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THE ANNALS
AND
MAGAZINE OF NATURAL HISTORY,
INCLUDING
ZOOLOGY, BOTANY, ann GEOLOGY.
(BEING A CONTINUATION OF THE ‘ANNALS’ COMBINED WITIT LOUDON AND
CHARLESWORTI’S ‘ MAGAZINE OF NATURAL I{STORY.’)
CONDUCTED BY
ALBERT C. L. G. GUNTHER, M.A., M.D., Ph.D., F.R.S.,
WILLIAM CARRUTHERS, F.R.S., F.L.S., F.G.S.,
AND
WILLIAM FRANCIS, F.1S.
eae
VOL. XIII.—SEVENTH SERIES.
\¥
% \
iN Ant
\
nON DO N:
PRINTED AND PUBLISHED BY TAYLOR AND FRANCIS.
SOLD BY SIMPKIN, MARSHALL, HAMILTON, KENT, AND CO., LD.;
BAILLIERE, PARIS: HODGES, FIGGIS, AND CO., DUBLIN :
AND ASHER, BERLIN,
1904,
“Omnes res creat sunt divine sapientise et potentix testes, divitix felicitatis
human :—ex harum usu Jonitas Creatoris; ex pulchritudine sapientia Domini ;
ex ceconomid in conseryatione, proportione, renovatione, potentia majestatis
elucet. Earum itaque indagatio ab hominibus sibi relictis semper sstimata ;
a veré eruditis et sapientibus semper exculta; malé doctis et barbaris semper
imimica fuit.””—Linnavs.
“Quel que soit le principe de la vie animale, il ne faut qu’ouvrir les yeux pour
voir qu’elle est le chef-d’ceuvre de la Toute-puissance, et le but auquel se rappor-
tent toutes ses opérations.”—Bruckner, Théorie du Systéme Animal, Leyden,
1767.
5 els faite leper Lhelsylvani powers
Obey our summons; from their deepest dells
The Dryads come, and throw their garlands wild
And odorous branches at our feet; the Nymphs
That press with nimble step the mountain-thyme
And purple heath-flower come not empty-handed,
But scatter round ten thousand forms minute
Of velvet moss or lichen, torn from rock
Or rifted oak or cavern deep: the Naiads too
Quit their loved native stream, from whose smooth face
They crop the lily, and each sedge and rush
That drinks the rippling tide: the frozen poles,
Where peril waits the bold adventurer’s tread,
The burning sands of Borneo and Cayenne,
All, all to us unlock their secret stores
And pay their cheerful tribute.
J. Taytor, Norwich, 1818,
ALERE § YFLAMMAM,
r
CONTENTS OF VOL, XIII.
[SEVENTH SERIES. ]
NUMBER LXXIII.
Page
I. The Prototheca of the Madreporaria, with Special Reference to
the Genera Calostylis, Linds., and Moseleya, Quelch. By Henry M.
enn, MOA Canutab., PbS. “(PlatetL). fis. 0. veces. sdieess 1
II. Some Parasitic Bees. By T. D. A. CocKERELL...........+ 33
II. Description of a new Genus of Frogs of the Family Dysco-
phide, and List of the Genera and Species of that Family. By
Eee BOGLENGEn, Pho ek mate: By sry ee ae eee oe 42
IV. The Collections of William John Burchell, D.C.L., in the
Hope Department, Oxford University Museum :—
I. Introduction. By Epwarp B. Poutron, D.Sc., M.A., F.R.S.,
SEs 0 (Plato TER ee A Se See aed Sele ea een 45
ITI. On a new Stridulating-organ in Scorpions discovered by W.
J. Burchell in Brazil in 1828. By R. I. Pocock, F.Z.S.
(ETAREPUV A) sabe che tras ise xe shale ® Siero ss «ere otra nye 56
V. Notes on Depastrum cyathiforme, Gosse. By E. 8. Russet.
“Elid, Vyas ARMAS elie pea ae ee ee eae 62
VI. On a new Genus of Spiders from Bounty Island, with Remarks
on a Species from New Zealand. By H. R. Hoae, M.A., F.Z.S. .. 65
VIL. On new Forms of Anomalurus and Sciwrus from Tropical
mere Ey, EV AROLD SCH WANN 05 fetes via cc'sia ss osc a ve 0 cea ai ele aie 70
VIII. On new Species of Lycenitde from Sierra Leone. By D.
BCE eth ore asia s rete kOe Ee ae ca en ine kale ede ve at ae 73
New Books :—Catalogue of the Collection of Birds’ Eggs in the
British Museum (Natural History). Vol. UI. By EKucenr W.
Oares and Capt. Savite G. Rem.—The Geological Structure
of Monzoni and Fassa. By Marie M. OcILvie Gorpon, D.Sc.,
MDs Hartt e Wali g ae 8 oe. vein Persie ahem nne 0 sels 76, 77
A Correction to “Notes on some Meduse from Japan,” by R.
Kirkpatrick, DAIS e cc ive ect neveaeee Poh Y One On ne 80
iv CONTENTS.
NUMBER LXXIV.
Page
IX. Notes on Mantide in the Collection of the British Museum
(Natural History), South Kensington, with Descriptions of new
Species, By W. EF. Kreey, F.:8., FBS. 6 o7eeeee amen ee Sore 2)!
X. The Collections of William John Burchell, D.C.L., in the Hope
Department, Oxford University Museum :—
III, Rhipidocérides et Malacodermes recueilles par W. J. Burchell
dans ses voyages en Afrique australe (1810-1815) et au
Brésil (1825-1830) ; avec la description de quatre espéces
nouvelles. Par J. BouRGEOIS
Se pre eee 89
XI, Rhynchotal Notes—XX. By W. L. DisTanr............ 108
XII. A Contribution to the Characteristic of Corals of the Group
Rugosa, By Prof. N. YAKOVLEFF ..... se eeeeee cece cece eceees 114
XIII. On the Distribution of Marine Animals. By Prof. M‘Inrosu,
M.D,, GAD SRS ie, +. Geet ieien wee kbs eel pata ts ee eee en LY
XIV. Descriptions of new Frogs and Snakes from Yunnan. By
GAG BOW NGAOR ES: ee. ois ao ste aut acee « giahele sie pie poy eect iolods 130
XV. On some Fishes from the Lakes of the Cameroon Mountain.
By Dr. Ernar LonnperG, C.M.ZS. Se. cece e cece eee ents 155
XVI. Descriptions of new Species of Lycenide from Borneo and
New Guinea. By Hamirton H. Druce, F.Z58., FES. ........ 140
> XVII. Two new Mammals from South America. By OLpDFIELD
BUETOMEAWS, oe coe fi tons le ete eis so. cele o.-0, 4c: 4Juje nie ins inte allan vdgusnatets ts miei ernie tater 2
XVIII. On the Classification of the Crustacea Malacostraca. By
WW. TCAD MANS DESC! ie eiole eiunie Giclee lagi. « «1p «spot inte salen ia 144
New Books :—Memoirs of the Geological Survey of the United
Kingdom. The Cretaceous Rocks of Britain. Vol. IL The
Lower and Middle Chalk of England. By A. J. JuKzEs-
Browne, B.A., F.G.S. With Contributions by Wi1L1am
Hr, F.G.S.—A Treatise on Zoology. Edited by E. Ray
Lanxrster, M.A., LL.D., F.R.S., &c. Part I. Introduction
and Protozoa 2h \ desis kee clas ete See ARP meio osha: ai reine 158, 159
NUMBER LXXV.
XIX. A Synopsis of the Suborders and Families of Teleostean
Fishes. By G. A. BoULENGER, FLRS. 0... eee eee eee eee ees 161
XX. On a Collection of Fishes made by Mr. John Graham at
Yunnan Fu. By C. Tare REeGAn, BA. cece cece eee eee eee 190
XXI. Rhynchotal Notes—XXI. By W. L. Disrant ........ 194
XXII. New Bats from British East Africa collected by Mrs. Hinde,
and from the Cameroons by Mr.G.L. Bates. By OLpFreELD THomas. 206
CONTENTS. v
Page
XXIII. Descriptions of new Species of Aculeate and Parasitic
Hymenoptera from Northern India. By P. Camrron 211
XXIV. Preliminary Note on certain Points in the Anatomy of
Eryx and other Bode, partly indicative of their Basal Position _
among the Ophidia. By Frank E, Bepparp, M.A., F.RS. .... 233
XXYV. Description of a new Genus of Spatangoids. By F.
Sbanrawrets Ve Es TR NOTA So ante sm ark, cca e SOO aan Ae atts 3 236
XXVI. Description of a new Barbus from Cameroon. By G. A.
BourmenGceEr; FRG. eer .t So eP oul T. SAGE IA) SORA Pas aae 237
XXVII. Notes on the Structure of the Teeth of some Poisonous
Snakes found in Travancore. By R. SaunkKARA Narayana PILiAy, 258
Obituary Notice: Dr. WirLIAM FRANCIS: oesci.. nos ee oe angie oeee 239
NUMBER LXXVI.
XXVIII. Descriptions of some new Species of Lepidoptera Hete-
rocera from Tropical South America. By HeErBERt Druce,
LULUS GM sOoe eMlor bie 0 DIC CBIR geIGe-C EI in EAL Pint toe ara ie rarer ieiieas 241
XXIX, New Forms of Saimiri, Saccopteryx, Balantiopteryx, and
Thrichomys from the Neotropical Region. By OLprirLp THomas. 250
XXX. Descriptions of new or little-known Fishes from Mexico
and British Honduras. By C. Tate Rea@an, B.A. ............5.
255
XXXI. Descriptions of Holocentrum oseulum, Poey, and of a new
Fish of the Genus Cextropomus. By C. Tarr Rreaan, B.A. ...... 259
XXXII. Descriptions of Two new Genera of Frogs of the Family
Ranide trom Cameroon. By G. A. BouLencER, F.R.S. 261
XXXII. Rhynchotal Notes—-XXII. By W.L. Distant .... 263
XXXIV. Description of a new Fish of the Genus Chetodon from
the New Hebrides. By C. Tare Reaan, B.A... 2. eee ees 276
XXXV. On some new Species of Hymenoptera from Northern
relists Sin yp brs CAMISRON giant ag saint a ga ea ld oh eel cae aye gm 277
XXXVI. An undescribed Genus of Coretzde from Borneo. By
ia PXMCPRESE AINE Ds: Sos ain << cbtic: seu cvaperonalu ames e cba'e tru Ware aise ns e«s.. 303
XXXVII. The Collections of William John Burchell, D.C.L., in
the Hope Department, Oxford University Museum :—
IV. On the Lepidoptera Rhopalocera collected by W. J. Bur-
chell in Brazil, 1825-1830. By Cora B. Sanprers, of
Lady Margaret Hall, Oxford. (Plate VI.)............ 305
XXXVIII. Note on an undescribed Weasel from the Atlas
Mountains, and on the Occurrence of a Weasel in the Azores. By
oe be NE eT EAM ON . dios, ein. 5 eck gesagt cated guysse od 323
New Book :—Report on the Sea Fisheries and Fishing Industries
of the Thames Estuary. Prepared by Dr. James McrRiz .... 325
Proceedings of the Geological Society ......eecsevevecenes 326—328
al CONTENTS.
NUMBER LXXVII.
Page
XXXIX. The Phylogeny of the Teleostomi. By C. Tarr ReGan,
BIAS (Plate VoL) os cbc hie ot isle codietee 7 heheh Ore ee BO fetta 329
XL. Rhynchotal Notes—XXIII. By W. L. Distant ........ 349
XLJ. The Collections of William John Burchell, D.C.L., in the
Hope Department, Oxford University Museum :—
IV. On the Lepidoptera Rhopalocera collected by W. J. Bur-
chell in Brazil, 1825-1830. By Cora B. Sanvrrs, of
Lady Margaret Hall Oxford ass sid.en deme: alas oaEPOO
XLII. Notes on Phasmide in the Collection of the British Museum
(Natural History), South Kensington, with Descriptions of new
Species.—No. I, By W. F. Kimsy, F.LS., F.ES,.............. 372
XLIII. On the Genus Ortmannia, Rathb., and the Mutations of
certain Atyids, By EH. L. BOUVIER ..........seeeeeeneee Aca 2s
XLIV. Notes on a new Species of Acts. By W. D. HenpERSon,
M.A., B.Se., Zoological Laboratory, the University, Aberdeen .... 381
> XLY. A new Bat from the United States, representing the Euro-
/ pean Myotis (Leuconoe) Daubentoni. By OLpriELD THomas ..., 382
= XLVI. Three new Bats, African and Asiatic. By OLpFIELD
THOMAS, ..52.:+% OO Oar Ocoae Catto mins ae Seo ot 384
XLVII. Notes and Descriptions of some new Species and Sub-
species of Mustelide. By G. KE. H. Barrurt-HamITon ........ 388
New Books :—Mostly Mammals. By R. LyprxkKrer.—Catalogue of
the Lepidoptera Phalznz in the British Museum. Volume LV.
Catalogue of the Noctuide in the Collection of the British
Museum. By Sir Gores F, Hampson, Bart.—The Fauna of
British India, including Ceylon and Burma. Published under
the authority of the Secretary of State for India in Council.
Edited by W. T. Branrorp. Rhynchota: Vol. UH. Part 1
(Heteroptera). By W. L. Disranr.—Memoirs of the Geo-
logical Survey. Palzontologia Indica. Series IX. The
Jurassic Fauna of Cutch. Vol. UI. Part 2. The Lamelli-
branchiata. No. I. Genus Trigonia, By F. L. Kircuty, M.A,,
Ph.D., Geol. Survey England. — Circulars on Agricultural
Economic Entomology. Issued by the ‘Trustees, Indian
MUSEO 1, )e's.3 @ ated ape talers sisi riage int fs slaraes wiepalaninualole apereus fe 395—399
Proceedings of the Geological Society ss seseseeeeeseeeees 399, 400
The Action of Human Serum on certain Pathogenic Trypanosomes,
Action of Arsenious Acid upon Trypanosoma gambiense, by
A. Laveran; Relations between the Development of the
Tracheal Apparatus and the Metamorphoses of Insects, by
Jules Anglas seem e were re rere rere r eer ereoereeereeeeee 401—4038
CONTENTS, Vil
NUMBER LXXVIII.
Page
— _XLVIII. On Mammals from Northern Angola collected by
ire Wo J; Ansorge: By OLprienn THOMA iscscsias gcse ene 405
XLIX. On Felis ocreata, better known as Felis caligata, and its
Subspecies, By HAROED SCHWANN ....c200c0. one nueva done es 421
L. On certain African Butterflies of the Subfamily Pierine. By
PEonennG. BUTLER. Ph.Ds, FDIS; &ei0 << 2octseces oo« sows slats 426
LI. Notes on Phasmide in the Collection of the British Museum
(Natural History), South Kensington, with Descriptions of new
Genera and Species.—No. II]. By W. EF. Kirsy, F.LS., F.E.S. .. 429
LIT. Diagnoses of Three new Species of Barbus from Lake
Victoria. By G. A. BouLenerr, F.R.S.
LIT. Descriptions of Three new Snakes. By G. A. BouLENGER,
F.R.S.
LIV. Descriptions of some new Species and Varieties of Cataulus
from the Collection of the late Hugh Nevill, ig By Hueu
MPCON font srays o/c ao Nov ha ay Raat tas apaventanns biisin’d + oid abeis eave bok 452
LV. Natural History Notes from H.M. Indian Marine Survey
Steamer ‘Investigator,’ Commander T. H. Heming, R.N.—Series
III., No. 1. On Mollusca from the Bay of Bengal and the Arabian
Sea. Bey Pri Ags Aly Mer Meeting cers Ss aks Siac weaken paso oi vn EES
New Books:—Memoirs of the Geological Survey of the United
Kingdom. The Cretaceous Rocks of Britain. Vol. III. The
Upper Chalk of England. By A. J. Juxes-Brownr. With
Contributions by Wi mLLIAM Hii, F.G.S.—Pictures of Bird-
iste fens.) HODGES Sender eset. « reese 470, 474
Teleostome Phylogeny : a Correction ..........cscccceccees ose. 475
Index Cessa peur egerresesceee es weve eevee ereee eer seer eeererereeees 476
PLATES IN VOL. XIII.
Prototheca of the Madreporaria.
Colpoglossus Brooksii.
Map: W. J. Burchell’s Travels in Brazil.
Stridulating-organ in Scorpions,
Depastrum cyathiforme.
Lepidoptera Rhopalocera from Brazil.
Phylogeny of the Teleostomi,
THE ANNALS
AND
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]}
~ neki ecececeoerne: per litora spargite museum,
Naiades, et circiim vitreos considite fontes:
Pollice virgineo teneros hic carpite flores:
Floribus et pictum, dive, replete canistrum.
At vos, o Nymphe Craterides, ite sub undas ;
Ite, recurvato variata corallia trunco
Vellite muscosis e rupibus, et mihi conchas
Ferte, Dez pelagi, et pingui conchylia succo.”
N. Parthenii Giannettusi, Bel. t.
No. 73. JANUARY 1904.
I.— The Prototheca of the Madreporaria, with Special
Reference to the Gencra Calostylis, Linds., and Moseleya,
Quelch. By Henry M. Bernarp, M.A. Cantab., F.L.S.
[Plate I.]
Tur task I have set myself is to sketch what appears to have
been the leading features in the evolution of the Madrepo-
rarian skeleton. The researches on which the arguments are
based have been almost entirely limited to the skeleton, not
because the importance of a close study of the soft parts is
not recognized, but because, for the attainment of accurate
results, the widest possible survey of homologous structures is
indispensable. This condition can never be supplied by the
soft parts. ‘They can at the most be studied in a few recent
specimens, whereas the vast majority of the forms presented
by the Madreporarian system are fossil. Further, let me
add in passing that I do not believe that the study of the
individual development of a few living forms can by itself
establish anything certain about the past history of the group,
for the simple reason that we cannot tell whether any special
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 1
2. Mr. H. M. Bernard on the
developmental feature is a repetition of some ancient con-
dition or a recent adaptation *. As I have already often
maintained, lines of phylogenetic growth can only be satis-
factorily established by the discovery of connected series of
variations, morphologically and chronologically arranged.
The skeleton alone can supply us with such series, and that
of the corals probably with a more complete series of forms,
extending from the Paleozoic era to the present day, than will
ever be obtained of any other animal group. Whether, there-
fore, the skeleton be of great or of little importance in itself
in the morphology of the corals, it alone supplies us with
what we want—a continuous series of homologous structures.
On this account alone, then, when our aim is taken into
account, we are obliged to confine our attention to the
skeleton.
As a matter of fact, the skeleton is of paramount importance
in the coral organism. There is a sameness in all the soft
parts which limits their morphological importance in any
comparative study. ‘Their chief variations may, for practical
purposes, be said to be repetitions of the variations of the
skeleton which they secrete. The skeleton is, par eacellence,
the chief structural feature of the coral, its relation to the soft
parts being extremely simple. It is, as we now know, thanks
to the researches of von Koch, Heider, Fowler, Bourne,
Ortmann, and Miss Ogilvie, an excretion of the basal parts
of the outer wall of the body, and hence morphologically it is
external to the organism. At times very complicated, it is
an organ of protection and support for the body of the polyp,
or, in colony formation, for the colonies of polyps, the polyps
themselves, thus protected, having, as arule, remained simple
and primitive. ‘The corals, indeed, present us with a group
of organisms still primitive enough to illustrate the fact that,
of the earliest niorphological modifications of the living
matter, skeletal formations were the most pronounced. ‘This
is strikingly exemplified by the Foraminifera and Radiolaria,
in which there is a wealth of skeletal formations with little
or no visible variation of the soft matter. Again, in the
sponges the skeletal variations far outrun those of the soft
parts. ‘The same is true of the stony corals.
In what follows, therefore, I shall make no detailed refer-
ence to the soft parts or to the excellent work which is being
done with their help by Dr. Duerden towards the elucidation
* N. Guldberg and Nansen, “On the Development and Structure of
the Whale,” Bergens Museum, 1894, p. 89; also Sedgwick, Proc. Fourth
International Congress of Zoology, 1898, p. 74.
Prototheca of the Madreporaria. 3
of the same problem as that which here interests us. I shall
confine myself solely to showing how some of the chief
transformations of the skeleton can be linked into series and
how, in a few cases, the causes which led to those transforma-
tions are apparent. We are justified in hoping that the
conclusions obtained from the continued studies of the soft
parts on the one hand and of the skeleton on the other will
ultimately coincide.
I wish to make it specially clear that only a few of the
lines of modification can be dealt with, but those few, being
some of the earliest, are, I believe, the most fundamental and
important for the elucidation of all the later transformations
of the coral skeleton. To deal with the whole of these latter
would be to write a complete systematic account of the stony
corals. This is the aim of the great catalogue now being
prepared and published by order of the Trustees of the
British Museum, and must be a work of years *.
The researches of the writer in reference to this work so
far hardly entitle him to speak with confidence on any other
of the larger divisions than the Perforata; no other has as
yet been systematically dealt with by him, at least in the
thorough manner required for a British Museum Catalogue.
It would not, however, have been possible to discover the
morphology of these highly specialized Perforate forms
without a study of and constant reference backwards to earlier
and simpler types. In this way certain lines along which the
stony corals have travelled, viz., those leading from the most
primitive to the most specialized, have been growing clearer.
* The last attempt to deal with the whole of the coral system in the
‘ Hist. Nat. des Coralliaires’ of Milne-Edwards and Haime, completed
in 1860 by Milne-Edwards alone, was founded on comparatively small
collections and written at a time when the relations between the skeleton
and the polyps were not understood. The excellence of the results which
were nevertheless obtained is, on the one hand, a tribute to the genius of
the great French naturalists, and, on the other, a witness to the compa-
rative unimportance of the polyp, morphologically, as compared with the
skeleton. S:
The new catalogue projected by the authorities of the British Museum,
and rendered necessary by the immense increase in the collections due
especially to the sending out of scientific expeditions, was started in 1876,
but was interrupted by the death of Dr. Briiggemann, who was engaged
for the purpose. After fourteen years Mr. George Brook undertook the
work, but again death intervened soon after the first volume was published
in 1893. Two years were again lost, when the present writer was
appointed to continue the work. There are now four volumes published,
and the fifth is rapidly approaching completion. Each volume is practi-
cally a monograph of one, or at the most two, genera, and, like the earlier
attempt of Milne-Edwards and Haime, it now describes the fossil as well
as the recent forms.
1*
4 Mr. H. M. Bernard on the
The following pages sum up the principal conclusions he has
arrived at.
The most important stage to establish in an evolutionary
history is the first, or that which we may consider as the
first, inasmuch as from it all the modifications we wish to
compare can be deduced. ‘The first stage in the evolution of
the coral skeleton was first dimly recognized by me in the
minute saucer-shaped cups of young Madreporidan colonies—
so young as to consist only of a parent calicle and one or two
daughters. In none of the Madreporids have I yet found the
earliest stage in which the cup containing the parent alone
was cup-shaped. Such astage, however, may be legitimately
assumed.
The discovery of such colonies made three points clear to
me :—
1. The parent calicle of a colony rises out of a basal cup—
the PROTOTHECA *.
2. This prototheca is not a composite structure, but a
morphological unit, the rim of which can be bent up, flattened
completely down, and indefinitely expanded in any direction
as a film, from the upper surface of which, as originally
from within the cup, the coral skeleton arises.
3. This film is the EPITHECA t.
These conclusions received complete confirmation from a
study of the Paleozoic form Favosites and of its modern
descendant Alveopora. I have already described and figured
the prototheca of the latter genus}. Its rim, as shown in the
figures referred to, does not usually flatten down, but grows
upwards and outwards to form the irregular film-like invest-
ments characteristic of the colonies of this genus.
In both cases—that is, in Madreporide and Favositide
alike—it was easy to see the bars of the intracalicular skeleton
rising directly out of the wall of the cup as internal projections
from its surface; this point is of importance, because
von Koch, whose developmental researches also revealed to
him the prototheca, was led by what he saw to regard it as a
composite structure consisting of a basal portion (‘‘ Basal-
* Lindstrom suggested the word “ initium” for the earliest cup-like
skeleton ; the term ‘“ prototheca” was suggested to me in conversation
by my friend Prof. Jeffrey Bell.
t+ The fact that the skeletal elements rise from the surface of the
epitheca was pointed out by Martin Duncan in 1884 (Journ. Linn. Soc.,
Zool. xvii. p. 861) as indicating the importance of that element of the
coral skeleton.
{ Journ. Linn. Soc., Zool, xxyi. 1898, p. 495, pl. xxxiii.
Prototheca of the Madreporaria. 5
platte,” sole) and of a peripheral portion (epitheca). This
appears, however, now to have been a too literal rendering of
the facts of his observations, for no one who had seen several
of these epithecal saucers of different sizes and with edges
turned up to different heights at different curves, and the
skeletal bars springing indifferently from the sides and the
base, could possibly divide it into a basal and a peripheral
portion.
Besides, in a young saucer-shaped colony it is obvious that
the turned-down side (the “‘ epitheca’””) of the parent becomes
the “basal plate” of the daughter, and in this successive
flattening down of the rim we can see the explanation of the
characteristic wrinkled appearance of the supporting epitheca
of so many horizontally expanding corals, whether single or
compound. Each furrow represents a pause in the outward
growth long enough to allow the rim of the widening saucer-
shaped epitheca to grow upwards a short distance. The
next period of growth carries it downwards and outwards
again. This process has been actually seen by Lacaze-
Duthiers * in the development of Balanophyllia regia. ‘This
writer observed three attempts of the basal secretion of the
larva to turn up to form a cup or “envelope calicinale,” but
they were always futile ; the septa overran them and the edge
was flattened down again and continued as a_ basal secretion
goer fig. LO):
Before continuing with the history of this prototheca—that
is, with our account of some of its earliest modifications—it
will strengthen our argument to mention a few instarices in
which earlier writers have come near to recognizing this
identity of the prototheca with the epitheca. As we might
expect, such an identification would be more probable in
relation to Paleozoic forms, in which the primitive cup
remained longest in evidence and had not become so distorted
and masked as it is in the majority of the modern forms.
Milne-Edwards f, in describing the Paleeozoic genus Za-
phrentis, which, from its appearance in time, might have
been expected to have retained the prototheca, says that it is
completely surrounded by an epitheca, Nicholson could not
distinguish the epitheeca of these same corals from the wall.
Miss Ogilvie } declared that in Zaphrentis the epitheca
“supplied the primitive base and periphery in one,” and
again that the primitive wall of corals was epithecate ; and
* Arch. Zool. expérimentale, (3) vol. v. 1897, pp. 179-183 & 230, pl. x.
figs, 19-24, fr.
+ ‘Les Coralliaires,’ iii. p. 385 (1860).
{ Phil. Trans. 1896, p. 320 Ke.
6 Mr. H. M. Bernard on the
again the same writer recognized the wall of Zaphrentis as
“euthecate,” which means that the persistent prototheca in
these early corals is the eutheca or true primitive wall of
Heider and Ortmann, as compared with which all other thecz
are secondary. ‘To this last opinion we shall return.
Mention should also surely be made of Ludwig *, who, so
long ago as 1866, attempted to found a classification upon
his recognition of the prototheca as the primitive shell
(“ Gehiiuse”’) of the coral polyp. But beyond the interest
attaching to the fact that he thus emphasized the importance
of the prototheca in Madreporarian morphology his work has
no value, for he was led astray in his further analysis by a
fancied analogy with the shell of the mollusk.
In the present paper, then, we start again from the recog-
nition of the prototheca, but this time, avoiding Ludwig’s
mistake, we shall try to analyze some of the actual modifica-
tions which this primitive coral skeleton has undergone in the
progress of its evolution. So far from being as simple as
Ludwig appears to have assumed it to be, it isa task of
considerable complexity to follow and of no small difficulty to
describe. This paper, indeed, was begun five years ago, and
has been frequently rewritten.
As I have shown, those parts of the coral skeleton called
epitheca must for the future be referred to the rim of the
prototheca. ‘Thisseems simple and clear now, but in the past
the epitheca has been the stumbling-block of coral morphology.
It has been this for the very reason that it waited for the
discovery of the prototheca before there was any possibility of
its elucidation. The fact of the confusion in the prevailing
views as to what the epitheca is is familiar to every coral
student. For instance, Prof. Gregory, of Melbourne, after
all his years of work at corals, characteristically summed up
his despair of ever making anything out of it by declaring
that ‘“‘there was no part of the coral skeleton over which
more time had been wasted” tf. This attitude and that
which is taken in this paper are poles asunder. Between
these two, authors and text-books hover. None are so bold
as Prof. Gregory, yet none have succeeded in formulating an
intelligible doctrine.
We may here state that there is ample excuse for this
confusion, for even now that we know that the epitheca, as it
occurs in the majority of specimens, is only an extension of
the rim of the original cup, still in each case the problem as
* ‘Paleontographica,’ vol. xiv.
+ Palontol, Indica, ser. rx. vol. ii. p. 11 (1900).
Prototheca of the Madreporaria, i
to how this can be requires unravelling. It may, for in-
stance, be the rim extended indefinitely and continuously as
a chalky film round a colony (e. g. Alveopora), or, again, it
may be discontinuous and represent the separate rims of an
aggregation of corals, each with its own cup, as in so many
Paleozoic forms. In this case it depends upon the way in
which the corals are aggregated whether the rims are easy or
difficult to recognize. Add to these difficulties the fact that
apparently any part of the surface of a polyp may diz down
and secrete a calcareous film * which is purely adventitious
and has no morphological significance, and it is obvious that
until we had a key to its elucidation the epitheca could not
fail to be a source of bewilderment.
Diagram 1 (PI. I.) shows the three earliest growth periods of
a primitive Madreporarian skeleton. All that we see is a deep
cup with three tabular floors. 'The process is explained in
diagram 2, in which we see three cups progressively modifying
their shapes. The lowest of these is the prototheca in the
strict sense of the wordt, bat it is advisable to apply the
term to all simple repetitions with free edges. Fig. 2 is so
far diagrammatic, inasmuch as with cups of this shape it is
impossible to say how far the rim of each cup extended before
the soft parts of the base of the polyp became detached from
the base of its prototheca. Cases, however, do occur in
which the change in the shape of the new thece was rapid,
and for this and also for other reasons the rims of the separate
* The formation of calcareous films somewhat irregularly over the skin
of corals is hardly to be wondered at. The prototheca was but the
primitive secretion of the basal portion of the polyp, forming a protective
cup into which the animal could retract the oral and exposed end of its
body. Above the rim of this cup calcareous secretions were not usual,
otherwise they would have interfered with the process of retraction, but
the power of secreting them was not lost. Indeed, some forms actually
secreted lids, which, when the polyps retracted, closed down over the
prototheca (Calceola, Goniophyllum). A histological difference between
these secondary films and true epitheca may sometimes be noticed. The
former may be built up of separate plates, each of which starts round
some point of the skeleton and grows by concentric increments.
+ The prototheca is here drawn quite diagrammatically. Figure 8,
after Lacaze-Duthiers, is one of the best figures from life. My own
figures, already referred to, of a young Alveopora are of a prototheca
somewhat distorted. Theoretically we might expect a slight constriction
above the flattened sac, for as the soft larva settled down we might
expect its aboral end to flatten out somewhat wider than the neck
carrying the oral disk and tentacles. The base of the second prototheca
might easily be rounded or pointed, for it would hang down in the
hollow of the prototheca proper. The later development of convex tabulee
and vesicular dissepiments may have been due to the pulls of mesenterial
muscles.
8 Mr. H. M. Bernard on the
cups may be distinguishable. For instance, the development
of exsert laminate septa may lift the cups above one another
(see Pl. I. figs. 3, 11, 12).
Fig. 8 refers to Montlivaltia, of especial interest because it
was the irregular bands of epitheca round specimens of this
genus which induced Dr. Gregory to give up this element of
the coral skeleton in despair. We shall now show that an
understanding of these bands is essential to a true insight
into the morphology of the skeleton.
It is frequently stated * that in Montlivaltia there 1s
epitheca, but no theca. There was, however, certainly a
prototheca, and examination of the coral shows that the
successive protothece gradually flattened out until, after
reaching a certain size, they formed a series of flat saucers
(tig. 8, e, ee...) of nearly uniform size, and piled up one
above the other as tabule with edges which may either only
just reach the surface or be bent sharply upwards to varying
heights according to the accidents of secretion. On the left
of the figure a few of the septa are shown supporting and
raising the successive saucers above one another. ‘The septa
of each polyp continue those of that which went before it, so
that these radial structures naturally run up continuously
through the whole skeleton... On the left of the diagram the
saucers alone are shown in optical section as a series of flat or
wavy floors with turned-up rims.
Here, then, we have the three facts necessary for the
understanding of the case in hand :—
1. A series of shallow thecee or protothecal saucers ending
abruptly at the surface or with edges bent up externally.
2. ‘The septa which, being exsert, support and lift these
saucers above one another, so that, while the septa are con-
tinuous, the rims of the cups may be free and separate, or,
when bent up, may run together as irregular epithecal bands.
3. ‘Lhe extreme irregularity of the bands is due to the want
of uniformity in the height to which the secretion of the rims
of the saucers, if bent up, extends.
These three factors fully explain the puzzle presented by
the epitheca of Montlivaltia.
It is obvious that in diagram fig. 3 the saucers might
contain not single polyps, but gradually expanding colonies
* E. y., by Miss Ogilvie (/. c. p. 158), who, however, followed Milne-
Edwards and Haime, who wrote with reference to A mplevus, in which
the succession of saucer-shaped protothece is very pronounced :—
“Quelquefois méme la muraille purait manquer et Je polypier nest
constitué que par une série de cornets tres evasés et naissant les uns
au-dessus des autres’? (Ann, Sci, nat. (5°) ix. p. 84, 1848).
Prototheca of the Madreporaria. 9
(ef. the minute colonies of Madreporids already mentioned).
Such series of gradually expanding colonies might grow into
columnar or massive stocks widening at the top. In all such
stocks the tabula which run through them must be regarded
as the floors of successive saucers. This is well exemplified
‘in the genus Goniopora, as I have already explained *. In
this genus too we have, as we have in Montlivaltia, irregular
bands of epitheca running round the stocks. These are the
rims of the protothecal saucers showing irregularly at the
surface. In Alveopora the rims all run together to form
continuous epithecal investments, except, perhaps, in their
branching forms, in which the protothece may be lifted up
.above one another by the growth of the spiny septal skeleton.
For an understanding of the morphology of the coral
skeleton we must bear in mind that essentially the same
process, viz. @ succession of epithecal cups or saucers, occurs
throughout the whole of the Madreporaria. They may be
simple conical cups fitted one into the other (Zaphrentis) or
flat plates piled up (Montlivaltia, Goniopora), or their epithecal
floors may be thrown into complicated folds and both the
cup and its repetitions may be difficult to unravel, but the
fundamental principle is the same throughout. There is only
one group I can think of in which the epitheca is not nor-
mally repeated, namely in the highest Madreporids—Madre-
pora, Turbinaria, Montipora, Astreopora, and their simpler
ancestors the Kupsammiids. In these the purely septal
skeleton rises rapidly above the original flattened prototheca
which is then left behind. This is the reason of that well-
known characteristic of these forms that the calicle cavities
run continuously for long distances through the skeleton.
We repeat, then, for the sake of emphasis that wherever
the epitheca occurs it represents the rim or the coalesced rims
of one or more protothecal cups or saucers, the floors of which
are represented by the tabulee. In any individual case the
tabula below the living layer is the nth repetition of the
original prototheca of the parent polyp.
The main problem, then, of the student of coral morphology,
that is, taking the skeleton alone into account, is to trace the
various moditications of the prototheca from its earliest simple
cup stage to the many different shapes and positions it now
assumes and occupies as part of the coral skeleton.
Roughly speaking, we may say that there are two periods
in the evolution of the Madreporaria—that in which the
prototheca, though modified, remains in evidence, and that in
* Cf. vol. iv. Brit. Mus. Madreporaria, p. 24, diagram A,
10 Mr. H. M. Bernard on the
which it has disappeared from view or is difficult to unravel.
Only in the few Madreporids (the chief families of the
Perforata) above mentioned can it be said to have been aborted,
and then only in a limited sense, for the whole coral skeleton
is its product. If the original rim of the cup is replaced as
the edge of the theca by new thece formed either by the
rising up of concentric folds from its floor or of radial plates
from its sides, or by complicated combinations of these two,
these new thece are strictly infoldings of the prototheca,
The prototheca, then, however obscured its early cup shape,
being replaced by secondary cups produced by its own
infoldings, remains throughout the fundamental element in
the Madreporarian skeleton.
I propose here to trace some of the more obvious trans-
formations of the prototheca, treating them entirely morpho-
logically—that is, simply as forms which admit of explanation
and deduction from simpler forms, and without regard to their
real phylogenetic sequences.
The working out of these latter—that is, the attempt to
discover the real places of these transformatory processes in
the genealogy of the Madreporaria—must be a work of time.
I am convinced, however, that it will at once give a new and
much needed interest to the student of the stony corals.
We return, then, to our simplest form (diagram fig.1). It
shows us a conical cup standing on a flattened slightly ex-
panded base and gradually thickening upwards. The problem
of increasing instability must obviously have been one of the
jirst which the polyp inhabiting sucha skeleton had to solve.
I shall endeavour to show that the earliest divisions of the
Madreporaria were due to the different ways in which this
problem was solved.
I. Falling over and recovery of the upright position —The
simplest of all methods was to fall over so that the flesh of
the polyp could come once more into contact with the sub-
stratum and secrete a new cementing layer where it touched.
From this new base the polyp could bend upwards once more
securely attached. ‘The following is some of the evidence
which shows that this actually took place :—
(a) The earliest period is specially characterized by the
great number of single corals which are conical but curved.
‘he curve is exactly what is required ; that is, it is most pro-
nounced at the tip, e. g. Zaphrentis, Menophyllum, &c.
(6) All these curved corals have what is known asa fossula,
that is a deep depression within the calicle and most frequently
on the convex or what is called the ‘ dorsal” side. The
fossula has a very simple explanation, if the assumption of
Prototheca of the Madreporaria. 11
the falling over is correct (see diagram fig. 4). As the soft parts
detach themselves from the base of the prototheca they might
be expected to bag down, and they will continue to be acted
upon by gravitation and drawn over towards the convex
side of the coral until the vertical position has been regained.
It is possible that this bearing over to the side may be due to
the efforts of the polyp itself to bend up, but gravitation is a
causa efficiens.
In some forms, however, the fossula is not on the dorsal,
but on the ventral side. ‘There is abundance of scope for
variations of all kinds: a deep cup (that is, the cup of a
polyp which grew very slowly in width, for instance) would
lie very prone and its fossula would fall over to the dorsal
side (diagram fig. 4); but a shallower more open proto-
theca (that is, one in which the polyp grew very rapidly
in width) would, in the prone position, have one (the
‘“‘ventral”’) wall nearer the vertical, and this would keep
the skin of the point while it hung loose for the while near
the ventral side, and the fossula would consequently also
appear on this side (diagram fig. 5) *
(c) The falling over of the prototheca will explain the
departure from a strictly radial symmetry of the septa seen in
these curved Paleozoic corals. It is obvious that, as the
coral is bending to the vertical, seen from above, the septa
would have the arrangement shown in diagram fig. 6, which is
after the classical figure of Kunth showing the septal formula
typical of the group called Rugosa. ‘The position of the
fossula with relation to this modification of the septal arrange-
ment shows that this is the true explanation. Further, it has
long been known that, as such corals gradually reacquire a
vertical position, the septal arrangement slowly gives up the
bilateral and returns to the radial symmetry. ‘Thus the
character on which it was proposed to found a great division
of the stony corals was nothing but a slight mechanical
* This is not the first time that this origin of the fossula as a repetition
of the tip of the prototheca has been recognized. Ludwig's figures made
it quite clear in 1866 (‘Corallen aus paliiolithischen Formationen,”
Palzeontographica, xiv. 1866). But, regarding the skeletons as analogous
to the shells of mollusks, to whose shapes he thought they were adapted,
he failed entirely to understand the true character of the coral skeleton or
of the causes of its changes.
The use assigned in text-books to the fossula, viz. as a sort of erypt for
the sexual products, is probable enough, but need not have been the cause
of its origin. I fail to see the evidences for the existence of more than
one true fossula in any coral I have examined. Superficial irregularities
in the septa, due perhaps to the presence of sexual products, may be quite
distinct from the true fossula, A longitudinal section or a fracture
showing a complete tabula is the only evidence which can be relied on,
12 Mr. H. M. Bernard on the
adaptation to a passing phase in the life of each individual
coral. But it is only fair to say that the whole tendency of
recent works on corals has been to discover the invalidity
of the supposed division Tetracorallia,
Into the interesting questions which this suggests as to the
value of the existing divisions of the corals, we cannot here
enter, but content ourselves with merely pointing out that
while probably all the very earliest corals fell over and, if
they bent up again, became Tetracorallia during the process,
it is possible that many, which later had learnt a different
method of acquiring stability, might easily be knocked over
and in their efforts to become vertical again might become
Tetracorallia by accident.
(d) The falling over of the prototheca enables us to find an
origin for several groups which are usually regarded as corals,
but whose position is still a matter of uncertainty. It is quite
within the limits of probability that a certain number of these
overturned polyps in their small protothece should remain
prone and bud in this position. One such case we know of
for certain (see p. 28, on Heliolites). We ask whether the
creeping branching stocks of Aulopora might not also have
been formed by the early budding of a parent whose proto-
theca had fallen over.
From Aulopora the genus Syringcpora might be deduced.
Syringopora is said to begin with the same horizontal creeping
stock as Aulopora, and then to bend up and form its tufts of
wavy tubes freely communicating with and supporting one
another. In these erect tubes very irregular tabule are formed
by the constant rising of the polyp in the tube as the latter
lengthens. The very presence of tabulz and of the rudi-
mentary septa, consisting of rows of points, clearly indicates
an affinity with early Madreporaria. Add to these the proto-
thecal outer covering, and we have the same three structures
which make up an Alveopora or a Favosites. It is only their
dispositions and the relative developments of the parts which
differ *.
Halysites could also be deduced from such a prone theca by
ra} id continuous budding, in such a way that the parent and
its buds bent up in rapid succession into the vertical, as
shown in the diagram fig. 7, each then continuing to grow as
a thin flattened tube. ‘hese in contact and mutually sup-
porting one another would supply the typical skeleton of this
* The apparent affinity between Syringopora and Favosites has been
pointed out by Mr. Bourne (Phil. Trans. vol. 186 B, p. 474). But Favosites
is structurally indistinguishable from Alveopora, and was not therefore an
Alcyonarian (Proc. Linn, Soc., Zool. vol. xxvi. (1898) p. 495.
Prototheca of the Madreporarva. 15
remarkable genus. We have the same three elements, proto-
thecal tubes, tabule, and spiny septa *.
(e) The habit of falling over is known still to occur in the
genus Flabellum.
(f) Lastly, I appeal to the modifications of the prototheca
which will be described in the following pages, every one of
which may be regarded as an adaptation for the purpose of
solving the problem of vertical stability, that is, how to avoid
the natural consequence of having to stand on a point while
continuing to grow in height and bulk. For we are surely
justified in assuming that the falling over at the very outset
of life of an organism intended, if we may say so, to stand
upright, would mean considerable loss of time and energy
during the reattainment of the upright position. Such a loss
might be expected to delay budding, and it is probable that
we may have to take this into account in our ultimate classi-
fication. We may have to form a group which arose from the
early budding of parents still in their protothece (sens. sér.),
and this would include such forms as Aulopora, Syringopora,
and Halysites, in all of which the protothece fell over, and to
these we might add Chetetes arising probably by fission.
Whether the prototheca also fell over in this last case I have
not ascertained. Such a group arising from parents still in
their protothece proper, would stand in contrast to another
group in which the budding was delayed until the polyp had
grown considerably larger and had again assumed the upright
position, and our divisions of these latter would have, in the
first instance, to be based upon the methods adopted to attain
this end.
II. Radicle-formation.—This process has been carefully
studied and described in Flabellum by Lacaze-Duthierst. A
small portion of the lip of a prototheca bends over until it
adheres to the ground (see diagram fig. 8a,6). I have myself
seen a similar process as an occasional thing in young colonies
of Alveopora. It is difficult to see how the great pear-shaped
colonies in this latter genus could possibly stand upon the tip
of the original prototheca without gaining support on this
principle. Extensive droopings of the rim till it touched the
ground with subsequent bends up again are probably more
common in this genus than the formation of thin radicles.
Root-processes may come from the rims of different proto-
thecze in those cases in which the corallum is built up of a
* Cf. Fischer-Benzon, Abhandl. wissench. Ver. Hamburg, Bd. y. 2
(1871), pp. 1-28. a : ‘2
+ Arch, Zool, expér. (3) ii. 1894, p, 445, pl, xviii.
14 Mr. H. M. Bernard on the
series, like those shown, for instance, in fig. 3. Omphyma is
a typical case. .
But this whole process need not detain us; it has no serious
morphological value, being obviously a device for a certain
end. When that is attained, it has no further influence on the
shape of the skeleton *.
III. Karly flattening out of the Prototheca.—It is obvious
that if, by any means, the early prototheca could be trans-
formed rapidly into a disk, a broad base could be acquired by
the skeleton which would keep it upright. It seems to me
clear that the morphology of many of the Paleozoic corals can
be explained on this hypothesis. But the different ways
adopted of so changing the primitive conical prototheca seem
to have been very numerous, and a review of the forms from
this point of view is a desideratum. It is, I believe, along
this line that we shall find a more natural set of characters for
the revision of such groups as those now included, e. g., in
the Cyathophyllidee, than any now adopted.
In the present place I can only give a few samples, and,
to avoid doubt as to the forms meant, I propose to take
as examples certain well-known figures accessible to every
student.
“ Zaphrentis gigantea,’ pl. iv. of Milne-Edwards and
Haimes’s Pol. foss. d. Terr. paléozoiques. I give this in
passing because it is interesting as a very irregular method
of acquiring a broad flat base. Diagram fig. 9 (PI. I.) shows
my interpretation of the process. It may be that the coral
did not actually become detached and fall over, but that the
method may be compared with radicle-formation, only, instead
of a narrow lip, the whole side of the prototheca bent out-
wards and apparently became cemented to the substratum.
It will be seen from a comparison with Milne-Edwards and
Haimes’s figures that in this diagram I am assuming what
the early transformation of the prototheca was from the shape
of the tabule in the adult stages; and this is, I believe,
perfectly justifiable. Unfortunately not sufficient attention
has yet been paid to the variations of the prototheca, which
are still to be discovered. In certain types of modifications,
e. g. those shown in diagrams figs. 11 and 12, the very earliest
* Miss Ogilvie’ssuggested origin of the Perforata froma great elaboration
of root-processes so as to form the reticular coenenchyma is very ingenious,
But it is hardly borne out by the development of young Madreporidan
corals in which the cup- or saucer-shaped prototheca persists as a basal
epitheca (see p. 4), and being flattened out from the first has no oppor-
tunity to form radicles,
Prototheca of the Madreporaria. 15
modifications can still be easily seen; but in others they are
at once obscured, incorporated perhaps in the subsequent
stock, or, again, in others worn or dissolved off.
The tendency has been to regard the variations at the
extreme bases of these Palzeozoic corals as accidental, and hence
of no real value in classification. This view will, [ hope, for
the future be abandoned and special attention be paid to any
traces which can be seen of the different ways in which the
early prototheca was modified. It is quite possible, indeed,
that many will be found to have been lar gely accidental, For
instance, such a bend over as that shown in diagram fig. 9
may have been pure accident. The same may be said of
radicle-formation. More extensive comparisons, especially
from this point of view, are necessary before we can say
whether such a method of forming a broad base as that shown
in fig. 9 became habitual in any group of early corals or not.
It is worth noting that other corals are known which adopted
it, as, for instance, the Dipterophyllum glans of Roemer
( Lethea Geognostica,’ 1. p. 371).
More interesting, how ever, than these irregular, one-sided
bendings over are those which took place more or less symme-
trically all round. ‘The most perfect of these methods, and, I
believe, one of the most recent, is certainly that in which the
edge of the prototheca is very early bent down, that is before the
cup has any real depth, as already described above (see p. 5)
as being the case in the Perforata. The successive bendings
down and attempts to bend up again of the edge of this proto-
theca will, as we have seen, account for the successive
wrinkling of the flattened epitheca (see diagram fig. 10). The
Perforata owe their leading characteristics to this fact, that
upon their flattened prototheca or epitheca a purely septal
theca arises, and as the polyps bud the new thece are also
septal and may mount upwards to form enormous stocks
built entirely out of radial septa mutually supported by con-
centric synaptaculz, leaving the epitheca, as in Turbinaria,
as a film beneath the base of the stalk,
On the solution of the question as to when this very early
flattening out of the prototheca arose depends that of the first
appearance of the Perforata in the coral system. We get
what appears to be a flat, very wrinkled epitheca in Cyclolites
of the Secondary epoch, and again still earlier in the Paleozoic
Paleocyclus. But an examination of specimens of these at
once shows that their flattened epithecee were not continnous as
in fig. 10. In Paleocyclus the conditions may be ec.
by the diagram fig. 11, and for Cyclolites by diagram fiz.
16 Mr. H. M. Bernard on the
the tabule in this latter case being represented internally by
vesicular dissepiments*. In these cases, then, instead of
there being one continuously expanding prototheca, there was
the usual repetition of protothecee which is so patent in the
Paleozoic forms and still persisting, though disguised, in all
corals. Even in the Perforata with tall conical septal calicles
it must occasionally reappear, while in forms like Porites and
Gontopora it is very marked (see above, p. 9).
These diagrams (11 & 12) are instructive because we see in
the Silurian Paleocyclus that the original conical shape of the
prototheca was not yet quite got rid of but persisted as a kind
of stalk, whereas in Cyclolites it was quite flattened out. ‘The
-process of flattening was apparently a slow one, and we
may assume that the earlier forms always started from a deep
prototheca, however rapidly (as in the case of Palcocyclus, tor
instance) the following protothecze may have flattened out.
Only in time was the flattening-out process so antedated that
the very first larval prototheca appeared as a flattened saucer.
And then, again, it was necessary to wait for the development
of a septal theca to take the place of the flattened prototheca,
before the latter could be lett to grow outwards continuously
as a mere basal support. One factor in bringing about this
gradual flattening of the prototheca, as seen, for instance, in
Cyclolites, might perhaps be seen in the delaying of the
secretion of the rigid walls of the cup, which was probably
rendered possible in the case of those forms which produced
well-developed radial or septal theca, the formation of which
might, in the early stages, use up the available material fT.
‘There was, therefore, apparently a long period during
which the rim of the prototheca was undergoing modification
in the direction of bending outwards and, if one may so
describe it, a period of uncertainty and hesitation. I am
convinced that the gradual steps by which the various flattened
* Tabule are secreted when the whole basal skin becomes detached at
once and secretes a new continuous floor. Dissepiments are the secretions
of portions of the skin coming loose at different times. We may see two
reasons for this partial detachment, and, these if correct, would throw
some light on the distribution of vesicular dissepiments :—(1) the mus-
cular attachments of the mesenteries buried in the skeleton may hold the
skin down at definite spots ; (2) the original floor becomes divided up by
radial septa, and thus the skin could not come off in one continuous
sheet.
In Cyclolites the rims. of the tabule, the internal parts of which are
broken up into vesicular dissepiments, can be traced round the corallum
as sharp lines (see fig. 12).
+ Lacaze-Duthiers, /. c., found that the septa could be the first skeletal
elements produced in developing Perforates, whereas phylogenetically the
prototheca came first.
Prototheca of the Madreporaria. ay’
protothecs were brought about deserve much more attention
than has ever yet been bestowed upon them. While I would
not deny that the rise of the radial ingrowths from the inner
(or upper) face of the prototheca, that is the septa, on which
Milne Edwards’s classification is mainly based, may not supply
during this period the best taxonomic characters, I still do
not think that the variations in the curve of the protothecal
rims, or, in other words, the shapes and dispositions of the
tabulee, can be so completely ignored as has hitherto been
done. A few examples will show what I mean.
Diagrams figs. 13 e-f show some of the forms assumed by
the prototheca of adult single Paleeozoic corals. They were
built up of series of such protothece fitting into one another
and usually raised above one another, sometimes by septal
folds or ridges, sometimes by vesicular arrangements of the
tabule of which only the edges showed clear and sharp, or
sometimes the sloping sides being vesicular, while the more
or less flattened bases are smooth.
It is impossible now to say how far these foldings outwards
and downwards of the rims are of the nature cf accidental
variations. But until we know I ean hardly think it right
to ignore them so completely as has been done, say, in the
genus Cyathophyllum as given by Milne-Kdwards and Haime.
For instance, we find specimens called Cyathophyllum which
show the prototheca of the shape given in fig. 13a (e. g.
C. turbinatum,Goldfuss*, said by Milne-Hdwards and Haimet
to be C. ceratites, although they themselves give a figure
of it which appears to have the prototheca of the form 13 h).
Again, Goldfuss (/.c. fig. 8d) gives other figures of his
C. turbinatum with prototheca 13c, while his C. ceratites
(pl. xvii. fig. 24) is shown with prototheca 13 d, with tabulate
floor and vesicular sides. This latter M.-Edwards and Haime
called C. Dechent with the same form of prototheca as their
C. Bouchardit. CC. heterophyllum § appears to have a proto-
theca of the form, 13g. Goldfuss again gives a Cyatho-
phyllum helianthoides (in his pl. xx. tig. 2 e) with the same
prototheca, 13e, as that given tor the genus Ptychophyllum.
It is quite true that considerable variation in the slopes of
these flattening rims may be expected. Tor instance, in
Goldfuss’s figures of C. helianthordes, just referred to, some
have the protothcca 13¢, others wih rims even more convex
¥ Potref. Germ. pl. xvi. fig. 8a.
+ Brit. Foss. Corals, pl. 50. fig, 2.
t Pol. foss. Terr. paléozoiques, pl. x. fig. 2
§ Ibid. pl. x. fig. 1.
Ann. & Mag. N, Hist. Ser. 7. Vol, xiii. 2
18 Mr. H. M. Bernard on the
than 13. And again variations of curve are scen in the
figured section of Chonophyllem perfolcatum * with proto-
theca 130.
Thus at the very outset we find ourselves face to face with
the crux of all systematic work: What is the taxonomic
value of these slopes and curves of the rim in any individual
case? We know from Mr. Pace’s observations + that great
variability in the openness and flatness of the calicle can_be
correlated with the degree of muddiness of the water. The
sediment runs more easily off a coral with a flattened open
theca than from one with a cup-shaped theea. Then, again,
we are justified in assuming that these forms were developed
in each case by slow modifications of an originally deep pro-
totheca (age, therefore, may have something to do with the
form) ; and, lastly, we can imagine many different accidents
which would tilt or depress such rims.
Nevertheless we havea structure of fundamental importance
in the coral skeleton, and the form-variations of this structure
may justly claim to take the first taxonomic rank. But how
are we to distinguish those of importance from those which
are accidental in individual cases? The matter is further
complicated in the case of these ancient fossils, because the
transition-forms are preserved equally with those which have
passed over finally to some well-defined type. It seems
fairly clear that classification of such forms must be attempted
on wholly different lines from that still in vogue. Before
any form receives a name we should satisfy ourselves by a close
study of series that it embodies some new principle of struc-
ture. Three or four such distinct principles can be gathered
from the forms of the prototheca given in PI. I. diagram 13a-g.
In a the rim continues to show no sharp bend downwards, and
is distinet from that in which the rim tends to bend out so as
to form an open dish either as 13c or 13 /; and both these
differ from the sharper curve of the edge all round (139).
Fig. 13 A, in which the edge bends rapidly over and then either
hangs straight down or shows a tendency to curve up again,
seems to me to be very easily distinguishable from 13/, for,
even though the two might possibly pass into one another, a
smooth curve and a sharp bend are very distinct.
I propose now to leave all but one of these early variations
of the prototheca, hoping that I have said enough to claim
greater consideration for them in all future work on Paleozoic
* Brit. Foss. Corals, pl. 50. fig. 5, The section perhaps does not run
true.
+ Ann. & Mag, Nat. Hist, ser, 7, vol, vii. (1901) p. 585,
Prototheca of the Madreporaria. 19
forms. Vig. 13h, however, is of very great morpholozical
interest and demands some further attention.
In the first place, it shows a simple and very efficient
method of enabling the skeleton to stand upright. It differs
from the radicle-formation in that the lip bends over all round.
The septa which come over the lip run down on the outside
just as we know that they run down inside the radicle (see
fig. 8d). It is also obvious that the flesh of the polyp must
have clothed the outer surface of such a theca, which is no
longer the outer surface of the prototheca. To the flesh thus
hanging over Bourne’s term ‘ perisare”” may be applied, and
lower down we will compare it with, and distinguish it from,
another principle of structure which also involves the forma-
tion of a perisare. <A calicle built up of a succession of such
protothece as those now under discussion, one fitted inside
the other, as in diagram fig. 1, would have a rib-like arrange-
ment of septa running down on the outside ; but in this case
one would expect to find traces of the hanging rims appearing
irregularly one above another as whole or portions of rings
round the corallum. They would appear to be drooping or
perhaps even show a tendency to curl up again.
It is because no such epithecal rims show in the fig. 2, pl. 59,
‘ British Fossil Corals,’ that I doubt whether its prototheca
has this form (13 /) or belongs to the type I shall presently
describe as also depending upon the formation of a perisarc.
This point, then, may be left for the present. It is clear at
any rate that its true place is nowhere among the Cyatho-
phyllidee.
This form 13 is of special importance, however, for the
understanding it gives of the morphology of the Silurian
Calostylis as developed by Lindstrém.
This coral has been announced as a Paleozoic Perforate,
and this claim has had to be dealt with for the British
Museum Catalogue, the first section of which, it is proposed,
shall deal with the Perforata. As I have shown above, the
true Perforates were only possible when the prototheca was
flattened out as shown in diagram fig. 10. When thus flat-
tened the septal ridges towered up above it and free of its rim,
carrying on the skeleton by themselves alone. The thece
being constructed solely of radial plates and their synapti-
cule were necessarily porous. In Calostylis the prototheca
was not flattened out at all, but folded as shown in 13 A, and
the septa were not laminate, but appear to have been repre-
sented by a compact mass of large, irregular, rounded or
subangular nodules, arranged roughly in radial rows. These
come over the edge of the thecal told and extend down to the
Qe
20 Mr. H. M. Bernard on the
rim of the prototheca. The compact layer of septal nodules
on both the inner and outer surfaces of the calicles cause the
walls to look as if they might be perforated—as if the deep
depressions between adjacent nodules might run right through.
But this they donotdo. One of the chief puzzles of Calostylis
has been how to explain the pendent tongues of epitheca
which hang down irregularly and at intervals round the
corallum and sometimes bend even slightly outwards. There
can be only one explanation of them, and that is supplied us
as soon as we have unravelled the modifications of the proto-
theca and recognized that its rim was bent in the way shown
in this diagram. I repeat it was of importance to have this
point settled, for a Silurian Perforate was a difficulty which
the British Museum Catalogue had now to dispose of one way
or the other.
Turning from this to a somewhat kindred point which has too
long been waiting for solution, and which may be partly dealt
with in this connexion: Mr. Quelch* has raised the question as
to whether the Paleozoic Cyathophyllide are not still surviving
in the form which he has called Moseleya. Itis quite true that
we have in both cases skeletons built up of the same elements,
and at first sight similarly disposed. It has already been
pointed out by Mr. Pace that some of the suggested resem-
blances of Moseleya to a Cyathophyllum have no value, such
as, for instance, the supposed tetrameral symmetry of Moseleya.
But arguments based upon more or less similarity will not carry
us far. The relationship can only be proved or disproved by an
analysis of the principles on which the two corals are built.
It is not merely the fact that both have similar elements
somewhat similarly arranged, which is of importance, but the
principles of their respective arrangements. Now whichever
of the curves or series of curves of the rim of the prototheca
shall afterwards be decided upon as that which shall charac-
terize the genus Cyathophyllum, there is no question at all that
the special forms which Mr. Quelch relied upon (e.g. C. Stutch-
buryt and C. regium, at least as figured by Milne-Hdwards
and Haime in the ‘ British Fossil Corals’) are of the pattern
13 d with the floors tabulate and the sloping sides vesicular.
Hence unless Moseleya can show a somewhat similar arrange-
ment of tabule or vesicles, the relationship between the two
cannot be maintained. Now an examination of the available
specimens of Moseleya shows a principle of protothecal modi-
fication which, in some respects, resembles diagram 13 A; but
on closer analysis it appears to be nearer that other method
* Chall. Report, xvi, 1886, p. 110.
Prototheca of the Madreporaria. 21
of perisarcal formation referred to above, which will be de-
scribed in detail in the next section. We shall have there-
fore to postpone the further discussion of this point for a few
pages, contenting ourselves with stating that a comparison of
the protethecal specialization of Cyathophyllum with that of
Moseleya shows them to have been well nigh as wide apart as
they could possibly be.
One word before leaving these early flattenings of the
prototheca as methods adopted by the early Madreporaria for
the purpose of retaining the upright position, It is difficult
to see how, as single corals, they would be efficient for the
purpose unless the rims managed to touch the ground and
re-cement a part of the animal to the solid substratum, and
this, judging from some of the shapes assumed, does not
appear to have taken place. But what is wanted is a closer
study of the protothece and their earliest modifications. One
advantage of early flattening out they would obtain, however ;
they would grow more slowly in height, and the leverage
would not be so great. Further, if this flattening out meant
ever so small an increase in the size of the base of the proto-
theca, we can see that it might be of some value to the
coral, even though the rims did not again touch the ground.
‘The moment these flat-calicled forms begin to bud and
form colonies the advantages of the flattening become obvious,
as will be seen in another section.
IV. The Ferisarce.—One of the simplest of the really
important methods of keeping the prototheca upright was for
the soft parts to bag over all round the cup until they touched
the ground, so as to form a secondary fleshy foot. This
process differs from that shown in diagram fig. 13 A, for it in-
volves no gradual bending over of the rim of the prototheca.
I assume that the polyp simply overflowed the edge of the cup,
that it reached the ground, and even expanded somewhat over
the substratum all round the point of attachment of the
skeleton. Since the under surface of this overhanging flesh
is a continuation of that which secreted the prototheca, it
might be expected not only to secrete a layer over the outer
face of the cup, but also to deposit a continuation of that layer
where it touches the ground. ‘This latter might be thickened
to form a solid pedestal, in which the tip of the prototheca
would be firmly fixed. ‘The fleshy foot secondarily formed in
the way described may have taken almost any shape, even
sending out radial prolongations or embracing the round
stems of weeds, in which cases the solid pedestals which it
secretes would encircle such stems, fixing the corals firmly.
When once fixed the coral may continue to grow in height
22 Mr. H. M, Bernard on the
and size without fear of falling over. If the rise in height is
slow the soft parts hanging all round down to the ground
may go on thickening the wall, and especially the base,
almost indefinitely, so as to keep the corallite nearly cylin-
drical. In such cases the septal ridges on the inner face of
the cup may be continued over the edge as ridges (coste) or
as rows of (costal) spines down the outside. On the other
hand, as soon as the base of the prototheca is sufficiently
firmly fixed the corallite may grow rapidly in height as well
us in width, and in so doing may drag the soft parts away
from contact with the ground. ‘The latter will then persist as
the typical ‘ edge-cone” or “ Randplatte” round the mouth
of the corallite. The withdrawal of the parts that thickened
the base while the coral grows in size leads to the latter
being turbinate.
Irom this point of view the typical “‘edge-zone”’ is in
reality a vestigial structure ; it is the remains of the perisare *
which in the young stage formed the secondary fleshy foot.
But even as such it may continue to fulfil some useful
function. It will always continue to leave a layer of skeletal
matter on the outer face of the prototheca, thus increasing the
thickness and strength of the latter, and it will continue to
form costal (=septal) ridges or spines. In Galavea advan-
tage is taken of its gradual withdrawat from contact with the
ground to secrete horizontal or arched filins round the base of
each calicle. In this way the corallites of a Galaxea colony
are embedded in and supported by an increasingly thick
layer of irregular filmy vesicular tissue f.
We are now in a position to reconcile our statement that
the epitheca, as usually seen in adult corals, is the rim of the
protothecal cup perhaps indefinitely expanded, with the
appearances which have led to the text-book statement
* I suggest this distinction between Bourne’s “ perisarc” and the
“ edge-zone” of Miss Ogilvie; the edge-zone is the vestigial perisare. It
is important not to confuse the perisare which hangs over the solid edge
of the prototheca with the sides of the polyp of a perforate coral in which
the prototheca has been flattened down and the septa alone form a
secondary internal theca, and no bagging over of soft parts ever took
place.
t+ There is in the Natural History Museum a specimen showing a
group of “ Caryophyllia clavus” growing on a piece of a telegraph-cable
from the Caribbean Sea (700 fath.). The individuals are near together
and their perisarcs have covered the intervening spaces with a chalky
film. Here and there in the angles made by the corallites with the sub-
stratum the film is raised and slopes outward and downward from the
sides of the coral. It is this kind of free film formation which has been
specialized in Galavea.
Prototheca of the Madreporaria. 23
that the epitheca is that part of the skeleton secreted by the
edge-zone and left on the sides of the coral as it (the edge-
zone) is drawn up with the growth of the coral. This secretion
may show periodical wrinkles or thickenings if the withdrawal
is intermittent; and it is also clearly epithecal, inasmuch as,
morphologically, it must be regarded as a doubling over of
the rim of the prototheca, as can be gathered from the diagram
(fig. 14). But this secretion is only one of many, and,
moreover, one of the most highly specialized, modifications
of the rim of the epithecal cup. Hence while it is quite
correct to call it epitheca, it is quite incorrect to define epitheca
in terms of this single specialization of it.
It is also clear that if the term “ eutheca” is applied to
such cups as those shown in diagrams fies. 1, 2, 4, and 5, in
which the lip of the prototheca grows straight on, we want
some other term to designate a cup in which the bagging over
of the soft parts has practically doubled back the edge of the
cup, so that the fold adheres to its sides (see fiz. 14). But I
would suggest that the simple unmodified theca should be
called prototheca, while the term eutheca would be more aptly
applied to the theea which has been secondarily attached by
a solid pedestal, thickened by the extra matter secreted on its
outside, and strengthened and armed by ribs and spines. We
might call the wall of Zaphrentis, Streptelasma, &c. (diagrams
figs. 1-4) “continuously protothecate’”’ and that of Monéli-
valtia (diagram fig. 3), or at least of those specimens in
which the septa can be seen between the edges of successive
saucers, discontinuously protothecate.
But although this eutheca, with the meaning just suggested,
is due morphologically to a doubling of the wall of the proto-
theca by the secretion of a layer on the outside of the cup, it
can hardly be described as due to a bending over of its rim.
I conceive of it rather as due to the rapid bagging over of
the soft parts, without at the moment any actual continuous
growth of the rim. A true bending over would have been a
growth process of the rim itself (see fig. 13g). I imagine
that only when the soft parts had acquired their new position
on the outside of the cup that they commenced secreting the
external layer, which is nevertheless strictly a continuance of
the rim down the outside and into the basal pedestal.
This explanation of the morphology and origin of the edge-
zone throws an interesting light upon a very specialized and
morphologically puzzling group, viz. the small highly sculp-
tured free Turbinolide. ‘heir origin can now be understood
from diagram fig. 14, if we suppose that the powers of secreting
24 Mr. H. M. Bernard on the
carbonate of lime were for some reason restricted, perhaps
locally *. In that case the outside fleshy foot might fail to
secrete a solid pedestal, and then if, perhaps owing to the move-
ments of the animal itself, the prototheca became detached
from the substratum, it would be completely enveloped by the
polyp and become a small internal cup-shaped skeleton. The
ribs or spines coming over the edge of the cup could then
run right down to the extreme tip of the original prototheca,
as they do in typical members of the genus. If this origin is
correct, the genus Turbinolia will have to be regarded as an
extreme specialization of the “ Huthecate corals,” and can
hardly, as it now does, give its name to a family.
It is evident then that a considerable reshuffling of the
Milne-Edwards classification is required. For instance, as
has already been pointed out by Bourne, the “ Turbinolide ”
can no longer contain such purely protothecate forms as
Flabellum and Rhizotrochus, while the Euthecate corals will
have to include such forms as Galavea, Huphyllia, and Mussa,
which were placed among the Astreide by Milne-Edwards
and Haime. Turbiénolva itself will be a specialized offshoot of
the Euthecate corals. It would, however, be premature to
found such morphological divisionsas Protothecata, Kuthecata,
for it might be discovered, for instance, that the method of
forming a perisarcal foot round the larval prototheca has been
adopted more than once by different types of coral. Indeed,
we seem already to have discovered two ways, viz. that
shown in fig. 14 and that found in the Paleozoic Calostylis
(fig. 13%).
And this brings me back again to the much discussed genus
Moseleya, already referred to as that which Mr. Quelch,
working on a single specimen, took to be a Cyathophyllid.
Fortunately Mr, Pace was able to bring more specimens of
Moseleya, and I have found two others in the great collection
made by Mr. W. Saville-Kent on the Great Barrier Reef. All
these specimens are Lithophyllic. The only difference that
I can detect between them and the ‘ Cuallenger’ specimen
lies in the fact that the latter has flatter and more open
calicles. This, as Mr. Pace suggests t, may be merely an
adaptation to the mud which we gather is present in the parts
where the ‘ Challenger’ specimen was obtained. Examination
of the specimens with a view to discover what was the
principle of protothecal modification overlying them reveals
the type of structure shown in the diagram fig. 15. It is
* They are plentiful in the Barton Clays.
¥ Ann. & Mag. Nat. Hist. ser. 7, vol. vil. (1901) p. 385.
Prototheca of the Madreporaria. 25
essentially the same as that shown in fig. 14, but the proto-
theea was shallow and open and the soft parts had bagged
over the low walls on to the ground, doubling them as shown
in the figure. Large wing-like septa come over the wall and
also reach to the ground or to the rim of the epitheca all
round outside. Between these flange-like septa, as they grow
upward and outward, the polyps leave one basal secretion
atter another, so that both inside the cup and outside it there
is an increasing thickness of vesicular tissue. In the diagram
(fig. 15) the lines are drawn as so many distinct tabule.
But it would hardly be expected that the successive detach-
ments of the polyp would take place simultaneously within
each interseptal loculus, right fromm the centre of the calicle
over the edge of the theca down to the ground. But as
dissepiments are only portions of tabule, the diagram is the
best way of illustrating the facts. ‘This type of. structure, in
which the vesicular tissue not only rises between the septa
within the calicle, but also thickens the column between the
coste outside it, is that which lies at the base of Lithophyllia.
It is true that emphasis has not hitherto been laid upon this
point, for the simple reason that the prototheca had first to
be discovered. Milne-Mdwards and Haime merely remark
that dissepimental tissue is very abundant, while their classing
Mussa with Lithophyllia shows clearly indeed that the
arrangement of the dissepimental tissue had not been analyzed.
On the other hand Knorr, to whose figure among others
Milne-Edwards and Haime refer as a type of L. ducera,
mentioned the “stony films round the foot” and deserivcd
the impression made upon him by the words “new crowns
continually covered up the old ones.” ‘Tle meaning of this
otherwise enigmatical saying is quite clear when we glance
at the diagram (fig. 15) here given. We conclude, then,
that there is no generic difference between J/oszleya and
Lithophyllia and that the genus J/ose/eya is superfluous. At
the same time it is due to Mr. Quelch to point out, (1) that
the analysis of the essential structure of Moseleya was hardly
to be discovered from the single specimen at fis disposal at
the time, and (2) if it had been, there was no existing descrip-
tion of Lithophyllia which would greatly have helped him,
‘The calicle of which he made a section was old, very much
flattened, and somewhat distorted, and with the tissue on its
exposed side largely killed down, ‘This latter point is of
gicat importance, for it is the structure of the sides of the
column which is essential to a correct diagnosis. Once,
however, the clue is given, which is supplied in abundance
by. the new specimens, the structure is easy to comprehend.
26 Mr. H. M. Bernard on the
With the striking superficial resemblance to Cyathophyllide
to mislead him, it is no wonder that Mr. Quelch was misled.
Nor do I see how his claim could have been disproved without
a clear understanding of the position of the prototheca in
coral morphology.
While on this subject I may point out that Mr. Quelch’s
figure (/, c. pl. xii. no. 5) of a small calicle of JMoseleya
showing marked tetrameral symmetry is seen on the actual
specimen to have been distorted by too close contact with the
shell of a mollusk much larger than itself. Its internal
arrangement is not quite normal. Mr. Pace has presented
the Museum with over a dozen specimens, most of them
single forms in all stages of growth, and not one shows any
such striking tetrameral arrangement. On this subject of
tetrameral symmetry in the so-called “ Rugose” division of
the Madreporaria I would refer the reader to what is said
above (p. 11).
Whether, after all, the subsequent classification of the
Lithophyllide will ultimately admit of the existence of a
genus Moseleya among them [ cannot say. In this paper I
am only concerned in showing that it has no place among
the Cyathophyllide. The latter are characterized by extreme
simplicity of protothecal modification, the Lithophyllide by
great complexity ; they are at opposite ends of the evolution
of the coral skeleton,
Before closing this section I should like to refer once more
to the difference between the principles of modifying the
prototheca shown in diagram fig. 13 A and diagram fig. 15.
In both the soft parts bag over and reach the ground, but in
the former the lip grows with the growing of the soft parts
and its bend isa true bend. In fig. 15 the soft parts seem
to overflow the edge of the cup too rapidly actually to bend
the edge. Quly aiter they have taken up their new position
do they secrete a layer on the outer side of the cup, and this
layer is practically the homologue of the bent-down edge
shown in fig. 13 4. ‘The two methods are thus clearly
distinct, but it is not always easy to say whether a particular
case belongs to the one or to the other. *or instance, in those
specimens of Lithophyllie in the Museum which have the
corallites crowded together and forming pseudo-colonies, it is
trequently noted that where the interseptal loculi of adjacent
corals run into one another the dissepiments are everywhere
arched, suggesting an open bend of the theeal lip, such as is
shown in the diagram fig. 13 A, or even more resembling the
bend of fig. 18 g, or even of 18f. But in the specimens with
single corallites the actual lip of the theca is mostly a solid plate
Prototheca of the Madreporaria, 27
like those shown in diagrams figs. 14 or 15, and from it the
dissepiments slope away on the one side into and across the
calicle, and on the other down to the substratum. But it is
doubtful whether an actual section of the wall would show
that structure so straight and continuous as it is shown
diagrammatically in the figure (15), and it is quite certain
that the tabula would not be so regular and complete.
It was some such case as that just referred to (? a specimen
of Acanthastrea), in which vesicular arched walls separated
ealicle from calicle, that inspired the diagram given by me on
pl. xxxii. tig. 10 in vol. xxvi. of the ‘ Journal of the Linnean
Society of London.’ I am not yet, however, prepared to
answer the question as to which of the two methods of edge-
zone formation we have just been comparing—that of fig. 13h
or of fig, 15—the actual case was due. For, as we have
just seen, the Lithophyllie show that the smooth, arched,
vesicular dissepimental wall might be a secondary modifica-
tion, and due to colony formation, of the true edge-zone
formation of fig. 14, which is the subject of this section.
V. Early Budding and Colony Formation.—In vol. iv. of
the ‘ British Museum Madreporaria,’ Introduction, p. 23, I
suggested a restricted use of the word “ astreiform,” viz.
to colonies of calicles all reaching to the same height and
without any apparent tendency to grow and bud independently.
The true astreiform colony is therefore that built up by a
ealicle which is by habit low and whose buds spread laterally
over the substratum all round the parent. ‘The group
Astraide as now understood consequently cannot be a natural
one. It appears to me that we may have astreiform colonies
of corals whose protothecee are modified upon very different
plans. And it is on these modifications of this fundamental
clement that the ultimate classifteation will have to be based.
We might expect, then, a great development of astraiform
colonies among the Paleozoic corals from the forms in which
the prototheca was early flattened out in the ways described.
We inight also expect that it would be those methods of
flattening out which were from the first symmetrical, because
if the parent had acquired its flattening as a secondary
matter, after having perhaps at one time fallen over, it could
hardly be expected that the buds would appear with the
necessary flattened symmetry straight away, although in some
of the Astreid forms with very large calicles this must
apparently have taken place.
While I think these conclusions are perfectly justifiable,
we learn from the researches of Lindstrém that one great
group of Paleozoic astreiform corals with very small calicles,
28 _ Mr. H. M. Bernard on the
e. g. the genus Helvolites, developed from a prototheca which
had fallen over. From Lindstrém’s figures * we gather that
the lip which touched the ground expanded as a flattened
epitheca over the substratuin, and buds appeared at intervals
upon it. Especially characteristic are the various wrinklings
and ridges which appear on the upper face of the epitheca
between the buds. As the living layers were periodically de-
tached from and rose above this epitheca they secreted tabulate
floors, which repeated its wrinkles and foldings. In this way
the structure seen in the section typical of the Heliolitide was
produced. Through the tabulate lamine which form the
bulk of the coral the calicles run as tubes, while smaller tubes
also appear in many cases in the intervening tabulate tissue.
‘These smaller tubes receive their explanation as the continua-
tion of the folds or wrinkles already mentioned through the
whole series of tabule. Such folds or wrinkles would run as
naturally through a series of tabule as the septa run appa-
rently continuously through the tabule of Montlivaltia, as
already explained in fig, 3 and p. 8.
If, however, we had had no knowledge of the origin of
Jleliolites, we should have assumed that it had been built up
of calicles with the form shown in fig. 13,7. And, indeed,
this is the form which the calicles of the adult colony assume,
but it is not arrived at by a symmetrical outward folding of
the rim of the prototheca, but indirectly from a parent the
unmodified prototheca of which fell over in the way already
described. We owe the small size of the calicle of //eléolites
to this fact.
The chief difference between the Paleozoic and Recent
astrxiform corals is due entirely to the more recent development
of the radial or septal, as compared with the concentric, proto-
thecal foldings. In Paleozoic times the former were not very
pronounced, so that the flattened or curved sides of the proto-
thecal cups with their tabulate floors formed the most charac-
teristic portion of the skeleton. ‘The cup was, however,
never quite flattened out, there is always the remains of the
bend where the lip first turned over. These bends frequently
form ring-folds (see fig. 137), which become the walls of the
fosse, while tabule form not only the floors of these fossa,
but also the areas which intervene between the fossa. ‘These
areas are variously sculptured with radial septa, and when
the respective areas of the individual ecalicles are not marked
off from one another, the septa of one may run into the septa
* See K. Sv, Vet.-Akad. Handl. xxxii. (1899), pl. i, figs. 25-28, -Com-
pare the case of Paleocyclus referred to above.
Prototheca of the Madreporaria. 29
of those around it, as, for instance, in Darwinia and
Phillipsastrea,
On turning to modern Astreide, we find that the tabulate
character of the Paleozoic corals has become obscured, on
the other hand the septa have become prominent. ‘These
conspicuous radial folds of the prototheca make it difficult to
discern the exact character of the concentric foldings of the
protothecal wall.
I would suggest that, as a rule, the rising of the radial
septal folds has also raised the concentric rim-folds. We
might diagrammatically express it by imagining a calicle
like that in figure 13 7 becoming changed into the form
shown in fig. 16, which represents a calicle with high double
walls, and on each side of it asmaller bud. We may assume
that the tall ring-fold has been formed at the expense of the
earlier horizontal tabulate area round the fossa. It is im-
possible here to attempt any review of the many Astraid
forms, but, speaking roughly, they are built of groups of low
ealicles with the protothecee modified in this way. ‘The
difference between this and that shown in diagram fig. 14 is
that the calicle is shallower and more open.
Without professing any intimate knowledge, I am inclined
to believe that most of the different forms now included
among the modern Astreeidee may be referred to variations :—
(1) In the distances of the corallites from one another:
(a) they may be wide apart, as in Orbicella, Solenastrea,
Echinopora, &c.; (6) they may be close together, Fawa,
Diploria, &c.; (c) they may be so close that the outer wall
of the parent supplies the inner wall of the bud, Prionastrea,
Goniastrea, Leptastrea*, &c.; (d) even these single division-
walls may be incomplete, Hydnophora.
(2) In the ways the intercalicinal valleys are filled up.
(3) In the characters of the septa and in the way in which
they come over the edges of the fossa and are distributed on
the surface of the intervening tissue.
Concluding Notes on the Terminology of the Walls.
A wall built by a direct continuation of the edge of the
prototheca should, I think, be called protothecayt. These
* The Paleozoic Michelinia might be regarded as the morphological
equivalent of these forms before the development of septa disguised the
protothecal cups.
+ The term epitheca may be retained in its usual sense, and be under-
stood to refer to all traces of the primitive undifferentiated protothecal
wall and rim, even though they haye lost all signs of haying been once
parts or expansions of a cup.
30 Mr. Il. M. Bernard on the
primitive protcthecal walls, recognized by Miss Ogilvie as
equivalent to epitheca, have been hitherto called eutheca.
But proto- is a more appropriate affix to express primitive
simplicity than ew-, which better denotes some special excel-
lence. Hence I propose, once more, that eutheca be applied
to those walls which have been thickened, ornamented outside,
and cemented firmly to the substratum in the way described
above (p. 22) and illustrated in diagrams figs. 13 A, 14,
and 15.
We now come to the term “ pseudotheca”’ of Heider. This
is applied to cases in which the septa are so crowded together
that they fuse alone lines which together constitute a fairly
symmetrical solid thecal ring. The parts of the septa within
this ring are septa proper and the parts without are costa.
Now I cannot help doubting whether this differs in any
respect from the eutheca, for it is obvious that a eutheca, as
here understood, over which the septa ran close together,
would give exactly the same result.
The suggestion that this wall is built wholly of fused septa
does not take the possibility of a ring-fold into account. But
from the review of coral morpholozy here set out it would
appear that the ring-fold was a more primitive structure than
the radial septa. I*urther, it is really impossible in a matter
of such complicated folds to say how much at their points of
crossing belongs to the radial and how mush to the con-
centric elements.
That the concentric element plays a part we gather from
the fact that dis$epiments frequently slope up the interseptal
loculi just as if, had there been space enough, they would
mount over the walls. This giving off of dissepiments
means that the basal floor shares in the formation of the wall.
What is usually called pseudotheca, then, is to my mind
simply a modification of the eutheca as here understood, and
the word, if retained at all, should have a new significance.
My own proposal is to apply it in the sense of Ortmann’s
“athecalia” *, This term was suggested by that author for
the Perforata in which the protothecal cup, being entirely
flattened out, a new secondary theca rises up formed entirely
out of septa with their synapticular junctions. Now it is
obvious that no part of the old protothecal rim is found in
this new septate thecal wall, and to mark the total distinction
between this and all the wall-formations made by folds of
the true lip of the prototheca, it might well be called pseudo-
theca.
* Zool, Jahrb. (Syst, Abth.) iv. 1889, p, 493,
Prototheca of the Madreporaria. 31
The term “ athecalia ” of Ortmann, it may be remarked, has
not been very well received, for it is certainly not true that
the corallites, say, of Madrepora have no thece. The very
opposite is the case; the thecee are most pronounced. What
we want to express is that these thece are morphologically
distinct from the original thecve of the Madreporaria, and no
better term could be employed than that here suggested—
pseudotheca.
Tam aware that a long critique of the views and suggestions
of other workers on the subject of the wall should be offered
before proposing a revision. But I have the excuse that the
revision of the terminology here suggested rests upon a
somewhat far-reaching revision of the skeleton. A closer
comparison of the terminologies would involve a closer com-
parison and criticism of the views on the wall-structure of each
different author, some of which are, I confess, not always
clear tome. Indeed, we seem to have had enough of detailed
and complicated discussion. The great want is some simple
working hypothesis which will enable us to coordinate the
facts.
My own work has convinced me that some order appears
out of the chaos if we recognize the prototheca and give it
the important place in the morphology of the coral skeleton
here all too briefly sketched.
In conclusion, I should like to emphasize the fact that this
paper is intentionally devoted to the prototheca and its con-
centric modifications—that is, to those modifications which
alter its cup-shape concentrically. Only occasionally and
where necessary reference has been made to the great and
complicated system of radial wall-folds which are the most
characteristic structures of the stony corals. These have,
however, claimed the attention of workers too exclusively in
the past. We shall only be able to obtain a true insight into
the evolution of the coral skeleton when we understand both
systems of modification—the more primitive concentric and
the Jater radial—and can trace out their influences on one
another. It is to me a matter of sincere regret that this
paper was not published prior to Miss Ogilvie’s comprehensive
and patient treatise on the septa, for her valuable observations
would then, I am convinced, have admitted of more precise
and coherent treatment.
EXPLANATION OF PLATE I.
vg. 1, The three earliest growth-periods of a primitive Madreporarian.
The thick basal part is the prototheca (sens, strict.), see fie. 2.
Rig, “2:
Fig. 3.
Tig. 4
Fig. 5.
Fig. 6.
EGG. 1.
Fig. 8
TGs iO
Fig. 12.
On the Prototheca of the Madreporaria.
The curved line a represents the secretion of the basal skin
after it has been dragged (?) out of the prototheca by the
growth of the walls in height; 6 represents the secretion
formed by the skin after it has become detached from a.
The same regarded hypothetically as three separate cups, the
lowest thick-walled cup being the prototheca (sens. strict.) ; in
it cup aaa is inserted, and cup 660 in aaa.
A diagram to explain the morphology of Montlivaltia. The
early cups rapidly expand and eventually become a series of
saucers, ee... supported above one another by the septal folds
which run continuously upwards. On the right half of the
figure the upper part is in section, showing the tabulate floor
and the irregularly bent-up rim. On the left half these rims
are shown from the outside as irregular bands of epitheca
running round the coral.
. An early stage like that of fig. 1, but, having fallen over and
resecreted itself at a, it bends upwards again. The bagging
of the detached basal skins will take the shapes shown, and
the fossula iu the bases of the cups will be on the convex or
dorsal side of the curved skeleton.
A diagram to show how, if the prototheca proper was wide-
mouthed when it fell over, the fossula will come over to the
ventral or concave side. dis again the spot where the coral
secretes a new attachment.
The diagrammatic representation of the arrangement of the
septa in the so-called Yetracorallia, It receives a simple
explanation as due to the necessary rearrangement of the septa
in a coral which fell over and was bending up again. See text,
ps wl:
. Diagram to illustrate the method of budding of a prone proto-
theca and the subsequent bending upwards of parent aud buds
which might give rise to such a form as TZalysites.
. Two figures of radicle-formation, after Lacaze-Duthiers.
. Diagram to illustrate the one-sided bend-over of the prototheca
such as it is suggested would give rise to the Zaphrentis
gigantea of Milne-Edwards and Haime. See text, p. 14.
. Diagram to explain the early flattening out of the prototheca in
the Perforata. The rim of the cup creeps outwards all
round, generally with successive slight bendings up and then
down again.
. Diagram of the early stages in Pale@ocyclus. The prototheca
proper seems to have fallen over and then suddenly to have
widened out, the repetition of this is still more widened out,
and so on. What appears to have been a wrinkled basal
epitheca is not a continuous growth like that in fig. 10, but a
repetition of so many separate protothecal rims.
Diagram of the early stage of Cyclolites. The prototheca is
nearly flattened out, but it is still repeated continually, only
instead of the secretions of the successively detached skins
forming continuous tabule, they are broken up into vesicular
dissepiments. Here also what appears to be the wrinkled
epithecal floor is in reality a concentric series of separate rims,
Figs. 18.a-g. Various forms assumed by the protothece in Paleozoic
corals, all in the direction of becoming flattened out. The
developmental transitional stages between the deep proto-
theca and these adult forms haye still in many cases to be
worked out. j
On some Parasitic Bees. 33
Figs. 13h and 7. Two types of foldings of the wall of the prototheca—
h, seen in Calostylis; 7, common in early astreeiform colonies,
e. g. Heliolites.
Fig. 14. Diagram to show the overflow of the prototheca by soft parts
which bag all round down to the ground and form a new
fleshy foot. This secretes a pedestal which can fix the proto-
theca firmly to the substratum and doubles the thickness of
the protothecal wall. This, it is suggested, should be called
the eutheca.
Fig. 15. Diagrammatic section of a Lithophyllia. Large wing-like septa
radiate out over the wall, and dissepiments are formed on
both sides of it; within the calicle they slope inwards, on its
outer side they bend down and thicken the column with
vesicular tissue between the coste. Mr. Quelch’s genus
Moseleya is built on this plan, and cannot therefore be a
Cyathophyllid with prototheca modified on one of the simpler
plans shown in figs. 13 a-f.
Fig. 16. A diagrara to illustrate the principle of structure characterizing
the modern Astrzeidee: 1 is the central parent calicle with
the prototheca modified somewhat as in fig. 14; 2, 2 represent
buds from the lateral edges, the budding thus resulting in
the production of an astreiform colony.
Il.—Some Parasitic Bees. By T. D. A. CocKERELL.
Celioxys ribis, var. Kincaidi, n. var.
? .—Length 11-13 millim., the difference in size partly
dependent on the extension or retraction of the apical part of
the abdomen.
Similar in all structural characters to C. ribis, but the
pubescence of the head and thorax is ochreous, the basal part
of the third abdominal segment is more sparsely punctured,
and the apical dorsal plate has the apex beyond the slight
lateral constriction a little more produced. There are distinct
and conspicuous transverse grooves across the middle of the
second and third abdominal segments, but not on the fourth
or fifth. Tibial spurs black.
Hab. Olympia, Washington State, June 9 to 24, 1895,
June 26, 1896, five females (7. Kincaid).
This is the first Celioxys recorded from the north-west.
It is quite different from ridis in appearance, but structurally
it is almost the same, having the same sculpture on the
penultimate ventral segment, &c. A male collected by
Mr. Kincaid at Olympia, June 18, 1895, is presumed to
belong to C. ribis Kincaidi, though the pubescence (especially
on the face) is white. This male almost exactly agrees with
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 3
34 Mr. T. D. A. Cockerell on
C. sodalis, Cresson, though the lateral teeth of the scutellum,
while obtuse, are not short; the apical margins of the wings
are only slightly dusky. The tibial spurs are black, and the
fifth abdominal segment has no lateral teeth, though there are
minute nodules. The lateral teeth of the sixth segment are
long. The upper apical teeth are flattened and rounded.
The spines on the anterior coxe are large and blunt. It is
to be remarked that while C. rzbi’s was described from a
locality in the upper austral zone, it is also an inhabitant of
the boreal, and probably goes far north of New Mexico. On
June 29, 1902, my wife took females of (C. ribis and
C. Portere at flowers of Frasera at Beulah, New Mexico, in
the Canadian zone.
The exact relationship of C. sodalis to ribis and Kincaidi
will not be determined until the male of the first-mentioned
is discovered. The localities given for sodal’s are New York
and Colorado; New York, being first mentioned, may be
considered the type locality. I rather expect that ridis and
sodalis will prove to be one species.
EPeo.us, Latr. (sens. lat.).
Females.
Fifth ventral segment of abdomen
strongly concave in lateral view ; fifth
dorsal segment truncate; size large.. 1.
Fifth ventral segment not so ........ 2.
Ly bege black. o1ih: ie citele ae sce npeees Triepeolus concavus (Cress. ).
begs ferrupinouss stn es come eres Triepeolus penicilliferus
2. Fifth dorsal segment with only a diffe- [(Brues).
rentiated apical lunule; small species.
(Zipeotiay™ ee cee ee eee 3.
Fifth dorsal segment with a large diffe-
rentiated area; large species. (7ri-
ENCOUUS) alae at isteren cei e + aR 6.
3. Front with a tubercle on each side;
Scutellum reds. wi ewtewetss che ela bifasciatus, Cress.
Front simple; scutellum black or
faintly reddish \<.c\0..4 oocke oe beteke 4.
4, First abdominal segment hairy all over;
antenne red, suffused with blackish ;
tibial spursiclear vedi.) h. fn. swat 2 erucis, Ckll.
First abdominal segment with a black
hairless area; antennee black, with
little, af amy, ared Scr ei pete oe oie ete 5.
5. Hind tibial spurs black ; two submar-
ginal cells; antennze entirely black;
lower half of pleura hairless ...... Phileremus americanus,
Hind tibial spurs clear red; three sub- (Cresson,
marginal cells; second and third
some Parasitic Bees. 35
antennal joints largely red; lower
half of pleura covered with hair ,
Gr legs black... ai) avalon Riana te
Legs OO Peseckis ax scp tete« oes, anecaiataas
7. Larger; black area on first segment
10.
D3 bs
ou
~y
narrow, % e. not much produced
laterally SARA SEN. eAG Ms Ward as ode ce
Smaller; black area on first segment
SCN DEO fn oh eA eaio a aPa ouni sa a8, nis
. Scutellar teeth long and_ sharply
pointed, at least par tly red; dark area
on disk of first segment very small. .
Scutellar teeth shorter, entirely black .
. Larger; mesothorax mainly red
Smaller ; ; mesothorax black .....,..
Area on first segment a broad trans-
verse: band’ 3479.0 ee apa.
Area on first segment small, not pro-
duced laterally ; SIZE) LAT BON ec ara oie
Tegule clear light red; * mesothorax
with an anterior patch, not two dis-
MINE SEELpES Sesh ee to. oe
Tegule dark reddish to dark fuscous ;
mesothorax with two distinct stripes.
. Larger; labrum entirely black ..... :
Smaller; labrum with two red spots. .
Males.
Abdomen with eight elub-shaped sci
AMVATICS) spate ovoe SEG eee Fe
Abdomen not so marked..........++
. Markings of abdomen orange, white on
sixth segment Aho Gaeghecoine
Markings ~ of abdomen white or " pale
CREAM CO LOND sth aces ajstaieanitsin oleh ee
. Mark on first abdominal segment semi-
DIRT eo ahokaheh ols & 6 + Gre os oe
Mark on first abdominal segment 2
transverse band...... Sererainpe sister ais
elees black. ssc. Beha Nitec oe ater eats
ISAS TCR Ap Bribes Pl Mh oem svere 6 ahd lode veh te
. Bands on second to fourth segments
interrupted in middle line; size
Rielle femora, DAC Kc. a4 veges v0 oe tp
Bands on third and fourth segments, at
least, entire; hind femora, at least,
TTL gic eotple ee Oe ee pels Soins
. Lower part of pleura bare ..........
Lower part of pleura covered with hair.
a luarger; tegule clear red © ...5-00a0-
Smaller ; ; tegule darkened ....,.....
. Anterior femora red ; abdominal mark-
inesevenurcms sate. etl. oe
Anterior femora black; abdominal
markings cream-colour; antenne
blackeesecsrpees SF ee 6 AS Rae
bewahensis, Chl.
nevadensis, Cress.
donatus, Smith,
2!
10.
pimarum, Ckll,
mesille, Ckll.
11.
tevanus, Cress.
oecidentalis, Cress.
12.
heliantht, Rob., var.
helianthi, Rob,
verbesine, Ckll.
nautlanus, Ckll,
5)
ade
3.
concolor, Rob.
lunatus, Say.
olympiellus, Ckll.
5.
6.
ie
occidentalis, Cress.
helianthi, vay. arizonensts,
[Ck],
tsocome, Ckll.
Cressont, var. frasere, Ckll,
*
36 Mr. T. D. A. Cockerell on
Triepeolus nautlanus, sp. 0.
g .—Length 9$-11 millim.
Agreeing with 7. lunatus and JT. concolor except as
follows :—Light markings of thoracic dorsum, and particu-
larly of dorsal segments of abdomen, light orange ; sixth
dorsal segment with the pubescence entirely silvery white,
in strong contrast with the orange of the other segments; the
extreme sides of the second to fitth segments are touched with
silvery white, which is most conspicuous on the fifth; the
bands on the second and third ventral segments are silvery
white, the erect curved hairs on the fourth and fifth being
fuscous ; the pubescence of the face is entirely silvery (not
golden at the sides as in 7. flavofasctatus) ; the lower part of
the pleura is hairy, with an ill-defined bare central area ;
mandibles with a dull red spot in middle of outer side; an-
tenne black, first joint of flagellum red beneath ; tibies and
tarsi red, spurs on middle and hind tibie black; femora
black, reddened at apex, and the middle femora sometimes
red beneath ; the tibiz vary to black, but the tarsi in such
specimens remain red.
Hab. Vicinity of San Rafael, Rio Nautla, State of Vera
Cruz, Mexico (C. H. I’. Townsend). The dates are March 13
and April 7; it occurs at flowers of plant no. 1 of ‘Townsend’s
collection, which is a species of Compositee.
The insect is a tropical representative of 7’. dunatus, appa-
rently constant in its bright colours. It is possible that
T. nautlanus may prove to be the male of the species
described by Cresson from the female as Hpeolus totonacus,
Triepeolus nevadensis (Cresson).
Albuquerque, New Mexico, Sept. 15.
Recorded erroneously in Bull. Denison Lab. as Epeolus
remigatus (p.73) and EH. rebustus (p. 61). It is easily known
from robustus by the prominence between the antenne.
E. robustus was described from New Mexico, but I have not
met with it.
Triepeolus pimarum and 7’. mesille, spp. nn.
The females of these two species agree in the following
characters :— Light markings of thorax and abdomen cream-
colour; first abdominal segment with only a very small
median black mark; second to fourth segments with broad
even bands, that on second with no anterior lateral processes ;
labrum, greater part of mandibles (at least), and first three
some Parasitic Bees, 37
joints of antenne and base of fourth red; considerable white
hair about base of antenne (not soin 7’. bardus), but clypeus
and adjacent sides of face hairless ; clypeus and face extremely
closely but very distinctly punctured ; pleura very strongly
punctured ; tubercles red ; hind border of prothorax densely
pubescent; mesothorax extremely densely punctured, not
hairy, but having a sort of mealy appearance; two short
anterior stripes of pubescence (slender and very weak in
mesille) ; scutellum not or hardly at all bilobed, its lateral
teeth very long and pointed; only the margins of pleura
hairy ; tegule apricot-colour ; legs red, some blackish suffused
markings on middle and hind femora; hind tibial spurs dark ;
hair, on inner side of basal joint of hind tarsi orange; abdo-
men extremely closely punctured ; fifth segment without a
band, convex, with fine silvery pubescence, and with a
quadrate minutely roughened red area; apical plate red,
punctured, sharply truncate ; ventral surface of abdomen not
banded, but pruinose, with minute white pubescence. They
differ as follows :—
T. pimarum.
Larger, length about 123 millim.
Clypeus red.
Mesothorax red, with a broad
median black band.
Scutellum and pleura (except an
oblique black band) red.
Teeth of scutellum curved at
ends.
Apical plate of abdomen not or |
hardly keeled.
Punctures at sides of second and
third ventral segments of abdomen
not conspicuously different,
Wings quite dark, nervures
piceous.
Three submarginal cells.
T. mesille.
Smaller, length 11 millim.
Clypeus black, with anterior
margin red,
Mesothorax entirely black.
Scutellum black, the ends of the
teeth red; pleura black, with a
faint reddish spot.
Teeth of scutellum straight,
Apical plate of abdomen keeled.
Punctures at sides of second and
third ventral segments very diffe-
rent, those of second being much
larger and less dense.
Wings not so dark, neryures
fuscous.
Nervure between second and
third submarginal cells usually in-
complete.
T. pimarum was found by myself at Alhambra, Salt River
Valley, Arizona, in the autumn of 1899, at flowers of Verbe-
sina encelioides.
Of T’. mesille I collected a number of
specimens at Mesilla, New Mexico, Sept. 24.
Yor a long
time I have had the latter species labelled with doubt
T. bardus, Cresson, but I believe it to be distinct, though
closely allied.
bardus are incurved.
According to Mr. Brues the scutellar teeth of
38 Mr. T. D. A. Cockerell on
Triepeolus donatus (Smith).
A female in the National Museum, from San Bernardino
County, California, October (Cogullett), is referred here, as
it agrees in every particular with the descriptions of donatus
by Smith and Cresson, except that the pubescence of the
abdomen is identical in colour with that of TZ’. concolor. It is
to be remarked that 7’. superbus (Provancher) has nearly the
same characters ; but its pubescence is pale yellow and the
markings of the abdomen appear to be different.
Triepeolus isocome, sp. 0.
The male was taken at Albuquerque, New Mexico, Sept. 16,
at flowers of Isocoma Wrightit, and was recorded in Bull.
Denison Lab. xi. p. 78, as Epeolus occidentalis. It is
certainly a distinct species, differing from occidentalis as
tollows :—
T. isocomeé 3.
Smaller, about 9 millim. long ;
abdomen less tapering.
Markings pale cinereous.
Labrum with a little apical pit
full of white pubescence, its sides
projecting and subdentiform.
Labrum all black.
Stripes on mesothorax hardly
separated, 7. ¢, the area between
them pubescent.
Scutellum strongly bilobed.
Lower part of pleura covered
with hair.
Wings shorter, hyaline; venation
more ferruginous, marginal cell
more obtuse,
Hair on inner side of basal joint
of hind tarsi black.
Second abdominal segment with
large pyriform lateral hair-patches,
pointed antero-mesad.
T. occidentalis 3 (from Colorado).
Larger, about 11 millim. long;
abdomen more tapering.
Markings cream-colour.
Labrum with two minute apical
projections, but no pit.
Labrum with a red spot on each
side.
Stripes on mesothorax well se-
parated.
Scutellum feebly bilobed.
Lower part of pleura nude,except
on anterior margin.
Wings longer, brownish; vena-
tion more fuscous, marginal cell
more acute.
Hair on inner side of basal joint
of hind tarsi orange-ferruginous.
Second abdominal segment with
rather small lateral patches anterior
to the band.
The mandibles of J’. csocome are perfectly simple, red in
the middle ; the antenne are black, the flagellar joints with
obscure reddish spots; the hind coxe are mainly red; all the
trochanters, femora, tibie, and tarsi are red; the scutellar
teeth are short and black; the hind tibial spurs are black.
Eyes (at least when dry) light green.
T. segregatus (Epeolus occidentalis, var. segregatus) appears
some Parasitic Bees. 39
to be also a distinct species, allied by the punctuation of the
pleura to 7. pectoralis (Rob.).
Triepeolus helianthi (Rob.).
T have confused this with 7. Cressont, which it very closely
resembles. I have a female from Lllinois, sent by Robertson
years ago as Hpeolus mercatus. Another female was collected
by Mr. C. E. Mead, Sept. 19, 1898, at the Experiment
Station near Aztec, New Mexico, at flowers of Verbesina en-
celioides. A specimen from near San Ignacio, N. M., formerly
recorded as Cresson, is nearly 18 millim. long, but appears to
be the same species.
Triepeolus helianthi, var. arizonensis, var. nov.
3 -—Small, length about 8 millim.
Wings clearer, marginal cell considerably shorter and more
rounded at end; labrum red; pubescent margin of first abdo-
minal segment not broken anteriorly or posteriorly ; fringe
on fourth and fifth ventral segments fuscous.
flab. Phoenix, Arizona, at flowers of Helianthus annuus,
October 9 (Cockerell).
Perhaps a distinct species. The legs are coloured as in
helianthi, the anterior legs being very dark.
Triepeolus Cressoni (Rob.),.var. fraser, var. nov.
3 .—Variable in size, from about 8 to nearly 11 millim.
Antenne and labrum entirely black ; mandibles black with
a red spot ; hind femora red, middle femora with a black mark
above; tegule reddish to piceous; nervures black except
towards base of wing, where they become reddish ; hair-stripes
on mesothorax broad, flame-like, connected with a broad
hairy anterior border.
Known from helianthi by the entirely hairy pleura, and
from occidentalis by the black anterior femora &ce.
Hab. Beulah, New Mexico, about 8000 ft., June 29, at
flowers of Frasera (W. P. Cockerell), July 12 (W. P. Ckil.),
July 12 (7. D. A. Chil.) ; Las Vegas, N. M., at flowers of
Spheralcea Fendleri lobata, July 24 (W. Porter). I think the
insect recorded from Beulah by Mr. Viereck as Z. occidentalis
must have belonged to the present form.
Epeolus crucis, sp. n.
? .—Length about 74 millim.
This is the species, found at Las Cruces by Professor C. H. T.
4() Mr. T. D. A. Cockerell on
Townsend, which has passed as Z. compactus, Cresson, in New
Mexico, having been so identified by Mr. Fox. It may have
been included by Cresson among his specimens of compactus;
but it surely is not the species described under that name.
From the description (Tr. Am. Ent. Soc. vii. p. 89) it differs
thus :—Not especially compact, the abdomen at least twice as
long as broad; pleura with the upper part densely white-
hairy, the lower densely and coarsely rugoso-punctate, nearly
free from pubescence ; pale (hair) markings white, not buff;
abdomen strongly pruinose all over with fine pubescence, so
that the usual black markings, while indicated, are more or
less obscured, the black surface being nowhere exposed ; the
apical white bands on the first four segments are broad and
entire, and are somewhat emphasized by the fact that the
apical margins of the segments, beneath the pubescence, are
white ; the transverse dark band (grey because pubescent)
on the first segment is much produced and quite attenuated
laterally. Labrum, mandibles, and first three joints of an-
tenn ferruginous, the flagellum brownish grey with a sort of
silvery sheen above, ferruginous beneath ; anterior middle of
mesothorax with a white hair-patch, no separate stripes ;
scutellum faintly bilobed, black with two reddish spots, lateral
teeth red, quite sharply pointed, not extending so far as
scutellum ; tegule bright orange-ferruginous, Wings rather
short, faintly dusky, with an apical cloud ; stigma and nervures
of basal half of wing ferruginous, nervures of apical half dark
fuscous ; marginal cell rounded at end, appendiculate. Legs
ferruginous, the femora strongly infuscated, spurs light ferru-
ginous; silvery area on last dorsal segment of abdomen
inconspicuous.
Epeolus beulahensis, sp. n.
¢ .—Length 7 millim.
Black with yellowish-white markings due to pubescence ;
face, including clypeus, covered with silvery-white appressed
hair ; mandibles and labrum dark ferruginous ; eyes strongly
converging below; eyes (dry) grey ; antenne long, brown-
black; end of scape and the two following joints ferrugi-
nous beneath; tubercles and tegule ferruginous ; scutellum
entirely black, faintly bilobed, the lateral teeth very short ;
thorax, including pleura, covered with pubescence, except
disk and anterior margin (except two broad short stripes) of
mesothorax, anterior half of scutellum, metathoracic enclosure,
and a spot on each side of metathorax, which are bare and
consequently black ; legs clear red, including the spurs; an-
terior femora except knees, and anterior tibiz except ends,
some Parasitic Bees. 41
black ; middle femora with a black stripe above. Wings quite
clear, except the broad apical margin, which is faintly dusky ;
nervures and stigma piceous; marginal cell obliquely sub-
truncate, minutely appendiculate; second submarginal cell
nearly as broad above as third. Abdomen thick-fusiform, the
black areas very distinct, that on first segment a broad trans-
verse band, obliquely truncate laterally ; hair-bands on first
and second segments narrowly interrupted medially ; second
with large lateral oval spots touching the band ; light areas
on fifth segment just meeting on disk ; pygidial plate ferru-
ginous, broadly triangular, but subtruncate at tip; second
ventral segment white with a large black (nude) patch on each
side ; third and fourth with white hair-bands.
Hab. Beulah, New Mexico, prox. 8000 ft., July 11
(Cockerell) .
Allied to £, autumnalis, Rob., but differs by the clear wings,
small spines of scutellum, &c.
Epeolus olympiellus, sp. n.
6 .—Length about 74 millim.
Stout, with an oval abdomen, black with the usual yellowish-
white markings; labrum entirely black, with two prominent
apical projections ; middle part of mandibles bright ferrugi-
nous ; lower part of face, down to middle of clypeus, covered
with silvery hair; clypeus densely rugoso-punctate ; scape
black ; tubercles ferruginous; tegule dark ferruginous, mi-
nutely and densely punctulate. Wings nearly clear, apical
margin broadly dusky, nervures and stigma piceons; marginal
cell obliquely subtruncate, minutely appendiculate; second
transverso-cubital nervure with its upper half wanting; if it
were complete, the second submarginal cell would be fully
twice as broad above as the third. Femora black, the knees
red; tibie with the greater part black; tarsi ferruginous ;
spurs light ferruginous ; lower part of pleura thinly pubescent,
densely rugoso-punctate; mesothorax with the usual two
stripes widely separated, and without erect pubescence ; scu-
tellum subbilobate, wholly black, the lateral teeth short, but
very distinct. Abdomen with the black areas well-defined ;
apical bands on segments 1 to 4 interrupted in the middle, the
approximating portions of the bands on 2 to 4 club-shaped ;
black area on first segment a very broad band, obliquely
truncate laterally, and not produced much more than halfway
to the lateral margins; band on second segment broadened at
the sides, but no oval patch ; apical plate broadly rounded,
black ; ventral surface with two broad white hair-bands,
42 Mr. G. A. Boulenger on a
Hab. Olympia, Washington State, July 2, 1896 (Trevor
Kincaid).
Allied to E. interruptus, Rob., but basal joints of antennz
not red, legs with much more black, postscutellum without a
tooth, &e.
Phileremus americanus, Cresson.
Hab. Beulah, N. M., at flowers of Apocynum androsemt-
folium, July 8 (W. P. Cockerell).
New to New Mexico. Cresson’s description is not suffi-
ciently detailed, but I think my identification is certainly
correct. This species and P. mesille, Ckll., are to all intents
and purposes Hpeolus with two submarginal cells. I am
convinced that these insects stand nearer to Hpeolus as restricted
by Robertson than that genus does to T'riepeolus.
The black band on the first abdominal segment is much
less produced laterally in P. americanus than in P. mesille.
The fringes of erect hairs on the fourth and fifth ventral seg-
ments of P. mesille are white. While P. americanus flies in
summer in the Canadian zone, P. mesil/e is a spring insect
of the Middle Sonoran; a male before me was collected at
Mesilla Park, N. M., May 7, at flowers of Dthyrea Wislizentt.
It has the face densely covered with white hair.
The female of P. mesil/e has not been described ; but I
have a specimen (CkIl. 2810) collected at flowers of Sophia
at Mesilla Park. The abdomen is longer than in the
male, and the hind margins of the first four segments
are broadly orange, with a coppery lustre, and practically
hairless, though perhaps denuded. More than the apical
half of the fifth segment is orange, and the very distinct
white lunule is bordered behind by brown. The pygidial
plate is truncate. The knees, tibize, and tarsi are all ferru-
ginous. The flagellum is ferruginous, darker above. The
disk of the mesothorax is dark brown, and the two light stripes
are very distinct; in the male there are two very large light
patches on the anterior part of the mesothorax.
11].—Description of a new Genus of Frogs of the Family
Dyscophide, and List of the Genera and Species of that
Family. By G. A. BOULENGER, F.R.S.
[Plate IL]
COLPOGLOSSUS.
Pupil vertically elliptic. Tongue large, oval, entire and
free behind, forming a plicate pouch at the point of its poste-
new Genus of Frogs. 43
rior attachment. Palatine teeth forming a long transverse
series narrowly interrupted in the middle. ‘T'wo denticulate
transverse dermal folds in front of the pharynx. Tympanum
hidden. Fingers free, toes webbed at the base, the tips not
dilated; outer metatarsal bound together. Coracoids strong ;
precoracoids very weak, ligamentous; no omosternum ;
sternum a large cartilaginous plate. Diapophyses of sacral
vertebra moderately dilated.
Colpoglossus Brooksti. (Pl. II.)
Habit very stout ; head strongly depressed, once and two
thirds as broad as long; eye small, interorbital width three
times the width of the upper eyelid. Fingers short, obtusely
pointed, first shorter than second; subarticular tubercles
indistinct ; a large, oval, inner metacarpal tubercle. ‘Toes
short, blunt, with a very short basal web; subarticular
tubercles feebly prominent; a rather large and very promi-
nent inner metatarsal tubercle. ‘The tarso-metatarsal articu-
lation reaches the eye. Skin of head and body granulate, of
belly and limbs smooth. Yellowish above, elegantly marked
with dark brown lines, which form a network on the sides
and limbs; a )-( shaped dark brown, light-edged marking
on the head and nape, each of the longitudinal branches
bifurcating in front and behind; two chains of small black
spots, some with light centre, along the middle of the back ;
lower parts white, throat with wrinkle-like transverse brown
lines.
From snout to vent 50 mm.
A single specimen from Bidi, Sarawak, discovered by
Mr. Cecil J. Brooks in a hole whilst prospecting, and pre-
sented by him to the British Museum.
The discovery of a member of the family Dyscophide in
Borneo is a very important addition to our knowledge, all
the members of this natural group being inhabitants of Mada-
gascar, with the exception of the Burmese Calluella guttulata.
So many genera and species have been added to this family
since the publication of the British Museum Catalogue (1882)
that a complete list, such as is here appended, will be welcome
to herpetologists and to students of geographical distribution.
I, Pupil vertical ; palatine teeth in long transverse series.
A. Preecoracoids ossified ; tips of fingers and toes not dilated.
a, Sternum large.
1. Dyscophus, Grand. 1872.—-Madagascar,
1. insularis, Grand. 1872,
2. Guinett, Grand. 1875.
3. Antongilit, Grand. 1877,
At On a new Genus of Frogs.
4. Grandidiert, Blgy. 1896.
5. Alluaudi, Mocq. 1901.
b. Sternum small.
2. Calluella, Stol. 1872.—Burma.
1. guttulata, Blyth, 1855.
B. Precoracoids not ossified.
a. Sternum large ; tongue forming a pocket behind; tips of fingers
and toes not dilated.
8. Colpoglossus, Blgr. 1904.—Borneo,
1. Brooksu, Blgr, 1904.
6. Sternum small; tips of fingers and toes dilated.
4, Piethodontohyla, Blgr. 1882.—Madagascar.
1. notosticta, Gthr. 1877.
2. inguinalis, Bley. 1882.
3. brevipes, Blgr. 1882.
II. Pupil horizontal.
A. Palatine teeth in long transverse series.
a. Preecoracoids ossitied ; tips of fingers and toes dilated.
a. Fingers and toes free.
5. Mantipus, Peters, 1885,—Madagascar.
1. Hiuldebrandti, Peters, 1883.
8. Fingers and toes webbed at the base.
6. Platyhyla, Blgr. 1889.—Madagascar.
1. grandis, Blgr. 1889.
2. verrucosa, Mocq. 1901.
b. Preecoracoids not ossified ; tips of fingers and toes not dilated.
7. Phrynocara, Peters, 1885.—Madagascar.
1. tuberatum, Peters, 1883.
B. Palatine teeth in one or two small groups or absent ; precoracoids
ossified; tips of fingers and toes dilated.
a. Two small groups of palatine teeth.
8. Platypelis, Blgr. 1882.—Madagascar.
1. Cowaniti, Blgr. 1882.
2. pollicaris, Blgr. 1888.
b. A single small group of teeth in the middle of the palate.
9. Cophyla, Bttgr. 1880.—Madagascar.
1. phyllodactyla, Bttgr. 1880,
c. No teeth on the palate.
10, Anodontohyla, F. Mull. 1892.—Madagascar.
1. Boulengert, F. Mull. 1892.
EXPLANATION OF PLATE II.
Colpoglossus Brooksii, upper view, natural size. a, open mouth (x 2);
6, lower view of hand (xX 2); e, sternal apparatus (x 13),
The Collections of William John Burchell. 45
IV.—The Oollections of William John Burchell, D.C.L., in
the Hope Department, Oaford University Museum.
I. Introduction. By Epwarp B. Poutton, D.Sc., M.A.,
Hon. LL.D. (Princeton), F.R.S., F.L.S., F.Z.S., F.G.S.,
President of the Entomological Society of London, Hope
Professor of Zoology in the University of Oxford, Fellow
of Jesus College, Oxford.
[Plate III.]
Wukry, in June 1893, I was first placed in charge of the
Hope Collections of the University of Oxford my attention
was at once arrested by specimens of insects and other arthro-
pods collected in South Africa about ninety years ago, and
much larger numbers from Brazil with dates going back
about three-quarters of a century. I was struck by the
precision and detail of the data and by the existence of
numbers which evidently referred to a diary. Three manu-
script note-books were eventually found in the Hope Library,
and these showed that the material had been collected by the
great naturalist William John Burchell, truly described by
Swainson as “one of the most learned and accomplished
travellers of any age or country—whether we regard the
extent of his acquirements in every branch of physical science
or the range of the countries he has explored” (‘ Cabinet
Cyclopedia’ of Dionysius Lardner, vol. Taxidermy &c.,
Appendix, p. 383: London, 1840).
The first necessity was to ascertain if the data were as
accurate as they were full and elaborate. A single quotation
from the Brazilian note-book throws much light upon this
important question. From Oct. 6th to Nov. 16th, 1825,
Burchell was upon an expedition into Minas Geraes from
Rio de Janeiro. ‘The following note refers to the beetles
collected on four days towards the end of this journey :—
“‘ All the Coleoptera of ard, 4th, 5th, and 6th have since
been marked 4. 11. 25, as the different day’s collections being
mixed in one paper could not be distinguished. They were,
however, all caught in forests or on the edge of forests,
Some other Coleoptera caught on these same days, but which
were put up in separate papers and marked, are properly
distinguished by their labels, but those certainly of the 4th
are marked 4. 11. 25, with the 4 underlined, and consist of
only a few minute insects caught at night by the candle,”
1t is obvious that the man who wrote that note was a man
46 Prof. E. B. Poulton— The Collections
to be trusted, and the immense numbers of his unpublished
observations on natural history at once acquire the value of
records by a trained naturalist with a fanatical love of truth
for its own sake. Here, then, was the means of carrying
back the detailed record of the occurrence of many thousands
of species in two most interesting parts of the world, and to
construct a trustworthy standard by which to measure the
rate of future change; for one great justification of the
immense funds which are expended on museums is that they
will serve this very purpose for generations yet to come.
The critical examination of the Burchell specimens proves
that with ordinary care and the exclusion of light insects’
pigments will endure for probably an indefinite period.
Many of these specimens have not had ordinary care during
a part of their history, the African collection being especially
attacked by Anthrenz, probably between 1825 and 1830, when
Burchell was travelling in Brazil. But even upon the most
fragmentary of these the patterns are still quite distinct and
have undergone hardly any change.
The collection, combined with the manuscript notes on
labels and in the note-books, furthermore supplies a great body
of observations on habits, instincts, &c. which are still im-
perfectly known, and often altogether unknown. In many
cases | find the records of interesting observations since made
and published by others, such as the sound produced by the
South-American butterfly, Ageronia feronia, described by
Darwin in the “ Voyage of the ‘ Beagle’”’ (London, 1876,
pp. 33, 84), or the habits of the driver-ant (/ccton) and leaf-
cutting ant (@codoma), described by Darwin, Belt, Bates, Ke.
When I first began to arrange for the publication of an
account of the Burchell Collections at Oxford it was intended
to prepare an introductory memoir upon the life of the great
naturalist himself; but this proved to be too extensive an
undertaking for these pages, and it is hoped that the “ Life”
will appear as a separate work at no distant date. In the
meantime a brief abstract of the chief facts which I have been
able to bring together is set forth below as an introduction to
the papers which will follow.
William John Burchell, the eldest son of a nurseryman at
Fulham, was born about the year 1782. He received an
excellent education, as is proved by the admirable style of
his published works, the facility with which he wrote Latin,
and the number of sciences with which he was intimately
acquainted. His manuscript notes on South-African insects
in the Hope Department are written on the blank sides of
the pages of his French exercise-book—a history of Greece
of William John Burchell. 47
translated into French in 1794, when he was about twelve
years old. Burchell was also an accomplished artist and
musician. He must have had a remarkable constitution, for
he enjoyed uninterrupted good health and vigour throughout
his long and, with the exception of native attendants, solitary
journeys. He laboured throughout the whole of the time
with astonishing energy—collecting, observing, recording,
sketching, and writing detailed journals. The details of his
tragic end in his eightieth year also show that he possessed
extraordinary resolution at that advanced age.
Burchell’s features at about thirty-four years of age are
preserved in a drawing made by J. 8. Cotman in 1816, the
year after the South-African travels had come to an end.
The drawing was etched by Mrs. Dawson Turner, the grand-
mother of Sir Joseph Hooker. The portrait, of which there
is a copy at Oxford, brings back to us Burchell in the full
vigour of manhood. ‘The face is highly intellectual and
indicative of strong purpose and resolution, yet singularly
attractive, even winning. The appreciation and description
in his South-African travels of many a quaint incongruity
shows that he possessed an ample fund of humour. His
invariable breadth of view and justice are well seen in the
calm discussion of the methods and results of missionary
labours and his accounts of the shabby treatment he received
from some of the Boers, in which he always warns the
reader against coming to a too hasty conclusion as to the
character of a whole people.
In 1805, when he was about twenty-three, Burchell was
appointed “ Schoolmaster and acting Botanist”’ at St. Helena
by the East India Company, and he remained in the island for
five years, until his departure for Cape Town in order to begin
his South-African travels. He was elected a Fellow of the
Linnean Society, Feb. 15, 1808. The romance of his life
happened in St. Helena, and probably exerted a profound
influence upon his character, explaining much that is difficult
to understand, and especially the secretive barren period which
followed his return from Brazil in 1830. His father had
disapproved of Burchell’s engagement to a lady in Fulham,
and had, perhaps, obtained the appointment in St. Helena,
hoping that everything might be forgotten. But the two
still corresponded, and Burchell persuaded the lady to come
out and join him in the island. During the voyage someone
on the ship—it is said, the captain—fell in love with her and
married her. Burchell had always been a naturalist and
collector, but it is probable that the terrible shock drove him
into these pursuits and away from companionship with his
48 Prof. E. B. Poulton—The Collections
fellow-men, for consolation or, at any rate, oblivion. Natural
history pursued in this spirit, especially when habits become
fixed and deepened with advancing age, is only too likely to
lead to the non-productive life of the recluse, poring for long
years over his collections, jealously guarding them from the
sight of others, and yet giving no account of them to the
world.
We now enter on the next great period of his life, the five
years (1810-1815) of splendid work in South Africa. ‘The
first part of his travels, discoveries, and observations are
described in the classical ‘ Southern Africa’ (vol. i. London,
1822, vol. ii. 1824), covering the period between his landing
at Cape Town on Nov. 26, 1810, and his departure from
Litakun on Aug. 3, 1812. The work contains a large and
excellent map, showing the whole of his route. He had
intended to follow up these volumes by a complete account
of the whole journey, but this was never accomplished, and
the manuscript of his journal and other materials from which
it might be written have not yet been found. The fine
collection of insects which he made in St. Helena and South
Africa was almost destroyed by neglect, probably during his
absence in Brazil (1825-30), but hundreds of species can be
named from the fragments preserved in the Oxford Museum.
The botanical collections, now at Kew, did not suffer in the
same way, and are in excellent condition.
Burchell remained in England during the ten years which
intervened between his South-African and Brazilian journeys.
He sowed in his garden at Fulham hundreds of South-
African seeds and some from St. Helena, keeping a careful
record, now preserved at Kew, of the dates at which they
came up. On Sept. 30th, 1817, he presented forty-three
skins of South-African quadrupeds to the British Museum,
and the neglect of these specimens, many of them unique,
was the cause of his quarrel with that Institution (‘ Southern
Africa,’ vol. i. p. 383 &c., vol. i. p. 336 &c.).
A letter to Sir William Hooker, dated March 31, 1819,
shows the care he took to suggest appropriate names for the
new species which he had discovered :— I should mention
that it was my practice when on my travels to give such
specific names to my plants as the view of them in their native
place of growth naturally suggested, without attending to
their being new or not, which | had not always on the spot
time to ascertain; but my object in thus naming them was
that on my return to England I should find all the new
species with more appropriate names than an inspection of
the dried specimens im the herbarium might probably suggest
of William John Burchell. 49
to me.” An examination of his Brazilian note-book proves
that he adopted the same excellent method in his later travels.
In 1819 Burchell was called to give evidence before a
Committee of the House of Commons on the question of
emigration as a relief from pauperism. In his evidence,
which occupied nearly three hours, he advocated the suit-
ability of the Albany district in the easternmost part of Cape
Colony. In a few days the Committee reported, and a grant
of £50,000 was voted for this purpose. Burchell then ampli-
fied and published his evidence in a pamphlet, ‘ Hints on
Emigration to the Cape of Good Hope’ (London, Aug. 1819).
This was savagely attacked in the ‘ Quarterly Review ’ for the
following November, and Burchell replied in a sheet of four
pages bound into the first volume of his ‘Southern Africa.’
Looking at the controversy from the standpoint of the present
day, there can be no doubt that Burchell was entirely right
and that the loyalty of the Grahamstown district, which has
shone so conspicuously during recent years, is in large part
the outcome of his wise advice.
More than all the work described above, the arrangement
of his South-African collections and the preparation of the
two volumes on South Africa occupied Burchell’s time until
he began to get ready for his next great journey.
Of the five years in Brazil very little is known, mainly
because Burchell published nothing after his return. Hooker’s
‘ Botanical Miscellany’ (vol. 11. 1831, pp. 128-133) contains
some very interesting extracts from his letters to Sir William
Hooker, and the life of Burchell in the ‘ Dictionary of
National Biography’ (vol. vii. London, 1886, p. 290) also
has an excellent short account of these travels.
Inasmuch as the Brazilian collections of insects &c. are far
more extensive than the African, and are, considering their
age and the vicissitudes through which they have passed, in
excellent condition, the following papers will be chiefly con-
cerned with them, and it becomes of the utmost importance to
show the exact route traversed by Burchell. ‘This is clearly
shown by the map on the accompanying Plate III., prepared
from the data obtained by Miss Cora B. Sanders, of Lady
Margaret Hall, Oxford. The data were gained by a careful
study of Burchell’s manuscript note-books at Oxford, and
especially the Index to the Localities of the Plants and
Insects. Miss Sanders was able to find many of the names
which have disappeared from modern atlases by an exami-
nation of the older maps of Brazil in the possession of the
Royal Geographical Society. ‘The numerous smaller villages,
halting-places, streams, &c. mentioned in the manuscript
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 4
50 Prof. E. B. Poulton—The Collections .
note-books or upon the specimens themselves will always be
described as between or near places which have been thus
identified and are indicated upon the map. As regards Bur-
chell’s two expeditions from Rio de Janeiro into Minas Geraés
and the Organ Mountains, hardly any of the places mentioned
could be found; but it is clear from the time occupied and
the account of the work done that he did not travel far.
Following the exact data which Burchell always records,
we find that he left Fulham at 9.30 A.M. on March 10, 1825,
and sailed from Portsmouth at 9 A.M. on March 15th. The
main outlines of the journey are set forth below in a tabular
form copied from a paper gummed into one of his manuscript
note-books in the Hope Department, viz. ‘ Index to the Lo-
calities of the Plants in the Brazilian Herbarium &c., serving
also for the Localities for the Collection of Insects &e.” ‘The
only modification of Burchell’s original table is the insertion
of the two expeditions from Rio in their proper positions in
time, instead of placing them at the end, and thus putting the
three separated periods in Rio itself in juxtaposition.
| | TIME.
PLACE | Dates. [SS Se
| | Monrus. Days.
OVSDGE titi vamskepeeeilOl lh ol eek bee- lara pie
A (Op ano tS Ul pe Fy
Tn Portugal 14 jects f- | 195, 5. 25 | 2 0
a ee
WO ABO iach Plait Se phe ae ere 5
Madeina pis nideeora te 29, 5. 25 1
WiGYVASCI2 eatin aera | east ee | Sean 2
Meneritle on. sete cake aks 1. 6. 25 | sxene 2
NOVAS ese cr cteer fete | a 1 16
ay yf atx
Rio de Janeiro........ | 1 a 10. bE
a yhoae | | 6. 10. 25]
| Minas Geraes ........ | 116. 11. 256 i 4*
| > =
(eee sf WG ries
| AiO de JaneITO sini tes | ) 5. 2. 56
| Or Me Gee | Geo e
| Organ Mountains...... | 2 3. 26( De
=e ee {eo toO {total tim
Rio de Janeiro........ | ) 10. 9. 564 asea Rio] a 16
* This number is given by Burchell. He probably deducted the days
spent in travelling from and to Rio.
of William John Burchell. aE
TIME.
PLACE. DarTEs.
Monrus. Days.
\USTC SRS hd 7 ee | oe 3
OCU kena sia cyeceis as ee i 36 2 21
REGARD IA: ais ls. 117 a 7 1 14945)
i eravelling,... (625. - 4262, by js omnes aids 3
2 Ov fa wTly ed
BR Battilioy 9, oh tac Sad 1a. x on G 4
Sie rns Hy, fihine im! fae Dae |
Mita eMME ys 35.5 enn 3: ce iW a 3 8
. 07 Weta a Sle wh
7) eee ering os 9 18
ey ates 28 1 ot | “a
Weavellmes si. ou. Je 6. 3 rd fe 2 22
i a ax ; pe ror “ea LS a LL
Portocmeal oi. ek sc Hs He 954 5 18
Travelling (Tucantins) . 110 “i a0 1 13
ez a Rw > ae 10. 6. 29 sod Wy dite
PAA Meike Sor ajohasehr hn 2)» 110. 2, 30} 8 0)
RECON ets net are te shall) m oe lvepdiite te 1 15
Burchell landed at Dover on March 24th, 1830, and
reached his home in Fulham on the following day.
The journey originally planned by Burchell was far more
extensive. Thus he wrote to Sir William Hooker from Rio
(July 8th, 1826) :—
“. .. Itis at least my wish to visit the city of S. Paulo,
and thence by land through the provinces of Goyaz, Cuyaba,
and Matto Grosso into Peru, having the city of Luzco as my
principal object; and after doing in Peru as much as m
time (for my family prefer my being in England) and slender
means will allow me to do, I should wish to proceed by land
to Arequipa, Potosi, Salta, &c., &c., to Buenos Ayres, and
thence to my home at Fulham. . .”
A letter nearly two years later to the same friend explains
the change. It is dated from Goyaz, April 25, 1828 :—
At
52 Prof. E. B. Poulton—The Collections
“|, Thave kept my original plan always in view, and
had advanced thus far on my way to Peru &c. when letters
from Fulham overtook me, stating that my dear father’s
health, from the infirmities natural to his age, was gradually
declining, and that it was his wish and that of the rest of the
family that I should return directly to England. Whatever
regret I may feel at thus relinquishing my American travels,
and whatever disappointment I may experience from a prema-
ture return, I have no hesitation whatever in preferring filial
duty to science and the gratification of my own inclinations.
I have therefore greatly altered my plans, and instead of
ending this journey at Beunos Ayres, shall, Deo volente, end
it at Pard, where I shall embark for England.”
Burchell was not destined to see his father again, for
Matthew Burchell died soon after this letter was written, on
July 12, 1828.
An excellent brief account of the Brazilian journey is given
in a letter to Sir William Hooker, written from Burchell’s
home at Churchfield House, Fulham. Much of it is printed
in ‘ Hooker’s Botanical Miscellany’ (vol. i. 1831, pp. 128-
133). The original letter, together with the others which
have been made use of on the present occasion, are preserved
in the Herbarium of the Royal Gardens at Kew. ‘The letter
is dated Nov. 1, 1830 :—
“T Jeft England in March 1825, passed two months at
Lisbon and in the vicinity: landed at Rio de Janeiroin July,
where I continued making collections in botany, entomology,
and geology, &c., till Sept. 1826, during which period I
visited a part of Minas Geraés. While at Rio I made some
drawings of landscape, among which was a panorama taken
from a hill in the middle of the city ; many astronomical,
philosophical, and geodetical observations. I finally quitted
Rio in Sept. 1826, and proceeded by sea to Santos, where I
remained three months, and then proceeded and took up my
station in a solitary hut in the midst of forests at the foot of
the great range of mountains, for the purpose of exploring
them at leisure. My next station or headquarters was at the
city of S. Paulo, nearly under the tropic of Capricorn, where
I remained about seven months, extending my excursions in
various directions. Having there purchased a troop of mules
and engaged the requisite muleteers, I travelled northward,
and finally took up my station at the city of Goyaz, being
the first and only Englishman who has entered that province.
There I passed the rainy season of 1827 and made large
collections, being detained there nine months, owing chiefly
to the difficulty of finding the means of conveyance for my
of William John Burchell. 53
baggage. At length, resuming the road and still continuing
Northward, I reached in November 1828 Porto-Real, on the
great river Tucantins. Here I remained till the proper
season for embarking, and, descending the stream, at all times
rendered dangerous by numerous rocky falls, rapids, and
whirlpools, I made considerable collections on ground over
which no scientifie traveller had ever passed. I ‘completed a
survey of the whole length of this voyage, fixed by numerous
astronomical observations. Finally, I arrived at the city of
Para in June 1829, and, while waiting till February for a
convenient opportunity ‘of embarking for England, added
largely to my collections both in zoology and botany. Of
this city I made a panorama, which, with that of Rio, [ hope
perhaps to succeed in getting engraved, together with my
landscapes &c. Of insects I found from 16 to 20 thousand
specimens (at a guess). Of birds I shot and preserved 362
species. In the other classes a proportionally smaller
number. I am not aware of any part of my collections being
lost, though I daily lament my inability to unpack them for
want of room in the house. ‘The space I require is large, and
I have some hesitation in building on bishop’s land, unless it
were possible to enfranchise it. I fear I shall lose much
time before I am comfortably settled: nothing is more dis-
tressing to me than thus to be forced to delay my labours in
arranging my collections and rendering them useful to science.
You, who are so great an example of ‘industry, complain also
of overwhelming collections, and feel the necessity of manual
help. But I have nowhere beheld an herbarium so large as
my own; and, added to this, I cannot bring my mind to
abandon any branch of natural history for the sake of giving
more time and attention to any one in particular ; although [
know this is wrong and can never lead to perfection in any.
Still the contemplation of the whole system of created
objects is so fascinating that it is very diffic{ult to] turn
away from all but a few.”
These latter sentences, together with the considerations
mentioned on pages 47, 48, help us to understand Barchell’s
unproductive later years. Living secluded in the midst of
his vast collections, he wandered from one point to another
without the stimulus to work out any one part thoroughly
which contact with his brother naturalists would have supplied.
Furthermore, he belonged to that class of men, much rarer now
than formerly, who value and gloat over collections as collec-
tions. His letters, even to his most intimate friends, such as
Sir William Hooker, as well as many records preserved in his
note-books, show that he jealously watched over the material
~
D4 Prof. EK. B. Poulton—The Collections
of his collections, and indicate that he suffered much anxiety
on this account. His will, which was proved for probate at
under £4000, also shows that he was right in the contention
that he could not afford to employ assistance in the skilled
mechanical work which was required, while his almost too-
scrupulous care and attention to detail must have consumed
an immense amount of his time. Sir William Hooker had
evidently urged him to employ a curator or librarian, for
Burchell’s letter of June 25th, 1835, contains the following
passage :—“ After the consumption of so much of my property
by my travels and the disinterested pursuit of science all the
rest of my life, the obtaining of assistance by payment is
quite out of the question.” Similar advice had been given
and answered in the same sense five years before.
The degree of D.C.L. Honoris Causa was conferred upon
Burchell by the University of Oxford on May 8th, 1834.
Daubeny, the Professor of Botany, had given his inaugural
address on May Ist, and the first lecture of his first course
(on Vegetable Physiology) was delivered on May 8th. It
seems probable that Burchell came to Oxford in order to be
present, and that the occasion was selected for the conferment
of the degree.
There is no doubt that Burchell expected a government
pension and that he bitterly resented what he regarded as un-
deserved neglect. Hence, to the other causes which operated
to prevent productive work, we must add the brooding
melancholy and the bitterness of a disappointed man, the
man with a grievance.
It is probable that he freely communicated his ideas on
this subject to his friend Swainson, and that the attack on
the government for neglect of Burchell was a result of their
intimacy. ‘These severe criticisms may be seen in Swainson’s
article quoted on page 45. The same article is probably
responsible for exaggerated statements, which have been con-
stantly repeated, as to the condition of his collections and the
assertion that they were never unpacked. It was probably
an extreme way of indicating the injury which science was
receiving because. Burchell remained unassisted. But it was
certainly exaggerated. In the note-books at Oxford there is
the record of the different dates at which he accomplished
the setting of the various groups of Brazilian insects. More-
over, the beautifully written labels which nearly all specimens
possess are very different from the hasty but distinctly
legible notes made in the field. Many specimens still retain
both labels, but generally the older ones have been discarded,
To this grievance was added the further sense of failure in
of William John Burchell, 59
that others were continually gaining credit for work which
he had done but had not published, Thus he wrote to Sir
William Hooker on Sept. 3, 1832 :—
‘T am vexed almost to death at all my fine collections
being thus shut up from me while I am daily losing portions
of the only reward a traveller has—that of his discoveries.
... [trust that [in] future my work will make more
show, at least to the world.”
A few years later the same kind friend seems to have made
a great and probably a final effort to induce Burchell to
publish his results. Burchell’s reply is dated June 25th,
1835 :—
‘ Wyom the manner in which you express yourself with
regard to my botanical collections you appear to be under
very erroneous impressions, for to say that I ‘ wild not publish’
is quite the opposite to what has ever been my intention, and
the almost only pleasure I had in my travels to alleviate the
excessive toil of forming them was the anticipating of the
gratification of publishing them at my return to Europe, and
of obtaining the satisfaction of being useful to science, and of
securing the honor [spelt thus, according to his custom] due
to my discoveries; and if I have been, and still am being,
robbed of those honors by others, who, having less on their
hands than I have, can run the publishing race with more
expedition, I feel most sensibly the injury I sustain. Many
circumstances have unfortunately concurred hitherto to tie up
my hands, but I do and shall ever look to Natural History as
a most delightful and congenial employment for my future
years.”
Probably owing to the combination of causes set forth
above and their deepening effect as years went on, Burchell
became more and more of a recluse, and kept his collections
more and more from the sight of other naturalists. The
climax was reached when he refused the request of his old
friend to allow his son, Sir Joseph Hooker, to see the collec-
tion of St. Helena plants, in order to help in the production
of a work upon the flora of that island.
Towards the end of his life Burchell must have come to
realize that his methods could lead to nothing. He committed
suicide on March 23rd, 1863, in his eightieth year. It is
stated by C. J. Féret, in ‘ Fulham Old and New’ (London,
1900), that he “shot himself under the large cedar tree in
front of Churchfield House. The wound not proving fatal,
he terminated his existence by hanging himself in a small
out-house at the back.”
Burchell’s collections were not specially mentioned in his
56 Mr. R. I. Pocock on a new
will (dated March 2, 1841). Upon his death in 1863 they
came into the possession of his sister, Miss Anna Burchell,
who offered the whole of them to the University of Oxford
in the following year upon the condition ‘ that separate rooms
shall be set apart for them, and that the whole be put out,
set up, and systematically arranged, and be called ‘The
Burchell Collection’ or presented to the Museum by Wm. J.
Burchell, Esq., D.C.L.” The Delegates of the Museum were
unable to accept these conditions. A few months later
Miss Burchell wrote (April 8, 1865) concerning “ the collec-
tions in Zoology and Entomology,” “1 am still desirous, in
accordance with what I believe to have been his [Dr. Bur-
chell’s] wish, of presenting the same to the University of
Oxford.” The only condition was “that the Collections
should be distinguished as those of my late Brother.” This
offer was gratefully accepted, and in a few weeks the collec-
tions arrived. About the same time the immense Herbarium
was offered by Miss Burchell to the Linnean Society, which
was unable to accept it. A little later it was presented to
the National Collection at Kew.
In drawing up this brief account of Burchell, as a preface
to the description of his collections, I desire above all to
acknowledge the kind help I have received from Miss Cora
B. Sanders in the study of Burchell’s manuscript at Kew and
Oxford, and of his collections in the Hope Department. It has
been already mentioned that the map forming Plate ITT. is en-
tirely due to Miss Sanders’sresearches. I havealsoreceived the
kindest assistance and encouragement from Sir Joseph Hooker
and also the authorities of the Royal Gardens at Kew. ‘The
Delegates of the Oxford University Museum have kindly
given me access to their correspondence and minute-books.
II. On a new Stridulating-organ in Scorpions discovered by
W. J. Burchell in Brazil in 1828. By R. I. Pocock,
F.Z.S,
[Plate IV.]
UP to the present time stridulating-organs are known with
certainty to exist in three genera of scorpions, namely, the
Oriental genus Palamneus, the tropical African and Arabian
genus Pandinus, and the South-African Opisthophthalmus,
all belonging to the family Pandinide. ‘lhe certainty in
these cases lies in the fact that in both Palamneus and
Opisthophthalmus the hearing of the sound preceded the
anatomical investigation which led to the discovery of the
organ, and that in the species of Pandinus an organ exists
Stridulating-organ in. Scorpions. 57
exactly similar in structure to that of Palamneus, although
the rasp and the vibratile bristles occur upon different
segments of the chele and legs of the first pair in the two
genera. What is believed to be a stridulating-organ has also
been found in certain South-African species of the genus
Parabuthus, which belongs to a totally different family,
namely, the Buthidee. Unfortunately in this instance there
is no proof, based upon human perception of the sound emitted
by the living animal, that the function of the organ described
has been correctly interpreted. The tenability of the suppo-
sition, however, is justified by the structure of the organ and
by the distinctly audible stridulation it can be made to yield,
when the appropriate movements, all capable of being per-
formed by the animal itself, are induced by artificial means
on a freshly killed or aleohol-preserved specimen.
In the Pandinide the stridulating-organs have been deve-
loped in connexion with the anterior appendages. In Opisth-
ophthalmus it consists of large foliaceous bristles on the
inner (preaxial) surface of the basal segment of the cheli-
cere, and the sound given out by the rubbing of these
appendages together is in many cases supplemented by the
sound produced by the catching of certain short, erect, stiff
bristles on the dorsal side of this segment against the anterior
edge of the carapace as the appendages are forcibly withdrawn
beneath it.
In Pandinus and Palamneus it lies between the basal
segments of the appendages of the third and fourth pairs,
commonly called the chelze and first pair of legs, and consists
of a finely papillate area and an area beset with short erect
bristles exactly like those that are found upon the upperside
of the basal segment of the chelicerse in Opisthophthalmus *.
In Parabuthus what is supposed to be a stridulating-organ
is totally different both in structure and position. It is a
finely granular or transversely ridged area upon the dorsal
side of the first and second segments of the tail, possibly also
upon that of the last tergal plate of the abdomen, and the
stridulation above mentioned can be artificially produced by
scraping the point of the sting over the roughened field in
question. A fairly similar but less differentiated system of
granules, probably subserving the same end, is found upon
the first segment of the tail in certain black North-African
species of Buthus, namely, the Egyptian B., bicolor and the
Algerian B. eneas ft.
* See Pocock, Nat. Science, ix. pp. 17-25 (1896).
+ Pocock, Proc. Zool. Soc., March 1902, pp. 222-224.
} Pocock, Ann. & Mag. Nat. Hist. (7) x. p. 374 (1902).
58 Mr. R. J. Pocock on a new
Apart from the legs, which are almost immovably welded
by their basal segments to the sternal surface of the body,
the cheliceree, chele, and tail are, with one exception, the
only organs in a scorpion susceptible of vigorous and rapid
movement. ‘The one exception is the pectines. It is in
connexion with these appendages that the stridulating-organ
now to be described has been discovered *.
In the course of a recent study of Burchell’s manuscript
‘ Note-book of Brazilian Insects &c.,’ Protessor Poulton found
the following record under the date December 3rd, 1828 :—
1274, Scorpio of a light redish [thus] brown. Legs and
claws pale. Several of these were caught in my house. I
found one feeding on a large blatta which it held close to its
mouth with its claws. ‘ Laerdia.’ Makes a noise between
a hiss and a whistle, v. J. 31. 12. 28, with its pectiniform
appendages.”
The word “ Zacrdia”’ evidently represents the native
name of the species. Burchell always made a point of ob-
taining such names whenever possible, and took the greatest
pains in writing them clearly and inserting accents. The
reference “ v. J. 31.12. 28” apparently alludes to a Brazilian
journal which has unfortunately not been found. It certainly
did not reach either Oxford or Kew.
At once appreciating the interest and importance of the
last sentence of the note, Prof. Poulton arranged for the
collection to be searched for a scorpion bearing the number
1274. The specimen was soon found by Mr. W. Holland,
and Prof. Poulton brought it to the Natural History Museum
and asked me to determine it and to examine the pectines, to
discover if possible the nature and situation of the stridulating-
organ. This I undertook with the greatest pleasure, and with
the result that the accuracy of Burchell’s observation was
substantiated to the full.
‘The specimen is a male and belongs to the Brazilian species
that I described last year as Rhopalurus Borellu. Although
dried, it is sufficiently well preserved to preclude all likelihood
of error on this point ; but without the relaxation or removal
of the pectines the structure of the stridulating-organ could
not be investigated. The examination necessary for this
* Reference may here be made to the suggestion of Landois (‘Tierr-
stimmen, pp. 22-23, 1874), that the pectines might be capable of emitting
sounds by friction. ‘This idea, however, was not supported by facts, and,
except that the guess has now been verified, it is on a par with Wood-
Mason’s view that the prehensile teeth on the digits of the chele in
Buthide might also be used for this purpose (Proc. Ent. Soc. London,
1877, p. XIX).
Stridulating-organ in Scorpions. 59
purpose therefore was carried out upon the three spirit-
preserved examples the Museum possesses, namely, the type,
an adult female, an immature specimen of the same sex, and
an adult but badly preserved male.
Although only described seven months ago, this species
has been known to me for ten years. Briefly told, its history
and that of its allies is as follows:—In 1893 * I pointed out
that two American species of Buthide identified with the
Scorpio junceus of Herbst and Tityus agamemnon of C. Koch
differ from their allies in the structure of the pectines and of
the first sternal plate of the abdomen. The pectines are
unusually broad in their proximal half, and the overlying
area of the sternal plate is depressed, the grooves which
ordinarily pass forwards and inwards from the inner extre-
mity of the stigma being exceptionally deep and lying nearer
to the middle line, so that they define a narrow, smooth, tri-
angular area, standing at a higher level than the depressed
lateral portion already mentioned. On the strength of these
structural features the genas Heteroctenus was established for
these two species. It was also stated that Heteroctenus
Jjunceus differs from the form then referred to H. agamemnon
in having the depressed area smooth instead of closely and
finely but distinctly granular. Subsequently, as a result of
the publication of Dr. Kraepelin’s monograph + on the scor-
pions, it was found that these two species can scarcely be
separated generically from the species described as Rhopalurus
laticauda by Thorell and R. princeps by Karsch. Further-
more, the description given by Kraepelin, presumably from
an examination of the type of Tétyws agamemnon, proved my
previous determination of agamemnon to be erroneous. ‘f
therefore redescribed the species so determined under the new
name Borelliz}t, and at the same time attempted to show
that the five species under discussion—namely, junceus, lati-
cauda, princeps, agamemnon, and Borellii—possess certain
characters in common of sufficient systematic value to justify
their separation from the series forming the genus Centru-
roides, with which Kraepelin associated them, and to demand
their recognition as a distinct genus for which the name
fthopalurus is available §.
The significance of the depressed sternal areas and of the
expanded pectines in R. Borellii and R. junceus was always
* Journ. Linn. Soc., Zool. xxiv. p. 393.
t Das Tierr., Scorpiones et Pedipalpi, pp. 94-95 (1899).
t Ann. & Mag. Nat. Hist. (7) x. p. 375 (1902).
§ Biol. Centr.-Amer., Arachn. Scorp. p. 37 (1902).
60 Mr. R. I. Pocock on a new
a puzzle, and would probably have remained unsolved, so far
at least as I was concerned, had it not been for Burchell’s
until now unpublished discovery of three-quarters of a century
ago. Probably the absence of the granules on the depressed
sternal area in 2. junceus, suggesting as it did the secondary
importance of their association with the sternal depressions
and with the pectinal expansions in &. Borellii, coupled with
the flexibility, comparative softness, and known sexual
physiological significance of the pectines in these and all
other scorpions, combined to conceal the true construction,
which, thanks to Burchell’s observation, is now known to be
assignable to the features in question.
How, then, is the sound described by Burchell as ‘ between
a hiss and a whistle’’ produced? Without doubt by sweeping
the pectines across the granular field on the overlying sternal
plate (Pl. IV. fig. 2). When one of these organs is turned
over it may be noticed that the teeth opposabie to the granular
area are not parallel-sided, as is normally the case in scorpions;
the distal edge is sinuous, presenting towards the apex of the
tooth a very decided bulge, which shows up as a slightly
thickened area as it catches and reflects the light. When
examined under a half-inch objective, or even a lower power,
practically the entire face of the tooth, and especially the
bulging area, is seen to be covered with a multitude of fine
striz lying parallel to the longitudinal axis of the tooth
(PI.IV. fig. 3). That the structural modifications of the teeth
above described are directly connected with the depression and
granulation of the sternum is shown by the absence of such
modifications in the teeth at the distal end of the series which
lie beyond the granular area and sweep clear of it with the
movement of the pecten. No doubt the expansion of the
shaft of the pecten in its proximal half is correlated with an
increase in the size of its muscles and of the surfaces to
which they are attached to add force to the sweep of the
organ.
Except for the apparent absence of the granules, the sternal
depressions in J?. gunceus closely resemble those of &. Bo-
rellit. I originally described these depressions as smooth ;
this is only true relatively speaking. No granulation is
visible under a lens of low power, and no roughness is per-
ceptible with a pin-point ; but when scrutinized with a half-
inch objective the entire surface of the depression is seen to
be exceedingly minutely shagreened, so minutely as to suggest
that the sound emitted must be much finer than that
which the organ in 2. Borelli gives out. Nor is this all the
Stridulating-organ in Scorpions. 61
difference between the two species. The pectines in R. junceus
are expanded exactly as in &. Borellit, and the distal edges
of the teeth bulge in almost precisely the same way, but the
differentiation of the striz is carried to a greater extreme.
Along the edge of each tooth there is a distinct series of small
tubercular elevations, which are largest where they cross the
thickened bulging area, becoming smaller both above and
below it. These elevations are very distinctly striated, and
the strize appear to be practically restricted to them (PI. LV.
fig. 4).
In &. laticauda, Thor., the granules on the sternite are
relatively as coarse as in &. Borellii, but the area is less
depressed and less sharply differentiated both in front and
towards the middle line than in that species. Also the poste-
rior surfaces of the pectinal teeth are less visibly striated and
the distal edges of those opposable to the granular area are
straight and without the characteristic bulge so noticeable in
fh. Borellit and R. junceus. In all these features the organ
in &. latieauda is less specialized than in the two species just
mentioned.
The remaining species of Rhopalurus are unknown to me.
Those who have had the opportunity of seeing and describing
ft. princeps have made no mention of any structural peculi-
arities in the pectines or in the first abdominal sternuin.
According to Kraepelin, who has seen the typical examples,
however, this species is nearly related to R. laticaudu.
Hence it is permissible to suppose that it also possesses a
stridulating-organ suuilar in its general features to the stridu-
lator of that species. In the case of R. agamemnon the last-
mentioned author states that the pectines are expanded and
the sternum grooved and depressed as in R. junceus, but that
the sternum differs from that of R. junceus in being distinetly
granular on the medéan triangular area. This peculiarity, in
which R. agamemnon holds a unique position in the genus,
suggests that the median area in question constitutes an
integral part of the stridulating-organ. Whether the de-
pressed areas are granular or shagreened, or neither, is at
present unknown.
Two other important facts connected with Burchell’s
observation remain to be mentioned. ‘The first is the discovery
of stridulating-scorpions in America: those in which sounding-
organs are known or supposed to exist have hitherto been
recorded from the Mediterranean, Oriental, and Ethiopian
regions. The second is the announcement of the exact
locality of A. Borellit. R. princeps occurs in Hayti, R.junceus
62 Mr. E. 8. Russell on Depastrum cyathiforme.
in Cuba *, R. laticauda in Venezuela and Colombia, whereas
the only examples of 2. agamemnon and &. Borellit hitherto
known are labelled “ Brazil,” without further particulars.
Thanks, however, to Burchell, we are now aware that
R. Borellii is found in the Province of Goyaz, in the
upper valley of the Rio Tocantins or that of at least one of
its tributaries. Burchell was at Porto Real (now Porto
Nacional) when he made his note on specimen no. 1274,
Burchell’s collection also contains another specimen of the
same species (a female) bearing a label “ Body and legs
redish. Between the boxes at our station at Sape.
15. 10. 28.” Referring to the Index we find that Burchell
gives “ S? Brigida” as his locality on Oct. 15, 1828. Sapé
is mentioned on Oct. 14. The position is between Caval-
canti, his resting-place on Sept. 30th, and Conceig&o, which
he reached on Oct. 18th, but apparently much nearer to the
latter. A glance at Plate III. will show the positions of these
two localities of R. Borellit.
So far as the function of the organ in these American
Buthidee is concerned, it need only be said that since it is
equally well developed in both sexes, and occurs also in
immature forms, there is no reason to suppose that it has any
sexual significance. Hence, like the stridulating-organs of
other scorpions and of the spiders of the family Aviculariide,
its significance must be regarded as purely aposematic.
EXPLANATION OF PLATE IV.
Fig. 1. Rhopalurus Borelliit, Poc., 2, nat. size; drawn from typical
example.
Fig. 2. Ditto. Ventral surface of anterior extremity of abdomen and of
posterior extremity of cephalothorax, to show the granular
areas on the first abdominal sternite, the pecten of the left side
being removed.
Fig. 3. Ditto. Piece of the pecten seen from its dorsal side, to show the
finely ridged stridulating area.
Fig. 4. Rhopalurus junceus (Herbst). Ditto.
V.—Notes on Depastrum cyathiforme, Gosse.
By E. 8. RUssELL.
[Plate V.]
M. Sars, in 1846, was the first to describe and figure this
interesting little Lucernarian. He discovered it near Bergen
and described it under the name of Lucernarta cyathiformis
* There are specimens in the British Museum labelled “ Mexico” and
“Brazil.” These localities, however, require confirmation.
Mr. E. 8. Russell on Depastrum cyathiforme. 63
as follows :— Semipollicaris, stipite disco cireulari, repando
sese affigente; corpore cyathiformi, margine dilatata, repanda
circulari, integra (s. non in radios divisa) tentaculifera, ten-
taculis sepissime in fasciculis 8 fere continuis, ad marginem
corporis dispositis; organis generationis 8, binis approxi-
matis ” (Faun. lit. Norveg. no. 1, p. 26, tab. ii. figs. 8-13).
Shortly afterwards it was found in great abundance by
Mr. David Landsborough, Jun., at Southend, Arran, and
also by Dr. Landsborough at Corriegils, Arran. The
specimens were identified by Mr. Joshua Alder as Lucernaria
cyathiformis, Sars, and he sent a drawing to Mr. George
Johnston, who, on the strength of this drawing, incorporated
the species in his ‘ Hist. of Brit. Zoophytes,’ vol. i. p. 475
(London, 1847).
Gosse (Synopsis Brit. Actinie, 1858) then founded the
genus Depastrum for specimens which he found at Weymouth,
which he regarded as identical with the Lucernaria cyathi-
formis of Sars. Next year some small specimens were found
by Allman (Rep. Brit. Assoc. Aberdeen, 1859) in the Orkney
Isles, which seem to have been immature specimens of
Depastrum cyathiforme, Gosse. It does not appear to have
been recorded at any other locality until found by Beaumont
at Port Hrin, Isle of Man (‘ Fauna of Liverpool Bay,’ iv.:
Liverpool, 1895). He mentions also a specimen from
Plymouth.
In the month of July 1903 I rediscovered Depastrum on
the shore at West Bennan, Southend, Arran; and in
August, while at the Millport Biological Station, near the
Lion Rock, Millport, and also near the old castle on the east
side of Little Cumbrae. The animal seems to have a wide
distribution, and I have no doubt that a careful search
would reveal its presence in many localities from which it is
hitherto unrecorded.
I found Depastrum in large numbers under stones at
about half-tide, and also farther out. It adheres very firmly
to the underside or occasionally round the edges of fairly
large stones, so firmly that it has to be scraped off with a
knife. It is very local in its distribution, but generally
abundant where it does occur, though at one locality in
Little Cumbrae I found only a few scattered individuals. It
is difficult to account for its local distribution, but in my
experience it is never found in muddy localities nor in spots
where there is much decaying seaweed. It occurs well up
the beach, and appears to be quite a hardy form. In Arran
my largest specimens were got near low-water mark, but at
Cumbrae large specimens occurred more plentifully halfway
64 Mr. E. S. Russell on Depastrum cyathiforme.
up the beach. In its natural conditions it is almost always
pendent, being incapable of supporting itself with stalk
extended and erect, on the upperside of a stone. When
watched carefully in confinement it is seen to turn the widely
expanded bell-like umbrella in different directions, as if
searching for food. It appears to be quite incapable of
refixing itself after having been dislodged from its resting-
lace.
The stalk is very contractile, as is also the rim of the
umbrella. Four muscles, which extend up the teenioles
(Pl. V., tm.), are the agents for contracting the stalk, while
the margin is contracted by a circular muscle (em.) which
passes round outside the insertion of the tentacles, and in
contracting pulls the margin well over the tentacles, leaving
only a hole in the centre, through which the tips of some ot
the tentacles appear. I may here remark that it is only in
partly contracted individuals that several rows of tentacles are
seen; in fully expanded adult individuals there do not appear
to be more than two rows. Haeckel, in his diagnosis of this
species (‘ System der Medusen ’), describes it as having the
tentacles in severalrows. Furthermore, none of my specimens
reach the dimensions noted by Haeckel (8-10 mm. for
length of stalk, length of umbrella, and breadth of umbrella),
the largest I have seen having a stalk only 7 mm. long,
while the usual size of good-sized specimens is 4 mm. for
length of stalk, 6 mm. for height of bell, and 5-6 mm, for
breadth of same. ‘These specimens seemed mature, having
well-developed gonads.
‘There appear to be two forms of the species among my
specimens—one as figured, the other with a much sharper
distinction between stalk and umbrella, and with the breadth
of the umbrella as great as, or even greater than, the height
of the umbrella, ‘This latter seems to be the typical form,
for Haeckel describes the umbrella as being almost as high as
broad. ‘The measurements of a medium-sized individual of
this latter form are:—Length of stalk 3 mm.; height of
umbrella 4 mm; breadth of umbrella 4°83 mm. The smallest
specimen I possess measures respectively 1 mm., l*l mm.,
and 1:4 mm.
The sexes are distinct, but, so far as I can make out, indis-
tinguishable in external appearance. ‘lhe gonads are typically
in four double rows, but I have a specimen with only three
gonads and three lobes to the manubrium. Indeed, the
animal is very variable, especially as regards the number of
fascicles of secondary tentacles. The ova and spermatozoa
are very minute and very numerous. I attempted five times
ad
On a new Spider from Bounty Island. 65
in August to fertilize artificially, but failed each time, chiefly,
I believe, on account of the immaturity of the spermatozoa.
In the stomach of Depastrum I have noted the remains of
a small crustacean (probably a Copepod). When kept in
confinement unattached to a stone they sometimes void a
floccular mass, along with one or two phacelle, which looks
like a portion of the stomach epithelium. The tentacles also
are apt to slough off. It is very difficult to kill them well
expanded, but I have obtained good results by carefully
narcotizing with 30 °/, alcohol.
V1I.—On a new Genus of Spiders from Bounty Island, with
Remarks on a Species from New Zealand. By H. R.
Hoae, M.A., F.Z.8.
Proressor CHARLES CHILTON, of Canterbury College,
Christchurch, New Zealand, kindly sent me recently some
spiders obtained by Mr. L. Cockayne from the islands lying
to the east and south-east of the New Zealand coast. Among
these were some specimens found on the guano deposits of
Bounty Island, situated about 9 degrees east of Dunedin
(170° 30’ East longitude), between the better-known Anti-
podes and Chatham Islands.
The spiders belong to the family Agalenide, and the well-
developed colulus, front spinnerets close together, inner
margin of the falx-sheath toothed and sloping, with fringe
of incurved bristles on the outer, the upright maxille, and
square lip show them to belong to M. Simon’s group Cybeez.
Allied to the genus Emmenomma, Sim.*, this species differs
too materially to be included therein, so that 1 have formed a
new genus to receive it.
PACIFICANA, gen. nov.
Differs from Hmmenomma in having the cephalic part of
the cephalothorax convex and wide in front instead of not
convex and slightly attenuate. The thoracic fovea quite
short and shallow instead of long and deep. Rear row of
eyes so recurved as to form an area as long as broad instead
of about one half as long as broad. ‘Two teeth on inferior
* The single species for which M. Simon formed his genus Emme-
nomma was found on the islands adjacent to Cape Horn (about 67° W.
long.). The two localities are therefore separated by over 120 degrees of
longitude.
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 5
66 Mr. H. R. Hogg ona
margin of falx-sheath instead of three; three on superior
margin. About five pectinations on superior tarsal claws
instead of about nine.
The trochanters of all four pairs of legs are slightly but
clearly hollowed on the underside. This, with the mandibular
fringe and shape of lip and maxilla, breaks down the last
quotable distinction between the Agalenide, Pisauride, and
Lycosidee.
Pacificana Cockaynt, sp. n.
The colour of the cephalothorax is dark brown, the cephalic
part being bounded by a pale yellow marginal stripe. A
similar pale yellow area extends round the thoracic part
almost to the margin, where there is again a narrow streak
of brown. The mandibles are dark brown. Lip and maxille
paler brown, yellow on the outer edges of the latter. Sternum
pale brown on each side, with a longitudinal central yellow
streak. The legs and palpi are yellow, with brown rings,
one near the anterior end of the femur, one on the patella, two
on the tibia, two on the metatarsus, one at the anterior end of
the tarsus. In the front pair the whole of the tarsus and
metatarsus is brown. ‘The abdomen on the upperside has a
series of transverse scolloped stripes yellow and black alter-
nately. The underside is greyish yellow.
The shape of the cephalothoraz is a long oval, truncate at
the slightly narrowed anterior end. ‘The cephalic part is
considerably raised above the thoracic; a short, shallow,
longitudinal fovea extends from behind the cephalic part to,
but not down, the rear slope.
The pattern of the eyes is quite unique. The front laterals
are large, one and a half diameters apart, and one third of
their diameter from the margin of the clypeus. Four small
intermediate eyes one fourth of the diameter of the above are
situated between them at the corners of a trapezium, the rear
pair, their diameter apart, slightly above the line joining the
upper edges of the laterals; the lower pair, rather farther
apart, are below the line touching the lower part of the laterals.
The lateral eyes of the rear row, rather more than their
diameter apart, are about three fifths the diameter of the front
laterals and the diameter of the latter away from their own
median. Thesmall front median eyes are their diameter from
the margin of the clypeus.
The mandibles are nearly twice as long as the front
patelle, much kneed at the base, and taper to the anterior
end, the fangs being rather long, slightly curved, smooth for
the first half and striated longitudinally the second. ‘The
new Spider from Bounty Island. 67
falx-sheath is sloping and has two teeth on the inner margin
near the upper end. ‘here are three teeth below the fringe
of bristles on the outer margin, the middle one being the
largest.
The mawille are upright, convex, rounded in front, and
broadest near the anterior end. The dip longer than broad,
on a narrowed base, is rounded at the sides and broadly
truncate in front.
Pacificana Cockayni.
a, eyes, X 10; 4, spider, nat. size; ¢, epigyne, x 10.
The sternum is nearly twice as long as broad, truncate in
front, and running to a point posteriorly.
The abdomen is oval, sparsely covered with short fine hairs,
The spinnerets two-jointed, tapering, the second joint quite
short. ‘Lhe inferior pair close together, the colulus broad and
long.
The legs are moderately stout, the metatarsal and tarsal
joints tapering to a rather fine point. ‘The superior tarsal
claws have about five pectinations at the basal end only, the
Re
68 Mr. H. R. Hogg on a
inferior claw being smooth. At the anterior end of the meta-
tarsi is a ring of short incurved spines and four pairs of
spines on the underside of the front two pairs. The tarsi are
without spines.
There is a longitudinal seam along the front side of the
coxze, and the chitinous margin of the trochanters is slightly
hollowed on the underside, the species in this respect, asin the
mandibular fringe, approaching the Lycoside.
The measurements () in millimetres are as follows :—
Long. Broad.
Cephalothorax.... 95 3} in front.
Abdomen... sn: 12 63
Mandibles ...... 4
Tr. & Pat. & Metat.
Coxe. fem. tib. & tars.
DGERS saute sivas Cassans il 3 7 8 7 = 25
2. 22 63 64 6 = 213
2 9 6. «5k CSR =
4, 23 iy 8 7 = 244
MAR wtb seretots sc a ekeodae 23 3} 3t 3 = 12
There are one male (unfortunately wanting a moult) and
four females.
From Wanganui, North Island of New Zealand, Mr. W.
Gray was so good as to send me two small pieces of moss-
covered bark, each a few inches square. On my first examina-
tion I could see no reason of adequate interest to account for
their having been sent so long a journey by post. It was
only after careful search that I found the lids of no less than
five nests of a little Migas spider, apparently that first
described by L. Koch, MZ. paradoxus.
The doors of the nests fitted so closely, and, although com-
posed of woven felt, so exactly resembled the adjoining bark
and lichen as to be quite invisible on a casual inspection.
The occupant of one nest had come out and was unhappily
crushed, but the other four nests contained live females, one
in each. The nests are little silken sacs wedged between
interstices of the bark, about ? inch in depth and 2 inch across
the opening.
In the collection made by the ‘Challenger’ expedition,
recently returned to the British Museum (Natural History)
after a prolonged absence, is another specimen from Wellington,
evidently the same.
Spider from New Zealand. 69
The legs in all the specimens are rather longer in propor-
tion to the cephalothorax than the measurements given by
L. Koch, but they agree closely otherwise with his description
of his type specimen from Auckland, and I have no reason
to doubt their being the same, more especially as the legs are
normally carried closely bent up and are not easy to measure.
As in all this group, the tarsi and metatarsi of the front
two pairs of legs are flattened and abnormally short. The
metatarsi are furnished with a double row of stout curved
spines on the underside (in my paper, Proc. Zool. Soc. Lond.
1901, ii. p. 229, by a misprint this character is ascribed to
metatarsus iv.).
The superior tarsal claws have one long pectination, with a
few uneven rugations on either side.
The front row of eyes is straight, the rear row is slightly
recurved,
Migas paradoxus, L. Koch.
a, eyes, X 10; 4, profile, nat. size,
The cephalothorax and mandibles are yellow-brown ;
sternum, lip, and maxille yellow ; abdomen black and rather
rugose above, dark yellowish grey below. The space in
front of the genital aperture and spinnerets yellow.
The strongly recurved cephalic fovea and rather profuse
bespining of lip and maxille (in female) are marked features.
I append measurements (in mm.) of one of Mr. Gray’s
specimens, apparently adult, and of the still larger ‘Challenger’
specimen :—
Specimen from nest (W. Gray).
Long. Broad.
Cephalothorax.... 33 25 in front.
3k
Abdomen,.,.....- 1 3
Mandibles ...... 4 hor’. 2vert’.
70 Mr. H. Schwann on new Forms of
Tr. & Pat. & Metat.
Coxe. fem. tib. & tars.
1
LUGO oo beri vane Le = 33 33 DE 103
9, 1k 31 3h 1. f= 000
3. 1 oT ee re i
4, at gts ON Se Tog er a
125 eR ae ale eae 14 22 13 1] = i
‘ Challenger’ Expedition specimen.
Long. Broad.
Cephalothorax.... 5 33 in front.
z
Abdomen erect 6 41
Mandibles ...... 2hor’. 33 vert’.
Tr. & Pat. & Metat.
Coxe. fem. tib. & tars.
Meosye iets newts ] 2 5 43 3 = 143
2 1} 4; 4 9: ‘= 198
3 ee ee ee ee
4 9 42 4a 18} = 6 1G
Pal pl otitis Sele 05 a. oiris iz 3 23 a 3
Migas distinctus, Cambr., from the South Island, described
as having a pattern of yellow spots on the back and having
more widely separated eyes, will no doubt be distinct from
the above; but Mr. Goyen’s Migas Sandageri, from Moko-
hinou Islands, near Auckland, now that we know he means
recurved by bent forward, would seem from his description to
agree exactly with M. paradowus of L. Koch. Mr. Goyen
found the nests of M. distinctus in clay-banks; those of
M. paradoxus and M. Sandagert are on the trunks of trees.
It is interesting to note that M. Simon has found the nests of
the allied South-African Moggridgea to be built both in the
ground and on bark.
VII.—On new Forms of Anomalurus and Sciurus from
Tropical Africa. By HAROLD SCHWANN.
AN examination of some of the more recent African accessions
to the British Museum collection which I have been enabled
to make with Mr. Thomas’s permission shows that the
following forms require description.
Anomalurus Beecrofti argenteus, subsp. n.
General colour above silvery grey, more or less suffused
with yellowish towards the middle line; basal portion of the
Anomalurus and Sciurus from Tropical Africa. 71
hairs on the flanks darker than those on the body, producing
an indistinct dark patch on the edge of the membrane ; general
colour of uader surface dirty grey; throat strongly suffused
with “ orange-rufous,’ passing into pinkish buff on the
stomach and hind limbs; head silvery grey, cheeks and lower
jaw silvery white, a white patch on the crown between the
ears and a white band running along the shoulders; under-
part of forearms and sides of stomach dirty white ; outer edge
of membrane on upper surface behind forearms covered with
stiff black hairs extending backwards for about 14 inches ;
tail dirty grey.
Dimensions of the type (measured in skin) :—
Head and body about 385 mm.; tail 139; hind foot
(s. u.) 41.
Skull: greatest breadth 36; length of upper tooth-
series 12°5,
flab. Abutschi, River Niger, about 150 miles from the coast.
Wiyjpe. b.M.' no. 2. 11; 10, 7. Collected, Feb. 1902 by.
A. J. Braham, Esq.
This subspecies differs very considerably from the type of
Anomalurus Beecrofti from Fernando Po described by Fraser
both in general colour and skull-measurements. The latter,
however, in this group are so variable, even among members
of the same species, as to be of little value. As an example
two adult specimens, both undoubtedly Anomalurus Beecrofti,
differed by as much as 1°5 mm. in the length of the upper
tooth-series. In colour A. B. argenteus differs from Anoma-
lurus Beecrofti in being of a light silvery grey on its upper
surface instead of ‘ yellowish grey.” It is also much less
suffused with rufous on its under surface.
Sciurus rufobrachiatus ruwenzori, subsp. n.
Altied to S. keniea, Neum.*, but with a certain amount of
fulvous on its muzzle and feet and a pure white streak on the
under surface.
General colour above “ olivaceous,” the hairs brown,
speckled with ‘ochraceous,’ without the marked rufous
suffusion found in S. nyanse. Base of the hairs “ slate-
grey.” Length of the underfur about 15 mm. and of the
long hairs 25 mm. Under surface “creamy buff,” not
sharply detined, gradually passing into the “olivaceous” of
the sides. Middle line of under surface with a sharply defined
white streak about $ inch broad extending from the inter-
ramia to the inguinal region, its hairs white to their bases.
* SB. Ges. nat. Fr. Berlin, 1902, p. 176.
12 On new Forms of Anomalurus and Sciurus. -
Top of muzzle dull fulvous, passing into “ olivaceous” on
the crown. Cheeks and upper surfaces of the feet and fore-
arms grizzled yellowish. Hairs of tail annulated with black
and buffy yellow. :
Dimensions of the type (measured in the skin) :—
Hind foot (s. u.) 51 mm.
Skull: greatest length 52; basilar length 40°5; greatest
breadth 29°5 ; length of upper tooth-series 9.
Hab. Wimi Valley, Ruwenzori. Alt. 2400 m.
Type. Adult male. B.M. no. 95. 3. 5. 2. Collected
6th July, 1894, by G. F. Scott Elhot, Esq.
In colour this subspecies is intermediate between S. r. ny-
ans and S. kenie, having less fulvous on the muzzle and
limbs than the former and more than the latter.
Sciurus rufobrachiatus pasha, subsp. n.
Fur hardly so thick or so long as that of S. r. nyanse ;
length of long hairs on back about 21 mm. and of underfur 11.
General colour above dark brownish, rather warmer than
Ridgway’s “ bistre”’; base of the hairs slaty black. Flanks
distinctly lighter than back; base of hairs “ slate-grey.”
Under surface very thinly covered with creamy-white hairs,
interspersed with a few black ones. Difference in colour
between flanks and belly unusually conspicuous, with the
line of demarcation well defined. An indistinct white patch
on throat and chest, hardly constituting a streak. Top of
muzzle and round orbits dull orange-buff. Fore and hind
feet and outer side of forearms rich ‘ ochraceous rufous.”
Underside of thighs and lower limbs sparsely covered with
whitish-buffy hairs. ‘Tail like back for its basal two inches,
the remainder annulated with black and dirty white.
Dimensions of the type (measured in the skin) :—
Head and body 249 mm. ; tail 234; hind foot (s. u.) 49.
Skull: greatest length (c.) 50; basilar length 39; greatest
breadth 31°5 ; length of upper tooth-series 10.
Hab. Bellima, Monbuttu.
Type. Adult male. B.M. no. 87. 12. 1. 31. Collected
13th July, 1883, and presented by Dr. Emin Pasha.
This subspecies, allied to S. 7. nyanse, is more strongly
suffused with rufous on the back and base of tail, while it is
of a much lighter colour on the feet and belly. S. kaffensis,
O. Neumann *, from the other side of the Nile, differs by
‘« die schéne rostfarbene”’ annulation of the caudal hairs. It
may be mentioned that an allied form from Southern Nigeria
* Op. cit. p. 57.
On new Lycenide from Sierra Leone. 73
is also remarkable for the almost naked condition of its under
surface, but is distinguishable by the absence of any rufous
colour on the limbs.
The four members of the S. rufobrachiatus group found in
Central and Central East Africa may be distinguished as
follows :—
A. Fulvous or reddish on muzzle and feet.
a. A marked white streak along under surface .... S. 7, rutvenzorit.
6. No white streak along under surface.
a’. Underside of forearms and thighs deep rufous
colour ; belly well haired, dull buffy ...... S. 7. nyanse.
6’. Underside of thighs with no rufous suffusion ;
belly thinly covered with whitish-grey hairs. S. 7. pasha.
B. No fulvous colouring on feet or muzzle ......... . SS. kenie.
VIIL.— On new Species of Lycenide from Sierra Leone.
By D. Cator.
I FEEL pretty sure that the Pseuderesie here described are
not the only new ones that I have lately discovered, but I
await further material, which I hope to find before very long.
They need a deal of hunting, as their haunts are in shady
places and they are most difficult to capture on the wing—
firstly, because of their sombre colouring on the underside and
the small amount of colour above, so that they can be seen
only at intervals whilst flying; and, secondly, because if not
taken at the first attempt they will not probably give another
opportunity, as they easily take fright. If, however, they
can be seen at rest they can easily be caught if they are not
too high up, but they need much looking for; they rest on
twigs and creepers bare of leaves, but, excepting one or two
species, seem to be distinctly uncommon.
Pseuderesia Bakeriana, sp. n.
3 .— Upperside. Fore wings black, outer margin faintly
scalloped, inner margin up to beyond vein 1 orange from near
the base to beyond the middle: hind wings orange, with very
broad black posterior borders decreasing rapidly towards
costa. Underside. Both wings greyish black, hind wings
rather the paler of the two: fore wings with red irrorations
on the costa, a squarish red patch on the costa beyond the
cell, which is confluent with the red irroration up to the
74 Mr. D. Cator on new
posterior margin and which broadly occupies the whole of that
margin; in this marginal red irroration is a short black
macular stripe, lower part of cell and below vein 4 to inner
margin spotless and paler: hind wings with three interrupted
irregular transverse reddish stripes, bordering the third a
broad blackish band, edged exteriorly by a band of fine
reddish irrorations, beyond which is another dark band,
followed again by fine reddish irrorations to the margin ;
fringes white, intersected with blackish.
9. Upperside. Both wings orange: fore wings distinctly
more rounded than in male; costal edge, base, cell and
rather beyond irregularly black, apex very broadly, outer
margin broadly black: hind wings like the male. Underside.
Fore wings (with outline of pattern as above) orange, fading
into yellowish on the inner margin ; costa blackish, three
dark spots in the cell and one larger beyond it; apex very
broadly finely irrorated with reddish on a blackish ground ;
outer margin similarly irrorated, but less broadly: hind
wings like the male, but paler and without reddish.
Exp. wings, ¢ 31-33, 2? 30-32 mm.
I have much pleasure in naming this after my friend
Mr. G. 'T. Bethune-Baker, who has assisted me so much in
working out my captures. Found so far in March, April,
May, and October, but probably flies from October to May,
which covers the dry season in Sierra Leone.
Pseuderesia nigra, sp. n.
$.—Upperside. Both wings entirely black, with white
fringes tessellated with black. Underside. Fore wings black,
shading into dark greyish on the inner margin; traces of
three black spots in the cell, with a red one between the
second and third; apex darkly spotted, in front of which is
an oblique row of four red spots, two being below the apex
and two on the posterior margin: hind wings grey, of a
peculiar texture, the wing having the appearance of having
been denuded of scales, with various black and red spots;
the base of the wing is suffused with red, with a small black
spot palely encircled below the costal vein near the base; in
the cell are two black spots, palely edged, the small one at
the base and the other large, directly below which is another
large black one; on the costa is a large black patch reaching
to the upper angle of the cell, beyond and touching which is
a red irregular spot; transverse stripe from apex to inner
margin very decided, composed of a black-spotted stripe edged
externally by an equally decided red-spotted stripe, the two
Lycenide from Sterra Leone. 75
central spots in each being confluent and very large, margin
spotted with a black Junular stripe; the ground has a suffusion
of red beyond and below the cell; all the red spots are very
bright, approaching vermilion.
? .—Upperside. Both wings bright ochreous: fore wings
with costa broadly dark brown, very broadly dark brown
from the end of the cell and tapering down the posterior
margin to the anal angle; cell with three spots in it and
several below; ground-colour snffused with brown below the
cell almost to the inner margin; fringes brown, intersected
with white: hind wings with costa broadly brown, posterior
margin very broadly dark brown, increasing in width from
the apex to the inner margin, base suffused with brown;
fringes intersected with white. Underside. Fore wings pale
orange, base suffused with blackish ; costa blackish, cell with
three spots, increasing in size, and one below the cell touching
the second and third cell-spots ; apex as in the male, but the
oblique orange spots are preceded by a very broad blackish
band: hind wings ochreous grey, with pattern as in the male,
only the red spots are replaced by orange ones.
Exp. wings, ¢ 34, 2? 30 mm.
This species may prove to be a subspecies of P. vardegata,
S. & K., but it is a beautiful and striking form. Besides the
types described above, I have one male with a small orange
patch on the upperside of the fore wing. Caught in February
and April.
Pseuderesia fusca, sp. n.
$.—Upperside. Fore wings black, with white fringes
intersected with black: hind wings black, with an orange-
coloured costa increasing in width from the base to below the
apex on the outer margin ; fringes whitish, intersected finely
with black. Underside. Fore wings dark grey, with a small
black dash closing the cell and asmall black spot at the origin
of vein 2; beyond the cell a curved transverse row of small
blackish spots, followed by a similar more obscure submarginal
row: hind wings ochreous brown, witha small dark spot near
the base below the costal vein, followed by three small oblique
dark spots—one below the costa, one closing the cell, and
one below the cell; beyond the cell is a transverse, fine, inter-
rupted, blackish macular stripe from the costa to the internal
vein, beyond which is the rather obscure posterior marginal
row of blackish dots ; margin finely dark.
¢ — Upperside. Both wings black: fore wings with a
broad orange-yellow patch a third from the base on the inner
margin to near the outer angle, extending obliquely across
76 Bibliographical Notices.
the wing to above vein 4, where it suddenly narrows and is
inversely oblique to the costa: hind wings like those of the
male, but not so dark. Underside. Ochreous grey, inner
marginal area of fore wings yellowish ; pattern asin the male,
but rather more distinct, owing to the lighter ground-colour.
Exp. wings, ¢ 27-29, 2 26-28 mm.
Liptena albicans, sp. n.
Upperside. Both wings white: fore wings with the costal
half slightly tinged with cream-colour ; costa finely blackish
(rather wider near the base), apical area rather broadly dark
grey to black at extreme apex: hind wings with fringe cream-
coloured. Underside. Both wings whitish, slightly cream-
coloured: fore wings have costa to costal vein pale orange-
yellow, continued finely to the apex; on the costa close to
the apex are three dark dots or lines, which, however, are not
always present; outer margin orange-yellow, edged internally
finely with black, intersected at the veins as far as vein 3, the
fringe of this part also being black, inner marginal area pure
white: hind wings with the posterior margin very finely
cream-coloured, edged internally by a fine black line; fringes
whitish.
Exp. wings 29-31 mm.
This species is near L. decipiens, Kirby, but the underside
of the wings has no trace of any marginal band at all. It
very often flies high among the trees, settling occasionally,
and not, as arule, moving faraway. JF oundin March, April,
and June.
BIBLIOGRAPHICAL NOTICES.
Catalogue of the Collection of Birds’ Eggs in the British Museum
(Natural History). Vol. II. By Everne W. Oares and Capt.
Savite G. Rer. London: Printed by Order of the Trustees of
the British Museum. 1903.
Tuer present volume contains brief descriptions of the eggs of 907
species, ranging from the Parrots to the Bulbuls (Pycnonotide).
Though the greater part of the book had been written by
Mr. Oates, he was, owing to protracted ill-health, obliged to relin-
quish the work, a fact which we must all deplore. The Museum,
however, is fortunate in having secured the services of Capt. Savile
Reid for the completion of the remaining volumes.
Bibliographical Notices. (a
No change has been made in the method of treatment, which, as
we have already remarked, seems to us wanting in fulness and to
miss a great opportunity for suggestive generalizations. Perchance
Capt. Reid may be induced to give us a general summary on the
study of oology in the last volume. Nowhere is the need for such
a summary so well exemplified as in the case of the treatment of
the eggs of the Common Cuckoo.
This volume is illustrated by ten coloured plates, remarkable for
their extreme beauty. The selection of the figures has obviously
been most carefully made.
The Geological Structure of Monzoni and Fassa. By Marie M.
OetiviE Gorpoy, D.Se., Ph.D, 1902-03[1903]. 8yvo. 180 pages,
with 14 photographs, 33 figures, 4 geological sections (black and
white), 8 geological sections (coloured), 1 table of stratigraphical
succession, 1 coloured geological map, and 1 reference contour
and fault map. Edinburgh: Turnbull and Speers. London:
Simpkin, Marshall, & Co.
Tis memoir is a ‘Special Part” of Vol. viii. of the ‘Transactions
of the Edinburgh Geological Society,’ published in 1903. The
date of “1902” on the titlepage refers to the year when it was read
before the Royal Society, as stated in the Prefatory Note. According
to the generally accepted bibliographical and nomenclatorial rules
only the date of publication can be taken for the chronological
status of a book. An abstract: having been printed elsewhere, the
Royal Society, by its rules, could not itself print the paper.
The Alpine Range, as a whole, is well known as a region that
has been subjected to repeated movements ; and, indeed, it cannot be
positively said that the cracks in the rocks and their displacements
are even now in a state of absolute equilibrium. In the South
Tyrol the elevated areas of Triassic strata, rugged and precipitous,
are characterized by more or less isolated, rudely columnar or
sharply peaked mountains, which have long been objects of wonder
to the tourist and of study to the Geologist. To the former it has
attractions in its picturesque aspects; but, if his reflections reach
farther and deeper than the common notions of mystery and romance
among the bizarre cliffs, peaks, and gorges, he may well desire to
know the “ why and wherefore” of their real history and outcome.
This country has for a long time been carefully examined by many
Continental Geologists, to whose published observations and de-
scriptions Miss Ogilvie (afterwards Mrs. Ogilvie Gordon) has referred
in several papers. Attention had, however, been especially drawn
to the fossils of Saint Cassian &c. Difficulties, however, were found
in determining the relationships of the strata and the fossils. Of
late years the lady-student above mentioned directed her energies
to the elucidation of the doubts and difficulties which seemed
hitherto to be beyond solution. Aided and guided especially by the
advice of Baron yon Richthofen among her Continental and of
78 Bibliographical Notices.
Professor Lapworth among her British friends, Mrs. Ogilvie Gordon,
D.Se., Ph.D., entered more fully into her projected work in the Tyrol.
After hard field-work, making important contributions to our know-
ledge of Alpine Geology, both as to the arrangement of strata and the
occurrence of fossils, she completed in 1901 the excellent geological
map which accompanies the paper before us. This brilliant and
solid geological work has been steadily continued and improved by
the same lady, asshown by hercontributions to scientific periodicals *,
with elaborate and trustworthy descriptions of the region in explana-
tion of its complex structure.
In these researches Dr. Ogilvie Gordon has always kept in touch
with the Continental Geologists working at the same problems.
The Triassic masses in this region consist largely of Dolomites ;
and these are said by the Author to be isolated by faults. Folded
by many successive creeping movements of the Earth’s crust, inter-
sected by slip-faults and thrust-faults, they have also suffered much
by local subsidences, and by repeated cross-faultings, with shear-
planes and their crush-breccias.
The outlines of the mountains in some places have been likened
to that of upraised coral-reefs; and, if really such, the dolomite
condition would not be strange, for it is known that corals become
dolomitized. Careful scrutiny, however, detects fossiliferous strati-
fication in some of the dolomite masses, but whether due to shells
or to beds (not reefs) of Coral on bases of calciferous Algals is not
settled.
Both volcanic and deep-seated igneous rock-matter play important
parts in the make-up and physical character of the country. The
igneous magma has come up to the fissures of weakness in the various
rocks, either to spread out on the top or to lose itself in the cross-
cracks or in the side-planes and cleavage-lines. They take the
Geologist far afield in his science in finding and explaining the
origin, material, age, and mode of passage of the different veins,
dykes, and sills. Some of the intrusions appear to have been of an
age previous to the Triassic, some to have been contemporaneous
with it, and some decidedly to be of later (Tertiary) date.
The following is given in a Table opposite page 19, in this “ Special
Part ” of vol. viii. Trans. Geol. Soc. Edinburgh [1903], as the succes-
sion of the Triassic formations in the South Tyrol :—
Urrer TrIAs.
About 370 métres, | Dachstein Limestone or Dolomite. 320 métres.
in the vicinity of { Raibl Marls, &e. 50 métres.
Fassa.
Deen ee aan
* Especially the ‘Geological Magazine,’ 1892, pp. 145, 147, and 381,
382; Quart. Journ. Geol. Soc. vol. xlix. 1893, pp. 1-77; Geol. Mag. 1894,
pp-1-10 and 50-60 ; Q. J. G.S. vol. lv. 1899, pp.663-634; Geol. Mag. 1902,
pp- 809-317 ; and, lastly, Trans. Edinb, Geol. Soc. 1908, vol. viii. “Special
Part,” pp: 1-179.
Bibliographical Notices. 79
(Schlern Dolomite or Dolomitic Limestone (including at
| the base the Clpit Limestone). 350 métres.
Mipptz Trias. } Cassian Marls. Bolraeirs
About 510 meétres. 1 Wengen Shales, Tuffs, &c. Des ean
| Buchenstein Limestones. 20-40 métres.
| Mendola Limestone or Dolomite. 40-60 metres.
( Passage-beds. Crinoid Limestone, Oolites, and Rauch-
wackes. 60-90 métres.
Upper Werfen Marls and marly Limestone. Naticedla
costata zone. 100-160 métres.
Lower Trias. Blue shales and marls. 35 métres.
About 500 métres. { Micaceous layers or Rauchwackes. 25 métres.
(maximum). Lower Werfen. Redand grey marls and shales, Pseudo-
monotis Clarat zone. 130 métres.
Lingula tenuissima zone. 20 métres.
Poikilitic marls and limestone. Natica gregaria zone,
G 40 métres.
Pantin Bellerophon Limestone, gypsum, &e.
ed 70 RAairGs Gréden Sandstones, Quartzites, or Breccias.
* | Quartz-porphyry.
It is indicated also in this Table :—That the Schlern, Cassian, and
Wengen beds are equivalent to Salomon’s ‘“* Marmolite Limestone.”
That the Mendola limestone and the Passage-beds are equivalent to
Salomon’s ‘‘Alpiner Muschelkalk.” That “the Passage-beds are the
age-equivalent of the uppermost horizons of the ‘ Myophoria beds’ or
‘Reichenhall Limestone’ in the North Tyrol and Bavaria-Roth
horizon with salt, gypsum, &c.” The Upper Werfen is equivalent
to Richthofen’s ‘“Campil Strata” and the Lower Werfen to his
“ Seisser Strata.”
The numerous fossils collected by the Author in the field, except
the Wengen-Cassian fossils of Sella Pass (pages 26-28) were almost
all from the Werfen series, and were identified for her by Dr. Broili,
of Munich.
The igneous rocks received great attention from the Author in
the field and have been carefully described, from her preparations,
by Mr. Gibb, of Aberdeen; and to indicate the important part
played by them in nature and described in this Memoir, we may
with advantage quote the following from pages 29-30 :—
“This paper therefore confirms the conclusion I previously formed when I
investigated Enneberg and Buchenstein, viz., that the copious flows of augite-
porphyrite, regarded as extrusive were in reality intrusive, and had been
intruded pre-eminently into fault-planes and lines or horizons of weakness and
crust-deformation. The previous investigators of Fassa Valley failed to
recognise the presence of the innumerable crush-planes with extremely low
hade, and the branch-connection of many of them with leading cross-faults, and
consequently overlooked the correlation of the igneous invasions with pre-
existent deformational structures.
« As the presence of igneous rock undergoing consolidation amidst the Triassic
successicn only served to still farther accentuate and concentrate the differential
strains at special horizons of the crust, during the Tertiary movements thesame
crush-zones were again and again the seat of crush-movements, and were
invaded afresh by molten material. In the immediate vicinity of the Jarger
igneous masses, the sedimentary deposits tended to subside; thus the local
80 Miscellaneous.
horizontal crust-strains increased in intensity. During protracted periods of
crush and deformation, the earlier intrusions suffered, together with the
original thrust-masses and dowuslip-slices. They were cleaved and faulted,
locally altered, sheared or fragmented just as their sedimentary roof and floor.
Later dykes and veins ramified in them and in the environing sediments, and
the direction of these later dykes often gives valuable evidence of the local
horizontal crust-strains associated with continued local subsidences.”
And at pages 13-14 of the Introduction it is conclusively stated
that
“In the Fassa and Monzoni district there are the same evidences as in the
Sella country of cross-folding and cross-thrusting. But now I furnish a mass
of new evidence to show how greatly extended in time these movements were,
how extremely complex their deformational effects, and how essentially the
history of intermittent intercalations of igneous material was knit up with a
long history of local subsidences taking place within the Periadriatic region of
the Alps'and producing effects which inevitably interfered with the movements
of Alpine distribution.”
MISCELLANEOUS.
A Correction to “ Notes on some Meduse from Japan.”
By R. Kirxearrick, F.Z.S,
In a short paper entitled ‘“ Notes on some Meduse from Japan,”
published in the ‘ Annals’ for December 1903, I gave an account
(p. 616) of a Medusa which I thought belonged to an undescribed
genus and species, and to which I applied the names ‘“ Grono-
meandrus chrysostephanus.” This Medusa, however, was described
and figured by Tilesius in 1818 (Mém. Acad. Sci. St. Pétersbourg,
1818, tom. vi. p. 554, pl. xviii.) under the name Medusa saltatrox
(from Nagasaki).
Haeckel (‘ System der Medusen,’ Zweiter Nachtrag, p. 636) places
Tilesius’s species under Polyorchis, though he had, in manuscript,
referred it to a new genus, Spirocodon.
In 1886 Goette (Sitzungsber. Akad. Wiss. Berlin, 1886, xxxix.
p. 832) refers this species to the genus Spirocodon, Haeckel, and
places the latter in a new subfamily, Sprrocodontide, between the
subfamilies Polyorchide and Berenicide of the family Cannotide.
I am much indebted to Mr. E. T. Browne for suggesting that the
specimen described by me was the Medusa saltatriw of Tilesius and
for calling my attention to the above-mentioned references to the
literature on the subject.
As there has been no figure of Spirocodon saltatriv since the
“ eidliche Abbildung” published by Tilesius in 1818, I trust that
the carefully drawn figures of Mr. Highley, published in connexion
with my notes, will prove of interest.
Ann .de Mag. Not. Hist.S.7 Vol. XULPLL.
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DEPASTRUM CYATHIFORME, Gosse.
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st. Secondary _,, g. Gonads.
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THE ANNALS
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]
No. 74. FEBRUARY 1904.
IX.—WNotes on Mantide tn the Collection of the British
Museum (Natural History), South Kensington, with Descrip-
tions of new Species. By W. F. Kirsy, F.L.S., F.E.S.
THE undescribed species of Mantide in the National Collec-
tion are not very numerous; but I here describe a series of
interesting forms in advance of my ‘ Catalogue of Orthoptera.’
It is proposed to include the Gressorial Orthoptera (Forficu-
lidee, Hemimeridee, Blattidee, Mantide, and Phasmide) in the
first volume, leaving the Saltatorial groups (Gryllide, Phasgo-
nuride, and Locustidz) to be included in the second volume.
Mantide.
EREMIAPHILINE.
Genus THEOPOMPA, Stal.
Theopompa Westwoodi, sp. n.
Exp. al. 75-102 mm.
Femalee—Head pink, mouth-parts paler; eyes and ocelli
very prominent; a strong transverse ridge on the face just
below the antenne.
Prothorax dark reddish brown above, sides and under
surface paler; an angular projection on each side in front,
though the prothorax attains its greatest width further back,
at about one third of its length, after which it narrows
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 6
82 Mr. W. F. Kirby on Mantidee in the
gradually towards the extremity. Sides of mesothorax above
and upper surface of metathorax and abdomen mostly black,
or interalary spaces and base of abdomen pruinose blue;
the under surface, the extreme tip of the abdomen, and the
appendages pale.
Front legs bone-colour or pale flesh-colour, with most of
the spines tipped with black ; coxe conspicuously pale and
marked with two small black spots above; femora with the
outer side longitudinally excavated and strongly granulated
on the basal half, and edged below towards the tip with three
strong spines ; the inner surface edged with numerous spines ;
ridged in the middle and longitudinally excavated above ;
below the ridge a long black basal blotch runs nearly to the
middle; beyond this the ridge is marked with an interrupted
black line, and there is another rounded black blotch below it
before the extremity. Middle and hind legs flesh-colour,
spotted with darker.
Tegmina hyaline, with pink nervures on the costal and
internal areas and on the disk ; otherwise pink, varied with
darker at the base, below the anterior radial, and along the
other principal nervures ; there are about six oblong spots on
the basal third of the anterior radial, which is branched at its
extremity ; the upper branch of the posterior radial forms a
short wide fork at the extremity, most distinct on the right
side.
Wings brownish hyaline, darker towards the costa at the
base, and the costal and apical areas varied with lighter and
darker spaces ; the branches of the anterior ulnar vein long.
The male is much smaller than the female and less pink,
with the basal half of the wings brownish.
Hab. Ashanti; Tamsoo, Gold Coast.
Allied to J’. heterochroa, Gerst., but larger, the wings
lighter, more uniform in colour, and differently veined.
Genus HUMBERTIELLA, Sauss.
Humbertiella ocularis.
Q. Humbertiella ocularis, Sauss. Mém. Soc. Genéve, xxiii. p. 16 (1872).
Exp. al. 46 mm.
Male.—Body and legs reddish above, testaceous beneath.
Head and prothorax more or less varied with black above ;
legs spotted and streaked with black above, the black and
testaceous markings forming long alternate streaks on the
middle and hind tibie and tarsi.
Tegmina of a slightly yellowish hyaline ; a row of oblong
black spots along the mediastinal nervure, the rest (except
Collection of the British Museum. 83
the costal and internal areas) marked all over with round
brown spots along the nervures. Wings brownish hyaline,
with obsolete brown spots towards the tips.
Hab. Borneo.
Resembles H. indica, Sauss., 3, but in that species the
spots are much smaller, linear, and do not extend to the
wings, and the abdomen is much darker above. It must
also much resemble the male of H. ceylonica, Sauss.
Humbertiella (?) Brunnert, sp. n.
Entella Brunnert, Fruhstorfer, MS.
¢o .—Long. corp. 21, exp. al. 25 mm.
? .—Long. corp. 25, exp. al. 28 mm.
Clay-colour, more or less mottled with light brown; head
and pronotum without conspicuous elevations ; pronotum with
the shoulders rounded off, but otherwise with the outline
nearly as in H. indica.
Tegmina reddish, with yellowish nervures, frequently
expanded, especially in the female, into indistinct spots; the
subcostal nervure with a black line more or less broken into
long spots. A large somewhat ill-defined pale stigma,
bordered before and behind with blackish; the anal area and
nearly the half of the lower and outer border almost trans-
parent. Wings dark orange towards the base in the male,
more reddish towards the costa ; a broad smoky-brown border,
intersected by white transverse nervures ; above the fold the
border is narrower, darker, and slightly edged with hyaline
at the extreme apex of the wing. ‘The female differs in the
basal part of the wing being bright yellow, with no reddish
shade.
Hab. Lombok.
This curious species seems to me to be more nearly related
to Humbertiella than to Entella or to Hapalomantis, to which
Westwood refers a Bornean species (H. semirufula), the
female of which (Rev. Mant. pl. 1. fig. 1) appears to be nearly
related to our Humbertiella Brunnert, except that the extre-
mity of the pronotum is distinctly narrowed in the figure.
Genus PyrGoMANTIS, Gerst.
Pyrgomantis Jonesi, sp. n.
Long. corp. 45, exp. al. 55 mm.
Male.—Yellowish brown or light brown (perhaps green
during life); tegmina and wings with the costal area
yellowish ; smoky brown towards the base, with the transverse
6
84 Mr. W. F. Kirby on Mantidee tn the
nervures mostly white below the middle; outer part of wings
and tegmina smoky hyaline.
Hab. South Nigeria (Dr. S. A. Jones).
Resembles P. singularis, Gerst. (which I cannot distinguish
from P. nasuta, Thunb. & Sauss.), but easily recognizable
by the coloured wings and by the protuberance on the head,
which is broader and more obtuse.
Cu@RADODINZE.
Genus CHa@rADODIS, Gerv.
Cheradodis squilla.
Cheradodis squilla, Sauss. Mitth. schweiz. ent. Ges. iii. p. 72 (1871) ;
Mém. Soe. Genéve, xxi. p. 18, pl. iv. figs. 3, 3. (1871).
Hab. Ceylon.
The insects figured by Westwood as C. squilla agree with
O. cancellata, Fabr., as identified by Wood-Mason, and not
with the former species.
Mantinz.
Genus HAPALOPEZA, Stal.
Flapalopeza maculata, sp. n.
Long. corp. cum tegm. 20 mm.
Yellowish green (probably green during life) ; face with
two round black spots below the ocelli, and two larger ones on
the vertex ; behind these, two, wider apart, being just within
the eyes, and between these are two other small reddish spots,
and low down on the occiput are two more black spots.
Antenne black, with the first and third joints pale. Pro-
notum greenish in the middle and reddish on the sides, with
four large black spots, two on the widest part and two before
these. Legs greenish, the knees, tips of spines, and tips of
tibiz and tarsi darker; front femora with two small reddish
or brownish marks on the basal half.
Tegmina subhyaline, strongly iridescent, with the subcostal
nervure reddish; the other nervures mostly brown.
Hab. Ceylon (E. E. Green).
Allied to H. tigrina, Westw., which is possibly not distinet
from H. nitens, Sauss. Some specimens of HH. maculata are
more reddish and uniform in colour than that described, with
the spots on the head much smaller and less distinct; but
the four large spots on the pronotum and the two small spots
on the front femora seem to be always constant.
Collection of the British Museum. 85
Genus CARVILIA, Stal.
Carvilia costalis, sp. ne
Mantis cincta, var, a, Gerst. Decken’s Reisen in Ost-Afrika, ili, (2)
pp. 14, 15 (1873).
Long. corp. 52, exp. al. 50 mm.
Female.—Tawny brown; head with the base of the labrum
black, and a black oval transverse depression, on the lower
edge of which the two upper ocelli stand; head transverse,
twice as broad as the front of the prothorax.
Prothorax half as long again as the meso- and metathorax
taken together ; suddenly expanded above the anterior coxa,
the frontal lobe carinated and granulated above, and the whole
length of the prothorax set with rather small teeth on the
sides.
Abdomen expanded, colour darker than the rest of the
body.
Front legs testaceous; coxe granulated and denticulated
behind, and edged in front with a row of about 15 small teeth,
of which 4 or 5 are larger than the others, and are black
beneath, except at the tips. Coxe marked with three blackish
bands above, and below with a spot at the base, and a large
dusky space before the extremity. Femora with 3 strong
teeth on the upper edge and about 12 on the lower, the latter
black beneath. ‘Tibize with about 14 spines, those towards
the extremity black at the tips, and the terminal spine wholly
black ; on the upper and outer surface the femora are marked
with three blackish bands.
All the tarsi blackish ; middle and hind legs otherwise dull
reddish, with no distinct markings.
Tegmina blue-black, with traces of a pale transverse band
across the centre ; costal area yellowish, and the apex and
hind margin tawny brown; hind wings blue-black, the
margins paler, and the costa narrowly reddish.
Hab. Abyssinia.
Gerstaecker may be right in treating this insect as a variety
of his M. cincta, but it is very different in appearance from
the typical form of that species.
Genus SPHENDALE, Stal.
Sphendale xanthoptera.
Mantis xanthoptera, Oliv. Enc. Méth. vii. p. 637. n. 61 (1792).
Mantis ochroptera, Licht. Trans. Linn. Soc. Lond. vi. p. 29. n. 29
(1802).
Mantis nympha, Stoll, Spectres, Mantes, p. 19, pl. i. fig. 22 (1813).
The locality of Stoll’s specimen is given as Negapatam.
86 Mr. W. F. Kirby on Mantidee zn the
A female from Nepal, fairly agreeing with his figure, was
ticketed Mantis obscura, Fabr., by Bates; but the type of the
latter species is a male, and came from “ Equatorial Africa ”
(probably Sierra Leone).
Sphendale robusta, sp. n.
Thespis robusta, Bates, MS.
Long. corp. 63, prothor. 17, exp. al. 39 mm.
Female.—Brown, front legs slightly marbled with black ;
tegmina unicolorous, except the internal area, which is blue-
black, except at the base; wings with the costal area
yellowish, with a black spot in the middle; otherwise light
violet-brown, with white cross-nervures. .
Hab. Nepal.
Closely allied to S. wanthoptera, Oliv., but the front coxe
and the sides of the prothorax are much more finely denticu-
lated, the prothorax is slightly and the abdomen considerably
broader, and the tegmina and wings are much more uniform
in colour.
Genus Puotina, Burm.
Photina gracilipes, n. n.
Cardioptera reticulata, Sauss. Mém. Mex., Mant. p. 196 (1871), nec
Burm.
Hab. Para (?).
Saussure has enumerated two species under the name of
Cardioptera reticulata, and Westwood has renamed Bur-
meister’s species Mantis Burmeisteri (Rev. Mant. p. 15). But
in such a case it is the second species, not the first, which
requires another name.
Genus LEPTOCOLA, Gerst.
Leptocola gracillima.
Leptocola gracillima, Gerst. Mitth. Ver. Neu-Vorpommern, xiv. p. 92
(1883).
Euchomena Stanleyana, Westw. Rey. Mant. p. 33 (1889).
This curious species occurs in various parts of Western
Africa, from the Cameroons to the Congo.
Collection of the British Museum. 87
VaATINz.
Genus Hererocua£ra, Westw.
(Are. Ent. i. p. 161, pl. xli., 1845.)
Heterocheta orientalis, sp. n.
Long. corp. 115, long. pronot. 50, exp. al. 120 mm.
General colour reddish grey ; head deeply concave in front,
semicircular, the vertex forming a narrow transverse carina,
at least in the female, and the eyes curving outwards and
forwards, very large, and ending in a large conical spine.
Pronotum narrowed in front and strongly granulated, carinated,
laterally serrated before the enlargement above the coxe,
which is moderate, and bordered by a narrow rounded ridge.
Hind part of prothorax with a middle carina and distinctly
raised at theextremity. Front coxa minutely serrated above
and very strongly and irregularly dentated below, but more
strongly in the female than in the male. ‘Two teeth near the
base and one before the extremity are the largest. Middle
and hind femora with small dentated lobes at the extremity
beneath.
Tegmina varied with reddish, and subhyaline grey, the
yeddish colour increasing and becoming more uniform towards
the extremity ; inner margin hyaline. Wings on the costal
area almost hyaline, with transverse dark spots ; apex yellow,
preceded by a large steel-blue blotch. The rest of the wing
is clear subhyaline yellow, divided by narrow undulating
steel-blue bands in the male, which are broader and anasto-
mose in the female.
Hab. Luitpoldhette, East Africa (¢); German Kast
Africa (2); British East Africa (immature 3).
It is probably this species to which Gerstaecker alludes
(Mitth. Ver. Neu-Vorpomm. xiv. p. 94, 1883) as a variety of
the very distinct West-African LH. tenudpes, Westw.
Genus PSEUDOCH ATA, nov.
Allied to Heterocheta, Westw.; eyes shorter, obtusely
conical, and ending in a blunt point instead of a long spine ;
ocelli very prominent ; middle and hind femora with rounded
denticulated lateral lobes ; cerci jointed and laminated.
88 On Mantide in the British Museum.
Pseudocheta Strachant, sp. 0.
Long. corp. 114, prothor. 36, cercorum 8, exp. al. 103 mm.
Female.—Body and legs shining fawn-colour, the latter
indistinctly mottled with darker; prothorax with the dorsal
carina well marked; laterally denticulated throughout and
slightly expanded above the front coxe ; front coxe slightly
curved, attenuated beyond the middle, and slightly expanded
again before the extremity ; dorsal and lateral carinze finely
denticulated, the front lateral carina with about 6 mode-
rately large teeth ; front femora half as long again, attenuated
and distinctly curved beyond the middle, with long pale spines
tipped with black, and the lower carina denticulated to the
base; front tibie slender, not more than half as long as the
femora, with only 6 spines on the outer carina, including the
terminal one, but with a great number of curving spines on
the inner carina, gradually increasing in length, and termi-
nating in an immense curving hook about two fifths as long as
the tibie. First joint of the tarsi slender, curved, about half as
long as the tibize and two fifths longer than the remaining joints
of the tarsi. Middle femora and tibie rather short (especially
the femora) and attenuated in the middle ; all the carine very
finely denticulated ; femora with an inner and tibie with an
outer terminal spine. Hind femora and tibie long, rather
slender, of nearly equal length, and all the carine very finely
denticulated ; femora with an inner terminal spine, tibie
with an inner and outer one.
Tegmina subhyaline, clouded with fawn-colour on the
costal half; wings subhyaline, clouded with pink along the
costa, below which are several rows of light brown and sub-
hyaline blotches, and towards the centre the wing is orna-
mented with large irregular spots and bands of lighter yellow
and steel-blue.
Abdominal lamin slightly narrowed at the base, otherwise
uniformly broad, and obtuse at the ends.
Hab. Lagos (Dr. Strachan).
This very interesting species has a strong superficial
resemblance to SHeterocheta ortentalis from Hast Africa,
described above.
On Malacodermata from South Africa and Brazil. 89
X.—The Collections of William John Burchell, DCL, tn
the Hope Department, Oxford University Museum.
III. Rhipidocérides et Malacodermes recueillis par W. J.
Burchell dans ses voyages en Afrique australe (1810-
1815) e¢ au Bréstl (1825-1830) ; avec la description de
quaire espéces nouvelles. Par J. BOURGEOIS.
I HAVE added to Mons. Bourgeois’ memoir all the observations
and data I can find recorded in Burchell’s manuscript notes.
Such additions are placed between square brackets. The
numbers by which the specimens are brought into relation
with the present series of papers are printed in heavy type,
to distinguish them from Burchell’s reference numbers.—
E. B. Poutron, Dec. 9, 1903, Oxford.
RHIPIDOCERIDZ.,
RHIPIDOCERA, Latr.
1. marginata, Kirby, 1 ¢.—Brésil.
[No. 215. Sept. 15, 1825, Rio. Burchell went for an excur-
sion on this day “along the Aqueduct (from Sta. Theresa to
the ridge above the valley of Laranjeiros),” but the words in
his “ Notes of Brazilian insects’ probably indicate that he
captured the insect in the house at Rio. “ Lampyris. Non
lucet. Caught in my room; perhaps brought in with the
plants.”’]
MALACODERMATA.
Lycida.
Lycus, Fabr.
Lycus in sp.
2. ampliatus, Fahr., 1 g.—Afrique australe.
[The specimen is numbered 82. The corresponding number
in Burchell’s manuscript “ Catalogus systematicus Insectorum
in Itinere per Africam australem extratropicam” proves that
the insect was captured on March 12, 1814, “in plantis” at
Wagenbooms River, north of Plettenberg Bay. Burchell was
in much uncertainty as to the determination of the species.
He gives thenames “‘rostratus g, Fab.,” with an inverted query,
90 Mons. J. Bourgeois on Malacodermata
“TJ, palliatus ex verb. Lichtens[tein].” He also added
the word “new’’ in pencil, and suggested the specific name
“ scutatus, B.,” underlining it according to his custom. The
specimen was also examined by Dr. W. E. Leach, of the
British Museum, as is proved by a paper in his handwriting,
dated by Burchell Nov. 28, 1818. This manuscript, which
is bound into the “ Catalogus,” is a letter and list of the
numbers upon over one hundred forms of Burchell’s South-
African insects, with determinations or such statements as
‘new,’ “ unknown,” “ not described,” ‘ to be examined,” &e.
The letter speaks of other lists to follow “next week,” but
no more have yet been found. A postscript says “ Do send
me on Monday by post your names for the new species ” [see
above, pp. 48, 49]. In nearly fifty cases such suggested names
were written by Burchell in Leach’s list. No. 82 is stated
to be “ new or not described,” and the name “ scutatus”’ is
written opposite to the number here as in the “ Catalogus.”
“1 Duplicate L.” indicates that one specimen was given to
Leach for the British Museum. ‘The letters “?S. L.” in the
“Catalogus” indicate that Burchell thought, but was not
sure, that the species 82 also occurred at Sierra Leone, to
use his own words, “ according to a small collection sent to
the Horticultural Society, and which I saw at the Linnean
Society, 2. 8. 22.”
There are three other references to no. 82 in Burchell’s
handwriting :—
(1) A series of notes headed ‘‘ The following notes are the
result of a collation of the whole of my African collection of
insects, with the Banksian Cabinet (now belonging to the
Linnean Society), the greatest part of which is named in the
handwriting of Fabricius. 1823 to 1824” ; and then, appa-
rently added later, “but I fear some labels had been
misplaced.” In this list we find “82. Lycus rostratus ¢.
Specimina Banksiana sunt pauld minora.”
(2) Another undated collation headed “ The following
Notes are the result of a collation of all my African insects
with the figures in Olivier’s ‘ Entomologie.’”’ Here we find
“ 82. Lycus latissimus.”’
(3) The third reference is on a single sheet in Burchell’s
handwriting, headed “ Remarks on my African Insects by
Mr. Wm. McLeay, 1 April, 1824.” McLeay’s opinion, as
recorded by Burchell, was “ all the Lyc/are distinct species.” ]
3. palliatus, F., var. pallulatus, Dalm., 1 g.—Afrique austr.
[No. 81. Nov. 18, 1813, Uitenhage, Cape Colony. ]
Jrom South Africa and Brazil. 91
Chlamydolycus, Bourg.
4-9. Burchelli, sp.n.,3 3,3 ?.—Afrique australe.
[All captured at Uitenhage, Cape Colony, Nov. 18, 1813.]
3. Breviter ovatus, fere opacus, supra ochraceus, thoracis disco
(limbo antico excepto), elytrorum regione scutellari, macula
magna laterali ad expansionem elytrorum, sutura trienteque
apicali nigris; subtus niger, nitidiusculus, abdominis lateribus
ochraceis ; rostro breviore quam in Z, elevato; prothorace trans-
verso, subtrapeziformi, basi longitudine fere duplo latiore, apicem
versus parum attenuato, antice subrotundato, lateribus medio
paululum coarctatis, medio longitudinaliter sat profunde sulcato,
angulis posticis extus vix productis, apice retusis; elytris in
dimidio anteriori singulatim in expansionem magnam, supra con-
cavatam et valde reflexam, infra autem conyexam et declivem
rotundato-dilatatis, dein ad apicem singulatim rotundatis, fortiter
reticulatis, intervallis reticuli grosse rugoso-punctatis, costis 2
parum elevatis instructis ; abdominis segmento penultimo postice
in medio paululum triangulariter inciso, ultimo (8°) elongato-
triangulari, bivalvato, omnino nigro; pedibus nigris, trochanteri-
bus femorumque basi (tertii paris preecipue) plus minusve rufes-
centibus.
Long. 10-13 mill.; lat. max. thorac, 24~4 mill.; lat. max. elytr.
8-11 mill.
2. A mare differt elytris subparallelis, expansione elytrorum ad
laminam elongatam, angustissimam, immaculatam redacta ; abdo-
minis segmento ultimo (7°) semilunato, integro.
Long. 10-14 mill. ; lat. 6-8 mill.
Trés voisin de L. Poulton?, Bourg. (Ann. Soe. ent. Fr.
1902, p. 739) ; en différe surtout par la taille moindre, le rostre
un peu plus court, le milieu de l’abdomen noir dans les deux
sexes (chez Poultont g abdomen est entiérement ocracé) et
par l’expansion humérale de la 9 A peine marquée, réduite
une lame trés peu saillante et allongée, d’ot résultent, dans ce
sexe, des élytres presque paralléles.
[The females are numbered 78 [7], 79 [8], and 80 [9].
The numbers in brackets are those of the specimens in the
present paper. No. 78 was submitted to Leach and marked
‘not described,” the name oblongus, B., being suggested by
Burchell both here and in the “ Catalogus,”’ where “ new”? is
written in pencil. In the Banksian Collation Burchell wrote
opposite 78-80 “ L. proboscidens? [Fab.] qui figuram habet
elytrorum apice majus angustatam.” In the Olivier Collation
the same name is given to no. 80. The ‘ Catalogus”’ men-
tions “5 duplicates” and a single “ L.,” indicating that one
specimen was given to the British Museum.
92 Mons. J. Bourgeois on Malacodermata
The males are numbered 86 [4] and 87 [5], and one bears
the date 18. 11. 13 [6] without a number. No information
is to be found concerning these three specimens, except the
locality and date and the fact that there were “4 duplic. L.”]
Merolycus, Bourg.
10, 11. rostratus, L., 2 g.—Afr. austr. [Uitenhage, Cape
Colony, Jan. 16, 1814.]
12. , var. pyriformis, Murray, 1 g.—Afr. austr.
[Burchell’s no. 85 captured at the same date and locality as
10 and 11. “ Mares gaudent elytris latioribus.—Fcem. an-
eustiorib. Vix volantem vidi. Hab. in floribus ” (Catalogus).
In the Banksian Collation Burchell wrote ‘85. Lycus.
Similis colore forma Lyco rostrato qui tamen abunde differt
rostro, et elytris paulo majoribus.’’]
CALOPTERON, Guér.-Mén.
13. tropicum, L. (fasciatum, F.), var. humeris immaculatis,
¢.—Brésil. [Porto Real (now Porto Nacional),
March 3, 1829.]
Le type de V’espéce a les élytres tachées de jaune aux
épaules et parait plus spécialement répandu en Guyane; j’en
al vu cependant plusieurs exemplaires du Brésil.
14-17. brasiliense, Cast. (sinuaticolle, Luc.). Color. typic. :
elytris fusco-nigris, macula humerali magna fasciaque
lata transversa pone medium flavis ; abdominis segmentis
primis medio flavo-maculatis (Bourg. Comptes Rend.
Soc. ent. Belg. 1879, p. xv). 14,3 2.
[The male [14] bears the number 808, indicating capture,
Oct. 22, 1825, on the excursion from Rio into Minas Geraés.
The detailed locality is given as “ In a Roca (about 4 miles
S.S.W. of the house of Discoberto) on the road towards
Nepomucena.” The single specimen captured is named
“ Lycus.” The dates and localities of the other specimens
are respectively :—[15] Feb. 9, 1826, by the River Pacaqué,
Organ Mountains; [16] Feb. 21, 1826, Organ Mountains ;
and [17] Jan.15, 1827, Cubatao, “ given by Thomas Smith.” ]
18, 19. , var. a: elytris flavis, fascia dorsali interrupta
apiceque late nigrescentibus (Bourg. loc. supr. cit. p. Xvi).
2 ?.—Brésil, Cubatao.
[18. Dec. 8, 1826. “ Cubatao, at the Rio das Pedras at
from South Africa and Brazil. 93
the Citio (where I resided) at the foot of the ascent up the
great range of mountains.”
19. Jan. 15, 1827. “ At Rio das Pedras and Cubatio.”]
20. brasiliense, var. y: elytris fusco-nigris, fascia transversa
obsoleta, sepius interrupta pone medium flava, humeris
vix flavescentibus ; abdomine omnino nigro (Bourg. loc.
supr. cit. p. xvi). 1 ?.—Brésil.
[Nov. 2, 1825. Excursion into Minas Geraés, “ at Fran-
cisco Manoel’s.’’|
91. serratum, L., 1 ¢ .—Brésil.
[The specimen bears the date “ 2?. 6. 29.” On June 2,
1829, Burchell was at “ Sitio das Pedras,” on the Rio
Tocantins, a little above Para.]
99, limbatum, F., var. affine, Luc. (nec Taschenb.), 1 ¢.—
Brésil, Cubatao.
- [Dec. 8, 1826. See no. 18.]
93. seavittatum, Taschenb., Giebel’s Zeits. 1874, p.96. 1 ¢.
—Brésil, Organ Mountains.
[Feb. 15, 1826. “ Along the road 14 mile S. of the
house.” Evidently near the River Pacaqué in the Organ
Mountains. ]
CELETES, Newm.
94, Burchelli, sp. n., 1 g .—Brésil, Cubatio.
¢. Elongatus, subparallelus, sat dense tenuiter pubescens, vix
nitidus; capite brunneo, mandibulis palpisque testaceis, eculis
maximis, valde prominentibus, nigris ; fronte concavata ; antennis
brunneis, articulo secundo minimo, transverso, testaceo, sequenti-
bus, a tertio inde, flabellum compressum, articulum ipsum longi-
tudine multo superantem, a basi emittentibus, ultimo compresso,
elongato-elliptico, preecedente duplo longiori ; prothorace trapezi-
formi, parum transverso, antice attenuato, medio longitudinaliter
carinato, ochraceo-flavo, disco fuscescente, margine antico medio
angulato-lobato et utrinque sinuato, lateribus sat coarctatis, angulis
anticis bene distinctis, posticis extrorsum valde productis, apice
subacutis ; scutello subquadrato ; elytris basi latitudine thoracis,
apicem versus paululum dilatatis, subparallelis, brunneis, humeris
fasciaque transversa mediana ad marginem dilatata ochraceo-flavis,
4-costatis, costis 2 et 4 multo elevatioribus, intervallis costarum a
94 Mons. J. Bourgeois on Malacodermata
celathris transversis quadrato-areolatis; corpore subtus brunneo,
trochanteribus femorumque summa basi genubusque flavescentibus.
Long. 6 mill. ; lat. 2 mill.
[Captured at 10 P.M. on Dec. 18, 1826, between the
* Middle Part of the ascent up the”’ Sierra da Cubat&io and
the “ Upper Part” of the same ascent. |
PLATEROS, Bourg.
29. apicalis, Germ.,.1 ex.—Brésil, Minas Geraés, near Nepo-
mucena.
[Nov. 8-6, 1825. See above, page 45. On 3rd and 4th at
Francisco Manoel’s, 5th at Jofio Alfonso’s, 6th at Capit&o
Leite’s. ‘On the 3rd took a stroll up the hill to a Roea and
got many insects.” “4th .... ascended the hill into the
forest northward of our Rancho and took insects, till wet
through in a thunder shower. In the evening caught some
insects by the candle.’’]
26. variicostatus, sp. n., 1 9 .—Brésil, Minas Geraés.
? ) D]
Subparallelus, supra fere planatus, subopacus, tenuissime pubescens,
nigro-fuscus, prothorace antice et lateraliter sat late flavo-mar-
ginato, trapeziformi, basi longitudine paullo latiore, antice sub-
rotundato, basi utrinque sinuato, lateribus fere rectis, angulis
anticis sat bene distinctis, posticis extrorsum versus paulum pro-
longatis, subacutis, disco postice longitudinaliter canaliculato,
antice carinulato; elytris 9-costatis, costis inequalibus, alternis
(presertim 4, 6 et 8) magis elevatis, sexta a medio inde attenuata,
intervallis costarum a clathris transversis punctato-areolatis ;
corpore subtus nitidiusculo, tenuiter pubescente, fusco, trochan-
teribus femorumque summa basi rufescentibus; abdominis seg-
mento ultimo ogivali (9 ).
Long. 7 mill. ; lat. 23 mill.
Espéce voisine de P. inequalis, Bourg. (Ann. Soc. ent. Fr.
1899, p. 99), mais de coloration différente.
[Oct. 28, 1825. “ Lampyris.” At Discoberto, Minas
Geraés. ]
Lampyridide.
Hyas, Cast.
27. Sp.?, 1 2 .—Brésil, Minas Geraés.
[Oct. 21, 1825. “ Lampyris.” “In a rossa at Disco-
berto and along a channel (on the margin of the forest) which
conducts water to the house.” ]
Jrom South Africa and Brazil. 95
CLADODES, Solier.
28. lamellicornis, Mots., 1 g¢.—Brésil, Rio.
(Jan. 1, 1826. “ Catéte and Prdia de Flaméngo.]
AXTHRA, Cast.
29. maledicta, Kirn. Oliv., Ann. Soc. ent. Fr. 1888, p. 79
(lateralis, Cast., nec Guér.-Ménev.). 1 ¢.—Brésil,
Cubatao,
[Dec. 9, 1826. ‘ At Rio das Pédras ; in the Forest.’’]
Luciporta, Cast.
30. Sp. ?, 1 ex.—Brésil, Minas Geraés.
[“ Lampyris.” Oct. 25, 1825. “ At Discoberto, near
Joao Pedro’s house.” ]
31. Sp. ?, 1 ex.—Brésil, Minas Geraés.
[‘ Lampyris.” Oct. 16, 1825. On the previous day
Burchell was “at the Discoberto do Antonio Velho.’’]
PuHoTINuS, Cast.
32. Sp. ?, 1 ex.—Brésil, Minas Geraés.
[‘ Lampyris.” Oct. 16, 1825. See no. 81.]
33. Sp. ?, 1 ex.—Brésil, Organ Mountains.
[Feb. 12, 1826. “By the River Pacaqué.”]
34. Sp.?, 1 ex.—Brésil, 8. Paulo.
[June 19, 1827. ]
35, 36. Sp.?, 2 ex.—Brésil, Minas Geraés.
[‘‘ Lampyris.” Oct. 13, 1825. On Oct. 12 Burchell was
at Parahita.]
CRATOMORPHUS, Mots.
37-40. giganteus, Drury, 4 ex.—Brésil, Cubatio.
[1826 [87], Dec. 6, “ at Mr. Eric Smith’s sitio at Rio das
Pédras”; [88] 7 P.M. Dec. 7th, probably the same locality ;
[89, 40] Dec. 10, ‘‘ Rio das Pédras,” 2 examples. ]
96 Mons. J. Bourgeois on Malacodermata
41. ? concolor, Perty, 1 ex.—Brésil, Pard.
[Jan. 25, 1830.]
ASPIDOSOMA, Cast.
49-52. lineatum, Schénh., 11 ex., dont I’un avec la mention
manuscrite: “luce intermittente.””—Brésil.
[The dates and localities of the specimens are as follows :—
42,43. Dec. 29, 1825 (2 examples). From Rio de
Janeiro to Catombi, Barra Vermélha, and Rio Comprido.
44, Jan. 26,1826. Riode J. “ A botanical and entomo-
logical excursion to the Barra Vermélha, Morro de Ladeira,
and Catombi.”
45. April 19, 1829. Porto Redl (now Porto Nacional).
46. June d3;'. ,, Pard.
AY, Aug! 2h. Pard, 8. José.
48. Sept.1, ,, * : [ arsenal).
AQ. Sept. 2, 4, 5 is (between 8S. José and
5O--Sept. 19; 5; 35 %
51. Nov. 14, ~,, a ys
52. Jan. 11, 1830. Pard. ‘ Luce intermittente.’’]
53. ?cassidewm, Mots., 1 ex.—Brésil.
[Pard, Jan. 21, 1830, 9 P.M. |
54. ? dmpressipenne, Mots., 1 ex.—Brésil.
[Feb. 11, 1826. Organ Mountains, “in a walk to the Ipé
trees.’”|
55. Sp.?—Brésil.
(Santos, Sept. 28, 1826, 7 P.M.]
56-61. roseiceps, Bourg., Revue d’Entom. 1884, p. 286 (décrit
par erreur de Nouvelle-Calédonie).—Brésil, 6 ex.
[56. Jan. 1, 1826. Rio. Catéte and Prdia de Flaméngo.
57. Sept. 20, 1826. Santos. In the Forest above the
Monastery of 8. Bento. ‘ Lampyris: the common sort
flying in the evenings: and its larva, also giving fits of
light.” One of these larvee [57 4] captured by Burchell on
the same day, Sept. 20, is also in the collection.
58, 59, 60. Sept. 28, 1826, 7 p.m. (3 examples). Santos.
61. Nov. 26, 1826. Santos.
from South Africa and Brazil. 97
57 a. Cette larve rappelle, par sa forme générale, celle de
l’Aspidosoma candelarium, Reiche, décrite et figurée par
Goureau dans les ‘Annales de la Société entomologique de
France,’ 1845, pl. 7. ii. figs. 1-6; mais elle en différe
(autant, du moins, qu’il est permis d’en juger sur un exem-
plaire piqué et déja vieux) par le premier arceau thoracique
un peu plus allongé et plus atténué en avant, ainsi que par
les 2° et 3° plus grands, sensiblement plus longs que les
suivants. Les tubercules stigmatiféres des cétés des segments
abdominaux ne sont pas saillants comme dans la figure citée
ci- dessus, mais cela tient sans doute a l’état de dessication de
cette larve. Quant aux pattes, elles sont conformées de
méme, frangées de quelques soies a leur bord interne et
terminées par un double crochet.—Long. 9 mill.; larg. max.
22 mill.]
62. Sp. ?—Brésil.
[Rio, aqueduct. March 12, 1826.]
63. Sp. ?—Brésil, Minas Geraés.
[Oct. 25, 1825. At Discoberto, near Jo&o Pedro’s house.
« Lampyris?”’]
Lampyris, L.
64-66. Sp.?, 3 g.—Afrique australe. LZ. conspicuce, Gyll.,
vicinus, sed scutello abdomineque flavis.
[No. 88 [66], “ 13 Duplic. LL,” was captured at 7.30 P.M.
on Oct. 6, 1814, at Nowsakamma River, Mossel Bay.
‘‘Abdominis pars alba lucem reddit. v. J.” (Catalogus).
The reference is evidently to an undiscovered Journal of
South-African travel. Leach considered the species new, and
Burchell suggested the name wliginaria, B., for it, but in
his Banksian Collation doubtfully sets it down as “ Lampyris
marginata 3.”
No. 92 [64], “6. Dupl. L L,” was captured at 8 P.M. on
Oct. 3, 1814, at Sylvan Station, north of Georgetown.
Leach considered it as possibly the same form as that figured
by Olivier (“pl. i. f. 56?”), and Burchell suggested the
name “ sylvatica, B.”’ In his Olivier Collation Burchell noted
the same resemblance as follows :—“92. Lampyris mauri-=
tanica quoad figuram (Genus 28, Tab. i. fig. 5 6) sed fig. 5a
est valde diversa.”
The third specimen [65] bears only the date 3. 10. 14
(when Burchell was at “ Sylvan Station”’), with the figure 7
and an imperfect letter, which probably indicates P.[M.].]
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 7
98 Mons. J. Bourgeois on Malacodermata
AMYTHETES, Illig.
67-71. apical’s, Germ., 5 §.—Brésil, Rio de J.
[Sept. 15, 1825. Along the Aqueduct (from Sta. Therésa
to the ridge above the valley of Laranjeiros). Five specimens
are mentioned in the “ notes,” with the following remarks :—
“ Lampyris (Lycus), Antenne uno latere latissime pectinate
nigre. Elytr. rufescentia, apicibus nigris. Ex sylvaticis
herbosis. Noctu valde lucens.’’]
72. Sp.?, 1 ¢.—Brésil, Pard.
[ Dec. 15, 1829, 12 p.m. ]
MEGALOPHTHALMUS, Gray.
93-78. ptiliniformis, sp. n.,6 g.—Brésil, Pard.
3. Oblongus, pallide fusco-griseus, flavido pubescens ; capite fusco,
mandibulis palpisque testaceis; oculis nigris; antennis articulo
primo flavo, sequentibus infuscatis, ramulis pallidis, immaculatis ;
prothorace rugoso-punctato, transverso, trapezoidali, margine
antico leviter rotundato, lateribus fere rectis, subparallelis, basi
sat profunde bisinuata, angulis posticis leviter productis, disco
infuseato, levissime carinulato, pone medium tuberculis 2 sat
elevatis, glabris, nitidiusculis notato; elytris basi paulo dilutiori-
bus, rugoso-punctatis, singulatim 3-costatis, costa prima pone
medium evanescente; pectore flavo, abdomine nigro, segmentis
ventralibus 5 et 6 albido-cereis ; pedibus pallide fuscis.
Long. 5 mill.
Voisin de JL. obscurus, Ern. Oliv. (Ann. Soc. ent. Fr.
1895, p. 146), dont il différe surtout par la premiére cdte
élytrale abrégée postérieurement.
Je lui conserve le nom inédit sous lequel l’avait désigné
Westwood.
(73. Dec. 28, 1829. Paré. This specimen bears a label
in the handwriting of Professor Westwood, “ ptiliniformis,
Westw., sp. nov.”
74, ‘75, 76. Jan. 11,1830,8 p.m. Pardé (3 examples) ; two
of these bear the number “ 1454,” a reference number of
which the meaning wascontained in an ‘‘ 8¥° (long) red-coloured
volume ”’ which did not reach Oxford. ‘This red vol. has
not been found, J. O. W.” is appended in pencil by Prof.
Westwood to Burchell’s allusion to it. The last entry in the
“ Brazilian notes” deals with the number 1345, for March
18th, 1829; so that the missing volume contains Burchell’s
recorded observations between this date and Feb. 10th, 1830,
from South Africa and Brazil. 99
the day he sailed from Pardé. The localities are fortunately
preserved in the “ Index.”
(7. Jan. 13, 1830, 8 p.m. “1454.” Pard,
@8. Jan. 24, 1830. 1454." Pard.]
Lucioua, Cast.
79-82. Sp.?, 4 g.—Afrique australe. LZ. caffre, Bohem.,
similis, sed major, pronoto dense reticulato-punctato,
medio longitudinaliter late nigro-fasciato.
[Three specimens bear Burchell’s nos. 89 [80], 90 [81],
91 [82], and were considered by Burchell to be the same as
no. 88, viz. no. 66 of the present paper. They were captured
with no. 88 at 7.30 P.M. on Oct. 6, 1814, at Nowsakamma
River. The possibility of the accidental transposition of
labels must, however, be bornein mind. The fourth specimen
bears the no. 93 [79], and was captured at 8 P.M. Sept. 2 and
26, 1814, at Sylvan Station. “ Vespere ad lucernam volabat.
Elytra antenne oculi et pedes nigra. Relique partes
pallide flave. 1 Duplic.” Catalogus. The Banksian
Collation contains the note “93. Lamp. aff. Lamp. flabellico
in statura et forma, cui thorax fusco-niger.”’ ]
Puorturis, Le Conte.
83. mesta, Germ., 1 2? .—Brésil, Minas Geraés.
[Oct. 28, 1825. In the Forest on the West and on the
East side of 8. Joao de Népomucéna. ]
84, 85. fruticola, Mots., 2 ex.—Brésil, Rio de J.
(84. March 16, 1826. In the upper part of the valley of
Catombi, and along the road thence to Rio Comprido and
Matto Porcos.
85. April 9, 1826. “ Lampyris. About the middle of
twilight, these begin to fly in great numbers about meadows
and bushy places; they are not seen for more than about an
hour.” |
86, 87. éneola, Blanch., 2 ex.—Brésil.
[86. Dec. 9, 1826, 8 p.m. At Rio das Pedrds; in the
Forest, Cubatio.
87. March 2, 1829. Porto Real (Nacional). The speci-
mens are numbered 1334. ‘lhe following notes refer to
them :—
“1334, Lampyris. Probably tie same species as 1330
7
(
100 Mons. J. Bourgeois on Malacodermata
[see below]. It is common here, in certain nights or states
of the weather, and perhaps at least foretels fair weather for
that night. Tts light is at intervals, and only (as in all the
genus) when flying. When taken it emits and withdraws its
light much more rapidly; as [it] seems as if the effect of
breathing, whereas in flying the light and dark intervals are
both much longer (abt 5 seconds more or less). 2. 8. [29].”
Burchell had captured what he took to be the larva of
P. lineola on March 1, 1829, in his garden at Porto Real.
The following note refers to it. The specimen itself has not
been found.
©1330. Larva of (Lampyris?). Caught in the garden
crawling on the ground at night, and detected by means of a
small spot of light at the head; but on being touched it
instantly emitted a much stronger light from every part or
joint of the abdomen which previously was quite dark. The
light proceeded only from the underpart: the back was dark
at all times. Led. 20a
The sudden increase of light which follows disturbance
strongly supports A. R. Wallace’s interpretation of the
luminosity of glow-worms as aposematic. ]
88. Sp.?, 1 ex.—Brésil, Minas Geraés. Sat magna, elon-
gato-elliptica, prothorace flavo, elytris fusco-nigris, an-
guste (quadrante apicali excepto) albido-limbatis.
[Oct. 26, 1825. At Discoberto; near Jofio Pedro’s house.
“ Lampyris.” |
Cantharidide.
CHAULIOGNATHUS, Hentz.
89-91. fallax, Germ., var., 3 ex.—Brésil, Minas Geraés.
(89. Oct. 22, 1825. “ Ina Roca (about 4 miles 8.8. W. of
the house of Discoberto) on the road towards Nepomucena.
Lampyris.”
90. Oct. 39, 1825. (In the forest) on the N.E. side of the
arraial of Sio Jofio de Népomucéna.
91. Nov. 3-6, 1825. See no. 25, p. 94.]
99. Sp.?, 1 g.—Brésil, 8. Paulo. [Feb. 2, 1827.]
93. Sp.?, 1 ¢.—Brésil, Porto Real (Nacional).
[Jan. 11, 1829. ‘ Staphylinus. Caught on the ground
from South Africa and Brazil. 101
at the back door, probably where it was attracted by animal
substances.” ‘his label may have been accidentally trans-
posed. |
94. Sp.?, 1 ex.—Brésil, Porto Real. [Feb.8, 1829. Boracao. ]
95. Sp.?, 1 ex.—Brésil, Minas Geraés. [Nov. 3-6, 1820.
See no. 25, p. 9#.]
96. Sp. ?, 1 ex.—Brésil, Organ Mountains, [Feb. 18, 1826,
9 P.M |
CANTHARIS, L.
97, 98. viridescens, F., 2 ex.—Afr. australe.
Le Catalogue de Miinich indique par erreur viridesczns,
F., comme synonyme de smaragdula, F., espéce brésilienne
qui a avec Ja premiere une certaine analogie de coloration,
mais en est néanmoins bien distincte.
[ Both these specimens bear a V, of which the meaning is
as follows, in Burchell’s words :—“ Sent to me by Villet as
Cape Insects, and were received at Fulham during my absence
in Brazil’ (Catalogus). |
99. divitiata, F., Syst. Eleuth. i. 1801, p. 802, 1 ex.—Afr.
australe. (Omis au Catalogue de Miinich.)
[No. 95. Captured Dec. 27, 1813, between Bethelsdorp
and Uitenhage, Cape Colony, ‘in mimosa vtt [?].’’ Burchell
puts only Telephorus in the Catalogus. In the Olivier Collation
we find “95. Telephorus?? similis Lampyro vittate.” |
100. Sp.?, 1 ex.—Brésil, Minas Geraés. [Oct. 28, 1825.
See no. 83, p. 99.]
101, 102. Sp. ?, 2 ex.—Brésil.
(101. Feb. 12, 1826. Organ Mountains. By the River
Pacaqué.
102. Nov. 8, 1828, 10 p.m. Cérrego Raiz. Between
Chapdda and Porto Real (Nacional).]
Discopon, Gorh.
Biol. Centr.-Amer., Coleop. iii. 2, p. 78.
103, 104. cinctus, Cast., 2 ex.—Brésil, Minas Geraés.
f103. Oct. 23, 1825. Discoberto. “ Lampyris.”
104, Nov. 1, 1825. Near Nepomucena. |
102. On Malacodermata from South Africa and Brazil.
105. Sp.?—Brésil, Cubatio. [Foot of Sierra, Dec. 14,
1826, 9 P.M. |
106. Sp. ?—Brésil, Organ Mountains. [Feb. 12, 1826. By
the River Pacaqué.]
107. Sp. ?—Brésil [Minas Geraés. Oct. 16, 1825. At
Discoberto on 15th.]
108, 109. Sp.?, 2 ex.—Brésil [Organ Mountains. Feb. 12,
1826. River Pacaqué.]
DarPHRON, Gorh.
Biol. Centr.-Amer., Coleop, iii. 2, p. 66.
110. Sp.?—Brésil [Minas Geraés. Oct. 14, 1825. At
Parahiba on 12th. Discobertoon 15th. ‘ Lampyris.”
Melyridide.
HeEpysius, Er.
111. ? oculatus, Thunb., 1 9 .—Afr. austr.
[No. 96. ‘‘ Malachius.” The origin of the specimen is
given in the only other word in the Catalogus, viz. ‘ Bouch.”
‘This indicates *‘ From Mr. Bouchenroeder’s collection at
Cape Town (115 insects), of which perhaps some may not be
African at all: and it would therefore not be safe to admit
them without careful examination into my Cape Fauna,’’]
[The collection also contains two Lampyrid larve in
addition to 57 A :—
112. July 11, 1827. S. Paulo. The specimen bears the
number 1211, referring to the following note, which is
accompanied by a shght sketch:—“ 1211. Lampyris.
‘wo luminous spots on the same ring at the hinder part
of the abdomen. It crawls with its feet, but assists with
the tail by bending it under in the manner of some
caterpillars, and resting the point on the ground as a
fulcrum pushes on the body forwards. 11. Gleaiae
113. July 26. Pard. The larvais numbered 1402, referring
to a record in the lost note-book.]
On the Capside: in the British Museum. 1038
X1.—Lhynchotal Notes—XX. By W. L. Distant.
HETEROPTERA.
Fam. Capside. (Part I.)
THIS paper represents the first results of a revision of the
Capside contained in the British Museum, and the exami-
nation of Walker’s types. The arrangement is largely that
of the earlier propositions of Reuter, with some qualifications
which express my own views as to the classification of this
very difficult family ; and these will be more fully explained
in my second volume dealing with the Rhynchota of British
India, which is now passing through the press.
Division HERDONIARIA.
Allied to the Myrmecoraria, Reut. Cuneus always dis-
cernible ; head prominent, sometimes very large, always with
a distinct longitudinal impression between the eyes; anterior
constricted area of the pronotum somewhat broad and long,
but never broader, and generally narrower, than the poste-
rior area; second joint of the antenne either very strongly
or slightly apically incrassated ; scutellum sometimes spined.
The genus Herdonius, Stal, I take as typical of the Her-
doniaria, and also include the genera Zacinthus, Dist.,
Zosippus, Dist., Xenetus, Dist., and Minytus, Dist. Saturnio-
miris, Kirk., Systellonotus, Allodapus, and probably some
other described genera may also ultimately be included.
FULGENTIUS, gen. nov.
Body subelongate. Head moderately large, distinctly longi-
tudinally centrally incised; first joint of antenne very little
longer than head, second joint longest, somewhat thickened
towards apex, third shorter than second but longer than
fourth ; rostrum imperfectly seen in carded specimen ; pro-
notum moderately tumid, the lateral margins oblique, the
anterior margin distinctly carinate, and transversely im-
pressed before middle, anterior margin less than half the
width of posterior margin, the last a little sinuate before
scutellum, which is tumid ; corium, including cuneus, about
as long as abdomen; cuneus about as broad at base as long ;
membrane with a long basal cell; legs moderately long and
slender; tibize somewhat longly setose.
104 Mr. W. L. Distant on the Capside
Fulgentius mandarinus, sp. n.
Black; antenne, eyes, legs, and membrane piceous ;
anterior margin of pronotum, first joint of antenne (excluding
apex and base of third joint) and apices of femora ochraceous;
corium with a transverse fascia before middle and between
clavus and lateral margin, and about basal half of cuneus,
greyish white; body beneath black, imperfectly seen in
carded specimen, but apparently with a greyish spot near
posterior coxee ; body above very finely and obscurely pilose.
Long. 8 mm.
Hab. China ; Namoa Islands (J. J. Walker, Brit. Mus.).
NICHOMACHUS, gen. nov.
Moderately elongate. Head broad, including eyes much
wider than anterior margin of pronotum, narrowed and
moderately deflexed in front of the prominent and exserted
eyes, lateral margin sinuate, disk strongly longitudinally
sulcate; antenne with the first joint short, shorter than ante-
ocular portion of head, second and third joints longest and
subequal in length, fourth shorter but longer than first ;
rostrum reaching the posterior coxa; pronotum strongly
constricted at about one third from anterior margin, forming
a distinct narrow anterior lobe, posterior lobe tumid, about
twice as long and much broader than the anterior lobe ;
scutellum very strongly conically gibbous and longly though
sparingly pilose; corlum (excluding cuneus) a little shorter
than the abdomen, its lateral margins sinuate, broadest at
the area of the interior angle, cuneus longer than broad;
membrane thickly and finely reticulate, with a single, narrow,
short, lateral cell.
Allied to Systel/onotus, from which it differs by the broader
head, larger and exserted eyes, conically raised scutellum, &c.
But for the longitudinally impressed head might be located
in the Pilophoraria.
Nichomachus Sloggetti, sp. n.
Cinnamon-brown ; eyes, scutellum, base and apical margin
of corium, cuneus, disks of meso- and metasterna, and abdo-
men beneath black; an oblique transverse fascia in basal
black area of corium, a transverse fascia to clavus beyond
middle, and a basal fascia to cuneus white; antenne (ex-
cluding basal joint), posterior lobe of pronotum, and apices of
femora infuscated ; membrane shining brownish ochraceous ;
two transverse subbasal fascize to abdomen beneath pale
in the British Museum. 105
luteous ; head and pronotum finely granulate ; scutellum
smooth, shining, sparingly longly pilose; clavus, corium,
and cuneus finely and thickly punctate, shortly, obscurely,
rigidly pilose. ;
Long. 54 mm.
/fab, Cape Colony; Deelfontein (Col. Sloggett, Brit. Mus.).
Division MIRARIA.
Genus KIONEUS.
Evoneus, Dist. Biol. Centr.-Amer., Rhynch. i. p. 416 (1893).
Kioneus lineatus.
Miris lineata, Butl. Proc. Zool. Soc. 1877, p. 89.
Hab. Galapagos Islands,
Genus Miris.
Miris ruficeps, sp. n.
Very pale ochraceous ; first joint of antennz and posterior
femora and tibie thickly speckled with sanguineous ; lateral
margins of pronotum and a central line traversing pronotum
and scutellum pale greyish; first and second joints of
antenne strongly pilose, first joint moderately incrassate,
almost as Jong as head and pronotum together, second joint
about twice as long as first; tibiee thickly and rather longly
pilose.
Long. 9 mm.
Hab. Cape Colony: Grahamstown (Brit. Mus.) ; British
East Africa (Gregory, Brit. Mus.).
Genus CREONTIADES.’
Creontiades, Dist. Biol. Centr.-Amer., Rhynch, ii. p. 237 (1883).
Kangra, Wirk. Tr. Ent. Soc. 1902, p. 257.
Creontiades stramineus.
Capsus stramineus, Walk. Cat. Het. vi. p. 120 (1873).
Kangra Dudgeon, Kirk, Tr. Ent. Soc. 1902, p. 257.
Creontiades sinicus.
Capsus sinicus, Walk, Cat, Het. vi. p. 120 (1873).
Creontiades angulifer.
Capsus angulifer, Walk, Cat. Het. vi. p. 126 (1878),
106 Mr. W. L. Distant on the Capsida
Creontiades filicornis.
Capsus filicornis, Walk. Cat. Het. vi. p. 96. n. 161 (1878).
Megacelum filicornis, Uhler, Check-list N.-Am. Hem. p. 18.
Head centrally longitudinally sulcated.
Creontiades incertus.
Capsus incertus, Walk. Oat. Het. vi. p. 111. n. 260 (1873).
Resthenia incertus, Atkins. Cat. Capside, p. 58 (1890).
Genus PANTILIUS.
Pantilius australis.
Lopus australis, Walk. Cat. Het. vi. p. 57 (1873).
Head ochraceous, eyes fuscous; first joint of antenne
testaceous, second ochraceous, with its apical third black ;
pronotum pale greenish, its anterior area ochraceous, lateral
margins and posterior angles purplish red; scutellum pale
greenish, its basal margin and a central line ochraceous ;
clavus and corium mostly pale purplish red, apical area of
clavus and lateral margins of corium pale greenish ; cuneus
ochraceous, its margins purplish red; membrane brownish
ochraceous, the veins purplish red ; body beneath and legs
ochraceous; tibiz pale greenish ; apices of posterior femora,
bases and apices of posterior tibia and the tarsi purplish red,
apices of tarsi piceous ; scutellum finely transversely striate,
excepting on the basal margin and central linear fascia ;
corium a little widened from base and attenuated posteriorly ;
bases of apical margin of corium carinate.
Long. 10 mm.
Hab. New South Wales: Tasmania ; Hobart (J. J. Walker,
Brit. Mus.).
Genus ZANESSA.
Zanessa pictulifer.
Capsus pictulifer, Walk. Cat. Het. vi. p. 126 (1873).
Genus KOSMIOMIRIS.
Kosmiomirts lucidus.
Capsus lucidus, Walk. Cat. Het. vi. p. 124 (1878).
Kosmiomiris rubrooynatus, Kirk. Tr, Ent, Soc, 1902, p, 253.
in the British Museum. 107
Note.—In this division Miraria and near the genus Pan-
tilius I place Peas Reuteri, Dist. (Biol. Centr.-Am., Rhyn.
i, p. 428, tab. xxxvil. fig. 5),—head distinctly sulcated ; and
for the same reason Jacchinus tabascoensis, Dist. (loc. cit.
p- 430, tab. xxxvii. fig. 10).
Division CYLAPARIA.
Valdasaria, Dist. Biol. Centr.-Amer., Rhynch. i. p. 242 (1883).
Monalonionaria, Reut. Ann. Soc. Ent. Fr. 1xi. p. 598 (1892).
Eucerocoraria, Kirk. J. Bomb. Nat. Hist. Soc. 1902, p. 294.
Cylaparia, Kirk, Wien. ent. Zeit. xxii. p. 13 (1903).
The name of this division was originally founded on that
of the neotropical genus Valdasus, Stal; this having since
been proved to be but a synonym of Cylapus, Say, it is
necessary to alter the divisional name as above.
ARGENIS, gen. nov.
Head broad, not horizontally produced in front of eyes,
which touch but exceed the width of the anterior margin of
the pronotum, distinctly longitudinally centrally impressed,
or very finely sulcate ; antenne with the first joint longer
than head, but shorter than pronotum, second joint almost
twice as long as first, third joint about one third shorter than
second; eyes large, globose; pronotum coarsely punctate,
transversely constricted before middle, posterior lobe tumid,
centrally very obscurely carinate, posterior angles subpro-
minent and a little tuberculous; scutellum triangular, the
apex somewhat acute; corium long, cuneus passing apex
of abdomen; membrane somewhat small; body beneath
obscurely seen, owing to typical specimen being carded.
Argenis incisuratus.
Capsus incisuratus, Walk, Cat. Het. vi. p. 121. n. 282 (1878).
ITab. Ceylon.
Walker’s very inadequate description of this species con-
tains the erroneous statement :—‘ Prothorax with no trans-
verse furrow.”
Genus SYSINAS.
Sysinas tibialis.
Capsus tibialis, Walk. Cat. Het. vi. p. 109. n, 245 (1873).
Resthenia tibialis, Atkins. Cat. Capside, p, 61 (1890).
108 Mr. W. L. Distant on the Capsidee
Genus HELOPELTIS.
Hlelopeltis clavifer.
Dulichius ? clawfer, Walk. Cat. Het. iv. p. 170. n. 2 (1871).
Helopeltis braconiformis, Walk. loc, cit. vi. p. 165 (1873) ; Waterh. Tr,
Ent. Soc. 1886, p. 459, pl. xi. fig. 4,
?
Division
Genus DISPHINCTUS.
Disphinctus fasciatus.
Capsus fasciatus, Walk. Cat. Het. vi. p. 122. n. 284 (1873).
Disphinctus anadyomene, Kirk. Trans. Ent. Soc. 1902, p. 264.
Disphinctus politus.
Monalonion politum, Walk. Cat. Het. vi. p. 163. n. 7 (1878).
Disphinctus formosus, Kirk. Journ. Bomb. Nat. Hist. Soc. xiv. p. 295,
pl. A. fig. 10 (1902).
Genus HYALOPEPLUS.
fHyalopeplus vitripennis.
Capsus vitripennis, Stal, Freg. Fug. Resa, Ins. p. 255 (1859),
ITyalopeplus vitripennis, Stal, Gifv. Vet.-Ak. Forh. 1870, p. 670,
Capsus lineifer, Walk. Cat. Het. vi. p. 122. n. 285 (1873).
Hyalopeplus lineifer, Kirk. Tr. Ent. Soe. 1902, p. 18.
Division LOPARIA.
Genus RESTHENIA.
Resthenia incisus.
Capsus incisus, Walk. Cat, Het. vi. p. 92. n. 151 (1873).
Resthenta jamaicensis.
Capsus jamaicensis, Walk. Cat. Het. vi. p. 101. n. 189 (1878).
Heterocoris jamaicensis, Atkins. Cat. Capsidee, p. 42 (1890).
Genus LOPIDEA.
Lopidea floridana.
Capsus floridanus, Walk. Cat. Het. vi. p. 97. n. 163 (1878).
Lopidea marginata, Uhler, Proc. Calif. Ac. iv. p. 249 (1894).
Walker’s description is faulty. ‘The first joint of the
antenne is not “ red,” as described, but inclining to fuscous
brown; the ochraceous lateral margin to the corium is also
omitted in the diagnosis.
in the British Museum, 109
Genus LOMATOPLEURA.
Lomatoplzura coceineus.
Capsus coceineus, Walk. Cat. Het. vi. p. 93. n. 152 (1873).
Lomatopleura hesperus, Kirk. Trans. Ent. Soc. 1902, p. 252, pl. v. fig. 1.
? Lomatopleura cesar, Reut. (fy. Vet.-Ak. Forh, 1875, no. 9, p. 67.
Division PH YTOCORARIA.,
CAPELLANUS, gen. nov.
Elongate ; head subtriangular, moderately produced; an-
tennee with the basal joint short, about as long as head,
second joint three times as long as first, third shorter than
second ; pronotum short, truncate at base; scutellum sub-
triangular ; corium long and with cuneus about reaching apex
of abdomen ; posterior femora incrassated ; cuneus longer than
broad.
Allied to Phytocoris.
Capellanus sparsus.
Lygus sparsus, Dist. Biol, Centr.-Amer., Rhyn, i. p, 484, tab. xxxvii.
tig. 19 (1893).
Hab. Guatemala (type, Brit. Mus.).
Genus PARACALOCORIS.
Paracalocoris sobrius.
Capsus sobrius, Walk. Cat. Het. vi. p. 115. n. 264 (1878).
Very pale ochraceous; two large obconical spots at the
base of pronotum and the corium purplish brown; lateral
margins of pronotum and corium, two small central spots on
anterior disk of pronotum, and a rounded spot on corium near
inner base of cuneus black; membrane pale fuliginous,
cellular marginal veins purplish red; first joint of antenne
purplish brown, second and third joints black, base of third
luteous.
Paracalocoris leprosus.
Capsus leprosus, Walk. Cat. Het. vi. p. 111. n. 253 (1878).
Paracalocoris sericeus.
Capsus sericeus, Walk. Cat. Het. vi. p. 117. n. 272 (1878).
Pronotum anteriorly thickly cinereously tomentose, con-
taining two central piceous spots.
110 Mr. W. L. Distant on the Capside
Paracalocorts capensis, sp. n.
Somewhat pale ochraceous; corium pale castaneous, its
lateral margin ochraceous; cuneus ochraceous, its apex and
basal and inner margins castaneous; membrane subhyaline,
slightly tinged with pale fuliginous ; body beneath, rostrum,
and legs pale ochraceous; eyes, lateral margins of pronotal
collar, two small rounded discal spots to pronotum, a lateral
spot to mesosternum, and the apex of rostrum black ; basal
joint of antenn purplish red, second joint ochraceous, its
base black and its apical area purplish red (remaining joints
mutilated) ; body above strongly greyishly pilose; basal joint
of antennee finely thickly pilose.
Long. 7 mm.
Hab. Cape of Good Hope (Brit. Mus.).
Genus NEUROCOLPUS.
Neurocolpus nubilus.
Capsus nubilus, Say, Hem. New Harm. Ind. p. 22. n. 10 (1881).
Capsus hirsutulus, Walk. Cat. Het. vi. p. 95. n. 158 (1873).
Neurocolpus nubilus, Kirk. (part.) Tr. Ent. Soc. 1902, p. 252, nec
mericanus, Dist.
Genus CALOCORIS.
Calocoris norvegicus.
Cimex norvegicus, Gmel. Syst. Nat. iv. p. 2176 (1788).
Capsus contiguus, Walk. Cat. Het. vi. p. 95. n. 159 (1878).
Capsus stramineus, Walk. Cat. Het. vi. p. 96. n. 160 (1873).
Calocorts laticinctus.
Capsus laticinctus, Walk, Cat. Het. vi. p. 127. n. 308 (1873).
Capsus ustulatus, Walk. loc. cit. p. 128. n. 309,
Ia the Phytocoraria I now place the Neotropical genus
Calocorisca.
Division CAPSARIA.
xenus LYa@us.
Lygus australis, nom. n.
Capsus inotatus, Walk. Cat. Het. vi. p. 116. n. 269 (1873), nom.
preeoce. Reuter (1871).
Lygus suffusus.
Capsus suffusus, Walk. Cat. Het. vi. p. 117, n. 270 (1873).
in the British Museum. 110
Lygus ethiops, nom. n.
Capsus limbatus, Walk. Cat. Het. vi. p. 117. n. 271 (1873), nom.
preoce. Fallén (1829).
Lygus pallidulus.
Capsus pallidulus, Walk. Cat. Het. vi. p. 116. n. 267 (1873).
A single specimen in very bad condition constitutes thie
type of this species.
Lygus illepidus.
Capsus illepidus, Walk. Cat. Het. vi. p. 115. n. 265 (1873).
Lygus? conspersus.
Capsus conspersus, Walk. Cat. Het. vi. p. 116. n. 268 (1873).
The type is in bad condition and without antenne.
Lygus maoricus.
Leptomerocoris maoricus, Walk. Cat. Het. vi. p. 146. n. 110 (1873).
Anterior area of pronotum pale ochraceous, sometimes with
two dark spots.
Genus PacILOScYTUS.
Peeciloscytus solitus.
Capsus solitus, Walk. Cat. Het. vi. p. 116. n. 266 (1873).
Type in very bad condition.
Genus CAMPTOBROCHIS.
Camptobrochis strigulatus.
Capsus strigulatus, Walk. Cat. Het. vi. p. 94. n. 155 (1878).
Genus Pa@cILOCAPSUS.
Pecilocapsus marginatus.
Capsus marginatus, Walk. Cat. Het. vi. p. 96. n. 162 (1878).
Pecilocapsus limbatellus.
Capsus limbatellus, Walk. Cat. Het. vi. p. 93. n. 153 (1878).
Peeilocapsus (Metriorrhynchus) afinis, Reut. Gify, Vet-Ak. Forh.
1875, no, 9, p. 74.
112 Mr. W. L. Distant on the Capsides
Genus DERZXOCORIS.
Dereocoris patulus. |
Capsus patulus, Walk. Cat. Het. vi. p. 120. n. 279 (1878).
Genus Liocorts.
Liocoris partitus.
Capsus partitus, Walk. Cat. Het. vi. p. 119. n. 276 (1878).
Genus BOTHRIOMIRIS.
Bothriomiris simulans.
Capsus simulans, Walk. Cat. Het. vi. p, 125. n. 295 (1878).
Bothriomiris marmoratus, Kirk. Ty. Ent. Soc. 1902, p. 271, pl. v. fig. 9,
pl. vi. fig. 16.
Division BRYOCORARIA.
Genus PHYSETONOTUS.
In the ‘ Biologia Centrali-Americana’ (Rhynchota, vol. i.
p. 285) I followed Stal in placing his Hecritotarsus pallidi-
rostris in the genus he had himself founded. I, however,
placed it in a distinct section of the genus—“b. Body ovate.
Pronotum prominently gibbous.” Subsequently Dr. Reuter
(Ann. Soc. Ent. Fr. 1xi. p. 894, 1892) has proposed the genus
Physetonotus for the reception of these species, making
P. atratus, Dist. (Ecerttotarsus), the type. The following
species must also be included :—
Liccritotarsus pallidirostris, Stal; EH. tncurvus, Dist. ;
HE. gibbus, Dist.; E. porrectus, Dist.; H. impavidus, Dist. ;
Ei. perobscurus, Dist.; E. tenebrosus, Dist.; EH. nocturnus,
Dist.; L. marginatus, Dist.; and E. procurvens, Dist.
ARASPUS, gen. nov.
Ovate, posteriorly widened. Head deflected from in front of
eyes, which are large, projecting beyond but not touching
anterior margin of pronotum. Antenne with the first joint
slightly longer than head, a little thickened towards apex ;
second joint considerably longer than first, very prominently
incrassate and pilose on its apical half; third joint slender ;
remainder mutilated. Rostrum apparently reaching the inter-
mediate coxe (the type a carded specimen) ; pronotum with
the basal margin rather more than twice the width of anterior
margin, basal margin truncate, becoming oblique towards
posterior angles ; scutellum tumid, basally foveate ; corium
in the British Museum. 113
convexly rounded posteriorly; cuneus a little longer than
broad; legs of moderate length, posterior femora thickened.
Araspus partilus.
Lopus partilus, Walk. Cat. Het. vi. p. 56. n, 27 (1878).
Hab. New Guinea (Brit. Mus.).
MERTILA, gen. nov.
Elongately oval. Head rather long and depressed in front
of insertion of antenne, of which the first joint is shorter than
head and attenuated at base; second joint much longer than
first, it and the remaining joints pilose. Rostrum not quite
reaching the intermediate coxe. Pronotum with an anterior
collar, which has its anterior and posterior margins carinate ;
subimpressed or distinctly constricted before middle, the
depression including two transverse callosities; posterior
area a little tumid; posterior margin about twice the breadth
of anterior margin, sometimes as long as broad. Scutellum
small, subtriangular, callous, foveate at base; hemelytra
much longer than abdomen; membrane with a single trian-
gular cell; legs moderately short and slender.
Mertila malayensis, sp. n.
Orange-red ; apex of firstand the whole of the second joint
of antenna, eyes, apex of rostrum, corium (excluding basal
area), cuneus, membrane, extreme apices of femora, tibia,
tarsi, and sometimes abdomen beneath, indigo-black ; head
with a distinct central ridge and a broad foveation on inner
side of eyes; pronotum a little hollowed between the anterior
callosities ; upper surface very finely and obscurely pilose ;
tibie finely setose.
Long. 5-6 mm.
Hab. Singapore (17. N. Ridley, Brit. Mus.).
Mertila ternatensis, sp. n.
In colour resembling CO. malayenszs, but with the first and
second joints of the antenne entirely indigo-black and the
legs entirely orange-red; body much more elongate; pro-
notum nearly as long as broad, very distinctly constricted
before middle, the lateral margins of the anterior lobe con-
vexly produced; corium distinctly coarsely punctate, the
suture behind claval apex divided and forming an oblong
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 8
114 Prof. N. Yakovleff on the Characteristic of
foveation ; apical half of membrane bronzy brown; abdomen
beneath orange-red.
Long. 6 mm.
Hab. Ternate (J. J. Walker, Brit. Mus.).
Division ?
SABELLICUS, gen. nov.
Resembling Dercocoris, from which it differs principally by
the structure of the antenne. [ead elongately depressed in
front of insertion of antenne, of which the first joint is as
long or a little longer than the head, prominently incrassated,
and sometimes compressed from immediately beyond base,
somewhat longly marginally pilose, with a distinct spur on
outer side of apex; second joint much longer than first, slender
at base and regularly and moderately incrassated towards
apex ; remaining joints mutilated in type. _ Kyes large, almost
touching anterior margin of pronotum. Pronotum with the
basal margin about twice as broad as anterior margin, with a
distinct pronotal collar, and with the posterior angles sub-
tuberculous ; rostrum reaching the intermediate coxee ; cuneus
slightly longer than broad, the fracture profound ; anterior
legs robust, the tibiz moderately incrassate; intermediate
and posterior legs mutilated in type.
Sabellicus apicifer.
Capsus apicifer, Walk. Cat. Het. vi. p. 124, n. 298 (1873),
Hab. Celebes: Makian (Brit. Mus.).
‘Type in bad condition.
Sabellicus sordidus.
Lopus sordidus, Walk. Cat. Het. vi. p. 57. n. 29 (18738).
Leptomerocoris antennatus, Walk. loc. cit. p. 145. n. 109.
XIL—A Contribution to the Characteristic of Corals of the
Group Rugosa. By Prof. N. YAKOVLEFF.
WHILE engaged in investigating the Upper Paleozoic coral
Lophophyllum proliferum*, regarding which there have lately
* N. Yakovleff, “Fauna of the upper Portion of the Paleozoic
Deposits of the Donetz Basin,” Transactions of the Geological Committee,
new series, no. 12 (1903).
Corals of the Group Rugosa. 115
been published the interesting researches of Duerden *, I had,
in the first place, the opportunity of verifying the results of
Duerden’s labours, which are of certain importance in estab-
lishing the general characteristics of the Rugosa, and,
secondly, of adding a few data to these characteristics.
As is known, the distinguishing feature of the Rugosa is
considered to be the fact that they possess four primary septa,
of which two—the main septum and the counter septum—are
in the plane of symmetry of the coral, and the other two—
the alar septa—on either side of the plane. Besides, in
the quadrants between the primary septa the secondary septa
are arranged pinnately as regards the main septum in the
quadrants which adjoin it, and parallel with regard to the
counter septum in the counter quadrants.
The septa belong to two cycles, of which one consists of
large and the other of small septa. It is interesting to
observe the way in which the septa are developed in the coral.
As proved by Duerden, the septa of one cycle—the small
ones—appear comparatively late, simultaneously, and at a
certain height. As to the septa of the other eycle—the prin-
cipal ones—their mode of development has led Duerden to
approximate the Rugosa to the group of now living Actinia—
Zoantheee,—their development precluding the possibility of
approximating them, as is generally done, to the Hexacoralla,
which form a skeleton, and of regarding the former as the
progenitors of the latter.
The section (fig. A, p. 116) nearest to the pointed end of
the coral is 2:1 mm. in diameter, and represents twelve septa,
of which (according to Duerden) are to be regarded as primary
not four, as usually accepted for the Rugosa, but six septa,
which are marked in the figure by the cipher 1. Four of them
are: the main septum I (H), the counter septum I (G), and
the alar septa I (S)—the two remaining septa I being situated
next to the counter septum, and forming with it interseptal
chambers in which (and exclusively in them) no new septa
of the same cycle are developed.
Comparing figures A and B, we notice that the difference
between them is but slight, consisting chiefly in this, that the
main septum in the Russian specimen is situated on the convex
side of the coral, and in the American on the concave side, The
same coral in both specimens is bent in an opposite direction.
The observed relationship between the degree of development
of the main septum and the counter septum in a radial direction
* J, E. Duerden, “On the Relationships of the Rugosa to the living
Zoanthew,” Ann, & Mag. Nat. Hist., May 1902, p. 381. i
g*
116 On Corals of the Group Rugosa.
is in all probability owing to the direction of the bend; the
primary septum on the concave side (in the Russian specimens
the counter septum and in the American specimens the main
septum) is short and the primary septum on the convex side is
long (figs. Aand B). It seems to me that, with regard both to
A B
G4)
A and B, the corresponding sections of the Russian and American
specimens (the latter after Duerden, modified as regards the main
septum and the counter septum, see below, at end) of Liopho-
phyllum proliferum ; the portions of the sections turned upwards
lie on the convex side of the coral. The primary interseptal
chambers in which no new septa are formed are striated. I,
I (H), 1 (G), I (5), the primary septa; 1, 2, the later principal
septa.
the main septum and the counter septum, the fact may be
easily explained by supposing that the bend of the coral on the
concave side causes a contraction, affording less space for the
development of the septa than on the convex side; the former
is characterized by contraction, the latter by distention.
‘This assumption is strengthened by another peculiarity of
the coral, viz. that of the four primary interseptal chambers,
in which the successive principal septa are generally deve-
loped, the two situated nearest to the convex side develop the
septa more rapidly (in greater number). ‘These chambers
are not the same in the Russian and American specimens: in
the former (fig. A) they are contiguous with the main septum,
in the latter they are separated from it as well as from the
counter septum by other primary chambers.
In examining the two specimens (figs. A and B) we must
also notice that in two of the four primary chambers no nevw
septa are formed—invariably in those primary chambers which
On the Distribution of Marine Animals. LAF
adjoin the counter septum,—either on the convex or concave
side, and whether it be long or short.
We thus arrive at a more complete defiaction of the primary
counter septum: it is that (L) cn relation to which the con-
tuquous septa are arranged tn a parallel direction, and (2) which
has adjoining primary interseptal chambers, containing no
secondary principal septa.
Duerden is not correct in stating that the main septum and
the counter septum lie respectively on the convex and on the
coneave side of the coral independently of the arrangement
of the contiguous septa. This very arrangement has been
regarded by paleontologists as characteristic of the primary
septa, and, as will be seen from the above, it is more
permanent than has hitherto been known.
XILT.—On the Distribution of Marine Animals *.,
By Prof. M‘Intosu, M.D., LL.D., F.R.S., &e.
THE distribution of land-animals is a subject which has
always been fraught with deep interest to naturalists—more
especially as certain regions are characterized by the forms’
inhabiting them. Thus it would be anomalous to find, for
instance, a marsupial in Africa, an armadillo or a sloth
(Bradypus) in Asia, or a stag in Australia. ‘The chief
barriers, moreover, to the general distribution of such forms
have been mountain-chains, deep tracts of the sea, barren
regious such as the great deserts, and the vicissitudes of
temperature. Yet certain aerial forms, such as the bats, are
more or less cosmopolitan, and the shrews, the pigs, and the
mice are almost so. In weighing the statement, however,
that the distribution of certain of these forms, such as the
pigs, has been extended by their swimming powers across
arms of the sea, it has to be borne in mind that even marine
animals do not always avail themselves of the lines of migra-
tion at their disposal.
As three fourths of the surface of the globe are composed of
water—for the most part continuous throughout—a vast field
exists for the distribution, under natural conditions, of its
inhabitants, from mammals to Protozoa. Pelagic types may
thus range from pole to pole and from the eastern shore of
the Isthmus of Panama round the world to the western.
* Notes of an Introductory Lecture, 16th October, 1903,
118 Prof. M‘Intosh on the
Attempts have been made to divide this vast area into
regions characterized by special features. For instance,
Prof. Forchhammer, of the Chair of Mineralogy in the
University of Copenhagen, in 1862 described no less than
eleven regions distinguished by the mean quantity of solid
matter in the water, the tropical regions containing the
greatest amounf.
For facility in describing the collections made by the
‘Challenger,’ seven regions of the ocean were made, viz. the
North Atlantic, the South Atlantic, the South Indian or
Kerguelen, the Australian, the Philippine or Japanese, the
North Pacific, and the South Pacific. Taking the seals,
sirenians, and whales as a basis, Dr. Sclater has compara-
tively recently (1899) made six regions, viz. North Atlantic,
mid-Atlantic, Indian, North Pacific, mid-Pacific, and Antarctic.
This classification is useful in emphasizing, amongst other
things, the fact that even with the continuous medium, which
permits migration in various directions, certain forms cling
to special areas. It lacks, however, corroboration from the
other divisions of marine animals, and embraces so wide a
subject that further consideration of all the facts is desirable.
In passing therefore the distribution of the chief groups of
marine forms under review, the first amongst the marine
mammals are the sea-otters (Hnhydris), which often swim
10 to 15 miles from land, and are confined to the area of the
North Pacitic. ‘They do not appear to be spreading, but, as
Beddard says, persecution by man has made them more
purely oceanic.
The eared seals are chiefly confined to the south Polar
ocean. Three species are found all over the North Pacific
area, Whilst two frequent the west coast of South America
(Sclater). ‘The walruses are Arctic, the sane species probably
occurring in the North Atlantic and the North Pacific, though
the latter by some is considered distinct. The seals (Phocide)
are most numerous In the Arctic and Antarctic seas and in
certain intermediate areas. In the North Pacific three out
of four seals are identical with those in the North Atlantic.
The true seals of the Antarctic Ocean are all distinct from
those of the Arctic seas (Sclater). Thus the seals, as a whole,
do not support the theory of the bipolarity of marine forms.
The peculiar range of the living Sirenians and their struc-
tural features would seem to point to an inaptitude for
migration, especially in the case of the manatees, yet the
dugong and Steller’s sea-cow might have passed from islet to
coast-line and spread over a greater area, unless temperature
or other circumstance (e. g. food) had proved inimical.
Distribution of Marine Animals, 119
It might be supposed, again, that species so active and so
powerful as the whales would range over the whole ocean,
from the Arctic to the Antarctic seas. Yet in viewing their
distribution it appears that, with the whole stretch of the
ocean at their command, they, with the exception of the
dolphins, frequent special areas. Thus the right- or whalebone-
whales are confined to the temperate and cold regions of both
hemispheres. The Arctic right-whale haunts the neighbour-
hood of ice, under which it frequently takes refuge. Tempe-
rature may thus have an important bearing on its distribution ;
but, granting this, it has also to be remembered that nowhere
but in such waters could it find a pelagic fauna so rich in
large Clones and other Pteropods and of large Copepods
intermingled with Medusee, on which it delights to feed.
Moreover, nowhere could it, one of the most timorous
mammals, find such vast solitudes, where it can roam without
molestation. The same causes probably affect the distribution
of the southern right-whale, and it is at least known that its
active pursuit led to its rarity in Kuropean waters, for it is
less rigidly confined to the Antarctic seas than the northern
species to the Arctic. Another species of small size (Neo-
balena) is confined to the seas of Australia and New Zealand.
Food, environment, and temperature may have an important
bearing on limitation in this case.
Of the toothed whales the sperm-whales and the Ziphioids
have an extensive range, being, as Beddard says, “ equally
at home in the calm seas of the tropics and in the stormy
waters of the Antarctic ocean,’’ as well as in the North
Atlantic. ‘The former, as a rule, is an inhabitant of the
deeper waters far from land, probably because the cuttlefishes,
which form a favourite article of diet, are most plentiful there,
yet it also feeds on fishes, even, like the porbeagle shark,
stripping the fishermen’s lines, and occasionally swallowing a
shark or a seal. This varied dietary is consistent with its
wide range in the ocean.
In the family of the Dolphins, Beluga is for the most part
Arctic, only rarely being seen on European shores; but it
ascends rivers, e. g. the St. Lawrence, as Prof. Prince, the
Dominion Commissioner of Fisheries, tells me, for 150 miles,
apparently after salmon. ‘The narwhal frequents the same
oceanic region. ‘lhe common porpoise is Northern Atlantic
and Pacific; another occurs off South America and in the
Pacific ; whilst Neomerds is found in the seas of India, the
Cape, and Japan. ‘The dolphins frequent all the oceans, seas,
and great rivers of the world, and they are capable of adapting
120 Prof. M‘Intosh on the
themselves to every vicissitude of climate. Nor do their
layers of fat seem to present notable differences in the several
regions. As they are piscivorous, their food is obtained
without difficulty in every ocean and river. The killer (Orca)
is likewise cosmopolitan, its chief food consisting of seals and
porpoises. Globicephalus melas has also a wide range—from
the northern seas to the Cape and New Zealand—and Tursiops
is nearly as extensively distributed.
On the other hand, most of the species of Sotalia are
fluviatile, occurring in China and with Zntéa and Pontoporia
in the Amazons and other rivers of South America, whilst
ene species (a vegetable feeder) frequents the Cameroon
River.
With a distribution so complex, in an element which offers
no obstacle (except temperature, safe surroundings, and food)
to a cosmopolitan range for every species of marine cetacean,
the question as to the explanation of these diversities presents
itself. Why does Beluga not frequent European seas, or
Berardius of New Zealand stretch far northwards into the
Pacific? Beyond the answer that each finds in its special
area suitable environment and the food best fitted for it, no
answer is at present available. Hereditary tendencies, pecu-
liarities of stiucture, and habit are, perhaps, responsible for
the pertinacity with which the anomalous dolphins, like
Platanista, cling to fresh water, though it is true one genus
(Sotalia) is found equally in the Amazon and the sea. Nor
does the distribution of the whales throw much light on their
origin. So far as facts warrant, it would appear that the
toothed whales are the primary forms from which those with
whalebone have been evolved, but whether from a marine or
a freshwater form cannot yet be answered with certainty,
though the number of oceanic species shows that the sea at
least proved a congenial area. ‘he enormous lapse of time
necessary for the development of the various groups further
indicates that the ocean-basins are of great antiquity, though
they may not always have had the same conformation.
The distribution of certain birds (which pass most of their
time at sea), such as penguins, auks, grebes, divers, and
guillemots—all, with the exception of the first, possessing the
power of flight,—is limited to the colder areas; yet there is
no serious impediment to their ranging over a much larger
field except the difficulty of a secure breeding-place and the
question of temperature. Food is everywhere abundant. In
all probability it isthe safety and convenience of their
‘ rookeries ” which keep the penguins to the southern seas. °
Distribution of Marine Animals. tZE
A few Batrachians, Mr. Boulenger tells me, live in
brackish or salt water, such as Rana limnocharis, Bufo halo-
phila, and to a certain extent the European Bufo viridis and
Bufo calamita ; but as their eggs only develop in fresh water,
their opportunities for oceanic distribution are limited and
need not at present be further dealt with.
In addition to the semimarine [guanids—Amblyrhynchus,
which enters the sea (by diving) to feed on seaweeds, Tropi-
durus, and the various turtles,—marine reptiles are only found
amongst the snakes, if the estuarine crocodiles and Trionychoids,
which occasionally wander some miles seawards, are passed
by. As Mr. Boulenger* observes, “no better instance of
gradual modification from terrestrial into marine forms could
be found than in the snakes living at the present day, amongst
which are also to be found the only recent reptilian types
that, being viviparous, never leave the water.” These are
the Hydrophids or sea-snakes, the largest of which is about
12 feet long. They are, as described by the author just
mentioned, found in the Indian and western South Pacific
Oceans, ranging from the Persian Gulf to North Australia,
one species (ydrus bicolor) stretching throughout the Indian
and tropical Pacitic Oceans, the extreme points being the
Cape of Good Hope and Guayaquil.
As snakes are most abundant in tropical and subtropical
regions, it would appear that certain land-snakes in these
parts had gradually adapted themselves, probably in con-
nexion with food, to marine life—so much so that some are
never known to leave the water. Yet their distribution has
been limited, perhaps partly by temperature, though they
probably have extended considerably from their original
centre. It may be also that they are kept in check by the
large predatory forms, such as Hlasmobranchs and Cetaceans.
The marine fishes are, perhaps, more actively and charac-
teristically pelagic than any other group. As already shown,
the obstacles which oppose the distribution of Jand-animals
are absent—food and temperature chiefly requiring con-
sideration, though the abundance of the former in every sea
almost removes it from such a category. Another factor,
it is true, is the pelagic or demersal condition of the eggs,
since the latter habit might be supposed to have the effect of
making the proximity of the shores, or at least of the bottom,
a necessity at certain seasons. Yet one of the best known
and most widely distributed amongst pelagic fishes, the
herring, has demersal eggs.
* Nat. Science, vol. i. p. 45 (1892).
122 Prof. M‘Intosh on the
Mr. Wallace thinks that temperature and the depth of the
water are of primary importance in the distribution of the
marine fishes, for many species are adapted for shores and
shallows. Yet it is difficult to see how either acts; for
example, some shore-fishes, like the five-bearded rockling,
have pelagic eggs and still more actively pelagic young, so
that the question is complex. It must be admitted, however,
that many peculiar fishes frequent the great abysses (the
temperature of which does not vary much).
Is temperature sufficient to explain the varied distribution
of the vast variety of fishes? Does it make impassable
barriers, for instance, between the temperate and the tropical
and subtropical regions? Such can hardly be the rule in
every case, since, as Mr. Boulenger has pointed out*, the
grey mullet (J/ugil capito) ranges from Scandinavia to the
Cape, and is as much at home at the mouth of the Congo as
off the shores of Northern Europe. Yet some, such as the
cod, prefer the colder northern waters, and range from the
shores of Norway to those of North America; whilst others,
like Chetodon and the Sphyrenide, choose the warmer
waters of tropical and subtropical regions. ‘The variations
in temperature which a fish is capable of enduring are not,
perhaps, sufficiently known, but the northern plaice survives
in the warmer waters of Australia after a protracted journey
of thousands of miles. Prof. Prince ¢, moreover, in an inter-
esting article on “Adaptation in Fishes,” mentions that
Prof. Jordan found in the volcanic geyser area of the Yellow-
stone Park suckers and chubs in water of 85°-85° F., and
young trout in a temperature about 75° I’. It is long since
the eggs of the flounder were heated in a test-tube at St. An-
drews, and yet they survived and healthy larvae were hatched
from them.
Moreover, in roughly grouping the fishes under Dr, Sclater’s
six oceanic regions the families seem to be inextricably inter-
woven throughout, some occurring in every area or ranging
from the North Atlantic to the Indian Ocean, and thence to
the Pacific. A few features given by Mr. Wallace from
Dr. Giinther’s work are noteworthy. ‘Thus six families out
of about eighty are confined to the northern seas, and
amongst them are the suckers and the sturgeons. One family
(one genus and one species) is restricted to New Zealand
waters. Four inhabiting the depths of the ocean are only
found in the Atlantic, whilst thirteen families occur only in
* Poiss Ben. Congo, p. 355.
+ ‘The Ottawa Naturalist,’ vol. xiv. no. 1], p. 216.
Distribution of Marine Animals. 123
the Pacific. Two families (Lycodide and Gadide) inhabit
the Arctic and Antarctic seas only, though one species of the
latter (Gadidx) exists in the Indian Ocean. One extensive
genus (Diagramma, family Pristipomatide) is confined to
the Pacific, with the exception of a single species in the
Mediterranean. One family (Notacanthi) has representatives
in Greenland, the Mediterranean, and West Australia.
Lastly, the single representative of the family Lophotidee is
found only in Japan and the Mediterranean. Similar results
follow in considering the classification of Prof. Palacky, of
Prag *, Further and more minute investigation of the
several areas may reduce the number of these anomalies ; but
it is difficult to unravel the tangled web of the distribution of
fishes.
In glancing at the families most widely distributed it is
found that a considerable proportion of them have pelagic
eges, but others, such as the blennies, gobies, and pipe-fishes,
have demersal eggs, and the fishes themselves are not noted
for swift progression or nomad habits. From the fact that
some cosmopolitan forms, such as the Clupeoids, have both
pelagic and demersal eggs within the limits of the family,
this condition would not seem to be the chief factor asso-
ciated with their distribution. Some families have represen-
tatives on the shores of Britain, Chili, and Kamschatka,
whilst others frequent the open sea in all parts of the world.
Fishes, like the wrasses, which occur on the Huropean and
American shores and extend to Japan and New Zealand,
increase the complexity of the problem. ‘The facts of distri-
bution, indecd, may be associated with the origin of the fishes
from pre-existing forms, for the families could scarcely have
arisen as the result of variation since the land and water
had their present conformation. Again, the occurrence of
isolated species or genera at points widely distant from other
members of the family indicates, amongst other things, that
the production of species by variation is in some cases very
slow.
The comparatively recent origin of the Teleosteans has
made no noteworthy limitation in the distribution of the
families, in contrast with the much older group—Mollusca—
some of which are found in the Lower Silurian, though the
latter comprises forms less actively pelagic. Mr. Wallace
thinks fishes less cosmopolitan than mollusks, a feature he
attributes to the antiquity of the shell-fishes ; but it may be
due to other causes, such as food and temperature, which keep
* ‘Die Verbreitung der Fische ’ (Prag, 1895).
124 Prof. M‘Intosh on the
fishes to certain areas, for their powers of progression in a
continuous element are great.
The pelagic Tunicates, sueh as Salpa, Doliolum, Pyrosoma,
and the Appendicularians, are practically cosmopolitan,
ranging from the northern seas to the Antarctic. Thus
Prof. Herdman found Salpa runcinata fusiformis in water at
a temperature of 80° in the Gulf of Manaar, and the same
species occurs in the Antarctic seas. He has noticed that
some fixed forms, like Styela plicata, are also cosmopolitan or
range from the seas of Europe to those of Australia, He has
also drawn special attention to the large size and the abund-
ance of the Tunicates in the Antarctic regions. Simple
Ascidians, again, are perhaps more common in shallow than
in deep water, and few extend to the abyssal zone. Compound
forms appear to attain their greatest development in the south
temperate zone. Botryllidz are partial (if not confined)
the northern hemisphere. Distomidse are found in the
northern and southern hemispheres, whilst Polyclinidee are
southern (Herdman, ‘ Challenger’).
In the present state of our knowledge it can scarcely be
said that the sea can be mapped into regions by the distri-
bution of the Ascidians, or that there is any clue to their
origin from pre-existing forms by their occurrence in modern
seas. ‘l’emperature has little influence on the distribution of
the simple forms, for they range from nearly freezing-point
upwards (Herdman), though, as pointed out in a former
Introductory Lecture, they are more conspicuous on tlie
seaweeds of the west than the east coast of Scotland.
Out of fifty-eight families of marine mollusks forty-eight
are cosmopolitan, but the limitation of a whole family to an
area occurs very seldom. Tor example, while most of the
cones are tropical, Wallace points out that Pleurotoma is
cosmopolitan. In the same way the volutes are tropical, but
Mitra occurs in Greenland. ‘he cowries are also charac-
teristic of warm regions, yet one species is found in Britain
and one in Greenland. Of the cuttlefishes some, like the
argonaut and pearly nautilus, are characteristic ‘of, warm
seas, whilst the majority are cosmopolitan, their enormous
numbers in the great oceans being only occasionally in
evidence by their destruction of fishes on the lines, by the
oecurrence of their beaks in the stomachs of numerous fishes
(trom the cod and Lampris to sharks), and by their forming
the chief article of diet tor the sperm-whales.
That the mollusks have had ample time to spread them-
Distribution of Marine Animals. 125
selves over the great oceans is proved by their antiquity,
many, like both groups of truly pelagic forms (the Heteropods
and Pteropods), ranging back to the Silurian period.
Their complex distribution is not easily explained. Was
the Pleurotoma of Greenland evolved from the same stock as
the cones of the tropics, or did each arise from pre-existing
forms in the special areas? Why are the pearl- -oysters
(Aviculidze) tropical or subtropical, like the giant-clam
(Z'ridaena) ? Why should the conditions accompanying the
formation of pearls in the former be limited to special regions,
even though the presence of certain fishes be necessary ?
The marine Insecta are comparatively few, and it will
suffice to take the two genera described by Dr. Buchanan
White * from the collection of the ‘Challenger.’ Thus five
species of [Ha/obates occur in the Atlantic, but only one is
restricted to it. Six species are found in the Indian Ocean
west of long. 100° E., whilst (chiefly) in the West Pacific
eight species are met with, of which four are restricted to
that region. The metropolis of the genus appears to ba the
Indian Ocean and West Pacific, fon nine out of the eleven
known species occur there, and White thinks even originated
there, and that currents have carried them eastward. The
other genus ([/alobatodes) is represented only in the Indian
Ocean and the China Sea. The Halobatidz are therefore
chiefly inhabitants of the warmer seas, and though they have
co)
not spread over the whole ocean, they are widely distributed.
In the class Crustacea the distribution of marine forms is
remarkably wide, just as the number of some of the smaller
forms like the Copepods swarm in every sea, from pole to
pole. Thus a species of the Amphipod Podocerus extends,
Mr. Stebbing informs me, from the waters of New Zealand to
77° UV -N.«, and another from Tahiti to the Faroés. The
higher Crustacea are sensitive to temperature, as is evident
from the behaviour of such forms as the shore-crab in summer
and winter, and, as Mr. Stebbing observes, by the paucity of
species in Arctic, Antarctic, and very deep waters. Yet, as
this experienced author states, there are Amphipods and
Isopods which abound most and attain their greatest size in
Arctic waters. ‘The comparison of the Copepods (Calanz &c.)
from the feeding-grounds of the right-whale with those in
European waters is equally pronounced, the size of the Arctic
forms being much greater. Mr. Stebbing mentions that
oOo
every fresh expedition tends to show the intimate relationship
* ‘Challenger,’ vol, vii. pp. 77 & 78.
126 Prof. M‘Intosh on the
of the marine Crustaceans from north to south and east to
west. ‘* Land-crabs and river-crabs are chiefly confined to
warm climates, Again, very few crabs occur at either end of
the globe, but that does not prevent the discovery of many
erabs living in deep and therefore very cold water in the
intermediate zones. There i is, besides, a sort of zonal facies,
which an expert in each group would probably recognize.
There are circumpolar Amphipods, Isopods, and Sympods
(Cumacea), which one would regard with great suspicion if
it was said they had been collected at the tropics. But, never-
theless, the deep-water communication accounts for the closest
family connection between members of the Lithodide found
far north and far south.” (Stebbing.) The same author is of
opinion that in some cases there may be isolation and
restricted distribution, these seldom going beyond specific
distinction. Yet as regards the Crustacea it is difficult to
make regional areas of demarcation in the ocean. It would
also be difficult to say that any family of marine crustaceans
is exclusively tropical and another as exclusively Arctic, and
though certain forms are found in deep water (e.g. the Japanese
Thaumatocheles), yet representatives of the same family may
occur in shallow water.
In dealing with the families of the marine Polycheeta it
is also impracticable to map out the ocean in regions to
suit their distribution, for almost every family has repre-
sentatives in diverse regions; and although of some it may
be said that they are more prominent in tropical or sub-
tropical waters, yet other representatives range to the poles.
As examples of families usually considered characteristic
of the warmer parts of the sea are the Huphrosynide and
Amphinomide, yet examples of both occur in Norway and of
the former in Greenland ; indeed their range is almost
cosmopolitan. The Eunicide likewise are often conspicuous
in tropical and subtropical seas, yet the abundance and size
of some from the shores of Norway and from the North
Atlantic show the cosmopolitan distribution of the group.
With our present knowledge it can hardly be said of any
family that it is, on the one hand, a purely northern or a
purely southern, or, on the other hand, a purely temperate
or a purely tropical one. Some Annelids range trom Green-
land to Japan, from Norway to the Cape and New Zealand,
and many are cosmopolitan.
In considering how it has happened that the same form is
found in Greenland, Europe, and Japan, some, like Sir John
Murray, would suppose that such had been universally dis-
Distribution of Marine Animals. 127
tributed in the ocean at a former period, but that physical
changes had subsequently restricted the range. Others see
in this condition proof of the enormous powers of dispersion
at the disposal of marine organisms, and the origin, in the
several areas, from a pre-existing form.
Moreover, whatever may be the conditions (and Sir J.
Murray thinks the quantity of carbonate of lime secreted by
marine organisms is determined by the temperature of the
water and therefore chiefly chemical rather than physical) in
regard to coral-reefs, northern Annelids (e.g. Hiligrana
impleca and other Serpulide) have no difficulty in forming
considerable masses of calcareous tubes *. ‘Temperature
appears to have no appreciable influence on the abundance
and size of these calcareous tubes in cosmopolitan species.
Nor is there a distinction in regard to the calcareous secre-
tions of the Polyzoa and Echinoderms of the extreme north
from those in the tropical oceans.
The families of the Nemerteans have a range as wide as
that of any previous group, and the type of structure varies
little whether the form be arctic, tropical, or antarctic. Of
no special region of the ocean can it be said that its Nemer-
tean fauna is diagnostic, for with advancing knowledge
(largely due to the labours of Mr. R. C. Punnett) the dis-
tribution of the types is always extending. There is no
evidence, moreover, that the arctic and antarctic forms have
other relationships than those which spring from a cosmo-
politan distribution.
So far as can be ascertained, the families of the Echino-
derms correspond with those of other groups in regard to
distribution. Some range from the arctic to the antarctic
seas, and, as Mr. Bather observes, from the eastern shores
of America round the world to the western, the same
species thus occurring on the opposite shores of the Isthmus
of Panama. It has, however, to be remembered that a com-
munication existed between the respective sides up to a
recent period. Some, again, range to great depths as well as
have a wide distribution.
As in other groups, some forms suggest a northern area
and some.a tropical, but “on the whole it cannot be stated
that there are special regions of the ocean characterized by
special families of Echinoderms, though it is true that certain
types, like the Pentacrini and El lasipoda, occur in deep water.
* Murray thinks that those forms secreting a large quantity of car-
bonate of lime would be killed by the lowering of temperature at the
poles—like those with pelagic larvee,
128 Prof. M‘Intosh on the
Further, the slightly pelagic Ophiopteron of Amboyna, one
of the Moluccas, is not so widely distributed as some other
types devoid of such an apparatus for progression,
The distribution of the Ccelenterates, such as zoophytes,
jelly-fishes, sea-anemones, corals, and sea-fans, presents
special features, for some are more purely tropical, others
more characteristic of the colder areas, whilst not a few—like
Campanularia, Obelia, and Eudendrium—are cosmopolitan.
Thus the coral-reefs are tropical and subtropical, yet some
stony corals, such as Lophohelia and Caryophyllia, occur
in temperate seas. The jelly-fishes and sea-anemones are
cosmopolitan, though some, like Cestus, are characteristic of
the warmer seas. Alcyonarians range from tropical to cold
regions, those in the former, however, according to Prof.
5 . . . . .
Hickson, being distinguished by the abundance of their
coo}
spicules or by massive skeletal structures.
Sponges are often widely distributed, some forms being
common to the North Atlantic and the Cape, others to the
latter and Australia; whilst European types range to South
Africa and America.
The Foraminifera, Radiolarians, and other types of the
Protozoa (e. g. Nocttluca) have an extensive distribution,
the former ranging from the Arctic to the borders of the
Antarctic Ocean, and forming vast deposits in many areas,
The distribution of Woctiluca and the pelagic forms like
Ceratium is equally wide; nor is there any hard-and-fast
line separating the distribution of families or larger groups
from each other. .
In connexion with regional distribution in the ocean, it
has been supposed by some that the fauna of the deep water
(abyssal region) is peculiar, but many families found there
have representatives in shallower water aud even between
tide-marks. Thus amongst the deep-water fishes the Mure-
nidee include the eels socommon between tide-marks in the
Channel Islands and elsewhere. ‘The Clupeide comprise
the herring, sprat, and anchovy—widely distributed pelagic
fishes which come near the shore to spawn. ‘The Ophidiidee
are almost universally spread from Greenland, to New
Zealand, and the family includes the sand-eel of our shores.
In the same way the Pediculati, another family of deep-water
fishes, has a representative, viz. the frog-fish, in shallow
bays. A considerable number of Mollusca are also inhabi-
tants of the depths of the sea, but representatives of the
came families or even genera occur in shallow water; and
Distribution of Marine Animals. 129
so with the marine Polycheta and other Invertebrates
down to the Foraminifera—only arenaceous forms of the
latter are more abundant in abyssal regions, and it is said
that no Brachyurous crustacean has been met with below
1000 fathoms (Canon Norman).
Sir John Murray thinks that migration into the deep sea
took place from the mud-line (viz. about 100 fathoms), and
that there is little evidence, from the observations made in
the ‘Challenger,’ to show that the deep sea has been peopled
since the earliest geological times. The uncertainty on this
head, however, is apparent by the statement of Prof. James
Geikie that it was the absence of these abysses in early times
(Paleozoic) which enabled many forms to become cosmo-
politan. Murray, again, considers that the fauna of the deep
water is less ancient than that of many shores (Lingula and
Heliopora) and freshwaters (Ceratodus). In considering the
deep-water fauna, however, it is well to bear in mind the
difficulty of bringing the animals up for investigation.
A brief glance may now be taken at the bipolarity of
marine animals as promulgated by Pfeffer and Murray. The
latter, especially from his experiences in the ‘ Challenger’
expedition, has put forward a strong claim on this head.
He is of opinion that there area large number of identical
and closely allied species in the extra-tropical regions of the
northern and southern hemispheres, which, so far as known,
are not represented in the intervening tropics—even though
the climatic conditions as regards temperature are the same.
He thinks that the identical species now living towards both
poles, or their immediate ancestors, had a world-wide distri-
bution, which involves a nearly uniform temperature through-
out the whole body of the ocean (probably in Middle Meso-
zoic times), and that as the poles cooled these animals were
drawn towards the equator. As we go back to the Paleozoic
period, he affirms, the tropical zone of temperature slowly
widens. Murray further supports his theory by pointing
out that pelagic larve are absent in the cold waters of the
arctic and antarctic regions; yet this may have been acci-
dental, and due to the depth at which the tow-nets were
used. Certainly the Sponges, Ceelenterates (Zoophytes),
Kchinoderms, Annelids, and Molluses of these regions have
ciliated pelagic larvee. This bipolar theory has been opposed
by Ludwig for the Sea-Cucumbers, Ortmann for the Crus-
taceans, and D’Arcy Thompson generally, whilst many of the
appearances may be explained by the cosmopolitan distri-
bution of the various types.
In summing up, therefore, it would appear that the distri-
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 9
130 Mr. G. A. Boulenger on new
bution of marine animals has features which diverge from
those which characterize the distribution of land-animals—
according to the views now prevalent; and, further, that
the absence of impassable barriers does not, of necessity, lead
to a cosmopolitan habit in those which can avail themselves
of the opportunity. In the case of lJand-animals much
weight has been placed on this check to migration, so that
it is a prominent feature in the literature of the subject.
Further, the conditions in the ocean tend to the permanence
of the various types, which, with their wide distribution,
varied sites, and uniform medium, have much to favour them
in the struggle for existence. The vast or cosmopolitan
distribution of many forms is thus conspicuous.
Again, in the present state of knowledge, the division of
the ocean into regions characterized by special faunistic
features can with difficulty, to say the least, meet with
support from all the groups of marine animals.
This preliminary survey of the subject, moreover, is in-
teresting insofar as it discloses no serious obstacle to the
introduction of Kuropean food-fishes, shell-fishes, crabs, and
other forms to various parts of the world—especially those of
primary importance to man. If, for instance, the same or a
closely allied shell-fish or annelid can live and flourish equally
in the waters of Britain and those of the Cape, there is pro-
bably no insuperable barrier to the transference of a valuable
food-fish from the one tothe other. The recent transmission
of adult plaice from Scotland to Australia has already met
with success, and the same experiment may soon be carried
out at the Cape.
Though at present, broadly speaking, no definite plan of
distribution amongst the families of oceanic forms is dis-
cernible—very few families being monopolized by one region
to the exclusion of the others,—future investigators may
enable such a plan to be outlined ; yet the number of cosmo-
politan forms, and of others which range almost as widely,
will always give a tone to the picture of the sea in contrast
with that of the land.
X1V.—Deseriptions of new Frogs and Snakes from Yunnan.
By G. A. BouLencer, F.R.S.
In a recent number of these ‘Annals’ * I described a new
gecko, Gehyra yunnanensis, obtained at Yunnan Fu (altitude
* Vol, xii. 1905, p. 429.
Frogs and Snakes from Yunnan. 131
about 6000 feet) by Mr. John Graham, of the China Inland
Mission. The Natural History Museum has since received
from the same gentleman further collections made in the same
district, and among them I had the pleasure of finding
examples of two new frogs and five new snakes, of which
descriptions are here offered.
Rana pleuraden.
Vomerine teeth in two small oblique groups between the
choanze. Head moderate, as long as broad; snout obtusely
pointed, prominent, as long as the orbit; canthus rostralis
obtuse; loreal region oblique, concave; nostril equally
distant from the eye and from the end of the snout; inter-
orbital region narrower than the upper eyelid; tympanum
very distinct, two thirds to three fourths the diameter of the
eye. Fingers and toes rather slender, obtusely pointed ;
first finger extending beyond second; toes half-webbed ;
subarticular tubercles rather feeble ; a small oval inner meta-
tarsal tubercle, The tibio-tarsal articulation reaches between
the eye and the tip of the snout. Skin smooth or with small
warts; a moderately broad, very prominent, dorso-lateral
glandular fold; no other folds on the body. Olive-brown or
greyish above, spotted with black; a light vertebral streak
usually present ; a dark brown or blackish band on each side
of the head, passing through the eye and involving the
tympanum; awhitish streak along the upper lip; limbs with
more or less regular black cross-bars; sometimes a light line
along the inner side of the leg, continued to the outer toe;
hinder side of thighs marbled black and yellow; lower parts
white, throat sometimes brownish. Male with a vocal sac on
each side, forming loose folds on the throat, and a very large
flat gland on each side of the body, above and behind the
shoulder.
From snout to vent 63 mm.
Several specimens.
Callula verrucosa.
Snout rounded, not prominent, as long as the eye; inter-
orbital space as broad as the upper eyelid. Fingers slender,
with slightly swollen tips, first a little shorter than second ;
toes moderate, nearly half-webbed, the tips blunt, not swollen,
fifth considerably shorter than third; subarticular tubercles
well developed; metatarsal tubercles two, oval, compressed,
the inner very large. ‘The tibio-tarsal articulation reaches
the shoulder or between the shoulder and the eye. Upper
O*
132 Mr. G. A. Boulenger on new
parts with large smooth warts; a fold from the eye to the
shoulder. Dark greyish brown above, uniform or with six
longitudinal rows of small darker spots; lower parts uniform
dirty white.
From snout to vent 46 mm.
Three specimens, from the garden of the Mission station.
Closely allied to C. picta, Bibr.
Polyodontophis Grahami.
Rostral once and a half as broad as deep, just visible from
above ; suture between the internasals nearly as long as that
between the prefrontals ; frontal much longer than its
distance from the end of the snout, shorter than the parietals ;
loreal as long as deep; one preeocular; two postoculars, only
the upper in contact with the parietal ; temporals2+2; eight
upper labials, fourth and fifth entering the eye; four lower
labials in contact with the anterior chin-shields, which are
longer than the posterior. Scalesin 17 rows. Ventrals 185 ;
anal divided; subcaudals 83. Reddish brown above, with
three dark brown longitudinal lines, which become more and
more indistinct after the anterior fourth of the body ; head
dark brown, with a black streak on each side and a black bar
behind the parietals ; a white streak along the upper labials
and another behind the occipital bar; lower parts white, with
a black dot at the outer end of each shield; on the posterior
part of the body and on the tail these dots are confluent into
a black lateral line.
Total length 350 mm. ; tail 60.
A single specimen.
Intermediate between P. collaris, Gray, and P. sagittarius,
Cant.
Tropidonotus quadrilineatus.
Eye moderate. Rostral broader than deep, just visible
from above ; internasals broadly truncate anteriorly, a little
longer than broad, nearly as long as the prefrontals; frontal
once and a half as long as broad, as long as its distance from
the end of the snout, much shorter than the parietals ; loreal
as long as deep; one pre- and two postoculars; temporals
241; seven or eight upper labials, third and fourth or fourth
and fifth entering the eye; four lower labials in contact with
the anterior chin-shields, which are shorter than the posterior.
Scales in 19 rows, all keeled, the dorsals strongly. Ventrals
158; anal entire; subcaudals 51. Pale olive-brown above, with
two black vertebral lines, widening on the nape and occiput,
Frogs and Snakes from Yunnan. 133
and a broad black lateral band extending from the eye to the
end of the tail; black lines on the sutures between the upper
labial shields, which are white; lower parts bright yellow.
Total length 435 mm. ; tail 65.
A single male specimen.
This species appears to be allied to 7. Pealiz, W. Sclater,
from Assam,
Troptdonotus octolineatus.
Eye moderate. Rostral broader than deep, just visible
from above ; internasals broadly truncate anteriorly, as long
as broad, nearly as long as the prefrontals ; frontal once and
a half as long as broad, a little longer than its distance from
the end of the snout, much shorter than the parietals ; loreal
as long as deep; one pre-and two postoculars ; temporals
2+2; nine upper labials, fourth, fifth, and sixth entering
the eye; five lower labials in contact with the anterior chin-
shields, which are a little shorter than the posterior. Scales
in 19 rows, dorsals moderately keeled, laterals feebly, outer
row smooth. Ventrals 152; anal divided; subcaudals 58.
Pale greyish brown above, with two black longitudinal lines,
separated by five series of scales, these lines widening on the
nape and passing into the dark brown colour of the upper
surface of the head; a black lateral band extending from the
eye to the end of the tail; a black zigzag lateral line, formed
by the outer edges of the ventral shields; an interrupted
black line on each side of the belly, formed by a short streak
on each shield ; upper lip and lower parts yellow, the outer
ends of the ventral shields reddish; black spots or vertical
bars on the upper lip.
Total length 610 mm. ; tail 125.
A single female specimen.
This species is most nearly allied to 7. paratlelus, Blgr.
Tropidonotus pleurotenia.
Eye moderate. Rostral broader than deep, just visible
from above ; internasals narrowly truncate anteriorly, a little
longer than broad, a little shorter than the prefrontals ;
frontal once and a half as long as broad, longer than its
distance from the end of the snout, shorter than the parietals ;
loreal as long as deep; one pre- and three postoculars ;
temporals 2+153 eight upper labials, third, fourth, and fifth
entering the eye; five lower labials in contact with the ante-
rior chin-shields, which are as long as the posterior. Scales
in 19 rows, feebly keeled, two outer rows smooth. Ventrals
134 On new Frogs and Snakes from Yunnan.
148; anal divided; subcaudals 66. Yellowish olive above,
with two very indistinct darker streaks along the back ; a
blackish lateral band, extending from the eye to the end of
the tail; scales of outer row greyish, edged with black; upper
lip white, with some black on the sutures between the shields ;
lower parts uniform bright yellow.
Total length 350 mm. ; tail 85.
A single male specimen.
Allied to 7’. modestus, Gthr.
Pseudoxenodon sinensis.
Very closely allied to P. macrops, Blyth, with which
specimens from Sze Chuen have been confounded by Giinther
and by myself. Distinguished by having usually only seven
upper labials, third and fourth entering the eye, 19 or 20
scales on the middle of the body as well as on the neck, a
smaller number of ventrals, viz. 144 to 158 instead of 160 to
175, and a different coloration, the upper labial shields being
marked with black bars corresponding to the sutures, and the
quadrangular dark brown spots on the anterior part of the
belly being absent.
The numbers of ventral and caudal shields are as follows
in the specimens examined :—
©. Kia-ting-fu, Sze Chuen, 1070 f. (Pratt) ...... 158+ ?
: ” ” ” PPro. felts sl iolvele 158-+55
do. Son-pan-ouei, Sze Chuen, 10,000 f. (Styan) 144467
6. Munnan Fu, 6000 £AGrakam) s; xtc. hetente a oe 155 +67
” ” 99 Ai” HO COs ie ga, elie 0) ie ga ike ae jeige Re.ke 1544-62
In a fresh condition this snake is olive-green above, with
black and yellow or orange spots, the latter usually forming
a vertebral series, at least on the posterior part of the body ;
a blackish streak along each side of the nape, sometimes
united in a point on the occiput; an oblique black streak
from the eye to the angle of the mouth; frequently a light
cross-band between the eyes; loreal region and upper lip
bright yellow or orange, the labial shields with black lines
corresponding to the sutures between them ; belly yellow or
orange in front, uniform or speckled with blackish, greenish
or dark greyish olive behind, more or less profusely speckled
with black.
Total length 780 mm. ; tail 140.
On Fishes from the Cameroon Mountain. 135
XV.—On some Fishes from the Lakes of the Cameroon
Mountain. By Dr. Eryar Lonnpera, C.M.Z.S. &e.°
A FEW weeks ago I received from my friend Gunnar Linnell,
residing at Cape Debundscha, a small collection of fish which is
of considerable interest, having been obtained from the small
isolated lakes of volcanic origin on the Cameroon Mountain,
viz. Lake Barombi-ba-kotta and the Elephant Lake.
The natural conditions of the latter lake have been men-
tioned in my previous paper on fishes from the Cameroon
(Ann. & Mag. Nat. Hist. ser. 7, vol. xii., July 1903) and need
not be repeated. Concerning the Lake Barombi-ba-kotta,
the Swedish civil engineer P. Dusén gives the following
information * :—In the middle of the lake is a small islet of
basalt. On the western side there is a steep slope about
10 metres in height, but the surroundings are not very high
and crater-walls seem to be absent. Mr. Dusén is therefore
uncertain whether to regard this lake as a very old crater
or a “ Maar” formation. ‘The lake receives only a small
tributary, the rivulet Manatunge, at the mouth of which
basalt-rocks were seen ; but there is no watercourse leading
from the lake or draining it, so that it is thus fully isolated.
The lake appears to be situated about 20 kilometres from
Mungo River as the crow flies, and about twice as far from
the nearest sea-shore. Mr. Dusén puts its altitude above the
sea-level at 90 m. In these circumstances it is therefore
the more interesting to find that it has a fish-fauna consisting
of at least five species of Cichlide, which have been sent to
me by Mr. Linnell, namely :-—
Hemichromis fasciatus, Peters.
A small specimen.
Pelmatochromis longirostris, Boulenger.
A specimen in good condition.
Tilapia macrocephala (Bleeker).
A fine large specimen, measuring 189 mm., with quite
normal dentition.
Tilapia kotte, sp. n.
Scales cycloid, without marginal denticulations. About
10 gill-rakers on "lower part of anterior arch, An outer series
of ieetb of moderate size, two or three inner series of very
* Geol, Foren. Forh. no. 155, Bd. xvi. (Stockholm, 1894).
136 Dr. E. Liénnberg on Fishes from the
minute teeth. Depth of body 23 to 22 in total length with-
out caudal. Length of head 22 (in younger) to 24 times (in
older specimens) in total length. Snout and forehead with
straight upper profile, forming a distinct although blunt angle
with the outline of the back. Diameter of eye contained
1} (in younger) to 1} times (in older specimens) in length of
snout, 3} (in younger) to 4 times (in older) in length of head,
1} to 14 in interorbital width. Maxillary extending almost
to the vertical through the anterior border of the eye. Three
series of scales on the cheeks; opercle with large scales.
Dorsal XV (XVI in one specimen) (11-) 12; last spine longest,
4 to 4 length of head; middle soft rays produced 14 times as
long as longest dorsal spine. Pectoral not extending to origin
of anal, pointed, but in all specimens a little shorter than head.
Ventral produced, usually reaching vent or a little beyond.
Anal III 8, third spine shorter than last dorsal; soft rays
produced 13 times as long as third anal spine. Caudal
truncate or a little emarginate. Scales cycloid, 26-27 7" ;
lat. line 229. Very faint traces of four or five dusky hairs
may be seen in some specimens, in others not. A black
opercular spot always present, and a blackish spot at the base
of the anterior soft rays of the dorsal. Anal often more or
less dusky to blackish ; in the latter case, the chin, lower jaw,
ventrals, and more or less of the opercle and belly as well as
lower half of the caudal are blackish to black. In some speci-
mens roundish light spots surrounded by dusky are seen on
the posterior part of the soft dorsal and upper half of the
caudal. ‘The black-bellied specimens are smaller, but have a
larger anal papilla, and an examination of the interior
proves that they are males. ‘The larger specimens with
light-coloured belly are females. As the genital organs do
not contain ripe products, it is evident that the sexual
difference in colour is constant, and not confined to the
breeding-season. ‘The males measure 10 to 12 cm. in length,
the females 124 to 14 cin.
Iam much indebted to Mr. Boulenger, who has kindly
sent me a specimen of Tilapia Zillit (Gervais) from Lake
Menzaleh, Egypt, which he regards as most nearly related
to the Yilapia from Lake Barombi-ba-kotta. There are,
however, several characteristics that show these two fishes
to be quite distinct from each other. The shape is different :
in JT. Zillitd the profile forms an even bow without the
pronounced nuchal angle of 7. kotte; in the former species
the soft rays of the dorsal and anal fins are much more
produced, so that they are about twice as long as the
Lakes of the Cameroon Mountain. 137
longest anal spine. The number and arrangement of scales
also differ; for instance, in 7. Zillit there are 4-34 scales
between the lat. 1. and anterior dorsal spines, and 24 between
the posterior end of lat. 1. and the dorsal, whereas in 1’, kotte
the same numbers are 3 and 14. The proportions are also
dissimilar : in two specimens of exactly the same length the
head of 7. kotte is 36 °/, and that of 7. Zilhit only 31 °/, of
the total length without caudal. The colour is also different,
as T. Zillii has 6 to 8 dark bars and sometimes a longitudinal
stripe. All these particulars, together with the geographical
separation, induce me to establish a separate species, named
after Lake Barombi-ba-kotta. According to Mr. Boulenger,
T. Zillit is distributed from the Algerian Sahara to Lake
Rudolph and the Lake of Galilee.
From the Yvlapia lata group, T. kotte is distinguished
by its shorter pectorals &e.
Mr. Linnell has obtained quite a number of specimens of
T. kotte, so that the above description is based on several
examples.
Tilapia dubia, sp. n. ?
It is with much hesitation that I propose this new species,
as it is based on only one specimen ; but, on the other hand,
its markings are so distinct, and it differs so decidedly from the
species of Zilapia to which it might otherwise be related,
that it seems incorrect not to describe it separately.
An outer series of rather large and only slightly notched
teeth, about 14 on each side of the upper jaw; on the inner
side of this outer row two or three series of minute teeth.
Depth of body 2 times in total length without caudal, length
of head 3 times. Snout with straight upper profile, as long
as diameter of eye, which is contained 3 times in length of
head and 12 times in interorbital width. Maxillary extend-
ing to between nostril and eye. Three series of scales on the
cheek ; large scales on the opercle. Giull-rakers short, 13-14
on lower part of anterior arch. Pectoral pointed, much longer
than head, and extending a good deal beyond the origin of
anal. Ventral not produced reaching vent but not beyond.
Dorsal XVI 13, spines subequal from the fifth, about } length
of head. Anal ILI 10, third spine stouter than dorsal spines,
but of nearly the same length. (Caudal mutilated.) Caudal
peduncle nearly 14 as deep as long. Scales cycloid, probably
about 27-28 =, lat. lin. =. An opercular black spot, another
at the base of the anterior soft rays of the dorsal. Hight dark
bars, the first just in front of the opercular spot, the second
138 Dr. E. Lénnberg on Pishes from the
from the foremost dorsal spines, the fifth from the dark spot
of soft dorsal, the sixth at the end of the dorsal, and the
eighth at the base of the caudal. Anal and ventrals dusky
to blackish. ‘Total length with the caudal probably about
82-85 mm.
This form is evidently closely allied to T. Marie, Bou-
lenger, with which it agrees in relative dimensions of head
and body, number of rays of vertical fins, and exterior
markings. The differences are found in the dentition (as
Mr. Boulenger says* respecting 7. Marie, “teeth small, in
three series’), and in the shortness of the pectoral in the last-
mentioned species, in which it is only as long as head and
does not extend to origin of anal. On the other hand, the
ventrals of J. Marie are longer and reach origin of anal.
‘That species has also four series of scales on the cheek. It
should also be mentioned that Boulenger’s specimens were
about the same size as mine, so that the differences are not due
to age.
T’. Biittikoferi (Hubrecht) seems also to resemble this form
in having eight dark bars and similar relative proportions.
The teeth of the outer row in that species are also similarly
enlarged; but JZ’. Buttikofert differs in having “ 5 or 6 series
of scales on the cheek,’ smaller number of spines but larger
number of soft rays in the dorsal, shorter pectoral (subequal
to or shorter than head, not extending to origin of anal),
and longer ventral as in 7, Marie. To unite these appears
therefore impossible or only apt to cause confusion. When
these fishes become more perfectly known, it may be possible
to place some series of forms together as subspecies under
one and the same species; but this seems rather early yet,
and therefore it is best to collect as much knowledge as
possible by carefully describing the different varieties.
From the Elephant Lake only one species has been added
to the collection t, but it is of interest as being new to
science. Itis a Barbus of the B. Bynni group, aud I propose
to call it
Barbus Linnellit, sp. n.
Depth of body 34 to nearly 4 (8,95) times in total length
* In his very valuable paper ‘ A Revision of the African and Syrian
Fishes of the Family Cichlidee.—Part II.,” Proc. Zool. Soc. London,
1899, p. 98.
+ Mr. Linnell informs me that Mr. Rithke, of the German station,
Johann Albrechtshéhe, helped him to procure this fish from the
Elephant Lake.
Lakes of the Cameroon Mountain. 139
without caudal; length of head 33 to 33 times in total length.
Snout rounded, 24 times (or slightly more) in length of head.
Diameter of eye (of these large specimens) 6 to 64 times in
length of head. Interorbital width about equal to length of
snout, thus about 24 to 22 times in length of head. Mouth
inferior ; lips well developed, lower continuous. Barbels two
on each side, the posterior a little longer than the anterior,
exceeding the latter by a fourth or a fifth of its length ;
the anterior is equal to diameter of eye ora little (4 to =4)
longer, the posterior is 14 times diameter of eye; the distance
between the barbels is quite intermediate between the length
of anterior and posterior barbels. Dorsal III 9; last simple
ray rather strong, bony, not serrated, slightly curved, a little
more than half as long as head (55 °/,) ; free edge of the fin
emarginate, its distance from the occiput less than its distance
from the caudal. Anal III 5, longest anal ray decidedly
longer than longest dorsal ray, and measuring 3 (68 °/,)
length of head. Pectoral about ? length of head, not reach-
ing ventral, latter below anterior part of dorsal. Caudal
peduncle 14 to 1} times as long as deep. Scales 20-27 >,
2 (or 24) between lateral line and root of ventral, 12 round
caudal peduncle. Two specimens, respectively 360 and
435 mm. in length.
This Barbus is no doubt nearly related to B. Batesi,
Boulenger, but differs from that species in several respects.
Since Mr. Boulenger described * B. Batesiz on a single speci-
men from Kribi River, Southern Cameroons, he has received
several specimens from 185 to 340 mm. long, and he has in the
most friendly way favoured me with a fresh description (for
which I owe him my best thanks) of this species, based on
the increased material. A comparison with this description
reveals that Barbus Linnellii differs from B. Batesiz in several
particulars. The former has a comparatively larger head and
longer snout. Its interorbital width is larger, but the barbels,
and the distance between them, when compared with the
diameter of the eye are smaller. The dorsal is lower, but the
anal is rather higher when compared with the length of
the head. The scales are fewer in number and larger, as
may readily be seen. ‘lhe two forms must therefore be kept
distinct, even if Barbus Linnellit of the Elephant Lake be
regarded as derived from B. Batesi¢ through isolation.
The Museum, Gothenburg,
Jan. 6th, 1904.
* Proc. Zool. Soc. 1908, vol. i. p. 25,
140 Mr. H. H. Druce on new
XVI.—Descriptions of new Species of Lycxnide from Borneo
and New Guinea. By Hamitron H. Drucs, F.Z.S.,
ELE.S.
Thysonotis hebes, sp. 1.
3 .—Upperside. Allied to T. Piepersii*, from which it
differs by its smaller size, by being of a darker and more
purple shade of blue, and by the outer margins of the fore
wing being even more broadly black, especially towards the
anal angle.
Underside differs from that of T. Piepersid by the almost
total absence of the yellow basal streak on the costa of the
fore wing and the absence of the metallic green borders to
the black lunules in the border of the hind wing. There are
a few metallic scales at the base of the hind wing and about
halfway along the costa from the base.
Thorax black ; palpi black, clothed with whitish hairs at
the base; abdomen black, ringed with blue scales at each
seement; legs black, with grey scales at joints.
Expanse 1} inch.
Hab. Upper Aroa River, British New Guinea (Meek,
Mus. Druce).
The two specimens we possess were captured in January
and February.
Candalides pruina, sp. n.
3 .—Upperside. Uniform deep black, with the costal half
of the fore wing from the base nearly to the outer margin
dark, shining, hoary purple, with the costal margin and the
nervules narrowly black, and a central patch of differently
placed scales lying principally on the median nervure and on
the bases of the median nervules. When held at an angle
the black hind wings show a slight olivaceous tinge. The
cilia of the fore wing are black, slightly whitish at the angle,
as is also the apex of the hind wing, which is again distinctly
white along the abdominal margin, widening out to a small
white patch at the base of the abdominal fold.
The underside is marked exactly like that of C. stlicea +,
but the black spots are slightly fainter and the apex and
costa appear very slightly suffused with greyish.
* Cupido Piepersii, Snellen, Tijd. Entom. xxi. p. 16, pl. i. fig. 5 (1878).
+ Holochila silicea, Grose-Smith, Novitates Zoolog. 1. p. 580 (1894) ;
Rhop. Exot. ii., Orient. Lye. ix. Holochila, 1. figs. 6, 7, 8 (1896). —
Lycenide from Borneo and New Guinea. 141
Head, thorax, and abdomen black above, whitish beneath ;
palpi white, tipped with black; legs black and white.
Expanse 1,%,-12 inch.
Hab. Upper Aroa River, British New Guinea (Meek,
Mus. Druce).
‘The two specimens we possess were captured, one in January
and one in February.
Not nearly allied to any described species.
Tajuria lucullus, sp. n.
3 .—Allied to 7. cato *, from which it differs on the upper-
side by being of a more silvery shade of blue and by the blue
area on the fore wing extending right up to the anal angle,
but not reaching to the upper wall of the cell as in that
species. The lobe on the hind wing is considerably smaller,
with its black spot larger and the orange crown very
indistinct.
On the underside the ground-colour is slightly paler than
in J. cato and in the fore wing the dark transverse line
commences near the costal margin, further from the apex
than in that species, and runs almost straight nearly to the
inner margin; in the hind wing the dark line is also placed
further inwards and the orange blotches near the anal angle
are darker, more condensed, and larger than in J. cato. The
lobe itself is entirely black and the space above the sub-
median nervure is entirely covered with shining pale blue
scales. The black spot between the lower median nervules is
larger.
There are indistinct lines closing the ends of the cells in
both wings which are absent in J’. cato.
Thorax and abdomen bluish above, pearly grey below ;
legs black, with whitish spots ; antennee black above, spotted
with white below.
Expanse 1¢# inch.
Hab. Kina Balu, Borneo (Mus. Druce).
This insect is closely allied to 7. cato, but is at once distin-
guished by the characters enumerated above.
One specimen only, in fine condition.
Tajuria stigmata, sp. 0.
gd .—Allied to Tajuria berenis t, but differs by being
smaller, by the blue on the upperside being darker and of a
* Tajuria cato, H. H. Druce, P. Z. 8. 1895, p. 601, pl. xxiii. figs. 14, 16,
+ Tajuria berenis, H. H. Druce, P. Z. S. 1896, p. 674, pl. xxi. fig. 6.
1492 Mr. O. Thomas on
more violaceous hue, and by the possession of a large oliva-
ceous brown band occupying the upper end of the cell and
reaching to the black apical border, The lobe is much
smaller and black.
On the underside the ground-colour is much as in 1. be-
renis, but the transverse lines are placed further inwards from
the margins and are much straighter. There are no faint
lines closing the cells of both wings, as in T. berenis, and the
orange patches at the anal angle of the hind wing are paler,
more extensive, and not separated by the submedian inter-
space, as in 1’. berenis. he black lobe is crowned with
shining silvery-blue scales.
9 .—Upperside differs from male only by the disk of the
fore wing being of a slightly paler blue, the apex being less
broadly black, and by the total absence of the olivaceous
brand.
On the underside the dark transverse line is more con-
spicuous and more distinctly edged outwards with whitish
than in the male.
Head, thorax, and abdomen bluish above, pearly white
below ; legs white-spotted ; antenuz minutely white-spotted.
Expanse 12 inch.
Hab. Kina Balu, Borneo (Mus. Druce).
Distinguished at once from all others of the group by the
large brand in the male, which may necessitate the erection of
a new genus to contain it.
XVIT.—Two new Mammals from South America.
By OLpFIELD ‘THOMAS.
Oryzomys oniscus, Sp. n.
A medium-sized species allied to O. intermedius and
O. laticeps.
Size about as in O. intermedius, therefore larger than in
O. laticeps. Fur close and rather short; hairs of back barely
10 mm. in length. General colour of upper surface dark
greyish tinged with buffy, the resulting tone being rather .
paler than Ridgtvay’s “ bistre ” and very near that of certain
of the darker forms of the laticeps group, e. g. O. perenensis,
Allen. Median area of back noticeably darker than rest.
Sides rather, but not conspicuously, more buffy. Whole of
under surface and inner sides of limbs greyish white (“ grey
new Mammals from South America. 143
no. 9’), the bases of the hairs slaty, the tips white. Line of
demarcation on sides fairly well defined. Head like body ;
muzzle rather darker, with dark rims round the eyes. Lars
rather large, thinly haired, greyish brown. Outer surface of
arms and legs drab-grey ; hands and feet pure white. ‘Tail
approximately equal in length to the head and body, very
finely scaled, practically naked ; greyish brown, rather paler
for its proximal third below.
Skull closely similar in size and shape to that of O. c¢nter-
medius, therefore decidedly larger than in O. laticeps; the
palatal foramina are, however, rather shorter than in the
former, though not so short as in the latter, and are more
widely open. The supraorbital edges are squared or finely
beaded, but are without overhanging ledges.
Dimensions of the type (measured in the flesh) :—
Head and body 140 mm. ; tail 145 ; hind foot, s. u. 31
(range 80-833), c. u. 83; ear 24.
Skull: greatest length 36°3; basilar length 28; greatest
breadth 18°5; nasals 13°7; interorbital breadth 5°63; palate
length 15°6; palatal foramina 5:1 x2°6; length of upper
molar series 5.
Hab. S. Lourengo, near Pernambuco. Alt. 50 m.
Type. Adult male. B.M. no. 3. 10. 1. 42. Original
number 1573. Collected 23rd July, 1903, by Alphonse
Robert. Hight specimens.
This Oryzomys is readily distinguished from any species
hitherto known. In its colour it is remarkably like some of
the forms of the O. laticeys group, but is separable from
them by its much larger skull and longer palatine foramina.
In some of the specimens the darker dorsal area is so marked
as to suggest an affinity with O. sublineatus, Vhos., but the
hind feet in that species are conspicuously shorter.
From O. physodes, Licht. (Rio Janeiro and Espirito Santo),
O. lamia, Thos. (Minas Geraes), and O. intermedius, Leche
(Sao Paulo to Rio Grande do Sul), of all of which Mr. Robert
has obtained specimens, this species in distinguishable by
the absence of the rufous or buffy body-colour found in those
animals.
Marmosa germana, sp. n.
A large species of the cinerea group, with a wholly brown
tail.
Fur thick, close, and wavy ; hairs of back about 10-11 mm.
in length. General colour above pale brown, rather paler
than “mummy-brown,” rather less yellow than “raw
umber” of Ridgway. Under surface soiled buffy greyish,
144 Dr. W. T. Calman on the
the hairs slaty, with pale buffy tips. Crown of head like
back. Dark orbital rings broad, strongly marked, extending
forwards on to the sides of the muzzle. Cheeks and chin
clearer buffy. Outer sides of arms and legs like back, inner
sides like belly; hands and feet practically naked, pale
brownish. ‘Tail furry at its base for a shorter distance than
usual, the fur, which is coloured like that of the back, ex-
tending for only about an inch and being surpassed posteriorly
by the outstretched feet ; remaimder of tail naked, as usual,
but instead of being white terminally it is umformly pale
brown to the end, at least above, the under surface being in
one specimen slightly paler terminally.
Skull with well-expanded zygomata and broad interorbital
region, with overhanging postorbital ledges. ‘Teeth large,
of the usual proportions in this group.
Dimensions of the type (measured in skin) :—
Head and body 187 mm. ; tail 245; hind foot (s. u.) 23;
ear 19.
Skull: basal length 39°5; greatest breadth 25; nasals
18°5 x 6:2; interorbital breadth 7:6; breadth across _post-
orbital processes 9°4; breadth of brain-case 15; palate -
length 23°5 ; combined length of three anterior molariform.
teeth 7°7.
Fab. Sarayacu, Oriente of Ecuador.
Type. Female (young adult). B.M. no. 80. 5. 6. 77.
Collected by Mr. Clarence Buckley. An old male also in
collection.
This opossum shares with M. regina * alone of the present
group the distinction of having a wholly brown tail, not
turning to white at its end. From that species it is separated
by its duller and less yellowish belly-colour, broader skull,
and larger molars.
XVIII.—On the Classification of the Crustacea Malacostraca.
By W. T. Caiman, D.Sc.
In the course of preparing a general account of the Crustacea
for a forthcoming volume of Prof. E. Ray Lankester’s
‘Treatise on Zoology’ I have been led to discard the com-
monly accepted classification of the Malacostraca and to
adopt a scheme which was briefly outlined by Dr. H. J.
Hansen some ten years ago. The object of the present
* Ann. & Mag. Nat. Hist. (7) ii, p. 275 (1898).
Classification of the Crustacea Malacostraca. 145
paper is to discuss somewhat more fully than is possible
within the limits of a text-book certain of the facts bearing
upon the case, to put into systematic form (with some modifi-
cations and additions) the classification suggested by
Dr. Hansen, and to invite criticism of the result.
In 1815 Leach *, adopting a basis of classification which
had previously been applied by Lamarck to the whole class
of Crustacea, divided the subclass Malacostraca into two
legions—the Podophthalmaand the Edriophthalma—according
to the condition of the eyes, movably pedunculate in the one
and sessile in the other. Without attempting to summarize
the numerous modifications which have been suggested, it
may be said that Leach’s classification has been accepted in
principle by the majority of carcinologists since his time, and
is that most generally followed at the present day. As
originally defined, the two groups were sharply distinguished
from each other not only by the characters given by Leach,
but also by the presence in the Podophthalma of a cephalo-
thoracic shield or carapace which was absent in the EKdrio-
phthalma, this character giving occasion for the names
Thoracostraca and Arthrostraca applied to them by Bur-
meister. The progress of research, however, rendered it
increasingly difficult to form satisfactory definitions of the
two divisions. In particular the recognition by Fritz Muller
of a true, though reduced, carapace in the Tanaide and the
elucidation of the structure of the Cumacea begun b
H. Goodsir and by Kroyer provided intermediate links, the
Cumacea, indeed, being placed sometimes in the one group
and sometimes in the other. Claus { established a third
division (Leptostraca) for Nebalia and its allies, and the
separation of the Stomatopoda from the other Podophthalma,
first suggested, I believe, by Huxley §, left in the last-named
group only the Schizopoda and Decapoda.
An important departure from the line of classification
generally followed was made in 1883 by Prof. Boas|l, who
abandoned the group Schizopoda, pointing out that the Myside
and Lophogastride were by no means closely related to the
* “A Tabular View of the External Characters of Four Classes of
Animals which Linné arranged under Insecta..... »” Trans. Linn. Soe,
London, xi. (1815) pp. 806-400.
+ ‘Beitraige zur Naturgeschichte der Rankenfiisser, Berlin, 1834, p. 55.
t ‘ Grundziige der Zoologie,’ 4te Aufl. (1880) p. 573.
§ Introd. Classification Anim. (1869) p. 125; Manual Anat. Invert.
Animals (1877), p. 317.
|| “ Studien tiber die Verwandtschaftsbeziehungen der Malakostraken,”
Morphol. Jahrb, viti. pp. 485-579, pls. xxi.-xxiv. (1883).
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 10
146 Dr. W. T. Calman on the
BKuphausiide, with which they had until then been associated.
Boas divided the Malacostraca into seven orders—the Huphau-
siacea, Mysidacea, Cumacea, Isopoda, Amphipoda, Decapoda,
and Squillacea. This view was severely criticised by Claus”,
who, while admitting points of affinity between Myside and
Arthrostraca on the one hand, and between Kuphausiide and
Decapoda on the other, retained the Schizopoda as a central
and primitive group, and classed them along with the
Decapoda as Thoracostraca.
In 1893 Dr. Hansen +t, in a preliminary account of his
researches on the morphology of the appendages in Insects
and Crustacea (not yet published in full), proposed a still
further modification of the classification on the lines laid down
by Boas, from whom, however, he differs on many points.
While agreeing in discarding the group Schizopoda, Hansen
points out that the Enphausiacea do not occupy the primitive
position assigned to them by Boas, and he emphasizes their
close affinity with the Decapoda, with which he proposes to
associate them, opposing to the group thus formed another of
equal rank, comprising the Mysidacea, the Cumacea, and
the Edriophthalmate orders. Hansen’s proposals seem to
have attracted little attention, and I am not aware that any
writer has adopted the classification suggested, though to me
this arrangement of the Malacostraca appears to be the only
one which adequately expresses our present knowledge of
their morphology.
As Dr. Hansen does not give any names to the two groups
which he defines, it may be convenient to state here that I
propose the names PERACARIDA (m7pa, a pouch) for the
division which includes the Mysidacea, Cumacea, Tanaidacea,
Isopoda, and Amphipoda, and Kucartipa for the Huphausi-
acea and Decapoda.
From this it will be seen that the chief point on which
there is divergence of opinion is the retention of the Schizopoda
as anatural group. That the Mysidze present affinities with
the Edriophthalma and the Kuphausiides with the Decapoda
is not disputed; but if we adopt Claus’s view that the
Schizopoda are a central group approximating to the stock
from which the other orders have been derived, there is
nothing to forbid their association with the other Podo-
phthalma in our taxonomic arrangement. When, however,
* “ Neue Beitrage zur Morphologie der Crustaceen,’” Arb. Zool. Inst.
Wien, vi. pp. 1-108, pls. i—vi. (1885).
+ “Zur Morphologie der Gliedmassen und Mundtheile bei Crustaceen
und Insecten,” Zool. Anz. xvi. pp. 193-198 & 201-212, Translated in
Ann. & Mag. Nat. Hist. (6) xi. pp. 417-454 (1895),
Classification of the Crustacea Malacostraca. 147
we come to compare the characters (as given, for instance, by
Sars *) of the Euphausiide on the one hand, with those of
the Mysidw, Lophogastride, and Hucopiide on the other, we
find that, with one important exception, to be discussed
presently, the two groups do not agree in one single character
which they do not share with the lower Decapods, and for
the most part also with the Stomatopoda and Leptostraca.
They agree in possessing a carapace, movable eyes, a scale-
like exopodite on the antenna, an elongated and ventrally
flexed abdomen, and a “ tail-fan”’ formed by the lamellar
rami of the last pair of appendages displayed on either side
of the telson. This combination of characters goes to make
up what might be called the caridoid “ facies,” and at first sight
strongly suggests affinity between the groups exhibiting it.
It seems reasonable to suppose, however, that these characters,
together with such others as the natatory exopodites of the
thoracic limbs, are precisely what we must attribute to the
hypothetical stock of the Malacostraca, and that the caridoid
form has been retained in each of the divergent branches
proceeding therefrom by those members which have adhered
most closely to the primitive habits of life, and especially of
locomotion, That the stalked eyes and the carapace are
primitive features is not now disputed, nor can it be doubted
that the possession of an exopodite on the antenna is also
primitive, though it has been lost by the Leptostraca. The
lamellar form of this exopodite is intelligible as an adaptation
to swimming habits, and its reduction or loss corresponds
fairly closely in most cases with diminished natatory powers.
The fan-like disposition of uropods and telson is another
character not shared by the Leptostraca, which, nevertheless,
was probably possessed by the primitive Malacostraca, since
it occurs in the lower Decapoda and the Stomatopoda, and
also, though more or less modified, in Cumacea and many
Isopoda. The retention of these primitive characters does
not necessarily imply any special affinity between the various
groups which exhibited them.
The one character, above referred to, which is stated to
distinguish all Schizopoda from the Decapoda is the freedom
of the terga of one or more of the posterior thoracic somites
from the carapace. In the Mysidz, Lophogastride, and
Euccpiide at least five of these somites are complete upon
the dorsal side and distinct from, although more or less over-
lapped by, the carapace. It has been stated that in the
luupuausiide the last thoracic somite remains distinct, while
* Rep. Schizopoda ‘ Challenger,’ pp. 10 & uf! wee
148 Dr. W. T. Calman on the
in the Decapoda all are coalesced with the carapace. If this
were so it would constitute a strong, though not conclusive,
argument in favour of retaining the Euphausiide in asso-
ciation with the other families of Schizopoda. As a matter
of fact, however, this difference between the Euphausiide
and Decapoda does not exist.
A
Junction of thoracic and abdominal regions of the body, from the dorsal
side. A. Nyctiphanes norvegica (Euphausiacea); B. Pandalus Bon-
niert (Caridea).
a, carapace ; 4, intermediate plate; ¢, tergum of first abdominal somite ;
d, tergum of second abdominal somite; e, articular surface defined
by a groove on surface of second somite. The thorax and abdomen
are drawn slightly apart, to show the area occupied by soft articular
membrane between (indicated by shading).
If the junction of thorax and abdomen in a. typical
Euphausid such as Vyctiphanes be compared with the same
region in one of the lower Decapoda (Peneeidea or Caridea), a
}recise similarity of structure is found (see figure). The poste-
rior margin of the carapace is concave on the dorsal side,
leaving between it and the apparent anterior margin of the first
abdominal somite an area of roughly lenticular outline, which
is fully exposed when the abdomen is flexed, and is occupied by
a firmly chitinized plate (}). Anteriorly this plate is overlapped
by the carapace, with which it is connected by soft articular
Classification of the Crustacea Mulacostraca. 149
membrane, and posteriorly it is firmly connected with the
first abdominal somite. It is to all appearance quite compa-
rable to thearticular surface (e) on the dorsal aspect of the other
abdominal somites, which is concealed beneath the posterior
margin of the somite in front when the abdomen is extended,
and it only differs from these articular surfaces in being more
sharply defined from the somite of which it forms a part.
It is possible, though I know of no evidence to support the
view *, that this plate is actually the tergal portion of the
last thoracic somite, which has become detached from the
sternal portion and has coalesced with the succeeding somite,
but, in any case, the structure is exactly alike in Euphausiide
and in the lower Decapods. I have carefully sought for
other evidence of a distinct tergal element of the last thoracic
somite in Kuphausiide, but without success, and I can only
conclude that the statement of its existence is an error based
upon the observation of this intermediate plate without direct
comparison with the Decapoda.
One point in which the Kuphausiacea appear to agree
with a section of the Mysidacea and to differ from the
Decapoda is the possession of a single series of branchise at
the bases of the thoracic limbs. In the Decapoda the gills
are arranged in several (typically four) series. Those of the
Kuphausiacea are attached to the coxopodites of the limbs,
corresponding to the podobranchiz (and epipodites) of the
Decapods, from which, however, they differ in their mode of
branching. In the Lophogastride and Eucopiide, on the
other hand, the gills are attached to the articular membrane
at the base of the limbs, and are, in fact, arthrobranchiz.
As Claus has pointed out, this difference in the place of
attachment does not necessarily invalidate the comparison
between the branchiz of the two groups, since he has shown
that in certain Decapods the arthrobranchize develop as out-
growths from the basal portions of the limbs, and that the
pleurobranchiz had in all probability a similar origin, There
is, however, another fact which may have a bearing on this
question. In Gnathophausia (Lophogastride) Sars describes
a small tongue-like process, tipped with a group of sete, on
the outer side of the coxopodite of all the thoracic limbs
except the first pair, and he regards this as a reduced epipo-
dite. It seems not unlikely that this process, and not the
gill itself, is homologous with the epipodial gill of the
* Williamson figures this plate as a separate sclerite in the larva of
Crangon, ‘On the Larval Stages of Decapod Crustacea——The Shrimp
( Crangon vulgaris, Fabr.),” Rep. Fishery Board Scotland, xix. (8) 1901,
pl. v. fig. 166, “ 27.”
150 Dr. W. T. Calman on the
Euphausiidee. On the assumption that the primitive Malaco-
straca possessed at least two epipodial appendages on each
thoracic limb (as in Anaspides), the distal series may have
become modified as branchize in the Euphausiide and the
proximal in the Lophogastride. In any case, the form of
the gills differs considerably in the two cases, and the only
point which they have in common as against the Decapoda is
the arrangement in one instead of several series.
Among the characters in which the Mysidacea differ from
the Huphausiacea and agree with the Edriophthalmate orders
the most conspicuous is the possession by the female sex of
a brood-pouch or marsupium, in which the eggs and young
are carried. It cannot be doubted that this structure is
homologous throughout the whole series which I have na:ne],
from this feature, the Peracarida, in spite of real or alleged
differences in the mode of its development. It is formed by
a series of overlapping plates (which Claus considers, with
great probability, to be of the nature of epipodites) attached
to the inner side of the coxopodites of some or all of the
thoracic limbs. When, as in many Isopoda, the coxopodites
are fused with the body, the plates are attached to the sternal
surface of the somites. In some cases these plates or oostegites
develop as bud-like outgrowths from the bases of the limbs,
increasing in size at successive ecdyses as sexual maturity 1s
approached; but in certain Isopoda it has been shown that the
course of development is abbreviated, the oostegites growing in
the space between the sternal cuticle and the hypodermis, and
being set free, completely formed, at a single moult *.
Probably some similar process has given rise to the statement
that the oostegites arise by splitting of the ventral cuticle in the
Cumacea } and in the Isopod Gnathiaf. At the same time
it is certain that the formation of the brood-pouch is profoundly
modified in certain parasitic Isopods of the tribe Epicaridea.
In many of these the oostegites develop in the typical fashion
just described, but in the more specialized forms the structure
is very different and hard to understand. In Hem/oniscus,
where the development has been worked out in detail by
Caullery and Mesnil §, the marsupial. cavity is hollowed out
* Cf. Leichmann, “ Beitr. z. Naturgesch. d. Isopoden,” Bibl. Zool. x.
(1891).
+ G. O. Sars, “Beskr. af de ‘paa Freg. Josephines Exp. fundne
Cumaceer,” Kongl. Svenska Vet,Akad. Handl. ix. 13 (1871), p. 19.
t Dohrn, “ Entw. und Organ. v. Praniza (Anceus) mavillaris,’ Zeitschr.
f. wiss. Zool. xx. (1870) p. 70.
§ “ Recherches sur ?Hemioniscus balant, Buchholz....,” Bull. Sei.
France et Belgique, xxxiv. pp. 316-362, pls. xvil. & xviii, 5 fige. in text
(1901).
Classification of the Crustacea Malacostraca. 151
in a thickening of the ectoderm on the sternal surface, and is
from the first completely closed. Further research will be
required to show what relation this cavity bears to the normal
marsupium.
Apart from such exceptional cases, however, the possession
of oostegites is a character quite peculiar to the group of
orders included in the Peracarida and not found in any other
Crustacea. It is true that the Euphausiide are described as
carrying their eggs in sacs attached to the sternal surface of
the thorax, and it has been assumed that these represent the
marsupium of the Mysidacea. But, as Sars * has pointed
out, the “ ovisacs ” are apparently formed by the consolidation
of some cementing substance which is extruded along with
the eggs from the oviducts. The rarity of ovigerous specimens
would suggest that the eggs are so carried for only a_ brief
period, while in some of the commonest species they have
never yet been observed. This last circumstance is explained
by an interesting observation for which I am indebted to
Mr. E. W. L. Holt. In Huphausia pellucida Mr. Holt
finds that the eggs when expelled from the body are not
agglutinated together in masses, but are simply carried for a
time between the thoracic feet of the female. In Nyctiphanes
Couchit the egg-sacs have long been known. By the kindness
of Mr. Holt I have been enabled to examine well-preserved
specimens of both these species, and I find that, as, indeed, is
implied by Sars’s account, the structures found in V. Couchit
are more properly described as egg-masses than as sacs, there
being no definite enc'osing membrane, but simply a tilm of
hardened cement which also penetrates between and holds
the eggs together. It is plain that this structure bears no
morphological relation to the oostegites of the Peracarida. A
very similar arrangement is found in the Decapod Leuczfer,
where, according to Brooks ¢, the eggs are “attached in a
loose bunch of twenty or more to the last pair of thoracic
limbs.”
A feature which is very characteristic of the Peracarida,
and one on which Boas and Hansen lay considerable stress,
is found in the structure of the mandibles. In all the orders
composing the series, with exceptions in the case of parasitic
and other secondarily modified forms, an accessory blade, the
lacinia mobilis of Hansen f, is developed just behind the
* Rep. Schizopoda ‘ Challenger,’ p. 118.
+ “ Leucifer, a Study in Morphology,” Phil. Trans. elxxiii. (1882) p. 60,
{ The term lacinza mobilis was first applied by Hansen (‘ Dijmphna
Togtets Zool. Bot. Udbytte ’ (1887), p. 197) to the accessory blade alone,
but. he afterwards extended its meaning to include also the row of spines
152 Dr. W. T. Calman on the
cutting-edge, and is followed by a row of serrated spines
extending towards the molar process. In the Huphausiide
and Decapoda no lacinia mobilis is found in the adult, though
in the Jarvex of both a group of serrated spines is sometimes
present, which disappears in the course of development.
Even in the adults of some of the more primitive Decapods,
for instance in certain Atyide *, a tuft or row of stout bristles
is found just below the cutting-edge, and it seems probable
that this is a vestige of the spine-row of the Peracaridan
mandible.
In distinguishing the Peracarida from the Eucarida,
Hansen attaches great importance to certain characters pre-
sented by the thoracic limbs. Boas had already pointed out
that the Myside and the Edriophthalmate orders have these
limbs terminated by a claw-like spine, which is absent in the
Euphausiacea and Decapoda. Hansen regards this claw as
representing a segment of the limb, and identifies it with the
minute terminal segment which he has discovered in the
Leptostraca. Boas had further indicated a difference between
the two groups in the direction of the articulations of the
limbs. In the Peracarida the ‘‘knee” or chief ventral
flexure of the leg is between the fifth and sixth segments,
counting from the base, while in the Hucarida it is between
the fourth and fifth. Hansen interprets this difference in the
following manner: he assumes that the position of the knee
is the same in both cases, that the apparent fourth segment
of the leg in Eucarida is equivalent to the fourth plus the
fitth in the Peracarida, and that the three segments beyond
the knee in the former case are homologous with the two
segments and the terminal claw in the latter. If this sug-
gestion be correct, we have a difference of a very marked
kind between the two groups. Dr. Hansen will doubtless
produce further evidence in its support when his researches
are published in full, but at present there are difficulties in
the way of adopting it as a basis for classification. In
certain primitive Isopoda (Janiride &c.) the leg terminates
in two, sometimes three, claws, not differing greatly in size
or perceptibly in structure, and it is difficult to believe that
one of them is to be regarded as the terminal segment while
the others are simply modified sete. Further, in many
which are often closely connected with it (“ Cirolanide,” Vidensk. Selsk.
Skr. (6) v. (1890) p. 276, footnote). In the present paper I have used the
term in its original and more restricted sense. :
* Cf. Calman, “ On Two Species of Macrurous Crustaceans from Lake
Tanganyika,” Proc. Zool. Soc. London, 1899, p. 705, pl. xxxix. fig. 6.
Classification of the Crustacea Malacostraca. 153
Peracarida the “claw ” is coalesced with the segment which
carries it, the suture-line between the two disappearing and
the place of junction being indicated, if at all, only by the
insertion of a minute seta, and it is not impossible that such
evidence of the existence of a “claw” may yet be found in
the terminal segment of the decapod leg. In the absence of
any definite proof that the fourth segment of the leg in
the EKucarida represents two fused segments, it seems better
to assume for the present that the segments of the legs are
serially comparable in the two groups.
Dr. Hansen includes among the characters of the Pera-
carida the presence of tubular processes for the orifices of
the vasa deferentia, which are stated to be absent in the
Eucarida. It is true that such processes are present in the
majority of the Peracarida, though they are sometimes much
reduced and may perhaps be altogether wanting in some
cases. ‘They are absent in the Kuphausiacea and in the
lower Decapoda, but in some Paguridea and in the Brachyura
the vasa deferentia terminate in tubular processes which are
often of considerable length.
The possession of spermatophores is another character on
which it seems unsafe to rely as distinguishing the Euphau-
siacea and Decapoda from the other orders of Malacostraca.
It certainly constitutes an important difference between the
Kuphausiacea and the Mysidacea, but it can hardly be ex-
tended without qualification to some of the other groups.
Prof. Gilson applies the term “spermatophores” to the
aggregations of spermatozoa found in certain Isopoda *, but
not to the sperm-masses of the Macrurat. The distinction
which Prof. Giard {| makes (in Insects) between spermato-
phores and “ spermotagmata,” according to the presence or
absence of a definite investing membrane, appears to be hard
to recognize among Crustacea and to have little systematic
importance §. On the other hand, the form of the spermatozoa
appears to afford constant and important characters differen-
tiating the two groups.
* “Etude comparée de la spermatogénése chez les Arthropodes,” La
Cellule, i. (1884) p. 153.
T Op. cit. 11, (1887) p. 187.
¢ “Sur la spermatogénése des Diptéres du genre Seciara,” C. R. Acad.
Sci. exxxiv. (1902) p. 1124.
§ Prof. McMurrich describes (‘‘ Embryology of the Isopod Crustacea,”
Journ. Morph. xi. 1895, p. 67) a very definite spermatophore in the Isopod
Jera in connexion with the process of “hypodermic impregnation ”
which he believes to occur in that genus; but his account is not very
detailed, and the phenomena which he describes are so remarkable that
further investigation is much to be desired.
154 Dr. W. T. Calman on the
With regard to these and other points of internal anatomy
our knowledge is very incomplete for many of the groups.
Nothing is known of the internal anatomy of the Lopho-
gastride, and very little regarding the Kuphausiide and
the lower decapods. One point which seems to tell against
the system of classification here advocated may be given for
what it is worth. This is the presence in all of the Podo-
phthalmate groups (Anaspides?, Myside, Huphausiide,
Decapoda, Stomatopoda) of an unpaired descending artery
originating from the posterior end of the heart or from the
base of the posterior aorta (superior abdominal artery) and
perforating the nerve-cord to become connected with the sub-
neural artery (sternal and inferior abdominal arteries). In
the Kdriophthaliate orders no similar arrangement is known,
the subneural artery, where it exists, being connected with
the dorsal portion of the vascular system by paired lateral
arteries or by a circumcesophageal ring. In view of the
great divergences which may exist in the disposition of the
arterial truuks within the limits of a single order (e.g. the
Isopoda), no great taxonomic importance can at present be
attached to such differences.
Besides the characters, summarized in the definitions given
below, which hold good throughout the various orders brought
together in this classification, there are many connecting
characters which serve to link together the individual orders
and to indicate their affinities, although they cannot con-
veniently be included in our definitions. Many of these are
discussed in the papers of Boas and Hansen, and we may
simply mention as examples the retroverted palp of the
maxillula in Lophogastride (Mysidacea), Cumacea, and
Tanaidacea, the branchial epipod of the first thoracic appen-
dage in the same orders, and the distinct, though immovable,
ocular peduncles of the ‘Tanaidacea. On the other side the
Euphausiacea share with some suborders of the Decapoda
the possession of an appendix interna on the pleopods, and
the elaborate copulatory armature of the first pair of pleopods
in the former group recalis that of the Penzeidea in the latter,
although differing in details. ‘The larval development of
the Euphausiacea runs closely parallel to that of the Penzidea,
aud Dr. Hansen’s recent discovery * in a species of Sergestes
of luminous organs resembling, though of somewhat different
structure from, those of the Muphausiacea, helps still further
to diminish the narrow space which separates the two.
* Proc. Zool. Soc. London, 1903, i. p. 72.
dD
Or
Classification of the Crustacea Mul.icostraca. 1
Since the papers of Boas and Hansen were written, the
necessity for a rearrangement of the Malacostraca has been
rendered still more urgent by Mr. G. M. Thomson's *
discovery of Anaspides. ‘This remarkable form presents a
combination of characters which indicate for it a very isolated
place in our classification. It is not merely a schizopod
without a carapace. ‘The double series of epipodial lamella,
the segmentation of the thoracic limbs, the double gnatho-
basic lobes of the first pair, and the apparent distinctness of
the first thoracic somite from the headf are among the
characters which remove it from close affinity with any
of the commonly recognized orders of Malacostraca.
Though Axaspides is not by any means like the hypothetical
ancestral malacostracan, its unmistakable resemblance to some
of the oldest fossil Malacostraca (Uronectes &c.) shows that
at least it is a very ancient type. In the classification given
below I have regarded Anaspides and its fossil allies as con-
stituting a division of equal rank with the Peracarida and
Eucarida. For this I have adopted the name Syncarida,
formerly proposed by Packard for the fossil forms alone.
The details which Mr, Thomson has given of the internal
anatomy of Anaspides are very remarkable, and further in-
vestigation on this point is much to be desired. Unfortu-
nately no specimens have yet reached this country in a state
of preservation suitable for anatomical purposes. The mode
of development is also quite unknown.
With regard to the other orders little need be said here.
Claus’s investigations on Nebalia leave no doubt that the
* “On a Freshwater Schizopod from Tasmania,” Trans. Linn. Soc,
London, (2) Zool. vi. pp. 285-395, pls. xxiv.-xxvi. (1894). Cf.alsoCalman,
“On the Genus dAnaspides and its Affinities with certain Fossil Crustacea,”
Trans. Roy. Soc. Edinburgh, xxxviii. (4) pp. 787-802, 2 pls. (1896).
+ I formerly suggested (Trans. Roy. Soc. Edinb. xxxviii. pt. 4, p. 787)
that the “cervical groove” of Anaspides, which was described by
Thomson as marking off the first thoracic somite from the head, really
represented the line of junction of the mandibular with the maxillular
somite, on the ground that owing to the forward direvtion of its lateral
portions the lower ends come to lie just behind the mandibles. I am
now disposed to doubt the correctness of this view. There appears to
be a tendency in those Malacostraca which are without a carapace for the
lateral plates (pleural or coxal) of the anterior thoracic somites to become
displaced forwards at their distal ends as if to protect the mouth-parts :
this is well seen in some Arcturide, for instance. It seems quite likely
that this groove in Anaspides has undergone a similar displacement, and
that it really does define the first thoracic somite, which is not distinet in
any other Kumalacostraca.
{ Especially “ Ueb. d. Organismus d. Nebaliden und d. syst. Stellung
d, Leptostraken,’” Arb, Zool. Inst. Wien, vil. (1889).
156 Dr. W. T. Calman on the
Leptostraca are intimately related to the Malacostraca, and
their position seems best expressed by Grobben’s * arrange-
ment, which divides the subclass into two main groups,
Leptostraca and Kumalacostraca.
‘The Stomatopoda must form a division of equal rank with
the Bucarida and Peracarida. To preserve the consonance
of names I propose to term it Hoplocarida. The morphology
of the members of this group has been somewhat neglected,
and their precise relationship to the other orders is by no
means clear. Their internal anatomy is imperfectly known
and would doubtless repay investigation f.
Classification here proposed.
Subclass MALACOSTRACA.
Series LEPTOSTRACA, Claus, 1880.
Division PHytLocaripa, Packard, 1879.
Order Nebaliacea, noy. nom.
Series EUMALACOSTRACA, Grobben, 1892.
Division Syncaripa, Packard, 1886.
Order Anaspidacea, nov.
Division PERACARIDA, nov. nom.
Orders Mysidacea.
Cumacea.
Tanaidacea.
Isopoda.
Amphipoda.
Division Evcaripa, nov. nom.
Orders Euphausiacea.
Decapoda,
Division HopLocaRIDA, noy. nom.
Order Stomatopoda.
Series LEPTOSTRACA.—Abdomen of seven somites, the
last of which is without appendages, and a telson bearing a
* « Zur Kenntniss des Stammbaumes und des Systems des Crustaceen,”
SB. Akad. Wien, ci. (1892) Abth. i. pp. 237-274.
+ Kowalevsky states (Biol. Centralbl. ix. (1889) p. 41) that the max-
illary gland (‘shell-gland”’) is greatly developed in the Stomatopoda,
but I cannot tind any description of it. Lhave observed on the posterior
surface of the maxilla in Sguil/a mantis a papilla with a minute terminal
pore which may be the aperture of the duct of this gland, but I have
had no opportunity of dissecting well-preserved specimens.
Classification of the Crustacea Malacostraca. 157
pair of movable articulated rami (caudal furca). An adductor
muscle runs transversely between the two valves of the
carapace. Thoracic limbs all similar, more or less foliaceous,
with protopodite of three segments.
Series EUMALACOSTRACA.—Abdomen of six somites
(the number may be reduced by coalescence), the last of
which typically bears a pair of appendages, and a telson
which never bears movable fureal rami*. No adductor
muscle of the carapace. Thoracic limbs rarely all similar
(Euphausiacea), typically pediform ; protopodite of two seg-
ments, except in Stomatopoda,
Division SyNCARIDA.—Carapace absent. All the thoracic
somites distinct. Eyes pedunculate. Antennal protopodite
of two segments. Mandible without lacinia mobilis.
Thoracic limbs flexed between fifth and sixth segments. No
oostegites. No appendix interna on pleopods. Hepatic
cxca numerous. Heart much elongated, tubular.
Division PERACARIDA.—Carapace, when present, leaving
at least four of the thoracic somites distinct. First thoracic
somite always fused with the head. Antennal protopodite
typically of three segments. Mandible with lacinia mobilis
(except in parasitic and other modified forms). ‘Thoracic
limbs flexed between fifth and sixth segments. Oostegites
attached to some or all of the thoracic limbs in female, form-
ing a brood-pouch. No appendix interna on_pleopods.
Hepatic ceca few and simple. Heart elongated, extending
through the greater part of thoracic region, or displaced into
abdomen. Spermatozoa filiform. Development taking place
within the brood-pouch ; young set free at a late stage.
Division EucartpaA.—Carapace coalescing dorsally with
all the thoracic somites. Eyes pedunculate. Antennal
protopodite with, at most, two distinct segments. Mandible
without lacinia mobilis in adult. ‘Thoracic limbs flexed
between fourth and fifth segments. No oostegites. An
appendix interna sometimes present on pleopods. Hepatic
exca much ramified. Heart abbreviated, thoracic. Sperma-
tozoa spherical or vesicular, often with radiating appendages.
Development as a rule with metamorphosis. A free-swimming
nauplius-stage in the more primitive forms.
* The movable appendages of the telson in Euphausiacea are modified
setee (Sars, ‘Challenger’ Rep., Schizopoda, p. 162),
158 Bibliographical Notices.
Division HorpLocartpA.—Carapace leaving at least four of
the thoracic somites distinct. ‘wo movable segments are
separated from the anterior part of the head, bearing respec-
tively the pedunculate eyes and the antennnles. Antennal
peduncle of two segments. Mandibles without lacinia mobilis.
Posterior thoracic limbs with protopodite of three segments.
(The relation of the segments of the anterior thoracic limbs
to those of the limbs in the other divisions is doubtful.)
An appendix interna on pleopods. Hepatic ceca much
ramified. Heart much elongated, extending through abdo-
minal and thoracic regions. Spermatozoa spherical. Deve-
Jopment with metamorphosis. No free-swimming nauplius-
stage.
BIBLIOGRAPHICAL NOTICES.
Memoirs of the Geological Survey of the United Kingdom.—The
Cretaceous Rocks of Britain. Vol. 11. The Lower and Middle
Chalk of Engiand. By A. J. Juxes-Browns, B.A., F.G.S. With
Contributions by Wrirtram Hitz, F.G.8. 8vo. Pages xiii and
568. With 93 Illustrations, including one Geological Map, two
Plates from photographs, and four from micrographs. E. Stan-
ford, London; J. Menzies, Edinburgh; and Hodges & Co.,
Dublin. 1903.
In the first volume of this series A. J. Jukes-Browne and W. Hill,
with others, described the Gault and Upper Greensand of England.
This second volume, by the same authors, together with many
contributors, deals with the Lower and Middle Chalk. The third
volume will include the description of the Upper Chalk, with
chapters on the economics of the soil, stone, &c., on the water-
supply, and the physical features of chalk districts, also a complete
catalogue of the fossils found in all the different divisions of the
Chalk. The present volume begins with a general and chrono-
logical account of the researches that led to the definition of the
several stratal divisions of the Chalk ; and in the sequel the zones
or horizons marked out by the occurrence of particular fossils are
carefully explained. This part of the book seems to have been
written before the valuable results of the researches by Rowe and
Sherborn were published; these and their subsequent work along
the cliff-sections of the Chalk will have greatly helped geologists in
the study of the strata and zones, and are largely utilized in the
chapters on the Middle Chalk.
The Lower Chalk (**Cenomanian ” in part) includes all the beds
Bibliographical Notices. 159
of marls and chalk between the Gault or Upper Greensand and the
Melbourn Rock, namely, the so-called ‘ Chloritic Marl” (and the
“ Cambridge Greensand ”), the “ Chalk Marl” (with the “ Tottern-
hoe Stone” in some districts), and the ‘Grey Chalk.” These are
subsequently described as to their characters, range, and fossils,
according to the several counties and the northern parts of France.
The Middle Chalk (or Turonian Stage) is defined as consisting of
zones marked by the occurrence of certain fossils, such as
3. Zone of Holaster planus, including the Chalk Rock.
2. Zone of Terebratulina gracilis.
1. Zone of Rhynchonella Cuviert, or Inoceramus mytiloides,
with the Melbourn Rock at its base.
These successive divisions are described as distributed in the
several counties and in the North of France.
Throughout the long series of Memoirs published by the Geolo-
gical Survey of Great Britain and Ireland, descriptive of the districts
already surveyed, there are frequent allusions to the economic
materials procured from the land, and to the relative conditions of
the soil and subsoil. About 1871 the Geological Survey made a
point of mapping the “Surface Drifts,” such as the gravels, brick-earth,
and boulder-clay, beginning with those of the Midland Counties,
so that the agriculturalists of several wide districts have since then
had the opportunity of recognizing and studying the nature and
origin of the surface soils in connexion with the notes and explana-
tions frequently given in the ‘ Memoirs.’ In fact, the Secretary of
the Board of Agriculture, cognizant of the advantages of geology to
the farmer, wishes to advance its publicity and causes copies of the
Memoirs to be distributed to scientific centres for recognition and
review.
A Treatise on Zoology. Kdited by E. Ray Lanxersrer, M.A., LL.D.,
F.R.S., &e.—Part I. Introduction and Protozoa. Second Fascicle.
1903. London: Adam and Charles Black.
Ir has been found necessary to publish Part I. of Prof. Lankester’s
‘ Treatise on Zoology’ in two fascicles, and of these the second
forms the subject of the present notice. The decision of the editor
not to delay the publication of this volume until the first was ready
is undoubtedly, both in the interests of the student and the authors
of the several sections, a wise one.
Anything like a complete account of the several contributions to
this fascicle would be impossible in the space at our disposal. Four
in number, they are the work of Messrs. Farmer, Lister, Minchin,
and Hickson, whose names are a sufficient guarantee that the quality
of the work is not only sound, but of the best that can be got.
Prof. Farmer contributes a section on Animal and Vegetable
Cells, wherein he traces the history of the cell from the epoch-
making discovery by Hooke in 1665 ‘ of the chambered structure of
160 Bibliographical Notices.
plants” to the latest revelations of the modern microscope. Wide
though this survey is, and admirable in its treatment, we yet feel
some surprise at the omission of any reference to the views of
Mr. Sedgwick on the subject of the cell-theory.
The section on the Foraminifera by Mr. J. J. Lister is a monu-
ment of thoroughness. Embracingall the results, of any consequence,
of the work of others in this field, he has added much that is new,
presenting his facts with great clearness and force. We have only
one small omission to notice, and that is the absence of Sherborn’s
‘ Bibliography of the Foraminifera’ and his ‘ Index to the Genera
and Species of the Foraminifera’ from the list of “ Literature
referred to.”
Scarcely less valuable is the section by Prof. Hickson on the
Infusoria (Corticata Heterokaryota). It is refreshing to remark in
reading this section, and also other sections of this treatise, a more
philosophical method of treatment than is to be found in any other
similar work.
But the bulk of this book is devoted to what may justly be called
the masterly treatise on the Sporozoa by Prof. E. A. Minchin.
Remembering the part that many of these lowly organisms play as
parasites and the ravages they commit, there can be no doubt but
that the decision to make this section as complete as possible will be
commended. To the medical man, as well as to the biologist, it will
prove a source of great help, inasmuch as the author’s account of
the life-history of the malaria parasite is the first which has
appeared in a general work on natural history in this country.
Besides this, however, there is much else in the section that is now,
for the first time, placed before the student in a readily accessible
form, and a very great deal that is the result of laborious research
on the part of the author himself.
Like the earlier parts, the tone of this volume is seriously dignified
and the matter of the very best of its kind possible. There is a
wealth of illustrations, all of which are excellent and many are
new. We await with impatience the appearance of the first
fascicle.
WE regret to announce the death of Dr. Wuittram Francis, for
many years one of the Editors of this Magazine, which took place
on the 19th January. A short notice will appear next month.
THE ANNALS
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]
No. 75. MARCH 1904.
XIX.—A Synopsis of the Suborders and Families of
Teleostean Fishes. By G. A. BOULENGER, F.RS.
For several years I have been endeavouring to improve the
classification of 'Teleostean Fishes, chiefly through a study of
their skeletons, of which a large series has been prepared in
the British Museum; and Dr. A. Smith Woodward has
recently published his views on the arrangement of the fossil
types of this order. The time has come to gather together
the information thus obtained. The synopsis here offered was
prepared two years ago for the fish-volume of the ‘ Cambridge
Natural History,’ but owing to circumstances over which I
have had no control its publication in that work is still further
delayed. Several important changes to my original scheme
have been made during this lapse of time, owing to the work
carried on in America by Drs. Gill, Jordan, and Starks, and
in this country by my young colleague Mr. ©. Tate Regan,
whose criticisms on many points I gratefully acknowledge.
I need hardly say that I regard this new arrangement of
an enormous and most difficult group, including close upon
12,000 species, as merely provisional, and I am fully aware
that not a few groupings are nothing but card castles, which
future investigations are likely to upset. But my aim has
been to build up on phylogenetic lines, and as such I sincerely
trust my attempt will be found a considerable improvement
on the previous systems and serve as a basis for criticism,
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 11
Teleostei.
162 Mr. G. A. Boulenger on the Suborders and
The arrangement here proposed has been used in the
‘ Zoological Record ’ for 1902, which has just appeared.
The precise definition of the order Teleostei, as compared
with the Holostean Ganoids, is a matter of some difficulty.
‘he most important character appears to be the presence of
an ossified supraoccipital bone. Remnants of primitive
characters, such as Ganoid scales, fulcra, rudiments of a
splenial bone, spiral valve to the intestine, multivalvular
bulbus arteriosus, are still found in some lower Teleosteans,
but no longer in that combination which characterizes the
preceding Order. Although Albula is exceptional among all
‘Teleosteans in having two transverse series of valves to the
bulbus arteriosus instead of one, no Ganoid has fewer than
three. The order Teleostei, thus defined, is divided into
thirteen suborders, the probable relations of which are
expressed in the following diagram :—
—XI. Opisthomi. XII. Plectognathi. XII. Pediculati.
IX. Anacanthini. X. Acanthopterygii. VIII. Percesoces.
| |
VII. Catosteomi. V. Haplomi. VI. Heteromi.
—IV. Apodes.
—III. Symbranchii.
I, Malacopterygii. II. Ostariophysi.
Ganoidei Holostei.
In the classification of Giinther, which has been generally
in use in this country for the last thirty-five years, the
Teleosts were divided into six principal groups, regarded as
of ordinal rank:—1. Acanthopterygi; 2. Acanthopterygii
Pharyngognathi; 8. Anacanthini; 4. Physostomi ; 5. Lopho-
branchii; 6. Plectognathi. Group 1 corresponds to Suborders
VI. (part.), VIL. (part.), VILE. (part.); X-, X1., and Same
of the present classification ; Group 2 to Suborder X. (part.) ;
Group 3 to Suborders IX. and X. (part.) ; Group 4 to Sub-
orders J, IL, IL., TV., V., V1. (Goart.),, and “VY Eagar) se
Families of Teleostean Fishes. 163
Group 5 to Suborder VII. (part.) ; and Group 6 to Sub-
order XIII.
Fuller definitions of the families, with an indication of the
principal genera contained in each, will be given in the forth-
coming seventh volume of the ‘ Cambridge Natural History.’
Suborder I. MALACOPTERYGII.
Air-bladder, if present, communicating with the digestive
tract by a duct. Opercle well developed. Pectoral arch
suspended from the skull ; mesocoracoid arch present. Fins
without spines, the ventrals abdominal, if present. Anterior
vertebre distinct, without Weberian ossicles.
This suborder, which corresponds to the Isospondyli and
Scyphophori of Cope and to a part of the Isospondyli of
A. 8. Woodward, embraces the most generalized of the
Teleosts, and is intimately connected with the Holostean
Ganoids by the fossil forms which are placed at the base of
the series of families. ‘The physostomous condition of the
air-bladder, the connexion of the pectoral arch with the skull,
the presence of a mesocoracoid arch, the backward position of
the many-rayed ventral fins, the normal condition of the ante-
rior vertebra, the absence of true spines to the fins, and the
separation of the supraoccipital bone from the frontals by the
parietals are primitive characters which occur combined in
some families of this suborder only. ‘The mesocoracoid arch
is retained by the Ostariophysi, which differ in the remarkably
modified condition of the auterior vertebra, but it disappears
in all other Teleosts, which gradually acquire a more forward
position of the ventral fins and a reduction in the number of
their rays, develop spines in the vertical fins, and lose the
communication of the air-bladder with the outside.
The Malacopterygii may be divided into twenty-one
families :—
I. Fins fringed with fulcra, or scales coated with ganoine; notochord
usually continuous through the vertebre (connecting forms
between Ganoids and Teleosts).
Vertebral centra not more than rings; fins with
fulera; scales rhombic, united by peg-and-
BOGE ARE 3 Soo oo oid ol ake tattle. «chs 1. Pholidophoride *.
Vertebral centra not more than rings; fins with
Hera Menles CYELOIM 7s, 22.25 6 ones. oe 2. Archeomenide fF.
Vertebral centra complete or with minute per-
foration; fins with fulera; scalescycloid .. 3. Oligopleuride *.
Vertebral centra nearly complete, but with per-
foration ; no fulcra; scales cycloid........ 4, Leptolepidide ¢.
+ This sign indicates that the family is represented by fossil forms ouly.
11*
164 Mr. G. A. Boulenger on the Suborders and
Il. Fins without fulera; scales without ganoine; vertebral centra
usually complete.
A. Supraoccipital separated from the frontals by the parietals.
1. Ventral fins with 10 to 16 rays.
Anintergular bone; parasphenoid narrow .... 5. Elopide.
No intergular bone; parasphenoid very broad.. 6, Adbudide.
2. Ventrals with not more than 7 rays.
a. Supratemporal very large, plate-like, covering the greater
part of the parietal bone.
Preemaxillary single, its posterior extremity free
from the maxillary; symplectic absent ;
basis cramil simple) i.e. eere cine © souls 7. Mormyride.
Preemaxillary paired, its posterior extremity
firmly attached to the maxillary; sym-
plectic present ; basis cranii double ...... 8. Hyodontide.
b. Supratemporal small; maxillary firmly attached to posterior
extremity of preemaxillary.
Preemaxillary paired; a large hole on each side
of the skull, between the postfrontal and the
squamosal; basis cranii double; suboper-
culumvabsents ribs Sessile 5.0m. eotehi et 9. Notopteride.
Premaxillary paired; basis cranii simple; sub-
operculum reduced; ribs inserted on para-
POPHYSEB./ i aie Gite Ciklvis elo nieleh teins 10. Osteoglosside.
Premaxillary single; basis cranii simple; sub-
operculum and interoperculum absent; ribs
inserted on parapophyses...... teas etacre UL. ehantedontiace,
c. Supratemporal small; maxillary movable; ribs sessile ; ven-
tral fins below the pectorals .... 12. Ctenothrisside t.
B. Supraoccipital in contact with frontals.
1. Interoperculum enormous; symplectic absent; basis ecranii
Simple; c0h nai eee ee ss 13. Phractolemide.
2. Interoperculum normal ; symplectic present; basis cranii
double.
a. Teeth in sockets; maxillary firmly attached to pre-
maxillary.
Symplectie exposed, fitting into a notch of the
Quatrabe cee mw reine oe erin eee .... 14, Saurodontide t.
Symplectic hidden between the quadrate and
the hyomandibular 2. .¢--. +e. ors s .. 15. Chirocentride.
6. Teeth not in sockets.
Postclavicle on outer side of clavicle ; no adipose
dorsal fin) 2 jo. cee ete eee 16. Clupeide.
Postclavicle on inner side of clavicle ; an adipose
Glorsall Min ictesnccesetersie siete aoa weeeee 17. Salmonide.
Postclavicle absent; no adipose dorsal fin...... 18. Alepocephalide.
3. Interoperculum normal; basis cranii simple,
Maxillary large, toothed; praecaudal vertebree
without well-marked parapophyses ; scales
cycloid or absent ; adipose dorsal fin present
OF SSEIE qereretorans meres center eran Cette ena
wo)
. Stomiatide.
Famities of Teleostean Fishes. 165
Mouth small, toothless; vertebras with strong
parapophyses; head and body covered with
Spa SCALERIN, 65/5: 4 stares Se Hiatus seelace Heer 20. Gonorhynchide.
Mouth small, toothless; no symplectic; head
und body naked 0.53.2... lee. Nahata beret Pir, 21. Cromeriide.
Suborder II. OSTARIOPHYSI.
Air-bladder, if well developed, communicating with the
digestive tract by a duct. Pectoral arch suspended from the
skull; mesocoracoid arch present. Fins without spines, or
dorsal and pectoral with a single spine formed by the co-ossifi-
cation of the segments of an articulated ray. The anterior
four vertebre strongly modified, often co-ossified and bearing
a chain of small bones (Weberian ossicles) connecting the
air-bladder with the ear.
This is one of the most natural groups of the class Pisces,
although its members are so diversified in outward appear-
ance as to have been widely separated in the systems of
older authors. It is to Sagemehl* that is due the credit of
having first grouped, under the above name, the Characines,
the Carps, the Catfishes, and the Gymnotids, the relations of
which had been realized to a certain extent by Cope. But it
was not until the homology throughout the group of the
ossicula auditus, first described by KE. H. Weber in 1820, had
been demonstrated by Sagemehl that the justification for the
course here followed appeared in its full strength, as such an
agreement in the structure of so complicated and specialized
an apparatus can only be the result of acommunity of descent
of the families which are pessessed of it. It is invariably
the anterior four vertebree that take part in the support of the
Weberian apparatus. ‘The first vertebra is much reduced ;
_ its upper arch is absent and replaced by the ossicles termed
claustrum and scaphium {, the former being perhaps nothing
but the modified neural arch, which fill in the space between
the exoccipital and the neural arch of the second vertebra;
the principal piece of the apparatus, the ér/pus, variable in
form, is related to the third vertebra, of which it is regarded
as a modified rib; a fibrous ligament extends from the ante-
rior extremity or the ¢trzpus to the scaphium, and in this
ligament is inserted the fourth piece, the ¢ntercalarium. The
various forms of this suborder also show a complete agree-
ment in the spinal nerves which pass through these ossicles.
* Morphol. Jahrb. x. 1885, p. 22. }
+ For the nomenclature of these ossicles, ¢f. Bridge and Haddon, Proc.
Roy. Soc. xlvi. 1889, p. 310.
166 Mr. G. A. Boulenger on the Suborders and
The parietal bones either separate the frontals from the
supraoccipital or are fused with the latter.
This suborder is divided into six families. The Characinids
are the most generalized, and the others are probably derived
from them in the manner expressed by the following
diagram :—
Loricariide. Aspredinide.
Cyprinide. Siluride. Gymnotide.
Characinide.
J. Parietal bones distinct from the supraoccipital ; symplectic present;
ribs mostly sessile, all or the greater number of the precaudal
vertebrae without parapophyses.
Mouth not protractile, usually toothed; pharyngeal
bones normal; body scaly ; an adipose dorsal fin
Often pPresenitin | dai ha tac aia'vee eeelerls aie eee: 1. Characinide.
Mouth not protractile, usually toothed; pharyngeal
bones normal; body eel-shaped, naked or scaly ;
vent under the head or on the throat .......... 2. Gymnotide.
Mouth usually more or less protractile, toothless ;
lower pharyngeal bones large, falciform; body
naked or scaly ; no adipose dorsal fin .......... 3. Cyprinide.
II. Parietal bones usually fused with the supraoccipital ; symplectic
absent ; body naked or with bony scutes ; mouth usually toothed,
with barbels; adipose dorsal fin often present.
Ribs attached to strong parapophyses; operculum well
ewe lOped ae ces wtas peeks eh cise ehaa © toe arora ai 4, Siluride.
Ribs sessile; parapophyses absent ; operculum more
or less developed; mouth inferior.............. 5. Loricariide,
Ribs sessile; strong parapophyses to the vertebre ;
operculumsabsenbie ait cneeiise eeniae eeeite sk 6. Aspredinide.
Suborder II]. SyMBRANCHII.
Eel-shaped fishes without paired fins, with the pectoral
arch free or suspended from the skull and with the anterior
vertebre distinct, without Weberian ossicles. Gill-openings
confluent into a single ventral slit. Air-bladder absent.
Families of Teleostean Fishes. 167
The structure of the skull conforms to that of typical
Malacopterygians. The premaxillary and maxillary are
both well developed, the latter placed behind the former, and
forming but a very small part of the oral border; the
symplectic is present; the parietals form a long sagittal
suture and separate the frontals from the supraoccipital. The
vertebrae are very numerous, the precaudals bearing very
strong parapophyses, to which short slender ribs are attached.
The skin is naked (Symbranchide) or covered with minute
scales (Amphipnoide), and the vertical fins are rudimentary,
reduced to mere dermal folds.
Like the Apodes, these fishes are no doubt derived from
some low type with abdominal ventral fins, but whether from
the Malacopterygii or the Haplomi we have as yet no data
from which to conclude,
Only two families :—
Post-temporal well developed, forked, attached to
EVESVASIEEIL EN ay ty Ge Se ce tae hee encom a aw SFr an loes sy « 1. Symbranchide.
Post-temporal absent, the shoulder-girdle free from
Poop setl leeds oghie «ale o.sl ore for Aboar eter reves 2. Amphipnoide.
Suboder IV. APODES.
Air-bladder, if present, communicating with the digestive
tract by a duct. Premaxillaries absent; the maxillaries, if
present, separated on the median line by the coalesced ethmoid
and vomer. Pectoral arch, if present, not connected with and
remote from the skull; mesocoracoid arch absent. Fins
without spines, the ventrals absent. Anterior vertebra
distinct, without Weberian ossicles.
The Apodes, or Hels, are elongate serpentiform fishes with
naked skin or with minute scales imbedded in the skin, the
opercular bones small and completely hidden under the
integument, narrow or minute gill-openings, the vertical fins,
it present, confluent behind or separated by the projecting
tip of the tail. ‘The pterygo-palatine arch is often reduced or
absent, and there is no distinct symplectic ; the supraoccipital
bone is small, separated from the trontals by the parietals,
which meet on the middle line. The vertebrae are very
numerous (up to 225) and the preecaudals bear strong para-
pophyses, to which short slender ribs may be attached ;
epineurals are sometimes present.
The five families into which this suborder is divided show
remarkable degrees of simplification in the structure of the
168 Mr. G. A. Boulenger on the Suborders and
skull, through reduction or loss of either the maxillary or the
pterygo-palatine arches.
Five families :—
Maxillaries present, separated on the median line
by the ethmo-vomer; _ palato- pterygoid
present, connected with the hyomandibular
and quadrate ; gill-clefts separate, opening
into the pharynx by wide slits; tongue
present ; vent far removed from the head.. 1. Anguilhide.
Distinguished from the preceding by the position
of the vent, which is close to, or at no great
distance from, the gill-openings .......... 2, Nemichthyide.
Maxillaries narrowly separated on the median
line, their extremity strongly attached by
ligament to the mandible ; pteryzo-palatine
arch absent; gill-openings externally con-
fluent into a single ventral slit............ 3. Synaphobranchide.
Maxillaries narrowly separated on the median
line, extremely elongate ; mouth enormous ;
pterygo-palatine arch absent; hyomandi-
bular arch slender and movably articulated
to the cranium ; branchial arches far behind
tHe GhUll oe wee ees eineues Mees 4, Saccopharyngide.
Maxillaries absent, replaced by the palato-
pterygoid, the mouth bordered by the latter
and the ethmo-vomer; palato-pterygoid
bone separated from hyomandibular arch ;
branchial openings into the pharynx narrow
TMG KO) ou AA Sirona linn aa bam 5. Murenide.
Suborder V. HAPLOMI.
Air-bladder, if present, communicating with the digestive
tract by a duct. Opercle well developed. Pectoral arch
suspended from the skull; no mesocoracoid arch. Fins
usually without, rarely with a few spines; ventrals abdo-
minal, if present. Anterior vertebre distinct, without
Weberian ossicles.
The absence of the mesocoracoid arch distinguishes the
Haplomi from the Malacopterygii, with which they are
united by various authors. ‘They lead to the Percesoces
through the Cyprinodontids, and to the Lower Acantho-
pterygians, such as the Berycids, through the Scopelids,
Stephanoberycids, and Percopsids, as is evidenced by the
structure of the mouth and the forward position in some of
the genera of the ventral fins, which, however, are never
attached to the pectoral girdle. Most of the forms which
are here included inhabit either fresh waters or the deep sea.
Families of Teleostean Fishes. 169
Fourteen families :—
I. Parietals separating the frontals from the supraoccipital; post-
temporal simple; przecaudal vertebrae with autogenous para-
pophyses.
Margin of the upper jaw formed by the pre-
maxillaries and the maxillaries ; basis cranii
simple ; no adipose dorsal fin ........... . 1, Galarude.
Margin of the upper jaw formed by the pre-
maxillaries only; basis cranii double;
adipose dorsal fin present................ 2. Haplochitonide.
II. Frontals in contact with the supraoccipital.
A. Precaudal vertebrae without parapophyses.
1, Margin of the upper jaw formed by the pramaxillaries and the
maxilaries.
Body without or with minute scales, usually
with rows of scutes; adipose dorsal fin
usually present: ...5.4...s<.. Sete Paso 3. Enchodontide t.
Body scaly ; post-temporal forked; no adipose
dorsal fin; ventrals with 6 toll rays .... 4, Esocide.
Body scaly; post-temporal incompletely ossified ;
pectoral tin without pterygials; no adipose
dorsal fin; ventrals with 3 rays only..... » 8. Dallide.
2. Maxillaries excluded from the oral border.
a, Adipose dorsal fin usually present; ventral fin with 7 to 10
rays.
Post-temporal forked; dorsal fin formed of arti-
SMC: TRY iar s ous aps; ceiars = Sate Basu s 4.078 6, Scopelide.
Post-temporal simple; dorsal fin very long,
formed of slender, non-articulated, simple or
DUM TAY Sie = fa) - Souss wot tee ... %, Alepidosauride.
6. No adipose dorsal fin; head and mouth enormous, dentition
feeble ; body naked ; ventral fins, if present, with 5 rays.
8. Cetomimide.
B. Preecaudal vertebrae with well-developed parapophyses ; maxil-
laries excluded from the oral border.
1. Dorsal and anal fins without spines; scales cycloid, or with
erect spines ; no adipose dorsal fin.
Mouth not protractile ; ventral fins far forward,
sR Ted Lhe Lea CVS raf er 28 tae acta, Orato eis. 5. 9. Chirothricide f.
Mouth not protractile ; ventral fins remote from
thespectorals, with Orrayss ose. .5s «aac 10. Knertide.
Mouth protractile ; ventral fins, if present, with
CO) P PAY Satan cc cai ft sete Deere, ails As as ll. Cyprinodontide.
Mouth scarcely protractile; ventral fins rudi-
mentary or absent; vent close to the gills.. 12. Amblyopside.
Mouth slightly protractile ; ventral fins with 5
OM GMAVGr Co. st i agh tape ae acc 13. Stephanoberycide.
2, Dorsal and anal fins with true spines; scales ctenoid; an adipose
dorsal fin ; ventral tins with 9rays.. 14. Percopside. q
170 Mr. G. A. Boulenger on the Suborders and
Suborder VI. HETEROMI.
Air-bladder without open duct. Opercle well developed ;
parietal bones separating the frontals from the supraoccipital.
Pectoral arch suspended from the supraoccipital or the epiotic,
the post-temporal small and simple or replaced by a ligament ;
no mesocoracoid. Ventral fins abdominal, if present.
The Halosauridz and Notacanthide are deep-sea fishes of
obscure affinities. In the abdominal position of the many-
rayed ventral fins and in the absence of the mesocoracoid arch
they agree with the Haplomi; but if, as the investigations of
Giinther lead us to believe *, there is really no open commu-
nication between the air-bladder and the digestive tract, they
should be removed from this physostomous suborder. The
two families have many characters in common, such as the
attachment and structure of the pectoral arch, which is devoid
of a postclavicle, the position of the pectoral fins high up the
sides, the strong parapophysis inserted very low down on the
centre of the vertebrze, the extent of the parietal bones, which
meet in a sagittal suture and separate the frontals from the
supraoccipital. The recent discovery of a third family, the
Lipogenyide, which in the structure of the dorsal fin is so
exactly intermediate between the two others, has lessened the
gap between the Lyomeri (Halosauride) and Heteromt
(Notacanthide) of Gill, which I propose to unite in a suborder
under the latter name. These fishes are no doubt derived
from forms in which a separate caudal fin existed; such a
type must have been near the Dercetide, as defined by A. 8.
Woodward, which may provisionally be placed here.
There is a fifth family which may be placed in this sub-
order, the Fierasferide, the structure of which has been
exquisitely described and figured by Emery. Hitherto
placed with or near the Ophidiide, they differ widely from
them, as well as from all other Acanthopterygians, in the
conformation of the skull, the supraoccipital being separated
* Vaillant was inclined to take a different view, but with considerable
diffidence, owing to his inability actually to trace an open duct. I believe
Giinther to be right on this point, as well as in his account of the suspen-
sion of the pectoral arch in Notacanthus, which I have been able to verify.
Besides, Mr. W. S. Rowntree, who has great experience in these matters,
has kindly examined at my request a well-preserved example of Halo-
sauropsis macrochir, and informs me that “ the air-bladder passes ante-
riorly into a tapering band of tissue which ends ina thread-like ligament
attached to the stomach near its posterior end and in the mid-dorsal line
—not to the cesophagus ; no trace of an open communication could be
found.”
Families of Teleostean Fishes. rie
from the frontals by the parietals, which form a long median
suture. ‘This is a feature which has oniy been observed in
fishes with abdominal ventral fins; and although the total
absence of these fins in Merasfer deprives us of an important
criteiion in deciding on its affinities, I am inclined to regard
this family as derived from an abdominal type. ‘The con-
formation of the pectoral arch has much in common with
that of the Halosaurs, and, notwithstanding the interpretation
that has been given to the bones at the back of the cranium
in the latter type, the same may be said in a general way of
the skull.
As pointed out by Emery, the very anterior position of the
vent in the Fierasferidee is directly related to the curious mode
of life of these fishes, and the analogous condition obtained in
various families, such as the Gymnarchide, Nemichthyice,
Amblyopside, and Aphredoderidz, shows it to be of relatively
small importance.
Five families :—
Ordinary scales small or wanting, but two or more
continuous series of enlarged scutes along each
side; mouth large, premaxillaries apparently
forming the greater part of the upper border of
the mouth, which is toothed; opercular appa-
ratus complete ; ; dorsal tin more or less extended,
without spines; anal short; caudal separate ;
ventrals with not less than 7 or 8 rays ........ 1. Dercetide ft.
Body covered with cycloid scales, the tail tapering to
a point, without caudal fin; head with scales ;
mouth moderate, bordered by the premaxillaries
and the maxillaries, both toothed; suborbitals
large ; preeopercle rudimentary ; dorsal fin short,
without spines; ventrals formed of 9 or 10 soft
rays; anal very long, without spines, extending
to the end of the tail ........cececcsseeeues 2. Halosauride.
Similar to the preceding, but with a toothless, round-
ish inferior mouth and with the short dorsal and
the leng anal formed partly of spines and partly
of soft rays; ventrals with 3 spines and 7 soft
BMS ses APNE Puro ote ti a Sees Wioataties fore aca a ee oe le > 3. Lipogenyide.
Body covered with cycloid scales, the tail tapering to
a point, without caudal tin ; head with scales;
mouth small, inferior, bordered by the preemax-
illaries only ; jaws toothed ; no suborbitals ; prie-
operculum small ; post-temporal replaced by
ligament; dorsal fin formed of a series of short
disconnected spines; anal very long, formed
partly of spines and partly of soft rays; ventrals
with 1 to 5 spines and 7 to 10 soft rays ...... 4, Notacanthide.
Body extremely attenuate, naked; no caudal fin;
“mouth small, inferior, bordered by the praemax-
172 Mr. G. A. Boulenger on the Suborders and
illaries; jaws toothed; no suborbitals; pre-
operculum well developed ; dorsal and anal very
long, formed of soft rays ; ventrals absent ; vent
immediately behind the gill-opening .......... 5. Fierasferide.
Suborder VII. CATOSTEOMI.
Air-bladder, if present, without open duct. Parietal bones,
if present, separated by the supraoccipital. Pectoral arch
suspended from the skull; no mesocoracoid arch; coracoid
usually very large, or produced posteriorly. Ventral fins, if
present, abdominal, or pelvis attached to the coracoid bones.
The mouth is bordered by the preemaxillaries, or by the
premaxillaries and a small portion of the maxillaries. Atr-
bladder present, except in the Solenostomide and Pegaside.
Following the suggestions of Kner and Steindachner and
Cope to their logical conclusion, A. 8. Woodward has united
the Lophobranchs of Cuvier with the Hemibranchs of Cope,
a course which seems fully justified, and has received further
support from the recent investigations of Swinnerton *, who
has proposed to unite the two groups under the new name of
Thoracostei. The structure of the Lophobranchs (Soleno-
stomide and Syngnathide) shows that these fishes are only
extremely specialized forms of the group of which the
Sticklebacks are the well-known type, and the character of
the “tufted” gills alone is surely not of sufficiently great
importance to warrant the retention of the Lophobranchii as
a division equivalent to the suborders adopted in the present
classification. Besides, as recently pointed out by A. Huot F,
there is no fundamental difference, only one of degree,
between the so-called tufted gill and the normal type; each
“tuft” corresponds to one branchial lamella, and at a certain
stage of development the disposition of the branchial lamella
is the same in a Syngnathus and an ordinary Teleostean. I
have recently attempted to show { that the Lampridide are
related to the Hemibranchil, although sufficiently distinct to
warrant the establishment of adivision, named Selenichthyes §.
The affinities of the Lamprididee are very doubtful. Lam-
pris has usually been placed with the Acanthopterygians, a
* Quart. Journ. Micr. Sci. xlv. 1902, p. 503.
+ Ann. Sci. Nat. (8) xiv. 1902, p. 197.
t Ann. & Mag. Nat. Hist. (7) x. 1902, p. 147.
§ E. C. Starks, in an important paper (P. U.S. Nat. Mus. xxv. 1902,
p- 619), has shown that the so-called “ infraclavicle” of sticklebacks and
allies does not exist as a distinct element. The definition of the Cato-
steomi as I had originally drawn it. up has accordingly been modified.
Families of Teleostean Fishes. La
view which is still upheld by Gill*. I now agree with this
high authority in regarding the bone which I took for an
infraclavicle as a much developed coracoid, and the bone
termed by me the coracoid as a pterygial. But it has also
been shown, by Starks, that such a thing as an infraclavicle
does not exist even in the stickleback, the bone so-called
being only a part of the coracoid; and as, in most of the
sticklebacks, the pelvic bones join the latter, the resemblance
between them and Zampris remains. As I have previously
pointed out, the absence of spines in the fins and the position
of the ventral fins, together with the great number of rays in
the latter, which is only met with in the lower Teleosteans,
are characters which necessitate the removal of Lampris from
the Acanthopterygians, and I cannot find a better place for
them than near the Gastrosteidie.
The whole question of the arrangement of the Physoclists
with abdominal ventrals (Catosteomi and Percesoces) is, L
feel, much in need of revision, and it may be found advisable
to break up this group into a greater number of suborders, in
which case the Selenichthyes would stand by themselves ;
the Hemibranchii and Lophobranchii would be united under
the former name, as proposed by Woodward, or under that of
Thoracostei (Swinnerton) or Phthinobranchii (Hay).
Eleven families :—
I, Preoperculum and symplectic distinct; branchial apparatus fully
developed, gills pectinate; mouth terminal, toothless; post-
temporal forked, free ; pelvic bones connected with scapular arch,
vertical fins with 15 to 17 rays; ribs long, sessile; fins without
spines, (SELENICHTHYES.).......... 1. Lampridide.
II. Preoperculum and symplectic distinct, latter much elongate ;
branchial apparatus more or less reduced, gills pectinated ; post-
temporal simple, immovable; mouth terminal. (HEMIBRANCHIL.)
A. Mouth toothed.
1. Pelvic bones close to or connected with scapular arch ; spinous
dorsal represented by isolated spines,
Snout conical or but slightly tubiform ; ventral
fins with one spine and one or two soft
rays; ribs slender, free ; anterior vertebrae
not enlarged.......... Shoee een Pee .. 2. Gastrostede.
Snout tubiform; ventral fins with one spine an
not enlarged..... TE CR aie Stem ie c lee 3. Aulorhynchide.
Snout tubiform; ribs slender, free; first ver-
fobruenlarceds. coma tistis css? «056 wsea.. 4. Protosyngnathide ft.
* Proc, U.S, Nat. Mus, xxvi. 1903, p. 915.
174 Mr. G. A. Boulenger on the Suborders and
2. Pelvic bones not connected with scapular arch; ventrals
without spine, with 5 or 6 rays; snout tubiform ; first ver-
tebra very elongate, formed by the fusion of several.
Isolated dorsal spines ; body scaly .......+. . 5, Aulostomatide.
No dorsal spines; body naked ...... sos has 6, Fistularude.
B. Mouth toothless; snout tubiform ; two short dorsal fins, the first
with a few spines; ventral fins with 3 to 5 rays; anterior ver-
tebree elongate.
Body covered with bony shields and small
Tongh sched: ascent ee 7. Centriscide.
Body completely cuirassed by bony shields,
which are fused with the endoskeleton .. 8. Amphisilde.
III. Preoperculum absent; symplectic much elongate ; branchial
apparatus more or less reduced ; gill-lamellz reduced in number
and enlarged, forming rounded lobes; post-temporal simple, im-
movably attached to the skull; mouth toothless, at the end of a
tubiform snout; body covered with bony plates. (LopHo-
BRANCHII.)
Two dorsal fins; ventral fins present, with 7
rays; gill-openings wide; exoskeleton of
large star-like plates ............++000- 9. Solenostomide.
A single dorsal fin; no ventral fins; gill-
openings very small; exoskeleton in the
ROL OL CANES |e. ,1n a Mois el ohe esas .... 10. Syngnathide.
IV. Preeoperculum and symplectic absent; gills pectinated; mouth
inferior, toothless ; body entirely covered with bony plates; ven-
tral fin with 2 or 3 rays. (fyPosTOMIDEs. )
ll. Pegaside.
Suborder VIII. PERCESOCES.
Air-bladder, if present, without open duct. Parietal bones
separated by the supraoccipital. Pectoral arch suspended
from the skull; no mesocoracoid arch. Ventral fins, if
present, abdominal, or at least with the pelvic bones not
solidly attached to the clavicular arch.
This group connects the Haplomi with the Acanthopterygil,
the Scombresocide being somewhat related to the Cyprino-
dontide *, whilst the Anabantide show distinct affinity to the
* Swinnerton (Quart. Journ. Micr. Sci. xlv, 1902, p. 554) has pointed
out that the skull of the Scombresoces belongs to what he terms the
Acrartete type (e. g. in which the attachment of the palatine cartilage or
its derivates is confined to the pre-ethmoid cornua), whilst the other
Percesoces examined by him, as well as the Cyprinodonts, are Disartete
(the attachment being at the par-ethmoid and pre-ethmoid cornua) ; but
the character is so indistinctly defined in some adult Cyprinodonts, that
I feel some diffidence in making use of this character for systematic
purposes in the present state of our knowledge.
Families of Teleostean Fishes, Ls
Osphromenide in the following suborder. Other families,
previously included among the Scombriform Acanthoptery-
gians, are placed here on the assumption that the loose
attachment of the pelvic bones to the clavicles is a primitive
character, and not the result of degeneration, such as occurs
in some cases among the Acanthopterygians. Although this
suborder is perhaps only an artificial association, it must be
borne in mind that, notwithstanding the very wide divergence
which exists between the first and last families, however
dissimilar their members appear to be at first sight, a gradual
passage may be traced connecting the most aberrant types.
Twelve families :—
I. Ventral fins, if present, inserted far behind the pectorals; no spines
to the fins.
Ribs attached to the extremity of much-developed
parapophyses ; lower pharyngeal bones com-
pletely united; pectoral fins inserted very
|e 6) | pee ae eae Grohe vecinittiay salt asdf 1, Scombresocide.
Ribs mostly sessile; lower pharyngeal bones
distinct ; pectoral fins nearer the ventral than
the dorsal line ...... SCobor chen ht “windy oo Ammodyide.
II. Ventral fins, if present, more or less approximated to the pectorals.
A. Two well-developed dorsal fins, the anterior small and formed,
at least in part, of spinous rays.
1. Ribs attached to strong parapophyses. 5
Pelvic bones free or connected with the clavicles
by hgament; pectoral finsinserted highup.. 3. Atherinide.
Pelvic bones suspended from the postclavicles ;
pectoral fins inserted very high up; teeth very
Lee ple OrimUseUh PH). anos one as gowns thes 4, Mugilide.
Pelvic bones suspended trom the postclavicles;
pectoral fins nearer the ventral than the
dorsal line, with detached lower rays ...... 5. Polynemide.
Pelvic bones connected with the clavicles by liga-
ment ; pectoral fins nearer the ventral than
the dorsal line; dentition powerful, cardi-
form ; scales minute or absent ............ 6. Chiasmodontide,
2. Anterior ribs sessile; pelvic bones not connected with the
scapular arch; pectoral fins nearer the ventral than the
Goce ln eee s iy acre hei ne ooo sresas, (. Sphyrenide,
B. Spinous dorsal, if present, connected with the soft.
1, Anterior vertebre without parapophyses; scales on head, if
present, small,
(Esophagus with lateral sacs which are beset with
papillae internally ; spinous dorsal long ;
scales rhomboidal, in oblique transverse
series; pelvic bones free ........505..5+5++ 8, Tetragonuride.
176 Mr. G. A. Boulenger on the Suborders and
(Esophagus with lateral sacs which are beset with
toothed papillze internally ; spinous dorsal,
if distinct, shorter than the soft dorsal;
scales moderate or small, cycloid, often
deciduous LE HELE eek ok ee eee ine 9. Stromateide.
No sacs in the cesophagus; fins without spines ;
scales very small orabsent . ot... .. ween « 10. Icosteide.
2. All or all but the two anterior vertebra with parapophyses ;
scales on head large ; a suprabranchial cavity.
No spines tothe fins'An I2 Ae. take ln ctr ccs ees 11. Ophiocephalide.
Strong spines to the dorsal, anal, and ventral fins. 12. Anabantide.
Suborder IX. ANACANTHINI.
Air-bladder without open duct. Parietal bones separated
by the supraoccipital ; prootic and exoccipital separated by
the enlarged opisthotic. Pectoral arch suspended from the
skull; no mesocoracoid arch. Ventral fins below or in front
of the pectorals, the pelvic bones posterior to the clavicular
symphysis and only loosely attached to it by ligament.
Fins without spines; caudal, if present, without expanded
hypural, perfectly symmetrical, and supported by the neural
and hemal spines of the posterior vertebra and by basal
bones similar to those supporting the dorsal and anal rays.
This type of caudal fin must be regarded, as I have pointed
out *, as secondary, the Gadide being no doubt derived from
fishes like the Macruride, in which the homocereal fin had
been lost. ‘The scapular foramen or fenestra is nearly always
between the scapular and coracoid bones, as in the Trachinidee
and several allied families, not in the coracoid, as in the
other Acanthopterygians. The first two vertebree have no
epipleurals.
Mr. C. Tate Regan +, who has recently given a good defi-
nition of the Anacanthini, divides them into three families,
which are here adopted :—
Ventral fins below the pectorals, with 7 to 12 rays ;
noyeaudal Mimo) A aha «chanel aengiaakeobolee tems eyo 1, Macruride,
Ventral fins jugular, with 1 to 9 rays; caudal
fin more or less distinct (diphycerca! or iso-
Cereal) .’..< aciemscyete See RoRnGNe kore oh eee te 2. Gadide. .
Ventral fins jugular, with 5 rays; no caudal fin;
pectoral pterygials in increased number (10) ;
scales as in the Anguillidze ..........00000% 3. Murenolendide.
* Ann. & Mag. Nat. Hist. (7) x. 1902, p. 295.
Tt Op. cit. xi, 1903, p. 460.
Families of Teleostean Fishes. 177
Suborder X. ACANTHOPTERYQGII.
Air-bladder usually without open duct. Opercle well deve-
loped ; supraoccipital in contact with the frontals. Pectoral
arch suspended from the skull; no mesocoracoid. Ventral
fins thoracic or jugular, the pelvic bones more or less firmly
attached to the clavicular arch. Gill-opening usually large ;
if small, in front of or above the base of the pectoral fin.
The character from which this suborder, the most com-
prehensive of the whole class, derives its name, viz. the
presence of non-articulated, more or less pungent rays In
the dorsal and anal fins, is by no means universal, exceptions
to the rule being numerous. The mouth is usually bordered
by the premaxillaries to the exclusion of the maxillaries, and
if these should, by exception, enter the oral edge, they are
always toothless. The ventral fins are sometimes inserted
at some distance behind the base of the pectorals (Haplo-
dactylide, Platycephalidz), in which case, however, this 1s
inerely due to the elongation of the pelvic bones, which are
solidly attached to the clavicular arch. The suborder is
broken up into 9 divisions, which follow in somewhat ar-
bitrary order, the natural affinities being opposed to a linear
arrangement,
I. No suborbital stay, or process extending from the suborbital bones
towards the preeoperculum; basis cranii double in the symmetrical
forms. Primary shoulder-girdle composed of a perforate scapula
and a coracoid; of the four or five pterygials, or basal bones ot
the pectoral fins, only one or two are in contact with the
coracoid ; ventral fins thoracic.
Rays of the caudal fin not strongly forked at
the base; hypural usually with a basal
spine or knob-like process on each side;
epipleural bones usually inserted on the
parapophyses or on the ribs; dorsal fin
usually with strong spines ; caudal peduncle
TArely, much-constricted gets. « yin’ sles I. PeERcIFORMES.
Rays of the caudal fin strongly forked at the
base, embracing a considerable portion of
the hypural, which always bears a_ basal
spine; epipleural bones usually inserted on
the centra or on the parapophyses, rarely
on the ribs; dorsal spines feeble or de-
tached; caudal peduncle much constricted ;
scales usually very small or absent........ If. ScoMBRIFORMES,
Rays of the caudal fin not strongly forked at the
base, no hypural spine, and ventral fins with
one spine and six to eight soft rays, or
Cranium asymimetrieal. ..... 12) ter, sineetls III, ZeEorwomst,
II. No suborbital stay; basis cranii double; scapula absent, the
pterygials inserted on the coracoid ; ventral fins thoracic.
1V. Kurrtirormes,
Ann. & Mag. N. list. Ser. 7. Vol. xiii. 12
178 Mr. G. A. Boulenger on the Suborders and
III. No suborbital stay; basis cranii simple; scapula and coracoid
more or less reduced, sometimes vestigial; pterygials large, only
one or two in contact with the coracoid ; ventral fins thoracic.
V. GoBIIFORMES.
IV. No suborbital stay ; basis cranii simple; a perforate scapula ;
three pterygials in contact with the coracoid ; ventral fins thoracic ;
a suctorial transversely laminated disk on the upper surface of the
hen soe ere ee Hig Slee g Ave develo «+e. VI. DiscocEPHALI.
V. A suborbital stay, the second suborbital bone being more or less
produced on the cheek or joining the preoperculum; ventral fins
ChOTHEIC Bee. Habre ORY tht Rare seek . VII. ScLeroparel.
VI. No suborbital stay; ventral fins usually jugular or mental, or, if
thoracic, structure of the pectoral arch differing from that ascribed
to the first five divisions of this Synopsis.
Pectoral fin with vertical or subvertical base ;
anal fin usually elongate, rarely small .... VIII. Jueurarrs,
Pectoral fin with horizontal or subhorizontal
base ; body exceedingly compressed ; dorsal
fin with all the rays simple; anal fin absent
or Wery Sara fs aah eu eee ee Tee et 7 Leake VNTOSsSOMm,
Division I, PERCIFORMES.
No bony stay for the preeoperculum. Basis cranii double.
Spinous dorsal usually well developed. None of the epi-
pleural bones attached to the centra of the vertebra in the
precaudal region. Pectoral arch with well-developed scapula
and coracoid, the former pierced by a foramen or fenestra ;
pterygials longer than broad, more or less regularly hour-
glass-shaped, 4 or 5 in number, one or two of which are in
contact with the coracoid. Ventral fins thoracic.
This large group, consisting chiefly of marine forms, has
members in all parts of the world, with the exception of the
Arctic and Antarctic regions, and was already represented by
numerous Berycid& and a few Serranide and Scorpidide in the
Upper Cretaceous. The division into families, capable of
rigid definition, is a task of considerable difficulty, and the
necessities of a linear arrangement result in the breaking
up of some natural sequences. Thus it appears highly
probable that the Scorpididx, themselves derived, together
with the Serranidee, from the Berycide, lead to the Carangide
in the division Scombriformes, whilst a nearly perfect
passage can be traced between the Acanthuride of this
division and the Balistidee among the Plectognaths.
Thirty-six families :—
JT. Gills four, a slit behind the fourth.
A. Two nostrils on each side.
1, Ventrals with one spine and 6 to 15 soft rays.
1, Berycide,
Families of Teleostean Fishes.
2. Ventrals with not more than 5 soft rays.
a. Lower pharyngeal bones not completely united, showing at
least a median suture.
a. Gill-membranes free from isthmus.
* Ventrals little if at all behind the pectorals. ‘
+ Third yertebra without transverse processes or with
sessile ribs.
¢t A more or less developed subocular shelf, or inner
lamina of the suborbitals supporting the eyeball,
sometimes reduced to a mere process of the second
suborbital.
§ Ribs inserted on the transverse processes, when
these are developed.
Body covered with very large bony scales ;
ventrals with a very strong spine and
2' or’ very short soft rays .............+
Dorsal very short, with few graduated, adnate
spipes; anal very lone. 62. .ccde aera.
Spinous dorsal usualiy well developed, soft
dorsal usually not much more developed
than the anal; palate usually toothed....
Dorsal and anal fins elongate and formed
mostly of articulated soft rays, the spines
distinct spines; body band-like ........
Teeth in the jaws fused to forma beak ......
Soft dorsal and anal much elongate ; a separate
BPMUOMS COLGAL Sirus erstd Stace tye ohsks 6 hasan men ass
Soft dorsal much longer than the anal; a
separate spinous dorsal
he site), 67: 6).6) 0. 0! ere 6 6) \e)ls\ 6.
16.
. Monocentride.
. Pempheride.
. Serranide.
2. Pseudochromidide,
. Cepolide.
. Hoplegnathide.
. Sillaginide.
§§ Ribs mostly sessile, behind
body deep; mouth moderately large and pro-
tractile.
Supratemporal forked, distinct from skull
Supratemporal completely ankylosed to the
skull; mouth very protractile ....
tt No subocular shelf.
25.
Scienide.
the parapophyses ;
Scorpidide.
Caproide.
§ Ribs mostly sessile, behind the parapophyses ;
anal spines 3 to 14.
Teeth conical; palate toothed; mouth freely
ARDRBEUTID UE DEE APs ld als obo Va a Soo roe ee
Teeth incisor-like ; fins densely scaled ......
Teeth conical; palate toothless..............
Maxillary very slender, mouth very protractile .
No entopterygoid ; mouth very protractile....
Centrarchide,
'yphoside.
Lobotide.
. Toxotide.
Nandide.
§§ Ribs inserted on the transverse processes when
these are developed; not more than 3 anal
spines.
Mouth not or but feebly protractile; palate
toothed; spinous dorsal usually Thrice
than the soft ; anal with 1 or 2 spines....
Mouth moderately protractile ; palate toothed ;
spinous dorsal not longer than the soft;
anal with 2 or 3 spines
Gente’ & oe Wy) poy Bl 6 va ee) 6
9. Pereide.
10, Aecranomatida,
124
180 Mr. G. A. Boulenger on the Suborders and
Mouth very protractile, preemaxillary with an
upward lateral process ; palate toothless.. 17. Gerride.
Mouth moderately protractile ; palate toothless ;
anal Jonger than soft dorsal; body scaly .. 18. Lactariide.
Mcuth moderately protractile; palate tooth-
less; anal much longer than soft dorsal ;
body naked sen eee > Lobes hye 19, Trichodontide.
tt Transverse processes developed on the third vertebra
and bearing the rib; palate usually toothless.
No subocular shelf; teeth small ........ w... 22. Pristipomatide.
A subocular shelf; teeth often either cutting
in front or molar-like on the sides ...... 23. Sparide.
A subocular shelf; teeth very small or absent;
a pair of barbels on the throat .......... 24. Mullide.
** Ventrals rather far behind the base of the pectorals ;
lower pectoral rays unbranched, often thickened ; no
subocular shelf,
Anal fin nearly as long as the soft dorsal .... 20. Latridide.
Anal fin much shorter than the soft dorsal.... 21. Haplodactylide.
8. Gill-membranes attached to the isthmus.
* Scales well developed ; vertebrae 24 or more.
A subocular shelf; mouth small; palate
tOULR CRS ARE tiny eel og teeta oe 27. Chetodontide.
No subocular shelf; mouth small; palate
LO OEHIEHS Meret cies. rste tet cet erence 28, Drepanide.
Subocular shelf more or less developed; a
superbranchial respiratory organ ........ 31. Osphromenide,
** Scales minute; mouth small; vertebrae 22 or 23,
Post-temporal not distinctly forked ; vertebrae
with strong transverse processes ; ventrals
with 1 spine and 2 to 5 soft rays ........ 29. Acanthuride.
Post-temporal forked ; vertebra without trans-
verse processes ; ventrals with 2 spines and
3 soft rays between them ......, Bat pats 30. Teuthidide.
b. Lower pharyngeals completely united into one bone, without
median sutures: SSF Nse eee 32. Embiotocide.
B. A single nostril on each side ; lower pharyngeal bones more or
less completely united, but with persistent suture; no sub-
ocular shelf; palate toothless ...... 33. Cichlide.
IT. Gills three and a half; lower pharyngeals completely united into
one bone, without median suture ; palate toothless.
A single nostril on each side; teeth conical or
incisor-like ; a subocular shelf .......... 34. Pomacentride,
Two nostrils on each side; anterior teeth
usually strong and canine-like; teeth on
pharyngeal bones conical or tubercular ;
no Silocularshelt crnrctcs) ose k eee 35, Lubride.
Two nostrils on each side; anterior teeth more
or less coalesced into a beak; teeth on
pharyngeal bones flat, tessellated; no
subocular shelf........ Pa ie ae ARS 536, Searide,
Families of Teleostean Fishes. 181
Division Il. ScOMBRIFORMES.
No bony stay for the preopercle. Spinous dorsal, if
distinct, formed of short or feeble, slender spines. Epi-
plenrals usually attached to the centra when ribs are sessile,
or to.the parapophyses of the vertebrae, rarely to the ribs.
Pectoral arch similar to that of the Perciformes, but ptery-
gials sometimes more abbreviated. Ventral fins thoracic.
Caudal fin, if well developed, with. very numerous rays
deeply forked at the base.
Although bound by natural ties, the series of families that
cluster round the mackerel offer so many modifications of
structure that it is almost impossible to draw up a diagnosis
differentiating every one of its members from the Perciformes,
with which they are closely connected, and from which they
hardly deserve to be separated. ven after removing many
genera which have been united with them by my _ pre-
decessors, and which will now be found scattered among
various groups of the system, no better definition of the
Scombriformes can be given than that the mackerel and
horse-mackerel are taken as the pattern-forms around which
more or less aberrant types are located, types yet not so
aberrant as to be traced back to these familiar forms through
a number of intermediate grades. As regards external
features, it may be stated that the dorsal and anal spines,
if present, are weak and slender, or, if strong, short and
detached, the caudal peduncle is constricted, and the caudal
fin, if well developed, is usually deeply forked and with the
forked bases of the very numerous rays much longer than
in most of the Perciformes, embracing at least a considerable
portion of the expanded ural bones, a character by which the
Chetodontide, Acanthuride, and several extinct types which
have been placed with the Carangidee are at once excluded.
Allare marine and many are pelagic and of very wide distri-
bution. No pretertiary members of this division, as here
defined, have yet been found.
Nine families :—
I, Premaxillaries more or less protractile, not beak-like ; scales small
or absent, sometimes with enlarged lateral scutes ; spinous dorsal
short or replaced by a series of isolated spines ; aval usually with
one or two spines detached from the rest of the fin.
Przecaudal vertebrae with transverse processes, behind
which the ribs are attached ...............5 1. Carangide.
Precaudal vertebree without well-developed para-
pophyses; ribs and epipleurals inserted close
fogether on the,contra |. siilia wns We. ake oe 2. Rhachicentride.
182 Mr. G. A. Boulenger on the Suborders and
II. Premaxillaries not protractile ; scales usually small or absent ; body
more or less elongate; dorsal fin elongate, single or divided,
without free spines ; no free anal spines.
A. Pseudobranchie present.
Vertebree without transverse processes; soft dorsal
fin longer than the spinous; pectoral fins high
up the sides..... fa, IEE REE Sots toe toe 3. Scombride.
Vertebree without transverse processes ; soft dorsal
fin shorter than the spinous, if the latter be
distinct ; pectoral fin low down the sides...... 4, Trichiuride.
Vertebree without transverse processes; snout pro-
duced into'a Spear) Weeki: ee meats aire ote 5. Histiophoride.
Vertebree with transverse processes bearing the
ribs; snout produced into a sword; no
WEMEEAIS,. 2 is.s ptocatespaeneness Je chisteeass nsipkedey «ia ieheate 6. Xiphude.
Vertebree without transverse processes; _ gill-
membranes attached to isthmus; dorsal and
anal fins formed of unarticulated, widely set
rays; dentition very feeble 7. Luvaride.
Pe ee
B. Pseudobranchizw absent; no well-developed transverse processes
to the preecaudal vertebre, the ribs and the epipleurals inserted
close together on the centra ; snout short and very deep.
8. Coryphenide.
WI. Premaxillaries not protractile, or, if slightly protractile, scales
large; dorsal and anal fins elongate, without distinct spinous
division; most of the precaudal vertebrae with strong hema-
pophyses, to which the mbs are attached.... 9. Bramede,
Division II]. ZEORHOMBI.
Aberrant, strongly compressed Perciformes, with very
short precaudal region, modified in the direction of the flat-
fishes, culminating in asymmetrical forms, and characterized
by the combination of an increased number (7 to 9) of
ventral rays, with absence of hypural spine (by which the
Berycice are excluded), or by asymmetry of the skull in
the forms in which the spine of the ventral fin has been lost.
Among the symmetrical forms, the existing Zeide agree
with the Berycide in having more than five soft rays to the
ventral fins, and are probably derived, together with the
Eocene Amphistiide, from some common ancestral group
still to be discovered in Cretaceous beds. These Zeide have
much in common with the Pleuronectide * and might be
regarded as forming part of the family out of which the
latter have sprung, were it not that they have lost the last
half-gill, Amphist‘um is probably more nearly related to
the Pleuronectida, which may have been directly derived
from the family of which it is as yet the only known
yepresentative T.
* Cf. Thilo, Zool. Anz, 1902, p. 305.
+ Cf, Boulenger, Ann. & Mag. Nat. Hist. (7) x. 1802, p, 296,
Tamilies of Teleostean Fishes. 183
This division embraces three families ouly :—
A spinous dorsal fin ; anal spines detached from
the soft portion; a ventral spine; gills three
and a half, three slits between them.......... 1, Zewde.
Dorsal and anal spines few, continuous with the soft
PAYS. 5 bi VEDITAMAPINEt: ee ce. sy nce es cles sree» 2. Amphistiide ft.
No spines; cranium twisted in front, with the two
orbits on one side; gills four, a slit behind the
Feat Aes 5 ade carats Pk sePs ta aig Nate's chad el aie 3. Pleuronectide.
Division IV. KURTIFORMES.
No bony stay for the preopercle. Dorsal spines feeble,
few. Scapula absent, the coracoid supporting four small
pterygials. Ventral fins thoracic.
A single family, Kurtide.
Division V. GOBIIFORMES.
No bony stay for the preoperculum. Basis cranii simple.
Spinous dorsal, if present, formed of few, flexible rays.
None of the epipleural bones attached to the centra of the
vertebre in the preecaudal region. Scapula and coracoid
more or less reduced or even vestigial; pterygials large,
4 or 5 in number, forming together a thin plate which is in
contact with or narrowly separated from the clavicle; one or
two of the pterygials in contact with the coracoid. Ventral
fins thoracic.
The Gobside, which alone constitute this division, are not
very remote from the Perciformes and may have evolved out
of a type not very different from the Percide.
Division VI. DISCOCEPHALI.
Highly aberrant Acanthopterygians with the anterior
dorsal fin modified into a suctorial, transversely laminated
oval disk on the head, the skull being very much flattened
and with simple basis cranii. The pectoral rays are inserted
on the small, perforate, scapula and on four hourglass-shaped
pterygials, three of which are in contact with the coracoid.
Ventral fins thoracic.
A single family, Echeneidide.
In spite of a superficial external resemblance to the genus
Elacate, the sucking-fish, as first observed by Gill, bear
certainly no affinity to that genus nor to other Scombri-
formes. They are probably derived from Perciformes, but
trom which family it is impossible to suggest.
184 Mr. G. A. Boulenger on the Suborders and
Division VII. SCLEROPAREI.
Second suborbital bone more or less produced towards or
ankylosed with the prxoperculum (“suborbital stay ’’) *.
Ventral fins thoracic.
The ‘‘Cheek-armoured Acanthopterygians,” ‘ Joues cuiras-
sées”’ of Cuvier, after the exclusion of the sticklebacks, form
a perfectly natural association, evidently derived from the
Serranide, with which the more generalized forms have
much in common. From the perch-like genus Sebastes a
continuous series can be traced towards the Triglida, espe-
cially through such forms as Apistus, Minous, and Chori-
dactylus, in which one or more of the lower pectoral rays are
detached from the rest of the fin. Through the Comephoride
the Scorpeenidee are connected with the Cottide, whilst the
latter merge insensibly into the still more aberrant Cyclo-
pteride. These conclusions, which are apparent enough
from a mere comparison of the external characters, become
fortitied by a study of the skeletons, The passage between
the various groups here accepted as families is so complete
that no serious objection could be raised to their union in
one great family with a number of minor divisions.
The character from which the Scleroparei derive their
name is subject to many modifications. The second sub-
orbital (the third, if the preeorbital be regarded as the first)
may be merely enlarged and prolonged over the cheek
towards the praoperculum (Sebastes, Anhoplopoma), or
firmly ankylosed to the latter (Scorpena, Platycephalus),
or form part of the externa] armature of the head (Zr7yla,
Dactylopterus). The structure of the base of the pectoral
fin appears to afford important characters for the definition
of the families, as first pointed out by Gill,
Kleven families :—
T. Head not completely cuirassed.
A. Ventral fins not widely separated; none of the pterygials in
coutact with the clavicle,
Two nostrils on each side; basis cranii double ;
gill-membranes free from isthmus ........ 1, Scorpenide.
A single nostril on each side; basis cranii double;
gill-membranes free from isthmus ........ 2, Hexagrammide.
Two nostrils on each side; basis cranii simple;
gill-membranes free or narrowly attached to
ISCAS. 5. sis Jeveete ets VCP OR HOS arvang Pha o's 3. Comephoride.
Two nostrils on each side; basis cranii simple ;
gill-opening narrow, above base of pectoral.. 4. Rhamphocottide.
* This character suffers one exception, to be found in Comephorus, a
degraded form otherwise closely related ta Cottocomephorus, 1 which
the skeleton is typical of the present division.
Families of Teleostcan Fishes. 185
B. Ventral fins, if present, not widely separated ; one or several of
the pterygials in contact with the clavicle.
Ventral fins distinct ; gill-clefts wide .......... 5. Cottide.
Ventral fins united into a sucking-disk; gill-
opening narrow, above base of pectoral .... 6. Cyclopteride.
C. Ventral fins widely separated; none of the pterygials in contact
with the clavicle.
Ventral fins behind base of pectorals ; preecaudal
vertebrae without transverse processes ...... 7. Platycephahde.
Ventral tins a little in front of base of pectorals;
precaudal vertebree with transverse pro-
COSSE Sarasa) os, aid oc + SORE ASTON at soet a #5 8. Hoplichthyide.
Il. Head completely cuirassed.
Ventral fins narrowly separated ; no pectoral ap-
pendages ; pterygials short and broad...... 9. Agonide.
Ventral fins widely separated ; 2 or 3 lowermost
rays of pectoral fin detached as feelers;
pterygials short and broad ..,.........85 10. Triglide.
Ventral fins narrowly separated; pectoral fin
divided into two portions; pterygials elon-
CEES eet ASS abe BMS de Ocbe Re ADEE 11. Dactylopteride.
Division VIII. JuGULARES,
“No bony stay for the preoperculum, Ventral fins jugular
or mental. Gill-openings in front of the pectoral fin, the
base of which is vertical or subvertical.
In a recently published note * I have alluded to the group
of physoclistous fishes for which I propose to revive the
old name Jugulares, pointing out that some of the forms
previously grouped together as Trachinide agree with the
Gadidee, not only in the jugular positioa of the ventral
fins, but also in the condition of the scapula and coracoid.
Mr. Regan f¢ has since been able to show that the Gadide
and Macruridz possess certain characters in common by which
they may be separated, not only from the other Jugulares,
but even from the Acanthopterygians, and, as mentioned
above (p. 176), the Miillerian suborder Anacanthini may be
maintained, after excluding the Pleuronectide. That the
Blenniidze are akin to Lycodes and allies has long been
admitted, and authors who have placed them in different
divisions of their systems have had to confess the difficulty
of referring certain genera to the one family rather than to
the other. The fact that Zycodes and many forms previously
associated with the Ophidiidz agree with the Macruridze and
Gadidze in the diphycercal vertebral column, and in the
* Ann. & Mag. Nat. Hist. (7) viii, 1901, p. 261.
+ Op, ett. xiv 1903, p. 459,
185 Mr. G. A. Boulenger on the Suborders and
absence of spines to the fins, is merely, it seems to me,
the result of degradation ; they probably form the terminal
group of a series in which the vertebral column was origin-
ally homocercal and fin-spines were present, as is the case in
most of the Blenniidee and Trachinidze and their near allies.
All these families may be assumed to have evolved in several
series, often on parallel lines, from some group closely related
to the Berycidee ; the resemblance which their terminal forms
bear to the Anacanthini is, as recognized by Regan, probably
to be ascribed to convergence, not to any close genetic
affinity.
Fifteen families :—
I. Pectoral rays attached to the scapula and to a series of pterygials,
of which only one or two are in contact with the scapula; ventral
fins jugular, with 1 spine and 4 or 5 soft rays; anterior dorsal
rays usually spinous or not articulated, often forming a detached
fin.
A. Epipleurals present.
1. Second suborbital produced inwards to support the eyeball.
Ventrals close together; scales very small, cycloid,
fonmine obliquetbandsa! 1) ia tone. Rim eee © 1. Trachinde.
Ventrals-widely separated 0. s.cceccessensns . 2 Percophide.
2. No subocular shelf.
Ventrals widely separated; two nostrils on each
SiOkewen : rere ot GAPE SAS OND OE aay or ae ipa nee deers 3. Leptoscopide.
Ventrals widely separated ; a single nostril on each
0 date Map ARE en Sek ALAS SiR nab than cantare ee dep isc 4, Notothenide.
Ventrals close together ; scales very small, forming
oblique bands; head partly covered with bony
UALES eo Somn'nire fel edn wie oe Br enn ae dae 5. Uranoscopide.
B. No epipleurals.
Post-temporal forked, articulated to the skull; soft
dorsal and anal much elongate ............., 6, Trichonotide,
Post-temporal closely adnate to the skull; soft
dorsal and anal short (with only 7 to lO rays).. 7. Calhonymide.
Post-temporal simple, articulated to the skull; soft
dorsal and anal short; a ventral sucker ..... . 8. Gobiesocide.
If. Pectoral rays all attached to the pterygials, of which two or three
are in contact with the scapula; ventral fins, if present, jugular
or mental, composed of | to 4 rays.
A. Ventrals jugular or absent.
Post-temporal distinctly forked; preecaudal ver-
tebre with transverse processes; some or all
of the dorsal rays spinous or not articulated ;
caudal fin usually distinct: «1s. ee © nee 9. Bienniede.
dorsal; caudal fin distinct ............ ..., 10. Batrachide.
Families of Teleostean Fishes. 187
Post-temporal distinctly forked; pracaudal ver-
tebre with hmal arches; dorsal rays all
Spinous 5 caudal fin distinct .......000+-ae0c ll. Pholidide.
Post-temporal distinctly forked; pracandal ver-
tebree with transverse processes; dorsal rays
all articulated, or a few of the posterior
spinous ; no distinct caudal ................ 12. Zoarcide,
Post-temporal forked, ankylosed to the skull; pre-
caudal vertebrae with transverse processes ; no
Epines’; no distinct caudal ey. .: ccs setae et 18. Congrogadide.
B. Ventrals mental (just behind the chin) ; no spines.
14, Ophidide.
III, Pectoral rays attached to an undivided cartilaginous plate repre-
senting the pterygials ; ventral fins jugular, reduced to a filament
formed of two adnate rays; fins without spines.
15, Podatelide.
Division 1X. Tn1osomt1.
Exceedingly compressed, more or less elongate, often
ribbon-like fishes of doubtful affinities, probably related to
the earlier Acanthopterygians, the ventral fins, when well
developed, comprising as many as 7 to 9 rays. Dorsal fin
extending from the head to the end of the tail, its rays
simple (separable into lateral halves), the anterior often
prolonged ; anal fin very short or absent. Pectoral fin with
horizontal, or nearly horizontal, base, the rays supported by
the scapula and by three short ‘pterygials, all three, or two
at least, of which are related to the coracoid. Jibs small
and slender, or absent. Post-temporal simple and solidly
attached to the skull. Scales minute or absent.
Deep-sea or pelagic fishes from the Atlantic and Mediter-
ranean and from the Pacific ; specimens are rare in collec-
tions and the life-histories are still very imperfectly known,
although it has been ascertained that great changes of form
take place with growth.
Only two families :—
Mouth very protractile; ventral fins more or less
developed, with 6 to 9 rays, or reduced to a
single long ray; no anal fin; vent about the
middle of the body; caudal rays, if present,
divided into two fascicles, the upper sometimes
much prolonged and directed upwards........ 1. Trachypteride.
Mouth moderately protractile ; ventrals very small,
if distinct, with 4 or 5 rays; body-cavity ex-
tending nearly the whole length of the much
elongate body, the vent very far back and fol-
lowed by a short anal fin; caudal fin small,
IRM APDCESC Wah 5 Spars. ei ath ote: v uaete nao viva ata eC 2, Lophotide.
188 Mr. G. A. Boulenger on the Suborders and
Suborder XI. OPISTHOMI.
Air-bladder without open duct. Opercle well developed,
hidden under the skin; supraoccipital in contact with the
frontals, separating the parietals. Pectoral arch suspended
from the vertebral column, far behind the skull; no meso-
coracoid ; no clavicle distinct from the cleithrum. Vertical
fins with spines. Ventral fins absent.
This division stands in the same relation to the Acantho-
pterygii as the Apodes to the Malacopterygil. The single
family, Mfastacembelide, inhabiting the fresh waters of
Southern Asia and Africa, is possibly derived from the
Blenniide.
Suborder XII. PEDICULATI.
Air-bladder without open duct. Opercle large, hidden
under the skin ; supraoccipital in contact with the frontals,
separating the parietals. Pectoral arch suspended from the
skull; no mesocoracoid. No ribs, no epipleurals. Ventral
fins jugular. Gill-opening reduced to a foramen situated in
or near the axil, more or less posterior to the base of the
pectoral. Body naked or covered with spines or bony
tubercles.
A small natural group, connected with the Acanthopterygil
Jugulares through the Batrachide, in which the elongate
pterygials of the pectoral fin foreshadow the kind of arm
(‘ pseudobrachium”’) which is more or less characteristic
of these highly aberrant fishes. As in the Batrachide, the
post-temporal is flat and ankylosed to the cranium, and the
suprascapula is much elongate. ‘The pterygials, two or
three in number, are separated from the small scapula and
coracoid by a broad ligament, the arm-like pectorals being
more or less distinctly geniculated and inserted far back
behind the cranium. The head is large, the basis cranii
simple. The gills are reduced to 2, 23, or 3. The spinous
dorsal, if present, consists of a few rays, which may be
modified into tentacles inserted on the head.
Five families :—
I. Gill-opening in or behind lower axil of pectoral; mouth large,
terminal or directed upwards.
Pectoral fin scarcely geniculated ; ventrals present . 1. Lophide.
Pectoral fin scarcely geniculated ; ventrals absent.. 2. Ceratude,
Pectoral fin strongly geniculated ; ventrals present. 3. Antennariide,
II, Gill-opening behind lower axil of pectoral ; mouth inferior ;
Ventrale-absent- tess tacts: fos ieeaeae tee 4. Gigantactouda,
Families of Teleostean Fishes. 189
IIT. Gill-opening above axil of pectoral; mouth rather small, sub-
terminal or inferior; pectoral fin strongly geniculated ; ventrals
present; spinous dorsal absent or reduced to a small tentacle
lodged in a cavity under the snout ........ 5. Malthide,
Suborder XIIT. PLECTOGNATHI.
Air-bladder without open duct. Opercular bones more or
less reduced; supraoccipital in contact with the frontals,
separating the parietals; maxillary and preemaxillary bones
often firmly united. Pectoral arch suspended from the skull;
no mesocoracoid. No ribs. Ventral fins thoracic and much
reduced if present; the pelvic bones, if present, more or less
completely co-ossitied. Gill-opening much reduced. Body
covered with more or less osseous scales, bony scutes, or
spines, or naked,
A highly aberrant group, closely connected with the
Acanthopterygii through the Acanthuride, as pointed out
long ago by Dareste *. The skeleton is often feebly ossified
and the vertebree much reduced in number, but the jaws,
although short, are very strong, usually with large sectorial
tecth which may be confluent into a beak ; the post-temporal
is short and simple, suturally united to the squamosal.
These fishes have usually been arranged in three divi-
sions: Sclerodermi, Ostracodermi, and Gymnodontes; but
Regan t, whose classification is here followed, has shown
that the latter include a type (TLriodon) which, in spite of
its beak-like teeth, is more nearly related to the Sclerodermi,
whilst the Ostracodermi have much more in common with
the latter than with the Gymnodontes. It therefore appears
best to admit only two divisions, the first with four, the
second with three families :—
I, ScteRopERMI. Supraclavicle vertical; pectoral arch of the Perci-
form type; all the vertebrze with a single neural spine.
A. Body covered with hard or spinous scales; epipleurals present ;
pelvis present.
Teeth separate; spinous dorsal present; ventrals
paired ; pelvis immovable’... 22... .. 222. .2. 1. Triacanthide.
A beak ; spinous dorsal and ventrals absent; pelvis
tad ? ° °
PILONGRDVECIM yori ei so" wot ns woe Scie spa ercje vos 2. Triodontide.
Teeth separate; spinous dorsal present; ventrals
absent or represented by a single short spine ;
jhe MiG ER Ea Pear ener sh eee . 3. Balistide.
B. Body encased in a carapace; no epipleurals; spinous dorsal,
pelvis, and ventrals absent ........... . 4. Ostraciontide.
* Ann. Sci. Nat., Zool. (3) xiv. 1850, p. 105, and C. R. Ac. Sci,
Isxiv. 1872, p..1527,
7 P. Z. 5. 1902, ni. p. 284,
190 Mr. C: T) Reganvon
Il. GymnoponTEs. Supraclavicle oblique or nearly horizontal; lower
three pterygials enlarged and immoyably united to the coraco-
scapular cartilage ; anterior vertebrae with bifid divergent neural
spines ; pelvis absent.
Beak with a median suture; interoperculum not
connected with suboperculum ; three gills;
caudal fin present ; body inflatable .......... 5. Tetrodontide.
3eak without median suture; interoperculum at-
tached posteriorly to suboperculum ; three gills;
caudal fin present; body inflatable .......... 6. Diodontide.
Beak without median suture; interoperculum at-
tached posteriorly to suboperculum ; four gills ;
caudal fin absent, the body non-inflatable, trun-
cate posteriorly, with the dorsal and anal fins
COMMWENE TSE RR IE boc ROR, es Oe Cie te 7. Molde.
XX.—On a Collection of Fishes made by Mr. John Graham
at Yunnan Tu. By C. Tate Reaan, B.A.
Tue British Museum has received from Mr. John Graham a
small collection of fishes from the large lake “ Sea of Tien,”
on the north shore of which the city of Yunnan Fuis situated.
This lake is at an altitude of about 6000 feet above the sea-
level, and its overflow runs northwards by the Pulu-shing to
the Yang-tse-kiang. Of thirteen species represented, eight
are described below as new to science. The complete list is
as follows :—
1. Cyprinus carpio, L.
The two specimens received both lack the anterior barbel *,
and should perhaps be referred to a distinct subspecies on this
account. Six examples in the British Museum Collection,
from the Southern Shan States, with large scales, 26-29 =,
may also be regarded as belonging to a geographical race or
subspecies,
2. Barbus Grahami, sp. n.
Depth of body 3} times in the total length, length of head
33 times. Snout nearly twice as long as the eye, the diameter
of which is 52 times in the length of head and 14 times in
the interorbital width. Mouth subterminal, maxillary not
extending to below the eye. ‘Iwo barbels on each side, the
anterior 3, the posterior nearly } the length of head.
* Some of the specimens figured in Reeve’s drawings of Chinese fishes
have apparently no anterior barbel,
Fishes from Yunnan Fu. 191
Se. 110 a 14 between lateral line and root of ventral; |. lat.
70. D. II 7, the third simple ray a strong spine, with finely
serrated posterior edges, the first branched ray the longest, §
the length of head; origin of dorsal equidistant from anterior
nostril and base of caudal. A. IIL 5. Pectoral not reaching
ventral. Caudal forked, the upper lobe slightly the longer,
a little less than the length of head. Caudal peduncle 1
times as long as deep. Brownish, with silvery reflections,
lighter below.
A single specimen, 170 mm. in total length.
3. Barbus yunnanensis, sp. n.
Depth of body 3? times in the total length, length of head
42 times. Snout 13 times as long as eye, the diameter of
which is 5 times in the length of head and 1? times in the
interorbital width. Mouth subterminal; maxillary not
extending to below the eye. ‘lwo barbels on each side, the
anterior }, the posterior ? the length of head. Sc. 46 @ 4
between lateral line and root of ventral. D. III 8, the third
simple ray a strong spine with serrated posterior edges, the
first branched ray the longest, # the length of head; origin
of dorsal equidistant from tip of snout and base of caudal.
A. II] 5. Pectoral not reaching ventral. Caudal forked,
the lobes as long as the head. Caudal peduncle 13 times as
long as deep. Brownish, with silvery reflections, lighter
below ; membrane of outer half of dorsal and anal blackish.
A single specimen, 210 mm. in total length.
4, Achilognathus barbatulus, Gthr.
5. Barilius polylepts, sp. n.
Depth of body 42 times in the total length, length of head
42 times. Snout nearly as long as the eye, the diameter of
which is 32 times in the length of-head and is nearly equal
to the interorbital width. Mouth small, oblique, the maxillary
not extending to below the eye; no barbels. Se. 70 22, 3
Bi?
between lateral line and root of ventral. D. III 7, its origin
a little behind that of the ventral and nearly equidistant from
tip of snout and base of caudal. A. IIL 13. Pectoral ex-
tending 3 of the distance from its base to the origin of ventral.
Caudal forked. Caudal peduncle twice as long as deep.
Brownish above, silvery on the sides and below.
A single specimen, 130 mm. in total length.
Allied to B. hatnanensis, Blgr., from which it is distin-
guished especially by the much smaller scales.
192 Mr. C. T. Regan on
6. Misgurnus anguillicaudatus, Cantor.
7. Nemachilus pleurotenia, sp. n.
Depth of body 5 times in the total length, length of head 4
times. Snout nearly as long as the postorbital part of head.
Diameter of eye 43 times in the length of head and nearly
equal to the interorbital width. Nostrils well separated, the
anterior tubular. Rostral barbels shorter than the one at
the angle of the mouth, which is 4 the length of head.
Scales minute ; thorax naked; lateral line present anteriorly,
disappearing before origin of dorsal. D. III 8, its origin
equidistant from anterior nostril and base of caudal, above or
slightly in advance of the origin of ventral. <A. III 5.
Pectoral extending 2 of the distance from its base to origin of
ventral. Ventral with 9 rays. Caudal bilobed. Caudal
peduncle 1J-14 times as Jong as deep. Back with some
dark spots or markings; a blackish longitudinal stripe along
the middle of the side; fins immaculate.
Two specimens, 46 and 51 mm. in total length.
8. Nemachilus nigromaculatus, sp. n.
Depth of body 4-44 times in the total length, length of
head 32 times. Snout shorter than the postorbital part of
head. Diameter of eye 43-5} times in the length of head,
interorbital width 8-34 times. Nostrils well separated, the
anterior tubular. Rostral barbels shorter than the one at the
angle of the mouth, which is less than 4 the length of head.
Seales very small, not imbricated; thorax and abdomen
naked ; lateral line absent. D. III 8, its origin equidistant
from middle of eye and base of caudal, a little in advance of
the origin of ventral. A. III 5. Pectoral extending 3-2 of
the distance from its base to origin of ventral. Ventral with
8 rays. Caudal truncate. Caudal peduncle as deep as or
deeper than long. Back and sides spotted or marbled with
blackish ; fins immaculate.
‘wo specimens, 61 and 77 mm. in total length.
9. Silurus mento, sp. n.
Depth of body 53-5} times in the total length, length of
head 4-43 times. Breadth of head 14-12 times in its length,
diameter of eye 74-94 times, interorbital width 3-34 times,
Jength of snout 32-4 times. Lower jaw projecting, the
mouth superior ; vomerine teeth in two separate patches; 4
barbels, the maxillary ones extending to the base of pectoral
Fishes from Yunnan Fu. 193
or beyond, the mental ones nearly ? aslong. LD. 4, its distance
from the tip of snout 4 its distance from the caudal. A. 71-
73, continued on to the caudal. P.112, the spine stout,
anteriorly somewhat roughened or slightly serrated, poste-
riorly with a series of 6-9 fairly strong teeth, its length a
little more than 4 that of the soft part of the fin, which
extends nearly to the origin of ventral. Ventrals with 10
rays, originating just in front of the vent and extending to
the third or fourth ray of anal. Caudal truncate rounded.
Greyish, clouded with blackish.
Two specimens, 115 and 215 mm. in total length.
10. Liobagrus nigricauda, sp. n.
Depth of body about 6 times in the total length, length of
head 32-3? times. Breadth of head 14-1} times in its
length, interocular width 23-3 times, length of snout about
34 times. Hyes very small. Jaws equal anteriorly ; mouth
wide. Post-mental barbel the longest, extending to base of
pectoral or a little beyond. JD. I 5, the spine concealed in a
fold of skin which also extends over the soft rays, about #
the length of head; adipose fin low, originating above or a
little in advance of the anal and extending on to the pro-
current rays of the caudal. A.15. P.17, the spine concealed
like that of the dorsal, a little more than } the length of the
fin, which is rounded and nearly equal in length to 2 the
length of head, extending 3 the distance from its base to the
origin of ventral. V.6. Caudalrounded. Greyish, spotted
or marbled with darker; dorsal and pectoral in great part
blackish ; ventrals and anal with or without blackish spots ;
caudal, in the smaller specimen, with a large median blackish
blotch confluent with a semioval blackish basal band, in the
larger specimen almost entirely blackish except for two small
light areas on the upper and lower margins respectively,
‘lwo specimens, 64 and 96 mm. in total length.
The genus Liobagrus, established in 1878 by Hilgendorf
for L. Reinit from Southern Japan, is allied to Akysis and
Acrochordonichthys, but is distinguished by the truncate or
rounded caudal and by the wide gill-openings, which are not
1estricted from above, whilst the gill-membranes are entirely
separate from each other and from the isthmus. Amblyceps
marginatus, Gthr. (Pratt’s ‘Snows of Thibet,’ Appendix,
p. 245, pl. 11. fig. A, 1892), is another species of this genus,
differing from the one described above in the coloration,
projecting lower jaw, longer barbels, and truncate caudal.
Amblyceps is distinguished from Liobagrus by the nostrils,
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 13
194 Mr. W. L. Distant on Capsidee
which are close together instead of well separated, and by
the forked caudal. In Liobagrus, as in Akysis and Acro-
chordonichthys, and also in Amblyceps, the air-bladder is
reduced to two small lateral portions enclosed in bone.
11. Macrones medianalis, sp. n.
Depth of body 53-54 times in the total length, length of
head 34-42 times. Diameter of eye 5-63 times in the length
of head, interorbital width 32 times, length of snout 33 times. -
Nasal barbel extending beyond posterior border of eye,
maxillary barbel to base of pectoral or beyond, post-mental
barbel to the edge of the gill-membrane at a point directly
posterior to its origin or a little beyond. Upper jaw slightly
the longer; width of mouth 34 the length of head. Upper
surface of head covered by skin; supraoccipital process more
than twice as long as broad, its length } that of the head;
basal bone of the anterior dorsal ray hidden beneath the
skin, separated by a short interspace from, or in contact with
the supraoccipital process. D. 17, the spine smooth, equal
to 3-3 the length of head; length of adipose fin equal to its
distance from the base of middle rays of caudal. A. 17-18.
P. I 7, the spine with a series of 5-8 teeth posteriorly, equal
in length to that of the dorsal. V. 6. Caudal bilobed.
Caudal peduncle twice as long as deep. Greyish, with a
few large dark spots or blotches.
Three specimens, 65-128 mm. in total length.
Although with less than 20 anal rays, the relations of this
species are with the section Pseudobagrus.
12. Monopterus javanensis, Lacep.
13. Ophiocephalus argus, Cant.
XXI.—Rhynchotal Notes—XXI. By W. L. Disranr.
HETEROPTERA.
Fam. Capside. (Part II.)
Tus paper concludes the examination of the Capside
contained in the British Museum, including Walker’s types ;
an the British Museum and elsewhere. 195
of some of these the condition is so imperfect as to make
their generic identification a matter of no little difficulty,
but they will be all found in the “summarized disposition ”
here appended.
Division MIRARIA.
NYMANNUS, gen. nov.
Elongately subovate; head as long as pronotum, sub-
conical, narrowed anteriorly, with a narrow central linear
suleation; eyes of moderate size, almost touching the
anterior margin of the pronotum; antennee about as long
as the body, first joint strongly incrassated, narrowed at
base, about as long as head, second joint slender, about
twice as long as first and almost equal in length to re-
maining joints together; rostrum almost reaching the
posterior coxee; pronotum nearly twice as broad posteriorly
as anteriorly, very faintly transversely impressed on anterior
area, posterior margin truncate, oblique beyond the scutellar
angles, mesonotum exposed ; scutellum subtriangular ; hem-
elytra a little convexly ampliated, cuneus longer than broad,
membrane short; posterior femora incrassated, posterior
tibia finely setose; first joint of posterior tarsi as long as
second and third joints together.
Nymannus typicus, sp. n.
Pale reddish-testaceous, basal lateral areas of corium
stramineous, clavus somewhat piceous; antenne with the
basal joint castaneous, second joint pale ochraceous, re-
maining joints fuscous; femora castaneous; tibize pale ochra-
ceous; tarsi, excluding base, fuscous; membrane dark
fuscous; body above finely shortly pilose ; narrow central
sulcation to head appearing as a fuscous line; basal angles
to scutellum linearly foveate and fuscous.
Long. 6 mm.
Hab. Cape Colony: Grahamstown (Albany and Brit.
Muss.).
Genus MEGACZLUM *.
Megacelum, Fieb. Wien. ent. Monats. Bd. ii. p. 305. n. 21 (1858).
Creontiades, Dist. Biol. Centr.-Amer., Rhynch. i. p. 237 (1883).
* I have here substituted the generic term Megacelum for Creontiades
(ante, p. 105). I had already sank as a synonym the proposed genus
13*
196 Mr. W. L. Distant on Capsidee
Pantiliodes, Nouath. Ann, Soc. Ent. Fr. 1893, p. 15.
Umslopogas, Kirk. Tr. Ent. Soc. 1902, p. 254.
Kangra, Wirk. Tr. Ent. Soc. 1902, p. 257.
Megacelum transvaalensis, sp. n.
Pale luteous; apex of head, eyes, subanterior and sub-
posterior transverse fascia to pronotum, broken at centres
and sometimes united along lateral margins, inner and outer
margins of clavus, an elongate spot on posterior disk of
corium which is angulated and connected with the mem-
branal margin, membrane, basal joint of antenne (remaining
joints mutilated), extreme apices of tibize, and the apices of
tarsi black; abdomen beneath with central and_ sublateral
fuscous fasciz; apices of femora and bases of tibia testa-
ceous ; pronotum finely transversely granulate; scutellum
shining, almost glabrous; hemelytra finely and obscurely
punctate; posterior tarsi mutilated.
Long. 6 mm.
Hab. Transvaal: Zoutpansberg (Junod, Brit. Maus.);
Pretoria (Distant).
Megacelum nigroquadristriatus.
Umslopogas nigroquadristriatus, Kirk, Trans. Ent. Soe. 1902, p. 254,
pl. v. fig. 11.
Head, pronotum, and scutellum pale shining greenish
yellow, pronotum usually more greenish; a central longi-
tudinal fascia to head, four longitudinal fascize to pronotum
(two central and one at each lateral margin, and sometimes
more or less fused anteriorly), and two basal spots and lateral
margins of scutellum, black; antenne fuscous; hemelytra
pale opaque greenish yellew, the clavus, inner area, and a
longitudinal apical spot to corium fuscous; membrane pale
fuscous ; body beneath and legs pale dull ochraceous, legs
speckled with fuscous, apices of tarsi piceous ; a narrow
sublateral fascia and sometimes apical segment to abdomen
piceous ; rostrum reaching posterior coxe; second joint of
Kangra, and since then have seen the species on which Umslopogas is
founded. It now becomes clear that to keep these genera distinct the
only reliable character is the proportional length of the joints in the
posterior tarsi (frequently mutilated in specimens received) ; and as this
seems to be but a sectional character of a large and well-marked genus,
I haye thought it best to now include all under Megacelum.
in the British Museum and elsewhere. 197
antennze about twice the length of first; corium finely
pilose.
Long. 7mm,
flab. Natal: Howick (Cregoe, Brit. Mus.). Transvaal:
Pretoria (Distant) ; Johannesburg (Ross).
The British Museum possesses a long series of this species
from Howick, Natal, whence Kirkaldy’s type is recorded,
and I have also a considerable number of specimens from
the Transvaal. They are all moderately uniform in markings
and coloration, and the figure given by Kirkaldy appears
to be much too highly coloured.
I found this the most abundant species in the Transvaal,
frequenting grasses, and readily obtained by sweeping.
Division CYLAPARIA,
CHAMUS, gen. nov.
Elongately subovate; head broad, anteriorly broadly
channelled, with three long, frontal, slightly upwardly curved
spines, one central and one before base of each antenna, two
discal callosities on posterior area; eyes prominent, inserted
near base of antenne, which are very robust and longly and
strongly pilose, first joint very strongly incrassate, moderately
petiolate at base, second joint almost twice as long as first,
third much shorter than second, twice as long as fourth;
rostrum reaching the anterlor coxe; pronotum with the
posterior margin about three times broader than anterior,
constricted before middle, the anterior area with two obscure
callosities ; scutellum in typical specimen destroyed by pin;
lateral margins of corium sinuate and ampliate posteriorly ;
cuneus somewhat large, a little longer than broad ; membrane
with a single elongate quadrangular cell; legs moderately
short, strongly and longly pilose; posterior legs mutilated ;
pronotum, corium, and cuneus somewhat thickly minutely
tuberculate, lateral margins longly and strongly pilose.
Chamus Wealet, sp. n.
Reddish testaceous ; second and third joints of antennsx,
extreme lateral margins of corium, rostrum, body beneath,
and legs stramineous ; pronotum and corium with numerous
small sanguineous tuberculations; cuneus and membrane
pale dull ochraceous, the first with the small tuberculations
198 Mr. W. L. Distant on Capsidee
sanguineous near inner angle, the membranal venation also
sanguineous; lateral margins of body beneath sanguineous.
Long. 64 mm.
Hab. Cape Colony (Mansell Weale).
Division ?
ARCULANUS, gen. nov.
Subelongate; head broad, subglobose, shortly obtusely
conically produced in front of eyes, a little narrowed pos-
teriorly and anteriorly ; eyes of moderate size, situate at about
centre of lateral margins; antenne moderately robust, very
finely pilose, first joint distinctly thickened from beyond base
and very slightly longer than head, second more than twice
as long as first, third much shorter than second, more than
half as long again as fourth; rostrum short, robust, about
reaching the anterior coxe; pronotum somewhat long, with
a broad anterior collar, narrowed anteriorly, strongly con-
stricted before middle, where there are two strong subconical
tuberculations, posterior area convexly tumid, foveate near
lateral angles, which thus appear subprominent, posterior
margin almost five times as broad as anterior margin ;
scutellum subtriangular, its lateral margins very slightly
convex ; corium somewhat long, its lateral margins a little
sinuate ; cuneus longer than broad and passing abdominal
apex ; membrane with a single elongate quadrangular cell ;
legs moderately short, femora a little thickened.’
A genus which may be placed near D)isphinctus.
Arculanus Marshalli, sp. n.
Pale sanguineous ; anterior margin of head, tuberculations
and lateral margins to pronotum, scutellum, outer claval area
to corium, basal area of cuneus, sternum, cox, rostrum,
bases of femora, tibia (excluding bases), and the tarsi more
or less pale ochraceous ; above shining, finely and obscurely
pilose; outer margin of clavus, inner margin of cuneus, and
two longitudinal discal lines on apical half of membrane
fuscous ; membrane pale bronzy, the venation sanguineous.
Long. 73 mm.
Hab. Mashonaland: Umfili River (G. A. K. Marshall).
in the British Museum and elsewhere. 199
Division PHYTOCORARIA,
Genus PARACALOCORIS.
Paracalocoris Barretti, sp. n.
Purplish brown ; head, antenne (excluding basal joint),
Jateral margins and a broad central fascia (attenuated
posteriorly) to pronotum, basal angles of scutellum, a very
small marginal spot near apex of corium, a marginal spot to
cuneus, body beneath, rostrum, and legs pale ochraceous ;
apices of second and third joints of antenne and apices of
tibia purplish red; pronotum with two discal black spots;
first joint of antennze incrassate and pilose, second joint
distinctly incrassate towards apex, about half as long again
as first; pronotum transversely rugulose; membrane very
pale fuscous with the veins darker.
Long. 53 mm.
Hab, Cape Colony: King William’s Town (Miss Barrett,
Brit. Mus.).
Division CAPSARIA.
Genus Lyaus.
Lygus Schonlandt, sp. n.
Ochraceous ; hemelytra somewhat longly pilose; apex of
second joint of antenne black (remaining joints mutilated) ;
basal area of pronotum, two central longitudinal fascie to
scutellum, inner area and two lateral spots (one before middle,
the other at apex) to corium, and a spot at apex of cuneus
piceous; basal and inner margins of cuneus generally
distinctly narrowly sanguineous; membrane fuscous with
paler mottlings; body beneath and legs pale ochraceous ;
mesosternum, a lateral spot to metasternum, base of posterior
tibie, and apices of tarsi black ; apical halves of posterior
femora castaneous with broad fuscous annulations; rostrum
reaching the intermediate coxe; pronotum finely and ob-
scurely punctate; first joint of antenne slightly thickened,
second joint a little more than twice the length of first.
Long. 4 to 44 mm.
Hab. Cape Colony: Grahamstown (Albany and Brit.
Muss.). Natal: Durban (Marshall).
£00 Mr. W. L. Distant on Capside
Genus Horctas.
Floreias Signorett.
Capsus Signoreti, Stal, Free. Fug. Resa, Hem. p. 257 (1859).
Capsus cinctipes, Walk. Cat. Het. vi. p. 109. n. 247 (1878).
Resthenia cinctipes, Atkins, Cat. Capside, p. 57 (1890).
Tlorcias obumbratus.
Capsus obumbratus, Walk. Cat. Het. vi. p. 111. n. 251 (1873).
Resthenia obumbratus, Atkins. Cat. Capsidee, p. 60 (1890).
Horcias? squalidus.
Capsus squalidus, Walk. Cat. Het. vi. p. 110. n. 249 (1873).
Resthenia squalidus, Atkins. Cat. Capside, p. 61 (1890).
A single specimen represents the type, in bad condition
and imperfectly described. The “ piceous band on the hind
border ” of the pronotum does not extend on each side beyond
the basal angles of the scutellum ; the corium is piceous
red, with a broad sublateral stramineous fascia; cuneus
carmine-red,
Lorcias lacteiclavus, sp. n.
Black ; pronotum (excluding basal margin), prosternum,
rostrum, segmental incisures, and legs pale ochraceous ;
clavus, margins of mesosternum, and three narrow marginal
lines to abdomen lacteous white; antennze black, annulation
io first joint, base of second, and third (excluding apex)
lacteous; posterior femora with a small lacteous spot on
upper surface near apex, posterior tibiae with two lacteous
annulations; membrane pale fuscous; shining, glabrous,
scutellum distinctly tumid; head elongately subconical.
Long. 5 mm.
Hab, Ecuador: Cachabé (Rosenberg, Brit. Mus.).
Horcias albiventris, sp. ne
Black ; head and pronotum (excluding basal margin) pale
ochraceous; head beneath, sternum, coxee, and abdomen
lacteous white ; intermediate legs ochraceous, tibize with a
broad, subapical, lacteous annulation, tarsi black ; anterior
and posterior legs mutilated ; apical joint of antenna lacteous ;
membrane pale fuscous; apex of head piceous; scutellum
distinctly tumid; body above shining, glabrous.
Long. 6 mm.
Hab. Ecuador: Chimbo (Rosenberg, Brit. Mus.).
Floreias signatus, sp. n.
Black ; head, pronotum, scutellum, a sublateral streak and
in the British Afuseum and elsewhere. 201
apical angle to corium, base and apex of cuneus, body beneath,
and legs ochraceous ; a central, discal, longitudinal spot and
Jateral angles of pronotum, lateral margins of abdomen beneath,
spots to tibiae, and the tarsi (excluding base) black; apical
halves of femora testaceous, speckled with black ; basal joint of
antennee (excluding apex), central annulation to second joint,
and base of third joint ochraceous; membrane pale fuscous,
with a lacteous spot near margin of cuneus; scutellum not
prominently tumid; body above shining, glabrous.
Long. 5 mm.
Hab. Colombia: Cali (Brit. Mus.).
Genus CYPHODEMA.
Cyphodema? Junodt, sp. n.
Head ochraceous, eyes and antenne black ; pronotum
ochraceous, somewhat coarsely punctate, with a very large
transverse, subbasal, black spot, which is angulately sinuate
anteriorly ; scutellum pale stramineous, with a central longi-
tudinal ochraceous fascia; corium and clavus black, the first
with a large central, marginal, pale stramineous spot ; inner
and apical margins of clavus, extreme lateral margin and apex
of corium and the cuneus dark ochraceous ; membrane fuscous,
black at basal angle; body beneath black, legs ochraceous,
bases of femora and apices of tibie black; hemelytra very
finely and obscurely pilose; second joint of antennee about
three times the length of first ; eyes large and transverse.
Long. 45 mm.
Hab. ‘Transvaal: Zoutpansberg (Junod, Brit. Mus.).
A single specimen, agreeing generally with the characters
and appearance of the genus Cyphodema.
Genus CAMPTOBROCUIS.
Camptobrochis Esau, sp. n.
Shining black, somewhat longly greyishly pilose; head
opaque, piceous, with a large testaceous spot at inner margin
of each eye; anterior and posterior margins of pronotum, a
broad central fascia to scutellum (not reaching base), corium
(excluding inner area and a submarginal punctate line), body
beneath, antennx, rostrum, and legs pale dull ochraceous ;
basal joint of antenne, apical halves of posterior femora, and
bases of posterior tibiee dull testaceous ; extreme base of first
joint and apices of second and third joints of antenne and
apices of the tarsi piccous ; antenn finely pilose, first and
second joints moderately thickened, second a little more than
twice as long as first ; pronotum distinctly punctate, scutellum
202 Mr. W. L. Distant on Capsidee
and corium a little more finely and obscurely punctate ; cuneus
sanguineous, its outer area and apex black.
Long. 5 mm.
Hab. Transvaal: Zoutpansberg (Junod, Brit. Mus.).
Camptobrochis capensis, sp. n.
Reddish ochraceous ; head and scutellum black, the last
with a central reddish-ochraceous fascia, which does not reach
the base ; antenne, lateral margins of corium, tibie, and tarsi
pale ochraceous; apices of tarsi black; antennee somewhat
slender, second joint more than twice the length of first ;
pronotum distinctly punctate, anterior and posterior margins
narrowly ochraceous, the last linearly transversely black
near lateral angles; scutellum and corium more finely and
obscurely punctate than pronotum ; corium and clavus some-
what longly pilose ; membrane fuscous, with paler mottlings.
Long. 4mm.
Hab. Cape Colony: Grahamstown (Albany and Brit.
Muss.).
Division BRYOCORARIA.
Genus TENTHECORIS.
Tenthecorts, Scott, Ent. Month. Mag. xxxiii. p. 65 (1886).
Type, Z. bicolor, Scott (Brit. Mus.).
This genus is very closely allied to Hecritotarsus, Stal. It
is described as an orchid pest, as is also Hecritotarsus exiti-
osus, Dist., and EH. orchidearum, Reut. T. bicolor is very
closely allied by description to Reuter’s species; Scott
describes the first and second joints of the antenne as red,
but in one of his typical specimens the apex of the first joint
and the whole of the second joint are distinctly black.
Division @
Genus FUNDANIUS.
Fundanius alternus.
Capsus alternus, Walk. Cat. Het. vi. p. 111. n. 252 (1873).
Resthenia alternus, Atkins. Cat. Capside, p. 57 (1890).
i?
Division
Genus ARMACHANUS.
Armachanus spicaius, sp. n.
Uniform pale cinnamon-brown ; a discal, transverse, pale
greyish line across apex of clavus, and an oblique line of the
same colour crossing corium near middle; a prominent black
tn the British Museum and elsewhere. 203
marginal spot near middle of corium and a larger black spot
to cuneus ; head with a long, porrect, anterior, central spine ;
first joint of antenne a little more than half the length of
second ; pronotum strongly constricted and depressed before
middle; scutellum carinately tumid; hemelytra obliquely
depressed on each side, the sutures forming a central longi-
tudinal carinate ridge; posterior area of the corium before
cuneus semiglobose.
Long. 5 mm.
Hab. N.W. Australia: Adelaide River (J. J. Walker,
Brit. Mus.).
The genus Armachanus is described and its type figured in
my second volume on the Rhynchota of British India, which
will shortly be published. The typical species was from
Ceylon.
Division PLAGIOGNATHARIA.
DAGBERTUS, gen. nov.
Head somewhat large and subtriangular above, deflected
anteriorly, where it is conically produced, and a little laterally
compressed ; eyes of moderate size, almost touching, but
projecting a little beyond the anterior angles of the pronotum ;
antennz slender, first joint about as long as head and stouter
than the other joints, second about or a little more than twice
the length of first, third and fourth slender, tomentose, third
longer than fourth ; rostrum long, passing the posterior coxee ;
pronotum trapezoidal, the posterior lateral angles slightly
subacutely produced, posterior margin slightly convex and
about twice as broad as anterior margin, lateral margins
nearly straight; scutellum subtriangular, about as long as
the pronotum ; hemelytra subhyaline, lateral margins almost
parallel, a little rounded; posterior femora moderately in-
crassate, remaining legs mutilated in the types of the three
representative species.
This genus may be placed near Episcopus, Reut.
Dagbertus Darwini.
Capsus Darwini, Butl. Proc. Zool. Soc. 1877, p. 89.
Hab. Galapagos; Charles Island (C. Darwin, Brit. Mus.).
Dagbertus quadrinotatus.
Capsus quadrinotatus, Walk. Cat. Het. vi. p. 113. n. 256 (1873).
Resthenia quadrinotatus, Atkins. Cat. Capside, p. 61 (1890).
Rostrum passing the posterior cox ; not ‘ reaching’ same,
as described by Walker.
204 Mr. W. L. Distant on Capsides
Dagbertus ? spoliatus.
Capsus spoliatus, Walk. Cat. Het. vi. p. 112. n. 254 (1878).
Resthenia spoliatus, Atkins. Cat. Capside, p. 61 (1890).
This species is represented in the National Collection by
six very imperfect specimens. TExact generic identification
is out of the question.
Capsus obscurellus, Walk. Cat. Het. vi. p. 93. n. 154 (1873).
Type in such a mutilated condition as to be undeterminable.
Monalenion divisum, Walk. Cat. Het. vi. p. 163. n. 9 (1873).
The type is headless. Probably represents an undescribed
genus with affinities to the Neotropical Resthenta.
Capsus tntaminatus, Walk. Cat. Het. vi. p. 127, n. 304
(1873).
In the four specimens representing this species there are
contained three distinct genera; but the specimens are all
mutilated, the type cannot be fixed, and the species must be
regarded as non-existent,
Summarized Disposition of Walker's Genera and Species.
Capside.
Species considered valid and described under correct Genera.
Monalonion braconoides, Walk. Cat. Het. vi. p. 162 (1878).
Eucerocoris braconoides, Walk. loc. cit. p. L64.
basifer, Walk. loc. ert.
Helopeltis niger, Walk. loc. cit. p. 165.
Species considered valid, but requiring generic revision.
Lopus partilus, Walk. Cat. Het. vi. p. 56 (1878), belongs to gen, Araspus,
g.n.
australis, Walk. loc. crt. p. 57, belongs to gen. Pantilius, Curtis.
sordidus, Walk. loc. ctt., 4 Sabellicus, g. n.
Capsus incisus, Walk. loc. cit. p. 92, 3 Resthenia, Spin.
-— coccineus, Walk. loc. cit. p. 93, oe Lomatopleura, Reut.
—— limbatellus, Walk. loc. ctt., ~ Peecilocapsus, Reut.
— strigulatus, Walk. loc. cit. p. 94, * Camptobrochis, Fieb.
—— filicornis, Walk. loc. cit. p. 96, Megacelum, Fieb.
—— marginatus, Walk. loc. cit., Ss Peecilocapsus, Reut.
floridanus, Walk. loc. cit. p. 97, a Lopidea, Uhler,
scitulus, Walk. loc, cit. p. 99, a Lopidea, Uhler.
— opacus, Walk. loc. ert. p. 100, ‘ Calocoris, Fieb.
—— jamaicensis, Walk. loc, cit. p. 101, ,, Resthenia, Spin.
in the British Museum and elsewhere. 905
Capsus basalis, Walk. Cat. Het. vi. p. 108 (1873), belongs to gen. Ites-
thenia, Spin.
—— tibialis, Walk. Zoe. cit. p. 109, belongs to gen. Sysinas, Dist.
-— atroluteus, Welk. loc. cit., a Resthenia, Spin.
—— wanthophilus, Walk. loc. cit. p. 110, ,, Monalonion, Uerr.-
Schatf.
— squalidus, Walk. loc. cit., 95 Horcias, Dist. ?
— incertus, Walk. loc. cit. p. 111, Pe Megacelum, Vieb.
— obumbratus, Walk. loc. cit., o Hlorcias, Dist.
— alternus, Walk. loc. cit., r Fundanius, Dist.
— leprosus, Walk. loc. cit., 5 Paracalocoris, V:st.
— spoliatus, Walk. loc. cit. p. 112, rr Dagbertus, g. 0.
— quadrinotatus, Walk. loc. cit. p. 118, ,, Dagbertus, g.n.
— sobrius, Walk. oc. cit. p. 115, ‘ Paracalocoris, Dist.
—— illepidus, Walk. loc. cit., 3 Lygus, Uahn.
— solitus, Walk. loc. cit. p. 116, is Peciloscytus, Fieb.
— pallidulus, Walk. loc. ctt., i Lygus, Hahn.
—— conspersus, Walk. loc, cit., a Lygus, Wabn ?
— suffusus, Walk. loc. eit. p. 117, 9) Lygus, Hahn.
— seritceus, Walk. loc. ett., “5 Paracalocoris, Dist.
— partitus, Walk. loc. cit. p. 119, F Liocoris, Fieb.
— stramineus, Walk. loc. cit. p. 120, ,, Megacelum, FVieb.
— patulus, Walk. loc. cit., 5 Dereocoris, Kirschh.
sinicus, Walk. loc. cit., > Megacelum, Fieb.
— vicarius, Walk. loc. ett. p. 121, - Rhinomiris, Wirk.
— incisuratus, Walk. loc. cit., + Argenis, g. .
Jasciatus, Walk. loc. cit. p. 122, aS Disphinctus, Stal.
discotdalis, Walk. loc. cit., 4 Malacopeplus, Wirk.
apicifer, Walk. loc. czt. p. 124, . Sabellicus, g. n.
— lucidus, Walk. loc. cit., 5 Kosmiomiris, Wark.
— simulans, Walk. loc. cit. p. 125, 7 Bothriomiris, Wirk.
— tristis, Walk. loc. cit., He Saturnioniris, Kirk.
angulifer, Walk. loc. cit. p. 126, - Megaceélum, Fieb.
pretulifer, Walk. loc, cit., <5 Zanessa, Kirk.
laticinctus, Walk. loc. cit. p. 127, _ ,; Calocoris, Fieb.
Leptomerocoris maoricus, Walk. loc. cit. p. 146, belongs to gen. Lygus,
Hahn.
Monalonion politum, Walk. loc. cit. p. 163, belongs to gen. Disphinctus,
Stal.
— divisum, Walk. loc. cit., belongs to gen. ? (type headless).
Species treated as synonymic.
Capsus xanthomelas, Walk. Cat. Het. vi. p. 92 (1873), = Resthenia mnsitiva,
Say.
hirsutulus, Walk. loc. cit. p. 95,= Neurocolpus nubilus, Say.
contiguus, Walk. loc. cit.,= Calocoris norvegicus, Gmel.
stramineus, Walk. loc. cit. p. 96, = Calocoris norvegicus, Gmel.
decoratus, Walk. loc. cit. p. 100, = Pecilocapsus ornatulus, Stal,
bicinctus, Walk. loc. cit.,= Resthenia ornaticollis, Stal.
einctipes, Walk. loc. cit. p. 109,= Horcias Signoreti, Stal.
innotatus, Walk. loc. cit. p. 116,= Lygus australis, Dist., nom. n.
limbatus, Walk. loc. cit. p. 117,= Lygus ethiops, Dist., nom. n.
canescens, Walk. loc. cit. p. 121,= Rhinomiris vicarius, Walk.
- —— lineifer, Walk. loc. cit. p. 122,= Hyalopeplus vitripennis, Stal.
— ustulatus, Walk. loc. cit. p. 128,= Calocoris laticinctus, Walk.
MELT T TA
206 Mr. O. Thomas on new Bats from
Leptomerocoris antennatus, Walk. loc. cit. p. 145,=Sabellicus sordidus,
Walk.
Helopeltis braconiformis, Walk. loc. cit. p. 165,=Helopeltis (Dulichius)
clavifer, Walk.
To be treated as non-existent.
Types broken, undeterminable.
Capsus obscurellus, Walk. Cat. Het. vi. p. 95 (1873).
intaminatus, Walk. loc. cit. p. 127.
Species the types of which are not now to be found in the British Museum.
Capsus frontifer, Walk. Cat. Het. vi. p. 94 (1873).
pallescens, Walk. loc. cit.
nigritulus, Walk. loc. cit. p. 112.
semiclusus, Walk. loc. cit. p. 118.
subirroratus, Walk. loc. eit. p. 119.
marginicollis, Walk. loc. ert. p. 128.
Leptomerocoris simplea, Walk, loc. cit. p. 145.
Monalocoris bipunctipennis, Walk. Joe. cit. p. 159.
Monalonion ichneumonoides, Walk. loc. cit. p. 162.
XXII.—New Bats from British East Africa collected by Mrs.
Hinde, and from the Cameroons by Mr. G. L. Bites. By
OLDFIELD ‘THOMAS.
THe British Museum owes to the kindness of Mrs. Hinde,
wife of Dr. 8. L. Hinde, of Fort Hall, British East Africa,
a further collection of bats, and these include three well-
marked new forms, which I have described below, in con-
junction with two others obtained by Mr. G. L. Bates in
West Africa.
The new Myotis from Fort Hall, which I have named in
honour of its captor, is an especially noticeable discovery.
Pipistrellus crassulus, sp. n.
A medium-sized species with disproportionally short fore-
arms.
General build thick and heavy. Muzzle broad, swollen.
Ears short, laid forward they do not nearly reach to the tip
of the muzzle; inner margin straight below, convex above ;
tip evenly and broadly rounded; outer margin straight
above, slightly convex below; basal lobe small, rounded.
Tragus of medium length, its greatest breadth opposite its
British East Africa and the Cameroons. 207
inner base; inner margin straight, tip rounded, outer margin
gently convex, ending below ina small basal lobule. Thumbs
short, with thickened but not enlarged basal pad. Wings from
the base of the toes. Calcars about equal in length to the
free border of the uropatagium ; postcalcareal lobules distinct
but narrow. ‘Tail involved in membrane almost to the tip.
Penis very long, slender.
Fur 3°5-4:0 mm. long on back. Uniformly dusky brown
above, scarcely paler below. Membranes blackish brown
throughout, without any trace of white margins.
Skull broad, stout and flattened, conspicuously broader and
heavier, especially anteriorly, than in P. pipistrellus, which
has a much longer forearm. Upper profile straight, the
frontal region not inflated.
Inner upper incisors very thick, bifid ; the postero-external
cusp nearly as long as the main one ; outer incisor slender,
unicuspid, reaching about halfway from the cingulum to the
tip of the inner tooth. Small upper premolar in the inner
angle between the canine and large premolar, which touch
one another outside it; not visible from without. Lower
incisors broad, bifid. First lower premolar about three
fourths the height of the second.
Dimensions of the type (measured in spirit) :—
Forearm 28 mm.
Head and body 47; tail 27; ear 10; tragus on inner
edge 3°5 ; thumb, free of membrane (c. u.) 4; third finger,
metacarpus 26, Ist phalanx 9, 2nd phalanx 8°8 ; fifth finger
37; lower leg 12; hind foot, from back of calcar (c. u.) 7;
penis 11.
Skull: greatest length 12:7; mastoid breadth 7:7.
Hab. Efulen, Cameroons.
Type. Adult male. Collected by G. L. Bates. One
specimen.
This bat, with the short forearm of such pigmy species as
Pipistrellus Stampflii and minusculus, has a very much larger
body and head. The breadth and flatness of the skull are
particularly noticeable.
Scotophilus nigrita colias, subsp. n.
A richly yellow (almost orange) bellied race of 8. négrita,
General characters as in this species, which is Dobson’s
“8. borbonicus.” Fur long, rather shaggy ; hairs of back
8-9 mm. in length. General colour above (of the tips of the
hairs) olivaceous, but the bases of the hairs are a dull sulphur-
yellow, which shows through on the upper surface, Below,
208 Mr. O. Thomas on new Bats from
the central line is a rich chrome-yellow, deepening laterally
on the sides of the belly to a golden yellow, which is especially
bright on the broad band of fur extending on the wing-
membrane between the elbows and knees.
Dimensions of the type :—
Forearm 55 mm. (57 in a second specimen).
Skull: greatest length 20°5; zygomatic breadth 14°5 ;
cheek-tooth series 5:7.
Hab, Fort Hall, Kenya District, British East Africa.
Type. Male. B.M. no. 2.7.6.11. Original number 107.
Collicted 25th Jan., 1902, and presented by Mrs. Hinde.
The bats referable to S. nigrita seem divisible by colour
into several geographical subspecies, of which S. n. Ding zn,
Smith, would be the Cape one, and S. n. leucogaster, Cretzschm.,
the Abyssinian. Specimens representing the true Senegalese
S. nigrita and the Mozambique forms described by Peters
are still wanting to the Museum Collection.
From any member of the group as yet described S. n. colias
seems readily distinguishable by its brilliantly yellow under
surface.
Scotophilus nigrita nux, subsp. n.
A chestnut-brown subspecies of S. nigrita.
General characters of the smaller forms of the widely
distributed S. nzgrita. Fur short, close and fine; hairs of
Lack about 5mm. in length. Colour above uniform chestnut-
brown, or “burnt umber” (Ridgway), the bases of the hairs
slightly paler than the tips; very different therefore from the
other pale brown or olivaceous representatives of the species.
Under surface a rather lighter brown, approaching “ russet”’
(Ridgway), the other forms being all yellowish or whitish
below. Fur of body scarcely extending on the wing-membranes
below.
Dimensions of the type (measured in spirit bcforeskinning ):—
Forearm 55 mm.
Head and body 70; tail 47; ear 15.
Skull: greatest length 20°5 ; zygomatic breadth 14°7 ;
upper cheek-tooth series 5:8,
flab. Kfulen, Cameroons.
Type. Adult male. B.M. no. 3. 2. 4. 5. Collected by
Mr. G. L. Bates.
Although conspicuously different in colour from any of
the known forms of S. nigrita, this bat so clearly represents
that species in the West-African forest country that for the
resent I prefer to give it only subspecific rank.
British East Africa and the Cameroons. 209
Myotis Hildegardece, sp. n.
A beautiful and brightly coloured species allied to
M. Bocaget.
Size medium. Lars small, narrow; inner margin evenly
convex, tip very narrowly rounded, outer margin concave
above, convex below, a marked angular antitragal lobule at the
outer base thickly covered with fur. Tragus rather short, its
inner margin slightly but evenly convex, its greatest breadth
opposite the lower third of its inner margin, whence it slopes
evenly to the narrow but not sharply pointed tip; basal lobe
large, rounded. Feet large; wings to the metatarsi ; calcars
long, reaching nearly three-fourths towards the tip of the tail
and ending in a distinct lobule.
Fur soft, thick and fine; hairs of back about 5-6 mm. in
length. Wing-membranes naked, except for a few hairs on
the under surface between the humeri and the flanks. Inter-
femoral furry above at the base, a narrow band _ passing
outwards behind the legs nearly halfway down the tibie. Top
of toes hairy.
General colour of upper surface bright “ tawny-ochraceous,”
the head rather paler than the back. Individually the hairs
are blackish brown for about 2 mm. at their bases, then pale
tawny, darkening to their tips. Below the general colour is
“ pinkish-buff,” the hairs blackish at their bases. Membranes
dark throughout, contrasting strikingly with the bright
colour of the body.
Skull considerably larger than in M. Bocagei, broader and
lower than in M. Goudott. Small upper premolars in the
tooth-row, subequal in horizontal section, and less unequal in
height than usual.
Dimensions of the type (measured in skin) :—
Forearm 37 mm.
Head and body (c.) 55; tail 37 ; ear (dry) 13; tragus on
inner edge (dry) 4°6 ; thumb clear of membrane 5 ; third
finger, metacarpus 385, Ist phalanx 15°5, 2nd phalanx 10°7 ;
fifth finger 53 ; tibia 17 ; foot from back of calcar (c. u.) 9°8;
calcar 17.
Skull: greatest length 15°2; basal length 11:3; breadth
of brain-case 8; front of canine to back of m* 5°7.
Hab. Fort Hall, Kenya District. Alt. 4000 feet.
Type. Male. B.M. no. 3.3.2.2. Original number 115.
Collected 17th Oct., 1902, by Mrs. Hinde. Two specimens.
This very beautiful bat I have much pleasure in naming in
honour of its discoverer Mrs. Hildegarde Hinde, to whom
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 14
210 On new Bats from British East Africa, ke.
the British Museum is indebted for so many interesting
Chiroptera and Rodentia.
M. Hildegardee is readily distinguishable from any of its
allies by its striking coloration, as it is far brighter in tone
than either 17. Bocaged or M. Goudoti, the species most similar
to it.
Nyctinomus Hindet, sp. n.
A whitish-winged member of the VV. pumilus group.
Essential characters of ears, tragus, skull, &e., apparently
as in JV. imbatus, Peters. A marked tuft of brown hairs
behind the joining membrane of the ears.
Colour of upper surface chocolate-brown, finely flecked
with white; the bases of the hairs (which attain about
4-4°5 mm. in length) rather lighter. Under surtace brown,
more or less washed superiicially with whitish, especially
along the middle line of the belly ; a creamy white line
edging the junction of the wings with the flanks. Lars,
forearms, hind limbs, and interfemoral membrane dark brown.
Wing-membranes near the body whitish brown, paling to
white on the middle part of the wing, and darkening again
at the tips to brown.
Skull about as in NV. Hminz, though with less marked pre-
orbital processes. Small upper premolar outside the middle
line of tooth-row, less crushed than in limbatus, more so than
in Emini. Middle lower incisors deeply bifid.
Dimensions of the type (measured in skin) :—
Forearm 40 mm.
Head and body (c.) 61; tail 835; thumb close to membrane
6; third finger, metacarpal 39, Ist phalanx 15°5; fifth
finger 39.
Skull: greatest length 17°6; basal length 14:6; zygomatic
breadth 11°4 ; front of canine to back of m* 6°7.
Hab. Fort Hall, Mt. Kenya district, British East Africa.
Alt. 4000 feet.
Type. Adult male. B.M. no. 3.3.2.4. Original number
134. Collected 1st Jan., 1903, and presented by Mrs. Hinde.
Two specimens.
This Nycténomus is most closely related to N. Emini,
de Wint., of Usambiro, German EH, Africa *, but differs by
its whitish wings and more closely crushed upper premolars.
* Not Mosambiro, as accidentally printed in the original description,
Ann. & Mag. Nat. Hist. (7) vil. p. 41 (1901).
On new Hymenoptera from Northern India. Pla
XXIII.—Descriptions of new Species of Aculeate and
Parasitic Been ODIETE from Northern India. By P.
CAMERON.
Apide.
Nomia pilosella, sp. n.
Black; the head, thorax, base of abdomen, and legs
densely covered with longish white pubescence; the second,
third, fourth, and fifth segments with emerald-coloured
smooth bands; postscutellum with two stout longish black
spines; metanotal area stoutly closely striated. Wings
hyaline, the apex infuscated ; tegule black, pale round the
outer border. Face and clypeus not very strongly keeled
down the middle. Hind femora roundly dilated above, the
basal slope longer and not so long as the apical; the hind
tibiz become gradually wider towards the apex and rounded
on the outer side; on the inner side the basal two thirds is
straight, only slightly roundly dilated; the apex is broadly
bluntly roundly dilated, somewhat as in N. Westwoodi, but
the femora are much ‘thicker, more dilated in the centre
above, the basal and apical ‘slopes are straight, oblique,
whereas in Westwoodi the temora above have a gradually
rounded curve from the base to the apex ; in the present
species they are shaped more as in N. Elliotii as figured by
emis (lrans.’ Ent) Soc. 1875, pl. 1, fig:*7), but not by
Bingham (‘ Fauna of Brit. India,’ 1. p. 449). The pubescence
on the present species is much longer and denser than in
Elliotii, which has the base of the metanotum “ finely punc-
tured,” and there is a green band on the first abdominal
segment; the present species has no band on it and the base
of the metanotum is stoutly reticulated; also it is much
more densely pilose.
Hab. Khasia Hills. Coll. Rothney.
Habropoda fulvipes, sp. n.
Black; the basal two segments of the abdomen rufo-
fulvous, the lower inner orbits, a dagger-shaped mark (the
“ handle” above) on the centre of the face and clypeus, apex
of clypeus, labrum, and basal half of mandibles pale yellow ;
the hair on the front of the head darker, behind paler coloured
than it is on the thorax; antenne dark brownish; legs
14*
212 Mr. P. Cameron on new
fulvous, with paler hair. Wings hyaline, slightly tinged
with fulvous; the nervures and stigma black. ?¢?.
Length 14 mm.
Hab. Khasia Hills. Coll. Rothney.
Clypeus punctured; in its centre a stout keel which
reaches near to the apex; the face tuberculate in the middle,
its apex and that of the labrum margined ; on the centre of
the face at the apex is a broadly triangular yellow-fulvous
mark; on either side of the top of the labrum is a brownish
mark, with two projections, the inner of which is raised.
There is a dark brownish plate on the outer side of the base
of the hind tibiz, which is longer than broad, shield-shaped,
roundly narrowed towards the apex, and with the outer edges
raised. Basal four abdominal segments fringed with pale
fulvous hair, the apical with longer black hair all over; the
pygidium bare, with the sides broadly depressed on the apical
half. Vertex smooth and shining, the front punctured, with
a narrow keel down the centre.
What I suppose is the male has the head black, except the
clypeus, which is pale yellowish testaceous ; the lower part of
the front and the sides of the clypeus thickly covered with
depressed fulvous pubescence, as is also the greater part of
the thorax ; the abdomen above is black except the base and
apices of the basal two segments broadly, and the ventral
surface, which are honey-coloured; the legs are similarly
coloured, except that the coxz, trochanters, femora, and hind
tibiz are black above; the hind femora become gradually
roundly dilated from the base to the apex ; the hind tibiz
curved, not swollen. Clypeus margined laterally, not very
convex, its apex transverse, margined narrowly on the inver
edge. Antenne entirely black. The wings are more clear
hyaline than in the female, and the nervures and stigma are
lighter coloured.
Compared with Bingham’s figure of H. Magrettii the male
of the present species has the thorax only very slightly haired
and the hind femora are not at all so strongly dilated ; its
abdomen, too, is longer and narrower. It (the male) appears
to be much more slenderly built than any species of Habro-
poda I have seen, is much less hairy, and has a much longer
malar space, the eyes being widely distant from the base of
the mandibles. The third joint of the antennez is swollen,
not uarrowed at the base, and is hardly so long as the
fourth, whereas in what I take to be the male of H. Radosz-
kowskii it is clearly longer and distinctly narrowed at the
base. In neither the female nor the male of my species is
the second recurrent nervure interstitial. The Indian species
Hymenoptera from Northern India. OTS
of Habropoda can hardly be looked upon as typical of the
genus. Possibly my male represents a distinct species. It
certainly appears to be too slender for the female, comparing
it with the males of other species of the genus and their
females.
Celioxys cariniscutis, sp. n.
This species is very similar to C. khasiana, with which it
agrees in size, form, and coloration, including the fulvous
pubescence on the underside of the tarsi, but it differs in the
clypeus beg keeled down the centre, in the sides of the
scutellum being deeply furrowed, with the outer edge raised ;
the lateral teeth are stouter, depressed in the centre, become
narrowed gradually to the apex, which is rounded and not
depressed ; the pronotum at the base projects into a large
plate, which becomes gradually narrowed outwardly, forming
a triangle of which the upper side is longer than the lower.
There are eight teeth on the apical segment, two basal and
six apical; the upper central pair are the shorter ; the space
behind them is depressed, the base of the depression with an
oblique slope and shallower than it is at the apex ; the apical
lower pair of teeth are much longer and stouter than the
others; the apices of the third, fourth, and fifth segments
are less closely punctured than the rest; there is an oblique
furrow on the sides of the second near the base and an
oblique depression on the sides of the fifth near the base ;
the ocellar region has some smooth spaces at the sides and
behind the ocelli; the lateral teeth of the scutellum are not
bent downwards as in khasiana and basalis; the wings are
fuscous violaceous to the transverse basal nervure. <.
Length 11-12 mm.
Hab. Khasia Hills. Coll. Rothney.
Celioxys khasiana, sp. n.
Black ; clypeus, face, lower part of the vertex broadly on
the sides, pleurze, metanotum, and the apices of the abdo-
minal segments narrowly covered with white pubescence, the
rest of the head and thorax with short white pubescence ;
wings bright dark fuscous violaceous, highly iridescent, the
nervures and stigma black. 9@.
Length 11-12 mm.
Hab. Khasia Hills. Coll. Rothney.
Vertex covered with large, deep, round punctures, which
are much more widely separated at the sides of the ocelli ;
the raised central part of the front more coarsely punctured,
14 Mr. P. Cameron on new
almost reticulated ; its sides more closely and less coarsely
punctured ; face and clypeus closely irregularly punctured ;
the hair fringing the apex of the clypeus has a fulvous
tinge. Mandibles to near the apex coarsely punctured,
the punctures longish. Pro- and mesothorax closely covered
with large deep punctures, which are small on the base of
the mesonotum. Apex of scutellum broadly rounded ; the
lateral teeth large, almost smooth, curved down slightly at
the apex. Median segment and apex of mesopleurz smooth.
Abdomen sparsely but distinctly punctured; the apex of the
last segment closely rugosely punctured, the centre raised,
smooth, the sides obliquely depressed ; the apex becomes
gradually narrowed to a point; the apical ventral segment
becomes gradually narrowed and projects largely beyond the
upper. Legs covered with white pubescence; the tarsi
below with longish stiff fulvous hair.
Comes near to C. basalis, Sm.
Nomia Rothneyi, sp. n.
Black ; an interrupted band of white pubescence on the
apex of the first abdominal segment; a broad smooth white
band on the apices of the second, third, and fourth segments ;
flagellum of antennz brownish beneath ; wings hyaline, the
stigma testaceous, the nervures darker coloured. @.
Length 7 mm.
Hab. Mussoorie (Rothney).
Face broadly roundly raised in the middle; clypeus
opaque, with clearly separated scattered punctures, its apex
transverse; front and vertex closely punctured; an im-
pressed line on the centre of the upper three fourths of the
front; the sides of face, of the front, and the outer orbits
thickly covered with white pubescence. Thorax closely
punctured; the sides and apex of the mesonotum and the
postscutellum thickly covered with grey pubescence. Basal
area of metanotum large, clearly defined, strongly trans-
versely striated ; the striz distinctly separated ; the narrowed
basal inner edges obliquely striated. Pleure, sternum, and
legs densely covered with long cinereous pubescence. Abdo-
men smooth and shining; there is a transverse, curved,
impressed line behind the white band on the third and fourth
segments; the apical two segments are brown.
This species cannot well be confounded with any of the
described white-banded species of Paranomia.
Cr
Hymeneptera from Northern India. 21
Nomia interrupta, sp. n.
Black ; a narrow line of pale green on either side of the
apex of the second abdominal segment, the tibiz rufous ;
the pleurz densely covered with long fulvous pubescence,
the mesonotum more sparsely with shorter black, the cheeks
with pale fulvous, the face and clypeus with fulvous pubes-
cence. Flagellum of antenne for the greater part rufo-
testaceous. Wings hyaline, slightly tinged with fulvous.
Face and clypeus stoutly keeled down the centre. ?.
Length 13 mm.
Hab. Khasia Hills. Coll. Rothney.
Face distinctly projecting in the middle, the projection
with an oblique slope, almost smooth ; the clypeus distinctly
sparsely punctured; the central keel on the two is con-
tinuous. Clypeus roundly convex, its apex broadly roundly.
Front and vertex sparsely indistinctly punctured. Meso-
notum closely and distinctly punctured, the scutellum as
closely but not so strongly. Basal area of metanotum closely,
strongly, irregularly transversely striated. Tegule rufo-
testaceous. Back of abdomen minutely punctured, except at
the apex of the segments ; the scopa bright rufous. Hair
on legs long, fulvous, glistening on the tibize and tarsi.
A distinct species, easily known by the single, interrupted,
smooth, greenish band on the second abdominal segment,
strongly keeled face and clypeus, and the four rufous front
tibize.
Nomia tuberculata, sp. n.
Black ; the pubescence on the head, thorax, and underside
of the abdomen pale fulvous; the base of the first abdominal
segment thickly covered with fulvous pubescence, the rest of
the pubescence on the back short, sparse; the apices of the
basal three segments broadly smooth and shining. Face
roundly dilated in the centre, almost smooth ; the clypeus
broadly depressed in the middle, the sides roundly dilated,
smooth and shining, bearing some large punctures; the top
in the centre keeled, the apex is transverse, clearly separated.
Wings hyaline, the apex with a fuscous cloud ; stigma and
nervures testaceous. ?.
Length 13 mm.
Hab. Khasia Hills. Coll. Rothney.
Face, front, and vertex sparsely punctured, the face in the
centre smooth. Postscutellum thickly covered with fulvous
pubescence. Median segment smooth and shining, its basal
216 Mr. P. Cameron on new
area not defined, its sides with a few keels. Tegule testa-
ceous. ‘The hair on the legs is long, dense, and fulvous, the
spurs dark rufous.
Characteristic of this species is the fact that the raised
centre of the face and the sides of the clypeus form three
large tubercles. In Bingham’s arrangement (‘ Fauna of
Brit. India,’ Hym. i. p. 459) it comes near N. terminata, Sm.
Megachile khasiana, sp. n.
The pubescence on the head, thorax, and base of abdomen
dense, fulvous, on the rest of the back of abdomen and on
the apex of ventral surface black; on the base the ventral
scopa black; legs covered with cinereous pubescence; the
pubescence on the underside of the base of four front tarsi
rufous, on the hinder black ; wings fuscous violaceous, the
base more hyaline, paler. 9¢.
Length 13 mm.
Hab. Khasia Hills. Coll. Rothney.
Face and clypeus strongly but not closely punctured, the
pubescence on them paler and sparser than on the front.
Mandibles widely furrowed along the outer edge ; the apical
part bordered by a narrow curved furrow, the central with
some irregular furrows, of whieh the apical is the wider and
deeper; the apical tooth is long and stout, rounded at the
apex, the second is broader and shorter and becomes
gradually narrowed to the apex, which is rounded; the rest
is broadly bluntly rounded and toothless. Abdomen opaque,
closely punctured ; the basal three segments have transverse
furrows near the middle, the apex of the third is more widely
depressed. Calcaria testaceous; metatarsus nearly as wide
as the tibiz ; apex of clypeus transverse.
Of the Indian species this comes nearest to M. umbripennis,
Sm., recorded by Smith from Borneo and Nepaul and by
Bingham from Sikhim and Tenasserim. The number of
mandibular teeth is not given by Bingham, but Smith states
(Cat. Hym. Brit. Mus. i. p. 175) that they have four stout
teeth, so his species is readily separated from M. khasiana.
FossoreEs.
Trypoxylon placidum, sp. ni.
Black; the antennal scape, face, and clypeus thickly
covered with silvery pubescence, the pleure, sternum, and
median segment with longish white hair, the pro- and
Hymenoptera from Northern India. 217
mesonotum thickly with long fuscous hair, the legs sparsely
with white pubescence. Wings hyaline, the apex smoky,
nervures and stigma black. Apical joint of antenne
thickened, nearly twice the length of the preceding two
joints united. Front alutaceous, indistinctly furrowed in
the centre ; vertex opaque, finely, not very distinctly punc-
tured. Clypeus not carinate in the middle, its apex broadly
rounded, raised, smooth. Palpi pallid testaceous, black at
the base. The apex of metanotum has an oblique slope ;
the basal furrow extends from the base to the apex, becomes
gradually wider, is shallow and finely transversely striated ;
the furrow on apical slope wide, deep on the basal half,
V-shaped ; the apical third of the segment is somewhat
coarsely transversely striated. Abdominal petiole narrow,
with only the apex dilated; it is as long as the succeeding
three segments united, its apex distinctly clavate. 9? @.
Length 13 mm.
Hab. Khasia Hills. Coll. Rothney.
Trypoxylon fulvocollare, sp. n.
Black ; the basal five or six joints of the antennz fulvous,
the scape thickly covered with white hair, the flagellum with
shorter blackish pubescence ; clypeus and mandibles rufous,
palpi pale testaceous ; the apex ef pronotum and tubercles
fulvous ; the base and sides of the first abdominal segment
and the base of the second and third segments broadly rufo-
testaceous. Apex of fore cox, trochanters, femora, tibiz,
and tarsi fulvous, the femora of a deeper hue, the apex of
the middle femora, the middle tibiz and base of tarsi, and
the base of the hinder tibize pale testaceous. Wings hyaline,
with a slight fulvous tinge, the costa and stigma fulvous,
the latter lighter in tint; the radius and cubitus testaceous.
Face, eye-incision, outer orbits and the base, sides and apex
of mesonotum thickly covered with golden pubescence; the
scutellum with short fuscous, the postscutellum with longer
fulvous hair; the pleurze and sternum with short pale fulvous
pubescence. Front and vertex sparsely punctured, the
former above with a wide and shallow furrow; the lower
half triangularly keeled. On the apex of the basal half of
the median segment is an elongated fovea; the apical half
deeply furrowed in the middle. The apical third of the
petiole dilated.
Comes nearest to T. coloratum, Sm.; that species has only
a small tubercle above the base of the antenne, while in the
present species there is not a tubercle, but a long stout
218 Mr. P. Cameron on new
keel. There is no lateral furrow on the base of the median
segment. &.
Length 17-18 mm.
Hab. Khasia Hills. Coll. Rothney.
Trypoxylon khasie, sp. n.
One of the larger species. In size comes near to T. colo-
ratum, which differs in having the pubescence golden. In
Bingham’s table (‘ Fauna of Brit. India,’ Hym. 1. p. 224) it
comes into B, except as regards the size and 6°. “ Abdomen
red, basal segment only black.”
Black ; apex of clypeus testaceous ; mandibles yellow, their
teeth black ; palpi yellow ; scape and base of flagellum of
antenne pale yellow, the rest black, brownish beneath; the
base and sides of mesonotum with a distinct fulvous-yellow
band; tubercles yellow, except at the base, and fringed with
silvery hair; abdomen rufo-testaceous, the petiole black,
except at the apex, the black there being triangularly incised
in the middle. Four front legs yellowish, the femora of a
more testaceous hue, the base of all the coxe black ; the
hind femora black, running into testaceous towards the
middle; the hinder tibize yellowish beneath, flavo-testaceous
above, blackish towards the apex, the tarsi blackish, the
apices of all the joints testaceous. Wings hyaline, the stigma
testaceous. The clypeus, orbits, and eye-incision densely
covered with silvery pubescence; the front obscurely punc-
tured; a narrow furrow runs from the ocelli. Thorax
densely pilose, the pile fuscous on the mesonotum, longer
and more silvery on the sides; the sides and apex of median
segment thickly covered with pale hair; at its base in the
middle is an elongated somewhat pear-shaped depression ;
the apex is deeply and widely furrowed and densely covered
with long white hair. The greater part of the pleurz covered
with silvery pubescence.
Length 20 mm.
Hab. Khasia Hills. Coll. Rothney.
Trypoxylon orientale, sp. n.
Antenne black, distinctly thickened towards the apex, the
scape thickly covered with long white hair; flagellum bare.
Face, lower part of eye-incision, and clypeus thickly covered
with silvery pubescence ; front and vertex opaque, covered
with long fuscous hair. Palpi pale testaceous. Thorax
thickly covered with pale hair. Median segment short, its
apex with an oblique slope ; on the base is a striated depres-
Hymenoptera from Northern India. 219
sion, which becomes gradually wider towards the apex and is
moderately deep; there is a smooth, narrower, oblique
furrow on the sides. Legs black, pilose, the hair on the
femora longer. Wings clear hyaline, the sides of the dilated
apex of the petiole and the base and sides of the second
segment rufous ; the petiole long and slender, as long as the
following three segments united. 2.
Length 22 mm.
Hab, Khasia Hills. Coll. Rothney.
Psen rufo-balteata, sp. n.
Black ; the apex of the second abdominal segment and
the whole of the third rufous; the fifth and following joints
of the antenne testaceous beneath. Legs thickly covered
with white hair; the spurs pale rufous. Wings clear hyaline ;
the first cubital cellule in front is half the length of the
second, the first recurrent nervure is received very near the
first transverse cubital, the second at twice the distance from
the second transverse cubital. 92,
Length 5 mm.
Hab. Khasia Hills. Coll. Rothney.
Antenne stout, thickened towards the apex; the scape
beneath sparsely covered with long black hair. Face and
clypeus thickly covered with silvery pubescence; the front
and vertex almost bare, sparsely punctured ; the eyes almost
parallel ; the ocelli in pits; the front with a shallow central
furrow ; antennal tubercle large, the apex triangular, its
sides distinctly margined, the middle depressed ; below this
is a larger broader one, roundly incised at the apex, the sides
rounded. Pro- and mesothorax shining, sparsely covered
with white hair; the mesonotum distinctly but not closely
punctured ; the scutellums with a few fine punctures. Area
on the base of metanotum narrow, elongate, and marked
with stout striz; the central furrow is wide and deep,
becoming slightly wider towards the apex, and marked with
a few stout striz; on either side of it at the apex is a large
leaf-like expansion, its apex transverse, on the outer side
covered with long hair; at its base is a small rounded pro-
jection. Pro- and mesopleure finely and sparsely punctured ;
below the mesopleural tubercles is a wide, deep, slightly
oblique furrow, marked with some transverse keels; there
is a smooth furrow near the base of the metapleure; the
apex of the latter is rugose and is marked with some trans-
verse keels.
Comes near to P. rufiventris, but is quite distinct
therefrom.
220 Mr. P. Cameron on new
Ichneumonidz.
Suvalta annulipes, sp. 0.
Agrees with S. levifrons in having the front and vertex
smooth, but is smaller, has two yellow marks on the meso-
notum, the scutellum yellow from base to apex, not yellow
on the basal half only; the mark on the mesopleure is
smaller, and there is none on the metapleure ; the black on
hind femora broader, reaching to the middle; the hind coxee
are yellow at the base, not broadly in the middle, and the
hind trochanters yellow, not black.
The ninth to twenty-second joints of antenne yellowish
white below; the flagellum thickly covered with black short
hair ; scape shining, sparsely pilose. Face, clypeus (except
at apex), labrum, mandibles, palpi, apical two thirds of
scutellum, a large somewhat triangular mark on the sides of
the first abdominal segment at the apex, the other segments
broadly at the sides, and the apical almost entirely, yellow.
Four front legs fulvous, yellow at the base, the end joint of
tarsi black ; hind coxe black, with a large yellow band on
the base above; the trochanters and basal half of femora
fulvous, the apical half of femora and of the tibiz black, the
basal half of the tibiz and of the tarsi yellowish. ?.
Length 12 mm.
Had. Khasia Hills. Coll. Rothney.
Face strongly punctured above, in the middle transversely
striated ; apex of clypeus smooth, the base punctured ;
mandibles punctured at the base. Front and vertex smooth
and shining, sparsely covered with long black hair; the
space between the hind ocelli with large deep punctures.
Mesonotum rugosely punctured, reticulated in parts. Scu-
tellum covered with long fuscous hair, its yellow mark is
rounded before and behind, its sides coarsely punctured, the
depressions stoutly striated behind. In the centre of the
metanotum at the base is an area wider than long and having
inside a few stout oblique keels ; the rest of the basal region
reticulated, the reticulations wider on the inner side; the
rest is strongly closely reticulated; the teeth large, broad,
rounded at the top, looked at from behind. Propleurz
sharply margined at the base above, above strongly punc-
tured ; the rest stoutly striated. Mesopleure stoutly longi-
tudinally striated, except in the middle behind ; immediately
under the tubercles the striz are vertical or oblique ; near
the base under the tubercles is a keel. Metapleurz coarsely
rugosely punctured, the punctures running into reticulations.
Hymenoptera from Northern India. 221
Areolet almost square, the recurrent nervure received near
the apical third. Abdomen short; petiole shining, strongly
punctured ; between the apex and the middle are scattered
punctures ; the second and third segments are closely punc-
tured, the others smooth; gastroceeli smooth, hardly de-
pressed in the middle.
Suvalta pallidinerva, sp. u.
Agrees closely in coloration with S. annulipes, but may be
known from it by the longer, more slender petiole, which is
not so much dilated at the apex nor so strongly punctured ;
the head is wider compared with the mesothorax, and the
pronotum is much more dilated at the base, it being there
distinctly tuberculate.
Length to apex of petiole 7 mm.
Hab. Khasia Hills. Coll. Rothney.
Black; clypeus (except at apex), palpi, the inner orbits to
near the end of the vertex, the outer more broadly from near
the top, edge of pronotum (broadly in front, more narrowly
behind), scutellum broadly in the middle, a broad line on
the sides of median segment from shortly above the spines,
a large mark on the base of propleure (broad above, gradually
narrowed towards the apex), the tubercles, a large mark on
the lower side of the base of mesopleurz (curved and nar-
rowed above), the base and lower side straight, a mark under
the hind wings, the greater part of the lateral scutellar keels,
and the sides of the abdominal segments broadly, yellow.
Four front legs fulvous, their coxe and trochanters pallid
yellow ; the fore feuora lined with black above ; the hinder
legs are of a deeper fulvous tint; the cox, trochanters,
shghtly more than the apical third of the femora, apical
fourth of tibiz, the spurs, and base of metatarsus black ; the
tarsi are of a more yellowish tint than the tibie. Wings
hyaline, the nervures, stigma, and costa pale testaceous ; the
areolet is of equal width throughout, a little longer than
broad, the recurrent nervure is received in its apical third.
Mesonotum rugosely punctured, the punctures running
into striations in the middle. Scutellum covered with long
fuscous hair, smooth ; postscutellum very smooth and shining,
The depression in the middle of median segment is smooth,
at its sides it is finely punctured, the outer part coarsely
punctured. The segment outside the keel is coarsely rugosely
punctured; the teeth broadly rounded at the top, oblique at
the sides ; behind them are some curved keels. The upper-
side of the pronotum is roundly incised in the centre, the
pay ay Mr. P. Cameron on new
sides of the propleure above are strongly punctured, the
middle strongly obliquely striated. Mesopleure longitu-
dinally striated (except on the lower side at the base, which
is punctured, and a small smooth space in the middle
behind) ; the tubercles are punctured. Metapleurz closely
rugosely punctured, above more closely punctured. Meso-
sternum punctured, its furrow triangularly widened at the
apex. Petiole shining; before its apex is a punctured band,
surrounding a smooth space; the second and third segments
are closely punctured ; gastrocceli shallow, coarsely acicu-
lated, the part behind them is raised on the outer side and
is very smooth and shining.
The antennz and the apical abdominal segments are
broken off.
Algathia rufopetiolata, sp. n.
Black ; the scape of antennz rufous below, the base of
flagellum brownish, joints 11-14 white below; a triangular
yellowish mark in the centre of the face above; apex of
mandibles testaceous; palpi pale yellow; scutellums, the
sides of the apex of median segment, the apices of the second,
third, fifth, and the whole of the apical abdominal segments
pale yellow ; the petiole rufous, its apex yellow. Legs red;
the four front cox and trochanters pale yellow; the femora
and tibiz fulvous, the tibizw paler, the fore tarsi fuscous
except at the base, the middle blackish; the hinder coxe,
trochanters, and femora rufous; a large mark on the cox
below at the apex, the apex of femora, and tibiz (except a
small dull rufous band at the base) black ; the calcaria pale ;
tarsi black, with rufous spines. Wings hyaline, with a slight
fuscous tinge, the nervures and stigma black ; areolet nar-
rowed in front; transverse median nervure received shortly
in front of the transverse basal. ¢.
Length 8-9 mm.
Hab. Khasia Hills. Coll. Rothney.
Face sparsely punctured laterally, more thickly in the
centre; clypeus punctured, more sparsely below; labrum
fringed with long fulvous hair; the face thickly covered
with fuscous pubescence. Front sparsely punctured, the
inner orbits above sharply margined. Mesonotum closely
punctured, the apex in the middle broadly longitudinally
striated, almost reticulated; middle lobe raised at the base.
Scutellum roundly raised, smooth, covered with long pale
hair. Postscutellum bifoveate at the base. Metanotum at
the base with large deep punctures ; the areola longer than
Ilymenoptera from Northern India. 223
broad, rounded at the base, gradually narrowed to the apex ;
the rounded basal part has a stout central keel and a less
distinct one at the apex ; the lateral arez stoutly obliquely
striated; the posterior median strongly, closely, transversely
striated, the sides more sparsely and strongly. Base of
propleurz aciculated, the upper half strongly punctured, the
lower with some stout striations; meso- and metapleurze
closely and strongly punctured, the latter more strongly and
rugosely above the keel. ‘The postpetiole has a depression in
the middle, which is wide at the apex, narrowed towards the
base ; the second and third segments closely punctured, the
base of the second closely and strongly longitudinally
striated, the striz going on to the gastroceli, which are
shallow, brownish, and aciculated at the apex.
Algathia tibialis, sp. n.
Black ; a mark in the middle of the face above and the
base of the mandibles rufous ; palpi lemon-yellow, the apical
lateral are of the mesonotum except at the base yellow;
first abdominal segment blood-coloured, the sides in the
middle blackish, the apex yellow, the apex of the second,
the sides of the third broadly at the apex, and the sixth and
seventh entirely, pale yellow ; the basal three joints of the
antenne rufous beneath, the tenth to sixteenth white,
fuscous above; four front legs rufo-fulvous, the coxe and
trochanters yellow ; the middle tarsi fuscous; the hind legs
rufous, the apex of the femora, tibie (except at the base),
and the tarsi black. Wings hyaline, with a slight fulvous
tinge, the stigma fuscous. 9°.
Length 8-9 mm.
Hab. Khasia Hills. Coll. Rothney.
Face closely punctured, thickly covered with fuscous
hair, the clypeus more strongly and sparsely punctured, the
front and vertex shining, sparsely punctured, the former
indistinctly keeled. Mesonotum strongly punctured, longi-
tudinally striated in the middle towards the apex. Scutellum
shining, thickly covered with long fuscous hair. Areola
obliquely narrowed towards the base and to a less extent
towards the apex, which is transverse ; its base has a central
and a less distinct and more irregular longitudinal keel on
the sides, the middle irregularly transversely striated; the
posterior median area is (except at the base) transversely
striated ; the outer basal area coarsely punctured, smooth
at the base; the apical stoutly transversely striated, more
stoutly on the apical than on the basal half; spiracular
224 Mr. P. Cameron on new
area finely rugose at the base, more coarsely transversely
rugose before the spiracles, the middle with some stout
curved keels, the apex much more closely but not quite
so sharply obliquely striated. Mesopleure closely punc-
tured, strongly irregularly striated under the tubercles; the
metapleure uniformly, somewhat strongly punctured and
deeply depressed at the base above. Postpetiole obscurely
punctured laterally and furrowed in the middle. Scutellum
thickly covered with long fuscous hair; postpetiole striated
at the base.
Agrees closely in coloration with A. rufopetiolata, includ-
ing the rufous petiole; may be known from it by the
narrower areola, which receives the keel in the middle,
while in rufopetiolata it is received clearly above the middle.
Algathia latibalieata, sp. n.
Agrees closely in coloration with A. zonata; may be
known from it by the black hind coxee, by the base of meta-
notum being rugosely punctured, by the areola being rounded
at the base and stoutly transversely striated, &c.
Black ; a small mark on the face below the antennz
(broad at base, gradually narrowed to the apex, as long as it
is wide at the base), palpi, tegulz, scutellums (except the
scutellum at the base), the apex of the first abdominal
segment, of the second and third more broadly, the apical
two thirds of the penultimate, and the whole of the last, pale
yellow. Mandibles black, the apical third rufous. Palpi
pale yellow. Four front legs fulvous, the tarsi infuscated,
the coxze and trochanters pale yellow; the hind coxe black,
the top and more or less of the inner side rufous; basal joint
of trochanters rufous, apical yellowish ; the femora with the
apex broadly black, the black more extended above; tibize
and tarsi black, the former broadly rufous at the base;
calcaria pale. Wings hyaline, with a fulvous tinge; nervures
fuscous, darker at the base; areolet much narrowed in
front ; the second transverse cubital nervure faint.
Length 11 mm,
Hab. Khasia Hills. Coll. Rothney.
Scape of antennz testaceous in the middle below; the
flagellum at the base obscure brownish, thickly covered with
black hair. Face and clypeus with widely separated punc-
tures and covered with long fuscous hair. Front and vertex
shining, sparsely haired and punctured; the front ocellus
surrounded by a furrow. Mesonotum shining, punctured in
the middle, at the base of the basal lobe almost striated.
Hymenoptera from Northern India. 225
The basal lateral arez of metanotum strongly punctured and
with a curved furrow on the inner side; areola twice longer
than wide, bulging out obliquely in the middle and with the
apex wider than the base and transverse; its basal half is
furrowed deeply down the middle, the sides irregularly trans-
versely striated ; the base of the posterior median area with
a stout longitudinal keel in the middle, the rest transversely
irregularly striated, the strize weaker and closer towards the
apex; the outer arez strongly punctured, the punctures large
and deep, the spiracular area irregularly reticulated at the
base, the rest strongly transversely striated. Propleurz above
with large deep punctures, the depressed middle stoutly,
obliquely, irregularly striated. Mesopleurz strongly punc-
tured, rugosely near the tubercles; the metapleure between
the keels strongly and uniformly punctured. The first ab-
dominal segment smooth, the sides of postpetiole depressed
and punctured ; the middle with a large deep depression ; the
second and third segments closely punctured, the base of the
second closely longitudinally striated; the gastrocceli shallow,
closely striated (except at the apex); the apical segments
thickly covered with white hair.
Algathia rufipes, sp. n.
Black ; the tenth to fifteenth joints of antenne white
below ; face, clypeus, inner orbits and the outer from near
the top, mandibles at the base, palpi, edge of pronotum
(except at the base) narrowly, an irregular squarish mark
behind the middle of the mesonotum, scutellums, sides of
metanotum broadly, the lower edge of propleure, tubercles,
an irregular mark (narrowed in the middle) on the lower
part of mesopleure, a short line below the hind wings, a
small mark over the hind coxe, the centre and apex of
scutellum, the apices of the first, second, third, and fourth
abdominal segments, of the sixth, and the whole of the apical
segment, yellow. Legs rufous, the four front coxe and
trochanters yellow; the hind cox and base of trochanters
black; the hind tarsi white, the basal and apical joints
black. Wings hyaline, the stigma testaceous, the nervures
blackish; areolet narrowed above, the nervures almost
touching there ; transverse median postfurcal. 2.
Length 10, terebra 1 mm.
Hab. Khasia Hills. Coll. Rothney.
Face closely punctured and covered with silvery pubes-
cence ; there is an irregular diamond-shaped mark in its
centre and a less distinct black line above the clypeal foveze.
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 15
226 Mr. P. Cameron on new
Clypeus punctured, but not strongly or closely, its apex
slightly bent inwardly. Scutellum opaque, closely and
uniformly punctured, more strongly than the mesonotum.
Metanotum closely punctured (except in the centre at the
base) ; areola longer than broad and of nearly equal width ;
the teeth broad, large, rounded, and narrowed at the apex.
Propleuree have a plumbeous hue and are irregularly striated
at the apex ; the meso- closely, the metapleure if anything
still more closely, punctured, the punctuation running into
strie at the apex. The second to fifth abdominal segments
are closely punctured ; the gastrocceli striated at the base ;
the petiole is aciculated in the middle towards the apex.
Algathia erythropoda, sp. n.
Black ; the face, clypeus in the centre above, the mark
rounded at the apex, the basal half of the mandibles, palpi,
the inner orbits, the line dilated in front of the ocelli, a line
on the pronotum (broad at the base, gradually narrowed to -
the apex), basal half of tegule, tubercles, scutellum (except
at the base), postscutellum, the fifth abdominal segment
(narrowly in the middle), the apical two thirds of the sixth
and seventh entirely, yellow. Scape of antennz yellow
below, thickly covered with white hair ; the joints of flagellum
dilated below (especially near the apex) and brownish. Legs
rufous, the front coxz and trochanters yellow, the middle
cox yellow, broadly black at the base behind ; the hinder
black, with the apical half yellow above; the basal joint of
the trochanters, apex of hinder tibiz, and the hind tarsi
black ; the spurs pale fulvous. Wings not very clear hyaline,
the stigma and nervures black; areolet narrowed in front,
being there less in length than the space bounded by the
recurrent and second transverse cubital nervures. <6.
Length 1] mm.
Hab. Khasia Hills. Coll. Rothney.
Face coarsely punctured, thickly covered with short white
hair ; the clypeus less strongly punctured, almost smooth at
the apex ; the vertex strongly punctured, the front smooth.
Mesonotum closely strongly punctured. Scutellum shining,
covered with long fuscous hair. Areola broader than long,
the sides at the base obliquely truncated, the apex slightly
bent inwardly, the sides distinctly depressed, with two or
three keels at the apex; the centre raised, rugosely punc-
tured ; the posterior median area widened at the base, closely,
strongly, transversely striated ; the lateral basal arez coarsely
aciculated on the inner side, the rest strongly irregularly
ITymenoptera from Northern India, 227
striated ; the spiracular area behind strongly aciculated, the
rest coarsely transversely striated; the other basal arez
strongly but not closely punctured; the apical areze smooth
at the base, the rest with stout, clearly separated, transverse
keels. Upper part of propleurz strongly punctured, the base
aciculated, the middle below stoutly striated ; mesopleurze
strongly punctured, the base above and the apex below
striated ; metapleurz punctured strongly all over. Post-
petiole strongly and closely punctured, raised in the middle
and obliquely narrowed at the apex; the second and third
abdominal segments closely punctured, the apical thickly
covered with fulvous hair; the gastroceeli large, the base on
the inner side with a stout keel, the outer with two keels.
Comes near to A. parvimaculata ; it is larger, wants the
white bands on the postpetiole, the hinder trochanters are
yellow, not black ; the black mark on the face and elypeus
is much smaller and the middle coxe are yellow.
Algathia varipes, sp. n.
Black; the face, clypeus, labrum, the inner orbits from
the middle of the ocelli to the white face, an oblique some-
what triangular mark near the eyes opposite the hinder
ocelli, the lower three fourths of the outer orbits (the mark
narrow above, broader below), palpi, mandibles (except their
teeth), a line on the pronotum (curved at the base), scutel-
lums, the posterior intermedian, the apex of spiracular end
of the tooth-bearing arez of median segment, a mark above
the hind coxe, the apices of the first and second abdominal
segments broadly (the lines dilated in the middle), the sixth
slightly in the middle, and the whole of the last segment pale
yellow ; the four front legs fulvous, the coxe and trochanters
pale yellow; the hinder coxze black, broadly yellow in the
middle above; the basal joint of the trochanters yellow, the
apical joint and the base of femora rufous, the rest of the
femora, almost the apical half of the tibiz, and the base of
metatarsus black ; the rest of tarsi white, the hinder spurs
dark rufous. Wings hyaline, the costa, stigma, and nervures
black. do.
Length 9 mm.
Hab. Khasia Hills. Coll. Rothney.
Antennal scape beneath and the fourteenth to twenty-fifth
joints white ; scape thickly covered with long fuscous hair,
the flagellum with short black pubescence. Face, clypeus,
and vertex closely and strongly punctured, thickly covered
with short fuscous hair. Mesonotum closely punctured,
15*
228 Mr. P. Cameron on new
opaque; scutcllums shining, smooth, sparsely covered with
short fuscous hair; the basal scutellar keel stout, sharp,
white at the apex, and extending to the middle. Base of
median segment depressed at the base, the furrow smooth,
slightly curved, petiolar area open at the base, areola longer
than broad, rounded at the base, rounded inwardly at the
apex ; posterior median area slightly widened at the base,
almost smooth, only obscurely transversely striated; the
supra- external area has some scattered punctures, the tooth-
bearing coarsely punctured, the spiracular finely punctured
at the base, the rest obliquely striated; the posterior inter-
median coarsely obliquely striated; the teeth indistinct.
Propleurz punctured above, below smooth, the apex in the
middle with some stout punctures ; mesopleure closely
punctured, the metapleure more strongly, with the punc-
tures somewhat more widely separated.
Algathia Rothneyt, sp. n.
Agrees closely in coloration with A. varipes, except that
it has a yellow mark on the mesopieura; otherwise differing
in having the base of the metanotum opaque and aciculated,
the keels bordering the petiolar area are longer, the areola is
not smooth, the teeth are more distinct, the hinder femora
have only the apical third black, and the scutellar keels reach
to the apex.
Black; the head below the antennz, mandibles (except
the teeth), palpi, the inner orbits above, the line narrowed
below, the apical three fourths of outer orbits, edge of pro-
notum (the basal half of the line dilated and acute at the
base), the tubercles, a mark on the hinder edge of meso-
pleurze (longer than wide and obliquely truncated at the
apex), scutellums, the sides of the median segment (broadly
at the apex), a narrow band on the first abdominal segment
(roundly dilated in the middle), the apex of second broadly,
and the apical two entirely, pale yellow. Four front legs
rufous, their coxz and trochanters pallid yellow ; hinder legs
of a deeper red ; coxee black, yellow above and within, the
basal joint of trochanters yellow ; the apical third of femora
and of the tibiz and the basal two thirds of metatarsus
black ; the rest of the tarsi pale yellow, except the apex of
the last jot. Wings clear hyaline, the stigma testaceous,
nervures fuscous. ¢.
Length 8 mm.
Hab. Khasia Hills. Coll. Rothney.
Scape below and joints 9-16 of antenne white, the
Llymenoptera from Nerthern India. 229
flagellum at base and apex brownish beneath. Face closely,
the clypeus more sparsely punctured ; palpi pale yellow ;
labrnm fringed with long fuscous hair. Vertex below the
ocelli closely transversely punctured; front smooth and
shining. Mesonotum closely punctured. Scutellum not dis-
tinctly depressed at base and apex, its keels sharpand extending
to the base of the apical third and depressed on the inner
side ; scutellum bifoveate at the base. Basal area of meta-
notum large, aciculated, obliquely narrowed towards the
apex ; areola nearly as long as wide, the sides at the base
obliquely narrowed, its apex slightly roundly turned in-
wardly ; posterior median area smooth, of uniform width
and rounded at the base; the other are closely punctured,
opaque; the spiracular and the tooth-bearing aree more
strongly, irregularly, and not so closely striated. Propleure
above closely punctured, the apex broadly, in the middle
longitudinally striated ; the base with a broad yellow band,
broader than the upper one on the pronotum ; mesopleurse
closely punctured, the middle-behind coarsely aciculated, the
metapleurz at the base aciculated, the rest closely obliquely
aciculated. Gastrocceli shallow, striated; the base rufous,
striated.
Algathia robusta, sp. n.
Is very similar in form and coloration to A. maculiceps ;
may be known from it by the yellow scutellum, by the
strongly striated front and vertex, by the areola being dis-
tietly defined and the posterior median area not at all,
and by the apex of the hind tibiz and the metatarsus being
black.
Black ; face (except a small black mark above), clypeus,
mandibles, palpi, the inner orbits to beyond the hinder
ocelh, the lower outer orbits (narrowly above, broadly
below), palpi, a narrow line on the pronotum (not reaching
to the base), tegule, a line on the base of the propleure, the
line dilated at the base, two short marks in the centre of the
mesonotum, scutellums, two broad lines on the sides of
median segment, the tubercles, lower part of mesopleurz
(the yellow dilated upwards at the base), the base of meso-
sternum, the apices of the first to fourth abdominal segments,
and the apical entirely, yellow. Four front Jegs fulvous,
tinged with yellow, the apices of the tarsi black ; hinder
coxze and basal joint of trochanters, apex of femora, of the
tibize aud the metatarsus, black; on the apex of the hind
coxie behind is a large yellow mark, narrowed behind.
Wings hyaline, the nervures and stigma pale testaceous ; the
230 Mr. P. Cameron on new
areolet slightly oblique, narrowed in front, the nervures
almost uniting there. <¢.
Length 11 mm.
Hab. Khasia Hills. Coll. Rothney.
Face closely and strongly punctured, its middle above
almost transversely striated ; clypeus less strongly punctured,
its apex smooth; it is thickly covered with short white, the
labrum fringed with long fulvous, hair. Vertex near the
eyes punctured, the centre with three keels, running from
the hinder ocelli, which turn outwardly to the central
furrow, the front finely transversely striated. Mesonotum
closely and strongly punctured. Scutellum at base rugosely
punctured, the rounded apex closely longitudinally striated ;
the keels large, black, and reaching to the apical third.
Middle of metanotum at base with an oblique slope, the sides
margined, very smooth and shining; areola somewhat wider
than long, the base rounded, apex transverse, it is irregu-
larly longitudinally rugose, the middle keeled; the lateral
are rugose, in the centre almost reticulated; teeth large,
wide. Propleurz obscurely punctured above; the meso-
pleurze strongly punctured, the middle slightly, the apex
more strongly longitudinally striated ; the metapleurz with
the spiracular area closely obliquely striated. Postpetiole
closely, finely, irregularly striated, the other abdominal
segments closely punctured ; gastrocceli deep, finely striated
at the base; apex aciculated.
Algathia flavo-balteata, sp. n.
Agrees in size and colour with A. robusta; may easily be
separated from it by the form of the scutellum, which has a
much sharper oblique slope, by the postscutellum being only
obscurely, not strongly striated at the base, by the base of
metanotum being aciculated, by the areola being longer
compared with its breadth, by the black on the hind femora
and tibiw being less extended, by the hind coxz being almost
entirely yellow above, and by the less distinct curve on the
apex of clypeus.
Joints 9-15 of antenne below, the face and clypeus (except
for a small oval mark below the antennez), mandibles, palpi,
inner eye-orbits, the outer from near the top more broadly,
white. A narrow line on the pronotum, tegule, a large mark
near the apex of mesonotum, scutellums, two broad curved
lines on the sides of median segment at the apex, a broad
line on the lower side of the propleurze, a broader one (curved
upwards at the base on the lower side of the mesopleure), a
Hymenoptera from Northern India. 931
narrower one on the hinder edge, a mark below the hind
wings, the basal four abdominal segments at the apex, and
the apical two entirely, whitish yellow. Four front legs
fulvous ; the cox and trochanters yellow; the hind cox
black, the middle above broadly yellow, and there is an elon-
gated mark on the side at the base; the hind femora and
tibiz rufous, as are also the trochanters; the hinder knees,
apex of tibie, and metatarsus black, the rest of the tarsi
white. Wings hyaline, with a slight fuscous tint; stigma
testaceous. ?.
Length 11 mm.
Hab. Khasia Hills. Coll. Rothney.
Face closely and strongly punctured ; the clypeus sparsely
punctured, its apex transverse; the black part of vertex
strongly aciculated, the front strongly trausversely striated
and furrowed down the centre. Propleure with a plumbeous
hue; the meso- closely, the metapleure if anything more
strongly, punctured. Scutellum strongly but not closely
punctured. Median segment closely punctured ; the apex
in the centre closely, at the sides much more strongly,
transversely striated; the teeth large; areola longer than
broad, rounded at the base, slightly narrowed at the apex,
which is transverse. Postpetiole shagreened or finely
striated in the middle; the gastrocceli large, wide, the base
finely striated.
Alyathia femorata, sp. n.
Black ; a mark (elongated and rounded at*the apex) in the
centre of the face above, palpi, scutellum, the outer are on
the apex of the median segment, tlie middle of the tubercles,
the apex of the first and second abdominal sezments, a large
triangular mark on the sides of the third, the apex of the
penultimate, and the whole of the last segment yellow.
Scape of antenne rufous beneath, the middle of flagellum
broadly white. Four front legs fulvous, their coxe and
trochanters yellowish white; the middle tarsi and the hind
legs black, except the trochanters, which are yellow, and the
extreme apex of the femora, which is rufous; the calcaria
white. Wings hyaline, the nervures and stigma black. ?.
Length 10 mm.
Hab. Khasia Hills. Coll. Rothney.
Face strongly, clypeus sparsely punctured. Mesonotum
closely and strongly punctured, thickly covered with short
thick hair. Scutellum smooth, shining. Areola elongate,
the base distinctly, the apex slightly narrowed; the lateral
keels received in front of its middle ; posterior median area
232 On new Hymenoptera from Northern India.
aciculated, shagreened towards the apex; the lateral arew
with some rough transverse keels, the spiracular closely
punctured, the apex raised on the inner side, transversely
striated; the outer two basal arez are closely but not
strongly punctured, the outer apical have three stout, curved,
transverse keels on the apex. ‘The apex of the median seg-
ment is thickly covered with long soft white hair. Propleure
coarsely punctured more finely at the base, the middle below
obscurely striated. Mesopleurz coarsely punctured, below
the tubercles obliquely striated ; metapleure punctured like
the mesopleure. First segment of abdomen smooth, the
depressed sides of the apex punctured; the second and third
segments closely punctured, the base of the second striated
laterally ; gastroceeli not depressed, rufous at the apex. The
apical segments of the abdomen are thickly covered with soft
white hair.
Algathia cariniscutis, sp. n.
Black ; the scape of antenne and joints 8-12 underneath,
the face and clypeus (except for a line in the centre of the
former, which gets gradually thicker until it reaches the
clypeal foveze, the clypeus being also black in the centre), and
the labrum white ; the inner orbits broadly to the end of the
eyes, the outer more narrowly on the lower half, maxillary
palpi, lower part of propleurs, the edge of pronotum
(except at the base), tegule, tubercles, scutellums, the apical
half of median segment, a large oblique mark on the meso-
pleurze above the coxze, a smaller one behind the posterior
coxze, one under the hind wings, the apices of the first and
second abdominal segments, a mark on either side of the
third, and the apical two segments, yellow. Legs rufous,
the four front cox and trochanters bright lemon-yellow,
the apices of the tarsi fuscous; the hinder cox black,
broadly yellow above and at the sides above on the inner
side, their middle behind next to the black part rufous ; the
trochanters black, the basal joint for the greater part yellow
above; the apex of the hind femora and the base of the tibi
more narrowly black; the hinder tarsi paler, not so rufous
in tint as the anterior, their apex black. Wings clear
hyaline, the stigma and nervures black. ¢.
Length 8 mm.
Hab. Khasia Hills. Coll. Rothney.
Face and clypeus closely punctured, covered with short
white down; the front and vertex almost impunctate.
Mesonotum closely and uniformly punctured; scutellum
smooth, covered with fuscous pubescence, its sides stoutly
On the Anatomy of Eryx and other Boide. 233
keeled. Areola slightly wider than long, rounded at the
base, the apex bulging inwardly; the base of posterior
median area smooth, the rest transversely striated ; the outer
apical areee are more strongly and widely striated. The
upper half of propleure closely punctured, as are also the
mesopleure ; the metapleurz are more closely and strongly
punctured. First segment of abdomen aciculated, the post-
petiole more strongly and raised in the middle; the second
and third segments are closely punctured; the gastroccell
wide, striated, the oblique apex aciculated.
XXIV.—Preliminary Note on certain Points in the Anatomy
of Kryx and other Boide, partly indicative of their Basal
Losition among the Ophidia. By FRANK EK. BeppDarp,
M.A., F.R.S.
Ir is generally believed that the Boide occupy phylo-
genetically a place at or near the base of the Ophidian series ;
and this view is expressed by Boulenger in a tabular state-
ment of the mutual affinities of the various families of the
Order *. This opinion is largely based upon the persistence
of considerable vestiges of the pelvic girdle and upon the
paired lungs. In studying the anatomy of snakes I have
been able to note a few other points to which little or, in
some cases, no attention has been paid and which tend to
the support of this conclusion. My observations bearing
upon this subject were made upon Python, Eryx, and Boa.
The first point to which I would draw attention is the
equal size of the right and left aortic arches, which join to
form the dorsal aorta. In at least many other snakes (for
example, Zamenis flagelliformis) the right aortic arch is so
much the smaller that it appears almost as an inconspicuous
branch of the left. It would appear, however, that in Python
bivittatus this is not the case fT, though Dr. Gadow’s drawing t¢
ot Pelophilus madagascariensis is in accordance with the facts
which I have observed.
Secondly, the intercostal branches of the aorta are arranged
in a fashion which appears to me to be distinctly archaic.
In most snakes the intercostal arteries are very uregular in
* “Catalogue of the Snakes in the British Museum (Natural History),’
London, 1893, vol. 1. p. 2.
+ Bronn’s ‘ Klassen und Ordnungen des Thierreichs,’ Bd. vi, Abth. iii.
pl. exxxiv. fig. 2. This figure is copied from Fritsch,
t 2bid. pl. cxxxv. fig. 1.
234 Mr. F. IX. Beddard on the
their origins from the dorsal aorta and their points of entrance
into the thickness of the dorsal parietes.
They arise at unequal intervals from the aorta and enter
the parietes at varying distances from each other. In Python
reticulatus, Hopkinson and Pancoat* did not figure these
arteries at all; but Jacquart ft in another python figured
them as single arteries arising regularly from the aorta f.
I do not find this in Python spilotes. But as the conditions
in Eryx are more primitive still, I refer to that snake only
for the present. Here the intercostal arteries are practically
regular in their arrangement, being metamerically disposed
in agreement with the vertebra. There is a pair to each
intervertebral interval. The two arteries of the pair either
arise side by side from the aorta, or an artery single in its
origin soon bifureates. I cannot but think that this arrange-
ment of the intercostals is more primitive than that which
is more usual among the Ophidia. I may remark that it
ceeurs in the Lacertilia (e. g. Chameleon, Tiliqua, &c.).
I am uncertain whether to regard the total absence of a
gubernaculum, tying down the ventricle to the pericardium,
as indicative of a primitive structural relationship. It may
at first appear unnecessary to record the fact of the absence
of a gubernaculum. For it is generally stated § that the
Ophidia are to be contrasted with the Lacertilia in this very
point—the Lacertilia possessing a gubernaculum and the
Ophidia being deprived of one. I find, however, considerable
vestiges of this tag” in certain Ophidia, but not in Eryx
or Boa. On the other hand, I think it may be regarded as
probable that a conspicuous azygos vein is a_ primitive
feature. Now in Python spilotes this vein collects blood
from and therefore extends over many more than four inter-
costal spaces, which is the limit of this vessel in Corone/la
getula. In Eryex conicus the azygos vein collects blood from
no less than ten intercostal spaces.
As a general rule a considerable number of renal arteries
(even as many as eight in Coluber catentfer) supply each
kidney. This is correlated with the considerable length of
the gland in most snakes; I cannot, however, ascertain that
there is an exact relationship between the length of the
kidney and the number of arteries supplying it. But the
* Trans. Amer. Phil. Soc. v. 1837, p. 121.
+ Ann. Sci. Nat. (4) iv. p. 321.
{ In Python Sebe | find an identical arrangement. The arteries aise
singly and bifurcate just before entering the parietes.
§ For instance, in that section of Bronn’s ‘ Klassen und Ordnungen des
Thierreichs’ which deals with snakes.
Anatomy of Eryx and other Boide. 235
existence of only a single renal artery on each side in some
Boidze, though doubtless associated with a small kidney *, is
of itself, as it appears to me, a primitive character, inasmuch
as there is here an absence of reduplication, so common a
feature of the vascular and other systems in the Ophidia.
The same arguments may be used in the case of the gastric
arteries, which are two in £ryz and three in Python spilotes.
In the genus Coluber there may be as many as ten or eleven
gastric arteries.
It is not common in snakes, so far as my experience goes,
for the two carotids at their origin to be equal in size: they
are, however, in both Myx jaculus and EH. conicus, but not
in Python spilotes. Another primitive (?) feature which is
found in only one of the two genera mentioned is connected
with the dorsal musculature of Python spilotes. As a general
rule, in snakes a beautiful complex of tendons is seen to
occupy the dorsal median region when the animal is opened
from below. In Python this region is much less converted
into tendon; it remains muscular. Now there is evidence
elsewhere in the animal kingdom of muscles becoming more
tendinous or being converted entirely into ligaments, but not
of ligaments and tendons acquiring a muscular character +.
Some features in the circulatory system, other than those
briefly referred to above, are not without interest.
It isat least rare among snakes { for the arteries supplying
the gonads to arise from the aorta opposite to each other
instead of one being in front of the other. Nevertheless, in
a female Hryx conicus the ovarian arteries form a pair arising
side by side. As is usual, these arteries immediately follow
the superior mesenteric.
It is a peculiarity of snakes, contrasted with lizards, that
the anterior abdominal vein of the latter is single, while it is
at least sometimes partly double in the Ophidia. T'his point
of difference from the Lacertilia, and, so far, of resemblance
to the Crocodilia, is apt to be slurred over in text-books. In
one specimen of Hrya conicus the vessel was single through-
out; in another it was partly double, as was the case with
two specimens of Hrya jaculus. In Boa constrictor the vessel
was single for a distance of six inches behind the gall- bladder
and thence to the cloaca double.
* In Heterodon platyrhinus, for example, the proportions between the
length of the body (to the vent) and the length of the larger kidney are
9:1, in Boa constrictor 15:1.
+ For example, one of the glutzeal muscles in hornbills.
{ I have not myself observed a single instance, except in the case
mentioned above.
236 On a new Genus of Spatangoids.
In Python Sebe the fluctuation of this vein between the
single and double condition was more plainly seen. Just in
front of the gall-bladder the vessel communicates with the
‘astric portal vein ; from this point to two inches behind the
gall-bladder it is single. For a distance of 44 inches it is
formed of two tubes lying side by side; these then reunite and
finally again separate to form two tubes. This example
shows that the double character of the vein is not only due
to the elongation of the body, and as a consequence the
equivalent of the posterior double region of the same vein in
Lacertilia, where it emerges from the two posteriorly situated
fat-bodies.
XXV.—Deseription of a new Genus of Spatangoids.
By F. Jerrrey Ber, M.A.
Amona@ the Prymnodesmid Spatangoids (or those with a
subanal fasciole) the genera known as Brissus, Meoma, and
Metalia are ordinarily recognized as forming a compact
group. I have lately received from a valued correspondent,
Mr. F. W. Townsend, some specimens from the coast of
Oman which have a striking resemblance to these three, but
are at once distinguished from all of them by the position of
the apex, which is hardly, if at all, excentric, This sub-
central position of the apex suggests that this new form is
phylogenetically older than the three genera to which it seems
to be allied; and I suggest for it, therefore, the name of
Hobrissus.
The genus may be diagnosed in the following terms :—A
Prymnodesmid Spatangoid with the apex almost central and
the anterior ambulacrum flush with the test; the antero-
lateral ambulacra directed forwards and not at right angles
to the long axis of the test; an open circumanal fasciole, as
in Metalia.
The possession of a circumanal fasciole has generally been
regarded as a recent acquisition, so that it is of importance to
note its coexistence with the archaic position of the apex.
Specific characters and name.—As there is but a single
form known, the specific characters must be guessed at. In
general appearance like a small Brissus unicolor, with light-
coloured Brissine spines, none of much greater length than
the rest; those on the abactinal side longer and sharper than
those on the actinal. Larger tubercles scattered among the
smaller on the actinal surface, more regularly larger below ;
the lateral ambulacra moderately wide and slightly sunken.
Four pairs of pores on each side within the subanal fasciole.
bo
bas |
On a new Barbus from Cameroon.
Hab. Indian Sea, off Oman.
The species may well be called, after its finder, Hvbrissus
Townsend?,
The following measurements may be of some service :—
Test. | Length of Ambulacra.
| wii :: is | % |
rs | Greatest | Height at | , ents) : ape
Length. | breadth. | arex. Anterior. | Ant. lat. | Post. lat. |
64 Lo ae ed on re
| | |
D4 44 | 28 22:5 | 21°5 21°5
3) 30 | 21 iff 4 14
XXVI.—Deserip'ion of a new Barbas from Cameroon.
By G. A. Boutencer, F.R.S.
THE number of recently discovered African Barbels of the
group of Barbus Bynni is really surprising, Until a year
ago the group was unrepresented in West Africa; then I
described a species, B. Batesii *, allied to the East-African
B. tanensis, Gthr., discovered in Cameroon by Mr. G. L.
Bates, whilst the description of a second closely allied species,
likewise from Cameroon, B. Linnelli, Lénnberg, appeared in
the last number of these ‘ Annals? f, hanks to the exer-
tions of Mr. Bates, I am now able to add a third Cameroon
species to the list.
Barbus micronema,
Depth of body 3 times in total length, length of head 4 to
4> times. Snout rounded-subtruncate, 23 to 3 times in
length of head, projecting beyond the mouth, with small
pearl-like granules on the sides ; diameter of eye 42 to 54
times in length of head, interorbital width twice to twice and
one third ; mouth inferior, forming a broken arch, a feebly
curved transverse line in front, its width 3 times in length of
head ; lips feebly developed, lower restricted to the sides ;
edge of lower jaw forming a blunt keel; barbels one or two
on each side, the anterior, if present, quite minute, the poste-
rior } diameter of eye. Dorsal III 10, last simple ray strong,
bony, not serrated, its rigid part 2 to 2 length of head, free
edge of the fin strongly emarginate ; its distance from the
occiput a little less than its distance from the caudal fin,
* Proe. Zool. Soc. 1903, i. p- 29, pl. ii. fie, 2.
T P. 138.
238 Structure of the Teeth of some Potsonous Snakes.
Anal III 5, longest ray # length of head, reaching root of
caudal. Pectoral as long as or a little shorter than head, not
reaching ventral; latter below middle of base of dorsal.
Caudal fin deeply forked, upper lobe pointed and much longer
than lower. Caudal peduncle slightly longer than deep.
Scales 27 Z, 2 between lateral line and ventral, 12 round
caudal peduncle. Olive-brown above, golden below, the
scales darker at the base ; fins dark.
Total length 340 mm.
Two specimens from the Kribi River.
This species must be placed near B. perplexicans, Bler.,
from the Tana River, EH. Africa; like that species and the
Abyssinian B. plagiostomus, Blgr., the shape of the mouth
approximates it to the species of Varicorhinus or Capoéta ;
whilst in the condition of its barbels it serves to connect the
species with two pairs of barbels with those with a single pair.
XXVII.—WNotes on the Structure of the Teeth of some
Poisonous Snakes found in Travancore. By R. SHUNKARA
NARAYANA PILLAY.
In offering the following notes on the structure of the teeth
of the poisonous Colubrine snakes I do not aspire to lay claim
to originality, as my observations have been based on the
lines of those already made by eminent men, and refer to a
few snakes found in Travancore.
Since April 1901 I have been supplying snake-venom to
the Pasteur Institute of India, Kasauli, and to Messrs. Bur-
roughs, Wellcome, & Co.’s Research Laboratory. I had a
fancy for the study of snakes, and as Preparator to the
Museum I availed myself of the opportunity to make a com-
parative study of the poisonous and non-poisonous snakes, in
the course of which, while examining the skull of a hamadryad
(Nata bungarus) 14 feet long, the skeleton of which was
being articulated for the museum, I noticed a certain pecu-
liarity in the structure of the teeth which, to my mind,
appeared to be abnormal—namely, the presence of grooved
posterior maxillary teeth.
According to Mr. G. A. Boulenger *, the genus Nata is
defined as having the poison-fang followed by one or more solid
teeth ; and in Sir Joseph Fayrer’s ‘ Thanatophidia of India’
mention is made of ‘a second simple tooth at some distance
behind the fang.” Later on I examined a spirit-specimen of
Naia bungarus, and in this, too, I found the posterior maxillary
teeth were grooved, the grooving being shallow or ill-defined
* (The Fauna of British India,’ Reptilia and Batrachia (1890).
Obituary Notice. 239
and invisible to the naked eye. I communicated this to
Mr. H. 8S. Ferguson, the Director of the Museum, and he
informed Mr. G. A. Boulenger, who, while verifying and
confirming the faintly grooved posterior maxillary teeth in the
genus Nava, a discovery * made by him since the publication
of the ‘Fauna of British India,’ does not seem to have been
aware of the more or less grooved palatine series of teeth as well.
At his instance I was led to a series of observations on the teeth
of various poisonous Colubrine snakes of the subfamily
Elapine so far as they are represented in Travancore, and, in
addition, to the grooved functional and reserve fangs.
Posterior
maxillary. Palatine. Pterygoid.
Naia bungarus has ...... 3 Vi 12
tripudians has ...... ul 5 14
Bungarus ceruleus has.... 3 10 15
In the above not only are the posterior maxillary and palatine
teeth more or less grooved, but all the pterygoid and man-
dibular series are likewise marked with faintly depressed
lines resembling grooves. Furthermore, in connexion with
an examination of two skulls of Hemibungarus nigrescens, a
small poisonous Colubrine snake fairly common on the hills,
I found the palatine teeth indistinctly grooved.
Government Museum, Trevandrum,
October 26, 1903.
Obituary Notice: Dr. WILLIAM FRANCIS.
Dr. Wittram Francis was born in London on the 16th of
February, 1817. He was educated at University College School
and St. Omer. He left St. Omer in 1834 and proceeded to
Crefelt, but in the autumn of the same year went to Gera, where
he remained for about two years. In 1836 he returned to England
and spent a year at the London University (University College),
afterwards devoting some time to learning the printing business
under Mr. Richard Taylor, to whom he had been apprenticed some
time previously. He then went to Berlin, and thence to Giessen,
where he studied under Liebig, and did much original work, chiefly
on the salts of molybdenum. He took his degree of Doctor of
Philosophy at Giessen in 1842.
He early developed a taste for Natural History, and during
his stay at Gera he devoted much of his time to entomological study
and pursuits. While in England, in 18387, “ fresh from the teach-
ings of Ehrenberg, and profoundly influenced by the spirit of
scientific research which then, as now, prevailed in Germany,” he
“ suggested to Mr. Richard Taylor the establishment of a journal
in which, while its pages were freely open to the original contri-
* Catalogue of Snakes,’ iii. p, 373 (1896).
2 £0 Obituary Notice.
butions of English naturalists, special attention should be paid to
the researches of Continental observers; and the result was the
starting of the ‘Annals of Natural History,’ with which, sub-
sequently, the well-known ‘Magazine of Natural History’ of
Loudon and Charlesworth was amalgamated.” His name first
appears on the wrapper as co-editor in 1859. As Editor of the
‘Annals’ he became acquainted with most of the leading natu-
ralists, and made many life-long friends, lis indebtedness to whom
he warmly acknowledges in the Preface to the Sixth Series.
While in Berlin and Giessen, Dr. Francis, in conjunction with his
friend and fellow-student Henry Croft, forwarded every month a
series of reports to the ‘Philosophical Magazine’ on the progress of
chemical science on the Continent ; but the space available in that
Journal being limited, they, on their return to England, started
the ‘Chemical Gazette’ in 1842. Croft was compelled to re-
linquish the editorship before the fourth number appeared, being
appointed Professor of Chemistry at King’s College, Toronto ;
and the ‘ Gazette’ was carried on by Dr. Francis alone until 1859,
when the pressure of other work compelled him to relinquish the
task, and the ‘Gazette’ was incorporated with the then newly
founded ‘Chemical News.’
In addition to furnishing translations of foreign scientific
papers to the ‘ Philosophical Magazine,’ he also translated many
papers for Taylor’s ‘Scientific Memoirs,’ in the conducting of
which, moreover, he had a very large share, although his name
did not appear on the titlepage. He also translated Beckmann’s
‘ History of Inventions’ for Bohn’s Scientific Series.
In 1851 his services to the ‘ Philosophical Magazine’ over
many years, both in furnishing translations and in conducting
the Journal, were acknowledged by the appearance of his name
on the wrapper as co-editor, where it remained until his death.
During the whole period of fifty-three years he took an active
part in the management of the Magazine. His acquaintance
and, in many cases, warm personal friendship with scientific
men both in Great Britain and on the Continent, his sound
judgment, and tact made his services in this capacity invaluable.
In 1841 he was elected Associate of the Chemical Society,
becoming a Fellow in the following year. He was also a Fellow
of the Linnean Society (1844), of the Royal Astronomical (1851),
of the Geological (1859), and of the Physical (1876).
In 1852 he joined Mr. Richard Taylor as partner in the firm of
Taylor and Francis, printers and publishers. He was one of the
oldest members of the Stationers’ Company, having taken the
Livery in 1841.
In 1862 he married Isabella Gray, daughter of Mr. Taunton,
M.R.CS., of Hatton Garden, but became a widower in 1899.
For some few years previous to his marriage Dr. Francis had lived
at Richmond, and for the rest of his life continued to reside
ihere—for the last thirty-one years at the Manor House, where
he died on the 19th of January last.
THE ANNALS
AND
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]
No. 76. APRIL 1904.
XXVIII.—Deseriptions of some new Species of Lepidoptera
Heterocera from Tropical South America. By HERBERT
Druce, F.L.S8. &e.
Fam. Syntomida.
Ctenucha albolineata, sp. n.
Male.—Head, antenne, collar, tegule, underside of the
thorax, and legs black ; thorax and abdomen metallic blue,
the anal tuft black. Primaries black, a white line from the
base through the middle of the cell almost to the outer margin
below the apex; above the end of the white line is a small
round white spot; the base and inner margin of the wing are
streaked with metallic blue: secondaries black, with a wide
white band along the costal margin, not quite reaching the
apex; the fringes of both wings black.
Expanse 1? inch.
Hab. N. Peru, Huancabamba, 6000-10,000 feet (Mus.
Druce).
This species is allied to Ctenucha clavia, Druce, from
Keuador,
Fam. Arctiidae.
Automolis dolens, sp. n.
Female-—Head, antenne, thorax, abdomen, and legs
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 16
2492 Mr. H. Drnce on some
black ; collar, tegule, and base of the abdomen yellowish
white. Primaries black; a wide yellowish-white band
crosses the wing near the base from the costal to the inner
margin, the band is slightly widest on the inner margin; a
yellowish-white narrow band crosses from the costal margin
near the apex to the outer margin, then curves down along the
outer margin to the anal angle; the fringe yellowish white :
secondaries black, the basal third of the wing yellowish
white. ‘The underside the same as above.
Expanse 1? inch.
lab. Paraguay (Mus. Druce).
This species is allied to Automolis rectiradia, Hampson,
from the Upper Amazons, also to Automolis tegyra, Druce.
Anaxita Lysandra, sp. n.
Male.—Head, antenne, and legs black, collar brown ;
tegule brown, edged with long black hairs; thorax and
abdomen black, the sides bright red, the underside of the
abdomen with four yellow spots near the base. Primaries
brown, thickly irrorated with yellow scales; three yellow
spots edged with black on the costal margin, the first and
third small, the second long; veins all black, edged with
pale yellowish brown, between each vein a long red line
edged with black; fringe black: secondaries dark brown,
veins black, with bright red streaks between them; the fringe
black. Underside very similar to the upperside ; secondaries
with more red and with a yellowish streak along the costal
margin.
Expanse 38 inches.
Hab. N. Peru, Huancabamba, 6000-10,000 feet (Mus.
Druce).
A very fine species, very distinct.
Fam. Ceratocampide.
Adelocephala nisa, sp. n.
Male.—Head and palpi pink, antenne and tegule yellowish
brown, the latter edged with pink, the thorax and upperside
of the abdomen yellowish brown, the underside of the abdo-
men and legs bright pink. Primaries pink, crossed by a wide
dark yellowish-brown band extending from the apex to the
middle of the inner margin; a white dot at the end of the
cell, edged with pink ; the fringe yellowish brown: second-
aries pinkish brown, darkest along the inner margin; the
fringe pink. The underside whitish pink, the costal half of
new Species of Lepidoptera. 243
the primaries yellowish ; a rather faint black line extends
from the apex almost to the inner margin; a black spot at
the end of the cell; the costal margin of the secondaries
slightly blackish.
Expanse 33 inches.
Hab. Peru, Santo Domingo, 6009 feet (Mus. Druce).
Adelocephala hodeva, sp. n.
Male——Head and antennze dark brown; tegule pinkish
brown; thorax and abdomen above dark brown, tlie sides
of the abdomen banded with white, the underside pinkish
grey; legs greyish brown. Primaries dark brown, the outer
margin greyish brown, in some lights pinkish brown; a very
distinct white spot at the end of the cell; the fringe dark
brown: secondaries dark red, shading to brown along the
inner margin; the fringe greyish brown. Underside: pri-
maries, the costal half of the wing dark brown, the inner
half red, the outer margin greyish; a dark brown line
extends from the apex almost to the middle of the wing:
secondaries pinkish grey, irrorated with small black spots ; a
short brown line extending from the anal angle to about the
middle of the wing.
Expanse 44 inches.
Hab. British Guiana (Mus. Druce).
Adelocephala Eugenia, sp. n.
Female.— Head, antennz, collar, and tegulze brown; thorax
and base of the abdomen citron-yellow, the upperside of the
abdomen brownish yellow ; the anal segment, underside, and
legs dark brown. Primaries dark brown, with a greyish
shade at the base across the middle of the wing and _ partly
along the outer margin ; a small white spot at the end of the
cell: secondaries dark brown, with some yellow hairs at the
base ; the fringe pale brown. ‘The underside of both wings
pale greyish brown.
Expanse + inches.
Hab. French Guiana (Mus. Druce).
Adelocephala Smitht, sp. n.
Male.—Head, antenne, collar, and tegule pale yellowish
brown ; thorax yellow, speckled with brown; abdomen pale
yellow, whitish on the underside. Primaries pale yellow,
thickly irrorated with small brown spots, thickest at the base
of the wing: secondaries pale yellow, with rather a ijarge
16*
214 Mr. H. Druce on some
tuft of red hairs on the inner margin. Underside: primaries
pale greyish brown, irrorated with small brown spots; the
base of the wing red; a black spot at the end of the cell :
secondaries cream-colour, irrorated with minute brown dots.
Expanse 3 inches.
Hab. Colombia, Cacagualito, 1500 feet (H. H. Smith,
Mus. Druce).
Adelocephala yucatana, sp. n.
Female.—Head, collar, tegule, thorax, and abdomen
yellowish brown, antennz and legs brown. Primaries pale
yellowish brown, thickly irrorated with dark brown scales ;
two faint brown lines cross the wing from the costal to the
inner margin, the first nearest to the base, the second beyond
the middle ; an ill-defined brown spot at the end of the cell:
secondaries pink, edged with yellow round the outer margin ;
the fringe of both wings yellow. Underside very similar to
the upperside, but without the lines crossing the primaries
and with a large black spot at the end of the cell ; the costal
margin of the secondaries is also black.
Ixpanse 31 inches.
Hab, Yucatan (Mus. Druce).
Adelocephala Uneata, sp. n.
Male.—Head, antenne, collar, tegule, thorax, and abdo-
men pale yellow, the underside of the abdomen and legs
yellowish white. Primaries pale yellow, the base of the
wing greyish brown; a white dot at the end of the cell,
beyond which a greyish-brown line crosses the wing from
just below the apex to the inner margin close to the base:
secondaries pale chrome-yellow; the fringe of both wings
yellow. ‘The underside of the primaries and secondaries
pale yellowish white.
Iixpanse 2} inches.
Hab. Paraguay (Mus. Druce).
Fam. Saturniide.
Attacus vibidia, sp. n.
Male.—Wead dark brown; collar white, edged with black ;
tegule and thorax brown; abdomen black, each segment
edged with white ; underside of the abdomen and legs brown.
Primaries pale brown, irrorated with black scales ; a curved
white line near the base, edged with black on the outer side ;
a wide hyaline >-shaped mark at the end of the cell, edged
new Species of Lepidoptera. 245
with black on both sides ; a waved black line extending from
the costal margin, beyond which the wing is shaded with
white, brown, and yellow; two large black spots edged with
white on the inner side close to the apex: secondaries pale
brown ; an indistinct greyish line close to the base; a large
hyaline angular-shaped spot edged with black at end of cell,
below which a waved black line, edged with white on the
outer side, extends from the costal margin near the apex to
the inner margin above the anal angle; beyond the black
line the wing is pinkish, then yellowish brown to the outer
margin ; a submarginal row of small black dots extends from
the apex to the inner margin. Underside very similar to the
upperside, but paler in colour.
Expanse 34 inches.
flab. Argentine Republic, Tucuman (Mus. Druce).
A small species, very distinct from any known to me.
I'am. Lasiocampide.
Ormiscodes radama, sp. n.
Male.—Head and underside of the thorax and legs reddish
brown ; antenne, collar, and tegulee chrome-yellow; thorax
reddish brown ; abdomen black, each segment edged with
white, the anal tuft yellowish brown. Primaries, the costal
half of the wing yellow, the inner half clouded with brown,
the veins black ; a <-shaped white mark at the end of the
cell and a white spot beyond ; an indistinct slightly waved
band crosses the wing from near the apex to the middle of
the inner margin ; the fringe alternately white and brown:
secondaries yellowish brown, palest at the base and along the
Inner margin ; a curved brown line crosses the wing beyond
the middle; the veins all black. Underside very similar to
the upperside, except that the white markings on the pri-
maries are much smaller and that the costal margin of the
secondaries is bordered with white.
ixpanse 34 inches.
Hab. 5.H, Peru, Santo Domingo, 6000 feet (Mus. Druce).
Ormiscodes (?) choba, sp. n.
Male.—Head, collar, tegule, thorax, abdomen, and legs
pale pink; antenne yellow. Primaries pink, slightly yellowish
about the middle of the costal margin, and a yellowish line
crossing the wing beyond the cell from the costal to the inner
margin ; two waved black lines extending from the costal to
the imner margin, the first near the base, the second sub-
246 Mr. H. Druce on some
marginal; a black dot at the end of the cell; the fringe
yellowish pink : secondaries bright pink, darkest on the inner
half of the wing. ‘The underside of both wings pale pink,
both wings crossed by two narrow dark pink lines.
Expanse 3 inches.
Hab. §.E. Peru, Santo Domingo, 6000 feet (dus. Druce).
Megalopyge gamelia, sp. n.
Male.—Head, thorax, and abdomen white; collar and tegulz
black ; antenne yellowish. Primaries white, the costal margin
from the base nearly to the apex dark grey ; a black dot close
to the base of the wing; a double row of small black spots
crosses the wing from the apex to the middle of the inner
margin; the fringe alternately black and white: secondaries
white, with a submarginal row of black spots extending from
the apex to theanal angle; the fringe black and white. The
underside of both wings dusky white, without any markings.
Expanse 1? inch.
Hab. 8... Peru, Santo Domingo, 6000 feet (Mus. Druce).
Apatelodes mehida, sp. n.
Male.—Head, antenne, tegula, and abdomen pale greyish
brown; the palpi and thorax black. Primaries greyish brown,
the veins darker brown; a large brown spot, edged with
white, on the outer side close to the apex ; a dark brown
elongated spot on the inner margin near the base ; a straight
brown line crosses the wing from the apex to the anal angle,
between it and the base are two narrow curved lines ex-
tending from the costal to the inner margin: secondaries
reddish brown, crossed about the middle from the costal to
the inner margin by a pale greyish-brown waved band,
darkest on the inner margin. Underside: primaries pale
brown, the dark brown patch at the apex considerably larger,
the lines crossing the wing very indistinct ; secondaries dark
reddish brown, with a very pale brown submarginal line
extending from the costal margin to the anal angle; the
underside of the abdomen dark brown.
Expanse 24 inches.
Hab. 8.E. Peru, Santo Domingo, 6000 feet (Jfus. Druce).
Apatelodes signata, sp. n.
Male.—Head, collar, tegule, thorax, and abdomen brown;
antenne yellowish brown; legs and underside of the abdo-
men dark brown. Primaries dark brown, irorated with
new Species of Lepidoptera. 247
minute greyish scales; a pale brown spot at the end of the
cell; a dark brown curved line crosses the wing beyond the
middle from the costal to the inner margin; a submarginal
greyish curved line extends from the apex to the anal angle:
secondaries dark fawn-colour, crossed below the middle from
the apex to the inner margin by two faint brown lines; the
fringes of both wings brown. Underside: both wings pale
brown, with the dark lines more distinct than on the upper-
side ; a black spot at the end of the cell of the primaries and
secondaries.—Female very similar to the male, but darker in
colour.
Expanse, g 24, 2? 3 inches.
Hab, S.K. Peru, Santo Domingo, 6000 feet (Mus. Druce).
Apatelodes banepa, sp. n.
Male.—Head and thorax black; antenne, collar, and
tegulz pale greyish brown ; abdomen and legs brown. Pri-
maries greyish brown, two small white spots close to the
apex, edged with black on the inner side; a large elongated
dark brown spot close to the base on the inner margin, and
three zigzag indistinct black lines cross the wing from the
costal to the inner margin ; fringe brown: secondaries pale
reddish brown, crossed about the middle by an indistinct
whitish line.
Expanse 2 inches.
Hab. §.K. Peru, Santo Domingo, 6000 feet (AZus. Druce).
Lonomia bethulia, sp. n.
Male.—Head and antennz black; collar, tegule, thorax,
and abdomen reddish brown; legs black. Primaries pale
yellowish brown, crossed near the base from the costal to the
inner margin by two waved, curved, dark brown lines ; three
small black dots at the end of the cell, beyond which a
straight, rather wide, dark brown line crosses the wing from
the costal to the inner margin ; a submarginal, zigzag, fine
brown line extends from the apex to the anal angle : second-
aries pale reddish brown, with a very fine line crossing the
wing about the middle; the fringes of both wings brown.
Underside very similar to the upperside, but paler in colour
and with all the lines very indistinct.
Expanse 24 inches.
Hab. N. Peru, Huancabamba, 6000-10,000 feet (Mus.
Druce).
This species is allied to LZ. monacharia, Mssn.; some
specimens are much darker in colour than others.
248 Mr. FI. Druce on some
Fam. Bombycide.
Hygrochroa intricata, sp. n.
Male.—Head, antenne, collar, tegule, thorax, and abdomen
pale olive-brown. Primaries pale olive-brown, crossed from
the costal to the inner margin by two rather wide dark olive-
brown bands, which are united just below the cell; the base
and the apex of the wing olive-brown; a greyish-white
marking on the outer margin above the anal angle and a
black dot at the end of the cell; the fringe yellowish brown :
secondaries pale yellowish fawn-colour, with some dark
markings on the inner margin.
Expanse 1? inch.
Hab. §.E. Peru, Santo Domingo, 6000 feet (Afus. Druce).
Tam. Notodontide.
Marthula aurea, sp. n.
Male.—Head, palpi, and thorax dark brown; tegule and
abdomen pale fawn-colour; legs and underside of the abdo-
men brown; antennze yellowish brown. Primaries pinkish
brown, becoming golden red along the costal margin ; four
indistinct angular brown lines cross the wing from the costal
to the inner margin; two black lines close to the anal angle:
secondaries white, clouded with black at the anal angle and
round the outer margin; the fringe greyish. Underside:
primaries uniformly blackish brown; secondaries white, the
costal margin pale yellow.
Expanse 2 inches.
Fab. 8.E. Peru, Santo Domingo, 6000 feet (Mus. Druce).
Lustema carama, sp. n.
Male.—Head, collar, tegule, thorax, and abdomen black,
the thorax clothed with long yellowish hairs, underside of the
thorax and legs black; the antenne, anal tuft, and the under-
side of the abdomen yellowish brown. Primaries and second-
aries pale greyish brown, the veins all black ; fringes of both
wings blackish brown. Underside the same as above.
Expanse 23 inches.
Hab. S8.E. Peru, Santo Domingo, 6000 feet (Alus. Druce).
This species is allied to E. dora, Druce, from Mexico,
Heterocampa dolens, sp. n.
Male.—Head, antennee, collar, tegule, thorax, abdomen,
new Species of Lepidoptera. 249
and legs black. Primaries black, thickly irrorated with
white scales; a white zigzag line crosses the wing close to
the base; a large white patch beyond the cell and curved
white line extending from the costal to the inner margin
nearest the anal angle; the fringe alternately black and
white: secondaries white, the costal margin clouded with
black, the marginal line black ; the fringe white. Underside
similar to the upperside, but the primaries not so distinctly
marked.
Expanse 2 inches.
Ilab. 8... Peru, Santo Domingo, 6000 feet (Mus. Druce).
feterocampa longula, sp. n.
Male.—Head, antenne, collar, and tegule reddish brown ;
thorax grey, abdomen dark grey, anal tuft white. Primaries
silvery white, thickly irrorated with reddish-brown scales; a
series of reddish-brown spots close to the apex; a brown spot
at the end of the cell, edged with black; fringe grey:
secondaries white. Underside of the thorax, abdomen, and
legs white; primaries and secondaries white; the costal
margin and apex of the primaries reddish brown.
Expanse 12 inch.
Hab, 5.K. Peru, Santo Domingo, 6000 feet (Mus. Druce).
Hleterocampa lutetlinea, sp. n.
Male.—Ilead, collar, tegule, and thorax dark brown; the
abdomen brown, the base clothed with greenish-yellow hairs,
the underside of the abdomen yellowish white; the legs dark
brown. Primaries dark purplish brown, the costal margin,
apex, outer and inner margin edged with greenish yellow; a
pale greyish double line crosses the wing from the costal to
the inner margin near the base; a large elongated black spot
at the end of the cell and three black spots close to the apex ;
two small white dots just above the anal angle: secondaries
creamy white, the veins dark brown; a large black spot at
the anal angle; the fringe greenish yellow. Underside:
primaries brownish black, whitish on the outer margin near
the anal angle ; secondaries creamy white, the costal margin
brownish black.
Expanse 1? inch.
Hab. §.K. Peru, Santo Domingo, 6000 feet (Jlus. Druce).
Maschane Leecht, sp. n.
Female.—Head, antennex, collar, and teoule reddish fawn-
? ? y) ;)
250 Mr. O. Thomas on new
colour ; thorax, abdomen, and legs pale fawn-colour. Pri-
maries and secondaries pale reddish fawn-colour; primaries
crossed from the apex to the inner margin close to the base by
a dark brown line, lightest on the outer edge. Underside
the same as above, but without any line on the primaries.
Eixpanse 1} inch.
Hab. Amazons (Leech, Mus. Druce).
Maschane neobule, sp. n.
Male.—Head, antenne, and collar yellowish brown ; tegule,
thorax, and abdomen greyish. Primaries yellowish fawn-
colour, almost yellow along the costal margin; a very fine
brown line crosses the wing close to the base; a brown line
extends from the apex to the middle of the inner margin ;
two round dots in the cell and a submarginal row of very
minute brown dots extends from the apex to the anal angle ;
the fringe brown: secondaries reddish brown, palest at the
base. Underside of both wings reddish cream-colour.
Expanse 1? inch.
fab. Costa Rica (Mus. Druce).
XXIX.—New Formsof Saimiri, Saccopteryx, Balantiopteryx,
and Thrichomys from the Neotropical Region. By
OLDFIELD THOMAS.
Saimirt Oerstedi citrinellus, subsp. n.
The Costa Rica form of the Panama S&S. Oerstedi—the
head less blackened, and the limbs less yellow.
General characters as in true Oersted?. Back of the same
vivid orange or orange-ochraceous, or slightly paler, but ante-
riorly that colour narrows between the shoulders, leaving the
region of the shoulder-blades greyish, like the arms. Below,
the belly is scarcely, instead of being strongly, more yellowish
than the white throat and axille, and the groins and inner
sides of the thighs are whitish instead of yellow. Crown of
head either altogether grey, as in S. scdurus, or with the tips
of the hairs blackish, as in S. boliviensis, not deeply black as in
S. Oerstedt. Arms to wrists and legs from thighs downwards
grizzled greyish, with but little yellowish suffusion, these
parts being in Oerstedi strongly suffused with orange-yellow.
Hands orange, of rather a paler shade than in Oerstedz, the
orange running up the outer side of the forearms to the
Forms of Saimiri, Saccopteryx, de. 251
elbow. Feet edged on each side with orange, and the toes
are also the same colour, but the middle line of the meta-
tarsus is grizzled greyish, continuous with the greyish of
the legs. Proximal part of tail grizzled grey like the limbs,
less yellowish than in Oersted’; end of tail black as usual.
Dimensions of the type (measured in skin) :—
Head and body 350 mm.; tail 415 ; hind foot 90.
Skull: greatest length 65; breadth of brain-case 36.
Hab. Costa Rica. Type from Pozo Azul, Pirris.
Type. Adult male. B.M. no. 4.2.7.2. Collected 31 May,
1902, by Mr. C. F. Underwood. Six specimens.
The Squirrel-Monkey of Costa Rica has long been known,
and this very locality, Pirris, is mentioned in Dr. von
Frantzius’s account * of the distribution of what he called
““ Chrysothrix sciurea,”’ identified by Alston with S. Versted/.
But a comparison of the series sent by Mr. Underwood with
those representing the true Oerstedi{, collected in Panama
and Veragua by Messrs. Watson, Batty, and Arcé, shows
that the northern form differs constantly from the southern
in certain characters. Of these the most tangible are the
lessened black of the head, the greyer and less orange suffused
limbs (especially the thighs), and the restriction of the orange
of the feet to their edges, the whole of their upper surfaces
being uniform “ orange-ochraceous ” in the true 8. Oerstedi.
Saccopteryx bilineata centralis, subsp. n.
Similar in all essential respects to the true S. bilineata of
northern South America, but the size is rather less and the
build more delicate, as indicated by the skull. Colour as in
bilineata, but the dorsal lines usually more brownish white, so
that they do not contrast so conspicuously with the general
body-colouar.
Skull, as compared with that of true bilineata, smaller
(total length 15°5 mm. as against 17) and more lightly built.
Crests and ridges less developed, postorbital processes smaller
and weaker. Brain-case more inflated at its antero-external-
superior corners, the convexity markedly stronger and more
projecting than in the larger form. ‘Teeth smaller throughout.
Dimensions of the type (measured in spirit) :—
Forearm 47 mm.
* Arch. f. Nat. xxxv. p. 260 (1869).
t The type locality of S. Oersted2 is not, as stated by Miller and Rehn,
Cartago, Costa Rica, but Chiriqui, whence Oersted’s specimen had been
brought alive to Cartago. The original figure and description agree
with Chiriqui specimens in all the characters distinguishing the latter
from the Costa Rican form.
252 Mr. O. Thomas on new
Head and body 50; tail 14; lower leg and foot (s. u.) 80°5 ;
calear 18:5.
Skull: greatest length 15:6; basal length in middle line
12; greatest breadth 10°4; interorbital breadth 4:2 ; breadth
of brain-case 8; palate length 5:4; front of upper canine to
back of m?’ 6:5; front of lower canine to back of mg 6°8.
Hab. (of type). Teapa, Tabasco, S.E. Mexico. Other
specimens from Guatemala and Costa Rica.
Type. Female. B.M. no. 88. 8. 8. 20. Collected by
H. H. Smith, and presented by Messrs. O. Salvin and F. D.
Godman. About a dozen specimens examined.
The large members (forearms 45-50 mm.) of the restricted
genus Saccopterye are remarkably uniform in character over
a wide geographical area, series from Heuador and Peru on
the west to Pernambuco on the east and Trinidad and Guiana
in the north presenting no differences not covered by indi-
vidual variation at single localities. J am therefore quite
unable to distinguish Mr, Miller’s S. perspicillifer (forearm
45-50) of Trinidad from the original S. dilineata (forearm
45 mm.) of Surinam. The large skull with heavy postorbital
processes, as described by Miller, is equally to be found in
specimens from Guiana, Para, and Pernambuco, which must
among them include the true dc//neata of Surinam. Examples
with the typical length of forearm (45 mm.) occur both
among our ‘Trinidad and Guianan series, without any cranial
indication that they belong to a different form from those
whose forearms attain to 48 or 50 mm.
In Central America, however, the representative of S. d7-
lineata seems sufficiently modified to bear a subspecific
name, being distinguished by its lighter skull, more cube-
shaped brain-case, smaller teeth, and rather duller coloration,
But even then the difference is but slight.
The still smaller species of this group are two in number—
S. leptura, Schr., browner in colour, with a skull of about
13°5-14 mm. ,and a forearm averaging about 38-40 mm. ; and
SS. canescens, Thos., grey, skull only 12°5-13 mm., and length
of forearm about 36-38 mm. Of the last-named, besides the
type from the Lower Amazon, the Museum contains examples
from the Orinoco (Cherrie), Surinam (Bartlett), and Cayenne
( Cherrie), in each of which places S. leptura also occurs.
Balantiopteryx io, sp. n.
A slenderly built species allied to B. infusca *.
Size very small, the trunk and forearm lengths markedly
* Saccopteryx infusca, Thos. Aun. & Mag. Nat. Hist. (6) xx. p, 546
(1807).
Forms of Saimiri, Saccopteryx, &c. 253
less than in B, tnfusca, though the skull is as large as in that
animal. General characters very much as in B. infusca ;
ears as in that species, the inner margin more evidently
concave just below the tip. Tragus slender, its tip rounded,
a marked lobule opposite to base of its inner margin, and
another slight projection higher up. Wing- and leg-bones
remarkably slender, much more so than in B. cnfusca. Wing-
sacs in the centre of the membrane, as usual in Ba/lantio-
pteryx, about a quarter of an inch internal to a line drawn
directly forwards from the elbow. Feet quite free of mem-
brane, the wings attached to the distal end of the tibie.
Calcars slender, not reaching upwards to the knee. Base of
interfemoral membrane hairy as far as the exsertion of the
tail.
Colour of body above and below, and of membranes, dark
brown (in alcohol) ; no white line along hinder edge of wings.
Skull agreeing in size with that of B. c¢nfusca, therefore
much larger in proportion to the size of the animal than in
that species. Muzzle flatter than in that species, and the
inflations smaller, though equally prominent ; in B. tnfusca
the two inflations meet in the middle line for about 2 mm.,
while in B. to they are quite separate from one another, the
nasal region having a marked concavity between them,
bordered in front by an upturned edge above the centre of
the nostrils. Zygomata abruptly and widely expanded.
Front edge of palate with a well-marked median spine.
Posterior narial fossa widely open, its outline broadly
U-shaped. Basisphenoid pit large, more extended longi-
tudinally than in B. ¢nfusca, longer than broad, without trace
of median septum. ‘l'eeth apparently as in the allied species.
Dimensions of the type (measured in spirit) :—
Forearm 36 mm.
Head and body 40; tail 12; tail free of membrane 4 ;
ear 12; tragus on inner edge 3; thumb 5:6; third finger,
metacarpal 31°5, first phalanx 11, second phalanx 15; fifth
finger 36; tibia 14 ; lower leg and foot (c.u.) 22; calcar 10°5.
Skull: greatest length 12°3; upper length in middle line
11°4; basal length in middle line 8:7; zygomatic breadth
8°83; breadth across muzzle 6; mastoid breadth 7°6;. palate
length 3:3 ; basisphenoid pit 3:1 x 2°7.
Hab. R. Dolores, near Coban, Guatemala.
Type. Adult male. B.M. no. 86. 9.3.1. Collected by
Mr. F.C. Sarg. ‘Two specimens.
These are the Guatemalan specimens referred by me to
B. infusca when describing that species, but there can be no
doubt as to their distinctness both in proportions and skull-
characters.
254 On new Forms of Saimiri, Saccopteryx, ce.
Thrichomys laurentius, sp. n.
Closely allied to 7. apereoides, but greyer and with less
tufted tail.
Fur close and straight, rather shorter than in 7. apereotdes;
hairs of back about 18-20 mm. in length. General colour
above approximately “ broccoli-brown,” the individual hairs
slaty grey below, paler at base, darkening outwards, with a buffy
subterminal band and a black tip. Sides, especially shoulders
and hips, paler and greyer. Under surface, except for a
greyish collar, pure sharply defined white, the hairs white to
their bases. Head dark grey, a whitish spot above eye,
another below it, and a third at outer base of ear. Long
hairs of ear black. Arms and legs greyish, like sides ex-
ternally, white on their inner aspects ; hands and feet mixed
grey and white along the metapodials, pure white laterally and
on the digits. Tail with about an inch at its base clothed
with hair of the texture and colour of that on the rump; the
remainder cylindrical, well-haired, but not markedly crested
above, and the hairs scarcely increasing in length terminally,
the longest hairs barely attaining 8mm. In 7’ apereoides the
upper surface is crested with hairs which increase in length
to the end, where they attain 15-18 mm. Colour of tail
black above and at the end, dull whitish proximally below.
Skull on the whole as in 7. apereoides, but the nasals are
longer and the palatal foramina are more widely open, in
this respect approaching those of 7. Fosteri. Last molars
similar to those of 7. apereotdes, less complicated than is
usually the case in 7. Postert.
Dimensions of the type (measured in the flesh) :—
Head and body 215 mm.; tail 195 ; hind foot (s. u.) 45 ;
ear 21.
Skull: greatest length 56°7 ; basilar length 41 ; greatest
breadth 26; nasals 20°5x6°5; interorbital breadth 11:3;
breadth across postorbital projections 17°2; palate length
19:8; diastema 11; palatal foramina 5°8 x 4-4; length of
upper molar series 8°6.
Hab. Sio Lourengo, near Pernambuco, Alt. 50 m.
Type. Old male. B.M. no. 3. 10. 1.68. Original number
1721. Collected 16 August, 1903, by Alphonse Robert.
By the discovery of the present animal the range of the
genus Thrichomys is very considerably extended. Till
recently only recorded from Lagoa Santa (Lund and Rein-
hardt), it was found in Paraguay by Mr. W. Foster, who
has now sent a considerable series of the local species to
the British Museum. In that country it is found only “in
On Fishes from Mexico and British ITonduras. 255
a small area of tumbled rock, a few acres in extent,” and
Mr. Robert informs me that 7. /aurentius is similarly very
lceal in its distribution. He never met with it in any of the
other places where he has collected.
Thrichomys laurentius has four mamme, one pair placed
high up on the flank behind the axilla, and a second pair
4-5 cm. further back in front of the hips. No doubt the
other species are similar in this respect.
T. laurentius is most nearly allied to T. apereoides, but may
be distinguished by its darker colour and less bushy and
crested tail. J. Posteri, with a tail like that of 7. apereotdes,
has a rather more greyish belly, wider palatal foramina, and
more complicated third molars.
XX X.—Descriptions of new or little-known Fishes from
Mexico and British Honduras. By C. Tare ReGan, B.A.
Clupea (Opisthonema) Bulleri, sp. n.
Depth of body 33-32 times in the total length, length of
head 4 times. Snout as long as or a little longer than eye,
the diameter of which is 4 times in the length of head.
Maxillary extending to below anterior } of eye; lower jaw
projecting. Sc. 48-50/16. D.17. A. 20-21. Last dorsal
ray elongate. Origin of dorsal in advance of ventral, a
little behind the vertical from the tip of pectoral. Pectoral
& the length of head, extending back a little more than 2 the
distance from its base to the anal. Silvery below, darker
above; amore or less distinct dark spot on the shoulder ;
dorsal and caudal dusky.
Total length 127 mm.
Two specimens from Las Pefias, Jalisco, Mexico, collected
by Dr. Buller.
This species is closely allied to C. thrissa, Brouss., but is
distinguished by the smaller eye, lower jaw somewhat pro-
jecting, and no rows of dark spots on the upper part of the
body.
Engraulis (Stolephorus) argentivittatus, sp. n.
Depth ot body about 6 times in the total length, length of
head 33 times. Snout nearly as long as eye, the diameter of
which is 43-43 times in the length of head. Maxillary ex-
tending about to posterior edge of preoperculum, D, 12-13,
256 Mr. C. 'T. Regan on new or little-known
its origin midway between nostril and base of caudal.
A. 16-17, commencing a little behind the end of dorsal.
Pectoral less than 4 the length of head. Scales deciduous.
A well-defined silvery lateral band as broad as the eye.
Total length 75 mm.
Three specimens from Las Pefias, Jalisco, Mexico, collected
by Dr. Buller.
Allied to £. perfasciatus, Poey, but with longer head,
smaller eye, and shorter pectoral.
Pseudoxiphophorus pauciradiatus, sp. n.
Xiphophorus bimaculatus (part.), Heck. Sitzb. Ak. Wien, 1848, p. 297,
pl. ix. fig. 2.
Pseudoxiphophorus bimaculatus (part.), Woolm. Bull. U.S. Fish.Comm.,
xiv. 1894, p. 65; Jord. & Kyerm, Fish. N. Am. p. 678 (1896).
Depth of body 33-4 times in the total length, length of
head 33-41 times. Snout not longer than eye, the diameter
of which is 33-4 times in the length of head, and 2-24 times
in the interorbital width. 29-30 scales in a longitudinal
series. D, 11-13, its origin nearer to base of caudal than to
tip of snout, the length of its base about 4 times in the total
length. A. 9-10, commencing in advance of the dorsal in
the male, and slightly behind the dorsal in the female.
Pectoral 3-3? the length of head. Brownish, each scale with
a darker intramarginal crescent; a black spot on the shoulder
and another on the upper part of the base of caudal; dorsal
with 2 series of small blackish spots.
Total length 76 mm.
Eight specimens from Orizaba, Mexico, collected by Mr. A.
J. Woolman.
Two species have been confounded under the name of
P. bimaculatus, and it seems probable that the specimens
described and figured by Heller as females belong to the one
described above. P. bimaculatus (of which P. reticulatus,
Trosch., is a synonym) must be restricted to the species of
which Heckel described and figured a male specimen and
which has been redescribed by Steindachner. It differs
from P. pauctradiatus in having a longer head and longer
snout, and in the dorsal fin with 14-16 rays commencing
midway between tip of snout and base of caudal, its base about
+ of the total length.
Zoogoneticus maculatus, sp. n.
Depth of body 34-32 times in the total length, length of
head 3 times. Snout as long as eye, the diameter of which
Fishes from Mexico and British Honduras. 207
is 4-44 times in the length of head, interorbital width 24-23
times. Mouth moderate, oblique, the lower jaw prominent.
Se. 36-38. D. 13-14, its origin about equidistant from
posterior edge of preoperculum and base of caudal, its longest
ray (the fourth or fifth) a little longer than the base of the
fin, which is 3} the length of head or less. A. 15, commencing
a little behind the dorsal, the first six rays, in the male, short,
stiff, and of equal length. Pectoral 3-2 the length of head,
Ventrals extending to the vent. Caudal truncate. Caudal
peduncle 12-2 times as long as deep. Brownish above,
silvery below, with dark spots which are most conspicuous
posteriorly ; fins immaculate.
Total length 84 mm.
Three specimens from the Rio Santiago, Mexico, collected
by Dr. A. C. Buller.
Z. pachycephalus, Gthr., and the very closely allied
Z. quitzeoensis and Z. robustus of Bean, agree with this species
in the number of dorsal and anal rays, but have a shorter
and broader head and the caudal peduncle about as long
as deep.
Dr. Meek includes Fundulus guatemalensis, Gthr., and
f, labialis, Gthr., in Zoogoneticus, but in neither of them is
there any differentiation of the anterior anal rays in the male.
In the former the anal fin is similar in both sexes, in the
latter it is larger in the female, and from the specimens in
the British Museum one would judge that these species are
not viviparous.
Characodon Geddesi, sp. n.
Depth of body 23-3 (males) or about 24 (pregnant females)
times in the total length, length of head 32-4 times. Snout
as long as eye, the diameter of which is 4-4} times in the
length of head, interorbital width about 24 times. About
17 rather short gill-rakers on anterior arch. Sc. 39-42.
D. 18-20, its origin nearly equidistant from posterior margin
of operculum and base of caudal. A. 21-23, commencing a
little behind the dorsal, not modified in the male. Pectoral
nearly 3 length of head. Ventrals extending to the vent.
Caudal truncate. Caudal peduncle 13-1? times as long as
deep. Olivaceous, silvery below, with several darker narrow
vertical bands on the upper half of the body.
Total length 70 mm.
Numerous examples of this viviparous species from Lake
Tezcoco, Southern Mexico, collected by Mr. P. Geddes.
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 17
258 On Fishes from Mexico and British Honduras.
Heros (Cichlasoma) octofasciatus.
mes acta OU Hs, Regan, Revue Suisse Zool. xi. 1903, p. 417, pl. xiii.
el.
Depth of body 2-22 times in the total length, length of
head 23-3 times. Snout nearly as long as or a little longer
than the eye, the diameter of which is 3}—4} times in the
length of head, interorbital width about 3 times. Maxillary
extending to vertical from anterior margin of eye; breadth
of preorbital }-# diameter of eye; cheek with 5 or 6 series
of scales; fold of lower lip interrnpted in the middle. Sc.
28-3] =, 31-4 scales between the upper lateral line and
the scaly sheath at the base of the soft dorsal. D. XVII-
XIX 8-10. <A. VITI-X 7-8. Dorsal commencing above
or a little before the axil of pectoral, the spines increasing in
length to the sixth or seventh, which is 23-34 times in the
length of head, thence subequal ; soft dorsal and anal pointed;
pectoral 3-4 length of head; ventrals extending to the base
of fourth or fifth anal spine; caudal rounded; caudal peduncle
1$-21 times aslong as deep. In the young dark cross-bands
on the body, which become indistinct in the adult; a dark
blotch on the middle of the side below the lateral line and
another on the upper half of the base of the caudal, this latter
often ocellated; in the adult a dark band running from the
eye to the blotch on the side; usually some light blue spots
on the head and one on each scale of the side of the body ;
vertical fins with small dark spots.
Total length 130 mm.
Several examples from British Honduras, collected by the
Rev. J. Robertson.
I am glad to be able to give a more complete account of
this species, which was originally described from a little
example of 50 mm. It is closely allied to H. multispinosus,
Gthr., which has much stronger and longer dorsal spines,
and to H. nigrofasciatus, Gthr., which has a broader pre-
orbital and only 24 scales between the upper lateral line and
the sheath at the base of the soft dorsal fin.
Heros (Heros) callolepis, sp. n.
Depth of body about 2 times in the total length, length
of head 3 times. Eye nearer to posterior edge of operculum
than to end of snout, its diameter 34 times in the length of
head and equal to the interorbital width. Maxillary not
extending to below the eye; breadth of preorbital equal to
the diameter of eye; cheek with 4 or 5 series of scales; lower
On Holocentrum osculum, Poey. 259
lip witha strong continuous fold. Sc. 28-29%, 11-2 between
upper lateral line and base of soft dorsal. LL. lat. 18-20 +10.
D. XV 9-10. A. VI-VII 7-8. Dorsal commencing behind
axil of pectoral, the spines rather weak, the last 21-23 times
in the Jength of head and not longer than the last of the
anal ; soft dorsal and anal pointed; pectoral about 2 the
length of head; ventral extending beyond origin of anal;
caudal weakly emarginate ; caudal peduncle as long as deep.
Brownish, with small light blue spots on the head and one
at the base of each scale on the body; a dark blotch on the
lateral line below the 13th-15th dorsal spines.
Total length 100 mm.
Two specimens from Santo Domingo de Guzman, Mexico,
collected by Dr. A. C. Buller.
Heros aureus, Gthr., is distinguished by the deeper body
(depth 2-24 in the total length), smaller scales (33 =), and
longer dorsal spines (the last 4 the length of head).
XX XI.— Descriptions of Holocentrum osculum, Poey, and of
a new Fish of the Genus Centropomus. By C. Tate
REGAN, B.A.
AmonGst the fishes collected by Dr. R. Bowdler Sharpe in
the West Indies are several examples of a Holocentrum which
I have no doubt is the little-known H, osculum of Poey, and
as such I describe it below. I also take the opportunity to
describe a new Centropomus from the West Indies.
Holocentrum osculum.
Holocentrum osculum, Poey, Memorias, ii. p. 156 (1860),
Holocentrum perlatum, Poey, t.c. p. 157.
Depth of body 3-32 times in the total length (without
caudal) and nearly equal to the length of head (opercular
spine included). Snout equal in length to the interorbital
width, 3-3 the diameter of eye, which is 3 times in the length
of head. Maxillary extending to below anterior edge of
pupil, the width of its distal extremity 2 the diameter of
eye. Opercular spine strong, with 1 or 2 more or less dis-
tinct much shorter spines below; preopercular spine extending
back far beyond the subopercular margin; preorbital strongly
serrated and with an anterior downwardly directed spine.
15-16 gill-rakers on the lower part of anno arch,
Lg
260 On a new Fish of the Genus Centropomus.
Sc. 58-57, 2. D. XI, 1 14-15, the fourth, fifth and sixth
spines the longest, about 4 the length of head, the soft fin
elevated and pointed, extending beyond the base of caudal
when laid back. A. IV 10-11, the third spine the strongest
and longest, 3-2 the length of head, Pectoral about 2 the
length of head. Upper lobe of caudal the longest. Caudal
peduncle 22-3 times as long as deep. Purplish, with bronze
longitudinal stripes between the series of scales; fins pale.
Total length 210 mm.
Eight examples from St. Thomas and St. Croix; (thespecies
originally recorded from Cuba).
This species is closely allied to H. sogo, Bl. (i. longi-
pinne, C. & V.), from which it differs notably in the smaller
mouth, more slender caudal peduncle, and the shape of the
spinous dorsal fin.
Centropomus argenteus, sp. n.
Centropomus parallelus (part.), Bouleng, Cat. Fish. i. p. 869 (1895).
Depth of body 33-4 times in the total length, length of
head (excluding the subopercular flap) 22 times. Snout
much longer than the eye, the diameter of which is about
42 times in the length of head, and equal to its distance from
the posterior edge of preeoperculum. Maxillary extending to
below middle of eye ; lower jaw strongly projecting. Sub-
opercular flap extending to below origin of dorsal. Cheeks
and opercles scaly. Praorbital and supraclavicle serrated ;
preoperculum serrated, with stronger spines at the angle,
anterior ridge with two spines. 7-9 gill-rakers and 4-6
rudiments on lower part of anterior arch. 67-70 scales in a
longitudinal series, 8 or 9 in a transverse series from origin
of second dorsal to lateral line. D. VIII, I 10, originating
behind the axil of pectoral, the third and fourth spines the
longest, about $ the length of head. A. III, 6, second anal
spine stronger anda little longer than the third, as long as
or a little longer than the caudal peduncle, 3-3 the length of
head. Pectoral # the length of head. Ventrals inserted
well behind pectorals, extending back a little beyond the
vent, which is situated at 3 the distance from base of ventral
spine to origin of anal. Silvery, back darker; lateral line
not blackish; spinous dorsal slightly dusky, fins otherwise
yale.
Total length 135 mm.
Three specimens, two from Barbadoes (presented by
Mr. F. G. Beckford in 1872) and one from British Guiana.
C. parallelus is easily distinguished by the shorter snout,
On Two new Frogs from Cameroon. 261
larger eye (diameter 4 times in length of head, equal to length
of snout, and considerably greater than the distance from
posterior edge of preoperculum in specimens of this size), the
smaller scales (75-90 ““*), and the much more anterior vent.
C. argenteus is quite as closely allied to C. ensiferus, Poey,
which has larger scales (50-60) and a longer pectoral, and
also differs in many other characters. There can be no
doubt as to the identity of C. mextcanus, Bocourt, with
C. parallelus. The British Museum possesses several ex-
amples from Mexico, in some of which the lateral line is
more or less pigmented. C. constantinus, Jord. & Everm.,
appears to me to be at least very closely allied to C. un-
decimalis, Bl., a species with which they do not compare it.
XXXII.—Descriptions of Two new Genera of Frogs of the
Family Ranidee from Cameroon. By G. A. BOULENGER,
Bh.
NYCTIBATES.
Pupil vertical. Tongue cordiform, free and notched
behind. Vomerine teeth. Tympanum distinct. Fingers
free, toes webbed. Outer metatarsals bound together. Omo-
sternum and sternum cartilaginous. Terminal phalanges
simple, obtuse.
Closely related to T'richobatrachus, Bler.
Nyctibates corrugatus.
Vomerine teeth in two small rounded groups between the
large choane. Head large, as long as broad ; snout as long
as the orbit, obliquely truncate and slanting forwards from
the nostrils to the mouth; canthus rostralis strong; loreal
region concave; nostril equally distant from the eye and
from the end of the snout; eye large; interorbital space as
broad as the upper eyelid ; tympanum three fifths the diameter
of the eye. Limbs rather slender; tips of fingers and toes
slightly swollen ; first finger a little longer than second; toes
half-webbed ; subarticular tubercles strong; a small, oval,
inner metatarsal tubercle. The tibio-tarsal articulation reaches
the eye. Upper parts with small granular asperities ; back
with fine oblique folds converging posteriorly, forming more
262 On Two new Frogs from Cameroon.
or less regular chevrons; lower parts smooth. Purplish
brown above ; a triangular dark marking with a fine light
edge between the eyes, the base turned forwards; upper lip
white-edged; limbs with narrow, oblique, dark cross-bars ;
sides of thigh and inner side of leg blackish, speckled with
whitish ; lower parts whitish, with the exception of a con-
siderable part of the thigh, the tarsus, and the foot, which
are blackish brown.
From snout to vent 53 mm.
Two female specimens were obtained at Efulen, Bulu
Country, Southern Cameroon, by Mr. G. L. Bates.
BuLvA.
Pupil horizontal. Tongue cordiform, free and notched
behind. Vomerine teeth forming long transverse series
behind the choane. ‘Tympanum distinct. Fingers and toes
free. Outer metatarsals bound together. Omosternum and
sternum cartilaginous. Terminal phalanges simple, obtuse.
A very distinct genus, to be placed near Petropedetes,
Reichen.
Bulua ventrimarmorata.
Vomerine teeth in two curved series narrowly separated
from each other and extending outwards beyond the choane.
Head moderate, rather strongly depressed, a little broader
than long; snout short, broadly rounded; no canthus ros-
tralis; eye small; interorbital region twice as broad as the
upper eyelid ; tympanum a little smaller than the eye, its
diameter equal to its distance from the orbit. Fingers rather
short, blunt, first much longer than second ; toes moderate,
with swollen tips ; subarticular and inner metatarsal tubercles
feebly prominent. The tibio-tarsal articulation reaches the
tympanum. Skin smooth. Dark purplish brown above,
with indistinct darker markings ; a pink spot on each side
of the vent; sides of head and of thighs black, speckled
with white ; limbs with interrupted dark cross-bars; throat
black ; belly and lower surface of limbs marbled black and
white. Breeding male with two groups of rather large,
conical, black, horny spines on the inner side of the inner
finger.
From snout to vent 40 mm.
A single male specimen from Efulen, Bulu Country,
collected by Mr. G. L. Bates.
On Heteroptera from North Queensland. 263
XXXII.—Lhynchotal Notes—XXII. By W.L. Disranr.
HETEROPTERA FROM NorTH QUEENSLAND.
Tue British Museum has recently acquired a collection of
Rhynchota made by Mr. F. P. Dodd at Townsville, North
Queensland, Although this order of insects is at present
very imperfectly known from the continent of Australia,
a sufficient number of genera and species have been described
to establish by their comparison that, so far as the Rhynchota
are concerned, Northern Queensland represents or belongs to
a separate province in the zoo-geographical divisions of
Australia. The Heteroptera are alone dealt with in this
paper, the Homoptera being reserved for some future occasion.
The types are all in the National Collection.
Fam. Pentatomide.
Theseus nigrescens, sp. 0.
Ochraceous or stramineous, blackly punctate, the punctures
arranged in longitudinal series on head and on anterior area
of pronotum, those at lateral margins being continuous ;
antenne, sometimes a large spot on basal area of pronotum,
scutellum, membrane, body beneath, and legs black ; basal
half of fourth, extreme base of fifth, and inner margin of first
joint of antenne, basal lateral margins, apex, and sometimes
a small basal spot to scutellum, coxe, trochanters, longi-
tudinal streaks to femora, a broad subbasal annulation to
tibie, tarsi (excluding apices), lateral margins of body
beneath, and discal spots to abdomen pale ochraceous.
Allied to T. modestus, Stal ; scutellum black, more thickly,
less confluently, and more finely punctate, and with a very
distinct central longitudinal ridge on its posterior area,
Long. 123 mm.
Eumecopus abdominalis, sp. n.
Above reddish brown, irrorated with ochraceous, much
more strongly so on corium; head with the lateral margins,
a central longitudinal fascia, margined on each side by a
shorter fascia on anterior area, and a slender curved line on
posterior area, narrow lateral and posterior margins, a central
linear spot at anterior margin, and two small discal spots on
anterior area of pronotum, a large spot at each basal angle
and the apex of scutellum, and marginal and venal lines to
264 Mr. W. L. Distant on
corium very pale ochraceous or stramineous ; membrane
black ; connexivum above and beneath flavous; abdomen
beneath and apex of rostrum castaneous; sternum, legs,
antenne, and a spot on apical abdominal segment reddish
ochraceous; outer streaks to femora, basal areas of tibize, and
the tarsi flavescent; apical segmental abdominal angles
flavescent ; rostrum reaching, but not passing, the third
abdominal segment; antenne five-jointed, second joint
scarcely more than half the length of third ; lateral posterior
angles of pronotum spinously produced, spines distinctly
recurved.
Long. 18; exp. pronot. angl. 95 mm.
Eumecopus pallescens, sp. n.
Above pale stramineous, thickly piceously punctate, the
punctures more confluent at lateral areas of pronotum and
scutellum and in a central longitudinal streak to corium ;
head with the punctures in longitudinal series, the ocelli
bright carmine-red; lateral margins of pronotum, scutellum
and corium, a central longitudinal fascia to pronotum and
scutellum, and apex of the last pale stramineous, impunctate ;
connexivum flavescent, inwardly darkly punctate; membrane
piceous, its apical area paler ; body beneath and legs pale
ochraceous; apex of rostrum and stigmatal spots black ;
linear streaks to femora and tibia, apices of posterior femora
and tibie, and apices of the tarsi brownish castaneous ;
antenne pale brownish, bases of the second, third, and fourth
joints a little paler in hue; apical segmental abdominal
angles flavescent ; rostrum reaching the fourth abdominal
segment; antennee four-jointed, second and third joints
longest, second a little longer than third; lateral posterior
angles of pronotum spinously straightly produced.
Long. 19-20; exp. pronot. ang]. 8-85 mm.
DANDINUS, gen. nov.
Elongately ovate ; head broad and elongate, almost as
long as the pronotum, its lateral margins a little sinuate, its
apex slightly widened and rounded, lateral lobes a little
longer than the central lobe, their apices inwardly angulated
but not meeting ; eyes small, touching the anterior margin
of the pronotum; antennze five-jointed, almost as long as
head and pronotum together, first joint almost hidden
beneath head, a little incrassate, second and third more
slender, second longer than third, fourth and fifth thickened,
Heteroptera from North Queensland. 269
subpyriform, about subequal in length; rostrum reaching
posterior coxze (imperfectly seen on carded specimen) ; pro-
notum about twice as broad between posterior lateral angles
as at anterior margin, anterior lateral angles obtusely acute,
very strongly transversely impressed near middle, the anterior
area possessing a broad central carination with a tuberculous
eallosity on each side, the whole surface rugosely punctate ;
scutellum long, broad, passing apex of corium, very broad at
base, obliquely narrowed to about middle, the lateral margins
then parallel to apex, which is broadly rounded, basal area
rugosely gibbous; corium moderately small and narrow, not
reaching apex of scutellum; membrane short, with coarse
reticulate venation; connexivum broadly exposed beyond
middle ; legs short, femora a little thickened.
Dandinus may be placed near the Ethiopian genus
Aischrus, Spin.
Dandinus crassus, sp. 1.
Irregularly greyish brown, thickly coarsely punctate ; first,
second, and third joints of antenne, central discal fascia and
some oblique discal lines on posterior area of pronotum,
connexivum, and legs ochraceous ; fourth and fifth joints of
antenne, annulations to femora and tibie, and basal area of
scutellum piceous ; an oblique linear stramineous spot at each,
basal angle of scutellum, its subapical area and inner area of
corium greyish punctured with piceous ; connexivum spotted
with piceous ; body beneath piceous, the lateral areas more
or less brownish ochraceous ; head somewhat obscurely pune-
tate; pronotum thickly, coarsely, rugosely punctate ; scutellum
thickly, coarsely, rugosely punctate on basal area, coarsely and
more sparingly punctate on posterior area, which has a distinct
central carination extending for about half its length; corium
sparingly and a little more finely punctate; connexivum
inwardly coarsely punctate.
Long. 53; exp. pronot. angl. 34 mm.
Fam. Coreide.
Subfam. Corzryz.
POMPONATIUS, gen. nov.
Body elongate, narrowed posteriorly ; head broad, not
produced beyond the antenniferous tubercles, a deep central
longitudinal incision on disk, and a distinct transverse conical
ridge at base; eyes longer than broad, compressed at lateral
266 Mr. W. L. Distant on
margins of head ; antenne with the first, second, and third
joints subequal in length, fourth shortest, first and second
regularly moderately incrassate, third and fourth pyriform ;
rostrum reaching the middle of mesonotum; pronotum about
as long as broad at base, anterior margin concavely sinuate,
the anterior angles acute, lateral margins carinate, slightly
upwardly reflected, posterior lateral angles nodulose, base
obliquely deflected, truncate in front of scutellum and then
obliquely directed to the lateral angles; scutellum small,
triangular ; corium long, reaching the base of the sixth
abdominal segment; membrane very small, with reticulate
venation; lateral margins of abdomen beyond middle am-
pliately produced and moderately directed upward, the
posterior apical angles of the fifth and sixth segments acute,
the apex of the anal appendage in ¢ angularly bifurcate ;
legs short, femora apically incrassate, with a distinct tooth
beneath near apex, posterior femora only extending to about
half the length of abdomen ; abdominal spiracles at about
equal distance from anterior and lateral segmental margins.
Allied to Cherommatus.
Pomponatius typicus, sp. n.
9. Testaceous, base of pronotum and corium with piceous
and flavous suffusions ; head with two central fuscous fasciz ;
scutellum with a black central line at base; membrane
bronzy black ; body beneath reddish ochraceous, two black
fasciee extending from anterior to posterior coxe, and two
black spots on basal abdominal segment behind inner margins
of coxe, on mesonotum the fascize have a broad outer greyish
margin, outwardly speckled with black; legs stramineous,
finely speckled with black, a little darker at bases and apices
of tibiz ; above finely and obscurely punctate, beneath a little
more distinctly punctate ; membrane not quite reaching apex
of abdomen.
Long. 153 mm.
Fam. Lygeide.
Subfam. Gzocorivz.
Germalus lineolosus, sp. n.
Ochraceous, with dark punctures, fuscous or piceous lines,
and piceous suffusions to hemelytra. Head pale ochraceous,
impunctate, a central longitudinal line and a shorter line at
each ocellus piceous ; antenne ochraceous, apices of apical
joints, and eyes reddish; pronotum pale ochraceous, darkly
Lletercptera from North Queensland. 267
punctate, except on anterior transverse callosities and basal
margin, the first of which have a central piceous spot and the
second has six spots of the same colour, the disk with four
fuscous lines, two central and one on each lateral area; scu-
tellum ochraceous, with two central piceous spots, a transverse
line of dark punctures near base, and the apical area darkly
punctate; corium pale ochraceous, subhyaline, the claval
suture and longitudinal veins punctate, apical area more or
less suffused with piceous; membrane pale fuscous hyaline ;
connexivum ochraceous, spotted with rosy red; body beneath
and legs ochraceous; lateral areas of sternum thickly darkly
punctate ; abdomen with a submarginal rosy-red, sometimes
piceous, fascia.
Long. 43-5 mm.
Geocoris elegantulus, sp. n.
Head, pronotum, and sternum ochraceous; scutellum,
hemelytra, and abdomen beneath black; anterior and pos-
terior margins of pronotum, clavus, claval suture, lateral
margins of corium, and narrow lateral margins of abdomen
beneath creamy white ; legs pale ochraceous, apices of tarsi
fuscous ; antenne piceous, first joint (excluding apex) and
the whole of the apical joint pale ochraceous, second and
fourth joints subequal in length; eyes carmine-red, directed
backward to about one third the length of pronotum; pro-
notum coarsely punctate behind the anterior and before the
posterior margin ; scutellum finely punctate; clavus and a
submarginal line to corium coarsely punctate; body above
sparingly, finely, longly pilose.
Long. 3 mm.
Subfam. A pxanivz.
Pamera picturatus, sp. n.
Black ; first and second joints of antenna, femora, a sub-
apical annulation to anterior and intermediate tibiz, and
basal margin of pronotum testaceous red; corium ochraceous,
with the subapical area creamy white, a middle marginal
line, an interior marginal line to the white area, and the
apical angle indigo-black; membrane indigo-black, the apex
broadly dull ochraceous ; abdomen beneath with a central
creamy-white transverse fascia; second joint of antennz
much longer than third and subequal to fourth; anterior lobe
of pronotum elongate, globose, slightly shorter than head and
at least half as long again as posterior lobe; corium finely
268 Mr. W. L. Distant on
sparingly punctate ; anterior femora strongly incrassate,
lonely pilose above, finely spinose beneath ; tibia moderately
curved ; body above sparingly longly pilose.
Long. 63 mm.
Allied to P. cephalotes, Dall.
Pamera apicalis, sp. n.
Black ; basal joint of anterior and intermediate tarsi and
a broad apical spot to membrane dull ochraceous; corium
creamy white, thickly darkly punctate, subclaval margin, a
transverse central fascia, and the apical margin black ;
abdomen beneath in female with a central transverse creamy-
white fascia and the apex dull ochraceous; head, pronotum,
and scutellum greyishly pilose, base of pronotum nude; apex
of scutellum pale stramineous; anterior femora strongly
incrassate, finely spinose beneath, longly pilose above, tibize
nearly straight ; other characters as described in preceding
species.
Long. 53-6 mm.
Dieuches scutellatus, sp. n.
Black; lateral margins of anterior lobe of pronotum
creamy white; basal joint of antennzs and extreme bases of
anterior tibize brownish ochraceous; a central linear spot to
posterior lobe of pronotum, two small subbasal spots and
apex to scutellum, base, a central marginal spot, two small
spots near claval margin, and a large subapical spot to
corium creamy white; membrane dark fuliginous, its apex
paler ; bases of intermediate and posterior femora broadly
creamy white ; posterior lobe of pronotum very coarsely
punctate, its posterior margin concavely sinuate, anterior
iste much more finely punctate, its lateral margins very
slightly convex ; second, third, and fourth joints of antenne
almost subequal in length ; anterior femora incrassate, some-
what strongly spinose beneath.
Long. 64-7 mm.
Allied to D. atricornis, Stal.
Dieuches consanguineus, sp. n.
Black; lateral margins of pronotum (excluding base),
bases of first and fourth joints of antenne (broadly), and bases
of second and third joints (narrowly), trochanters, bases of
femora, and the anterior and intermediate tibia (excluding
apices) stramineous ; apex of scutellum and the corium strami-
neous, the last with a broad transverse medial fascia and the
Heteroptera from North Queensland. 269
apical margin black, the inner basal area and clavus much
suffused with brownish black; connexivum stramineous,
spotted with black; second, third, and fourth joints of
antennz subequal in length; lateral margins of pronotum
almost obliquely straight, very slightly sinuate, transversely
impressed near middle and concave at base.
Long. 74-9 mm.
Allied to D. longicollis, Dall.
Fam. Reduviide.
Havinthus trochanterus, sp. n.
Black, shining; apex of scutellum, venation to corium,
and the trochanters sanguineous; corium and clavus sparingly
greyishly tomentose ; connexivum with large marginal
sanguineous spots ; head about as long as pronotum and
scutellum together, its lateral margins behind eyes granulate ;
ocelli castaneous ; antenne: with the first joint as long as
head, second and third short, together about as long as
fourth ; pronotum strongly constricted near middle, anterior
lobe glabrous, posterior lobe very finely and obscurely
punctate; connexivum robust, erosed at the segmental
incisures ; femora finely granulate, anterior femora _pro-
minently spinose beneath, intermediate and posterior femora
more obsoletely spinose.
Long. 114-12 mm.
A distinct species by the greyishly tomentose and san-
guineously veined corium and the sanguineous trochanters,
Fam. Capside.
Subfam. Mrrem2z.
Division MIRARIA.
Megalocerea Doddi, sp. n.
Elongate, slender; pale ochraceous, with a slight virescent
tinge; antenne, apex of posterior tibie, and basal joint
of posterior tarsi rosaceous; eyes black; pronotum and
scutellum with a central pale longitudinal line; head with a
narrow, profound, central, longitudinal incision between eyes ;
basal joint of antenne: moderately incrassate and about as
long as head, second joint about as long as posterior tibia,
slightly longer than third; pronotum very finely and obscurely
granulate, its posterior margin concavely sinuate, the meso-
notum exposed ; antenne not pilose ; basal joint of posterior
tarsi very long.
Long. 5 mm.
270 Mr. W. L. Distant on
Megacelum modestum, sp. n.
Very pale ochraceous, with a slight virescent tint; basal
joint of antennee and anterior and intermediate femora dark
ochraceous, apical areas of posterior femora pale reddish
castaneous; eyes, apices of rostrum and scutellum, and
sometimes the central subbasal margin of pronotum piceous ;
membrane greyish, opaque ; basal joint of antenne a little
incrassate and slightly longer than head, remaining joints
much more slender but about equally thick, second joint
shorter than posterior tibia; head with a distinct linear
incision between the eyes; rostrum about reaching the
posterior cox ; posterior tarsi with the first joint shortest,
the third longest.
Long. 63 mm.
Megacelum townsvillensis, sp. n.
Ochraceous; legs, anterior callosities, and a large central
basal spot to pronotum, cuneus, and membrane black ; corium
slate-black, with the lateral margins widened into an oblong
spot near apex, ochraceous; lateral margins and apex of
cuneus pale castaneous ; antenne ochraceous, extreme apex
of first joint (sometimes concolorous) and apex of second
joint black, apex of third and the whole of fourth (excluding
base) fuscous; legs stramineous, femora ochraceous, apices
of tarsi black ; first joint of antenne a little longer than head,
second and third subequal in length; head with a distinct
central longitudinal impression between eyes; pronotum very
finely and obsoletely transversely wrinkled; scutellum
moderately tumid; posterior tarsi with the first joint
shortest, third longest.
Long. 73 mm.
Megacelum suffusum, sp. n.
Dull dark ochraceous; head, antenne, extreme margins
of pronotum, scutellum, narrow lateral margins to corium,
and legs pale ochraceous ; eyes, pronotum (excluding extreme
margins), a large central spot to scutellum, basal and apical
streaks to clavus, sublateral basal streak and transverse
apical fascia to corium, apical halves of posterior femora, the
posterior tibize, and apices of tarsi black; first joint of
antennz and anterior and intermediate legs mottled with
fuscous; apex of second joint, subapical fascia to third joint,
and fourth joint of antennz (excluding base) black; cuneus
pale castaneous; second joint of antenna a little longer than
third; pronotum coarsely transversely rugulose; scuteilum
Heteroptera from North Queensland. 271
somewhat foveate at base ; posterior tarsi with the first joint
shortest, third longest.
Long. 6 mm.
Division CYLAPARIA.
VOLKELIUS, gen. nov.
Head short, broad, transverse, abruptly deflected in front
of eyes, broadly centrally sulcate on basal area, with eyes
very much broader than anterior margin of pronotum;
rostrum reaching the anterior coxe ; antenne strongly pilose,
with the first joint strongly incrassate, shorter than head,
second joint about as long as head and pronotum together,
more slender than first, but distinctly clavate at apex, third
about as long as pronotum, incrassate, attenuate towards
base, fourth incrassate, shorter than third, and narrowed at
base and apex ; pronotum rugosely punctate, with a narrow
anterior collar and two transverse callosities before middle,
a little tumid and convex posteriorly, and deflected anteriorly,
basal margin about three times broader than anterior margin,
lateral margins almost obliquely straight, lateral angles
rounded but not prominent, posterior margin slightly con-
cavely sinuate before scutellum, which is tumid, subtriangular,
and profoundly, centrally, longitudinally sulcate ; lateral
margins of the corium carinately reflexed ; cuneus longer
than broad ; membrane with a single oblique basal cell;
legs pilose, femora a little thickened, posterior tarsi with the
first and second joints almost subequal in length, third a
little longest ; connexivum exposed, with the posterior
segmental angles prominent.
Allied to the West African genus Sahlbergella, Haglund.
Volkelius sulcatus, sp. n.
Reddish ochraceous; antenne (excluding extreme base),
eyes, scutellum, lateral margins (widened posteriorly) and
inner apical margins of corium, membrane, spots to con-
nexivum, and legs black; anterior and intermediate tibiz
(excluding base) and the tarsi (excluding apex) pale ochra-
ceous ; a minute pale spot to membrane near apex of cuneus;
pronotum rugulosely punctate; scutellum granulate, pro-
foundly centrally sulcate.
Long. 73-84 mm.
Eucerocoris suspectus, sp. n.
3. Pale reddish ochraceous; antenne, eyes, a central
272 Mr. W. L. Distant on
annulation to posterior femora, bases of tibie, and the tarsi
black or piceous ; corium fuscous, its base, about basal half
of lateral margin, and a spot near apical inner angle pale
reddish ochraceous; membrane pale fuscous; legs (excluding
black markings) ochraceous.
?. Reddish or pale sanguineous ; head and antenne black ;
legs and abdomen beneath pale ochraceous; apical half of
abdomen (excluding segmental margins), apical halves of
femora, basal annulation to posterior femora, basal areas
of tibie, and the tarsi black ; corium dull purplish black, its
base reddish ochraceous; membrane pale fuscous.
Head broad, deflected in front of eyes, with a distinct
angulated tubercle near the inner margin of each antenna, a
distinct, narrow, central, linear sulcation, eyes projecting con-
siderably beyond anterior margin of pronotum ; antenne not
hirsute, with the first joint thickened and clavate at apex,
about as long as posterior tibiae; remaining joints slender,
second a little longer than first; rostrum about reaching the
latitude of the intermediate coxe ; pronotum with two ante-
rior transverse impressions, the first defining a rather broad
collar, the second enclosing two transverse callosities, an
impression near each posterior angle which gives it the
appearance of being subprominent.
Long., ¢ 83, 9 94 mm.
As the species of the allied genus /elopeltis are well-
known destructive pests to tea- and other plantations, it is
probable that the species of Hucerocoris have similar habits.
Subfam. Capsrvz.
?
Division
ESTUIDUS, gen nov.
Subelongate ; head broad, deflected from shortly in front
of eyes, which project beyond the anterior margin of pro-
notum ; antenne with the first joint a little shorter than the
head but considerably passing its apex, second joint subequal
in length to posterior tibia and a little thickened at apex,
third and fourth joints very slender; rostrum reaching the
intermediate coxe ; pronotum with the posterior about twice
as broad as the anterior margin, its lateral margins sinuate,
provided with a very narrow anterior collar, compressed
before middle where it is strongly callose, immediately behind
the constriction is a distinct discal foveation variable in size ;
scutellum moderately tumid, foveately suleate at base; corium
and clavus distinctly punctate, a distinct foveation at suture
Heteroptera from North Queensland. 273
of corium behind claval apex; cuneus considerably longer
than broad, its apex acute; membrane with a single elongate
basal cell; legs of moderate length, femora very slightly
thickened.
I place this genus near Malalasta, Dist., Malacopeplus,
Kirk., and Gutanerius, Dist., which will probably assist to
constitute a distinct division of the subfam. Capsinee.
“stutdus foveatus, sp. n.
Ochraceous ; scutellum stramineous ; antenne, eyes, clavus
(excluding base), a large subrotundate spot on posterior
disk of corium, membrane, upper surfaces of femora and
anterior tibize, the intermediate and posterior tibize, and the
tarsi black ; extreme base of first joint of antennz ochraceous,
third and fourth joints fuscous; legs finely setose; body
above finely pilose, clavus and corium distinctly and some-
what coarsely punctate, cuneus pale with the margins and
apex slightly fuscous; pronotal discal foveation broad and
profound; scutellum glabrous, its basal sulcation linear but
situate in a distinct foveation.
Var. Clavus wholly black.
Long. 7 mm.
Estuidus marginatus, sp. .
Very pale ochraceous or stramineous; eyes, scutellum,
clavus, inner area of corium, membrane, and first and second
joints of antenne black or piceous; third and fourth joints
and extreme base of first joint of antennz ochraceous; body
above shining, membrane opaque with its margins hyaline ;
pronotal discal foveation less pronounced than in the pre-
ceding species; clavus and inner area of corium very finely
aud somewhat obscurely punctate; legs finely and obscurely
setose.
Long. 74 mm.
Division CAPSARTA.,
Lygus flavoscutellatus, sp. n.
Dark shining ochraceous, body beneath much paler; scu-
tellum and cuneus stramineus, the last with a small dark
apical spot; eyes and apices of the tarsi piceous; antennz
with the third and fourth joints and the apex of the second
joint fuscous, first joint a little shorter than head, second sub-
equal in length to posterior tibize ; pronotum very finely and
obscurely granulate; scutellum glabrous; corium finely
obscurely pilose and obsoletely finely granulate; apical areas
Ann. & Mag. N. Hist. Ser.7. Vol. xiii. 18
Die Mr. W. L. Distant on
of posterior femora speckled with bright pale castaneous ;
tibize darkly setose; rostrum about reaching the posterior
coxz, its apex black.
Long. 33-4 mm.
Peciloscytus antennatus, sp. n.
Piceous, thickly greyishly pilose, disk of pronotum and
scutellum somewhat castaneous; cuneus bright pale casta-
neous, its basal and apical margins very narrowly ochraceous;
membrane fuscous ; antenne pale ochraceous, the first joint
and apex of second piceous, fourth joint fuscous ; legs
piceous, anterior and intermediate tibiz (excluding base),
about apical third of posterior tibiz, and tarsi (excluding
apex) pale ochraceous ; pronotum with two small, obscure,
anterior discal black spots, and its posterior margin very
narrowly ochraceous ; first joint of antennz shorter than head,
second about as long as posterior tib’e, third and fourth
almost subequals in length ; ; coxe dull red.
Long. 34-45 mm.
In this species the eyes are very large and constitute a
rather aberrant feature of the genus.
Peciloscytus flavipes, sp. n.
Black, shining, finely sparingly greyishly pilose ; basal
margin of head, : antenne, rostrum, coxee, and legs very pale
ochraceous 5 apical areas of posterior femora reddish ochra-
ceous; third and fourth joints and apex of second joint of
antenna, apex of rostrum, and apices of tarsi piceous ; cuneus
castaneous, its anterior and posterior margins narrowly
luteous; membrane fuliginous with paler suffusions ; first
joint of antenne shorter than head, second about as long as
posterior tibiz ; eyes large and prominent, but smaller than
in the preceding species; pronotum granulate; posterior
femora moderately thickened.
Long. 23-3 mm.
Camptcbrochis signatus, sp. n.
Ochraceous ; apex of second joint of antenne, eyes, a
broad central longitudinal fascia to scutellum, and a broad
fascia at incisural margins of clavus black ; first, third, and
fourth joints of antennee, inner apical area of corium, central
and subapical annulations to posterior femora, apices ‘of tarsi,
lateral areas of sternum, lateral and central areas of abdomen
(imperfectly seen on carded specimen) fuscous ; membrane
pale brownish ochraceous, the venation fuscous ; ; first joint
Lleteroptera from North Queensland. 275
of antenne very slightly thickened and almost as long as
head, second joint subequal in length to posterior tibiee ; pro-
notum somewhat coarsely punctate, corium more finely punc-
tate (except on lateral marginal areas, which are impunctate).
Long. 44 mm.
Division BRYOCORARIA.
FINGULUS, gen. nov.
Body short, broad, convex, shining ; head somewhat long,
its base distinctly constricted and transverse; clypeus very
prominent, compressed, subconical above, and conyexly de-
pressed ; eyes of moderate size, situate much nearer to base
of antennz than to posterior margin of head, a very distinct
lateral callosity at their hinder margins; antennze with the
basal joint subglobosely incrassate, a little shorter than head,
second joint of ordinary thickness, more slender at base, and
very slightly thickened towards apex, subequal in length to
posterior tibiz, third and fourth joints slender, third longer
than fourth ; rostrum imperfectly seen, owing to typical
specimen being in a carded condition; pronotum convex,
coarsely punctate, strongly deflected anteriorly, with a pro-
minent ridged anterior collar, width between pronotal angles
(which are subprominent) about four times that of anterior
margin, lateral margins almost obliquely straight ; scutellum
subtriangular, sparingly coarsely punctate ; lateral margins
ot the hemelytra a little convexly ampliately depressed, clavus
and corium somewhat thickly punctate, cuneus opaque, im-
punctate, about as broad at base as long; membrane with
two short basal cells; legs of moderate length, anterior and
intermediate femora moderately thickened, posterior femora
more strongly incrassate, apical joint of tarsi moderately
thickened.
This genus may be provisionally placed near Physetonotus
of the Neotropical region.
Fingulus atroceruleus, sp. n.
Shining indigo-black ; second joint of antennz (excluding
apex), apical halves of tibiz, and the tarsi pale ochraceous;
third and fourth joints of the antennz fuscous, the extreme
base of third pale ochraceous ; cuneus slate-black, opaque ;
membrane pale hyaline, the basal area fuliginous ; body
beneath black, imperfectly seen owing to the typical specimen
being “carded.”
Long. 8 mm. a
18%
276 On a new Fish from the New Hebrides.
Synonymical Notes on Australian Species.
Fam. Pentatomide.
Philia regia.
Philia regia, Bergr. Proc. Roy. Soe. Victoria, vii. p. 287 (1895).
Philia leucochaicea, Bredd. Societas Entomol. xvii. p. 58-(1908).
Thilia crea.
Philia erea, Dist. ‘ Entomologist,’ Suppl. xxv. p. 96 (1892).
Philia compacta, Bredd. Societas Entomol, xvii. p. 57 (1903).
Dr. Bergroth drew my attention to the synonymical aspect
of these two species.
Fam. Reduviide.
Genus CROSCIUS.
Croscius melanopterus, Stal, En. Hem. iv. p. 80 (1874).
Castruccius insignis, Dist. Ann. & Mag. Nat. Hist. (7) xi. p. 356
(1903).
As Stal only gave indications of this genus in his “ Con-
spectus generum”’ and placed it in a position of the sub-
family Acanthaspine which I think it should not occupy,
I have hitherto failed to recognize it, and, what is worse,
have redescribed it. Its place seems clearly near Staliastes.
XXXIV.— Description of a new Fish of the Genus Cheetodon
jSrom the New Hebrides. By C. TATE ReGcan, B.A.
Chetodon Dixon.
Depth of body 13-13 times in the total length (without
caudal), length of head 3} times. Snout as long as the eye,
the diameter of which is 3 times in the length of head and
greater than the interorbital width. Scales very large on
the sides, becoming quite small posteriorly, about 30 in a
longitudinal series. D. XIII 21-22, the anterior spines
stout, increasing in length to the fowth or fifth, the soft fin
rounded. <A. III 16-17, the third spine slightly longer
than the second, longer than the longest dorsal spine and
nearly as long as the head, the soft fin pointed. Pectoral
nearly as long as the head. Ventral extending to origin of
anal. Caudal scarcely emarginate. Anterior 3 of body,
with spinous dorsal and anterior 4 of anal, greyish ; posterior
part of body, with soft dorsal, caudal, and posterior } of anal,
yellow. A vertical dark brown ocular band, narrower than
On new Hymenoptera from Northern India. 277
the eye, meeting that of the other side above and extending
to the margin of the suboperculum below; a brown area
below the anterior part of spinous dorsal; some dark stripes
extending downwards from the spinous dorsal, running some-
what obliquely backwards below the middle of the side, and
with a darker spot on each scale; anterior part of anal
becoming blackish towards its tip; soft dorsal, caudal, and
anal with a blackish intramarginal line; a faint dusky blotch
on the anterior part of the soft dorsal; a faint dark bar across
the base of caudal.
Total length 85 mm.
Two specimens, collected and presented to the British
Museum by Lieut. Kenneth Dixon, R.N,
This species is closely allied to C. vanthurus, Blkr., and
C. Mertensit, C. & V., from both of which it is distinguished
by the deeper body and more pointed anal fin, as well as
by the ocular band without light edges and other details of
coloration. |
XXXV.—On some new Species of Hymenoptera from
Northern India, By P. Cameron.
Tue species described in this paper are from the Khasia
Hills, Assam, and Simla, and are in the collection of Mr.
G. A. James Rothney.
278 Mr. P. Cameron on new
Ichneumonide.
Hadrojoppa fumipennis, sp. n.
Black ; the face, except for an irregular mark in the centre
(it is joined to the base of the antenne by a narrow line,
and there is a shorter line on either side), the inner orbits
(narrowly below, more broadly above, and the line extends
slightly beyond the top of the eyes), the lower half of the
outer entirely, with a narrow line above, a line on the pro-
notum, tegulze, two short lines on the centre of the mesonotum
(obliquely narrowed on the inner side), the scutellums, two
large triangular marks on the sides of the metanotum
(laterally extending on to the pleurz), a large mark on the
lower half of the mesopleurz (broadest at the base), an irre-
gular mark (narrowest at the base) on the centre of the
metapleurz, the apical half of the postpetiole, and two large
irregular marks on the apex of the second segment, pale
yellow. Legs pale yellow; the four front femora behind
and at the base and apex in front, the hind coxe below and
on the inner side, the base of the femora narrowly, the
apical third, the base of the hinder tibize narrowly (their apex
more broadly), the apices of the basal three joints of the
tarsi, and the apical entirely, black. Wings smoky, with a
violaceous tinge ; the nervures and stigma black. @?.
Length 20-22 mm.
Antenne ringed with white before the middle, fuscous
beneath towards the apex. Face and clypeus closely punc-
tured and thickly covered with white pubescence. Front
closely punctured. Mesonotum and scutellum closely, the
pleure Jess closely, punctured; the median segment more
closely and strongly and more thickly covered with white
pubescence. Areola twice longer than broad, roundly
narrowed towards the base, the apex broadly curved inwardly ;
irregularly finely rugose, the apex with a broad, smooth,
shining border. Postpetiole in the middle closely longitu-
dinally striated, the second to fourth segments closely punc-
tured, the apical smooth and shining. Gastroceeli large,
deep, broad, smooth, except for a few strie; the space
between strongly striated.
The described Khasia species of this genus may be sepa-
rated by the following table :—
1 (4). The petiole only marked with yellow.
2 (8). Large; the areola distinctly longer than broad, its
apex broad, smooth, transverse, the yellow line
on the petiole dilated backw ards ; the autenne
stout: dlengthi.27 amy. ~ o..<). sds lcemaeeeaenee forticornis,
Llymenoptera from Northern India. 279
3 (2). Medium-sized; the areola not distinctly longer
than broad, its apex not transverse; the yellow
line on the petiole not dilated backwards; the
antennee not stout. Length 17 mm........... maculiceps.
4 (1). The second or following segments marked with
yellow.
5 (6). The second segment with two yellow marks, the
others immaculate ; the areola sharply narrowed
MeUD NEY ESO Meciaia: cis. ees tain eaene fee y Coy os Sumipennis.
6 (5). The second segment broadly yellow at the apex;
the third and fourth segments with two large
marks on the apex; the areola broadly rounded
PMR EMER AS Oe cack cx ct norte hn ai caiiscs a: 6 As veio he annulitarsts.
Mutillide.
Mutilla inoa, sp. n.
Black, densely covered with silvery pubescence ; the second
and third abdominal segments ferruginous; the scutellum
pyramidal, its basal slope smooth and shining in the middle ;
the basal area on the median segment of equal width
throughout and reaching to the top of the apical slope; the
wings fusco-violaceous, paler at the base. ¢.
Length 15 mm.
Antenne black, the scape covered with white hair. Head
rugosely punctured, with a smooth space on the sides of the
ocelli; the front and occiput thickly covered with long white
hair, the vertex more sparsely with longer black hair. Face
and clypeus bare, smooth and shining, the apex of the clypeus
transverse and clearly separated from the sides. Base of
mandibles thickly covered with silvery pubescence; the sub-
apical tooth distinct. The malar space ends in a tubercle or
blunt rounded tooth on the inner and outer side. Pronotum
thickly covered with silvery pubescence ; on the basal slope
is a central and two lateral smooth spots; the propleure
rugosely punctured, the apex smooth, the middle depressed
and obscurely stoutly striated. Mesonotum rugosely punc-
tured and thickly covered with longish black hair. Scutellum
pyramidal, rugose, the basal slope smooth and shining; the
base and apex of the smooth part longitudinally furrowed ;
the apical slope is oblique; the basal is also oblique, but
more rounded than the apical; the hair is long, on the basal
slope black, on the apical fuscous. Median segment coarsely
reticulated, the base thickly covered with depressed silvery
pubescence ; the central area is of equal width throughout.
Metapleurz (except in the centre) reticulated. The second
and third cubital cellules at the top are about equal in length.
Abdomen black ; the extreme apex of the first and the whole
280 Mr. P. Cameron on new
of the second and third segments ferruginous ; the pubesence
is white, on the apical two segments black; the pygidium
rugosely punctured, with a smooth space, dilated at the base
and apex in the middle. The ventral keel with a slight
broad curve. The epipygium is smooth at the base; the
rest depressed, irregularly rugose, with the sides smooth and
raised. The apex of the radius is straight and oblique and
distinct from the lower part. Thesecond abdominal segment
is punctured, smooth in the centre; above it is gradually
rounded.
Comes near to M. perdita, Cam.
Mutilla artaxa, sp. n.
Length 15 mm.
Hab. Sila.
This species agrees so closely in form, coloration, and
structure with M. inoa that it might be considered identical
with it, if it were not for the difference in the form of the
ventral keel and of the pygidium. The two may be separated
thus :—
The ventral keel slightly narrowed in the middle; the
smooth space on the pygidium V-shaped (broad at
the base, becoming gradually wider towards the apex),
narrow, the sides'siraight(3).\cnid. aielvtian amadtete sts wnoa.
The ventral keel broadly projecting downwards at the
base, forming a large triangular tooth ; the smooth
space on pygidium large, broader at the apex than
at the base; the sides curved inwardly at the base
an@iapex Rina ee we ee Se: SA eee ees artaxa, Cam.
The form of the scutellum is the same, but in artava the
smooth space is not furrowed ; the basal area on the median
segment is the same; the apical abscissa of the radius is
gradually rounded, and does not form two parts, as in inoa.
Mutilla trebia, sp. n.
Black; the basal segment of the abdomen and the second
(except at the apex) dark red, the second at the apex covered
with black, the third, fourth, and fifth with white pubescence.
Wings fuscous violaceous, the second segment with an oblique
slope on the basal half. o.
Length 15 mm.
Head rugosely punctured above the antenne; the front
and cheeks thickly covered with long silvery hair; clypeus
smooth and bare. Prothorax rugosely punctured; the ape
ITymenoptera from Northern India, 281
of the propleure smooth; the mesonotum rugosely punc-
tured, with two longitudinal furrows, and covered with dark
fuscous hair. Scutellum more coarsely rngosely punctured,
thickly covered with long pale hair, and not raised above the
level of the mesonotum. Median segment coarsely reticu-
lated ; the central area short and wide, its base not twice its
length, its apical half narrowed. Propleurz punctured, except
at the apex ; the mesopleure punctured, except at the base and
apex; the metapleure with one row of large reticulations
on the apex, the lower middle part with some large round
punctures. The hasal two abdominal segments are dark red ;
the apex of the second black and covered with black hair; the
ventral keel is almost straight and the apex is oblique and
forms an incision with the obliquely rounded base of the second
segment. The second segment is obliquely depressed from
the middle on the basal and apical slopes; the white pubes-
cent bands on the third, fourth, and fifth segments are
broad ; the pubescence on the apical segment is black.
This species is not unlike pandara, Cam.; that is a more
slenderly built species and is smaller.
FossoreEs.
TYPHTA.
i. Median segment with three keels,
A. The first transverse median nervure placed distinctly behind the
basal, which is curved and thickened before the cubital nervure; a
stout keel, broad and square at the base, extends on to the middle of
the ventral surface of the petiole.
Tiphia clavinerva, sp. n.
Nigra ; abdominis apice dense fulvo-piloso ; alis fere fulvo-hyalinis,
nervis fuscis, stigmate nigro. <d.
Long. 9 mm.
Scape of antenne sparsely covered with long fuscous hair;
aciculated, sparsely punctured, shining ; the flagellum opaque,
thickly covered with pale down. Front and vertex shining,
strongly punctured, more sparsely laterally below the ocelli,
Face and clypeus closely punctured, thickly covered with
fuscous pubescence; the apex of the clypeus has a rounded
incision. Mandibles shining, rufous before the middle, the
base sparsely covered with pale and golden hair ; palpi rufo-
testaceous. Pronotum sparsely punctured on the basal half,
shining ; the base thickly covered with long pale fuscous
282 Mr. P. Cameron on new
hair. Mesonotum punctured, more sparsely and irregularly
on the sides, and thickly covered with short fuscous puabes-
cence. Scutellum punctured like the mesonotum; post-
scutellum more closely and finely punctured. The middle of
the metanotum bears three parallel keels ; the space enclosed
by them is strongly irregularly aciculated ; the sides are
closely striated ; the apex is strongly aciculated and. thickly
covered with a pale pubescence ; ‘the top is depressed and
longitudinally striated. Propleurze smooth and_ shining ;
the base below strongly aciculated. Mesopleurz sparsely
punctured and thickly covered with pale pubescence. Meta-
pleuree striated (except at the base, which is strongly acicu-
lated). Prosternum largely roundly tuberculated laterally
on the apical half; the middle depressed. Mesopleure with
two curved divergent furrows; the space between at the apex
depressed in the middle. Legs thickly covered with white
hair; the fore femora and tibiz and the middle tibiz less
broadly rufous. Abdomen shining; the third and following
segments thickly covered with bright fulvous pubescence ;
before the apex of the petiole is a narrow, longitudinally
striated, transverse furrow; on the base of the second
segment is a deeper, more regularly striated furrow ; the
apical segments are strongly punctured; the pygidium is
smooth down the middle. Beneath, the base of the petiole
is strongly aciculated, opaque, sharply keeled at the base
and less “strongly down the sides ; the apex is more strongly
obliquely raised ; in front of this is a stout strongly acicu-
lated keel which reaches near to the middle, becoming
narrower and smoother as it does so; the middle is sparsely
punctured; the apical half very smooth and shining ; the
second ventral segment is sparsely, the others more closely
and distinctly, punctured and thickly covered with fuscous
hair, The transverse median nervure is received distinctly
behind the transverse basal ; the apex of the radius is roundly
curved ; the second transverse cubital nervure is straight,
oblique ; the third is rounded outwardly at the top and
oblique below ; the second recurrent nervure is received in
the middle of the cellule.
LB. The first transverse median nervure not placed distinctly behind the
basal; the petiole without a stout keel on its ventral surface.
Tiphia himalayensis, sp. n.
Black, densely covered with longish dark silvery pubes-
cence ; the pro- and metapleurée closely obliquely striated ;
Hymenoptera from Northern India. 283
the wings fuscous violaceous, the second transverse cubital
nervure roundly bisinuate. ?.
Length 15-16 mm.
Front and vertex coarsely punctured, more sparsely on the
ocellar region; the clypeus closely punctured, its apex
smooth and broadly rounded. Mandibles broadly piceous.
Middle of pronotum strongly punctured; the apex smooth,
the basal slope closely punctured. The middle of the meso-
notum is strongly punctured; the sides are sparsely punc-
tured. Scutellum sparsely and deeply punctnred on the
base and apex; the postscutellum is sparsely punctured.
Median segment 3-keeled, opaque, strongly aciculated,
smoother, more shining on the sides at the apex, and irregu-
larly striated near the bordering keel. The apical slope is
coarsely aciculated. Pro- and metapleuré closely obliquely
striated, the mesopleurz strongly and closely punctured.
Wings uniformly fuscous violaceous and highly iridescent ;
the second transverse cubital nervure is roundly curved out-
wardly above and below, the upper part more roundly and
distinctly than the lower. The tibiz and tarsi are thickly
covered with dark silvery hair; the spines are rufous.
Abdomen shining; the apical, dorsal, and the ventral
segments thickly covered with long silvery hair; the basal
half of the pygidium is thickly haired; in the middle is a
longitudinal keel.
Tiphia robusta, sp. 0.
Black ; the hinder femora bright red; the wings dark
fuscous violaceous, the nervures and stigma black. 2.
Length 15 mm.
Head above the antennee coarsely and strongly punctured ;
there is a smooth patch behind each of the hinder ocelli and
a smooth line down the front in the centre ; the apex of the
elypeus smooth. Mandibles black, dull rufous beyond the
middle. The apex and the basal slope of the pronotum
smooth, the middle strongly but not very closely punctured.
The centre and sides of the mesonotum are rather strongly
but not closely punctured ; the scutellum is similarly pune-
tured on the sides and apex ; the postscutellum is punctured
laterally. Median segment 3-keeled, opaque, aciculated ;
the outer keels converge slightly near the apex ; the central
keel becomes thinner towards the apex. Propleurz smooth,
with a few indistinct scattered punctures ; the mesopleure
closely and strongly punctured; the metapleure closely
striated, except at the base below. Legs black, the hinder
femora bright red; the tibize and tarsi are covered thickly
284 Mr. P. Cameron on new
with white hair; the calcaria black. Wings dark fuscous
violaceous ; the nervures and stigma black. Abdomen black,
shining, finely punctured, the apical segment thickly covered
with long black hair, except on the apex; the ventral seg-
ments are fringed with white hair.
Comes near to 7. rufofemorata and T. khasiana, but these
species are both smaller and have the middle femora red.
The upper half of the second transverse cubital nervure is
roundly curved outwardly.
Tiphia denticula, sp. n.
Long. 12mm. o. ,
This species comes near to 7. canaliculata, but is more
slenderly built ; the depression on the apex of the median
segment is not so wide nor so deep, nor is it so regularly
striated ; the basal abscissa of the radius is distinctly angled
above the middle, not gradually rounded as in canaliculata ;
the lower abscissa of the apical part of the radius is longer,
and there is a more distinct angle formed by it with the
second recurrent nervure.
Head opaque, closely rugosely punctured and_ thickly
covered with long white soft hair; the front is indistinctly
keeled in the middle. Clypeus closely rugosely punctured,
its apex smooth and transverse. Mandibles black, as are
also the palpi. Pro- and mesonotum shining, closely punc-
tured (except on the apex of the former) ; the scutellum and
postscutellum are similarly punctured. Median segment
irregularly coarsely aciculated ; the three keels extend to the
apex, but the outer become weaker towards the apex, which
is broadly depressed, shining, and bears a stout longitudinal
keel in the centre. The apical slope is coarsely aciculated
and keeled down the middle. The basal half of the pro-
pleure is aciculated and obscurely striated ; the mesopleuree
strongly and closely punctured ; the metapleure striolated,
aciculated at the base. Wings uniformly fuscous, with a
violaceous tinge ; the nervures and stigma black ; the trans-
verse basal nervure is thickened near the top, the transverse
median is received shortly behind it; both the recurrent
nervures are received shortly beyond the middle. There is a
distinct curved broad tooth on the underside of the petiole
at the base, from which a keel runs to the middle. The
hair on the apical and on the ventral segments is long and
white,
Hymenoptera from Northern India. 285
Ziphia tuberculata, sp. n.
Nigra, mandibulis rufis, tarsis testaceis ; alis fusco-hyalinis, nervis
fuscis, tegulis rufis ; basi petioli subtus tuberculata. 2.
Long. 8 mm.
Antenne black, the apical joimts rufous beneath; the scape
is finely and closely punctured above, the sides and lower
side covered with long silvery hair; the base of the flagellum
is sparsely covered with white hair; the rest of it bears a
white pubescence. The front is closely punctured below,
more sparsely above ; the vertex is similarly punctured ; both
are thickly covered with long fuscous hair; the clypeus
smooth, shining, punctured closely at the base, its apex
rounded. Mandibles red, black at the apex; their underside
fringed with long golden hair. Palpi testaceous, the apical
joints paler. Pronotum coarsely punctured, its apex smooth,
the basal slope finely and closely punctured. The middle of
the mesonotum is strongly but not closely punctured, its
base and sides smooth, bare ; the base in the middle slightly
depressed. Scutellum strongly punctured (except in the
middle) ; the postscutellum finely punctured. Median seg-
ment strongly aciculated; the three keels are almost parallel
and all reach to the apex; the space bounded by them has a
blistered appearance; the apex at the sides is depressed and
bears a few striz ; the apical slope is blistered, is thickly
covered with a white pubescence, and is obscurely keeled
down the middle. The top of the propleurz is smooth, the
rest obscurely punctured; below the middle is an oblique
keel. Mesopleurz closely punctured, the apical slope strongly
aciculated ; the pubescence is thick and pale. Metapleurz
closely striated, much more finely, almost strongly aciculated
on the base below. Mesosternuin sparsely punctured,
shining ; the hair long and fuscous; the apical area is trian-
gular at the base ; finely furrowed down the middle, the apex
in the middle triangularly depressed. Legs black ; the fore
knees, the apex of the tibize, and the tarsal spines rufous ;
the tibial spines are pale. The second transverse cubital
nervure is roundly curved outwardly in the middle ; the first
recurrent nervure is received shortly, but distinctly, before
the middle of the cellule and is roundly curved above; the
second is received close to the apical third of the cellule.
Abdomen shining, sparsely punctured, the middle and apical
segments thickly covered with long white hair; the base of
the second segment is depressed and marked with longitu-
dinal keels all over; the apical half of the pygidium is rufous
286 Mr. P. Cameron on new
and smooth. The petiole beneath issmooth; the base punc-
tured closely ; its middle with a blunt raised tooth ; its basal
slope is longer, more rounded than the apical, which has an
oblique slope.
Comes near to T. spinosa, but is smaller; the median
segment is not transversely striated in the middle ; the tooth
on the petiole is blunter and longer ; the under surface of
the petiole at the apex is smooth and shining ; the top of the
propleurze smooth and shining, and the ‘mandibles are
rufous.
Tiphia fulvinerva, sp. n.
Nigra, albo hirsuta, propleuris striolatis ; metanoto opaco, medio
tres-carinato; alis fulvo-hyalinis, stigmate nigro, nervis fulvis. 2.
Long. 17 mm.
Scape of the antenne thickly covered with long white
hair; the second and third joints are smooth and shining,
sparsely covered with pale hair; the other joints are opaque
and thickly covered with a fulvous down. Front and vertex
bearing large, deep, clearly separated punctures, and with
long fuscous hair ; there is an elongated smooth space before
the ocelli ; above and between the antenne is a stout keel.
Clypeus closely punctured, its apex smooth and depressed.
Mandibles black, obscure rufous near the middle, their
lower side fringed with long pale golden hair. Palpi dark
testaceous. ‘The basal slope of the pronotum obscurely
punctured, smooth below; the basal half of the upper part
is strongly punctured, the apical smooth. Mesonotum
irregularly punctured, sparsely covered with fuscous hair ;
the scutellum has a few PTE Mas in the middle; the apex
has a row of large deep ones ; the sides are fee strongly
punctured. Propleuree closely striated; the basal keel
smooth and shining; the top with a row of punctures ; the
lower edge is opaque and strongly shagreened. Mesopleurz
strongly and deeply punctured and covered with long pale
hair. Metapleuree closely but not very strongly striated ;
the base opaque, shagreened. ‘The basal half of the meso-
sternum strongly and “deeply punctured, the apical smooth
and shining ; in its centre at the apex is a V-shaped area,
clearly bounded by deep furrows; it is widely furrowed
down the middle; the furrow is bordered by one or two
punctures ; its sides at the apex are triangular. Wings
fulvo-hyaline ; the nervures fulvous, the stigma darker ; the
apex of the radius is obliquely depressed and thickened ; the
first recurrent nervure is broadly rounded outwardly at the
TTymenoptera from Northern India. 287
top; the second is oblique and is received shortly beyond
the middle. Legs thickly covered with silvery hair; the
tibial and tarsal spines rufous. Abdomen shining; the
petiole with the punctures large ; the other segments have
them smaller and closer; the apical segments are thickly
covered with long pale hair; the pygidium has the basal
half black and strongly rugosely punctured ; the apical half
is for the greater part rufous; in its centre is a longitudinal
keel; on the sides are a few indistinct keels. The median
segment is strongly aciculated, opaque, and has in the middle
three keels ; the central reaches near to the apex, to which
it is joined by three minute ones ; the apex has an oblique
slope, is shagreened, opaque, and thickly covered with white
pubescence. The ventral segments are fringed with long
fulvous hair; the hypopygium is closely and strongly punc-
tured (except in the middle) at the apex. ‘The clypeus is
broadly rounded at the apex.
Comes into Bingham’s section B and 4? and 6°, but is
different from anything included therein. It might come
into section “C. Wings golden yellow,” but it is quite
distinct from 7. auripennis, the representative of the section.
Tiphia simlaensis, sp. n.
Nigra, capite pronotoque dense punctatis; metanoto opaco, dense
aciculato, medio bicarinato ; alis fusco-violaceis, nervis stigmateque
Mishisy/-~
Long. 12 mm.
Hab, Simla.
The scape of the antenne is covered with long white hair ;
the second and third joints are smooth, shining, sparsely
covered with white hair; the others are opaque and thickly
covered with a pale down, Front and vertex closely and
strongly punctured, more sparsely near the ocelli; they are
thickly covered with pale hair. The base of the clypeus is
closely and strongly punctured, the apex smooth and shining,
its middle roundly and distinctly incised. Mandibles smooth
and shining, their middle broadly rufous; palpi fuscous.
The lower part of the pronotum at the base is smooth and
shining, the upper finely and closely punctured; the top is
strongly and closely punctured (except on the apex).
Mesonotum shining and marked with widely separated large
punctures, ‘Lhe scutellum is punctured round the edges and
more sparsely in the middle ; the postscutellum is similarly,
but more closely, punctured; at its sides is an opaque, coarsely
aciculated depression. The basal region of the median
2838 Mr. P. Cameron on new
segment is opaque, coarsely aciculated, the sides near the
base finely striated ; the apex is smoother and more shining ;
there are two keels which reach to the apex and a less
distinct one which reaches on to the middle; the apex has a
blistered appearance, is sparsely, obscurely punctured, and
has an indistinct keel down the middle. The upper part of
the propleure is aciculated, the lower finely and closely longi-
tudinally striated; the middle of the mesopleure is closely
punctured and thickly covered with long white hair; the
apical half of the metapleure is strongly striated; the striz
are distinctly separated. ‘The basal half of the mesosteraum
is punctured; trom the middle, on either side, a curved
furrow runs to the sides at the apex ; the space bounded by
them is strongly punctured; outside them itis smooth. Legs
black, the hair white; the calcaria rufous, as are also the
tarsal spines. Wings uniformly fuscous violaceous, the
nervures and stigma black; the second transverse cubital
nervure is only slightly oblique and is roundly curved
above ; the second recurrent nervure is received at the base
of the basal third of the cellule. Abdomen shining; the
segments finely and sparsely punctured in the middle; the
apical segments thickly covered with long white hair; the
pygidium strongly punctured, the apex smooth, keeled in the
middle, depressed laterally.
Median segment with five keels.
Tiphia quinquecarinata, sp. 0.
Nigra, flagello antennarum, maudibulis, tarsis abdominisque apice
rufis ; al fulvo-hy alinis, nervis ruds, stigmate nigro. @.
Long. 11 mn.
Antenne rufous, the flagellum black above, thickly covered
with a pale down ; the scape black, shining, sparsely covered
with long white hair. Head shining ; the ‘front and vertex
punctured, but not very closely, and sparsely covered with
fuscous hair. Clypeus projecting; its apex rounded.
Mandibles rufous, black at the base, their underside fringed
with long golden hair; palpi testaceous. Thorax shining ;
the pronotum marked, but not closely, with large punctures,
its apex smooth. Mesonotum strongly and closely punctured
in the middle, more sparsely on the sides, and thickly covered
with fuscous hairs. Scutellum with a row of large punctures
round the apex, and there is a more scattered and irregular
row on the sides; postscutellum smooth, without punctures.
‘The three central keels on the median segment are parallel ;
Hymenoptera from Northern India. 289
the outer pair converge slightly towards the apex ; the central
hardly reaches to the apex; the two bordering it are dis-
tinctly separated from it; the space enclosed by the keels
is coarsely aciculated (except at the apex) ; the apex has a
sharp oblique slope, is strongly aciculated, and covered with
a pale down. Propleure shining ; the upper part smooth,
the lower very finely longitudinally striated ; the raised basal
edge is impunctate, very smooth, and shining. Mesopleure
shining, sparsely punctured in the middle, and covered with
white pubescence. The base of the metapleuree smooth at
the base, the rest closely striated. Mesosternum shining,
the basal two thirds sparsely, but distinctly, punctured ; the
apex smooth ; the apical area is triangularly narrowed at the
base, becoming gradually wider towards the apex; it is
almost opaque, sparsely punctured, and thickly covered with
short white hair; the middle furrow becomes triangularly
widened at the apex. The four anterior tarsi and the front
tibiz beneath are rufous; the hair on the four hinder tibiz
is Silvery ; the spines are rufous; the calcaria reddish tes-
taceous. Wings hyaline, with a fuscous tinge; the nervures
testaceous, the stigma black; the second transverse cubital
nervure is roundly curved outwardly on the upper half; the
lower part is straight, oblique. Petiole shining; the sides
and apex punctured; the punctured band on the apex
bounded at the base by a furrow ; the apices of the segments
are finely punctured and covered with pale hair; the pygidium
has the apical half rufous; the middle has a band of long
pale hair; the triangular apical part of the basal ventral
segment is very smooth, glabrous, and shining; the apex of
the hypopygium is testaceous and is covered with long fulvous
air.
In Bingham’s table this species comes into“ B. a’. Median
segment with five longitudinal keels.” 7. lyrata may be
separated from it by the apex of the petiole being longitudi-
nally striated ; the other species of the section (7'. flavipennis)
is easily known from it by the clypeus having two blunt
teeth on the apex.
Salius trichiosoma, sp. nu.
Niger, dense longe nigro pilosus; alis fusco-hyalinis, basi flavo-
hyalinis ; pedibus ferrugineis, basi late nigris. @.
Long. 22 mm.
Claws with one tooth. Antenne long, black, bare, mode-
rately stout. Head opaque, black, densely covered with
long black hair ; there is a narrow furrow on the front.
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 19
290 Mr. P. Cameron on new
Apex of clypeus transverse ; the labrum slightly projecting
laterally and to a less extent in the centre ; it is frmged with
long bright rufous hair. Mandibles and palpi black. Thorax
opaque, alutaceous, densely covered with long black hair ;
the pleure obscurely punctured and with a distinct oblique
furrow near the middle. ‘The apex of the median segment is
bare, smooth, and shining. Wings fulvous hyaline, the apex
with the fulvous tinge less well marked and with a violaceous
tinge. The stigma and costa are black; the nervures are
testaceous; the second cubital cellule is distinctly shorter
than the third above and below ; the third transverse cubital
nervure has the upper half straight and oblique, the lower is
not so oblique and broadly rounded. Legs rufo-testaceous,
the tarsi paler, the coxze, trochanters, and basal half of the
femora black. Abdomen smooth and shining.
A distinct species. Characteristic is the long, dense, black
hair on the head and thorax.
Salius Frederici, sp. n.
Black; the antennz (except at the base and apex) fulvous;
the tibize (except at the apex and the hinder tarsi) rufous;
the apices of the joints of the hinder tarsi black; the wings
flavo-hyaline, the base of the anterior dark smoky to the
transverse basal nervure, the hinder pair with the basal half
dark fuscous, the apical yellow. <6.
Long. 23 mm.
Claws with one stout tooth. Antenne as long as the body,
distinctly tapering towards the apex. Head black, sparsely
covered with long black hair; the mner orbits narrowly, the
face, clypeus, and labrum dark rufo-testaceous. A distinct,
deep, narrow furrow extends from the ocelli to the middle of
the front. Clypeus roundly convex ; its middle at the apex
transverse, the sides rounded. Mandibles black, the upper
part testaceous. The head is obliquely narrowed behind the
eyes and is well developed there; there is a testaceous line
on the outer orbits above. Thorax opaque, sparsely covered
with long black hair; the median segment is longish, has a
gradually rounded slope, and is obscurely transversely striated.
Wings yellowish hyaline; the base above is dark fuscous,
with a violaceous cloud to the transverse basal nervure, below
the cloud extends to the submedian nervure ; the second and
third cubital cellules are almost equal in length at the top
and bottom; the third transverse cubital nervure has the
upper half straight and oblique; the lower half is more
ITymenoptera from Northern India, 291
rounded. The four front tibize are darker coloured than the
hinder pair; the four front tarsi are almost entirely black.
Resembles in coloration S. anthracinus, Sm., but that
belongs to the group with bidentate claws.
Salius lugubrinus, sp. n.
Niger, pruinosus ; alis hyalinis, fusco-bifasciatis. 9.
Long. 7 mm.
Antenne slightly pruinose; the underside of the scape
thickly covered with short white hair. Front and vertex
almost bare; the face and clypeus thickly covered with silvery
pubescence ; the apex of the clypeus transverse, smooth, and
shining ; in the centre of the front is a narrow longitudinal
furrow. Apex of the mandibles reddish; the palpi black,
thickly covered with white pubescence. Thorax alutaceous,
shining; metanotum smooth; on its apex are two longish
depressions. Legs black, pruinose, more thickly at the base.
Wings hyaline; a large conical cloud extends from the base
of the cubital nervure along the transverse basal nervure to
the opposite side; there is a large cloud occupying the
greater part of the radial cellule, the middle cubital cellules,
and the middle of the discoidal cellules on either side of the
second recurrent nervure to near the edge of the wing; the
third cubital cellule is much narrowed above, being there
scarcely half the length of the second ; below it is slightly
longer ; the first recurrent nervure is received near the base
of the apical third, the second shortly, but distinctly, before
the middle. Abdomen smooth and shining, pruinose; the
hypopygium is thickly covered with long fuscous hair.
Pseudagenia lepcha, sp. un.
Blue, the hinder femora for the greater part red; the head
and thorax punctured and thickly covered with white pubes-
cence; the scutellum (except in the centre) closely longitu-
dinally striated; the median segment coarsely, irregularly
striated ; the wings fuscous hyaline, with a violaceous tinge ;
the nervures and stigma fuscous. 2? do.
Long. 13-15 mm.
Hab. Simla and Khasia.
Antenne black, the scape with a blue tint and covered
with a white pile. Front and vertex closely and distinctly
punctured; the clypeus, on the sides, bears some shallow
scattered punctures ; the raised centre is closely and distinctly
19%
292 Mr. P. Cameron on new
punctured; the parts above the antennz and behind the eyes
are thinly covered with long white hair, Mandibles black,
the base thickly covered with white pubescence. Palpi black.
Thorax blue, with purple and brassy tints; above it is closely,
but not very strongly, punctured ; the sides of the scutellum are
closely, irregularly, longitudinally striated; the postscutellum
towards the apex is irregularly transversely striated. Median
segment coarsely, irregularly, transversely striated ; there is
a broad shallow furrow down the middle. The hollowed part
of the propleure bears a few striz ; the mesopleure coarsely
rugose, the punctures running into oblique striz towards the
apex; the metapleure above closely, strongly, obliquely
striated, the base below is minutely punctured, the apex
coarsely closely reticulated. The four anterior legs are blue ;
the tibiz and tarsi darker coloured ; the hinder femora red,
narrowly purple at the base and apex. Wings uniformly
fuscous hyaline, highly iridescent and with a violaceous tint ;
the stigma and nervures are fuscous. Abdomen bright
metallic blue, very smooth, and shining.
Allied to P. blanda and P. prophetica, from both of which
it may be known by the strongly and closely punctured head
aud thorax, by the punctured and longitudinally striated
scutellum, and by the wings being not clear hyaline. The
head and thorax may have dark purple and brassy tints.
With the male the anterior femora and tibiz may be testa-
ceous 1n front.
Cerceris violaceipennis, sp. 0.
Black; the lower half of the inner orbits broadly, the antennal
keel, a reversed crown-shaped mark below it, a broad line on
the pronotum, the sides of the scutellum, the postscutellum,
the base of the petiole, the apical two thirds of the third
segment, and the apices of the following three segments
narrowly, rufous; the legs black, the apices of the four front
femora and the four anterior tibiz in front yellow; the wings
smoky, darker in front, the nervures and stigma black. ¢.
Long. 8 mn.
Scape of antennze for the greater part yellow; the base of
the flagellum broadly, the apex narrowly beneath, brownish.
Head closely and distinctly punctured ; the face and clypeus
thickly covered with silvery pubescence. Clypeus broadly
roundly projecting, the lower inner orbits, a large mark,
transverse at the base, becoming obliquely narrowed below
and ending in the middle in a rounded point, and the antennal
kecl are yellow. Thorax black; a broad band on the pro-
notum behind, the tegulz, the sides of the scutellum, and
4
Llymenoptera from Northern India. 293
the postscutellum reddish. The area on the median segment
is closely and uniformly punctured ; the rest of the segment
more strongly and deeply punctured all over. The segment
is more thickly and uniformly covered with fuscous pubes-
cence than the rest of the thorax. Abdomen closely punc-
tured ; the base of the first segment broadly, a small mark
in the centre of the second segment on the apex, the apical
two thirds or so of the third, and the apices of the three fol-
lowing segments narrowly red. Pygidium coarsely, but not
very closely, punctured. There is an elongated mark on the
sides of the second ventral segment and a small one on the
sides of the fifth.
The wings have a distinct violaceous tinge and are highly
iridescent. The fovez on the median segment are large; the
metapleuree are shining and only slightly punctured compared
with the mesopleure ; the propleure are stoutly obliquely
striated. In coloration the species agrees closely with C. b:-
maculata, Cam., but is abundantly distinct otherwise.
Cerceris latibalteata, sp. n.
Black ; a broad line, obliquely narrowed above, on the
lower inner orbits, the antennal kcel, the basal half of the
mandibles, a line on the hinder part of the pronotum, the
scutellum, postscutellum, the greater part of the third abdo-
minal segment, and a line on the apex of the fifth yellow;
the wings fuscous, the radial and the front of the cubital
cellules smoky ; the stigma and nervures black. ?.
Long. 7 mm.
Antenne black ; the flageilum broadly brownish beneath.
Head entirely black ; above the antennz closely punctured ;
the apex of the clypeus projects broadly, is transverse, and is
more shining than the face. The thorax is not strongly or
very distinctly punctured ; an irregular line on the apex of
the pronotum, the base of the tegule, and the scutellums are
yellow. The area on the median segment is shining, is
indistinctly finely punctured, aud has a narrow furrow down
the centre. Propleure obscurely striated ; the mesopleurze
punctured, and with a wide and deep longitudinal furrow in
the centre. Metapleurz shining, obsoletely punctured, and
obscurely striated under the wings. Legs black; the front
tibiz auteriorly and the tarsi yellowish. The greater part
of the third and the apex of the fifth segments are reddish ;
the pygidium irregularly shagreened and punctured.
294. Mr. P. Cameron on new
Larra bicolorata, sp. n.
Nigra, nitida, pruinosa ; femoribus posticis rufis ; alis fusco-violaceis,
stigmate nigro, nervis fuscis. ¢.
Long. 12 mm.
Scape of antenne and pedicle bare, smooth, and shining ;
the flagellum opaque, covered with a microscopic pubescence.
Head shining; the front and vertex bare, sparsely minutely
punctured; the ocellar region is depressed; the raised part
in front of the ocelli is furrowed down the middle; the
middle of the front is deeply furrowed ; the sides are more
broadly and not so deeply furrowed. Face and clypeus
closely punctured and thickly covered with pale pubescence ;
the labrum is fringed with long rufous hair. The base of
the mandibles closely punctured and covered with white
pubescence, the middle broadly rufous; the palpi black,
fuscous towards the apex, and thickly covered with white
pubescence. Pro- and mesonotum closely and distinctly
punctured and covered with a short down, having a fulvous
hue on the latter, which is broadly depressed in the middle
at the base and on the sides towards the apex. Median
segment closely and distinctly punctured on the sides, which
are slightly depressed ; the central part closely, transversely,
irregularly striated; the middle is slightly furrowed and
keeled down the centre of the furrow; the keel is fainter
towards the apex; the apical part has an oblique slope, is
closely punctured, the sides above transversely striated ; on
the apex are a few longitudinal striz ; the central furrow is
deep and extends to the top of the apical fourth of the seg-
ment. Propleurz closely punctured, obscurely striated in the
middle below; the mesopleurze are more distinctly punctured ;
the tubercles are large and depressed at the base; behind
they are bordered by a thick band of white pubescence ; the
basal perpendicular and the upper longitudinal furrows are
deep and obscurely striated. Metapleurze closely punctured.
Mesosternum closely and distinctly punctured, furrowed
down the middle, and there is a transverse furrow before the
middle coxe ; the metasternum is opaque, alutaceous, keeled
round the sides, the base and apex are rounded, there is a
distinct furrow down the middle. Wings fuscous violaceous ;
the first cubital cellule at the top is half the length of the
second; both the recurrent nervures are received behind the
middle of the cellule. Legs thickly pruinose ; the hinder
femora bright red; the tibiz and tarsi thickly spinose; the
tarsal spines and the claws rufous. Abdomen very smooth
Hymenoptera from Northern India. 295
and shining ; the apices of the segments pruinose ; the pygi-
dium has a few scattered punctures and hairs; the epipygium
is more closely and distinctly punctured and has a shallow
furrow on either side at the apex.
Larra pygidiahs, sp. un.
Nigra, femoribus posticis rufis ; alis fusco-violaceis, cellula cubitali
2* duplo longiore quam 1%. 9.
Long. 17-18 mm.
The scape of the antenne sparsely, the flagellum thickly,
covered with white hair; the second joint shining, sparsely
haired. Head shining, ‘the front sparsely punctured and
covered with white hair. The face and clypeus closely punc-
tured (except on the apex of the latter) and thickly covered
with white pubescence. The tooth of the mandibles and a
large space before their apex rufous, and fringed below with
long pale golden hair. The palpi brownish and thickly
covered with white hair. Pro- and mesonotum minutely
punctured; the mesonotum thickly covered with fuscous
pubescence. Median segment minutely punctured ; its
middle from the base to the top of the apical furrow closely
transversely striated. Pleurze shining ; the furrows on the
mesopleure distinct, the basal perpendicular one striated.
The metasternal area is thickly pilose; there is a central keel
which reaches to the apex and is much stouter at the base;
there is a narrower lateral keel which reaches to the middle
only. Legs thickly covered with white pubescence ; the
tarsal spines are rufous, as is also the base of the hinder
calearia; the hinder femora are red, black at the extreme
apex. The costa and stigma are black; the nervures are
fuscous ; the apical abscissa of the radius is very slightly
oblique ; the first cubital cellule is half the length of the
second ; the second recurrent nervure is roundly curved and
is received in the middle. Abdomen shining, pruinose;
the apices of the middle three segments depressed; the
pygidium sparsely haired ; strongly irregularly punctured, the
basal punctures smaller, those on the middle and apex almost
running into striz; the sides are furrowed; the outer edge
is sharply raised; the sides of the segments are punctured
(except below) and are sparsely covered with brownish hairs.
This is a larger species than L. bicolorata, with which it
agrees in coloration ; it may be known from it by the furrow
on the apex of the median segment not reaching to the apex,
nor originating at the top, by the middle of the basal part
296 Mr. P. Cameron on new
not having a keel, by the mesopleure not being so strongly
punctured, and by the abdomen being shorter compared with
the head and thorax—it being shorter than these united,
whereas in L. pygidialis it is distinctly longer.
Tachytes rufipalpis, sp. n.
Nigra, facie tibiisque dense aureo pilosis; abdomine argenteo
lineato ; alis flavo-hyalinis, nervis flavis, 9.
Long. 17 mm.
Scape of antennz densely covered with pale golden pubes-
cence; beneath aciculated and thickly covered with long
pale hair; the flagellum, especially at the base, thickly
covered with silvery pile. The vertex is closely and dis-
tinctly punctured and covered with long, soft, fuscous hair ;
behind the ocelli is a large semicircular, almost triangular,
deep depression ; round the inner side of the hinder ocelli
is a smooth shining keel, which is continued halfway down
the outer side of the ocellar region; the ocelli are placed
thus *.°; the face below the ocelli is thiekly covered with
bright golden pubescence; the clypeus is closely and dis-
tinctly punctured, its upper part thickly covered with
golden hair, its apex depressed, smooth, and shining. The
mandibles closely punctured at the base, opaque, the rest
smooth and shining; the palpi are rufo-testaceous. The
base of the pronotum bears a pale golden pile ; mesonotum
alutaceous and thickly covered with fuscous pubescence ;
the scutellum is more strongly and distinctly punctured.
Median segment thickly covered with long fuscous pubes-
cence, alutaceous. Pleurze alutaceous; the mesopleurz
thickly covered with golden pile and less thickly with
fuscous pubescence. Mesosternum closely punctured and
thickly covered with long pale pubescence; the area between
the middle coxe is keeled laterally and down the middle.
Legs densely pruinose; the tibiz thickly covered on the
outer side with bright golden pubescence; the tibial and
tarsal spines are bright rufous; the calcaria are dark
rufous, darker at the base. Wings yellowish, more hyaline
and without a yellow tint at the apex; the nervures are
bright yellow ; the upper two thirds of the first transverse
cubital nervure is roundly curved, the lower part is straight,
oblique; the first recurrent nervure is received at slightly
less than the length of the top of the second cubital cellule
from the first transverse cubital nervure, the second dis-
tinctly before the middle. Abdomen black, the basal four
segments broadly banded with silvery pubescence; the
Hymenoptera from Northern India. 297
pygidium is densely covered with bright golden stiff pubes-
cence ; the hypopygium is sparsely punctured near the apex;
the sides at the apex are stoutly keeled.
Comes near to 7, Saundersi in Bingham’s work, but is
abundantly distinct.
Tachytes assamensis, sp. n.
Nigra, palpis, femoribus dimidio apicali, tibiis tarsisque rufis ; alis
fulvo-hyalinis, nervis stigmateque rufis. 9°.
Long. 17 mm.
Antenne black; the scape beneath thickly covered with
long pale fulvous hair. The front, face, and clypeus
thickly covered with bright rufous pubescence and long
fulvous hair; the vertex alutaceous and covered with long
dark fulvous hair. Apex of clypeus bare, smooth. Man-
dibles with the basal half rufous above; the base thickly
covered with golden pubescence. Palpi rufo-testaceous.
Thorax thickly covered with longish bright rufous pubes-
cence, the pubescence on the pleure and breast sparser,
not hiding the colour of the skin; the hair on the scutellum
and median segment is longer. Legs rufous; the coxe,
trochanters, and base of femora black. The apex of the
wings want the yellowish tint; the radial cellule is infus-
cated; the first cubital cellule is slightly shorter than the
second; the first transverse cubital nervure is roundly
curved; the first recurrent nervure is received near tie
basal third, the second shortly beyond the middle.
Abdomen black, shining; the basal segment covered with
long dark fulvous hair; the apical and basal segments are
sparsely covered with long black hair; the pygidium thickly
covered with stiff rufous hair; the hypopygium has the
sides and apex punctured; the middle bare, smooth, and
shining.
Tachytes fulvo-pilosa, sp. n.
Nigra, dense aureo hirta; alis flavo-hyalinis, nervis stigmateque
flavis ; scapo antennarum dense aureo piloso. 9°.
Long. 20 mm.
Scape of antenne densely covered with golden pubes-
cence; the flagellum opaque, covered closely with a micro-
scopic pile. Head densely covered with bright golden
pubescence. Eyes converging above, where they are
separated by the length of the fourth antennal joint.
Clypeus (except at the base) closely punctured, the apex
298 Mr. P. Cameron on new
smooth and bare; the base of the mandibles covered with
golden pubescence; the palpi are covered with a pale pile.
Pro- and mesothorax thickly covered with bright golden
depressed pubescence; the median segment with pale
fulvous hair. The basal portion of the median segment
is closely transversely striated; the transverse striz are
irregularly intersected by longitudinal ones; on the basal
half in the centre is a longitudinal one ; the apex has an
oblique slope, is irregularly transversely striated, in the
middle is a deep furrow. Propleurz shagreened, covered
with pale fulvous pubescence ; the mesopleure closely punc-
tured and thickly covered with rufo-fulvous pubescence,
intermixed with long pale fuscous hair, as are also the
metapleurz and the mesosternum. The mesosternal furrow
is narrow and shallow ; the transverse furrow at the middle
coxee is deeper and wider; the metasternal process is nar-
rowly, but distinctly, furrowed down the middle; the apex
is divided into two somewhat triangular processes. Legs
densely covered with a golden pile; the hinder tibie are
distinctly keeled in the middle behind ; the calcaria black ;
the tibial and tarsal spines bright rufous. Wings yel-
lowish hyaline, the apex slightly infuscated ; the nervures
and stigma yellow; the first cubital cellule at the top is
hardly one third of the length of the second; the first
transverse cubital nervure is broadly curved; the two
recurrent nervures are united near the top, shortly appen-
diculated, and are received near the apex of the basal third.
The basal three abdominal segments are covered with
depressed golden pubescence; the pygidial area black,
sparsely covered with golden hair; the hypopygium is
closely and distinctly, the penultimate segment sparsely,
punctured. The lateral folds on the mner orbits are promi-
nent; the sculpture of the front and vertex is hid by the
dense pubescence ; the frontal furrow appears to be wide
and shallow.
Allied to 7. Saundersi and T. Rothneyi, but is quite
distinct.
Tachytes fulvo-vestita, sp. n.
Long. 15 mm.
Scape of antennz (except above) thickly covered with pale
fulvous pubescence and more sparsely with pale fulvous
hairs; the flagellum with a pale down. Vertex alutaceous,
sparsely covered with long fuscous hair; the front, face,
and clypeus thickly with long golden pubescence; the apex
Hymenoptera from Northern India. 299
of the clypeus almost bare, sparsely punctured. Mandibles
black, broadly rufous in the middle and above to near the
base; the latter is thickly covered with golden pubescence ;
palpi rufo-testaceous; the basal joimt black at the base.
The eyes at the top are separated by the length of the third
antennal joint; the ocellus is round, not dilated before or
behind. Thorax thickly covered with long bright hair,
which is thickest on the mesonotum. The metasternal area
is flat at the base and narrowly keeled in the middle; the
apex has the sides raised, the raised part becoming higher
towards the apex, which has a slightly oblique slope; the
middle is narrow and deep at the bottom. Legs rufo-
testaceous; the cox, trochanters, and base of femora are
black, which is broadest on the anterior, narrowest on the
posterior pair; the spines are few, stout, and rufous; there
are none on the metatarsus. Wings yellowish hyaline, the
apex fuscous; the first cubital cellule above is about one
fourth longer than the second ; the second recurrent nervure
is received shortly, but distinctly, beyond the middle; the
second is received the length of the top of the second
cubital cellule from the base, the space between the two
is a little greater than the length of the first cubital cellule
above. Abdomen shining; the petiole covered with long
pale hairs, the pygidium with stiff rufous hairs.
Comes near to 7. fulvopilosa; may be known from it by
the hinder tibiz not being so stout, by the metatarsus being
more slender and without spines, by the eyes at the top not
being so widely separated, and by the different form of the
metasternal area.
Tachytes maculipennis, sp. n.
Nigra, femoribus late, tibiis tarsisque rufo-testaceis; capite
thoraceque pallide fulvo-pilosis; alis hyalinis, fusco macu-
latisn Ge
Long. 12-13 mm.
Antenne black, the scape broadly testaceous below; the
‘scape beneath thickly covered with pale fulvous hair;
the flagellum with a pale down; the front, face, and clypeus
thickly covered with golden pubescence; the ocellar region
and vertex alutaceous, covered with long pale fulvous hair;
the hinder ocelli are more distinct than usual and are placed
near each other; there is a narrow furrow in the middle of
the vertex. The basal third of the mandibles pallid yellow ;
the middle rufous, the apex black ; the base is covered with
pale golden pubescence; the palpi rufo-testaceous. The
300 Mr. P. Cameron on new
thorax is thickly covered with golden pubescence and with
long pale fulvous hair. The pronotum is deeply and dis-
tinctly separated from the mesonotum, which is closely
punctured. The hair on the postscutellum and the median
segment is long and thick; on the apex of the basal region
of the latter is a small, smooth, triangular space. The pro-
pleure are rather bare; in the middle is a curved, smooth
and shining, narrow furrow. The pubescence on the meso-
and metapleurz is dense; the hair is long and paler. Legs
rufous; the coxe, trochanters, the four anterior femora
broadly behind to near the apex, and the hinder at the base
above and more broadly below, black; the front femora
behind are covered with golden, the posterior four with
pale, pubescence. Wings hyaline; along the nervures suf-
fused with fulvous clouds; the lower third of the first
transverse cubital nervure is straight, the upper part is
oblique ; the first recurrent nervure is received nearly the
length of the second cubital cellule from the base of the
cellule, the second shortly beyond the middle. Abdomen
shining, smooth; the segments banded with silvery pubes-
cence; the pygidium is densely covered with silvery
pubescence ; the hypopygium is roundly and deeply incised
on the apex.
Liris violaceipennis, sp. n.
Niger, dense argenteo pilosus ; alis fusco-violaceis. 2.
Long. 13 mm.
The middle of the scape brownish beneath, thickly covered
with silvery pubescence; the flagellum with a pale pile.
Front and vertex alutaceous, opaque; the ocellus has a
triangular process in front; behind the ocellar region is
a deep triangular depression ; there is a longitudinal shallow
furrow behind the ocellus. ‘The cheeks and clypeus are
thickly covered with silvery pubescence; palpi thickly
covered with white pubescence. Pro- and mesonotum
thickly covered with a pale down; on the centre the down
has a fulvous tint. Median segment opaque, alutaceous ;.
the apical slope has a narrow shallow furrow in the middle ;
the sides are obscurely transversely striated. Metapleurze
obscurely irregularly striated. Sternal process large, dis-
tinctly keeled down the middle ; its apical lobes rounded.
Wings with a distinct violaceous tint; the second cubital
cellule at the top is nearly four times longer than the first ;
the upper half of the first transverse cubital nervure has,
above the middle, a different slope from the lower half; the
LIymenoptera from Northern India. 301
second recurrent nervure is received near the apex of the
basal third of the cellule; the two recurrent nervures are
separated by the length of the top of the first cubital cellule
from each other. Legs pruinose; the spines and calcaria
black. Abdomen with the segments banded with silvery
pubescence; the pile on the pygidium is dark golden in
certain lights; the hypopygium is slightly triangularly
depressed at the apex.
Comes near to L. nigripennis, Cam.; that may be known
from it by the head and thorax having a golden pile, by the
pile on the pygidium being golden, by the apex of the
median segment being more cl8sely and uniformly trans-
versely striated, by the femora having golden hair, and
it is altogether a larger and stouter insect.
Tachysphex tinctipennis, sp. n.
Niger, capite thoraceque dense albo pilosis; alis hyalinis, cellula
cubitali 1* duplo longiore quam 2". 2.
Long. fere 10 mm.
Scape of antenne shining, densely covered with silvery
pubescence, the flagellum with a pale pile; the pedicle
densely pilose. Front and vertex closely punctured, the
vertex less closely behind the ocelli, the front densely
covered with white pubescence, the ocellar region raised, a
shallow furrow down the middle; the depression behind
them is deep in the middle. The apex of the clypeus is
shining, bare, shghtly wrinkled. The mandibles behind
the tooth are finely rugose, pilose; palpi dark testaceous.
Mesonotum densely punctured and thickly covered with
fuscous pubescence. Scutellum shining, less closely punc-
tured ; postscutellum finely rugose. The basal part of the
median segment is irregularly longitudinally striated, the
apical closely finely reticulated ; the apex has an almost
perpendicular slope and is transversely striated. Propleurz
shining; mesopleure closely and distinctly punctured, the
tubercles behind thickly banded with silvery pubescence,
the perpendicular furrow is crenulated; the metapleure
closely, slightly obliquely, striated. Mesosternum closely
punctured, thickly covered with white pubescence; the
metasternal process is depressed at the base, raised at the
apex; there is a stout keel in the middle at the base.
The first cubital cellule is double the length of the second
on the top, the first transverse cubital nervure has an
oblique slope near the middle; the second recurrent ner-
vure is received shortly behind the middle. Legs thickly
302 On new [ymenoptera from Northern India.
covered with a silvery pile; the tibial and tarsal spines are
silvery white. Abdominal segments with silvery bands;
the pygidium bare, shining, and bearing a few scattered
punctures.
This species comes close to 7. bengalensis; it has not
the wings clear hyaline, they having a distinct fuscous
tinge. In 7. bengalensis the second recurrent nervure is
received distinctly beyond the middle, in the present species
distinctly behind it ; the median segment is not so distinctly
reticulated ; the basal half is more distinctly longitudinally
striated ; and it is a smaller and more slenderly built
species. .
Larra apicepennis, sp. n.
Nigra, mandibulis late rufis, basi metanoti reticulata, apice striolato ;
alis hyalinis, apice fumatis. @.
Long. 7 mm.
Head above the antenne coarsely aciculated, the furrow
below the single ocellus deep; the clypeus shining at the
apex, semicircularly depressed above and closely punc-
tured ; pro- and mesothorax closely punctured; scutellum
more shining and with the punctures more widely separated.
The basal part of the metanotum is closely and finely
reticulated, the reticulations becoming finer and closer
towards the apex; the apex has an oblique slope and is
finely and closely transversely striated, the striz being much
stronger on the apical half; the middle furrow is deep.
Legs black, pruinose, the tibiz and tarsi strongly spined.
Wings hyaline and iridescent to the base of the stigma, the
rest slightly, but distinctly, smoky; the apical abscissa of
the radius is oblique and is as long as the top of the first
cubital cellule, which is above nearly twice the length of
the second; the upper and middle parts of the third trans-
verse cubital nervure have oblique slopes, the lower part
is roundly curved. Abdomen pruinose, shining ; the basal
third of the pygidial area is smooth, bare, and shining, the
rest is closely punctured and covered with a rufous pile;
the hypopygium is strongly, but not very closely, punctured.
The metapleurz are obscurely obliquely striated.
The wings have a steel-blue reflection in certain lights.
Apidae.
Halictus carinifrons, sp. n.
Black, the flagellum of the antennz brownish beneath ;
On an undescribed Genus of Coreide. 303
the hair is white, on the underside of the tarsi fulvous; the
wings hyaline, the nervures and stigma black. ?.
Long. 6-7 mm.
Head smooth and shining, sparsely haired, the mouth
fringed with longish rufous hair; there is a distinct longi-
tudinal keel on the lower half of the front. Mandibles
piceous towards the apex. ‘The area on the median segment
is closely irregularly reticulated ; at the sides it bears some
longitudinal keels ; its apical slope is straight and slightly
oblique ; on the apical half is a large, somewhat oval, deep
fovea; its sides and top are keeled, but not strongly. The
spines on the calcaria are as iong as the thickness of the
spur; they extend to near the apex and become gradually
shorter from the base to the apex. Abdomen smooth and
impunctate, above it is almost bare; below the hair-fringes
on the basal five segments are broad, long, and white; the
apices of the segments are brownish, the anal fimbria is
distinct, rounded behind, and rufous in colour. The labrum
is entire, rounded, and slightly narrowed towards the apex.
The pleural tubercle is broadly fringed behind with white
hair.
XXXVI.—An undescribed Genus of Coreide from Borneo.
By W. L. Distant.
HETEROPTERA.
Fam. Coreide.
Subfam. Corzrm.
Division MICTARIA.
KENNETUS, gen. nov.
3. Body elongate, somewhat slender; head longer than
broad, cleft between the apices of the lateral lobes, eyey well
separated from the anterior margin of the pronotum; antenne
long, first joint a little shorter than fourth and about as long as
anterior femora, second and third joints shortest, second a little
longer than third ; rostrum reaching anterior coxe, first joint
extending to base of head; pronotum with lateral angles very
longly produced in elongate processes which are a little
convex above and concave beneath, directed moderately
804 On an undescribed Genus of Coreide.
upward and forward, but their apices barely attaining to the
latitude of the head, their anterior and posterior margins
‘serrate, the latter more strongly so, their apices broad and
medially angulate, lateral pronotal margins in front of pro-
cesses and lateral abdominal margins finely serrate; scutellum
of moderate size, subtriangular ; membrane as long as lateral
margin of corium, veins strong and obliquely longitudinal ;
second abdominal segment with a tuberculous spine on each
side near its posterior margin; anterior and intermediate
femora moderately thickened, toothed beneath near apex,
posterior femora incrassate, moderately curved, strongly
spinous on their under surface, the strongest spine being near
apex, and with about three strong curved spines on their
upper surface ; trochanters with an apical spine ; anterior and
intermediate tibia slender, moderately thickened at apices, and
longitudinally furrowed; posterior tibize dilated on each side,
the inner margin toothed beyond middle, the upper margin
with a small upright spine at apex ; tarsi with the first joint
robust and about as long as the remaining joints together.
Allied to Prionolomia and Prioptychomia.
Kennetus alces, sp. n.
d. Brownish testaceous, finely pilose, head greyishly
pilose ; sternum with a broad oblique greyish fascia extending
from anterior to posterior coxe; abdomen beneath dark
ochraceous, its lateral margins and apex greyishly pilose ;
apical joint of antenne fuscous; apical areas of produced
pronotal processes, the tibize, and tarsi castaneous; mem-
brane shining cupreous; scutellum with an elongate spot at
each basal angle and the apex ochraceous; pronotum finely
rugulose ; scutellum transversely striate; apices of pronotal
process centrally angulately produced.
g. Long. 31 mm.; exp. pronot. ang]. 23 mm. ; abdomen
at base 8 mm.
Hab. Borneo: Matang (Coll. Dist. and Sarawak Mus.).
This fine Heteropteron was sent to me for identification by
Mr. R. Shelford.
MERCENNUS, nom. n.
Melania, Dist. Proc. Zool. Soc. 1901, i. p. 826 (nom. preocc.).
Type, MW. gracilis, Westw.—Singapore, Java, Borneo.
On Lepidoptera Rhopalocera from Brazil. 305
XXXVII.— The Collections of William John Burchell, D.C.L.,
tn the Hope Department, Oxford University Museum.
IV. On the Lepidoptera Rhopalocera collected by W. J.
Burchell in Brazil, 1825-1830. By Cora B. SANDERS,
of Lady Margaret Hall, Oxford.
[Plate VI.]
In the course of the identification and arrangement of the
large collection of butterflies in the Hope Department the
Burchell specimens fell into their places in the various groups.
Every fragment has been retained, even when the series of
individuals was a very long one, because of the historic
interest which attaches to the carefully preserved data. The
identification and arrangement are the careful work of
Mr. W. Holland, and in cases of special difficulty I have taken
the specimens to London for comparison with those in the
Godman-Salvin Collection and the British Museum. In
making out many of the most puzzling species of that difficult
subfamily the Ithomiine the late Mr. Osbert Salvin, F.R.S.,
very kindly gave me the invaluable help of his intimate
knowledge and long experience. Dr. F. D. Godman, F.R.S.,
has similarly come to my aid with the most difficult of the
Satyrine, and has also promised to name the whole of the
Burchell specimens in the group upon which he is so distin-
guished an authority—the Hesperiidae. Kind help has also
been afforded by Mr. F. A. Heron, of the British Museum.
When the arrangement of the Rhopalocera was sufficiently
advanced I suggested to Miss Sanders that it would be of much
interest to prepare an account of the Burchell specimens, incor-
porating all the dataand observationsrecorded on the specimens
and in the note-books. As I have explained above, Miss
Sanders is not responsible for the identification of the species,
although she has taken specimens to London to compare them
afresh when it appeared possible that there might be some
slight difference between them and the individuals captured
in more recent years. For such possible differences Miss
Sanders has kept the keenest outlook, aided in the search by
Mr. Holland and myself; and it will be seen that the quest
has not been altogether fruitless. The explanation of any
recognizable differences, as due to a genuine change of form
in three quarters of a century or to alteration in the distribu-
tion of forms, will be considered in each case as it arises. It
may be said, however, that the evidence of some change is
Ann. & Mag. N. Hist. Ser. 7. Vol, xiii. 20
306 Miss Cora B. Sanders on the Rhopalocera
greater than we ventured to hope for at the outset of the
enquiry.
I have claimed that the Burchell Collection, with its
numberless accurate data, is of the highest historic importance
in enabling us to carry back “ the detailed record of the occur-
rence of many thousands of species in two most interesting
parts of the world, and to construct a trustworthy standard by
which to measure the rate of future change” (Ann. & Mag.
Nat. Hist., Jan. 1904, p. 46). The trustworthiness of the
standard depends upon the persistence of the data unaltered
from Burchell’s time to this. There is, fortunately, the means
of checking these data by comparison with a list of the Brazilian
Arthropoda made under Professor Westwood’s direction
during the years which immediately followed the gift of the
collection in 1866. A second list of the dates of every indi-
vidual of a species in Professor Westwood’s handwriting is
found on one specimen of many species, and this has often
been a valuable check upon the complete list when errors
were suspected.
The first section of the butterflies is written in Professor
Westwood’s own handwriting, and deals with the Heliconiide
in the old broad sense, comprising the Ithomiine, the genera
Lycorea and Ituna of the Danaine, and the Heliconiine.
Although in the form of rough notes and very difficult to
disentangle, it is a model of accuracy. It records the whole
of Burchell’s notes written on the labels accompanying the
specimens, but apparently none of the facts to be found in
his manuscript note-books. Beyond the Heliconiide the list
of butterflies is continued in an extremely clear handwriting,
with great neatness of arrangement, but containing occasional
slips and mistakes which can be detected by careful comparison
with the existing data. I1is evident that Professor Westwood
arranged the vast mass of material into groups and sub-
groups, and in each of these separated the forms into what he
believed were distinct species. An assistant employed under
his direction then copied the notes written by Burchell on the
labels attached to each specimen. In some cases Westwood
himself added names to the forms thus grouped together in
the list ; but in the vast majority of cases the list remains
as it was written by his assistant. My inference from the
handwriting has been kindly confirmed by my friend Miss
Swann, who tells me that her uncle, Professor Westwood,
employed an assistant to write for him about the time at
which these lists were copied. The backs of old University
Notices were employed for this purpose, and a rather valuable
record of the acts of the University during some of the years
collected by W. J. Burchell in Brazil. 307
before the appearance of the ‘Gazette’ is to be found on the
reverse sides of the sheets!
A few Notices of the years 1864, 1865, and 1867 are thus
employed, together with large numbers issued in 1866 and
1869. A single paper with the date 1871 is made use of.
It is therefore almost certain that the list was begun at once
and finished within about six years of the gift. My first
experience of the Department was in the summer of 1873,
and I feel sure that the work was not going on then and was
not resumed at a laterdate, Professor Westwood was keenly
interested in the collection and appreciated it at its true
worth. About six months after its arrival in Oxford he had
already made a preliminary survey, and, on Noy. 26th, 1866,
gave an account of it to the Ashmolean Society. The
‘Proceedings’ of this Society are very rare, and I have
thought it well to reprint the passages in which the collection
is described and its great significance demonstrated.
“On the Data afforded by the Burchellian Collection as to
the Geographical and Modificational Ranges of certain
Brazilian Insects. By J.O. WEstwoop, M.A., F.LS.,
Hope Professor of Zoology.
[‘ Proceedings of the Ashmolean Society,’ New Series, No. I.
Read Monday, Noy. 26th, 1866. ]
“Professor Westwood gave an account of the very exten-
sive collections in various branches of zoology formed in
South Africa and Brazil by the late Dr. W. J. Burchell, and
presented to the University of Oxford by his surviving sister,
in recognition of the honour conferred on her brother by the
degree of D.C.L. some years previously. The collection was
extremely rich, both in the number of species and also of
individuals, and was especially valuable from the great care
which had been taken in attaching the date of capture to every
specimen, whereby, in conjunction with the journal kept by
Dr. Burchell, the amount of geographical range and modifica-
tional change of each species could be accurately determined.
The Brazilian portion of the collection had been made during
a visit extending over three years [in reality nearly five
years], in which period Dr. Burchell investigated the natural
history of Rio Janeiro and its neighbourhood, thence pro-
ceeding southwards to Santos and San Paulo, thence north-
westwards to Goyaz, and thence due north by the Tocantins
to Para and its neighbourhood. Copious note-books were
kept, and entries made daily, so that it may safely be affirmed
that in respect to its geographical data no collection equal to
this has ever reached Kurope. The donation of the collection
20*
308 Miss Cora B. Sanders on the Rhopalocera
to the University was also very opportune at the present
moment, when the question of the existence of species, and
the extent of variation to which they are subject, are especially
attracting the attention of zoologists.”
After giving an account of the views of various writers on
these questions and expressing his own belief “in the inde-
pendent and original creation of species,” Professor Westwood
concluded as follows :—
“ A careful study of the Burchellian collection required to
be made, and it could not be doubted that it would afford
satisfactory data for ascertaining the specific status of many
of the insects which had fallen under Dr. Burchell’s notice.”
Tt is a keen pleasure to me to realize that in gradually
publishing an account of the Burchell Collection I am carrying
on a work to which my great predecessor devoted so much
time and thought.
A search through Burchell’s manuscript brought to light a
scrap of paper covered with figures which tell us much of the
man and his work. It is a memorandum of the dates at
which he unpacked each section of his immense collection of
insects and relaxed and set out the specimens. The majority
of the dates refer to the “ Lepidoptera &c.,”’ and these are
reproduced below :—
“ Lepidoptera &c. relaxed and put out.
[Specimens captured between Relaxed and set out
following dates. | [between following dates].
7. 9.28 to 28. 2.29 [Set] 26.12.39 to 8.1.40
28. Jeno ass 296 4.129 5 10, AAO” ay irre ee
SON oo tans 5.2.80 5, 4. 2.40 ro eee
Lepidoptera &c. relaxed and put out from the Cedarwood Box
containing [captures] from 20. 7. 27 to 16. 4. 28.
25. 8.27 toa[m.]29. 8.27 “[Set] 12. 2. 44 _——
68 Ot es 26. 8. 27 is 6. 4.46 to 30. 4. 46
3 2.126) ais 14. 2.26 9) BO) 4746, 220) 646
21. A. 26. s; 9. 2. 26 9, 22s B. 46 —,, 022, Joa
Lepidoptera of Rio de Janeiro, Minas, &c., &c.
27. 1.26 co 8. 2.26 [Set] 24. 7.46 to 28. 7.46
—_—- ,, 7 fee ee 45) sf 2G tO oy eel. ee
14, 126.2 - aj WhOdics TaeG hee - ais
ol, 12.95.05) 146 . it. (87 AG™ AaB ete
6242525 23) 31. 12. 25 i. 6. 8:46 -.,, 10.846
78s QO 6. 12. 25 59.) DA 846. i oA er
At. 2504, 6. 11. 25 oy dO. B46 po ORS eaG
eA S26 vies 6. 12. 25 9. 20. 08.46 . ghee
29.10.'25 — ,, 4.11. 25 3. 2k 88; 46 See ee as
999]27. 10.25 ,, 29.10.25 ,, 22, 8.46 4 8.9.46
819]23.10.25 ,, 998]27.10.9 , 8 9.46 ,, 23.9. 46
N.B.—Finished putting out and unpacking the whole of my Brazilian
Insects on 26. 9. 46.”
collected by W. J. Burchell in Brazil. 309
This mechanical labour was therefore completed when
Burchell was about 63 years of age, 1634 years after the
Brazilian journey came to an end in February 1830.
It is hardly necessary to add that the specimens were set
in our old insular style, sloping and low upon the pin.
Nearly all the butterflies have now been reset in accordance
with modern requirements.
Burchell’s method of keeping his notes on the Arthropoda
was changed as time went on. At first he sorted out the
captures of each day into what he believed to be species, and
gave a list of these, and, in another column, the number of
individuals belonging to each. Opposite these numbers
observations of habits were sometimes recorded. During his
journey to Rio, between April 2 and July 6, 1825, he had
captured 97 kinds, distinguished by the numbers 7-97 (in
Portugal, at Madeira, at ‘Teneriffe, and on the ship). Be-
tween July 26 and Oct. 27, 1825, he had similarly distin-
guished species 98-7022 (during the earlier months of his
residence at Rio and the greater part of his excursion into
Minas Geraes). The labour was probably excessive and in
the majority of cases served no specially valuable purpose ;
for the same work could be done better after his return home.
Accordingly we find that he employed this method for the
Jast time on Oct. 27, 1825, explaining a new meaning for all
the numbers beyond 7022 in these words:—‘ N.B. The
following Numbers are of such Insects on/y as require special
and particular remark: of all the others their locality and
season can be known only by referring to that same date in
the Journal, or in the Catalogus Geographicus of the Botanical
Collection: or to the following list of dates.” ‘The Journal
is unfortunately lost, but the other two books are in the Hope
Department, the second (‘‘ the following list of dates’) being
what I have called the “ Brazilian note-book.” In this
latter the numbers 7023 to 1345 (Jan. 1, 1826, to March 18,
1829) occur among other entries which are distinguished by
dates alone, and not by numbers. All the numbers beyond
1022 and some of the dates refer to observations made upon
the living forms. ‘lhe numbers of individuals are not given,
but can sometimes be inferred from the descriptions. The
last number 7345 refers to an observation made at Porto
Real (Nacionale) on March 18th, 1829; so that all the
observations made during the descent of the Tocantins and at
Paid, in fact from March 19, 1829, to Feb. 10, 1830, are lost,
having been contained in the missing volume alluded to on
p. 93 (Ann. & Mag. Nat. Hist., Feb. 1904).
lt is much to be hoped that an opportunity may be found
for publishing the two Oxford note-books, both on account of
310 Miss Cora B. Sanders on the Rhopalocera
their high intrinsic interest and because of the irreparable
injury which their loss or destruction would inflict upon this
historic collection. In order to render this and the following
papers of greater permanent value, and to bring them into
relation with such a publication whenever it may be issued,
I propose to reproduce any of Burchell’s reference numbers
which are still to be found attached to the specimens. The
vast majority of these are, however, distinguished by their
dates, and have no such numbers. The following example
will serve clearly to distinguish between Burchell’s reference
numbers and those which are now added to bring the speci-
mens into relation with these papers :—
Be. 00) alld =) 2a al0, 20s 2 2s ehkeOs
Burchell’s reference number will be printed before the date
of capture and in italics, while the numbers now added will
always appear after the date and printed in heavy type.
Bz. indicates that the date or number immediately following
is an original label, written in Brazil. JJ/. refers to the
number of individuals recorded in Burchell’s note-book as far
as the number 1022. In this case two are accounted for by
specimens 87 and 38, while the third is to be found upon 40
under an allied species. ‘The + indicates that the specimens
also bear labels which were carefully written and added after
Burchell’s return to England. Examples are seen in the
labels to the right of figs. 9 and 10 on Pl. VI., where the
Brazilian number is lowest. When &z. is wanting, Burchell
had copied the reference number and removed the original, as
in the label accompanying fig. 11. #2. without the + is
used when the specimen bears only a Brazilian label (as in
fig. 6). In all such cases as this the dates have been recovered
from the Brazilian note-book. All the other figures on
Plate VI. are without Brazilian labels, and bear dates, some-
times accompanied by notes (figs. 5 and 8), carefully written
after the return home; and this is true of the great majority of
the specimens hereafter recorded, all, indeed, of which the
dates are not preceded by italicized letters or numbers. In
many cases the original Brazilian date was never copied and
remains as the only label. Such dates are preceded by Bz.
I trust that these directions will enable the reader to
ascertain at a glance exactly what records of the great natu-
ralist accompany or refer to each specimen in the collection to
which he devoted so large a part of his life.
kK. B. Pouuron.
Oxford, Jan, 25, 1904,
collected by W. J. Burchell in Brazil, 311
I. Jruomrrmz.
Fleterosais edessa, Hew.
16. 9. 26. 2 § =1,2. Santos. “ Close above the Monastery
of Sio Bento.” “ Ad marginem Sylva.”
23. 9.26. 4 ¢=3-6,1?9=%. Santos. 3and 7 bear Bra-
zilian labels.
26.11.26. g=8. Santos. “In the chdcara (where I
resided) near the Monastery of Sao Bento.”
It has already been stated that the list of Ithomiine is in
Professor Westwood’s handwriting.
The determination and sexing of specimens 1-8 agree with
Westwood’s. His notes show that there were two more
specimens which cannot now be found. Both were males
and dated 12. 1. 26 (Rio) and 23. 9. 26 (Santos).
Hymenitis adasa, Hew.
Bz. 6938. I. 22.10.25. 9 =9. MinasGeraes. “ Ina Roca
(about 4 miles 8.S.W. of the house of Discoberto), on
the road towards San Joao de Nepomucena.” ‘ Pa-
pilio.”
8. 2. 26. 3 9 =10-12. Organ Mountains. Near head of
R. Pacaqué. “In a ride to the Cattle Pounds and the
Milho Roga.”
Agrees with Westwood’s notes except as regards 12,
Concerning this specimen he had written ‘f Very like adasa,
but with difft. veins,” and ‘ Not in Hewitson Coll. or book.”
On 11 he had written in pencil “f 2 agrees with adasa 9 Hew.
in its veins of h. w. but not with ¢.”
Hymenitis erruca, Hew.
D3: 9 2G6e 29S. 0138, 147 (Santos:
Determined by Westwood as polissena §. On18 he wrote
“seems identical with Polissena from Quito.”
Pseudoscada sp. near utilla, Hew.
8.2.26. g=15. Organ Mountains. (As 10-12.)
Compared with Hewitson’s specimens of utdl/la in the
British Museum 15 appears to be a less heavily marked
form of the same species.
Determined by Westwood as ¢ acilla.
312 Miss Cora B. Sanders on the Rhopalocera
Pseudoscada Jessica, Hew.
11. 2. 26. 2 6 = 16,47... Organ . Mountains. ““By “the
River Pacaqué.” ‘In a walk to the Ipé trees.”
14, 2.26. g=18. Organ Mountains. Near R. Pacaqué.
Agrees in all respects with Westwood’s notes. Burchell’s
manuscript label was missing from 18, ‘The date was re-
covered from Westwood’s list.
Pseudoscada acilla, Uew.
4.11.25. ¢@=19. Minas Geraes. Francisco Manoel’s
Rancho. Near NepOmucéna.
8. 2.26. g=20. Organ Mountains. (As 10-12.)
9.2.26. d= 21. + “ By the River Pa-
caqué.”’
Agrees in all respects with Westwood, except that 15 was
also included under acilla.
Ithomia agnosia, Hew.
10. 11. 25. 3 @ = 22-24, Minas Geraes.
‘These three specimens were carefully compared with twenty-
three in the Hope Department, one in the British Museum, and
a series in the Godman-Salvin Collection, none, however, being
from Brazil. A very few examples (one from Colombia) in
the Godman-Salvin Collection occur approaching the Burchell
form. The Burchell specimens vary from the usual form in
having no extension of the black diagonal band on the fore
wing into the interspace between the second and third median
nervules, and a narrower marginal band on the hind wing.
The general effect of the difference between these in the
specimens mentioned above is that the transparent part of the
wings is much more prominent in the Burchell examples.
In fact the difference resembles that between phenomoe and
Burchelli (compare figs. 3 and 4 with 1 and 2 on Pl. VIL),
described on p. 315. In both cases South-Hast Brazil is
characterized by a form in which the transparent area of the
wings is increased at the expense of the black markings.
Agrees with Westwood’s notes. He had written the words
** agnosia, Vvar.,” on 22.
Ithomia phono, Hiibn.
No data. 2? = 25.
Bz. 196. 1. 8.9.25. 2 = 26. Rio Janeiro (along the Aque-
duct). ‘* Papilio (Heliconius) In Sylva.”
collected by W. J. Burchell in Brazil. 313
852. 0.4 24.10.25. 9 =27. MinasGeraes. “ About Joao
Pedro’s at Discoberto: at the margin of the forest.”
“Papilio.”
10. 1.26. 9 =28. Rio de Janeiro, Praia Grande, and
vicinity.
14. 1. 26. 9 =29. Rio de Janeiro. Valley of Laran-
jeiros and about Sao Jofio de Carahy at Laranjeiros.
11. 2. 26. 2 ¢=80, 31. Organ Mountains. (As 16, 17.)
Bz. 18.3. 26. 2 ¢ = 82, 38. Rio de Janeiro. Along the
Carioca Aqueduct.
£6. 922602'¢ = 34; 35. Santos. (As. 1, 2:) Brazilian
label on 34.
Agrees in all respects with Westwood, save that as regards
either 32 or 33 he had written “1 ¢ with v[ein] of H. W.
abnormal.”’
Pteronymia hemixanthe, Feld.
Bz.335. 1. 15.10. 25. ? = 36. Minas Geraes. “ Fap[ilio}.
At the Discobérto do Antonio Velho. In floribus Lia-
tridez albiflora.”
907. UL+ 25.10.25. 2 9 = 87, 38. Minas Geraes.
“ Pfapiliv]. At Discoberto, near Joao Pedro’s house.”
Specimens not sexed by Westwood. His determination
agrees.
Pteronymia euritea, Cram.
Bz.317.I. 14.10.25. ¢=39. Minas Geraes. Discoberto.
“Horta.”
Bz. 907. H10.+ 25.10.25. 9 =40. Minas Geraes. (As
37, 38.)
S11, 95, 6 —41,,. Minas Geraes.” ““Sylvatiea.”
8. 2. 26. 2 6 = 42, 48. Organ Mountains. (As 10-12.)
Oe DOs 2 CG = 44. 4s 45 ‘ (As 21.)
Pe 226-92 VS = AG, 4h, 3 (As 16, 17.)
a 2. 26. O48} “s ne (As 18.)
22 26: 6 = 49: Near the R. Pa-
9? 9?
caqué, “ along the road by the Rancho for 1} mile from
the house.”
18. 3. 26. 2 ¢=50, 51. Riode Janeiro. (As 82, 33.)
Bz. 26.11.26. 9 =52. Santos. (As 8.)
[The fact that the two closely similar species, hemixanthe
and euritea, are to be found flying together 1s of much interest.
Their remarkable resemblance in the fresh state is well shown
by the inability of this acute observer to discriminate between
them. ‘Thus no. 907 was found upon two specimens of the
314 Miss Cora B. Sanders on the Rhopalocera
first-named species (37 and 38) and upon one of the last-
named (40). But the group also includes another less nearly
related species which Burchell failed to separate. The
number 335 is found upon P. hemixanthe (86) and ITetero-
scada yanetta (180), indicating that they were taken for the
same species on the same day visiting the same flowers,
accompanied by Pteronymia sao (53) and Dircenna dero (67,
68), both of which were recognized as distinct. Furthermore,
in the note-book we find the numbers ‘335... (377),” indi-
cating a second time that the latter, P. eurttea (39), was
considered to be the same as hemizanthe, and, in this case, the
same as [7. yanetta also.
Burchell was able to penetrate the disguise of other ex-
amples of mimicry, such as the resemblance of certain Hemi-
ptera for the Hymenoptera; but in the remarkable synapo-
sematic likeness between the nearly allied species of Ithomiine
there was nothing to arrest his attention—E. B. P.] |
Specimens not sexed by Westwood. His determination
agrees. He gives the dates of six additional specimens of
euritea Which cannot now be found. One of these bore the
same date as 42, 48, two the same as 44, 45, one the same as
48. One was dated 4. 11. 25 (Minas Geraes, near Nepo-
mucena, Francisco Manoel’s. ‘he notes show that the
specimen might have been captured by “ some tropeiros from
the rancho”). One was dated 31. 12. 25 (Rio; on the
Corcovado Mountain, and in the Valley of Laranjéiros).
Pteronymia sao, Hiibn.
Bz. 338, 1.15.10. 25. «2 = 538. .Minas'Geraes, © Fapieleoy
cum 335.” (As 86. The whole note applies to 53.)
Agrees in all respects with Westwood’s notes.
Fteronymia nr. artena, Hew.
8. 2.26. 9? =54. Organ Mountains. (As 10-12.)
14. 2. 26. g = 56. 3 r (As 18.)
Compared with Hewitson’s type of artena in the British
Museum, 54 and 55 appear to be a less heavily marked form
of the same species.
On 55 Westwocd had written “artena but with only a
minute white stigma instead of a larger 4-patch,” and as
regards 54 a difference in venation is alluded to and explained
by reference to a rough diagram, ‘The sexing agrees,
Pteronymia sylvo, Hiibn.
12. 11,25. g¢ = 56. Minas Geraes. ‘ At Mandioca.”
collected by W. J. Burchell in Brazil. 315
10. 3. 26. 9? =57. Rio de Janeiro.
20d. 2055 i= DOernd 55 © * Along the Carioca
Aqueduct.”
Specimens not sexed by Westwood. His determination
agrees,
Leucothyris nr. makrena,
4.11.25. ¢ =59. Minas Geraes. (As 19.)
Westwood had written ‘‘ Makrena var. absq[ue] fascia in
cellula al. ant.,” but the fascia here alluded to appears to vary
considerably. The sexing agrees.
Leucothyris phenomoe, Dbl. & Hew.
11. 2. 26. ¢=60 (PI. VI. fig. 3). Organ Mountains. (As
16, 17
6, 17.)
14, a 26. ¢ = 61 (Pl. VI. fig. 4). Organ Mountains. (As
8.)
Bz. 19.3. 26. §=62. Rio de Jan. “In the Valley of
Catombi.”
23. 9. 26. ¢ = 63. Santos.
Burchell’s labels, written in England, are reproduced to
the right of the figures to which they respectively refer.
Specimens not sexed by Westwood, except 61 ¢. His
determination agrees.
Leucothyris phenomoe, Dbl & Hew., n. subsp. Burchell.
(PL VI. figs. 1.& 2:)
19. 5, 29. 2 ¢ = 64 (Pl. VI. fig. 1), 65 (Pl. VI. fig. 2).
Descent of the Rio Tocantins, between S. Antonio and
Itaboca. Araguay.
Burchell’s tabels, written in England, are reproduced to
the right of the figures to which they respectively refer.
[The form Burchell is at once distinguished from typical
phenomoe by the greater development of the black markings
in general, giving the insect an entirely different aspect,
which will be appreciated when figures 1 and 2 on PI. V1,
are compared with 3and 4, ‘The black borders of both wings,
including the inner margin of the fore wing, are broader in
Burchelli, as is the black band which obliquely crosses the
middle of the cell in the fore wing. But the chief difference
is seen in the principal marking, which descends obliquely
from the costa of the fore wing across the apical boundary of -
the cell. This broad black band is, in Burchell, prolonged
beyond the cell in the interspace between the second and third
median nervules so far that its total length is about.50 per
316 Miss Cora B. Sanders on the Rhopalocera
cent. greater than in phenomoe. Furthermore, in the former,
but not in the latter, the band is continued in a much
narrower form along the second median nervule until it joins
the black hind marginal border near the anal angle of the
wing. The development of thisimportant marking gives it a
different shape, the proximal border being markedly concave
in phenomoe, straight or slightly convex in Burchelli, the
concavity of the distal border being more pronounced in
Burchelli.
The type of Burchell’, specimen 64 from the junction of
the Rio Araguay with the Rio Tocantins, is represented in
Pl Vie ties:
Distribution (based on the specimens in the Godman-Salvin
Collection and the Hope Department).—Burchelli occurs in
the northern part of Eastern Brazil, phenomoe in the southern
part, in Argentina, and Venezuela.—E. B. P.]
On specimen no. 65 there is a scrap of paper on which
Professor Westwood had written in pencil “ Like phenomoe,
but larger black band. [? is it a] black var.” There is un-
certainty as to the correct interpretation of the letters enclosed
in square brackets. On 68 he had written a list of the dates
of specimens 60-65, and opposite 19. 5. 29 are the words
“2 ina’. fascia longiori.”” In his list of Heliconiidz the words
are ‘2 ind. fascia ad apicem cellule magis elongata.” There
is also a statement that he submitted a specimen to Hewitson,
who probably suggested the name “ flora black var.,” which
has been added in pencil. These butterflies were carefully
compared with others in the Hope Department and the
Godman-Salvin Collection, and it was found that this heavy
type of marking is probably characteristic of a large section
of the northern part of Eastern Brazil, for two similar forms
captured by the late T. Belt in Maranhao exist at Oxford,
while the Godiman-Salvin Collection contains one similar
form from Pernambuco and one from Bahia. ‘The latter
collection also contains eight specimens from Argentina, one
from Rio, and a series from Venezuela. All these, together
with the Burchell specimens from South-East Brazil (nos. 60-
63) and two Miers specimens (probably Rio) at Oxford, are of
the ordinary form, with lighter markings, as also are six
specimens in the British Museum, which, however, are without
localities.
Dircenna hulda, Feld.
31.1. 26. 9 = 66. Rio de Janeiro. “ Valley of Catombf
anda high mountain on the N.W. side of the Aqueduct.”
collected by W. J, Burchell in Brazil. 317
“All of this date were from off plants, mostly up the
Valley of Catumbi.”
The specimen was named by Westwood epidero.
Dircenna dero, Hiibn.
Bz. 340. II. 15.10.25. 2 9 = 67, 68 (PI. VI. fig. 6). Mi-
nasGeraes. “ P[apilio] cum 335.” (As 36, and taken
with it in floribus Liatridez albifloree.’’)
Bz. 475. IT. 16.10.25. 2 9 = 69,70. Minas Geraes. Dis-
coberto. ‘* Papilio.”
Burchell wrote “475... (340)” in his Brazilian note-book,
indicating his recognition that the four specimens 67-70
belonged to the same species.
Bz. 546.I. 18.10.25. 29 = 71. Minas Geraes. Discoberto.
* Papilio.”
28. 10. 25. 9 = 72 (Pl. VI. fig. 7). Minas Geraes. “ In
the Forest on the West and on the East side of S. Jo%io
de Népomucéna.”
29.10. 25. 9 = 73. Minas Geraes. “In the Forest on
the S.E. side of S. Joiio de Népomucéna.”
1.8.27. g= 74 (Pl. VI. tig. 5). Near S. Paulo: on road
between Jundiahy and Capivary. “ Iter faciendo.”
Burchell’s manuscript labels are reproduced to the right of
the three figures on Pl. VI. (5-7) to which they respectively
refer. ‘That accompanying fig. 6 was written in Brazil, the
others in England.
Westwood, in his complete list, mentions two individuals
captured on 28. 10. 25. He also gave a list of captures on a
label attached to 70, and this agrees with the numbers and
dates here recorded. It is therefore probable that the former
is erroneous and that there were not more than eight indi-
viduals. On 68 Westwood had written “This is the only
individual with the veins of H. W. suffused with black.’
The specimen is shown on PI. VI. fig. 6, where the feature
mentioned by Westwood can be clearly seen when comparison
is made with figs. 5 and 7. Westwood does not note the
sexes. He employs the name dero only.
[I have followed H. W. Bates in regarding D. rhoéo, Feld.,
as a form of dero, differing “only in the greater breadth and
irregularity of the dusky black border of the hind wing,
especially in the female, and in the nervures which traverse
the disk of the same wing being of a yellowish colour instead
of black. In the female the discocellulars and the terminal
parts of the median branches are accompanied by dusky
streaks.’ D. dero, on the other hand, “has the hyaline
318 Miss Cora B. Sanders on the Rhopalocera
disks of the wings always clearer and the black borders more
sharply defined than D. rhoéo. J). dero is peculiar to South-
East Brazil, and is not found in the Amazon region, where
the local form D. rhoéo takes its place. I have seen speci-
mens of D. rhoéo also from the neighbourhood of Bogoté,
New Granada. It flies in thinned paris of the forest in
Ygap6, or flooded districts, in the dry season.” (‘T'rans. Linn.
Soc. Lond. vol. xxiii., 1862, pp. 520, 521.)
I have quoted from Bates in full because, if his information
be correct, we have here certain evidence of change in a local
subspecific form within the narrow limits of five-and-twenty
years. All Burchell’s specimens come from South-Hast
Brazil, and only two of them, viz. nos. 67 and ‘74 (PI. VI.
fig. 5), can be regarded as dero. All the rest are examples
of the heavily marked yellowish hind-winged rhoéo (compare
figs.6 and 7 with 5). It would be unwise to build too much
on the conclusion that a change has occurred, especially as
the interval cannot be more than about twenty-five years,
inasmuch as Bates, when he wrote in 1861, was dealing
with experiences which went back many years. But if
his statements that ‘dero is peculiar to South-East Brazil ”’
and that ricéo takes its place to the north be confirmed, we
are compelled to admit that a rapid change has occurred in
the former area and that in 1825 rhoéo was dominant there.
We should be obliged to regard the biological history as
traversing the history laid down by systematics ; for dero,
with the older name, would then be but a very modern local
form of the more ancestral although more recently named
rhoéo. Should further enquiry support Bates’s statement, it
seems probable that synaposematic grouping has directed the
trend of evolution—that resemblance to more heavily
marked transparent Ithomiine associates in the north has
been an advantage which has caused the persistence of the
pronounced black markings of rhoéo, while dero has been
selected as an approach towards less heavily marked members
of Ithomiine groups in the south.
Ithomiine butterflies with a general resemblance to one
another have a marked tendency to fly together, as Bates
points out in this very species (/. c. p. 521). It has already
been found in the case of Leucothyris phenomoe that the
northern part of Eastern Brazil is characterized by a more
heavily marked form (Burchelli) than the southern part (see
p. 215). In many other cases the tendency towards a
reduction of the black markings of transparent and black
Ithomiine in South-Bastern Brazil has been shown in this
memoir. It was apparent in Pseudoscada sp. nr. utilla (15),
collected by W. J. Burchell in Brazil. 319
Ithomia agnosia (22-24), and Pteronymia nr. artena (54, 55).
This reduction of black and increase of transparency occurring
independently in many genera is probably due to selection in
the direction of synaposematic or Millerian resemblance.—
ibe PB: |
Ceratinia eupompe, Hiibn.
29. 10. 25. 9 = 75. Minas Geraes. (As 73.)
4.11.25. g= 76. Minas Geraes. (As 19.)
8. 2.26. g='77. Organ Mountains. (As 10-12.)
9. 2. 26. 39 = 78-80. ,, 3 (As 21.)
Ble 221263,//9 = 81. 5, 5 (As 16, 17.)
12. 2. 26. 2 2 = 82, 83. Organ Mountains. “By the
River Pacaqué.”
No data. 9? = 84,
Westwood’s notes and label agree in including an addi-
tional specimen dated 14. 2. 26 (Organ Mountains). In other
respects his MS. agrees with the data here recorded. The
determination agrees, but sexes are unnoted.
Ceratinia euryanassa, Feld.
Bz. 563.I. 19.10.25. 9 = 85. MinasGeraes. Discoberto.
“‘Pap[ilio].”
10. 11. 25. ¢ = 86. Minas Geraes. Discoberto.
26. 9.26. 5 g@ = 87-91, 4 2? = 92-95 (92 and 95 bear
Brazilian labels). Santos. ‘ Ina walk to Montserrat.”
“These Papiliones very plentiful in the woods”’: this
referring of course to all specimens taken.
Nordata. 9 = 96.
Westwood gives two more individuals captured 26. 9. 26,
and omits the date 10. 11. 25. ‘The latter may be a slip or
may be due to the later transposition of labels. In other
respects and in the determination Westwood’s notes agree,
but sexes are omitted.
Ceratinia deta, Boisd.
Bz. 330.17. 14.10.25. ¢ =9%. Minas Geraes. Disco-
berto. “Papilio (Horta).”
It is probable that this specimen should bear the number
336 and that it was captured with 98 on Oct. 15th. See note
on 108.
Bz. 336. II. 15.10.25. @=98. MinasGeraes. “ Atthe
Discoberto do Antonio Velho. Pap[ilio]. In Sylvis.”
Be.+ 12.11.25. g@= 99. Minas Geraes. *‘ At Mandioca.”
“ Langsdorfi” is written on the Brazilian label.
320 Miss Cora B. Sanders on the Rhopalocera
12. 2.26. g=100. Organ Mountains. (As 82, 83.)
alice? 26. so ele * + (As 49.)
No data. ? = 102.
The numbers and dates agree with Westwood’s notes.
Westwood’s determination was Ithomia melphis, a synonyin
of deta. The sexes were unnoted.
Ceratinia Barit, Bates.
26.5. 29. g¢=108. Rio Tocantins, N. of Itabéca, below
the Falls of Guariba. ‘ Sylva.”
Brit. Mus. ** Ninonda Hew. var. barii.”
Named by Westwood Jthomia ninonia. Sex unnoted.
Mechanitis polymnia, Linn.
30. 10. 25. (Date probably erroneous, and should be 3. 3. 28
or 10. 12.29. See below.) 9% = 104. Minas Geraes.
‘(In the Forest.) On the N.K. side of the arraial of
So Jofio de Népomucéna.” Locality probably erro-
neous, and should be Goyaz or Pard.
5.3.28 @=105. Goyaz. “Caught by the Rio Ver-
melho, near the Carioca Aqueduct, by *C’.” C refers
to Congo, Burchell’s native assistant.
7.6.29. @=106. Rio Tocantins. 8S. of Pard, Sta. Anna.
7.7.29. 9 =107. Pardé. “ Hastward of my house.”
(105 was submitted to the late Mr. Osbert Salvin on Jan. 16,
1896. He considered it to be the ‘‘ Guiana form of Mechanitis
polymnia.” Although without the black hind wing which
is so common in Guiana, the black markings are strongly
developed on the secondaries of all the three female specimens,
resembling many of the individuals from Surinam &c. The
occurrence of such strongly marked forms so far to the south
as Goyaz was a surprise to me. The somewhat faint but
distinct subapical light bar of the fore wing, which is charac-
teristic in Guiana, is evanescent or absent in these specimens.
—kKE. B. P.]
Westwood records two additional specimens, captured
3.3.28 (Goyaz. “Caught in the town by the Rio Vermelho ;
by C[ongo]”) and 10. 12. 29 (Pardé. “ Suburbane *\.° (Om
the other hand, he does not give the date now affixed to 104,
viz. 30. 10. 25. It is probable that a label has been trans-
posed in the manipulation of the specimens, and that 104
should bear the date 3. 3. 28 or 10.12.29. In other respects
and in the determination Westwood’s notes agree with these
records. ‘The sexes were unnoted.
collected by W. J. Burcheil in Brazil. 321°
Mechanitis lysimnia, Fabr.
Bz. 336.17. 15.10.25. 9 =108. MinasGeraes. (As 98.)
[It is probable that this specimen should bear the number
330 and that it was one of the ‘‘ Papilio ( Horta)” captured
on Oct. 14 at Discoberto. Burchell probably accidentally
interchanged its label with that of 97, either originally in
Brazil or later when he set the specimens. The evidence is"
as follows:—The Brazilian note-book shows that two indi-
viduals believed by Burchell to be one form ‘‘ Papilio (Horta),”
captured on Oct. 14, were numbered 330, and that two others
also believed to be one form, taken on Oct. 15 “in Sylvis,”
were numbered 336. Professor Westwood’s list, repeated on
a specimen of each species, agrees with the existing specimens
in showing one 336 on Mechanitis lysimnia (108) and the
other on Ceratinia deta (98). One 330 is on deta (97) and
the other is now missing, but both of Westwood’s lists agree
in recording that it was affixed to a specimen of dysemnia
which cannot now be found. Either Burchell twice paired
deta and lysimnia as the same form on consecutive days or
he accidentally interchanged one 330 with one 336. The
foilowing fact confirms the opinion that he made the latter
mistake and not the former. A few days later, on Oct. 19th,
we find in his note-book the following entry: “563 ... (336),”
indicating his belief that the single specimen denoted by the
first number was the same species as the two individuals -
denoted by the second. Now 563 is Ceratinia euryanassa
(85), a species which closely resembles C. deta, but only
bears a very rough likeness to JZ. lysimnia. It is therefore
probable that 330 was intended for two specimeus of J/. ly-
simnia and 336 for two of C, deta.—kE. B. P.
iors = 10S a? See Minas Geraes.
(As 19.)
10. Ete 26.2 f= 112, Tidy Minas, Geraes:
6.12.25. ¢=114. Riode Janeiro. “ In an excursion to
the Summit of the Corcovado by the road by the Con-
vent ot Sta. Theresa, and along the Aqueduct.”
31.1. 26. 9=115. Riode Janeiro. (As 66.)
9.2.26. 9 = 116. Organ Mountains. (As 21.)
202526. (Pa>hlib) 5; a (As 82, 83.)
L6G 22 2628 99S P18, + °'g, 5 ow Near River. «Pa-
caqué.
Bly 2. 26-09 LID, ex, 3 (As 49.)
26 2. 26.19 = 1205 * On the Rio Macé”
1, 3. 26. 9 =121. ‘ Along the River Magé, upwards to the
Fazénda da Lagéa.” :
Ann, & Mag. N. Hist. Ser. 7. Vol. xiii. 21
322 On Lepidoptera Rhopalocera from Brazil.
7.3.26. ?=122. Riode Janeiro. ‘“ At Catombi.”
-Bz. 9.3.26. g =123. Rio de Janeiro.
10. 3. 26. @=123 a4. Rio de Janeiro.
15.9. 26. = 124, Santos. “ Papilfio]. At edge of the
Forest, at S. Bento Monastery.”
Bz. 14.12.26. ?=125. Cubatio, Lower Slopes of the
Sérra.
16. 12:26. 9 = 126; 'Cubatao. ©“ Middle+ Part *of tite
ascent up the Sérra.”
4,3. 28. 9 = 127. Goyaz. (As 105.)
Westwood’s name and list agree, except that he includes
two more specimens which cannot now be found—one distin-
guished by the number 330, and a second specimen captured
with 116 on 9. 2. 26. Sexes unnoted.
Aeria olena, Weym.
Bz..$7901.,.21..10. 25.. 2.= 128. Minas -Geraessn “in ta
rossa at Discoberto, and along a channel (on the margin
of the Forest) which conducts water to the house.”
“Pap{ilio].” |
Named /. elara in Westwood’s list, which otherwise
agrees. Unsexed.
Heteroscada gazoria, Godt.
10. 11. 25. g¢ =129, Minas Geraes.
Westwood’s list agrees. He calls the specimen “ Napeo-
genes?” in list, but on the insect itself he had written
“Yanina, Hew. f. 116, pl. 19, vol. ii. Hew. Exot. butt. Euri-
tea, Dry., not Cramer.” Unsexed.
Heteroscada yanetta, Hew.
Bz. 335. 17. 15.10.25. ¢ =180. MinasGeraes. (As 36.)
Agrees with Westwood’s list. Named Napeogenes. Un-
sexed. ‘Coll. Hew. but not named” in pencil indicates an
unsuccessful reference to his friend Hewitson.
Heteroscada fenella, Hew.
29. 10. 25. 9 =181. Minas Geraes. (As 72.)
Agrees with Westwood’s list “ Lent. Hewitson.” The
name “ fenella, H.” written in pencil by Westwood across
Burchell’s label. Unsexed.
Melinea paraiya, Reak.
8.2.26. ¢=182, Organ Mountains. (As 10-12.)
On a Weasel from the Atlas Mountains. 323
Agrees with Westwood’s list, where, however, it is named
as a var. of egina. Mech’. egina” is written on a label
attached to the specimen. Unsexed.
Melinea egina, Cram.
“7.7.29. $= 188. Pard. (As 107.)
28.7.29. ¢=184. Pard.
Be: 2601.30, (f= 13ab. © Pard:
Agrees with Westwood’s list. Unsexed,
Melinea ethra, Godt.
8. 2.26. ¢g = 136. Organ Mountains. (As 10-12.)
Agrees with Westwood’s list. Named by him Mech, ethra.
Sex unnoted.
Methona themisto, Hiibn.
14. 7.29. ¢=187. Pard.
laf 20.02 dae loos td9,,. Para,
Westwood’s list indicates the former existence of a fourth
specimen captured at Paré on 30. 7. 29. His name agrees.
Sexes unnoted.
[To be continued. ]
XXXVIII.—Note on an undescribed Weasel from the Atlas
Mountains, and on the Occurrence of a Weasel in the
Azores. By G. E. H. Barrett-HAMILTON.
THROUGH the courtesy of the Director and Officials of the
British Museum of Natural History, [ am enabled to publish
a short description of a weasel which is clearly distinguish-
able from the forms recognized by me in my paper published
in this Journal in January 1900.
This form, which may be known as Putortus nivalis atlas,
is remarkable for its size and robustness, in which it is per-
haps only excelled by the true P. x. africanus of Desmarest.
On the other hand, the line of demarcation between the
colours of the upper and under surfaces, a highly character-
istic feature in the weasels, is widely different from that of
P. n. africanus and other forms with a similar arrangement,
such as P.n. numidicus, P. n. boccamela, and P. n. sub-
palmatus, and allies it to P.n, ebericus and P. n. siculus.
In its tail, however, which carries a distinct terminal “pencil”
324 On the Occurrence’ of a Weasel in the Azores.
of dark brown hairs, it resembles P. n. numidicus and P. n.
africanus. ; ;
Colour.—Above between “ mummy-brown”’ and ‘ Mars
brown ” *, the under-fur a shade lighter. Below, except the
lower surface of the tail, but including the inner and lower
surfaces of the fore legs, the soles of the fore feet, and the
inner and lower surfaces of the hind legs almost down to the
ankles, white slightly washed with yellow. ‘The line of de-
marcation is decided, and runs on each side directly from a
point slightly anterior to the angle of the mouth to its
debouchment at the shoulders and thence to the hind legs.
The upper surfaces of all four feet are white for a distance
of about 13 and 11 mm. in the case of fore and hind feet
respectively from the base of the claws. In the hind feet
the white colour only just reaches the soles at their external
borders. The tail is brown above and below, and terminates
in a moderately developed “pencil” of longer hairs of a
deeper shade than the rest of the upper surface. There is
no trace of white on the ears. |
The dimensions of the hind foot and ear, both taken from
ihe type specimen when in spirit, are 42 and 21:5 mm. re-
spectively. No record was taken of the lengths of either
head and body or tail in the flesh, but the latter reaches a
length, including the terminal hairs, of 98 mm. in the dried
skin.
The skull, although strongly built, massive, and with
sagittal and lambdoid crests well developed, is less so than
that of P. n. africanus of the Azores. The postorbital pro-
cesses are moderately prominent, the nasal region moderately
broad and depressed anteriorly, and the posterior narial
aperture narrowed. ‘The incisive foramina are elongated,
having a length of about 2 mm., and recall those of the P. ermi-
neus group. ‘The following are the dimensions (in milli-
metres) of the type:—Greatest length 48; basal length 44:5 ;
greatest breadth at zygoma 26 ; palatal Jength 20.
The type, a female, no. 2.1.7.4 of the British Museum
Collection, from the Atlas Mountains, Morocco, was presented
by Mr. E. G. Meade- Waldo.
Opportunity may here be taken to point out that the
specimens recently received by the British Museum bear out
the opinion, some time since expressed by Professor J. V.
Barboza du Bocage t, that Desmarest’s type specimen of
* Names of colours printed in inverted commas are taken from
Mr. Robert Ridgway’s ‘ Nomenclature of Colors,’ 1886.
+ Jornal de Sci. Math., Phys. e Nat. ser. 2, no. xiii, (Lisbon, 1895)
pp. 24-27.
Bibliographical Notice. 325
P. africanus came, not from Egypt, but from the island of
St. Thomas, in the Gulf of Guinea, where there occurs a
form of weasel indistinguishable from the above type. The
naine africanus will therefore be most naturally applied to
the weasel of St. Thomas and to a similar form of which
Mr. W. R. Ogilvie-Grant recently procured a specimen at
Terceira, in the Azores, leaving the name subpalmatus, Hem-
prich and Hhrenberg, the exact allocation of which has long
been uncertain, for the weasels (formerly known as P. afrt-
canus) of Egypt and Malta. ‘The true africanus is now
shown to be a far larger and stronger animal than P. n.
subpalmatus, and it possesses a far more distinct caudal
“ pencil” of dark brown hairs. It has a wavy line of de-
marcation, and the inuch restricted white colour of the under
surface is strongly washed with deep “ buff-yellow.” The
dimensions of the Azorean specimen reach, for the animal
measured in the flesh, head and body 266, tail 116, hind
foot 44, and ear 18 mm.; and for the skull, greatest length 49,
basal length 45°5, greatest breadth at zygoma 28, and
palatal length 21 mm. It was caught in a rat-trap, which
had been set for a buzzard,
The occurrence of a weasel on the Azores must be re-
garded as a fact of considerable interest from the point of
view of the student of geographical distribution, still more
so as the animal is quite distinct from any known form
inhabiting Europe or the adjacent portions of Africa. That
a similar and undistinguishable weasel should be found on
the remote Island of St. Thomas is somewhat surprising, but
it seems a plausible hypothesis that the latter stock may have
been derived by introduction from the former.
BIBLIOGRAPHICAL NOTICE.
Report on the Sea Fisherves and Fishing Industries of the Thames
Estuary. Prepared by Dr. Jamns Murie. London: 1903.
Printed by order of the Kent and Essex Sea Fisheries Committee.
Tus report reflects great credit on the enthusiastic naturalist who,.
almost unaided, has accumulated in its pages an extraordinary mass.
of original and well-arranged information. Much has been done of
late years for the improvement of the scientific aspect of our sea.
fisheries, but the Thames estuary had been entirely neglected.
After introducing his readers to the physical formation of the
Thames estuary and to the history of Leigh-on-Sea, the fishing-
station where his observations have been made, the author deals
successively with the various members of the fauna which are in
some way or other of commercial importance—Seals. and Cetaceans.
326 Geological Society.
Food-fishes, Oysters, Mussels and other Molluscs, Shrimps, Lobsters,
and Crabs, all receiving due notice from both the life-history and
economical points of view. Some of these subjects are treated
with a profusion of details, much of which is entirely original,
which raises Dr. Murie’s contribution to a high scientific level.
The compilation of a vast amount of scattered information respecting
rare occurrences will prove a great boon to workers on the distri-
bution of fishes on our coasts—a subject on which much remains
to be done.
The chapter dealing with the Herring family (Clupeide) is a most
important piece of work, and the contribution therein on White-
bait adds greatly to our knowledge of a question which has been
frequently discussed before and since Dr. Giinther settled the question
by ascertaining the Whitebait of the Thames to consist mainly of
young herrings. Dr. Murie has taken great pains to ascertain the
nature of the mixed series of small fish &c. which are sent collec-
tively to the market under this commonly known appellation, and
he has added 20 to the 11 species which had already been listed
by Frank Buckland in 1879.
In dealing with the Weavers (Z’rachinus), so notoriously dreaded
by whitebaiters and shrimpers for their poisonous stings, the author
contributes a useful footnote recommending the best treatment in
case of accident.
Among the more remarkable fishes mentioned in the report,
Aphia pellucida, the White Goby, deserves special attention. It
was supposed to be rare in the district, but Dr. Murie finds it
astonishingly numerous, especially in March and April. According
to Prof. Collett, who has made a special study of this curious fish
in the Christiania Fjord, the adults die after breeding, and therefore
accomplish their life in the course of a year. Dr. Murie throws
doubt on this conclusion, for reasons which, however, are reserved
for a later communication.
In concluding this brief notice, we congratulate the Kent and
Essex Fisheries Committee on having had the good fortune of
bringing out a little book which will render such signal service,
and we look forward to the publication of further instalments of
the series of Reports of which the first is now before us.
PROCEEDINGS OF LEARNED SOCIETIES.
GEOLOGICAL SOCIETY.
November 18th, 1903.—Sir Archibald Geikie, D.C.L., D.Sc., F.R.S.,
Vice-President, in the Chair.
The following communications were read :—
1. ‘Notes on some Upper Jurassic Ammonites, with special
reference to Specimens in the University Museum, Oxford.’ By
Miss Maud Healey.
In the course of re-arranging the Upper Jurassic fossils in the
©5
Geological Society. |
Oxford University Museum, the attention of the Authoress has been
called to the large amount of prevailing misconception with regard to
Sowerby’s species Ammonites plicatilis and Am. bipler. The type-
specimen of Perisphinctes plicatilis (Sow.) is refigured and described.
It is in the form of a cast, but only an indefinite statement exists
as to the locality from which it was derived. It appears to be an
Upper Corallian form, and is usually taken as the zone-fossil of
that horizon. Sowerby’s two figures of Perisphinctes biplex repre-
sent different specimens, one of which is dismissed from consideration,
The other, probably from a Kimmeridge-Clay nodule found in the
Suffolk Drift, is refigured and described. The Authoress considers
that it would be wisest to abandon the name altogether, or at least to
restrict it to the abnormal specimen to which it was first attached.
The original specimen of Perisphinctes variocostatus (Buckland)
came from the so-called Oxford Clay at Hawnes, 4 miles south of
Bedford ; but the Authoress gives evidence in favour of her belief
that it was really derived from the Ampthill Clay. Sowerby’s
Ammonites rotundus is the last species figured, and it is doubtfully
identified as a variety of Olcostephanus Pallasianus (WOrb.). It was
derived from the Kimmeridge Clay of Chippinghurst, 64 miles
south of Oxford, and is the zone-fossil of the Upper Kimmeridge
Clay.
2. ‘On the Occurrence of Edestus in the Coal-Measures of Britain.’
By Edwin Tulley Newton, Esq., F.R.S., V.P.G.S.
This genus was originally described from the United States, and
was afterwards recognized in beds of similar age in Russia and
Australia. The genus was afterwards placed with Helicoprion
and Campyloprion in the family Edestidee. The specimen described
in the present paper was obtained by Mr. J. Pringle from one of
the marine bands which occurs between the ‘Twist Coal’ and the
‘Gin-Mine Coal,’ in the Smallthorn sinking of Messrs. Robert
Heath & Son’s pits at Nettlebank (North Staffordshire). Several
other marine bands, chiefly met with during the sinking of shafts in
this coulfield, have been studied by Mr. J. T. Stobbs, who called the
~ attention of the Geological Survey to the exposure from which this
specimen was obtained. The specimen is a single segment of a
fossil very closely resembling Hdestus minor, and consists of an
elongated basal portion, bearing at one extremity a smoothed,
enamelled, and serrated crown. A description of the fossil shows
that it is not to be referred to any existing species, and a new name
is giventoit. While it seems most in accordance with present
knowledge to regard the ‘spiral saw’ of Helicoprion as the enrolled,
symphysial dentition of an Elasmobranch, possibly allied to the
Cestracionts, it does not seem nearly so probable that the forms
referred to Hdestus are of the same nature. In the opinion of the
Author the latter are more likely to be dorsal defences. The paper
concludes with a bibliography of the subject.
328 Geological Society.
January 6th, 1904.—Sir Archibald Geikie, D.C.L., D.Sc., Sec.R.S8.,
Vice-President, in the Chair.
The following communication was read :—
‘Tmplementiferous Sections at Wolvercote (Oxfordshire),’ By
Alexander Montgomerie Bell, Esq., M.A., F.G.S.
This section shows the following beds:—(1) Oxford Clay ; (2) old
surface, in which are pits or troughs chiefly filled with gravel and
enveloped in weathered clay; (3) a large river-bed, containing gravel
at the base, and layers of clay above; (4) Neolithic surface-layer,
2 feet thick. The gravel of the river-bed contains quartzite-pebbles,
some of exceptional size, and is covered by a thin lenticular layer of
peat and sand, yielding thirty flowering-plants and many mosses; the
clays over this have probably been formed in a lake, possibly due to
a beaver-dam. In the grayel-bed are found implements formed of
flint quarried from the Chalk, or of quartzite from pebbles of the
Northern Drift, all remarkable for their size, beauty, and freshness,
together with the remains of large mammals, including the mammoth.
The old surface, from which the river-bed has been eroded, has
also yielded implements associated with quartzites, quartz-pebbles,
and lydianstone, gravel from the Thames Valley, limestone-pebbles,
Oolitic fossils, and sand. This deposit is regarded as remanié
from the Northern Drift, probably laid down under the action
of ice, as shown by the flask-like shape of the pits, the vertical
position of some of the pebbles, and the jamming-in of masses
of sand, probably in a frozen condition. Further, the Oxford
Clay beneath the surface is weathered and shaken to a depth
of 10 or 12 feet, except where cut off by the descending depth of
the river-bed. The implements are small, ordinary in shape, and
made of flint, not quarried, but mostly taken from the Drift, and.
they are much weathered, stained, and patinated. The occurrence
of an older set of implements, differing so markedly from those of
the river-drift, leads the Author to explain the peculiar imple-
mentiferous drift of Iffley as containing implements of two kinds
and two dates. Those that are unweathered are contemporaneous
with the deposit, and like those of the Wolvercote river-bed ; while
those that are stained with ochre, or deeply patinated, have been
derived, like the Oolitic fossils, Tertiary conglomerate, quartzites,
and volcanic rocks, from an older deposit. The Author believes
that the frequent occurrence of weathered and unweathered im-
plements in a single deposit may be explained generally in this
way; and he further infers that the time between the Drift and
the River-bed was prolonged, and that the interval may have been”
as long as that which separates the epoch of the River-bed from the
present day, his evidence being simply the patination of the flints.
In conclusion the Author suggests that there are three classes of
implement-bearing drifts, the ice-drifts being the earliest and the
river-drifts the latest, while the wash-drifts may belong to more
than one stage.
Ann. & Mag. Nat. Hist. S. 7. Vol. XIII. Pl. VI.
André & Sleigh, Limited.
All the figures ave the natural size.
Butterflies Captured in Brazil,
By W. J. BURCHELL (1825—29), with the corresponding manuscript labels.
THE ANNALS
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]
No. 77. MAY 1904.
XXXIX.—The Phylogeny of the Teleostomi.
By C. Tate Reaan, B.A.
[Plate VIL.]
In the following paper I have tried to give an account of the
phylogeny of the main groups of the Teleostomi, based on
the evidence of the available morphological data. In forming
my conclusions I have been helped by criticism and advice
from Mr. Boulenger and Dr. W. G. Ridewood, to both of
whom I gratefully express my acknowledgments. I trust
that the reasons given for differing from the classifications
~ hitherto proposed will prove sufficient: the aim of this paper
is constructive rather than destructive, and I have not thought
it necessary in every case to give all the available arguments
against theories of relationship which I do not accept, but
have rather tried to establish the ideas of phylogeny which
are here put forward ona sound morphological basis.
The class Pisces, as usually understood, comprises Verte-
brates with jaws, with gills supported by visceral arches, and
with paired limbs in which the endoskeletal supports have
not yet attained the pentadactyle arrangement of higher
Vertebrates. Two subclasses may be recognized—Chondro-
pterygii and ‘Teleostomi. The latter are distinguished by the
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 22
330 Mr. C. T. Regan on the
_ development of membrane-bones, including an operculum *
covering the chamber into which the gill-clefts open.
The Teleostomi may be divided into five orders, the rela-
tions of which are expressed in the following diagram :—
Teleostei,
/
/
Dipneusti. Placodermi,
ae 7
Crossopteryg!. ie
ino.
Chondrostei.
The Chondrostei and Crossopterygii correspond to the
groups usually so named; the Dipneusti comprise the
Sirenoidei only ; the Placodermi include the Arthrodira,
Antiarcha, and Osteostraci; and to the Teleostei the Ganoidei
Holostei are added.
These orders may be defined as follows :—
Order 1. CHONDROSTEI.
Median fins with the dermal rays in greater number than
their endoskeletal supports, which are typically in two prin-
cipal series, baseosts and axonosts, with an outer series of
small marginal cartilages. Caudal typically completely
heterocercal (rarely abbreviate heterocercal or diphycercal).
Paired fins not notably lobate. Pectoral baseosts articulating
with an anterior coraco-scapular cartilage and a_ posterior
metapterygium f. Ventrals with a well-developed series of
baseosts articulating internaily with a series of axonosts,
which may be separate or more or less completely fused.
Hyostylic. Hyomandibular without posterior process for
* In some specialized forms (e. g. Aspredinide) the operculum is
wanting.
+ It is impossible to say whether in the most primitive Teleostomi the
metapterygium was already developed or whether it was represented by
a series of separate axonosts,
Phylogeny of the Teleostomt. 331
the articulation of the operculum; symplectic not ossified.
Branchiostegals not attached to epihyal and ceratohyal.
Gular plates, if present, not specially enlarged. Clavicle
distinct from the cleithrum. Notochord persistent. Peri-
cardium * communicating with the coelom,
Order 2. CROSSOPTERYGII.
Median fins with the dermal rays often in greater number
than their endoskeletal supports, which are often in two
series. Caudal heterocercal or diphycercal. Pectorals
lobate, with metapterygium often segmented. Ventrals lobate
or not, with supports variously arranged. Hyostylic. Bran-
chiostegals replaced by a pair of large gular plates. Clavicle
distinct from the cleithrum. Vertebral column variously
developed.
Order 3. DIPNEUSTI.
Median fins with the dermal rays in greater number than
their endoskeletal supports, which are in two series. Caudal
heterocereal or diphycercal. Paired fins acutely lobate,
with endoskeletal supports arranged as a segmented axis with
or without lateral branches. Autostylic, the palato-quadrate
being fused with the cranium and the hyomandibular reduced
or absent. Sometimes a pair of large gular plates, but
branchiostegal rays never present. Clavicle not distinct from
the cleithrum. Notochord persistent.
Order 4. PLACODERMI.
Median fins membranous, without dermal rays, consisting
of a single dorsal, supported by regular series of baseosts and
axonosts, and a heterocercal caudal. Pectoral fin, if fune-
tional, represented by a jointed Arthropod-like limb, with
internal muscles and external dermal plates, sometimes
reduced to a fixed spine, or absent. Ventral fin, if present,
with a series of baseosts and a single large axonostal cartilage.
? Autostylic. Notochord persistent. Usually a well-deve-
loped dermal armour.
Order 5. TELEOSTEI.
Median fins with the dermal rays equal in number to their
endoskeletal supports, which are typically in one series, the
* T have taken this character from Bashford Dean, ‘ Fishes Living and
Fossil,’ p. 260,
22%
332 Mr. C. T. Regan on the
baseosts being either small or absent. Caudal abbreviate
heterocercal, homocercal, or diphycereal. Paired fins usually
not lobate. Pectoral metapterygium sometimes well deve-
loped and serving for the articulation of the posterior
baseosts, more often reduced and apparently forming the first
of the baseost series. Ventral with the dermal rays directly
attached to a single basal bone, the baseosts rudimentary or
absent. Hyostylic. Hyomandibular with a posterior process
for the articulation of the operculum ; symplectic ossified and
usually suturally united to the quadrate. Branchiostegal
rays attached to the epihyal andceratohyal. No paired gular
plates. Clavicle not distinct from the cleithrum., Vertebral
column variously developed. No communication between
pericardium and ccelom.
It need hardly be pointed out here that I cannot expect the
characters used in the above ordinal definitions to prove
constant in every case. Experience shows that, however
well defined groups may seem to be, as our knowledge of
them becomes more complete annectent forms come to light,
and it is self-evident that if we were acquainted with all the
forms which have existed we should have a perfect phylo-
genetic arrangement, but no division into groups. Conse-
quently the generalizations which I have made may or may
not be applicable to those unsatisfactorily known extinct
forms (e.g. Catopteride) which can only be provisionally
assigned to a position in the system.
CHONDROSTEI.
The Chondrostei, which have been regarded by some as
modified Crossopterygii, are undoubtedly the most generalized
of all Teleostom1.
The ventral fins of Polyodon, Actpenser, and Scaphi-
rhynchus have been well described and figured by Thacher *
in 1877, and also by Davidoff + in 1879, the former of whom
regarded their structure as most important evidence of the
truth of his theory of the similar origin of the median and
paired fins. This view was also accepted by Bridge t, who,
in 1878, referring to Polyodon, wrote:—‘‘'The evident
formation of the ventral fins by the coalescence of a series of
* Tr. Connect. Ac. iv. 1877, p. 234, pls. 1. & i.
+ Morph. Jahrb. v. 1879, p. 450, pl. xxviii, See also Wiedersheim,
* Gliedmassenskelett,’ p. GO (1892).
{ Phil. Trans, elxix. 1878, pp. 683-734.
Phylogeny of the Teleostomi. 333
originally distinct cartilaginous rays is clearly indicative of a
more primitive condition of these structures than can be found
in any other living vertebrate animal.”
The Chondrostean ventral fin having been thus described
as principally composed of a series of basal cartilages
(baseosts) supporting the dermal rays, articulated internally
to another series of cartilages (axonosts) which exhibited
some fusion anteriorly, it was inexcusably careless of Cope *
to propose a classification ignoring this, his order Podopterygia
(7. e. Chondrostei) being characterized as possessing median
fins with numerous axonosts, pectoral without uxonost and
rudimentary baseosts, and ventral with one axonost and
several baseosts. In Smith Woodward’s classification T,
which is based on that of Cope, the structure of the paired
fins in the Chondrostei has also remained unappreciated.
Finally Traquair {, in discussing the evolution of fishes,
whilst paying considerable attention to the paired fins of
Crossopterygii and Dipneusti, does not even think them
worthy of notice in the comprehensive order Actinopterygil.
So that it would almost seem as if the structure of the paired
fins in the Chondrostei, of the highest importance in any
discussion as to the affinities of that order and of the very
greatest interest as evidence in favour of the lateral fin fold
theory, although well known to the morphologists, is in
canger of being forgotten by the systematists.
‘The ventral fins of Psephurus gladius are even more
primitive than those of Polyodon §, and as they have not yet
been described, so far as I am aware, I propose to do so and
to compare their structure with that of the anal and pectoral
tins. All three fins—pectoral, ventral, and anal—strongly
resemble each other in external appearance, being extended
and composed of numerous articulated dermal rays, at the
base of which there is in each case a similar muscular lobe
projecting beyond the body-wall, and in which the series of
baseosts is imbedded.
On dissection the anal fin is seen to be supported by a
series of cartilages, baseosts, 21 in number, which articulate
internally with a similar series of axonosts. The latter,
* Am. Nat. xxi. 1887, p. 1017.
+ Cat. Foss. Fish. (4 vols. 1889-1901) and Vert. Palzeont. (1898).
¢ Presidential Address to Zool. Section of Brit. Assoc. (1900),
§ St. George Mivart, in 1879 (Tr. Z.S. x. p. 457), described and
figured the anal fin of Polyodon as the ventral, the mistake being due to
a wrongly labelled specimen in the Museum of the College of Surgeons,
but it is curious to note that on receiving T'hacher's paper he did not
realize this, but supposed the difference to be due to individual variation.
334 Mr. C. T. Regan on the
however, are reduced in number to 18, owing to the fusion of
the first 8 and the next 2. The ventral fin is supported by a
series of 12 baseosts, exactly similar to those of the anal,
which also articulate with a series of axonosts, which in this
case are 8 in number, owing to the fusion of the anterior 5.
In both anal and ventral the cartilages of the ‘“ baseost”’
series, or radials, show a tendency to segment into 3, thus
forming proximal, median, and distal series of segments,
whilst external to the last, and completely overlapped by the
dermal rays, are a series of short “ marginal” cartilages.
In the specimen described the anal fin is 23 mm. in length
and is composed of 70 dermal rays supported by 21 baseosts,
whilst the ventral is 11 mm. in length and is composed of
38 rays supported by 12 baseosts, a proportionate correspond-
ence sufficiently close to be remarkable.
I would submit, then, that the extremely similar structure
of the anal and ventral fins in Psephurus can only be
explained on the theory of a directly similar origin, and that
the theory that the structure of the anal is primitive, whilst
that of the ventral is derived in some way from a biserial
archipterygium, is fantastic and entirely unsupported by
evidence. ‘Ihus, in an actual living species we have clearer
and more complete evidence of the similar origin of the
median and paired tins than in the extinct Cladodus, which
las been considered so important.
The pectoral fin of Psephurus is more specialized than the
ventral; the baseosts are 7 in number, the anterior 3 being
attached to the large coraco-scapular cartilage, which repre-
sents tle fused anterior axonosts and which underlies a
membrane-bone, the cleithrum. ‘The posterior axonosts are
also fused to form a single cartilage, the metapterygium. In
other living Chondrostei the pectoral fin is very similar to
that of Psephurus, whilst in the ventral fin the extent of fusion
cf the axonosts and the number of the baseosts show some
variation. In the Palwoniscide, so far the earliest and most
generalized Chondrostei known, the ventral fins often had an
extended * base and were composed of numerous rays. In
one genus, the Liassic Coccolepis, a series of baseosts have been
discovered. The axonosts have not so far been distinguished,
but there is every justification for believing that in this
generalized family fins so similar to those of Psephurus
had their supports arranged in the same primitive manner.
As regards the pectorals, the coraco-scapular cartilage with
* It is interesting to note that in the Devonian genus Cheirolepis the
ventral fin is longer than the anal.
Phylogeny of the Teleostom@. 395
the overlying cleithrum must be regarded as typical of the
ancestral T’eleostome; whether the fusion of the posterior
axonosts also is corelated with this, or whether the meta-
pterygium was represented in the early Teleostomi by a series
of separate axonosts, there is no evidence to show, but the
structure of the pectoral in all Teleostomi is easily explicable
as a modification of that of Psephurus.
In the structure of their median, as well as of the paired
fins, the Chondrostei are essentially primitive, and the con-
dition of the vertebral column also bears witness to their low
position. It appears to me fairly well established for both
living forms and for those extinct ones which undoubtedly
belong to this order that the hyomandibular does not develop
a posterior process for articulation with the inner face of the
operculum, as is the case in all Teleostei.
Fig. 1—Diagrams to show the arrangement of the branchiastegals and
gular plates in a typical Crossopterygian, Chondrostean, and
Telecst. A. Rhizodopsis sauroides (after Traquair) ; B. Rhabdo-
lepis macropterus (alter Traquair); C. Amza calva. 0.g., inter-
gular; y., gular plates; /g., lateral gulars ; 6., branchiostegals ;
c.h., cerato-hyal; s.op., suboperculum ; m2., lower jaw.
In the Palezoniscide the arrangement of the plates supporting
the gill-membranes and extending forward between the man-
dibular rami, as described by Traquair *, is one from which the
conditions which obtain in other ‘l'eleostomi are readily deriv-
able. On each side there is a continuous series of obviously
homologous plates, the upper two or three of which are en-
larged as the opercular bones, those following being the bran-
* Mon. Paleont. Soc., Paleoniscide, p. 21 (1877).
336 Mr. C. T. Regan on the
~ chiostegals, the anterior pair of which are considerably larger
than the rest and may be termed “ gular plates.” In front of
the gular plates there is sometimes an unpaired “ intergular.”
The anterior branchiostegals and the gular plates occupy
the whole of the space between the mandibular rami, to which
they are apposed, whilst each meets its fellow in the middle
line. Within the order Chondrostei the gular plates and
branchiostegals may disappear, but we never get the con-
ditions characteristic of either Crossopterygii or Teleostei.
We have only just begun to realize that the clavicles
proper (infraclavicles) which Parker thought he recognized
in so many Teleostean fishes (Siluride, Hemibranchii, Lopho-
branchii, Ostracton) are entirely wanting in that group, and
the presence of this bone as a distinct element in the Chon-
drostei and Crossopterygii becomes therefore of ordinal value.
The arrangement of the bones of the cranial roof in the
Chondrostean Paleoniscide is essentially similar to that of
the more generalized representatives of the other orders
(the Dipneusti excepted). Assuming the interfrontal pineal
foramen to be a primitive structure, we may expect to discover,
a Paleoniscid-like fish possessing this feature, and had such
a one existed in the early Silurian it would have been in
every way fitted to become the progenitor of the ‘Teleostomi.
CROSSOPTERYGII.
The Crossopterygii are modified Chondrostei, from which
order the more generalized forms differ but slightly. The
lobate pectoral fin has been shown by Dollo * to be an adaptive
specialization, and is not to be regarded as of greater import-
ance than the lobate pectoral of some Teleosts (e. g. Perio-
phthalmus, Pediculati) ; it may easily have been derived from
the Chondrostean type in the following manner :—
The pectoral fin began to be used at times as a support for
the body, and even as an ambulatory limb. ‘This change of
function produced a changed orientation in the muscular lobe
at the base of the fin, which, originally parallel to the body-
wall and attached to it for its whole length, became set at an
angle to the body and detached from it posteriorly. As the
Jobe separated the dermal rays extended round on to its inner
side. The arrangement of the skeletal supports scarcely
* Bull. Soc. Belg. Géol. ix. 1895, p. 79.
+ I am by no means satisfied that the pectoral fin of the extinct
genera Tristichopterus and Eusthenopteron is correctly described as uni-
basal. That of Tristichopterus, as originally described and figured by
Phylogeny of the Teleostomt. 337
changed, but the metapterygium became segmented (or this
segmentation may be primitive, each segment representing an
axonost). From such an asymmetrical fin the symmetrical
fins of Ceratodus would be derived by an increase in length
of the lobe and of the number of axial segments and the
development of posterior cartilages for the support of the
inner series of dermal rays. ‘he evolution of the ventral
fins would be on similar lines.
ee
MLL” MUU
Fig. 2.—Diagrams to illustrate the evolution of lobate paired fins ; the
axonosts are unshaded, the baseosts shaded 1, primitive con-
dition; 2 and 5, stages seen respectively in ventral and pectoral
of Acipenser; 4, obtusely lobate fin; 5, pectoral of Polypterus ;
6, acutely lobate fin.
In the pectoral fin of Polypterus there are two basal
pieces articulated to the coraco-scapular ossifications, which
Traquair (Tr. R. Soc. Edin. xxvii. 1876, p. 383, pl. xxxii. fig. 9), would
seem to consist of an axis (metapterygium) of three segments an1 of three
baseosts, of which the first appears to be attached to the coraco-scapular.
338 Mr. C. T. Regan on the
are inserted close together and diverge distally. Of these
the posterior, metapterygium, is the longer, whilst the shorter
anterior one is the first baseost. Polypterus is peculiar
among Crossopterygii in that the metapterygium is not split
up into or followed by a series of segments, whilst the baseosts
are numerous and are attached to the distal edge of a lamina
which has developed between the two basal bones, and in
which an ossification has arisen. Nevertheless this type of
fin does not appear to me to justify the proposal which has
been made to regard the Cladistia as a distinct order,
As to the structure of the ventral fins of the Crossopterygil,
in those forms in which they were non-lobate this was
probably as in the Chondrostei, and the modern Polypterus
has an arrangement similar to that which is sometimes seen
in Scaphirhynchus—t, e., a single basal piece supporting a
short series of baseosts. ‘There is evidence, too, that the
supports of the obtusely lobate ventrals were very similar to
those of the obtusely lobate pectorals.
The replacement of the branchiostegal rays by the develop-
ment of the paired gular plates is a characteristic feature of the
In Lusthenopteron the same arrangement has been described by Whit-
eaves (Tr. R. Soc. Canada, 1888, p. 87). Before I had seen either of
these descriptions I had formed the opinion that the so-called “ basal
cartilage” in the pectoral of Eusthenopteron figured by Smith Woodward
(Vert. Paleeont. p. 25, fig. 25) was probably coraco-scapular, on account
of its shape and bulk, and it appears to me to bear a most suspicious
resemblance to the ossification named coraco-scapular by Traquair in
Tristichopterus and to the coraco-scapular of the recent Polypterus. The
so-called postaxial process would then be the downwardly projecting
portion of the coracoid ; otherwise it seems to me to be inexplicable, since
the dermal rays do not appear to extend so far, and if such a proces
developed on the basal segment, why not on the second ?
The alternative supposition, which is the one apparently now adopted
by Smith Woodward and Traquair (Geol. Mag. 1890, p. 19), is that this
bone is the basal segment of the axis. If this be so, then it follows that
in the specimens of Tristichopterus on which Traquair’s description was
based this large bone had not been preserved or was hidden.
Unless we assume that Polypterus originated independently of other
Crossopterygii, it seems to me clear that the primitive Crossopterygian
must have had a pectoral in which the first baseost retained its attach-
ment to the coraco-scapular, for I regard the theory that the acutely
lobate symmetrical fin has given rise to the obtusely lobate asymmetrical
fin as exploded, and I shall require more satisfactory evidence than has yet
been forthcoming to convince me that this condition is not realized in
Tristichopterus or Eusthenopteron, as would appear from the original
description of each.
I must add that I have been in correspondence with Dr. Traquair, who
has very kindly told me that he is not inclined to accept my view, which
I put forward here merely for the purpose of stating a case.
\ es
a aay
Phylogeny of the Teleostomi. 339
Crossopterygii, but the supposed homology of the lateral gulars
with the branchiostegals is doubtful. As has been pointed out
above, in the Paleoniscide the gular plates and branchiostegal
rays are serially homologous, whereas the Crossopterygian
lateral gulars are plates developed between the principal gulars
and the mandibular rami. Moreover, whilst the Paleoniscid
branchiostegals are so imbricated that each overlaps the one
in front of it, the lateral gulars exhibit precisely the reverse
arrangement. Nevertheless, in the Devonian Palseoniscid
Cheiroleyis, as figured by Traquair *, the anterior branchio-
stegal extends forward between gular plate and lower jaw,
and this might be regarded as leading to the Crossopterygian
condition.
In the Crossopterygii we see the development of the bone
which Boulenger has shown to be the representative of the
squamosal of higher Vertebrates. This is fused with the
preoperculum in Polypterus, but coexists with it in several
extinct forms, and corresponds to the upper bone of the
postorbital (as distinct from the circumorbital) series of the
Paleoniscida. The bone internal to it, which is the one
usually called squamosal in fishes, is without doubt the true
supratemporal f, and should be so named throughout the
‘Teleostomi, whether or no it includes a ‘ pterotic”’ ossification
in certain Teleosts, whilst the series which lie posterior to the
parietals and true supratemporals might be termed dermo-
occipitals, thus avoiding confusion with the true supraoccipital.
Many Crossopterygii have a pineal foramen, a feature as
yet undiscovered in any Chondrostei, and they must have
evolved in the Silurian from some primitive type belonging
to the latter order.
DIPNEUSTI.
The relations of the Dipneusti to the Crossopterygii have
been elucidated by Dollo ¢ in a convincing essay. He gives
good reasons for believing that Dipterus is the most generalized
ot all Dipneusti, and that it has originated from a Crosso-
pterygian type closely allied to Holoptychius. It is only
necessary to add here that his views as to the specialized
character of the lobate paired fins receive additional con-
firmation from the demonstration of the primitive nature of
the non-lobate paired fins of the Chondrostei.
* Ann. & Mag. Nat. Hist. (4) xv. 1875, p. 237,
+ This conclusion is not invalidated by the fact that Polypterus has no
supratemporal, the bone so named by boulenger being the “ accessory
hyomandibular ” of ‘Traquair.
| Bull. Soc. Belg. Géol. ix. 1895, p. 79.
340 Mr. C. T. Regan on the
PLACODERMI.
The close relationship of the Coccosteide and Asterolepidx
had been generally recognized until they were so widely and
unnecessarily separated by Cope, a proceeding which has
found more support than it deserved, and I have no hesitation
in uniting the groups of which these families are represen-
tative, together with the Osteostraci, in a single order of
Teleostomi. It has been stated that the bones of the skull
of the Coccosteide cannot be homologized with those of
other Teleostomes ; but, as has recently been pointed out by
Jexkel *, if we take a generalized type such as Coccosteus, the
Fig. 5.—Diagrams to show the arrangement of the bones of the cranial
roof in Coccosteus (A) and in a typical Crossopterygian (Rhizo-
dopsis) (B) (both after Traquair). m.o., median dermo-occipital ;
l.o., lateral dermal occipital; p., parietal ; 7, frontal; ptf, post-
frontal ; s.¢., supratemporal ; pin., pineal; eth., ethmoid; pme.,
preemaxillary ; so., suborbital ; op., operculum.
cranial roof-bones are arranged as in a generalized Crosso-
pterygian or Stegocephalian. Posteriorly we see the three
large dermo-occipital plates which we so frequently meet
with in the Rhizodontide and Osteolepide. In front of these
are the paired parietals and frontals, the latter bounding the
orbits laterally and partly separated medianly by a pineal f
* Sitzb. Ges. naturf. Berlin, 1902, p. 108.
+ The pineal plate occupies the position of the pineal foramen of
some Osteolepids.
Phylogeny of the Teleostomi. dL
plate. Paired postfrontals and supratemporals are well
developed, whilst anteriorly a median ethmoid separates the
premaxillaries. A single large bone on the cheek which
sends forward a process below the orbits represents the
sub- and postorbitals, and may include the maxillary also.
The opercular bones are represented by the operculum only.
The nostrils are lateral, between pramaxillary and ethmoid.
Gular plates and branchiostegal rays are apparently wanting.
In the arrangement of the bones of the cranial roof Coccosteus
is almost a typical Crossopterygian, and the arrangement of
the supports of the dorsal fin in two regular series and the
structure of the ventral fin, which appears to be essentially
similar to that of Polypterus *, cannot be said to negative this
view.
A comparison of Coccosteus with Pterichthys shows the
following important points of agreement :—
(1) The anterior part of the trunk is enclosed in an armour
of bony plates which are not united to those of the
head, so that the latter is freely movable.
(2) There is a single dorsal fin which is membranous.
(3) There is a single cpercular bone ¢ and a pitted pineal
bone.
(4) The dermal armour } ts in both cases composed of dense
bone with a cancellated structure in its thicker portions,
with an outer layer of ganotne, with a tuberculated
surface, and with open grooves for the sensory canals.
(5) The arrangement of the bones of the head, but espe-
cially that of the dermal plates of the body, can
easily be reduced to a common plan.
In the skull of Pterichthys we recognize posteriorly the
three dermo-occipitals, the supratemporals, and the operculum
of Coccosteus, whilst anteriorly the median ethmoid and
laterally the large suborbital plate are still in the same relative
positions. The premaxillaries are now entirely on the lower
surface, but, as in Coccosteus, they seem to border the nostrils.
The orbits have approached each other until they are only
separated by the pineal plate. ‘he postfrontal is fused with
the suborbital.
If Jekel be correct in regarding Homosteus as intermediate
* It is noteworthy that Coccosteus resembles Polypterus in the position
of the nostrils also.
+ In both cases this bone has been interpreted by some authorities as
other than opercular, so that it would be perhaps better to say “there isin
both a similarly placed bone which may be regarded as an operculum.”
{ See Smith Woodward, ‘ Vertebrate Paleontology,’ p. 12 (1898), and
Cat. Foss. Fish, ii. p. xix (1891), :
342 Mr. C. T. Regan on the
between Coccosteus and Pterichthys, then the frontals have
been displaced forwards and have either disappeared or
become fused with the ethmoid or with the suborbital plates,
and the so-called postmedian represents the parietals. On
the other hand, there is the possibility that this element may
be frontal in origin and that the median dermo-occipital may
include the parietals, and I incline to this latter view.
Fig. 4.—Ventral plates of trunk-armour of (A) Pterichthys (after Tra-
quair) and (B) Coccosteus (atter Traquair). 7./., interlateral ;
s., lateral spine; p., pectoral limb; a@.m.v., anterior median
ventral; p.m.v., posterior median ventral; a.v.l., anterior
ventro-lateral; p.v.l., posterior ventro-lateral. The faint lines
indicate the extent of the overlap; the suture between the
interlateral and the lateral spine in Coccosteus has been inserted.
The arrangement of the plates of the armour of the trunk
is on a very similar plan in both Coccosteide and Astero-
lepide, 1 or 2 median dorsal plates, 1 or 2 pairs of anterior
and posterior lateral plates, and on the ventral surface 4 large
plates in exactly the same position and oyerlapping each
other and a smaller four-sided median piece in a very similar
manner, whilst a small anterior median plate may or may
not be present. The semilunars of the Asterolepide seem to
correspond to the elements (interlaterals) which have been
regarded as clavicles in the Coccosteide.
The case of Acanthaspis may be cited as evidence of the
similarity of the plates of these two families in structure and
arrangement. This genus, according to Smith Woodward *,
* Vert. Paleeont. p. 16,
a
Phylogeny of the Teleostomi. 343
“has a dermal armour resembling that of the Antiarcha in
minute structure and a ventral plastron quite similar to that
of the latter. The lateral appendages, however, instead of
being complex and movable, are simple and fixed.” Never-
theless Traquair* has given good reasons for regarding
Acanthaspis as a Coccosteid, and it would even seem that the
fixed spinous appendage may be diagnostic of that family.
So far, then, Coccosteus has been shown to resemble the
more generalized Crossopterygii in the arrangement of the
bones of the cranial roof, and reasons have been given for
regarding the Asterolepide as closely related to the Cocco-
steide fF.
What, then, of the peculiar pectoral limb of the Astero-
lepide ? It has been sometimes assumed that this is not
homologous with the pectoral fin of other fishes, but evidence
in support of this assumption has not been forthcoming.
Bashtord Dean even goes so far as to say that these ap-
pendages are now known to be the lateral head-angles [? of
Cephalaspis] produced and jointed for locomotion. his
extraordinary theory is evidently based on a complete mis-
conception as to the position of the Asterolepid limbs, and so
needs no discussion. Smith Woodward seems to think that
the fixed spinous appendage of Acanthaspis in some way
supports the view of the independent origin of the Asterolepid
pectoral, and I suppose therefore that he regards it as a stage
in the development of the latter. Personally, I am unable to
imagine that a fixed spine could possibly give rise to a jointed
Arthropod-like limb with internal muscles. In fact, the
structure of such a limb, articulated to an anterior plate of
the body, in which latter is a large foramen, indicating that
tendons, blood-vessels, and nerves passed to the muscles of
the limb from the body, postulates for me an unarmed ancestor
with a muscular limb already developed. Just as the
similar limbs of the Crustacea are generally held to have been
* Geol. Mag. (3) x. 1893, p. 148.
{ The reasons which haye been given for regarding Coccosteids and
Asterolepids as not related are (1) the more vascular bone of the latter,
(2) the presence of specialized paired fins in the former, and (3) the well-
ossified Jaws of the Coccosteids. With regard to these, the resemblances
in the structure of the bony plates are very remarkable, and the differences
are evidently not well marked, or there could be no doubt as to the
position of a genus after the minute structure of the bone had been ascer-
tained. The Asterolepid pectoral is surely specialized enough, and it is
purely gratuitous to assume its non-homology with that of other fishes,
As to the non-ossified lower jaw of the Asterolepids, instances are not
wanting in Chondrostei and Teleostei of degeneration of membrane-hones
or of the reversion of a bone to its primitive cartilaginous condition,
j44 Mr. C. 'T. Regan on the
derived from the Annelid parapodia, muscular projections
used in progression, by increase in size accompanied by
hardening and segmentation of the exoskeleton, so do I con-
ceive the Asterolepid limb to have been derived from the
lobate Crossopterygian pectoral fin, already being used to
support the body and for ambulatory progression, by the
development of dermal plates on the muscular lobe of the fin
at the same time that the anterior part of the trunk became
armoured. ‘The fixed spinous appendage of the Coccosteidze
seems to represent the pectoral limb of the Asterolepida, so
that we may regard the former as the more generalized in
the structure of the skull, the latter in that of the pectoral
limb.
We now pass to the Cephalaspide and the related forms
included in the Osteostraci. The reasons for regarding these
as allied to the Asterolepide have been given by Smith
Woodward, and they appear to me sufficient and convincing,
and may be briefly summarized here. In both groups we
have a similar caudal region, with a single dorsal fin in the
same position and with the caudal fin heterocercal, with a
well-developed lower lobe. ‘Then, again, in two Osteostracan
genera, T'remataspis and Didymaspis, the anterior part of the
trunk is enclosed in armour, consisting of a dorsal shield to
which a ventral shield is opposed, the dorsal shield being
distinct from the head-shield in the former genus, but fused
with it in the latter. Since the head-shield is continuous,
the nostrils must have been inferior, as in the Asterolepide,
whilst the orbits are approximated and separated only by a
pineal plate, as in that family. Finally, the exoskeleton is
composed of true bone in its inner layers, as in other
‘Ganoid”’ fishes. Where I differ from Dr. Smith Wood-
ward with respect to this group is that whereas he looks
upon the genera which most nearly approach the Asterolepide
as the most specialized, J regard them on that account as the
most generalized, and the loose pineal plate and the ganoine
layer of Tremataspis appear to me in favour of my view.
Conceived as specialized and degenerate Asterolepide, the
structure of the Osteostraci is easily explicable, but I cannot
reconcile the Asterolepid structure with the idea that they are
a further development of the Osteostraci or of anything like
them, whilst if the resemblances between Asterolepide and
Coccosteide are due to convergence (as they must be if they
belong to different subclasses), then morphology has ceased to
be a guide to relationship. Finally, the Heterostraci must
be considered, since they have often been associated with the
j
/
Phylogeny of the Teleostomi. 345
Cephalaspide, although it has long been known that they
differ from them fundamentally in the microscopic structure
of their dermal armour, bone lacune being entirely absent,
whilst there is great similarity to the tooth-structure of the
Elasmobranchs. Lankester has strongly maintained that the
Tfeterostraci and Osteostraci are an unnatural association,
and as long ago as 1867 he wrote *:—“ The Heterostraci
are associated at present with the Osteostraci because they
are found in the same beds, because they have, like Cepha-
laspis, a large head-shield, and because there is nothing else
with which to associate them—the shields are not so closely
similar in plan, much less in histological structure +, as to
warrant any inference of similarity in other parts.” Within
the last few years Traquairt has discovered new forms
which seem to place it beyond doubt that the Heterostraci
are armoured Chondropterygii. He has also discovered a
new genus, Afeleaspis, which he considers is annectent
between Heterostraci and Cephalaspidie, but this view I am
not prepared to accept. Ateleaspis is certainly very closely
allied to Cephalaspis, but I cannot see that there is the least
reason for regarding it as allied to anything else. The
shield is divided superficially into hexagonal areas, which are
compared to those of Cephalaspis, in which genus this
appearance has been shown by Lankester§ to be due to the
ariangement of the vascular canals, which may even cause
the shield to crack along these lines, whilst in pl. x. fig. 5, a
specimen of Cephalaspis asper is figured in which the polygonal
areas are very strongly brought out by the great pressure and
the infiltration to which the shield has been subjected. If
Lankester is correct, and the polygonal areas of Cephalaspis
are due to the arrangement of the vascular canals, then they
are not due to the coalescence of originally separate poly-
gonal pieces, as suggested by Traquair, who believes he has
found in Afeleaspis a stage in this development. Traquair’s
idea that the superficial tubercles of the shield of Ateleaspis
represent originally separate Ccelolepid denticles appears to me
* Mon. Palzont. Soc., Cephalaspide, p. 62 (1867).
+ The difference in structure of the dermal armour of Pteraspis and
Cephalaspis is essentially that between a “ placoid” and a “ganoid” scale.
There is no reason why the former should not have given rise to the
latter and to membrane-bones, by fusion and by the development of a bony
substratum, more than once. On the other hand, the evidence shows that
the Teleostomi, as here understood, are monophyletic.
{ Trans. Roy. Soc. Edinburgh, xxxix. 1899, p. 827 et seg., and Rep.
Brit. Assoc. 1900, p. 773.
§ ‘ Cephalaspide,’ p. 10.
Ann. & Mag. N, Hist. Ser. 7. Vol. xiii. 2a
346 Mr. C. T. Regan on the
still less valid, and might be applied with equal force to any
of the numerous Ganoid fishes with tuberculated bones, and
surely it is a retrograde step to suggest that structures which
in Cephalaspis have been shown to be posterior extensions of
the head-shield may after all be pectoral fins.
In fact, the evidence that the Coccosteide are Teleostomi,
that the Asterolepide are allied to the Coccosteide, and that
the Cephalaspide have been derived—through the Trematas-
pide—from the Asterolepide, is so clear, that I am com-
pelled to regard the Ateleaspid structure as a modification of
that of the Cephalaspid.
TELEOSTEIL.
The reasons for regarding the Teleostei and Chondrostei as
distinct orders and for including the Holostei with the former
are apparent in the diagnoses given above. The Holostei
may then be regarded as the first Teleostean suborder*, dis-
tinguished from the Malacopterygii by their well-developed
splenial and by one or more of the pectoral baseosts being
attached to the metapterygium. Whether certain features of
resemblance between Polypterus and the Holostei, of which
the articulation of the operculum to a posterior process of the
hyomandibular is the most important, are to be interpreted as
derived from a common ancestor or as due to convergence is
not yet clear.
Tur PALZONTOLOGICAL EVIDENCE.
It may be said that the conclusions as to the evolution of
the Teleostomi expressed above are not in accordance with
the palxontological evidence; but to this I reply that they
are in accordance with the morphological evidence, which is
clear and sufficiently complete, whilst the geological record is,
and must be from the nature of the case, very incomplete.
The Teleostomi probably originated from Pleuropterygian
Elasmobranchii in the Lower Silurian, and the Crossopterygii,
with their specialized offshoots the Dipneusti and Placo-
dermi, must have rapidly evolved, since all are well represented
in the Lower Devonian, and the highly specialized Cepha-
laspide are found in the Upper Silurian. In the same way
that generalized Reptilia gave rise to the host of forms which
* Provisionally, for I am inclined to think that none of the characters
which have been used to distinguish between Holostei and Malacopterygii
will prove satisfactory.
Phylogeny of the Teleostomt. 347
were characteristic of the Secondary period, including the
highly specialized Ichthyosauria and Pterosauria, which
declined and were replaced by a new race, the Mammalia,
derived also from the same generalized stock, so must we
conceive the primitive Teleostomi as giving rise to the
Crossopterygii, with their specialized offshoots the Dipnenst1
and Placodermi, and remaining dormant to develone later on
into the typical Chondrostei. There is no justification for
regarding the Crossopterygii as less specialized than the
Chondrostei because they were the earlier dominant group.
The non-recognition of the true position of Cephalaspis as a
specialized Asterolepid seems to have been due to its occur-
rence in the Upper Silurian ; but when we consider that, in
spite of the imperfect geological record, we know that types
so divergent as Chevrolepis, Tristichopterus, Holoptychius,
Dripterus, Coccosteus, Homosteus, Pterichthys, and Cephalaspis
were already in being in the Lower Devonian, we may feel
assured that some of these, and numerous annectent forms
also, must have existed long before.
SUMMARY AND CONCLUSIONS.
The main results of the foregoing paper may be stated as
follows :—
(1) The Chondrostei are the most generalized Teleostomi.
(2) The Crossopterygii differ from them
(a) in the lobate pectoral fin ;
(6) in the larger paired gular plates.
(3) The Placodermi (Coccosteide, Asterolepida, Cephalas-
pide) are a natural group, not related to the Heter-
ostraci, which are Chondropterygu. They may
probably be regarded as armoured primitive Crosso-
pterygii, this view being most in accordance with
(a) the arrangement of the cranial roof-bones in
Coccosteus ;
(b) the structure of the ventral fin in Coccosteus ;
(c) the structure of the pectoral limb of the Astero-
lepidee.
(4) The Dipneusti probably originated from more specialized
Crossopterygii, e. g. from the neighbourhood of the
Holoptychiidee.
(5) The ‘eleostei differ in so many respects from the
Chondrostei that they should rank as an order, in
which the Holostei are included,
23*
348 On the Phylogeny of the Teleostomt,
Tn the Teleostomi and the Chondropterygii * the evolution
of the paired fins has proceeded independently, but sometimes
on parallel lines, from the earliest stages. ‘The median fins
of the Teleostomi also tend to undergo the same modifications
as the paired ones, but this comparison must not be pushed
too far. The most primitive condition is that which we have
seen in the anal and ventral fins of Psephurus: (1) dermal
rays much more numerous than the baseosts, which form a
well-developed series, attached internally to a series of
axonosts, the anterior of which show a tendency to fusion.
From this stage is easily derived that which is seen in the
anal fin of Lusthenopteron, or in the ventral of Polypterus
or ? Coccosteus, 7. e. (2) dermal rays more numerous than
the baseosts, which are attached to a single cartilage or bone
formed by the fusion of the axonosts. The third stage (3),
in which the baseosts are rudimentary or absent and the
dermal rays are attached direct to the axonostal bone, is
exemplified in the anterior dorsal of the Ceelacanthide and
the ventrals of the Teleostei.
Two conditions met with in the median fins are not
paralleled in the paired ones. The first is a modification of
stage (1) described above, and is that seen in the Teleostei,
baseosts small or wanting, dermal rays equal in number to
the axonosts. ‘lhe second is derived from stage (2), and is
that seen in the posterior dorsal of Holoptychtus, in which
there is a single axonostal cartilage, whilst the baseosts are
numerous, crowded, and apparently subdivided, some being
attached to others instead of to the axonost.
Similarly the paired fins undergo modifications which
* Thacher (Tr. Conn. Ac. iii. & iv. 1877) deduced the theory of the
similar origin of median and paired fins from their similar structure in
the Elasmobranchii and Chondrostei. Balfour, from a study of Elasmo-
branch development, also deduced the similar origin of median and paired
fins. Heconcluded that in modern Elasmobranchii the ventral fin retains
in all essential respects its primitive arrangement, and that the pectoral
metapterygium represents the pelvic basipterygium. He also wrote: “I
should be much more inclined to hold that the fin of Ceratodus has been
derived from a fin like that of the Elasmobranchii by a series of steps
similar to those which Huxley supposes to have led to the establishment
of the Elasmobranch fin, but in exactly the reverse direction.”
I prefer these conclusions to the more recent ones of Cope and Smith
Woodward, who regard the fins of modern Flasmobranchii and Chon-
drostei as highly specialized, and I would point out that the Ichthyotome
pectoral must have been derived from the Pleuropteryzian type in the
same way as the paired fins of the Dipneusti from those of the Chon-
drostei, the axis, or metapterygium, representing the series of axonosts,
and not being derived from an elongate baseost.
On Lleteropiera from the Transvaal. 349
cannot be paralleled in the median ones, when the axonosts
form the axis of a lobate fin, and these have already been
discussed in treating of the order Crossopterygii.
EXPLANATION OF PLATE VII.
Fig. 1. Anal (A.), ventral (V.),and pectoral (P.) fins of Psephurus gladius,
the two last from the ventral or inner aspect.
Fg. 2. Thesame, dissected to show thesupporting cartilages. cor., coraco-
scapular ; mt., metapterygium ; a., axonosts; 7., baseosts (radials) ;
m., marginals,
XL.—Rhynchotal Notes—XXIUI. By W. L. Disranr.
HETEROPTERA FROM THE TRANSVAAL.
Tue British Museum has secured a set of the specimens of
Rhynchota collected by the Rev. H. A. Junod at Shilouvane,
Zoutpansberg, Northern Transvaal, and this paper refers to
undescribed species found in the collection, ‘The Capsida
have already been described (ante, p. 196 et seqg.), while the
Homoptera, poorly represented, are reserved for future treat-
ment. ‘lhe greater part of the Zoutpansberg district possesses
a subtropical climate and is much covered with bush and
dwarf forest, thus being in strong contrast with the high and
barren veld which constitutes so large a portion of the T'rans-
vaal landscape. I was therefore not greatly surprised to tind
both many new species and others known in entomological
record, which I had neither seen nor secured during four
years’ collecting in other parts of the Transvaal. Two
genera, Geomorpha and Phonolibes, both hitherto represented
only by asingle West-African species, are now found to have
each a representative species in North Transvaal.
All the types are contained in the National Collection.
Fam. Pentatomide.
Subfam. Crpyrvz.
Gnathoconus elongatus, sp. n.
Elongate; black ; lateral margins of pronotum, basal half
of lateral margins of corium, second and base of third joints
of antennz, tibiee (excluding apical third), lateral margins of
the fourth, fifth, and sixth abdominal segments, and the apical
350 Mr. W. L. Distant on
margin of anal segment to the abdomen pale ochraceous ;
a large discal spot to corium creamy white; lateral lobes of
the head very thickly finely punctate ; pronotum (excluding
the transverse callose area and lateral margins), scutellum,
and corium somewhat coarsely punctate ; membrane pale
bronzy.
Allied to G. tibialis, Stal, also found in the Transvaal, but
much more elongate ; pronotum with the lateral margins
continuously narrowly ochraceous, but basal margin con-
colorous ; apex of scutellum concolorous, &c.
Long. 5 mm.
Geomorpha Junodi, sp. n.
Fuscous brown; head, anterior area of pronotum, and legs
testaceous ; a narrow, transverse, callose fascia to pronotum
at about one third from anterior margin, and central fused
spots to fourth and fifth abdominal segments, ochraceous ;
connexivum piceous, the marginal tubercles ochraceous ;
membrane obscure brownish ochraceous, with piceous suffu-
sions; head moderately long, profoundly sinuate in front of
eyes, lateral lobes longer than central lobe, a little outwardly
iy upwardly dilated at their apices, which do not quite
neet; antenne mutilated in typical specimen; pronotum
Sane and somewhat transversely rugose behind the pale
transverse callose fascia, the anterior area with some very
coarse punctures, the lateral angles very broad, obtusely
angularly prominent ; scutellum short, broad, its base trian-
gularly elevate, continued in a central carination to apex, its
surface strongly rugose, with four small obscure ochraceous
spots on basal area; corium opaque, coarsely punctate, its
lateral margin about as long as, and its inner margin only
extending a little beyond middle of, scutellum ; membrane
reticulate, not quite reaching apex of abdomen ; body beneath
considerably suffused with ochraceous.
Long. 10; exp. pronot. angl. 74 mm.
Fam. Coreide.
Subfam. Corzm.
Division PETASCELARIA.
Carlisis serrabilis, sp. n.
Head above and antenne black; basal annulations to
second and third joints of antenna, a central fascia to head
beneath, and rostrum (excluding apex) ochraceous ; pronotum
Heteroptera from the Transvaal. 351
either piceous suffused with ochraceous, or ochraceous suffused
with piceous, extreme anterior area piceous, beyond which is
a transverse ochraceous line, three abbreviated longitudinal
ochraceous lines at base, the lateral margins always black or
piceous ; scutellum black, its central lateral margins, apex,
and a central longitudinal line more or less obscurely ochra-
ceous ; corium ochraceous, much suffused with piceous or
black; membrane black; connexivum black, spotted with
ochraceous, the spots bifid above; body beneath and legs
black, opaque; anterior and anterior lateral margins and a
central fascia to prosternum, a central fascia to mesosternum,
a broad central spot to metasternum, and lateral margins of
corium as seen beneath, ochraceous ; anterior and intermediate
femora (excluding apices), an obscure central annulation to
tibie, and the second joint of tarsi testaceous. First and
fourth joints of antenne subequal in length, second and third
joints longer and almost subequal; pronotum sparingly
punctate, with its lateral margins very coarsely serrate for
their whole length ; scutellum transversely wrinkled ; corium
very sparingly punctate; anterior and intermediate femora
denticulate beneath near apex, posterior femora incrassate,
obtusely convexly dilated at about middle of inner margin ;
anterior lateral margins of corium blackly granulate.
Long., ¢ ¢, 26-28 mm.
Division GONOCEBARIA.
Plinachius trilineatus, sp. n.
Head ochraceous, obscurely punctate, with three longitu-
dinal black lines—one central, the other two from near base
of antenne to ocelli; antenne with the first, second, and
third joints castaneous, fourth pale fuscous, with its base
ochraceous ; pronotum ochraceous, thickly brownly punctate,
extreme lateral margins and the posterior lateral angles
castaneous ; scutellum ochraceous (excluding margins and
apex), blackly punctate; clavus stramineous, blackly punc-
tate; corium subroseus, blackly punctate; membrane dark
bronzy brown ; body beneath and legs ochraceous; a spot on
each side of pro-, meso-, and metasterna, and three basal
spots on each side of second, third, fourth, and fifth abdominal
segments black ; first, third, and fourth joints of antenne
subequal in length, second longest; rostrum reaching the
intermediate coxe ; lateral pronotal angles acutely spinous,
their apices directed a little forward.
Long. 17 mm.
352 Mr. W. L. Distant on
Subfam. Aryprv#.
Mirperus nigrofasciatus, sp. n.
Ochraceous, coarsely punctate; a lateral fascia on each
side of head, two discal longitudinal fascie to pronotum
(not reaching anterior margin), a large central spot and
narrow sublateral fascia to mesonotum, two longitudinal fascie
to abdomen and between them on basal area two narrower
and ill-defined fascia, black; legs piceous, with ochraceous
suffusions ; corium with the punctures thickly black towards
apical area and the lateral margins stramineous; membrane
pale piceous, its apical margin pale hyaline; antennz with
the first, second, and third joints brownish ochraceous, fourth
joint mutilated, first and second joints subequal in length,
third longest; rostrum piceous above and reaching inter-
mediate cox; the punctuation very coarse and strong on
pronotum, more finely punctate on scutellum and corium ;
head finely granulate; posterior femora in male incrassate
and spined beneath, two subapical spines longest; posterior
tibie strongly curved, almost as long as femora.
Long. 94 mm.
Alirperus robustus, sp. n.
Dull ochraceous, darkly punctate ; head and anterior area
of pronotum thickly greyishly pilose; membrane greyish
brown, with scattered small piceous spots; head beneath,
disk of sternum and two oblique fascize on its apical areas,
a central and a waved fascia on each side of abdomen beneath,
apex of rostrum, and the femora black ; an oblique line and
a small basal spot on each side of head beneath, tibia, and
antenne dull ochraceous; annulations to anterior and inter-
mediate tibie, bases and apices of posterior tibie, and apices
of tarsi black; basal joint of antenne shorter than head,
about equal in length to second joint ; rostrum reaching the
intermediate cox; connexivum ochraceous, spotted with
black.
Lone. 9 mm.
Fam. Lygeide.
Division ORSILLARIA.,
Nysius rubromaculatus, sp. n.
YJ » Sp
Head, anterior area of pronotum, and scutellum testaceous,
pronotum (excluding anterior area) ochraceous; a spot on
Lleteroptera from the Transvaal, 353
head near each ocellus, centre of anterior margin and a sub-
basal line to pronotum, and basal margin of scutellum black ;
corium pale hyaline, its apical angle broadly reddish testa-
ceous ; membrane pale hyaline, its apical area suffused with
testaceous and piceous ; body beneath testaceous; legs stra-
mineous, apices of femora and tibiz a little darker ; antenne
ochraceous, basal joint and apex of second a little darker,
second, third, and fourth joints subequal in length, basal
joint shortest, not reaching apex of head; head strongly
attenuated and laterally sinuate in front of eyes; pronotum
very coarsely punctate ; scutellum with a subbasal transverss
carination, which is centrally continued to apex.
Long. 4a mm,
Division APHANARIA.
Aphanus atomarius, sp. n.
Ochraceous, thickly punctured with brown ; head reddish
ochraceous, lateral margins and apex, margins of central lobe,
two large basal spots, and eyes black ; pronotum with. black
lines enclosing an irregular transverse space on anterior area,
the lateral margins moderately laminately reflexed ; scutellum
with a black line occupying nearly centres of lateral margins
and two longitudinal black lines at apex; corium with the
apical angle black ; legs ochraceous ; abdomen beneath casta-
neous ; head beneath, ‘disk of sternum, a central longitudinal
fascia to abdomen, anterior femora (excluding apices), apices
of intermediate and posterior femora, and apices of tibize and
tarsi black. Antenne mutilated in the six specimens now
before me.
Long. 5-55 mm.
Allied to A. orientalis, Dist., from British India,
Fam. Reduviide.
Subfam. Sreworopinz,
DITHMARUS, gen. nov.
Body moderately elongate, a little posteriorly widened ;
head subeylindrical, not narrowed anteriorly and between an-
tennz armed with two porrect spines, eyes inserted at about
one third from base, behind and between which the surface is
transversely tuberculate and there contains the ocelli, extreme
base narrowly pedunculate; antenne strongly pilose, first
joint nearly as long as head, second twice as long as first ;
354 Mr. W. L. Distant on
rostrum reaching the anterior coxee, first and second joints
subequal in length; pronotum rather more than twice as
broad at base as at anterior margin, transversely constricted
at middle, centrally longitudinally broadly excavated, lateral
aa sinuate, posterior angles acutely prominent, anterior
angles shortly subtuberculously prominent; apex of scutellum
produced in a somewhat long semierect spine; hemelytra
reaching apex of abdomen, the last with its margins a little
dilated ; abdomen beneath flatly depressed, but witha very
strong central longitudinal ridge; anterior angles of pro-
sternum shortly spinous ; legs of moderate length, anterior
femora strongly incrassate and shortly spinous beneath.
Allied to Argolis by the two anterior spines to head, but
differing by the incrassate and spinous anterior femora.
Dithmarus atromaculatus, sp. n.
Cinnamon-brown; antenne and legs stramineous; clavus
and anterior area of corium of a creamy hue; membrane slaty
grey; an elongate spot to clavus, a broken discal spot
and a larger apical spot to corium, and a very small basal
and a large discal spot to membrane black; connexivum
spotted with creamy white; anterior femora beneath mode-
rately suffused with piceous; the tarsi and apices of tibia
ochraceous.
Long. 17 mm.
Subfam. Harpacrorrn 2.
Phonolibes bimaculatus, sp. n.
Black, greyishly pilose ; base and apex of head, two rounded
discal spots and margins of lateral angular areas to pro-
notum, margins and central carina to scutellum, connexivum,
posterior margin to prosternum, lateral margins of meso- and
metasterna, cox, trochanters, and abdomen beneath san-
guineous ; lateral areas of abdominal segmental incisures and
anal abdominal segment black ; first joint of antenne about
as long as head and subequal in length to third, second short,
about half the length of third.
Long. 93 mm.
Allied to the West-African P. venustus, Stal, from which
it differs by its smaller size and altogether different markings ;
the pronotum is also narrower and much less profoundly
longitudinally impressed.
fleteroptera from the Transvaal. 355
Harpactor femoralis, sp. n.
Black ; legs and lateral margins of abdomen testaceous ;
apices of femora, bases and apices of tibize, and the tarsi
black ; first joint of antenne about as long as head ; anterior
lobe of pronotum broadly centrally sulcate towards its base,
posterior lobe obscurely granulate ; scutellum foveate at base,
its apex robustly porrectly produced ; legs longly pilose ;
first joint of rostrum about reaching eyes, second joint about
twice as long as first.
Long. 124 mm.
Sphedanolestes corallinus, sp. n.
Coral-red ; corium and anterior and intermediate tibie dull
ochraceous ; antenna, eyes, apex of head, ocelli and a short
line behind them, outer area of corium, posterior tibia, apices
of anterior and intermediate tibia, and the tarsi black ;
membrane pale hyaline ; ‘first joint of antennae about as long
as pronotum and scutellum together ; both lobes of pronotum
centrally longitudinally suleate ; membrane passing apex of
abdomen ; femora moderately nodulose.
Long. 8 mm.
Endochus cinnamopterus, sp. n.
Cinnamon-brown ;_ body beneath, connexivum, rostrum,
and legs pale ochraceous; lateral pronotal angles black ;
head almost as long as pronotum, transversely constricted
between the eyes, first joint of antenne bright castaneous and
about as long as anterior femora, its apex and the second and
third joints ochraceous; rostrum with the first and second
joints almost subequal in length ; pronotum transversely con-
stricted before middle, the anterior area a little sculptured and
medially impressed, the posterior area sparingly ochraceously
pilose, posterior margin truncate, the lateral posterior angles
shortly, laterally, spinously produced ; membrane _ pale
bronzy ; apices of femora and the whole of anterior and
intermediate tibia cinnamon-brown ; abdomen not angularly
dilated, beneath with lateral series of small black spots, one
on each segment ; head on each side behind base of antenne
tuberculate, but not spinous.
Long. 21-22 mm.
Lindochus straminipes, sp. v.
Fuscous brown ; body beneath and legs stramineous ; head
356 Miss Cora B. Sanders on the Rhopalocera
slightly shorter than pronotum, with a rather long semierect
spine a little behind the base of each antenna; first joint of
rostrum distinctly longer than the second ; first joint of an-
tenna stramineous, about as long as anterior femora, remaining
joints mutilated ; pronotum elongate, finely transversely con-
stricted before middle, the posterior lobe finely granulate,
posterior lateral angles longly, spinously, laterally produced ;
corium a little darker in hue and iinely greyishly pilose ;
membrane bronzy ; abdomen moderately angularly dilated on
each side at the junction of the fifth and sixth segments ;
legs somewhat longly pilose.
Long. 135 mm.
XLI—The Collections of William John Burchell, D.C.L., in
the Hope Department, Oxford University Museum.
IV. On the Lepidoptera Rhopalocera collected by W. J.
Burchell in Brazil, 1825-1830. By Cora B. SANDERS,
of Lady Margaret Hall, Oxford.
999
[Concluded from p. 323. ]
Il. Dawarn.
Anosta erippus, Cram.
Bz. 122. I. 15. 8. 25. @=140. Rio de Janeiro. “In a
cross-lane about halfway between the Gloria Hill and.
Botafogo Bay. All found on plants.” “Papilio.”
10. 1.26. @=141. Rio de Janeiro. Prdia Graénde and
S. Joao de Carahy.
27. 1.26. 9 = 142. Rio de Janeiro.
31.1. 26. g¢=1438. Riode Janeiro. (As 66.)
26. 2. 26. 2 @=144, 145. Near Fréchal and the Rio Magé.
Brazilian date and later copy on 145.
1. 3. 26. 2 9 = 146,147. (As 121.) Brazilian date and
later copy on 147,
13. 3.26. @=148, RiodeJaneiro. “From Magé. a.[M.].”
13..3. 26. 9 = 149. Rio de Jangiresi< Ai,
1.4.26. @=150. Rio de Janeiro. ‘In the Valley of
Catumbi.”
3.4.26. 9=151. -Rio de Janeiro. ‘‘ Along the Carioca
Aqueduct.”
23.°9. 2672 @ = 152; 15e.- Santos.
collected by W. J. Burchell in Brazil. 857
Bz. 3.11. 26. ¢=154. Santos. “On Monserrat.”
12.11. 26. 9 =155. Santos. “In the Forest above the
Monastery of Sao Bento.”
Bae Ge 29 f= 156? * Para.
16. 6. 29. 2 6 = 157, 158. Pard. Brazilian date and later
copy on 157.
25. 6. 29: 9 = 159. Parad:
4.7.29. g= 160, (75
Do Fes 2 Oe St tOds "55
1507. JA. 7.29. 6= 162. Pard.
Bz. 1397.+ 14. 7. 28. = 1624. Paré. A g Danaine pupa-
case from which the butterfly had emerged. Obviously
the pupa of 162.
23.7, 29. Both dates and both |
numbers written > = 1628, 162c. Pard.
14.7. 99, thus on one label.
Two ? Danaine pupe which had.died. The species is
probably the same as 162 A. Both are much gnawed, perhaps
by parasites, perhaps at a later date by Anthreni. Both pupze
on a single pin, which bears an original Brazilian label with
the number 7397 in addition to the later label with the two
numbers and the two dates.
Soe. 9 = 16oq Bard:
The remaining lists in this paper were not in Westwood’s
handwriting.
The dates agree, except that the former existence of four
or, perhaps, five additional specimens is indicated ; another
with the data of 149, another with those of 159, a specimen
with the number 737, captured on 16. 8. 25 (Rio. Above
the Theresa Convent; and on the woody hill [or hills] along
the Aqueduct”), and one captured on 30. 10. 25 (Minas
Geraés. “In the forest. On the N.E. side of the arraial of
Sao Jofio de Népomucéna.”) The date 5. 7. 29 follows
4, 7. 29 in the list without the usual intervening mark which
indicates a separate individual. Its insertion may be merely
a copyist’s error. If, however, this is not the case, the
additional specimen was captured at Pard. The only name
given in the list is Danais.
Beyond this point no reference to sex indicates that no
determination is given in the list,
Tasitia gilippus, Cram.
z.110. I. 15.8. 25. 9 =164, RiodeJaneiro. (As 140.)
Bz. 900. [.4+ 25. 10.25. ¢= 165. Minas Geraes. (As
37, 38.)
358 —— Miss Cora B. Sanders on the Rhopalocera
31.12.25. ¢ = 166. Rio de Janeiro. ‘ Excursion to the
Summit of the Corcovado; from Catéte and up the valley
of Laranjeiros.”
26.1. 26. ¢=16%. Rio de Janeiro. “In a botanical and
entomological excursion to the Barra Vermelha, Morro
de Ladeira and Catombi.”
27.1. 26. 9 = 168. Rio de Janeiro.
1. 3226. .¢ = 169: “Mace: (Agden)
7.3. 26. 9=170. Riode Janeiro. “ At Catombi.”
923. 20. 2 aes, <
13.730 20te ge Ele, ao ‘ OAS Mee h
24,12. 26. 9 =173. Cubatio. “ At Rio das Pedras and
Cubatio.”
20. 8.27. 9=174. N.W. of Mogy Mirim. “ Urisénga
to Itupéba.”
Bz. 8.12. 28. 9 =175. Porto Real [Nacional].
29.1. 29. 2 6 = 176,177. Porto Real [Nacional].
Bz. 1309.+ 11. 2. 29. ¢ = 178. Porto Real [Nacional].
“ Papilio. The flight of this is remarkable, tor it does
not always hover by a constant motion of wings, but
frequently sails with wings half extended, without moving
them at all; nor is it very visible by what movement it
sails along.”
07. 2.29. 2= 179. Porto Real [iNaciwonalie
175 dee. 2s = IROL SL. va. x
D2. 29. 2 Go =A6e, Lod.) ‘5 Brazilian date
and later copy on 182.
Bz.+ 23.3. 29. 9 = 184. ,, 4
24. 3.29. g = 185. “i « Manga.”
98..5..29. 2g 186/186. a; o Brazilian date
and later copy on 187.
The dates in Westwood’s list agree, except that the former
existence of three additional specimens is shown, viz. another
of the same date as 164, another with the date of 180, 181,
and a specimen captured 2.3.29 (Porto Real=Nacional).
The fact that Burchell captured two specimens on 15. 8. 25
is also shown by his note-book. The only name given is
Danais.
[I was extremely interested to read Burchell’s note on
specimen no. 178, inasmuch as it exactly describes a common
mode of flight in the allied Danaine Anosta plextppus. I was
much struck with it in the Northern United States in the
summer of 1897, for I had never seen a butterfly sail in the
same manner before. The appearance produced by the half-
extended wings was singularly boat-like, the resemblance
being much increased by a continual oscillation from side to
collected by W. J. Burchell in Brazil. 359
side, like the roll of avessel. The underside of these Danainz
18 even more conspicuous than the upperside, and it occurred
to me that the significance of the peculiar attitude and move-
ment was to display the underside during flight. The
method adopted is probably the only means by which this
end could be achieved.—E. B. P.]
Lycorea halia, Hew.
10. 11. 25. = 188.. Minas Geraes.
31.12. 25. =189. Riode Janeiro. (As 166.)
Bz.+ 1.3. 26. = 190. Magé. (As 121.)
Bz. 10. 3. 26. = 191. Rio de Janeiro.
Bzul9, 5s 26, — £92, o “In the Valley of
Catombi.”
1. 4. 26. = 198. 5 “In the Valley of
Catumbi.”
30.10. 27. = 194, HE. of Goyaz. On road from Meia
Ponte. ‘ Conceicio.”
24, 12.27. = 195. Goyaz.
Name and dates agree with Westwood’s list, except that he
refers to a ninth specimen captured on 8. 2. 26, “ Organ
Mountains (in a ride to the Cattle Pounds and the Milho
Roga).”
[These specimens may afford a deeply interesting instance
of change in something under three quarters of a century,
or, on the other hand, the results may be merely due to a
deepening in the tint of a yellowish pigment owing to age.
Lycorea halia is an outlying member of Blandford’s
Group 3, “ East Brazilian Type,” Division (a), having “ the
apical spots on the fore wing yellow.”’ This important group
was shown by Mr. W. F. H. Blandford to the Entomological
Society in 1897 (see Proc. Ent. Soc. Lond., May 5, 1897).
It is mainly characterized by a bright yellow horizontal band
traversing the hind wing parallel with the inner margin of the
fore wing. The Lycorea, being an outlying member of the
group, has a pale yellowish band, which is very different from
the bright tint of the more centrally placed members, such as
the species of Heliconius. Now Burchell’s specimens are
far more removed from the group than those of recent date,
inasmuch as the band is but slightly paler than the tawny
ground-colour of the wing. In favour of the view that a
change has actually occurred and is here registered are the
following facts:—(1) the specimens are, as a whole, singu-
larly perfect ; (2) one specimen is lighter than the rest, its
band being of a shade common in recent specimens; (3) the
360 Miss Cora B. Sanders on the Rhopalocera
yellow band, the characteristic feature of the group, is a very
special and ’ peculiar one among the numerous patterns and
colour combinations of Neotropical synaposematic groups ;
(4) that a butterfly which is outlying to-day should be still
more outlying seventy-five years ago is not surprising. Rapid
change is more probable in a case of this kind than perhaps
in any other. On the other side it must be remembered :—
(1) that the yellow tints of some butterflies are very apt to
darken; (2) that similar dark forms of Lycorea halia are to
be found in collections of much less age, or even occasionally
in recent consignments.
The latter argument, of course, supports both sides of the
case.
It is not too much to hope that the question may be settled
by intentional exposure or other experiments upon the yellow
pigment of recent specimens, as well as by the investigation
of all available material.
Miss Sanders and I have already carefully compared the
Burchell specimens with the series at Oxford, in the British
Museum, and in the Godman-Salvin Collection, and there
can be no doubt about the existence of a marked difference
between the bands of the Burchell specimens as a whole and
those of more recently captured individuals of L. halia.
When in the later pages of this memoir the Heliconiins
belonging to the same group are recorded, it will be con-
venient to reproduce typical examples of as many members
as possible by the best photographic processes which we
can command. I think that the differences of shade can be
accurately rendered in this manner and made available in a
half-tone plate.—H. B. P.]
Jtuna tlione, Cram.
Bz. 12. 11, 26. = 196. ‘Santos. ¥“" Forest by 8. Bento.2
Date and name as in Westwood’s list.
III. Sarrvrimz.
Pierella lamia, Sulz.
13. 5. 29. 2 6 = 197,198. Rio Tocantins, Carolina. ‘Boa
Vista in Sylva densa” on 197%. There are two Brazilian
labels on 198: “ Sylva densa” on one, ‘ 13, 5. 29 Boa
Esper” on the other.
Date as in Westwood’s list, where, however, only one
specimen is mentioned. 198, a very poor specimen, was
collected by W. J. Burchell in Brazil, 361
found among duplicates and recognized by Burchell’s hand-
writing on the label. The printed “ Burchell Collection ”
label affixed to the specimens at Oxford was wanting.
When the name is not referred to, it is to be understood
that none is given in Westwood’s list.
Pierella nereis, Drury.
14,1. 26. ?=199. Rio de Janeiro. (As 29.)
14. 2.26. 9 = 200. Organ Mountains. Near R. Pacaqué,
Dates as in Westwood’s list.
Pierella astyoche, Erich.
ia 8.204 % =20!. Pars,
Date as in Westwood’s list.
Prerella lena, Linn.
Bz.+ 19. 5. 29. 2 = 202. Descent of Rio Tocantins.
Rio Araguay.
Date as in Westwood’s list.
Pierella dracontis, Hiibn.
Bz. + 24. 7.29) Y= 208. .. Para.
4.12.29. = 204. Pard, S. José.
Dates as in Westwood’s list.
Anchiphlebia archea, Hiibn.
12. 3. 26. ¢ = 205. Riode Janeiro. Carioca Aqueduct.”
Westwood’s list includes another specimen captured on
22. 8. 26 (Rio. “ Along the Aqueduct to the head of the
Valley of Laranjeiros’’).
Euptychia ocirrhoe, Fabr.
Bz. 190. I. 8. 9. 25. 9 = 206. Rio de Janeiro, “ Along
the Aqueduct. Papilio.”
31.12.25. g= 207. Riode Janeiro. (As 166.)
Bz.+ 7. 3. 26. ¢ = 208. Rio de Janeiro. “ At Catombf.”
9, 3. 26. 2 ¢ = 209, 210, 9 = 211. Riode Janeiro. Bra-
zilian date on 209.
10. 3.26. g@=212. Rio de Janeiro.
Pa. 202 2 = 219; + “Carioca Aque-
duct.”’
15. 3, 26. g = 214. 4 * Catombi. In
plantis.”
Piss. co = 2l0: + “In the upper part
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii 24
362 Miss Cora B. Sanders on the Rhopalocera
of the Valley of Catombi, and along the road thence to
Rio Comprido and Matto Porcos.”
17. 3. 26. 2 6 = 216, 217. Rio de Janeiro. “ Along the
Carioca Aqueduct, and descending the high hill men-
tioned (31. 1. 26) into the valley of Catombi. But they
were mostly along the Aqueduct, and only a few on
the hill.” Brazilian date on 217,
18. 3. 26. 9 = 218. Rio de Janeiro. Along the Carioca
Aqueduct.
Bz. 20. 3. 26. 9 = 219. Riode Janeiro. Along the Carioca
Aqueduct.
Bz. 21. 3. 26. 2 ¢ 2 = 220, 221. Rio de Janeiro. Along
the Carioca Aqueduct.
22.3. 26. $= 222. Rio de Janeiro. Along the Carioca
Aqueduct.
1. 4. 26. @= 228, Rio de Janeiro. (As 198.)
19.55. 29. 2.6 9 = 224, 225. (R. Tocantins. _ (As:202.)
7.'6.'29. 9 =226. °R. Tocantins. = Near Para) © “Sta.
Anna.”
1.8.29. § = 227. Pard.
18.9. 29. g= 228. Pard, 8. José. “In umbrosis Silve.”
24. 10, 29. ¢ = 289.) * 4 ty In Sylva.”
15. 11. 29. g= 2380. __,, + “Caminho de Cha-
ménte.”
Be.0.1.30, a= wel, Para.
All the twenty-six specimens here recorded agree with
Westwood’s list, but the latter also contains thirteen indi-
viduals which cannot now be found. Of these, five were
captured on dates unrepresented by existing specimens, viz.:—
one taken 7. 11. 25 towards the end of the expedition into
Minas Geraes, three taken at Rio on 13. 3. 26, 19. 3. 26,
3. 4. 26, and one taken at Goyaz (Caminho de Carreira) on
10. 4. 28 respectively. The remaining eight specimens are
made up as follows:—One more individual captured on
7. 3. 26, one more (viz. No. 1056) on 17. 3. 26, two more on
9. 3. 26, one more on 16. 3. 26, one more on 18. 8. 26, two
more on 20. 3. 26.
Although unnamed in the list, specimen 227 bears a label
with the name “ Huptychia ocirrhoe” written by Westwood.
Euptychia mollina, Hiibn.
1.8. 29. 2 9 = 232, 283. Pard. Brazilian date and later
copy on 233.
4,8. 29. °9' = 934. Pard.
5.8. BOT or BS5. op
collected by W. J. Burchell in Brazil. 363
8.8.29, 9 = 236. Para.
Bz. 15.11. 29. 2 29 = 287, 288. Paré. (As 280.)
Westwood’s list agrees, except that it mentions three addi-
tional individuals captured at Pard,— one on 4. 7. 29 and two
on 4, 12. 29, The name given is Neonympha mollina.
Euptychia herse, Cram.
Bz.+ 23.7. 29. $= 239. Paré. “ Between my house
and the city.”
Westwood’s list agrees.
EKuptychia chloris, Cram.
31.5. 29. ¢ = 240. R. Tocantins, near Paré. “ Baiio;
1 ae
Westwood’s list agrees,
Euptychia cosmophila, Hiibn.
20. 3. 26. = 241. Rio de Janeiro. Along the Carioca
Aqueduct.
This specimen was submitted to Dr. F. D. Godman, who
confirmed the identification.
Westwood’s list agrees.
Euptychia cluena, Drury.
10. 3. 26. 2= 242, 248. Rio de Janeiro.
1055. II. 17. 3. 26. 2= 244, 245. Rio de Janeiro. (As
216, 217.) ‘‘ Both these caught in deep woods, as the
preceding.” The latter refers to 351, and indicates cap-
ture “in the forest down the hill.”
18. 3. 26. 2= 246, 247. Riode Janeiro. Along the Carioca
Aqueduct. Brazilian date on 246.
20. 38. 26. 3= 248-250. Riode Janeiro. Along the Carioca
Aqueduct. Brazilian date on 248.
3.4. 26. =251. Rio de Janeiro. Along the Carioca
Aqueduct.
245 is probably the only female.
Westwood’s list agrees, except that the date 10. 2. 26 is
substituted for 10. 3. 26. This is almost certainly a mistake
of the copyist. It may be mentioned, however, that on the
former date Burchell was in the Organ Mountains.
Euptychia myncea, Cram,
10. 6:29, =.252, . Para.
20. tL. 29% = e00, Pat, 5.) Ose.
21%
364 Miss Cora B. Sanders on the Rhopalocera
Euptychia penelope, Fabr.,=clarissa, Cram.
Bz. 1332.4 2. 3. 29. =254 Porto Real [Nacional].
“Papilio. In woody places among the bushes. This
and its congeners fly in a very hovering zigzag manner
low among the bushes and herbage.”
Bz. 15, 3. 29. = 255. Porto Real [Nacional].
7.6. 29. = 256. R. Tocantins. (As 226.)
21 Tao Ps earns
15.11. 29. = 258. Pardé, S. José. (As 280.)
It is probable that the individuals of myncea and penelope
are considered together in Westwood’s list. The dates here
recorded agree, except that 10. 8. 29 (252) is replaced by
10. 2. 29, probably a clerical error. The list furthermore
includes individuals captured on 29. 12. 28 (Porto Real) and
18. 6. 29 (Para).
Euptychia sp.
28.5. 28. 2 § = 259 (Pl. VI. fig. 8), 260. Goyaz. “ Peak
near Cénta Gallo.” ‘In summitate montis.” Burchell’s
label, written in England, is reproduced to the right of
and below figure 8.
These specimens were submitted to Dr. F. D. Godman,
who is unable to name them. Mr. F. A. Heron considers
that the markings best agree with H. stmzis (Butl.), but he
points out that the eyes of the latter are hairy, while those of
259, 260 are naked. In the character of the distal end of the
cell of the fore wing these specimens also best agree with
similis and its allies, The marked development of the ocelli
on both wings is peculiar, together with the extent to which
they appear on the upper surface. The fore wing is especially
remarkable in these respects. The species is almost certainly
new and both striking and distinct; but the specimens are
unfortunately in such poor condition that it 1s impossible to
make either of them types. As the locality and time of year
are precise, it is to be hoped that some naturalist in Brazil
will capture examples which may be described, and named
after the great traveller and observer.
Westwood’s list agrees.
Euptychia electra, Butl.
Bz. 1306.4 8. 2. 29. 2=261 (Pl. VI. fig. 9, showing
underside) , 262 (fig. 10). Porto Real [Nacional]. “ Bo-
raciio.”
“This genus is entirely sylvan, and delights to hover
low among the herbage and thicker foliage. This was
collected by W. J. Burchell in Brazil. 365
caught in the Carasco, or thicker campo-woods ; and another
afterwards caught in the back yard.”
The two labels atfixed to each specimen are reproduced on
the Plate to the right side of the respective figures. The
lower number, written less carefully and with thicker lines,
is in each case an original Brazilian label. The upper number
and date, written by Burchell after his return, are upon a
separate piece of paper, although the overlapping upper edge
of the older label is in each case invisible.
Bz. 10. 2. 29. = 268, Porto Real [Nacional].
These three specimens were submitted to Dr. F. D. Godman,
who writes (Feb. 27, 1904) :—“ Your specimens, which
exactly resemble six I have from Chapada, have the four
ocelli on the hind margin of the underside of the fore wings
strongly marked, whereas in Butler’s type [of electra], which
is from Bahia, they are obsolete; but 1 have specimens
showing all intermediate gradations from Brazil. These ocelli
in the Satyride generally vary much both in size and distinct-
ness, and are not a very good character for distinguishing a
species.”
The ocelli mentioned by Dr. Godman are well seen in fig. 9
of the accompanying Plate VI.
Westwood’s list agrees.
Euptychia armilla, Butl.
8. 11. 28. 6= 264-269. Near Porto Real [Nacional].
“ Corrego Raiz.” Brazilian dates on 266, 268, and 269.
No data. = 270.
These specimens were kindly named for us by Dr. F. D.
Godman, F.R.S.
Agrees with Westwood’s list, except that the latter includes
a seventh individual captured 8. 11. 28, a second without
data, and an individual captured 10. 2. 29 (Porto Real).
Euptychia liturata, Butl.
26.9. 26. = 271. Santos. “Ina walk to the Chapel on
Montserrat.”
Bz. 30. 8. 28. = 272. Near Jaragua. “ Estiva.”
1250.+ 11. 9. 28. 2= 278, 274. Between Jaragua and
Cavalcanti. ‘“ Trahfras, R. Vendinha.” “ Papilio.
Flying low among grass in woods or margin of woods,
in considerable numbers. ‘They have the same habits
and hovering mode of flight as their congeners at the
Cape of Good Hope.” Brazilian label and later copy
on 274,
366 Miss Cora B. Sanders on the Rhopalocera
These specimens were also named for us by Dr. F. D.
Godman.
Westwood’s list probably agrees, except that an additional
ndividual captured 11. 9. 28 is mentioned. Another indi-
vidual, captured 26. 11. 26, is probably 297, accidentally
associated with /turata instead of camerta.
Euptychia acmenis, Hiibn.
10. 3. 26. 2= 275, 276. Riode Janeiro. Along the Carioca
Aqueduct.
18. 3. 26. 2= 277, 278. Rio de Janeiro. Along the Carioca
Aqueduct. Brazilian date on 278.
21.3. 26. = 279. Rio de Janeiro. Along the Carioca
Aqueduct.
3. 4. 26. = 280. Rio de Janeiro. Along the Carioca
Aqueduct.
Westwood’s list agrees.
Euptychia camerta, Cram.
Bz. 350. TI. 15. 10. 25. 2= 281, 282. Minas Gemes,
“ At the Discoberto do Antonio Velho; P[apilio].”
Bz. 470. I. 16. 10. 25. = 283. Minas Geraes. Discoberto.
“Papilio.”
Bz. 829. I.+ 23.10. 25. = 284. Minas Geraes. Disco-
berto. ‘‘Pap[eio}.”
O1g. 1.720, TO.” 200.22 = eoo, acco. Minas’ Geraes.
““ Plapilio]. At Discoberto, near Joiv Pedro’s house.”
Brazilian label and later copy on 285.
Bz. 1002. [.+ 27. 10. 25. = 287. Minas Geraes. ‘“ At
Sao Joao de Nepomucena and on the road from Discc-
berto. Papfilio].”
28. 10. 25. 2= 288, 289. Minas Geraes. (As 72.)
4.11. 25. 3= 290-292. 5 (As 19.)
Bz.+ 6.11. 25. = 2938. Minas Geraes. “At Capitao
Leite’s.”” Near Nepomucena.
9.2.26. = 294, Organ Mountains “By the River
Pacaqué.”
Bz. 17. 3.26. = 295. Rio de Janeiro. (As 216, 217.)
Bz. 20. 3. 26. = 296. 9 Along the Carioca
Aqueduct.
26. 11. 26. = 297. Santos. (As 8.)
7, 3. 27. 3= 298-300. Near S. Paulo. “ Morumby. Walk
to Porto.” “In Silva” on 299, ‘“Sylva” and date on
Brazilian label on 300.
collected by W. J. Burchell in Brazil. 367
21.3. 27. =801. Near §. Paulo. “On Road W. beyond
Prdea da Aleyria.”
8. 4. 27. =802. Near S. Paulo.
Sona ou A0e. ae
10. 5. 27. 2= 304, 305. Near 8. Paulo. About the Tiete
and near Sta. Anna.”
18. 6. 27. = 806. Near 8S. Paulo.
22. 3. 28. = 3807. Near Goyaz.
1. 4. 28. = 308. + :
19. 4. 28. = 309. ” ”
Bz. 30. 4. 28. = 3810. Near Goyaz.
Be, 12.6. 23... = 311. ”? ”
Bz. 1303. + 4. 2,29. = 312. Porto Real [Nacional].
“ Papilio. Caught in the back yard, and perhaps only
a weather-worn variety.”
5. 2. 29. = 3818. Porto Real [Nacional].
Bz. 6. 3. 29. = 314, Porto Real [ Nacional].
Ba. 9. BS 29. = 315. 9 ”
15: 3. rAe)8 = 316. 9? ”?
bz. + Whe ae 29: = 317. ”? 9
2555 OF 4294 fF 318. ” ”
22.4. 29. =319. Porto Real [Nacional]. ‘ Various”
[ ? places ].
z+ 19.5. 29. = 320. On R. Tocantins. R. Araguay.
202 do 29.) == de)... Re Tocantins, N., of Itaboca. Near
Falls of Guariba.
26. 6. 29. 2= 822, 323. Pard. “Near my house (Pomba
Rocinha).” Brazilian date and later copy on 823.
6.7. 29. = 324, Para.
Bloks 20.-— Ged. Bey
10. 9. 29: = 326, . Parad, S: José.
E710. 29... = SBT" 5, 3
8. 11. 29. 2= 328, 329. Pard, South of S. José.
fon it. 29. = 330, Pard, 5S, José; —‘ Caminho de: Cha-
monte,”
S. 12,29. = 331. Pard, 8. José. “Suburbane.”
Westwood’s list agrees in a remarkable manner with this
long series of specimens. He separated the individuals into
four sets (unnamed), apparently influenced by the develop-
ment of the eye-spots upon the underside. ‘The only differ-
ence is the substitution in his list of 22. 4. 23 for 22. 4. 29,
probably a mistake in copying, and the omission of 297.
The latter was probably included with the individuals of
liturata.
368 Miss Cora B. Sanders on the Rhopalocera
Euptychia quantius, Godt.
9.2.26. ¢ = 3832. Organ Mountains. “ By the River
Pacaqué.”’
This specimen has been submitted to Dr. F. D. Godman,
who considers that the species is probably quantius.
Westwood’s list agrees.
Euptychia renata, Cram.
27. 8. 28. g§ = 3833. Near Jaragua. Goiaveira. ‘ All these
Lepidoptera were caught at the ford of the rivulet at
Goiaveira, at 5 P.M.”
26. 5. 29. 9 = 834. OnR. Tocantins. (As 321.) “Silva.”
Westwood’s list agrees, except that 26. 8. 29 is substituted
for 26. 5. 29, probably a copyist’s error.
Euptychia marmorata, But).
Bz.+ 14. 2. 26. = 335. Organ Mountains. Near R. Pacaqué.
13. 4. 27. = 336. Near S. Paulo.
Bz. 10. 5. 27. =33%. Near 8. Paulo. “ About the Tiete
and near Sta. Anna.”
14. 6. 27. = 338. Near S. Paulo.
Westwood’s list agrees.
Euptyche libye.
31.5. 29. =839. R. Tocantins. Baifo. “P.[M.].”
17. 9. 29. = 340. Pard, 8. José.
17. 11. 29..2= 841, 342. =Paré, S: Jose.
7.1.30. = 348. Pard.
Westwood’s list agrees, except for an additional specimen
captured 10. 8. 29 (Pard).
Taygetis valentina, Cram., form euptychidia, But).
12. 5. 28. = 344. Goyaz. “Caught in the woodhouse.”
.. We owe this determination to the kindness of Mr. F. A.
Heron.
In Westwood’s list 15. 5. 28 is substituted for 12. 5. 28.
The words “ Caught in the woodhouse”’ are present, proving
that the discrepancy is merely a copyist’s error.
Taygetis Andromeda, Cram,
9. 3. 26. = 3845, Rio de Janeiro,
collected by W. J. Burchell in Brazil. 369
Bz. 10. 3. 26. = 346. Rio de Janeiro.
Bz, 1953: 26,344, “In the Valley
of Catombi.”
Westwood’s list agrees. 346 was separated as another
form.
Taygetis virgilia, Cram.
Bz. 197. I. 8. 9. 25. = 348, Rio de Janeiro. Along the
Aqueduct. “Papilio. Insylva; in crepusculo volitans.”
10, 3. 26. =349 (PI. VI. fig. 12; Burchell’s manuscript label
is reproduced below the figure). Rio de Janeiro.
Bz. 1054. Il. 17. 3. 26. = 850. Rio de Janeiro. (As
216, 217.) “ Both these Papiliones were caught in the
forest down the hill.” The Brazilian number and later
copy without date on 350.
1248.+ 7. 9. 28. 2= 351, 352 (fig. 11; Burchell’s reference
number and date are reproduced to the right of the
figure). Between Jaragua and Cavalcanti; near Rio
Maranhao. Fe Gudrda Mér. “ At twilight in deep
shady wood, where we slept this night. Has a hovering
motion and settles on the ground, P.M.” Brazilian
label and later copy on 361.
Westwood’s list agrees. He separated out 351, 352, evi-
dently on account of the character described below.
The Burchell specimens from Rio Maranhao (351 and 352)
show a rufous border on hind wing altogether absent from the
long series of this species in the Hope Collection. This
character becomes common in Central America. Thus we
read in the Rhopalocera of the ‘ Biologia Centrali-Americana ’
(vol. i. p. 97) :—“ The rufous margin, however, is more com-
monly seen in specimens from northern localities.” The
occurrence of the character in a pronounced form in both speci-
mens from a locality near the opposite end of the range of the
species may therefore indicate a local change or replacement
of form in seventy-five years. It is much to be hoped that a
traveller who has the opportunity of retraversing this part
of Burchell’s route may enable us to compare the two 1828
specimens with a good series from the same locality.
The striking ditterence as regards the hind marginal border
of the hind wings between 351, 352, and the specimens from
Rio (848-350) is well shown in figs. 11 and 12 on Plate VI.
Taygetis echo, Cram.
Bz. 16. 4. 28. = 353. Goyaz. “ Morro de Canta Gallo.’
“ In horto proprio.”
370 Miss Cora B. Sanders on the Rhopalocera
Compared with Godman-Salvin Coll. (6 L. Amazons,
1 N. Brazil, 1 no locality.) The Burchell specimen has a
broader brighter yellow band on fore wing than these, or six
Hope Coll. specimens (not Brazilian).
Westwood’s list agrees.
Pedaliodes phanias, Hew.
9, 2.26. ¢=354. Organ Mountains. “By the River
Pacaqueé.”
Westwood’s list agrees.
In addition to the individuals which Westwood’s list shows
to be missing from certain of the above-mentioned species,
three small categories separated out in the list have not been
traced at all. They are as follows :—
Hipparchia V. Two individuals—14. 6. 27 and 1399. 24.7.29.
ss XXVII. One individual—27. 8. 28.
5 XXXV. Four individuals—778. 15. 7. 25, one
without data, and the two following, which are
certainly erroneous: 737, shown by the note-
book to be a Cicada; 153, which is similarly
found to be a Cassida.
EXPLANATION OF PLATE VI.
The Plate has been printed from a half-tone block prepared from a
beautiful photograph of the actual specimens taken in the Oxford Univer-
sity Museum by Mr, Alfred Robinson. All the figures are the natural
S1ZC.
Fig. 1. Leucothyris phenomoe, Dbl. & Hew.,n. subsp. Burchell’. A repre-
sentation of specimen 64, the type of the subspecies. The heavier
black markings which are characteristic of Burchell’ as compared
with phenomoe are at once apparent when figs. | and 2 are con-
trasted with 3 and 4. Burchell’s label, written in England, is
reproduced to the right of the figure.
Fig. 2. Another example of the form shown in fig. 1. A representation
of 65. Burchell’s label, written in England, is reproduced to
the right of the figure.
Figs. 8 & 4. Two examples of Leucothyris phenomoe, Dbl. & Hew. Repre-
sentations of specimens 60 and 61 respectively. Burchell’s
labels, written in England, are reproduced to the right of the
figures to which they respectively refer.
Fig. 5. Dircenna dero, Hiibn. A representation of specimen 74. The
black markings are far less heavy than in figs. 6and 7. On the
collected by W. J. Burchell in Brazil. 371
other hand, it must be remembered that 74 isa male, while 68
and 72, the specimens represented in figs. 6 and 7, are females.
74 is also more worn than the other two, and this tends to
diminish the depth of the black markings. But, making all
allowances, 74 must always have been much less heavily
marked than 68 and 72. Burchell's label, written in England,
is reproduced to the right of the figure.
Fig. 6. Dircenna dero, Hiibn., form rhoéo, Feld. A representation of
specimen 68. H. W. Bates believed that this form is replaced
by typical dero in S.E. Brazil, and yet six out of Burchell’s
eight specimens from this very locality are rhoéo. Burchell’s
label, written in Brazil, is reproduced to the right of the figure.
Fig. 7. Dircenna dero, Hiibn., form rhoéo, Feld. A representation of
specimen 72, another heavily marked form, although the
median nervures of the hind wing are much less suffused with
black than in the specimen shown in fig. 6, which is peculiar in
this respect among all Burchell’s captures. Burchell’s label,
written in England, is reproduced to the right of the figure,
The figure appears to represent a butterfly with shorter broader
wings than those of the originals of figs.5 and 6. This is merely
the effect of fore-shortening, the wings of the former having
drooped after resetting. The obvious difference in the figures
is a convincing demonstration of the false impression of form
conveyed by the old British mode of setting with sloping wings.
Fig. 8. Euptychia sp. A representation of specimen 259. Burchell’s
label, written in England, is reproduced to the right of and
below the figure.
Fig, 9. Euptychia electra, Butl. A representation of the underside of
Fig. 10.
Fig. 11.
Fig. 12.
specimen 261. The four small submarginal ocelli on the fore
wing, which are so distinctly shown in the figure, are obsolete
in the type of electra, from Bahia. Burchell’s two labels are
reproduced to the right of and rather below the figure. The
lower number, which is really on a separate label, was written
in Brazil, the upper number and the date in England.
Euptychia electra, Butl. A representation of the upperside of
specimen 262. Burchell’s two labels are reproduced to the
right of the figure. They were written as described in fig. 9.
Taygetis virgilia, Cram. A representation of specimen 352.
The label, written by Burchell in England, is reproduced on the
right side. The rufous hind marginal border of the hind wings
is well indicated. This feature, which is characteristic of
Central-American specimens, is here found in both of Burchell’s
captures (7. 9. 28) trom the Maranhaio River, to the N.E. of
Goyaz.
Wagicta virgia, Cram. A representation of specimen 349.
The label, written by Burchell in England, is reproduced below
the figure. The pale brown border of the hind wings is seen to
be very different from that of fig. 11. The appearance here
shown is common to all three specimens from Rio (348-350),
just as that of fig. 11 is common to the two from the Rio
Maranhao.
372 Mr. W. F. Kirby—Notes on Phasmide
XLIT.—WNotes on Phasmida in the Collection of the British
Museum (Natural History), South Kensington, with Descrip-
tions of new Species.—No. 1. By W. F. Kirsy, F.L.S.,
THE Phasmide have been less studied than any other family
of Orthoptera, and the classification is still in a rather
unsatisfactory state. Many genera are at present somewhat
isolated, owing probably to the incompleteness of our collec-
tions, and many others include discordant sections which
require new names. Nor do we appear to possess sufficient
material to enable us to judge of the real value of even
such important characters tor defining natural groups as the
length and structure of the antennz and of the median cell,
and the presence or absence of the areole at the end of the
tibia beneath. I would suggest that the shape of the median
segment may perhaps be tound to be of great importance,
especially whether it 1s pointed, rounded, or truncated in front.
As I find myself unable to adopt Brunner von Wattenwyl’s
arrangement of 1893 in its entirety, I have drafted out the
following provisionalarrangementof subfamilies:—1. Loncho-
dine ; 2. Bacteriine; 3. Bacilline (including Bacillide and
Clitumnide of Brunner) ; 4. Diaphomerine ; 5. Bacteriine ;
6. Phryganistriine ; 7. Palophine ; 8. Necrosciine; 9. Acro-
phylline; 10. Eurycanthine; 11. Heteropteryginz ; 12. Ani-
somorphine; 13. Prisopine; 14, Pseudophasmine; 15. Aschi-
phasmine ; 16. Phylliinee.
Subfam. I. Lowcxoprvz,
Lonchodide, Brunner (pt.).
Includes Old-World species with long antenne and a short
median segment. Most of the genera are apterous, but one
or two (Oxyartes, Stal, for instance) have rudimentary wings.
Genus STZLONCHODES, Kirb., n. n.
Lonchodes, pt., Gray (nec sect. typ.) ; Stal (restr.).
Type, L. geniculatus, Gray.
‘lhis is Gray’s second species, but his own description
actually contradicts the characters of the genus Lonchodes ;
yet Stal has selected it as the type, an utterly unwarrantable
action. A considerable number of species may be tempo-
rarily included in Stelonchodes, but the genus will probably
be soon subdivided.
tn the British Museum. 373
Stelonchodes gracillimus, sp. n.
Long. corp. 100-116 mm.
Male.—Long and slender, rufous or rufous-brown, more or
less varied with blackish bronze or olive-green; antenne
bronzed ; head and pronotum rufous ; mesonotum, metanotum,
and median segment bronzy brown, except at their extre-
mities, which are rufous ; one specimen, however, is uniform
olive-green over nearly the whole of these parts; abdomen
either bronzy black, with tawny bands at the extremities of
the segments, or rufous as far as the sixth or seventh segment
and black beyond, with or without two white spots at the end
of segments 8 and 9; legs very long and slender, the middle
legs somewhat shorter than the others; all the femora
rufous nearly to the extremity; the rest of the legs bronzy
black above and somewhat paler below; middle and hind
femora finely serrated beneath towards the extremities, hind
femora extending beyond the base of the sixth segment of the
abdomen.
Hab. Tonkin (Than Moi), June and July (Fruhstorfer).
Allied to S. pragn and stomphax, Westw., but larger.
The very long and slender legs, with red femora, are very
characteristic,
Genus Loncuopes, Gray et auct.
Dexippus, Stal.
Gray’s description of this genus and of his first species,
L. longipes, clearly indicates that as the type.
Lonchodes (?) viridis, sp. n.
Female.—Bright green, with the following exceptions :—
antenne, except towards the base, a square spot at the extre-
mity of the first four segments of the abdomen (reckoning the
median segment as the first), and a dot on the sides of each
corresponding suture black or blackish ; and asalmon-coloured
streak on the sides of the meso- and metanotum, separated
below by a green line from a salmon-coloured line, bordered
below by a yellow one. Legs short, of nearly equal length ;
femora thick, straight, except for the usual curve at the base
of the front femora, and with a semicircular lobe at the
extremity of each lower carina, those on the front femora
small, those on the others conspicuous. First joint of front
tibize lobate above and nearly as long as the remaining joints,
Head and body unarmed, but with a fine carina running
374 Mr. W. F. Kirby—wNotes on Phasmide
- down the whole length, and thickly but finely granulated,
especially on the thoracic segments, which causes them to
appear very finely denticulated on the sides. Prothorax with
a raised carina in front and a central transverse sulcus.
Abdominal segments 2-7 at least twice as long as broad,
the eighth to tenth strongly carinated, the ninth shortest
and transverse, the others only slightly longer than broad ;
the tenth indented in the middle, to expose the small but
strongly carinated eleventh ; operculum boat-shaped, strongly
carinated on its hinder half, and not excavated at the extre-
mity, which extends as far as the tenth segment.
Hab. Tonkin (Than Moi), June and July (Fruhstorfer).
Described from two specimens.
This interesting species will probably become the type of a
new genus when the Lonchodine are revised.
Dimensions.
mm,
TIONP CONPOTISi ss dines Sets nee eles als 105-118
ne CADIS eis ieio ao, aioe ae etal aya 7
git cPROIOU ee ctr tat ickeks ceeletn ates ;
py MILER ONOEU ireia) siete ¢ cide tials otela 19-21
» metanoti, cum segm. med... 18-19
pe) AMON QIUG 1 fos iat ele tarts selene haere 19-20
i Fe ics hears A eh 14-16
5 Spy ePOSUsre aiola tem insnetale ahs aia 17-19
Genus OxYARTES, Stal.
Oxyartes lamellatus, sp. n.
Male.—Rather slender, brown; head with six tubercles on
the hinder edge; antennze pubescent, greenish brown, darker
towards the ends of the joints, nearly as long as the body,
and composed of about sixty joints, irregularly longer and
shorter ; pronotum with two erect spines near together in
front, and two longer ones (wider apart) behind the first lobe ;
mesonotum smooth, inclining to greenish, with a pair of strong
spines near together in front and five pairs behind (one pair on
each side of the median line, one pair in front of these, sepa-
rated by the median line, and one pair on each side before the
base of the almost obsolete tegulz), there is also a lateral row
of shorter spines, followed by a lower row of tubercles; meta-
notum with two spines between the bases of the wings and
three larger ones on the metapleura ; wings black, paler at
the base and on the costa, narrowly oval, and extending as
far as the middle of the median segment; meso- and meta-
pectus studded with black tubercles, a distinct tubercle on the
in the British Museum. 375
median line above towards the extremity of each abdominal
segment. Legs pubescent, carinated; femora with two or
three small teeth on each side beneath before the extremity.
Female.—Larger and stouter than the male and darker
brown, but inclining to grey on the head, pronotum, antenne,
and legs; antennze spotted with brown on most of the joints;
head with four short and broad tubercles on the hinder edge,
two central and two lateral ; mesonotum rugose, covered with
tubercles and laterally with short spines, continued on the
meso- and metapleura; mesonotum with two strong spines
near the middle in front, the left-hand one with a smaller
spine adjoining it; there are also two strong spines, wider
apart, towards the hinder extremity, and at the hinder edge
itself three or four close together on each side; metanotum
and abdomen rugose and more or less granulated, two short
spines on the latter between the wings, which are blackish
and broader than in the male; abdomen with a short tooth
near the extremity of each segment in the median line, and
from the sixth segment to the extremity strongly carinated,
the carina on the seventh segment rising into a large lamella
for the greater part of the segment, preceded by a smaller
one on the sixth.
Hab, Tonkin (Than Moi), June and July (Fruhstorfer).
Described from one male and two females.
Allied to O. despectus, Westw., but larger, and with stronger
and differently arranged spines.
Dimensions,
é. Q.
mm, mm.
PONE RUHL POTISL a aeiacie gee a aeroian as 84 102-125
jj) CAPA: Sirod. Ciena owes « 8 7-9
sf Luprenosbi, Sol ienasscin dusts leat 5 7-9
gE IMGROHOEE Gta xictoys ¢ «jv gt ece fon: LO 20-29
* 4, metanoti, cum segm.med..... 11 13-15
fp CIM RINE SB clers ure eae a talqel ate 6 8-9
Fpieg etihe, ATM 5 clap ata: a o/s bute Sh Mere 25 21-25
ie ps peeks YR cls wid i sees 19 18-21
2 rae) (GLP sre Cort ari Cone 3l 21-25
BEAU Ce A TSA CCE Te 16 8-9
EE eto ca cop heysielaay wes 3 0 2s Eee = 3-
Genus PRoMACHUS, Stal.
Promachus (?) letus, sp. n.
Apora leta, Brunner, MS.
Long. corp. 65-82 mm,
Male.—Green ; rather slender, front and hind legs of
376 Notes on Phasmidve in the British Museum.
nearly equal length, the latter extending nearly to the extre-
mity of the fifth segment of the abdomen; middle legs
shorter than the others. Face varied with whitish, and base
of the antenne shading from green into blue. Pronotum
with a transverse sulcus just before the middle; mesonotum
with four or five large asymmetrical black spines, thickened
at the base, and with a row of concolorous denticulations on
the sides, followed by a black spine before the base of the
four hinder legs ; hind femora slightly denticulated beneath
at the extremity; median segment about two fifths of the
length of the metanotum, rounded in front; segments 2-6 of
the abdomen with a small terminal tooth on the median line;
all the segments of the abdomen longer than broad, except
the tenth, which is carinated, but scarcely indented at the tip;
operculum boat-shaped, scarcely longer than the ninth
segment; cerci short, stout, slightly incurved.
Female (long. corp. 110 mm.).—Bright green; rather
stout, but tapering towards both the head and tail ; a brownish
line running along the lateral borders of the thorax and
abdomen; mesonotum with some small scattered black
tubercles, or, rather, granules ; meso- and metapleure spinose
on the dark lateral line already referred to; abdomen with
some more or less complete double carinations on the median
line of the hinder segment, and with a single slightly undu-
Jating carina on each side; there is a small tubercle or spine
at the end of the first seven segments, including the median
segment ; on segments 2-7 stand two or three green tubercles
above the lateral line; the tenth segment is twice suddenly
contracted at the sides and terminates in an obtuse triangle
above; the double median carina on the ninth coalesces into
a single steep carina, which continues to the extremity of the
tenth ; operculum pointed and channelled, extending beyond
the tenth segment to more than twice the length of the latter.
Hab. ‘Tonkin (Matton Mountains, 2000-3000 metres),
April and May (Fruhstorfer).
The male of this species is closely allied to P. Wallacet,
Westw., from Aru, the type of the genus, but is easily distin-
guished by the spineless head and the black spines on the
mesonotum. ‘The female, however, like that of the following
species, wants the long, projecting, spear-like process above
the operculum, so conspicuous in that of P. Wallacet. ‘The
specimens were received under the MS. name of Apora lata,
Brunn. ‘The specific name I have of course retained, but
the generic name is preoccupied in Polyzoa, and is therefore
inadmissible,
On the Genus Ortmannia, Rathd, - 377
Promachus (?) bicolor, sp. n.
Long. corp. 55-57 mm.
Male.—Rufous ; the antenne, spines, a broad band down
the middle of the body, bisected by the rufous carina, an
interrupted lateral line, and the legs beyond the apical fourth
of the femora black or blackish. Head with two pairs of
spines near the back ; pronotum deeply sulcated before the
middle, with a pair of long spines on the front lobe and small
lateral ones at the front angles, and two pairs of spines (the
first longest) on the second lobe. Mesonotum with five pairs
of spines (the last pair approximating) on the central region,
and a row of six spines on each side on the lateral black line ;
metanotum, median segment, and several of the basal seg-
ments of the abdomen with a pair of central spines, diminish-
ing in size hindwards; there are also two strong lateral spines
on the metanotum and two on the meso- and metapleure,
Segments of the abdomen hardly twice as long as broad;
hind legs rather Jonger than the others, extending as far as
the extremity of the seventh segment of the abdomen.
Female (?).—Larger and stouter ; testaceous, mottled with
blackish; the spines arranged nearly as in the male; legs
shorter, stouter, and carinated ; hind femora extending rather
beyond the fifth segment of the abdomen; abdomen with a
sinuous carina on the sides of the segments, segment 10
tripartite at the extremity ; except the front lobe of the pro-
notum, the whole median line of the thorax and abdomen is
traversed by a very strong raised carina. Abdomen without
terminal spine; operculum not projecting beyond the last
segment.
Hab. Tonkin (Than Moi), June and July (Fruhstorfer).
XLIII.—On the Genus Ortmannia, Lathb., and the Mutations
of certain Atyids. By EK. L. Bouvier *.
THE shrimps of the family Atyide belong exclusively to
fresh water. Despite their adaptation to this special medium
and the strange aspect of their most typical forms, they
attach themselves by a series of genera to the most primi-
tive of the marine shrimps. From Xtphocaris, of which the
cheles are normal and are furnished with exopodites on all
the feet, one passes to Atyephyra, in which the exopodites
have disappeared on the three posterior pairs of feet, to
Caridina, which have no expodites and whose anterior
* Translated from the ‘Comptes Rendus,’ t. exxxviii. p. 446,
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 25
378 M.E. L. Bouvier on the Genus Ortmannia, Rathb.,
chele are alone modified, then to Ortmannia, M. Rathbun
(Atyotda, Ortmann), in which the modifications take place
in the chelz of the first two pairs of feet, and at last one
comes to the terminal forms of the family, the Atye, of which
the very curious chelz are split right down to the base and in
consequence are devoid of a palmar region. Further, in the
genus Atya itsclf it is possible to establish a series of species
which progressively depart from Ortmannia. By its small size
and its rostrum, subtriangular and toothed below, A. serrata
presents some resemblance to Ortmannia mexicana, Sauss.
(O. potimirim, F. Miiller), whilst A. gabonensis, Giebel,
A. robusta, A. Milne-Edwards, and many other forms stand
out at first sight by their very marked adaptive characters :
large size, rostrum laterally serrated, feet of the third pair
sincularly strong and robust, &c.
It appears that Ortmannia is separated from all species
of Atya by two very constant characters: on the one
hand, the form of the chele, which are normal, with a
relatively short mobile digit and a well-differentiated palmar
region; on the other, the development of the carpus, which
is longer than wide, at least in the feet of the second pair.
These two characters are of the first importance; they
bring tcgether Ortmannia, Caridina, and Atyephyra, whilst
they separate them considerably from the Atye.
In studying the Atyide in the collection of the Museum,
a batch of shrimps, collected at Honolulu by M. Ballieu,
particularly attracted my attention. These shrimps were
Atyidee of small size, all adult, and in other respects very
much alike; but some presented all the characters of Atya
bisulcata, Sp. Bate, whilst others belonged very clearly to
the genus Ortmannia.
In 1901, Miss Mary Rathbun made an analogous observa-
tion on the Atyide collected on the Sandwich Islands by
Mr. Henshaw; she grouped in the species of Sp. Bate all
the examples with short carpi and chelz split down to the
base ; the others she regarded as types of a new Ortmannia,
O. Henshawt. I found myself confronted by the same
forms, but I was led to regard them quite differently from
Miss Rathbun.
Setting aside the generic characters affecting the carpi and
chelee, these two forms resemble one another in all respects :
same structure of rostrum, antennze, buccal appendages, same
tegumentary ornaments, everywhere the most absolute
identity—somewhat strange in species belonging to different
generic types. More than this, the two forms have that
similarity of appearance which characterizes all the repre-
sentatives of a single species, and which, in the deter-
and the Mutations of certain Atyids. 379
mination of species, is a more rapid and sometimes a surer
guide than the examination of morphological characters.
In my opinion, Ortmannia Henshaw? is neither more nor
less than a form of Atya bisulcata, a form which has
the curious character of recalling the immediate ancestral
form of Atya. We have not here to deal with an ordinary
dimorphism, sexual, produced by season or locality: the
specimens of M. Ballieu were collected in the month of May,
1877, in the vicinity of Honolulu, perhaps with one stroke of
the net; in both forms there are the same variations of size
and sex. Some females of Atya bisulcata are charged with
ova, whilst the females of the Henshaw? variation have none;
but in another consignment, also made by M. Ballieu, the
females of this variation carry a remarkably large charge
of ova.
I should not perhaps have hazarded the foregoing con-
clusion if the Museum material had not permitted me to
extend it to other quarters of the globe.
In 1890, M. Alluaud collected in a torrent on the Amber
Mountain, in Madagascar, a small shrimp which presented
all the characters of the genus Ortmannia, but differed from
the modification Henshawi by specific characters; latterly
the Museum has received from Sainte Marie, in Madagascar,
a small batch of shrimps *, in which examples of Atya and
Ortmannia absolutely resembling one another (setting aside
generic characters) were mixed. ‘lhe specimens of the first
form appeared to me to be classifiable as Atya serrata,
Sp. Bate: those of the second resembled that from the
Amber Mountain; they have all the specific characters of
Atya serrata, and represent certainly, in my opinion, a modifi-
cation of this species. ‘This will be, if desired, the modification
Alluaudi of A. serrata.
A. serrata exists also in the island of Bourbon, where
Maillard, about 1854, obtained three specimens, which are
now in the Museum. ‘The modification Alluaudi of this
species was found, in 1893, by M. Alluaud in the ravines of
the mountains of Salasie and Helbour. Another specimen
was taken by M. Alluaud, in 1890, in Mauritius ; the typical
A. serrata has not yet been noted in this island, but one
cannot doubt its existence there as well as in Réunion.
These modifications are of great interest, because they put
in evidence one of the mechanisms by which new types are
produced and definitely established through more primitive
types which may persist or disappear.
* These shrimps were captured in a little rivulet near Sainte Marie
in October 1895, and were presented to the Museum by M. Edouard
Cheyreux,
25*
380 On the Genus Ortmannia, Rathd.
In face of these modifications, one cannot doubt but that the
Atye are the direct descendants of Orimannia, and that, in the
case of certain species, this derivation is not yet a definitely
accomplished fact. It is naturally among the small forms,
nearer than any others to the primitive Atyide, that this
condition of unstable equilibrium is seen still to exist, in
which the same creature may indifferently present the form
of the past or of the future: Atya bisulcata and Atya serrata
are still in this stage. In Ortmannia americana the
primitive form alone exists; either it has persisted after
having produced the Aya, or it isin a state of evolution
towards the production of this kind, which is more probable.
In Atya brevifrons, de Man, on the contrary, the primitive
form seems to have disappeared, bequeathing a very marked
stamp to its descendant, which is small like the Ortmannia
and provided as it is with locomotor feet of small power.
A, brevifrons is a common species in the islands of the
Pacific; it has never been noticed under the form Ortmannia,
but it is possible that in some island it persists still in that
state.
It goes without saying that in the most typical Atye
(A. robusta, A. scabra, &c.), which are greatly modified and
of large size, one would not expect to find specimens having
the Ortmannia form.
Here, then, manifestly are mutations by atavsm which
show us how new types are formed and old types persist.
Actually, Atya bisu/cata and A. serrata are represented by
individuals of two kinds—the one with chele split down to
the base, the other with normal chele. If these species were
social, the individuals of each type might be called upon to
play a different réle in the colony, and to a certainty the
characters which distinguish them would go on exaggerating
themselves in consequence.
May we not explain in the same way the mysterious
presence of polymorphic individuals in the societies of ants
and termites? and the starting-point of the polymorphism
of these forms, would it not be an atavic mutation similar
to that of the Atye?
] return to the domain of pure systematics. The genus
Ortmannia should persist, but it comprises up to the present
time, it appears, only a single independent species— OV. meai-
cana, of Tropical America. The modification Henshawi of
Atya bisulcata and the modification Alluaudi of Atya serrata
are clearly Ortmannia; but they represent species in course of
evolution, which, according to circumstances, may persist or
disappear as Ortmannia; it is useful to look upon them no
longer as independent species, but as the atavic form of the
On a new Species of Acis. 381
species of Atya which issued from it. It is easy to verify upon
the spot the exactness of the views expressed in this note.
Those who do not accept them may always regard the two modi-
fications described above as distinct species of Ortmannia *.
XLIV.—Notes on a new Species of Acis. By W. D.
Henperson, M.A., B.Sc., Zoological Laboratory, the
University, Aberdeen.
WuiteE working along with Prof. J. Arthur Thomson over a
collection of Indian-Ocean Alcyonarians I recognized the new
species here described. It was included in a collection made
by Prof. W. A. Herdman in Ceylon.
The colony is large and fan-shaped, rising to a height of
149 mm. and having a maximum width of 167 mm.
From a conical base, which has a flat spreading margin and
is attached to a mass of worm-tubes, the short main stem
arises. At a distance of 14 mm. from its origin, where it
has a diameter of 3°5 mm., it divides into two principal
branches.
The branching is for the most part confined to one plane,
but several of the smaller branches and twigs arise at right
angles to the principal plane of branching. The branching
is very profuse and at several points shows anastomosis of
the branches, but this is by nomeanscommon. The branches
are cylindrical, but there are traces of slight flattening in the
plane of branching. ‘The twigs arise usually at right angles
to the branches, and their tips as well as those of the branches
are slightly clavate.
The polyps are small and are scattered over the whole
surface of the stem and branches. In no place can it be said
that they are confined to three surfaces, nor can any attempt
at lateral arrangement be seen. ‘The verruces are very small
and the polyps can be completely retracted within them.
The edges of the verruce show a variable number of spines
which project above the slightly conical operculum formed by
the tentacular spicules when the polyps are withdrawn.
The superficial coenenchyma of the stem and the branches
presents a striking appearance, due to the arrangement of the
large flat whitish spicules and to their being outlined against
the darker ground-colour of the stem and branches.
The spicules of the general coenenchyma are flat and multi-
tuberculate, varying very much in size and shape. The
* M. Ortmann regards Atya bisuleata, Spence Bate, as an Ortmannia
(Atyorda), although the examples studied by the English author had the
true Atyan chele ; I may add that M. Ortmann does not appear to have
observed the curious variations of this species,
382 Mr. O. Thomas on a
tubercles are low and rough and very numerous. Many of
the Jarger spicules extend the whole distance between two
adjacent polyps, and sometimes even exceed this length. They
fall into three groups, fairly distinct in shape :—(a) large
modified fusiform spicules, which taper more or less towards
the ends and measure from ‘9-3 mm. in length by *25—45 mm.
in breadth ; () squamous or scale-like spicules, often with
slightly lobed margins, which measure from ‘8-l‘1 mm. in
length by ‘4-6 mm. in breadth; and (ec) large modified
squamous spicules, consisting of a flattened tuberculate basal
portion and of a projecting part which forms the projecting
spine of the verruce. They measure, in length by breadth
in millimetres, as follows:—'7 x ‘5, °6x ‘4, ‘5 X°3.
In the polyps there are slender spindle-shaped and club-
shaped spicules. They are often slightly curved and either
taper to both ends or are blunt and rounded at one end and
pointed at the other. Many of these exhibit fairly prominent
spines towards the thicker end. They vary considerably in
size, being from *3—-"5 mm. in length and from ‘02-06 mm.
in breadth. They are found chiefly in the tentacles, where
they form an operculum to the retracted polyp; but an incom-
plete and irregular crown or collar is formed by them at the
base of the tentacles.
In colour the spicules vary from white to semitransparent,
while the whole colony has a whitish-brown appearance.
This species differs from Acts pustulata in not having
violet-coloured opercular spicules and in the branches not
being compressed in the plane of branching. It also differs
from Acis ortentalis in having the polyps on all sides of the
stem and branches and in the branching not being confined
to one plane.
From the fact that it was collected in Ceylon waters I
propose to name it Acis ¢ndica, to mark it as distinct from
Acis orientalis.
Hab. Deep water off Galle, Ceylon.
XLV.—A new Bat from the United States, representing the
European Myotis (Leuconoe) Daubentoni. By OLDFIELD
‘THOMAS.
THE subgenus Leuconoe* has not been hitherto recognized
as occurring in North America, but Myotes yumanensis should
probably be regarded as a member of the group, although
not a strongly marked example of it.
* Type, Myotis Daubentoni, the “ Wasser-Fledermaus.”
new Bat from the United States. 383
Now, however, I am able to record that Leuconoe in its
most typical form does occur in that continent; for Mr. J.
ffolliott Darling, a naturalist already known to zoologists for
his work in Mashonaland, has recently presented to the
British Museum a bat, obtained in the Yellowstone Park,
which is evidently closely allied to the typical species of the
subgenus, M. Daubentoni.
Thanks to the kindness and generosity of the authorities of
the United States National Museum, [ have had for com-
parison with Mr. Darling’s bat a complete series of North-
American Myotis, as worked out in Mr. G. S. Miller’s fine
monograph of the group. None of the bats there described
can be confused with it, nor have any species been described
since.
It may be called
Myotis (Leuconoe) carissima, sp. n.
Closely allied to the European M. Daubentoni, which it
evidently represents in North America.
General characters and proportions as in Daubentont.
Sides of muzzle heavily whiskered. Ears narrow, of medium
length ; laid forward in the spirit-specimen they just reach
to the tip of the nostrils; their inner margin evenly convex
below, slightly concave before the tip, which is narrowly
rounded off; outer margin excavated above, slightly convex
below; basal lobe well marked, rounded. Tragus rather
short, with straight inner margin, narrowly rounded tip,
sloping outer margin, and well-defined basal lobe.
Feet very large, their length more than two thirds that of
the tibia; claws medium.
Wings attached to the side of the metatarsus. Calcars
very long, more than double the length of the free portion of
the uropatagium, their tips forming prominent lobules exactly
as in Daubentont; no postcalcareal lobules. Tail scarcel
projecting from membrane. Wings hairy for about half an
inch on each side of the body, above and below; base of
uropatagium thinly haired, its free edge quite without fringe.
‘Toes with tufts of hair overhanging the claws.
Colour above and below (in spirit) uniformly smoky
blackish, the tips of the hairs indistinctly buffy or pale
brown. Ears, wing-membranes, and feet also blackish.
Anterior premolar about twice the size of the second,
decidedly drawn inwards, but in older specimens it might
take its place in the general line.
Dimensions of the type (measured on the spirit-specimen) :—
Forearm 88 mm.
Head and body 45; tail 86; head 17; ear 138; tragus
384 Mr. O. Thomas on Three new Bats.
on inner edge 5:5; thumb 8; third finger, metacarpus 33,
first phalanx 11°5, second phalanx 10°5, third phalanx 7°? ;
fifth finger, metacarpus 31, first phalanx 9, second phalanx 9;
tibia 16; hind foot (ec. u.) 11; calcar 16; free border of
uropatagium 6.
Hab. Yellowstone Lake, Yellowstone Park, N.W.
Wyoming. Alt. 8000 feet.
Type. Female (just adult). B.M. no. 4. 4. 25. 1. Col-
lected September 1903; presented by J. ffolliott Darling, Esq.
“ Caught flying about the Lake Hotel, although the weather
was snowy.”
This bat is very closely allied to M, Daubentoni, but has
a more strongly whiskered muzzle, rather larger ears, a less
projecting tail-tip, and appears to be darker in colour
throughout.
My own inclination would still, however, be to regard it
as a subspecies of M. Daubentoni; but as I am not writing a
eneral monograph of the group, it seems better in the case
of a United States bat to conform to the ideas about nomen-
clature prevalent in that country.
From M. yumanensis saturatus, Miller, apparently its
nearest American ally, J/. carissima is readily distinguishable
by its much longer forearm and still larger feet. AZ. sub-
ulatus, Say, of similar size, has conspicuously smaller feet
and broader ears.
The British Museum also contains another bat, from Lake
Winnipeg, collected by Sir John Richardson, which appears
to be referable to MZ. cartssima, but is unfortunately im too
bad a condition for certain determination. It was referred by
Dobson to M. lucifugus, but is certainly not that species.
Allowing for the great altitude of Lake Yellowstone, the
occurrence of the same species at Lake Winnipeg, considerably
further north, would be quite natural.
In the Old World M. Daubentoni occurs in Scandinavia,
and, as Dobson says, “attains the most northerly range of
all the species of the genus.”
XLVI.—Three new Bats, African and Asiatic.
By OLDFIELD THOMAS.
Hipposideros Commersoni and its subspecies.
The bats currently referred to H. Commersoni fall into four
groups, divisible by size, by the number of supplementary
nose-leaves, and by colour.
Mr. O. Thomas on Three new Bats. 385
The common mainland form is the largest, with a forearm
measurement of 95 mm. and upwards, and with the lower
tooth-row (front of canine to back of m3) about 15 mm. It
has four well-developed supplementary leaflets, and often the
rudiment of a fifth. In coloration it has the brown and white
markings described by Peters well defined and distinct, except
in such individuals as have the reddish suffusion so often
found in members of this genus.
Its synonymy appears to be as follows :—
Hipposideros Commersoni gigas, Waen.
Rhinolophus gigas, Wagn. Syn. Phyllorhina vittata, Peters, and
Phyllorhina Commersoni, var. marungensis, Noack.
In Madagascar the typical H. Commersoni, Geoff., is found:
small (forearm about 80-90 mm. ; lower tooth-row about 13) ;
supplementary leaflets three, the rudiment of a fourth being
occasionally present ; coloration dull greyish, with but little
indication of the characteristic dark dorsal markings.
In the island of San Thomé, on the opposite side of Africa,
is found a somewhat similar form, H. Commersoni thomensis,
Bocage, which agrees with true Commerson? in essential
characters, but is even darker, and has a prominent whitish
spot on each shoulder at the insertion of the antebrachial
membrane.
Finally, in British East Africa and Zanzibar there occurs
a form agreeing with Commersoni and thomensis in size, but
with the four leaflets of gigas and well-defined colour-
markings. It may be briefly diagnosed as follows :—
fipposideros Commersoni mostellum, subsp. n.
Size small, as in Commerson?. Supplementary leaflets
four, with rudiment of a fifth. General colour whitish, the
brown Y-shaped marking of the back well defined ; under
surface creamy whitish, a brown line across each shoulder
separating off a white patch at the insertion of the ante-
brachial membranes.
Skull and teeth as in true Commersoni, the cheek-teeth
conspicuously smaller than in gigas.
Dimensions of the type (measured in skin) :—
Forearm 92 mm.
Skull: length from cingulum of canine to back of occipital
crest 82; basal length to cingulum of canine 26:5; zygo-
matic breadth 18; mastoid breadth 15; upper cheek-teeth,
front of p* to back of m* 8-4; front of lower canine to back of
Mz 13.
386 Mr. O. Thomas on Three new Bats.
Hab. (of type). Tana R., British East Africa. Other
specimens from Zanzibar.
Type. Male. B.M. no. 89. 3.8.3. Presented by H.C. V.
Hunter, Esq.
Rhinolophus Denti, sp. n.
Allied to the European &. euryale, but smaller.
Size very small, among the smallest species of the genus.
Leading characters (in the order used in Dobson’s synopsis) :
posterior upper premolar separated from the canine, though
not very widely, the small anterior premolar in the tooth-row,
towards its outer side; horizontal portion of the sella not
widely expanded, though (allowing for shrinkage in the dried
skin) it would appear to be more so than is usual in the
allied species; upper margin of the posterior connecting
process forming a marked projection, rounded terminally,
rising considerably above the summit of the front of the sella ;
sides of the vertical process of the sella parallel, summit
broadly rounded off ; antitragal notch shallow.
Horseshoe large, covering most of the muzzle, circular, its
anterior edge sharply notched in the centre; lancet short,
conical, its sides evenly convergent upwards, thickly covered
with fine fur, similar in colour and quality to that of the head.
Ears of medium size, their inner margin evenly convex, tip
sharply pointed, upper half of outer margin slightly concave ;
antitragal notch not deep and the lobe itself comparatively
little convex. Hind limbs slender and delicate. Wings from
the lower third of the tibia. Interfemoral membrane finely
fringed posteriorly.
Fur close and fine, about 7 mm. long on the back. General
colour above pale grey, the individual hairs dull whitish, with
dark brown tips. Under surface nearly white. Membranes
brown, the plagiopatagium and interfemoral inconspicuously
edged with white.
Skull with the nasal convexity more developed than in
R. euryale, less than is figured in Peters’s R&. lobatus*.
Palate ending opposite the posterior edge of the internal lobe
of m?.
Dimensions of the type (those in inverted commas taken
by the collector in the flesh) :—
Forearm 42 mm.
‘“‘ Head and body 41”; ‘tail 21”; “ear 20”; nose-leaf
(dry) 9°2x6°3; lower leg and foot (c. u.) 25°9.
* Reise Mossamb., Saug. pl. xiii. fig. 17.
Mr. @. Thomas on Three new Bats. 387
Skull: greatest length 17; basal length to front of canines
13:2; breadth of brain-case 7°6 ; palatal bridge 1:9; front of
upper canine to back of m* 5:9; front of lower canine to back
of Ms 6°6.
Tab. Kuruman, Bechuanaland. Alt. 1300 m.
Type. Male. B.M. no. 4. 4. 8. 2. Original number 7.
Collected 24th January, 1904, by R. EK. Dent. Two
specimens.
“ Caught in a house.”
This species, the smallest of South-African Rhinolophz,
seems to represent ft. euryale, but may be readily distin-
guished from that, as from all others, by its proportions, its
pale colour, the high attachment of its wing-membranes, and
its unusually hairy lancet.
Pipistrellus raptor, sp. n.
A rather large species, with long head, proportionally short
forearms and tibiz, and with a bone in the very large penis.
Size rather large, form clumsy. Head long, half the length
of the forearm, almost equally broad in front and behind.
Muzzle swollen, smooth and rounded ; the nostrils small, their
edges not projecting ; middle line above more deeply grooved
between the glands. Lars rather small; base of inner edge
with a very narrow hem ; inner margin straight, tip narrowly
rounded off, outer margin evenly but slightly convex to the
shallow emargination separating the low basal lobule. Tragus
short, broad, broadest opposite the lower third of the inner
edge, the latter straight or slightly concave, tip rounded,
outer margin evenly convex, basal lobule distinct, triangular.
Wings to the base of the toes. Hind limbs short, feet stout
and heavy. Calcar reaching about halfway towards the tip
of the tail, its end marked with a projecting lobule; post-
calcareal lobe short, but very broad and distinct, supported
by a well-marked supplementary cartilage. Tail rather
short, of seven vertebree and a terminal rudiment, involved
in the membrane practically to its tip. Penis enormous, as
long as or longer than the tibia, the development being
mainly in the lengthening of the glans (which is slender and
contains a long os penis) and the prepuce; the latter is club-
shaped, well-haired, grooved above terminally.
Fur extending on to the wing-membranes for about one
third of an inch on each side of the body and for a similar
distance on the interfemoral; below, a slightly wider area is
hairy. Scattered hairs present on ears, the external basal
lobe thickly hairy externally.
388 Mr. G. E. H. Barrett-Hamilton on some
General colour above dark bistre brown, the ends of the
hairs prominently lighter, buffy brown. Below, similar but
lighter. Hinder aspect of pubis buffy to base of hairs.
Skull long and low, with a very deep nasal notch. Teeth
on the whole like those of P. ceylonicus (P. indicus, Dobs.).
Inner incisors long, their secondary cusp well developed,
postero-external ; outer incisors just equalling in length the
secondary cusp on the inner ones and with an indistinct, low,
postero-internal, basal cusp, and a posterior hollow for the
tips of the lower canines, as in P. ceylonicus. Large pre-
molar close to back of canine; the well-developed small pre-
molar visible with difficulty from without. Lower incisors
slender, scarcely overlapping. Lower canines with a broad
cingulum, making its section circular. Anterior lower pre-
molar three fourths the height of the second.
Dimensions of the type (measured in spirit) :—
Foream 37 mm. (range 36-39).
Head and body 51; tail 86; head 18; ear 13:5; third
finger 65; tibia 12; hind foot (c.u.) 9; penis 15, its terminal
portion (with the bone) 11.
Skull: greatest length 14:5; upper length in middle line
12; basal length in middle line 10°9; zygomatic breadth 10°6;
interorbital breadth 6:1; constriction 4; mastoid breadth 8°6 ;
length of brain-case 5:7; front of canine to back of m* 6 ;
front of lower canine to back of m3 6°1.
Hab. Tonkin.
Type. Adult male in British Museum. Collected by
Mr. H. Fruhstorfer. Six specimens examined.
This species may be readily distinguished from all its allies
by the enormous size of the penis and the presence of a bone
in that organ. From Dobson’s “ Vesperugo affinis,” only
known from a female, it may be separated by its shorter and
fewer-jointed tail, stouter feet, shorter tibia, and other
characters. P. brachypterus, Temm., of which I have not
seen a specimen, has shorter outer incisors and the wing-
membrane arises from the tarsus; described originally from
an old male in spirit, no mention is made of the penis.
XLVII.—Notes and Descriptions of some new Species and
Subspecies of Mustelide. By G. E. H. BArRerr-HAMILTON.
In working through the Mustelide in the British Museum of
Natural History | find several forms which seem to me to be
worthy of recognition mainly because they are either distin-
gishable as local races of well-known species, or, as in the
new Species and Subspecies of Mustelidee. 389
case of the Greenland stoat, are sufficiently differentiated to
claim a title to full specific rank.
Firstly, as regards the pine-marten, I find a tendency to
deeper coloration and a brighter throat-patch in the southern
representatives of the species. I propose for these the sub-
specific name Mustela martes latinorum, and I take as type of
the subspecies a male (no. 95. 4. 16. 1) from the Nurri
Mountains, Sardinia, presented by Mr. EK. N. Buxton.
In this specimen the general colour is between “ seal-
brown” * or “ mummy-brown,” darkest on the tail, limbs,
and, to a less degree, the central dorsal region. The
yellowish- brown underfur, yellower than in British martens,
frequently shows through the long outer hairs. The ears are
edged and faced with dirty brownish-white hairs, The exten-
sive throat-patch is rich “ orange-buff,’ deepest near its °
centre. It reaches from the “ interramia”’ t, where it sends
forward a small central projection, to slightly behind the
region of attachment of the fore limbs, near which it is
interrupted by one or two detached areas of the brown colour.
Its edges are sinuous.
No dimensions taken from the animal whilst in the flesh
accompany the specimen; but it was evidently an adult male,
having a hind foot and ear measuring 41 and 35 mm. respec-
tively in the dried skin.
The dimensions of the skull are :—Greatest length 90 mm. ;
basal length 84; palatal length 43; zygomatic breadth 51.
I have also examined examples of this form obtained by
Messrs. Oldfield Thomas and R. I. Pocock in Majorca and
Minorca.
Amongst the polecats, I find in the south a tendency to
assume yellow underfur and face-markings, while in Central
Europe the face-markings are more extensive, and both they
and the underfur are whiter.
As type of the former subspecies, which may be known as
Putorius putorius aureolus, I take no. 94. 3. 12. 1 (a female),
killed at Ferrol, Spain, on the 23rd of June, 1893, and
presented by Dr. V. L. Seoane.
The colour, above and below, is deep seal-brown, especially
dark upon the limbs and chest. The ears are edged with
dirty yellowish white, and the cheeks, upper lip, interramia,
and a band running up from the latter between the eye and
* Names of colours in inverted commas are from Mr, R, Ridgway’s
‘ Nomenclature of Colors, 1886. ¥
+ Ladopt this term from a suggestion of Mr. Oldfield Thomas.
390 Mr. G. EE. H. Barrett-Hamilton on some
ear on each side, but not extending to the crown of the head,
are of the same colour. ‘The underfur is yellowish buff.
The dimensions of the hind foot and ear, taken from the
dried skin, are 61°5 and 19 mm. respectively.
The dimensions of the skull are :—Greatest length 66 mm. ;
basal length 60; palatal length 31; zygomatic breadth 44.
The Central-European polecat, on the other hand, has a
nearly white underfur, and the long outer hairs are nearly
black. The facial markings also are nearly white and the
two bands between the eyes and ears are carried upwards
until they meet and form a V-shaped mark, with the blunt
point of the V lying on the forehead between the eyes pointing
anteriorly.
This subspecies may be known as P. putorius manium.
I take as the type no. 2. 8. 4. 24 (a male), procured by
Mr. Zollikofer at Teufin, Apfenzell, Switzerland.
The dimensions are:—Head and body 408°>mm.;_ tail
(without end-hairs) 145; hind foot 62; ear 25.
It seems probable that a paper by M. Drion, Jun.*, in
which he distinguishes a yellow and a black race of polecat,
both existing in Belgium, but with different habits, habitat,
and character, was based upon the overlapping and inter-
grading of these or other continental races. M. Drion states
that in both of his races he found the male about one third
larger and stouter than the female, and the young dark in
colour and hardly assignable to either form.
The large weasel named by Pallas Mustela sibirica, and
which has a wide range in Siberia, seems to be divisible
into a number of subspecies. In this animal there is probably
a considerable difference between the summer and winter
coats, the former being some shade of brown, the latter of
yellow. I find two forms which cannot be identified with
any previously published description of any known subspecies.
These are :—
Putorius sibiricus noctis, subsp. n.
Form as in P. sibiricus typicus.
Coloration. Above near “ vandyke-brown,” shading grad-
ually without line of demarcation into a tint between “ russet ”
and “tawny olive” beneath; the taila shade lighter than the
brown of the upper surface, but with the tip darker. Anterior
’
* Bull. Acad. Roy. Sei. Lett. Beaux-Arts Belg. sér, 3, t. xiv. pp. 365-
368 ; translated in ‘ Zoologist,’ 1895, pp. 866-869,
new Species and Subspecies of Mustelidie. 391
half of interramia, edges of lower lips, angles of mouth,
and a sprinkling of hairs about the nose white.
Dimensions: from label, ‘length 20 inches” ; hind foot
(measured in dried skin) without claws 54 mm.; tail (ditto)
including end-hairs about 170; ear about 15.
The skull is not perfect, but presents the following dimen-
sions :—palatal length 25 mm. ; zygomatic breadth 31. The
mesopterygoid fossa is attenuated anteriorly; the incisive
foramina are ample and elongated.
Type (an almost mature male), no. 99. 3. 1. 11, from
San-yen-tze, China, 5th August, 1896; procured by
Mr. F. W. Styan.
Putorius sibiricus noctis is clearly separated by its dull
coloration from all its allies of the Asiatic mainland. The
type is evidently in summer coat.
Putorius sibiricus miles, subsp. un.
Form as in P. sibiricus typicus.
Coloration. Above between “russet”? and ‘ cinnamon.
rufous,” shading into “orange-rufous” or “ochraceous
rufous” on the underside, and becoming darker on the upper
surface of the head. Upper surfaces of the feet, interramia,
upper lips, and a spot behind each nostril dirty white, shading
into ochraceous tints on the throat.
Dimensions from the dried skin:—Hind foot 45 mm.;
ear 15.
There is no skull.
Type. No. 74. 1. 16. 2, from Dauria, Eastern Siberia ;
received from Professor 'laczanowski.
The bright underside of this weasel renders it distinguish-
able at a glance from all other described forms.
Turning to the true weasels, I may remark here that the
subspecific name Putortus nivalis italicus proposed by me
for the Italian weasel is preoccupied by Achille Costa’s
name ‘ var. meridionalis” *, of which it must accordingly
stand as a synonym. The type locality of P. nivalis mert-
dionalis is ‘in Italia meridional continentalt.”
Amongst the ermines or stoats I find the following forms.
Firstly, a specimen from British North America does not
agree with any description by American naturalists of the
* Ann. del Museo Zool. della R, Uniy. di Napoli, anno 1865, p. 40
(dated 1869),
392 Mr. G. E. H. Barrett-Hamilton on some
various forms which inhabit that continent. It may be
known as
Putorius arcticus imperit, subsp. n.
Form as in P. ermineus or arcticus, but smaller and with
the tail longer than that of the latter.
Coloration of type specimen. Upperside (with exceptions
to follow) golden brown (between “tawny olive,’ “raw
umber,” and “ mars brown”), the crown of the head darker.
Dorsal borders of ears, a tuft of hairs at their anterior angle
on each side, upper lips, chin, interramia, and upper throat
white. Underside (except as above) deep “ primrose-yellow,”
including the inner and posterior surfaces of the fore legs, the
whole of the fore feet, the distal half and inner side of the
hind feet, and the under surface of the tail nearly to the dark
pencil. Line of demarcation well defined and straight, the
brown colour not encroaching on the underside. ‘Tail with
conspicuous dark terminal pencil.
The skudl corresponds with Dr. Hart Merriam’s description
of that of P. arcticus.
Dimensions of the type (taken from the dried skin) :—
Hind foot 88 mm.; ear 20; tail (including terminal hairs)
129; tail-pencil 71.
The somewhat damaged skull has:—Zygomatic breadth
25 mm.; palatal length 17; length of upper molar series 11,
of lower molar series 12.
Type. No. 63. 10. 28. 1, from Fort Simpson, British
Columbia; received from Mr. B. R. Ross.
P. arcticus imperti appears to be a smaller race of P. arc-
ticus, from which it differs also in the possession of white
ear-borders and upper lips, a less deeply yellow underside,
and a longer tail.
Secondly, the specimens long since brought home by
Mr. H. C. Hart from Greenland show that there are in that
country two forms of stoat. Of these the first is a well-
defined species, apparently not very clearly related to its
allies either of the Old World or of the New. It may be
known as
Putortus audax, sp. n.
General characters.— Size moderate ; tail short, with well-
developed dark pencil ; colours of upperside not encroaching
upon underside.
Coloration. Above between “ wood-brown” and “ mars
new Species and Subspecies of Mustelide. 398
brown,” the line of demarcation straight and decided. Below
white, tinged with yellow on the flanks, neck, and near the
legs, the white colour including also the upper lips, fore and
hind feet (but not conspicuously), the inner and anterior
surfaces of the limbs, but not the under surface of the tail,
which is barely lighter than the upper surface. Tail with
dark pencil commencing at about the middle point. Underfur
of upper surface near white.
The skull, as compared with that of American stoats, is
characterized by its broad, somewhat massive, and depressed
rostrum and moderately conspicuous postorbital processes.
It is shorter and far less massive than that of P. ermineus;
the posterior region has a peculiar rounded appearance when
viewed from above, which is characteristic, but difficult to
describe. The audital bulle are shortened as compared with
those of P. ermineus.
Dimensions of the type (taken from the dried skin) :~—
Hind foot (without claws) 40 mm.; tail (including terminal
hairs) 196 ; tail-pencil 63.
The somewhat damaged skull has a zygomatic breadth of
about 25 mm.; palatal length 18; length of upper molar
series 10°50, of lower molar series 12.
Type. No. 78. 6, 26.5; secured by Mr. H. C. Hart at
Discovery Bay, North Greenland.
A second skin was brought home by Mr. Hart from latitude
82° N., longitude 59° 20’ W., in Hall Land, in the very far
north of Greenland. This specimen appears to me to be a
form of P. arcticus, Merriam, and I accordingly propose for
it the subspecific name
Putorius arcticus polaris, subsp. n.
Form and general characters as in P. arcticus, Merriam.
Coloration. Above golden brown, the underfur near
white ; upper lips, interramia, and upper throat white; re-
mainder of underside deep “ primrose-yellow,” this colour
running in a slightly lighter shade to the underside of the
tail (except the terminal pencil) and the fore feet. Line of
demarcation direct and as in P. audaz.
There were no dimensions or skull with this speciinen. In
the dried skin the hind foot measures about 38 mm. and the
tail (including terminal hairs) 105, with a pencil of 62.
Type. No. 78. 6. 19. 11; locality as above.
Ann. & Mag, N. Hist. Ser. 7. Vol. xiii. 26
394 On some new Species and Subspecies of Mustelide.
Lastly, I find that true P. ermineus of Scandinavia * may
be distinguished from its southern representatives, such as
those of Britain, by the fact that it has the underside of the
tail (except the distal part occupied by the terminal pencil)
of the same colour as the underside generally, whereas in
British stoats the tail (except in cases of winter whitening)
is unicoloured all round. A second, and, to my mind (since
it is of deep physiological significance), far more important
distinction is the absence of winter whitening in southern
stoats. Southern examples may therefore be distinguished
subspecifically under the name of
Putorius ermineus stabilis, subsp. n.,
with no. 98. 5. 13. 2 (a female, dated the 18th of February,
1895), from Blandford, Dorset, presented by Mr. J. C. Mansel-
Pleydell, as the type.
IT add a description of the British stoat, not taken from the
type, but from a series :— ;
Coloration. Entire upper surface of both sexes (except the
end of the tail) in summer with the long outer hairs between
“mummy brown” and ‘‘ mars brown,” the underfur lighter
and near ‘isabella colour,” usually concealed, but in speci-
mens in old faded cvat showing through the thin outer hairs.
Under surface (except that of the tail) white, with a strong
wash of yellow which about reaches ‘ primrose-yellow” in
extreme, but by no means rare, cases at all seasons, the white
colour extending to the upper lips and the inner surfaces of
all four legs to the ankles and wrists, but not to the tail.
Line of demarcation definite and decided, the brown colour
not encroaching upon the underside. Tail with the hairs
* The nomenclature of the northern stoats must be regarded as en-
tirely provisional. Dr. Merriam clearly emphasizes the close relationship
between his arcticus and true ermineus by the remark that the former,
“though specifically distinct, is strictly the American representative of
the Old-W orld erminea” (‘ North-American Fauna,’ no. 11, p. 16, 1896),
Remembering, then, what different conceptions are prevalent between
naturalists of the Old and New World in regard to tne uses of specific
and subspecific names, that Baird’s Pudortus Kaneti (‘ Mammals of North
America &e., pp. 172-8, 1859) of Chukchi-Land and Bering’s Straits
(Arikamtchitchi Island) is a small yet ‘ perfect miniature” of ermineus,
and that Dr. Allen cannot find any tangible characters whereby to separate
stoats from North-eastern Siberia and Europe (Bull. Amer. Mus. N. Hist,
vol. xix. art. iv. pp. 174-176, March 31, 1903), we may look forward to
the strong possibility that both Kanew and arcticus with all its subforms
may eventually find their true status as subspecies of ermeneus.
Bibliographical Notices. 395
beginning to lengthen and deepen in colour at a point about
halfway from the extremity until they form a large black
terminal tuft or pencil, having a variable length, but often
reaching 100 mm. Feet often, but variably, white, either
partially or wholly. In winter the white of the under surface
may extend upwards, according to locality, until the animal
becomes completely white or white washed with yellow, the
black tuft of the tail alone retaining its dark colour. ‘The
margins of the ears, being amongst the first to whiten, show
this colour to a variable extent in many specimens otherwise
apparently in full summer coat; for a similar reason the feet
may be partially white at all seasons of the year.
The average dimensions (in millimetres) of a series are
(approximately) :—
Skin, Skull.
—— AS === (Ss e's a
Head and Hind Greatest Basal Palatal Zygomatic
body. Tail. foot. Ear. length. length. length. breadth.
Males .. 269 BEL 48 22 ~=—s«éB ETS SO 22
Females, 244 90 42 20 46 42 25 19
BIBLIOGRAPHICAL NOTICES.
Mostly Mammals. By R. Lypuxxer. Pp. 383; 16 plates.
London: Hutchinson & Co. 1903.
To a very large number of readers the essays in this volume will be
right heartily welcomed as old friends finally united under peculiarly
happy circumstances. By a careful process of gleaning from the
pages of ‘ Knowledge,’ ‘ Nature,’ ‘The Field, and ‘The Asian,’
Mr. Lydekker has produced a really delightful volume. Full of
matter for thoughtful consideration, it will be cherished as guide,
philosopher, and friend by those who live in the country, or are
called away into wild places far from the haunts of men, where
books are not, save those that are carried for their own intrinsic
worth.
Perhaps the most fascinating chapters in the volume are those
referring to the coloration of animals. Save the chapter on
cowrie-shells, mammals only are dealt with under this head, but, as
many will know already, these chapters are strikingly original and
suggestive.
To the traveller the chapters on ‘ Celebes: a Problem in Distri-
bution ” and “ Deserts and their Inbabitants” will serve as incen-
tives to observation, no less than those on coloration; whilst the
896 Bibliographical Notices.
stay-at-home naturalist will find equally helpful studies in’ the
essays on domesticated animals. But these are by no means the
only subjects treated of in this volume. Extinct animals, armour-
clad whales, monkey finger-prints, frogs and toads, and scorpions
are amongst the other subjects noticed, and all alike are of ex-
treme interest.
The book is well printed, tastefully got up, and well illustrated,
there being no less than sixteen full-page plates, the most remark-
able of which is a photograph showing giraffes in covert. ‘The
volume would make a handsome gift-book,
Catalogue of the Lepidoptera Phalene in the British Museum.
Volume IV. Cataloque of the Noctuide in the Collection of the
British Museum, By Sir Grorce F, Hampson, Bart. London:
Printed by Order of the Trustees, 1903. 8vo. Pp. xx, 689.
Plates lv.—lxxvii.
Wa congratulate Sir George Hampson and the authorities of the
British Museum on the publication of the fourth volume of the
great Catalogue of the Moths of the world, which has been appearing
at intervals during the last six years. With Volume LY. the great
family of Noctuide is commenced, with one of the largest and most
importaut of the subfamilies, the Agrotine, of which no less than
1126 species are described, by far the larger proportion of which
have only been made known within the last few years. ‘To the
entomologists of the present day, the wonderful increase in our
knowledge of insects and the large collections now in existence
appear marvellous. So did Hewitson’s collection of Exotic Butter-
flies to the older generation of naturalists who were his contem-
poraries; but hundreds of the most beautiful butterflies in the world,
which are now to be found in every first-rate collection, were either
unique and unattainable, or undiscovered in his time, and he did not
live to see them. Our knowledge of moths has also very largely
increased, though it cannot be supposed to be so forward as in the
case of butterflies, for three reasons: firstly, because they are much
more numerous; secondly, because many of them are less brightly
coloured, and thus less attractive, and are therefore less assiduously
collected; and, thirdly, because many are nocturnal insects and are
therefore really more difficult to collect. But nothing is more likely
to encourage and extend the knowledge of moths than comprehensive
and well-illustrated works like Sir George Hampson’s.
In addition to the coloured plates, there are 125 text illustrations,
representing structural details. Many larvee are described, those of
North-American species by Dr. Harrison G. Dyar; but there are no
illustrations of larvee, which the character of the book would perhaps
hardly admit of. Very full tables of species are given under genera,
or, in the case of the larger genera, under sections; and we are glad
to notice that when a number of generic names are included under
@ more comprehensive one (as in the case of Huwoa, Hiibn., p. 153)
Bibliographical Notices. 397
the types of the various names are indicated. This will be very
useful for future reference.
At the end of the volume we find a list of unrecognized species,
some of which will probably be identified and referred to their
proper position at some future time.
The Fauna of British India, including Ceylon and Burma. Pub-
lished under the authority of the Secretary of State for India in
Council. Edited by W. T. Branrorp.—Rhynchota. Vol. IL.
Part 1 (Heteroptera). By W. L. Distanr. London, 1903.
Pp. xP 242% figs. 167.
As we are informed that the next part of this work, completing the
second volume, will appear very shortly, we will defer our detailed
notice until then, and confine ourselves for the present to recording
the publication of the present instalment, which extends from
Fam, 4. Lygeidw to the commencement of Fam. 12. Reduviide.
Memoirs of the Geological Survey.—Paleontologia Indica. Series 1X.
The Jurassic Fauna of Cutch. Vol. ILI. Part 2. The Lamelli-
branchiata. No. I. Genus Trigonia. By F. L. Krreury, M.A.,
Ph.D., Geol. Survey England. 122 pages, Fol. Plates I.-X.
Calcutta, London, and Berlin, 1903.
Tur Trigonie of Cutch here figured and described have been selected
from among the Lamellibranchs collected by Wynne, Tedden,
Stoliczka, and Blanford, and entrusted to Dr. Kitchin, of London,
for examination and description. The strata from which they came
are known as the following groups :—I. The Oomia group, probably
combining the Cretaceous, Neocomian, partly the Portlandian ;
Il. The Katrol, probably combining the Kimmeridgian and Ox-
fordian, and constituting the Upper Jurassic of Cutch; III. The
Charee, probably representing the Kelloway strata, Middle Jurassic
of Cutch ; LV. The Patchum, probably representing the Bath Oolite
group. These are enumerated in the second edition of the ‘ Manual
of the Geology of India,’ 1893, p. 217.
The classification of the known fossil Trigonie into sections,
groups, and genera is carefully considered and clearly explained. In
some cases these serial divisions and subdivisions of recognized
forms are separated from their several allies by gaps variable in
extent and value, but evidently reducible by better knowledge of
the types. The most reliable observers and authors concerned in
this classification have been :—Agassiz, 1840; d’Orbigny, 18438 ;
Pictet, 1866; Stoliczka, 1871; Lycett, 1872-1883; Bayle, 1878;
Choffat, 1885; and Bigot, 1892. Their methods and results are
succinctly stated at pages 7-9.
The differences due to the progress of growth in individuals (as in
growth-stages) are taken into consideration on the lines more or
398 Bibliographical Notices.
less definitely indicated by Hyatt, 1888; Jackson, 1890; and by
Buckman and Bather, 1895, for other kinds of Mollusca.
A strict comparison of the species from Cutch with those at present
known. from other parts of the world is made throughout. The
Distribution of the fossil Trigonie in Cutch is thus given at pages
12 and 120 :—
a. (i) Costote (Section).
1. Trigonia tumida, nov.
T. prora, n.
3. T. chariensis, n.
4. T. propinqua, n.
d. T. brevicostata, n.
6. T. distincta, n.
7. T. acuta, n.
8. T. dhosaénsis, n.
9. T. nitida, n.
LOM sp:
lL. T. tenuis, n.
12. T. parva, n.
( Patehum Group.
12. ...4 Charee Group.
Oomia Group.
(ii) Derivatives of Costate (Section).
13. Trigonia Smeei, J. de C. Sowerby.
14, T. crassa, n.
15. T. cardiniiformis, n.
16. 'T. trapeziformis, n.
17. T. retrorsa, n.
b. Gibbose (Group).
18. Trigonia spinicostata, n.
5... Oomia Group.
1... Oomia Group.
ec. Group of Trigonia v-scripta (Group).
19. Trigonia dubia, n.
20. T. v-seripta, n.
Y1. 'T. recurva, n.
d. Undulate (Section).
22. Trigonia remota, n.
Oomia Group.
1... Oomia Group.
e. Scaphoidee (Section).
(Sensu latiore.)
23. Trigonia kutchensis, n.
24, T. exortiva, n.
25. T. hispida, n.
26. 'T. jumarensis, n.
27. T. gracilis, n.
Or
Patchum Group.
*** | Charee Group.
f. Pseudo-quadrate (Group).
28. Trigonia mamillata, n. :
n po yee aoe oes‘ a sO SOOO a ee ee a
ies)
1... Oomia group.
g. Scabre (Section).
29. Trigonia yentricosa, F’. Krauss, sp.
80. T. pulchra, n.
I. Nos. 1, 2, 25, 26 occur in the Upper Patchum beds.
II. Nos. 1, 3, 4, 5, 6, 7, 8, 9, 10, 23, 24, 27 occur in the Charee
group.
III. None in the Katrol group.
IV. Nos. 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 23, 28, 29,
30 occur in the Oomia group,
Oomia Group.
SS
bo
Geological Society. d99
Of these thirty species only two were determined as occurring
in Cutch previously, namely Z’rigonia Smeei and VT. ventricosa. The
former has long been known as an Indian Species, and the latter
also in India as well as in the Uitenhage strata of South-east Africa,
and lately it has been found in German East Africa.
In the Appendix at page 121 Dr. Kitchin refers to the Mesozoic
Mollusca collected during W. Bornhardt’s J ourney in German East
Africa (1895-97), and described by Dr. G. Miiller in 1900, who
regards two of the species as J urassic; but two of the others he
considers to be of Lower Neocomian age, namely 7’. ventricosa,
Krauss, and its associate 7. Beyschleyi, Miiller. 7. Kuchni, Miiller,
is said to be of Upper Neocomian age. It is evidently certain that
there is a resemblance (Dr. Kitchin says) of the German Kast-
African fossils to those of the Ooinia group and those of Uitenhage,
as far as the lamellibranchs bear evidence at present (pages 2, 115,
121, &c.).
The tere figures of Trigonie in the ten lithographic plates
are excellently well drawn, of natural size, by Miss G. M. Wood-
ward, of London.
Circulars on Agricultural Economic Entomology.
Issued by the Trustees, Indian Museum.
We have received the following numbers of these useful publications,
which are accompanied with good recognizable uncoloured illustra-
tions, and are issued at the price of 3 or 4 annas per dozen, fur
general circulation in India.
No. 1. The Rice Sapper (Leptocorisa acuta),
The Bengal Rice Hispa (Hispa cenescens).
. The Sugar-cane Borer (Chilo simplex),
. The Rhinoceros or Date-Palm Beetle (Oryctes rhinoceros),
- The North-west or Migratory Locust (Acridium pere-
grinum).
The Cut-Worm (Agrotis ypsilon).
OV op bo
=
PROCEEDINGS OF LEARNED SOCIETIES,
GEOLOGICAL SOCIETY,
January 20th, 1904.—Sir Archibald Geikie D.C.L., D.Se., Sec.R.S.,
>
Vice-President, in the Chair.
The following communication was read :—
‘On the Jaws of Ptychodus from the Chalk.’ By Arthur
Smith Woodward, LL.D., F.R.S, F.LS., F.GS,
Hitherto no traces of the cartilaginous jaws of this fish have been
found in association with the dentition; but Mr. Henry Willett has
409 Geological Society.
recently found a specimen of Ptychodus decurrens, in the zone of
Holaster subglobosus of the Lower Chalk at Glynde (Sussex), Frag-
mentary remains of both jaws are seen in the specimen, each bearing
many of the characteristic teeth arranged in natural order. There
are four series, and one small displaced tooth (probably belonging to
the fifth series), on the left of the large median series in the lower
jaw; while in the upper jaw the teeth are clearly arranged in six paired
series. The specimen proves that the peculiarly effective disposition
characteristic of the living Myliobatidee had not been assumed, but
that Ptychodus more nearly resembled the Trygonid in its jaws.
The probable explanation of the new discovery is, that in the
Cretaceous Period, the great Rays of the ‘families’ Myliobatide and
Trygonide had not become fully differentiated, Prof. Jekel has
already arrived at a similar conclusion from general considerations,
and has proposed to place all these fishes in one comprehensive
family, termed Centrobatide. If this arrangement be adopted,
Ptychodus represents a primitive sub-family, which still awaits
definition from lack of complete specimens ; while the Trygonina,
Myliobatinee, and Ceratopterinze are equivalent sub-families which
survive at the present day.
‘April 13th, 1904.—J. KE. Marr, Se.D., F.R.S.,
President, in the Chair.
The following communication was read :—
‘The Discovery of Human Remains under the Stalagmite-Floor
of Gough’s Cavern, near Cheddar.’ By Henry Nathaniel Davies,
Esq., F.G 8.
Gough’s Cavern opens at the base of the cliffs on the south side of
Cheddar Gorge. Various human and animal remains have been
discovered at different times in the clearing-out of parts of the
main cavern. ‘The principal deposits are a stalagmite-like travertine
overlying cave-earth, and the latter at one place encloses a tabular
limestone-block surrounded with flint-chips. During drainage-
operations it was found necessary to excavate part of a fissure
running northward out of the vestibule of the cavern, when a human
skeleton was discovered, associated with flakes, scrapers, and borers of
flint, embedded in cave-earth, which overlay a lower bed of stalag-
mite and was overlain by a second bed 5 inches thick. The
skeleton was nearer the top than the bottom of the deposit, and the
remains excavated comprise the skull, the bones of an arm, a leg,
and part of the pelvic girdle. The other bones were allowed to
remain in situ, and may now be seen. ‘The position of the skeleton
was that which would have been assumed by a drowned man,
Interment is out of the question, because of the narrow and steep
shape of the fissure, which was choked up with undisturbed debris
and caleareous deposits. The stature of the man was 5 feet 5 inches ;
Miscellaneous. AOL
he was of muscular build, with prognathous jaws, a straight thigh,
an extremely platyenemic tibia, and a thick dolichocephalic skull.
The animal-remains found in the cave-earth of other parts of the
Cavern, and held by the Author to be contemporaneous with that
in the fissure, are those of mid- and late Pleistocene age ; and this
evidence, together with that derived from the position of the skeleton,
the shape of the cranium, and the form and workmanship of the
flakes, points to a period towards the close of the Paleolithic or the
opening of the Neolithic Age.
MISCELLANEOUS.
The Action of Human Serum on certain Pathogenic Trypanosomes ;
Action of Arsenious Acid upon Trypanosoma gambiense. By
A. Laveran.
In previous notes (1st April, 1902, and 6th July, 1903) I have
shown that human serum injected in sufficient doses into mice or
rats affected with Nagana, Mal de Caderas, or Surra, caused the
Trypanosomes to disappear, at least temporarily, from the greater
circulation.
A mouse weighing 20-25 grammes required 0:5 to 1 cc. of
human serum; a rat of 200 grm., 2-3 ¢.c. of serum or 0°20-0°30
grm. of dry serum in powder.
_ The Trypanosomes disappear in 24 or 36 hours from the larger
circulation, but reappear in general at the end of a few days.
Sometimes their disappearance is definitive. The most frequently
repeated injections of human serum do nothing more than prolong
the life of the animals.
In the month of November, 1903, Drs. Dutton and Todd sent me
through Dr, Annett two rats, one infected with Zrypanosoma gam-
biense, the other with a Trypanosoma of horses from the Gambia.
It appeared demonstrated that 7’. gambiense, discovered by Forde and
Dutton in Gambia, is identical with the Zrypanosoma described by
Castellaini under the name of Zr. ugandense, as the pathogenic
agent in the disease called ‘sleeping sickness.” The study of this
parasite is therefore, from the medical point of view, of great
interest.
One might think, @ priori, that Tr. gambiense, which is developed
in the blood of man, as in that of many other mammals, would not
be influenced by human serum, contrary to that which takes place
in the case of the Trypanosomes of Nagana, Surra, and Caderas,
diseases against which man is naturally immune. This is precisely
the result of my observations. Human serum injected in doses of
0:20-0:30 grm. of the powder, in the case of rats weighing 170 to
200 grm. infected with 7’r. gambiense, proved entirely inactive.
At the beginning of the infection of rats with Zr. gambiense, the
Trypanosomes are very rare in the blood, and it happens that after
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 27
402 Miscellaneous.
examinations giving positive results, subsequent examinations yield
negative results; but at the end of a month or six weeks the
Trypanosomes have established themselves in the blood, and their
number is, in general, large enough to enable the action of medica-
ments to be readily observed ; and this is the time to be chosen for
experiments with drugs and serums.
Fresh serum of guinea-pig, sheep, and horse proved without
action upon J'r. gambiense, like human serum; this was to be ex-
pected, because the guinea-pig, sheep, and horse can alike be infected
with 7. gambiense.
P. Manson tried the treatment of a case of injection by Trypano-
soma with injections of horse serum, but failed (Brit. Med. Journ.
30 May, 1903); the result might have been foreseen, the horse not
being refractory to infection by 7r. gambiense (Dutton and Todd,
Ist. Rep. of the Trypanosomiasis Exped. to Senegambia, 1902,
Liverpool, 1903, exper. 87, pl. x.).
This Trypanosome develops unfortunately in the blood of most
mammals. I ought, however, to say that the serum of a Cyno-
cephalus, apparently naturally immune against 7’r. gambiense,
showed itself as little active as the serum of animals having an
admitted susceptibility to this Trypanosome.
It will be well to experiment with the serum of animals with
acquired immunity against Zr. gambiense and that of animals
made hyper-immune, but the results of previous researches in this
direction with other pathogenic Trypanosomes (Laveran and Mesnil,
“ Recherches sur Je traitement et la prévention du Nagana,” Ann.
de l’Instit. Pasteur, Nov. 1902), and of some trials of the curative
power of serum of animals with acquired immunity against 7’r,
gambiense itself, leave but small hope of a definitive result of such
experiments.
Human serum, inactive against 7. gambiense, has, on the con-
trary, an evident though feeble action on the Trypanosoma of horses
in the Gambia. It is now demonstrated that this latter Trypano-
some must be completely separated from 7’. gambiense, from which
it is distinguished by its morphological characters, as well as by its
pathegenic action on animals; but at the outset of their researches
Dutton and Todd have placed the question of the identity or non-
identity of these parasites observed in the same region. Their
different reaction with human serum provides a fresh proof in
support of their differentiation. Human serum injected in suffi-
ciently large doses into mice and rats having a fair number of the
Gambia horse Trypanosomes in their blood, generally causes these
Trypanosomes to disappear in 36 or 48 hours; but the parasites
do not fail to return.
In the cases where the Trypanosomes are numerous, the injection
of human serum can only have for result a diminution of their
number. ‘The activity of human serum is, in short, real but more
feeble than in the case of Nagana, Surra, and Caderas.
Arsenious acid is the only drug which has given any favourable
results in the treatment of Surra and Nagana (op. cit., Ann. de
Miscellaneous. 403
l’Inst. Pasteur, Noy. 1902); it was therefore of interest to experi-
ment on its efficacy agaiust 7’r. gambiense.
It results from experiments which I have made on rats that
arsenious acid, given in suflicient doses, causes the 7’. gambiense to
disappear from the greater circulation, at least in a temporary
manner, and that it can hasten the cure of Trypanosomiasis in these
animals. The efficacious dose is 0:1 mgr. of arsenious acid for
every 20 grm. of animal, 2. e. 1 mgr. for a rat of 200 grm.; below
this dose the results are nil or incomplete.
(Note.—This is also the efficacious dose in Nagana, Surra, and
Caderas. The solution employed for hypodermic injection has the
following composition :—-Arsenious acid 1 grm., carbonate of soda
1 grm., distilled water 500 grm.—Laveran and Mesnil, op. cit.)
In human Trypanosomiasis arsenical compounds have been often
tried and have yielded only a passing amelioration, but in general
the doses prescribed have been too feeble. Judging by the results
of experiments on animals, one may say that the method which
consists in giving small daily doses of arsenious acid (the method
most frequently adopted in the treatment of human Trypano-
somiasis) is bad, and that it is preferable to administer large doses
at longer intervals.
Writers are all agreed that human Trypanosomiasis is always
fatal as soon as the nervous symptoms declare themselves, but
before the appearance of these symptoms there is a period, more or
less long, during which the Trypanosomes, in small number in the
blood, produce but few morbid troubles. In this first phase it is
probable that the infection produced by Zr. gambiense is curable in
the human subject as it is in many species of animals, and that
arsenious acid may contribute to a cure.
Good hygienic conditions and abundant food are also important
factors in the treatment of Trypanosomiasis; in Africa the ‘“ sleeping
sickness ” rages with a peculiar intensity among the miserable Negro
labourers, overworked and ill-fed. (Note—Christy, Rep. of the
Sleeping Sickness Comm., Nov. 1903: in Uganda the epidemic of
Trypanosomiasis has been greatly aggravated by famine.) The
same thing is observed among animals, those that have some defect
or some cause of enfeeblement are more strongly infected than
those which are in good condition and are supplied with abundant
tood.—Comptes Rendus, tome cxxxviil. p. 450 (22 Feb., 1904).
Relations between the Development of the Tracheal Apparatus and
the Metamorphoses of Insects. By Jutus Anetas.
The phenomena of internal metamorphosis have in Insects a strict
relation to the development of the respiratory apparatus.
The metamorphoses properly so-called, characterized by the phe-
nomena of histolysis followed by histogenesis, bear, moreover, even
among the Holometabolids, only on the middle portion of the
intestine, the muscles, and sometimes on the tracheal apparatus
itself.
In the Hymenoptera that I have studied (Wasps, Bees) these
404 Miscellaneous.
phenomena always correspond with the centripetal tracheal growths.
Shortly after the hatching of the larva a first growth of tracheal
tubes makes its appearance towards the mid-intestine. At this
moment, at the base of the epithelial cells of that organ, appear the
elements of future substitution. A careful study of sections shows
that the substitution-cells communicate with the ultimate and very
delicate prolongations of the tracheal tubes. They may therefore
be regarded as tracheal cells analogous to those seen along the
course or at the extremities of the tracheal tubes.
The elements of substitution are in a state of rest all through
the life of the larva; but from the beginning of nymphosis a
renewal of activity sets in: they proliferate actively, join one
another and constitute the definite digestive epithelium, whilst
the larval tissue enters into histolysis and is thrown off. <A fresh
tracheal growth appears at this moment; the calibre and arrange-
ment of the respiratory apparatus are modified. At the same time
fine tracheoles proceed in great number towards the peri-intestinal
muscular layer and penetrate it; the same occurs in the other
muscles of the thorax and abdomen.
The terminal tracheal cells, or even the cells of the wall of the
tracheal trunks, insinuate themselves into the sarcoplasm of the
muscular fibres, there multiply actively and form long linear
threads ; so that the larval fibre is cut up into little columns, broken
up and profoundly altered in form. In the muscular histolysis,
whether partial or total, the tracheal cells play an important rdle
by a mechanical process, and probably also chemical, but without
the phenomena of phagocytosis.
Many of the tracheal cells become free in the general cavity and then dis-
appear on the spot; others furnish the tracheoles of the muscles of the imago,
these latter turning out the corresponding larval elements (larval muscular
fibres and nuclei),
An American observer, Robert 8S. Breed*, has described analogous
processes in the muscles of a Coleopter (Z’hymalus). One is inclined
to ask with him if it would not be well, in considering the tracheal
elements, thus far too much neglected, to again take up the study
of the Diptera, in which it is classic to describe an intense phago-
cytosis during the metamorphosis.
In the Hymenoptera the metamorphosis which has just been sketched is
completed by the histolysis and total disappearance (without phagocytosis) of
the primitive Malpighian tubes and the salivary glands. In short, a burst of
ectodermic activity realizes the completion of the following organs, momentarily
retarded in the larva: teguments, appendages, esophagus, rectum (formation
of fresh Malpighian tubes), nervous system, and sense-organs.
The tracheal growth is itself a manifestation of this ectodemic
activity. It is to be remarked that it corresponds with a period
during which Bataillon has noted asphyxial respiratory troubles in
Bombyx mori.—Comptes Rendus, tome exxxviii. p. 300 (1 Feb.,
1904).
* R.S. Breed, “The Changes which occur in the Muscles of a Beetle”
(Bull. Mus. Comp. Zool. Harvard Coll, vol. xl. no. 7, Oct. 1903).
Ann. & Mag. Nat. Hist. 8.7. Vol. XM. PUVIL
Mintern Bros imp.
J, Green del.et lith,
PeuPHuRus GLADE.
THE ANNALS
AND
MAGAZINE OF NATURAL HISTORY.
[SEVENTH SERIES.]
No. 78. JUNE 1904.
XLVIL.—On Mammals from Northern Angola collected by
Dr. W. J. Ansorge. By OLpFreLD THomas.
Duriné 1903 the well-known collector Dr. W. J. Ansorge,
to whom the British Museum is already indebted for series
of specimens from British Hast Africa, Uganda, and Nigeria,
made a collecting-trip to Northern Angola, and obtained
about two hundred specimens belonging to forty-six species,
and of these a complete set has been acquired for the Museum.
The mammalogy of Angola has hitherto remained almost
entirely in the hands of the Portuguese, as represented—most
admirably—by Prof. Barboza du Bocage in Lisbon and by
M. Anchieta and other collectors in the country under con-
sideration. ‘Thanks to the enlightened generosity of Prof.
Bocage many institutions, and notably the British Museum,
had received specimens representing the species discovered in
Angola by the Portuguese naturalists, and on these specimens
such comments on the Angolan fauna as have been made by
Gray, de Winton, myself, and others have been based.
But these specimens, valuable as they have proved to be,
have been all preserved in spirit, and the freshly made skins
obtained by Dr. Ansorge are therefore of very great interest
for comparison with similarly made specimens from other
regions of Africa.
Complete as have been Prof. Bocage’s researches on the
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 28
406 Mr. O. Thomas on
subject, the present collection contains a fair number of
species not included in his lists, while, owing to my having
been able to compare the remainder directly with typical
specimens from other localities, I have found it necessary to
describe several of those he mentions as local species or
subspecies.
Dr. Ansorge has therefore to be congratulated on the
considerable number of new and interesting forms which his
collection has enabled me to discriminate.
1. Miopithecus talapoin, Eirxl.
g. 200. Canhoca.
2. Rousettus collaris, Ul.
3. 40. Pungo Andongo.
This specimen has a small third upper molar on each side.
3. Epomophorus pusillus, Peters.
&. 195, 196. Canhoca.
4, Epomophorus sp.
. 70. Pungo Andongo.
. 143. Braganza.
+0 OY
5. Epomophorus sp.
. 69; 2. 68,124. Pungo Andongo.
. 138. Braganza.
+0 OY
6. Hipposideros caffer, Sund.
9.5. Ambaca.
7. Hipposideros Commersont gigas, Wagn.
@. 201. Canhoca.
A note on the subspecies of H. Commersoni has been
recently published *.
8. Nycteris sp.
@. 58. Pungo Andongo.
Closely similar, both in size and colour, to the type of
N. ethiopica luteola, 'Thos., from British Hast Africa, but
from the single skin I do not venture definitely to assign it
to that form.
* Ann. & Mag. Nat. Hist., May 1904, p. 384.
Mammals from Northern Angola. 407
9. Pipistrellus nanus, Pet.
&. 71,72; 9. 73, 74, 84. Pungo Andongo.
6. 139; 2. 145. Braganza.
10. Myotis Bocaget, Peters.
do. 140,148; ¢@. 146,147. Braganza.
These specimens, actual topotypes, are of a far brighter
colour than those from the Cameroons, which, in the absence
of Angolan examples, we had hitherto treated as the true
Bocaget.
The Cameroon form would appear to represent a special
subspecies, as follows :—
Myotis Bocaget cupreolus, subsp. n.
Essential characters as in true 1. Bocage?, but the colour
much darker, owing to only the terminal millimetre instead of
2-3 mm. of the dorsal hairs being reddish; the reddish is
also of a more coppery tone. A blackish patch at the base of
each humerus. Under surface dark smoky brown, the hairs
being dark smoky with brownish tips; inguinal region not
or scarcely lighter. In true Bocage? the under surface is pale
buffy brown.
Dimensions of the type :—
Forearm 39 mm.
““ Head and body 60”; “tail 40”; “ear 15.”
Skull: greatest length 15.
flab, Efulen, Bulu Country, Cameroons.
Type. Male. B.M. no. 3. 2.4.6. Collected 14th August,
1901, by Mr. G. L. Bates.
11. Miniopterus Schreiberst, Kuhl.
2. 202, 203. Golungo Alto.
12. Nyctinomus limbatus, Pet.
dg. 215. Cunga.
2 (in spirit). 2. Loanda.
13. Laphozous mauritianus, Geoff.
?. 1. lLoanda.
14, Crocidura (Croc.) sp.
&. 20; ¢.17. Pungo Andongo.
?. 156. Braganza.
408 Mr. O. Thomas on
15. Viverra etvetta, Schr.
204. Golungo Alto.
?. 124. Pungo Andongo.
16. Genetia sp.
? (young). 180. Braganza.
? (young). 210. Golungo Alto.
17. Nandinia binotata, Gray.
205. Golungo Alto.
18. Herpestes galera, Erxl.
209. Golungo Alto.
19. Herpestes albicaudus loande, subsp. n.
9. 23. Pungo Andongo.
“Caught by native hunting dogs.” “Native name
mabeku.”—W. J. A.
The animals usually referred to H. albicaudus, ranging
from Senegal to Natal, are very uniform in colour, with the
striking exception of the condition of the tail, which may be
either black or white in the same locality. Broadly speaking,
the forms from N.E. Africa and Arabia, representing leucurus,
Hempr. & Ehr. (syn. albescens, Geoff., abu-wudan, Fitz.),
are paler and more buffy, while those from West Africa, East
Africa, and further south are more heavily blackened. The
skulls show the former to be rather smaller than the latter.
But in the dimensions and structure of the last lower
molar there are such striking and yet locally constant
differences that it is impossible to regard as identical all
a, Last lower molar, left side, of Herpestes albicaudus leweutus,
6. Ditto of H, a. loande.
the forms hitherto referred to the one species [7. albicaudus.
Treating them for the present as subspecies, the animal I
should call HZ. a. leucurus has the tooth small and narrow
Mammals from Northern Angola. 409
(6X3°7 mm.), low (height of hinder side of main antero-
internal cusp 3°2 mm.), and simple, the antero-internal cusp
not or scarcely divided into its constituent paraconid and
metaconid, the hinder rim of the talon little developed, and
with but one low cusp on the centre of the talon (see fig. a).
The opposite extreme to this is shown by my Herpestes
grandis (figured P. Z. §. 1889, pl. Ixii.), where the tooth is
very large (8:1 x 4:7 mm.), high, and complicated, the ante-
rior trefoil well developed, and the talon with a high posterior
rim subdivided into cusps behind, and with two cusps on the
talon, one on its outer edge and one in its centre.
Kast-A frican specimens have the tooth large (7°4 x 4:5 mm.),
but lower than in grandis, the paraconid and metaconid
distinct, the rim of the talon well defined, but not divided
into cusps posteriorly, and with one large cusp on the antero-
external part of the talon. ‘This form I would propose to call
IT. a. tbeanus *.
In specimens from Guinea, representing loempo, Temm.,
and perhaps the original Senegalese albicaudus, mz is of
medium size (7X 4°2 mm.), low, with the metaconid distinct
but lower than the paraconid, the median outer cusp high,
nearly equal to the low protoconid, the posterior rim of the
talon high and irregularly notched.
Finally, in the North-Angolan form (/. a. loande, subsp. n.)
the tooth is large (7°5 X4°8 mm.), but its cusps and crenula-
tions are remarkably low and indistinct, the paraconid practi-
cally coalesced with the metaconid, the median outer cusp low
end rounded, continuous with a low transverse crest running
transversely across the tooth, posterior part of talon narrow,
its rim formed of two low cusps (fig. 0).
The skull of this mungoose is large, and all the teeth are
heavy and well developed; but in the single example there
* Subsp. n. Colour intermediate between the pale North-eastern and
darker Western forms, though nearest the latter, the general tone of the
fur, apart from the dorsal black hairs, greyish isabella. Tail white in the
type. :
iineasiins of an adult skull (not the type), collected by Dr. J. W.
Gregory at Kibwezi, Kikuyu:— _
Basal length 100 mm. ; zygomatic breadth 51; front of canine to back
of m? 42; breadth of palate outside m? 53.
Dimensions of teeth in the type: greatest diameter of p* 10, m? 8-4,
pg 19, mM, 83, m, 74. :
Hab. East Africa. Type from Athi-ya~-Maui, Mombasa-Uganda
Railway.
Type. Immature male. B.M. no. 99.10, 14.2. Presented by C. 8.
Betton, Esq.
The object of selecting an immature specimen as the type is to have
one with the diagnostic tooth unworn,
410 Mr. O. Thomas on
is no trace on either side of the small anterior lower premolar,
a peculiarity not occurring in any other specimen of the
roup. ,
The general colour is dark grizzled grey, with black limbs
and white tail.
Dimensions of the type (measured in the flesh) :—
Head and body 620 mm.; tail506; hind foot 135; ear 47.
Skull: nasals 26 (in middle line) x10; interorbital
breadth 23 ; breadth of palate across outer corners of m* 35°5 ;
front of canine to back of m?41; greatest horizontal diameter
of p* 10, m? 8:3, pg 82, m, 8°9, my 75
Hab. Pungo Andongo, 1200 m.
Type. Subadult female. B.M. no. 4. 4.9.37. Original
number 23. Collected 6th June, 1903.
The above division into ‘ subspecies” is, of course, only
provisional, until such time as sufficient material is available
for the true relations of the different forms to be made out.
Probably the north-eastern type, paler in colour, rather
smaller, and with very small mp, should in any case be looked
upon as a distinct species. Whether it overlaps the larger
and darker animal remains to be seen.
20. Pecilogale albinucha, Gray.
178. Marimba, Jinga Country.
g. 179. Bange, Ngola, Jinga Country.
21. Scturus Nordhoffi, Du Chaillu.
gd. 199. Canhoca.
206. Golungo Alto.
22. Sciurus annulatus, Desm.
S$. 198. Canhocea.
23. Funisciurus congicus, Kull.
a. 197. ‘Canhoes.
24. Funisciurus congicus olivellus, subsp. n.
3. 214. Cunga.
In his classical paper on the mammals of Angola, Prof. du
Bocage stated that the squirrels he referred to Sccurus congicus,
Kuhl, presented several different types of coloration, and |
am inclined to think that these are so different as to deserve
recognition by name. For the moment I shall treat them as
subspecies of congicus, though I think it probable that when
Mammals from Northern Angola. 411
more localized specimens are brought together some of their
ranges will be found to overlap without intergradation taking
place, in which case they will have to be considered as species.
The three forms I recognize may be briefly indexed as
follows :—
Colour dark olivaceous, lateral lines blackish. Tail dull
PrBea ye TSE eee tava cia reto Sake, kv Pair ac)se! age Wich 80m micunretg congicus.
Colour light yellowish olivaceous, lateral lines scarcely
darkened. Tail-hairs ringed with black and yellowish. o/¢vellus.
Colour dull fulyous, the white stripes very broad. Tail-
hairs orange at their bases .......-.seesss sevens Jlavinus,
The Canhoca specimen of Dr. Ansorge agrees closely in
its general dull tone and the blackness of the outer dark line
with Kuhl’s type, still in the British Museum collection. A
specimen received from the Lisbon Museum, and labelled as
from Caconda, is also similar,
Funisciurus congicus olivellus, subsp. n.
General colour clear yellowish olivaceous, almost ap-
proaching Ridgway’s “ olive-yellow.” ‘This colour is yellower
on the sides of the nape and on the rump, darker on the back.
White stripe well defined, but narrow, the body-colour on
each side of it scarcely darkened. Flanks abruptly lighter.
Belly white, not sharply defined laterally. Cheeks light, an
indistinct darker line running through the eye. Limbs ex-
ternally like flanks, internally like belly; upper surface of
hands and feet yellow. ‘Tail-hairs ringed with pale yellow
and black, the bases, middles, and tips of the former colour
separated by two rings of black.
Dimensions of the type (measured in the flesh) :—
Head and body 165 mm.; tail 180; hind foot 36; ear 14.
Hab. (of type). Cunga.
Type. Adult male. B.M. no. 4. 4. 9. 45. Original
number 214. Collected 1st February, 1904.
The Museum contains another example of this form labelled
as from the Quanza River.
Funisciurus congicus flavinus, subsp. n.
J ’ P
S. congicus, var. flavivittis, Bocage (not S. flavivittis, Peters).
General colour strongly flavescent, approaching orange on
the sides of the neck and on the rump. White stripes very
broad and prominent, the dorsal colour between them suffused
with blackish; lateral lines outside them well marked,
blackish. Under surface buffy yellow, as are also the inner
Ate Mr. O. Thomas on
sides of the limbs; upper surface of hands and feet orange-
yellow. Sides of head and edges of ears dull buffy whitish, a
faint darker line running backwards from the whiskers and
another through the eyes. Tail-hairs deep orange for their
basal half, then with a broad subterminal bar of black, their
tips buffy yellow ; terminal hairs of tail tipped with black.
Dimensions of the type (measured in spirit before
skinning) :—
Head and body 168 mm. ; tail 141; hind foot 39; ear 14.
Skull: greatest length 40; basilar length 31; palate
length 16; length of upper molar series (excluding minute
anterior premolar) 6:2.
Hab. (of type). Capangombi, southern plateau of Angola.
Type. Male. B.M. no. 92.1. 9.6. Received in exchange
from the Lisbon Museum.
Two specimens from ‘ Angola,” collected by Mr. Monteiro,
and some imperfect skins from the Cunene River, collected
by C. J. Andersson, may be referred to this form.
25. Otomys trroratus, Bts.
3g. 29. Pungo Andongo.
9. 163. Braganza.
26. Tatera valida, Bocage.
g. 184,193. Braganza.
~@. 105, 125, 126, 127. Pungo Andongo.
27. Cricetomys Ansorge?, sp. n.
g. 389; 9. 18,22. Pungo Andongo.
dg. 211s 82212. Golunzo Alto:
Size even larger than in C. gambianus. General colour
drab-brown, paler than in true gambianus, darker than in the
southern form of that animal. Under surface of a similar
colour, but little paler than above, the throat and inguinal
region alone more whitish. Young specimens, however,
have their belly whitish. Cheeks paler than body, ‘ wood-
brown,” muzzle and orbital rings darker brown, an irregular
whitish patch at the base of the whiskers. Arms and legs
like body; metacarpals blackish brown mesially, digits and
outer edge of metacarpals whitish; ankles and metatarsals
blackish brown, toes lighter, but not conspicuously contrasted
white. ‘Tail black for its proximal, white for its terminal
half, the contrast more marked than is usual in gambianus.
Skull similar to that of C. gambianus, but larger throughout,
and with heavier molars.
Mammals from Northern Angola. 413
Dimensions of the type (measured in the flesh) :—
Head and body 400 mm. ; tail 469 ; hind foot 78; ear 47.
Skull: greatest length 82 ; basilar length 67; zygomatic
breadth 38 ; nasals 34% 11'8; interorbital breadth 12; brain-
case, breadth 26; palate length 40; diastema 25; palatal
foramina 8-2; length of upper molar series 12:1.
Typical locality. Pungo Andongo.
Type. Old male. B.M. no. 4. 4.9.91. Original number
39. Collected 9th June, 1903.
In its large size, unwhitened belly, and dark metacarpals
this huge rat differs from any of the forms of the widely
spread C. gambianus, and seems to represent a special
Angolan species. The two forms of the group, no doubt
synonymous with each other, from Landana described by
Rochebrune * are both far smaller and have their bellies “ albo-
cinereis.”
A comparison of the specimens of C. gambianus in the
Museum shows that the typical form occurs from the Gambia
down through the forest-region of West Africa to the Congo,
and eastwards to Monbuttu. It is chocolate-brown along
the dorsal area, paler on the sides, and with a sharply defined
white belly. Further south, from the lake-region to Portu-
guese South-east Africa, it is replaced by a paler form, which
may be called
Cricetomys gambianus viator, subsp. n.
Size and general characters as in Mus gambianus, but body-
colour much paler, the back ‘svood-brown,” scarcely darker
along the spine. Under surface white, not quite so sharply
defined as in gambianus. Tip of muzzle and orbital rings
dark brown; edges of upper lip white; cheeks like flanks.
Upper surface of hands white, the brown of the forearm
ending on the wrists. Centre of metatarsals dark brown,
‘the toes prominently contrasted white. ‘Tail half blackish,
half white, the two colours hardly so strongly contrasted as
in C. Ansorget,
Dimensions of the type (measured in skin) :—
Head and body (stretched) 415 mm.; tail 370; hind
foot 68; ear 44,
Skull: greatest length 73; basilar length 62; zygomatic
breadth 35; nasals 81x11; interorbital breadth 11:3; pala-
tal foramina 8°7 ; length of upper molar series 10-5.
* Cricetomys dissimilis and Mus tephrus, Bull. Soc. Philom, (7). ie.
pp. 86, 87 (1885).
414 Mr. O. Thomas on
Hab. (of type). Likangala, Nyasaland.
Type. Old male. B.M. no. 2. 1. 6. 83. Collected June
1901 and presented by Sir Alfred Sharpe, C.B.
28. Arvicanthis dorsalis griselda, subsp. n.
3.174; 9.175. Muene Coshi, Jinga Country.
Like the true southern A. dorsalis in all essential respects,
but the colour is paler throughout, with less ferruginous
suffusion ; sides of head and flanks pale lined greyish with
scarcely a tinge of buffy. Orbital rings and sides of muzzle
pale yellowish, not ferruginous. Belly white.
Molars rather smaller than in the typical subspecies.
Dimensions of type (measured in flesh) :—
Head and body 121 mm.; tail 185; hind foot 28; ear 14.
Skull: greatest length 31; basilar length 25; breadth of
brain-case 12°5 ; palatal foramina 6:1; length of upper molar
series 6°1; breadth of m' 2°1.
Type. Adult, but not old, female. B.M. no. 4. 4. 9. 95.
Original number 175. Collected 26th September, 1903.
The present is the furthest towards the north-west that
A, dorsalis has been recorded, and, considering the great
distance from the Cape, it is not surprising that there should
be a difference in colour worthy of subspecific recognition.
On the eastern side of Africa A. dorsalis goes slightly
farther north, but there, instead of being more pallid, the
colours are intensified, while the reduction in the size of the
molars is carried to anextreme. ‘This eastern form may be
called
Arvicanthis dorsalis rosalia, subsp. n.
Essential characters of true dorsalis, but the colours strong
and dark, a large proportion of the rump strong ferruginous ;
sides of muzzle, orbital rings, and ears rich rusty.
Skull small and narrow, the molars conspicuously weaker
than in the typical form.
Dimensions of the type :—
Head and body (in skin) 119 mm. ; hind foot (wet) 28;
ear (wet) 15.
Skull: back of interparietal to tip of nasals 31 ; zygomatic
breadth 14:2; interorbital breadth 4°4,; brain-case, breadth
12:7; palatal foramina 6°5 ; length of upper molar series 5:6 ;
breadth of m? 1:7.
Hab. Monda, Nguru Mountains, German East Africa.
Type. Adult female. B.M. no. 90. 6.8.28. Presented by
Kmin Pasha.
Mammals from Northern Angola. 415
29. Arvicanthis pulchellus, Gray.
. 63. Pungo Andongo.
- Lod, 1653 S150, 181,182; 186: “Braganza.
. 177. Marimha, Jinga Country.
Oy O4 OY
30. Pelomys campane, Huet.
od. 4. Ambaca.
S$. 39, 36, 118, 119; 9. 37,130. Pungo Andongo.
gd. 149,161. Braganza.
Type locality. Landana, Lower Congo.
31. Pelomys frater, sp. n.
6. 168; 2. 154,167. Braganaa.
A darker-bellied form than P. campane. Molars larger.
General colour above of the usual iridescent dark yellowish
olive; no dorsal stripe. Sides rather more buffy. Under
surface dirty greyish buffy, the hairs dark slaty for two thirds
their length, buffy at tips; line of demarcation on sides not
sharply defined, the upper and lower colours passing quite
gradually into each other. Head rather greyer than body ;
sides of muzzle and orbital rings not prominently buffy ; ears
dark brown, a ferruginous spot at their anterior bases.
Limbs like body ; upper surface of hands and feet grey, not
fulvous. ‘Tail shorter than in P. campane, black above, dull
whitish below.
Skull much as in P. campane, the palatal foramina rather
shorter and the bulle larger.
Incisors thick and powerful. Molars very broad and
heavy, conspicuously larger than in P. campane.
Dimensions of the type (measured in the flesh) :—
Head and body 139 mm. ; tail 136; hind foot 31; ear 20.
Skull: greatest length 32; basilarlength 25-7 ; zygomatic
breadth 15°5; nasals 11:7; interorbital breadth 4:7; breadth
of brain-case 14; diastema 8; palatal foramina 5-8; length
of upper molar series 6°8 ; breadth of m! 2°5.
Hab. Braganza.
Type. Male. B.M. no. 4.4. 9.107. Original number 168,
Collected 6th August, 1903.
It is interesting to find two forms of Pelomys inhabiting the
same region, but there can be no question as to the distinction
of P. frater from P. campane. Pousargues’s P. Dybowskit,
from French Congo, is a very much larger species than either
(hind foot, c. u. 38; molars 8°5 mm.).
416 Mr. O. Thomas on
32. Dasymys sp. (probably nudipes, Pet.).
?. 159. Braganza.
33. Ginomys (g. n.*) hypowanthus Anchietew, Bocage.
Mus Anchiete,, Bocage (the male only).
&. 24.98.98; 9.25. Pungo Andongo.
The “ Mus Anchiete” of Bocage is clearly a member of the
hypoxanthus group, but is separable from the Gaboon form
by its rather lighter colour, in which respect it approaches my
Gi. h. unyorét. From this latter it is distinguished by the
lesser extension of the rufous over the back and the less
wholly red feet.
With regard to the general ‘position of the hypovanthus
group, further consideration convinces me that the molars
are so peculiar that it ought not any longer to be included in
Mus, and I therefore suggest a special generic name for it.
A good account of its dentition, with figures, has been
given by Tullberg {, and in Bocage’s paper there is also a
photograph of the under aspect of the skull. The characters
of @nomys would be as follows :—
General structure as in Mus, but the molars very broad,
rounded, with peculiarly prominent cusps; the individual
cusps separated by deep antero-posterior grooves from each
other, so that the essential laminate structure of the molars is
lost. JZ? and m? each with a large antero-internal supple-
mentary cusp and small antero-external one. Z* with very
large antero-internal supplementary and main internal cusps,
but the external ones, both supplementary and main, almost
or quite obsolete.
34. Mus Bocaget, sp. n.
ao. 19,. 30,78, 86,128 5 2). 20 27, 45) 0. mee
Andongo.
A large pale brown rat, with white belly and feet; mamme
0O—2=4.
General colour pale brown, resulting from a mixture of
blackish and clay-colour; sides greyer; belly white, fairly
sharply defined, the hairs slaty grey at their bases only.
Head like body, orbital rings darker. ars of medium
length, brown. Outer side of limbs like body, inner like
* Gnomys, g.n. Type Mus hypoxanthus, Pucheran.
+ Ann. & Mag. Nat. Hist. (7) xii. p. 343 (1903).
{ N. Act. Upsala, (3) xvi. Art. xi. p. 26 (1893).
Mammals from Northern Angola. 417
belly ; upper surface of hands and feet pure white. Tail
about the length of the head and body, practically naked,
the few fine hairs about one scale in length ; scales coarse,
about nine rings to the centimetre ; colour uniformly brown.
Mamme 0—2=4, all close together near the vulva.
Skull long, well-ridged, the ridges not sharply divergent ;
palatal foramina long, rather narrow, reaching back to
the level of the first lamina of mm’. Bulle of medium size,
smaller than in I. Hinded and Thomasi, much larger than in
M. sebastianus.
Teeth rather light, the molars much narrower than the
palate between them.
Dimensions of the type (measured in the flesh) :—
Head and body 191 mm. ; tail 189; hind foot 35; ear 28.
Skull: greatest length 41; basilar length 32°25; zygo-
matic breadth 20; nasals 15:5; interorbital breadth 6;
breadth between ridges on parietals 13; diastema 11; pala-
tine foramina 8°7; length of bulla 7; length of upper molar
series 6:2.
Hab. Pungo Andongo. Alt. 1200 m.
Type. Male. B.M. no. 4. 4. 9.62. Original number 128.
Collected 13th September, 1903.
This fine species may be readily recognized by its size,
nearly naked large-scaled tail, white belly and feet, and
unusual mammary formula.
An example of it seems to have been the “ Femina: colori-
bus pallidioibus. Mammez quatuor inguinales ” of Bocage’s
Mus Anchietw, but the male and all other parts of the descrip-
tion refer to an Ginomys (see above).
I have great pleasure in dedicating this species to my friend
Prof. Barboza du Bocage, of Lisbon, to whom I am much
indebted for help, and in whose many papers almost the
whole of our knowledge of Angolan mammals is enshrined.
85. Mus avunculus, sp. n.
6.49. Pungo Andongo.
Like M/. angolensis, but larger, with white belly and more
hairy tail.
General colour above pale fawn-grey, about as in AZ, angol-
ensis, but the rump distinctly redder (dull “ochraceous buft”).
Under surface, from chin to anus, pure white, the hairs white
to their roots. Head clearer grey, without buffy suffusion.
Ears of medium size, grey. Upper surface of hands and feet
pure white. ‘ail distinctly ringed (ten rings to the centi-
metre), almost naked basally, the rings there obvious, but ter-
minally the hairs increase in length, hiding the scales on the
418 Mr. O. Thomas on
last inch, and forming a slight pencil at the tip, where they
are about 2 mm. in length ; colour pale brown, rather lighter
proximally below. Mamme unknown.
Skull very like that of IZ angolensis, but larger; anterior
edge of zygomatic plate slightly concave.
Dimensions of the type (measured in skin) :—
Head and body 136 mm.; tail 176; hind foot 28; ear 19.
Skull: greatest length 34; basilar length 25°5; nasals15;
interorbital breadth 4°6 ; diastema 8°5; palatal foramina TOR
length of upper molar series 5:2.
flab. Pungo Andongo. Alt. 1200 m.
Type. Old male. B.M. no. 4. 4. 9. 67. Original number
49. Collected 14th June, 1903.
This rat looks at first sight like a diminutive relative of
Mus Bocaget, but it would seem on the whole more related to
M. angolensis, from which it differs by its reddish rump,
white belly, more hairy tail, and longer feet. If this view of
its affinities is correct, its mammary formula should prove to
be 8—2=10.
36. Mus angolensis, Boc.
cg. 40,015 9. 114,117, | Puneo Andongo:
This is the Angolan representative of the widely distributed
rat with 3—2=10 mamme, otherwise so like the multi-
mammate form. It appears to lave, however, broader poste-
rior nares than the latter.
37, Mus sp. (multimammate).
3. 79,103, 106,116; 9. 67,111,115. Pungo Andongo,
38. Mus arborarius, Peters.
dé. 107,121; 9. 90:. Pungo Andongo,
39. Mus carillus, sp. n.
3. 33, 50, 61,82,118; 9. 26,65, 85. Pungo Andongo.
A small buffy mouse, with long tail, similar to AZ. Adlend.
Mamme 1—2=6,
Size small, form delicate, with slender feet and long thin
tail. Fur soft and fine, hairs of back about 6-7 mm. in
length. General colour above buffy fawn, varying very
inuch in tone and brightness according to age and state of
development, some of the younger specimens near “ cinna-
mon,” older ones almost ‘‘ochraceous.” Under surface greyish
Mammals from Northern Angola. 419
white, the hairs slaty for their basal two thirds, white ter-
minally. Outer side of limbs like sides, inner side like belly ;
hands white from wrists; ankles inconspicuously brown,
upperside of feet white; filth toe reaching to the end of the
second phalanx of the fourth. Tail long, slender, thinly and
fairly haired, scarcely pencilled at end, uniformly pale brown ;
rings of scales very fine, about sixteen or seventeen to the
centimetre. Mamme 1—2=6.
Skull low and broad, with a large brain-case and small
muzzle ; supraorbital edges square, but not markedly beaded,
the faint ridges disappearing halfway across the parietals ;
palatal foramina not very widely open, reaching back to the
level of the front of m'; palate ending squarely just behind
m® ; bullee small.
Dimensions of the type (measured in the flesh) :—
Head and body 96 mm.; tail 146 ; hind foot 20 ; ear 16.
Skull: greatest length 26; basilar length 20; zygomatic
breadth 12°5; nasals 9; interorbital breadth 4°5; breadth of
brain-case 11:2; height of brain-case 7°5; palate length 11;
diastema 6°6 ; palatal foramina 4:7 ; length of upper molar
series 40.
Hab. Pungo Andongo. Alt. 1200 m.
Type. Old female. B.M. no. 4. 4.9. 74. Original num-
ber 65. Collected 20th June, 1903.
Even apart from the number of its mamme this pretty
mouse is readily distinguishable from Mus Alleni, the only
species with which it could be compared, by its much paler
colour and its wholly white feet.
40. Lophuromys sikapust, Temm.
do. 162. Braganza.
41. Dendromys sp.
3. 213. Golungo Alto.
A striped species whose identity with the southern D. meso-
melas and melanotis I am at present unable either to affirm or
deny.
42. Steatomys Bocagei, Thos.
3. 133, 185, 187, 164, 165; 29. 132,155. Braganza.
43. Georychus Mechowi, Peters.
3. 152, 153, 170,178; 9. 169. Braganza.
420 On Mammals from Northern Angola.
44, Georychus Bocagei, de Wint.
gd. 142, 151, 160, 189, 190, 191. Braganza.
os AD.., Ambaca:
g. 129. Pungo Andongo.
45. Lepus angolensis, sp. n.
Lepus ochropus, Bocage, nec Wagner.
OF 3 ls Lie Abaca.
9. 15. Pungo Andongo.
A dark strongly coloured species, with rufous neck ; enamel
foldings of incisors peculiar.
General colour above dark, a dark clay-colour grizzled with
blackish, the hairs with a subterminal band of dark buffy and
black tips; sides rather paler. Centre of face dark lined
buffy, a white frontal spot generally present. Sides of muzzle
whitish and a narrow orbital ring of the same colour; an
indistinct patch below the front of the eye blackish. Nape
bright rufous, near “ tawny ochraceous” of Ridgway. Lars
of medium length; anterior part of external surface dark
lined greyish; the fringing hairs dark buffy ; tips edged with
black ; outer margin white basally, becoming buffy terminally,
Chin and interramia white, throat dull buffy; belly white,
not sharply defined laterally. Fore limbs dull cinnamon, a
narrow line on the inner side of the forearms white. Hind
limbs similar, their inner surfaces.more broadly white. Tail
of medium length, black above, white on sides and below.
Skull in its general proportions not unlike that of Z. Whytet,
Thos., of medium length, stoutly built, without noticeable
peculiarities.
Incisors with the involution of the enamel about as in
L. Whytei*, the groove practically filled up with cement.
Section of upper incisors of Lepus angolensis.
But, in addition to the main involution, there is a further and
peculiar complexity in the presence of a fine thread (as seen
in section), apparently of enamel, passing backwards and
* Figured by Forsyth Major, Tr. Linn, Soc., Zool. vii. p. 468, figs, xi
& xiii. (1899).
Mr. H. Schwann on Felis ocreata. 421
outwards from the middle of the antero-internal peninsula
towards the centre of the main dentine area of the tooth,
dying away about halfway across to the hinder margin, This
additional complexity of the incisive section has not been
hitherto noticed in any hare.
Dimensions of the type (measured in the flesh) :—
Head and body 390 mm.; tail 90; hind foot 115; ear 115.
Skull: back of parietals to tip of nasals 78; basilar suture
to henselion 55; zygomatic breadth 39; nasals, length
diagonally 34, greatest breadth 18; interorbital breadth 20;
diastema 23; breadth of palatal bridge 7; palatal foramina
21x9.
Hab. (of type). Ambaca. Alt. 800 m.
Type. Adult female. B.M. no. 4. 4. 9. 140. Original
number 7. Collected 29th April, 1903.
The Angolan hare was referred by Prof. Bocage to Lepus
ochropus, Wagn., but that is the yellow-naped High Veldt
representative of LZ. capensis*. Jentink’s DL, sale, from
Mossamedes, is a far paler form, with much shorter tail.
Probably LZ. angolensis is most nearly allied to the Zambe-
sian L. Whytei, but differs from that as from all other species
by the unusual complexity of its upper incisors.
46. Procavia Bocaget, Gray.
@. 51 (imm.). Pungo Andongo.
XLIX.—On Felis ocreata, better known as Felis caligata, and
its Subspecies. By HAROLD SCHWANN.
Tyr first account of this cat appears in Bruce’s ‘Travels
to Discover the Source of the Nile’ +, under the name of the
“ Booted Lynx,” and, with the exception of the exaggeration
of the ear-tufts in the plate, appears to be a very accurate
description.
In 1791 E. W. Cuhn published at Leipzig a German
translation of the ‘ Travels,’ with a zoological appendix by
J. F. Gmelin, where the latter distinctly gives the name of
Felis ocreata to Bruce’s specimen.
F. ocreata therefore stands as being the earliest technical
name of the species.
* Cf. Ann. & Mag. Nat. Hist, (7) xii. p. 344 (1903).
+ Vol. v. p. 146 (1790).
{ Anh. Bruce Reisen, Gmel. p. 27 (1791).
Ann. & Mag. N. Hist. Ser. 7. Vol. xii. Pics
422 Mr. H. Schwann on Felis ocreata.
Mr. W. E. de Winton, in Anderson’s ‘ Zoology of Egypt’ *,
has taken Meyer’s Felis lybicat as representing Bruce’s
“ Booted Lynx,” not having noticed Gmelin’s earlier name.
It seems, however, very probable that Meyer’s F. lybica is
applicable to some form of caracal, as the first part of the
description he quotes from Forster’s translation of Buffon
(the original describer) runs as follows :—‘‘ Corpore rufo,
auriculis albis nigrobarbatis.”
The names that have been applied to this group at different
times are given below, with the locality where each type was
collected, so far as this can be ascertained with any exactness :—
“ Booted Lynx,” Bruce, Travels Source of the Nile, vol. v. p. 146 (1790).
—Ras el Feel, Abyssinia.
Felis ocreata, Gmelin, Anh. Bruce, Reisen (Rinteln und Leipzig), vol. ii.
p27 (yon):
Felis cafra, Desm. Encycl. Méth., Mamm, Suppl. p. 540 (1822).—
“ Caffraria.”
Felis caligata, Temm. Monogr, Mamm. no, 4, vol. i. p. 128, 1824 (1827)
(ex Bruce).
Felis maniculata, Temm, op. ett. p. 128.—Ambukol, on the Nile.
Felis Riippellt, Schinz, Cuv. Thier. vol. iv. p. 509 (1825).—Dongola.
Felis bubastis and. F. dongolane (nom. nud.), Hemp. & Ehrenb. Symb.
Phys. dec. ii. text to pl. xvii. (1882).
Felis pulchella, Gray, Charlesw. Mag. Nat. Hist. i. D 577 (1857) ).—Kegypt.
Felis margarita, Loche, liev. et Mag. Zool. p. 49 (1858).—N’gouca,
Algerian Sahara.
Felis cr istata, Lataste, Faune des vere de Barbarie, p. 104 (1885),—
Haidra.
It appears very probable that /. pulchella ought to« be
considered a synonym of /’. maniculata, Temm., but the
British Museum does not at present possess sufficient North-
African material to settle the question definitely.
I regard the following new forms as subspecies partly
hecause their differences from Felis ocreata are not marked
enough to warrant specific distinction, and also on account
of the great convenience the use of trinomial nomenclature is
in linking together the members of a widely distributed
group.
Felis ocreata rubida, subsp. n.
Resembles F. 0. ocreata in general proportions, but is
strongly suffused with fulvous on the head, body, and feet.
General colour of the upper surface “ hair-brown,” the
sie erg eC Es
+ Meyer, ‘Syst. Zool. Entd. Neuholland u. Afr.’ p. 101 (1793),
t Forster, ‘Ueberf. v. Butt. Naturgesch. der vierfiissigen ‘Thiere,’ B. vi.
p. 318 (1780).
Mr. H. Schwann on Felis ocreata. 423
median line strongly fulvous, pencilled with black ; flanks
covered with irregular brown spots. Individual hairs of back
about 15 mm. in length ; their basal third drab, middle third
cinnamon-colour, subterminal ring dark brown, almost black,
tip buffy. Muzzle, upper lip, ears, and sides of throat bright
fulvous ; a white patch above and below the eyes, nape dark
brown ; four indistinct brown lines extending from forehead to
shoulders ; interramia pure white, shading into dull buffy on
the throat and chest ; belly cinnamon-colour, marked with
indistinct black spots ; inguinal region buffy yellow. Upper
surface of fore and hind limbs light brown, ringed with
several indistinct brown bands; forearms partially black ;
feet fulvous above, black beneath ; tail coloured like back,
tip black, three or four subterminal black rings.
Dimensions of the type (from the dried skin) :—
Head and body 575mm. ; tail 286; hind foot 127; ear 54.
Skull: basilar suture to nasion 60°5; breadth of brain-
case 44°2 ; temporal breadth 30°6 ; anteorbital breadth 14:0;
zygomatic breadth 62°0 ; outer length of upper carnassial 10°7 ;
ereatest length of auditory bulla 22°0.
Hab, Monbuttu.
Type. Male. B.M._ no. 87. 12. 1. 6. Collected and
presented by Dr. Emin Pasha.
A young specimen obtained by Dr. Emin from the same
locality has the characteristic spots on the flanks and the
fulvous coloration on the median line, but is of a rather lighter
colour throughout.
Felis ocreata Mellandi, subsp. n.
Very uniformly coloured, no spots or bands on the back
and sides.
General colour of the upper surface greyish buff, darker on
the median line. Individual hairs of back about 35 mm. in
length ; basal two thirds dull buffy yellow ; subterminal ring
black; tip light grey. Under surface creamy buff; the hairs
erey basally, middle third buff, terminal third creamy yellow.
Nose and ears bright yellowish; cheeks and interramia light
yellow, almost white; forehead and nape darker than back,
the individual hairs black, with grey tips. Upper surface of
fore and hind limbs coloured like back; under surface black,
speckled with grey.
The two specimens of this subspecies in the British
Museum are incomplete as to their tails, so it is impossible
to say whether the usual black tip and subterminal rings
are present until more material is obtained. The tail (as
29*
AQA4 Mr. H. Schwann on Felis ocreata.
- much as is preserved) is coloured like the median line of the
back, rather darker than the flanks.
Dimensions of the type (from the dried skin) :—
Head and body 210 mm.; ear 48.
Skull absent in both specimens.
Hab. Mpika, North-east Rhodesia.
Type. B.M. no. 4. 3. 11. 2. Collected and presented by
F. H. Melland, Esq.
Ihave much pleasure in naming this cat after Mr. Melland,
who has collected a number of specimens for the National
Museum in the country round Mpika.
This subspecies may be readily distinguished by the sharp
contrast between the bright yellow of the ears and the rest
of the body as well as the entire absence of any markings on
the dorsal area.
A specimen collected by Mr. Alfred Sharpe in 1893 * at
Lake Mweru appears to be referable to Mellandt.
Felis ocreata uganda, subsp. n.
Similar to 7. 0. ocreata, but darker throughout.
General colour above yellowish grey, lighter on the flanks ;
median line of the back conspicuously darker, fulvous to dark
brown; flanks transversely banded with indistinct fulvous
stripes from ten to fifteen in number. Underfur of back about
15 mm. in length, proximal half smoke-grey, light buffy yellow
distally ; long hairs about 25 mm. in length, black, with white
subterminal ring and black tip. Under surface “ creamy
buff,’ covered irregularly with brown or blackish spots,
Muzzle, upper lips, and a patch above and below the eyes
strongly fulvous ; a line extending from the posterior margin
of the orbit to the middle of the cheek dark brown; edge of
the lips, lower part of the cheek, and a patch from muzzle
to eyebrows yellowish white; forehead and nape darker
than the back, in well-marked specimens nearly black ; ears
bright rufous, covered internally with long white hairs,
ear-tufts black ; interramia and throat white, with one or two
transverse buffy yellow bands; inguinal region thickly
covered with long buffy hair. Upper surface of fore and hind
limbs coloured like back, with several indistinct dark bands ;
feet bright buffy above, black below. ‘Tail coloured like
back or greyer; two or three black subterminal rings ; tip
black.
Dimensions of the type (taken in the flesh) :—
Head and body 584mm. ; tail 341; hind foot 181; ear 58.
* P.Z. S, 1893, p. 723.
Mr. H. Schwann on Felis ocreata. 425
Skull.
Male (type). Female.
mm. mun.
Greatest length...... tanh tas ee ate 103°0 92-0
Prasat LEN Wess. erat vers pg kaka waite aes 88:0 785
FAY EOWA IG DECAU CH ate crclsid nde nese yee 73° 63°2
PICCOR DIE BECAO LIM Bice ncilalc.’S a:5/5-S0; mare's ya 16°5 16-0
Remmporal bresdth.. faqs... ¢<0'% seats os 01s 31-2 35'6
Aral Case PReaOblir.: decfced «elo we «meacble o0,« 45°5 45:0
Greatest lencth of bulla ...05...2000 000s 24:0 23:0
Outer length of upper carnassial.......... 11:0 11:0
Hab. Mulema, Uganda.
Type. Male. B:M. no. 3: 11. 7. 8. Alt. 5000 feet:
Collected by Mr. W.G. Doggett and presented by Col. Delmé
Radcliffe.
The comparative skull-measurements given above serve
very well to show the difference in size between the sexes.
‘The specimens from which they were taken were both fully
adult and obtained in the same locality.
The colour of the female is slightly lighter throughout,
agreeing in this respect with a specimen obtained by
Capt. Speke at ‘ Memissa.”
Felis ocreata cafra, Desm.*
Mr. W. E. de Winton, in Anderson’s ‘ Zoology of Egypt’ fT,
decided that it was necessary to adopt the earlier name t of
obscura instead of cafra for the South-African race of Felis
ocreata, although the name was based on a melanistic specimen.
A comparison of the two descriptions with the British
Museum’s fine series of South-African skins seems to suggest
that after all Desmarest’s I’. obscura § may be nothing more
than a melanistic specimen of the domestic cat. It may be
noticed that the British Museum specimens do not have the
“ bandes transversales entiérement noires et trés-nombreuses,”’
nor is the species so small as the domestic cat, as F’. obscura
is said to be.
It appears, therefore, so doubtful whether /” obscura is really
referable to this species that I see no necessity at present for
altering the more suitable and better known name of ca/ra.
The British Museum does not at present possess sufficient
North-African material for me to decide detinitely as to the
status of ’. margarita, Loche, and F’. cristata, Lataste.
* Encycl. Méth., Mamm., Suppl. 1822, p. 540.
qe 74ay
{ Encycl. Méth., Mamm. 1820, p. 230. f
§ See Dict. des Sci. nat., F. Cuy., tom. viii. p. 222, for original
description.
426 Dr. A. G. Butler on certain African
A synopsis of the new forms described above is added to
assist in the identification of individual members of this
difficult group :—
A. No fulvous suffusion on the sides, no spots on the
flanks.
a. Underfur on median line of back cinnamron-colour,
forehead and nape not darker than back ...... F’. 0, ocreata.
b. Underfur on median line dark brown or black,
forehead and nape darker than back.
a’. Forearms conspicuously ringed with black,
underside of forearms deep black all over.... F. 0. cafra.
b'. Forearms inconspicuously ringed, underside of
forearms partially black.
a’, General colour pale, ears yellowish........ F. 0. Mellandi.
b''. General colour darker, ears rufous ........ F. 0. ugande.
B. Sides and limbs suffused with fulvous, well-marked
brown spois’on the TAM. is ce ct nee ae since F. 0. rubida.
L.—On certain African Butterflies of the Subfamily
Pierine. By Artuur G. Butuer, Ph.D., F.L.8., &e.
I THINK every true naturalist will agree with me that fair
criticism is valuable as a stimulus, and has the effect of
making a good workman exert himself to avoid error as much
as possible in his subsequent work. When, however, a man
has spared no pains to arrive at the exact truth, has built up
his facts brick by brick, until the edifice seems to be com-
plete, and another workman, with all the facts before him,
misrepresents them, it seems only right to expose the unfair-
ness of such criticism.
In a paper by Prof. Aurivillius published in the Upsala
‘Nya Tidnings Aktiebolag’ last year, and entitled ‘ Results
of the Swedish Zoological Expedition to Egypt and the
White Nile, 1901, under the direction of L. A. Jiagerskiéld.
—No. 8,” the author records two forms of Beleno’s under the
names Preris gidica, God., var. Westwood’, Wallengr., and
Pieris gidica, God., var. (?) abyssinica, Lucas ; and he ob-
serves, ‘‘It is very remarkable that Westwood also was taken
in the dry season at nearly the same time as abyssinica.
The relation between P. Westwoodi and abyssinica has been
the subject of much discussion, and is not yet sufficiently
cleared up. Butler says in 1894 (Proc. Zool. Soc. 1894,
p- 579), ‘Lam quite satisfied that B. gidica and B. abyssinica
cannot be regarded as distinct species’; and in 1898 (Trans.
Ent. Soc. London, 1898, p. 436), ‘I may begin by stating
Butterflies of the Subfamily Pierinee. 427
emphatically that gidica is not the wet-season form of
abyssinica.”
The above statement does give the impression, whether
intended or not, that in 1898 I flatly contradicted the state-
ment made by myself in 1894; but Prof. Aurivillius, with
both papers before him, is perfectly well aware that the
B. gidica of the first and second papers were entirely different
species or forms.
In 1894 we knew B. gidica from description only, and it
was supposed by all lepidopterists to be identical with the
B. Westwood? of Wallengren; but Godart’s type came into
the possession of, I believe, the Edinburgh Museum, was
brought to the British Museum for comparison, and thus the
fact that it was quite distinct from B. Westwoodi (=B. gidica
auct. plur.) was made evident.
In 1898, in the very paper to which Prof. Aurivillius
refers as evidence of the instability of my emphatic utterances,
I described the true .B. gidica as explanation of the very
sentence quoted, only part of which, moreover, was quoted,
since to quote the whole would have made the misrepresen-
tation of my assumed change of front evident: what I added
is, ‘‘ Furthermore, there are two South-African species of the
group, easily separated by anyone who has an eye for form
and pattern ” ; and I then proceeded to describe the differences
between the typical 2B. gidica and the form previously
regarded as that species by lepidopterists generally.
But, to make the point still more unmistakable, I in the
same paper described the seasonal forms both of B. abyssinica
and B. Westwoodi, showing that they are not, as I formerly
supposed, mere seasonal phases of one species, but that the
wet phase of each form is well marked, and indicates at least
the local distinctness of the southern and northern represen-
tatives of this type.
Now, to examine Prof. Aurivillius’s statement in detail.
It is not very remarkable that dry and wet phases should
both occur during the dry season. I have repeatedly shown
that, although the dry phase of a species is prevalent in the
dry season, examples of the wet phase are frequently present.
We do not know, and can only surmise, the cause of this fact :
it is possible that the position of a chrysalis near to or far
from the earth may have some effect in determining the
character of the developing butterfly ; in heavy dews it is
conceivable that the chrysalis near the surface of the earth
might be more affected by the moisture than if situated at
some height above the ground.
Again, I have shown that in very dry countries a species
428 On African Butterflies of the Subfamily Pierine.
_ will frequently develop all the phases characteristic of the
seasons simultaneously. Prof. Aurivillius cannot understand
this; therefore he says of Yeracolus daira:—‘It is very
peculiar to find this form, which is coloured like a summer
form, flying in the middle of the dry season together with
highly developed dry-season forms of other species. I there-
fore do not think that 7. nouwna, Lucas, is really a dry-season
form of daira.” If the Professor had paid more attention to
my argument—that the seasonal phases of species are only
variations formerly coexistent which have become more or
less seasonally fixed—there would be nothing peculiar to him
in the existence of a wet phase in the dry season, so long as
it was not as abundant then as in the wet season ; nor would
he have any reason for coming to the conclusion, on such
evidence, that J. nouna could hardly be the dry phase of
T. daira.
In the second place, I do not agree that the relation between
B. Westwoodi and abyssinica has not been cleared up. I
consider that, as I have described the seasonal phases of both,
the only question between lepidopterists is as to whether they
shall be called species or local forms—a question of absolute
unimportance, which can never be cleared up so long as
naturalists hold different views as to what constitutes a
species.
In the same page upon which Prof. Aurivillius makes the
remarks above discussed he describes and figures a very pretty
little species of Z/erpeenia, to which he gives the unnecessarily
descriptive name “ Herpania eriphia, God., var. hib, extrema
stramtinea, n. var.” Now, in the first place, it is not Herpenia
eriphia at all, the dry phase of which barely differs from the
wet, nor is it /7. melanarge, the dry phase of 7. cterata (which
1 suspect is the species recognized by Prof. Aurivillius as
nyasse, Lanz), but it is my LH. lactecpennis, described from
Abyssinia, and, I believe, sunk by Aurivillius as a synonym
of H. eriphia, probably because my friend Trimen, in his
‘South African Butterflies, vol. iii. p. 78, says he should
regard J. melanarge, judging from the description, as the
same as var. a (the dry phase of H. eriphia), and lacteipennis
from Abyssinia, notwithstanding its unusually small size, as
referable to the same variety, if it were not for the description
of the hind wings. Mr. Trimen had then not seen the types
of either species or local representative (whichever one may
please to call these closely related forms); and, therefore,
when the Professor was in London he should have carefully
examined them himself, and so at least saved himself from
perpetrating so terrible a synonym fora pretty little butterfly
Notes on Phasmide in the British Museum. 429
as that quoted above. It is a long time, since 1876, for my
species to have remained unknown to one of the chief workers
at the lepidopterous fauna of the dark continent; in twenty-
seven years surely he should have gained some idea of the
identity of a species the type of which he might have
examined at the Museum on more than one fairly long visit
to London.
LI. — Notes on Phasmide in the Collection of the British
Museum (Natural History), South Kensington, with Descrip-
tions of new Genera and Species—No. Il. By W. F.
Kirsy, F.L.8., F.E.S.
Subfam. I]. Bacrercrrmz.
I am obliged to form a new subfamily for my genus Bac-
tricia (=Scaphegyna, Karsch), which agrees with the
Lonchodinee in its long antennze and in the short median
segment, but differs entirely in the large incurved cerci of
the male and in the long operculum of the female.
The two known species are from Africa, and I now add
one from Singapore. (By some error the name of this sub-
family has been given as Bacteriine in the list on p. 872
antea.)
Genus Bacrricta, Kirb.
Bactricia Ridley?, sp. n.
Male.—Greenish brown; head short, narrowed behind, and
with two compressed obtuse horns between the eyes; space
between the horns and the antenne, sides of head, (probably)
the propectus, and a lateral streak below the median segment
white. Antenne and legs long and slender, the latter nearly
straight, and unarmed except for a sharp, flattened, curved
tooth near the base of the middle femora beneath. Median
segment half as long again as broad; abdominal segments
2-6 about three times as long as the median segment, the
seventh about twice as long; segments 8 and 9 about as
long, tenth rather shorter, concave at the extremity; cerci
compressed, almost spatulate, incurved and crossed ; oper-
culum extending as far as the ninth abdominal segment.
430 Mr. W. F. Kirby—WNotes on Phasmidee
Dimensions.
mm
one Kconponistrauyys sets tates Clo eo cg Foe 45)
pp CAPILIS vane eevee ewes ec ern se ce clas 4
oy, PROMOTE sks Me tlae s cee ae ee eee 5
opt \ MMB OMLOGE: [pet aia ARLE Pa le eieie eet Soe Ae)
» Mmetanoti, cum segm.med. .........: 25
pet, OPM ICC.) eto e iota eyaie alton ieisasya) ayers Saiode 8 abs}
She USNS CHIN ease oo means Sapeadeie carters 40
Oo
si es 6c! Cred rear AO ouch oe
+ 7) PRPOR Gs sede ents enone Snleata6 a Al
Tlab. Singapore (Ridley).
Allied to B. trophinus, Westw., from Natal, but in the
male of that species the horns are much more slender and
pointed, and the middle femora are unarmed.
Subfam. III. Bacrztrvz.
Clitumnide et Baciliide, Brunner.
The very short median segment and the large incurved
and frequently crossing cerci of the males will provisionally
bring together a series of apterous Old-World species which
agree with the American Diaphomerine in most respects,
but differ in the shortness of their antenne. With Brunner’s
Clitumnide I associate his Bacillide, considering them too
closely related to Phthoa &c. to be separated from them,
notwithstanding the more or less distinct excavation at the
end of the tibiae, which will, perhaps, prove to be a less
important character than has been supposed. It is not nearly
so distinctly marked in some genera of Phasmide as in others.
Another reason for removing the Clitumnide from the
position in which they were placed by Brunner is that they
come between the Necrosciine and Acrophylline, winged
Old-W orld subfamilies which agree in the shape of the median
segment.
Subfam. LV. Drarvouerinsz.
Bacunculide, pt., Brunner.
I employ this name for a series of American genera allied
to the Lonchodine by the very short and well-marked median
segment and to the Bacilline by the large and generally
incurved cerci of the males. Sacunculus and the genera
following it in Brunner’s arrangement appear to me to be
more closely related to the Bacteriine.
in the British Museum. 431
Genus CAULONIA, Stal.
|| Ceroys, Sauss. (nec Serv.).
A series of utterly discordant species have been placed in
this genus, the type of which is Caulonia bifolia, Stal, allied
to Ceroys rhabdota, Westw.; but I have not sufficient
material available to justify me in attempting to break it into
natural genera. The genera including spiny Phasmide are
in greater need of revision than any others of the family.
However, judging by the description, I think that Paro-
brimus, Scudd., is probably allied to Caulonia, and that
Ceroys laciniatus, Westw., may be referable to it.
Subfam. V. Bacrerinz.
Bacunculide, pt., and Bacteride, pt., Brunner.
I employ this name provisionally for a series of apterous
American genera in which the median segment is either as
long as the metanotum or else, especially in the males, so
closely fused with it that no division is visible. The genera
Bacunculus, Burm., and Dyme, Calynda, Bostra, and
Clonistria of Stal, included by Brunner in his Bacunculidse,
will fall into the present subfamily, and also the following
genera, included by Brunner in his Bacteridees :—Phibalosoma,
Gray; Phanocles, Stal; and Bacteria, Latr. I include
Phibalosoma (and some allied American genera not mentioned
by Brunner) in this subfamily, although they have winged
males, because they agree too closely with Phanocles and
Bacteria to be referred to a distinct family. I also include
the genera Bactridium, Sauss., and Abrachia, Kirb., though
they are not very closely allied to the other genera ; but I
cannot find a better place for them. Adrachia has no trian-
gular spaces at the end of the tibie beneath, as I have
erroneously stated, but a very large one at the end of the
middle femora, the caring of which project at the end on each,
side in a strong spine.
Genus TeRsoMIA, nov.
Antennee only one third of the length of the front femora,
23-jointed ; scape flattened, twice as long as broad; second
joint rather longer than broad, flattened, narrower than the
scape, the rest slender, linear ; third joint the longest, three
times as long as broad, the fourth scarcely longer than broad,
the rest gradually increasing in length to beyond the middle
and then gradualiy shortening to the extremity. Head
432 Mr. W. F. Kirby—Notes on Phasmide
considerably longer than broad, narrowed behind, with a
pair of short, stout, very obtuse horns on the vertex between
the eyes. Legs and body long, slender, smooth, legs nearly
straight; tibiz carinated to the extremities, terminal spines
of the front femora and outer side of the middle femora
very slightly marked, those on the inner side of the middle
femora and on both sides of the hind femora more con-
spicuous; first joint of tarsi at least as long as all the rest
together ; median segment fused with the metanotum, longer
than broad ; segments 2-7 of the abdomen from two to four
times longer than broad; three terminal segments slightly
longer than broad, carinated above, terminating in a very
long operculum, trifid at the extremity.
Appears to be allied to Clonistria, Stal, but with much
shorter antenne and very long operculum.
Tersomia brasiliensis, sp. n.
Female.—Light brown, legs pubescent; meso- and meta-
notum above with a double yellowish line, head and pronotum
less distinctly streaked and dotted with yellowish.
Dimensions.
mm.
LE CTsteR dopa HAN te mo oes ao aewos ac « mol
by ho MRRIK UC UATN UP UNITT as crs lei fa ee a nlladeiaieie 22 SG
i SACADUUS U2 eae highs racoiera 5c 2)
jy ME PEONOU o.ic)< he eare sie chek teens eae 5
5). MAMESOMOEL che fleas Ga Chale aese he dee Oe
», Metanoti, cum segm.med, .,.. 26
3) pROpeICUlL Gate heer eer Piet a eG
TOs ATG i teres tere naieaenet: aie ses -. 4
TMC Cs AE Rial che eae ain. Gade hae e 3l
POStY: ek. ke uesmce Maeelah ot eee
” ”
” ”
Hab. Iguarassu, Brazil (Lidley).
Subfam. VI. Paryeavisrriinz.
Lonchodide, pt., et Bacteride, pt., Brunner. -
I propose this subfamily to include the Eastern genera
Phryganistria, Sadyattes, and Pharnacta of Stal, and Ttra-
choides of Brunner. The males are winged, except in
Phryganistria. Phryganistria is placed by Brunner in the
Lonchodidee, but its real affinities appear to be with the other
genera, which he places in his Bacteride. ‘They agree with
this group, as I have restricted it, in the form of the median
segment, and I think it best to treat them as an independent
subfamily.
an the British Museum. 433
With these may perhaps be associated some of the species
placed by Westwood in his genus Lopaphus, which, except
for the possession of wings, much resemble Lonchodinee.
Genus LoPpAPHUS, Westww.
Lopaphus, Westw. Cat. Phasm. p. 99 (1859); Wood-Mason, Journ.
Asiatic Soe. Bengal, xlvi. p. 347 (1877).
Phasma, group 15, Haan, Temminck, Verhandel., Orth. p. 125 (1842).
As Westwood’s genus corresponds to De Haan’s group 15,
one of the four species included in that group by De Haan
(Bojet, brachypterum, Macklottii, and galacpterum, H.) must
be regarded as the type. But Wood-Mason (supra) enume-
rates a series of species as belonging to Lopaphus, among
which brachypterum is the only one of De Haan’s included ;
and this consequently becomes the type.
However, the other species placed by Wood-Mason in
Lopaphus are not congeneric, but belong to Cundaules, Stal,
and other genera. L. brachypterus is probably allied to the
following genus.
Genus PH ANOPHAROS, nov.
Antenne nearly as long as the front legs and composed of
a great number of joints; head with 4 or 5 tubercles behind,
and about as long as the pronotum; mesonotum nearly one
third of the whole length of the body ; median segment very
long, fully half as long as the metanotum; legs very long;
front legs longest, middle legs shortest ; first joint of front
tarsi longer than the remaining joints together, and with a
lamellated crest at the extremity; all the tibie with two
spines towards the extremity on each lower carina; hind
tibise with a small basal lamina beneath on the inner side ;
tegmina squamiform, Wings hardly as long as the median
segment.
Type, Lopaphus struthioneus, Westw., from Singapore and
Penang.
The three specimens of this genus in the Museum probably
represent two species ; but it will be better to wait for a longer
series before differentiating them.
Subfam. VII. Pazorurmz.
I have no observations to make on this subfamily,
434 Mr. W. F. Kirby—Notes on Phasmidee
Subfam. VIII. Nzcroscrr 2.
Genus Sosrsia, Stal.
Sosibia peninsularis, sp. n.
Female. — Brown, thickly dotted with grey; antenna
black, ringed here and there with yellowish towards the
extremity; front sloping above the antennze, this portion
bordered behind by a curved row of a few small tubercles,
one of which on each side is black and more conspicuous than
the others. The head is covered with short black spines,
arranged in about four rows on each side of the median line ;
the row nearest the median line on each side is more regular
than the others, and terminates above the frontal depression in
a single central spine ; towards the margins are some black
tubercles among the spines. The thorax is strongly tuber-
culate, and the prothorax bears a double row of black spines,
slightly converging hindwards, the intermediate ones longer
than the others, and in front of the mesothorax are two short
spines on each side close together. The front legs are testa-
ceous, banded with brown, and the front femora expanded
and flattened ; the middle and hind legs are yellowish, with
the extremities of the femora and tibiz and at least the last
joint of the tarsi black. ‘The tegmina are brown, slightly
bordered with yellowish, and convex ; the costal area of the
wings is light brown, varied with grey, and the membranous
part is brown and subhyaline. ‘The cerci are short and very
thick, especially towards the extremity.
Dimensions.
mm
(sone. COnpOTMS sy ens. oo = oii me nicer 81
» capitis ........64. ateceinis aiete ae a
By) PLOMOE potter Aprons 3 4
apf RCSONOl i, a. dete eters leeee oil 12
5, Mmetanoti, cum segm. med. 123
Pe pins Chines Ai atic BO OS DOID 404 123
“4 . med. peer aaa Otani: Aas 10
y ie SU Reon te son ans 4 os so) 6
ap) PL CEMIICON, ee vetareinie eh ceed eRe a
JPG oi) Evo separ actsia Brodie < en ees 115
This species is allied to S. n/grispina, Stal, and S. curtpes,
Westw. It may be the female of S. esacus, Westwood, but it
would be unsafe to put them together without evidence.
Hab. Penang (Flower).
Or
in the British Museum. 43
Genus CaALvIsIA, Stal.
Calvisia maculata, sp. n.
Female.—Testaceous (green when alive?), varied with
blackish. Head longer than broad; occiput convex, front
sloping and slightly excavated as far as the base of the an-
tenne ; a blackish band runs below the eyes obliquely upwards
to the back of the head, and there is a shorter one above it
running backwards from the eye, interrupted before reaching
a transverse black mark at the back of the occiput. An-
tenn marked with long black spots. Legs with indistinct
brown bands and the tips of the femora and tibise and
the terminal joints of the tarsi distinctly black. Thorax
granulated. Prothorax with black markings on the sides
and on the median line; this is interrupted on the front of the
hinder lobe, where there is a curved black line on each side,
before the black median line is continued. Mesothorax with
the hinder two thirds suddenly raised, the raised part with a
black spot and a curved black line on each side in front.
Tegmina with a cone-shaped elevation in front and distinctly
spotted with black, especially on the paler basal half. Costal
area of wings testaceous brown, spotted with black on
the hinder part, and more sparingly elsewhere ; the mem-
branous part of the wings greyish brown, scarcely hyaline.
Hind femora reticulated with black beneath ; ‘first joint
of the middle and hind femora about as long as the two
following; front tarsi missing. Abdomen irregularly and
indistinctly reticulated with black above.
Dimensions.
mm,
Rone "corporis) 32 ete uke ee 64
Tie REEDULIGN 1 RAPP Nee Fog x 6
Te ME SOMON 1. Setopas meter. ! wo oketinmrs, ¢ 5
Ay MLE 101000) oe eee Pee RE 10
» Mmetanoti, cum segm. med. 12
y seements median <2 Js. 2.1.02" G
pect gan bab patie... eS fay, JE 11
9H A UC LT Sc Sore ofoye ara a aovetichare yc Rue Lee 7
| EST TACT Sad iy alt ot eo 100
flab. Penang (lower).
Seems to be most nearly allied to C. maculicoll’s, West-
wood, but with the mesothorax simply raised behind instead
of humped. In markings it greatly resembles Aschipasma
annulipes, Westwood, though much iess heavily spotted; but
its generic characters separate it at once from that species.
436 Mr. W. IF. Kirby—WNotes on Phasmidze
Genus TRIGONOPHASMA, nov.
Size rather large; head smooth, rounded and convex
behind the eyes ; tegmina raised and flattened laterally, thus
forming a triangular hollow cone; wings much longer than
broad ; front femora curved at the base ; mesonotum rarely
more than three times as long as the pronotum.
Allied to Mormessoides, Brunner.
Type, Necroscia rubescens, Sauss.
Genus ORTHONECROSCIA, Kirb., n. n.
|| Necroscta, Brunner, Ann. Mus. Genova, xxxili. p. 84 (1893), nec. Serv.
None of the species described by Serville under Necroscia
appear to belong to the genus as restricted by Brunner to
species with the front femora not curved at the base. Neither
Stal nor Brunner happen to assign any type to Necroscia,
and I therefore rename Brunner’s genus, specifying N. filum,
Westw., as the type of Orthoneuria, and one of Serville’s
? JI ?
most conspicuous species, N. roseipennis, as the type of
Necroscia.
Orthonecroscia pulcherrima, sp. n.
Long. corp. 90, exp. al. 116 mm.
Female.—Wead green, somewhat convex above, with a
medial suleation, on each side of which are three others, con-
verging behind. A square black spot between the antenne
and a large oval spot behind on each side. Antenne very
long and slender, green at the base and afterwards black, with
several white bands. Pronotum with crossing sulci before
the middle; before this green, behind black. Mesonotum
yellowish and slightly granulated above and green below.
Abdomen greenish (colour changed ?), seventh and eighth
segments yellow, with a black spot at the extremity; ninth,
tenth, and anal appendages almost entirely black ; operculum
green, as long as the abdomen. Legs green, banded with
dark brown or blackish. Tegmina strongly carinated and
thickly spotted with golden yellow or, near the margin, with
green. Costal area subhyaline, thickly covered with partly
connected golden-yellow spots, between which are four longi-
tudinal series of blackish spots ; costa bright green. The
membranous part of the wing brownish hyaline, and very
strongly iridescent.
Hab. Borneo.
Closely allied to O. flum, Westw., but much larger and
more variegated in colour.
in the British Museum. 437
Orthonecroscia ruficeps, sp. N.
Long. corp. 88-50, exp. al. 53-65 mm.
Black ; head, base of antenne, and incisions and three
terminal segments of the abdomen sealing-wax red; in the
female the legs are also varied with red. Tegmina black,
paler towards the extremity in the female. Wings with the
costal space black or dark brown, intersected by a fusco-
hyaline line extending from the base to the tip; membranous
part fusco-hyaline, with brown nervures.
Hab. Solomon Islands (Guadalcanar).
A very distinct species.
Genus NrecrosciA, Serv.
Necroscia, Serv. Ins, Orth. p. 250 (1839). (Type roseipennis, Serv.)
Sipylordea, Brunner, Ann. Mus. Genova, xxxili. pp. 84,86 (1892). (Type
stpylus, Westw.)
Necroscia tonguinensis, sp. n.
3 .—Long. corp. 72, long. capitis et pronoti 15, exp. al. 88,
lat. al. 23 mm.
? .—Long. corp. 105, long. capitis et pronoti 22, exp. al.
115, lat. al. 30 mm.
Male.—Pale brown; head rather long, oval, and raised
behind, yellow; median line of head and pronotum suleated ;
head with a row of small granules between the eyes, and
meeting behind them in a V, and several other symmetrical
rows of small granules adjoining and on each side of the
median sulcus ; below these is a brown line below the eye,
continued as a black carina on the sides of the prothorax
and mesothorax, and forming a raised black ridge on the
tegmina, which are otherwise yellowish and obtusely rounded
at the extremity. Antenne pubescent, brown, blackish
towards the base and at the joints; pro- and mesothorax
thickly granulated, the former suleated and the latter slightly
earinated ; abdomen with a black median line, slightly raised,
on several of the segments. Legs pubescent, yellowish
brown, indistinctly mottled with pale brown ; femora blackish
towards the extremity. Costal area of wings yellowish
brown, more yellowish along the costa, and with three or
four long yellow spots, partly surrounded with black, on the
hinder edge ; the membranous part iridescent hyaline, with
yellowish nervures ; those at the base red.
Female.—Brown ; antenne varied with black and pale;
head yellowish, the mouth-parts black in the middle and on
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 30
438 Mr. W. IF. Kirby—Wotes on Phasmidee
the sides ; head and pronotum with slender black central and
lateral lines; thorax granulated; tegmina with a raised
central carina, marked with yellow at the base before the
carina and towards the extremity behind it; costal area of
wings pale brown, the nervures interrupted with blackish ;
rest of wings brownish hyaline, with yellowish nervures,
scarcely interrupted with darker, those towards the base
distinctly red. Wings in both sexes considerably broader
than the length of the head and thorax together.
Hab. ‘Tonkin (Tan Moi), June and July (Fruhstorfer).
Described from three (one male and two female) specimens.
The male is very distinct, but the female is very similar to
NV. sipylus, Westw., except for the breadth and red basal
nervures of the wings. I should not be surprised to find that
the wings of N. tonquinensis were more or less flushed with
red, at least at the base, in perfectly fresl: specimens. It is
one of the largest species of the Necrosciine.
Subfam. IX. AcropuyrzrrinZ.
Genus ACANTHOMIMA, nov.
Allied to Acanthodyta, Sharp; head very long; antennze
with the basal joint very large and flattened, second annular ;
flagellum very short, scarcely longer than the head; meso-
notum granulated, with from 2 to 4 small asymmetrical
spines ; median segment about two fifths as long as the
metanotum ; front femora curved at base and with from 4 to 6
strong serrations between the curve before the middle.
Tegmina and wings rudimentary.
Type, Anophelepis rhipheus, Westw., from Swan River.
Genus ARRHIDA&US, Stal.
Arrhideus phlyctenoides.
M, sea phluctainoides, Rehn, Proc. Acad. Nat. Sci. Philad. 1904,
p. 73.
Long. corp. 48, long. mesonoti 10, lat. 4, long. fem. ant. 13,
exp. al. 388 mm.
Female.—Bright green ; head large, slightly convex, twice
as long as the very small pronotum ; antennee reddish brown,
with more than 30 joints; a yellow line running from the
eye to the back of the head and along the borders of the pro-
and mesonotum. Pronotum with crossing sulcations, the
transverse one well before the middle. Mesonotum mode-
rately broad, finely granulated, and with a slight median
carina. Legs unarmed; femora moderately stout, nearly as
a
in the British Museum. 439
long as the tibix and tarsi together, front femora much waved
at the base. Tegmina almost quadrate, but with the angles
rounded off; a black raised line towards the costa, before
which the colour is yellowish. Wings rather short, costal
area green, membranous area rose-coloured. Abdomen with
the basal segments hardly so long as broad, but the four basal
segments suddenly narrowed and laterally compressed.
Hab. Japan.
Described from four specimens, scarcely varying at all.
Genus Puasa, Licht.
Phasma, Lichtenstein, Cat. Mus. Zool. Hamburg, iii. p, 77 (1796);
Trans. Linn. Soc. Lond. vi. p. 9 (1802); Llliger, Kiif, Preuss. p. 499
(1798) ; Fabr. Suppl. Ent. Syst. p. 186 (1798).
Lichtenstein and Fabricius enumerate many species under
this name, but fix no types. LIlliger, however, mentions
gigas, Linn., and calamus and rossia, Fabr., as the types.
Latreille afterwards specified the type as rossta; but none of
the three species mentioned by Llliger can be taken as the
type, for though all three species were mentioned by Lichten-
stein, he applies the name Mantis to them, not Phasma.
However, the first species mentioned by Lichtenstein under
the name of Phasmais a very close ally of gigas, L., figured by
Stoll as gigas (‘ Spectres,’ pl. i. fig. 1) and described briefly
by Lichtenstein under the name of Phasma empusa. Conse-
quently Illiger’s mention of P. gigas (apart from this being
the first species mentioned under Phasma both by Illiger and
Fabricius) fixes the closely allied P. empusa (Lichtenstein’s
first species) as the type.
Genus HuRYCNEMA, Serv.
EHurycnema magnifica, sp. n.
Long. corp. 200, exp. al. 215, long. tegm. 46, lat. tegm.
20 mm.
Female.—Yellowish green above, more or less varied with
whitish (colours probably changed) ; mesonotum rather long,
slender, and nearly smooth, transversely banded with black
beneath ; tegmina yellowish green, veined below with red;
membrane sea-green. Wings sea-green, the opaque costal
area yellowish green, almost entirely red beneath, except on
the borders, the colour slightly showing through on the upper-
side. Legs strongly carinated, serrated, and spined, as usual
in the genus.
fab. (probably) New Guinea (Crowley Collection).
30*
440 Mr. W. I’. Kitby—WNotes on Phasmidze
This splendid species is one of the largest of the winged
Phasmide. It is allied to EL. versirubra, Serv. (herculeana,
Charp.), from Java, but is abundantly distinct by the longer,
moreslender,and smooth mesonotum, the much longer tegmina,
not marked with white above, and the longer wings, with the
costal area not distinctly red at the base above, but almost
entirely. red below.
Eurycnema viridissima, sp. n.
Long. corp. 186-195, exp. al. 170-175, long. tegm. 38-42,
Jat. tegm. 20 mm.
Female.—Green ; head and pronotum mostly whitish, with
three green bands on the former and two on the latter ; abdo-
men with white incisions and a slender white line on each
side; pronotum paler on the sides than in the middle, smooth,
or with a few small nodules. Meso- and metapectus with a
double row of dark green nodules placed on transverse spots of
the same colour; metapleura with a row of spines. ‘Tegmina
bright green, streaked and spotted with white; the white
spaces are veined with red beneath. Wings sea-green, costal
area tinged with red at the base, and sending out a broad
longitudinal white streak nearly to the margin ; under surface
with the red colouring occupying a corresponding space to
this white streak and with most of the veins red on the basal
third of the wing and along the course of the pale stripe.
Legs green, somewhat irregularly banded and spotted with
whitish. Eggs smooth, oval, black, and shining.
Hab. Moreton Bay and North Australia.
Differs from the North-Australian 2. versifasctata, Serv., ©
in the much longer wings and tegmina, and in the colour of
the latter, which have only one broad longitudinal streak in
E. versifasciata.
‘The Museum possesses specimens of Hurycnema from
Timor and Timor-Laut, but not in sufficiently good condition
to be determined. ‘The only described species not represented
in the Museum is /, Beauvoist, Serv., from Java, in which
the pronotum is stout and granulated, and the tegmina and
the costal area of the wings are uniform bright green.
Subfam. X. HurycanrHin Zz.
The genera Karabidion, Eurycantha, and Canachus are
placed by Brunner at the end of his Clitumnide, but they
have so little resemblance to the other genera of that family,
and so much (except in the tibiee being carinated to the tips)
to the Heteropterygine, that I think it better to remove them
to the neighbourhood of the latter insects.
in the British Museum. 441
Genus HUBULIDES, Stal.
Hubulides spuria, sp. n.
Lurycantha spuria, Westw., MS.
Long. corp. 55, long. pronoti 10, lat. 8 mm.
Male.— Pale yellowish grey, varied with reddish brown on
the head above, and more or less on the sides of the body.
Antenne thick, 17-jointed, the scape and second joint paler
than the rest; joints 2 and 4-6 transverse, the rest longer
than broad; joints 7-11 increasing gradually in length;
joint 12 as short as joint 7, the rest again gradually in-
creasing in length, the terminal joint being the longest and
slenderest. Head convex above and depressed in front; a
slender yellow median line, and behind and within the level
of each eye two narrow sulcations, converging behind but not
meeting. Median line with a deep sulcus which extends to
the extremity of the abdomen, but is interrupted on segments
4-6 of the latter. Pronotum with the transverse sulcus
placed before the middle; the upper surface is widened behind,
and on each side of the median line is a brown band, curving
outwards, on which stand three tubercles, behind the last of
which are a few smaller ones, irregularly placed; upper
lateral carina convex. Mesonotum rather broader in front
than behind, thickly tuberculate for two thirds of its length,
and slightly denticulate on the lower lateral carina. Abdo-
minal segments transverse, considerably broader than long,
and truncated behind; all except the three terminal ones,
which are narrower than the others, laterally sublobate.
Cerci pale, very thick, hardly pointed at the tips, about half
as long as the last segment, beyond which they project.
Legs very short and stout, front and hind femora and tibia
all about as long as the mesonotum, middle ones rather
shorter; they are slightly carinated and unarmed; hind
femora with several small teeth beneath on the inner carina,
and two large subterminal ones on the outer, preceded by
some obsolete ones ; the median line beneath is also tubercu-
late. Last joint of tarsi very large, as long as all the rest
put together, which are very short, except the first joint of
the front tarsi, which is concave above and as long as joints
2-4 together; claws and arolia also very large.
Hab. Australia.
Appears to belong to Stal’s genus Hubulides, founded on
E. alutaceus, Stal, from the Philippines, a species I have not
seen. In this, however, all the femora are dentated beneath.
AL? Mr. W. F. Kirby—Wotes on Phasmide
Genus EurycanTHa, Boisd.
Eurycantha Willeyt, sp. n.
Ewrycantha horrida, Sharp, Willey, Zool. Results, p. 85, pl. vii.
figs, 7-9, pl. ix. figs. 46, 46 a, b (egg) (1898), nec Boisd.
Long. corp. 120-130, lat. pron. 17-20 mm.
Male.—Black ; head with two moderate-sized spines wide
apart, nearly halfway between the eyes and the occiput, and
two smaller ones, nearer together, rather further back; pro-
notum with 2 large lateral spines in front and 1 behind;
mesonotum with 7 or 8 strong lateral spines, the last some
distance behind the penultimate one and near the hinder
edge; there are also less regular rows of smaller spines below
them and on the mesopleura; metanotum and metapleura
with large irregular Jateral spines, the largest being two about
the middle, and another above the hind coxa; segments of
the abdomen (except the last) each with 3 strong lateral spines,
and with one or two terminal large tubercles at a higher level;
segments 7-9 with a short terminal tooth on the median
line ; upper surface of the body except at the sides spinulose,
but with scattered granules; coxe spined; 4 first femora
thickened and with regular but rather widely separated teeth
on the carine; 4 first tibie with 4 or 5 moderately large
teeth on each side beneath ; hind femora greatly dilated, and
with 3 large teeth beneath, the last very large and curved
backwards; there are also strong terminal spines on the
carine beneath; hind tibiz with 3 large teeth beneath, the
middle one double, besides smaller ones towards the base and
on each side at the extremity.
Female more ferruginous ; the spines smaller, but similarly
arranged ; the hind femora are much less thickened, and the
third spine is not much larger than the others.
Hab. New Britain.
Nearest to #. calearata, Luc., but much less strongly
spined. The true 4. horrida, Boisd., differs from most of the
allied forms by the lateral spines on the abdominal segments
being smaller and more numerous.
Eurycantha portentosa, sp. n.
Long. corp. 170, lat. mesonoti 22-26 mm.
Female.—Black ; antenne, legs, and under surface inclining
to ferruginous ; spines arranged nearly as in the last species ;
much more strongly granulated on the upper surface, and
with a transverse row of short spines before the extremity of
most of the abdominal segments. There are sometimes
in the British Museum. 443
additional small spines between the three larger ones on the
sides of each abdominal segment.
Hab. Rossel Island, Louisiade Archipelago.
The largest and broadest species known.
Eurycantha sifia, sp. n.
Long. corp. 104-129, lat. mesonoti 18-20 mm.
Male.—Mahogany-brown, rather shining; head with two
large spines behind and rather within the level of the eyes,
and two smaller ones behind these, nearer together ; sometimes
a pair of tubercles nearer the front; pronotum with 2 large
lateral spines in front and 1 behind; mesonotum with 2
small central spines on the front edge and about 8 moderate-
sized spines on the upper lateral margin, but only 2 or 3
small ones on the mesopleura towards the hinder end; lateral
spines of metanotum nearly as in H. Wlley?, but more
numerous; abdomen with 3 lateral spines on each segment,
the first placed rather higher than the others, which stand on
a carina on which other rudimentary spines are often placed ;
upper surface of thorax and abdomen with scattered tubercles ;
a transverse row of small terminal spines on most of the
abdominal segments, best developed on the hinder ones; a
distinct median carina on the three segments before the last,
rising into a strong spine at the extremity. Legs armed
nearly as in Z. Willeyi; the large spine less curved,
Female darker brown, but otherwise very like the male ;
mesopleura with more numerous small spines below the larger
ones; spines of the metanotum smaller than in the male;
abdomen with the hinder half carinated to the extremity ;
hind femora beneath with 4 or 5 spines (before the terminal
ones) of nearly equal length.
Hab. Thursday Island.
Appears to be a common species. Belongs to the group of
E. calcarata, Luc. Differs from Z. calcarata in the smaller
and less numerous spines, and from HL. Willeyt (inter alia) by
the conspicuous pair of spines in front of the mesonotum.
Subfam. XI. HereropreryGin2z.
Genus HeTEROPTERYX, Gray.
The type of this genus is Phasma dilatata, Parkinson, the
male of which is, I believe, Phasma (Hurycantha) graciosa,
Westw. (not at present represented in the Museum), on which
Stal founded his genus Leocrates.
444 Mr. W. F. Kirby—Notes on Phasmidee
Genus HAANIELLA, Kirb., n. n.
\| ZZeteropterya, Haan; Stal (nec Gray).
Phasma (Leteropteryx) Miilleri, Haan, may be regarded as
the type.
Subfam. XII. Awzsomorpuivs.
I have no additions to make to this subfamily.
Subfam. XIII. Perrsoprvz.
These peculiar insects differ much from all the others
placed by Brunner in his heterogeneous family Phasmidie,
and in some cases the clefts at the end of the tibiz beneath
are very slightly marked.
Genus ACANTHOCLONIA, Stal.
Acanthoclonia (?) paradowa, sp. n.
Female.—Dark brown; antenne, palpi, and legs clothed
with a thick felty pubescence. Head with the upper part
much raised, having a trilobate diverging excrescence on each
side and a row of three pairs of raised tubercles between ;
the sides and front of the head are also set with conspicuous
tubercles less regularly arranged. ‘The anterior lobes are
much larger than the others, and converge in front. Of the
antennz, which incline to reddish towards the end, twenty
joints remain ; they are cylindrical ; the third is the longest,
but the remainder increase very gradually in length after the
fourth ; the scape is broad and flattened, with a raised carina
on each side above, and a Jarge lobe below ; the second joint
is thickened, forming a broad cone. Legs short and stout ;
femora more or less laminate-dentate on the upper carine,
the foliations slightly converging above; the tibize the same,
with several elevations on the front tibize and one or two on
the others; the outer lower carina of the middle femora is
armed with three large teeth. ‘Tibize beneath with large
terminal triangular clefts. ‘Tarsi with the fifth joint long,
the first shorter, and the middle ones very short, decreasing
in length. '‘Tegmina rounded, rather longer than broad,
extending just beyond the base of the median segment ; wings
not visible, Lower appendages of the abdomen yellowish.
tn the British Museum. 445
Dimensions.
mm.
Tone." Corporis’ i. cis vd.« tele postin ete Ce
Fo GUPEGIB SS SALTS, Sana are. ote vise oe fi
Saab OMGDILES Jatin) a oh che) sfo:st dats ieratt oe Bes a 8
Poa MRE ONO LI apate spas ors! wersrate BO Gn oe Jy 10
RAUL SS29 22715 171 1 a ee af it
erg ACM AMD ay cha cee a Sree rac Uh
Lab. Santarem, Lower Amazons, March 1896. Taken in
the forest by Mr. F. O. Pickard-Cambridge.
The lower carine of the thorax and the cox: are dis-
tinctly tuberculate. The thorax is strongly granulated and
tuberculate ; the prothorax has rows of small tubercles in
front, behind, and at the sides; also in the middle, where
two are larger and more conspicuous than the others. he
mesothorax has three broad obtuse spines on each side of the
double median carina, two in front, and the other about the
middle. Abdomen with irregular zigzag lines of rugosities,
those on the back of the penultimate segment and the one
before enclosing long oval spaces.
A very peculiar species, probably belonging to a new
genus, which, however, I do not wish to found upon a single
specimen, perhaps immature. It is not unlikely to possess
wings when fully developed, but it differs conspicuously from
Prisopus and its allies by the much broader and shorter
tegmina,
Subfam. XIV. PsrvpornHasurv2z.
Phasmide, pt., Brunner,
Genus Dagaca, Brunner.
Brunner proposed this genus for an undescribed Bornean
species of which the Museum possesses a specimen, unfortu-
nately in too poor condition to describe.
Genus OLCYPHIDES, Griff.
|| Phocylides, Stal (nec Pascoe).
Olcyphides tridescens, sp. n.
Long. corp. 73, long. tegm, 6, lat. 3, exp. al. 93, lat.
24 mm.
Lremale.—Head black below and at the sides as far as the
level of the eyes; a black space between the antenneand a black
curve behind the ocelli; antennz black, the scape greenish, the
446 Mr. W. F. Kirby—Notes on Phasmide
joints with narrow pale rings towards the base and at least
four broad whitish or green belts beyond; head and pronotum
sulcated on the median line; pronotum longer than broad,
green above and black below and on the sides, transverse
sulcus placed before the middle, behind it on each side is a
broad black dash. Mesonotum brownish green above, with a
median bright green line; sides and under surface black, the
former with two longitudinal yellowish lines. “Interalary space
greenish ; abdomen mahogany-brown, seventh segment
reddish, the last three segments varied with green and
brown. Abdomen brown beneath, except the operculum,
which is green; cerci brown, rather short and thick; legs
purplish brown, broadly belted with green. Tegmina green,
with the usual hump; extremity truncated, oblique, costa
shorter than inner margin. Wings with the costal area of a
subhyaline rosy grey, the longitudinal nervures bright green ;
a purplish-brown costal stripe, narrowly bordered towards
the base by yellow on the extreme costal edge, traverses the
greater part of the wing, Membranous part of the wing
brownish subhyaline, with a very strong coppery iridescence ;
the nervures green towards the base, and most of the trans-
verse nervules greenish white.
Hab. Trinidad.
Genus I@nacta, Rehn.
Pseudophasma, Bol.
Ignacia appendiculata, sp. n.
Light brown; antenne with the two basal joints and more
or less of several of the succeeding ones reddish brown, the
terminal half of the fourth blackish; head twice as long as
broad, with a black band extending backwards from the
antenne, but well within the eyes, over the pro- and meso-
notum; pronotum shorter than the head, the sides and the
sulcations pale; mesonotum rather longer than the head and
pronotum together, and with six long slender filaments rather
than spines on the upper surface, black, tipped with pale in
the male, and wholly pale in the female; the first pair on
the front margin nearly obsolete in the male, the second
rather further, and the third about the middle; tegmina
brown, with a large, pointed, conical elevation directed
towards the base; behind this the colour is yellowish ;
wings with the costal area light brown; a whitish streak
towards the base of the costa, membranous portion greyish
subhyaline ; legs long and slender, all the femora clavate
towards the extremity, and the front femora much waved.
in the British Museum. 447
Dimensions.
Siete
mm. mm,
One COUP hea ete ee eae ts 53 7
ie LCOirarern tee ce eres Lito 6 10
Eales PRAM eek 8G. IS 64 102
Dioneeitenn, antes se sisitents wt ace 18 22
Flab. Nauta (Degand).
Described from one male and one female, both in rather
poor condition.
Genus PSEUDOPHASMA, Kirb.
Pseudophasma inca, sp. n.
Male.—Black ; head scarcely broader than long, pronotum
half as long again as broad, granulated, speckled with yel-
lowish, and with the lateral carina narrowly yellowish ;
a deep oblique depression before each of the front angles ;
mesonotum granulated with yellowish, metanotum and
base of abdomen rufous above; tegmina broadly oval, the
costa greatly arched, reticulated with yellow, the inter-
mediate space brown, and a large, black, obliquely oval spot
before the extremity. Costal area of wings dark brown,
yellowish, and with yellowish transverse nervures towards
the base ; membranous area smoky hyaline.
Lemale.—Upper surface of head, pro- and mesonotum
brown, bounded by the black colour of the sides; tegmina
with the black blotch much larger, curving round to the base ;
area behind uniform light brown. Costal area of wings
light brown, mottled with darker; base pale; metanotum
with borders and sutures varied with yellow, and basal
segments of abdomen indistinctly marked with yellow.
Antenne black, banded in the female only with ferruginous
towards the extremity.
Dimensions.
Petar
mm. mm
IONE. COUP. «) 20-<.n1 a clare cuternnarae 47 is
bye | IMOBONOU © tee cies tigaereees 5 6
Bieps Ol!” Ss ste arate lcthersterer tare ere 70° 122
Hab. Paleazu, Peru.
A fine species, belonging to the same group as P. phthisicum,
Linn. ; but in that species the tegmina are much raised, and
the femora are reddish at the base.
448 Notes on Phasmidee in the British Museum.
Pseudophasma Cambridge, sp. n.
Female-—Head broader than long, testaceous, with a
narrow brown carina above, expanding and ceasing in a
small triangular spot between the antenne; the sides of the
head nearly to the level of the upper part of the eyes are
black ; face testaceous, a transverse reddish mark in front
below the level of the antennz; palpi reddish brown, the
inner side and terminal joint more yellow. The antenne are
finely ciliated (18 joints remain), testaceous yellow to the
eleventh joint and then black, with pale rings towards the
base of the twelfth segment, and on the extremity and base
of the fourteenth and fifteenth and sixteenth and seventeenth
respectively, and at the tip of the eighteenth. The scape,
second joint, and base of the third are thickened ; the third is
nearly as long as the fourth and fifth together, the fifth being the
shortest, the rest gradually lengthening, though the eighteenth
is a little shorter than the preceding; all the joints beyond
the second are long and cylindrical. Prothorax and meso-
thorax testaceous above, with a median groove; the thorax,
below the lateral carine, and the abdomen are black. ‘The
hinder two-fifths of the mesothorax is raised; the front part is
bordered on the lateral carinee with a row of short sharp
spines, the flat space between being sparingly and irregularly
granulated. The tegule are humped, strongly reticulated,
and testaceous yellow inside to the summit of the hump, and
black outside. ‘The wings are dark reddish brown on the
costal area and greyish brown on the membranous area.
The legs are testaceous, the femora black, testaceous at the
tips beneath on the first four femora, and wholly so beneath
on the hind femora. ‘lhe trochanters and coxe are wholly
blackish. The terminal segments of the abdomen are
carinated above and provided with a deep pouch below; the
cerci are short, thick, and obtuse. The legs are long and
slender, the middle legs shortest.
Dimensions.
mm,
TON ACOMpOris 7G sk). hicsate s saree eee eee 58
gg CBDULIS' A) Eee Se ns eae ae 4
9 iy LOUGINT- venelerciaelcis oedensvetetemerst ees ot
$< MRESOMOL En LEON oc sere eee 8
Bxpial: 6.5 es laeise tases oe eee S 57
Long. femeant. 4 isis leis tein sateen eke 20
Lab. Forest, Santarem, Lower Amazons, March 1896.
On new Species of Barbus from Lake Victoria. 449
Closely allied to Phasma putidum, Bates (also from San-
tarem), but differing in the colour of the antennz, the prickles
on the thorax, &e.
A single specimen only, taken by Mr. F. O. Pickard-
Cambridge.
Subfam. XV. AscurpasMInz.
Subfam. XVI. Puyrzrimz.
I have no additions to make to these subfamilies. The
genus Aschipasma, Westw., is often misspelt Aschiphasma.
LII.—Dvraynoses of Three new Species of Barbus from
Lake Victoria, By G. A. BouLENGER, F.R.S.
Barbus nummifer.
Weis: Aalto. I lat 37-39) Eh te,
3
Depth of body 33 to 4 times in total length, length of head
41 to 44 times. Snout rounded, as long as eye, which is 33
to 4 times in length of head; interorbital width 24 to 23 times
in length of head ; lips feebly developed, interrupted on tlie
chin; barbels 2 on each side, anterior as long as eye or a
little shorter, posterior 1} to 14 diameters of eye. Last simple
ray of dorsal very strong, bony, not serrated, as long as head.
Ventrals below origin of dorsal. Caudal peduncle 13 to
twice as long as deep. 4 scales between lateral line and root
of ventral. A series of 3 to 6 round blackish spots on each
side,
Total length 130 mm.
Several specimens.
Barbus macropristis.
Dory 7 A. TUS 4? Bi tat 392 Se tre =,
ee
og
Depth of body equal to length of head, 4 times in total
length. Snout rounded, 8} to 4 times in length of head ;
diameter of eye 4 to 44 times in length of head, interorbital
width 22 times; lips feebly developed; barbels 2 on each
side, anterior 4 diameter of eye, posterior as long as eye.
Last simple ray of dorsal very strong, bony, strongly serrated
behind, nearly as long as or a little longer than head. Ven-
trals entirely in advance of dorsal. Caudal peduncle twice as
450 Mr. G. A. Boulenger on Three new Snakes,
long as deep. 3 scales between lateral line and root of
ventral. No markings.
Total length 128 mm.
Two specimens.
Barbus Doggettt.
L
D. TH 8,5 (AES. Mb Aate 298 Alisa.
Depth of body equal to length of head, 32 times in total
length. Snout rounded, 33 times in length of head ; diameter
of eye 32 times in length of head, interorbital width 3 times ;
lips feebly developed ; barbels 2 on each side, minute. Last
simple ray of dorsal not ossified, as long as head. Ventrals
below anterior rays of dorsal. Caudal peduncle nearly twice
as long as deep. 2 scales between lateral line and root of
ventral. No markings.
Total length 96 millim.
A single specimen.
These fishes were obtained by the late Mr. W. G. Doggett,
and have been presented to the British Museum by Col.
Delmé Radcliffe.
LIII.—Descriptions of Three new Snakes.
By G. A. BouLenGer, F.R.S.
Hydrethiops levis.
Rostral broader than deep, just visible from above and in
contact with the internasal, which is divided or semidivided
along the middle line ; frontal once and one third as long as
broad, as long as its distance from the end of the snout,
shorter than the parietals ; loreal usually fused with the pra-
frontal; one pree- and two postoculars ; temporals 1+2;
nine upper labials, fourth and fifth entering the eye, sixth
and seventh in contact with the parietal ; two pairs of chin-
shields, the anterior in contact with four or five lower labials.
Scales perfectly smooth, in 21 rows. Ventrals 154-163 ;
anal divided; subcaudals 51-52. Yellowish or reddish
brown above, with a series of large, dark olive-brown, black-
edged spots, which may be confluent posteriorly into a zigzag
band ; head uniform olive-brown above and on the sides ;
Mr. G. A. Boulenger on Three new Snakes. 451
lower parts black, uniform or with a median series of small
whitish spots on the anterior part of the body.
Total length 570 mm. ; tail 110.
Two specimens from Efulen, S. Cameroon; collected by
Mr. G. L. Bates.
Atractus vertebralis.
Snout rounded. Rostral small, broader than deep, just
visible from above ; internasals very small ; preefrontals as
long as broad; frontal as long as broad, as long as the pre-
frontals, two thirds the length of the parietals ; loreal twice
and a half as long as deep; two postoculars ; temporals 1+ 2;
seven or eight upper labials, third and fourth or fourth and
fifth entering the eye; four lower labials in contact with the
single pair of chin-shields, which are rather elongate, mode-
rately broad, and separated from the symphysial. Scales in
17 rows. Ventrals 173; analentire; subcaudals 21. Brown
above, with small black spots and a black vertebral streak
edged with yellowish ; upper surface of head blackish ; upper
lip yellowish ; ventral shields yellow in the middle, black on
the sides, one or two shields here and there entirely black
and forming cross-bars on the belly.
Total length 470 mm.; tail 35.
A single female specimen from Santo Domingo, Carabaya,
Peruvian Andes, altitude 6000 feet; collected by Mr. G.
Ockenden.
A pistocalamus Pratti.
Snout short, rounded. Rostral a little broader than deep,
the portion visible from above measuring one third its
distance from the frontal; internasals half the length of the
preefrontals ; frontal slightly longer than broad, as long as
its distance from the end of the snout, much shorter than the
parietals ; nostril between two nasals*, the posterior forming
a suture with the single preeocular, which is nearly twice as
long as deep; a single postocular; temporals 1-+1; six
upper labials, third and fourth entering the eye; three lower
labials in contact with the anterior chin-shields; posterior
chin-shields smaller, separated by a large scale. Scales in
15 rows. Ventrals 190; anal divided; subcaudals 41, partly
single, partly paired. Olive-brown above; an oblique
yellowish streak on each side of the nape; upper lip
* The discovery of this species necessitates an alteration in the generic
diagnosis (Ann. Mus. Genova, 2, xviii. 1898, p. 705), as the first labial
and the internasal do not border the nostril.
452 On new Species and Varieties of Cataulus.
yellowish ; lower parts yellowish, with a median series of
olive-brown spots which, after the anterior fourth of the body,
become confluent into a band.
Total length 855 mm. ; tail 50.
A single male specimen from Dinawa, Owen Stanley
Range, Brit. New Guinea, altitude about 4000 feet ; collected
by Mr. A. E. Pratt.
LIV.—Deseriptions of some new Species and Varieties of
Cataulus from the Collection of the late Hugh Nevill, Esq.
By Hucu Futron.
Cataulus rugosa, sp. n.
Shell very narrowly umbilicate, subfusiform, moderately
solid, colour light yellowish brown, nucleus smooth, sculptured
below with somewhat nodulous oblique striz, which give a
malleated appearance to the shell; whorls 64, moderately
convex ; basal carina moderately produced ; aperture circular,
reddish brown within ; peristome yellowish, continuous ; basal
canal semicircular, situate at centre of basal portion of the
peristome.
Maj. diam. 5; alt. 11} mm.
Loc. Ceylon.
This form is nearest to C. marginatus, but is much smaller,
not so slender, and the suture is not margined.
Cataulus Sykesi, sp. n.
Shell narrowly umbilicate, subfusiform, solid, uniform light
yellowish to uniform reddish-brown colour, arcuately striated,
the striae rather blunt and not very conspicuous; whorls
nearly 7, slightly convex; basal carina prominent, with a
conspicuous inner ridge ; aperture subcircular, reddish brown
within ; peristome whitish, very much thickened but scarcely
duplex, continuous ; aperture of basal canal subcircular,
situate slightly to the left of the centre of base of peristome.
Maj. diam. (yellow form) 63 ; alt. 145 mm.
- » (reddish-brown form) 63; alt. 14 mm.
Loc. Ceylon.
his form bears a general resemblance to C. duplicatus, Pf.,
but is smaller, has less whorls, and the suture of the earlier
whorls is not margined as in that species.
On Mollusca from the Bay of Bengal &e. 453
The penultimate whorl of duplicatus is wider in proportion
to the last whorl than in Sykes? ; the latter is also distinguished
by its prominent inner basal ridge at the umbilical area.
Cataulus marginatus, Pf., var. crenulata, nov.
Slightly broader than typical marginatus, less strongly
malleated, and lacking the distinctly margined suture of that
species; of a light reddish colour, and crenulated at and below
the suture of the middle whorls, the antepenultimate showing
it more distinctly.
Maj. diam. 6; alt. 15 mm.
Loe. Ceylon.
Cataulus Nevilli, Sykes, var. jflaveolabris, nov.
Lighter-coloured and with a yellow peristome, the latter
being more on a plane with the spire than in typical Nevill:,
which is generally somewhat produced forward at the basal
portion.
Maj. diam. 115 alt. 25 mm.
Loe. Ceylon.
LV.—Natural History Notes from H.M. Indian Marine
Survey Steamer ‘ Investigator, Commander T. H. Heming,
R.N.—Series III., No. 1. On Mollusca from the Bay of
Bengal and the Arabian Sea. By Evear A. Smiru, 1.8.0.
[Continued from vol, iv. p. 251. ]
In these ‘ Annals’ for 1899, vol. iv. pp. 237-251, diagnoses
were given of thirty-five new species from the collection
about to be described. The publication of such lists as the
following are of importance as regards our knowledge of
both geographical and bathymetrical distribution. Many of
the species were obtained at Stations 229, 232, and 233, the
exact positions of which are as follows :—
Station 229.— Lat. 9° 29’ 34” N., long. 75° 38’ E.:
360 fath.; green mud.
Station. 232. — Lat. 7° 17” 30" N-; long. 76° 54 EL:
430 fath.; grey mud.
Siation, 293.— ‘Lat. 13°17) 357 "N= lone’ 93> 10" * he:
185 fath.; sand.
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 3]
454 Mr. EX. A. Smith on Mollusca from the
The thirty-five species already referred to have been figured
in the “Illustrations of the Zoology of the ‘ Investigator,’ ”
Mollusca, pls. ix.—xui. (1901). The sixteen new species now
described will be figured in a future part of the same work.
Conus planiliratus, Sowerby.
Conus planiliratus, Smith, Ann, & Mag. Nat. Hist. 1894, vol. xiv.
p. 159.
Hab. Coromandel coast, 12 fath.
Conus Sowerbii, Reeve.
Conus sinensis (Sowerby ?), Reeve, Conch. Icon. pl. xv. fig. 77 a.
Conus Sowerbit, Reeve, Conch. Icon., Suppl. Emend. p. 2.
Hab. Off Coromandel coast, in 41 fath.
Conus turriculatus, Sowerby.
pce ea Smith, Ann, & Mag. Nat. Hist. 1894, vol. xiv.
p. 160.
Hab. Off Mangalore, Malabar coast, 26-30 fath.
The largest specimen of this species in the Cuming Collec-
tion, hitherto confused with C. Sowerdii, is 35 mm. in length,
This is rather larger than the type, and, judging from the
thinness of the lip, it is scarcely adult.
Conus semisulcatus, Sowerby.
Conus semisulcatus, Sowerby, Proc. Zool. Soc. 1870, p. 257, pl. xxii.
fig. 18; Thes. Conch. vol. v. p. 258, pl. 508. fig. 666 (bad !).
Hab. ? (Sowerby); off Vizagapatam coast, 20 fath.
The type of this species in the collection of the British
Museum is a young shell only 21 mm. in length. The more
mature, possibly adult, examples from Vizagapatam, 33 mm.
long, agree exactly with it in all other respects. The surface
is clothed with a thin deciduous periostracum, which exhibits
a few distant setose lines or ridges upon the body-whorl and
is coarser and lamellated upon the spire, which has about
five whorls succeeding the smooth glassy protoconch, finely
coronated. The sulci upon the anterior end of the shell are
about eleven in number.
Conus aculeiformis, Reeve.
Conus aculeiformis, Reeve, Conch. Icon. pl. xliv. fig. 2400; Sowerby,
Thes. Conch. vol. iii. pl. xvi. fig. 370.
Hab. Philippine Islands (Reeve) ; Holothuria Bank, N.W.
Bay of Bengal and the Arabian Sea. 455
Australia, 15-30 fath. (Brit. Mus.); off Vizagapatam, 25
fath., off Coromandel coast, 41 fath., off Mangalore, 26-30
fath. (‘ Investigator’).
The series of specimens from the above localities shows
that the species varies somewhat in the strength of the sculp-
ture and the depth of the coloration. The upper whorls of
the spire may or may not be coronated. In the type they
are strongly nodose, whilst in the specimens from N.W.
Australia the coronation is almost obsolete, and in the
examples from the Indian localities it is entirely absent.
The transverse ridges upon the body-whorl are coarser and
most prominent in the typical form and comparatively
flattened in the Australian specimens. There are also other
minor differences in the various examples which it would be
tedious to explain in words, although they are quite appa-
rent and interesting on comparison.
Conus Sieboldii, Reeve.
Conus Steboldi, Conch. Icon., Suppl. pl. i. fig. 269; Sowerby, Thes.
Con. vol. iii. pl. ecii. fig. 869; Weinkauff, Conch,-Cab. ed. 2, p. 285,
pl. xlix. fig. 6.
Hab. Japan (Reeve, Lischke, &c.); Stations 229 and 232,
off Malabar, in 360 fath., and off Travancore coast, in 430
fath. (‘ Investigator ’).
Only one of the five specimens examined shows any traces
of the scattered brownish blotches which are characteristic of
this species. This absence of colour is not remarkable, as
these examples were from deep water, probably much deeper
than that whence any of the previously recorded specimens
were obtained. It will be remembered that the occurrence
of Ranella (Biplex) perca, a well-known Japanese form, has
already been recorded from deep water off Colombo*, and
also the Japanese Xenophora pallidula from 188 fath. off the
Andaman Islands+. It is therefore interesting to find
another form hitherto supposed to be exclusively Japanese
occurring in the Bay of Bengal.
The apex of the spire in these specimens, which were
dredged alive, is eroded, so that the slight ‘ coronation” of
the whorls is destroyed. This would probably be the case in
all specimens obtained at this particular station.
* Smith, Ann. & Mag. Nat. Hist. 1895, vol. xvi. p. 6.
+ Sowerby, Proc. Malac. Soe. vol. i. p. 38.
ob
456 Mr. E. A. Smith on Mollusca from the
Pleurotoma vagata, Smith.
Pleurotoma vagata, Smith, Ann, & Mag. Nat. Hist. 1895, vol. xvi.
p. 3, pl. i. fig. 3.
Hab. Station 233, off Andaman Islands, in 185 fath.; also
Station 229, off the Travancore coast, in 360 fath.
The specimens from the first locality agree in every respect
with the unique type from 200-350 fath. off Trincomalee.
The infrasutural keel is generally somewhat reddish, and the
central carina is spotted with the same colour between the
tubercles, which in some specimens become obsolete upon
the body-whorl. The concavity of the upper part of the
whorls becomes more obvious as the shell increases, so that
it forms a deep channel upon the body-whorl m some speci-
mens. In the shells from off the Travancore coast the keel
at the suture is much more feeble than in the typical form.
Pleurotoma congener, Smith.
Pleurotoma congener, Smith, Ann. & Mag. Nat. Hist. 1894, vol. xiv.
p. 160, pl. iii. figs. 4, 5.
Hab. Station 229, off Travancore coast, in 360 fath.; also
Station 233, off Andaman Islands, in 185 fath.
The specimens obtained off the Travancore coast are
longer and narrower than the typical form, with a narrower
tuberculated band round the middle of the whorls. Five out
of the eight specimens examined, all dead and more or less
broken, have the peculiar swelling on the upper part of the
columella which was mentioned as occurring in some examples
obtained off Colombo. The measurements of the largest
specimen are :—
Length 62 mm., diam. 20; aperture 20 long, 8 wide.
Pleurotoma optata, Smith.
Pleurotoma optata, Smith, Aun. & Mag. Nat. Hist. 1899, vol. iv.
p. 288; lust. Zool. ‘ Investigator,’ pl. ix. figs. 1, 1a.
Hab. Station 232, off South India, 480 fath.; and Station
229, off Travancore in 360 fath.
Pleurotoma fusca, Hombron & Jacquinot, var.
Pleurotoma fusca, H. & J., Voy. Pole Sud, p. 111, pl. xxv. figs. 19, 20.
Hab. Station 240, off Andaman Islands, 194 fath.
Two specimens, paler than the type, almost white, with a
slightly shorter anterior canal. Pl. gemmata, Hinds, may
be the same as this species, but the spire seems to be more
Bay of Bengal and the Arabian Sea. 457
slender. Pl. amabilis, Weinkauff, is very closely allied, if
not identical. Hinds’s locality, “California,” may yet be
confirmed.
Pleurotoma jubata, Hinds.
Pleurotoma jubata, Hinds, Reeve, Conch. Icon. fig. 52.
Hab. Off Mangalore, Malabar coast, 26-30 fath.
One specimen, like the type, but with the beaded keel
scarcely at all beaded.
Pleurotoma acutigemmata, var. minor.
Pleurotoma acutigemmata, Smith, Ann. & Mag. Nat. Hist. 1877,
vol, xix. p. 489.
Hab. Off south coast of Ceylon, 34 fath.
A single specimen, only 13 mm. in length, like the type
in form and colour, but with the gemmate keel almost smooth.
Pleurotoma unedo, Valenciennes.
Pleurotoma unedo, Valenciennes, Kiener, Coq. Viv. p. 19, pl. xiv. fig. 1;
Reeve, Conch. Icon. fig. 12.
Hab, Eight miles south of Puri, 13 fath.
Pleurotoma (Surcula) tornata (Dillwyn).
Surcula tornata, Tryon, Man. Conch. vol. vi. p. 237, pl. v. fig. 62.
Hab. Same as preceding species.
Pleurotoma (Surcula) symbiotes, Wood-Mason & Alcock.
Pleurotoma (Surcula) symbiotes, Smith, Ann. & Mae. Nat. Hist. 1894,
vol. xiv. p. 161, pl. iii. figs. 7, 8.
Hab. Station 233, off Andaman Islands, in 185 fath.
These specimens do not differ from the type, which was
obtained in 1043 fath. off Southern India. Being in fresh
condition they are coated all over with the very thin peri-
ostracum mentioned in the description.
Pleurotoma (Surcula) Thurstoni, Smith.
Pleurotoma (Surcula) Thurstoni, Smith, Ann. & Mag. Nat. Hist. 1896,
vol. xvii. p. 369.
Hab. Off Trincomalee, in 200-350 fath.; and Station 229,
off Travancore coast, in 360 fath.
One specimen from the latter locality is larger than the
type, being 55 mm. in length and 16 in width,
458 Mr. E. A. Smith on Mollusca from the
Pleurotoma (Surcula) breviplicata, Smith.
Pleurotoma (Surcula) breviplicata, Smith, Ann. & Mag. Nat. Hist.
1899, vol. iv. p. 238; Tllust. Zool. ‘ Investigator,’ pl. ix. figs. 3, 3 a.
Hab. Station 233, off Andaman Islands, in 185 fath.
Pleurotoma (Surcula) eurina, Smith.
Pleurotoma (Surcula) eurina, Smith, Ann. & Mag. Nat. Hist. 1899,
vol. iv. p. 239; Lllust. Zool. ‘Investigator,’ pl. ix. figs. 4, 4 a.
Hab. Station 232, off South India, in 430 fath.
Pleurotoma (Surcula) precipua, Smith.
Pleurotoma (Surcula) precipua, Smith, Ann. & Mag. Nat. Hist. 1899,
vol, iv. p. 289; Illust. Zool. ‘ Investigator,’ pl. ix. figs. 5, 5 a.
Hab. Station 229, off Travancore coast, in 360 fath.
Pleurotoma (Surcula) arcana, Smith.
Pleurotoma (Surcula) arcana, Smith, Ann. & Mag. Nat. Hist. 1899,
vol. iv. p. 2389; Illust. Zool. ‘ Investigator,’ pl. ix. figs. 6, 6 a.
Hab. Station 233, off Andaman Islands, in 185 fath.; and
Station 229, off Travancore coast, in 360 fath.
Pleurotoma (Surcula) Margarite, sp. n.
Testa fusiformis, turrita, albida, epidermide tenuissima lutescente
induta; spira elongata, acuminata ; anfractus 12, in medio angu-
lati, nodose oblique plicati (plieis inferne attenuatis), supra con-
cavi, infra subconyexi, undique spiraliter tenuiter et confertim
striati lineisque incrementi flexuosis tenuibus sculpti, ultimus
infra angulum convexus, antice breviter rostratus; apertura
elongata, piriformis ; labrum tenue, valde arcuatim prominens,
superne late et profunde sinuatum; columella in medio recti-
uscula, antice obliqua.
Longit. 60 mm., diam. 20; apertura cum canali 27 longa, 8 lata.
Hab. Off Andaman Islands, 405 fath.
In the body-whorl there is a slight convexity or rounded
ridge just below the suture and above the excavation, below
which occur the oblique nodose plications which gradually
diminish in strength as the aperture is approached.
Pleurotoma (Bathytoma) atractoides, Watson.
Pleurotoma (Genota) atractoides, Watson, Gasteropoda ‘ Challenger ’
Expedition, p. 501, pl. xx. fig. 8 a-c.
Bathytoma atractoides, Harris, Cat. Austral. Ter. Moll. parti. p. 49.
Bay of Bengal and the Arabian Sea. 459
Hab. Philippine Islands, 375 fath. (‘Challenger’) ; Stations
off Andaman Islands, 185-405 fath. (‘ Investigator’) ; in
188 fath. (Sowerby, P. Malac. Soe. i. p. 38).
The specimens from the Andaman Islands are perhaps a
trifle shorter in proportion to their width than the type and
have the transverse lire upon the body-whorl more distinctly
granose. A single oblique fold, not noticed by Watson, is
present upon the middle of the columella. This is only
visible when the outer lip is broken away. A very fine
example from 405 fath. is much larger than the specimen
obtained by the ‘ Challenger,’ being 47 mm. in length and
20 in width. Three out of the four examples examined have
a number of fine lire within the outer lip, a feature not
present in the ‘ Challenger’ shell.
P. Wetherelli, Kid., of the London Clay, and the Miocene
P. cataphracta are very closely allied forms.
From P. Oldhami this species differs in the absence of the
channelled suture and the broad raised belt with a deep
groove beueath it.
Pleurotoma (Bathytoma) Oldhami, Smith.
Pleurotoma (Bathytoma) Oldhamt, Smith, Ann. & Mag. Nat. Hist.
1899, vol. iv. p. 238; Illust. Zool. ‘ Investigator,’ pl. ix. figs. 2, 2 a.
Hab. Station 229, off Travancore coast, in 360 fath.
Pleurotoma (Ancistrosyrinz) travancorica, Smith,
var. granulata.
Pleurotoma (Aneistrosyrine) travancorica, Smith, Ann. & Mag. Nat,
Hist. 1896, vol. xviii. p. 368; Illust. Zool. ‘ Investigator,’ Mollusca,
pl. vil. figs. 1, La.
Hab. Station 229, off Travancore, in 360 fath.; Stations
233 and 240, off Andaman Islands, in 185-194 fath.
Three specimens from off Travancore differ from the type
in having the lower part of the body-whorl covered with
oblique rows of minute granules, also in having a spiral
liration in the concavity of the whorls near the dentate keel.
This liration bears small tubercles connected by short cross-
ridges with the dentations of the keel. Two examples from
the latter locality have the dentations at the angle of the
whorls conspicuously upturned, so that the upper part of the
volutions is deeply concave. The latter are twelve in number,
of which the apical one is smooth and globular.
460 Mri, A Salith on Wfollusoa Vrame the
Drillia investigatoris, Smith.
Drillia investigatoris, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv.
p- 240; Illust. Zool. ‘ Investigator,’ pl. x. figs. 1, la.
Hab, Station 233, off Andaman Islands, in 185 fath.
Drillia fugata, Smith.
Driliia fugata, Smith, Ann. & Mag. Nat. Hist. 1895, vol. xvi. p. 4,
pl. 1. figs. 5, 5 a.
Hab. Off Andaman Islands, in 405 fath.
A single specimen agreeing with the variety fig. 5 a.
Drillia captiva, Smith.
Drillia captiva, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 240;
Illust. Zool. ‘Investigator,’ pl. x. fig. 2.
Hab. Station 233, off Andaman Islands, 185 fath.
Drillia capta, Smith.
Drillia capta, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 240 ;
Illust. Zool. ‘ Investigator,’ pl. x. fig. 3.
Hab. Station 233, off Andaman Islands, 185 fath.
Drillia Worthingtoni, sp. n.
Testa breviter fusiformis, fuscescenti-albida; anfractus 9, duo
apicales leves, rotundati, ceteri superne excavati, infra nodose
costati (costis in anfr. penult. 8-10) et transversim tenuissime
striati, ultimus varice conspicuo rotundato ad sinistram instructo,
inter varicem et labrum haud costatus ; apertura parva; labrum
tenue, supra late et subprofunde sinuatum ; columella rectiuseula,
callo tenui, supra prope sinum subnodoso, induta.
Longit. 16 mm., diam. 6; apertura 6 longa, 2 lata.
Hab. Station 240, off Andaman Islands, in 194 fath.; off
Ross Island, 265 fath.
The lines of growth are fine and flexuous, and the fine
spiral striz only occur upon the lower half of the whorls,
the concavity above exhibiting only the sinuated incremental
lines.
Clathurella perlissa, sp. n.
Testa ovato-fusiformis, nitida, fuscescens, zona pallida infra suturam
aliaque circa medium anfr. ultimi ornata; spira turrita, acumi-
nata; anfractus 9, superiores 3, protoconcham constituentes,
leeves, primus convexus, duo sequentes infra medium carinati,
ceeteri (normales) supra decliviter excavati, infra conyexi, circa
Bay of Bengal and the Arabian Sea. 461
medium costati, costis bituberculatis, in anfr. penultimo 10, in
ultimo labrum versus obsoletis haud infra medium productis,
ultimus antice contractus et oblique striatus; apertura parva,
contracta ; labrum incrassatum, varicosum, album, ad suturam
sinuatum, intus denticulis 7-8 instructum, sed supra marginem
acutum minutius crenulatum ; columella alba, serie tuberculorum
minutorum munita; canalis anterior obliquus, mediocriter
angustatus.
Longit. 112 mm., diam. 53; apertura cum canali 6 longa, intus
13 lata.
Hab. Station 237, off Andaman Islands, 90 fath.
A very pretty glossy species. The costz are traversed by
two spirals producing a tuberculated appearance. Of the
very small tubercles upon the columella a few at the upper
or posterior part are more prominent than the rest.
Clathurella rugidentata (Sowerby).
Pleurotoma (Clathurella?) rugidentata, Sowerby, Proc. Malac. Soc.
vol. i. p. 38, pl. iv. fig. 11.
Hab. Station 240, off Andaman Islands, 194 fath. (‘ In-
vestigator’) ; in 188 fath. (Sowerby).
Besides the oblique slender costz and the fine spiral lire,
nodulous at the points of intersection, the surface exhibits
fine spiral raised striz in the interstices.
Trophon tenuirostratus, Smith.
Trophon tenuirostratus, Smith, Ann, & Mag. Nat. Hist. 1899, vol. iv.
p. 241; Ilust. Zool. ‘ Investigator,’ pl. x. figs. 4, 4a.
Hab. Station 2338, off Andaman Islands, in 185 fath.
Trophon indicus, Smith.
Trophon indicus, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 241 ;
Ilust. Zool. ‘ Investigator, pl. x. figs, 8, 5a.
Hab. Station 233, off Andaman Islands, in 185 fath.
Fusus captivus, Syith.
Fusus captivus, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 242 ;
Illust. Zool. ‘ Investigator,’ pl. x. figs. 8, 8 a.
Hab. Station 233, off Andaman Islands, 185 fath.
Murex ternispina, Lamarck.
Murex ternispina, Lamk., Kiener, Icon. Coq. Viv. p. 6, pls. vill, ix.,
fig. 1
g.
Hab. Twenty-six miles W.S.W. of Honawar, west coast of
462 Mr. E. A. Smith on Mollusca from the
India, in 28 fath.; off Mangalore, in 26-80 fath.; off south
coast of Ceylon, 34 fath. ; Station 237, off Andaman Islands,
90 fath.
Some variation exists among the series of specimens from
these localities ; those from off Honawar have the principal
spiral ridges dotted with red and only very slightly tubercu-
lated, whereas the examples from off Ceylon exhibit more
distinct tubercles and no dotting, but instead a very faint
brownish or reddish zone around the base of the body-whorl.
The apical portion of the spire is also more produced and the
sculpture of the first three normal whorls rather different.
They are more rounded and more finely cancellated.
Murex Troscheli, Lischke.
Murex Troscheli, Lischke, Jap. Meeres-Conch. i. p. 41, pl. i. figs. 1,2;
ii. pp. 29, 164.
Hab. Station 237, off Andaman Islands, 90 fath., stones.
The largest specimen is 110 mm. in length. This is small
in comparison with the type from Nagasaki, yet the shell
appears to be mature. The spines also are rather longer
and more slender. The whorls are rufo-lineated, but the
spines are more slender and longer than as shown in Lischke’s
figures. Pilsbry* has pointed out a similar variation in
Japanese specimens.
Murex mindanaensis, Sowerby.
Murex mindanaensis, Sowerby, Proc. Zool. Soc.-1840, p. 139.
Murex mindanaoensis, id. Conch. Ill. fig. 92, sp. 17; Thesaurus, iv,
pl. 381. fig. 21.
Murex mindensis, Reeve, Conch. Icon. fig. 78.
Murex mindanensis, Kobelt, Conch.-Cab. p. 111, pl. xxxiv. fig. 8.
Hab. Off Mangalore, Malabar coast, 26-30 fath.
One specimen only, rather young, 40 millim. in length.
; t San te ae - : eT oidei is
The type was originally described from the Philippine Islands.
Murex axicornis, Lamarck.
Hab. Station 237, off Andaman Islands, 90 fath.; off
south coast of Ceylon, 34 fath.
The Andaman examples are quite typical, as represented
by Kiener’s figure (Icon. Coq. Viv. pl. xlu. figs. 2), but
those from Ceylon have shorter spines and generally three
instead of two nodulous costz between the varices.
* Cat. Marine Moll. Japan, p. 41.
Bay of Bengal and the Arabian Sea. 463
Murex aculeatus, Lamarck.
Hab. Off south coast of Ceylon, 34 fath. (‘ Investigator ’) ;
Tizard Bank, China Sea, 20 fath. (H.M.S. ‘Rambler,’ in
Brit. Mus.).
The specimens from the above localities more closely agree
with Kiener’s figure (Coq. Viv. pl. xxxix. figs. 3) than with
the shell depicted by Reeve (Conch. Icon. vol. iii. fig. 60).
They have a single intermediate tubercle or plication between
the varices, and exhibit some transverse fine reddish lines, as
shown in Kiener’s figure. On the other hand, Reeve’s shell
has two intervening plice and only faint traces of the spiral
lineation.
Phos roseatus, Hinds.
Phos roseatus, Hinds, Voy. ‘Sulphur,’ Zool. vol. ii. p. 38, pl. x. figs. 9,
10; Sowerby, Thesaurus, vol. ili. p. 90, pl. cexxi. figs. 1-3; Tryon,
Man. Conch. vol. iii. p. 217, pl. Ixxwili. figs. 508-9.
Hab. Off south coast of Ceylon, 34 fath.
A more slender and more finely sculptured form than that
figured by Tryon and Sowerby. ‘The species occurs at
Sumatra, the Philippines, Moluccas, &c.
Nassaria suturalis (A. Adams).
Hindsia suturalis, A. Adams, Proc. Zool. Soc. 1853, p. 183; Kobelt,
Conch.-Cab., Purpuracea, p. 518, pl. Ixxvii, figs. 11, 12.
Nassaria suturalis, Sowerby, Thes. Conch. vol. ii. p. 86, pl. cexx.
figs. 15, 16; Tryon, Man. Conch. vol. iii. p. 221, fig. 542 (acwmi-
nata, part.).
Hab. Off south coast of Ceylon, 34 fath., and eight miles
south of Puri, Bengal, 13 fath. (‘Investigator’) ; Malacca
(A. Ad.) ; Ceylon (Layard).
N. bitubercularis, A. Adams, from Sorsogon, Philippine
Islands, is a synonym.
Nassaria nodicostata (A. Adams).
Hindsia nodicostata, A. Adams, Proc. Zool. Soc, 1853, p. 183 ; Kobelt,
Conch.-Cab., Purpuracea, p. 322, pl. Ixxvii. fig. 13.
Nassaria nodicostata, Sowerby, Thes. Conch. vol. iii. p. 86, pl. ccxx.
fig. 13.
Hab. Station 239, off Andaman Islands, in 55 fath. (‘ In-
vestigator ’) ; ? (A. Adams).
This so-called species is probably only a small variety of
N. acuminata, Reeve, from China, with which it has been
united by Tryon * together with half a dozen other species.
* Man. Conch. vol. iii. p. 221, fig. 546.
464 Mr. E. A. Smith on Mollusca from the
Nassaria nivea (Gmelin).
Buccinum niveum, Gmelin, Syst. Nat. p. 5495, non p. 3504.
Triton niveus, Reeve, Conch. Icon. vol. ii. sp. 75.
Hab. Gulf of Martaban, 6-100 fath., and off Vizagapatam
coast, 20 fath.
Found also at Tranquebar, Malacca, Ceylon, &c.
Nassaria levior, Smith.
Nassaria levior, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 242 ;
Illust. Zool, ‘ Investigator,’ pl. x. figs. 6, 6 a.
Hab. Station 237, off Andaman Islands, 90 fath.
Nassa gemmulata, var.
Buccinum gemmulatum, Lamarck, Kiener, Icon. Coq. Viv. p. 85, pl. xxii.
fig. 84.
Nassa gemmulata, Reeve, Conch. Icon, vol. viii. fig. 29.
Var.= N. variegata, A. Adams, Reeve, J. c. fig. 70.
Hab. Off Mangalore, Malabar coast, 26-30 fath.
The specimens from the above locality belong to the small
finely granose form of this species named variegata by
A. Adams. Buccinum conoidale, Deshayes, also, as suggested
by Tryon, appears to belong to this species. N. verrucosa,
A. Adams, is another variety.
Nassa crenulata (Bruguiére).
Nassa crenulata, Bruguitre, Reeve, Conch. Icon, vol. viil. figs. 2 a, 2 6.
Hab. Lat. 18° 17'N., long. 93° 7! E., off Andaman Islands,
90 fath.
Nassa aracanensis, Smith.
Nassa aracanensis, Smith, Ann. & Mag, Nat. Hist. 1899, vol. iv. p. 243;
Illust. Zool. ‘ Investigator,’ pl. xi. figs, 2, 2 a.
Hab. Reef Island, Kyuk Phyon, off Aracan coast.
Nassa diluta, Smith.
Nassa diluta, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 248 ;
Ilust. Zool. ‘ Investigator,’ pl. xi. figs. 3, 3a.
Hab. Off Colombo, 597 fath.; also off Kistna coast, 753
fath.
Metula Hindsi, H. & A. Adams.
Buecinum metula, Hinds, Voy. ‘Sulphur, p. 31, pl. xvi. figs. 13, 14
Tryon, Man. Conch. vol. iii. p. 153, pl. bexil. fig. 240.
Bay of Bengal and the Arabian Sce. 465
Buccinum mitrella, Adams & Reeve, Voy. ‘Samarang, Zool., Moll.
p. 32, pl. xi. fig. 13; Tryon, op. cit. p. 152, pl. Ixxil. fig. 2389 (as
Metula).
Hab. Off Coromandel coast, 41 fath.
Buccinum mitrella was originally described from the China
Sea. The single specimen obtained by the ‘ Investigator ’ is
larger than the type, being 24 mm. in length and 7 in width.
The whorls also are slightly more convex. A feature not
referred to in the description is the presence of varices at
intervals up the spire, being merely the slightly thickened
former outer lips of the aperture.
A careful examination of the description and figures given
by Hinds of his Buccinwm metula and a comparison of speci-
mens in the Cuming collection apparently indicate that that
species and Buccinum mitrella belong to the same form,
differing only in size. The examples of B. metula in the
British Museum are quite as small as that figured in the
‘Sulphur,’ and, with the exception of size, are undistinguish-
able from the larger form mitrella. Hinds’s locality, “ West
coast of Veragua,” may be an error.
Tritonidea delicata, Smith.
Tritonidea dehicata, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 242;
Illust. Zool. ‘ Tuvestigator,’ pl. x. figs. 7, 7 a.
Hab. Station 237, off Andaman Islands, 90 fath.
Pisania angusta, Smith.
Lisania angusta, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 243;
Tlust. Zool. ‘ Investigator,’ pl. xi. figs. 1, 1 a.
Had. Off south coast of Ceylon, 34 fath.
Columbella (Mitrella) supraplicata, Smith.
Columbella (Mitrella) supraplicata, Smith, Ann. & Mag. Nat Hist.
1899, vol. iv. p. 244; Ilust. Zool. ‘ Investigator,’ pl. xi. figs. 7, 7 a.
Hab. Station 232, off Travancore coast, in 430 fath.
Columbella (Meta) philippinarum, Reeve.
Hab. Station 237, off Andaman Islands, 90 fath. (¢ In-
vestigator ’) ; Philippine Islands (Reeve) ; N. Borneo (Ussher
& Everett, in Brit. Mus.).
The ‘Investigator’ specimens, coming from deep water,
have lost almost all the colour-markings which usually are
present in this species. They are dirty white, with just
466 Mr. E. A. Smith on Mollusca from the
feeble traces of brown zigzag lines and wavy longitudinal
lineation. ‘Two specimens in the Museum collection, collected
in shallow water at the Andamans by Lieut. A. W. King
and Capt. Francis Hamilton, have much brighter markings.
Latiaxis diadema (A. Adams).
Murex diadema, A. Adams, Proce. Zool. Soc. 1853, p. 70.
eee diadema, Sowerby, Thes. Conch. vol. v. p. 2, pl. eccexxiv.
era:
Hab. Off south coast of Ceylon, 34 fath. (‘ Investigator”) ;
Philippines (A. Ad.); Mauritius (Robillard, in Brit. Mus.).
The type of this species has been so overcleaned that the
very beautiful transverse sculpture is almost obliterated. It
consists of very numerous fine lire, which are minutely
squamose and undulating. The two specimens from Ceylon
are of a delicate rose tint within the aperture and have a
series of flattened hollow spines upon the lower angle of the
body-whorl. They do not curve upwards like those above,
but stand out horizontally. The columella is coated with an
erect pink callus which unites with the labrum above.
A specimen from Mauritius obtained by the late Victor
Robillard is larger than the typical form and differs also in
being totally white, and the second keel upon the body-whorl
is ornamented with very numerous hollow, short, somewhat
upceurved spines. Also between this series and the squamose
crest at the base there is another series of smaller scale-like
spines. The fine, delicate, transverse sculpture which covers
the entire surface is of the same character as in the other
examples.
Length 36 mm.
19. Coralliophila indica, Smith.
Coralliophila indica, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv.
p- 244; Illust. Zool. ‘Investigator, pl. xi. figs. 8, 8 a.
Hab, Station 232, off South India, 430 fath.
Cancellaria trigonostoma, Lamarck.
Hab. Off Coromandel coast, in 41 fath.
The single small example differs from the typical form in
having more distinct longitudinal plice and finer spiral striae,
the surface of the body-whorl being minutely reticulated. It
consists of four normal and two and a half apical whorls, the
latter being smooth and convex.
Bay of Bengal and the Arabian Sea, 467
Cancellaria paucicostata, Sowerby.
Cancellaria paucicostata, Sowerby, Proc. Malac. Soe. vol. i. p. 160,
pl. xii. fig. 26.
Testa angulatim ovata, imperforata, dilute fuscescens, oblique
costata et transversim tenuiter subgranose lirata; anfractus 5,
celeriter crescentes, supremi duo leves, convexi, tertius cancel-
latus, penult. costis circiter 16 instructus, ultimus supra medium
obtuse angulatus, costis circa 8-10 sensim magis distantibus
ornatus ; apertura irregulariter triangularis, alba, longit. totius 2
superans, antice leviter canaliculata; labrum incrassatum, intus
tenuiter liratum ; columella arcuata, triplicata, callo tenui induta.
Longit. 17 mm., diam. 13, apertura 10 longa, 7 lata.
Hab. Off south coast of Ceylon, 34 fath. (‘ Investigator ’) ;
Persian Gulf (Sowerby).
The transverse liree are very fine and alternately larger
-and smaller, and, being crossed by the lines of growth, have
a very pretty subgranose appearance.
The type of this species in the British Museum is of a
very pale reddish tint with a narrow whitish line round the
middle of the body-whorl and another at the angulation
above. In the Ceylonese specimen these pale zones are only
just traceable. The lire within the labrum are about
seventeen in number.
Cancellaria cretacea, Smith.
Cancellaria cretacea, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iy.
p- 245; IIlust. Zool. ‘ Investigator,’ pl. x1. figs. 5, 5a.
Hab. Station 229, off Travancore coast, in 360 fath.
Ancilla leucospira, Smith.
Ancilla leucospira, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 245;
lust. Zool. ‘ Investigator,’ pl. xi. figs. 4, 4a.
Hab. Station 240, lat. 11° 32! N., long. 92° 46! K., off
Andaman Islands, 194 fath,.
Ancilla glans, Smith.
Ancilla glans, Smith, Ann, & Mag. Nat. Hist. 1899, vol. iv. p. 246;
Illust. Zool. ‘ Investigator,’ pl. xi. figs. 6, 6 a.
Hab. Station 233, off Andaman Islands, 185 fath.
Ancilla Tindalli, Melvill.
Ancilla Tindalli, Melvill, Mem. & Proc. Manchester Lit. & Phil. Soe.
1898, vol. xlii. pt. ii. p. 14, pl. i. fig. 1.
Hab. Off south coast of Ceylon, 34 fath.
468 Mr. E. A. Smith on Mollusca from the
A single example agreeing in all respects with the type
from the Angrias Bank, west of Bombay.
Marginella angustata, Sowerby.
Hab. Off Coromandel coast, 41 fath.
The specimens from this locality are much smaller than the
types figured by Sowerby, the average length being only
13-14 mm. ‘They differ also in exhibiting a small spire
consisting of a few whorls, which, in the large form, becomes
concealed by callus.
Marginella grisea (Jousseaume).
Persicula grisea, Jousseaume, Rev. Mag. Zool. 1875, p- 268.
Marginella obtusa, Sowerby, Proc. Zool. Soc. 1870, p. 254; non M. ob-
tusa, Sow., 1846.
Marginella sexplicata, Dunker, ubi?; Weinkauff, Conch.-Cab. ed. 2,
p. 85, pl. xvi. figs. 6, 7.
Hab. Gulf of Martaban, 67 fath.
It seems to me doubtful whether the shell figured by
Weinkauff is the same species as that described by Sowerby.
The type of obtusa in the British Museum is much larger
(24 mm.) and narrower, has a flatter spire, and the plicee
on the columella seem different. I have been unable to find
any reference to this species by Dunker before the year 1882
in his ‘ Index Moll. Maris Japon.’ p. 57. The quotation by
Weinkauff “ Mus. Godeffr. Cat. 3 (1871)” is evidently
erroneous, as that Catalogue was issued in 1866. Tryon,
in his monograph of this species (Man. Conch. vol. v.), has
merely followed Weinkauff, giving the same reference to the
Godeffroy Catalogue ; and Pilsbry also (Cat. Marme Moll.
Japan, p. 24) throws no light upon the point.
Turritella fascialis, Menke.
Turritella fascialis, Menke, Kobelt, Conch.-Cab. ed. 2, p. 13, pl. aye
fig. 5.
Hab. Off south coast of Ceylon, 34 fath.
Undistinguishable from Japanese examples.
Turritella columnaris, Kiener.
Turritella columnaris, Kiener, Kobelt, op. cit. p. 48, pl. v. figs. 1, 2.
Hab. Off Mangalore, Malabar coast, 26-80 fath.
Bay of Bengal and the Arabian Sea. 469
Strombus Listeri, T. Gyay.
Buccinum Bilingue canadense, Lister, Hist. Conch. pl. 855. fiz. 12 a.
Strombus Listeri, T. Gray, Ann. & Mag. Nat. Hist. 1852, vol. x.
p- 4380; Tryon, Man. Conch. vol. vii. p. 114, pl. iv. fig. 45.
Besomebus mirabilis, Sowerby, Proc. Zool. Soc. 1870, p. 257, pl. xxi.
fig.
Hab. Ceylon (Sowerby) ; Gulf of Martaban, in 67 fath.
(‘ Investigator ’).
Only two young examples were obtained by the ‘ In-
vestigator, but the record of another locality is interesting.
They consist of ten normal and three nuclear whorls, the
latter being globose, smooth, and glossy. At this age, before
the last whorl is formed, the shell is fusiform and the
columella almost straight. The ground-colour is white,
variegated with numerous undulating, somewhat zigzag,
brown flames. The last whorl is obliquely grooved upon the
lower or anterior part.
Strombus Sibbaldi, Sowerby.
Strombus Sibbaldii, Sowerby, Thesaurus Conch. vol. i. p. 28, pl. vi.
figs. 10,11; Reeve, Conch. Icon. vol. vi. pl. xviii. fig. 48.
Hab. Off south coast of Ceylon, 34 fath.; also off Coro-
mandel coast, 41 fath.
A small, but apparently adult, shell from the latter locality
is destitute of colour-marking, and only 27 mm. in length.
Rostellaria Powisii, Petit.
Rostellaria Powisi?, Petit, Mag. de Zool. 1842, pl. liii.
Hab. China (Petit and others) ; Gulf of Martaban, in 67
fath. (‘Investigator’).
This species, which is figured in the monographs by
Sowerby, Reeve, Kiener, Kiister, and Tryon, appears to have
hitherto been recorded from China only. Its occurrence in
the Indian Ocean is therefore of some interest.
Xenophora (Haliphebus) solaris (Linn.).
Hab. Off Ganjam coast, in 28-30 fath. (‘ Investigator’) ;
Coromandel and Nicobars (Chemnitz) ; Malacca (Cuming).
Xenophora pallidula, Reeve.
Hab. Off Andaman Islands, in 185 fath., and off Tavancore
coast in 860 fath. (‘ Investigator’) ; Japan (Reeve, &c.)
Ann. & Mag. N. Fist. Ser. 7. Vol. xiit. 32
s
470 Mr. E. A. Smith on Mollusca from the
Pirula gracilis, Sowerby.
Pirula gracilis, Sowerby, Smith, Journ. Malacol. vol. ii. p. 67.
Pyrula Dussumieri, Kiener, Smith, Ann. & Mag. Nat. Hist. 1894,
vol. xiv. p. 164.
Hab. China Sea (Kiener, &c.); Station 69, in 20 fath.
(‘ Investigator ’).
Ranella (Biplex) perca (Perry).
Hab. Station 240, off Andaman Islands, 194 fath.
Ranella bituberculata, Lamarck.
Hab. Off Mangalore, Malabar coast, 26-30 fath.
Distortriz cancellinus (Roissy).
Hab. Station 237, off Andaman Islands, 90 fath.; off
Ganjam coast, 28-30 fath.; also 8 miles south of Puri,
13 fath.
Lotorium tripus, Lamarck.
Hab. Off south coast of Ceylon, 34 fath. ; also off Malabar
coast, 28 fath.
Ovula bullata, Adams & Reeve.
Ovulum bullatum, Adams & Reeve, Voy. ‘Samarang,’ Moll. p. 28,
pl. vi. figs. 13a, 6; Reeve, Conch. Icon. vol. xv. pl. vi. figs. 26 a, b;
Sowerby, Thesaurus, vol. ii. pl. ci. figs. 95, 96; Weinkauff, Conch.-
Cab. ed. 2, p. 187, pl. xlviii. figs. 5 & 8.
Calpurnus bullatus, A. Adams, Journ, Linn. Soc., Zool. 1864, vol. vii.
p- 95.
Hab. Off south coast of Ceylon, 34 fath. (‘ Investigator’);
Singapore (Ad. & Reeve); Japan (A. Ad.).
Two specimens exactly like the type, the larger being
103 mm. in length.
Radius Angasi (Reeve).
Ovulum Angasi (Adams MSS.), Reeve, Conch. Icon. vol. xy. pl. x.
figs. 43 a-6.
Hab. Off south coast of Ceylon, in 34 fath. (‘ Investigator’);
Port Curtis, Queensland (Reeve).
Two specimens of a very pale rose tint, with the two
extremities tipped with brown. ‘The latter feature is faintly
present in the type, although not referred to by Reeve. Both
the anterior and posterior ends are obliquely striated dorsally.
The ventral part of the body-whorl is rather more humpy in
the Australian form than in those from Ceylon.
Bay of Bengal and the Arabian Sea. 471
Trivia producta (Gaskoin).
Cyprea producta, Gaskoin, Reeve, Conch. Icon. vol. ili. pl. xxiv.
figs. 137 a, 6; Sowerby, Thes. Conch. vol. iy. p. 49, pL. 827. figs. 495,
A96.
Hab. Off Coromandel coast, 41 fath. (‘ Investigator ’) ;
Agulhas Bank, 8. Africa (Sowerby) ; Red Sea (Weinkauff) ;
Borneo, Australia (Tryon).
Trivia pisum (Gaskoin).
Cyprea pisum, Gaskoin, Sowerby, op. cit. p. 44, pl. 326. figs. 448, 449.
Hab. Off south coast of Ceylon, 34 fath.
Scala Kienert (Canefri).
Cirsotrema Kieneri, Canefri, Journ. de Conch. 1876, p. 155.
Scalaria decussata, Kiener, non Lamarck, Icon, Coq. Viv. p. 21, pl. vii.
fig. 23; Sowerby, Thes. Conch. vol. i. p. 105, pl. xxxy. tig. 140.
Amea Sowerbyi, Dunker, Index Moll. Mar. Jap. p. 69.
Scala fimbriolata, Melvill, Mon. Manchester Phil. Sec. 1897, vol. xli.
pe tly vol. xi. pl. 1. fig. 12.
Hab. Of south coast of Ceylon, 34 fath. (‘ Investigator ’):
other localities are :—Arabia (Sowerby) ; Japan (A. Adams,
Dunker, Pilsbry) ; Mekran coast (Melvill); Darnley Island,
N. Australia (Mus. Cuming).
T am inclined to believe that Tryon is right in considering
the S. decussata of Sowerby the same as that figured by
Kiener under that name. After carefully comparing the
type of S. fimbriolata, a young shell, with this species, I have
failed to find any distinguishing characters. .
The shell described by Clessin* as a new species, under
the name of S. Sowerby, is quite distinct from the present
form.
Scala multiperforata (Sowerby).
Scalaria multiperforata, Sowerby, Conch. Icon. vol. xix. pl. xvi.
fig. 125.
Hab. Off south coast of Ceylon, 34 fath. (‘ Investigator ’) ;
Mauritius (Sowerby).
A single large dead specimen, 40 mm. in length. It is
doubtful whether this species is separable from S. cochlea,
Sowerby, said to be from West Africa.
Scala subcasta (Smith).
Scalaria subcasta, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv. p. 246;
Illust. Zool. ‘ Investigator,’ pl. xii. figs. 2, 2 a.
Hab. Station 232, off Travancore coast, 430 fath.
* Conch,-Cab, ed. 2, p. 63, pl. xv. fig. 1.
472 On Mollusca from the Bay of Bengal &e.
Scala bengalensis (Smith).
Scalaria bengalensis, Smith, Ann. & Mag. Nat. Hist. 1899, vol. iv.
p. 246; Ilust. Zool. ‘ Investigator,’ pl. xii. figs. 1, 1 a.
Hab. Station 229, off Travancore coast, in 360 fath.
Lacuna indica, Smith.
Lacuna indiea, Smith, Ann. & Mag. Nat. Hist, 1894, vol. xiv. p. 165,
pl. iv. fig. 7.
Hab. Off Kistna coast, 753 fath.
The shell is white beneath an excessively thm deciduous
epidermis, which produces the “ sordide albida”’ appearance,
as described in the original diagnosis.
Lacuna globosa, sp. 2.
Testa globosa, tenuis, anguste umbilicata, pellucido-alba, peri-
ostraco-tenuissimo induta, limo rufescente seepe inerustata, lineis
incrementi sculpta ; anfractus quatuor, celeriter acerescentes,
perconvexi, ultimus antice oblique descendens, inferne circa
umbilicum carina prominente gracili instructus; apertura irregu-
lariter rotundata; peristoma tenue, continuum, margine externo
infra late sed haud profunde sinuato, columellari in medio leviter
reflexo et sinuato; operculum corneum, paucispirale, anfractibus
3—4 constructum.
Diam. maj. 5 mm., min. 4, alt. 5.
Hab. Station 212, in 111 fath.
Within the aperture a narrow and shallow groove corre-
sponds with the external umbilical keel. Just above the
termination of the latter the peristome exhibits a broad but
shallow sinus. I regret being unable at present to give the
position of Station 212.
Natica rufa, Born.
Natica rufa, Smith, Ann. & Mag. Nat. Hist. 1894, vol. xiv. p. 165,
pl. iv. figs. 14, 14a.
Hab. Bay of Bengal, 65 fath.
A single specimen with rather higher spire than usual.
Natica violacea, Sowerby.
Natica violacea, Philippi, Con.-Cab. ed. 2, p. €6 bis, pl. x. fig. 18.
Hab. Off Andaman Islands, 15 fath. (‘Investigator ’);
other localities are Philippines, Fiji, Manritius.
No description of the operculum appears to have been
oo
Bibliographical Notices. 47%
published, excepting that Sowerby, in the original diagnosis *,
mentions that it is testaceous. It is white, glossy, and
slightly concave externally, with a groove and a ridge
parallel with the outer curved margin, whilst the straight or
columellar side is finely serrate. Parallel with the curved
outline may be noticed numerous faint subpellucid lines
which arise between the denticles on the serrated edge.
[To be continued. ]
BIBLIOGRAPHICAL NOTICES.
Memoirs of the Geological Survey of the United Kingdom.—The
Cretaceous Rocks of Brituin. Vol. III. The Upper Chalk of
England. By A. J. Juxes-Browne. With Contributions by
Witiam Hirt, F.G.8. 8vo. Pp. x and 566. With 79 Illus-
trations in the text and 1 Plate. 1904. E. Stanford, London ;
J. Menzies, Edinburgh; and Hodges & Co., Dublin. Price 10s.
As in the case of Vol. II. of this work (noticed in the Ann. & Mag.
Nat. Hist. for February 1904), the Board of Agriculture and
Fisheries, desirous that agriculturalists and others should have full
benefit, has distributed this volume also for review.
The Memoirs of the Geological Survey of the United Kingdom
always bring together much valuable material, and this volume is
in no way wanting in this respect. ‘The Upper Chalk is defined by
the authors as consisting of the zones of Holaster planus, Micraster
cor-testudinarium, Micraster cor-anquinum, Marsupites, Actinocamax
quadratus, Belemnitella mucronata, and Ostrea lunata. The zonal
divisions of the Chalk are fully recognized in this volume, although
the authors seem reluctant to part with the obsolete divisions of
“Upper,” “Middle,” and ‘ Lower,’ which have now such small
significance. They also seem to hanker after a fresh system of
zonal nomenclature (p. 5), but this seems to us to be unnecessary.
In the descriptions of the coast-sections full credit is given to
Dr. Rowe, who must certainly feel rewarded in reading the generous
tribute to his work in the Preface by the Director. Indeed it is
quite clear, and is so stated (p. 38), that the publication of Messrs.
Rowe and Sherborn’s work necessitated the re-writing of those
parts of this Memoir which deal with the districts that they have
examined; and this is the more clearly brought out at pp. 275-278
(‘‘ Yorkshire”), if anyone will take the trouble to compare the
official account with that recently published by Dr. Rowe in the
* Proceedings’ of the Geologists’ Association. It is more and more
evident that future work in the field must be conducted by those
who have more than a working knowledge of the zoology of the
beds which they are surveying, as the exactitude of results achieved
* Tankerville Cat. p. xi.
A474 Bibliographical Notices.
of late years in the Silurian, Carboniferous, and Chalk rocks has
amply demonstrated.
After the description of each coast-section, the authors deal in
detail with the inland exposures, and collect together a mass of
information which should prove extremely valuable when a zonal
survey of Counties is undertaken. That this must come in the
near future is evident by a recent attempt by Mr. Jukes-Browne
himself to indicate the zones in the Chalk of Suffolk from fossils
collected in pits. In the description of the Norfolk coast, Mr. Jukes-
Browne establishes a new zone, the zone of Ostrea lunata, on the
collections of Messrs. C. Reid and R. M. Brydone: the results
obtained by the latter were published in 1900. It is comforting to
be reminded that there is a certain amount of this interesting zone
inland, as shown by the Well at Mundesley, since the northern
shore-mass of Junata Chalk at Trimingham is almost worn away.
Chapter xxi. is devoted to a sketch of the Upper Chalk of
France, wisely inserted for comparison. Chapter xxil.. (pp. 302-
353), dealing with the microscopical characters of the Chalk, by
Mr. Hill, is a summary, with additions, of his well-known papers on
the subject. The author is indebted to Mr. F, Chapman (now of
Melbourne) for determining the Foraminifera and Ostracoda (p. iv).
A discussion of the chemical composition of the Chalk occupies
Chapter xxiii. (pp. 8354-860). The bathymetric conditions and the
variations of the sea-bottom during the formation of the Upper
Chalk occupy Chapter xxiv. ; an account of the economic products,
Chapter xxv. (pp. 379-402); of the physical features, Chapter xxvi.
(pp. 402-424); and of the water-supply from the Chalk, Chapter
XXxvil. (pp. 425-446). One Appendix contains critical remarks on
some of the fossils, and gives a list of all the known fossils up from
the Upper Greensand (Selbornian) to the O. lunata zone, with
careful indications of the zonal succession. Appendix II. gives a
full Bibliography of publications relating to the rocks and fossils of
the Upper Cretaceous Series of England.
We congratulate the Officers of the Geological Survey and Messrs.
Jukes-Browne and Hill on having completed a very laborious and
tedious task. We wish we could do the same for the printers.
‘The paper seems better than usual, but there appears to be a difficulty
in keeping the type clean; while in two copies of this work that
we have seen the diagram at p. 206 is shorn of many of its letters.
There are a few editorial slips—e. g., Pecten serrat at p. 12. Many
of the woodcuts are too antiquated for current books ; such new
ones as that on p. 26 are indeed a long way “ after Rowe” ; and it
is puzzling to distinguish in the picture at p. 91 the special layers of
flint alluded to in the text.
Pictures of Bird-Life. By R. B. Lover.
London: Bousfield & Co. 1903.
Nownerg, perhaps, has the perfection of the camera and of photo-
graphic methods been more appreciated than among field-naturalists,
Miscellaneous. 475
Within the last few years there has arisen, in consequence, quite a
bewildering number of volumes, large and small, dealing with
animal life, and especially birds, all illustrated by photographs.
Many of these volumes have but little to recommend them: others
constitute standing monuments of infinite patience and laborious
research ; among these Mr. Lodge’s work will take front rank.
Mr. Lodge is not merely a photographer who finds birds con-
veniently useful subjects for the purpose of book-making ; on the
contrary, he is an ornithologist first and a photographer afterwards
—albeit a skilled photographer, as the pages of this volume testify.
Considerations of space forbid anything more than the merest
outline of the scope of this book or reference to anything more than
a few isolated facts to show the accuracy and value of the observa-
tions which render the text such delightful reading. The Author
commences with a chapter on bird-life in a suburban parish,
and then goes on to describe such easily accessible observation-
stations as the Lincolnshire mud-flats, the Norfolk broads, and the
Farne Islands. Next follows an account of his more ambitious
explorations in the Dutch marshes, the Spanish marismas, and the
fjords and forests of Denmark. Observations of real scientific value
occur plentifully throughout these pages. Less welcome, and
equally numerous, are painful references to the work of extermina-
tion which is proceeding apace throughout these islands. This is
due partly to the insensate greed of the collector, and partly to the
gross ignorance of the gamekeeper, who, in addition, and in spite of
laws for the prevention of cruelty to animals, is guilty of acts of
barbarity which can only be described as devilish. It is high time
that some more effective legislation was introduced for the suppres-
sion of these evils.
There are three chapters in this book which will prove very
acceptable to many, since they deal with the question of the
photographer’s outfit and automatic photography by electricity—
an extremely valuable aid in obtaining pictures of suspicious birds,
otherwise unapproachable.
There are over two hundred illustrations in this book, some of
which are of great beauty. The eight coloured plates are all
unusually good. The book is well bound, well printed, and a work
of which both author and publisher may feel proud,
MISCELLANEOUS.
Teleostome Phylogeny : a Correction.
I am indebted to Mr. Boulenger for kindly calling my attention to
a mistake in my paper on Teleostome phylogeny in the last number
of the ‘Annals. On page 3381, in the definition of the order
Dipneusti the word “not” should be omitted, thus reading ‘“ Clavicle
distinct from the cleithrum,”—C. Tare Regan,
476
INDEX to VOL. XIII.
ADELOCEPHALA, new species of, 242.
Acanthoclonia, new species of, 444.
Acanthomima, characters of the new
genus, 458.
Acis, new species of, 38].
Algathia, new species of, 222.
Anaxita, new species of, 242.
Anglas, J., on the relations between
the development of the tracheal
apparatus and the metamorphoses
of insects, 403.
Animals, on the
marine, 117.
Anomalurus, new subspecies of, 70.
Apatelodes, new species of, 246.
Aphanus, new species of, 355.
Apistocalamus, new species of, 451.
Arachnida, new, 695.
Araspus, characters of the new
genus, 112.
Arculanus, characters of the new
genus, 198.
Argenis, characters of the new genus,
107.
Armachanus, new species of, 202,
Arvicanthis dorsalis, new subspecies
of, 414.
Atractus, new species of, 451.
Attacus, new species of, 244.
Atyidee, on the mutations of certain,
O77.
Automolis, new species of, 241.
Bacillinz, definition of the new sub-
family, 450.
Bacteriine, definition of the new
subfamily, 451.
Bactricia, new species of, 429.
Bactriciinew, definition of the new
subfamily, 429.
Balantiopteryx, new species of, 252.
Barbus, new species of, 158, 190, 287,
449,
Barilius, new species of, 191.
Barrett-Hamilton, G. E. H., on an
undescribed weasel from the Atlas
distribution of
Mountains, 323; on new species
of Mustelidee, 588.
Batrachia, new, 42, 130, 261.
Beddard, F. E., on the anatomy of
Eryx and other Boida, 233.
Bell, A. M., on implementiferous
sections at Wolvercote, 328.
Bell, Prof. F. J., on a new genus of
Spatangoids, 236.
Bernard, H. M., on the prototheca of
the Madreporaria, 1.
Boide, on the anatomy of the, 235.
Books, new :—Oates and Reid’s
Catalogue of the Collection of
Birds’ Eggs in the British Mu-
seum, 76; Gordon’s The Geolo-
gical Structure of Monzoni and
Fassa, 77; Jukes-Browne’s The
Lower and Middle Chalk of Eng-
land, 158; Lankester’s Treatise on
Zoology, pt. i., 159; Murie’s Report
on the Sea Fisheries and Fishing
Industries of the Thames Estuary,
325; Lydekker’s Mostly Mammals,
395; Hampson’s Catalogue of the
Noctuide in the British Museum,
396; The Fauna of British India,
Rhynchota, vol. ii. pt.1., 897; Pa-
leontologia Indica, ser. ix. vol. i11.
pt. 2, 897; Circulars on Agricul-
tural Economic Entomology, 399 ;
Julkes-Browne’s The Upper Chalk
of England, 473 ; Lodge’s Pictures
of Bird-Life, 474.
Boulenger, G. A., on a new genus of
frogs, 42 ; on new frogs and snakes
from Yunnan, 130; synopsis of
the suborders and families of
Teleostean fishes, 161 ; on a new
Barbus from Cameroon, 237; on
two new genera of Ranide, 261;
on new species of Barbus from
Lake Victoria, 449; on three new
snakes, 450.
Bourgeois, J., on the Rhipidoceride
EINDUREX,
and Malacodermata in the Burchell
collections, 89.
Bouvier, E. L., on the genus Ort-
mannia and the mutations of
certain Atyids, 377.
Bulua, characters of the new genus,
262.
Burchell, W. J., on the collections
of, 45, 56, 89, 305, 356.
Butler, Dr. A. G., on African butter-
flies of the subfamily Pierine,
426,
Callula, new species of, 131.
Calman, Dr. W. T., on the classifica-
tion of the Crustacea Malacostraca,
144,
Calostylis, on the prototheca of, 1,
Calvisia, new species of, 435.
Cameron, P., on new hymenoptera
from Northern India, 211, 277.
Camptobrochis, new species of, 201,
274.
Candalides, new species of, 140.
Capellanus, characters of the new
genus, 109,
Carlisis, new species of, 350.
Carvilia, new species of, 85.
Cataulus, new species of, 452.
Cator, D., on new Lycznide from
Sierra Leone, 73.
Celetes, new species of, 93.
Centropomus, new species of, 260.
Cerceris, new species of, 292.
Cheetodon, new species of, 277.
Chamus, characters of the
genus, 197.
Characodon, new species of, 257.
Chlamydolycus, new species of, 91.
Clathurella, new species of, 460.
Clupea, new species of, 255.
Cockerell, T. D. A., on some para-
sitic bees, 55.
Ceelioxys, new species of, 215.
ribis, new variety of, 33.
Coleoptera, new, 91.
Colpoglossus, characters of the new
genus, 42.
Cricetomys, new species of, 412.
Crustacea Malacostraca, on the classi-
fication of the, 144.
Ctenucha, new species of, 241.
Cyphodema, new species of, 201.
Dagbertus, characters of the new
genus, 203.
Dandinus, characters of the new
genus, 264.
Davies, H. N., on the discovery of
new
4T7
human remains in Gough’s cavern,
400.
Depastrum cyathiforme, notes on,
62.
Diaphomerine, definition of the new
subfamily, 450.
Dieuches, new species of, 268,
Dircenna dero, note on, 317.
Distant, W. L., revision of the Cap-
sidee in the British Museum, 103,
194; on heteroptera from North
Queensland, 263; on a new genus
of Coreidz from Borneo, 303; on
heteroptera from the Transvaal,
349,
Dithmarus, characters of the new
genus, 593.
Drillia, new species of, 460.
Druce, H., on new heterocera from
S. America, 241.
Druce, H. H., on new Lycenide
from Borneo, 140.
Endochus, new species of, 355.
Engraulis, new species of, 255.
Eobrissus, characters of the
genus, 256.
Epeolus, synopsis of the genus, 31;
new species of, 39.
Eryx, on the anatomy of, 253.
Estuidus, characters of the new
genus, 272.
Eubulides, new species of, 441.
Eucerocoris, new species of, 271.
cumecopus, new species of, 265.
Eurycantha, new species of, 442.
Kurycenema, new species of, 439
Kustema, new species of, 248,
Felis ocreata and its subspecies, note
on, 421,
Fingulus, characters of the new
genus, 275.
Fishes, new, 135, 190, 237, 255, 260,
276, 449; synopsis of the sub-
orders and families of Teleostean,
161;
Francis, Dr. W., obituary notice of,
Aner
Fulgentius, characters of the new
genus, 105.
Fulton, F., on new species of Catau-
lus, 452.
Funisciurus congicus, new subspecies
of, 410.
Geocoris, new species of, 267,
Geological Society, proceedings of
the, 326, 399.
Geomorpha, new species of, 350,
new
Ann. & Mag. N. Hist. Ser. 7. Vol. xiii. 33
478 INDEX.
Germalus, new species of, 266.
Gnathoconus, new species of, 349.
Gonomeandrus chrysostephanus, note
on, 80.
Haaniella, definition of the new
generic name, 444,
Habropoda, new species of, 211.
Hadrojoppa, new species of, 278.
Halictus, new species of, 302.
Hapalopeza, new species of, 85.
Harpactor, new species of, 355.
Havinthus, new species of, 269.
Healey, Miss M., on some Upper
Jurassic Ammonites, 326.
Henderson, W. D., on new species of
Acis, 381.
Herdoniaria, characters of the new
division, 103.
Heros, new species of, 258.
Herpestes albicaudus, new subspecies
of, 408.
Heterocampa, new species of, 248.
Heterocheeta, new species of, 87.
Heteroptera, new, 103, 194, 268, 08,
349,
Hipposideros Commersoni, on the
subspecies of, 384.
Hoge, H. R., on a new genus of
spiders, 65,
Holocentrum osculum, description of,
259.
Horcias, new species of, 200.
Humbertiella, new species of, 83.
Hydrethiops, new species of, 450.
Hygrochroa, new species of, 248.
Hymenoptera, new, 838, 211, 277.
Tenacia, new species of, 446,
Insects, on the relations between the
development of the tracheal appa-
ratus and the metamorphoses of,
405.
Kennetus, characters of the new
genus, 303.
Kirby, W. F., on the Mantide in
the British Museum, 81]; on Phas-
mide in the British Museum, 372,
429,
Kirkpatrick, R., on medusee from
Japan, 80.
Lacuna, new species of, 472.
Larra, new species of, 294, 802.
Layeran, A., on the action of human
serum on certain pathogenic Try-
panosomes and the action of ar-
senious acid on Trypanosoma
gambiense, 401.
Lepidoptera, new, 73, 140, 241; on
the, collected by W. J. Burchell
in Brazil, 305, 356.
Lepus, new species of, 420.
Leucothyris phenomoe, new sub-
species of, 315.
Liobagrus, new species of, 193.
Liptena, new species of, 76.
Liris, new species of, 500.
Lonchodes, new species of, 873.
Linnberg, Dr. E., on fishes from the
Cameroon, 155,
Lonomia, new species of, 247.
Lyceenidee, new, 73, 140.
Lycorea halia, note on, 859.
Lygus, new species of, 199, 273.
australis and L. zthiops, defi-
nition of the new names, 111.
M‘Intosh, Prof., on the distribution
of marine animals, 117.
Macrones, new species of, 194.
Madreporaria, on the prototheca of
the, 1.
Malacostraca, on the classification of
the, 144,
Mammals, new, 71, 142, 206, 250,
323, 382, 384, 388, 405, 422.
Mantide, new, 81.
Marine animals, on the distribution
Olemliliie
Marmosa, new species of, 143.
Marthula, new species of, 248.
Maschane, new species of, 249.
Megachile, new species of, 216.
Megacelum, new species of, 196,
270.
Megalocerzea, new species of, 269.
Megalophthalmus, new species of,
98
Megalopyge, new species of, 246.
Mercennus, definition of the new
generic name, 304.
Mertila, characters of the new genus,
9
v0.
Migas paradoxus, note on, 68.
Miris, new species of, 105.
Mirperus, new species of, 352.
Mollusca, new, 452, 458; from the
Bay of Bengal and the Arabian
Sea, on, 458.
Moseleya, on the prototheca of, 1.
Mus, new species of, 416.
Mutilla, new species of, 279.
Myotis, new species of, 209, 383,
407.
Necroscia, new species of, 437.
Nemachilus, new species of, 192.
Newton, E. T., on the occurrence of
INDEX.
Hdestus in the coal-measures of
Britain, 327.
Nichomachus, characters of the new
genus, 104.
Nomia, new species of, 211, 214.
Nyctibates, characters of the new
genus, 261.
Nyctinomus, new species of, 210.
Nymannus, characters of the new
genus, 195.
Nysius, new species of, 352.
(Hnomys, definition of the new genus,
416,
Olcyphides, new species of, 445,
Ormiscodes, new species of, 245,
Orthonecroscia, definition of the new
generic name, 436,
Orthoptera, new, 81, 572, 429.
Ortmannia, on the genus, 377.
Oryzomys, new species of, 142.
Oxyartes, new species of, 574.
Pacificana, characters of the new
genus, 65.
Pamera, new species of, 267.
Paracalocoris, new species of, 110,
199.
Pelomys, new species of, 415.
Phenopharos, characters of the new
genus, 455.
Phasmide, notes on, 372, 429.
Phonolibes, new species of, 354.
Photina gracilipes, definition of the
new name, 8&6.
Phryganistriine, definition of the
new subfamily, 452.
Pierine, on African butterflies of
the subfamily, 426.
Pillay, R. S. N., on the structure of
the teeth of some poisonous snakes,
238.
Pipistrellus, new species of, 206,
387.
Placodermi, definition of the new
eroup, 340.
Plateros, new species of, 94.
Pleurotoma, new species of, 458.
Plinachtus, new species of, 351.
Pocock, R.I., on a new stridulating-
organ in scorpions, 56.
Peeciloscytus, new species of, 274.
Polyodontophis, new species of, 182.
Pomponatius, characters of the new
genus, 265.
Poulton, Prof. E. B., on the collec-
tions of William John Burchell, 45.
Promachus, new species of, 375.
Psen, new species of, 219.
479
Pseudagenia, new species of, 291.
Pseuderesia, new species of, 73.
Pseudocheeta, characters of the new
genus, 87.
Pseudophasma, new species of, 447.
Pseudoxenodon, new species of, 134.
Pseudoxiphophorus, new species of,
256.
Ptychodus, on the jaws of, 399.
Putorius, new species of, 323, 390.
Pyrgomantis, new species of, 83.
Rana, new species of, 131.
Regan, C. T., on fishes from Yunnan
Fu, 190 ; from Mexico and British
Honduras, 255; on Holocentrum
osculum and a new species of
Centropomus, 259; on a new
species of Cheetodon from the New
Hebrides, 276; on the phylogeny
of the Teleostomi, 329, 475.
Reptiles, new, 132, 450.
Rhinolophus, new species of, 386.
Rhopalurus Borellii, on the stridu-
lating-organ in, 56.
Rugosa, on the corals of the group,
114.
Russell, E. S., on Depastrum cyathi-
forme, 62.
Sabellicus, characters of the new
genus, 114.
Saccopteryx, new subspecies of, 251.
Saimiri, new subspecies of, 250.
Salius, new species of, 289.
Sanders, Miss C. B., on the lepido-
ptera collected by W. J. Burchell
in Brazil, 805, 356.
Schwann, H., on new forms of Ano- '
malurus and Sciurus, 70; on Felis
ocreata and its subspecies, 421.
Sciurus, new subspecies of, 71.
Scorpions, on a new stridulating-
organ in, 56,
Scotophilus, new subspecies of, 207.
Silurus, new species of, 192.
Smith, E. A., on mollusca from the
Bay of Bengal and the Arabian
Sea, 453.
Snakes, on the structure of the teeth
of some poisonous, 238.
Sosibia, new species of, 434.
Spatangoids, on a new genus of,
236.
Sphedanolestes, new species of, 355.
Sphendale, new species of, 86.
Steelonchodes, definition of the new
generic name, 372.
Suvalta, new species of, 220,
480
Tachysphex, new species of, 801. *
Tachytes, new species of, 296.
Tajuria, new species of, 141.
Teleostean fishes, synopsis of the
suborders and families of, 161.
Teleostomi, on the phylogeny of the,
329, 475.
Tersomia, characters of the new
genus, 431.
Theopompa, new species of, 81.
Theseus, new species of, 263.
Thomas, O., on new mammals from
S. Africa, 142; on new bats from
British East Africa, 206; on new
forms of Saimiri &ce., 250; on anew
bat from the United States, 382 ;
on new African and Asian bats,
384; on mammals from Northera
Angola, 405.
INDEX,
Thrichomys, new species of, 254,
Thysonotis, new species of, 140.
Tilapia, new species of, 155.
Tiphia, new species of, 281.
Triepeolus, new species of, 56.
Trigonophasma, characters of the
new genus, 436. 7
Tropidonotus, new species of, 152,
Trypanosoma gambiense, on the
action of arsenious acid on, 401.
Trypoxylon, new species of, 216.
Volkelius, characters of the new
genus, 271.
Woodward, Dr. A. 8., on the jaws
of Ptychodus from the chalk, 399.
Yakoyleff, Prof. N., on the corals of
the group Rugosa, 114.
Zoogoneticus, new species of, 256,
END OF THE THIRTEENTH VOLUME.
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