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NOVITATES ZOOLOGICAE.
Vol. XXVII., 1920.
NOVITATES ZOOLOGICAE
H Journal of Zooloo\>
IN CONNECTION WITH THE THING MUSEUM.
EDITED BY
LORD ROTHSCHILD, F.R.S., Ph.D.,
Dr. ERNST HARTERT, and Dr. K. JORDAN.
Vol. XXVIL, 1920.
(WITH SEVENTEEN PLATES.)
Issued at the Zoological Museum, Trino.
PRINTED BY HAZELL, WATSON k VINEY, Ld., LONDON AND AYLESBURY.
1920.
CONTENTS OF VOLUME XXVII. (1920).
MAMMALIA
PAGES
1. A new Fat-tailed Gerbil (Pachyuromys) from Western Algeria. Oldfield
Thomas . . 313—314
2. Captain Angus Buchanan's Ah- Expedition. — 1. On a series of small
Mammals from Kano. Oldfield Thomas and Mabtin A. C. Hinton . 315 — 320
3. A note on Typo-locality and Geographical Races of the Gundi {('hnudactylus
gundi Rothm.). Oldfield Thomas ...... 506 — 507
AVES
1. The Birds of the Commander Islands. Ernst Haktert . 128 158
1. The Birds of Buckinghamshire and the Tring'Reservoirs (Plates XII. — XIII. ).
Ernst Hartert and Francis C. R. Jourdain .... 171 — 259
3. The new Names in J. Hermann's Tabula Affinitatum Animalium. Erwin
Stresemann ....... 327 332
4. Types of Birds in the Tring Museum. Ernst Hartert .... 425 — 505
COLEOPTERA
1. Some African Anthribidae. Karl Jordan ...... 260 264
LEPIDOPTERA
1. Supplemental notes to Mr. Charles Oberthiir's Fauno des Lepidopteres de la
Barbarie, with lists of the specimens in the Tring Museum (Plates XIV. —
XVII.). Lord Rothschild ........ 1 127
2. Notes on and Descriptions of Sphingidae (Illustrated). Karl Jordan . 159 — 162
3. The Status of Plalysphinx bourkei Trimen (1910). Karl Jordan . . 163 — 166
4. Some new African Sphingidae (Illustrated). Karl Jordan . . . 167 — 170
5. New Geometridae. Loots B. Prout ....... 265 — 312
PAOES
6. On the Genus Elachyophtkalma Feld. Lord Rothschild . 321 — 326
7. Sphingidae of Para (Plates I. — XI.). A. Miles Moss . . 333 — 424
8. Supplementary notes on Dioplidac. Louis B. Protjt .... 508 — 509
9. On some African Sphingidae. Kari, Jordan ..... 510 — 512
INDEX
513 — 544
LIST OF PLATES IN VOLUME XXVII.
I. — X. Caterpillars and Pupae of Sphingidae from Para. From drawings by A. Miles
Moss.
XI. Map of District of Para. By A. Miles Moss.
XII. Photograph of Grasshopper Warbler. By O. G. Pike.
XIII. Black-necked Grebe. By O. G. Pike.
XIV.— XVII. Lepidoptera from Algeria. By H. and E. S. Knight.
NOYITATES ZOOLOGICAE.
»a
H Journal of Zooloo\>-
EDITED BY
LORD ROTHSCHILD, E.R.S., Ph.D.,
Dr. ERNST HARTERT. and Dr. K. JORDAN.
Vol. XXVII.
No. 1.
Pages 1—332.
Plates XII., XIII.
Issued June 15th, 1920, at the Zoological Museum, Trijjg.
PRINTED BY HAZEIX, WATSON k VINEY, Ld., LONDON AND AYLESBURY.
1920.
Vol. XXVII.
NOVITATES Z00L0GICAE.
EDITED EV
LORD ROTHSCHILD, ERNST HARTERT, and KARL JORDAN
CONTENTS OF NO. I.
1. SUPPLEMENTAL NOTES TO MR. CHARLES
OBERTHUR'S FAUNE DES LEPIDOP-
TERES DE LA BARB ABIE, WITH LISTS OF
THE SPECIMENS IN THE TRING MUSEUM
(Pis. XIV.— XVII.).*— PART II. . . . Lord Rothschild .
2. THE BIRDS OF THE COMMANDER ISLANDS Ernst Hartert .
3. NOTES ON AND DESCRIPTIONS OF SPHIN-
GIDAE (Illustrated) Karl Jordan
4. THE STATUS OF PLATYSPHIXX BOURKEI
TRIMEN (1910) Karl Jordan .
5. SOME NEW AFRICAN SPHINGIDAE (Illus-
trated) Karl Jordan
6. THE BIRDS OF BUCKINGHAMSHIRE AND
THE TRING RESERVOIRS (Pis. XII., XIII.) Ernst Hartert and
Francis C. R. Jour-
dain
7. SOME AFRICAN ANTHRIBIDAE . . . Karl Jordan .
8. NEW GEOMETRIDAE Louis B. Prmtt .
9. A NEW FAT-TAILED GERBIL (PACHY-
VROMYS) FROM WESTERN ALGERIA . Oldfield Thomas
10. CAPTAIN ANGUS BUCHANAN'S AlR EX-
PEDITION.—I. ON A SERIES OF SMALL
MAMMALS FROM KANO .... Oldfield Thomas and
Martin A. C. Hinton
11. ON THE GENUS ELACHYOPHTHALMA
FELD Lord Rothschild
12. THE NEW NAMES IN J. HERMANN'S TABULA
AFF1MTATUM ANIMALWM . . Erwin Slresemann .
1-
-127
128-
-158
159-
-162
163—166
167-
-170
i ii-
-Z09
260-
-264
265—312
313-
-314
315—320
321—326
327—332
* Plates XIV.— XVII. will be issued with the next part.
NOVITATES ZOOLOGICAE
Vol. XXVH. JUNE 1920. No. I.
SUPPLEMENTAL NOTES TO MR. CHARLES OBERTHUR'S
FAUNE DES LEPIDOPTERES BE LA BARBARIE, WITH
LISTS OF THE SPECIMENS IN THE TRING MUSEUM.
{Continued from Vol. XXIV. p. 409 (1917).)
By Lord Rothschild, F.R.S., Ph.D.
(Plates XIV— XVII.)
THE long-expected volume of Mr. Oberthiir's Etudes de Lepidopterologie
Comparee, containing the Noctuidae of Algeria, has at last appeared. The
date on the wrapper is Octobre 1918, but the volume was only, received in
March 1919, so the date of publication for the new names published therein
must be taken as 1919.
It calls for various remarks. Mr. Oberthiir has adopted Guenee's system
of classification of the Noctuidae. Now, although the aim of Science is to establish
uniformity of nomenclature and a single classificatory system, it is impossible
to forbid the use of any system ; we can only regret, therefore, that such a
renowned entomologist as Mr. Oberthiir adopts systems and methods abandoned
by the majority of modern workers in Entomology. But while we can only
regret this retrograde policy of Mr. Oberthiir, we can and must strongly deprecate
the reasons he has and gives for not adopting Sir George Hampson's classification.
Whatever other objections Mr. Oberthiir may have to the British Museum classifica-
tion, he lays stress on one only, namely he harps upon the rather unfortunate
error made by Sir George Hampson in placing Phragmatobia breveti 0 berth, in
the genus Maenas. This error has long ago been acknowledged by its author.
Mr. Oberthiir makes great capital out of the aquatic habits of certain American
species of Maenas as opposed to the desert habitat of bzeveti, quite ignoring the
fact that the genus Maenas contains many African and Indo-Malayan species as
well as American, and these are, as far as we know, non-aquatic in their habits.
Sir George Hampson was misled by the somewhat aberrant neuration of P. breveti,
which is almost identical with that of Maenas ; moreover, breveti is not a Tricho-
soma as Mr. Oberthiir asserts, but a true Phragmatobia, The abortive wings of
the $ are not a generic character, but only specific, as can be seen in the case of
Cymbalophora rivularis Men., which has a 9 with abortive wings, while Cymba-
lophora pudica Esp. and C. oertzeni Led. have the $ full winged. The aquatic
habits of the larva are also only of secondary importance, for in the genus
Spilosoma (Diacrisia) we find Spilosoma (Diacrisia) metalhana with a free
swimming aquatic larva, while sannio and amurensis, which are very closely allied,
1
2 NOVITATES ZOOLOGICAE XXVII. 1920.
have ordinary terrestrial larvae. We cannot condemn a whole system simply
because its author made one rather striking error.
I have adopted the British Museum classification because so far there does
not appear to be a better one.
According to this classification, the family Noctuidae is divided into fifteen
subfamilies, viz. :
Agrotinae ; Hadeninae ; Cuculliinae ; Zenobiinae (Acronyctinae) ; Era-
striinae ; Phlogophorinae (Euteliinae) ; Odontoninae (Stictopterinae) ; Sarrothri-
pinae ; W ' ester manniinae (Acontiinae) ; Catocalinae ; Diphterinae (Mominae) ;
Phytometrinae ; Noctuituie ; Polypogoniiiae (Hypeninae) ; and Hyblaeinae ,
Of these fifteen subfamilies, two, namely, the Diphterinae and Hyblaeinael
have no representatives in Algeria, and three others, the Phologophorinae,
Odontoninae, and Sarrothripinae, have only one representative each.
Sir George Hanipson, who is a great stickler for classical correctness, in the
case of names forming subfamily appellations in which the ending is in "ia,''
insists on the subfamily being formed with the ending " ianae," such as
Cucullianaehom Cucullia. The International Rules, however, say the sub-family
term is to be made by the addition of the ending " inae " to the word, and so I
have made the families Cuculliinae, Zenobiinae, Erastriinae, and W estermanniinat
end in " iinae " instead " ianae."
I am taking the species, in the first place, in the order Mr. Oberthiir has
placed them in, for the purpose of critical remarks where these may be necessary ;
but at the end I am giving a full list of the species and genera in the order followed
by the British Museum classification. I am giving a list of the Algerian, Tunisian,
and Moroccan specimens in the British Museum as well as those at Tring.
1. Bryophila petrea Guen.
Bryophila petrea Guenee, Hint. Nat. Ins. Spec. Gen. Lipid, vol. v. Noct. vol. i. p. 25. No. 22 (1852)
(Andalusia).
Mr. Oberthiir records this species from Maafa and Lambessa ; we have
received 35 from Guelt-ea-Stel, 1 from Batna, and 1 El Kantara.
There are in the Tring Museum 18 (J <$, 17$$ from Guelt-es-Stel. This series
shows considerable variation in the forewings, some being pale grey with hardly
any markings, while others are of a deeper brighter grey with conspicuous black
markings, and a few have such dark grey forewings that the black markings
show up hardly darker than the ground colour.
1 ^Environs de Batna, 1914 (A. Nelva) ; 1 cj El Kantara, August 1917 (V.
Faroult).
2. Bryophila aerumna Culot.
Bryophila aerumna Culot, Xoct. et Gtom. d'Eur. pt. i. vol. i. p. 131, pi. 22. f. 17 (1912) (Giryville).
Monsieur Culot quotes this and a number of other new species as "Oberth."
because he adopts the names suggested by Mr. Oberthiir in his letters to him ;
while Mr. Oberthiir quotes them as "Culot (secundum Oberthiir)." Both these
methods are wrong ; the correct way of quoting is Bryophila aerumna Culot ;
but if it is thought desirable to mention Mr. Oberthur's connection with these
species, it should be done as follows: Bryophila aerumna Culot (Oberth. in lilt.)
NOVITATES ZOOLOGICAE XXVII. 1920. 3
There are at Tring 32 specimens of this species from Sidi-bel- Abbes, September
1917 (M. Rotrou) ; Sebdou, September 1918 (P. Rotrou) ; Perregaux, September
1915 (V. Faroult) ; AIn Draham, September 1911 (V. Faroult).
[Bryophila aeton Culot = Catamecia mauretanica Stdgr.
Calamecia jordana var. mauretanica Staudinger and Rebel, Cat. Lepid. Pal. Faun, pt. i. p. 213. No
2192i) (1901) (Biskra).
Bryophila aeton Culot, Noct. el Gtom. d'Eur. pt. i. vol. i. p. 132. pi. 22. f. 16 (1912) (El Outaya).
Neither Mr. Oberthiir nor Mr. Culot have perceived that the type of aeton
is only a heavily marked fine specimen of Catamecia mauretanica Stdgr.]
3. Bryophila divisa oxybiensis Mill.
Bryophila oxybiensis Milliere, Rev. Zool. 1874, p. 242 (Cannes).
Catamecia bryophiloides Rothschild, Novit. Zool. vol. xxi. p. 330. No. 194 (1914) (Guelt-es-Stel).
The name divisa has one year's priority over that of pomula ; Esper being
1791, while Borkhausen is 1792. Pere Engramelle, it is true, is older, but he has
" La Pomule " not pomula, so the date of pomula is that of Borkhausen, who
latinised Pere Engramelle's name.
In 1913 (Novit. Zool. vol. xx. p. 125, No. 52) I unfortunately identified
some unicolorous grey specimens of this insect from the Oued Nca as Bryophila
pineti Stdgr., which I then only knew from a drawing. I have now discovered this
error, and I name these unicolorous specimens ab. unicolor ab. nov. The form of
divisa oxybiensis most similar in coloration to typical divisa must bear the name
ab. rufilincta Rothsch. (Novit. Zool. vol. xx. p. 125 (1913)), and the form with
the basal two-thirds of the forewing below median fold black is ab. distincta
Rothsch., and, lastly, the very dark form ab. saturatior Rothsch., both described
on p. 125.
We have at Tring 1 Hammam R'hira June 1916, 1 Alger January 1914
(V. Faroult) ; 27 c?c?, 21 $$ Oued Kca, June 1912 (E. H. and C. H.) ; 5 <?<?, 2 $$
Guelt-es-Stel, August - September 1913 (V. Faroult) ; 4 <?£, 2 $$ Ain Sefra,
June— July 1915 (V. Faroult) ; 4 S3, 1 $ Les Pins, September 1918 (M. Rotrou) ;
1 $ Sidi-bel-Abbes, July 1916 (M. Rotrou); 1 $, 1 $ Sebdou, July 1918 (P.
Rotrou) ; 1 cJ Glacieres de Blida, June 1908 (W. R. and K. J.). Of the Ain
Sefra specimens 1 is ab. r u fit i acta and 1 the form of oxybiensis described by
Staudinger as ab. striata, as is the Blida <J.
In Novit. Zool. vol. xxi. I described 3 specimens from Guelt-es-Stel as
Catamecia bryophiloides. These 3 (1 <J, 2 $$) are smaller than the 4 other Guelt-
es-Stel specimens, the wings are narrower, they are of a brown-grey colour, and
have almost obsolete markings. Both Sir George Hampson and Dr. Jordan, who
have re-examined these specimens, consider they are only an extreme aberration
of d. oxybiensis, with which I must agree. Therefore bryophiloides sinks as a
synonym of divisa oxybiensis. The Tring series thus totals 70 specimens.
4. Bryophila simulatricula Guen.
Bryophila simulatricula Guenee, Hist. Nat. Ins. Spec. Gin. Lepid. vol. v. Noct. vol. i. p. 2fi. No. 24
(1852) (Florence).
There has been considerable difference of opinion concerning the status of
this insect. When Sir George Hampson wrote vol. vii. of his catalogue, he
i Novitates Zoolooicae XXVII. 1920.
considered it the same as palliola Borkh. = fraudatricula Hiibn., and Mr.
Oberthiir appears to be of the same opinion. Sir George has, however, now come
round to the opinion that it is a distinct species owing to the breeding of simu-
latricula and palliola from the egg by Herr Piingler and some of his friends.
I do not agree at all with Mr. Oberthiir. nor does Sir George Hampson, that my
albomaculata = albimacula Oberth. has anything to do with true simulatricula,
of which I have four specimens from Guelt-es-Stel and Ain Sefra agreeing very well
with European specimens.
2 ?? Guelt-es-Stel June-July 1913, 1 3, 1 $ Ain Sefra June 1915 (V.
Faroult) ; in the Tring Museum.
5. Bryophila albomaculata albomaculata Rothsch.
Bryophila albomaculata Rothschild, Novit. Zool. vol. xxi. p. 333. No. 178 (1914) (Guelt-es-Stel).
Bryophila simulatricula albimacula Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 9. pi. xd. f. 4033 (1919)
(Batna).
There are two distinct races of this insect in Algeria, the typical form from
East and Central Algeria, which is paler grey more or less washed with yellow,
and a darker grey race with no yellow wash from West Algeria.
There are at Tring of the typical form : 1 £, 5 $$ Guelt-es-Stel, September
1913 (V. Faroult) ; 3 ?? Batna (Nelya coll.) ; 2 $$ Metlili, S. of Laghouat,
September 1917 (V. Faroult).
6. Bryophila albomaculata grisescens subsp. nov.
Differs from a. albomaculata in the darker grey of the forewings with no trace
of yellow wash. The reniform stigma is generally white, but not always.
6 <J<J, 5 ?$ Sebdou, September 1918 (P. Rotrou) ; 1 <J, 3 $$ Les Pins,
September 1918 (M. Rotrou).
7. Bryophila algae (Fabr.).
Noctua algae Fabricius, Syst. Entom. p. 614. No. 103 (1775) (Germany).
It is rather strange that I have received so few specimens of this species, which
is very abundant in Algeria.
1 (J, 1 ? Sidi-bel-Abbes, September 1917 (M. Rotrou) ; 1 <J, 1 ? Environs de
Batna, 1911-1912 (Nelva coll.) ; 1 ^ Les Pins, August 1918 (P. Rotrou) ; 1 <J
Ain Draham, September 1911 (V. Faroult); 4 <$<S, 2 $? Rabat, Morocco (A.
Thery) ; 1 $ El Mahouna, September 1919 (V. Faroult).
8. Bryophila galathea Mill.
Bryophila galathea Milliere, Rev. Zool. 1874. p. 241 (Cannes).
This species appears to be very rare in Algeria, as I have only a single example.
1 ? Ain Sefra, May 9, 1913 (W. R. and E. H.).
9. Bryophila bilineata Rothsch.
Bryophila bilineata Rothschild, Novil. Zool. vol. xxi. p. 333. No. 179 (1914) (Guelt-es-Stel).
Bryophila rosinans Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 10. pi. xd. Nos. 4034-4037 (1919)
(Gervville).
This species = rosinans Oberth. and has five years' priority. It is quite
distinct from ravula Hiibn.
Novitates Zoolooicae XXVII. 1920. 5
There are at Tring 84 specimens, Guelt-es-Stel, August— September 1913
(V. Faroult).
10. Bryophila ravula (Hiibn.).
Noctua ravula Hiibner, Eur. Schmett. Noel, f. 461 (1818) (Europe).
There are 84 specimens of this species at Tring from A'in Draham, August —
September 1911 (V. Faroult); Sidi-bel-Abbes, September 1917 (M. Rotrou);
Sebdou, September 1918 (P. Rotrou) ; Foret de Tenira, September 1918 (P.
Rotrou) ; Perregaux, September 1915 (V. Faroult) ; north side of Djebel Zaccar,
August 1910 ( V. Faroult) ; Environs de Taourirt, Morocco, July 1918 (M. Rotrou).
11. Bryophila anaemica Hmpsn.
Bryophila anaemica Hampson, Ann. Mag. Nat. Hisl. (8) xiii. p. 156. No. 3527« (1914) (Batna).
This species was described from a very worn specimen ; it is quite probable
that it is an extreme aberration of albomaciilata albomaculala, but as my <J is
quite fresh and is very different from that species, I keep it separate.
1 $ Batna (Nelva coll.).
1 cJ type Batna, August 1910 (A. E. Eaton coll.) in British Museum.
12. Bryophila receptricula pallida B. Baker.
Bryophila pallida Bethune Baker, Trans. Enlom. Soc. Lond. 1894. p. 37. pi. 1. f. 4 (Alexandria).
The Algerian specimens, though very variable, are all referable to the form
pallida.
There are 108 specimens at Tring : 49 Sidi-bel-Abbes, September - October
1917 (M. Rotrou); 3 Les Pins, September 1918 (M. Rotrou); 3 Sebdou,
September 1918 (P. Rotrou) ; 1 Messer, Prov. Oran, September 1917 (M. Rotrou) ;
1 Perregaux, September 1915 (V. Faroult) ; 13 Foret de Tenira, September 1918
(P. Rotrou); 2 Environs de Batna, 1911-1912 (Nelva coll.); 7 Ain Draham,
September 1911 (V. Faroult); Rabat, Morocco, July— August 1913 (A. Thery) ;
Messen, September 1917 (M. Rotrou) ; 2 El Mahouna, July— September 1919
(V. Faroult).
13. Bryophila antias Culot.
Bryophila antias Culot, Noel, el Giom. d'Eur. pt. i. vol. i. p. 134. pi. 22. f. 13 (1912) (Sud Oranais).
3 $$ are at Tring: Sebdou, September 1918 (M. Rotrou); Guelt-es-Stel,
August 1913 (V. Faroult).
14. Bryophila pseudoperla Rothsch.
Bryophila pseudoperla Rothschild, Novit. Zonl. vol. xxi. p. 334. No. 180 (1914) (Guelt-es-Stel).
The $ type remained unique till 1919.
1 $ Guelt-es-Stel, 4 J J, 1 $ Metlili, S. of Laghouat, September 1917
(V. Faroult).
15. Bryophila muralis (Forst.).
Pkalaena muralis Forster, Nor. Spec. Ins. p. 74 (1771) (England).
Both muralis and the form par accur in Algeria as well as extreme forms
like par, but with no vestige of green tint.
6 NOVITATES ZOOLOGICAE XXVII. 1920.
Of the form muralis there are at Tring 16 specimens from Tunis ; Am Draham,
August 1911, north side of Pjebel Zaccar, August 1916 (V. Faroult) ; Environs
de Batna (Nelva coll.) ; Sidi-bel-Abbes, July -.September 1917 (M. Rotrou) ; Les
Pins, August 1918 (M. Rotrou); Sebdou, July -September 1918 (P. Rotrou);
Foret de Tenira, September 1918 (P. Rotrou). Of the form par and extremes,
there are at Tring 8 specimens from Hussein Bey, May (Captain Holl) ; Sidi-
bel-Abbes, August -September 1916-1917 (M. Rotrou).
16. Oederemia precisa (Warr).
Metachrostis precisa Warren in Seitz Grossschm. Erde, vol. iii. p. 23 (1909) (Mazagan).
Jugurthia sabnonea Culot, Noel, et Geom. d'Eur. pt. i. vol. i. p. 124. pi. 22. f. 12. (1912) (Zebch. nr.
Sebdou).
Catamec.ia subperla Rothschild, Novit. Zool. vol. xxi. p. 336. No. 195 (1914) (Guelt-es-Stel).
The genus Jugurthia was founded by Monsieur Culot (Noct. et Geom. d'Eur.
p. 124) to receive the 3 species microglossa, salmonea = qrrecisa, and subplum-
beola, and consists of the mixture of the two genera of Sir George Hampson
Oederemia {Cat. Lep. Het. Brit. Mus. vol. vii. p. 405) type lithopasta Hmpsn. and
Oedibrya founded on cinnomomina Rothsch. = subplumbeola Culot. As Oederemia
antedates Jugurthia by four years, M. Culot's genus becomes a synonym. Mr.
Warren's specific name precisa antedates salmonea by three years, and therefore
both Mr. Culot's name and my subperla also become synonyms.
There are at Tring, including the types of precisa and subperla, 347 specimens
from Mazagan, Morocco, September— October 1902 (W. Riggenbach) ; Lalla
Marnia, Oran, September— October 1914 (V. Faroult); Sebdou, September 1918
(P. Rotrou); Merchich, Oran, September 1918 (P. Rotrou); Perregaux, October
1915 (V. Faroult); Sidi-bel-Abbes, September— October 1917 (M. Rotrou);
Guelt-es-Stel, August— October 1913 (V. Faroult).
This insect is extremely variable in ground-colour, varying from brown-grey
to cinnamon-orange.
1 <J, 1 9 in the British Museum (Guelt-es-Stel, received from Tring Museum).
17. Oedibrya subplumbeola (Culot).
Jugurthia subplumbeola Culot, Noct. et Gtom. d'Eur. p. 125. pi. 22. f. 14 (1912) (Geryville).
Catamecia cinnamomina Rothschild, Xovit. Zool. vol. xxi. p. 336 (1914) (Guelt-es-Stel).
When I wrote my paper on the Guelt-es-Stel lepidoptera I had not got
Mr. Culot's book, which accounts for my redescribing this insect. It is tolerably
widely spread in Algeria, though nowhere very common.
We have at Tring 29 specimens, including the types of cinnamomina and
the aberrations suffusa, griseola, and fasciata, tl.e latter = ab. precisa Culot, from
Guelt-es-Stel, September 1912-1913 (V. Faroult) ; Sidi Ferruch (A. Thery) ;
Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Sebdou, September 1918 (P.
Rotrou) ; Les Pins, September 1918 (M. Rotrou) ; Aflou, September— October
1916 (V. Faroult) ; Lambessa, 1914 (Nelva coll.).
18. Pseudamathes volloni (D. Lucas).
Amathes volloni Daniel Lucas, Bull. Soc. Entom. France, 1907. p. 342 (Kebili).
This species was described from South Tunisia, and placed originally by
Sir George Hampson in the genus Amathes. There are two specimens in the
Novitates Zoolooicae XXVII. 1920. 7
British Museum, and on more careful examination they prove to belong to a new
genus Pseudamathes, which comes next to Pseudohadena in the Zenobiinae. It
appears to be rare in Algeria, as I have only received a single cj from Aflou,
October 10th, 1916 (Victor Faroult).
19. Craniophora pontica (Stdgr.).
Acronycta pontica Staudinger, Hor. Soc. Entom. Ross. vol. xiv. p. 364 (1879) (KerasdereV
This insect is fairly abundant in Algeria. We have at Tring 58 specimens
from Sebdou, May— June 1918 (P. P.otrou) ; Hammam R'hira, May— June 1916-
1917 (V. Faroult) ; Sakamodi, August 1912 (V. Faroult) ; Hammam Meskoutine,
April 1914 (W. R. and K. J.) ; Batna, July 1912 (Nelva coll.) ; Am Draham
August — September 1911, north side of Ljebel Zaccar August 191G, Environs
deSetif 1911 (Victor Faroult).
Monsieur Oberthur says that his specimens from Sebdou are suffused with
pink ; the few I have from there have no pink shade and are very dark.
20. Acronycta tridens (Schiff. & Den.).
Noct'ia tridens Schiffermiiller and Denis, Ank. Syst. Work. Schmett. Wienergeg. p. 67 (1775) (Vienna),
We have at Tring 11 JcJ, 15 $$ from Ain Draham, July —September 1911
(Victor Faroult) ; Bou Saada, March— May 1912 (V. Faroult); Batna (Nelva
coll.) ; Environs de Setif, 1911 (V. Faroult) ; Hammam Meskoutine, April 1914
(W. II. and K. J.) ; 2 Jd Hammam R'hira, May 1917 (V. Faroult).
21. Acronycta psi (Linn.).
Phalaena psi Linnaeus, Syst. Nat. edit. x. p. 514 (1758).
This species is not recorded from Algeria by Mr. Oberthur nor Mr. Culot.
It was bred on cherry trees by Mr. M. Rotrou.
We have 6 cjcS, 5 $$ (1 cripple) from SidiJoel-Abbes, Messer, and Ain Fezza,
May— September 1917 (M. Rotrou).
22. Acronycta rumicis pallida subsp. nov.
Differs from r. rumicis in being distinctly paler, but not so pale as rumicis
ttiranica Stdgr. M. Oberthur has noticed the paler coloration, but did not give
the Mauretanian form a name.
We have at Tring 126 specimens from SidiJjel-Abbes, May — October 1917-
1918 (M. Rotrou); Hammam R'hira, May— August 1916 (Victor Faroult);
Environs de Setif, 1911 (V. Faroult); Batna, July 1912 (Nelva coll.); Ain
Draham, July— September 1911 (V. Faroult).
In the British Museum 1 $, Tangier, Juty 1902, Lord Walsingham.
23. Copicucullia oberthuri (Culot).
Simyra oberthuri Culot, Noct. et Giom. d'Eur. pt. i. vol. i. p. 26. pi. 3. f. 1 (1909) (Aflou).
Both Mr. Oberthur and Mr. Culot have placed this insect in the genus Simyra,
with which it has nothing to do. It certainly has a slight resemblance to Simyra
8 NOVITATES ZOOLOGICAE XXVII. 1P20,
dentinosa Frr., but it is a true Cucullid, and in spite of its pectinated antennae
belongs with cyrtana Mab. to the genus Copicvcvllia.
We have at Tring 181 specimens of this insect from Guelt-es-Stel October
1912- November 1913, Hassi Baba November 1917 (Victor Faroult). There are
3 (JcJ (Guelt-es-Stel, October 1912) in the British Museum ex Tring Museum.
24. Lycophotia mansoura (Chret.).
Agroti-j mansoura Chretien, Ann. Soc. Enlom. France, vol. 79. p. 498 (1910) (Gaisa).
I have this species from Guelt-es-Stel in some numbers. The general run oi
the specimens appear to have less sharply defined markings than is stated in Mr.
Chretien's description. This insect is placed by Mr. Oberthiir in the genus
Simyra, but it has not the remotest relationship with that genus : it is a true
Agrotid, and together with the following species belongs to the genus Lycophotia
of the subfamily Agrotinae, while Simyra is a genus of the Zenobiinae (Acronyctinae).
There are at Tring 149 specimens from Guelt-es-Stcl, October 1912
(V. Faroult).
25. Lycophotia agrotina (Rothsch.).
Actinotia agrotina Rothschild, Novit. Zool. vol. xxi. p. 31G. No. CI (1914) (Guelt-es-Stel).
This species differs from mansoura in its much broader wings and more
accentuated marking ; it is figured in vol. xxvi. pi. i.
There are at Tring, including the type, 23 cJcJ, 3 ?$ from Guelt-es-Stel, October
1912 (V. Faroult).
26. Simyra autumna Chret.
Simyra autumna Chretien, Ann. Soc. Entom. France, vol. 79. p. 497 (1910) (Gafsa).
This appears to be the only true Simyra occurring in Mauretania ; it is nearest
to dentinosa Frr.
I have not received this species, nor have I ever seen a specimen.
Mr. Oberthiir mentions it after Sesamia crelica, having evidently added it
as an afterthought.
27. Argyrospila musculosa (Hiibn.).
2\oetua musculosa Hiibner, Europ. Schmett. Noel. f. 363 (1808).
I recorded vol. xxi. p. 337, No. 198, Oria myodea Ramb. The specimen was
very greasy and turns out to be a very heavily marked musculosa.
We have at Tring 396 Mauretanian specimens from Environs d'Alger, May
1908, etc. (W. R. and K. J., Dr. Nissen and Captain Holl) ; Batna (Nelva coll.) ;
Tunis; Guelt-es-Stel, May— June 1913 (V. Faroult); Hammam Meskoutine,
May 1914 (W. R. and E. H.) ; Khenchela, June 1911 (V. Faroult) ; El Kantara,
June 1911 (V. Faroult) ; Sidi-bel-Abbes, June 1917 (M. Botrou) ; Zmila, Prov.
Oran, June 1913 (V. Faroult) ; Sebdou, June 1918 (P. Rotrou) ; Foret de Tenira.
May 1918 (P. Rotrou) ; Masser Mines May 1914, Lalla Marnia May 1914 (V.
Faroult); Hammam R'hira, May 1913 (W. R. and E. H.); Hammam R'hira,
May 1916 (V. Faroult) ; El Mesrane, June 1913 (V. Faroult) ; El Hamel, May
1912 (V. Faroult); Bou Saada and Djebel Kerdada, May 1912 (V. Faroult);
Novitates Zoological XXVII. 1920. 9
Terres Blanches, May 1913 (V. Faroult) ; Foret de Djelfa, June 1913 (V. Faroult) ;
El Mahouna, June— July 1919 (V. Faroult).
28. Sideridis lithargyria argyritis (Ramb.).
Leucania argyritis Rambur, Cat. Syst. Lipid. Andal. pi. 8. f. 2 (185S) (Andalusia).
Mr. Oberthiir considers this insect a distinct species from lithargyria, but it is
the general consensus of opinion that it is the Mediterranean subspecies of that
species.
The Tring Museum possesses 77 specimens from Sidi-bel-Abbes, September
1916-1917 (M. Rotrou) ; Sebdou September 1918, and Foret de Tenira August
1918 (P. Rotrou) ; Environs de Sctif, 1911 (V. Faroult) ; A'in Draham, August-
September 1911 (V. Faroult).
29. Sideridis albipuncta (Schiff. & Den.).
Noctua albipuncta Schiffermuller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 84 (1775)
(Vienna).
Not so abundant as vitellina, but very plentiful in certain localities.
The Tring series from Mauritania, consists of 160 specimens from Sidi-bel-
Abbes, September— October 1917 (M. Rotrou); Sebdou, June 1918 (P. Rotrou) ;
Foret de Tenira, June— July 1918 (P. Rotrou) ; Les Pins, July 1918 (M. Rotrou) ;
Environs de Setif and Oued Hamidou, June 1912 (V. Faroult) ; Khenchela, May
1912 (W. R. and K. J.) ; Blida, March 1916 (V. Faroult) ; Hammam R'hira,
April— August 1912-1916 (W. R., E. H. and K. J., and V. Faroult) ; Masser Mines
June 1914, north side of Djebel Zaccar August 1916 (V. Faroult) ; El Mahouna,
June— September 1919 (V. Faroult).
30. Cirphis sicula (Treit.).
Leucania sicula Treitschke, Schmett. Eur. vol. x. pt. 2. p. 90 (1835) (Sicily).
This species varies considerably in the amount of black along the median
vein and fold, and also in the size and distinctness of the black and white dis-
cocellular stigma.
We have at Tring 143 Mauretanian specimens from Sidi-bel-Abbes,
September 1917 (M. Rotrou); Sebdou and Foret de Tenira, September
—October 1918 (P. Rotrou) ; Masser Mines, June 1914 (V. Faroult) ; Mazagan,
Morocco, March 1902 (W. Riggenbach) ; Guelt-es-Stel, April— October 1912-
1913 (V. Faroult) ; Hammam R'hira, May 1908-1916 (V. Faroult, and W. R.
and K. J.) ; Hammam Meskoutine, April— May 1914 (W. R. and K. J.) ;
Batna, May 1915 (Nelva coll.) ; Biskra, April 1908 (W. R. and E. H.) ; Environs
d'Alger, May 1908 (W. R. and K. J., and Captain Holl) ; Souk Ahras, April 1914
(W. R. and K. J.) ; Ai'n Braham August— September 1911, north side of Djebel
Zaccar August 1916 (V. Faroult) ; Belvedere, Tunis, August —September 1915
(M. Blanc) ; El Mahouna, September 1919 (V. Faioult).
The extreme form with heavy black colouring along median vein and fold
is very similar to the insect described by Bellier de la Chavignerie (Ann. Soc.
Entom. France, ser. 4, vol. iii. p. 42, pi. ix. f. 5 (1863)) as Leucania hispanica,
which Sir George Hampson has placed as a synonym of Cirphis prominent; (Walk.).
Mr. Oberthiir treats the dark Algerian sicula as hispanica, but I have not yet seen
a true hispanica from Algeria.
10 Novitates Zoolooicae XXVII. 1920.
[Cirphis fuscilinea (Grasl.).
Leucania fuscilinea Graslin, Ann. Soc. Entom. France, ser. 2. vol. 10. p. 41 1. pi. 8. i. f. 2 (1852) (France).
I cannot agree with Mr. Oberthur and Sir George Hampson that this is a
synonym of sicula. The strongly marked post-median curved line of black spots
is not present in a single one of my 120 Algerian, etc. sicula, nor in 12 European
ones I have ; and my solitary Central Italian fuscilinea stands out most plainly
from all the 132 in this character.]
31. Leucania languida Stdgr.
Leucania languida Staudinger, Iris, vol. x. p. 284. pi. ix. f. 16 (1897) (Jordan Valley).
Mr. Oberthur records a single specimen from Biskra. I have never had
one from Mauretania.
32. Cirphis algirica (Oberth.).
Leucania algirica Oberthur, Etud. Lepid. Comp. fasc. xvi. p. 19. pl.xd. ff. 4045, 4046(1919) (Batna).
I have received 43 specimens of this species, 16 from Sidi-bel-Abbes, June
—September 1917 (M. Rotrou) ; and 2 from A'in Sefra July 1915, Hammam
R'hira June 1917 (V. Faronlt) ; Foret de Tenira, October 1918 (P. Rotrou).
33. Cirphis punctosa (Treit.).
Siinyra punctosa Treitschke, Schmett. Eur. vol. v. pt. 2. p. 287 (1825) (S. France).
We have at Tring 250 Mauretanian specimens, 181 Guelt-es-StoI, August —
October 1912-1913 (V. Faroult) ; and 53 from Sebdou and Foret de Tenira,
September 1918 (P. Rotrou) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Les
Pins, September 1918 (M. Rotrou); Perregaux October 1915, Aflou October
1916 (V. Faroult) ; Batna, 1913-1914 (Nelva coll.) ; El Mahouna, September
1919 (V. Faroult).
34. Cirphis putrescens (Geyer).
Noctua putrescens Geyer in Hiibner, Samml. Eur. Schmett. Xoct. ff. 730-731 (1827).
We have 392 specimens at Tring from Guelt-es-Stel, August — September
1913 (V. Faroult) ; Sebdou and Foret de Tenira, September 1918 (P. Rotrou) ;
Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Aflou October 1916, Perregaux
October 1915, Metlili, S. of Laghouat, September 1917 (V. Faroult).
35. Cirphis loreyi (Dup.).
Noclua loreyi Duponchel, Lepid. France, vol. vii. p. 81. pi. 105. I. 7 (1827) (France).
The Mauretanian series at Tring consists of 116 specimens from Sidi-bel-
Abbes, August — October 1917 (M. Rotrou) ; Sebdou and Foret de Tenira, June -
July 1918 (P. Rotrou) ; Perregaux, October 1915 (V. Faroult) ; Aflou, October
1916 (V. Faroult) ; Guelt-es-Stel, September 1912— June 1913 (V. Faroult) ;. Le
Kreiden (M. Rotrou) ; Masser Mines June 1914, Batna 1911-1912 (Nelva coll.) ;
Tilghemt April 1912, El Kantara August 1917 (V. Faroult); El Golea, March
1912 (Hartert and Hilgert) ; Biskra, March 1908-1911 (W. R, and E. H., V.
Faroult) ; Environs de Setif, 1911 (V. Faroult) ; Oued Hamidou June 1912, Ain
NOVITATES ZOOLOQICAE XXVII. 1920. 11
Draham July 1911 (V. Faroult) ; Bou Saada, April 1912 (V. Faroult) ; Ham-
mam R'hira, May 1913 (W. R. and E. H.) ; Environs d'Alger (Captain Holl and
Dr. Nissen) ; El Mahouna, June 1919 (V. Faroult).
In the British Museum are 1 $ Central Plains, Morocco, June 1901, Meade
Waldo ; 1 <J Biskra, December 1896, A. E. Eaton.
36. Cirphis 1. album (Linn.).
Phalaena I. al'mm Linnaeus, Syst. Nat. edit. xii. p. 850 (1767) (Europe).
The Mauretanian series at Tring consists of 130 specimens from Environs
d'Alger, February -.May 1908 (W. R., E. H., and K. J.) ; Hammam R'hira, May
1908 -June 1916 (W. R., E. H, and K. J., and V. Faroult) ; Guelt-es-Stel, April-
October 1913 (V. Faroult) ; Laghouat, April 1911 (W. R. and E. H.) ; Blida les
Glacieres, June 1908 (W. R. and K. J.); Biskra, February —April 1908-1911
(W. R. and E. H.) ; Environs de Batna, April -August 1912-1914 (Nelva coll.) ;
Lambessa, July 1912 (Nelva coll.) ; Khenchela, May 1912 (W. R. and K. J.) ;
Ain Draham, August —September 1911 (V. Faroult); Perregaux, October 1915
(V. Faroult) ; Masser Mines, June 1914 (V. Faroult) ; Messer, September 1917 (M.
Rotrou) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Foret de Tenira, June —
August 1918 (P. Rotrou) ; Sebdou, May 1918 (P. Rotrou); Aflou, October 1916
(V. Faroult) ; Bou Saada, March— April 1911 (Victor Faroult).
37. Cirphis congrua (Hiibn.).
Noctwi congrua Hiibner, Samml. Europ. Schmett. Noct. f. 616 (1827).
This appears to be very rare in Algeria, as Mr. Oberthiir only received 1 and
I have only 3 specimens.
1 $ Hammam R'hira, August 28th, 1916 (V. Faroult); 1 ^ Hammam
Meskoutine, April 1914 (W. R. and K. J.) ; 1 $ Sidi-bel-Abbes, October 1917
(M. Rotrou).
38. Sideridis vitellina (Hiibn.).
Noctwi viteUina Hiibner, Samml. Europ. Sclvnett. Noct. ff. 379, 5->9 (1827).
Both Warren's ab. pallida and my Borolia lacteicolor are the pale form of this
insect. It is strange that this pale form is almost invariably smaller than the
darker more strongly marked typical form.
The series of Mauretanian examples at Tring consists of 319 specimens, 218
typical vitellina and 101 ab. pallida Warr. from Environs d'Alger, May 1908
(W. R., E. H., and K. J.) ; Blida les Glacieres, June 1908 (W. R. and K. J.) ;
Khenchela, May 1912 (W. R. and K. J.) ; Hammam Meskoutine, April 1914
(W. R. and K. J.) ; Hammam R'hira, May— June 1908-1913 (W. R., E. H., and
K. J.) ; Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and V. Faroult) ;
Batna, September 1910 — August-September 1912 (Nelva and V. Faroult); Bou
Saada, April— May 1912 (V. Faroult); Oran, April 1913 (W. R. and E. H.) ;
Sidi-bel-Abbes, May 1918 (M. Rotrou) ; Ain Sefra, May 1913 (W. R. and E. H.);
Foret de Tenira, June 1918 (P. Rotrou) ; Sebdou, May 1918 (P. Rotrou) ; Titen
Yaya, May 1915 (M. Rotrou) ; Messer, September 1917 (M. Rotrou) ; Am Draham,
August— September 1911 (V. Faroult); Environs de Setif, 1911 (V. Faroult);
El Mahouna, September 1919 (V. Faroult).
12 NOTITATES ZOOLOQICAE XXVII. 1920.
39. Cirphis riparia (Ramb.).
Leucania riparia Rambur, Ann. Soc. Obs. 1829. p. 261. pi. 6. f. 6.
I have 8 Mauretanian examples of this species from Moroccan Frontier ; 15
km. west of Lalla Marnia, May 1914 (V. Faroult) ; A'in Sefra, May 1915 (V.
Faroult) ; Batna (Nelva coll.) ; Sidi-bel-Abbes, September 1917 (M. Rotrou).
Not recorded by Mr. Oberthiir.
40. Cirphis zeae (Dup.).
Noctva zeae Duponchel, Lipid. France. T. vii. {Noel. vol. 4. pt. 1) p. 363. pi. 122. f. 4 (1827) (France).
This species is not mentioned by Mr. Oberthiir.
The Mauretanian series at Tring consists of 13 specimens from Sidi-bel-Abbes,
August— October 1917 (M. Rotrou) ; and 1 $ Foret de Tenira, August 1918
(P. Rotrou).
41. Cirphis unipuncta (Haw.).
Noctva unipuncta Haworth, Lipid. Brit. p. 174 (1809) (Great Britain).
This is also not mentioned by Mr. Oberthiir.
1 (J Am Draham, August 1911 (V. Faroult); 1 ? Sidi-bel-Abbes, October
1917 (M. Rotrou).
42. Leucania obsoleta (Hiibn.).
Noctua ohsolcta Hiibner, Samml. Europ. Schmett. Noct. i. 233 (1827).
Mr. Oberthiir has not recorded this species.
1 $ Batna, July 1912 (Nelva coll.).
43. Sesamia vuteria (Stoll).
Phalaena vuteria Stoll, Suppl. Cram. Pap. Exot. p. 161. pi. 36. f. 5 (1783) (Cape Colony).
Mr. Oberthiir records this species under Lefebre's name of nonagrioides, the
date of which is 1827. I have received only females of vuteria.
We have at Tring 10 $$ from Sidi-bel-Abbes, May— September 1917-1918
(M. Rotrou) ; Sebdou and Foret de Tenira, September 1918 (P. Rotrou) ; Blida,
March 1916 (V. Faroult) ; Oued Hamidou, June 1912 (V. Faroult).
In the British Museum are 1 (J, 1 $ Algeria, Mrs. Nicholl and Leech coll. ;
1 $ Hammam-es-Salahin, March 1904, Lord Walsingham.
44. Sesamia cretica Led.
Sesamia cretica Leilerer, Noct. Europ. p. 225 (1857) (Crete).
Mr. Oberthiir only records by name 2 species, but throws out a hint that
Staudinger's var. et ab. striata is probably a distinct species ; my series not only
shows this to be the case, but I have also a fourth species calamistis Hmpsn. I
only have 8 typical cretica.
1 <J, 2 ?$ Sidi-bel-Abbes, June 1916-1917 (M. Rotrou) ; 1 ? (dwarf) Perregaux,
September 1915 (V. Faroult) ; 2 $$ Sebdou, July— September 1918 (P. Rotrou) ;
1 £ Ain Draham, September 1911 (V. Faroult).
NOVITATES ZOOLOOICAE XXVII. 1920. 13
45. Sesamia striata Stdgr.
Sesamia crelica var. et ab. striata Staudinger, Slett. Ento-n. Zeit. 188S. p. 27 (Fergana).
1 have 2 $£, 3 $$, all of which are much paler than cretica, show no trace of
pink ground-colour, and all have the dark median band from base to termen.
2 (J(J, 3 $? from Sidi-bel-Abbes, June 1916-1917 (M. Rotrou) ; Sebdou and
Foret de Tenira, June — July 1918 (P. Rotrou) ; Ain Draham, August — September
1911 (V. Faroult).
4(3. Sesamia calamistis Hmpsn.
Sesamia calamistis Hampson, Cat. Lepid. Phal. Brit. Mus. vol. ix. p. 325. No. 4754. pi. cxliv. f. 18
(191U) (Grahanistown).
This species, like vuteria, was first described from South Africa, and evidently
like that species has a much larger range than we at first suspected. The 3
specimens sent by Mr. Rotrou are quite typical.
1 <J, 2 ?$ Sidi-bel-Abbes, September 1917 (M. Rotrou).
47. Argyrospila striata Stdgr.
Argyrospila striata Staudinger, Iris, vol. x. p. 265. pi. I. f. 4 (1897) (CheUala).
Two insects have been mixed up under this name by subsequent authors,
viz. Timora albida Hmpsn. and the present species. This has been caused by
both species having longitudinal white streaks on the forewings, and nobody
having both species until we collected them.
The Tring Museum series consists of 317 specimens from Guelt-es-Stel May
1913, Puits Baba May 1913, Terres Blanches May 1913 (Victor Faroult); Ain
Sefra, May 1913 (W. R. and E. H.) ; Zuilla, June 1913 (V. Faroult) ; Sebdou,
June 1918 (P. Rotrou).
48. Timora albida Hmpsn.
Timora albida Hampson, Ann. Mag. Nat. Hist. (7) xv. p. 450 (1905) (Algeria).
This insect has been much confused with the previous one.
The series at Tring consists of 81 specimens from Ain Sefra, May 1913-1915
( W. R. and E. H. and V. Faroult) ; halfway between Ouargla and El Golea, March
1912 (Hartert and Hilgert) ; Guelt-es-Stel and Terres Blanches, May 1913
(V. Faroult) ; Hassi Dinar, El Alia, Guerrara, El Arich, Hassi Sidi Mahmund,
and Oued Nca, April 1914 (Hartert and Hilgert).
2 $$ Hammam-es-Salahin, April 1904 (Lord Walsingham), are in British
Museum.
49. Argyrospila dulcis Oberth.
Argyrospila dulcis Oberthiir, Etud. Lipid. Comp. fosc. xvi. p. 23. pi. xdi. ff. 4052, 4053 (1919)
(Geryville).
I do not possess this species.
] 4 Novitates Zoolooicae XXVII. 1920.
50. Arenostola deserticola (Stdgr.).
Calamia deserticola Staudinger, Iris, vol. xii. p. 371. pi. 5. f. 10 (1900) (Biskra).
I have received a male and female of this species from Ain Sefra, June 1915
(V. Faroult) ; Environs de Batna, 1914 (A. Nelva).
The British Museum has 1 <$ Hammam-es-Salahin, April 1904, Lord
Walsingham.
51. Arenostola mabillei (D. Lucas).
Tapinostola mahillei Daniel Lucas, Bull. Soc. Entom. France, 1907, p. 342 (Le Tarf).
I have 1 $ Foret de Tenira, November 1918 (P. Rotrou).
52. Oria fulva africana (Oberth.).
Tapinostola fulva africana Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 26. pi. xdi. ff. 4048^050
(1919) (Geryville, Aflou).
The Tring series, all $$, consists of 9 specimens from Sidi-bel- Abbes, September
—October 1917 (M. Rotrou) ; Foret de Tenira, October 1918 (P. Rotrou).
53. Archanara neurica (Hiibn.).
Noctua neurica Hiibner, Europ. Schmett. Xoct. f. 381 (1808).
I have not received this from Mauretania.
54. Archanara dissoluta (Hiibn.).
Noctua dissoluta Hiibner, Europ. SchmetCNoct. ft. 659-661 (1818).
I have 3 Algerian examples : 1 (J Hammam R'hira, May 1913 (W. R. and
E. H.) ; 1 ? Hammam Meskoutine, May 1914 (W. R. and E. H.) ; 1 <J Sidi-bel-
Abbes, July 1916 (M. Rotrou). The Hammam R'hira <J is quite black, as is the
Sidi-bel-Abbes one.
55. Archanara affinis sp. nov.
This species is very close to neurica, but is darker, more blackish and can be
at once distinguished by the 4 black points at the 4 corners of the reniform and
the black points below the orbicular. This is possibly what Mr. Oberthiir calls
neurica.
1 (J Sidi-bel-Abbes, June 1917 (M. Rotrou).
56. Stilbia anomala calberlae (Faill.).
Caradrina calberlae Failla-Tedaldi, Nat. Sicil. vol. x. p. 29. pi. 1. f. 4 (1890) (Sicily).
• 3 (JcJ, 1 ? El Mahouna, September 1919 (V. Faroult).
57. Stilbia algirica Culot.
Stilbia algirica Culot, Nod. et Geom. d'Eur. pt. i. vol. ii. p. 45. pi. 45. f. 18 (1914) (Geryville).
We only received this very distinct species from Guelt-es-Stel and Aflou ;
44 specimens Guelt-es-Stel October 1912, Aflou October 1916 (V. Faroult) are
at Tring.
1 <J, 1 $ Guelt-es-Stel (ex Tring Museum) are in the British Museum.
Novitates Zoolooicae XXVII. 1920. 15
58. Stilbia turatii D. Lucas.
Stil'oia turatii Daniel Lucas, Bull. Soc. Entom. France, 1910, p. 272 (Le Tarf).
I have never received this species. Up to March 1919 the only known
specimens number 8, all $$, viz. 2 from Le Tarf hi coll. Daniel Lucas, and 4 Ain
Draham, 1 Maafa and 1 Amasia, all in coll. Oberthiir.
59. Stilbina numida (Oberth.).
Hypeuthina numida Oberthiir, Etud. Entom. Fase. xiii. p. 27. pi. 6. f. 41 (1890) (.Magenta).
We have principally received this species from Guelt-es-Stel.
There are at Tring 110 S3, 18 $$ Guelt-es-Stel October 1912-1913, 2 $$,
2 $0 Perregaux October 1915 (V. Faroult) ; 1 $ Sidi-bel-Abbes, November 1917
(M. Rotrou) ; 1 ? Batna (A. Nelva).
In the British Museum are 3 <$<$ ex Tring Museum.
60. Brithys pancratii (Cyr.).
Noctua pancratii Cyrillo, Entom. Nap. pi. 12. f. 4 (1787) (Naples).
The Tring series consists of 32 specimens from Environs d' Alger (Captain
Holl and Dr. Nissen) ; Ain Draham, July 1911 (V. Faroult) ; Belvedere, Tunis,
August— September 1915 (M. Blanc) ; Environs de Setif, 1911 (V. Faroult).
61. Brithys encausta (Hubn.).
Noctua encausta Hiibner, Samml. Europ. Schmett. Noct. f. 392 (1827).
1 have received 4 specimens of this species from Mauretania.
2 S6, -' 9? Tunis.
62. Spodoptera abyssinia Guen.
Spodoptera abyssinia Guenee, Hist. Nat. Ins. Spec. Gen. Lipid, vol. v. Noct. vol. i. p. 154 (1852)
(Abyssinia).
Mr. Oberthiir has used Lederer"s name for this insect because Guenee remarks
on the label of a specimen " not compared with type," and moreover put it in the
genus Caradrina = recte Athelis, where it does not belong. Now because an
author remarks he has not compared his specimens with his own type in another
collection, it is no reason to say he doubted the identification, and we thus see
into what nomenclatorial muddles those writers can bring us who strictly adhere
to the shibboleth that a good figure alone makes a name valid.
The Tring Museum has 29 Mauretanian examples from Biskra, March —
April 1908-1909 (W. R. and E. H.) ; Mazagan, Morocco, October — December
1902 (W. Riggenbach) ; Rabat, Morocco, August 1913 (A. Thery).
63. Athetis germaini (Dup.).
BryophiUi germaini Duponchel, Ann. Soc. Entom. France, vol. iv. p. 194. pi. 4a. f. 2 (1835) (Mont-
pellier).
Although Mr. Oberthiir says this is extremely common in Algeria, strange
to say I only have received 2 specimens.
1(J,1? Guelt-es-Stel, October 1912 and September 1913 (V. Faroult).
16 Xovitates ZooLooroAE XXVII. 1920.
64. Athetis aspersa (Ramb.).
Caradrina aspersa Rambtir, Ann. Soc. Entom. France, vol. iii. p. 385. pi. 8. f. 3 (1834) (.Marseilles).
I have not received this insect.
65. Athetis atriluna (Guen.).
Caradrina atriluna Guenee, Hist. Nat. Ins. Spec. Gin. Lipid, vol. 5. Noct. vol. i. p. 252 (1852)
(Abyssinia).
This insect is not recorded by Mr. Oberthiir.
The Tring series consists of 8 JcJ, 10 $$ from Mazagan August 1901 , Seksawa
April 1905, Morocco (W. Riggenbach) ; Perregaux, September 1915 (V. Faroult) ;
Sidi-bel-Abbes, September 1917 (M. Rotrou).
66. Athetis alsines (Brahm).
Noctua alsines Brahm, Ins. Kal. vol. ii. p. 114 (1791) (Mayence).
This species also is not mentioned by Oberthiir.
1 ? Am Draham September 1911, 1 $ Guelt-es-Stel October 1913 (V.
Faroult).
67. Athetis blanda (Schiff. and Den.).
Noctua blanda ScliirTermuller and Denis, Ank. Sysl. Werk. Schmelt. Wienergeg. p. 77 (1775) (Vienna).
This is also not recorded by Mr. Oberthiir. Mr. Culot figures it on pi. 48,
f. 4 of his Noctuelles et Geometres d' Europe, under the name of laraxaci Hiibn.,
which however dates from 1818 only.
The Tring series consists of 14 <Jc?> 35 $$ Am Draham, August — September
1911 (V. Faroult).
68. Athetis casearia (Stdgr.).
Caradrina casearia Staudinger, Iris, vol. xii. p. 375. pi. 5. f. 1 (1899) (Jordan Valley).
I have not received typical casearia or the ab. bilineata Culot.
69. Athetis pertinax inumbrata (Stdgr.).
Agrotis inumbrata Staudinger, Iris, vol. xii. p. 363 (1899) (Zeitun).
Victor Faroult sent me 2 <JrJ of this fine insect, hitherto only known from
Asia Minor. 2 $$ Perregaux, October 1915 (V. Faroult).
70. Lycophotia kermesina (Mab.). (PI. XVII. f. 19.)
Noctva kermesina Mabille, Ann. Soc. Entom. France (4) 9. p. 55. pi. 2. fig. 10 (18G9) (Boscognagno,
Corsica).
Mr. Oberthiir has described Caradrina sua vis and Mr. Culot Caradrina
flavida ; and Mr. Oberthiir suggests that these two insects may possibly be only
colour varieties of kermesina Mabille. This is certainly the fact, and as kermesina
is extremely variable, Mr. Oberthur's subspecific name of dclectans must also
sink.
NOV1TATES ZOOLOQICAE XXVII. 1920. 17
The series at Tring consists of 92 specimens from Environs de Batna, 1913—
1914 (Nelva coll.) ; Aflou, September 1916 (V. Faroult) ; Guelt-es-Stel, Sep-
tember—November 1912-1913 (V. Faroult).
71. Athetis astigmata Rothsch.
Athelis astigmata Rothschild, Novit. Zool. vol. xxi. p. 336. No. 193 (1914) (Guelt-es-Stel).
As I had not figured this species, Mr. Oberthiir as usual calmly ignored it,
and redescribed it as devitifimbriata in his Fasc. XVI. p. 58 (1919).
I have 1 (J, 2 $$ Gueltes-Stel, October— November 1913 (V. Faroult).
72. Athetis ambigua (Schiff. and Den.).
Noclua ambigua Schiffermiiller and Den. Ank. Syst. Werk. Schmett. Wienergeg. p. 77 (1775) (Vienna).
The Mauretanian series at Tring consists of 197 specimens from Guelt-es-Stel,
May 1913 (V. Faroult) ; Environs de Batna, 1909-1912 (Nelva coll.) ; Lambessa,
October 1915 (Nelva coll.) ; Hammam Meskoutine, April — May 1914 (W. R.,
K. J., and E. H.) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Sebdou, May
1918 (P. Rotrou) ; Perregaux, October 1915 (V. Faroult) ; Khenchela, May 1912
(W. R. and K. J.) ; Hammam R"hira, May— June 1911-1915 (W. R., E. H., and
Faroult) ; Oued Hamidou, June 1914 (V. Faroult) ; Bou Cedraia, May 1913 (V.
Faroult) ; Ain Draham, September 1911 (V. Faroult) ; Imitaut and Mazagan,
Morocco, May 1902-1904 (W. Riggenbach) ; Environs dAlger, May— September
1908 (W. R., K. J., and Dr. Nissen) ; El Mahouna, September 1919 (V. Faroult).
73. Athetis kadenii rufostigmata Rothsch.
Athetis rufostigmata Rothschild, Novit. Zool. vol. xxi. p. 335 (1914) (Guelt-es-Stel).
Mr. Oberthiir says that the Algerian form is proximo, Rambur, but I consider
it to be distinct, as it has the reniform stigma much darker, rufous not orange-
yellow, and more strongly marked.
I am convinced also that kadenii is a distinct species, not a form of fusci-
cornis Ramb., as Sir George Hampson has stated it to be.
We have at Tring 48 specimens from Guelt-es-Stel, October 1913 (V.
Faroult); Sidi-bel-Abbes, September 1917 (M. Rotrou); Saida, May 1913
(W. R. and E. H.) ; Perregaux, October 1915 and Masser Mines, June 1914 (V.
Faroult) ; Environs de Batna, 1909-1912 (Nelva and V. Faroult) ; Khenchela,
May 1912 (W. R. and K. J.) ; Hammam R'hira, May 1913 (W. R. and E. H.) ;
Oued Hamidou June 1912, and Bordj-ben-Aneridj October 1912 (V. Faroult) ;
Les Pins, September 1918 (M. Rotrou) : Sebdou June, Foret deTenira September
1918 (P. Rotrou).
74. Athetis hispanica (Mab.).
Caradrina hispanica Mabille, Ann. Soc. Entom. France, vol. lxxv. p. 30. pi. 3. f. 1 (1906) (La Granja).
Mr. Oberthiir places this as a local race of -selini Boisd., while Sir George
Hampson considers it a distinct species. If Mr. Culot's figures of selini are
correct, it is abundantly distinct.
I have 9 specimens from Batna (Nelva coll.) ; Biskra, March 1914 (W. R.
and E. H.); Souk Ahras, April 1914 (W. R. and K. J.); Sidi-bel-Abbes,
September 1917 (M. Rotrou).
18 NOVITATES ZOOLOGICAE XXVI I. 1920.
75. Athetis ingrata (Stdgr.).
Caradrina ingrata Staudinger, Iris, vol. x. pp. 175, 286. pi. 4. f. 13 (1S97) (Syria).
I have only received 1 specimen of this species, which appears to be very
rare in Mauretania.
1 cJ Environs de Batna, 1911-1912 (Nelva coll.).
76. Athetis flavirena (Guen.).
Caradrina flanrena Guenee, Hist. Nat. Ins. Spec. Gen. Lipid, vol. v. Noct. vol. i. p. 250 (1852).
The Tring series from Mauretania consists of 15 <$<$, 19 $$ from Blida les
Glacieres, June 1908 (W. R. and K. J.); Guelt-es-Stel, October 1912 (V.
Faroult) ; Foret de Tenira, September 1918 (P. Rotrou) ; Environs d' Alger
(Captain Holl) ; Environs de Batna (Nelva coll.) ; Berrouaghia, April 1914 (V
Faroult) ; Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and V.
Faroult).
77. Athetis flava (Oberth.).
Caradrina flava Oberthiir, Etud. Entom. fasc. i. p. 45. pi. 4. t. 3 (1876) (Algeria).
Mr. Oberthiir states that this insect varies much in size, but I have not
found this to be the case. The small specimens that I have received all belong
to my approximans, which is conspicuous by the heavy and broad greyish termen.
The Mauretanian series at Tring consists of 204 specimens from Biskra,
April 1908— March 1914 (W. R. and E. H.) ; Bordj Mecht-el-Kaid, April 1909
(W. R. andE. H.) ; Bou Saada, April 1911— March 1912 (V. Faroult) ; Tilghemt
April 1912 (V. Faroult) ; Ghardaia, April 1911 (W. R. and E. H.) ; El Kantarn
March— April 1911 (Faroult); Khenchela, June 1911 (V. Faroult); South
Oued Mya and North of Am Guettera, April 1912 (Hartert and Hilgert) ;
Environs de Setif, 1911 (Faroult) ; Berrouaghia, April 1914 (V. Faroult) ; En-
virons de Batna, 1913-1914 (Nelva coll.) ; Guelt-es-Stel, April 1913 ; Djebel
Autan May 1918, Bordj Chegga March 1917, A'in Sefra March 1915,
Mecheria May 1918 (V. Faroult) ; Souk Ahras, April 1914 (W. R. and K. J.) ;
Oued Nca, April 1914 (Hartert and Hilgert) ; Oud Dehin and Oued Ag-eld,
Timenaiin, March 1914 (Geyr von Schweppenburg).
The British Museum has 1 (J Algeria, Mrs. Nicholl ; 2 tftf El Kantara, April
1913, P. A. Buxton.
78. Athetis oberthuri Rothsch. (PI. XVII. f. 26.)
Athetis oberthuri Rothschild, Novit. Zool. vol. xx. p. 126. No. 57 (1913) (South Oued Mya).
The Tring Museum possesses 1 cj, 1 $ Oued Nca, April 1914, 1 <J, 3 $° from
South Oued Mya, April 1912 (Hartert and Hilgert).
This species is very similar to casearia Stdgr., but much more heavily marked.
79. Athetis approximans Rothsch.
Athetis approximans Rothschild, Novit. Zool. vol. xxi. p. 334. No. 1S7 (1914) (Guelt-es-Stel).
The Tring series consists of 131 specimens from Rharis, April 1914 (Geyr von
Schweppenburg) ; Guelt-es-Stel, August — October, 1912-1913 (V. Faroult) ; Les
NOV1TATES ZOOLOGICAE XXVII. 1920. 19
Pins, September 1918 (M. Rotrou) ; Ain Sefra April 1915, Metliti September
1917 (V. Faroult) ; El Mahouna, September 1919 (V. Faroult).
Mr. Oberthiir has treated this as a dwarf form of flava, but besides the
differences in marking, Sir George Hampson, who has carefully examined speci-
mens, tells me it belongs to a different section of the genus.
The British Museum has 1 (J Guelt-es-Stel ex Tring Museum.
80. Athetis scotoptera (Ptingl.).
Caradrina scotoptera Pungler, Iris, vol. xxviii. p. 47. No. 19. pi. iii. f. 18 (1914) (Jerusalem).
This species is not recorded by Mr. Oberthiir.
We have at Tring 2 $<$, 3 $$ from Environs de Batna (Nelva coll.) ; Foret
de Tenira, October 1918 (P. Rotrou) ; Sidi-bel-Abbes, September 1917 (M.
Rotrou).
81. Athetis jacobsi Rothsch.
Athetis jacobsi Rothschild, Novit. Zool. vol. xxi. p. 335. No. 190 (1914) (Guelt-es-Stel).
The series at Tring consists of 288 specimens from Guelt-es-Stel, September —
October 1912-1913 (V. Faroult); Foret de Tenira, October 1918 (P. Rotrou);
Environs de Batna (Nelva coll.) ; Metlili, September 1917 (V. Faroult) ; El
Mahouna, September 1919 (V. Faroult).
82. Athetis clavipalpis (Scop.).
Phalaena clavipalpis Scopoli, Entom. Car. p. 213 (1763) (Carniola).
Mr. Oberthiir quotes this under Schiffermuller's name, because Guenee did
so, but both Fabricius' name of quadri punctata and clavipalpis of Scopoli are older.
In my account of the Lepidoptera of Guelt-es-Stel in 1914 I was misled
by Mr. Warren's account of this insect in Seitz, and kept the small specimens
apart as a distinct species under the name grisea, but they are only dwarf indi-
viduals of clavipalpis, and if distinguished at all must stand as ab. minor. As
grisea Rott. is only a synonym of clavipalpis and dates from 1776, grisea Eversm.
1 848 must stand as cinerascens Tengstr.
The Tring series from Mauretania consists of 677 specimens from Biskra,
March 1908— April 1914 (W. R. and E. H.) ; Hammam R'hira, May 1908— May
1913 (W. R., E. H., and K. J.) ; Blida les Glacieres, June 1908 (W. R. and K. J.) ;
Environs d' Alger, June 1908 (Dr. Nissen) ; Djebel Cheddar, Mazagan, April 1902,
and Seksawa, April — May 1905, Morocco (W. Riggenbach) ; Guelt-es-Stel, April
—October 1912-1913 (W. R. and K. J., and V. Faroult) ; Sidi-bel-Abbes, June-
October 1917 (M. Rotrou) ; Perregaux, October 1915 (V. Faroult) ; Ain Sefra,
May 1915 (V. Faroult) ; Lalla Marnia, May— October, 1914 (V. Faroult) ; Masser
Mines, May 1914 (V. Faroult) ; Hammam Meskoutine, April — May 1914 (W. R.,
E. H., and K. J.) ; Environs de Batna (Nelva coll.) ; Ain Draham, September
1911 (V.Faroult) ; Bou Saada and Tilghemt, April 1912 (V. Faroult) ; Khenchela,
May 1912 (W. R. and K. J.) ; Sebdou June, Sidi Djilali September, Foret de
Tenira August 1918 (P. Rotrou) ; El Mahouna, September 1919 (V. Faroult).
In British Museum, 1 <$ El Kantara, April 1913, P. A. Buxton.
20 Novitates Zoological XXVII. 1920
83. Laphyma exigua (Hiibn.).
Noctua exigua Hiibner, Europ. Schmett. Noct. f. 3G2 (1808).
Of this very cosmopolitan insect the Mauretanian series at Tring consists of
477 specimens from Guelt-es-Stel, April — November 1912-1913 (V. Faroult) ;
El Kantara, June 1909 (Sidi Brahim) ; Environs d' Alger, May 1906-1908 (W. R.,
K. J., and E. H., and Dr. Nissen) ; Seksawa April 1905, Mazagan June 1900 —
May 1902, Rahama, S.E. of Mazagan, May 1903 (W. Riggenbach) ; Hammam
R'hira, May 1908— June 1916 (W. R., E. H., and K. J., and Faroult) ; Colomb
Bechar, February 1912 (V. Faroult) ; Laghouat March, Tilghemt April 1912,
Bou Saada April— May 1911-1912 (V. Faroult) : Ghardaia, April 1911 (W. R.
and E. H.) ; North of El Golea, South Oued Mya, Ain Guettera, and In Salah and
Igosten Tidikelt Oases, March — April 1912 (Hartert and Hilgert) ; Khenchela,
May 1912 (W. R. and K. J.) ; Blida, December 1915 (Faroult) ; Oued Nca and
Sands of El Arich, June 1912 (Hartert and Hilgert) ; Environs de Setif, 1911 (V.
Faroult) ; Oued Hamidou, June 1912 (V. Faroult) ; Sidi-bel-Abbes, June —
August 1917 (M. Rotrou) ; Biskra, April 1908-1914 (W. R. and E. H.) ; Masser
Mines, June 1914 (V. Faroult) ; Perregaux, October 1915 (Faroult) ; Ain Sefra,
April 1913— July 1915 (W. R. and E. H., and Faroult); Lalla Marnia and
Moroccan Frontier, April — May 1914 (Faroult) ; Temassinin, Amgid, Oued Gif
Aman, Oued Dehin, and El Mesrane, Hoggar Country, November 1913 — March
1914 (Geyr von Schweppenburg) ; Sidi Ferruch, November 1911 (Thery) ;
Environs de Batna, 1911-1914 (Nelva coll.) ; Hammam Meskoutine, April — May
1914 (W. R., E. H., and K. J.) ; Ain Draham, September 1911 (V. Faroult) ;
Oued Abbou, Timassiuin, I-n-Kelemet, 30 kil. N. of Amgid, Amgid, Temenaiin,
Oued Ag'elil, Oued Dehin, Oued Gif Amdu, January — March 1914 (Geyr von
Schweppenburg) ; El Mahouna, June 1919 (V. Faroult).
The British Museum has 1 $ El Kantara, April 1913, P. A. Buxton.
84. Prodenia litura (Fabr.).
Noctua litura Fabrioius, Syst. Entom. p. 601 (1775) (East Indies).
Of this widespread species I have from Algeria 1 64 specimens, from Perre-
gaux, September — October 1915 ; El Kantara, El Outaya, August 1917 (V.
Faroult) ; Biskra, March— June 1908-1912 (Hartert and Hilgert, W. R., and
Faroult); Sidi-bel-Abbes, August — September 1917 (M. Rotrou).
Mr. Oberthur employs Herrich-Schaffer's name retina for this species
because he first figured it.
85. Ulochlaena hirta (Hiibn.).
Noctiia hirta Hiibner, Europ, Schmett. Noct. f. 591 (1827).
Of this species I have only received 1 $ from Mauretania, all the rest are $$.
The Tring series numbers 196 Algerian specimens from Environs de Batna (Nelva,
Faroult, and Staudinger) ; Bordj-ben-Aneridj, October 1912 (V. Faroult) ; Aflou,
October 1916 (V. Faroult) ; 1 $ Hammam R'hira, March 1916 (V. Faroult). -
The $ is flightless.
NOVITATES ZOOLOOICAE XXVII. 1920. 21
86. Derthisa trimacula (Schiff. & Den.).
Bombyx trimacula Schiffermuller and Den. Ant. Syst. Werk. Schmett. Wienergeg. p. 59 (1775) (Vienna).
This is one of the most variable of known heterocera, and a number of indi-
vidual forms have received names, among them ab. hisjxtna Boisd. grey with sharp
dark pattern, ab. dentimacula Hiibn. same colour but dark marking reduced, ab.
glavcina Esp. uniform rufous, ab. tcrsa Schiff. yellow dark marks in cell only, ab.
gruneri Boisd. == albida Oberth. same only white, ab. tersina Stdgr. same only
grey, ab. unicolor Dup. entirely yellow or buff.
We have at Tring from Mauretania 1,191 specimens from Guelt-es-Stel,
September— November 1912-1913 (V. Faroult) ; Batna (Nelva coll., Staud.
and Faroult) ; Bordj-ben-Aneridj, October 1912 (V. Faroult) ; Environs de
Setif, 1911 (V. Faroult); Lambiridi, October 1910 (V. Faroult); Perregaux,
October 1915 (V. Faroult); Afiou, September 1916 (V. Faroult); Foret de
Tenira, October 1918 (P. Rotrou) ; Sidi-bel-Abbes, October 1917 (M. Rotrou).
In the British Museum are 1 <$, 1 $ Batna, Staudinger and Bang-
Haas (ab. albida).
87. Grammoscelis magnifica (Rothsch.).
Derthisa magnified Rothschild, Novil. Zool. vol. xxi. p. 328. No. 145 (1914) (Guelt-es-Stel).
Sir George Hampson pointed out to me that although this fine insect was
a true Cucullid, it was not, as I thought, a Derthisa but a Grammoscelis.
The series at Tring consists of 67 S3, 25 $$ from Guelt-es-Stel, October —
November 1913 (V. Faroult) ; El Mesrane, November 1913 (V. Faroult) ;
Perregaux, November 1915 (V. Faroult); Bordj-ben-Aneridj October 1912,
Medjez October 1911 (V. Faroult).
88. Aglossestra mariae-ludovicae (D. Lucas).
Hadula mariae-ludovicae Daniel Lucas, Bull. Soc. Entom. France, 1914, p. 311 (Tunis).
Derthisa a/finis Rothschild, Novit. Zool. vol. xxi. p. 328. No. 146 (1914) (Guelt-es-Stel).
My description appeared in October, while that of Monsieur Daniel Lucas
was published in June, so his name has priority.
This species belongs to the genus Aglossestra of the subfamily Hadeninae.
1 (J GuehVes-Stel, October 1913 (V. Faroult).
The Genus Heliophobus Boisd.
Mr. Oberthiir, following Guenee, makes use of the genus Heliophobus Boisd.
and puts into it hispida Hiibn. ; scillae Chret. ; pierretii Oberth. (nee Bugnion) ;
messaouda Oberth. ; and orana Oberth. (nee Lucas) : a regular olla podrida.
• Neither Mr. Oberthiir nor the other authors who have used Heliophobus
should have done so, as Boisduval himself states (Europ. Lepid. Ind. Meth. 1829,
p. 69) that it is another name for Hadena Treitschke.
Of the 5 species put in it by Mr. Oberthiir, hispida Hiibn. and scillae Chret.
belong to the genus Leucochlaena of the subfamily Cuculliinae ; messaouda Oberth.
and orana Oberth. (nee Lucas) belong to the genus Euxoa of the subfamily
Agrotinae ; and pierreti Oberth. (nee Bugnion) belongs to the genus Pseudo-
pseuslis of the subfamily Zenobiinae ( = Acronyctinae).
" N0V1TATES ZOOLOGICAE XXVII. 1920.
89. Leucochlaena oditis (Hiibn.).
Noctua oditis Hiibner, Europ. Schmett. Xoct. ff. 694. 695 (1822).
There appear to be two forms of this species in Algeria, a small paler form,
and a large dark form, but they do not seem locally constant and intergradations
occur.
The series at Tring consists of 151 specimens from Guelt-es-Stel, Sep-
tember—November 1912-1913 (V. Faroult) ; Aflou, September 1916 (V. Faroult) ;
Foret de Tenira, October 1918 (P. Rotrou) ; Ain Draham, September 1911 (V.
Faroult) ; Batna (Nelva coll.) ; El Mesrane, November 1913 (V. Faroult) ; Sidi-
bel-Abbes, October 1917 (M. Rotrou) ; El Mahouna, September 1919 (V.
Faroult).
90. Leucochlaena scillae (Chret.).
Heliopho'jtts scillae Chretien, Le Naluraliste, vol. x. p. 92 (1888) (Bone).
26 (S3 El Mahouna, September 1919 (V. Faroult).
I have only 1$ specimen of the ab. datini Oberth.
1 <J Ain Draham, October 1911 (V. Faroult).
In the British Museum there is 1 $ Bone, Abbe de Joannis.
[Euxoa pierretii (Bugnion).
Episema pierretii Bugnion, Ann. Soc. Entom. France, 1837. p. 441. pi. 16. f. 3 (Egypt).
Heliophobu-s marsdeni Bethune Baker, Trans. Entom. Soc. Lond. 1894. p. 40. pi. i. f. 9 (Egypt).
This and the next species form a striking example of the fallacy of Mr.
Oberthiir's dictum " Pas de bonne figure, pas de nom valable," for Monsieur
Bugnion gives an excellent figure of the insect afterwards described by Bethune
Baker as marsdeni and which is an Agrotid of the genus Euxoa, and yet both Mr.
Oberthiir and Mr. Culot describe and figure as pierretii Bugnion a totally different
insect afterwards described as Taeniocampa iellieri by Daniel Lucas, and which
belongs to the subfamily Zenobiinae. Euxoa pierretii, as far as I can discover,
has not yet been taken in Mauretania.]
91. Pseudopseustris tellieri (D. Lucas).
Taeniocampa tellieri Daniel Lucas, Bull. Soc. Entom. France, 1907, p. 196 (Gafsa).
Heliopho'nts pierretii Culot (nee Bugnion), Noct. el Geom. d'Eur, pt. i. vol. i. p. 174. pi. 32. f. 6 (1913)
(Biskra).
Harpagoplmna diacrisioides Rothschild, Novit. Zool. vol. xxi. p. 326. No. 130 (1914) (Guelt-es-Stel).
This is the insect identified by Messieurs Oberthiir and Culot as Euxoa
pierretii (Bugnion), but Mr. Culot has gone further and figured the same insect
twice, once under the name of pierretii, and once under its true name of tellieri.
Then unfortunately I also made a stupid error of negligence and redescribed it
once again.
The Tring Museum possesses 3 specimens : 1 rj, 1 $ Guelt-es-Stel, October
1912-1913 (V. Faroult) ; 1 <J El Mesrane, November 1913 (V. Faroult).
In the British Museum there is 1 <J Batna, Staudinger and Bang-Haas.
NOVITATES ZOOLOQICAE XXVII. 1020. 23
92. Leucochlaena orana (Lucas). (PI. XV. £f. 27, 28.)
Episema orana Lucas, Expl. Scient. d'Algirie, pt. iii. p. 384. pi. 3. i. 7 (1849) (West Algeria).
Here again is shown the fallacy of insisting that figures are everything.
Messrs. Oberthur and C'ulot have figured and described under the name of Helio-
■phobus orana (Lucas) an insect which is not only not orana but belongs to a very
different subfamily ; and yet Lucas gives a recognisable figure.
The series at Tring contains 7 <$,$, 3 §§. 1 3 Oudjda, Morocco November
1914, 1(J LallaMarnia December 1914, 1 ^LaMacta September 1915, 4 $$, 3$$
Perregaux October 1915 (Victor Faroult).
93. Euxoa noctambulatrix (Chret.). (pi. XV. f. 20.)
Gladocerotis noctambulatrix Chretien, Ann. Soc. Entom. France, p. 502 (1910) (Gafsa).
Cladocera orana Oberth. (nee Lucas), Etiul. Lipid. Cornp. fasc. vi. p. 332, pi. exxviii. f. 1139 (1912)
(Geryville).
This insect, which both Oberthur and Culot figure as orana, is an Agrotid and
not a Cucnllid, as the true orana is. Among minor differences the $ has abortive
wings, while the $ of true orana is full winged, like the <$. It is curious that at
the same time as Mr. Oberthur declares his orana to be an aberration of Chretien's
noctambulatrix he figures them under the two names, and actually puts them in
two different genera, Cladocerotis and Cladocera ! ! !
I quote this insect temporarily under Chretien's name noctambulatrix, because
I have not been able to compare my specimen with Spanish ones, of which none
are in England ; I feel sure, however, that when they can be compared they will
prove that this insect is the same as Heliophobus boetica Boisd. Should this
prove the case, the species would have to stand as Euxoa boetica Boisd.
1 (J Sidi Ferruch (Thery coll.) ; 1 <S Sebdou, September 1908 (P. Rotrou).
94. Euxoa messaouda messaouda (Oberth.).
Luperina messaouda Oberthur, Etud. d' Entom. livr. ix. p. 39. pi. iii. f. 3 (1884) (Sebdou).
This species was abundant at Guelt-es-Stel.
The series at Tring consists of 518 specimens from Guelt-es-Stel, October —
November 1912-1913 (Victor Faroult); Aflou, September— October 1916 (V.
Faroult) ; Mazagan, Morocco, September 1903 (W. Riggenbach).
Among the Guelt-es-Stel series are several^ $ in which the red is quite absent :
these agree absolutely with the Spanish form messaouda matritensis Vasq. This
demonstrates the fact that an insect can occur sporadically among the typical
form as an aberration, and yet in another locality assume the status of a distinct
subspecies.
95. Omphaloscelis polybela (de Joan.).
Euxoa polyhela de Joannis, Bull. Soc. Entom. France, 1903. p. 28 (Philippeville).
The Tring Museum possesses 306 specimens from Environs de Batna, Sep-
tember—October 1910-1915 (Nelva, V. Faroult, Staudinger) ; Bordj-ben-Aneridj ,
October 1912 (V. Faroult); Sidi-bel-Abbes, November 1917 (M. Rotrou);
Foret de Tenira, October 1918 (P. Rotrou).
In the British Museum are 1 (J, 1 $ Batna, Staudinger and Bang-Haas.
24 Novitates Zoolooicae XXVII. 1920.
96. Cladocerotis optabilis 'Boisd.).
Heliophobus optabilis Boisduval, Icon. Lepid. Eur. vol. ii. pi. 74. IT. 2, 3 (1832).
The ground-colour and the markings vary considerably, the latter being
sometimes lemon-yellow, sometimes grey, and sometimes almost pure white ;
all the specimens I have seen from Sicily are like the last named, but I have a
number from Algeria quite identical.
We have at Tring 308 specimens from Environs de Batna, September —
October, 1910-1915 (Nelva. V. Faroult. and Staudinger) ; Sidi-bel- Abbes, Sep-
tember—October 1917 (M. Rotrou) ; Foret de Tenira, October 1918 (P. Rotrou) ;
Perregaux, October 1915 (V. Faroult); Lalla Marnia, November 1914 (V.
Faroult) ; Guelt-es-Stel October— November 1912-1913, Aflou October 1916
(V. Faroult).
The genus Cladocera Rmb. is preoccupied, so Sir George Hampson made the
genus Clndocerotis for this species.
In the British Museum are 3 <$£, 1 $ Guelt-es-Stel ex Tring Museum.
97. Euxoa rugifrons (Mab.).
Agrotis rugifrons Mftbille, Bull. Soc. Entom. France, 1SSS. p. 42 (Gabes).
Agrotis bledi Chretien, Ann. Soc. Entom. France, 1910, p. 500 (Gafsa).
Agrotis urbana Bang-Haas, Iris, vol. xxv. p. 142. pi. vi. tig. 7 (1912) (Batna).
This species is very common in Algeria. Our series at Tring consists of 504
6pecimens from Guelt-es-Stel, October — November 1912-1913 (V. Faroult);
Aflou, September — October 1916 (V. Faroult) ; Environs de Batna, September —
October 1909-1914 (Nelva coll.) ; Bordj-ben-Aneridj, October 1912 (V. Faroult) ;
Medjez October 1911, Aflou October 1916 (V. Faroult).
Neither Mr. Oberthiir nor Mr. Culot mention the name rugifrons Mab.
98. Euxoa capsensis Chret.
Euxoa capsensis Chretien. Ann. Soc. Entom. France, 1910, p. 497 (Gafsa).
Euxoa muriicolor Rothschild, Novit. Zool. vol. xxi. p. 319. Xo. S3 (1914).
I have only received this species from Guelt-es-Stel.
80 Guelt-es-Stel, October 1912-1913 (V. Faroult).
99. Euxoa lasserrei (Oberth.).
Lvperina lasserrei Oberthiir, Etud. d" Entom. Fasc. vi. p. 86. pi. xi. ff. 13, 14 (18S1) (ilagenta, Sebdou).
The Tring series contains 240 specimens from Guelt-es-Stel, October —
November 1912-1913 (V. Faroult); Les Pins, September 1918 (M. Rotrou) :
Foret de Tenira, October 1918 (P. Rotrou) ; Batna, November 1910-1911 (V.
Faroult and Nelva); El Mesrane November 1912, Aflou September 1916, Aflou
October 1916 (V. Faroult) ; Tunis (Max Bartel).
The British Museum has 1 £ Mauretania.
100. Euxoa obesa lipara (Rambur).
Agrotis lipara Rambur, Ann. Soc. Entom. France, 1S48, p. 68 (Algeria).
Sir George Hampson places lipara, without comment, as a synonym of obesa,
while Mr. Oberthiir treats it as a distinct species. The truth, however, lies in
between, for lipara is a southern form of obesa and must be treated as a subspecies.
NOVITATES ZOOLOGIOAE XXVII. 1920. 25
Our Tring series totals 497 specimens from Guelt-es-Stel, September — October,
1912-1913 (V. Faroult) ; Environs de Batna, Lambessa, September, October
1 909-1 914 (Nelva, Staudinger) ; Sebdou, September 1918 (P. Rotrou) ; Tlemcen,
1915 (P. Rotrou) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Aflou, October
1916 (V. Faroult).
101. Euxoa crassa (Hiibn.).
Noctua crassa Hiibner, Samml. Eur. Schmett. S. 151, 152, 560 (1881).
Treitschke (Schmett. Eur. vol. v. pt. i. p. 166. No. 19) gives a long explanation
of how the erroneous identification of the present species with tritici Linn, arose
and complains that Hiibner made matters worse by giving three figures of
crassa and calling f. 1 51 tritici Linn. Sir George Hampson has caused still further
difficulty by quoting crassa as of Treitschke, while its author was Hiibner, which
is evident from Treitschke's own quotations. Sir George omits the ff. 151 and 152
altogether.
Sir George Hampson, Mr. Oberthiir, Mr. Culot, and most of the authors since
Treitschke have united specifically crassa Hiibn. and lata Treit., in some cases
because they thought they were representative forms, in others because they con-
sidered them simply aberrations. Mr. Culot has committed a further error,
influenced by Mr. Oberthiir' s statements : he figures as var. golickei Ersch. a
Castille specimen lent by Mr. Oberthiir.
E. golickei was described from Turkestan, and has the heavily plumed
antennae characteristic of lata, of which it is undoubtedly a subspecies.
Moreover, lata never occurs on the mainland of Europe, so Mr. Oberthiir has
confounded a pale aberration of crassa with golickei, which latter is purely Asiatic.
Now, all the authors who have united crassa and lata have drawn
attention to two differences characteristic of lata ; one, the thicker and more
heavily pectinated antennae, holds good, but the second, the brighter and more
striking wing pattern, is not a constant character.
There are, however, three characters which specifically separate crassa and
lata quite definitely.
Firstly, the orbicular stigma in both series of lata has a distinct whitish
ring and stands out distinctly, while in crassa this ring is absent and the orbicular
appears almost obsolete.
Secondly, in $ crassa the hindwing is white shading into grey towards the
termen, and there is no trace of a discocellular stigma ; while in $ lata the hindwing
is brown, sometimes paler, or even whitish in the basal one-fourth, but always
with a distinct discocellular stigma, except in a very few extreme melanistic
individuals which are otherwise easily recognisable as lata.
Thirdly, thereof crassa have short pectinations to the antennae, and at the
distal end fully 4-5 mm. with no pectinations at all ; on the other hand, in lata
the antennae have long pectinations (in the projJortion of 16 to 9), and only the
last three or four joints are without pectinations.
Our Mauretanian series of crassa consists of 49 $3, ^0 9$ from Sidi-bel-Abbes,
September— October 1917 (M. Rotrou) ; Sebdou, September 1918 (P. Rotrou).
This species (crassa) appears entirely confined to West Algeria (Province
Oran), while lata occurs all over Algeria and portions of Tunis and Morocco.
26 Novitates Zoologicae XXVII. 1920.
101a. Euxoa lata (Treit.).
Agrotis lata Treitschke, Schmett. Eur. vol. x. pt. ii. p. 24 (1835) (Sicily).
This has since the time of Treitschke always been treated as a local race
or aberration of crassa, which is erroneous.
It is easily distinguished by the orbicular having a pale ring in both sexes,
in the antennae of the $ being much more strongly pectinated, and in the dark
hindwings with a discocellular stigma in the $.
The Tring series from Mauretania contains 63 <JcJ, 59 $$ from Environs
d' Alger (Dr. Nissen) ; Mazagan, Morocco, September 1902 (W. Riggenbach) ;
Rabat, Morocco (A. Thery) ; Messer September, Sidi-bel-Abbes September 1917
(M. Rotrou) ; Ai'n Draham, Tunisia October 1911, Perregaux October 1915 (V.
Faroult) ; Belvedere, Tunis, September 1915 (M. Blanc) ; Foret de Tenira,
September 1918 (P. Rotrou) ; El Mahouna, September 1919 (V. Faroult).
102. Euxoa vestigialis (Rott.).
Noctua vestigialis Rottemburg, Naturf. vol. viii. p. 107 (1776).
This appears to be unrecorded from Mauretania.
1 $ Lambessa, July 1914 (A. Nelva).
I have seen a second $ from Thala, Tunisia, taken by Mr. Daniel Lucas.
103. Euxoa spinifera (Hiibn.).
Noctua spinifera Hiibner, Samml. Eur. Schmett. Noct. f. 389 (1827).
Our Tring series contains 200 specimens from Guelt-es-Stel, May — November
1912-1913 (V. Faroult) ; Ain Draham, September 1911 (V. Faroult) ; Sidi-bel-
Abbes, July— September 1916-1917 (M. Rotrou) ; Foret de Tenira May, Sebdou
June 1918 (P. Rotrou) ; El Kantara, August 1917 (V. Faroult) ; Environs de Setif>
1911 (V. Faroult) ; Bou Saada March 1912, Laghouat March 1912 (V. Faroult) ;
El Ou Saya August 1918, Tilghemt April 1912 (V. Faroult) ; Biskra, March-
April 1908-1911 (W. R. andE. H.) ; Batna (Nelva and Faroult) ; Oued Hamidou,
June 1912 (V. Faroult) ; South Oued Mya April, Bordj Saada February 1912
(Hartert and Hilgert) ; Rabat, Morocco (A. Thery) ; Environs de Batna (A.
Nelva); Messer, September 1917 (M. Rotrou); Blida, November 1915 (V.
Faroult) ; Hammam R'hira, May —June 19C8-1916 (W. R. and K. J., and Faroult) ;
Mazagan February— May 1902-1903, Seksawa, Morocco April 1905 (W. Riggen-
bach) ; Environs d' Alger, May 1908 (W. R. and K. J.).
In the British Museum are 2 $$, 1 $ Hammam-es-Salahin, March 1904, Lord
Walsingham.
[Euxoa spinifera hodnae (Oberth.). (PI. XVII. ff. 15, 16.)
Agrotis hodnae Oberthiir, Etud. Entom. faac. iii. p. 45. pi. v. f. 8 (1878) (Bou Saada).
The large series of spinifera collected all over Algeria since 1878 have proved
that in Mauretania hodnae is only a sporadic aberration of spinifera, but in Egypt
it has developed into the local race and must stand as a subspecies as above.]
Novitates Zoolooicae XXVII. 1920. 27
104. Euxoa hoggari sp. nov. (PI. XVII. ff. 12-14.)
This is the insect erroneously named hodnae in 1915 (see Ann. Mag. Nat.
Hist. (8) xvi. p. 250. No. (16).).
cJ$. Ground-colour creamy white. Antennae brown with pale grey serra-
tions ; head and thorax whitish, more or less closely sprinkled with minute brown
streaks ; abdomen cream buff ; anal tuft buff.
Forewing cream- white, here and there streaked with pale wood brown, basal
one-sixth of costal area with dense dark brown markings, a brown wedge in cell,
reniform and spot below dark brown, a pale wood brown irregular band across
wing enclosing reniform, an oval stigma on vein 2 joined by a deeply zigzag
blackish line to inner margin, fringe white, a marginal line of dark dots and 2 black
arrow heads above veins 5 and 6. Hindwing white washed with cream, cream-
buff on abdominal area ; some specimens are strongly suffused with brown all
over.
Length of forewing, $ 15-19 mm. ; expanse, 35-43 mm. Length of forewing,
5 16-22 mm. ; expanse, 37-50 mm.
Habitat. 5 $<$, 7 ?? Oued Abou January, Oued Ag'elil March, Oued
Tamoudat March, 20 kil. N. of Ideles March 1914, N. of the Hoggar Mts., Sahara
(Geyr von Schweppenburg) ; Bordj Chegga, February 1912 (Hartert and
Hilgert).
105. Euxoa doufanae (Oberth.).
Agrotis doufanae Oberthiir, Etud. Lipid. Camp, fasc. xvi. p. 90. pi. xdii. ff. 4072-4073 (1919) (Col
de Doufana Aures).
I have received 80 specimens of this rare species.
1 <$ Ain Sefra, May 1913 (W. R. and E. H.) ; 1 ? Mecheria May 1918, 1 c?
El Hamel May 1912 (Victor Faroult) ; 57 J<$, 1 ? Bou Saada May, 14 $$,
5 $$ Guelt-es-Stel May — June 1915 (V. Faroult). This was wrongly identified
by me in 1914 as mauretanica.
1C6. Agrotis suffusa (Schiff. & Den.).
Phalaena suffusa Schiffermuller and Denis, Ank. Syst. Work. Schmett. Wienergeg. p. 80 (1775)
(Vienna).
Noctua ypsilon Rottemburg, Nalurj. vol. ix. p. 141 (1770).
This widely spread insect occurs all over Mauretania. We have 311 speci-
mens from Mauretania from Guelt-es-Stel, April, May, October 1913 (V. Faroult) ;
Timassinin January, I-n-kelemet February, 30 kil. N. of Amgid February,
Amgid February, Ain Tahart February, Oued Ag'elil March, 20 kil. N. of
Ideles March 1914, north of the Hoggar Mts., Sahara (Geyr von Schweppenburg) ;
Sebdou, September 1918 (P. Rotrou) ; Oued Nca, April 1914 (Hartert and Hilgert) ;
Environs de Batna, 1911-1914 (Nelva coll.) ; Biskra, March— April 1908-1911
(W. R. and E. H.) ; Colomb Bechar February, Tilghemt April 1912 (V. Faroult) ;
Oran, April 1913 (W. R. and E. H.) ; Bou Saada April, Bordj-ben-Aneridj
October 1912 (V. Faroult) ; Sidi-bel- Abbes, September— October 1917 (M.
Rotrou); Ain Draham August— September 1911, Aflou October 1915, Ham-
mam R'hira, May 1916 (V. Faroult).
28 Novitates Zoolooicae XXVII. 1920.
lo7. Lycophotia margaritosa (Haw.).
Xochta margaritosa Haworth, Lepid. Bril. p. 218 (1809).
Mr. Oberthiir quotes Engramelle as the author, but Ernst and Engramelle
when describing species not yet described only gave French names to their insects,
and therefore they are quite inadmissible as authors, and the names given to their
species by Hiibner and others must be quoted under their respective authors.
As, however, that part of Hiibner containing his saucia was published in 1827 and
Haworth's margaritosa in 1809, this latter name must be used for the present
species.
Although fairly widespread in Mauretania, it is much rarer than the last.
We have 86 specimens from Ai'n Draham, August — September 1911 (V.
Faroult) ; Oued Hamidou, June 1912 (V. Faroult) ; Hammam R'hira, May —
June 1908-1917 (V. Faroult, and W. R. and K. J.) ; Guelt-es-Stel, May— October
1913 (V. Faroult) ; Sidi-bel- Abbes, September 1917 (M. Rotrou) ; Biskra March
1909, El Kantara May 1909 (W. R. and E. H.) ; Blida les Glacieres, May 1905—
June 1908 (W. R., K. J., and Dr. Nissen) ; Environs d' Alger, May— June 1906-
1912 (W. R. and K. J. and Dr. Nissen) ; Mazagan, Morocco, January — June
1900-1903 (W. Riggenbach); Bou Saada April 1911, Djebel Aissa May 1915
(V. Faroult) ; Environs de Batna (Nelva coll.) ; Tlemcen, August 1917 (M.
Rotrou).
108. Euxoa trux trux (Hiibn.).
Noctua trux Hiibner, Samml. Eur. Schmett. A'ocf. ff. 723, 725, 770 (1S26).
This is a very variable insect, the aberrations terranea Frey, amasina and
olivina Stdgr. occur in Mauretania quite abundantly. The subspecies lunigera
Steph. appears to be confined to Great Britain.
Our series from Mauretania consists of 562 specimens from Guelt-es-Stel,
September — October 1919 (V. Faroult); Aflou, September 1916; Ai'n Sefra
July 1915, Perregaux October 1915 (V. Faroult) ; Sidi-bel-Abbes September
1917, Les Pins June 1918 (M. Rotrou); Lambessa October 1915, Batna
1909-1915 (A. Nelva coll.); Hammam R'hira July 1916, Mecheria May 1918
(V. Faroult); Sebdou July, Foret de Tenira September 1918 (P. Rotrou);
El Mahouna, September 1919 (V. Faroult).
In the British Museum, 2 33 Batna, Staudinger and Bang-Haas.
109. Euxoa segetum (Schiff. and Den.).
Phalaena segeium Schiffermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. pp. 81, 252. ff. 3
a. h. (1775) (Vienna).
Our Mauretanian series of this common insect numbers 764 specimens from
Guelt-es-Stel May— November 1912-1913, Aflou October 1916 'V. Faroult) ;
Colomb-Bechar March, April 1912, Bou Saada April 1912, Tilghemt April
1912 (V. Faroult); Mazagan, Morocco, Imitanaut, May— July 1900-1904 (W.
Riggenbach); Khenchela, May 1912 (W. R. and K. J.); Jakouren Kabylie
June 1909, El Kantara March 19C9 (W. R. and E. H.) ; Batna, June—July 1912-
1915 (Nelva coll.) ; Ain Draham, July — September 1911 (V. Faroult) ; Hammam
R'hira, July 1916 (V. Faroult) ; Sidi-bel-Abbes, September— October 1917 (M.
Novitates Zoolooicae XXVII. 1920. 29
Rotrou) ; Lambessa, 1912 (Nelva coll.) ; Alger, January 1914 (V. Faroult) ;
Djebel Antar, May 1918 (Faroult) ; Biskra, March— April 1908, 1914 (W. R. and
E. H.) ; Setil, S. of Biskra, March 1917 (V. Faroult) ; Djebel Zaccar Miliana, June
— August 1916 (V. Faroult) ; Bordj-ben-Aneridj October, Tilghemt April 1912
(V. Faroult) ; Laghouat, March 1912 (V. Faroult) ; Ideles Haggar Mts., March
1914 (Geyr von Schweppenburg) ; Sebdou, July 1918 (P. Rotrou).
In British Museum, 1 <J Mogodor, Leech coll.
109a. Euxoa cos cycladum (Stdgr.).
Agrotis cos var. cycladum Staudinger, Hot. Soc. Enlom. Ross. vol. vii. p. 121. 1. 1. f. 9 (1870) (Naxos).
We have received 1 $ of this species from Mauretania ; Mr. Oberthiir records
a series of 30 from Lambessa.
1 $ Guelt-es-Stel, May 27, 1913 (V. Faroult).
110. Euxoa rotroui sp. nov. (PI. XVII. f. 11.)
This new species is exactly intermediate in appearance between Euxoa radius
and E. trux.
$. Antennae serrate, brown ; head pale pinkish mauve ; tegulae darker with
dark brown edge ; patagia and rest of thorax pinkish mauve ; abdomen wood
grey-
Forewing pinkish mauve, basal one-fourth above vein 1 dark brownish mauve,
an oblique transverse convex dentate line of same colour separated from this deeper
coloured patch ; a darker brown mauve patch surrounding reniform stigma from
which a shadow line runs straight to inner margin ; post-median convex dentate
blackish line ; post-discal area clouded with brownish mauve.
Hindwing white with nervures, costal and abdominal areas suffused with
mouse-grey.
Length of forewing, 16 mm.; expanse, 37 mm.
1 $ Sidi-bel-Abbes, May 1918 (M. Rotrou) ; 1 $ Oran, April 1913 (W. R.
and E. H.).
111. Euxoa constanti (Mill.).
Agrotis constanti Milliere, Icon. vol. i. p. 165. pi. 9. ff. 1, 2 (1860) (Ardeche).
This species is very rare in Algeria. I have only 5 Mauretanian examples.
1 cJ Guelt-es-Stel, October 1912 (Victor Faroult) ; 4 <J<£ Environs de Batna,
October 1912-1914 (A. Nelva coll.).
112. Euxoa eos (Oberth.).
Agrotis constanti eos Oberthiir, Etud. Lipid. Comp. fasc. vii. p. 672. pi. cxci. Nos. 1841, 1847
(1913) (Aflou).
This species was supposed to be the Algerian representative of constanti, but
Mr. Oberthiir in Fasc xvi. altered his opinion, and accorded the insect specific
rank. As I have received typical constanti with grey-clouded hindwings and
creamy-buff forewings from Algeria, I feel sure he is right.
10 specimens Guelt-es-Stel, October 1912-1913 (V. Faroult).
30 NOVITATES ZOOLOGICAE XXVII. 1920.
113. Euxoa christophi (8tdgr.).
Agrotis christophi Staudinger, Berl. Entom. Zeit. 1870, p. 110 (Sarepta).
I have received 1 1 specimens of this species, 1 of which = ab. lugens Stdgr.
and 1 an intermediate aberration.
6 33, 3 $? Environs de Batna, July 1911-1914 (A. Nelva coll.) ; 1 3 Khen-
chela, May 1912 (W. R. and K. J.) ; 1 <J GuehVes-Stel, May 1913 (V. Faroult).
114. Euxoa tritici (Linn.).
Phalaena tritici Linnaeus, Faun. Suec. p. 320 (1761) (Sweden).
It is very strange to find this essentially northern insect inhabiting Southern
Algeria, where however it must be very rare.
1 ? Metlili, N. of Laghouat, September 1917 (V. Faroult).
115. Euxoa obelisca (Schiff. & Den.).
Phalaena obelisca Schiffermiiller and Denis, Ank. Syst. Werlc. Schmelt.Wienergeg. p. 80 (1776) (Vienna).
Euxoa obelisca and E. bugeaudi are very closely allied, and when among
a series of obelisca abnormal specimens occur, it is difficult to assign them correctly.
The Tring series contains 79 Mauretanian examples from Guelt-es-Stel,
October — November 1912-1913 (V. Faroult) ; Environs de Batna and Lambessa,
October 1911-1915 (A. Nelva coll.) ; Sidi-bel- Abbes, September— October 1917
(M. Rotrou); Foret de Tenira, October 1918 (P. Rotrou).
116. Euxoa bugeaudi bugeaudi (Oberth.).
Agrotis bugeaudi Oberthur, Etud. Lipid. Comp. fasc. xvi. p. 94. pi. xdiii. Nos. 4080, 4081 (1919)
(Aflou).
The series at Tring consists of 84 specimens from Guelt-es-Stel, October
1912-1913 (V. Faroult) ; Sidi-bel-Abbes, September— October 1917 (M. Rotrou) ;
Sebdou May, Foret de Tenira October 1918 (P. Rotrou).
117. Euxoa bugeaudi islyana (Oberth.).
Agrotis bugeaudi islyana Oberthur, Etud. Lipid. Comp. fasc. xvi. p. 95. pi. xdiii. Nos. 4082, 408:)
(1919) (Lambessa).
In the form from the Aures Mts. the red colour is almost always absent,
though similar grey specimens occur sporadically with the typical Central and
West Algerian form.
The Tring series contains 91 Mauretanian specimens from Environs de Batna
and Lambessa, 1911-1915 (A. Nelva coll.) ; El Mahouna, September 1919
(V. Faroult).
118. Euxoa hastifera abdallah (Oberth.).
Agrotis hastifera abdallah Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 94. pi. xdiii. Nos. 4078, 4079
(1919) (Lambessa).
I have received very few examples of this species.
5 33, 5 $$ Environs de Batna and Lambessa, July — September 1910-1915
(A. Nelva and V. Faroult).
NOVITATES ZOOLOQICAE XXVII. 1920. 'A I
119. Euxoa mauretanica (Bang-Haas).
Agrotis maurelanica Bang-Haas, Iris, vol. xxiv. p. 36. pi. iii. f. 4 (1910) (Sud Oranaie).
The series from Algeria at Tring contains 324 specimens from Tilghemt,
April 1912 (V. Faroult) ; Ghardaia, April 1911 (W. R. and E. H.) ; Bou Saada,
April 1912 (V. Faroult) ; Oued Nca, April 1914 (Hartert and Hilgert).
In the British Museum are 1 J, 1 $ South Oran, Staudinger and Bang-Haas.
120. Euxoa robiginosa (Stdgr.).
Agrotis robiginosa Staudinger, Iris, vol. vii. p. 271 (1894) (Palestine).
Of this very rare insect I have received 1 specimen from Algeria. (1 <J from
Palestine is in the British Museum and 1 $ at Tring from the same country).
1 J Environs de Batna (A. Nelva coll.). This is unique from Mauretania.
121. Euxoa powelli (Oberth.).
Agrotis powelli Oberthiir, Elud. Lipid. Comp. lasc. vi. p. 334. pi. cxxviii. ff. 1146, 1147 (1912)
(Geryville).
I have 1 1 Algerian specimens.
1 (J, 10 ?$ from Guelt-es-Stel, May 1913 (V. Faroult) ; Ain Sefra, May 1913
(W. R. and E. H.) ; Oued Hamidou, June 1912 (V. Faroult).
122. Euxoa cursoria (Hiifn.).
Phalaena cursoria Hufnagel, Berl. Mag. vol. iii. p. 416 (1766).
Of this species also I have received a single specimen, unique for Mauretania.
1 $ Bou Saada, May 1912 (V. Faroult).
[Euxoa distinguenda (Led.).
Agrotis distinguenda Lederer, Noel. Eur. p. 221 (1837) (Wallis and Altai).
I have not received this species from Mauretania. Mr. Oberthiir records it
from Lambessa.]
123. Euxoa oranaria (Bang-Haas).
Agrotis oranaria Bang-Haas, Iris, vol. six. p. 133. pi. 5. f. 9 (1906) (Sud Oranais).
This is an extremely abundant and variable species.
The series at Tring numbers 1,084 from Guelt-es-Stel, April — June 1913 (V.
Faroult) ; Bou Saada, March— May 1912 (V. Faroult) ; Ain Sefra, May 1913-
1915 (W. R. and E. H., and V. Faroult) ; Ghardaia and Oued Nca, May — June
1912 (Hartert and Hilgert); El Mesrane June 1913, Tilghemt April 1912,
Mecheria June 1918 (V. Faroult) ; Khenchela, May 1912 (W. R. and K. J.).
123a. Epipsilia simulatrix (Gey.).
Noctua simulatrix Hiibner-Geyer, Samml. Europ. Schmett. Noct. f. 712.
I have only received two of this species from Mauretania. Mr. Oberthiir
records it from Bone under the name of nictymera Boisd.
1 cJ, 1 $ El Mahouna, May 1919 (V. Faroult).
32 Novitates Zoological XXVII. 1920.
124. Euxoa lucipeta (Schiff. & Den.).
Phalaena lucipeta Schiffermiiller and Denis, Auk. FSyst. Work. Schmett. Wien Geg. p. 71 (1775) (Vienna).
I possess only 1 $ of this species taken by myself.
1 2 Blida les Glacieres, June 1908 (W. R. and K. J.).
125. Lycophotia photophila (Guen.).
Agrotis photophila Guenee, Hist. Nat. Ins. Lipid, vol. v. Noct. vol. i. p. 302 (1852) (B6ne).
Guenee described this insect from a $, so if ignipeta Oberth. is really distinct
it must always remain doubtful which of the two is the true photophila.
The series at Tring consists of 101 specimens. 42 ,$<$, 48 $$ Ain Sefra,
May^Tune, 1913-1915 (W. K. and E. H., and Faroult) ; 1 <J Msila, May 1915
(V. Faroult) ; 10 <$$ Oued Nea, April 1914 (Hartert and Hilgert).
++
[Lycophotisa ignipeta (Oberth.).
Agrotis ignipeta Oberthiir, Etud. Entom. fase. i. p. 45. pi. 4. £. 4 (1876) (El-May).
Mr. Oberthiir and Mr. Culot describe this insect as having a similar wing
pattern to photophila, but differing in the male in having the basal half of the
antennae strongly pectinated ; while the J of photophila has simple cylindrical
antennae. I have no specimen agreeing with this description, and from Mr.
Oberthiir's statement (Etud. Lipid. Comp. fasc. xvi. p. 98) he appears only to
possess the (J type captured at El-May by M. Warion in 1868.]
126. Euxoa celsicola gueddelanea (Oberth.).
Agrotis celsicola var. gueddelanea Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 99. pi. xdiii. f. 4084
(1919) (Djebel Gueddelane, Lambessa).
I have only one pair of specimens from Algeria, but these are very much
larger than any of the 65 specimens taken by myself and Dr. Jordan in 1908
at La Grave and Le Lautaret in the Hautes Alpes.
Expanse, 45 mm. ; largest specimen from Le Lautaret, 37 mm.
1 (J, 1 $ Sebdou, July 1918 (P. Rotrou).
127. Euxoa kaaba (Oberth.).
Agrotis kaaha Oberthiir, Etud. Lipid. Comp. fasc. xvi. pp. 99. pi. xdiii. Nos. 4085, 4086 (1919)
(Geryville).
I have one $, which however is not so dark as the $ figured by Oberthiir and
has the hindwings as in his (J.
1 $ Batna (Nelva coll.).
128. Euxoa radius radius (Haw.).
Bombyx radius Haworth, Lep. Brit. p. 119 (1803).
This insect, which is exceedingly abundant in Mauretania, appears in two
local subspecies, radius radius Haw. in Central and West Algeria and radius
erythroxylea Treit. in Tunisia and East Algeria.
Our series of radius radius contains 700 specimens from Algeria and Morocco,
from Biskra, February— April 1908-1916 (W. R. and E H., and Faroult) ; Bir
Novitates Zoologicae XXVII. 1920. 33
Djefair, south of Biskra, March 1909 (W. R. and E. H.) ; Environs d' Alger (Dr.
Nissen) ; Mazagan and neighbourhood, Morocco, February — March 1902-1903
(W. Riggenbach) ; Bir Setil, south of Biskra, March 1917 (V. Faroult) ; Bordj
Chegga, March 1917 (V. Faroult); Environs de Setii, 1911 (V. Faroult);
Environs de Batna (Nelva coll.) ; El Mesrane November, Guelt-es-Stel April —
November 1912-1913 (W. R. and K. J., and Faroult) ; Lalla Marnia March-
April, Oudjda and Zoudj-el-Beghal, Morocco, November 1914 (V. Faroult) ;
Sidi-bel- Abbes, September, October 1917 (M. Rotrou) ; Bou Saada March — May,
Tilghemt April 1912, Aflou October 1916 (V. Faroult) ; Perregaux, October
1915 (V. Faroult) ; Sebdou, May 1918 (P. Rotrou).
129. Euxoa radius erythroxylea (Treit.).
Noctua erythroxylea Treitschke, Schmett. Eur. vol. v. pt. iii. p. 31 (1825).
This insect which is a fixed local subspecies in Tunisia appears also spora-
dically as an aberration in Algeria, and in Sidi-bel-Abbes is the prevailing form.
I have 26 specimens from Sidi-bel-Abbes, of which 21 are erythroxylea, 1 inter-
mediate and 4 typical radius.
Euxoa radius erythroxylea comes as sole form as far west as Hammam Mes-
koutine, is the prevailing form at Batna, and occurs sporadically in other parts
of Algeria. I have none from Morocco, all mine from there being r. radius.
The series at Tring from Ain Draham to Hammam Meskoutine contains 150
specimens as follows: 113 Ain Draham, September 1911 (Victor Faroult) ; 19
Souk Ahras April, 5 Hammam Meskoutine April 1914 (W. R. and K. J.) ;
13 El Mahouna, September 1919 (V. Faroult).
In addition to these we have at Tring sporadic specimens of this form as
follows : 5 Batna (Nelva coll.) ; 1 Environs d' Alger, April 1913 (W. R. and E. H.) ;
1 Hammam R'hira, April 1912 (W. R. and K. J.) ; 2 Perregaux, October 1915 (V.
Faroult) ; 21 Sidi-bel-Abbes, September — October 1917 (M. Rotrou).
From Oran we have 5 $$ of gigantic size and of the black aberration, which
for the present I will name ab. major ab. nov. Length of forewing, 20 mm. ;
expanse, 46 mm. Length of largest $ erythroxylea , 17 mm. ; expanse, 39 mm.
5 ?$ Oran Town, April 1913 (W. R. and E. H.).
Both in radius radius and radius erythroxylea the aberration with black-brown
forewings occurs commonly.
130. Euxoa imperator (Bang-Haas).
Agrotis imperator Bang-Haas, Iris, vol. xxvi.'p. 142. pi. vi. f. 6 (1912) (Biskra).
This fine species Mr. Oberthiir considers an exaggerated form of melanura
Koll. This is not the case, as imperator is a true Euxoa while melanura is a true
Agrotis sensu Hampson and therefore widely separated.
We never found this species very abundant, and most of the material at
Tring is Central Saharan.
We have 38 specimens from Ain Sefra, May 1913 (W. R. and E. H.) ; Bou
Saada May, Djebel Kerdada May 1911-1912 (V. Faroult) ; Biskra (Staudinger) ;
north of El Golea May, Oued el Far, south of Fort Miribel May, South Oued
Mya May, Central Sahara, 1912 (Hartert and Hilgert).
In the British Museum is 1 ^ Constantine, Staudinger and Bang-Haas.
3
34 NOVITATES ZOOLOGICAE XXVII. 1920.
131. Agrotis nona 0 berth.
Agrotis nona Oberthur, EtwI. Lipid. Comp. fasc. vii. p. 62. pi. cxci. ff. 1840, 1846 (1913) (Afiou).
I have only received this from Guelt-es-Stel.
33 Guelt-es-Stel, October— November 1913 (V. Faroult).
[Epilecta linogrisea lutosa (Stdgr.).
Agrotis linogrisea var. lutosa Staudinger and Rebel, Cat. Lepid. Pal. edit. iii. p. 135 (1901) (Andalusia),
I have never received this species from Mauretania. Mr. Oberthur received
1 specimen from Khenchela.]
132. Agrotis orbona (Hiifn.).
Phalaena orbona Hiifnagel, Berl. Mag. vol. iii. p. 304 (1767) (Berlin).
There is considerable confusion in our literature in connection with the two
closely allied species we now call Agrotis orbona (Htifn.) and Agrotis comes (Treitr.).
This confusion has arisen because both species have received the names orbona
and subsequa. A. orbona (Hiifn.) was called sttbsequa by Schiffermuller in the
Wiener Verzeichniss (1775) ; A. comes (Treit.) was called orbona by Fabricius
in the Mantissa Insectorum (1787) and subsequa by Esper in the Schmetlerlinge
Europas (1786). Guenee quotes Rottemburg, Naturforscher, vol. ix. (1776), as the
author of his orbona, and as Rottemburg, in the place quoted, was criticising
Hiifnagel's work, orbona of Guenee is certainly true orbona Hiifn. ; while his
subsequa and consequa appear doubtful. Mr. Oberthur, however, appears to have
applied the name of orbona Rott.-Guen. to comes, if we may judge by the localities
he gives and from his having many variable specimens ; for while I have 31
specimens of comes from Mauretania from a number of localities, I have only two
true orbona with the conspicuous black subapical spot.
1 <J Guelt-es-Stel, October 1913 (V. Faroult) ; 1 $ El Mahouna, September
1919 (V. Faroult).
133. Agrotis comes (Treit.).
Nocliia comes Treitschke, Schmett. Eur. vol. v. pt. i. p. 254 (1825).
Triphaena orbona Oberthur (nee Hiifnagel), Etud. Lipid. Comp. fasc. xvi. p. 101 (1919) (Ain.
Draham, Lambessa).
This is much the more common of the two species, in fact after pronuba it
is the commonest of the 6 " Yellow Underwings " found in Algeria.
The Mauretanian series at Tring consists of 32 specimens from Guelt-es-
Stel, October— November 1912-1913 (V. Faroult); Ain Draham and Tunis
August — September 1911, Hammam R'hira June, north side of Djebel Zaccar
August 1916 (V. Faroult) ; Batna (Nelva coll.) ; Sidi-bel- Abbes, June —
September 1917 (M. Rotrou) ; Sebdou, June 1918 (P. Rotrou).
Mr. Warren calls orbona Hiifn. subsequa Schiff. and comes Treit. orbona
Hiifn. in Seitz Grossschmelterlinge tier Erde.
NOVITATES ZOOLOGICAE XXVII. 1920. 35
134. Agrotis pronuba (Linn.).
Plw.lae.na pronuba Linnaeus, Syst. Nat. edit. x. p. 512 (1758) (Sweden).
This is very common in some parts of Mauretania, and as variable as in
Europe.
The Mauretanian series at Tring comprises 21 1 specimens from Guelt-es-Stel,
April— October 1912-1913 (V. Faroult) ; Environs de Batna, June— October
1911-1914 (Nelva coll.) ; Environs d'Alger, May 1908 (W. R. and E. H.) ;
Hammam R'hira May — July 1916, Ain Draham August— October 1911, El
Hamel May 1912, Oued Hamidou June 1912, Bordj-ben-Aneridj October
1912, Bou Saada May 1912, Boghari May 1913, Tilghemt April 1912, Sidi
Bou Medine June 1917 (Victor Faroult) ; Khenchela, May 1912 (W. R. and
K. J.) ; Oran Town, April 1913 (W. R. and E. H.) ; Sidi-bel-Abbes June— Sep-
tember 1916-1918, Titen Yaya June 1915 (M. Rotrou) ; Lalla Marnia, Decem-
ber 1914 (V. Faroult) ; Mazagan, Morocco, October 1902 (W. Riggenbach) ;
Sebdou, June 1916 (P. Rotrou) ; Aflou, October 1916 (V. Faroult) ; El Aoudj,
July 1918 (P. Rotrou) ; El Mahouna, September 1919 (V. Faroult).
In the British Museum is 1 $ El Kantara, April 1913, P. A. Buxton.
135. Triphaena janthina intermedia subsp. nov.
Mr. Oberthiir records specimens from Marseilles intermediate between typical
janthina and his janthina algirica, and I have such specimens collected by
Georg Kriiger in Sicily. Mr. Oberthiir also records a worn specimen from Lam-
bessa of this intermediate race approaching nearest to j. janthina.
I have 1 1 specimens from Sidi-bel-Abbes which in size and marking of fore-
wings are similar to j. janthina ab. rufa Tutt, but the hindwings have a much
narrower black border, though not quite so narrow as in j. algirica. I therefore
describe this intermediate race as janthina intermedia.
3 (JcJ, 7 ?$ Sidi-bel-Abbes, August— September 1916-1917 (M. Rotrou) ;
1 <$ Ain Draham (V. Faroult).
[Triphaena janthina algirica Oberth.
Triphaena janthina var. algirica Oberthiir, Etud. Lepid. Comp. fasc. xvi. p. 102. pi. xdiii. f. 4087
(1919) (Alger).
I have no specimen of this form.]
136. Triphaena fimbria (Linn.).
Plialaena fimbria Linnaeus, Syst. Nat. edit. xii. p. 842 (1767).
I have only received two $t$ specimens of this insect.
1 J Ain Draham, July 1911 (V. Faroult) ; 1 $ Ain El-Berd, September 1918
(P. Rotrou).
137. Agrotis c. nigrum (Linn.).
Phalaena c. nigrum Linnaeus, Syst. Nat. edit. x. p. 516 (1758) (Sweden).
I have not found this so rare in Algeria as Mr. Oberthiir believes it to be.
Our Mauretanian series at Tring consists of 119 specimens from Blida les
Glacieres, June 1908 (W. R. andK. J.) ; Hammam R'hira, May— June 1908-1916
36 Novitates Zoologicae XXVTI. 1920.
(W. R. and K. J. , and Faroult) ; Environs d' Alger, March— May 1906-1911 (W. R.
and K. J. and E. H., and Dr. Nissen) ; Djebel Zaccar, Miliana, June 1916 (Victor
Faroult) ; Blida February 1916, Oued Hamidou June 1912 (V. Faroult) ; Sidi-
bel-Abbes, September 1917 (M. Rotrou) ; Foret de Tenira, June 1918 (P. Rotrou) ;
Ain Draham, July— October 1911; Masser Mines, June 1914 (V. Faroult);
El Mahouna, June 1919 (V. Faroult).
138. Agrotis flammatra (Schiff. & Den.).
Phalaena flammatra Schiffermuller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 80 (1775)
(Vienna).
Our series at Tring from Mauretania is small : 12 specimens from Ain Sefra,
May 1913 (W. R. and E. H.) ; Sebdou, June 1918 (P. Rotrou) ; Mecheria June
1918, Djebel Aissa May 1915 (Victor Faroult) ; GuehVes-Stel, October 1913
(Faroult).
139. Agrotis leucogaster (Frr.).
Noctua leucogaster Freyer, Neue Beitr. Schmett. vol. i. p. 38. pi. 21 (1831) (Prag).
Of this species I have received 7 specimens from Tunisia.
4 (?(?, 3 $$ Ain Draham, August— September 1911 (V. Faroult).
Mr. Oberthur does not record it.
140. Agrotis nisseni Rothsch. (PI. XVII. f. 18.)
Agrotis nisseni Rothschild, Novit. Zool. vol. six. p. 125. No. 2 (1912) (Ain Draham).
This fine large species appears to be very rare. Besides my 4 specimens, I
know of only one other sent for identification to Sir George Hampson by Herr
Piingler of Aachen. This species is nearest to atlantica Warr., but the ground-
colour is entirely grey and wood-brown, not red and olive as in atlantica.
1 <$, 2 ?$ Ain Draham September 1911, 1 $ Guelt-es-Stel October 1913
(Victor Faroult).
141. Agrotis augnroides Rothsch. (PI. XVII. f. 17.)
Agrotis augnroides Rothschild, Novit. Zool. vol. xxi. p. 320. No. 92 (1914) (Guelt-es-Stel).
The type has remained unique.
1 <J Guelt-es-Stel, April 1912 (W. R. & K. J.).
142. Agrotis xanthographa (Schiff. & Den.).
Phalaena xanthographa Schiflermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 83 (1775)
(Vienna).
A common insect.
I have 360 Mauretanian examples from Ain Draham, September 1911 (V.
Faroult); Batna, September— October 1912-1914 (Nelva coll.); Perregaux,
October 1915 (V. Faroult); Sidi-bel-Abbes, .September 1917 (M. Rotrou);
Foret de Tenira, September 1918 (P. Rotrou) ; El Mahouna, September 1919
(V. Faroult).
N0VITATE8 ZOOLOGICAE XXVII. 1920. 37
[Lycophotia margaritacea (Vill.).
Noclua margaritacea de VilJers, Linn. Enlom. Faun. Suec. Descr. vol. ii. p. 272. No. 340. pi. 5. f. 16
(1789) (Europe).
I have not received any insect agreeing with margaritacea, but Mr. Oberthiir
states that the insects he places under this name are more slaty coloured and are
therefore duskier than European margaritacea. I am almost convinced that he
has wrongly identified the specimens, and that he really has examples of the insect
I named Euxoa lycophotioides, and which Sir George Hampson has examined
and places in the genus Epipsilia. If this is so, and I am tolerably certain it is,
then Lycophotia margaritacea does not occur in Algeria, and the insect so-called
by Mr. Oberthiir is Epipsilia lycophotioides Rothsch.]
143. Epipsilia lycophotioides (Rothsch.). (PI. XVII. fi. 28, 29.)
Euxoa lycophotioides Rothschild, Novil. Zool. vol. xxi. p. 319. No. 81 (1914) (Guelt-es-Stel).
I have not received this species from any other locality.
15 <J,J Guelt-es-Stel, October 1912-1913 (V. Faroult).
144. Agrotis praecipuina (Rothsch.). (PI. XVII. f. 9.)
Epipsilia praecipuina Rothschild, Novit. Zool. vol. xxi. p. 321. No. 97 (1914) (Guelt-es-Stel).
I have only received 8 specimens in all of this species which at first sight
looks like a xanthograplia washed all over with bright rufous.
1 $ Guelt-es-Stel, September 1913 (V. Faroult) ; 3 $<$, 1 $ Ain Draham, Sep-
tember 1911 (V. Faroult) ; 3 ^ Sidi-bel- Abbes, September 1917 (M. Rotrou).
145. Epipsilia faceta (Treit.).
Noclua faceta Treitschke, Schmett. Eur. vol. x. pt. ii. p. 35 (1835).
The Tring series contains 91 Mauretanian specimens from Environs d' Alger,
January— December 1906-1912 (W. R., E. H., Dr. Nissen, Captain Holl, and
Faroult) ; Hammam R'hira February 1918, Blida February 1916 (V. Faroult) ;
Rabat (A. Thery).
In the British Museum are 2 $$ Tangier ; 1 $ Mauretania, Staudinger and
Bang- Haas ; 1 $ Hammam Meskoutine, March 1911, Meade Waldo.
146. Amathes witzenmanni (Standi).
Orthosia witzenmanni Standfuss, Mitth. Schweiz. Enlom. Gesell. vol. viii. p. 233 (1890) (Digne).
I have very few specimens of tliis fine species, 10 (J<J, 5 ?$, of which 6 cJ(J are
ab. plumbina Tnr., 2 $$, 2 $$> ab. griseola Rothsch., 2 <$£, 2 $$ ab. castanea
Rothsch., and 1 $ dark grey entirely suffused with vinous red which I name ab.
griseovinosa ab. nov.
7 cJcJ Environs de Batna, 1911-1914 (Nelva coll.) ; 3 $$, 5 ?$ Guelt-es-Stel,
October — November 1912-1913 (V. Faroult). I have not any of the ab. vinosa
Oberth.
38 Novitates Zoolooicae XXVII. 1920.
147. Monima stabilis (Schiff. & Den.).
Phalaena stabilis Schiffermiiller and Denis. Ank. Sijst. Werk. Schmeit. Wienergeg. p. 76 (1775) (Vienna).
I have only 1 Algerian specimen of this species, which appears to be very
rare in Mauretania.
1 $ Environs d' Alger, March 30th, 1911 (W. R. and E. H.).
| Monima cruda (Schiff. & Den.).
Phalaena cruda Schiffermiiller and Denis, Ank. Syst. Werk. Schmeit. Wienergeg. p. 77 (1775) (Vienna).
I have no Mauretanian examples of this species. Mr. Oberthiir records it
from Lambessa.]
148. Amathes ruticilla (Esp.).
Noctua ruticilla Esper, Schmetl. pt. iv. vol. ii. p. 525. No. 220. pi. clvii. (Noct. 78) f. 1. (1791)
(Florence).
I have received very few of this species.
6 cJ(J, 4 ?$ Environs de Batna, 1913-1914 (Nelva coll.).
149. Amathes lychnidis (Schiff. & Den.).
Phalaena lychnidis Schiffermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 76 (1775)
(Vienna).
Phalaena pistacina Schiffermiiller and T)enis,Ank.Syst. Werk. Schmett. Wienergeg. p. 77 (1775) (Vienna).
I have 29 Mauretanian specimens from Environs de Batna, 1910-1914 (A.
Nelva and V. Faroult) ; Hammam R'hira, February — .June 1918 (V. Faroult) ;
Sidi-bel-Abbes, June 1918 (M. Rotrou) ; Environs d' Alger, January 1911 (W. R.
and E. H.) ; Blida, December 1915 (Faroult). 1 specimen is ab. coernlescens
Calb.
150. Amathes lota (Linn.)
Phalaena lota Linnaeus, Syst. Nat. edit. x. p. 513 (1758).
Of this species the Mauretanian examples at Tring number 19 from Batna.
12 <$<$, 5 ?9 Environs de Batna, October 1910-1914 (A. Nelva and V. Faroult) ;
1 cJ Blida February 1916, 1 ? Aflou October 1916 (V. Faroult).
151. Amathes macilenta (Haw.).
Noctua macilenta Haworth, Lepid. Brit. p. 239 (1809).
I have received 1 specimen of this species.
1 ? Aflou, October 21st, 1916 (V. Faroult).
152. Sidemia fissipuncta oberthuri subsp. nov.
This is the insect Mr. Oberthiir has treated of as Orthosia ypsilon Schiff., but
ypsilon Schiff. being preoccupied by ypsilon Rott., Haworth's name fissijmncta
is the correct appellation. I have it treated as a subspecies at present, but
believe it will prove a distinct species. Mr. Oberthiir says that the Algerian
form appears to be very pale in colour and have the pattern much effaced ; but
that he has too few specimens to confirm this.
NOVTTATES ZOOLOOIOAE XXVII. 1920. 39
The series from Algeria at Tring consists of 63 specimens, 20 from East
Algeria and 43 from West Algeria, and they are very distinct from European and
British examples.
<J 9 differs from fissipuncta fissipuncta in being much paler, in the markings
being less pronounced, in the submarginal band being much straighter and less
sinuate, and in the postmedial band being well developed in most specimens and
much nearer the reniform.
14 <$£, 16 99 Environs de Batna, 1911-1912 (A. Nelva coll.) ; 17 <$<$, 18 $$
Sidi-bel-Abbes and Les Trembles, April— July 1914-1918 (M. Rotrou) ; 2 <J<J,
5 99 Sebdou and Foret de Tenira, May— June 1 91 8 (P. Rotrou) ; 1 <J Lalla Marnia,
April 1914 (V. Faroult).
Type $ Sidi-bel-Abbes.
153. Omphaloscelis Iunosa (Haw.).
Noctua Iunosa Haworth, Lepid. Brit. p. 230 (1809).
I have received very few Mauretanian examples of this species.
1 <J, 4 99 Guelt-es-Stel, October— November 1913 (V. Faroult) ; 5 $$, 1 9
El Mesrane November 1913, 3 <$<$, 1 $ Aflou October 1916 (V. Faroult).
[Amathes haematidea (Dup.).
Noctua haematidea Duponchel, Lepid. France, vol. vii. p. 363. pi. 122. f. 5 (1827) (France).
I have no Mauretanian examples.]
[Amathes litura (Linn.).
Phalaena litura Linnaeus, Faun. Suec. edit. ii. p. 320 (1761) (Sweden).
Also of this species I have no specimens from Mauretania.]
154. Amathes helvola (Linn.).
Phalaena helvola Linnaeus, Syst. Nat. edit. x. p. 507 (1758) (Finland).
Phalaena rufina Sehffermuller and Denis, Ank. Syst. Werk. Schmelt. Wienergeg. p. 86 (1775) (Vienna).
Guenee, and consequently Oberthiir also, attributes the name rufina to
Linnaeus and quotes " S. IT. 72." What this reference means I have been unable
to trace, nor can I find any such name as rufina in Linnaeus. Rufina Schiffermiiller
is described in the Wiener Verzeichniss, 1 775, so is much later than Linnaeus'
helvola 1758.
1 have 2 99 from Algeria of the red form.
2 $$ Environs de Batna, 1913-1914 (Nelva coll.).
155. Amathes lucida (Hiifn.).
Phalaena lucida Hiifnagel, Berl. Mag. vol. iii. p. 302 (1767).
The name nitida Schiff., used by Mr. Oberthiir, was published in 1775, eight
years later than Hiifnagel's lucida.
I have 2 Algerian specimens.
1 cJ Hammam R'hira, February 1918 (V. Faroult) ; 1 9 Environs de Batna,
1913-1914 (A. Nelva coll.).
40 NOV1TATE8 ZOOLOOICAE XXVII. 1920.
I Conistra silene (Schiff. & Den.).
Phalaena silene SchifFermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 85 (1775) (Vienna).
I have not received this insect from Mauretania.]
[Conistra veronicae (Hiibn.).
Noclua veronicae Hiibner, Samm. Europ. Schmett. Noct. i. 541 (1827).
This also is not in the Tring Museum from Mauretania.]
[Conistra erythrocephala (Schiff. & Den.).
Phalaena erythrocephala Schiffermuller and Denis, Ank. Syst. Werk. Schmett. Wiemrgeg. p. 77 (1775)
(Vienna).
Again this species has never come to hand from Mauretania.]
156. Conistra vaccinii sebdouensis (Aust.).
Orrhodia sebdouensis Austaut, Lc Natur. 1880. p. 221 (Sebdou).
The Algerian race, although just as variable as the European and British
vaccinii vaccinii, is constantly different and is a well separated subspecies.
I have 27 Algerian specimens from Environs de Batna, October 1910-1914
(A. Nelva and V. Faroult).
[Xantholeuca croceago (Schiff. & Den.).
Phalaena croceago Sehiffermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 86 (1775) (Vienna).
This species we have not received.]
157. Cosmia austauti (O berth.).
Xanlhia atistauti Oberthiir, Elud. Enlom. fase. vi. p. 87. pi. 1. f. 3 (1881) (Sidi-bel-Abbes).
Sir George Hampson unites this with palleago Hiibn., but I consider it a
distinct species ; it differs at first sight from palleago by the much rounder and
blunter apex of the forewings, in fact its shape is much more that of gilvago
Schiff.
This is very variable indeed, and the following aberrations have names ; pale
nankeen as in type, but pattern heavy and brownish = ab. monilifera Culot ;
orange-cinnamon with heavy sooty pattern = ab. batnensis Culot ; rosy cinnamon
or rufous cinnamon, pattern not heavy = ab. algirica B.-H. (1912) = rosina
Culot (1914).
Our Mauretanian series at Tring numbers 216, from Environs de Batna,
October 1909-1914 (A. Nelva, Faroult, and Staudinger) ; Bou Saada March 1912,
Aflou October 1916, Lalla Marnia November 1914 (Victor Faroult) ; Foret de
Tenira, October 1918 (P. Rotrou) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ;
Bordj-ben-Aneridj, October 1912 (V. Faroult); Medjes October 1911, Aflou
October 1916 (V. Faroult) ; Guelt-es-Stel, November 1913 (V. Faroult).
The British Museum has 2 £<$, 2 $<j> Batna, Staudinger and Bang-Haas.
Novitates Zoolooicae XXVII. 1920. 41
158. Cymatophora algirica (Culot).
Cirrhoedia algirica Culot, Noel, et Gkom. d"Eur. pt. i. vol. ii. p. 76. pi. 53. f. 1. (1914) (Lambessa).
I have of this Mauretanian species 46 specimens — viz. 25 Sidi-bel-Abbes,
October 1917 (M. Rotrou) ; 1 (J Batna (Staudinger) ; 19 Foret de Tenira Octo-
ber, 1 Sebdou September 1918 (P. Rotrou).
The latter specimen was sent out as Cirrh. pallida var. ; pallida Stdgr. is
quite a different insect from Asia Minor and has pure white hindwings.
[Enargia ulicis Stdgr. and its allies. Mr. Oberthiir makes all the forms of
Enargia, occurring in Algeria, forms of one species, ulicis Stdgr. Sir George
Hampson, on the other hand, makes them out to be 3 good species. It is very
difficult to decide this question, because it is complicated by the occurrence of
3 distinct colour groups in each form : (1) Yellowish ochre grey = ab. griseo-olivacea
Culot. (Form 2) Salmon to deep brick-red = ab. rufa Culot. (Form 3) Brown to
black-brown = ab. brunnea Culot. I consider therefore my series too small to
decide these points, and shall for the present follow Sir George Hampson and
treat them as 3 species.]
159. Enargia ulicis (Stdgr.).
Cosmia ulicis Staudinger, Stett. EnUmi. Zeit. 1859. p. 214 (Granada).
1 2 from Guelt-es-Stel (V. Faroult) ; 2 JJ, 6 22 El Mahouna, September 1919
(V. Faroult).
160. Enargia regina (Stdgr.).
Cosmia regina Staudinger, Iris, vol. iv. p. 297. pi. 4. f. 2 (1892) (Asia Minor).
1 have 1 2 very large and typical from Ain Draham, September 1911 (V.
Faroult).
The British Museum has 1 $ Le Tarf, D. Lucas.
161. Enargia algirica Culot.
Enargia algirica Culot, Noct. et Giom. a" Eur. p. 73. pi. 52. ff. 9, 10 (f. 8 appears to be an aberrant
regina) (August 1914) (Lambessa).
Amathes rufescentior Rothschild, Novit. Zool. vol. xxi. p. 331. No. 163 (October 1914) (Guelt-es-Stel).
The Tring series consists of 20 <$<$, 18 $2 : 3 $<$ Batna, September 1913
(Nelva coll.) ; 1 2 Lambessa, 1912 (Nelva coll.) ; 15 (J<J, 15 22 Guelt-es-Stel May
1913, 1 J Ain Draham September 1911 (V. Faroult) ; 1 $, 2 22 El Mahouna,
September 1919 (V. Faroult).
2 (JcJ, 1 2 are the ab. griseo-olivacea Culot, and 1 <J, 2 22 are the ab. ruberrima
Rothsch.
The British Museum has 2 <?<?, 2 22 Guelt-es-Stel ex Tring Museum.
162. Enargia jordani sp. nov. (PI. XVII. f. 27.)
Nearest allied to borjomensis Stdgr., but differs in the orbicular and reniform
being both strongly developed. It also differs at a glance in the antennae being
so strongly serrate as to be almost pectinated while the 22 of all the other species
have simple antennae.
42 Novitates Zoolooicae XXVII. 1920.
?. Antennae rufous brown ; head and thorax rufous cinnamon ; abdomen
whitish grey, freckled heavily with black scales.
Forewings rufous cinnamon, freckled with black scales ; antemedian line not
strongly marked, reniform and orbicular very large, dark brown, postmedian
line clearly defined and well marked sinuate and strongly dentate ; fringe entirely
rufous cinnamon not edged with black as in vlicis and allies. Hindwing dull
white ; a minute black stigma and a median sinuate angulate pale cinnamon line.
Length of forewing, 18 mm. ; expanse, 41 mm.
1 ? Souk Ahras, April 15th, 1914 (W. R. and K. J.).
163. Miselia luteago (Schiff. & Den.).
Phalaena luteago SchifTcrmiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 86 (1775) (Vienna).
(In Cat. Brit. Mus. as Polia.)
I have only two Mauretanian specimens. 2 $$ Hammam R'hira, May 1916
(V. Faroult).
164. Hydroecia xanthenes orientalis (Oberth.).
Jortijria xanthenes var. orientalis Oberthur, JSlud. Lepid. Comp. fasc. xvi. p. 127. pi. xdv. f. 4105
(1919) (Batna).
Most of my specimens are much paler than the figured type.
1 have 1 2 Mauretanian specimens : 3 $<$, 5 $$ Lamberidi nr. Batna
October 1910, 1 <J Bordj-ben-Aneridj October 1912, 1 $ A'in Draham October
1911, 1 (J Hammam R'hira February 1918, 1 $ Blida November 1S15 (Victor
Faroult). Most of the specimens are very large, especially the 9?, considerably
larger than European specimens.
165. Epipsilia straminea (Rothsch.). (PI. XVII. f. 10.)
Euxoa straminea Rothschild, Novit. Zool. vol. xxi. p. 318. No. 80 (1914) (Guelt-es-Stel).
2 <JtJ Guelt-es-Stel, October 1912 (V. Faroult).
166. Parastichtis monoglypha (Hiifn.).
Phalaena monoglypha Hiifnagel, Berl. Mag. vol. iii. p. 308 (17G7) (Berlin).
The Tring series from Mauretania is very small, 13^, 9$?: 11 c?c?> 4 $$
Batna 1909 (A. Nelva coll.) ; 1 <J, 3 ?? Hammam R'hira April— May 1917, 1 $
Bordj-ben-Aneridj October 1912 (V. Faroult) ; 1 <J, 1 $ El Mahouna, July 1919
(V Faroult).
167. Pseudohadena chenopodiphaga (Ramb.).
Mamestra chenopodiphaga Rambur, Ann. Soc. Entom. France, vol. i. p. 283. pi. 9. i. 7 (1832) (Corsica).
The Mauretanian series at Tring consists of 67 specimens from Guelt-es-Stel,
April — November 1914 (W. R. and K. J., and Faroult) ; Bordj Ferjan and Bordj
Mecht-el-Kaid, east of Touggourt, April 1909 (W. R. and E. H.) ; Bou Saada and
Tilghemt April— May 1912, Am Sefra May 1915, El Mesrane May 1913,
Biskra May 1910 (Victor Faroult) ; Khenchela, May 1912 (W. R. and K. J.) ;
north of El Golea, March 1912 (Hartert and Hilgcrt) ; Mecheria, May 1918
(Faroult).
Novitates Zoolooicae XXVII. 1920. 43
The ab. erubescens Stdgr. occurs all over Algeria amongst the type, but most
frequently in the south.
The British Museum has 1 $ Hammam-es-Salahin, April 1904, Lord
Walsingham.
168. Pseudohadena roseonitens (Oberth.).
Mamestra roseonitens Oberthiir. Bull. Soc. Enlom. France. 1887. p. 49 (Biskra).
Of this fine insect I have 12 specimens from Khenchela, May 1912 (W. R.
and K. J.) ; Bou Saada, May 1911 (V. Faroult) ; Biskra (Staudinger) ; Bordj
Chegga, S. of Biskra and Zaatscha, W. of Biskra, April 19C9 (W. R. and E. H.).
169. Saragossa seeboldi arabum Culot.
Saragossa seeboldi var. arabum Culot, Noct.el Giom. il'Eur. pt. i. vol. i. p. 112. pi. 19. f. 12 (1911)
(Sebdou).
Of this very rare species I have only 5 Algerian specimens.
1 <$ Batna (Nelva coll.); 1 $ Guelt-es-Stel, September 1913 (W. R. and
K. J.) ; 1 J, 1 ? Sidi-bel-Abbes, September 1917 (M. Rotrou) ; 1 <$ Bou Yousuf,
September 1914 (A. Nelva).
170. Hadula pulverata (B.-H.).
Mamestra pulverata, Bang-Haas, Iris, vol. xx. p. 71. pi. iii. f. 8 (1907) (Gafsa).
Polia cinnamomeogrisea Rothschild, Novit. Zool. vol. xx. p. 121. No. 36 (1913) (Boriij Chegga).
The series at Tring consists of 58 specimens from Bordj Chegga. Bordj
Saada, and Kef-el-Dohr, S. of Biskra, February 1912 and March 1917 (Kartert
and Hilgert, and V. Faroult).
I only found out that cinnamomeogrisea = pulverata after the whole article
was written.
171. Hadula griseola (Rothsch.).
Odonlelia griseola Rothschild, Novit. Zool. vol. xx. p. 121. No. 37 (1913) (halfway between Ouargla
and El Golea).
This insect appears to be rare ; only 2 further specimens in addition to the
original 5 have come to hand.
4 <3<S (including type of ab. rosacea) Mraier S. of Biskra, 1 $ halfway
between Ouargla and El Golea February — March 1912, 1 <$ Hassi Dinar S. of
Touggourt (Hartert and Hilgert) ; 1 $ Bir Stil, S. of Biskra, March 1917 (V.
Faroult).
172. Margelana irritaria (B.-Haas).
Apamea lestacea var. irritaria Bang-Haas, Iris, vol. xxvi. p. 146 (1912) (Batna).
This insect has been much confused ; Bang-Haas has placed it as a sub-
species of Pallti perina lestacea Hiibn., Culot does not mention it, and Oberthiir
places it as one of the many varieties he attributes to his Palluperina dayensis.
Sir George Hampson, however, declares that structurally it is not a Palluperina
at all, but a Margelana.
I have 17 $<$ all from Batna, including 1 co-type.
17 $$ Batna, 1909-1914 (A. Nelva).
In the British Museum is 1 $ Batna, Staudinger and Bang-Haas.
44 Novitates Zooxogicae XXVII. 1920.
173. Palluperina powelli (Culot).
Apamea nickerlii var. powelli Culot, Noct. el Qkom. d'Eur. p. 140. pi. 25. f. 10 (5) (1912) (Geryville).
Luperina pseudoderthisa Rothschild, Novit. Zool. vol. xxi. p. 332. No. 170 (1914) (Guelt-es-Stel).
1 have 15 specimens of this species.
5 33 Aflou October 1916, 4 33, 2 $$ Guelt-es-Stel September— October 1913
(V. Faroult) ; 1 $ Sebdou, September 1918 (P. Rotrou) ; 1 3 Sidi-bel- Abbes,
September 1917 (M. Rotrou) ; 1 3, 1 ? El Mahouna, September 1919 (V. Faroult).
174. Palluperina nickerlii graslini Oberth.
Luperina nickerlii var. graslini Oberthur, Bull. Soc. Entom. France, 1908, p. 323 (Pyrenees-Orientales).
This subspecies is the form found in Algeria ; I have 15 specimens.
2 JcJ, 1 $ Batna October 1910-1914 (Nelva and Faroult) ; 5 33, 2 $$ Aflou,
October 1916 (V. Faroult); Sebdou, September 1918 (P. Rotrou); 1 $ Sidi-
bel-Abbes, September 1917 (M. Rotrou) ; 2 33 El Mahouna, September 1919
(V. Faroult).
Mr Oberthur remarks that his Algerian specimens are paler and greyer than
Mr. Culot's figure plate 25 f. 9, but mine are almost as dark, except the Sidi-bel-
Abbes $ and 1 Batna 3-
175. Palluperina dayensis (Oberth.).
Luperina rubella var. dayensis Oberthur, Etud. Entom, fasc. vi. p. 80. pi. 11, i. 9 (1881) (Daya).
Mr. Oberthur unites under dayensis all the forms of the teshicea section from
Algeria. My series of testacea, rubella, etc. from all localities are too few for me
to express an opinion, and so I have followed Mr. Oberthur in this instance.
The series from Algeria at Tring contains 42 specimens from Environs de
Batna, September 1909-1914 (A. Nelva) ; Sidi-bel-Abbes, Messer, September —
October 1917 (M. Rotrou) ; Foret de Tenira, September 1918 (P. Rotrou) ;
Sebdou, September 1918 (P. Rotrou) ; Guelt-es-Stel October 1912, Biskra
November 1910 (V. Faroult) ; El Mahouna, September 1919 (V. Faroult).
176. Palluperina dumerilii (Dup.).
Noclua dumerilii Duponchel, Lipid. France, vol. vi. p. 277. pi. 90. f. 4 (1826) (France).
I have 3 33, 4 $$ of this species, 1 § being of the ab. armoricana.
1 3, 1 $ A'in Draham October 1911, 1 3 Aflou October 1916, 1 $ Perregaux
November 1915 (V. Faroult) ; 1 3 Environs de Batna, 1913-1914 (A. Nelva) ;
1 $ Foret de Tenira, September 1918 (P. Rotrou) ; 1 $ El Mahouna, September
1919 (V. Faroult).
177. Sidemia fulva (Rothsch.). (PI. XVII. ff. 20, 21.)
Meganephira oxyacanthae fulva Rothschild, Novit. Zool. vol. xxi. p. 329. No. 151 (1914) (Guelt-es-Stel).
We now have at Tring 1 1 33, 6 ?$ of this species : 6 33, 2 ?$ El Mesrane,
November 1913 (V. Faroult) ; 3 33, 2 $$ Perregaux, September — October 1915
(V. Faroult) ; 1 $ (type) Guelt-es-Stel, October 1912 (V. Faroult) ; 1 3 Biskra,
March 1914 (W. R. and E. H.).
Novitates Zoolooioae XXVII. 1920. 45
178. Dasysternum faroulti sp. nov. (PI. XVII. f. 22.)
$. Antennae greyish white ; head and thorax greyish sandy-cinnamon ;
abdomen greenish buff.
Forewing greyish sandy-cinnamon ; orbicular reduced to a point, reniform
large white bordered inwardly with brown ; antemedian line strongly angled
three times dark cinnamon brown, postmedian line strongly dentate-lunate
running obliquely inwards, antemedian line basad and postmedian line distad
bordered with white ; submarginal line white ; fringe chequered and lined with
white. Hindwing dirty whitish grey, whiter towards termen, marginal hair-
line brown.
Length of forewing, 19 mm. ; expanse, 44 mm.
1 $ El Mesrane, November 1915 (V. Faroult).
179. Dasythorax rotroui sp. nov. (PI. XVII. f. 23.)
$. Antennae dark brown, cylindrical ; head, thorax, and abdomen cinnamon
wood-brown.
Forewing cinnamon brown, freckled with black scales ; an incomplete ante-
median line obliquely outwards to vein 2, orbicular with black ring and central
dot, reniform large whitish, a curved dentate postmedian black line, post-discal
area strongly irrorated with black scales. Hindwing milk white.
Length of forewing, 15 mm. ; expanse, 34 mm.
1 $ Messer, September 1917 (M. P*otrou).
180. Namaugana chimaera sp. nov. (PI. XVII. f. 24.)
This curious species is unlike any other Noctuid known to me.
,$. Entirely wood-grey, with an intense satiny sheen. Forewing irrorated
slightly with black scales, basal one-fifth more thickly, an oblique faint black
hair-line from vein 1 outwards towards apex to vein 5, a submarginal row of
black indistinct spots from vein 4 to inner margin.
Length of forewing, 14 mm; expanse, 31 mm.
1 {J Environs de Taourirt, Morocco, July 1918 (per M. Rotrou).
181. Sidemia aflouensis sp. nov. (PI. XVII. f. 25.)
Nearest to kostantschikovi Piingl.
<$. Antennae amber-brown ; head and thorax slaty mouse-grey ; abdomen
yellowish grey. Forewing slaty mouse-grey, orbicular and reniform indistinct,
claviform prominent ; a dentate curved postmedian thin line, black pale grey on
distad side. Hindwing white.
Length of forewing, 15 mm. ; expanse, 34 mm.
1 <J Aflou, October 1916 (V. Faroult).
182. Thalpophila vitalba (Frr.).
Noctua vitalba Freyer, Neue Beitr. vol. ii. pt. xxi. p. 48. pi. 124. fit. 3, 4 (1834) (Sicily).
I have a series from Mauretania of 23 specimens : Am Draham, September
1911 (V. Faroult) ; Environs d' Alger, September 1908 (Dr. Nissen and Captain
Holl) ; El Mahouna, September 1919 (V. Faroult).
46 Novitates Zoolooicae XXVII. 1920.
183. Trachea secalis (Linn.).
Phalaena secalis Linnaeus, Syst. Nat. edit. x. p. 519 (1758) (Sweden).
This is one of the most variable of species, and has an enormous distribution
from Great Britain in the west to Japan in the east, from Scandinavia in the
north to Mauretania in the south, and in Asia from the Arctic Ocean in the north
to India in the south.
Mr. Oberthiir remarks that he has never seen a specimen of the ab. struvii
Ragusa from Mauretania ; it certainly must be extremely rare there, but I have
one very fine strongly marked specimen of this aberration from Setif.
The series of Mauretanian examples at Tring consists of 209 specimens
from Berrouaghia, April 1914 (V. Faroult) ; Sidi-bel- Abbes, September — October
1917 (M. Rotrou) ; Environs de Setif, 1911 (V. Faroult) ; Lambessa, November
1912 (A. Nelva coll.) ; A'in Draham, August — September 1911 (V. Faroult) ;
Environs de Batna (A. Nelva coll.).
184. Procus faroulti (Rothsch.).
Bryophila faroulii Rothschild, Novit. Zool. vol. xxi. p. 333. No. 177 (1914) (Guelt-es-Stel).
Mr. Oberthiir has described this insect under the name of Miana erratricula
poicelli, but, as Sir George Hampson pointed out to me, the median and post-
median lines run differently to those in erratricula , and he considers this a distinct
species. Sir George Hampson also considers I was right originally in placing it
in the genus Bryophila and not in that of Procus (Miana), but I am more than
doubtful of this now, and prefer to treat it as a species of Procus.
The Tring series consists of 42 specimens from Guelt-es-Stel, August —
September 1913 (V. Faroult).
185. Procus furuncula (Schiff. & Den.).
Phalaena furuncula Schiffermiiller and Denis, Ank. Sysl. Werk. Schmett. Wienergeg. p. 89 (1775)
(Vienna).
This insect appears to be rare in Mauretania, as I have received only 4 3<S,
3 $$.
1 <J, 2 $$ Sidi-bel-Abbes, September 1917 (M. Rotrou) ; 1 $ Foret de
Tenira, September 1918 (P. Rotrou) ; 1 ^ Ain Draham, August 1911 (V. Faroult) ;
2 3$ Metlili, September 1917 (V. Faroult).
18C. Miselia carpophaga (Borkh.).
Phalaena carpophaga Borkhausen, Eur. Schmett. vol. iv. p. 422 (1792).
Mr. Oberthiir places this species under the name of capsophila Dup. It is
quite true that most of my Mauretanian specimens are ab. capsophila, but it
cannot be treated as a separate species or subspecies, as it occurs everywhere
with the type.
We have at Tring 69 specimens from Sebdou, May 191S (P. Rotrou) ; Bou
Saada, May 1912 (V. Faroult) ; Souk Ahras, April 1914 (W. R. and K. J.) ; Ham-
mam R'hira August 1916, Messer June 1918 (V. Faroult) ; Batna, May — June
1915 (A. Nelva coll.) ; Khenchela, May 1912 (W. R. and K. J.) ; Guelt-es-Stel
May 1913, Meeheria May 1918 (V. Faroult); Sidi-bel-Abbes, May 1918 (M.
Rotrou) ; Sebdou, Foret de Tenira, May 1918 (P. Rotrou).
NOVITATES ZOOLOGICAE XXVII. 1920. 47
187. Pronotestra silenides (Stdgr.).
Uamestra silenides Staudinger, Iris, vol. vii. p. 273. pi. ix. f. 14 (1894) (Chiclava).
The Mauretanian series of this insect at Tring consists of 152 specimens from
Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and V. Faroult) ; Biskra,
March— April 1908-1914 (W. R. and E. H.) ; Ghardaia, April 1911 (W. R. and
E. H.) ; Bou Saada, March— April 1911-1912; Mecheria May 1918, El Kantara
March— April 1911 (Victor Faroult) ; Tilghemt, April 1911 (W. R. and E. H.) ;
Tunis, South Oran (Staudinger).
In the British Museum are 1 o1 Algeria ; 1 $ Tunis ; 1 <$ El Kantara, April
1913, P. A. Buxton.
188. Epia silenes (Hiibn.).
Noclua silenes Hiibner, Eur. Schmett. Noct. i. 653 (1827).
Polia trisagittata Rothschild, Novit. Zool. vol. xxi. p. 322. No. 104 (1914) (Guelt-es-Stel).
The darker ab. sancta Stdgr. (Dianthoecia sancta Staudinger, Slett. Entom.
Zeit. 1859, p. 213 (Chiclana)) has been placed by Sir George Hampson as an
aberration of Epia nisus Germ. ; but I agree with Messrs. Culot and Oberthiir
that it belongs to silenes Hiibn.
My irisagiUaia is a J with very strongly developed markings and with very
high colour contrasts.
Our series at Tring consists of 149 Mauretanian specimens from Guelt-es-Stel,
March — April 1912-1913 (W. R. and K. J., and Faroult) ; Hammam Meskoutine,
April 1914 (W. R. andK. J.); Bou Saada, March— April 1911-1912 (V. Faroult) ;
Batna (Nelva) ; Mazagan, March 1902 (W. Riggenbach).
[Miselia bicruris (Hufn.).
Phalaena bicruris Hufnagel, Berl. Mag. vol. iii. pt. iii. p. 302 (1707) (Berlin).
Mr. Oberthiir makes use of Schiffermiiller's name capsincola, but bicruris
has nine years' priority. I have not received this species from Mauretania.]
189. Miselia magnolii (Boisd.).
Dianthoecia magnolii Boisduval, Ind. Meth. p. 125 (1829).
My single <$ from Hammam Meskoutine has the ground-colour almost black,
with no trace of rufous colouring so conspicuous in Mr. Culot's figure (Noct. et
Geom. d'Eur. vol. i. pi. 20. f. 8).
1 <J Hammam Meskoutine, April 1914 (W. R. and K. J.).
190. Miselia compta galactina (Turati).
IHanthoecia galactina Turati, Nat. Sicil. vol. xx. p. 25. pi. 6. ff. 10, 11 (1907) (Sicily).
The Algerian form appears to be this and must be very rare, as Mr. Ober-
thiir only records it from Guelt-es-Stel, and I have only received 1 single (J also
from there.
1 J Guelt-es-Stel, June 1913 (V. Faroult).
48 NOVTTATES ZOOLOQICAE XXVII. 1920.
191. Miselia conspersa (Schiff. & Den.).
Phalaena conspersa Schiffermiiller and Denis, Ank. Syst. Werk, Schmett. Wienergeg. p. 71 (1775)
(Vienna).
Mr. Oberthiir does not record this species, but Mr. Culot does so from Morocco.
The series at Tring consists of 38 specimens from Environs d'Alger May
1908, Hammam Meskoutine, and Souk Ahras April 1914 (W. R. and K. J.) ;
Hammam R'hira August, Djebel Zaccar, near Miliana, June 1916 (V. Faroult) ;
Guelt-es-Stel, April— June 1913 (V. Faroult) ; Sidi-bel-Abbes, May 1918 (M.
Rotrou) ; El Mahouna, May — June 1919 (V. Faroult).
192. Miselia dysodea faroulti (Rothsch.).
Polia faroulli Rothschild, Novit. Zool. vol. xxi. p. 322. No. 106 (1914) (Guelt-es-Stel).
Hecatera dysodea africana Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 138 (1919) (Geryville).
Mr. Oberthiir has renamed this insect as usual, because it has not been
figured by me.
The Tring series of Mauretanian examples numbers 43 specimens from Bou
Saada April— May 1911-1912, Guelt-es-Stel September 1913 (V. Faroult);
Tamarouth, Morocco, June 1904 (W. Riggenbach) ; Environs d' Alger (Captain
Holl).
193. Miselia antitypina (Rothsch.). (PI. XVII. f. 8.)
Polia antitypina Rothschild, Novit. Zool. vol. xxi. p. 322. No. 107 (1914) (Guelt-es-Stel).
This species must be very rare, as I have only received the two <J<J from
Guelt-es-Stel.
2 <J<J Guelt-es-Stel, April 1912-1913 (W. R. and K. J., and Faroult).
194. Miselia filigrama 'Esp.).
Nocta filigrama Esper, Europ. Schmett. p. 396. No. 137. pi. 130. f. 4 (1788) (Innspruck).
I have 2 <£<£ of this species from Mauretania ; it is not recorded by Mr.
Oberthiir.
1 <J Tamarouth, W. Morocco, June 1904 (W. Riggenbach) ; 1 c? ? (Sand
coll.).
195. Miselia serena (Schiff. & Den.).
Phalaena serena Schiffermiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 84 (1775) (Vienna).
This insect is very variable and has received a number of names, but the
forms Corsica, lettconota, obscara, etc., seem to occur together with the type and
can only rank as aberrations.
I have at Tring 17 specimens from Guelt-es-Stel, April — May 1912-1913
(W. R. and K. J., and Faroult) ; Bou Saada, May 1911 (V. Faroult) ; Hammam
Meskoutine, May 1914 (W. R. and K. J.) ; Hammam R'hira, August 1916 (V.
Faroult) ; Khenchela May 1912, Biskra April 1914, Environs d' Alger May 1912
(W. R., K. J., and E. H.).
NOVITATES ZOOLOGICAE XXVII. 1920. 49
196. Metopoceras canteneri canteneri (Dup.).
Polia canteneri Duponchel, Rev. Entom. SSb. vol. i. pt. i. p. 37. pi. 3 (1S33) (S. France, Hyeres).
I thought in 1913, after comparing Guelt-es-Stel specimens with European
ones, that typical canteneri did not occur in Algeria ; but I have since received
from Messrs. Rotrou some specimens from the extreme west of the province of
Oran which are indistinguishable from Portuguese specimens. I therefore must
divide the Algerian canteneri into two local races.
Of canteneri canteneri I have at Tring 9 specimens from Les Pins, June 1918
(M. Rotrou) ; Sebdou June, Foret de Tenira May 1918 (P. Rotrou).
197. Metopoceras canteneri pallidior Rothsch.
Metopoceras canteneri pallidior Rothschild, Novit. Zool. vol. xx. p. 123 (1913) (Guelt-es-Stel).
Of this paler Central Algerian subspecies we have at Tring 4 c$<3, 3 $$.
4 <£<?, 1 o Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and Faroult) ;
2 $? Bou Saada, May 1911 (V. Faroult).
198. Metopoceras felicina (Douz.).
Polia felicina Douzel, Ann. Soc. Entom. France, ser. ii. vol. ii. p. 199. pi. 6. f. 2 (1844) (Marseilles).
Of this species we have at Tring 100 specimens from Hammam Meskoutine,
April— May 1909-1914 (W. R., E. H., and K. J.) ; Lalla Marnia, April— May,
1914 (V. Faroult) ; Oran, April 1913 (W. R. and E. H.) ; Mazagan, Morocco,
March — April 1902 (W. Riggenbach) ; Hammam R'hira, May 1908 (W. R. and
K. J.); Bou Saada April 1911, Oued Hamidou June 1912, Guelt-es-Stel April
1913 (V. Faroult) ; Sebdou, Foret de Tenira, May 1918 (P. Rotrou) ; Sidi-bel-
Abbes, May 1918 (M. Rotrou).
In the British Museum is 1 <J Forest of Marmora, April 1903, Meade-Waldo.
[Metopoceras codeti Oberth. ; Ammetopa nisseni Rothsch. ; and Ammetopa
codeti Hmpsn.
There has been a most extraordinary amount of confusion in connection
with these three insects, and it only shows how three experienced lepidopterists
like Sir George Hampson, Monsieur Oberthiir, and Monsieur Culot can be deceived
even when assisted by type specimens, good figures, and series of allied species.
Metopoceras codeti Oberth. was first described and figured from Sebdou in
1881 (Etud. Entom. livr. vi. p. 88. pi. xi. f. 10). In the description Mr. Oberthiir
says, " Taille de Felicina ; mais les ailes un peu moins elargies," i.e. less broad.
In continuation Mr. Oberthiir says that the forewings and thorax above are
strongly washed with rose. Now, I have specimens from Am Sefra and Sebdou
taken by myself and P. Rotrou which agree precisely with the original description
and figure of codeti Oberth.
In 1913 Mr. Culot published a description and figure professing also to be
codeti Oberth. {Nod. et Geom. d'Evr. pt. i. vol. i. p. 166. pi. 30. f. 18). In his
description Mr. Culot lays great stress on the narrow forewings, very sinuate and
dentate postmedian line, and the greyish median space. Now, Mr. Culot states
that his figure was taken from the " specimen typicum " of Mr. Oberthiir from
Sebdou. This I cannot believe, as the drawing is totally different from the
drawing in Etud. Entom. livr. vi., undoubtedly made from the type. More-
4
50 NOVITATES ZOOLOGICAE XXVII. 1920.
over, Mr Culot's figure is identical with Guelt-es-Stel specimens, while I have
specimens identical with the figure in the Etudes from Sebdou and Ai'n Sefra.
I feel sure that Mr. Culot received from Mr. Oberthiir a Guelt-es-Stel or El Outaya
specimen in mistake for the original Sebdou specimen caught by Dr. Codet.
Tn the Catalogue of Heterocera, vol. vi. Sir George Hampson created the genus
Ammetopa, (p. 120) for two (J insects caught by Mrs. Nicholl and Mr. Eaton at
Biskra, and which he had identified as codeti Oberth. This insect is totally
different to either codeti Oberth., codeti Culot, or nisseni Rothsch., and belongs
to a different genus. Finally, Ammetopa nisseni Rothsch. was described by me
in 1913, because I compared my Guelt-es-Stel specimens with the Biskra ones
in the British Museum, which I then thought were true codeti Oberth. I propose
to figure codeti Oberth., codeti Hmpsn., and nisseni Rothsch. on one plate to show
the differences.
The true facts are these : There are two races of codeti Oberth., one the typical
one from West Algeria (Province Oran), and the other from Central and Eastern
Algeria (Provinces Alger and Constantine). This insect does not belong to
the genus Metopoceras, but to Bryomima, and the two races must stand as Bryo-
mima codeti codeti (Oberth.) and Bryomima codeti nisseni (Rothsch.). The
insect identified by Sir George Hampson as codeti Oberth. will stand as Ammetopa
codeti Hmpsn.].
199. Bryomima codeti codeti (Oberth.). (PI. XV. ff. 22. 23.)
Metopoceras codeti Oberthiir, Etud. Entom. livr. vi. p. 88. pi. xi. f. 10 (1881) (Sebdou).
Of this form we have at Tring 4 <$S, 7 $$ from Ain Sefra, May 1913 (W. R.
and E. H.) ; Sebdou, May 1918 (P. Rotrou) ; Mecheria, May 1918 (V. Faroult).
Of these the two taken by ourselves at Ai'n Sefra are identical with Mr.
Oberth iir's type figure.
200. Bryomima codeti nisseni (Rothsch.). (Fl. XV. ff. 24, 25.)
Amtnetopa nisseni Rothschild, Novit. Zool. vol. xx. p 123 (1913) (Guelt-es-Stel).
The principal distinction between this and codeti codeti is the much sharper
and more distinct ante- and postmedian transverse bands on the forewings.
Of this form I have 19 specimens, all from Guelt-es-Stel, March — April 1912—
1913 (W. R. and K. J., and Faroult and Dr. Nissen).
201. Ammetopa codeti Hmpsn. (PI. XV. f. 21.)
Ammetopa codeti Hampson, Cat. Lepid. Phal. Brit. Mus. vol. vi. p. 120. No. 2222. fig. 32 (1906) (Biskra).
This insect must be very rare, as my solitary specimen is only the third
known.
1 (J Oued Amra, north of I deles, April 1914 (Geyr von Schweppenburg).
2 (JcJ Algeria and Biskra, March 1897 (A. E. Eaton and Mrs. Nicholl), in
British Museum.
202. Metopoceras omar (Oberth.).
Cleophana omar Oberthiir, Bull. Soc. Entom. France. 1887, p. 57 (Oued Leber, Tunis).
Of this purely Mauretanian species, the series at Tring contains 329 specimens
from Ain Sefra, May 1913 (W. R. and E. H.) ; Guelt-es-Stel, April 1912-1913
(W. R. and K. J., and Faroult) ; Bou Saada March, Laghouat March 1912,
NOVITATES ZOOLOG1CAE XXVII. 1920. 51
Djebel Kerdada May 1912 (V. Faroult) ; Tilghemt, April 1911-1912 (W. R. and
E. H., and Faroult) ; Ghardaia, April 1911 (W. R. and E. H.) ; Bordj Saada,
Bordj Chegga, Kef-el-Dohr, February 1912 and March 1917 (Hartertand Hilgert,
and Faroult) ; Biskra, March— April 1908-1914 (W. R. and E. H., and Faroult,
and Staudinger) ; El Kantara March 1911, El Hamel May 1912 (V. Faroult) ;
Constantine, Tunis (F.T.) (Staudinger) ; Khenchela, May 1912 (W. R. and K. J.) ;
Oued Nea, April 1914 (Hartert and Hilgert) ; Ai'n Sefra May 1915, Mecheria,
May 1918 (V. Faroult) ; Hammam R'hira May 1917, Bou Saada May 1911 (V.
Faroult) ; Sidi-bel- Abbes, May 1918 (M. Rotrou) ; Foret de Tenira, May 1918
(P. Rotrou).
In the British Museum are 1 <$, 1 $ Algiers ; 1 $ Biskra, March 1897, P. A.
Buxton ; 2 <$$ Hammam-es-Salahin, April 1904, Lord Walsingham.
203. Metopoceras morosa Rothsch. (PI. XV. f. 20.)
Metopoceras morosa Rothschild, Novit. Zool. vol. xxi. p. 326. No. 133 (1914) (Guelt-es-Stel).
2 $6 Guelt-es-Stel, April 1913 (V. Faroult). I have received no more of this
species, which differs from purplish varieties of omur in the antemedian band.
204. Metopoceras khalildja O berth.
Metopoceras khalildja Oberthiir, Etiid. Entom. livr. ix. p. 38. pi. 3. f. 1 (18S4) (Sebdou).
Our series at Tring consists of 120 specimens from Guelt-es-Stel, March —
April 1913 (Victor Faroult) ; Khenchela, May 1912 (W. R. and K. J.) ; Turns
(Dannehl) ; Berrouaghia and Lalla Marnia, April 1914 (V. Faroult) ; Environs
de Batna, 1911-1912 (A. Nelva coll.) ; Environs de Tunis, March— April 1915
(M. Blanc) ; Sebdou, May 1918 (P. Rotrou).
In the British Museum are 1 <£ Hammam Meskoutine, March 1911, Meade-
Waldo.
205. Scotogramma implexa (Hiibn.).
Noctua implexa Hiibner, Samml. Eur. Schmett. Noct. f. 414 (1827).
Our series at Tring consists of 225 specimens from Khenchela, May 1912
(W. R. and K. J.) ; Batna, 1909-1914 (A. Nelva coll.) ; Souk Ahras, April 1914
(W. R. and K. J.) ; Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and
Faroult) ; Sebdou, Foret de Tenira, May 1918 (P. Rotrou) ; Sidi-bel- Abbes,
May 1918 (M. Rotrou).
The British Museum has 4 Khenchela ex Tring Museum.
206. Centropodia inquinata (Mab.).
Hadena inquinala Mabille, Bull. Soc. Entom. France, 18S8, p. 43 (Gabes).
I have only received this insect from Guelt-es-Stel.
69 Guelt-es-Stel, October 1912-1913 (V. Faroult).
The British Museum has 1 <J Egypt.
207. Antitype flavicincta (Schiff. and Den.).
Plialaena flavicincta Schiffemiiiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 72 (1775)
(Vienna).
I have 55 Algerian specimens of this insect from Blida les Glacieres, October —
November 1910 (Dr. Nissen) ; Environs de Batna, 1910-1914 (A. Nelva and
52 NOVITATES ZOOLOGICAE XXVII. 1920.
Faroult) ; Sidi-bel-Abbes, November 1916-1918 (M. Rotrou) ; Hammam R'hira,
December and January 1916-1918 (V. Faroult) ; Lalla Marnia December 1914,
Lambiridi October 1910, Blida November 1915, Guillaumet December 1913
(V. Faroult).
[Antitype nigrocincta (Treit.).
Polia nigrocincta Treitschke, Schmett. Eur. vol. v. pt. 2. p. 31 (1825) (Modling, nr. Vienna).
I have never received this species from, or found it in, Mauretania.]
208. Antitype dubia (Dup.).
Polia dubia Duponchel, Lipid. France, Supp. vol. iii. p. 286. pi. 26. f. 4 (1836) (Aix).
I received a <J of this species from Monsieur A. Nelva and 1 from Monsieur
M. Rotrou.
1 (J Environs de Batna, 1911-1912 (A. Nelva coll.) ; 1 <J Sidi-bel-Abbes,
December 1916 (M. Rotrou).
209. Antitype subvenusta Piing.
Antitype subvenusta Piingler, Iris, vol. xix. p. 94 (1906) (Jerusalem).
Although this species was described from Palestine, so many Steppe and
Desert insects have a very wide distribution, that it is not very strange for it to
turn up in Algeria.
The specimens I have are all paler than the drawing made from Herr
Piingler's type, but as they are not quite fresh and vary also much inter se, I do
not venture to separate them subspecifically.
I have 12 <$<$, 1 ^ of this species.
12 (JcJ, 1 $ Environs de Batna, September 1910-1914 (A. Nelva and Faroult).
210. Antitype argillaceago deliciosa (Oberth.).
Polia venu-sta deliciosa Oberthiir, Bull. Soc. Entom. France, 1907, p. 345 (Sebdou) ; Etud. Lipid
Comp. fasc. iii. pi. xxvii. ff. 147, 154 (1909).
Mr. William Warren in Seitz (Grossschm. Erde, vol. iii. p. 136) treats this insect
as an aberration of argillaceago ; this is certainly wrong, as typical examples of
itigillaceago do not occur in Algeria. Mr. Oberthiir originally described this as a
subspecies of argillaceago Hiibn. (vetntsta Boisd. was described in 1840, and so
must sink, as argillaceago dates from 1827) ; but in 1919 (Etud. Entom. Comp.
fasc. xvi. p. 143) he treats it as a distinct species. I think the original status
attributed to this very beautiful insect by its describer is the correct one, and
therefore it is here enumerated as a subspecies of argillaceago, notwithstanding
my contrary statement in 1914 (Novit. Zool. vol. xxi. p. 330, sub No. 158 (1914)).
I have 65 <J<J and 7 $$, all from Guelt-es-Stel, of which 11 rftf, 1 $ are ab.
squamosa Rothsch. ( = f. 147 Oberthiir).
54 <$<$, 6 $$ Guelt-es-Stel, September— November 1912-1913 (V. Faroult).
ab. squamosa Rothschild, Novit. Zool. vol. xxi. p. 330, sub No. 158 (1914)
f Guelt-es-Stel).
II tJ(J, 1 $ Guelt-es-Stel, September— November 1912-1913 (Faroult).
NOVTTATES ZOOLOOICAE XXVII. 1920. £3
211. Antitype germana Rothsch.
Antitype germana Rothschild, Novit. Zool. vol. xxi. p. 330. No. 159 (1914) (Guelt-es-Stel).
Polia rosinata Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 142. pi. xdvi. f. 4119 (1919) (Guelt-es-Stel).
Mr. Oberthiir as usual has renamed my insect, because I had not figured it.
7 cJcJ, 3 $? Guelt-es-Stel, September— October 1913 (V. Faroult).
1 <J in the British Museum from same source ex Tring Museum.
212. Antitype hagar Rothsch. (PI. XVII. f. 1.)
Antitype hagar Rothschild, Novit. Zool. vol. xix. p. 125. No. 4 (1912) (Bou Saada).
2 <J(J Bou Saada, March— April 1911-1912 (V. Faroult).
213. Antitype sahariensis Rothsch.
Antitype sahariensis Rothschild, Ann. Mag. Nat. Iilbt. (8) xvi. p. 251. No. 23 (1915) (Rharis).
Polia salmonea Oberthiir, Etud. Entom. Comp. fasc. xvi. p. 142. pi. xdvi. f. 418 (1919) (Biskra).
Once more Mr. Oberthiir creates a useless synonym.
I have received 3 specimens of this rare insect ; I had completely overlooked
the Colomb-Bechar specimen.
1 <$ Colomb-Bechar, February 1915 (V. Faroult) ; 1 $ Rharis, Central Sahara.
April 1914- (Geyr von Schweppenburg) ; 1 jj Djebel Antar, May 1918 (V. Faroult),
214. Antitype discalis Rothsch.
Antitype discalis Rothschild, Novit. Zool. vol. xix. p. 125. No. 3 (1912).
1 cJ, 1 ? Batna, October 1910 and 1912 (A. Nelva and Faroult).
215. Antitype rosea Rothsch.
Antitype rebecca ab. rosea Rothschild, Novit. Zool. vol. xxi. p. 330. sub No. 157 (1914) (Guelt-es-Stel).
Epuntla concolor Oberthiir, Etud. Lipid. Comp. p. 143. pi. xdvii. ff. 4120, 4121 (1919) (Geryville).
In 1914 I wrongly identified this insect with rebecca Stdgr.
It therefore is rather unfortunate that my aberrational name rosea has to
stand for the species.
The ground-colour varies from whitish cream or bufHsh grey to rosy or
salmony cinnamon.
The ab. suffusa is densely powdered with mouse-grey scales.
I have 37 <J<J, 5 $$, all from Guelt-es-Stel.
37 <5S, 5 ?$ Guelt-es-Stel, September— October 1912—1913 (V. Faroult).
In the British Museum 2 <$■$ Guelt-es-Stel ex Tring Museum.
216. Eumichtis lichenea (Hiibn.).
Noclua lichenea Hiibner, Samml. Eur. Schmetl. Noct. ff. 562, 563 (1827).
I have 71 Mauretanian specimens from Guelt-es-Stel, October 1912-1913 (V.
Faroult) ; Environs de Batna (A. Nelva coll.) ; Aflou October 1916, Hammam
R'hira February 1918, Lalla Marnia October 1914 (V. Faroult) ; Sidi-bel-Abbes,
October — November 1917 (M. Rotrou) ; Foret de Tenira, November 1918 (P.
Rotrou) .
54 NOVJTATES ZOOLOQICAE XXVII. 1920,
217. Aporophyla chioleuca (Herr.-Sch.).
Polici chioleuca Hemch-Scliiiffer, Syst. Bearb. Schmett. Eur. vol. ii. p. 255. No. 221. Noel. pi. 16. ff. 76-
78 (1845) (S. Europe).
Sir George Hampson employs the name mioleuca Treit. [Schmett. Eur. vol. x.
Suppl. pt. ii. p. 43 (1835) (Sicily)) for this insect. There is grave doubt as to
this being correct ; Treitschke quotes his insect as being Hiibner's mioleuca,
giving Samml. Schmett. Eur. Xoct. ff. 545, 746 as the citation ; now Hiibner's
mioleuca has been quite correctly identified by Sir George Hampson as Agriopis
aeruginea Hiibn., and must stand as aeruginea mioleuca Hiibn.. or only as aetu-
ginea ab. mioleuca should it be shown that it occurs together with the type.
Moreover, Treit scke lays stress in Ins description (p. 44) on the basal area of the
forewing being marked grey and yellow, which is the case in aeruginea, but
certainly not in the Aporophyla. I am therefore convinced that mioleuca and
chioleuca Treit. (p. 46) are both referable to aeruginea Hiibn., and that the first
name available for this insect is chioleuca H.-S. Mr. Oberthur considers
mioleuca Rami), a distinct local race of chioleuca, but I feel sure it is only a more
sombre-coloured aberration.
The Tring series consists of 11 (JcJ from Hammam R'hira, December 1917
(V. Faroult); Blida March 1915, Bordj-ben-Aneridj October 1912 (V. Faroult) ;
Aflou, October 1916 (V. Faroult); Sidi-bel-Abbes, September 191S (M. Rotrou) ;
Foret de Tenira, November 1918 (P. Rotrou).
218. Aporophyla nigra (Haw.).
Noctua nigra Haworth, Lepid. Brit. p. 192 (1809).
Our series of Mauretanian examples at Tring consists of 50 specimens from
Guelt-es-Stel October — November 1913, Aflou October 1916, Lalla Marnia
November 1914 (V. Faroult) ; Sidi-bel-Abbes, November 1916 (M. Rotrou).
219. Eombycia chretieni (Rothsch.).
Calophasia chretieni Rothschild, Novit. Zool. vol. xxi. p. 327. No. 137 (1914) (Guelt-es-Stel).
Bombycia viminalis emir Oberthur, Etud. Lipid. Comp. fasc. xvi. p. 146. pi. xdvi. II. 4122, 4123 (1919)
(Sebdou, Lauibessa).
Mr. Oberthur has placed this insect as a subspecies of viminalis Fabr. and
of course renames it emir because I did not figure it.
It is certainly a distinct species and not a race of viminalis ; but it may
turn out to be angularis Chret. If, however, the drawing in the British Museum
made from Mr. Chretien's type is correct, it is not angularis, for the hindwing in
$ angularis is white and the pattern is different.
I have at Tring 9 $<$, 27 $$, viz. 2 JJ, 2 ?$ Sebdou, June 1918 (P. Rotrou) ;
1 $ Hammam Meskoutine, May 1914 (W. R. and K. J.) ; 2 ?$ Guelt-es-Stel,
May 1913 (V. Faroult) ; 1 $ Sakamodi, August 1912 (V. Faroult).
The $ from Sakamodi is different from the 5 other $$ ; the hindwings aro
nearly white, the orbicular stigma is smaller, rounder, and more distinct, and the
central one-third of the forewings is much blacker ; this is probably aiigularis
Chret.
[Valeria oleagina (Schiff. & Den.).
Bombyx olexvjina Schulerm tiller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 59 (1775) (Vienna).
I have not received this species from Mauretania.]
NOVITATES ZOOLOGICAE XXVII. 1920. 55
220. Meganephria oxyacanthae (Linn.).
Phalaena oxyacanthae Linnaeus, Syst. Nat. edit. x. p. 516. No. 113 (1758).
1 have only received 3 specimens of this insect from Algeria.
2 ^ Hammam R'hira, December 1917 and January 1918 (V. Faroult) ;
1 ^ Environs de Batna, 1914 (A. Nelva coll.).
Mr. Oberthur unites the Algerian examples with oxyacanthae benedictina
Stdgr., but my 3 specimens from Algeria are very different from all my 226 speci-
mens of o. benedictina from Amasia. The Algerian form will probably require a
new subspecific name, but I have too few to venture on this course.
[Agriopis aprilina bouveti D. Lucas.
Agriopis bouveti Daniel Lucas, Ann. Soc. Entom. France, 1905. p. 51. pi. 5. ff. 2, 3 (Le Tarf).
I have never received this.]
221. Trigonophora meticulosa (Linn.).
Pluilaena meticulosa Linnaeus, Syst. Nat. edit. x. p. 513. No. 95 (175S) (Sweden).
The Mauretanian series at Tring consists of 75 specimens from Guelt-es-Stel,
May 1913 (V. Faroult) ; Sidi-bel-Abbes, September— October 1917-1918 (M.
Rotrou) ; Environs de Batna (A. Nelva coll.) ; Am Draham September 1911,
Boghari May 1913, Hammam R'hira March 1916 (V. Faroult).
222. Rhizotype fiammea (Esp.).
Bombyx fiammea Esper, Schmelt. vol. iii. p. 269. No. 79. pi. 53. f. 3 (1785) (South Italy).
Mr. Oberthur uses Hubner's name of empyrea for this species, because he
says the name fiammea has been applied to so many noctuids. As, however, they
all belong to different genera and subfamilies, the danger of mistakes is not so
formidable as Mr. Oberthur thinks ; certainly in this case it cannot justify the
discarding of a name which has 32 years' priority over that of Hiibner.
My Algerian material is very poor, 1 8 <$<$, 5 ?? from Lambessa and Environs
de Batna, October 1912-1914 (A. Nelva coll.) ; Sidi-bel-Abbes, November 1917
(M. Rotrou) ; Foret de Tenira, October 1918 (P. Rotrou).
223. Rhizotype crassicornis obscura (Oberth.).
Phlogophora crassicornis obscura Oberthur, Etud. Lipid. Comp. fasc. xvi. p. 152. pi. cdlxxxii. ff.
3974, 3975 (1919) (Lambessa).
Mr. Oberthur on pages 148-152 gives an elaborate history of jodea H.-S.
and very clearly points out the differences between the present species and that
one. While both jodea and crassicornis occur together in Europe, in Mauretania
only crassicornis occurs. Mr. Oberthur points out also that Algerian crassicornis
differs considerably from those of Digne ; he, however, only names a $ aberration
of it. As the whole of the Algerian crassicornis are different from typical Digne
specimens, Mr. Oberthiir's aberrational name becomes the subspecific nime,
and the Mauretanian form must be called Rhizotype. crassicornis obscura (Oberthur).
The Tring series is very poor, 16 rJJ, 4 $$ from Lambessa and Batna,
October 1912-1914 (A. Nelva coll.).
56 Novitates Zoolocicae XXVII. 1920.
224. Euplexia lucipara leonhardi Rebel.
Euplexia leonltardi Rebel, Verk. Zool. Bot. Gesell. Wim, vol. 59. p. 331. No. 1. text fig. 2 (1909)
(Alma).
Of this species the Tring series of Mauretanian examples consists of 129
specimens from A'in Draham, August — September 1911 (V. Faroult) ; Environs
d' Alger, March- April, 1906-1911 (W. R. and E. H. and Dr. Nissen) ; Guelt-es-
Stel September 1913, Environs de Setif 1911 (V. Faroult). This is a darker,
duskier local subspecies, but the pattern differences given by the author are
not confirmed in my series of 129 specimens.
225. Polyphaenis xanthochloris graslini C'ulot.
Polyphaenis xanthochloris var. graslini C'ulot, Noel, el Geom. a" Ear. pt. i. vol. i. p. 200. pi. 37. f. 5 (1913)
(Castille).
My two Mauretanian specimens agree well with Culot's figure of the
Castille specimen, allowing for the difference of sex.
1 (J Ai'n Draham, September 1910 (V. Faroult) ; 1 <$ El Mahouna, September
1919 (V. Faroult).
226. Luperina leucophaea (Schiff. & Den.).
Phalaena leucophaea Schiffermiiller and Denis, Ante. Syst. Werlc. Schmelt. Wienergeg. p. 82 (1775)
(Vienna).
This insect is stated b}- Mr. Oberthiir to be very abundant near Lambessa,
but I have only received 2 specimens.
2 £3 Environs de Batna, 1914 (A. Nelva coll.).
227. Scotogramma sodae rosacea subsp. nov.
Mr. Oberthiir states that Algerian examples of sodae Ramb. are much more
rose-coloured than French examples. This is a constant character, and so I have
named this form rosacea.
Our series consists of 27 examples from El Mesrane June 1913, Bou Saada
May 1911 (V. Faroult) ; Biskra, March— April 1908-1914 (W. R. and E. H.).
The British Museum has 1 q Gafsa, Tunisia, 1913, G. C. Champion; 1 3
Hammam-es-Salahin, April 1904, Lord Walsingham.
228. Scotogramma trifolii cinnamomina Rothsch.
Scotogramma cinnamomina Rothschild, Xovit. Zool. vol. xx. p. 121. No. 36 (1913) (Nza-ben-Rzig).
The Mauretaman examples are all more rosy-cinnamon, less grey, in tint
than European ones, and so my name, given to an extra strikingly coloured
specimen, must stand for the subspecies.
Sir George Hampson and others have united with the typical form of this
species treitschkei Boisd. ; this is, however, erroneous, as the genitalia are very
different ; treitschkei is identical with Hiibner's pugnax, so this species will have
to stand as Scotogramma pugnax (Hiibn.).
The Mauretanian series at Tring consists of 285 specimens from Bou Saada
April— May 1911-1912, Laghouat and Tilghemt April 1912, El Kantara March-
April 1911, Environs de Setif 1911 (V. Faroult) ; Ghardaia May 1912, Oued
NOVITATES ZoOLOGICAE XXVII. 1920. 57
Nca April 1914, Sands of El Arich May 1912, Mraier February 1912 (Hartert
and Hilgert) ; Bordj Chegga, March 1917 (V. Faroult) ; Biskra March — April
1908-1909, Bordj Saada April 1909 (W. R. and E. H.) ; Environs de Batna,
1913-1914 (A. Nelva coll.) ; Khenchela, May 1912 (W. R. and K. J.) ; Hammam
Meskoutine, May 1914 (W. R. and E. H.) ; Ain Draham, September 1911 (V.
Faroult) ; Hammam R'hira, May 1908-1913 (W. R., E. H., and K. J.) ; Perregaux
October 1915, Aflou October 1916, Guelt-es-Stel May— November 1912-1913
(V. Faroult) ; Sidi-bel- Abbes, June- August 1916-1917 (M. Rotrou) ; Mecheria
June 1918, Ain Sefra May 1914, Colomb-Bechar March— April 1912 (V. Faroult) ;
Foret de Tenira October 191S, Tlemcen August 1918 (P. Rotrou) ; Environs de
Taourirt, Morocco, July 1918 (M. Rotrou).
The British Museum has 1 $ Algeria, Mrs. Nicholl.
229. Scotogramma chimaera sp. nov. (PI. XVII. f. 6.)
(J. Differs from t. cinnamomina in its large size, bright sandy cinnamon ground-
colour, proportionately narrower wings, very large and rounded reniform stigma,
and the black submarginal band on the fore wings. On the hind wings all the
veins are picked out in blackish grey.
Length of forewing, 19 mm. ; expanse, 43 mm.
1 <$ Ain Sefra, March 1915 (V. Faroult).
230. Cardepia deserticola Hmpsn. (PI. XVII. ff. 2, 3.)
Cardepia irrisor ab. deserticola Hampson, Cat. Lepid. Phal. Brit. Mus. vol. v. p. 235, sub No. 1457,
1905 (Syria).
Cardepia affinis Rothschild, Novit. Zool. vol. xx. p. 122. No. 40 (1913) (Kef-el-Dohr).
Sir George Hampson when diagnosing his new genus Cardepia gave as the
principal difference the reniform truncate and strongly protruding frontal
prominence, which was excised below. I may add from examination at Tring
that this prominence has a distinct rolled edge or rim.
Now Sir George Hampson places in this genus Cardepia two species,
irrisor Ersch. and nova Smith.
Under irrisor he describes from Syria an aberration under the name ab.
deserticola. I have a number of specimens agreeing with his ab. deserticola from
the desert regions of Algeria, all showing the strongly developed reniform frontal
process, with a distinct rolled rim.
When, however, Dr. Jordan examined our Ural and Turkestan irrisor, he
found that the frontal prominence was quite different, being round, flatter, and
devoid of the rolled rim.
We found 12 specimens, mostly from the Central Hauts Plateaux of Algeria,
agreeing in the shape and morphology of the frontal prominence with irrisor. It
therefore becomes quite clear that at least two species have been confounded
under the name irrisor, and they must for the present stand as Cardepia irrisor
(Ersch.) (PI. XVII. f. 4) and Cardepia deserticola Hmpsn.
Of deserticola we have at Tring 30 Mauretanian specimens from El Outaya
March 1911, Bou Saada May 1910, 1911, Guelt-es-Stel March, El Mesrane
June 1913, Colomb-Bechar March— April 1912 (V. Faroult) ; Bordj Chegga,
February— March 1912 and 1917 (Hartert and Hilgert, and Faroult) ; Kef-el-
58 « NOVTTATES ZOOLOOICAE XXVII. 1920.
Dohr, February 1912 (Hartert and Hilgert) ; Bir Djefair, March 1909 (W. R. and
E. H.).
The British Museum has 2 £$, 1 $ Hammam-cs-Salahin, February — April
1904, Lord Walsingham.
231. Cardepia irrisor mauretanica subsp. 'nov. (PI. XVII. f. 5.)
^$. Differ from irrisor irrisor in having rounder shorter wings, in the ground-
colour of the forewings being browner less whitish, and in the hindwings being
much less white. The pattern on the forewings is also much less distinct.
9 $$, 1 $ El Mesrane, June 1913 (V. Faroult) ; 1 £ Bou Saada, May 1912 (V.
Faroult) ; 1 ^ Khenchela, May 1912 (W. R. and K. J.) ; I J Perregaux, Sep-
tember 1915 (V. Faroult).
This species has the frontal process rounded, and the rolled rim found in
deserticola is absent.
232. Miselia oleracea variegata (Aust.).
Mamwlra variegata Austaut, Le Nat. ser. i. vol. vii. p. 142 (1885) (Oudjda).
Monsieur Oberthiir is quite right when he says that the ground-colour of
the Mauretanian race is vinous maroon rather than reddish ochraceous. He
is also right in saying that the late Mr. Warren had not any accurate knowledge
of the Mauretanian form of oleracea. I find under ab. variegata Aust. in the col-
lection at Tring (the part arranged by Mr. Warren), 7 specimens from the
Issykul and Thian Shan regions agreeing exactly with the figure in Seitz of
variegata, i.e. of a greyish ochraceous colour, while Mr. Warren had placed 7
Mauretanian examples among the series of typical oleracea.
The Tring series of oleracea variegata (vera) consists of 104 specimens from
Hammam R'hira, May 19CS-1917 (W. R. and K. J., and Faroult) ; Environs
d' Alger, March— May 1907-1911 (W. R. and E. H., and Dr. Nissen) ; Environs
de Setif, 1911 (V. Faroult) ; Mazagan, Morocco, February 1903 (W. Riggenbaeh) ;
A'in Draham, August— September 1911 (V. Faroult) ; Sidi-bel- Abbes, Messer,
September 1917 (M. Rotrou) ; Environs de Taourirt, Morocco, July 1918 (M.
Rotrou) ; Souk Ahras, April 1914 (W. R. and K. J.) ; El Mahouna, June 1919
(V. Faroult).
233. Eumichtis solieri (Boisd.).
Hadena solieri Uoisduval, I ml. Meth. p. 120 (1S40) (Provence, Sicily).
Our series from Mauretania consists of 198 specimens from Mazagan and
Mhoiwla, Morocco, October 1902, Seksawa, Morocco, April 1905 (W. Riggenbaeh) ;
Oudjda, Morocco, November 1914 (V. Faroult) ; Lalla Marnia, November 1914
(V. Faroult) ; Foret de Tenira, October 1918 (P. Rotrou) ; Sidi-bel- Abbes
September— October 1917 (M. Rotrou) ; Bou Saada, March 1912 (V. Faroult),
February— March 1908 and 1916 (W. R. and E. H., and Faroult) ; El Kantara,
Biskra, March— April 1911 (W. R. and E. H., and Faroult) ; Lambiridi, October
1910 (V. Faroult) ; Lambessa and Environs de Batna, 1911-1914 (A. Nelva coll.) ;
Hammam Meskoutine, April 1914 (W. R. and E. H.) ; A'in Draham, September —
October 1911 (V. Faroult); Bordj-ben-Aneridj, November 1911 (V. Faroult);
Hammam R'hira, January— May 191 1-1918 (W.R., E. H., and K. J., and Faroult) ;
Environs d'Alger, March— May 1907-1912 (W. R., E. H., and K. J., and Dr.
Nissen) ; El Mahouna, September 1919 (V. Faroult).
NOVITATES ZOOLOGICAE XXVII. 1920. 59
234. Parastichtis arabs arabs (Oberth.).
Hadena solieri var. (ou aberr.) arabs Oberthiir, Elud. d'Entom. livr. vi. p. 88. pi. xi. f. 8 (1881)
(Sebdou).
Mr. Oberthiir quite rightly says that standfussi Turati and ribbei Piingl. are
only local subspecies of arabs ; of which there are now 5 subspecies described :
(1) arabs arabs Oberth., (2) arabs biskrae Oberth., both confined to Algeria, the
first in the Hauts Plateaux region, the second in the Desert Zone ; (3) arabs
standfussi Turati ; (4) arabs ribbei Piingl. ; (5) arabs polyglypha Stdgr. Of the
three latter we know No. 3 from Sicily and the coast region near Alger, while
No. 4 is so far known only from Spain and No. 5 is known only from Palestine.
Of arabs arabs we have at Tring 28 specimens from Sebdou, May 1918 (P.
Rotrou) ; Khenchela, May 1912 (W. R. and K. J.) ; Batna, May 1915 (A. Nelva
coll.).
235. Parastichtis arabs standfussi (Turati).
Hadena standfussi Turati, Nat. Sic. vol. xx. p. 27. pi. vi. ff. 17, 18 (1908) (Busambra).
This form is at once recognisable by its much greyer ground-colour, though
not so clear grey as in arabs ribbei.
Described from Sicily, the specimens recorded below are, I believe, the first
record for Algeria.
1 (J Blida les Glacieres, June 1908 (W. R. and K. J.) ; 1 J Sebdou, June 1918
(P. Rotrou).
[Parastichtis arabs biskrae (Oberth.).
Hadena arabs liskrae Oberthiir, Etiid. Lipid. Comp. fasc. xvi. p. 157 (1919) (Biskra).
I have no specimens of this pale sandy desert form.]
236. Eremobia alpigena (Boisd.).
Hadena alpigena Boisduval, Icon. Hist. Lipid. Tome ii. pi. 84. f. 5 (1834).
The series of this insect at Tring consists of 1 specimen from Digne (Victor
Cotte) and 26 from Algeria taken by ourselves.
26 Khenchela, May 1912 (W. R. and K. J.).
237. Eumichtis monochroma (Esp.).
Phalaena monochroma Espcr, Schmett. vol. iv. pt. ii. p. 521. No. 21G. pi. civ. ff. 3-6 (1791) (Florence).
Of this species the Mauretanian series at Tring consists of 47 specimens from
Environs de Batna May 1915, Lambessa October 1915 (A. Nelva coll.) ; Aflou,
October 1916 (V. Faroult) ; Ain Draham, September 1911 (V. Faroult) ; Sidi-
bel-Abbes, September 1917 (M. Rotrou) ; Guelt-es-Stel, October 1912-1913
(V. Faroult) ; El Mahouna, September 1919 (V. Faroult). Of these 20 are the
grey form and 26 the dark form, and 1 is ab. suberis.
60 NOVTTATES ZOOLOOICAE XXVII. 1920.
238. Eumichtis roboris cerris (Boisd.).
Hadena roboris var. cerris Boisduval, Ind. Meth. p. 121, sub No. 961 et footnote (1) (1840) (Spain,
S. France).
Mr. Oberthiir says that this insect is common at Lambessa in October and
November, and that Mr. Harold Powell took over 80 specimens ; I have only
3 Algerian specimens, and a specimen without locality out of the Sand collection.
1 <J Hammam Meskoutine, April 1914 (W. R. and K. J.) : 1 cJ, 1 ? Aflou,
October 1910 (V. Faroult).
239. Dryobota furva (Esp.).
Phalaena furva Esper, Schmetl. vol. iv. pt. ii. p. 530. pi. 158. ff. 1, 2 (1789) (Florence).
Here again Mr. Oberthiir states that this insect is very common, while I have
only received from Algeria 4 specimens. Mr. Oberthiir employs the name occlusa
for this species and gives as the author Esper. The name occlusa, however, was
given by Hiibner in 1827, 38 years subsequent to the date of Esper's furva, and
so the latter must be used.
3 (J(J, 1 ? Batna (A. Nelva coll.) ; 1 r? Guelt-es-Stel, October 191 3 (V. Faroult).
239a. Eumichtis accipitrina (Esp.).
Phalaena accipitrina Esper, Schmett. vol. iv. pt. ii. p. 393. pi. 129. f. 4 (1788) (Erlangen).
The series of this species at Tring consists of 56 Mauretanian specimens from
Aflou, October 1916 (V. Faroult) ; Lambessa and Batna, October 1911-1915 (A.
Nelva) ; Aflou October 1916, Guelt-es-Stel October— November 1913 (V. Faroult).
240. Eumichtis protea (Schiff. & Den.).
Phalaena protea Schiffermuller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 84 (1775) (Vienna).
Of this very variable insect I have 154 Algerian specimens from Environs de
Batna and Lambessa, October 1911-1915 (A. Nelva coll.) ; Aflou, October 1916
(V. Faroult) ; Guelt-es-Stel, October 1913 (V. Faroult).
241. Lophoterges millierei (Stdgr.).
Lithocampa millierei Staudinger, Berl. Entotn. Zeitschr. vol. xiv. p. 119 (1S70) (Catalonia).
I have only received 1 <$, 4 $$ of this very beautiful species.
1 $, 1 ?Sebdou July 1918, 1 $ Foret de Tenira August 1918 (P. Rotrou) ;
1 $ Hammam R'hira, May 1916 (V. Faroult) ; 1 ? El Mahouna, July 1919
(V. Faroult).
242. Dichonea areola mustapha (Oberth).
Xylorampa lithorhiza mustapha Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 164. pi. xdvi. f. 4124
(1919) (Lambessa).
Mr. Oberthiir uses for this species Borkhausen's name of lithorhiza. because
Guenee used it, but he acknowledges that it is the areola of Esper. As Esper's
name antedates Borkhausen's by 3 years, the species must stand as areola Esp.
We have at Tring 7 Mauretanian specimens from Alger, March 1914 (V.
Faroult) ; Blida February 1916, Hassi Baba November 1917, Hammam
R'hira February 1918, Lalla Marnia November 1914, Guelt-es-Stel October
1912 (V. Faroult).
Novitates Zoological XXVII. 1920. 61
243. Axylia exsoleta (Linn.).
Plialaena exsoleta Linnaeus, Syst. Nat. edit. x. p. 515. No. 104 (1758).
Almost all authors subsequent to Linnaeus spell the specific name of this
species exolela, but Linnaeus spells it exsoleta, both as regards the name he
bestows on the present insect and in the diagnosis ; he also spells it so in a
footnote. Now although the method of spelling the adjective exoletus is more
often used than the spelling exsoletus, both are correct Latin according to
standard dictionaries, and therefore as Linnaeus deliberately uses the spelling
with the s this must be adopted.
This insect appears to be rather uncommon in Mauretania. We have 6
specimens from Chauzy 1914 (M. Rotrou) ; Blida February 1916, Guelt-es-Stel
March— September 1913 (V. Faroult) ; 1 larva A'in Sefra, May 1913 (W. R. and
E. H.) ; 1 larva Hammam R'hira (V. Faroult); 1 $ Aflou, October 1916 (V.
Faroult).
244. Lithophane semibrunnea (Haw.).
Nociua semibrunnea Haworth, Lepid. Brit. p. 171 (1809).
The Algerian specimens I have are greyer than European ones. Mr. Oberthur
also mentions this, but states that Tunisian (Am Draham) specimens are very
red. As I have too few to judge, I refrain from naming it.
1 $ Batna October 1910, 1 £ Perregaux November 1915, 2 $$, 1 $ Hammam
R'hira February 1918 (V. Faroult).
245. Giapholitha lapidea ochreimacula (Rothsch.).
Cloantha ochreimacula Rothschild, Novit. Zool. vol. xxi. p. 329. No. 148 (1914) (Guelt-es-Stel).
It was unfortunate that I described this insect from the form with the
yellow reniform.
The Algerian subspecies differs from the European by being a duller purer
grey with the pattern more obliterated.
1 S Guelt-es-Stel, November 1913 (V. Faroult) ; 1 <J Batna, October 1910
(V. Faroult).
246. Cucullia verbasci (Linn.).
Plialaena verbasci Linnaeus, Syst. Nat. edit. x. p. 515. No. 105 (175S).
T never received this insect in any numbers, only 7 specimens coming to
hand in eleven years.
1 c?, 1 $ Hussein Dey, Alger, April 1910 (Captain Holl) ; 2 <$£ Batna, May
1915 (A. Nelva) ; 1 <J Hammam Meskoutine, April 1914 (W. R. and K. J.) ; 1 <J
Souk Ahras, 1 <$ Tebessa, April 1914 (W. R. and K. J.)
247. Cucullia thapsiphaga Treit.
Cucullia tlutpsipltarja Treitschke, Schmett. Eur. vol. v. pt. 3. p. 120. No. 16 (1826) (Styrian Frontier).
Of this species I only received 1 <J, 2 §§.
1 cJ, 1 $ Batna, May 1912 (A. Nelva coll.) ; 1 $ Hammam R'hira, May 1916
(V. Faroult).
62 Novitates Zoolooicae XXVII, 1920.
248. Cucullia scrophulariphaga Ramb.
Cucullia scrophulariphaga Rani bur, Ann. Soc. Entom. France, 1833, p. 20. pi. 1. f. 4 (Corsica).
Of this species I have also not received many.
5 cJcJ, 1 ? Environs de Batna, May 1912 (A. Nelva).
249. Cucullia oberthuri Rothsch. (PI. XVI. f. 6.)
Cucullia oberthuri Rothschild, Ann. Mag. Nat. Hist. (8) viii. p. 232. No. 3 (1911) (Bou Saada).
This is the insect Mr. Oberthur identified as anceps Stdgr. I have compared
it with anceps from various localities at Tring and in the British Museum, and Sir
G. Hampson agrees that it is a distinct species and not anceps (PI. XVI. f. 5).
The series now at Tring has been augmented by 3 specimens to 7 in all.
4 (JcJ Bou Saada April —May 1911, 1 (J El Kantara March— April 1911, 1 <J
Hammam R'hira April 1917 (V. Faroult) ; 1 $ Khenchela, May 1912 (W. R. and
K. J.).
250. Cucullia blattariae (Esp.).
Phalaena blattariae Esper. Schmett. vol. iv. pt. ii. p. 518. No. 214. pi. 154. f. 4 (1786) (Florence).
1 cj Plaines au Sud de Sebdou, May 1918 (P. Rotrou).
251. Cucullia scrophulariphila Stdgr.
Cucullia scrophulariphila Staudinger, Stett. Entom. Zeit. vol. xx. p. 215. No. 10 (1859) (Chiclana).
The ground-colour is more whitish in my Algerian specimens than in Spanish
ones, but this seems to be the case in all the Mauretanian C'ucullias of the verbasci
group. The Khenchela specimen is also much darker than the A'in Sefra ones.
1 <J Khenchela, June 1911 (V. Faroult) ; 2 (J;?, 1 $ A'in Sefra, March 1915
(V. Faroult).
251a. Cucullia biskrana 0 berth.
Cucullia biskrana Oberthur, Elud. Lipid. Comp. fasc. xvi. p. 167. pi. xdvi. ff. 4125, 4126 (1919)
(Biskra).
I have only received 1 J of this species.
1 o 20 kil. S. of Bledet Amar, December 1913 (Geyr von Schweppenburg).
252. Cucullia beata sp. nov. (PI. XVI. f. 7.)
jj. This I consider the handsomest species of the innbratica group.
Antennae brown, basal 10th white: head ash-grey: thorax pale bluish ash-
grey ; abdomen paler, more whitish ash-grey, slightly tinged with cream colour
laterally, median dorsal line and anal tuft darker.
Forewing pale bluish ash-grey, slightly freckled with brown-grey scales,
nervures in outer half darker, a median black line from base to halfway along
and below median nervure followed by a much heavier oblique black band at
the base of which is a cross bar. Above vein 4 is a narrow black line.
Hindwings semi-vitreous white, nervures and marginal band ash-grey.
Length of forewing, 17 mm. ; expanse, 39 mm.
1 <J Sebdou, September 1918 (P. Rotrou).
This species is nearly allied to ianiceti Schiff., but is much smaller, and the
black markings are very different.
Novitates Zoolooicae XXVII, 1920. 63
253. Cucullia chamomillae calendulae Trcit.
Cucullia chamomillae var. calendulae Treitschke, Schmett. Eur. vol. x. pt. 2. p. 127 (1835) (Sicily).
I have 61 Algerian specimens from Guelt-es-Stel, March — November 1912-
1913 (W. R. and K. J., and Faroult) ; Bou Saada, March— May 1911-1912 (V.
Faroult) ; Souk Ahras and Tebessa, April 1914 (W. R. and K. J.) ; Khenchela,
May 1912 (W. R. and K. J.) ; El Kantara, March— April 1911 (W. R. and E. H.,
and Faroult) ; Bordj Chegga, February 1912 (Hartert and Hilgert) ; Lalla
Marnia May 1914, Hammam R'hira February 1918 (V. Faroult) ; Berrou-
aghia, April 1914 (V. Faroult); Mazagan, Morocco, March — April 1902 (W.
Riggenbach). Among these are several fine examples of ab. amoenissima
Oberthur, Etud. Lepid. Comp. fasc. xvi. p. 169. pi. xdvi. f. 4129 (1919) (Biskra).
In the British Museum is 1 $ Morocco, January — February 1902, Meade
Waldo.
254. Cucullia santolinae Ramb.
Cucullia santolinae Rambur, Ann, Soc. Entom. France, vol. iii. p. 387. pi. 8. f. 4 (1834) (Corsica).
Of this species the series at Tring from Mauretania numbers 37 from Guelt-
es-Stel, March— April 1912-1913 (W. R. and K. J., and Faroult) ; Bou Saada,
May 1912 (V. Faroult); El Kantara March — April 1911, Boudj-ben-Aneridj
November 1911, Hammam R'hira February 1918 (V. Faroult); Batna (Nelva
coll.) ; Khenchela May 1912, Hammam Meskoutine April 1914 (W. R. and
K. J.) ; Environs d' Alger and Hussein Dey, January — December 1908-1911
(W. R. and E. H, and Captain Holl) ; Mazagan, Morocco, February 1902 (W.
Riggenbach). One of the 2 specimens from Hammam Meskoutine was bred from
a larva found April 1914 and emerged at Tring March 1915.
255. Copicucullia syrtana (Mab.).
Cucullia sijrlana Mabille, Bull. Soc. Entom. France, 1888, p. 51 (Gab&s).
Of this species the Tring series consists of 85 specimens from Colomb-Bechar
February— March 1912, Bir Stil March 1917, El Kantara March— April 1911,
Bordj Chegga March 1917, Ai'n Draham September 1911 (V. Faroult) ; Bordj
Chegga, Bordj Saada, Nca-ben Rzig, February 1912 (Hartert and Hilgert) ;
Ghardala, April 1911 (W. R. and E. H.) ; Arefidji, March 1912 (Hartert and
Hilgert) ; Biskra, March 1909 (W. R. and E. H.); Oued Abou, January 1914
(Geyr von Schweppenburg).
In British Museum 3 $,$, 5 $$ Hammam-es-Salahin, January — March 1904,
Lord Walsingham.
256. Empusada argentina (Fabr.).
Noctua argentina Fabricius, Mant. Ins. vol. ii. p. 162. No. 185 (1787) (South Russia).
The Tring series from Mauretania consists of 50 specimens from A'in Sefra,
May 1913 (W. R. and E. H.) ; Mecheria, May 1918 (V. Faroult) ; Batna (A.
Nelva and Faroult) ; Bou Saada, May 1912 (V. Faroult) ; Tilghemt, April 1911-
1912 (W. R. and E. H., and V. Faroult) ; Khenchela, May 1912 (W. R. and K. J.) ;
Les Pins August 1918, Environs de Taourirt September 1918 (M. Rotrou).
g4 NOVITATES ZOOLOGICAE XXVII. 1920.
257. Brachygalea albolineata (Blach.).
Oolophasia albolineata Blachier, Bull. Soc. Entom. France, 1905. p. 53 (Gafsa).
Mr. Warren was perfectly correct in Seitz, when he said that Brachygalea
leucorliabda and Criophasia albolineata Hampson are one and the same. As the
Zoological Record only comes out more than a year later than the one recorded,
it is not astonishing that Sir George Hampson missed Mr. Blachier's article ;
but it is certainly an unfortunate slip, that he did not notice that his leucorhabda
was the same as the insect he received from Bang-Haas under the name albolineata.
As leucorliabda is designed as the type of Brachygalea and albolineata as that of
Criophasia and Brachygalea has 114 pages priority over Criophasia, it is quite
evident that Brachygalea must stand as the genus-name.
Our series at Tring from Mauretania numbers 167 specimens from Biskra,
February— March 1908-1914 (W. R. and E. H.) ; Bir Djefair, March 1909 (W. R.
and E. H.) ; Ain Sefra, March— May 1913-1915 (W. R. and E. H., and Faroult) ;
Guelt-es-Stel April— May 1913, Bou Saada March 1912, El Kantara March-
April 1912 (V. Faroult); Bordj Chegga, February — March 1912-1917 (Hartert
and Hilgert, and Faroult) ; Kef-el-Dohr, Mraier February, Arefidji, north of
Ouargla March 1912, Oued Nca April 1914 (Hartert and Hilgert).
In the British Museum are 1 <$ Tunis ; 3 <$$, 1 $ Hammam-es-Salahin, April
1904, Lord Walsingham.
258. Hypomecia quadrivirgula (Mab.).
Epimecia quadrivirgula Mabille, Bull. Soc. Enlom. France, 1888, p. 51 (Gabes).
Our series at Tring of this species consists of 138 specimens from Guelt-es-
Stel, October— November 1912-1913 (V. Faroult); Alger January 1914, Bou
Saada March 1912, El Mesrane November 1913, Hassi Baba November 1917
(V. Faroult).
259. Rabinopteryx subtilis (Mab.).
Epimecia subtilis Mabille, Bull. Soc. Enlom. France, 1888, p. 51 (Gabes).
Mabille was almost right in placing this insect in Epimecia, as it is next to
that genus, differing in the upturned instead of porrect palpi.
Our Tring series numbers 258 from Guelt-es-Stel March — May 1913, Bou
Saada April 1911, Berrouaghia April 1914, Mecheria May 1918 (V. Faroult);
Bordj Chegga, February— March 1912-1917 (Hartert and Hilgert, and Faroult) ;
Biskra, March— April 1908-1914 (W. R. and E. H.) ; Ain Sefra, March— May
1913-1915 (W. R. and E. H., and Faroult).
The British Museum has 1 <J, 4 $$> Hammam-es-Salahin, March — April 1904,
Lord Walsingham.
260. Rabinopteryx <nelvai sp. nov. (PI. XVI. f. 4.)
$. Antennae brown ; head and thorax brown-grey variegated and irrorated
with dark brown ; abdomen yellowish pale grey.
Forewing brown-grey, densely striolated with dark brown ; 3 oblique bars
on middle of costal area and the orbicular and reniform brown, a somewhat
obscured white band below median vein from base almost to termen, beneath
NOVITATES ZOOT.OGICAE XXVII. 1920. 65
which and coalescing with it is a similar black-brown band. Hindwings creamy
grey, somewhat suffused with brownish grey.
Length of forewing, 13 mm. ; expanse, 28 mm.
1 $ Batna, 1914 (A. Nelva coll.).
261. Catamecia mauretanica Stdgr.
Catamecia jordana var. mauretanica Staudinger, Cat. Lepid. Palaear. Faun. pt. i. p. 213. No. 2192ft
(1901) (Biskra).
Mr. Oberthiir, agreeing with Mr. Culot and Staudinger, places this insect
as a subspecies of jordana Stdgr., but after examining it with Sir George Hampson
I have come to the conclusion that it is a distinct species, both from jordana
Stdgr. and minima Swinh. (=bacheri Stdgr.). It differs from both in the white
claviform patch edged with black.
1 have 15 specimens.
2 Biskra, March 1909-1911 (W. R. and E. H.) ; 12 Bordj Chegga, 1 Bir Stil,
March 1917 (V. Faroult).
The British Museum has 1 $ Tkout, April 1906, 3 $$, 3 ?$ Hammam-es-
Salahin, April 1904, Lord Walsingham.
[Catamecia jordana balestrei D. Lucas.
Catamecia jordana var. balestrei Daniel Lucas, Bull. Soc. Entom. France, 1907, p. 181 (Nefta).
I have never received this species.]
262. Omia cyclopea (Grasl.).
Cleopliana cyclopea Graslin, Ann. Soc. Entom. France, vol. v. 570. pi. 17 B. f. 7 (1836) (Alfakar,
Grenada).
All the Omias are extremely rare.
1 c?, 1 ? Lambessa (Staudinger) ; 1 $ Algeria (Deyrolle) ; 1 $ El Kantara,
May 1909 (W. R. and E. H.).
263. Omia oberthuri Allard.
Omia oberthuri Gaston Allard, Ann. Soc. Entom. France, vol. sxxvi (aer. iv. vol. 3). p. 320. pi. 6.
ff. 3a, 36 (1807) (Lambessa).
1 (J, 1 ? Lambessa (Staudinger).
264. Amephana warionis (Oberth.).
Cleophana warionis Oberthiir, Elud. Entom. livr. i. p. 48. pi. 2. f. 3 (1876) (Bou Saada).
Our series at Tring contains 185 specimens from Ain Sefra, May 1913 (W. R.
and E. H.) ; Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and Faroult) ;
Bou Saada March — April 1912, El Outaya March, El Mantara March — April
1911 (Victor Faroult) ; Biskra, Gafsa, Tunis (Staudinger) ; Tilghemt, April 1911-
1912 (W. R. and E. H., and Faroult) ; Mecheria, Djebel Antar, May 1918 (V.
Faroult) ; Sebdou, May 1918 (P. Rotrou).
In the British Museum are 2 $$ Tunis, Staudinger and Bang-Haas.
5
66 Novitates Zoolooicae XXVII. 1920.
265. Cleophana boetica diluta Rothsch. (PL XV. ff. 16, 17 [18].)
Cleophana boeiica diluta Rothschild, Ann. Hag. Sat. Hist. (8) viii. p. 232 (1911) (Bou Saada).
Mr. Oberthiir as usual ignores my name, because unaccompanied by a figure ;
but acknowledges himself that the Algerian form is paler than the two European
races.
Our series at Tring contains 409 specimens from Lalla Marnia May 1914,
Bou Saada March — April 1912, Berrouaghia April 1914, Masser Mines May
1914, Mecheria May 1918 (V. Faroult) ; Khenchela, May 1912, Souk Ahras
April, Tebessa April 1914 (W. R. and K. J.); Batna, May 1915 (A. Nelva) ;
Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and Faroult); Sebdou,
May 1918 (P. Rotrou) ; Sidi-bel-Abbes, May 1918 (M. Rotrou).
In British Museum 1 (J Bou Saada ex Tring Museum.
265a. Amephana warionis x CI. boetica diluta. (PL XV. f. 19.)
This specimen, taken at Guelt-es-Stel by Victor Faroult, April 8th, 1913,
appears to me undoubtedly a hybrid between the above two species. It is some-
what intermediate in pattern, and while the general facies and colour are that
of boetica diluta it is strongly suffused with green.
266. Omphalophana serrata (Treit.).
Cleophana serrata Treitschke, Schmett. Eur. (Suppl.) vol. x. pt. 2. p. 121 (1835) (Sicily).
This species is rather rare in Mauretania.
We have from Mauretania 100 specimens at Tring from Mazagan, Morocco,
April 1902 (W. Riggenbach) ; Morocco (Staudinger) ; Moroccan Frontier S.W. of
Lalla Marnia May 1914, Lalla Marnia May 1914 (V. Faroult); Environs d'Alger
May 1908, Hammam Meskoutine April, Souk Ahras April 1914, Khenchela
May 1912 (W. R. and K. J.); Am Draham and Djerba, Tunisia (Staudinger,
Bartels, and Dannehl) ; Sidi Ferruch, April 1911 (Andre Thery) ; Hammam
R'hira, May 1908-1917 (W. R., E. PL, and K. J., and Faroult) ; Batna, May 1915
(A. Nelva) ; El Mahouna, May— June 1919 (V. Faroult).
267. Cleophana jubata Oberth.
Cleophana jubata Oberthiir, Etud. Entom. livr. xiii. p. 31. pi. 6. f. 40 (1890) (Gabes).
This is a rare species.
The Tring series contains 71 specimens from A'in Sefra, May 1913 (W. R.
and E. H.) ; Mecheria May 1918, Bou Saada April — May 1912 (V. Faroult) ;
Tilghemt, April 1911 (VV. R. and E. H.) ; Guelt-es-Stel, April— May 1912-1913
(W. R. and K. J., and Faroult) ; Sebdou, May 1918 (P. Rotrou).
In the British Museum are 1 (J, 1 $ Tunis, Staudinger and Bang-Haas.
268. Omphalophana pauli (Stdgr.).
Cleophana pauli Staudinger, Iris, vol. iv. p. 30. pi. 4. f. 4 (1891) (Jerusalem).
Of this species there are 74 Mauretanian specimens at Tring from Lalla
Marnia April 1914, Mecheria May 1918, Berrouaghia April 1914, Guelt-es-Stel
NOV1TATES ZOOLOGICAE XXVII. 1920. 67
April— May 1913, Bou Saada March— April 1912 (V. Faroult) ; Tunis (Stau-
dinger) ; Ain Sefra, May 1913 (W. R. and E. H.).
In the British Museum 1 $ Tunis, Staudinger and Bang-Haas.
269. Cleophana pectinicornis Stdgr.
Cleophana pectinicornis Staudinger, Stett. Entom. Zeil. vol. xx. p. 215. No. 9 (1859) (Chiclana).
This fine species is abundant in some localities in Algeria.
The Mauretanian series at Tring numbers 454 specimens from Lalla Marnia
May 1914, Bou Saada March— April 1912, El Kantara March— April 1911 (V.
Faroult); Fontaine Chaude, April 1909 (W. R. and E. H.) ; Gafsa, Tunisia
(Staudinger) ; Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and
Faroult) ; Sebdou, April 1918 (P. Rotrou).
Mr. Oberthiii' states that the typical Spanish form of this insect differs from
Mauretanian examples in the brown being duller and darker. I have never seen
Spanish specimens, but Rambur's figure (Cat. Syst. Ins. de VAndal. pi. xii. f. 4)
only shows the fringe of the forewings less yellow, otherwise it agrees exactly.
In the British Museum 1 <J Tunis.
270. Copiphana gafsana (Blach.).
Cleophana gafsana Blachier, Bull. Soc. Entom. France, 1905. p. 53 (Gafsa).
Mr. Oberthiir quite rightly points out that Cleophana albino, B.-H. is
nothing but an albinistic gafsana Blach. and rightly says it is intermediate between
Mr. Culot's figures 14 and 15, pi. 59. I propose for Mr. Culot's figure 14 the
name of ab. intermedia ab. nov., so that there would be 3 named aberrations of
yafsana, viz. (1) ab. intermedia Rothsch., pattern of wings fully developed, though
much paler than typical form, on a pale ground-colour ; (2) ab. albina B.-H.,
ground-colour pure white, pattern partially obliterated ; (3) ab. blachieri Oberth.,
entirely white nervures showing darker.
This insect appears to be much more confined to the desert regions.
We have at Tring 62 specimens from Colomb-Bechar March — -April 1912,
Bou Saada April 1911 (V. Faroult) ; Tilghemt, April 1911-1912 (W. R. and E. H.,
and Faroult) ; Gharda'ia, April 1911 (W. R. and E. H.) ; Tunis (Staudinger) ;
Bir Djefair, March 1909 ( W. R. and E. H.) ; Oued Nca April 1914, N. of El Golea
March, Mraier March 1912 (Hartert and Hilgert).
In the British Museum 1 J, 1 $ Tunis.
271. Cleophana vaulogeri Stdgr.
Cleophana vattlogeri Staudinger, Iris, vol. xii. p. 378. pi. 5. f. 9 (1899) (Biskra).
Mr. Oberthiir says this is very common ; I have only had few specimens
compared to the numbers of some other species of this group.
The Mauretanian series at Tring consists of 80 specimens from El Outaya
March 1911, El Kantara March 1911, Ain Draham September 1911, Colomb
Bechar March — April 1912, Bou Saada, Laghouat March — April 1912, Tilghemt
April 1912 (V. Faroult) ; Ain Sefra May 1913, Biskra March— April 1908-1914
(W. R. and E. H.) ; Oued Nca, April 1914 (Hartert and Hilgert).
In the British Museum are 3 rftf, 3 $$ Hammam-es-Salahin, April 1904, Lord
Walsingham.
68 Novitates ZOOLOOI0A.E XXVII. 1920.
272. Cleophana fatinia B.-H. (PI. XV. ff. 13-15.)
OUophana fatima Bang-Haas, Iris, vol. xx. p. 73. p. 3. f. 14 (1907) (Tunis, Gafsa, etc.).
Both Herr Bang-Haas and Mr. Oberthiir have mixed up two species under
the name fatima — Herr Bang-Haas when sending out specimens to clients and
Mr. Oberthiir when figuring the species (Etud. Lipid. Camp. fasc. v. pt. i.) ; in
fact Mr. Oberthiir has mixed more than two species, as his figure 599 agrees well
with versicolor Stdgr.
The diflluem-vaulogeri group are very difficult to unravel, but I am con-
vinced that Staudinger and Hampson have treated too many good species as
varieties of diffluens and its European relations. I shall figure these to show the
differences more clearly to Mr. Oberthiir and his friends, who will not acknow-
ledge any other method of identification.
I have only 4 specimens of this species, which appears to be essentially
Tunisian and very rare in Algeria. 1 specimen each from Gafsa, Tunisia
(Staudinger) (co-type) ; Tilghemt, April 1912 (V. Faroult) ; Ghardaia, April
1911 (W. R. and E. H.) ; Oued Xca, April 1914 (Hartert and Hilgert).
In the British Museum 1 $ Tunis, Staudinger and Bang-Haas.
273. Cleophana affinis sp. nov. (PI. XV. f. 6.)
Differs from fatima at first sight by its larger size and bright rufous not
yellowish grey ground-colour.
This is the insect figured by Mr. Oberthiir (Etud. Lipid. Gomp. fasc. v. pt. i.
ff. 596, 597, 598) as fatima Bang-Haas ; but which is not that species. This
mistake probably arose through Mr. Oberthiir having received from Dresden
some of the later specimens sent out by Bang-Haas as fatima, but if not, then it
is much more easily accounted for, because the photographic figure of fatima
in the Iris would be easily confounded with the present species.
cj $. Head and thorax deep rufous, not cream-white as in fatima, variegated
grey and dark brown edgings ; abdomen wood-brown not yellowish grey.
Forewing rufous, not bluish grey washed with buff as in fatima ; the fringe
is rufous and brown, not dark wood-grey and buff ; the postmedian line is much
more deeply angled, especially at vein 5 ; the lunate mark in the centre of the
reniform is rufous, not black as in fatima. Hindwing basal half yellowish wood-
grey, not cream- white as in fatima. (Type ? Mecheria.)
Length of forewing, fatima $, 10 mm. ; expanse, 24 mm.
Length of forewing, affinis ?, 14 mm. ; expanse, 33 mm.
16 specimens from Bou Saada May 1911, Guelt-es-Stel April, Bou Sedraia
X. of Djelfa May 1913, Mecheria May 1918 (V. Faroult) ; Ain Sefra, May 1913
(W. R. and E. H.) ; Sebdou, May 1918 (P. Rotrou).
274. Cleophana chabordis Oberth.
Cleophana chabordis Oberthiir, Elud. Entom. livr. i. p. 47. pi. ii. f. 2 (1876) (Bou Saada).
This in the more southern and desert regions appears to be very common.
The series at Tring numbers 543 specimens. Mr. Oberthiir, because the white
variety named albicans Stdgr. was not figured, calls this albino aberration niveata.
Although aberrations are not supposed to be subject to the law of priority, still
Staudinger's name, having been given fourteen years earlier, ought, I think, to
NOVITATES ZOOLOGICAE XXVII. 1920. 69
be used. The numerous specimens intermediate between the ab. albicans and
normal chabordis I propose to call ab. semialbicans ab. nov.
Our 547 examples are from El Kantara March — April 1911, Tilghemt April
1912, El Hamel May 1912, Bou Saada March— April, Djebel Kerdada May 1912,
Guelt-es-Stel April 1913, Colomb-Bechar March — April 1912, Bordj Chegga March,
Bir Stil March 1917 (V. Faroult) ; Biskra March— April 1908-1914, Mraier
April 1909 (W. R. and E. H.) ; Laghouat, March— April 1911-1912 (W. R. and
E. H., and Faroult) ; Ain Sefra, May— July 1913-1915 (W. R. and E. H., and
Faroult) ; Dehibat, Ain Draham, and Gafsa, Tunisia (Staudinger) ; South Oued
Mya halfway between Ouargla and Touggourt, El Alia between Touggourt and
Guerrara, Guerrara, Hassi Sidi Mahmud March — April 1912, Oued Nca April
1914 (Hartert and Hilgert) ; Oued Amrah, April 1914 (Geyr von Schweppenburg).
Of the 547 specimens 102 are ab. semialbicans and 42 ab. albicans.
In the British Museum are 3 (J^, 3 $$ Hammam-es-Salahin, March — April
1 904, Lord Walsingham ; 1 <J ab. albicans, Tunis.
275. Amephana anrita (Fabr.).
Noctua aurila Fabrioius, Mant. Ins. vol. ii. p. 179. No. 282 (17S7) (Spain).
The series at Tring from Mauritania consists of 512 examples from Moroccan
Frontier S.W. of Lalla Marnia May 1914, Lalla Marnia May 1914, Berrouaghia
April 1914, Bou Saada May 1914 (V. Faroult) ; Batna, May 1911-1915 (A. Nelva) ;
Hammam Meskoutine April — May 1914, Tebessa and Sunk Ahras, April 1914
(W. R. and K. J.); Khenchela, May— June 1911-1912 (W. R. and K. J., and
Faroult) ; Environs d'Alger, April— May 1908 (W. R., E. H., and K. J., and Dr.
Nissen) ; Sidi Ferruch, April 1914 (A. Thery) ; Les Pins, June 1918 (M. Rotrou) ;
Hammam R'hira, May 1908-1917 (W. R. and K. J., and Faroult) ; Gabes, Tunisia
(Staudinger); Guelt-es-Stel, April— May 1912-1913 (W. R. and K. J., and
Faroult) ; Sebdou, Foret de Tenira, May 1918 (P. Rotrou); El Mahouna, June
1919 (V. Faroult).
Mr. Oberthiir employs for this species the name of dejeanii Dup., as aurita
Fabr. is not accompanied by a figure ; but aurita has forty years' priority over
dejeanii.
276. Cleophana diffluens mauretaniae subsp. nov. (PI. XV. f. 11.)
<J ?. Differs from diffluens diffluens Stdgr. in having no shade of red-brown
whatever ; d. mauretaniae differs from diffluens lusitanica Culot in having the
distal half of the forewings sharply divided from the basal half, the basal half
being almost deep black while the distal half has the ground-colour brown-grey.
In this it is much nearer d. diffluens, as d. lusitanica has the distal half of the
forewings sooty, so that in many specimens there is hardly any difference of
ground-colour of the whole forewing.
This is the insect Mr. Oberthiir enumerates as diffluens diffluens from Tunisia.
This is the first record for Algeria.
I have at Tring of this new form 25 specimens from Hammam Meskoutine,
May 1914 (W. R. and K. J.) ; El Mahouna, May 1919 (V. Faroult).
I have compared this with Chiclana specimens of d. diffluens (PI. XV. f. 10),
and a series of 113 d. lusitanica collected by Dr. Jordan at Monchique in Portugal.
70 Novitates Zoolooicae XXVII. 1920.
[Cleophana difBuens lusitanica Culot. (PI. XV. f. 12.)
Cleophana diffluent form, lusitanica Culot, Noct. et Gkom. d'Eur. pt. i. vol. ii. p. 107. pi. 59. f. 10
(1915) (South Portugal).
Differs from diffluens diffluens and d. mauretaniae in having the whole fore-
wing black, the basal half only in some specimens being of a deeper black.
This form was distributed by Staudinger and Bang-Haas under the name
of lusitanica, but I find the name was not published, so Mr. Culot's figure and
description of ground-colour prove to be the first publication and he stands as
the author.]
277. Cleophana versicolor Stdgr. (PI. XV. ff. 7, 8.)
Cleophana diffluens ab. versicolor Staudinger, Cat. Lipid. Pal. Faun. pt. i. p. 214. No. 221Ga (1901)
(Mauretania).
Mr. Culot and Sir George Hampson have also treated this as an aberration
of diffluens, while Mr. Oberthiir calmly ignores it altogether. It is, however, a
perfectly distinct species and occurs together with diffluens mauretaniae.
We have at Tring 30 specimens from Constantino (Staudinger) ; Am Draham
September 1911, Hammam R'hira May 1917, Bou Saada March — April 1912,
Guelt-es-Stel April 1913, Mecheria May 1918 (V. Faroult) ; Ai'n Sefra, May 1913
(W. R. and E. H.) ; Sebdou, May 1918 (P. Rotrou).
278. Cleophana marocana Stdgr. (PI. XV. f. 9.)
Cleophana diffluens var. marocana Staudinger, Cat. Lipid. Pal. Faun. pt. i. p. 214. No. 22166 (1901)
(Morocco).
Mr. Oberthiir is somewhat doubtful as to the status of this insect, but I am
convinced it is a good and distinct species.
There are 12 specimens at Tring : 4 Tangier (Staudinger) ; 1 Rabat (A.
Thery) ; 7 Sebdou, Morocco (A. Thery).
The British Museum has 3 <$<$ Forest of Marmora, March 1903, Meade- Waldo.
[Omphalophana adamantina (Blach.).
Calophasia adamantina Blachier, Bull. Soc. Entom. France, 1905, p. 214 (Rabat).
I cannot understand how all the authors, except the late William Warren,
who mention this species have placed it in the genus Calophasia. Except for
its black hindwings it is almost identical with pauli Stdgr., in fact Mr. Meade-
Waldo (Trans. Entom. Soc. Lond. 1905) described and figured the specimen now
in the British Museum as Cleophana pauli Stdgr.
I have not received this species.
The British Museum has 1 $ Forest of Marmora, April 1903, Meade- Waldo.]
279. Calophasia kraussi Rebel.
Calophasia kraussi Rebel, Verh. Zool. Bot. Ges. Wien, 1895 p. 34S (Oued Nouemra, Sahara).
Mr. Culot (Noct. et Geom. d'Eur. pt. i. vol. ii. p. 101. pi. 58. f. 6) describes
and figures the white aberration of kraussi as form, nmozim ; but already in 1913
(Novit. Zool. vol. xx. pp. 124-125) I have described two aberrations of this
species, the second ab. albo-ochracea being very close to Mr. Culot's maozim.
.NOVITATES ZOOLOOICAE XXVII. 1920. 71
There are therefore three described aberrations : ab. maozim Culot, almost pure
white ; ab. albo-ochracea Rothsch., white with buff lines ; ab. brunnea Rothach.,
like the typical form, but whole wings suffused and saturated with brown. I
further propose to name the specimens intermediate between kraussi and ab.
albo-ochracea ab. intermedia ab. nov.
The series at Tring consists of 118 examples from Colomb-Bechar March —
April 1912, Bou Saada March 1912, Laghouat March 1912, A'in Draham Sep-
tember 1911, Guelt-es-Stel April 1913 (V. Faroult) ; Tilghemt April, Ghardaia
April 1911 (W. R. and E. H.) ; halfway between Touggourt and Ouargla, Arefidji
north of Ouargla, Hassi-el-Hadjar, halfway between Ouargla and El Golea, north
of El Golea, South Oued Mya, March— May 1912 (Hartert and Hilgert).
Of these 118 specimens there are 2 ab. maozim, 3 ab. brunnea, 12 ab. albo-
ochracea, and 27 ab. intermedia, leaving 74 typical kraussi.
The British Museum has 1 $ Hammam-es-Salahin, April 1904, Lord
Walsingham.
280. Calophasia platyptera (Esp.)
Noctua platyptera Esper, Schmett. vol. iv. pt. 2. p. 396. No. 138. pi. 130. f. 5. (1788) (Frankfort).
The proportion of albinistic specimens in this species is very large.
Our series at Tring numbers 26 specimens, of which 20 are albinistic = ab.
subalbida Stdgr.
26 examples from Ai'n Draham, August 1911 (Faroult and Staudinger) ; Souk
Ahras, April 1914 (W. R. and K. J.) ; Hammam R'hira, April— May 1912-1917
(W. R. and K. J., and Faroult) ; Tizi Ouzou August 1914, north side of Djebel
Zaccar August 1916 (Faroult) ; Environs d'Alger (Captain Holl).
281. Calophasia almoravida Grasl.
Calophasia almoravida Graslin, Ann. Soc. Bntom. France, 1863. p. 319. pi. 8. f. 6 (Grenada).
Of this species I have 10 Algerian examples from Guelt-es-Stel April 1913,
Bou Saada April 1912 (V. Faroult) ; Hammam Meskoutine April 1914, Khenchela
May 1912 (W. R, and K. J.).
282. Calophasia stigmatica Rothsch. (PI. XV. f. 26.)
Calophasia stigmatica Rothschild, Novit. Zool. vol. xx. p. 125. No. 49 (1913) (halfway between
Ouargla and El Golea).
So far I have only received three specimens of this rare species ; Herr Piingler
of Aachen has two others from Biskra.
1 £ South Oued Mya April, 1 $ halfway between Ouargla and El Golea
March 1912 (Hartert and Hilgert) ; 1 $ Guelt-es-Stel, April 1913 (V. Faroult).
283. Metapistis picturata (Rothsch.). (PI. XVI. ff. 2, 3.)
Cleophana picturata Rothschild, Entom. Zeilschr. vol. xxii. p. 142 (1909) (Mraier).
When Sir George Hampson first examined the single type specimen, he
considered it belonged to the genus Harpagophana, but on my procuring three
further specimens a thorough re-examination proved that this pretty little species
was not a Cucullid at all, but must be placed in the Noctuinae under the genus
Metapistis. Herr Bang-Haas of Dresden has received from Tunisia a fifth
specimen.
72 NOVITATES ZOOLOG1CAE XXVII. 1920,
4 $? from Oued Nca April 1914, Arefidji north of Ouargla March 1912
(Hartert and Hilgert) ; AIn Sefra, May 1915 (V. Faroult).; Mraier, April 1909
(W. R. and E. H.).
284. Rhodocleptria incarnata (Frej'er).
Noctua incarnata Freyer, Xeu. Beilr. Schmett. vol. iii. p. 91. pi. 256. f. 4 (1839) (Constantinople).
64 Mauretanian specimens of this species are at Tring from Environs d'Alger,
May 1908 (W. R. and K. J.) ; Bou Saada, May 1910-1911 (V. Faroult) ; Souk
Ahras, April 1914 (VV. R. and K. J.) ; Guelt-es-Stel, April— May 1912-1913 (W. R.
and K. J., and Faroult).
285. Xylina delphinii darollesi (Oberth.).
Chariclea darollesi Oberthiir, Etud. Entom. livr. i. p. 49. pi. 4. £. 5 (1S76) (El Hacalba).
This insect appears to be rare in Algeria, as I have only received 5 specimens.
2 Bou Saada May 1911 (V. Faroult); 2 Foret de Tenira, 1 Sebdou June
1918 (P. Rotrou).
286. Chloridea nubigera (H.-Sch.).
Heliothis nuliigera Herrich-Schaflier, Syst. Bearb. Schmett. Eur. p. 366 (1845) (Asia Minor).
The Mauretanian series at Tring consists of 155 specimens from Biskra
March 1908, Col de Sfa (bred) (W. R. and E. H.) ; Khenchela June 1911, Bou
Saada May 1911, Lalla Marnia May 1914, El Kantara August 1917, Mecheria
May 1918, Djebel Antar May 1918 (V. Faroult) ; Oued Nca April 1914, Ghardaia
May 1914, north of Am Guettera April 1912 (Hartert and Hilgert) ; Sidi-bel-
Abbes, May 1916-1917 (M. Rotrou) ; Sebdou, July 1918 (P. Rotrou) ; Am Sefra,
May 1913-1915 (W. R. and E. H., and Faroult) ; Saida, May 1913 (W. R. and
E. H.) ; Environs d'Alger (Captain Holl) ; Guelt-es-Stel, May 1913 (V. Faroult) ;
Oueds Amra, Dehin, Ag-elil, March 1914 (Geyr von Schweppenburg) ; Les Pins,
Titen Yaya May — August 1915 (M. Rotrou).
The British Museum has 1 ? Algeria, Mrs. Nicholl.
287. Chloridea peltigera (Schiff. and Den.).
Phalaena peltigera Schifferniuller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 89 (1775)
(Vienna).
Of this world-wide species, the series at Tring from Mauretania comprises
285 specimens from Hammam Meskoutine, May 1909-1914 (VV. R., E. H., and
K. J.); El Kantara, June— August 1909-1917 (Sidi Brahim and V. Faroult);
Khenchela June 1911, Bou Saada May 1911, Perregaux September 1915, Masser
Mines June 1914, Lalla Marnia May 1914, Moroccan Frontier May 1914, Mecheria
and Djebel Antar June 1918, A'in Sefra May 1915, Djelfa June 1913, AIn Draham
August 1911 (V. Faroult) ; Titen Yaya May 1915, Sidi-bel-Abbes June — Septem-
ber 1917 (M. Rotrou) ; Biskra, March 1908 (W. R. and E. H.), Hammam R'hira,
May — June 1908-1916 (W. R., E. H., and K. J., and Faroult) ; Mazagan, Morocco
June 1901, Rio de Oro, south of Morocco August 1902 (W. Riggenbach) ; Guelt-
es-Stel, March— October 1912-1913 (W. R. and K. J., and Faroult) ; Environs
de Taourirt, Morocco, July 1918 (M. Rotrou); El xMahouna, June 1919 (V.
Faroult).
In the British Museum are 1 cJ, 1 $ Algeria, Mrs. Nicholl.
NoVITATES ZOOLOGICAE XXVII. 1920. 73
288. Chloridea obsoleta (Fabr.).
Noctua obsoleta Fabricius, Entom. Syst. vol. iii. pt. i. p. 456. No. 155 (1793) (South American Islands).
I have very few Algerian specimens of this widespread species.
15 specimens from Mazagan, Morocco, July 1903 (W. Riggenbach) ; Sidi-bel-
Abbes, June— July 1917-1918 (M. Rotrou).
289. Melicleptria scutosa (Schiff. and Den.).
Phalaena scutosa Schiffermuller and Denis, An!:. Syst. Werk. Schmett. Wienergeg. p. 89 (1775) (Vienna).
Of this very widespread insect the Mauretanian material at Tring consists
of 158 examples from Bou Saada April — May 1911-1912, Djebel Kerdada May
1912, Puits Baba May 1913, Guelt-es-Stel April— October 1913 (V. Faroult) ;
Guelt-es-Stel, April 1912 (W. R. and K. J.).
290. Chloridea dipsacea (Linn.).
Phaiatna dipsacea Linnaeus, Syst. Nat. edit. xii. p. 856. No. 185 (1767) (Sweden).
This insect appears to be rare in Mauretania. I have only 9 specimens from
Djebel Mekter, Ain Sefra May 1913 (W. R. and E. H.) ; Batna (Nelva coll.) ;
Khenchela, May 1912 (W. R. and K. J.) ; El Misab, June 1918 (P. Rotrou).
The British Museum has 1 $ Forest of Marmora, Morocco, Meade-Waldo.
[Erithrophaia canroberti Oberth.
JSrythrophaia canroberti Oberthiir, Elud. Lipid. Comp. fasc. xvi. p. 182. pi. xdvii. f. 4130 (1919)
(El Outaya).
This species must be extraordinarily rare, as only the single (J? in Mr.
Oberthur's collection are known.]
291. Heliothis chanzyi (Oberth.).
Anihotcia chanzyi Oberthiir, Elud. Entom. livr. i. p. 51. pi. 2. ff. 4a, b. (1876) (Oued Djeddi).
I have only a single $ of this species taken by ourselves.
1 ? Guelt-es-Stel, April 1912 (W. R. and K. J.).
292. Xanthodes malvae (Esp.).
Noctua malvae Esper, Schmett. vol. iv. pt. 2. sect. 2. p. 63. No. 241 (1796) (Hungary).
I have only received 12 Algerian specimens of this species. 2 (JcJ Environs
d' Alger (Captain Holl) ; 1 $ Biskra, April 1909 (W. R. and E. H.) ; 2 $$, 1 $ El
Kantara August 1917, 1 $ Perregaux October 1915 (V. Faroult) ; 3$$ Sidi-bel-
Abbes, August — September 1917 (M. Rotrou) ; 2 $$ Foret de Tenira, July 1918
(P. Rotrou).
293. Aegle vespertalis (Hiibn.).
Pyralis vespertalis Hubner, Samml. Eur. Schmett. Pyr. f. 159 (1818).
Of this species there are at Tring 179 Mauretanian specimens from Guelt-es-
Stel May — June 1913, Lalla Marnia May 1914, Sakamodi August 1912, Nedroma
May 1914, Moroccan Frontier May 1914, Zoudj-el-Beghal July 1914, Masser
74 NOVTTATES ZOOLOGICAE XXVII. 1920.
Mines May 1914, Ain Draham August 1911, Khenchela June 1911, north side of
Djebel Zaccar August 1916, El Mesrane June 1913 (V. Faroult) ; Sidi-bel-Abbes,
June— August 1916-1918 (M. Rotrou) ; Hammam R'hira, May 1913 (W. R. and
E. H.) ; Hammam Meskoutine, May 1909-1914 (W. R., E. H., and K. J.) ; Sebdou,
Foret de Tenira, June 1918 (P. Rotrou).
Some of these specimens have lost all the brown transverse bands of the
fore- and hindwings, and look exactly like Metaegle pallida Stdgr., which caused
me to record this latter from Guelt-es-Stel.
[Erastria trabealis trabealis (Scop.).
Phalaena trabealis Scopoli, Entom. Carn. p. 240 (1763) (Carniola).
This form is confined to the countries north of the Mediterranean Sea. Some
specimens from West Algeria and Morocco approach this almost indistinguishably,
but alongside of them occur the strange medley of colour varieties treated under
the next subspecies.]
294. Erastria trabealis deleta (Stand.).
Agrophila deleta Staudinger, Stetl. Entom. Zeit. vol. xxxviii. p. 190 (1877) (Algeria).
Agrophila flavonitens Austaut, Le Xat. vol. ii. pt. xbc. p. 156 (1880) (Sebdou).
Emmelia sulphuralis var. algira Oberthiir. EUid. Entom. livr. vi. p. 90. pi. 2. f. 2 (1881) (Bone).
I have given the full synonymy of the Mauretanian race of trabealis because
there has been considerable confusion as to the status of the forms to which
the three names apply. Mr. Oberthur's algira is the aberration with the black
markings reduced ; deleta is the form where the black is reduced to one mark only ;
and flavonitens is the aberration with no black on the forewings. The specimens
from Morocco and West Algeria in which the black markings are practically the
same as in Europe I propose to call ab. parallela ab. nov. and the aberration with
all the black markings replaced by stramineous olive I call ab. olivina ab. nov.
At Tring we have 170 Mauretanian specimens, of which 12 are ab. parallela
and 4 halfway between that and algira, and 18 are algira ; the remaining 136 are
mixed flavonitens, deleta, and olivina. The 160 are from Mazagan, Morocco, April —
June 1902 (W. Riggenbach) ; Biskra, April 1908 (W. R. and E. H.) ; Sidi-bel-
Abbes, May— August 1916-1917 (M. Rotrou) ; Masser Mines, June 1914 (V.
Faroult) ; Sebdou, Foret de Tenira, July 1918 (P. Rotrou) ; Rabat, May 1913 (A.
Thery).
The British Museum has 1 $ Biskra, March 1897, A. E. Eaton.
295. Tarache lucida (Hufn.).
Noctua lucida Hufnagel, Bert. Mag. vol. iii. p. 302 (1766) (Berlin).
This is a very variable species, occuring almost black = ab. lugens Alph. and
almost white = ab. insolatrix Hiibn. ; in between are the aberrations albicollis
Fabr. and Solaris Oberth., but much whiter specimens exist than ab. insolatrix,
and I propose the name ab. extremaab. nov. for the specimens with only a dark
border and a few black dots in the white disc.
We have at Tring 427 Mauretanian examples from Mazagan and Cape Blanco
May— October 1902, Imitanut May 1904, Truchan May 1904, Rohama April-
May 1903, Seksawa April 1905, Morocco (W. Riggenbach) ; Oum-re-Biah, Morocco,
Novitates Zoolooicae XXVTI. 1920. 75
April 1901 (Hartert): Biskra, March— April 1908-1914 (W. R. and E. H.); El
Kantara February — May 1909, Hammam Meskoutine May 1909 (W. R. and
E. H.) ; Environs d' Alger (Dr. Nissen) ; Casba, Alger (Captain Holl) ; Khenchela
May 1912, Hammam Meskoutine May 1914, Souk Ahras April 1914 (W. R. and
K. J.) ; Environs de Batna, 1913-1914 (A. Nelva) ; El Kantara March— August
1911-1917, Masser Mines May 1914, Ain Draham July 1911, Perregaux October
1915, Hammam R'hira April — June 1916-1917, Berrouaghia April 1914, Bou
Saada and Djebel Kerdada May 1912, El Hamel May 1912, El Mesrane June
1913, Oued Hamidou June 1912, Terres Blanches May 1913, Guelt-es-Stel April-
September 1912-1913, La Macta, Perregaux September 1915, Lalla Marnia and
Moroccan Frontier May 1914, Puits Baba May 1913, Laghouat March 1912,
Mecheria May 1918, Nedroma May 1914, Msila May 1915 (V. Faroult) ; Sidi-bel-
Abbes July — September 1916 (M. Rotrou) ; Belvedere, Tunis, August — September
1915 (E. Blanc) ; Sebdou, August 1918 (P. Rotrou) ; Oued Nca, April 1914
(Hartert and Hilgert) ; Environs d'Alger, May 1911 (W. R. and E. H.) ; Oran,
April 1913 (W. R. and E. H.) ; Les Pins, September, 1918 (M. Rotrou) ; Grottes de
Tafna, Ain-El-Berd July— September 1918 (P. Rotrou) ; Rabat, Morocco, June
1913 (A. Thery).
The British Museum has 1 (J, 1 $ Algeria, Mrs. Nicholl ; 1 $ Philippeville
1 ? Hammam-es-Salahin March— May 1904, Lord Walsingham ; 1 $ Tangier, 1 <j|
1 $ Mogodon, Leech ; 1 Biskra, April 1903, A. E. Eaton.
296. Tarache biskrensis (Oberth.).
Aconlia biskrensis Oberthiir, Bull. Soc. Entom. France, 1887. p. 58 (Biskra).
We found this species far from common.
The series at Tring numbers 63 from Colomb Bechar March — April 1912,
Bou Saada May 1912, Djebel Kerdada May 1912, El Outaya August 1910, El
Hamel May 1912, Ain Draham September 1911 (V. Faroult) ; Ghardaia, April
1911 (W. R, and E. H.) ; Oued Nca April 1914, Sidi Hassi Mahmud April 1914,
Oued Abiod May 1912, El Alia May 1914, north of El Golea, halfway between
Ouargla and El Golea, Hassi el Hadjar, South Oued Mya March— May 1912
(Hartert and Hilgert).
This species is apparently as variable as lucida.
297. Acontia luctuosa (Schiff. and Den).
Phalaena luctuosa Schiffermiiller and Denia, Ank. Syst. Werk. Schmett. Wienergcg. p. 90 (1775) (Vienna).
Of this species we have at Tring 259 Mauretanian specimens from Mazagan,
Morocco June— August 1900-1903 (W. Riggenbach) ; Environs d'Alger, May
1908-1912 (W. R., E. H., and K. J., and Dr. Nissen) ; Sidi Ferruch, August 1911
(A. Thery) ; Batna (A. Nelva) ; Hammam Meskoutine, May 1914 (W. R. and
K. J.) ; Sidi-bel-Abbes, July— August 1916-1917 (M. Rotrou) ; Hammam R'hira,
May— June 1911-1917 (W. R. and E. H., and Faroult) ; Perregaux September
1915, Zoudj el Beghal July 1914, Masser Mines May 1914, Environs de Setif 1911,
Tizi Ouzou July 1914, Debrousseville September 1914, north side of Djebel Zaccar
August 1916, Ain Draham September 1911 (V. Faroult) ; Rabat, Morocco, June
1913 (A. Thery).
76 Novitates Zoolooicae XXVII. 1920.
298. Lipatephia eremophila (Rebel).
Armada eremophila Rebel, Verh. Zool.-Bot. Gesell. Wien, vol. xlv. p. 350. No. 10 (1895) (Ouargla-
Ghardaia).
Armada lacroixi D. Lucas, Bull. Soc. Enlom. France, p. 312 (1914) (Tunis).
This pretty species has been entirely misunderstood. Mr. William Warren
in Seitz figures and describes a totally different insect, entirely ignoring Rebel's
statement that the forevving of his eremophila had a general resemblance in colour
and pattern to Aedia funesta (Esp.). Dr. Rebel's name has priority over Monsieur
Daniel Lucas's by twenty years, but Mr. Oberthiir and his friends will not agree
as Dr. Rebel gives no figure.
We have at Tring 15 specimens from Ghardai'a, April 1911 (W. R. and E. H.) ;
Ain Sefra March 1915, Colomb Bechar March— April 1912 (V. Faroult).
There is 1 specimen of ours from Ghardaia in the British Museum.
299. Nereisana oranaria (Luc).
Chesias oranaria Lucas, Explor. Scient. d'Algerie, vol. iii. p. 392. No. 132. pi. 4. f. 4 (1848) (Oran).
This insect was considered by its author to be a Geometer, and Mr. Oberthiir
and others have followed him, but it is really a Noctuid and belongs to the
Erastriinae.
I have a single pair of this rare species.
1 ? Souk Akras, April 1914 (W. R. and K. J.) ; 1 $ Environs d'Alger, Feb-
ruary 1908 (W. R. and E. H.).
The British Museum has 2 ?$ Algeria, Mrs. Nicholl ; 4 £<$ Hammam Mes-
koutine, March 1911, Meade- Waldo.
300. Hadjina viscosa (Frr.).
Mythimna viscosa Freyer, Neu. Beitr. vol. i. p. 39. pi. 21. f. 3 (1831) (Sicily).
Victor Faroult caught two specimens of this species during his unfortunate
trip to Perregaux, whence he had to flee for his life.
1 {J, 1 $ Perregaux, September 1915 (V. Faroult).
301. Iambiodes incerta (Rothsch.). (PI. XVI. f. 1.)
Bryophila incerta Rothschild, Novil. Zool. vol. xx. p. 125. No. 51 (1913) (Oued Nca).
This is almost certainly the insect Mr. Oberthiir enumerates under the
name of Erastria juscula gueneei Fall.
If this is so, it has been wrongly identified by Mr. Oberthiir, for the insect
here enumerated is certainly not Lithacodia fasciana gueneei (Fall.).
There are 7 specimens of this rare species at Tring from Oued Nca, April — June
1912-1914 (Hartert and Hilgert).
302. Eublemma scitula (Ramb.). (PI. XVI. ff. 21, 22.)
Erastria scitula Rambur, Ann. Soc. Entom. France, 1833. p. 26. pi. ii. f. 16 (Corsica).
Mr. Oberthiir remarks that he has no personal knowledge of this species
having occurred in Algeria, but he was convinced it had been taken, and therefore
included it.
Novttates Zoolooicae XXVII. 1920. 77
1 have received 35 specimens of it from Monsieur Maxime Rotrou and
others. It is very strange that I never received it either from Tlemcen or Sebdou,
seeing that these places produce great numbers of olive trees. The strange
habits of the larva in being carnivorous and living on the Coccid (Lecanium oleae)
are not unique, many of the tropical species of Eublemma feeding on Coccidae.
21 Sidi-bel-Abbes, August— September 1915-1918 (M. Rotrou) ; 1 Ras
Chergui, Ain Sefra July 1915 (V. Faroult) ; 9 Foret de Tenira, September 1918
(P. Rotrou) ; 2 Messer, September 1917 (M. Rotrou) ; Sidi Ferruch, July 1911
(A. Thery).
303. Catablemma geyri (Rothsch.). (PI. XVI. 1 23.)
Eublemma geyri Rothschild, Ann. Mag. Nat. Hist. (8). xvi. p. 252. No. 28 (1915) (Tahihout).
Of this species I only have 4 specimens.
3 $$ Tahihout, April 1914 (Geyr von Schweppenburg) ; 1 $ Ain Sefra, July
1915 (V. Faroult).
304. Eulocastra diaphora (Stdgr.).
Brastria diaphora Staudinger, Hor. Entom. Soc. Ross. vol. xiv. p. 415 (1878) (Kerasdere, Asia Minor),
Of this I have received 7 specimens.
2 South Oued Mya, May 1912 (Hartert and Hilgert) ; 1 Colomb-Bechar,
March 1912 (V. Faroult) ; 4 Oued-Gif-Aman, Oued Tamoudat, Oued Ahmra,
Ti-n-Tabarik March — April 1914 (Geyr von Schweppenburg).
The British Museum has 1 <J, 3 ?? Hammam-es-Salahin, April — May 1903-
1904, Lord Walsingham.
[Phyllophila numerica (Boisd.).
Agrophila numerica Boisduva!, Gen. et Ind. Meth. edit. ii. p. 175. No. 1403 (1840) (Corsica).
There have been 3 subspecies described : disjecta Warr. from Spain, not
Sardinia as Mr. Oberthur states ; ornatula Christ, from Turkestan ; and deserti
Oberth. from El Outaya, Algeria. Both Mr. Warren and Sir George Hampson
make ornatula occur in Algeria, while Mr. Oberthur denies it, while erroneously
applying disjecta Warr. to the large strongly marked Sardinian form. In addition
to my 12 Algerian examples there are at Tring 9 European specimens, 7 from
Sardinia and 2 without locality. The two latter appear to be typical numerica.
As Mr. Oberthiir has erroneously applied Mr. Warren's name disjecta to the
Sardinian form, in spite of the fact that in Seitz Mr. Warren expressly states
that his name disjecta was given to the Ab. 1 of Hampson and its habitat was
Spain, in order to prevent the perpetuation of the error I propose the name
numerica sardoa subsp. nov. for the Sardinian form, which differs from n. numerica
in its larger size and more conspicuous pattern.
The 11 Algerian specimens consist of 1 from Sebdou, 2 from Guelt-es-Stel,
2 from Bou Saada, and 7 from Ain Sefra. The 1 from Sebdou, 1 from Guelt-es-
Stel, and 4 from Ain Sefra agree well with Guenee's figure of the Andalusian $,
while the 6 others agree with " var. deserti Oberth." This proves deserti not to be
a local race, but simply an aberration, and that the Algerian form is disjecta Warr.]
78 NOVITATES ZOOLOGICAE XXVII. 1920.
305. Phyllophila numerica disjecta Warr.
Phyllophila numerica ab. disjecta Warren in Seitz, Grossschmett. Erde, vol. iii. p. 274 (Spain).
3 ?$ Sebdou, June 1918 (P. Rotrou) ; 1 (J, 1 $ Guelt-es-Stel, May— Septem-
ber 1913 (V. Faroult) ; 2 J^J, 1 $ Bou Saada, May 1911 (V. Faroult) ; 3 <£<£, 4 ?$
Aln Sefra, May^July 1913-1915 (W. R. and K. J., and Faroult).
Of these the <$ from Guelt-es-Stel, the 2 <$<$, 1 ? from Bou Saada, 1 $ from
Sebdou, and 1 $, 2 $$ from Aln Sefra, are ab. deserti Oberth.
[Eublemma velox (Hiibn.).
Noetaa velox Hiibner, Samml. Eur. Schmett. Noct. B. 507, 515 (1818).
Mr. Oberthur does not mention this form, only velox velocior Stdgr.
Mr. Warren has described a $ from Algeria ! as griseimargo which differs in
being larger and more suffused with red ; I have a second still larger specimen
of this form from Bou Saada. Although Mr. Warren's name was given to an
aberration it will have to stand for the Algerian subspecies which differs from the
type in being larger and less grey. The form velocior Stdgr. from Sicily is very
distinct.]
306. Eublemma velox griseimargo (Warr.).
Leptosia griseimargo Warren, Novil. Zool. vol. six. p. 36. No. 79 (1912) (Algeria).
My series consists of 31 specimens from Algeria : Bou Saada April — May
1911, Lalla Marnia May 1914, Perregaux September 1915 (V. Faroult) ; Hammam
Meskoutine, May 1914 (W. R. and K. J.); Ain Draham, September 1911 (V.
Faroult) ; Guelt-es-Stel, October 1913 (V. Faroult) ; Foret de Tenira, Sebdou
June — September 1918 (P. Rotrou) ; Les Pins August, Environs de Taourirt
July 1918 (M. Rotrou) ; Rabat (A. Thery) ; Mazagan, September 1903 (W.
Riggenbach).
[Eublemma polygramma (Dup.).
Anthophila polygramma Duponehel, Lipid. France, Suppl. III. p. 519. pi. 44. f. 3 (1836) (Digne).
I have never received this species.]
307. Eublemma permixta (Stdgr.) (PI. XVI. ff. 1-5.)
Thalpochares permixta Staudinger, Iris, vol. x. p. 266. pi. 4. f. 7 (1897) (Chellala).
Eublemma mozabitica Rothschild, Novit. Zool. vol xix. p. 126. No. 5 (1912) (Ghardaia).
I am confident that my fellow- lepidopterists will not blame me very much
for having redescribed permixta Stdgr. ; for I believe nine out of ten would have
done so, if they had compared my type with the sandy yellow specimens of this
variable insect in the British Museum or with Staudinger's original description,
where the ground-colour is given as grey- green marked with brown.
As it turns out on examination of more specimens, there are intermediate
specimens between my mozabitica and the extreme sandy yellow form, but so far
we have no example at Tring agreeing with Staudinger's original description.
I propose to call the sandy yellow form ab. arenosa ab. nov. and the inter-
mediate form ab. intermedia ab. nov., while the specimens with violet-mauve
ground-colour will stand as ab. mozabitica Rothsch.
Novitates Zoolooicae XXVII. 1920. 79
We have at Tring 23 specimens from Ghardaia April 1911, Ain Sefra May 1913
(W. R. and E. H.) ; halfway between Ouargla and El Golea March 1912, South
Oued Mya April 1912, Oued Nca April 1914 (Hartert and Hilgert) ; BouSaada,
March— May 1911-1912 (V. Faroult).
Of these 23 examples, 10 are ab. mozabitica, 5 ab. arenosa, 7 ab. inter-
media., and 1 ab. nivescens.
The extreme white form is ab. nivescens ab. nov.
The British Museum has 1 $ Hammam-es-Salahin, May 1906, Lord Walsing-
ham (type of ab. nivescens).
308. Eublemma parva (Hiibn.).
Noctua parva Hiibner, Samml. Eur. Schmett. Noct. f. 356 (1808).
This species is almost as variable as ostrina, going from cream- colour without
markings to specimens with basal half of forewing chestnut- brown and outer half
almost black.
The series of Mauretanian examples at Tring comprises 177 from Mazagan,
July 1900 (W. Riggenbach) ; Hammam R'hira, May— June 1913-1916 (W. R.
and E. H., and Faroult) ; Sidi Ferruch, July 1911 (A. Thery) ; GuehVes-Stel
November 1913, Perregaux September 1915, Lalla Marnia May 1914 (V. Faroult) ;
Ain Sefra, May— June 1913-1915 (W. R. and E. H., and Faroult) ; Sebdou, June
— September 1918 (P. Rotrou) ; Sidi-bel-Abbes, June — October 1916-1918 (M.
Rotrou) ; Sebdou, El Misale, June — September 1918 (P. Rotrou) ; A'inDouz, Les
Pins, Environs de Taourirt, July — August 1917-1918 (M. Rotrou) ; La Mocta,
September 1915 (V. Faroult).
Of the 177 specimens 74 are from Sidi-bel-Abbes and 51 from Sebdou.
In the British Museum are 1 $ Hammam-es-Salahin, April 1904, Lord
Walsingham ; 1 <j> Batna, August 1910, E. A. Eaton ; 1 Tozeur, Tunisia, 1913,
G. C. Champion ; 1 $ Tangier, Leech coll.
309. Eublemma deserti (Rothsch.). (PI. XVI. f. 26.)
Thalpocluires deserti Rothschild, Entom. Zeit. Stuttgart, vol. xxiii. p. 142 (1909) (Mraier).
This very rare species at first sight looks like a minute washed-out parva,
but in reality it belongs to a different section of the genus.
2 <J<J Mraier, April 1909 (W. R. and E. H.) ; 1 $ Ain Taiba, May 1914 (Geyr
von Schweppenburg).
310. Eublemma cochylioides (Guen.).
Micra cochylioides Guenee, Hist. Nat. Ins. Spec. Gen. Lipid, vol. vi. Noct. vol. ii. p. 245 (1852) (Island
of Bourbon).
This beautiful little species has a very wide distribution, ranging from the
Canary Islands to Australia and the Fiji Islands.
1 cj Sidi-bel-Abbes, July 1916 (M. Rotrou).
This specimen is very bright, especially the yellow of the thorax and basal
one-third of forewings.
80 Novitates Zoologicae XXVII. 1920.
311. Eublemma ostrina (Hiibn.).
Noctua ostrina Hiibner, Samml. Eur. Schmett. Noel. ff. 399, 648 (1808).
We find in Algeria all the forms of this extremely protean species from ab.
cartliami H.-S. uniform yellowish to the darkest ab. porphyrina Frr., with abs.
numida Lucas, purpurata Led., aestivalis Guen., and a host of others more or less
intermediate.
We have at Tring a Mauretanian series of 287 examples from Guelt-es-Stel
March— May 1912-1913, Hammam R'hira May 1913-1916 (W. R., E. H., and
K. J., and Faroult) ; north side of Djebel Zaccar August 1916, Tilghemt April
1912, Masser Mines June, Lalla Marnia May 1914, Ain Draham May 1911, El
Kantara August 1917, Mecheria and Djebel Antar May 1918, Ain Sefra June
1915, Bou Cedraia May 1913, Bordj-ben-Aneridj November 1911, Oued Hamidou
June 1912, Bou Saada March 1912 (V. Faroult) ; Environs de Batna, 1913-1914
(A. Nelva); Sidi Ferruch, July 1911 (A. Thery) ; Sidi-bel-Abbes, Ain Dour,
June — August 1916-1917 (M. Rotrou) ; Sebdou, Foret de Tenira, August 1918
(P. Rotrou) ; Environs d'Alger May 1912, Khenchela May 1912, Hammam Mes-
koutine April— May 1914, Souk Ahras April 1914 (W. R. and K. J.) ; Ghardaia
April 1911, Biskra 1911, Oran April 1913, Tlemcen April 1913 (W. R. and E. H.) ;
Rabat, July 1913 (A. Thery); Environs de Taourirt, July 1918 (M. Rotrou);
El Mahouna, July 1919 (V. Faroult).
The British Museum has 3 9$ Algeria, Mrs. Nicholl ; 1 $ Philippeville, 2 <$$,
4 $?, 1 larva, Hammam-es-Salahin, April — May 1904, Lord Walsingham ; 1 <$ El
Kantara, April 1913, P. A. Buxton ; 1 <J Morocco, Stainton coll. ; 6 <$$ Tangier,
Leech coll.
312. Eublemma pseudostrina Rothsch. (PI. XVI. f. 25.)
Eublemma pseudoslrina Rothschild, Novit. Zool. vol. xxi. p. 339. No. 210 (1914) (Guelt-es-Stel).
At first sight this might be mistaken for one of the innumerable varieties of
ostrina, but the sooty-grey fringe and apex at once distinguish it.
1 $ Guelt-es-Stel, August 1913 (V. Faroult).
313. Eublemma subvenata (Stdgr.).
Thalpochares subvenata Staudinger, Iris, vol. v. p. 288. No. 64. pi. iii. f. 13 (1892) (Tunis).
4 Ain Sefra, July 1915 (V. Faroult).
In the British Museum is 1 $ El Kantara, May 1903, Lord Walsingham.
[Eumegethes tenuis (Stdgr.).
Thalpochares (Eumegethes) tennis Staudinger, Iris, vol. x. p. 268. pi. iv. f. 6 (1S97) (Sfax).
Mr. Oberthiir states that he is doubtful what family this belongs to ; this
shows that because he will not acknowledge unfigured species, he also ignores
all the rest of articles in which such unfigured species may be described.
In my article on the " Lepidopterous Fauna of Guelt-es-Stel " in vol. xxi.
Novit. Zool. p. 341, No. 228, I expressly point out that both Mr. Prout and Mr.
William Warren had examined the insect and found it to be a Geometer and not
a Noctuid.
NOVITATES ZOOLOGICAE XXVII. 1920. 81
Its right position is in the subfamily Oenochrominae, and Mr. Prout places it
immediately after Myinodes inter punctaria Herr.-Sch. and in front of Theozena
tenuis Meyr.
The series at Tring consists of 45 examples from Guelt-es-Stel, November
1913 (V. Faroult).]
314. Eublemma albida (Dup.).
Anthophila albida Duponchel, Lipid. France, Suppl. iv. p. 382. pi. 81. f. 1 (1842) (Marseilles).
Mr. Oberthiir figures specimens of ab. gratissima Stdgr. from the Djebel
Aures, and the ab. brunnescens Culot is from Lambessa.
Among the 65 examples at Tring only typical albida and ab. albidior Culot
are represented from Algeria and gratissima from Tunis.
46 Environs de Batna, June 1900-1914 (Dr. A. Seitz and A. Nelva) ; 6 Tunis
Dannehl, 10 Sebdou El Misab, June — July 1918 (P. Rotrou) ; 1 Hammam R'hira,
June 1916 (V. Faroult)'; 1 Ain Fezza, June 1917 (M. Rotrou); El Mahouna, July
1919 (V. Faroult).
315. Eublemma grata (Guen.).
Anthophila grata Guenee, Hist. Nat. Ins. Spec. Gen. Lipid, vol. vi. Noct. ii. p. 251. No. 1048 (1852)
(South Spain).
Of this species a number of forms have received names, viz. albicans Ramb. ;
candicans Ramb. ; extranea Ramb. ; extraria Ramb. ; faroulti Rothsch. ; and
ramburi Culot. Of these all but faroulti Rothsch. = ramburi Culot are un-
doubtedly only aberrations. The status of faroulti is rather more complex ; while
it undoubted^ occurs as an aberration among the other forms of grata, the fact
remains that in the Guelt-es-Stel region it forms the bulk of the specimens, but I
fear this is not sufficient to give it the rank of subspecies. Therefore the aberra-
tions are as follows :
ab. albicans Ramb., white, pattern obsolete.
ab. candicans Ramb., white, pattern distinct, lines narrow.
ab. faroulti Rothsch., white, pattern heavy, lines very broad.
ab. extranea Ramb., greyish white, pattern medium.
ab. grata Boisd., greyer, pattern feeble.
ab. extraria Ramb., grey-brown, pattern strong.
In the British Museum Catalogue Sir George Hampson has grata and candi-
cans as two species, but this is natural in view of the very few specimens he
had for comparison.
The series at Tring consists of 173 examples from Guelt-es-Stel May — June
1913, Bou Saada May 1911-1912, El Hamel May 1912, Zmila nr. Oran June
1913, Terres Blanches and Puits Baba May 1913 (V. Faroult) ; Batna, July 1910
(Dr. A. Seitz and A. Nelva) ; Sebdou, June 1918 (P. Rotrou) ; Les Pins, July
1917 (M. Rotrou).
In the British Museum are 1 <$ Bou Saada ; 2 <JJ Guelt-es-Stel ex Tring
Museum.
[Eublemma albicans (Guen.).
Anthophila albicans Guenee, Hist. Nat. Ins. Spec. Gen. Lipid, vol. vi. Noct. ii. p. 251 (1852)
(Andalusia).
The confusion surrounding this species is astounding, and the examination
of the Uterature has been worse than perfunctory. We have to thank Messrs.
6
82 Novitates Zoolooicae XXVII. 1920.
Oberthiir and Culot for the final solution ; though even Mr. Oberthiir has not
got it quite right. The error arose in the first place by Boisduval, in his Genera
and Index Melhodicus, edit. ii. 1840, p. 104, No. 1314, giving "Albicans Ramb.
Faun. Andal." Now Rambur's Faune de I'Andaloitsie, although evidently more
complete in manuscript, was never fully published. Of the Lepidoptera, pages
213-330 of text and pi. 8-18 of figures are all that has appeared, the text running
from Papilio podalirius to Sesia rltingiaejormis and the plates from Zegris to the
Hesperidae among the Diurni and from Zygaena to Caradrina among the Nocturni.
Thus Boisduval's Haemerosia, including albicans, was never published in that
work. In 1858-1800 Rambur, however, published his Catalogue Systematique
des Lepidopteres de V Andalousie, pp. 1-412 and Plates 1-22 ; the text, however,
was never completed and probably some plates also are wanting, as livraison iii.,
which was to complete the work, was never published. Page 412 ends up with
Pterostoma palpina unfinished, so that there is no text to the plates- 0-22, but
as the figures are named, the new species stand good.
On plates 10. ff. 4, 5 ; 13 f. 2 and 15 f. 1 Rambur figures four aberrations, to
one of which he gave the name albicans, of a very different Eublemma to the one
he proposed to call albicans in that part of the Faune never published.
Meanwhile, however, Guenee in 1852 described as albicans (see above) the
specimen in Boisduval's collection which was to have been published by Rambur
as albicans in the Faune ; and as he gives a very good description and his type
exists (see Culot, Noct. et Geom. d'Eur. pt. i. vol. ii. pi. 00, f. 15), albicans must
stand for that species.
Sir George Hampson in the Catalogue has divided albicans Ramb. (nee
Guen.) = grata Guen. into two species, candicans Ramb. and grata Boisd. (see
vol. x. pp. 125 and 155), and placed both albicans Guen. and albicans Ramb. under
grata, quite failing to grasp the truth owing to the great confusion due to the non-
publication of the part of Rambur's Fcmne containing the original figure and
description of Boisduval's albicans. The correct solution of this complicated
question is that there are two species grata Guen. and albicans Guen. But albicans
Ramb., candicans Ramb., extranea Ramb., and extraria Ramb. are all colour
variations of grata Guen. (see antea sub. No. 314), while albicans Guen. is a distinct
species.
.Mr. Oberthiir records 2 specimens of this species from El Outaya, but I have
never received it.]
310. Eublemma virginalis (Oberth.).
Anthophila virginalis Oberthiir, Etud. Entom. livr. vi. p. 90. pi. xi. f. 1 (18S1) (Sebdou).
Anlliophila caid Oberthiir ( = ab. caid), Etud. Entom. livr. vi. p. 91. pi. xi. f. 2 (1881) (Sebdou).
Eublemma subterminalis Rothschild, Novit. Znol. vol. xxi. p. 338. No. 209 (1914) (Guelt-es-Stel).
I have 82 examples, other than from Guelt-es-Stel, of this species, and that
I consider too few to say anything about it, beyond that I agree with Mr. Oberthiir
in his recent conclusion that his caid is only an aberration of virginalis. My
subterminalis is a pure synonym of virginalis, and due to carelessness on my part.
Of ab. caid there are 54 specimens and 28 virginalis among the 82 not from
Guelt-es-Stel. All the 112 from Guelt-es-Stel are virginalis.
The Tring series totals 194: 112 Guelt-es-Stel, June— July 1913, 1
Djelfa June 1913 (V. Faroult) ; 5 Am Sefra June— July 1915, 1 Bou Saada
N'OVITATES ZOOLOOICAE XXVII. 1920. 83
May 1911 (V. Faroult) ; 15 Sebdou July— August 1918, 2 El Mizab, Foret de
Tenira (P. Rotrou) ; 1 Sidi-bel-Abbes July 1917 (M. Rotrou) ; 49 Les Pins,
August 1918 (M. Rotrou) ; 8 Environs de Taourirt July 1918 (M. Rotrou).
317. Eublemma emir (Culot).
Thalpochzres emir Culot, Noel, et Giom. d'Eur. pt. i. vol. ii. p. 153. pi. 68. f. 4 (1916) (Geryville).
Of this insect I have a very poor series, 9 Guelt-es-Stel June — July 1913 (V.
Faroult).
318. Eublemma deserta (Stdgr.).
Thalpochares deserta Staudinger, Iris, vol. xii. p. 383 (1899) (Biskra).
Of this purely desert species we have at Tring 47 specimens, 2 from north of
and 45 from south of In Salah.
1 $ north of Ai'nGuettera, 1 $ S. Oued Mya, April 1912 (Hartert and Hilgert) ;
45 Timassinin, Oued Ag'elil, Oued Dehin, Ideles, 20 kil. N. of Ideles, Oued
Tamoudat, Oued Ahmra, Aceksem, Ti-n-Tabarik, Ai'n Tahart, Amgid, and
Tahihout, Hoggar Mts. and Desert N. of Hoggar Mts. January — April 1914 (Geyr
von Schweppenburg).
In the British Museum are 1 ^ Biskra, Staudinger and Bang-Haas ; 1 $
Hammam-es-Salahin, May 1903, Lord Walsingham.
319. Eublemma arida Rothsch. (PI. XVI. f. IS.)
Eublemma arida Rothschild. Novit. Zool. vol. xx. p. 127. No. 65 (1913) (S. of El Golea).
1 (J, 1 $ S. of El Golea, May 1912 (Hartert and Hilgert).
320. Catablemma cremorna Hmpson. nom. nov.
Catahlemma conistrota Hampson, part., Cat. Lepid. Phal. Brit. Mies. vol. x. p. 192. No. 5296. pi. cliv.
i. 29 (1910) (Beloochistan).
cj$. Head and thorax white ; abdomen cream colour, washed with pale
yellowish grey.
Forewings costal area white, rest of wings and fringe yellow-grey powdered
with black scales, more densely between the nervures. Hindwings yellowish grey.
Length of forewing : largest 12 mm., smallest 9 mm.
Expanse: largest 27 mm., smallest 20 mm.
In British Museum 1 $ Tozeur, South Tunisia, 1913 (G C. Champion) (type).
The series at Tring numbers 61 from Ain Sefra, May 1913-1915 (W. R. and
E. H., and Faroult) ; Hassi Sidi Mahmoud, Hassi Dinar, El Alia, E. of Guerrara
Oued Nca April 1914, El Meksa April, S. of El Golea, South Oued Mya May 1912
(Hartert and Hilgert) ; Oued Abiod, April 1912 (Hartert and Hilgert) ; Fontaine
Chaude, April 1909 (W. R. and E. H.) ; Colomb-Bechar, March— April 1912
(V. Faroult).
321. Eublemma ernesti Rothsch.
Eublemma ernesti Rothschild, Novit. Zool. vol. xxii. p. 232. No. 38 (1915) (Oued Nca).
The 5$ and the 1^1 placed with this species, on closer examination prove
not to belong here.
1 <5 (type) Oued Nca, April 1914 (Hartert and Hilgert) ; 1 <$ Ain Sefra, May
1913 (W. R, and E. H.).
84 Novitates Zoolooicae XXVII. 1920.
322. Eublemma albivestalis Hmpsn.
Eublemma albivestalis Hanipson, Cat. Lepid. Phal. Brit. Mus. vol. x. p. 191. No. 5292. pi. oliv.
f. 25 (1910) (Dead Sea).
3 $$ Oued N9a, April 1914 (Hartert and Hilgert) ; 2 <J<J, 7 $$ Les Pins, May
—August 1918 (M. Rotrou) ; 1 <J Sebdou, September 1918 (P. Rotrou).
323. Eublemma wollastoni N. C. Rothsch.
Eublemma wollastoni N. C. Rothschild, Novit. Zool. vol. viii. p. 430. No. 27 (1901) (Sheiuji).
3 $$ Oued Nca, April 1914 (Hartert and Hilgert).
324. Eublemma lacteola Rothsch.
EubUmma lacteola Rothschild, Novit. Zool. vol. xxi. p. 339. No. 210 (1914) (Guelt-es-Stel).
15 from Guelt-es-Stel, May 1913 (V. Faroult) ; Am Sefra, May — July 1913-
1915 (W. R. and E. H., and Faroult) ; South Oued Mya May 1912, Oued Nca
April 1914 (Hartert and Hilgert) ; Ras Chergui, July 1915 (V. Faroult).
325. Eublemma albidior Rothsch.
Eublemma albidior Rothschild, Ann. Mag. Xat. Hist. (8) xvi. p. 253. No. 30 (1915) (Oued Ahmra).
4 I deles, Oued Ahmra, Amgid, north of and in Hoggar Mts., March — April
1914 (Geyr von Schweppenburg) ; 2 Ai'n Guettera May 1912, Oued Nca April
1914 (Hartert and Hilgert).
326. Eublemma pernivea sp. nov. (PI. XVI. f. 20.)
cJ $. Dazzling snow-white all over.
Length of forewing, 10 mm. ; expanse, 22 mm.
4 (JcJ, 1 ? Am Sefra, May— August 1913-1915 (W. R. and E. H., and V.
Faroult) ; 1 $ Sebdou, August 1918 (P. Rotrou) ; 1 $ Les Pins, September 191S
(M. Rotrou). (? Ain Sefra, type.)
327. Eublemma crocea sp. nov. (PI. XVI. f. 19.)
$. Head dark yellow ; thorax and abdomen yellow-buff. Forewings saffron-
yellow ; hindwings cream-colour.
Length of forewing, 9 mm. ; expanse, 20 mm.
1 $ A'in Tahart, north of Hoggar Mts., April 1914 (Geyr von Schweppenburg).
I had thought this was a very bright aberration of deserta Stdgr.
328. Eublemma confusa sp. nov.
<J $. These 1 7 specimens had been mixed up with and mistaken for cremarna.
They can at once be distinguished by the strongly produced acutely pointed apex
of the forewing and the dark line running in from apex. Also by the strange
accentuation of the median fold.
cJ$. Head white, rest of insect whitish grey. Forewings irregularly dusted
with black scales, subapical area washed broadly with rusty yellow, a dark line
running in obliquely from apex ; central fold very deep and abnormally developed,
Novitates Zoolooicae XXVII. 1920. 85
as is a shorter fold below, both strongly powdered with black scales. Hindwings
darker grey, with pale fringe.
Length of forewing : <J 8 mm., $ 11 mm. ; expanse, $ 18 mm., $ 24 mm.
4 <$<$, ! ? Oued Nca, April 1914 (Hartert and Hilgert) ; 1 $ Ain Sefra, June
1915 (V. Faroult) ; 1 $ Gharda'ia, April 1911 (W. R. and E. H.).
[Eublemma lacemaria (Hiibn.).
Geomctra lac.ernaria Hiibner, Samml. Eur. Schmett. Geom. f. 422 (1818).
Antkophila glarea Treitschke, Eur. Schmett. vol. v. pt. 3. p. 282. No. 6 (1826) (Dalmatia).
I have never received this species.]
[Eublemma suava (Hiibn.).
Noctua suava Hiibner, Samml. Eur. Schmett. Noct. f. 578 (1818).
Mr. Oberthiir places Rambur's blandula ^ pergrata $ as a form of suava, and
says this is the Algerian race. Mr. Culot places Rambur's insect as a race of
arcuina, although acknowledging it to be nearer suava.
I have 1 $ from Sidi Ferruch which is red like the <J<J, but my other 6 $$ are
all sooty slate-grey. There is, however, an apparently constant difference from
European suava in that the black basal portion of the postmedian band is much
broader, therefore I shall place the Algerian race for the present under Rambur's
name, until it is possible to compare a good series from Spain with Algerian
material.]
329. Eublemma suava blandula (Ramb.).
Noctua blandula Rambur, Cat. Syst. Lipid, de V And. pi. x. f. 2 (1858) (Andalusia).
Sir George Hampson has put blandula as a synonym of arcuina ; this is at
once disproved by the non angulate postmedian band.
We have 9 £<$, 1 1 ?? from Mauretania : Mazagan, Morocco, September
1902 (W. Riggenbach) ; Sidi Ferruch, July 1911, Rabat (A. Thery) ; Masser
Mines June 1914, Ain Draham July 1911, Perregaux September 1915, Blida
November 1915 (V. Faroult) ; Hammam Meskoutine, May 1914 (W. R. and E. H.) ;
Sebdou, Foret de Tenira, June — September 1918 (P. Rotrou) ; El Mahouna,
September 1919 (V. Faroult).
330. Eublemma syrtensis Hmpsn.
Eublemma syrtensis Hampson, Cat. Lepid. Phal. Brit. Mus. vol. x. p. 112. No. 5137. pi. cli. f. 28
(1910) (Hamniam-es-Salahin).
The type in the British Museum has hitherto been unique ; 1 $ Hammam-
es-Salahin (Lord Walsingham).
The small series at Tring shows no 'variation. 7 <J^ Environs de Batna,
1913-1914 (A. Nelva).
331. Eublemma jucunda (Hiibn).
Noctua jucunda Hiibner, Samml. Eur. Schmett. Noct. ft". 486, 492 (1S18).
Our series from Mauretania of this contains 43 specimens from Sidi-bel-
Abbes, July — October 1916-1917 (M. Rotrou) ; Masser Mines June 1914, Ain
Sefra June 1915, Guelt-es-Stel August 1913 (V. Faroult) ; Sebdou, Foret de
Tenira, August — September 1918 (P. Rotrou).
86 Novitates Zooloqicae XXVTI. 1920.
332. Eublemma purpurina (Schiff. & Den.).
Phalaena -purpurina Schifferniuller and Denis, Ank. Syst. Werk. Schmett. Wienergeg. p. 88 (1775)
(Vienna).
I have 9 Mauretanian specimens: 2 <$<$ Ain Draham, September 1911
(V. Faroult); 1 $ Khenchela, May 1912 (W. R. and K. J.); 2 $$, 4 $$ El
Mahouna, June 1919 (V. Faroult).
The 2 Am Draham $$ are ab. secunda Stdgr. with the mauve-lilac colouring
reduced to a patch at the apex of forewing.
333. Eublemma candidana (Fabr.).
Pyralis candidana Fabricius, Entom. Syst. vol. iii. pt. ii. p. 245. No. 11 (1794) (Montpellier).
1 ? Sidi Ferruch, July 1911 (A. Thery).
334. Azenia sabulosa (Rothsch.).
Eublemma sabulosa Rothschild, Novit. Zool. vol. xx. p. 127. No. 64 (1913) (South Oued Mya).
The type and a second $ so far are all that have been recorded.
1 $ South Oued Mya, May 1912 (Hartert and Hilgert) ; 1 $ Amgid, February
1914 (Geyr von Schweppenburg).
335. Synthymia fixa australis (Oberth.).
Meloptria monngramma australis Oberthiir, Etud. Lipid. Comp. fasc. xvi. p. 199. pi. xdvii. f. 4137
(1919) (Geryville).
I have a very poor series of this handsome species.
5 <3<3, 5 $$ from Sidi-bel-Abbes, June 1917 (M. Rotrou) ; Masser Mines,
Moroccan Frontier May 1914, Oued Hamidou June 1912 (V. Faroult) ; Foret de
Tenira, June 1918 (P. Rotrou).
336. Eriopus latreillei (Dup.).
Noclua latreillei Duponchel, Lepid. France, vol. vii. Noct. vol. iv. pt. 1. p. 327. pi. 120. f. 2 (1827)
(Provence).
Our Mauretanian series is very scanty : 13 specimens from Guelt-es-Stel
October 1913, Ain Sefra July 1915, Masser Mines June 1914, Bou Saada March
— May 1912, Metlili north of Laghouat September 1917, Ain Draham September
1911 (V. Faroult) ; Sebdou, July 1918 (P. Rotrou).
337. Eriopus juventina (Cram.).
Phalacna juventina Cramer, Pap. Exoi. vol. iv. pt. xxxiv. p. 245. pi. cecc. i. N. (1782) (Surinam ! !).
Of this elegant species I have only 6 examples, 5 from Tunisia. I believe
this is the first record for Mauretania.
All 6 specimens (4 <$<3, 2 $$) are very pale, and the ground-colour some-
what rufous, but as they are rather worn, it is not possible to say if the North
African examples belong to a separate subspecies.
3 cJcJ, 2 ?$ Ain Draham, Tunisia, September 1911, 1 <2 Oued Hamidou, June
1912 (V. Faroult).
Novitates Zoolooicaz XXVII. 1920. 87
338. Phlogophora adulatrix (Hiibn.).
Noctua adulatrix Hiibner, Samml. Europ. Schmelt. Noct. S. 517, 649, 650 (1818).
Of this conspicuous insect the series at Tring from Mauretania consists of
161 specimens from Hammam R'hira, May 1908-1911 (W. R., E. H., and K. J.,
and Faroult) ; Environs d'Alger, May 1908 (W. R., K. J., and Dr. Nissen) ;
Biskra, March 1908 (W. R. and E. H.) ; Hammam Meskoutine, May 1914 (W. R.,
E. H., and K. J.) ; Sidi-bel-Abbes, August-September 1917 (M. Rotrou) ; Am
Draham September 1911, Environs de Setif 1911, El Kantara August 1917, Oued
Hamidou June 1912, El Hamel May 1912, Bou Saada and Djebel Kerdada May
1912, Masser Mines June 1914 (V. Faroult); Guelt-es-Stel, May— October 1912-1913
(V. Faroult) ; Sebdou, Foret de Tenira, May— June 1918 (P. Rotrou).
The British Museum lias 1 $ Hammam-es-Salahin, April 1904, Lord
Walsingham.
339. Phytometra orichalcea (Fabr.).
Noctua oricluilcea Fabricius, Syst. Entom. p. 607. No. 70 (1775) (India).
Noctua aurifera Hubner, Samml. Eur. Schmelt. Noct. f. 463 (1822).
Mr. Oberthiir adopts Hiibner's name for this species, as lie figures it, but even
under his system in regard to figures he ought to have adopted Martyn's name of
chrysitina of twenty-five years' earlier date, as he gives a good figure in Psyche ;
perhaps however Mr. Oberthiir, like many other people, adopts the very legitimate
doubt as to Martyn's Psyche having been properly published.
We have 34 Mauretanian specimens at Tring from Mazagan, Morocco, July
1900 (W. Riggenbach) ; Sidi-bel-Abbes, July— August 1916-1917 (M. Rotrou) ;
Oran, April 1913 (W. R. and E. H.) ; Environs de Setif, 1911 (V. Faroult) ; En-
virons d'Alger (Dr. Nissen).
Mr. Oberthiir appears to have only one record of this species from Batna.
340. Phytometra chalcytes (Esp.).
Noctua chalcytes Esper., Schmelt. vol. iv. pt. ii. p. 447. No. 167. pi. cxli. f. 3 (1789) (Italy).
Here also Mr. Oberthiir only seems to have one record, Lambessa.
The Mauretanian series at Tring consists of 72 examples from Sidi-bel-Abbes,
Messer, June — September 1916-1917 (M. Rotrou) ; Hammam R'hira September
1916, Le Tlelat October 1915, Batna October 1910 (V. Faroult) ; Environs
d'Alger (Dr. Nissen) ; Mazagan, Morocco, July 1900 (W. Riggenbach).
341. Phytometra daubei (Boisd).
Plusia dauhei Boisduval, Gen. et Ind. Meth. p. 159. No. 1281 (1840) (S. France).
The Mauretanian examples at Tring number 13 from Biskra, March — April
1908-1911 (W. R, and E. H.) ; Sidi-bel-Abbes, September 1917 (M. Rotrou);
Bordj-ben-Aneridj November 1911, Bou Saada March 1912, Lalla Marnia
November 1914, El Kantara, September 1917 (V. Faroult).
342. Phytometra accentifera (Lef.).
Plusia accentifera Lefebre, Ann. Soc. Linn. Paris. 1827. p. 94. pi. 5. (I. 1, 2.
Of this species I have 4 Algerian specimens : 1 Batna (A. Nelva) ; 3 Sidi-
bel-Abbes, September 1916-1917 (M. Rotrou).
Mr. Oberthiir has no record of this species.
88 Novitates Zoolooicae XXVII. 1920.
343. Phytometra intermixta Warr.
Phytomelra intermixta Warren in Seitz, Grossschmett. Erde, vol. iii. p. 357. pi. 6ig. (1913) (Pu-Tsu-Fu.
\V. China).
This species has always been mixed up with orichalcea.
3 Mazagan, Morocco, July 1900 (W. Riggenbach).
344. Phytometra ni (Hiibn).
Noclua ni Hiibner, Samml. Eur. Schmett. Xoct. f. 2S4 (1802).
Of this species we have 149 Mauretanian specimens at Tring.
I had at one time decided that there were two forms of this species in Algeria,
the typical form on the coast and in the Tell and a paler desert form elsewhere,
but 1 find light and dark specimens from the same locality now that I have a
good series.
The 149 examples are from Sebdou, June 1918 (P. Rotrou) ; Les Pins,
Environs de Taourirt, July 1918 (M. Rotrou) ; Blida November 1915, Aflou
October 1916 (V. Faroult) ; Amgid, Ain Tahart, Oued Amra February — March
1914 (Geyr von Schweppenburg) ; Biskra, March — April 1908-1909 (W. R. and
E. H.) ; Mazagan, Morocco, July 1900 (W. Riggenbach); Environs d'Alger
(Captain Holl) ; Hammam R'hira May 1908-1916 (W. R., E. H., and K. J.,
and Faroult) ; Ain Sefra, May— July 1913-1915 (W. R. and E. H., and
Faroult) ; Colomb-Bechar March — April 1912, Perregaux September 1915,
Oudida May 1914, Lalla Marnia April 1914, Djebel Kerdada and Bou Saada
May 1912, Bir Stil March 1917, El Kantara August 1917, Oued Hamidou June
1912, El Hamel May 1912, north side of Djebel Zaccar Miliana August 1916 (V.
Faroult) ; Sidi-bel- Abbes, May— September 1915-1917 (M. Rotrou) ; Oran,
April 1913 (W. R. and E. H.) ; Guelt-es-Stel, April— May 1912-1913 (W. R.
and K. J., and Faroult) ; Oued Nca April 1914, El Golea March 1912 (Hartert
and Hilgert) ; Batna (A. Nelva) ; Hammam Meskoutine, May 1914 (W. R.
and K. J.) ; Belvedere, Tunis, August — September 1915 (M. Blanc) ; Ain Draham,
September 1911 (V. Faroult).
345. Phytometra gamma (Linn.).
Phalaena gamma Linnaeus, Syst. Nat. edit. x. p. 513. No. 91 (1758) (Sweden).
This almost world-wide species is just as abundant in Algeria as elsewhere.
I have not kept nearly all that have come to hand between the years 1908 and
1919, during which I have been amassing Algerian material.
The series retained at Tring from Mauretania consists of 268 examples from
Mazagan, Morocco, January — July 1901-1903 (W. Riggenbach) ; Blida les
Glacieres, June 1908 (W. R. and K. J.) ; Biskra January— May 1908-1914,
Tlemcen April 1913, Oran April 1913 (W. R. and E. H.) ; Environs de Batna,
1909-1912 (A. Nelva) ; Lambessa, July 1914 (A. Nelva) ; Environs d'Alger, May
1911 (W. R. and E. H.) ; Hammam R'hira, February— May 1908-1918 (W. R.,
E. H., and K. J., and Faroult) ; Sidi-bel-Abbes, Ain Fezza, Les Pins, July —
September 1916-1918 (M. Rotrou) ; Khenchela May 1912, Souk Ahras April
1914, Hammam Meskoutine May 1914 (W. R. and K. J.) ; Guelt-es-Stel, April-
October 1912-1913 (W. R. and K. J., and Faroult) ; Perregaux October 1915,
NOVTTATES ZOOLOGICAE XXVII. 1920. 89
Oued Hamidou June 1912, Bordj-ben-Aneridj November 1911, Lalla Marnia
April — May 1914, Blida February 1916, Nedroma May 1914, Masser Mines May
1914, Mecheria June 1918, Ai'n Draham August — September 1911, Bou Saada
March— May 1911-1912, Tilghemt April 1912, Boghar May 1912 (V. Faroult) ;
Sebdou, May 1918 (P. Rotrou) ; Slassel Danoun, December 1913 (Geyr von
Sen weppenburg) .
In British Museum are 1 $ Hammam-es-Salahin April 1904, 1 $ Tkout, April
1906, Lord Walsingham ; 1 cJ, 1 ? Hammam Meskoutine, April 1913, P. A. Buxton ;
1 c? Tangier, Leech coll.
[Protomeceras mimicaria (Oberth.).
Cimelia mimicaria Oberthiir, Bull. Soc. Entom. France, 1887. p. 58 (Sebdou).
In spite of the continued doubts evinced by Mr. Oberthiir as to the exact
classificatory position of this very remarkable insect, I think there can be no
doubt that its correct position is next to Synthimia and in front of Megalodes
towards the end of the subfamily Zenobiinae (Acronyctinae).
I have never received this insect.]
346. Scoliopteryx libatrix (Linn.).
Phaktena libatrix Linnaeus, Syst. Nat. edit. x. p. 507. No. 54 (1758) (Sweden).
I have only had three Mauretanian examples : 1 <J, 1 $ Sidi-bel-Abbes, Sep-
tember 1917 (M. Rotrou) ; 1 $ El Mahouna, June 1919 (V. Faroult).
347. Amphipyra pyramidea (Linn.).
Phalaena pyramidea Linnaeus, Syst. Nat. edit. x. p. 518. No. 119 (1758).
I have just one dozen Mauretanian examples : from Blida les Glacieres
June 1908 (W. R. and K. J.) ; Batna (A. Nelva) ; Ain Draham September 1911,
Hammam R'hira July 1917 (V. Faroult) ; Sidi-bel-Abbes, July— August 1917
(M. Rotrou).
These all belong to the large and fine form ab. variegata Warr. ; if this form is
proved to be constant in Algeria and Tunis it would have to stand as a distinct
subspecies —
Amphipyra pyramidea variegata Warr.
Amphipyra pyramidea ab. variegata Warren in Seitz, Grossschmett. Erde, vol. iii. p. 158. pi. 386-
(1911) (Algeria).
348. Pyrois effusa (Boisd.).
Amphipyra effusa Boisduval, Eur. Lepid. Ind. Meth. p. 68 (1829) (Sicily).
This insect is widely distributed in Algeria, being found far into the interior
and also along the coast, though at Tring we have only examples from the Tell
regions.
24 specimens from Hammam R'hira, May— June 1911-1916 (W. R. and
E. H, and Faroult) ; Blida les Glacieres, June 1908 (W. R. and K. J.) ; Hammam
Meskoutine, May 1909-1914 (W. R., E. H., and K. J.) ; El Mahouna, June 1919
(V. Faroult).
90 NOVITATES ZOOLOGICAE XXVII. 1920.
349. Amphipyra tetra (Fabr.).
Noctua tetra Fabricius, Manl. Ins. vol. ii. p. 138. No. 31 (1787) (Austria).
Of this species the Tring Museum possesses a very poor Mauretanian series :
7 specimens from Guelt-es-Stel October 1913, Ai'n Sefra July 1915 (V. Faroult).
350. Amphipyra tragopoginis distincta subsp. nov.
$. This insect is a very distinct subspecies of tragopoginis Linn., being larger
and more brightly coloured.
Head and thorax deep black-brown ; abdomen smoky wood-brown ; palpi
and antennae black. Forewings basal three-fourths deep black -brown, powdered
with dark grey, orbicular represented by a black spot or streak and reniform
by two black spots ; outer one-fourth sooty blackish grey. Hindwings rusty
wood-brown washed with sooty grey.
Length of forewing, 20 mm ; expanse, 47 mm.
1 $ north side of Djebel Zaccar, nr. Miliana August 1916, 1 $ Hammam
R'hira May 1917 (V. Faroult).
Mr. Oberthiir does not record tragopoginis.
351. Mania maura (Linn.).
Phalaena maura Linnaeus. Syst. Nat. edit. x. p. 512. No. 88 (175S) (Mauretania).
The series from Mauretania at Tring consists of 82 specimens from Batna
(A. Nelva) ; Guelt-es-Stel August 1913, north side of Djebel Zaccar, nr. Miliana
August 1916, Ai'n Draham July 1911 (V. Faroult) ; Hammam R'hira, May — June
1913-1916 (W. R. and E. H, and Faroult) ; Sebdou, Foret de Tenira, September
1918 (P. Rotrou) ; Sidi-bel-Abbes, July 1917 (M. Rotrou) ; Lambessa 1912 (A.
Nelva).
352. Apopestes spectrum maura Warr.
Apopestes spectrum maura Warren in Seitz, Grosssehmett. Erde, p. 370. pi. 686. (1913) (Algeria).
The name maura could not be used for this insect before the genus was split
in two, as it is antedated twenty-five years by Staudinger's maura, a species near
catapfianes, described by its author as a subspecies of cakiphanes, but is quite in
order now.
This is not a very distinct subspecies of spectrum, but it appears fairly
constant, the lines being less diffuse and narrower.
The Tring series comprises 64 specimens from Batna (A. Nelva) ; El Kantara,
March 1908-1911 (W. R. and E. H.) ; Mazagan, Morocco, July 1901 (W. Riggen-
bach) ; Leila Kredidja, Tala Rana, Kabylie, July 1907-1908 (Dr. Nissen) ; Foret
de Tenira, Sebdou, September 1918 (P. Rotrou) ; Sidi-bel-Abbes July 1917, Les
Pins August 1918 (M. Rotrou) ; Guelt-es-Stel, April— October 1912-1913 (W. ft
and K. J., and Faroult) ; Perregaux October 1915, Aflou October 1916 (V.
Faroult) ; Am Sefra, May— June 1913-1915 (W. R. and E. H., and Faroult) ;
Bordj-ben-Aneridj October 1912, Medjes October 1912, north side of Djebel
Zaccar, nr. Miliana August 1916 (V. Faroult).
N0V1TATES ZOOLOGICAE XXVII. 1920. 91
353. Autophila maura (Stdgr.).
Spintherops catapkanes var. maura, Staudinger, Slett. Enlom. Zeit. vol. 49. p. 63 (1888) (Lambessa).
Spintherops roseata Rothschild, Novit. Zool. vol. xix. p. 126. No. 6 (1912) (Ghardata).
One would not look generally for the description of an Algerian moth in an
article dealing with Asiatic species, so I unfortunately redescribed the present
species.
Mr. Oberthur as well as Staudinger and most other authors have placed
this insect under cataphanes Hiibn. as a race or variety, but Sir George Hampson
is convinced that it and several other forms placed under cataphunes are distinct
species.
The series at Tring numbers 78 specimens from Biskra, March — April 1908-
1909 (W. R. and E. H.) ; Guelt-es-Stel July— October 1913, Ain Sefra May
1915, Ras Chergui July 1915, Colomb Bechar March— April 1912, Msila May 1915,
Bordj Chegga March 1917, Tilghemt April 1912, Laghouat March 1912, Bou
Saada April — May 1911-1912 (V. Faroult) ; El Kantara March — August 1911-
1917 (V. Faroult); El Kantara March— August 1911-1917 (W. R. and E. H.,
and Faroult) ; Sebdou, June — July 1918 (P. Rotrou) ; Oued Abbou, January
1914 (Geyr von Schweppenburg) ; Ghardaia, April 1911 (W. R. and E. H.)
(including type of roseata) ; north of Ain Guettera, Ain Guettera, South Oued
Mya, In-Salah Tidikelt Oases, Fort Miribel, north of El Golea April— May 1912,
Oued Nca April 191-1 (Hartert and Hilgert).
The British Museum has 1 $ Algeria, Mrs. Nicholl ; 2 <$£, 7 <j*j> Hammam-
es-Salahin, March — May 1903-1904, Lord Walsingham.
354. Autophila ligaminosa (Eversm.).
Spintherops ligaminosa Eversniann, Bull. Soc. Imp. Nat. Mosc. 1851. p. 630 (Georgia and Armenia).
This was taken by Mr. Oberthur to be typical cataphunes. Sir George
Hampson considers it a distinct species.
6 cfcj, 9 $$ Sebdou, August 1918 (P. Rotrou) ; 1 ? Environs de Batna (Nelva) ;
1 $ Sidi-bel-Abbes, June 1916 (M. Rotrou) ; 1 <J Hammam R'hira, February 1918.
Mr. Oberthur does not record this species, having in error put it down as
cataphanes.
355. Autophila dilucida libanotica (Stdgr.).
Apopestes dilucida v. ? libanotica Staudinger, Cat. Lepid. Palaear. Faun. edit. iii. p. 251. No. 2723c
(1901) (Lebanon).
Staudinger, Mr. Oberthur, and most other entomologists have identified
this insect as dilucida dilucida Hiibn., but I consider it agrees best with the sub-
species libanotica Stdgr.
In the Stett. Entom. Zeit. vol. xlix. p. 63 (1888) (Biskra) Dr. Staudinger
separated a more rosy red Autophila as Spintherops dilucida var. rosea, and hitherto
everyone has followed him without carefully examining a series of this very
common insect. I was first struck by the longer and narrower wings of rosea,
and then I found that I had both rosea and dilucida libanotica from Guelt-es-Stel
and no specimens showing any intermediate characters.
I at once got Rr. Jordan to examine the <$ genital armature, and we found
that this differed in the two insects. I then looked up my non-Mauretanian
92 NOVTTATES ZOOLOGICAE XXVII. 1920.
material and perceived at once that there was a much greater resemblance
between rosea Stdgr. and cerealis Stdgr. than between rosea and the forms of dilu-
cida. Dr. Jordan on examining the genital armature of cerealis found that it
really agreed with that of rosea. Therefore rosea is a subspecies of cerealis and
not of dilucida, and must stand as Autophila cerealis rosea Stdgr.
We have at Tring 102 Algerian examples of dilucida libanotica Stdgr. from
El Kantara, March— April 1908-1911 (W. R. and E. H., and Faroult) ; Batna,
June 1909-1914 (A. Nelva) ; Guelt-es-Stel, May— June 1913 (V. Faroult) ;
Djebel Chelia, June 1911 (V. Faroult) ; Environs d'Alger (Captain Holl) ; Sidi-
bel-Abbes, June 1915-1917 (M. Eotrou) ; Bou Saada May 1912, Oued Hamidou
June 1912 (V. Faroult) ; Hammam R'hira, May— June 1913-1917 (W. R. and
E. H., and Faroult) ; Masser Mines, June 1914 (V. Faroult).
The British Museum has 1 <$ Algeria, Mrs. Nicholl.
356. Autophila cerealis rosea (Stdgr.).
Spintherops dilucida var. rosea Staudinger, Stett. Entom. Zeit. vol. 49. p. 63 (18S8) (Biskra).
As the genital armature of the (J of this insect differs from that of dilucida
and agrees with that of cerealis Stdgr., it proves rosea to be a distinct species from
dilucida and that it is a subspecies of cerealis.
We have at Tring 333 specimens of this species from Biskra, March 1908
(W. R. and E. H.) ; Gafsa and Biskra (Staudinger) ; El Hamel May 1912, Mograr
Foukani November 1916, Guelt-es-Stel May 1913, Bou Saada May 1912, Laghouat
March 1912, Tilghemt April 1912 (V. Faroult) ; Oued Nca April 1914, South
Oued Mya, north of Ain Guettera, El Golea, April — May 1912 (Hartert and
Hilgert) ; Oued Abbou January 1914, south of Ouargla December 1913 (Geyr
von Schweppenburg) ; Ain Sefra, May 1913-1915 (W. R and E. H., and Faroult).
The British Museum has 1 <$ Mauretania. Staudinger and Bang-Haas ; 1 §
Biskra, February 1894, A. E. Eaton ; 2 $? Hammam-es-Salahin, February 1894,
Lord Walsingham ; 1 <$ Hammam Meskoutine, March 1911, Meade- Waldo ; 1 $
Sbietla, Tunisia 1913, G. C. Champion.
357. Tathorhynchus exsiccata (Led.).
Spinlherops exsiccata Lederer, Verh. Zool. Bot. Ver. Wien, vol. v. p. 204. pi. 2. f. 12 (1855) (Beirut).
This species is by no means numerous in Algeria.
I have only received 15: 5 Guelt-es-Stel, April— May 1912-1913 (W. R.
and E. H., and Faroult) ; 3 Ain Sefra July 1915, 1 Bou Saada May 1912 (V.
Faroult) ; 3 Sidi-bel-Abbes, June 1917 (M. Rotrou) ; 2 Amgid February, 1 Oued
Ag'elil March 1914 (Geyr von Schweppenburg).
358. Anthracia ephialtes (Hiibn).
Nortua ephialtes Hiibner, Samml. Eur. Schmmett. Noel. i. 652 (1822).
Of this species I have only 8 specimens from Algeria.
7 $? Sidi-bel-Abbes, September 1917 (M. Rotrou) ; 1 $ Sebdou, September
1918 (P. Rotrou).
The British Museum has 1 (J, 1 $ Morocco, Meade- Waldo.
NOV1TATES ZOOLOQICAE XXVII. 1920. 93
359. Pandesma anysa distincta subsp. nov.
cj$. Differ from anysa anysa in being smaller, less stoutly built, and more
uniform deep grey in colour.
Length of forewing: <J a. anysa 22 mm., a. distincta 15 mm.
Length of forewing : $ a. anysa 24 mm., a. distincta 18 mm.
Expanse : a. anysa <$ 51 mm., $ 55 mm. ; a. distincta <J 36 mm., $ 42 mm.
1 cJ, 1 $ Sidi-bel-Abbes, September 1917 (M. Rotrou) ; 1 ? Belvedere, Tunis
(M. Blanc) ; 2 &J Ain Sefra, July 1915 (V. Faroult).
Mr. Oberthur pointed out the difference from anysa anysa, but did not name
the form, though he figures it.
360. Pandesma anysa sennaarensis Feld. & Rog.
Pandesma sennaarensis Felder and Rogenhofer, Reise der Novara, Zoology, vol. ii. sect. 2. pi. cxi. and
Tafel-Erkl. f. 26 (1872) (Cape Colony and Sennaar).
This form occurs in the interior of the Sahara ; the $<$ are much whiter
and the $$ paler and less pure grey.
4 (JcJ, 5 $$ Amgid, Oued Ag'elil, I-n-Kelemet, Oued Amra, February — March
1914 (Geyr von Schweppenburg). I identified this in 1915 as a. terregena Christ.,
but it agrees best with Felder's form.
Mr. Oberthur does not record this.
361. Cortyta acrosticta (Piingl.).
Pericyma acrosticta Piingler, Iris, vol. xvi. p. 290. pi. vi. f. 6 (1903) (Engeddi, Dead Sea).
This is quite distinct from vetusta, under which Sir George Hampson has placed
it as an aberration.
1 (J Ti-n-tabarik, April 1914 (Geyr von Schweppenburg).
This is also not recorded by Mr. Oberthur.
362. Cortyta rosacea (Rebel). (PL XVI. f. 17.)
Pericyma rosacea Rebel, Denkschr. Math. -Nat. Akad. Wissensch. vol. lxxi. p. 60 (1907) (Socotra).
I have a fine series of this very rare insect from the Algerian Sahara ; it does
not vary except in size.
1 $ South Oued Mya, April 1912 (Hartert and Hilgert) ; 19 <J<J, 6 ?$ Oued
Dehin, Amgid, Rharis, Aceksem, Oued Gif-Aman, Oued Tamoudat, Oued Ag'elil,
north of Ideles, February — April 1914 (Geyr von Schweppenburg).
Mr. Oberthur does not record this.
363. Cortyta leucoptera (Hmpsn.).
Hypaelra leucoptera Hampson, Proc. Zool. Soc. Land. 1896, p. 264. pi. x. f. 1 (Aden).
Pericyma dispar Piingler, Iris, vol. xvi. p. 290. pi. v. ff. 7, la (1903) (Engeddi, Dead Sea).
Pericyma fasciolala Warren, Novit. Zool. vol. xii. p. 24. pi. iv. ff. 11, 21 (1905) (Nakheila, Egypt.
Sudan).
Polydesma halnearia Distant, Ann. Mag. Nat. Hist. (7) I. p. 228 (1898) (Waterburg, Transvaal).
Cortyta impar Hampson, Cat. Lepid. Phal. Brit. Mus. vol. xiii. p. 317. No. 8129. pi. ccxxxii. f. 21
(1913) (Punjab).
Homoptera eremochroa Hampson, Journ. Bomh. Nat. Hist. Soc. vol. xxi. p. 1222 (1912) (Deesa, Bombay).
In the British Museum Catalogue of Moths Sir George Hampson has all the
above 6 insects as separate species, but since the publication of vol. xiii. of the
94 Novitates Zoolooicae XXVII. 1920.
above Catalogue, two very remarkable series of specimens have come to hand,
first a series of 1 8 specimens from the Algerian Sahara sent me by Herr Geyr von
Schweppenburg in 1914, and secondly a very large series received by Professor
Poulton from Mr. Feather collected in Somaliland. In these two series every
intergradation between the 6 insects named above is represented, proving them
all to belong to a single protean species with an extraordinary range of variation.
Unfortunately leucoptera Hampson, as the oldest name, has to be used for the species,
for the very white form to which it was originally given appears to be the rarest ;
in my series of 21 Algerian specimens, only the <$ from Colomb-Bechar is of this
form.
1 <J Colomb-Bechar, March— April 1912 (V. Faroult) ; 5 ££, 13 $$ Amgid,
Oued Pehir, Oued Gif-Aman, Oued Tamoudat, Oued Amra, Rharis. Am Tahart,
February — April 1914 (Geyr von Schweppenburg) ; 2 $$ South Oued Mya, and
north of Ain Guettera, April 1912 (Hartert and Hilgert).
The last two are type and cotype of fasciolata subsimilis Warren, but are only
further aberrations of leucoptera, as is my Cortyta pungleri.
This is also not recorded by Mr. Oberthiir.
364. Hypoglaucitis benenotata moses Stdgr.
Hypoglaucitis moses Staudinger, Iris, vol. vii. p. 284. pi. 9. f. 17 (1894) (Egypt [Cairo? ]).
Of the 6 o;J, 6 ?$ from Algeria at Tring, 2 ,$<$ are typical moses, 1 <J is too
worn to be sure of, and 3 <$<$ are ab. ochrea Warr. Of the 6 $$, 5 are ab. ochrea
and 1 typical moses. 4 (JcJ, 3 $$ South Oued Mya, April 1912 (Hartert and
Hilgert) ; Laghouat March 1912, Nedrorna and Lalla Marnia May 1914 (V.
Faroult) ; 1 $ Aceksem, 1 $ Tahihout, April — May 1914 (Geyr von Schweppen-
burg).
Not recorded by Mr. Oberthiir.
365. Mageutica alchymista alchymista (Schiff. & Den.).
Phalaena alchymista Schiffenniiller and Denis, Ank. Syst, Werk. Schmett. Wienergeg. p. 89 (1775)
(Vienna).
Of typical alchymista I only have 3 specimens: 1 Hammam R'hira, June 1917
(V. Faroult) ; 2 Batna (A. Nelva).
Of ab. varia I have 1 $ from Batna (A. Nelva).
The British Museum has 1 <J, 1 $ Batna, Staudinger and Bang-Haas.
366. Mageutica alchymista uniformis (B.-H.).
Catephia alchymista var. uniformis Bang-Haas, Iris, vol. xxiv. p. 41 (1910) (Ain Draham).
This form is not found in Europe, and in Eastern Algeria and Tunisia at
least 95 per cent, of the individuals belong to it, so 1 consider it a good subspecies.
(I have placed the form varia as an aberration under a. alchymista, but 1 am
doubtful as to its status. Mr. Oberthiir says it is the prevailing form at
Lambessa, but I have only 3 Batna examples, 2 being typical alchymista and 1
varia. My material is useless for decision, being so poor in numbers.)
Of a. uniformis we have at Tring 67 specimens from Ain Draham July —
August 1911, Environs de Setif 1911 (V. Faroult).
Of these 67 examples 4 are intermediate between uniformis and alchymista.
XOVITATES ZOOLOOICAE XXVII. 1920. 95
367. Catephia leucomelas (Linn).
Phalaena leucomelas Linnaeus, Syst. Nat. edit. x. p. 518. No. 121 (1758) (Europe).
Mr. Oberthiir makes use of Rambur's name, which is 71 years later than
Linnaeus's, although the latter's leucomelas is figured in Clerck's Icones.
We have 7 Mauretanian examples : 4 Environs d'Alger, May — June 1908
(W. R. and K. J., and Dr. Nissen) ; 3 Hammam R'hira, July 1917 (V. Faroult).
368. Anumeta atrosignata harterti Rothsch.
Anumeta henkei Itarterti Rothschild, Novit. Zool. vol. si. p. 469 (1913) (El Golea).
This unfortunate insect has been banded about from pillar to post by Sir
George Hampson, Mr. Warren, Mr. Oberthiir, and myself. It lias been called
henkei Stdgr., spilota Ersch., henkei harterti Rothsch., and atrosignata Walk.
The truth is that spilota Ersch., harterti Rothsch., and atrosignata Walk, are 3
subspecies of one widely-spread desert species.
The Tring Museum has 16 specimens: 2 <J(J, 1 $ El Golea, 1 <J, 1 $ San-
dana, south of Ghardaia, May 1912 (Hartert and Hilgert) ; 2 <$<$ Bordj Mgeitla,
April 1909 (W. R. and E. H.) ; 4 <?<?, * $$ Amgid, Aceksem, Tahihout, Oued
Dehin, Ain Tahart, February — April 1914 (Geyr von Schweppenburg) ; 1 Colomb-
Bechar, March— April 1912 (V. Faroult).
369. Anumeta sabulosa Rothsch. (PI. XVI. f. 15.)
Anumeta sabulosa Rothschild, Novit. Zool. vol. xx. p. 129. No. 78 (1913) (South Oued Mya).
Of this very distinct species we have 1 1 examples at Tring from South Oued
Mya, May 1912 (Hartert and Hilgert) ; Amgid, Oued Dehin, Ain Tahaut, February
— April 1914 (Geyr von Schweppenburg).
The type was unfortunately recorded in the original description as a <J ; it
is in reality a <j>.
370. Anumeta spatzi Rothsch. (PI. XVI. ff. 11, 12.)
Anumeta spatzi Rothschild, Ann. Mag. Nat. Hist. (8) xvi. p. 257. No. 51 (1915) (Amgid).
Of this fine species the Tring series contains 11 specimens from Amgid,
Tahihout, Ain Taiba, April — May 1914 (Geyr von Schweppenburg).
371. Anumeta major Rothsch. (PI. XVI. ff. 13, 14.)
Anumeta major Rothschild, Novit. Zool. vol. xx. p. 130. No. 79 (1913) (N. of El Golea).
In my article on Herr Geyr von Schweppenburg's collection (see above) I
recorded 2 <$<$ and 1 $ as being major. On closer examination I find all 3 speci-
mens from Ain Taiba are $3.
1 ? north of El Golea, May 1912 (Hartert and Hilgert) ; 3 <J<J Ain Taiba,
May 1914 (Geyr von Schweppenburg).
The most striking difference at first sight between spatzi and major is that the
black spot in the hindwing is free in the white patch in major, while in spatzi it
coalesces with the brown shadow band. This is the insect Warren described as
harterti while figuring the real harterti.
96 Novitates Zoolooicae XXVII. 1920.
[Anumeta cestis cestis (Menet.).
Catephia cestis Menetries Mem. Acad. Imp. St. Pet. Scien. Nat. vol. vi. Descr. Ins. Iiec. feu Lehmann,
p. 74. No. 870. pi. vi. f. 10 (1848) (Bachkirie).
This is a pure desert-loving insect, and where we caught it in 1909 in the
Oued Souf region it was taken among the sand-dunes.
The series from Algeria when contrasted with my series from Central Asia
appears less robust, and the pattern of the forewings, when the whole of each
series is compared with the whole of the other series, gives a different impression ;
but the real difference lies in the dark patches in the hindwing, which are very
heavy and generally confluent in cestis cestis and smaller and generally separated
into three in the Algerian race.
Of cestis cestis the Tring Museum has 25 examples, of which 4 are ab. punctata
Men. and 5 ab. uniformis Warr.]
372. Anumeta cestis parvimacula subsp. nov.
^ 5- Differ from cestis cestis in being less robust and in the black markings
on the hindwings being smaller in extent and generally broken up.
65 specimens, of which 10 are ab. uniformis Warr., from Bordj Ferdjan Bordj
Mgeitla, Bordj Mecht-el-Kaid, April 1909 (W. R. and E. H.) ; Arefidji, halfway
between Ouargla and El Golea, north of El Golea, Hassi el Hadjar, Hassi Dinar,
March 1912 (Hartert and Hilgert) ; Tilghemt April, Bou Saada May 1912 (V.
Faroult).
373. Anumeta hilgerti (Rothsch.).
Palpangula hilgerti Rothschild, Entom. Zeit. Stuttgart, vol. xxiii. p. 142 (1909) (Bordj Ferdjan).
The series at Tring contains 34 examples, of which 3 are ab. brunnea Warr.
from Amgid, Oued Dehir, Temassinin, Oued Gif-Aman, Ain Taiba, Oued Amra,
and north of Ideles, January — May 1914 (Geyr von Schweppenburg) ; Oued
Abiod, Hassi el Hadjar, El Golea, halfway between Ouargla and El Golea,
Arefidji, March — May 1912 (Hartert and Hilgert) ; Colomb Bechar, March —
April 1912 (V. Faroult) ; Bordj Ferdjan, Bordj Mgeitla, April 1909 (W. R. and
E. H.).
[At the end of the paragraph on Palpangula harterti Mr. Oberthiir mentions
Anumeta sabulosa, stating it was described by Warren in Seitz, but that as it was
not figured it was a " nomen nudum." This is Mr. Oberthiir's usual proceeding,
but as he goes so far as to tell his readers that such a creature had been
described, he might at least have given the author's name correctly. Anumeta
sabulosa was described by me, and therefore the author of the name is Rothschild
not Warren. As to the question of the authenticity of a name depending on a
good figure, I maintain that far oftener a good description is more easily recog-
nised than even a good figure ; especially as the figure only represents one speci-
men and not a whole series, and in nine times out of ten represents the peculiari-
ties which struck the artist's eye, while the differentiating characters may not be
those emphasised in the drawing.
In addition the International Rules of Nomenclature nowhere insist on
anything more than a fairly accurate and consequently recognisable description,
Novitates Zoolooioae XXVTI. *1920. 97
and therefore Mr. Oberthiir and his friends who support him in his view about
figures are not in accord with the general body of zoological opinion all over
the world.]
374. Anydrophila sabourodi (D. Luc).
Palpangula sabourodi Daniel Lucas, Bull. Soc. Enlom. France, 1907. p. 180 (Zarcine, Tunisia).
Mr. Oberthiir as well as the author place this species in Palpangula = Anu-
meta. This is quite wrong as sabourodi, and the 4 Central Asian species which
form the genus Anydrophila are Catocalinae, whereas Anumeta {Palpangula) is a
genus of Noctuinae separated by two families from the Catocalinae.
We have the other 4 only recorded specimens, beyond the type, at Tring.
2 £<$ Oued Nca, April 1914 (Hartert and Hilgert) ; 1 ^ Aceksem, April 1914
(Geyr von Schweppenburg) ; 1 $ A'in Sefra, June 1915 (V. Faroult).
« 375. Anumeta straminea (B.-H.).
Palpangula straminea Bang-Haas, Iris, vol. six. p. 135. pi. v. f. 11 (1906) (Gafsa, Tunisia).
Of this characteristic species we have at Tring a large series ; but curiously
enough, although Mr. Oberthiir says it is common at Biskra, we only obtained
two specimens there during our four prolonged visits. 347 specimens from Colomb
Bechar March— April 1912, Bou Saada March— May 1912 (V. Faroult) ; Nza-
ben-Rzig, Mraier, Tamerna, half-way between Touggourt and Ouargla, Arefklji,
Hassi el Hadjar, north of El Golea, halfway between Ouargla and El Golea
February — May 1912 (Hartert and Hilgert) ; south of Bledet-Ahmar, south of
Ouargla, Slassel Dhanoun, Hassi Abbou, Oued Abbou, Timassinin, I-n-Kelemet,
Amgid, December 1913 — February 1914 (Geyr von Schweppenburg) ; Biskra
February 1908-1911, Bordj Ferdjan, Bordj Mgeitla April 1909 (W. R. and E. H.) ;
Tunis (Staudinger).
The British Museum has 2 $$ Hammam-es-Salahin, March 1904, Lord
Walsingham ; 1 <J, 2 $$ Colomb-Bechar, February 1912, V. Faroult ex Tring
Museum.
376. Leucanitis kabylaria B.-H.
Leucanilis kabylaria Bang-Haas, Iris, vol. six. p. 136. pi. v. f. 7 (1906) (Gafsa, Tunisia).
We have at Tring 48 specimens of this insect from halfway between Ouargla
and El Golea, March 1912 (Hartert and Hilgert) ; Bordj Mgeitla, Bordj Ferdjan
April 1909, Ghardai'a April 1911 (VV. R. and E. H.) ; Bou Saada April 1911,
Bordj Chegga March 1917 (V. Faroult) ; Amgid, north of Ideles, Oued Ag'elil,
Oued Lehin, Oued Gif-Aman, February — March 1914 (Geyr von Schweppenburg).
The British Museum has 1 $ Tunis, Staudinger and Bang- Haas.
377. Drasteria oranensis sp. nov. (PI. XVI. f. 16.)
<J $. Antennae black-brown ; head and thorax pale sandy cinnamon, central
streak on tegulae and edge of patagia deep rufous ; abdomen pale sandy
cinnamon.
Forewing sandy cinnamon, basal one-fourth almost completely saturated with
brown with a number of irregular lines and rings of black, a clear transverse convex
7
98 KOVKTATES ZOOLOGICAE XXVII. 1920.
sandy band followed by two-thirds of remainder of wing being suffused with brown
and covered with irregular black lines, leaving a whitish buff irregular patch, outer
part beyond brown greyish sandy cinnamon, with brown marginal hair line, fringe
white with brown central line and a dark cinnamon patch between veins 3 and 4.
Hindwing white on basal two-fifths, black on outer three-fifths, black central
stigma joined to black outer part in which fringe and large patch between veins
4 and apex and a small patch at vein 2 are white.
Length of forewing, 15 mm. ; expanse, 33 mm.
2 cJcJ, 3 $$ Am Sefra, May 1913 (VV. R. and E. H.).
378. Acrobyla panaceorum distincta (Rothsch.).
Armada panaceorum distincta Rothschild, Nooil. Zool. vol. xxii. p. 234. Xo. 49 (1915) (Oued Nca).
The Tring series of this insect contains 5 gg, 4 $$ from Oued Nca, Hassi
Sidi Mahmud April 1914 (Hartert and Hilgert) ; Bou Saada May 1912, Am
Sefra May 1915, Colomb Bechar March— April 1912 (V. Faroult).
379. Syneda cailino cailino (Lef.).
Heliolhis cailino Lefebre, Ann. Soc. Linn. Paris. 1827. p. 94. t. 5. f. 1 (Sicily).
Of this species we have at Tring 24 Algerian examples from Bou Saada,
Djebel Kerdada, April— May 1911-1912 (V. Faroult) ; El Kantara, March— April
1911 (W. R. and E. H., and Faroult) ; Oued Nca, April 1914 (Hartert and Hilgert).
380. Syneda cailino philippina (Aust.).
Lucanitis philippina Austaut, Le Nat. vol. ii. p. 237 (1880) (Oran).
Differs from c. cailino in its darker more rufous colouration and wider dark
outer portion of hindwings.
1 cJ, 1 $ Colomb-Bechar, March— April 1912 (V. Faroult).
381. Raphia hybris (Hiibn.).
Noct-ua hybris Hiibner, Samml. Eur. Hchmett. Xocl. f. 518 (1818).
I have received 19 specimens in all from Algeria.
6 <J<J, 9 $$ Sidi-bel-Abbes, 3 $$ Messer, September 1917 (M. Rotrou) ; 1 5
Foret de Tenira, September 1918 (P. Rotrou).
1 ^, 5?$ are normal in colouration ; the rest are very melanistic.
382. Catocala elocata (Esp.).
Koctua elocata Esper, Schmelt. vol. iv. pt. i. p. 127. No. 43. pi. xcix. ff. 1, 2 (1786).
I have received comparatively few specimens of this species.
We have 36 Mauretanian examples : Mauretania ! ! (Staudinger) ; bred
ex larvae ex Batna (Dr. A. Seitz) ; Environs de Batna, 1909-1914 (A. Nelva) ;
Bordj-ben-Aneridj October 1912, A'inDraham July — September 1912 (V. Faroult) ;
Sidi-bel-Abbes, August 1916 (M. Rotrou) ; Ain Sefra, June 19J5 (V. Faroult).
N0V1TATES ZOOLOGICAE XXVII. 1920. 99
383. Catocala oberthuri Aust.
Catocala oberthuri Austaut, Le Nat. vol. i. p. 85 (1879) (Sidi-bel-Abbes).
I have received a large series of this insect, mostly from the topotypical
locality. It appears to be much commoner in the province of Oran than in
Eastern Algeria.
The series at Tring contains 386 examples from Environs d' Alger (El Biar),
August 1905 (Captain Holl) ; Alger and Mauretania ! ! (Staudinger) ; Batna
and ex larva ex Batna, July — August 19U3-1912 (A. Nelva, Dr. A. Seitz, and
Maitre Sellier Taillefer) ; Ain Sefra, July 1915 (V. Faroult) ; Am Draham, July —
September 1911 (V. Faroult) ; Sidi-bel-Abbes, August 1918 (M. Rotrou) ; Sebdou,
September 1918 (P. Rotrou).
The series varies much in the shade of colour and accentuation of pattern in
the forewings and in the width of the black outer margin of the hindwings.
Among this series are specimens distinctly referable to ab. transient B.-H., but 1
have not received either ab. flavicans Oberth. or ab. haroldiana Oberth.
Among the Ain Sefra series are 3 <$,$ and 2 $$ of a very strange aberration,
very large and suffused with red ; this I propose to call ab. erubescens ab. nov.
The genitalia of oberthuri and elocata are alike, and there are in my series
some which look suspiciously like intermediates more or less. I am therefore
very doubtful as to the validity of the two species ; it may very well turn out that
oberthuri is a subspecies of elocata still in the making.
The British Museum has 1 $ Morocco, August — September, Meade- Waldo ;
2 (JcJ Crowley coll. ; 4 <3<S, 2 $$ Staudinger and Bang-Haas and Leech coll.
384. Mormonia dilecta powelli (Oberth.).
Catocala dilecta powelli Oberthur, Etud. Lipid. Comp. fasc. iii. expl. pi. and pi. xii. f. 13 (1909) (Daya).
The Algerian race of dilecta Hiibn. diifers from dilecta dilecta by its more
intense crimson hindwings and its greater variation in colour and pattern of
forewing. The ab. dayremi Oberth. is the extreme melanistic phase and =
ab. obscurata Spul. of dilecta dilecta Hiibn.
The large series at Tring includes most of the intergradations as well as
extreme dayremi.
We have 1,035 examples from Environs d' Alger (Captain Holl) ; Ain Draham,
September 1909-1911 (V. Faroult); Sebdou, July— August 1918 (P. Rotrou);
Sidi-bel-Abbes, August 1918 (M. Rotrou).
The British Museum has 1 J Batna, August 1910, A. E. Eaton ; 1 cj, 1 ? Ain
Draham, Staudinger and Bang-Haas.
385. Mormonia sponsa laeta (Oberth.).
Catocala sponsa laeta Oberthur, Etud. Lipid. Comp. fasc. iii. expl. pi. and pi. xii. i. 15 (1909)
(Yakouren).
The Algerian race of sponsa Linn, differs from sponsa sponsa in being larger
and brighter and more variegated with white. Mr. Oberthur has also named a
melanislic form ab. obscura.
The Algerian series at Tring is a very poor one, and mostly not in good
condition.
22 specimens from Ain Draham, September 1909-1911 (Faroult and Stau-
dinger) ; Sebdou, August 1918 (P. Rotrou) .
N0VITATE3 Zoolooicae XXVII. 1920.
386. Catocala promissa hilaris Oberth.
Oatocala promissa hilaris Oberthiir. Etud. Lipid. Cornp. fasc. iii. expl. pi. and pi. xiii. f. 17 (1909)
(Yakouren).
Catocala electra Bang-Haas. Iris, vol. xxiv. p. 41. pi. iv. f. 1 (1910) (Ain Draham).
The figure of Mr. Oberthur's hilaris from Yakouren is considerably darker
and the median black band on the hindwing is shown much broader than in any
Ain Draham specimen ; it also is smaller than most of those from there.
Dr. Jordan has examined the genital armature for me of this and European
promissa, and finds them similar. My readers will surely take me to task for
adopting Mr. Oberthur's views here as to the status of promissa and hilaris, while
I keep the much more similar insects as regards outward appearance, elocata
and oberthuri separate.
Although the genitalia are alike, I can only say that in that case they occur
together, while here hilaris replaces sponsa.
Time will show also whether after all the case may not be similar and that
oberthuri replaces elocata, but is not yet so fixed as hilaris and therefore still
produces a certain number of specimens, indistinguishable from elocata.
I have one specimen only other than Ain Draham ones ; of these latter we
possess 1'98 Ain Draham, July — August 1909-1911 (V. Faroult and Staudinger) ;
1 cS Le Tarf, July 1908 (Captain Holl).
The British Museum has 1 (J, 1 $ Ain Draham, Staudinger and Bang-Haas.
387. Catocala optata sultana B.-H.
Catocala sultana Bang-Haas, Iris, vol. xxiv. p. 42. pi. iv. f. 2 (1910) (Ain Draham).
Mr. Oberthiir is very emphatic as to the optata found in Algeria, Tunisia, and
Morocco being all one entity and found in two forms named amanda Boisd. and
selecta Boisd., and that Bang-Haas renamed this form sultana. Also because
he has received a single specimen from Tangier less strongly marked and
less bright than Bordeaux specimens, he says there is no fixity in local races,
i.e. snbspecies.
If these subspecies were absolutely fixed and showed a constant strong
difference they would be species and not subspecies. To my mind, if 75-80 per
cent, of specimens in one locality are constantly different from those of another
locality, the form is worthy of a name.
The Ain Draham form has at least 95 per cent, of the individuals larger and
the colour above brighter than optata optata, and it is also larger and brighter
than optata amanda Boisd., which only differs from optata optata in the sandy
tint and deeper rose-colour beneath. This large Mauretanian form extends all
along the Tell of Algeria, north of the Atlas, from Sidi-bel-Abbes in the west
to Ain Draham in Tunisia (Kroumerie) at least in the east.
The series at Tring contains 143 specimens from Ain Draham, July — August
1909-1911 (V. Faroult and Staudinger) ; Sidi-bel-Abbes, July— August 1917 (M.
Rotrou).
The British Museum has 1 J, 1 9 Ain Draham, Staudinger and Bang-Haas.
NOVITATES ZOOLOGICAE XXVII. 1020. 101
388. Catocala optata intermedia Hmpsn. (Bang-Haas in litt.).
Catocala optata ab. intermedia Bang-Haas iiiccl. Harnpson, Cat. Lepid. Phot. Brit. Mus. vol. xii. p. 72.
ab. 1 (1913) (Algeria (Batna)).
This is the form Mr. Oberthiir says is amanda Boisd. ; it differs from both
optata optata and optata amanda in the black central band of the hindwings being
much less irregularly dentate, and in being narrow for the costal half and suddenly
becoming broader from vein 5 where it forms a sharp angle. It also is still brighter
rose than o. amanda on the underside of the hindwings.
Our series contains 38 specimens from Batna, July — August 1910-1914
(A. Nelva and Faroult).
The British Museum has 1 $ Batna, Staudinger and Bang-Haas.
389. Catocala puerpera rosea Aust.
Catocala puerpera var. rosea Austaut, Le Nat. vol. vi. p. 391 (1884) (llorocco).
The rather poor series I have are all characteristic rosea, being larger than
puerpera puerpera Giorn. with the forewings sandy cinnamon, strongly washed
with rose.
17 examples from Am Sefra, July 1915 (V. Faroult) ; Sidi-bel-Abbes, July —
August 1917-1918 (M. Rotrou) ; Sebdou, July 1918 (P. Rotrou).
390. Catocala conjuncta vivida Warr.
Catocala conjuncta vivida Warren in Seitz, Grossschmett. Erde, vol. iii. p. 3U8. pi. 56b (1913) (Algeria).
We have 749 Algerian examples, including the type of Warren's ab. fulva
with fulvous yellow hindwings, from Sidi-bel-Abbes September 1917 (M. Rotrou) ;
Ain Draham September 1909-1911 (V. Faroult and Staudinger); Environs
d'Alger (Captain Holl) ; Sebdou, Foret de Tenira, July 1918 (P. Rotrou).
The colour of the hindwings in Mauretanian examples is deeper and richer.
391. Ephesia nymphaea (Esp.).
Noctua nympliaea Esper, Schmett. vol. iv. pt. i. p. 158. No. 52. pi. cv. f. 4 (1787) (Lyons).
This insect is also very variable as to colour and intensity of pattern of fore-
wings, many specimens almost exactly resembling Ephesia flavescens Hampson
from India, which must stand as Ephesia nymphaea flavescens Hampson.
Our Mauretanian series contains 289 specimens from Blida les Glacieres
larvae June, emerged Alger July 1908 (W. R. and E. H.) ; Tala Rana, July 1906
(Dr. Nissen) ; Mazagan, Morocco, July — September 1901-1902 (W. Riggenbach) ;
El Kantara, June 1909 (Cheli Brahim) ; Ain Draham, July 1909-1911 (V. Faroult
and Staudinger) ; Batna, July 1908-1914 (Nelva and Taillefer) ; Ain Sefra, July
1915 (V. Faroult) ; Sidi-bel-Abbes July 1917, Les Pins July 1918 (M. Rotrou) ;
Sebdou, July 1918 (P. Rotrou).
392. Catocala conversa (Esp.).
Noctua conversa Esper, Schmett. vol. iv. pt. i. pi. ev.B. ff. 1, 2, 3 (1787).
Of this species our Algerian and Tunisian examples number 228, including
the aberrations carbonaria Staud. and seminigra Warr. 156 from Tunis (Stau-
102 NOVITATES ZOOLOGICAE XXVII. 1920.
dinger) ; Ain Draham July — August 1911, Hammam R'hira June — August 1916,
north side of Djebel Zaccar August 1916, Mecheria August 1918 (V. Faroult) ;
Batna, July 1909-1912 (A. Xelva) ; Sidi-bel- Abbes July 1917, Les Pins July 1918
(M. Rotrou) ; Sebdou, July 1918 (P. Rotrou).
393. Ephesia eutychea (Treit).
Catocala evlychea Treitschke, Schmetl. Eur. vol. x. pt. ii. p. 165 (1835) (Corfu).
Although I have only the small series of 15 specimens of this southern species
from Mauretania,' it appears widely spread. It is here recorded for the first time
for our region.
4 cJcJ, 4 ?$ Hammam R'hira June 1916, 2 £<$, 1 $ Masser Mines June 1914
(V. Faroult) ; 1 J Sebdou, 1 cJ, 1 9 Foret de Tenira June 1918 (P. Rotrou) ; 1 $
Sidi-bel-Abbes, June 1918 (M. Rotrou).
[On the status of Catocala vallantini O berth. (PL XIV.)
This insect was described as a species and figured Etud. Entom. livr. xix. p. 36.
pi. vi. f. 53 (1894) (Bone) by Mr. Oberthur. In 1901 Messrs. Staudinger and
Rebel in Cat. Lepid. Pal. Faun, on p. 250 (pt. i.) place this as a species following
nymphagoga with the number 2,716 ; but make certain remarks which I translate
as follows : " Described from a single q ; judging from the type specimen, this
appears to be an aberration of the preceding species (nymphagoga), although
Staudinger would rather see in it a subspecies. In 1912, when Sir George Hamp-
son was writing vol. xii. of the British Museum Catalogue, I lent him all my large
series of Catocalas captured by Victor Faroult at Ain Draham in July — September
1911, among which were 3 vallantini and a long series of the insect Mr. Oberthur
has recorded as nymphagoga without any qualification. Among these so-called
nymphagoga are a considerable number in which the median black band of the
hindwing is in process of reduction, and there is a complete gradation from the
normal band to a band almost obsolete. Besides these there are two specimens,
one a vallantini showing a distinct shadowy trace of the band, and a second
in which the band is present, but almost gone. I suggested to Sir George
Hampson that vallantini was only an aberration of the so-called nymphagoga.
Sir George, however, after examining the series, came to a different conclusion ;
in fact he declared, and afterwards published in vol. xii. of the Catalogue, that
vallantini was a distinct species and belonged to Hubner's genus Ephesia,
while nymphagoga was a true Catocala. In 1913 in Seitz -Mr. William Warren
published vallantini as a subspecies of nymphagoga, at the same time treating some
of the Algerian examples, with a normal central band to the hindwing, as nym-
phagoga, and describing others as subspecies ! ! under the names of griseata and
albijnixta ; while others again he described as aberrations under the names of
contorta, jasciata, and julvipennis. Finally Mr. Oberthur in the volume dealt with
in this article, viz. Etudes de Lepidopterologie Comparee, fascicule xvi., treats his
so-called nymphagoga and his vallantini as two separate species ; and under
vallantini makes the following remarks : " C'est une Espece des plus tranchees
et les moins contestables parmi les Catocala a ailes iuferieures jauues de la Faune
palearctique."
When I was working at the British Museum during the months of March —
Novitates Zoolooicae XXVII. 1920. 103
July of this year (1919) preparing for this article and correcting identifications
of Mauretanian Noctuidae, I again submitted the series of Ain Draham so-called
ny7n.pha.g0ga and my 3 vallantini to Sir George Hampson, saying I could not feel
satisfied with his former decision, and was still of opinion that vallantini was an
aberration without the central band of the hindwings. He again said he was
sure they were different species, and now laid great stress on what he pointed out
as the different position and direction of the transverse lines of the forewings.
I was not satisfied with this answer, and got Dr. Jordan to examine a series
of these insects, both from Europe and Algeria.
Sir George Hampson in the Catalogue, vol. xii. gives long diagnoses of the
genera Catocala and Ephesia which I have carefully compared, and find all the
characters given by him for both genera are the same except the following :
Ephesia. "Fore and hind tibiae not spined ; mid tibiae spined. . . ."
Catocala. " Fore tibiae not spined ; mid and hind tibiae spined, the latter
only between the spurs. ..."
Dr. Jordan found both European nymphagoga and the Algerian specimens
with complete median band on hindwing, as well as vallantini, to have one or two
spines on the hind tibiae ; thus in the first place proving that vallantini is a true
Catocala and not an Ephesia. (These spines are more of the nature of stiff bristles,
protruding between the scales of the legs, and must not be confused with the
spars.)
Now, after Dr. Jordan had proved vallantini to be possessed of spines exactly
as in nymphagoga, he and I carefully compared the pattern of the forewings to test
the validity of Sir George Hampson's contention that the transverse lines on the
forewings were different in vallantini. At first sight this really appeared to be the
case, but we soon found that when the strongly dentate and sinuate postmedian
line had become obsolete, the ordinarily much less conspicuous submarginal band
stood out more plainly. This submarginal band is much further from the termen
than in most other groups of Noctuidae, and is easily mistaken for the postmedian
line in the specimens where this latter has become obliterated. There are, however,
in the series from Ain Draham a number where the postmedian line on the fore-
wings is quite as much absent as in vallantini, while the hindwings have the central
band. These at once proved to us that the Catocala vallantini Oberth. = Ephesia
vallantini of Hampson was nothing more than an extreme aberration in which
the greater part of the pattern of the forewings had become obliterated, and the
central band of the hindwings had disappeared altogether. To prove this and
also illustrate the great variability of this insect, I propose to publish a coloured
plate showing a complete gradation from the forewing with all markings extremely
sharp to the almost complete obliteration exhibited in Warren's ab. griseata $,
and also every gradation in the hindwing from one with a distinct sharply defined
central band = ab. normalis Rothsch. to the total absence of the band = ab.
vallantini Oberth.
But our thus proving that vallantini Oberth. is only an extreme aberration
does not entirely explain all points connected with this insect. When in 1901
Drs. Staudinger and Rebel made their observations on the type and unique
specimen, as it was then, of Catocala vallantini Oberth., there were no other
examples of a Catocala known from Algeria of the nymphagoga type, and this was
what chiefly induced Staudinger in opposition to Rebel to consider it to be the
Mauretanian subspecies of nympfiagoga. The large series sent from Algeria and '
104 NOVITATES ZOOLOG1CAE XXVII. 1U20.
Tunisia since 1901 make it at once apparent that Staudinger was wrong and Rebel
right as regards vallantini itself.
Now, however, the question arises, What arc the specimens with median bands
on the hindwings ? Are they true nymphagoga or are they not ? Esper described
and figured his Xoctna nymphagoga Schmett. vol. iv. pt. i. p. 159. No. 53. pis. cv.
f. 5 and cv.6. f. 5 (1787) from Lyons and South Italy, and I have examined at
Tring a series of 140 European specimens consisting of 8 without any locality and
138 from Quillery, France ; Landes, S. France ; Germany ; Dalmatia ; Austria ;
HerculesfiirdS, Hungary; Sorgento, Sardinia; Sicily ; and Amanus Mts.,
Syria, and I have compared them with 367 Algerian and Tunisian examples.
Among the European examples are specimens of the ab. anthracita Th. Mieg.,
ab. tinolia Led., ab. curvifascia and ab. nubilosa Schulze, as well as the type of ab.
albinata Warr. ; while among the Mauretanian examples are the ab. vallantini
Oberth., ab. normalis Rothsch., ab. leucomelas Oberth., ab. albimixta Warr., ab.
griseata Warr., ab. jasciata Warr., ab. fulvipennis Warr., and ab. contorta Warr.
I find the general run of Mauretanian examples (in fact 95 per cent.) are smaller,
and in all of them the yellow of the hindwing is very bright, and there is much
more tendency for the pattern of the forewings to become obliterated, while the
central band of the hindwings shows all degrees of reduction till it is absent
altogether in typical ab. vallantini.
In the whole of the 146 European nymphagoga at Tring there is no specimen
exhibiting any reduction of this central band, nor is there in the British Museum
series. From all these points of difference, it is clear that the Mauretanian
nymphagoga differ from the European ones. It remains to be seen what the}' ought
to be called. Of the 8 names applied to Mauretanian specimens, that of vallantini
Oberth. is not only the oldest but also was not used in an aberrational sense when
first given. Therefore the name for the Mauretanian subspecies of nymphagoga
must stand asC'atocala nymphagoga vallantini Oberth., with two extreme forms ab.
normalis Rothsch. with complete median band to the hindwing and ab. vallantini
Oberth. with this band absent.]
394. Catocala nymphagoga vallantini Oberth. (PI. XIV. ff. 1-24 & 30-39.)
Catocala vallanlini Oberthiir, Etud. Entom. livr. xix. p. 36. pi. vi. f. 53 (1894) (Bone).
This subspecies differs from nymphagoga nymphagoga Esp. in its generally
smaller size, brighter colouration, especially the yellow colour, and the narrower
outer margin of the hindwing, and in the strong tendency to obliteration of pattern
of forewing and the central band of the hindwing. There are two extreme forms :
one ab. normalis ab. nov. with pattern of forewing and central band of hindwing
strongly defined, and ab. vallantini Oberth. with the pattern of forewing almost
obliterated and the band of hindwing absent. Between these extremes all inter-
gradations occur ; for the names of the various intermediates see antea.
The Tring series contains 376 Mauretanian examples from Ain Draham,
Tunisia, July 1909-1911 (V. Faroult and Staudinger) ; Ax larva, the larvae Blida
les Glacieres May, emerged Alger July 1908 j(W. R. and E. H.) ; Tala Rana,
Kabylie July 1908, Mezarir July 1906, Leila Kredidja, Kabylie July 1907
(Dr. Nissen) ; Sebdou, Foret de Tenira, July 1918 (P. Rotrou) ; Sidi-bel-Abbes,
July 1918 (M. Rotrou) ; El Mahouna, July 1919 (V. Faroult).
Novitates Zoolooicae XXVII. 1920. 105
[Note on the genus Ephesia Hiibn.
Sir George Hampson takes as the type of Ephesia, Phalaena fulminea Scop.
On examination of the long series of the species at Tring, Dr. Jordan found
spines present on the hind tibiae in some individuals, while they were absent in
others.]
395. Anua tirhaca (Cram.).
Phalaena tirhaca Cramer, Pap. Exot. vol. ii. pt. xv. p. 110. pi. elxxii. f. E. (1777) (Cape of Good
Hope).
Of this conspicuous insect the Mauretanian series at Tring comprises 36
examples from El Kantara, March 1911 (W. R. and E. H.) ; Batna September
1910, Ai'n Draham September 1911, Guelt-es-Stel September — October 1912-
1913, Bou Saada July 1911, Bordj -ben- Aneridj October 1912, Perregaux October
1915, Lalla Marnia 1914 (V. Earoult) ; Sidi-bel- Abbes, September 1917 (M. Rotrou) ;
Environs de Taourirt, July 1918 (M. Rotrou) ; Hammam R'hira, June 1918 (V.
Faroult).
[Minucia lunaris (Schiff. & Den.).
Pftatoena Smarts Schiffermiiller arid Denis, Ank. Syst. Werk: Schmett. Wienergeg. p. 94 (1775) (Vienna).
Mr. Oberthur records the Mauretanian race of this species under the name
of the European form, and only treats certain striking aberrations as such under
the names of maura, rufa, and murina. It is quite true that while Mr. Oberthur
has several hundred specimens from Mauretania, the Tring Museum has only 89,
but yet among those 89 there are none like typical European specimens. I
therefore propose to separate the Mauretanian race as a separate subspecies, and as
it is very appropriate I shall adopt for it Mr. Oberthur's name of maura, although
only given to an aberration.]
396. Minucia lunaris maura (Oberth.).
Pseudophia lunaris ab. maura Oberthur, Etud. Enlom. livT. ix. p. 39. pi. iii. f. 13 (1884) (Sebdou).
The Tring series of I. maura contains 5 ab. rufa Oberth., 4 ab. murina Oberth.,
but no typical maura, all the rest being intermediates between murina and maura.
89 examples from Batna, Lambessa (A. Nelva) ; Khenchela May 1912, Souk
Ahras April 1914 (W. R. and K. J.) ; Sebdou, Foret de Tenira, April 1918 (P.
Rotrou) ; Lambessa May 1909, Environs d' Alger May 1908 (W. R. and E. H.).
So far as I have seen, the sandy cinnamon-grey colour of the European form
is never found in Mauretanian specimens, so that the diagnosis should read :
" Differs from I. lunaris in the less sandy, more silvery grey ground-colour and
in the much greater frequency of aberrations with red, olive, or mouse-grey ground-
colour, and with obliterated bands."
[The genus Clytie and the forms allied to illunaris Hiibn.
Mr. Oberthur records Clytie illunaris from Algeria and says he has received
specimens from various places all extremely variable, some being identical with
illunaris, while others agreed with sancta Stdgr. and syriaca Bugn. I myself have,
in addition to describing Clytie arenosa as new, from time to time recorded various
106 NOVITATES ZOOLOGICAE XXVII. 1920.
Clyties from Mauretania, viz. terrulenta Christ. ; ddunaris Stdgr. ; and syndaja
Hmpsn.
Now, the various species and races of this genus are very puzzling, owing
mainly to the variation in the submarginal or postdiscal band on the forewings.
Sir George Hampson enumerates the following as distinct species : devia Swinh. ;
scotorrhiza Hmpsn. ; sancta Stdgr. ; illunaiis Hiibn. ; haifae Habich ; distincta
B.-H. ; sydaja Hmpsn. ; aretwsa Rothsch. ; syriaca Bugn. ; sublunaris Stdgr. ;
nabataea Hmpsn. ; ddunaris Stdgr. ; and terrulenta Christ. Mr. Warren in Seiiz
has described and figured in addition to these luteonigra from the Amu Darya. I
have non-Algerian examples of all these, except distincta B.-H., scotorrhiza Hmpsn.,
devia Swinh., and nabataea Hmpsn., more or less from their typical localities, and I
find that I have among my Algerian material certainly the following : nabataea
Hmpsn., arenosa Rothsch., sancta Stdgr., and syriaca Bugn., but I have not got a
single specimen at all agreeing with illunaris. In addition to these 4 I have 1 ?
from Am Draham which agrees exactly with Warren's luteonigra, except that it is
larger than the 3 Amu Darya examples. There remain the insects I recorded
as sublunaris and terrulenta.
The series collected by Herr Geyr von Schweppenburg in and north of the
Hoggar Mountains recorded by me as ddunaris are, I am now convinced, only
very fresh and sharply marked sancta Stdgr. The insects recorded as terrulenta
are certainly very small, but I am more inclined now to admit an error of identi-
fication and consider them sandy sancta.]
397. Clytie sancta (Stdgr.).
Pseudophia sancta Staudinger, Iris, vol. x. p. 301 (1S97) (Palestine).
By far the larger number of Clytie at Tring consist of this form.
95 examples from South Oued Mya, May 1912 (Hartert and Hilgert) ; Oued
Ahmra, Oued Ag'elil, Oued Gif-Aman, Oued Tamoudat, Ideles, north of Ideles,
March 1914 (Geyr von Schweppenburg) ; Am Sefra July 1915. Masser Mines,
June 1914,Guelt-es-Stel October 1912, El Mesrane June 1913,Bou Saada May 1911,
El Kantara March— August 1911-1917, Batna 1910 (V. Faroult) ; Les Pins
August 1918 (M. Rotrou).
398. Clytie arenosa Rothsch.
Clytie arenosa Rothschild, Novit. Zool. vol. xx. p. 123. No. 69 (1913) (South Oued Mya).
Of this rare species we have at Tring 3 specimens : 1 <J, 1 $ Oued Mya, May 1912
(Hartert and Hilgert) ; 1 $ Oued Tahihout, April 1914 (Geyr von Schweppenburg).
399. Clytie syrdaja Hmpsn.
Clytie syrdaja Hampson (Pseudophia syrdaja, B.-H. ined.). Cut. Lepid. Phal. Brit. Mils. vol. xiii,
p. 293. No. S102. pi. ccxxxi. ft". 19, 20 (1913) (Aulie Ata).
1 $ El Mesrane June, Guelt-es-Stel July 1913 (V. Faroult).
400. Clytie luteonigra Warr.
Clytie luteonigra Warren in Seitz, Grossschmett. Erde, vol. 3. p. 338. pi. fi2rf. (1913) (Amu Darya).
1 ? Ain Draham, Tunisia, September 1911 (V. Faroult).
Novitates Zoolocicae XXVII. 1920. 107
401. Parallelia algira (Linn.).
Phalaena algira Linnaeus, St/st. Nat. edit. xii. p. 836. No. 98 (1707) (Algeria).
There appear to be two forms of this species : one, a smaller one with the
median band narrow and much constricted in the centre on forewing and more
or less obscured by dark scales giving it a mauve tinge and with the band on
hindwing very narrow ; and two, a larger one with the band on forewing broad
and very little constricted and white and the band on hindwing much broader.
This latter has been placed together with Syrian, Egyptian, and Arabian
specimens under albivitta Guen. by Warren, who says in Seitz : " Always larger than
algira," forgetting that Guenee says his albivitta is the same size as algira. Warren
also attributes the name albivitta erroneously to Moore instead of Guenee.
Sir George Hampson unites torrida Guen., albivitta Guen., jestina Walk.,
olympia Swinh., and algiroides Schultz under algira, and gives it an enormous
range from France to Turkestan, all over Africa, Asia Minor, India, and Ceylon.
I have too small a material to judge if he is right or whether there are two or more
species or a series of subspecies.
We have at Tring 59 Mauretanian examples from Environs d'Alger (Dr.
Nissen); Hammam Meskoutine, May 1909-1914 (W.R.,E. H., and K. J.); Hammam
R'hira, May— August 1908-1916 (W. R. and K. J., and Faroult) ; Ai'n Draham,
Tunisia August 1911, north side of Djebel Zaccar August 1916, Guelt-es-Stel
September 1913, Ai'n Sefra July 1915, Perregaux October 1915, Aflou October
1916 (V. Faroult) ; Oran, April 1913 (W. R. and E. H.) ; Ljebel Kerdada May 1912,
El Kantara August 1917 (V. Faroult) ; Biskra, June 1912 (Hartert and ililgert) ;
Sebdou, Foretde Tenira, June 1918 (P. Rotrou) ; Sidi-bel-Abbes, September 1917
(M. Rotrou) ; El Mahouna, July 1919 (V. Faroult).
402. Grammodes stolida (Fabr.).
Nocliia ptolida Fabricius, Syst. Entom. p. 599. No. 3S (1775) (East India).
Of this species the series from Algeria at Tring comprises 44 specimens from
Ghardai'a May, Oued Nca June 1912 (Hartert and Hilgert) ; Guelt-es-Stel July —
September 1912-1913, Tilghemt April 1912, Bou Saada April 1912, El Outaya
August 1918, Batna July 1910, north side of Djebel Zaccar August 1916, Alger
January 1914 (V. Faroult) ; El Kantara, June — August 1909-1917 (Cheli Brahim
and Faroult); Sidi Ferruch, July 1911 (A. Thery) ; Sidi-bel-Abbes, Les Pins,
May— September 1917-1918 (M. Rotrou) ; Sebdou, Foret de Tenira, August 1918,
(P. Rotrou).
The British Museum has 1 $ Batna, August 1910, A. E. Eaton.
403. Grammodes boisdefirei (Oberth.).
Ophiusa hoisdeffrei Oberthiir, Etiul. Entom. livr. i. p. 54. pi. 4. f. 6 (1876) (Biskra),
2 c?c?, 1 9 Biskra, March 1914 (W. R. and E. H., and Staudinger).
The British Museum has 1 $ Batna, August 1910, A. E. Eaton; 3 £$, 2 ?$
Hammam-es-Salahin, April 1904, Lord Walsingham.
404. Grammodes geometrica (Fabr.).
Noctva geometrica Fabricius, Syst. Entom. p. 599. No. 37 (1775) (East India).
1 ? Aiin Draham, Tunisia, August 1911 ; 1 q Hammam R'hira, May 1917 (V.
Faroult).
108 NOVITATES ZOOLOGICAE XXVII. 1920.
[On Cerccala scajmlosa Hiibn., sana Stdgr., insana Herr-Sch.,
and algiriae Oberth.
Mr. Obertbiir is continually complaining that other authors neglect his
work and do not trouble to look up his species ; in the case of the Mauretanian
Cerocalas it is he who has neglected other people's work, and persisted in uniting
sana and his own algiriae specifically with scapulosa, with which they have nothing
to do — being very distinct species differing from each other and from scapulosa
in the genital armature, in the antennae, and in the legs. Sir George Hampson
in vol. xiii. of the Catalogue already separated the 3 forms into 3 species, but after
catching a large series at Am Sefra and receiving many from elsewhere I was not
sure if there might not be more and I asked Dr. Jordan to investigate the material
we possessed. This he did very thoroughly, and published the result in
Novitates Zoologicae, vol. xxii. pp. 267-270, text figures 1-10 (1915). While
Sir George Hampson is right in separating this group of Cerocala into 3 species,
he has not got the synonymy of the two Mauretanian species quite right, as
scapulosa Luc. nee Hiibn. belongs to sana and not to what he calls insana, but
which must stand as algiriae Oberth. I consider the figure of Herrich-Schaffer
and his locality so doubtful that the name cannot be used for either of the Maure-
tanian species and I call them Cerocala sana Stdgr. and Cerocala algiriae Oberth.
Mr. Oberthiir says he has never received what he calls the typical form of scapu-
losa, as found in Andalusia, from Algeria ; this is quite natural, for the true scapu-
losa is a perfectly distinct species from the two found in Mauretania and so far
has never been recorded from south of the mediterranean, although the 2 other
species have been at various times called scapulosa and otherwise confused with it.
Mr. Oberthiir, at the end of his article on Cerocala scapulosa, somewhat qualifies
his statements by saying that the fact of not finding the larger and darker true
scapulosa in Mauretania might lead one to consider algiriae a distinct species.
As a matter of fact Sir George Hampson's, William Warren's, and lastly Dr. Jordan's
exhaustive studies and dissections of these Cerocalas have proved beyond doubt
that there are 3 distinct species of Cerocala of this section, distinct in structure
of genitalia, legs, and antennae as well as in appearance, viz. Cerocala scapulosa
(Hiibn.), Cerocala algiriae Oberth., and Cerocala sana Stdgr.]
405. Cerocala algiriae Oberth.
Cerocala scapulosa var. algiriae Oberthiir, Etud. Entom. vol. i. p. 55. pi. iv. f. 7 (1S70) (Bou Saada).
Cerocola insana Hampson, Cat. Lipid. Phal. Brit. Mus. vol. xiii. p. 270. No. 8070 (1913) (Biskra).
? ? Grammodes insana Herrich-Schaffer, Aussereur. Schrnett. i. 395 (1850) (Cape of Good Hope).
Cerocala scapulosa form, biskrensis Culot, Noct. el Geom. d'Eur. pt. i. vol. ii. p. 182. pi. 73. i. 5 (1910)
(Biskra).
The series of this species at Tring includes individuals agreeing both with
the figures of algiriae Oberth. and biskrensis Culot, the latter being rubbed speci-
mens, and consists of 194 examples from Colomb Bechar March and April 1912,
Bou Saada March— May 1911-1912, Tilghemt April 1912, Laghouat March 1912,
El Hamel May 1912, Bordj Chegga and Bir Stil March 1917 (V. Faroult) ; Ghardaia
and Tilghemt, April 1911 (W. R. and E. H.) ; Guelt-es-Stel, March— April 1912-
1913 (W. R. and K. J., and Faroult); El Kantara March— April 1911, Aflou
October 1916 (V. Faroult); halfway between Ouargla and El Golea, Hassi el
Hadjar, Arefidji north of Ouargla, Bordj Chegga, north of El Golea, February —
NOVITATES ZOOLOOICAE XXVII. 1920. 109
March 1912, Hassi Sidi Mahmoud and Oued Nca April 191-1 (Hartert and Hilgert) ;
Biskra, March 1908 (W. R., and E. H.) ; Gafsa, Tunisia (Staudinger) ; Ain Sefra,
May 1913-1915 (W. R. and E. H., and Faroult).
The British Museum has 1 <$ Biskra, April 1894, A. E. Eaton ; 1 cJ Biskra
March 1906, 2 <$<$, 2 $$ Hammam-es-Salahin March — April 1904, Lord Walsing-
ham ; 1 $ Tozeur, Tunisia, 1913, G. C. Champion.
406. Cerocala sana Stdgr.
Cerocala scapulosa var. sana Staudinger, Cat. Lepid. Pal. Faun. p. 241. No. 2594a (1901) (Antioch,
Syria).
Cerocala scapulosa var. Lucas, Ann. Soc. Entom. France (2) 8. p. 103. pi. 2. f. 3 (1850) (Djebel Amour).
Cerocala scapulosa var.insana Staudinger, Cat. Lepid. Europ. Faun. edit. ii. p. 135. No. 1923a (1871)
(Syria).
Of this species the series at Tring consists of 192 examples from Ain Sefra,
May 1912-1915 (W. R. and E. H., and Faroult) ; Biskra March 1908, Kef-el-Dor,
Bordj Ferdjan and Bordj Mgeitha April 1909 (W. R. and E. H.) ; South Oran
(Staudinger) ; Colomb-Bechar March— April 1912, Bou Saada May 1911-1912,
Laghouat March 1912 (V. Faroult) ; Bordj Chegga, Nca ben Rzig, halfway
between Ouargla and El Golea, Arefidji north of Ouargla, north of El Golea,
Hassi el Hadjar February — March 1912 (Hartert and Hilgert) ; Ghardaia, April
1911 (W. R. and E. H.) ; El Hamel May 1912, Guelt-es-Stel May 1913, Djelfa
May 1913 (V. Faroult) ; Oued Nca April 1914 (Hartert and Hilgert) ; Hammam
R'hira, May 1916 (V. Faroult).
407. Antarchaea viridaria (Clerck).
Phalaena viridaria Clerck, Icones Ins. Rar. sect. i. pi. 9. f. 12 (1759).
This species is not recorded by Mr. Oberthur ; all my 6 specimens belong
to the ab. modesta Car. with the maroon colour almost absent.
5 Hammam R'hira, May 1911 (W. R. and E. H.) ; 1 Souk Ahras, April
1914 (W. R. and K. J.).
408. Antarchaea sanctiflorentis aurantiaeus subsp. nov.
cJ$. Differ from sanctiflorentis sanctiflorentis Boisd. from Spain by theorange-
rufous.ground-colour and the generally larger size, outer half more or less suffused
with maroon red.
Mr. Oberthur records sanctiflorentis from Ain Draham with no remarks.
If he really got typical grey sanctiflorentis from Ain Draham, my insect is a new
species ; but until I have seen Mauretanian specimens of true sanctiflorentis I prefer
to treat this form as a good subspecies only.
9 Ain Draham, Tunisia, July 1911 (V. Faroult).
409. Antarchaea erubescens (B.-H). (PL XVI. f. lo.)
Prothymnia erubescens Bang-Haas, Iris, vol. 24. p. 40. pi. iii. f. 11 (1910) (South Oran).
The figure given in Seitz appears to be quite wrong. My $ is the second
specimen recorded and differs from the $ in the whole forewings being so strongly
110 NOVITATES ZOOLOGICAE XXVII. 1920.
suffused with red that the yellow ground so apparent in the $ is entirely invisible ;
the median line of forewings more complete and visible than in the (J.
1 $ Djebel Mekter, nr. Ai'n Sefra, 1,600-1,900 metres = 5,200-6,175 ft., May
1913 (W. R. and E. H.). •
410. Rivula sericealis distincta subsp. nov.
$. Differs from sericealis sericealis Schiff. and Den. in having the curved band,
leading from the reniform obliquely to the inner margin, distinctly defined instead
of being a shadowy outline only ; smaller and less yellow, more cream-buff.
$. With similarly well-defined band, but not so extended as in <J, and
ground-colour yellower.
1 (J Oued Hamidou, June 1912 (V. Faroult) ; 1 J Hammam Meskoutine, May
1909 (W. R. and E.H.) ; 1 $ Environs d'Alger, May 1908 (W. R. and K. J.) ;
1 <J Sidi-bel-Abbes, October 1917 (M. Rotrou) ; 1 (J Sebdou, September 1918 (P.
Rotrou).
411. Parascotia nisseni Turati.
Parascotia nisseni Turati, 11 Natur. Sicil. vol. xx. p. 34 (1908) (Alger).
Of this rare species I have only received 5 specimens. Neither Mr. Culot
nor Mr. Oberthur mention the insect.
1 Environs d'Alger, May 1906 (Dr. Nissen) (co-type) ; 1 Ain Draham, Tunisia,
July 1911 (V. Faroult) ; 1 Hammam Meskoutine, May 1914 (VV. R. and K. J.) ;
1 Hammam R'hira, May 1916 (V. Faroult) ; El Mahouna, June 1919 (V. Faroult).
412. Zethes insularis Ramb.
Ztthe-s insularis Rainbur, Ann. Soc. Entorn. France, vol. ii. p. 29. pi. 2. f. 1 (1833) (Ajaccio).
Of this Mediterranean species the Mauretanian series at Tring contains 38
examples from Hammam R'hira, May — September 1908-1917 (W. R., E. H., and
K. J., and Faroult) ; Hammam Meskoutine, May 1914 (VV. R., E. H., and K. J.) ;
north side of Djebel Zaccar August 1916, Guelt-es-Stel May 1913, Oued Hamidou
June 1912, Ain Sefra July 1915 (V. Faroult) ; El Mahouna, June 1919 (V. Faroult).
One of the 3 Am Sefra specimens stands out from the rest of the 37 examples
by its brilliant colouration and very sharply defined markings.
413. Hydrilla caliginosa (Hiibn.).
Noctua caliginosa Hiibner, Samml. Eur. Schmelt. Noel. No. 474 (1818).
I have only received a single example of this species from Mauretania.
1 <J Blida, December 1915 (V. Faroult).
414. Miselia softa luteocinnamomea subsp. nov. (PI. XVII. f. 7.)
Differs from sojla softa Stdgr. from Palestine in its sandy rufous-cinnamon
not grey ground-colour and in the pattern being more sharply defined.
1 (J El Kantara March— April 1911, 1 <J Perregaux October 1915, 2 Jd Bou
Saada May 1911 (V. Faroult).
There are 1 J, 1 $ in the British Museum from Hammam-es-Salahin, May
1904 (Lord Walsingham).
NOV1TATES ZOOLOGICAE XXVII. 1920. Ill
415. Miselia peregrina (Treit.).
Hadena peregrina Treitschke, Schmett. Eur. vol. v. pt. i. p. 330. No. 11 (1825) (South of France).
I have received 2 specimens of this species.
1 tj, 1 $ Tebessa (M. Bartel).
416. Bryophila maeonis Led.
Bryophila maeonis Lederer, Ann. Soc. Enlom. Belg. vol. ix. pp. 63 and 78. pi. iii. f. 8 (1865)
(Kisilgye-Aole).
1 (J Environs de Batna (A. Nelva).
417. Athetis euxoides sp. nov. (PI. XVI. f. 8.)
$. This is a giant among the Athetis and is like nothing hitherto described.
Antennae brown ; head and thorax purple-brown ; abdomen wood grey.
Forewings basal two-thirds purplish maroon-brown irrorated and streaked
with grey, outer one-third brighter maroon strigillated with grey ; a marginal
maroon-black band, fringe greyish rufous. Hindwings basal two-thirds semi-
hyaline white washed with grey, outer one-third more strongly suffused and
saturated with grey.
Length of forewing, 18 mm. ; expanse, 42 mm.
1 $ Batna (Nelva coll.).
418. Athetis persimilis sp. nov. (PI. XVI. f. 9.)
J. Similar to the dark form of quadripunctata F., but without the rufous
submarginal band and with shorter broader wings. Head and thorax dark
brownish grey ; abdomen slightly paler.
Forewings dark brownish grey, costal edge deep buff, the black caradrine
spots very conspicuous ; an oblique dark band from first spot, post-discal area
sooty black-brown with huffish lines. Hindwings white, veins and edge of wing
brownish grey.
Length of forewing, 15 mm. ; expanse, 35 mm.
3 S3 Souk Ahras, Apfil 1914 (W. R. and K. J.) ; 1 J Sidi-bel-Abbes,
September 1917 (M. Rotrou).
[Agrotis picata B.-H.
Agrotis picata Bang-Haas Iris, vol. xxvi. p. 140 (1912) (Batna).
This species is near glareosa Esp. and is most striking owing to the very
dark hindwings.
I have not received this and Mr. Oberthtir does not record it.]
[Epia cinochrea (Chret.).
Dianthecia cinochrea Chretien, Ann. Soc. Enlom. France, vol. lxxix. p. 500 (1911) (Gafsa).
This species is nearest to silenes Hiibn., but smaller and paler purer grey.
I have not received it, and Mr. Oberthiir believes it to be Pronolestra
silenides Stdgr.]
112 NOVTTATES ZOOLOOICAE XXVII. 1920.
[Miselia grisea (D. Lucas).
Polia grisea Daniel Lucas, Bull. Soc. Entom. France, 1908, p. 93 (Kebili, S. Tunisia).
I have not received this species.]
[Crosia hachem Dupont.
Crosia hachem Dupont, Bull. Soc. Entom. France, 1910, p. 369, text fig. 1 (Mascara).
I have not received this, and the type remains unique. Mr. Oberthiir should
have acknowledged this as it is figured.]
[Parastichtis spinosa (Chret.).
Hadena spinosa Chretien, Ann. Soc. Entom. France, vol. Ixxix. p. 501 (1911) (Gatsa).
This fits better into Parastichtis than Eumichtis and is surely one of the
Zenobiinae. I have never received it.]
[Athetis distigma (Chret.).
Caradrina distigma Chretien, Bull. Soc. Entom. France. 1913, p. 282 (Biskra).
The author places this near atriluna Guen. ; but I think it comes next to my
oberthuri and proximans. I have not received it.]
[Athetis halimi (Chret.).
Caradrina halimi Chretien, Bull. Soc. Entom. France, 1913, p. 282 (Biskra).
I have not received this species.]
[Proxenus bicolor Chret.
Proxenus bicolor Chretien. Bull. Soc. Entom. France, 1913, p. 304 (Biskra).
I have not received this species.]
[Bombycia angularis (Chret.).
Calophasia angularis Chretien, Arm. Soc. Entom. France, vol. Ixxix. p. 504 (1910) (Gafsa).
I have no Tunisian Bombycia of this group, and as I said antea under Bombycia
chretieni mihi I am not sure whether the Sakamodi example enumerated under
that species is not angularis.
This question must await more material.]
419. Eublemma nelvai sp. nov. (PI. XVI. f. 24.)
(J. Antennae amber ; head and tegulae pale cinnamon, rest of thorax
apparently also pale cinnamon ; abdomen dark cinnamon-grey.
Fore wings pale rosy lavender, costal edge buff passing into rufous towards
apex, a cinnamon rufous median line edged with cream- buff strongly angled
outwards at discocellulars, inside this angle is the sooty black reniform, a
postmedian rather less distinct line rufous also angled outwards, a submarginal
broken line of sooty black spots, marginal fine cream-colour edged inwardly
with rufous, fringe rufous. Hindwings mouse-grey, marginal line cream edged
inwardly with rufous ; fringe grey, tinged with rufous.
Length of forewing, 9 mm. ; expanse, 20 mm.
1 (J Environs de Batna, 1914 (A. Nelva).
NOVITATES ZOOLOQICAE XXVII. 1920. 113
Mr. Oberthiir, following Guenee 's classification, omits from his list all the
insects placed by Guenee in his Deltoid.es. This group, according to Guenee,
contains what have hitherto been called the Hypeninae, together with several
of the Noctuinae such as Bivula.
The insects formerly called Hypeninae now make up the fourteenth sub-
family of Noctuidae and must stand as Polypogoninae, according to Sir George
Hampson's classification.
420. Nodaria cornicalis (Fabr).
Phalaena cornicalis Fabricius, Entom. Syst. vol. iii. pt. ii. p. 229. No. 374 (1794) (India).
Herminia nodosalis Herrich-Schafier, Syst. Bearb. Schmett. Eur. vol. ii. p. 385. No. 607. pi. 118. f. 6U5
(1845) (Sicily).
Nodaria externalis Guenee, Hist. Nat. Ins. Spec. Gin. Lipid, vol. viii. p. 64. No. 78 (1854) (Coast of
Coromandel).
I consider both these insects to be the same, although the late Mr. William
Warren in Seitz, Grossschmetterlinge der Erde, kept them separate. Fabricius's
name is undoubtedly the oldest.
We have at Tring 35 Mauretanian examples from Environs d'Alger, May —
November 1905-1908 (W. R. and E. H., Dr. Nissen and Captain Holl) ; Oued
Hamidou June 1912, Bordj-ben-Aneridj October 1912, Ain Draham September
1911, Bou Saada June 1912, Perregaux October 1915, Moroccan Frontier May
1914 (V. Faroult) ; Rabat, Morocco, January 1913 (A. Thery) ; Blida, November
1915 (V. Faroult) ; Sebdou, September 1918 (P. Rotrou).
421. Hypena obsitalis (Hiibn.).
Pyralis obsitalis Hiibner, Samml. Eur. Schmett. Pyr. ff. 164, 165, 179 (1827).
Of this insect the Mauretanian series at Tring consists of 119 specimens from
Mazagan, Morocco, Mhoila nr. M.-zagan, January — April 1902-1903 (W. Riggen-
bach); Rabat, Morocco, January 1913 (A. Thery); Environs dAlger, March —
May 1908-1912 (W. R., E. H., and K. J., and Dr. Nissen); Hammam R'hira
May 1916, north side of Djebel Zaccar August 1916, Ain Sefra July 1915, Blida
November 1915 (V. Faroult) ; Sidi-bel-Abbes, August — September 1917 (M.
Rotrou) ; Sebdou, Foret de Tenira, May — August 1918 (P. Rotrou).
422. Pechipago (Zanclognatha auet. ) crinalis (Treit.).
Herminia crinalis Treitschke, Schmett. Eur. vol. vii. p. 17. No. 8 (1S29).
We have of this species 57 Mauretanian examples from Environs dAlger,
May 1906 (Dr. Nissen) ; Hammam R'hira, May— June 1913-1916 (W. R. and
E. H., and Faroult) ; north side of Djebel Zaccar August 1916, Ain Draham
September 1916, Bou Saada October 1911, Blida November 1915 (V. Faroult);
Sidi-bel-Abbes, August — September 1917 (M. Rotrou) ; Sebdou, Foret de Tenira,
September 1918 (P. Rotrou).
8
114 Novitates Zoolooicae XXVII. 1920.
423. Pechipago flavicrinalis sp. nov.
<J. Differs at a glance from criiialis Treit. in the lunate reniform and much
postmedian line of forewing, and in the greyish sandy-yellow colour of wings and
body.
9. Similar, but even brighter sand y- yellow colour.
Length of forewing, <J 13-16 mm., $ 12-15 mm. ; expanse, (J 29-35 mm.,
$ 27-33 mm.
5 £<$, 8 $$ from Am Draham August — September 1911, Bou Saada
October 1911 (V. Faroult) ; Hammam R'hira, May 1913 (W. R. and E. H.) ;
Environs d'Alger, May 1908 (W. R. and K. J.); Ain Draham (Staudinger) ;
Philippeville, bred from egg (Andreas); Foret de Yakouren, May 1909 (Mrs.
Walsh).
424. Ophiuche lividalis (Hubn.).
Hypena lividalis Hiibner, Beitr. Gesch. Schmett. vol. ii. p. 4. No. 1 (1791).
Of this species I have 2 specimens from 1 <J Sidi-bel- Abbes, September 1917
(M. Rotrou) ; 1 <J Environs de Tunis, 1916 (M. Blanc).
The Sidi-bel- Abbes $ expands 22 mm., while the Tunis one expands 32 mm.
There are doubtless several other species of Polypogonime in Mauretania,
but I cannot find records of any others.
In order to complete the list of the recorded Noctuidae from Mauretania,
I enumerate here certain Westermaniinae and others already enumerated by me
in the earlier portions of these supplemental notes.
425. Nycteola falsalis (Herr.-Sch.).
iV ijcteola falsalis Herrich-Schaffer, Deulscli. Ins. vol. i. pi. 106. f. 1 (1829) (Germany).
Our series at Tring from Mauretania consists of 58 examples from Environs
d'Alger, May 1908 (W. R. and K. J.); Sidi Ferruch, July— August 1911 (A.
Thery) ; Hammam Meskoutine, April— May 1914 (W. R., E. H., and K. J.) ;
Hammam R'hira May 1911-1913 (W. R. and E. H.) ; Guelt-es-Stel, April 1912
(W. R. and K. J.) ; Sidi-bel-Abbes, September 1917 (M. Rotrou) ; Sebdou, May
1918 (P. Rotrou).
The British Museum has 1 Hammam -es-Salahin, March 1904, Lord Walsingham.
One of the Sidi-bel-Abbes examples has the median band absent all but a
round black spot above inner margin.
426. Sarrothripus revayana (Scop.).
Tortrix revayana Scopoli, Annus Nat. Hist. vol. v. p. 110 (1772) (Germany).
Our Mauretanian series contains 17 specimens from Environs de Batna, 1911—
1912 (A. Nelva) ; Sidi-bel-Abbes, July— September 1917 (M. Rotrou) ; Sebdou,
June 1918 (P. Rotrou) ; Masser Mines June 1914, Ain Sefra July 1915, Ain Draham
July— September 1911 (V. Faroult); Hammam Meskoutine, May 1909 (W. R.
and E. H.).
10 of these are ab. glaucana Lampa ; 4 are ab. obscura Warr. ; 1 is ab.
lisculana Schmid ; and 2 are ab. ilicana Fabr.
Novitates Zoolooicae XXVII. 1920. 115
427. Earias chlorophyllana Stdgr.
Earias chlorophyllana Staudinger, Iris, vol. iv. p. 249 (1891) (Mardin).
When writing on this species {Novit. Zool. vol. xxiv. p. 404 (1917)) I had no
Mauretanian specimens, but since then the Tring Museum has received 6 speci-
mens from Sidi-bel-Abbes, August — September 1917 (M. Rotrou).
428. Earias albovenosana Oberth.
Earias albovenosana Oberthiir, Etud. Lipid. Comp. fasc. xiii. p. 27. pi. cdxxxvi. ff. 3767, 3768 (1917)
(Lambessa).
The Tring series of this now numbers 10 examples from Aiin Draham
September 1911, Khenchela June 1911, Hammam R'hira June 1917, Ain Sefra,
June 1915 (V. Faroult) ; Sidi-bel-Abbes, June— August 1917 (M. Rotrou) ; Foret
de Tenira, September 1918 (P. Rotrou).
429. Earias chlorion Ramb.
Earias chlorion Rarabur, Cat. Syst. Lipid. Andal. livr. ii. pi. xv. f. 6 (1868) (Andalusia).
Of this species there are 2 at Tring from Biskra, 1911 (W. R. and E. H.).
430. Earias insulana (Boisd.).
Torlrix insulana Baisduval, Faun. Madag. p. 121. pi. 16. f. 9 (1833) (Madagascar).
Of this species we have 2 Mauretanian specimens from Sidi-bel-Abbes,
September — October 1917 (M. Rotrou).
431. Hylophila africana Warr.
Hylophila africana Warren in Seitz, Grossschmett. Erde, vol. iii. p. 298. pi. 53m. (1913) (Ain
Drabam).
1 <J, 1 ? Ain Draham, <£ July 1911, $ no date (V. Faroult and Max Bartel).
432. Abrostola tripartita (Hum.).
Phalaena tripartita Hufnagel, Bed. Mag. vol. iii. p. 414 (1766) (Berlin).
Mr. Oberthiir on p. 201, after Phytometra gumma,, mentions 3 species which
he considers of very doubtful occurrence in Algeria ; among them is Abrostola
triplasia. I have not received triplasia it is true, but I myself have captured
tripartita.
1 (J Environs d'Alger, May 6th, 1908 (W. R. and E. H.).
This species was overlooked by me.
The following are the doubtful species mentioned by Mr. Oberthiir in livr. i.
of his Etudes Entomologiques in 1876 as having been taken by Dr. Seriziat and
Mr. Gandolph and afterwards proved doubtful :
Cirphis comma (Linn.).
Abrostola triplasia (Linn.).
Phytometra chrysilis (Linn.).
Phytometra festucae Linn.
116 NOVITATES ZOOLOQICAE XXVII. 1920.
[Borolia sesamiodes Hmpsn.
Borolia sesamiodes Hampson, Cat. Lepitl. Phal. Brit. Mus. vol. v. p. 575. pi. xcv. £. 17 (1905)
(Hanirnani-es-Salahin).
I have never had this.
There are in the British Museum 4 (J^, 2 $ $ Hammam-es-Salahin, March —
April 1904-1906 (Lord Walsingham).
This species was overlooked by me.]
433. Pseudomecia lithoxylea (Bang-Haas).
Hypomecia Hlhoxylea Bang-Haas, Iris, vol. xxvi. p. 157. pi. vi. f. 19 (1912) (Batna).
1 (J October 1913 (V. Faroult).
The only specimen received at Tring of this species had been mislaid, and
so was omitted from its proper place in this article.
434. Miselia cappa (Hiibn.).
Noctua cappa Hiibner, Samml. Eur. Schmett. Xoct. f. 447 (1827).
The single specimen received was mislaid when the portion of the article
treating of the Miselias was being written. This appears to be the first record
for Algeria.
1 $ Sidi-bel-Abbes, May 1918 (M. Rotrou).
435. Epipsilia faroulti sp. nov.*
$. Uniform mouse-grey. Hindwings darker, with paler fringe and base.
Forewings with two obsolete black antemedian lines, orbicular with faint and
reniform with very pronounced black ring, 2 postmedian black lines, with row of
black dots between.
Length of fore wing, 18 mm. ; expanse, 42 mm.
1 $ El Mahouna, September 27, 1919 (V. Faroult).
This species is added here as it came to hand after the article had gone
to press.
The total number of species and subspecies of Noctuidae enumerated in this
paper as recorded from Mauretania is 471 and 4 doubtful records.
Mr. Oberthur records 337 and 3 doubtful ones. As, however, Mr. Oberthiir
follows Guenee's classification, he has omitted the Polygoninae and the genera
Sarrothripus, Nycteola, Earias, Hylophila, Rivula, and Parascotia, which are not
Noctuidae according to Guenee. If we deduct from my list the 14 species included
in these genera I have enumerated 457 species and subspecies as opposed to Mr.
Oberthiir's 337— an increase of 120. Of Mr. Oberthur's 337 there are 32 which I
do not possess or else have not received from Mauretania. Of the 471 I enumerate
there are altogether 36 either not in the Tring Museum or else not from Maure-
tania. Of the 441 species represented at Tring from Mauretania, the number
of examples is 30,691.
* All recent authors spell Hiibner's genus Epipsilia " Episilia," but the former spelling is that
of the author.
NOVITATES ZOOLOGICAE XXVII. 1920. 117
LIST OF SPECIES IN THE ORDER OF THE CATALOGUE OF
LEPIDOPTERA PHALAENAE IN THE BRITISH MUSEUM.
NOCTUIDAE.
Agrotinae.
1. Heliothis chanzyi (Oberth.).
2. Rhodocleptria incarnata (Freyer).
3. Chloridea dipsacea (Linn.).
4. Chloridea peltigera (Schiff. & Den.).
5. Chloridea nubigera (Herr.-Sch.).
6. Chloridea obsoleta (Fabr.).
7. Xylina delphinii darollesi (Oberth.).
8. Melicleptria scutosa (Schiff. & Den.).
9. Timora albida Hmpsn.
10. Erithrophaia canroberti Oberth.
11. Cladocerotis optabilis (Boisd.).
12. Euxoa obesa lipara (Ramb.).
13. Euxoa crassa (Hiibn.).
13a. Euxoa lata (Treit.).
14. Euxoa lasserrei (Oberth.).
15. Euxoa messaouda (Oberth.).
16. Euxoa noctambulatrix (Chret.).
17. Euxoa rugifrons (Mab.).
18. Euxoa capsensis (Chret.).
19. Euxoa segetum (Schiff. & Den.).
20. Euxoa vestigialis (Rott.).
21. Euxoa spinijera spinijera (Hiibn.).
22. Euxoa hoggari Rothsch.
23. Euxoa hastifera abdallah (Oberth.).
24. Euxoa mauretanica (B.-H).
25. Euxoa doufanae (Oberth.).
26. Euxoa powelli (Oberth.).
27. Euxoa robiginosa Stdgr.
28. Euxoa obelisca (Schiff. & Den.).
29. Euxoa radius radius (How.).
30. Euxoa radius erythroxylea (Treit.).
31. Euxoa oranaria (B.-H.).
32. Euxoa rotroui Rothsch.
33. Euxoa cos cycladum (Stdgr.).
34. Euxoa constanti (Mill.).
35. Euxoa eos (Oberth.).
36. Euxoa christophi (Stdgr.).
37. Euxoa trux (Hiibn.).
38. Euxoa tritici (Linn.).
l]g NOVITATES ZOOLOGICAE XXVII. 1920.
39. Euxoa distinguenda (Led.).
40. Euxoa bugeaudi bugeaudi (Oberth.).
41. Euxoa bugeaitdi islyana (Oberth.).
42. Euxoa cursoria (Hufn.).
43. Euxoa celsicola gueddelanea (Oberth.).
44. Euxoa kaaba (Oberth.).
45. Euxoa imperator (B.-H.).
46. Euxoa lucipeta (Schiff. & Den.).
47. Agrotis ypsilon (Rott.).
48. Agrotis orbona (Hufn.).
49. Agrotis comes (Treit.).
50. Agrotis pronuba (Linn.).
51. Agrotis norm Oberth.
52. Agrotis c. nigrum (Linn.).
53. Agrotis flammatra (Schiff. & Den.).
54. Agrotis leucogaster (Frr.).
55. Agrotis picata B.-H.
56. Agrotis nisseni Rothsch.
57. Agrotis xanthographa (Schiff. & Den.).
58. Agrotis auguroides Rothsch.
59. Agrotis praecipuina (Rothsch.).
60. Epipsilia simulatrix (Gey.).
61. Epipsilia faceta (Treit.).
62. Epipsilia straminea (Rothsch.).
63. Epipsilia lycoplwtioides (Rothsch.).
63a. Epipsilia faroulti Rothsch.
64. Lycophotia mansoura (Chret.).
65. Lycophotia agrotina (Rothsch.).
66. Lycophotia kermesina (Mab.).
67. Lycophotia margaritosa (Haw.).
68. Lycophotia photophila (Guen.).
69. Lycophotia ignipeta (Oberth.).
70. Epilecta linogrisea lutosa (Stdgr.).
71. Triphaena janthina algirica Oberth.
72. Triphaena janthina intermedia Rothsch.
73. Triphaena fimbria (Linn.).
Hadeninae.
74. Saragossa seeboldi arabum Oberth.
75. Scotogramma trijolii cinnamomina Rothsch.
76. Scotogramma chimaera Rothsch.
77. Scotogramma sodae rosacea Rothsch.
78. Scotogramma implexa (Hiibn.).
79. Miselia luteago (Schiff. & Den.).
80. Miselia peregrina (Treit.).
81. Miselia oleracea variegata (Aust.).
82. Miselia softa luteocinnamomea Rothsch.
82a. Miselia cappa (Hiibn.).
NOVITATES ZOOLOGICAE XXVII. 1920. 119
83. Miselia dysodea faroulti (Rothsch.).
84. Miselia se.re.na (Schiff. & Den.).
85. Miselia grisea (D. Lucas).
86. Miselia bicruris (Hufn.).
87. Miselia antitypina (Rothsch.).
88. Miselia carpophaga (Borkh.)
89. Miselia magnolii (Boisd.).
90. Miselia filigramma (Esp.).
91. Miselia conspersa (Schiff. & Den.).
92. Miselia compta galactina (Turati).
93. Luperina (Pacheira) leucophaea (Schiff. & Den.).
94. Pronotestra silenides (Stdgr.).
94a. Aglossestra mariae-ludovicae (D. Lucas).
95. Epia silenes (Hiibn.).
96. Epia cinochrea (Chret.).
97. Cardepia deserticola Hmpsn.
98. Cardepia irrisor mauretanica Rothsch.
99. Hadula pulverata (B.-H.).
100. Hadula griseola (Rothsch.).
101. Monima stabilis (Schiff. & Den.).
102. Monima critda (Schiff. & Den.).
103. Sideridis lithargyria argyritis Ramb.
104. Sideridis albipuncta (Schiff. & Den.).
105. Sideridis vitellina (Hiibn.).
106. Brithys pancratii (Cyr.).
107. Brithys encausta (Hiibn.).
108. Cirphis loreyi (Dup.).
109. Cirphis I. album (Linn.).
(Cirphis comma (Linn.)).
110. Cirphis riparia (Ramb.).
111. Cirphis algirica (Oberth.).
112. Cirphis sicula (Treit.).
113. Cirphis punctosa (Treit.).
114. Cirphis putrescent (Gey.).
115. Cirphis zeae (Dup.).
116. Cirphis unipuncta (Haw.).
117. Cirphis congrua (Hiibn.).
118. Borolia sesamiodes Hmpsn.
119. Leucania obsoleta (Hiibn.).
120. Leucania languida (Stdgr.).
Cucnlliinae
121. Copicucullia syrtana (Mab.).
122. Copicucullia oberthuri (Culot).
123. Cucullia chamomillae calendulae Treit.
124. Cucullia santolinae Ramb.
125. Cucullia scrophidariphaga Ramb.
120
NOVTTATES ZOOLOOICAE XXVII. 1920.
126. Cucullia blattariae (Esp.).
127. Cucullia scrophulariphila Stdgr.
128. Cucullia thapsophaga Treit.
129. Cucullia oberthuri Rothsch.
130. Cucullia verbasci (Linn.).
131. Cucullia beata Rothsch.
132. Cucullia biskrana.
133. Empusada argentina (Fabr.).
134. Lophoterges millieri (Stdgr.).
135. Hypomecia quadrivirgula (Mab.).
136. Copiphana gafsana (Blach.).
137. Cleophana chabordis Oberth.
138. Cleophana boetica diluta Rothsch.
139. Cleophana pectinicornis Stdgr.
140. Cleophana jubata Oberth.
141. Cleophana vaulogeri Stdgr.
142. Cleophana affinis Rothsch.
143. Cleophana fatima B.-H.
144. Cleophana diffluens mauretaniae Rothsch.
145. Cleophana versicolor Stdgr.
146. Cleophana mauretanica Stdgr.
147. Amephana warionis (Oberth.).
148. Amephana aurita (Fabr.).
149. Omphalophana serrata (Treit.).
150. Omphalophana adamantina (Blach.).
151. Omphalophana pauli Stdgr.
152. Omia cyclopea (Gras.).
153. Omia oberthuri Allard.
154. Metopoceras canteneri canteneri (Dup.).
155. Metopoceras canteneri pallidior Rothsch.
156. Metopoceras felicina (Lonz.).
157. Metopoceras khalildja Oberth.
158. Metopoceras otnar (Oberth.).
159. Metopoceras morosa Rothsch.
160. Ammetopa codeti Hmpsn.
161. Brachygalea albolineata (Blach.).
162. Calophasia stigmatica Rothsch.
163. Calophasia kraussi Rebel.
164. Calophasia almoravida Grasl.
165. Calophasia platyptera (Esp.).
166. Leucochlaena oditis (Hiibn.).
167. Leucochlaena scillae (Chret.).
168. Leucochlaena orana (Lucas).
169. Ulochlaena hirta (Hiibn.).
170. Bombycia chretieni (Rothsch.).
171. Bombycia angularis (Chret.).
172. Derthisa trimacula (Schiff. & Den.).
173. Aporophyla chioleuca (Herr.-Sch.).
174. Aporophyla nigra (Haw.).
NOVITATES ZOOLOQICAE XXVII. 1920. 121
175. Lithophane semibrunnea (Haw.).
176. Graptolitha lapidea ochreomacula Rothsch.
177. Axylia exsoleta (Linn.).
178. Dichonia areola mustapha (Oberth.).
179. Dryobota furva (Esp.).
180. Meganephria oxyacanthae (Linn.).
181. Agriopis aprilina bouveti (D. Lucas).
182. Eumichtis lichenea (Hiibn.).
183. Eumichtis solieri (Boisd.).
184. Eumichtis accipitrina (Esp.).
185. Eumichtis protect (Schifi. & Den.).
186. Eumichtis monochroma (Esp.).
187. Eumichtis roboris cerris (Boisd.).
188. Valeria oleagina (Schiff. & Den.).
189. Antitype rosea Rothsch.
190. Antitype hagar Rothsch.
191. Antitype sahariensis Rothsch.
192. Antitype flavicincta (Schiff. & Den.).
193. Antitype nigrocincta (Treit.).
194. Antitype dubia (Cup.).
195. Antitype discalis Rothsch.
196. Antitype germana Rothsch.
197. Antitype argillaceago deliciosa (Oberth.).
198. Antitype subvenusta Pungl.
199. Rhizotype flammea (Esp.).
200. Rhizotype crassicornis obscura (Oberth.).
201. Bryomima codeti codeti (Oberth.).
202. Bryomima codeti nisseni (Rothsch.).
202a. Dasysternum jaroidti Rothsch.
203. Dasythorax rotroui Rothsch.
204. Conistra vacinii sebdouensis (Aust.).
205. Conistra silene (Schiff. & Den.).
206. Conistra veronicae (Hiibn.).
207. Conistra erythrocephala (Schiff. & Den.).
208. Grammoscelis magnifica (Rothsch.).
209. Omphaloscelis polybela (de Joan.).
210. Omphaloscelis lunosa (Haw.).
211. Amathes ivitzenmanni (Standf.).
212. Amathes ruticilla (Esp.).
213. Amathes lychnidis (Schiff. & Den.).
214. Amathes haematidea (Dup.).
215. Amathes lota (Linn.).
216. Amathes macilenta (Haw.).
217. Amathes helvola (Linn.).
218. Amathes litura (Linn).
219. Amathes lucida (Hufn.).
220. Cymatophora algirica (Culot).
221. Xantholeuca croceago (Schiff. & Den.) (before Conistra).
222. Cosmia austauti (Oberth.).
j 22 Novitates Zoological XXVII. 1920.
Zenobiinae (Acronyctinae).
223. Pyrois effma (Boisd.).
224. Amphipyra pyramided (Linn.).
225. Amphipyra tetra (Fabr.).
226. Amphipyra tragopoginis distincta Rothsch.
227. Anthracia ephialtes (Hiibn.).
228. Mania maura (Linn.).
229. Parastichtis arabs arabs (Oberth.).
230. Parastichtis arabs standjussi (Turati).
231. Parastichtis arabs biskrae (Oberth.).
232. Parastichtis monoglypha (Hufn.).
233. Parastichtis spinosa (Chret.).
234. Trachea secalis (Linn.).
235. Euplexia lucipara leonhardi Rebel.
236. Procus faroulti (Rothsch.).
237. Procus furuncula (Schiff. & Den.).
238. Eremobia alpigena (Boisd.).
239. Sidemia aflouensis Rothsch.
240. Sidemia fulva (Rothsch.).
241. Pseudomecia lithoxylea (B.-H.) (correct place after Stilbina).
242. Margelana irritaria (B.-H.).
243. Centropodia inquinata Mab.
244. Pseudamathes volloni (D. Lucas).
245. Pseudopseustis tellieri (D. Lucas).
246. Pseudohadena chenopodiphaga (Ramb.).
247. Pseudohadena roseonitens (Oberth.).
248. Palluperina powelli (Culot).
249. Palluperina nickerlii graslini.
250. Palluperina dayensis (Oberth.).
251. Palluperina dumerilii (Dup.).
252. Trigonophora meticulosa (Linn.).
253. Eriopus latreillei (Dup.).
254. Eriopus juventina (Cram.).
255. Oedibrya subplumbeola (Culot).
256. Oederemia precisa (VVarr.).
257. Bryophila muralis (Forst.).
258. Bryophila pseudoperla Rothsch.
259. Bryophila aerumna Culot.
260. Bryophila bilineata Rothsch.
261. Bryophila albimaculata albimaculata Rothsch.
262. Bryophila albimaculata grisescens Rothsch.
263. Bryophila algae (Fabr.).
264. Bryophila receptricida pallida B. Baker.
265. Bryophila ravula (Hiibn.).
266. Bryophila maeonis Led.
267. Bryophila divisa oxybiensis Mill.
268. Bryophila simulatricula Guen.
269. Bryophila antias Culot.
Novitates Zoolooicae XXVII. 1920. 123
270. Bryophila anaemica Hmpsn.
271. Bryophila petraea Guen.
272. Iambiodes incerta Rothsch.
273. Polyphaenis xanthochloris graslini Culot.
274. Thalpophila vitalba (Fit.).
275. Sidemia fissipuncta oberthuri Rothsch. (correct place after 238).
276. Craniophora pontica (Stdgr.).
277. Acronycta tridens (Schiff. & Den.).
278. Acronycta psi (Linn.).
279. Acronycta rumicis pallida Rothsch.
280. Stilbina numida (Oberth..)
281. Prodenia litura (Fabr.).
282. Spodoptera abyssinia Guen.
283. Laphygma exigua (Hubn.).
284. Rabinopteryx subtilis (Mab.).
285. Rabinopteryx nelvai Rothsch.
286. Stilbia anomala calberlae (FaiLL).
287. Stilbia algirica (Culot).
288. Stilbia tnratii (D. Lucas).
289. Athetis atriluna Guen.
290. Athetis ambigua (Schiff. & Den.).
291. Athetis kadenii rufostigmata Rothsch.
292. Athetis flava (Oberth.).
293. Athetis approximans Rothsch.
294. Athetis clavipalpis (Scop.).
295. Athetis jacobsi Rothsch.
296. Athetis germaini (Dup.).
297. Athetis pertinax inumbrata Rothsch.
298. Athetis oberthuri Rothsch.
299. Athetis aspersa (Ramb.).
300. Athetis alsines (Brahm.).
301. Athetis blanda (Schiff. & Den.).
302. Athetis casearia (Stdgr.).
303. Athetis astigmata Rothsch.
304. Athetis hispanica (Mab.).
305. Athetis ingrata (Stdgr.).
306. Athetis flavirena (Guen.).
307. Athetis scotoptera (Piingl.).
308. Athetis euxoides Rothsch.
309. Athetis persimilis Rothsch.
310. Athetis distigma (Chret.).
311. Athetis halimi (Chret.).
312. Hydrilla caliginosa (Hubn.).
313. Proxenus bicolor (Chret.).
314. Hadjina viscosa (Frr.).
315. Catamecia mauretanica Stdgr.
316. Catamecia jordana balestrei (D. Lucas).
317. Nainangana chimaera Rothsch.
318. Hydroecia xanthenes orientalis (Oberth.).
124
Novitates Zoolooicae XXVU. 1920.
319. Enargia ulicis (Stdgr.).
320. Enargia regina (Stdgr.).
321. Enargia algirica (Culot.)
322. Enargia jordani Rothsch.
323. Arenostola deserticola Stdgr.
324. Arenostola mabillei (D. Lucas).
325. Oria fulva africana Oberth.
326. Archanara neurica (Hiibn.).
327. Archanara dissoluta (Hiibn.).
328. Archanara affinis Rothsch.
329. Sesamia vuteria (Stoll.).
330. Sesamia cretica Led.
331. Sesamia striata Stdgr.
332. Sesamia calamistis Hmpsn.
333. Simyra autumna Chret. (correct place after Stilbina).
334. Argyrospila musculosa (Hiibn.).
335. Argyrospila dulcis Oberth.
336. Argyrospila striata Stdgr.
337. Protomeceras mimicaria (Oberth.).
338. Synthymia fixa australis (Oberth.).
339. Azenia sabulosa (Rothsch.).
340. Aegle vespertalis (Hiibn.).
Erastriinae.
341. Catablemma geyri (Rothsch.).
342. Catablemma cremorna Rothsch.
343. Eublemma velox griseomargo (Warr.).
344. Eublemma lacernaria (Hiibn.).
345. Eublemma suava blandula (Ramb.).
346. Eublemma jucunda (Hiibn.).
347. Eublemma syrtensis Hmpsn.
348. Eublemma ostrina (Hiibn.).
349. Eublemma pseudostrina Rothsch.
350. Eublemma grata (Guen.).
351. Eublemma cochylioides (Guen.).
352. Eublemma parva (Hiibn.).
353. Eublemma candidana Fabr.
354. Eublemma scitula (Ramb.).
355. Eublemma permixla (Stdgr.).
356. Eublemma albida (Dup.).
357. Eublemma deserti Rothsch.
358. Eublemma purpurina (Schiff. & Den.).
359. Etiblenuna polygramma (Dup.).
360. Eublemma arida Rothsch.
361. Eublemma subvenata (Stdgr.).
362. Eublemma albidior Rothsch.
363. Eublemma albicans (Guen.).
364. Eublemma virginalis (Oberth.).
Novitates Zooloqicae XXVII. 1920. 126
365. Eublemma emir (C'ulot).
366. Eublemma deserta (Stdgr.).
367. Eublemma ernesti Rothsch.
368. Eublemma albivestalis Hmpsn.
369. Eublemma wollastoni N. C. Rothsch.
370. Eublemma lacteola Rothsch.
371. Eublemma pemivea Rothsch.
372. Eublemma croceus Rothsch.
373. Eublemma conjusa Rothsch.
374. Eublemma nelvai Rothsch.
375. Phyllo-phila numerica disjecta Warr.
376. Eulocastra diaphora (Stdgr.).
377. Nereisana oranaria (Lucas).
378. Crosia liachem Dupont.
379. Erastria trabealis deleta (Stdgr.).
380. Tarache lucida (Hufn.).
381. Tarache biskrensis (Oberth.).
Fhlogophorinae (Euteliinae).
382. Phlogophora adulatrix (Hiibn.).
Odontoninae (Stictopterinae).
383. Nycteola falsalis (Herr.-Sch.).
Sarrothripinae.
384. Sarrothripus revayana (Scop.).
Westermanniinae.
385. Earias insulana (Boisd.).
386. Earias chlorion Ramb.
387. Earias albovenosana Oberth.
388. Earias chlorophyllana Stdgr.
389. Hylophila africana Warr.
390. Xanthodes malvae (Esp.).
Catocalinae.
391. Mormonia dilecta powelli (Oberth.).
392. Mormonia sponsa laeta (Oberth.).
393. Catocala promissa hilaris Oberth.
394. Catocala optata sultana B.-H.
395. Catocala optata intermedia Hmpsn.
396. Catocala puerpera rosea (Aust.).
397. Catocala elocata (Esp.).
398. Catocala oberthuri Aust.
399. Catocala conjuncta vivida Warr.
400. Catocala conversa (Esp.).
126
NOVTTATES ZOOLOOICAE XXVII. 1920.
401. Catocala nymphaqoga vallantini Oberth.
402. Ephesia nymphaea (Esp.).
403. Ephesia eutychea (Treit.).
404. Minucia lunaris maura Oberth.
405. Anna tyrhaca (Cram.).
406. Parallelia algira (Linn.).
407. Grammodes stolida (Fabr.).
408. Grammodes boisdeffrei (Oberth.).
409. Grammodes geometrica (Fabr.).
410. Anydrophila sabourodi (D. Lucas).
411. Callistege (Cerocala) algiriae (Oberth.).
412. Callistege (Cerocala) sana (Stdgr.).
413. Leucanitis kabylaria B.-H.
414. Hyperglaucitis benenotata moses Stdgr.
415. Clytie sancta (Stdgr.).
416. Clytie luteonigra Warr.
417. Clytie arenosa Rothsch.
418. Clytie syrdaja Hmpsn.
419. Cortyta acrosticta (Piingl.).
420. Cortyta rosacea (Rebel).
421. Cortyta leucoptera (Hmpsn.).
Phytometrinae.
422. Phytometra ni (Hiibn.).
423. Phytometra daubei (Boisd.).
424. Phytometra chalcytes (Esp.).
425. Phytometra accentifera (Lef.).
(Phytometra festucae (Linn.)).
426. Phytometra gamma (Linn.).
(Phytometra chrysitis (Linn.)).
427. Phytometra orichalcea (Fabr.).
428. Abrostola tripartita (Hiifn.).
(Abrostola triplasia (Linn.)).
Noctuinae.
429. Anumeta atrosignata harterti Rothsch.
430. Anumeta sabulosa Rothsch.
431. Anumeta major Rothsch.
432. Anumeta cestis parvimacula Rothsch.
433. Anumeta hilgerti Rothsch.
434. Anumeta spatzi Rothsch.
435. Anumeta straminea (B.-H.).
436. Drasteria oranensis Rothsch.
437. Syneda caileno caileno (Lef.).
438. Syneda caileno philippina (Aust.).
439. Catephia leucomelas (Linn.).
440. Mageutica alchymista alchymista (Schiff. & Den.).
EXPLANATION OF PLATE XIV.
(Pages 102—104.)
Nos.
1. Catocala nymphagoga vallantini (Oberth.), $ Ain Tellout, 6.7.1917.
2-9 & 11. Catocala nymphagoga vallantini (Oberth.), 6 $$, 2 <j>$ Ain Draham,
July 1911.
12. Catocala nympJiagoga vallantini (Oberth.), 1 $ Sebdou, 17.7.1918.
13-15 & 17-24. Catocala nymphagoga vallantini (Oberth.), series of 6 q£, 5 $$
Ain Draham, July 1911, showing all intergradations from typical C. n.
vallantini to form with central band on hindwing and sharp pattern
on fore wing.
10 & 16. C. nymphagoga vallantini ab. griseola Warr., $ $ Ain Draham, July 1911.
25. C. nymphagoga nymphagoga Esp., <J Lorgono, Sardinia, July 1911.
26. C. nymphagoga nymphagoga Esp., <J Dalmatia.
27-28. C. nymphagoga nympJiagoga Esp., cj? Herculesfiirdo, July 1907.
29. C. n. nymphagoga ab. alternata Warr., $ Guittery, France.
30-39. C. n. vallantini Oberth., 3 £$, 6 §9 Ain Draham, showing variation,
July 1911.
NOVITATES ZOOLOGIC.-E. VOL. XXVII. ig20.
Pl. XIV.
E. S. Knight, pinx.
EXPLANATION OF PLATE XV.
Nos.
1. Eublemma permixta ab. mozabitica Rothsch., $ (type) Ghardaia, April
1911 p. 78
2. E. permixta ab. intermedia Rothsch., $ OuedNca, April 1914 - - p. 78
3. E. permixta ab. arenosa Rothsch., $ Oued Nca, April 1912 . p. 78
4. E. permixta ab. nivescens Rothsch., $ Sandana, S. of Ghardaia,
May 1912 - p. 79
5. E. permixta (Stdgr.), $ Ain Sefra, June 1915 . . . p. 78
0. Cleophana aftinis Rothsch., ? Guelt-es-Stel, April 1913 - - p. 68
7-8. Cleophana versicolor Stdgr., <J° Bou Saada, May 1911 . p. 70
9. Cleophana marocana Stdgr., Sebdou, Morocco - - - p. 70
10. Cleophana diffluens diffluens Stdgr., $ Chiclana, for comparison . p. 69
11. Cleophana diffluens mauretaniae Rothsch., Hammam-Meskoutine,
May 1914 p. 69
12. Cleophana diffluens lusitanica Culot, Caldas de Monchique, for
comparison . . . . . . . . . p. 70
13-15. Cleophana fatima B.-H., 1 <J, 2 $$ Gafsa (co-type, Tilghemt April
1912, Ghardaia 1911) p. 68
16. Cleophana boetica diluta Rothsch., <$ Bou Saada, May 1910 . p. 66
17. Cleophana boetica diluta Rothsch., $ Sebdou, May 1918 - p. 66
18. Cleophana boetica boetica Rmbr., J Caldas de Monchique, for com-
parison. . . . . . . . . . p. 66
19. Amephana warionis (Oberth.)X Cleophana boetica diluta Rothsch.,
Guelt-es-Stel, April 1913 p. 66
20. Metopoceras morosa Rothsch., q (tyPe) Guelt-es-Stel, May 1913 . p. 51
21. Ammetopa codeti Hmpsn., (J Oued Amra, N. of Ideles, May 1914 - p. 50
22-23. Bryomima codeti codeti (Oberth.), 2 JJ Ain Sefra May 1913,
Sebdou May 1918 . p. 50
24-25. Bryomima codeti nisseni (Rothsch.), cj$ Guelt-es-Stel, April
1912, May 1913 - - - - - - • - - - p. 50
26. Calophasia stigmatica Rothsch., <J between Ouargla and El Golea,
March 1912 p. 71
27-28. Leucochlaena orana (Lucas), (J$ Oudjda November 1914,
Perregaux November 1915- - - - - - -p. 23
29. Euxoa noctambulatrix (Chret.), <J Sidi Ferruch, Algeria . p. 23
NOVITATES ZOOLOOIC/E. VOL. XXVII. Ig20.
Pl. XV.
I-
t
\\^
%f#
^ "
**/m
iS
20
23
24
«i
26
Horace Knight^ pinx.
EXPLANATION OF PLATE XVI.
Nos
1.
2-3.
Iambiodes iticerta (Rothsch.), 1 $ Oued N9a, April 1914
Metapistis picturata (Rothsch.), $$ Arefidji, March 1912,
N9a, April 1914
Rabinopteryx nelvai Rothsch., $ Batna, 1913 — 1914 . .
Cucullia auceps Stdgr., <J Ganden Aschabad, for comparison
Cucullia oberthuri Rothsch., § El Kantara, May 1911
Cucullia beata Rothsch., $ (type) Sebdou, 1918 -
Athetis euxoides Rothsch., $ Batna .
Athetis persimilis Rothsch., <$ Souk-Ahras, April 1914 -
Antarchaea erubescens (B.-H.), $ Djebel Mekter, May 1913 .
12. Anumeta spatzi Rothsch., ^J Amgid, April 1914 -
Oued
4.
5.
6.
7.
8.
9.
10.
11-
13-14. Anumeta major Rothsch., <J$ Aln Talba May 1914, N. of El
Golea May 1912
15. Anumeta sabulosa Rothsch., (J Amgid, February 1914 -
16. Drasteria oranensis Rothsch., <$ Ain Sefra, May 1913 .
17. Cortyta rosacea (Rebel), <J Oued Dehin, March 1914 -
18. Eublemma arida Rothsch., <J (type) El Golea, May 1912
19. Eublemma crocea Rothsch., $ Ain Tahart, April 1914 -
20. Eublemma pernivea Rothsch., $ Ain Sefra, August 1915
21-22. Eublemma scitula (Ramb.), (J$ Sidi-bel- Abbes, August 1916
23. Catablemma geyri Rothsch., $ Tahihout, April 1914
24. Eublemma nelvai Rothsch., $ (type) Batna, 1913 — 1914
25. Eublemma pseudostrina Rothsch., (J Guelt-es-Stel, August 1913
26. Eublemma deserti (Rothsch.), ^ Ain Taiba, May 1914 -
p. 76
p. 71
p. 64
p. 62
p. 62
p. 62
p. Ill
p. Ill
p. 109
p. 95
p. 95
p. 95
p. 97
p. 93
p. 83
p. 84
p. 84
p. 76
p. 77
p. 112
p. 80
p. 79
NOVITATES ZoOLOGICE. Vol. XXVII. I920.
Pl. XVI.
w^Hgm
v
19
■
20
21
15 v«f
22
- *7I
'l/. />I»I.V
EXPLANATION OF PLATE XVII.
Nos.
1. Antitype hagar Rothsch., <J (type) Bou Saada, April 1911 . p. 53
2 & 3. Cardepia deserticola Hmpsn., <J Bou Saada May 1910, <J Colomb
Bechar April 1912 - - p. 57
4. Cardepia irrisor (Ersch.), $ Uralsk, May 1906, for comparison . p. 57
5. Cardepia irrisor mauretanica Rothsch., <J El Mesrane, June 1913 - p. 58
6. Scotogramma chimaera Rothsch., $ (type) Ain Sefra, March 1915 . p. 57
7. Miselia Sofia luteocinnamomea Rothsch., <J El Kantara, April 1911 p. 110
8. Miselia antitypina (Rothsch.), £ (type) Guelt-es-Stel, April 1913 . p. 48
9. Agrotis praecipuina (Rothsch.), (J Sidi-bel-Abbes, September 1917 - p. 37
10. Epipsilia straminea (Rothsch.), <J (type) Guelt-es-Stel, October
1912 p. 42
11. Euxoa rotroui Rothsch., 1 $ (type) Sidi-bel-Abbes, May 1918- - p. 29
12. 13, 14. Euxoa hoggari Rothsch., 1 <J, 2 $$ Oued Abou, S. Sahara,
January 1914 . . . . . . . . p. 27
15, 16. Euxoa spinifera hodnae (Oberth.), <J$, for comparison - p. 26
17. Agrotis auguroides Rothsch., <J Guelt-es-Stel, April 1912 . p. 36
18. Agrotis nisseni Rothsch., $ Guelt-es-Stel, October 1913 - - p. 36
19. Lycophotia kermesina ab. flavida Culot, <J Guelt-es-Stel, October
1912 p. 16
20,21. Sidemia fulva (Rothsch.), cj? El Mesrane, November 1913 - p. 44
22. Dasysternum faroulti Rothsch., $ (type) El Mesrane, November
1915 p. 45
23. Dasythorax rotroui Rothsch., $ (type) Messer, September 1917 - p. 45
24. Natnaugana chimaera Rothsch., $ (type) Environs Taourirt,
July 1918 p. 45
25. Sidetnia aflouensis Rothsch., (J (type) Aflou, October 1916 - - p. 45
26. Athetis oberthuri Rothsch., ^ (type) S. Oued Mya, April 1912. . p. 18
27. Euargia jordani Rothsch., $ (type) South Ahras, April 1914- - p. 41
28. 29. Epipsilia lycophotioides (Rothsch.), 2 ^ (types of inconspicua
Rothsch. and lycophotioides Rothsch.), Guelt-es-Stel, October 1912 p. 37
NOVITATES ZOOLOUIC/E. VoL. XXVII. I92O.
Pl. XVII.
Horace Knight, pinx.
NOVTTATES ZOOLOQIOAE XXVII. 1920. 127
441. Magevtica alchymista uniformis (B.-H.).
442. Acrobyla panacearum distincta Rothsch.
443. Metapistis picturala (Rothsch.).
444. Lipatephia eremophila (Reb.).
445. Acontia luctuosa (Schiff. & Den.).
446. Pandesma anysa distincta Rothsch.
447. Pandesma anysa sennarensis (Feld. & Rog.).
448. Raphia hybris (Hiibn.).
449. Tathorhynchus exsiccata (Led.).
450. Apopestes spectrum maura Warr.
451. Autophila maura (Stdgr.).
452. Autophila ligaminosa (Evers.).
453. Autophila dilucida libanotica (Stdgr.).
454. Autophila cerealis rosea (Stdgr.).
455. Rivula sericealis distincta Rothsch.
456. Scoliopteryx libatrix (Linn.).
457. Zethes insularis Ramb.
458. Parascotia nisseni Turati.
459. Antarchaea viridaria (Clerck).
460. Antarchaea sanctiflorentis aurantiacus Rothsch.
461. Antarchaea erubescens (B.-H.).
Polypogoniuae (Hypeninaei.
462. Nodaria cornicaiis (Fabr.).
463. Hypena obsitalis (Hiibn.).
464. Pechipago (Zanclognatha auct.) crinalis (Treit. ).
465. Pechipago {Zanclognatha auct.) flavicrinalis Rothsch.
466. Ophiuche lividalis (Hiibn.).
The 4 species without numbers and in brackets are the 4 whose record is
dubious.
128 NOVITATES ZOOLOGICAE XXVII. 1920.
THE BIRDS OF THE COMMANDER ISLANDS.
By Eenst Hartert, Ph.D.
THE Commander or Kommandorski Islands consist of two islands, Bering
Island, the larger, and Copper (Mednij) Island, the smaller of the two. They
are of special interest, as being the easternmost islands of the "Old World" in
the north. It is natural that, considering how closely Tschuktschenland and
Alaska on the one, the Commander and Aleutian Islands on the other hand,
approach each other, a number of birds, even some land-birds, are common
to both easternmost Asia and westernmost America, i.e. Alaska and the islands
in Bering Sea. Nevertheless there is a very marked difference between their
ornis, the bulk being distinctly palaearctic or nearctic.
The literature on the birds of the Commander Islands is not large, but
Stejneger's " Results of Ornithological Explorations in the Commander Islands
and in Kamtschatka " (Bull. U.S. Nat. Mus. No. 29, 1885), with its valuable
" Conclusions " and excellent plates, together with his Revised Catalogue of the
Birds inhabiting the Commander Islands (Proc. U.S. Nat. Mus. 1887) are far
better than a host of articles ; they may almost be called classical ornithological
literature, and nearly exhaust the subject. Besides these writings there is the
" Liste des oiseaux du Kamtschatka et des iles Commandores," by Dybowski
and Taczanowski, in the Bull, de la Soc. Zool. de France for 1884, pp. 145-61, a
mere " Liste " with localities.
Then there is a recent article based on Mr. Sokolnikoff's collections made
on the two islands 1907-1909, in Russian (!) in the Annuaire du Mus. Zool. Acad.
Imp. Sciences de St. Petersbourg" xiv. (" 1909"), Memoires, pp. 48-76, entitled
(in translation), " Short Outline of the Avifauna of the Commander Islands."
It adds seven species to Stejneger's list — but Rhodostethia rosea, had already
afterwards been added by the latter.
The most recent article known to me is, however, S. Buturlin's " Les
oiseaux de l'ile Mednij, de la grouppe Comander " (sic!) in Ornithol. et Avi-
culture, Moscow, iv. livr. 2, No. 41, 1913. It contains a list of 59 species,
one of which had not before been recorded from the group, and several
others not from Copper Isle. It appears to be a careful, up-to-date work,
but is written in Russian !
Besides these articles dealing with the birds of Bering and Copper Islands,
they are mentioned in other writings, chiefly in Taczanowski' s great work,
Faune Ornithologique de la Siberie Orientate," and, indeed, already a few by Pallas
( 1 827) ! Pallas's statements were taken from the MS. of Steller, who was wrecked
on Bering Island in 1741. From his notes Pallas described the now extinct
Phalacrocorax perspicillatus. At that time they were abundant, and to a great
extent Steller' s party lived on their flesh ; they were preferred to other Cor-
morants on account of their size, as one was an ample meal for three hungry
sailors. Steller' s men, however, did not exterminate the species, as a hundred
years after, the Governor of Sitka, Kuprianoff, did not find it rare, and collected
the few specimens known in the Museums of Petrograd, Leiden, and London.
Novitates Zoolooicae XXVII. 1920. 129
As this Cormorant is described as very stupid and was much persecuted, it
is generally supposed that it has been exterminated by men. This may be, but
it is perhaps as likely that it was finally wiped out by an epidemic disease, such
as took place in the winter of 1876 — 1877, when many thousands of Phalacrocorax
pelagicus were destroyed and masses of the dead birds covered the beach all
round the islands. The inhabitants of the islands, however, asserted that it
had last been seen about 1852 or so.
The almost complete collection made by Stejneger (about 2,000 specimens)
is in the Museum of the Smithsonian Institution in Washington, U.S.A.
About the same time as Stejneger the Polish explorer Dybowski made a
collection on the islands, and his skins are in the Warsaw Museum, and the
Governor, N. Grebnitski, collected birds which he sent to Stejneger and other
ornithologists.
Mr. N. Sokolnikoff, having held an official position on the Islands for a
number of years, collected for the Petrograd Museum. His first collection is
the one on which Bianchi based his article in 1909. The second collection, the
one on which the following article is written, consisting of over 860 skins, was
also intended for the Museum at Petrograd, but delivery being impossible, and
the collection slowly deteriorating in the climate and under the conditions it
was kept, Sokolnikoff offered it to the British Museum, who did not accept, and
passed the offer on to Lord Rothschild, who bought the birdskins.
As the above list shows, we have received 152 forms of birds from Mr.
Sokolnikoff.
21 forms known to have occurred we did not receive.
23 were obtained for the first time on the islands.
Stejneger's list (1887) had 143 species and subspecies.
Bianchi's of 1909 contained 153, of which 5 were quite doubtful.
Sokolnikoff's last collections confirmed 2 of Bianchi's doubtful ones and
added 21 others to the list, which thus consists of —
171 forms.
1. Podiceps griseigena holboellii Reinh.
<J ad., Bering Island, 21 .v. 1916.
cJ in winter plumage, Bering Island, 16.xi. 1909.
9 juv. in moult, 4.x. 11 (year ?), 31.x. 1912, 30. ix. 1911, Copper Island.
Stejneger says it " does not appear at the islands except as a straggler."
This is confirmed by the present collection, though the date of 21 .v suggests a
breeding- place not far away.
2. Podiceps auritus (L.).
2 winter birds, evidently in their first year. Rare straggler, according to
Stejneger.
3. Colymbus adamsii Gray.
cJ ad., Bering Island, 11. v. 1912.
^ juv., Copper Island, 11. xi. 1910.
Stejneger calls the White-billed Diver a winter visitor of rather rare
occurrence, and he obtained one and saw another.
9
130 Novitates Zoolooicae XXVTI. 1920.
4. Colymbus stellatus Pontopp.
Fine adult specimens were obtained on Bering and Copper Islands in spring
and summer, and 1 juv. in November on Copper Island. It breeds frequently
on the islands and appears, according to Stejneger, about the first of May.
5. Colymbus arcticus viridigularis (Dwight).
Garia viridigularis Dwight, Avk 1918, p. 198 (N.E. Siberia and western Alaska. Type N.E. Siberia)
S ad., Bering Island, 22. v. 1914.
? juv., Bering Island, 26.x. 1911.
c? ad., Copper Island, 12. vi. 1911.
cJ in winter plumage, Copper Island, 20. xi. 1910.
This species, judging from the dates, might possibly be breeding, but if so
it must be very rare.
(Bianchi enumerates Colymbus immer Brunn as an exceptional visitor.)
6. Una lomvia arra (Pall).
Several adult spring and summer specimens.
An adult winter bird and a number of young ones in various stages. Also
some eggs, but without indication of parents.
Uria lomvia arra breads in great numbers on the islands, but among them
Uria troille calijornica occurs sparingly !
U. 1. arra is very similar to U. I. lomvia, but generally a little larger (not
smaller as stated in the Cat. B. Brit. Mils.), the bill often stronger, thicker, but
shorter, sometimes, however, very long.
(Mr. Sokolnikoff did not send any U. troille calijornica.)
7. Uria columba columba (Pall.).
A number of adult and young from April to October. If the dates are correct
the spring moult is rather irregular, as a female from April 20th is in full black
summer garb, another from the same date has still a good many white feathers
left, while yet another (all females) from May 11th is chiefly white underneath,
though the black feathers are appearing everywhere. The change to the winter
plumage takes place in October.
The wings of the Bering Isle specimens are only 174 to 177 mm., but one
from Copper Island has wings of 1 82 mm.
Abundantly breeding.
(Uria carbo (Pall.) was observed in two pairs by Stejneger.)
8. Brachyrhamphus marmoratus perdix (Pall.).
A single male was obtained on May 11th on Copper Island. Since this
form breeds on Kamtchatka and the Kuril Islands its occurrence on the Com-
mander Islands, though not previously recorded, is not strange.
NOVITATES ZOOLOGICAE XXVII. 1920. 131
9. Synthliborhamphus antiquus (Gm.).
A series from both islands, the latest date being September 27th. Breeds
on both islands.
10. Aethia pygmaea (Gm.).
(Simorhynchus pygmaeus auct.)
Both islands, mostly from the autumn and winter months, but one from
May, and a few summer specimens. Breeding on both islands.
11. Aethia cristatella (Pall.).
(Simorhynchus cristatellus auct.)
Though regularly breeding (at least during Stejneger's stay there) on both
islands, Sokolnikofl only sent three adult winter birds and one young shot
October 28th, 1912.
12. Aethia pusilla (Pall.)
(Simorhynchus pusillus auct.)
A number of specimens from Bering Island from the winter months, in the
spring as late as May 10th, 1912. A female was also obtained on Copper Island
on April 17th, 1911. — No proof of the breeding of this Auklet on the Commander
Isles has yet been obtained.
13. Phaleris psittacula (Pall.).
Obtained on both islands in June and July. A young in down on Bering
Island, 20.vii. 1912. The down of the upperside, sides of head, neck, and body
and throat sooty, lighter at base, breast and abdomen greyish white.
(Cerorhinca monocerata was obtained by Grebnitzki, but neither Stejneger
nor Sokolnikoff came across it.)
14. Lunda cirrhata (Pall.).
Several fine adults and young from the autumn months. None in winter
plumage. According to Stejneger " occasionally, after severe gales, a few
specimens are found cast up on the beaches."
15. Fratercula corniculata (Naum.).
Several summer and autumn examples. In a female shot 24.x. 1910 the
basal plates have already fallen off.
16. Sterna paradisaea Briinn.
(Sterna macrura or arctica auct.)
cj? ad., Bering Island, 24. vi. 1915.
$ juv., Bering Island, 24. v. 1914.
Breeds on the islands (Stejneger. p. 85).
The adult S has quite an extended black tip to the upper mandible ! This
is very rare in paradisaea, but it does exist sometimes.
132 Novitates Zoolooicae XXVII. 1920.
17. Sterna longipeanis Nordm.
9 ad., Bering Island, 21. v. 1911.
<?<J ad., Bering Island, 9.vi.l912, 29. v. 1914.
Stejneger (p. 85) says that formerly he was wrong in giving it as breeding
on Bering Island. The dates of Sokolnikoff s specimens, however, suggest the
possibility, nay probability, of this species nesting on Bering Island.
The name camtschatica Pall, is doubtful and cannot be accepted for this
species.
18. Sterna aleutica Baird.
(?, Copper Island, 7.ix.l911.
This bird, though known to have occurred on the Siberian coast, and said
to have been found in Japan, is a new record to the Islands.
19. Larus glaucescens Nauru.
A magnificent series collected in the spring and summer months, and an
adult female shot December 26th, 1911.
This species is commonly breeding on both islands, and occurs in small
numbers throughout the year. In the Bull. Soc. Zool. France, 1884, p. 147,
Dybowski and Taczanowski mention this Gull as Larus glaucus (cf. Taczanowski,
Faune Orn. Siberie orient, ii. 1019), while their " Larus borealis " was, according
to Taczanowski, t.c. i. p. 1030, " Larus cochin-nans," but I consider all the
eastern Herring-Gulls east of the Taimyr Peninsula to be vegae.
20. Larus argentatus vegae Palmen.
A fine adult $ was shot on Copper Island, 9. vi. 1914, and four young birds
were obtained in May and June of various years, both on Bering and
Copper Islands.
21. Larus hyperboreus Gunn. 1767.
(Larus glaums Briinn. 1764, nee Pontopp. 1763.)
Two adult, male and female, and two juvenile specimens were shot on
Bering Isle in April, and another young in November. The adult male has the
upperside darker, more bluish, the female lighter, almost whitish.
This species had not yet been found on the Commander Islands, but as it
breeds in the high north and migrates down south to Japan, its occurrence there
was to be expected.
22. Larus schistisagus Stejn.
$ad., Bering Island, l.i.1911.
c??ad., Bering Island, 13. iv., 17. iv., 17. iv., 16. v. 1912.
$ ad., Copper Island, 12. vi. 1911.
cj 9 Juv., Bering and Copper Islands, October.
From these dates it appears as if the species might possibly breed on the
islands, though Stejneger said it did not.
NOVITATES ZOOLOQICAE XXVII. 1920. 133
23. Larus canus major Midd.
Lotus canus L. var. major Middendorff, Sibirische Reise, Zool. ii. 2. p. 243, Taf. xxiv. fig. 4 (1853 —
Stanow6y Mountains to Sea of Ochotsk).
3 ad., Copper Island, 26. v. 1912.
$ ad., Copper Island, -l.vi.1911.
c? juv., Copper Island, 23. v. 1911.
4(J? med. aet., Bering and Copper Islands, May and June.
2 juv., Bering and Copper Isles, September 1911.
All these birds belong undoubtedl}- to the large eastern form of the Common
Gull. The May and June dates of perfectly adult birds suggest the possibility
of their breeding on Copper Island, though during Stejneger's visit they seem
not to have done so.
24. Larus canus brachyrhynchus Rich.
Two young birds shot on Bering Island, 25. i. 1911, and Copper Island,
9.ix.l911, are so much smaller than all L. c. major that they must belong to
brachyrhynchus, which might very well occasionally visit the islands from North-
western America. Also Stejneger got one small specimen, which he called canus,
but if brachyrhynchus is separated from canus, these specimens must belong to
the former.
25. Larus ridibundus sibiricus But.
Larus ridibundus sibiricus Buturlin, Mess. Orn. ii. p. 66 (1911 — Kolyma Delta and Ussuri Land.
In Russian !).
3 adult summer birds without dates.
<$ ad., Bering Island, 19. v. 1915.
2 ad., Copper Island, 11. v. 1910.
cJ ad., Bering Island, 12. v. 1912.
<J nearly ad., Bering Island, 5. v. 191G.
$ juv., Bering Island, 9.xi.l912.
2 nearly ad., Bering Island, 19. v. 1916.
These specimens differ from most European birds shot about the same time
of the year by somewhat darker, less coffee-brown heads of the adult ones, longer
bills, and generally longer wings. The bill is 37-40 mm. long (from end of
feathering on culmen), the wing is about 315 to 321 mm., while the bill in European
specimens measures generally 29-36, the wing 302-310, very seldom to 315 and
317 mm. The brown of the head in a specimen from Lombardia, Italy, is just
as dark, and the same may be said of one from Mogador, Marocco, shot in March,
by Riggenbach. The bill of the Lombardian bird is also very long, i.e. 39 mm.
When Buturlin described his sibiricus he mentioned that it had a darker
grey upperside, that the outer web of the fifth primary was always grey, and the
dimensions larger, especially those of the tarsus. The strikingly longer bill is,
however, not mentioned. The back of our Commander Islands birds is not at
all darker, nor is the constantly grey colour of the outer web of the fifth primary
a character, as it is mostly grey — though not rarely partially white — in European
specimens. Japanese skins without date have the elongated bill, but their
wings are rather short.
Lena River specimens have the short bills of European examples and the
134 NO.ITATES ZoOLOGICAE XXVII. 1920.
wings as a rule no longer than the latter, but their heads are very light, though
summer birds in Europe have them very often equally pale. They would belong
to " Chroicoceplialus ridibundus lavrovi " Zarudny, Mess. Orn. iii. pp. 29, 30 (1912),
from Chirchik, Syr-Darya and Semiretchye, separated because they had lighter
heads, and, if I had a correct translation of the Russian description, are found
among darker- headed specimens. I do not consider this form separable, and
treat " lavrovi " as a synonym of Larus ridibundus ridibundus. The easternmost
form is apparently separable, but its distribution as yet very uncertain.
Stejneger did not meet with this bird on the islands, though he found it
nesting in Kamtchatka. The dates of Sokolnikoff's specimens suggest the
possibility of its breeding nowadays on the islands. Bianchi added ridibundus
to the list of Bering Island birds, as not breeding.
26. Larus gelastes Keys. & Bias.
An adult male, with the greyish black spots of the winter plumage behind
the eyes and ear-coverts, was shot on Copper Island, 7.x. 1912. The inner web
of the first primary has a wide slate-coloured inner margin. This is probably
a remainder of the juvenile plumage, but very unusual.
No Larus gelastes has ever been found so far east ; in fact, I do not know of
a record further east than Issik-Kul and Karachi.
27. Xema sabinii (Sabine).
cJad., Bering Island, 16. v. 1913.
Stejneger did not come across this species, nor was it obtained before by
Sokolnikoff.
28. Rhodostethia rosea (Macg.).
cf ad., Bering Island, S.xii. 1911.
? juv., Bering Island, 13. iii. 1914.
<J juv., Bering Island, 9.xii. 1915.
Stejneger in 1887 had no evidence of the occurrence on the islands, but
in the Auk, 1898, p. 183, he recorded a specimen collected by Grebnitski on
Bering Island, 10. xh. 1895.
29. Rissa tridactyla pollicaris Stejn.
This common breeding bird of the two islands, where opportunity for nesting
exists, was obtained in summer and winter.
In the young of all forms of Rissa the shorter secondaries are nearly quite
white, only with a grey patch towards the base of the outer web, a striking
peculiarity not mentioned in the Cat. B. Brit. Mus.
30. Rissa brevirostris Bruch.
c?$ ad., Bering Island, 7. v. 1912.
$ juv., Copper Island, 24. vi. 1911.
Breeding on both islands.
NOVITATES ZOOLOGICAE XXVI:. 1920. 135
31. Stercorarius pomarinus (Temm.).
$ ad., Bering Island, 3.vi.l912.
$ semi ad., Copper Island, 1 1 . vii. 1913.
Mentioned by Dybowski as occurring on Bering Island, but Stejneger did
not come across it.
32. Stercorarius longicaudus Vieill.
(?$ad., Bering Island, 4.vi.l911, 3.vi.l913.
According to Stejneger, " an occasional, though by no means uncommon "
visitor to the islands during migrations. The occurrence in June suggests the
idea of a breeding-place not far away.
33. Stercorarius parasiticus (L.).
{Stercorarius crepidatus in the Cat. B. Brit. Mus. xxv. p. 327, where the
nomenclature is arbitrary.)
4 adults with white underside, 3 with dark, from Bering and Copper Islands
in spring and summer. Stejneger called the light phase comparatively rare.
Also a young bird from Bering Island, 4 . viii . 1911.
34. Fulmarus glacialis rodgersii Cass.
(Fulmarus glacialis glupisha Stejn.)
This bird breeds in large colonies on both islands. Sokolnikoff sent a fine
series. Six belong to the dark form, C to the white one with more or less grey
mantle. One from Bering Island, date unreadable, has whitish grey, very faded
feathers on the back, while fresh feathers of a slaty grey colour come in ; most
feathers of the underside are grey with whitish tips, some fresh ones, however,
are quite grey. Another example, a bird of the year, Copper Island, 1.x. 1912,
is pure white all over.
35. Puffinus tenuirostris tenuirostris (Temm.).
Six specimens from both islands, collected from April to June 18th. There
can, judging by these dates, be hardly any doubt that this Petrel nests on the
islands, and it is a pity that the habits have not been recorded, nor any eggs sent.
Bianchi recorded it as nesting on both islands !
36. Oceanodroma furcata (Gm.).
Specimens from Bering Island in spring and winter, and from Copper Island,
where it breeds, in spring and winter.
37. Oceanodroma leucorrhoa leucorrhoa (Vieill.).
One male, Copper Island, 6. vii. 1911. Stejneger found it breeding at
Tchornij Mys., Copper Island.
{Diomedea albatrus occurs not rarely in the sea surrounding the islands, but
we did not receive specimens.)
(Haematopus ostralegus oscidans Swinh. is an occasional visitor, but we did
not receive specimens.)
136 Novit;<tes Zoologicae XXVII. 1920.
38. Arenaria interpres interpres (L.).
Several adult males from Bering Island, May and June 3rd, and young
in September.
It has not been proved to nest on the islands.
39. Squatarola squatarola hypomelaena (Pall.).
Two juvenile, September and October, Bering Island.
Though there is some overlapping, the larger bill and generally longer wing
of the eastern race cannot be denied, and therefore this subspecies should be
recognized.
40. Charadrius dominicus fulvus Gm.
A large series from both islands in May and autumn, the latest spring date
being May 30th.
41. Charadrius mongolus mongolus Pall.
A fine series of adult birds, both islands, from May and June, a pullus (Copper
Island), July 27th, unfortunately already covered with many feathers.
The black line separating the rufous chest from the white throat is often
entirely absent, or only indicated.
One juv. in first autumn plumage, September.
42. Charadrius alexandrinus alexandrinus L.
?, Bering Island, 21 .xi. 1911.
The occurrence on Bering Island is extraordinary, as the species is not a
northern one, though it extends eastwards to Corea.
43. Gallinago gallinago raddei But.
Scolopax (Gallinago) gallinago raddei Buturlin, Kuliki Rossieskoi Imperic-Premiya-k-Journal, in
Psovaia i Ruzheinaia Okhota, 1912, p. 54 of the separate copy. (Breeding in E. Siberia.
Russian !)
Taczanowski said that the majority but not all Snipes in East Asia differed
by having wider pale stripes and more rusty spotting on the upperside. less spotted
jugulum, and wider sincipital line, also less spotted, more white axillaries and
under wing-coverts. Buturlin named this form as above. Comparing eastern
and European Snipes, it is obvious that no colour differences are of any constancy
or found in the majority of specimens, but entirely individual, except the less
spotted jugulum which is observable in the great majority of eastern Snipes,
while such specimens, with almost uniform, less spotted jugulum are rare in
Europe. Moreover, there is a tendency in eastern birds to have smaller di-
mensions. European Snipes have wings of 129-140, females generally larger,
135-140, males 129-136, exceptionally 127-128 only. Eastern Snipes have
wings of 125-137, usually about 132, quite exceptionally to 140 mm. The wings
of 12 snipes from Bering and Copper Islands measure 126-133, once 136 ; those of
as many from the Tring Reservoirs 132 to 138 mm.
NOVTTATES ZOOLOQICAE XXVII. 1920. 137
It is therefore advisable to tentatively recognize Gallinago gallinago raddei,
though its characters are unstable and its distribution not yet certain.
The Snipe is a common breeding-bird on Bering Island. Sokolnikofi collected
specimens throughout the month of May.
44. Gallinago solitaria Hodgs.
GaUinaijo solitaria Hodgson, Gleanings in Science, iii. p. 238 (1831 — Nepal).
?, Copper Island, 10.x. 1910.
(J, Bering Island, 27.xii.1911.
This species has not previously been recorded from the Commander Islands,
but as it breeds from the Altai and Turkestan to Kamtchatka, its occurrence
is not unexpected, only the December date is extraordinary.
45. Erolia maritima quarta subsp. nov.
5 <J$ ad., May, Bering and Copper Islands.
9 ad., Copper Island, 2.ix. 1911, changing from summer to winter plumage.
9 <J $ in winter plumage from both islands, collected in November, December,
and March.
The Purple Sandpiper of the Commander Islands differs from E. m. couesi
from Alaska and the Aleutian Islands as follows '•
In the winter plumage the foreneck and jugulum are darker slate-colour
and less mixed with white. In the full summer plumage the edges to the feathers
of the upperside are much wider and of a brighter ferruginous, so that the upper-
side looks quite rust-red, with mostly concealed black centres to the feathers.
The wings measure 121-127, in one $ even 130 mm.
Type: <J, Bering Island, 11. v. 1912. N. Sokolnikofi leg.
We know from Stejneger that this species is resident on Bering Island, but
he says that some retire to more hospitable shores during the winter months.
46. Erolia acuminata (Horsf.).
5 autumn birds, September and October, both islands, where they are
autumn migrants.
47. Erolia maculata (Vieill.).
Tringa maculata Vieillot,iVowt>. Diet. d'Hist.Nat. xxxiv. p. 46.5(1819 — West Indian Islands or southern
U.S.).
(Erolia maculata is the correct name for the "Pectoral Sandpiper," often
called " Tringa pectoralis.")
cJ?, Bering Island, 6, 10, 18. ix. 1911.
Though only once recorded from the Commander Islands, byButurlin, 1913,
it is not unexpected that this species passes through on migration. Where these
birds winter is not yet known ; American examples migrate as far south as
Peru, Chile, and Argentina.
138 Novitates Zoolooicae XXVII. 1920.
48. Erolia temminckii (Leisl.).
2 2 ad., Bering Island, 26, 29. v. 1912.
Somewhat rare on passage.
49. Erolia subminuta (Midd.).
4 adult specimens, Bering Island, March, May, July ; Copper Island,
25. v. 1912.
According to Stejneger mainly on passage, but a few stay over the summer,
probably breeding.
Bianchi, in fact, gives it as breeding, probably from notes by SokoLnikoff.
50. Erolia ruficollis (Pall.).
3$ ad., Bering Island, 25. v. 1914, 25. v. 1915, 25. vi. 1914.
According to Stejneger only on migration, but the late date in June suggests
the possibility of its nesting.
51. Erolia alpina sakhalina (Vieill.).
<J9ad., Copper Island, 13. v. 1912; Bering Island, 2.vi.l914, 24. vi. 1914,
25. vi. 1914.
According to Stejneger only on passage. The late dates of these birds
suggest the possibility, but do of course not prove their breeding on the islands.
52. Erolia ferruginea (Briinn.).
<J ad., Bering Island, 2.vi.l916.
2 ad., Copper Island, 12.x. 1910.
This species has not yet been recorded from these islands.
(Erolia tenuirostris = crassirostris, mentioned by Bianchi as doubtfully
nesting, was not sent by Sokolnikoff to us.)
53. Eurynorhynchus pygmeus (L.).
Plalalea pygmea Linnaeus, Syst. Nat. ed. x. i. p. 140 (1758 — " Surinam " ! Errore !).
2 ad., Bering Island, 5.ix.l911.
Not previously recorded from the islands.
("Calidris armaria" now to be called Crocethia alba (Pall.), was met with
by Stejneger — one out of a flock shot.)
54. Limosa lapponica baueri Naum.
17 specimens throughout May and as late as June 2Gth, mostly with cinnamon
underside, but some from the same days still white and barred.
Though, Stejneger says, some individuals stay over summer, they were not
nesting.
NOVITATES ZOOLOGICAE XXVII. 1920. 139
55. Limosa limosa melanuroides Gould.
5 (J$ in fine nuptial plumage, obtained May 20th to 26th (mostly 1913),
on Bering Island ; one (not sexed) with very little rufous colour, Copper Island,
7.vi.l911.
According to Stejneger a very rare visitor, as only one specimen was known
to him.
56. Tringa nebularia (Gunn.).
(Totanus nebularius, Glottis nebularius, Totanus glottis auct. antiqu.).
A fine series in breeding plumage from May 7th to the end of the month,
on both islands.
"Common during the spring migration" (Stejneger, p. 132).
(Tringa gutlifer was not obtained. Stejneger mentions one specimen.)
57. Tringa erythropus (Pall.).
3 adults in fine black nuptial plumage from Bering Island, 23. v. 1913,
16. v. 1914, 18. v. 1914.
Rare spring migrant.
58. Tringa incana incana (Gm.).
11 fine adult males and females, Bering Island, 29. v to 12. vi, all in full
nuptial plumage.
Comes to the islands during the latter part of May, and may possibly breed,
Stejneger thinks.
59. Tringa incana brevipes (Vieill.).
cJ9, Bering Island, 25. v. 1914, 2.vi.l913.
9 in worn summer plumage, Bering Island, 24.x. 1911.
7 juv., both islands, 31 . viii to 1.x.
This is obviously the rarer form of incana, and Stejneger had obtained a
single specimen only. Buturlin, however, recorded a male shot in 1912. As
this is the Siberian form, which breeds in Kamtchatka, one would rather ex-
pect it to nest on the islands, than the American T. i. incana — probably neither
of the two does nest, though both pass through on migration.
60. Tringa glareola L.
17 specimens from the latter third of May and June, both islands, but only
a few from Copper Island.
Breeds, according to Stejneger, on Bering Island.
There are no subspecies of T. glareola..
61. Tringa hypoleuca L.
<J9, Bering Island, 22. v. 1912, 30. v. 1914, 29. v. 1913.
Rather rare migrant (Stejneger).
There is no eastern subspecies.
(" Terekia cinerea " recorded from one specimen by Stejneger.)
140 NOVITATES ZOOLOGICAE XXVII. 1920.
62. Philomachus pugnax (L.).
cJad., Bering Island, 18. v. 1911.
Evidently rare. Stejneger had only two specimens.
Ridgway rejects the name Philomachus because the author was anonymous.
This, however, is an arbitrary proceeding. It does not matter who described a
bird, or who created a genus, as long as this was formally done and the names
are acceptable under the Rules of Nomenclature. The names in the " Adum-
bratiuncula " to Vroey's catalogue were also published without an author's
name, and it was only found out incidentally that Pallas was the author. Leach's
name Pavoncella is unacceptable, as Leach's work was not published at the
time. Iredale called my attention to the fact that it was only printed as a list
of labels for the use of the British Museum's officials, that only one or two copies
exist, and that it was never for sale. The publication by the Willughby Society
was a rather unnecessary act, but at that time British ornithologists were more
reckless in the resurrection of forgotten old names than they are nowadays.
63. Numenius cyanopus Vieill.
$ ad., Copper Island, 14. vi. 1911.
A rare visitor.
64. Numenius phaeopus variegatus (Scop.).
8 <J<j> ad., both islands, 25. v to 26. vi. and 3 juv. 31 .viii to S.ix.
Stejneger secured only two specimens on Bering Island.
65. Phalaropus fulicarius (L.).
5 <J$, Bering Island, 25. v to 16.vi.
1 ad. Bering Island, 8 ad. and juv. Copper Island, September.
Stejneger only once observed a flock in autumn, but could not secure
specimens.
The late dates of Sokolnikoff's specimens suggest the possibility of breeding
on the island.
66. Phalaropus lobatus (L.).
4 ^ $ ad., Bering Island, May 26th and June 2nd to 26th. Also 6 September
birds from both islands.
Breeds numerously on Bering Island, teste Stejneger.
67. Megalornis canadensis canadensis (L.).
Ardea canadensis Linnaeus, Syst. Nat. i. p. 234 (1766 — " Habitat in America septentrionali." Ex
Edwards, pi. 133, restricted terra typica therefore : Hudson Bay).
cJ? ad., Bering Island, 18 and 20. v. 1914.
Has occurred several times in Tschuktschen Land and Anadyr, therefore the
occurrence on Bering Island is not very extraordinary. It probably visits the
island from time to time, as a long, long-legged, long-necked grey bird, according
to the natives, is observed occasionally (Stejneger, pp. 147, 135).
Novitates Zoolooicae XXVII. 1920. 141
68. Anser fabalis serrirostris Swinh.
Anser segetum var. serrirostris Swinhoe, Proc. Zool. Soc. London 1871, p. 417 (China, in winter near
Amoy).
Half a dozen adult males and females from Bering Island, May and June,
also a juvenile male, Bering Island, 9.x. 1911.
All the adult birds show very clearly the large, wide beaks with curved
under mandible of serrirostris, and even in the young one it is clearly indicated.
This again speaks very much for the distinctness of the two eastern forms,
serrirostris and sibiricus of Alpheraky, though their breeding- homes are not
properly known, and both together as well as intermediate specimens occur in
China on migration.
(Bianchi mentions both serrirostris and " mentalis," but the latter name is
a synonym of serrirostris ! )
69. Anser alburons (Scop.).
Two ? juv., Bering Island, 16 and 18. xi. 1911.
These appear to be typical albifrons. The so-called " A. albijrons gambelli "
cannot be upheld in the sense of certain ornithologists. American and East-
Asiatic White-fronted Geese are not as a rule larger or in any way different, but
it is true that extraordinarily large specimens occur in North America, though
their breeding range is unknown. It is therefore still possible that a large race
exists somewhere, but very doubtful. No North-east Asiatic example seen by
me is larger than some European ones. The conclusions of Swarth & Bryant,
Vnivers. California Publ. in Zool. xvii. no. 11, pp. 209-222, that both forms are
found in North America in winter quarters, are correct, but their supposed
differences do not exist. Neither is the number of rectrices constantly different,
nor the general colouration or size ; nor, as far as I can make out, the colour of
the eyelid ! Final judgment about the two forms cannot be passed, unless a
series from the various breeding-places be examined !
70. Anser caerulescens caerulescens (L.).
(Anser hyperboreus hyperboreus.)
A white female with partially brown secondaries and a few brownish feathers
on the mantle, Bering Island, 30. v. 1911.
If, as it seems to be the case, the grey-brown goose with blue-grey upper
wing-coverts and the white ones are one and the same (cf. among others Hesse,
Journ. f. Orn. 1915, pp. 159, 160, and Blaauw's breeding experiments !), the
species must be called caerulescens (Anas caerulescens Linnaeus, Syst. Nat., ed. x.
1, p. 124, 1758), and not hyperboreus (Pallas, Spicilegia Zool. fasc. vi. p. 25).
71. Branta canadensis hutchinsii (Rich.) (?).
$ ad., Bering Island, 22.vii.1914.
This specimen has 18 rectrices and a wing of a little over 400 mm. (400, but
worn!). American authors describe hutchinsii as having 14 to 16 rectrices,
" occidentalis " with 18 to 20 ; wings of the latter 41 1-458, while that of hutchinsii
appears to vary from 375 to 451 ! It seems to me that hutchinsii and occidentalis ,
are not separable !
142 NOVITATES ZOOLOGICAE XXVII. 1920.
72. Branta canadensis minima Ridgw.
<?? ad., Bering Island, 28. v. 1912.
These two specimens seem to be actual minima ! Rectrices 16 ! Wings
about 380 mm.
73. Branta bernicla nigricans (Lawr.).
$ juv., Bering Island, 9.x. 1910.
Stejneger (pp. 149, 135) also obtained only a single specimen, in November
1882.
74. Anser canagicus (Sewastianoff).
Adult males and females were obtained in October, November, January,
February, and April 14th, young of the year in December, all on Bering Island.
75. Cygnus cygnus (L.).
$% first winter plumage, 1 and 4 October, Bering Island.
Stejneger mentioned the species as observed but not positively identified,
but Bianchi seems to have received it.
(Stejneger obtained a young C . columbianus on Bering Island !)
76. Anas platyrhyncha platyrhyncha L.
(Anas boschas.)
c?e?$$, Bering Island, April and May.
1 (J ad., Copper Island, 28. iv. 1911.
There is quite a series from Bering, but only one male from Copper Island.
This seems to bear out what Stejneger wrote long ago : " Breeding numerously
in Bering Island, comparatively rare on Copper Island."
77. Anas strepera L.
The head of a $ shot on Copper Island on May 13th, 1911 is sent. It is
only a rare straggler, reported by Dybowski, but not observed by Stejneger.
78. Anas acuta acuta L.
May, July, and October, Copper and Bering Islands. Breeds numerously
on Bering, sparingly on Copper Island, teste Stejneger.
79. Anas crecca crecca L.
The teal breeds also on the islands, and was obtained by Sokolnikofi on
both, end of April, May and September.
80. Anas querquedula L.
Stejneger did not come across the Garganey, but Dybowski stated that it
had occurred on Bering Island. Sokolnikofi sent two adult males and a female,
obtained on Bering Island in summer.
N0VITATE3 ZOOLOQICAE XXVII. 1920. 143
81. Anas formosa Georgi.
£ ad., Bering Island, 16. v. 1911, 23. v. 1911.
cJ juv., Bering Island, 6.ix.l911.
? ad., Bering Island, 10. ix. 1911.
tj ad., Copper Island, 9.vi.l911.
Neither Stejneger nor Dybowski seem to have observed this species on the
Commander Islands, but Bianchi recorded it from Copper Island. From the
dates when birds were obtained it seems probable that it now breeds on the
islands, which is not strange, as it nests in Kamtchatka.
82. Anas falcata Georgi.
(Eunetta falcata.)
cJcJad., Bering Island, 17. iv. 1910, 17. v. 1914, 31. v. 1912.
^ ad., Copper Island, 14. v. 1911.
Stejneger says : " Occasionally straggling to Bering Island during the
spring migration."
83. Anas penelope L.
Obtained on both islands in May, on Copper Island as late as May 14th, 1911.
Stejneger says : " Visits the islands during the migration season."
(Anas americana Gm. was picked up dead — one specimen — by Stejneger
on Bering Island.)
84. Spatula clypeata (L.).
10 skins of both sexes, all collected on Bering Island from May 11th to
June 4th, 1915, one female, 11 .x. 1910. The June date suggests the possibility
of its nesting on the islands.
Stejneger calls it a summer visitor to Bering Island, and adds " possibly
breeding." Bianchi gives it as nesting.
85. Nyroca fuligula (L.).
Adult examples from both islands, from Bering Isle as late as 21.v, from
Copper even 5.vi, and one October specimen. The late dates suggest the
probability of breeding. Stejneger considered it rare, but admitted that it
" may breed occasionally."
85. Nyroca mania mariloides (Vig.).
Adult males and females from Bering and Copper Islands, shot in May and
June, one October.
Stejneger found the Scaup commonly breeding on Bering Island. He
considered the specimens to belong to N. marila marila, while he distinguished
N. marila marila : " Palaearctic Region."
N. marila nearctica (Stejn.) : " Nearctic Region."
N. affinis : " Nearctic Region."
N. affinis mariloides : " Pacific coast of Asia, from Japan southward."
144 NOVITATES ZOOLOGICAE XXVII. 1920.
I am sorry to say I cannot follow this arrangement. I find that all specimens
from the Far East — i.e. from Japan and China and from Bering Island — are (with
few exceptions) smaller than European N . m. marila, the wings of 1 6 adult male
examples measure 207-220 mm., in the European form 220-233 mm. Moreover,
in nearly all cases the black barring of the upperside is coarser, thus giving the
latter a darker appearance, which is particularly noticeable on the scapulars.
In many cases, but not always, the head and nape are more purplish, less greenish.
We must therefore, unless we suppress this form altogether, recognize a Far- East
form breeding on Bering Island, and probably in Kamtchatka, wintering in
China and Japan.
The North American form has been suppressed even by the splitting
American ornithologists, but I do not think that this is quite correct. I find that
American males have the back barred as in mariloides, or even darker, the scapu-
lars and wing-coverts very dark. Stejneger said, when describing them as
Nyroca (Aythya) marila nearctica (Bull. U.S. Nat. Mus., no. 29, p. 161, 1885),
that " the primaries from the fourth quill were without whitish on the inner
web." I cannot help thinking that he meant to say outer web, as I find no
differences on the inner web, while it is true that in most cases the outer webs
of the inner primaries are dark in American, with a white patch in European,
Scaups.
This, however, is not constant, as specimens without the white area occur
in Europe, others with white — though very rarely — in America. The size of
the American birds is as in N . m. marila, not as in N. m. mariloides. Under the
circumstances, we should, at least provisionally, distinguish between the following
forms :
Nyroca marila marila : Europe, N. Asia, but not known how far east replaced
by mariloides.
Nyroca marila mariloides : Bering Island, and probably Kamtchatka and
elsewhere. In winter China and Japan.
Nyroca marila nearctica : N. America.
Nyroca affinis : N. America.
It is undoubtedly quite wrong to treat N. m. mariloides as a subspecies of
affinis ! N . m. marila, mariloides, and nearctica are, in fact, very closely allied,
while affinis is as a rule quite distinct and inhabits similar areas to that of
nearctica. It must, however, be admitted that some specimens of affinis are not
so typical as most of them.
86. Nyroca ferina ferina (L.).
An adult male, Bering Island, 13. v. 1911.
This species is new to the islands and not known to extend so far eastwards.
Stejneger says : " Very doubtful. Not reported from Kamtchatka."
87. Bucephala clangula (L.).
$ ad. in full nuptial plumage, Copper Island, 30. iv. 1912 (wing, 228).
<J juv. (born in 1910), beginning to moult into adult plumage, Copper Island,
18. v. 1911 (wing, 211).
<J in very similar plumage, Copper Island, 11 .x. 191 1 (wing, 225).
NOVITATES ZOOLOGICAE XXVII. 1920. 145
2 $ ad., Bering Island, 6.x. 1911, 16. ii. 1914 (wings, 203, 212).
$ ad., Bering Island, 29. xi. 1911 (wing, 216 mm.).
$ ad., Bering Island, 1 . xii .1911 (wing, 197 mm.).
It seems to me that the females shot on Bering Island, 6.x. 1911, 16. ii. 1914,
and 29. xi. 1911, with wings of 203, 212, and 216 mm., must belong to the some-
what larger B. clangula americana (Bp.), while the other specimens are B. clangula
clangula (L.). From their plumage I do not think that the larger specimens can
be young males. The two subspecies are indistinguishable, except that in a
series the American race runs larger : wings, 228-240 (but seldom so large), while
European birds (adult males in both cases) have wings of 216-227 mm. As many
specimens overlap, single specimens are often indistinguishable.
Stejneger said of " Glaucionetta clangula " that it was " a not very common
winter visitor to the islands," but Sokolnikoff's specimens show that it also occurs
during the spring migration.
88. Bucephala albeola (L.).
cJ juv. (sexed " $," but must be a young male), Bering Island, 19. xi. 1911.
$, Bering Island, 13. i. 1911.
" An accidental visitor during the winter 1882-83 " (Stejneger).
89. Clangula hyemalis (L).
A series of winter birds, Bering Island, November to April, and one young
male, Copper Island, 31.x. 1910.
According to Stejneger one of the commonest ducks on Bering Island, where
it is resident throughout the year and breeds numerously. Yet Sokolnikoff has
not sent any specimens in summer plumage, nor young in down ! The wings of
adult males measure from 224-235 mm., while sometimes eastern specimens are
larger, wing up to 240, but by no means constantly.
90. Histrionicus histrionicus pacificus Brooks.
Histrionicus histrionicus pacificus Brooks, Bull. Mus. Comp. Zool. Harvard College, lis. p. 393 (1915 —
North Pacific Ocean. Type Kamtchatka).
Fully plumaged adult males, Bering Island, 12.xi. 1910 to end of December ;
two males in eclipse, Copper Island, 15.viii. 1911 ; young male quite like females,
but larger, Copper Island, 9.x. 1910 ; males moulting into first winter garb from
both islands, December and January ; two females, Bering and Copper Islands,
October and December.
Stejneger says it occurs round the islands all the year round, " but apparently
without breeding."
Differs from H. h. histrionicus only in the larger bill. The chestnut-red
stripe on the sides of the crown is not always paler and no character at all to
distinguish the two races.
91. Polysticta stelleri (Pall.).
A number of both sexes throughout the winter. The earliest specimen is
a specimen from Copper Island, September 5th, and there is one from October.
The latest is a female from Bering Island, 9. v. 1913.
10
146 NOV1TATES ZOOLOOICAE XXVII. 1920.
According to Stejneger, on the shores of the islands in winter in countless
numbers, arriving at the beginning of November and staying until after the
middle of May.
92. Somateria mollissima v-nigrum Gray.
<J $ ad., Copper Island, 15 and 18. vi. 1911.
" Breed in very limited number in a few places on Copper Island, only
occasionally flying over to Bering Island, round the shores of which it may be seen
in winter " (Stejneger).
93. Somateria spectabilis (L.).
$, Bering Island, 4. i. 1912.
Rare winter visitor.
94. Oidemia fusca stejnegeri Ridgw.
2 d'ad., Bering Island, 24. iv. 1913, 3. v. 1912.
3 o1 juv., moulting into the black plumage, Bering Island, 17 and 12. v. 1912,
and Copper Island, 23. iv. 1911.
6 $, both islands, October, November, and May.
Stejneger says : " Rare in autumn and spring."
96. Oidemia fusca deglandi Bp.
2 adult males, Copper Island, 14. iv. 1911, and Bering Island, 24. v. 1912,
and a female, Bering Island, 10. xi. 1913, are not 0. f. stejnegeri but deglandi.
One of the males has the underside black, but the sides of the body brown in
clear contrast, while the other has the whole underside brown, from the jugulum
backwards. Both have the knob above the nostrils much less high than usual
in stejnegeri and convex, not concave, in front ; neither of them have the black
line in front of the knob, which is obvious in males of stejnegeri. The female has
the frontal feathers continued along the culmen right over the commencement
of the nostrils, a character which I have not seen in a female of stejnegeri, and
which seems to be peculiar to those of deglandi.
Brooks (Bull. Mus. Comp. Zool. Harvard Coll. lix. p. 393, 1915) described
Oidemia fusca dixoni from Arctic Alaska, said to have the bill shorter in comparison
to its length and wider, blunter at the tip. I am afraid I cannot appreciate these
supposed differences, which seem to me to be individual, not racial, otherwise
the Commander Islands specimens should more likely belong to the Alaskan
subspecies.
97. Oidemia perspicillata (L.).
<J ad., Bering Island, 3.vi.l912.
cJ juv., Bering Island, 6.xi.l911.
The young male has a triangular patch on the hindneck, formed by white
tips to the feathers.
This species had not been observed on the Commander Islands by Stejneger,
but Bianchi records it from Bering Island ; as, according to Palmen, it nests
in the Tschuktschen Peninsula, the occurrence is not strange.
Noyitates Zoolooioae XXVII. 1920. 147
98. Oidemia nigra americana Swains.
In winter on both islands, adult male as late as 18. iv. 1913, and a young
male, beginning to moult into the black garb, even May 18th, 1912.
99. Mergus merganser merganser L.
cj ad., Bering Island, 1. v. 1913, 13. v. 1911.
cJ ad., apparently already in eclipse, Bering Island, 13. v. 1911.
<J juv., Bering Island, lO.xii. 1910.
$, Bering Island, 2.vi.l912.
One male has a rather distinct black alar bar, but not as wide as in M . m.
americanus. The difference in the feathering on the bill is so very little different
from that of M . m. merganser, that not much value can be attached to that !
100. Mergus serrator L.
Adult males in full winter plumage were shot on both islands from May 15th
to June 5th, a young male on Copper Isle, 10. ix. 1910, a female on 9.x. 1910.
Evidently both M. merganser and serrator breed on Bering Island. Two young
in down were sent, but whether they belong to serrator or merganser is doubtful.
101. Mergus squamatus Gould.
A male was shot at Copper Island, 9 . vi . 1 91 1 .
This is a very interesting specimen, evidently a juvenile male apparently
in partial eclipse plumage, the hind-neck and back being mixed with obviously
fresh ashy grey feathers, while the blackish feathers on these parts are more or
less old — though a few black feathers are also growing ! The upper head and
neck are covered with brown, worn feathers, while deep black-green ones are
putting in an appearance. I thus presume that this bird, though juvenile, and
moulting the brown neck into the black-green of the adult, is assuming a
partial eclipse garb on the back, which had already become black.
Moreover, the locality of this specimen is of the greatest interest. While
hitherto this species was only known from China, where La Touche collected
specimens in winter and Zappey, among others, a series in Sechuan in November
and December, Buturlin recorded an adult male on August 13th on the Lower
Amur, and now Sokolnikofi got it in June on Copper Island ! We must there-
fore suppose that M. squamatus nests in East Siberia and winters in China,
chiefly Sechuan, Fokien (La Touche), and Hunan.
102. Mergus albellus L.
This species does not breed on the islands. An adult male in full plumage,
Bering Island, 7. v. 1911 ; $ ad., Copper Island, 9. v. 1911 ; (J juv., Bering Isle,
3.x. 1911.
103. Phalacrocorax pelagicus pelagicus Pall.
This species, which, notwithstanding the enormous mortality by apparently
an epidemic disease in 1876-77, is very numerous on both islands, was collected
in autumn, winter, May and June
148 Novitates Zoolooicae XXVII. 1920.
104. Phalacrocorax urile (Gm.).
Only three juvenile birds were obtained on Bering Island. This species
is much rarer and more difficult to shoot than P. p. pelagicus, according to
Stejneger. The name urile of 1789 is based solely on Pennant's " Red-faced
Cormorant," it must therefore be adopted instead of that of Ph. bicristatus, which
is used in the Cat. B. Brit. Mus.
105. Phalacrocorax perspicillatus Pall.
Now extinct. (Cf. Stejneger and Taczanowski.)
Sokolnikoff collected some sterna. Though very much persecuted for
food and said to have been much more stupid than other species, I fancy that
not the persecution by men alone, but an epidemic like the one of 1876-77 (when
perspicillatus is said to have been already extinct !) settled its fate.
106. Lagopus mutus ridgwayi Stejn.
Lagopus ridgwayi Stejneger, Proc. Biol. Soc. Washington, i. p. 98 (1884 — Bering Island) ; id. Om-
Erpl. Commander Islands and Kamtschatka (Bull. 29, U.S. Nat. Mus.), p. 194.
Lagopus rupestris Gm. subsp. insularis Bogdanow, Consp. Av. Imp. Ross. i. p. 34 (1884 — Bering
Island).
A very fine series in full winter and summer plumage, juv. and pull., mostly
from Bering Island.
This subspecies has the <J in nuptial plumage darker, more rufous, somewhat
of the colour of a Red Grouse, the pullus is brighter, more yellowish. Wings of
adult males 195-201, ? 185-197 mm.
107. Falco rusticolus candicans Gm.
Falco candicans Gmelin, Sysi. Nat. i. 1. p. 275 (1788 — Terra typica substituta, Hartert, Vog. pal.
Fauna, p. 1064 : Greenland !).
Falco rusticolus uralensis Sewertzoff & Menzbier, Menzbier's Orn. Geogr. Europ. Russl. p. 228. pi. iii.
(1882 — Ural Mountains. Russian !).
Hierofalco Grebnitzkii Sewertzoff, Nouv. M6m. Soc. Imp. Nat. Moscou, xv. livr. 3. p. 69. plate (1885 —
Bering Island).
4 white juv., 4 dark young, 1 white ad., 3 dark adults from both islands
(mostly Bering), all shot in the winter months.
These birds are indistinguishable from Greenland specimens. It is true that
5 of these 12 show the 4th primary as long as the 1st, but (though I did not find
this character in 50 Iceland and Greenland ones) it occurs also in Greenland,
from where I have examined two with the 4th primary as long as the 1st ; in
3 Tobolsk ones it is also obvious, in a fourth, however, not at all. I can, therefore,
no longer accept uralensis and grebnitzkii, and consider F. r. candicans to be a
circumpolar form, inhabiting Greenland and the arctic regions of America to
Baffin- Land, northern Siberia to the Commander Islands. It is represented by
two somewhat disputable southern subspecies, F. r. obsoletus in Labrador, and
F. r. islandus in Iceland (cf. Vog. d. pal. Fauna, pp. 1064-1068), and a well
separable one in Scandinavia, the true Falco rusticolus rusticolus, which of
course never occurs in North America, though American ornithologists, not
NOVITATES ZOOLOQICAE XXVII. 1920. 149
having grasped the fact that these birds in the arctic regions occur in dark and
white varieties, admit it as a " species."
Two of the dark-backed young birds show fresh grey-barred feathers, proving
again that they moult into the dark adult variety only, while white birds remain
white.
Stejneger did not separate the white Bering Island Falcons from candicans,
and distinctly said already that the alleged plastic differences of the so-called
grebnitzkii were of no value whatever. He found a few pairs of the white Falcon
breeding on Bering Island, and he believed that the dark birds were only winter
visitors.
108. Falco peregrinus pealei Ridgw.
cj ad., Bering Island, 29. iv. 1913.
12 (J $ juv., Bering and Copper Islands, September to January.
? juv. of last year (1913), Bering Island, 4. vi. 1914.
<J juv., evidently just flown, Copper Island, 29. vi. 1911.
The old bird, apparently nesting on the island, agrees well with descriptions
and a male from Vulcan Island (cf. Vog. pal. Fauna, p. 1049). The 14 young
birds are remarkably constant, all being very dark on the underside, and the
upperside having no rusty buff edges to the feathers or only very narrow ones,
so that they look quite black from a distance.
Nesting on both islands, breeding on high and inaccessible cliffs, according
to Stejneger (p. 206).
109. Falco peregrinus calidus Lath.
4 cJ$ juv., Bering Island, October 1910 and 1913.
Easily distinguishable from the young of F. p. pealei. The upperside is less
black and has wide pale rust-coloured edges to the feathers ; there is more white
on the sides of the head, and the underside is much more white and buff. The
feathers of the breast and abdomen may be described as buff with a dark brown
shaft-stripe, those of the young of F. p. pealei as black-brown with pale buff
edges, and sometimes similar roundish spots — which are also present on the
browner flanks of F. p. pealei.
110. Falco columbarius insignis (Clark).
[Falco coluinliarius Linnaeus, Syst. Nat. ed. x. i. p. 90 (1758 — " America ").]
Aesalon regulus insignis Clark, Proc. U.S. Nat. Mus. xxxii. p. 470 (1907 — Fusan, Corea).
$>, Bering Island, 10. vi. 1915.
Not hitherto recorded.
111. Buteo lagopus pallidus (Menzb.).
4 (J$ ad., Bering Island, 15. v. to 8.vi.
These birds are very typical pallidus. The upperside shows much more
white than European specimens, sharply contrasted with brown, but without
any grey. Also the underside is not cream-colour but white, with the usual
brown markings, as a rule, more restricted. Wings, (J 43-5-44-5, "§" (?)
only 42-5 mm.
150 Novitates Zoolooicae XXYII. 1920.
112. Haliaeetus pelagicus (Pall.).
cJ jun., approaching adult dress, Bering Island, 18.iii.
Only an occasional visitor, according to Stejneger.
(" H. hypoleucus" still mentioned as a species in Bianchi's list, is a variety
of H. albicilla. Neither the latter nor leucocephalos was obtained by Sokolnikofi . )
113. Pandion haliaetus haliaetus (L.).
c? ad., Bering Island, 28.vii.1913.
$ ad., Copper Island, 23. vi. 1913.
These specimens have only an indicated brown breast band, like P. h.
carolinensis, but similar specimens occur in Europe. The short wings (about
460, but worn, and 470 mm.) prove them to belong to the European — Asiatic
form. Stejneger quotes this Osprey as an occasional visitor to Bering Island
only. He obtained specimens on Kamtchatka only.
114. Nyctea nyctea (L.).
cJ ad., Bering Island, 31 . vii . 1914.
Upperside white, with the exception of a few small spots on scapulars and
primaries, and a few bars on the secondaries ; in moult, growing secondaries
with black bar.
$ ad., Bering Island, 6. v. 1912.
Above and below with brown-black bars.
12 cJ$, Bering Island, September 2nd to April 2nd, but mostly December
and January, varying from the darkest form with broad blackish bars to white
with a few scattered spots and bars.
It is a popular idea that these (and other) birds become whiter with age,
but there is apparently no foundation for it.
(No specimen of Asio jlammeus (Pontopp.) (accipitrinus auct.) was sent by
Sokolnikoff, though Stejneger found it resident on both islands.)
115. Aegolius funereus magnus (But.).
[Striz funerea Linn., Syst. Nat. i. 1. p. 93 (1758—" Habitat in Europa").]
Nyctala magna Buturlin, Orn. Monatsber. 1907. p. 80 (" Kamtschatka und das Gebiet von Kolymsk ").
cj ad., Bering Island, 31. i. 1911.
I suppose this must be Ae. f. magnus, of which I saw the type twelve
years ago, but I have no specimens of either magnus or jakutorum, if the latter is
different. The Bering Island specimen has more white on the upperside and is
larger than Ae. f. funereus. Its wings measure 179 to 180 mm.
The species is new to the islands.
116. Cnculus canorus telephonus Heine.
c? ad., Bering Island, 25. vi. 1914. Wing 221.
$ ad., Bering Island, 19. vi. 1915. Wing 204 only.
Novitates Zoolooicae XXVII. 1920. 151
$ ad., Bering Island, 26. v. 1914. Wing 207 only.
" <5 " (?)» apparently a last year's bird, Bering Island, 11 .vi. 1915.
The females are of the usual grey colour.
117. Cuculus optatus Gould.
cJ ad., Copper Island, 5.vi.l911.
9 ad., Bering Island, 15.vi.1912. Grey variety.
$ ad., Bering Island, September. Red-barred variety.
In C. optatus the latter is very common.
118. Dryobates major kamtschaticus (Dyb.).
(Stejneger rejected the name kamtschaticus because of the former existence
of a " kamtscJtatkensis " ; both names are, however, easily distinguished and
cannot be considered to be synonyms. Stejneger' s " purus" is therefore a
synonym of kamtschaticus. In practice both names are also widely different,
the one being a subspecies of major, the other of minor ! )
cJcJ ad., Bering Island, 17. v. 1913 and 17.x. 1912 ; $ ad., 19.x. 1912.
These are very typical ; wings 134, 140, and 135-5 mm. Two of these are
smaller than those measured when I wrote my account in Vog. pal. Fauna,
p. 907.
D. m. tscherskii (p. 908) is exceedingly close to kamtschaticus, only the
wings are generally (not always) shorter, and the bills less powerful and often
shorter. The lateral tail-feathers of tscherskii have also, as a rule, more black
than in kamtschaticus, but sometimes appear not to be different in this respect.
Woodpeckers are, of course, only occasional visitors on Bering Island, where
there are no forests, so that it cannot be a real Woodpecker home.
119. Alauda arvensis pekinensis Swinh.
Alauda pekinensis Swinhoe, Proc. Zool. Soc. London 1863, p. 09 (Peking).
Alauda blakistoni Stejneger 1884, 1892.
c??$, Bering Island, 9. v. 1912, 29. v. 1913.
According to Stejneger, " apparently a regular summer visitor to Bering
Island, where a few pairs probably breed."
120. Anthus gustavi Swinh.
Anthus gustavi Swinhoe, Proc. Zool. Soc. London, 1863, p. 90 (Amoy).
Anthus stejnegeri Ridgway, Proc. U.S. Nat. Mus. 1883, p. 95 (Bering Island).
6 cj$ ad., both islands, all shot in June.
A common breeder on the islands, not arriving before the end of May
(Stejneger).
121. Anthus cervinus (Pall.).
3 <J? ad., Bering Island, 20. v. 1913, 29. v. 1912, 29. v. 1913.
Stejneger did not come across the Red-throated Pipit and knew only of one
occurrence. Anthus anadyrensis Allen 1905 is a synonym of cervinus.
152 NOVITATES ZOOLOGICAE XX VII. IV2U.
122. Anthus spinoletta japonicus Temm. & Schleg.
Anlhus pratensis japonicus Temminck & Schlegel, Siebold's Fauna Japon., Aves, p. 59. pi. 24 (1847 —
Japan).
cj ad., Bering Island, 13. v. 1911.
? ad., Bering Island, 31. v. 191 4.
? ad., Copper Island, 15. v. 1911.
According to Stejneger, not observed on the islands.
123. Anthus (trivialis) macula tus Jerd.
Anthus vwcalatus Jerdon, B. India, iii. p. 873 (1864 — India. Ex Hodgson, nomen nudum !).
cjad., Bering Island, 27. v. 1913.
c? ad., Copper Island, 18. v. 1911.
Also new to the islands.
124. Motacilla flava simillima Hart.
Motacilla flava leucostrialus Stejneger, nee Homeyer !
Motacilla flava simillima Hartert, Vog. pal. Fauna, p. 289 (1905 — Breeding Kamtchatka. Type
Sulu Islands).
8 £ ad., Bering Island, lo.v to 9.vi.
1 (J ad., Copper Island, 16. v.
This form is of particular interest, because it so closely resembles M. flava
flava of northern Europe, though nearly the whole of Siberia is inhabited by
M. /. thunbergi and the Baikal and Amur districts by M, f. taivana. In fact,
one cannot say that simillima differs constantly in colour at all from flava, though
generally the yellow underside is perhaps paler, and this has to be confirmed
by specimens in fresh plumage. The only other differences are a somewhat
larger bill and foot, especially larger hind-claw. The length of the wing is supposed
to be greater, but the Commander Islands specimens do not bear this out ;
their wings measure from 77-5 (worn, perhaps really 78) to 85-6 (worn, perhaps
really 86) mm. The jugulum is, as a rule, much spotted with dusky, but this
occurs also in other forms, and is, therefore, not much of a distinguishing character.
125. Motacilla cinerea melanope Pall.
[Motacilla cinerea Tunstall, Orn. Brit. p. 2 (1771 — Name for the " Grey Water Wagtail " of the
Zoologia Britannica and the " Hoche-queue ou Bergeronette jaune " of Brisson).]
Motacilla Melanope Pallas, Reise Russ. Reichs. iii. p. 696 (1776 — Dauria).
3 <$ ad., Bering Island, 28. v. 1911, 29. v. 1912, 30. v. 1914.
2 ? ad., Copper Island, 6. v. 1911, 4.x. 1910.
" One of the rarer spring migration visitors to Bering Island " (Stejneger),
126. Motacilla alba ocularis Swinh.
5 adults, Bering Island, 9 . v to 1 . vii.
"?" ad., Copper Island, 31. v. 1911.
Probably a more or less regular spring visitor to the islands. Stejneger
obtained a single specimen.
NOVITATES ZOOLOGICAE XXVII. 1920. 153
127. Motacilla alba lugens Kittl.
6 adults, Bering Island, 26. iv. to 16 .vi, and two September specimens.
According to Stejneger, a regular spring migration visitor only, which does
not remain to breed.
128. Muscicapa (Siphia) parva albicilla Pall.
cj ad., Copper Island, 7.vi.l911.
$ ad., Bering Island, 5.vi.l914.
The male has more red on the throat than usual, there is even a red patch
on the chest.
129. Muscicapa griseisticta (Swinh.).
Butalis pollens Stejneger (p. 144) is doubtless a synonym. The species is
only a very exceptional visitor to the islands. Stejneger had one single example.
Sokolnikofl sent 1 " <j> " in worn plumage and dirty, obtained on Bering
Island 5.vi.l912.
Parrot described a Muscicapa griseisticta habereri from Iturup, Kurile Islands,
because it had — a single specimen ! — a wing of 90 mm. That is indeed an
exceptional measurement, but our Bering Island bird has a wing of fully 88 !
It is of course possible that a larger form exists, but that could only be proved
by a series from its nesting-place.
(No specimen of Muscicapa sibirica is in the collection of which Stejneger
said it was " exceedingly numerous." Probably that is the case in certain years,
but not always.)
130. Bombycilla garrulus (L.).
c? ad., Bering Island, 16. v. 1911.
$ ad., Copper Island, 21. v. 1911.
A rare visitor. Stejneger mentions only two specimens.
131. Troglodytes troglodytes pallescens (Ridgw.).
cj ad., Bering Island, 5.x. 1911.
1 (J ad., 1 juv., Copper Island, 18.x., 19. viii. 1911.
Resident on both islands, but commoner on Copper Island, according to
Stejneger.
132. Locustella ochotensis (Midd.).
Acrocephalus ochotensis apud Stejneger.
c?$ ad., Copper Island, 12, 14. vi. 1911.
$ ad., Bering Island, 2.vii.l913.
c$ juv., Bering Island, 2.x. 1911.
The young bird has the underside yellowish, and evidently no white tips to
tbe rectrices, though very dirty.
154 Novitates Zoolooicae XXVII. 1920.
133. Phylloscopus borealis borealis (Bias.).
2 ad., Bering and Copper Islands, 6.vi.l914, 16.x. 1911.
Visits the islands regularly in spring, and Stejneger thinks it is possible that
some may remain to breed. (The treeless islands seem to me a most unlikely
place for a Phylloscopus to nest.)
134. Turdus fuscatus Pall.
Turdus /meatus Pallas, Zoogr. Rosso-Asiat. i. p. 451 (1827 — Dauria).
9 ad., Bering Island, 20. v. 1911.
cJ ad., Copper Island, 19. v. 1911.
Stejneger quoted the occurrence of a single specimen, under the name of
Turdus eunomus.
135. Turdus obscurus Gm.
J$ ad., Bering Island, 26, 27. v. 1914.
cJ ad., Copper Island, 18. v. 1911.
" Visits Bering Island occasionally during the spring migration " (Stejneger)>
136. Tarsiger cyanurus (Pall.).
6 (J? ad., Bering Island, 28. v to 4.vi.l912, 1914, 1916.
9 ad., Copper Island, 31. v. 1911.
Stejneger obtained a single straggler, 21. v. 1883.
137. Luscinia calliope (Pall.).
5 cJ $, Bering Island. 27 . v. to 1 6 . vi .
3 c?> Copper Island, 3.vi. to 21. vi.
Sokolnikoff evidently found these "occasional visitors" more numerous
than Stejneger, and probably they pass over the islands fairly regularly in spring.
138. Oenanthe oenanthe oenanthe (L.).
Motacilla Oenanthe Linnaeus, Syst. Nat. ed. x. i. p. 1S6 (1758— Europa, terra typica : Sweden).
9 juv., Bering Island, 23. ix. 1915.
cJ juv., Copper Island, 2.ix.l912.
Not in Stejneger's and Bianchi's lists. Apparently a rare passage migrant.
139. Riparia riparia ijimae (Lonnb.).
Clivicola riparia ijimae Lonnberg, Journ. Coll. Science Tokyo, xxiii. art. 14. p. 38 ( 1908 — Sachalin) ;
Hartert, Vog. pal. Fauna, p. 813.
1 ad., sex doubtful, Copper Island, 20. vi. 1911.
Bianchi had it from Bering and Buturlin from Copper Island.
(Hirundo rustica tytleri is an occasional straggler, but was not obtained by
Sokolnikoff.)
Novitates Zoolooioae XXVII. 1920. 166
140. Emberiza aureola Pall.
2 cJ, 1 ?, Bering Island, 2, 4.vi.l914.
Occasional visitor during spring migration, according to Stejneger.
141. Emberiza rustica Pall.
1 cj, 2 ?, Bering Island, 12. v to 27. v.
2 J, 2 9, Copper Island, 16. v to 21 .v.
Occasional visitor during spring migration, according to Stejneger.
(Emberiza variabilis Temm. & Schleg. has occasionally occurred, but we did
not receive specimens.)
142. Calcarius lapponicus coloratus Ridgw.
Calcarius lapponicus coloratus Ridgway, Auk, xv. p. 320 (1898 — Type: Copper Island).
2 r? ad., 2 $ ad., 1 juv. in first plumage, Copper Island, May and June, the
young bird 16. v. 1911.
1 (J ad., 2 $ ad., Copper Island, May and June.
The date of the young bird, just out of nest, is, if correct, very early.
Stejneger did not notice the species earlier than April 21st, and found eggs from
May 23rd to June 11th. The commonest breeding bird on both islands.
C. I. coloratus differs from C . I. lapponicus in being larger, bill larger, wings
longer, 95-5-104-5 mm., and the secondaries and upper wing-coverty of the
males have wider rust-brown edges ; the $ has the neck-band, as a rule, more
marked and less thickly spotted.
143. Plectrophenax nivalis townsendi Ridgw.
Plectrophenax nivalis townsendi Ridgway, Manual N. Amer. B. p. 403 (" Prybilof Islands, Alaska,
and Commander Islands, Kamtschatka." Type : Otter Island in the Pribilof group).
6 <J, 5 $, autumn, winter, May and June, both islands. Wings, <J 115-5 (once),
117-118, 120 (once), $ 112-112-5 mm.
According to Ridgway (B. North and Middle Amer. i. p. 152), a male from
Bering Island measures 120, but according to Stejneger (p. 250), others measured
only 110 and 113, though I doubt this is strictly correct. If adult males with
unworn ivings have wing-measurements of 110 and 113, they are not bigger than
European P. n. nivalis, while 120 is unknown in western specimens. Ridgway
says that birds from "Aleutian Islands, including Commander Islands," Pribilof
and Shumagin Islands have larger dimensions, " with relatively longer bill."
Now this is perfectly true with regard to the Commander Islands birds, which
have larger bills and longer wings ; but the Pribilof and Aleutian examples have
not longer wings, specimens in the British Museum (measured by Thomas Wells)
having wings of (^ ad.) 105, 111, 116 mm.
Possibly the Commander Islands birds will have to be separated again from
the Pribilof and Aleutian ones. Ridgway measures an adult male from Plover
Bay, Siberia, with a wing of 113-3 mm., and says that " the largest specimens
are those from the more western Aleutian Islands, including the Commander
Islands, Kamtchatka ; the smallest are from Unalashka and the Shumagin
Islands, at the opposite end of the chain. These latter are in reality intermediate
156 XOVITATES ZOOLOGICAE XXVTI. 1920.
between the island form and true P. nivalis, but seem nearer the former and,
therefore, best referred to it."' He then gives " average " measurements, but
unfortunately no individual ones, except where only one is measured. Average
measurements are, in my opinion, misleading unless taken from a large series.
144. Carduelis linaria linaria (L.).
14 r?$, both islands, 1 January, 3 May, 1 June, 1 July 8th, 4 October. 1
November, the rest with doubtful dates, apparently labels interchanged.
There is a good deal of variation in this series, both in the bills and in the
length of wings, but not one of these specimens has a bill as large as the specimen
of holboelli. The wings do not exceed 78. except in one specimen with a very
small bill and a wing of 79, while most of them have wings of 75 to 70, females
less in most cases.
Stejneger did not think that this form was breeding on the islands, as he
did not come across it between the end of May and November. Sokolnikofl,
however, sent 1 June and 1 July bird.
145. Carduelis linaria holboelli (Brehm).
A <$, Bering Island, 18. v. 1914, has a wing of 82-0 mm. and a strikingly
higher and longer bill than all the above linaria, 12-5 mm. long. Stejneger
obtained specimens of this form as late as June 13th, and says that it breeds
on the islands. Sokolnikoff also sent a male, said to have been shot Bering
Island 22. vi. 1912, but its plumage is too fresh for that date, and I consider it
to be an autumn bird. This bird has a bill larger than what I consider typical
linaria, i.e. nearly 12 mm. long, but the wing only 78 mm. Is it a hybrid or
what?
There is still some doubt about " holboelli.'' Is it a subspecies, a species
or individual variety ? It nests together with C. I. linaria in its northern habitats
but — I believe — not in its southern area. Is there any country where it alone
nests ?
(No form of C. hornemannii has been sent by Sokolnikoff, but Stejneger
obtained seven specimens of C. hornem. exilipes in winter, between November
and March.)
146. Montifringilla tephrocohs maxima (Brooks).
Leucosticte griseonucha maxima Brooks, Bull. Mils. Comp. Harvard Coll. lix. p. 405 (1915 — Type :
Copper Island).
18 cj$ ad., from various winter and spring months, both islands ; 1 juv.,
Copper Island, 15. ix. 1911.
Wings, <$ 1 18-123, $ 113-119 mm. The pink spots on the upper tail-coverts
are, as a rule, less bright in the females, otherwise the sexes do not differ in
coloration.
Resident on the islands. Larger than the Unalashka form, M. t. griseonuclta.
Adult specimens from St. Paul, Kodiak, and St. George's Islands in the British
Museum (measured by Thomas Wells) have wings of 109-114, twice 121 mm.,
while Ridgway gives average measurements of 1 12-78-1 17-80 and 119-13-121-92
for the Commander birds.
NOVTTATES ZOOLOOICAE XXVII. 1920. 157
147. Fringilla montifringilla L.
5 cj, 2$ ad., Bering and Copper Islands, 1 4. v to 24. v.
<J ad. (wrongly sexed $ !), Bering Island, 8.x. 1913.
Regular visitor, but not nesting, according to Stejneger.
It seems to me impossible to recognize an eastern subspecies (F. m. sub-
cuneolata Kleinschm.). There is the same variation in the outer tail-feathers,
the same extent of white. Sometimes specimens are very dark brown, but others
are not, and also in Europe similarly dark brown individuals occur.
148. Carpodacus erythrinus erythrinus (Pall.).
£ (red), Copper Island, 11 . vi. 1911.
cj (brown), Copper Island, 8.vi.l911 ; Bering Island, 2.vi.l914.
$ ad., Bering Island, 5.vi.l913.
I cannot distinguish these birds from C. e. erythrinus of Russia and the
Baltic Provinces, and East Prussia. I cannot help doubting the difference of
C. e. grebnitskii Stejn., from Kamtchatka, which is said to have a brighter red
male.
The species was unknown to Stejneger and Bianchi as occurring on the
islands, where it is probably only a straggler.
149. Pinicola enucleator kamtschatkensis (Dyb).
Corythus enucleator kamtschatkensis Dybowski, Bull. Soc. Zool. France, viii. p. 367 (1883).
A female, unfortunately with left leg and attached label wanting, but probably
from Bering or Copper Island. Differs from females of P. e. enucleator in being
paler throughout, the back without orange-yellow, almost pure grey ; bill thicker.
This species had not been obtained before.
(A Crossbill — " Loxia curvirostra," according to Bianchi — has occurred on
Bering Island, but we did not receive specimens.)
150. Coccothraustes coccothraustes japonicus T. & S.
Coccothraustes vulgaris japonicus Temminok & Schlegel, Siebold's Fauna Japan., Aves, pi. 51 (1850 —
Japan).
S ad., Bering Island, 24. v. 1912.
New to the islands.
151. Pyrrhula pyrrhula kamtschatica Tacz.
Pyrrhula kamtschatica Taczanowski, Bull. Soc. Zool. France, 1882, p. 395 (Kamtchatka).
tj ad., Bering Island, 27. vi. 1914.
$ ad., Copper Island, 1 .vii. 1913.
This rare Kamtchatkan Bullfinch had not previously been obtained on the
islands.
The <J has the upperside of a clearer grey than P. p. pyrrhula, the outer
tail-feather has always a white wedge on the outer web. The female has the
back less brownish and the underside lighter brownish.
158 Novitates Zoolooicae XXVII. 1920.
(Parus atricapillus kamtschatkemis is supposed to have been seen by a Cossack
on Bering Island, but has not been obtained. Cf. Stejneger.)
(" Corvus corone levaillanti " is mentioned by Stejneger as a rare straggler.
These birds can, of course, not be levaillanti — a tropical form — but must be
C. c. orientalis, which is found in Kamtchatka.)
152. Corvus corax subsp.
There is a remarkable series of not less than 20 Ravens from both islands,
from January, February, April, June (1 juv.), July, September, October, and
November (11).
At present I am unable to say with absolute certainty to which race these
Ravens belong. Their wings measure 405 ($ ad.) to very nearly 445 mm. Their
wings are thus not longer, on an average even a little shorter, than those of
European C. c. corax, but the feet and tarsi are very much stronger, heavier, and
the bill larger, wider. One specimen from Anadyr appears to be indistinguishable.
Two specimens (said to be males) from Yesso have the bills narrower, not so
powerful, also the feet a little less strong than the males from the Commander
Islands.
In the Vog. d. pal. Fauna, pp. 4, 5 (1903), I kept doubtfully separate C. c.
sibiricus, ussurianus, kamtschaticus, and behringianus, merely stating the differ-
ences as given by Taczanowski and Dybowski.
Buturlin (Mess. Orn. 1915, p. 107, 114, Russian with short English extract)
united kamtschaticus, ussurianus, and sibiricus, and so did Poljakov (t.c. p. 17).
They correctly stated that all Siberian Ravens have the first primary shorter
than the seventh, and it seems that Taczanowski's contradictory statements
were not correct, or based on exceptional varieties.
Buturlin, however, had apparently no Ravens from the Commander Islands,
and Sokolnikoff paid, by special instructions from St. Petersburg, special attention
to Ravens, and brought together the present series, that it should be compared
with Siberian and Kamtchatkan Ravens. Unfortunately, I am not able to do
this, but I have been promised Kamtchatkan Ravens, and when they arrive,
will go into the question again. Either the Bering and Copper Island Ravens
are sibiricus or they form a separate subspecies : behringianus.
Novhates Zooloqicae XXVII. 1920. 159
NOTES ON AND DESCRIPTIONS OF SPHINGIDAE.
By Dr. Karl Jordan.
(With six text- figs.)
1. Polyptychus paupercula senniger subsp. nov. (text-fig. 1).
<J. A P. p. paupercula Holl. ( 1 889), armatura genitali distinguendus : harpa
leviter trilobata.
Hab. Bingerville, Ivory Coast, June, August, and September — October,
1915, 4 <J<J (Gaston Melou), type ; Takwa, Gold Coast, 1 <$ (R. E. James).
There are no differences in colour and pattern between the specimens from
the districts Senegal — Niger and Niger — Congo. All 5 (J<J we have from the
former district, though differing slightly inter se in the shape of the harpe, are
distinguished from the more southern subspecies in the apical margin of the
harpe being bisinuate ; the lower sinus is narrow and fairly deep, while the
upper sinus is shallow (text-fig. 1).
2. Polyptychus molitor R. & J. (1912) (text^figs. 2, 3).
We described this species from some $$ in the collection of the British
Museum obtained by H. A. Foy at Ibi on the River Benue, Nigeria ; cf . Novitates
Zoologicae, xix. p. 132, no. 4 (1912). The Tring Museum has since received
2 ^cj and 1 § from Sedhiou, Senegal, collected by R. Castell, the <J(J being caught
in October 1917 and the $ dated simply 1917.
The (J is smaller than the $ ; the forewing is narrower, its distal margin
more oblique; with the apex more produced. Antenna stouter than in $, seriated
cilia longer, otherwise similar to that of the $. Palpi larger than in the $, joint
closed, third segment small in both sexes (not two-thirds of second as stated in
the original description), second segment a little longer than wide measured to
the base of the third (i.e. exclusive of the apical scaling).
Tenth tergite (text-fig. 2) very hairy, broad, divided by a rounded sinus
into two sharply pointed processes ; tenth sternite represented by a low mem-
branous ridge. Clasper without friction-scales, deeply concave on the inner
side, the ventral margin elevate ; above this ridge, in the cavity, a second ridge,
the two ridges uniting distally and forming a large, pointed, conical process
placed about halfway between dorsal and ventral margins and being almost vertical
upon the plane of the clasper, leaning a little proximad (text-fig. 3). Apical
portion of clasper weakly chitinised, nearly membraneous, clothed with long
scales. Penis-funnel cylindrical, longer than broad ; penis-sheath also cylindrical,
slightly widened at the apex, without armature.
3. Polyptychus orthographus R. & J. (1903).
We have now a specimen of the ?, from Luluaburg, Kassai, Congo. It
agrees in markings with the J, but is much darker both above and beneath.
The distal margin of the forewing is convex, with the apex projecting, the marginal
area being wider than in the <J. The antenna bears prolonged seriated cilia, but
the lateral grooves are indistinct, and the segments have a straight ventral
outline (lateral aspect).
160
Novitates Zoolooicae XXVII. 1920.
4. Polyptychus reussi Strand (1911).
Our statement in Novitates Zoologicae, xxiii. p. 260, no. 23 (1916), that
in Strand's description the costal margin of the forewing below is said to be
Flo. \.~Polyptychu/i paupercula eenniger, $ ; harpe.
Flo. 2. — Polyptychus molitor, <$ ; anal tergite.
Fig. 3. — Polyptychus molitor, $ ; clasper.
dark red is erroneous. I misread the description, which agrees with the $ of
P. coryndoni R. & J. (1903). Strand's name, therefore, is a synonym.
5. Temnora nitida spec. nov. (text-figs. 4, 5, 6).
<$. Cervina ; alis anticis fascia olivacea fere recta oblique a costa ad
marginem exteriorem extensa extus luteo marginata ornatis atque lineis trans-
NOVITATES Z00LOGICAE XXVII. 1920.
161
versis e lunulis olivaceis compositis signatis ; posticis aurantiaco-rufis, fascia
marginali brunnescente. Infra rufo-avellina, lineis e lunulis et angulis parvis
compositis olivaceis notata.
Long. al. ant. 26 mm., lat. 11 '5 mm.
Hob. Diego Suarez, N.E. Madagascar, December 1916 (G. Melou) ; 3 $$.
In the bright rufous hindwing this new Temnora resembles T. elegans Roths.
(1894), but the oblique band of the forewing distinguishes nitida at once from
that species.
Body fawn-colour, abdomen more rufescent ; the scales on the thorax above
Fig. 4. — Temnora nitida, $ ; anal segment, lateral view.
Fig. 5. — Temnora nitida, $ ; harpe.
Fig. 6. — Temnora nitida, £ ; penis-sheath.
and beneath and on the upperside of the head pale-tipped ; underside rufescent,
somewhat paler than upper. An ill-defined line above eye, another on second
palpal segment likewise diffuse and inconspicuous, and scales at joint between
first and second palpal segment creamy ; abdomen beneath with two rows of
olive-black dots ; foretibia externally deep fawn-colour.
Wings, above. Forewing fawn-colour, outer margin evenly rounded-convex
in middle, concave anteriorly and posteriorly, not crenulate ; a well-defined
olive band runs from the middle of the costal margin to below middle of outer
margin, about T5 mm. broad anteriorly, widening digitally and here shading off
to anal angle, on the distal side the band bounded by a pale line, which varies
11
162 Novitates Zoolooicae XXVII. 1920.
in distinctness ; in basal half two pairs of transverse excurved lines, olivaceous,
somewhat scalloped and more or less interrupted at the veins, the proximal
pair rather indistinct, the second pair about 7'5 mm. from base at costa and
ij mm. at hindmargin ; on disc a third pair, crenulate, extending from costa
beyond band to hindmargin 1 1 mm. from base, excurved anteriorly and somewhat
incurved posteriorly, i.e. slightly S-shaped ; further distally another pair, more
or less indistinct ; the costal portions of the discal lines form a darkish triangular
patch distally to the band, the base of the patch at the costa being about as long
as the distance from the apex of the wing ; below apex a marginal luniform
pale olive spot bounded proximally by purplish fawn scaling ; such scaling,
which is slightly glossy, is found all over the forewing excepting the dark markings
and the subapical, sepia-brown, area. Hindwing orange-rufous ; a darker,
hazel, marginal band about 2"5 mm. wide below apex at its widest point, not
strongly contrasting, bearing small black dashes on the veins, before anal angle
a fawn-coloured diffuse patch.
Underside duller than upper, rufous-hazel, forewing cinnamon-rufous from
base to beyond middle ; outer half of both wings with four transverse lines,
blackish above, dentate or crenulate, varying in distinctness, accentuated on the
veins ; below tip of forewing a blackish marginal cloud ; abdominal area of
hindwing paler than rest of wing.
Genitalia : both the tenth tergite and sternite long and slender (text-fig. 4),
the former with the tip convex and entire ; the sternite more acuminate with the
apex dentate on the upperside. Clasper with five large friction-scales. Harpe
(text-fig. 5) lying flat on the surface of the clasper, tapering, with the apex slightly
turned upwards. Sheath of ejaculatory duct with an elongate patch of teeth
ending apically with a small hook ; a swelling along the side of the patch
continues proximad half around the sheath (text-fig. 6).
6. Some Individual varieties of Xylophanes turbata Edw. (1887).
A series of 1 ^ and 8 $$ of this species from Orange Walk, British Honduras,
caught in May and June 1917, recalls the Eastern Hippotion velox F. (1793) by
the variation in the pattern of the forewing. Two of the $$ are normal, having
a conspicuous double line extending from the apex of the wing to the basal third
of the hindwing, and five thin and inconspicuous lines between the double line
and the outer margin, of which the mostMistal one is barely indicated. In the
(J and one $ of the above series the double line is represented by a single thin
line (corresponding to the outer line of the pair) and the following line is scarcely
traceable. In the remaining 5 $$ the double line has more or less completely
disappeared, excepting a dash at the wing-apex, which the other lines join. The
brown cloud distally to the apex of the cell is distinct in all the specimens.
Novitates Zoolooioae XXVII. 1920. 163
THE STATUS OF PLATYSPHINX BOURKEI TRIMEN (1910).
By De. Karl Jordan.
r T^HE four species of Hawkmoths which we united in the new genus Platysphinx
J- in the Revision of the Sphingidae (1903) are very similar to each other in
colour and pattern. Therefore, when Dr. Trimen sent us a coloured sketch of
a specimen very unlike those four species, we agreed with him that the sketch
represented a new species, which Trimen then described as PI. bourkei, in Ent.
Mo. Mag. (2), xxi. p. 209 (1910) (Zululand).
In 1918 we received an example of this PI. bourkei, together with some
specimens of what appeared to be Platysphinx jriabilis Distant (1897), all bred
by E. E. Piatt at Eshowe, Zululand. Mr. Piatt, in a letter to us, pointed out
that bourkei and piabilis were obtained from apparently identical larvae, and
as, moreover, some of the imagines were somewhat intermediate, he asked us to
investigate the structure of bourkei in order to ascertain whether bourkei was
different from piabilis apart from colour. We compared the specimens early
in 1919, and the result was as expected by Mr. Piatt. PI. bourkei agrees with
piabilis in structure. Considering the great colour-similarity of the other species
and their equally great dissimilarity in structure, that result was rather startling,
and induced us to study all the material of Platysphinx we now have in the
collection.
1. Platysphinx constrigilis.
When writing the Revision we had only a $ from Sierra Leone and a much-
damaged <$ from the " Niger Coast Protectorate." Our series consists now of
19 $<$ and 2 $$. There is a good deal of individual variability in the detail of
the colouring and pattern, but all specimens agree in the hindwing beneath and
the costal area of the forewing above and below being more or less suffused with
white in between the transverse markings, and in the forewing having a strongly
crenate submarginal line on both surfaces.
The tenth tergite of the <J is broad, with the lateral margin uneven, the apex
bent down, narrowed and truncate-emarginate. The tenth sternite is geo-
graphically and individually variable, being long and either spiniform or more or
less club-shaped. The clasper has at the base a long spiniform process projecting
distad. This process, which lies on the ventral side of the ventral margin of
the clasper and well separated from that margin, also varies geographically.
The penis-funnel has a small conical projection on each side (not a ventral process
as stated in the Revision, our figure on plate xxx of that work giving a lateral,
not a ventral, view), and the apex of the large penis-sheath is produced downward
into a pointed process, which is concave on the upperside and resembles the
spout of a jug. This process is much more curved in some specimens than in
others.
In the $ the vaginal aperture is flanked on each side by a pointed process
curved mesad.
We cannot find any reliable distinctions in colour and pattern between the
164 NOVITATES ZOOLOQICAE XXVII. 1920.
two geographical races into which the species has developed, as evidenced by
the structure of the genitalia.
a. PI. constrigilis vicaria subsp. nov.
Platysphinx constrigilis R. & J., Revis. Sphingidae, p. 224. no. 185. tab. xvii. fig. 3, xxiv. fig. 9,
xxx. fig. 23, xxxiii. fig. 1 (1903) (partim. ; Sierra Leone and Niger Coast Protectorate, nee
Cameroons and Congo).
(J. Tenth abdominal sternite slender, slightly or not at all dilated before
apex ; ventral spiniform process of clasper long, slender, straight or very little
curved inward in ventral aspect.
$. Process at side of vaginal orifice broad at base, almost gradually narrowed
to near apex, here its outer margin rounded, apex pointed and directed mesad,
the tip slightly twisted and therefore appearing, under a low power, rather
shorter than it is in reality.
Hab. Sierra Leone, type, 1 <$ (Bainbridge) and 1 $ (Clements) ; Wassaw
district 45 miles, Akjah-bippo 46 miles, and Prestea 75 miles inland from
Sekondi, Gold Coast, 5 cj^ ; Bibianaha, 70 miles north-west of Dimkwa, 700 ft.,
7. xi. 1910 (Spurrell), 1 ^ ; Obouassi, Gold Coast, September and November
1909, 2 $3 ; Bingerville, Ivory Coast, March and April 1915 (Melou), 2 <$c5 ;
Nigeria and 'L Niger Coast Protectorate," 2 cJcJ.
b. PI. constrigilis constrigilis Walk. (1S69).
Originally described from the Congo.
cJ. Tenth abdominal sternite strongly widened-rounded before apex ;
ventral process of clasper less slender than in the north-western subspecies, curved
inward in a ventral view.
$. Process at side of vaginal aperture slenderer than in the previous case,
more gradually narrowing, the apical half particularly narrower.
Hab. Niger to Congo. In the Tring Museum from : Ilesha, Nigeria
(Humfrey), 1 <J ; Cross R., Nigeria (Martell), 1 (J ; Bopoto, Upper Congo (Kenred
Smith), 3 cJcJ, 1 $ ; Upper Congo, 1 J.
It would be of interest to know whether the two subspecies occur anywhere
near one another in Nigeria.
The remaining specimens of Platysphinx in our collection (and in that of
the British Museum) represent three modifications of one type. The three forms
strictly replace each other geographically according to the specimens inspected
and differ constantly in the structure of the tail-ends only. The form designated
by us in the Revision as PI. ■phyllis is found from the Senegal to the Niger ; the
second, sligmalica Mab. (1878), inhabits the countries from the Niger to the
Congo basin; and the third, piabilis Dist. (1897), is known to us from the countries
further to the south-east : Rhodesia, South Nyasaland, Portuguese East Africa,
and Zululand. The distribution given in the Revision must be corrected
accordingly.
The South-Eastern insect is, in structure, the most strongly modified of
the three. The antenna of the <J are rather longer and stouter, and the distal
margin of the forewing is somewhat less incurved posteriorly than in the West
Novitatks Zoolooicae XXVII. 1920. 165
African forms. I consider the differences to indicate that piabilis has attained
to that degree of physiological aversion towards the allied forms which we now
consider a true criterion of specific distinctness.
The West African forms are more similar to one another. We have only
one <J among the North- Western specimens, and this c? agrees in structure much
more closely with the Niger-Congo <$<$ than is the case in the ??, while piabilis-g
is very different in the tail-end. For that reason I am inclined to regard the
two West Coast forms as geographical races of one species. But there is just a
possibility that our North- Western <J is not the true c? of phyllis ; I should like
to compare a second (J from the North- Western district before altering the status
of phyllis and stigmatica we have assigned to them in the Eevision.
2. Platysphinx phyllis R. & J. (1903).
There is, apparently, no difference in colour and pattern between this and
the following species. The type-specimen of phyllis is a $ with comparatively
few spots on the hindwing ; the four examples we have received since 1903 do
not share this peculiarity.
<$. The tenth abdominal tergite broader than in the next subspecies, the
apical sinus wider, and the apical process of the clasper much shorter.
$. Vaginal plate posteriorly to orifice on each side with a finger-like curved
process.
Hab. Senegal to Niger. In the Tring Museum from : Sedhiou, Casamance,
(native collector), 1 $ ; Konakry Island, Sierra Leone, 1 ?, type ; Wassaw
district, 45 miles inland from Sekondi, Gold Coast, 1 <? ; Sekondi, Gold Coast
(Hamlyn), 1 $ -; Zunguru, Nigeria, 1 $.
3. Platysphinx stigmatica Mab. (1878).
We have specimens only from the Congo and Angola. The species, how-
ever, occurs doubtless also northward to the Niger. The specimen recorded in
the Revision from Portuguese East Africa belongs to PI. piabilis.
Hab. (Niger to) Northern Angola. In the Tring Museum : Bopoto, Upper
Congo (Kenred Smith ; Oram), 5 <$<$, 1 $ ; south of Congo (Bentley), 1 ? ;
Dondo, Northern Angola (v. Homeyer).
4. Platysphinx piabilis Dist. (1897).
Platysphinx stigmatica R. & J., Revis. Sphing. p. 225. no. 186 (1903) (partim ; Port. E. Afr.).
Platysphinx bourkei Trimen, Ent. Mo. Mag. (2). xxi. p. 209 (1910) (Etshowe, Zululand).
The $<$ from Rhodesia southward agree with the type from the Transvaal
in the distinctive structure of the tail-end, as illustrated in the Revision, pi. xxiv.
fig. 10, xxx. fig. 22, xxxiii. fig. 2. The specimen of bourkei received from Mr.
Piatt shows the same structure. This is convincing evidence that bourkei is a
colour-aberration of piabilis, if we consider the structural differences found in
the other forms of this genus. However, it is a most interesting aberration,
which I am inclined to look upon as the ancestral colour-type of Platysphinx.
The sexual armature of the $ recalls that PI. stigmatica-^. The walls of the
aperture are produced as a cylinder, more or less regular, with a deep sinus on
166 NOVITATES ZOOLOGICAE XXVII. 1920.
the anterior side ; this cylinder is not supported as in stigmatica by a lateral
wing, and the postvaginal plate is much less chitinised and smaller than in that
species.
The specimen labelled Portuguese East Africa and received from Messrs.
Staudinger and Bang-Haas is larger than the others and has a deeper sinus to
the genital cylinder. An East African subspecies ?
Hab. Rhodesia to Zululand. In the Tring Museum from : Solwezi,
Rhodesia (Dollman), 2 ?$ ; Ruo Valley, South Nyasa (Neave), 1 <J, 1 ? ; Portu-
guese East Africa, 1 ? ; Eshowe, Zululand (Piatt), 1 <J, 1 $ and 1 $ ab. bourkei.
Novitates Zoolooicae XXVII. 1920. 167
SOME NEW AFRICAN SPHINGIDAE.
By Dr. Karl Jordan.
(With two text-figs.)
rpHE specimens described in this paper are all in the collection of A. J. T.
-L Janse, of Pretoria, who kindly sent them to us for study and description.
1. Polyptychus molitor Iautus subsp. nov.
$. Magnus, colore cremoris lutescentis, thorace linea mediana et ala antica
quatuor lineis transversis olivaeeo-fulvis, alis tenuissime ochraceo marginatis,
linea tertia alae anticae lata.
Al. ant. long. 59 mm., lat. 26 mm.
Hab. Barberton, Transvaal (L. de Beer) ; 1 $.
A very large form. Entirely cream-colour slightly washed with buff, much
paler than P. m. molitor, which is more or less pinkish buff. Upperside of
tibiae and tarsi ochraceous, foretibia and first foretarsal segment with a
chocolate stripe on outer side. Middle line of thorax and four lines on fore-
wing olivaceous tawny, the lines placed as in P. m. molitor R. & J. (1912) from
the north-west of tropical Africa, but the inner line of the discal pair much
broader and shading off outwardly ; hindmargin edged with orange- buff except
base ; from apex to vein M2 a large marginal drab area, half-moon-shaped,
sharply defined at apex of wing, elsewhere diffuse, nearly reaching outer line,
the veins in this patch remaining pale except towards distal margin.
Hindwing rather paler than forewing, especially at base, with vestiges of two
darker lines, of which the inner one touches the cell.
On underside : the ground-colour nearly as above, palest towards base ;
forewing with a slight diffuse yellowish tint around lower cell-angle ; both wings
crossed in outer half by two nearly parallel brown lines, of which the inner one
is slightly the broader and, on the hindwing. is about 1 mm. distant from the
lower cell-angle ; as in P. in. molitor the forewing beneath has no dark marginal
area ; the inner line on both wings costally less curved than in the N.W. African
race.
2. Libyoclanis metria spec. nov. (text-fig. 7).
cJ. L. vicinae affinis ; alis anticis sine linea apicali obliqua, apice non
productis ; posticis rufis margine abdominali pallide luteo ; segmento anali
ventrali bilobato.
Al. ant. long. 36 mm., lat. 12-5 mm.
Hab. Emangeni, Rhodesia, 18. i. 1918 (A. J. T. Janse) ; 1 <J.
The upperside of the head, thorax, and base of abdomen cinnamon with a
tint of isabella colour, rest of abdomen creamy buff, breast pale clay colour.
Upperside of femora and underside of tibiae creamy buff washed with pink ;
tibiae and tarsi olive-gray, the tibiae pinkish towards apex.
Wings, upperside. Forewing pale clay-colour ; apex pointed but not
168
NOVITATES ZOOLOGICAE XXVII. 1920.
produced, the distal margin not incurved below apex, more evenly convex than
in L. vicina R. & J. (1915) ; the basal tuft of hindmargin more or less pink
proximally and cinnamon distally ; between base of wing and vein Ms a few
blackish scattered scales which indicate a transverse line proximally to base of
M2 ; about halfway between cell and distal margin a transverse line faintly
curved in S-shape, commencing at costal margin 9 mm. from apex and crossing
M2 4 mm. from distal margin, the four posterior internervular sections of the
line more or less luniform ; on the proximal side of this line faint indications of
another line parallel to the former ; a fuscous patch extends from hind angle to
beyond R!, bounded by the discal line, occupying the whole space between line
and fringe from hind-
margin to M1, then nar-
rowing ; 5 mm. from apex
between SC4 and SCB an
ill-defined fuscous spot
composed of black dis-
persed scales; cilia
ochraceou s-buf f.
Hindwing carmine-pink,
costal margin paler, ex-
treme base and the abdo-
minal edge whitish cream,
abdominal marginal
border cream- buff, widen-
ing considerably at anal
angle, and extending
along distal margin but
soon fading away, distal
margin dusted with black
scales ; wing shaped as
in L. vicina, but distal
margin a little less in-
curved.
Underside of the
colour of the abdo-
men. Forewing with
the cell (except base) and the area behind cell carmine-pink, this colour ex-
tending to hindangle and distally fading away ; the outer discal line anteriorly
quite distinct, posteriorly barely indicated, not reaching hindmargin, proximally
to a faint blackish bar behind point of bifurcation SC'1'5 ; marginal area
rather worn, without trace of the straight line which in the allied species runs
from the apex obliquely to the disc. Hindwing with a few black scales in
the outer half, these scales more numerous at and near the costal margin,
forming a minute, ill-defined costal spot 5 mm. from apex.
Antenna as in L. vicina, but slightly thicker. Anal tergite also as in that
species, except that the two lobes are slightly shorter. Anal sternite different,
being divided into two rounded lobes (text^fig. 7). Penis-funnel without dorsal
lip, ventral lip carinate below. Above the funnel on each side a rounded lobe
about as large as the lobes of the anal sternite, with scalloped edges, each tooth
3*
' ;■■'.■ •//;
■ ><:
Fig. 7. — Libyoclanis metria, <$ ; anal sternite.
Fig. 8. — Xenosphingia jansei, q ; head from below.
NOVITATES ZOOLOGICAE XXVII. 1920. 169
denticulate and bearing a hair on the ventral side ; the corresponding lobes of
L. vicina small, with the teeth vestigial. Harpe as in L. vicina, but slightly
broader at the apex.
Xenosphingia gen. nov.
Generi Ceridia R. & J. (1903) dicto affinis ; antennis fortissime pectinatis,
palporum articulo tertio longissimo tcnui subcylindrico ad latus versus proiecto ;
rostro nullo ; tibiis anticis et mediis spinosis, antica brevi, sine calcareo, postica
duobus calcareis apicalibus armata.
Genotypus : X. jansei spec. nov.
A very strange genus, which shares with Ceridia the long-pectinated antenna,
reduced foretibia, aborted proboscis, etc., but differs remarkably in the absence
of the foretibial spur and in the length of the third segment of the labial palpus.
Antenna (<3) reaching beyond apex of cell of forewing. bipectinate from base
to tip, the branches of the central segments 15 mm. long, all scaled to the apex,
shaft setiform in dorsal aspect, ventrally each segment dilated into a slightly
claviform process which projects downward and is longer than a segment, with
the exception of the processes of the proximal segments, of which the processes
are short.
Palpus : first segment short, rough with long hair-scales ; second long,
flattened laterally, and here as well as at apex smooth-scaled, apex curved side-
ways ; third as long as second, smooth, slender, rod-like, nearly cylindrical,
directed laterad ; joint between first and second open ventrally (text-fig. 8).
Abdomen without spines.
Foretibia about one-third shorter than first tarsal segment, broad, without
epiphysis, spinose on upperside, four apical spines long, the two central ones of
them the longest. Midtibia spinose, a little longer than the first tarsal segment.
Hindtibia without spines, half as long again as the first hindtarsal segment, with
one pair of spurs, longer spur twice as long as the tibia is broad before apex.
All the tibiae and tarsi smooth. Pulvillus and paronychium present, the latter
with one fringed lobe on each side.
Wings entire ; frenulum and retinaculum present. Forewing : SC2 nearer
to SC1 than to apex of cell ; stalk of subcostal fork short. Hindwing : SC2 and
Rl together from upper angle of cell, D1 distinctly curved, not quite twice the
length of D' = D1, lower cell-angle about 90°, not produced.
3. Xenosphingia jansei spec. nov. (text-fig. 8).
cJ. Viridis, antennis albis ramis anticis purpureo-squamosis, pedibus ex
parte purpureis, alis anticis margine costali albato, posticis pallidioribus.
Al. ant. long. 18 mm., lat. 9 mm.
Hab. Sawmills, Rhodesia, 2. ii. 1918 (A. J. T. Janse) ; 1 <J.
Upperside of body and forewing a soft chromium-green. Shaft of antenna
and branches of posterior ( = outer) side creamy white, anterior branches purple,
underside of both shaft and branches ochreous. Palpi and forecoxae washed
with purplish tawny ; upperside of forefemur, a lateral stripe on mid- and hind-
tibiae, the whole foretibia and tarsus, and the upperside of the mid- and hindtarsi
purple.
Wings, above. Forewing : costal edge creamy, shaded with fuscous
170 Novitates Zoolooicae XXVII. 1920.
in outer third, cilia of hindmargin, a posterior basal tuft, the longer scales of
the fringes and a minute stigma creamy white ; parallel with distal margin and
about 3 mm. distant from it a faint darker green line ; apex acuminate but not
produced, distal margin straight below apex, then convex, hindangle rounded,
projecting neither backward nor outward. Hindwing : paler than forewing,
whitish green, base and hair of abdominal margin almost white ; distal margin
as in forewing even, neither dentate nor undulate, anal angle faintly indicated.
Underside pale green, costal edge of forewing creamy buff ; longest scales
of fringes and the abdominal area of the hindwing whitish.
Novitates Zoologicae XXVII. 1920. 171
THE BIRDS OF BUCKINGHAMSHIRE AND THE TRING
RESERVOIRS.
By ERNST HARTERT axd FRANCIS C. R. JOURDAIN.
(Plates XII, XIII.)
BUCKINGHAMSHIRE, being a purely inland county, is naturally less rich
in records of migrating species than many others with extensive coast
lines. It is therefore not surprising that comparatively few of the rarer and more
accidental visitors have been recorded, but, on the other hand, it compares favour-
ably with other inland counties. It has the advantage of varied scenery, for, with
the exception of the south-east corner, most of the county north of the Thames
valley is decidedly hilly, especially along the main ridge of the Chiltern Hills,
which, however, lies for the most part within the Oxfordshire boundary, and
attains in places a height of over 800 ft. Both the Chiltern slopes and the Chiltern
Hundreds may be described as more or less dry chalk hills, wooded in places,
chiefly with beech, and bare and open in other parts. Perhaps the two most
interesting ornithological features of this district are the presence of the Cirl-
Bunting, which is not rare near Wendover and Tring, and does not range much
farther north in England, and the Stone-Curlew, which was formerly common,
and still preserves a precarious existence in spite of agricultural operations which
often result in the destruction of its eggs. The north of the county is to a great
extent composed of grass land, with here and there beautifully- wooded parks,
watered by little streams ; while the group of large reservoirs in the Tring district
naturally attracts all the aquatic species in the district, and has a special interest
as being the first definitely known breeding-place of the Black-necked Grebe in
England for over forty years. Though lying chiefly in Hertfordshire, they touch
the border-line of Bucks, while the Halton Reservoir is entirely within our county
boundary. It is therefore impossible to exclude them from a survey of the Birds
of Buckinghamshire.
The Tring Reservoirs are now four in number. Three of these (Marsworth,
Startop's End, and Tringford or Little Tring) form a group with a water-
area of about 87 acres ; while the fourth and largest, Wilstone Reservoir,
formerly divided into three, covers no less than 120 acres. In dry seasons the
water-surface is much diminished, and the great expanse of mud and sand then
exposed proves a great attraction to the Waders. Unfortunately at the beginning
of the present century, when the water-level was low, Mr. Oldham had not begun
to make regular observations in the district, and Hartert's time was too fully
occupied to allow of much field work, while of late years the water has been con-
tinuously high and the number of visiting Waders has been in consequence much
restricted.
We must not omit to mention the presence of the one great river which forms
our southern limit, shut in by high ground on the west, and opening out lower
down more and more widely till the great level from Eton to Staines and West „
Drayton is reached, mucli of which is only 50 or 60 feet above sea-level. This
172 NOVTTATES ZOOLOOICAE XXVU. 1920.
part of the county has quite a character of its own, and differs widely from the
swelling uplands crowned with woods of the north of the county.
Although, as will be seen from the Bibliography, a good many scattered notes
on Birds have appeared from time to time, only two attempts have been made up
to the present to compile an account of the Birds of the County.
In 1S68, Alexander W. M. Clark Kennedy, then, as he describes himself "an
Eton Boy," published a neat little volume of 232 pages on The Birds of Berkshire
and Buckinghamshire. Considering that the author was only sixteen years of age
at the time, the book is a most praiseworthy effort. After so promising a begin-
ning to an ornithological career, one might well have expected that the author
would achieve great distinction in this branch of science with more matured
experience, yet with the exception of a few letters and short notes published in the
Ibis, Zoologist and Field, this was his first and last work on birds. Retiring from
the army, he led a country life at Knockgray, and died at the early age of forty-
two in 1894.
In 1902 the senior author of this treatise compiled, with the help of the
present Lord (then the Hon. Walter) Rothschild, a list of the Birds of the County,
which appeared in 1905 in the first volume of the Victoria History of the County of
Buckingham. In this work 208 species were enumerated, and the principal sources
of information were Clark Kennedy's book referred to above, notes in an old
manuscript preserved at Dinton Hall, the records relating to the Tring Reservoirs
published in the Transactions of the Hertfordshire Natural History Society, informa-
tion kindly supplied by the Rev. H. D. Astley (formerly resident at Chequers
Court), Mr. A. Heneage Cocks, Mr. Alan F. Crossman, Mr. Heatley Noble, Mr.
Charles J. Wilson, and others, as well as personal observations in many parts
of the county.
Many, in fact most, of the records of birds from the Tring Reservoirs men-
tioned in this work are confirmed by the presence of the specimens in question in
the Tring Museum. The present Lord Rothschild has shot over the Reservoirs
for thirty-five years past, and Hartert with him since 1892, while the keeper, James
Street, has a good knowledge of birds and is always on the look-out for rare visi-
tors. Unfortunately the list of Birds occurring at the Tring Reservoirs by the
then Hon. W. Rothschild, published in the Transactions of the Hertfordshire Natural
History Society, v. pp. 70-84, was not actually compiled from the specimens in the
Museum, but was written from memory. At that time few of the birds obtained
were labelled with exact localities and dates, and some errors were therefore
unavoidable. Moreover, some specimens were accidentally burnt by the care-
taker prior to 1892, so that in one or two cases the evidence is not conclusive.
For the last twelve years Mr. Charles Oldham has visited the Reservoirs
practically every Sunday, and has placed his valuable observations at our dis-
posal. We must also acknowledge the help received from Mr. Oliver Pike, who
resided for some time near Marsworth Reservoir, and took many excellent photo-
graphs of bird-life there. The old manuscript at Dinton Hall, in which many of
the birds obtained in that neighbourhood are well figured in water-colours and
described, was commenced by Sir John van Hatten in 1772, and the observations
were continued by the Rev. W. Goodall into the beginning of the nineteenth
century. Both Lord Rothschild and Dr. Hartert have examined this interesting
MS. and verified the accuracy of the quotations, which were made by Sir John
van Hatten's great-grandson, the late Colonel Goodall, who died a few years ago.
NOVITATES ZOOLOOICAE XXVII. 1920. 173
In addition to the Tring Museum, there is also a local collection of birds in the
Bucks County Museum at Aylesbury, which contains some specimens of great
interest. This collection has been visited by Hartert on several occasions, and
the curator, Mr. Edwin Hollis, has also kindly supplied us with valuable details.
There is also a collection of mounted birds in the Museum of Eton College,
bequeathed to the College by the late Dr. Thackeray, Provost of King's College,
Cambridge. According to the Guide to the Museum of Eton College of 1899, p. 1
(appendix), this collection contains mostly specimens from Berks, and Bucks.,
including some hitherto unrecorded ones, and those marked (u) are from Bucks,
only. Unfortunately this is not correct. Mr. W. D. Hill kindly informs us that
the specimens in question have no exact localities and dates, and that nothing is
known about their history. They are, therefore, probably the species mentioned
in Kennedy's book, but not necessarily obtained in Berks, or Bucks. Thus the
Great Black Woodpecker, Scops-Owl, Stilt, Bed-footed Falcon, Gadwall, Night-Heron,
and White Stork mentioned in the Guide cannot be taken as records of occurrences
in Bucks.
In supplying notes from the southern part of the county, and more especially
from the Thames Valle}', we have had the assistance of Mr. E. E. Pettitt, who has
made a special study of the bird-life of the river. Mr. A. Heneage Cocks has also
kindly furnished a series of ornithological extracts from his diaries, and Mr. W. D.
Mackenzie contributes some interesting notes from the Fawley district. The
Bibliography was originally compiled for the Geographical Bibliography of British
Ornithology, by Messrs. W. H. Mullens, H. Kirke Swann, and the Rev. F. C. R.
Jourdain, where it was published in a somewhat condensed form in 1919. It is
mainly the work of the last-named writer, who desires to thank his collaborators
for permission to reproduce this section with fuller references and some addi-
tional matter, including records relating to the Tring Reservoirs. Finally, we
must acknowledge our great indebtedness to Lord Rothschild for much assist-
ance freely rendered, and for the great interest he has taken in the work.
The numbers in brackets are those of the Hand-list of British Birds, 1912.
1 (1). RAVEN. Corvus corax corax L.
B. of Berks, and Bucks, p. 39. Vict. Hist of Bucks, vol. i. p. 138.
Now rare straggler, formerly resident.
We have only a few notes on the occurrence of the Raven in Buckinghamshire,
but it was probably a regular breeding species in olden times. In the manuscript
at Dinton Hall are figures and notes of Ravens shot on March 25, 1828, and
December 16, 1829. In 1868 Clark Kennedy wrote (p. 39) that " a few pairs
have bred in Windsor Park from time immemorial," and Windsor Park is close
to the borders of Bucks. Mr. Grossman (in litt.) states that on August 14, 188 7,
he saw one of these birds at Farnham, near Slough, which he distinctly recognized
by its hoarse note.
2 (2). HOODED CROW. Corvus comix cornix L.
B. of Berks, and Bucks, p. 112. Vict. Hist, of Bucks, vol. i. p. 138.
Winter visitor.
Generally more or less scarce, but sometimes occurs in fair numbers. (
Although seldom met within the hilly districts, it becomes more common along
174 Novitates Zoolooicae XXVII. 1920.
the Thames Valley and on the plains near Cheddington, Mentmore, and Leighton
Buzzard. Locally known as " Royston Crow." A male shot near Aylesbury,
February 25, 1907, is in the County Museum.
3 (3). CARRION-CROW. Corvus corone corone L.
B. of Berks, and Bucks, p. 39, Vict. Hist, of Bucks, vol. i. p. 138.
Resident generally.
Although greatly reduced in numbers in those districts where much game
preservation is carried on, this species manages to maintain a precarious existence
almost everywhere. Where game is scarce and the birds are not shot when
nesting, it is not uncommon, and is one of the species which have shown a
perceptible increase since the war.
C. M. Prior (Zool. 1876, p. 5005), writing from Old Wolverton, mentions a
case where after four eggs had been taken from a Crow's nest, a second laying
of four eggs was discovered in the same nest twelve days later. He adds that
three birds were always to be seen in company at the nest.
4 (4). ROOK. Corvus frugilegus frugilegus L.
B. of Berks, and Bucks, p. 40. Vict. Hist, of Bucks, vol. i. p. 138.
Very numerous resident.
There is hardly a park in the county without a rookery ; some are even
placed in gardens in the middle of towns and villages.
5 (5). JACKDAW. Coloeus monedula spermologus (Vieill.).
B. of Berks, and Bucks, p. 40. Vict. Hist, of Bucks, vol. i. p. 138.
Numerous resident.
In spite of much persecution by keepers, common in many places, especially
where there is much old timber. Nesting in hollow trees, old buildings, chimneys,
and Rooks' nests.
6 (6). MAGPIE. Pica pica pica (L.).
B. of Berks, and Bucks, p. 42. Vict. Hist, of Bucks, vol. i. p. 138.
Resident.
Generally distributed, but everywhere more or less scarce, on account of
the strict game- preservation during the past decades. Apparently increased
since 1914.
7 (8). SLENDER-BILLED NUTCRACKER. Nucifraga caryocatactes macrorhynchus
Brehm.
Once recorded,.
A specimen was killed near Whitchurch, October 7, 1911, and is now in the
County Museum at Aylesbury (Edwin Hollis, in litt., also examined by E.
Hartert. The specimen was received in the flesh).
Novitates Zoolooicae XXVII. 1920.
175
8 (10). BRITISH JAY. Garrulus glandarius rufitergum Hart.
B. of Berks, and Bucks, p. 42. Vict. Hist, of Bucks, vol. i. p. 138.
Common resident.
More or less common in all wooded districts. This species has increased in
numbers considerably since 1914.
9 (9). CONTINENTAL JAY. Garrulus glandarius glandarius (L.).
Rare winter visitor.
There is no doubt that the Continental Jay visits England in small numbers
in winter, but not many seem to reach the Midland counties. Altogether only
a few cases have been recorded, but this is probably due to the small number
which have been critically examined. Nearly all the Jays killed in winter which
the senior author has examined are typical rufitergum; but at least one, shot by
Lord Rothschild near Tring, on the boundary of Bucks, and Herts., is an equally
typical G. g. glandarius.
10 (13). STARLING. Sturnus vulgaris vulgaris L.
B. of Berks, and Bucks, p. 38. Vict. Hist, of Bucks, vol. i. p. 138.
Numerous resident.
Though a great many Starlings remain throughout the winter, their number
diminishes somewhat after October, so it would seem that some move southwards.
The flocks of Continental Starlings which arrive in autumn on the east coast
appear not to reach this county. Starlings are now often a great pest to fruit-
growers. There has undoubtedly been an enormous increase in their numbers
during the last half-century, probably owing in a great measure to the diminution
in the numbers of birds of prey. Mr. A. H. Cocks says that he has visited a covert
in the county, used as a roosting-place by large flocks of these birds, which was
entirely swamped in dung, so that nothing could grow in it.
11 (14). ROSE-COLOURED STARLING. Pastor roseus (L.).
Gould, B. Europe, vol. iii. text to pi. 212. B. of Berks, and Bucks, p. 178. Vict. Hist, of Bucks.
vol. i. p. 138.
Rare, straggler.
Only one instance is known to us for Bucks. Gould, I.e., states that a
specimen was shot by John Newman, at Iver Court, near Langley, in Bucks.
12 (15). GOLDEN ORIOLE. Oriolus oriolus oriolus (L).
B. of Berks, and Bucks, p. 170. Vict. Hist, of Bucks, vol. i. p. 134.
Rare summer migrant : no fwoof of breeding.
Mr. Charles Wolley, writing to the Field, May 25, 1861, p. 451, under the
initials " C. W.," states that a nest of this species with four eggs was taken near
Stoke, Bucks., "a few days ago," and that the eggs were still in the possession
of Fisher, the naturalist of Eton. Clark Kennedy adds that the eggs were
purchased by Mr. \V0lIe3', and proved to be the rare variety of the Song-Thrush's
egg, with black markings on a white ground. He also adds that a nest is said
to have been found near Burnham, but gives no details. On May 19, 1879 (not
176 NOVITATES ZOOLOGICAE XXVII. 1920.
1897 as stated in the Vict. Hist. Burks), a male was shot at Stoke Mandeville,
and was recorded by H. White in the Field (May 31, 1879, p. 625). Probably
it is to this occurrence that Mr. T. Marshall refers in a note to the Field (May 16,
1891), in which it is stated that this species was recorded from near Aylesbury
in May 1880.
Finally Mr. A. H. Cocks (in lift, to the authors of the Vict. Hist, list) says,
" This bird has been reported to have nested about three miles north from here
in 1901, the nest and eggs having been taken; but I cannot answer for it
personally."
13 (16). HAWFINCH. Coccothraustes coccothraustes coccothraustes (L.).
B. of Berks, and Bucks, p. 35. Vict. Hist, of Bucks, vol. i. p. 136.
Resident, fairly common in pkiies, though load.
Apparently the numbers of this bird fluctuate, but this may possibly be due
to persecution by gardeners, etc. Nesting near Windsor was recorded by Yarrell
as far back as 1827 ; and Clark Kennedy mentions it as breeding in Windsor Park
(Berks.), at Latimer near Chesham, near Aylesbury, Langley and Stowe Park.
Mr. Heneage Cocks observed its nesting at and near Great Marlow, and Grossman
at Burnham Beeches. It has also been observed at Chequers Court, Weston
Turville, Halton, Newbury, High Wycombe, Cholesbury, Chesham, Drayton,
and St. Leonards (near Tring). Mr. E. E. Pettitt meets with it occasionally in
winter in the Thames Valley, but has not hitherto found it breeding there, though
it is not uncommon as a breeding species in the Maidenhead district, where Major
F. W. Proctor found several nests.
14 (17). GREENFINCH. Chloris chloris chloris (L.).
B. of Berks, and Bucks, p. 34. Vict. Hist, of Bucks, p. 136.
Common resident throughout the year.
Frequents orchards, gardens and hedges, associating in flocks in the winter.
15 (18). BRITISH GOLDFINCH. Carduelis carduelis britannica (Hart).
B. of Berks, and Bucks, p. 36. Vict. Hist, of Bucks, p. 136.
Resident.
The Goldfinch had become scarce, especially in the neighbourhood of Ayles-
bury, Wendover and Tring, about twenty years ago, and the blame for this was
generally put on the bird-catchers, and probably not without reason, as the
Goldfinch is very easily caught in nets and with birdlime. During the last ten
years or so, however, it has increased again in numbers considerably, and may
be frequently seen near the Tring and Halton Reservoirs, near Chesham, Beacons-
field, Cholesbury, Aylesbury, Wendover and Halton, Cheddington and Aston
Abbots.
16 (19). SISKIN. Carduelis spinus (L.).
B. of Berks, and Bucks, p. 109. Vict. Hist. «j Burks, p. 136.
Irregular and rare winter visitor ; said to have bred on one occasion. Few
recent records.
Kennedy tells us that in his time many were caught by the professional
NoVITATES ZOOLOGICAE XXVII. 1920. 177
bird-catchers near Eton and Windsor " every season."* He was informed by
Burgess that it occurred near Chesham and Slapton, and by H. H. Crewe that
a bird-catcher at Drayton Beauchamp " not unfrequently captures the Siskin
in his clap-nets during the winter months, in that neighbourhood."
According to Gould (B. of Great Britain, iii. text to pi. 37, 1873), Siskins
were frequently met with by him in large troops in the woods of Taplow and
Cliefden, especially in the neighbourhood of the lower road by the Thames side.
The winters of 1857 and 1866-67 were noted for the occurrence of this species in
great numbers.
J. Steele- Elliott {Vict. Hist, of Bed fords, i. p. 112 note) points out that the
reported nesting of the Siskin " in Bedfordshire " (Zool. 1880, p. 259) is an error,
and should have been recorded as " in Buckinghamshire." The Rev. H. Burney
(loc. cit.) states that two nests of the Siskin were found on his property in May
1879, and several young reared. The note is headed, " Siskin Nesting in Bed-
fordshire," but Mr. Burney wrote from Wavendon Rectory, Woburn, which is
situated in Bucks. In answer to an appeal for further details, Mr. R. H. Mitford
writes (t.c. p. 364) that Mr. Burney saw a Siskin in a cage in a cottage in his parish.
It was stated to be one of five taken from a nest by a boy, who said that he found
two nests with young in June 1879, one in the fork of a maple, and the other
in a hornbeam. One young bird passed into Mr. Burney's possession, and his
description satisfied Mr. Mitford, who was somewhat sceptical on the subject,
that it was a hen Siskin. The nesting-sites, however, would be quite abnormal
for this species, and more like those adopted by the Lesser Redpoll, so that possibly
the two species were confused. Still more recently, Mr. E. E. Pettitt records
the occurrence of this species near Colnbrook, on March 14, 1897.
17 (20). TWITE. Carduelis flavirostris flavirostris (L.).
B. of Berks, and Bucks, p. Ill (under the name of " Mountain Linnet, Linota montium "). Vict.
Hist, of Bucks, p. 137.
R:tre winter visitor.
Kennedy, who describes this species as a winter visitor, but less abundant
than the Lesser Redpoll, gave no dates whatever. We have specimens caught
near Aston Clinton by a bird-catcher, 21 . xi . 1893, 5 . xii . 1893, and 1 1 . xi . 1898.
Mr. Alfred Heneage Cocks wrote in 1902 that three Twites were caught near
Skirmett in a Pheasant-trap in February 1902.
[HOLBOLL'S REDPOLL. Carduelis linaria holboelli (Brehm).
Vict. Hist, of Bucks, p. 137.
An adult male of this form, with wing 80, tail 62 mm. long, and a very pale
crown, was caught by a bird-catcher near Aston Clinton, December 14, 1895,
and is in the Tring Museum.
It is, however, doubtful if holboelli is a distinct form, as it appears to breed
within the same area as C. I. linaria. (Cf. Pract. Handb. vol. i. p. 60, 1919, also
Nov. Zool. 1920.)]
* It is, however, worth notice that, writing in the Zool. 1867, p. 705, of the occurrence of Siskins
in a bird-fancier's shop at Eton, he states, '"I fancy these birds are not common about here, not
having noticed any before."
12
178 XOVITATES ZOOLOOICAE XXVJI. 1!>20.
18 (22). MEALY REDPOLL. Carduelis linaria linaria (L.).
Vict. Hist, of Bucks, p. 137.
Must occur as irregular and rare winter visitor.
As the Mealy Redpoll is known to visit the Thames Valley, and one has been
taken near Ivinghoe, in Herts., close to the Bucks, boundary, there is no doubt
that it occasionally visits our county.
19 (23). LESSER REDPOLL. Carduelis linaria cabaret (P. L. S. Mull.).
B. of Berks, and Bucks, p. 110. Vict. Hist, of Bucks, p. 137.
Winter visitor, but also breeds locally in small numbers.
Kennedy only records this species as a winter visitor from about the end of
November onwards, and never very common. Hartert on several occasions
has noted small flocks in autumn and winter, and there are several specimens
in the Tring Museum from Aston Clinton, near Tring, caught in October and
November.
Twenty-eight years ago Lord Rothschild observed it several times on the
"flats" near Champneys Park in summer, and Grossman has recorded breeding
on Berkhamsted Common, close to the Bucks, boundary. C. Oldham {in litl.)
states that he has seen a few pairs every summer about the Herts .-Bucks, boundary
near Berkhamsted, and adds that he also saw one at Mentmore on June 15, 1913,
" uttering its trilling song in flight."
The only part of the county where breeding is known with certainty to have
taken place is the Thames Valley between Shiplake and Wraysbury. Many
scattered pairs used to haunt the various " rod beds " by the river, nesting in
most cases on the Berks, side, and sometimes several nests might be found within
quite a small area. The late Major F. W. Proctor found many nests in this
district between 1905 and 1914; not only in willows, but also in thorns, furze
bushes, and small trees at some little distance from the river. Mr. E. E. Pettitt
gives details (in Hit.) of half a dozen Bucks, nests found by him in the same district
between 1909 and 1916, but adds that after the severe winter of 1916-17 none
were met with.
20 (27). LINNET. Carduelis cannabina cannabina (L.).
B. of Berks, and Bucks, p. 37. Viet. Hist, of Bucks, p. 137.
Common resident.
Common apparently everywhere. Very fond of nesting in gorse bushes, in
which the nests may sometimes be found close to each other.
21 (30). BRITISH BULLFINCH. Pyrrhula pyrrhula pileata (MacGill).
B. of Berks, and Bucks, p. 37. Vict. Hist, of Bucks, p. 137.
Resident.
The Bullfinch is common, though persecuted by gardeners on account of
the damage caused by it to fruit-buds.
NOVITATES ZOOLOGICAE XXVII. 1920. 179
22 (33). COMMON CROSSBILL. Loxia curvirostra curvirostra L.
B. of Berks, and Bucks, p. 111. Vict. Hist, of Bucks, p. 137.
Irregular summer and winter visitor, which apparently nests occasionally.
Immigrations take place from time to time, often in great numbers, and birds
may then stop for a year or so and possibly nest. In the old manuscript at
Din ton Hall is an excellent figure of "ye Crossbill or Shellapple" which was
shot there in 1782, with the following notes : " Is an inconstant visitor of this
island and breeds in ye pine-forests of Germany and Switzerland ; it feeds on ye
cones of those trees. It is a fact that it changes ye shades of its colour in different
seasons of ye year from deep red to yellow and ye females which are greenish
alter to different varieties of the same colour. Ten of these birds were shot and
several others seen by ye Revnd W. Goodall in ye Wilderness of Dinton Hall
August 8th' 1791. They had been observed by the servants some weeks, tho'
they mistook them for bull finches. Q>T had they bred there ? As some of ye
males had not then gained their full j^lumage and one of ye females had not as
yet a single yellow feather." It is, of course, well known now that the red
plumage is that of the adult male, though peculiar ideas about the plumages
of Crossbills prevail occasionally even now.
Kennedy records occurrences at Drayton (about 1847), and also at Fulmer,
Risborough, and Burnham Beeches, and mentions a hen bird seen near Eton in
November 1867.
More recently T. Marshall recorded this species in the Wycombe district in
1898 (Field, December 3, 1898, p. 897) ; while in December 1909 a flock of about
thirty was seen at Fawley Court (H. Noble, Brit. Birds (mag.), vol. iii. p. 303).
In March 1910 six were seen at Drayton Beauchamp (C. Oldham, i.e. p. 409),
and several at Langley about the same time (H. Noble). A pair killed at Dinton,
January 15, 1910, is in the County Museum (Edw. Hollis).
The only definite record of breeding is that by Mr. R. Bulstrode (Brit.
Birds (mag.), vol. vi. p. 60), who saw a flock of four or five birds near Gerrards
Cross on March 27, 1910, and was shown a nest on April 1 which then contained
four eggs. The young were still in the nest on April 23.
23 (37). CHAFFINCH. Fringilla coelebs coelebs L.
B. of Berks, and Bucks, p. 31. Vict. Hist, of Bucks, p. 136.
Resident, but numbers apparently augmented by immigrants in winter.
Very common in all wooded parts of the county.
Mr. A. Mayall found eight eggs in a nest near Burnham, from which six
young were reared, in May 1919 (Brit. Birds, vol. xiii. p. 80).
24 (38). BRAMBLING. Fringilla montiMngilla L.
B. of Berks, and Bucks, p. 106. Vict. Hist, of Bucks, p. 136.
Winter visitor, sometimes in great numbers.
The Brambling appears every winter, and has been observed from October
to April, but generally between November and March. Numbers vary greatly,
sometimes not many are observed, while in other years they are very numerous ;
Hartert does not think that this depends on the severity of the winter — at least
not in this country — but more on the amount of beech mast. From time to time
180 NOVITATES ZOOLOGICAE XXVII. 1920.
enormous flights are observed. An influx of this kind took place in the winter
of 1905-6, when the beech woods of the Chilterns swarmed with these birds,
flocks of several hundreds being repeatedly seen. Considerable numbers were
also present during the mild winter of 1919-20.
25 (40). HOUSE-SPARROW. Passer domesticus domesticus (L.).
B. of Berks, and Bucks, p. 33. Vict. Hist, of Bucks, p. 136.
Common resident.
By far the most numerous of all birds in the county. One of the most
obnoxious habits of this species is that of dispossessing the House-Martins of their
homes. Sir. A. H. Cocks adduces some evidence that the Martins occasionally
retaliate by killing the nestling Sparrows, but further evidence on the point is
desirable (cf. Zool. 191G, p. 358).
26 (41). TREE-SPARROW. Passer montanus montanus (L.).
B. of Berks, and Bucks, p. 32. Vict. Hist, of Bucks, p. 136.
" A resident species, but noichere numerous and very local."
The above words of Kennedy are still correct and well describe the status
of this bird in Bucks. Kennedy reports a nest near Buckingham in a Sand-
Martin's hole. He also mentions specimens killed near Datchet and Slough.
From autumn to spring, however, Tree-Sparrows are common in the neighbour-
hood of Wendover, Aston Clinton, Ivinghoe, where Oldham regularly observes
them, usually feeding with House-Sparrows and Finches in farm-yards and stack-
yards, and near Cheddington, but they are seldom seen in the summer. Mr.
Oldham observed one near Cheddington May 10, 1908. Hartert has seen it near
Aylesbury and Ovington.
In the Thames Valley there are scattered colonies, which nest in the pollarded
willows by the river-side, especially in the Maidenhead and Bray districts. Mr.
Pettitt mentions a small colony at Horton.
27 (42). CORN-BUNTING. Emberiza calandra calandra L.
B. of Berks, and Bucks, p. 29. Vict. Hist, of Bucks, p. 137.
Resident,
Not actually rare in the arable districts, but nowhere numerous, and not
often noticed in winter. Kennedy (I.e.) says " it congregates in large numbers
late in the autumn and is gregarious until the return of the spring." We have
never seen large flocks in Bucks, or Herts.
In the Thames Valley Mr. Pettitt notes it as breeding near Taplow, Slough,
and the reservoirs on the Middlesex border.
F. A. Monckton has recorded a case in which the song was heard in November
near Eton {Field, November 14, 1908, p. 888).
28 (43). YELLOW BUNTING, or YELLOWHAMMER. Emberiza citaneUa
citrinella L.
B. of Berks, and Bucks, p. 30. Vict. Hist, of Bucks, p. 18.
Resident.
A common bird, but somewhat diminished in numbers since 1917. Mr. A. H.
Cocks records a nest built in the side of a straw-rick, about 3 ft. 7 in. from the
NOV1TATES ZOOLOGICAE XXVII. 1020. 181
ground at Skirmett (Zool. 1916, p. 352), but this is not a very infrequent
occurrence.
29 (47). CIRL-BUNTING. Emberiza cirlus cirlus L.
B. of Berks, and Bucks, p. 176. Vict. Hist, of Bucks, p. 138.
Resident.
The Cirl-Bunting breeds regularly in the Chiltern Hills district and neigh-
bourhood. In winter it strays about, but apparently not usually very far from
its breeding-grounds. The following are the localities from which we have
evidence : Terriers End, near Tring (Chas. Oldham, evidently nesting) ; neigh-
bourhood of Wendover (Hubert D. Astley, Oldham, Witherby, Hartert, nesting) ;
Ashley Green, south of Berkhamsted, Coombe Hill, Chequers Court (Hubert I>.
Astley, nesting) ; Drayton Beauchamp (4 . vi . 1864, nest found by H. H. Crewe,
Field, 3 . xii. 1864, p. 384) ; Halton (skins of winter birds, eggs seen) ; Pitstone
(caught in winter, H. H. Crewe) ; Ivinghoe (seen in winter, Hartert) ; downs
between Princes Risborough and Wendover common, five males singing between
Kimble and Wendover 4.vii.l910 (Chas. Oldham). In the Thames Valley it
is of infrequent occurrence, but has been met with occasionally near Great
Marlow. Mr. A. H. Cocks records one from Harleyford on January 26, 1884
(in lift.). The winter of 1917 has greatly diminished the number of Cirl-Buntings ;
near Tring we have not heard or seen them since.
30 (53). REED-BUNTING. Emberiza schoeniclus schoeniclus L.
B. of Berks, and Bucks, p. 29. Vict. Hist, of Bucks, p. 138.
Resident, but breeding birds wander about in autumn.
Not rare in suitable places on rivers and reservoirs. Breeds on the Tring
and Halton Reservoirs, on the banks of the Thames, Colne, Chess, and Ouse,
and in Stowe Park. In winter in small flocks, which haunt stack-yards and high-
roads.
Mr. E. E. Pettitt found a nest of this species in June 1905 at Wraysbury,
which was placed in the crown of a pollarded willow ! He has also on two
occasions met with Cuckoos' eggs in Reed-Buntings' nests in the county, both
in 1908, in the Colne Valley.
A very remarkable clutch of four eggs, pale blue without any markings,
was taken by James Street at Mars worth Reservoir on May 9, 1910, and is now
in the Tring Museum.
31 (56). SNOW-BUNTING. Plectrophenax nivalis (L.).
Vict. Hist, of Bucks, p. 138.
Winter visitor.
Of somewhat rare and irregular occurrence in winter. The MS. in Dinton
Hall mentions its occurrence there on January 8, 1776. Flocks have repeatedly
been seen near Aston Clinton, and in 1895 near the Tring Reservoirs. On
November 4, 1901, a male was shot at Drayton Lodge, Bucks., between Aston
Clinton and Tring, by Mr. Henry Jenney. (February 22, 1894, another male
was caught near Tring, between Tring and Aston Clinton, just in Herts.)
Mr. C. H. Enison met with two on Ivinghoe Beacon on November 7, 1903
(Field, November 14, 1903, p. 844).
182 NOTITATES ZOOLOOICAE XXVII. 1920.
32 (61). WOODLARK. Lullula arborea arborea (L.).
B. of Berks, and Bucks, p. 29. Vict. Hist, of Bucks, p. 139.
Probably resident.
Local and scarce. Observed in spring and summer near Fulmer, Beacons-
field, Princes Risborough, Halton, and Chequers Court.
33 (62). SKYLARK. Alauda arvensis arvensis L.
B. of Berks, and Bucks, p. 27. Vict. Hist, of Bucks, p. 139.
Resident.
Common on fields and meadows, from autumn to spring in flocks, which are
probably partly composed of continental visitors. Breeds freely both in corn and
grass land. An entirely buff- yellow variety was shot in December 1863 at
Weston Turville (R. Tyrer, Zool. 1864, p. 8957). Such varieties are not rare
and have been observed in many other places in England and elsewhere.
34 (67). TREE PIPIT. Anthus trivialis trivialis (L.).
B. of Berks, and Bucks, p. 8G. Vict. Hist, of Bucks, p. 134.
Summer resident.
Not rare in wooded districts from April to September, but far from numerous
in the Thames Valley, where, however, a few pairs may be found breeding in the
Burnham and Taplow districts.
35 (68). MEADOW PIPIT. Anthus pratensis (L.)
B. of Berks, and Bucks, p. 27. Vict. Hist, of Bucks, p. 134.
Resident and winter visitor.
Nests in lowland pastures : on the canal banks near the Tring Reservoirs,
Halton, Aylesbury, Buckingham, Castlethorpe, Farnham Common, Burnham
Beeches, and, according to Kennedy, near Eton. In winter and during migration
periods in small flocks near the Reservoirs. In the Thames Valley it is best
known as a winter visitor, only a few pairs remaining to breed.
36 (74). BLUE-HEADED WAGTAIL. Motacilla flava flava L.
Once observed.
" In a pasture bordering one of the reservoirs near Tring, on April 29, 1917,
my sister-in-law detected a Wagtail differing in colour from the Ray's Wagtails
with which it was consorting. As we looked down from the top of the reservoir
embankment on the birds running to and fro in the short grass, it was an easy
matter to distinguish the stranger by its blue-grey crown and nape, the con-
spicuous whitish-buff superciliary stripe, the less distinct streak of the same
colour through the ear-coverts, and the buff wing-bars. The upper parts and
ear-coverts were greyish-brown, the breast and belly pale yellowish-buff passing
into bright sulphur- yellow on the under tail-coverts. I cannot say positively to
which subspecies of Motacilla flava the bird (a hen) belonged, but the blue- grey
crown and the pale ear-coverts point to M. f. flava, the subspecies, apart from
Novitates Zooloqicae XXVII. 1920. 183
M. j. rayi, most likely to occur" (Chas. Oldham, Brit. B. vol. xi. p. 20, 1917).
There is also a female in the County Museum, found dying near Aylesbury,
June 2, 1911 (Edwin Hollis, in litt.).
37 (79). YELLOW or RAY'S WAGTAIL. Motacilia flava rayi(Bp.).
B. of Berks, and Bucks, p. 85 (not 58). Vict. Hist, of Bucks, p. 134.
Summer resident.
Not a common bird, but more frequent in low-lying meadow land and
in the neighbourhood of rivers, such as the Thames and Ouse.
38 (80). GREY WAGTAIL. Motacilia cinerea cinerea Tunst,
B. of Berks, and Bucks, p. 26. Vict. Hist, of Bucks, p. 134.
A breeding species in very small numbers in the Chess Valley, otherwise winter
visitor, not common.
The first mention of the breeding of this species in Bucks by John Gould
occurs in Jardine's Contr. to Ornith. 1849, p. 137, and is repeated in his Birds of
Great Britain, vol. iii. p. 49 (1873), where he states that for many years he has
been aware of the breeding of the Grey Wagtail in the Chess Valley, and that
when the Duke of Bedford " favoured him with a day's fishing," he found the
nest on a wall of Mrs. Dodd's beautiful garden, where it always nested. Another
pair also bred at Latimer, but in this case he did not find the nest.
R. B. Sharpe, in his articles on the " Birds of Cookham," (Quart. Mag.
High Wycombe Nat. Hist. Soc. vol. ii. p. 49, 1869), alludes to Gould's discovery
of this nest in- a rose bush against the wall, and the fact of the male bird being
found on the four eggs. He also says that another pair bred at Elliot's Mill,
two and a half miles up stream. Clark Kennedy (I.e.) was apparently unaware
of Gould's observations, but says that a few have been procured on the Thames
in summer, though it is better known there as a frequent winter visitor. Bryant
Burgess, however, informed him that it bred annually on the banks of the Chess.
Hartert did not meet with it at Latimer in 1902, but more recent observations
by the Duchess of Bedford and Mr. W. Bickerton show that it still frequents
its old haunts at Chenies. near Sarrat Mill, some distance below Latimer, where,
however, it was not found in 1918, while no observation took place in 1919.*
To other parts of the county it is only known as a winter visitor. Mr. C.
Oldham states that it frequents the reservoirs, canals, and water-cress beds of
North Bucks in small numbers regularly from early September to mid-March.
The Rev. H. D. Astley has recorded it from Chequers Court, and it is met with
every winter in the Thames Valley.
39 (81). PIED WAGTAIL. Motacilia alba lugubris Temm.
B. of Berks, and Bucks, p. 26. Vict. Hist, of Bucks, p. 134.
Resident, but a good many move southwards in the autumn and return in early
spring.
A common bird, and widely distributed.
* The breeding-place near Sarrat Mill, close to Chenies, is just a stone's throw or so outside
Bucks., in Herts., while Latimer and Chenies are well within the Bucks, boundary.
184 N0Y1TATES ZOOLOGICAL XXVII. 1920.
40 (82). WHITE WAGTAIL. Motacilla alba alba L.
B. of Berks, and Bucks, p. 134.
Rare on passage ; has apparently once bred.
On June 17, 1902, Hartert and Arthur Goodson went along the River Chess,
near Latimer, in search of the Grey Wagtail. They failed to find the latter,
but saw a pair of Wagtails feeding young which seemed to have quite grey backs,
and which they took to be M. alba alba. A few hundred yards away they observed
M. alba Ittgubris. On subsequent visits later in the year and in 1903 and l!iii4
Hartert failed to see any grey-backed birds. Recently Mr. Chas. Oldham has
observed the White Wagtail in spring, though not nesting. On May 5, 1912,
he saw one on Wilstone Reservoir ; on May 4, 1913, one with a party of the Yellow
(Ray's) Wagtails at Startops End Reservoir ; and on May 3 and 10, 1914, a single
one on Wilstone Reservoir.
41 (83). BRITISH TREE CREEPER. Certhia familiaris brittanica Ridgw.
B. of Berks, and Bucks, p. 49. Viet. Hist, of Bucks, p. 133.
Resident.
Used not to be rare, but has greatly diminished in number since the severe
winter of 1917.
42 (86). BRITISH NUTHATCH. Sitta europaea britannica Hart.
B. of Berks, and Bucks, p. 50. Vict. Hist, of Bucks, p. 133.
Resident.
Not uncommon in well-timbered parts of the comity, particularly in Burnharn
Beeches and Ashridge Park, but somewhat local and not very numerous any-
where.
43 (88). BRITISH GREAT TIT. Parus major newtoni Prazak.
B. of Berks, and Bucks, p. 23. Vict. Hist, of Bucks, p. 133.
Resident.
Generally the commonest of our Titmice. Though greatly reduced in 1917,
increasing again rapidly in numbers.
44 (90). BRITISH BLUE TIT. Parus caeruleus obscurus Prazak.
B. of Berks, and Bucks, p. 24. Vict. Hist, of Bucks, p. 133.
Resident.
Common, and apparently in many places scarcely less numerous than the
' Great Tit.
45 (92). BRITISH COAL-TIT. Parus ater britannicus Sharpe & Dress.
B. of Berks, and Bucks, p. 24. Vict. Hist, of Bucks, p. 133.
Resident.
Fairly common in woods, parks, orchards, and gardens, especially where
conifers are grown. Though the species suffered greatly during the severe cold
of 1917, it is already increasing remarkably.
Novitates Zoolooicae XXVII. 1920. 185
46 (97). BRITISH MARSH-TIT. Parus palustris dresseri Stejn.
B. of Berks, and Bucks, p. 25. Vict. Hist, of Bucks, p. 133.
Resident.
Used to be fairly common, but has become much rarer since the severe frost
of 1917. It is, however, increasing again in numbers.
47 (98). BRITISH WILLOW-TIT. Parus atricapillus kleinschmidti Hellm.
The only record for Bucks of which we are aware is a male, formerly in the
collection of H. H. Slater (now in the Tring Museum), shot by him at " Chersley,
Bucks, 9.xi.l882.'' It was, of course, labelled by the collector as "Parus
palustris," as at that time it was not yet distinguished, but is undoubtedly the
present form.
48 (101). BRITISH LONG-TAILED TITMOUSE. Aegithalos caudatus roseus (Blyth).
B. of Berks, and Bucks, p. 25. Vict. Hist, of Bucks, p. 133.
Resident.
Used to be found in practically all suitable localities, but suffered greatly
during the severe frost of 1917. Near the Tring Reservoirs it bred year after
year, but has been exterminated in that neighbourhood and not yet seen again.
Prior to 1917 it used also to nest fairly commonly at Burnham Beeches,
Ditton Park, etc., but has disappeared almost entirely from that district (E. E.
Pettitt). As it is beginning to recover its former status in Berks., it will probably
reappear in these localities before long.
49 (103). BRITISH GOLDCREST. Regulus regulus anglorum Hart.
B. of Berks, and Bucks, p. 23. Vict. Hist, of Bucks, p. 132.
Resident.
Used to be fairly common in suitable localities, but has suffered greatly by
the severe frost of 1917, and is now a rare bird. On July 28, 1918, Chas. Oldham
heard one singing in the shrubbery at Aston Clinton Park, and another in the
park at Ashridge on January 18, 1919 — the only two he has come across since
the winter of 1916-17. Hartert has only seen a few near Tring, but not yet in
Bucks., since 1917. In the south of the county it was formerly not uncommon,
breeding in the Thames Valley at many points, but is only just beginning to
reappear in small numbers.
50 (104). FIRECREST. Regulus ignicapillus ignicapillus (Temm.).
B. of Berks, and Bucks, p. 173. Vict. Hist, of Bucks, p. 132.
Exceptional winter visitor.
Mr. Alfred Heneage Cocks informed us in 1902 of a specimen killed by his
gardener, in his and his brother's presence, at Great Marlow in the sixties, about
1863. It was mounted and is in Mr. Cocks's possession, but it was only identified
as a Fireerest some years after.
According to Kennedy (I.e.), two Firecrests were procured near Eton about
1 865. This record is rather vague, and as soon after it is stated that a nest with
1S6 N0V1TATES ZOOLOGICAE XXVII. 1920.
young, and the two parents, were brought to a Mr. Hasell in 1863, from Windsor
Park, and the latter statement cannot be credited, the Eton record can hardly
be accepted without caution. In Trans. Herts. Nat. Hist. Soc. vol. v. p. 82, it is
stated that one was shot in January 1887, presumably at the Reservoirs. This
statement, said to have been made on the authority of the then Hon. Walter
Rothschild, is evidently erroneous, as all the supposed author remembers is a
verbal statement made to him by the late Rev. H. H. Crewe that it had occurred
in Ashridge Park.
51 (105). BEARDED TITMOUSE. Panurus biarmicus biarmicus (L.).
B. of Berks, and Bucks, p. 174.
Exceptional vagrant — one old record.
On December 21, 1848, a pair, male and female, were shot on Wilstone
Reservoir by the Rev. James Williams, of Tring Park. Only these two specimens
were observed, and there is no other record of the occurrence of this species
{Zoologist, 1849, p. 2418.) (About twenty years ago some specimens imported
from Holland were released on Wilstone Reservoirs, but they disappeared.)
52 (107). GREAT GREY SHRDSE. Lanius excubitor excubitor L.
B. of Berks, and Bucks, p. 168. Vict. Hist, of Backs, p. 134.
Irregular and rare winter visitor.
On January 8, 177S, one was shot near Dinton Hall. A female was shot
near Wendover about the middle of November 1854, and a male on November 4
of the same year near Weston Turville (H. H. Crewe, Zoologist, 1865, p. 9416).
In the winter of 1859-60 a specimen was shot on the banks of the Thames near
Clewer, Berks. According to Kennedy (I.e.), a male was shot in 1862 near the
Almshouses at Stoke, another in the winter 1865-66 on the banks of the Thames
near Windsor, a third at Hampden (no date) which was in Bryant Burgess's
collection. Mr. A. H. Cocks also reports one shot close to Great Marlow, either
in the eighties or early in the nineties. Hartert saw one in October 1895 near
Halton. A female was shot by the present Lord Rothschild on the " Flats "
close to the Bucks, boundary near Cholesbury, 17.x. 1895; a male by a keeper
near Long Marston, also close to the boundary, 1 8 . xi . 1 896 ; another female caught
in a Sparrow-trap at Wilstone Reservoir, 2 . ii. 1 916.
53 (112). RED-BACKED SHRIKE. Lanius collurio collurio L.
B. of Berks, and Bucks, p. 72. Vict. Hist, of Bucks, p. 134.
Summer resident.
Rather local and less common during the last twelve years or more than it
used to be. In Kennedy's time it was common near Eton. Hubert D. Astley
found it not rare near Chequers Court ; and Hartert has observed it there and near
Wendover, Aston Clinton, Aylesbury, Buckingham, Dinton, Newport Pagnell,
Castlethorpe, Wingrave, and Aston Abbots, but has not seen it recently near
Wendover and Aston Clinton in places where it always used to be in evidence.
Near the Reservoirs only about one pair has nested recentty. In the Thames
Valley it is rather local, but Mr. Pettitt reports a few pairs breeding near Colne-
brook, Horton, and Little Marlow.
NOVTTATES ZOOLOOICAE XXVII. 1920. 187
54 (113). WAXWING. Bombycilla garralus (L.).
B. of Berks, and Bucks, p. 174. Vict. Hist, of Bucks, p. 135.
Irregular and rare winter visitor.
Kennedy (I.e.) writes : " An immense flock appeared along the eastern shores
of our island in the winter of 1849-50, which was very severe, and several speci-
mens were at that time procured in different parishes of Buckinghamshire. I am
indebted to the Rev. Bryant Burgess for the notice of a Bohemian Waxwing
which was killed at Ivinghoe Aston in January 1850, and which is now in his
collection. An immense number of Bohemian Waxwings were shot in the neigh-
bourhood of Buckingham during the spring of 1867, as Mr. J. W. Thorpe told me."
[In Trans. Herts. Nat. Hist. Soc. vol. v. p. 82, in a list of birds supposed to
have occurred on the Reservoirs, it is stated that a Waxwing was " obtained in
March 1883." Unfortunately this statement, made on the authority of the
Hon. Walter Rothschild, cannot now be verified, as we cannot trace the specimen.
In the Vict. Hist, of Herts, p. 201, it is said that " the first Hertfordshire specimen
of the Waxwing was shot about a mile from Tring on the Aylesbury road, about
1851." As the Bucks boundary is very little more than a mile from Tring, this
may almost be regarded as a Bucks record.]
55 (114). SPOTTED FLYCATCHER. Muscicapa striate striate (Pall.).
B. of Berks, and Bucks, p. 74. Vicl. Hist, of Bucks, p. 135.
Summer resident.
Common everywhere in parks, large old gardens, and certain woods.
The blue unspotted type of egg has been found near Slough (H. H. Vyse,
Zool. 1890, p. 352, and Field, August 16, 1890, p. 250).
56 (116). PIED FLYCATCHER. Muscicapa hypoleuca hypoleuca (Pall.).
B. of Berks, and Bucks, p. 169. Vict. Hist, of Bucks, p. 135.
Probably occasional summer resident.
The records for Bucks, are very few. According to Morris one was killed
" many years ago " in the county, in the south-east, not far from Uxbridge.
H. J. Elwes informed Kennedy of a well-authenticated nest taken near Eton in
the summer of 1860. Mr. Heatley Noble, in litt. : "A nest with six eggs was
taken on my late father's property, Berry Hill, Taplow, in June, 187- (the exact
year cannot be given). The female was unfortunately killed on the nest." Mr.
H. Heneage Cocks, in litt., says : " On May 12, 1883, our gardener at Great
Marlow saw in our orchard a bird with white on the wings, which, from its move-
ments and other habits, must have been a Flycatcher. He said it looked some-
what like a female Chaffinch, but the beak was different. Sir J. A. Godley,
K.C.B., reported several years before having seen one specimen there. Two days
afterwards the gardener saw evidently the pair, but though I watched for them
repeatedly I did not see them, nor were they ever seen again." On May 10,
1901, Hartert heard the song and observed a male in the park of Mentmore.
In June of the same year he found no trace of these birds, nor ever afterwards.
Mr. Edwin Hollis, while fishing at Hartwell, August 22, 1919, saw a male
Pied Flycatcher. It was quite clearly recognized, as it sat within 8 or 10 feet
of the observer for several minutes.
188 NOVITATES ZOOLOGKAE XXVII. 1020.
57 (119). CHIPFCHAFF. Phylloscopus collybita collybita (Vieill.).
B. of Berks, and Bucks, p. 85. Vict. Hist, of Bucks, p. 132.
Summer resident and autumn migrant.
Common in all suitable localities. From February 10 to 18 a Chiffchaff
frequented some willows on Wilstone Reservoir. (See Brit. B. vol. vi. p. 313.)
In the Thames Valley it is generally distributed, and Mr. Pettitt notes it
as especially numerous in Ditton Park.
58 (122). WILLOW- WARBLER. Phylloscopus trochilus trocbilus (L.).
B. of Berks, and Bucks, p. 84. Vict. Hist, of Bucks, p. 132.
Summer resident ami passage migrant.
Generally distributed and hardly absent from any suitable localities.
59 (125). WOOD- WREN or WOOD- WARBLER. Phylloscopus sibilate sibilatrix
(Bechst.).
B. of Berks, and Bucks, p. 84. Vict. Hist, of Bucks, p. 132.
Summer resident.
The Wood-Wren occurs from April to September in beech and oak woods,
in the Chilterns and near Brickhill. In the Thames Valley it is decidedly scarce
and entirely absent from the greater part of the district. Mr. Grossman, however,
states that it was formerly fairly plentiful in Burnham Beeches and in the woods
between that place and Ashley Green ; but Mr. Pettitt has failed to meet with it
breeding. A few pairs, however, haunt the woods near the western boundary
where the county is more hilly.
[SAVI'S WARBLER. Locustella luscinioides luscinioides (Savi).
B. of Berks, and Bucks p. 172.
In the Zoologist, 1867, p. 704, Lord Clifton published a note saying that he
believed that he had observed a Savi's Warbler in a low hedge near Eton, but his
description of the bird he saw is by no means convincing ; in fact the statement
cannot be accepted. As is well known, the species was formerly a summer resident
in Norfolk, Cambridgeshire, and Huntingdon, but, except for a single bird obtained
on Fair Isle (!) in 1908, has not been proved to occur since 1856.
Another rather vague record appeared in Saunders' Manual Brit. B. ed. ii.
p. 92 (1899), as follows : " There is some evidence that this species was noticed
in May 1897, in the Humber district, as well as near Olney, Bucks. ': The latter
statement refers to an observation by Mr. C. J. Wilson, M.B.O.U., who kindly
wrote to Hartert that he is fully convinced that the " Savi's Warbler is a just
record," because he was close to the bird for some minutes, and the locality, the
appearance, and the note of the bird were all in favour of its being L. luscinioides.]
60 (133). GRASSHOPPER- WARBLER. Locustella naevia naevia (Bodd.).
B. of Berks and Bucks p. 78. Vict. Hist, of Bucks, p. 132.
Summer resident.
Rather rare. The only certain localities we know of are : on the foot of
the hills east of Halton (heard and seen by Arthur Goodson and Ernst Hartert),
NOTITATES ZOOLOGICAE XXVII. 1920. 189
Aylesbury (eggs seen by Hartert), Mentmore (heard by Hartert), Castlethorpe
(observed by the late Lionel Wiglesworth), Farnham Common (observed by Alan
Crossman), Chesham and High Wycombe (teste Kennedy), Drayton Beauchamp
(Kennedy, probably from information of Harpur Crewe). In the Thames Valley
it is a rare visitor, but Mr. E. E. Pettitt discovered a nest with five eggs at Hythe
End in May 1894. Breeding also took place there in 1904, as well as at Wrays-
bury in 1919. Mr. Pettitt notes the arrival of this species in the county on April
22, 1895, April 19, 1900, April 21, 1905, and April 30, 1910. In 1919 a pair nested
close to Marsworth Reservoir, and the nest was found by Mrs. Oliver Pike, and
some beautiful photographs taken by her busband. Mr. Pike is convinced that
there were two pairs, but only one nest was found. The Grasshopper- Warbler
had not occurred in this place during the last twenty-five years or more.
61 (136). REED-WARBLER. Acrocephalus scirpaceus scirpaceus (Herm.).
B. of Berks, and Bucks, p. 80. Vict. Hist, of Bucks, p. 132.
Summer- resident.
Very common on the Marsworth, Wilstone, and Halton (Weston Turville)
Reservoirs, and also on the Rivers Thames, Colne, Chess, and Ouse, wherever reeds
abound. On the Tring Reservoir the Reed- Warbler is the usual and apparently
only foster-parent of the Cuckoo, and all Cuckoo's eggs found there for the last
twenty-five years are of much the same type, of course with some variations.
Along the Thames and Colne Valleys it breeds commonly, as well as on the
pond at Burnham Beeches. Mr. Pettitt has on two occasions found two Cuckoo's
eggs in a Reed- War bier's nest in Bucks.
For a note on unusually early nesting of this species at the Tring Reservoirs,
see Brit. Birds (mag.), vol. ix. p. 48.
62 (137). MARSH- WARBLER. Acrocephalus palustris (Bechst.).
Bred in 1909.
(In Trans. Herts. Nat. Hist. Soc. vol. v. p. 76, it was stated, on the authority
of the Hon. Walter Rothschild, that a Marsh-Warbler was shot near the Mars-
worth Reservoir in August 1883, and was in the Tring Park collection. This
statement seems to be due to an error in identification of a young Reed- Warbler.)
At the time of the publication of the Vict. Hist, of Bucks, this species had not
been ascertained to breed in the county. In 19C9 Mr. G. W. Kerr, who had
previously discovered the Marsh- Warbler breeding in Surrey, was fortunate in
discovering a nest with two eggs of this species, and also one of the Cuckoo in
a dense nettle- bed not far from Magna Charta Island on June 1 4. The nest was
about 12 yards from the river on firm ground, woven round two nettle stems,
and about 18 in. from the ground in the parish of Wraysbury. (The locality in
Surrey where the nest was foimd in 1907 is only a few miles south of the county
boundary, and about five miles distant from where the birds were found breeding
in 1909.) Subsequently Mr. E. E. Pettitt found a second nest at Wraysbury in
the same nettle- bed, containing four Marsh- Warbler's eggs and one of the Cuckoo,
on June 30, 1909, but the Cuckoo's egg was of a different type to that found on
June 14 (Zool. 1909, p. 397).
190 NOV1TATES ZOOLOGICAE XXVII. 1920.
63 (139). SEDGE-WARBLER. Acrocephalus schoenobaenus (L.).
B. of Berks, and Bucks, p. 78. Vict. Hist, of Bucks, p. 132.
Summer resident.
The Sedge-Warbler is generally distributed in the valleys, in the neighbour-
hood of rivers, ditches, reservoirs and ponds, sometimes in thickly over-grown
hedgerows quite a distance from water. Yarrell states that a single specimen was
observed near High W^conibe in winter, without giving full date. Such a state-
ment is hardly acceptable without proof, but curiously enough there are other
statements of the occurrence of Sedge- Warblers in winter.
64 (145). GARDEN- WARBLER. Sylvia borin (Bodd.).
B. of Berks, and Bucks, p. 82. Vict. Hist, of Bucks, p. 131.
Summer resident.
In similar places to the Blackcap, but far less common. Grossman and
Hartert have observed it near Chesham, Beaconsfield, Burnham Beeches, Halton,
Aylesbury, Buckingham, Mentmore, Ashridge Park, Castlethorpe, and Newport
Pagnell ; but it occurs doubtless in many other places. In the Thames Valley
it breeds in suitable spots, but in far smaller numbers than the Blackcap. Mr.
E. E. Pettitt found a nest in Ditton Park which contained a young Cuckoo about
four days old on June 5, 1906.
65 (146). BLACKCAP. Sylvia atricapilla atricapilla (L.).
B. of Berks and Bucks, p. 82. Vict. Hist, of Bucks, p. 131.
Summer resident.
Common in parks, woods with undergrowth, gardens and spinneys. Gener-
ally arrives end or middle of April, but Hartert. has heard it in full song on April
10, near Wilstone Reservoir.
66 (147). WHITETHROAT. Sylvia communis communis Lath.
B. of Berks, and Bucks, p. 83. Vict. Hist, of Bucks, p. 131.
Summer resident.
Common in suitable localities, such as hedgerows, commons, edges of woods,
and some gardens.
67 (148). LESSER WHITETHROAT. Sylvia curruca curruca (L.).
B. of Berks and Bucks, p. 83. Vict. Hist, of Bucks, p. 131.
Summer resident.
The Lesser Whitethroat is generally less numerous than the Whitethroat,
but not a rare bird. It is curious that it should be so much more plentiful in
Middlesex than in the adjoining parts of Bucks.
68 (155). FIELDFARE. Turdus pilaris L.
B. of Berks, and Bucks, p. 105. Vict. Hist, of Bucks, p. 130.
Winter visitor.
Arrives usually in October or even November, but there are records by Lord
Rothschild and others for September ; getting scarcer from end of March, and
Novitates Zoolooicae XXVII. 1920. 191
usually leaving before the end of April, but Crossman mentions ( Vict. Hist. Herts.
p. 196) some seen at Great Gaddesden, on the boundary of Herts, and Bucks., on
May 8, 1887.
69 (156). MISTLE-THRUSH. Turdus viscivorus viscivorus L.
B. of Berks, and Bucks, p. 12. Vict. Hist, of Bucks, p. 129.
Resident.
Common in woods and parks over the greater part of the county, but not in
any great numbers in the Thames Valley.
70 (157). BRITISH SONG-THRUSH. Turdus philomelos clarkei Hart.
B. of Berks, and Bucks, p. 13. Vict. Hist, of Bucks, p. 129.
Common resident.
The British Song-Thrush is even more numerous than the Blackbird, and
stays in Bucks, throughout the year, but a fair number pass through in the autumn,
and some in the spring, evidently from higher ground in the north of England and
Scotland. We have not been able to detect a specimen of the Continental Song-
Thrush among them. The number of Song-Thrushes diminished very greatly
in the severe winter of 1917, and though they have increased again considerably
in numbers, they are still far behind their strength of before 1917.
In the Newton collection at Cambridge is a clutch of four eggs of this species,
taken near Stoke in May 1861, in which the ground-colour is perfectly white,
with the usual markings. They were at first recorded as eggs of the Golden
Oriole. See Ootheca Wolleyana, vol. ii. p. 288, and Field, May 25, 1861, p. 451.
71 (159). REDWING. Turdus musicus L. 1758.
[Turdus iliacus L. 1766, of most authors.]
B. of Berks, and Bucks, p. 106. Vict. Hist, of Bucks, vol. i. p. 130.
Common winter visitor.
Generally arriving about the middle of October and leaving towards end of
March. Mr. Heneage Cocks formerly reported a specimen shot at Harleyford on
July 28, 1871, and Mr. E. Burton Durham records one picked up in September
1913 at Chesham Bois (Field, September 27, 1913).
On March 11, 1906, Mr. A. H. Cocks met with an enormous flock of this
species resting in some meadows near Skirmett. The birds were thickly distri-
buted over eight acres of grass land, so that allowing for one bird to each square
yard, there must have been over 38,000 birds present !
In the cold winter of 1917 all or nearly all Redwings which were in the county
at that time perished ; but in the following winter, though scarcer than usual,
more Redwings were seen than Fieldfares. The cold winter of 1854, according to
the Field, also destroyed Redwings and Fieldfares " by tens of thousands." In
1918 Redwings were generally very scarce. Hartert saw none until March,
when he came to a place — a shrubbery of evergreens — where hundreds were
roosting. In 1919 they were probably about as common as before the severe
frost, and hundreds came to roost in the same place as the winter before, at least
from January to March.
192 Novitates Zoolooicae XXVII. 1920.
72 (162). RING-OUZEL. Turdus torquatus torquatus L.
B. of Berks, and Bucks, p. 136. Vict. Hist, of Bucks, p. 130.
Passage migrant.
Kennedy (I.e.) mentions a specimen shot at Risborough " in the spring " of
1840, and another observed by Burgess in his garden at Latimer, September 9,
1862. when specimens were also seen near Dundridge and Wendover. In Trans.
Herts. Nat. Hist. Soc. vol. v. p. 82, specimens supposed to have been killed in July
1886, and in October of the same year, are mentioned. The former statement is
probably incorrect, being from hearsay or recollection. In 1865 a male was killed
near Burnham, and the Rev. H. H. Crewe observed specimens near Drayton
Beauchamp, both in spring and autumn. Mr. A. H. Cocks informed Hartert,
in lift., that one was shot near Chequers Court about 1878, and another at Stoke
Mandeville " at least as long ago as 18S7." The Rev. Hubert Astley has several
times observed Ring-Ouzels amongst the juniper bushes near Wendover and
Chequers Court. In the Tring Museum is a (J shot at Wingrave 4 . xi . 1896,
while others have been observed in autumn, and two shot near Tring, September
14, 1893. Mr. E. E. Pettitt saw one on the Middlesex border, near Stanwell
Moor, on April 1, 1907 (in Hit.).
73 (164). BLACKBIRD. Turdus merula merula L.
B. of Berks, and Bucks, p. 14. Vict. Hist, of Bucks, p. 130.
Common resident.
Certainly one of the commonest birds in the county, and a great nuisance to
the fruit grower, making the growing of strawberries almost impossible, unless
the beds are netted.
74 (167). GREENLAND WHEATEAR. Oenanthe oenanthe leucorrhoa (Gin.).
Passage migrant.
This not uncommon passage migrant passes probably through Buckingham-
shire in numbers, as there are in the Tring Museum three rather typical specimens
shot in the neighbourhood of Tring : (J 20 . iv . 1893, (J 12 . iv . 1894, <J juv. 28 . ix .
1896.
75 (166). WHEATEAR. Oenanthe oenanthe oenanthe (L.).
B. of Berks, and Bucks, p. 76. Vict. Hist, of Bucks, p. 130.
Summer resident.
Apparently less frequent than it used to be. Kennedy (I.e.) talks of it as
" extremely numerous in summer " near Eton, where " a few nests are taken on
the commons every year." The Rev. Hubert D. Astley found it regularly breeding
on the slopes of Coombe Hill, near Wendover, and on chalk lulls above Princes
Risborough, in the vicinity of Whiteleaf Cross. Arthur Goodson saw it in June
near Buckingham. It used to breed on the bare slopes to the north-east of Tring
Station (in Bucks), towards Ivinghoe Beacon, but has not bred there for at least
eight or ten years, nor on the hills near Halton, where it nested regularly some
twenty years ago. Mr. C. Oldham saw twice, in 1913 and 1916, old birds feeding
young just out of the nest on Beacon Hill, near Wendover. Otherwise he has
NOVITATES ZOOLOGICAE XXVII. 1920. 193
only observed Wheatears as passage migrants from the middle of March to the end
of April, and again by the end of August. In the spring they are often observed
near the Reservoirs, on passage, chiefly in April. On May 4, 1913, Oldham saw
a male on the banks of Wilstone Reservoir which flew into a chestnut tree ; this
is unusual, but Hartert has seen Wheatears sitting on bushes and fruit trees in
the oasis of El-Golea in the Sahara.
It is probable that a number of the passage migrants are Greenland Wheat-
ears.
76 (176). BRITISH STONECHAT. Saxicola torquatus hibernans (Hart.).
B. of Berks, and Bucks, p. 21. Vict. Hist, of Bucks, p. 130.
Local resident, but most birds leave their breeding-grounds in winter.
In the Dinton Hall MS. recorded as being shot November 15, 1774. Now
rather local, but one or more pairs nest on most of the commons, where gorse
(furze) abounds. Mr. Oldham observed a pair on Cholesbury Common through-
out the winter of 1917-18, where they mostly leave their nesting-grounds for the
winter. Stonechats, on the other hand, often frequent the rushy margins of the
Tring Reservoirs in winter, and Oldham observed a pair at Wilstone Reservoir
throughout the winter of 1909-10, and again through the winter of 1910-11.
Hartert saw them there two or three times in February and March, 1915 and
1917. A few pairs breed in the south of the county : Mr. E. E. Pettitt has noticed
two or three pairs at Burnham Beeches, and several pairs also breed near the
Stanwell Reservoirs.
77 (175). WHINCHAT. Saxicola rubetra rubetra (L.).
B. of Berks, and Bucks, p. 76. Vict. Hist, of Bucks, p. 130.
Summer resident.
Somewhat locally distributed, and rare or absent from the hills and drier
districts, but regularly breeding along the Thames Valley, though not in any
numbers, also by the Ouse, Chess, in the Vale of Aylesbury, and in the north of
the county.
(A supposed occurrence of this species in winter, recorded in the Field for
February 4, 1911, p. 230, is probably attributable to a hen Stonechat.)
78 (178). COMMON REDSTART. Phoenicurus phoenicurus phoenicurus (L).
B. of Berks, and Bucks, p. 75. Vict. Hist, of Bucks, p. 131.
Summer resident.
The Redstart is generally not rare, but appears to be scarce on the Chiltern
Hills and uncommon in the beech woods, though more frequent in the neighbour-
hood of rivers, on the River Ouse, near Newport Pagnell, Castlethorpe, on the
Chess and Thames, and breeds also in Stowe Park and Buckingham, near Ayles-
bury and Halton, Chequers Court, Burnham Beeches, Mentmore, Amersham,
and doubtless many other places.
13
194 Novitates Zoolooicae XXVII. 1920.
79 (179). BLACK REDSTART. Phoenicians ochrurus gibraltariensis (Gm.).
B. of Berks, and Bucks, p. 171.
Exceptional visitor.
Kennedy (I.e.) mentions a specimen observed near Cookham, in Berks., not
far from Bucks., but the evidence appears to be somewhat inconclusive. Mr.
A. H. Cocks reports one as seen near Wooburn on June 11, 1909, a remarkable
date for the appearance of this species. On November 6, 1915, however, Chas.
Oldham observed a female or male of the year on the embankment of the Wilstone
Reservoirs, a few hundred yards from the Bucks boundary. " At times the bird
sought for food like a Robin on the sward which tops the embankment, but it
fed mostly among the stones, and made frequent little sallies into the air to snatch
insects, rising sometimes five or six feet above the ground. Twice whilst I watched
it, visits were paid to an adjacent orchard, but the bird was back again in a
minute or two on the embankment, where it seemed to find the best hunting"
(Oldham, Brit. B. vol. ix. p. 185, 1915).
(A supposed case of breeding near Windsor, reported in the Zoologist, 1916,
p. 237, is probably attributable to the Redbreast, t.c. p. 421.)
80 (180). NIGHTINGALE. Luscinia megarhyncha megarhyncha Brehm.
B. of Berks, and Bucks, p. 81. Vict. Hist, of Bucks, p. 131.
Summer resident.
Generally absent from the hills and drier beech woods, but found in many
places in the low-lying fertile districts, in the neighbourhood of water.
They used to breed in the neighbourhood of the Reservoirs about twenty-
five and twenty years ago, but have disappeared from there.
As a rule this species is fairly well distributed in the Thames valley, and
locally common. In 1917 Mr. Pettitt found it very scarce.
J. Macmeikan reports the arrival of the Nightingale on March 29, 1874,
an extraordinarily early date, and barely credible (Field, April 22, 1876, p. 464).
81 (185). BRITISH ROBIN. Erithacus rubecula melophilus Hart.
B. of Berks, and Bucks, p. 18. Vict. Hist, of Bucks, p. 131.
Common resident.
We have never seen the continental Robin (E. rubecula rubecula) in the
county and have not observed any migration. Of the many unusual nesting-
sites that have been recorded, one of the most unusual ones — and not, we should
say, beneficial to the books — is that of a pair which nested till recently, year
after year, on bookshelves in a house near Amersham.
82 (188). BRITISH HEDGE-SPARROW. Prunella modularis occidentalis (Hart.).
B. of Berks, and Bucks, p. 17. Vict. Hist, of Bucks, p. 133.
Common resident.
Found in every suitable locality. A perfectly white specimen, which had
been noticed for eight months previously, was captured on its nest near Tring in
April 1848 (H. H. Crewe, Zool. 1848, p. 2143).
Novitates Zoolooioae XXVII. 1920. 195
83 (189). WREN. Troglodytes troglodytes troglodytes (L.).
B. of Berks, and Bucks, p. 49. Vict. Hist, of Bucks, p. 133.
Common resident.
Found everywhere in woods, parks, orchards, gardens, and hedgerows.
84 (193). DIPPER. Cinclus cinclus britatmicus Tschusi.
B. of Berks, and Bucks, p. 170. Vict. Hist, of Bucks, p. 133.
Exceptional visitor.
According to Yarrell it has occurred on the Colne near Wraysbury, on the
Bucks border. Goidd (B. of Great Britain, vol. ii. p. 41) says he has known of
a solitary individual that had been killed on the River Chess. The Rev. H. Harpur
Crewe observed one on the canal near Drayton Beauchamp (Kennedy, I.e.).
T. Marshall, in a note on the occurrence of the Dipper in Hants., says that
a Dipper frequented the upper waters of the River Wick, above High Wycombe,
for two or three months in the autumn of 1894" (Field, December 3, 1898,
p. 897).
As Bucks is not a county with rapidly running mountain streams, the Dipper
can never be anything else than an exceptional visitor, the River Chess alone
approaching the type of stream suited to it, and that only in a few places.
85 (195). SWALLOW. Hirundo rustica rustica L.
B. of Berks, and Bucks, p. 88. Vict. Hist, of Bucks, p. 135.
Common summer resident.
Usually arriving in April, but in 1915 four were observed on the Tring
Reservoirs from March 26 to 31. The present Lord Rothschild has recorded
the hatching of one or more white Swallows together with normally coloured
ones from 1891 to 1895, in Aylesbury, evidently the offspring of one pair (see
Novitates Zoolooicae, vol. i. p. 667, and vol. ii. p. 484).
86 (197). HOUSE-MARTIN. Delichon urbica urbica (L.)
B. of Berks, and Bucks, p. 90. Vict. Hist, of Bucks, p. 135.
Summer resident.
Common, though absent from many apparently suitable villages. Supposed
to diminish steadily, but numbers fluctuate — though rather fewer appear in some
years, more are seen again in subsequent years.
Does not, as a rule, arrive before April, but has been seen near Eton during
the last week of March. Mr. Alfred Heneage Cocks observed an extraordinary
number, he thought " about a million "(?), over the river and pool at Great Marlow,
about 4 to 5 p.m. on September 18, 1896, and several hundreds on October 7,
1889. An old bird and two young were seen by the same observer on November
13, 14, and 15, 1889; and one is recorded from Eton on November 20, 1869 (" R. S.,"
Field, November 27, 1869, p. 458). The Rev. H. Harpur Crewe saw a Martin
at Hartwell, near Aylesbury, on December 5, 1874 (Zool. 1878, p. 3833).
196 Novitates Zoologicaz XXTO, 1020.
S7 (198). SAND-MARTIN. Riparia riparia riparia (L.).
B. of Berks, and Bucks, p. 90. Vict. Hist, of Bucks, p. 136.
Summer resident.
Not rare ; always to be seen on the Tring Reservoirs in summer, though we
have not found their breeding-place anywhere near.
A white Sand-Martin is recorded by T. Marshall as having been shot on the
Thames, near Marlow Road, August 20, 1867 (Quart. Mag. High Wycombe Nat.
Hist. Soc. No. vi. p. 146).
88 (200). SWIFT. Apus apus apus (L.).
B. of Berks, and Bucks, p. 91. Vict. Hist, of Bucks, p. 139.
Summer resident.
Common everywhere. Swifts leave in bulk before the end of August, but
sometimes, though quite exceptionally, some are seen as late as October or even
November. It is sometimes suggested that these are migrants from Scandinavia,
but this must be erroneous, because the most northerly breeding birds leave
first for the south.
(For the last six years Swifts left the neighbourhood of Tring during the night
from the 8th to the 9th of August, in 1919 leaving young in some nests to die.)
89 (202). NIGHTJAR. Caprimulgus europaeus europaeus L.
B. of Berks, and Bucks, p. 92. Vict. Hist, of Bucks, p. 139.
Summer visitor.
In suitable places by no means rare. It was, according to Kennedy, common
in the woods near Beaconsfield, and is so still. It is also more or less regularly
found, in summer, near Buckingham, Newport Pagnell, Bletchley, Aylesbury,
Halton, Wendover, St. Leonards, Coombe Hill and Chequers Court, Princes
Risborough, Burnham Beeches, Marlow, and the Hambleden district, and on
the outskirts of Ashridge Park.
90 (206). HOOPOE. Upupa epops epops L.
B. of Berks, and Bucks, p. 179. Vict. Hist, of Bucks, p. 140.
Irregular spring and autumn visitor ; one breeding record.
On account of its conspicuous plumage this bird is generally shot soon after
its arrival, and our records of occurrences go back for a century and a half. The
Dinton Hall MS. has excellent figures of two birds with the following note
appended : " Hoop or Dung Bird. Shot by William Lee of Ford, 1760. The
vulgar in country esteem it a forerunner of some calamity. It visits these islands
frequently, but not at stated seasons, neither does it breed with us."
About 1828 one was shot near Eton Wick and brought to John Gould, being
one of the first birds preserved by him. Kennedy also mentions one shot at
Lacey Green in 1838 as being in the collection of the Rev. B. Burgess, who also
informed him of a fourth, killed at Aston Abbots in 1851.
One was seen by the Hon. G. F. Berkeley at West Wycombe in April 1859
!R. B. Body, Field, May 7, 1859, p. 364), while another was wounded and captured
alive at Burnham Gore, near Maidenhead, on May 3 (I. Ingatton, Field, loc. cit.).
Kennedy also mentions one caught at Eton about 1860 or 1861, which lived for
NOVITATES ZOOLOGICAE XXVII. 1920. 197
about two years in confinement and became very tame. A female was shot at
Stewkley on April 24, 1862 (H. J. Jones, Field, May 3, 1862, p. 387). Another,
killed about two miles from Buckingham in 1867, is recorded by Kennedy, who
also states that specimens have been captured " more recently " near Chesham,
but gives no date.
In 1888 one was shot, presumably in April, on the Chilterns near Wendover
(E. C. Odling, Field, April 14, 1888, p. 536) ; and in the following year W. Tomalin
records one shot at Lavender Park Farm on November 21 (Field, November 30,
1889, p. 777).
All the above records probably relate to birds on spring or autumn migration,
and no evidence of breeding in the county was forthcoming till 1916, when Mr.
C. E. J. Hannett, in a letter to the Selborne Magazine, 1916, p. 93, stated that
a pair had actually bred near Taplow in that year and had apparently reared
at least one young bird. They were repeatedly seen in early spring by Mr. and
Mrs. W. R. Duiistan, in a rather secluded garden, but were not disturbed and the
nest was not found. Towards the end of the third week in May a single young
bird was seen by Mr. Dunstan in company with its parents. It was actually
caught by him, and described as about the size and weight of a good-sized Thrush.
The birds disappeared shortly before June 25, but the two parents were again
seen on July 5.
91 (208). KINGFISHER. Alcedo atthis ispida L.
B. of Berks, and Bucks, p. 52. Vict. Hist, of Bucks, p. 140.
Resident.
The Kingfisher is still regularly to be found on most streams and reservoirs.
Though not particularly numerous, it is always to be seen on the Tring Reservoirs,
in Stowe Park, and commonly on the Thames. It must have once been quite
numerous, and would be commoner now if it were not so often shot without
object or reason. A. R. Cocks tells us (Zoologist, 1891, p. 154) that a bird-stuffer
at Great Marlow had nearly a hundred specimens to stuff in the year 1890.
92 (209). BRITISH GREEN WOODPECKER. Picus viridis pluvius Hart.*
B. of Berks, and Bucks, p. 43. Vict. Hist, of Bucks, p. 139.
Resident.
Not rare wherever there are sufficiently old trees for them to nest in, but
of course absent from treeless tracts. It seems, however, to become scarce on
the lower ground in the eastern part of the Thames Valley, though fairly numerous
in the beech woods of the western part.
93 (211). BRITISH GREAT SPOTTED WOODPECKER. Dryobates major anglicus
(Hart.).
B. of Berks, and Bucks, p. 44. Vict. Hist, of Bucks, p. 139.
Resident.
Apparently formerly more numerous than nowadays. Now very scarce
in the Chilterns and Mid-Bucks generally, but evidently less rare in South Bucks.
. * Recent examination of larger series by Witherby and Hartert make it very doubtful if this
race can be separated, and it may be necessary to abandon it and call the British Green Woodpecker
Picus viridis virescens Brehm, which appears to be the correct name of the Central European form,
" pinciorum" being preoccupied. — E. H.
198 N0T1TATES ZOOLOGICAE XXVII. 1920.
In North Bucks it has been noticed at Stowe Park and Castlethorpe. Mr. Pettitt
records it as breeding at Burnham.
[BLACK WOODPECKER. Dryocopus martius martius (L.).
Kennedy (B. of Berks and Bucks, p. 178) says: "In March 1867, while
walking under some elms in Ditton Park, I saw a great Black Woodpecker busily
engaged on one of the tallest trees within a short distance of me. I was suffi-
ciently near to identify the bird with certainty, and had an opportunity of
observing its movements for the space of half a minute, when it flew off with
an undulating flight to a considerable distance, and was seen no more."]
94 (212). BRITISH LESSER SPOTTED WOODPECKER. Dryobates minor
comminutus (Hart.).
B. of Berks, and Bucks, p. 44. Vict. Hist, of Bucks, p. 139.
Resident throughout the year.
Though nowhere actually numerous, probably occurring in most of our
larger parks, woods, and orchards.
95 (213). WRYNECK. Jynx torquilla torquilla L.
B. of Berks, and Bucks, p. 86. Vict. Hist, of Bucks, p. 139.
Summer visitor.
Regular summer visitor, but has recently decreased in number, at least in
eastern and southern Bucks. Grossman found it common near Farnham and
Burnham. A pure white specimen, a young bird of the year, was killed in
September 1877 in the grounds of Wendover Hall and brought to H. Harpur
Crewe on October 23. It is now in the Calke Abbey collection (Zool. 1878, p. 29).
Mr. C. Wolley-Dod reports the arrival of this species at Eton on April 2, 1876,
an early date (Field, April 8, 1876, p. 414), but " H. M. B." states that in 1911
it was heard at Eton on March 13 (Field, March 18, 1911, p. 538). Some
interesting notes on the nesting habits of the Wryneck, as observed at High
Wycombe by R. C. Priestley, will be found in Wild Life, vol. ix. p. 268.
96 (214). CUCKOO. Cuculus canorus canorus L.
B. of Berks, and Bucks, p. 87. Vict. Hist, of Bucks, p. 140.
Common summer visitor.
Cuckoos appear to be more or less common everywhere. Near the Tring
Reservoirs, where they seem to lay exclusively in the nests of the Common Reed-
Warblers, they are numerous.
In the Thames Valley the Reed-Warbler is also a common foster-parent.
Mr. E. E. Pettitt has met with eggs or young in the nests of the following species
in this district : Marsh-Warbler (two cases), Garden-Warbler (one), and Reed-
Bunting (two), in addition to the ordinary foster-parents. He also obtained
eleven eggs which were obviously the produce of a single female in one season
( Wild Life, vol. vi. pp. 56-60, 92-7).
NOVITATES ZOOLOGICAE XXVII. 1920. 199
[SNOWY OWL. Nyctea nyctea (L.).
In the Zoologist, 1916, p. 313, Mr. A. Heneage Cocks gives full details of a
Snowy Owl seen by him and others, on July 31, 1912, at Yewdon Manor, Hamble-
den. When first seen it was seated on a sycamore tree in a hedgerow, but took
wing, and after croaking hoarsely passed within 80 yards of the observer. On
August 2 it was again seen by Mr. L. Deane, and two or three days later by Mr.
Deane, sen., the bird passing within 8 or 10 yards of him. There seems to
be no doubt as to the identity of the bird, but the date points to the bird having
escaped from captivity. It is, however, worth noting that genuinely wild birds
have occasionally been met with in summer : e.g. one is recorded from Elgin on
June 18, 1917 {Scott. Naturalist, 1918, p. 274).]
97 (222). LITTLE OWL. Athene noctua mira With.
Athene noctua mira With., Brit. B. xiii. p. 283 (1920 — Holland, etc.).
Vict. Hist, of Bucks, p. 141.
Recently introduced, now common resident.
Since 1890 Little Owls have been captured and reported from various parts
of Bucks, and during the last eight or ten years have become quite common.
All these are probably the offspring of the Little Owls introduced into Northamp-
tonshire by the late Lord Lilford, from Holland. Lord Rothschild also released
a number in Tring Park, but they almost, if not altogether, disappeared, and it
is only recently that this species has become common in the neighbourhood of
Tring. In the south of the county it has now become plentiful, being perhaps
attracted by the suitable breeding-sites provided by the old willows near the river.
Among the earlier records of occurrences, which illustrate the gradual spread
of this species, may be mentioned the following : one at Turville, January 1894
(C. J. Barnett, Field, May 26, 1894, p. 735) ; one at Fingest (T. Marshall, Field,
January 30, 1897, p. 135) ; Bletchley, 1902 ; and Fulmer, November 20, 1911
(H. H. Vyse, Field, December 2, 1911, p. 1234).
98 (224). LONG-EARED OWL. Asio otus otus (L.).
B, of Berks, and Bucks, p. 5. Vict. Hist, of Bucks, p. 140.
Resident.
Not numerous, but breeds regularly in woods and large parks, as for example
in Burnham Beeches and Fulmer (Clark Kennedy) ; the Chiltern Hills, at Beacons-
field ; Ashridge Park (H. H. Crewe) ; and Mentmore Park. Sometimes congre-
gates in considerable numbers ; in a wood to the west of Tring, Rothschild and
Hartert saw probably not less than forty on one day in autumn, when Pheasant-
shooting.
99 (225). SHORT-EARED OWL. Asio flammeus nammeus (Pontopp.).
B. of Berks, and Bucks, p. 104. Vict. Hist, of Bucks, p. 140.
Autumn and winter visitor.
Though not rare, of irregular occurrence, being apparently absent in some
seasons, and not found every winter anywhere. Generally met with more
200 Novttates Zoolooicae XXVII. 1920.
frequently in the low-lying districts, such as the neighbourhood of Drayton
Beauchamp, Marsworth, Long Marston (near the Reservoirs), and chiefly in
October and November, but also in fields on the Chiltern Hills.
[SCOPS-OWL. Otus scops scops (L.).
B. of Berks, and Bucks, p. 166. Vict. Hist, of Bucks, p. 141.
A. and H. Matthews wrote in the Zoologist, 1849, p. 2596 : " A bird of this
species was shot by a farmer on the borders of Buckinghamshire, near Brill, in
the spring of 1833, and taken to Mr. Forrest, from whom we shortly afterwards
received information of its occurrence."]
100 (229). TAWNY OWL. Strix aluco sylvatica Shaw.*
B. of Berks, and Bucks, p. 10. Vict. History of Bucks, p. 141.
Common resident.
The Brown or Wood-Owl is common in woods, parks, and other suitable
places throughout the county. O. V. Aplin (Zoologist, 1884, p. 471) mentions
an extremely grey variety " with the white markings conspicuous and no trace
of rufous tawny,"' which was shot at Great Horwood, near Winslow, in July
1884. In Great Britain the rufous tawny is the prevailing phase, while on the
continent greyish specimens are commoner.
101 (227). BARN-OWL. Tyto alba alba (Scop.).
B. of Berks, and Bucks, p. 8. Vict. Hist, of Bucks, p. 140.
Not uncommon resident.
Though decidedly less numerous than the Tawny Owl, this species is by no
means uncommon in suitable localities. Clark Kennedy states that a nest found
in Burnham Beeches in 1865 contained the unusual number of nine eggs, while
on one occasion eleven eggs were found in a nest near Tring. Mr. Grossman found
a bird incubating one of its own eggs and two of the Stock-Dove at Newton
Blossomville in 1893.
102 (233). PEREGRINE FALCON. Falco peregrinus peregrinus Tunst.
B. of Berks, and Bucks, p. 162. Vict. Hist, of Bucks, p. 142.
Irregular straggler on jxissage and in winter.
It is somewhat remarkable that we have comparatively few records of this
species, when it is remembered that it occurs regularly every year in the neigh-
bouring counties of Oxfordshire and Berkshire, and possibly closer observation
may result in its recognition as an annual visitor.
The Rev. Bryant Burgess in 1846 saw one which had been shot in Liscombe
Park. Another was reported by James Britten as having been captured in the
sixties in Brickhill Wood, near Woburn (Clark Kennedy, I.e.).
* In the Handlist of Brit. Birds, p. 109, we have called the British Tawny Owl Strix aluco aluco,
but it must be separated from the continental form. It is smaller, wings $ 246-264 (?268),
$260-276, while North and Central European examples measure $ 265-293, $267-304 mm.
Moreover, the brownish- rufous coloration predominates, grey ones being comparatively rare, and the
greyest not so whitish grey as the greyest and lightest on the continent, where the rufous type is
very much rarer than the grey one. Cf. Vog. pal. Fauna, ii. pp. 102.1, 1025. — E. H.
NOVITATES ZOOLOQICAE XXVII. 1920. 201
Mr. A. H. Cocks (in litt. 1902) states on the authority of Mr. W. Rhodes that
one was killed " about thirty years ago " at Fawley, and adds that another was
trapped " recently " at the same place.
An adult Peregrine shot at Old Windsor and sent to Curtis for preservation
on November 5, 1879, may have been a trained bird (Zoologist. 1880, p. 70).
Mr. G. Tickner killed a tiercel while pigeon-shooting about New Year's Day,
1894 or 1895, at Collett Farm, between Aylesbury and Tring.
Mr. John Chapman shot a moulting male in nearly complete adult plumage
on October 4, 1897, at Folly Farm, near Long Marston, on the Bucks boundary.
One was brought to the Rev. H. D. Astley at Chequers Court in the autumn
of 1898, which had been found drowned in the small reservoir on Beacon Hill.
Another male in full plumage was killed by a keeper, Charles Double, on
October 10, 1905, at Folly Farm, near Long Marston ; and on April 17 of the same
year a male moulting into adult plumage was shot near Tring.
Mr. W. D. Mackenzie (Field, February 23, 1907, p. 307) states that in 1905
a female was trapped in Fawley Park, and that another was picked up dead at
the same place on February 5, 1907.
Mr 0. V. Aplin (Zoologist, 1911, p. 7) records a fine and unusually dark-
coloured Peregrine in first year's plumage, shot at or near Buckingham, November
7, 1910.
A beautiful old Falcon was shot at Wingrave, on February 8, 1913, only
about two miles from Folly Farm, from which place two specimens are recorded
above.
In 1917 a pair of Peregrines stayed so late at Fawley Court as to lead to the
impression that they were breeding in one of the old elms from 100 to 120 feet
high, though no actual proof was obtained. In 1919 Mr. W. D. Mackenzie also
noticed a pair on several occasions in April : both birds were seen on April 21.
These birds subsisted almost entirely on Woodpigeons.
103 (235). HOBBY. Falco subbuteo subbuteo L.
B. of Berks, and Bucks, p. 69. Vict. Hist, of Bucks, p. 142.
Formerly bred in Bucks, and ■probably does so even now, ihongh only occasionally
observed.
According to Kennedy a pair nested in a wood near Datchet in the summer
of 1861, but four of the young ones were shot at Thorney almost as soon as they
could fly ; only two, however, were actually seen by Kennedy, and it is not very
likely that four came from the same nest. The same author speaks also of speci-
mens observed in Langley Park and of its occurrence near Chesham.
An adult male and female were shot at Folly Farm, near Long Marston,
close to the Bucks boundary, on August 14 and 16, 1894, by Mr. J. Chapman,
and another adult male near Drayton Beauchamp, May 28, 1912, by W. H. Price.
These specimens are in the Tring Museum. The last occurrence suggests that
the bird might have nested not far away, if left alive ; and in the County Museum
at Aylesbury are specimens shot near Wootton Underwood, August 1, 1908, and
June 26, 1909.
Mr. T. Steele Elliott (Zool. 1913, p. 465) also records an adult bird as killed
at Lavendon on August 23, 1913.
202 Novitates Zoological XXVII. 1920.
104 (236). MERLIN. Falco columbarius aesalon Tunst.
B. of Berks, and Bucks, p. 102. Vict. Hist, of Bucks, p. 142.
Winter visitor, but rare.
(E. Curtis (Field, December 27, 1879, p. 853) records two young birds shot
near Windsor, in Berkshire.)
Mr. J. Chapman shot two adult males at Folly Farm, near Long Marston,
on the Bucks boundary, on November 14, 1895, and December 21, 1897, both
being now in the Tring Museum.
On November 21, 1909, Mr. A. H. Cocks records a Merlin striking a bird
(apparently a Starling) within a few yards of where he was standing, and carrying
off its prey with some difficulty. Another was also seen by him while Partridge-
shooting.
C. Oldham [in litt.) has the following two observations : " February 21,
1915. A Merlin stooped at a Goldfinch on the bank of Weston Turville Reservoir."'
" February 25, 1917. An adult male observed near Wilstone Reservoir."
105 (237). KESTREL. Falco rinnunculus hiinunculus L.
B. of Berks, and Bucks, p. 1. Vict. Hist, of Bucks, p. 142.
Resident.
More in evidence in autumn and winter, but nesting wherever not destroyed
by keepers, who, if not energetically checked, kill every " hawk " — and owl !
| RED-FOOTED FALCON. Falco vespertinus vespertinus L.
B. of Berks, and Bucks, p. 102. Vict. Hist, of Bucks, p. 142.
Exceptional vagrant — one reported occurrence.
Kennedy (I.e.) gives the following somewhat unsatisfactory report: "The
inspector of the Eton police force — an intelligent man, who has a taste for natural
history — informed me that an Orange-legged Hobby was shot by the under-keeper
on Sir Harry Verney's estate at Steeple Claydon, near Buckingham, in January
1858. The date is an unusual one at which to find the species here, but my
informant is acquainted with the bird and is not likeiy to have been mistaken."]
[? GOLDEN EAGLE. Aquila chrysaetus chrysaetus (L.).
B. of Berks, and Bucks, p. 154.
Clark Kennedy (I.e.) mentions a Golden Eagle killed at Billing Bear, near
Cookham, in Berkshire, but not far from the Buckinghamshire border. Date
and year are not stated, but it was trapped by a keeper and its identification rests
on the evidence of Briggs, who collected many birds for Mrs. De Vitre. There
is no reason to believe that this specimen was ever seen by R. B. Sharpe (cf.
Quart. Mag. High Wycombe Nat. Hist. Soc. 1867, p. 123). Probably the date
was not later than about 1850. Another so-called "Golden Eagle," recorded by
Kennedy from Berkshire is known to be a White-tailed Eagle, and this may
well have been the case also in the present instance.]
Novitates Zooloqicae XXVII. 1920. 103
106 (242). ROUGH-LEGGED BUZZARD. Buteo lagopus lagopus (Briinn.).
B. of Berks, and Bucks, p. 165. Vict. Hist, of Bucks, p. 141.
Irregular and rare winter visitor.
Kennedy (I.e.) mentions a pair shot in Bledlow Woods, not far from Princes
Risborough, in November 1839. A specimen was trapped near Wycombe,
December 6, 1880 (T. Marshall, Field, December 18, 1880, vol. ii. p. 905). Mr.
Heatley Noble saw one at Fawley Court in the winter of 1885 or 1886. Three
were trapped (one alive) in the late autumn of 1891 near Halton, two of which
are preserved in the Tring Museum. In the autumn of 1912 Hartert saw one
alive in the possession of Mr. Harry Jenney, which had been winged by his keeper
not far from Aston Clinton. It lived for several weeks and then died.
Probably a " huge hawk " seen by a keeper near the Reservoirs in the winter
of 1917 was a Buzzard, and perhaps a Rough-leg.
107 (243V BUZZARD. Buteo buteo buteo (L).
B. of Berks, and Bucks, p. 104. Vict. Hist, of Bucks. vo\. i. p. 141.
Formerly a resident, now only a very rare straggler.
Although Buzzards probably bred at one time in most of our large woods,
our information on this point is lamentably scanty, though fortunately we possess
full details of what may have been the last nest in the county. Dr. Lamb, of
Newbury, writing in the early part of the nineteenth century (circa 1814), de-
scribed it as " very common " about that time in the neighbouring county of
Berkshire.* Its disappearance must have been very rapid, for Clark Kennedy,
writing in 1868, only gives three instances of its occurrence in the two counties
and Sharpe, in his articles on the " Birds of Cookham " (October 1867), refers
to one of these cases only.
Mr. T. Marshal], in a note contributed to the Quarterly Magazine of the High
Wycombe Nat. Hist. Soc. for January 1869 (p. 71), states that he has recently
received a long and interesting account of the taking of a Buzzard's nest in Bucks.
In 1806 Mr. R. Spicer, of Marlow, was a pupil of the Rev. Thomas Scott at Gaw-
cott, near Buckingham, and while shooting in the neighbourhood with two fellow-
pupils discovered a Buzzard's nest in the top of a high oak tree. " The tree was
of great size, and the nest was built on a fork which towered some 5 feet above
the rest of the tree. His companions tried, but in vain, to reach the nest. My
informant then essayed to do so, and after labours which nearly exhausted him,
succeeded in gaining the summit, and to his great joy found two eggs, very round,
large and thick, white with yellow spots." The eggs were taken and the descent
made in safety.
In 1874 one was killed at Little Marlow, which, according to Mr. T. Marshall,
had been observed and stalked for a long time previously. Another was trapped
near High Wycombe early in March 1875 (T. Marshall, Field, March 30, 1875,
p. 272).
One was seen on the wing at Hambleden on May 18, 1900, by Mr. A. H. Cocks,
who reports that a Buzzard (possibly the same bird) was killed at Datchet in the
following June (Zool. 1904, p. 34).
* Zool. 1880, p. 314.
204 NOVITATES ZOOLOGICAE XXVII. 1920.
Mr. E. M. Dowson saw one circling at 300-400 feet above the golf course at
Stoke Poges on April 13, 1913 {Field, April 19, 1913, p. 772).
108 (245). MARSH-HARRIER. Circus aeruginosus aeruginosus (L.).
B. of Berks, and Bucks, p. 4. Vict. Hist, of Bucks, p. 141.
Said to have been resident in former times ; no recent data.
Kennedy (I.e.) wrote : " Resident throughout the year, but nowhere numer-
ous. It is distributed sparingly in both counties, and is doubtless often con-
founded with the Hen-Harrier. It was formerly more common than it now is ;
and when there was a greater extent of uncultivated heaths and moorland wastes
the Marsh-Harrier might frequently have been observed sailing in mid-air in search
of prey. A few are still to be seen at various seasons in the neighbourhood of
Chesham ; and it remains all the year in some favoured localities, which are now,
alas ! ' few and far between,' in the two counties. The Rev. Bryant Burgess,
of Latimer, near Chesham, wrote me word of an immature Marsh-Harrier, which
was killed some years ago at Risborough."
Unfortunatety all these statements are rather vague and do not contain
one single exact date. The next record is fortunately more precise. Mr. A. H.
Cocks received a male alive, which had been winged near Spade Oak, Little
Marlow, in the heavy snow of January 19, 1881. This bird was kept for several
months in a walled-in garden, but was eventually killed by a Common Buzzard
on May 30, 1882.
109 (246). MONTAGU'S HARRIER. Circus pygargus (L.).
B. of Berks, and Bucks, p. 166. Vict. Hist, of Bucks, p. 141.
Occurring occasionally.
Clark Kennedy wrote [I.e.) : "The Rev. Harpur Crewe informed me that
a specimen of this bird was killed some years since by Mr. A. H. Jenney in the
parish of Drayton Beauchamp, in Buckinghamshire. It is now in the collection
of Sir J. H. Crewe. Mr. R. B. Sharpe sent me word that a Harrier of this species
was procured by a gentleman of his acquaintance near Eton in the summer of
1867, and is now in his collection."
Mr. A. H. Cocks [Field, February 8, 1873) records a specimen killed near
Hurley in 1870.
An adult male was trapped by a keeper near Wigginton, near Tring, close
to the border of Bucks, in the spring of 1891, and is in the Tring Museum.
110 (247). HEN-HARRIER. Circus cyaneus cyaneus (L.).
B. of Berks, and Bucks, p. 4. Vict. Hist, of Bucks, p. 141.
Formerly said to have been common, now disappeared.
Kennedy (I.e.) says that in the forties of the nineteenth century it was,
according to Mrs. Hussey, " a common bird in Buckinghamshire." A male
was shot at Eton College in 1857. A specimen shot in the Rev. H. H. Crewe's
time near the reservoirs is in the collection of Sir Vauncey Crewe. Another is
said to have been shot at the same place in December 1884. Kennedy also says,
Nqvitates Zoologicae XXVII. 1920. 205
" The Hen-Harrier has occurred at Chesham and near Cookham, and it has been
seen flying over Langley Park at such a low altitude as to enable the beholder to
ascertain the species.'' Unfortunately he gives no dates for these occurrences.
The latest occurrence of this species is that of a female bird, shot by a keeper
at Upton Wood, Langley, on October 23, 1911, and recorded by H. H. Vyse in
the Field for December 2, 1911, p. 1234.
Ill (248). GOSHAWK. Accipiter gentilis gentilis (L.).
Vict. Hist, of Bucks, p. 142.
Two occurrences only.
A male shot September 10, 1789, near Dinton Hall, by the Rev. W. Goodall,
is well figured in the Dinton Hall MS.
In the Quart. Jov.rn. of the High Wycombe Nat. Hist. Soc. vol. ii. p. 15, a
specimen of the Goshawk is recorded as having been exhibited at the third winter
session of the Society, which had been shot near Stone.
112 (249). SPARROW-HAWK. Accipiter nisus nisus (L.).
B. of Berks, and Bucks, p. 3. Vict. Hist, of Bucks, p. 142.
Resident.
Breeds in larger woods in spite of persecution by keepers. In winter in
parks and gardens, and working along uncut hedges.
113 (250). RED KITE. Milvus milvus milvus (L.).
B. of Berks, and Bucks, p. 163. Vict. Hist, of Bucks, p. 142.
Rare straggler, formerly resident.
There is no doubt that this species, like the Buzzard, formerly bred in the
larger woods of the county, and evidence of this is furnished by the prevalence
of local names such as " Kite's Wood,"' " Kite's Hill," especially in the Vale of
Aylesbury, as pointed out by John Young (Zool. 1892, p. 232). The same writer
also states that an old gardener named Lloyd used to tell stories of the depreda-
tions of the old birds, and of nests found in the neighbourhood of Quainton.
The references to socks and small linen found in the nest show that in this case
there was no confusion with the Buzzard.
The late S. VV. Jenney shot a Kite near the Wilstone Reservoir in the sixties,
which is now in the collection of Sir Vauncey H. Crewe. C. Wolley saw a Kite
in a field near Eton " many years ago " (Kennedy, I. c).
During the eighties one was reported to Mr. A. H. Cocks as frequenting
the late Mr. J. P. Ellames's property at Little Marlow, but though seen on several
occasions, managed to escape the usual fate of such visitors.
Mr. Guy C. Robson informed the present Lord Rothschild that on December
15, 1913, he twice saw a bird between Wendover and Halton which he felt sure
was a Kite, and independent enquiries tended to confirm the identification.
Kites were also identified in December 1913 in North Somerset, and from April
to June 1913 in Derbyshire (cf. Brit. Birds, vol. vii. p. 299).
206 NOVITATES ZoOLOQICAE XXVII. 1920.
114 (252). HONEY-BUZZARD. Pernis apivorus apivorus L.
B. of Berks, and Bucks, p. 165. Vict, Hist, of Bucks, p. 142.
Norv only rare casual visitor on migration.
Apparently this species formerly bred in the county, but as a nesting-species
it has long been extinct, though it is possible that an occasional bird may
still visit us, especially on the autumn migration from Scandinavia.
In an article on the " Pern or Honey Buzzard," by Edward Blyth, in Charles-
worth's Mag. of Nat. Hist. vol. i. p. 529 (1837), it is stated on John Gould's
authority that this species " breeds annually " at Burnham Beeches. The assertion
is repeated in A. G. More's paper in the Ibis, 1865, p. 13, " On the Distribution
of Birds in Great Britain during the Nesting-season."
Bryant Burgess informed Clark Kennedy of one which was captured in 1842
between Chesham and Missenden.
J. Gardner recorded one shot near Maidenhead in July 1867 (Field, July 27,
1867, p. 73). This is, however, almost certainly a Berks, record, as Mr. W. J.
Robson states (tn lift, to Mr. H. Noble, September 20, 1904) that a fine specimen
exists at Attwood which was shot at Shottsbrook [Berks.] about 1866. This is
evidently the bird set up and recorded by Gardner.
Two were killed in Shabbington Woods, near Brill, on or about September
23, 1882, by Mr. Henley's head- keeper, and one, a very dark bird, was set up by
Darby of Oxford (F. C. Aplin, Zoologist, 1882, p. 116).
115 (244). WHITE-TAILED, or SEA- EAGLE. Haliaeetus albicilla (L.).
B. of Berks, and Bucks, p. 155. Vict. Hist, of Bucks, p. 142.
Rare and irregular visitor in autumn or winter.
The earliest definite record of this species is contained in a paper on " The
Birds of Oxfordshire," by the Rev. A. and H. Matthews (Zool. 1849, p. 2594),
where it is stated that a White-tailed Eagle was caught in a trap near Chequers
Court in 1846. The Rev. H. G. Nind, of South Stoke, Oxon, also has a stuffed
specimen, formerly in his father's collection, which was killed on the playing-
fields of Eton about 1846, by the Rev. Edward Coleridge, then an assistant master
there (E. E. Pettitt in litt.). Another is also said by Messrs. Matthews to have
occurred " a few years ago " near Henley-on-Thames. Possibly this is the same
bird that Yarrell recorded, without further details, as having been taken at
Fawley Court, which is near Henley. C. E. Stubbs, when compiling his MS.
"Sketch of the Ornithology of Henley-on-Thames about 1868," also states
that " many years ago " a white-tailed Eagle was taken alive in a fir plantation
at Fawley Court. Probably the actual date was somewhere in the early forties.
(Cf. Zool. 1903, p. 445.) Kennedy mentions three or four occurrences from the
Windsor district in 1851, 1856, and 1865, but all apparently from the Berks, side.
An immature bird remained for some weeks in Fawley Court Deer Park
during the shooting-season of 1894-5, under Mr. W. D. Mackenzie's protection.
On one occasion he saw the Eagle settle in a tree just overhead. It was also seen
by Mr. H. Noble (Zool. 1903, p. 13). Probably this is the same bird which is
stated in the Vict. Hist, of Bucks., loc. cit., to have frequented Fawley Deer Park
"about 1885 or 1886."
NOVITATES ZOOLOGICAE XXVII. 1920. 207
116 (253). OSPREY. Pandion haliaetus haliaetus (L.).
B. of Berks, and Bucks, p. 158. Vict. Hist, of Bucks, p. 143.
Formerly the Osprey appears to have been an occasional visitor on migration
tn the reservoirs and the Thames Valley, but there are no records si?ice 1901.
The earliest occurrence of which we have any note is that of one killed in
February 1845 at Chequers, which is stated by Clark Kennedy to have passed
into the collection of Lady Frankland Russell.
In 1853, according to the Rev. H. Harpur Crewe (or 1854 as quoted by Clark
Kennedy), another was shot by a labourer on the bank of the canal at Halton,
while devouring a dead pigeon which was lying on the towing-path, and passed
into the possession of Sir Anthony de Rothschild, of Aston Clinton (Zool. 1865,
p. 9416 ; Ibis, 1865, p. 114). One which was shot at Hambleden in the winter
of 1858 had been seen for several days previously in the Fawley woods, according
to Mr. Dalziel Mackenzie.
One which had been seen fishing on the Thames for some days previously
was shot by the lodge keeper at Ditton Park on September 24, 1862 (T. Willis,
Field, October 4, 1862, p. 319). The date is erroneously given by Clark Kennedy
as September 26, 1863. Throughout the greater part of September 1864 two
Ospreys frequented the Wilstone Reservoirs. They were very tame, and were
apparently not molested by the keepers, but on September 30 the female was
killed, while eating a fish, by a country lad. The skin was afterwards given to
Mr. Harpur Crewe. The male left the neighbourhood shortly after, but John
Gould informed Mr. Crewe that another, also a male, was killed on the Thames
near Maidenhead about this time, which was probably the same bird {Zool.
1865, p. 9415 ; Ibis, 1865, p. 113). On May 9 James Street observed an Osprey
at the Tring Reservoirs. R. B. Sharpe gives details of another, which had been
seen near Hedsor for several days, and was finally shot on the Thames at Cookham
on October 6, 1864. He also refers to another which is said to have been seen
near the same place three days later, and was reported to have been killed at
Windsor (Quart. Mag. High Wycombe Nat. Hist. Soc. 1867, p. 124).
Clark Kennedy states that an Osprey was frequently observed on the Thames
near Surley Hall in 1865, 1866, 1867, and the early part of 1868, but though
frequently shot at, it managed to escape (B. of B. and B. p. 161). A female
was, however, shot by Captain Robson near Maidenhead in August 1867 ( Vict.
Hist. p. 143). L. Hibbert records another shot at Chalfont Park, near Slough,
on September 28, 1883 (Field, October 6, 1883, p. 490), which had been there for
about a fortnight previously. The last instance took place in 1901, when Mr.
Pope, jun., shot one on Aston Hill, above Halton, on October II. Reports from
two different sources would seem to indicate that a second bird was present in
the neighbourhood.
117 (256). WHITE STORK. Ciconia ciconia ciconia (L.).
B. of Berks, and Bucks, p. 189. Vict. Hist, of Bucks, p. 143.
Once recorded.
According to James Dalton, of Oxford, a stork was shot a few miles from
Buckingham, in September 1846 (Morris, Hist. Brit. B. vol. iv. p. 162, ed. ii.
1870).
20g NOVITATES ZOOLOQICAE XXVII. 1920.
118 (259). GLOSSY IBIS. Plegadis falcinellus falcinellus (L.).
Once recorded.
A Glossy Ibis, a bird of the year, was shot by a lock-keeper on the Wendover
arm of the canal, not far from Halton, in October 1886, and is now in the Tring
Museum (Littleboy, from Rothschild, in Hit., Trans. Herts. Nat. Hist. Sue.
vol. v. p. 82).
119 (260). COMMON HERON. Ardea cinerea cinerea L.
B. of Berks, and Bucks, p. 60. Vict. Hist, of Bucks, p. 143.
Resident, breeding in two or three localities, and -present on the reservoirs and
rivers throughout the year.
Herons are always to be seen on the Thames, Ouse, and the reservoirs, but
principally in late summer and autumn. On the Tring reservoirs it is no uncom-
mon sight to see a dozen or more together.
Probably the oldest heronry in the county is that which still exists, though
in greatly reduced numbers, at Harleyford Manor, above Marlow, on the
Thames. In 1866 C. E. Stubbs stated that there were over forty nests here, but
in 1 902 Mr. A. F. Grossman found that this once flourishing colony had dwindled
down to a few nests in two or three tall fir trees, and of late years the birds are
said to have been much disturbed by timber felling. At Fawley Court there is
now a flourishing colony, which in 1919 contained forty-four nests. Mr. W. D.
Mackenzie has supplied us with some interesting notes on the history of this
heronry, which is of comparatively recent origin. The first nest was built in an
oak, some time in the sixties, but the young birds were taken. In 1890 there
were two nests, four in 1891, and ten in 1892. About this time Mr. Mackenzie
saw no fewer than sixty-four birds on the wing at once. They had evidently
just arrived, and about half the number remained to breed, some sixteen nests
being built that year. Up to 1910 the number of breeding pairs varied from
eleven to sixteen, but from 1917 to 1918 it has remained stationary at about
thirty. The Rooks at Fawley Court have forsaken their old haunts near the house
and have followed the Herons to a wood about a mile away.
Another heronry is said to have existed in Claydon Park, but we can find no
direct evidence of this, and probably the statement is due to confusion of Claydon
Park with Harleyford Manor, which belonged to Lady Clayton.
About 1912 or 1913 a pair nested at Dinton on Colonel Goodall's property,
but the site appears to have been deserted. Mr. Edwin Hollis discovered a small
heronry of about a dozen nests near Gayhurst, about half a mile from the River
Ouse, in March 1919 (E. Hollis in litt.).
120 (266). NIGHT-HERON. Nycticorax nycticorax nycticorax (L. ).
B. of Berks, and Bucks, p. 189. Vict. Hist, of Bucks, p. 143.
Exceptional visitor.
According to Pennant (in litt. to Latham) an immature example (called the
" Gardenian Heron ") was shot near Cliefden in Bucks in 1797.
(Another immature example was killed near Thame, in Oxfordshire, not far
from Buckinghamshire.)
Sir H. Rae Reid (Field, August 26, 1899, p. 394) records the appearance
NOVITATES ZOOLOGICAE XXVII. 1920. 209
of one of these birds at Taplow for three or four days in August 1899, but there
is some r;ason to believe that this may have been an escaped bird.
121 (267). LITTLE BITTERN. Lrobrychus minutus minutus (L.).
B. of Berks, and Bucks, p. 186. Vict. Hist, of Bucks, p. 143.
Rare visitor, chiefly to the Thames Valley.
Clark Kennedy refers to several occurrences of this species on the Thames,
but in most cases with somewhat scanty data. An immature bird, shot on the
Thames near Windsor in the summer of 1826, was believed to have been bred in
the neighbourhood (cf. Yarrell, ed. iv. vol. iv. p. 202, and Zool. Journal, 1827,
p. 88). John Gould received another about 1828 from the Thames near Monkey
Island, and a third was shot on Queen"s Eyot, near Windsor, in the summer
of 1860. About 1856 or 1858 another was killed near Monkey Island, and others
of which no dates are given, are said to have been obtained near Surley, Windsor
and Uxbridge (Clark Kennedy, I.e.).
T. Marshall (Field, October 7, 1865, p. 254) recorded a specimen shot in
August 1865 on the Thames near Maidenhead.
Mr. A. Allen records a male bird killed near Olney " a few weeks ago " in
the Field, August 19, 1911, p. 474.
122 (268). BITTERN. Botaurus stellaris stellaris (L.).
B. of Berks, and Bucks, p. 187. Vict. Hist, of Bucks, p. 143.
Formerly breeding, now only an irregular and uncommon winter visitor.
A nest was found on one of the Tring Reservoirs (the great Marsworth
Reservoir) in 1849. The old bird was killed on the nest (!) and some of the eggs
were taken. One of these is in the Newton Collection in Cambridge, another
in that of Miss Ellen Williams, Tring.
Kennedy (I.e.) records a specimen shot at Fawley Court in January 1864,
one shot at Medmenham in 1851, and some killed near Chesham. One was shot
at Cockmarsh, close to the river, January 14, 1871 (Cocks, Field, 1873, p. 135).
The present Lord Rothschild shot one at the Reservoirs in 1890 or 1891. A male
was shot on Cholesbury Common 12 . xii . 1892 by William Street ; other speci-
mens were killed on the Tring Reservoirs 21 . xi . 1894 by James Street, 9 . ii . 1906
by the present Lord Rothschild, and 12. i. 1916 by James Street, three of
which were males. Another remained there for ten days, but left on
January 14, 1909 (Brit. Birds, vol. ii. p. 309).
In the winter of 1912 (probably in January, but date not recorded)
Rothschild observed a Bittern for ten minutes at Marsworth Reservoir.
Some years ago a Bittern stayed several weeks in winter at one of the
reservoirs, but no note was made of the date.
[An American Red Flamingo stayed several weeks on the reservoirs in the
summer of 1918.]
123 (271). WHOOPER SWAN. Cygnus cygnus (L.).
B. of Berks, and Bucks, p. 118. Vict. Hist, of Bucks, p. 144.
Rare winter visitor.
Kennedy (I.e.) quotes the following instances of the occurrence in Bucks.
In the winter of 1835 a Whooper was shot near Eton. Another was killed about
14
210 NOVITATES ZOOLOQICAE XXVII. 1920.
1837 near Eton, and two were shot above Surley Hall in 1838. " Some " were
procured in 1848 in the neighbourhood of Burnham, and two shot out of five
between Cookham and Maidenhead in 1855. In the winter of 1862 two were
killed at Wraysbury, and stuffed by Mr. Hasell, of Windsor. Another was
shot " on the river" in the winter of 1865-6. " Others have been brought at
various times to the Eton and Windsor bird-stuffers, but the dates of their
occurrence have been forgotten." Seven were seen for some days in some
meadows near Fawley and Greenlands during December 1860 and January 1861 ;
two were afterwards shot at Medmenham and one near Windsor. " This Swan
has been procured near Chesham." Some years before 1868 one was killed at
Latimer and was, in 1868, in the collection of Lord Chesham. On February 21,
1864, five " Wild Swans " were seen at Fawley, and with them were two Mute
Swans ; the two latter were lulled, but the Whoopers flew westward over the
( hiltern Hills. According to H. H. Crewe, the Whooper " occasionally visits
the reservoirs at Wilstone and Marsworth in severe winters."
In the winter of 1891 a flock of Swans visited the Tring Reservoirs ; two
were shot, of which one is a Bewick's, the other a Whooper. Another Whooper
was shot a week or two after.
124 (272). BEWICK'S SWAN. Cygnus bewickii bewickii Yarr.
Very rare winter visitor.
In the winter of 1891 a flock of Swans visited the Tring Reservoirs; two
were shot, of which one is a Bewick's, the other a Whooper. Both are in the
Tring Museum.
125 (273). MUTE SWAN. Cygnus olor (Gm.).
B. of Berks, and Bucks, p. G4. Vict. Hist, of Bucks, p. 144.
Semi-domesticated on many miters.
On the Thames and the Tring Reservoirs Mute Swans are living and propagat-
ing as if they were wild birds, and it is a wonderful sight to see them flying round
the reservoirs, and from one to the other of these waters, but the3r remain always
more or less tame, and never attain the shyness of wild birds.
126 (274). GREY LAG-GOOSE. Anser anser (L.).
B. of Berks, and Bucks, p. 199. Vict. Hist, of Bucks, p. 144.
Rare winter visitor.
According to Kennedy (I.e.), alighting sometimes on inundated meadows
in the Vale of Aylesbury, near Hulcott and Aston Clinton. The Hon. Walter
(now Lord) Rothschild informed Littleboy that a specimen was shot at the Tring
Reservoirs in September 1886. The late L. W. Wiglesworth told Hartert that
he had several times seen it on the River Ouse, near Castlethorpe.
127 (275). WHITE-FRONTED GOOSE. Anser albifxons (Scop.).
B. of Berks, and Bucks, p. 199. Vict. Hist, of Bucks, p. 114.
Rare winter visitor.
According to Kennedy (I.e.) it has occasionally been seen and shot on the
Thames (Eton, Datchet), and H. H. Crewe has observed it sometimes on the
reservoirs near Tring.
Novitates Zoolooicae XXVII. 1920. 211
" A White-fronted Goose with some Mallards in the rushes at Little Tring
Reservoir. It rose with the Mallards, and flew across to Wilstone Reservoirs,
but two hours later it was back at Little Tring, feeding in the rushes. When
disturbed it flew off, but returned presently and pitched on the water. This is
hardly the behaviour of a wild Goose" (C. Oldham in lift.).*
128 (277). BEAN-GOOSE. Anser fabalis fabalis (Lath.).
B. of Berks, and Bucks, p. 117. Vict. Hist, of Bucks, p. 144.
Rare visitor.
According to Kennedy (I.e.), visits the Thames from time to time, and has
been shot near Slapton and Chesham.
(From time to time — according to farmers and keepers now much more
rarely — geese are seen flying overhead, which may belong to this species, but
they are never identified.)
129 (283). BRENT-GOOSE. Branta bernicla bernicla (L.).
B. of Berks, and Bucks, p. 118. Vict. Hist, of Bucks, p. 144.
Rare winter visitor.
In 1865 a pair were shot near Datchet : one was killed on the Thames near
Eton and another near Cookham during the hard winter of 1866-7 ; the late
Rev. H. Harpur Crewe states that small flocks visited the Wilstone Reservoir
in severe weather. Two were killed and several seen at Surley in January
1867 (C. Kennedy, I.e.)
December 7, 1913, Charles Oldham observed a Brent-Goose with two Sheld-
Ducks on Wilstone Reservoir. It got up twice, while he watched it, once alone
and once with the Sheld-Ducks, but it seemed loth to leave the water and dropped
again, well out in the middle.
130 (285). COMMON SHELD-DUCK. Tadorna tadorna (L.).
B. of Berks, and Bucks, p. 205. Vict. Hist, of Bucks, p. 144.
Occasional visitor in winter or spring to the reservoirs awl Thames Valley.
A male was shot in March 1780, near Dinton Hall, and is very well figured
in the Dinton Hall MS. The Rev. H. H. Crewe informed Clark Kennedy that
he had observed it several times in winter on the reservoirs near Tring. One
was observed by Rothschild here 8 . i . 1 888, and another shot 6 . xi . 1893. James
Street saw a third 10 . i . 1897, and a fourth was shot 12 . xii . 1899. Both birds
shot were young males, and are now in the Tring Museum. C. Oldham saw two
Sheld-Duck and a. Brent-Goose on Wilstone Reservoir 7 . xii . 1913, two birds on
19 . iv . 1914, one on 18 . iv . 1915, a very wild male 28 . iv . 1918, and another
12 . v . 1918, all at the same place.
To the south of the county and the Thames Valley it is a scarce casual winter
visitor. Clark Kennedy mentions one shot on the Thames near Cookham some
* Knowing how many Geese and foreign Ducks are kept in England on ponds in parks and gardens,
and considering that Canada-Geese have often visited the Tring Reservoirs, and that an American
Flamingo was observed there two years ago, occurrences of all sorts of uncommon water-fowl are
open to suspicion, and each case must be taken on its merits and judged by collateral circumstances.
212 NOVITATES ZOOLOOICAE XXVII. 1020.
years prior to 1868, and also states (on R. B. Sharpe's authority) that one was
seen near Cookham for several days during the winter of 1867-8.
E. Curtis records one killed at Surley Hall on the Thames (Field, vol. liv.
December 27, 1879, p. 853) ; and Mr. E. E. Pettitt informs us that on December
30, 1906, he saw seven fly from the Bucks side and settle on the Stanwell
Reservoir, within the Middlesex boundary (in litt.).
Although this species is principally a resident on our low-lying coasts and
estuaries, there seems no reason why the above records should not relate to
genuinely wild birds, but it is possible that some may be due to the presence
of escaped park birds.
[RUDDY SHELD-DUCK. Casarca ferruginea iPall.).
Vict. Hist, of Bucks, p. 144.
Though we do not for a moment doubt that the many occurrences of this
species in Great Britain and Ireland in 1892 and several other years are those
of genuine wild birds from abroad, we must be prepared for the occurrence of
escaped birds in England, and the two appearances in Bucks shoidd no doubt
be referred to such. In 1S92 (Zoologist, p. 359) Mr. H. H. Vyse states that ten
were bred at Stoke Park, near Slough, of which only two were caught and pinioned,
while the rest flew away, usually when frost and snow came.
" A specimen killed at Wootton Underwood in December 190S, in the Bucks
County Museum. Probably an escaped specimen " (Edwin Hollis in lit!.).
Mr. C. Oldham observed a male and female on the Tring Reservoirs, March
21, 1915, of which he says, " no doubt escaped birds."]
131 (287). MALLARD or WILD DUCK. Anas platyrhyncha platyrhyncha L.
B. of Berks, and Bucks, p. 122. Vict. Hist, of Bucks, p. 145.
Common resident.
Nests in all suitable localities in small numbers, but in great numbers on
the Tring and Halton Reservoirs, especially the former. From about 1890
numerous eggs were hatched under hens and the ducks were fed during the whole
year. This, in connection with intense protection from poachers and other
unwelcome visitors as well as the destruction of all " vermin," resulted in an
unnatural increase in the numbers of Wild Ducks, and regular battues were held,
hundreds being killed on single days. From 1915-16 to the present time no
eggs have been hatched under hens and no food could be given, the severe winter
of 1916-17 caused some losses, and no doubt they were more closely shot down
in the surrounding district, so that their numbers decreased considerably. While,
therefore, small numbers only were shot, the decrease of the over-population
of ducks of this kind was probably welcome to other species, and the reappearance
of the Teal, among others, may be due to this fact.
[GAD WALL. Anas strepera L.
B. of Berks, and Bucks, p. 121.
We have no definite record for Buckinghamshire, but the late Rev. H. H.
Crewe informed Clark Kennedy that the Gadwall " has occasionally been killed
on the reservoirs at Marsworth and Wilstone " in winter.]
Novitates Zoolooicae XXVII. 1920. 213
132 (289). TEAL. Anas crecca crecca L.
B. of Berks, and Bucks, p. 123. Vict. Hist, of Bucks, p. 145.
Resident in small numbers ; common autumn and winter visitor.
" In the summer of 1861 two nests of this species were discovered among some
moss and rank herbage growing by the side of a pond near Burnham " (Ken-
nedy, I.e.).
Both H. H. Crewe and James Williams stated in 1 868 that Teal then nested
in limited numbers near the Marsworth and Wilstone Reservoirs. Apparently
they continued to do so until 1887, when a nest with five eggs was found by James
Street under a willow stump, which is exhibited, together with the old birds, in
the series of groups of British Birds in the Natural History Museum. Since
then there has been no definite record of the nesting of Teal until 1918, when a
brood hatched off at Marsworth Reservoir on July 14 (James Street). In that
same year Hartert saw some Teal in June, Oldham observed half a dozen at
Little Tring Reservoir on July 6, and Hartert thirteen about the middle of
August. In 1919 they were also seen in spring and summer. The late Lionel
Wiglesworth found it breeding in small numbers near Castlethorpe.
The Teal is a common winter visitor to the reservoirs. According to Old-
ham's observations, the first migrants usually arrive in the last week in July
(25, 1919; 25, 1914; 25, 1915; August 6, 1917 and 1918). From then until
the end of March they are about the Tring and Halton Reservoirs in varying
numbers — on July 1, 1914, Oldham saw more than a hundred on Wilstone
Reservoir. He saw birds in pairs, " no doubt on passage," in some years about
the middle of April.
Teal are occasionally met with on the Thames in winter, especially during
hard frost, when the inland waters are frozen over, and at the time of spring and
autumn migration.
133 (292). GARGANEY. Anas querquedula L.
B. of Berks, and Bucks, p. 123. Vict. Hist, of Bucks, p. 145.
Rare visitor.
According to the late Rev. H. Harpur Crewe, the Garganey " has been
several times obtained on the reservoirs at Marsworth and Wilstone in cold
weather" (Kennedy, I.e.). At the end of March 1849 four males and four
females appeared on one of the reservoirs near Tring and remained for some days.
On March 24 the Rev. J. Williams, with two other guns, obtained seven out of
the eight shot.* Subsequently seven more appeared, but moved off on the
following night (Zool. 1849, p. 2421).
Miss Williams informed Littleboy (Trans. Herts. Nat. Hist. Soc. vol. v. p. 83)
in 1887 that it was " an occasional summer visitor."
A $ in partial eclipse, the only bird of this species ever observed by him
on the reservoirs, was seen by C. Oldham August 3, and again August 11, 1918.
* One of these was later examined by Rothschild, while in the possession of the late George
Pratt in Marsworth.
214 Novitates Zoolooicae XXVII. 1920,
134 (-293). WIGEON. Anas penelope L.
B. of Berks and Bucks, p. 124. Vict. Hist, of Bucks, p. 145.
Not uncommon winter visitor and passage migrant on rivers and reservoirs.
" The first Wigeon usually arrive at the reservoirs in October (only in 1916
I saw three on September 26), and from then until early April frequent the Tring
and Halton (Weston Turville) Reservoirs in varying numbers. On February
23, 1919, Oldham and Hartert saw a flock of twenty. Birds on passage occur
in later April and May, e.gf. J 16. v. 1909, 3 24. iv. 1910, two $6 12. v. 1912,
pair 13. iv. 1913" (C. Oldham in litt.). Said formerly to have been " very
plentiful " on the Tring Reservoirs, but in recent years to have occurred there-
in small parties only (Grossman, Trans. Herts. Nat. Hist. Soc. vol. x. p. 96, 1901).
[MANDARIN DUCK. Aix galericulata (L).
B. of Berks, and Bucks, p. 208.
The adult male shot by Briggs on the river near Cookham in May 1866
was, of course, an escaped bird.]
135 (296). PINTAIL. Anas acuta L.
B. of Berks, and Bucks, p. 122. Vict. Hist, of Bucks, p. 145.
Fairly regular but uncommon visitor.
Clark Kennedy states that a male was shot on a sheet of ice in Stoke Park in
the winter of 1863, while the female which was in its company escaped. The
Rev. H. H. Crewe informed Kennedy " that this species visited the reservoirs at
Marsworth, Wilstone, and Weston Turville every winter in considerable numbers."
This latter statement can hardly have been correct, as the Pintail is now known
to be rather irregular in its visits to the reservoirs. A male was shot February
14, 1892, a female on October 3 of the same year, also in December 1893,
though the last had apparently escaped from a pond near Tring. Another male
in full moult January 31, 1006. An adult male was shot November 20, 1907.
Mr. C. Oldham observed males on eight occasions, but females only once : —
14.iii . 1909. A cj with some Mallards at Startops End.
24. xi. 1909. A <J with Mallards on the ice at Marsworth Reservoir.
12. i. 1913. A rS with some Mallards on Little Tring Reservoir.
16. i. 1916. A J in a pack of Mallards on Wilstone Reservoir. It was still
there January 23, and January 31 there were three males together— no female.
1 .iv.1917. " Two Pintails flying at a great height over Wilstone Reservoirs.
They dropped somewhere in the neighbourhood of the other reservoirs, and later
I found them— both adult males— asleep on the margin of Little Tring Reservoir."
1 .xii. 1917. An adult male with Mallards on Wilstone Reservoir.
20.1.1918. An adult male with Mallards on Wilstone Reservoir. Several
in February 1919, on Wilstone Reservoir.
1 .ii. 1919. Two males and two females at Wilstone Reservoir.
136 (295). SHOVELER. Spatula clypeata clypeata (L.).
B. of Berks, and Bucks, p. 121. Vict. Hist, of Bucks, p. 145.
Resident in small numbers ; also regular autumn and winter visitor.
Near Dinton Hall a Shoveler was shot on September 10, 1774, and four were
NOTITATES ZOOLOGICAE XXVII. 1920. 215
seen, one of which was shot, on August 29, ,1800. The Rev. H. Harpur Crewe
regarded it as a regular, though never a common, winter visitor on the reservoirs.
Nowadays it is not rare in autumn and winter, and one, two, or three pairs
have bred every year there for some time — from at least 1905 or before. In
June 1918 Hartert came across a female leading eight ducklings along a ditch
to the Wilstone Reservoir. In August he counted fifteen on Little Tring
Reservoirs. During the last few years more pairs have nested.
Mr. C. Oldham sends the following notes :
" The first Shovelers usually arrive at the end of September or early in Octo-
ber, and from then until mid-April are nearly always to be seen at the Tring
and Weston Turville Reservoirs. In the winter 1914-15 the numbers were
greater than usual. On December 6, 1914, I counted fifty-one on Startops
End, and seventeen more at Wilstone; on January 24, 1915, I saw twenty-one
on Wilstone; and on January 18, 1914, there were twenty at Weston Turville."
Oldham also saw an old bird, August 23, 1908, others May 2 and 16, 1909,
June 21, 1913 (three males in eclipse), July 25, 1914.
It appears to be rarely met with on the Thames, but E. E. Pettitt saw a male
near Queen's Eyot, February 18, 1917 (in litt.).
137 (297). RED-CRESTED POCHARD. Netta rufina (Pall.).
Vict. Hist, of Bucks, p. 145.
Rare visitor ; some specimens probably escaped birds.
Littlcboy recorded a female shot on the Tring Reservoirs in September
1887, but the specimen was erroneously identified by Rothschild, it being only
an abnormally coloured female Scoter (Vict. Hist, of Bucks. I.e.). A flock of
about forty individuals, however, visited Wilstone Reservoir in the autumn of
1889 or 1890, out of which four males and two females were shot. Three males
and one female of these are now in the Tring Museum, and a pair in Mr. John
G. Millais' collection. The exact date is not preserved, the labels of the specimens
giving only the locality.
A beautiful male was shot on the reservoirs 9.xi.l915. On November 4,
1917, Charles Oldham observed an adult pair on Little Tring Reservoir. In
December 1918 a male was on Halton Reservoir for over a fortnight at least.
It was seen on several occasions by Oldham and Hartert.
As these beautiful birds have nested for several years in Woburn Park, this
last bird — and possibly others of the single birds recently seen — was probably
an escape ; it was by no means very wild. In January 1920 a male was recorded
on Halton Reservoir by the keeper.
138 (298). COMMON POCHARD. Nyroca ferina ferina (L.).
B. of Berks, and Bucks, p. 127. Vict. Hist, of Bucks, p. 145.
Not uncommon, but very load resident.
The Pochard has, like the Tufted Duck, spread and increased in many parts
of England, especially in the eastern counties. It probably nested in Bucks
long ago, as a specimen was shot at Dinton Hall on June 16, 1825. In 1868 it
was, however, not yet common, as Kennedy (I.e.) thought it still worth to record
single occurrences, and he was informed by the Rev. H. H. Crewe that the Pochard
216 Novitates Zoological XXVII. 1920.
had " on two occasions been known to breed on the water near Drayton Beau-
champ," a nest containing eggs having been taken in June 1850 at the Marsworth
Reservoir by a gamekeeper , of the Rev. James Williams, and a pair breeding
on the banks of the same piece of water " a few years later." At the same time
the late Rev. J. Williams, who had taken eggs at Wilstone Reservoir, believed
that it bred there " in limited numbers every year." Now the species breeds
numerously at the Halton and Tring Reservoirs. Their numbers seem to fluctuate
somewhat, and have, since 1915, decreased a little, probably only temporarily.
The Pochards that are killed during Duck-shoots are not very many.
To the Thames and the south of the county generally it is chiefly known as
an uncommon winter visitor in severe weather when the reservoirs are frozen.
Breeding is, however, known to have taken place at one locality in the south of
the county. Two pairs nested on a pond in the Burnham Beeches district in
1916, and it is quite possible that they may have nested there previously (E. E.
Pettitt. in lift.).
139. BAER'S DUCK. Nyroca nyroca baeri (Radde).
A male was shot, in the presence of the Hon. N. Charles Rothschild, on
Marsworth Reservoir, on November 5, 1901.
It is, of course, in many cases impossible to say whether a Duck shot in
England is of direct foreign origin, i.e. a wanderer from afar, or whether it has
escaped from ponds in parks where so many foreign ducks are now kept and bred
in semi-confinement. In this case, however, all enquiries tend to prove that this
specimen was a genuine migrant, though the first and only known occurrence in
Europe. The specimen was exhibited by the Hon. N. Charles Rothschild at the
B.O.C. meeting on November 20, 1901 (Bull. B.O. Club, vol. xii. p. 25). "The
exhibitor urged in support of the view that the specimen was a wild, rather than
an escaped bird : (a) that no specimen of this duck had escaped from the Zoolo-
gical Gardens, where there were now four pinioned examples sent by Mr. Frank
Finn, of Calcutta ; (6) that both the Duke of Bedford and Mr. J. G. Miilais had
stated, in reply to enquiries on the subject, that they were not aware of any of
these birds having been turned out on artificial waters in this country."
In Brit. B. vol. i. p. 14 (1907), Howard Saunders deprecated the admission
of Baer's Duck to the " British List," stating that it was " well known that the
species had been introduced on the ornamental waters of England." In the same
volume, p. 63, the Hon. Walter Rothschild replied, asking for further explanation
of the statement with regard to the introduction to ornamental waters. No
response, however, was forthcoming, and enquiries from dealers and owners of
" ornamental waters " did not elicit any new facts about the introduction of
Baer's Duck before or in 1901.
140 (300). TUFTED DUCK. Nyroca fuligula (L.).
,B. of Berks, and Bucks, p. 129. Vict. Hist, of Bucks, p. 146.
Now numerous resident on Weston Turville and Tring Reservoirs.
In 1868 this Duck was only known to Kennedy (I.e.), and Harpur Crewe as
a "common winter visitor" to the Tring Reservoirs. In 1893 it was already
nesting on these waters, and also on the Halton (Weston Turville) Reservoir,
Novitates Zoolooicai: XXVII. 1920. 217
but not in large numbers. Since then it has become much more numerous and
it is now a very common breeder.
To the Thames Valley and the Stanwell Reservoirs it is still only known at
present as a winter visitor, usually occurring on the river during severe frosts,
but occasionally met with at other times. Pettitt reports it as common at
Stanwell, and has observed it at Burnham, Horton, and Hambleden.
141 (301). SCAUP. Nyroca marila marila (L.).
B. of Berks, and Bucks, p. 129. Vict. Hist, of Bucks, p. 146.
Irregular winter visitor to the reservoirs.
" On the 26th of January, 1855, the Rev. B. Burgess observed a female Scaup
Duck swimming about in company with Coots and Dabchicks on the water in
the park at Latimer, near Chesham, which was not frozen, and a few days after-
wards Mr. Elliott, of Chesham Bois Mill, sent him a Scaup which he had just
shot on the stream. The Rev. H. Crewe states that it is an occasional winter
visitant to the Wilstone Reservoirs" (Kennedy, I.e.). G. A. Crewe records
four seen by him about three weeks previously on the Grand Junction Reservoir,
while staying at Drayton Beauchamp (Field, December 15, 1883, p. 809). One
was shot on the Tring Reservoirs in October 1884; and in December 1900 or
January 1901, Rothschild and Hartert observed a large flock.
The following specimens are now in the Tring Museum :
cJ juv., 2.xii.l892.
$, 7.xi.l905.
<J$, 20. xi. 1907.
?, 12. i. 1912.
cJ in nearly full plumage, 23. i. 1912.
?, 24. i. 1913.
Mr. Oldham made the following notes :
"27.x. 1907. $, Wilstone Reservoir.
" 1 8 . xii . 1 909. Adult <J, Wilstone Reservoir.
"21.1 .1912. Pair on Marsworth Reservoir. $ not in full plumage, mantle
only partially vermiculated and showing a good deal of brown, flanks dusky brown
as in the $. Street told me some months afterwards that he had shot the <J and
hit the $, but failed to drop her. On March 10 there was a $ — presumably this
bird — standing with some Pochards and Tufted Ducks on an island in Little
Tring Reservoir. She was there again on March 17, and, although she may
have been wounded, was able to fly well. I saw the bird again at the same place
on March 30, April 13, and April 21. I saw nothing of the bird after that until
July 21. On that date she was on Marsworth Reservoir with two ducklings —
sooty little things like young Tufteds. I have no doubt that the ducklings were
hers, for she was with them for an hour and a half while I watched them in the
morning, and again when I passed the place in the evening. There were many
young Tufteds on the water, but the Scaup was never many yards away from her
own two, and they went with her wherever she went in the corner of the reservoir
that constituted their feeding-ground. Once, when a Coot came near them, she
drove it away, and she made an angry rush at a Dabchick which approached
them. She even drove off a Tufted Duckling, of larger size than her own, when
it crossed their path. The Scaup had presumably paired with a Drake Tufted.
21 8 NOVITATES ZOOLOGICAE XXVII. 1920.
[No bird showing sign of hybridism was subsequently shot on the reservoirs.
— E. H.]
" 4.1.1914. Two white-faced birds, on Marsworth Reservoir.
" 15.iii. 1919. A female Scaup at Little Tring Reservoir."
142 (302). GOLDENEYE. Bucephala clangula clangula (L.).
B. of Berks, and Bucks, p. 130. Viet. Hist, of Bucks, p. 146.
Irregular winter visitor to larger waters.
In 1849 the Rev. J. Williams stated that small flocks visited the Tring Re-
servoirs annually, arriving at the end of October and staying till driven away
by frost, but that nearly all were females or birds of the year. He records one
fine male in full plumage shot early in 1849 (Zool. 1849, p. 2421).
The late Rev. H. Harpur Crewe also described the Goldeneye as a " regular
visitor " to the Tring Reservoirs, but its visits are now rather irregular, though
by no means rare. Rothschild and Hartert have often seen single birds and small
flocks, when shooting on the reservoirs, and the following specimens have been
shot and are now in the Tring Museum :
$, 26. i. 1893.
(J juv., still in almost complete juvenile plumage, 10. i. 1901.
$ad., 26.x. 1901.
?, 28.xii.1905.
$ad., 11. i. 1906.
$ ad., 10. xi. 1908.
cj ad. and $ ad., 13 .i . 1909, the <J in perfect plumage.
(J of the year in almost complete juvenile plumage, 4 . ii . 1914.
$ad., 6. u. 1914.
cJ ad. in full plumage, 7.1.1915.
<J with traces of eclipse plumage, 9.xi.l915.
$, 24.xii.1915.
<J juv., 1 .i. 1920.
Larger flocks than usual were seen by Hartert in December 1893 and
January 1894.
Mr. Oldham observed the following specimens :
1 .iii. 1908. An adult male and a brown-headed bird, Wilstone Reservoirs.
10. iv. 1910. An adult male and a female, Wilstone Reservoirs.
5.vii.l911. A brown-headed bird, Wilstone Reservoirs.
30. xi. 1913. A male assuming full plumage and two brown-headed birds,
Wilstone Reservoirs.
20.xii. 1914. An adult male and brown-headed bird on Wilstone, a brown-
headed bird Startops End Reservoir.
21. xi. 1915. A male in nearly full plumage, and three brown-headed birds
on Wilstone Reservoirs.
20. i. 1918. A brown-headed bird, Wilstone Reservoirs.
28. iv. 1918. A brown-headed bird, Wilstone — the latest date.
From 24. xi. 1918 until mid-January 1919, two and sometimes three
constantly on Wilstone Reservoirs.
15. iii. 1919, three on Wilstone Reservoirs.
Novitates Zoolooicae XXVII. 1920. 219
In February 1917, when the Reservoirs were frozen over and hundreds
of Ducks were crowded together on a small open space on Wilstone Reservoirs,
Hartert saw among them several adult males ; there were probably some females
as well, but without a telescope he could not make them out in the crowd of other
Ducks.
On January 8, 1919, Lord Rothschild saw two adult males and a brown-
headed bird on Wilstone Reservoir.
On the Thames it is usually met with in hard winters, such as 1916-17,
when it was not uncommon (Jourdain). Four were seen at Queen's Eyot on
February 2, 1917, by E. E. Pettitt.
143 (304). LONG-TAILED DUCK. Clangula hyemalis (L.).
Very rare winter visitor.
A young male was shot at one of the reservoirs 28 .x . 1892. An adult male
still retaining some feathers of the summer plumage on back and scapulars was
shot on the reservoirs 12. xi. 1906 ; a young male on Marsworth Reservoir 20. xi.
1908 (Br. Birds, vol. ii. p. 309), and another male in moult 2.xi.l915. All four
specimens are in the Tring Museum.
On November 8, 1908, C. Oldham observed a young bird on Wilstone
Reservoir, perhaps the same bird which was shot on Marsworth Reservoir on
the 20th.
[HARLEQUIN DUCK. Histrionicus histrionicus (L.).
B. of Berks, and Bucks, p. 206.
Clark Kennedy records one occurrence of this species on R. B. Sharpe's
authority as having been shot during the winter of 1866-7 on the river at Maiden-
head, and preserved by Wilmot, the bird-stuffer of that town. Sharpe does
not refer to this specimen in his Handbook of the Birds of Great Britain. Probably
a mistaken identification.]
144 (309). COMMON SCOTER. Oidemia nigra nigra (L.).
B. of Berks, and Bucks, p. 125. Vict. Hist, of Bucks, vol. i. p. 146.
Irregular and generally rare visitor to the Tring Reservoirs and the River
Thames.
Although chiefly a marine species, except during the nesting-season, the
Common .Scoter has occurred not infrequently on the Upper Thames. Clark
Kennedy mentions one shot in the winter of 1862 at Datchet, and another killed
in 1865 near Cookham. The latter was a male in adult plumage, and was also
killed in winter. E. Curtis (Field, March 29, 1879, p. 369) records a male seen
by him, which was shot on the Thames near Windsor on March 22.
On the Tring Reservoirs they are sometimes, though irregularly, observed.
A female was shot in October 1884.
In October and December 1892 there were quite a number on the reservoirs,
four females being preserved in the Tring Museum. A young male was shot at
Deadmere, Great Marlow, December 18, 1893, by Joe Cox, jun. (A. Heneage
Cocks in litt.).
On April 10, 1910, ten Scoters were observed by C. Oldham, Erwin Strese-
220 Novitates Zoolooicae XXVII. 1A20.
mann, and Ernst Hartert on Startops End Reservoir, seven of which were adult
males. Five more — three of them adult drakes — were on Wilstone Reservoir,
and eleven on Weston Turville Reservoir, of which seven were adult drakes.
After a long spell of N.E., E., and N. wind, on the 9th it had veered to N.W.
and on the 10th to a light S.W. breeze (C. Oldham, Brit. Birds, vol. iii. p. 414).
On July 13, 1913, C. Oldham saw a female or immature male on Wilstone
Reservoir, which was still there on July 19, on which day an adult male was seen
at Weston Turville (op. cit. vol. vii. p. 119). The date of these latter records
is remarkable.
An adult male on Startops End Reservoir on March 7, 1915 ( C Oldham in
lilt.). An adult <$ and an adult $ observed on Wilstone Reservoirs, April 29,
1917 (idem, in litl.). February 7, 1918: an adult male shot on Marsworth
Reservoir, preserved in the Tring Museum.
Mr. E. E. Pcttitt informs us that two shot at Bell Weir are now preserved
at the " Angler's Rest," Egham (in litt.).
145 (310). VELVET SCOTER. Oidemia rasca fcsca (L.).
B. of Berks, and Bucte. p. 206. Vict. Hist, of Bucks, p. 211.
Very exceptional visitor.
J. Gould (Birds of Great Britain, vol. v. pi. 29, text) states that " during
the severe winter of 1866-7 a splendid old male was killed at Cookham, in Berk-
shire." This specimen was almost certainly shot on the river, which forms the
boundary between the two counties.
The Rev. H. Harpur Crewe told Kennedy that he had on two occasions
observed the Velvet Scoter on the large reservoir near .Drayton Beauchamp in
cold weather, but he gave no dates or other particulars !
Mr. J. M. Knapp records one killed at Linford, Bucks, on October 27, 1890
(Field, November 1, 1890, p. 668).
146 (312). GOOSANDER. Mergus merganser merganser L.
B. of Berks, and Backs, p. 131. Viet. Hist, of Bucks, p. 146.
Irregular and uncommon winter visitor.
A female (called Mergus serrator, but from the figure a Goosander) was shot
at Dinton Hall on November 26, 1774. Kennedy mentions several specimens
obtained on the Thames in 1847, 1856, 1860, 1864, 1866, and 1867 (the last seen
only), and says that in hard weather it is " often found on the reservoirs near
Drayton Beauchamp." Mr. Heneage Cocks says (in litt.) that one was shot near
Great Marlow January 27, 1881. Two were killed at Tring in February 1885,
and two seen by the keeper on November 25, 1895, as well as two in January
1896 (Vict. Hist, of Herts, vol. i. p. 211). Single females were shot there by
James Street on November 8 and 29, 1901, and November 21, 1902.
A most interesting specimen, a male in eclipse plumage, was killed by Street,
August 31, 1903, and an adult male in full brilliant plumage was shot during a
Duck-shoot on December 1 1 of the same year.
Mr. Oldham observed two " brown- headed birds " (females) on Wilstone
Reservoirs February 27, 1910, another on December 18 of the same year, which
•' from the purity of its colours and small size he judged to be an adult female."
NOV1TATES ZOOLOGICAE XXVII. 1920. 221
January 21, 1917, he saw an adult male on Wilstone Reservoirs. A pair were
on the reservoirs during the last week of December 1919 until January 1, 1920.
147 (313). RED-BREASTED MERGANSER. Mergus serrator L.
B. of Berks, and Bucks, p. 131. Vict. Hist, of Bucks, p. 146.
Rare winter visitor.
The Rev. H. H. Crewe informed Clark Kennedy that small parties of four
or five were seen on Wilstone Reservoir almost annually. " A year or two before
1883, which was the first year I shot on the reservoirs, the Rev. A. Birch shot
a female on Little Tring Reservoir, which he had stuffed " (Walter Rothschild,
Vict. Hist, of Bucks, p. 146). Several visited Marsworth Reservoir in November
1901 ; on the 5th the Hon. N. Charles Rothschild shot a female, and on the 7th
James Street a male and a female ; all three are in the Tring Museum.
On the Thames it is of very rare occurrence, but a female is mentioned by
Clark Kennedy as having been shot at Wraysbury in the winter of 1854, and
another was reported by R. B. Sharpe from Cookham a few years prior to 1868.
148 (314). SMEW. Mergus albellus L.
B. of Berks, and Bucks, p. 207. Vict. Hist, of Bucks, p. 146.
Rare winter visitor.
The earliest record of this species from the county is that of a female shot
on November 23, 1774, at Dinton Hall. Now and then small flocks or single
birds — very rarely adult males — are observed on larger waters. In the winter
of 1850-51, however, an adult male was killed on the Thames near Boveney
Lock. In the winter of 1861-2 a flock of five was observed by Harpur Crewe
on the Wilstone Reservoirs, where they remained several days (Kennedy, I.e.).
Mr. A, Heneage Cocks records an adult male shot in January 1876 on the Thames,
opposite Stonehouse {Zool. 1891, p. 153). A flight of nine visited Marsworth
Reservoir about the middle of February 1885 (Littleboy, ex Rothschild, in lilt.,
Trans. Herts. Nat. Hist. Soc. vol. v. p. 83). A young female was shot on January
12, 1891, at the Brewery Sewage Works below Great Marlow (A. H. Cocks, Zool.
1891, p. 153).
On January 26, 1913, Oldham saw a single brown-headed bird on Little
Tring Reservoirs, another (or the same) on February 22, and again March 2 ;
while Lord Rothschild saw three, an adult male and two brown- headed ones,
on Wilstone Reservoir. On January 6, 1917, Oldham again saw a brown-headed
Smew on Wilstone Reservoirs, and again on January 20, evidently the same bird.
Another female was seen by Oldham in the same place on February 17, and again
March 3, while an adult female was shot there December 12, 1917, which had been
seen for nearly a fortnight.
149 (316). CORMORANT. Phalacrocorax carbo carbo (L.).
B. of Berks, and Bucks, p. 214. Vict. Hist, of Bucks, p. 143.
Rare occasional visitor to the Thames and reservoirs.
Clark Kennedy mentions one shot near Marlow Railway Bridge about 1857,
on R. B. Sharpe's authority, and another shot on the Weston Turville Reservoir
in 1858.
222 NOVITATES ZOOLOGICAE XXVII. 1020.
The late C. E. Stubbs, of Henley (ob. 1872) states in his Egg-Bpok, probably
completed about 1868, that he has known Cormorants shot in winter (among
other places) at Bolney, Magpie Eyot, Medmenham, and Marlow (cf. Zool. 1903,
p. 453).
On June 2 and August 8, 1900, James Street observed single birds on the
Tring Reservoirs, and on November 15, 1900, two specimens.
Mr. A. H. Cocks saw a Cormorant or Shag flying on the Thames between
Bisham and Marlow in a thick fog, but was unable to identify the species with
certainty. This was some time prior to 1902.
In 1902 an immature Cormorant was seen for some weeks on the Thames
near Culham Court, above the Bucks boundary ; and either this or a second bird
was subsequently seen on the river below Henley, according to Mr. C. Barnett
(H. Noble, MSS.).
On October 11, 1907, and April 29, 1909, young males were shot on the Tring
Reservoirs, both of which are now in the Tring Museum. On April 25, 1909,
Mr. C. Oldham saw a single bird on the reservoirs, doubtless the bird which was
shot there four days later, and also records others seen at the same place on
September 4, 1910, May 5, 1912, and July 25, 1914. Mr. Oliver Pike observed
a Cormorant on Wilstone Reservoir, September 14, 1919.
Mr. E. E. Pettitt informs us that there is a stuffed specimen at the " Bells
of Ousely," Old Windsor, which was shot on the river at Wraysbury " a few
winters ago."
150 (317). SHAG. Phalacrocorax graculus graculus (L.)
B. of Berks, and Bucks, p. 214.
Very rare visitor.
According to Kennedy (I.e.), a Shag was shot on the Thames near Wraysbury
in 1850. A bird of the year was shot on the reservoirs October 14, 1903, another
October 22, 1908 (Brit. B. vol. ii. p. 309), and a third January 16, 1917 ; all
three are in the Tring Museum.
Mr. Oldham (in litt.) observed a Shag, also a young bird, at Marsworth
Reservoir August 30 and September 7, 1913. In the Bucks County Museum
in Aylesbury is an immature bird killed on Oving Church, 20.xii.1909 (Edwin
Hoiks in litt.).
151 (318). GANNET. Sula bassana (L.).
B. of Berks, and Bucks, p. 216. Vict. Hist, of Bucks, p. 143.
Accidental visitor : three occurrences.
A Gannet was captured by the Rev. T. Rogers, at Sherrington, near Newport
Pagnell, in November 1847. Another was killed on the canal near Wendover
in 1886. In the Bucks County Museum, Aylesbury, is an adult male picked up
alive, 9.xii.l91d, by a labourer in a meadow in Hambleden parish and brought
to Mr. A. H. Cocks. Although apparently unable to move, no trace of injury
could be found (A. H. Cocks and E. Hollis in litt.).
NOVTTATES ZOOLOQICAE XXVII. 1920. 223
152 (319). STORM-PETREL. Hydrobates pelagicus (L).
B. of Berks, and Bucks, p. 218. Vict. Hist, of Bucks, p. 152.
Rare straggler ; jour or five occurrences.
F. 0. Morris states that a specimen was picked up dead near Buckingham
but does not give the date. Kennedy records the finding, during the last days of
October 1859, of a Storm- Petrel on the road opposite the Priory, Burnham, and
also mentions another which was shot in the neighbourhood of Burnham in 1865,
while a third was knocked down near Wycombe on January 21, 1868 (Zool.
1868, p. 1178). About the middle of October 1877 a small Petrel (said to have
been this species) was seen flying against a mill at High Wycombe, but recovered
and flew away (Field, 1877, October 20, p. 441). In November 1880 a Storm-
Petrel was picked up near Wendover (H. H. Crewe, Zoologist, 1881, p. 68).
153 (320). LEACH'S FORK-TAILED PETREL. Oceanodroma leucorrhoa
leucorrhoa. (Vieill.).
B. of Berks, and Bucks, p. 217.' Vict. Hist, of Bucks, p. 152.
Rare straggler ; three occurrences prior to 1868, two subsequently.
" After a strong gale of wind in the summer of 1847 or 1848, a man named
William Hibbs noticed a bird fluttering against a lamp at the corner of Brocas
Lane, Eton ; he caught it, and it proved to be a Petrel of this species." " It
appeared extremely thin, and was very weak, although in good plumage." " The
Rev. Bryant Burgess, of Latimer Rectory, near Chesham, sent me an account of
one of these rare Petrels which was taken in that neighbourhood. Upon the 1st
of November, 1859, during a very strong gale of wind, Mr. Poulter, gardener
to Lord Chesham, found a Fork- Tailed Petrel lying upon the ground in the deer-
park at Latimer. * * * The stomach was empty, the whole frame was very
thin and emaciated, and it was much battered about the head. * * * Another
specimen was picked up in an exhausted state at Woughton, Buckinghamshire."
One was caught alive in a hedge at Bierton, after the great gale of October 14,
1881 (A. H. Cocks in lift.). This specimen is mounted in the Rectory, Maid's
Moreton, near Buckingham (W. K. Clay in lift.). Mr. E. Hollis obtained for
the Bucks County Museum a specimen from Mr. Littlechild Sleeper, in Westcott,
which had been caught early in November 1910, having been mobbed by Rooks.
[GREAT SHEARWATER. Puffiuns gravis O'Reilly.
Mr. Archibald Allen, writing in the Field (October 28, 1911, p. 968), records
a Greater Shearwater, Pujfinus major, as having been killed by striking telegraph
wires " a few weeks since " near Olney. No investigation appears to have been
made as to whether the specimen in question was correctly identified, and the
date suggests the probability of confusion with the Manx Shearwater, which
frequently occurs inland during September, though, curiously enough, there
appears to be no record of this species from Bucks.]
224 Novitates Zoolooicae XXVII. 1920.
154 (336). GREAT CRESTED GREBE. Podiceps cristatus cristatus (L.).
B. of Berks, and Bucks, p. 65. Vict. Hist, of Bucks, p. 152.
Locally numerous breeding species on reservoirs, but few remain throughout
winter.
As is well known, the breeding- range of this Grebe has been extending during
the last twenty years or more. The Rev. H. H. Crewe informed Clark Kennedy
that he noticed a bird on Marsworth Reservoir in May 18(34. In the sixties it
began to breed on the Tring Reservoirs, but it was then a rare bird. The first
nest was found and the eggs taken by Miss E. Williams in 186T (Miss Ellen
Williams in litt.). It is now a very common breeder on the Marsworth and
Wilstone and also on the Halton (Weston Turville) Reservoirs. From state-
ments by the keeper, the Hon. Walter (now Lord) Rothschild recorded (Trans.
Herts. Nat. Hist. Soc. vol. v. p. 81) on the Tring Reservoirs for 1884 not less
than seventy- five nests, forty- five for 1885, forty- three for 1886, and that 115
birds were seen in April 1887. These numbers were, of course, approximate,
but may not have been exaggerated. In 1918 Street thought that about thirty
pairs or more nested. The number varies, and the breeding pairs diminished
greatly during the dry summers at the beginning of this century, when the reeds
were dry ; but now, since the water has been very high for several years, their
number has much increased again, and the bird will always hold its own,
as it is strictly protected. Mr. Oldham sent the following very interesting,
full notes :
" Most of the birds have left by end of October, but unless there is hard and
continual frost a few stay at Tring and Weston Turville through the winter.
(Eight on December 18, 1910, stayed until January 12, 1911, when heavy frost
drove all but one away ; about ten all through December 1912 and January
1913; nine on December 20, 1914 ; eight on December 26, 1915 ; twenty at least
on December 8, 1917, but frost in January 1918 drove all but two away.) The
birds begin to return about beginning of third week in February (twelve on
February 19, 191 1 ; thirty on February 22, 1914 ; nineteen on February 21, 1915 ;
thirty-three on February 20, 1916), but in the backward spring of 1917 they were
later : none to be seen on February 25. and only about a dozen on March 4.
" In February and March there are usually a good many birds that show no
signs of breeding-plumage (the majority are in full breeding-dress by middle of
February). I take it that this species does not breed in its second year, and that
these clean- necked birds are young of the previous year. I have often noticed
animosity shown to them by the adults, and believe they are all driven off the
waters by the adults before the actual nesting- season.
"In Brit. Birds, vol. iii. pp. 30-1, I recorded nestlings at Weston Turville
on May 2, 1909, but since then have seen still earlier young, e.g. at Wilstone on
April21, 1912, and at Marsworth on April 27, 1913."
Mr. L. W. Crouch (Br. Birds, vol. i. p. 327) records a nest found on May 20,
1907, on a reservoir near Aylesbury, containing the unusually large number of
seven eggs.
On the Thames it is only seen occasionally during the winter, and does not
breed either here or on the Stanwell Reservoir, where, however, it is a common
winter visitor (E. E. Pettitt).
N'OVITATES ZOOLOQIOAE XXVII. 1920. 225
155 (338). RED-NECKED GREBE. Podiceps griseigena griseigena (Bodd.).
B. of Berks, and Bucks, p. 209. Vict. Hist, of Bucks, p. 152.
Rare winter visitor.
According to Kennedy (I.e.), a specimen was shot at Saunderton, near Ris-
borough, October 10, 1848. The late C. E. Stubbs, of Henley, stated that it was
occasionally met with on the Thames : one shot at Greenlands " some years ago "
(i.e. prior to 1872) ; cf. Zoologist, 1903, p. 453. (The Rev. H. H. Crewe stated this
species " had once been obtained at Tring," but, as so often, gave no particulars.)
Oldham observed an immature bird, with the neck still retaining some stripes,
on Wilstone Reservoir, December 18, 1910. There was a Slavonian Grebe on
the water on the same day. Oldham further observed an adult, assuming summer
dress, on Wilstone Reservoir, March 16, 1913. He saw this bird on several occa-
sions up to and including June 22, 1913 (Brit. B. vol. vi. p. 374). Another adult,
assuming summer dress, was seen by the same observer on Tringford (Little
Tring) Reservoirs, February 8, 1914. This bird was picked up dead February
10, showing signs of an old wound on one wing, and with a broken tarsus. Mr.
Oldham thinks this was probably the same bird which he observed so often in
the spring of 1913, but if so it is curious how it had escaped his and other people's
notice in the interval between June 22, 1913, and February 8, 1914.
156 (337). SLAVONIAN GREBE. Podiceps auritus (L.).
B. of Berks, and Bucks, p. 132. Vict. Hist, of Bucks, p. 152.
Bare winter visitor.
Clark Kennedy records two specimens obtained near Windsor in 1858,
another killed on January 17, 1861, below Windsor Weir, and a fourth shot in
the winter of 1865 near Cookham Bridge. He also mentions a specimen killed
December 9, 1867, on the Thames at Eton, and he " heard of another specimen
which was shot on the Thames close to Eton " about the same time.
Mr. Heneage Cocks's gardener shot one at Great Marlow " in the sixties."
According to Rothschild two specimens were shot at Halton Reservoir between
1874 and 1880. They were first identified by the late Rev. H. Harpur Crewe,
and were afterwards seen by the present Lord Rothschild in a keeper's possession
near Halton. Unfortunately we have not been able to find out what became of
them.
On March 14, 1909, Mr. Oldham observed an adult in winter plumage, but
showing incipient ear-tufts and a tinge of chestnut on the flanks, on Wilstone
Reservoirs. The bird was still there on March 21 (Brit. B. vol. ii. p. 426).
Another specimen was observed by Oldham, December 18, 1910, and an adult
also on Wilstone Reservoirs on April 1, 1917, and several times on the 8th and 9th.
It was beginning to assume summer dress ; the flanks were tinged with chestnut,
the cheeks ashy.
On the Stan well Reservoir Mr. E. E. Pettitt saw a single bird from December
25, 1913, to January 25, 1914, and also noticed another early in 1915 at the same
place.
15
226 Novitates Zoolooicae XXVII. 1920.
157 (339). BLACK-NECKED GREBE. Podiceps nigricollis nigricollis Brehm.
B. of Berks, and Bucks, p. 210. Vicl. Hist, of Bucks, p. 152.
Black-necked Grebes were obtained on the Tring Reservoirs as long ago as
1 846 or 1 847 ; the specimens were mounted and seen by the present Lord Roth-
schild, but their whereabouts are now unknown. The statement by Kennedy
(p. 210, under the name of P. auritus) that it nested on the reservoirs, however,
was an error, due to the name " Eared Grebe " being used for this and other species
as well : the eggs taken by Mr. Williams were those of the Great Crested Grebe.
The Black-necked Grebe, however, has appeared from time to time on the re-
servoirs in the autumn and spring, but as an irregular and uncommon visitor only.
There are specimens in the Tring Museum from November 24, 1903, November
19, 1908, November 21, 1908, and April 23, 1909. Mr. Oldham observed speci-
mens on April 18, 1909, November 5, 1911, December 26, 1915 (probably of this
species), and January 20 and 27, 1918.
Mr. Oldham was the first to observe these birds breeding on the reservoirs
in 1918, and he published, among others, the following most interesting notes
in the Bull. B. 0. Club, vol. xxxix. pp. 28-34 :
" On April 28, 1918, I noticed two birds in full breeding-plumage, obviously
from the slight difference in size a pair, swimming in close company on one of the
reservoirs, and it was with a very lively interest that my sister-in-law, D., and
I saw them again at the same place on May 4 and 14, for their sojourn suggested
that possibly they would settle down and nest. Three days later D. saw four
birds, and on the 21st a party of seven — three pairs and an unattached male.
I had these seven birds under observation for some hours on the 26th. For the
most part they fed in close proximity — indeed, at times a blanket would have
covered the whole party, — but now and then a pair would detach themselves
from the others and go off on a short cruise. Essentially sociable as the birds
were, the odd male was treated with some intolerance, for at times one of the
others made a rush at it as though to drive it off. That the birds, although
paired, should at the end of May maintain this close association and
spend hours together fishing in the open water was puzzling, for although
from the first there had been indications of nuptial display — of which moro
hereafter — there was nothing to suggest that nesting had actually begun, and
at the breeding- place described in 1904 by Mr. O. V. Aplin (Zoologist, 1904,
pp. 417-420), which is now generally known to be in Wales, young are often
hatched at the beginning of June. The association that had obtained during
the second half of May did, however, break down at the end of the month, for
on June 1 the three pairs were feeding in different parts of the reservoir, whilst
the unattached male was cruising alone, and after that date we only saw the
birds singly or in pairs. By June 6 a pair had moved to one of the other reser-
voirs, and later in the month another pair frequented the place for a day or two.
On the 26th D. saw two birds, not mates apparently, fishing at some distance
apart on this water. One of them went repeatedly into a thick bed of Typha,
always at the same spot, behaviour which the head keeper noticed too on the 29th.
The inference was that the bird was feeding a sitting mate, or more probably
newly-hatched young, on the nest. The reservoirs are fringed in places with
broad dense beds of reeds and Typha angustijolia — admirable nesting- places
N0V1TATE9 ZOOLOGICAE XXVII. 1920. 227
for Grebes, — and, although the keepers by Lord Rothschild's orders were on the
look-out for nests, it is hardly a matter for surprise that none was seen, for the
recesses of the reed-beds could only have been explored at the risk of disturbing
the birds.
" On the last day of June a pair and an unattached bird were swimming in
open water on the reservoir which the whole party had frequented during May.
Even at a considerable distance one of this pair looked much more bulky arid sat
higher in the water than its mate, and I suspected that it was carrying young.
This suspicion was strengthened when its mate swam towards it with food in
its mouth and passed the food to something on its back. With the telescope we
could plainly see the heads of young ones protruding above the raised wings of
the bulkier bird, but it was impossible to tell at the distance how many young
there were. Once during the two hours we were at the place a single young one
swam clear of the parent for a minute or two and then clambered up again over
its tail. Except for a few brief intervals the other parent was constantly bringing
food to the young, diving in the shallow water close to its mate. It stayed under
water for only a few seconds at a time, and so achieved several journeys per
minute ; indeed, its industry and activity were astonishing compared with the
more leisurely tactics of the Great Crested Grebe when feeding young. Although
I never ascertained how many young were hatched out by this pair — it is certain
that there was more than one chick on the back of the old bird on June 30 — it
may be that only one was reared, for in the latter part of July I could never detect
more than one, with an old bird always in close attendance. On August 11, by
which time it was well grown, this young bird was fishing on its own account,
and I could see nothing of either parent.
" Four days after our first sight of this brood D. saw a pair with newly
hatched young on the other water, at the edge of the Typha-bed and close to the
spot where she had seen the bird go in on June 26. We spent some time watching
this pair at close quarters on the afternoon of July 6. The three chicks were
carried on the back of one parent and fed in that position by the other, which
came at frequent intervals with a small fish held crosswise in its bill. Now and
then on the approach of the old bird with food a chick would slide into the water
from the back of the nursing bird, only to regain its cradle quickly by climbing
up over its tail. Once the bird that was carrying the young shook them off its
back and dived. They swam immediately to the other bird, clambered up over
its tail, and the roles of the old birds were reversed. A fortnight later the division
of labour still obtained, but its mode had changed, for then one parent had sole
charge of two and the other of one of the clamorous and apparently insatiable
chicks, each party feeding independently of and at some distance from the other.
On August 4 the young birds were diving and fishing to some extent on their own
account, but most of the food was still caught by the old birds. By August 1 1
the young, which were then about two-thirds the size of the old birds, were scat-
tered about the reservoir and seemed to be quite independent of parental control.
A week later I could find neither old nor young, and can only conclude that
all the birds left the neighbourhood so soon as the young could fly— a proceeding
in striking contrast with that of the Great Crested Grebes, which do not leave
the reservoirs for the winter until the latter part of October. That two pairs
nested and reared broods is beyond question. It may be that the third pair
nested, but escaped notice — an easy matter if the total acreage of the reservoirs
228 NOVITATES ZOOLOGICAE XXVII. 1920.
is taken into account ; but after the party broke up at the beginning of June
little was seen of this pair or of the unattached bird.
" As few people in this country have any first-hand acquaintance with the
Black-necked Grebe in its nesting-haunts, some extracts from my note-books
regarding the appearance and behaviour of the birds may not be out of place.
" In life the silky yellow ear-coverts are not folded closely as represented
in most figures, but, radiating from a centre, occupy a third of a circle and show
as golden rays against the black cheeks. In conjunction with the upstanding
frontal crest, the tip-tilted bill, and crimson eye, they contribute not a little to
the bizarre appearance of the bird. The young for the first few days are much
darker in colour than Great Crested Grebes of the same age and resemble young
Dabchicks, but the stripes on the neck and body are more obscure than in either.
At four weeks the stripes on the body are imperceptible and those on the neck
difficult to make out, even with a glass, at a distance of a few yards. The birds
are then dark ash-grey with fore-neck, breast, and cheeks white, and at a little
distance look like young Coots rather than Grebes. Their rate of growth is
astonishing. A couple of days makes a perceptible difference in their size and
at six weeks they are more than two-thirds the size of the adults. The rate of
growth in the Great Crested Grebe, and I think the Dabchick too, is much slower.
The curious habit that Grebes have of protruding and wagging a foot behind them
is practised early in life, for several times we saw a young one do so whilst on the
old one's back.
" Before nesting actually began there was evidence that the Black-neck
engages in nuptial displays akin to those of the Great Crested Grebe, but unfor-
tunately the performance which Mr. L. Huxley (P.Z.8. 1914, pp. 491-562) calls
a ' shaking bout,' although often observed, was always engaged in at too great
distance for details of pose and of the disposition of the plumage to be appreciated.
Mr. Aplin (loc. cit.) refers to a bout between two birds that had a young brood,
and such a thing may be not uncommon ; it certainly is not in the case of the Great
Crested Grebe. On May 19 a bird — I think, a male — brought to the surface
what looked like a piece of matted alga, and swimming up to its mate proffered
the morsel, an action probably connected with courtship, whilst on May 21,
D. saw two of the birds ' stand up in the water on their tails, facing one another
and shaking and bowing their heads,' a performance obviously analogous to
the ' penguin-dance ' of the Great Crested Grebe described by Mr. Huxley.
" The paired birds usually kept close together, but sometimes when fishing
they became separated and would then call to one another with a plaintive pee-eep,
a note which Naumann (Nat. Vog. Deutschl. vol. ix. pp. 768-84, 1838) renders
beeb. That author describes as bidder, vidder, vidder, vidder, another note which
is very like the rippling cry of the Dabchick, though lacking perhaps something
of its trill. In Wales I have heard a harsh creaking note strongly reminiscent
of the call of the Partridge, and probably the analogue of the groaning croak which
the Great Crested Grebe utters in the spring. The alarm-note resembles the
whit of the Dabchick, but it is neither so loud nor so sharp. The hunger-cry of
the young, uttered incessantly as they follow the old birds for food, is similar in
general character to that of the Great Crested Grebe, which Mr. W. P. Pycraft
(The British Bird Book, vol. iv. p. 427) aptly renders as pee-a, pee-a, pee-a, and
of the Dabchick, but is not quite like either. The difference, although difficult
to express in words, was apparent enough when the young of all three species
Novitates Zoological XXVII. 1920 229
were calling at once in close proximity. The hunger-cry of the Dabchick is shriller
and more quickly iterated than that of the Great Crested Grebe and lacks
something of its querulous tone.
" When feeding, the birds are more under water than on the surface. Half a
dozen dives in deep water, not consecutive but taken at random, timed 25, 26,
23, 27, 28, and 26 seconds respectively, but in shallow water and particularly
when the old birds are feeding young the duration is often much less. So far
as I could judge the young were fed exclusively on small fish, but when old enough
to forage for themselves they took other food as well. They picked something,
apparently small insects, from the surface of the water, and on one occasion one
brought from the bottom what looked like a large drowned earthworm and
swallowed it.
" The birds evinced little fear of people walking on the reservoir banks and
merely swam out for a few yards if anyone passed when they were feeding close
inshore. When encumbered with a brood this indifference was even greater,
and they would feed the young ones with apparent unconcern, although people
were standing and watching them at a distance of a few feet. I was standing
one afternoon at the water's edge looking at an old bird with two young ones.
On two occasions this bird came to the surface just at my feet. It did then
evince some alarm ; uttering a cry, whit, whit, whit, it rushed through the water
for a yard or two with body submerged and head and neck only protruding, then
dived again just as the Great Crested Grebe does under similar circumstances.
This discomposure was, however, only momentary, and the bird resumed the
even tenor of its fishing without more ado."
In 1919 three, if not four, pairs returned to the reservoirs. According to
Mr. Oliver G. Pike's observations (Brit. B, vol. xiii. p. 146, 1919), one pair was
driven off from Marsworth Reservoir, where only one remained to breed. They
had eggs by the middle of May, but the eggs disappeared, either being taken by
a rat or Moorhen, or possibly by an unscrupulous egg-collector, who might easily
have been guided to the nest by the conspicuous " hide " erected near the nest
by Mr. Pike and a keeper, for the purpose of photographing nests and birds,
which, as the photographs published in Country Life, Brit. Birds vol. xiii., and
the accompanying plate show, was most admirably accomplished by Mr. Pike,
at the second nest, which contained eggs early in June, the first egg being hatched
on June 20. The birds on the other reservoir must also have hatched, but no
exact dates are available. We have no doubt that these birds will now again
return and regularly nest on the reservoirs, which are well watched by interested
keepers, so that egg-collectors, if they should attempt to find eggs, will have
small chance. In 1920 a specimen was seen on March 28 !
158 (340). LITTLE GREBE or DABCHICK. Podiceps ruficollis ruficollis (Pall.).
B. of Berks, and Bucks, p. 67. Vicl. Hist, of Bucks, p. 152.
Common resident on ponds and reservoirs.
Breeds in considerable numbers on the reservoirs, especially on those at
Tring and Halton. It also nests commonly on the Thames from Boveney to
Hambleden, and a pair or two may be met with on almost any suitable piece of
water. Some leave the reservoirs and other inland waters for the rivers, which
remain open, but many remain throughout the winter.
230 NOVITATE3 ZoOLOaiCAE XXVII. 1920.
159 (341). GREAT NORTHERN DIVER. Colymbus immer Briinn.
II. of Berks, and Ducks, p. 210. Vict Hist, of Bucks, p. 151.
Bare winter visitor to the Thames and reservoirs.
In the Dinton Hall MS. is a description and figure of an adult bird found
by William Saunders in the neighbourhood on December 3, 1774. Dr. Lamb
records one under the name of C. glacialis from Maidenhead in January 1794,
and also a second, evidently an immature bird, as C. immer, shot at the same place
and at the same time (cf. Zoologist, 1880, p. 317). In December 1841 another
immature specimen was obtained on the Tring Reservoirs ; while what is described
as a " young one " was captured alive in a ditch at Chequers Court on May 9,
1850. In November or December 1859 a specimen was procured at Chesham,
according to the Rev. B. Burgess. W. B. Botting records a specimen bought
by him, which had been recently killed on the Thames near Great Marlow {Field,
December 9, 1865, p. 426) ; and H. Noble states that one was killed near Temple
Island, below Henley, in 1865, and is now in the possession of Mr. W. D. Mackenzie,
of Fawley Court (Vict. Hist, of Berks, vol. i. p. 165). Another was also killed
near Henley (but apparently just outside the county boundary) on November
18, 1872 (C. A. Sheppard, Field, November 30, 1872, p. 530).
On the reservoirs the keeper, James Street, observed one on February 15,
1886. Rothschild also informed Littleboy that one was shot in November
1885, and another on January 1, 1887 ; while another is said to have been seen
in the following month (cf. Trans. Herts. Nat. Hist. Soc. vol. iv. p. 166, vol. v.
p. 83, vol. ix. p. 159 ; and Vict. Hist. Herts, vol. i. p. 216).
E. E. Pettitt informs us that there is a specimen at the " Angler's Rest,"
at Egham, which was shot by E. Hanks at Bell Weir in 1889. Street also reported
another as seen on the reservoirs on January 12, 1897 (Trans. Herts. Nat. Hist.
Soc. vol. x. p. 40).
In the winter of 1905-6 E. E. Pettitt also noted one on the Stanwel
Reservoir, just over the Middlesex boundary.
On November 2, 1913, Oldham observed a restless bird on Wilstone Reservoir.
"It frequently took flight, going from one part of the reservoirs to another.
Finally it rose in circles until it became a mere speck in the sky, and then dropped,
as I thought to Marsworth Reservoir, but I could not find it, when later I searched
that water" (Oldham in litt.). It was almost certainly this bird which was
picked up dead near the reservoirs November 8, 1913. The bill was damaged
at the base, probably by shot, or possibly by striking a wire.
160 (343). BLACK-THROATED DIVER. Colymbus arcticus arcfacus L.
A female was shot by the present Lord Rothschild on Wilstone Reservoir,
December 27, 1910, and is in the Tring Museum.
161 (344). RED-THROATED DIVER. Colymbus stellatus Pontoppidan.
B. of Berks, and Bucks, p. 134. Vict. Hist, of Bucks, p. 151.
Bare winter visitor.
According to Kennedy, I.e., this species was formerly the commonest of
the three Divers, and specimens used to be killed almost annually on the Thames
NOVITATES ZOOLOGICAE XXVII. 1020. 231
near Windsor, Eton, and Datchet, occasionally at Maidenhead and Cookham, and
once near Burnham. He states that most of the birds obtained are immature.
There seem, however, to be no definite records from the river since 1864. They
are very rarely seen on the Tring Reservoirs.
On January 10, 1909, Oldham watched a specimen for some time on Wilstone
Reservoirs (Zoologist, 1909, p. 77), where he also saw an adult on July 3, 1910.
A female was shot on the Reservoirs, January 14, 1910, which is in the Tring
Museum.
The late Dr. Eagles, of Aylesbury, presented a mounted specimen to the
Bucks County Museum in 1910, which he said he had shot himself " some years
before " near Aylesbury railway-station.
162 (345). WOOD-PIGEON. Columba palumbus palumbus L.
B. of Berks, and Bucks, p. 54. Vict. Hist, of Bucks, p. 146.
Common resident ; great increase in winter.
Breeds everywhere in woods and parks. In winter appears in great flocks,
wherever beech-mast is plentiful, but during the last twenty-seven years has never
been so numerous as in the winter of 1894-5.
[ROCK-DOVE. Columba livia livia L.
Vict. Hist, of Bucks, p. 146.
In 1902 Mr. A. Heneage Cocks wrote to Hartert as follows : "A wild, white-
rumped Pigeon, slightly smaller than the Wood-Pigeon, and equally distinct
from the Stock-Dove, is, or was, plentiful at one particular spot in Buckingham-
shire, viz. a high chalk cliff, facing the Thames near the lower end of the Danes-
field estate, near where Harleyford estate adjoins. These birds could always
be seen flying thence over the river, and I have shot specimens, but never since
I began collecting, and for some years now shooting has been stopped on the
river, and I cannot say whether they are still there, but see no reason to the
contrary." Mr. Cocks also had a good view of a white-rumped bird at Little
Marlow, which rose from a gravel-pit by the roadside.
As feral Pigeons are often almost indistinguishable from wild Rock-Doves,
it is difficult to say whether these Pigeons were really originally wild birds or
feral, though in the latter case all the individuals in a colony are not as a
rule alike.]
163 (346). STOCK-DOVE. Columba oenas oenas L.
B. of Berks, and Bucks, p. 55. Vict. Hist, of Bucks, p. 146.
Resident, common though local.
Not rare generally where old trees afford nesting-places. Hartert (I.e.)
supposed that Stock-Doves were migrants, because they are migratory in the
northern parts of the continent, leaving their nesting-places in the autumn and
returning to them early in March, if not before. They are, however, resident
in the British Isles. Hartert also doubted the statements of Kennedy and H. H.
Crewe, who reported " large flocks " and "great numbers" feeding upon beech-
mast, and probably not without reason, though they flock together to some extent
232 NOVITATES ZOOLOCICAE XXVII. 1920.
in winter, as Oldham observed about twenty feeding on a fallow near Hastoe
on April 25, and a flock of eleven on March 31, 1917, in a field near Wilstone
Reservoirs. As at that time Stock-Doves in many cases have already eggs
and certainly are paired at their breeding-places, these flocks (though not " large ")
were possibly migrants from the north of the continent.
164 (348). TURTLE-DOVE. Streptopelia turtur turtur (L.).
B. of Berks, and Bucks, p. 94. Vict. Hist, of Bucks, p. 147.
Summer resident.
Seems to be not rare in all well- wooded parts and to have increased lately
in several places. Breeds in considerable numbers in the Thames Valley. Mr.
A. H. Cocks noted a great increase in the numbers of this species about twenty-
five years ago. Like the Wood-Pigeon, the Turtle-Dove is at times attacked by
diphtheria, and one was picked up by Mr. A. H. Cocks at Skirmett on July 31,
1908, which had evidently succumbed to this disease.
[INDIAN SPOTTED DOVE. Streptopelia chinensis suratensis (Gm).
B. of Berks, and Bucks, p. 95.
Donovan, Nat. Hist. Brit. B. vol. vii. pi. 149 and text (1816), figures and
names " Columba albinotata " * specimens of 8. chinensis suratensis that passed
into his collection from the Leverian Museum, said to have been shot in Bucking-
hamshire, where, according to Latham, they had not been rare. No doubt these
birds, which like other Doves are often kept in cages in the East, were " intro-
duced by some fortuitous circumstance into the vicinity of Buckinghamshire,'5
as Donovan wrote.]
165 (350). PALLAS' SAND-GROUSE. Syrrhaptes paradoxus (Fall).
Vict. Hist, of Bucks, p. 117.
Exceptional visitor ; no specimen shot in Bucks seems to exist.
Mr. A. F. Grossman writes (in litt.) : " During the visitation of this species
in 1888 my grandfather saw a flock of birds at Farnham Royal, which from his
description were undoubtedly of these birds. I was unfortunately unable to
see them on going to the place about an hour afterwards." F. Bond recorded
a flock of about a dozen birds as seen on June 19, 1888, near Staines Moor, on
the borders of Bucks, and Middlesex (Zoologist, 1889, p. 227). Rothschild believes
that he saw three flying overhead when shooting near Halton in 1896, but as it is
not known that any visited Europe that year, we fear that a mistake was made.
Edwin Hollis saw three birds, 28 . viii . 1908, flying over the road between
Wendover and Aylesbury, which he took to be Sand-Grouse. They were certainly
not Partridges, he says.
On December 1, 1908, Rothschild recorded a flock of seven or eight of these
birds which rose out of a turnip-field in the parish of Buckland, on the Bucks,
and Herts, boundary, near Tring, while Pheasant-shooting (Brit. Birds, vol. ii.
p. 309).
• This name has been overlooked in the Cat. B. Brit. Mus. vol. xxi., and other synonymic lists.
Novitates Zoolooicae XXVII. 1920. 233
166 (352). STONE- CURLEW or THICK-KNEE. Burhinus oedicnemus
oedicnemus (L.).
B. of Berks, and Bucks, p. 97. Vict. Hist, of Bucks, p. 148.
Summer visitor in greatly reduced numbers, breeding very locally.
Formerly this interesting species bred in some numbers on the slopes of the
Chiltem Hills, and also on the chalky uplands near Ivinghoe. The late C. E.
Stubbs had eggs taken at Fawley on May 23, 1860 (cf. Zoologist, .1903, p. 450).
In Clark Kennedy's time its numbers had apparently already been diminished,
but H. Harpur Crewe reported that it might still often be heard wheeling over-
head on a summer's night at Drayton Beauchamp. Bryant Burgess also stated
that its note had been heard near Chesham ; and Kennedy mentions occurrences
near Aylesbury, Buckingham, and several times at Slapton.
About 1900 Mr. A. H. Cocks found it still numerous in summer on the east
side of the Chilterns near Skirmett, and from there to Turville Heath and across
the Oxfordshire border. He relates how the birds used to spend some hours
after sunset flying backwards and forwards past his house screaming, from the
end of May onward. About the year 1909 or 1910 a great diminution in their
numbers seems to have taken place (Brit. Birds, vol. viii. p. 173). Heatley Noble
(loc. cit.) also states that up to 1905 one or two pairs bred regularly on a part of
the Fawley Park estate. There are, however, entries in Mr. A. H. Cocks's diary
of occasional appearances of this species up to much later dates. Three or more
were heard on April 13, 1908, and again on the 17th, and others are noted under
the dates of May 13, 1912, and August 8, 1913. The Bucks County Museum
also contains an immature bird with the following inscription : " Bred on borders
of Hambleden and Turville parishes. Captured with broken wing, 20.vii.1907 "
(E. Hollis in lift.).
A clutch of eggs now in the Aylesbury Museum was taken in May 1910 in
the Saunderton district, and in April 1914 another nest with eggs was found and
photographed, which hatched off successfully (E. Hollis, Brit. Birds, vol. viii.
p. 121). According to the farmer the birds still breed in this locality annually
(E. Hollis in lilt.).
Although the Stone-Curlew is not now known to breed on the Ivinghoe
Downs, it is worth noting that Hartert heard the unmistakable cry of this species
over Tring both in 1914 and 1915.
167 (351). OYSTER-CATCHER. Haematopus ostralegus ostralegus L.
B. of Berks, and Bucks, p. 184. Vict. Hist, of Bucks, p. 148.
Exceptional straggler.
Kennedy says that specimens have occasionally been killed on the Thames,
and instances one seen near Surley in March 1866, and another shot near Windsor
" a few years since." Mr. A. H. Cocks believes that he recognized the note
about midnight on August 8, 1S93, at Great Marlow. James Street shot a female
of the year on Little Tring Reservoir on September 7, 1897 (not September 24,
as stated in Trans. Herts. Nat. Hist. Soc. vol. x. p. 38). This specimen is now
in the Tring Museum. Street also told Oldham that he had seen one on March
20, 1915, at Marsworth Reservoirs.
234 NOVTTATES ZOOLOOICAE XAVU. 1920.
168 (356). DOTTEREL. Charadrius morinellus L.
B. of Berks, and Bucks, p. 140. Vict. Hist, of Bucks, p. 148.
Rare visitor ; no recent records.
This bird, like the Golden Plover, seems to have been of much more frequent
occurrence in former days. Being exceedingly good to eat and less shy than
most other Waders, they were apparently caught and shot a great deal. Kennedy
(I.e.) says that a few were shot in a field near Burnham in the spring of 1857,
and that they were rarely seen in the vicinity of Eton and Windsor, also that
they have been procured in the neighbourhood of Aylesbury and Drayton Beau-
champ. The late Rev. H. Harpur Crewe had an adult male which, together with
a female, was shot at Tringhoe, near Ivinghoe, August 14, 1862, by one of Earl
Brownlow's keepers (Ibis, 1862, pp. 390-1).
169 (358). RINGED PLOVER. Charadrius hiaticula hiaticula L.
B. of Berks, and Bucks, p. 141. Vict. Hist, of Bucks, p. 148.
Regular bird of passage.
Seen in suitable localities, except during the breeding-season and in the depth
of winter. Oldham sent the following notes about the reservoirs :
" Bird of passage at the reservoirs. If there is much mud a good many are
seen, but in seasons when the water is high there is no inducement for them to
stay. I saw none in 1916 or 1917.
"The spring passage apparently extends from mid-March to third week in
May (my outside dates are March 14 [1909] and May 21 [1911]).
" The autumn passage extends from end of July to third week in September.
(I have only once seen a bird in October, i.e. on October 13, 1907.) The birds
occur more frequently and in greater numbers in autumn than in spring. I saw
a party of ten, immature birds, on September 11, 1910 ; one of fourteen, adult
and immature birds, on September 18, 1910 ; and one of eleven, adult and im-
mature birds, on August 9, 1914.
"The birds often consort with Dunlins. Used to occur not infrequently
on the banks of the Thames, and probably does so now, though there are no
recent dates."
[KENTISH PLOVER. Charadrius alexandrinus alexandrinus L.
Although just outside our boundary, it seems wortli recording that G. W.
Kerr saw a Kentish Plover at the Stanwell Reservoir, Middlesex, on April 21,
1915 (in litt. to Pettitt).]
170 (362). GOLDEN PLOVER. Charadrius apricarius L.
B. of Berks, and Bucks, p. 114. Vict. Hist, of Bucks, p. 148.
Late autumn and winter visitor.
The Golden Plover was, according to accounts by sportsmen and farmers,
much more frequent formerly than it is now. We have no information of its
annual occurrence of late years near the reservoirs, where it is now only seen from
time to time in small flocks or singly, in winter. Several were shot near Aston
Clinton and Marsworth in November and December 1917. Flocks are often
Novitates Zoolooicae XXVII. 1920. 235
observed near Aylesbury, Princes Risborough, and Chesham, also near Bucking-
ham. Oldham observed a single bird, flying high, calling, near Marsworth on
July 13, 1910 ; he heard one December 5, 1915, and again on March 19, 1916,
and saw a flock of fifteen in a pasture near the reservoirs February 16, 1917.
In the Thames Valley it appears to be more numerous, and E. E. Pettitt
describes it as common in winter in the meadows between Taplow and Boveney.
171 (365). GREY PLOVER. Squatarola squatarola squatarola (L.).
Vict. Hist, of Bucks, p. 148.
Rare visitor.
On November 25, 1819, a Grey Plover was obtained near Dinton Hall.
According to Rothschild (information given to Littleboy) one was shot near the
reservoirs in March 1885. A male was shot by Hartert on the Wilstone Re-
servoir December 12, 1897, and is in the Tring Museum.
172 (307). LAPWING. Vanellus vanellus (L.).
B. of Berks, and Bucks, p. 59. Vict. Hist, of Bucks, p. 148.
Common resident.
The same birds seem to remain here throughout the year, but they assemble
in great flocks after the breeding-season. In severe winters they suffer badly,
and many die for want of food, as in the winter of 1917.
173 (370). RUFF. Philomachus pugnax (L.).
B. of Berks, and Bucks, p. 193. Vict. Hist, of Bucks, p. 150.
Occasional visitor.
A Ruff was shot at Dinton Hall August 8, 1774. One was killed near Ches-
ham in the sixties (Kennedy, I.e.). Single birds or small parties visit the Tring
Reservoirs from time to time. Grossman ( Vict. Hist, of Herts, vol. i. p. 213) records
specimens shot in August 1884 (one) and two in August 1886. Specimens shot
there on September 5, 1894 (<J), September 19, 1898, September 15, 1904 ($ ad.),
September 11, 1907 (? juv.), are in the Tring Museum. We know nothing of the
bird shot August 17, 1895, which is mentioned by Grossman {Vict. Hist, of Herts.
vol. i. p. 214). Mr. Oldham made the following observations : October 13 and
20, 1907, a young $ ; May 9, 1909, a female ; August 23, 1914, a young <J, feeding
on Mollusca (apparently Limnaea pereger) on the mud.
174 (371). KNOT. Erolia canutus canutus (L).
Rare visitor.
A young male was shot on the Tring Reservoirs on September 15, 1904,
and is in the Tring Museum. Mr. Oldham observed an adult bird, changing into
winter plumage, but still retaining a good deal of chestnut colour on the breast,
feeding with a Redshank on the mud at Wilstone Reservoirs, on September 12,
1909. A specimen was shot near Halton, January 28, 1911, and is mounted in
the Bucks. County Museum in Aylesbury.
236
NOV1TATES ZOOLOGICAE XXVII. 1920.
175 (372). SANDERLING. Crocethia leucophaea (Pall.).
B. of Berks, and Bucks, p. 184. Vict. Hist, of Bucks, p. 149.
Bare visitor.
According to Kennedy, from information by George Lillywhite, a specimen
was shot on the banks of the Thames not far from Surley Hall in the depth of
the winter of 1 866. According to Rothschild it occurred on the Tring Reservoirs
in 1886. An adult male was shot on August 18, 1902, near Drayton Beauchamp
by Mr. J. Horwood. The skin is in the Tring Museum. On May 9, 1909, Mr.
Oldham observed two Sanderlings with some. Dunlins and Ringed Plovers on
the mud at Startops End Reservoir. It must always have been a very rare bird,
and can never have been " fairly common " on the reservoirs, as reported to
Littleboy (Trans. Herts. Nat. Hist. Soc. vol. v. p. 78).
176 (373). DUNLIN. Erolia alpina alpina (L.).
B. of Berks, and Bucks, p. 145. Vict. Hist, of Bucks, p. 149.
Not uncommon passage migrant and occasional winter visitor.
Formerly not unfrequently seen on the banks of the Thames, but more
regularly on reservoirs and ponds, if there is sufficient mud to feed on, therefore
commoner when the water is low. Often consorts with other Waders, such as
Ringed Plovers, and other species of Erolia. According to Oldham (in litt.),
noticed from mid-March to mid-May, and again from mid-July to mid-October.
In the spring mostly in small parties from two to four, or singly ; in autumn old
and young often in parties of ten, twelve, and fourteen. Oldham observed Dunlins
on November 21, 1909 (one), December 7, 1913 (four), and November 15, 1914.
Hartert observed three in November and December 1915. A female shot on
December 2, 1916, is in the Tring Museum.
177 (374). CURLEW- SANDPIPER. Erolia ferruginea (Brunn.).
Vict. Hist, of Bucks, p. 149.
Passage migrant.
Three young birds were shot on the Tring Reservoirs September 3, 1892,
and a young female August 28, 1893. Mr. Oldhain sent us the following notes :
" A Curlew-Sandpiper and a Little Stint — both birds of the year — were
feeding with a party of six Ringed Plovers and ten Dunlins on the mud at Wilstone
Reservoir on August 29, 1909. Another Curlew-Sandpiper, or possibly the same
bird as I had seen on August 29, was feeding by itself on the mud at Startops
End Reservoir a week later. On August 27, 1911, a bird of the year was feeding
with four Dunlins at the same place. On September 20, 1914, two were feeding
with two Dunlins on the mud at Wilstone Reservoir."
178 (375). LITTLE STINT. Erolia niinuta minuta (Leisl.).
Viel. Hist, of Bucks, p. 149.
Occasional migrant.
Obtained on the Tring Reservoirs in August 1883 (not 1S85), and July 29,
1893, the latter specimen being in the Tring Museum. Mr. Oldham writes (in
litt.) :
N0VITATE3 ZOOLOOIOAE XXVII. 1920. 237
"August 29, 1909. — A Little Stint and a Curlew-Sandpiper — both birds of
the year — feeding with a party of six Ringed Plovers and ten Dunlins on the mud
at Wilstone Reservoir.
"September 18, 1910. — A Little Stint with a Dunlin and fourteen Ringed
Plovers on the mud at Wilstone Reservoir.
"August 23, 1914. — A Little Stint with a Redshank and three immature
Ringed Plovers on the mud at Startops End Reservoir. At Wilstone another
Little Stint was feeding with two adult and one young Dunlin.
[TEMMINCK'S STINT. Erolia temminckii (Leisl.).
In Trans. Herts. Nat. Hist. Soc. vol. v. p. 78, J. E. Littleboy wrote : " A
Temminck's Stint was shot on the reservoirs in September 1887. It is preserved
in Mr. Rothschild's collection." At that time local birds used to be stuffed by
the late A. Minall. There are now two mounted specimens of Temminck's Stints
evidently stuffed by Minall, one bearing under the stand the note " Rye," the other
" Thames." Whether one of these was at the time supposed to be from the
reservoirs, or whether the specimen has been destroyed, like the Marsh- Sandpiper,
when attacked by moths, cannot now be ascertained.]
179 (387). COMMON SANDPIPER. Tringa hypoleuca L.
B. of Berks, and Bucks, p. 98. Vict. Hist, of Bucks, p. 150.
Common bird of passage, breeding in small numbers.
Apparently nests near suitable watercourses, such as the Chess, Colne, and
possibly the Thames. Mr. Oldham writes (in lift.) : " Regular bird of passage
at the reservoirs from mid-April to third week in May, and again from end of
July to mid-September. The earliest date in spring, during the past ten years,
is April 9, and that, curiously enough, was in the inclement spring of 1917. I have
only once observed specimens so late as October, i.e. on October 3 and 10, 1915."
Although it is probable that a few pairs breed in the Chess Valley, there is
no recent definite proof. Clark Kennedy states that it breeds near the Chess
and Colne, and in Yarrell (4th ed. vol. iii. p. 447) the Editor says : " It is believed
to have nested in Kent and in Buckinghamshire." As, however, isolated instances
of nesting have been reported from Hertfordshire and Oxfordshire, there is no
reason why a few pairs should not breed in Buckinghamshire.
180 (389). WOOD-SANDPIPER. Tringa glareola L.
B. of Berks, and Bucks, p. 191. Vict. Htst. of Bucks, p. 150.
Uncommon visitor.
Kennedy mentions a specimen shot on Dorney Common near Eton in the
sixties, and another killed near Surley in the spring of 1867. Between 1892 and
1900 Hartert has observed several on the Tring Reservoirs, but the dates were
not noted. Littleboy (Trans. Herts. Nat. Hist. Soc. vol. v. p. 78) recorded a
specimen shot on the reservoirs in August 1886, on the authority of the Hon.
Walter Rothschild. The specimen cannot now be traced in the Tring Museum,
but at that time specimens used to be stuffed and the labelling left to irrespon-
sible persons and frequently omitted.
238 NOVITATES ZOOLOQICAE XXVII. 1920.
181 (390). GREEN SANDPIPER. Tringa ochropus L.
B. of Berks, and Bucks, p. 143. Vici. Hist, of Bucks, p. 150.
Rare bird of passage.
Kennedy mentions a specimen shot in the spring of 1859, near Chenies, in
Buckinghamshire ; another shot on Dorney Common, near Eton, in the autumn
of 1863, when a second specimen was seen at the same time. A pair was observed
frequently near Fawley, in December 1864, where one was shot on December
24, and another February 11, 1865. Two were also seen, and one shot, near Eton
in the winter of 1865, and others killed at Cookham and Surley in 1865 and 1867.
According^to the late Rev. H. Harpur Crewe, the Green Sandpiper has been
observed " to frequent the reservoirs and canals near Drayton Beauchamp in
small parties every winter," and a bird of this species was shot " many years
ago " near Risborough.
Possibly in Harpur Crewe's time the species may have been less scarce near
Drayton Beauchamp, when some of the canals which are now dry contained
water, but it was probably rare even then. In the Tring Museum is ,t specimen
shot near Long Marston by Mr. J. Chapman. Mr. Oldham observed it on
Startops End Reservoir on August 14, 1909, and near Wilstone Reservoir Sep-
tember 13, 1914. Street reported four May 12, 1897.
All through August 1918 single Green Sandpipers were seen by Hartert
on the mud of Little Tring and sometimes at Wilstone Reservoir. On August
11 Oldham saw three together at Little Tring; and E. E. Pettitt noticed one on
Ham Island, River Thames, on August 3 of the same year.
182 (397). MARSH- SANDPIPER. Tringa stagnates (Bechst.).
Vict. Hist, of Bucks, p. 150.
Exceptional straggler.
In October 1887 a specimen shot near the Tring Reservoirs was identified
by Lord (then the Hon. Walter) Rothschild as the Marsh-Sandpiper. Unfor-
tunately the mounted specimen was inadvertently burnt with a few other rare
birds in 1890 (cf. Brit. B. vol. iii. p. 356, footnote ; Hand-list Brit. B. p. 184).
183 (394). COMMON REDSHANK. Tringa totanus totanus (L.).
B. of Berks, and Bucks, p. 191. Vict. Hist, of Bucks, p. 150.
Breeds in small numbers, and is not rare on passage.
Not uncommon on passage in spring and autumn, but also sometimes ob-
served in winter. Has probably nested in small numbers for many years past.
A specimen was shot at Dint on Hall on August 11, 1774. A little over twenty
years ago Mr. Charles J. Wilson observed one and sometimes two pairs fre-
quenting the River Ouse, just above Olney, during the months of May and June,
for two or three years. " During May 1909, when the water was low, and there
was much mud in consequence, three or four clamorous birds were always to he
seen at Wilstone Reservoirs. On June 7 of the same year a pair was feeding on
the mud at the edge of a big patch of rushes with a brood of downy young. I
think another pair nested, but have no proof" (C. Oldham in litl.). In 1917
and 1918 several pairs were observed nesting in a meadow near Aylesbury by
N0TIT4TE8 ZOOLOOICAE XXVII. 1920. 239
Mr. Edwin Hollis. Three nests were found April 26 and 27, 1917, one April 27,
1918, the hen bird sitting. An egg is in the Aylesbury County Museum. In
1918 first seen March 23rd, in 1920 March 24th, in 1919 the first to return to
this breeding-place was a pair observed by Edwin Hollis on March 15. On
the Tring Reservoirs Mr. C. Oldham and Hartert have observed it as a bird
of passage, usually singly in March and April, and again from end of June to
end of August. It is rather an uncommon winter visitor, but Oldham observed
it on November 26, 1916, and Oldham and Hartert saw one walking on the ice
on Startops End Reservoir on January 6, 1918.
Possibly a pair may nest occasionally in the Thames Valley, for Pettitt
records this species from Ham Island on June 6, 1916, and thought that a pair
was breeding here, but was not certain.
184 (395). SPOTTED or DUSKY REDSHANK. Tringa erythropus (Pall.).
One observation oj a flock in 1918.
At mid-day, on August 25, 1918, Mr. Charles Oldham observed a party of
five Dusky Redshanks dropping to the mud at Little Tring Reservoir. They at
once began to feed in a large bed of Polygonum amphibium in three or four inches
of water. After being put up they returned in a minute or two, feeding assidu-
ously ; but after a stay of about an hour in all they got up, rose high in the air
and went clear away (Brit. B. vol. xii. p. 117, 1918). This is the first and only
record of the occurrence of this species in Herts., nor has it been observed in Bucks.
185 (396). GREENSHANK. Tringa nebularia (Gunn.).
B. of Berks, and Bucks, p. 145. Vict. Hist, of Bucks, p. 150.
Passage migrant.
Kennedy reports one as shot near Chesham, and states that it has occasionally
been obtained on the Thames. It also occurs on the Tring Reservoirs. Hartert
has seen it several times in autumn during the last twenty-five years, but omitted
to note the dates. Street saw it often in autumn and May. Oldham (in litt.)
calls it " a rather uncommon bird of passage at the reservoirs." He notes the
following occurrences :
9 . v . 1909, one at Startops End Reservoir.
12 . and 19 . ix . 1909, four at Wilstone Reservoir.
13 . and 27 . viii . 1911, one at Startops End.
23 . viii . 1914, one at Little Tring Reservoir.
6 . ix . 1914, one at Startops End.
13 . ix . 1914, one at Wilstone, the last three observations referring perhaps
to the same bird.
The species probably occurs every year.
186 (398). GREY PHALAROPE. Phalaropus fulicarius (L).
B. of Berks, and Bucks, p. 197. Vict. Hist, of Bucks, p. 149.
Rare on autumn migration and ill winter.
One was shot on the Thames at Windsor in December 1851, and another,
much exhausted, was seen on the river at Maidenhead in the autumn of 1867.
240 Novitates Zoologic.ve XXVII. 1920.
In the autumn of 1866 there was an extraordinarily large immigration to
England, and a specimen was then observed on the canal near Halton. A young
bird, moulting into winter plumage, was shot on Tring Reservoirs 20 . x . 1891 ;
a male was picked up in the woods near Tring, close to the boundary of Bucks.,
in December 1899 ; a female shot on Marsworth Reservoir 2 . xi . 1904 by Hartert,
another female 18. xi. 1911. These four specimens are in the Tring Museum.
(Crossman's statement that four were shot in October 1891 is apparently an
error ; at least we can only trace the one mentioned above.) Mrs. and Miss
Oldham observed a Grey Phalarope at the reservoirs September 29, 1919,
swimming and flying over from Marsworth to Startops End Reservoir.
187 (399). RED-NECKED PHALAROPE. Phalaropus lobatus (L.)
Vict. Hist, of Bucks, p. 49.
One specimen Tring Reservoirs, October 1885. Erroneously recorded as
Grey Phalarope (Ph. fulicarius) in Trans. Herts. Nat. Hist. Soc. vol. v. p. 83, 1890.
[The supposed instance of breeding of Black-winged Stilt (Himantopus
himantopus) in 1834 near Beaconsfield, recorded by Clark Kennedy (B. of Berks,
and Bucks, p. 192), is of course quite unworthy of credit.]
188 (402). BAR-TAHiED GODWIT. Limosa lapponica lapponica (L.).
B. of Berks, and Bucks, p. 192. Vict. Hist, of Bucks, p. 150.
Uncommon passage migrant.
There are very few records of this species. During the first week of May
1846 a pair of these birds was observed to frequent a field on the farm of a Mr.
Biggs, near Slapton. The hen bird was shot, and examined by the Rev. Bryant
Burgess, of Latimer (B. of Berks, and Bucks, p. 193, from a letter of Burgess).
One was shot on the reservoirs in December 1880 (Rothschild, Trans. Herts.
Nat. Hist. Soc. vol. v. p. 77). According to a letter from Mr. H. M. Roberts of
Ivinghoe a specimen was shot in the winter of 1895 near the brewery, at Ivinghoe.
An adult male in nearly full summer plumage was shot on Wilstone Reservoir
on May 6, 1907, by James Street, and is now in the Tring Museum. On April
29, 1917, Mr. Charles Oldham observed one feeding on swampy ground at the
edge of Wilstone Reservoir, which did not show any of the foxy-red colour of the
summer plumage.
189 (403). BLACK-TAILED GODWIT. Limosa limosa limosa (L.).
Rare passage migrant.
A young female was shot at Wilstone Reservoir 24 . vii . 1 893, a young male
15 . ix . 1904. Both are in the Tring Museum.
Littleboy, apparently from information by the Hon. Walter Rothschild,
says that one was shot on the reservoirs in September 1886 (Trans. Herts. Nat.
Hist. Soc. vol. v. p. 78, 1890 ; see also Grossman, Vict. Hist, of Herts, vol. i. p. 214).
The specimen is not preserved.
Novitates Zoological XXVII. 1920. 241
190 (404). CURLEW. Numenius arquata arquata (L.).
B, of Berks, and Bucks, p. 142. Vict. Hist, of Bucks, p. 150.
Passage migrant.
Curlews have been observed chiefly on spring and autumn migration, and
a few shot in many places of the county. They are heard almost every spring
passing over the Tring Reservoirs in the evening, and on October 16, 1907, Street
saw sixteen at the reservoirs.
Oldham made the following notes :
"July 21, 1912. — At 2.30 p.m. three Curlews came down to Wilstone Re-
servoir. They did not alight; but circled round the reservoir two or three times,
calling as they flew, and then rose and went off again. I lost sight of the birds
behind some trees, and cannot say which direction they took.
"March 2, 1913. — Wind W.S.W. ; a Curlew calling high overhead near Mars-
worth Reservoir at mid-day. After circling round for a few minutes, it alighted
in a field near the reservoir.
"January 2, 1916. — A Curlew going north-east, with the wind, near Marsworth
Reservoir."
191 (405). WHMBKEL. Numenius phaeopus phaeopus (L.).
B. of Berks, and Bucks, p. 143. Vict. Hist, of Bucks, p. 150,
Rare and irregular visitor.
The Rev. H. Harpur Crewe wrote (Kennedy, I.e.) : "A few specimens of
the Whimbrel are seen almost every winter on the banks of the reservoirs here,
that is to say, the Marsworth Reservoir, . . . The Weston Turville sheet of water,
and the canals at Halton and Wilstone." Kennedy also notes that it is occasion-
ally met with on the Thames in spring and autumn. Two were shot in the north-
eastern corner of Buckinghamshire, not far from the River Ouse, in the second
week of May 1894 (Aplin, Zoologist. 1894, p. 267).
Probably the Whimbrel was always very rare, and the statement " almost
every winter " not literally correct, as we have no recent evidence of its occur-
rence, except that Mr. Headley saw two Whimbrel (Numenius phaeopus) at
Tring on May 5, 1916 (Trans. Herts. Nat. Hist. Soc. vol. xvii. p. 40, 1918).
[GREAT SNIPE. Gallinago media (Lath.).
Vict. Hist, of Bucks, p. 149.
No proof of occurrence in Bucks.
The statement of the occurrence near Tring, in the Vict. Hist, of Herts, vol. i.
p. 213, of an albino Great Snipe is an error, this variety being one of the Common
Snipe. Among the numerous Snipe which Lord Rothschild and Hartert have
examined from the Tring Reservoirs there has never been a single Great Snipe.
In the Field, vol. xli. p. 135, February 8, 1873, A. H. Cocks wrote : " When
shooting with Mr. T. O. Wethered by the river side at Marlow in September
1871 (I think the 3rd), I saw a Great Snipe (O. major), but did not get it."]
16
242 NOVTTATES ZOOLOOICAE XXVII. 1920.
192 (409). COMMON SNIPE. Gallinago gallinago gallinago (L.).
B. of Berks, and Bucks, p. 115. Vicl. Hist, of Bucks, p. 149.
Resident, passage migrant and winter visitor.
Common in suitable localities from October to March, and on the Tring
Reservoirs a considerable passage takes place during the last days of March and
till April 12. These Snipe never drum and do not attempt to nest there, though
in one place the ground appears to be suitable. Kennedy states that nests
have been found several times on East Burnham Common. Alan F. Crossman
and Hartert heard Snipe drumming on Farnham Common in 1900 and 1901,
so that they may have been breeding there. Apparently nested near Halton
recently.
In the Thames Valley, while the Corncrake has to a great extent disappeared
from the meadows near the river, the Snipe has undoubtedly increased con-
siderably in numbers, as is also the case in the neighbouring counties of Berks,
and Oxon. Mr. E. E. Pettitt states that two or three pairs nest near Wraysbury,
and that this species also breeds near Marlow, Medmenham, and Hambleden.
[WILSON'S SNIPE. Gallinago gallinago delicata (Ord.).
Vict. Hist, of Bucks, p. 149.
No reliable evidence of occurrence in the British Isles.
Harting (Zoologist, 1872, p. 3273, id. Handb. Brit. B. p. 143) stated that
a specimen of the American Snipe, G. g. delicata (icilsoni of older authors), shot
at Taplow. Bucks., on August 1, 1863, had been forwarded in the flesh for identifi-
cation to Mr. Gould, in whose possession he had examined it. The case must
remain doubtful, and can hardly be accepted as correct. The American Snipe
is so similar to G. g. gallinago that single specimens cannot always be identified
with absolute certainty. The chief differences are : normally sixteen tail-
feathers in delicata, normally fourteen in gallinago, bill generally shorter in
delicata, mostly longer in gallinago, sharper and more regular black cross-bars
to the axillaries and under wing-coverts and usually cross-bars to the sides of
the breast in delicata. Sixteen tail-feathers, however, occur also sometimes,
and not so very rarely, in gallinago, and the bill as well as the cross-barrings differ
in both forms. Moreover, Harting specially states that the " wilsoni " which
he examined had only fourteen rectrices — thus lacking one of the chief charac-
teristics of G. g. delicata \ ]
193 (410). JACK SNIPE. Limnocryptes gallinula (L.).
B. of Berks, and Bucks, p. 110. Vict. Hist, of Bucks, p. 149.
Winter visitor.
A regular winter visitor and not rare, though far less numerous than the
Common Snipe. It frequents the same localities as the latter, but occurs also
on meadows and even on little bits of marshy ground among bushes and trees.
A well-marked spring movement has been observed annually near the Tring
Reservoirs, as in the Common Snipe, at the end of March and at the beginning
of April.
In the south of the county it seems to be much less frequently observed,
and Mr. A. H. Cocks remarks of one flushed on October 25, 1909, at Skirmett,
that it is the first seen by him there !
NOVITATES ZOOLOQICAE XXVII. 1920. 243
194 (411). WOODCOCK. Scolopax rusticola rusticola L.
B. of Berks, and Bucks, p. 114. Vict. Hist, of Bucks, p. 149.
Regular visitor in autumn and winter, but not numerous.
Woodcock generally arrive towards the end of October, and may be found
until the end of February, but they seem to be nowhere very common in Bucking-
hamshire. In the last months of 1919 they were more frequent than usual near
Tring and Halton. We have no recent records of their breeding in the county,
but they have nested near Beaconsfield and near Burnham (1867). In the sixties
a few birds bred near Stoke, Burnham, and Brickhill. According to Lord Roth-
schild a pair nested in the woods above Drayton Lodge, at the boundary of Herts,
and Bucks., about 1888, but the eggs were deserted, because one of the parents
was shot by a neighbouring keeper ! (sic !).
Mr. W. Dalziel Mackenzie informed Clark Kennedy that a Woodcock
disturbed on December 13, 1859, perched on a large oak, where it remained
for some time.
195 (412). BLACK TERN. Hydrochelidon nigra nigra (L.).
B. of Berks, and Bucks, p. 149. Vict. Hist, of Bucks, p. 150.
Not uncommon on passage.
In the Dinton Hall MS. occurs the passage : " These birds were shot by
Sir John van Hatten and the Rev. W. Nance on May 10, 1774, at Elthorpe."
It is a not unfrequent but somewhat irregular visitor to the Thames and other
large waters. Clark Kennedy records one from Risborough, and about a dozen
from the Thames Valley. It visits the Tring Reservoirs probably every year,
generally throughout May, but in the Tring Museum are specimens shot on April
22 and 27, while Oldham once saw three as early as April 19, 1914. The return
passage begins early in August and lasts through September. Mr. H. Boswell
Lee records one from near Amersham on July 28, 1906, and another near
Wendover in August 1905 (Field, August 4, 1906, p. 239). In 1907 Mr. Oldham
observed ten on Wilstone Reservoir on October 13 and three on October 20. In
1913 he saw one there on October 19, and again on November 2 and November 9,
but these occurrences in October and November are quite exceptional. On
May 4, 1918, about 11 a.m., a party of nine Black Terns and about the same
number of Common Terns with six Black-headed Gulls were seen by Mr. Oldham
at Startops End Reservoir. An hour later, at Wilstone, another party of Terns,
i.e. twelve Black and five Common Terns, were seen flying high in the direction
of the other reservoirs. On returning to Startops End the observer found
thirteen Black and five Common Terns there, probably the party he had seen
over Wilstone at mid-day. On July 21, 1918, he saw an adult bird at Wilstone
Reservoir ; September 8, a young bird about Startops End and Marsworth
Reservoirs. Two were observed by Mr. E. Hollis over Halton Reservoir in the
spring of 1918, probably in May.
196 (417). SANDWICH TERN. Sterna sandvicensis sandvicensis Lath.
Vict. Hist, of Bucks, p. 150.
Rare straggler.
Mr. Heneage Cocks (Zoologist, 1895, p. 190) observed eight adult birds
on the river opposite his house at Great Marlow on April 10, 1895.
244 NOVTTATES ZOOLOGICAE XXVII. 1920.
In October 1886 a pair was shot on the Tring Reservoirs (Vict. Hist, of
Herts, vol. i. p. 214).
197 (419). COMMON TERN. Sterna hirundo hirundo L.
B. of Berks, and Bucks, p. 147. Vict. Hist, of Bucks, p. 151.
Not uncommon on passage.
Seen in spring and autumn, and occasionally at other times of the year,
on all larger sheets of water, especially the Thames and Tring Reservoirs.
Oldham, in litt., writes : " Bird of passage, generally in small numbers,
one to three or four, but occasionally in fair-sized flocks (twenty-eight on May 20,
1910) to mid-June, the latest date being June 15, 1913. Less frequent and never,
in my experience, in large numbers, on return passage from end of first week in
August to mid-September. These birds often stay only for a short time — a few
hours or perhaps only minutes — to rest and feed before passing on. At times
they pass without stopping at all, as Gulls so often do ; for example, on August 8,
1915, three flew over without stopping, going a little S. of W."
198 (420). ARCTIC TERN. Sterna paradisaea Briinn.
B. of Berks, and Bucks, p. 148. Vict. Hist, of Bucks, p. 151.
Rare visitor.
According to Kennedy this Tern is " occasionally seen at the Marsworth
and Wilstone Reservoirs and at other large sheets of water." " Many years
ago Mr. H. Daly shot one of these birds in autumn, near Eton " ; and in Novem-
ber 1865 " an Arctic Tern was obtained at Boveney Locks." Several are also
stated to have been killed near Windsor, and one by Gould near Maidenhead in
May 1866.
An adult female was shot at the Reservoirs by James Street on May 9, 1 893,
and is now in the Tring Museum. The specimen is certainly an Arctic Tern,
though the tip of the bill (in the skin) is blackish, as in Sterna hirundo. One " is
said to have been obtained " in the spring of 1886, but no proof of this exists.
199 (421). LESSER TERN. Sterna albifrons albiirons Pall.
B. of Berks, and Bucks, p. 149. Vict. Hist, of Bucks, p. 151.
Rare, irregular visitor.
In summer and autumn occasionally in small flocks on the Thames, specimens
having been shot near Windsor and Eton, according to Kennedy, who also records
one shot on the canal at Slapton, in May 1850. Adult birds were shot out of
small flocks on the Tring Reservoirs May 8 and 20, 1893.
Near Tring four were observed at Wilstone Reservoir on September 4, 1910,
by Mr. C. Oldham (in litt.).
200 (427). BLACK-HEADED GULL. Larus ridibundus ridibundus L.
B. of Berks, and Bucks, p. 151. Vict. Hist, of Bucks, p. 151.
Common visitor at all seasons.
Not unfrequently seen, chiefly in spring and autumn, but also at other
seasons on the Tring and Halton Reservoirs, along the Thames and on other
Novitates Zoolooicae XXVII. 1920. 245
waters. Mr. Oldham writes (in litt.) : " I have notes of the occurrence in every
month except June. As with other Gulls, parties often pass without alighting
on the waters, but this species often stays for some days, especially in winter,
picking up food on the "banks and mud patches. There seems to be a regular
passage in March and April (a flock of twenty-four at Wilstone Reservoir on
April 29, 1917), and again in August and September. A party of thirty-six
passed over Marsworth and Little Tring Reservoirs on November 4, 1917, but
so large a flock at that time of year is, I think, very unusual."
In the Thames Valley it appears frequently, sometimes in considerable flocks,
especially during floods in spring and autumn. Mr. A. H. Cocks reports flocks of
about fifty or sixty at Skirrnett on April 22nd, 1917, and about forty seen on
plough land near Skirrnett on January 28, 1918.
201 (430). COMMON GULL. Larus canus canus L.
B. of Berks, and Bucks, p. 152. Vict. Hist, of Bucks, p. 151.
Irregular straggler, in fair numbers.
Except Larus ridibundris this is evidently the least rare Gull visiting the
county. It has not infrequently been observed on the Halton and Tring
Reservoirs, and a specimen shot on October 20, 1892, is in the Tring Museum.
Kennedy records it from Chesham, the Thames (near Windsor), Wycombe Rye,
Fawley, and Chalvey (near Slough).
Mr. Oldham writes (in litt.) : " I have notes of this Gull for every month
in the year except June and July. It usually occurs singly or in parties of not
more than half a dozen, but on September 30, 1917, a flock of thirteen immature
birds was observed on Little Tring Reservoir. As a rule the passing Gulls do
not stay on these waters for more than a few minutes, and very often they do not
alight at all. Mature and immature birds are about equally numerous."
In the lower part of the Thames Valley it occurs not uncommonly (E. E.
Petti tt and F. C. R. Jourdain).
202 (431). HERRING-GULL. Larus argentatus argentatus Pontopp.
B. of Berks, and Backs, p. 135. Vict. Hist, of Bucks, p. 151.
Rare visitor.
Clark Kennedy mentions one caught on the river between Maidenhead and
Windsor, January 25, 1855, and several seen between Surley and Eton in the winter
of 1866-7. Among the large Sea-Gulls which now and then, chiefly after fogs
or gales, are observed at the Tring Reservoirs, Herring-Gulls also apparently
occur from time to time, but it is difficult to identify these birds with certainty
at great distances, and no specimen exists in the Tring Museum. Mr. Oldham
writes (in litt.) : " Much less frequent at the reservoirs than Larus canus ; in
fact in eleven years I have only seen the species twice :
" On August 3, 1911, three adults passed over Wilstone Reservoir, without
alighting. Their course was S.W., wind E.
" May 2, 1915, two immature birds passed over Wilstone without alighting."
In the Thames Valley it is not infrequently seen on the wing in small flocks.
246 NOVTTATES ZOOLOOICAE XXVJJ, 1920.
203 (433). LESSER BLACK-BACKED GULL. Larus tuscus affinis Reinh.
Vict. Hist, of Bucks, p. 151.
Bare visitor on migration.
A young female was shot on the Tring Reservoirs by Lord Rothschild on
August 20, 1894. Others are believed to have been seen in winter, but there is
no other specimen to prove this, while Mr. Oldham has never observed the species
in the winter. He says (in lift.) : " Such evidence as I have seems to indicate
a regular passage from S.W. to N.E. in spring, and in the reverse direction in
autumn. These birds, like other Gulls, often drop down to the reservoirs, but
do not alight, and after flying to and fro for a few minutes mount high in the air
and continue their course. On August 30, 1908, a party of thirteen, mostly
adults, dropped down to Little Tring Reservoir, but did not alight. Presently
they soared to a great height, where they joined forces with another party of
twelve, and all drifted away nearly due W., the wind being S.W. On September
4, 1910, a flock of between thirty and forty, mostly adult or nearly so, but a few
brown birds among them, alighted on Wilstone Reservoir. They stayed for
perhaps ten minutes, then rose high and passed away to S.W., the wind being N.
"September 18, 1910, a single adult bird was seen near Marsworth, flying
high in a south-westerly direction.
" May 5, 1912, a party of fourteen adults dropped down to Wilstone Reservoir
but did not alight, then rose high into the air and passed away to N.E., wind E.
"May 20, 1913, a single adult, Wilstone Reservoir.
"August 16, 1914, a single adult passed over reservoirs, going a little W.
of South.
" August 26, 1917, two adults of pale British race, flying S.W., near Wilstone
Reservoir."
An adult male, killed at Bletchley 20. iv. 1910, is in the Bucks County
Museum (E. Hollis, in litt.).
This species, as well as the Herring-Gull, occurs not infrequently on the
wing in the Thames Valley, generally in small flocks (E. E. Pettitt and F. C. R.
Jourdain).
204 (434). GREAT BLACK-BACKED GULL. Larus marinus L.
Vict. Hist, of Bucks, p. 151.
Exceptional straggler.
Lord Rothschild and the keeper, J. Street, believe that they saw this species
on the reservoirs about 1890, but no specimens were obtained. Street also states
he saw four on September 9, 1 897, but no specimen was procured.
205 (437). Kl'lTlWAKE. Rissa tridactyla tridactyla (L.).
B. of Berks, and Bucks, p. 151. Tict. Hist, of Bucks, p. 151.
Rare straggler.
On January 11, 1830, a Kittiwake was killed near Dinton Hall. Kennedy
has recorded it from Datchet, the neighbourhood of Eton, and Chesham. Mr.
A. F. Grossman reports two as shot " at Tring " in January 1885 {Vict. Hist, of
Herts, vol. i. p. 215). Mr. A. H. Cocks reports an adult bird, too weak to fly far,
NOV1TATES ZOOLOQICAE XXVII. 1920. 247
seen by him on the Thames about half a mile above Great Marlow, on February
16, 1894 (in Hit.).
Charles Oldham writes (in lilt.) : " I have no evidence of any regular passage
of this species, and my few notes refer to occurrences in winter, and I think the
birds are storm-driven and always more or less exhausted.
" March 10, 1912, an adult on the bank of Wilstone Reservoir, obviously
in state of exhaustion, and very loth to fly. It was at same place on March 17,
and still reluctant to take wing.
" December 14, 1913, an adult, Little Tring Reservoir.
'; December 20, 1914, an adult at Wilstone Reservoir ; another adult, some
days dead, floating on the water.
" February 14, 1915, an adult on bank at Startops End Reservoir ; almost
too exhausted to fly."
Hartert observed a single adult bird in December 1915, on Wilstone
Reservoir.
200 (440). POMATORHINE SKUA. Stercorarius pomarinus (Temm).
B. of Berks, and Bucks, p. 210. Vict. Hist, of Bucks, p. 151.
Exceptional straggler.
Clark Kennedy writes : "I was informed by Mr. Gardner, of Oxford Street,
that a Skua of this species was sent to them for preservation by a gentleman
resident in Buckinghamshire, on whose estate it was procured. The precise
date, or further particulars, I was unable to ascertain. A second was taken some
years since near Crendon ; and Mr. Burgess told me of a third which was shot at
Chesham, in November or December 1859. This last is in the collection of Mr.
Lowndes."
[A young Skua, probably the Long-tailed Skua, Stercorarius longicaudus
Vieill., stayed several days at the Tring Reservoirs, during the end of August
1919. It was very tame, and was closely observed and photographed by Mr.
Oliver Pike. Being out of its element, it probably perished in some corner. (See
Brit. B. xiii. p. 143).]
207 (445). GUILLEMOT. Uria troiHe troille (L.).
B. of Berks, and Bucks, p. 211. Vict. Hist, of Bucks, p. 151.
Very rare straggler.
G. B. Clarke records a male caught in the river at Fenny Stratford on Novem-
ber 13, 1852 ; another was seen near Simpson on November 14 of the same year
(Morris's Naturalist, 1854, p. 224).
208 (448). LITTLE AUK. Plotus alle (L.)
B. of Berks, and Bucks, p. 212. Vict. Hist, of Bucks, p. 151.
Accidental winter visitor.
Bryant Burgess informed Kennedy that a Little Auk was taken on one of
the reservoirs near Drayton Beauchamp in December 1841. Mr. T. Marshall,
writing to the Standard, December 21, 1901, stated that he knew of another
obtained in Bulstrode Park, Bucks.
248 Novitates Zoolooicae XXVII. 1920.
One was found alive near Newport Pagnell on November 19, 1893 (W. E.
Dawes, Field, December 9, 1893, p. 901).
Edwin Hollis informs us that one was taken alive at Quainton on February
2, 1912, and is now in the possession of Mr. Ashley, of Quainton. He also saw
two others, obtained at Towersey about the same time, while being mounted
at Weston's in Aylesbury. P. W. Horn also records one killed on the Chilterns
near Ivinghoe, on February 4. This was a female, in very poor condition, and
only weighing 3 oz. (Zoologist, 1912, p. 109).
In November 1917 there was another irruption of this species, and several
specimens were picked up in Kent, Sussex, Hants, and on two occasions in Bucks.
On November 11 one was discovered, still living, in Sir Thomas Barlow's garden
near Wendover, but died on the following day ; and another was picked up dead
on the Halton (Weston Turville) Reservoir on November 17, which had evidently
been dead for several da}'s (British Birds, vol. xi. p. 190).
Mr. A. H. Cocks, who has had considerable experience of this species in
Spitsbergen, saw one on the wing on the afternoon of December 8, 1919, at Skir-
mett, near Henley-on-Thames. It was flying westward quite strongly, and
showed no sign of exhaustion. The place where it was observed is about three
miles from the nearest part of the Thames (in litt., December 9 and IS).
209 (449). PUFFIN. Fratercula arctica grabae Brehm.
B. of Berks, and Bucks, p. 212. Vict. Hist, of Bucks, p. 151.
Bare accidental visitor ; four occurrences.
One caught in a ploughed field on the Luton Road, near Aylesbury, after
the great gale of October 14, 1881 (A. Heneage Cocks). H. Howard Vyse (Field,
November 19, 1910, p. 955) records a second, caught at Langley, on November 15.
A third was caught at Oaken Grove, near the Oxford boundary, about
November 19, 1914 (H. Noble, quoted by 0. V. Aplin, Zool. 1915, p. 212).
On November 23, 191S, a female was found between the Waterworks and
Aston Clinton, injured but still alive (E. Hartert, Br. Birds, xii. p. 191).
[LITTLE CRAKE. Porzana parva (Scop.).
A. F. Crossman states on the authority of the Hon. W. Rothschild that
" a specimen is said to have been obtained at one of the Tring Reservoirs on
January 5, 1887 " (Vict. Hist, of Herts, vol. i. p. 212), but the specimen cannot
be traced.]
210 (455). SPOTTED CRAKE. Porzana porzana (L.).
B. of Berks, and Bucks, p. 99. Vict. Hist, of Bucks, p. 148.
Autumn migrant.
This species, living, like many Rails, in the densest vegetation near water
and overgrown ditches, is not easily detected, and may therefore be less rare
than is supposed to be the case, and there is no reason why it should not breed
in Bucks, though no such instance is known to us. On the reservoirs we have
no proof of its occurrence since 1895.
Clark Kennedy records specimens from Surley, Slough, Datchet, High
Wycombe, and West Drayton (on August 27, 1860), as well as twice near Monkey
Novitates Zoolooicae XXVII. 1920. 249
Island on the Thames. The latest occurrence known to us is one from Olney
in November 1897, recorded by Mr. F. Anslow Sole (Field, January 15, 1898, p. 93).
211 (454). LAND-RAIL. Crex crex (L.).
B. of Berks, and Bucks, p. 99. Vict. Hist, of Bucks, p. 147.
Summer resident, now not common.
Arrives during first week of May and stays till September. Kennedy records
a specimen which was picked up in a field on the banks of the Thames, near Eton,
in very poor condition, on Christmas Day 1865. Another is reported as having
been seen and heard (!) on January 25, 1882, between Beaconsfield and Dropmore
(Field, January 28, 1882). Though it is known to occur not infrequently in
winter, especially in Ireland and on the Outer Hebrides, such birds are probably
for some reason unable to migrate, and in most cases are probably doomed, as
the species winters in Africa and cannot live through a northern winter.
In former years it was much commoner in Bucks, though it is even now found
in many suitable localities. Near the reservoirs Oldham and Hartert heard it
in May, June, and July of 1910, 1911, 1913, 1915, 1916, 1917, and 1918.
In the Thames Valley, though formerly very numerous, it has now become
very scarce, only a few pairs breeding here and there. Mr. Pettitt says that
two or three pairs are generally to be met with near Wraysbury, and also a pair
at Medmenham.
212 (459). WATER-RAIL. Rallus aquaticus aquaticus L.
B. of Berks, and Bucks, p. 61. Vict. Hist, of Bucks, p. 148.
Not uncommon winter visitor ; resident in very small numbers.
Clark Kennedy points out that specimens of this species have been obtained
at all times of the year, and that every year a few are killed on the river near
Windsor. He states that the nest has been taken near Eton on more than one
occasion, but gives no details. In the neighbourhood of the reservoirs it occurs
not infrequently in autumn and winter, and specimens have been obtained as
late as April 13, which would seem to point to breeding in the district, though
definite proof is wanting.
We are indebted to Mr. E. E. Pettitt for details of nesting in the Thames
Valley in 1896. On May 26 a man who was cleaning out a large osier bed near
Wraysbury cut out a nest with six eggs, and on June 1 came across a second
nest containing ten somewhat incubated eggs, so that obviously two pairs were
breeding here. Since that time the cover has not been so good and no other nests
have been found. Apart from its very distinctive notes, which, however, are
not familiar to most people, the presence of this secretive species in summer is
not easily detected.
213 (460). MOORHEN. Gallinula chloropus chloropus (L.).
B. of Berks, and Bucks, p. 62. Vict. Hist, of Bucks, vol. i. p. 148.
Common resident, widely distributed.
Very common, even in small ponds in parks and gardens. Their numbers
were considerably diminished after the hard frost in the winter of 1917.
250 NOVTTATES ZOOLOOICAE XXVII. 1920.
214 (461). COOT. Fulica atra atra L.
B. of Berks, and Bucks, p. 61. Vict. Hist, of Bucks, p. vol. i. p. 148.
Fairly numerous resident on inland waters, but rather local.
Common on larger reservoirs, occasionally met with on ponds and still back
waters of rivers. Breeds in great numbers on the Tring and Halton (Weston
Turville) Reservoirs, where their numbers are increased in winter.
In the south of the county Mr. E. E. Pettitt records it as nesting at Horton,
Rickeys Park, and Burnham, but not numerous as a breeding species.
On the Thames it has only been known to nest very rarely. Mr. J. H.
Carpenter recorded an instance of breeding near Marlow in 1899 (cf. Field,
September 9, 1899) : and on May 12, 1919, Mr. E. E. Pettitt found a nest
with seven eggs on the river between Marlow and Henley.
[CAPERCAILLIE. Tetrao urogallus urogallus L.
B. of Berks, and Bucks, p. 182. Vict. Hist, of Bucte. vol. i. p. 147.
According to Kennedy, " in the autumn of 1855 a cock and hen were shot
in the woods known as Burnham Beeches." The author concluded that it was
most unlikely that they were " visitors from Scandinavia," and almost equally
so that they could have flown from Scotland, so " that they must have escaped
from confinement." Unfortunately the latter seems equally improbable, as
Capercaillie are not usually kept in confinement.]
215 (463). BLACK GROUSE. Lyrurus tetrix britannicus With, and Lonnb.
B. of Berks, and Bucks, p. 5(5. Fi-ld, vol. xxii. 1863, p. 297. Vict. Hist, of Bucks, vol. i. p. 147.
Rare straggler or introduced ?
Clark Kennedy informs us that five Black Grouse from Holland were turned
out in 1815 on Hurtwood Heath between Dorking and Guildford in Surrey.and that
some of the descendants of these birds strayed as far as Finchhampstead in Berk-
shire, and that they bred near Windsor, where some were also turned out a few
years before 1868, but that " many have immigrated and are now located on Ascot
Heath, Woking Common, Bagshot Heath, and other suitable localities." He
also says that " a good many brace " were shot in 1867 in Berkshire, further that
the last which came under his notice was a fine male killed on Hyde Heath, near
Chesham, in 1852, and that this bird was then in the collection of Captain Fuller.
In the Field, September 19, 1863, vol. xxii. p. 197, is the following letter : " Lord
Curzon presents his compliments to the Editor of the Field, and begs to inform
him that his keeper shot a very fine Blackcock in the woods near Penn House,
Amersham. Lord Curzon is quite unaware from whence this bird could have
come ; he has been seen during the summer, and has been sent to the Earl Howe,
at Gopsall, near Atherstone." Unfortunately Kennedy did not explain how it
was ascertained that " many immigrated " into Berkshire, and it is now impossible
to ascertain whether the Bucks. Blackcocks, shot near Chesham and Amersham,
were descendants of the introduced stock or stray birds from elsewhere. If
introduced from Holland they would be Lyrurus tetrix tetrix, if indigenous L.
tetrix britannicus With, and Lonnberg (cf. Brit. B. vol. vi. p. 270). Kennedy's
Novitates Zoolooicae XXVII. 1920. 251
statement that Blackgame were introduced from Holland is quite correct, but
they were also indigenous in Surrey, and were present hundreds of years before
any were introduced.
216 (466). PHEASANT. Phasianus colchicus L.
B. of Berks, and Bucks, p. 56. Vict. Hist, of Bucks, vol. i. p. 147.
Common in wooded districts and parks.
Phasianus colchicus colchicus was introduced about 900 years ago, but it is
now generally hybridized with P. colchicus torquatus, which was introduced about
200 years ago and later. It is common in all wooded parts and parks of the
county. Other subspecies of P. colchicus have also been introduced recently,
and in addition P. versicolor has been turned down, and these birds have to some
extent hybridized with the old stock.
217 (467). COMMON PARTRIDGE. Perdix perdix perdix (L.).
B. of Berks, and Bucks, p. 57. Vict. Hist, of Bucks, vol. i. p. 147.
Numerous resident.
Common everywhere in suitable localities.
218 (469). RED-LEGGED PARTRIDGE. Alectoris rufa rufa (L.).
B. of Berks, and Bucks, p. 57. Vict. Hist, of Bucks, vol. i. p. 147.
Now locally common.
Clark Kennedy said that the Red-leg was introduced into Windsor Park
in the reign of King Charles II, but that all the descendants of the old stock are
supposed to have perished. A century later it was successfully reintroduced
into Suffolk, and subsequently into many other places, and is now well established
in all midland and southern counties. It is now locally common in the county,
though nowhere as numerous as the Common Partridge. " J. C. S. P.," in the
Field, October 7, 1865, p. 256, reports four killed near Bicester in 1865, adding
that he never heard of any before in the district. It is generally more fond of
dry ground than of low-lying meadows, but this is not the case everywhere. Mr.
A. H. Cocks remarks that when he first came to Skirmett quite half the stock of
Partridges were Red-legged birds, but that since then the proportion of Grey
Partridges has greatly increased, while the Red-legs have almost disappeared.
In 1899 Mr. J. P. Athawes found a nest of this species with sixteen eggs on a
straw-stack 18 feet from the ground at Loughton, near Bletchley (Field, July 22,
1899, p. 178).
219 (468). QUAIL. Cotumix coturnix coturnix (L.).
B. of Berks, and Bucks, p. 138. Vict. Hist, of Bucks, vol. i. p. 147.
Now very rare summer resident.
Formerly not rare, though even in 1868 Kennedy called it " not common."
He then said that " the majority of the Quails which are obtained in Berkshire
and Buckinghamshire are shot either- in May or September." The shooting in
May must have had a disastrous effect and is a thing almost incredible at the
present time. In the Vale of Aylesbury Quails used to be fairly common about
252 NOVTTATES ZOOLOOICAE XXVII. 1920.
half a century ago, and a few were seen and occasionally shot in September
near the boundaries of Herts, until twenty-five or twenty-six years ago. Since
then Hartert has only at long intervals heard Quails calling in the summer near
Cheddington, Leighton Buzzard, and Ivinghoe. Mr. Oldham heard one in a field
of oats at the foot of Ivinghoe Beacon on July 14, 1917. The same observer
heard one calling in a field of growing corn close to Wilstone Reservoir, near
Tring, May 25, 1919, and again in a field of oats at the foot of Ivinghoe Beacon,
June 29 of the same year. At the foot of this Beacon a few Quails were met
with when shooting about thirty years ago, as Hartert was told by Mr. A. W.
Vaisey.
[The Rufous Tinamou mentioned by Allen as seen near Olney in Bucks.
(Field, 1902, p. 288) was of course an escaped or introduced specimen.]
NOVITATES ZOOLOGICAE XXVII. 1920. 253
AN ORNITHOLOGICAL BIBLIOGRAPHY OF BUCKINGHAMSHIRE AND THE
TRING RESERVOIRS
By the Rev. F. C. R. Jouedain, M.A., M.B.O.U., etc.
1827. Yabbell, W. Little Bittern [near Windsor] (Zool. Journ. 1827, p. 88).
1831.. Tatem, J. G. The Kingfisher [near Loudwater and Woodburn] (Mag. Nat.
Hist. [Loudon's], iv. p. 267).
1837. Blyth, E. Notes on the Pern, or Honey Buzzard [breeding at Burnham
Beeches teste Gould] (Mag. Nat. Hist. [Charlesworth], 2nd %, i. p. 536-41,
partim) .
1848. Crewe, H. H. White variety of the Hedge-Sparrow (Sylvia modularis) [near
Tring] (Zool. p. 2143).
1849. Crewe, H. H. Occurrence of the Hawfinch at Tring [at Drayton in April] (Zool.
p. 2454).
,, [Gould, J.] British Distribution of Motacilla boarula (Contrib. to Ornith.
1849, p. 137) [breeding at Chenies].
„ Williams, Rev. J. Occurrence of the Bearded Tit (Parns biarmicus) near
Tring [Pair shot at Reservoirs, 21. xii. 48] (Zool. p. 2418).
,, Occurrence of the Garganey (Anas querqvedula) near Tring [seven obtained
at Reservoirs, 24. iii. 49] (t.c. p. 2421).
,, Occurrence of the Goldeneye (Anas clangula) at Tring [male shot on
Reservoirs early in 1849] (t.c. p. 2421).
1854. Claeke, G. B. Guillemot at Fenny Stratford, Bucks. (Nat. [Morris's]).
1859. Body, R. B. The Hoopoe [seen by Hon. G. F. Berkeley at West Wycombe]
(Field, May 7, p. 364).
„ Ingatton, T. The Hoopoe [one wounded and caught Burnham Gore, May 3]
(t.c, loc. cit.).
„ Owen, J. W. The Egyptian Goose [shot at Marlow, November 1] (t.c. Novem-
ber 19, p. 424).
1861 . Hassell, G. Hoopers shot in Buckinghamshire [two at Wragsbury (= Wrays-
bury), January 17] (Field, February 2, p. 93), Idem (Zool. p. 7385).
„ " H. M. L." Sea-Swallows on the Thames [above Boveney Lock] (t.c. May 25,
p. 451).
„ C W[olley]. Eggs of the Golden Oriole [taken near Stoke : afterwards
proved to be Song-Thrush's] (t.c, loc. cit. and August 3).
1862. Crewe, H. H. [Letters on Dotterel and Cirl-Bunting in Bucks.] (Ibis, pp. 390-1 ).
Jones, H. J. The Hoopoe [female shot Stewkley, April 24] (Field, May 3, p. 387).
,, Willis, T. Osprey shot near Windsor [at Ditton Park] (t.c. October 4,
p. 319).
1863. Curzon [Visct.]. Blackcock in Bucks, [near Amersham] (Field, September 19,
p. 297).
1864. Crewe, H. H. Osprey, Great Grey Shrike, and Cirl-Bunting in Herts, and
Bucks, (op. cit. December 3, p. 384).
" F. W." Late Martin [on November 22] (Field, Xovember 26, p. 378).
„ Tyeee, R. Bramblings in the Chilterns (Zool. p. 9023) ; Idem by H. H. Crewe
(t.c. p. 9109).
,, Tyrer, R., Jiin. A Yellow Skylark ; Hawfinch at Weston Turville (t.c.
p. 8950).
1865. Botting, W. B. Northern Diver in Buckinghamshire [on the Thames] (Field,
December 9, p. 426).
254 NOV1TATES ZOOLOGICAE XXVII. 1920.
1865. Crewe, H. H. [Letter on Ospreys and Cirl- Bunting in Bucks.] (Ibis, p. 113).
„ Osprey in Bucks, and Hertfordshire and Great Grey Shrike and Cirl-Bunt-
ing in Bucks, [two Ospreys at Wilstone Reservoir, September 1864 ; Cirl-
Bunting breeding] (Zool. p. 9415).
„ T. M[arshall]. Occurrence of a Little Bittern on the Thames [near Maiden-
head] (Field, October 7, p. 254).
,, " J. C. S. P." French Partridges in Bucks, (t.c. October 7, p. 256).
1866. Marshall, T. Martins (Quart. Mag. High Wycombe N.H. Soc. p. 26).
1867. Clifton, Lord. Savi's Warbler (?), Plover and Lesser Spotted Woodpecker
in Bucks. (Zool. p. 704) ; A Strange Trap for Swallows (p. 990).
,, Gardner, J. Honey-Buzzard [near Maidenhead, Berks.] (Field, July 27, p. 73).
,, Kennedy, A. Clark. Ornithological Notes from Buckinghamshire (Zool.
p. 637) ; Siskin in Bucks (p. 705) ; Curious Fact connected with the Bramb-
ling (p. 706) ; Early Arrival of Swallows and Martins (p. 827) ; Instinct
in the Swan (p. 916) ; Dates of the Departure of Immigrants for 1867 (p.
1015) ; Lesser Spotted Woodpecker near Windsor (p. 1016).
„ Marshall, T. The Green Woodpecker (Quart. Mag. High Wycombe N.H.S.
No. iii. p. 73) ; White Sand-Martin ; The Wheatear (t.c. No. vi. p. 146).
,, Ullyett, H. List of Wycombe Birds, No. 1 (t.c. No. iii. p. 68).
1867-9. Sharpe, R. B. The Birds of Cookham, 8 pts. [unfinished] (op. cit. October
1867 to July 1869) [partim].
1868. Clefton, Lord. Wood-Lark [seen in January at Eton] (Zool. p. 1132).
,, Crewe, H. H. Scarcity of the Redwing (t.c. p. 1177).
,, Kennedy, A. Clark. The Birds of Berkshire and Buckinghamshire, a Contri-
bution to the Natural History of the two Counties, post 8vo, pp. xvi, 232, ill.
Eton and London.
„ Swallows in November (Zool. p. 1058) ; Storm-Petrel in Buckinghamshire
(t.c. p. 1178) ; Note on the Breeding of the Bittern in Buckinghamshire (t.c.
p. 1255).
„ Marshall, T. Late Martins (Quart. Mag. High Wycombe N.H.S. No. vii.
p. 170).
,, Newman, E. [Review of the Birds of Berks, and Bucks.] (Zool. p. 1243).
1869. Bowstead, R. M. The Sparrow-Hawk and the Kestrel (Quart. Mag. High
Wycombe N.H.S. p. 72).
„ Marshall, T. The Common Buzzard [breeding in Bucks] (I.e. p. 71).
„ " R. S." Late Hirundines [House- Martin, November 20; near Eton] (Field,
November 27, p. 458).
1870. Williamson, J. W. Wild Swans in Buckinghamshire [evidently C. olor]
(Field, January 1, p. 9) ; Idem by " Berea " (t.c. January 8, p. 30).
1871. " Harry L." Quails in Britain in 1870 [in Bucks.] (Field, January 28, p. 70).
„ Mackenzie, W. D. Nests imbedded in Trees [Sparrow's nest in 8-9 in. timber]
(t.c. June 3, p. 443).
,, " Sept." Wild Swans near Thame [between Thame and Shabbington] (t.c.
February 11, p. 108).
1872. Harting, J. E. British Heronries [partim] (Zool. p. 3261) ; cf. also Idem by
H. Burney (op. cit. 1873, p. 3651) ; Supposed Occurrence of Wilson's Snipe
in Cornwall [and Bucks.] (Zool. p. 3273).
1873. Cocks, A. H. Notes from Berks, and Bucks. [Montagu's Harrier, Redwing,
etc.] (Field, February 8, p. 135).
1874. Crewe, H. H. House-Martin [near Aylesbury on December 5] (Zool. p. 3833).
,, "Head Keeper." Moorhen's Nest in Tree (Field, May 30, p. 524).
1875. Marshall, T. Buzzards in Bucks, [at High Wycombe, etc.] (Field, March 2,
p. 272).
Novitates Zoolooicae XXVII. 1920. 255
1876. Dod, C. W. Arrival of Summer Birds [Wryneck, April 2, at Eton] (Field,
April 8, p. 414).
„ " J. L. H." Late Martins [November 16] (Sci. Gossip, p. 23).
„ Macmeikan, J. Arrival of Summer Migrants [Nightingale, March 29, 1874]
(t.c. April 22, p. 464).
„ Prior, C. M. Crow laying twice in the same Nest [and three birds to nest]
(Zool. p. 5005).
1877. Thurlow, J. Storm-Petrel driven Inland [High Wycombe, one seen] (Field,
October 20, p. 441).
1878. Blake, V. Arrival of Wryneck [at Slough] (Field, April 13, p. 453).
„ Cocks, A. H. Provincial Names in Berks, and Bucks. (Zool. p. 334).
,, Crewe, H. H. Albino Specimens of the Common Snipe and Wryneck (t.c.
p. 29).
1879. Curtis, E. Scoter on the Thames [near Windsor] (Field, March 29, p. 369),
Idem (Zool. p. 220) ; Rare Birds in Berks. [Sheldrake on Thames] (Field,
December 27, p. 853).
„ White, H. Golden Oriole in Buckinghamshire [at Stoke Mandeville] (t.c.
May 31, p. 625).
1880. Burney, H. Siskin nesting in Beds, [errore Bucks.] (Zool. p. 259) ; Idem by
R. H. Mitford (t.c. p. 364 ; cf. Vict. Hist, of Beds. i. p. 112).
,, [Editorial] Dr. Lamb's " Ornithologia Bercheria " (Zool. pp. 313-25) [partim].
Marshall, T. Rough-legged Buzzard in Bucks. [High Wycombe] (Field.,
December 18, p. 905).
1881. Crewe, H. H. Storm-Petrel near Wendover (Zool. p. 68).
Hartlng, J. E. Food of the Wood-Pigeon (Field, November 5, p. 678).
1882. Aplin, F.C. Honey-Buzzards in Bucks, [near Brill in September] (Zool. p. 116).
,, " Korax." Corncrake calling in January [near Beaconsfield] (Field, January
28, p. 129).
1883. Crewe, G. A. Scaup-Duck inland [near Tray ton Beauchamp] (Field, December
15, p. 809).
,, Hibbert, L. Osprey shot near Slough [in Chalfont Park] (t.c. October 6,
p. 490).
,, Travis, T. Arrival of Waxwings [partim] (t.c. January 27, p. 131).
1884. Aplin, F. C. Grey Form of Tawny Owl in Bucks. (Zool. p. 471).
1888. Littleboy, J. E. Notes on Birds observed in Herts, during 1886 [with Notes
on Reservoirs] (Trans. Herts. Nat. Hist. Soc. iv. pp. 161-8).
,, Lilford, Lord. Magpies attacking a Weakly Donkey [at Doddershall Park]
(Zool. p. 184).
,, Marshall, T. Crossbills in Bucks, [at Hughenden] (Field, December 29,
p. 951).
,, Odling, E. C. Hoopoe in Bucks, [at Wendover] (t.c. April 14, p. 536).
,, Parrott, F. H. Starling Nesting in November [at Aylesbury] (Zool. p. 33).
1 889 . Aplin , O . V . The Birds of Oxfordshire , pp . viii , 2 1 7 , 8vo , Oxford , 1 889 [partim] .
„ Tomalin, W. Hoopoe in Buckinghamshire [Lavender Park Farm] (Field,
November 30, p. 777).
1890. Aplin, O. V. On Distribution and Period of Sojourn in British Isles of the
Spotted Crake [partim] (Zool. p. 407).
„ Knapp, J. M. Velvet Scoter Inland [at Linfield] (Field, November 1, p. 668).
,, Littleboy, J. E. Notes on Birds observed in Hertfordshire in 1887, and on
the Birds frequenting the Tring Reservoirs (Trans. Herts. Nat. Hist. Soc.
v. 1887-9, pp. 76-88).
„ Vyse, H. H. Unspotted Eggs of the Spotted Flycatcher (Field, August 16,
p. 250, and Zool. p. 352).
256 • NOVITATES ZOOLOGICAE XXVII. 1920.
1891. Cocks, A. H. Smews in Bucks, and Oxon. (Zool. p. 153) ; Destruction of King-
fishers (t.c. p. 154).
„ Marshall, T. Bee- Eater in Leicestershire [and Golden Oriole near Aylesbury,
1880] (Field, May 16, p. 738).
1892. Aplin.O. V. On the Distribution of the (irl- Bunting in Great Britain [partim]
(Zool. p. 174).
„ Vyse, H. H. Ruddy Sheldrake in Bucks, [reared in captivity] (t.c. p. 359).
„ Yottng, J. Reminiscences of the Kite in Bucks, (t.c. p. 232).
1893. Dawes, W. J. Little Auk Inland [near Newport Pagnell] (Field, December 9,
p. 901).
1894. Aplin, O. V. Whimbrel in the Midlands [in N.-W. Bucks in May] (Zool. p.
266).
Baknett, C. J. Little Owl in Bucks, [at Turville] (Field, May 26, p. 735).
,, Lewis, H. Notes on Birds observed in Herts, during 1892 [incl. Reservoirs]
(Trans. Herts. Nat. Hist. Soc. vii. pp. 161-7).
„ Marshall, T. Hawfinches in Bucks, (t.c. January 27, p. 127).
1894-5. Rothschild, Hon. W. The White Swallows of Aylesbury (Novitates Zoolo-
gicae,\. p. 667, and ii. p. 484).
1895. Cocks, A. H. Sandwich-Terns on the Upper Thames [Great Marlow] (Zool.
p. 190).
1896. Lewis, H. Notes on Birds observed in Herts, during 1894 [with Notes on
Reservoirs] (Trans. Herts. Nat. Hist. Soc. viii. pp. 147-52).
1897. De Castro, D. Terns on the Thames [Magna Charta I.] (Field, August 14,
p. 307).
„ Marshall, T. Little Owl [at Fingest] in Bucks, (t.c. January 30, p. 135).
,, Walshe, P. Great Plover in Bucks. (Nat. Joum.). (Not seen.)
1898. A. A[llen]. Californian Quail in Bucks, [at Newport Pagnell] (Field, January
22, p. 124).
„ Crossman, A. F. Notes on Birds observed in Herts, during 1896 [with Notes
on Reservoirs!] (Trans. Herts. Nat. Hist. Soc. 1898, pp. 148-60).
„ Marshall, T. Crossbills in Bucks, [between Penn and Wycombe] (t.c.
December 3, p. 897) ; Dipper in Hants, [also in Bucks. 1894] (loc. at.).
„ Sole, F. Anslow. Spotted Crake in Bucks, [at Olney] (t.c. January 15,
p. 93).
1899. Athawes, J. P. Partridge's Nest in Straw-stack [at Loughton] (Field, July
22, p. 178).
„ Carpenter, J. H. Coots on the Thames [near Marlow] (Field, September 9,
p. 478).
„ Reid, Sm H. Rae. NighVHeron in Bucks, [at Taplow] (t.c. August 26, p. 394) .
„ Webb, W. M. A Guide to the Museum of Eton College [Appendix, List of Birds,
pp. i-iv], Eton College, 1899.
1901. Crossman, A. F. Notes on Birds observed in Herts, during 1897 (Trans. Herts.
Nat. Hist. Soc. x. pp. 33-43, during 1898 pp. 84-102) [Reservoirs!].
„ A List of the Birds of Hertfordshire [many notes on Reservoirs] (t.c.
pp. 84-102).
„ Marshall, T. The Little Auk [in Bulstrode Park, Bucks.] (Standard, Decem-
ber 21).
„ Rothschild, Hon. N.C. [Exhibition of Baer's Pochard shot at Tring, November
1901] (Bull. B.O.C. xii. p. 25) (cf. H. Saunders, Brit. Birds (Mag.), i. p. 14,
and Hon. W. Rothschild, t.c p. 63).
1902. Allen, A. Rufous Tinamu in Bucks, [near Olney] (Field, March 1, p. 288).
1903. Aplin, O. V. Notes on Oxfordshire Ornithology by the late C. E. Stubbs
[partim] (Zool. pp. 444-53).
N0V1TATES ZoOLOGICAE XXVII. 1920. 257
1903. Emson, C. H. Snow-Bunting on Chiltern Hills [on Ivinghoe Beacon] (Field,
November 14, p. 844).
,, Crossman. Notes on Birds observed in Herts. during 1900 [Reservoirs!] (Trans.
Herts. Nat. Hist. Soc. xi. pp. 47-52).
1904. Cocks, A. H. Birds of Oxfordshire or Buckinghamshire ? (Zool. p. 34) ; Idem,
by O. V. Aplin(<.c. p. 75).
1905. Habtebt, E., and Rothschild, Hon. W. Birds [of Bucks.] (Victoria History
of County of Bucks, i. pp. 128-52 ; 4to, London.
1906. Bickbeton. Notes on Birds observed in Herts, during 1903 [Reservoirs!]
(Trans. Herts. Nat. Hist. Soc. xii. pp. 125-33).
„ Durham, E. B. Bramblings in Bucks, [at Chesham Bois] (Field, December 1,
p. 948).
„ Farwell, W. Bramblings nocking in Winter [at Burnham Beeches] (t.c.
February 3, p. 182).
„ Kerr, G. W. The Birds of the District of Staines, four papers [partim] (Zool.
pp. 179-84, 230-4, 307-10, 386-9).
,, Lee, H. Boswell. Black Tern near Amersham (Field, August 4, p. 239).
„ Macpherson, A. H. Late Singing of Willow- Warbler [in August] (i.e. August
25, p. 342).
„ Noble, H. Birds [of Berks.] (Victoria History of Berkshire, i. pp. 140-66),
4to. London. [Partim.]
1907. "M. L." Bittern near Eton (Field, March 9, p. 394).
„ Mackenzie, W. D. Peregrine Falcon in Oxfordshire [in Fawley Park] (Field,
February 23, p. 307).
1908. Bickerton , Notes on Birds observed in Herts, during 1905 [Reservoirs] (Trans.
Herts. Nat. Hist. Soc. xiii. pp. 49-63).
„ Crouch, L. W. Large Clutch of Eggs of the Great Crested Grebe [seven eggs]
(Brit. Birds, i. p. 327).
Keer,G. W. The Birds of the District of Staines (Zool. pp. 137-43).
,, Monckton, F. A. Corn-Bunting singing in November [near Eton] (Field,
November 14, p. 888).
„ Proctor, Majob F. W. The Lesser Redpoll as a Breeding Species in Berks.
[partim] (Brit. Birds, i. p. 312).
,, Vyse, H. H. Stone-Curlew in November [at Burnham Beeches] (Field, Novem-
ber 14, p. 888).
1909. "J. T. A." Summer Birds in North Bucks. (Field, May 1, p. 763) ; Scarcity
of Nightingales (t.c. May 22, p. 890).
,, Kebe, G. W. Marsh-Warbler [breeding] in Bucks. (Zool. p. 397) ; cf. Brit.
Birds, hi. p. 232.
,, Rothschild, Hon. L. W. Unusual Birds in Hertfordshire [Long-tailed Duck,
Pallas' Sand-Grouse, etc.] [partim] (Brit. Birds, ii. p. 309).
,, Smith, J. Beddall. Irruption of Crossbills [Bucks.] (op. cit. iii. p. 228).
,, Vaughan, H. Green Sandpiper in Bucks, in January (Field, January 23,
p. 157).
1910. Noble, H. Irruption of Crossbills [Bucks.] (Brit. Birds, iii. p. 303) ; Idem by
C. Oldham (t.c. p. 409).
„ Oldham, C. Common Scoter and other Ducks in Herts, and Bucks, (t.c.
iii. p. 414).
„ Vyse, H. H. Puffin taken in Bucks, [at Langley] (Field, November 19,
p. 955).
1911. Allen, A. Little Bittern in Bucks, [near Olney] (Field, August 19, p. 474) ; .
The Great Shearwater Inland [P. major killed by telegraph wires at Olney]
(t.c. October 28, 968).
17
258 NOVITATES ZOOLOGICAE XXVII. 1920.
1911. Aplln, 0. V. Peregrine Falcon in the S. Midlands [near Buckingham] (Zool.
pp. 7-8).
"H. M. B." Arrival of the Wryneck [March 13, Eton] (Field, March 18,
p. 538).
,, De Grdchy, G. F. B. Supposed Occurrence of the Whinchat in Winter [? Stone-
chat] (i.e. February 4, p. 230).
,, Hollis, E. Nutcracker in Bucks [near Aylesbury] (Zool. p. 386) ; Nutcracker
near Aylesbury (Field, October 14, p. 877) ; Slender-billed Nutcracker in
Bucks. (Brit. Birds, v. p. 167).
,, Vyse, H. H. Hen-Harrier and Little Owl in Bucks, [at Langley and Fulraer]
(Field, December 2 and 23, pp. 1234 and 1394) ; Idem by A. H. Cocks,
" R. B. B.," and " Rara Avis " (I.e. December 9 and 16, pp. 1289, 1350).
1912. Bulstkode, R. Crossbill nesting in Bucks, [at Gerrards Cross, 1910] (Brit.
Birds, vi. p. 60).
„ Bickerton, W. Notes on Birds observed in Herts, during 1908 and 1909
[Reservoirs] (Trans. Herts. Nat. Hist. Soc. xiv. pp. 97-111 and 193-206).
Horn, P. W. Little Auk [in Bucks.] (Zool. p. 109) ; cf. Brit. Birds, v. p. 311.
1913. Baynes, G. K. Blackcap ... in England in Winter [at Bourne End, Decem-
ber 29] (Brit. Birds, vi. p. 279).
,, Dowson, E. M. Buzzard at Stoke Poges (Field, April 19, p. 772).
„ Dukham, E. B. Redwing in September [at Chesham Bois] (t.c. September 27,
p. 681).
,, Oldham, C. Red-necked Grebe in Hertfordshire [twice seen on Reservoirs,
1910 and 1913] (Brit. Birds, vi. p. 374) ; Common Scoters in Summer in
Hertfordshire and Buckinghamshire [Reservoirs, July] (t.c. vii. p. 119).
„ Steele-Elliott, J. Hobby in Bucks, [at Lavendon] (Zool. p. 465).
1914. Cocks, A. H. Stone-Curlew breeding in Buckinghamshire (Brit. Birds, viii.
p. 173).
,, Hollis, E. Stone-Curlew breeding in Buckinghamshire [on Chilterns] (t.c.
viii. p. 121).
,, Noble, H. Stone-Curlew breeding in Buckinghamshire [near Fawley Court]
(t.c. viii. p. 173).
,, Rothschild, Hon. W. Kite in Buckinghamshire [near Wendover, December
1913] (op. cit. vii. p. 299).
1915. Bickerton, W. Notes on Birds observed in Herts, during 1912 and 1913
[incl. Reservoirs!] (Trans. Herts. Nat. Hist. Soc. xv. pp. 155-66, 209-22).
,, Hartert, E. Early Nesting of Reed- Warbler [May 16] (Brit. Birds, ix. p. 48).
,, Hetherlnoton, W. C. Infertile Eggs in Nests of Whitethroat (t.c. p. 71).
,, Oldham, C. Black Redstart in Hertfordshire [by Tring Reservoir] ((.e. ,
p. 185).
1916. Cocks, A. H. Snowy Owl in Bucks, [in July 1912] (Zool. p. 313 ; cf. Brit.
Birds, x. p. 122) ; Yellow-hammer's Nest in Rick (Zool. p. 352) ; House-
Martins and House- Sparrows (t.c. p. 357).
Gazeley.H.S. The Pochard in Bucks. (Wild Life, viii. p. 162).
„ Hannett, C. E. J. [Letter on Breeding of Hoopoe at Taplow] (Selborne Mag.
p. 98) ; cf . Brit. Birds, x. p. 122.
>, ,, Kerr, G. W. The Lesser Redpoll in the Thames Valley (Wild Life, viii. p. 94).
„ Pettitt, E. E. One Cuckoo — and others [eleven eggs from one female in a
season] (Wild Life, vii. pp. 56-60, 92- 7).
1917. Bickerton, W. Notes on Birds observed in Herts, during 1914 and 1915
[incl. Reservoirs !] (Trans. Herts. Nat. Hist. Soc. xvi. pp. 93-105, 141-54).
,, Cocks, A. H. Black-headed Gulls in Bucks [at Skirmett, April] (Field, May 5,
p. 663).
NOVITATES ZOOLOGICAE, Vol. XXVII, I92O.
Pi.. XII.
riwt. tr O. C. Pike.
Grasshopper-Warbler feeding young, Marsworth Reservoir.
'
NOVITATES ZOOLOGICAE, Vol.. XXVII, [020
1Y. XIII.
Phut, ty <>. G. Pike
Black-necked Grebe on nest, Marsworth lieservoir.
NOVTTATES ZOOLOOICAE XXVII. 1920. 259
1917. Oldham, C. Blue-headed Wagtail in Hertfordshire [at Tring Reservoirs] (Brit.
Birds, xi. p. 20).
„ Pettitt, E. E. Blue Eggs of Spotted Flycatcher ; Late Breeding of Dabchick
{Wild Life, ix. pp. 12, 267) ; two notes.
„ Priestley, R. C. Wrynecks [nesting notes at High Wycombe] (t.c. p. 268).
1918. Jourdain, Rev. F. C. R. Little Auks in Kent, Sussex, Bucks. ... etc
[two occurrences, November 1917] (Brit. Birds, xi. p. 190).
,, Oldham, C. [On the Breeding of the Black-necked Grebe on the Tring Re-
servoirs] (Bull. B.O.C. xxxix. pp. 28-34).
,, Dusky Redshanks in Hertfordshire [Tring Reservoirs, August 25] (Brit.
Birds, xii. p. 117).
1919. [Editors.] Breeding of the Black-necked Grebe in Hertfordshire (Brit. Birds,
xii. pp. 211-13).
,, Hartert, Dr. E. Puffin in Buckinghamshire [near Aston Clinton] (t.c.
p. 191).
,, Mayall, A. Large Clutches of Chaffinch's Eggs (t.c. p. 80).
,, Pike, Oliver G. The Black-necked Grebe a new Nesting Bird for England
[with nine excellent photos, taken on Tring Reservoirs] (Country Life,
xlvii. pp. 293-7, September 6, 1919).
„ The Black-necked Grebe [on the Tring Reservoirs], with seven plates
(Brit. Birds, xiii. pp. 146-54).
,, Probable Long-tailed Skua in Hertfordshire [on Tring Reservoirs] (Brit.
Birds, xiii. p. 143).
1920. Cocks, A. Heneage. Little Auk in Buckinghamshire [seen at Skirmett,
December 8] (Brit. Birds xiii. p. 246).
2(,Q NOVTTATES ZOOLOGICAE XXVII. 1920.
SOME AFRICAN ANTHRIBIDAE.
By Dr. Karl Jordan.
1. Mecocerus albiceps spec. nov.
$. M. fasciculate Kolbe (1S95) subsimilis, rostro cum capite vitta alba
signato, elytris area albo tessellata dorsali communi magna in medio valde
constricta. Rostrum latum deplanatum, dorso bicarinatum, basi sulco brevi
mediano instructum. Pronotum sparsim granulatum ; carina dorsali recta in
medio levissime interrupts, versus latera angulata, carina laterali alta. Elytra
pone basin gibbosa, seriatim punctata, striis 1* et 2" parum impressis.
Long. 12 mm. ; lat. 5'5 mm.
Hob. Nguelo, Usambara ; 1 $.
In the style of colouring the species agrees with Physopterus melanoleucvs
Jord. (1913). The rostrum is broad, and bears dorsally on each side of the
flattened median area a rather broad carina which is slightly bent outward in
the middle and is distant from eye. At the base there is a short median groove,
and another shorter and more rounded groove is situated beyond the centre,
where the carina* widen and disappear ; between the second groove and the
apical margin a slight median carina ; between the dorsal carina and the raised
edge of the antennal groove the rostrum is impressed, but there is no sulcus
along the carina. Frons broad, being anteriorly at its narrowest point half as
broad as the rostrum is long, measured in the middle. The occiput brown, the
white stripe tripartite. Antenna pubescent white, club with the exception of
the base of segment 9 rufous brown ; segment II much shorter than III
(measurements 7 and 10), IX in length like III, VIII and X like II, and XI a
little longer than X.
Pronotum much rubbed, with indications of an ochraceous median vitta ;
at the sides a large basal ochraceous spot ; laterally and along the carina dispersed
granules, on the disc a shallow depression ; carina with a small forward angle
nearer the sides than middle ; lateral carina very prominent in dorsal aspect.
Elytra with the base very distinctly marginate ; a large patch of white spots
extends from the subbasal humps to the beginning of the apical declivity, in
middle confined to the sutural interspace, anteriorly reaching to the third row
and posteriorly to the fifth ; a white spot above shoulder and a few dots here
and there ; the rows of punctures not impressed, with the exception of the first
and second ; base and sides spotted with ochraceous.
Pubescence of underside greyish white, side of metasternite ochraceous. tip
of metepimerum white ; mesosternal process broader than long. Tibiae rufous
brown, grey near base and beyond middle ; first and last tarsal segments grey
with rufous-brown tips, second segment with few grey hair-scales ; first foretarsal
segment longer than fourth.
'2. Mecocerus balteatus spec. nov.
$. Niger, subtiliter brunneo pubescens ; elytris, metasterno abdomineque
pube cinerea densissime tectis, balteo lato nigro cinctis.
Hab. Benito, Spanish Guinea ; 1 ?.
NOVITATES ZOOLOGICAE XXVII. 1920. 261
Near M. oculatus Jord. (1895).
Head, rostrum, upper- and underside of prothorax, the extreme base of the
elytra, mesosternum, apex of metasternum, and base of first abdominal sternite
black clothed with a mummy-brown pubescence which does not conceal the
dark colour of the derm ; rest of body covered with a dense ashy-grey pubescence
which has a faint luteous tint ; on the elytra a transverse black band, 3'5 mm.
wide near suture, narrowing at the sides, continuous with the transverse band
of the underside, slightly brownish in sutural half ; the narrow basal band
widened at the shoulders. Legs black, with thin grey pubescence, which is
denser on the tarsi.
3. Mecocerus de missus spec. nov.
?. Niger, omnino schistaceo-griseo pubescens, elytris fascia transversa nigra
notatis.
Hab. Gaboon (A. Moequerys), 1 $, type ; Benito, Spanish Guinea, 1 $.
Likewise a near ally of M. oculatus.
Uniformly slate-grey, with the exception of the brown club of the antenna
and a black median band on the elytra. This band is a little more than 1 mm.
wide at the side ; it narrows slightly above and does not quite reach the suture.
In the second specimen the band is broader and extends across the suture,
but is much shaded with slate-grey and only its anterior boundary is well defined,
while posteriorly the band fades away.
Possibly both this form and the preceding one may ultimately prove to be
colour varieties of M. oculatus. Several of the African Mecoceri closely resemble
certain Longicorns (e.g. Acmocera), and among mimetic species one must always
expect to meet with polymorphism.
4. Mecocerus modestus spec. nov.
cJ$. Signatura elytrorum M. annulipedi Karsch (1882) simillimus, sed
constructione M. clathrati Jord. (1903).
Long. (cap. excl.) 8-10 mm.
Hab. Johann-Albrechtshohe, C'ameroons (L. Conradt), 1 pair, type <$ ;
Cameroons, 1 <J and 3 ?$ ; Old Calabar, 1 <J.
Perhaps a colour-variety of M. clathratus, but agreeing on the upper surface
much better with M. anmilipes and even M. barombinus Kolbe (1895). The
head and rostrum bear the same deep and wide median groove as in M . clathratus,
the rostrum has the same length, being shorter than in M . annulipes, and the
velvety spot on the metasternum of the $ is as large as in M . clathratus. The
second tarsal segment and the apex of the first are black, not white as in M.
anmilipes.
The upperside is dull greyish drab with small greyish white spots : on the
pronotum a dot on the disc on each side of the middle and about three indistinct
ones on the sides, the grey pubescence being also slightly condensed in front of
the scutellum and at the lateral angles ; on the elytrum a spot behind scutellum,
another in first interstice further back, one in front of and three behind basal
callosity of which two in third interstice, one behind shoulder-angle, a slightly
transverse spot before middle at side-margin, three before apical declivity con-
262 NOVITATES ZOOLOGICAE XXVII. 1920.
fluent, forming a short transverse bar across interstices 3, 4, and 5, about six
small spots on apical declivity, a few minute dots or traces of them here and
there in basal three-fourths.
Underside rather more grey than upper, sterna with ill-defined lateral whitish
spots, and the upper posterior angles of the abdominal segments likewise whitish.
5. Physopterus cortex spec, now
$. Color Ph. melanoleuci Jord. (1913) ; magis robustus, capite cum rostro
latiore, antennarum scrobi multo majore, margine superiore ejus fere ad oculum
continuato ; capite inter oculos carina mediana instructo ; antennis prothoracis
basin fere attingentibus, articulis lc-4° longitudine aequalibus, 9° latitudine duplo
longiore, duobus sequentibus simul sumptis longitudine aequali, 10° multo latiore
quam longiore ; pronoto tuberculato, carina in medio interrupta atque antrorsum
flexa ; elytris leviter fasciculatis pone basin gibbosis ; prosterno laevi.
Long. 12 mm. ; lat. 55 mm.
Hab. Usambara ; 1 $.
A broad stripe, clay colour variegated with grey, extends from the apex
of the proboscis to the base of the pronotum ; apical area of elytra similarly
coloured ; scutellum and sutural area from base to the beginning of the apical
declivity greyish white, this area narrow at base, reaching sixth interspace behind
subbasal hump, narrowing abruptly before middle of elytra, and posteriorly
reaching into third interspace, the area appearing sinuate or constricted ; sides
of occiput, pronotum and elytra brown ; colour much less contrasting than in
Ph. melanoleucus . Underside grey, with inconspicuous brown lateral spots on
abdomen. Femora grey, brown at apex, tibiae grey and brown with three
indistinct brown spots, tarsi greyish brown. Head and rostrum much broader
than in Ph. melanoleucus ; a distinct median carina between the eyes. Rostrum
appearing less strongly widened at apex on account of the great width of the
basal three-fifths ; median channel deep and narrow at base ; dorso-lateral carina
very prominent, being a direct continuation of the rim of the eye, curved, the
two carinae not parallel, but first convergent and then slightly divergent ; upper
margin of antenna! groove curved and nearly extending to the eye.
Pronotum granulate, impressed before the scutellum and on the disc, with
a transverse row of four humps, of which the lateral ones are the most conspicuous,
being slightly penicillate ; depression in front of these humps without a raised
median line ; carina as in Ph. melanoleucus, curved forward in middle and
interrupted.
Prosternum with some granules anteriorly on the sides, otherwise smooth,
intercoxal process broad, also in mesosternum, where it is half as broad again
as long. First foretarsal segment as long as fourth.
The club of the antenna is slenderer than in the allied species, segment IX
being as long as X and XI together ; X is half as broad again as long.
6. Physopterus emmides spec. nov.
$. Niger, supra albo-griseo et russo variegatus, capite inter oculos griseo,
elytris ante et post medium densius grisescentibus, his areis ad suturam coniunc-
NOVITATES ZOOLOGICAE XXVII. 1920. 263
tis, antice ad scutellum continuatis ; subtus cum pedibus griseus, tibiarum
dimidio basali supra plus minusve rufobrunneo.
Rostrum supra planatum, biearinatum, sulco profundo mediano instructum,
lateribus impressum atque praeter earinam profunde sulcatum, sulco sub-oculari
etiam profundo. Antenna prothoracis basin paulo superans, articulo 3io secundo
longiore, clava tenui, 10° latitudine fere dimidio longiore. Pronotum convexum,
leviter quadri-impressum, carina dorsali fere recta medio levissime interrupta,
versus latera paululo convexa. Elytra basi marginata, ad suturam parum
deplanata, gibbositate postbasali distincta non-penicillata, interspatio 3'° pone
medium caeteris magis convexo, dilatato.
Long. 12 mm. ; lat. 5'5 mm.
Hab. Mundane, Cameroons (R. Rohde) ; 1 $.
The grey pubescence of the upperside is densest on the frons, in the middle
of the pronotum, and, on the elytra, in between and behind the subbasal humps
and behind the middle, but is nowhere so conspicuous as in Ph. melanoleucus,
and numerous small grey speckles are present on the russet portions of the
upperside.
The rostrum very strongly dilated at the apex ; the median sulcus deep,
continued on to the frons, but here shallow, not extending to the middle of the
rostrum, a narrower, more shallow and shorter sulcus beyond middle replaced
on widened apex by a raised line. The carinae broad, not sharp, particularly
broad at the eye, accompanied laterally for some distance by a deep groove which
is placed almost underneath the carina ; sides of rostrum concave ; cariniform
margin of antenna! groove curved, directed towards the underside of the head,
joining the anterior margin of the deep, curved, genal groove. Frons at its
narrowest point only as wide as the second antenna! segment is long ; occiput
russet, centrally variegated with grey. Lengths of antennal segments II and III
and VIII to XI are respectively 7, 10, 8, 10, 7, 9. Pronotum without conspicuous
granules and without humps ; on the disc four shallow impressions, of which the
two anterior ones are the deepest. Elytra without tufts ; the rows of punctures
impressed, the dorsal interspaces slightly convex, the third, which is broad, more
distinctly raised, especially behind the middle. Mesosternal process broad,
apically dilated. First foretarsal segment one-fourth longer than last (exclusive
of claws).
7. Xylinades fustis spec. nov.
$. X. lanugicorni colore et statura similis ; antennis decem-articulatis,
articulis 10° et 1 1° in unum confusis.
Hab. Benito, Spanish Guinea ; 1 $.
The black median patch of the elytrum is larger than in X. lanugicornis
Dalm. (1833), joining the two limbal spots. The tomentum at the apical sutural
angle is rather long, forming a small tuft. The outer and under sides of the mid-
and hindtibiae bear the same minute grey pubescence which is found on the
upperside of the femora and tarsi. The anal sternite is shorter than in the $
of X. lanugicornis and has more numerous large punctures. The pronotum is
not so distinctly depressed before and behind the centre. The chief distinction
is found in the antenna, of which the club is shorter and consists of two segments
only, segment X being so completely united with XI that no suture is visible.
264 Novitates Zoolooicae XXVII. 1920.
8. Cylindroides ventralis spec. nov.
$ 9. Niger, albo pubescens, lateribus pronoti late ochraceo-fulvis, elytris
macula diffusa basali communi ac fascia communi ante apicem declivem sita
brunneo-ochraceis, hac fascia antice diffusa lateribus antrorsum continuata
postice linea nigrescente in utroque elytro convexa terminata. Pronotum postice
in medio depressum. Pygidium leviter convexum, sulco mediano instructum.
Abdomen $ longitudinaliter depressum, parte depressa brunneo hirsuta, meta-
sterno macula mediana hirsuta eodem colore.
Hob. Warn, Niger, ii. 1896, iv. 1897 (Dr. F. Roth), 2 <J<J, type; Benito,
Spanish Guinea, 1 ? ; Gaboon, 1 $ (A. Mocquerys).
The brown colouring on the upper surface is variable in extent. The
pronotum may be described as being clay-brown with a white median stripe
which widens strongly in front. The transverse band placed before the apical
declivity of the elytra is more or less sharply defined posteriorly, but quite diffuse
anteriorly, being limbally either separated from or connected with the clayish
limbal area which extends from the shoulder backwards. The tibiae bear two
brown spots, one at the base, the other in the middle ; the foretarsus is brown.
The pronotum is much less depressed centrally than in the other known
species, and the middle line not at all raised in the depression. The underside
of the J is characteristic, the longitudinal central depression of the abdomen as
well as a rounded central space on the metasternum being clothed with stiff
dark brown hair ; the margin of the penultimate abdominal segment is not
elevate in the depression. The first tarsal segment is shorter than in C. albo-
plagiatus Fairm. (1885).
NovitaTes Zooloqicae XXVII. 1920. 265
NEW GEOMETRIDAE.
By LOUIS B. PROUT, F.E.S.
Subfam. HEMITHEINAE.
1. Dysphania translucida turbatrix subsp. nov.
c? ?, 82-88 mm. Thorax above with the yellow anterior patch very broadly
interrupted by a blue-black band, leaving posteriorly only a narrow, broken
edging of yellow scaling. Abdominal yellow belts narrow.
Forewing with the white markings restricted, the subbasal patch almost
obsolete (dusted over with dark scales), the central band narrowed, the extra-
cellular spots wanting, the submarginals more or less reduced and containing
little or no yellow scaling. Hindiving with cell-mark small, dark border broader
than in t. translucida, behind M' commonly reaching almost to the cell ; the
contained yellow spots variable, but on an average considerably smaller than
in t. translucida ; those on either side of R1 and that before R' commonly dusted
over or subobsolete.
Solomon Islands : Choiseul, north side, December 1903, a series, including
the type <$ ; Vella Lavella, March 1908. All in coll. Tring Museum, collected
by A. S. Meek.
2. Dysphania translucida floridensis subsp. nov.
Like extreme forms of the preceding, but with the whole of the hindwing
unclouded between Ms and SM2. On the forewing the central band is purer
white, rather broad in cell, very strongly constricted at M!.
Solomon Islands : Florida Island, January 1901 (A. S. Meek). Type in
coll. Tring Museum.
Pending exact anatomical investigation, I now treat translucida Montrz.
(1856), tentans Walk. (1864), and tyrianthina Butl. (1882) as forms of a single
species, leaving open the question whether they shall be merged with the yellow
Moluccan numana Cram. As a rule, the tyrianthina group (tyrianthina Butl.,
fulvilauta Warr., semifulva Warr., and the new forms) can be distinguished by
the restricted yellow in front of thorax — but this character is shared by schoutensis
Joicey and Talbot (1916), which geographically belongs to the tentans series,
and very occasionally even extreme forms of tentans ab. velata Bastelb. show
signs of transition towards the same peculiarity ; the translucida group (t. trans-
lucida only) by the clean white areas, the broad (commonly confluent) yellow
markings of the hindwing, and tendency to develop yellow scaling distally in
the submarginal spots of the forewing — but the subalbata form of " tentans "
tends to approach this in the $. The tyrianthina group is generally also note-
worthy for the loss of the dark patch in the middle of the hindwing between
M! and SM2, which seems pretty constant in the other forms ; but this patch
develops in the new form turbatrix, commonly appears (though reduced) in
semifulva Warr., and is well developed (though differently shaped — long and ,
narrow, not confluent with the abdominal patch) in the type specimen only of
fulvilauta Warr.
266 Novitates Zoolocicae XXVI J. 1920.
3. Metallochlora misera sp. nov.
(J?, 20-22 mm. Face grey -green. Palpus in <J less than 1£,* with third
joint minute, in $ 2J, with third joint almost equal to second ; above grey-green
with a few blackish scales, beneath whitish. Crown green, narrowly white
between antennae. Thorax and base of abdomen above grey-green, beneath
whitish ; crests moderate, red-brown mixed with black. Legs whitish ; hind-
tibia in (J with the pencil rather strong, all the spurs short except the inner
proximal.
Wings shaped as in typical Hemithea, in ? rather broader, yet not quite so
broad as in M. grisea Prout (Novitates Zoologicae, xxii. 318). Forewing
with SC1 free, R1 connate or stalked, M' connate or stalked ; grey-green ; costal
edge spotted, whitish ochreous and black ; lines white, irregular, in part ill
defined ; antemedian from one-third costa, somewhat oblique outward, then
sinuous ; postmedian from beyond two-thirds costa, incurved at radials, then
rather strongly outbent, angled inward on submedian fold (here slightly thickened)
and more weakly outward on SMS, reaching hindmargin at about four-fifths ;
terminal line scarcely darkened, interrupted by whitish dots at veins ; fringe
grey-green. Hindicing with antemedian line wanting, postmedian well
expressed ; very slight indications of dark cell-mark ; termen and fringe as on
forewing.
Underside whitish ; forewing with slight flush in middle and with costal
edge spotted.
Bingerville, Ivory Coast, August 16-18, 1915, type o, May and June 1-7,
1915, 2 $$ (G. Melon). In coll. Tring Museum. A <$ from Bopoto, Upper Congo,
May 1903 (Kenred Smith), too poor to describe, has long stood in the same
collection.
Near grisea Prout, but differently coloured, postmedian line more angulated
on fold, etc.
4. Chlorissa allochroma sp. nov.
9, 24 mm. Palpus 21, second joint with suberect scales above, third joint
strongly elongate ; red above, whitish beneath. Vertex and thorax concolorous
with wings ; abdomen very slightly crested anteriorly, posteriorly paler.
Fiirewing broader than in solidaria Guen., termen rather straight and not
very oblique anteriorly, much more oblique and slightly waved from M' ; SC
connate with SC!"S, not touching C, R1 from stalk of SC!"5, DC1 strongly oblique
posteriorly, M' shortly stalked; light cinnamon-rufous, irrorated and strigulated
with white as in solidaria ; costal margin more olive-brownish, darkening apically ;
lines thick, brown, slightly irrorated with black ; antemedian oblique outward
from before one-third costa, rather strongly sinuous, the inward curves being
at M and SM: ; postmedian from two-thirds costa to hindmargin rather near
tornus (median area consequently rather broad), angled outward on R\ incurved
between radials and more deeply between M' and SM2 ; antemedian proximally
(very narrowly) and postmedian distally edged with white ; terminal dark line
indicated in anterior part only ; termen minutely dotted with white at vein-ends ;
* In this article I have adopted Meyrick's convenient terminology, length of palpus being
given in terms of diameter of eye, that of antennal ciliation in terms of diameter of shaft, that of
tarsus in terms of length of tibia.
NOV1TATES ZOOLOQICAE XXVII. 1920. 267
fringe reddish, chequered with whitish opposite the veins, especially in posterior
part. Hindwing fairly broad, but with abdominal margin long ; termen
slightly waved, bent minutely at R1 and more markedly at R1 ; concolorous
with forewing ; antemedian line replaced by an elongate cell-mark ; the rest
as on forewing.
Underside dirty white, the forewing flushed with reddish and with some
smoky apical clouding ; markings obsolete ; terminal line of hindwing rather
strong from apex to R1, accompanied on wing-margin by very slight narrow
dark shading.
Bingerville, Ivory Coast, 1915 (G. Melou). Type in coll. Tring Museum.
May be provisionally placed in the vicinity of solidaria, in spite of its broader
wings, more sinuous postmedian line, and entirely different colour.
5. Prasinocyma eichhorni sp. nov.
2, 35 mm. Closely similar to perpolluta Prout (Novitates Zoologicae,
xx. 430), differing as follows :
Metathorax and abdomen entirely without the yellow dorsal line, the ab-
domen with some ill-defined purple-brown dorsal markings about the fourth
and fifth segments.
Forewing with termen slightly more curved ; costal margin purplish
chocolate, at base deepening towards Indian purple, only the extreme edge
narrowly white ; terminal line stronger ; fringe pale chocolate, not yellow.
Hindwing with the angle at R! rather pronounced ; termen and fringe as on
forewing.
Forewing beneath suffused anteriorly with purple-grey ; both wings with
fringe proximally nearly of the ground-colour, only slightly suffused, distally
nearly as above, though greyer.
Hydrographer Mountains, 2,500 feet, British New Guinea, April 1908
(Eichhorn brothers). 2 22 in coll. Tring Museum.
6. Comostolopsis stillata phylarcha subsp. nov.
2, 14-15 mm. Smaller than the corresponding sex of s. stillata Feld. from
S. Africa.
Forewing with all the red-brown spots well developed ; the red-brown
border, which in s. stillata consists of a mere thread, widened into a band
averaging "5 mm., broadest towards apex, its proximal edge crenulate.
Hindwing with corresponding distinctions, the cell-spot, in particular, enlarged.
Bingerville, Ivory Coast (G. Melou), type 2 and another ; Takwa, Gold
Coast (R. E. James). All in coll. Tring Museum.
7. Comostola ocellulata sp. nov.
cJ, 23-26 mm. In shape, ground-colour, and markings, similar to mundata
Warr. but larger, the ground-colour sometimes slightly more bluish, the hindwing
slightly less narrow.
Forewing with DC characteristic ; costal margin more or less strongly rosy
at extreme edge, then narrowly pale with dark irroration, on under-surface
rather broadly infuscated proximally ; cell-spot small, round, brighter red than
268 NOVITATES ZOOLOGICAE XXVII. 1920.
in mundata ; lines of white dots rather well developed, terminal red line very
slender, slightly interrupted. Hind/wing similar, except costally.
Arizan, Kagi district, Central Formosa, September 1906, July — August
1 908, a short series in coll. Tring Museum, the type August 1908 ; also in coll. British
Museum and coll. Joicey. Rantaizan, Formosa, May 1909 (a discoloured example,
aberrant in the larger — though equally round — cell-spots) in coll. Tring Museum.
This is no doubt the subtiliaria of Bastelberger {Iris, xxii. 173), but is very
distinct from iiympha Butl. and the accepted subtiliaria in the straight termen
of forewing, rosy costa, lack of red dots at outer edge of postmedian dots, etc.
Subfam. STERRHINAE.
8. Rhodostrophia calabra cypria subsp. nov.
cJ $. Foreicing with cell-dot well developed, though less large than in c.
tabidaria ; antemedian line generally thread-like or obsolescent ; postmedian
band narrowed, measuring only about 1 mm. ; submarginal shade nearly always
present, broad, but not very strong, separated from termen (as in c. tabidaria)
by a thread of the ground-colour. Hindicing with cell-dot obsolete ; postmedian
band more or less narrowed ; submarginal shade fairly well developed towards
tornus, weakening anteriorly. Underside in general more blurred than in the
other races.
Cyprus : Aghirda, May 7-14, 1916 (G. F. Wilson), including the type ;
Athanassa, on the plains, 465 feet, April 30 — May 6, 1916 (G. F. Wilson) ;
Troodos, June 24, 1916 (G. F. Wilson), July 14, 1911 (J. A. Bucknill) ; all in
coll. Tring Museum.
Like R. calabraria everywhere, this race is very variable in colour, etc., but
it seldom shows the bright coloration of the forms from S. and S.E. Europe,
and scarcely ever the division of the postmedian band into two lines, as in those
from Spain and France.
9. Rhodostrophia calabra transcaucasica subsp. nov.
$. In general almost as brightly coloured as c. calabraria from S. and S.E.
Europe, the outer pink shade, as in that, touching the termen, the postmedian
band nearly solid, not very broad, but rarely narrowed as in c. cypria ; both
wings with cell-dots sharply expressed, though not so large as in c. tabidaria.
Transcaucasia : Borjom. 6 $$ in coll. Tring Museum.
10. Organopoda olivescens orbiculata subsp. nov.
9, 34 mm. Larger than o. olivescens Warr. (Novitates Zoologicae, iii. 374)
from North Queensland.
Forewing with postmedian line more diffuse, rather more proximally
placed. Hindwing with the cell-dot slightly enlarged, containing a few
whitish scales, and enclosed in a round white spot which has a diameter of
nearly 1 mm.
Mount Goliath, Central Dutch New Guinea, 6,000-7,000 feet, February 1911
(A. S. Meek). 2 ?$ in coll. Tring Museum.
NOTITATES ZOOLOOICAE XXVII. 1920. 26 'J
11. Semaeopus orbifera sp. nov.
(J, 25 mm. Head, thorax, and base of abdomen above chocolate-brown,
abdomen becoming paler posteriorly, with narrow whitish posterior edges to
the segments ; underside mostly whitish, of palpus more ochreous, coxae and
forefemur tinged with ochreous and reddish. Antennal ciliation about 1.
Hindleg with tufts of hair partly dark smoky, partly dull ochreous, tarsus com-
pletely aborted, a large spreading pencil of ochreous to whitish hair.
Forewing not very broad ; SC2 from cell ; chocolate with some sparse whitish
irroration ; lines dirty white, irrorated — except in dots on the veins — with
olive-grey ; antemedian from one-fourth costa to one-third hindmargin, slightly
angulated outward on M and SM2 and marked by a pale spot on SC ; postmedian
from three-fourths costa to beyond two-thirds hindmargin, arising from a small
pale spot at costa, very slightly excurved anteriorly, finely lunulate-dentate
throughout, the teeth pointing inward on the veins ; cell-mark elongate, slightly
angled outward at origin of R-, white, edged with some grey scales, enclosed in
a large circular whitish patch of nearly 2 mm. diameter ; termen with slight
indications of a dark line, interrupted by white dots at the veins. Hindwing
not very broad ; termen rounded ; similar to forewing but without the first line.
Underside much paler, with the cell-mark and postmedian line indicated ;
cell-mark of hindwing with rather more extended dark bordering than above.
St. Jean de Maroni, French Guiana. Type in coll. Tring Museum.
12. Semaeopus simplicilinea Prout.
<3\ 25 mm. Closely similar to mitranaria Walk, and geminilinea Prout
(Novitates Zoologicae, xxiii. 382).
Forewing with ground-colour nearly as in geminilinea, but slightly brighter
ochreous, the dark irroration rather more reddish ; costal region and veins
not appreciably darkened ; median fine single, as in mitranaria : postmedian
approaching the subapical more closely than in geminilinea, and differing from
that of both the allies in being rather strongly incurved between the radials.
Hindwing coloured nearly as in geminilinea, but with the antemedian straight
as in mitranaria ; the ochreous, blackish-edged cell-mark considerably smaller
than in either of the allies.
Underside similar to that of mitranaria but slightly darker ; cell-mark of
hindwing reduced as above.
San Ernesto, Bolivia (68° W., 15° S.), 1,000 m., August— September 1900
(Simons). Type in coll. Tring Museum, determined by Warren as mitranaria.
A slightly larger, more reddish-ochreous example from Pozuzo, Huanuco, Peru,
800-1,000 m. (W. Hoffmanns) in the same collection.
13. Lipotaxia rubicunda (Warr.) ab. irregularis ab. nov.
(J, 20 mm. Ground-colour much lighter than in the name-type (Novitates
Zoologicae, xii. 324), only becoming more reddish on forewing towards apex,
at termen, and in the vicinity of a curved dark line which — as in segmentata Warr.
(Novitates Zoologicae, xiv. 220) — runs from base of M to about two-tbirds
hindmargin ; terminal patch small, dusky, ill-defined.
270 NOVITATES ZOOLOGICAE XXVII. 1920.
St. Jean de Maroni. 2 <$<$ in coll. Tring Museum.
Possibly a separate species though occurring together with typical rubicunda.
Of two worn specimens from San Esteban, Venezuela, in the Tring collection,
one appears to be referable to the name-type, the other to ab. irregularis.
14. Lipotaxia perpulverosa sp. nov.
<$, 21 mm. Closely akin to L. rubicunda Warr., perhaps a subspecies. Head
and body nearly as in the darkest examples of that species, abdomen above
noticeably infuscated.
Forewing with darker irroration than in rubicunda, the costal margin broadly
infuscated ; markings nearly as in rubicunda, the light apical and tornal patches
rather more strongly irrorated, connected by more definite mid-terminal shading
than in rubicunda ; a large greyish patch on hindmargin, shaped as in segmentata
Warr. but much less conspicuous. Hindwing appearing rather fuller than
in rubicunda, the abdominal margin being relatively less elongate ; much more
strongly irrorated than in rubicunda ; a minute ocellated cell-mark discernible ;
the interrupted subterminal line very fine, close to termen throughout, the apical
and the (obsolescent) tornal patch consequently minute — narrower and shorter
even than in segmentata.
Underside paler than in rubicunda, especially on the hindwing ; the dark
terminal shades weak, that of the hindwing narrow, rufescent rather than smoky
and only developed apically.
Rio Ucayali, Peruvian Amazons. Type in coll. Dognin. Also in coll.
British Museum from Chaquimayo, S.E. Peru, 2,500-3,000 feet, June — July
1910 (H. & C. Watkins).
15. Trygodes dissuasa sp. nov.
(J, 35 mm. Superficially scarcely distinguishable from small, well-irrorated,
weakly-marked forms of spoliataria Mosch. (Verh. Zool.-bot. Ges. Wien, xxxi.
407) = columbaris Butl. (Tr. Ent. Soc. Lond. 1881, p. 347) (Venezuela — Surinam
and Brazilian Amazons), of which it may well be a western representative, though
having clearly attained specific rank. Antenna, as in spoliataria* with short
lamellate teeth beneath and shortish fascicles of cilia. Midfemur glabrous,
wanting the long, dense hair-tuft of spoliataria.
Forewing with the green cell-marks reduced, consisting of a not very well
defined roundish one at DC1 and a smaller, very indistinct one at DC!.
Hindwing with the postmedian line almost obsolete, the green cell-mark fairly
distinct, circular, lacking the small anterior projection of spoliataria.
Quevedo, W. Ecuador (v. Buchwald). Type in coll. Tring Museum.
16. Ptochophyle nebulifera sp. nov.
<J$, 22 mm. Face cream-colour, upper edge vinaceous. Palpus vinaceous
on outer side. Vertex and antennal shaft cream-colour, slightly marked with
dull vinaceous. Thorax and abdomen cream-colour, tinged with Naples yellow.
Forewing broad, apex minutely produced, termen strongly curved from
SO, appearing gibbous in middle ; areole fairly long, SO shortly stalked beyond
* Mosehler calls them pectinate, which is inaccurate.
NOVITATES ZOOLOGICAE XXVII. 1920. 271
it ; pale Naples yellow to cream-colour, with irrorations and cloudings of olive-
grey to smoke-grey ; these occupy, in varying intensity, almost the whole of the
wings except a thick, interrupted submarginal line, which consists of more or
less confluent paired spots between SCS and R1, between R- and M1 (the anterior
of this pair slightly farther from termen), and narrower spots between M1 and
tornus ; the cloudings less dense towards base and in region of postmedian line
than elsewhere ; a minute black cell-dot ; fringe pale. Hindwing subquadrate,
but with the angle in middle rather more rounded off than in innotata Warr.
(Novitates Zoologicae, iii. 294), anal angle slightly produced ; M1 not or
barely stalked ; colours as on forewing, but with the ground-colour distinct
at base, in a conspicuous and rather broad postmedian band and a less conspicuous
antemedian ; subterminal row of spots more complete ; cell-dot white ; some-
times a darkened patch developed at abdominal margin between postmedian
and subterminal bands.
Underside much less clouded ; forewing with vinaceous costal shade, ex-
panding between SC and SC1 in their proximal part, and with vague vinaceous
shading in cell.
British New Guinea : Haidana, Collingwood Bay, April 1907 (A. S. Meek),
type <$ and a $ ; Hydrographer Mountains, 2,500 feet, April — May 1918 (Eichhorn
Brothers), 2 <J(J ; all in coll. Tring Museum.
17. Cosymbia maderensis azorensis subsp. nov.
tj$, 22-25 mm. Considerably smaller and (especially in the <^) decidedly
broader-winged than to. maderensis B.-Bak. (Tr. Ent. Soc. Lond. 1891, p. 216).
Reddish irroration generally denser, giving to the insect a much warmer tone.
Forewing with first line often well developed, strongly incurved anteriorly ;
median shade slightly less oblique than in to. maderensis, more reddish, commonly
very thick and strong ; postmedian row of dots often connected by a complete
line, both above and beneath ; cell-dot small, only very slenderly black-ringed ;
terminal dots rarely strong. Hindwing with corresponding distinctions.
Azores, a good series collected by Ogilvie Grant, recorded by Warren
(Novitates Zoologicae, xii. 441) as puppillaria Hb., and mentioned by me in
Seitz (Macrolep. iv. 150) under maderensis but not fully worked out ; type <$
" above Calheta S. Jorge, 200 feet, May 7, 1907." The true puppillaria only
occurred at San Pedro, Santa Maria, 2 $£, May 2, 1903, in a small, deeply-coloured
form which will probably deserve naming as a local race, in spite of the extreme
variability of puppillaria everywhere.
18. Anisodes (Pisoraca) iners sp. nov.
tj, 25 mm. Face whitish, upper edge buff. Vertex and antennal shaft
pale cream-buff. Palpus with third joint long ; whitish, above and on outer
side marked with dull red. Thorax, abdomen, and legs pale cream-buff, the
inner side of foreleg mostly dull dark reddish. Hindtibia rather rough-scaled,
the proximal spur well developed.
Forewing rather elongate, apex not acute, termen subcrenulate ; areole
long, SCS from before its extremity ; pale cream-buff, costally somewhat darker ;
slight scattered dark irroration ; a black dot on C near base ; an antemedian
series on SC, M, and SM! before one-third and a narrow dot on cell-fold rather
272 NOVITATES ZOOLOGICAE XXVII. 1020.
farther from the base ; a black cell-dot, followed by moderately thick buff median
shade, which curves inward very slightly behind middle ; a curved row of small
black postmedian vein-dots 2 or 3 mm. from termen ; small interneural brown
(buff parti}' overlaid with black) subterminal spots, namely a weak subcostal,
a stronger pair between the radials, one between the medians, and two almost
confluent cut by submedian fold ; conspicuous black interneural dots on termen
and minuter dots at vein-ends on base of fringe. Hindwing with termen sub-
crenulate, the teeth at R1 and R3 strengthened ; M1 separate ; similar to forewing,
without the subbasal and the first antemedian dot ; the black cell-mark larger,
somewhat elongate ; the median shade faint.
Underside with the ground-colour somewhat paler still, but with a great
part of the forewing (proximally and costally) flushed with pink ; both wings
with feeble cell-mark and postmedian and terminal dots ; forewing in addition
with a pinkish median shade and subterminal spots.
La Oroya, Rio Inambari, Peru, 3,100 feet, September 1904, dry season
(G. Ockenden). Type in coll. Tring Museum.
The smallest American Pisoraca known to me.
19. Anisodes (Pisoraca) obthesia sp. nov.
(J, 28-32 mm. Face brown above, whitish below. Vertex white. Occiput
brownish. Palpus slender, with third joint moderately long ; first and second
joints whitish beneath. Thorax and abdomen above pale grey, beneath whitish.
Legs more brown ; hindtibia with moderate proximal spur.
Forewing not broad, termen waved, tornus not strong ; whitish, irrorated
with light grey-brown, more densely at base of costa ; lines grey-brown, not
very strong, usually more or less thickened at costa ; antemedian from two-
sevenths costa, acutely bent outward in cell and again in submedian area ;
median and postmedian dentate outward on the veins ; median well beyond
cell-spot, slightly oblique inward to SC, then oblique outward to Rl, thence
about parallel with termen. a little incurved between Ms and SM2 ; postmedian
finer, nearly parallel with median, but curved instead of angled anteriorly ;
double subterminal shade strong, enclosing a row of irregular white subterminal
spots ; cell-spot small, black, somewhat elongate ; terminal line black, fine but
scarcely interrupted, thickened into dots between the veins ; fringe with minute
brown dots at vein-ends. Hindwing not broad, termen markedly crenulate,
the teeth at R- and (especially) R3 strong ; SC!-R' connate or short-stalked,
M1 well separate ; marked nearly as forewing, the cell-mark minutely pale-
centred.
Forewing beneath white distally and along hindmargin, with rosy suffusions
from base to postmedian line ; postmedian and proximal subterminal shade
well developed ; terminal line and dots brown. Hindwing beneath almost
unmarked.
Huancabamba, Cerro de Pasco, E. Peru (E. Bottger). 6 <JJ in coll. Tring
Museum.
20. Anisodes (Pisoraca) sypharioides sp. nov.
<J, 32-38 mm. Head and body concolorous with wings, only the extreme
anterior edge of vertex and inner edge of antennal shaft somewhat whitened.
NOTITATES ZOOLOGICAE XXVII. 1920. 273
Third joint of palpus elongate, but not quite as long as second ; upper and outer
sides marked with red.
Foreiving not very broad, apex rather acute, termen waved ; areole well
developed ; SC5 from or from just before its apex ; ochraceous-buff with very
fine rufous irroration ; antemedian and median lines rather thick, but faint, the
former from one-fourth costa oblique outward, sharply angidated in cell, then
waved, with a slight indentation on M and a deeper one on SMS, slight dots
developed on SC', M, and SM3 ; median denticulate, exteriorly somewhat ex-
curved, rather remote from cell-mark, posteriorly somewhat incurved, reaching
hindmargin scarcely beyond middle ; postmedian consisting of a row of distinct
blackish-red vein-dots, placed nearly as in sypharia Guen. (Oberthur, fig. 3360) ;
cell-dot small, white, very finely black-ringed ; termen with distinct interneural
dots ; fringe slightly paler, except against the terminal dots. Hindwing with
termen crenulate ; M1 widely separate from R3 ; concolorous with forewing,
in proximal part very slightly paler ; antemedian fine, curved ; median sinuous,
a little beyond cell-mark ; cell-mark large, black, with minute white pupil ;
the rest as on forewing.
Underside paler, posterior part of forewing and almost entire hindwing
inclining to whitish ochreous ; cell-marks and the markings beyond present,
the terminal dots prolonged into dashes.
Santo Domingo, Carabaya, S.E. Peru, 6,000 ft., January 1901, wet season
(G. R. Ockenden). Type in coll. Tring Museum. Also from Cushi, E. Peru
(W. Hoffmanns), coll. Tring Museum, and from Loja, Ecuador, coll. Dognin.
Has been misidentified with sypharia Guen., which has a different hindleg,
white vertex, unmarked underside, and other distinctions.
21. Anisodes (Pisoraca) endospila sp. nov.
<J, 36 mm. Closely similar to rufistigma Warr. (Novitates Zoologicae,
xi. 510), but larger and rather lighter, the ochreous cloudings on the pale ground-
colour being less strong. Face with a narrow but rather sharply defined dark
reddish band at upper edge. Metathorax with a pair of sharp black spots.
Foreiving with apex appearing slightly more acute than in rufistigma, the
termen being straight and strongly oblique ; costal margin slightly darkened
proximally ; lines finer, fairly well expressed ; cell-ring darker, rather more
elongate and (like DC3) oblique ; subterminal reddish spots before SC5, R! and
R1 strong. Hindwing with termen almost straight from the rounded apex
to the tail at R1, whereas in rufistigma there is an appreciable tooth at SC2 and a
pronounced one at R1 ; costal area pale, with the markings more or less obsolete ;
cell-ring as on forewing or slightly larger ; median shade thickening and blackening
at abdominal margin.
Forewing beneath with the rufous proximal clouding more transverse,
its strongest part suggesting an oblique diffuse antemedian line (in rufistigma
mainly longitudinal, occupying the greater part of the cell) ; median shade
obsolescent before SC5 ; subterminal spot in front of SC5 obsolescent ; cell-mark
blackish.
Carabaya, S.E. Peru (G. R. Ockenden) : Oconeque, 7,000 ft., dry season,
July 1904 (type) ; Agualani, 9,000 ft., wet season, October 1905 ; Santo Domingo,
6,500 ft., dry season, October 1902 (smaller — 33 mm.).
18
274 Novitates Zoologicae XXVII. 1920.
The type, otherwise in beautiful condition, has lost its abdomen, but the
other examples show this to be irregularly spotted dorsally with reddish, which
is not the case in rufistigma.
22. Anisodes (Pisoracai zeuctospila sp. nov.
<$ $, 27-29 mm. Face and palpus reddish above, whitish below. Palpus
with second joint in <J somewhat roughened above, not reaching beyond frons,
in $ rather longer and smoother ; third joint in $ moderate, in £ a little longer.
Head, thorax, and abdomen concolorous with wings. Hindtibia in $ rather
long, with coarse projecting sex-scales on inner side as far as the single proximal
spur.
Forewin abroad, apex blunt, termen curved, slightly waved ; buff (pale cream-
buff, with rather copious pinkish-buff irroration) ; costal edges irrorated with
blackish ; lines pinkish-buff ; antemedian rather thick but weak, excurved in
anterior half, a small indentation at submedian fold ; median shade rather
beyond middle, not very strong, somewhat dentate, somewhat incurved between
radials and more deeply between M1 and SM2 ; cell-mark rather weak, forming
a thick dash, midway between antemedian and median lines ; postmedian line
midway between median shade and termen, nearly parallel with former, finer,
more dentate, angulated inward near costa ; subterminal shades obsolescent,
but with characteristic inter-radial spots almost as black as in bipunctata Warr.
(Novitates Zoologicae, xi. 27), larger, confluent with a thick, equally black
streak along RJ to termen ; termen with small black interneural dots and more
minute, less black ones at the vein-ends ; fringe pale in distal half. Hindwing
broad, termen slightly crenulate, a rather stronger but still not prominent tooth
at R1 ; R'-M1 almost connate ; first line nearer base than on forewing ; median
shade almost obsolete (traceable at abdominal margin), the dentate postmedian
appearing as a continuation of median of forewing ; a small angulated white
cell-mark, with broad black circumscription ; subterminal shade obsolescent ;
termen and fringe as on forewing.
Forewing beneath with costal margin irrorated or suffused (in proximal
part broadly) with vinaceous ; some vinaceous suffusion in cell ; cell-mark and
the markings beyond reproduced in vinaceous ; posterior margin pale. Hindwing
pale, the postmedian line indicated, at least at costa ; distal area with some
vinaceous irroration ; terminal dots vinaceous.
Fonte Boa, Upper Amazons (S. M. Klages), August 1907 (type (J), May 1906
and July 1907 ($$), in coll. Tring Museum.
I have also before me a $ which may easily prove to represent an aberration
or local race of the same species from Suapure, Venezuela.
23. Anisodes (Pisoraca,i calama sp. nov.
<J, 25 mm. Palpus with third joint shortish-moderate. Hindtibia rather
thick, especially in proximal part, which is clothed with rather coarse reddish-
tinged sex-scales ; proximal spur long, distal pair shortish but unequal.
Close to stramineata Warr. (Novitates Zoologicae, vii. 145). Ground-colour
more yellowish, both wings with the reddish scales rather more sparse, but
mostly tipped with black, giving the insect a much more freckled appearance.
NOVTTATES ZOOLOGICAE XXVII. 1920 275
Markings the same, but rather sharper, median shade appearing more dentate,
postmedian with the teeth accentuated by black dots at the extremities ; sub-
terminal shades of forewing with more noticeable dark spots at radials and
medians. Forewing beneath much more sharply and brightly marked than
in stramineata.
Calama, Rio Madeira, below Rio Machado, August — October 1907 (W.
Hoffmanns). Type in coll. Tring Museum.
24. Anisodes (Pisoraca) difficilis sp. nov.
cJ$, 28-31 mm. Like the preceding species, but larger, slightly yellower
still. Hindfemur of $ with tuft of whitish and pale ochreous hairs in distal part,
opposed to a dense pale-ochreous sex-tuft on proximal part of tibia ; hindtibia
whitish, proximal spur long, distal pair shortish but unequal.
Upper Amazons : S. Antonio de Javary, May 1907 (S. M. Klages), type <$ ;
Fonte Boa and Rio Chucurras (Rio Palcazu), $$ ; in coll. Tring Museum.
Probably this or the preceding may be a subspecies of stramineata Warr.,
but as the $ of the latter is still unknown it is impossible to form a judgment.
I cannot at present distinguish the two new species by their markings, unless
perhaps the median shade of forewing in difficilis is more deeply bent at the
fold and the costal markings more darkened, i.e. with denser irroration.
25. Anisodes (Pisoraca) insitiva sp. nov.
<^$, 28 mm. Face above fawn-colour somewhat mixed with grey, beneath
whitish. Palpus with second joint reaching well beyond frons, third joint long
(little shorter than second) ; dull dark red, beneath whitish buff. Vertex and
antennal shaft a little paler than wings. Thorax and abdomen concolorous
with wings, the abdomen becoming a little paler at extremity. Foreleg mixed
with red on coxa, the tibia and tarsus infuscated above ; hindtibia with the
proximal spur long.
Forewing with termen slightly waved ; areole wanting ; dull fawn-colour,
with weak but rather copious darker irroration ; costal margin irrorated with
dark grey ; first line indicated by dark dots on costa (at 3 mm.) and on veins,
with a rather stronger, more distally placed dot on cell-fold (at 4 mm.) ; a
moderately large black dot on DO, with some dark scales behind it suggesting
the circumscription of an elongate ocelloid mark ; median shade very weak,
sinuous, in its anterior half midway between cell-dot and postmedian, then
curving proximad ; postmedian line chiefly indicated by dark vein-dots, strongest
in anterior half, those on SC2J (at their bifurcation) and R! largest and farther
from termen, the rest at about 15 mm. from termen ; termen with black inter-
neural dots ; base of fringe with minute dark dots. Hindwing with termen
appreciably subcrenulate, rather strongly convex in anterior part ; cell-spot
large, whitish, black-edged, strongly recalling that of obliviaria Walk. ( = sus-
picaria Snell., Tijd. Ent. xxiv. 80, t. 8, f. 6-6c, syn. nov.) ; median shade
almost entirely obsolete ; the rest as on forewing.
Underside paler, the forewing posteriorly and almost the whole hindwing
nearly white ; forewing with slight fuscous suffusion at base of costa and in
cell ; both wings with moderately thick dark cell-mark, extending nearly the
276 NOVITATES ZOOLOOICAE XXVII. 1920_
entire length of DC*"*, and with the postmedian and terminal dots present,
the latter elongate, especially on the hindwing, where they are connected by
an extremely fine line.
S. India : Palni Hills (W. H. Campbell), type $ in coll. L. B. Prout ; Nilgiris
(G. F. Hampson), in coll. British Museum (found among " -pallida Moore,"
which represented a heterogeneous mixture) and coll. Tring Museum.
Here also belongs the worn Anisodes recorded by me (Ent. Mitt. Deutsch.
Ent. Mus. iii. 244) as " Pisoraca sp." (p. 42) from Kosempo, Formosa; the
loss of one of the spurs of the hindtibia must have been due to accident or a
unique sport. The species is not like any other known in the subgenus Pisoraca,
its superficial resemblance being to small examples of obliviaria Walk., which
belongs to the subgenus Perixera ( = Phrissosceles).
26. Anisodes (Pisoraca) mesotoma sp. nov.
<J$, 28 mm. Face buff-pink above, whitish below. Palpus li, with third
joint in both sexes slightly deflexed, considerably shorter than second ; deep
red, beneath whitish buff. Head, thorax, and abdomen concolorous with
wings. Fore and middle legs in part reddened ; hindtibia in <J Ion" and slender,
the single proximal spur long and slender.
Forewing with areole well developed ; cream-buff with rather sparse but
coarse vinaceous (slightly rufescent) irroration ; cell-dot rather small ; lines
vinaceous ; antemedian zigzag, extremely ill-expressed, but marked with some
fine, black-mixed dots on the veins ; median better developed and more concise
than in most Pisoraca, only a little thickened and dentate-edged, gently curved
near costa and very slightly incurved in posterior part, placed little beyond the
cell-dot ; postmedian moderately distinct between the radials (where it shows
some tendency to form a pair of small confluent spots), and between M1 and
hindmargin (where it is somewhat sinuous and irregular, bent at fold), slightly
indicated in a subcostal spot, otherwise obsolete ; proximal subterminal shade
indicated by a few small spots, at least between R1 and R1 and before and behind
M! ; distal subterminal shade scarcely indicated ; intemeural dots at termen
and very minute vein-dots at base of fringe. Hindwing with termen faintly
waved ; similarly marked to forewing, but with the cell-spot forming a small
white, dark-edged ocellus, and the postmedian line rather finer and weaker but
less interrupted ; median line at least as firm as on forewing, rather straight
across middle of wing, a little curved anteriorly.
Forewing beneath paler, partly whitish, the costal region proximally with
pink suffusion ; markings (except first line) present, pinkish, the postmedian
line fine but fairly complete. Hindwing whitish, feebly marked.
Hainan : Henron, June 1904, type $ ; Youboi, June 1904, allotype $.
Lower Burma, a weakly marked $. All in coll. Tring Museum.
27. Anisodes tribeles sp. nov.
tJ $, 24-27 mm. Face red above, becoming pale to whitish below. Palpus
in <J over li, in $ about 2, in both sexes with third joint little shorter than second ;
red above, white or whitish beneath. Vertex and proximal part of antennal
shaft dirty white. Thorax and abdomen concolorous with wings. Foreleg and
middle femur in part reddened ; femora almost glabrous, hindtibia in J not
NOVITATES ZOOLOGICAE XXVII. 1920. 277
quite as long as femur, with three crowded spurs, all generally well developed,
the most proximally placed shorter than the other two (in Hainan and Formosan
specimens sometimes quite short).
Forewing rather short and broad, termen smooth, slightly curved, areole
well developed, SC! from its apex or little beyond ; cream-buff, coarsely irrorated
throughout with vinaceous rufous ; lines rufous, mixed with grey, antemedian
generally weak, placed well before one-third, somewhat curved, sometimes with
three small dark vein-dots ; cell-spot not minute, not darker than the lines ;
• median shade weak at costa, otherwise well expressed, anteriorly placed at
three-fifths wing-length or beyond, behind middle incurved : postmedian weak
or obsolete, but always marked with dark vein-dots, midway between median
shade and termen or slightly nearer the latter, slightly oblique outward from
costa, incurved between radials and very slightly behind M1 ; termen with weak
interneural dots ; fringe pale, least so proximally, with very minute rufous
dots touching the vein-ends. Hindwing rather broad, termen nearly smooth,
convex, especially between SC; and M1 ; first line usually indicated by minute
vein-dots ; cell-dot very small, white, narrowly dark-ringed ; median shade
close beyond it, straightish or gently curved ; the rest as on forewing.
Underside paler, especially the hindwing ; forewing somewhat flushed,
except at hindmargin ; median shade (at least on forewing) and postmedian
dots (on both wings) indicated.
Sudest Island, April 1898 (A. S. Meek), a short series, including the type,
in coll. Tring Museum. Also from Hainan and Formosa (Takow), doubtless also
in many other localities, though hitherto overlooked.
Exceedingly like some forms of compacta Warr. (Novitates Zoologicae,
v. 426), which is a true " Pisoraca," otherwise scarcely distinguishable ; third
joint of palpus a trifle longer, at least in <$, expanse generally less, upperside
rather duller, less weakly marked, underside paler, less glossy, the markings
better expressed ; apparently less variable, or at least I have seen no forma
with the black circumscription of the cell-dots materially enlarged or with any
additional cloudings, such as sometimes occur in compacta.
28. Anisodes viator sp. nov.
<J, 31-36 mm. Like prunelliaria H.-Sch. (Samml. Aussereur. Schmett. i.
t. 59, f. 329) in colour and markings, but considerably smaller, the wings relatively
shorter and broader. Hindleg of J; nearly smooth, except for a small femoro-
tibial hair-pencil (in prunelliaria the femur is hairy, the pencil perhaps stronger).
Abdomen less pale, with the dorsal dots at base weaker (less mixed with black).
Wings on an average rather deeper in colour, on account of the denser red
irroration. Forewing without definite red patches at base ; the red markings
more mixed with black ; median shade often nearer to the cell-spot. Hindwing
and underside with corresponding distinctions.
Carabaya, S.E. Peru : La Oroya, Rio Huacamayo, Tinguri, and Santo
Domingo (G. Ockenden), in coll. Tring Museum, the type from La Oroya,
September 1904, dry season. Also from San Antonio, W. Colombia, 5,800 ft.,
November-December 1907 (M. G. Palmer), in coll. L. B. Prout et coll. Dognin ;
and 1 £ from Chulumani, Bolivia, January 1901, wet season (Simons), in coll.
Tring Museum.
278 N0V1TATES ZOOLOGICAE XXVII. 1920.
29. Anisodes stigmatilinea sp. nov.
$$, 30-32 mm. Similar to urcearia Guen., but readily ^distinguished as
follows :
Hindleg of (J with strong hair-pencil arising from femoro-tibial joint and
extending fully one-half the length of tibia. First abdominal tergite with a
pair of black dots at its posterior end (the dot at anterior end of second tergite
also strong, the subsequent ones weakening). Wings relatively less broad ;
irroration stronger, dots on the antemedian and postmedian lines stronger, that
of the postmedian on R5 more displaced proximally ; median line rather sharper,
marked distally with rather noticeable dark dashes on R1, R1, and M1 ; cell-rings
rather more elongate.
Santo Domingo, Carabaya, S.E. Peru, 6,000-6,500 ft., November 1902,
wet season (Ockenden). Type <J and two ?$ in coll. Tring Museum.
30. Anisodes pilibrachia sp. nov.
cJ$, 22-27 mm. Almost exactly like ampligutta Warr. (Novitates Zoo-
logicae, iii. 376; Timor, Queensland, Louisiades, etc.), replacing it in New
Guinea, the Solomons, etc. Distinguished by the J foreleg which is quite
normal in ampligutta, but in the new species has the tibia and first joint of tarsus
densely clothed with felt-like hair. Third joint of palpus in £ slightly less
elongate. Ground-colour a little whiter, the thick shadowy lines consequently
standing out more sharply and giving to the insect a more variegated appearance ;
median shade in general even more acutely dentate ; cell-mark of the hindwing
subject to the same dimorphism — wholly black or only narrowly black-edged.
British New Guinea : Upper Aroa River and Milne Bay. Dampier Island.
Solomons : Bougainville (type in coll. Tring Museum), Choiseul, Vella Lavella,
Guizo, Kulambangra, Rendova, Isabel, Guadalcanar, S. Christoval.
It is interesting that the two allies occur together on Dampier Island.
31. Anisodes ( Stibarostoma) turned nom. nov.
Anisodes pallida Turn., Proc. Linn. Soc. N.S. Wales, xxxii. 691 (1908) (nee Moore).
I have already pointed out (Ent. Mitt. Deutsch. Ent. Mus. iii. 244) that
this interesting species has been misidentified. As it has never been named, I
have pleasure in dedicating it to Dr. Turner, whose able revision of the subfamily
has first made known its distinctive structure. The type will be from Queensland,
presumably in his collection. It also inhabits New Guinea, Rook Island, and
the Solomons.
32. Anisodes (Perixera) argentosa nom. nov.
Anisodes monetaria var. A. Guen., Spec. Gin. Lip. ix. 418 (1858) ; Oberth., Et. Lip. xii. fig. 3363
(1916) (Borneo).
This is clearly a valid species, not a form of monetaria. In monetaria, except
occasionally in the Ceylon form, the areole seems to be invariably wanting (India,
Malay Peninsula, Borneo) ; in every example of argentosa which I have seen
(Travancore, Khasis, Penang, Singapore, Borneo) a small areole is present.
Moreover, the distinctions, though slight, are sufficiently constant, notwith-
NOVITATES ZOOLOGICAE XXVII. 1920. 279
standing the variability of monetaria, and to the practised eye confusion is
impossible. The silvery spangle of the hindwing, so inconstant in monetaria,
is invariably large in argentosa. The following are undoubtedly mere aberrations
of monetaria : hyperythra Swinh., argentispila Warr., pleniluna Warr., areolaria
Guen. The race from the Moluccas, New Guinea and its satellite islands, the
Solomons and N. Queensland, is also variable, but I think tenable under the
name of Anisodes monetaria ceramis Meyr. (Tr. Ent. Soc. Lond. 1886, p. 209).
To which race (if either) homoslola Meyr. {Tr. Ent. Soc. Lond. 1897, p. 72 ; Talaut)
belongs it is impossible to judge on a single specimen, though its specific identifi-
cation is clear enough. Another single specimen, inornata Warr. (Novitates
Zoologicae, iv. 216 ; Banda Islands), seems to be a mere aberration of m.
ceramis, and is superficially a good deal like homostola.
33. Anisodes (Perixera) flavispila subsp. nov.
cj $. The white-grey ground-colour less tinged with brownish than in the
North Indian flavispila Warr. (Novitates Zoologicae, iii. 372) — which also
extends to Hainan — the discal ring of the hindwing only about one-half the
size, on underside generally wanting, never strong ; forewing beneath with the
cell-mark reduced in size.
Milne Bay, British New Guinea, November 1898 — February 1899 (A. S.
Meek), 4 $$, 2 $$ in coll. Tring Museum, including the type $. Also from
Humboldt Bay (Dutch New Guinea) and Fergusson Island, the latter mentioned
by Warren in describing the species.
34. Odontoptila elaeoides sp. nov.
<J $, 13-14 mm. Head black, the palpus beneath reddish ochreous. Antennal
ciliation of <J long. Thorax and abdomen olive, paler and more ochreous beneath.
Legs pale, the anterior pair more reddish, and on the upper and inner sides
spotted with black ; hindtarsus of <$ slender, about one-half the length of the
thickened tibia.
Forewing olive ; lines dark grey, the postmedian best developed, slender ;
antemedian excurved in cell, incurved behind ; median arising beyond three-
fifths costa, incurved behind middle ; postmedian parallel with termen except
posteriorly, where it bends almost to tornus, ending in a small dark tornal spot ;
terminal line fine, slightly interrupted at the veins ; fringe ochreous, dark-spotted
opposite the veins, especially near apex and at R1 and Ml. Hindwing with
termen toothed at R1 and feebly at R!, smooth posteriorly ; as forewing, but
with first line wanting and tornal spot rather ill-defined.
Underside reddish, the forewing smoky in cell and a part of disc, the hindwing
paler at abdominal margin ; median and postmedian dark lines well developed,
especially the latter ; forewing with tornal spot well developed.
St. Jean de Maroni, French Guiana. Type <$ and 2 $$ in coll. Tring Museum.
Much smaller and darker than subviridis Warr. (Novitates Zoologicae,
xi. 43) and mimica Dogn. (Ann. Soc. Ent. Belg. xlvi. 343), the two species to
which it comes nearest in shape, colour, and markings ; excisions in termen more
shallow, especially in the $ ; $ hindtarsus much shorter (in subviridis about as
long as tibia). Rather recalls " Ptychopoda " lignicolor Warr. (Novitates
280 Novitates Zoolooicae XXVII. 1920.
Zoologicae, xi. 41), which has still smoother margins, SC: of hindwing more
shortly stalked and the jj hindtarsus aborted, but which may possibly also have
to be referred to this genus, with whicli it agrees in the double areole, etc. ;
its $ is unknown and may prove to have a two-spurred hindtibia, while that of
Odontoptila has all the spurs well developed.
35. Scopula (Pylarge) plionocentra sp. nov.
cJ$, 18-22 mm. Face black. Palpus blackish, beneath pale. Antenna in
$ with the joints projecting, ciliate in long fascicles (about 2). Vertex, thorax,
and abdomen concolorous with wings, collar more ochreous. Foreleg mostly
blackened on upper and inner sides ; hindleg in $ rather long, the tibia slender,
with two long spurs, tarsus not abbreviated.
Forewing fairly broad, apex rather blunt, termen smooth, gently and regularly
curved, little oblique anteriorly, more so posteriorly ; pale ochreous whitish
with a tinge of flesh-colour ; a few scattered black scales in places ; cell-dot
small, sharply black ; lines greyer, rather diffuse and shadowy ; antemedian
from about one-third costa, excurved in cell, then very oblique inward to one-
fourth hindmargin ; median shade from costa well beyond middle (sometimes
at almost two-thirds), excurved well beyond cell-dot, slightly incurved at fold,
reaching hindmargin about middle ; postmedian line indicated by minute black
vein-dots placed on the proximal edge of the first subterminal shade, that on
R8 rather strongly displaced proximad ; pale subterminal shade sinuous, with
the inward curves at the radials and at the fold, placed between two feeble
greyish shades of about equal width and shape ; termen with minute black
interneural dots. Hindwing with costa rather straight nearly to apex, termen
gently rounded ; first line wanting ; median shade just proximal to the sharp
black cell-dot, slightly curving round it ; a postmedian shade-line in addition
to the two subterminal ones, separated from them by a narrow pale space ;
terminal dots as on forewing.
Underside rather glossy, forewing strongly suffused in proximal half ; both
wings with black cell-dot and pale subterminal with dark border on either side ;
terminal dots indicated.
Warri (Niger), 1897 (Dr. Roth), the type <J dated September, in coll. Tring
Museum ; also from Agberi (Niger), Abanga River (Gaboon), Masindi and Busiro
(Uganda).
Misidentified by Warren (Novitates Zoologicae, v. 242) as minorata
Bdv. (Faune Ent. Madag. 115) and made the type of a superfluous genus.
36. Scopula insincera sp. nov.
<J, 22 mm. Closely similar to sincera Warr. (Novitates Zoologicae,
viii. 208). Antennal shaft thicker, more strongly dentate, with longer fascicles
of cilia (about 2). Hindtibia not dilated, little longer than femur ; tarsus slender,
longer than tibia.
Forewing slightly less pure white (more creamy), subcostally with some
fine black irroration, which is wanting in sincera ; lines more direct, all nearly
parallel with termen, the first rather far from base, strongly oblique, the last
farther from termen than in sincera ; terminal dots virtually wanting.
N0V1TATES ZOOLOGICAE XXVII. 1920. 281
Hind/ioing with a few scattered black scales ; postmedian line more sinuous ;
last line placed farther from termen ; terminal dots obsolete.
Forewing beneath brown, only remaining whitish behind fold, in two narrow
outer bands (distally to postmedian and between subterminals) and on fringe.
Hindwing beneath with feeble postmedian line, two weak macular subterminals
and traces of terminal (strongest between the veins).
Johannesburg (E. A. Bacot), type in coll. L. B. Prout ; also a $ from Transkei
(Miss F. Barrett) in coll. British Museum ; the latter a sport with SC'-R1 of
hindwing stalked for about one-third of their length (normally in this species
and sincera about connate or barely stalked).
37. Scopula euphemia sp. nov.
(J$, 16-19 mm. Face and palpus black. Vertex whitish. Antennal joints
slightly projecting, ciliation little over 1. Collar tinged with ochreous. Thorax
and abdomen whitish. Hindtibia of £ little elongate, somewhat thickened
and flattened, fringed on upperside, tarsus little shorter than tibia.
Forewing rather narrow, costa very slightly curved, termen rather strongly
oblique, smooth, gently curved ; white, sprinkled with scattered black scales ;
lines light brown, rather thick ; antemedian very weak and diffuse, apparently
sharply angled outward near the cell-dot ; cell-dot strong, deep black ; median
shade strongly oblique from middle of hindmargin to SC5 near postmedian,
obsolete anteriorly ; postmedian line parallel with termen, 1*5 or 2 mm. therefrom,
lunulate-dentate, the teeth directed distad and blackened ; subterminal shades
feebly indicated ; a fine slight brown line on termen, marked with black inter-
neural dots ; fringe white, with some minute and sparse black irroration beyond
middle. Hindwing not broad, termen little convex, very slightly prominent
(through a change of direction) about R1 ; first line wanting, the other markings
continued, more proximally placed, the median shade preceding the cell-dot.
Underside similar, the forewing more suffused costally as far as the cell-dot ;
teeth of postmedian line less black than above.
S. Nigeria : Warri, August — October 1897 (Dr. Roth), type <J (worn) and
two $$ (good) ; Ilesha (Capt. Humfrey), a worn $. All in coll. Tring Museum.
38. Scopula erinaria isolata subsp. nov.
3, 25-26 mm. Forewing with the median line fine, passing midway between
the cell-dot and the postmedian (in e. erinaria Swinh., Tr. Ent. Soc. Lond. 1904,
p. 553, thicker, closely approximated or appressed to the postmedian) ; shade
beyond postmedian rather strong. Hindwing with median shade well proximal
to the cell-dot.
Transkei, Cape Colony (Miss F. Barrett). Type in coll. Tring Museum.
The hindtibia may be slightly thicker than in e. erinaria.
39. Scopula supina sp. nov.
<J $, 22-27 mm. Face red-brown, in part or almost wholly overlaid with
blackish. Palpus red-brown or blackish above, paler beneath. Vertex and
antennal shaft proximally slightly paler than the body, occiput narrowly black-*
edged behind ; antennal ciliation over 1 . Thorax and abdomen flesh-colour,
282 Novitates Zoologicae XXVII. 1920.
the abdomen with (generally indistinct) darker dorsal spots. Hindtibia in <J
moderately long, dilated, with strong hair-pencil, the tarsus about three-fourths.
Forewing rather broad, apex acute or even minutely produced, termen
smooth, straightish and little oblique anteriorly, somewhat more oblique
posteriorly ; flesh-colour, with slight and irregular dark irroration ; lines greyish-
fleshy, extremely oblique ; antemcdian indistinct, acutely angulated in cell
near the cell-dot ; cell-dot rather small, black ; median shade rarely thick,
slightly dentate outward on the veins, running from middle of hindmargin in
the direction of apex (or costa close thereto), but strongly angled at R' ; post-
median slender and weak, but accompanied by slightly elongate dark dots on
the veins, parallel with median, thus almost reaching the termen at R1, but
retracted anteriorly ; subterminal shades moderate or rather strong, the proximal
parallel with postmedian, the distal with termen, the pale space between in-
terrupted where they meet about the radials ; termen with interneural black
dots. Hindwing with costal margin fairly long, apical region well rounded,
termen smooth, little convex, the bend at RJ inappreciable ; markings of forewing
(except first line) continued, the median shade generally thick, proximal to
the cell-dot, anteriorly weak or obsolescent, postmedian line farther from
termen, pale subterminal line complete, though anteriorly narrow.
Underside paler and more weakly marked, especially the hindwing.
Unyoro and Uganda, a good series (chiefly o^) from various localities, mostly
collected by Dr. Ansorge, the type <$ from Kiorbezi, January 4, 1898. Also from
Songive River, Lake Nyassa. Also (mostly Jrf) in a generally smaller and more
deeply coloured form, which will perhaps require a subspecific name, from Ivory
Coast and Nigeria ; the $ seems, however, to be in general more deeply coloured
than the $ in this species.
This is the Emmiltis (?) minorata of Swinhoe (Tr. Ent. Soc. London, 1904,
p. 558), an equally unfortunate determination with that of Warren mentioned
under S. plionocenlra above. The present species is recognisable at a glance
by its shape and extraordinarily oblique postmedian line, which looks as though
it ran to the termen, the terminal dot between SC5 and R1 forming a direct
continuation of the postmedian dots.
40. Scopula penricei sp. nov.
cJ, 30 mm. ; $, 28 mm. Nearest sanguinisecta Warr. (Novitates Zoo-
logicae, iv. 53), differing as follows :
Face and palpus red-brown, merely irrorated with black, the palpus scarcely
pale beneath. Forewing with termen slightly more irregular, the bend (or change
of direction) about R'-M1 being more appreciable ; lines browner (less grey),
the first two weak, noticeably incurved in submedian area ; antemedian even
more acutely angulated subcostally ; postmedian making a rather wide sweep
anteriorly and with a minute tooth outward between SC' and SCS ; the markings
beyond blue-grey, consisting of an elongate curved mark between the radials
and a double spot between M! and SM! ; nearer the termen a pair of more or
less developed blackish dots at R1 and another pair at fold ; fringe more varie-
gated, dark-dotted opposite the veins. Hindwing with termen slightly more
waved, the angle at R' rather more pronounced ; median line more waved ;
NOVITATES ZOOLOGICAE XXVII. 1920. 283
postmedian rather straight, somewhat farther from termen, at least in middle
of wing ; fringe as on forewing.
Underside more fleshy ; forewing without grey cloudings, both wings, on
the other hand, with some conspicuous scattered black scales, especially on
anterior parts of forewing. '
Angola : Chella Mountains, April 1900 (Penrice), type <J and allotype §
in coll. Tring Museum.
Warren (Novitates Zoologicae, viii. 208) did not discriminate this from
true sanguinisecta. The leg-structure of the <$ seems to agree pretty closely —
hindtarsus about as long as the tibia, which is thickened, with hair-pencil, perhaps
less strongly than in sanguinisecta, but slightly damaged.
41. Scopula oliveta sp. nov.
cJ, 24 mm. Face black. Palpus small, black, pale beneath. Vertex white.
Antennal shaft proximally dotted with black ; ciliation 1. Collar ochreous
brown. Thorax and abdomen whitish. Fore and middle legs infuscated on
inner side.
Forewing rather broad, costa gently arched, apex fairly pronounced, termen
very faintly waved, more oblique behind R1 than anteriorly ; R2 from before
middle of DC ; white, in places with very faint olive-green tinge ; a black cell-dot ;
light olive-green postmedian markings, consisting of a small and weak dash in
front of SCS, an oblong patch 2 mm. in length behind SCS, crossing well beyond
R1 and proximally touching the succeeding patch at R2, and a somewhat pear-
shaped patch between R2 and hindmargin, its broad and rounded end anterior,
its greatest width (about R3-M') 25 mm., at hindmargin about -5 mm., here
proximally edged with some dark scales : indications of a narrow, paler olive-
green, subterminal shade, angled inward about R2, and becoming more distinct
near tornus ; a terminal row of interneural black crescents or flattened triangles ;
fringe shaded with olive-green. Hindwing with termen weakly bent at R1 ;
cell-dot larger than on forewing ; similar markings beyond, the postmedian
patches a little farther from termen, the subterminal shade slightly broader,
more distinct anteriorly than posteriorly.
Forewing beneath with the cell-dot obsolescent, the postmedian patches
shadowy, grey, the entire area proximal to this, excepting the hindmargin,
suffused with rosy grey, the subterminal shade obsolete ; fringe whiter. Hindwing
beneath unmarked, except for the cell-dot and terminal triangular dots.
San Jacinthe Valley, Theophilo Ottoni, Minas Geraes, spring 1908 (F. Birch).
Type in coll. Tring Museum.
A (J from Espirito Santo in coll. British Museum has the antennal ciliation
over 1, the hindtibia little thickened, but with the hair-pencils present, hindtarsus
about 1. I have seen a further example in the Oxford Museum.
42. Scopula polyterpes sp. nov.
cj, 20 mm. Face and outer side of palpus black. Vertex and antennal
shaft white ; ciliation about 1. Collar brown. Thorax and abdomen dirty '
white with some dark irroration, the abdomen with faint broad cloudy belts
284 Novitates Zoolooicae XXVII. 1920.
dorsally. Foreleg infuscated on upper and inner sides ; midtibia slightly infus-
cated ; hindtibia dilated, with strong hair-pencil, the tarsus almost 1.
Forewing with ternien smooth, gently curved ; dirty white with a tinge
of pinkish buff, the distal area predominantly ecru drab, the whole with sparse
dark irroration ; cell-dot black ; lines brown ; antemedian slight, commencing
in a fine, extremely oblique blackish line at one-fourth costa, forming a small
spot at SC 3 mm. from base, excurved in cell, then oblique inward, inbent behind
M and rather irregular ; median arising from a small dark spot beyond midcosta,
first running towards cell-dot, then oblique outward, acutely angled outward
at R1, then approximately parallel with ternien, but lunulate-dentate, sinuate
inward between radials and between M: and SM! ; postmedian fine, similarly
formed to median, accentuated by some small black dots on veins and a small
black mark on radial sinus ; subterminal line whitish, lunulate-dentate, pro-
jecting inward and thickened between radials and filled-in proximally with
slight paired dark spots in front of this and near tornus ; terminal dots sharp,
black, very slightly elongate, very slightly connected by a fine grey line ; fringe
brownish. Hindwing with ternien rounded, extremely weakly subcrenulate,
the projection at R1 scarcely noticeable ; proximally rather more coloured than
forewing, especially in vicinity of median line, where there is some cinnamon
suffusion ; cell-mark enlarged into an irregular ocellus of about -5 mm. diameter ;
first line wanting ; median line strong, incurved proximally to cell-mark, acutely
angled outward on base of M1 ; postmedian line and distal area nearly as in
forewing, the paired dark spots near tornus proximally to subterminal line more
strongly developed.
Both wings beneath (especially the forewing) more infuscated, and with
fine blackish cell-dot and dark median and postmedian lines ; subterminal line
and dark spots proximal thereto obsolescent on forewing, distinct on hindwing.
Porten, Hainan, July 1904. Type in coll. Tring Museum.
4"3. Scopula praesignipuncta sp. nov.
$, 20 mm. Similar to sybillaria Swinh. (Tr. Ent. Soc. Lond. 1902, p. 658),
but altogether more sharply marked.
Forewing with antemedian line well developed, rather regularly curved,
the proximal area with rather strong dark irroration ; cell-dot round, relatively
extremely large ; dark shading beyond postmedian rather strong, the pale
subterminal line thick, with a longer proximal projection between the radials
than in sybillaria and a rather ample one at tornus ; terminal dots strong.
Hindwing with the markings similar but not quite so strong, excepting the
cell-spot, which is fully as large as on forewing and slightly elongate along the
discocellulars.
Underside with pale band between cell-dot and postmedian line rather
noticeable.
Ryukyu Islands, June-August. Type in coll. Tring Museum.
44. Scopula ophthalniica sp. nov.
cJ$, 20-21 mm. Face black. Palpus black, narrowly pale beneath. Crown
white. Antennal shaft white, tinged with brown ; joints slightly projecting,
Novitates Zoolooicae XXVII. 1920. 285
ciliation in $ strong, rather over 1, in $ vestigial. Collar light brown. Thorax
and abdomen white, dorsally tinged with brown except at ends of abdominal
segments. Hindtibia in g thickened, a fringe of projecting scales on upperside
proximally, a thin hair-pencil on upperside from femoro-tibial joint, a stronger
pencil beneath ; hindtarsus in $ slender, over one-half. Wings slightly less
broad than in fibulata Guen.
Forewing white, with brownish cloudings and fine irroration ; lines brownish •
antemedian at one-fourth, oblique and slightly thickened from costa, angled
subcostally and again on M and SM!, between these two veins incurved and
slight ; cell-dot black, surrounded by a small, not very distinct, brownish ring ;
median line formed as in fibulata but rather less thick, placed rather more distally
to the cell-dot ; postmedian formed nearly as in fibulata, but with the tooth at
SC5 slighter, that at Rl rather longer and more acute ; distal area with shadings
nearly as in fibulata, the thick proximal projection of the white subterminal line
at the radials rather longer, that at the fold rather more angular and less compact ;
terminal dark line broken into interneural dots and not running round apex ;
fringe white, feebly dark-speckled. Hindwing much less dusted than in
fibulata ; markings similar ; proximal line more slender ; white subterminal
corresponding to that of forewing, the dark spots in its proximal side less confluent
than in fibulata.
Both wings beneath glossy, almost unmarked, the forewing strongly tinged
with brown-grey except at hindmargin, the hindwing white.
Bonthain, Celebes, 3,0C0— 7,000 ft., August 1896 (W. Doherty). 4 JJ,
1 $ in coll. Tring Museum.
Possibly a local race of ocellata Warr. (Novitates Zoologicae, vi. 33)
from Sambawa, but the $ antennal joints appear to project slightly less and
the hindtarsus may be a trifle longer.
45. Scopula pseudophema sp. nov.
<J$, 20-21 mm. Head and body concolorous with wings, the face mixed
with dark fuscous in upper part, the palpus mostly dark fuscous on outer side,
the abdomen with a row of blackish dorsal spots. Antennal ciliation in $ fine,
little longer than diameter of shaft. Hindtibia in <$ moderately dilated, fringed
above and with a strong hair-pencil from femoro-tibial joint, tarsus a little
over one-half.
Forewing rather broad, termen smooth, anteriorly straightish, then curving
and becoming more oblique ; whitish ochreous, in places tinged with rather
deeper ochreous ; black irroration minute and not copious ; lines fine and feeble,
formed of pink scales with a slight black admixture, almost or quite obsolete
at extreme costa ; antemedian from one-third costa, about vertical to middle
of cell, then oblique inward and sinuous to about one-fourth hindmargin ; cell-dot
small, black ; median line beyond, angulated outward on Rl, then oblique
inward and sinuous to middle of hindmargin, the deepest curve being inward
between M= and SM! ; postmedian about 2 mm. from termen, punctuated with
black dots or outward teeth on the veins, from M' to hindmargin (and sometimes
also more weakly anteriorly) overlaid with black scales, on R1 angulated outward,
incurved rather deeply between radials and very slightly between M1 and SM! ;
distal subterminal line somewhat similar to postmedian but weaker, only black-
286 Novitates Zoolooicae XXVII. 1920.
mixed in posterior half ; proximal subterminal represented by pink, strongly
black-irrorated spots except between the radials, the anterior two small and
round, sometimes weak, the two between R1 and M: elongate, those behind
M1 rather more proximal, subconfluent, smaller before than behind the fold, the
general arrangement strongly recalling the Palaearctic species Ptychopoda
dimidiata Hufn. ; termen with large black interneural dots ; fringe almost
unmarked. Hindwing with termen rounded ; markings similar to those
of forewing, antemedian line wanting, median proximal to the cell-dot.
Underside weakly marked, cell-dots, terminal dots, and on forewing also
the postmedian line and succeeding spots more or less well developed.
Tambura, Southern Bahr-el-Ghazal, type <J in coll. Tring Museum. Binger-
ville, Ivory Coast, July 28-31 (G. Melou), a $ in coll. Tring Museum. Sierra
Leone (A. Bacot), a more reddish ab. ($) in coll. L. B. Prout.
46. Scopula subpulchellata sp. nov.
(J$, 22-26 mm. Rather larger and paler than the Hainan forms of pul-
chellata Fab. ( = addictaria Walk.). Hindtibia in $ less strongly fringed above
than in pulchellata, the hair-pencil whitish (not ochreous, as in that species),
the tarsus a trifle longer.
Foreimng with antemedian line more uniformly expressed (in -pulchellata
commonly accentuated between M and SM, and often with minute blackish dot
near hindmargin, which is wanting in subpulchellata) ; discal ocellus larger but
rather vague, nearly always blind ; the characteristic markings distally to the
postmedian feebly developed. Hindtving scarcely distinguishable from that
of pale pulchellata, the postmedian line on an average less sinuate between the
radials.
Underside more weakly marked than in pulchellata.
Hainan : Manchyo, June 1902, type and others ; Secha, May 1902 ; Hoihow,
May 1902; Cheng-Mai, July 1902 and August 1904: Porten, July 1904;
Taipinshi. June 1906 ; a good series in coll. Tring Museum.
Mr. Burrows has kindly examined the genitalia of three males of subpulchellata
and two of pulchellata, and finds that they differ greatly. In the new species
the valves are fairly symmetrical, while in pulchellata the asymmetry is very
marked indeed ; in the former the socii are long, in the latter represented by
short horny processes ; the penis also differs widely. Indeed, subpulchellata
genitalia come much nearer in all respects to misera subtincta Warr. (Novitates
Zoologicae, iii. 372) from Tenimber, though the cerata are stouter and bowed,
and are more equal in length.
47. Scopula graphidata sp. nov.
(3\ 27 mm. Larger than perlineata Walk. {List Lep. Ins. xxiii. 775).
Ground-colour slightly whiter, but with a sparse, minute black irroration in
places which gives to it a slightly rougher aspect.
Forewing with antemedian line better developed, marked with dark dots
on the veins ; median line angled outward on SM8 ; postmedian fine, well expressed
throughout (brown, finely overlaid with blackish), with much deeper bays inward
at the folds, the proximal end of these more blackened than in perlineata ; proxi-
mal subterminal shade thickened in the bays of the postmedian ; terminal
NOTITATES ZOOLOOICAE XXVII. 1920. 287
dots strong, elongate. Hindwing with angle at R1 rather pronounced ; cell-dot
small ; postmedian line nearly as on forewing ; terminal marks strong, elongate,
almost confluent, the fine lunules of the posterior half giving to the wing-margin
a more crenulate aspect than in perlineata ; fringe more distinctly dotted at
vein-ends, the dot opposite RJ conspicuous.
Underside more strongly marked than in perlineata.
Celebes (W. Doherty). 2 £$ in coll. Tring Museum.
Presumably represents perlineata Walk, and spilodorsata Warr. (Novitates
Zoologicae, ii. 93) in Celebes, but provisionally I regard the three as distinct
species.
48. Scopula ochricrinita sp. nov.
cJ, 29-31 mm. Closely related to extimaria Walk. (List Lep. Ins. xxiii. 782).
Smaller. Hindtibial tuft ochreous and whitish-ochreous, without smoky ad-
mixture ; hindtarsus still shorter (one-fifth or less ; in extimaria about one-
fourth). Abdomen with the dorsal dots small.
Forewing with the black scales sparser than in extimaria ; no black subcostal
antemedian dot ; cell-spot forming a weak greyish oval mark instead of the
black dot of extimaria ; postmedian with the black marks usually smaller and
weaker ; terminal dots smaller, beneath weaker (but here showing more tendency
to be connected by a greyish line). Hindwing with all the black dots of
extimaria present, but reduced in size.
Khasia Hills, Assam, February 1894 (type), March 1894 (2 ££), October
1893 (1 (J, Cherrapunji), in coll. Tring Museum. Also a few other specimens in
different collections.
It should be added that stigmata Moore, sunk by Hampson to extimaria,
is a good species, or at the least a very distinct race, more nearly agreeing with
the new species in the cell-mark of the forewing above and in the continuous
terminal line beneath, but with blacker tibial tuft than in extimaria, tarsus still
less abbreviated, large blotches distally to postmedian of forewing, etc. Hamp-
son's description of extimaria (Faun. Ind. Moths, iii. 427) was evidently drawn
up mainly from stigmata.
49. Scopula anatreces sp. nov.
$, 35 mm. Face brown-black. Palpus blackish, narrowly pale beneath .
Vertex and antennal shaft whitish brown, about 12 of the proximal joints of
the antenna (after the first 2 or 3) each with a distinct black dot ; joints somewhat
projecting, bearing strong fascicles of cilia. Collar ochreous-brown. Thorax
and abdomen whitish brown, abdomen with a few black dorsal dots. Fore and
middle legs partly brown ; hindleg whitish, the tibia dilated and somewhat
elongate, with light ochreous-brown hair-pencil, the tarsus almost one-half.
Forewing very slightly narrower than in most of the moorei group, termen
oblique ; whitish brown, with sparse and minute black speckles ; cell-dot small,
grey, faintly and narrowly surrounded with brownish shading ; lines light brown ;
antemedian very fine and slight, but marked with black dots on the veins ;
median thicker, but weak, dentate, slightly more oblique than termen from
middle of hindmargin to R1 midway between cell-dot and termen, thence very
slightly oblique inward to costa ; postmedian fine, not strong, in part faintly
288 NOVITATES ZOOLOGICAE XXVII. 1920.
edged proximally with grey, between the radials with thick black conjoined
lunules, behind M: with three slighter ones ; this line is slightly oblique inward ;
from costa to cellule 7, acutely toothed outward on SCJ and especially on R1,
more minutely on R3 and M', these teeth punctuated with minute black dots ;
a ferruginous distal edging to the black radial lunules, succeeded by two short
thick ferruginous interneural streaks ; faint traces of similar pattern behind
M: ; subterminal shades very faint ; termen with strong black interneural dots ;
fringe with slight blackish dots at vein-ends. Hindwing with termen
faintly subcrenulate, with a slight but appreciable angle at R! ; antemedian
line wanting, median shade continued, straightish, just proximal to the cell-dot,
which is black and less small than on forewing ; postmedian line continued,
lunulate-dentate, more direct than on forewing, the blackening* and the ferru-
ginous markings beyond obsolete, except at extreme abdominal margin ; the
rest nearly as on forewing, the pale subterminal line apparently deeply incurved
between the radials.
Underside with cell-dots and terminal dots black, median shade and post-
median line well expressed, black-grey, the postmedian on both wings rather
strongly inbent between the radials ; forewing proximally suffused, its hind-
margin and the hindwing whiter.
Arizan, Formosa, September 1906, type in coll. Tring Museum. Other
examples from the same locality and of the same date in coll. Wileman (3 <$$)
et coll. British Museum (2 33).
Hitherto confused with S. moorei orientalis Prout (Ent. Mitt. Deutsch. Ent.
Mus. iii. 241). Hindtarsus rather longer, hindwing slightly more angled,
cell-spot of forewing concise, of hindwing black, postmedian line more deeply
inbent between the radials, terminal line less continuous, fringe-dots obsolescent,
median shade on forewing more dentate, on hindwing straighter, underside more
strongly marked. It is just possible that it may prove a remarkable dimorph
of punctatissitna Bastelb. (Ent. Rundsch. xxviii. 23 = quadrimacula Wilem.,
Ent. xlviii. 80, syn. nov.) ; <J antenna the same, tarsus apparently rather shorter,
wings rather narrower, paler, antemedian line more expressed, postmedian of
hindwing more distally placed, cell-spot of hindwing quite different.
50. Scopula ochrifrons sp. nov.
3, 30-32 mm. Face, vertex, and front of thorax clear light ochreous ;
collar deep ochreous ; palpus bright ochreous, mixed above with blackish.
Antennal shaft blackish, at extreme base ochreous ; ciliation long. Thorax,
abdomen, and legs white ; foreleg infuscated on upper and inner sides ; hind-
tibia greatly thickened, with strong hair-pencil ; tarsus abbreviated (about
one-fourth).
Forewing pure white ; costal edge very narrowly tinged with black ; veins
finely reddish grey, as in radiata Warr. (Novitates Zoologicae, iv. 434) ; first
line obsolete ; median line grey, more or less weak, rather thicker than post-
median, rather near the latter, especially at R1, where it is somewhat bent ;
postmedian fine, grey, 2 mm. from termen, almost parallel therewith, inappreciably
incurved behind M2, curved in front of R ' but almost obsolete anteriorly ; terminal
line faint ; fringe white. Hindwing weakly angled at RJ ; lines of forewing
continued.
NOVITATES ZOOLOQICAE XXVII. 1920. 289
Underside white ; forewing with costal margin infuscated, the dark shade
broad at base, narrowing distally, a scarcely appreciable rosy-grey flush in cell.
E. Peru : Pozuzo, type (in coll. Tring Museum) and others ; Huancabamba,
Cerro de Pasco ; La Merced, Chanchamayo. E. Bolivia : Charuplaya ; Chulu-
mani.
Intermediate between deiliniata Warr. (Novitates Zoologicae, iv. 433)
and radiata Warr., both of which, however, have the face black. Size of the
former, and with similar lines, though the postmedian is in general rather nearer
to the termen and the two subterminal shades (often developed in deiliniata)
are always wanting ; forewing much less flushed beneath, more blackened at
costa. Pure white colour and darkened veins as in radiata. S. leuculata Snell.
(Tijd-schr. v. Ent. xvii. 59, t. 4, f . 8 = ? nigricosta Dogn., Hit. Nouv. Amir. Sud.
iv. 8), which I have not seen, agrees in the ochreous head but has no markings.
51. Scopula contramutata sp. nov.
cj$, 21-24 mm. Smaller than immutata Linn. Antennal ciliation of <J
similar. Hindtarsus of <J relatively somewhat longer (about two-thirds) The
characteristic wing-form of immutata somewhat more accentuated (hindwing fully
rounded apically, straightish from before R1 to R!, slightly bent at R1:, again
straightish to near tornus). Both wings in $ on an average more ochreous than
in immutata, the lines fairly thick, the dentate form of the postmedian and its
inward curve between the radials always well noticeable ; forewing beneath
less uniformly infuscated than is usual in immutata, the markings consequently
standing out more distinctly. § very like a diminutive immutata 9, the post-
median line (as in $) characteristically dentate and incurved.
Chabarovsk, Ussuri Railway, June 4-22, July 14 and 30, August 9 and 19,
1910 (E. Borsow), 8 <J<J and 1 $ in coll. Tring Museum.
This is presumably the (hitherto unknown to me) Amurland " immutata "
of Staudinger and Rebel and may possibly be a subspecies, but I strongly incline
to regard it as distinct.
52. Scopula nitidissima sp. nov.
tj, 34-37 mm. Larger than pallida Warr. (Proc. Zool. Soc. Lond. 1888,
p. 322), purer white and even more glossy. Lines almost entirely obsolete,
the postmedian faintly discernible and sometimes the median and the proximal
subterminal ; cell-dots as in pallida, terminal dots entirely wanting, or at most
with a few very minute anterior ones discernible with the lens.
Kashmir Valley, 7,000 ft., July— August 1903 (Colonel Ward), type in
coll. Tring Museum. Also 4 $$ from Kulu, 1883 (Young).
I scarcely think this can be a form of pallida, as Colonel Ward took both
together without intermediates ; but in any case it is worthy of a separate
name. Unless the antennal ciliation be slightly longer and the hindtibial hair-
pencil slightly less strong, I can find no structural distinction ; hindtarsus aa
long as tibia.
53. Scopula okinawensis sp. nov.
cJ, 28 mm. Face black. Palpus mixed with black above and on outer
side. Vertex white. Collar ochreous. Thorax and abdomen white.
19
290 Novitatks Zoologicaz XXVII. 1920.
Forewing rather broad, termen smooth, slightly bowed ; white, with
extremely fine grey irroration ; costal edge tinged with buff, at least proximally ;
lines grey ; antemedian fine, obsolete anteriorly, straightish from SC nearly
5 mm. from base to hindmargin 3 mm. from base ; cell-dot minute, blackish ;
median shade weak, not very thick, obsolete anteriorly, straightish (the posterior
inward curve extremely slight) from SC at three-fifths wing-length to hindmargin
rather beyond middle ; postmedian better expressed, waved, in posterior half
parallel with termen (2 mm. therefrom), between the radials very weakly incurved,
anteriorly curving gently away from apex ; subterminal white line rather more
sinuous, hardly defined except by the absence of grey dusting ; termen with
blackish interneural dashes ; fringe white. Hind/wing with termen moderately
bent at R1, tornus pronounced ; first line wanting ; median shade very weak,
sinuous, proximal to the minute cell-dot ; postmedian slightly farther from
termen than on forewing, especially in middle, but bending slightly towards
tornus behind fold ; distal area as on forewing.
Forewing beneath with costal margin more broadly and brightly ochreous ;
otherwise somewhat suffused as far as the median shade, except at hindmargin ;
cell-dot indicated ; postmedian line well expressed, slightly thicker and browner
than above ; terminal dashes well developed, slightly connected by a fine and
weak line. Hindwing beneath white, with minute cell-dot and fine, not very
strong outer line, this occupying the position of the proximal subterminal shade
above, i.e. only about 1 '5 mm. from termen ; terminal line nearly as on forewing,
Okinawa, May 1904. Type in coll. Tring Museum.
54. Scopula flavifurfurata sp. nov.
^ $, 24-26 mm. Face black. Palpus black, pale beneath. Antennal
ciliation in $ apparently not long (damaged). Vertex, thorax, and abdomen
pale yellowish, body beneath paler ; collar ochreous. Fore and middle legs
somewhat infuscated on upper and inner sides ; hindtibia in q with moderately
strong hair-pencil, tarsus little abbreviated (almost three-fourths).
Forewing with apex minutely produced, termen more oblique in posterior
than in anterior half, very slightly waved ; cream-colour with a tinge of buff
and with minute dark irroration (mostly quite sparse, in costal region somewhat
more copious) ; cell-dot small, blackish ; lines buff, rather thick ; antemedian
rather before one-third, rather ill-defined, somewhat excurved in cell ; median
from costa somewhat beyond middle, curved and rather ill-defined anteriorly,
passing close beyond cell-dot and thence parallel with termen ; postmedian
midway between median and termen, little incurved at radials but with ill-defined
proximal teeth, slightly incurved at fold ; subterminal shades obsolescent ;
terminal dots minute and not intense ; fringe concolorous. — Hindwing with
termen bent at R5 ; cell-dot rather sharper than on forewing ; antemedian line
wanting ; median just proximal to cell-dot, little curved ; postmedian farther
from termen than on forewing, more incurved between radials ; proximal sub-
terminal shade better developed than on forewing ; terminal dots almost obsolete.
Forewing beneath somewhat suffused, especially costally ; minute cell-dot
present ; median and postmedian lines well developed, smoky, the postmedian
rather more proximal than above. Hindwing beneath paler, the cell-dot and
lines very feeble.
NOVITATES ZOOLOGICAE XXVII. 1920. 291
Subathu, July 1889 (type), August and June 1889 (2 $$), the last-named
an aberration of more pinkish-buff tone, more recalling furfurata Warr. (Novitates
Zoologicae, iv. 218), under which name Warren misidentified these examples.
55. Scopula proterocelis sp. nov.
cJ, 22 mm. Face and upperside of palpus blackish." Crown and antennal
shaft yellow ; antenna minutely ciliated. Collar ochreous-yellow. Thorax
and abdomen yellow, paler beneath.
Foreiving yellow, with very sparse minute dark specks (invisible to the naked
eye) ; cell-mark brown-grey, slightly elongate ; an irregular, not very strong,
brown-grey postmedian line, feeble at costa and between R3 and SM8, rather
deeply inbent and slightly thickened between the radials, incurved between
M1 and SM« ; rather distinct dark interneural dots at termen, connected by a
line of a slightly deeper yellow than the ground-colour ; fringe bright yellow.
Hindwing with termen slightly bent at R5 ; postmedian line obsolete ; cell-mark
accompanied distally by a red-grey spot resembling that of straminea Feld.
(Reise Novara, Lep. Het. t. 128, f. 33), but rather more anteriorly placed (between
SC2 and R3 — in straminea from R1 to the medians) ; terminal dots moderately
expressed anteriorly, becoming obsolescent posteriorly.
Underside paler, both wings with brown-grey cell-dash, sinuous postmedian
line (that of hindwing the weaker), and slight grey terminal line bearing indistinct
interneural dots.
Ilesha, N. Nigeria (Capt. Humfrey). Type in coll. Tring Museum.
At first sight remarkably similar to straminea Feld., which lacks the terminal
dots, has the postmedian line much less irregular above, obsolete beneath, etc.
56. Scopula rectisecta sp. nov.
cJ, 30 mm. Face and upperside of palpus black. Vertex and shaft of
antenna orange-ochreous ; antennal joints little projecting, ciliation rather
over 1. Thorax, abdomen, and legs pale yellowish ; forefemur darkened above ;
hindtibia rather long, strongly dilated, with hair-pencil, tarsus less than one-half.
Foreiving moderately broad, costa somewhat arched posteriorly, termen
smooth, very gently curved ; smooth yellow, without irroration ; costal edge
narrowly golden ; markings golden-yellow ; antemedian line obsolescent, dis-
cernible from M (just beyond origin of M2) to hindmargin ; cell-mark elongate,
not strong ; postmedian line straight, about 3 mm. from termen, not appreciably
nearer thereto at R1 than posteriorly, obsolescent costally ; no definite terminal
line, the ground-colour here slightly deepened ; fringe deep golden. Hindwing
almost inappreciably bent at R3; cell-mark indicated; postmedian line con-
tinued, complete, almost as straight as on forewing, reaching abdominal margin
2 mm. from tor.ius ; fringe deep golden.
Underside paler, unmarked ; costal edge and fringes nearly as above.
Bitje, Ja River, Cameroons (Bates). Type in coll. L. B. Prout, paratype
(rather smaller, worn) in coll. Joicey.
Intermediate in size and markings between transsecta Warr. (Novitates-
Zoologicae, v. 241) and laevipennis Warr. (Novitates Zoologicae, iv. 42),
postmedian line straighter than in the latter, less oblique than in the former.
292 Novitates Zoolooicae XXVII. 1920.
57. Scopula coangulata sp. nov.
(J, 24 mm. Face black. Palpus black, narrowly pale beneath. Vertex
and antenna cream-colour ; antennal joints slightly projecting, fascicles of
cilia rather long (about 2). Collar ochreous. Thorax and abdomen cream-
colour, above clouded with buff-yellow, the abdomen in addition with some
minute and sparse blackish irroration. Legs nearly as in the following species.
Forewing slightly narrower than in butyrosa Warr. (Proc. Zool. Soc. Lond.
1893, p. 362), termen scarcely waved, very gently curved ; cream-colour, some-
what clouded with buff or buff-yellow and with sparse black irroration ; lines
buff ; antemedian slightly oblique outward from one-third costa, bent in cell,
falling almost vertically on hindmargin at nearly two-fifths ; cell-dot black,
placed on a small roundish buff cloud ; median from well beyond middle of
costa, excurved (on R1 almost angled) far beyond cell-dot, then running inward
to fold at middle of wing, finally almost vertical to hindmargin but somewhat
dentate ; postmedian arising from a thickened spot on costa before three-fourths,
lunulate-dentate and highly irregular, forming an outward projection at SC5
and R1, deeply incurved between the radials and again rather deeply at fold,
the outward teeth accentuated by small black vein-dots ; subterminal shades
interrupted, especially the proximal, which is almost entirely wanting opposite
the inward curves of the postmedian ; terminal black dots small but distinct
in anterior half, very minute in posterior ; fringe concolorous. Hindwing
with termen very feebly bent at R3 ; first line wanting ; median curving proximally
round the cell-dot, somewhat angled outward at M ; cell-dot sharply black,
not surrounded with buff ; postmedian similar to that of forewing, but with
the irregularities less extreme and the dark vein-dots obsolescent ; proximal
subterminal complete, stronger than distal, and following the same course as
postmedian ; terminal black dots small, but the series complete.
Underside whitish, the forewing costally more shaded with buff and in
cell with vague reddish-smoky suffusion ; cell-dots present ; forewing also
with postmedian line (most distinct anteriorly), a slight thickening at its origin,
as above, and a suggestion of a similar mark indicating the origin of the median ;
terminal dots feeble.
$ similar but larger, the black central dot of forewing above weak or almost
wanting, leaving the roundish buff patch more noticeable than in the <$.
Khasia Hills, Assam (native collector). Type $ and 2 $$ in coll. Tring
Museum.
Warren labelled the <J inangulata, but it is very different from that species
except in the general course of the postmedian line.
58. Scopula sublutescens sp. nov.
(J, 20 mm. Face brown-black, narrowly pale below. Palpus brown-black
above, pale beneath. Vertex and antenna cream-colour ; ciliation fairly close
and even, scarcely over 1. Collar ochreous. Thorax and abdomen whitish
cream-colour, the thorax with some slightly darker admixture. Forefemur
and tibia infuscated on upper and inner sides ; middle leg more slightly infus-
cated ; hindtibia somewhat long, dilated, with long pale hair-pencil ; hindtarsus
about one-half.
Novitates Zoologicae XXVII. ]920. 293
Forewing with termen smooth, almost straight ; whitish cream- colour,
without black irroration (a few very minute fuscous dots in region of C discernible
with strong lens) ; lines rather thick and vague, darker cream-colour, inclining
to buff- yellow, wavy, all approximately parallel with termen ; antemedian from
beyond hindmargin, apparently angled in cell, but obsolete anteriorly ; median
from about middle of hindmargin, very slightly more oblique ; postmedian
rather finer than the others ; both subterminals developed, the pale line between
them rather thick, weakly sinuous ; no cell-dot ; terminal dots extremely minute,
scarcely traceable except in anterior part ; fringe cream-colour, unmarked.
Hindwing with termen very weakly bent at R3 ; markings of forewing continued,
except the antemedian.
Forewing beneath with vague reddish-smoky suffusions, except at hind-
margin and on subterminal line ; proximal part with some slightly darker
irroration ; a fine postmedian line and minute terminal dots faintly discernible.
Hindwing beneath whitish, unmarked.
Khasia Hills, Assam (native collector). 2 <$$ in coll. Tring Museum.
59. Scopula internata praeruptorum subsp. nov.
<J$, 25-30 mm. On an average considerably larger than i. internata Guen.
from South Africa. Ground-colour less ochreous, in the o generally fleshy-grey,
in the $ generally dark grey or ochreous-grey, in both sexes very variable.
Forewing with strong black dots on the fringe opposite the veins ; the
blotch at tornus rarely well developed, in this case oftener dark grey than reddish.
Hindwing with termen appearing slightly more irregular than in i. internata,
though this is in part an optical illusion due to the presence of a strong black
fringe-dot opposite the very slight angle at R3 ; fringe otherwise dotted as on
forewing.
Escarpment, British E. Africa, 6,500—9,000 ft., January to March 1901
(W. Doherty). A very long series in coll. Tring Museum.
GO. Scopula perfilata (Warr. MS.) sp. nov.
31?, 21-24 mm. Face black. Palpus blackish- fuscous above, light ochreous
beneath. Tongue strong. Vertex white. Antennal shaft whitish ochreous,
the minute serrations beyond the middle darker ; ciliation in $ nearly 2. Collar
ochreous. Thorax and abdomen whitish ochreous, the latter above with rather
strong blackish irroration, which usually condenses into more or less conspicuous
mediodorsal spots. Foreleg rather strongly, middle leg less strongly, infuscated
on inner side ; hindtibia of $ dilated, not markedly elongate, with a long pencil
of whitish-ochreous hairs, hindtarsus rather over two-thirds.
Forewing rather elongate, termen bowed, little oblique anteriorly ; whitish
ochreous, with moderate blackish irroration ; lines light brownish ; antemedian
weak, sometimes almost obsolete, strongly oblique outward from one-fourth
hindmargin, acutely angled in cell, scarcely traceable anteriorly, sometimes
marked with blackish dots on SMS, M, and SC ; cell-dots small but sharply
black ; median shade strongly oblique outward from middle of hindmargin,
vaguely defined distally, but generally appearing to throw out strong teeth on
the veins, strongly curved or angled in radial region, where it is far distal to the
294 Novitates Zoologicae XXVII. 1920,
cell-dot ; postmedian very near termen (2'5 mm. at costa, well within 2 mm.
in most of its course), chiefly expressed by blackish dots or minute dashes on
the veins, that on R1 displaced distally (1 mm. from termen), that on R*- more
proximal ; subterminal shades present but vague ; terminal interneural dots
(or short dashes) strong ; fringe somewhat irrorated, especially opposite the
veins. Hindwing with costa relatively rather long, termen rounded, tornus
prominent ; median shade thick, incurved round the cell-dot, sometimes also
with slight extension round cell-dot distally ; postmedian about 2 5 mm. from
termen, incurved between radials, accentuated by distal teeth on the veins ;
subterminal shades well developed ; termen and fringe as on forewing.
Underside without ochreous tinge ; forewing, except at hindmargin and
sometimes distal margin, with rather strong smoky suffusion, hindwing whitish ;
both with postmedian line and cell-dot well developed, terminal dots more or
less connected (at least on forewing) by a fine line ; fringes whitish, not or scarcely
irrorated.
Java : Bandong (type and others), Arjuno, Pengalengan (Preanger), a
series in coll. Tring Museum ; Sindanglaya, June 23, 1910, Nongkodjadja,
July 7, 1910 (E. A. Cockayne), 2 $$ in coll. L. B. Prout, kindly presented by the
captor, but hitherto awaiting determination.
Distinguishable at a glance from consimilata Warr. (Novitates Zoologicae,
iii. 313) by the narrower wings, which rather approach in shape those of the
African sublobata Warr. (Novitates Zoologicae, v. 19 = khakiata Warr.,
Novitates Zoologicae, xii. 389).
61. Scopula paradela sp. nov.
cJ$, 27-29 mm. Larger than delospila Warr. (Novitates Zoologicae,
xiv. 140). Antenna of $ with similarly projecting joints and long ciliation.
Hindtarsus considerably longer (over three-fourths ; in delospila about one-half
— Warren must have mismeasured). Abdomen without the minute blackish or
fuscous dorsal dots which are commonly developed in delospila. Ground-colour
slightly more creamy, without the slight violet-grey reflections of delospila.
Forewing slightly broader than in delospila ; black basal dot behind M
(omitted in Warren's description) wanting ; antemedian line complete though
not strong, not black-dotted on veins ; median shade less deeply incurved behind
middle ; postmedian rather near termen, less inbent at R! ; fringe in proximal
half more evenly irrorated, not developing definite dots at ends of veins.
Hindwing with cell-dot larger than in average delospila ; fringe as on forewing.
Biagi, Mambare River, British New Guinea, 5,000 ft., February — March 1906
(A. S. Meek). Type cj and 3 ?$ in C0U. Tring Museum.
62. Scopula homaema sp. nov.
(J$, 23-26 mm. Akin to the preceding, but scarcely a subspecies. Hind-
tarsus of (J scarcely three-fourths. Wings slightly broader still. Whiter, with
sparse irroration.
Forewing witli antemedian line rather more tremulous ; postmedian more
deeply lunulate-dentate, the projection at R1 appearing less acute (the anterior
part being less oblique inward), the inward curves between the radials and at
NOVITATES ZOOLOGICAE XXVII. 1920. 295
the fold, on the other hand, rather deeper ; terminal dots elongate ; fringe
proximally less irrorated, but with appreciable dark dots opposite the veins. ■
Hindwing with postmedian line correspondingly formed ; proximal subterminal
shade markedly crenulate ; fringe as on forewing.
Solomon Islands (A. S. Meek) : Isabel, June — July 1901, type $ ; Treasury
Island, Choiseul, Vella Lavella, Kulambangra, single??; all in coll. Tring Museum.
Also in coll. British Museum from Alu, Solomon Islands, misidentified as per-
UneatJ, Walk, by Butler (MS.), as undilinea Warr. by Hampson (MS.).
63. Scopula saphes sp. nov.
cj ?, 21-24 mm. Face black. Palpus black, pale beneath. Vertex white.
Antenna of $ subdentate, with fascicles of rather long cilia (about 2J). Collar
dull ochreous. Thorax and abdomen concolorous with wings. Legs mostly
pale ; foreleg partly infuscated ; hindtibia of £ dilated, somewhat elongate,
with long white hair-pencil and proximally fringed with white above, tarsus a
little over one-half.
Forewing rather broad, costa scarcely arched anteriorly, markedly so
posteriorly, termen smooth, very gently curved ; similar in colour to amala
Meyr., but slightly more olive-tinged, the blackish irroration less extremely
sparse, the markings olive-grey rather than ochreous ; cell-dot larger than in
amala, terminal dots strong though small ; first line strongly curved near costa,
median line thick, strongly excurved in anterior part, incurved behind cell ;
postmedian denticulate, slightly incurved between the radials and posteriorly ;
pale subterminal line rather thick, widening between the radials and near tornus,
the greyish shades which border it broad, fairly well developed, especially in
the $. Hindwing with termen rather strongly bent at R!, markings as on
forewing but first line wanting, median shade curving round proximal side of
cell-dot, sometimes partly surrounding it.
Forewing beneath pale greyish, hindwing whiter ; both with sharp cell-dot,
postmedian line and terminal dots ; median and subterminal markings also
traceable.
British New Guinea : Upper Aroa River, end of June 1903 (A. S. Meek),
3 (J<J (including type), 1 ? ; Hydrographer Mountains, 2,500 ft., January and
April 1918 (Eichhorn brothers), 1 $, 1 $.
64. Scopula heba sp. nov.
J?, 16-18' mm. Smaller than amala Meyr. (Tr. Ent. Soc. Lond. 1886,
p. 207).*
Forewing with the lines finer, especially the postmedian, which is also less
wavy ; median line rather more oblique than postmedian (in amala the two are
parallel). Hindwing with termen less noticeably bent at R1 than in amala ;
lines finer, postmedian less incurved between the radials.
Solomon Islands : Arawa, Bougainville (type) to Guadalcanal Also from
St. Aignan, Woodlark, and Rossel Islands. A fine series in coll. Tring Museum.
» Meyrick's measurements must have been made on the continental method— from tip to tip
in set specimens.
296 NOVITATES ZOOLOOICAE XXVII. 1920.
65. Seopula inactuosa sp. nov.
c?$, 15-19 mm. Similar to actuaria Walk. Hindleg in J with the knee-
pencil more conspicuous — apparently longer, oftener drawn out from the ab-
dominal cavity. Wings more glossy, on an average more weakly marked.
Forewing with apex a little more rounded, ternien rather less oblique ;
postmedian line thicker, less angulated subcostally, not punctuated with black
dots on the veins. Hind/wing with postmedian line similarly thickened.
Forewing beneath with dark glossy suffusion, which is rarely noticeable in
actuaria.
Lesser Sunda Islands, probably everywhere from Sambawa to Tenimber
(Sambawa, Sumba, Alor, Timor, Wetter, Dammer, Tenimber. in coll. Tring
Museum, the type from Tambora, Sambawa, 2,500-4,000 ft., April to May 1898,
(W. Doherty). Also from Key Islands, Toekan Besi, and, I think, Saleyer.
On the Sunda Islands name-typical actuaria does not occur, but is represented
by subsp. nigranalis Warr. (Novitates Zoologicae, iii. 378 = parumnotata
Warr., Novitates Zoologicae, v. 19, syn. nov.), which in weakly marked
examples almost loses the characteristic dark posterior spot of the postmedian
line, while in some examples of a. actuaria from Borneo this spot begins to manifest
itself, so that the races cannot be regarded as very sharply defined.
66. Seopula serena sp. nov.
cJ$, 16-18 mm. In structure, shape, and markings scarcely distinguishable
from lechrioloma Turn. (Proc. Linn. Soc. N.8. Wales, xxxii. 658), from Queensland.
The wings sometimes not quite as narrow, but rather variable.
Forewing slightly less white, more inclining to flesh-colour, sometimes even
assuming the pinkish-buff tinge of the minorata group ; irroration in general
rather less sparse than in lechrioloma ; antemedian line present, though weak ;
the other lines more retracted near costa, the median usually rather more oblique
than the rest ; terminal dots generally stronger than in lechrioloma. Hindwing
concolorous with forewing and with similar development of the terminal dots.
Forewing beneath (as also in lechrioloma) slightly infuscated, hindwing
beneath whitish, sometimes with the lines fairly well developed.
Freetown, Sierra Leone, 1914 (A. Bacot) ; type and others in coll. L. B. Prout.
Also from Ashanti, Niger, Angola, Unyoro, Kavirondo, British East Africa,
Nyassaland, Rhodes, Natal, Madagascar, Seychelles, in various collections.
Mr. Bacot bred the species ex ovo, the imagines emerging in February 1915.
The larva is extraordinarily long and thin, indeed thread-like, blackish brown
with some paler brown mottlings, and with the head, thorax, legs, anal end,
and prolegs almost entirely of the paler brown. That of lactaria Walk., which
was bred by Mr. Bacot at the same time, is much less extreme in shape and
is green in colour.
67. Seopula campbelii sp. nov.
<J $, 21-23 mm. Akin to aspilataria Moore, easily distinguishable as follows :
Hindtibia of q rather less thick, the tarsus rather longer (slightly over
one-half).
Forewing with ground-colour paler, in the J with very little, in the £ with
Novitates Zoological XXVII. 1920. 297
moderately copious (though very fine), dark irroration ; cell-dot distinct, though
very small ; median line rather more oblique than termen ; postmedian rather
more markedly crenulate ; proximal subterminal nearer to the postmedian than
on hindwing. Hindwing with median line more proximal ; a cell-dot as on
forewing ; postmedian less incurved between the radials (crenulate as on forewing).
Forewing beneath with strong smoky suffusion, leaving hindmargin and a
thick subterminal line and generally also a band between the median and post-
median lines whitish.
Palni Hills, S, India ( W. H. Campbell). A short series in coll. L. B. Prout,
including the type. Also in coll. British Museum.
68. Scopula pseudodoxa sp. nov.
rj$, 15-18 mm. Similar in structure, coloration, and markings to coundu-
laria Warr. (Novitates Zoologicae, v. 18), and the species which I identify
as thysanopus Turn. (Proc. Linn. Soc. N.S. Wales, xxxii. 663), all three being
perhaps races of a single widely-distributed species. Build rather more
robust than in coundv.laria, apex of forewing slightly less rounded, scaling less
glossy, ground-colour sometimes paler, markings less uniform, the median line
often weaker, the space between this and the postmedian often extended, post-
median in general somewhat more sinuous, proximal subterminal shade showing
more tendency to break up into spots. Forewing beneath more or less markedly
infuscated, which is not the case in coundularia.
Woodlark Island, March — April 1 897, type and others in coll. Tring Museum ;
St. Aignan ; Sudest, April 1898. All collected by A. S. Meek.
I strongly suspect this is the New Guinea " homodoxa " of Meyrick, but
as one of the most important structural characters he gives (Tr. Ent. Soc. Lond.
1886, p. 208) is " hindtarsus one-third" and this was evidently drawn from
the Tonga and Fiji relative, his name must be restricted to that species.
69. Scopula paradelpharia sp. nov.
tJ$, 15-18 mm. Face and upperside of palpus black. Vertex whitish buff.
Antenna with the proximal segments dotted with black above ; ciliation in <$
even, little over 1 . Thorax and abdomen pale pinkish buff above, whiter beneath.
Hindtibia in <£ rather elongate, dilated, with strong whitish hair-pencil ; tarsus
scarcely one-fifth.
Forewing of medium breadth, costa gently arched posteriorly, termen
smooth, very slightly curved, moderately oblique ; pinkish buff, sprinkled with
a very few minute black scales ; costal margin paler ; lines darker, less pinkish,
weak or obsolescent at costal margin, in part pale-edged (slightly reminiscent of
the New-World genus Scelolophia) ; antemedian fine, at about one-third, bent
in cell ; median generally firm, little thickened, bent near costa, slightly incurved
in submedian area, occasionally touching, but usually farther beyond, the minute
black cell-dot ; postmedian fine, excurved near costa, twice sinuate inward ;
subterminal whitish, sinuous, accompanied proximally and distally by moderate
shades ; terminal dots minute ; fringe almost unmarked. Hindwing with
termen smooth, rounded ; first line wanting ; median sometimes weak, generally^
proximal to, occasionally touching, the minute black cell-dot ; the rest as on
forewing.
298 N0V1TATE9 ZOOLOOICAE XXVII. 1920.
Underside whitish, rather glossy, the forewing tinged with cream -huff and
with the costal margin brighter ; unmarked, or (the forewing only) with the
faintest possible indication of greyish lines.
Bingerville, Ivory Coast, 1915 (G. Melon), a long series in coll. Tring Museum,
including the type. Sedhiou, Senegal, 1917 (H. Castell), a short series in the
same collection.
Probably widely distributed in Africa, representing the inficita group of
the Indo- Australian Region. A worn <J from Kilwa, German East Africa, shows
the same structure, and a $ from Mayotte, Comoro Islands, the same facies ;
other worn material is more doubtful.
The much shorter $ hindtarsus affords a ready distinction from adelpharia
Piing.
7". Scopula tumiditibia (Warr. MS.) sp. nov.
cJ$, 19 mm. Face black, pale at lower edge. Palpus mixed with black
above. Vertex whitish buff. Antenna! joints in J slightly projecting, ciliation
2. Thorax and abdomen concolorous with wings. Foreleg as far as first joint
of tarsus darkened on inner side ; hindtibia in <J enormously developed, about
as long as abdomen, strongly dilated and with a long ochreous-tinged hair-pencil
which reaches to the end of the extremely short tarsus.
Forewing rather narrow, termen smooth, very gently curved ; pale cream-
buff, clouded with pinkish buff and with some irregular black irroration ; lines
marked with stronger irroration ; antemedian weak, oblique from one-third
hindmargin, angled in cell ; median weak, excurved beyond the black cell-dot,
deeply incurved behind M1 ; postmedian irregular, lunulate-dentate, incurved
between the radials and behind M1, thickened at these points, especially about
R2 ; subterminal shades weak ; termen with sharp triangular black interneural
dots ; fringe almost unmarked. Hindwing relatively large, at least in the
<J ; termen smooth, rather full, especiall}' about Rs — M1 ; cell-dot in (J larger
than on forewing, paler in centre ; first line wanting ; median shade diffuse,
curving inside cell-dot ; the rest as on forewing.
Christmas Island (C. W. Andrews), in various collections ; the type (J
(March 1898) in coll. Tring Museum.
Misidentified by Hampson (Andrews's Monograph of Christmas Island, p. 71)
as optivata Walk. I see no special resemblance ; apart from the remarkable <J
hindtibia it differs in the narrower forewing, less fleshy colour, strong postmedian
markings at R!, large cell-spots of J (especially on hindwing), and other points.
71. Scopula latitans (Warr. MS.) nom. nov.
Accidalia reconditaria Snell., Tijdtchr. V. Enl. xv. 76. t. 6. f. 8, 9 (1872) (nee Walk. 1861), (Lower
Guinea).
Emmiltis latitans Warr. MS., in coll. Tring Museum.
Mr. Warren seems to have suppressed his latitans in favour of reconditaria
Snell., which he has clearly identified correctly ; but as the last-mentioned name
is preoccupied, I propose to substitute that of latitans.
NOVITATES ZOOLOQICAE XXVII. 1920. 299
ADDENDA.
During the months which have elapsed between my handing in the above
paper and its being found possible to send it to press, several further novelties
have been worked out, and in order to bring my work as nearly as possible
up-to-date the following descriptions are added.
StJBFAM. HEMITHEINAE.
1. Comibaena multigruma sp. nov.
?, 29 mm. Face green, finely edged with white. Palpus white, mottled
with seal-brown at the ends of the first and second joints and on the third.
Crown green, with narrow white anterior edge. Thorax above green, with a
cream-whitish anterior band ; beneath white. Abdomen above green in middle,
with large anterior and posterior seal-brown blotches ; beneath white. Legs
white, with some blackish and seal-brown spots and dots, particularly at the
knees and on the whole of the foretibial tuft.
Forewing broad, with termen strongly curved behind middle ; SC1 rather
long-stalked, SC2 arising beyond SC5, R1 free, closely approximated, for a very
short distance, to the subcostal stalk, then curving away ; bright green, as in
the allies ; costal margin broadly whitish ; markings seal-brown ; cell-dot
small ; a small blotch (rather more chocolate than the rest) near hindmargin
2 or 3 mm. from base, not reaching M (resolvable with lens into separate though
dense irroration) ; a large, irregular distal blotch from tornus to R1, nearly
3 mm. in width at hindmargin, its proximal edge deeply indented at MJ and
excavated between Ml and R', where its boundary-line describes a weakly M-
shaped figure, its distal edge quitting the termen in front of M2, indented between
M1 and Rs ; termen with seal-brown interneural dots ; fringe mostly dark,
varying in intensity. Hindwing with termen rather fully rounded ; a small
cell-dot ; a large apical blotch, proximally sinuate behind R1, its posterior
boundary reaching R1 proximally but receding somewhat distally, two small
orange spots enclosed close to termen before and behind SC2 ; a very small dark
tornal spot ; terminal dots strongly elongate into dashes in anterior half ; fringe
as on forewing.
Underside whitish green, rather brighter at base of forewing, the cell-dots
present ; shadowy reflections of the dark blotches of upperside ; fringe paler
than above.
Hydrographer Mountains, 2,500 ft., British New Guinea, February 1918
(Eichhorn brothers). Type in coll. Tring Museum.
2. Neromia (?) propinquilinea sp. nov.
9, 27-32 mm. Face red. Palpus fully one, third joint distinct, not minute ;
reddish, beneath pale. Tongue well developed. Crown green, narrowly white
in front. Antenna lamellate, with curved teeth nearly as long as diameter of
shaft. Thorax and abdomen above green, with a white (in places yellow-tinged)
ridge from metathorax to the whitish anal extremity ; beneath whitish. Foreleg
reddish.
Forewing with termen less straight than in most Neromia, being curved or
300
Kovitates Zoolooicae XXVII. 1920.
almost bent in middle, more oblique posteriorly than anteriorly ; DC1 rather
deeply angled inward ; M' just separate ; bright light-green with some scattered
metallic blue scales and with fine, moderately distinct, mostly elongate, transverse
whitish strigulation ; veins slightly yellower green ; costal edge whitish, separated
from the ground-colour by a line of yellow ; lines whitish ; antemedian fine,
subobsolete, from before one-fourth costa to before one-third hindmargin, very
slightly incurved behind M ; postmedian at scarcely three-fifths, thus more
proximally placed than usual, nearly straight or slightly wavy, with faint
suggestion of outward teeth at the veins, at least at R1 and M" ; fringe yellowish
white. Hindwing with termen rather full, slightly bent about R1 ; SC"
Very shortly stalked or just separate, M' just separate ; first line wanting ;
second little beyond middle of wing, straightish from costa about to R!, then
very slightly curved, then again straightish ; fringe yellowish white.
Underside much paler, whitish blue-green, unmarked ; costal margin of
forewing buff, of hindwing whitish ; terminal line and fringe of both wings
whitish.
Sedhiou, Senegal, July 5-12 (type), March 25-27, May 21, 1917 (H. Castell).
All in coll. Tring Museum.
On both wings a very faint and minute reddish cell-dot is discernible with
the lens, placed on DC1 well behind the origin of Rs and suggesting together
with the white dorsal ridge of abdomen a definite affinity with the rubripunctilla
group of Neromia. The $ antenna being formed nearly as that of the $ of
clavicornis Prout (Novitates Zoologicae, xxii. 319), that of the S will probably
prove well pectinate, and the new species will link up Neromia with Neurotoca
in exactly the same way in which some species of Omphax link that genus with
Heterorachis. The angulation of DC is rather suggestive of Neurotoca, but is
perhaps not more extreme than in certain examples of Neromia picticosta, cohaerens
or impostura.
3. Microloxia polemia sp. nov.
$, 21-22 mm. Face red. Palpus fully 2, second joint with less strongly
projecting scales above than in herbaria Hb., third joint about as long as second ;
reddish above. Tongue developed. Antenna with joints scarcely projecting,
ciliation minute. Vertex green, very narrowly white-edged in front. Thorax
and abdomen above green, becoming paler posteriorly ; beneath whitish. Foreleg
mostly reddish on inner side.
Forewing broad, costa very gently curved, termen oblique, straightish to
R', then very slightly curved (about as in Syndromodes cellulata Warr.) ; SC
anastomosing with C, R1 barely stalked, R2 rather extremely placed, M1 connate ;
green, nearly as in Chlorissa cloraria Hb. or slightly deeper ; costal edge ochreous ;
lines whitish, extremely fine and feeble, sometimes not traceable ; antemedian
apparently about parallel with termen, not discernible in front of cell ; postmedian
farther from termen than in herbaria advolala, slightly bent inward in front of
Rs and more markedly behind MJ ; fringe concolorous in proximal half, with a
very fine whitish line at base, whitish green in distal half, separated from ground-
colour by a fine white line. Hindwing with termen rounded ; SC2 stalked,
M' stalked ; concolorous with forewing, the lines obsolete.
Underside paler green, unicolorous.
Novitates Zoologicae XXVTI. 1920. 30L
Kut-al-Amara, August 7 (type and another) and August 9, 1918, in coll.
L. B. Prout, kindly presented by the captor, Mr. P. A. Buxton.
Rather broader winged than halimaria Chret., to which possibly it is more
nearly related than to herbaria.
Subfam. STERRHINAE.
4. Anisodes (Pisoraca) poeciloptera sp. nov.
(J$, 36-45 mm. Closely akin to lutearia Dewitz (Verh. Leop.-Car. Alcad.
xlii. 84, t. 3, f. 17); sometimes almost identical in coloration, much more variable,
oftener more rufescent, the dark cloudings commonly stronger and more extended.
Hindfemur of $ clothed with curled hair, as in lutearia. Wings on an average
slightly broader.
Forewing with costal margin almost as strongly darkened as in leonaria
Walk. (List Lep. Ins. xxii. 635), which is distinguishable, inter alia, by the
glabrous £ hindfemur ; black dots on antemedian shade generally poorly
developed ; median shade not projecting distally at R1, on the other hand almost
or quite meeting the postmedian shade at R', with the consequence that a regular
oval pale patch stands out prominently between the dark costal margin, R',
the median and postmedian shades, providing a ready means for picking out
poeciloptera from its allies by eye ; distal cloudings at the radials and between
M1 and hindmargin commonly strong, though never obliterating the subterminal
and usually leaving a pale terminal spot in front of SM2. Hindwing with the
median shade thick, almost or quite confluent with the postmedian about R1
and M1 ; distal cloudings stronger than in lutearia, especially between M1 and
abdominal margin.
Underside also variable, but in general less irregularly mottled and irrorated
than in lutearia, the generality of forms being rather uniform ochreous or orange-
ochreous as far as the postmedian, and with diffuse rather ill-defined redder
cloudings distally.
Ivory Coast : Bingerville (G. Melou), a long series, including the type ;
Nigeria : Lagos, Warri, Degama.
Described from extensive material in coll. Tring Museum, but no doubt
generally distributed in collections ; hitherto assumed to be aberrant forms of
lutearia.
5. Anisodes (Pisoraca) dewitzi sp. nov.
Ephyra lutearia $ Dewitz, Verh. Leop.-Car. Akad. xlii. 84. t. 3. f. 21 (1881) (nee <J).
(2$, 32-38 mm. Again close to lutearia and with similar <J hindfemur.
Ground-colour browner (less yellowish).
Forewing with costal margin on an average rather more heavily dusted
than in lutearia, yet not presenting the darkened appearance of poeciloptera ;
markings nearly as in lutearia, median shade generally more slender, its teeth
at R1 and M1 weaker, the pale band beyond consequently appearing less inter-
rupted ; postmedian line of dots rather more incurved between the radials and
especially posteriorly ; distal cloudings at the radials always weak, those,
posteriorly to M1 on the contrary often (as in Dewitz's figure) very strong,
sometimes nearly black. Hindwing with corresponding distinctions.
302 NOV1TATES ZOOLOGKAE XXVII 1920.
Underside much as in the generality of poeciloptera, on an average more
reddish, the reddish distal cloudings more strongly pale-mottled in their outer
part.
Ivory Coast : Bingerville (G. Melou), including the type ; Nigeria : Warri,
Degama ; Gaboon : Lambarene, on the Ogove River ; Upper Congo : Yakusu.
Described from a good series in col. Tring Museum. Differences in the
shape of uncus, of tegumen, of valve, and its armature confirm the validity of
the species in this group.
As ab. (?) transmuta ab. nov. I describe a colour-form in which both wings
have a paler ground-colour, generally with a fleshy tinge, and all the markings
are olive-green. Bingerville, both sexes, including the type ; Warri, 2 $$.
Genitalia not yet studied, but as some nearly typical examples show a tinge of
greenish in the markings, I do not think this can be more than an aberration.
6. Anisodes paratropa sp. nov.
$, 46 mm. Differs from the lutearia group in having the termen of both
wings deeply crenulate, with pointed teeth at the vein-ends, that at R2 (especially
on hindwing) considerably shortened. In the absence of the $ it is not even
certain that it belongs to the same structure group.
Wings broad. Forewing deep fleshy, with olive-grey irroration ; costal
margin more densely irrorated, markings about as in dcivitzi, olive-grey ; ante-
median not very deeply curved outward in cell, bearing black dots on SC and
SM2 but scarcely on M ; cell-mark narrower than in dewitzi ; median shade
rather more vertical anteriorly, the proximal curve behind M1 very abrupt ;
distal shades rather vague, the posterior not stronger than the radial. Hind-
wing similar ; the white, dark-edged cell-mark rather more elongate than in
the lutearia group.
Underside paler than in the lutearia group ; the forewing except behind
fold, the hindwing scarcely except in distal area, with pinkish irroration or
minute strigulation ; cell-mark indicated, especially on forewing ; median shade
indicated on forewing only ; both wings with pinkish postmedian line, accen-
tuated by darker dots on the veins.
Nguelo, Usambara (Dr. Kummer). Type in coll. Tring Museum.
7. Anisodes (Brachycola) jocosa clara subsp. nov.
cJ$. Differs from the other eastern forms (j. fimbripedata Warr., Novitates
Zoologicae, ix. 355, and ghjcydora Turn., Proc. Linn. Soc. N.8. Wales, xxxii.
084) in having the dark irroration finer and sparser, the dark shading which
accompanies the zigzag median line almost entirely obsolete, the two costal
spots of this line sharply black ; the subterminal dots behind SC, the two between
the radials and the one between the medians sharply expressed. In all these
respects nearer j. jocosa Warr., from Assam, from which — like all the eastern
races — it differs in its rather lighter ground-colour and in having the median
line of both wings more distally placed, the cell-dot of forewing smaller and the
cell-ring of hindwing larger, more narrowly margined with black.
New Guinea, Admiralty, Vulcan, Rook, Trobriand, and Fergusson Islands.
Type cj from Upper Aroa River, British New Guinea, March 1903 (A. S. Meek),
in coll. Tring Museum.
Novitates Zoolooicae XXVII. 1920. 303
8. Anisodes (Brachycola) cora sp. nov.
<J, 36 mm. Close to niveopuncta Warr. (Novitates Zoologicae, iv. 48).
Body and wings above paler, less fleshy-tinged. Forewing with markings
more strongly expressed ; cell-dot enlarged into a small elongate ring, having
a few pale scales in its centre ; median shade more deeply dentate, especially
on R1 and M1. Hindwing with the termen slightly more crenulate than in
niveopuncta ; markings corresponding to those of forewing, the cell-spot formed
as in many niveopuncta, the small white pupil being surrounded by a moderately
thick black ring.
Near Oetakwa River, Snow Mountains, Dutch New Guinea, up to 3,500 ft.,
October— December 1910 (A. S. Meek). Type in coll. Tring Museum.
9. Anisodes ockendeni sp. nov.
(J$, 29-30 mm. Smaller than pintada Dogn. {Ann. Soc. Ent. Belg. xxxvii.
159) ; palpus in both sexes a little longer, second joint perhaps less rough-scaled
above ; hindtibia of <$ with a rather strong hair-pencil, proximal spur wanting.
Forewing rather less elongate than in pintada, the red irroration denser, the
grey cloudings, on the other hand, weaker, though variable (in the Huancabamba
specimens nearly as in pintada) ; cell-ring on an average smaller, though variable,
sometimes (as also sometimes in pintada, teste Dognin) predominantly black
with only a small white pupil: ; postmedian line of dots more proximally curved
anteriorly. Hindwing with corresponding distinctions.
S.E. Peru : La Oroya (including the type $), Tinguri, and Santo Domingo,
a long series in coll. Tring Museum, collected by G. Ockenden. Also from E.
Peru : Huancabamba, near Cerro de Pasco ; Ecuador : Paramba ; Colombia :
Muzo and Popayan ; Bolivia : Chulumani.
I cannot find that this variable little species has ever been named. Apart
from its less red colour, it differs from rufulala Warr. (Novitates Zoologicae,
xi. 510) in having the markings less oblique. Evidently Mr. Warren never
differentiated it, as specimens in the Tring Museum are variously labelled pintada
Dogn., urcearia Guen. (!), stramineata Warr., ochricomata Warr., dispergaria
Moschl., tolinla Schaus.
10. Anisodes curtisi sp. nov.
<J, 37 mm. Similar to alienaria Walk. (List Lep. Ins. xxvi. 1580). Lower
part of face whiter. Midtibia glabrous. Hindfemur glabrous ; hindtibia with
the proximal spur wanting. Forewing rather less broad ; venation normal
(areole present, as in alienaria, but SCS not arising — as in alienaria — from near
R1 and diverging, but running almost parallel with R1 throughout) ; less clouded
with fleshy grey than in alienaria ; cell-ring smaller ; median shade less broad.
Hindwing with corresponding distinctions.
Underside less clouded with pink than in alienaria, the pink markings
consequently standing out more distinctly.
Penang, January 1897 (Curtis). Type in coll. Tring Museum.
May be placed next to effeminata Prout (Ent. Mitt. Deutsch. Ent. Mus.,
iii. 244), which is a broader-winged insect, with rather longer palpus, differently
coloured face, different cell-mark of hindwing, etc.
304 NOVTTATES ZOOLOOICAE XXVH. 1920.
11. Anisodes incumbens sp. nov. .
<J, 38 mm. Nearly related to recumbens Warr. (Novitates Zoologicae,
ix. 358), differing as follows :
Wings narrower (termen of hindwing straightish from R1 to tornus, except
for the small teeth), ground-colour much more ochreous, markings grey with a
slaty tinge. Forewing with costal margin grey ; median line even more
oblique, reaching costa close to postmedian ; the shade which parts from it
about the middle of the wing and runs to termen between the radials better
developed than in recumbens, not interrupted. Hindiving with the cell-ring
less black and less elongate than in normal recumbens.
Markira Harbour, S. Christoval, May 1-9, 1908 (A. S. Meek). Type in coll.
Tring Museum, unfortunately unique.
Possibly a remarkable subspecies or aberration of recumbens, but this seems
scarcely credible. In a good series of that species before me from Bougainville,
Choiseul, Vella Lavella, Guizo, Kulambangra, New Georgia, Rendova, Isabel
and Florida Islands, there is nothing at all approaching it in shape or colour.
12. Anisodes epicoccastria sp. nov.
<J, 34 mm. Face narrowly red above, then whitish with red irroration,
which becomes weak below. Palpus with second joint reaching beyond irons,
third joint long (about = second joint) ; red above, white beneath. Head and
body concolorous with wings. Hindleg long and slender, glabrous, tibia with
terminal spurs only.
Wings in shape, colour, and markings almost exactly like an overgrown
griseata Warr. (Novitates Zoologicae, iii. 380), with the markings rather
shadowy ; but that species belongs to the section Stibarostonui , with essentially
different palpus. Forewing with the oblique shade from hindmargin between
antemedian and median lines to termen between the radials rather broad but
ill-defined ; terminal dots (as also on hindwing) minute and inconspicuous, red
rather than black.
Underside pale, extremely weakly marked.
Upper Aroa River, British New Guinea, February 1903 (A. S. Meek). Type
in coll. Tring Museum.
13. Anisodes (Perixera) faustina sp. nov.
(J$, 30-35 mm. Extraordinarily like the largest, lightest (most sparsely
irrorated) examples of festiva Warr. (Novitates Zoologicae, xiii. 90*), which
has the hindfemur glabrous. The new species, however, has the typical structure
of the section Perixera (Meyr.), the distal half, or rather more, of the $ hindfemur
bearing a suberect tuft of red hair. Face while in lower half (in festiva red
throughout). Otherwise absolutely constant differences can scarcely yet be
indicated.
Forewing with cell slightly shorter (appreciably less than one-half ; in festiva
almost one-half) ; cell-dot generally (in festiva very rarely) shaded with red ;
* Described with query as a Perixera, erroneously transferred to Pisoraca, Novitates Zoolooi-
OAE, xiv. 144. It is really a " Perixera " (in sensuWarr., nee Meyr.), i.e. an Anisodes in sensu Turn.
Novitates Zoolooicae XXVII. 1020. 305
median shade rarely (in festiva generally) touching the cell-dot. Hindwing
with a larger, predominantly red, patch at end of cell (but that of festiva is at
times larger and redder than in> Warren's type).
Forewing beneath in general less heavily suffused with red than in festiva.
Dutch New Guinea : Upper Setekwa River, 2,000—3,000 ft., August 1910
(type and two other JcJ), September 1910 (1 <J) ; Mount Goliath, 500 ft., February
1911 (1 $). British New Guinea: Biagi, Mambare River, 5,000 ft., February
1906 (1 9). All in coll. Tring Museum, collected by A. S. Meek. In the two
last-named localities festiva occurred with it.
14. Anisodes (Perixera) palirrhoea sp. nov.
cJ $, 30-34 mm. Facies and coloration of multi punctata Warr. (Novitates
Zoolooicae, vi. 330) * but considerably larger, perhaps slightly longer-winged.
Palpus of <$ with third joint longer (about as long as second). Face below less
pure white. Femoral tuft of $ deeper red.
Forewing with the cell-mark narrow, generally obsolete posteriorly, only
its anterior black dot sharply expressed ; median grey line deeply zigzag, its
proximal (interneural) and distal (neural) darker dots sharply expressed, so
as almost to suggest the appearance of a double line ; blackish confluent or
subconfluent spots between the postmedian and subterminal often well developed
costally, between the radials, and from M1 to hindmargin, though subject to great
variation. Hindwing with cell-mark much narrower than in multipunctata,
its outline extremely fine or subobsolete, chiefly marked by a large black anterior
dot and a small, more red-mixed posterior one ; median shade formed as on
forewing but often weaker ; distal dark spots nearly correlated to those of
forewing, the posterior one in the most strongly-marked examples forming a
large and conspicuous tornal patch, traversed by the pale subterminal.
Solomon Islands, widely distributed (Choiseul, Vella Lavella, Guizo, Kulam-
bangra, New Georgia, Rendova), strangely misidentified by Mr. Warren as
■porphyropis Meyr., and hence not hitherto described. Type from Vella Lavella,
March 1908 (A. S. Meek), in coll. Tring Museum.
15. Anisodes rudis sp. nov.
cJ $, 42-46 mm. Face and palpus red above, white below ; palpus fully 2,
third joint in both sexes about as long as second. Crown white, almost entirely
covered with black scales except anteriorly. Antenna blackened above, clavola
white beneath ; pectinations in $ long. Body above mostly concolorous with
wings, the thorax crossed in front by a narrow leaden-grey band, the abdomen
becoming paler at extremity ; beneath whitish, the pectus mixed with dull pink.
Midtibia of $ densely clothed with very long white and pinkish hair.
Wings robust. Foreiving with areole wanting ; vinaceous cinnamon,
with very fine dark-grey irroration, giving a general effect of hazel ; costal
margin blackish ; lines black-grey, rather diffuse and not very sharply defined ;
antemedian from before one-fourth costa, rather oblique outward to fold, then
obsolete, reappearing more proximally as a short streak from hindmargin 4 mm.
* I think this is a synonym of thermosaria Walk. (Lint. Lep. Ins. xxvi. 1607), but as I have
no Borneo material before me I prefer to use Warren's name.
20
306 NOTITATES ZOOLOGICAE XXVII. 1920.
from base ; median shade rather beyond middle, slightly excurved in anterior
half and incurved in posterior ; postmedian from five-sevenths costa, slightly
angulated inward subcostally, then forming a long and gentle outward curve,
at fold gently incurved, reaching hindmargin rather near tornus, some blacker
vein-dots on its outer side increasing its otherwise feeble crenulation ; cell-mark
rather long-oval, pale-centred but inconspicuous ; very faint indications of the
proximal subterminal shade ; terminal interneural dots minute and not strong.
Hindwing with termen very slightly or scarcely bent at R1 ; antemedian
line faint ; cell-dot sharply white, inconspicuously dark-bordered ; median
shadowy, apparently encircling the cell-dot, at abdominal margin rather more
distinct ; postmedian angulated at R', the black dots (or small dashes) more
sharply expressed posteriorly than anteriorly ; the rest as on forewing, the fringe
slightly paler.
Underside deep fleshy pink, the markings scarcely indicated ; terminal
dots rather distinct, partially — especially on hindwing — connected by a dark
grey line.
Near Oetakwa River, Snow Mountains, Dutch New Guinea, up to 3,500 ft.,
October — December 1910 (A. S. Meek). Type <J and 2 $$ in coll. Tring Museum.
A very damaged $ from Sandakan, N. Borneo, appears to agree perfectly, in
which case the species — like several of its congeners — has a wide distribution.
Evidently closely akin to sciota Turn. (Proc. Linn. Soc, N.S. Wales, xxxii. 692)
from N. Queensland and subrubrata Warr. (Novitates Zoologicae, xii. 10)
from the Solomon Islands.
16. Anisodes dispilota sp. nov.
(J, 30 mm. Structure of decussata Scheller (Sepp's Surin. Vlind. iii. 287,
t. 132) = delineate. Warr. (Proc. U.S. Nat. Mus. xxx. 428), the hindtibia being
extremely short, smooth, the first tarsal joint greatly elongate. Smaller.
Forewing appearing relatively broader, the costal margin being slightly
more arched, the termen behind R3 rather less oblique ; rather paler, or of a less
warm tone ; proximal markings weak ; longitudinal lines obsolescent ; cell-ring
minute ; the line beyond slightly less oblique ; postmedian line almost as in
decussata ; a dark blotch running from postmedian to termen between the
radials. Hindwing with a dark line close to base ; antemedian and median
lines slightly less approximated than in decussata ; postmedian rather less strongly
bent before middle ; a dark blotch between M- and abdominal margin, reaching
from postmedian line almost to termen.
St. Jean de Maroni, French Guiana. Type in coll. Tring Museum. A $
from Demerara, British Guiana (J. Rodway), in coll. British Museum.
17. Bytharia lucida angusticincta subsp. nov.
3, 36-42 mm. ; $, 48 mm. Both wings with the distal border considerably
narrower than in I. lucida Warr. (Novitates Zoologicae, vi. 14), from the
Bismarck Archipelago, only measuring 1*5 to 2 mm., at the apex of forewing
3-4 mm. ; its proximal edge scarcely crenulate.
Rendova, Solomon Islands, February 1904 (A. S. Meek). 4 <$<$, 1 ? in coll.
Tring Museum. A single <$ from Choiseul, slightly intermediate, but should
be referred here.
NOVITATES ZOOLOGICAE XXVII. 1920. 307
Remarkably similar to uniformis Swinhoe (Java, Sumatra, Borneo), which
is larger, the borders of a more leaden hue, separated from the ground-colour
by a whitish line.
18. Scelolophia littoralis sp. nov.
9, 19 mm. Similar to nycteis Druce (Biol. Centr.-Amer., Lep. Het. ii. 122,
t. 52, f. 28), to which I refer as subspecies the smaller, brighter ignifera Warr.
(Proc- U.S. Nat. Mus. xxx. 436) from French Guiana, and the large, heavily
clouded latifasciata Bastelb. (Enl. Zeit. xxii. 159) from W. Colombia. Hindtibia
without the rudimentary fourth spur, which is usually present in nycteis. Body
and wings dark, the forewing as far as the end of the cell (except costally) and
the hindwing in proximal half heavily suffused, thus most recalling nycteis
latifasciata.
Forewing with cell somewhat shorter, the median shade (which is curved
somewhat inwards behind the vague cell-mark) more proximally placed ; the
narrow dark sinuous postmedian band (characteristic of nycteis and the new
species) more proximally placed, scarcely farther from cell than from termen.
Hindwing with a vague sinuous median band parallel with the postmedian.
Barranco, near Lima, April 1, 1913 (H. O. Forbes). Type in coll. Tring
Museum, together with a more rufescent, almost uniformly suffused $ taken
the following day.
A J1 from Callao, in coll. British Museum, doubtless referable here, shows
nearly the same structure as nycteis, but has the sex-tuft of the underside of the
hindwing apparently rather less elongate and more concentrated (roundish) ;
wings rather broad, hindwing with termen slightly bent in middle, its underside
whiter. Recalls also damaria Schaus (TV. Amer. Ent. Soc. xxvii. 193), which
has no tuft on hindwing.
19. Scopula alma sp. nov.
<J, 19-21 mm. Face black. Palpus black, pale beneath. Vertex and
antennal shaft white, ciliation slightly over 1. Collar ochreous. Thorax and
abdomen concolorous with wings. Legs tinged with ochreous, the forecoxa
above and forefemur and tibia on inner side blackish ; hindtibia white, not very
long, dilated, with long hair-pencil, tarsus almost 1.
Forewing not very broad, termen very gently curved, moderately strongly
oblique ; white with a strong fleshy or fleshy-ochreous tinge (as in envutaria Hb.
or flaccidaria Zell.), and with scattered dark irroration ; lines more brownish
than in the species named ; antemedian obsolete costally, weak throughout,
excurved, rather near the cell-dot ; cell-dot small, black ; median shade oblique,
obsolete costally, moderately strong from R1 or R! near the postmedian to hind-
margin at or slightly before the middle, almost straight ; postmedian fine, not
very strong, slightly accentuated at the veins, placed about 1-5 mm. from termen,
parallel therewith, obsolescent costally ; subterminal line white, little undulate,
rather broader than in emutaria ; termen with sharp black interneural dots ;
fringe slightly paler, at the tips free from irroration. Hindwing with termen
very feebly bent at R1 ; antemedian line wanting ; median straight, well proximal
to cell-dot ; postmedian straightish or little curved, farther from termen than
on forewing ; subterminal nearly parallel with termen ; termen and fringe as
on forewing.
308 NOVITATES ZOOLOQICAE XXVII. 1920.
Forewing beneath slightly greyer, especially at base, hindwing beneath
somewhat whiter ; both with cell-dot and the markings beyond ; fringe whitish,
scarcely irrorated.
Nairobi, British East Africa. The type June 1905, paratype May 1906,
both in coll. Tring Museum, collected by F. J. Jackson.
Except in size, this rather recalls some of the tailed species — emutaria Hb.,
perlata Walk., etc. Perhaps near obliquisignata Bastelb. (Deutsch. Ent. Zeit.
1909, p. 319), which I have not seen.
20. Scopula opperta sp. nov.
<J$, 24-28 mm. Face black-brown, narrowly whitish below. Palpus
black-brown, whitish beneath. Antennal joints in £ slightly projecting, ciliation
about 1 . Vertex white. Collar more or less buff. Thorax and abdomen whitish,
dorsally with some grey irroration. Fore and middle legs somewhat buff, the
former somewhat infuscated on inner side ; hindleg white, tibia in <J dilated
with hair-pencil, tarsus almost 1.
Forewing shaped about as in nesciaria Walk. (List Lep. Ins. xxii. 750) ;
white, finely irrorated with olive-grey, which easily discolours to a more brownish
or fleshy tone ; costal edge narrowly tinged with buff ; lines olive-grey ; ante-
median fine and weak or subobsolete, generally traceable from cell at one-third
of wing-length to one-third hindmargin, with slight bend inward at fold and
sometimes a slight tendency to form small spots or dots in cell, at fold, and
behind M! ; cell-dot black, minute ; median shade obsolete costally, oblique
from Rl at two-thirds wing-length to scarcely beyond middle of hindmargin,
feebly lunulate-dentate ; postmedian at nearly three-fourths, feebly or scarcely
lunulate-dentate, slightly inclining inwards costally, otherwise nearly parallel
with termen, the customary radial and submedian curves very gentle or scarcely
noticeable ; subterminal white line of medium thickness, sinuous or lunulate-
dentate, the grey shades on either side of it moderate or rather weak ; terminal
black dots small but well-developed, the anterior ones somewhat elongate, the
posterior smaller and more detached ; fringe slightly irrorated, with a clearer
white line at base. Hindwing rounded, scarcely bent at R1 ; first line wanting ;
median shade just proximal to (almost touching) the black cell-dot, which is
slightly less minute than on forewing ; the rest nearly as on forewing, but with
the postmedian rather more proximally placed.
Underside whitish, the hindwing almost unmarked, the forewing more
tinged with buff, especially anteriorly, and with minute cell-dot and weak,
buff-tinged postmedian line ; both wings with terminal dots present but weak.
Durban, Natal (G. F. Leigh). The type <$ in coll. Tring Museum.
A few §§ from Durban and other localities in Natal have been known to
me for several years, scattered in various collections, but I hesitated to describe
it, lest it might be a mere colour-form of nesciaria Walk, or latitans Prout ( =
reconditaria Snell., nee Walk.). The <$ structure, however, shows that it comes
nearer to spoliata Walk. ; differs in having the hindtibia rather thicker, tarsus
barely as long, antennal ciliation rather shorter, the colouring of the wings
different, the postmedian line even, not punctiform, the anterior terminal dots
elongate.
NOVTTATES ZOOLOOICAE XXVII. 1920. 309
21. Hamalia perbrunneata sp. nov.
cj, 19-21 mm. Closely allied to brunneata Warr. (Novitates Zoologicae,
xii. 322), structure nearly the same, though the hindtarsus may be a trifle longer
(well over one-half tibia, the first joint very slightly thickened, which is scarcely
appreciably the case in brunneata). Head and body coloured as in brunneata.
Wings brighter brown, less infuscated, the narrow dark borders and the terminal
blotches of forewing (between the radials and at tornus) consequently showing
up more distinctly.
Forewing with median shade slender (in brunneata thick), usually crossing —
in one example proximal to — the cell-dot ; postmedian line a little farther from
termen than in brunneata, less angulated at R1. Hindwing with termen
slightly less gibbous than in brunneata, postmedian line markedly farther from
termen.
Underside much lighter and less cupreous than in brunneata, especially on
the hindwing, which is, moreover, usually much less strongly marked ; post-
median line placed as above, on the hindwing less excurved behind middle than
in brunneata.
Pozuzo, Huanaco, E. Peru, 800 — 1,000 m., in various collections. Type
and others (W. Hoffmanns) in coll. Tring Museum. Also from Calama, Rio
Madeira, and from Charaplaya, Bolivia.
Has been mixed with brunneata Warr., of which the type from Cundimamarca
remains unique. I do not think it can be even a subspecies, but in any case
it must be named. The group to which these species belong differs from true
Hamalia in the stalking of SC! of the hindwing and in the genitalia, and will
require generic separation.
Genus Lobocleta Warr.
Lobockta Warr., Proc. U.S. Nat. Mus. xxx. 450 (1906).
Metasiopsis Prout, Tr. Ent. Soc. Lond. 1910, p. 219.
I think my Metasiopsis only differs essentially from Lobocleta Warr. in the
non-pectinate $ antenna, and should be regarded merely as a subgenus. It is
unfortunate that Warren mistook the bulk of this fairly extensive genus for
Ptychopoda and only established a new genus on a single aberrant member of it,
and almost equally unfortunate that in discovering the necessity for the generic
separation of the bulk I overlooked Warren's already existing name of Lobocleta.
22. Lobocleta xenosceles sp. nov.
c??, 21-22 mm. Face and palpus blackish, the latter pale beneath. Head
and body concolorous with wings, the collar brighter ochreous. Antennal ciliation
in $ slightly over 1, in $ minute. Midtibia in (J with a strong hair- tuft at end ;
hindtibia in $ dilated, rather elongate, with long strong hair-pencil (reaching
nearly to end of first tarsal joint) and a small additional hair-tuft at extremity ;
hindtarsus in <J abbreviated (less than half).
Forewing shaped about as in indecora Warr. (Novitates Zoologicae,
vii. 162) or malepicta Warr. (Novitates Zoologicae, xii. 46), colour intermediate
between these, rather glossy, without (or with only very sparse and minute)*
dark irroration ; markings about as in the species named, but, with the exception
310 NOVTTATES ZOOLOOICAE XXVII. 1920.
of the black cell-dot, always weak, sometimes almost entirely obsolete ; dots
of the postmedian line usually better developed, at least at costa ; fringe paler,
especially distally, marked at base with small black dots opposite the veins.
Hindwing with termen scarcely waved ; similar to forewing.
Forewing beneath with somewhat rosy flush, especially proximally, hindwing
whiter ; both very feebly marked.
Obidos, Amazons, October— November 1904 (M. de Mathan). Type <J and
allotype $ in coll. Tring Museum. Also in the same collection, ex coll. Meyer,
a (J labelled " Brazil " and 2 $, 2 $, merely labelled " S. America," all of which
may be suspected of coming from the Amazons, as was certainly the case with
many species in that interesting but badly localised collection.
23. Lobocleta unigravis sp. nov.
$, 19 mm. (Face abraded.) Palpus short, brownish, beneath white. Head
and body white, the body above with sparse black irroration ; collar tinged with
ochreous.
Forewing with termen gently curved, moderately strongly oblique ; SC!
from close to end of cell ; white, with sparse black irroration (slightly more
copious in proximal part of costal region) ; lines light ochreous brownish, the
antemedian, postmedian, and two subterminals weakly expressed, the median
rather stronger ; antemedian from about one-fourth costa, rather oblique outward,
sharply angulated in cell, then nearly straight to hindmargin before one-third,
dotted with black on SM* ; cell-dot rather large, sharply black ; median shade
just beyond it, obsolescent costally, angled outward on R1 and R3, incurved
between, oblique inward to hindmargin a little beyond middle, but slightly
angled outward on SM!, where it is accentuated by some black irroration ; post-
median and proximal subterminal approximately parallel with median but
more crenulate, more markedly angled outward on SM', the postmedian arising
from a rather noticeable black dot on costa and irrorated with black about SM! ;
distal subterminal close to termen ; black dots at vein-ends, the anterior ones
particularly strong. Hindwing not very long, termen slightly waved, rather
strongly gibbous, feebly bent at M> ; SC!— R1 stalked for about half their length ;
similar to forewing, the first line undeveloped, the median incurved proximally
to the cell-dot.
Underside with the cell-dots and the postmedian costal dot of forewing
strong, otherwise more weakly marked, the median and postmedian lines fairly
well developed, terminal dots nearly as above ; costal margin of forewing ochreous
brownish.
La Plata town. Type in coll. Tring Museum.
A very ordinary-looking little species, yet not particularly reminiscent of
any other. In some respects, though rather whiter, it somewhat recalls Scopula
albidulata Warr. (Novitates Zoologicae, iv. 432).
24. Ptychopoda subfervens sp. nov.
<J$, 20-25 mm. Very similar to fervens Butl. (7Y. Ent, Soc. Lond. 1881, 340).
Both the colours paler, the ground-colour being whitish lavender-grey, the
" red-brown " (burnt sienna or chestnut) markings more cinnamon-rufous.
NOVITATES ZOOLOGICAE XXVII. 1920. 311
Foreiving with costal edge less darkened than in fervens, remaining rufous ;
antemedian line usually more complete, more strongly bisinuate ; postmedian
different in form, being acutely angulated outward on R1, but less deeply incurved
behind M2 than in fervens ; the rufous band beyond not interrupted by the
ground-colour between the median veins ; subterminal line more sharply white ;
fringe paler. Hindwing with the markings in general weakly expressed, but
with a complete, well-defined white subterminal, which forms an acute, V-shaped
proximal projection on Rs.
Both wings beneath paler ; forewing somewhat darkened along costal
margin and with shadowy indications of the markings of the upperside ; hindwing
almost unmarked, with slight iridescence ; both wings with complete terminal
line.
St. Jean de Maroni, French Guiana, type o and others in coll. Tring Museum,
allotype 9 in coll. Dognin. Also from Juan Vinas (Costa Rica) and Potaro
(British Guiana), and a large, more ochraceous-marked $ from La Oroya, S.E.
Peru, which latter may perhaps eventually prove to represent a local race.
25. Ptychopoda palniensis sp. nov.
C?, 20-25 mm. Face black. Palpus black above, brown beneath. Vertex
whitish brown. Antennal joints triangularly projecting, ciliation nearly 2.
Thorax and abdomen concolorous with wings, collar brighter brown. Foreleg
(except tarsus) darkened on inner side. Hindtibia dilated, longer than femur,
fringed above and with long hair-pencil from femoro-tibial joint, tarsus extremely
short.
Forewing with areole moderately large, all the subcostals stalked beyond
it, SO separating just before SO ; brownish white, strongly irrorated with
slightly rufescent brown ; antemedian line not strong, obsolescent at costat
strongly excurved between SC and fold and more slightly behind fold, oblique
inwards to hindmargin ; cell-dot rather strong, black ; median shade obsolescent
at costa, rarely strong, touching the cell-dot on its distal side, scarcely incurved
posteriorly ; postmedian sharper, somewhat lunulate-dentate, the two customary
sinuosities ; distal area darkened, leaving free a slight streak from costa just
beyond the postmedian, a rather broad sinuous subterminal (formed nearly as
in the biselata group) and some slight terminal spots ; termen with blackish
interneural dashes ; fringe with small blackish dots opposite the veins.
Hindwing with termen waved and sinuous, slightly prominent at R1 — M1 ; first
line wanting, median proximal to cell-dot, postmedian little beyond centre, dark
borders sometimes vague.
Forewing beneath sharply marked, darkened to median shade, distal area
nearly as above, fringe paler proximally. Hindwing whiter, with strong black
cell-dot and rather weak brown median and postmedian lines ; terminal dashes
strong.
Palni Hills (W. H. Campbell). 5 $<$ in coll. L. B. Prout. Also in other
collections.
26. Cyllopoda janeira lugens subsp. nov.
Hindwing with the black abdominal and distal borders broader than in*
j. janeira Schaus (Proc. Zool. Soc. Lond. 1892, p. 286), and in addition with a black
312 NOV1TATES ZOOLOOICAE Xx VII 1920.
costal border above and beneath, which merely leaves free a slender, pointed
streak of the ground-colour at base. Forewing in general with the yellow markings
slightly reduced, as also the white scales at apex of fringe.
Castro, Parana (E. D. Jones). Type <J and 4 $$ in coll. Tring Museum.
Also in coll. E. D. Jones.
It seems that this is the " approximans " of Schaus and Warren, but not
of Walker.
Subfam. LARENTIENAE.
27. Lithostege buxtoni sp. nov.
cJ, 34 mm. Face blackish brown, paler in middle. Palpus short and
slender ; above dark, beneath pale. (Tongue concealed.) Antenna with fascicles
of rather long cilia. Vertex and body light brown. Foretibia with terminal
claws rather slender, the inner moderately long, the outer short.
Forewing rather narrow, costal margin faintly sinuous, apex round-pointed,
termen very oblique, gently curved posteriorly, tornus rounded off ; both areoles
ample, their dividing vein from apex of cell, SO, SO4, and SO from apex of distal
areole, R1 from beyond its middle ; very pale brownish with strong gloss (as in
Myinodes) ; an oblique dark line from apex nearly to hindmargin about 3 mm.
from base, consisting of a series of very shallow lunules separated by slight distal
and posterior indentations on the veins, slightly more longitudinal between M1
and M2 ; anteriorly to this line the colour is white for some distance, distally
and posteriorly slightly deeper brown ; fringe rather long, white, tinged proximally
with brown, a shadowy brownish line dividing the two colours. Hindwing
narrow and elongate ; C anastomosing with SC from near base to near end of
cell ; M1 separate ; glossy white.
Forewing beneath slightly more greyish, the line feebly showing through,
at least in apical part.
Kangavar, Hamadan, N.W. Persia, 5,000 feet, December 6, 1918 (P. A.
Buxton). Type in coll. L. B. Prout, kindly presented by the discoverer. A
second cJ, considerably darker and with the line more deeply lunulate-dentate,
has since come to hand from Mesopotamia (Shergat, Asshur, at light, December 27,
1919, H. D. Peile), and has equally kindly been presented to me by Mr. H. T. G.
Watkins.
According to the £ antenna, will require a new section of the genus. With
it will probably be associated — if my conjecture in Seitz, Macrolep. iv. 175 is
correct — the enigmatical chaoticaria Alph.
NOVITATES ZOOLOGICAE XXVII. 1920. 313
A NEW FAT-TAILED GEEBIL (PACHYUROM YS) FROM
WESTERN ALGERIA.
By Oldfield Thomas.
(Published by permission of the Trustees of the British Museum.)
AMONG the mammals obtained by Lord Rothschild's expedition into Western
Algeria in 1913, of which I gave a list in the Novitates,* there was a
young Pachyuromys from Ai'n Sefra provisionally determined as P. duprasi, the
Saharan form. But its colour was darker than one would have expected the
young of P. duprasi to be, and Lord Rothschild has since made efforts to get
further " Boubiedas " from that region.
Thanks to the help of M. Victor Faroult, he has now obtained three adult
skins from Mecheria, 100 km. north-east of Ain Sefra, and these he has kindly
placed in my hands for examination.
As I had expected from the colour of the young specimen, these adults clearly
represent a new and much darker form, which, at Lord Rothschild's suggestion,
I propose to name :
Pachyuromys duprasi faroulti, subsp. n.
Size and essential characters, including the skull and teeth, as in ordinary
P. duprasi of the Algerian Sahara. General colour, however, very much darker,
the back between " drab " and " buffy-brown," while duprasi is of a bright desert
colour, like other Gerbils of the same area. In addition, instead of the colour
passing without sharp line of demarcation into the white of the undersurface, the
line of division is quite sharply marked, and there runs along just above it a
broad band of bright " pinkish cinnamon," less developed on cheeks and flanks,
broad and conspicuous on the rump. Ears short, buffy whitish with their extreme
edges brown. Hands and feet wholly white as usual. Fine hairs of tail pale
cinnamon.
Dimensions of the type :
Head and bod3' (from skin), 105 mm. ; tail, 62 ; hindfoot, 23.
Skull, median length 33'2, greatest diagonal length to back of bulla 365 ;
condylo-incisive length, 30' 7 ; diagonal length of bulla, 17 ; bi-meatal breadth,
20 '5 ; upper molar series, 5.
Hab. Plateau of Western Algeria. Type from Mecheria, 1,100 m. ; another
specimen from Ai'n Sefra at the same altitude.
Type. Skin and skull. B.M. No. 20. 3. 1. 1. Collected in the summer of 1918
by M. Victor Faroult. Presented by Lord Rothschild. Four specimens in all.
The three forms of Pachyuromys now known present remarkably little differ-
ence in essential characters, either cranial or external, and should apparently
only be considered as local subspecies, of which those from Egypt and the
Algerian Sahara seem most nearly allied to each other.
* Nov. Zool. xx. p. 586, 1913.
314 Novitates Zoolooicae XXVII. 1920.
The three forms may be distinguished as follows :
A. General colour paler, passing gradually on sides into white of under-
surface, the line of separation not marked by a cinnamon band. Edges of ears
not darkened.
(a) General colour more or less ochraceous buffy. Algerian Sahara.
1. P. duprasi duprasi Lataste.
(6) General colour very pale yellowish buffy. Natron Valley, Lower
Egypt.
2. P. d. natronensis de Wint.
B. General colour darker, sharply demarcated on sides, and with a cinnamon
band along the lower edge of the upper colour. Extreme edges of ears brown.
Plateau of Western Algeria.
3. P. d. faroulti Thos.
Novitates Zoolooicae XXVII. 1920. 315
CAPTAIN ANGUS BUCHANANS AIR EXPEDITION.
I.
ON A SERIES OF SMALL MAMMALS FROM KANO.
By Oldfield Thomas and Martin A. C. Hinton.
T3 Y the kindness of the authorities of the Tring Museum we have been entrusted
-*—* with the examination of a number of small mammals obtained by Captain
Angus Buchanan, while stopping at Farniso, near Kano, North Nigeria (altitude
1,700 ft.), in December 1919, on his way to explore the unknown regions farther
north.
These Kano Mammals have proved to be of so much interest and to include
so many novelties that we have thought it worth while to give a complete list
of them.
The most striking form from a zoological point of view is undoubtedly the
little short-tailed Gerbil Desmodilliscus buchanani, which represents a genus
only discovered in 1917 and hitherto not included in the British Museum
collections.
The handsome little carnivore Poscilictis rothschildi is also a discovery of
some interest, as it greatly extends the known range of its genus, which has
only recently been distinguished from Ictonyx.
By the generosity of Lord Rothschild, a set of the species obtained by
Captain Buchanan, including the types of new species and subspecies, has been
presented to the British Museum.
The only place towards Kano from which the British Museum has hitherto
received any noticeable collection of mammals is the Bauchi Plateau, some
160 miles to the south-east, where the missionary brothers G. T. and J. C. Fox
collected a number which formed the basis of papers by Thomas in 1911-12.*
Practically all the species, however, prove to be different, and show that the
two places are in different faunal areas, of which Kano is strikingly more of a
desert character.
1. Hipposideros caffer tephrus Cabr.
6 28, $ 7.
Adults, in normal dark coat, agreeing in every respect with H. c. tephrus
as defined by Andersen (Ann. Mus. Genova [3], iii. p. 12).
Measurements of $ and $ : forearm, 46, 47 mm. ; metacarpal III, 33, 34 ;
ear, 13, 13 ; tail, 28, 25 ; hindfoot, 85, 8.
Skull No. 7 : length condyle to canine, 169 ; maxillary width, 58 ; canine
to m', 5-7.
* Ann. Mag. N. H. (8) vii. p. 457, ix. p. 209, and ix. p. 083.
316 NOVITATKS ZOOLOGICAE XXVII 1920.
2. Pipistrellus culex Thos.
<?5.
3. Poecilictis rothschildi sp.
$ 53. December 25, 1919. Type.
A small species with rather sharply defined coloration and a small black
tail-tip.
Size about as in P. multivittata. Fur thinner, less loose and fluffy, so that
as a consequence the black and white bands are more sharply defined, almost
as much as in true Ictonyx, from which we have recently separated Pcecilictis.
Black lines more absolutely black, less lightened by intermixed white hairs.
General pattern quite the same, the ^-shaped marking on the back with a well-
defined median black line. White frontal band much broader and more con-
spicuous, its breadth approximating to that of the black muzzle band in front
of it, and not much narrower than in the black crown band behind it. Below,
on cheeks and interramia it is quite continuous, and nearly equally broad. Ears
black with a very slight white edging at tip. Black bands on top of neck
continued forward to join the black crown patch ; not cut off at the occiput
as in other species. Belly with two inconspicuous rows of small white patches
running down the sides from the axillary to the inguinal region. Tail not very
bushy, mostly washed with white ; the terminal hairs tipped with black, as in
P. libyca, but the black far less in extent.
Skull about as in P. multivittata,, but rather more robust.
Dimensions of the type skin, measured in flesh :
Head and body, 222 ; tail, 126 ; hindfoot, 295 ; ear, 17.
Skull (not yet received from Capt. Buchanan).
A male skull sent home by Major Cock measures : condylo-basal length,
50 mm. ; zygomatic breadth, 30 ; interorbital breadth, Ho ; intertemporal
breadth, 115; mastoid breadth, 2V5 ; vertical height, including bullae, 21;
palatal length, 24. Length of p' on outer edge, 5' 9 ; transverse diameter of m1
54.
This little Zoril is a very well marked and striking species, and constitutes
a great extension of the range of the genus Poecilictis, the previously known
species occurring from Algeria to Suakin and the Upper Nile. Its original dis-
coverer was Major Hubert Cock, R.A., who obtained a specimen at Zungeru,
N. Nigeria, in 1904, but was only able to bring home the skull, which is now
in the National Museum and is measured above.
The genus Poecilictis has only been recently founded by us for the members
of the Ictonyx libyca group, these being distinguished from true Ictonyx by various
essential characters, of which the most noteworthy are the truncated skull,
hypertrophied bullae, and more hairy palms and soles. P. multivittata Wagn.,
referred to above, is better known as frenata Sund., but this latter name is certainly
a synonym of the former.
We have much pleasure in naming this very handsome little animal after
Lord Rothschild, by whom Captain Buchanan's expedition has been arranged, and
to whose generosity the National Museum owes a series of all the species obtained,
including the types.
Novitates Zoolooicae XXVII. 1920. 317
4. Taterillus gracilis angelus subsp. n.
c? 18, 19, 26, 40, 51, 58, 80 ; ? 35, 38, 52, 79.
Paler than true gracilis and with whitish head-markings.
Size as in true gracilis. General colour above more buffy, less ochraceous
than in that animal. In some instances this is not so marked on the back, but
the crown and forehead are in all cases of the paler and more buffy tint. Sides
of muzzle white nearly up to eyes. A linear area along above eye and extending
back to the ear-opening white or whitish, so that in upper view the whole frontal
area is bordered on each side with whitish. Ears buffy. Hands and feet pure
white. Tail very pale-coloured, generally whitish above, rarely rather buffy,
and white below to the tip, including the underside of the pencil.
Skull as in gracilis.
Dimensions of the type :
Head and body, 113 ; tail, 148 ; hindfoot, 29 ; ear, 19.
Skull, greatest length, 33 ; condylo-incisive length, 29 ; palatal foramina,
6-l ; upper molar series, 5.
Type. Young adult male, No. 51. Collected December 24, 1919.
Distinguished from true gracilis by paler colour and the whitish lateral areas
on the head.
5. Gerbillus nigeriae sp. n.
c? 48, 56, 57, 65 ; $ 24, 50, 55, 60, 62, 63, 64.
A small Gerbil allied to the Sudan G. agag.
Size about as in G. agag. General colour about normal Gerbil colour, not so
vivid as in the North Saharan G. gerbillus. Cheeks white, a lighter patch in front
of the eye, a more marked one behind it, and another behind base of ear. Ears
buffy. Fore-limbs white from elbow, hind- from ankle ; feet comparatively
short, soles hairy. Tail pale buffy above proximally, the rest white except that
there are a few brown hairs in the inconspicuous pencil.
Bullae small, about as in G. allenbyi and the small species of Dipodillus ;
much smaller than in G. gerbillus and its allies.
Dimensions of the type :
Head and body, 98 mm. ; tail, 108 ; hindfoot, 23 ; ear, 13.
Skull, greatest length, 28 ; condylo-incisive length, 243 ; zygomatic breadth
15'5 ; nasals, 107 ; breadth of brain-case, 13'2 ; anterior palatal foramina,
4-7 ; posterior palatal foramina, 26 ; bullae, 9x57; upper molar series, 4.
Type. Old female, No. 55. Collected December 25, 1919.
This pretty little Gerbil is no doubt closely allied to the G. agag of the Egyptian
Sudan, but has longer ears, a tendency to lighter patches in front of as well as
behind the eyes, and a buffy whitish instead of brownish upperside of tail, of
which the terminal tuft is less developed and has less brown in it.
6. Desmodilliscus buchanani sp. n.
$ 25.
Allied to D. braueri of the Egyptian Sudan, but with less enlarged bullae.
Size about as in D. braueri, or rather smaller. Fur very soft and fine.
318 NOV1TATES ZOOLOGICAE XXVII. 1920
General colour above sandy fawn, the sides little paler than the back, the fur
deep slaty blackish at base over most of the buffy area ; but in three nearly
equidistant regions, one below the ears, one in the centre of the flanks, and one
behind the hips, the slaty is absent, and the hairs are white with buffy tips.
Undersurface as usual wholly pure white. Cheeks, a prominent patch behind
the eyes, and another behind the ears white. Ears short, their proectote whitish
with black edges ; metentote blackish but with fine white hairs on it. Fore-
limbs and hindfeet white ; palms and soles apparently as described in D. braueri.
Tail little more than half as long as the head and body, thinly haired, not pencilled,
wholly white.
Skull on the whole not dissimilar from that of D. braueri, as shown in the
excellent figures published by Wettstein. The bullae are, however, a good deal
less swollen, especially anteriorly, where they do not nearly reach the zygomata,
nor surpass them laterally. Posterior palatal foramina even larger than in
braueri, exceeding in area the anterior pair.
Incisors exceedingly narrow, and so bevelled that the strongly marked
grooves appear laterally to be halfway along the outer side of the tooth ; front
surface white or whitish. Molars apparently very similar in structure to those
of D. braueri, except that the anterior lobe of m, is more or less median, instead
of diverging outwards. M3 wholly absent, as in D. braueri.
Dimensions of the type :
Head and body, 66 mm. ; tail, 37 ; hindfoot, 15 ; ear, 9.
Skull, greatest median length, 21 -4 ; condylo-incisive length, 20 ; zygomatic
breadth, 12p8 ; nasals, 7 ; interorbital breadth, 3'8 ; breadth of brain-case, 104 ;
bi-meatal breadth, 128 ; distance between bullae across interparietal, 6 ; palatilar
length, 9'3 ; anterior palatal foramina, 3'8 ; posterior palatal foramina, 2'9 ;
diagonal length of bullae, 9'8 ; front of meatus to back of bullae, 8'5 ; upper
molar series, 3'2.
Type. Young adult female, No. 25. Collected December 19, 1919.
This remarkable little Gerbil is a most valuable and acceptable addition to
the National Collection, as it represents one of the few genera that we had not
previously had. The original species was described by Dr. Wettstein * from
near El Obeid in the Egyptian Sudan, and this is clearly a second species of the
same genus, which is related to Microdillus, Desmodillus, and the other shorts
tailed Gerbils.
We have named it in honour of its captor, to whose interest in collecting
small mammals we are indebted for the many novelties contained in this Kano
series.
7. Steatomys cuppedius sp. n.
^ 36, 59; $ 39, 44, 61, 70.
A small species of the S. minulus group, with comparatively long tail.
Size about the same as in S. minutus and loveridgei, therefore much smaller
than the ordinary species allied to S. pratensis, and still more so as compared
with the only Nigerian species hitherto known, 8. caurinus. General colour pale
drab, without definite darkening on crown or middle of back, though of course
* Denkachr. Akad. Wise. Wien, vol. xciv. part ii. 1017, p. 115.
NOVITATES ZOOLOGICAE XXVII. 1920. 319
the sides are rather paler. Undersurface as usual white, the white area rising
well up on the cheeks, and taking in the whole of the forelimbs, but not the legs.
Ears of medium length, pale brown, a well-defined white spot at the base of their
outer edge, just below the meatus. Hands and feet pure white. Tail decidedly
longer than in minutus and loveridgei, almost wholly white, a few darker hairs
on the middle of its upper surface at base and tip.
Skull stoutly built ; bullae of medium size ; palatal foramina well open,
reaching backwards to the level of the middle of the first lamina of m1.
Dimensions of the type :
Head and body, 81 mm. ; tail, 42' 5 ; hindfoot, 135; ear, 13' 5.
Skull, greatest length, 217; condylo- incisive length, 20 4 ; zygomatic
breadth, 1T4 ; nasals, 8'6 ; palatilar length, 95 ; palatal foramina, 4'2 x 2"1 ;
upper molar series (worn), 3' 5.
Type. Female, No. 70. Collected December 29, 1919.
This Steatomys is readily distinguishable by its small size and comparatively
long tail. On the other hand, the species discovered by Mr. Fox on the Bauchi
Plateau — 8. cauriwus — is one of the largest of the genus, with a skull over 27 mm.
in length.
8. Arvicanthis sp.
<?21, 68 ; ?4, 71, 72, 76, 77.
A. testicvlaris group.
9. Rattus (Mastomys) sp.
<? 69 ; $ 47.
10. Rattus (Myomys) daltoni Thos.
3 8, 22, 31, 32, 42, 43, 46, 49, 75 ; ? 33, 37, 54.
The majority of these specimens are quite like ordinary daltoni, but three
of them, nos. 32, 46, and 49, are strongly melanistic, quite different from the
rest, and so like large examples of Mus musctdus that they were at first supposed
to be that animal, and then, on closer study, a special local blackish species.
But we have now no doubt that they really are melanos of R. daltoni, thus giving
an example of a somewhat rare phenomenon among wild Muridae, especially
among such as inhabit dry countries.
11. Leggada haussa sp. n.
<J 13, 14, 10, 17, 29, 45 ; ? 15, 49, 67.
A small pale gerbil-coloured species.
Size among the smallest of the genus. Fur crisp, not spiny, hairs of back
about 3 mm. in length. General colour above pale sandy or gerbil colour, not
far from " cinnamon-buff." Sides " light ochraceous-buff." Undersurface as
usual pure white, the white including the whole of the forearms, but a line of
buffy runs down the back of the legs to the ankles. Ears pale brown ; a distinct
white spot just below their outer base.
Skull of normal proportions ; palatal foramina long ; choanse not specially
contracted or pushed backwards. Molars of the highly developed Leggada type,,
with long anterior lobe to m1.
320 NOVTTATES ZOOLOQICAE XXVII. 1920.
Dimensions of the type :
Head and body, 55 mm. ; tail, 37 ; hindfoot, 115 ; ear, 95.
Skull, greatest length, 17; condylo-incisive length, 16"1 ; zygomatic
breadth, 9 ; interorbital breadth, 3"2 ; palatal foramina, 4 ; upper molar series, 3.
Type. Adult female, No. 67. Collected December 29, 1919.
This tiny mouse is related to the ordinary W. African L. musculoides Temm.,
but is decidedly paler in colour, and always has a distinct white spot at the base
of the ear.
NOVITATES ZOOLOOIOAE XXVII. 1920. 321
ON THE GENUS ELACHYOPHTHALMA Feld.
By Lord Rothschild, Ph.D., F.R.S.
THE genus Elachyophthalma was established by Felder in 1861 for a species
of the family Bombycidae. from Amboina which he called tricolor. Felder
placed the genus in the Saturnidae (Attacidae), although it struck him as very
aberrant, for he says in the footnote to the generic diagnosis, " Genus ab omnibus
Saturniidis jam habitu discrepans, Ocinarae Walker secundum alarum formam
fortasse accedens."
Its right place in the system is in the Bombycidae, immediately following
Gunda and Ocinara. The sexes are dimorphic and strangely different. The
(Jc? described in this article are described for the first time, all the hitherto
described specimens being $$.
The diagnosis of the genus, given by Felder, is as follows :
" Caput parvum, valde retractum. Oeuli minimi. Antennae (? nae)
breves, sat late pectinatae. Lingua nulla. Palpi minuti, caput aequantes.
Alae breviter ciliatae, integerrimae, anticae apice obtusae, margine externo
convexo, vena subcostali quinque-ramosa (ramo primo ad cellulae extimum
oriente), vena discoidali secunda fere in medio venae discocellularis arcuatae
oriente, ramis ultimis medianis approximatis, primo remotiore, posticae ro-
tundatae, vena costali ad basin cum subcostali connata, dein costae valde ap-
proximata, post hujus medium desinente, vena subcostali longe post cellulae
irregulariter clausae extimum ramificante, ramo tertio et secundo mediano
valde approximatis. Pedes breves, setosi, tibiae posticorum calcaribus duobus
apicalibus minutis. Abdomen ($ nae) subrobustum, alis posticis dimidio fere
brevius, ano subvilloso."
The synonymy of the genus is as follows :
Elachyophthalma Felder, Ber. Kais. Ak. Wiss. Wien (Math. — N.W. Class),
vol. xliii. (I) (25-44), p. 32 (1861). Type tricolor Feld.
Laganda Walker, List. Lepid. Ins. Brit. Mus. part xxxii. p. 389 (1865). Type
picaria Walk.
Diversosexus Bethune Baker, Nov. Zool. vol. xi. p. 402 (1904). Type bicolor
B. Baker.
There are two sharply defined groups of species : 1st, with the $9 more
or less golden yellow, resembling in general facies the genus Gunda, and with
the <J large with a diagonal orange band across the hindwings ; 2nd, with the
$$ black, white, and yellow, or black and white, or black and yellow, resembling
certain groups of Liparidae. and with the £ small and uniform brown. In the
latter group must be ranged two aberrant species, of which only $9 are known,
of a rufous-brown colour and mimicking almost exactly some species of the
Eupherotid genus Cotana. There are at present known 18 species, as follows :
1. Elachyophthalma megaxantha (Walk.).
Artaxa megaxantha Walker, List Lepid. Ins. Brit. Mus. part xxxv. p. 1913 (1866) (Batchian).
The type now in the Hope University Museum, Oxford, has remained unique.
21
goo Xovitaths Zoolooicae XXVII. 1920,
2. Elachyophthalma inturbida (Walk).
Leucoma inturbida Walker, List Lepid. Ins. Brit. Mus. part xxxii. p. 345 (1865) (Celebes).
This has also remained unique.
3. Elachyophthalma kebeae (B. Baker).
Gunda kebeae Bethune Baker, Novit. Zool. vol. xi. p. 370. No. 4. pi. iv. f. 32 (1904) (Mt. Kebea).
The series at Tring consists of 1 $ and 24 $?. The <J was hitherto unknown.
cJ. Pectus orange ; legs orange-yellow varied with maroon-chocolate ;
antennae chocolate-brown, pectinations no longer than in $ ; head, thorax,
and abdomen chocolate-brown.
Forewing maroon-chocolate-brown, disk sparingly sprinkled with yellowish
hairlike scales, an indistinct antemedial, strongly zigzag shadow band ; disco-
cellular stigma lunate black-brown ; a broad sinuate postmedian shadow band.
Hindwing maroon-chocolate-brown, inner one-third sprinkled with yellow hair
scales : a broad, oblique, wedge-shaped band of orange runs from base of wing
to termen between veins 4 and 6 ; a trace of a sooty line crosses the orange
before termen ; the hindwing is very long and ovoid.
1 J, 1 $ Mt. Goliath, Central Dutch New Guinea, 5,000 ft., March 1911 ;
1 $ nr. Oetakwa River, Snow Mts., Dutch New Guinea, October — December
1910 ; 6 $$ Kumusi River, N.E. British New Guinea, May 1907 ; 1 $ Good-
enough Island, 2,500 — 4,000 ft., April 1913 ; 1 $ Milne Bay, British New Guinea,
December 1898 ; 1 $ Lower Aroa River, British New Guinea, November 1904 —
March 1905; 1 $ Biagi Mambare River, N.W. British New Guinea, 5,000 ft.,
February 1906 (A. S. Meek coll.) ;— 6 $? Hydrographer Mts., N. British New
Guinea, 2,500 ft., March 1918 (Eichhorn Bros, coll.) ;— 2 $$ Dorey, Dutch New
Guinea, June 1 897 ; Kapour, S. W. Dutch New Guinea, January — February
1897 ; 2 $? Humboldt Bay, N. Coast Dutch New Guinea, September — October
1892 (W. Doherty coll.) ;— 1 $ Ninay Valley, Central Arfak Mts., Dutch New
Guinea, 3,500 ft., February— March 1909 (A. E. Pratt coll.).
The amount of dark scaling on the outer quarter of wings and the dis-
tinctness of the two transverse dark bands varies much in the $$, and two of those
from Kumusi River and one from the Hydrographer Mts. are practically pure
yellow. The Dutch New Guinea $$ appear to be generally smaller than the
rest, but two British New Guinea $$ are the smallest of all.
Length of forewing, tf 22 mm. ; expanse, 47 mm.
4. Elachyophthalma flava (Joicey & Talbot).
Gvnda kebeae flava Joicey & Talbot, Trans. Entom. Soc. Lond. 1910. p. 384 (Arfak Peninsula).
This is not a form of kebeae B. Baker, but a distinct . species easily
recognised by the brown apical area of the forewing and the cream-grey
tornal area of hindwing.
5. Elachyophthalma keiensis sp. nov.
$. Similar to kebeae but smaller, differs principally in having the legs golden
yellow instead of sooty black, and in the first 3 rings of the abdomen being strongly
suffused with yellow on the sides.
Novitates Zoological XXVII. 1920. 323
Length of forewing, 21 mm. ; expanse, 47 mm.
Hab. : 3 $$ Little Kei Island, March 1893 (H. Kiihn coll.).
6. Elachyopthhalma flavolivacea (Rothsch.).
Gunda flavolivacea Rothschild, Brit. Ornith. Union <k Woll. Exped., Lepid. p. 101. no. 552 (1915)
(Utakwa River).
1 $, type, Canoe Camp, Utakwa River, Dutch New Guinea, October 1912
(A. F. R. Wollaston) ; 4 $$ Upper Setekwa River, Snow Mts., Dutch New Guinea,
2,000—3,000 ft., August 1910 (A. S. Meek).
7. Elachyophthalma dohertyi sp. nov.
$. Head, thorax, and abdomen golden yellow. Forewing canary-yellow,
some irregular antemedian and cellular streaks, a postmedian line joining on to
the oblique apical one-third, the apical one-third of wing, and the margin dull
maroon- brown. Hind wings deep golden yellow.
Length of forewing, 17 mm. ; expanse, 37 mm.
Hab. 1 $ Tenimber Island, June-^July 1892 (W. Doherty).
8. Elachyophthalma meeki sp. nov.
$. Pectus and legs sooty brown ; head sooty brown ; antennae shafts
whitish, pectinations sooty brown ; thorax pale golden yellow ; abdomen sooty
grey- brown, anal tuft white on basal half, pale grey on apical half. Forewing
semi-vitreous pale golden yellow, apical one-third densely irrorated with grey
scales. Hindwing semi-vitreous pale golden yellow.
Length of forewing, 21 mm. ; expanse, 48 mm.
Hab. 1 § Angabunga River, affl. St. Joseph's River, British New Guinea,
6,000 ft. upwards, November 1904— February 1905 (A. S. Meek).
9. Elachyophthalma semicostalis sp. nov.
$. Pectus and legs sooty black-brown ; head sooty brown- black ; antennae
black ; thorax and tegulae orange-buff, rest sooty black-brown ; abdomen sooty
black-brown, anal tuft white. Forewing thinly scaled sooty black-brown, basal
half with an olive tinge ; basal three-fifths of costal area orange-buff. Hind-
wings basal two-thirds sooty black-brown, outer two-fifths orange-golden, fringe
black-brown. Underside basal three- fifths of forewing obliquely dull orange-
golden, outer two-fifths brown-black ; hindwing as above, but outer two-thirds
heavily dusted with dark scales.
Length of forewing, 22 — 26 mm. ; expanse, 48 — 58 mm.
Hab. 2 $$, type, Upper Aroa River, British New Guinea, February — April
1903; 1 $ Booboomie Aroa River, 2,000 ft., May 1905 (bred from cocoon) ;
1 $ Kumusi River, N.E. British New Guinea, July 1907 (A. S. Meek) ;— 1 $ Dorey,
Dutch New Guinea, June 1897 (W. Doherty).
The cocoon of this species is most curious ; it is flagon-shaped, quite hard,
and with a tail-like appendage 11 mm. long and dark brown in colour. It is
suspended free in the air by a cord 40 millimetres long attached to the underside
of a bamboo leaf.
324 Novitates Zoolooicae XXVII. 1920.
10. Elachyophthalma goliathina sp. nov.
(J. Dark chocolate-brown above ; an indistinct darker zig-zag antemedian
line and 2 darker serpentine zigzag postmedian lines more distinct on forewing ;
apex of forewing more olive. Hindwing with rufous tinge, abdominal margin
on edge with whitish lines.
Length of forewing, 26 — 28 mm. ; expanse, 56 — 60 mm.
Hah. 5 $$ Mount Goliath, Central Dutch New Guinea, 5,000 ft., February
1911.
11. Elachyophthalma tricolor Feld.
Elachyophthalma tricolor Felder, Ber. Kais. Ak. Wiss. {Math.—N.W. Class), vol. xliii. p. 32 (1861)
(Amboina).
6 $$, incl. type, Amboina (Doleschall ex coll. Felder) ; 5 $$ Amboina,
August 1892 (W. Doherty).
12. Elachyophthalma bicolor (B. Baker).
Diversosexus bicolor Bethune Baker, Novit. Zool. vol. xi. p. 403 (1904) (Dinawa) ($ descr. as <J ;
Baker's $ is a Lymantrid).
The amount of yellow at tornus of hindwings and the width and shape of
the median band of forewings varies very much.
5 $$ Milne Bay, British New Guinea, January — October 1 899 ; 1 ? Upper
Aroa River, British New Guinea, March 1903 ; Booboomie Aroa River, 2,000 ft.,
May 1905 ; 1 $ Goodenough Island, November 1896 ; 2 $$ Kumusi River,
N.E. British New Guinea, June 1907 (A. S. Meek) ;— 3 ?$ Hydrographer Mts.,
N. British New Guinea, 2,500 ft., April— May 1918 (Eichhorn Bros.).
13. Elachyophthalma melanoleuca sp. nov.
$. Legs, pectus, head, antennae, and thorax sooty black ; abdomen sooty
black, anal tuft white with bright buff centre. Forewing sooty black, a median
band broad, curved, white, reaching from inner margin to just below subcostal
nervure. Hindwing sooty black, a large, irregular, white triangular patch
extends from the abdominal margin to just above vein 5.
Length of forewings, 25 mm. ; expanse, 55 mm.
Hob. 3 $$ Humboldt Bay, September— October 1892 (W. Doherty).
14. Elachyophthalma insularum sp. nov.
<J. Uniform chocolate-rufous above ; sides of abdominal margin of hindwing
with oblique white streaks.
Length of forewing, 17 mm.; expanse, 38 mm.
Hob. 1 tf Roa Island, July 1897 (W. Doherty).
15. Elachyophthalma fergussonis sp. nov.
cj. Uniform chocolate-brown above ; thorax with a mauve-grey suffusion ;
forewings owing to the excavated termen strongly falcate ; hindwing tornus
much produced, 3 strong oblique white bands on abdominal margin.
Novitates Zoologicae XXVII. 1920. 325
9. Pectus, legs, head, antennae, and thorax sooty black-grey ; abdomen
sooty black, anal tuft buff-white below and on sides. Forewing sooty black-grey,
a broad creamy white curved band from subcostal nervure to vein 1 ; area
below vein 1 yellow on outer three-fifths. Hindwing basal two-fifths sooty
grey-black, outer three-fifths yellow, slightly sprinkled with dark scales ; fringe,
margin, and outer half of nervures sooty.
Second 9 has yellow below vein 1 of forewing and outer portion of hindwing
much obscured by black scales.
Length of forewing, $ 17 mm. ; expanse, 39 mm.
Length of forewing, 9 26 mm. ; expanse, 58 mm.
Hob. 1 <J, 2 99 Fergusson Island, December 1894 — November 1895 (A. S.
Meek).
16. Elachyophthalma iniraluteola sp. nov.
9. Pectus, legs, head, and thorax sooty brown-black ; abdomen sooty
brown-black, anal tuft buff-white on sides. Forewing sooty brown-black above,
with a broad curved white band. Hindwing above basal half except costa and
base pale golden yellow ; outer half, costa, and base sooty brown-black. Below
the white band on forewing is muchsextended.
Length of forewing, 23 mm. ; expanse, 51 mm.
Hah. 1 9 Humboldt Bay, N. Dutch New Guinea, September — October
1892 (W. Doherty).
17. Elachyophthalma doreyana sp. nov.
(J. Uniform rufous-chocolate above, a small yellow half-moon-shaped
discocellular stigma in forewing, and white streaks on abdominal margin of
hindwing.
9. Uniform sooty grey-black ; a broad white median band on forewing,
more even in width and more strongly curved than in bicolor B. Baker, tornal
half of abdominal margin greenish buff with black band across centre.
Length of forewing, <J 17 mm. ; expanse, 38 mm.
Length of forewing, 9 26 mm. ; expanse, 57 mm.
Hah. Dorey, N. Dutch New Guinea, June 1897 (W. Doherty).
Diversosexus aroa B. Baker is not an Elachyophthalma at all, but a Lymantrid
of the genus N'jgmia.
18. Elachyophthalma cotanoides sp. nov.
9. Pectus rufous-orange ; legs black, clothed on inner side with orange
hair ; antennae brown-black ; head and thorax rufous-orange ; abdomen
rufous-orange, anal tuft lead- blue at base, rest greyish white, centre rufous.
Forewing chocolate-rufous ; basal three-fifths of costal area orange, nervures
golden-yellow washed with rufous on inner four-fifths of wing, a darker rufous
and yellow double postmedian band, beyond which nervures broadly golden
yellow, a patch of golden buff between veins 2 and 4 on inner side of postmedian
band.
Hindwing chocolate-rufous, nervures on inner three-fourths slightly yellow,
NOVTTATES ZOOLOOICAE XXVII. 1920.
a somewhat obsolete postmedian band yellow, beyond which the nervures are
strongly golden yellow.
Below both wings chocolate-rufous, nervures strongly yellow.
Length of forewing, 25 mm. ; expanse, 56 mm.
Hab. 2 $$ Upper Setakwa River, Snow Mts., Dutch New Guinea, 2,000—
3,000 ft., August 1910 (A. S. Meek).
19. Elachyophthalma mimiocotana sp. nov.
?. Pectus and legs pale rufous washed with buff ; antennae chocolate-rufous ;
head and thorax pale rufous ; abdomen pale rufous, a transverse band and anal
tuft whitish. Forewing pale rufous, nervures golden buff, a patch occupying
most of cell and some indistinct marks below it golden buff, a chocolate-rufous
postdiscal band. Hindwing pale rufous nervures and broad postmedian band
golden buff.
Length of forewing, 21 mm. ; expanse, 47 mm.
Hab. 1 ? Lower Aroa River, British New Guinea, November 1904 — March
1905 (A. S. Meek).
NOVTTATE8 ZOOLOQICAE XXVII. 1920. 327
THE NEW NAMES IN J. HERMANN'S TABULA
AFFINITATUM ANIMALIUM.
By Dr. Erwtn Stresemann.
IN 1783 Johann Hermann,* Professor of Natural History at the University
of Strassburg, published a rather voluminous work entitled Tabula
Affinitatvm Animalium,^ in which an attempt at a natural classification of
vertebrates is made. J The birds are dealt with on pp. 131 to 235.
Hermann was exceedingly well acquainted with the scientific literature of
his time, and it might almost be said that his knowledge of birds was principally
derived from the works of his predecessors in ornithology. Among the books
quoted by him, BuSon's Histoire Naturelle des Oiseaux, 1 770-9, § stands in the
foremost rank. As every ornithologist knows, in that great work many repre-
sentatives of tropical bird-life were for the first time characterized under French
vernacular names. Hermann, an adherent of Linne's binomial system, thought
it advisable to propose for a good number of these novelties generic and specific
terms in the Latin language which are perfectly valid under existing rules, each
being accompanied by a reference to the particular species or group in Buffon's
work for which the new scientific term was intended. Some of these names have
undoubted priority over others in current use. Hermann, it must be remembered,
was the first author to introduce scientific designations for some of Buffon's new
species. Shortly afterwards a Dutch author, C. Boddaert, followed in his steps
by publishing the Table des Planches enluminees, now well known to ornithologists
through the reprint edited by the Willoughby Society. It has been pointed
out by C. W. Richmond j[ that Hermann's book has precedence over Boddaert's,
the latter having been issued " in December 1783 or later."
Owing to its scarcity, Hermann's Tabula Affinitatvm Animalium has been
rarely taken into account by ornithologists. The earliest reference I find is that
by Sclater,T( when quoting the generic name Myrmornis Herm. Several years
later Cabanis and Heine ** unearthed Hermann's specific name discolor, which
stood ever since for a Madagascar Roller of the genus Leptosomus ; while Rich-
mond called attention to Tinamus soui and the generic term Lybius. In
* A short biography of Hermann is to be found in R. Lauterborn's edition of L. Baldner's
Vogel,- Fisch- und Thierbuch, Ludwigshafen, 1903, pp. xxxviii-xxxix.
t Tabula | Affinitatum | Animalium | olim academico specimine edita | nunc | uberiore com-
mentario | illustrata j cum annotationibus | ad historiam naturalem animalium | augendam
facientibus | auctore | Johann Hermann — M.D. et Prof. | Argentorati 1783.
{ The tract " Tabula Affinitatum Animalium, Strassburg 1777," mentioned by Engelmann
and Carus, is a dissertation by G. Chr. Wiirtz, one of Hermann's pupils. This paper, consisting
of 1 6 pages in 8vo, contains no new names.
§ By a singular coincidence, Hermann's copy of that work, presented to him by Buffon's joint
author, Guenau de Montbeillard, and provided with numerous manuscript notes by his own hand,
passed into possession of the library of the Munich Museum, where it has been frequently consulted
by me while compiling the present article.
|| Auk 17, 1900, p. 179. A little-known memoir in which the author endeavours to determine
every bird figured in Daubenton's Planches enluminees is due to Heinrich Kuhl (Buffonii et Daubentonu
figurarum Avium coloratarum nomina systematica. Groningen, 1820).
% Proc. Zool. Soc. Lond. 1858, p. 270.
** Mus. Hein. iv. 1802, p. 57 (Anmerkung).
328 NOVITATES ZOOLOGICAE XXVII. 1920.
Ridgway's monumental work The Birds of North and Middle America, Hermannian
names are quoted in the synonymy of various species.
NEW GENERIC NAMES.
FORMICARIIDAE.
Myrmornis Hermann vs. Rhopoterpe Cabanis.
Myrmornis Hermann, I.e. pp. 188, 210, 235, proposed for " Fourmilier " of
Buff on, iv. p. 462. Type by tautonymy : " Le Fourmilier proprement dit "
of Buffon, iv. p. 473 = Formicarius torquatus Bodd. 1783. Replaces Rhopoterpe
Cabanis 1847. T}'pe by subsequent designation (Cabanis and Heine, 1859),
Formicarius torquatus Bodd.
CAPITONIDAE.
Lybius Hermann vs. Melanobucco Shelley.
Lybius Hermann, I.e. pp. 217/235. Type by monotypy, Lybius guifsobalito
Herm. 1783 (= Loxia tridactyla Gmelin, 1789). Replaces Melanobucco Shelley,
1889. Type by original designation, Bucco bidentatus Shaw, 1798.
SAGITTARIIDAE.
Sagittarius Hermann vs. Serpentarius Cuvier.
Sagittarius Hermann, I.e. pp. 136, 165, 235. Type by original designation:
"Sagittarius" Boddaert, Dierk. Mengehverk, vol. v. 1770, p. 17 = Falco ser-
pentarius I. F. Miller. Replaces Oypogeranus Borkhausen, 1797, and Serpen-
tarius Cuvier, 179S.*
NEW SPECIFIC NAMES.
FARADISAEIDAE.
Falcinellus fastosus (Herm.) vs. Falcinellus striates (Bodd.).
Promerops fastosus Hermann, I.e. pp. 194, 202, based on " Le Grand Promerops
a paremens frises " of Montbeillard, in Buffon, vi. p. 472, has priority over
Vpupa striata Boddaert, 1783.
DICAEIDAE.
Dicaeum australe (Herm.) vs. Dicaeum papuense (Gm.).
Pipra australis Hermann, I.e. p. 223, based on " Le Manikor " of Buffon, iv.
p. 431, takes precedence over Pipra papuensis Gmelin, 1789.
TANAGRIDAE.
Arremon taciturnus (Herm.) vs. Arremon silens (Bodd.).
Tanagra taciturna Hermann, I.e. p. 214 note, based on " L'Oiseau Silentieirx "
of Buffon, iv. p. 304, has priority over Tanagra silens Boddaert, 1783.
* Cf. C. W. Richmond, Proc. U.S. Nat. A/us. 53. 1917, p. t^.
NOVITATES ZOOLOGICAE XXVII. 1920. 329
ALAUDIDAE
Certhilauda eurvirostris (Herm.) vs. Certhilauda capensis (Bodd.) *
et Certhilauda africana (Gm.).
Alauda eurvirostris Hermann, I.e. p. 216, based on " Le Sirli du Cap de
Bonne Esperance " of Montbeillard, in Buffon, v. p. 65, antedates Alauda
ajricana Gmelin, 1789.
TYRANNTDAE.
Tyrannus eurvirostris (Herm.) vs. Tyrannus dominicensis (Gm.).
Sitta eurvirostris Hermann, I.e. p. 204, is based on " La Grande Sitelle a bee
croehu " of Montbeillard, in Buffon, v. p. 475, where we find Sloane's description
of an apparently young bird. The name antedates Lanius dominicensis Gmelin,
1788.
FORMICARIIDAE.
Myrmothera f campanisona (Herm.) vs. Grallaria brevicauda (Bodd.).
Myrmornis campanisona Hermann, I.e. p. 189 note, based on " Le grand
Befroi " of Buffon, iv. p. 470, antedates Formicarius brevicauda Boddaert, 1783.
Leucolepis arada (Herm.) vs. Leucolepis musica (Bodd.).
Myrmornis Arada Hermann, I.e. p. 211 note, based on " L' Arada " of Buffon,
iv. p. 480, antedates Formicarius musicus Boddaert, 1783.
Myrmotherula brachyura (Herm.) vs. Myrmotherula pygmaea (Gm.).
Muscicapa brachyura Hermann, I.e. p. 229 note, based on ' Le petit Gobe-
mouche tachete de Cayenne " of Buffon, iv. p. 554, and PI. Enl. No. 831, fig. 2,
antedates Muscicapa pygmaea Gmelin, 1789.
COTINGIDAE.
Procnias averano (Herm.) vs. Procnias variegatus (Gm.) et Procnias
nudicollis (Vieill.).
Ampelis Averano Hermann, I.e. pp. 211, 214, based on " 1' Averano " of
Montbeillard in Buffon, iv. p. 457 (based in its turn upon Marcgrave's " Guira-
punga"), antedates Ampelis variegata Gmelin, 1789. J
* Alauda capensis Boddaert, 1783, is preoccupied by Alauda capensis Linnaeus 1766 (Syst.
Nat. xii. p. 268, Alauda sp. 8), which has been generally overlooked (for instance, by Reichenow,
Vogel A/rikas, iii. p. 352).
t Myrmothera Vieillot, Anal, d'une nouv. Ornith. el. 1816, p. 43 : " Esp. Befroi, et quelques
autres fourmilliers de Buffon " ; type by monotypy : Myrmornis campanisona Herm. The generic
name Myrmothera is to be found in Vieillot's tract on the same page as Grallaria, hitherto used in
the same sense, but has precedence by several lines. — C. E. Hellmayb.
% Marcgrave's Guirapunga, the sole basis of both Ampelis averano Herm. 1783 and Ampelis
variegata Gmelin {Syst. Nat. I. ii. 1789, p. 841), had hitherto been referred to the Black-winged
Bell-bird of British Guiana, Trinidad, and Northern Venezuela. Although — as pointed out long
ago by Lichtenstein (Abhandl. Berliner Akad. a. d. Jahren 1816-17, publ. 1819, p. 163) — Marcgrave
(Hist. Nat. Bras. p. 201) described a bird in change from juvenile to adult plumage, there can be
hardly any doubt as to its having belonged to Procnias nudicollis (Vieill.), the only species of Bell-
bird occurring in Eastern Brazil. In spite of the fact that Marcgrave's account is in several respects
330 NOVITATE8 Zoolooicae XXVTT. 1920.
Procnias alba (Herm.) vs. Procnias nivea (Bodd.).
Ampelis alba Hermann, I.e. p. 213 note, based on " Le Guira Panga ou
Cotinga blanc " of MontbeiLlard, in Buffon, iv. p. 454, antedates Ampelis nivea
Boddaert, 1783.
CAPITONIDAE.
Lybius guifsobalito Herm. vs. Melanobucco tridactylus (Gm.).
Lybius guifsobalito Hermann, I.e. p. 217 note, based on " Le Guifso Balito "
of Buffon, iii. p. 471, is much earlier than Loxia tridactyla Gmelin, 1789.
CORACIIDAE.
Coracias abyssinicus Herm. vs. Coracias abyssinus Bodd.
Coracias abyssinica Hermann, I.e. p. 197, based on " Le Rollier d'Abyssinie "
of Montbeillard, in Buffon, iii. p. 143, antedates Coracias abyssinus Boddaert,
1783.
ALCEDINIDAE.
Dacelo novaeguineae (Herm.) vs. Dacelo gigas (Bodd.).
Alcedo novae Guineae Hermann, I.e. p. 192 note, based on Daubenton's
PL Enl. No. 663, antedates Alcedo gigas Boddaert, 1783.
CAPRIMULGIDAE.
Chordeiles acutipennis (Herm.) vs. Chordeiles acutipennis (Bodd.).
Caprimulgus acutipennis Hermann, I.e. p. 230 note, based on " L'En-
goulevent acutipenne de la Guyane " of Montbeillard, in Buffon, vi. p. 547,
antedates Caprimulgus acutipennis Boddaert, 1783.
MICEOPODIDAE (Apodidae).
Chaetura martinica (Herm.) vs. Chaetura acuta (Gm.).
Hirundo martinica Hermann, I.e. p. 229 note, is based on " L'Hirondelle
a queue caree de la Martinique " of Montbeillard, in Buffon, vi. p. 553, who
refers to " L'Hirondelle de la Martinique " of Brisson, Ornith. ii. p. 499. The
name has priority by several years over Hirundo acuta Gmelin, 1789.
CUCXTLIDAE.
Saurothera longirostris (Herm.) vs. Saurothera dominicensis Lafr.
Cuculus longirostris Hermann, I.e. p. 186, based on the " Tacco " of Mont-
beillard, in Buffon, vi. p. 402, antedates Saurothera dominicensis Lafresnaye, 1847.
incorrect {e.g. he erroneously took the bristle-like feathers on the naked throat for fleshy wattles !),
the name .4. averano cannot well be avoided as being the oldest for the East Brazilian Bell-bird
and must be used in place of P. nudicollis (Vieill.) 1817, of which A. variegata Gmelin becomes likewise
a synonym.
P. variegata auct. (nee Gmelin) is entitled to the name Procnias carnobarba (Less.), since Lesson
{Traile d'Orn. livr. 5, end of 1830, p. 3t>5, pi. 52, fig. 1) described and figured 8. n. Averano carnobarba,
an adult male secured by Robin on the island of Trinidad. A little-known synonym thereof is
Procnias lumbriciferus Gistel (in Gistel and Brommet Handb. Naturg. alter drei Reiche, Stuttgart.
1850, p. 295 : " in Waldern Brasiliens," errore !), accompanied by an excellent description of both
sexes. Neither of these names is mentioned in the synonymy of 0. variegata in Volume xiv. of
the Catalogue oj Birds in the British Museum. — C. E. Hellmayb.
NOVTTATES ZOOLOOICAE XXVTI. 1920. 331
OTIDIDAE.
Houbaropsis indica (Herrn.) vs. Houbaropsis bengalensis (Gm.).
Otis Indica Hermann, I.e. p. 138, based on " Le Churge ou l'Outarde moyenne
des Indes " of Buffon, ii. p. 56, antedates Otis bengalensis Gmelin, 1789.*
SYNONYMS OF HERMANN.
Gracula Martinus Hermann, I.e. p. 195 note, ex Buff. iii. p. 423, " le Martin "
= Acridotheres tristis (L. 1766).
Paradisaea sexfilis Hermann, I.e. p. 166, ex Buff. iii. p. 171, " Le Sifilet
ou Manucode a six filets " = Parotia sefilata (Penn. 1781).
Lanius Gonolek Hermann, I.e. pp. 179-180, ex Buff. i. p. 314. " Le Gonolek "
= Laniarius barbarus (L. 1766).
Oriolus albistriatus Hermann, I.e. p. 204 note, ex Buff. iii. p. 197, " L'Etour-
neau des terres Magellaniques ou le Blanche-Raie " = Trupialis militaris
(L. 1771).
Oriolus striatus Hermann, I.e. p. 204 note, ex Buff. iii. p. 265, " Le Loriot
raye " (based in its turn upon Brisson, ii. p. 332, " Le Loriot a teste rayee ")
is indeterminable. It invalidates the later Oriolus striatus Quoy and Gaim.
1830, which has to bear the name Oriolus grand (Mathews) (Ibis, 1916, p. 297).
Loxia jusca Hermann, I.e. p. 221 note, ex Buff. iv. p. 388, " Le Bouveron "
= Sporophila lineola (L. 1758).
Loxia flabellicauda Hermann, I.e. p. 186, ex Buff. iii. p. 463, " La Queue
en Eventail " = Guiraca caerulea (L. 1758).
Fringilla ministra Hermann, I.e. p. 220 note, ex Buff. iv. p. 86, " Le Ministre "
= Cyanospiza cyanea (L. 1766).
Loxia scandens Hermann, i.e. p. 216, ex Buff. iv. p. 398, " L'Hambouvreux "
= Passer montanus (L. 1758).
Pipra longicauda Hermann, /ex Buff. iv. p. 429, " Le Plumet blanc " =
Pithys albifrons (L. 1766).
Tanagra Misisippica Hermann, I.e. p. 214 note, ex Buff. iv. p. 252, " Le
Tangara du Mississipi " = Piranga rubra (L. 1758).
Tanagra mancipium Hermann, I.e. p. 211 note, ex Buff. iv. p. 263,
" L'Esclave " = Dulus dominicus (L. 1766).
Larus maximus Hermann, I.e. p. 146 note, description of a Herring-Gull,
captured in the neighbourhood of Strassburg in September 1772 = Larus
argentatus Pont. 1763.
Emheriza Mytilene Hermann, I.e. p. 222 note, ex Buff. iv. p. 322, " Le
Mitilene de Provence " = Emberiza rustica Pall. 1776.
Motaeilla pyrenaica Hermann, I.e. p. 226, based on the " Pegot," excellently
described by de Lapeirouse in Rozier's Observations sur la Physique, xiii. 1779,
pp. 422-4 == Prunella collaris collaris (Scopoli, 1769) ex Pyrenaicis montibus.
Psittaeus Arimanon Hermann, I.e. p. 182, based on the " Arimanon " of
Buffon, vi. p. 175= Coriphilus peruvianus P. L. S. Muller, 1776.
* Otis indica Herm. 1783 precludes the further usage of Otis indica Gmelin, 1789 (Syst. Nat-
I. ii. p. 725), for which the next available name is Otis aurita Latham (Ind. Orn. ii. 1790, p. 660).
The species has therefore to stand as Sypheotis aurita (Lath.) in place of S. indica (Gm.).
332 Novitates Zoolooicae XXVII. 1920.
Anas melanocephala Hermann, I.e. p. 161 note, description of a specimen
which had been ascertained by dissection to be a male, captured in January 1774
(near Strassburg ?) = Bucephala clangula (L. 1758), description of a male in
juvenile plumage.
Anas Leucotis Hermann, I.e. p. 161 note, description of a specimen actually
examined by the author = Nyroca marila (L. 1761), description of the female.
Alcatras Hermann, I.e. pp. 155, 235, is based on the " Alcatraz " in Rozier's
Observations sur la Physique, xiv. 1779, p. 475. The description of that bird,
" translated from the Italian," appears to have issued from the pen of G. % Molina.
This author gives Alcatraz as the Spanish name of Pelecanus Thagus Molina.*
Alcatras Hermann, 1783, becomes, therefore, a synonym of Pelecanus Linnaeus,
1758 ; its type is Pelecanus thagus Mol.
* Cf. Molina, Saggio eulla storia naturale del Chili, 1782, p. 240.
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PAGES
1. SPHINGIDAE OF PARA (Pis. I— XI) . . A. Miles Moss . . 333—424
2. TYPES OF BIRDS IN THE TRING MUSEUM Ernst Hartert . . 425—505
3. A NOTE ON TYPE-LOCALITY AND GEOGRA-
PHICAL RACES OF THE GUNDI (CTENO-
DACTYLVS GUNDI ROTHM.) . . . Oldfield Thomas . 506—507
4. SUPPLEMENTARY NOTES ON DIOPTIDAE . Louts B. Proul . . 508—509
5. ON SOME AFRICAN SPHINGIDAE (Illus-
trated) KarlJordan . . 510 — 512
NOVITATES ZOOLOGICAE.
Vol. XXVII. NOVEMBER 1920. No. H.
,A$ SPHINGIDAE OF PARA, BEAZIL.
EARLY STAGES, FOOD-PLANTS, HABITS, ETC.
By the Rev. A. MILES MOSS, M.A., F.Z.S., F.E.S., British Chaplain of Para.
(Plates I-XI.)
INTRODUCTION.
rpHE present treatise, though published under the auspices of Lord Rothschild
-L and Dr. Jordan in the Novitates Zoologicae of Tring, must be regarded
as a sequel and continuation of my Sphingidae of Peru, produced by the
Zoological Society of London in their Transactions for 1912 (vol. xx part ii
No. 1).
It was due to the warm appreciation of the results of my self-imposed task
on the part of certain entomological friends in Tring and London that this small
work was privileged to see the light. My information at that time was
accumulated during a three years' sojourn in Lima, from which I made occasional
expeditions over the Andes into the hilly, well-watered, and thickly-forested
region of the Interior as far as the river Perene. The volume comprises notes
relating to 47 species, with many coloured figures of the early stages of some
22 which had come under my direct observation and been verified, together with
a map of the limited district which I had the opportunity of exploring. The
investigation of the early stages of Lepidoptera in general has for many years
been to me the special charm of collecting, even in England, where, by comparison
with distant Peru and other parts of the tropics, almost everything relating to
larvae and food-plants is already known. An opposite state of things, however,
prevails in S. America, where the large majority of its splendid butterflies and
moths are known only as regards general locality in the winged condition. Little
by little, at any rate, the different species of kindred or widely-separated groups
have been falling into line ; and though in so vast a field of research the work of
an individual for a lifetime can never be more than a measured contribution, I
am now in possession of voluminous notes and figures relating to the larvae and
pupae of Papilios, Morphos, Caligos, other butterfly genera such as Heliconius,
Danais, Ithomia, Prepona, Calonephele, Ageronia, etc., the Notodonts with their
wondrous diversity in larval form, the Bombyces, Saturniidae, and Limacodidae
with their extraordinary spined and stinging caterpillars ; and last, but not
least in interest, tfte elegant and highly-developed Sphingid family.
22
334 Novitates Zoolooicae XXVII. 1920.
My hunting-ground, though remote from the former, and separated from
it by some 3,000 miles, is nevertheless part of the same continent, and possesses
a climate and a vegetation widely different from the Pacific Coast, but not
altogether dissimilar from the Interior of Peru. The continuity, therefore, of
my former investigations has been emphasized by the recurrence of species of
wide distribution, and this to an even larger extent than I had anticipated.
Common insects among the Hawk-moths, like Herse cingulata, Pseudosphinx
teirio, Eriinnjis ello, etc., are known to have an enormously wide range in
the American continent, reaching in some instances from Canada to Argentina,
and from the Pacific Ocean to the Atlantic, inclusive of the West Indian Islands ;
but I have been not a little surprised, when tabulating my Para species, to renew
acquaintance with so many old friends. In Sphingidae alone I find that no
fewer than 25 out of the 47 Peruvian species occur here in greater or less abund-
ance. Now, after some eight years' residence in the immediate vicinity of the
city of Belem (Para), my total list of Hawk-moths has just reached 90 distinct
species — a remarkable number when contrasted with the mere 30 which the
climate of Europe can support, or the 912 or so known to the entire world. In
addition to the 22 species of which I have been fortunate enough to find the
larvae, figure them, and more or less study their habits and food-plants according
to the opportunity, 17 of this number being common to Para, I am now similarly
informed in regard to at least 46 other species, not hitherto obtained or remaining
unidentified. The larvae, generally at full growth, sometimes also in the earlier
instars, together with a few characteristic pupae, have been figured life-size in
water-colours, with all the patient care and faithfulness to detail which I could
command in the matters of size, form, and colour. The pupae in many
instances throughout an entire genus, such as Xylophanes, approximate to a
certain standard or generic pattern, and the highly-important differentiating
characters between allied species, such as those supplied by the form of the
cremaster, are too minute to portray except by photography or by enlarged
diagrams. For other reasons I have been obliged largely to eliminate the
portrayal of the food-plants.
Judging by numbers alone it would seem that Para is by far the richer
field for Sphingidae, and this of course is true if balanced against Lima, which
is merely an oasis of green on a desert coast.
But when a comparison is made between the mouth of the Amazon and
its head-waters in the region of Chanchamayo and Perene, it is by no means so
easy to form a just relative estimate. Wallace and Bates discovered many
butterflies in Para, but they never even saw many of the Hawk-moths which I
find commonly here, and for the simple reason that in their day there were no
electric arc lamps to attract them.
There are none in the wild Interior of Peru to-day, and the wonder is, looking
back at those hasty mule-back trips of ten days at a time, and not always at
the best time, that one caught so much. Except for stray moths taken by
day, or subsequently bred from larvae on those rare occasions when all con-
ditions were favourable, the only attraction after dark in those parts was a
solitary kerosene lamp.
Here, in Belem, conditions are very different : we live in the midst of swamp
and forest unending, 100 miles from the open sea, with the great muddy, tidal
river in front of us, intersected by innumerable islands, and each one clothed to
NoyiTATEg Zoologicae XXVII. 1920. 335
the water-line by an impenetrable tangle of trees and creepers. We live also in
a blaze of electric light nowadays, and from far and near come the moths under
the baneful influence of our nightly illuminations ; and this to such an extent
that what was once superabundantly common when the electric plant was first
installed about 1895, is now comparatively rare, through a process of decimation,
as I suppose, within the area of light's attraction. Whether my explanation
is adequate to account for the diminution I cannot say for certain, but many
bear witness to the fact that there has been an obvious decrease in the
number of corpses beneath every brilliant arc lamp since 1908, when the road-
cleaners would sweep them up by the bin-full at a time.
It is true that Erinnyis ello is still so common in the early months of some
years, that on certain occasions it is no exaggeration when I say that I have
counted over 200 at a single lamp. Thick, like a swarm of bees, they definitely
obscure the light as they swirl around the globe or momentarily settle upon it.
The insulated wires are practically invisible, so thickly are they coated with
moths, giving them the appearance of being tattered to rags. On every adjacent
object does ello settle, walls, palings, tree-trunks, foliage, and even human beings,
while many lie squashed on the pavement beneath the feet of pedestrians or by
vehicles in the road. Of no other species, however, in these parts can the same
be said ; and having now lived in Para for considerable periods on and off since
1911, and having worked the lamps at all times of year and searched every
available part of the matto surrounding the city for larvae and imagines, I have
come to the fixed conclusion that we possess an immense and extensive ento-
mological fauna, corresponding to the vegetation, but that hardly anything is
really abundant. Species in plenty but paucity of individuals is a characteristic
of Belem, as opposed to other parts of the States of Para and Amazonas up-river,
where butterflies like the Pieridae, for example, may sometimes be caught,
40 or 50 at a single stroke of the net.
These remarks apply with special force to such families as the Erycinidae
among the butterflies, and to the Syntomidae, Limacodidae, and Notodontidae
among the moths, and they are no less applicable to the Sphingidae. Statistics
in the matter of relative abundance are apt to be erroneous and to defy conclusions,
but my experience seems to suggest a fairly equal grouping of the Para
Sphingidae under four heads, as follows : Single specimens or very rare ; rare
or of spasmodic occurrence ; hidden but not rare ; common and occasionally
abundant ; about 22 in each group.
It is worth while to examine, and as far as possible to co-ordinate, the various
causes which make for the abundance or scarcity of particular species ; for
apart from the disturbance of nature's balance by the introduction of brilliant
and attractive lights, for which man is responsible, there are many important
factors over which he has little or no control, and which claim the attention of
every observant person.
Let us consider first the species which are abundant, and see why this is
probably the case. Our conclusions "rank under three heads :
( 1 ) General hardiness and adaptability of larva to withstand various
climates and thrive on various food-plants.
(2) The abundance and wide distribution of suitable plants.
(3) The comparative or total absence of parasitic attack.
All these conditions appear to be fully satisfied in the case of ello, which is
336 Novitates Zoological XXVII. 1920.
doubtless the commonest Sphinx hi the American continent, and so can still
afford, better than any other, to lose a few millions periodically at electric lamps.
Only once in numerous examples have I found it affected by dipterous parasites.
The next point to notice is that Euphorbiaceae, with which the larva is chiefly
associated, is an immense and widely-distributed Order of plant-life, and also
that ello largely facilitates matters for itself by being able to feed freely on very
many species belonging to different genera of that order. My idea, in short,
then, is that the insect is hardier, and has a wider range of distribution, than any
one species of those plants which sustains it as a larva ; and as one after another
fails when the tropics are exchanged for the colder regions, its place is taken by
some other plant which provides an equally nutritious pabulum. The chief
means of sustenance in the Para region for ello are apparently two in number,
the rubber tree (Hevea brasiliensis), for which Para is famous, and the mandioca
[Manihot utilissima), for which it is hardly less so, providing, as it does, the
native substitute for bread and starch from here to the coast of Peru. Even
with this abundance others are occasionally preferred, and thrice, to my surprise,
have I discovered ello associating itself with the entirely distinct Order Sapotaceae,
and feeding on the leaves of " abiu " (Lucuma caimito). In two of these cases,
being half-grown, the larvae stoutly refused to eat anything else. One died
of starvation through my too-prolonged experiment with other leaves ; with
the other I gave way, hoping that possibly I had discovered the larva of E.
lassauxi, a totally distinct creature associated with Asclepiadaceae, but this I
only learnt three years later. It was carefully figured to note subtle points of
difference, but on emergence, to the banishment of my hopes, it produced but
a perfect and typical ello. In Barbados ello feeds on the deadly " manchineel "
(Evphorb.) ; and in the Lima district it was more often found feeding on
Euphorbia pilvlifera and heterophylla, Cnidoscolus fragrans, Cvrcas piirqans,
and Poinsettia pulcherrima.
Continuing this line of research, we pass briefly to such common and widely-
distributed species as Herse cingulata, the Convolvulus Hawk of America, the
larvae of which thrive equally well on the cultivated sweet potato of these parts,
with its abundant wild variety called " salsa," as they do on any species of
true bind-weed from north to south and right across the continent. This species,
again, seems to enjoy complete immunity from parasitic attack.
A few other examples may be cited, e.g. Protoparce sexta, a Solanaceous feeder,
which is very widespread, and is as .much at home on the potato and tomato of
North America as it is on the tobacco, the capsicum peppers, or the " jurubebas "
of hotter parts. Within the great Order of Solanaceae, though more especially in
the genus Solanum, there is never the lack of appropriate fodder ; and once
again I have only occasionally found this species troubled with dipterous and
hymenopterous parasites. Pseudosphinx tetrio, an Apocynaceous feeder, though
limited to Plumiera, is never at a loss in establishing a large gregarious brood
of larvae, which will as readily defoliate the Frangipanni trees adorning the
gardens of the West Indies and Brazil as the many still undescribed species of
that genus, known here as " sucuuba," and ranging throughout all the more
open parts of these tropical forests. Never have I discovered any parasite
which attacks this most showy and abundant caterpillar.
Pachylia ficus, another very common and widely-distributed species
associated with Moraceae, I recall for the particular purpose of showing
Novitates Zoolooicae XXVII. 1920. 337
that her adaptability to environment gives us at least one of the causes
of her abundance, and affords a fine example of the working of an unerring
instinct in regard to the distribution of her ova. I have learnt some botany
from her at first-hand, and also a new riddle, which I may perhaps be pardoned
for quoting as a good instance of appearance deceiving the eye, viz. — When is
a willow tree not a willow tree ? — When it is a ficus ! Such a tree grows in our
Botanic Garden in Para, and was at first quite erroneously recorded by me as a
Salix. After repeatedly finding the caterpillar of this species on it and on many
other trees of very distinct form and foliage, if I have not yet learnt how many
different species of Ficus there are, I at least realize how deep and sound were
the lines of our scientists, who, under the titles Moraceae and Urticaceae, were
bold enough to group with Ficus such dissimilar trees as Artocarpus and Cecropia.
On representatives of all three genera the larvae of Pachylia, especially P. syces,
are often found feeding.
My friend and botanical instructor of former days in Para, Dr. Huber of
the Museu Goeldi, and a botanist of the very first rank, was greatly impressed
with this interesting sidelight on our parallel studies.
In their own limited degree, and in accordance with their particular needs,
there are no finer botanists in the world than the moths, nor any such savants
in the minute details of organic chemistry ; for, by methods beyond our com-
prehension, they know exactly where to lay their eggs, and of what particular
shade of composition those leaves must be to admit of nourishing their progeny,
or of even providing them with their first green meal. P. ficus is sometimes, but
rarely, stung by the same small hymenopterous fly which, in Para, too frequently
brings about the destruction of its congener, P. syces.
We have instanced enough by way of example, taking a few of the commonest
species, to show, I hope correctly, why they are common.
Everything is a matter of degree, and the conditions, favourable or un-
favourable to the life of a species, would appear to differ in every case. In
regard to the scarcity of many species, I have occasion throughout to point to
causes which are traceable, and which, whether acting singly or in combination,
are obviously enough to bring about the rarity of rare species, and reduce others
to well-nigh the point of extinction.
Before, however, considering these causes, there are other points in regard
to abundance and wide distribution of which we must take account. The first
is that such species as ello, cingulata, sexta and tetrio among those instanced, as
well as many other moderately common forms like Pholus labruscae, are known
to be long and strong fliers, as evidenced by their capture at sea and on the
cold inhospitable heights of the Andes, far away from the localities and plants
which gave them birth. This propensity of wandering, though it must result
in the destruction of scores of individuals, betokens an extraordinary power of
endurance, and exhibits an inborn tendency to spread and to establish when
conditions are favourable. That this has been the case with many, one cannot
doubt ; that it fails of its purpose in other instances, and more by faulty climatic
conditions than by any shortage of food, is equally apparent. This is well
illustrated in the case of P. tetrio, which was sometimes intercepted in its long
flights over the Andes by the electric lights of Cerro de Pasco at an altitude of
nearly 15,000 feet above sea-level, but which also frequently reached the coast
from the Interior. There in the neighbourhood of Lima, the Frangipanni, its
338 NOVITATES ZOOLOGICAE XXVII. 1920.
food-plant, was common in gardens, but the conditions were chill and gloomy,
and never once could I discover its very obvious and easily-found larva, or
induce a captured female to lay eggs.
In England, to take a parallel case, we never tire of regretting that Euphorbia
on the south coast and Galium on the sandhills of Lancashire are not enough
in themselves to induce the lovely Celerio euphorbiae and C. gallii to take up their
residence among us permanently.
Returning to the question of abundance, an important feature to note is
the greater hardiness sometimes observable in the larvae of many common species
over rarer forms, the latter appearing to be more delicate and fastidious and
susceptible of attack. Often have I noticed that a rare species, though provided
with suitable food, will in many cases absolutely refuse to eat, if sealed up within
the confines of a biscuit-tin ; whereas common things like sexta will finish off
every scrap of leaf and stalk, and manage to pupate somehow, though deprived
of nature's bounty. Fortunately, nature can provide no such harsh parallel,
but even in the wild state caterpillars, like other creatures, have troubles many
and various to meet ; and the extra degree of hardiness to withstand every wind
that blows may quite conceivably spell the salvation of the individual and
the increase of its kind.
The percentage, too, in the death-rate of pupae, considered in relation to
the brevity or longevity of the pupal period, is another factor of importance
to note. Under artificial conditions this is certainly a very variable quantity
with different species, but for that very reason it is difficult to generalize and to
say exactly what happens in nature, for better or for worse. Undoubtedly here,
as with larvae, some are more delicate, and are more readily influenced for weal
or woe than others by conditions of humidity and temperature.
The last point I wish to make in connection with the abundance of those
species which we have been considering, and many others almost equally common,
is that in proportion as they are common, due allowance being made for the
limitations imposed by climate, range and extent of food-plant, general hardiness,
etc., so are they comparatively free, not from outside foes, but from that still
more serious and deadly complaint, parasitic attack in the early stages, which
is generally irremediable. By this I do not, of course, mean that their abundance
gives them any such immunity, but that the immunity which they enjoy in
this respect is at least one of the prime causes of their abundance. This I take
to be a most important consideration, and though even here there are exceptions,
I am convinced that the converse is equally true, viz. that the rarity of many
rare species, where the struggle for existence is obviously very severe, is primarily
due to excess of parasitic attack in the early stages of those species. Doubtless
all this is governed by the laws of nature, and summed up under the principle
known as the " Survival of the Fittest," but I am bound to confess that I do
not like the term, when thus applied.
If, at any rate, my views are sufficient to explain why many species still
remain common, we cannot deny that many others are rare ; and in facing the
problem of rarity, which we must now do, and in searching for its causes, it is
well perhaps to take the least important first and deal with the rest in an
ascending scale.
novitates zoologicae xxvii. 1920. 339
Climatic Conditions.
The weather must, of course, come in for its fair share of blame, but Para
would not be Para without it, and all things considered we enjoy a really wonderful
climate, the advantageous conditions which it produces being far in excess of its
drawbacks. (See General Conditions, p. 358.) My accusations, therefore, under this
head shall be limited to the following : Torrential downpours of rain, preceded
by sudden sharp gusts of wind of short duration, which undoubtedly dislodge
various larvae, and bring to their certain doom many that have only just emerged
from the egg ; floods, which must occasionally drown ill-located larvae and
subterranean pupae, but to what extent it is impossible to estimate ; excessive
humidity, which frequently, even in nature, produces fungoid growth to the
destruction of pupae with or without cocoons ; excess of direct sunshine, which
in certain localities burns pupae to death, or deprives larvae of pabulum by
drying up the food-plant. Such troubles, however, in Para do not amount to
more than, if as much as, they do in other parts of the world, nor do they apply
in any special measure to the Sphingidae. In fact, my experience inclines me
to the belief that even collectively they constitute the least of the destructive
forces which act and react upon the forms of life under consideration.
Predatory Foes.
A far greater responsibility undoubtedly rests with certain predatory foes,
which comprise a woefully long and varied list. To illustrate this, I can but
catalogue a number of individual instances which have come under my direct
observation, as follows :
(1) The " bemtivi " or golden tyrant, which is frequently seen assisting the
lamp-cleaner by consuming Hawk-moths as well as the smaller fry left from the
previous night. Not content with mouthfuls in moderation to be found in genera
like Epistor, Perigonia, and Sesia, he sometimes has the audacity to sample
with his damaging beak the large and showy representatives of Protambulyx,
Amplypterus, Oryba, and Pholus.
(2) The " bacurao " or night-jar, which carries on the same murderous
game at night, waiting silently on the ground just outside some illuminated
area in an open place, and rising to snatch the moths as they are drawn to the
light.
(3) Other insectivorous birds, small and great, and too numerous to mention,
of such families as Formicaridae and Dendrocolaptidae, whose life's occupation
is to hunt insect-eggs and caterpillars on leaf, stem, and trunk, and peck open
cocoons. Though I cannot here cite special instances, it can hardly be doubted
that young Sphingidae, especially when green, perish thus in considerable
numbers.
(4) Coming to domestic regions, the barn-yard fowl, the cat, and that par-
ticular type of pedestrian whose mind is as heavy as his boot, I rank in one class,
though they are not all birds. To their united and vandalistic efforts in the
immediate vicinity of dwellings must be ascribed a very considerable shortage
in those forms of living creatures which were surely meant to adorn the earth,
and which are just as harmless as they are beautiful. Ignoring the obvious
ravages of the hen and her brood, the chief victims are large Sphingid moths,
340 Novitates Zoolooicae XXVII. 1920.
" played " to death beneath every other street-lamp at night by cats, whose
more normal avocations in life are temporarily suspended. Then come the
great larvae of such genera as Cocytius, Protoparce, and Pachylia, which from
their size, movement, and vivid coloration on the dead earth or pavement
are very conspicuous objects, as they wander in search of suitable places to
pupate. The destructive instinct at once comes uppermost, and is unfortunately
not limited to children and school-boys. Though in many cases not in the
least like snakes, they are, of course, always taken for them, and must be squashed
or cut in half.
(5) Of insect-eating animals I cannot speak from personal knowledge, but
from the way in which small monkeys greedily devour cicadas, it is not un-
reasonable to assume that Sphingidae have foes even from this quarter.
(6) Then come the bats, whose ravages are but too well known. Though
Vampirus is mainly a fruit-eating genus, and others have a decided taste for human
and animal blood, the nightly destruction which prevails among the winged
creation in general, Sphingidae included, must be enormous beyond computation.
On favourable evenings in the main public square of Para, the central pavement
of which is adorned with a monument and four brilliant arc lamps, I have seen
as many as twenty very large bats at the same time, sweeping in and out of the
illuminated area, twittering vociferously in chorus and devouring everything
wholesale. I have many times seen one actually cling for a brief moment to the
wire hanging in proximity to the globe, gobble an cllo or two, disturb half a
dozen others with its wings, and decamp.
(7) Under the general head of reptiles, but especially lizards, the destruction
of Sphingidae, as of other families, is again enormous. The electric lamp is
once more the rendezvous for toads and frogs. There are huge olive-brown,
fat-bellied toads sitting beneath and ready to swallow up anything that is
unwary enough to alight on the ground, or being dizzy, and perhaps singed, falls
within the range of their leap. There are small frogs of several tree-climbing
varieties, which I have frequently seen not only clinging to the smooth iron of
the post, but on occasion quietly enjoying their suppers in line with forty or fifty
Hawk-moths upon the insulated wire leading to the globe.
Never, surely, was there such a place as Para for lizards in the matters
of size, abundance, and variety. They are to be found in every part of the
matto, wet or dry, in every garden, on every wall, and even in every house ; for
a small sand-coloured and semi-domesticated cousin, named " osga " (Hemi-
dactylus), is suffered to abide with us, because he is fond of mosquitos. " Osga "
also sits upside-down on enamelled lamp-reflectors at night and waits for moths.
I counted five the other day in passing a dozen street-lamps. But the point
to remember above all is that all lizards and snakes, so far as I am aware, eat
caterpillars and chrysalides, morning, noon, and night, and have apparently
solved the knotty problem most satisfactorily to themselves, that they of all
creation are the fittest to survive. The " acapu " palings which line the roads
and gardens of Para are largely tressed with creepers like Cissus, Echites,
Davilla, etc., and they are also thronged with lizards, untiring in their quest
for food. It is here that many heedless Hawk-moths of such genera as Pholus,
Epistor, Aleuron, and Leucorhampha deposit the greater portion of their ova ;
for it is here that I have periodically been successful in securing a first innings
at the egg-laying season.
Novitates Zoolooicae XXVII. 1920. 341
Assiduous and prolonged searching results in the discovery of many ova
and young larvae of these species on the out-branching tendrils and freshly-
expanding leaves, but not for long will you find them there. A number of
empty egg-shells and recently nibbled leaves too often betoken only that the
devourer has been devoured. A fortnight later you will be fortunate if you
discover a single caterpillar that had somehow escaped detection, and become
too tough and fat or too snake-like to be eaten ; for in such positions the waste
must be enormous, and it is clear that only the merest fraction of this potential
life can ever reach maturity. Considering the perpetual depredations of lizards
alone or in conjunction with other foes, the marvel is not that the majority of
butterflies and moths are scarce hereabouts, but that many species which are
rare survive at all. Possibly some have disappeared by this agency, and I
presume that we shall none of us ever be any the wiser. Possibly they represent
some of the missing links in that great chain of life of which to-day we behold
but remnants in certain isolated units which seem to hinge-on to nothing and
to defy classification.
(8) Next come predatory insects. I use the term freely for convenience,
to include all sorts of creeping, crawling, and flying creatures, which in turn
bite, sting, and devour lepidoptera in all stages of life. Prominent among these
are Arthropods such as centipedes and spiders, small and great, as well as lice,
beetles and cockroaches, locusts and Mantidae, wasps and other flies, and last,
but by no means least in effect, hordes of ants, whose ravages, whether conducted
singly or by universal onslaught according to the habit of the species, certainly
represent wholesale destruction on the grandest and most distressing scale.
For the scavengers of refuse we have nothing but approval, but Para is
so richly furnished that it has ants to eat everything, alive or dead, and half
one's time is wasted in the futile attempts at warding off their insistent attacks.
Besides the ants which fill your sugar-basin, eat your fruit, drown themselves
in your drinks, and invade your entire food-supply, there are ants to consume
not only your dried insects but living larvae and the young brood just out of
the egg, which have been carefully sleeved-out on some growing plant. The
sleeve-net is at once appropriated as the suitable locality for a new nest,
with the larder already stocked at close quarters.
On other occasions you import choice plants into your garden to serve in
larvae-rearing, and during the night they are denuded of every leaf by a train
of big red " saiiba " ants, whose earthworks may be in some one else's garden
a hundred yards or more away. A very large solitary black ant known as
" formiggo " (Ewponera) is often met with on the matto paths with a moribund
caterpillar between his jaws. In short, there is not a place, not a tree-trunk
nor a leafy bough, that is not the resort of one species or another of the ant
world. They literally swarm everywhere, and are responsible for immense
destruction.
The attack of a common black predatory wasp has recently been very
clearly demonstrated to me, still further explaining why the healthy young
caterpillar of yesterday is no longer to be found on his perch to-day. In an
attempt, which should otherwise have succeeded, to introduce a hardy species
of Citheronia, found commonly at Pernambuco but unknown here, I reared
some 300 young larvae from the egg. These were kept in the protection of my
bathroom until they had reached the second or third instar, and were an inch
342 Novitates Zoolooicae XXVII. 1920.
or more in length. Then, considering them tough enough to withstand the
elements, and sufficiently heavily spined to ward off predatory foes, I placed
them out in a large net open at one end upon a guava tree with profuse leaves
in my churchyard. Three days later my 300 were reduced to 3 by this miserable
black thief, several specimens of which were seen still exploring the boughs,
while one was actually inside the net munching at mangled remains. As no
further trace of the rest could be found, I presume that the majority had been
carried off to the nest.
Thus does the struggle for life continue, and I know of no place which offers
greater facilities than Para for the observation of its diverse phases and features.
Parasitic Foes.
We come now in order to the last but most insidious branch of foes to which
lepidoptera in their early stages are exposed — viz. Hymenopterous and Dipterous
parasites. Once again Para is full of them, and doubtless in many instances
they are in themselves undescribed species, or if they occur in collections, they
at any rate lack any demonstration of that intimate relationship with the various
species of lepidoptera on whose life's blood they were nourished in their own
larval stages. I have got nothing new in principle to narrate over and above
what is known to exist in Europe and other parts of the world, but only to record
the very widespread and pronounced character of this unlovely association in
Para, as evidenced by the large proportion of one's caterpillars, which to one's
disgust only produce flies and wasps. These may be very interesting in them-
selves, and I kill and label them off under the name of the host for future
identification ; but as it is impossible to specialize in all branches of entomology
at the same time, I will at once confess to being the victim of a relentless prejudice.
Among the Sphingidae, as illustrations of what I have too often experienced, I
may cite the following instances : The eggs, generally laid on the under-surface
of the tenderest leaves of the food-plant, are frequently " stung " by some almost
microscopic hymenopterous fly. After the lapse of but a few days there emerge
from one or several holes ten or a dozen of its progeny, which, marvellous to
relate, have completed their entire metamorphic cycle within the confines of
the egg-shell of the moth.
This I observed in Cambridge and Windermere years ago in the case of the
common Emperor-moth's eggs, and I have very frequently noted it not only in
connection with the large ova of Cocytius, Protoparce, Protambulyx, Pachylia,
Leucorhampha, and Pholus, but even with the smaller eggs of Xylophones, and no
species seems to be immune.
In P. syces, L. ornatus, and X. chiron, guianensis, anubus, and especially
mossi, the larvae are too frequently stung by dipt era, producing from 10 to 30
maggots with imagines resembling blue-bottles or the common house-fly. Many
are subjected to attack by both diptera and hymenoptera ; the larva of X. anubus,
for example, once producing a single and very large wasp grub which spun a
tough black silk cocoon.
The genus Protoparce is similarly troubled, not only by Diptera (the eggs of
the parasite in this case being generally introduced in the region of the spiracles),
but also, though more rarely, by a small wasp. In this latter case the full-grown
grubs of the parasite emerge through the back and sides of the still-living but
NOVITATES ZOOLOQICAB XXVII. 1920. 343
sadly attenuated host, and spin little yellow or white silken cocoons in situ,
standing up on end and reminding one of the almonds which sometimes adorn
a plum-pudding. The larvae of a small Hawk-moth in Pernambuco, Neogene
dynaeus, is thus literally decimated. On corresponding lines the genus Pachylia,
especially syces, which is so much rarer in Para than ficus, is stung by a very
small hymenopterous parasite, resulting in the production of some hundreds of
tiny flies from the body of a single caterpillar. In this instance, the larva, while
still clinging to a leaf, becomes completely encircled by a mass of tiny white
cocoons closely woven together. The writhing larva then falls out or is devoured
by ants, and what is left appears to be a thick lump of cotton-wool sticking to
the leaf, of tubular formation and open at each end.
In the case of dipterous parasites which affect species belonging to
Acherontiinae, Sesiinae, and Choerocampinae, and possibly the two other sub-
families, the exodus of the maggots from the body of the caterpillar invariably
takes place in the puparium, and even after the spinning of a slight but deficient
amount of silk. These Diptera, though bearing a striking resemblance to ordinary
flies, of course represent many distinct species. It is more than possible, however,
that some of the common parasitic species are by no means restricted to any one
kind of caterpillar, but thrive at the expense of the lives of a number of larvae
belonging to different species and genera or even to different groups. In other
families of Lepidoptera, such as the Saturn iidae, the larvae manage to pupate in
stout, well-woven cocoons with all the appearance of health, and only later do
the dipterous maggots break through the walls of the chrysalis within, and form
their own glossy brown oval cocoons alongside the corpse of their victim.
This sometimes takes place here with a few Sphingidae which spin a covering
web interwoven with fragments in the crevice of a tree-trunk, such as Isognathus
scyron. In other cases the metamorphosis of a species of Diptera, sometimes
that of one large hymenopterous fly, sometimes that of a number of small ones,
is completed within the confines of the pupa-case itself, from which the flies
emerge by separate holes.
This is frequently observed here, as elsewhere, as a pronounced feature with
many species of lepidoptera, the first prevailing with the Saturniid genus
Rothschildia. The last-named variety is especially marked in such species as
Papilio thoas and androgens, Aganisthos odius, Brassolis sophorae, Opsiphanes,
etc., among the butterflies ; and I have only recently discovered that Isognathus
allamandae Clark in Pernambuco is similarly attacked, though up to the
present I do not remember to have bred any Sphingid parasite of this particular
kind in Para.
For the sake of completeness, as being a prevalent form, one other type of
dipterous parasite deserves special mention. How far it attacks Sphingid larvae
I cannot say, but the large Nymphalids of such genera as Caligo, Catoplebia,
Opsiphanes, Dynastor, and Prepona are very extensively troubled by it. The
method of egg-laying on the part of the female parasite, which I have caught
in the act of ovipositing, is different, and for a brief period one degree less
damaging, in that it gives the caterpillar, or rather its captor, a fighting chance.
This I have repeatedly proved after a painstaking operation with the forceps,
in which the temper of the " stung " caterpillar is sorely tried. The eggs, which
are ochreous and tough, are gummed on. externally with diabolical accuracy of
instinct, sticking like ticks at one end immediately behind the horned head of
344 NOVTTATES ZOOLOOICAE XXVII. 1920.
the larva and in the interstices of the segments, so that the poor victim cannot
bite them off. If found before the young maggots have hatched and eaten
their way into the host's body, they may with great patience and care be
removed, one at a time, 10 to 50 of them, and the larva will pupate and
emerge as perfectly as if it had never been scented-out by so unwelcome a
visitor. This method of procedure is adopted by certain species of Diptera
in England, and I have more than once found the noble1 larva of Oryba kadeni
thus molested.
Such, then, are the forces of decimation among the butterflies and moths
of Para, and with parasitism in insect life I close my mournful list. The word,
from being originally applied to the drone in human society, has come now to be
used somewhat loosely, thereby losing some of its original force. In a true
sense the cuckoo, which has ceased to build a nest and rear its own progeny,
is a parasite. My use of the term here, however, is strictly limited to what
I consider to be degenerate forms of life, whose evolution has had a downward
tendency, and has involved the loss of an erstwhile independence by an unorthodox
dependence for nutriment upon the living and prepared juices of another species
in the same general order of creation. Such is our mistletoe, which no longer
needs roots, but sucks the prepared sap of the apple-tree and the oak, and survives
at their expense. Such is the Brazilian mistletoe, clustering as a thick yellowish
mass among the upper branches of Genipa americana ; such also is the " herva
de passarinho," which diminishes the health and fecundity, if it does not curtail
the growth, of the orange and mango, and others like the " abacate," among
the more indigenous trees of Brazil. Such, however, is not the orchid, which,
like many another plant (ferns, Bromeliaceae, etc.), only finds a lodgment and
support upon the trunk or branches of a tree, does not derive nourishment from
its sap, and is quite erroneously termed " parasita " in the Portuguese tongue.
Of parasitism among the insects I have already said enough to make my
meaning clear. That it has its uses in preserving the balance of nature by
limiting the over-rapid increase of those species attacked cannot be doubted.
It is a selfish and harassed world in which we live, and just as parasitism looms
large as a universal feature, so are we bound to acknowledge that this trouble
in the insect world is quite in order. My contention therefore is, not that it is
right, but that, so far as the present age is concerned, it is in full accord and
harmony with those laws which we find actively at work in every other department
of life. I contend, on the other hand, that it is very far from ideal, and that
by no stretch of casuistry can it be reconciled with the assertion made in Genesis
(chap. i. ver. 31), that " God looked upon everything that He had made, and behold
it was very good." No matter how allegorical such passages as these may be,
no matter how deficient as scientific statements, they stand, in my humble
estimation, in their broad general outlines for essential truth. And, though it
may be thought fanciful, I fail to understand how persons who refuse credence
to the second great dogma, known as " the Fall," can effect any sort of recon-
ciliation between nature and revelation. Accept " the Fall," and parasitism
at once becomes at least intelligible as a part, not of a fair creation, but of a
disorganized and perverted system ; and at the same moment, in the marvels
of the Divine economy, one of the means necessarily resorted to to prevent
matters from becoming worse.
Not therefore by adopting the so-called " scientific " view of former days,
Novitates Zoologicae XXVII. 1920. 345
not by ignoring the theological tenet regarding a fallen state, which for
too long has been deemed at variance with the theory of evolution, but by
accepting both the statements of the Bible and the plain truths of nature
can one read Darwin and Wallace, and may I add Huxley, with the immense
pleasure and profit to be derived from almost every page of their writings.
And, further, I claim that one can emerge from this fiery ordeal not a rationalist,
still less an atheist, but a believer still and a fuller believer, whose creed, if
it has been subjected to the rationalizing process, has only been shorn of
immaturity and excess, and readjusted to an altered perspective.
By way of forestalling a possible criticism, it is obvious, from the previous
verse to that referred to in the first chapter of Genesis, that vegetation was
meant to serve as food for animal life and creeping things, and it is equally
obvious that man was meant to eat animals ; but all this is the direct opposite"
of parasitism, taken as I understand the word.
To summarize, then, I cannot conceive it as any part of a very good creation,
though evolutionary changes subsequent to " the Fall " may have necessitated
it, that, for example, a healthily-nourished caterpillar, which has in itself all
the potentialities of becoming that for which it was intended, viz. a perfect
butterfly or moth, should have its vitals consumed by another creeping thing,
the larva of another insect, in fact, simply to complete its own metamorphosis,
no matter how equally perfect that other insect may be in the marvels of its
own construction. Is not the world large enough for all ? Its near relatives
still live on fruit or decaying wood or excrement, and at the least hasten on the
purifying process whereby these substances are returned to their primal and
scentless elements.
The degenerate parasite, on the other hand, slowly tortures another living
creature to death, and, having deprived the earth of an item of beauty so far
in excess of its, own achievements, leaves behind a putrid and stinking mass
for others to clear away.
However much truth the term " Survival of the Fittest " may cover, it
does so effectually cover up everything under that vaguely comprehensive and
indefinable word " fittest," that it seems but to shelve difficulties. What is the
fittest to survive, and why ? From what initial standpoint of enlightenment
and authority do we argue that any one living organism is more fit to survive
than another ?
Is it not from all the evidence before our eyes, those plain broad facts which
none can dispute or deny, that feeling bound to acquiesce in the inevitable we
give it a name ? My objection is solely ranged against the word " fittest," for
it seems to beg the question and to land us into an awkward dilemma. We all,
for example, have our sense of beauty as opposed to ugliness, and there is
even a general consensus of agreement upon the point. We all form relative
estimates upon the practical utility and worth of things throughout the entire
creation, animate and inanimate, and again there is a large general consensus
of opinion. But how does nature deal with beauty and utility ? She is stern,
relentless, and without discrimination, making no account whatever of our
conventional standards and values. As often, in obedience to those elementary
laws which enjoy universal sway, do her blind forces of destruction demolish
the beautiful and useful as they burn rubbish. As often, in her milder moods,
does she tenderly nurture the worthless weed by those same benign influences
346 NOVITATES ZOOLOGICAE XXVII. 1920.
with which she fosters some type of growth that we account precious. We are
left, then, to face two alternatives : ( 1 ) that our standards of appreciation and
valuation, no matter how world-wide their support, are all wrong, which I do
not believe ; for though confessedly conventional, they must bear some, relation
to the absolute ; or (2) that, in the face of our ideas upon beauty and utility,
those which actually do survive in the struggle for existence are thereby proved,
ipso facto, to be the fittest to survive, which I no more believe. I am aware
that I am employing the term in a somewhat unusual and restricted way, and
it is in this sense only that I contend that the word " fittest " is made to do
too much duty. At one time it stands as the equivalent of " strongest " or
" cleverest," at another it simply represents superior brute force or the greatest
cunning, or at best the most prepared. But it is when we come to a consideration
of those disintegrating forces like parasitism among insects and plants that our
rebellion against the use of the term " Survival of the Fittest " reaches high-water
mark : for the successful parasite, though transcending the wisdom of a Solomon
in the accuracy of its aim and in the attainment of its object — namely, supremacy
in the struggle for life — does so by methods which are discredited and are
altogether out of harmony with what we understand as the principles of justice
and morality. Though it may serve a useful purpose in the general economy,
judging by human standards, we are bound to acknowledge that on such occasions
it is the fit which disappears and something worse, less valuable or less beautiful,
which survives.
Right or wrong, fit or unfit, parasitism is assuredly and immensely responsible
for the reduced number of many representatives of practically all the lepidopterous
families, and consequently for the reduction, almost to vanishing point, of
one of nature's loveliest ornaments.
Each of the five subfamilies into which the Sphingidae are now classified is
represented in Para and in the following proportion : Acherontiinae 16, Ambulicinae
6, Sesiinae 47, Philampelinae 9, and Choerocampiriae 12; and just as there
are many other species of a more or less restricted range of distribution in different
parts of the immense region drained by the Amazon and its tributaries, so possibly
are there even more species near the southern side of its mouth than the 90 or
so which I have had the good fortune to come across. Due allowance must
of course be made for this in any subsequent remarks dealing with the parallelism
or difference which obtains between the species considered.
I now have some observations to make in regard to the features, habits,
and peculiarities of the Para Sphingidae, which, when correlated, apart from
any intricate or anatomical questions, constitute a striking array of facts, and
go far in suggesting a true system of classification. Those with which I wish
to deal are five in number : (1) Form, design, and colour of larvae ; (2) Pecu-
liarities of their excrement ; (3) Method of pupation ; (4) Form, design, and
colour of pupae ; and (5) The association of species or even whole genera with
some particular Order of food-plant.
(1) Form, Design, and Colour of Larvae.
Here I would notice at the outset the general similarity of young Sphingid
larvae on emergence from the egg, suggesting the close alliance of each species,
NOVITATES ZOOLOGICAE XXVII. 1920. 347
be it small or great, and forming the whole into one compact and well-defined
family, irrespective of subfamily distinctions. The character to which I refer
more particularly is the uniformity of the tail on segment 12, which at that
stage is always a noticeable feature, of remarkable length, speedily changing
from light to dark in colour, and when examined under the lens found to be
rough in surface, frequently bi-lobed at the extremity, and surmounted by a
single bristle on each fork. It is in this particular, or rather in the extraordinary
variety of tail-formation, the partial or complete loss of this appendage in the
succeeding stages, that we behold such striking specific differences. Stage after
stage, as the skin is moulted and successive instars reached, does each species,
ever true to its kind, exhibit a new form of tail or horn or hump, different from
that which preceded it, different from that which is to follow, and in many
instances, especially in the fifth and final instar, essentially different in length,
thickness, quality, curve, and colour from even its next-of-kin in the same genus.
This is most noticeably the case in the genus Xylophones, and perhaps least
pronounced in Isognathus, where an exceptionally long whip-like black tail is
retained up to the period of pupation, and where the difference between the
various species in this one respect becomes more one of degree in length, roughness,
and the presence or absence of a white ring or two.
It is surely worthy of note, though I will leave it with those better versed
in the laws of evolution to draw conclusions, that Isognathus is practically the
only genus in Sphingidae, so far as I am aware, that retains the long, rough,
flexible tail of the baby caterpillar to the full end of the larval period. Curiously
a few deceptive Notodonts possess a very similar appendage. The kindred genera
in this same subfamily Sesiinae exhibit very strange diversity of form in the
tail, Erinnyis, the next-of-kin with almost identical pupa-form, being characterized
by an appurtenance which in alope is like a rounded tusk, in ello and oenotrus
like a swollen knob, and then a mere nipple-like point in the last stage. In
Oryba achemenides, but not kadeni, it is like a sickle in the fourth instar and
only a button or nipple in the final. In Enyo, Aleuron, Madoryx, and Leuco-
rhampha, on parallel lines, the tail resembles a curved knife-blade, followed as
before by the mere button. Hemeroplanes bears a rather stout grey and curved
horn, while Pachylia has a small sharp spike in syces and a thick, blunt, but very
diminutive hook in ficus. In Philampelinae the tail of Pholus anchemolus, after
being reduced to a fine and absurdly disproportionate black hair in the foregoing
instar, disappears altogether in the last.
Its relatives Peacus fasciatus and vitis evolve on the same lines, but
P. labruscae shows a new development, exchanging the flexible and curled pink
filament of the fourth instar for a hard glossy disk, capable of a rapid undulatory
movement. The Ambv.licinae, from my restricted acquaintance with their
larvae, and the Acherontiinae, where I am more at home, seem in the main to
possess what we are accustomed to regard as the normal horn, partaking more
or less of the dorsal coloration of the larva or inclining to black, blue, or pink,
stiff and stout in construction, though more slender in Ambulicinae, rather erect
in posture, incapable of free movement, straight or finely curved, and generally
bristling with small setiferous tubercles. Herse cingulata, Protoparce sexta and
albiplaga are, however, exceptions to the rule, and, though it be only a matter
of degree, exhibit strongly curved and rather smooth horns. In Choerocampinae
the variety is so great that I fail in any attempt at description. Suffice it then
34S Novitates Zoologicae XXVII. 1920.
to say by way of contrast, that Xylophones gnianensis possesses a broad, thick,
and perfectly straight blade-like horn, rough like a file on both upper and lower
edges, but smooth on the sides ; while X. mossi in its last instar retains but
the merest vestige of a down-turned tail upon the anal flap.
True to the principles enunciated by Darwin in The Origin of Species, it is
this strongly pronounced but variable feature, representing, as I suppose, the
tail or horn possessed by the ancestral Sphinx, and ante-dating the various later
evolutionary changes, such as have necessitated subfamily divisions, which has
shown the greatest amount of variability in structure throughout the entire
family.
Nothing short of enlarged photographic diagrams, showing the evolution
of the tail of each species during its five successive instars, species after species
6et side by side for comparison, could serve adequately to portray the extra-
ordinary degree to which this caudal appendage of the Sphingidae has varied.
Coming to the later stages of larval development, colour and design, apart
from their adoption as protective measures by resemblance to surrounding
objects, seem also frequently, though with a few strange exceptions, to suggest
a sequential progression, or at least a circular grouping of species. I refer in the
first place to the seven lateral oblique stripes, so characteristic of Sphingidae
throughout the world ; to their irregularity in Cocytius ; to the greater regularity
of the same in Protoparce, P. albiplaga forming an exception ; to the fixed and
constant deviation from the normal type, depending wholly upon the difference
of food-plant in Protambidyx strigilis and Sesia ceculus ; to the extension of the
seven to an eighth or even ninth stripe in species of Epistor, Sesia, etc. ; to an
entirely distinct design in Isognathus, Pseudosphinx, Leucorhampha, and the
later stages of Erinnyis ; to their transposition, pointing up towards the head
instead of the tail in Pholus and Pachylia, P. resumens forming a most remarkable
exception to this ; to their reduction to five in diminishing ratio in Pholus
anchemolus and vitis, to six in eacus and their increase to eight in fascialus ; and,
finally, to the partial reappearance of the customary seven stripes directed
tailwards, when visible at all, in Xylophanes.
The presence of a medio-dorsal stripe is again a characteristic attribute,
appearing strongly in Cocytius, in many of the genera of Sesiinae, in Philampclinae,
and to a partial extent in Choerocampinae, but seldom strongly marked in
Protoparce and usually absent.
Possibly a still more important and significant feature, specially characterizing
the entire subfamily Sesiinae, with or without the addition of the oblique side-
stripes, is to be found in the enclosure of the dorsal area by two lines adorning
the face and continued at a slightly divergent angle, which then run parallel
and unite somewhat more abruptly at the tail. This pattern is totally absent,
so far as I know, in Acherontiinae, Ambulicinae, and Philampelinae, but reappears
strongly in some species of Choerocampinae.
Mere colour counts for but little, I presume, in the matter of classification,
being so largely a question of adaptation, but even here there are features worthy
of note. Though one occasionally meets with exceptions where the adaptation
to surroundings is less perfect than in others, the rule of course holds good that
green caterpillars with light stripes are to be found by day among the leaves
which they so closely resemble in colour and design, and on which they feed,
chiefly at night. Various devices are resorted to for protection during the day
Novitates Zooloqicae XXVII. 1920. 349
by caterpillars which are not green, or better, when they cease to be green
after any particular moult. It is thus with the later stages of Erinnyis, and
more especially with Madoryx and Leucorhampha, the larvae reposing with two
or three pairs of claspers tucked up and unused, geometer-fashion, on branch
or trunk, where they are by no means easy to detect. It is thus particularly with
those species of Xylophones which, while young and green or coloured like the
stalk, are well adapted to stay in the neighbourhood of the fresh shoots on which
they are feeding. Indeed, a long journey at this stage woidd be not only uncalled-
for, but would entail fatigue and danger. Quite the reverse, however, is the
case when, by successive moultings, the caterpillar has grown larger and stronger
and become brown, maroon, or peat-coloured. Then almost invariably is it
only to be found, if searched for by day, on the darkest and shadiest part of
the trunk near the ground, or quite frequently, as in the case of X. guianensis,
at some distance from the tree, lying on the earth among dead leaves and sticks,
an extremely inconspicuous object. The habits of X. anubus, loelia, and tersa,
in association with their particular plants, are identical ; but X. porcus and
chiron, which remain green to the last, have no need to move and seem to be
aware of the fact, finding an umbrella of leaves sufficient protection from rain
and sun and from prying eyes.
On several occasions I have found X. tersa by way of variety retaining a green
coat to the end of its larval period, and then, as though it knew all about the
matter, it was perched-up on the top of a spray of Spermacoce in broad daylight,
apparently justified for once in ignoring the secretive habits of its kind.
Poor X. mossi, which is nearly always " stung," is exceptional in its habits,
and would appear to be in a dilemma on account of its bright colour. When
young it is reddish-maroon, and there is no doubt that it wonderfully simulates
the little tailed red sheaths of the newly-expanding leaves of Pagamea, where
it rests and feeds. Sometimes it develops into a grey-green with growth, and
it is then equally well situated by remaining among the leaves. Usually,
however, the colour turns to a brilliant burnt sienna on the sides with a pink
back, lemon-yellow bands on segments 11 and 12, and five (sometimes six)
patches of viridian green marking the side-stripes. In this predicament, allowing
for the fact that the stems and branches of Pagamea guianensis are of a bright
sienna colour also, instead of seeking the shade it elects to stay, but is thus too
easily detected if at all exposed to view.
In the case of the highly ornate larvae of Pseudosphinx and Isognathus,
there is generally no attempt at concealment beyond selecting the under-surface
of a Plumiera leaf for shade, and sometimes frequenting the trunk or branches
in the blazing sun. As the well-known arrangement of warning colours largely
enters into their composition, alternating belts of black and white, or black with
yellow stripes and red heads, touches of blue or mauve, etc., I presume that they
are not wanted, and they certainly behave as though they were aware of the fact.
In this immediate connection it is interesting to note, the exception incidentally
proving the rule, that there are at least two members of the group which act
differently in this respect, Isognathus scyron and allamandae. These larvae are of
a grey-brown colour and distinctly dowdy by comparison with their more gaily-
attired congeners, invariably hiding away in perfect concealment during the day
on the dull branches or among the roots of Allamanda cathartica. They are not
Plumiera feeders like the rest, and it is significant that they should be almost
23
350 Novitates Zoologicae XXVII. 1920.
the only species of the group which I have noted as being occasionally stung
by both dipterous and hymenopterous parasites.
The mimicry of small snakes, if one is right in using the term, is a marvel-
lously pronounced feature in some species, and is to be had to perfection in
certain members of the Sesiinae subfamily, such as Madoryx and Leucorhampha,
in Pholus labruscae as an exceptional development in Philampelinae, and again
very specially in many species of Choerocampinae. As, however, this resem-
blance is effected by slightly, or extremely, different methods in almost every
case, I prefer to reserve the subject to individual treatment in connection with
the species thus enhanced.
(2) Peculiarities of their Excrement.
The next point upon which I wish to touch is the peculiarity of the excrement
or frass of Sphingid larvae, which though constructed, as I suppose, upon a
fundamentally uniform plan, and very similar to that produced by Notodonts,
Saturniids, etc., is strikingly different in distinct species, and very often acts
not only as a guide to the whereabouts of a larva, but informs the practised
collector in advance of its precise identity as a species. By this I do not mean
to infer that every single species can thus be discriminated in advance, but
that by previous acquaintance with the larva, its habits and its association
with some particular form of plant-life, the colour, size, shape, and general
character of the excrement will, in the majority of instances, if carefully observed,
betray the genus and very likely the exact species.
I know too little of the digestive organs of larvae to say exactly what takes
place, but the model upon which the excrement is constructed, a pellet of
hexagonal and tripartite form with a central core, is well illustrated by that
which is produced by Cocytius in the final instar. At this stage, in antaeus and
cluentius at least, it invariably breaks up at the moment of extrusion into 21
small brown fragments. In duponchel the pellet more often falls to the ground
whole, but being of a dry character, and the divisions being well marked, it
very readily breaks up as before into 21 pieces.
For brevity I must confine my remarks to the last larval instar. In Herse
the excrement is of an opposite character, being blue-black in colour, soft and
wet, and consequently so far welded into one piece as largely to obscure the
hexagonal design. This is even more the case in the genus Xylophanes, where
many species deposit stiff black or dark brown pellets of enormous and seemingly
impossible dimensions, and where the minute leaf-fragments are welded most
compactly, layer upon layer in rough oval formation, showing but a trace, if
anything, of the hexagonal design and nothing at all of the tripartite divisions
or the core. It is no exaggeration to say that in the cases of X. guianensis,
anubus, and mossi, for example, these pellets frequently approach an inch in
length, and are proportionately thick. In these instances, though the larvae
grow with exceptional rapidity, mossi never exceeding five days in its final
instar and still fewer in each of the four previous stages, the number of pellets
rarely exceeds 6 or 8 in the 24 hours. Conversely with other species where the
excrement is small and neatly hexagonal, Sesia titan and fatbits, for example,
will drop 50 or 60 pellets in the same time. P. sexta is a good illustration of
this, being a hardy, voracious, and almost continuous feeder ; but of the
Novitates Zoolooicae XXVII. 1920. 351
excrement of Protoparce in general it may be said that it is moderate in amount,
well-proportioned to the size of the larva, fairly regular in form, and in colour
dark brown, yellow, or green, largely in accordance with the nature of the
particular plant upon which the caterpillar has been feeding. In Protambidyx
the excrement of strigilis and eurycles is small and light green, the hexagonal
form being subdivided and giving it an exceedingly regular appearance.
This character is shared by Oryba and to a limited extent by Pachylia,
in both of which cases the frass, though large, is not excessive for such big
larvae. In Oryba kadeni and achemenides the colour is light brown, and as
it does not readily grow mouldy it is wont to retain its form for months after
the larvae have pupated. Its position beneath bushes of Palicourea or
Ourouparia, as the case may be, coupled with its size and general formation,
leaves one in no doubt as to the identity of the species, even if, as too often
happens, one is too late to discover the whereabouts of the particular caterpillar.
The excrement of Erinnyis and Isognathus is rather small, that of Pseudo-
sphinx somewhat elongate, hard and black, with sharp angular projections
and frequently bent. Pholus produces very large soft pellets of a light or dark
green coloration with the hexagonal form obscured but not obliterated.
So much at any rate for a subordinate branch of the subject, which, if
not the most savoury, is by no means devoid of scientific interest and is well
worth the attention of the student of larval habits and early stages, as it so
often leads to new discoveries.
(3) Method of Pupation.
Turning to the different methods employed in the formation of puparia,
a few brief general remarks are all that are necessary. I notice in the first place
that digging at the roots of trees for pupae is not only extremely arduous work,
but that so far as Para is concerned it is next to useless, as the larvae of almost
all species wander some distance on the ground and can seldom be traced.
Many are subterranean, and, judging from their habits in captivity, do not
hesitate to burrow deep into the earth to form their puparia in a loam that is
sufficiently plastic to enable them to dispense with silk in the construction.
So far as my experience goes, the entire subfamilies Acherontiinae, Ambulicinae,
and Philarnpelinae behave in this way. In Choerocampinae the method is
different, the larvae of Xylophanes never really entering the earth, but pupating
at some distance from the food-plant on the surface of the soil, and being
simply protected by scraps of growing or dead vegetation spun together by a few
strands of strong glutinous silk to form a covering.
It is in the subfamily Sesiinae that we see the greatest divergence in the
method of pupation. All the species can, I imagine, produce silk, and some
actually do produce a considerable quantity to form their cocoons. In Oryba,
Epistor, Perigonia, and Sesia subterranean methods are adopted, and the quantity
of silk is negligible. In Pachylia, Erinnyis, Pseudosphinx, Leucorhampha, Enyo,
and Aleuron the species pupate in a loosely-spun cocoon formed on the surface
of the earth among dead leaves and the roots of grass, etc. ; while in Isognathus
and Madoryx, though it be but a matter of degree, a very considerable and
completely closed-up cocoon is spun, not infrequently in the crevice of a tree-
352 Novitates Zoolooicae XXVII. 1920.
trunk or on rotten wood, any particles of debris within reach being used, as we
should expect, to stiffen the web and render it inconspicuous.
(4) Form, Design, and Colour oj Pupae.
Referring to the pupae themselves, I can but once again go through the
list and indicate the standard types, showing the lines on which species or genera
vary from one another. In general, however, it is worthy of note that all the
subterranean pupae, be they black, red-brown, or light mahogany in colour,
are nearly uniform in tint and devoid of external ornament; whereas those
species which spin cocoons, and remain more or less exposed to the light, are
in most cases adorned with a freckled or linear arrangement of markings.
The exceptions to this are to be found in such genera as Pachylia and
Leucorhampha, where the pupae, though highly lustrous, are of a uniform light
or dark brown, and Madoryx, where they are of a dead black, relieved by bands
of ochre-yellow in the interstices of two or three segments.
In Acherontiinae all the pupae vary slightly between a dark vinous and
a yellowish brown, and are more or less glazed.
Besides the cremaster, already referred to as possessing highly important,
even if minute, specific characters, there is also throughout this entire subfamily
the free but immobile proboscis-sheath, providing further good differentiating
features between the species by the peculiarities of its lateral ridges and its
curve, as well as its length and thickness ; but I am bound to acknowledge
that this difference is exceedingly slight between some of the species of
Protoparce.
In Herse the sheath makes a double turn and is readily distinguished from
all others. In Gocytius it is various, being a single but stout and well-protruded
loop in antaeus and duponchel, while cluentius possesses a complete spiral like
a small clock-spring or Ionic volute, owing to its greater length. It has been
a surprise and regret to me that after so long a time in the district I have been
unable to trace the early stages of htcifer and the rarer species beelzebuth and
Amphimoea walkeri, and can therefore say nothing with certainty about their
larvae or pupae. A large dried pupa in the Tring Museum, possessing a big
single-loop proboscis-sheath, Dr. Jordan thinks can be referred to no other
species than A. walkeri, but the data are absent. With the afore-mentioned
genus Protoparce the sheath assumes a big bold curve in rustica and perplexa,
is ample but more slender in sexta, diffissa, hannibal, and mossi, shorter but
stouter in albiplaga and lichenea. In the genera Eury glottis, Hyloicus, and
Neogene, so far as my experience goes, though none are found in Para, this sheath
is simply a small turned-down piece lying in juxtaposition to the abdominal
cases, as in the common Privet and Pine Hawks of Europe.
The plain light brown chrysalis-form, more or less elegantly curved, without
free proboscis-sheath and differentiated by many slight variations — such as the
precise tone of colour and degree of glaze — is shared by many species in common
belonging to the three central subfamilies. Such features characterize Pro-
tambulyx, Pachylia, Oryba, and Pholus ; while Madoryx, Leucorhampha, Epistor,
Perigonia, Sesia, etc., approximate to one another in darker hues. On the
other hand, a certain standard pattern is adopted by Isognathus, Erinnyis,
Grammodia, Enyo, and Aleuron, where the ground-colour varies between a
Novitates Zooloqioae XXVII. 1920. 353
reddish yellow and a light straw yellow, and the entire surface, which is highly
glazed, is more or less heavily adorned with tar-black lines and spots.
In Xylophanes an absolutely distinct type prevails in an elegantly-shaped
but generally not very lustrous bone-coloured chrysalis, possessing a fine black
line down the front to delineate the proboscis-case, an interrupted rnedio-dorsal
line in black or brown, big black spots enclosing the spiracles which are of a
dull red, while the rest of the surface is freckled by light umber patches and
finely-pencilled lines and dots of a deeper hue.
We have already stated that the cremaster stands first and foremost as a
distinguishing character ; and as with the variations exhibited in the tails or
horns of the larvae, so here a complete enlarged diagrammatic representation
of the cremasters of all Sphingidae for comparison, group by group, is a decided
want, and would form an adjunct to the evolutionary study of the family of
the highest importance.
Speaking generally, however, for a moment, and by way of leading up to
the last phase of the subject with which I wish to deal, and which I trust will
be found by no means the least important or the least interesting, I must first
make reference to such items in my collection where I am still in the dark as
regards their early stages. Some few of these have occurred singly and rarely
as moths, and, providing no clue, have defied all my repeated attempts to
investigate their origins. A few others have only been taken once or twice in
the larval condition and subsequently bred. Some have been chance finds,
in the first instances at any rate, while others have only been found after diligent
and prolonged searching, and by testing to the fullest extent possible every
hint which the first discovery seemed to suggest in regard to food-plant and
locality.
This has involved an increasing acquaintance with the botany of the district,
and in this department I have at all times received most valuable information
from the enlightened authorities of our local Museum and Botanic Gardens.
I refer to Mr. F. Ducke, Miss Snethlage, and the late Dr. Huber, — a botanist of
world-renown, whose untimely death through appendicitis in 1913 was a
deplorable loss to the science, and whose skilled aid, in conjunction with that
of the afore-mentioned friends, has to me been invaluable as an introduction to
this vast study. The Flora Brasiliensis, an extensive series of volumes, but
still largely incomplete, especially as regards Para, has also at times been useful.
Finally, the authorities of the Botanical Department at South Kensington have
on several occasions, when consulted, been most kind in rendering expert advice
in the matter of identification.
To one and all I am greatly indebted. It has perhaps given us all some
extra work, but it has not been labour wasted, for by the mutual interchange
of thoughts, ideas, and information on any given subject related to one's own
particular study, knowledge has been disseminated, and our conceptions as
individuals in our own lines of research have been broadened and amplified.
Not infrequently also has the co-ordination of scientific facts in the realms of
botany and entomology, which in their interdependence run on marvellously
parallel lines, led to a happy readjustment of ideas that aforetime were hazy,
and to the correction of positive errors. Hardly less important has been the
marking of certain exact spots in the great border-line of knowledge which man
has not yet passed, but which with time and patience, " by mutual sympathy
354 NOVITATES ZOOLOGICAE XXVII. 1920.
and mutual aid," he assuredly can encompass. I refer, for example, to quite
a number of plants and insects which are still unknown to science, and conse-
quently as yet possess no specific names, though their genera may be obvious.
I refer also to a perfect host of lepidoptera, where some species are still waiting
for a name and an approximately correct family status, and where anything
like a full and complete system of classification, whatever else may count, must
comprise some elementary acquaintance with early stages. In Europe, where
so much has been done, and where the material is so meagre by comparison
with the tropics of America, we are apt to imagine that if only we go about the
matter in the right way, some one can surely be found who will be able to tell
us all about the butterflies and moths of the latter continent. Nothing could
be further from the truth ; and yet it was some such idea that I myself entertained
before I went out to Peru in 1907 and found that in this, as in other matters,
there was no high-road to knowledge, no pleasant hand-books of botany and.
entomology, and no collector's guide to the district. What one does find is
the wealth of Nature's resources which baffle description, coupled with an array
of unforeseen difficulties and drawbacks which equally thwart one in the
endeavour to wrest from her more than a mere tithe of her secrets. While
making due allowance for all the splendid scholarly works on insects in general,
and especially for those on particular groups and families, that have yet been
published, the fact remains that the early stages of very many species of
Lepidoptera, including some of the most beautiful forms in the natural creation,
some of the most curious, some of the most grotesque in their marvellous adapta-
tion to environment, are still, in the great majority of instances, unknown to
science.
If you have a collection of exotic Lepidoptera you may, by visiting one or
other of the standard collections of the world, experience but little difficulty
in getting most of your specimens named with a correct Latin designation as to
family, subfamily, genus, and species, and you may also learn much as to the
range of distribution which any particular species enjoys. But when it comes
to the question of early stages, with even the most willing and enlightened of
informants, there is often no one who can tell you in a thousand instances what
the caterpillar looked like, what it fed upon, whether there was anything beyond
the ordinary in its method of pupation or the egg-laying of its mother, or indeed
anything at all about its habits as a living organism. Herein to me lies the
intense interest of the quest, but when all this is unknown more than half the
interest of a collection of moths vanishes. Having collected now for more than
thirty years, with an ever-increasing enthusiasm as experience became enlarged,
I have come more and more to regard a big collection with feelings akin to dismay.
Though it be the outward and visible result of years of patient toil, in itself, and
apart from other considerations, it can impart such limited information about
that great world of life which lies behind it. The collection, without doubt, is
highly necessary and important as a library of reference, case after case is very
beautiful, a species here and there and now and again a whole genus exceptionally
so, while another set are dull and monotonously alike to the untrained eye.
But whether showy or plain, the fact looms larger than it once did that it is a
cemetery of corpses, more or less well-embalmed and preserved, and, if well-
ordered, possessing a number of interesting memorial tablets and epitaphs !
The mournfulness of the spectacle is of course considerably diminished and the
Novitates Zoolooicae XXVII. 1920. 355
interest sustained when whole families are entombed together under glass to
facilitate the study of the comparative anatomy of their mummied remains,
and especially when the epitaphs are generous enough to afford not only the
name but the birth-place and date of decease !
Lest, however, I should shock any orthodox mind by such profane sentiments,
let me at once call myself to order with an apology for my tangential wanderings
and for discoursing at such length, and let me proceed to give some of those
touches from the life, with which, at any rate, no one can quarrel, however
much he may deplore the limitation of such information as is now available.
(5) Sphingid Larvae and their Food-plants.
We come then, finally, to a phase of the subject which has long appeared
to me to be one of intense interest and importance — namely, Sphingid larvae
and their means of sustenance.
In a land that is nearly all forest, where the vegetation is rife and luxuriant,
where in hundreds of cases one tree bears the strongest outward resemblance
to another, but where, nevertheless, the range of absolutely distinct species in
particular localities is in reality so great as seemingly to equal the number of
individual items of plant life which greet the vision, it is not unnatural to inquire
how is one in such a labyrinth of green to find out the names of particular species.
How indeed, unless sooner or later one can come into touch with some very
experienced informant !
But in truth, the finding of a name, the necessary symbol of communication
though it be, is not the first point in order of importance. What I mean to
emphasize by saying this is the paramount importance of first adjusting the
eye to those nice shades of difference in plant-life which distinguish closely-allied
species, and, still more important, species not at all allied but belonging to different
Orders, and bearing often an extraordinary superficial resemblance to one
another. The bewildering tangle of growth which characterizes the Amazonian
forest not unnaturally tends to obscure its less prominent details ; and it is
only after weeks, perhaps months, of experience in the same locality, that one
is able to form some rough mental classification, and focus one's eyes upon
individual objects. Then with the observation-faculties intensified, one learns
by degrees to be less led by appearances, and to appraise at their true worth
those characteristics which are more fundamental and which bind together
in one great Natural Order many forms outwardly dissimilar.
The specially-favoured locality selected by different trees and plants also
calls for attention, be it the humidity and shade of overhanging matto-growth
with its rich soil of decayed vegetation, or the region specialized by tabatinga
clay or white sand, the sun-scorched dry and open " campo," the " capoeira "
or simple woodland, the " igapo " or forest swamp, or the land to a greater or
less extent under cultivation with its fruit-bearing trees, each special in itself,
and each with a varied and specialized flora and fauna attached. In fact, to
put the matter shortly, an abundance of quiet field-work with the closest
observation of almost everything is undoubtedly the first requisite. Then it
is time to secure a few names, if these have not already been obtained ; and
if the species, and perhaps the genus too, cannot readily be identified, one ia
seldom so out of luck's way as not to learn at least the Natural Order, which,
356 NOVITATES ZOOLOGIOAE XXVII. 1920.
as I shall endeavour to show, is often the most valuable of the three, and ought
always to be recorded when possible. On procuring some desirable caterpillar,
my plan is generally to take it home in a tin with a sufficient amount of its
special plant to serve as food, and also a good sample-specimen to dry and
preserve for future identification, not forgetting to note down its association
with that particular larva. One speedily learns that it is often not possible
thus to identify the plant without its flower, so this too should be sought for,
though it is sometimes tiring and disappointing work. Further discoveries
reveal the same larva, it may be, upon a number of distinct species which ultim-
ately prove to belong to the same Order, or to one in the same general group
of plants. The recognition of this alliance in the plant-world next offers a
clue which, if followed up, not infrequently leads to the discovery of an allied
caterpillar upon a kindred plant, and little by little one learns, for example,
that an entire lepidopterous genus is associated with some particular genus of
plants, or is at least confined to the group. Equally worthy of note is it that
allied genera in the same lepidopterous subfamily are in frequent instances
similarly restricted to one and the same Natural Order of plant-life. The last
point in this connection is no less striking — namely, that an occasional instance
occurs where an Order like Vitaceae, or possibly a single genus of that Order
like Cissus, or the common grape-vine itself, will serve as a pabulum for species
so distinct as to represent no fewer than three different subfamilies like Sesiinae,
Philampelinae, and Choerocampinae, though this of course is very exceptional.
The result of all these revelations has been to emphasize in my mind the great
importance of the Natural Order, to give it always in this connection the place
of precedence over generic or specific distinctions, and to work for the discovery
of the larvae of those species which still remain unknown largely upon the
analogous principle that they will probably some day be found to be associated
with some plant or plants closely akin to those already known as the food-plants
of kindred species in the lepidopterous world.
I will give three examples in application :
(1) Seeing that three species of Cocytius in nature feed on at least six species
of Anonaceae, and perhaps a great many more, it is highly probable that the
remaining two in Para, together with the closely-allied Amphimoea walkeri,
are also Anonaceous feeders. Up to the present, however, this species with
Cocytius lucifer and beelzebuth have only occurred as moths, and I have to confess
my inability to trace their larvae.
(2) In Para we have three species of Protambulyx and three of Amplypterus,
and the whole six appear to be closely allied to one another. By exploring the
caju tree, Anacardium occidentale, and the taperiba, Spondias lutea, and at least
three other wild species belonging to this same Order Anacardiaceae, I have
very often come across larvae sufficiently varied to convince me that I had
secured different species, and as often have I been doomed to disappointment
by breeding nothing but typical P. strigiiis. By continuing, however, to work
on this principle, I have at last succeeded in finding the larva of P. eurycles on
an Anacardiaceous tree like the ash, locally known as " tapiririca."
The moth is common enough to leave me still wondering why its larva does
not turn up more frequently, while as for P. goeldii and the genus Amplypterus
I am yet no further advanced.
(3) Out of 12 species of Xylophanes in Para I have taken the larvae of 7,
NOTITATEa Zoolooicab XXVII. 1920. 357
and, though two can feed on plants of distinct Orders, all but one in nature
have been found associated with Rubiaceae — such as Spermacoce, Palicourea,
Psychotria, etc. There is, therefore, a fair presumption at least that all the
remainder are Rubiaceous feeders, and that in proportion as the alliance between
any two or more is close, so are their larvae likely to be found feeding on these
same plants or on species close akin.
Perhaps the most striking exception to the general rule is to be found in
Protoparce, which as a genus is commonly associated with Solanaceae, but where
albiplaga seems to be limited to Boraginaceae and Anonaceae, the latter seeming
to suggest a connection with Cocytius, which is extremely interesting. P.
lichenea I have only taken on Citharexylutn, a Verbenaceous plant, while the
common rustica associates itself with many plants in Verbenaceae, Boraginaceae,
Bignoniaceae, and Oleaceae, but never with Solanaceae. Among the remainder
of my acquaintance P. sexta, hannibal, and the rare perplexa are occasionally
seen to be sustained in nature by two or three species of Aegiphila, another
Verbenaceous genus, in place of their more customary Solanaceous plants. In
the Andes of Peru I found the larvae of Euryglottis davidianus associated with
Boraginaceae and Bignoniaceae, and as Euryglottis comes next in order to
Protoparce it is highly instructive, providing a wealth of suggestion to the
explorer, to learn that botanists group Boraginaceae, Bignoniaceae, Verbenaceae,
and Solanaceae together in the series Bicarpellatae of the Gamopetalae. So
once again our exception hardly does more than prove the rule. One is naturally
led to suppose that there are important ingredients in the chemical composition
of the leaf which are shared alike by all these plants, though so seemingly diverse
in form, and that this nutritious principle is essential to the life not only of
Protoparce, but of other species of other genera in Acherontiinae.
Here, surely, is the evidence of design, to be accounted for as Darwin did
by some grand evolutionary modifications in both plant and insect, running
on parallel lines and reaching back into the remote ages of the past. Coming
to present times, however, and allowing for the exceptions which greatly increase
the number of those Natural Orders selected to provide food for Sphingid larvae,
it is a striking and significant fact, and one which came to me as a revelation of
analysis, that of the 63 Para Sphingidae whose early stages have been revealed,
leaving at least another 27 where they have not, no fewer than 17 are associated
in nature with Apocynaceae, 14 with Rubiaceae, 8 with Vitaceae, 7 with the
gamopetalous Bicarpellatae, and the remainder as follows : Dilleniaceae 4,
Anonaceae 4, Moraceae 3, Onagraceae, Euphorbiaceae, Papayaceae, Anacardiaceae,
and Asclepiadaceae 2 each ; Convolvulaceae, Piperaceae, Sapotaceae, Polygonaceae,
Melastornaceae, Loganiaceae, and Vochysiaceae 1 each.
Though I have occasion to refer to several other species of Sphingidae
beyond the above 90, I naturally exclude them from my Para statistics. They
form, as it were, a supplement, too small to stand by themselves, and too in-
teresting to be ignored simply because they happened to live, one of them at
Pernambuco, one in the Antilles, one at Iquitos, and three others anywhere
from 500 to 1,000 miles up the Amazon.
In conclusion I may say that, with the Sphingidae as one of my keenest
specialities for a long period, I have striven to gather together every scrap of
possible information relating to the life-histories of such species as have come
under my notice. With this then, for the present, I must ask my readers to
358 Novitates Zoolooicae XXVII. 1920.
be content, and wait in hope for that day when errors shall be corrected and
a few more gaps filled.
Paha, January 1919.
GENERAL CONDITIONS.
Under this heading I have briefly sketched a number of more or less dis-
jointed facts and figures, which may enable the reader more readily to picture
Para and appreciate its advantages and disadvantages as an entomological
centre. Such notes are often of considerable use to the practical collector.
Belem (Para), with a population of about 120,000, is the capital of Para,
the third largest State in Brazil, and is situated 1° 27' south latitude by
48° 30' west longitude.
Though nominally at the mouth of the Amazon, a glance at a large-scale
map will show that the main bulk of Amazon water reaches the sea north of
the great delta island of Marajo, whereas Para stands near the confluence of a
distinct river-system, the immense Rio Tocantins proceeding from South Brazil,
the Moju, the Acara, the Capim, the Guama, and the Guajara. All these rivers
are tidal and, with the exception of the Tocantins, very muddy, the rise and fall
being 8 feet for neap tides and over 12 for spring tides. The general elevation
above sea-level is only a few feet, the highest part of the city being about
40 feet.
Pictorial Aspect. — Faced on west and south by Ilha das Oncas and innumer-
able other islands, which partake of much the same character as the swampy
part of the mainland. Backed closely on other sides by unlimited matto, an
impenetrable jungle of virgin forest growth. Immediate south-east and east
largely igapo or swamp region, practically impassable, even in the paths cut
by seringueiros (rubber gatherers), after heavy rain or high tides. Railway
cuttings through the matto run north to Pinheiro, passing through a tract of
very white sand with a modified vegetation at kilometre 11, and in a north-
easterly direction to Braganca. Roads leading from the city among the palm-
thatched and humble dwellings of the caboclos (people of more or less Indian
origin), towards the rivers or the forest, are known as travessas. These include
many small fruit-gardens which generally abut on second-growth forest. Most
of the travessas are broad, are cut at regular intervals, and are intersected by
others on the rectangular block principle. They are the streets of a larger city
in the making, but are still covered with grass and weeds like Spermacoce, etc.,
some being used for pasturage, and parts of some being distinctly swampy.
The forest is divided by a network of igarapes (small tributary streams), the
majority being muddy and subject to the rise and fall of tide, while a few are
peat-coloured and clear with sandy bottoms, owing to a slightly increased
elevation.
Unlike the Isle of Marajo, which possesses broad, open campos for cattle-
grazing, our open spaces are very limited in number and extent, and are probably
all of artificial origin. The " Bosque," situated outside the city at Marco
da Legua, is a decent tract of original matto or forest, about 500 metres
square, intersected by shaded paths and adorned with fountains and shelters
as a resort for the public. Its conservation represents a degree of good taste and
foresight which is somewhat exceptional in this part of the world. The Morphos
NOVITATES ZOOLOGICAE XXVII. 1920.
359
and other woodland butterflies are often to be seen here, and not infrequently
have I here procured some larva of worth upon the undergrowth, or detected
the presence of others altogether beyond my reach in the highest trees by their
excrement scattered over the sandy paths. The public prafas, squares, and
gardens of the place are characterized by many trees imported from other
countries, chief amongst which may be mentioned the Mango and Ficus benjamina
as shade-trees in the streets, the banana in all its forms, and a number of oranges
and lemons. These, coupled with certain flowering plants, garden palms, and
other importations like Artocarpus, the " Jaca " and the bread-fruit tree, etc.,
naturally tend to produce in the mind of the visitor a completely erroneous
impression in regard to the really indigenous flora of this part of Brazil.
Owing to the kindness of Miss Dr. Snethlage and of Sr. Rudolpho Siqueira
Rodrigues of the Museu Goeldi, I am enabled to give some interesting statistics
in regard to the climatic conditions of Para for the past eight years, 1911 to 1918
inclusive.
Bainfall.
Temperature (Centigrade).
Hygrometer
(per cent.).
Millimetres.
Days of rain.
Maximum.
Minimum.
Medium.
1911
88
2,550-2
272
33-6
21-4
25-4
1912
86
2,918-3
323
33-4
21-9
25-3
1913
88
2,616-8
280
33-6
21-6
25-5
1914
88
2,299-6
252
34-6
21-4
25-6
1915
89
2,042-3
215
34-6
21-7
26-3
1916
89
2,638-4
218
32-9
221
25-6
1917
89
2,809-7
248
320
220
25-8
1918
89
2,541-6
238
21-4 =
26- 1 =
Fahren
heit 90-7
70-5
790
The above figures indicate that in relation to its proximity to the equator,
Para possesses a remarkably high degree of atmospheric humidity, frequently
reaching' a state of absolute saturation, and as a direct consequence an excep-
tionally moderate and uniform temperature. This is roughly 80° Farenheit
in the shade of one's living-apartments throughout the year. The wet season
normally begins during the second half of December and ends with May. The
hottest month is nearly always November, the wettest February or March,
and the coolest period from July to October inclusive. In 1916 and 1917,
however, July was an exceptionally hot month, as was the close of August in
1918. The wet season is accompanied by much thunder and lightning and by
many very heavy, but only occasionally prolonged, falls of rain. It is to be
noted that even during the dry season there is seldom a week or ten days without
any rain, but that then the rains are more regular to time of day and of short
duration. The result is perennial green and a vegetation which seldom hangs
limp.
Though times have changed considerably since the days when Dr. Alfred
Russel Wallace and Mr. Bates spent their six months in Para, living near the
village church of Nazareth in a wooden hut at the delightful price of 30 milreis
a month, and though the population has probably trebled since then, there are
still a few ancient landmarks. The Nazareth Praca, for example, is still there,
360 Novitates Zoolooicae XXVII. 1920.
but is now, of course, a definite part of the city, surrounded on all sides by houses.
The church of their day has long been replaced by a larger edifice, close to which
I myself lived for some months. This is still so popularly attended that it is
now giving way once again to a more spacious building of very greatly improved
solidity and architectural form. The famous Nazareth Festa, though degenerate
in its cheap-jack association and modern cinema shows, is still the great feature
of the place every year as October comes round ; we still drink purple " assahy "
with or without " farinha " ; and still, most assuredly to an increased extent,
have our nerves shattered by innumerable rockets, fired off at the slightest
pretext at all hours of day and night. The old city of Belem, with its fine
cathedral and castello, can have changed but little in outward appearance since
1848 ; but though the chief markets are still at Veropeso, the centre of the
city, territorially speaking, is to-day marked by the Largo da Polvora, the Theatro,
Cafe da Paz, and Grand Hotel, the last two providing excellent accommodation
for visitors. Close to this, and leading towards the beautiful Largo de Baptista
Campos, in former days all wild matto, is the ancient British cemetery, dating
from 1815, where, through the generosity of English banks, business houses,
and especially Messrs. Booth & Co., I was enabled in 1912 to build a small English
church. The old mud-stretches of the Para river fronting the city have now,
with the exception of the Veropeso dock, all been mercifully buried beneath many
thousand tons of clean sand, a factor which has contributed largely, not only to
the appearance, but to the health of the place, not one case of yellow fever, so far
as I am aware, having originated here since the early months of 1911.
A bad name dies hard, and at this late date it is really surprising to find so
many persons of education who know nothing of Para's charms, and who merely
regard it as a mud-stretch and a death-trap to the white man. Though hot and
lacking the salt sea-breezes of towns on the coast, there is probably no pleasanter
or more comfortable place in the north of Brazil than Para, none so up-to-date,
and none that is freer of fevers and epidemics. As in other parts, there is, of
course, the ever-present malaria of the tropics, but it constitutes no serious
menace to Europeans passing through or settled in the city. Camping out in
the forest without a mosquito-net is of course to be avoided ; but with some
such preventitive, which is always a comfort whether in town or country, there
is really nothing to be feared.
The rickety wooden trapiches or piers of former days have now been replaced
by a stout wharf of concrete, upon which stand a number of great corrugated-
iron sheds. Alongside these lie tethered not only river boats but ocean liners
with a draught of 20 feet or more, which continue their journey for a thousand
miles up-river to Manaos. Boats drawing from 16 to 18 feet of water proceed
to Iquitos in Peru, no less than 2,200 miles from the Atlantic, so immense in
breadth and depth, as well as in length, is this South American Mediterranean.
Finally, Para is to-day magnificently served throughout by an adequate
supply of speedy electric cars, called " bonds," not to mention the ubiquitous
automobile, 300 of them at least; and the well-built houses and well-paved
streets, which in the main are distinctly above the South American average,
are brilliantly illuminated by electricity.
Novitates Zooloqioae XXVII. 1920. 361
NOTES ON THE SPECIES.
Having already dealt at considerable length with so many general questions
touching not only the characteristics of genera but the individuality of species,
repetition would be superfluous ; and as some of these species are common and
well known, my notes on them can well afford to be brief and scrappy, and
must be regarded as merely supplementary to what has gone before. The
Detail Index, which comes later, provides, so far as I have found it possible,
the full list of local food-plants with their localized popular names, if any ; but
I have refrained, as inconsistent with the title of the present work, from intro-
ducing the names of those particular plants which serve the species in regions
remote, but which either do not grow in Para, or are seldom, if ever, selected
as the natural food-supply in this part of the world.
For descriptions of the moths, their general range of distribution, as also
their subspecific or geographical differences, matters which do not come within
the scope of my treatise, I must in all cases refer my readers to the work by
Lord Rothschild and Dr. Jordan, entitled " A Revision of the Lepidopterous
Family Sphingidae," issued as a Supplement to Vol. IX. of the Novitates
Zoologicae of Tring, England, in 1903. The species are here numbered
according to the Catalogue.
T.Z.8. is an abbreviation for Transactions of Zoological Society, London,
vol. xx. pt. 2, and refers to Plates in Sphingidae of Peru.
N.B. — Larvae are described throughout as possessing 13 segments, the
head, for uniformity's sake, counting as No. 1, the leg or thoracic segments
being Nos. 2, 3, and 4, the post-thoracic segments 5 and 6, the clasper segments
7, 8, 9, and 10, the tail or horn being situated on the back of 12, and the anal
flap and claspers constituting segment 13.
Subfamily ACHERONTIINAE .
4. Herse cingulata. (Plates T.Z.S.)
R. & J. p. 10.
Larva secretive in habits and seldom met with except by systematic searching.
In colour, markings, and form up to fourth moult resembles Protoparce with a
straight horn. In final stage very different, possessing curved horn and usually
more brown than green, but widely variable. Moth common at light in Para,
but I have not observed it at flowers like II. convolvuli in Europe.
33. Cocytius cluentius. (Plates 1 & 2.)
R. & J. p. 54.
A common species in Para, the moth in both sexes often appearing at electric
arc lamps. Larva twice found feeding on Piper aduncum, a seemingly strange
departure from the customary Anonaceae, Biribd, Oraviola, Araticu, etc. ; a
somewhat pronounced aromatic odour being the only apparent feature in common
between the two Orders.
Young larva dull sage-green and white, side-strijies irregular in length and
362 NOVITATES ZOOLOGICAE XXVII. 1920.
breadth, and merging into the medio-dorsal band in a series of Vs. Fourth
instar with fine, light, and scattered hairs, and minute yellow tubercles on
thoracic segments, especially segment 2. A couple of broad and composite
bands, which are conspicuous by their nebulous whiteness and great length,
spring from the base of the post-thoracic segments, with three others in rapidly
diminishing ratio in front, and all merge in narrow V-formation into the white
medio-dorsal line. Three others, very faintly indicated on a deep green ground,
represent the customary fourth, fifth, and sixth side-stripes, while the seventh
leading up to the horn is once more marked by a nebulous white band which
stands out conspicuously, but melts away into a bluish ground. Horn emerald
and glazed with small yellow setiferous tubercles. Anal portion dull blue,
but flap brightly edged with yellow-green. In adult stage uniformly hairy like
antaeus, but always very white. Description in R. & J. correct but deficient.
Pupa, like all in Acherontiinae, subterranean and bright mahogany in colour.
The proboscis- sheath is so long that it makes as much as 2\ concentric turns
in the form of an Ionic volute.
Length of proboscis very variable : in female moth &\ to 10} in., in male
10} in.
34. Cocytius beelzebuth.
R. & J. p. 55.
My remarks below on the occurrence of C. lucifer and the uncertainty of
its appearance apply equally here, except that I can say even less of this rare
species, having only captured the moth at light in Para on three occasions, once
in 1911 and twice in 1912, a female on July 4 and a male on the following
day, both in perfect condition.
35. Cocytius duponchel. (Plate 1.)
R. & J. p. 56.
Undoubtedly the commonest species of the genus in Para, both sexes
occurring freely at light. Larva without any of the short hair which forms such
a pronounced feature in cluentius and antaeus. Side-stripes, except the third
and seventh which are white, but faintly delineated in all instars. Intensity
of colour, as with many green larvae, variable in individual specimens, and
generally well matched to the particular variety of food-plant selected. Markings
more intense when ground colour inclines to yellow-green, fainter when com-
pounded or combined with white-green. Proboscis-sheath of pupa, though
stout, well-curved, and much swollen at the extremity, is nevertheless distinctly
shorter than that of antaeus.
The male moth possesses a very strong, musty, and disagreeable odour,
akin to that of the cockroach. This is shared somewhat by other Sphingids and
by some Liniacodids, but generally to a less noticeable extent.
Length of proboscis in female moth 3 J in., in male 3} in.
36. Cocytius antaeus medor. (Plates T.Z.8.)
R. & J. p. 57.
Moth in both sexes common at light in Para. Food-plants, as in the last
species, exclusively Anonaceae. Rounded head of young larva becomes extremely
NOVITATE3 Zoolooicae XXVII. 1920. 363
arched or pointed on the crown, as in Protambulyx, but recovers some rotundity
in the final instar.
In all stages, and in the three species with which I am acquainted, the
larvae are wont to repose geometer-wise, the forepart hanging free from stem
or leaf, with two or even three pairs of claspers tucked up and unused. When
disturbed it wags itself violently and repeatedly from side to side, another
character which it shares to a pronounced degree with Protambulyx. Different
to those found in Lima, Peru, the full-grown larva here, as in Manaos and Per-
nambuco, is of a very intense uniform green with the side-stripes hardly visible,
except the elongated seventh which is very white. The mauve medio-dorsal
band is also less pronounced and less edged with white.
The pupa, like some others, is endowed with much nervous agility, and
the force of the exhalation from its big thoracic spiracles is sufficient to blow
away some of the fine sand on which it lies, forming a slight cavity at this point.
This is but a recent observation, and it came with surprise ; for though I have
experienced various audible sounds from different pupae, it had never occurred
to me that a chrysalis could produce an appreciable puff of wind.
Length of proboscis in female moth 5| in., in male 4| in.
37. Cocytius lueifer.
R. & J. p. 59.
Early stages remain undiscovered. From its comparative abundance in
Para as a moth at light on July 8th, and from then till October 1912, its return
from March to May in 1916, and its spasmodic recurrence since, I suggest that
it may be an immigrant from afar, as all attempts to trace its larva locally among
Arvonaceae and other Orders have so far failed. The entire genus are obviously
long and strong fliers, but, whether in fresh or worn condition, I think I am not
beyond the mark when I say that most specimens of lucifer, beelzebuth, and
A. walkeri have, in support of the idea, been picked up off the pavement in a
somewhat lethargic or tired condition. A strange feature to record, unique
among the Sphingidae, so far as I know, and in striking contrast with others of
this genus, is that the female of C. lucifer in Para is almost invariably smaller
in wing-expanse and less robust in general appearance than the male.
Length of proboscis in female moth 4£ in., in the male 3 J in.
38. Amphimoea walkeri.
R. & J. p. 61.
Here I have once again to refer to my remarks on G. lucifer, and suggest
that this large and handsome moth may be drawn from some distance to the
electric lights of Para, where alone I have taken it, about a dozen specimens in
both sexes from March to October 1912, several times since, and generally in
perfect condition. I know also of one specimen caught in Pernambuco. A
general characteristic with many of these big S. American Sphingids, A, walkeri
included, is that they can produce a very audible squeak when handled, like
that of the Death's Head moth in Europe, and recorded in connection with that
species as an almost unique phenomenon. A. walkeri possesses, I believe, the
longest insect-proboscis in the world, measuring as much as from 10 to 11 in.
364 NOVITATES ZOOLOGICAE XXVII. 1920.
Like the genus Cocytius, to which it bears such obviously close relationship, this
almost abnormal development of the trunk, strikingly varied in length with
different species, would seem to indicate that this entire group of moths are
wont to suck honey from flowers with long narrow calices like the Datura. This,
at any rate, has been suggested by both Darwin and Wallace. It may, however,
simply serve the purpose of enabling long-winged and heavy-bodied moths, as
in the case of H. convolvuli, to hover more freely over small flowers like the
jasmine without damage to their wings.
As to the larva and pupa of walkeri, I can but refer to the notes in R. & J.
p. 61, which may possibly describe this species, but I cannot but feel sceptical
in regard to the name of Jatroplta as its food-plant. I may not have sufficient
grounds for saying that I regard it as an unlikely pabulum, but the fact remains
that repeated inquiries among the growers of mandioca and macaxeira, coupled
with the assiduous searching on my own part of Jatropha (Curcas) and all such
Euphorbiaceous plants, has never produced anything beyond the larvae of two
of our commonest Hawk-moths, Erinnyis ello and alope.
39. Protoparce sexta paphus. (Plates T.Z.S.)
R. & J. p. 67.
Abundant in Para as elsewhere. While falling short of a geographical
subspecies, both sexes of the moth are here smaller and blacker, when compared
with the form frequently taken in Lima and those which I have seen from other
places. The larva, too, has a peculiarity here which I have not encountered
elsewhere. When the dorsal and lateral areas are of a uniform green tint, it is
smooth and devoid of hair ; when it is parti-coloured, that is lighter dorsally
above the side-stripes, as when the larva is found feeding on the white woolly
leaves of Solarium grandiflorum, the whole surface is often, but not invariably,
covered with very fine, light hair. I naturally thought at first that I had obtained
two distinct species and figured them both, but I can observe not the slightest
difference in the resulting moths, which in several instances, and in both sexes,
I have been careful to label " smooth " or " hairy," in accordance with their former
larval peculiarity. Both forms are equally common on many Solanaceous
plants, and in no other respects that I can see, beyond what has been mentioned,
do they differ. If the moth appears commonly at fight, the caterpillars are
still more frequently brought to one by friends who find them in their gardens
on the capsicum peppers, the " Bringella," the tobacco and tomato plants.
Besides several species of Jurubeba and Cestrum floribundum, the larva is also
sometimes found feeding in nature on Verbenaceous plants such as Aegiphila
cuspidata, data, and probably velutina. Again, I once took it devouring a hair-
leaved garden creeper with crimson flowers, locally known as " Prima veira,"
and which I am told ranks as a Solanaceous plant, though no one beyond its
mother-moth or the most erudite of botanists would have guessed it.
Length of proboscis in male moth 3J in.
44. Protoparce diffissa tropicalis.
R. & J. p. 75.
A somewhat scarce species in Para, a few moths only having occurred at
light or on tree-trunks. From time to time I have taken solitary larvae, and
Novitates Zoologicae XXVII. 1920. 365
always on species of Solarium, 8. campaniforme, the as-yet-unnamed species
which serves P. perplexa, another common kind with long, rough, pungent leaves,
and perhaps oftener on three of the common Jurubebas. Though obviously
distinct as a species, the caterpillar of diffissa bears but few characteristic features
to differentiate it from a washed-out example of P. hannibal ; while the moth,
especially when worn, may easily be mistaken by the uninitiated for a brown
specimen of P. sexta. The Pernambuco form, however, if one may judge from
a single specimen seen, is much richer in its combination of black and brown,
and would appear to rank as the subspecies difpssa petuniae of Southern Brazil.
Confusion between the larvae of diffissa and sexta can at any rate be avoided
by remembering that diffissa bears an ample horn which is green and rough
and only slightly curved, its head is faintly lined with yellow, and there is no
black edging to the seven light side-stripes. Though I once bred the species
from a larva taken in the Interior of Peru, my figure in the T.Z.S., Plate S.d,
is in error in all these respects, and this particidar specimen, which was found
on wild tobacco and figured, can only have been a strongly-marked sexta, while
the real diffi.ssa escaped my then undiscriminating eye and its pupa got mixed
up in my subsequent travels.
In accordance with its close alliance, the pupa is, as one would expect,
intermediate between sexta and hannibal, though almost impossible to differentiate
with any certainty.
The larva is sometimes stung in the region of the spiracles by a dipterous
fly similar to that which affects P. mossi in Lima, and it is also attacked by a
hymenopterous parasite.
46. Protoparce hannibal. (Plates 1, 2, & 9.)
R. & J. p. 78.
A fairly common species in Para, occurring at light but never abundantly.
Food-plants : Solanaceae, Oestrum floribundum, Solanum campaniforme, and,
as stated by Bonninghausen, trombeta or Datura, two garden species being often
chosen ; frequently also on Aegiphila data and Clerodendron (Verbenaceae).
Though the larva varies in itself, as in its food-plants, with acquaintance
it admits of little doubt as to its identity, being generally of a very intense green
and almost blue on the ventral area, while the seven oblique stripes are broadened
downwards in their whitest portions. The more normal form at any rate is
thus readily distinguished from diffissa, and still more from sexta by the absence
of any black above the stripes, the presence of a few short yellow tubercles on
the thoracic segments, and the ample curved and rough green horn.
Pupa similar to both of the preceding species, but in Para bigger than either.
Proboscis-sheath rather shorter and more robust.
Protoparce perplexa. (Plates 2 & 9.)
R. & J. (1910).
As far as the moth is concerned I have taken but two worn males at light
in 1912. Apparently a very rare species, though, if local, I have reasons for
thinking that the Para region is at least one of its strongholds. Food-plants :
(1) A delicate arboreal Solanum, sp. ?, with small heart-shaped leaves, which
24
366 NOVITATES ZOOLOOICAE XXVII. 1920.
are rough to the touch and light on the under-surface, a widely-distributed
plant, seen abundantly at Porto Velho on the Rio Madeira, but growing only
sparsely in the shade of the forest near Para. (2) A creeping species of Solanum
with bright vermilion berries, rarely noted in the Para matto. (3) Aegiphila
cuspidala ( Verbenaceae) ; one larva only.
The moth at first might be taken for a richly-marked Amazonian form of
scutata, but the larva in all its stages is wonderfully distinct from that species.
It was on the first-named plant in early March 1915 that I eventually took a
single " stung " egg and a very remarkable large black caterpillar with a bright
yellow horn, heavily adorned with setiferous tubercles, held erect and rather
sharply curved down at the tip. The thoracic segments were similarly ornamented
with a thick cluster of exceptionally tall and sharp-pointed tubercles, three being
situated on segment 5, and an odd one marking the right dorsal area of segment 6.
The entire ground-colour of the larva was sooty black, only the last four oblique
side-stripes being faintly indicated in a lighter key and edged above with an
intenser black. The general tone is modified to a gloomy maroon with advancing
growth. My impression at the time was that I had secured a strange melanic
variety of some species ; but having been fortunate enough to possess this strange
caterpillar on eleven subsequent occasions, I find that this description of the
final instar holds good in every detail, even to the irregularity in the position
of the dorsal tubercles, one specimen having an odd one on segment 8 and an
unequal pair on segment 10, surely a unique feature in Protoparce !
Only two of these were found full-grown, and one was full of dipterous
maggots. The remainder were taken in the egg or as very young larvae, and
these up to the end of the fourth instar were always green, the seven side-stripes
gradually increasing in clearness of definition and the colour intensifying to
pure white and lemon-yellow, outlined above with olive. The face up to this
stage is lined with yellow, and the long, yellow-green horn is always exceptionally
erect and is roughened on its upper side with black tubercles.
The first larva obtained formed a dark red-brown pupa similar to that of
P. rustica, with a long proboscis-sheath, and produced a richly- variegated female
moth of perplexa, to my great delight, on April 21st, 1915. After working
methodically for this species from the beginning of 1917, I managed in February,
from the two species of Solanum, above-named, to secure at least a dozen ova
and young larvae, and subsequently lost five through the attack of a small
black ant which infests my house.
Assiduous searching in 1918, a wretched year for almost everything, produced
only one larva in the fourth instar on January 29th, this time a plainer green
variety resembling hannibal (see fig.), found feeding on Aegiphila cuspidata,
and resulting in a perfect male on March 5th. At the time of writing, February
18th, 1919, we appear to have reached low- water mark, and much searching
of the most approved plants in all the likeliest places for miles around Para has
yielded nothing but three eggs of this rare species on one small bush, and all
of them doomed, black centres of corruption, dead yet strangely living, destined
but to render a homage to Baal, the Lord of flies.
Written later. — Towards the end of March I found a small bush of Solanum
completely eaten down, an abundance of black excrement freshly deposited
and typical of this species. The disappointment was great, for I had searched
here before, and from former records I judged that for this year, at any rate.
Novitates Zoologicae XXVII. 1920. 367
the time had gone by. I persisted, however, in the repeated examination of a
particular scraggy Solarium which is still permitted to stretch out its brittle
arms towards the sun in one of the shaded but now disused pathways of Utinga,
and which had yielded ova in 1917.
Here on April 1 1th I was unexpectedly rewarded by finding three oval green
eggs on the under-surface of its sparse leaves, which proved to be those of perplexa,
recently deposited and unstung, and from which I had the good fortune to rear
three perfect moths, a female and two males, before leaving for England on
June 11th, 1919.
As an exceptionally rare and interesting species, it is perhaps worth while
recording the following details of their life-histories :
Ova darkened so irregularly from April 17th that it was feared they were
stung. About noon on the 19th they hatched satisfactorily into well- formed
white larvae with erect black tails. Having consumed their egg-shells, they
readily took to fresh leaves of Solarium and Aegiphila, soon becoming green and
glossy. Then, having more than doubled in size, they cast their first larval
skins after no more than 50 hours. Their subsequent growth was proportionately
rapid. On the 30th two of the three larvae performed ecdysis for the final
instar. This occurred at 9.30 a.m., and from being of a sombre green with 7
clear white stripes, the entire area gradually darkened, while the yellow of the
horn and fleshy tubercles became more intense. At 11.10 a.m., the side-stripes
having now become so dark as to be scarcely visible in the prevailing blackness
of the ground-colour, both larvae turned round and ate up their skins in the
approved fashion ; the third moulting similarly later in the day. On the
following day all three were more intensely black and the side-stripes practically
obliterated. By May 2nd they were much grown, their distended skins appearing
lighter and of a sooty maroon colour, and the side-stripes being once again trace-
able. On May 4th at midnight two of the larvae were laving their bodies with
spittle prior to pupation and the third had finished feeding, making the whole
larval period only a few hours over fifteen days. After burying themselves deep
in wet loam in three separate tins, the first two actually pupated in the early
hours of May 10th, and produced a perfect pair of moths at 9 in the evening
on the 28th of the month. Why the third, a perfect male of rather larger
dimensions which emerged three days later, should have developed more slowly
is hard to say, seeing that no question of sex was involved. It is, however, the
unusual brevity of both larval and pupal periods that is specially worthy of note ;
for 39 days 9 hours from the hatching of the egg to the production of the perfect
moth in both sexes constitutes, I should imagine, a minimum time record for
the genus Protoparce.
Length of proboscis in female moth 4 in., in male 4| in.
55. Protoparce rustica rustica. (Plates 2 & T.Z.S.)
R. & J. p. 84.
Though by no means rare in Para as a moth at fight, and noted from time
to time as a larva feeding on a variety of plants, it appears to be less common
than at Lima. This caterpillar is sufficiently varied in itself and in relation to
its pabula among the Orders of Verbenaceae, Bignoniaceae, Boraginaceae, etc.,
to frequently dupe one into the belief that a new species has been obtained.
368 NOVITATES ZOOLOGICAE XXVII. 1920.
Though already figured in Peru, I have made new illustrations to portray ap-
parently distinct larvae, found feeding at the same time in the Botanic Gardens
on two species of Cordia, one being an exotic from Japan and yielding a larva
of a very intense green. Both, however, on emergence proved to be typical
rustica, and were jjrobably the progeny of the same mother.
In this, as in the majority of Protoparce species, the pupal period is usually
about a month, but the pupa sometimes " stands over," as it is termed, for five
or six months. Certain obvious advantages as well as disadvantages in adopting
this method at once suggest themselves, but the causes which bring it about
are far from obvious. Though other species occasionally behave in this way,
it is, as one would expect, the exception rather than the rule with Sphingidae
in tropical climates like that of Para.
Length of proboscis in female moth 4J in., in male 5$ in.
56. Protoparce albiplaga. (Plates 2 & 9.)
R. & J. p. 86.
Not very common in Para as a moth at light. Larvae found both on Cordia
sp. ? (Boraginaceae) and two species of Anonaceae, including the Biribd (Rollinia
orthopetala) in gardens. Three specific features call for notice, viz. : (1) The
utter dissimilarity of the larva from the ordinary green Protoparce form, albiplaga
assuming an uniformly bluish white ground with cadmium lateral patches
enclosed by a bold design of black in place of the usual side-stripes. Feeding,
as it does, fully exposed on somewhat dull green leaves, no attempt at concealment
on the ordinary lines of protective resemblance to surroundings is possible, and
it forms a truly remarkable exception to the majority of Protoparce larvae which
imitate the green coloration of their leaves, if, as appears, its generic status
is beyond question. (2) The disregard for danger exhibited by the larva of
this species is still further manifested by the gregarious habit, from three to a
dozen or more of the caterpillars being generally found feeding together on the
same branch. This is another high peculiarity among Sphingidae, and finds
but one parallel in these parts in the case of Pseudosphinx tetrio. (3) The
proboscis- sheath of the pupa, which is free like the others, is as stout as that of
rustica, well projected in a rounded curve, but barely half the length.
59. Protoparce dalica.
R. & J. p. 88.
One fine female moth was picked up beneath a lamp in Para and brought
to me by a friend on January 11th, 1913. This, I regret to say, has been the
beginning and, up to date, the end of my acquaintance with this rare and hand-
some species. In such a case, where food-plant and general conditions are not
likely to present any special difficulties, one is left to ruminate as to why it
should be so rare.
64. Protoparce floristan. (Plates 1 & 2.)
R. & J. p. 92.
Moth taken on three occasions only at light in Para and cannot be considered
common. My first and only larva was one found full-grown on February 22nd,
NOVITATES ZOOLOGICAE XXVII. 1920. 369
1916, feeding in the forest shade on a species of Citharexylum (Verbenaceae).
This, though green and bearing a general resemblance to rustica, differed in two
particulars. The side-stripes and numerous spots were of a pronounced lemon-
yellow and the former were unequal, the first three and the seventh being fully
twice the width of the remaining three. The thoracic tubercles and thick rough
horn were also yellow ; there was no pink or red, and the description given by
Burmeister (cf. in R. & J.) is totally incorrect.
The pupa differs from rustica and closely resembles albiplaga in its possession
of a short, stout, though well-projected, free proboscis-sheath. Emergence in
this case was much protracted, the pupal period occupying 4 £ months, and
causing me much anxiety during a pleasant stay with Mr. B. Preston Clark in
Boston. Despite the cold, however, a perfect male moth put in its appearance
on board the New York when nearing Liverpool, and emerged in my cabin after
midnight on June 18th.
Protoparce vestalis.
Jord., Nov. Zool. xxiv. p. 59 (1917).
Two extremely fine males .of this new and interesting species were captured
on lamp-posts in Para on May 6th and June 13th, 1912, and necessitated a
climb on each occasion. By comparison at Tring they are obviously distinct,
being larger than floristan and of a more snowy-white character with a more
defined pattern, and reminding one of the coloration of the Barn-owl.
I naturally hope to come across the species again, but as yet remain as
much in the dark as the rest of human-kind regarding the moth and its early
stages. It is not unreasonable, perhaps, to associate it with Verbenaceae, but
this, after all, is a somewhat " tall order." I may mention, however, that on an
imported Verbenaceous bush, known as " Pao de Angola," growing in a garden
here, I took a full-grown larva of rustica on February 14th, 1919; whereupon
the lady of the house informed me that but a fortnight previously she had
found and killed half a dozen other caterpillars which were eating her bush to
pieces. These, she said, were of similar size and form, possessing a tail, and,
though green in ground-colour, were different in that they had yellow bands
edged with black.
If correct in her description, they cannot have been either rustica or lichenea ;
and I cannot but fear that this dire calamity must have fallen upon heads no
less worthy than those of vestalis or dalica ! She and the gardener promise
not to do it again, cuttings of the plant have been taken, and, so far as life and
opportunity afford, the scent will be followed up.
We append here the description of the larva of a species observed at
Pernambuco.
88. Neogene dynaeus. (Plate 9.)
R. & J. p. 114.
For many miles round the city of Pernambuco, on waste ground, in fields
and meadows and at road-sides, grows a sticky green Verbenaceous herb which
is found useful in dispersing fleas in the neighbourhood of dogs and hens, and is
universally known as "meladinha."
This proves to be the natural food-supply of the above species, which, it
370 NOVITATES ZOOLOGIOAE XXVII. 1920.
Subfamily AMBULICINAE.
137. Protambulyx eurycles. (Plate 10.)
R. & J. p. 175.
Though a plentiful moth in both sexes at light in Para, and occasionally
found at rest by day among foliage, I have only too little to record of its life-
history, having but once, after diligent and repeated searching of Anacardiaceous
trees, discovered a full-grown larva on " tapiririca."
As P. strigilis occurs so frequently and over such a wide area, feeding on
" Cajii " and several different species of Spondias, etc., and has at least three dis-
tinct larval varieties apart from the type, I had several times previously become
convinced that I had at last secured eurycles or its rarer congener goeldii. These
were always figured anew, but always produced typical strigilis. Seeing that
the moth is so often seen on lamp-posts, it is both surprising and disappointing
not to have taken more larvae. I have likewise failed, after repeated attempts,
to induce this species or any other Para Sphingid to lay eggs, though provided
with refreshment, appropriate foliage, and the run of my gauze-covered bathroom.
This species, richer and browner than strigilis, may be described as a little
in excess of it in the matter of size. The larva, as one would expect, is very
similar, the chief differences noted being that the horn was green rather than
blue, and that four of the side-stripes, or what corresponded to them, were
broken up into very irregular patches of ochreous yellow on a uniformly green
ground of rough texture. The pupae of this subfamily, like the last, are formed
in subterranean cavities, probably at some distance from the food-plant.
The pupa of eurycles is exactly like that of strigilis, of a warm, glossy brown,
long and cylindrical, ample and round in the head-piece, but devoid of any
of those peculiarities which characterize Acherontiinae.
Length of proboscis in male moth If in.
appears, can be taken in any month of the year, and would undoubtedly be a
very common moth in the district were it not that its larva is literally decimated
by a hymenopterous parasite. There is nothing to indicate the presence of the
foe within until the final instar, when the maggots appear and spin small creamy
white cocoons all over the moribund form of their victim, standing up on end
like tufts of hair. I once took the larva of rustica on this plant, but neither
" meladinha " nor dynaeus occur near Para.
The larva in nature is generally whitish green with a red mesial line ter-
minating in a fine curved black horn. This is supported on either side by a
dorsal series of round white spots ringed with black. There are additional
black patches, but the extent of these is very variable. With larvae kept in the
dark from early days, the black, in successive moultings, frequently increases
so much as to prevail over the green as a ground-colour. Though drawn on
slightly too robust a scale, four figures were made at full growth to show this
variation ; for in the earlier instars, except in the matter of size, there is but
little essential change from the form and coloration of the adult.
The pupa, like all the rest of this subfamily, is formed in a subterranean
cavity. It is light brown, small compared with the larva, and not very
elegant in form, and possesses a diminutive lobe turned down on the breast
to represent the free proboscis-sheath.
Novitates Zoolooicae XXVII. 1920. 371
142. Protambulyx goeldii.
R. & J. p. 178.
A species accounted rare and local, but recorded from the other side of the
continent in Bolivia, and one which I have myself taken in Para on some dozen
occasions in 1912-13 and several times since. I also took a moth on the lower
Amazon near the Narrows which came to the lights of the boat. The other
specimens were all drawn to electric arc lamps in the city ; most of them were
in perfect condition, and all but one, a lovely female, were of the opposite sex.
A second perfect female was captured at light in April 1919.
This species, named after the founder of the Para Museum, is surely the
most elegant of all our Para Sphingidae in the perfection of its form and in the
bold yet delicate blending of its greens and yellows.
It is a matter of considerable regret that I am unable as yet to record anything
of its early stages. From its obvious alliance to the adjacent species, it can
hardly be other than an Anacardiaceous feeder, and probably possesses a cor-
respondingly similar larval form.
Length of proboscis in female moth 1| in.
143. Protambulyx strigilis. (Plates 3 & 10.)
R. & J. p. 179.
A very common species in Para as a moth at light.
Larvae also most frequently observed on saplings of " Caju " and " Taperiba "
(Anacardiaceae), the denuded stalks or frass on the sand beneath revealing the
particular spray where the larva has been feeding, and to which it clings head
downwards by two pairs of claspers only, geometer-wise.
As with eurycles, the front portion tapers off extremely towards the head,
while the claspers on segments 7, 8, and 9, being retractile, are seldom used
save when the caterpillar is eating or moving its position. The horn, which is
of a light cobalt blue, is well erected and slightly turned up, and it is long and
rough but of light construction.
The body is generally of a vivid green, well ringed and rough in texture,
sprinkled over with fine yellow dots and a series of the same in line to mark the
side-stripes. These are less conspicuous than in Protoparce, except the seventh
leading up to the horn, which is always an ample white band. Three special
varieties of the larva have been noted, the first two at least seeming to depend
exclusively upon the particular species of food-plant chosen by the moth. They
may be described thus : (1) Utterly devoid of any spots or stripes except the
white seventh. This form is invariably and exclusively associated with a fern-
like species of Anacardiaceae (genus Rhus), the leaves of which are of a very
smooth and glossy green without protruding ribs. I presume that this form
of the larva by being similarly plain is the better disguised, but it is little short
of miraculous by what process it accomplishes the feat. (2) Green with yellow
dots like the type and small inconspicuous blue spiracles, which are constant
in all specimens. It differs in possessing a short broad band of pure white
outlined with brown, as a remnant of the full stripe-pattern. This is situated
immediately above the line of yellow dots on segment 7, and it sometimes
possesses a similar band on segment 8. This form, on parallel lines with var. 1,
372 NOVITATES ZOOLOGICAE XXVII. 1920.
is similarly restricted to the very crinkled dark green leaves of a somewhat
uncommon species of Spondias growing in the Utinga water-works region, and
its harmony with the plant is emphasized by the possession of a slightly deeper
tone of green. (3) Though the "Cajueiro " or Cachew tree often produces the
type, a light pink and yellow form variegated with touches of warm brown is
sometimes found on it, seeming to imitate the coppery tint of its newly-expanding
leaves.
A nervous irritability is a character in common between this species and
eurycles, as already noted for Cocytius antaeus, the larva when disturbed wagging
itself violently from side to side.
The pupa, like the former, is of a warm glossy brown, possessing large
eye-cases but no free proboscis-sheath, and outwardly resembles a thin Oryba.
Length of proboscis in female moth 1 J in., in male 1 J in.
145. Amplypterus gannascus.
R. & J. p. 181.
146. Amplypterus ypsilon.
R. & J. p. 182.
147. Amplypterus palmeri.
R. & J. p. 183.
Here I have so little to say, not yet having had the good fortune of tracing
the early stages, that I have perforce to deal with all three species in one short
paragraph. Though scarcely abundant in Para, gannascus and palmeri both
occur with comparative frequency at the city lamps. Of ypsilon I took a perfect
female at light on July 17th, 1912, and this constitutes, I believe, a record for
the species in this part of the world. Though there is an abundance of Lauraceas
plants in the district, and among them several species of Oreodaphne or Ocotea,
the suggested food-plant, and though the moths generally appear in the pink
of condition, as if freshly emerged, I have repeatedly failed after many attempts
to track any of them to headquarters. When professional collectors on their
travels do succeed in rearing a moth from its larva, it is regrettable that they
so often pay scant attention to the plant, and are not precise in description
nor careful enough, when the opportunity offers, to acquire information as to
identity. From the rich herbarium at the South Kensington Museum this is
generally to be had for the asking at the hands of the courteous and learned
Professor in charge of the Botanical Department, or one of his assistants.
This completes my notes on the Ambulicinae for the present. They are
decidedly meagre and unsatisfactory, but I have hopes of being yet able to
learn something more of the early stages of the Para representatives of this
particularly beautiful subfamily.
Subfamily SESILNAE.
This third great subfamily of the Sphingidae is represented in Para by no
fewer than 16 genera and 47 species. Of some 36 of these I now know something
about the early stages ; on the remainder my notes for the present must neces-
sarily be brief. I must, however, deal at somewhat greater length with Isognathus,
and, referring to the close relationship which its species obviously bear to
Pseudosphinx tetrio, I would note that the latter differs outwardly from Isognathus
Novitates Zoolooicae XXVII. 1920. 373
in three particulars (see R. & J. p. 352) — viz. its greater size, an entire absence
of yellow in the moth, and the colour of the pupa, which is red-brown with black
lines instead of orange, brilliantly delineated with black, so marked a feature
with all the species of Isognatkus, and shared to a less extent by Erinnyis and
others. The very obvious alliance between the two genera is emphasized by
the following considerations :
(1) The common adoption of the various species of Plumicra as food-plant,
to which all but three species appear to be restricted in nature.
(2) The tendency observable on the part of the larvae of several species of
Isognatkus, which is the normal habit of Pseudospkinx, to live gregariously in
small numbers.
(3) The insistence of a transverse belted design, exhibited in the early
instars of at least five species of Isognatkus, and maintained by swuinsoni subsp. ?
as well as P. tetrio to the end of the larval period.
(4) The strange and somewhat garish arrangement of colours which char-
acterize the larvae of both genera.
(5) The repetition of a couple of sharp spurs on the anal flap, together with
the universal whip-like and flexible black tail, terminating with a minute bifid
fork, and more or less clothed with tiny setiferous tubercles.
Though I have had the good fortune to trace out the life-histories of all the
species yet known except rimosa, and even add a new species or two to the genus,
it is apparent that there are obscurities still, and that the present sequential
order of the species is wrong throughout.
Reverting to the white larva of Protoparce albiplaga with its black and
yellow design, considered in relation to the larvae of Pseudospkinx and Isognatkus,
may I be allowed to theorize for a moment, and suggest that the colour-scheme
of all these larvae, and their tendency towards the gregarious habit, present
us with an interesting case of reversion to, or possibly the retention of, ancestral
type ? With albiplaga it seems to me possible that, while most of its other
structural features have advanced on evolutionary lines exactly parallel to those
which have produced its fellow-species, and modified the great majority on the
Darwinian principle of Natural Selection, this species and the Isognatkus group,
to take prominent examples, have preferred to face danger in the broad light
of day with a contempt for duplicity. I may mention that the very young
larva of albiplaga bears an extraordinary superficial resemblance to /. swainsoni,
being belted white and black with a long curved black tail and a couple of tall
black spurs on the anal flap.
These spurs appear to be a feature which was once as universal in Spkingidae
as the tail, but, while tending to die out, has not yet quite vanished, and is
therefore most noteworthy as indicating a common, if distant, ancestry. The
importance of this consideration lies in the fact that, while these anal-flap spurs
are still so pronounced a feature in Isognatkus and are strongly developed in
Protoparce albiplaga, being marked up to the end of its larval period by a couple
of reduced black tubercles, the feature is nevertheless obviously shared by such
comparatively distant species, but only up to the end of the second instar, as
Cocylius duponchel (very slightly in cluentius and antaeus), and even pronouncedly
in Protambulyx strigilis.
Speaking generally, larvae seem, in some mysterious way which we cannot
pretend to delineate, to have been controlled by the obvious advantages and
374 Novitates Zoological XXVII. 1920.
extra security gained by resemblance to surroundings ; by being green, for
example, and looking like leaves, or brown and resembling twigs and dead leaves,
or by hiding away altogether, instead of, as aforetime, as I assume, living in
gregarious batches.
If the idea be feasible at all, my supposition is that all these species and
many others throughout lepidoptera which have adopted or retained " warning
colours," seem, as it were, to endorse the principle that, notwithstanding a certain
amount of incidental loss and destruction, for them at any rate " honesty is
the best policy." Therefore it is that their larvae, being bright and showy, and
consequently not much to be desired by the predatory foes of their kind, become
an even more formidable spectacle when congregated in numbers.
Again, many young Sphingid larvae belonging to different groups show a
significant feature in common in the first instar.
I refer to the primitive tail, which at this period is long, rough, bilobed and
flexible. With the majority this organ becomes speedily modified, but with the
Isognathus group, though proportionately enlarged or reduced, it is in its essential
features retained to the end of the larval period. In one species, /. swainsoni,
so little change takes place that the full-grown larva, a zebra-like white and black
creature with a touch of ochreous- yellow, is hardly more than the baby caterpillar
magnified. My further supposition therefore is that, in Isognathus as a genus
and in swainsoni as a species we have the nearest approximation to ancestral
form. This genus accordingly seems admirably placed in Sesiinae, the central
subfamily of Sphingidae, for it emphasizes the radial, in preference to the im-
possible linear, system of classification. If, however, it should be thought better
to instance a large, hardy, and robust Hawk-moth, at once common, widely
distributed, and invariably gregarious, the species which satisfies all conditions
is ready at hand in Pseudosphinx tetrio, as the standard type or nearest modern
representative of the ancestral Sphingid form ; for it, too, in the adult larval
stage is only a great big baby, and from its well-known abundance and wide
distribution it affords a better starting-point or basis for the argument than
swainsoni.
Once again, if the ancestral Sphinx formed a brightly-coloured and striped
pupa beneath a web on the surface, as does Isognathus to-day, or a highly lustrous
brown pupa with black design like P. tetrio, affording scope for development,
it seems quite to accord with my theory that some of the offshoots should have
adopted the subterranean method for the safety of their pupae, thus becoming
modified to a plain brown without design, and that others, like Xyloplianes,
while still spinning a fragmentary web on the surface, should have found it
expedient to sink into obscurity by producing pupae which resemble wood,
dead leaves, or pieces of bone. I may be suggesting the impossible, but on
the chance that some enthusiastic entomologist, who is also an evolutionist
expert, may be sufficiently interested to look into the matter and elaborate its
details, I have propounded my romance, and I can only trust that it may not
be considered far-fetched.
287. Pseudosphinx tetrio. (Plates T.Z.S.)
R. & J. p. 353.
One of the commonest moths in Para as in other parts of the continent,
its immense black, yellow-ringed, and red-headed larva frequently showing up
Novitates Zoolooicae XXVII. 1920. 375
in gardens and public squares on the Frangipanni tree. A large batch often
completely strips the tree of its leaves, and this gregarious habit, already alluded
to in connection with P. albiplaga, as exceptional in Sphingidae, can, I think,
only be explained on the supposition that the possessor of bright warning colours
enjoys some immunity from predatory attack. These great larvae may often
be seen sunning themselves on the trunk and twitching their heads about in a
seemingly nervous fashion. A few strands of silk are spun beneath fallen leaves
to form the puparium, and the highly glossed pupa is marked with black lines,
especially on the wing-cases, as in Isogjiathus.
The female moth is considerably larger than the male and of a lighter
grey, and both sexes, which come freely to light, show no special local variation.
I have never found the species attacked by parasites.
Length of j>roboscis in female moth nearly 2 in., in male 1£ in.
Genus ISOGNATHUS.
As I have occasion only too frequently to deplore my inability, after prolonged
residence in the country, to record anything about the early stages of certain
species both rare and common, may I be allowed a small boast in respect to
Isognathus, where I have had an almost continuous run of good luck ? This genus,
as it seems to me, is one of the most interesting, and yet, so far as my acquaintance
with its species goes, is one where the greatest confusion prevails and entire
revision is necessary. I will therefore record my experiences in rough chrono-
logical order for what they are worth, and point to the conclusions to which they
seem to lead.
I began with P. tetrio and /. sicainsoni (see T.Z.S. p. 92), finding both species
in 1918 in the Interior of Peru feeding on " caucho de monte," a tree which I
wrongly described as a wild Ficus, but is in reality a species of Plmniera (not
Plumeria, as in R. & J.), Apocynaceae.
In my first month after reaching Para, July 1911, I took the single, white-
banded larva, which produced a crippled moth like swainsoni and which, until
more material is available for comparison, can, I think, only be regarded as the
local caterpillar form of this species, as rare here as it was common there.
Returning to Para in 1912, I restarted my investigation of the Plumierae,
sucuuba, fallax, phagedaenica, etc., and, though I never chanced on the same
caterpillar again, I very frequently took young and matured examples of
leachi, the larva of which up to the fourth instar is very similar, but totally
unlike in the last stage.
The next to turn up was a single full-grown larva of excelsior on one of
the same plants, different in important respects from leachi, as the figures show,
but obviously an adjacent species with a longer tail and designed on the same
model. From that day to this I have taken the larvae of menechus in all stages,
twice on Artocarpus integrifolia (Moraceae), but in every other case on Plumiera.
Journeying to Manaos, the examination of the local Plumierae at once yielded
three species, a full-grown leachi, eight tiny caricae which I successfully reared to
the moth on my return to Para, and a new species referred to below. In 1917
I again took leachi and caricae at Porto Velho, and caricae once again at Per-
nambuco in 1918, all being found exclusively on Plumiera. Before this, however,
I had accidentally come across a single larva of an Isognathus on Allamanda
376 NOVITATES ZOOLOGICAE XXVII. 1920.
cathartica which turned out to be scyron ; this led to the finding of so many
others, that I was soon aware that it was undoubtedly the commonest species
of the genus in Para. Reverting to my entirely new species, two young larvae
in the second instar were found feeding on a narrow-leaved species of Plumiera
at Taruma near Manaos in January 1913. One died in moulting, the other fed
up during my return to Para, pupated, and duly emerged on March 20. I
subsequently found more young larvae and some eggs in February and March
1917, not only on the shores of the Taruma lagoon but on the banks of the Rio
Negro nearer to Manaos, and in November of that year I rediscovered the species
at Nazareth on the Rio Faro, in the State of Para. I have now bred it on some
eight occasions, and it has been designated mossi in my honour by Mr. B. Preston
Clark, of Boston, Mass.
On two different occasions odd larvae of caricae were discovered among
the rough vegetation lining the beach at Chapeo Virado, Mosqueiro, twenty
miles north down the river ; and now, as recently as the middle of March 1919,
I find the species to be very abundant there, a few being taken on Plumiera,
but the majority, upwards of a hundred in all stages of growth, occurring on small
bushes of Allamanda growing wild in the sand close to the water's edge. Though
other Isognathi will grudgingly partake of the alternative pabulum in captivity,
this appears to be the only species to be found in nature on both Plumiera and
Allamanda. On the other hand, while thriving equally well on either, it appears
to be strangely fastidious in regard to locality and to the precise position and
growth of the plant chosen. Out of my 90 Para species caricae is the only one
that has not yet been noted in either larval or imaginal condition close to the
city. This is strange, for the species is obviously prolific, and its two food-plants
are abundant here. By a comparison with P. tetrio and the various species
of Isognathus in regard to early stages, as well as in the moth, caricae is perhaps
the most difficult to place accurately. Seeing that its larval form and habits
resemble those of tetrio, and that its pattern as a moth, as stated in the Revision,
is more ancestral than that of the other species of Isognathus, it would seem to
be more correct to place it next to tetrio — that is, at the beginning rather than
at the end of its genus. It should, however, in this position, be regarded as
an offshoot, for otherwise it interrupts what would appear to be an equally
natural sequence from tetrio to swainsoni, etc.
My last species is one which I have recently taken in abundance at Per-
nambuco, and which my friend T. T. Dyer has still more recently had the good
fortune to capture here in Para as a male at light on February 24, 1919, thus
adding a species to our already extensive list of local Sphingidae which must be
as rare in Para as it is common in Pernambuco.
My first acquaintance with it was as a moth at light in this latter place
in May 1918, and I took it at the time as a worn but exceptionally grey specimen
of scyron. Finding out my mistake, and returning thither in September, I
explored all available plants of Plumiera and Allamanda, and was almost at
once rewarded by the discovery of many larvae in all stages, found feeding in
gardens on Allamanda cathartica, but never once on Plumiera. These larvae
were so similar to scyron and so different to those described by Schaus and
Gundlach (R. & J. p. 358), as found on Plumiera and producing rimosa, that I
was again led to associate my Pernambuco species with scyron and regard it
as an extreme local race of this species. This I am now convinced cannot be
NOVITATES ZOOLOGICAE XXVII. 1920. 377
the case, if it be only by the finding of a single moth, Mr. Dyer's perfect grey
male, alongside the typical brown and only known form of scyron. Again,
though the moth tallies with the description given under the head of rimosa
papayae in R. & J. p. 359, I am strongly of opinion that the first name is
erroneous and the second simply misleading, the unhappy hit, as it seems, of
Boisduval in 1875 ; for in regard to the latter, the subspecific term papayae only
puts one off the scent, as in my experience and that of others not one species
of the entire genus ever touches Carica papaya as a food-plant. The same
remark applies with equal force to Linne's name caricae, a mistake stereotyped
since 1764. Possibly it was the discovery of the larvae of the common Erinnyis
ello and alope, as more or less close relatives feeding on Cacrica papaya, which
has led to this unwarranted assumption.
It may here be noted that the entire group is all but exclusively associated
with Apocynaceae, and that Plumiera belongs to that Order and not to Euphor-
biaceae. In appearance and habits as an Allamanda-ieeder, the new species is
obviously more closely allied to scyron than to any other, and must be granted
an independent name. Since writing the above, Mr. Preston Clark has received
my consignment of a dozen perfect bred specimens from Pernambuco. He is
convinced that this is a new and distinct species ranking between rimosa and
scyron, which he proposes to call allamandae. Finally, I gather that congratulans
has already dropped out of the category of true species, and is now regarded
simply as an extremely dark subspecies of rimosa from Cuba.
Piecing then together all the scraps of information which have accrued
concerning this group, more especially in so far as they relate to early stages
and food-plants, may I take the liberty of suggesting the following order
as a nearer approximation to the true sequence ? — 1. tetrio. 2. caricae. 3. swain-
soni. 4. leachi. 5. excelsior. 6. menechus. 7. mossi. 8. rimosa. 9. allamandae.
10. scyron. While retaining the old numbers for reference, I feel bound to
adopt this order in my present notes so as to avoid further confusion and not
interrupt certain natural sequences.
295. Isognathus caricae. (Plate 3.)
R. & J. p. 360.
Not found as a moth, and taken only at the distance of 20 miles from Para.
The young larva on emergence from the egg is almost black, but after moulting
bears six lateral patches of white, a dull red head, a yellow patch at base of tail,
and a row of dorsal bristles.
In the succeeding instars considerable development takes place, with an
ever-increasing number of intricate markings in blue and red and finely pencilled
lines in white and yellow, as shown in the figures. It is to be noted that the
customary white belts in this case are hardly more than a couple of fine white
rings near the interstices of each segment, first on a dull black ground, becoming
intensely black and velvety in the final instar. In the redness of its head, the
comparative shortness and thickness of its tail (which, however, generally bears
a white ring about the middle), and in the coloured patch at its base, caricae
undoubtedly approximates to tetrio. In the strong yellow ring on segment 2,
the yellow lateral skin-folds and sundry other marks, it shows a departure from
all the rest.
378 Novitates Zoologicae XXVXI. 1920.
Among those taken in the last instar at Chapeo Virado many were brilliantly
adorned on the back of each segment with square patches of carmine-red, giving
them an exceptionally rich and handsome appearance. In the matter of size
and agility, they reminded one much of tetrio, readily falling to the ground when
approached, exuding large drops of a yellow fluid from invisible apertures in
any part of the skin, and without any apparent damage (noted as a characteristic
of the entire group, but to a less degree), and making off with great alacrity
over the grass and hot sand from those defoliated stems and gnawed stalks of
Allamanda where they had been feeding and basking in a blazing sun.
A large and free cocoon of strong red-brown silk is spun among grass and
debris on the surface of the earth, and the pupa, which is formed in three days,
is of a distinctly lighter straw- yellow than that of any other species of the genus.
As though to emphasize its difference from all the rest, even in later life,
the dark band bordering the hindwing of the moth, so characteristic a feature
throughout Isognathus, is in caricae merely represented by some seven or eight
dark radial streaks on a light yellow ground.
Length of proboscis in both sexes 1 § in.
289. Isognathus swainsoni subsp. ? (Plates 3 & 4, and compare T.Z.S. swainsoni,
Plate 8.)
R. & J. p. 355.
This may be a new and hitherto undescribed species, one nearly full-fed
larva which pupated but produced a cripple in August 191 1, and one wasted moth
in the following year, being all that I have yet to record. This moth, with a
very broad dark border on the yellow hindwing, resembles sivainsoni, which
species I bred in Peru from larvae with no trace of red on their heads, and had
rather shorter tails ; moreover, the white predominated over the black.
My Para larva was essentially black with white belts, and as red as P. tetrio
on head, plate, anus, and claspers to the end of its caterpillar existence. With
such scant material, however, I am inclined for the present to regard both moth
and caterpillar as simply the eastern geographical race or a local form of sivainsoni,
a specimen of which is recorded as having been taken at electric light in Para
by Dr. Goeldi and sent to the Bern Museum. It is evidently very rare here,
as all attempts, oft-repeated throughout the district, to retrace this remarkable
and highly conspicuous larva on the " sucuubas " of the matto, or the Frangipanni
of gardens, on which latter it fed in captivity, have so far failed.
Pupa formed in a surface cocoon, and in itself indeterminable from leachi
and the rest (except caricae), the various species showing little if any essential
difference inter se beyond the matter of size. When living they are all of a
bright and lustrous cadmium-yellow, with numerous tar-black streaks marking
the wing- sections, clearly defined and somewhat variable big spots on head and
thorax, and finer transverse lines and spots on the abdominal segments. They
become uniformly dark before emergence.
288. Isognathus leachi. (Plates 3 & 4.)
R. & J. p. 355.
Quite a common species at light in Para. Like others of the genus, frequently
taken as a larva on various wild species of Plumiera, and will readily take to
Frangipanni in captivity,
NOVITATES ZoOLOGICAjf XXVII. 1920. 379
The young black-and-white-belted larva with ochreous extremities in the
first three instars appears to be identical with sivainsoni. A great change,
however, takes place in the fourth instar, the ground-colour lightening to mauve
and the white belts becoming creamy, rounded off before reaching the legs and
claspers, and being finely outlined in black. A still more remarkable change
in the final instar produces an entirely distinct-looking larva, the head being
salmon-pink shaded on the face by umber-brown, the back adorned with a
series of irregular X-like marks and the sides with light-coloured ovals. A
couple of light longitudinal stripes divide the dorsal from the lateral areas.
The entire ground-colour is now of a delicate violet, legs black, claspers ochre
in black settings, and all the light patches are finely outlined with black.
No parasitic attack observed.
Length of proboscis in male moth If in.
294. Isognathus excelsior. (Plate 4.)
R. & J. p. 359.
Moth common at light in Para in 1912 and a few every year since, but never
so abundantly. The larva, only once taken at full growth on sucuuba, was
similar to leachi, but differed in the following respects : tail bluish at base, stouter,
rougher, and nearly twice as long, quite the longest of the genus, in fact ; ground-
colour dark steel-grey ; dorsal and lateral patches, together with interrupted
stripes, claspers, and upper half of legs of a warm ochreous colour, the dorsal
patches more V-like, being cut off posteriorly by the transverse black belts
which complete each segment ; anus light but adorned by nine dark marks, a
couple on the flap representing the hard tubercles or spurs which are shared
by all these species alike. On the analogy afforded by swainsoni and leachi, it
is highly probable that in the early instars excelsior partakes of the same black-
and-white- belted design which characterizes those species. As the moths have
nearly always appeared in fresh and perfect condition, I fail to understand the
extraordinary rarity of this larva by comparison with leachi and menechus, unless,
like the latter, it possesses some alternative and possibly preferred natural
food-plant.
Length of proboscis in male moth 1 £ in.
291. Isognathus menechus. (Plate 4.)
R. & J. p. 356.
Frequently bred from larvae found on the " sucuubas " of Para, and on
several occasions also I have taken it feeding on the leaves of the Jaca tree,
Artocarpus integrijolia (Moraceae), but, as a moth, only once or twice has it
occurred at light. This difference in the degree of susceptibility to the attrac-
tiveness of light with species known to be common, and which are yet but
seldom thus ensnared, is very extraordinary. Not less strange is the observation
frequently made that certain arc lamps, apparently equally attractive and
well-placed, should be variously selected by different kinds of moths, one, for
example, being the rendezvous of a host of common Sphingids, another being
the particular lamp where the greatest variety of ISynlomidae have occurred,
and so on with other groups, while the rarer or more exceptional Sphingidae,
380 NOVTTATES ZOOLOOICAE XXVII. 1920.
such as Oryba kadeni and achemenid.es and the species under consideration (though
here it is not rare), will, like the usher of the poet, be found " remote from all,"
the same species of moth, for example, occurring time and again in the same
position and on some particularly favoured white wall that catches the light
of a street-lamp. Though not without its exceptions, of course, this small
phenomenon has been so frequently noted by my friends as well as by myself
that I make a passing mention of it, for it seems to suggest that artificial light
may, in accordance with its degree of intensity, quality, or peculiar waves of
vibration, extend a varying attractive influence upon different species and even
upon different families and groups of insects. It may be for some such subtle
reason that here and there we meet with an exception even among the Sphingidae,
as a family so notably drawn to light, but with instances occurring, like menechus,
where the impelling rays find but little response in its optic retina.
The larva of menechus, with but slight modifications, once again corresponds
closely with leachi, for example, in that its first three instars are characterized
by the black-and-white-belted design with ochreous extremities, while the fourth
and fifth instars differ immensely from this, from one another, and from others
of the genus at these particular stages. To describe these changes in all their
details is difficult and perhaps unnecessary, as the main differences can readily
be gauged by a careful comparison of the figures. It is, however, interesting
to note that the oval patches, which adorn the sides of leachi and excelsior in
their final stages, are prepared for in menechus by a series of finely curved black
lateral lines in the third instar, perfected in the fourth, and merely enlarged in
the final stage. The dorsal area in this species develops marks of a more elongate
and subdivided character, increasing depth of colour, and in general foreshadows
the linear or longitudinal stripe-formation which reaches its climax in mossi
(sp. nov. Clark).
WhUe excelsior possesses the longest tail, menechus would seem to exceed
all others of the genus, except perhaps caricae, in the bulk and weight of its
full-fed larva, occasionally falling but little short of a small P. tetrio. A larva
found on jaceira (the Jaca tree) once produced dipterous parasites.
Length of proboscis in female moth If in.
Isognathus mossi. (Plates 4 & 10.)
Isognathus mossi Clark (1919).
Two larvae in the second or third instar were taken on my second expedition
to Manaos in January 1913, and were presumed to be those of rimosa, a species
which at that time I had never seen. These were found feeding on a narrow-
leaved and possibly undescribed species of Plumiera which grows plentifully
on the white sandy shores of the Taruma lagoon and the Rio Negro near to
Manaos.
It would fill a chapter to narrate the details of my subsequent endeavours
to obtain more of this unknown rarity : how various kind and interested friends
in Manaos in 1917 arranged special expeditions to Taruma for me by their private
motor-launches ; how, before leaving for Iquitos, I secured a stung egg and then
two diminutive larvae, only to have them ruthlessly destroyed as soon as I
NOVTTATES ZOOLOGICAE XXVII. 1920. 381
got on board by a miserable horde of ants ; how on my return I got three more
hardly bigger, and next day found the corpse of one sucked dry by a bloodthirsty
spider, etc., etc. But suffice it to say that in the end I managed after prolonged
and diligent search — and my thanks will ever be due to Messrs. Sutton and Fair-
weather and Captain Roxo — to procure some 5 or 6 more in their second, third,
and fourth instars. Leaving Manaos on March 22, I at last succeeded in pro-
tecting them from foes and feeding them up to good-sized larvae on the boat
returning to Para, and finally I had the extraordinary good fortune to rediscover
the species at Nazareth on the Rio Faro on the same voyage.
As the Cuyabd had to stop here for some hours to take in timber, I availed
myself of the opportunity of going ashore and searching for fresh fodder. This
place is situated on the boundary line between the States of Para and Amazonas,
and from the former locality is nearer to Belem by some 350 miles. The
outlook was propitious, for the white sandy beaches lining water as black as the
Rio Negro were well clothed with a varied scrub vegetation. Exceeding my
utmost anticipations, I was again successful, for not only did the same particular
variety of Plumiera grow there plentifully, but my new Isognathus was actually
there as well, showing a remarkable constancy to a special type of plant and
locality. In great jubilation I returned to my boat with not only enough fresh
sucuuba to last for the rest of the voyage, but with an additional larva found at
full growth on the stem of a plant and a couple of eggs, which latter, however,
were stung and useless, as I could see at a glance. I now had 8 larvae, and all
but 1 fed up well, pirated, and in Para three weeks later 7 perfect males and
females of this very distinct new species emerged.
The pupa is of the normal Isognathus colour, pattern, and form.
The moth may be described as intermediate in size between menechus and
rimosa, rounder and broader in wing and of a more sooty grey than any of the
others, while the strong black band on the yellow hindwing is fully as broad as
in menechus or excelsior.
The newly hatched larva, which very readily falls from its leaf, is dead
black with a few touches of white in its posterior half and a black tail of almost
its length curved forward. After moulting, it possesses a distinctly chequered
design in black and white.
In the third instar this is maintained, the longitudinal white lines on a
black ground being interrupted by the transverse black rings of the interstices.
The extremities are ochreous, as in menechus, and its black tail with a white ring
corresponds with that species in its form and length. The chief differences
noted in the last two instars were the amalgamation of the spiracular patches
into one continuous broad lemon-white band, the increased yellowness of head
and plate, the anus conversely growing duller, while the ground-colour becomes
a warm chocolate-brown with longitudinal stripes of Indian red and lemon-white
adorning the back and sides.
Isognathus allamandae. (Plate 10.)
Isognathus allamandae Clark (1920).
Having already dealt at some length with this species, I need not repeat
what has already been said on p. 376. Let me, however, emphasize a few points
which distinguish the larva. The pattern throughout, like that of scyron and
25
382 NOVITATES ZOOLOGICAE XXVII. 1920.
the later stages of mossi, is one of numerous longitudinal stripes and lines in
grey and white, the spiracular band being more or less definitely pink. Compared
with scyron, which it most closely resembles, it is more clearly lined but paler
and greyer, scyron developing from pale grey into a dirty brown with a subdued
brown chequered design not found in this species. Small black and yellow
marks adorn the front of the plate. The dark grey tail is exactly like that of
scyron — that is, both are equally short in proportion to the full-grown caterpillar
when contrasted with a species like leachi, for example, and both are twice ringed
with white.
It is a dull and dowdy creature, and in the final instar, like scyron, it always
hides away in the shade during the heat of the day on the dry stems of its food-
plant or on some adjacent object as dull as itself. On Allamanda cathariica in
gardens and on a closely related wild species alone did I ever find it, and, if
present at all, it generally occurred in fair numbers, the same moth having
obviously deposited a number of eggs separately on different parts of the plant.
The favoured situation was where the Allamanda was growing as a verandah
creeper, and here from the varied size of many larvae it was no less obvious
that one beheld the progeny of more than one mother. Rather loosely-spun
cocoons were found among the dried portions of ferns growing next the wall
beneath, many containing empty shells, but some newly formed, and not a few
containing old pupae riddled with holes by the exodus of parasites.
The pupa itself, though more slender in proportion to the size of the moth,
is in colour and pattern constructed on exactly the same lines as scyron and the
others. Though all the above observations were made in Pernambuco, Mr.
Dyer's single male, taken at light in Para on February 24, 1919, provides sufficient
justification for the inclusion of this species as one of the Para Sphingidae, no
matter how rare it may be, and apparently is, locally.
I note that Schaus says, in reference to rimosa inclitus, that the larva changes
to pupa in from 10 to 14 days. This is surely a mistake, 3 or 4 days at" most
with all my species, and so far as I can remember with all other Sphingidae,,
being the limit of time during which the larva lies in its puparium' before the
final moult, and most of them emerge in little more than 3 weeks later.
290. Isognathus scyron. (Plates 2 & 4.)
R. & J. p. 356.
This is undoubtedly the commonest and, except for the one just dealt with,
the smallest species of Isognathus in Para, the moth frequenting lamps and the
larva nearly always to be obtained in the public and private gardens of the
city by searching the leaves and stems of the lovely Apocynaceous shrub or
creeper Allamanda cathariica. With this, like the former, it appears to be
exclusively associated, never in nature having been taken on Plumiera. The
ova and young larvae when grey are easily found on the under-surface of leaves,
but in the last instar, being of an earthy-brown colour, they successfully hide
away during the day on the dusty-brown stalks or in curled-up dead leaves.
Having studied its development from the egg, several of which are often laid
upon the same plant, the following notes may be of interest.
1st instar. — Sooty black, the young larva when examined under the lens
exhibiting strong characteristic features. Head dirty white above, clean below,
NOVITATES ZOOLOQICAE XXVII. 1920. 383
and divided by a lateral black belt, as if masked. Segment 2 with a couple of
prominent black dorsal tubercles surmounted by fine hairs and backed by a
transverse white belt which connects two subspiracular white bands. These
bands, which are very white in the anterior half, become hardly visible from
segment 7 to 11 inclusive, and appear to be sooted over. The upper parts of
segment 12 and the anus are clear white sprinkled with black dots. Below on
the black anal flap are situated the couple of strongly developed black spurs,
which are reduced in altitude inversely with the growth of the caterpillar, but
always present. Many fine bristles adorn the back, and the curved dark grey
tail, which at this period is fully three-quarters of its entire length, is rough and
distinctly bi-lobed at the extremity.
In instar 2 the dorsal and lateral areas become grey with black dots.
In instar 3 a lighter grey is assumed, bearing a distinct medio-dorsal black
line. The light lateral band is now uniformly white, contains the spiracles, and
is bordered above with black. The plate behind the head is now yellow and
adorned with two small black tubercles and two other black spots. The tail
now and in the two succeeding instars is ringed near the base and near the tip
with white.
In instar 4 the design of the adult larva prevails, the colour in individual
specimens varying between a light vinous and an umber-brown freckled with
darker touches, the head and plate a dull yellow, the back sombrely lined, and
the sides relieved by the spiracular bands, which are now of a very dirty or
clouded pink and contain light spiracles.
The pupa, which is commonly found spun under moss on tree-trunks, is
rather stouter than the former species but otherwise identical : and it is
occasionally found riddled by the holes of parasites.
Length of proboscis in female moth 1} in., in male 1 in.
Genus ERINNYIS.
Here I have a note to record in relation to the pupae. As with Isognathus,
so also in Erinnyis, is there a standard generic pattern of pupa to which the
species wonderfully approximate and which ought not to be confounded with
the former. While allowing for their variability in size, the type is undoubtedly
like Isognathus in general form and colour, and is similarly adorned with black
stripes on the wing-cases and with short transverse black dashes on the ab-
dominal segments, but it differs in certain important respects : ( 1 ) The yellow
colour generally inclines to a mahogany red and both extremities tend to be
suffused with black. It must here be remembered that the bright colours,
whatever they originally were, are seldom as bright after the emergence of the
moth, and the precise tone or tint cannot be gauged from the empty pupa-shells
of a collection. (2) The black design on head and thorax, if apparent at all,
is much less pronounced and perfect. (3) It is longer for its size, or, in other
words, somewhat narrower in proportion to its length. (4) The cremaster,
though sharp-pointed, is invariably stouter at its base. (5) Its surface, though
glossy, is rather less highly glazed. By a general grasp of these features it will
be seen that several of the descriptions given in the Revision of the pupae of
Isognathus and Erinnyis are very deficient, and some actually erroneous,
384 Novitates Zoologicae XXVII. 1920.
A loose-spun but ample cocoon, similar in all respects to Isognathus, is
formed by all these species under dead leaves or concealed among herbage on
the surface.
296. Erinnyis alope. (Plate T.Z.S.)
R. & J. p. 362.
Commonly observed as a moth at light in Para or as a larva feeding on
Hevea, Carica, Curcas (Jatropha), Manihot, and other Euphorbiaceous plants.
If green in the early instars, it is generally of a dark brown richly mottled in the
final stage of the caterpillar with a yellowish ventral area, and is readily dis-
tinguished from ello by its more prominent tusk-like blunt horn, which is smooth
and light-coloured.
Its well-known thoracic patch of colour is shared in common, though in
varying tones of red and black, by ello, oenotrus, and crameri, but not by lassauxi
and obscura. Puna very similar to ello but rather longer.
Length of proboscis in male moth 1J in.
297. Erinnyis lassauxi, forms lassauxi and omphaleae. (Plate 10.)
E. & J. p. 363.
Moth not uncommon at light in Para, and now frequently bred from ova
and larvae found on a garden creeper with sweet-scented white flowers, known
locally as " angelica doar " (Asclepiadaceae), but never on Morrenia, as recorded
by Burmeister, who also gives the same food-plant for oenotrus. I doubt if he
was correct in either case, and he most certainly could never have seen the larva
of lassauxi when he said that it was very much like that of ello, for nothing more
different in adjacent species could well be imagined ! One might be excused
for anticipating that such would probably be the case, but the fact is far different.
So utterly unlike was my first-found larva, that I was unable even to guess its
genus, or do more than rank it in Sesiinae. Only when it formed a pupa out-
wardly identical with alope did I judge that it must be lassauxi, for I had already
taken the larvae of all the other local species of Erinnyis except domingonis,
and this was twice the size. Not having my figures by me now, I can only
describe it very generally by referring to its truly remarkable mimicry of the
food-plant, the white-knobbed swollen process on the thoracic segments exactly
simulating the end of a flowering stalk from which the flowers had fallen, these
white lobes representing drops of the congealed milk or latex which is so char-
acteristic of this plant and other Asclepiae, and the four side-patches of light
brown in strange design on a sage-green ground, inclining to milky-white dorsally,
admirably repeating the twining green stems with their ever-present light and
brown scars. Not a mark but counted for something in the general scheme
of resemblance to surroundings ; and if this does not happen to be its natural
or original food-plant, it can doubtless be sustained by a very similar wild species
with large leathery leaves growing in the matto. After the first accidental find
I have frequently taken it in gardens, but only on this plant, the larvae, except
when very young or when eating, generally reposing in a strangely contorted
attitude among the stalks.
As regards the moth, and in response to the suggestion made on p. 364 of
the Revision, I may state that the two forms /. lassauxi and /. omphaleae with
NoVITATES ZoOLOGICAE XXVII. 1920. 385
the cinnamon-rufous patch of varying size on hindwing are both 'very distinctly
present here, two fine specimens of the latter being entirely without the black
spots on under-surface of abdomen. As I used to take both forms of this moth
in Chanchamayo, Peru, it is obvious that they do not represent geographical
races or subspecies.
Length of proboscis in both sexes If in.
298. Erinnyis ello. (Plate T.Z.8.)
R. & J. p. 365.
Enough has already been said in the general introduction and elsewhere
of this extremely common species, and the only additional touch of interest
that I might here record is that I once found the larva in its fourth instar in
Barbados feeding on the leaves of the deadly " manchineel " (Euphorbiaceae),
and that its horn in this case, hitherto unnoticed, was like a knob, swollen but
tipped at its extremity, and capable of a small degree of inflation and contraction.
Length of proboscis in both sexes 1J in.
300. Erinnyis oenotrus. (Plate 10.)
R. & J. p. 367.
Of very frequent occurrence as a moth at light in Para, less often observed
as a larva, and taken only for the first time in July 1917 on a small bush of
Zschokkea sp. ? (Apoc), growing in the Para Bosque. In November of the
same year I took 5 more at Porto Velho on the same plant and on a species of
Echites with dark green and rather hairy leaves, as rare here as it was abundant
there. On this same Apocynaceous plant I also took several larvae of Pachylia
resumens, to be referred to again.
In early days the larva is of a uniform light green, the dorsal and lateral
areas divided by the customary pair of light stripes leading to a long, curved
tail. In the later instars it has both green and grey-brown' forms, the latter much
freckled throughout with tiny brown touches and a double series of brown spots.
Though distinct enough from the others to the eye, it is difficult to describe beyond
saying that it is like ello, but proportionately longer and more slender, and often
rests on the brown stalks with three pairs of claspers retracted, giving it a very
geometer-like appearance. Its horn, from being like a knob with a tip in the
fourth instar, is reduced in the last stage to the merest sharp point, exactly on
a par with ello. The colour of the pupa is rather brighter than that species,
and is less obscured by black at the extremities.
Length of proboscis in female moth 1 J in., in male If in.
301. Erinnyis crameri. (Plate 7.)
R. & J. p. 368.
As common a species as a moth at light in Para as the former, but in the
larval form only seldom seen. The first was discovered accidentally in August
1914 as a pale green larva feeding on a species of Tabernaemontana {Apocynaceae),
and this led to more finds on the same plant and to one on a kindred species.
Its tail up to the last instar and its transverse light belt on the thoracic
segments recall ello ; there are ;also the customary pair of light stripes dividing
the dorsal from the lateral area.
386 NoVITATUS ZoOLOGICAE XXVII. 1920.
In the final stage the larva generally assumes a uniform ochreous-brown
coloration, inclining to blue and freckled with light spots and black dots. The
claspers are ringed with velvety blue-black, the face and legs lined with black,
and the interstices of the thoracic segments adorned with two belts of bright
vermilion. The second of these is centred with black, but neither of the belts
is in the least degree visible when the larva is at rest, reposing like the last species
geometer-wise with retracted claspers and stretched across the fork of a bough,
a perfect stick among sticks and most easily overlooked.
Pupa very similar to ello.
302. Erinnyis obscura obscura. (Plate 7.)
R. & J. p. 368.
A fairly common species at light in Para, and once again but seldom seen
in the larval condition. This, however, was first found in May 1913, and has
occasionally been taken since by searching a somewhat inconspicuous small-
leaved creeper, Gonolobus sp. ? (Asclep.). These occur in both the green and
grey-brown varieties which characterize ello, and, though a smaller species, and
without the dorsal patch of colour on the thoracic segments, it bears a general
resemblance to that species. Like all the others of this genus, its anterior claspers
are retractile, and it protects itself by adopting the same geometer-like attitude
when at rest.
The pupa, though a little lighter in tone and only half the size, is
practically identical with lassauxi, i.e. with rather more black than oenotrus
and less than ello and alope.
303. Erinnyis domingonis.
R. & J. p. 370.
Much rarer than the preceding species in Para, taken freely at light in 191::
but only very occasionally since, and the larva remaining undiscovered. From
its obvious close relationship to obscura, it is natural to assume that the larva
is constructed on much the same lines as that species, and that it will eventually
be found to be also associated with Gonolobus or some kindred plant in the Order
Asclepiadaceae.
305. Grammodia caicus. (Plate 7.)
R. & J. p. 371.
An interesting species not hitherto recorded for Para, the moth occasionally
coming to fight, and the larva, after the first accidental find jat Val de Caes, four
miles down the river, being frequently taken in small numbers on two species
of Echites and once on Zschokkea (Apocynaceae). The larva is a somewhat
plain creature, varying in colour between pink, light brown, and pale olive-green,
and possessing a straight, erect horn up to the last instar, when there is hardly
more than a hump. With the dorsal area enclosed by two stripes from face
to tale, it at once suggests Erinnyis, but there are some evenly distributed light
spots, and in form it is really more that of an elongate Koctuid.
The cocoon is in all respects like that of the previous genus, a moderately
stout-spun web amongst vegetation on the surface. The pupa, too, is extremely
NoVITATES ZOOLOGICAE XXVII. 1920. 387
similar to that of Erinnyis, but the light yellow ground-colour is more banded
and spotted with black and it is distinctly less glossy.
306. Pachylia ficus. (Plate T.Z.S.)
R. & J. p. 373.
Again we come to a species so widely common and of which so much has
already been said in the general introduction and elsewhere that there is little
more to add. Though not so often drawn to light as might be expected, its
great fat green larva is nearly always to be found on the neatly cropped Ficus
benjamina trees which adorn the avenidas and pracas of the city. It occurs
here also on several other species of Ficus with foliage of very diverse character,
and it is sometimes obtained from the leaves of the common fig-tree in gardens,
but here, at any rate, I have never found it on Artocarpus or Cecropia, the forms
of plant-life so greatly preferred by its congener syces. The strange lichenous
variety of ficus also sometimes occurs, and the caterpillar, when it has assumed
the vivid orange coloration prior to pupation, is constantly being picked up
in the road by non-entomological friends, who are quite disappointed to learn
that they have not in this case been privileged to add a rarity to the collection.
307. Pachylia syces syces. (Plate T.Z.S.)
R. & J. p. 374.
Not uncommon but rarely taken as a moth at light in Para. When met
with in the larval condition, it has always been found associated with Moraceae,
Artocarpus integrifolia, Ficus sp. ?, and Cecropia, and too often is it already
doomed to destruction by dipterous as well as hymenopterous parasites. I
have now frequently bred the moth, and found it a very common species in
Pernambuco on the Jaca tree which so largely prevails there.
The larva, after assuming its characteristic series of black belts, comes down
to earth and is then frequently seen by the natives. On those occasions when
the crevices of the roots of its own tree offer sufficient inducement to it to stay,
its large, glossy brown, and vivacious pupa may readily be found in a loose-spun
cocoon under stones and dead leaves.
308. Pachylia darceta.
R. & J. p. 376.
Though the female is rarer than the male, the moth in both sexes is of
frequent occurrence at the electric lights of Para, and I once took a male similarly
in the streets of Manaos.
This large species, however, is one which up to date has baffled all my attempts
to elucidate the mysteries attaching to its early stages ; and after having had
my faith shaken by what has recently come to light in regard to the larva and
food-plants of resumens, I incline to the view that darceta, too, is a somewhat
distant cousin, is not to be found associated with Moraceae, and may possibly
feed on a species of Davilla (Dilleniaceae). This, at any rate, is the favoured
pabulum of such allied genera as Aleuron and Enyo, and frass, too big for their
species but appropriate for darceta, has been noted beneath such a plant, sug-
gesting the idea. Some of these creepers growing in dense thickets are naturally
388 NOVITATES ZOOLOGICAE XXVII. 1920
very difficult to explore fully. On the other hand, darceta may be associated
with some completely different type of growth and live well above one's head.
That some very large species are thus accustomed to inhabit the upper branches
of enormously high trees, utterly beyond the reach of the most skilled climber,
is too apparent by the frequency with which one discovers the excrement in
some void place on the ground beneath, sometimes of great size and possessing
peculiarities of form new to the eye.
Length of proboscis in male moth If in.
309. Pachylia resumens. (Plate 10.)
R. & J. p. 376.
Moth in both sexes of very frequent occurrence at light in Para as elsewhere,
but the larva rarely seen. Indeed, being misled by the statement that it was
known, and that it resembled a small edition of ficus (vide Revision, p. 37S), on
whose authority I know not, I wasted much time during my first five
years in Para in exploring Ficus trees of all descriptions ; but the " smaller "
larvae resembling ficus always grew big, and were, in fact, that species in every
instance.
Once again, therefore, one has to deplore the lack of careful and thorough
observation on the part of some moth-collectors in foreign parts, who too readily
assume that they have seen the larva of the moth they have caught without
having taken the trouble to rear a single specimen. In point of fact, the larva
of resumens, beyond being green, is not in the least like ficus, and could never
be confounded with that species by any one who had really seen it. The yellow
side-stripes are not only more numerous, but they form a series of V's at the
mesial line and lead up to the horn. In ficus and syces they run contrariwise,
and terminate abruptly with the light longitudinal lines which enclose the dorsal
area. In resumens this area, though lighter, is not clearly divided off by lines
at all. The long, turned-down tail of early days is replaced in the last instar
by a tiny point surmounting a prominent hump. Again, the texture of the skin.
the swollen nature of the thoracic segments, and the black-and-yellow ringed
base of the legs on segments 3 and 4, give resumens far more the appearance
of being a closer ally to Perigonia or Sesia than to its neighbours in Pachylia.
The cylindrical glossy dark brown pupa with its long, sharp-pointed cremaster
seems also more to reproduce the form of Epistor than that of Pachylia. Finally,
in its food-supply it appears to be limited to certain species of Echites in Apo-
cynaceae, sharing one with Leucorhampha, but ignoring at least three other
varieties. It was in Porto Velho that I first took the larva in November 1917
feeding on a species with dark green and rather hairy leaves, and which appears
very rarely here. In Para, however, I have twice subsequently taken it by
the railway line feeding on a distinct species of Echites with large, yellowish,
and rather glossy leaves.
Length of proboscis in male moth 1 in.
We come now to the only two known species of Oryba, and if a proud mother
is justified in exhibiting her bonny twins to an admiring world, it is with a kindred
satisfaction that I present my two golden babes, partly because they are both
so handsome and interesting in all their stages, and partly because, after keeping
NOVITATES ZOOLOGICAE XXVII. 1920. 389
me waiting for a long time, they both ultimately rewarded my patience by
coming to light in more than the technical sense.
310. Oryba kadeni. (Plate 5.)
R. & J. p. 379.
By no means uncommon in Para, this exceptionally handsome moth with
its rich combination of green, yellow, and black is much drawn to light, both
sexes often being found in the neighbourhood of electric lamps by day, though
not so often captured. This species and its congener seem to be endowed with
an extra degree of nervous vitality, and make off in a wild flight, especially
when approached in bright sunshine. I first figured the larva from two specimens
found in the Interior of Peru, feeding on some very long-leaved plant of the
Order Rubiaceae. Both pupated, but subsequently died owing to the rigours
of a four days' journey to Lima. I correctly diagnosed the species at the time
through the enormous eye-cases of the pupa, kadeni possessing, I believe, the
largest eyes of all lepidoptera known ; but with the lack of absolute certainty
I decided, on the expert advice of my friend Dr. Jordan, at Tring, to defer the
publication of the figure. The matter is now settled beyond doubt by the
recurrence of the larva on very many occasions in Para in all stages of growth
on a long-leaved species of Palicourea with bunches of red and white flower
{Rubiaceae).
Though normally as yellow as a sunflower, with large black spots and stripes
and, when full-grown, as big as Acherontia atropos, making it a very conspicuous
object, I have twice found a brown-and-white-banded variety of the adult larva,
so different in design as to suggest another species. Indeed, I thought that I
had then obtained achemenides until its identity was revealed on emergence.
The young larva is pale green with a whip-like bifid tail, and, with modifications
of this appendage, a pale yellow or pink-brown colour is assumed, both tone
and design gradually intensifying and forecasting the adult stage. How this
most striking caterpillar can have been passed unheeded by collectors of moths
and butterflies in the American tropics for so long is a puzzle, and it seems to
suggest that those who are engaged in stocking our museums might occasionally
do better service and deepen every one's interest in the study, their own included,
if they would oftener leave the net and search for larvae. In my own case it
is only by so doing that I have taken many of my best Sphingidae, and out of
four at least that are absolutely new to science, two have never, been taken on
the wing and only bred from the larvae. There are few things in nature to
equal, still less to excel, even in the very moths which they produce, the larvae
of Sphingidae in their superlative elegance of form and curve, blend of colour,
and perfection of imitative design. The trouble of course is that they do not
offer the same facilities for preservation as do the moths. A blown caterpillar,
especially when large and green, as so many of the Sphingidae are, becomes
too often a parody of its former self. Better success is met with at times in
species that are ornate and deeply coloured, and when care has been taken not
to over-blow them. But to interest a wider public, the accurate depiction of
the living larvae on their food-plants in their characteristic attitudes at all stages
is obviously the great ideal to be aimed at. How many strange and wondrous
forms of life have been seen only to be at once forgotten, or occur simply as a
390 NoVITATES ZOOLOOICAE XXVII. 1920.
fading reminiscence in the mind of the solitary observer who has been privileged
to wander through the forest and swamp of the tropics ! Such deficiencies can
and should be met by more descriptive notes, more hand-drawing, or more
photography, with facilities for reproduction on a more extended and organized
scale than has hitherto been attempted.
The puparium of kadeni is a subterranean cavity, the walls of which are
supported by a slight amount of silk. The pupa is of a bright mahogany-brown,
stout but elegantly curved, with enormously large eye-cases and a very strong,
broad, but sharply-pointed cremaster.
Length of proboscis in female moth I in.
311. Oryba achemenides. (Plate 5.)
R. & J. p. 379.
This moth, though reckoned a rarity, is by no means uncommon at light
in Para, but it is difficult, except by rearing, to obtain in perfect condition. It
seems particularly fond of settling on overhead wires and in other exalted and
impossible positions. It sits, like kadeni, with its wings spread at a wide angle,
and flies off like a bird when approached. The resemblance between this species
and the former is by no means so close in its early history as a general similarity
in the moths would lead one to expect. Indeed, the parallelism between the
two species hardly extends beyond the fact that they both have yellow cater-
pillars with brown varieties, and that they are both Rubiaceous feeders. This
species, however, as I at last discovered after long and fruitless searching on
Palicourea, only feeds on Ourowparia, a strongly-built creeper which generally
grows on the outskirts of swampy matto. The plant possesses glossy ovate
leaves and big curved thorns like the claws of a vulture, and goes by the local
and most appropriate designation of "Unha de gaviao." The tails of both Orybas
when young are on the model of Isognathus, being whip-like and flexible, dark
in colour, light-ringed, and distinctly bi-lobed at the tip. The evolutionary
progress of the caudal appendage is, however, different, the tail being more
sickle-like and prominently erected in the fourth instar of achemenides, suggesting
the thorn of its food-plant, and becoming only a small hard button in the final
stage ; while with kadeni, the long, slight, and curved-down tail of the fourth
instar lapses into a tiny sharp point in the last stage. Both species possess
very smooth velvety skins, but the difference is otherwise very great, segments
4 and 5 in achemenides, especially in the last three instars, being swollen out
laterally in diamond-fashion to an enormous extent, giving the caterpillar a
very strange appearance utterly unlike kadeni. The latter is almost uniformly
cylindrical and of a deep cadmium yellow with black spots, while achemenides
is marked with 0 white and 8 green irregular patches in lieu of the lateral oblique
stripes directed towards the tail. The medio-dorsal line is represented by a
series of dark marks at the interstices, and the dorsal area is defined by two
irregular green lines from the face to the horn, the ground-colour being of a
delicate lemon-yellow. The equally common brown variety is of course identical
in form with this, but the strong combination of light and dark colour on the
head and anterior segments, together with a big white square spot on the rich
brown of segment 4, constitute very striking differences, and give this innocent
creature the general appearance of being formidable and snake-like.
MOVITATES ZOOLOGICAE XXVII. 1920. 391
In the pupa the diameter of the eye-case is distinctly less than that of
kadeni, and the cremaster is shorter and blunter.
312. Leucorhampha triptolemus. (Plates 6 & 9.)
R. & J. p. 381.
This species, though but rarely seen as a moth at light in Para, has proved
to be fairly common and widespread in the district in its larval condition, and
merely needs to be searched for on its favoured food-plants, two species of
Echites (Apocynaceae), growing in special localities. Its near of kin, ornatus,
strongly prefers the leaves of " Pao de colher" (Zschokkea sp., Apoc), growing
in the shade of the forest, but as both species occasionally take the alternative
pabulum, an element of uncertainty is produced, for they are extremely alike.
Indeed for some time I confused them, and in the original sketch for this article
I wrote as follows : "If these names really represent distinct species, I can only
say that both occur in Para, and that the line marking their specific differences
is an exceedingly fine one in all stages of their being. Both, for example, feed
on various species of Echites, and the moths, which to my eye only differ in
the presence of a bronze-green scaling in ornatus, and more extended yellow
belts between the abdominal segments in triptolemus, proceed from larvae and
pupae in which I am unable to detect any distinction beyond that which is
incidental ,to individual variation."
Such was my view at the time, but I am now fully satisfied that the species
are distinct, and while still insisting on their close relationship and great similarity,
especially in the larval stage, subsequent experience enables me now to affirm :
(1) that the egg of triptolemus is distinctly smaller than that of ornatus, the
latter being exceptionally large, and from the outset, as it were, rightly fore-
shadowing a larger and more robust insect, though to the eye the ultimate differ-
ence may be but slight ; (2) that the larva of triptolemus, though identical w^th
ornatus in average size, form, habits, colour- scheme, and essential markings,
is generally browner and more heavily marked ; (3) that triptolemus has a
plain, lemon-coloured variety with light green markings, similar to achemenides
but not yet noted in ornatus ; (4) that the pupa of triptolemus, while appearing
identical, nevertheless differs in that it is generally smaller, has a rather finer
cremaster, and, most important of all, that this cremaster under the lens is
shown to be possessed of two small divergent points not found in ornatus ; and
(5) that the moth of triptolemus, reverting to the question of colour and scale-
distribution, is of a cooler brown shade with a minimum of green scaling, possesses
a longer and finer silver streak, is less elegant and pointed in the apex of forewing,
and narrower or more squat in the breadth of hindwing.
The description which I now quote was written in November 1915 for the
larva of ornatus, but as it applies equally well for triptolemus and must be regarded
as doing double duty, I prefer to insert it here. The larva is quite one of the
most remarkable of living creatures that I have ever seen, a perfect Aaron's
rod, combining in the most novel and striking way the principles of protective
resemblance with an aggressive snake-mimicry. When at rest as an adult
caterpillar, it hangs by two pairs of claspers in the vertical from the stem of
its food-plant, and appears to be nothing but a broken branch covered with a
dull, creamy white lichen. A strange black chequered dorsal design, with a
392 NoVITATES ZOOLOGIOAE XXVII. 1920.
gradual intensification of the grey on certain segments completes the deception.
The wonder, however, is if possible exceeded when, on being disturbed, this
marvel of creative evolution endeavours once more to deceive by turning into
a snake, and in quite a different way to that adopted by Xylophones or even
by its fairly close relative Madoryx pluto. Though this wonderful transformation
wants to be seen in life to be fully appreciated, I may explain briefly that the
effect is produced by the creature turning itself over and exhibiting its ventral
area, which is adorned by a broad band of dark olive-green with the three anterior
sets of claspers completely withdrawn and scarcely visible. The thoracic seg-
ments, which are always swollen, become puffed out laterally to an exaggerated
extent ; a pair of black eyes on segment 4, hitherto concealed and situated
behind the now recumbent and wholly inconspicuous legs, open out ; the cheeks
appear to be adorned by yellow scales with black edges ; and the fraudulent
notion that one is beholding merely the head and neck of a formidable, if small,
snake is carried to a nicety by the rigidity of the curve adopted. Then, as if
to mesmerize, a swaying side-to-side motion is kept up for an appreciable number
of seconds, before the creature, seeming to realize that an attack is no further
contemplated, gradually closes its false eyes and relapses once more into diurnal
slumbers. That this mimicry of the fore-part of a small serpent, if mimicry it
be, for it is hard to give it any other name, should be chiefly produced on the
ventral surface, a feature peculiar in itself, and that every detail should so
contribute in perfecting the deception, is altogether remarkable. •
Prior to pupation the lighter tones of the larva turn to orange. It then
spins a moderate cocoon among debris, and changes in three days to a uniformly
dark and glossy pupa. My first specimen (of ornatus) at this particular period
produced, to my utter disgust and disappointment, 72 writhing dipterous
maggots, the presence of which it was impossible to foretell, as the demeanour
of their over-burdened host was in all respects normal and it bore no external
defacement. I naturally had no peace until I had explored the matto far and
near for its food-plant and tracked down my larva once again.
Length of proboscis in male moth li in.
314. Leucorhampha ornatus. (Plates 6 & 10.)
R. & J. p. 382.
Though not really scarce in the larval stage throughout the humid and
shaded parts of the matto, it is rarer than the preceding species, and I never
remember to have seen this particular moth at the electric lamps of Para, which
can scarcely fail at times to attract it like its congener. For a full descrijjtion
of this species and its intimate relationship with triptolemus, it is necessary
carefully to study the foregoing. It is there apparent that one general account
must suffice for the adult larvae of both species ; and though there may be
many small points of specific difference which I have overlooked, I believe I
am not far wrong when I assert that the descriptive notes of the earlier instars
of ornatus given below apply very closely in detail to the corresponding stages
of triptolemus.
After my first accidental find of a stung larva I discovered empty egg-shells
on Zschokkea, and full ones later on on a kindred Apocinaceous species (sp. ?)
NOVITATES ZOOLOGICAE XXVII. 1920. 393
with a free-flowing white la^ex. These first tiny larvae had obviously perished
soon after emergence.
I then procured similar eggs on the near relative of Echiles known as Am-
blyanthera versicolor, but these were filled with the minute grubs of hymenopterous
parasites. Ultimately I succeeded in rearing this highly interesting and
remarkable caterpillar to its moth from a single big green egg, found on the
under-surface of a young fresh leaf of the first-named plant, and the process
has several times been repeated since. The notes that I then made are worth
recording, for they well exemplify the extraordinarily rapid growth and develop-
ment which takes place in very many species in this part of the world ; the
entire cycle of changes' from the hatching of the egg to the formation of the pupa
being exactly 24 days, while 18 days more sufficed for the production of a perfect
female moth.
Green egg developed band of crimson 2 days before hatching.
December 19, 1915, at noon, plain light green larva emerged, tail shortly
becoming red-brown and mobile. Alimentary duct visible as a medio-dorsal
line. Did not appear to eat much beside egg-shell, but grew appreciably and
prepared to moult on evening of December 21.
December 22, at 10 a.m., moulted, first instar having been passed in the
remarkably short period of 72 hours. Colour soon changed to grey-green, and
by 8 p.m. on December 23 was of a glossy pale maroon. Undersurface dark,
dorsal area graduated from light to dark sienna. Tail held in trailing posture
and dark at tip. Geometer-attitude first adopted when in repose.
December 25, at noon, moulted second time. Colours intensified, a couple
of black ocelli showing on the dorsal area of third thoracic segment, losing their
intensity in the next instar, and being replaced by a much more highly elaborated
pair on the ventral surface of the same segment. Tail of increased length,
flattened laterally about centre.
December 29, at noon, moulted third time for fourth instar. Colours more
intensified, especially dark on ventral area, the snake-representation and general
pattern of the adult larva being anticipated in many details. Tail like a curved
knife-blade.
January 3, at noon, moulted fourth time for final instar, as already described
for triptolemus. Tail now exchanged for a minute light red point.
January 9, at noon, exactly 21 days to the hour, light colour changed to reddish
orange, and at midnight began to spin cocoon among leaves and earth. Shortly
orange colour faded out again.
January 12, during afternoon, pupated, the pupa resembling triptolemus, but
being without the minute bifurcation at the tip of the cremaster which charac-
terizes that species.
Length of proboscis in male moth 1 J in.
316. Madoryx oiclus.
R. & J. p. 383.
Of this species I have but little to tell, having only managed to pick up a
stray and not very perfect male on the pavement beneath an arc globe in one
of the main streets of Para on July 8, 1912, and another perfect male at light
in April 1919. However, my friend Mr. T. T. Dyer, with an increasing enthusiasm
394 Novitates Zoological XXVII. 1!I20.
for studying the lamps, has had the good fortune, to take a couple of nearly
perfect females, but neither of us have yet learnt anything about its early habits
or its larva, which is doubtless as weird and snake-like as its relatives. From
its apparent intimacy with bubastua, it is not improbable that it is a Tecoma
feeder ; but with such a labyrinth of green as we possess in these parts, one can
only deplore the lack of that precise knowledge in regard to its particular tree
and locality, which, for the time at least, bars all further progress.
Length of proboscis in male moth 1J in.
317. Madoryx pluto. (Plate 6.)
R. & J. p. 384.
This species can hardly be described as common in Para, but I have secured
a good series of the moth in both sexes from electric lamps and bred a few others
from larvae obtained on four or five occasions. The short descriptions of the
larva and cocoon given in the Revision on pp. 383 and 385 are quite correct. I
am very sceptical, however, when I see it described as a feeder on Jussieva
(Onagraceae), of which we possess many varieties, ever serviceable to Pholus
fasciatus and cams, but not one that would ever provide sufficient space or pro-
tection on its stem for the formation of the cocoon of pluto, as I have found it.
Its two chief food-plants here appear to be Miconia minutiflora (Melastomaceae)
and " Cafe rana " sp. ? (Vochysiaceae). The statement that its " stout chrysalis
resembles that of Pseudosphinx telrio " is wholly incorrect, and should be replaced
by its " long and elegant chrysalis is dead black with ochreous interstices between
three of the abdominal segments." The pupa of pluto, like all adjacent species,
is exceedingly nervous and lively.
The larva in its final instar, if the championship among frauds be already
won by the Leucorhampha species, nevertheless runs them closely, and takes
a very high second place in the perfect success of those devices resorted to in
first simulating the living stalk or stem of its food-plant, and then by endeavouring
to terrorize one into the belief that one is gazing at an open-mouthed snake
with red jaws and a couple of fierce, blue-black eyes set immediately above
them. This particular effect is produced entirely on the dorsal area by the
larva lowering its head towards its legs, puffing out its thoracic segments (not
laterally this time), and exhibiting these wonderfully brilliant touches of external
ornament which at all other times when the caterpillar is sleeping or even when
it is eating or in motion are entirely concealed within the interstices of its seg-
ments, and looks a perfect stick of a light brown coloration. Though I secured
two photos, to take its portrait as a snake in pencil and paint was an exceedingly
difficult task, for it would never maintain the attitude for a sufficient length
of time, and soon got tired of even repeating the hoax for the edification of my
much-impressed friends. Writing now in April 1919, this species seems to have
become as rare and unprocurable as almost everything else in these parts ; and
though it may seem fanciful, I cannot help feeling that the general dearth of
iepidopterous life, which appears to prevail throughout northern Brazil and
is noted by all friends of the soil, must be due to some widespread epidemic on a
par with the influenza among human beings, and may possibly be attributable
fundamentally to that same malign influence, whatever it be.
In support of the view. ] mention that a number of full-grown larvae
NOVITATES ZOOLOGICAE XXVII. 1920. 395
of different genera — such as Protamhvlyx, Episior, and Xyloplianes, apparently
otherwise healthy and unmolested by parasites, have recently been found hanging
dead from their stalks.
318. Madoryx bubastus butleri.
R. & J. p. 385.
This is not a Para moth, and is one of my six interlopers referred to on
p. 357.
Consequent upon a short visit to the West Indies in July 1915, I am able
here to insert a brief note in regard to what I take to be this species, but possess
now no material for comparison.
(1) The moth is distinctly smaller and browner than oiclus, which, rather
than pluto, it chiefly resembles.
(2) The larva, though I never saw it, obviously feeds on what is locally
known as the Whitewood cedar, Tecoma leucoxylon (Bignoniaceae), an abundant
tree in the Islands of St. Vincent, Bequia, and St. Lucia.
(3) It spins an ample web or cocoon and covers it with scraps, like pluto
does, in the crevices of the trunk of that tree.
(4) Its pupa is of a lighter brown than that of pluto. with light interstices,
but is smaller.
(5) From the frequency with which I found the old cocoons, it is obviously
a common species in these three islands at least.
I can say nothing of its larva, as I was only able in the short time at my
disposal to procure two full cocoons, from which perfect moths emerged within
the next ten days. This unfortunately occurred after a day's exploration of
the ruins of St. Pierre, Martinique, and as I had no killing-bottle they both got
damaged beyond repair.
320. Hemeroplanes nomius.
R. & J. p. 388.
A species of frequent occurrence, especially the male, at the electric arc
lamps of Para, and once similarly obtained at Manaos, but as yet remains untraced
in its early stages.
Length of proboscis in male moth J in.
321. Hemeroplanes pan.
R. & J. p. 388.
Length of proboscis in male moth J in.
324. Hemeroplanes parce.
R. & J. p. 390.
Both these species, like the former, are known to have a wide distribution,
and both occur with equal frequency and in perfect condition at the electric
lights in Para. Though comparatively small moths, they are stout enough to
proceed from moderate- sized larvae, and the mystery surrounding their early
stages is very hard to account for. Their obviously close alliance with inuus
396 NOVITATES ZOOLUGICAE XXVII. 1920.
makes it probable that they are at least among that large number of species
that favour Apocynaceous plants as a food-supply for their larvae, but as
yet nothing can be discovered. It is unfortunate that among our Brazilian
Spkingidae, so far as my experience goes, not a single caught female of any
species will ever consent to lay in captivity. Though treated with every con-
sideration in my bathroom, each one in turn batters itself to pieces and dies
full of eggs.
325. Hemeroplanes inuus. (Plate 7.)
R. & J. p. 391.
In 1912 more frequently met with than the three foregoing species as a
moth at light in Para. The egg is laid upon the tender leaves of " Pepino do
matto," Ambelania tenuiflora (Apocynaceae), young or small trees in open places
seeming to be preferred. The larva, which I first obtained in May 1914, has
been found very sparingly since by working such trees at this time of year. It
is elongate in shape after the manner of Erinnyis, and not at all snake-like as
in the foregoing genera. The head is large, the ground-colour plain green, and
a couple of light lines from face to tail enclose the dorsal area. These lines are
of a clear lemon tint on segments 2 and 12, and the sides are relieved by orange
spiracles. The tail, which in the early instars is pale green with minute touches
of black, long and trailed, becomes a stout, curved, and well-erected blue-black
horn in the last stage. From this description of inuus it seems highly improbable
that the larva referred to in the Revision on p. 387 was that of its near relative
pan. Excrement small, light green, and neatly hexagonal. The pupa is of a
plain and glossy dark brown, and is formed beneath a slight web on the surface
of the earth after the larva has turned pink and wandered away from its food-
plant.
Length of proboscis in male moth § in.
328. Aleuron carinata.
R. & J. p. 395.
Here I have nothing more to record than the capture of a single female moth
on March 24, 1917, which was attracted to the lights of my boat at Parintins,
near the boundary line between the States of Amazonas and Para. The species
has not yet turned up here.
331. Aleuron chloroptera.
R. & J. p. 396.
Evidently a rare species in Para, my first perfect moth having occurred at
light in November 1915, and only six specimens having been noted since, four
of them being captured by Mr. T. T. Dyer.
From the habits of the three following species, I think it probable that
the whole genus are Dilleniaceous feeders with preferences for particular species
of Davilla. The early stages of chloroptera, however, still remain to be discovered.
N0V1TATES ZOOLOGICAE XXVII. 1920. 397
333. Aleuron iphis. (Plate 7.)
334. Aleuron neglectum.
R. & J. p. 398.
Both species have now been fairly frequently taken at light in Para and
up-river, but cannot be regarded as common here.
The larvae, from their general resemblance to one another, were not dif-
ferentiated at the time, and I can therefore only show one figure, which for the
present must stand for both species. They were found in August and September
1914, feeding upon a comparatively scarce form of Davilla (Dilleniaceae), which
is longer in leaf and less rough than the common D. rugosa, and have not been
taken since.
This latter plant, a kind of creeping bush which grows very abundantly
at the roadside in many open sunny places, will serve as an alternative food-plant
in captivity. Larvae green or brown, possessing both the enclosed dorsal area
and oblique side-stripes leading to the tail. The thoracic segments are swollen
out laterally, the legs on segments 3 and 4 spring from bright crimson patches,
and the horn evolves from the sickle-pattern, as shown in Enyo japix, to a mere
point in the last instar. The pupae are of a straw yellow like those of Isognaihus,
but naturally much smaller and with less black ornamentation, and are similarly
formed beneath a web on the surface among debris.
Length of proboscis in male moth f in.
335. Enyo japix japix. (Plate 7.)
R. & J. p. 399.
Probably not rare, but only occasionally taken at arc lamps in the city.
This species vies with its congener in being the smallest Sphingid in Para. The
larva, which resembles the foregoing, is green or pink- brown, possessing
exaggerated thoracic segments and a sickle-like tail, evolving to a mere point
in the last instar. I have but twice taken it feeding on Davilla rugosa (Dill.),
and once on a kindred species in June 1919.
Pupa yellow with black lines on exactly the same model as the previous
species of Aleuron. For the precise distinctions which obtain between Enyo
and Aleuron I must refer my readers to the figures, no written descriptions
having been made at the time. The great difference between the green and
maroon forms rather led me to anticipate a distinct species on the second occasion.
336. Enyo pronoe pronoe.
R. & J. p. 400.
This is the one and only species of Sphingidae, so far as I am aware, which
has been recorded for Para by others but has evaded both myself and my one
enthusiastic colleague who takes any interest in the study. Unless I have mixed
up my earlier specimens, now in England, with japix, I have not seen the moth,
and can do nothing more than refer to the note in the Revision, p. 401.
337. Epistor lugubris lugubris. (Plates 7 & 10.)
R. & J. p. 403,
26
398 NOTITATES ZOOLOGICAE XXVII. 1920.
338. Epistor ocypete. (Plates 7 & 10.)
R. & J. p. 405.
Both exceedingly common at light in Para, especially the former. I take
these two species together for the convenience of description, and because,
though undoubtedly distinct, their larvae are at times almost impossible to
differentiate. With an increasing acquaintance of them both, I find it less easy,
strange to say, than I once thought, to point to their essential differences, due
mainly to the fact that both have a large range of variety in colour and markings.
They are practically of the same size ; both have straight, thick, leaden-
coloured horns, enclosed dorsal areas, and 8 or 9 oblique side-stripes directed
tailwards ; both assume various greens and pinks as a ground-colour, and both
feed on various species of Cissus (Vitaceae). The word Citrus on p. 402 of the
Revision is unquestionably a slip or a misprint for Cissus, for surely no one is
going to be audacious enough to suggest that an Epistor ever sank so low as to
leave the juice of the grape and suck an orange !
On the other hand, ocypete forms an interesting connecting-link with the
two former genera by its fondness for Davilla rugosa {Dill.), on which it is much
more frequently found. I think also that I am right in saying that ocypete is
rougher in surface, more besprinkled with white or yellow dots, and that its
dorsal and lateral stripes are more clearly white and more strongly defined with
a deeper tone of the prevailing colour of the individual specimen, be it blue-green,
yellow-green, or a shade of carmine red. Both species have yellow-green forms
bearing a mesial and a double lateral series of more or less prominent red patches
evenly situated on all their segments, and reminding one much of the variation
so commonly seen in the European Smerinthus populi. In the early stages
lugubris is often thus or entirely pink, and generally changes later to blue-green,
especially when feeding on the similarly-coloured leaves of Cissus sicyoides,
known locally as " carao " or " pareira braba." On another species of Cisstis,
known as " cipo puca," it is sometimes irregularly marked with red-brown on
a warm green ground, and once or twice I have taken it as if splashed with black
ink or tar.
The larvae of both species are hardy and voracious feeders, and produce
an unusually large quantity of moderate-sized and rather round moist green
excrement. But few parasites have as yet been noted in association with this
genus, but I once bred a single large black wasp from a larva of ocypete.
The pupae are plain brown and gloss}', with long sharp cremasters and a
microscopic amount of bifurcation at their tips. They are formed a little below
the surface of the earth without much admixture of silk.
Length of proboscis an inch or less.
339. Epistor gorgon. (Plate 7.)
R. & J. p. 405.
Though occasionally taken at light, this is much rarer than the two former
species in Para. The disparity in shape and colour between the two sexes of
the moth is a strange and misleading feature to the uninitiated. Twice only
have I bred the species from larvae found feeding on Cissus sicyoides. This is
like lugubris in colour and design, but the horn is dark brown and definitely
NOVITATES ZOOLOGICAE XXVII. 1920. 399
curved, and the same brown colour not only borders the anal segment but bisects
the anal flap. The thoracic segments, too, are more puffed out laterally.
Pupa like the foregoing but bigger, with a very long pointed cremaster a
slight degree more forked.
340. Epistor taedium australis.
R. & J. p. 406.
Of this species I can say no more than that a single male moth was taken
at a Para electric lamp early in 1918, and was thought to be only a small dark
specimen of gorgon. By comparison later, however, I became convinced that
it was distinct. I submitted it to Mr. Preston Clark, of Boston, who declares
it to be a male of taedium australis. It is doubtless a rare species here, and almost
certain to be another Cissus feeder.
341. Epistor cavifer. (Plate 10.)
R. & J. p. 407.
From a single moderate-sized green egg found in January 1919 on Cissus
sicyoides in Utinga (the Para water-works territory), I reared a small green
Sphingid larva. This seemed so like many others that, up to the final instar,
I did not figure it, anticipating only gorgon which I had already drawn and
painted. At this stage, however, it appeared so much more elegant and in-
teresting that I began to entertain hopes in regard to one or other of the rarer
kindred species, and decided that at least it merited a second portrait. It
then formed a typical Epistor pupa like gorgon with a long sharp cremaster, and
justified my hopes on February 18th by emerging into a perfect male of cavifer,
a species which I had never hitherto met with in Para. Curiously enough,
during the latter part of March I secured four more young larvae of this species,
feeding on a large vine-like form of Cissus in the Para " Bosque," all of which
attained full growth. Then one unaccountably succumbed to some prevailing
larval epidemic, while the remaining three pupated satisfactorily, as I thought.
Even one of these, however, was doomed, for a week or so later it lay limp and
motionless with the abdominal segments distended, and then through a small
dorsal aperture in the thorax there appeared the unholy dark form of a dipterous
cocoon.
From the second or third instar these larvae were very distinct from lugubris
and ocypete, and shared the characters of gorgon, viz. more swollen thoracic
segments, irregularly edged on approaching the ventral area with dark brown.
Furthermore, the anal segment was ringed and the flap bisected with this same
colour, and the horn, especially in the last instar, was a perfect hoop, very long,
immensely curved, and of a dead sepia tone. It may be mentioned here that
this somewhat striking and unusual ornamentation of the anal segment, apart
from the horn, which is so pronounced a feature in cavifer and gorgon, is not
infrequently, but only vaguely, foreshadowed in pink in lugubris and ocypete
in those yellow-green forms possessing a strong consecutive series of pink spots.
At this stage also the spiracular area, especially on segments 6 to 10 inclusive,
is beautifully adorned with a nondescript light brown design on a delicate apple-
green ground ; and though the oblique side-stripes lead up to the horn, they are
bowed and not strongly delineated, while the dorsal area is inversely marked
400 Novitates Zoolooicae XXVII. 1920.
with a series of V's pointing headwards. I find now that I figured this larva
from a specimen taken in the Interior of Peru in 1909, but as I failed to rear
the moth the figure remained unidentified and consequently unpublished. I
have never consciously seen the moth at light, and can only regard it as a rare
species hereabouts.
353. Nyceryx coffeae.
R. & J. p. 417.
A single and very perfect specimen of a beautiful Hawk-moth, quite new
to my eye, has suddenly turned up in Para. I took it from the wire of a bright
electric arc globe opposite my house at midnight on May 25, 1919.
365. Perigonia pallida.
R. & J. p. 425.
Fairly common as a moth at light in Para.
Larva probably a Rubiaceous feeder, but all efforts to trace its early stages
have so far failed.
367. Perigonia lusca f. restituta. (Plate 7.)
R. & J. p. 426.
Generally common at light in Para, and often found burnt in the debris
from broken arc globes.
Larva uniformly cylindrical, plain apple-green or white-green, with very
narrow white mesial stripe. The head is blue-green and the horn only slightly
curved. The last of the 7 light oblique side-stripes leading to the horn is, as
in the case of so many species, though not in the genus Epistor, heavily edged
with dark green above and sometimes touched with black. This and the suc-
ceeding species of Eupyrrhoglossum and Sesia share a feature in common which
is calculated to terrify away intruders. I refer to a certain strained attitude
sometimes adopted, these larvae when disturbed throwing their heads back
and exhibiting large lunules of velvety black in cadmium or lemon-yellow settings
on the ventral area of the second and third thoracic or leg segments. At all
other times these markings are completely hidden. The larva of lusca feeds
sometimes on Ourouparia guianensis, but more often on the leaves of two species
of coffee, Coffea arabica and liberica, all Rubiaceous plants.
The pupa differs but little from Epistor in appearance, or in the position
chosen for its formation.
371. Eupyrrhoglossum sagra. (Plate 9.)
R. & J. p. 430.
A rare moth in Para, though apparently a common species elsewhere, with
a very wide range of distribution. Until lately I had never taken the species
here, and recorded it simply on the authority of two friends, Mr. F. Ducke of
the Para Museum, who captured a specimen at Pinheiro, 10 miles down the
river ; and Mr. T. T. Dyer, who took another in good condition at a lamp in
the city on March 5, 1919.
On April 21, however, I had the good fortune to procure a single larva
Novitates Zoological XXVTl. 1920. 401
of this species feeding on Sabicea aspera (Rubiaceae), or, to be more accurate,
preparing for its penultimate moult on the underside of a Miconia leaf, which
was obviously not its food-plant. This produced a perfect moth on May 12,
1919. On the completion of its ecdysis, I found that this was another species
which I had figured in Peru, but that as it subsequently died it remained un-
identified. I have made two new figures, and am now practically certain that
yet a third Peruvian illustration of a larva with the same general bearings, but
green and stouter, can only be referred to that of its congener, E. corvus. This
latter species, however, is not a native of Para, and the figure remains unpublished.
The larva of sagra in the fourth instar is of a warm brown, with the customary
7 dark oblique side-stripes and 4 light red patches below these stripes on segments
8, 9, 10, and 11. The horn is much erected, curved back, and then turned up.
In both this and the final instar it is extremely rough and file-like on the upper
edge, and disproportionately so about the middle of the lower edge, terminating
in a sharp black spike. In both also segment 2 is pointed, and forms a cowl
for the head. The chief differences in the last stage are as follows : colour
intensified to brown madder, dorsal area light pink, latter portion of mesial
stripe deep maroon, light bordered and broadened about the centre ; bent stripe
on thoracic segments and a distinct mesial line marking the ventral area ; patches
of colour on segments 8-11 now emerald-green and white, suggesting the figure 5
four times repeated, one green spot on 7 and a patch of green dots at a higher
elevation below the stripe on 12 ; spiracles light red ; legs ochreous, on segments
3 and 4 springing from yellow-ringed black patches ; a dark tract behind horn
to anal flap ; horn very rough as before on upper and lower edges, but black
spike now down-turned ; the whole larval area besprinkled with minute light
dots. Excrement dark brown, roundish, and the segmental divisions much
obliterated. In so many ways does this species show its obvious kinship with
Sesia that, were it not for certain anatomical considerations in the moth, deemed
important by the expert, the clumsy word Eupyrrhoglossum might well be
eliminated, and its couple of species included in that genus.
373. Sesia ceculus. (Plate 7.)
R. & J. p. 433.
A common species about Para, as elsewhere, but only rarely drawn to light,
and more often seen, like the Humming Bird moth of Europe, flying over grass
and flowers along roads and railway cuttings, and generally late in the afternoon.
Two forms of the larva have frequently been met with, and so different are they
in colour and markings, and so constant is this difference in direct association
with food-plant, that for long I was almost convinced that they represented
two species. But the resulting moths are identical in all respects, and I have
now come to the conclusion that this is only a parallel case with that of P. strigilis,
for example, and that neither of them admit of any specific subdivision. The
difference in the colour-scheme and pattern of their larvae in these cases would
appear to be purely a matter of environment, depending wholly upon the favoured
food-plant, and by superficial resemblance conferring upon them a temporary
protective benefit. The two plants chosen by ceculus in Para, though very
different from one another, are both Rubiaceous creepers, Ourouparia guianensis
and Sabicea aspera.
402 Novitates Zoolooicae XXVII. 1920.
Both larvae are green, but the form found on Ourouparia is bluer, always
inclines to white on the dorsal area, and never has more than the normal 7 oblique
side-stripes, the first and the seventh being far more pronounced in white than
the rest. The commoner variety, however, which is equally constant when
found on Sabicea, though varying in the intensity of the side-stripes, now light
red or maroon in colour, has always an extra bent stripe on the thoracic segments,
and often the commencement of a posterior stripe just in front of the last spiracle.
In this case the first and seventh stripes are hardly more prominent than the
others, though the seventh always connects with the medio-dorsal line, and is
sometimes supported beneath by lemon-yellow. The anal flap is, as in so many
of the allied species, marked with a red-brown passage proceeding from the
base of the horn.
The puparium is formed just below the surface of the earth with a modicum
of silk uniting dead leaves, etc., and the pupa is shorter and more dumpy than
those of Epistor and Perigonia.
Length of proboscis in male moth J in.
376. Sesia titan. (Plate 7.)
R. & J. p. 436.
377. Sesia fadus. (Plate 7.)
E. & J. p. 437.
We come now to the last two species of the subfamily Sesiinae, which, with
its 47 species or more, out of a total of not much over 120 for the world, is indeed
strongly represented in Para.
Though it was long before I saw either titan or jadus at all, and have but
seldom since taken the moths at light or observed them during the day, my
experience of a few years in the place proves that both species may be reckoned
fairly common here, and that they constitute but one instance out of a number
in Sphingidae where two or more species are so closely related as to be easily
confused, but where, nevertheless, there is no question about their specific dis-
tinction. I deal with them together to facilitate comparison.
Once again the importance of the study of the early stages is emphasized,
and having now been fortunate enough to work out the secrets of their life-
histories, I find both species to be associated with Rubiaceae and locally plentiful
in the larval condition, titan feeding on Randia formosa ("acucena"), and very
occasionally upon Genipa americana (" genipapeiro "), while jadus is invariably
found on the fresh leaves of the saplings of this latter tree. In both cases it is
not uncommon to find three or four ova and several young larvae on the same
plant, but if left too long they generally disappear, and are probably consumed
by lizards. Such has too often been my experience when, for the betterment
of their growth, I have trusted young larvae to nature, unprotected from its
decimating forces.
The larvae of both these species are of a plain apple-green colour, finely
sprinkled with white dots, possessing the usual 7 oblique side-stripes, the first
and seventh being the whitest and most pronounced, and the seventh containing
a greater or less degree of pure pink and a touch of lemon. The mesial line is
dull green and terminates with a stout, curved, and leaden-grey horn. The
NOVITATES ZOOLOOICAE XXVII. 1920. 403
second and third pairs of legs in both species, as with ceculus, E. sagra, and
P. lusca, spring from large black lunules set in cadmium or lemon-yellow.
A handsomely variegated larva in brown with yellow side-patches, recalling
the normal form of E. sagra, but with the first and seventh stripes alone clearly
defined in cream-white and edged above with black, once occurred on Randia.
It produced on emergence, as I had anticipated, a typical specimen of titan.
The pupae, like ceculus and E. sagra, are dumpy, of a plain glossy brown,
and with sharply-pointed cremasters. Though the moths are now sufficiently
well known, I am bound to confess that in their larval and pupal conditions,
apart from the considerations of pabula, etc., they appear to offer but few
differentiating features sufficiently constant to enable one to say with absolute
certainty which is which.
Subfamily PHILAMPELINAE.
This fourth subfamily is, so far as I can ascertain, represented in Para by
but the one genus Pholus, but of the 19 species that are known, we can at any
rate boast of possessing 9. Of these the larvae of 5 feed on Vitaceae, Vitis,
Cissus, etc. ; 2 on Onagraceae, various species of Jussieua ; and 2 remain alto-
gether unknown as regards their food-plants and early stages. Those larvae
that are green invariably ripen to a deep red on their dorsal areas at full growth,
wander some distance away from the region of their excrement, and form their
large puparia well underground without any apparent admixture of silk. As
with most Sphingidae in these parts, the moths generally appear in less than a
month. The eggs are usually to be found deposited singly on the under-surface
of the freshest leaves.
408. Pholus anchemolus. (Plates T.Z.S. & 9.)
R. & J. p. 478.
One of the commonest of the genus, both sexes frequently occurring through-
out the year in Para at the city arc lamps.
The immense plain green larva has a graduated series of broad oblique
side-stripes, enclosing the spiracles and directed headwards. These, in increasing
ratio, are situated on segments 9, 10, and 11, and are always of a clear lemon-
yellow, not white, as stated in the Revision. Spots of irregular size and shape
but of the same colour mark the sides of some or all of the four anterior segments.
A deep vinous-coloured form with precisely the same markings is also taken
here, but less commonly. It is to be found on Cissus sicyoides, erosus, etc.,
growing over palings or festooning trees in the shade, and up to the present
in my experience it enjoys the happy reputation of being immune from parasitic
attack. The pupa is of great length, of a dark red-brown colour, more glossy
than fascialus but duller than vitis, and is possessed of a long, stout, and well-
curved cremaster.
Length of proboscis in both sexes 2\ in.
410. Pholus satellitia licaon.
R. & J. p. 480.
The Revision records a specimen of this subspecies taken by Dr. Goeldi at
electric light in Para in March, some time before the year 1903, when everything
404 Novitates Zoolooicae XXVII. 1920.
apparently was vastly more plentiful than it is to-day. I had almost begun
to doubt the existence of satellitia here, but while I was away in Pernambuco
during April and May 1918, my friend T. T. Dyer, without knowing it, took a larva
on Cissu-s, from which he bred a perfect female of this moth, bearing considerable
resemblance to a large eacus. I recognized the difference on my return, but as
he had not anticipated anything new or exceptional, he could tell me nothing
about the form or colour of the caterpillar. I have since taken a perfect male
at light.
The record is useful in proving that this species, with its immense range
of distribution from Canada to Argentina, and apparently common in some of
its subspecific forms in other places, is still alive here though unaccountably
rare.
415. Pholus obliquus.
R. & J. p. 486.
Moth in both sexes fairly common at light in Para and often in perfect
condition. Examination of the abdominal contents of the females of both this
species and anchemolus has on occasion revealed strings of small and immature
green ova, indicating that some time would have to elapse, and that probably
some feeding on the part of the moth would have to take place before oviposition
were possible. All my attempts to get a picture of the larva of obliquus have
so far disappointingly failed. During my absence in Pernambuco, as with the
previous species, my friend T. T. Dyer had another piece of exceptional luck
by finding one in the shade of the Utinga matto. It was nearing full growth
and feeding on the common Cissus sicyoides, consuming also the flat, trunk-
clinging leaves of some Epiphite, a seemingly strange departure. He was unable
to figure it, but described it as a very large and handsome caterpillar in two
shades of red-brown without stripes but with a series of lighter lateral markings.
After breeding a perfect female moth of obliquus, which he did simultaneously
with my return, he kindly gave me the empty pupa-shell. This I may describe
as practically identical in form and colour with anchemolus, and differing only
in the cremaster, which is distinctly less curved, appears even stouter, and
terminates with a minute but obvious fork. Though obliquus is undoubtedly
a much rarer species than anchemolus, and recently (1919) has not been observed
at all, that so many great larvae, especially of a species like this where the food-
plant is known, should manage so skilfully to keep out of sight, is a problem which
I can only explain on the supposition that they live high up in the trees or in
the denser and more inaccessible parts of the forest.
416. Pholus eacus. (Plate 9.)
R. & J. p. 487.
A perfect female moth was taken at light in Para on May 21, 1912, and the
species lost sight of till February 1916, when I discovered a full-grown larva
upon an arborescent species of Jussieua (Onagraceae), probably suffruticosa or
salicifolia, growing in a ditch.
This was of a plain light green with 6 broad oblique side-stripes in pale
yellow, faintly margined above with red, and directed headwards. At the time
I took it for an extra large specimen of the green variety of fasciatus, the form
Novitates Zoological XXVII. 1920. 405
which so frequently occurs in Para on the same and kindred plants, and I kept
it simply on account of its size. It then turned red, and formed a pupa more
like that of anchemolus ; but being busy at the time, and not anticipating anything
new, it was only on the emergence of a lovely female moth of eacus on the evening
of April 30 that I realized how faulty had been my observations, and how nearly
I had lost a prize. Since those days eacus has been a fairly common species to
me, for though but two or three specimens of the moth have been taken at light,
many have been bred.
While I was at Iquitos in February 1917 my devoted and sharp-witted cook
found me about 16 ova and larvae, and I have generally been able to procure
more by returning to the same place at the same time and during the three
succeeding months. This favoured locality is known as Entroncamento on the
railway-line, 11 kilometres out of the city, and here this particular species of
Jussieua grows to quite a respectable small tree in the ditches, and thrives on
a tract of wet white sand. Unlike its less fastidious congener fasciatus, eacus
in nature appears to be restricted to this species, and does not do well in captivity
when only provided with other more readily obtained varieties of Jussieua.
It has occurred in two other localities, but always on the same plant. The
larva of eacus is as constant as fasciatus is variable, and is always green with
only 6 light stripes which are bordered above with red. Its egg, though much
smaller than that of anchemolus or labruscae, is nearly twice the size of fasciatus,
and rather whiter. . -
With a little experience one is able to pronounce with certainty upon the
difference between eacus and the green form of fasciatus ; but the general likeness
between their larvae as Jussieua feeders would seem to indicate that eacus is
out of place, and that in reality the two species are more closely related to one
another than fasciatus is to vitis, with which it was once so erroneously confounded.
Though kept from the light, this moth tends to fade more than many others
Length of proboscis in female moth If- in.
422. Pholus vitis vitis. (Plates T.Z.S. & 10.)
R. & J. p. 491.
In regard to this already described and well-known species, I need say but
little. Merely have I to record that the moth, though occasionally observed at
electric lamps in Para, and perhaps a trifle larger and brighter than those which
I used to breed from the vines of Lima, is here comparatively rare. Our climate
is too hot and wet for the vine to flourish, and I cannot remember to have taken
the larva on more than six or eight occasions when searching for other larvae
on Cissus.
423. Pholus fasciatus. (Plate T.Z.S. & 2.)
R. & J. p. 494.
This species, too, may be dismissed with a short paragraph, as it is now so
well known. The moth is very common at light in Para.
Several species of Jussieua, the natural food-plants, grow abundantly in
ditches and in other wet places throughout the district, and it would appear
that the larva of fasciatus is at all times and in all places to be found associated
therewith. Among the many-coloured varieties of the larva already figured,
406 Novitates Zoologicae XXVII. 1920.
the green form with its 8 clearly-defined oblique side-stripes, comparatively rare
about Lima, is here undoubtedly the prevailing form. No shade of difference
can, of course, be detected in the moths, and I assume that this is but another
nice adaptation to a greener and more flourishing vegetation. The egg of
fasciatus is not only much the smallest of all the species of Pholus with which
I am acquainted, but is probably one of the smallest of all Sphingidae, when
considered in relation to the weight and bulk of the full-grown caterpillar or
the size of its moth. The little light oval green egg and the tiny milk-white
larva with its erect black tail which hatches from it are very similar to those
of Sesia ceculus, and if anything a trifle smaller.
The pupa, which occasionally produces a big dipterous parasitic fly whose
presence cannot always be detected in the larval condition, differs from all the
other species of Pholus dealt with in being dead black in surface, relieved by
brown in the interstices of the abdominal segments, and the cremaster is short
and slender by comparison.
Length of proboscis in male nearly 2 in.
424. Pholus phorbas.
R. & J. p. 495.
425. Pholus capronnieri.
R. & J. p. 496.
These two beautiful species are not infrequently drawn to the electric arc
lamps of Para, the males and females of both occurring in perfect condition,
and being picked up on the pavement together with hosts of other commoner
moths. Times, however, have changed for the worse, and they have hardly
been seen since 1917.
Though I have not even yet abandoned the hope of some day finding their
larvae, I have already searched hard, but with no result beyond the growing
conviction that neither of them is associated with Vitaceae or Onagraceae.
426. Pholus labruscae. (Plate T.Z.S.)
R. & J. p. 496.
A fairly common species as a moth at light in Para, and the larva frequently
taken on the various local forms of Cissus (Vit.), and once on a vine-like creeper
in the Botanic Gardens, Siphania glaziovee (Menespermaceae), introduced from
the Upper Amazon.
My experience is that of others when I say that it is next to impossible
in this hot and humid climate to prevent this lovely green moth from fading
and contracting bleached or ochreous patches on wings and abdomen. I
have little new to add to my notes and illustrations of the species made in Peru,
and to the ample descriptions of its larva and pupa given on p. 497 of the Revision,
beyond pointing once again to the marked difference which labruscae shows
from all other known species of Pholus both in the larva and pupa, the latter
being possessed of a very broad, rough, and flattened cremaster.
Length of proboscis in female moth 2i in., in male 2J in.
Size of excrement from full-grown larva $ x | in.
Outwardly labruscae would appear to merit a separate generic status every
Novitates Zoolooioae XXVII. 1920. 407
bit as much as Amphimoea walkeri or Pseudosphinx ietrio, and even more, I
venture to think, than Eupyrrhoglossurn sagra ; but from the point of view of one
who is chiefly interested in co-ordinating an array of facts relating to early stages,
and forming some rough estimation upon the degree of kinship between related
species, the creation of new genera is a nuisance. Unless some nice point, some
subtlety of scientific import in regard to generic distinction, has passed me
by unnoted and unappreciated, it seems to me that the association of as many
species as possible in a single genus, with here and there a slight readjustment
in their sequential order or grouping, would be far more instructive than the
mere multiplication of genera — an opposite process which seeks rather to
emphasize differences of outstanding importance, but which, with our still very
limited knowledge, is bound to be somewhat arbitrary and lacking in finality.
If it be conceded that the grouping of more species in fewer genera would
aid the collector in the field, it naturally follows that greater benefit would
accrue to the museum student, who always wants the fullest material possible
for purposes of comparison.
Subfamily CHOEROCAMPINAE.
This fifth and last subfamily of the Sphingidae is in Para limited to the
one exclusively American genus Xylophanes ; but as its local representation
out of the 50 to 60 species known already amounts to a dozen species, one being
quite new and others esteemed as rarities, the interest attaching to it is well
sustained.
The larvae of seven species have been discovered, bred, and carefully figured
in their various stages, and the remainder, as yet undiscovered, cannot be far
away. It is noticeable that all but one are Rubiaceous feeders, and the inference
that Xylophanes, as a compact genus, is in its entirety more or less restricted
to Rubiaceae, should, if correct, materially aid the investigator of early stages
by eliminating the more unlikely forms of plant-life. Most of the larvae are
snake-like and secretive in habits, and some are much troubled by parasitic
attack. The excrement bears specific peculiarities ; in chiron alone, of the species
dealt with, being of the normal hexagonal and tripartite form. In the others
it is almost or entirely devoid of this pattern and exceptionally large, while in
species like mossi, guianensis, and amibus it is of phenomenal size, dark brown
or blue-black in colour, and either rounded or of an irregular elongate formation.
These larvae, like so many others, tone to a redder hue and lave their bodies
with a frothy substance from the mouth prior to leaving the plant for pupation.
In this palpably sticky condition they appear nearly always to wander some
distance away from where they have been feeding, and spin a glutinous web
amongst vegetation and dead leaves on the surface of the earth to form their
puparia.
Though the pupa of each species differs in the precise shape and form of
the cremaster, and to a slight extent in tone of colour, a general type is adopted
throughout, which may roughly be described as bone-coloured with a mesial
dark line, more or less pronounced and continuous, marking both the dorsal
and ventral areas. The region of the spiracles, themselves brick-red, is heavily
spotted with black, and the entire surface is minutely freckled with light-brown
or olive-green marks.
408 NOVITATES ZOOLOQICAE XXVII. 1920.
631. Xylophanes pluto.
R. & J. p. 681.
Of this widely distributed and common species, with which I became
acquainted some years ago in the Interior of Peru, I have here but to record the
capture of a single perfect male at a Para lamp near the end of March 1919.
This was taken by Mr. T. T. Dyer, who is confident that he there and then missed
another example of the same species, which was very strange, for its observed
occurrence in this particular part of S. America is, so far as I know, without
precedent.
In regard to Erythroxylon, its reputed food-plant, E. coca, which is so
extensively grown as a drug in other parts, is in Para a comparatively rare plant
in gardens, and I have never found it touched by anything beyond a small
Geometrid larva. The larva of X. pluto may subsist on other plants, but in
any case it must be a very rare species hereabouts.
Xylophanes mossi. (Plates 5 & 8.)
Xylophanes mossi Clark (1919).
In his paper on " New Sphingidae," published in the Proceedings of the
New England Zoological Club, my generous friend B. Preston Clark has described
this species, and been pleased to attach my name to it as its original discoverer.
Strange to say, I have never yet taken it wild in the imaginal condition, but
since 1914, when I found my first larva and some eggs, I have repeatedly bred
the species. No definite months can be given, as I have taken or observed signs
of the larva at almost all times of year, and too' often have I had the mortification
of being just a few days too late, finding the plant vigorously eaten and some
enormous pellets of fresh excrement lying on the ground, but the larva gone.
Even when it has been found, I have by no means always met with success,
as the species is so ravaged by parasites ; and I think I am fairly stating the
case, when I say that I have bred from 15 to 20 perfect males and females out
of some 60 larvae in 6 years, and just managed to miss about twice that number.
The plant on which the larva feeds, Pagamea guianensis (Loganiaceae, or Rnbiaceae
according to Dr. Huber), is distinctly local, being restricted to the particular
type of sandy soil found between Souza and Tapana on the Pinheiro railway-
line, but significantly absent from the adjacent Utinga water-works region. It
is also fairly abundant in the Isle of Mosqueiro, and in all places where the plant
grows I have traced the larva. As these localities range roughly from 10 to 25
kilometres from our city station, the distance may possibly account for the
non-appearance of this moth at light. I say this advisedly, for though the
Sphingidae as a family are known to be long and strong fliers, and it is beyond
question that many species are thus drawn from very considerable distances,
there is as yet no proof that all Hawk-moths wander far from home. And
furthermore, if this be the case, it is more than probable that in the vast reaches
of the tropics of this continent there are links in the Sphingid chain of life still
extant, and many another species yet waiting to be revealed to science. I
have already given a general description of the larva on p. 349 of the general
introduction, and need only add the following : The small, down- turned tail
of the adult larva is a most peculiar feature, differing from all other known species
NOVITATES ZOOLOGICAE XXVII. 1920. 409
of Xylophanes ; the head is small and typical of the genus ; the tapering anterior
segments by no means reach their maximum with the ocelli on the 5th segment,
as is so often the case, but only with segment 12 which appears enormously
swollen ; and, finally, this stout caterpillar, whether it be of the normal pink
and burnt sienna coloration with its 5 viridian-green side-patches or green-grey
with 7 lemon-yellow side-stripes, is distinctly Pholus-\ike in appearance. The
frass is enormous, blackish brown, rounded or of regular oval form, and tightly
packed in thin successive layers. Seldom are more than 8 pellets dropped in
the 24 hours. The growth is, nevertheless, extremely rapid, the last instar
never exceeding 5 days, and the whole larval period being generally under 20.
The pupa is typical of Xylophanes but rather redder than most, and it is possessed
of a long, blade- like cremaster.
In regard to the parasitic attack to which this species is so lamentably prone,
I have five observations to make :
( 1 ) The egg is sometimes stung by a minute hymenopterous fly.
(2) A dipterous fly stings the young larva while it is still small, generally
in the second or third instar, I believe.
(3) Neither then nor in the succeeding instars is there any apparent sign
of the presence of the foe within, no lack of vitality observable in the larva, no
irregular feeding, and no protracted growth, as is often the case, and nothing
irregular in its colour or in the nature of its excrement.
(4) After spinning its puparium the larva invariably, whether healthy or
otherwise, produces an abundance of brown slime in which it lies. When it is
stung, however, it begins to look limp, and exhibits irregular brown stains on
the second day.
(5) The larva is just alive on the third day and capable of feeble movement,
but the dipterous maggots, in this case generally less than 10 in number from
any individual, emerge from the body of the host to form their own cocoons
separately in the soil. This occurs invariably on the evening of the third day,
and precisely at the time when the larva, had it been healthy, would have cast
its final skin and become a pupa. Repeated instances confirm these observations
in every detail, and the accuracy with which the whole process is timed is little
short of marvellous. Many Sphingid larvae, as already stated, lave their bodies
with a sticky substance prior to pupation, and other species of Xylophanes make
what we should call a mess of their puparia, but none, so far as I am aware, to
a like extent. What particular purpose the froth or slime serves is not apparent ;
it may be to assist ecdysis, or it may be to prevent the intrusion of small forms
of creeping life at a period when both larval and pupal skins are peculiarly
sensitive and liable to damage.
638. Xylophanes porcus continentalis. (Plate 8.)
R. & J. p. 685.
Dating back to March 1912 when I found my first larva, and to the next
three years during which I secured but half a dozen more, I esteemed the species
rare in Para. Since then, however, though only one moth of porcus has been
recorded at light, I have so repeatedly taken its egg and the young or full-grown
larva on fresh saplings of Palicourea grayidifolia (Bubiaceae) in such localities
410 NOVITATES ZOOLOGICAE XXVII. 1920.
as Utinga, where this plant thrives in abundance, that I regard it now as almost
the easiest species of the genus to obtain hereabouts.
Its food-plant is of wide but not universal distribution, growing in the
shaded matto on the north a«d eastern outskirts of the city, but being apparently
absent in the muddy region which borders the Rio Guama. The eggs of porcus
are generally deposited singly upon the upper side of the tenderest yellow-green
leaves of the plant, and throughout its growth the larva is to be found on the
under-surface of half-consunied leaves, clinging firmly to the mid-rib, never
on the stems or the earth. It is always of a pure apple-green colour, with small
light caerulean blue ocelli on segment 5, and 7 yellow side-stripes leading up
to the horn, which is plain pink, smooth, and well curved.
The pupa is typical of Xylophanes, though somewhat more olive-green in
tone, heavily lined with brown, and possesses a shorter but broader blade-like
cremaster than the foregoing species.
Length of proboscis in female moth 1|- in., in male 1 in.
651. Xylophanes guianensis. (Plates 5 & 8.)
K. & J. p. 692.
This species, like the former, has, strange to say, only once been observed
as a moth at light in Para, but from the numerous occasions in at least seven
different months when I have taken the larva on Palicourea grandifolia
(Rubiaceae), or the egg, readily detected on the upper- or under-surface of its
large, flat leaves, I am bound to regard it as by no means rare here. The larva
up to the end of the fourth instar is long and thin, and being of the same colour
as the upper surface of the leaf, a sage- or blue-green, it always reposes during
the day in that position along the mid-rib and is easily passed over. At this
period the dorsal area is enclosed by a couple of yellow longitudinal stripes,
terminating in a straight, recumbent horn, adorned with small black tubercles.
In the last stage the enormously long pellets of blue-black frass beneath
the tree frequently betoken its presence, but now having assumed a very dark
vinous-brown colour, the larva is only to be found on the trunk, generally at
the base in heavy shade, or even several feet away from it, resting on a stick
or on the soil among dead leaves. The eye readily detects its characteristic bite,
especially when the tree is small and the leaves very large and not too
numerous.
From Mr. Schaus's description of the larva of ceratomoides, its next-of-kin,
it would appear that guianensis corresponds pretty closely. A plain ochreous
spot or two represents the ocellus on segment 5, and it possesses a long, stout,
and perfectly straight blade-like horn, which is saw-edged above and below,
and terminates in a spike.
The cremaster of the pupa is similarly large, flat, and broad, and spiked
along its angled extremity.
The species is sometimes troubled by dipterous parasites.
Length of proboscis in male 1J in.
652. Xylophanes anubus. (Plate 8.)
R. & J. p. 693.
Quite a common species in Para, as elsewhere, judging from one's success
with its larva, but once again, like the three former species, very seldom is it
NOVITATES ZOOLOGICAE XXVII. 1920. 411
drawn to light here. Indeed, throughout my time in Para I have only twice
come across the moth, one being taken in a strong cobweb, and the other, a female
in almost perfect condition and of a peculiar chestnut colour, especially in the
hindwings, being picked up dead in the Port of Para Buildings in May 1915.
So different did this appear from all my bred examples, which are umbrous
inclining to olive, that, until Dr. Jordan had examined it, I was of opinion that
it was something distinct. I may here add that this suffusion of a delicate
olive-green in all my Para-bred specimens was never noted in those caught in
Peru, which always seemed browner and more heavily lined.
The larva here feeds on a couple of species of Palicourea (Rubiaceae) with
dark glossy leaves, the bigger of the two growing in dry and open parts where
the forest has been cut down, the other, a more slender plant, being invariably
associated with the sides of streams and boggy ground. Up to the end of the
fourth instar the larva is of a pallid and subdued green, like the under-surface
of the leaves referred to, and where during the day it constantly remains. The
fifth segment is now considerably swollen, and its ocellus at this period is large
and striking, a finely pencilled black ring containing a patch of lilac and an arc
of pure light blue in front. Its tail, once long and drooped, is now and up to
the end of its larval stage an ample and well-curved horn. In the last stage,
like guianensis, antibus is brown, and invariably remains during the heat and
brilliance of the day on the brown stems in the shade near the ground, or more
often actually on the ground beneath dead leaves. The ocelli, which are now
black in fine blue rings, are proportionately reduced, the dorsal area is enclosed
by rufous and dark lines from head to horn, and the side-stripes are represented
by 7 rather obscure and waved lines in moss-green directed tailwards. At this
stage I have very frequently taken it, once the secret of its whereabouts was
disclosed, but, as with mossi and guianensis, I suppose I have equally often been
just too late, and experienced the keen disappointment of finding only stripped
branches and an abundance of fresh frass. This again is enormous, but of
umber or dark brown compared with that of the preceding species.
Though I have often pulled up everything alive or dead for yards around,
and raked the ground till I have dripped with perspiration, I have never been
able to trace this or any other species of Xylophanes but tersa to its puparium
in nature.
The pupa is lighter and more slender than guianensis, with a blacker medio-
dorsal line and a much finer cremaster.
The species is occasionally troubled by diptera, and I once bred a single
blue- black wasp from a large white hymenopterous grub which emerged in the
puparium from the body of a dying caterpillar.
Length of proboscis in male moth If in.
654. Xylophanes amadis goeldii.
R. & J. p. 694.
In this little-known form of amadis, Para exhibits one of the prizes of its
rich and variegated fauna. In the Revision there is but one record of a female
having been taken at electric light in Para during the month of May by Dr.
Goeldi, and sent to the Bern Museum. In July and August 1912 I had the good
fortune to take three males here in the same way. My next find was that of a
412 Novitates Zoolooicae XXVTI. 1920.
perfect female on a lamp in front of the Museu Goeldi in December 1916, and
this I sent to Mr. Preston Clark, together with a male caught by Mr. Dyer
in 1918. I then missed a male which had perched up at the top of a high lamp-
post in January 1919, and my friend did the same towards the end of May. On
March 28th of this year, however, I managed to secure another freshly-emerged
female in very perfect condition on a lamp almost opposite my house in the
Largo de Baptista Campos. In stuffing her long and narrow abdomen with
wool, as a precautionary measure, I extracted 78 green eggs of moderate size.
Diligent examination, oft repeated, of the Rubiaceous plants favoured by amibus
and others, has so far completely failed to reveal the larva of this elegant species,
which, although rare, is, from the above records, obviously well established in
Para, and would very likely be found to exist here in some numbers, could one
but unravel the secrets of the early stages of its life.
Length of proboscis in female moth 2 in.
655. Xylophanes epaphus.
R. & J. p. 696.
My general remarks on the previous species apply equally here, no larva
or knowledge of food-plant or early stages having rewarded the repeated
examination of all likely plants in the Order Rubiaceae. To know the habits
of epaphus would be to discover a veritable gold-mine, for its food-plant is hardly
likely to be anything more pretentious than some humble ground-weed like
Spermacoce or Psychotria, growing in some particular shaded or even wet locality,
and the find of a single caterpillar would almost certainly lead to the discovery
not only of amadis but of kindred species like docilis and cosmius in their
respective regions. This, however, has not yet been accomplished, and all I can
do is to record the following captures of the moth at light in Para, all males, I
believe, and all in nearly perfect condition : one at Mira Mar, three miles down
the river, in March 1912 ; two on the walls of the S. Braz market in June of
that year ; another subsequently taken by my friend T. T. Dyer in 1917, and
the last falling to me in January 1920.
It will be noted that many of my records date back to 1912, which, though
so wet, rain falling on 323 days, was by far the best year I have yet experienced
in Para or elsewhere for Sphingidae. I find that I recorded 66 species between
April 8 and July 31, and no fewer than 51 in the first 53 days of that period.
658. Xylophanes chiron nechus. (Plate 8.)
R. & J. p. 697.
One of the most showy of the genus in Para in its livery of emerald-green —
a sadly fugitive colour — and at the same time one of the commonest, the moth
Xylophanes cosmius.
R. & J. (1906).
Of this rare species, I became the lucky possessor of the first female known,
a large specimen with a broad forewing considerably hooked at the apex, and
in absolutely perfect condition. This was taken by a Mr. Hammerton in his
house at Manaos in 1912, who most kindly gave it to me, and it is now in the
Tring Museum collection.
Novitates Zoolooicae XXVII. 1920. 413
frequently occurring at electric lamps. The larva is often found on Palicourea
grandijolia, on various species of Psychotria and Spermacoce, all Rubiaceous
plants, and, by way of showing an independence from the general rule adopted
by its genus, has also several times been found on plants belonging to the Order
Icacinaceae. The rather small green egg has often been found on such plants,
and the little glossy green larva resulting from it, with its comparatively slow
growth, has often received the greatest attention, leaving me in suspense as
regards its identity for a considerable time.
In the early instars the marks are faint, the skin thin, glossy, and semi-
transparent, the muscular tissues clearly visible, and only the last two or three
side-stripes indicated very obliquely tailwards in a lighter key. In the third
and fourth instars its identity is unmistakable, a couple of ocelli adorning each
side.
In the last stage these white ocelli in their crimson rings, finely outlined
in black, on segments 5 and 6 which are swollen, constitute a special feature.
A rather more elongate patch of lemon-yellow in some examples, but not
commonly, similarly adorns segment 7, and the customary dorsal area enclosure
is suggested by an interrupted series of three yellow spots on each succeeding
segment. The band leading up to the horn is always the most pronounced in
yellow or white, and is strongly edged above with black. There is also a fine
but much interrupted medio-dorsal black line or series of black marks, the
indication of some 5 side-stripes of a lighter hue than the ground-colour, which
develops from plain green to a very light blue-green tint. The horn, which is
long in early days and light- tipped, becomes stout in the last instar and terminates
with a sharply down-turned black spike. This is grey at the sides and roughened
with pink tubercles above and below. The legs are pink and the spiracles light.
The larva tapers considerably to the head, and while laving itself with a sticky
froth prior to pupation completely changes in colour, turning to an olive-brown
with a prominent black patch or two on each segment.
The pupa is of the normal Xylophanes design and colour but exceptionally
long in the head-piece, and possesses a rather flat and well-developed cremaster,
which is, nevertheless, pointed and insignificant compared with those of the
foregoing species.
Several varieties of dipterous parasites associate themselves with the
species, and from a large and apparently healthy pupa I recently bred a single
fly with the dimensions of a blue-bottle.
Length of proboscis in female moth 2 in.
664. Xylophanes tersa. (Plates T.Z.S.)
R. fe J. p. 703.
Little more need be said of this species beyond recording the fact that it
is normal in Para, as elsewhere, and as common at light as it is known to be in
other parts of the continent.
The larvae frequent several species and allies of Spermacoce (Rubiaceae)
at roadsides and on the banks of ditches, etc., and 1 once induced one to eat a
vine leaf. Though often dark brown, they are here as frequently of a blue-green
tint like the leaves, and are then generally to be found by day on the green
27
414 Novitates Zoolooicae XXVII. 1920.
stalks. The frass is often light green and lined, but very irregular in size and
form.
The pupa is distinguished by its sharp and narrow cremaster, and generally
has much black on the wing-cases. The moth when at rest, in common with
other species of the genus, holds its narrow wings spread out at a wide angle.
Length of proboscis in male moth 1J in.
667. Xylophanes elara.
R. A J. p. 704.
This appears to be a distinctly rare moth in Para, only two perfect specimens
having occurred at light in 1912, one being recorded for the month of August.
Like loelia in size and shape, it is characterized by its delicate sage-green colour
and a small dark orbicular spot in the centre of each forewing.
It can hardly be other than a Rubiaceous feeder, and is probably nourished
on some form of Spermacoce, but here once again the early stages remain to
be discovered.
675. Xylophanes loelia. (Plate 8.)
R. & J. p. 710.
A species resembling a fawn-coloured but less strongly marked edition of
tersa, with salmon-pink instead of yellow on the hindwings, and almost equally
common at light in Para.
The larva, which is green when young, with a couple of yellow lines enclosing
the dorsal area and a straight horn, becomes ochreous-brown with a series of dark
spots to mark the mesial line, and terminates with a prominent dark and distinctly
curved horn in the last stage. Some 5 or 6 dark-brown side-stripes are visible,
and the dark lines which now enclose the brown and spotted dorsal area are
interrupted on segment 5 with a light and dark ocellus, half hidden in the skin-
fold and giving the creature a distinctly wicked and deadly appearance, more
so than in the case of tersa.
It feeds on several varieties of Spermacoce (Rubiaceae), which literally cover
many of our grassy travessas ; and, like other species of this genus that are
secretive and hidden by day, the larva is best obtained by exploring such regions
with a lantern after dark, when it is usually to be found high up on the extremities
of the plant, and is readily detected among the small green leaves.
672. Xylophanes maculator wolfi.
R. & J. p. 707.
A species unknown in Para, and the last of my six extras. On March 7,
1917, during my week's stay at Iquitos, I had the good fortune to take the first
female known of this rare Peruvian subspecies. I found it by day on the wire
gauze covering the verandah of the house of Mr. and Mrs. Harrison, with whom
I was stopping.
The moth was in perfect condition, and thinking that it might possibly
be a new species, I sent it to my friend Mr. Preston Clark, who identified it
as above.
Novitates Zoologicae XXVII. 1920. 415
The pupa, though like tersa, has a lighter dorsal stripe and much less black
on its wing-cases ; the sharp-pointed cremaster, too, is longer and stouter.
Length of proboscis in male moth nearly H in.
677. Xylophanes thyelia.
R. & J. p. 711.
Of this closing species, which was moderately common at light in Para in
1912 but only occasionally seen since, I have once again to confess my ignorance
of its larva, and regret my inability up to date to record anything of its early
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Rubiaceae —
Palicourea grandifolia
Also Psychotria and Spermacoce
Icacinaceae sp. ? several times
Rubiaceae — ■ Spermacoce, several
species
Rubiaceae — Spermacoce as above
Vitaceae — once thrived in captivity
on Cissus
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General and common at light in
Para. Frequently bred from larvae.
Occasionally " stung " by both
diptera and hymenoptera
General and very common at
light in Para. Larvae frequently
found when searched for
Rare in Para. Two specimens
taken at light in eight years.
Larvae undiscovered
Common at light in Para.
Larvae freely obtained by search-
ing after dark with a lantern
Only occasionally at light in
Para. Larvae undiscovered
8
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Xylophanes
Xylophanes
Xylophanes
Xylophanes
Plate 8, fig. 6,
a to/
Plate 8, fig. 3,
a, b
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424
EXPLANATION OF PLATE I.
1. Cocytius cluentius :
a, 3rd instar.
b, 4th „
c, d, 5th ,,
e, broken frass.
2. Cocytius dwponchel :
a, 3rd instar.
b, c, 5th „
3. Protoparce florestan :
at full growth.
4. Protoparce hannibal :
a, b, final instar.
NOVITATES ZOOLOGICAE, VOL. XXVII. 1920.
PL. I.
MENPES PHESS
A. Miles Moss pinx.
EXPLANATION OF PLATE II.
1 . Protoparce rustica rustica :
a, b, final instar.
c, d, frass.
2. Protoparce albiplaga :
at full growth.
3. Protoparce perplexa :
final instar (not black enough, too blue).
4. Pholus jasciatus :
at full growth.
5. Isognathus scyron :
on emergence from egg, magnified 7 times
(not black enough).
6. Cocytius cluentius :
pupa.
7. Protoparce florestan :
pupa,
8. Protoparce hannibal :
pupa.
NOVITATES ZOOLOGICAE, VOL. XXVII. 1920.
PL. II.
MENPES PRESS, LONDON.
A, Miles Mo
EXPLANATION OF PLATE III.
1 . Protambulyx strigilis :
a, b, c, final instar, with cachew leaf.
d, front of head.
e, pupa.
2. Protambulyx strigilis :
when feeding on Rhus (Anacardiaceae).
3. Protoparce albiplaga :
young larva.
4. Isognathus swainsoni subsp. ?
5. Isognathus caricae :
a, 1st instar.
b, 2nd „
c, 4th „
d, 5th
6. Isognathus leachi :
on emergence from egg, magnified 7 times.
N0V1TATES ZOOLOGICAE, VOL. XXVII. 1920.
PL. III.
(
MENPtS PRESS, LONDON.
A. Mil, W
EXPLANATION OP PLATE IV.
1 . Pseudosphinx tetrio :
a, 1st instar, on emergence from egg.
b, 2nd „
2. Isognathus leachi :
a, 1st instar.
b, 3rd „
c, 4th „
d, 5th „
3. Isognathus excelsior :
5th instar.
4. Isognathus menechus :
a, 2nd instar.
b, 3rd „
c, 4th ,, (4c is rather too brightly red).
d, 5th „
5. Isognathus scyron :
a, 1st instar.
b, 2nd „
c, 3rd „
d, 5th „
6. Isognathus mossi :
a, 3rd instar.
b, 4th „
c, 5th „
7. Isognathus swainsoni subsp. ? :
o, pupa.
b, pupa.
NOVITAThS ZOOLOGICAL, VOL. XXVI 1. !!)-'<».
PL. IV
MENPES PRESS, LONDON.
.*). Miles w is -. pin i
%
i* 7
EXPLANATION OF PLATE V.
1. Oryba kadeni :
a, 1st instar.
b, 2nd „
c, 3rd „
d, e, 4th
/, 9, 5th „
N.B.— Fig. 1./ ought to be of a
brighter cadmium yellow.
h, frass.
j, pupa.
2. Oryba achemenides :
a, 2nd instar.
b, 3rd „
C, 4th „
d, e, 5th
3. Xylopfianes guianensis :
frass.
4. Xylophones mossi :
frass.
NOVITATES ZOOI.OGICAE, VOL. XXVII 1920
PL. V
la
'••>•
Id
MENPES PRESS. LONDON
A. Miles Moss pin v.
NOV1TATES ZOOLOGICAE, VOL. XXVII 1H20.
1JL. VI.
MENPES PRESS LONDON
A. M..
EXPLANATION OF PLATE VI.
1. Leucorkampha ornatus :
a, egg on Zscholckea.
b, 1st instar.
c, 2nd „
d, 3rd „
e, f, g, 4th „
h, j, 5th „
2. Madoryx pluto :
a, b, 4th instar : on Miconia.
c, d, 5th „
e, pupa.
Nov
1TATES ZOOI.OGICAE, VOL. XXVI 1. V.)iO.
PL. VII.
MENPES PRESS, LONDON.
A. Miles Moss piti i .
U . ttW» ■ &
EXPLANATION OF PLATE VII.
1 . Grammodia caicus :
a, b, 3rd instar : on Echites.
c, d, 5 th „
2. Erinnyis obscura obscura :
a, b, final instar.
3. Erinnyis crameri :
a, 3rd instar.
b, 5th „
4. Epistor lugubris lugubris :
a, 3rd instar.
b, 5th „
5. Epistor ocypete :
final instar.
6. Epistor gorgon :
a, final instar.
6, pupa.
7. Aleuron iphis or neglectum :
final instar.
8. Enyo japix japix :
a, 4th instar.
b, c, 5th
d, pupa.
9. Sesia titan :
a, b, final instar.
10. Sesia jadus :
final instar.
1 1 . Sesia ceculus :
final instar : on Sabicea.
12. Sesia ceculus :
final instar : on Ourouparia,
13. Perigonia lusca f. restitula :
final instar.
14. Hemeroplanes invvs :
a, 3rd instar.
b, 5th
34
EXPLANATION OF PLATE VIII.
1 . Xylophanes mossi :
a, 3rd instar.
b, 4th ,, with frass.
c, d, 5th ,,
2. Xylophanes anubus :
a, 4th instar.
b, 5th ,, (rather too dark and small).
3. Xylophanes loelia :
a, 4th instar.
6, 5th „
4. Xylophanes guianensis :
a, 4th instar.
b, 5th „
c, pupa.
5. Xylophanes porcus continentalis :
a, 4th instar.
b, 5th „
c, pupa.
6. Xylophanes chiron nechus :
a, 2nd instar.
b, 3rd „
c, 4th „
d, e, 5th „
/, pupa.
NOVITATES ZOOLOGICAE, VOL. XXVII. 1920.
PL. VIII.
MENPtS PRESS. LONDON
I Miles Moss pinx
EXPLANATION OF PLATE IX.
1 . Protoparce perplexa :
a, 2nd instar.
b, 3rd „
c, 4th „
d, 4th instar ; variety as found on Aegiphila cuspidata.
2. Protoparce albiplaga :
a, 3rd instar.
b, 4th „
3. Protoparce hannibal, as found on Aegiphila elata.
4. Neogene dynaeus :
a-d, varieties, full-grown ; Pernambuco.
5. Leucorhampha triptolemus :
a, full-grown.
b, yellow variety.
6. Eupyrrhoglossum sagra :
a, 4th instar.
b, 5th „
7. Pholus anchemolus :
a, 2nd instar.
b, 3rd „
8. Pholus eacus :
a, 4th instar.
b, 4th „
c, full-grown.
NOV1TATES ZOOLOGICAE. VOL. XXVII. I92O.
PI. IX.
A Miles Moss pinx
\K
EXPLANATION OF PLATE X.
1 . Epistor cavifer :
a, 3rd instar.
b, 4th „
c, full-grown.
2. Isognathus mossir
a, 1st instar.
b, 2nd „
c, 3rd „
d, 4th „
e, full-grown.
3. Isognathus allamandae :
a, 1st instar.
b, 3rd „
c, full-grown.
4. Pachylia resumens :
a, 3rd instar.
6, 4th „
c, full-grown.
d, pupa.
5. Epistor lugubris (black-marked variety).
6. Epistor ocypete (pink-marked variety).
7. Leucorhampka ornatus :
4th instar.
8. Erinnyis lassauxi :
a, 3rd instar.
b, 4th „
c, full grown.
9. Protambidyx strigilis :
variety.
10. Protambulyx eurycles :
full-grown.
1 1 . Pholus vitis :
3rd instar.
12. Erinnyis oenotrus :
a, 4th instar.
6, full grown.
NoVITATES ZoOLOGICAK. VOL. XXVII. Iy20
*■■': *
PI. X.
12b
12a
/ITTY & SEABORNF, LTD.
LONDON,
A Milt s .l/'is-, pinx.
PLATE XI.
J[AP of/LtJ>tsfr*ct
^Y~-
I i
£*4jf4t sA. #1 e/< S
Novttates Zoolooicae XXVII. 1920 425
TYPES OF BIRDS IN THE TRING MUSEUM.
By ERNST HARTERT, Ph.D.
B. Types in the General Collection.
Continued from Novitates Zoolooicae, 1919, p. 178.
NECTARINIIDAE.
339. Aethopyga seheriae owstoni Rothsch. = Aethopyga seheriae owstoni.
Acthopyga seheriae owstoni Rothschild, Bull. B.O. Club, xxv. p. 32 (Nauchau Island, Kwangtung,
South China).
Type: c? ad., Nauchau Island, 6. i. 1907. Collected by Alan Owston's
collectors. No. 10.
340. Aethopyga seheriae tonkinensis Hart. = Aethopyga seheriae tonlcinensis.
Aethopyga seheriae tonkinensis Hartert, Bull. B.O. Club, xxxviii. p. 7 (1917 — -Yen-Bai, Tonkin).
Type: <? ad., Yen-Bai, Tonkin, 7.ix.l911. N. Kuroda Coll.
341. Aethopyga siparaja niasensis Hart. = Aethopyga siparaja niasensis.
Aethopyga siparaja niasensis Hartert, Orn. Monatsber. vi. p. 92 (1898 — Nias).
Type : <$ ad., Gunong Sitolie, Nias, vii.1897. Raap leg.
342. Aethopyga latouchii Slater = Aethopyga christinae latouchii.
Aethopyga latouchii Slater, Ibis, 1891, p. 43 (Swatow).
Types : ^$ ad., Chiong P6, Swatow, January 1888. J. D. Latouche leg.
(The genera Urodrepanis and Eudrepanis are founded on differences in the
shape of the middle tail-feathers in the male, while females cannot be separated
generically from those of typical Aethopyga. I therefore do not recognize them.)
343. Cinnyris afra graueri Neum. = Cinnyris afra graueri.
Cinnyris afra graueri Neumann, Bull. B.O. Club, xxi. p. 55 (29. ii. 1908 — ■" Western Kivu Volcanoes ").
Type : <$ ad., " Vorberge der westlichen Kivu-Vulkane, im Urwalde, 2,400
m., 21.viii.1907." Rud. Grauer leg. No. 1,040.
Of this Cinnyris schubotzi Rchw., Orn. Monatsber., March 1908, p. 47, is a
synonym, though graueri may have only a day's priority.
f 344. Cinnyris ansorgei Hart. = Cinnyris reichenowi Sharpe.
Cinnyris ansorgei Hartert, in Ansorge's Under the African Sun, p. 350. pi. ii. fig. 1 (1899 — Nandi).
Type : <$ ad., Nandi, E. Africa, 16.iii. 1898. W. J. Ansorge leg.
Though, at the time, believed to be distinct by Reichenow and Neumann,
the supposed differences from reichenowi cannot be maintained.
426 NoVITATES ZOOLOOICAE XXVII. 1920.
345. Cinnyris chloropygia bineschensis Neum. = Cinnyris cMoropygia bine-
schensis.
Cinnyris chloropygia bineschensis Neumann, Orn. Monatsber. 1903, p. 185 (" Binescho westlich von
Kaffa am Quellgebiet des Gelo, Sobatsystem ").
Type: <J ad., Village Detchabasa, Binesho, 22. iv. 1901. Oscar Neumann
leg. No. 1.153.
The differences stated by the author are quite conspicuous, though only one
specimen was obtained.
346. Cinnyris gutturalis inaestimata Hart. = Cinnyris senegalensis inaestimata .
Cinnyris gutturalis inaestimata Hartert, Ansorge's Under the African Sun, p. 351 (" East Africa."
Sic !).
Type : (J ad., Dar-es-Salaam, November 1895.
This form is quite distinct from C. sen. gutturalis of South Africa, as well as
from C. sen. saturatior Rchw. of South -Western Africa, being considerably
smaller than both.
347. Cinnyris alinae vulcanorum Hartert subsp. no v.
(Ex Neumann MS. in Museo Tring.)
Type : <J ad., " Vorberge der westlichen Kivu-Vulkane, im Urwald, 2,400 m.,
26.viii.1907." Rud. Grauer leg. No. 1,107.
Grauer collected 14 adult males, 3 females, and 3 young on the western
Kivu Volcanoes and Karissimbi, as well as west of Baraka. These differ from
Cinnyris alinae alinae of Mt. Ruwenzori (Ronssoro) in having the crown not
purplish blue, merging into green on the nape, but more or less green all over,
a few specimens only approaching C. alinae alinae.
The breast is also of a darker, more blackish brown, thus more in contrast
with the lower abdomen. The females differ in lacking the lemon-yellow pectoral
tufts, which are only indicated by a few yellowish white elongated feathers,
besides which they are smaller and paler on the abdomen.
I have adopted the name proposed in MS. in the Tring Museum and the type
selected by Professor Neumann, who failed to publish the name and description.
348. Cinnyris oritis Rchw. = Cinnyris oritis.
Cinnyris oritis Reichenow, Journ.f. Orn. 1892, p. 190 (Kamerun).
Cotype : <J, Buea, Kamerun, 21. vi. 1891, 950 m. Preuss leg. (Exchanged
from the Berlin Museum.)
349. Cinnyris infrenata Hart. = Cinnyris jugularis injrenata.
Cinnyris injrenata Hartert, Nov. Zool. x. p. 29 (1903— Tukang Besi Islands).
Type: S ad., Tomia, Tukang Besi group, S.E. of Celebes, 23.xii.1901.
Heinrich Kiihn leg. No. 4,419.
350. Cinnyris frenata meyeri Hart. = Cinnyris jugularis meyeri.
Cinnyris frenata meyeri Hartert, Nov. Zool. iv. p. 156 (1897—" Northern Celebes ").
Type : J ad., Menado tua, N. Celebes, 13. iv. 1893. C. W. Curshaw leg.
NOVITATES ZOOLOQICAE XXVII. 1920. 427
351. Cinnyris frenata dissentiens Hart. = Cinnyris jugularis dissentiens.
Cinnyris frenata dissentiens Hartert, Nov. Zool. iii. p. 152 (1896 — Bonthain Peak, South Celebes) ;
Nov. Zool. iv. pp. 155, 156.
Type : (J ad., Indrulaman, Bonthain Peak, October 1895. Alfred Everett
leg.
352. Cinnyris frenata saleyerensis Hart = Cinnyris jugularis saleyerensis,
Cinnyris frenata saleyerensis Hartert, Nov. Zool. iv. p. 156 (1897 — " Insula Saleyer dicta "),
Type: <J ad., Saleyer (Seleyer), November 1895. Alfred Everett leg.
353. Cinnyris clementiae keiensis Stres. = Cinnyris clementiae keiensis.
Cinnyris clementiae keiensis Stresemann, Nov. Zool. xx. p. 309 (1913 — Key Islands).
Type : <J ad., Add, north of Great Key, 20.vii.1900. Heinrich Kiihn leg.
No. 2,792.
354. Cinnyris zenobia buruensis Hart. = Cinnyris clementiae buruensis.
Cinnyris zenobia buruensis Hartert, Bull. B.O. Club, xxvii. p. 12 (1910 — Buru).
Type : £ ad., Bara (Buru), September 1898. Dumas leg.
About the priority of the name clementiae ef. Sherborn and Woodward, Ann.
and Mag. Nat. Hist. (T) vii. 1901, p. 391, Novitates Zoologicae, xx p. 309.
355. Cinnyris biittikoferi Hart. = Cinnyris biittikoferi.
Cinnyris biittikoferi Hartert, Nov. Zool. iii. p. 581 (1896 — Sumba).
Type : <$ ad., Sumba, February 1896. Will. Doherty leg.
This interesting bird resembles very much Cinnyris aurora from the Philippine
Islands ; a comparative study of all forms of Cinnyris will probably lead to its
being classed as a subspecies of C. aurora.
356. Cinnyris Solaris degener Hart. = Cinnyris Solaris degener.
Cinnyris Solaris degener Hartert, Nov. Zool. xi. p. 214 (1904 — South Flores).
Type : <$ ad., Endeh, S. Flores, 12.ix. 1896. Alfred Everett leg. No. 6,039.
357. Cinnyris Solaris exquisita Hart. = Cinnyris Solaris exquisita.
Cinnyris Solaris exquisita Hartert, Nov. Zool. xi. p. 214 (1904 — Wetter Island).
Type : <J ad., Wetter, 30. ix. 1902. Heinrich Kiihn leg. No. 5,609.
358. Arachnothera longirostris prillwitzi Hart. = Arachnothera longirostra
prillwitzi.
Arachnothera longirostris prillwitzi Hartert, Nov. Zool. viii. p. 51 (1901 — Java).
Type : " ? " ad., Mt. Gedeh, Java, 3,000 ft., 10. vii. 1898. Ernst Prillwitz
leg. No. 14.
428 Novitates Zoolooicae XXVII. 1920.
359. Arachnothera longirostxa rothschildi Oort = Arachnothera longirostra
rothsckildi.
Arachnothera longirostra rothschildi van Oort, Notes Leyden Mus. xxxn. p. 195 (1910 — Natuna
Islands, Bunguran).
Type (marked as rothschildi by van Oort, who had only our 10 Natuna
specimens) : $ ad., Bunguran Island, September 1893. Alfred Everett leg.
360. Arachnothera juliae Sharpe = Arachnothera juliae.
Arachnothera julia e Sharpe, Ibis, 1887. p. 451. pi. xiv. (Kina Balu, Borneo).
Type: S ad., Kina Balu, 3,000 feet, 19. ii. 1887. John Whitehead leg.
No. 984.
361. Anthreptes longmari angolensis Neum. = Anlhreptes longmari angolensis.
Anthreptes longmari angolensis Neumann, Journ. f. Orn. 1906. p. 246 (Angola).
Type: <J ad., Duque de Braganza, northern Angola, 31.vii.1903. W. J.
Ansorge leg. No. 838.
This form seems to be all right, but requires further confirmation, because of
its variability.
362. Cinnyris souimanga apolis Hart., subsp. nov.
Subspeciei Cinnyris souimanga souimanga dictae similis sed differt abdomine pallidiore, sulfurescente.
Years ago Lord Rothschild bought from a dealer in Paris, now deceased, a
number of beautiful skins from Madagascar, all labelled " C. O. Madagascar,"
which, judging from the species and subspecies it contained, must mean Cote
occidentale, i.e. west coast of Madagascar. Out of this collection Professor
Neumann described a new form of Abbotornis, calling it Abbotornis schistocercu-s
(Bull. B.O. Club, xxiii. p. 11, 1908), and it contains the light form of Mirajra
hova known to inhabit West Madagascar. In this lot are also three males of
Cinnyris souimanga, which differ from a series of 13 from various other parts
of Madagascar in the Tring Museum, and about as many in the British Museum,
by having the abdomen pale sulphur-yellow instead of more or less rich yellow,
the flanks much paler, not olivaceous, and the ornamental pectoral tufts of a
lighter yellow. Unfortunately the exact locality of these birds is not known,
therefore the name apolis, meaning homeless. It is true that in the description
of Brisson, from whom Gmelin took his souimanga, the abdomen is described as
pale yellow, and that in Audebert & Vieillot's Oiseaux dories it is not bright, not
clear, light, sulphur-yellow as in apolis, but dirty as in aldabranus ; but at that
time specimens were not preserved as they are nowadays, and often faded (perhaps
from spirits), so that the descriptions must be taken cum grano satis.
Type : (J ad., west coast of Madagascar. Purchased in Paris. " Native
name Sony."
363. Anthreptes malaccensis wiglesworthi Hart. = Anthreptes malaccensis
wiglesivorthi.
Anthreptes malaccensis wiglesworthi Hartert, Nov. Zool. ix. p. 209 (1902 — Sulu Islands).
Type : (J ad., Sulu Island, 1. v. 1883. Dr. Powell leg.
NOVITATES ZOOLOGICAE XXVII. 1920. 429
364. Anthreptes hypogrammica intensior Hart. = Antkreptes hypogrammica
intensior.
Anthreptes hypogrammica intensior Hartert, Bull. B.O. Club, xxxviii. p. 27 (1917 — Borneo).
Type : (J ad., Balingean, Sarawak, Borneo, 9. vi. 1903. Brook leg. No. 22.
DICAEIDAE.
365. Dicaeum mysoriense Salvad. = Dicaeum geelvinkianum mysoriense.
Dicaeum mysoriense Salvadori, Ann. Mus. Giv. Genova, vii. p. 945 (1875 — Korido, Misovi = Schouten
Islands).
Cotype : $ ad., " Korido," Schouten Islands, 20. v. 1875. Odoardo Beecari
leg. Specimen " e " of Salvadori's list, marked in the author's handwriting
" Typus " and " nov. sp."
366. Dicaeum geelvinkianum diversum R. & H. = Dicaeum geelvinkianum
diversum.
Dicaeum geelvinkianum diversum Rothschild & Hartert, Nov. Zool. x. p. 215 (1903 — " North coast
of Dutch New Guinea ").
Type : (J ad., Lower Ambernoh (= Mamberano or Rochussen) River.
J. Dumas leg. No. 117.
367. Dicaeum geelvinkianum rosseli R. & H. = Dicaeum geelvinkianum rosseli.
Dicaeum geelvinkianum rosseli Rothschild & Hartert, Bull. B.O. Club, xxxv. p. 32 (December 1914 —
Rossel Island).
Type : (J ad., Rossel Island, Louisiade group, 3.ii. 1898. A. S. Meek leg.
No. 1,362.
368. Dicaeum kiihni Hart. = Dicaeum kiihni.
Dicaeum kiihni Hartert, Nov. Zool. x. p. 25 (1903 — Tukang Besi Islands).
Type : £ ad., Kalidupa, 31. xh. 1901, Heinrich Kiihn leg. No. 4,587.
This may be a subspecies of D. celebicum, and so might D. sanghirense and
sulaense, but a lengthy study of all these forms is necessary to fully understand
their relationship.
369. Dicaeum neglectum Hart. = Dicaeum mackloti neglectum.
Dicaeum neglectum Hartert, Nov. Zool. iv. p. 264 (1897 — Lombok).
Type: $ ad., North Lombok, 2,000 feet, vii. 1896. Alfred Everett leg.
370. Dicaeum mackloti romae Hart. = Dicaeum mackloti romae.
Dicaeum mackloti romae Hartert, Nov. Zool. xiii. p. 300 (1906 — Roma Island).
Type : <$ ad., Roma, lO.viii. 1902. Heinr. Kiihn leg. No. 5,399.
371. Dicaeum apo Hart. = Dicaeum luzoniense apo.
Dicaeum apo Hartert, Bull. B.O. Club, xiv. p. 79 (1904 — Mt. Apo, Mindanao).
Type : <$ ad., Mount Apo, Mindanao, 3,000 feet, x. 1903. John Waterstradt
leg.
28
430 Novitates Zoolooicae XXVII. 1920.
372. Dicaeum bonga Hart. = Dicaeum luzoniense bonga.
Dicaeum bonga Hartert, Bull. B.O. Club, xiv. p. 80 (1904 — Bonga, Samar).
Type : $ ad., Bonga, Samar, Philippine Islands, 18. vi. 1896. John White-
head leg. No. B 631.
373. Dicaeum trigonostigma megastoma Hart. = Dicaeum trigonostigma
megastoma.
Dicaeum trigonostigma megastoma Hartert, Bull. B.O. Club, xxxviii. p. 74 (1918 — Bunguran, Natuna
Islands).
Type : cj ad., Bunguran, 7.x. 1893. Alfred Everett leg.
374. Dicaeum trigonostigma flaviclunis Hart. = Dicaeum trigonostigma
flaviclunis.
Dicaeum trigonostigma flaviclunis Hartert, Bull. B.O. Club, xxxviii. p. 75 (1918 — Java).
Type : ^ ad., Karangbolong, S. Java, April — May 1901. Ernst Prillwitz
leg.
375. Dicaeum sollicitans Hart. = Dicaeum minullum sollicitans.
Dicaeum sollicitans Hartert, Nov. Zool. viii. p. 52 (1901 — Java).
Type : ad., Mt. Gedeh, Java, 3—5,000 feet. Collected between October 1897
and January 1898, by Ernst Prillwitz. No. 73.
Stresemann collected this rare little bird on Bah.
376. Dicaeum nigrilore Hart. = Dicaeum nigrilore.
Dicaeum nigrilore Hartert, Bull. B.O. Club. xv. p. 8 (1904 — Mindanao).
Type : <J ad., Mount Apo, Mindanao, October 1903, 3,000 feet. John
Waterstradt leg. No. W 302 a.
Waterstradt sent us 13 specimens of this very distinct species, all from
Mt. Apo, some of them young. The latter have the crown and forehead of the
same brown colour as the back.
377. Prionochilus inexpectatus Hart. = Prionochilus bicolor inexpectatus*
Prionochilus inexpectatus Hartert, Nov. Zool. ii. p. 64 (1895 — Luzon, Mindoro).
Type : £ ad., North Mindoro, 30.xii. 1894. Alfred Everett leg.
378. Prionochilus Plateni Bias. = Prionochilus xanthopygius plateni.
Prionochilus Plateni Willi. Blasius, Braunschw. Auzeig. No. 37, 12. ii. 1888. p. 335; Ornis, 1888,
p. 313 (Palawan).
Type: <J ad., Puerto Princesa, Palawan, 22.vii.1887. Dr. Platen leg.
(Exchanged from Ad. Nehrkorn.)
* Oberholsor rejects the name Prionochilus because of the earlier name Prionocheilua, and
adopted the name Anaimos Reichenbach, 1883. Though the two names are evidently only different
Latin renderings of the some Greek name, I suppose they are easily distinguishable and should both
be accepted. No nomenclatorial rule demands the contrary.
NOVITATES ZOOLOGICAE XXVII. 1920. 431
• The names of new forms described by Blasius in the Braunschiveigische
Anzeigen, 1888, have priority over the names given by Sharpe in the Ibis, 1888.
Blasius exhibited the Palawan collection, which was the property of Mr. Nehrkorn,
at a meeting of the Braunschweig Natural History Society, and reports of the
meeting were published, with full descriptions of the new birds, in the Anzeigen
of February 12th and March 1st. These descriptions have been republished in
the Omis, 1888, where a full report of the collections is given. Though the
descriptions in the Omis appeared later, those in the Braunschiveigische Auzeigen
were earlier than Sharpe's, which appeared in the April Ibis. Objectionable as
it is for any scientific person to allow diagnoses of new forms to be published for
the first time in a newspaper, whether daily or weekly, or any other periodical
not devoted to science entirely or primarily, such names must be accepted, as
a line cannot be drawn between the various kinds of publications. This is
universally admitted, and such names have been adopted. An exception
therefore cannot be made in the case of Blasius's names, though Sharpe (cf.
for example Hand-list B. v. p. 30) preferred his own.
f 378 a. Prionochilus johannae Sharpe = Prionochilus xanthopygius plateni.
Prionochilus johannae Sharpe, Ibis, April 1888. p. 201. pi. iv. fig. 1 (Palawan).
Type: (J ad., Taguso, Palawan, 25. vi. 1887. John Whitehead leg. No.
1,427.
379. Pristorhamphus versteri meeki R. & H. = Pristorhamphus versteri meeki.
Pristorhamphus versteri meeki Rothschild & Hartert, Bull. B.O. Club, xxix. p. 36 (1911 — Mt. Goliath).
Type : <J ad., Mount Goliath, Eastern Central Dutch New Guinea, 8 . ii . 1911.
A. S. Meek Coll. No. 5,332.
C. Boden Kloss collected specimens on the Utakwa River, from 2,900 to
8,000 feet, in the Snow Mountains, of which Mt. Goliath is part of the eastern
range.
380. Pristorhamphus versteri albescens R. & H. = Pristorhamphus versteri
albescens.
Pristorhamphus versteri albescens Rothschild & Hartert, Bull. B.O. Club, xxix. p. 36 (1911 — Mountains
of British New Guinea).
TvPe : $ ad., Kotoi district, Owen Stanley Mountains, 4,000 feet, 12. viii.
1898. A. S. Anthony leg.
381. Eafa maculata R. & H. = Rhamphocharis maculata.
Eafa maculata Rothschild & Hartert, Nov. Zool. x. p. 448 (1903 — Owen Stanley Range, British New
Guinea).
Type : (? ad.), Eafa district, Owen Stanley Mts., between 1.000 and 3,000
feet, 1902. A. S. Anthony leg. (Purchased from Mcllwraith & McEacham
in London.)
(About the generic name, etc., see Novitates Zoologicae, 1907, p. 478.)
432 Novitates Zoologicae XXVII. 1920.
INCERTAE SEDIS*
382. Parmoptila ansorgei Hart. = Parmoptila voodhonsei ansorgei.
Parmoptila ansorgei Hartert, Bull. B.O. Club, xiv.(p. 72 (1904 — Angola).
Type: £ ad., Golungo Alto, N. Angola, 9. i. 1904. W. J. Ansorge leg.
No. 13.
This subspecies is very closely allied to P. woodkousei woodhousei from Gabun
and Kamerim, differing only in being a little paler, both on the throat and head
and on the upperside, and the wing is about 2 or 3 mm. longer. There is a good
figure of P. w. woodhousei in the Ibis, 1909, plate II.
ZOSTEROFIDAE.
383. Zosterops poliogastra erlangeri Neum. = Zosterops poliogastra erlangeri.
Zosterops poliogastra erlangeri Neumann, Bull. B.O. Club, xxi. p. 60 (1908 — " High mountains of
South Ethiopia, Shoa, Harar, Arussi Mountains, and the Omo region ").
Type : $ ad., Gadut in Gofa, 31. i. 1901. Oscar Neumann leg. No. 733.
384. Zosterops omoensis Neum. = Zosterops omoensis.
Zosterops omoensis Neumann, Orn. Monatsber. 1904. p. 162 (" Taler des Omo-Gebietes ").
Type: <J ad., Senti valley, between Uba and Gofa, 28. i. 1901. Oscar
Neumann leg. No. 690.
I am inclined to think that omoensis must be a subspecies of Z. abyssinicus.
385. Zosterops abyssinica socotrana Neum. = Zosterops abyssinica socotrana.
Zosterops abyssinica socotrana Neumann, Bull. B.O. Club, xxi. p. 59 (1908 — Sokotra).
Type : (J ad., Dahamis, Sokotra, 350 feet, 20.xii.1898. Ogilvie-Grant and
Forbes Coll. No. 190.
This form is distinguished from Z. abyssinica abyssinica by the lighter, more
whitish underside. The difference in the colour of bill and feet is striking in
comparing our skins from Abyssinia and Sokotra, but the feet look dark again
in those from the Wagar mountains, Somaliland.
? t 386. Zosterops smitlii Neum. = Zosterops senegalensis jubaensis.
Zosterops jubaensis Erlanger, Orn. Monatsber. 1901. p. 182 (Damasso, Gurra, Juba River).
Zosterops smithi Neumann, Orn. Monatsber. 1902. p. 139 (Sillul, Bodele, Western Somaliland).
Type : cJ, Bodele, Sillul, l.viii.1894. Donaldson Smith leg. No. 140.
Probably = jubaensis, but topotypical specimens of latter required to be
certain of this.
* The genera Pholidomis Hartl. 1857, Parmoptila Cass. 1859, and Lobornis Sharpe 1874 (the
last evidently not distinct from Parmoptila, having been described from the young) are of very
doubtful systematic position. In the Cat, B. Brit. Mas. x. Sharpe placed them among the Dicaeidae,
before and after " Prionochilus," but in the Hand-list, iv. p. 233, he put them in the Sylviidae,
evidently following Shelley, while Reichenow had them at the end of the Paridae. Neither of these
positions seems to me satisfactory. The bill certainly has a striking resemblance with that of certain
Dicaeidae {Dicaeum), but the strong feet and tarsi and the somewhat hard and scanty, almost scale-
like plumage are utterly different. The strong feet, largo-scaled (not scutellate !) tarsus, and hard
plumage (chiefly in Pholidomis) remove them at onco from the Sylviidae. The feet have certainly
much resemblance to those of the Paridae, but the hard plumage and free nostrils, not overhung
by antrorse feathers, are not at all characters of the Paridae. Perhaps this little group should form
a separate family. It would be very valuable to study the biology and to discover nest and eggs
of these interesting little birds.
NOVITATES ZOOLOGICAE XXVII. 1920. 433
337. Zosterops superciliosa Rchw. = Zosterops senegalensis swpetciliosa.
Zosterops superciliosa Reichenow, Journ. f. Orn. 1892. p. 192 (Kiri and Fadjulli).
Type or Cotype : (J ad., Fadjulli. Emin Pasha leg. (Purchased from
Hartlaub. )
Neumann, Orn. Monatsber. 1904, p. Ill, says that only two specimens, one
in the British, one in the Tring Museum, existed, and he marked ours from Fadjulli
as the type. Probably Reichenow borrowed this from Hartlaub before it came
to Tring. and it was the only one he had seen at the time. Should he have
examined the British Museum specimen as well, ours would be the cotype.
Reichenow did not, and does not nowadays, quote the exact date and number,
etc. , of type specimens.
388. Zosterops kaffensis Neum. = Zosterops virens kaffensis.
Zosterops kaffensis Neumann, Orn. Monatsber. 1902. p. 10 (Kaffa) ; Zosterops virens kaffensis id.,
Journ. f. Orn. 1906. p. 243.
Type: ^ ad., Anderatscha, Kaffa, 1 1 . iii . 1901. Oscar Neumann leg.
No. 994.
389. Zosterops schoana Neum. = Zosterops virens schoana.
Zosterops schoana Neumann, Orn. Monatsber. 1903. p. 185 (Schoa).
Zosterops virens schoana id., Journ. f. Orn. 1906. p. 242.
Type: $ ad., Abuje, province of Gindcherat, Schoa, 3.x. 1900. Oscar
Neumann leg. No. 134.
390. Zosterops westernensis vegeta Hart. = Zosterops lateralis vegeta.
Zosterops westernensis vegeta Hartert, Nov. Zool. vi. p. 425 (1899 — Cape York, N. Queensland).
Type: $ ad., Cape York, 15.vii.1898. Eichhorn leg. (No. 1,941 of the
Meek collections.)
(Mathews, in his latest List of the Birds of Australia, makes vegeta a synonym
of Zosterops lateralis ramsayi. [Zosterops ramsayi Masters, Proc. Linn. Soc.
N. 8. Wales, i. p. 56, 1875, from " Palm Island " in Torres Strait.] When I named
vegeta I was not acquainted with Masters's description, but it does not suit my
vegeta. The middle of the abdomen is whitish and not " light grey," and the
wing measures 56-57, and not over 60 mm. [" 2-4 inches "]. The suggestion that
vegeta is ramsayi therefore cannot be accepted and must remain doubtful until
specimens from " Palm Island " have been examined. Where " Palm Island "
is I do not know, nor does Mathews [in lilt.), as neither our maps nor the Pacific
Ocean Directory give it.
391. Zosterops sumbavensis Guill. = Zosterops intermedia sumbavensis.
Zosterops sumbavensis Guillemard, Proc. Zool. Soc. London, 1885. p. 508 (Sumbawa).
Cotype: " $ ?," Bima, Sumbawa, 14.viii. 1883, specimen b. R. ff. Powell
leg. (Guillemard Collection, made during the voyage of the yacht Marchesa.)
It is evident that the two specimens, a and b, are both discoloured, the
brownish golden coloration not being the natural one. We have similarly
434
Novitates Zoolooicae XXVII. 1920.
discoloured specimens of Z. chloris. Our specimens collected at Tambora
(Doherty) and Bima (Everett) are very closely allied to Z. intermedia intermedia
from South Celebes, but their wings are 2 to 3 mm. longer, the bills larger. This
is therefore a very close subspecies of intermedia ; but it is quite possible that
a complete monographic study of the genus will lead to the grouping of even
intermedia as a subspecies of another previously named species.
392. Zosterops intermedia periplecta Hart., subsp. nov.
Eight specimens of this Zosterops— three from Everett, five from Doherty—
are underneath paler and on the upperside a little more olivaceous green, less
golden than Z. i. intermedia and Z. i. sumbavensis, while the bills are at least as
strong as in the latter, and the wings fully as long and sometimes even 1 or 2 mm.
longer.
Type : <J ad., Lombok, 1,500 feet, May 1896. Alfred Everett leg.
393. Zosterops unica Hart. = Zosterops unica.
Zosterops unica Hartert, Nov. Zool. iv. p. 520 (1897— Nanga Ramau).
Type : adult (sex ?), Nanga Ramau, S. Flores, October 1896. Alfred
Everett leg.
I have so far never seen a second specimen. It might be looked upon as a
subspecies of Z. intermedia, but in a genus like Zosterops characters like the
bright-yellow rump patch, black tail, smaller size, and apparently deep black
bill suggest a separate species.
394. Zosterops flavissima Hart. = Zosterops flavissima.
Zosterops flavissima Hartert, Nov. Zool. x. p. 29 (1903— Tukang Besi Islands).
Type : (J ad., Binungku, Tukang Besi Islands, 9.xii.l901. Heinrich Kiihn
leg. No. 4,215.
395. Zosterops obstinatus Hart. = Zosterops obstinatus obstinatus.
Zosterops obstinatus Hartert, Nov. Zool. vii. p. 238 (1900— Batjan).
Type : ? ad., Batjan, 4,000 feet, September 1897. Will. Doherty leg.
396. Zosterops obstinatus ternatanus Stres. = Zosterops obstinatus ternatanus.
Zosterops obstinatus ternatanus Stresemann, Nov. Zool. xxi. p. 139 (1914 — Ternate).
Type : $ ad., Ternate, 3—4,000 feet, September 1896. William Doherty leg.
397. Zosterops obstinatus seranensis Stres. = Zosterops obstinatus seranensis.
Zosterops obstinatus seranensis Stresemann, Nov. Zool. xxi. p. 139 (1914 — Seran).
Type : J ad., Gunong Pinaia, Ceram (Seran), 6,000 feet, 15.viii. 1911. Erwin
Stresemann leg. No. 878.
(In Stresemann's article on the birds of Ceram, Novitates Zoologicae,
1914, no mention is made of Zosterops tudjuensis Oort, Notes Leyden Mus. xxxiv.
Novitates Zoological XXVII. 1920. 435
p. 65, 1912, from the Pulu Tudju group north of Ceram. Though the description
does not agree with Z. o. seranensis, it must be a near ally, and as the Pulu Tudju
group appears to be very close to Ceram, should be included in the Ceram Fauna.
Perhaps obstinatus and its allies, tematanus and seranensis, might be looked upon
as subspecies of Z. chloris /)
398. Zosterops adiniralitatis R. & H. = Zosterops fuscicapilla admiralitatis.
Zoslerops admiralitatis Rothschild & Hartert, Bull. B.O. Club, xxxiii. p. 108 (1914 — Manus, Admiralty
Islands) ; cf. also Nov. Zool. 1914. p. 298 !
Type : ^ ad., Manus, 23. ix. 1913. Eichhorn leg. (No. 6,132 of the A. S.
Meek collections.)
399. Zosterops semperi owstoni Hart. = Zosterops semperi owstoni.
Zosterops semperi owstoni Hartert, Nov. Zool. vii. p. 2 (1900 — Ruk Island).
Type : ad., Truk (or Ruk) Island, Carolines, 7. v. 1896. (Collected by Alan
Owston's Japanese collectors.)
400. Zosterops meeki Hartert = Zosterops meeki.
Zosterops meeki Hartert, Nov. Zool. v. p. 528 (1898 — Sudest Island, Louisiade group).
Type : <J ad., Sudest Island, 18. iv. 1898. A. S. Meek leg. No. 1,753.
We have now 10 specimens of this beautiful species.
401. Zosterops palpebrosa alani Hart. = Zosterops palpebrosa alani.
Zosterops palpebrosa alani Hartert, Bull. B.O. Club, xv. p. 45 (1905 — South Dionisio, Volcano Islands,
south of the Bonin group).
Type: <J ad., South Dionisio, 29. v. 1904. Collected by Alan Owston's
Japanese collectors.
402. Zosterops palpebrosa foghaensis Stres. = Zosterops palpebrosa foghaensis.
Zosterops palpebrosa foghaensis Stresemann, Nov. Zool. xix. p. 347 (1912 — Gunong Fogha, Buru).
Type and unique specimen : $ ad., Gunong Fogha, 5,500 feet, 28. ii. 1912.
Erwin Stresemann leg. No. 1,091.
403. Zosterops palpebrosa harterti Stres. = Zosterops palpebrosa harterti.
Zosterops palpebrosa harterti Stresemann, Nov. Zool. xix. p. 347 (1912 — Alor).
Type : cj ad., Alor, 30 . iii . 1897. Alfred Everett leg.
f 404. Zosterops clara Sharpe = Zosterops atricapilla Salvad.
Zosterops clara Sharpe, Ibis, 1888. p. 479 (Kina Balu, Borneo).
Type : <J ad., Mt. Kina Balu, 4,000 feet, 9. iii. 1888. John Whitehead leg.
No. 2,179.
(Sharpe, when describing Z. clara, did not compare it with Z. atricapilla
(Salvadori, Ann. Mus. Genova, xiv. p. 215, 1879), which he quite overlooked-
After comparing two skins from Mt. Korinchi, Sumatra, collected by Robinson
and Kloss, with six from Kina Balu, I must agree with Finsch, who united clara
436 NOVITATES ZOOLOGICAE XXVII. 1920.
and atrknpiUa. It is of course possible that slight differences may become
obvious between the Sumatran and Bornean birds, but so far we are not justified
in separating them.)
405. Zosterops vellalavella Hart. = Zosterops vellalavella.
Zosterops vellalavella Hartert, Bull. B.O. Club, xxi. p. 106 (1908— Vella Lavella Island, Solomon
group).
Type : S ad., Vella LaveUa, 26. ii. 1908. A. S. Meek Coll. No. 3,856.
406. Zosterops kiihni Hart. = Zosterops kiihni.
Zosterops kiihni Hartert, Bull. B.O. Club, xvi. p. 82 (1906— Amboina).
Type: cj ad., Amboina, 16. ii. 1906. Heinrich Kiihn leg. No. 7,280.
407. Zosterops kulambangrae R. & H. = Zosterops rendovae kulambangrae.
Zosterops kulambangrae Rothschild & Hartert, Nov. Zool. viii. p. 180 (1901— Kulambangra, Central
Solomon Islands).
Type : $ ad., Kulambangra, 13. hi. 1901. A. S. Meek Coll. No. 2,875.
408. Zosterops luteirostris Hart. = Zosterops luteirostris.
Zosterops luteirostris Hartert, Bull. B.O. Club, xiv. p. 61 (1904 — Gizo, Solomon Islands).
Type : (J ad., Gizo, 2.xi. 1903. A. S. Meek Coll. A. 724.
409. Zosterops aignani Hart. = Zosterops aignani.
Zosterops aignani Hartert, Nov. Zool. vi. p. 210 (1899— St. Aignan Island, Louisiado group).
Type : <J ad., St. Aignan, 7.xii.l897. A. S. Meek Coll. No. 1,132.
410. Zosterops floridana R. & H. = Zosterops floridana.
Zosterops floridana Rothschild & Hartert, Nov. Zool. viii. p. 180 (1901— Florida Island, Solomon
Islands).
Type : <J ad., Florida Island, 28.xii. 1900. A. S. Meek Coll. No. 2,704.
411. Zosterops whiteheadi Hart. = Zosterops whiteheadi whiteheadi.
Zosterops whiteheadi Hartert, Bull. B.O. Club, xiv. p. 13 (1903— Lepanto district, N. Luzon).
Type : <J ad., Lepanto, N. Luzon, 5,000 feet, 14. xii. 1894. John Whitehead
leg. No. 819.
412. Zosterops whiteheadi vulcani Hart. = Zosterops whiteheadi vulcani.
Zosterops whiteheadi vulcani Hartert, Bull. B.O. Club, xiv. p. 14 (1903— Mt. Apo, South Mindanao).
Type : <J ad., Mt. Apo, 8,000 feet, iv. 1903. Walter Goodfellow leg.
413. Zosterops japonica insularis Ogawa = Zosterops insular is.
Zosterops japonica insularis Ogawa, Annol. Zool. Japon. v. p. 186 (1905— Islands of Tanega [Tane-
gashima] and Yaku, south of Japan).
Type : <J ad., Tanega, 12. xi. 1904. Collected by Alan Owston's Japanese
collectors. (No. 1,330.)
Novttates Zooloqicae XXVII. 1920. 437
I cannot consider this very distinct form to be a subspecies of japonica. In
the coloration of the sides it is somewhat intermediate between the latter and
erythropleura.
414. Zosterops alberti R. & H. = Zosterops alberti.
Zosterops alberti Rothschild & Hartert, Nov. Zool. xv. p. 364 (1908 — San Christoval, Solomon Islands).
Type : <$ ad.; San Christoval, 25. iv. 1908. A. S. Meek Coll. No. 4,078.
415. Oreozosterops javanica elongata Stres. = Oreozosterops javanica elongata.
Oreozosterops javanica elongata Stresemann, AW. Zool. xx. p. 366 (1913 — Bali).
Type: $ ad., Gunong Bratan, Bali, 27. i. 1911. Erwin Stresemann leg.
No. 211.
(It is perhaps as well to recognize the genus Oreozosterops.)
416. Zosterops goodfellowi Hart. = Oreozosterops goodfellowi.
Zosterops goodfellowi Hartert, Bull. B.O. Club, xiv. p. 13 (1903 — Apo Volcano, Mindanao).
Type : £ ad., Mt. Apo, 8,000 feet, iv.1903. Walter Goodfellow leg. No.
124 a.
417. Zosterops superciliaris Hart. = Oreozosterops superciliaris.
Zosterops superciliaris Hartert, Nov. Zool. iv. p. 172 (1897 — South Flores).
Type : $ ad., South Flores, above 3,000 feet, October 1896. Alfred Everett
leg.
418. Oreozosterops pinaiae Stres. = Oreozosterops pinaiae.
Oreozosterops pinaiae Stresemann, Bull. B.O. Club, xxxi. p. 5 (1912 — " Central Mountains of Middle
Ceram, above 4,000 feet ").
Type: <$ ad., Gunong Pinaia, Central Ceram, 7,500 feet, 17. viii. 1911.
Erwin Stresemann leg. No. 877.
419. Zosterops crassirostris Hart. = Pseudozosterops crassirostris.
Zosterops crassirostris Hartert, Nov. Zool. iv. p. 172 (1897 — South Flores).
Type : <$ ad., South Flores, 3,500 feet, 28.x. 1896. Alfred Everett leg.
(I am adopting the genera Oreozosterops. Pseudozosterops, and Lophozosterops
at least provisionally, as in the Hand-list of B. v. p. 20, and by Stresemann,
NOVITATES ZOOLOGICAE, XXi. p. 138.)
420. Chlorocharis squamiceps Hart. = Pseudozosterops squamiceps.
Chlorocliaris squamiceps Hartert, Nov. Zool. iii. p. 70 (1896 — Bonthain Peak, South Flores).
Type : <J ad., Bonthain Peak, 6,000 feet, October 1895. Alfred Everett leg.
421. Chlorocharis emiliae Sharpe = Chlorocharis emiliae.
Chlorocharis emiliae Sharpe, Ibis, 1888. p. 392 (Mt. Kina Balu, N. Borneo).
Type: 2 ad., Kina Balu, 8,000 feet, 27. ii. 1888. John Whitehead leg.
No. 2,077.
■"8 NOVITATES ZOOLOGICAE XXVII. 1920.
422. Lophozosterops dohertyi Hart. = Lophozosterops dohertyi dohertyi.
Lophozosterops dohertyi Hartert, Nov. Zool. iii. p. 168 (1896— Sumbawa).
Type : <J ad., Tambora, Sumbawa, 1,000 feet, April— May 1896. William
Doherty leg.
423. Lophozosterops subcristatus Hart. = Lophozosterops dohertyi subcristatus.
Lophozosterops subcristatus Hartert, Nov. Zool. iv. p. 171 (1894— Hills of South Flores).
Type : <J ad., South Flores, above 3,000 feet, x. 1896. Alfred Everett leg.
424. Tephras ruki Hart. = Tephras ruki.
Tephras ruki Hartert, Bull. B.O. Club, vii. p. v. (1897— Ruk Island, Carolines).
Type : $ ad., Ruk (Truk), 25. xi. 1895. Alan Owston's Japanese collectors.
No. B 15.
425. Hypocryptadius cinnamomeus Hart. = Hypocryptadius cinnamomeus.
Hypocryptadius cinnamomeus Hartert, Bull. B.O. Club, xiv. p. 13 (1903— Mt. Apo, Mindanao).
Type: $ ad., Mt. Apo, 8,000 feet, April 1903. Walter Goodfellow leg.
No. 121.
CERTHIIDAE
f 426. Certhia familiaris pyrenaica Ingram = Certhia familiaris costae.
Certhia familiaris pyrenaica Ingram, Ibis, 1913. p. 549 (near Cauterets, Central Pyrenees).
Types : $<$, Reine Hortense, 1,400 m., close to Cauterets, 30.xii. 1906,
Pine woods of the Colde Riou, 1,600 m., above Cauterets, 6.ii. 1907. (The
supposed § is the most typical male and is from the " Sapiniere de Riou.")
(In his very interesting article in Ibis, 1913, Ingram has correctly shown
that costae, the Alpine form, is separable from macrodactyla. In my book I had
united it with the latter for want of material. I cannot, however, agree that
" pyrenaica " is again separable — it seems to me to be quite like the Alpine form.)
427. Certhia familiaris japonica Hart. = Certhia familiaris japonica.
Certhia familiaris japonica Hartert, Nov. Zool. 1897. p. 138 (Hondo, Japan).
Type : " <J " (?), Iwaki, Hondo, Japan. From Alan Owston.
428. Certhia familiaris corsa Hart. = Certhia familiaris corsa.
Certhia familiaris corsa Hartert, Vog. pal. Fauna, p. 320 (1905 — Corsica).
Type : (J ad., Vivaria, Corsica, 6. i. 1884. John Whitehead leg. No. 6,184.
(Reichenow is of opinion that this form is a subspecies of C. brachydactyla,
but it is a familiaris. It inhabits only the elevated mountain forests, during the
breeding season. Wharton and Backhouse, however, saw Creepers in the chestnut
groves ; and if they should breed there, it is quite conceivable that those birds
might be a form of brachydactyla, and that, as elsewhere, two species occurred
in Corsica.)
NOVTTATES ZoOLOGICAE XXVII. 1920. 439
429. Certhia familiaris tianschanica Hart. = Certhia jamiliaris tianschanica.
Certhia familiaris tiansclianica Hartert, Vog. pal. Fauna, i. p. 321 (1905 — " Tianschan ").
Type: <J, Aksu, 19. ii. 1902. Kutzenko leg. No. 1,801.
430. Certhia brachydactyla ultramontana Hart. = Certhia brachydactyla ultra-
montana.
Certhia brachydactyla ultramontana Hartert, Vog. pal. Fcmna, i. p. 324 (1905 — " Siideuropa siidlich
der grossen Gebirgsketten : Italien, Spanien, Siiddalmatien, Grieehenland ").
Type: $ ad., Panzano, near Chianti, 3.x. 1902. Ex Squilloni. No. 656.
Inhabits also southern France (Ingram, Ibis, 1913).
431. Certhia brachydactyla mauritanica With. = Certhia brachydactyla
mauritanica.
Certhia brachydactyla mauritanica Witherby, Bull. B.O. Club, xv. p. 35 (1905 — Tunisia, Algeria).
Type : <J ad., Ai'n-Draham, North Tunisia, 13. iv. 1903. Paul Spatz leg.
432. Certhia familiaris harterti Hellm. = Certhia brachydactyla harterti.
Certhia familiaris harterti Hellmayr, Journ.f. Orn. 1901, p. 189 (" Kleinasien ").
Type: ad., Alum-Dagh, Asia Minor, 28.xii.1868. T. Robson leg. (Ex
Coll. J. Elwes.)
433. Salpornis Emini Hartl. = Salpornis spilonota emini.
Salpornis Emini Hartlaub, Proc. Zool. Soc. London, 1884. p. 415. pi. 37 (1884 — Langomeri, Equatorial
Province) ; Salpornis Salvadorii orientalis, id., Journ.f. Orn. 1889. p. 116 (New name for S. emini).
Type of both names : $ ad., Langomeri. Emin Pasha leg.
434. Salpornis spilonota erlangeri Neum. = Salpornis spilonota erlangeri.
Salpornis spilonota erlangeri Neumann, Orn. Monatsber. 1907. p.52 (Kaffa and Djamdjam, S. Ethiopia).
Type : $ ad., Anderatsha, Kaffa. 16. hi. 1901. Oscar Neumann leg.
435. Climacteris placens meridionalis Hart. = Climacteris placens meridionalis.
Climacteris placens meridionalis Hartert, Bull. B.O. Club, xxi. p. 27 (1907 — Mountains of British
New Guinea).
Type : $ ad., Owgarra, Angabunga River, 6—8,000 feet, 29. i. 1905. A. S.
Meek leg. No. A 2,038.
SITTIDAE.
436. Sitta europaea britannica Hart. = Sitta europaea britannica.
Sitta europaea britannica Hartert, Nov. Zool. vii. p. 526 (1900 — England, type Tring).
Type : <J ad., Tring Park, 13.x. 1898. Ernst Hartert leg.
440 NOVITATES ZOOLOGICAE XXVII. 1920.
437. Sitta rupicola Blanf. = Sitta neumayer rupicola.
Sitta rupicola Blanford, Ibis, 1873. p. 87 (" In montibus Persicis praesertim in Elburg aaxa scopu-
losque frequentans ").
Type : $ juv., Lura Valley, Elburg Mountains, N. Persia, 6,500 feet, 9.viii.
1872. W. T. Blanford leg. No. 572.
Blanford never noticed that his types were juvenile birds, and he mixed
up his rupicola of North Persia with S. neumayer tschitscherini of Isfahan and
Shiraz. The type specimen is marked on the label by Blanford : " type-figured
specimen, Ibis, 1873, p. 87," and on the back of the label " specimen-figured
Zoology of Persia."
I united formerly tepfironota and rupicola, but corrected my error, p. xxxii.
of my book. The type specimen has been in the Indian Museum, but was made
a " duplicate " and thus came into our hands.
438. Callisitta azurea expectata Hart. = Callisitta azurea expectata.
Callisitta azurea expectata Hartert, Bull. B.O. Club, xxxv. p. 34 (December 1914— Malay Peninsula).
Type : <J ad., Bukit Frazer, above Semangko Pass, Pahang, Malay Peninsula,
4,000 feet, 10.x. 1909. Ex Coll. Selangor Museum.
439. Dendrophila lilacea Whiteh. = Callisitta frontalis lilacea.
Dendrophila lilacea Whitehead, Bull. B.O. Club, vi. p. 49 (1897— Samar).
Types: (J? ad., Bonga, Samar, 21.vi.1896. John Whitehead leg. Nos.
B 653,654.
440. Sitta corallipes Sharpe = Callisitta frontalis corallipes.
Dendrophila corallipes Sharpe, Ibis, 1888 (Kina Balu, N. Borneo).
Type: $ ad., Kina Balu, 3,000 feet, 26. ii. 1887. John Whitehead leg.
No. 1,030.
441. Sitta frontalis palawana Hart. = Callisitta frontalis palawana.
Sitta frontalis palawana Hartert, Bull. B.O. Club, xvi. p. 11 (1905 — Palawan).
Type : c? ad., Puerto Princesa, Palawan, i. 1898. William Doherty leg.
442. Sitta frontalis saturatior Hart. = Callisitta frontalis saturatior.
Sitta frontalis saturatior Hartert, Nov. Zool. ix. p. 573 (1902 — Gunong Tahan, E. Malay Peninsula).
Type : <J ad„ Gunong Tahan, 4,000 feet, ix. 1901. John Waterstradt Coll.
This is a very distinct form, inhabiting the mountains of the Malay Peninsula.
Gunong Tahan, Semangko Pass, etc.
443. Neositta magnirostris Ingram = Neositta striata magniroslris.
Neositta striata magniroslris Ingram, Bull. B.O. Club, xxi. p. 99 (1908 — Inkerman, North Queensland).
Type : <2, Inkerman Station, 14. hi. 1907. W. Stalker leg.
NoVITATES ZOOLOGIOAE XXVII. 1920. 441
PARIDAE.
444. Regulus regulus anglorum Hart. = Regulus regulus anglorum.
Regulus regulus anglorum Hartert, Bull. B.O. Club, xvi. p. 11 (" Great Britain, Isle of Wight, Scotland,
and Ireland ").
Type : £ ad., Tring Park, 31.x. 1900. Ernst Hartert leg.
445. Regulus regulus interni Hart. = Regulus regulus interni.
Regulus regulus interni Hartert, xvi. p. 45 ( 1906 — Corsica and Sardinia).
Type: <J ad., Sassari, Sardinia, 6.H.1904. (Purchased from Squilloni.)
446. Leptopoecile sopliiae deserticola Hart. = Leptopoecile sophiae deserticola.
Leptopoecile sophiae deserticola Hartert, Vbg. pal. Fauna, i. p. 401 (1907 — " Gebirge am Siidrande
des Tarim — Beckens und der Wiiste Gobi ").
Type : <J, Kara-Sai, East Turkestan, xi.1889. Pewzow leg.
447. Anthoscopus ansorgei Hart. = Anthoscopus ansorgei.
Anlhoscopus ansorgei Hartert, Bull. B.O. Club, xv. p. 74 (1905 — Benguella).
Type : <$ ad., Mangonga River, Benguella, 15.xii. 1904. W. J. Ansorge leg.
No. 912.
? 448. Anthoscopus sharpei Hart. = 1 Anthoscopus caroli sylviella Rchw.
Anthoscopus sharpei Hartert, Bull. B.O. Club, xv. p. 75 (1905 — Usambiro).
Type : 9, Usambiro, south of Victoria Nyanza, 8.ix. 1889. Emin Pasha leg.
No. 336.
A. sylviella had been described a year before by Reichenow, Orn. Monatsber.
xii. p. 27, 1904, from Usafua, north of Lake Nyassa. It is still doubtful if it is
the same.
449. Aegithalus musculus Hartl. = Anthoscopus musculus.
Aegitlialus musculus Hartlaub, Orn. Centralblatt, vii. p. 91 (1882 — Lad6).
Type: Lado, 8. hi. 1881. Emin Pasha leg.
(I have here used the name, Anthoscopus for the African Penduline Tits,
which have a much longer first primary and comparatively shorter tail than the
palaearctic forms, though I hardly consider the separation necessary. The
oldest generic name is Remiz Jarocki, 1821, monotype pendulinus \)
450. Anthoscopus pendulinus persimilis Hart. = Remiz pendulinus persimilis.
'.thoscopus pendulinus persimilis Hartert, Nov. Zool. 1918. p. 308 (Eregli in S.E. Asia Minor to Lake
Urmia and Lenkovan).
Type : <J ad., Eregli, south-eastern Asia Minor, 8. v. 1908. P. Urmos leg.
442 NOVTTATES ZOOLOGJCAE XXVII. 1920.
450 a. Anthoscopus rothschildi Neum. = Anthoscopus rothsckildi.
Anthoscopus rothschildi Neumann, Journ. f. Orn. 1907. p. 597 (One specimen from Simba, British
East Africa).
Type : $, Simba, 18.i. 1906. Coll. Maurice de Rothschild. No. 55.
The collection made by Dr. van Someren seems to confirm the distinctness
of this form, but the material of the genus is so far too insufficient to say which
are subspecies and which species. Probably rothschildi will in the end be treated
as a subspecies of another form.
451. Aegithalos caudatus pyrenaicus Hart. = Aegithalos caudatus pyrenaicus.
Description : Nov. Zool. sxv. p. 429 (1918 — Central Pyrenees) ; name : Bull. B.O. Club, xxxix.
p. 40 (1918).
Type : <J ad., Reine Hortense near Cauterets, Central Pyrenees, 1,400 m.,
22.iii.1907. J. Mousques leg.
452. Aegithalos caudatus italiae Jourdain = Aegithalos caudatus italiae.
Aegithalos caudatus italiae Jourdain, Bull. B.O. Club, xxvii. p. 39 (1910 — Italy).
Type : £ ad., Cremona, ix. 1907. Ferragni leg.
(Hilgert, in Kat. Coll. Erlanger, p. 177, 1908, first called attention to this
form, saying that some specimens from Cremona were neither A. c. roseus nor
irbii, while others he thought were irbii, of which, however, he had never seen
a specimen.)
453. Paras lugubris anatoliae Hart. = Parus lugubris anatoliae.
Par-us lugubris anatoliae Hartert, Vog. pal. Fauna, p. 368 (1905 — ■" Kleinasien : bergbewohnend ").
Type : " Ahoory," Asia Minor, 5,000 feet, 6.iv. 1874. H. J. Elwes leg.
(A specimen of Parus lugubris which seemed to me to agree perfectly with
anatoliae was purchased by Giglioli at Nice and introduced into the Italian Fauna
by Giglioli. It was purchased from Messrs. Gal, who palmed off several foreign
species to Giglioli, who accepted them without criticism ; probably all were
obtained elsewhere, as Gal jreres were notoriously unreliable ; nor does Nice
belong to Italy, but our late friend considered all countries as Italian which he
thought should be Italian, including Dalmatia, Nice, etc.)
454. Paras caeruleus ogliastrae Hart. = Parus caeruleus ogliastrae.
Parus caeruleus ogliastrae Hartert, Vog. pal. Fauna, p. 349 (1905 — Sardinia and Corsica).
Type : (J ad., Lanusei, district of Ogliastra, eastern Sardinia, 2.ii. 1902.
455. Paras sarawacensis Slater = Parus major sarawacensis.
Parus cinerascens (nee Vieillot) Slater, Ibis, 1885. pp. 121-123. pi. iv. (Bungal Mts., Sarawak, N.
Borneo).
Parus sarawacensis Slater, t.c. p. 327 (New name for cinerascens Slat.),
Type : ad., Bungal Mts., Sarawak. VV. A. Harvey leg.
Novitates ZooLoaicAE XXVII. 1920. 443
456. Paras major tibetanus Hart. = Parus major tibetanus.
Partis major tibetanus Hartert, Vog. pal. Fauna, p. 346 (1905 — Tsongpo Valley, in eastern Tibet).
Type: <J ad., Chaksam, Tsongpo Valley, 25. ix. 1904. Colonel Waddell leg.
(Received from H. E. Dresser.)
457. Paras major caschmirensis Hart. = Parus major caschmirensis.
Parus major caschmirensis Hartert, Vog. pal. Fauna, p. 345 ( 1905 — Mts. of Kashmir).
Type: ad., Gilgit, 26. xi. 1878. J. Scully leg. No 2,618.
458. Paras major planoram Hart. = Parus major planorum.
Parus major planorum Hartert, Nov. Zool. xii. p. 499 (1905 — Southern Punjab).
Type : ad., South Punjab, Lieutenant Cleveland leg.
459. Paras major mahrattarum Hart. = Parus major mahrattarum.
Parus major mahrattarum Hartert, Nov. Zool. xii. p. 499 (1905 — South India and Ceylon).
Type: $ ad., Ceylon, 1.x. 1868. E. Holdsworth leg. No. 182.
460. Paras major hainanus Hart. = Parus major hainanus.
Parus major hainanus Hartert, Nov. Zool. xii. p. 499 (1905 — Hainan).
Type : <J ad., Lei Mui Mon, Hainan, 18. xii. 1902. Katsumata leg.
461. Paras major okinawae Hart. = Parus major okinawae.
Parus major okinawae Hartert, Vog. pal. Fauna, p. 346 (1905 — Island of Okinawa, Riu Kiu group).
Type: tJ ad., Okinawa, 14.iii. 1902. N. C. Rothschild, F. Gayner and
A. W. Waters leg. No. 61.
462. Paras major terraesanctae Hart. = Parus major terraesanctae.
Parus major terraesanctae Hartert, Vog. pal. Fauna, i. p. xxxii. (1910 — Palestine).
Type : <$ ad., Jerusalem, 2.ii. 1899. ! Bacher leg. No. 179 (not 177).
463. Parus montanus kleinschmidti Hellm. = Parus atricapillus kleinschmidti.
Parus montanus kleinschmidti Hellmayr, Orn. Jahrb. 1900. p. 212 (England).
Type: $ ad., Coalfall Wood, Finchley, near London, N., 22. ix. 1897.
W. Burton leg.
464. Paras palustris hellmayri Bianchi — Parus palustris hellmayri.
Parus palustris hellmayri Bianchi, Annuaire Mus. Zool. St. Petersbourg, vii. p. 236 (1902 — Based on
" Parus sp. nov." Kleinschmidt, Orn. Jahrb. viii. p. 77, 1897, Peking).
Type : <J juv., Peking, v. 1885.
Kleinschmidt and I wisely hesitated to name this form from the material
available, though it appears to be quite distinct. (Cf. also Hartert, Vog. pal.
Fauna, p. 375 ; Hellmayr, Genera Avium, part 18, pp. 12, 34.)
444 NoVITATES ZOOLOQICAE XXVII. 1920.
465. Parus ater insularis Hellm. = Parus ater insularis.
Pants ater insularis Hellmayr, Orn. Jahrb. xiii. p. 36 (1902 — Japan).
Type: <J ad., Suruga, island of Hondo. From Alan Owston.
466. Parus niger lacuum Neum. = Parus niger lacuum.
Parus niger lacuum Neumann, Journ.f. Orn. 1906. p. 260 (Suksuki River, South Ethiopia).
Type : $ ad., Suksuki River, 27. xi. 1900. Oscar Newmann leg.
t 467. Micropus Nehrkorni Bias. = Penthornis tessacourbe Scop.
Muscicapa Tessacmtrbe Scopoli, Del. Florae et Faunae Insubr. ii. p. 95 (1786 — Based on the " Gobe-
mouche noir de l'isle de Luzon " of Sonnerat, Vog. Nouv. Guinke, p. 59, pi. 27. fig. 2, which, how-
ever, must have come from Mindanao !).
Muscicapa luzoniensis Gmelin, Syst. Nat. i. 2. p. 942 (1789 — Based on the same).
Micropus Nehrkorni Blasius, Journ. f. Orn. 1890. p. 147 (Mindanao).
Type: £ in very worn plumage, Davao, Mindanao, S.viii.1889. Dr. C.
Platen leg. (Exchanged from Adolf Nehrkorn.)
LANIIDAE.
468. Pachycare flavogrisea subaurantia R. & H. = Pachycare flavogrisea
subaurantia.
Pachycare flavogrisea subaurantia Rothschild & Hartert, Orn. Monatsher. xix. p. 157 (1911 —
" Schneegebirge im mittleren Neuguinea ").
Type : <J ad., Snow Mountains, Dutch New Guinea, 22.x. 1910. A. S. Meek
Coll. No. 4,873.
469. Poecilodryas cinereiceps Hart. = Eopsaltria cinereiceps.
Poecilodryas cinereiceps Hartert, Nov. Zool. xii. p. 231 (1905 — West Australia : island near Hampton
Harbour, Derby, N.W. Cape).
Type: <J ad., island near Hampton Harbour, W. Australia, 13.vii.1901.
J. T. Tunney leg. No. R 193.
(Mathews, in his latest list, makes cinereiceps a subspecies of E. leucura ;
this may be correct, but I prefer to await his final judgment.)
470. Pachycephala fortis trobriandi Hart. = Pachycephala, fortis trobriandi.
Pachycephala fortis trobriandi Hartert, Nov. Zool. 1896. p. 236 (Trobriand Islands).
Type : <J ad., Kiriwina, Trobriand Islands, east of British New Guinea,
16.iii. 1895. A. S. Meek Coll. No. 7.
471. Pachycephala par Hart. = Pachycephala par par.
Pachycephala par Hartert, Nov. Zool. 1904. p. 211 (Romah Island, N.E. of Timor).
Type : J ad., Romah, 9.viii. 1902. Heinr. Kuhn leg. No. 5,339.
NOVITATES ZOOLOG1CAE XXVII. 1920. 445
472. Pachycephala par compar Hart. = Pachycephala par compar.
Pachycephala par compar Hartert, Nov. Zool. si. p. 212 (1904 — Letti and Moa).
Type : <J ad., Letti Island, 4.xi.l902. Heinr. Kiihn leg. No 6.033.
473. Pachycephala tenebrosa Rothsch. = Pachycephala tenebrosa.
Pachycephala tenebrosa Rothschild, Bull. B.O. Club, xxix. p. 20 (1911 — Mt. Goliath, Central Eastern
Dutch New Guinea.).
Type : cJ ad., Mt. Goliath (eastern part of " Snow Mountains "), 15. ii. 1911.
A. S. Meek Coll. No. 5,394.
474. Pachycephala nudigula Hart. = Pachycephala nudigula.
Pachycephala nudigula Hartert, Nov. Zool. iv. p. 171 (1897 — " Flores meridionalis " ) ; t.c. pi. iii.
fig. 3.
Type : $ ad., South Flores, above 3,000 feet, October 1896. Alfred Everett
leg.
(Homo furore generico : hie Rhodus, hie salta !)
475. Pachycephala rufinucha Scl. = Pachycephala rufinucha rufinucha.
Pachycephala rufinucha Sclater, Proc. Zool. Soc. London, 1873. p. 692 (" Atain apud montes Papuanos
Arfak ").
Type or cotype : $ ad., Hatam, Arfak Peninsula, ix.1872. Luigi Maria
d'Albertis leg. No. 469. (Specimen a of Salvadori's list in Om. Pap. ii. p. 225,
marked by Sclater " Pachycephala rufinucha Scl. sp. nov." and by Salvadori
" Tipo ! ")
476. Pachycephala gamblei Rothsch. = Pachycephala rufinucha gamblei.
Pachycephala gamblei Rothschild, Bull. B.O. Club, vii. p. xxii. (1897 — Mt. Cameron, Owen Stanley
Mts., British New Guinea).
Type : " $ " ad. (? $), Mt. Cameron, 5,000 feet. A. S. Anthony leg.
477. Pachycephala nieeki Hart. = Pachycephala leucogaster meeki.
Pachycephala meeki Hartert, Bull. B.O. Club, viii. p. xv. (1898 — Rossel Island, Louisiade group).
Type : $ ad., Rossel Island, 27. i. 1898. Albert S. Meek leg. No. 1,299.
478. Pachycephala tianduana Hart. = Pachycephala leucogaster tianduana.
Pachycephala tianduana Hartert, Bull. B.O. Club, xi. p. 53 (1901 — " Tiandu, west of the Key
Islands ").
Type : <J, Tiandu, 19.xii.1900. Heinr. Kiihn leg. No. a.
479. Pachycephala johni Hart. = Pachycephala johni.
Pachycephala johni Hartert, Nov. Zool. 1903. p. 12 (Obi Major, Moluccas).
Type : (J ad., Obi Major, 25. iii. 1902. John Waterstradt leg. No. O 129.
29
446 NOVITATES ZOOLOGICAE XXVII. 1920.
480. Pachycephala kuehni Hart. = Pachycephala griseonota kuehni.
Pachycephala kuehni Hartert, Bull. B.O. Club, viii. p. xiv. (1898— Little Key Islands).
Type : <J Tual, Little Key, 11. xi. 1897. Heinr. Kiihn leg. No. 281.
481. Pachycephala examinata Hart. = Pachycephala griseonota examinata.
Pachycephala examinata Hartert, Bull. B.O. Club, viii. p. xiv. (1898— Buru).
Type : <J ad., Kayeli, Buru, iii. 1897. William Doherty leg.
482. Pachycephala moroka R. & H. = Pachycephala morohi.
Pachycephala moroka Rothschild & Hartert, Nov. Zool. 1903. p. 106 (Moroka, S.E. New Guinea).
Type : ad., Moroka district, British New Guinea, 3—6,000 feet. (Purchased
from Messrs. Mcllwraith, McEacharn & Co., 1898.)
f 483. Pachycephala peninsulae Hart. = Pachycephala griseiceps inornata.
Eo2>sallria 1 inornata Ramsay, Proc. Zool. Soc. London, 1874. p. 604 (Rockingham Bay and Endeavour
River, North Queensland).
Pachycephala peninsulae Hartert, Bull. B.O. Club, viii. p. xxxiii. (1899 — Cape York, North Queens-
land).
Type : <J, Cape York, 29.vii.1898. Eichhorn leg. No. 2,041 of the Meek
collections.
There seems to me no doubt that my " peninsulae " is a synonym of Ramsay's
inornata, though Mathews, List of B. Australia, p. 181 (1913), keeps them distinct
as two different subspecies. He there splits our Pachycephala up into about
half a dozen genera.
484. Pachycephala alberti Hart. = Pachycephala griseiceps alberti.
Pachycephala griseiceps alberti Hartert, Bull. B.O. Club, viii. p. ix. (1898 — Sudest Island, Louisiade
group).
Type : <$ ad., Sudest Island, 8.iv. 1898. A. S. Meek Coll. No. 1,693.
485. Pachycephala orpheus wetterensis Hellm. =Pachycephala orpheus
u-rtterensis.
Pachycephala orpheus wetterensis Hellmayr, Zoohgie von Timor, i. p. 35 (1914 — Wetter).
Type : 9 ad., Wetter Island, 9.x. 1902. Heinr. Kiihn leg. No. 5,725.
f 486. Hyloterpe whiteheadi Sharpe = Pach yet phala {Hyloterpe) grisola plateni.
Hyloterpe Plateni Blasius. Braunschweig. Am. Xc>. .">:.'. p. 467 (1. iii. 1888 — Palawan); Ornis, 1888,
p. 311.
Hyloterpe whiteheadi Sharpe, Ibis, 1888. p. 198 (April 1S88 — Palawan).
(About the dates of these names cf. under No. 378.)
Type: 9 ad., Taguso, Palawan, 21 .vii. 1887. John Whitehead leg. No.
1,587.
NOVITATES ZOOLOGICAE XXVII. 1920. 447
487. Hyloterpe hypoxantha Sharpe = Pachycephala (Hyloterpe) hypoxanlha.
Hyloterpe hypoxanilm Sharpe, Ihis, 1887. p. 451 (Kina Balu, Borneo).
Type: g ad., Kina Balu, 3,000 feet, 25. ii. 1887. John Whitehead leg.
No. 1,018.
488. Pachycephala grisola secedens Stres. = Pachycephala (Hyloterpe) grisola
secedens.
Pachycephala grisola secedens Stresemann, Nov. Zool. xx. p. 355 (1913 — Sirhassen Island).
Type : $ ad., Sirhassen Island, eastern Natuna group, 21. ix. 1893. Alfred
Everett leg.
The distribution of this form is curious. A specimen from Great Redang
Island, east of Kelantan, Malay Peninsula, l.ix.1910. C. Boden Kloss leg.,
belongs also clearly to secedens.
489. Hyloterpe Homeyeri Bias. = Pachycephala (Hyloterpe) homeyeri.
Hyloterpe Homeyeri Wilh. Blasius, Journ. f. Orn. 1890. p. 143 (Descr. from one female from Yol6
Sulu).
Type: $, Yolo, Sulu Islands, 15. v. 1887. Dr. Platen leg. (Exchanged
from A. Nehrkorn.)
490. Pachycephala schlegeli obscurior Hart. = Pachycephala schlegeli obscurior.
Pachycephala schlegeli obscurior Hartert, Nov. Zool. iii. p. 15 (1896 — Owen Stanley Mts., British
New Guinea).
Type : (J ad., Eafa district, between Mts. Alexander and Bellamy, 5 — 6,000
feet, October 1895. A. S. Anthony leg.
(Synonym : Pack, sororcvla de Vis 1897, p. 380, described from a$, supposed
to be (J, from spirits !)
491. Pachycephala melanonota Hart. = Pachyceplmla melanonota.
Pachycephala melanonota Hartert, Bull. B.O. Club, xxi. p. 106 (1908 — Vella Lavella, Solomon Islands).
Type: $ ad., Vella Lavella, Central Solomon Islands, 23. ii. 1908. A. S.
Meek Coll. No. 3,834.
492. Pachycephala hyperythra reichenowi R. & H. = Pachycephala hyperythra
reichenowi.
Pachycephala hyperythra reichenowi Rothschild & Hartert, Orn. Monatsber. xix. p. 178 (1911 —
" Sattelberg, in Kaiser Wilhelm's Land ").
Type: <J ad., Sattelberg, 21. xi. 1909. Wahnes leg. No. 62.
493. Pachycephala salvadorii Rothsch. = Pachycephala hyperythra salvadorii.
Pachycephala salvadorii Rothschild, Bull. B.O. Club, vii. p. xxii. (1897 — New name for P. sharpii
Salvad. 1896, nee Meyer 1884) ; Nov. Zool. 1903. p. 107.
Type: rj ad., Mt. Cameron, Owen Stanley Range, 13. viii. 1896. A. S.
Anthony leg.
448 Novitates Zoolooicae XXVII. 1920.
494. Pachycephalia contempta Hart. = Pachycephala pectoralis contempta.
Pachycephala contempta Hartert, Bull. B.O. Club, viii. p. xv. (1898 — Loid Howe Island).
Type : J ad., Lord Howe Island. (Purchased from H. H. Travers.)
495. Pachycephala pectoralis goodsoni R. & H. = Pachycephala pectoralis
goodsoni.
Pachycephala pectoralis goodsoni Rothschild & Hartert, Nov. Zool. xxi. p. 296 (1914 — Manus,
Admiralty Islands).
Type: $ ad., Manus, Admiralty Islands, 5.ix.l913. Eichhorn leg. No.
5,970 of the A. S. Meek collections.
496. Pachycephala rosseliana Hart. = Pachycephala pectoralis rosseliana.
Pachycephala rosseliana Hartert, Bull. B.O. Club, viii. p. viii. (1898 — Rossel Island); Nov. Zool.
1899. p. 76.
Type : <J ad., Rossel Island, Louisiade group, 8.ii. 1898. A. S. Meek Coll.
No. 1,405.
497. Pachycephala pectoralis misimae R. & H. = Pachycephala pectoralis
misimae.
Pachycephala pectoralis misimae Rothschild & Hartert, Nov. Zool. xxv. p. 311 (1918 — St. Aignan or
Misima Island, Louisiade group).
Type : <J ad., St. Aignan Island, 29. xi. 1897. A. S. Meek Coll. No. 1,044.
498. Pachycephala melanura buruensis Hart. = Pachycephala pectoralis buruensis.
Pachycephala melanura buruensis Hartert, Bull. B.O. Club, viii. p. xxxii. (1899 — Buru).
Type : <$ ad., " Mt. Mada " (Kapala Madang, Fogha Mts.), Buru, 3,000 feet,
August — September 1898. J. Dumas leg.
499. Pachycephala melanura dammeriana Hart. = Pachycephala pectoralis
' dammeriana.
Pachycephala melanura dammeriana Hartert, Nov. Zool. vii. p. 17 (1900 — Dammer Island).
Type: $ ad., Wulur, Dammer Island, 27. xi. 1898. Heinr. Kiihn leg.
No. 1,092.
f 500. Pachycephala melanura tepa Hart. = Pachycephala pectoralis sharpei.
Pachycephala Sharpei A. B. Meyer, Sitzungsber. & Abh. Ges. Isis Dresden 1884, Abh. p. 36 (1885 —
Babber !).
Pachycephala melanura tepa Hartert, Nov. Zool. xiii. p. 299 (1906 — Babber !).
Type : £ ad., Tepa, Babber, 15. ix. 1905. Heinr. Kiihn leg. No. 6,644 a.
501. Pachycephala melanura arthuri Hart. = Pachycephala pectoralis arthuri.
Pachycephala melanura arthuri Hartert, Nov. Zool. xiii. p. 299 (1906 — Wetter Island).
Type: (J ad., Wetter, 14. ix. 1902. Heinr. Kiihn leg. No. 5,498.
Novitates Zoolooicae XXVII. 1920. 449
502. Pachycephalia everetti Hart. = Pachycephala pectoralis everetti.
Pachycephala everetti Hartert, Nov. Zool. hi. p. 170 (1896 — Djampea Island, south of Celebes).
Type : <J ad., Djampea, xii.1895. Alfr. Everett leg.
503. Pachycephala fulviventris Hart. = Pachycephala pectoralis fulviventris.
Pachycephala fulvivenlris Hartert, Bull. B.O. Club, v. p. xlvii. (1896 — Sumba Island).
Type : $ ad., Sumba, ii . 1896. William Doherty leg.
504. Pachycephala pectoralis alfurorum Stres. = Pachycephala pectoralis
alfurorum.
Pachycephala pectoralis alfurorum Stresemann, Nov. Zool. xxi. p. 132 (1914 — Cerara).
Type : <J ad., Gunong Sofia, Ceram, 4,800 feet, 14. vi. 1911. Erwin Strese-
mann leg. No. 614.
505. Nilaus afer erythreae Neum. = Nilaus afer erythreae.
Nilaus afer erythreae Neumann, Journ.f. Orn. 1907, p. 361 (" Nord-Abyssinien ").
Type : £ ad., Ailet, Erythraea, 5.iv.l903. G. Schrader leg.
This form is very closely allied to N. afer afer (terra typica Senegal), but
recognizable, and in my opinion chiefly by the darker chestnut lateral stripes.
506. Nilaus afer hilgerti Neum. = Nilaus afer hilgerti.
Nilaus afer hilgerti Neumann, Journ.f. Orn. 1907. p. 362 (" Hauaschgebiet von Schoa, nach Siiden
bis zum Zuai-See nachgewiesen ").
Type : (J ad., Kassam River, Hawash region, 24. vi. 1903. Zaphiro leg.
[507. Nilaus minor Sharpe = Nilaus afer minor.
Nilaus minor Sharpe, Proc. Zool. Soc. London, 1895. p. 479 (" Somaliland," Milmil and other
localities).
Type : according to Neumann, Journ. f. Orn. 1907, p. 362 : $ ad., Milmil,
2.vii.l894. Dr. Donaldson Smith leg., but this can only be a paratype, as the
J ad. from Okoto, 8.ix. 1894, in the British Museum is there marked as the type
by the author.]
(?) t 508. Telophonus senegalus pallidus Neum. = Harpolestes * senegalus
senegalus.
Telophonus senegalus pallidus Neumann, Journ. f. Orn. 1907. p. 375 (" Ober-Guinea von der Goldkiiste
bis zum Niger ").
Type : cJ ad., Accra, 4.xi. 1897. ■ C. W. Nartey leg.
I must confess that, after a renewed examination of the material in Tring
* There has been a good deal of uncertainty and change of the generic name of the Tchagra-
Shrikes. In the Cat. B. Brit. Mus. viii., Gadow called them Telephonus, and this name has been in
general use before and after. In the V6g. Afr. ii. p. 542, Reichenow introduced the name Pomato-
rhynchus Boie 1826 ; to this I objected because Boie quoted " PomatorhyncMis Horsf." ; Horsfield,
however, never created such a name, but only Potnatorhiniis, and it is evident that Boie merely
amended his spelling, and erroneously placed under that name (which refers to a totally different
group of birds) the Tchagra of Levaillant, of which he did not know that it was a Shrike. In the
Vog. pal. Fauna, p. 452, I then pleaded for the restitution of Telophonus, the original spelling of
450 NOVITATES ZOOLOQICAE XXVII. 1920
and London, it seems to me impossible to separate this race from H. s. senegalus.
The coloration is too variable, and the smaller size not always constant. (See
also Novitates Zoologicae, 1915, p. 259.) (This view is more or less confirmed
by Dr. van Someren's wonderful series, who will soon give us fuller information
about these very difficult forms, and their allies.)
509. Telophonus senegalus rufohiscus Neum. = Harpolestes senegalus
rufojuscus.
Telophonus senegalus rufojuscus Neumann, Journ. f. Orn. 1907. p. 376 (" Nordliches und zentrales
Angola, nach Norden bis ins Congo-Gobiet ").
Type: $ ad., N'Gungo, Northern Baihmdu. Angola, 12.viii. 1901. C.
Hubert Pemberton leg.
This form is very different from T. senegalus senegalus and cannot possibly
be united with it.
510. Harpolestes australis ansorgei Neum. = Harpolestes australis ansorgei.
Harpolesles australis ansorgei Neumann, Bull. B.O. Club, xxiii. p. 53 (1909 — " North Angola ").
Type : <£, Pungo Andongo, 3.vii. 1903. W. J. Ansorge leg. No. 522.
Based on three more or less juvenile birds, but young australis differ in the
same way as old ones. This form is certainly distinct, but it is nearest to H. a.
australis and quite different from souiae.
? | 511. Telophonus australis dohertyi Neum. = Harpolestes australis minor ?
Telophonus australis dohertyi Neumann, Journ. f. Orn. 1907. p. 370 (Escarpment, Kikuyu).
Type : <$ ad., Escarpment, Kikuyu Mts., i. 1901. W. Doherty leg.
The Escarpment birds are all more or less worn or soiled, but it certainly
seems that those from Western Uganda (Bukoba, etc.) are more whitish under-
neath. They cannot, therefore, be united with emini, as Reichenow {Journ. /.
Orn. 19 IS, p. 82) proposed. We have, however, no skins from the terra typica
of minor. Even Dr. van Someren's series does not help us to decide this question.
512. Pelicinius cruentus hilgerti Neum. = Rhodoplioneus cruenttts hilgerti.
Pelicinius cruentus hilgerti Neumann, Orn. Monalsber. 1903, p. 182 (" Nord-und Siidsomaliland ").
Type: Sheikh Husein, W. Somaliland, 23. ix. 1894. Dr. Donaldson Smith
leg. No. 314.
513. Laniarius funebris rothschildi Neum. = Laniarius funebris rothschildi.
Laniarius Junehris rothschildi Neumann, Journ. J. Orn. 1907. p. 595 (" Sud-Athiopien vom Hauasch
bis zum Borana-Land und zum Rudolf-See ").
Type : <j>, Sagan River, Borana, 25. v. 1905. Maurice de Rothschild leg.
Swainson, instead of " Telephonus." Thereupon Reichenow, Orn. Monatsber. 1907, p. 99, pointed
out that Swainson's Telophonus 1837 was obviously only an amended spelling of the same author's
Telophorus of 1831, a name which had been overlooked. I quite agree that, therefore, Telophonus
is no more acceptable than Pomalorhynchus, and use Harpolestes Cab. 1850 for this genus. Sclater
and Mackworth-Praed {Ibis, 1918, p. 636) use the generic " Tsrhagra," but Tschagra of Gray is
obviously only another spelling of Tchagra Lesson. Traitt d'Orn. p. 878, which I take to be a new
name for Laniurius Vicillot, though Lesson included in the same subgenus Levaillant's Tchagra
and a number of other species. |
NOVITATES ZOOLOGICAE XXVII. 1920. 451
514. Pelicinius zeylonus phanus subsp. nov.
Type : ^ ad., Farta Bay, 5 hours south of Benguella Town, 30.x. 1905.
W. J. Ansorge leg.
Seven specimens from Benguella and Mossamedes, collected by the late
W. J. Ansorge and Albert Mocquerys, differ from about a dozen from South Africa
in having the back a little paler green, and the whole yellow portion of the under-
side much lighter, more sulphureous yellow, which is specially striking on the
throat, abdomen, and under tail-coverts. There is no appreciable difference in
size. I therefore name the Benguella-Mossamedes form Pelicinius zeylonus
phanus, type as above.
Probably a third form inhabits Namaqualand, as a male and female collected
by C. B. Grant in May and July 1903, at an elevation of 3, 104 feet, appear to have
the flanks and sides of breast much more widely ashy grey, and are a little smaller.
More material will probably lead to the establishment of a third form.
(I am using reluctantly the generic name Pelicinius, while I separate
cruentus and its subspecies as Rhodophoneus. In this I am following Sharpe's
Hand-list, iv. pp. 292, 293, without wishing to discuss the genera of these shrikes,
of which perhaps too many are now being used. )
515. Laniarius rubiginosus rudolfi Hart. = Chlorophoneus rubiginosus rudolfi.
Laniarius rubiginosus rudolfi Hartert, Bull. B.O. Club, xxiii. p. 10 (1908— forest west of Lake Albert
Edward).
Type : $ ad., Primeval forest 90 kilometres west of Lake Albert Edward,
7.ii.l90S. Rudolf Grauer leg. No. 1,979.
516. Laniarius dohertyi Rothsch. = Chlorophoneus dohertyi.
Laniarius dohertyi Rothschild, Bull. B.O. Cluh, xi. p. 52 (1901 — Escarpment, Kikuyu Mts., B. E.
Africa).
Type: J ad., Escarpment, Kikuyu Mts., 8,000 feet, xii.1900. William
Doherty leg.
t 517. Laniarius graueri Hart. = Chlorophoneus melamprosopus reichenowi.
Laniarius graueri Hartert, Bull. B.O. Club, xxiii. p. 9 (1908— Forest west of Lake Albert Edward).
Type: <$ ad., Primeval forest, 90 km. west of Lake Edward, 1,600 m.,
14. ii. 1908. Rudolf Grauer leg. No. 2,039.
I am now convinced that my L. graueri is the same as L. m. reichenowi — if
indeed the latter is separable from true melamprosopus !
518. Lanius gubernator Hartl. = Lanius gubernator.
Lanius gubernator Hartlaub, Orn. CentraUil. 1882. p. 91 (No exact locality, diagnosis of S !) ; Journ.
f. Orn. 1882. p. 323. pi. i. fig. 2 (Langomeri).
Type : cj ad., Langomeri, Emin Pasha leg.
There is no doubt that the adult male must be looked upon as the real type
of L. gubernator, but the notes in Journ. f. Orn. 1882, pp. 323, 324, are somewhat
confused. The first diagnosis in the Ornithologische Centralblatt is that of the
adult male only. Curiously enough, in the Journ. f. Orn. also the male only is
. 452 NOVITATES ZOOLOOIOAE XXVII. 1920.
described, though at the end of the description, p. 324, stands " $ ad." On the
plate the male only is figured, and this agrees with the lettering of the plate, but
on p. 323 it is erroneously said that the figure is that of the female ! On p. 324
Hartlaub wrote that four specimens were obtained at Langomeri, an adult male
and female, and two young birds. We have all these four in the Tring Museum,
and the sexes are correctly stated on the labels. The female, which has no black
frontal line, was not described by Hartlaub at all, though he says, " Zunachst
erhielten wir nur das ausgefarbbe Weibchen " ! I suppose he meant to say
" Mannchen " instead of " Weibchen," and that the " $ ad. " at the end of the
description of the male means that it was the author's intention to describe the
$ as well, which, however, he did not do.
f 519. Lanius excubitorius intercedens Neum. = Lanius excubitorius
excubitorius.
Lanius excuhitorius intercedens Neumann, Journ. f. Om. 1905. p. 228 (" Hauasch-Gebiet, siido-
thiopische Seen, Omo-Gebiet, nach Siiden bis zur Nord-und Ostkiiate des Victoria-Nyansa ").
Type : $ ad., Hauash, south of the Sekwala, 19. xi. 1900. Oscar Neumann
leg. No. 250.
Neumann compared his bird with L. excubitorius princeps. which he thought
were L. excubitorius excubitorius, and his intercedens are typical excubitorius.
520. Lanius antinorii mauritii Neum. = Lanius antinorii mauritii.
Lanius antinorii mauritii Neumann, Journ. f. Orn. 1907. p. 595 (Koroli Mountains, West Somaliland).
Type and unique specimen : <J ad., Kovoli Mts., 18. iv. 1905. Maurice de
Rothschild leg.
It was daring to describe this form from one specimen, and it is desirable to
have a series to confirm its validity, but the differences pointed out by Neumann
are very obvious, so that the new subspecies appears to be very distinct.
521. Malaconotus interpositus Hart. = Malaconotus poliocephalus interpositus.
Malaconotus interpositus Hartert, Bull. B.O. Club, xxix. p. 36 (1911 — North-west of Lake Tangan-
yika).
Type: S ad., 40 km. west of Baraka, 5. i. 1909. Rudolf Grauer leg.
No. 4,019.
This form is very closely allied to M . poliocephalus poliocephalus from Sene-
gambia to Nigeria, and must be confirmed by further research.
522. Sigmodus caniceps harterti Neum. = Sigmodus caniceps harterti.
Sigmodus caniceps harterti Neumann, xxi. p. 70 (1908 — Southern Nigeria).
Type: cJ ad., Degama, Southern Nigeria, 15.iii. 1902. W. J. Ansorge leg.
No. 220.
(?) 523. Prionops cristata omoensis Neum. = (?) Prionops cristata cristata.
Prionops cristata omoensis Neumann, Journ.}. Orn. 1905. p. 216 (" Hussgebiet des Omo ").
Type j S Omo, between Malo and Kosha, 23. ii. 1901. Oscar Neumann
leg. No. 929.
NoVITATES ZOOLOGIOAE XXVII. 1920. 453
The nape is much darker in one specimen, and a specimen from Salamona
(G. Schrader leg), as well as another from Mulu (Saphiro leg.), have it quite as
dark as the one of Neumann's two specimens. The wing of one is shorter, that
of the other not. In no case were two specimens sufficient to establish such a
closely allied subspecies, and we must await further material from the Omo,
whenever that may come, to establish Neumann's " omoensis." (A series collected
by Dr. van Someren seems to confirm omoensis, but we shall hear more about
this from him before long.)
524. Pinarolestes megarhyncha despeetus R. & H. = Pinarohstes megarhynchus
despectus.
Pinarolestes megarhynchus despectus Rothschild & .Hartert, Nov. Zool. 1903. p. 100 (British New
Guinea).
Type : $, Milne Bay, South-Eastern British New Guinea, 14. ii. 1899. A. S.
Meek Coll. No. 2,323.
525. Colluricincla brunnea tachycrypta R. & H. = Colluricincla brunnea tachy-
crypta.
Colluricincla brunnea tachycrypta Rothschild & Hartert, Nov. Zool. xxii. p. 60 (1915 — Milne Bay,
South-Eastern Papua).
Type : (J ad., Milne Bay, 19. iv. 1899. A. S. Meek Coll. No. 2,484.
526. Colluricincla woodwardi Hart. = Colluricincla woodwardi.
Colluricincla woodwardi Hartert, Nov. Zool. xii. p. 228 (1905 — Granite hills near South Alligator
River, Northern Territory).
Type : cj ad., ten miles east of South Alligator River, 15.viii. 1903. J. T.
Tunney leg. No. 1,545.
527. Pitohui meeki R. & H. = Pitohui meeki.
Pitohui meeki Rothschild & Hartert, Nov. Zool. xx. p. 507 (1913 — Mount Goliath, eistem portion
of " Snow Mountains," in Dutch New Guinea).
Type : $, Mt. Goliath, 7 . ii . 1911. A. S. Meek Coll. No. 5,321.
This species — possibly a subspecies of nigrescens — was described from a
single female. The male has been described by Ogilvie-Grant, Jubilee Suppl. II.
of Ibis, 1915, p. 105.
528. Rhectes ferrugineus brevipennis Hart. = Pitohui ferrugineus brevipennis.
Rhectes ferrugineus brevipennis Hartert, Nov. Zool. 1896. p. 354 (Aru Islands).
Type: ad., Wannambai, Aru Islands, 25. vi. 1896. Cayley Webster leg.
No. 217.
529. Pitohui meyeri R. & H. = Pitohui meyeri.
ischild & Hartert, Nov. Zool. x. p. 96 (1903—" Hab. In Noi
?ana Mera ").
Type: <J, Takar, October 1896. William Doherty leg. No. 1,011.
Pitohui meyeri Rothschild & Hartert, Nov. Zool. x. p. 96 (1903 — " Hab. In Nova Guinea septentr.
prope Takar, Tana Mera ").
454 NnvITATES ZOOLOGICAE XXVII. 1920.
530. Pitohui dohertyi R. & H. = Pitohui dohertyi.
Pilohui dohertyi Rothschild & Hartert, Nov. Zool. x. p. 95 (1903 — Ron Island, in Geclvink Bay).
Type : <J ad., Ron Island, vi. 1897. William Doherty leg. No. 969.
531. Pitohui dichrous monticola Rothsch. = Pitohui dichrous moniicola.
Pitohui dichrous monticola Rothschild, Bull. B.O. Club, xiv. p. 79 (1904 — Upper Aroa River).
Type: <S ad., Upper Aroa River, British New Guinea, 27. i. 1903. A. S.
Meek Coll. No. A 124.
Mr. W. R. Ogilvie-Grant (Ibis, Jubilee Suppl. II., 1915, pp. 99, 100) mentions
three specimens from the Utakwa River, 2,900 feet, which agree with specimens
from the Aroa River and other places in British New Guinea. From this he
concludes that monticola " must be added to the synonymy " of P. dichrous.
because these specimens " must be typical examples of P. dichrous, the type of
which was procured by S. Miiller at Lobo, Triton Bay." This conclusion is rash,
and I do not agree with it. We have in the Tring Museum 2:2 skins from Arfak,
Humboldt Bay, Simbang, and Sattelberg. which are perfectly alike, and which
we took to be typical dichrous, while 10 specimens from the mountains of British
New Guinea are at a glance distinguished by their paler colour. Therefore,
Lord Rothschild very logically separated the latter as P. dichrous monticola.
We had of course not seen specimens from the Snow Mountains, and it does not
follow that they " must be. " typical examples of dichrous, as they came from the
mountains and Salomon Muller's were collected near the coast, in the low country ;
moreover, in many cases, forms from the Utakwa River agree more with those
from South-Eastern Papua, while many Lobo-Bay ones are exactly like those
from Arfak. Until, therefore, the type from Lobo in the Leyden Museum is
carefully compared with specimens from Arfak and the mountains of British
New Guinea, we have not to alter the present state, and must admit monticola.
Should, against all expectations, the Lobo type be like our monticola, then the
darker northern form from Arfak, Humboldt Bay, and Simbang must receive
a new name !
532. Abbotornis schistocercus Neum. = Abbotornis schistocercus.
Ahhotornis schistocercus Neumann, Bull. B.O. Club, xxiii. p. 11 (1908 — " West Central Madagascar ").
Type : <$ ad., " C. O. Madagascar," which, I am now convinced, must mean
West Colst (not West Central) Madagascar. (Bought with others from a Paris
dealer in 1893.)
533. Gymnorhina tibicen longirostris Hart. — Gymnorhina tibicen longirostris
Milligan.
Gymnorhina tibicen longirostris Hartert, Nov. Zool. xii. p. 230 (1905 — Nullagine, N.W. Australia).
Type: <J ad., Nullagine, 16. iv. 1901. J. T. Tunney leg. No. R 92.
This distinct form retains its fitting name longirostris, though it had been
described two years before by Milligan (Gymnorhina longirostris Milligan, Emu,
iii. p. 96, 1903).
Novitatks Zoolooicae XXVII. 1920. 455
f 534. Cracticus quoyi tunneyi Hart. = Cracticus quoyi spaldingi.
Cracticus spaldingi Masters, Proc. Linn. Soc. N.S. Wales, ii. p. 271 (1877 — Port Darwin, Northern
Territory).
Cracticus quoyi tunneyi Hartert, Nov. Zool. xii. p. 228 (1905 — Alligator River, Northern Territory).
Type : ^ ad., Alligator River, Northern Territory, 25 . ix . 1903. J. T. Tunney
leg. No. 1,603.
ARTAMIDAE.
f 535. Artamus Ieucorhynchus parvirostris Hart. = Artamus leucorhynchus
leucopygialis.
Artamus leucorhynchus parvirostris Hartert, Nov. Zool. vi. p. 424 (1899 — Cape York, North Queens-
land).
{Artamus leucopygialis Gould, Proc. Zool. Soc. London, 1842. p. 17 [New South Wales].)
Type: $ ad., Cape York, 5.vii.l898. Eichhorn leg. A. S. Meek coll.
No. 1,876.
(Other synonyms are harterti Math, and melvillensis Math.)
536. Artamus leucorhynchus humei Stres. = Artamus leucorhynchus humei.
Artamus leucorhynchus humei Stresemann, Nov. Zool. xx. p. 291 (1913 — " Andamanen, einschliesslich
der Grossen und Kleinen Kokos-Insel ").
Type : ? ad., Go-bang, South Andamans, October 1897. A. L. Butler leg.
f 537. Artamus phoeus Ingram = Artamus superciliosus.
Artamus phoeus Ingram, Bull. B.O. Club, xvi. p. 115 (1906— Alexandria station, Norther.: Territory).
Type : <J ad., Alexandria, 28. v. 1905. W. Stalker leg. No. 626.
f 538. Artamus gracilis Ingram = Artamus personal/is.
Artamus gracilis Ingram, Bull. B.O. Club, xvi. p. 115 (1906 — Alexandria station, Northern Territory).
Type: <J ad., Alexandria, 16. i. 1906. W. Stalker leg.
Mathews, List B. Austr. pp. 234, 235, separated the three supposed species
of Ingram as subspecies, but he now agrees with me (March 1919, in litt.) that
" all three are undoubtedly synonyms."
f 539. Artamus rlorenciae Ingram = Artamus cinereus venustus.
Artamus fiorenciae Ingram, Bull. B.O. Club, xvi. p. 115 (1906— Alexandria station, Northern
Territory).
TyPe : <J (apparently not adult), Upper Playford, Northern Territory,
20.iii.1906. W. Stalker leg.
(Cf. Hellmayr, Novitates Zoologicae, 1916, pp. 100, 101.)
VIREONIDAE
540. Vireo josephae mirandae Hart. = Vireo josephae mirandae.
Vireo josephae mirandae Hartert, Bull. B.O. Club, xxxvii. p. 32 (February 1917— Cerro del Avila,
north of Caracas, 2,000 m.).
Type : <^ ad., Galiparo, Cerro del Avila, 2,000 m.. 15. xii. 1913. Samuel M.
Klages leg. No. 1,178.
456 Novitates Zooi-ooicae XXVII. 1920.
541. Hylophilus thoracicus griseiventris Berl. & Hart. = Hylophilus thoracicus
griseiventris.
Hylophilus thoracicus griseiventris Berlepsch & Hartert, Nov. Zool. ix. p. 11 (1902 — Orinoco).
Type : $ ad., Suapure, Orinoco. 11 . ii . 1899. Samuel M. Klages leg.
(In contradiction to the International Rules of Nomenclature, Hylophilus
has been replaced by " Pachysilvia," because of an earlier Hylophila of Hiibner.
Such unnecessary and unauthorized changes do more harm to uniform nomen-
clature than anything else, and it is a great pity that they have been adopted
by the A.O.U.)
542. Pachysylvia aurantiifrons saturata Hellm. = Hylophilus aurantiifrons
saturatus.
Pachysylvia aurantiifrons saturata Hellmayr, Nov. Zool. xiii. p. 12 (1906 — Cumana, North Venezuela).
Type : $ ad., Rincon of San Antonio, 18.iii. 1898. Caracciolo leg. No. 978.
543. Hylophilus bulunensis Hart. = Hylophilus ochraceiceps bulunensis.
Hylophilus bulunensis Hartert, Nov. Zool. ix. p. 617 (1902— Bulun, N.W. Ecuador).
Type: <J ad., Bulun, N.W. Ecuador, 160 feet, 6.xii.l900. G. Flemming
leg. No. 253.
544. Vireolanius mikettae Hart. = Vireolanius mikettae (? Subsp. of leucotis).
Vireolanius mikettae Hartert, Bull. B.O. Club, xi. p. 38 (1900— Paramba, N. Ecuador).
Type : <$ ad., Paramba, 3,500 feet, 28.vii. 1899. R. Miketta leg. No. 483.
545. Cyclorhis coibae Hart. = Cyclarhis flaviventris coibae.
Cyclorhis coibae Hartert, Bull. B.O. Club, xii. p. 33 (1901— Coiba Island, off Panama).
Type : cj ad., Coiba Island, 20. iv. 1901. J. H. Batty leg.
MUSCICAPIDAE
(Including " Sylviidae," " Timeliidae" " Turdidae." Cf. Vog. pal. F. p. 469.)
546. Amytornis woodwardi Hart. = Amytornis woodwardi.
Amytornis woodwardi Hartert, Bull. B.O. Club, xvi. p. 30 (1905 — South Alligator River, Northern
Territory).
Type : <J ad., ten miles east of South Alligator River, about 85 miles from
coast, 4.vii.l903. J. T. Tunney leg. No. 1,305.
(Mathews accepts the name Diaphorillas Oberh. 1899, because he considers
Amytornis Stejn. 1885 a nomen nudum. I fail to see how this can be supposed,
as A. textilis is the monotype, and therefore Amytornis must be accepted. I do
not follow the splitting of these closely allied little birds into four genera.)
NOVTTATES ZOOLOQICAE XXVII. 1920. 457
547. Clytomyias insignis oorti R. &. H. = Clytomyias insignis oorti.
Clytomyias insignis oorti Rothschild & Hartert. Nov. Zool. xiv. p. 460 (1907 — head of Aroa River,
British Papua).
Type : " <? " ad., head of Aroa River, 4. v. 1905. A. S. Meek Coll. No.
A 2,171.
548. Todopsis cyanocephalus dohertyi R. & H. = Todopsis cyanocephala
dohertyi.
Todopsis cyanocephalus dohertyi Rothschild & Hartert, Nov. Zool. x. p. 477 (Takar, northern coast
of Dutch New Guinea).
Type : $ ad., Takar, November 1896. William Doherty leg.
(Ogilvie-Grant, Ibis, Jubilee Suppl. II. p. 160, 1915, says that our dohertyi
is " almost certainly identical " with cyanocephala. As all the four females from
Takar have the upperside conspicuously darker chestnut, there is no reason to
think that they are " almost certainly identical," though a large series might
possibly prove this to be the case. Many birds from the northern coast [Takar,
etc.] differ from those of the more western parts of Dutch New Guinea.)
549. Malurus dulcis Math. = Malurus amabilis dulcis (teste Mathews).
Malurus dulcis Mathews, Bull. B.O. Club, xxi. p. 100 (1908— South Alligator River, Northern
Territory).
Types: (J ad., ten miles east of South Alligator River, 9.viii.l903;
$, 4.vii.l903. J. T. Tunney leg. Nos. 1,564, 1,286.
550. Buraesia reichenowi Hartl. = Prinia leucopogon reichenowi.
Burnesia reichenowi Hartlaub, Journ. f. Orn. 1890. p. 151 (Njangalo, Equatorial Africa).
Type: $ ad., Njangalo, 28. iv. 1889. Emin Pasha leg. No. 199.
551. Burnesia bairdi obscura Neum. = Prinia bairdi obscura.
Burnesia bairdi obscura Neumann, Bull. B.O. Club, xxiii. p. 13 (1908 — west of Albert Edward and
Kivu Lake).
Type : <$ ad., forest 90 kilometres west of Lake Albert Edward, 14. ii. 1908.
Rudolf Grauer leg. No. 2,043.
552. Prinia gracilis yemenensis Hart. = Prinia gracilis yemenensis.
Prinia gracilis yemenensis Hartert, Vog. Pal. Fauna, i. p. 609 (1909 — South Arabia).
Type: <J ad., Sheik Othman (Osman), near Aden, 20. xi. 1898. W. R.
Ogilvie-Grant leg. No. 8.
552 b. Prinia mistacea graueri subsp. nov.
Type : <$ ad., North-western shores of Lake Tanganyika, near Baraka,
14.viii.1908. Rudolf Grauer leg. No. 3,233.
This distinct new form differs from all known ones. From the South African
P. mistacea affinis (Smith) by having a larger and stronger bill, much longer wing
458 NOVITATES ZOOLOGICAE XXVII. 1920.
■
and shorter tail ! The edges of the quills are darker cinnamon, thighs and sides
of abdomen brighter and darker cinnamomeous. Moreover, while the South
African form has a distinct breeding and off-plumage, these do not seem to differ
at all in P. m. graueri. From P. m. tenella of the coastal belt of British East
Africa (terra typica Mombasa), which has a similarly strong bill, in longer wing
and deeper rufous-cinnamon flanks and thighs. From the inland East African
form, which is not the same as tenella, it differs in its stronger bill, generally
shorter tail, and brighter flanks and thighs. Both tenella and the inland East
African form have only one plumage. P. mistacea mistacea (Abyssinia) has finer
bill, darker brown upperside even in the " winter " plumage, less rufous wing-
edges and sides of abdomen. The two plumages are distinct in P. m. mistacea.
Wings of P. m. graueri : J, 54-5-56 ; $, 51-53 mm.
Hob. Near Baraka, north-western shores of Lake Tanganyika, Usumbura,
and Kissenyi on Lake Kivu. Sixteen specimens, all collected by Rudolf Grauer.
553. Suya waterstradti Hart. = Suya waterstradti*
Suya waterstradti Hartert, Nov. Zool. ix. p. 568 (1902 — Gunong Tahan, Eastern Malay Peninsula).
Type : r?, Gunong Tahan, 5—9,000 feet, October 1901. John Waterstradt
leg.
554. Cettia oreophila Sharpe = Horeites {montanus) oreophilus.
Cettia oreophila Sharpe, Ibis, 1888, p. 387 (Kina Balu, Borneo).
Cotype : $ ad., Kina Balu, 8,000 feet, 20. ii. 1888. John Whitehead leg.
No. 2,027.
(I am not sure if this should be considered a subspecies of Horeites montanus,
as Hellmayr does, but the latter view is not without foundation.)
555. Cettia everetti Hart. = Horeites montanus everetti.
Cettia everetti Hartert, Nov. Zool. v. p. 113 (1898 — Atapupu, Timor).
Type : <J ad., Atapupu, Timor, vii.1897. Alfr. Everett leg.
556. Horeites pallidipes osmastoni Hart. = Horeites pallidipes osmastoni.
Horeites pallidipes osmastoni Hartert, Bull. B.O. drub, xxi. p. 107 (June 1908 — Andaman Islands).
Type : <$ ad., Port Blair, ll.xii.1906. R. B. Osmaston leg.
557. Horeites flavolivacea intricatus Hart. = Horeites flavolivaceus intricatus.
Horeites flavolivacea intricatus Hartert, Vog. pal. Fauna, i. p. 533 (1909— Tsin-ling Mts., Shensi,
China).
Type : cJ ad., Sitaipaishan. Tsin-ling Mts., half-way up, 1.x. 1905. Coll. by
Alan Owston's Japanese hunters. No. 11,050.
* Though I follow the Hand-list of Sharpe, on the whole, because a list according to my system
does not exist, I deviated here and in some other cases. PhyUergates is a close ally of Orthotomua
and will be placed near the latter.
Novitates Zoological XXVII. 1920. 459
558. Camaroptera griseoviridis harterti Zedl. = Camaroptera brevicaudata harterti.
Camaroptera griseoviridis harterti Zedlitz, Journ. j. Orn. 1911. p. 342 (Angola).
Type: <J ad., Canhoca, N. Angola, 20. xi. 1903. W. J. Ansorge leg.
No. 1,198.
Zedlitz's Revision of the genus Camaroptera, in Journ. f. Om. 1911, pp. 328-
345, advances our knowledge of this difficult little genus very much and is an
excellent piece of work. Unfortunately, however, it contains a fundamental
nomenclatorial error, because the author, following Reichenow, misunderstood
Cretzschmar's brevicaudata. Neither the figure nor the description can possibly
warrant the assumption that brevicaudata is a form of what is correctly called
superciliaris, with its bright yellowish-green upperside and golden-yellow forehead,
cheeks, and superciliary lines. Zedlitz says that the figures in the Atlas can be
trusted, but it is impossible to stick to them in detail, as a comparison with
actual specimens of other plates will prove. Moreover, Cretzschmar does not
talk of a " schon griine Oberseite," but clearly describes the upperside as oliva-
ceous, merging into pale brown on the head and nape, and with a fine green tinge on
back and wing-coverts ! Evidently the latter has been overdone by the artist,
and the types are the two specimens now in the Senckenbergian Museum, as
carefully described by Zedlitz. Cretzschmar's description is that of the younger
bird, which has some green on the back. To make Zedlitz's and Reichenow's
grouping of the forms acceptable, they had to resort to the somewhat wild theory
that Cretzschmar's brevicaudata is a form of what is rightly called superciliaris,
a group only known from the West African faunal region, the type of which they
assumed to be lost, and which had defied all efforts of future collectors to re-
discover it ! As, however, Riippell's collections were made in Eastern Kordofan,
and Butler and others found there the bird called by Zedlitz G. griseoviridis
griseoviridis, this form must be the true C. brevicaudata brevicaudata.
559. Camaroptera brevicaudata rothschildi Zedl. = Camaroptera superciliaris
rothschildi.
Camaroptera brevicaudata rothschildi Zedlitz, Journ.f. Orn. 1911. p. 331 (Gabun, north to the Gold
Coast).
Type: <J ad., Abanga River, Ogowe River, Gabun, 6.xi.l907. W. J.
Ansorge leg. No. 937.
560. Canmaroptera brevicaudata pulchra Zedl. = Camaroptera superciliaris
pulchra.
Camaroptera brevicaudata pulchra Zedlitz, Journ. f. Orn. 1911. p. 331 (North Angola, east to Lake
Tanganyika).
Type : ? ad., Canhoca, Angola. 15.xi. 1903. W. J. Ansorge leg. No. 1,134
(not 1,143).
It seems to me that pulchra and rothschildi are recognizable subspecies ;
should the two not be separable, rothschildi would be a synonym, as pulchra stands
first on the page. In any case, more material is desired to confirm these forms.
A female named flavigularis by Zedlitz, from the Ogowe River, is, I have no doubt
at all, the young of rothschildi. Could all flavigularis be young birds ? Then
rothschildi would be a synonym of flavigularis 1894 !
460 NOV1TATES ZOOLOGICAE XXVII. 1920.
561. Sylvietta brachyura nilotica Neum. — Sylvietta brachyura nilotica.
Sylvietta brachyura nilotica Neumann, Joxrn. f. Orn. 1906. p. 279 (Akobo, White Nile, Atbara).
Type : $ ad., Shabeisha, White Nile, 23. iv. 1900. Harry F. Witherby leg.
No. 122.
(Cf. Ibis, 1918, p. 670.)
562. Sylvietta ansorgei Hart. = Sylvietta ansorgei.
Sylvietta ansorgei Hartert, Bull. B.O. Club, xix. p. 97 (1907 — Benguella).
Type : <J ad., Huxe, Benguella, 28. vi. 1904. W. J. Ansorge leg. No. 152.
(S. loivei Ogilvie-Grant, 1911, is a synonym. Cf. Ibis, 1918, p. 671.)
562 a. Sylvietta leucophrys chloronota subsp. nov.
Differs from S. leucophrys leucophrys in having the whole back yellowish
green, only the uppermost back being slightly tinged with olivaceous, and the
crown and ear-coverts brighter chestnut. Dimensions the same.
Type : <J ad., primeval forest north-west of Baraka, N.W. of Lake Tan-
ganyika, 1,900 m., 19. xi. 1908. Rudolf Grauer leg. No. 3,852.
Hob. Near Baraka and Kivu region, at elevations of 1,600 to 2,400 m., in
forest.
Compared nine specimens, all collected by Grauer, with six topotypical
ones, collected by Dr. van Someren's hunter and Colonel Meinertzhagen's collector,
Allen Turner.
563. Sylvietta neumanni Rothsch. = Sylvietta neumanni.
Sylvietta neumanni Rothschild, Bull. B.O. Club, xxiii. p. 42 (1908 — West of Lake Tanganyika).
Type : cj ad., primeval forest west of Lake Tanganyika, 2,000 m., 28 . vii . 1908.
Rudolf Grauer leg. No. 3,137.
(?) 564. Apalis flavida malensis Neum. = Apalis (Euprinodes) flavida malensis ?
Apalis flavida malensis Neumann, Orn. Mouatsber. 1905, p. 78 (" Gebiet nordlich des Rudolf-und
Stefanie-Sees ").
Type : <J, " Schambala-Fluss, Male-Land," 21 .i. 1901. Oscar Neumann leg.
No. 631.
Zedlitz (Journ. j. Orn. 1916, p. 90), who has seen 5 males and 2 females,
recognizes this form, but I am doubtful if it should not be united with flavocincta !
Zedlitz's description is not convincing, moreover he compares malensis with
" malensis," but I suppose he meant to say flavocincta.
565. Apalis nigriceps collaris van Som. = Apalis nigriceps collaris.
Apalis nigriceps collaris van Someren, Bull. B.O. Club, xxxv. p. 107 (1915 — Uganda).
Types : (J?, Bugoma Forest, Uganda, 16.x. 1913. Dr. V. G. L. van Someren
leg.
NOVITATES ZoOLOQICAE XXVII. 1920. 461
f 566. Apalis ansorgei Hart. = Eremomela atricollis Boc.
Eremomela atricollis Bocage, Journ. Lisboa (2), xi. p. 153 (1893 — Galanga, Benguella).
Apalis ansorgei Hartert, Bull. B.O. Club, xv. p. 95 (1895 — Bihe, Benguella).
(Of Urolais mariae Alexander we have a paratype, <J, obtained on Mt. St.
Isabel, Fernando Po, 26. xi. 1902. This appears to be one of the only two
specimens collected by the author, whose magnificent collection is now in the
British Museum.)
567. Sericornis meeki R. & H. = Sericornis meeki.
Scricornis meeki Rothschild & Hartert, Nov. Zool. xx. p. 503 (Mt. Goliath, eastern Central Dutch
New Guinea).
Type : " ?," Mt. Goliath, 8 . ii . 1911. A. S. Meek Coll. No. 5,338.
f 568. Sericornis pusilla R. & H. = Sericornis olivacea Salvad.
Sericornis olivacea Salvadori, Ann. Mas. Genova, xxxvi. p. 100 (1896 — Moroka, British New Guinea
Mts.).
Sericornis pusilla Rothschild & Hartert, Nov. Zool. x. p. 228 (1903— Richardson Range, British
New Guinea).
Type : Mt. Gayata, Richardson Range, British New Guinea, 2 — 4,000 feet.
(According to preparation collected by Weiske ?)
569. Sericornis arfakiana Salvad. = Sericornis arfakiana arfakiana.
Sericornis arfakiana Salvadori, Ann. Mus. Civ. Genova, vii. p. 962 (1875 — Arfak Mountains).
Cotype : Mori, Arfak Mts., 3,500 feet, 3. v. 1875. Odvardo Beccari leg.
(ex David). Specimen C of the list of six specimens in Salvadori's Orn. Pap.
ii. p. 408. Marked " Typus ! " by the author.
570. Sericornis arfakiana oorti R. & H. = Sericornis arfakiana oorti.
Sericornis arfakiana oorti Rothschild & Hartert, Nov. Zool. 1913. p. 503 (S.E. New Guinea).
Type : ^ ad., Bihagi, head of Mambare River, 19. ii. 1906. A. S. Meek Coll.
No. A 2,464.
571. Acanthiza nana mathewsi Hart. = Acanthiza nana mathewsi.
Acanthiza nana mathewsi Hartert, Bull. B.O. Club, xxv. p. 82 (1910 — Victoria : Box Hill, Castlemaine,
Mulgrave River, Springvale, Saddleworth. Type Springvale).
Type: <$ ad., Springvale, Victoria, 23.x. 1897. A. C. Campbell leg.
No. 76 a.
572. Acanthopneuste everetti Hart. = Phylloscopus giulianettii everetli.
Acanlhopneuste everetti Hartert, Bull. B.O. Club, viii. p. 31 (1899— Buru) ; cf. Nov. Zool. 1900. p. 239,
1914. p. 389 ; Vog. pal. Fauna, pp. 496, 500.
Type : ad., Mt. Mada (Madang, Gunong Fogka), Buru, 3,000 feet, viii.-ix.
1898. J. Dumas leg.
30
462 Novitates Zoolooicae XXVII. 1920.
573. Cryptolopha everetti waterstradti Hart. = Phylloscopus ghdianettii
waterstradti.
Cryptolopha everetti u'aterstradti Hartert, Nov. Zool. 1903. p. 9 (Batjan and Obi Major).
Type : $, Batjan, vii. 1902, 5-7,000 feet. John Waterstradt leg.
574. Phylloscopus trivirgatus parvirostris Stres. = Phylloscopus trivirgalus
parvirostris.
Phylloscopus trivirgatus parvirostris Stresemann, Nov. Zool. xix. p. 322 (1911 — Mountains of Malay
Peninsula).
Type : (J, Gunong Tahan, Pahang, Eastern Malay Peninsula, 5,200 feet,
13. vii. 1911. Ex Mus. Kwala Lumpur, exchanged.
(This form is very closely allied to P. trivirgatus trivirgatus from Java, Bali,
Lombok, and Sumbawa, but the bill is a little shorter and blackish underneath,
while in P. t. trivirgatus it is chiefly light brown or flesh colour. Four Sumatran
specimens, collected by Robinson and Kloss, belong also to P. t. parvirostris, as
suggested by Stresemann. The wing of the latter is not shorter.)
575. Acanthopneuste floris Hart. = Phylloscopus floris.
Acanthopneuste floris Hartert, Nov. Zool. v. p. 114 (1898 — Flores).
Type : <J, South Flores, 3,500 feet, October 1896. Alfred Everett leg.
576. Phylloscopus trochiloides iokiensis Hart. = Phylloscopus trochiloides
jokiensis
Phylloscopus trochiloides fokiensis Hartert, Bull. B.O. Club, xxxvii. p. 43 (1917 — Fokien, China).
Type : J ad., Kuatun, N.W. Fokien, 15. iv. 1897. J. De La Touche Coll.
577. Acanthopneuste trochiloides harterti Bak. = Phylloscopus trochiloides
harterti.
Acanthopneuste trochiloides harterti Baker, Bull. B.O. Club, xxxi. p. 36 (1913 — Assam Hills, 4,000 —
6,000 feet).
Type : (J, said to have been caught on nest by native, on the peak near
Shillong, 6,000 feet, 13. vi. 1908. E. C. Stuart Baker leg.
In the description, in the eighth line, it should of course be inner webs,
instead of " outer " webs.
578. Phylloscopus goodsoni Hart. = Phylloscopus goodsoni.
Phylloscopus goodsoni Hartert, Nov. Zool. xvii. p. 240 (1910 — Hainan).
Type : $ ad., Lei Mui Mon, Hainan, 12. i. 1903. Katsumata leg.
This might perhaps be a subspecies of P. ricketti ?
NOVITATES ZOOLOGICAE XXVII. 1920. 463
(? f) 579. Phylloscopus sibilatrix erlangeri Hart. = Phylloscopus sibilatrix
erlangeri (or flavescens).
Shylloscopus sibilatrix flavescens Erlanger, Jcmrn. f. Orn. 1899. p. 254. pi. v. (Tunisia).
Phylloscopus sibilatrix erlangeri Hartert, Yog. pal. Fauna, i. p. 516 (1909 — " Scheint die Mittelmeer-
lander zu bewohnen, und zwar Siid-Frankreich, Spanien, Sardinien, Dalmatien bis Serbien,
und vermutlicb Marokko, Tunis und Algier ").
Type : (J ad., Orange Wood in the Mehuila, on the Durn-er-Rebia, east of
Mazagan, West Marocco, 8.iv.l901. Ernst Hartert leg.
It is doubtful if this name is valid. I named these paler, more yellowish
birds erlangeri, because there was already a Sylvia flavescens and Phyllopneuste
flavescens of Gray, but there is no Phylloscopus flavescens. I am afraid, therefore,
that I wrongly interpreted the Rules of Nomenclature, and that the name
flavescens may be used. Moreover, I do not any longer believe that any sibilatrix
breeds in Africa, but consider flavescens (or erlangeri) a South European form,
merely differing very slightly by being more yellowish from P. sibilatrix sibilatrix.
Cf. NOVITATES ZOOLOGICAE, XX. p. 49 (1913).
580. Phylloscopus borealis examinandus Stres. = Phylloscopus borealis
examinandus.
Phylloscopus borealis examinandus Stresemann, Nov. Zool. xx. p. 353 (1913 — Bali, Sumbawa, Flores,
Alor, and Sumba, in winter !).
Type : <J ad., Bali, iii. 1896. William Doherty leg.
This apparent subspecies is so far only known in winter quarters, on the
Lesser Sunda Islands to Alor, east of Bali. Observations in the breeding places
will have to confirm this form before it can be said to be finally established, but
it seems to be different.
581. Phylloscopus collybita exsul Hart. = Phylloscopus collybita exsul.
Phylloscopus collybita exsul Hartert, Vog. pal. Fauna, i. p. 505 (1907 — Lanzarote).
Type : $ ad., Lanzarote, 22.xii.1903. Polatzek leg. No. 2,223.
582. Sylvia deserticola maroccana Hart. = Sylvia deserticola maroccana.
Sylvia deserticola maroccana Hartert, Bull. B.O. Club, xxxviii. p. 6 (1917 — Western Atlas, in Marocco).
Type : ^ ad., Sek.sa.wa, Western Atlas, Marocco, 27. iii. 1906. F. W. Riggen-
bach leg. No. 1,730.
This is one of the most interesting discoveries of Mr. Riggenbach in Marocco.
The " typical " S. deserticola deserticola, as we now well know, nests in the southern
or Saharan Atlas Ranges and mountains of the Haux Plateaux (near Batna,
Djelfa, etc.), in Algeria and Tunisia. Of S. d. maroccana Riggenbach only sent
one male, but its differences are beautifully confirmed by a specimen collected
by Mr. Meade- Waldo near Tsauritz Entsagauz, where it was common.
583. Sylvia undata toni Hart. = Sylvia undata toni.
Sylvia undata toni Hartert, Vog. pal. Fauna, i. p. 602.
Type : ^ ad., south of Biskra, S. Algeria, 14. i. 1903. Ernst Fliickiger leg.
No. 327.
464 Novitates Zoolooicae XXVII. 1920.
584. Tatare familiaris Rothsch. = Acrocephalus familiaris.
Tatare familiaris Rothschild, Ann. & Mag. Nat. Hist. (6), x. p. 109 (1892 — Laysan Island).
Type : <J ad., Laysan Island, 18. vi. 1891. H. C. Palmer leg. No. 1,092.
585. Acrocephalus arundinaceus zarudnyi Hart. = Acrocephalus arundinaceus
zarudnyi.
Acrocephalus arundinaceus zarudnyi Hartert, Bull. B.O. Club, xxi. p. 26 (1907 — Turkestan, terra
typica Djarkent) ; Vog. pal. Fauna, p. 558.
Type: c?ad., Djarkent, Turkestan, 21. iv. 1900 (Russian date). N. Zarudny
leg. No. 1,566.
(?) 586. Calamoherpe griseldis Hartl. = Acrocephalus arundinaceus griseldis.
Calamoherpe griseldis Hartlaub, Abh. Nat. Ver. Bremen, xii. p. 7 (1891 — Nguru).
Type : Nguru, Emin Pasha leg. Received from Hartlaub.
Sharpe (Hand-list, iv. p. 206) places this bird in the genus Calamocichla, but
it is nothing than a very small Acrocephalus arundinaceus ! It might be a
dwarf of the latter. The wing measures only 85 mm. Or it might be a small
subspecies of the Great Reed-Warbler, either breeding in tropical Africa or
wintering there as a visitor from somewhere in the palaearctic fauna.
587. Calamocichla cunenensis Hart. = Calamocichla cunenensis.
Calamocichla cunenensis Hartert, Bull. B.O. Club, xiii. p. 62 (1903 — Cunene River, S.W. Africa).
Type : Cunene River (probably south of), 3.iv.l880. A. W. Ariksson leg.
The species of Calamocichla are Reed-Warblers closely allied to Acrocephalus,
but with a more rounded wing, the first primary being much longer, the second
shorter, and resident, non-migratory, in Tropical Africa. Neumann gave an
excellent review of the genus in Novitates Zoologicae, 1908, pp. 244—252. In
the Hand-list Sharpe has at last placed Calamocichla and Acrocephalus in the
same family, while in the Cat. B. they were in different volumes !
588. Calamocichla zuluensis Neum. = Calamocichla leptorhyncha zuluensis.
Calamocichla zuluensis Neumann, Bull. B.O. Club, xxi. (not xx. !) p. 96 (1908 — Zululand and South
Mozambique) ; Nov. Zool. 1908. p. 248.
Type : Ad. Eschowe, Zululand. Woodward Bros. leg.
This form requires further confirmation and can only be a subspecies of
leptorhyncha. Neumann was certainly wrong in uniting the Upper Shire
specimen with leptorhyncha, as it agrees perfectly with the type of zuluensis.
C. gracilirostris is a much larger bird.
589. Calamocichla ansorgei Hart. = Calamocichla ansorgei ansorgei.
Calamocichla ansorgei Hartert, Bull. B.O. Club, xvi. p. 52 (1906 — Duque de Braganza, N. Angola).
Type : (J ad., Duque de Braganza, 2. viii. 1903. W. J. Ansorge leg. No. 850.
Novttates Zoolooioae XXVII. 1920. 465
590. Calamonastes fasciolatus pallidior Hart. = Calamonastes fasciolatus
pallidior.
Calamonastes fasciolatus pallidior Hartert, Bull. B.O. Club, xix. p. 97 (1907 — Huxe, " Sandpits," and
Makonjo in Benguella).
Type: <J ad., "Sandpits," Benguella, 8.vii.l904. W. J. Ansorge leg.
No. 259.
t 591. Cisticola floweri Hart. = Cisticola ruficeps.
Cisticola floweri Hartert, Bull. B.O. Club, xxvii. p. 12 (Sennaar, Blue Nile) ; fig. Ibis, 1918. pi. x.
fig. 8.
Type : Sennaar, Blue Nile, 28. vii. 1909. S. S. Flower leg. No. 870.
Messrs. Sclater and Mackworth-Praed, Ibis, 1918, p. 651, say that the series
in the British Museum prove that C. ruficeps has a very distinct seasonal change
of plumage, the winter birds having the back boldly striped with black and
yellowish, while the summer birds (described by me as O. floweri) have the back
plain greyish brown, with very faint traces, of darker stripes to the centres of
the feathers. Though it has been known for some time that the winter and
summer plumages of many Cisticolae differ (for example, the head being either
uniform rufous or boldly streaked in C. exilis), this was not known in the case
of C. ruficeps.
Messrs. Sclater and Mackworth-Praed separate the Kordofan form Cisticola
ruficeps ruficeps and the Upper Nile and Sennaar one as E. ruficeps scotoptera.
This, however, requires confirmation, for on two specimens collected by A. L.
Butler at Gedaref (east of Sennaar), in April 1901 (boldly streaked but much
worn, evidently shortly before the moult), Oscar Neumann made a note on the
labels saying that he compared them with the types of ruficeps in the Frankfurt
and Berlin Museums from Kordofan and found them completely alike in plumage.
(?) 592. Cisticola neumanni Hart. = Cisticola prinioides neitmanni (or
Cisticola prinioides prinioides ?).
Cisticola neumanni Hartert, Bull. B.O. Club, xii. p. 13 (1901— Mt. Kenya).
Type : Western slope of Mt. Kenya, 10,000 feet, 7.viii. 1899. J. Mackinder
leg. No. 46.
This form requires confirmation by a series. Are not C. prinioides and
C. hunteri perhaps seasonal forms of the same species ?
593. Cisticola cisticola arabica Hart. = Cisticola cisticola arabica.
Cisticola cisticola arabica Hartert, Nov. Zool. 1917. p. 458 (South Arabia — Yemen and Lahej).
Type : Hajeilah, Yemen, 2,080 feet, l.iv. 1913. G. W. Bury leg. No. 583.
594. Cisticola natalensis inexpectata Neum. = Cisticola natalensis inexpectata.
Cisticola natalensis inexpectata Neumann, Journ. f. Orn. 1906. p. 268 (Shoa and Lake Abassi).
Type : $, Lake Abassi, 5. xii. 1900 (not 4. xii. 1900). Oscar Neumann leg.
No. 352.
466 • Novitates Zoolooicae XXVII. 1920.
595. Cisticola erythrogenys djamdjamensis Neum. = Cisticola lugubris
djamdjamensis.
Cisticola erythrogenys djamdjamensis Neumann, Journ.f. Orn. 1904. p. 163 (Djamdjam) ; id., op. cit.
1906. p. 269.
Type : $, Abera in Djamdjam, 16.xii. 1900. Oscar Neumann leg. No. 429.
After studying these Cisticolae with Dr. van Someren I have come to the
conclusion that erythrogemjs is the non-breeding plumage of lugubris ! Therefore
erythrogenys becomes a synonym of lugubris and djamdjamensis a subspecies
of lugubris.
596. Cisticola robusta schraderi Neum. = Cisticola robusta schraderi.
Cisticola robusta schraderi Neumann, Journ.f. Orn. 1906. p. 265 (" Nord-Abyssinien").
Type: Senate, N. Abyssinia, 7,500 feet, 10. i. 1903 (not 1902!). Gustav
Schrader leg.
f 597. Cisticola blanfordi sobatensis Neum. = Cisticola lugubris marginata.
Cisticola blanfordi sobatensis Neumann, Orn. Monatsber. 1904. p. 164 (Sobat).
Type : $, Diek, on the Akobo River, one of the source rivers of the Sobat,
28. v. 1901. Oscar Neumann leg. No. 1,255.
Neumann (Journ. f. Orn. 1906, p. 270) declares, after comparing the type of
blanfordi, that his sobatensis is the same as blanfordi. Sclater and Mackworth-Praed
(Ibis. 1918, p. 647) adopt the name marginata Heugl. for this form, treating it,
as Neumann did in 1906, as a subspecies of C. lugitbris. I am convinced that
Neumann as well as Sclater and Praed were right in their conclusions, and that
therefore C. b. sobatensis is a synonym of C. I. marginata, described by Heuglin,
Ibis, 1869, p. 94, pi. i. fig. 1, from the White Nile between Fashoda and Lado.
This form is closely allied to haematocephala, and it would be a great help
if the differences, in the various plumages, between marginata and haematocephala
(1868) were clearly described.
598. Cisticola ansorgei Neum. = Cisticola subruficapilla ansorgei.
Cisticola ansorgei Neumann, Bull. B.O. Club, xvi. p. 114 (1906 — " Benguella").
Type: <J ad., Caconda, Benguella, 7.ix.l904 (not " 2.ix. 1904 "). W. J.
Ansorge leg. No. 893.
598 a. Cisticola tinniens perpulla subsp. nov.
Type: <J ad., Bailundu country, Benguella, 18. viii. 1901. C. Hubert
Pemberton leg.
Differs from C. tinniens tinniens in being darker. The crown is of a less
bright, darker brown, and the blackish streaks are, as a rule, less obvious ; the
edges to the feathers of the back are narrower, darker, and more brownish, so
that the whole upperside looks much darker ; the margins of the tail-feathers
are of a less bright and darker brown, the tips of the lateral pairs have less
sharply defined black anteapical cross-bars. Underside of a duller, more greyish,
less buffy-yellowish coloration. Wings : 2 ^, 60 and 61-5 ; 2 ?, 54 and 55 mm.
Novitates Zoological XXVII. 1920. 467
" Iris neutral orange. Feet light brown, brown-ochre, brown flesh-colour.
Bill black, lower pale " (Ansorge).
Hob. Benguella : Quando River, 20.xii.1904 (W. J. Ansorge); Cuan-
hangamma River, 17. ix. 1904 (W. J. Ansorge) ; Bulu-Bulu, in Bihe, 4.x. 1904;
Bailundu, 18. viii. 1901. C. H. Pemberton. All these localities are inland (east)
of the town of Benguella.
f 599. Cisticola simplicissima Neum. = Cisticola anguslicauda Rchw.
Cisticola angusticauda Reichenow, Journ.f. Orn. 1891. pp. 69, 163 (Gonda, Tabora).
Cisticola simplicissima Neumann, Bull. B.O. Club, xxiii. p. 47 (1908 — " Benguella").
Type : <J, Kukema River, Bihe, Benguella, 8.xii. 1904. W. J. Ansorge leg.
No. 870.
The type is not fully adult. There can be no doubt that it is the same species
as angusticauda, which extends westwards to Benguella. I do not understand
why Neumann did not allude to angusticauda, while comparing his supposed new'
species with C. rufa. C. muelleri Alex. (1899) appears to be also angusticauda !
t 600. Cisticola hypoxantha Hartl. = Cisticola rufa (? a subsp.).
Drymoica rufa Fraser, Proc. Zool. Soc. London, 1843. p. 17 (" River Quorra, opposite Iddah ").
Cisticola hypoxantha Hartlaub, Proc. Zool. Soc. London, 1880. p. 624 (" Magungo, December 11 "
Errore: The specimen is labelled "Magungo, 19.11.1879," and the eleventh month is
November).
Type: (J juv., Magungo, 19. xi. 1879. Emin Pasha leg. No. 122.
There is no doubt that Hartlaub's hyyoxantha is the young bird of C. rufa,
which has, like so many Cisticolae, a yellow underside. It is, however, possible
that C. rufa can be subdivided into several subspecies, but even if the East
African form is separated I believe " hypoxantha " would remain a synonym
of rufa.
t 601. Phyllergates * cinereicollis Sharpe = Phyllergates cucullatus cucullatus.
Orthotomus cucullatus Temminck, PI. Col. 599. fig. 2 (1836 — Java, Sumatra).
Phyllergates cinereicollis Sharpe, Ibis, 1888, p. 479 (Kina Balu, N.E. Borneo).
Type: <$ ad., Kina Balu, 4,000 feet, 10. ii. 1888. John Whitehead leg.
No. 2,101.
In Novitates Zoologicae, iv. pp. 517, 518, I said that most likely
cinereicollis would not be separable from cucullatus. This is indeed the case —
Bornean and Javan, as well as Sumatran specimens (sumatranus Salvad.), are
absolutely inseparable, and so are those from the Malay Peninsula. Stresemann
(Novitates Zoologicae, xix. 1912, pp. 341, 342) has also come to this conclusion.
Stresemann also points out that my statement, that the outer rectrices in Javan,
Malaccan, and Bornean specimens had no white at all, was not quite correct ;
this is true, at the same time a (more or less narrow) white outer edge to the
lateral rectrices is very rare and only seen in our series in a few skins from the
Malay Peninsula, and one from Java, so that the absence or diminished extent
* Though, for the sake of convenience, I follow Sharpe's Hand-list in this List, in reversed order,
I cannot do so in all cases. In this case, for example, I have to deviate : Phyllergates is closely
allied to Orthotomus, while Sharpe placed 56 genera between them.
468 NoVITATES ZOOLOQICAE XXVII. 1920.
of white markings in P. cucullatus cucullatus is still a very good character to
distinguish it from P. cucullatus coronatus from India and Burma. Stresemann
also unites P. c. philippinus with cucullatus cucullatus, but I do not agree to this.
It is true that the character by which I distinguished philippinus, i.e. a narrow
white mark on the two outer rectrices, is not constant, but the crown and back
of Philippine specimens are slightly lighter, so that I shall, for the present,
keep philippinus separate. (Of P. heterolaemus Mearns from Mindanao I have
not been able to examine specimens. It seems to be quite different. )
602. Phyllergates cucullatus philippinus Hart. = Phyllergates cucullatus
philippinus.
Phyllergates cucullatus philippinus Hartert, Nov. Zool. iv. p. 517 (1897 — North Luzon).
Type: <$ ad., Benguet, North Luzon, 2 . iii . 1894. John Whitehead leg.
'No. 276.
See remarks under 601. More material desired !
603. Phyllergates everetti Hart. = Phyllergates cucullatus everetti.
Phyllergates everetti Hartert, Nov. Zool. iv. p. 517 (1897— S. Flores).
Type : cJ ad., South Flores, above 3,500 feet, November 1896. Alfred
Everett leg.
604. Phyllergates everetti dumasi Hart. = Phyllergates cucullatus dumasi.
Phyllergates everetti dumasi Hartert, Bull. B.O. Club, viii. p. 31 (1899— Mt. Mada, Buru) ; Nov. Zool.
1900. p. 238. 1914. p. 390.
Type : ^ ad., Mt. Mada (Madang), 3,000 feet, September 1898. J. Dumas
leg.
605. Phyllergates cucullatus batjanensis Hart. = Phyllergates cucullatus
batjanensis.
Phyllergates cucullatus batjanensis Hartert, Bull. B.O. Club, xxxi. p. 2 (1912 — " Batjan, Northern
Moluccas ").
Type : J ad., Batjan, 5,000 — 7,000 feet, July 1902. J. Waterstradt leg.
606. Orthotomus chloronotus Grant = Orthotomus chloronotus.
Orthotomus chloronotus Grant, Bull. B.O. Club, v. p. ii. (1895 — " Cap Engano, N.E. Luzon ") ; Ibis,
1896. p. 117. pi. iii. fig. I.
Type and single specimen : cJ ad., Cap Engano, N.E. Luzon, 22. iv. 1895.
John Whitehead leg. No. A 279.
607. Bradypterus alfredi Hartl. = Bradypterus alfredi alfredi.
Bradypterus alfredi Hartlaub, Journ.f. Orn. 1890. p. 152 (" Njangalo," err. : should be Njangabo).
Type : ? ad., Njangabo, 3. v. 1889. Emin Pasha leg. No. 212.
NOTITATES ZOOLOGICAE XXVII. 1920. 469
(?) 608. Bradypterus cinnamomeus pallidior Neum. = Brady pterus cinnamomeus
pallidior.
Bradypterus cinnamomeus -pallidior Neumann, Orn. Monatsber. 1914. p. 10 (" Gebirge westlich dea
Tanganyka ").
Type : <j>ad. (not" J "), primeval forest west of Baraka, 1,900 m., l.xii.1908.
, Rud. Grauer leg. No. 3,819.
This form requires confirmation. The type is very pale, but in the same
region we find quite dark birds like cinnamomeus.
609. Stasiasticus montis Hart. = Bradypterus montis.
Stasiasticus montis Hartert, Nov. Zool. iii. p. 540 (1896 — Mt. Arjuno, Eastern Java).
Type : <J, Mt. Arjuno, 9—10,000 feet, January 1896. William Doherty leg.
It is, in my opinion, absolutely certain that my genus " Stasiasticus" was
founded on wrong premises. I compared it with Androphilus and Pseudo-
tharraleus, but it is really congeneric with the birds generally called Lusciniola —
i.e. thoracica, luteiventris, seebohmi, etc. These latter are, however, inseparable
from the African Bradypterus, in every way. They must, therefore, all be called
Bradypterus. The only further question is, whether they can really be united
with Lusciniola (type melanopogon), as I did in Vog. pal. Fauna, p. 540, or whether
they should be separated as has been done by Oates and Sharpe. I think it will
be better to separate them, because Lusciniola melanopogon has the tail less
graduated, the wings comparatively longer, the plumage not quite so copious.
We would then have :
Lusciniola with melanopogon and subsp. alone, Bradypterus with brachypterus
(genotype), and about 14 other African forms, and pryeri, taczanowskia, luteo-
ventris, major, thoracica, seebohmi, montis, russula.
610. Lusciniola seebohmi Grant = Bradypterus seebohmi.
Lusciniola seebohmi Grant, Bull. B.O. Club, iv. p. xl. (1895 — North Luzon).
Type : $, Province of Lepanto, North Luzon, 28.xii. 1894. John Whitehead
leg. No. 931.
611. Bradypterus brachypterus centralis Neum. = Bradypterus brachypterus
centralis.
Bradypterus brachypterus centralis Neumann, Bull. B.O. Club, xxi. p. 55 (1908 — "East and East
Central Africa, from Kikuyu to Lake Kivu ").
Type : $, River bank between Mkingo and Mubera (on the route from
Kagera to Kiva), 6.viii.l907. Rud. Grauer leg. No. 950.
More information about this form is greatly desired. Besides the type there
is in the Tring Museum a <J collected by William Doherty at the Escarpment,
Kikuyu Mountains, October 1900, which probably belongs to centralis, with the
type locality Kivu region !
612. Bradypterus graueri Neum. = Bradypterus graueri.
Bradypterus graueri Neumann, Bull. B.O. Club, xxi. p. 56 (1908 — " Western Kivu Volcanoes ").
Type and unique specimen : £, edge of swamp, Western Kivu Volcanoes,
2,200 m., 17.viii.1907. Rud. Grauer leg. No. 991.
470 Novitates Zoolooicae XXVII. 1920.
This form badly requires confirmation ! It is in good fresh plumage, while
the type of centralis is in very much worn garb. This is peculiar, as both were
shot in August ; the latter may be juvenile, but it does not look so ! Another
question is; if both could not be the same bird ? B. graueri, however, is much
larger, and we do not know that the sexes differ appreciably in size in the genus.
613. Bessonornis (? Cossypha) gambagae Hart. = Oenanthe familiaris
gambagae.
Bessonornis (Cossypha) gambagae Hartert, Bull. B.O. Club, x. p. v. (1899 — Gambaga, Gold Coast
Hinterland).
Type : " ?," Gambaga, 27.viii. 1898. Capt. W. Giffard leg.
I must confess that I am still somewhat in doubt about the genus in which
this bird should be placed. I admit that I, following Sharpe's arrangement in
the British Museum, was wrong in placing this form in " Bessonornis,'" which is,
apparently, not separable from Cossypha. Reichenow certainly came near the
truth when he placed jamiliaris, galtoni, and jalkensteini in Phoenicurus. I
would gladly agree to this, if I did not consider that they are still better placed
in Oenanthe. Will anyone point out a generic difference between Oenanthe
chrysopygia and the disputed jamiliaris, galtoni, jalkensteini, gambagae, omoensis ?
This, of course, raises the question of what the differences are between Oenanthe
(formerly Saxicola) and Phoenicurus ? That they are very unsatisfactory may be
gathered from comparing the generic characters described in vol. v. of the Cat.
B. Brit. Mus., Reichenow's Vog. Ajr. iii. (where they are most wrongly placed
in two different subfamilies !), and my Vog. pal. Fauna, i. I still believe, however,
that they can be kept separate, though they are closely allied, by the following
characters :
In Oenanthe the bill is comparatively larger, tail comparatively shorter.
In Phoenicurus the beak is weaker, tail comparatively longer. The artificial
distinction of the proportion of the tail and bill used by Seebohm holds good,
though it is not a nice one. If the above distinction is accepted, the familiaris
group goes into Oenanthe by its bill, while the tail is not really shorter, except
by comparison with the bill ! I am certainly of opinion that galtoni, jalkensteini.
gambagae, and omoensis are subspecies, and that gambagae is not identical with
jalkensteini, having the under tail-coverts reddish.
614. Saxicola galtoni omoensis Neum. = Oenanthe jamiliaris omoensis.
Saxicola galtoni omoensis Neumann, Orn. Monalsher. 1904. p. 163 (" Omo-Gebiet ").
Type : ^ ad., Baka in Konta, 28. ii. 1901. Oscar Neumann leg. No. 949.
It must be said that the two specimens collected by Neumann are in very
badly worn plumage, evidently shortly after the breeding season, and that a
series of fresh specimens are desirable to better explain the differences of this
undoubtedly recognizable form.
615. Oenanthe leucopyga aegra Hart. = Oenanthe leucopyga aegra.
Oenanthe leucopyga aegra Hartert, A'tw. Zool. xx. p. 55 (1913 — Algerian Sahara).
Type: <$ ad., Jara Krima, near Ouargla, 10. iii. 1914. E. Hartert and
C. Hilgert leg. No. 206.
NoVITATES ZOOLOGICAE XXVII. 1920. 471
616. Saxicola leucurus riggenbachi Hart. = Oenanthe leticurus riggenbachi.
Saxicola leucurus riggenbachi Hartert, Falco, 1909. p. 36 (Rio de Oro).
Type : (J ad., Rio de Oro, west coast of Sahara, nearly under the tropic of
the cancer, 4.vii.l902. F. W. Riggenbach leg. No. 21.
617. Saxicola seebohmi Dixon = Oenanthe oenanthe seebohmi.
•Saxicola seehohmi Dixon, Ibis, 1882. p. 563. pi. xiv. (Djebel Mahmel, S.E. Algeria).
Type : (£ ad.), Djebel Mahmel (on the label " Djebel Aures, 5,500 feet "),
2. v. 1882. H. J. Elwes and C. Dixon leg. Labelled "Type," apparently by
Dixon. (Ex coll. H. J. Elwes.)
The collectors only shot two males, not knowing that they had found a new
form. Cotype (a paratype) in the British Museum.
618. Cercomela melanura erlangeri Zedl. = Cercomela melanura erlangeri.
Cercomela melanura erlangeri Zedlitz, Journ.f. Orn. 1912. pp. 497, 556 (South Arabia).
Type : <J, Khareba, South Arabia, 12.x. G. W. Bury leg. No. 404.
619. Oreicola ferrea haringtoni Hart. = Oreicola ferrea haringtoni.
Oreicola ferrea haringtoni Hartert, Vog. pal. Fauna, i. p. 7lT (1910 — " Mupin und andere Teile von
Szetschwan bis Fokien und Siidost-China, ausserdem Birmah und die Berglander siidlich des
Brahmaputra."
Type: cJ ad., Lieng-kiang, near Foochow, China, 18. i. 1887. No. 1,445.
620. Pinarochroa sordida schoana Neum. = Pinarochroa sordida schoana.
Pinarochroa sordida schoana Neumann, Journ.f. Orn. 1906. p. 290 (" Gebirge des eigentlichen Schoa
gwischen dem Abai, oberen Blauen Nil, und dem Hauasch ").
Type: <J, Abuje, Schoa, 29. ix. 1900. Oscar Neumann leg. No. 110.
621. Pinarochroa sordida djamdjamensis Neum. = Pinarochroa sordida
djamdjamensis.
Pinarochroa sordida djamdjamensis Neumann, Journ.f. Orn. 1906. p. 291 (Abera, in Djamdjam).
Type : (J, Abera, inDjamdjam, 19.xii. 1900. Oscar Neumann leg. No. 443.
622. Pratincola caprata albonotata Stres. = Saxicola caprata albonotata.
Pralincola caprata albonotata Stresemann, Nov. Zool. xix. p. 321 (1912— Celebes, Buton, Saleyer).
Type : $, Indrulaman, S. Celebes, 3.x. 1895. Alfred Everett leg.
623. Pratincola caprata rossorum Hart. = Saxicola caprata rossorum.
Pralincola caprata rossorum Hartert, Journ.f. Orn. 1910. p. 180 ("Transkaspien, Teile von Persien,
Afghanistan, Peschawar, Kohat und Kaschmir, iiberwintert in den Ebenen des nordwest-
lichen Indiens ").
Type: $, Merw, Transkaspia, 22.vii.1889, Russ. date (= 4.viii. 1889).
N. Zarudny leg. No. 338.
472 NOVITATES ZOOLOQICAE XXVII. 1920.
624. Pratincola torquata hibernans Hart. = Saxicola torquata hibernans.
Praiincola torquata hibernans Hartert, Journ. f. Orn. 1910. p. 173 (Great Britain and Ireland).
Type : $ ad., Tring, 14. xi. 1898. Ernst Hartert leg.
f 625. Pratincola emmae Hartl. = Saxicola torquata axillaris.
Pratincola axillaris Shelley, Proc. Zool. Soc. London, 1884. p. 556.
Pratincola emmae Hartlaub, Journ. f. Orn. 1890. p. 152 (Ruganda).
Type : <J ad., Ruganda (Nkole), 15.vii. 1889. Emin Pasha leg. No. 263.
f 626. Pentholaea baucis Hartl. = Pentkolaea clericalis.
Peniholaea clericalis Hartlaub, Orn. Centralbl. 1882. p. 91.
Pentholaea baucis n. sp. ? Hartlaub, Zool. Jahrb. ii. p. 318 (1884 — Babira, Rimo).
Type: "J," Babira, Upper White Nile, 16. xi. 1882. Emin Pasha leg.
No. 301. (Evidently a bird of the year.)
627. Pentholaea albifrons pachyrhyncha Neum. = Pentholaea albifrons
pachyrhyncha.
Pentholaea albifrons pachyrhyncha Neumann, Journ.f. Orn. 1906. p. 289 (" Omo-Gebiet ").
Type : <^ad., " Uba, Westabhang," Omo region, 27. i. 1901. Oscar Neumann
leg. No. 678.
Neumann also mentions a second specimen which was originally sexed " <J."
In his article, I.e., he doubts this and says that he believes it to be a female. The
dull remiges seem to me clearly to indicate that it is a bird of the year 1900, and
on the forehead white feathers are clearly replacing the black ones. Therefore,
the bird appears to be a male changing into the adult plumage. Females of the
allied species and of P. albifrons albifrons have, as a rule, no white on the forehead.
628. Erythropygia hartlaubi Rchw. = Erythropygia hartlaubi.
Erythropygia hartlaubi Reichenow, Journ. f. Orn. 1891. p. 63 (" Mutjara ") ; Hartlaub, Abh. naturw
V'er. Bremen, xii. 1. p. 9. 1891 (Mutjora).
Type: ^ ad., Mutjora, 13. vi. 1889. Emin Pasha leg. No. 253.
629. Erythropygia paena damarensis Hart. = Erythropygia poena damariensis.
Erythropygia paena damarensis Hartert, Bull. B.O. Club, xix. p. 96 (1907 — Damaraland).
Type : Omaruru, Damaraland, 4. xii. 1879. A. W. Eriksson leg.
630. Erythropygia paena benguellensis Hart. = Erythropygia paena benguellensis.
Erythropygia paena benguellensis Hartert, Bull. B.O. Club, xix. p. 96 (1907— Benguella).
Type : ^ ad., Huxe, Benguella, 21. vi. 1904. W. J. Ansorge leg. No. 83.
631. Erythropygia reichenowi Hart. = Erythropygia reichenowi.
Erythropygia reichenowi Hartert, Bull. B.O. Club, xix. p. 95 (1907 — Angola).
Type : <J ad., Canhoca, Angola, 27. xi. 1903. W. J. Ansorge leg. No. 1,291.
This species is nearly allied to E. quadrivirgata (wrongly placed in Cossypha
by Sharpe) from East Africa.
NOVITATES ZOOLOGICAE XXVII. 1920. 473
632. Neocossyphus rufus gabunensis Neum. = Neocossyphus rufus gabunensis.
Neocossyphus rufus gabunensis Neumann, Bull. B.O. Club, xxi. p. 77 (1908 — ■" South Cameroon to
the Ogowe River ").
Type: $ ad., Ohumbe, Lake Onange, Ogove River, Gabun, 18.vii.1907.
W. J. Ansorge leg. No. 528.
633. Cossypha giffardi Hart. = Cossypha albicapilla giffardi.
Cossypha giffardi Hartert, Bull. B.O. Club, x. p. 5 (1899 — Gambaga).
Type : cJ ad., Gambaga, 29.viii. 1898. Capt. W. Giffard leg.
634. Cossypha somereni Hart. = Cossypha polioptera somereni.
Cossypha somereni Hartert, Bull. B.O. Club, xxxi. p. 3 (1912 — Kyetume).
Type: Kyetume, near Kampala, Uganda, 14. xii. 1911. Dr. V. G. L. van
Someren leg. No. 11.
635. Cossypha semirufa saturatior Neum.= Cossypha semiruja saturatior.
Cossypha semirufa saturatior Neumann, Orn. Monatsber. 1906. p. 7 (" Gebiet der siidathiopischen
Seen und Omo-Gebiet ").
Type: $ ad., Bola Goschana, in Doko, 12. ii. 1901. Oscar Neumann leg.
No. 786.
636. Cossypha roberti rufescentior Hart. = Cossypha roberti rufescentior.
Cossypha roberti rufescentior Hartert, Bull. B.O. Club, xxiii. p. 9 (1908 — West of Lake Albert Edward).
Type : 3 ad., Forest, 90 kilometres west of Lake Albert Edward, 1,600 m.,
12.ii. 1908. Rudolf Grauer leg. No. 2,019.
637a. Kittacincla macrurus omissa Hart. = Kittacincla macrurus omissa.
Kittacincla macrurus omissa Hartert, Nov. Zool. ix. p. 572 (1902 — Java).
Type: $ ad., Lawang, East Java, l.xi.1886. John Whitehead leg.
No. 893.
(Of Cittocincla nigrorum Grant, a synonym of C. superciliaris (Ibis, 1896,
p. 547), we have the " type of the female," but not that of the male.)
638. Xenocopsychus ansorgei Hart. = Xenocopsychus ansorgei.
Xenocopsychus ansorgei Hartert, Bull. B.O. Club, xix. p. 87 (Lobango, Mossamedes).
Type : (J ad., Lobango, Mossamedes, Angola, 18.ii. 1906. Dr. W. J. Ansorge
leg. No. 287.
639. Tarsiger indica formosanus Hart. = Tarsiger indicus formosanus.
Tarsiger indica formosanus Hartert, Bull. B.O. Club, xxv. p. 32 (1909 — Formosa).
Type : <$ ad., Mt. Arizan, Formosa, 4. xii. 1906. Collected by Alan Owston's
Japanese collectors.
474 NOVITATE8 Zoolooicae XXVIL 1920.
640. Larvivora ruflceps Hart. = Luscinia (Larvivora) ruficeps.
Larvivora ruficeps Hartert, Bull. B.O. Club, xix. p. 50 (1907— Tain-ling Mts.) ; Ibis, 1907. pi. xiii.
Type: J ad., Ta-pai-shan, Tsin-ling Mts., 13.vii.1905. Collected by Alan
Owston's Japanese collectors.
641. Larvivora wickhami Baker = Luscinia (Larvivora) wickhami.
Larvivora wickhami Baker, Nov. Zool. xxiii. p. 298 (1916 — Chin Hills).
Type : Adult, Chin Hills, 5,000 feet, April 1916. P. Wickham leg.
642. Luscinia pectoralis confusa Hart. = Luscinia (Calliope) pectoralis confusa.
Luscinia pectoralis confusa Hartert, Vog. pal. Fauna, i. p. 740 (1910 — " Ini ostlichen Himalaya ").
Type : <J ad., Sikkim, i. 1876. H. J. Elwes leg.
643. Erithacus rubecula melophilus Hart. = Erithacus rubecula melophilus.
Erithacus ruljecula melophilus Hartert, Nov. Zool. 1901. p. 317 (Aus den Wander], e. Naturf. p. 98)
(" Meines Wissens nur die britischen Inseln ").
Type : Barnet, near London, 14.xii.1896. W. Burton leg.
644. Erithacus rubecula witherbyi Hart. = Erithacus rubecula witherbyi.
Erithacus rubecula witherbyi Hartert, Vog. pal. Fauna, i. p. 753 (1910 — " Brut-und augenscheinlich
Standvogel im nordlichen Atlas").
Type: <J ad., Hammam R'hira, Northern Algeria, 27. iv. 1904. Harry F.
Witherby leg. No. 100.
645. Phoenicurus frontalis sinae Hart. = Phoenicurus frontalis sinae.
Phoenicurus frontalis sinae Hartert, Bull. B.O. Club, xxxviii. p. 78 (1918 — " Mountains of China :
Mupin and Setchuan to Kansu and Ala-schan mountains, and to the Tsinling range ").
Type : (J ad., Kansu, March 1884, Przewalski leg.
646. Microcichla scouleri fortis Hart. = Microcichla scouleri fortis.
Microcichla scouleri fortis Hartert, Vog. pal. Fauna, i. p. 761 (1910 — Formosa).
Type : c? ad., Tapposha, Formosa, 19.i. 1907. Collected by Alan Owston's
Japanese collectors.
647. Henicurus borneensis Sharpe = Enicurus leschenaulti borneensis.
Henicurus borneensis Sharpe, Ibis, 1889. p. 277 (Kina Balu, Northern Borneo).
Types (marked as such by the author) : <J $ ad., Kina Balu, 3,000 feet,
29 . iii . and 13. iv. 1888. John Whitehead leg. Nos. 2,338 and 2,433.
648. Enicurus leschenaulti indicus Hart. = Enicurus leschenaulti indicus.
Enicurus leschenaulti indicus Hartert, Vog. pal. Fauna, i. p. 760 (1910 — " Sikkim, Bhutan, Berglander
siidlich des Brahmaputra bis zum mittleren Tenasserim ").
Type: <$ ad., Margherita, Upper Assam, 19.i. 1902. H. N. Coltart leg.
NOVITATES ZOOLOGICAE XXVII. 1920. 475
649. Monticola rufocinerea sclateri Hart. = Monticola rufocinerea sclateri.
Monticola rufocinerea sclateri Hartert, Nov. Zool. 1917. p. 459 (Yemen and South Arabia).
Type : <$ ad., Wasil, Yemen, 4,000 feet, 4 . iii . 1913. G. W. Bury leg.
650. Monticola cyanus transcaspicus Hart. = Monticola solitarius transcaspicus .
Monticola cyanus transcaspicus Hartert, Bull. B.O. Club, xxiii. p. 43 (1909 — Tedjen, Sirax, Ashabad
in Transcaspia).
Type: $ ad., Sirax, 120 versts south of Tedjen, Transcaspia, 21. iii. 1905
(probably Russian date). Bought from Schliiter.
Distribution and characters require further study. The genus Monticola
(whether the Rock-Thrush and the Blue Rock-Thrush are united or separated
generically) stands distinctly between the Chats (Oenanthe) and Thrushes (Turdus),
but nearer the former.
651. Turdus colombianus Hart. & Hellm. = Turdus (obsoletus ?) colombianus.
Turdus colombianus Hartert & Hellmayr, Nov. Zool. viii. p. 492 (1901 — Cali, Western Colombia).
Type : <J, Cali, 18.ix. 1894. W. H. F. Rosenberg leg. No. 1.
I am by no means sure that this is a subspecies of obsoletus, though Chapman
(Distr. Bird-life, Colombia, p. 536) says it must be.
652. Turdus obsoletus parambanus subsp. nov.
Type : $ ad., Paramba, N.W. Ecuador, 3,500 feet, 23.vii. 1899. R. Miketta
leg. No. 477.
We have one male and two females from Paramba, collected in January,
July, and August ; also a male form from near Jimenez, W. Colombia, 2,900 feet,
collected by Merwyn G. Palmer, seems to belong to this form, and not to
colombianus !
These birds are closely allied to T. o. obsoletus from Costa Rica and Panama,
but the upperside is of a still deeper brown, the outer edges of the primaries are
darker, and the undersurface darker brown. Wings : <J, 120, 122 ; $ (worn),
about 118 mm.
I am inclined to think that obsoletus, parambanus, perhaps also colombianus,
nigrirostris, and hauxwelli are subspecies of jumigatus.
653. Turdus fumigatus caparo subsp. nov.
Type : <$, Caparo, Trinidad, 12. i v. 1902. E. Andre leg.
As already noticed by Hellmayr, Novitates Zoologicae, 1906, p. 4, Trinidad
specimens (one dozen compared with an equal number of Amazonian examples)
are much lighter and paler above and below than Brazilian ones, and there is
therefore no reason not to separate them ; many less recognizable subspecies
have been named recently from South America. Especially noticeable is the
paler, less rufescent upperside, and the lighter breast and sides. The skin from
Duaca mentioned by Hellmayr and two from the Orinoco are much nearer to
caparo, but seem to me to be intermediate.
476 NOVITATES ZOOLOOICAE XXVII. 1920.
654. Turdus ignobilis goodfellowi Hart. & Hellm. = Turdus ignobilis goodfellowii.
Turdus ignobilis goodfellowi Hartert & Hellmayr, Nov. Zool. viii. p. 492 (1901 — " Cauca Valley,
Colombia ").
Type : <J ad., Castilla, Cauca Valley, Colombia, vi.1898. J. H. Batty leg.
655. Turdus crotopezus contemptus Hellm. = Turdus crotopezus contemptus.
Turdus crotopezus contemptus Hellmayr, Journ.f. Orn. 1902. p. 61 (Bolivia, Peru).
Cotype : ? ad., Bueyes (St. Cruz), Bolivia, 21.iv.1890. Garlepp leg. Ex
Coll. Nehrkorn.
656. Turdus graueri Neum. = Turdus graueri.
Turdus graueri Neumann, Bull. B.O. Club, xxi, p. 56 (1908 — " Countries between the Kagera River
and Lake Kivu ").
Type: "?" ad., Nsasa, ll.vii.1907. Rud. Grauer leg. No. 732.
This bird is certainly not T. bocagei, which I consider a subspecies of pelios.
657. Turdus olivaceus bambusicola Neum. = Turdus olivaceus bambusicola.
Turdus olivaceus bambusicola Neumann, Bull. B.O. Club, xxi. p. 56 (February 1908 — " Western Kivu
Volcanoes ").
Type : $ ad., Bamboo Forest, Western Kivu Volcanoes, 2,300 m., 23. viii. 1907.
Rud. Grauer leg. No. 1,076.
658. Turdus citrinus aurimacula Hart. = Turdus citrinus aurimacula.
Turdus citrinus aurimacula Hartert, Nov. Zool. xvii. p. 236 (1910 — Hainan).
Type : cJ ad., Hoihow, Hainan, 13.iii. 1902. Katsumata leg.
659. Geocichla audacis Hart. = Turdus peronii audacis.
Oeocichla audacis Hartert, Bull. B.O. Club, viii. p. xliii. (1899 — Dammar or Dammer Island).
Type : $ ad., Wulur, Dammer, 4.xi.l898. Heinrich Kiihn leg. No. 983.
660. Geocichla dohertyi Hart. = Turdus dohertyi.
Oeocichla dohertyi Hartert, Nov. Zool. iii, p. 555. pi. xi. fig. 3 (" In insulis Lombok — typus — et
Sambawa dictis ").
Type : (J ad., Lombok, 5,000 feet, vi.1896. William Doherty leg.
661. Geocichla dumasi Rothsch. = Turdus dumasi.
Oeocichla dumasi Rothschild, Bull. B.O. Club, viii. p. 30 (1899— Burn).
Type : (J ad., Mt. Mada (Kapala Madang), Buru, viii. 1898. J. Dumas leg.
662. Merula celaenops yakushimensis Ogawa = Turdus celaenops jakushimensis.
Merula celaenops yakushimensis Ogawa, Annot. Zool. Japan, v. p. 180 (1905 — Yakushima, south of
Kiushiu).
Type: $ ad., Yakushima, 21.x. 1904. Collected by Owston's Japanese
collectors.
Novitates Zooloqicae XXVII. 1920. 477
663. Turdus deningeri Stres. = Turdus deningeri,
Turdus deningeri Stresemann, Bull. B.O. Club, xxxi. p. 4 (1912 — Cerain) ; Nov. Zool. xxi. 1914.
p. 133.
Type: <$ ad., Gunong Pinaia, Ceram, 7,500 feet, 16. viii. 1911. Erwin
Stresemann leg. No. 903.
L.c. the author has discussed the affinities of this interesting Thrush, which
may one day be regarded as a subspecies of J. fuliginosus (poliocephalits auct.)
and pritzbueri, though both differ considerably. T. canescens, supposed to have
come from Goodenough Island, we have never received ; possibly the locality
is incorrectly stated, as we have had two good collections from Goodenough
Island.
664. Turdus fuscater ockendeni Hellm. = Turdus fuscater ockendeni.
Turdus fuscater ockendeni Hellmayr, Bull. B.O. Club, xvi. p. 91 (1906 — " S.E. Peru ").
Type: <3 ad., Limbani, Carabaya, Peru, 9,500 feet, 21 . iii . 1904. G. O.
Ockenden leg. No. 675 a.
665. Turdus merula cabrerae Hart. = Turdus merula cabrerae Hart.
Turdus merula cabrerae Hartert, Nov. Zool. viii. p. 313^1901 — Canary Islands).
Type: $ ad., Mercedes, Tenerife, 21. ii. 1901. Curt Floericke leg. No. 1,250.
666. Turdus merula mauritanicus Hart. = Turdus merula mauritanicus.
Turdus merula mauritanicus Hartert, Nov. Zool. ix. p. 323 (Maroceo).
Type : <J ad., Mehuila (" Mhoiwla "), Maroceo, 3.ii. 1902. F. W. Riggenbach
leg.
667. Turdus philomelos clarkei Hart. = Turdus philomelos clarkei.
Turdus philomelos clarkei Hartert, Vog. pal. Fauna, i. p. 651 (1910 — British Isles).
Type : cj ad., Tring, 16. v. 1902. Ernst Hartert leg.
668. Phaeornis palmeri Rothsch. = Phaeornis palmeri.
Phaeornis palmeri Rothschild, Avifauna of Laysan, I. part ii. p. 67 (1893 — Kauai).
Type : $, Kauai, Sandwich Islands, 24. iii. 1891. H. C. Palmer leg. No. 926.
669. Minius gilvus tobagensis Dalmas = Mimus gilvus tobagensis.
Mimus gilvus tobagensis Dalmas, Mem. Soc. Zool. France, xiii. p. 134 (1900 — Tobago).
Type: Tobago, 25. xi. 1898. Count Dalmas leg. No. 45.
670. Mimus gilvus antillarum Hellm. & Seil. = Mimus gilvus antillarum.
Mimus gilvus antillarum Hellmayr & Seilern, Verh. Orn. Ges. Bayern, XII. part iii. p. 201 (1915 —
" Kleine Antillen ").
Type : cJ ad., Grenada, November 1897. P. Gellinau leg. Ex Coll. Dalmas.
31
478 Novitates Zoolooicae XXVII. 1920.
671. Nesomimus bindloei Ridgw. = Mimus melanotis bindloei.
Nescmtimus bindloei Ridgway, Proc. U.S. Nat. Mus. xvii. p. 358 (1894— Bindloe Island, Galapagos Is.).
Type : <$ ad., Bindloe Island, 5.ix. 1891. G. A. Baur leg. No. 690.
672. Nesomimus bauri Ridgw. = Mimus melanotis bauri.
Nesomimus bauri Ridgway, Proc. U.S. Nat. Mus. xvii. p. 357 (1894 — Tower Island, Galapagos).
Type: Ad., Tower Island, 2. ix. 1891. G. A. Baur leg. No. 695. (From
spirits !)
673. Nesomimus carringtoni Rothsch. = Mimus melanotis carringtoni .
Nesomimus carringtoni Rothschild, Bull. B.O. Club, viii. p. vii. (1898 — Barrington Island).
Type: <J ad., Barrington Island, 7.x. 1897. R. H. Beck leg. Webster-
Harris Expedition. No. 1,540.
(The name "carringtoni" was a misprint for barringtoni, but to avoid
confusion was never altered.)
674. Nesomimus hulli Rothsch. = Mimus melanotis hulli.
Nesomimus hulli Rothschild, Bull. B.O. Club, vii. p. liii. (1898— Culpepper Island, Galapagos).
Type : (J ad., Culpepper Island, 27. vii. 1897. R. H. Beck leg. Webster-
Harris Expedition. No. 166.
675. Nesomimus affinis Rothsch. = Mimus parvulus afjinis.
Nesomimus afjinis Rothschild, Bull. B.O. Club, vii. p. liii. (1898 — Narborough Island).
Type : £ ad., Narborough Island, 6.xii.l897. R. H. Beck leg. Webster-
Harris Expedition. No. 2,852.
676. Nesominus adamsi Ridgw. = Mimus adamsi.
Nesomimus adamsi Ridgway, Proc. U.S. Nat. Mus. xvii. p. 358 (1894 — Chatham Island).
Type : <$ ad., Chatham Island, 13. vi. 1891. G. A. Baur leg. No. 694.
677. Pteruthius tahanensis Hart. = Pteruthius melanotis tahanensis*
Pteruthius tahanensis Hartert, Nov. Zool. ix. p. 576 (1902— Gunong Tahan, Eastern Malay Peninsula,
Pahang).
Type : <$ ad., Gunong Tahan, x.1901. J. Waterstradt leg.
678. Herpornis xantholeuca interposita Hart. = Herpornis xantholeuca interposita.
Herpornis xantholeuca interposita Hartert, Bull. B.O. Club, xxxviii. p. 20 (1917— Malay Peninsula).
Type : Temangoh, Upper Perak, 24. vii. 1909. C. Boden Kloss leg.
679. Ixulus flavicollis harterti Har. = Ixulus flavicollis harterti ? f
Ixutus flavicollis harterti Harington, Bull. B.O. Club, xxxiii. p. 62 (1913—" The Bhamo Hills and
Trans-Salween Shan States, Burma ").
Type: $ ad., Sinlum, near Bhamo, 25. iv. 1908. H. H. Harington leg.
No. 232.
* The systematic position of Pteruthius is not clear. Probably it is here quite out of place.
f Perhaps the Bame as /. flavicollis rouxi (I. rouxi) Oustalet, Bull. Mus. Paris, 1896, p. 186,
from Yunnan, with which Harington did not compare it.
NoVITATES ZOOLOQICAE XXVII. 1920. 479
680. Siva strigula malayana Hart. = Siva strigula malayana.
Siva strigula malayana Hartert, Nov. Zool. ix. p. 567 (1902 — Mts. of Malay Peninsula).
Type : <J ad., Gunong Tahan, x.1901. J. Waterstradt leg.
681. Staphidia everetti Sharpe = Staphidia everetti.
Stapkidia everetti Sharpe, Ibis, 1887. p. 447 (Kina Balu, Borneo).
Type: $ ad., Kina Balu, 3,000 feet, 1 . iii . 1887. John Whitehead leg.
No. 1,044.
682. Brachypteryx poliogyna mindorensis Hart. = Brachypteryx poliogyna
mindorensis.
Bradypteryx poliogyna mindorensis Hartert, Bull. B.O. Club, xxxvi. p. 87 (1916 — Mindoro, Philippine
Is.).
Type : $ ad., Mt. Dulungan, Mindoro, 4,500 feet, 25. i. 1896. John White-
head leg. No. B 93.
683. Brachypteryx brunneiceps Grant = Brachypteryx poliogyna brunneiceps.
Brachypteryx brunneiceps Grant, Ibis, 1896. p. 547 (Negros).
Type of (J, Canloon Volcano, Negros, 27. iv. 1896. John Whitehead leg.
No. B 471. (Marked by the author " Type of #.")
684. Brachypteryx erythropyga Sharpe = Brachypteryx erythropyga.
Brachypteryx erythropyga Sharpe, Ibis, 1888. p. 389 (Kina Balu).
Type : $ ad., Kina Balu, N.E. Borneo, 8,000 feet, 27.ii. 1888. John White-
head leg. No. 2,084.
685. Brachypteryx floris Hart. = Brachypteryx floris.
Brachypteryx floris Hartert, Nov. Zool. iv. p. 170 (1897 — Flores).
Types : $ ?, ad., Flores, about 3,500 feet, October and November 1896.
Alfred Everett leg.
686. Myiophoneus borneensis Slat. = Myiophoneus borneensis.
Myiophoneus borneensis Slater, Ibis, 1885. p. 124 (described from one juvenile specimen from the
Bungal Hills, Borneo).
Type : Juv., Bungal Hills, near Sarawak, Borneo. Harvey leg. (Ex Coll.
H. H. Slater.)
687. Macronus kettlewelli Guill. = Macronus kettlewelli.
Macronus kettlewelli Guillemard, Proc. Zool. Soc. London, 1885. p. 262. pi. xviii. fig. 2 (Sulu Islands,
south of Philippine Islands).
Type: cj, Lukatlapas, Sulu Island, 18. v. 1883. H. Guillemard leg.
(Ml NoVITATES ZOOLOOICAE XXVII. 1920.
688. Macronus ptilosus reclusus Hart. = Macron us ptilosus reclusus.
Macronus ptilosus reclusus Hartert, Bull. B.O. Club, xxxvi. p. 36 (1915— Borneo).
Type : <J ad., Kina Balu, Borneo, 1,000 feet, 17.L1888. John Whitehead
leg. No. 1,881.
689. Mixornis cagayanensis Guill. = Mixornis montana cagayanensis.
Mixornis cagayanensis Guillemard, Proc. Zool. Soc. London, 1885. p. 419 (Cagayan, Sulu Islands).
Type : (J, Cagayan Sulu, l.iv.1883. H. Guillemard leg.
690. Mixornis montana Sharpe = Mixornis montana montana.
Mixornis montana Sharpe, Ibis, 1887. p. 448 (Kina Balu).
Type : Ad., Kina Balu. John Whitehead leg. No. 1,347.
691. Mixornis prillwitzi Hart. = Mixornis prillwitzi (or M. gularis prillwitzi).
Mixornis prillwitzi Hartert, Bull. B.O. Club, xii. p. 32 (1901— Kangean Island, N.E. of Java).
Type : (J ad., Kangean, September 1901. Ernst Prillwitz leg. No. 163.
692. Mixornis everetti Hart. = Mixornis everetti.
Mixornis everetti Hartert, Nov. Zool. i. p. 472 (1894 — Bunguran, Natuna Island) ; fig. Nod. Zool. ix.
Type: <J ad., Bunguran, 14.x. 1893. Alfred Everett leg.
693. Cyanoderma melanothorax baliensis Hart. = Cyanoderma melanothorax
baliensis.
Cyanoderma melanothorax baliensis Hartert, Bull. B.O. Club, xxxvi. p. 2 (1915— Bali).
Type : S ad., Bali, low country, March 1896. William Doherty leg.
694. StachyridopsisruficepsgoodsoniRothsch. = Stachyridopsis ruficeps goodsoni.
Stachyridopsis ruficeps goodsoni Rothschild, Bull. B.O. Club, xiv. p. 8 (October 1903— Hainan).
Type: <J ad., Mt. Wuchi, Hainan, 24. iii. 1903. Katsumata leg.
695. Stachyridopsis rafiirons ambigua Har. = Stachyridopsis rufifrons ambigua.
Stachyridopsis rufifrons ambigua Harington, Journ. Bombay Nat. Hist. Soc. xxiii. p. 631 (1915 —
Assam, Naga Hills, Manipur, probably to Butan Duars and Sikkiin).
Type: <J ad., Gunjong, North Cachar Hills, 26. xii. 1895. E. C. Stuart
Baker leg.
696. Stachyris leucotis goodsoni Hart. = Stachyris leucotis goodsoni.
Stachyris leucotis goodsoni Hartert, Bull. B.O. Club, xxxvi. p. 7 (1915— Borneo).
Type : Ad., Gunong Mulu, Sarawak, hi. 1898. John Waterstradt leg.
697. Stachyris guttata swinhoei Rothsch. = Stachyris guttata swinhoei.
Stachyris guttata swinhoei Rothschild, Bull. B.O. Club, xiv. p. 8 (October 1903—" Mt. Wuchi,
Hainan ").
Type : <J ad., Mt. Wuchi, Hainan, 28.iii. 1903. Katsumata leg.
Novitates Zoolooicae XXVII. 1920. 481
698. Stachyris nigriceps coltarti Har. = Stachyris nigriceps coltarti.
Stachyris nigriceps coltarti Harington, Bull. B.O. Club, xxxiii. p. 61 (November 1913 — " Dibrugarh
in Assam ; Naga and Chin Hills, and the Bhamo Hills ").
Type : $ ad., Margherita, Upper Assam, 4.xii.l901. H. N. Coltart leg.
699. Stachyris natunensis Hart. = Stachyris nigriceps natunensis.
Stachyris natunensis Hartert, Nov. Zool. i. p. 470 (1894 — Natuna Islands, Bunguran).
Type : $ ad., Bunguran, 5.x. 1893. Alfred Everett leg.
This form is very near S. n. davisoni, but differs by the less rufescent,
somewhat more olivaceous upperside.
700. Stachyris borneensis Sharpe = Stachyris nigriceps borneensis.
Stachyris borneensis Sharpe, Ibis, 1887. p. 449 (Mt. Kina Balu, Borneo).
Type : c? ad., Kina Balu, 25.iii.1887. John Whitehead leg.
701. Proparus brunnea argutus Hart. = Proparus brunneus argutus.
Proparus brunnea argutus Hartert, Nov. Zool. xvii. p. 231 (1910 — Hainan).
Type : <$ ad., Mt. Wuchi, Hainan, 25 . iii . 1903. Katsumata leg.
702. Alcippe collaris Walden = Proparus rufogularis.
Alcippe collaris Walden, Ann. & Mag. Nat. Hist. xiv. 1874. p. 156 (1874 — One single rj, Sadya,
Assam. Day leg.).
Type: <J ad., Sadiya, Upper Assam, 12. i . 1874. Day leg. (Bought with
the Elwes Collection.)
703. Proparus nipalensis rufescentior Hart. = Proparus tiipalensis rufescentior.
Proparus nipalensis rufescentior Hartert, Nov. Zool. xvii. p. 231 (1910 — Hainan).
Type : <J ad., Mt. Wuchi, Hainan, 28. iii. 1903. Katsumata leg.
704. Alcippe haringtoniae Hart. = Proparus poeocephalus haringtoniae.
Alcippe haringtoniae Hartert, Bull. B.O. Club, xxv. p. 10 (October 1909 — Bhamo, Upper Burma).
Type : <J ad., Bhamo, 29. iii. 1909. Colonel H. H. Harington leg.
705. Corythocichla crassa Sharpe = Turdinulus crassus.
Corythocichla crassa Sharpe, Ibis, 1889. p. 391 (Kina Balu).
Type : $ ad., Kina Balu, N. Borneo, 8,000 feet, 15. ii. 1888. John Whitehead
leg.
This is a typical Turdinulus.
| 706. Turdinulus humei Hartert = Turdinulus epilepidotus granti.
Turdinulus granti Richmond, Proc. U.S. Nat. Mus. xxii. p. 320 (1900 — Lower Siam).
Turdinulus humei Hartert, Nov. Zool. ix. p. 564 (1902 — Gunong Tahan, Eastern Malay Peninsula).
Type : <J ad., Gunong Tahan, 1,500 feet, September 1901. John Water-
stradt leg.
4S2 NoVITATES ZOOLOQICAE XX\1I. 1920.
707. Turdinulus exsul Sharpe = Turdinulus epilepidotus exsul.
Turdinulus exsul Sharpe, Ibis, 1888. p. 479 (Kina Balu).
Type : $ ad., Kina Balu, North Borneo, 4,000 feet, May 10th, 1888. John
Whitehead leg.
708. Turdinulus roberti hainanus Hart. = Turdinulus roberti hainanus.
Turdimdus roberti hainanus Hartert, Nov. Zool. xvii. p. 230 (1910 — Hainan).
Type : <$ ad., Mt. Wuchi, Hainan, 25. iv. 1903. Katsumata leg.
(?) f 709. Crateroscelis rufobrunnea R. & H. = Crateroscelis murina ?
Crateroscelis rufobrunnea Rothschild & Hartert, Bull. B.O. Club, xi. p. 25 (1900 — " Mt. Maori, a little
west of Humboldt Bay, in Dutch New Guinea ").
Type : Juv., Mt. Maori, west of Humboldt Bay, January 1899. J. Dumas
leg.
This is apparently the young of Crateroscelis murina, but our juveniles from
Southern Papua are not quite so dark, and the determination of subspecies of
this species is still in doubt.
710. Crateroscelis pectoralis Rothsch. & Hart. = Crateroscelis pectoralis.
Crateroscelis pectoralis Rothschild & Hartert, Bull. B.O. Club, xi. p. 25 (1900— Owen Stanley Range,
Mt. Cameron, etc.) (figured in Nov. Zool. 1901).
Type : £ ad., Mt. Cameron, Owen Stanley Range, S.E. New Guinea,
21 . viii. 1S96. A. G. Anthony leg.
711. Ptilopyga mindanensis Bias. = Ptilocichla mindanensis.
Ptilopyga mindanensis Blasius, Braunschweigische Anzeigen, No. 94, April 15, 1889, Journ. f. Orn.
1890. p. 146 (Mindanao) ; Ptilocichla (?) Mindanensis nov. spec. Steere, List B. Mamm. Exped.
Philippines, p. 18 (1889).
Type: J ad., Davao, Mindanao, 9. viii. 1889. Dr. C. Platen leg. (Ex-
changed from the late Mr. Nehrkorn.)
712. Malacopterum cinereum bungurense Hart. = Setaria cinerea bungurensis.
Malacopterum cinereum bungurense Hartert, Nov. Zool. i. p. 470 (1894 — Bunguran Island, Natuna
group).
Type : $ ad., Bunguran Island, 13.x. 1893. Alfred Everett leg.
[Setaria kalulongae (Sharpe) : " Cotype " and topotype, Mount Kalulong,
Borneo, February. Charles Hose leg. Marked " cotype " by the author— we
now call it para type.]
713. Erythrocichla bicolor whiteheadi Hart. = Erythrocichla bicolor whiteheads
Erythrocichla bicolor ivhiteheadi Hartert, Bull. B.O. Club, xxxvi. p. 36 (December 1915— North
Borneo).
Type : cj ad., Benkoker, North Borneo, 11.x. 1885. John Whitehead leg.
NOVITATES ZOOLOGICAE XXVII. 1920. 483
f 714. Ifrita coronata Rothsch. = Ifrita koivaldi.
Todopsis kowaldi De Vis, Report on B. from Brit. Neiv Guinea, p. 3 (1889 — Mts. Brit. New Guinea).
Ifrita coronata Rothschild, Bull. B.O. Club, vii. p. liv. (1898 — " Low country east of Port Moresby " ?
Probably wrong, inhabits only fairly high elevations in the mountains !) Figured : Nov. Zool.
1899. pi. iii. fig. 1.
Type : " Low country east of Port Moresby " — errore ! Must be Owen
Stanley Mts. Bought, apparently collected by some prospector or native.
Professor Oscar Neumann called my attention to the fact that Todopsis
kowaldi is an earlier name for Ifrita coronata. There is no doubt about it, but it
is inconceivable why, and a bad misjudgment to even compare Ifrita with the
genus Todopsis ! It makes study very difficult and causes loss of time and
errors if birds are described in entirely wrong genera.
715. Bathmocercus vulpinus Rchw. = Bathmocercus rufus vulpinus <J.
Bathmocercus vulpinus Reichenow, Nov. Zool. ii. p. 160 (1895 — Aruwimi River).
Type : <$ ad., Aruwimi River, Eastern Congo basin. W. Bonny leg.,
member of Stanley's Emin Pasha Relief Expedition (Rear Column).
f 716. Bathmocercus murinus Rchw. = Bathmocercus rufus vulpinus ?.
Bathmocercus murinus Reichenow, Nov. Zool. ii. p. 160 (1895 — Aruwimi River).
Type : $ ad., Aruwimi River. W. Bonny leg.
It is now well known that the greyish specimens are the females, the rufous
ones the males. Reichenow was in error when (Vog. Afr. iii. p. 742) he placed
B. jacksoni as a synonym of B. rufus rufus. B. jacksoni is, however, probably
a synonym of B. rufus vulpinus, but more Aruwimi specimens are desirable for
comparison. Specimens from west of Lakes Albert Edward and Tanganyika,
Toro, and North Kavirondo (Grauer, van Someren, and Meinertzhagen coll.)
agree inter se, and, I think, with the Aruwimi specimens, which, however, are
bad skins.
717. Ptyrticus turdinus Hartl. = Ptyrticus turdinus.
Ptyrticus turdinus Hartlaub, Zoolog. Jahrb. ii. p. 315 (1887 — Tomaja, Mombuttu).
Type : ? ad., Tomaja. Emin Pasha leg.
This very interesting bird remained unique, until it was rediscovered by the
late Boyd Alexander.
718. Lioptilus rufocinctus Rothsch. = Lioptilus rufocinctus.
Lioptilus rufocinctus Rothschild, Bull. B.O. Club, xxiii. p. 6 (October 1908 — Rugege forest, S.E. of
Lake Kivu).
Type : "$" ad., Rugege forest, S.E. of Lake Kivu, 16.xii.1907. Rudolf
Grauer leg.
t 719. Turdinus pyrrhopterus kivuensis Neum. = Malacocincla pyrrhoptera.
Turdinus pyrrhopterus kivuensis Neumann, Bull. B.O. Club, xxi. p. 55 (1908 — Kivu Volcanoes).
Type: "$" ad., Mt. Sabjingo, Kivu Volcanoes, 2,700 m., 30. viii. 1907.
Rudolf Grauer leg. No. 1,128.
484 NOVTTATES ZOOLOGICAE XXVII. 1920.
It is quite clear that Neumann, when describing his kivuensis, compared it
with immature specimens, which have the head less grey, more or less brown.
This is clearly shown by Dr. van Someren's splendid series.
720. Turdinus moloneyanus iboensis Hart. = Turdinus moloneyanus iboensis.
Turdinus moloneyanus iboensis Hartert, Bull. B.O. Club, xix. p. 84 (May 1907 — Oguta, in the Ibo
country, Southern Nigeria).
Type : J ad., Oguta, 19. xi. 1901. W. J. Ansorge leg. No. 400.
Turdinus phoebei Kemp, Bull. B.O. Club, xxi. p. Ill (June 1908), from the
same country, is a synonym of iboensis !
721. Turdinus ugandae van Someren = Turdinus fulvescens ugandae.
Turdinus ugandae van Someren, Bull. B.O. Club, xxxv. p. 125 (1915 — " Uganda forests ").
Type: $ ad., Sezibwa River, Chagwe province, Uganda, 16. xi. 1914.
Dr. V. G. L. van Someren leg. No. 169.
(We have probably an undescribed form, another subspecies of fulvescens, a
female from Canhoca, Angola, but it would perhaps be rash to describe it without
further material.)
722. Turdinus canicapillus Sharpe = Malacocincla pyrrhogenys canicapilla.
Turdinus canicapillus Sharpe, INs, 1887. p. 450 (Kina Balu, Borneo).
Type: J ad., Kina Balu, 3,000 feet, 25.iii.1887. John Whitehead leg.
No. 1,354.
723. Malacocincla sepiaria tardinata Hart. = Malacocincla sepiaria tardinata.
Malacocincla sepiaria tardinata Hartert, Bull. B.O. Club, xxxvi. p. 35 (1915 — " Eastern Malay
Peninsula").
Type : $ ad., Gunong Tahan, Eastern Malay Peninsula, 1,000 feet, November
1901. John Waterstradt leg.
724. Graueria vittata Hart. = Graueria vittata.
Graueria vittata Hartert, Bull. B.O. Club, xxiii. p. 8 (1908 — " High forest west of Lake Albert Edward
and Rugege Forest, S.E. of Lake Kivu ").
Type : <J, primeval forest, 90 kilometres west of Lake Albert Edward,
1,600 m., 8. ii. 1908. Rudolf Grauer leg. No. 1,987.
725. Macrosphenus flavicans ugandae van Someren = Macrosphenus flavicans
•ugandae.
Macrosphenus flavicans ugandae van Someren, Bull. B.O. Club, xxxv. p. 126 (1915 — "Uganda
forests ").
Type : <$ ad., Mabira Forest, 14. i. 1914. V. G. L. van Someren leg.
726. Pseudotharrhaleus caudatus Grant = Pseudotharrhaleus caudatus.
Pseudolluirrhaleus caudatus Grant, Bull. B.O. Club, iv. p. xl. (1895 — North Luzon).
Type : $ ad., Mt. Data, North Luzon, 7,500 feet, 25. i. 1895. John White-
head leg. No. A 48. (Specimen marked " Type of $.— J. W.")
Novttates Zoolooicaz XXVII. 1920. 485
727. Pseudotharrhaleus unicolor Hart. = Pseudotharrhaleus unicolor.
Pseudotharrhaleus unicolor Hartert, Bull. B.O. Club, xiv. p. 74 (April 1904 — Mt. Apo, Mindanao).
Type : $, Mt. Apo, 3,000 feet, November 1908. John Waterstradt leg.
No. 114.
(Mearns, Proc. Biol. Soc. Washington, xviii. p. 2, 1905, and Proc. U.S. Nat.
Mus. xxxvi. p. 441, 1909 — has described two other Pseudotharrhaleus from
Mindanao. Future research must show if this is correct. I am now convinced
that my unicolor might perhaps be a young bird, though fully grown. The
wing-measure is not 92-5, which was a typographical error for 62-5, and I now
measure it 63 mm. We know so far nothing of the changes of plumage in these
rare birds, but if my unicolor is in its juvenile garb, then Mearns's griseipectus
may be expected to be the adult of it, and thus a synonym. Cf. Ibis, 1906,
p. 479. Possibly Ps. malindangensis Mearns is its northern representative on
the island. The greater size is not worth much as a distinguishing character.
I measure the wing of the male of P. caudatus as 65, that of the female as 63 mm.,
showing that the sexes differ slightly in size.)
728. Androphilus accentor Sharpe = Androphilus accentor.
Androphilus accentor Sharpe, Ibis, 1888. p. 390 (Kina Balu, N. Borneo).
Type: <J ad., Kina Balu, 8,000 feet, 3 . ii . 1888. John Whitehead leg.
No. 1,939.
f 729. Androphilus everetti Hart. = A ndrophilus castaneus castaneus.
Androphilus everetti Hartert, Nov. Zool. iii. p. 69 (1896 — Indrulaman, Bonthain Peak, S. Celebes).
[Turdinus castaneus Biittikofer, Notes Leyden Mus. xv. 1893. p. 261 (N. Celebes).]
Type : $ ad., Indrulaman, October 1895. Alfred Everett leg.
730. Androphilus disturbans Hart. = Androphilus castaneus disturbans.
Androphilus disturbans Hartert, Nov. Zool. vii. p. 238 (1900 — Mt. Mada, Buru).
TyPe : 6 l'uv> Mt- Madang, 3,000 feet, September 1898. J. Dumas leg.
The young bird was not fit to show the real affinities, but Stresemann obtained
an adult female from Mt. Fogha, 4.500 feet high, on Buru, which proves to my
mind that disturbans is a subspecies of A. castaneus.
731. Androphilus disturbans museums Stres. = Androphilus castaneus musculus.
Androphilus disturbans musculus Stresemann, Nov. Zool. xxi. p. 136 (1914 — Middle and West Ceram).
Type: $ ad., Goonoong Pinaia, Middle Ceram, 7,500 feet, 18. viii. 1911.
Erwin Stresemann leg. No. 875.
732. Androphilus viridis Rothsch. & Hart. = Androphilus viridis.
Androphilus viridis Rothschild & Hartert, Bull. B.O. Club, xxix. p. 33 (1911— Mt. Goliath).
Type : $ ad., Mt. Goliath, eastern part of Snow Mountains Range in Central
Dutch New Guinea, 9.ii. 1911. A. S. Meek leg. No. 5,346.
So far only this one specimen of this striking species is known.
486 Novitates Zoolooioae XXVII. 1920.
(?) 733. Argya shaipii Ogilvie-Grant & Reid = Crateropus rubiginosus sharpii ?.
Argya sharpii Ogilvie-Grant & Reid, Ibis, 1901. p. 662 (Shebelli).
Type : <$ ad., Shebelli, 27.viii. 1894. Dr. A. Donaldson Smith leg. No. 201.
Though much larger, this specimen agrees in other ways perfectly with
Crateropus (Argya) rubiginosus rubiginosus, and it was rash to describe it as
" new species " from this one specimen. Without further material it cannot
be ascertained whether this is a distinct subspecies or an exceptionally large
specimen.
734. Crateropus caudatus altirostris Hart. = Crateropus (Argya) altirostris.
Crateropus caudatus altirostris Hartert, " Vog. pal. Fauna, p. 623 (1909 — "An der Nordspitze dea
Persischen Golfs, au der Miindung des vereinigten Euphrat und Tigris ").
Type : Fao, 1893. W. D. Cumming leg.
Though very much like C. (Argya) caudatus hitttoni, this form must be regarded
as a separate species, because a form of C. caudatus occurs together with it, in
the same region.
735. Crateropus plebeius kikuyuensis Neum. = Crateropus plebeius kikuyuensis.
Crateropus plebeius kikuyuensis Neumann, Orn. Monatsber. 1906. p. 7 (" Kikuyu ").
Type : $ ad., Escarpment station, Kikuyu Mts., February 1901, 6,500 feet.
William Doherty leg.
This form is very closely allied to C. p. emini Neum. from " Uniamwesi,
Lander am Tanganyka, Tabora, Usagara," but is slightly darker. It is also
close to C. p. hypostictus from Angola, but the latter is distinctly lighter in colour.
736. Crateropus smithi lacuum Neum. = Crateropus levcopygius lacuum.
Crateropus smithi lacuum Neumann, Bull. B.O. Club, xiv. p. 15 (1903 — " The Lake Valley south of
Shoa, from Lake Zuai to Lake Gandjule, and the mountain-slopes east of that valley ").
Type: S a(i.> Alelu, north of Lake Abassi, 9.xii.l900. Oscar Neumann
leg. No. 331.
737. Crateropus smithi omoensis Neum. = Crateropus leucopygius omoensis.
Crateropus smithi omoensis Neumann, Bull. B.O. Club, xiv. p. 15 (1903 — " The countries of the Omo
System — Uba, Gofa, Doko, Malo, and Kaffa, and also the head-waters of the Gelo River, Binescho
and Schecho ").
Type: J ad., Senti River between Uba and Gofa, 30. i. 1901. Oscar
Neumann leg. No. 713.
(Cf. also Journ. f. Orn. 1904, p. 553, 1906, pp. 261, 262.)
C. I. lacuum is nearest to C. I. smithi and stands between the latter and
omoensis, but is constant and well distinguishable from both. Only one specimen
of C. I. lacuum, No. 391, approaches C. I. omoensis.
738. Crateropus tenebrosus Haiti. = Crateropus tenebrosus.
Crateropus tenelirosus Hartlaub, Journ. f. Orn. 1883. p. 425 (Kudurma) ; id. Zool. Jahrb. 1897. p. 313.
Type: $ ad., Kudurma, S.E. Bahr-el-Ghazal, 10. xi. 1882. Emin Pasha
leg. No. 260.
NOVTTATES ZOOLOGICAE XXVII. 1920. 487
Neumann, Journ. f. Orn. 1904, p. 552, says : " Diese Art ist sicher der
geographische Vertreter des C. melanops." I am not so sure about this, and
should like to leave the question open. C. tenebrosus is still extremely rare. All
specimens known in collections are four in number : the type in Tring ; 2 speci-
mens collected by Donaldson Smith at Fort Berkeley ; 1 Mt. Baginzi, Bahr-el-
Ghazal, Christy leg. Mr. Butler (cf. Ibis, 1918, p. 695) says that it is " quite
a common bird in the vicinity of Kajo Kaji, in the Lado Enclave," but he does
not seem to have collected a single specimen.
739. Cataponera turdoides Hart. = Cataponera turdoides.
Cataponera turdoides Hartert, Nov. Zool. iii. p. 70 (1896 — Bonthain Park, South Celebes).
Type : $ ad., Bonthain Peak, 6,000 feet, October 1895. Alfred Everett leg.
740. Garrulax schistochlamys Sharpe = Garrulax schistochlamys.
Garrulax schistochlamys Sharpe, Ibis, 1888. p. 479 (Kina Balu, North Borneo).
Type: J ad., Kina Balu, 15. v. 1888. John Whitehead leg. No. 2,538.
741. Allocotops calvus Sharpe = Allocotops cahnis.
Allocotops calvus Sharpe, Ibis, 1888. p. 389 (Kina Balu).
Type: <J ad., Kina Balu, North Borneo, 4,000 feet, 27. iii. 1888. John
Whitehead leg. No. 2,321.
742. Trochalopteron canorum owstoni Rothsch. = Ianthocincla (Trochalopteron)
canorum owstoni.
Trochalopteron canorum oxostoni Rothschild, Bull. B.O. Club, xiv. p. 8 (1903 — Hainan).
Type : ? ad., Mt. Wuchi, Hainan, 29. iii. 1903. Katsumata leg.
743. Ianthocincla lineatum grisescentior Hart. = Ianthocincla (Trochalopteron)
lineatum grisescentior.
Ianthocincla lineatum grisescentior Hartert, Vog. pal. Fauna, i. p. 636 (1909 — " Westlicher Himalaya :
Kamaon, Simla, bis Kaschmir in Hohen von 5,000 — 8,000 engl. Fuss ").
Type: Ad., Simla, 15. xi. 1880. H. J. Elwes leg. No. 1,548.
744. Ianthocincla lineatum gilgit Hart. = Ianthocincla (Trochalopteron) lineatum
gilgit.
Ianthocincla lineatum gilgit Hartert, Vog. pal. Fauna, i. p. 636 (1909 — " Hohe Berge des nord-
ostlicheren Kaschmir." This is a misprint or penslip for " nordwestlichen," as Gilgit is in
north-west Kashmir !).
Type : $ ad., Gilgit, 3.ii. 1880. J. Scully leg.
745. Trochalopteron phoeniceum bakeri Hart. = Ianthocincla (Trochalopteron)
phoeniceum, bakeri.
Trochalopteron phoeniceum bakeri Hartert, Bull. B.O. Club, xxiii. p. 10 (1908 — " Mountain Ranges
south of the Brahmaputra ").
Type : £ ad., Laisung, North Cachar Hills, 23. ii. 1896. E. C. Stuart Baker '
leg. No. 32,960.
488 NoVITATES ZOOLOGICAE XXVII. 1920.
746. Ianthocincla affinis oustaleti Hart. = Ianthocincla (Trochalopteron) affinis
ousted eti.
Ianthocincla affinis oustaleti Hartert, Vog. pal. Fauna, i. p. 633 (1909 — Yunnan).
Type : Ad., Tsekou, Yunnan. Father Soulie leg. No. 349.
Confirmed by a series from the Likiang Range. Cap more blackish, back
less rufescent, underside more greyish, less rufescent.
748. Ianthocincla rufogularis assamensis Hart. = Ianthocincla rufogularis
assamensis.
Ianthocincla rufogularis assamensis Hartert, Vog. pal. Fauna, i. p. 635 (1909 — "Assam: Patkai-
Khasia- und Garo-Berge ").
Type : <J ad., Margherita, 12. i. 1902. Dr. H. N. Coltart leg. No. 12,102.
749. Ianthocincla rufogularis occidentalis Hart. = Ianthocincla rufogularis
occidentalis.
Ianthocincla rufogularis occidentalis Hartert, Vog. pal. Fauna, i. p. 635 (1909 — " Nordwestlicher
Himalaya von Kumaon bis Kaschmir ").
Type : Ad., Dehra Dun, Kashmir, ex Coll. Marshall. No. 11,109.
750. Pomatorhinus tickelli hainanus Rothsch. = Pomatorhinus tickelli hainanus.
Pomatorhinus tickelli hainanus Rothschild, Bull. B.O. Club, xiv. p. 9 (1903 — Hainan).
Type: <$ ad., No-tai, Hainan, 30. ix. 1902. Katsumata leg. No. 90a.
751. Pomatorhinus schisticeps fasbdiosus Hart. = Pomatorhinus schisticeps
jastidiosus.
Pomatorhinus schisticeps fastidiosus Hartert, Bull. B.O. Club, xxxvi. p. 81 (1916 — Trang and Kao
Nong, Bandon, Northern Malay Peninsula).
Type : J ad., Trang, 8. i. 1910. Ex Mus. Selangor.
752. Pomatorhinus schisticeps cryptanthus Hart. = Pomatorhinus schisticeps,
cryptanthus.
Pomatorhinus schisticeps cryptanthus Hartert, Bull. B.O. Club, xxxvi. p. 35 (1915 — " Hills south of
Brahmaputra, Cachar to Patkoi Hills ").
Type : <J ad., Margherita, Upper Assam, 22. ii. 1902. H. N. Coltart leg.
753. Eupetes castanonotus saturatus R. & H. = Eupetes castanonotus saturatus.
Eupetes castanonotus saturatus Rothschild & Hartert, Orn. Monatsber. xix. p. 157 (1911 — Snow
Mountains, New Guinea).
Type : <$, Snow Mountains of New Guinea, 2,000 feet, 24.viii. 1910. Albert
S. Meek Coll. No. 4,624.
754. Cinclosoma alisteri Math. = Cinclosoma alisteri.
Cinclosoma alisteri Mathews, Bull. B.O. Club, xxvii. p. 16 (1910— West Australia).
Type : <J ad., Waddilinia, W. Australia, 22. ix. No. 9,929.
Novitates Zoolooicae XXVII. 1920. 489
t 755. Bradyornis muscicapinus Hartl. = Muscicapa striata striata.
Bradyornis muscicapinus Hartlaub, Abhandl. nat. Ver. Bremen, xii. p. 9 (1891 — • Bagamoyo, E. Africa).
Type : $ ad., Bagamoyo. Emin Pasha leg.
(Of. Bull. B.O. Club, xxxiii. p. 65.)
f 756. Hemichelidon cinereiceps Sharpe = Muscicapa (H ' emichelidon) ferruginea.
Hemichelidon cinereiceps Sharpe, Ibis, 1887. p. 441 (Kina Balu, Borneo).
Type: Kina Balu, 26. ii. 1887. John Whitehead leg. No. 1,032.
757. Alseonax murinus djamdjamensis Neum. = Muscicapa (Alseonax) murina
djamdjamensis.
Alseonax murinus djamdjamensis Neumann, Journ. f. Orn. 1905. p. 206 (Djamdjam).
Type: $, Gerbitscho, Djamdjam, about 2,800 m., 14.xii.1900. Oscar
Neumann leg. No. 411.
758. Muscicapa ansorgei Hart. = Muscicapa (Alseonax) ansorgei.
(Perhaps subspecies of griseogularis.)
Muscicapa ansorgei Hartert, Bull. B.O. Club, xxv. p. 95 (May 1910 — Ogowe River, Gaboon).
Type : §, Ugowo, Ogowe River, Gaboon, 27.viii. 1907. W. J. Ansorge leg.
No. 722.
759. Muscicapa reichenowi Neum. = Muscicapa (Dioptrornis) chocolatinus
reichenowi.
Muscicapa reichenowi Neumann, Orn. Monatsber. 1902. p. 10 (one specimen near Budda, in Gimirra,
west of Kaffa).
Type: (J ad., Budda, Gimirra, 17. iv. 1901. Oscar Neumann leg. No. 1,129.
This form requires confirmation. The type specimen is in badly worn
plumage, but it seems indeed to be much darker than M. (D.) ch. chocolatinus.
It can, however, not be more than a subspecies of the latter.
760. Dioptrornis semicinctus Hart. = Muscicapa (Dioptrornis) semicinctus.
Dioptrornis semicinctus Hartert, Bull. B.O. Club, xxxvii. p. 4 (1916 — Kabakaba, Eastern Congo
Free State).
Type: $ ad., Kabakaba, North-Eastern Congo Free State, 5.ix.l906.
C. F. Camburn leg. No. 408.
This is also known, so far, from a single specimen only, but it appears to be
a perfectly distinct species.
761. Muscicapa toruensis Hart. = Muscicapa (Dioptrornis) toruensis.
Muscicapa toruensis Hartert, Nov. Zool. 1900. p. 37 (Toru, Uganda Protectorate).
Type : $ ad., Fort Gerry, Toru, 9.iv. 1899. W. J. Ansorge leg. No. 351.
Besides the type from Toru we have now 16 skins, all collected by Grauer
in the Kivu region, Rugege forest, west and north-west of Lake Tanganyika,
Kwidjwi Island, near Lake Albert Edward and Baraka. The young is darker
490 Novitates Zoolooicae XXVII. 1920.
on the back and spotted with white, while the feathers of the underside have
blackish edges.
762. Microeca flavigaster laetissima Rothsch. = Microeca flavigasler laetissima.
Microeca flavigaster laetissima Rothschild, Bull. B.O. Club, xxxvii. p. 4 (1916— Queensland).
Type : $ ad., Cardwell, Queensland.
763. Microeca oscillans Hart. = Microeca oscillans.
Microeca oscillans Hartert, Nov. Zool. 1897. pp. 170. 524 (South Flores).
Type : £ ad., South Flores, about 3,500 feet. Alfred Everett leg.
764. Microeca addita Hart. = Microeca addita.
Microeca addita Hartert, Nov. Zool. 1900. p. 234 (" Mount Mada, 3,000 feet high ").
Type : c? ad.. Mount Madang, Buru, August — September 1898. J. Dumas
leg.
765. Microeca griseiceps occidentalis R. & H. = Microeca griseiceps occidentalis.
Microeca griseiceps occidentalis Rothschild & Hartert, Nov. Zool. 1903. p. 471 (" Warmendi,'' Arfak).
Type: "Warmendi," Arfak, 24. i. 1876, " <?." From Bruijn's hunters.
No. B 124.
This bird is undoubtedly different from M. g. griseiceps, but so far we know
only this one specimen.
f 766. Microeca viridiflava Rothsch. & Hart. = Microeca papuana.
Microeca papuana Meyer, Sitzungsber. Ges. Isis, 1875. p. 74 (Arfak).
Microeca viridiflava Rothschild & Hartert, Bull. B.O. Club, xi. pp. 26. 44 (1900— Mt. Cameron).
Type: $ ad., Mt. Cameron, 6,500 feet, 1 .viii. 1896. A. S. Anthony leg.
(Fig. Nov. Zool. 1901.)
(This is probably a subspecies of Microeca hypoxantka Scl. from Tenimber
[Timorlaut], of which we have one of the typical specimens collected by H. O.
Forbes. )
767. Muscicapa narcissma jakuschima Hart. = Muscicapa (Zanthopygia)
narcissina jakuschima.
Muscicapa narcissina jakuschima Hartert, Vog. d. pal. Fauna, p. 491 (1907 — Yaku Island, south of
Kiu-shiu).
Type: £ ad., Yaku-shima (Yaku I.), 18.x. 1904. No. 1,064. Collected
by Alan Owston's Japanese birdskinners.
768. Stoparola panayensis nigriloris Hart. = Eumyias panayensis nigriloris.
Stoparola panayensis nigriloris Hartert, Bull. B.O. Club, xiv. p. 80 (1904 — Mt. Apo, Mindanao).
Type : ^ ad., Mt. Apo, 3,000 feet, October 1908. John Waterstradt leg.
(We have also paratypes of Grant's Stoparola nigrimentalis, rectius S. pana-
yensis nigrimentalis, from North Luzon.)
NOVITATES ZOOLOGICAE XXVII. 1920. 491
769. Stopai'ola panayensis obiensis Hart. = Eumyias panayensis obiensis.
Sloparola panayensis obiensis Hartert, Bull. B.O. Club, xxxi. p. 2 (1912 — Obi Major).
Type : <J ad., Obi Major, 2,000 feet, 26. iv. 1902. John Waterstradt leg.
770. Stoparola cerviniventris Sharpe = Eumyias indigo cerviniventris.
Stoparola cerviniventris Sharpe, Ibis, 1887. p. 444 (Borneo).
Type : $ ad., Kina Balu, Borneo, 3,000 feet, 11 .iii. 1887. John Whitehead
leg. No. 1,094.
771. Siphia omissa Hart. = Cyornis banyumas omissa.
Siphia omissa Hartert, Nov. Zool. iii. p. 171 (1896 — Bonthain Peak, S. Celebes).
Type : J ad., Indrulaman, Bonthain Peak, September 1895. Alfred Everett
leg.
772. Cyornis banyumas peromissa subsp. nov.
Differs from C. r. omissa by its paler upperside and shorter wings. Wings :
cj, 72, 72, 73 ; $, 69 mm. (Against <J, 75, 76-5, 79 ; and $ 72 and 73-5 in C. r.
omissa !) The blue patch on the sides of the chest is also less developed than in
omissa ; and in the $ the bright-blue superciliary line is obsolete, while the
small feathers above and below the eye are more rufous.
Type : $ ad., Selayer, south of Celebes, November 1895. Alfred Everett
leg.
773. Siphia djampeana Hart. = Cyornis banyumas djampeana.
Siphia djampeana Hartert, Nov. Zool. iii. p. 172 (1896 — Djampea Island).
Type : £ ad., Djampea, December 1895. Alfred Everett leg.
774. Siphia kalaoensis Hart. = Cyornis banyumas kalaoensis.
Siphia kalaoensis Hartert, Nov. Zool. iii. p. 172 (1896 — Kalao Island).
Type : cJ ad., Kalao, December 1895. Alfred Everett leg.
One is tempted to distinguish two species, one with the female brown,
another with blue upperside, but considering the very great similarity of the
males of some forms I treat all these birds as subspecies of banyumas, which is
the oldest name of the group.
I would thus recognize the following forms known to me :
Cyornis banyumas banyumas (Horsf.), Java.
,, ,, rufigastra (Raffl.), Sumatra.
This bird has apparently not been found again and the type is not in the
British Museum ! It was supposed to be the same as banyumas, but, considering
that every other island has different forms, it is much more probable that the
Sumatran form is also different ! Recent collectors have not procured this
species at all. It is also possible that rufigastra was caeruleata, which is apparently
the older name of nigrigularis ; we have received a skin of this latter species
said to have been shot in Palembang, S.E. Sumatra, by a Mr. Volcker.
Cyornis banyumas dialilaema (Salvad.). Apparently Malay Peninsula and
Burmese provinces.
492 NOTITATES ZOOLOOICAE XXVII. 1920.
Cyornis banyumas rufifrons Wall., Borneo.
omissa (Hart.), S. Celebes.
peromissa Hart., Saleyer.
djampeana (Hart.), Djampea.
kalaoensis (Hart.), Kalao.
philippinensis Sharpe, Philippines.
According to Finsch (1901) simplex would be the older name for " philip-
pinensis," but as the type had no locality, this requires further confirmation !
C. b. omissa is of course not the same as C. banyumas banyumas, as Finsch
said. Not only can the males be distinguished, but the female of banyumas has
a brown upperside, that of omissa a blue one.
775. Cyornis hyacintliina kiihni Hart. = Cyornis hyacinthina kiihni.
Cyornis hyacinthina kiihni Hartert, Nov. Zool. 1904. p. 204 (Wetter Island).
T3T>e : <J ad., Wetter, 24. ix. 1902. Heinr. Kiihn leg. No. 5,467.
776. Siphia erithacus Sharpe = Cyornis erithacus.
Siphia erithacus Sharpe, Ibis, 1888. p. 199 (Palawan).
Type: <J ad., Taguso, Palawan, 26. vi. 1887. John Whitehead leg. No.
1,438.
777. Siphia bonthaina Hart. = Cyornis bonthaina.
Siphia bonthaina Hartert, Nov. Zool. 1896. p. 157 (Bonthain Peak, South Celebes).
Type : <J ad., Tasoso, Bonthain Peak, 4,000 feet, October 1895. Alfred
Everett leg.
778. Siphia innesa Swinh. = Muscicapa (Dendrobiastes) hyperythra innexa.
Siphia innexa Swinhoe, Ibis, 1886. p. 394 (a unique specimen, Formosa).
Type : $ ad., Formosa, 7. i. 1866. Swinhoe Coll.
779. Muscicapula hyperythra audacis Hart. = Muscicapa (Dendrobiastes)
hyperythra audacis.
Muscicapula hyperythra audacis Hartert, Nov. Zool. 1906. p. 296 (Babber, S.W. Islands).
Type : $ ad., Tepa, Babber, 6.ix. 1905. H. Kiihn leg. No. 6,864.
780. Muscicapula hyperythra pallidipectus Hart. = Muscicapa (Dendrobiastes)
hyperyth ra pallidipect us.
Muscicapula hyperythra pallidipectus Hartert, Nov. Zool. 1903. p. 52 (Batjan).
Type : $ ad., Batjan, 5—7,000 feet, vii. 1902. John Waterstradt leg.
781. Dendrobiastes hyperythra negroides Stres. = Muse. (Dendrob.) hyperythra
negroides.
Dendrobiastes hyperythra negroides Stresemann, Nov. Zool. 1914. p. 125 (Seran).
Type of $: Gunong Hoale, Ceram, 4. vii. 1911. Erwin Stresemann leg.
No. 692.
NOVITATES ZOOLOGICAE XXVII. 1920. 493
(Stresemann, I.e., said : Typen <$ G. Pinaia, No. 880, $ G. Hoale, No. 692,
but the male cannot be found now and has unaccountably been lost ; there are,
however, four other adult males in the collection.)
782. Dendrobiastes hyperythra alifurus Stres. = Muse. (Dendr.) hyperythra
alifura.
Dendrobiastes hyperythra alifurus Stresemann, Nov. Zool. six. p. 330 (1912 — Buru).
Type, as stated by the author : $, Gunong Fogha, Buru, 5,000 feet,
26. ii. 1912. Erwin Stresemann. No. 1,076.
783. Muscicapula nigrorum Whiteh. = Muse. (Dendr.) luzoniensis nigrorum.
Muscicapula nigrorum Whitehead, Bull. B.O. Club, vi. p. xliii. (1897 — Negros, in the Philippines).
Type: (J ad., Negros, Canloan Volcano, 6,700 feet, 23. iv. 1896. John
Whitehead leg. No. B 457.
784. Dammeria henrici Hart. = Muscicapa (Dendrobiastes) henrici.
Dammeria henrici Hartert, Bull. B.O. Club, viii. p. lviii. (1899— Damrner Island, in the Banda Sea).
Type : cJ ad., Kumar, Dammer, 13. xi. 1898. Heinr. Kiihn leg. No. 1,038.
785. Erythromyias buruensis Hart. = Erythromyias buruensis buruensis.
Erythromyias buruensis Hartert, Bull. B.O. Club, viii. p. 31 (1899— Buru).
Type : ^ ad., " Mt. Mada," Buru, 3,000 feet, September 1898. J. Dumas
leg.
t 786. Cryptolopha waigiuensis Hart. = Gerygone neglecta neglecta.
Gerygone neglecta Wallace, Proc. Zool. Soc. London, 1865. p. 475 (" Waigiou ; Mysol." Waigiu
restricted terra typica, Mysol not correct).
Cryptolopha waigiuensis Hartert, Bull. B.O. Club, xiii. p. 70 (1903 — Waigiu).
Type : $, Waigiu, 15.xii.1902. John Waterstradt leg.
This, though really Wallace's neglecta;, is by no means a typical Gerygone.
(See footnote, Nov. Zool., 1903, p. 473 !)
t 787. Gerygone neglecta dohertyi R. & H. = G. neglecta virescens.
" Sylvia virescens S. Mull." Blyth, Ibis, 1870. p. 169 footnote (" New Guinea ").
Pseudogerygone virescens Pinsch, Notes Leyden Museum, xx. p. 135 (1898 — Lobo Bay, Salomon
Miiller Coll.).
Gerygone neglecta dohertyi Rothschild & Hartert, Nov. Zool. x. p. 473 (1903 — Kapaur, 8 specimens).
Type : Kapaur, New Guinea, January 1897. William Doherty leg.
788. Gerygone rosseliana Hart. = Gerygone rosseliana rosseliana.
Gerygone rosseliana Hartert, Nov. Zool. 1899. p. 79 (Rossel Island, Louisiade group).
Type : S, Rossel Island, 5.ii.l898. A. S. Meek leg. No. 1,382.
32
494 NOVITATES ZOOLOGICAE XXVII. 1920.
789. Gerygone rosseliana onerosa Hart. = Gerygone rosseliana onerosa.
Gerygone rosseliana onerosa Hartert, Nov. Zool. vi. p. 209 (1899 — St. Aignan, Louisiade group).
Type : <$, St. Aignan Island, 5.ix. 1897. A. S. Meek leg. No. 964.
790. Gerygone magnirostris tagulana R. & H. = Gerygone magnirostris tagitlana.
Gerygone magnirostris tagulana Rothschild & Hartert, Nov. Zool. xxv. p. 318 (1918 — Sudest Islaud,
or Tugula, Louisiada group).
Type : ^ ad., Mt. Riu or Rattlesnake, Sudest Island, 20. iv. 1916. Eichhorn
Bros. leg. No. 7,565 of the Meek collections.
791. Gerygone magnirostris proxima R. & H. = Gerygone magnirostris proximo,.
Gerygone magnirostris proxima Rothschild & Hartert, Nov. Zool. xxv. p. 319 (1918 — Fergusson
Island, d'Entrecasteaux group).
Type : cJ» Fergusson Island, 3. i. 1895. A. S. Meek leg. No. 1.
792. Gerygone ktihni Hart. = Gerygone inornata kiihni.
Gerygone kiihni Hartert, Nov. Zool. 1900. p. 15 (Dammer Island).
Type: rj ad., Dammer, 13.x. 1898. H. Kiihn leg. No. 1,065.
793. Gerygone kisserensis sequens Hart. = Gerygone inomata sequens.
Gerygone kisserensis sequens Hartert, Nov. Zool. 1904. p. 205 (Romah Island).
Type: <J ad., Romah, 15.viii. 1902. H. Kiihn leg. No. 5,299a.
794. Gerygone everetti Hart. = Gerygone inornata everetti.
Gerygone everetti Hartert, Nov. Zool. 1897. p. 267 (Savu and Timor. Terra typica restricta Savu !
Timor errore !)
Type : & Savu Island, near Timor, August 1896. Alfred Everett leg.
795. Miro daimeiaerdi Rothsch. = Miro traversi ddnnefaerdi.
Miro dannefaerdi Rothschild, Nov. Zool. i. p. 688 (1894 — Snares Islands).
Type : cJ ad., Snares Islands, south of New Zealand. Dannefaerd leg.
| 796. Poecilodryas cyanus salvadorii R. & H = Poecilodryas cyana
subcyanea.
Poecilodryas cyanus salvadorii Rothschild & Hartert, Bull. B.O. Club, xi. p. 26 (1900 — Mts. Scratchley,
Cameron, etc.).
Poecilodryas subcyanea De Vis, Ibis, 1897. p. 377 (S.E. New Guinea).
Type : <J ad., Mt. Cameron, 7,000 feet, 15. viii. 1896. A. S. Anthony leg.
f 797. Poecilodryas nigriventris Hart. = Poecilodryas vicaria.
Poecilodryas vicaria De Vis, Annual Report Brit. New Guinea, 1890 to 1891, Appendix CC. p. 94
(1892— Mount Suckling).
Poecilodryas nigriventris Hartert, Bull. B.O. Club, xix. p. 51 (1907— Lower Mambare River).
Type: J ad., Lower Mambare River, 5. v. 1906. Albert S. Meek leg.
No. A 2,813.
NOVITATES ZOOLOGIC4E XXVII. 1920. 495
This species does not seem to occur on the southern side of the Owen-Stanley
Mountains, but, besides from the Mambare River, we have now specimens from
the Aicora River and from the Sattelberg.
798. Poecilodryas albonotata griseiventris R. & H. = Poecilodryas albonotata
griseiventris.
Poecilodryas albonotata griseiventris Rothschild & Hartert, Nov. Zool. xx. p. 496 (1913 — Mount
Goliath).
Type : $ ad., Mount Goliath, in the eastern continuation of the " Snow
Mountains " of New Guinea, 14. i. 1911. A. E. Meek Coll. No. 5,454.
799. Poecilodryas leucops nigro-orbitalis R. & H. = Poecilodryas (Tregellasia)
leuco/3S nigro-orbitalis.
Poecilodryas leucops nigro-orbitalis Rothschild & Hartert, Arov. Zool. xx. p. 497 (1913 — Snow Moun-
tains).
Type: <$ ad., Snow Mountains, 3,000 feet, 20.x. 1910. A. S. Meek Coll.
No. 4,862.
800. Poecilodryas leucops albigularis R. & H. = Poecilodryas (Tregellasia) leucops
albigidaris.
Poecilodryas leucops albigularis Rothschild & Hartert, Nov. Zool. xiv. p. 459 (1907 — Cape York,
North Queensland).
Type : $ ad., Cape York, 21 . vii. 1898. A. S. Meek's assistant leg. No. 1,992
of the Meek Collections.
801. Parisoma blanfordi distincta Hart. = Parisoma blanfordi distincta.
Parisoma blanfordi distincta Hartert, Nov. Zool. 1917. p. 459 (S. Arabia).
Type : <$ ad., Gerba, S. Arabia, 15.xi. G. W. Bury leg. No. 511.
802. Chloropeta natalensis major Hart. = Chloropeta natalensis major.
Chloropeta natalensis major Hartert, Bull. B.O. Club, xiv. p. 73 (1904 — Angola).
Type: Canhoca, Angola, 23.xii.1903. W. J. Ansorge leg. No. 1,545.
803. Diaphorophyia graueri Hart. = Diaphorophyia graueri.
Diaphorophyia graueri Hartert, Bull. B.O. Club, xxiii. p. 7 (1908 — Primeval forest, 90 kilometres west
of Lake Albert Edward).
Type : £ ad., primeval forest, 90 kilometres west of Lake Albert Edward,
1,600 m, 11. ii. 1908. Rudolf Grauer leg. No. 2,011.
804. Diaphorophyia ansorgei Hart. = Diaphorophyia ansorgei.
Diaphorophyia ansorgei Hartert, Bull. B.O. Club, xv. p. 74 (1905 — Benguella).
Type : $ ad., Cabeca de Ladroes, Benguella, 29. vii. 1904. W. J. Ansorge
leg. No. 467.
496 Novitates Zoolooicae XXVII. 1920.
805. Platysteira cyanea aethiopica Neum. = Platysteira cyanea aethiopica.
Plalysleira cyanea aethiopica Neumann, Journ. f. Orn. 1905. p. 210 (" Schoa und Siid-Athiopien ").
Type : <J ad., Banka, in Malo, 15. ii. 1901. Oscar Neumann leg. No. 807.
806. Pseudocalyptomena graueri Rothsch. = Pseudocalyptomena graueri.
Pseudocalyptomena graueri Rothschild, Ibis, 1909. p. 690. pi. x. (50 miles west of Russisi).
Type : (J, 50 miles west of Russisi, north of Lake Tanganyika, November
1908, 2,000 m. in bamboo forest. Rudolf Grauer leg. No. 3,956.
807. Smithornis capensis medianus Hart. & Som. = Smithornis capensis medianus.
Smithornis capensis medianus Hartert & van Someren, Bull. B.O. Club, xxxvi. p. 59 (1916 — " Kyambu
Forest, Uganda, Toro, and forests west of Lakes Albert Edward and the northern portion of
Tanganyika ").
Type : $ ad., Kyambu Forest, in Uganda, 10. x. 1915. V. G. L. van Someren
leg.
808. Smithornis capensis albigularis Hart. = Smithornis capensis albigularis.
Smithornis capensis albigularis Hartert, Bull. B.O. Club, xiv. p. 73 (1904 — Canhoca, North Angola).
Type : <$ ad., Canhoca, 23. xi. 1903. W. J. Ansorge leg. No. 1,332.
809. Hypothymis azurea oberholseri Stres. = Hypothymis azurea oberholseri.
Hypothymis azurea oberholseri Stresemann, Nov. Zool. xx. p. 295 (1913 — Formosa).
Type: J ad., Sharaikisha, Formosa, 5.iv. 1907. Collected by Alan Owston's
Japanese collectors.
810. Hypothymis azurea symmixta Stres. = Hypothymis azurea symmixta.
Hypothymis azurea symmixta Stresemann, Xov. Zool. xx. p. 294 (1913 — Lombok, Sumbawa, Flores,
Alar).
Type : $ ad., Alor, March 1897. Alfred Everett leg.
811. Hypothymis puella blasii Hart. = Hypothymis puella blasii.
Hypothymis puella blasii Hartert, Nov. Zool. v. p. 131 (1898 — Sula Mangoli and Sula Besi Islands).
Type : (J, Sula Besi, November 1897. William Doherty leg.
812. Rhipidura sumbensis Hart. = Rhipidura rufi/rons sumbensis.
Rhipidura sumbensis Hartert, Nov. Zool. iii. p. 585 (1896 — Sumba).
Type : <$ ad., Sumba Island, February 1896. William Doherty leg.
813. Rhipidura louisiadensis Hart. = Rhipidura rufifrons louisiadensis.
Rhipidura louisiadensis Hartert, Nov. Zool. vi. p. 78 (1899 — Louisiades, Rossel Island).
Type : <J ad., Rossel Island, 30. i. 1398. A. S. Meek leg. No. 1,335.
NOVITATES ZOOLOQICAE XXVII. 1920. 497
814. Rhipiduia saipanensis Hart. = Rhipidura rufifrons saipanensis.
Rhipidura rufifrons saipanensis Hartert, Nov. Zool. v. p. 54 (1898 — Saipan, Marianne Islands).
Type: $ ad., Saipan, 1 . viii . 1895. Collected by Alan Owston's Japanese
skinners.
815. Rhipidura superflua Hart. = Rhipidura rufifrons superfiua.
Rhipidura superfiua Hartert, Bull. B.O. Club, viii. p. 32 (1899 — Buru).
Type : <J, Mount Madang (" Mada "), Buru, 3,000 feet, September 1898.
Dumas leg.
816. Rhipidura rufiventris pallidiceps Hart. = Rhipidura rufiventris pallidiceps.
Rhipidura rufiventris pallidiceps Hartert, Nov. Zool. xi. p. 205 (1904 — Wetter Island, near Timor).
Type : <J ad., Wetter, 16. ix. 1902. Heinr. Kiihn leg. No. 5,511.
817. Rhipidura rufiventris tiandu subsp. nov.
While in R. rufiventris rufiventris, pallidiceps, and assimilis the chest is pale
brownish grey and the white spots have a somewhat washed-out appearance,
not being in so sharp a contrast, in the new subspecies the chest is darker, more
slate-grey, and the white spots stand out bolder, in sharp contrast ; moreover,
the crown of the head is darker, more blackish, and the ear-coverts almost pure
black. The tips of the lateral rectrices are purer white. The dimensions are
the same.
Type: $ ad., Taam Island, in the Tiandu group, 25.vii.1899. Heinrich
Kiihn leg. No. 1,349.
Of Rh. rufiv. tiandu I have now 12 specimens from Taam, Kilsuin, and Kur
in the Tiandu or Kur group, stretching from Tenimber to Ceram (Seran). I had
long ago noticed these differences, but the distribution seemed so very improbable,
as we have 21 specimens, indistinguishable, so far as I am able to make out, from
Add, near Great and from Little Key, as well as from Kisui and Teoor in the
Watubela group, north of the Tiandu Islands. But the difference of the new
subspecies is so striking that I cannot hesitate any longer, but herewith give it
a name. Perhaps the Tiandu group, for reasons unknown to us, has been peopled
with its birds in another way than the Watubela Islands.
818. Rhipidura setosa niveiventris R. & H. = Rhipidura rufiventris niveiventris.
Rhipidura setosa niveiventris Rothschild & Hartert, Bull. B.O. Club, xxxiii. p. 109 (1914 — Admiralty
Islands).
Type: <J ad., Manus, Admiralty Islands, 13.ix.1913. Eichhorn Bros. leg.
A. S. Meek Expeditions, No. 6,053.
819. Rhipidura setosa nigromentalis Hart. = Rhipidura rufiventris nigromentalis.
Rhipidura setosa nigromentalis Hartert, Nov. Zool. v. pp. 525, 526 (1898 — Sudest and St. Aignan
Islands).
Type : <$ ad., Sudest Island, Louisiade group, 13. iv. 1898. A. S. Meek leg.
No. 1,7 21.
498
NOVTTATES ZOOLOGICAE XXVII. 1920.
820. Rhipidura nigrocinnamomea Hart. = Rhipidura nigrocinnamomea.
Rhipidura nigrocinnamomea Hartert, Bull. B.O. Club, xiv. p. 12 (1903— Apo Volcano, Mindanao).
Type : <J ad., Apo Volcano, Mindanao, 8,000 feet, April 1903. Walter
Goodfellow leg. No. 137.
821. Rhipidura cockerelli septentrionalis R. & H. = Rhipidura cockerelli
septentrionalis.
Rhipidura cockerelli septentrionalis Rothschild & Hartert, Bull. B.O. Club, xxxvi. p. 73 (1916 —
Bougainville Island).
Type : "$" ad., Bougainville Island, Solomon group, 11 . xii. 1912. A. S.
Meek leg. No. 3,537.
822. Rhipidura cockerelli interposita R. & H. = Rhipidura cockerelli
inter posita.
Rhipidura cockerelli interposita Rothschild & Hartert, Bull. B.O. Club, xxxvi. p. 73 (1916 — Isabel
Island).
Type: "$" ad., Isabel Island, Solomon group, 4.vii.l901. A. S. Meek
leg. No. 3,494.
823. Rhipidura cockerelli lavellae R. & H. = Rhipidura cockerelli lavellae.
Rhipidura cockerelli lavellae Rothschild & Hartert, Bull. B.O. Club, xxxvi. p. 74 (1916— Vella Lavella
Island).
Type: "?" ad., Vella Lavella Island, Solomons, 1 . iii . 190S. A. S. Meek
leg. No. 3,902.
824. Rhipidura albina R. & H. = Rhipidura cockerelli albina.
Rhipidura cockerelli albina Rothschild & Hartert, Nov. Zool. 1901. p. 183 (Kulambangra).
Type: $ ad., Kulambangra Island, Solomon group, 13. iii. 1901. A. S.
Meek leg. No. 2,872.
More specimens must be collected on Kulambangra, where only this one
was obtained, to show finally whether the Rendova specimens (cf. Nov. Zool.
1905, p. 260) are exactly the same as the Kulambangra form.
825. Rhipidura atra Salvad. = Rhipidura atra.
Rhipidura atra Salvadori, Ann. Mus. Civ. Genova, viii. p. 922 (1875 — Arfak, New Guinea).
Cotype : <$ ad., Hatam, Arfak, 28. vi. 1875. Collected by Bruijn's hunters.
Specimen e of Salvadori's list in Orn. Papuaria Molucc. Marked in the author's
handwriting : " e Rhipidura atra Salvad. nov. sp. Typus ! " It is according
to modern nomenclature a cotype, as all specimens were marked " Typus."
826. Callaeops periophthalmica Grant = Tchitrea periophthalmica.
Callatops periophtlmlmica Ogihuc-Grant, Bull. B.O. Club, iv. p. xviii. (1895 — Luzon).
Type : " <J," bought in Manila by the late John Whitehead, said to have
been killed with a blow-pipe near Manila.
NOVITATES ZOOLOGIOAE XXVII. 1920. 499
In Nov, Zool. xxiii. pp. 335-336, pi. i. 1916, I have given a brief history
of what I then supposed to be the unique specimen of this rare bird. I was,
at the time, not aware that the bird described by Mr. McGregor in the
Philippine Journal of Science, ii. A, No. 5, pp. 340-342, from Batan Island, north
of Luzon, where he found it to be common, was the same. The possibility of
this has been suggested in the Manual of Philippine Birds, 2, p. 467, but I agree
with Richmond (Auk, xxxiv. pp. 216, 217, 1917), that certainly the two birds
are the same, and also that I was in error in maintaining the genus Callaeops,
which in reality cannot be separated from Tchitrea. This extraordinary species
must therefore be called Tchitrea periophthalmica (Grant), and is no longer unique,
though the only specimen in any European Museum, so far, is the type. If
the statement of the native was correct, that it was killed near Manila, its
occurrence there must have been quite exceptional, its real home being Batan
Island, between Luzon and Formosa.
827. Tchitrea cambumi Neum. = Tchitrea camburni.
Tchitrea camburni Neumann, Ball. B.O. Club, xxi. p. 43 (1908 — Ituri Forest).
Type: " <J," Ituri Forest, "Congo Free State," ll.vii.1906. C. F.
Camburn leg. No. 299.
This was the only specimen obtained by the collector.
828. Tchitrea paradisi borneensis Hart. = Tchitrea parodist borneensis.
Tchitrea paradisi borneensis Hartert, Bull. B.O. Club, xxxvi. p. 75 (1916 — Sarawak, Borneo).
Type : (J ad., Bejalong, Sarawak, vi.1903. Brook leg.
829. Philentoma dubium Hart. = Philentoma pyrrhopterwm dubium.
Philentoma dubium Hartert, Nov. Zool. i. p. 477 (1894 — Bunguran, Natuna Islands).
Type : <J, Bunguran Island, 6.x. 1893. Alfred Everett leg.
830. Rhinomyias pectoralis baliensis Hart. = Rhinornyias umbratilis
baliensis.
Rhinomyias pectoralis baliensis Hartert, Nov. Zool. iii. p. 549 (1896 — Bali).
Type : $, Bali, March— April 1896. William Doherty leg.
831. Rhinomyias ruficrissa Sharpe = Rhinomyias ruficrissa.
Rhinomyias ruficrissa Sharpe, Ibis, 1887. p. 441 (Kina Balu, Borneo).
Type: $, Kina Balu, 3,000 feet, 4. iii. 1887. John Whitehead leg. No. 1,061.
832. Rhinomyias colonus Hart. = Rhinomyias colonus.
Rhinomyias colonus Hartert, Nov. Zool. v. p. 131 (1898 — Sula Mangoli, east of Celebes).
Type : (J, Sula Mangoli, November 1897, William Doherty leg.
833. Rhinomyias gularis Sharpe = Rhinomyias gularis.
Rhinomyias gularis Sharpe, Ibis, 1888. p. 385 (Kina Balu, Borneo).
Type: ?, Kina Balu, 7,000 feet, 27. iii. 1888. John Whitehead leg. No.
2,323.
500 NOVTTATES ZOOLOQIOAE XXVII. 1920.
834. Culicicapa ceylonensis sejuncta Hart. = Culicicapa ceijlonensis sejuncta.
Culicicapa ceylonensis sejuncta Hartert, Nov. Zool. iv. p. 526 (1897 — South Flores).
Type : <J, South Flores, October 1896. Alfred Everett leg.
835. Myiagra rubecula papuana R. & H. = Myiagra rubecula papuana.
Myiagra rubecula papuana Rothschild & Hartert, Nov. Zool. xxv. p. 317 (1918 — British New Guinea).
Type: ^ ad., Kumusi River, N.E. British New Guinea, 28. vii. 1907. A. S.
Meek leg. No. 3,322.
836. Myiagra rubecula sciurorum R. & H. = Myiagra rubecula sciurorum.
Myiagra rubecula sciurorum Rothschild & Hartert, Nov. Zool. xxv. pp. 316. 318 (1918 — Rossel and
Sudest Islands).
Type : $ ad., Rossel Island, 3. hi. 1898. A. S. Meek leg. No. 1,352.
837. Myiagra feminina R. & H. = Myiagra jerrocyanea feminina.
M yiagra feminina Rothschild & Hartert, Nov. Zool. viii. p. 183 (1901 — Kulambangra Island, Solomon
group).
Type : ?, Kulambangra, 8 . iii . 1901. A. S. Meek leg. No. 2,850.
f 83S. Myiagra nupta Hart. = Myiagra cyanoleuca (Vie ill.).
Myiagra nupta Hartert, Nov. Zool. 1898. p. 526 (Sudest Island).
Type : <$ ad., Sudest Island, 16. iv. 1898. A. S. Meek leg. No. 1,738. (Cf.
Nov. Zool. 1918, p. 316 !)
839. Myiagra rufigula colonus Hart = Myiagra ruficollis colonus.
if yiagra rufigula colonus Hartert, Nov. Zool. iv. p. 266 (1897 — Djampea and Kulao, south of Celebes).
Type : $ ad., Djampea, December 1895. Alfred Everett leg.
840. Myiagra galeata buruensis Hart. = Myiagra galeata buruensis.
if yiagra galeata buruensis Hartert, Nov. Zool. 1903. p. 9 (Buru).
Type : <J ad., Kayeli, Buru, October 1898. Alfred Everett leg.
841. Myiagra galeata seranensis St res. = Myiagra galeata seranensis.
if yiagra galeata seranensis Stresemann, Nov. Zool. xxi. p. 127 (1914 — Seran [Ceram]).
Type: $ ad., Manusela, Ceram, 9.vi.l911. Erwin Stresemann leg. No.
595.
842. Machaerirhynchus flaviventer novus R. & H. = Machaerirhynchus flaviventer
novus.
Machaerirhynchus flaviventer novus Rothschild & Hartert, Nov. Zool. xix. p. 200 (1912 — Kumusi
River and Collingwood Bay, British New Guinea).
Type: ^ ad., Haidana, Collingwood Bay, 15. iv. 1907. A. S. Meek coll.
No. 2,839.
Novitates Zoological XXVII. 1920. 501
843. Machaerirhynchus nigripectus saturatus R. & H. = Machaerirhynchus
nigripectus saturates.
Machaerirhynchus nigripectus saturatus Rothschild & Hartert, Nov. Zool. xx. p. 498 (1913 —
Mt. Goliath).
Type : ? ad., Mt. Goliath, 2 . ii . 1911. A. S. Meek coll. No. 5,276.
(Mr. Ogilvie-Grant, Ibis, Jubilee Suppl. 2, 1915, p. 144, doubted the dis-
tinctness of saturatus from harterti of British New Guinea, but the two forms
are easily distinguishable, if series are compared.)
844. Cryptolopha burkii valentini Hart. = Cryptolopha burkii valentini.
Cryptolopha burkii valentini Hartert, Vog. pal. Fauna, i. p. 497 (1907—" Siid-Kansu und Schensi ;
Tsin-ling Gebirge, im Waldgiirtel ").
Type: $ ad., Taipaishan, Tsin-ling Mts., 2.vi.l905. Collected by Alan
Owston's Japanese collectors. No. 13,205.
845. Cryptolopha mindanensis Hart. = Cryptolopha mindanensis .
Cryptolopha mindanensis Hartert, Bull. B.O. Club, xiv. p. 12 (1903— Mt. Apo, Mindanao).
Type : $, Mt. Apo, Mindanao, 8,000 feet, April 1903. Walter Goodfellow
leg.
When I described this species, I had only the one specimen, but it has since
been collected by Mearns.
846. Cryptolopha montis Sharpe = Cryptolopha montis tnontis.
Cryptolopha montis Sharpe, Ibis, 1887. p. 442 (Kina Balu, Borneo).
Type: <J ad., Kina Balu, 4,000 feet, 25. ii. 1887. John Whitehead leg.
No. 1,017.
847. Cryptolopha xanthopsia Whitehead = Cryptolopha montis xanthopygia.
Cryptolopha xanthopygia Whitehead, Bull. B.O. Club, i. p. xxxi. (1893— "Hab. in montibus insulae
Palawanensia ").
Type: $ ad., Palawan, 1,500 feet, 4.viii.l887. John Whitehead leg.
No. 1,642.
I consider this form undoubtedly to be a subspecies of C. montis ; the latter
has no yellow on the rump, C. montis floris a narrow, C. m. xanthopygia a wide
yellow rump-band. The bill of xanthopygia is rather longer than thicker than
that of C. m. montis.
848. Cryptolopha montis floris Hart. = Cryptolopha montis floris.
Cryptolopha montis floris Hartert, Nov. Zool. iv. p. 171 (1897— South Flores).
Type : <J ad., South Flores, above 3,500 feet, November 1896. Alfred
Everett leg.
849. Cryptolopha butleri Hart. = Cryptolopha castaneiceps butleri.
Cryptolopha butleri Hartert, Bull. B.O. Club, vii. p. I. (1898—" Gunong Ijau, 4,000 feet ").
Type: $ ad., Gunong Ijau, Perak, Malay Peninsula, iii.1898. A. L.
Butler leg.
502 Novitates ZoOtOGIOAE XXVII. 1920.
In view of the subspecies of C. montis I do not now hesitate to treat this as
a subspecies of castaneiceps, another subspecies of which is C. castaneiceps sinensis.
850. Cryptolopha budongoensis Seth-Smith = Cryptolopha budongoensis.
Cryptolopha budongoensis Seth-Smith, Bull. B.O. Club, xxi. p. 12 (1907 — " Budongo Forest, Uganda
Protectorate ").
"Types": <J, 25. ii. 1907; $, 20. v. 1907, Budongo Forest. L. M. Seth-
Smith leg.
f 851. Abrornis sakaiorum Stres. = Abrornis superciliar.is schwaneri aberr.
Abrornis sakaiorum Stresemann, Bull. B.O. Club, xxxi. p. 27 (1912 — " Upper Batang-Padang Valley,
3,000 feet ").
Type and unique specimen: <J, Batang-Padang Valley, Perak, 1.x. 1910.
Erwin Stresemann leg. No. C 25.
Evidently a colour- variety of A. superciliaris schivaneri as suggested by
Stresemann in litt.
852. Monarcha cinerascens rosselianus R. & H. = Monarcha cinerascens
rosselianus.
Monarcha cinerascens rosselianus Rothschild & Hartert, Nov. Zool. xxiii. p. 297 (1916 — Rossel Island).
Type: $ ad., Rossel Island, Louisiade group, 6. ii. 1898. A. S. Meek leg.
No. 1,385.
853. Monarcha everetti Hart. = Monarcha everetti.
Monarcha everetti Hartert, Nov. Zool. iii. p. 173 (1896 — Djampea).
Type : $ ad., Djampea in the Flores Sea, south of Celebes, December 1895.
Alfred Everett leg.
854. Monarcha kulambangrae R. & H. = Monarcha kulambangrae kulam-
bangrae.
Monarcha kulambangrae Rothschild & Hartert, Nov. Zool. 1901. p. 183 (Kulambangra Island).
Type : S ad., Kulambangra, Solomon Islands, 12. iii. 1901. A. S. Meek leg.
No. 2,868.
855. Monarcha chalybeocephalus manumudari R. & H. = Monarcha chalybeoceph.
manumudari.
Monarcha chalybeocephalus manumudari Rothschild & Hartert, Nov. Zool. xxii. p. 43 (1915 — Vulcan
Island).
Type : $ ad., Vulcan or Manumudar Island, north coast of Kaiser Wilhelm's
Land, 4.xii.l913. Eichhorn Bros. leg. A. S. Meek's expeditions, No. 6,358.
856. Monarcha kulambangrae meeki R. & H. = Monarcha kulambangrae meeki.
Monarcha kulambangrae meeki Rothschild & Hartert, Nov. Zool. 1905. p. 262 (Rendova Island).
Type: <$ ad., Rendova, Solomon Islands, 23. ii. 1904. A. S. Meek leg.
No. A 1,355.
NOVITATES ZOOLOGICAE XXVII. 1920. 503
857. Monarcha brodiei floridana R. & H. = Monarcha brodiei floridanus.
Monarcha brodiei floridana Rothschild & Hartert, Nov. Zool. 1901. p. 182 (Florida Island).
Type: c? ad., Florida, Solomon Islands, 4. i. 1901. A. S. Meek leg. No.
2,740.
858. Monarcha brodiei nigrotectus Hart. = Monarcha brodiei nigrotectus.
Monarcha brodiei nigrotectus Hartert, Bull. B.O. Club, xxi. p. 107 (1908 — Vella Lavella Island).
Type: c? ad., Vella Lavella Island, Central Solomon Islands, 8 . iii. 1908.
A. S. Meek Coll. No. 3,957.
859. Monarcha castaneiventris megarhynchus R. & H. = Monarcha castaneiventris
megarhynchus.
Monarcha castaneiventris megarhynchus Rothschild & Hartert, Nov. Zool. xv. p. 363 (1908 — San
Christoval Island).
Type : $ ad., Yanuta, San Christoval Island, Solomon Islands, 26. iv. 1908.
A. S. Meek Coll. No. 4,089.
f 860. Pomarea ribbei Hart. = Pomarea erythrosticta.
Pomarea erythrosticta Sharpe, Proc. Zool. Soc. London, 1888. p. 185 (Fauro Island).
Pomarea ribbei Hartert, Nov. Zool. 1895. p. 485 (Munia Island).
Type : $ ad., Munia Island, Shortland group, in the Solomon Archipelago,
27. ix. 1893. Wahnes & Ribbe leg.
(Munia is very near Fauro. The specimens with white crescent in front of
the eyes and larger size are the males, those with the rufous crescent and smaller
dimensions the females !)
FRUNELLIDAE ACCENTORIDAE ).
861. Prunella collaris ripponi Hart. == Prunella collaris ripponi.
Prunella collaris ripponi Hartert, Vog. pal. Fauna, i. p. 766 (1910 — " Von den hohen Bergenostlich
von Tali — Talifu — im westlichen Jiinnan ").
Type : Ad., Gyi-dziu-shan, east of Talifu, 10,000 feet, 5.iv.l902. Col. G.
Rippon leg.
862. Accentor erythropygius Swinh. = Prunella erythrypygia.
Accentor erythropygius Swinhoe, Proc. Zool. Soc. London, 1870. p. 124. pi. ix. (" On my journey back
from Mongolia to Peking, in the Prefecture of Seuen-hwafoo, 26th September, 1868, at a place
called Kemeih," ..." we secured one " out of a small flock).
Type : J ad., Kemeih, 26. ix. 1868. R. Swinhoe leg.
863. Accentor modularis occidentalis Hart. = Prunella modularis occidentalis.
Accentor modularis occidentalis Hartert, Brit. B. iii. p. 313 (1910 — " British Isles ").
Type : <J ad., Tring, 10. iv. 1893. Ex Coll. N. C. Rothschild.
504 Novitates Zooloqicae XXVII. 1920.
TROGLODYTIDAE.
f 864. Cinclus cinclus sardus Hart. = Cinclus cinclus sapsworthi.
Cinclus cinclus sapsworthi Arrigoni, Atlante Ornitologico, p. 150 (1902 — Corsica).
Cinclus cinclus sardus Hartert, Bull. B.O. Club, xiv. p. 51 (1904 — Sardinia).
Type : (J ad., near Ogliastro, Sardinia, 14. xi. 1902.
865. Cinclus cinclus hibernicus Hart. = Cinclus cinclus hibernicus .
Cinclus cinclus hibernicus Hartert, Vog. pal. Fauna, i. p. 790 (1910 — -Ireland).
Type: <J, County Cork, Ireland, 25.viii. 1896. Bought from Brazenov
Bros. No. 2,598.
866. Hydrobata marila Swinh. = Cinclus pallasii marila.
Hydrobata marila Swinhoe, Journ. North China Branch R. Asiat. Soc. No. 2. p. 227 (1859 — Formosa).
Type (marked in Swinhoe's handwriting " Type of Hydrobata marila, Swinh.").
$ ad., Formosa, 24. vi. 1858. R. Swinhoe leg. No. 175.
f 867. Cinclus bilkevitchi Zar. = Cinclus cinclus leucogaster Bp.
Cinclus bilkevitchi Zarudny, Orn. Jahrb. xiii. p. 57 (1902 — Descr. of one <J ad., Tau-Tekele, Altai,
16.(28.)vii. 1894).
Type : ^ ad., Tau-Tekele, Altai Mts. 16. vi. 1894, Russian date (= 28. vi. 1894,
erroneously vii. in Orn. Jahrb.). S. Bilkevitch leg. Ex Coll. Zarudny.
868. Troglodytes troglodytes islandicus Hart. = Troglodytes troglodytes islandicus.
Troglodytes troglodytes islandicus Hartert, Bull. B.O. Club, xxi. p. 25 (1907 — Iceland).
Type : <J ad., Gilsbakki, Iceland, 13. vi. 1900. H. H. Slater leg. No. 3,690.
869. Troglodytes troglodytes kabylorum Hart. = Troglodytes troglodytes
kabylorum.
Troglodytes troglodytes kabylorum Hartert, Vog. pal. Fauna, i. p. 870 (1910 — Atlas).
Type : <$ ad., near Alger, 25. ii. 1909. Rothschild, Hartert, and Hilgert leg.
No. 8.
870. Troglodytes troglodytes szetschuanus Hart. = Troglodytes troglodytes
szetschuanus.
Troglodytes troglodytes szetschuanus Hartert, Vog. pal. Fauna, i. p. 783 (1910 — Tsinling Mts., Sechuan
to Ichang).
Type : <S, Mu-kua-chi, Lung-an, Sechuan, 15. v. 1893 (Russian date). Bere-
zowsky leg.
871. Troglodytes troglodytes taivanus Hart. Troglodytes troglodytes taivanus.
Troglodytes troglodytes taivanus Hartert, Vog. pal. Fauna, i. p. 776 (1910 — Formosa).
Type : <J ad. , Mt. Arizan, Formosa, 1 3 . xii . 1 906. Collected by Alan O wston's
Japanese collectors.
Novitates Zoologicae XXVII. 1920. 505
872. Cistothorus platensis tucumanus Hart. = Cistothorus platensis tucumanus.
Cistothorus platensis tucumanus Hartert, Nov. Zool. 1909. p. 163 (Tucurnan, Argentina).
Type : $ ad., Tucuman, 30.x. 1899. J. Venturi leg.
873. Cistothorus platensis meridae Hellm. = Cistothorus platensis meridae.
Cistothorus platensis meridae Hellmayr, Bull. B.O. Club, xix. p. 74 (1907 — Merida, Venezuela).
Type : Ad., El Loro, Andes of Merida, 3,000 m., 13.viii. 1898. Sal. Briceiio
Gabaldon e hijos leg.
874. Thryothorus genibarbis intercedens Hellm. = Thryothorus genibarbis
intercedens.
Thryothorus genibarbis intercedens Hellmayr, Nov. Zool. 1908. p. 17 (Goyaz, Brazil).
Type : (J ad., Rio Thesouras, state of Goyaz, 600 m., May 1906. G. A. Baer
leg. No. 2,167.
875. Thryothorus griseipectus caurensis Berl. & Hart. = Thryothorus griseipectus
caurensis.
Thryothorus griseipectus caurensis Berlepsch & Hartert, Nov. Zool. ix. p. 7 (1902 — Caura River,
Orinoco region, Venezuela).
Type : cJ ad., Nicare, Caura River, 12. i. 1901. E. Andre leg.
876. Thryothorus goodiellowi Scl. = Thryothorus goodfellowi.
Thryothorus goodfellowi Selater, Bull. B.O. Club, xi. p. 47 (1901 — " Aequatoria oecidentalia ").
Type: $ ad., Papallacta, Eastern Ecuador, 11,500 feet, February 1899.
Goodfellow and Hamilton leg.
877. Thryophilus albipectus hypoleucus Berl. & Hart. = Thryophilus albipectus
hypoleucus.
Thryophilus albipectus hypoleucus Berlepach & Hartert, Nov. Zool. ix. p. 6 (1902 — Altagraeia on the
Orinoco).
Type : c? ad., Altagraeia, 6. i. 1898. Geo. K. Cherrie Collection. No. 9,550.
878. Odontorhynchus branickii minor Hart. = Odontorhynchus branickii minor.
Odontorhynchus branickii minor Hartert, Bull. B.O. Club, xi. p. 40 (1900 — Paramba, N. Eouador).
Type : (J, Paramba, 3,500 feet, 21 . iii . 1899. G. Flemming leg.
506 Novitates Zoolooicae XXVII. 1920.
A NOTE ON THE TYPE-LOCALITY AND GEOGRAPHICAL
RACES OF THE GUNDI (CTENODACTYLUS GUNDI
ROTHM.)
BY OLDFIELD THOMAS.
AMONG M. Blanc's Mammals from S. Tunis there are two skins of Gundis,
and these are so much more vivid and warm in colour than those we
have had from Biskra and elsewhere that they would seem to be worthy of
subspecific distinction from the better-known form. But the first consideration
was as to the type-locality of Rothmann's original Mus gundi, which has been
quoted as " Masuffin, Atlas Mountains," the village " Masuffin " not being
identifiable, and the " Atlas Mountains " having been simply assumed to be the
comparatively high Atlas mountains of Algeria or Tunis.
But Mr. Hinton has been good enough to examine for me the copy in the
British Museum of Schloezer's Briefwechsel, 1776, on p. 339 of which Rothmann
described Mus gundi. The result is very unexpected, for that work shows that
Rothmann was not in the Great Atlas at all, but made his journey inland
from the town of Tripoli, and obtained his Gundi in the hills of Gharian (spelt
Garean by him), some 80 kilometres south of that place. Masuffin was a
little farther on, and was mentioned, but was not the place where the Gundi
was found.
Now the expression " testaceo rufescens " used by Rothmann in his diagnosis
suits exceedingly well the strong-coloured Gundis from South Tunis sent by
M. Blanc, and the relation of the localities to each other is such that it is quite
natural that the same form should occur in both. I should therefore propose
to identify the Tunisian specimens as representing the true Gundi of Rothmann.
In the Proceedings of the Zoological Society jor 1830, p. 48, an account was
given by Mr. Yarrell of two Gundis which had been sent by Colonel Hanmer
Warrington from Tripoli, and of these, one — B.M. No. 55.12.24.128,
Zoological Society's MS. list, No. 311 — is still in the Museum. Pending the
arrival of specimens from Gharian, this latter may be taken as a topotype
of C. gundi.
The importance of this Tripoli specimen lies in the fact that one bulla is
still extant in the skull, and is of the small size characteristic of the ordinary
Algerian Gundi, with no resemblance to that of the Middle Tripolitan C. vali,
Thos. Presumably, therefore, Rothmann's Gundi was not the latter species.
But since the name gundi now proves to belong to the vivid-coloured eastern
form, the question naturally arises as to the proper name of the Biskra Gundi,
which as already indicated, may be subspecifically distinguished from true
gundi by its duller and more drab coloration.
On examination I find that the two cotypes of Gray's Ctenodaclylus massoni
are absolutely and exactly like ordinary Biskra Gundis, and might very well have
come from there. In consequence, I propose to term that animal C. gundi
massoni, and to take Biskra as representing the typical locality of the subspecies.
NOVITATES ZOOLOGICAE XXVII. 1920. 507
Of this most interesting group we have therefore, proceeding from east
to west, the following six recognisable forms :
1. Ctenodactyhia vali Thos., Middle Tripoli.
2. Ctenodaclylus gundi gundi Rothmann, N.W. Tripoli and S. Tunis.
3. Ctenodactylus gundi massoni Gray, southern slopes of Algerian Atlas,
Biskra.
4. Massoutiera mzabi Lat., Mzab, Algerian Sahara.
5. Massoutiera harterli Thos., Southern Algerian Sahara.
6. Felovia vae Lat., Felou, Senegal.
508 NOVITATES ZOOLOQICAE XXVII. 1920.
SUPPLEMENTARY NOTES ON DIOPTIDAE.
By LOUIS B. PROUT, F.E.S.
ALTHOUGH — as anticipated — I have not been able to follow up the study
of this interesting family since publishing my " Provisional Arrangement "
(Novitates Zoologicae, XXV. 395-429), I have come across a few additions
and corrections to which it seems a duty to call attention. I may also take
this opportunity to point out that Monsieur Dognin, in his valuable work,
Hitiroceres Nouveaux de V Amirique du Sud, fascicule xv. pp. 7-8 (February 1919),
has published the following synonymic and taxonomic notes :
Phaeochlaena costidentata Dogn. is certainly the $ of bicolor Mosch. (as I
suggested with ?).
Myonia conjuncta Dogn. is the same species as cilrina Druce.
Momonipta pellucida Dogn. (Scotura), Hit. Nouv. Amir. Sud, i. 16 (1910),
omitted in my list, is near jipiro Dogn., agreeing in markings but smaller and
much more contrasted. From Colombia.
Tanaostyla disconnexa Dogn., Hit. Nouv. Amir. Sud, iii. 21 (relegated by
me to the species incertae sedis), is really referable to this genus. (M. Dognin,
in litt. January 12, 1919, wrote me that it " was placed in this genus by Warren,
and, I think, with reason. It fits . . . fairly exactly, except that cell of forewing
is less than two-thirds — about one-half, 7, 8, 9, 10 stalked from upper angle of
cell, DC of hind wing oblique but straight at two-thirds of wing.")
Phaeochlaena augustimacula Dogn., Ann. Soc. Ent. Belg., xlvi. 475, is a
Tithraustes near albitumida Dogn.
Two new Myonia forms have since been published by the same author :
12a. biplagiata peruviana Dogn., Hit. Nouv. xvii. 11 (1919) (Peru).
13 bis. primula Dogn., Hit. Nouv. xvii. 10 (1919) (graba form. ?) (Ecuador).
On account of Druce's deplorable ignorance of systematic entomology, I
overlooked three of his types which should have been studied in connection
with my work, but which have only just been unearthed in my preparations
for arranging Mr. Joicey's Larentiinae, they having been described under
Trochiodes (!). These are the following :
Trochiodes coniades Druce, Proc. Zool. Soc. Lond. 1893, p. 309, t. xxi. f. 21.
An aberrant Tithraustes (?), possibly akin to mirma Druce, but the $ antenna
simple. A (J in coll. Brit. Mus. has lost both antennae.
Trochiodes (?) coras Druce, Proc. Zool. Soc. Lond. 1893, p. 310. A Momonipta,
supplanting biplaga Dogn. I have only previously seen the colour-form (?)
flaviplaga Dogn. The actual status of the two forms can hardly be decided
without ampler material.
Trochiodes plataea Druce, Proc. Zool. Soc. Lond. 1893, p. 310, t. xxi. f. 22.
A Xenorma, very distinct from anything yet known to me. Druce's 11 are all
In the genus Myonia is to be placed :
36. maera Schaus, inadvertently cited by me on p. 422 as Josia, No. 18,
but really a near ally of evippe Walk.
NOVITATES ZOOLOGICAE XXVII. 1920. 509
On p. 404, under Tolimicola, read :
1. consanguinea Dogn., Hit. Nouv. hi. 22 (1911) (Tithraustes) = jassli Prout
(from correspondence with its author I have no doubt that consanguinea is
the $ to my jassli. The " second species, too worn to describe," is perhaps
nubilata Dogn., which I cited on p. 410 as a doubtful Tithraustes).
Under Xenorma :
X. ovata Dogn. is to be accorded specific rank, its palpus and tegulae being
black, not yellow as in cytheris.
Under Oricia :
O. damalis Schaus is, I now feel convinced, the <J of homalochroa.
Under Tithraustes :
Dognin, in litt., suggests that pyrijera Dogn. (No. 14) may well be merely a
local variation of caliginosa Dogn. (No. 15).
16. inaequiplaga Dogn. I now gather that this is very close to tiznon Dogn.
(listed by me as Polypoetes, No. 3), whence it is clear that one or other of these
species is at present wrongly placed.
Under Josia :
3. abrupta ab. icca is a curiosity of nomenclature. I find the name given
" without elucidation " was by Butler, and was a misreading of a scribbled
" Scea " appended to one of the specimens by Walker (!). It is, moreover, not
exclusively a $ aberration, one of the British Museum examples being a (J.
47 bis. andosa Druce, Ann. Mag. Nat. Hist. (8) vii. 290 (1911) (Josiomorpha)
(Colombia) is to be intercalated.
58. latifascia Prout, nom. nov., is to be substituted for lativitta Warr. (nee
Walk.). Mr. Tarns has called my attention to the fact that a nom. bis ledum
stands in the genus as at present constituted.
Under Scea :
8. gigantea gigantea Druce, Ann. Mag. Nat. Hist. (6) xviii. 42 (1896)
(Thirmida) (Bolivia), = caesiopicta Warr., Nov. Zool. vii. 128 (1900) (Bolivia).
8a. gigantea cyanea Prout, Nov. Zool. xxv. 425 (1918) (S.E. Peru).
Under the species incertae sedis (p. 429) :
Ephialtias superbior Strand is an Amatid = Ctenncha cyaniris Hmpsn. $.
Josia gigantea Druce is probably an Aganaid (sens, lat.), as M. Dognin tells
me that his Josiomorpha flammata (Ann. Soc. Ent. Belg. liii. 223) is evidently
very close to it, if not even a race, and certainly belongs to that family (= Calli-
morphidae Hmpsn., Hypsidae Hmpsn. olim).
33
510 Novitates Zoological XXVII. 1920.
ON SOME AFRICAN SPHINGIDAE.
By DR. KARL JORDAN.
(With five text-figures.)
Litosphingia gen. nov.
<J. Generibus Hoplistopas et Praedora dictis similis, sed tibia antica duabus
spinis lateralibus arniata et intermedia haud spinosa distinguenda.
Tongue well developed ; genal process large ; pilifer with bristles only.
Antenna not distinctly club-shaped, cilia as in Hoplistopus. Palpus just visible
from above, joint between segments I and II slightly open. Head with a feeble
median crest. Foretibia with two spines, both lateral ; foretarsal segment I
one-third shorter than foretibia, likewise with two lateral spines, the first sub-
median, the second apical, segments II to V together very little longer than
tibia. Midtibia without spines, without comb. Hindtibial apical inner spur
about one-third the length of the first hindtarsal segment. Pulvillus present ;
paronychium with one lobe each side. Spines on abdominal tergites very weak.
Genitalia : Tenth tergite compressed, its apex widened, rounded in dorsal
view, convex above and concave beneath. Tenth sternite much shorter than
tergite, pointed. Clasper without friction-scales, short. Penis-sheath with a
peculiar rim around apex.
Neuration : Lower cell-angle of fore wing obtuse ; SC2 and R1 of hind wing
on a very short stalk, cross-vein D2 incurved, nearly double as long as D5.
$ and early stages not known.
One species.
1. Litosphingia corticea spec. nov.
cJ. Grisea ; abdomine linea mediana dorsali continua nigra bene expressa
notato. Ala antica elongata angulo postico valde obtuso subrotundato, grisea
nigro suffusa, basi macula longitudinali diffusa mediana griseo-alba, venis plus
minusve nigris in area submarginali griseo-albo striatis, fascia sat lata nigra e
duabus maculis inter apicem et venam R1 sitis composita in discum continuata,
ubi reducta diffusa inconspicua. Ala postica grisea nigro-venata. Cilia nigro-
guttata.
Al. ant. long. 24 mm., lat. 8'5 mm.
Hab. Umvuma, S. Rhodesia, 1 8. i. 1918 (A. A. Carnegie) ; one <J in Rhodesia
Museum.
Head, pronotum, and the middle of the meso-metanota suffused with
black, the patagia whitish grey ; black median line of abdomen continuous,
almost one millimetre broad anterior^, narrowing backwards ; no lateral spots.
Hind angle of forewing much more rounded than in the species of Praedora
and Hoplistopus, but less so than in Ellenbeckia. The pale upper scales on both
wings bidentate, the long ones of upper side narrowing apically, many truncate,
Novitates Zooloqicae XXVII. 1920.
511
the large underscales tridentate, but the middle tooth often missing ; few under-
scales in cell of forewing beneath.
Grey, suffused with black. Forewing : a whitish grey streak from base
to M2 below cell, posteriorly bordered by a black line which is slightly longer,
a median line in cell and the veins black, on disc between R3 and M2 two black
streaks ; from apex to R1 two black spots sharply defined costally, more diffuse
distally, forming a short oblique band which is continued by a faint diffuse
cloud, between R1 and R2 a blackish line from near cell to near fringe, in sub-
marginal area the veins each with a more or less distinct whitish-grey dash ;
fringe with blackish dots at ends of veins. Hindwing almost uniformly blackish
grey, the veins black, thin, abdominal area paler.
Underside without markings excepting the fringe-spots, which are more
clearly defined than above.
Genitalia (text-figs. 1-5) : Tenth tergite (x.t.) entire, the apical process
in dorsal aspect spoon-shaped, being proximally compressed and apically rounded-
dilated ; in a lateral view the process is highest in its proximal half, the apical
half being depressed and gently curved downwards ; underside of apical dilata-
tion concave. Tenth sternite (x.st.), in a ventral view, with the sides parallel
to about two-thirds, apical third narrowing to a point, the apex being curved
upwards. Clasper (text-fig. 4) irregular in shape, dorsal margin convex, apex
produced as a lobe, below which the margin is incurved ; outer surface divided
by a longitudinal groove ; dorsal margin armed with numerous small teeth
directed proximad. No friction-scales. On the inner side the dorsal margin
proximally dilated into a large lobe, bent down and covering part of the cavity
of the clasper ; this lobe dentate. Harpe divided by a deep longitudinal groove
into a broad convex ventral ridge and a thin sharp dorsal one, each ending
distally with a recurved conical tooth, the two teeth lying one behind the other,
the distal one, which belongs to the ventral ridge, being the longer of the two ;
from the wide proximal portion of the harpe an intermediate, shortened ridge
extends into the groove of the harpe ; above the harpe and partly covered
by the dorsal marginal lobe a small double ridge. Penis-sheath (text-fig. 5)
512 NOYITATES ZOOLOQICAE XXVII. 1920.
terminating with a collar of which the proximal edge is detached from the
sheath, the distal edge forming a triangle of which the ventral corner projects
most ; this collar in a lateral view somewhat resembles the flat-crowned three-
cornered hat of our forefathers.
2. Xenosphingia jansei Jord. (1920).
Described from a single $ on p. 169 of the present volume. Mr. A. T. Janse
has now kindly sent us, for the Tring Museum, a ? of this interesting species.
This sex differs from the $ especially in the palpus, of which the third segment
is long and rod-like as in <J, but porrect and not curved sideways. The pec-
tination of the antenna is not quite so long as in J. The neuration differs in
SC! of forewing being nearer to apex of cell than to SC1, and in D2 of hindwing *
being but slightly longer than DJ.
The $ was obtained by Mr. Janse at Sawmills, South Rhodesia, in January
1920.
3. Temnora cinereofusca Strand (1912).
In Nov. Zool. xxiii. p. 118, No. 6 (1916) we said that we regarded cinereo-
fusca as synonymous with T. reutlingeri. I have lately seen in the Berlin
Museum a specimen of true cinereofusca. The species is not T. reutlingeri, but
comes close to T. subapicalis R. & J. (1905), from which it differs in the more
greyish coloration.
4. Nephele rosae illustris subspec. nov.
Nephele rosae, R. & J, Revis. Sphing.,-p. 563, no. 486(1903) (pt. ; Nguelo).
$. Fascia alba alarum anticarum lata a costa usque ad marginem posticum.
Hab. Inyamadzi, Portug. East Africa, 2,000 ft., 28. v. 1916 (Swinnerton),
1 $ in coll. Janse, type ; Nguelo, German East Africa, 1 $, and Pemba Island
(E. Morland), 1 $, in the Tring Museum.
On an average larger than the West African subspecies. The white band
of the forewing broader, of almost even width from costa to hindmargin ; the
pale line placed outside this band more or less scaled white towards costa.
Our two specimens are rather poor, while the one in coll. Janse is very fine,
having been bred from the chrysalis.
In the West African race, N. r. rosae, the white band of the forewing varies
very much in width, being sometimes almost a mere line, sometimes posteriorly
several millimetres wide, but is always narrower towards the costal margin
than at the hindmargin. The stigma of the forewing is usually present in N. r.
rosae ; in the above three specimens of N. r. illustris it is absent.
* In the description of Xenosphingia read D2 instead of D*.
A List of the Contents of the first 25 volumes of Novitates Zoologicae, 1894-1918,
arranged according to Subjects and Authors, is in course of preparation and will
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A REVISION OF THE LEPI DOPTEROUS FAMILY
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By the Hon. WALTER ROTHSCHILD, Ph.D.,
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NOYITATES ZOOLOGICAE
H Journal of Zoology
V
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EDITED BY
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Dr. ERNST HARTERT. and Dr. K. JORDAN.
Vol.
XXVII.
3'h mas^
No. 3.
Pages 513—544.
Plates
XIV— XVII.
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18th, 1921
at the Zoological Museum, Tring.
PRINTED BY HAZELL, WATSON k VLNEY, Ld„ LONDON AND AYLESBURY.
1921.
Vol. XXVII.
NOVITATES Z00L0GICAE.
EDITED BT
LOED ROTHSCHILD, ERNST HARTERT, and KARL JORDAN.
CONTENTS OF NO. III.
PAGES
INDEX TO VOLUME XXVH 513—544
(TITLE-PAGE, CONTENTS, LIST OF PLATES TO VOLUME XXVII.)
INDEX.
Abbotornis 454.
abdallah (Agrotis), 30.
— (Euxoa), 30.
Abrornia, 502.
Abrostola, 115.
abyssinia (Spodoptera), 15.
abyssinjea (Coracias), 330.
— (Zosterops), 432.
abyssinicus (Coracias), 330.
abyssinus (Coracias), 330.
Acanthiza, 461.
Aeanthopneuste, 461, 462.
accentifera (Phytometra), 87.
— (Plusia), 87.
Accentor, 503.
accentor (Androphilus), 485.
Acidalia, 298.
Accipiter, 205.
accipitrina (Eumichtls), 60.
— (Phalaena), 60.
accipitrinus (Asio), 150.
achemenides (Oryba), 347, 390.
Acontia, 75.
Acrobyla, 98.
Acrocephalus, 153, 189, 190, 464.
Acronycta, 7.
acrosticta (Oortyta), 93.
— (Pericyma), 93.
Actinotia, 8.
acuminata (Erolia), 137.
acuta (Anas), 142, 214.
— (Chaetura), 330.
— (Hirundo), 330.
acutipennis (Capriraulgus). 330.
— (Chordeiles), 330.
adamantina (Omphalophana), 70.
adarasi (Mimus), 478.
— (Nesomimus), 478.
adamsii (Colymbus), 129.
addita (Microeca), 490.
admiralitatis (Zosterops), 435.
adulatriz (Noctua), 87.
— (Phlogophora), 87.
Aegithalos, 185, 441, 442.
Aegle, 73.
Aegolius, 150.
35
aegra (Oenanthe), 470.
aeruginosus (Circus), 204.
aerumna (Bryophila), 2.
Aesalon, 149.
aesalon (Falco), 202.
Aethia, 131.
aethiopica (Platysteira), 496.
Aetbopyga, 425.
aeton (Bryophila), 3.
afer (Nilaus), 449.
affinis (Arckanara), 14.
— (Cardepia), 57.
— (Cleophana), 68.
— (Derthisa), 21.
— (Ianthocincla), 488.
— (Lams), 246.
— (Nesomimus), 478.
— (Nyroca), 143.
— (Prinia), 457.
— (Trochalopteron), 488.
aflouensis (Sidemia), 45.
afra (Cinnyris), 425.
africana (Alauda), 329.
— (Certhilauda), 329.
— (Hecatera), 48.
— (Hylophila), 115.
— (Oria), 14.
— (Tapinostola), 14.
Aganistlios, 343.
Aglossestra, 21.
Agriopis, 55.
Agrophila, 74, 77.
agrotina (Actinotia), 8.
— (Lycophotia), 8.
Agrotis, 8, 16, 24-34, 111.
audacis (Muscieapula), 492.
aignani (Zosterops), 436.
Aix, 214.
alani (Zosterops), 435.
Alauda, 151, 182, 329.
alba (Crocethia), 138.
— (Motacilla), 152, 153, 183, 184.
— (Procnias), 330.
— (Tyto), 200.
albatrus (Diomedea), 135.
albellus (Mergus), 147, 221.
513
514
albeola (Bucephala), 145.
alberti (Pachycephala), 446.
— (Zosterops), 437.
albescens (Pristorharnphus), 431.
albicans (Anthophila), 81.
— (Eublemma), 81.
albicapilla (Cossypba), 473.
albiceps (Mecocerus), 260.
albicilla (Haliaetus). 150, 206.
— (Muscicapa), 153.
— (Sipbia), 153.
albida (Antbophila), 81.
— (Eublemma), 81."
— (Timora), 13.
atbidior (Eublemma), 84.
albifrons (Anser), 141, 210.
— (Pentholaea), 472.
— (Sterna), 244.
albigularis (Poecilodryas), 495.
■ — (Smithornis), 496.
— (Tregellasia), 495.
albimacula (Bryopbila), 4.
albina (Rhipidura), 498.
albipectus (Thryothorus), 505.
albiplaga (Protoparce), 347, 3US.
albipuncta (Noctua), 9.
— (Sideridis), 9.
albistriatus (Oriolus), 331.
albivestalis (Eublemma), 84.
albolineata (Brachygalea), 64.
— (Colopbasia), 64.
albomaculata (Biyophila), 4.
albonotata (Poecilodryas), 495.
— (Pratincola), 471.
— (Saxicola), 471.
albovenosana (Earias), 115.
album (Cirpbis), 11.
— (Phalaena), 11.
Aleatras, 332.
Alcedo, 197, 330.
alchymista (Catephia), 94.
— (Mageutica), 94.
— (Phalaena), 94.
Alcippe, 481.
Alectoris, 251.
Aleuron, 396, 397.
aleutica (Sterna), 132.
alexandrinus (Charadrius), 136, 234.
alfredi (Bradypterus), 468.
alfurorum (Pachycephala), 449.
algae (Bryophila), 4.
— (Noctua), 4.
algira (Emmelia), 74.
— (Paralalia), 107.
— (Phalaena), 107.
algiriae (Cerocala), 10S.
algirica (Cirpbis). 10.
— (Cirrhoedia), 41.
algirica (Cymatuphora), 41.
— (Enargia), 41.
— (Leucania), 10.
— (Stilbia), 14.
— (Triphaena), 35.
alifura (Dendrobiastes), 493.
— (Museicapula), 493.
alifurus (Dendrobiastes), 493.
alinae (Cinnyris), 426.
alisteri (Cinclosoma), 488.
Allamanda, 349.
allamandae (Isognathus), 343, 349, 381.
alle (Plotus), 247.
allochroma (Chlorissa), 266.
Allocotops, 487.
alma (Scopula), 307.
almoravida (Calophasia), 71.
alope (Erinnyis), 384.
alpigena (Eremobia), 59.
— (Hadena), 59.
alpina (Erolia), 138, 236.
Alseonax, 489.
alsines (Athetis), 16.
— (Noctua), 16.
altirostris (Argya), 486.
— (Crateropus), 486.
aluco (Strix), 200.
amabilis (Malurus), 457.
amadis (Xylophanes), 411.
Amathes, 637-9.
ambigua (Athetis), 17.
— (Noctua), 17.
— (Stachyridopsis), 480.
Amephana, 65, 66, 69.
americana (Nyroca), 143.
— (Oidemia), 147.
Ammetopa, 49, 50.
Ampelis, 329.
Amphimoea, 363.
Amphipyra, 89, 90.
Amplypterus, 372.
Amytornis, 456.
anaemica (Bryophila), 5.
Anas, 212, 213, 214, 332.
anatoliae (Parus), 442.
anatreces (Scopula), 287.
anehemolus (Pholus), 347, 403.
androgeus (Papilio), 343.
Androphilus, 485.
angelus (Taterillus), 317.
anglicus (Dryobates), 197.
anglorum (Regulus), 185, 441.
angolensis (Arachnothera), 428.
angularis (Bombycia), 112.
— (Calophasia), 1 12.
angusticauda (Cisticola), 467.
angusticincta (Bytharia), 306.
Anisodes, 271-9, 301-6.
515
Anomala (Stilbia), 14.
Anser, 141, 142, 143, 210, 211.
anser (Anser), 210.
ansorgei (Alseonax), 489.
— (Anthoscopus), 441.
— (Apalis), 461.
— (Calamocichla), 464.
— (Cinnyris), 425.
— (Cisticola), 466.
— (Diapborophyia). 495.
— (Harpoleatea), 450.
— (Muscicapa), 489.
— (Parmoptila), 432.
— (Sylvietta), 460.
— (Xenocopsychua), 473.
antaeus (Coeytius), 362.
Antarchaea, 109.
Anthoecia, 73.
Anthophila, 78, 81, 85.
Anthoscopus, 441, 442.
Anthracia, 92.
Antkreptes, 428, 429.
Anthus, 151, 152, 182.
antias (Bryophila), 5.
antillarum (Mimus), 477.
antinorii (Lanius), 452.
antiquus (Synthliborhamphua), 131.
Antitype, 51-3.
antitypina (Miselia), 48.
— (Polia), 48.
Anua, 105.
anubus (Xylophanes), 349, 410.
Anumeta, 95-7.
Anydrophila, 97.
anysa (Pandesma), 93.
Apalis, 460, 461.
Apamea, 43, 44.
Apivorus (Pernis), 206.
apo (Dicaeum), 429.
apolia (Cinnyris), 428.
Apopeates, 90, 91.
Aporphyla, 54.
approximans (Athetis), 18.
apricarius (Charadriua), 234.
aprilina (Agriopia), 55.
Apus, 196.
apus (Apua), 196.
aquatieus (Rallus), 249.
Aquila, 202.
arabica (Cisticola), 465.
arabs (Hadena), 59.
— (Parastichtia), 59.
araburn (Saragosaa), 43.
Aracbnotbera, 427, 428.
arada (Leueolepis), 329.
— (Myrmornis), 329.
arborea (Lullula), 182.
Arcbanara, 14.
aretica (Fratercula), 248.
— (Sterna), 131.
arctieus (Colymbua), 130, 230.
Ardea, 140, 208.
Arenaria, 136.
arenaria (Calidris), 138.
arenosa (Clytie), 106.
Arenostola, 14.
areola (Dicbonia), 60.
arfakiana (Sericornia), 461.
argentatus (Larus), 132, 245.
argentina (Empusada), 63.
— (Xoctua), 63.
argentosa (Aniaodea), 278.
— (Perixera), 278.
argillaceago (Antitype), 52.
argutus (Proparua), 481.
Argya, 486.
argyritia (Leucania), 9.
— (Sideridia), 9.
Argyroapila, 8, 13.
arida (Eublemma), 83.
arimanon (Psittacus), 331.
Armada, 76, 98.
arquata (Numenius), 241.
arra (Uria), 130.
Arremon, 328.
Artamua, 455.
Artaxa, 321.
artburi (Pachycephala), 448.
arundinaceus (Acrocephalua), 464.
arvensis (Alauda), 151, 182.
Arvicanthis, 319.
Asio, 150, 199, 200.
asperaa (Athetia), 16.
— (Caradrina), 16.
aaaamensis (Ianthocinola), 488.
astigmata (Atbetia), 17.
ater (Parua), 184, 444.
Athene, 199.
Athetis, 15-19, 111, 112.
atra (Fulica), 250.
— (Rhipidura), 498.
atricapilla (Sylvia), 190.
atricapilla (Zoateropa), 435.
atricapillus (Parus), 158, 185, 443.
atrieollis (Eremomela), 461.
atrosignata (Anumeta), 95.
atthis (Alcedo), 197.
audacis (Dendrobiastes), 492.
— (Geocichla), 476.
— (Turdus), 476.
auguroide8 (Agrotis), 36.
augustimacula (Phaeochlaena), 508.
aurantiacus (Antarchaea), 109.
aurantiifrons (Hylophilua), 450.
— (Pachysylvia), 456.
aureola (Emberiza), 155.
516
aurifera (Noctua), 87.
aurimacula (Turdus), 476.
aurita (Amephana), 69.
— (Noctua), 69.
auritus (Podiceps), 129, 225.
austauti (Cosniia), 40.
— (Xanthia), 40.
australe (Dicaeum), 328.
australis (Epistor), 399.
— (Harpolestes), 450.
— (Metoptria), 86.
— (Pipra), 328.
— (Synthyrnia), 86.
— (Telophonus), 450.
Autophila, 91, 92.
autumna (Simyra), 8.
averano (Ainpelis), 329.
— (Procnias), 329.
axillaris (Pratincola), 472.
— (Saxicola), 472.
Axylia, 61.
Azenia, 86.
azorensis (Cosymbia), 271.
azurea (Callisitta), 440.
— (Hypothymis), 496.
baeri (Nyroca), 216.
baiidi (Burnesia), 457.
— (Prima), 457. .
bakeri (Ianthocincla), 487.
— (Trochalopteron), 487.
balestrei (Catamecia), 65.
baliensis (Cyanoderma), 480.
— (Rhinomyias), 499.
balnearia (Polydesma), 93.
balteatus (Mecocerus), 260.
bambusicola (Turdus), 476.
banyumas (Cyornis), 491, 492.
bassana (Sula), 222.
Batbmocercus, 483.
batjanensis (Phyllergates), 468.
baucis (Pentholaea), 472.
baueri (Limosa), 138.
bauri (Minius), 478.
— (Nesomimus), 478.
beata (Cucullia), 62.
beelzebuth (Cocytius), 362.
benenotata (Hypoglaucitis), 94.
bengalensis (Houbaropsis), 331.
— (Otis), 331.
benguellensis (Erytbropygia), 472.
bernicla (Branta), 142, 211.
Bessonornis, 470.
bewickii (Cygnus), 210.
biarmicus (Panurus), 186.
bicolor (Elacbyophtbalma), 324.
— (Erythrooichla), 482.
bicolor (Prionochilus), 430.
— (Proxemus), 112.
bicruris (Miselia), 47.
— (Phalaena), 47.
bidentatus (Bucco), 328.
bilineata (Bryopbila), 4.
bilkevitchi (Cinclus), 504.
bindloei (Mimus), 478.
— (Nesomimus), 478.
bineschensis (Cinnyris), 426.
biskrae (Hadena), 59.
— (Parastichtis), 59.
biskrana (Cucullia), 62.
biskrensis (Acontia), 75.
— (Cerocala), 108.
— (Tarache), 75.
blakistoni (Alauda), 151.
blanda (Atbetis), 16.
— (Noctua), 16.
blandula (Eublemma), 85.
— (Noctua), 85.
blanfordi (Cisticola), 466.
— (Parisoma), 495.
blasii (Hypothymis), 496.
blatteriae (Cucullia), 62.
— (Phalaena), 62.
bledi (Agrotis), 24.
bocagei (Turdus), 476.
boetica (Cleophana), 66.
boisdefirei (Grammodes), 107.
— (Ophiusa), 107.
Bombycia, 54, 112.
Bombycilla, 153, 187.
Bombyx, 21, 32, 54, 55.
bonga (Dicaeum), 430.
bontbaina (Cyornis), 492.
— (Siphia), 492.
borealis (Phylloscopus). 154, 463.
borin (Sylvia), 190.
bomeensifl (Enicurus). 474.
— (Henicurus), 474.
— (Myiophoneus), 479.
— (Stachyris), 4S1.
— (Tchitrea), 499.
Borolia, 116.
boschas (Anas), 142.
Botaurus, 209.
bourkei (Platysphinx), 165.
bouveti (Agriops), 55.
brachydactyla (Certhia), 438, 439.
Brachycola, 302, 303.
Brachygalea, 64.
brachypterus (Bradypterus), 469.
Brachypteryx, 479.
Urachyrhamphus, 130.
hrachyrhynchus (Laius), 133.
brachyura (Muscicapa), 329.
(Myrmotherula), 329.
517
brachyura (Sylvietta), 460.
Bradyornis, 489.
Bradypterus, 468, 469.
branickii (Odontorhynchus), 505.
Branta, 141, 142, 211.
Brassolis, 343.
brevicauda (Urallaria), 329.
— (Forrnicarius), 329.
brevicaudata (Camaroptera), 459.
brevipennis (Rheotes), 453.
brevipes (Tringa), 139.
brevirostris (Rissa), 134.
britannica (Carduelis), 176.
— (Certhia), 184.
— (Sitta), 184, 439.
britannicus (Cinclus), 195.
— (Lyrurus), 250.
— (Parus), 184.
Brithys, 15.
brodiei (Monarcha), 503.
brunnea (Colluricincla), 453.
— (Proparus), 481.
brunneiceps (Brackypteryx), 479.
brunneus (Proparus), 481.
Bryomima, 00.
Bryophila, 2-5, 15, 46, 76, 111.
bryophiloides (Catamecia), 3.
bubastus (Madoryx), 395.
Bucco, 328.
Buoephala, 144, 145, 218, 332.
buchanani (Desmodilliscua), 317.
budongoensis (Cryptolopha), 502.
bugeaudi (Agrotis), 30.
— (Euxoa), 30.
bulunensis (Hylopbilus), 456.
bungurense (Malacopterum), 482.
bungurensis (Setaria), 482.
Burbinus, 233.
burkii (Cryptolopba), 501.
Burnesia, 457.
buruensis (Cinnyris), 427.
— (Erythromyias), 493.
— (Myiagra), 500.
— (Pacbycepbala), 448.
Butalis, 153.
Buteo, 149, 203.
buteo (Buteo), 203.
butleri (Cryptolopha), 501.
— (Madoryx), 395.
biittikoferi (Cinnyris), 427.
buxtoni (Lithoslege), 312.
Bytharia, 306.
cabaret (Carduelis), 178.
cabrerae (Turdus), 477.
caerulescens (Anser), 141.
caeruleus (Parus), 184, 442.
caesiopicta (Thirmida), 509.
caffer (Hipposideros), 315.
cagayanensis (Mixornis), 480.
caicus (Grammodia), 386.
caid (Anthophila), 82.
cailino (Heliothis), 98.
— (Syneda), 98.
calabra (Rhodostrophia), 268.
calama (Anisodes), 274.
— (Pisoraea), 274.
Calamia, 14.
calamistis (Sesamia), 13.
Calamocicbla, 464.
Calamoherpe, 464.
Calamonastes, 465.
calandra (Emberiza), 180.
calberlae (Caradrina), 14.
— (Stilbia), 14.
Calcarius, 155.
calendulae (Cucullia), 63,
Calidris, 138.
calidus (Falco), 149.
caliginosa (Hydrilla), 110.
— (Miselia), 110.
— (Noctua), 110.
Callaeops, 498.
Calliope. 474.
calliope (Luscinia), 154.
Callisitta, 440.
Calophasia, 54, 70, 71, 112.
calvus (Allocotops), 487.
Camaroptera, 459.
caraburni (Tchitrea), 499.
campanisona (Myrmorius), 329.
— (Myrmothera), 329.
campbelli (Scopula), 296.
canadensis (Ardea), 140.
— (Branta), 141, 142.
— (Megalornis), 140.
canagicus (Anaer), 142.
candicans (Falco), 148.
candidana (Eublemma), 86.
— (Pyralis), 86.
canicapilla (Jlalacocincla), 484.
canicapillus (Turdinus), 484.
caniceps (Sigmodus), 452.
cannabina (Carduelis), 178.
canorura (Ianthocincla), 487.
— (Trocbalopteron), 487.
canorus (Cuculus), 150, 198.
canroberti (Erithrophaia), 73.
canteneri (Metopoceras), 49.
— (Polia), 49.
canus (Lams), 133, 245.
canutus (Erolia), 235.
caparo (Turdus), 475.
capensis (Certhilauda), 329.
— (Smithornis), 496.
51*
cappa (Miaelia), 116.
— (Noctua), 116.
caprata (Pratincola). 471.
— (Saxicola), 471.
Caprimulgua, 196, 330.
capronnieri (Pholua), 400.
capsenaia (Euxoa), 24.
Garadrina, 14, 16, 17-19. 1 12.
carbo (Phalacroeorax), 221.
Cardepia, 57, 58.
Carduelis, 156, 176, 177, 178.
carduelis (Carduelis), 176.
caricae (Isognathus), 377.
carinata (Aleuron), 396.
caroli (Anthoscopua), 441.
Carpodacus, 157.
carpophaga (Miselia), 46.
— (Phalaena), 46.
carringtoni (Mimua), 478.
— (Nesomimus), 478.
caryocatactea (Nucifraga), 174.
Casarca, 212.
caachmirenaia (Parus), 44:1.
casearia (Athetia), 16.
— (Caradrina), 16.
caataneiceps (Cryptoloplia), 501.
caataneiventria (Monarchal, 503.
castaneua (Androphilua), 485.
— (Turdinus), 485.
caatanonotus (Eupetea), 488.
Catablemma, 77, 83.
Catamecia, 3, 6, 65.
cataphanea (Spintheropa), 91.
Cataponera, 487.
Catephia, 94, 95, 96.
cathartica (Allamanda), 349.
Catooala, 98, 99-104.
caudatua (Aegithaloa), 185, 442.
— (Crateropus), 486.
— (Paeudotharrhaleua), 484.
caurensis (Thryothorua). 505.
cavifer (Epi8tor), 399.
ceculua (Seaia), 401.
celaenopa (Merula), 476.
— (Turdue), 476.
Celerio, 338.
celsicola (Agrotia), 32.
— (Euxoa), 32.
centralia (Bradypterua), 469.
Centropodia, 51.
Ceroomela, 471.
cerealia (Autophila), 92.
Cerocala, 108, 109.
cerris (EurnichtiB), 60.
— (Hadena), 60.
Certhia, 184, 438, 439.
Certhilauda, 329.
perviniventria (Eumyiaa), 491.
cerviniventria (Stoparola), 491.
cervinua (Anthua), 151.
ceatis (Anumcta), 96.
— (Catephia), 96.
Cettia, 458.
ceylonenaia (Culicicapa), 500.
chabordis (Cleophana), 68.
Chaetura, 330.
chalcytea (Noctua), 87.
— (Phytometra), 87.
chalybeocephalua (Monarchal , 602.
chamomillae (Cucullia), 63.
chanzyi (Anthoecia), 73.
— (Heliothis), 73.
Charadriua, 136, 234.
Chariclea, 72.
chenopodiphaga (Mameatra), 42.
— (Paeudohadena), 42.
Chesiaa, 76.
chimaera (Namaugana), 45.
— (Scotogramma), 57.
chinenaia (Streptopelia), 232.
chioleuca (Aporphyla), 54.
— (Polia). 54.
chiron (Xylophanea), 349, 412.
Chloridea, 72, 73.
chlorion (Eariaa), 115.
Chloris, 176.
chloria (Chloris), 176.
— (Zoateropa), 434.
Chloriasa, 266.
Chlorocharia, 437.
chloronota (Sylvictta), 460.
chloronotus (Orthotouiua), 468.
Chloropeta, 495.
Chlorophoneus, 451.
chlorophyllana (Eariaa), 115.
chloroptera (Aleuron), 396.
chloropus (Gallinula), 249.
chloropygia (Cinnyris), 426.
chocolatinus (Dioptrornis), 489.
— (Muscicapa), 489.
ChordeUea, 330.
chretieni (Borabycia), 54.
— (Calophaaia), 54.
chriatinae (Aethopyga), 425.
chriatophi (Agrotia), 30.
— (Euxoa), 30.
chrysaetus (Aquila), 202.
chryaitis (Phytometra), 115.
Ciconia, 207.
ciconia (Ciconia). 207.
Cimelia, 89.
Cincloaoma, 488.
Cinclus, 195, 504.
cinclua (Cinclus), 195, 504.
cineraacena (Monarchal, 502.
— (Parua), 442.
519
cinerea (Ardea), 208.
— (Motacilla), 152, 183.
— (Setaria), 482.
cinereiceps (Eopsaltria), 444.
— (Hemichelidon), 489.
— (Poecilodryas), 444.
cinereicollis (Phyllergates), 467.
cinereofusca (Temnora), 512.
cinereum (Malacopterum), 482.
cinereus (Artamus), 455.
cingulata (Herse), 334, 347, 361.
cinnamomeogrisea (Polia), 43.
cinnamonieus (Bradypterus), 469.
— (Hypocryptadius), 438.
cinnamomina (Catamecia), 6.
■ — (Scotogramma), 56.
Cinnyris, 425-7, 428.
cinochrea (Dianthocia), 111.
— (Epia), 111.
cirlus (Emberiza), 181.
Circus, 204.
Cirphis, 9-12. 115.
cirrhata (Lunda), 131.
Cirrhoedia, 41.
Cisticola, 465-7.
cisticola (Cisticola), 465.
Cistothorus, 505.
citrina (Phaeochlaena), 508.
citrinella (Emberiza), 180.
citrinus (Turdus), 476.
Cladocera, 23.
Cladocerotis, 23, 24.
Clangula, 145, 219.
clangula(Bucephala), 144, 218, 332.
clara (Anisodes), 302.
— (Brachycola), 302.
— (Zosterops), 435.
clarkei (Turdus), 191, 477.
clavipalpis (Athctis), 19.
— (Phalaena), 19.
clementiae (Cinnyris), 427.
Cleophana, 50, 56-71.
clericalis (Pentholaea), 472.
Climacteris, 439.
Clivicola, 154.
Cloantha, 61.
cluentius (Cocytius). 361.
clypeata (Spatula), 143, 214.
Clytie, 105, 106.
Clytomyias, 456.
coangulata (Scopula), 292.
Coccothraustes, 157, 176.
coccothraustes (Coccothraustes), 176.
cochylioides (Eublemrna), 79.
— (Micra), 79.
cockerelli (Rbipidura), 498.
Cocytius, 361, 362, 363.
codeti (Ammetopa), 49, 50.
codeti (Bryomima), 50.
— (Metopoceras), 49, 50.
coelebs (Fringilla), 179.
coffeae (Nyceryx), 400.
coibae (Cyclorhis), 456.
colchicus (Phasianus), 251.
collaris (Alcippe), 481.
— (Apalis), 460.
— (Prunella), 503.
Colluricincla, 453.
collurio (Lanius), 186.
collybita (Phylloscopus), 188, 463.
Coloeus, 174.
colonus (Myiagra), 500.
— (Rhinomyias), 499.
Colophasia, 64.
coloratus (Calcarius), 155.
coltarti (Stachyris), 481.
Columba, 231.
columba (Uria), 130.
columbarius (Falco), 149, 202.
columbianus (Turdus), 475.
Colymbus, 129, 130, 230.
comes (Agrotis), 34.
— (Noctua), 34.
Comibaena, 299.
comma (Cirphis), 115.
comminutus (Dryocopus), 198.
communis (Sylvia), 190.
Comostola, 267.
Comostolopsis, 267.
compar (Pachycephala), 445.
compta (Miselia), 47.
concolor (Epunda), 53.
confusa (Calliope), 474.
— (Eublemrna), 84.
— (Luscinia), 474.
congrua (Cirphis), 11.
— (Noctua), 11.
coniades (Trochiodes), 508.
Conistra, 40.
conistrota (Catablemma), 83.
conjuncta (Catocala), 101.
— (Myonia), 508.
conspersa (Miselia), 48.
— (Phalaena), 48.
constanti (Agrotis), 29.
— (Euxoa), 29.
constrigilis (Platysphinx), 163, 164.
contempta (Pachycephala), 448.
contemptus (Turdus), 476.
continentalis (Xylophanes), 409.
contramutata (Scopula), 289.
conversa (Catocala), 101.
— (Noctua), 101.
Copicuuullia, 7, 63.
Copiphana, 67.
oora (Anisodes), 303.
520
cora(Brachycola), 303,
Coracias, 330.
corallipes (Callisitta), 440.
corallipes (Dendrophila). 440.
— (Sitta), 440.
coras (Trochiodes), 508.
corax (Corvus), 158, 173.
cornicalis (Nodaria), 113.
— (Phalaena), 113.
corniculata (Fratercula), 131.
comix (Corvus), 173.
coronata (Ifrita), 483.
coronatus (Pkyllergates), 468.
corone (Corvius), 174.
corsa (Certhia), 438.
cortex (Pkysopterus), 262.
corticea (Litosphingia), 510.
Cortyta, 93.
Corvus, 158, 173, 174.
Corythocichla, 481.
Corythus, 157.
Cosmia, 40, 41.
cosmius (Xylophanes), 412.
Cossypha, 470, 473.
costae (Certhia), 438.
costidentata (Phaeochlaena), 508.
Cosymbia, 271.
cotanoides (Elachyophthaluia), 325.
Coturnix, 251.
coturnix (Coturnix), 251.
Cracticus, 455.
crameri (Erinnyis), 385.
Craniophora, 7.
crassa (Corythocichla), 481.
— (Euxoa), 25.
— (Noctua), 25.
crassieornis (Pklogophora), 55.
— (Rhizotype), 55.
crassirostris (Erolia), 138.
— (Pseudozosterops), 437.
— (Zosterops), 437.
crassus (Turdinulus), 481.
Crateropus, 486.
crateroscelis, 482.
crecca (Anas), 142, 213.
cremorna (Catablemma), 83.
crepidatus (Stercorarius), 135.
cretica (Sesamia), 12, 13.
Crex, 249.
crex (Crex), 249.
crinalis (Herminia), 113.
— Pechipago), 113.
— (Zanclognatha), 113.
cristata (Prionops), 452.
cristatella (Aethia), 131.
cristatellua (Simorhynchus), 131.
cristatus (Podiceps), 224.
crocea (Eublemma), 84.
croccago (Phalaena), 40.
— (Xantholt'iiea), 40.
Croccthia, 138, 236.
Crosia, 112.
orotopezus (Turdus), 476.
cruda (Monima), 38.
— (Phalaena), 38.
cruentus (Pelicinius), 450.
— (Rhodophoneus), 450, 451.
cry ptan thus (Pomatorhinus). 488.
Cryptolopha, 462, 493, 501, 502.
Ctenodactylus, 506, 507.
cucullatus (Orthotomus), 467, 468.
— (Phyllergates), 467, 468.
Cucullia, 61-3.
Cuculus, 150, 151, 198, 330.
culex (Pipistrellus), 316.
Culicicapa, 500.
cunenensis (Calamocichla), 404.
cuppedius (Steatomys), 318.
curruca (.Sylvia), 190.
cursoria (Euxoa), 31.
— (Phalaena), 31.
curtisi (Anisodes), 303.
curvirostra (Loxia), 179.
curvirostris (Alauda), 329.
— (Certhilauda), 329.
— (Tyrannus), 329.
cyana (Pocilodryas), 491.
cyanea (Platysteira), 496.
cyaneus (Circus), 204.
cyanocephala (Todopsis), 457.
cyanocephalus (Todopsis), 457.
Cyanoderma, 480.
cyanoleuca (Myiagra), 500.
cyanopus (Numenius), 140.
cyanurus (Tarsiger), 154.
cyanus (Monticola), 475.
— (Poecilodryas), 494.
cycladum (Agrotis), 29.
— (Euxoa), 29.
cyclopea (Cleophana), 65.
— (Omia), 65.
Cyclorhis, 456.
Cygnus, 142, 209, 210.
cygnus (Cygnus), 142, 209.
Cylindroides, 264.
Cyllopoda, 311.
Cymatophora, 41.
Cyornis, 491, 492.
cypria (Rhodostrophia), 268.
Daoelo, 330.
.Ia]ir;i (Protoparrcl, 3liS.
daltoni (Myomya), 319.
— (Rattus), 319.
521
damarensis (Erythropygia). 47_.
Dammeria, 493.
daraineriana (Pachycophala), 448.
danncfaerdi (Miro), 494.
darceta (Pachylia), 387.
darollesi (Chariclea), 72.
— (Xylina), 72.
Dasystemum, 45.
daubei (Phytometra), S7.
— (Plusia), 87.
dayensis (Luperina), 44.
— (Palluperina), 44.
degener (Cinnyris), 427.
deglandi (Oidemia), 146.
deleta (Agropbila), 74.
— (Erastria), 74.
delicata (Gallinago), 242.
Delichon, 195.
deliciosa (Antitype), 52.
— (Polia), 52.
ck'inissus (Mecocerus), 261.
Dendrobiastes, 492, 493.
Dendrophila, 440.
delphinii (Xylina), 72.
deningeri (Turdus), 477.
Derthisa, 21.
deserta (Eublerama), 83.
— (Thalpocbares), 83.
deserti (Eublemma), 79.
— (Thalpocbares), 79.
deserticola (Arenostola), 14.
— (Calamia), 14.
— (Cardepia), 57.
— (Leptopoecile), 441.
— (Sylvia), 463.
Desniodilliscus, 317.
despectus (Pinarolestea), 453.
dewitzi (Aniaodes), 301.
— (Pisoraca), 301.
diacrisioidea (Harpagophana), 22.
Dianthoecia, 47, 111.
diapbora (Erastria), 77.
— (Eulocastra), 77.
Diaphoropbyia, 495.
Dicaeum, 328, 429, 430.
Dichonea, 60.
dicbrous (Pitohui), 454.
difficilis (Anisodes), 275.
— (Pisoraca), 275.
diffissa (Protoparce), 364.
diffluena (Cleopbana), 69, 70.
dilecta (Catocala), 99.
— (Mormonia), 99.
dilucida (Apopestea), 91.
— (Autopbila), 91.
— (Spintherops), 92.
diluta (Cleopbana), 66.
Diomedea, 135.
Dioptrornis, 489.
dipsaeea (Chloridea), 73.
— (Phalaena), 73.
discalis (Antitype), 53.
disconnexa (Tanaostyla), 508.
disjecta (Phyllophila), 78.
dispar (Pericyina), 93.
dispilota (Anisodes), 306.
dissentiens (Cinnyris), 427.
dissoluta (Arcbanara), 14.
— (Noctua), 14.
diasuasa (Trygodes), 270.
distigma (Atbetis), 112.
distincta (Acrobyla), 98.
— (Amphipyra), 90.
— (Parisoma), 495.
— (RWula), 110.
distinguenda (Agrotis), 31.
— (Euxoa), 31.
disturbans (Androphilua), 485.
diversum (Dicaeum), 429.
divisa (Bryopbila), 3.
dixoni (Oidemia), 146.
djamdjamensis (Alaeonax), 489.
— (Cisticola), 466.
— (Muscicapa), 489.
— (Pinarochroa), 471.
djampeana (Cyornis), 491, 492.
— (Siphia), 491.
dobertyi (Cbloropboneus), 451.
— (Elachyophthalma), 323.
— (Geocichla), 476.
— (Gerygone), 493.
— (Laniarius), 451.
— (Lophozosterops), 438.
— (Pitohui), 454.
— (Telophonus), 450.
— (Todopsis), 457.
— (Turdus), 476.
domesticus (Passer), 180.
domingonia (Erinnyis), 386.
dominicensis (Lanius), 329.
— (Saurothera), 330.
— (Tyrannus), 329.
dominicus (Charadrius), 136.
doreyana (Elachj'opbthalma), 325.
doufanae (Agrotis), 27.
— (Euxoa), 27.
Drasteria, 97.
dresseri (Parus), 185.
Drymoica, 467.
Dryobota, 60.
Dryobates, 151, 197.
Dryocopus, 198.
dubia (Antitype), 52.
— (Polia), 52.
dubium (Pbilentoma), 499.
dulcis (Argyrospila), 13.
522
dulcis (Malurun), 457.
dumasi (Geocichla), 476.
— (Pbyllergatea), 468.
— (Turdus), 476.
dumerilii (Noctua). 44.
— (Palluperina), 44.
duponchel (Cocytius), 362.
dnpraai (Pachyuromys), 313, 314.
dynaeus (Neogene), 343, 369.
dysodea (Hecatera), 48.
— (Miselia), 48.
Dyspbania, 265.
eacus (Pholus), 404.
Eafa, 431.
Earias, 115.
effusa (Amphipyra), 89.
— (Pyrois), 89.
eichhorni (Prasinocyma), 267.
Elachyopbthalma, 321, 322-6.
clacoides (Odontoptila), 279.
elara (Xylophanes), 414.
electra (Catocala), 100.
ello (Erinnyis), 334, 335, 385.
elocata (Catocala), 98.
— (Noctua), 98.
clongata (Oreozostcrops), 437.
— (Zosterops), 437.
Emberiza, 155, 180. 181, 331.
emiliae (Cblorocbaris), 437.
emini (Salpornis), 439.
emir (Bombycia), 54.
— (Eublemma), 83.
— (Thalpocharcs), 83.
emmae (Pratincola), 472.
Emmelia, 74.
emmides (Physopterus), 262.
Emmilites, 298.
Empusada, 63.
Enargia, 41.
encausta (Britbys), 15.
— (Noctua), 15.
endospila (Anisodes), 273.
— (Pisoraca), 273.
Enicurus, 474.
enucleator (Corytbus), 157.
— (Pinicola), 157.
Enyo, 397.
Eopsaltria, 444, 446.
cos (Agrotis), 29.
— (Euxoa), 29.
epapbus (Xylophanes), 412.
Ephesia, 101, 102.
ephialtes (Antbracia), 92.
— (Noctua), 92.
Ephialtias, 509.
Ephyra, 301.
Epia, 47. 111.
cpicoccastria (Anisodes). 304.
Epilecta, 34.
epilepidotus (Turdinulus), 481, 482.
Epimecia, 64.
Epipsilia, 31, 37, 42, 116.
Episema, 22, 23.
Epistor, 397-9.
epops (Upupa), 196.
Epunda, 53.
Erastria, 74, 76, 77.
Eremobia, 59.
eremocbroa (Homoptera), 93.
Eremomela, 461.
eremophila (Armada), 76.
— (Lipatephia), 76.
erinaria (Scopula), 281.
Erinnyis, 334, 335, 383-6.
Eriopus, 86.
Eritbacus, 194, 474.
erithacus (Cyornis), 492.
— (Siphia), 492.
Eritbrophaia, 73.
erlangeri (Cercomela), 471.
— (Phylloscopus), 463.
— (Zosterops). 432.
ernesti (Eublemma), 83.
Erolia, 137, 138, 235-7.
erubescena (Antarchaea), 109.
— (Protbymnia), 109.
erytbreae (Nilaus), 449.
erytbrinus (Carpodacus), 157.
erytlirypygia (Prunella), 503.
erytbrocepbala (Conistra), 40.
Erythrocichla, 482.
erythrogenys (Ciaticola), 466.
Erythromyias, 493.
erytbropleura (Zosterops), 437.
crytbropus (Tringa), 139, 329.
erytbropyga (Bracbypteryx), 479.
Erytbropygia, 472.
erythropygius (Accentor), 503.
erytbrosticta (Pomarea), 503.
erytbroxylea (Euxoa), 33.
— (Noctua), 33.
erytbrypygia (Prunella), 503.
Eublemma, 76, 77-86, 112.
Eulocastra, 77.
Eumegethes, 80.
Eumichtis, 53, 58-60.
Eumyias, 490, 491.
Eunctta, 143.
Eupetes, 488.
euphemia (Scopula), 281.
Eupborbia, 338.
eupborbiae (Celerio), 338.
Euprinodes, 460.
Eupk'xia, 56.
523
Eupyrrhoglossum, 400.
europaea (Sitta), 184, 439.
europaeus (Caprimulgus), 196.
euryclea (Protambulyx), 370.
Eurynorhynchua, 138.
eutychea (Catocala), 102.
— (Ephesia), 102.
Euxoa, 22-33.
euxoides (Athetis), 111.
everetti (Acanthopneuste), 461.
— (Androphilus), 485.
— (Cettia), 458.
— (Cryptolopha), 462.
— (Gerygone), 494.
— (Horeites), 458.
— (Mixornia), 480.
— (Monarcha), 502.
— (Pachycephala), 449.
— (Phyllergates), 468.
— (Pkylloscopus), 461.
— (Staphidia), 479.
exarninandus (Phylloscopus), 463.
examinata (Pachycephala), 446.
excelsior (Isognathus), 379.
excubitor (Lanius). 186.
excubitorius (Lanius), 452.
exigua (Laphyma), 20.
— (Noctua), 20.
exilis (Cisticola), 465.
expectata (Callisitta), 440.
exquisita (Cinnyris), 427.
exsiccata (Spintherops), 92.
— (Tathorhynchus), 92.
exsoleta (Axylia), 61.
— (Phalaena), 61.
exsul (Phylloscopus), 463.
— (Turdinulus), 482.
externalis (Nodaris), 113.
fabalis (Anser), 141, 211.
faceta (Epipsilia), 37.
— (Noctua), 37.
fadus (Sesia), 402.
falcata (Anas), 143.
— (Eunetta),J43.
Falcinellus, 328.
falcinellus (Plegadis), 208.
Falco, 148, 149, 200-2, 328.
falsalis (Nycteola), 114.
familiaris (Acrocephalus), 464.
— (Certhia), 184, 438, 439.
— (Oenanthe), 470.
— (Tatare), 464.
faroulti (Bryophila), 46.
— (Dasysternum), 45.
— (Epipsilia), 116.
— (Miselia), 48.
faroulti (Pachyuromys), 313, 314.
— (Polia), 48.
— (Procus), 46.
fasciatus (Pholus), 347, 405.
fasciolata (Pericyma), 93.
fasciolatus (Calamonastes), 465.
fassli (Tithraustes), 509.
fastidosus (Pomatorhinua), 488.
fastosus (Falcinellus), 328.
— (Promerops), 328.
fatimi (Cleophana), 68.
faustina (Anisodea), 304.
— (Perixera), 304.
felicina (Metopoceras), 49.
— (Polia), 49.
Felovia, 507.
feminina (Myiagra), 500.
fergussonis (Elachyophthalma), 321.
ferina (Nyroca), 144, 215.
ferrea (Oreicola), 471.
ferrocyanea (Myiagra), 500.
ferruginea (Casarca), 212.
— (Erolia), 138, 236.
— (Hemichelidon), 489.
— (Muscicapa), 489.
ferrugineus (Rhectes), 453.
festucae (Phytometra), 115.
ficua (Pachylia), 336, 337, 343, :i ; ,"
filigrama (MiseUa), 48.
— (Nocta), 48.
fimbria (Phalaena), 35.
— (Triphaena), 35.
fissipuncta (Sidemia), 38.
fixa (Synthymia), 86.
flabellicauda (Loxia), 331.
flammata (Josiomorpha), 509.
fiammatra (Agrotis), 36.
— (Phalaena), 36.
flammea (Bombyx), 55.
— (Rhizotype), 55.
fiammeus (Aaio), 150, 199.
flava (Athetis), 18.
— (Caradrina), 18.
— (Elachyophthalma), 322.
— (Gunda), 322.
— (Motacilla), 152, 182, 183.
flaveacens (Phylloscopua), 463.
flavicana (Macrosphenus), 484.
flavicincta (Antitype), 51.
— (Phalaena), 51.
flaviclunia (Dicaeum), 430.
flavicollis (Ixulus), 478.
flavicrinalia (Pechipago), 114.
flavida (Apalia), 460.
— (Euprinodea), 460.
flavifurfurata (Scopula), 290.
flavigaater (Microeca), 490.
Havigularis (Camaroptera), 459.
524
flavirena (Athetis), 18.
— (Caradrina), 18.
flavirostria (Carduelis), 177.
flavispila (Anisodes), 279.
— (Perixera), 279.
flavissirna (Zosteropa), 434.
flaviventer (Machaerirhyiichus), 500.
flaviventris (Cyclorhis), 456.
flavocincta (Apalis) 460.
flavogrisea (Pachycare), 444.
flavolivacea (Elachyophthalma), 323.
— (Horeites), 458.
flavonitens (Agrophila), 74.
florenciae (Artainus), 455.
floridana (Monarcha), 503.
— (Zosteropa), 436.
floridanua (Monarcha), 503.
floridensis (Dysphania), 265.
floris (Acanthopneuste), 462.
— (Brachypteryx), 479.
— (Cryptolopha), 501.
— (Phylloscopus); 462.
floriatan (Protoparce), 368.
flowed (Cisticola), 465.
foghaensis (Zosterops), 435.
fokiensis (Phylloscopus), 462.
Formicarius, 328, 329.
formosa (Anas), 143.
formosanus (Tarsiger), 473.
fortis (Microcichla), 474.
— (Pachycephala), 444.
Fratercula, 131, 248.
frenata (Cinnyria), 427.
Fringilla, 157, 179, 331.
frontalis (Callisitta), 440.
— (Dendrophila), 440.
— (Phoenicurus), 474.
— (Sitta), 440.
frugilegua (Corvus), 174.
Fulica, 250.
fulicariu3 (Phalaropus), 140. 239.
fuligula (Xyroca), 143, 216.
Fulmarus, 135.
fulva (Meganephira), 44.
— (Oria), 14.
— (Sidemia), 44.
— (Tapinostola), 14.
fulvescens (Turdinus), 484.
fulviventris (Pachycephala). iVJ.
fulvus (Charadrius), 136.
fumigatus (Turdus), 475.
funebris (Laniarius), 450.
funerea (Strix), 150.
funereus (Aegolius), 150.
furcata (Oceanodrouia), 135.
furuncula (Phalaena), 46.
— (Procus), 46.
furva (Dryobota), 60.
furva (Phalaena). 60.
fusca (Loxia), 331.
— (Oidemia). 146,220.
fuscater (Turdus), 477.
fuscatus (Turdus), 154.
fuscicapilla (Zosterops), 435.
fuscilinea (Cirphis), 10.
— (Leucania), 10.
fuscus (Larus), 246.
fustis (Hylinades). 263.
gabunensis (Neocoasyphus), 473.
gafsana (Cleophana), 67.
— (Copiphana), 67.
galactina (Dianthoecia), 47.
— (Miselia), 47.
galathca (Bryophila), 4.
galeata (Myiagra), 500.
galericulata (Aix), 214.
Gallinago, 136, 137, 241, 242.
gallinago (Gallinago), 136, 242.
— (Scolopax), 136.
GaUinula, 249.
— (Limnocryptes), 242.
galtoni (Saxicola), 470.
gambagae (Bessonornis), 470.
— (Cossypha), 470.
gamblei (Pachycephala). 445.
gamma (Phytometra), 88.
— (Phalaena), 88.
gannaacua (Amplypterus), 372.
Garrulax, 487.
Garrulua, 175.
garrulua (Bombycilla). 153, 187.
Gavia, 130.
geelvinkianum (Dicaeum), 429.
gelaatis (Larus), 134.
genibarbis (Thryothorua), 505.
gentflia (Accipiter), 205.
Geocichla, 476.
Geometra, 85.
geometrica (Grammodea), 107
— (Noctua), 107.
Gerbillus, 317.
germaini (Athetis), 15.
— (Bryophila), 15.
germana (Antitype), 53.
Gerygone, 493, 494.
geyri (Catablemma), 77.
— (Eublemma), 77.
gibraltariensis (Phoenicurus), 191.
giffardi (Cossypha), 473.
gigantea (Josia), 509.
gigaa (Alcedo), 330.
— (Dacelo), 330.
gilgit (Ianthocincla), 487.
— (Trochalopteron), 487.
525
gilvus (Mirnus), 477.
giulianettii (Phylloscopus), 461, 462.
glacialis (Fulmarus), 135.
glandarius (Garrulus), 175.
glarea (Anthophila), 85.
glareola (Tringa), 139, 237.
glaucescens (Larus), 132.
glaucus (Larus), 132.
Glottis, 139.
glottis (Totanus), 139.
glupisha (Fulmarus), 135.
goeldii (Protambulyx), 371.
— (Xylophanes), 411.
goliathina (Elachyophthalma), 324.
gonolek (Lanius), 331.
goodfellowi (Oreozosterops), 437.
— (Thryothorus), 505.
— (Turdus), 476.
— (Zosterops), 437.
goodsoni (Paohycephala), 448.
— (Phylloscopus), 462.
— (Staohyridopsis), 480.
— (Stachyris), 480.
gorgon (Epistor), 398.
grabae (Fratercula), 248.
gracilirostris (Calamociclila), 464.
gracilis (Artanius), 455.
— (Prinia), 457.
— (Taterillus), 317.
Gracula, 331.
graculus (Phalacrocorax), 222.
Grallaria, 329.
Grammodes, 107, 108.
Grarnniodia, 386.
Grammoscelis, 21.
granti (Turdinulus), 481.
graphidata (Scopula), 286.
Grapholitha, 61.
graslini (Luperina), 44.
— (Palluperina), 44.
— (Polyphaenis), 56.
grata (Anthophila), 81.
— (Eublemrua), 81.
graueri (Bradypterus), 469.
— (Cinnyris), 425.
— (Diaphorophyia), 495.
— (Laniarius), 451.
— (Prinia), 457.
— (Pseudocalyptomena), 496.
— (Turdus), 476.
Graueria, 484.
gravis (Puffinus), 223.
grebnitzkii (Hierofalco), 148.
grisea (Miselia), 112.
— (Polia), 112.
griseiceps (Microeca), 490.
— (Pachycephala), 446.
griseigena (Podiceps), 129, 225.
griseimargo (Eublemma), 78.
— (Leptosia), 78.
griseisticta (Muscicapa), 153.
griseiventris (Hylophilus), 456.
griseldis (Calamoherpe), 464.
griseogularis (Alseonax), 489.
— (Muscicapa), 489.
griseola (Hadula), 43.
— (Odontelia), 43.
griseonota (Pachycephala), 446.
griseonucha (Leucosticte), 156.
griseoviridis (Camaroptera), 459.
grisescens (Bryophila), 4.
grisescentior (Ianthocincla), 487.
grisola (Hyloterpe), 446, 447.
— (Pachycephala), 446, 447.
gubernator (Lanius), 451.
gueddelanea (Agrotis), 32.
— (Euxoa), 32.
guianensis (Pagamea), 349.
— (Xylophanes), 348, 349, 410.
guifsobalito (Lybius), 328, 330.
gularis (Mixornis), 480.
— (Rhinomyias), 499.
Gunda, 322.
gundi (Ctenodactylus), 507.
— (Mus), 506.
gustavi (Anthus), 151.
guttata (Stachyris), 480.
guttifer (Tringa), 139.
gutturalis (Cinnyris). 4i(i.
Gymnorhina, 454.
hachem (Crosia), 112.
Hadena, 51, 58, 59, 60, 111, 112.
Hadjina, 76.
Hadula, 21, 43.
haematidea (Arnathes), 39.
— (Noctua), 39.
haeinatocephala (Cisticola), 466.
Haematopus. 135, 233.
hagar (Antitype), 53.
hainanus (Parus), 443.
— (Pornatorhinus), 488.
— (Turdinulus), 482.
Haliaetus, 150, 206.
haliaetus (Pandion), 150, 207.
halinii (Athetis), 112.
— (Caradrina), 112.
Harnalia, 309.
hannibal (Protoparce), 365.
haringtoni (Oreicola), 471.
haringtoniae (Alcippe), 481.
— (Proparus), 481.
Harpagophana, 22.
Harpolestes, 449, 450.
harterti (Acanthopneuste), 462,
526
harterti (Anumeta), 95.
— (Artaniua), 455.
— (Camaroptera), 459.
— (Certhia), 439.
— (Ixulua), 478.
— (Massoutiera), 507.
— (Sigmodua), 452.
— (Zosterops), 435.
hartlaubi (Erythropygia). 472.
haatifera (Euxoa), 30.
haussa (Leggada), 319.
heba (Scopula), 295.
Heoatera, 48.
Heliophobua, 21, 22, 24.
Heliothia, 72, 73, 98.
hellniayri (Parua), 443.
helvola (Amathes), 39.
— (Phalaena), 39.
Hemeroplanea, 395, 396.
Heniichelidon, 489.
Henicurus, 474.
henkei (Anumeta), 95.
henrici (Dammeria), 493.
— (Dendrobiaates), 493.
— (Muscicapa), 493.
Herminia, 113.
Herpornis, 478.
Herse, 334, 347, 361.
heterolaemus (Phyllergatea), 468.
hiaticula (Charadriua), 234.
hibernana (Pratincola), 472.
— (Saxicola), 193, 472.
hibernicua (Cinclua), 504.
Hierofalco, 148.
kilaris (Catocala), 100.
hilgerti (Anumeta), 96.
— (Nilaua), 449.
— (Palpangula), 96.
— (Peliciniua), 450.
— (Rhodophoneus), 450.
Hippoaideroa, 315.
hirta (Noctua), 20.
— (Ulochlaena), 20.
Hirundo, 154, 195, 330.
hirundo (Sterna), 244.
hiapanica (Athetia), 17.
— (Caradrina), 17.
Hiatrionicua, 145, 219.
hiatrionicua (Hiatrionicua), 145, 219.
hodnae (Agrotia), 26.
— (Euxoa), 26.
hoggari (Euxoa), 27.
holboelli (Carduelis), 156, 177.
holboellii (Podieepa), 129.
Iiomaema (Scopula), 294.
homeyeri (Hyloterpe), 447.
— (Pachycephala). 447.
Homoptera, 93.
Horeitea, 458.
Houbaropaia, 331.
hulli (Mimua), 478.
— (Nesomimua), 478.
humei (Artamua), 455.
— (Turdinulus), 481.
hunteri (Ciaticola), 465.
hutchinsii (Branta), 141.
hyacinthina (Cyornis), 492.
hybris (Raphia), 98.
Hydrilla, 110.
Hydrobata, 504.
Hydrobatea, 223.
Hydrochelidon, 243.
Hydroecia, 42.
hyemalia (Clangula), 145, 219.
Hylophila, 115.
Hylophilua, 456.
Hyloterpe, 446, 447.
Hypaetra, 93.
Hypena, 113, 114.
hyperboreua (Anaer), 141.
— (Larus), 132.
hyperythra (Dendrobiaatea), 492, 493.
— (Muaeicapa), 492.
— (Muacieapula), 492, 493.
— (Pachycephala). 447.
Hypeuthina, 15.
Hypocryptadius, 438.
Hypoglaucitia, 94.
hypogrammica (Anthreptea), 429.
hypoleuca (Muscicapa), 187.
— (Tringa), 139, 237.
hypoleucus (Haliaetua), 150.
— (Thryothorus), 505.
Hypomecia, 64, 116.
hypomelaena (Squatarola). 136.
Hypothymia, 496.
hypoxantha (Ciaticola), 467.
— (Hyloterpe), 447.
— (Microeca), 490.
— (Pachycephala), 447.
Iambiodes, 76.
Ianthocincla, 487, 488.
iboenaia (Turdinua), 484.
Ifrita, 483.
ignicapillua (Regulua), 1S5.
ignipeta (Agrotis), 32.
— (Lycophotiaa), 32.
ijimae (Clivicola), 154.
— (Riparia), 154.
iliacus (Turdus), 191.
illunaris (Ciytie), 105.
illuatria (Nephele), .Ml'.
immer (Colymbus), 230.
impar (Cortyta), 93.
527
iinperator (Agrotis), 33.
— (Euxoa), 33.
implexa (Noctua), 51.
implexa (Scologramnia), 51.
inactuosa (Scopula), 296.
inaestimata (Cinnyris). 426.
incana (Tringa), 139.
incarnata (Noctua), 72.
— (Rhodocleptria), 72.
incerta (Bryophila), 76.
— (Iambiodes), 76.
incumbens (Anisodes), 304.
indioa (Houbaropsis), 331.
— (Otis), 331.
— (Tarsiger), 473.
indicus (Enicurus), 474.
— (Tarsiger), 473.
indigo (Eumyias), 491.
iners (Anisodes), 271.
— (Pisoraca), 271.
inexpeetata (Cistecola), 465.
inexpectatus (Prionochilus), 430.
infraluteola (Elachyophthalma), 325.
infrenata (Cinnyris), 426.
ingrata (Athetis), 18.
— (Caradrina), 18.
innexa (Dendrobiastes), 492.
— (Muscicapa), 492.
— (Siphia), 492.
inomata (Eopsaltria), 446.
— (Gerygone), 494.
— (Pachycephala), 446.
inquinata (Centropodia), 51.
— (Hadena), 51.
insana (Cerocala), 108, 109.
— (Graminodes), 108.
insignis (Aesalon), 149.
— ■ (Clytomyias), 457.
— (Falco), 149.
insincera (Scopula), 280.
insitiva (Anisodes), 275.
— (Pisoraca), 275.
insulana (Earias), 115.
— (Tortrix), 115.
insularis (Parus), 444.
— (Zethes), 110.
— (Zosterops), 436.
insularum (Elachyophtbalma), 324.
intensior (Anthreptes), 429.
intercedens (Lanius), 452.
intermedia (Catocala), 101.
— (Triphaena). 35.
— (Zosterops), 433, 434.
intermixta (Phytometra), 88.
internata (Scopula), 293.
interni (Regulus), 441.
interposita (HerpoTiis), 478.
— (Rhipidura), 498.
interpositus (Malaconotus), 452.
interpres (Arenaria), 136.
intricatus (Horeites), 458.
inturbida (Elachyophthalma). 322.
— (Leucoma), 322.
inumbrata (Agrotis), 16.
— (Athetis), 16.
imius (Heineroplanes), 396.
iphis (Aleuron), 397.
irregularis (Lipotaxia), 269.
irrisor (Cardepia), 57, 58.
irritaria (Apamea), 43.
— (Margelana), 43.
islandicus (Troglodytes), 601.
islyana (Agrotis), 30.
— (Euxoa), 30.
Isognathus, 343, 349, 375-82.
isolata (Scopula), 281.
ispida (Alcedo), 197.
italiae (Aegithalos), 442.
Ixobryehus, 209,
Ixulus, 478.
jacksoni (Bathmocercus), 483.
jacobsi (Athetis), 19.
jakuschima (Muscicapa), 490.
— (Zanthopygia), 490.
janeira (Cyllopoda), 311.
jansei (Xenosphingia), 168, 169, 512.
janthina (Triphaena), 35.
japix (Enyo), 397.
japonica (Certhia), 438.
— (Zosterops), 436, 437.
japonieus (Anthus), 152.
— (Coccothraustes), 157.
javanica (Oreozosterops), 437.
— (Zosterops), 437,
jocosa (Anisodes), 302.
— (Brachycola), 302.
johannae (Prionochilus), 431.
johni (Pachyeephala), 445.
jordani (Catamecia), 65.
— (Enargia), 41.
Jortyna, 42.
josephae (Vireo), 455.
Josia, 509.
jubaensis (Zosterops), 432.
jubata (Cleophana), 66.
jucunda (Eublemma), 85.
— (Noctua), 85.
jugularis (Cinnyris), 426.
Jugurthia, 6.
juliae (Arachnothera), 428.
juventina (Eriopus), 86.
— (Phalaena), 86.
Jynx, 198.
528
kaaba (Agrotis), 32.
— (Euxoa), 32.
kabylaria (Leucanitis), 97.
kabylorum (Troglodytes), 504.
kadeni (Oryba), 344, 347, 389.
kadenii (Athetis), 17.
kaffensis (Zosterops), 433.
kalaoensis (Cyornis), 491, 492.
— (Siphia), 491.
kalulongae (Setaria), 482.
kaintschatica (Pyrrhula), 157.
kamtschaticus (Dryobates), 151.
kamtschatkensis (Corythus), 157.
— (Parus), 158.
— (Pinicola), 157.
kebeae (Elackyophthalma), 322.
— (Gunda), 322.
keiensis (Cinnyris), 427.
— (Elachyophthalma), 322.
kerraesina (Lycopbotia), 10.
— (Noctua), 10.
kettlewelli (Macronus). 479.
kbalildja (Metopoceras), 51.
kikuyuensis (Crateropus), 486.
kisserensis (Gerygone), 494.
Kittacincla, 473.
kivuensis (Turdinus), 483.
kleinschniidti (Parus), 185, 443.
kowaldi (Ifrita), 483.
— (Todopsis), 483.
kraussi (Calophasia), 70.
kuebni (Pacbycephala), 446.
kiilmi (Cyornis), 492.
— (Dicaeura), 429.
■ — (Gerygone), 494.
— (Zosterops), 436.
kulambangrae (Monareba), 502.
— (Zosterops), 436.
labruscae (Peacus), 347.
— (Pholus), 406.
laeernaria (Eublemma), 85.
— (Georaetra), 85.
lacroixi (Armada), 76.
Iacteola (Eublemma), 84.
lacuum (Crateropus), 486.
— (Parus), 444.
laeta (Catocala), 99.
— (Mormonia), 99.
laetissima (Mieroeca), 490.
Lagopus, 148.
lagopus (Buteo), 149, 203.
languida (Leueania), 10.
Laniarius, 450, 451.
Lanius, 186, 329, 331, 451, 452.
Lapbyma, 20.
lapidea (Grapholitha), 61
lapponica (Limosa), 138, 240.
lapponicus (Calcarius), 155.
Larus, 132^, 244-6, 331.
Larvivora, 474.
lassauxi (Erinnyis), 384.
lasserrei (Euxoa), 24.
— (Luperina), 24.
lata (Agrotis), 26.
— (Euxoa), 26.
lateralis (Zosterops), 433.
latitans (Emmilitis), 298.
— (Scopula), 298.
latoucbii (Aethopyga), 425.
latreillei (Eriopus), 86.
— (Noctua), 86.
lautus (Polyptycbus), 167.
lavellae (Rhipidura), 498.
leacbi (Isognathus), 378.
Leggada, 319.
leonbardi (Euplexia), 56.
Leptopoecile, 441.
leptorbyncba (Calamocichla), 464.
Leptosia, 78.
lescbenaulti (Enicurus), 474.
Leueania, 9, 10, 11.
Leucanitis, 97.
Leucoeblaena, 22, 23.
leucogaster (Agrotis), 36.
— (Cinolus), 504.
— (Noetua), 36.
— (Paobycepbala), 445.
Leucolepis, 329.
Leueoma, 322.
leueomelas (Catepbia), 95.
— (Phalaena), 95
leucopbaea (Crocethia), 236.
— (Luperina), 56.
— (Phalaena), 56.
leucophrys (Sylvietta), 460.
leucopogou (Prinia), 457.
leucops (Poecilodryas), 495.
— (Tregellasia), 495.
leucoptera (Cortyta), 93.
— (Hypaetra), 93.
leucopyga (Oenantbe), 470.
leucopygialis (Artamus), 455.
leucopygius (Crateropus), 486.
Leucorhampha, 391, 392.
leucorbynchus (Artamus), 455.
leucorrboa (Oceanodroma), 135, 223.
— (Oenantbe), 192.
Leueosticte, 156.
leueostriatus (Motacilla), 152.
leucotis (Anas), 332.
— (Stachyris), 48().
— (Vireolanius), 456.
leucura (Eopsaltiia), 444.
leucurus (Oenanthe), 471
529
leucurua (Saxicola), 471.
levaillanti (Corvua), 158.
libanotica (ApopeBtea), 91.
— (Autophila), 91.
libatrix (Phalaena), 89.
— (Scoliopteryx), 89.
Libyoclania, 167, 168.
licaon (Pholus), 403.
liohenea (Eumichtis), 53.
— (Noctua), 53.
ligaminoaa (Autophila), 91.
— (Spintheropa), 91.
lilacea (Callisitta), 440.
— (Dendrophila), 440.
Limnocryptea, 242.
Limoaa, 138, 139, 240.
limoaa (Limoaa), 139, 240.
linaria (Carduelia), 156, 177, 178.
lineatum (Ianthocincla), 487.
— (Trochalopteron), 487.
linogriaea (Agrotia), 34.
Lioptilua, 483.
lipara (Agrotia), 24.
— (Euxoa), 24.
Lipatephia, 76.
Lipotaxia, 269, 270.
lithargyria (Sideridie), 9.
Lithocampa, 60.
Lithophane, 61.
lithorhiza (Xylocampa), 60.
Lithoatege, 312.
lithoxylea (Hypomeoia), 116.
— (Pseudomecia), 116.
Litoaphingia, 510.
littoralis (Scelolophia), 307.
litura Amathea). 39.
— (Noctua), 20.
— (Phalaena), 39.
— (Prodenia), 20.
livia (Coluraba), 231.
lividalia (Hypena), 114.
— (Ophiuche). 114.
lobatus (Phalaropua), 140, 240.
Lobocleta, 309, 310.
Loouatella, 153, 188.
loelia (Xylophanea), 349, 414.
lomvia (Uria), 130.
longicauda (Pipra), 331.
longicaudua (Stercorariua), 135.
longipennis (Sterna), 132.
longiroatris (Araohnothera), 427, 42a.
— (Cuculus), 330.
— (Gymnorhina), 454.
— (Saurothera), 330.
longmari (Arachnothera), 428.
Lophoterges, 60.
Lophozoateropa, 438.
loreyi (Cirphia), 10.
36
loreyi (Noctua), 10.
lota (Amathea), 38.
— (Phalaena), 38.
louiaiadenais (Rhipidura), 496.
Loxia, 179, 330, 331.
Lucanitis, 98.
lucida (Amathes), 39.
— (Bytharia), 306.
— (Noctua), 74.
— (Phalaena), 39.
— (Tarache), 74.
lucifer (Cocytiua), 363.
lueipara (Euplexia), 56.
lucipeta (Euxoa), 32.
— (Phalaena), 32.
luctuoaa (Acontia), 75.
— (Phalaena), 75.
lugena (Cyllopoda), 311.
— (Motacilla), 153.
lugubria (Ciaticola), 466.
— (Epiator), 397.
— (Motacilla), 183.
— (Parus), 442.
Lullula, 182.
lunaris (Minucia), 105.
— (Phalaena), 105.
— (Pseudophia), 105.
Lunda, 131.
lunosa (Noctua), 39.
— (Omphaloacelia), 39.
Luperina, 23, 24, 44, 56.
lusca (Perigonia), 400.
Luscinia, 154, 194, 474.
luscinioidea (Loouatella), 188.
Luaciniola, 469.
lusitanica (Cleophana), 70.
luteago (Miaelia), 42.
— (Phalaena), 42.
lutearia (Ephyra), 301.
luteiro8tria (Zoateropa), 436.
luteocinnamomea (Miaelia), 110.
luteonigra (Clytie), 106.
lutoaa (Agrotia), 34.
— (Epilecta), 34.
luzonienae (Dicaeum), 429, 430.
luzonienaia (Dendrobiaatea), 493.
— (Muscicapa), 444.
— (Muacicapula), 493.
Lybius, 328, 330.
lychnidia (Amathea), 38.
— (Phalaena), 38.
Lycophotia, 8, 16, 28, 32, 37.
lycophotioides (Epipailia), 37.
— (Euxoa), 37.
Lycophotiaa, 32.
Lyrurua, 250.
mabillei (Areno8tola), 14.
530
mabillei (Tapinostola), 14.
Machaerirhyiichu3, 500, 501.
macilenta (Amathea), 38.
— (Nootua), 38.
mackloti (Dicaeum), 429.
Macronus, 479, 480.
macrorhynchua (Nucifraga), 174.
Macroaphenus, 484.
macrura (Sterna), 131.
macrurua (Kittacincla), 473.
niaculata (Eafa), 431.
— (Erolia), 137.
— (Rhamphocharia), 431.
— (Tringa), 137.
maculator (Xylopbanea), 414.
maculatua (Anthus), 152.
maderenaia (Coaymbia), 271.
Madoryx, 393-5.
maeonia (Bryopbila), 111.
Mageutica, 94.
magna (Nyctala), 150.
magnifica (Derthisa), 21.
— (Grammoacelia), 21,
magniroatria (Gerygone), 494.
— (Neoaitta), 440.
magnolii (Diantboecia), 47.
— (Miaelia), 47.
magnua (Aegobua), 150.
mabrattarum (Parua), 443.
major (Anumeta), 95.
— (Cbloropeta), 495.
— (Dryobatea), 151, 197.
— (Larus), 133.
— (Parua), 184, 442, 443.
malaccenaia (Arjthreptea), 428.
Malacocincla, 483, 484.
Malaconotua, 452.
Malacopterum, 482.
malayana (Siva), 479.
malenaia (Apalia), 460.
— (Euprinodea), 460.
Malurua, 457.
malvae (Noctua), 73.
— (Xantbodes), 73.
Mariieatra, 42, 43, 47, 58.
mancipium (Tanagra), 331.
Mania, 90.
manaoura (Agrotia), 8.
— (Lycopbutia), 8.
manumudari (Monarcba), 502.
margaritacea (Lycopbotia), 37.
— (Noctua), 37.
margaritoaa (Lycopbotia), 28.
— (Noctua), 28.
Margelana, 43.
marginata (Cesticola), 466.
mariae-ludovicae (Aglossestra), 21.
— (Hadula), 21.
mariac (Urolaia), 461.
marila (Cinclus), 504.
— (Hydrobata), 504.
— (Nyroca), 143, 217, 332.
mariloides (Nyroca), 143.
marinua (Larua), 246.
maritima (Erolia), 137.
marmoratua (Bracbyrbamphus), 130.
marocana (Cleopbana), 70.
maroccana (Sylvia), 463.
marsdeni (Heliopbobua), 22.
martinica (Cbaetura), 330.
— (Hirundo), 330.
martinua (Gracula), 331.
inartius (Dryocopua), 198.
masaoni (Ctenodactylua), 506, 507.
Masaoutiera, 507.
Mastomya, 319.
mathewai (Acanthiza), 461.
maura (Apopeatea), 90.
— (Autopbila), 91.
— (Mania), 90.
— (Minucia), 105.
— (P8eudopbia), 105.
— (Spintberops), 91.
mauretaniae (Cleopbana), 69.
mauretanica (Agrotis), 31.
— (Cardepia), 58.
— (Catamecia), 3, 65.
— (Certbia), 439.
— (Euxoa), 31.
mauritanicus (Turdua), 477.
mauritii (Lanius), 452.
maxima (Leucosticte), 156.
— (Montifringilla), 156.
maximua (Larua), 331.
Mecocerua, 260, 261.
media (Gallinago), 241.
medor (Cocytiua), 362.
meeki (Elacbyopbthalma), 323.
— (Monarcba), 502.
— (Pacbycepbala), 445.
— (Pitohui), 453.
— (Pristorbampbua), 431.
— (Sericornis) 461.
— (Zoateropa), 435.
Megalornis, 140.
Meganepbira, 44, 55.
megarhyncba (Luacinia), 194.
— (Pinarolestea), 453.
megarbyncbus (Monarcba), 503.
megaatoma (Uicaeum), 430.
megaxantha (Artaxa), 321.
— (Elacbyopbthalma), 321.
melaniprosopus (Cblorophoneua), 451.
Melanobucco, 328, 330.
melanocepbala (Anaa), 332.
melanoleuca (Elacbyopbthalma), 324.
531
melanonota (Pachycephala), 447.
melanope (Motacilla), 152.
melanothorax (Cyanoderrna), 480.
melanotis (Mimua), 478.
melanura (Cercomela), 471.
— (Pachycephala), 448.
melanuroides (Limosa), 139.
Melicleptria, 73.
melophilus (Erithacus), 194, 474.
melvillensis (Artauius), 455.
menechus (Isognathus), 379.
meridae (Cistotkorus), 505.
meridionalis (Climacteris), 439.
Mergus, 147, 220, 221.
merganser (Mergus), 147, 220.
Merula, 476.
merula (Turdus), 192, 477.
mesotoma (Anisodes), 276.
— (Pisoraca). 276.
messaouda (Euxoa), 23.
— (Luperina), 23.
Metachrostis, 6.
Metalloehlora, 266.
Metapistis, 71.
Metasiopsis, 309.
raeticulosa (Phalaena), 55.
— (Trigonophora), 55.
Metopoceras, 49-51.
Metoptria, 86.
metria (Lilryoclanis), 167, 168.
raeyeri (CinnjTis), 426.
— (Pitohui), 453.
Micra, 79.
Microcichla, 474.
Microeca, 490.
Microloxia, 300.
Micropus, 444.
mikettae (Vireolanius), 456.
milherei (Lithocampa), 60.
— (Lophoterges), 60.
Milvus, 205.
milvus (Milvus), 205.
mimicaria (Cimelia), 89.
— (Protomeceras), 89.
mimiocotana (Elachyophthalma), 326.
Mimus, 477, 478.
mindanensis (Cryptolopha), 501.
— (Ptilocichla), 482.
— (Ptilopyga), 482.
mindorensis (Brachypteryx), 479.
ministra (Fringilla), 331.
minor (Dryocopus), 198.
— (Harpolestes), 450.
— (Nilaus), 449.
— (Odontorhynchus), 505.
Minucia, 105.
minullum (Dicaeum), 430.
minuta (Erolia), 236.
minutus (Ixobrychus), 209.
mira (Athene), 199.
mirandae (Vireo), 455.
Miro, 494.
Miselia, 110, 111, 112, 116, 42-6, 48, 58.
misera (Metalloehlora), 266.
raisimae (Pachycephala), 448.
misisippica (Tanagra), 331.
mistacea (Prinia), 457.
Mixornis, 480.
modestus (Mecocerus), 261.
modularis (Accentor), 503.
— (Prunella), 194, 503.
molitor (Polyptychus), 159, 167.
moloneyanus (Turdinus), 484.
Momonipta, 508.
Monarcha, 502, 503.
monedula (Coloeus), 174.
mongolus (Charadrius), 136.
Monima, 38.
monochroma (Eumichtis), 59.
— (Phalaena), 59.
monoglypha (Parastichtis), 42.
— (Phalaena), 42.
monogramma (Metoptria), 86.
montana (Mixornis), 480.
montanus (Horeites), 458.
— (Parus), 443.
— (Passer), 180.
Monticola, 475.
monticola (Pitohui), 454.
Montifringilla, 156.
montifringilla (Fringilla), 157, 179.
montis (Bradypterus), 469.
— (Cryptolopha), 501.
— (Stasiasticus), 469.
morinellus (Charadrius), 234.
Mormonia, 99.
moroka (Pachycephala), 446.
morosa (Metopoceras), 51.
moses (Hypoglaucitis), 94.
mossi (Isognathus), 380.
— (Xylophanes), 348, 349, 408.
Motacilla, 152, 153, 154, 1S2-4, 331.
mozabitica (Eublemma), 78.
muelleri (Cisticola), 467.
inultigruma (Comibaena), 299.
mmalis (Bryophila), 5.
— (Phalaena), 5.
murina (Alseonax), 489.
— (Crateroscelis), 482.
— (Muscicapa), 489.
murinus (Alseonax), 489.
— (Bathmocercus), 483.
muriicolor (Euxoa), 24.
Mus, 506.
Muscicapa, 153, 187, 329, 444. 489-92.
muscicapinus (Bradyornis). 489.
532
Muscicapula, 492, 493.
musculosa (Argyrospila), 8.
— (Noctua), 8.
musculus (Aegithalus), 441.
— (Androphilus), 485.
— (Anthoscopus), 441.
musiea (Leucolepis), 329.
musicus (Formicarius), 329.
— (Turdus), 191.
mustapha (Dichonia), 60.
— (Xylocampa), 60.
mutus (Lagopus), 148.
HJyiagra, 500.
Myiophoneus, 479.
Myomys, 319.
Myonia, 508.
Myrmornis, 328, 329.
Myrmothera, 329.
Myrmotherula, 329.
mysoriense (Dicaeum), 429.
Mythimna, 76.
mytilene (Emberiza), 331.
mzabi (Massoutiera), 507.
naevia (Locustella), 188.
Namaugana, 45.
nana (Acanthiza), 461.
narcissina (Muscicapa), 490.
— (Zanthopygia), 490.
natalensis (Chloropeta), 495.
— (Cisticola), 465.
natronensis (Pachyuromys), 314.
natunensis (Stachyris), 481.
nearctica (Nyroea), 143.
nebularia (Tringa), 139, 239.
nebularius (Glottis), 139.
— (Totanus), 139.
nebulifera (Ptochophyle), 270.
nechus (Xylophanes), 412.
neglecta (Gerygone), 493.
neglectum (Aleuron), 397.
— (Dicaeum), 429.
negroides (Dendrobiastes), 492.
— (Muscicapula), 492.
nehrkorni (Micropus), 444.
nelvai (Eublemma), 112.
— (Rabinopteryx), 64.
Neocossyphus, 473.
Neogene, 343, 369, 440.
Nephele, 512.
Nereisana, 76.
Neromia, 299.
Nesomimus, 478.
Netta, 215.
neuraanni (Cisticola), 465.
— ( Sylvietta), 460.
neumayer (Sitta), 440.
neurica (Archanara), 14.
— (Noctua), 14.
newtoni (Parus), 1S4.
ni (Noctua), 88.
— (Phytometra), 88.
niasensis (Aethopyga), 425.
nickerlii (Apamea), 44.
— (Luperina), 44.
— (Palluperina), 44.
niger (Parus). 444.
nigeriae (Gerbillus), 317.
nigra (Aporophyla), 54.
— (Hydrochelidon), 243.
— (Noctua), 54.
— (Oidemia), 147, 219.
nigricans (Branta), 142.
nigriceps (Apalis), 460.
— (Stachyris), 481.
nigricollis (Podiceps), 226.
nigrilore (Dicaeum), 430.
nigriloris (Eumyias), 490.
— (Stoparola), 490.
nigrimentalis (Stoparola), 490.
nigripectus (Machaerirhynchus), 501.
nigriventris (Poecilodryas), 494.
nigrocincta (Antitype), 52.
— (Polia), 52.
nigrocinnamomea (Rhipidura), 498.
nigromentalis (Rhipidura), 497.
nigro-orbitalis (Poecilpdryas), 495.
— (Tregellasia), 495.
nigrorum (Dendrobiastes), 493.
— (Muscicapula), 493.
nigrotectus (Monarcha), 503.
nigrum (Agrotis), 35.
— (Phalaena), 35.
Nilaus, 449.
nilotica (Sylvietta), 460.
nipalensis (Proparus), 481.
nisseni (Agrotis), 36.
— (Ammetopa), 49, 50.
— (Bryomima), 50.
— (Parascotia), 110.
nisus (Accipiter), 205.
nitida (Temnora), 160, 161.
nitidissima (Scopula), 289.
nivalis (Plectrophenax), 155, 181.
nivea (Procnias), 330.
niveiventris (Rhipidura), 497.
noctambulatrix (Cladocerotis),
— (Euxoa), 23.
Noctua, 4, 5-17, 20-40, 61, 92,
— (Athene), 199.
Nodaria, 113.
nodosalis (Herminia), 113.
nomius (Hermeroplanes), 395.
nona (Agrotis), 34.
novaeguineae (Alcedo), 330.
23.
,98.
533
novaeguineae (Dacelo), 330.
novus (Machaerirhynchus), 500,
nubigera (Chloridea), 72.
— (Heliothis), 72.
Nucifraga, 174.
nudicollia (Procniaa), 329.
nudigula (Pachycephala), 445.
Numenius, 140, 241.
numerica (Agrophila), 77.
— (Phyllophila), 77, 78.
numida (Hypeuthina), 15.
— (Stilbia), 15.
nupta (Myiagra), 500.
Nyceryx, 400.
Nycroca, 332.
Nyctala, 150.
Nyctea, 150, 199.
nyctea (Nyctea), 150, 199.
Nycteola, 114.
Nycticorax, 208.
nycticorax (Nycticorax), 208.
nymphaea (Epheaia), 101.
— (Noctua), 101.
nymphagoga (Catocala), 104.
Nyroca, 143, 144, 215-17.
nyroca (Nyroca), 216.
obelisca (Euxoa), 30.
— (Phalaena), 30.
oberholseri (Hypothymis), 496.
oberthuri (Athetis), 18.
— (Catocala), 99.
— (Copicucullia), 7.
— (Cucullia), 62.
— (Omia), 65.
— (Sidemia), 38.
— (Simyra), 7.
obesa (Euxoa), 24.
obiensis (Eumyias). 491.
— (Stoparola), 491.
obliquua (Pholus), 404.
obscura (Burnesia), 457.
— (Erinnyis), 386.
— (Prinia), 457.
— (Rhizotype), 55.
obscurior (Pachycephala), 447.
obacurus (Parus), 184.
— (Turdus), 154.
obaitalis (Hypena), 113.
— (Pyralis), 113.
obsoleta (Chloridea), 73.
— (Leucania), 12.
— (Noctua), 12, 73.
obsoletus (Turdus), 475.
obstinatus (Zosterops), 434, 435.
occidentaliB (Accentor), 503.
— (Ianthocincla), 488.
occidentalis (Microeca), 490.
— (Prunella), 194, 503.
Oceanodroma, 135, 223.
ocellulata (Comostola), 267.
ochotensis (Acrocephalus), 153.
— (Locustella), 153.
ochraceicepa (Hylophilus), 456.
ochreimacula (Cloanthia), 61.
— (Grapholitha), 61.
ochricrinita (Scopula), 287.
ochrifrons (Scopula), 288.
ochropus (Tringa), 238.
ochrurua (Phoenicurus), 194.
ockendeni (Aniaodea), 303.
— (Turdus), 477.
ocularia (MotacuTa), 153.
ocypete (Epistor), 398.
oditis (Leucochlaena), 22.
— (Noctua), 22.
odius (Aganisthoa), 343.
Odontelia, 43.
Odontoptila, 279.
Odontorhynchua, 505.
Oederemia, 6.
Oedibrya, 6.
oedicnemua (Burhinus), 233.
Oenanthe, 154, 192, 470, 471.
oenanthe (Motacilla), 154.
— (Oenanthe), 154, 192, 471.
oenaa (Columba), 231.
oenotrua (Erianyia), 385.
ogliaatrae (Parua), 442.
oiclua (Madoryx), 393.
Oidemia, 146, 147, 219, 220.
okinawae (Parua), 443.
okinawensia (Scopula), 289.
oleagina (Bombyx), 54.
— (Valeria), 54.
oleracea (Miselia), 58.
olivacea (Sericornis), 461.
olivaceua (Turdus), 476.
oliveacena (Organopoda), 268.
oliveta (Scopula), 283.
olor (Cygnua), 210.
omar (Cleophana), 50.
— (Metopoceraa), 50.
Omia, 65.
omisaa (Cyornia), 491, 492.
— (Kittacincla), 473.
— (Siphia), 491.
omoensia (Crateropus), 486.
— (Oenanthe), 470.
— (Prionopa), 452.
— (Saxicola), 470.
— (Zosterops), 432.
omphaleae (Erinnyis), 384.
Omphalophana, 66, 70.
Omphaloacelia, 23, 39.
S34
onerosa (Gerygone), 494.
oorti (Clytomyias), 457.
— (Sericornis), 461.
oothesia (Anisodes), 272.
— (Pisoraca), 272.
Ophinche, 114.
Ophiusa, 107.
ophthalmica (Scopula), 284.
opperta (Scopula), 308.
Opsiphanes, 343.
optabilis (Heliophobus), 24.
optata (Catocala), 100, 102.
optatus (Cuculus), 151.
orana (Cladocera), 23.
— (Episema), 23.
— (Leucochlaena), 23.
oranaria (Agrotis), 31.
— (Ckesias), 76.
— (Euxoa), 31.
— (Nereisana), 76.
oranensis (Drasteria), 97.
orbiculata (Organopoda), 268.
orbifera (Semaeopus), 269.
orbona (Agrotis), 34.
— (Phalaena), 34.
— (Triphaena), 34.
Oreicola, 471.
oicophila (Cettia), 458.
oreophilus (Horeitcs), 458.
Oreozosterops, 437.
Organopoda, 268.
Oria, 14.
orichalcea (Noctua), 87.
— (Phytometra), 87.
Oricia, 509.
orientalis (Hydroccia), 42.
— (Jortyna), 42.
Oriolus, 175, 331.
oriolus (Oriolus), 175.
oritis (Cinnyris). 426.
ornatus (Leucorhampha), 392.
orpheus (Pachycephala), 446.
Orrhodia, 40.
ortbographus (Polyptycbus), 159.
Orthosia, 37.
Orthotomus, 467, 468.
Oiyba, 344, 389, 390.
oscillans (Microeca), 490.
osculans (Haematopus), 135.
osmastoni (Horeitcs), 458.
ostralegus (Haematopus), 135, 2:M.
ostrina (Eublemma), 80.
— (Noctua), 80.
Otis, 331.
otus (Asio), 199.
oustaleti (Ianthocincla), 488.
— (Trochalopteron), 488.
ovata (Xcnorma), 509.
owstoni (Aethopyga), 425.
— (Ianthooincla), 487.
— (Troohalopteron), 487.
— (Zosterops), 435.
oxyacanthae (Meganephira), 44, 55.
— (Phalaena), 55.
oxybiensis (Bryophila), 3.
pacificus (Histiionicus), 145.
Pachycare, 444.
Pachycephala, 444-9.
Pachylia, 336, 337, 343, 387, 388.
pachyrhyncba (Pentbolaca), 472.
Pachysylvia, 456.
Pachyuromys, 313, 314.
paena (Erythropygia), 472.
Pagarnea, 349.
palawana (Callisitta), 440.
— (Sitta), 440.
palirrhoea (Aniaodes), 305.
— (Perixera), 305.
pallasii (Cinclus), 504.
pallens (Butalis), 153.
pallescens (Troglodytes), 153.
pallida (Acronycta), 7.
— (Bryophila), 5.
— (Perigonia), 400.
pallidiceps (Rhipidura), 497.
pallidior (Bradypterus), 469.
— (Calamonastes), 465.
— (Metopoceras), 49.
pallidipeetus (Dendrobiastes), 492.
— (Muscicapula), 492.
pallidipes (Horeites), 458.
pallidus (Buteo), 149.
— (Telophonus), 449.
Palluperina, 44.
palmeri (Amplypterus), 372.
— (Phaeornis), 477.
palniensis (Ptychopoda), 311.
Palpangula, 96.
palpebrosa (Zosterops), 435.
palumbus (Columba), 231.
palustris (AcrocephaluB), 189.
— (Parus), 185, 443.
pan (Hemeroplanes), 395.
panaceorum (Acrobyla), 98.
— (Armada), 98
panayensis (Eumyias), 490, 491.
— (Stoparola), 490, 491.
pancratii (Britbys), 15.
— (Noctua), 15.
Pandesma, 93.
Pandion, 150, 207.
Panurus, 186.
paphus (Protoparce), 364.
Papilio, 343.
535
papuana (Myiagra), 500.
— (Microeca), 490.
papuense (Dicaeum), 328.
papuensis (Pipra), 328.
par (Pachycephala), 444, 445.
paradela (Scopula), 294.
paradelpharia (Scopula), 297.
Paradieaea, 331.
paradisaea (Sterna), 131, 244.
paradisi (Tchitrea), 499.
paradoxus (Syrrhaptes), 232.
Parallelia, 107.
parambanus (Turdus), 475.
Parascotia, 110.
parasiticus (Stercorarius), 135.
Parastichtis, 42, 59, 112.
paratropa (Anisodes), 302.
parce (Hemeroplanes), 395.
Parisoma, 495.
Parmoptila, 432.
Parus, 158, 184, 185, 442-4.
parva (Eublemma), 79.
— (Muscicapa), 153.
— (Noctua), 79.
— (Porzana), 248.
— (Siphia), 153.
parvimacula (Anumeta), 96.
parvirostris (Artamus), 455.
— (Phylloscopus), 462.
parvulus (Mimus), 478.
Pastor, 175, 180.
paupercula (Polyptychus), 159.
pauli (Cleophana), 66.
— (Omphalophana), 66.
pealei (Falco), 149.
Pechipago, 113, 114.
pectinicornis (Cleophana), 67.
peotoralia (Calliope), 474.
— (Crateroscelis), 482.
— (Luscinia), 474.
— (Pachycephala), 448, 449.
— (Rhinomyias), 499.
pekinensis (Alauda), 151.
pelagicus (Haliaetus), 150.
— (Hydrobates), 223.
— (Phalacrocorax), 147.
Pelecanus, 332.
pellicida (Momonipta), 508.
Pelicinius, 450, 451.
pelios (Turdus), 476. •
peltigera (Chloridea), 72.
pendulinus (Anthoscopus), 441.
— (Remiz), 441.
penelope (Anas), 143, 214.
peninsulae (Pachycephala). 440.
penricei (Scopula), 282.
Pentholaea, 472.
Penthornis, 444.
perbrunneata (Hamalia), 309.
Perdix, 251.
perdix (Brachyrhamphus), 130.
— (Perdix), 251.
peregrina (Hadena), 111.
— (Miselia), 111.
peregrinus (Falco), 149, 200.
perfilata (Scopula), 293.
Pericyma, 93.
Perigonia, 400.
periophthalmica (Callaeops), 498.
— (Tchitrea), 498.
periplecta (Zosterops), 434.
Perixera, 278, 279, 304, 305.
permixta (Eublemma), 78.
— (Thalpochares), 78.
Pernis, 206.
pernivea (Eublemma), 84.
peromissa (Cyornis), 491, 492.
peronii (Turdus), 476.
perplexa (Protoparce), 365.
perpulla (Cisticola), 466.
perpulverosa (Lipotaxia), 270.
persimilis (Anthoscopus), 441.
— (Athetis), 111.
— (Remiz), 441.
personatus (Artamus), 455.
perspicillata (Oidemia), 146.
perspicillatus (Phalacrocorax), 148.
pertinax (Athetis), 16.
petrea (Bryophila), 2.
Phaeochlaena, 508.
phaeopus (Numenius), 140, 241.
Phaeornis, 477.
Phalacrocorax, 147, 148, 221, 222.
Phalaena, 5, 7, 11, 12, 19, 27-62, 94, 95.
Phalaropus, 140, 239, 240.
Phaleris, 131.
phanus (Pelicinius), 451.
Phasianus, 251.
Philentoma, 499.
philippina (Lucanitis), 98.
— (Syneda), 98.
philippinensis (Cyornis), 492.
philippinus (Phyllergates), 468.
Philomachus, 140, 235.
philomelos (Turdus), 191, 477.
Phlogophora, 55, 87.
phoebei (Turdinus), 484.
phoeus (Artamus), 455.
phoeniceum (Trochalopteron), 487.
Phoenicurus, 193, 194, 474.
phoenicurus (Phoenicurus), 193.
Pholus, 347, 403-6.
phorbas (Pholus), 406.
photophila (Agrotis), 32.
— (Lycophotia), 32.
phylarcha (Comostolopsia), 267.
-■S3*;
Phyllergates. 467, 468.
phyllis (Platysphinx), 165.
Phyllophila, 77, 78.
Phylloscopus, 154, 188, 461-3.
Physopterus. 262.
Phytometra. 115.
piabilis (Platysphinx), 165.
Pica, 174.
pica (Pica), 174.
picata (Agrotis), 111.
picturata (Cleophana). 71.
— (Metapistis), 71.
Picus, 197.
pierretii (Episema), 22.
— (Euxoa), 22.
— (Heliophobus), 22.
pilaris (Turdus), 190.
pileata (Pyrrhula), 178.
pilibrachia (Anisodes), 278.
pinaiae Oreozosterops), 437.
Pinarochroa, 471.
Pinarolestes, 453.
Pinicola, 157.
Pipistrellus, 316.
Pipra, 328, 331.
Pisoraca, 271-6, 301.
pistacina (Phalaena), 38.
Pitohui, 453, 454.
placens (Climacteris), 439.
planorum (Parus), 443.
plataea (Trochiodes), 508.
Platalea, 138.
plateni (Hyloterpe), 446.
— (Pachycephala), 446.
— (Prionochilus), 430, 431.
platensis (Oistothorus), 505.
platyptera (Calophasia), 71.
— (Noctua), 71.
platyrhyiicha (Anas), 142. 212.
Platysphinx, 163-5.
Platysteira, 496.
plebeius (Crateropus), 486.
Plectrophenax, 155, 181.
Plegadis, 208.
plionocentra (Pylarge), 280.
— (Scopula), 280.
Plotus, 247.
Pluaia, 87.
pluto (Madoryx), 394.
— (Xylophanes), 408.
pluvius (Picus), 197.
Podiceps, 129, 224, 225-9.
Poecilictis, 316.
Poecilodryaa, 444, 494, 495.
poeciloptera (Anisodes), 301.
— (Pisoraca), 301.
polemia (Microloxia), 300.
Polia, 43, 47-9, 52-4, 112.
poliocephalus (Malaconotus). 452.
poliogastra (Zosterops), 432.
poliogyna (Brachypteryx), 479.
pollicaris (Rissa), 134.
polybela (Euxoa), 23.
— (Omphaloscelis), 23.
Polydesma, 93.
polygramma (Anthophila), 78.
— (Eublemma), 78.
Polyphaenis, 56.
Polypoetes, 509.
Polyptychus, 159, 160, 167.
Polysticta, 145.
polyterpes (Scopula), 283.
Pomarea, 503.
pomarinus (Stercorarius), 135, 247.
Pomatorhinus, 488.
pontica (Acronycta), 7.
— (Craniophora), 7.
porcus (Xylophanes), 349, 409.
Porzana, 248.
porzana (Porzana), 248.
powelli (Agrotis), 31.
— (Catocala), 99.
— (Euxoa), 31.
— (Morinonia), 99.
praecipuina (Agrotis), 37.
— (EpipsUia), 37.
praeruptorum (Scopula), 293.
praesignipuncta (Scopula), 284.
Prasinocyma, 267.
pratensis (Anthus), 152, 182.
Pratincola, 471, 472.
precisa (Metachrostis), 6.
— (Oederemia), 6.
prillwitzi (Arachnothera), 427.
— (Mixornis), 480.
princeps (Lanius), 452.
Prinia, 457.
prinioides (Cisticola), 465.
Prionochilus, 430, 431.
Prionops, 452.
Pristorhamphus, 431.
Procnias, 329, 330.
Procus, 46
Prodenia, 20.
Promerops, 328.
promissa (Catocala), 100.
Promotestra, 47.
pronoe (Enyo), 397.
pronuba (Agrotis), 35.
— (Phalaena), 35.
Proparus, 481.
propinquilinea (Neromia), 299.
Protarabulyx, 370-3.
protca (Eumichtis), 60.
— (Phalaena), 60.
proterocelis (Scopula), 291.
537
Prothymnia, 109.
Protomeceras, 89.
Protoparce, 336, 347, 364-9.
Proxenus, 112.
proxima (Gerygone), 494.
Prunella, 194, 503.
Pseudamathes, 6.
Pseudocalyptomena, 496.
pseudoderthisa (Luperina), 44.
pseudodoxa (Scopula), 297.
Pseudogerygone, 493.
Pseudohadena, 42, 43.
Pseudomecia, 116.
pseudoperla (Bryophila), 5.
pseudophema (Scopula), 285.
Pseudophia, 105, 106.
Pseudopseustris, 22.
Pseudosphinx, 334, 374.
pseudostrina (Eublemma), 80.
Pseudotharrhaleus, 484, 485.
Pseudozosterops, 437.
psi (Acronyctia), 7.
— (Plialaena), 7.
psittacula (Phaleris), 131.
Psittacus, 331.
Pteruthius, 478.
Ptilooichla, 482.
Ptilopyga, 482.
ptilosous (Macronua), 480.
Ptochophyle, 270.
Ptychopoda, 310, 311.
Ptyrticus, 483.
puella (Hypothymis), 496.
puerpera (Catocala), 101.
Puffinus, 135, 223.
pugnax (Philomaehus), 140, 235.
pulchra (Camaroptera), 459.
pulverata (Hadula), 43.
— (Mamestra), 43.
punctosa (Cirphis), 10.
— (Simyra), 10.
purpurina (Eublemma), 86.
purpurina (Phalaena), 86.
pusilla (Aethia), 131.
— (Sericorms), 461.
pusillus (Simorhynchus), 131.
putrescens (Cirphis), 10.
— (Noetua), 10.
pygargus (Circus), 204.
pygmaea (Aethia), 131.
— (Muscicapa), 329.
— (Myrmotherula), 329.
pygmaeus (.Simorhynchus), 131.
pygmea (Platalea), 138.
pygmeus (Eurynorhynchus), 138.
Pylarge, 280.
Pyralis, 73, 86, 113.
pyramidea (Amphipyra), 89.
pyramidea (Phalaena), 89.
pyrenaica (Certhia), 438.
— (Motacilla), 331.
Pyrenaicis, 331.
pyrenaicus (Aegithalos), 442.
Pyrois, 89.
pyrrhoptera (Malacocincla), 483.
pyrrhopterum (Philentoma), 499.
pyrrhopterus (Turdinus), 483.
Pyrrhula, 157, 178.
pyrrhula (Pyrrhula), 157, 178.
quadrivirgata (Erythropygia), 472.
quadrivirgula (Epimecia), 64.
— (Hypomecia), 64.
quarta (Erolia), 137.
fiuerquedula (Anas), 142, 213.
quoyi (Cracticus), 455.
Rabinopteryx, 64.
raddei (Gallinago), 136.
— (Scolopax), 136.
radius (Bombyx), 32.
— (Euxoa), 32, 33.
Rallus, 249.
ramsayi (Zosterops), 433.
Raphia, 98.
Rattus, 319.
ravula (Bryophila), 5.
— (Noetua), 5.
rayi (Motacilla), 183.
rebecca (Antitype), 53.
receptricula (Bryophila), 5.
reclusus (Macronus), 480.
reconditaria (Aecidalia), 298.
rectisecta (Scopula), 291.
regina (Cosmia), 41.
— (Enargia), 41.
Regulus, 185, 441.
regulus (Aesalon), 149.
— (Regulus), 185, 441.
reichenowi (Burnesia), 457.
— (Chlorophoneus), 451.
— (Cinnyris), 425.
— ■ (Dioptrornis), 489.
— (Erythropygia), 472.
— (Muscicapa), 489.
— (Pachycephala), 447.
— (Prinia), 457.
Remiz, 441.
rendovae (Zosterops), 436.
restituta (Perigonia), 400.
resumens (Pachylia), 388.
rcussi (Polyptychus), 160.
reutlinger (Temnora), 512.
revayana (Sarrothripus), 114.
538
revayana (Tortrix), 114.
Rhampliocharis, 431.
Klicctes, 453.
Rhinomyias, 499.
Rhipidura, 496-8.
Rhizotype, 55.
Rhodocleptria, 72.
Rhodophoneus, 450, 451.
Rhodostethia, 134.
Rhodostrophia, 268.
Rhopoterpe, 328.
ribbei (Pomarea), 503.
ricketti (Phylloscopus), 462.
ridgwayi (Lagopus), 148.
ridibundus (Larus), 133, -11.
riggenbachi (Oenanthe), 471.
— (Saxicola), 471.
Riparia, 154, 196.
riparia (Cerphis), 12.
— (Clivicola), 154.
— (Leucania), 12.
— (Riparia), 154, 196.
ripponi (Prunella), 503.
Risaa, 134, 246.
Rivula, 110.
roberti (Cossypha), 473.
— (Turdinulus), 482.
robiginosa (Agrotis), 31.
— (Euxoa), 31.
roboris (Eumichtis), 60.
— (Hadena), 60.
robusta (Cisticola), 466.
rodgersii (Fulmarus), 135.
romae (Dicaeum), 429.
rosacea (Cortyta), 93.
— (Scotogramma), 56.
rosae (Nephele), 512.
rosea (Antitype), 53.
— (Autophila), 92.
— (Catocala), 101.
— (Rhodostethia), 134.
roseata (Spintherops), 91.
roseonitens (Mamestra), 43.
— (Pseudohadena), 43.
roseus (Aegithalos), 185.
— (Pastor), 175.
rosinans (Bryophila), 5.
rosinata (Polia), 53.
rosseli (Dicaeum), 429.
rosseliana (Gerygone), 493, 494.
— (Pachycephala), 448.
rosselianus (Monarcha), 502.
rossonim (Pratincola), 471.
— (Saxicola), 471.
rothschildi (Anthoscopus), 442.
— (Arachnothera), 428.
— (Camaroptera), 459.
— (Laniarius), 450.
rothschildi (Poecilictis), 316.
rotroui (Dasysternum), 45.
— (Euxoa), 29.
rubecula (Erithacus), 194, 474.
— (Myiagra), 500.
rubella (Luperina), 44.
rubetra (Saxicola), 193.
rubicunda (Lipotaxia), 269.
rubiginosus (Crateropus), 486.
— (Laniarius), 451.
— (Pelicinius), 451.
rudis (Anisodes), 305.
rudolfi (Chlorophoneus), 451.
— (Laniarius), 451.
rufa (Alectoris), 251.
— (Cisticola), 467.
— (Drymoica), 467.
rufescentior (Amathes), 41.
— (Cossypha), 473.
— (Proparus), 481.
ruficeps (Cisticola), 465.
— (Larvivora), 474.
— (Luscinia), 474.
— (Stachyridopsis), 480.
ruficollis (Erolia), 138.
— (Myiagra), 500.
— (Podiceps), 229.
rulicrissa (Rhinomyias), 499.
rutifrons (Cj'ornis), 492.
— (Rhipidura), 496, 497.
— (Stachyridopsis), 480.
rufigastra (Cyornis), 491.
rufigula (Myiagra), 500.
rufina (Netta), 215.
— (Phalaena), 39.
rufinucha (Pachycephala), 445.
rufitergum (Garrulus), 175.
rufiventris (Rhipidura), 497.
rufobrunnea (Craterosceles), 482
rufocinctus (Lioptilus), 483.
rufocinerea (Monticola), 475.
rufofuscus (Harpolestes), 450.
— (Telophonus), 450.
rufogularis (Ianthocincla), 488.
— (Proparus), 481.
rufostigmata (Athetis), 17.
rufus (Bathmocercus), 483.
— (Neocossyphus), 473.
rugifrons (Agrotis), 24.
— (Euxoa), 24.
ruki (Tephras), 438.
rumicis (Acronycta), 7.
rupestris (Lagopus), 14s.
rupicola (Sitta), 440.
rustica (Emberiza), 155.
— (Hirundo), 154, 195.
— (Protoparce), 367.
rusticola (Scolopax), 243.
539
rustieolus (Falco), 148.
ruticilla (Amathes), 38.
— (Nootua), 38.
sabinii (Xeraa), 134.
sabourodi (Anydrophila), 97.
— (Palpangula), 97.
sabulosa (Anurneta), 95.
— (Azenia), 86.
— (Eublemma), 86.
Sagittarius, 328.
sagra (Eupyrrhoglossum), 400.
sahariensis (Antitype), 53.
saipanensis (Rhipidura), 497.
sakaiorum (Abrornis), 502.
sakhalina (Erolia), 138.
saleyerensis (Cinnyris), 427.
salmonea (Jugurthia), 6.
— (Polia), 53.
Salpornis, 439.
salvadorii (Pachycephala), 447.
— (Poecilodryas), 494.
sana (Cerocala), 108, 109.
sancta (Clytie), 106.
— (Pseudophia), 106.
sanctiflorentis (Antarchaea), 109.
sandvicensis (Sterna), 243.
santolinae (Cucullia), 63,
saphes (Scopula), 295.
sapsworthi (Cinclus), 504.
Saragossa, 43.
sarawacensis (Parus), 442.
sardus (Cinclus), 504.
Sarrothripus, 114.
satellitia (Pholus), 403.
saturata (Pachysylvia), 456.
saturatior (Cossypha), 473.
— (Sitta), 440.
saturatus (Eupetes), 488.
— (Machaerirhynchus), 501.
Saurothera, 330.
Saxicola, 193, 470-2.
seandens (Loxia), 331.
scapulosa (Cerocala), 108, 109.
Scelolophia, 307.
schisticeps (Pomatorhinus), 488.
schistisagus (Larus), 132.
schistocercus (Abbotornis), 454.
schistochlamys (Garrulax), 487.
schlegeli (Pachycephala), 447.
schoana (Pinarochroa), 471.
— (Zosterops), 433.
schoeniclus (Emberiza), 181.
schoenobaenus (Acrocephalus), 190.
schraderi (Cisticola), 466.
schwaneri (Abrornis), 502.
scillae (Heliophobus), 22.
scillae (Leucochlaena), 22.
scirpaeeus (Acrocephalus). 189.
scitula (Erastrina), 76.
— (Eublemma), 76.
sciurorum (Myiagra), 500.
sclateri (Monticola), 475.
Scoliopteryx, 89.
Scolopax, 136, 243.
Scotogramma, 51, 56, 57.
scotoptera (Athetis), 19.
— (Caradrina), 19.
scops (Asio), 200.
Scopula, 280-98, 307, 308.
scouleri (Microcichla), 474.
scrophulariphaga (Cucullia), 62.
scrophulariphila (Cucullia), 62.
scutosa (Melicleptria), 73.
— (Phalaena), 73.
scyron (Isognathus), 343, 349, 382.
sebdouensis (Conistra), 40.
— (Orrhodia), 40.
secalis (Phalaena), 46.
— (Trachea), 46.
secedens (Hyloterpe), 447.
— (Pachycephala), 447.
seebohmi (Bradypterus), 469.
— (Lusciniola), 469.
— (Oenanthe), 471.
— (Saxicola), 471.
sceboldi (Saragossa), 43.
segetum (Anser), 141.
— (Euxoa), 28.
— (Phalaena), 28.
seheriae (Aethopyga), 425.
sejuncta (Culicicapa), 500.
Semaeopus, 269.
semibrunnea (Lithophanc), 61.
— (Noctua), 61.
semicinctus (Dioptrornis), 489.
— (Muscicapa), 489.
semicostalis (Elachyophthalma), 323.
semirufa (Cossypha), 473.
semperi (Zosterops), 435.
senegalensis (Cinnyris), 426.
— (Zosterops), 432, 433.
senegalus (Harpolestes), 449, 450.
— (Telophonus), 449, 450.
sennaarensis (Pandesma), 93.
senniger (Polyptychus), 159, 160.
sepiaria (Malacocincla), 484.
septentrionalis (Rhipidura), 498.
sequens (Gerygone), 494.
seranensis (Myiagra), 500.
— (Zosterops), 434, 435.
serena (Miselia), 48.
— (Phalaena), 48.
— (Scopula), 296.
sericealis (Rivula), 110.
540
Sericornis, 461.
serrate (Omphiilopliana), 66.
serrator (Mergus), 147, 221.
serrirostris (Anser), 141.
Scrpentarius, 328.
serpentarius (Falco), 328.
Sesamia, 12.
sesamiodes (Borolia), 116.
Sesia, 400, 401.
Setaria, 482.
setosa (Rhipidura), 497.
sexfilis (Paradisaea), 331.
sexta (Protoparcc), 336, 347, 364.
sharpei (Anthoscopus), 441.
— (Pachycephala), 448.
sharpii (Argya), 486.
— (Crateropus), 486.
sibilatrix (Phylloscopus), 188, 463.
sibiricus (Larus), 133.
sicula (Cirphis), 9.
— (Leucania), 9.
Sidemia, 38, 44, 45.
Sideridis, 9, 11.
Sigmodus, 452.
silene (Conistra), 40.
silene (Phalaena), 40.
silenes (Epia), 47.
— (Noctua), 47.
silenides (Mamestra), 47.
— (Promotestra), 47.
silens (Arremon), 328.
— (Tanagra), 328.
simillima (Motacilla), 152.
Simorhynchus, 131.
simplex (Cyornis), 492.
simplicilinea (Semaeopus), 269.
simplicissiraa (Cisticola), 467.
simulatricula (Bryophila), 3. 4.
simulatrix (Epipsilia), 31.
— (Noctua), 31.
Simyra, 7, 8, 10.
sinae (Phoenicurus), 474.
siparaja (Aethopyga), 42f>.
Siphia, 153, 491, 492.
Sitta, 184, 329, 439, 440.
Siva, 479.
smithi (Crateropus), 486.
— (Zosterops), 432.
Smithornis, 496.
sobatensis (Cisticola), 466.
socotrana (Zosterops), 432.
sodae (Scotogramma), 56,
softa (Miselia), 110.
Solaris (Cinnyris), 427.
solieri (Eumichtis), 58.
— (Hadena), 58, 59.
solitaria (Gallinago), 137.
solitarius (Monticola), 475.
sollicitans (Dicaeum), 430.
Somateria, 146.
somereni (Cossypha), 473.
sopbiae (Leptopoecile), 441.
sophorae (Brassolis), 343.
sordida (Pinarochroa), 471.
souinianga (Cinnyris), 428.
spaldingi (Cracticus), 455.
Spatula, 143, 214.
spatzi (Anumeta), 95.
spectabilis (Somateria), 146.
spectrum (Apopestes), 90.
spermologus (Coloeus), 174.
spilonota (Salpornis), 439.
spinifera (Euxoa), 26.
— (Noctua), 26.
spinoletta (Anthus), 152.
spinosa (Hadena), 112.
— (Parastichtis), 112.
Spintherops, 91, 92.
spinus (Carduelis), 176.
Spodoptera, 15.
sponsa (Catocala), 99.
— (Mormonia), 99.
squamatus (Mergus), 147.
squamiceps (Chloroeharis), 437.
— (Pseudozosterops), 437.
-Squatarola, 136, 235.
squatarola (Squatarola), 136, 235.
stabilis (Monima), 38.
— (Phalaena), 38.
Stacbyridopsis, 480.
Stachyris, 480, 481.
stagnatilis (Tringa), 238.
standfussi (Parastichtis), 59.
Staphidia, 479.
Stasiasticus, 469.
Steatomys, 318.
stejnegeri (Anthus). 151.
— (Oidemia), 146.
stellaris (Botaurus), 209.
stellatus (Colymbus), 130, 230.
stelleri (Polysticta), 145.
Stercorarius, 135, 247.
Sterna, 131, 132, 243, 244.
Stibarostoma, 278.
stigmatica (Calophasia), 71.
— (Platysphinx), 165.
stigmatilinea (Anisodes), 278.
Stilbia, 14, 15.
stillata (Comostolopsis), 267.
stolida (Grammodes), 107.
— (Noctua), 107.
Stoparola, 490, 491.
straminea (Anumeta,) 97.
— • (Epipsilia), 42.
— (Euxoa), 42.
straminea (Palgangula), 97.
541
strepera (Anas), 142, 212.
Streptopelia, 232.
striata (Ai'gyrospila), 13.
— (Muscicapa), 187, 489.
— (Neositta), 440.
— (Sesamia), 13.
— (Upupa), 328.
striatus (Falcinellus), 328.
— (Oriolus), 331.
strigilis (Protambulyx), 371.
strigula (Siva), 479.
Strix, 150, 200.
Sturnus, 175.
suava (Eublemma), 85.
— (Noctua), 85.
subapicalis (Temnora), 512.
subaurantia (Pachycare), 444.
subbuteo (Falco), 201.
subcristatus (Lophozosterops), 438.
subcyanea (Poecilodryas), 494.
subfervens (Ptyehopoda), 311.
sublutescens (Scopula), 292.
subminuta (Erolia), 138.
subperla (Cataraecia), 6.
subplumbeola (Jugurthia), 6.
— (Oedibrya), 6.
subpulchellata (Scopula), 286.
subruficapilla (Cisticola), 466.
subterminalis (Eublemma), 82.
subtilis (Epimecia), 64.
— (Rabinopteryx), 64.
subvenata (Eublemma), 80.
— (Thalpochares), 80.
subvenusta (Antitype), 52.
suffusa (Agrotis), 27.
— (Phalaena), 27.
Sula, 222.
sulphuralis (Emmelia), 74.
sultana (Catoeala), 100.
sumatranus (Phyllergates), 467.
sumbavensis (Zosterops), 433, 434.
sumbensis (Rhipidura), 496.
auperbior (Ephialtias), 509.
superciliaris (Abrornis), 502.
— (Camaroptera), 459.
— (Oreozosterops), 437.
— (Zosterops), 437.
superciliosa (Zosterops), 433.
superciliosus (Artamus), 455.
supertiua (Rhipidura), 497.
supina (Scopula), 281.
suratensis (Streptopelia), 232.
Suya, 458.
swainsoni (Isognathus), 378.
swinhoei (Stachyris), 480.
syces (Pachylia), 337, 343, 387.
sylvatica (Strix), 200.
Sylvia, 190, 463, 493.
sylviella (Anthoscopus), 441.
Sylvietta, 460.
symmixta (Hypothymis), 496.
Syneda, 98.
Synthliborhamphus, 131.
Synthymia, 86.
sypharioides (Anisodes), 272.
— (Pisoraca), 272.
syrdaja (Clytie), 106.
Syrrhaptes, 232.
syrtana (Copicucullia), 63.
syrtensis (Eublemma), 85.
szetschuanus (Troglodytes), 504.
tachycrypta (Colluricincla), 453.
taciturna (Tanagra), 328.
taciturnus (Arremon), 328.
Tadorna, 211.
tadorna (Tadorna), 211.
taedium (Epistor), 399.
Taeniocampa, 22.
tagulana (Gerygone), 494.
tahanensis (Pteruthius), 478.
taivanus (Troglodytes), 504.
Tanagra, 328, 331.
Tanaostyla, 508.
Tapinostola, 14.
Tarache, 74, 75.
tardinata (Malacocinela), 484.
Tarsiger, 154, 473.
Tatare, 464.
Taterillus, 317.
Tathorhynchus, 92.
Tchitrea, 498, 499.
telephonus (Cuculus), 150.
tellieri (Pseudopseustris), 22.
— (Taeniocampa), 22.
Telophonus, 449, 450.
temminckii (Erolia), 138, 237.
Temnora, 160, 161, 512.
tenebrosa (Pachycephala), 445.
tenebrosus (Crateropus), 486.
tenuirostris (Erolia), 138.
— (Pufiinus), 135.
tenuis (Eumegethes), 80.
— (Thalpochares), 80.
tepa (Pachycephala), 448.
Tephras, 438.
tephrocotis (Montifringilla), 156.
tephronota (Sitta), 440.
tephrus (Hipposideros), 315.
ternatanus (Zosterops), 434, 435.
terraesanctae (Parus), 443.
tersa (Xylophanes), 349, 413.
tessacourbe (Muscicapa), 444.
— (Penthomis), 444.
542
testacea (Apamea), 43.
tetra (Amphipyra), 90.
— (Noctua), 90.
Tetrao, 250.
tetrio (Pseudosphinx), 334, 374.
tetrix (Lyrurus), 250.
textilis (Amytornis), 456.
thagus (Pelecanus), 332.
Thalpochares, 78-80, 83.
Thalpophila. 45.
thapsiphaga (Cucullia), 61.
Thirmida, 509.
thoas (Papilio), 343.
thoracicus (Hylophilus), 456.
Thryothorus, 505.
thyelia (Xylophanes), 415.
tiandu (Rhipidura), 497.
tianduana (Pachycephala), 445.
tiansehanica (Certhia), 439.
tibetanus (Parus), 443.
tibicen (Gymnorhina), 454.
tickelli (Pomatorhinus), 488.
Timora, 13.
tinniens (Cisticola), 466.
tinnunculus (Faleo), 202.
tirhaca (Anua), 105.
— (Phalaena), 105.
titan (Sesia), 402.
Tithraustes, 508, 509.
tobagensis (Mimus), 477.
Todopsis, 457, 483.
toni (Sylvia), 463.
tonkinensis (Aethopyga), 425.
torquata (Pratincola), 472.
torquatus (Formicarius), 328.
— (Saxicola), 193, 472.
— (Turdus), 192.
torquilla (Jynx), 198.
Tortrix, 114, 115.
toruensis (Dioptrornis), 489.
— (Muscicapa), 489.
Totanus, 139.
totanus (Tringa), 238.
townsendi (Plectropbenax), 156.
trabealis (Erastria), 74.
— (Pbalaena), 74.
Tracbea, 46.
tragopoginis (AmpbipyTa), 90.
transcaspicus (Monticola), 475.
transcaucasica (Rhodostrophia), 268.
translucida (Dyspbania), 265.
traversi (Miro), 494.
Tregellasia, 495.
tribeles (Anisodes), 276.
tricolor (Elacbyopbtbalraa), .'!L'4.
tridactyla (Rissa), 134, 246.
tridactylus (Loxia), 330.
— (Melanobucco). 330.
tridens (Acronycta), 7.
— (Noctua), 7.
trifolii (Scotogranima), 56.
Trigonopbora, 55.
trigonostigma (Dicaeum). 430.
trirnacula (Bombyx), 21.
— (Derthisa), 21.
Tringa, 137, 139, 237-9.
tripartita (Abrostola). 115.
— (Pbalaena), 115.
Tiiphaena, 34, 35.
triplasia (Abrostola), 1 15.
triptolemus (Leucorbampha), 391.
trisagittata (Polia), 47.
tritici (Euxoa), 30.
— (Phalaena), 30.
trivialis (Anthus), 152, 182.
trivirgatus (Phylloscopus), 462.
trobriandi (Pacbycepbala), 444.
Trocbatopteron, 487, 488.
trocbiloides (Acanthopneuste), 462.
— (Phylloscopus), 462.
trochilus (Phylloscopus), 188.
Trochiodes, 508.
Troglodytes, 153, 195, 504.
troglodytes (Troglodytes), 153, 504.
troille (Uria), 247.
tropicalis (Protoparce), 364.
trux (Euxoa), 28.
— (Noctua), 28.
Trygodes, 270.
tucumanus (Cistothorus), 505.
tudjuensis (Zosteropa), 434.
tumiditibia (Scopula), 298.
tunneyi (Cracticus), 455.
turatii (Stilbia), 15.
turbata (Xylophanes), 162.
turbatrix (Dyspbania), 265.
Turdinulus, 481, 482.
Turdinus, 483, 484, 485.
turdinus (Ptyrticus), 483.
turdoides (Cataponera), 487.
Turdus, 154, 190-2, 475-7.'
turneri (Anisodes), 278.
— (Stibarostorna), 278.
turtur (Streptopelia), 232.
tscbitscherini (Sitta), 440.
typica (Terra), 148.
Tyrannus, 329.
tytleri (Hirundo), 154.
Tyto, 200.
ugandae (Macrosplienus), 484.
— (Turdinus), 484.
ulicis (Cosmia), 41.
— (Enargia), 41.
Ulochlacna, 20.
543
ultramnntana (Certhia), 439.
umbratilis (Rhinomyias), 499.
undata (Sylvia), 463.
unica (Zosterops), 434.
unicolor (Pseudotharrhaleus), 485.
uniforniis (Catephia), 94.
— (Mageutica), 94.
unigravis (Lobocleta), 310.
unipuncta (Cirphis), 12.
— (Noctua), 12.
Upupa, 196, 328.
uralensis (Falco), 148.
urbana (Agrotis), 24.
urbica (Delicbon), 195.
Uria, 130, 247.
urile (Phalacroeorax), 148.
urogallus (Tetrao), 250.
Urolais, 461.
vaccinii (Conistra), 40.
vae (Felovia), 507.
valentini (Cryptolopha), 501.
Valeria, 54.
vali (Ctenodactylus), 507.
vallantini (Catocala), 102, 104.
Vanellus, 235.
vanellus (Vanellus), 235.
variabilis (Emberiza), 155.
variegata (Ampelis), 329.
— (Amphipyra). 89.
— (Mamestra), 58.
— (Miselia), 58.
variegatus (Numenius), 140.
— (Procnias), 329.
vaulogeri (Cleophana), 67.
vegae (Larus), 132.
vegeta (Zosterops), 433.
vellalavella (Zosterops), 436.
velox (Eublemma), 78.
— (Noctua), 78.
ventralis (Cylindroides), 264.
venusta (Polia), 52.
venustus (Artamus), 455.
verbasci (Cucullia), 61.
— (Phalaena), 61.
veronicae (Conistra), 40.
— (Noctua), 40.
versicolor (Cleophana), 70.
versteri (Pristorhamphus), 431.
vespertalis (Aegle), 73.
— (Pyralia), 73.
vespertinus (Falco), 202.
vestalis (Protoparce), 369.
vestigialis (Euxoa), 26.
— (Noctua), 26.
viator (Anisodes), 277.
vicaria (Platysphinx), 164.
vicaria (Poecilodryas), 494.
viminalis (Bombycia), 54.
virens (Zosterops), 433.
Vireo, 455.
Vireolanius, 456.
virescens (Gerygone), 493.
— (Pseudogerygone), 493.
— (Sylvia), 493.
virginalis (Anthophila), 82.
viridaria (Antarchaea), 109.
— (Phalaena), 109.
viridiflava (Microeca), 490.
viridigularis (Colymbus), 130.
— (Gavia), 130.
viridis (Androphilus), 485.
— (Picus), 197.
viriginalis (Eublemma), 82.
viscivorus (Turdus), 191.
viscosa (Hadjina), 76.
— (Mythimna), 76.
vitalba (Noctua), 45.
— (Thalpophila), 45.
vitellina (Noctua), 11.
— (Sideridis), 11.
vitis (Pholus), 347, 405.
vittata (Graueria), 484.
vivida (Catocala), 101.
volloni (Amathes), 6.
— (Pseudamathes), 6.
vulcani (Zosterops), 436.
vulcanorum (Cinnyris), 426.
vulgaris (Coceothraustes), 157.
— (Sturnus), 175.
vulpinus (Bathmocercus), 483.
vuteria (Phalaena), 12.
— (Sesamia), 12.
waigiuensis (Cryptolopha), 493.
walkeri (Amphimoea), 363.
warionis (Amephana), 65, 66.
— (Cleophana), 65.
waterstradti (Cryptolopha), 462.
— (Phylloscopus), 462.
— (Suya), 458.
westernensis (Zosterops), 433.
wetterensis (Pachycephala), 446.
whiteheadi (Erythrocichla), 482.
— (Hyloterpe), 446.
— (Zosterops), 436.
wichkami (Larvivora), 474.
— (Luscinia), 474.
wiglesworthi (Anthreptes), 428.
witherbyi (Erithacus), 474.
witzenmanni (Amathes), 37.
— (Orthosia), 37.
wolfi (Xylophanes), 414.
wollastoni (Eublemma), 84.
544
woodhousei (Parmoptila), 432.
woodward! (Amytornis), 456.
— (Colluricincla), 453.
Xylocarnpa, 60.
Xylophanea, 162, 348, 349, 408-15.
xanthenea (Hydroecia), 42.
— (Jortyna), 42.
Xanthia, 40.
Xanthodes, 73.
xanthographa (Agrotis), 36.
— (Phalaena), 36.
Xantholeuca, 40.
xantboleuca (Herpornia), 478.
xanthopygia (Cryptolopha), 501.
xanthopygius (Prionochilus), 430, 431.
Xema, 134.
Xenocopaychua, 473.
Xenorma, 508, 509.
xenoaceles (Lobocleta), 309.
Xenoaphingia, 168, 169, 512.
Xylina, 72.
Xylinadea, 263.
yakushimenaia (Merula), 476.
— (Turdua), 476.
ypsilon (Amplypterua), 372.
— (Noctua), 27.
Zanclognatha, 113.
Zanthopygia, 490.
zarudnyi (Aorooephalua), 464.
zeae (Cirphia), 12.
— (Noctua), 12.
zenobia(Cinnyria), 427.
Zethea, 110.
zeuctospila (Aniaodea), 274,
— (Piaoraca), 274.
zeylonua (Peliciniu8), 451.
Zosteropa, 432-7.
zuluenaia (Calamocichla), 464/
Printed In Htuellt Wat&on .( Vinry, /d., Lundun and Ayleibury.
LEPIDOPTERA
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A REVISION OF THE LEPIDOPTEROUS FAMILY
SPHINGIDAE
By the Hon. WALTER ROTHSCHILD, Ph.D.,
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