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ENTOMOLOGIST’S RECORD
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VOL. XXXVI."
JANUARY tro DECEMBER, 1924.
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Ua AEN
C0I008 Cf
in
the Z chromosome, and all the offspring of both sexes must be grossu-
laviata, but half the spermatozoa of the second, homozygous for sex
but heterozygous for the grossulariata-lacticolor factors, have the Z factor
in the Z chromosome. If one of these fertilises a female-producing
ege, a lacticolor female is the result, since the W chromosome
of the egg does not affect the appearance, and the Z chromosome
carries no grossulariata factor.
This has been proved by many breeding experiments, and is the
classical example of sex-linked inheritance in Lepidoptera. Another
discovery which bears on the origin of this mosaic was made by Don-
caster, who showed that in some eggs of grossulariata there are two
Fesruary 157TH, 1924.
18 THE ENTOMOLOGIST’S RECORD.
nuclei instead of one, and that each may be fertilised by a separate
spermatozoon. Although only a single insect results from such a
union, one part of it may be genetically different from the other.
One explanation of the origin of this mosaic is that, although both
parents were yrossulariata in appearance, the male was heterozygous
for the yrossulariata factor, and the female had binucleate eges
If both nuclei of one of these eggs were female producing, and one
was fertilised by a spermatozoon carrying the yrossulariata factor and
the other by one carrying the lacticolor factor, a yrossulariata-lacticolor
mosaic would be produced.
The part derived from the first union would have chromosomes
(7W in all its cells and would be female grossulariata, and the part
derived from the second union would have chromosomes ZW in its
cells and be female lacticolor. | BBE
In the ease of an ordinary egg with a single nucleus, division into
two cells takes place after fertilisation, and as a rule each of these by
innumerable subsequent divisions gives rise to half the resultant insect.
Sometimes, however, cells derived from one of these wander across and
mingle with those derived from the other. This is seen readily in
gynandromorphs, which may have streaks of male tissue amongst the
female or vice versa, although the loss of a Z chromosome, which
caused the gynandromorphism, occurred at the first division of the
fertilised ovum.
A migration of cells derived from the one fertilised nucleus amongst
those derived from the other would explain the streak of grossulariata
pattern on the lacticolor side of this specimen.
It is fortunate that this mosaic occurred in a species in which the
cytology has been so thoroughly investigated, and involved somatic
characters the inheritance of which are so well known.
All the conditions necessary for its production in the way suggested
above are known to occur in wild grossularviata. It has also been
proved that a somatic mosaic has originated from a binucleate ovum.
This example, which occurred in Drosophila is described by Morgan in
his Origin of Gynandromorphs on page 26.
A second possible explanation is that the specimen is a somatic
mutation, which originated by loss of the yrossulariata factor from the
Z chromosome, during, or immediately after t be first division of the
fertilised ovum.
In this case after the first division of the fertilised ovum was
complete, one cell would have a Z% chromosome lacking the
grossulariata factor, and would produce the lacticolor part, the other
would still have the grossulariata factor and would produce the typical
part by its subsequent divisions. Both parents in this case might have
been typical grossulariata. Since the insect is a female, with only
one Z chromosome in each cell a mutation occurring in that
chromosome would cause a visible difference in outward appearance.
The arguments for and against this origin of mosaics in Lepi-
doptera by somatic mutation were given in my former paper in the
Entomologist’s Record 1922, XXXIV., p. 105. There is no doubt that
it is the cause, which usually operates in Drosophila.
A third explanation is that the same mutation occurred in a gerin
cell of the male parent. Morgan mentions its possibility in this
A SOMATIC MOSAIC OR MUTATION IN ABRAXAS GROSSULARIATA. 19
species and points out that it would give rise to a lacticolor female,
although both parents were normal yrossulartata.
But to produce a mosaic the spermatozoon in which this mutation
occurred would have to fertilise one nucleus of a female-producing
binucleate egg and a normal spermatozoon the other.
It is obvious that the third explanation is the most improbable.
In favour of the first is the fact that we know that all the conditions
necessary for its production do exist in wild grossulariata, whereas we
do not know that somatic mutations have ever occurred in this species.
In addition there is the probability that several similar mosaics would
be found in one brood and the chance of capturing one or breeding one
from a wild larva would be much greater than in the case of a somatic
mutation, because this would only affect a single individual.
Its likelihood depends on the frequency with which Jlacticolor is
found in Aberdeenshire, and of this I have no knowledge.
The following are descriptions of two more mosaics in Abraxas
grossulariata.
(1) A female formerly in the Horne Collection. Left side
typical grossulariata, right side a lightly marked form.
(2) A female bred by Mr. H. B. Williams in June 1921, from
a wild larva found in his garden at Thornton Heath. It
is a small specimen with the wings equal on the two sides.
The upper- and undersides of both wings on the left are the usual
heavily marked London form of yrossulariata, with the fringes almost
completely black. On the right side the black markings are much
reduced, especially those on the outer side of the orange band of the
forewings, the median row of spots on the hindwing and the marginal
spots, and the fringes are white. Mr. Williams tells me he has never
met with a specimen of this lightly marked form in his garden. I
have seen specimens of both sexes marked like the light halves of these
two mosaics from Argyllshire, Durham and Bath, and elsewhere, so it
must have a wide distribution. It may be a recessive like the Q
variety, with the factor carried by an autosomal chromosome. Since
wild males are found it is not sex-linked. Each of these specimens
may have arisen from a binucleate ovum, with the nuclei differing in
the constitution of an autosomal chromosome, or with the nuclei alike
but fertilised by spermatozoa differing in the same way. On the other
hand, since both are females, they may be somatic mutations.
To my list of somatic mosaics published in this journal, 1922,
pp. 105 and 200, I add the following :—
Viminia (Acronicta) menyanthidis, Vieweg. Sex not mentioned.
Right side var. obsoleta, Tutt, left side much more strongly marked and
typical (Tutt, British Noctuae and their Varieties, Vol. 1., p. 24).
Mimas (Smerinthus) tiliae, L. Female. Right side typical with
large markings on costa and posterior margin, left side with one central
spot, var. centripuncta, Clark. The latter appears to be recessive to the
former (Bull. Ent. Soc. de France, 1895, p. xe.).
Dryas paphia. Female.
Right upperside valesina nigra (ohner schiller).
Left upperside valesina brunnea (grund schillernd).
20 THE ENTOMOLOGIST 'S RECORD,
Right underside valesina subtusaurea.
Left underside valesina subtuscoerulea.
D. paphia. Female.
Right upperside paphia rutila.
Left upperside paphia viridescens.
Right underside paphia.
Left underside paphia subtusaurea.
D. paphia. Male.
Upper surface on both sides paphia.
Right underside var. subtusaurea.
(T. Reuss, Societas Hntomologica, 1923, p. 26).
Cirrhoedia xerampelina, Hb. Right side typical, left unicolorous,
but not agreeing exactly with the description of var. unicolor, Stgr.
(Ent. Record, 1922, XXXIV., p. 18).
Mr. W. Fassnidge took it on the trunk of an ash, between Litzel-
bourg and Saverne, in Lorraine, in August, 1921. It is a female, in
which the ovipositor and both frenula were clearly seen.
Entomological Notes for the Season 1923.
By Commander GEORGE C. WOODWARD, R.N.
(Concluded from page 6.)
July 22nd, Triphaena fimbria (1), Leucania lithargyria, Leucoma
chrysorrhoea (similis), Drepana falcataria, Hypena proboscidalis, Zan-
clognatha grisealis, Hydriomena furcata.
At Wisley, on June 28rd, P. argus=aegon was still common, A.
aglaia, V. urticae, P. brassicae, P. gamma. A. myrtilli, appeared to be
over, as I did not see one.
On July 30th I spent a couple of hours at Box Hill, and the fol-
lowing species were noted :—Avgiades sylvanus, Zygaena filipendulae,
very abundant everywhere, Hpinephele jurtina and C. pamphilus, also
abundant, P. rapae, O. bipunctaria and A. aylaia.
The evening at Oxshott, on July 31st, produced Hepialus sylvina,
which I found rather difficult to capture, A. secalis and ab. leucostigma,
Noctua baja, Triphaena pronuba, Finnomos elinguaria, Leucania impura
common, and Petilampa arewosa common. I found P. brassicae quite
commonly asleep on the bushes, a most conspicuous object in the rays
of the lantern.
On August Ist I again tried Shoreham, in Kent. Polyommatus
(Agriades) coridon was most abundant in a grass field close to the
station. A. aylaia was also quite common, but seemed to be
getting worn. In the same field I noticed P. rapae, P. napi, P.
brassicae, Coenonympha pamphilus, H.jurtina, A. sylvanus, Z. filipendulae,
O. limitata and O. bipunctaria.
At Oxshott, on August 2nd, I found a small sallow bush covered
with the secretions of aphids, it simply swarmed with Noctuae, mostly
common, for about a couple of nights. The following were in abund-
ance:—T’. pronuba, N. baja, I.. impura, Caradrina morpheus, H. nicti-
tans, A. ab. leucostigma, and also 7’. comes=orbona, T. janthina, T. inter-
jecta, M. maura, A. secalis and X. monoglypha not common.
On August 8th I again went to Bramshott. I found Vanessa io
GEOGRAPHICAL VARIATION IN HIPPARCHIA SEMELE, L. 21
swarming on thistles, witha few G. rhamni g ¢ and 2 2, P. brassicae,
A. urticae, D. paphia, which was very worn; I only saw two specimens
of Hipparchia semele, when last year it was abundant; also a few P.
icarus. Up to now P. ticarus has been conspicuous by its absence, I
have seen only about four specimens of it this season.
I paid another visit to Oxshott on the evening of August 28th. I
found X. fulvayo common, just emerged. This moth seems to like
sitting on tall grass stems in the vicinity of sallow bushes, and is a
most conspicuous insect in the rays of the light.
During the first fortnight in September I was again in Shropshire,
and have never seen J’. to in such abundance as I did between the
6th and 10th, every field that had scabious growing in it simply
swarmed with this insect. Polygonia c-album was found more
frequent than usual; this species seems to like scabious growing just
outside a wood, and the individuals seem to stick to the same spot day
after day. I also noticed a few Pyramets cardui, P. atalanta and
Aglais urticae. P. icarus was common, the first time I have found it
commonly this year.
I spent an hour or two pupa digging, getting a few dozen pupae,
the only ones to emerge so far being Hadena protea and Cidaria miata,
which appeared on the 16th of September.
This practically ended the season as far as I was concerned.
Geographical Variation in Hipparchia semele, L.
By ROGER VERITY, M.D.
(Concluded from page 156.)
Let us now examine the races which constitute the various grades
of lines A and H, classifying them according to the average intensity .
and extent of the network on the underside of the hindwing. One
finds these two lines divide in corresponding grades, and that roughly
the corresponding ones often are found in about the same regions, and
follow each other from north to south, so that a very natural and con-
venient classification is obtained. ‘I'he same order is suggested by the
tone of the suffusion, which turns, as already stated, from dark grey to
light grey and then to tawny, according to the general rule in Lepi-
doptera that dry heat turns black into tawny. This of course is much
more conspicuous in line EK than in A, because in the latter the suffu-
sion is limited in extent.
Grade I.: Line A is represented in this grade by race scota, Vrty.,
Bull. Soc. Ent. France, 1911, p. 313, pl. I., fig. 10, one of the most
distinct of the species; it is the smallest in size: the fulvous is so
extensive, it is only surpassed by aristaews and equalled by siciliana,
but it is of an extremely dull, pale yellowish tone: the network of the
underside is very thick and very deep black in tone and uniformly
spread all over the wing, so that the narrow, white, band-like space
only just shows through it vaguely ; the black streak, which usually
marks its inner outline in all the other races is obliterated here. My
“types”? are from the northern coast of Scotland. It is remarkable
that the greatest amount of fulvous exhibited by the species should
thus be produced in the extreme north and in the extreme south of
Hurope (Corsica, Sardinia, and Sicily). The English race is larger
than scota, but always smaller than the continental ones, and, in other
29, THE ENTOMOLOGIST’S RECORD.
characters too, it answers the designations either of race scota trans.
ad jubaris and ad semele or of jubaris and.of semele trans. ad scota,
coming nearer one or the other of these races, according to latitude
and localities.
Tutt, in his Handbook of Brit. Bntts., p. 898 (1896), points out the
the difference of upperside between the male of line A and that of line
HK, and names suffusa the extreme individual form of the latter, deserib-
ing it as ‘almost unicolorous without pale bands.’ This name should,
I think, be used as Tutt meant it to be, for the particularly melanic
individuals of any race they may occurin. One must make a very
clear distinction between this sort of name and those waich apply to
an entire race or generation, taken on the whole, and which stand, as
rule, for a combination of various characters. These must all be taken
into account when the name is used. It was very misleading of Tutt
to apply the name of aristaeus, Bon., to British females ‘‘ with rich
fulvous transverse bands.” As to the two English races of lines A and
Hi, I have hesitated as to whether they should be named or not. The
fact they. are so much collected and handled and that they represent
entities of particular interest to the numerous British entomologists
has, however, pushed me to suggest a less cumbersome way of desig-
nating them than the “trans. ad’? form. I thus propose the names of
angliae, mihi, for the race describable, in size and pattern, as inter-
mediate between scota and jubaris, and of anglorum, mihi, for that of
line H, smaller than nymotypical semele and with an average darker
underside.
Line E is found in grade I. in race cadmus, Fruhstorfer, /nt.
Ent. Zeit. Guben, April, 1908, p. 10, described from Klausen in South
Tyrol, and recorded in the original description also from the Valais,
the Simplon route, Zermatt, and Geneva. I possess it from Oropa in
Piedmont, from Moravia (transitional to semele), from Mt. Sumbra, m.
1,200, in the Apuane Alps (N. W. of Tuscany), and from Saint Come
Bazas (S.-W. of France), so that its range is very extensive in the
southern part of Central Europe. The characteristics of line H,
described above, are exhibited by this race to their highest degree
(fulvous very limited and very warm in tone on upperside; very reddish
also on underside of forewing; underside of hindwing dark suffusion,
very black and extensive, greatly restricting and often nearly abolish-
ing the white band-like space, which, anyhow, is always covered over
by the thick black network of streaks). All these characters are evi-
dently the result of warm, damp surroundings.
Grade II. consists of the races found in the northern part of
Central Europe. ‘They are very variable, individually and locally, and
they are only surpassed in this respect by aristaeus. In size they
range from that of the Hnelish races to the larger size of more
southern ones, and the average is about intermediate. In pattern and
colour they culminate in two widely different forms, very characteristic
of line A and of E respectively. The former has been called jubaris
by Friihstorfer (/.c.) from “ types’’ of Hastern Prussia, described as
having ‘‘very prominent bands of a light ochre yellow on all the
wines.” It should be added that in this form the underside of the
hindwings is very light in general tone; network thin ; quite absent
GEOGRAPHICAL VARIA'TION IN HIPPARCHIA SEMELE, L. 23
on the broad, white, band-like space, which is left uncovered by the
very limited suffusion ; the latter is also of a very light gray or tawny.
The specimens I have from the northern coast of France (Paris-Plage,
in the Pas-de-Calais) are the most characteristic | have seen. The
form of line E, which belongs to grade II., is that which I take to be
the nymotypical one of semele, although I cannot affirm that this is its
proper name, because I am not acquainted with the Swedish race.
This last is certainly nymotypical, Linneus’s first quotation being his
own description in Fauna Svecica. By naming jubaris, Frihstorfer
has restricted the Linnean name to the darker form, with no fulvous
on the forewing of the male (or only two or three small spots), with
this colour more limited generally in both sexes, and of a warmer tone,
and with a much darker underside to hindwings; the network is
thicker and more extensive, although less so than in scota; the suffu-
sion is blackish ; in the male they both leave, as a rule, a complete,
and sharply outlined band-like space of a pure white, which stands out
boldly on the darkened remaining parts of the wing; in the female
this space is entirely obliterated or vaguely visible through the net-
work. I possess this race from the Pont-de-l’Arche (Kure) and from
Les Boutardiéres (Maine-et-Loire). It evidently is found in some
localities and jubarts in others of the same regions. There remains to
establish definitively whether it is found in Sweden, and whether it
thus really is nymotypical semele.
Grade III. is exhibited, in line A, by race teres, Frubstorfer (l.c.),
described from Digne in the Basses Alpes, which takes the place of
jubaris in the south of Kurope. It is on the whole larger than the
latter, of a slightly warmer tone of fulvous, and distinctly a grade
lighter on the underside; the white ground colour has often a slightly
golden hue and it is broadly uncovered, forming a very wide band,
because the dark suffusion is very limited and of a very pale trans-
parent gray, or yellowish-gray ; the net-work is very thin and in some
individuals obliterated on extensive areas; in others it spreads all over
the wing, but the white band is not much obscured by it, owing to the
extreme slenderness of the little streaks. Near Florence the race is
found on Mt. Conca, m. 400, on the northern slopes of Mt. Morello,
whereas, only a few miles away, on the blazingly hot and parched Mt.
Fanna, 600 m., one finds the race I am about to describe.
Grade ILI. of line E is the race which replaces cadmus in peninsular
Italy ; the fulvous of the upperside is perhaps a little less saturated,
and more vivid, but otherwise that surface resembles it exactly in the
male sex by the total, or nearly totai, absence of fuivous on the fore-
wing and by the small triangular patches of the hindwing; the fore-
wing of the female exhibits broad spots, clean-cut in outline and of a
clear, brilliant fulvous, which stand out boldly, and confer a strikingly
finer appearance to this race than to the other continental races. The
underside of hindwings is distinctly different from cadmus, because the
general tone is much lighter; this is due to the fact that the network
is thinner and the suffusion is of a very pale gray (it will be observed
that this is the very character which distinguishes the race of Pararge
meyera, li, of this region, from those found further north and west) ;
the central white band-like space is never entirely abolished in the male,
as 1s often the case in the darkest cadmas individuals, but it is always
narrow, irregular in outline, and usually most of it is veiled over by the
24 THE ENTOMOLOGIST’S RECORD.
thin network, so that it does not stand out, as it does on the darker
wing of nymotypical semele. Individual variation, however, is con-
siderable, because the darkest individuals point to cadimus, whereas the
lighter ones approach teres in some cases, and recall distantly the
uniform gray of mersina in others; the first mentioned are met with
chiefly in Tuscany ; apart from these, I detect no differences between
my series of Tuscany and those collected in the Aspromonte, at 1,200
m., in southern Calabria. I name it paeninsulitaliae. “Types,” from
Mt. Fanna, 600 m., near Florence.
Grade IV. in line A is the culminating degree of reduction of the
network of the underside, because in this line it is never entirely
abolished, as it can bein B, C, and E. It is exhibited by race siciliana,
Obth., Ht. Lép. Comp., X., p. 180, fig. 2815-6 (March, 1915), described
from specimens “collected in Sicily by Bellier.” I possess several
collected by Ragusa at the Ficuzza and other localities. It is the
largest race of the species, and one of the most striking. On the upper-
side the fulvous is only surpassed in extent by aristaeus, but it is not
as bright and reddish as in the latter; in both sexes there is a very
broad band across all the wings, but its inner outline is sharply defined
and never shades off towards the base as in that race; in the female
there is always a diffused patch in the middle of the forewing, usually
more extensive than in algirica, but never blending completely with the
band, as in aristaeus. On the underside of the hindwings the dark
suffusion is very pale and limited, so that a very broad central strip
and a basal patch of the white ground colour are left uncovered. It is
interesting to remark that the features of this Sicilian race and those
of aristaeus exactly correspond to those of Pararge megera, L., from the
same regions: in both cases the greatest extent of fulvous produced by
the species is found in Corsica aud Sardinia, but the Sicilian race only
just falls short of reaching it; in both cases it is combined with a very
dark underside in the former region, and with the lightest produced by
the species in the latter region. The parallelism is carried on also in
Greece by the dark upperside combined with a light underside (in
senthes, as in lyssa), and in the transitional race of Peninsular Italy (in
paeninsulitaliae, as in praeaustralis and in paeninsulitaliac). One won-
ders how local causes can produce such resemblances in all these '
regions in two species so little like each other! It shows to what an
extent surroundings influence some variations, whereas others are evi-
dently, to a considerable degree, produced independently of this
influence, the characters of line A and those of line EK occuring in
the same regions, and even on the same grounds, as individual varia-
tions. In Sicily the differences between the races of these two lines
A and E are more accentuated than in any other region :—
Grade IV. of line E consists, there, in a race | have from the Caronie
Mts., at high altitudes, which contrasts very markedly with siciliana by its
smaller size, very limited extent of fulvous above (none on forewing of
male), which is also more saturated and reddish in tone, and by the
remarkably dark underside of the hindwings, with a narrow, but very
clear white and sharply outlined band-like space standing out on them.
At first sight all this seems quite asin nymotypical semele of the north;
further observation shows instead that in the Sicilian race the black
network is as limited in extent as in siciliana, but that it is replaced
here by the dark suffusion, which is usually black, and very extensive,
GEOGRAPHICAL VARIATION IN HIPPARCHIA SEMELE, L. 25
absorbing what little network there is. ‘This race seems to be the one
Friihstorfer has described by a few vague words, from the female alone,
in the Hntom. Zeitschr., 1908, p. 98, under the name of blachiert. In
1914 I made the mistake of describing in the Bull. Soc. Ent. Italiana,
XLYV., p. 219, the male of siciliana, Obth., as that of blachiert, but, now
I am acquainted with the two Sicilian races, I can see that the darker
one is that named by Fruthstorfer. Both these authors are wrong in
stating their race is a near ally of alytrica. Stauder, too (Zeit. wissen.
Insektenbiol., 1916, p. 59), is not correct when he refers his semele of
Sorrento and of Calabria to blachieri or a transition to it; they, of
course, are paeninsulitaliae and thus, if anything, they point dis-
tantly to mersina, and on the underside rather to siciliana, on account
of the light gray tinge of the suffusion.
As grade V. of line E I consider race mersina, Stdgr., Cat. Lep. Pal.
II. ed., p. 28 (1871), described from Mersina in Cilicia, and found in
the north of Asia Minor generally and in Syria, either in well charae-
terised forms or in others transitional to the races of Greece. In the
former case the upperside has very limited fulvous spots in the male
and those of the female resemble paeninsulitaliae. The characteristic
of this race, however, consists in the absence of network and in the
nearly uniform gray, or brownish-gray suffusion on the underside of the
hindwings of the male, which thus stands well as the culminating
degree of line EK. Race maderensis, Baker, of Madeira, described as
extremely dark on both surfaces, I cannot place, because I am not
acquainted with it. I can only say the same of diffusa, Butler, from
Asia, also described as very dark.
The relationship of the different lines of variation just described is
an interesting subject, but it can only be developed well by dealing
more generally with the variations of other genera. The following
table may be found useful as a summary and as a help to one’s memory,
but I cannot claim it to be a true representation of the positions the
lines occupy as compared with each other, because they cannot-be shown
on a single plane. If one places on the plane of the page the lines I
have called A and HK, because they consist in the two groups of races,
whose features differ more widely from each other, the other lines
should not stan: between them, but on other planes. The space
between A and E is filled up by the numerous individual forms of
transition one meets with continually in nature, and which do not in
the least pass through B and C. Line D, if anything, is a combination
of upperside and underside characters, which is actually found amongst
them. Line B of aristaeus, by the extent of fulvous on the upperside,
should stand before A, but the underside of many individuals swings
the balance so far towards H,, that one feels obliged to place it between
these lines, and the resemblance of some females to some of algirica,
also suggests that these two lines, B and C, should be kept close to each
other. Line C certainly stands quite apart on account of the shape of
the fulvous spots on the forewing of the male above; their similarity
to those of the female and consequent lesser sexual dimorphism
suggests that the more extensive and continuous band of the male in
line A and the tendency, on the contrary, to obliteration of the fulvous
in line E, might be two divergent variations, which have sprung from
it. That is why I have placed algirica in a central position. Its
underside, however, brings it markedly nearer to line EK than to A.
26 THU ENLOMOLOGISY’S RECORD.
Nain B C D E
ey ascota uibs cadmus
Il. : jubaris gee i semele
; I] é pate
IIl.: teres aristaeus eee pati paeninsulitaliae
apenninigena }
Vita stort vam ates hibera blachiert
Vine ae ete \ merstna
algirica — )
The Roman figures indicate decreasing grades in the extent and
thickness of the black network on the underside of the hindwings. In
column B the dots are meant to show that individual variation is so
unusually broad as to cover all the grades in single race. It must be
borne in mind that individual variation does in most races embrace
more than one grade, but to a much lesser extent than in aristacus.
In A line of variation the fulvous of the upperside is extensive, and its
tone is not saturated, although it does become slightly warmer and
brighter from I. to LV. ; on the forewing of the male it forms a broad
continuous band; on the underside of the hindwings the dark suffusion
is limited and pale, as compared with the other lines, and it becomes
increasingly so from I. to IV.
In B the fulvous of the upperside is more extensive than in any
other line, and it spreads to the base of the wings; its tone is very warm
and bright; on the underside of the hindwings the dark suffusion is
always very extensive, whatever extent the network has.
In C the fulvous of the upperside is intermediate in extent between
A and E,; on the forewing of the male it is divided, in grade Y., into
spots, as in female ; its tone varies as in A; suffusion of the underside
very extensive, and particularly so in grade V., but tawny rather than
black.
In D the fulvous of the upperside is as limited as in EH, but as cold
in tinge as in A; the underside suffusion is limited and pale, as in the
corresponding grade of line A.
In E the fulvous of the upperside is very limited in extent, especi-
ally in the male sex, in which it is more or less entirely obliterated on
the forewing; it is of a very saturated, warm tinge, and often very
bright; the underside suffusion is dark and usually very extensive, but
more particularly so in grade V.; from I. to V. it turns on broad lines
from dark gray to light gray, and then to tawny, except in blachiera,
where it is quite as black as in cadmus.
I OTHES ON COLLECTING, etc.
BoarMia ABIETARIA AT GRAVESEND.—In August, 1922, I captured
two B. abietaria, a male in fair condition on August 14th, beaten from
a yew, and a female on August 17th in perfect condition on the trunk
of a beech tree close to the same yew tree, when sugaring.
This insect 1s new to this district. Is it new to Kent?—F. T.
Grant, 87, Old Road West, Gravesend.
AN EARLY APPEARANCE OF HuprrHecra PuMILATA.—On January 25th,
I saw an apparently recently emerged example of #. pumilata resting
on the wall of my sitting-room. Our authorities tell us that it can be
NOTES ON COLLECTING. 27
found from April to November, but January is certainly an unusual
month for the species.—Hy.J.T.
New sprcies to Great Brirain.—We have recently seen no less
than six species of Micro-lepidoptera already this year which our best
authorities have been unable to identify with any hitherto known
British species. Even in the best well-worked orders no doubt
novelties will still reward the persistent workers.—Hy.J.T.
BRENTHIS EUPHROSYNE, Li. ap. PLUMBKA, CockAyNE.—I owe an
apology both to Dr. Cockayne and to readers of the Ent. Record. for a
slight error in the note on this form on p. 8 of this volume. My
specimens were taken, one in 1916 (which is now in Dr. Cockayne’s
collection), the other (the type, which is in my own collection) on May
27th, 1922. In communicating the facts verbally to Dr. Cockayne I
doubtless failed to make these dates clear—H. B. Wuixuiams, Briar
Cottage, Claygate, Surrey.
LapyBIRDS HIBERNATING IN THE HousE.—I have also experienced
this phenomenon in a somewhat spectacular form this autumn.
During September, 1923 (I have not noted the exact date), the species
referred to in the note on p. 9 of this volume, entered my house in
great numbers. In almost every room in the house there were
hundreds on the walls and ceilings, mostly in small groups of a dozen
to twenty. Many hundreds were swept up and ejected, but they are
still present in crevices, etc. Recently the removal of a hollowcurtain rod
revealed the presence of a great number, in fact my wife tells me it.
was almost full.—In.
Dasycuira FasceLina IN Surrey.—In May, 1921, 1 found upwards
of sixty of the larvae of this species sitting on the top sprigs of
heather on Hankley Common, near Elstead, Godalming. They were
apparently confined to quite a small area. The pupae were chiefly
found in pairs, and the silken pads, on which they change their skins,
made the task of finding them considerably easier. Exceptionally
small moths emerged and a very large number died in the pupa stage.
Despite repeated attempts I have been unable to find the species since
1921.—H. B. D. Kerriewett, Pageites, Charterhouse, Godalming.
PHILOPHORA PLUMIGERA IN Surrey.—On November 12th, 1928, a
friend of mine noticed what he took to be a dead moth in an electric-
light in the road at Godalming. On closer examination it was found
that it was a specimen of P. plumigera and not quite dead. On
November 18th I took two other 2s at the electric-light, one at rest
on the standard and the other flying round the lamp. The Charter-
house Records for the District show that two males were taken in 1888
and this points to the fact that this species is well established here.—
Ib.
Nota conrusa 1x Hypr Parx.—lI took one specimen, newly-hatched,
of the ‘‘ Least Black Arches” on April 14th, 1923, sitting head-
upmost on a poplar tree. Both the dates and the localities seem
unusual.__Ip. [Flies in May-June.—H.J.T.]
28 THE ENTOMOLOGIST S RECORD.
SHSIA ANDRENAEFORMIS.—Few people seem to be aware that this
Clearwing, generally considered a rarity, is. particularly common in
certain localities along the Hog’s Back, especially the Guildford end.
The “ Wayfaring Trees’ there are riddled with the larvae to such an
extent that whole limbs of bushes die down because the interior is
eaten out. By cutting the stems in late May, wherever the well-known
round hole is to be seen, as many specimens can be collected in a single
day as will ever be needed for the collection. The time of the
emergence varies with the season; only about half of the collected
twigs produce the required results as the life-cycle lasts two years and
a good proportion of the larvae may be in their first year only.—Ib.
Catymia TRapEZINA.—Mr. G. B. C. Leman sent me a specimen of
this moth which he had taken, while beating for Coccinellidae, on an
oak in a friend’s garden. His capture rather approaches ab. nigra in
form. ‘The species is not rare, but the locality (Putney) seems to me
most unusual. It was taken in July, 1923.—Ib.
G{URRENT NOTES AND SHORT NOTICES.
The Annual ‘“ Verrall Supper” took place on January 15th, as
usual on the day before the Annual Meeting of the Entomological
Society of London, and was a most successful gathering; no doubt
the improved weather was no small factor in the large attendance,
for more than 180 were present out of the 140 acceptances:
Among those present were, B. W. Adkin, J: H. Adkin, R. Adkin,
H. W. Andrews, KE. B. Ashby, S. R. Ashby, J. B. Ashworth,
EK. C. Bedwell, G. Bethell, G. T. Bethune-Baker, K. G. Blair,
S. Blenkarn, Col. W. Bowater, L. A. Box, H. Britten, R. T. Bowman,
F. B. Carr, Prof. J. W. Carr, G. C. Champion, C. A. Cheetham, Dr.
HK. A. Cockayne, J. HE. Collin, Joseph Collins, B. H. Crabtree, Capt.
Crocker, Dr. J. Davidson, L. K. Dunster, J. H. Durrant, H. Donisthorpe,
_H.M. Hdelsten, F. W. Edwards, Stanley Edwards, HK. Willoughby-
Kllis, Dr. H. Eltringham, E. Wylie Fenton, Dr. Fremlin, L. T. Ford,
G. F. W. Fox- Wilson, G. E. Frisby, F. W. Frohawk, J. C. F. Fryer,
Dr. C. J. Gahan, F. Gilhatt, C. T. Gimmingham, EK. EK. Green,
A. de B. Goodman, O. R. Goodman, T. H. L. Grosvenor, A. T. J.
Gedye, H. M. Hallett, A. H. Hamm, B. 8. Harwood, P. Harwood,
H. C. Hayward, Capt. A. F. Hemming, T. F. P. Hoar, H. Hodge, Dr.
D. Hunter, H. C. Hugeins, G. L. R. Hancock, Prof. 5S. Image, Dr.
A. D. Imms, O. E. Janson, C. F. Johnson, D. C. Johnstone, Dr. K.
Jordan, W. J. Kaye, F. A. Labouchere, L. Lacey, F. Laing, H. A.
Leeds, G. C. Leman, Prof. J. J. Lister, R. W. Lloyd, T. A. Lofthouse,
W. J. Lucas, G. T. Lyle, A. H. Macmurdo, H. Main, W. Mansbridge,
H. H. May, A. W. Mera, Dr. Chalmers Mitchell, J. P. Mutch, L. Nell,
W.G. F. Nelson, L. W. Newman, C. Nicholson, F. A. Oldaker, J. Peed,
F..N. Pierce, Prof. KE. B. Poulton, R. M. Prideaux, W. Rait-Smith,
Col. Rattray, Capt. N. D. Riley, A. H. Ruston, A. Rymer-Roberts,
Lord Rothschild, P. F. Skinner, L. G. Saunders, J. W. Saunt, Dr.
R. F. Scharff, W. Schmassmann, Hugh Scott, Lieut. Seabrook, V. EH.
Shaw, W.G. Sheldon, C. E. Stott, R. Stenten, H. Step, HK. EK. Syms,
G. Talbot, W. H. Tams, Rev. J. E. Tarbat, M. L. Thompson, Rev.
A. Thornley, A. EK. Tonge, H. J. Turner, C. J. Wainwright,
SOCIETIES. 29
Commander J. J. Walker, S. Walker, J. D. Ward, G. EK. R. Waters,
J. H. Watson, B. S. Williams, EH. J. Winstanley, L. Bonaparte- Wyse,
and H. B. Wilhams.
The Annual Reports of the London Societies seem to be of a most
excellent nature. Both the Entomological Society of London and the
South London Entomological Society have higher membership than
ever before in their history. The former has in the past three years
paid off more than three-fifths of the debentures issued to purchase
their freehold premises at 41, Queen’s Gate, and the latter have suc-
cessfully found funds to pay for the extremely good proceedings
recently issued. The Treasurers of the Societies are to be heartily
congratulated for their persistent intensive work on behalf of their
respective society.
SOCIETIES.
Tue Sours Lonpon EnromoLocicaL Society.
November 22nd.—Annuau Exuierrron.—Messrs. O. R. and A. de B.
Goodman exhibited butterflies taken by them this year on the conti-
nent: in the Riviera (spring), Zerynthia polywena var. cassandra,
Euchloé crameri and var. ausonia, ete.: in the Basses Alpes, Melitaea par-
thenie, Argynnis niobe ab. orientalis, bleached Hpinephete jurtina var. his-
pulla, ete.; at Digne, Leptosia duponcheli, Hesperia sidue, Thestor ballus,
ete.: near L. Maggiore (summer), A. cydippe ab. cleodowa, Neptis lucilla,
Dryas paphia ab. valesina, ete.; at Reazzino, Heteropterus morpheus, ete.;
and at Pontresina and in the Hngadine, Parnassius delius, Drenthis
thore, Melitaea varia, Krebia alecto, Colias palaeno, Plebeins donzelit,
ete.; and a worn Syntarucus telicanus from the Val de Fain.
Mr. A. E. Stafford, series of aberrations of Polyommatus (Agriades)
coridon from Royston.
Mr. Worsley Wood, three hybrids of Xanthia (Mellinia) ocellaris and
X. (Citria) fulvago bred in 1922; and gave notes on the brood and on
his other attempts to hybridise these species.
Mr. J. J. Fisher, series of Lycaenids illustrating striate forms of
aberration and variants of 7’. ballus, T. polyxena and a melanic Melitaea
dictynna.
Mr. Leeds, a very large number of aberrations of British butterflies
taken this season largely in Herts and Hants, worked out and named
on the basis of the nomenclature in Tutt’s british Lepidoptera, vols.
I.-IV., and Courvoisier’s Die Schmett. Schw., Polyommatus (A.) coridon
was especially dealt with.
Mr. R. Adkin, representative series of Diacrisia mendica, two broods
of a second generation of race mistwa, and gave notes on the breeding.
Also a Pyrameis atalanta with the large white blotch much obscured
by black.
Mr. Holford, a remarkable and unique aberration of Triphaena pro-
nuba with black-brown suffusion and suppression of the bright orange.
Mr. R. T. Bowman, a striate Abravas grossulariata.
Mr. Greer, of Tyrone, aberrations of Pieris napi, light, dark, extra
spots, pale yellow, Huchloé cardamines, abs. schepdaeli, ab. caulosticta,
? streaked with orange, ete., Melitaea awrinia, extra spotted P. megera,
several ab. addenda of EH. jurtina and one near var. hispulla, spotted
Coenonympha pamphilus, a number of ab. icarinus of P. icarus with a
streaked @ , etc.
30 THE KNTOMOLOGISL’S RECORD.
Mr. D. Pearson, FH. jurtina, bleached and ab. addenda, gynandro-
morph of P. (4.) coridon, dark M. aurinia and an obsolete underside, a
black Limenitis sibilla, E. cardamines 2 with orange ‘patches, streaked
and obsolete /’. (A.) thetis, a white R. phlaeas, etc., and from the
Simplon area Plebeius sephyrns race lycidas, Hrebia christi, M. dictynna
forms, EH. pronoé var. pitho, L. arion var. obscura with British L. arion
for comparison, etc. i
Capt. Crocker for Mr. Sperring, variable series of bred P. aegeria,
black suffused Brenthis euphrosyne, with P. aegon (aryus) showing range
from leaden to violet-blue.
Mr. C. H. Williams, aberrant series of R. phlaeas and P. (A.) coridon.
Mr. Tonge, series of P. (A.) coridon aberrations, including a fine
striated ¢, and ab. cinnus, unusually common this season, series of P.
(d.) thetis, including an obsoleta and blue suffused Qs, spotted C. pam-
philus, an extreme aberrant and suffused Cleora jubata (glabraria), and
two ab. g polonus of P. (A.) thetis, ete.
Mr. A. A. W. Buckstone, a series of the recently differentiated
Anaitis efformata, and pointed out the facts of its differentiation.
On behalf of Mr. and Mrs. Castle-Russell, aberrations of British
Lepidoptera 1922-3, melanic ?s of D. paphia, LE. jurtina g resembling
?, a striated B. evphrosyne, series of abs. of B. selene and M. aurinia, a
pale yellow P. (A.) coridon, and forms striate and obsolete, etc.
Mr. A. W. Vernon, Rhopalocera from the Austrian Tyrol B. thore,
E. lappona, E. pronoé var. pitho, M. aurinia var. merope, etc.
Mr. A. W. Mera, species that have developed, in recent years, a
marked tendency to melanism, Hpirrita (Oporabia) christyi, HK. (O.)
autumnaria, L. multistrigaria, and Hybernia defoliaria.
Capt. Hemming, striate aberrations of British Lycaenids showing
two forms assumed, internal and external, according to their origin
and direction.
Mr. L. W. Newman, an Arctia caja, brown forewings with zigzag
markings near apex.
Mr. H. Candler, eggs of the Blackheaded Gull from Scoulton Mere,
showing remarkable extremes of coloration.
Mr. Garrett, a fine ab. schmidtii of R. phlaeas from Bexley.
Mr. Grosvenor, the wonderful ab. of Z. filipendulae taken by him
at Royston, with a duplicated forewing in place of a right hindwing,
with other Zygaenid aberrations.
EVIEWS AND NOTICES OF BOOKS.
‘‘Socran Lire Amone tHE InsEcts”; being a series of Lectures
delivered at the Lowell Institute in Boston, in March, 1922, by
William Morton Wheeler, Ph.D., Sce.D., Harcourt, Brace and Co., New
York. Pp. i.-vii.+ 3875, with 116 text figures. 1923.
This splendid volume is undoubtedly a work of the first importance;
extremely interesting; most carefully thought out ; and a most valu-
able contribution to the science of both Entomology and Natural
History in general.
It is well known to most people that ants, bees, and wasps, and
also termites, live in social communities; but not that such phenomena
occur also with other insects. Here, however, they will learn, not
only that such is the case, but will also obtain a good idea of the
origin and development of such a mode of life.
REVIEWS AND NOTICES OF BOOKS. 31
Anyone who carefully reads this book is obliged to take a much
larger and broader view of social life among insects, and to regard the
subject as a whole from quite a new standpoint.
Let us now proceed to examine the contents of this attractive book.
In the preface the author points out that he has endeavoured to throw
emphasis on the fundamental nutritive motifs in the phylogeny, onto-
geny, and maintenance of insect societies, and he gives generous
thanks to all those to whom he is indebted for the loan of photographs
and drawings for some of the beautiful illustrations with which the
book is freely embellished. The work is then divided into six lectures;
a Documentary Appendix; an Index of Subjects; and an Index of
Authors.
Lecture I. ‘General Remarks on Inseet Societies. The Social
Beetles.’ The first nimeteen pages are devoted to the General Remarks
and space will only allow us to deal with them very briefly. We are
not entirely in agreement with all the views expressed by Prof. Wheeler,
as we are considerably more of a Darwinian than he is, and also we do
not much believe in “the greater mutual helpfulness,” or ‘ the draw-
ing together of nations,” etc.; but as these are purely matters of
personal opinion, and have nothing to do with facts, we will leave it at
that.
The immense age of insects—some 300 million years !—is com-
mented on; and the author finds that social habits have arisen no less
than 24 different times, in as many different groups of solitary insects.
A list of the groups that form these various societies is given in the
accompanying table.
Scarabaeidae (Copris, Minotaurus).
Passalidae (Passalus).
Tenebrionidae (Phrenapates).
Silvanidae (Vachiyalia Beetles).
Ipidae (Ambrosia Beetles).
Platypodidae (Ambrosia Beetles).
Sphecoidea.
Sphecidae (Sphea).
. Bembicidae (Digger Wasps).
CoLEoPTERA.
(Gynandrarchic). |
|
D> OVE oy BO
@ 3
Vespotdea.
9. Kumeninae (Synayris).
0. Zethinae (Zethus).
. Stenogastrinae (Stenogaster).
3 oi Epiponinae (Chartergus, Belonogaster,
etc.).
*13. Rhopalidiinae (fhopalidia, etc.).
*14. Polistinae (Pulistes).
*15. Vespinae (Vespa),
Apidae.
16. Halictinae (Halictus).
17. Ceratininae (Adlodape).
*18. Bombinae (Bumble-bees).
*19. Meliponinae (Stingless Bees).
*20. Apinae (Honey Bees).
*21. Formicidae (Ants).
HYMENOPTERA.
(Gynarchic).
32 THE ENTOMOLOGISL S RECORD.
DERMAPTERA. 22. Forficulidae (Harwigs).
(Gynarchic).
Empiparia. — - { 23. Embiidae (Hmbia).
(Gynarchic). (
TsoprEra. ( “24. Termitidae (Termites, or ‘‘ White
(Gynandrarchic). — | Ants”’.
In this list those marked with an asterisk are definitely social, the
rest being incipiently social or subsocial. In the Termites and all the
beetle groups the colony consists of a male and female parents and
their offspring of both sexes; in all the Hymenoptera, Dermaptera, and
Embidaria, the female alone founds the colony, which is developed by
her daughters. The former groups are, therefore, gynandrarchic,
the latter gynarchie.
The rest of the lecture is devoted to the six beetle societies which
have been developed by species belonging to as many different natural
families.
Space will only allow us to touch on a few points of interest; but
where all is so interesting 1t is difficult to know what to mention and
what to leave out. It may be stated here that throughout the book
the author gives full credit to all other observers for their work on the
life-histories and habits of the insects mentioned.
The life-histories of the Sacred Scarabaeus and other dung-rolling
beetles are thoroughly explained, and the illustrations show them
trundling their pellets and fashioning the dung in their subterranean
chambers. The stridulating of the larvae of Paussalus sps. is described
and figured, and their colonies are shown to consist of a male and
female and their progeny. In the “ Tachigalia Beetles,’ Wheeler
recapitulates his most interesting discovery, made in the jungles of
British Guiana in 1920, of a couple of Silvanid beetles, which occur
in the hollow leat-petioles of young trees of a Vachigalia (T. paniculata).
Both the adult beetles, and their larvae in all stages, have learned to
stroke certain mealy-bugs, which find their way into the leaf-petioles,
with their antennae as ants do, and feed on their excreta.
The author summarises the main points of interest in connection
with the social beetles. To briefly mention a few of them :—
The six unrelated families are all very ancient; the substances on
which they feed are remarkably diverse ; the father beetle co-operates
to a greater or less extent with the mother beetle in providing for the
young. :
Lecture II. ‘* Wasps Solitary and Social.’’—This is an extremely
interesting chapter, and one feels that any extracts one can give, or
any remarks one may make in the space of a review, can but feebly
represent the beauty.of this lecture. It must be read as a whole to be
really appreciated as it deserves, As the lecturer truly observes, wasps
bave attracted fewer investigators than the ants and bees, though they
are of even greater interest to the student who is tracing the evolution
of specialised instincts and social habits. He divides the enormous
Wasp group into two great complexes, the Sphecoids and the Vespoids,
and he establishes some seven generalisations of which the following
are the chief points :—
(To be concluded.)
Subscriptions for Vol. XXXVI. (10 shillings) should be sent to
Mr. Herbert E. Page, ‘‘ Bertrose,’’ Gellatly Road, New Gross,
S.E.14 [This subscription includes al! numbers published from
January 15th to December 15th, 1924.)
Non-receipt or errors in the sending of Subscribers’ magazines should be
notified to Mr. Herbert EH. Page, ‘‘ Bertroge,” Gellatly Road, New Cross, §.H. 14
ADVERTISEMENTS of Books and Insects for Sale, or Books wanted will be nserted at a minimum
charge of 2s. 6d. (for four lines). Longer Advertisementsin proportion. A reduction made for a series
Particulars of Mr. Herbert E. Page, ‘‘ Bertrose,”’ Gellatly Road, New Cross, 8.E. 14
Subscribers who change their addresses must report the same to Mr. HI. li. Paau ' Bertrose
Gellatly Road, New Cross, l.ondon, 8.I., otherwise their magazines will probably be delayed.
Desideruta.—Foreign examples, local races, vars. and abs. from a!l parts of the
world of any butterflies included in the British list. Setting immaterial; exact duta
indispensable. Liberal return made.—IV. G. Pether, ‘‘ Thelma,’’? 4, [Villow Bridge
Road, London, N. 1.
Duplicates.—Cinxia, Bellargus, Coridon, H. Comma, Lineola, Galathea, Moneta,
Nupta, and many others. Desiderata.—Blandina, Irish Icarus, Carmelita, Cuculla.
Gonostigma,.Ashworthii, Templi, Australis, Undulata, Smaragdaria, Testacea.—
W. Gifford Nash, Clavering House, Bedford.
Duplicates.—Cinerea ? , fine forms, grey, brown and blackish, Maritima and vars.
Immorata and other East Sussex species.
Desiderata.—Pups». Luteago (Barrettii), Caesia, Albimacula, Alpina, Xanthomista,
Sparganii, Dissoluta (Arundineta), Graphalii. Also imagines of extreme forms Noctus
in fine condition only.—4. J. Wightman, 35, Morris Road, Lewes.
N. American Lepidoptera in papers in exchange for ditto from any part of the world.
J. C. Woodward, Training Ship ‘* Cornwall,’’ Purfleet, Essex.
CHANGE or Appriss.—H. W. Morse, 4, Wortley Road, Upper Armley, Leeds.
Commander J. C. Woodward, Training Ship ‘* Cornwall, ” Purlleet, BSG
J. H. Durrant, from 17 to 20, Burstock Road, Putney, S.W.
R. S. Bagnall, F.H.S. clo F. Milton, 30-31, St. Swithin’s Lane, H.C. 4.
MEETINGS OF SOCIETIES.
Entomological Society of London.—41, Queen’s Gate, South Kensington, S.W.7,
8 p.m. March 5th, March 19th, 1924.
The South London Entomological and Natural History Society, Hibernia
Chambers, London Bridge. Second and Fourth Thursdays in the month, at 7 p.m.
February 28th, W. J. Lucas, B.A., ‘‘The caudal lamellae of the Naiads of the British
Agrionid Dragonflies. Fon. Sec., Stanley Edwards, 15, St. German’s Place, Blackheath,
8.E.3.
The London Natural History Society (the amalgamation of the City of London
Entomological and Natural History Society and the North London Natural History
Society) now meets in Hall 40, Winchester House, Old Broad Street H.C.2, first and
third Tuesdays in the month, at 6.30 p.m. Visitors welcomed. Hon. Sie W. E.
Gurea, 44, Belfast Road, N. 16. >
All MS. and editorial matter should be sent and all proofs returned to Hy. J. Turner,
98, Drakefel! Road, New Cross, London, §8.H.14
We must earnestly request our correspondents Nor to send us communications IDENTICAL
with those they are sending to other magazines.
lists of Dupnicarns and-Drsgipmrara should be sent direct to Mr. il. KH. Page,
Bertrose, Gellatly Road, New Cross, §8.E. 14
\
OVA, LARVAc, AND PUPAE.
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H: W. HEAD, Giitomrolanist,
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Kull List of Ova, Larvae, and Pupae, also Lepidoptera, Apparatus, Cabinets
etc., sent on application.
Many Rare British Species and Good Varieties for Sale.
MOUNTING
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BACK VOLUMES OF
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Genus Acronycta and its allies.—Variation of Smerinthus tiliae, 3 coloured plates—
Differentiation of Melitaea athalia, parthenie, and aurelia—The Doubleday collection—
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CONTENTS.
PAGE.
Teratological Legs in Lepidoptera, H. A. Cockayne, M.D., F.R.C.P., F.E.S. (with Plate II.) 83
New British Cecidomyiidae, R. S. Bagel Jad beens Oey OR IS\3 eo and J. W. H.
Harrison, D.Sc., F.R.S.Ed. .. fi cS Ae we 36
The Variation in Larentia (Thera) variata, Schitf.. Carl “Hofer. oe 39
Current Notes anD SHort Notices .. a zi oe A S SO 3 41
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TERATOLOGICAL LEGS IN LEPIDOPTERA. 33
Teratological Legs in Lepidoptera. (IVith Plate IT.)
By E. A. COCKAYNE, M.D., F.R.C.P., F.E.S.
Descriptions of abnormalities in the structure of the legs of Lepi-
doptera are few in number. It is probable that they are rarer than in
Coleoptera, in which the legs are more exposed to injury during the
pupal period. But frequently they must be overlooked, owing to the
fact that they are concealed by the wings, by the long hair on the
abdomen, and by their own covering of scales. Specimens of Smerin-
thus ocellatus and Plusia iota, each with an extra leg, have been
described by Schultz and Bleuse. An extra tarsus has been recorded
in Cosmotriche potatoria by Barrett, in Catocala nupta by Chapman, in
Parnassius apollo by Bleuse, and in Ocneria dispar by Forbush and
Fernald. A Aygaena anthyllidis described by Chapman affords the
only example of reduplication in a lepidopterous leg which follows
Bateson’s Law. It has three tarsi on the left meta-thoracic leg, the
two extra ones being arranged in secondary symmetry. Although the
abnormalities, which I am describing below, are not so striking, I think
they are different from any previously noted. They include a tarsus
with the terminal joint double, tarsi with three claws, and a tarsus with
the claws partially fused at the base, but ending in three and five tips
respectively.
Apocheima hispidaria.—Female. Loughton, bred from a full grown
wild larva. IL., 1923. The tarsus of the left metathoracic leg is very
short, measuring only lmm., the corresponding tarsus on the right side
being 8°75mm. long. It has only three joints, the second of which
bifurcates at the distal end. From the anterior, or internal portion,
arises a terminal joint with two small claws and paronychia. [From
the posterior or external portion, which is more heavily chitinised,
arises a thinner, longer joint formed of very weak chitin, and devoid of
claws, pulvillus, and all the other structures which form the foot.
Hig,
Lastocampa trifolii.mKemale. §. Cornwall. Bred IX., 1923.
The right prothoracic leg has a five-jointed tarsus 4mm. instead of
5mm. long. The terminal joint bears three claws. The plate, from
which the pulvillus springs, is abnormal in shape and lies toward the
outer side. ‘The outer paronychium is small, and is very nearly in the
usual position, but the one on the inner aspect is further out than usual,
and is separated from the plate of the pulvillus by a piece of smooth
chitin. The pulvillus itself, well formed, of black and polished chitin,
is displaced outwards. Of the three claws the central one is obviously
supernumerary, but bears no appearance of being double. The outer
one, on the other hand, is very wide, and may be a fused double one.
If so the specimen may conform to Bateson’s Law. The inner half
of this claw may be a mirror image of the outer, and each may repre-
sent a complete claw, whereas the central claw may be a mirror image
of the inner half of the double claw. The two last would be super-
numerary. The long bristle of the empodium is present, but is
omitted from the figure. Many spines are absent from the ventral
surface of the last joint of the tarsus. Figs. 2 and 3,
Lycia hirtaria.—Female. London.
From a family of inbred larvae, many of which produced weak,
Marc 151m, 1924. ,
84 _ THE ENTOMOLOGIST’S RECORD.
crippled imagines. The tarsus of the right prothoracic leg has only two
joints, and measures 1mm. in length instead of 3°25mm. It has on the
last joint a small narrow pulvillus, two small paronychia, two lateral
elaws and a third abnormally broad claw lying almost midway between
and a little dorsal to them. Its tip is bent upwards. Its width makes
it probable that it is a fused double claw. If so, this may be regarded
as an example of Bateson’s Law. The distal extremity of the last tarsal
joint is slightly longer on the inner and wider on the outer side, and
the latter is probably the side on which reduplication has occurred.
The outer part of the double claw may be a mirror image of the exter-
nal lateral claw and the inner part of a mirror image of the outer.
The external lateral.claw would be the original claw and the double
central claw would represent the two extra ones. In addition to the
tarsus the tibia of this leg is short, being 2mm. instead of 3:25mm.
long. Figs. 6 and 7.
Lasiocampa trifolii.cKemale. §. Cornwall. Bred IX., 1923.
The right prothoracic tarsus is very small, being 1mm. in length,
and has only two joints. The terminal joint is so abnormal that I
cannot identify the different parts. There appears to be one minute
paronychium, but the other one and the pulvillus are absent. It ends
in a most peculiar single claw, which terminates in a sharp point and
a small blunt process, and has another sharp pointed process projecting
from it laterally.
There was another dense chitinous process arising from the ventral
aspect of the last joint at a point much nearer to the base. Thin at
its origin it became swollen distally, and the swollen part was deeply
grooved and ended in two sharp points. J made a drawing of it in
the dry state, but broke it off and lost it when making a microscopical
preparation. Apparently there are two claws, one bifid or trifid and
the other bifid. The penultimate joint of the tarsus has only three
spines. Figs. 8 and 9.
Apocheima hispidaria.—Female. Buddon Wood. W. G. Blatch-
22.111.1895. Canon C. T. Cruttwell’s collection.
Of the six legs four have abnormal tarsi. The left prothoracic
tarsus terminates in two large normal claws, but it has only three
joints, and measures 1-75mm. in length. ‘The left mesothoracic tarsus
measures 2mm., has four joints, and ends in a normal foot. The left
mesothoracic leg has a tarsus 1°8mm. long, with four joints The claws
are fused for about one-third of their length and do not diverge in the
usual way. A lateral view shows that the posterior or internal claw is
partially separated into three by deep grodves and terminates in three
distinct tips, an upper, a middle, and a lower one. (Fig. 4.) The
external or anterior claw is also partly divided by a groove. The upper
part ends in a sharp tip turned inwards at right angles, and the lower
part ends in four separate tips, three of which are bent inwards. (Fig.
5.) The normal claws in this species are much longer, quite separate,
and each ends in a single sharp point turned outwards and downwards.
The spines on the penultimate joint of this abnormal tarsus are reduced
in number to three. The right metathoracic leg has a tarsus with four
joints, measuring 1:'75mm. The last three joints are very short. The
penultimate has a rounded lateral outgrowth, and the last a dorsal
outgrowth ending in two sharp pointed pieces of chitin projecting over
the spines. The remaining two legs are normal with tarsi between 3
and 4mm. long.
TERATOLOGICAL LEGS IN LEPIDOPTERA. 35
Lasiocampa trifolit.—Female,
The left prothoracic leg has a tarsus with four joints, the last three
_ being very short. It has two small but perfect claws. Its length is
3mm., that of the corresponding tarsus on the right side being 5mm.
Apocheima hispidaria.—Female.
The left metathoracic leg has a four-jointed tarsus 3mm. instead
of 4mm. long, and the right prothoracic leg has a three-jointed tarsus
2mm. instead of 4mm long.
A. hispidaria.—Female.
The right mesothoracic leg has a three-jointed tarsus slightly more
than 1mm. in length.
A. hispidaria.—Female.
The tibia of the left mesothoracic leg measures 1°5mm. instead of
vmm. in length. The tarsus is normal.
L. trifolii.—Female.
The left prothoracic leg has single-jointed tarsus devoid of scales,
spines, claws, pulvillus and paronychia.
Lycia hirtaria.—Female.
The right mesothoracic tarsus has five joints but is 8 instead of
4mm. lone.
eietar ia.—Female.
The left metathoracic tarsus has five joints, but is half a millimetre
shorter than the right.
L. hirtaria.—F emale.
The left mesothoracic tarsus has only four joints and one claw is
» missing.
Xanthia ocellaris.—H. Worsley- Wood. Thames Valley.
The right prothoracic tarsus has only two joints and measures
15mm. instead of 4mm, All the structures on the terminal joint are
present but much reduced in size.
Hrannis defoliaria.—KFemale.
The left prothoracic leg has a very thin four-jointed tarsus without
scales or claws.
Fidonia atomaria.—Male. Bred L. W. Newman. X. 1910. Dr.
Chapman’s teratological collection.
The right prothoracic leg is very small but perfect. The following
are the measurements of the two legs in millimetres. R. femur, 1-1,
L. 2:4; R. tibia -5, L. 1-8; Epiphysis of R. tibia -3, L. 1:1; Tarsal
joints R. -9, -5, -36, -24, -4, with claws, Li. 1-8, -6, 5, -3, -52:
From them it will be seen that the greatest reduction in length has
occurred in the tibia and femur.
Barrett, C. G.—Ent. Month. Mag., 1899, Vol. XXXV., p. 270.
Bleuse.— Bull de la Soc. Ent. de France, 1900, p. 52.
Chapman, T. A.—Proc. Hnt. Soc. Lond., 1914, p. lxxxiv., and
Trans. Ent. Soc. Lond., 1917, p. 178.
Forbush and Fernald.—The Gypsy Moth. Report of Massachusetts
Board of Agriculture, 1896, p. 341, pl. h., fig. 8.
Schultz, O.—IJllustr. Wehenschr. f. Ent., 1897, I1., pp. 631-2.
[Melitae maturna. —* Among the specimens taken by Mr. Fison in
the Kngadine, in 1901, is a most remarkable g , in which the middle
left leg is replaced by a tiny wing, having the appearance of the inner
margin of a hindwing with the fringe, about 8mm. in length and 2mm.
in breadth. It is quite detached from the normal wing, which is per-
36 THE ENTOMOLOGISY’S RECORD,
fect without it. It is more curious, as the leg is a true limb, which the
wing structures, correctly speaking, are not.’—G.W.|
=
New British Cecidomyiidae. 5.
By RICHARD S. BAGNALL, F.L.S., F.R.S.Ep., F.E.S., and J. W.
HESLOP HARRISON, D.Sc., F.R.S.ED.
(Continued from Vol. XXXIV., p. 154.)
The present lengthy list of additions to the British Fauna is due to
the unequalled opportunities we have had this year of working
districts producing plants, either new to us or not previously accessible
in any quantity. In particular, our visits to Shropshire and to
Blakeney Point were exceptionally profitable; on the contrary, much
hard work was done in the Norfolk Broads with a minimum of success.
Equally noteworthy was the detection, at points well worked by us in
the past, of such species as Rhopalomyia baccarum, Contarinia fagi and
C. pist.
All of this demonstrates that much remains to reward the labours
of Cecidologists in the British Isles.
Clinorrhyncha tanaceticola, K.
Affecting achenes of Tanacetwm.
SuropsHirReE, near Cross House, October, 1923.
Prolasioptera cerealis, Lind.
On various grasses and cereals, a depression in the stem containing
a yellowish orange larva, concealed under a shining black “scale” or
8 Iba.”
Duruam, Gibside, on Avena, Agropyrum and Dactylis. Also other
records. :
Lasioptera populnea, Wachtl.
A leaf pustule greater in diameter and less convex, or rather of less
depth, than that of Harmandia pustulans.
Suropsuire, Pulley Common, near Shrewsbury, on Populus tre-
mula, October, 1923. Rare.
Rhopalomyia baccarum, Wachtl.
On Artemisia vulgaris. Prominent spherical gall, chiefly situated
at the roots.
Durnam, Birtley and Lamesley, August, 1923. the midge just
emerging. Rarer than in 1922, when it abounded in September and
October.
Stenospatha ertophort, K.
Pale pinkish to orange-yellow larvae, in the leaf- sepa of cotton
grass (Hriophorum spp.).
Scornanp, Bavelaw Moss, September, 1922.
SuropsHine and Crnsmnne, Whixall Moss near IEEE Caos,
19038.
NEW BRITISH CECIDOMYIIDAE. 37
g
Mayetiola lanceolatae, Ribs.
On Calamagrostis lanceolatus, white larvae, usually solitary, in
stem near node, causing a shortening of of the terminal internodes.
Suropsarre, Hencott Pool, near Shrewsbury; not uncommon ;
October, 1923.
Mayetiola calamagrostidis, K.
On Calamagrostis lanceolata, under leaf-sheath, mostly basally,
galling the stem much as M. holct on Holcus.
Saropsarre, Hencott Pool, near Shrewsbury, about a dozen old
galls in one clump; apparently local, October, 1923.
Arthrocnodax coryli-gallarum, Targ-Tozz.
Inquiline in gall of Hriophyes avellanae ; larvae yellow.
Somersetsuire, near Bath, July, 1923.
Suropsuire, Bayston Hill, near Shrewsbury, October, 1923.
Harmandta globuli, Ribs.
On Populus tremula, gall somewhat like that of Al. tremulae, but
smaller in diameter.
SHRopsHire, Pulley Common, near Shrewsbury, October, 1923.
Rhabdophaga ocnliperda, Ribs.
On Salix aurita, slight swelling at base of bud.
Duruam, Gibside.
Jaapiella clethricola, Ribs.
Yellow larvae in twisted leaves of alder (Alnus).
SHRopsHIRE, Shomere Pool, near Shrewsbury; occasionally ; October,
1923.
Perrisia auricomi, K.
Gregarious yellow larvae amongst the seeds, which are swollen, of
Ranunculus auricomus.
NortHuMBERLaND, near Stocksfield-on-Tyne.
Perrisia myosotidis, K.
On Myosotis palustris, flower swollen and remaining closed.
Suropswire, Berrington Pool, near Shrewsbury; a few empty galls.
Norrotx, Hempstead, with larvae.
Perrisia socialis, K.
Perrisia sp. H. 5579. Flower head remaining closed and swollen
somewhat basally ; larvae red; on Hriyeron acris.
SHropsuireE, Harley Hill, near Much Wenlock, October, 1923.
Perrisia subterranea, K.
On Silene maritima, in swollen buds formed from reduced leaves
exposed at sand level.
Norrouk, Blakeney Point.
38 THE ENTOMOLOGIST’S RECORD.
q
Contarinia pisi, Winn.
In flowers, shoots and pods of cultivated peas; whitish gregarious
' larvae. Has been recorded by other writers as Diplosis pisit, Kalt. ~
NorTHUMBERLAND, Hexham.
Norrouk, Baconsthorpe.
Contarinia fagi, Rubs.
Beech, young terminal leaves malformed; larvae white and
gregarious.
Scornanp, near Abbotsford.
NortHumpBertanp, Hexham and Corbridge.
Norrorx, Cromer and Hempstead.
Contarinia schlechtendaliana, Rubs.
Sonchus oleraceus, flower heads closed, swollen and deformed; larvae
vitelline, gregarious and leaping.
Norroux, Baconsthorpe. Rare.
Sitodiplosis mosellana, Gehn. (aurantiaca, B. Wagner).
Orange larvae on rye, affecting ovary, which is arrested in its
development.
Duruam, Gibside.
FEindopsylla agilis, Meijere.
An endoparasite of Psylla forsteri, the larvae living in the
abdomen.
NortHUMBERLAND, Stocksfield-on-Tyne.
Lestodiplosis liviae, Ribs.
Inquiline in gall of Livia juncorum on Juncus spp.
Duruam, near Winlaton Mill.
Hormomyia kneuckeri, K.
At roots of Carex.
Scornanp, Bavelaw Moss, September, 1922, on Carea sp.
Duruam, Sunniside, on Carea goodenowit, rare, October, 1923. In
this latter locality Dichrona gallarum, Hormomyia tuberifica and H.
cornifex occurred in extraordinary profusion, with an occasional H.
frirent.
Amerhapha gracilis, Rubs.
Orange-red to red larvae in deformed galls of Schizomyta pimpi-
nellae on Daucus. The galls lose their seed shape and spines, being
usually smooth and glossy. The larvae may be found full fed in mid-
October, after the larva of Schizomyia has left its gall.
SHROPSHIRE, near Pulley Common, locally plentiful.
(To be continued.)
THE VARIATION IN LARENTIA (THERA) VARIATA, SCHIFF. 39
The Variation in Larentia (Thera) variata, Schiff.
By CARL HOFER of Klosterneuburg (Vienna).
(Translated by H. J. Turner, F.H.S.)
At the meeting of the Zool.-bot Gesellshaft of December 5th, 1919,
I discussed this question and there was inserted in the Proceedings
(Vol. LXX., H. 1-2. p. (19)] in 1920, a summary with the addition of
figures of which the further use was unfortunately not possible, owing
to the subsequent loss of the blocks.
This Larentia species was named nearly 150 years ago by the
Viennese professors Schiffermtiller and Denis in a very appropriate
way as “‘variata.” In the name which this Geometer bears, the fact
of its great variability has been well retained. Unfortunately we
possess neither a description nor a figure of that form, which the
authors had in front of them for their determination in 1776[5]. But
since variata is indigenous near Vienna, we have a well-founded right
to take for the so-called stem-form, that form, which occurs as the
commonest in our neighbourhood, as the original type, of which we
are accustomed to take into consideration the extreme variability of
the colour markings. The first figure of vartiata which we find under
fig. 293 in Jacob Hubner’s work issued in 1785, represents this form
tolerably well. Among the material lying before me, consisting of
some 500 specimens from Lower Austria, many examples agree very
well with this figure, and I chose some of these and placed them at
the top of my series which I exhibited.
First of all concerning the variation in colour, I must mention the
following forms :—
ab. nigrofasctata, Gmppbe.—In his work Syst. Bearb. der Spanner
der nérdl. gemdss. Zone,’ 1887, von Gumppenberg established this
form with the short diagnosis ‘‘ Area media nigra,” as a variety. He
refers it to Rossler, who in his ‘‘ I’n. des Rey. Bez. Wiesbaden” in 1881
writes of variata, ‘‘ There isa variety, not figured, with black median
area, while the remainder of the forewing is greyish, white, or wood-
colored.” Réssler himself refers again in the year 1866 in his Verz.
Schm. Herz. Nassau to this variety with black median area, but without
giving it a name.
As a synonym of ab. nigrofasciata, Gmppbg., ab. medionigricans,
Reutti, has been recognised, of which the latter author writes in his
Uebers. Lep. Gross-herz. Baden, in 1898 as follows, ‘“‘ Brownish white,
with unicolorous blackish median area.’’ I have before me two males
and two females of ab. nigrofasciata.
ab. scotica, Stder.—This form was described by Staudinger as a
dark, Scottish, local form of variata and as an aberration occurring in
Central Italy. Prout in Seitz, placed this quite noteworthy form
under obeliscata and determined it as a synonym of ab. obliterata,
B. White. He did this in spite of his having announced in a con-
tribution by himself appearing in August, 1912, in the H’nt. concerning
the English variata, the occurrence of our typical continental form in
England, so that already, the appearance of a dark variata race in
Scotland as mentioned by Staudinger, was undoubtedly established.
The occurrence of true variata appears to have been reported in
England, as in Vol. 46 of the Ent. for 1918, and established over and
40 ; THE ENTOMOLOGIST’S RECORD.
over again by breeding from larvae found on pine (See Notes by
C. E. Raven of Cambridge).
I have before me two males and one female of this form to which
the description of Dr. Staudinger exactly applies. Moreover Herr Dr.
Schawerda has allowed me to examine from his rieh collection an
example of ab. scotica from Kngland, which I pronounced as our native
ab. scotica. This form also agrees well with the figure given as a male
on plate 8 in Seitz, and the placing of ab. scotica, Stder., to obeliscata
may in all probability be considered as correct. At the same time I
can establish ab. obscura as the darkest of our variata forms,.as well as
an aberration of the Wienerwald.
[Since the above was written, I again considered the specimen from
Dr. Schawerda’s collection, and since it was an old and somewhat
damaged example and really difficult to recognise, | doubted whether
it could have exactly the same appearance as true var. scotica, and
endeavoured to obtain some actual and perfectly true examples from
Scotland. In 1928 I succeeded in getting these and at once saw that
var. scotica, Stdgr., was indeed the more or less dark -form of the
(brown) L. obeliscata and not of the (greyish) L. variata. The few
true var. scotica | now have before me are very fine examples of English
melanism and I much doubt whether similar typical scotica have been
found on the Continent. I do not know a Continental fauna which lists
this form. Count Turati has written to me that neither scotica nor any
transitions to it are in his extensive collection from either Central or
any other part of Italy.
It therefore arises that the dark, uniform, greyish-black form of
our &. variata which I wronely considered to be Staudinger’s var.
scotica is unnamed, and at the meeting of the Zool.-bot. Gesell. Wien
on January 4th, 1924, I introduced it as Larentia variata, Sehitf., ab.
obscura, clearing up the matter.—C.H.]
Var. cembrae, Kitt. The appearance of a form analogous to var.
cembrae Kitt., among our Wienerwald variata is interesting. | have
three examples before me, which in their uniform mouse-grey colour
agree fully with the type of var. cembrae from the Tyrol, according to
an examination of the few in the Hofmuseum by Prof. Kebel and my-
self. The specimens before me—all females—descended from an
equally monse-grey female obtained by me in the summer of 1921 at
Rekawinkel, which, since it was already worn, I reserved for egg-laying.
This @ , enclosed in a linen kag, was fastened in a pine tree in the open,
and the larvae grew up therein splendidly. At the beginning of
September, besides quite small larvae, a few pupae were found, which
in the middle of September, gave me a partial 2nd generation, to which
the three specimens I have, belong. But these are distinctly smaller
than the type-form found in the Hofmuseum.
Herr Prof. Kitt describes this form in the Proceed. zool.-bot.
Ges. October 4th, 1912. He considered it a high-elevation form,
living on the stone pine and says of it. ‘ All the wings are pure grey
without brownish suffusion which otherwise occurs in variata. The
disposition of the markings are as in typical variata, the central area
darkened.” But, in Seitz, Prout writes var. cembrae, Kitt is probably a
synonym of ab. nigrofasciata, Gumppenberg; but Kitt describes the
SOCIETIES. 4]
ground colour as pure white, without brownish suffusion.’’ Hence
there must arise to the readers of this work a perfectly false idea of
var. cembrae, and it is incomprehensible why Prout has given the
ground-colour white.
Fritz Hoffmann in his Styrian auna aceepts the wrong description
of Seitz, for therein he gave the pure white ground as the distinguish-
ing characteristic of var. cembrae and then arranged his other forms
accordingly.
From the examples of ab. nigrofasciata and var. cembrae before me it
is seen how distinct these two forms are from one another.
It is probable that var. cembrae is a synonym of var. coniferata,
Curt., which is also described as grey. Var. coniferata has also been
obtained by Miller-Rutz at Griiben in Turtmantal in Switzerland.
P (To be continued.)
G\URRENT NOTES AND SHORT NOTICKS.
We regret to record the death at the ripe age of 84 of Mr. A. H.
Jones, who from 1904 to 1917 was Treasurer of the Entomological
Society of London. For 30 or more years he was a familiar figure in
the meetings at Chandos Street‘ a genial and kindly gentleman. The
robust health, which he enjoyed almost to the end, enabled him to
journey to many parts of Europe in search of rare butterflies until
quite late in life. At the age of 74 he went to Sarepta, on the Volga,
in §. Russia, to become acquainted with the interesting and peculiar
forms which exist in that rich and remote area. We understand that
his collection of European butterflies is bequeathed to the Hope
Museum, Oxford.
SOCIETIES.
Tue HNromonocicaL Socrery or Lonpon.
January 16th, 1924.—Annua Merrtinc.—Mr. E. Hi. Green,
President, in the chair.
Dr. H. Eltringham read the Report of the Council, which was
adopted on the motion of Commander J. J. Walker, R.N., seconded by
Mr. Stanley Edwards.
Mr. W. G. Sheldon, the Treasurer, read his Report.and gave some
details of the highly satisfactory condition of the Society. ‘he Report
and Accounts were adopted unanimously on the motion of Mr. G. T.
Bethune- Baker, seconded by Mr. W. J. Kaye.
The President announced that the Fellows nominated as Officers
and Couneil for the ensuing year had been duly elected in accordance
with the Bye-Laws.
The President then read his Address on ‘“‘Some Hpisodes and
Aspects of Insect Life in Ceylon,” and at its conclusion a vote of thanks
to the President, coupled with a request that it might be printed in the
Proceedings, was moved by Professor EK. B. Poulton, F'.R.S., seconded
by Mr. K. G. Blair, and carried unanimously.
A vote of thanks to the Officers for their services was then passed
on the motion of Mr. H. Willoughby-Ellis, seconded by Mr. W. Rait-
Smith, and Mr. W. G. Sheldon. Dr. H. Eltringham, and Mr. H. J.
Turner briefly replied.
49 THE ENTOMOLOGIST’S RECORD.
Tue Sours Lonpon EntomonoaicaL Society.
December 13th.—Mr. H. Willoughby-Ellis, of Hampstead, and
Mr. G. Vredenburg, of Maida Vale were elected members.
Mr. H. Main exhibited a whip-scorpion, Phryxus reniformis, sent
by Dr. Withycombe from Trinidad, an Arachnid nearly related to the
true scorpions.
Mr. Sevastopulo, Pyrameis atalanta with the second sub-apical spot
missing ; an asymmetrical Abraxas yrossulariata, right forewing
normal, right hindwing traces of a yellow band, left forewing with
yellow patch only, left hindwing with three extra black spots.
Mr. Rayward, H’pirrita (Oporadia) autumnata and FE. dilatata, and
pointed out their distinctions, referring to preparations of the genitalia;
he also exhibited Anaitis playiata and A. efformata and by preparations
showed the complete distinction of the species.
Mr. R. Adkin, a bred series of Arctia villica and read notes on its
occurrence at Eastbourne, its breeding, its parasites and the variation
the specimens showed. Compared with 4. caja it was quite common
in the larval state.
Mr. Andrews, the very rare Dipteron, Aygathomyia elegantula from
Farningham, September 1st.
Mr. Parker, an absolutely black form of Aphantopus hyperantus ;
one of a rich mahogany colour ; a radiated Brenthis euphrosyne ; a rich
chocolate-coloured Mimas tiliae, and Huchloé cardamines 2 with streaks
of orange.
Mr. Blenkarn, a long series of aberrations of British Coleoptera
including a form of Apion aestivum (trifolit), var. ruficrus, with dark
yellow legs, and black tibiae, which was new to Britain.
Mr. Adkin read a report of the Meeting of the British Association
at Liverpool, which he attended as a delegate of the Corresponding
Societies Section.
Subsequently a Special Meeting was held when after a short state-
ment it was unanimously agreed to raise the ordinary subscription to
12s. 6d., the country members subscription to 7s. 6d., and the Life
Composition to £8 8s. Od., to cover the increased rent of their rooms.
REVIEWS AND NOTICES OF BOOKS.
‘“Socran Lire Amone tHE Insecrs.”—(Continued from page 32.)
1. The structure and behaviour of these two complexes show that
they must have arisen from the Parasitic Hymenoptera.
2. The groups of social wasps have evolved independently from
primitive solitary Vespoids.
3. Both complexes are primarily predaceous and feed upon freshly
captured insects.
4. The mutual exchange of food between adults aud their young
(‘‘ Trophallaxis’’ of Wheeler) can be observed more clearly in the
social wasps than in other social insects.
5. The study of wasps and their ancestors furnishes a key to par-
thenogenesis and dominance of the female sex (gynarchy) in the whole
group of stinging Hymenoptera.
REVIEWS AND NOTICES OF BOOKS. 43
6. The first gradual development of a worker cast, of polygyny, and
swarming, is witnessed in the social wasps.
7. Wasps exhibit a high degree of modifiability of behaviour and
an extraordinary development of memory. Notwithstanding some
exaggeration whieh has occurred, Wheeler considers that “ the wasp’s
psychic powers, compared with those of most other insects, or even of
many of the lower Vertebrates seem to me, nevertheless, to be suffi-
ciently remarkable.”
All these generalities are then more closely examined, and a
thorough account is given of the life-history and habits of many
solitary, parasitoid, and social wasps. A fine Phylogenetic Tree of the
various genera and families of Vespoids is given on page 71. On page
55 a beautiful illustration is given of Sphew wrnarius using a selected
pebble to pound down earth over the burrow. On this remarkable fact
Wheeler writes:—‘‘This astonishing behaviour, which has been
observed by no less than nine investigators, can hardly be reduced to
simple physiological reflexes.”
In conclusion he points out that the Vespinae and most of the
Polistinae are monogynous, their colonies being annual developments
begun by a single fecundated queen, and that they perish at the end of
the season, with the exception of the annual brood of queens, which
after fecundation hibernate and start new colonies during the following
spring. Many tropical Epiponinae (and Ropalidiinae) are polygynous
and send off swarms to form new colonies. This behaviour is evidently
as perfect an adaptation to the continuously favourable food and
temperature conditions of the tropics, as is that of Vespa and Polistes
to the pronounced seasonal vicissitudes of the temperate regions.
Wheeler supports the view that polygyny is the more primitive
condition, and as he justly says the species of Vespa and Polistes each
year produce a swarm of females and workers, but that the advent of
cold weather destroys the less resistant workers and permits only the
dispersal queens to survive and hibernate till the following season.
Lecture III. <‘ Bees Solitary and Social.” —This lecture is divided
‘into two parts. The author first discusses man’s interest in the honey-
bee in pre-historic times, and he informs us that the price of strained
honey some 3,500 B.C., in Egypt under the Pharaohs, was five cents a
quart! Many of the innumerable myths and superstitions are recorded,
and it is pointed out that the very abundance of literature—the Bureau
of Entomology at Washington has a working bibliography of 20,000
titles on the honey-bee—is an obstacle to the clear understanding of
this insect. Less than 5% of the bees from all parts of the world are
social, these consist of about 500 species and are contained in only five
genera—T'riyona, Melipona, Bombus, Psythirus and Apis. Bees taken
as a whole may be regarded merely as a group of wasps which have
become strictly vegetarian, and feed exclusively on pollen and nectar
of flowers. It is noted that very many flowers have been modified in
structure, arrangement, colour and perfume, in adaptation to the bees,
and for the purposes of insuring cross-pollination ; and the adaptation
of all the organs and habits of the bees to flowers are described. It is
pointed out that many of the solitary species tend towards social
habits, as in Halictus, Allodape, etc. The following remark taken
from Dr. Hans Brauns is well worth repeating :—‘‘ Most of the descrip-
tions drawn from single captured specimens have little value. Fanati-
44 . HE ENTOMOLOGIST’S RECORD.
cal describers, merely make the work of the monographer more
difficult, or more unattractive, or even well nigh impossible, in a genus
which is almost as monotonous as Halictus.”
An account of many solitary species is given; and then the bumble-
bees are dealt with very thoroughly. They are shown to be very
primitive and to represent an interesting transition from the solitary
to the social forms.
Part 2 is devoted first to the Meliponinae, or stingless bees (the
latter name being not strictly accurate, because a vestigial sting is
present); their habits, etc., being discussed in a most interesting
manner. Finally, to quote an earlier remark in this lecture, the honey-
bee is relegated to its proper piace at the end of a large series of
developments.
In conclusion Wheeler refers to the absence of that peculiar inter-
change of nutriment between the adult and larva, or ‘‘'‘Trophallaxis,”’
which constitutes a powerful factor in maintaining the colonies of
the social wasps. He suggests that the abundant storage of food may
be one of the reasons why such exchanges of nutriment as we observe
among the social wasps and see again in a more exaggerated form
among the ants (as discovered by himself) and termites, were either
never developed or were long ago discontinued by the social bees.
Lectures IV., “Ants, Their Development, Castes, Nesting and
Feeding Habits,” and V., ‘“ Parasitic Ants and Ant Guests,” are, as
their titles show, devoted to the study of ants and their habits. It is
no exaggeration to say that these two lectures comprise, in a compact
form, almost everything that is known about these most interesting of
all insects, from the earliest times right up to date. The subject, more-
over, is developed and expounded in a most able and entertaining
manner. Wheeler gives a summary of what he conceives to be the
fundamental peculiarities of ants. Space will only allow us to briefly
mention the salient points.
The whole family Formicidae consists of social insects. The num-
ber of described species of ants is approximately 3,500. Ants are the
dominant social insects. Their geographical distribution is world-wide.
All authorities agree that ants had their origin among the Scolioids,
an offshoot of the primitive Vespoids. Ants are eminently terrestrial
insects. All three castes (male, female, and worker) are more highly
specialized than in the social wasps and bees. Ants are singularly
plastic in their nesting habits. The young are not reared in separate
cells, but in clusters, and lie freely in the chambers and galleries of the
nest. Their intimate acquaintance with their young, in all stages, has
been an important factor in the development of the Formicidae. As a
group they feed on an extraordinary range of substances. ‘This plas-
ticity in nesting and feeding habits has resulted in the formation of a
vast and intricate series of relationships between ants and other
organisms, including man.
The seven subfamilies of the Hormicidae:— Ponerinae, Cerapachy-
inae, Dorylinae, Pseudomyrminae, Myrmicinae, Dolichoderinae, and
Formicinae—are shown to be clearly established, and an ingenious
figure of an ancestral tree, showing the phylogenetic relations of the
family as a whole, is given. The different kinds of workers and females
are described ; the various methods of colony founding are discussed ;
REVIEWS AND NOTICES OF BOOKS. 45
and the feeding of the larvae, including his celebrated discoveries of
the feeding of the larvae of Psewdomyrminae with the pellets rejected
from the infrabuccal pockets of the adults, and the mutual feeding
(trophallaxis) of larvae and adult are explained.
The carnivorous habits of some of the more primitive species; the
association with plant-lice, etc. ; the very interesting honey-ants, who
have hit upon the ingenious device of using the crops of certain of
their workers to act as living honey-pots; the harvesting ants, who
collect and store seeds; and the extraordinary group of mushroom
growers, all receive due attention.
The seeond lecture on ants is devoted to parasitism, both on and by
ants ; the author preferring the word “‘parasitoidism.” The following
table is given for the Relations of ants to other organisms :—
I. Social Parasitism. (Ants as Parasites.)
A. Compound Nests. (Broods reared separately.)
*J. Brigandage. (Cleptobiosis.)
*2. Thievery. (Lestobiosis.)
3. Neighbouring. (Plesiobiosis.)
4. Tutelage. (Parabiosis, Phylacobiosis.)
5. Hospitality. (Xenobiosis.)
B. Mixed Colonies. (Broods reared together.)
*1. “Slavery.’’ (Dulosis.)
2. Temporary Social Parasitism.
3. Permanent Social Parasitism.
Il. Myrmecophily. (Ants as hosts.)
*Ll. Persecuted Intruders. (Synechthrans.)
Indifferently Tolerated Guests. (Synocketes.)
Mess-mates. (Commensales.)
. True Guests. (Symphiles.)
. External Parasites. (Hctoparasites.)
. Internal Parasites. (Hntoparasites.)
III. Trophobiosis. (Relations of Ants to Phytophethora, etc.)
IV. Phytophily. (Relations of Ants to Plants.)
It is truly remarkable how very much information, on nearly all
the above associations, the author has been able to compress into the
space of_one lecture. This subject has occupied the greater part of our
own study and attention during the last thirty years, and we can only
feel unbounded admiration for the able manner in which Prof. Wheeler
marshals his facts. We do not quite agree with all the theories
advaneed by him, but that again, as we mentioned before in the begin-
ning of this review, is only a matter of personal opinion, and need not
be enlarged upon.
Lecture VI. The Termites or “ White Ants.” The title of this
lecture is as above, but the other two of the most ancient and primitive
orders, the Dermaptera and the EKmbidaria, are first dealt with. The
third order, the Isoptera, which of course consists of the termites,
coming last.
The Dermaptera, or earwigs, are ineluded among the subsocial
> Or OD DO
* Each series, including the myrmecophiles, begins with predatory (indicated
by asterisks), and terminates in definitively parasitic, relations.
46 THE ENTOMOLOGIST’S RECORD.
insects, because the female carefully guards, rearranges, and licks her
eggs, and even remains with the young for a short time after they
hatch.
The Embidaria are a very small order of even more archaic habitus
than the earwigs, and are confined to the tropics. They live in small
colonies in peculiar silken webs which they spin in cavities of the soil,
under stones, and on the bark of trees. The female shows very marked
solicitude for the welfare of her offspring after her first eges have been
deposited.
What is known of the habits of both orders is described; in both
there is a feeble tendency to a social organisation like that of the dung
beetles ; and they are interesting mainly as showing that social ten-
dencies may have been rather prevalent among the ancient carboniferous
orders.
The social organisation of the Isoptera, or Termites, is considered
to be of unusual interest, both because it is so elaborate, though exhibi-
ted by insects of a very primitive anatomical structure, and because it
parallels in so many of its features the social organisation of the most
highly specialized Hymenoptera. The order is naturally divided into
four families, the Mastotermitidae, Protermitidae, Mesotermitidae, and
the Metatermitidae. All the species are social, and the four families
show a progressive development in all ways from primitive to specialized
forms, in the order mentioned. Wheeler regards the termites as primi-
tive cockroaches; he refers to the fossil forms, and traces their descent.
The vast numbers that occur in the colonies of the more specialized
forms are mentioned, and they are shown to be both extremely helpful
and extremely injurious. He carefully characterises the five castes, the
first three of which are fertile and the last two sterile. These are
briefly :—
1. First torm adults: Kings and queens. Deeply pigmented; large
compound eyes, brain, frontal gland; well developed reproductive
organs and wings. ‘The latter break off at their basal sutures.
2. Second form adults: Substitutional kings and queens. Less
pigmented ; smaller compound eyes, brain, frontal gland, and repro-
ductive organs; wings incipient.
3. Third form adults: Also substitutional kings and queens.
Searcely pigmented; brain small; eyes and frontal gland vestigial ;
reproductive glands smaller; entirely wingless.
4. Workers: Unpigmented ; brain small; eyes and frontal gland
extremely small or absent ; reproductive organs embryonic ; wingless.
5. Soldiers: Head large and somewhat pigmented; brain very
small; compound eyes vestigial; wingless. This form varies in
different genera.
The sequence of these forms also varies in some of the families,
and it is noted that there are males and females (unlike the ants) in all
the castes ; some sixteen different kinds of individuals being present,
though probably no single colony ever produces all of them. The
origin and meaning of these various castes is touched upon, and it is
noted that probably all of them may be distinguished at the time of
hatching. All the various problems arising out of this extraordinary
state of things are discussed, and the author remarks, ‘“. . . we shall
have to revise our views on caste differentiation in the ants. It is, in
fact, not improbable that the caste of a particular ant is likewise de-
REVIEWS AND NOTICES OF BOOKS. 47
termined in the egg, but special feeding of the larva may be necessary
to bring it to maturity. The passively fed ant-larvae are certainly
very different from the active termite nymphs, which soon after hatch-
ing are able to run about and seek their own food.”
The social functions of the various termite castes; the dispersion
flights; colony founding; different kinds of nests and nest building ;
and the extraordinary fact that they also grow fungus, as do the ants,
are all described and figured.
Finally the various associations of termites with alien insects pre-
senting a striking parallelism with the condition in ants, though with
some significant differences, are related. The most characteristic
feature is the extraordinary physogastry, or excessive enlargement of
the abdomen in many of their guests, belonging to different orders. Of
perhaps more importance to the lives of the termites than the above
guests, are the numerous intestinal infusoria, which have been found
to be present in so many species, and which are considered to assist
these insects in digesting crude cellulose. In his concluding remarks
Wheeler points out that the amount of degeneration accompanying
social evolution is much greater than in the ants, and this degeneration
is brought about very largely by an increasing need of protection.
As an aid to the reader who may care to extend his studies of the
social insects, the author has added a documentary appendix contain-
ing considerable bibliography and several notes on special topics which
could not be adequately treated in the lectures.
We may add he has done this in a very thorough and generous
manner.—Horace DonistHorrPE.
Tue Procerpincs oF THE SoutH Lonpon EntomenocicaL AND
Narurat History Society, 1922-1923, pp. xxviil-152. With eight
Plates.—Upon comparing this Volume with its immediate predecessors,
seven of which lie before us, we notice at once with great satisfaction,
that this is larger than the largest, showing that the years of depres-
sion following the War Period are passing away, and that more normal
conditions have been restored.
This evidence of recovery, and progress, is to be found also in the
increase. in the number of members, from 200 last year, to 225, in spite
of the loss of 5 by death, and 7 by resignation.
The Treasurer puts the financial position thus—-‘‘ We are still
over £20 short of being in a self-supporting condition.” This is
healthy, but would be better still if the 28 “slow payers” could be
induced to remember their obligations.
The 50th anniversary of the Society did not pass unmarked. A
Supper was held at the Holborn Restaurant, in commemoration of
the event ; a social gathering which emphasizes the happy comrade-
ship which has always marked the ‘South London,” and we are
pleased to read that the result of the venture was a very satisfactory
addition to the funds. A delicate attention was also paid to a, if not
the only, surviving Founder of the Society in 1872, Mr. G. C.
Champion, by electing him an Honorary Member.
Six of the papers read at the Meetings are printed in full. An
unusual local list ‘‘ Spiders found in the Neighbourhood of Oxshott,”
but extended to the whole County of Surrey in an accompanying list,
is contributed by Mr. W. S. Bristowe. This carries on the work of
48 THE BNTOMOLOGIST S RECORD.
O. P. Cambridge, who however it must be remembered never professed
to exhaust the Fauna of this particular district. Of the 244 Species
listed, 50 have not been recorded hereabouts previously, and one,
Oonops domesticus, in the male sex, was previously unknown to
Science. ‘To his paper Mr. Bristowe adds a complete list of all the
Species of the nearly related Phalangidae, and ‘‘ Pseudo-Scorpions ”
taken. This Paper is illustrated by two Plates.
Mr. HK. E. Green follows with “A Brief Review of the indigenous
Coccidae of the British Islands.” This, which is accompanied by four
Plates, includes all the Species yet recorded in Britain, with
descriptions, and life-histories, so far as are known.
Mr. R. Adkin gives a very interesting account of ‘The Lepi-
dopterous enemies of man.” Quoting Dr. L. O. Howard’s remark
upon ‘the enormous forces of injurious insects which attack man at
every point, and constitute to-day his greatest rivals in the control of
Nature,’ Mr. Adkin gives interesting details as to the tremendous
destruction wrought by these tiny adversaries.
The same contributor gives ‘a History of Diacrisia mendica, and
its varieties,’ a complete monograph of the insect.
Mr. W. J. Lucas supplies notes upon the mouth organs of the
Paraneuroptera (Dragon-Flies), a further contribution to his well
known studies in this group of insects.
Mr. T. H. Ul. Grosvenor continues his work amongst the
Zygaenidae, touching upon the evidence of the working of the
Mendelian Law, in the rearing of these insects from selected parents.
He finds that confluence of spots, does not follow the law, and
ascribes this rather to temperature, and atmospheric conditions. He
records also his experiences, and disappointments, in rearing, the
treatment which has proved most successful during the very critical
period of hibernation, the food plants, and distribution. He
mentions, in connection with the extreme vitality of these insects,
their ability to resist the “Cyanide Bottle,” which power it recurs
to one, is shared with the butterfly Genus Acraea, at least in South
Africa.
The President’s Annual Address is an accoant of his experiences
during a trip to Canada, entitled, ‘‘ Some Notes on the Natural History
of Manitoba.” This reminds us of our experiences in that country
many years ago, and we are not at all surprised to find him complain-
ing about the attentions of the ‘‘ Mosquitoes,” which would appear to
be as abundant and persistent, asever. Whether these pests will ever be
exterminated remains to be proved. Pinning Microlepidoptera, with
head and arms inside the net, and enveloped in the sometimes far from
fragrant smoke of the inevitable ‘‘ Smudge,”’ is not an easy business.
The ‘‘ Abstract of Proceedings’ contains a wealth of interesting notes.
Three Field Meetings were reported, more encouraging it would appear
than those of the previous year, when these ‘‘outings” were spoiled,
we remember by unfavourable weather conditions.
Copious Indices, both General and Special, are provided, occupying
nearly twelve pages.
The Proceedings include the report of the Society’s Delegate
(Mr. R. Adkin) to the meeting of the British Association at Hull.—
C.R.N.B.
Subscriptions for Vol. XXXVI. (10 shillings) should be sent to
Mr. Herbert E. Page, ‘‘Bertrose,”’ Gellatly Road, New Gross,
S.E.14 [This subscription includes all numbers published from
January 15th to December 15th, 1924.)
Non-receipt or errors in the sending of Subscribers’ magazines should be
notified to Mr. Herbert H. Page, “ Bertrose,” Gellatly Road, New Gross, $.E. 14
ADVERTISEMENTS of Books and Insects for Sale, or Books wanted will be nserted at a minimum
charge of 2s. 6d. (for four lines). Longer Advertisementsin proportion. A reduetion matle for a series
Particulars of Mr. Herbert H. Page, ‘‘ Bertrose,’”’ Gellatly Road, New Cross, §.H. 14
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Gellatly Road, New Cross, liondon, S.H., otherwise their magazines will probably be delayed.
Desiderata.—Foreign examples, local races, vars. and abs. from all parts of the
world of any butterflies included in the British list. Setting immaterial; exact duta
indispensable. Liberal return made.—IV. G. Pether, ‘Thelma,’ 4, Willow Bridge
Road, London, N. 1.
Duplicates.—Cinxia, Bellargus, Coridon, H. Comma, Lineola, Galathea, Moneta,
Nupta, and many others. Desiderata.—Blandina, Irish Icarus, Carmelita, Cuculla.
Gonostigma, Ashworthii, Templi, Australis, Undulata, Smaragdaria, Testacea.—
W. Gifford Nash, Clavering House, Bedford.
Duplicates.— Cinerea 2, fine forms, grey, brown and blackish, Maritima and vars.
Immorata and other East Sussex species.
Desiderata.—Pups». Luteago (Barrettii), Caesia, Albimacula, Alpina, Xanthoiista,
Sparganii, Dissoluta (Arundineta), Graphalii. Also imagines of extreme forms Noctue
in fine condition only.—dA. J. Wightman, 85, Morris Road, Lewes.
N. American Lepidoptera in papers in exchange for ditto from any part of the world.
J. C. Woodward, Training Ship ‘‘ Cornwall,’’ Purfleet, Essex.
MEETINGS OF SOCIETIES.
Entomological Society of London. —41, Queen’s Gate, South Kensington, S.W. 7,
8 p.m. March 19th, April, 2nd, May 7th, 1924.
The South London Entomological and Natural History Society, Hibernia
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—Hon. Sec., Stanley Edwards, 15, St. German’s Place, Blackheath, S.E.3.
The London Natural History Society (the amalgamation of the City of London
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Society) now meets in Hall 40, Winchester House, Old Broad Street H.C. 2, first and
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Myrmecophilous Notes for 1923, H. Donisthorpe, F.Z.S., F.E.S. 5.0 : a0 49
New British Cecidomyiidae, R. S. ee F.L.S., F.E.S., F.R.S.Ed., ee I Wo. He
Harrison, D.Sc., F.R.S.Ed. .. Z 56 53
A Society in the High Alps, Névache-le- Chatenae Wm. Heide M. ie ae ‘ : 55
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MYRMECOPHILOUS NOTES FOR 1923, 49
Myrmecophilous Notes for 1923.
By H. DONISTHORPE, F.Z.S., F.E.S.
Most of my time in the field in 1923 was again spent with
researches in connection with Coleoptera. It is possible, nevertheless,
to record a certain number of interesting facts and observations con-
cerning ants and myrmecophiles. I have taken this opportunity in
mentioning any ants, to record when the species in question has been
discovered in any new county or vice-county, since the publization of
British Ants, in 1915. The knowledge of the distribution of our species
has not been added to as much as I should have liked since that date.
IT am hoping that all entomologists, botanists, etc., will be so good as
to send me ants when collecting in the less worked counties. A glance
at the British distribution of the species in my book will show that
many counties are still without records for even some of the commonest
and most widely distributed of our ant fauna.
Formicipar.— Ponerinae.
Ponera coarctata, Latr.—A deilated 2 and five % 3 were found in
a nest of Formica fusca at Box Hill, on May 4th. These were taken
home and put into'a small plaster observation nest; but they unfortu-
nately escaped during my absence from home. As I have before
mentioned (Brit. Ants, p. 70), colonies of this species have not been
kept in captivity with much success. On August 8th afew 8 % were
dug up with seed potatoes at St. Peter’s, Kent. There are no new
county records for this ant.
Myrmicinae,
Myrmecina graminicola, Latr.—A 8% was found in a nest of F.
fusca, aS is often the case, at Box Hill, on May 4th. The only new
county record for this species is Sully, Glamorgan, where it was dis-
covered by Hallett, in 1916. My colony of this ant, which I have kept
in captivity for thirteen years and ten months, continues to flourish
and prosper. No further fighting has taken place, and very few ants
died during the year. February 11th.—The first eggs laid in 1923,
and several of the many larvae present being large (2 ?). February
25th.—The large larvae had pupated and prove to be 9 2. April
22nd.—A winged @ present. May 21st.—Many g and 9? pupae.
May 27th.—A second winged 9. June 24th.—Two winged g g and
five winged 9 ¢. July 38rd._—Many ¢ g and winged 2 ?. August
1st.—All 2 2 had lost their wings. September 30th.—Two large
bunches of eggs in different parts of the chamber, surrounded by many
3 3, many larvae, ¥ pupae, and several g ¢ still present.,
Monomorium pharaonis, L.—On September 26th 8 3 were observed
on the plates at breakfast, at the Park Hotel, Preston, Lancashire
(Mid.). This is a new vice-county record. Other new county records are
—Salisbury, Wilts., S. (O.P. Cambridge Coll.) ; Nottingham, Notts
(Thornley) ; and Dublin, Co. Dublin (Stelfox).
Myrmica scabrinodis, Nyl.—Was found at Wicken in August ; its
first record for Cambridgeshire. Other such records are—Trelleck,
Monmouth (Hallett) ; Church Stretton, Salop (Leman) ; Weedley, 8.E.
Yorks (Stainforth); Bunawe, Main Argyle (Waterston); Hmyvale,
Aprit 15ru.
50 THE ENTOMOLOGIST S RECORD.
Monaghan (Morton); near Kilkenny, etc., Co. Kilkenny (Phillips) ;
Brosna, ete., King’s County (Phillips); Abbeyleix, Queen’s County
(Phillips); Kilrush, etc., Clare (Phillips); and Coolmore, Cork
(Janson).
Myrmica scabrinodis v. sabuleti, Mein.—A dead ¢ was found ina
nest of A. (D.) niger, at Dover, Kent, H., on May 1st, and Hodson sent
me 8 8 to name, taken fighting with M. laevinodis, at Sharpenhoe,
Beds; being new records for these two counties. Others since 1915
are—Flax Burton, Somerset, N. (Bacchus) ; Savernake Forest, Wilts,
N. (Butler) ; Bloxworth, Dorset (O. P. Cambridge Coll.) ; Cavenham,
‘Suffolk, W. (Harwood) ; Loddington, Northampton (S. O. Taylor) ;
Bristol, Gloucester, W. (Bacchus); Trelleck, Monmouth (Hallett) ;
Bewdley, Worcester (Donisthorpe) ; Church Stretton, Salop (Leman) ;
Grassington, Yorks. Mid W. (Butterfield); Howth Head, Dublin
(Stelfox) ; Devil’s Glen, Wicklow (Stelfox) ; and Rosslare, Wexford
(Phillips).
Leptothorax nylanderi, Forst.—A large colony was found at Pad-
worth, on August 81st, occupying the burrows of Priobium castaneum
in av old holly tree in a hedge. Dr. Joy also found the species this
year at Windsor Forest, in an old oak tree, tenanted by A. (D.) brun-
neus. The only new county records are—Bosham, Sussex, W. (Har-
wood); Billericary, Essex, 8. (Box); Chepstow Castle, Monmouth
(Hallett) ; Shrewsbury, Salop (Hodson).
Formicinae.
Acanthomyops (Dendrolasius) fuliginosus, Latr.—On September
80th a number of 8 8 of this ant was swept up in a turnip field near
Colby Glen, Isle of Man: As no trees occurred near by the ants must
have been nesting in the ground. This is a very interesting capture,
on account of the fact that it is the furthest north in which the species
has yet been found in the British Isles ; moreover, all problems con-
nected with the fauna and flora of the Isle of Man are of considerable
importance. The island has been demonstrated to have been covered
with a vast sheet of ice during the Glacial period ; but whether it was
connected with England or Ireland, or both, after the disappearance of
the ice, or whether it was isolated before that epoch, is unknown.
It appears to me that the fortuitous arrival of A. fuliginosus, either
by air or by water, or by human agency, is very improbable. We have
proved that colonies of this ant extend their range by branch nests, or
by the retucn of fecundated ? ¢ after the marriage flight to their own
colonies, or by such ? @ being accepted into nests of A. (C.) mixtus.
The marriage flight takes place on, or near, the parent nest, and the
fecundated ° 9 get rid of their wings at once. It is very doubtful if
they could be carried so far by the winds as the Isle of Man (the
nearest lands are Scotland 16 and 20 miles, Cumberland 30 miles,
County Down 30 miles, Anglesea 45 miles); and even if they were, it
is extremely improbableif such a ? , whois unable to fonnd her colony
unaided, would find a nest of A. wmbratus or A. niatus, eyen if they
occur on the Island, which is at present unknown. Secondly, if by
water she would surely perish; and it is inconceivable that a carton
nest of this species could be drifted over without all the inhabitants
being drowned. This would tend to prove that the Isle of Man was
still connected with the mainland after the disappearance of the ice.
MYRMECOPHILOUS NOTES FOR: 1923. 51
Other new county records for A. fuliginosus are—Wotton-under-Hdge,
Gloucester, E. (Perkins); and Glan Conway, Denbigh (W. Gardner).
A. (Donisthorpea) niger, .—On June 10th, when at Hastbourne,
Mr. Blair picked up on the downs a large gnail shell, occupied by a
small colony of this ant, which he handed to me. On August 4th
marriage flights occurred from several nests in my garden at Putney,
at 4.80 p.m. summer time. August 30th, two solitary dedlated ? 9
-were found in the empty pupal chambers of Criocephalus polonicus,
under bark on pine stumps, at Padworth. After a marriage flight
they must have selected these situations in which to bring up their
brood. This species was abundant under stones on an island in the
river Swale, near Richmond, Yorks, N.W., on August 15th, a new
vice-county record. The only other new records are—Trelleck, Mon-
mouth (Hallett); and Byrford, Hereford (Leman).
A. (D.) alienus, Férst.—This species was very abundant in July at
Hunstanton, all over the sand hills, in flowers, under refuse and stones.
The new records are—Savernake Forest, Wilts, N. (Butler); and
Wallasey, Cheshire (Hallett).
Ap (D.) brunneus, Latr.—It will be remembered that this ant was
discovered in January this year, by Dr. Joy, at Theale, in Berkshire,
and was introduced to the British list by me [Hnt. Record, 35, 21-23
(1923)]. On June 20th we visited the locality again, and found that
the ants had deserted the felled poplar tree in which the colony was
originally discovered. Another colony was found in a hawthorn tree
near by (from it two young @ @, one with one wing and the other
with a wing stump, some 8 8, larvae, and % cocoons were taken) ;
and % 8 were also found on and under the bark of a large oak tree.
The nest, however, of the latter could not be located. Joy subse-
quently discovered the species in Windsor Forest, on oak trees, and
later I also found such colonies there, which could be detected by the
presence of frass outside the bark; but again the actual nests were not
traced, and the ants quickly disappeared. On August 80th I went
again to look at the hawthorn tree at Theale, but the ants had de-
parted. On breaking into the tree, the wood inside was found to be
entirely riddled by the borings of the ants; the colony, therefore,
must have been in occupation for along time. I kept for sometime
in observation nests, some of the ants and larvae from the poplar tree,
and also those mentioned above as being taken from the hawthorn tree;
but it appears to be a cowardly, stupid, and uninteresting species in
captivity. I tried to induce the two colonies to amalgamate without
success; nothing would induce the queenless colony to accept one of
the young queens, she was eventually killed, as were all % % intro-
duced from either colony into the other. The other young queen soon
died in her own colony, and all the 8 8 gradually died off. These
ants frequently ‘“salute’’ each other; they chewed up wood put into
the nest, and would eat a little honey, but not readily. They take a
long time to discover the presence of food when introduced into the
nest ; and when an ant had found it, it did not endeavour to acquaint
its fellows with the fact.
Acanthomyops (Chthonolasius) flavus, F.—Marriage flights occurred
at Wicken, on September 18th, in the afternoon. It occurred abund-
antly at Colby Glen, Isle of Man, in September, under stones on walls,
etc. It was also sent to me from the Island by Mr. 8. O. Taylor; its
first record for the Isle of Man. Other new records are—Trelleck,
52 . THE ENTOMOLOGIST S RECORD.
Monmouth (Hallett); Ystradfellte, Brecon (Hallett); Weedley, etc.,
Yorks, S.E. (Stainforth); Killkenny, ete., Co. Killkenny (Phillips) ;
Maryborough, etc., Queen’s County (Phillips); Birr, King’s County
(Phillips); and Thurles, Tipperary, S. (Phillips).
A. (C.) mivtus, Nyl—% % were taken at roots of grass and under
stones, at Dover, on May 1st. The new records for this species are—
New Forest, Hants, S. (Donisthorpe); Sharpenhoe, Beds (B. 8.
Williams); Mount Garret Wood, Wexford (Phillips); Graiquena-
managh Wood, Kilkenny (Phillips); Maryborough, Queen’s County
(Phillips) ; and Menlough, Galway, EH. (Phillips).
In a valuable paper entitled “‘ Kine interessante Instinktregulation
bei Ameisen (Lasius mivtus, Nyl.),” Wasmann records that he found,
in May, 1923, at Valkenburg, a mixed colony of Lasius fuliginosus and
L. miatus, and he points out at some length the importance of the fact
that both species were seeking food and marching together in files
above ground. As miatus is, when by itself, a very subterranean species,
it shows how it had learnt to break away from its instinctive and
inherited habits. He refers to my paper on the colony founding of
fuliginosus ; and to a similar case as the one above mentioned, when I
found the same two species marching together in Hngland in 1918.
[Att. Pont. Accad. Romana, 16, 255-59 (1923)]. It was on July 17th,
1918, in the New Forest, when I found the mixed colony which he
refers to. Both species were walking together in files along a fence,
near a railway bridge. I mentioned that—“ I found that the tracks
led right down the brickwork of the bridge to the ground beside the
line. It was really a beautiful sight, when the sun was shining, to see
the jet black fuliyinosus and yellow miatus marching in files up and
down the wall of the bridge, and saluting each other when they met.
As miaxtus is very subterranean in its habits, it must have learnt from
the fuliginosus to march in files in the open.” ([Hnt. Rec., 34, 4
(1919) ]. :
Formica rufa, L.—When in Dean Forest, in June, this ant was
found to be abundant, its nests being constructed of grass ; holly twigs
and leaves; and beech buds; respectively. Winged 2 were
observed walking about the roads in the Forest on the 18th and (6th,
and a few dealated ? 2 on the latter date. A 3S was captured on the
wing on the 14th; evidently marriage flights had recently taken place.
It was on June 15th (1911), that I actually witnessed the coupling of
the sexes of this species at Aviemore. New records for I’. rufa are—
Trelleck, Monmouth (Hallett); and Ystradfellte, Brecon (Halleit).
Formica sanguinea, Latr.—On May 26th a number of nests of this
ant was dug up at Woking. In one of these about 7% of the ants .
present were pseudogynes, and over 20 queens occurred, but not a single
fusca slave could be found. This nest was situated in the exact spot
where I first discovered pseudogynes at Woking, in two nests situated
near to each other, on May 12th; 1913; and I have never found them
to be present in any other of the nests scattered over this district.
Indeed I have only once found sanguinea pseudogynes in any other
place in Britain, v7z., in the New Forest, on May 22nd, 1908. The
Woking pseudogyne colony has flourished for ten years to my know-
ledge, and I have recorded visits to it and experiments, etc., in the
years 1913-1918. New records for F’. sanguinea are—Westerham, etc.,
Kent, W. (Harwood); Southend, Essex, 8. (O. Whittaker); Much
*
NEW BRITISH CECIDOMYIIDAE. 53
Wenlock, Salop (O. Whittaker); and Grange-over-Sands (O. Whit-
taker). Whether the last-named locality is in Lancashire or West-
moreland, I know not; and shall be glad of information on the
subject.
Camponotus (Myrmothrix) abdominalis, .—Miss Tassart gave me &
24 and 8 of a var. of this species, which she had found on some
apples in her house at Clapham Common in January.
(To be concluded.)
New British Cecidomyiidae. 5.
By RICHARD S. BAGNALL, F.L.S., F.R.S.Ep., F.E.S., and J. W. |
HESLOP HARRISON, D.Sc., F.R.S.Ep.
(Continued from p. 88.)
[Porricondyla phragmitis, Giraud.]
On Phragmites, small depressions in face of stem, as a rule near the
node, and each containing a single larva under, and therefore covered
by the epiderm.
Suropsuire, Upper Berrington Pool, near Shrewsbury, October,
1928 ; a few examples. The species is entered in square brackets (as
above) in Houard.
We also saw evidence of what may be Lasioptera flewnosa, a species
not yed recorded as British.
Stenodiplosis geniculati, Reut.
This is the Cecidomyidarum sp. we have recorded from Alopecurus
geniculatus.
Cectdomyidarum sp.
Pale pink larvae, at the roots of Carew stellulata.
ScotntanD, Bavelaw Moss, September, 1922.
Cecidomyidarum sp. (2=B and H 400).
Small white larva at base of leaf-sheath of Carea stellulata.
Scornanp, Bavelaw Moss, September, 1922.
Cecidomytdarum sp.
On Rubus fruticosus; leaf crinkled basally, containing creamy-
yellow to pale orange larvae, gregarious.
Duruam, Ravensworth, August, 1923.
Cecidomyidarum sp.
On Betula; parenchymatous leaf gall, not hypertrophied or dis-
colored as in Contarinia betulina.
Duruam, Ravensworth and Gibside, August, 1923.
Cecidomyidarum sp.
On Poa sp; small yellowish larva in the seed.
Dvuruam, Gibside, August, 1923.
54 THE ENTOMOLOGIST’S RECORD.
Cecidomyidarum sp.
On Pyrola rotundifolia var. arenaria: flower remaining elosed,
larvae white.
Lancs., Freshfield, September, 1923.
Cecidomyidarum sp.
On Chlora perfoliata ; flowers remaining small, closed, and some-
times twisted; larvae white.
Lancs., Freshfield, September, 1923.
Cecidomyidarum sp.
On Ballota nigra; crinkling of leaves basally, larvae pale yellow.
Norrouk, Hindolvestone.
Cecidomyidarum sp.
Gall like that of Asphondylia lathyri, in pods of cultivated beans:
larva red.
Duruam, Birtley.
Cecidomyidarum sp.
On Jris pods; twisting the fruit.
YorxsuireE, Hull, September, 1922.
SHRopsHiIRE, Bomere and Shomere Pools, near Shrewsbury, Octo-
ber, 192%. a
Cecidomyidarum sp.
Red to bright orange-red larvae in leaf-sheaths of Catabrosa
aquatica.
SuHRopsHireE, near Kdstaston, October 8th, 1923.
Cecidomyidarum sp.
On Frawxinus; parenchymatous leaf gall-like that of Perrisia
fravinea, but with an irregular purplish-black discolored patch. The
larva is white and is later than P. fravinea, occurring on the same
leaf as the old galls of the latter.
Widely spread but not so common as P. fraxinea.
Cecidomyidarum sp.
On Comarum palustre; pink to blood-red larvae in head.
Norrotk, Hindolvestone.
SuropsHirgE, Bomere and Shomere Pools, near Shrewsbury,
October, 1928.
Cecidomyidarum sp.
On Epilobium angustifolium; a small honey-yellow larva in galls of
the Psyllid Aphalara nebulosa.
SuropsHirE, Shomere Pcol, near Shrewsbury, October, 1923.
Cecidomyidarum sp.
Apparently predacious, feeding upon Sciara larvae under beech
bark.
A LOCALITY IN THE HIGH ALPS. 55
_ Duruam, Gibside, October, 1923.
Cecidomyidarum sp.
Inguiline in juniper gall of Rhopalomyia valerii ; larva yellow.
NortHumBertanp, Helingham, August, 1922.
Cecitdomyidarum sp.
Inquiline in galls of Rhopalomyia baccarum ; larva honey-yellow.
Duruam, Birtley, August, 1922.
Cectdomyidarum sp.
(a) Naked pupa in gall of Jaapiella veronicae on Veronica chamae-
drys.
NortHuMBERLAND, Ratcheugh Crag, near Alnwick, August, 1922.
_ (b) White larva in gall of Perrisia similis on the same plant;
probablyt he same species. —
Scorzanp, Kelso, August, 1923.
Cecidomyidarum sp.
On Anaygallis arvensis ; honey-yellow larvae in seed capsules.
Lancs., Poulton-le-Fylde, October, 1923.
_ New host plant for species already recorded. Jaapiella floriperda,
FE, Loew.
Hypertrophied discolored flowers with pale red larvae on Silene
maritima.
Norrotk, Blakeney Point.
Jaapiella inflatae, Riibs.
With the preceding on Silene maritima.
Contarinia cucubali, K.
White jumping larvae in gall formed from terminal leaf-bud of
Silene maritima.
Norroik, Blakeney Point; much more abundant than the
preceeding.
A Locality in the High Alps, Névache-le-Chateau.
By WILLIAM FASSNIDGE, M.A.
Névache-le-Chateau (Hautes-Alpes), 21 kilometres from Briangon,
P.L.M. Altitude 1595 metres. Autobus service from Briangon in
summer. Staff map 1 : 80,000, Briangon 189 N.K. Hotel de Névache ;
Pension : ‘‘ Les Sapinettes.”’
In such a disappointing season as that of 1923, when, at all events
in the south of England, there was little entomological work possible, ©
one’s thoughts turn with longing to more favoured localities on the
continent, and apologies for this article seem hardly necessary. Most
English collectors have spent the summer vacation in the Alps at one
time or another, but of the large number who visit this “‘ Playground
56 THE ENTOMOLOGIST’S RECORD.
of Europe,” few seem to stay in the same locality for any length of
time, and fewer still seem to get far away from the beaten track. There
is risk attached to this procedure, both with regard to the insects one
may not take, and to the accommodation, which is not always of the
most luxurious in a remote alpine village; but none the less, there is a
decided charm in striking out into the unknown, for there are butter-
flies everywhere in the Alps, and our knowledge of their distribution is
as yet far from complete.
The locality where the writer spent six weeks with his friend Mr.
A. E. Burras, B.A., F.E.S., was the village of Névache, which nestles
in the valley of the Clairé, 21 kilometres from Briangon, the nearest
accessible point on the railway, and about 2 km. from the Italian
frontier. The village is quite one of the highest in France, being about
5,000 feet above sea-level. It includes five scattered hamlets, and had
before the war a population of 422 in the winter months. It is still
practically unknown to the tourist. The valley of the Claré, which
stretches almost due north and south from Briancgon, makes a bend to
the west and widens out before Névache is reached, while beyond the
village the valley rises steadily to the north-west, until the road beside
the torrent degenerates into a mule-track and is almost lost among the
mountains. Few cars attempt to climb beyond Névache, and of those
that do, all return by the way they went. The visitor is completely
cut off from civilisation and can only visit Briancon in the jolting
autobus, that runs in the summer months, on pain of spending at least
one night there. All excursions must be made on foot; there are no
places of interest in the neighbourhood ; the entomologist can give his
undivided attention to the insects that abound on every hand, with no
fear that time will ever lag, rather will he find, as we did, that the days
are all too short.
After such dismal weather in England, it is a pleasure to record
the glorious weather we experienced. We reached Névache at the end
of July, and photographs taken then show fine masses of cloud high in
the sky. After that for three weeks no cloud was seen, and the sun
blazed down from a sky of the brightest blue, scorching up crops where
irrigation was not possible, bringing forth grasshoppers innumerable,
and causing us to shed all but the most essential garments. A sudden
drop in the temperature, followed by 24 hours’ rain, came as a welcome
relief almost, after which the sun regained his power nearly, and the
weather, except for one rainy morning, was fine for the remainder of
our visit. High winds were not infrequent, and thunderstorms were
often reported from neighbouring valleys, indeed almost every evening
sheet lightning flashed above the mountain tops, but no storms came
our way. Yet in spite of the abnormal drought, the countless streams
and springs, fed by the mountain snows, kept the upland pastures
green, and the cascades and torrents foamed and dashed amongst rocks
and boulders almost as impetuously as ever.
From the time of our arrival at the end of July, until the fourth
week in August, insects were to be taken in the greatest abundance,
both in the valley and on the mountain slopes up to the snow-line ;
but as the pastures were successively shorn at-ever greater altitudes,
so the numbers of insects decreased, and a sharp temporary drop in the
temperature round about the 23rd August, wiped out many species and
put a sudden end to insect life at high altitudes. From that date to
A LOOALITY IN THE HIGH ALPS, 57
the end of our stay hunting was restricted to sheltered localities and
favoured spots below 6,000 feet, and most of those species that were
abundant when we arrived, had completely disappeared. We were nene
the less astonished to note how some species seemed to spread their
emergence over the whole period of our stay, while the vast majority
lasted rarely more than three weeks. For instance Polyommatus
(Hirsutina) damon was in full flight on July 80th, and on September
9th it was still possible to take a series in good condition ; Parnassius
apollo was for the most part somewhat worn at the end of July, but
freshly emerged specimens were taken at the beginning of September ;
Melitaea dictynna appeared to have two distinct waves of emergence,
one early in August, the other three or four weeks later. Probably the
most productive time for localities at such high altitudes is from mid-
June to mid-August, but unfortunately holidays are not fixed with any
regard for the entomologist.
Staying as we did for some time in the same place, we were able
to utilise every method of collecting known to us. By day we worked
at flowers—Névache is nearly as famous as a hunting ground for the
botanist—or followed the course of some dashing torrent right to its
source in a patch of snow, rising 4,000 feet, and finding insects in
plenty all the way. Such hot weather as we experienced made of every
seeping spring on the hillside an amazing place of rendezvous for many
species of blues, skippers, and Erebias. For two or three hours round
about mid-day, such species as Plebeius (Latiorina) orbitulus, Plebeius
(Aricia) donzelii and Hesperia alveus settled on the moist ground in
swarms, while the Hrebias seemed more partial to boulders wet with
the spray of the cascade. The runnels, by means of which the villagers
irrigated their fields and gardens, especially where they crossed a dusty
track, were at dusk the resort of numerous Geometers, which could be’
seen in the lamplight greedily imbibing moisture from the damp ground.
Always after a hot day we found large numbers of Geometers ‘around
these wet places, but of Noctuae we only saw three specimens; and
after the drop in temperature already referred to, either the Geometers
ceased to be thirsty, or more probably, they were for the most part ex-
terminated, for we saw very few around the puddles. One Geometer,
Halia brunneata, was to be found by day, drinking at mud-patches
amongst the pine forests that cover the slopes of the mountains on the
southern side of the valley ; and concerning this species we observed a
curious fact: when it first appeared we tried hard to take a series, but
with indifferent success, until we sat down in the shade of the pines to
rest and to wipe the moisture from our brows. Then H. brunneata
began to appear from all directions and to flutter around us in fair
- numbers. Not until we grew tired of taking them did we discover that
they came attracted by the perspiration that covered us, which they
would imbibe from a bare arm until literally driven away. Certain
species which in England sometimes circle round, and even settle upon,
the person, may conceivably be attracted by the same natural bait.
Hvery evening we went for a short stroll in the dusk after dinner,
and hunted with lamps among the flowers upon the hillside. We did
not begin to sugar until nearly a fortnight had elapsed, chiefly because
we were too busy with other methods, and there was no very suitable
sugaring ground in the district. Moreover, conditions throughout our
stay were unfavourable to sugar, so far as we could judge, and for the
58 THE ENTOMOLOGIST’S RECORD.
four weeks or so during which we sugared regularly, we did not once
see more than four insects on any one patch at a time. Of the species
that came to sugar very few were in any numbers, and quite a large
proportion were represented by three or four or even single specimens
only, while others, including Laphygma exigua, of which a few examples
were netted, did not visit the sugar at all. The species taken serve to
show how short the season must be in these altitudes, and how strangely
times of emergence differ from those noted in England, for iate autumn
species were found in mid-August side by side with insects associated
in England with July.
Beating for larvae was almost a complete failure. Although we
persevered after the first check, we never found very many, and of those
we took at least 90% were ichneumoned. The trees and bushes avail-
able were chiefly pines, aspen, willows, juniper, barberry, wild plum,
and alpine rose, and none of them yielded results at all commensurate
with the time and effort expended. Besides, a considerable number of
the larvae taken we could not identify, and in some cases we never
shall be able to do so for we failed to rear them even to the pupal stage.
Searching was more profitable than beating, low-growing plants yield-—
ing rather better at this time of the year. But it remains to be seen
whether the larvae of Zygaena ewulans, found at 9,000 feet, can be suc-
cessfully hibernated at sea level, or whether larvae of Dasychira fasce- ~
lina, found wandering just before hibernation on and near clumps of
alpine rose, will take kiadly to a different foodplant in the spring.
However this may be, it adds greatly to the fascination of a new. and
unknown locality to spend at least a few hours with the beating-tray
at intervals of a week, even if the results are small.
It was not necessary to search for colonies of the larvae of Huvancssa
antiopa, which were easily to be found on the narrow-leaved willows.
that fringe the banks of the Clairé. Of some hundreds of larvae taken |
after the last moult, not one yielded a parasite, yet the chrysalids we
found in odd places produced nothing but hosts of Chalcid flies. The
same result is often obtained by those who have the patience to search
in nature for chrysalids of other Vanessids, such as Ayglais urticae,
Eugonia polychloros, Vanessa io, which are unprotected, but chrysalids
of V’. atalanta, which are concealed in a kind of tent of spun-together
leaves of nettle, rarely produce these parasites. An observation we were
enabled to make seems to prove that the parasite attacks not the larvae
but the newly formed chrysalis, while its skin is still too soft to resist
its attacks.. Two small flies were seen late one evening in attendance
upon a larva of A. urticae that was hanging from the lintel of a way-
side shrine, and the next morning one was observed apparently oviposit-
ing through the soft skin of the newly changed chrysalis, in spite of the
violent twists by means of which this latter was endeavouring to dis-
lodge the larval skin, for the change had but just occurred. Thinking
we could easily find chrysalids of #. antiopa in nature, and so gain some
idea of the percentage that escaped this melancholy fate, we devoted
some time to search around a tall willow bush on which, to judge by
their ravages, at least five hundred larvae must have fed. Yet we could
not find a single chrysalis. Later on a few were found by chance in
various odd situations, but never anywhere near the bush on which the
larvae must have fed. How a large brood scatters so far and hides so
successfully is little short of wonderful.
A LOCALITY IN THE HIGH ALPS. 59
Owing possibly to the abnormally hot and dry summer, the insects
captured showed considerable range of variation, and a few notable
aberrations. Amongst these latter should be recorded a specimen of
Aryynnis niobe, unfortunately badly battered, almost wholly black, with
a single splash of tawny yellow on the upper surface of each wing; an
underside aberration of Plebeius argyrognomon g , in which the mark-
ings are reduced to thin black streaks; an almost completely black
specimen of Nemeophila plantaginis ; a shining white Brenthis pales; a
silvery white aberration of Melitaea didyma, which was not captured ;
and a wonderful aberration of Gnophos serotinavia having the nervures
of the wings powdered with greyish, and the spaces between them filled
in with brownish black.
It may upset our insular notions to elk about immigration in con-
nection with a locality situated on the continent, yet there can be little
doubt that certain species regularly spread each year over higher and
more northerly regions, only to be cut off by the rigours of a normal
winter. In an exceptional season such as has been experienced this
year in south-eastern France, the range of immigrating species is
presumably increased, as well as their numbers, and at the same time
there is much greater likelihood of an unusual partial second brood in
species normally single brooded in any given locality. Only in some_
such way can the presence of some of the insects observed be accounted
for. For example, larvae and imagines of Heliothis peltiyera were
taken ; a few specimens of Leptosia sinapis were taken in mid-August ;
larvae of Hyles euphorbiae were observed of varying size, at altitudes up
to 6,000 feet ; in the valley specimens of Sphina convolvuli were seen,
two of which were found dead, but in perfect.condition, possibly killed
by the night frosts, while another was observed to remain on the same
post for three days and nights; two specimens of Phry«us livornica
were taken by day at flowers on the hottest slope of the valley; a speci-
men of Cyaniris argiolus was taken on September 9th, together with
Limenitis camilla; a few specimens of Melitaea cinwia, all males, were
taken in August; Lampides boeticus appeared-in fair numbers at the
end of August; a single male of Polyommatus (Agriades) thetis was
taken in September; strangest record of all, three specimens of
Huchloé euphenoides were seen in the second week in August,
one female only being captured. Not only among the Lepi-
doptera but in other orders the same phenomenon was observed,
notably in the case of the Orthoptera. For the last few years
only, the valley has been devastated by hordes of grasshoppers, the
reason alleged by the peasants being that the winter mantle of snow
has come to cover the ground before any very sharp frost has been
experienced. The result is that the hibernators have been protected
from the low temperatures of winter, and in the space of three years
the grasshopper has become a serious pest. A well known French
entomologist, Monsieur P. Chrétien,* relates that, during an expedition
into this valley, he laid down his net for a short time to search for
larvae, and found on his return little more than the iron rim left. We
were not able to give much attention to orders other than the Lepi-
doptera, although many pleasant hours were spent observing the habits
_* See L’ Amateur de Papillons, I., 83.
60 THE ENTOMOLOGIS!’S RECORD.
of sand wasps, which provision their cells with lepidopterous larvae, or
watching the graceful flight of that weird, predatory, and ferocious
Neuropteron dAscalaphus italicus, whose captures seemed chiefly to—
consist of Hvebia tyndarus. Of dragonflies only five species
were captured, all in the valley; Symwpetrum scoticum and S..
flaveolum in some numbers, S. striolatum not commonly, deschna
cyanea commonly, and a single specimen of a species of Lestes,
too faded to identify. That Névache is a fine hunting ground for.
the student of any branch of entomology and a paradise for the
botanist we are convinced, and for those who wish to escape for a time
from the exacting duties of life in a large town, no better spot could be
found wherein to pass a few weeks in peaceful seclusion. _
(To be continued.)
TOTES ON COLLECTING, etc.
A Norte on Cronus woopi, Donits.—In the Ent. Mo. Mag. (1924,
LIX., p. 34), Mr. Champion, when discussing the above named species,
described by me in 1921, the types (g and 2) of which are in the
collection of the late Canon T. Wood, writes as follows :—‘ These
insects, in my opinion, are undoubtedly a form of CU. scrophulariae, L.,”’
and further, ‘‘ Cionus woodi, Don., must therefore be treated as a
variety of C. scrophulariae, L.”” Mr. Champion is of course entitled to
his opinion in the matter, but the following points appear to me to call
for some comment.
1. The abbreviation for my name should be Donis., “ Don.’’ has
always stood for Donovan.
2. It would perhaps have been treating me with greater fairness
had mention been made of the fact that before describing these insects
they were first sent to Major Sainte Claire Deville (who declared them
to be quite unknown to him and undoubtedly new) ; and also submitted
to Dr. G. K. Marshall, F.R.S., who makes a special study of the
Curculionidae. The latter gentleman likewise expressed his entire
agreement with the view that the species was new to science, and
kindly helped me to work it out with Wingelmiiller’s table on the genus
Cionus. He also read through and approved of my MS. description.
3. The point, however, which strikes me most of all, is this—the
late Canon Wood’s collection of British Coleoptera has only recently
been presented to the British Museum (Natural History). In that estab-
lishment the Coleopterists are of long standing, merit, and recognised
ability. Yet, almost before the insects in the collection in question can
have been registered and arranged, a third party steps in and decides
what certain insects shall be called, and publishes his views on the
subject ; thus greatly reducing their value. Is the staff of the Museum
incapable of dealing with a collection of beetles placed in their care ?—
Horace DonistHOoRPE.
Tue CannipaL CoccineLuiv.—Those of us who have at any time
bred Coccinellidae know from experience, the reprehensible habits of this
species to cannibalism in their early larval days and Mrs. O. A. Merritt
Hawkes, M.Sc. (Birm.), B.Sc. (Lond.), has given us her experiences of
this painful trait in a racy article in a recent number of “ Conquest”
(August, 1923). I was not however aware till last year that these
NOTES ON COLLECTING. 61
unpleasant habits were continued after reaching years of discretion, or,
in other words, after emergence from the pupa stage. It so happened
however, that in the course of last year on two several occasions I had
placed in separate boxes two Coccinellids( A. 2-punctata, L.), while
still in the yellowish-white dress of emergence, to await the develop-
ment of the elytral markings. By some accident I forgot to attend
to these boxes for some time, and on opening them I found in one case,
one Coccinellid had entirely eaten out his neighbour, leaving only
thorax and elytra picked as clean as if they had been eaten out by ants,
while in the other case, the stronger had attacked and was eating
away the head of the weaker, who, when released, was able to stagger
about till I putit out of its misery. I also observed on two occasions
larvae attacking pupa, so that so far as this species is concerned, it is
prepared to eat its brother Coccinellid at any stage.—G. C. Leman,
F.E.S.
Hairs or Lycra awietaria.—Sluggish habits of Lycia (Biston)
hirtaria, have often been noted. The following may be of interest :—
At West Dulwich on Monday, April 24th, 1922, at 10.80 a.m., a 9
hirtaria was noticed about 5 feet up on the North East side of a lime
tree, the wind was North West and cold, from Tuesday to Saturday it
remained in exactly the samespot. On Sunday, April 30th, at 11 a.m.,
it was noticed to be iz cop. At 6.80 p.m., they were separated, the 9
being in the same spot, the g about 3 inches away. On Monday,
May Ist, at 11.30, the @ was again in cop., the (?) other male being in
the same place 3 inches distant.
On Tuesday the 2 was alone but on Wednesday at 12.30 it was
still at same spot with one male three inches away and 3 other females
a foot or more below it on the South side of the tree. On Thursday,
12.30 noon, the @ was still apparently on the same spot, but on Friday,
May 5th, it had gone.—G. S. Rosertrson (M.D.), 72, Thurlow Park
Road, Dulwich, S.H.
THe Season 1n SoutH Hants.—The terrible sequence of bitterly
cold east winds has not given us much chance to go hunting, but still
we have been out. I have been collecting larvae of Thera variata (I
hope the real variata) from spruce, and 7’. obeliscata (presumably) from
Scot’s pine, but I can find no point of difference in the larvae —in fact,
I cannot be quite sure what I have got. Hylaea (Ellopia) prosapiaria
larvae are very rare this year. Malenydris multistrigaria is well out
and Polyploca flavicornis has been almostabundant. Panolis piniperda
is also out but I am afraid there is no Apocheima hispidaria again this
year. Ve have managed to find a few mines of degeria (Sesia) sphegi-
formis, but they are not common. During the short warm spell of
b.W. winds, quite a lot of insects emerged indoors. I got plenty of
Aegeria culiciformis out (forced), some Asphalia ridens, one Drymonia
chaonia, one Pygaera curtula, two P. piniperda, Hupithecia abbreviata,
Pygaera pigra and Hemerophila abruptaria. 1 wonder what sort of a
season is in store for us. It can hardly be worse than the last one.
So far, I have not seen Brephos parthenias nor heard of it, yet there are
plovers’ eggs about and the woodcock are sitting already.— Wm.
Fassnipen, Southampton. April 4th.
62 THE ENTOMOLOGIST 'S RECORD.
G}URRENT NOTES AND SHORT NOTICES.
Volume V. of Seitz Macrolepidoptera of the World, America Rho-
palocera will be complete in about eight months from now. It will
include about 1,140 pages and 208 plates. The publishers hope that
within a year Volume IX., the Indo-Australian Rhopalocera, and
Volume XIII., the African Rhopalocera, will also be finished. The
parts are issued at the rate of about four per month; so far this year
we have received twenty parts.
We are pleased to find the Annalen Naturhist. Mus. in Wien has
recovered to a large extent its pre-war size and style. The current
issue deals very comprehensively with the Tyrrhenian area of which
the Islands of Corsica and Sardinia are the chief geographical features.
An intensive study of the Coleoptera of the region is the basis of the
investigation, with reference to the fauna of all the varied contiguous
areas, lying between the Alps, Apennines, Sicily, Atlas, Iberian and
Pyrenean Mts., not omitting that of the smaller islands such as Elba.
First there is a systematic account of the Coleoptera of Corsica and
Sardinian, then a statement of the area of distribution and possible
origin of each species, an attempt to explain the absence or scarcity of
widely distributed species of adjoining areas, a consideration of the
probable influence upon the coleoptera of the nature of the land
surface, elevation, etc., and finally the characteristics of the more local
areas In the region such as, elevated areas, wooded mountains, Elba,
etc. In a less intensive degree other orders are dealt with in asimilar
way, the Lepidoptera, the Mollusca, the Fish, the birds, ete. The
consideration of the Gibraltar-bridge, the Adriatic-bridge, the Aegean
area, the shores of the Black Sea, the island of Cyprus as sources of
influence is also included. ‘The writer is Dr. Karl Holdhaus of Wien.
SOCIETIES.
Tue EnromonoeicaL Socimty or Lonpon.
February 6th., 1924,—Vics-Presipents.—The President announced
the Vice-Presidents for the coming year to be Mr. R. W. Lloyd, Dr.
G. A. K. Marshall, C.M.G., F.R.S., and Mr. H. Willoughby-Ellis.
Exections or Fettows.—The following were elected Fellows of the
Society :—Leonard Kastham, M.Sc., Zoology Dept., The University,
Birmingham; G. H. Simpson- Hayward, Icomb Place, Stow-on-the-
Wold, Gloucestershire.
Eixursirs.—Dr. H. A. Cockayne exhibited a pathological aberration
of Pyrameis dejeant from Tosari, Kast Java, in which all the scales
which should be cream coloured were devoid of pigment, very thin, and
rolled up at the tip.
Dr. K. Jordan exhibited specimens of earwigs (Arivenia) which are
found on bats in the Malayan Sub-region. Apparently a case of
symbiosis and not of parasitism as the earwigs appear to feed on the
bats’ excreta, etc.
Lord Rothschild exhibited Teinopalpus aureus, a recently described
species of the genus from Kuangtung, $.H. China.
Mr. E. B. Ashby exhibited a female Leucaspis grandis (Chalcididae)
taken at Digne, July 16th, 1923, and called attention to the habit of
carrying the long black ovipositor curved over the back.
SOCIETIES. 63
Mr. H. Donisthorpe exhibited specimens of the Ant Acanthomyops
fuliyinosus taken in the Isle of Man, the most northern locality for the
Species yet recorded, and showed a map exhibiting the area of
distribution of the species in Great Britain.
Dr. Gahan exhibited the dead larva of a Longicorn beetle which
had lived in the Museum for the last six years. When deposited at
South Kensington, it had presumably existed in a piece of wood which
had been in use for domestic purposes for some 25 years, and thus the
larva had in all probability lived for at least 31 years.
Mr. H. Willoughby-Ellis gave his experience with Longicorn
larvae in confinement and said that he was of opinion that to attain
success in breeding Coleoptera it was necessary to introduce dampness
in sueh a way and in such amount that mould could not be introduced,
and to produce longevity the minimum amount of food should be given
just sufficient without causing death by starvation.
Dr. Gahan exhibited living specimens of a luminous Hlaterid beetle
Pyrophorus punctatissimus from the Argentine, and called attention to
the two sets of light organs in these insects, one of which was only
visible when in flight.
Mr. K. G. Blair considered that the chief function of luminosity in
the Lampyridae, as a whole, was primarily a sexual one in securing the
suitable mating of the species, and probably the same function was
indicated in the Pyrophorus. He agreed that the luminosity might
also be of some service as a warning of inedibility.
Mr. J. H. Durrant exhibited a specimen of 7%nea albicomella from
Torquay, July 17th, 1922, a species new to Britain. Nothing was yet
known of its life-history.
Mr. Willoughby-Ellis exhibited the results of his examination of
three ‘‘ castings ’’ of the owl (Athene noctua) sent to him from Cornwall
by Dr. Cockayne. The remains were exclusively of some eight or ten
species of Coleoptera.
Mr. H. Willoughby-Ellis exhibited specimens of Boletophagus
reticulata (Col.), infested with Acarids, probably a species of Gamasus,
which filled all the depressions in the elytra and suggested that it was
a case of phoresy.
Mr. H. Willoughby-Ellis showed examples of the very rare Coleop-
teron Agabus mellanarius from its only British locality and referred to
a, teratological specimen of which the left posterior leg was extremely
small although the parts were perfect.
Professor E. B. Poulton, F.R.S., exhibited the Longicorn beetle
Chlorophorus (Clytanthus) annularis, which had bred in the wall of a
bamboo waterpot from Burmah.
Professor E. B. Poulton, F.R.S., exhibited some of the actual
specimens of Libythea laius, found congregating perhaps before, or
during, migration, as observed by Mr. C. F. M. Swynnerton in 8S.
Africa.
Professor E. B. Poulton, F.R.S., read the account of an invasion
of ‘‘Siafu” or Driver-Ants at Nairobi, as related by Dr. V. H. L. van
64 THE ENTOMOLOGIST S RECORD.
Someren, and exhibited examples of the species Dorylus nigricans,
sub-sp. burmeisteri var. molesta, identified by Mr. W. C. Crawley.
Professor E. B. Poulton, E.R. §., exhibited the Nymphaline butter-
fly Antanartia hippomene, with a dimorphic larva, one form of which
mimics the orange and black banded larva of a Hypsid moth, Amphi-
callia tigris, and read Dr. van Someren’s series of interesting observa-
tions on the various mimetic associations connected with this butter-
fly, in both the larval and imaginal stages.
Tue Souta Lonpon EnromonoGicaL Socrery.
January 10th, 1924.—Miss Emily Chapman and Miss Laura
Chapman of ‘“ Betula,” Reigate, and Mr. Thos. Greer, of Stewarts-
town, Co. Tyrone, were elected members.
Mr. R. Adkin exhibited a short series of the recently introduced
species Blastobasts lignea and gave a short account of what is known of
it so far.
Mr. Enefer, fasciated stems of sycamore and of narcissus flower
head.
Mr. 8. A. Blenkarn, Me ripe of the species of Coleoptera
mentioned by Mr. H. Main in his paper on Provence read at the last
meeting, including 5 species of Onthophagus and Acanthosinus aedilis.
Mr. H. J. Turner, yellow forms of Pieris napi from Médling near
Vienna, spring form lutescens and summer napaeae form flavescens, the
latter the deeper yellow. He showed a spring form of the Irish yellow
napi which differed distinctly from the Médling spring race; the Irish
bright yellow summer form flava which was very rare was also quite
distinct from the summer flavescens.
Mr. K. G. Blair, for Mr. Hirst, a living Brachinus selopeta (Col.)
from Corsica.
Mr. Rayward, females of Anattis efformata and A. plagiata with
microscopical preparations and pointed out the various differentiating
characters.
Mr. Tonge, for Mr. Baker-Sly, Sphinw ligustri bred from a Cornish
larva with the pink marking replaced by cream, and a male Sterrha
sacraria taken at Lewes on August 11th last.
Mr. N. D. Riley, a var. salmacis of Plebeius (Aricia) medon from
Castle Eden Dene, a locality which will soon be utterly destroyed by
the making of roads and railway and by mining operations.
Notes were read from Mr. G. T. Porritt, (1) Scarcity of Lepidoptera,
particularly Tortrices near Huddersfield. (2) A peculiar habit of
Satyrus semele to settle on a scrap of newspaper at St. Anne’s on Sea.
Reports of the Field Meetings at Ashtead and Ranmore Common
were read.
January 24th, 1924.—The Annual Meeting. On this occasion the
reports of the Council and Treasurer were read and passed, and the
President, Mr. N. D. Riley, F.Z.S., F.H.S., read his Address. Subse-
quently Mr. Jacobs exhibited a remarkable, small, very pale coloured
and practically markingless example of Hybernia marginaria taken last
year, and Mr. Blenkarn exhibited a dwarf Huchloris pustulata (bajularta)
taken years ago at the New Forest, of only half the usual expanse.
Subscriptions for Vol. XXXVI. (10 shillings) should be sent to
Mr. Herbert E. Page, ‘‘ Bertrose,’’ Gellatly Road, New Gross,
S.E.14 [This subscription includes all numbers published from
January 15th to December 15th, 1924.)
Non-receipt or errors in the sending of Subscribers’ magazines should be
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Larval habits of Teichobia verhuellella, Stain., Alfred Sich, F.E.S. .. ies ee Se ae iB
Myrmecophilous Notes for 1923, H. Donisthorpe, F.Z.8., F.E.S, nie 69
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LARVAL HABITS OF TEICHOBIA VERHUELLELLA. 65
Larval hiabits of Teichobia- verhuellella, Stainton.
By ALFRED SICH, F.E.S.
My first acquaintance with this species was made at Niton, near
Ventnor, in the Isle of Wight, where I found the larvae on Harts-
tongue Fern, and subsequently bred several moths, but I did not then
notice the interesting habits of the larva, which actually moves its
dwelling from old pastures to new like a nomad. In 19231 again met
with the larvae in plenty at Badenweiler, in the Black Forest, where I
spent the winter, and was pleased to find them again on the Burgen-
stock, a mountain near Lucerne. Here they were living in an even
more natural state than at Badenweiler, as they inhabited limestone
rocks instead of stone walls made by man.
Teichobia verhuellella, Stainton, is on the whole a somewhat primi-
tive species with an ill-developed tongue, two-jointed maxillary palpi,
all veins present and separate, and unicolorous wings, while the larva
mines in an aneient type of plant.* Rebel, in Staudinger and Rebel’s
Catalogue, 1901, places it in a subfamily by itself, the Teichobiinae, and
it appears to have no very near relations. It appears to be distributed
over Central and Western Europe, and I believe it has been recorded
from the United States of America. Near Ventnor it occurred at a few
feet above sea level, on the Burgenstock at 3,000 feet, and Zeller found
it at Bergiin, in the Engadine, at over 4,000 feet. The larva mines in
the fronds of certain species of fern in its earliest stages, and later lives
under a cover of silk and fern spores. I will begin my observations on
the larvae I found at Burgenstock. On August 28th, 1923, the first
mine was seen, but I could find no trace of the egg on this one, nor on
any of those found subsequently.
The first mine is a blotch mine, more or less triangular in outline,
quite flat, and pale brown in colour. The larva has a pale ochreous
head and a pale greyish ochreous body, but my lens would not show me
more of this creature, some 05mm. in length. It lives entirely in the
mine, eating out the green tissue. Here I believe it undergoes its first
change of skin, and then continues to feed for a time in the same mine.
Whether in the first stage it can leave the mine and form a new one I
do not know, but it certainly is able to do so in the second stage. These
mines were in Aspleniwn ruta-muraria. On September 8rd I found a
larva in the second stage on a leaflet of afrond of Asplenium viride. It
had just mined out sufficient space to enclose its body. Above, on the
opposite side of the stalk, was the leaflet containing the first mine which
the larva had vacated. ‘'lhree days later I left Burgenstock, and was
unable to make any further observations. As the leaflets of these
Asplenium ferns are often very small, I should suppose that the larva
makes two mines at least before hibernation. It may, however, be
content with one mine when feeding in the large fronds of Hart’s-
tongue. Whether the larva passes the winter in the mine, as I think
probable, or whether it leaves the mine and hides away till the spring,
is a problem | have not yet solved. I will now go back to my obser-
vations at Badenweiler, in the spring of 1923. There was a fair amount
* Compare Meyrick, Handbook, p. 777.
May 15ru, 1924.
66 THE ENTOMOLOGIST’S RECORD.
of A. ruta-muraria on the walls of the villages in the neighbourhood,
and I intended looking out for the larvae in April, as Tutt gives that
month for finding it in England (Practical Hints, Vol. III.), and as
Badenweiler is about 1,200 feet above the sea, I thought the species
would not be earlier there. However, happening to be in the village
of Niederweiler, on February 26th, I saw a good patch of the fern,
and, on examination, I was surprised to find several larvae under their
covers, all in the last stadium. From time to time others were found
in various places, some on Hart’s-tongue, which was not very common
in the district, anda few on Asplenium trichomanes, which was abundant
but is, I fancy, a less suitable food-plant than the other species above
mentioned. It was not till March 22nd that I was able to find any
larvae in the penultimate stage. These occurred on the highest and
most exposed position that I searched, and on 4. trichomanes. They
had already left the mines and were living under their covers just like
those in the last stage. In these two last stages the larvae live on the
underside of the fronds, not in a case as some authors state, but under
a tent or cover made of the spore capsules of the fern. It may not be
wrong to call the dwelling a case, but I prefer the word cover, as it is
entirely different from the cases of Coleophorids, Psychids, or Adelids.
When examining the fern I first noticed, the pale patches on the upper-
side of the leaflets where the larvae had been mining. On turning over
the fronds I saw the covers spun on to the underside of the leaflets.
They are formed of the spore cases of the fern and silk enough to hold
them together, so that they are exactly the same colour as the groups
of spores, and but for their size and irregular position they might be
readily passed over. When on Aspleniiun, where the leaflets are small,
the covers usually are spun across two leaflets, so that they are easily
seen. The shape of the cover may be likened to that of a rowing boat
in reversed position, but without a keel. At rest the larva is very
plump and the cover appears to house it conveniently. The edges of
the cover are fastened to the fern, but there is an opening at each end.
With its body hidden under the cover, the larva bites through the lower
cuticle of the leaf and mines patches out of the interior. It places its
excrement outside the cover at the more exposed end. When the fronds
in the tin box, where I kept the larvae, began to get dry, I put fresh
- ones in and took the larvae out of their covers, placing them on the
fresh fronds. They soon began to form new covers by biting off the
spore cases and spinning them over their bodies. One was quite hidden
in three hours, while another was still half exposed at the end of that
time. In my walks I frequently found the covers, and began to notice
that these often occurred on leaflets where the spore groups had not
been disturbed. This puzzled me, as I was still under the impression
that when a larva moved to a fresh leaflet it there formed a fresh eover.
I did not then know that it usually took its cover with it when it moved.
Finding that the fern dried up rather quickly in the tin box, I gathered
some fronds with long stalks and placed them in a small glass tube
with a little water at the bottom, and as the larvae were sluggish no
cork was needed. Here they did very well, and I could observe them
without disturbance. One evening on looking at them I noticed two
larvae crawling down the stalk of a frond and underneath each was a
flat piece of their covers. The progress was slow, and in the failing
LARVAL HABITS OF TEICHOBIA VERHUELLELLA 67
light I could not make out how the cover was carried and kept in posi-
tion just below the larva. I thought that perhaps the larva had spun
the cover to its body, but I induced one larva to crawl beyond its cover,
and finally it fell into its cover. I then saw the cover was fastened to
the stalk. The cover when carried by the larva is rather flat, more or
less quadrilateral in shape, and rather stiff by reason of its silk lining.
So far as I could see, the larva after spinning one corner of the cover
to the stalk, seized the opposite corner in its strong jaws, pushed it
forwards and fastened it. Then cutting loose the first corner moved
that forward again. In this manner slow progress was made. The
larva is strong for its size. Unfortunately I never saw the larvae on
the move in a good light. On one occasion I placed a larva and its
cover on a fresh frond, but the cover fell a short distance away from
the larva. Being in a hurry I left it where it fell. When I looked
again I found the larva had fetched its cover and spun it on to the fern
in another place. When on the growing fern I do not suppose the
larva moves frequently, as it is quite a small one when fully grown,
and not of an active nature. When about to spin up, it either crawls
down among the fern stalks or finds its way on to the wall or rock, as
the case may be, and of course carries its cover with it, as this is made
use of for the cocoon. In the open I have found one cocoon on the
stone of a wall and two on the stalks of fern. Of those I had in
captivity four spun up on the fern and two on the glass tube. The
cocoon is firmly attached and has more silk on the floor than the cover.
It retains the same colour and shape, but may be recognised by a ridge,
which runs along the top. Its colour is light brown, its length about
7mm., and its width about 2mm. ‘The larva lines the sides of the
cocoon thiekly with whitish silk, nearly up to the ridge. Thus, at the
top of the rather stiff sides, there is a strip of loose material, which
gets pinched up to form the ridge. My larvae spun up during the first
fortnight in April, except one, which must have done so earlier, as the
moth appeared on April 26th. This was abnormally early. The last
one bred appeared on June 9th, and June and July are given as the
usual months when the moth is on the wing. When the moth is about
to emerge the pupal shell is thrust out of the cocoon as far as the third
abdominal segment. I have not found the moth in the open, but those
I have bred never showed any activity.
The full-grown larva is pale ochreous, short and stout when at rest,
but when feeding the anterior segments are stretched out and become
much flattened. Head black, clypeus marked out with yellow, pro-
thoracic shield black with pale anterior collar, and divided by a yellow
suture. Legs short, black. Four pairs of abdominal prolegs with
complete ring of crotchets. The claspers havea horse-shoe of crotchets.
There is a black anal shield. Length at rest about 5-6mm. On the
meso- and meta-thorax tubercles i and li are on a common plate. On
the first and second abdominal segments the pair of tubercles i are
closer together than the pair of ii, as in most lepidopterous larvae. On
the third abdominal the pairs are of equal distance apart, but on the
fourth and subsequent segments tubercles 1 are wider apart than
tubercles ii. This arrangement is not uncommon in some of the
Tineina. The larva in the penultimate instar has the head deep olive
brown, without yellow marks, and the prothoracic shield olive brown,
68 THE ENTOMOLOGIST S RECORD.
very faintly divided by a paler line. Otherwise the larva resembles
that of the final instar. Length about 3mm.
The pupa, about 4mm. long, is light ochreous and rather stout. In
the ¢ the abdominal segments 8,4, 5,6 and 7 are free. The antennae,
wings, and third pair of legs come down as far as the 7th abdominal.
The prothorax is about double the size of the dorsal headpiece, show-
ing that the pupa does not belone to the Adelid-Tineid series. The
tongue is very short, maxillary palpi very conspicuous below the eyes.
Some of the abdominal segments appear to have the upper row of dorsal
teeth. On the dorsum of the ninth abdominal there is a pair of strong
spines, slightly curved upwards, which probably help to hold the lower
part of the pupal shell in the cocoon while the moth is emerging from
the upper exposed portion. I could not with my lens make out any
setae.
From the foregoing it may be gathered that the larva is purely a
leaf-miner and does not eat the fructification of the fern, that it has
four instars and hibernates in the second. I believe now that it leaves
the mine before winter.
Of the food-plants Phyllitis scolopendrium is no doubt useful. Its
large fronds provide ample mining space. A possible disadvantage
may arise from its flat leaves offering little means of concealment. The
larval cover is usually placed either between the long rows of spores or
adjoining one of them. The larval mine is fairly conspicuous on the
green upperside of the frond. The common Wall Rue, Asplentum ruta-
muraria, especially where it grows in thick tufts, is a convenient food-
plant. The leaflets are sufficiently thick and sappy to afford good
mining material, and the numerous fronds provide shelter for the larval
covers, the cocoon, and the perfect insect. The fronds mostly remain
green throughout the winter, except where they are exposed to severe |
frost; by June and July the young fronds are of sufficient size to
accommodate a small mining larva. These plants sometimes grow on
old walls in towns, but then are usually so covered with the webs of
spiders as to be unsuitable to moths. Besides 7. verhuellella I have
found, not uncommonly, a yellow dipterous larva mining the leaves.
One I bred was a slender gnat-like insect. Asplentwn trichomanes is
also an abundant fern in the limestone districts of Germany and
Switzerland, and it often grows in fairly thick tufts. The leaflets are
thin and rather dry, and do not appear to be so suitable for a mining
larva as the leaves of the wall rue. The moth seems to prefer the
latter plant for oviposition. Asplenium viride is a more local species
and prefers higher elevations. The leaflets are also small, but they
contain more sap than those of A. trichomanes. It is a delicate plant,
and many of the fronds wither during the winter. Ceterach officinarum
is quoted as a food-plant. It is rather a local species, but it looks
suitable, though the mine would be conspicuous on the even green
upperside of the frond. I should much like to find the larva on this
in order to see if it used the scales, which thickly cover the underside
of the fronds, in forming its habitation.
Bruand stated that the larva fed on “ capillaire.”’ This word seems
to have puzzled the entomologists of the Staintonian period, but
according to Frey it is a collective term for the species of the genus
Asplenium.
MYRMECOPHILOUS NOTES FOR 1923. 69
Myrmecophilous Notes for 1923.
By H. DONISTHORPH, I.Z.S., F-H.S.
(Concluded from page 53.)
CoLEOPTERA.
The following species were taken with ants in Dean Forest in June,
all of which were new county records:—Oxvypoda haemorrhoa, Sahl.,
with 4. (C.) flavus and Ff. rufa; O. formiceticola, Mark., Thiasophila
angulata, Er., and Notothecta flavipes, Gr., with I’. rufa.
Drusilla canaliculata, F.—This beetle, and two of its larvae, were
found in a nest of A. (D.) niyer, under a stone at Dever, on May Ist.
I have found the larvae of Drusilla on several occasions in ants’ nests
ere this, and I recorded such an occurrence in the nest of Myrmica
ruginodis, at Nethy Bridge, on July 20th, 1913 [ Hnt. Rec. 26, 42 (19) 4)].
My friend Mr. Keys, has also sent me this larva to name, which he
had taken with ants at Plymouth. It is very like the perfect insect in
appearance, though of course only superficially.
Mons. R. Stumper suggests that this beetle is only an accidental
ant-guest, and he considers that further observations and experiments
are necessary to settle the question [| biol. Centralb., 85, 189 (1920)].
He is evidently unaware of the very numerous records of its occurrence
with ants, and also of my experiments with the beetle. It would take
up far too much space to give anything like a full st of all such records
extant; but the following may be mentioned to demonstrate the points
in question.
In 1887 Aubé records it with ants in France (Ann. Soc. Ent.
France, 1887, 458-69), in 1843, F. Smith recorded it with A. (C.) flavus
at Mickleham in Surrey (Zool. 1843, 268); in 1844 Markel gives
several species of ants as its hosts [Germar, 5, 198-271 (1844))| ; in
1848 Bold says it tenants the nests of ants and preys on the inhabitants
[Cat. Col. North and Durh., 1384 (1848)|. The italics are mine; Bold
was a first rate observer, and this is as far as I know the first record of
the beetle feeding on ants. Many field observations, such as the
Phoresy of Antherophayns, ete., were first published by him. In 1876,
Lucante and Bleuse record that they saw a Drusilla “run after an ant,
which not having time to escape, was seized and carried off.” = [ /nt.
Mo. Mag. 18, 65, (1876)]. In 1890 Wasmann says it occurs commonly
with M. laevinodis, M. ruginodis and M. rugulosa {[Tijd. v. Kntom. 38,
69 (1890)}. On May 38rd, 1898, Wasmann found at Linz a Drusilla
running on a path in a field with a dead Myrmica in its mouth (Deuts.
Ent. Zeit., 1894, 274). On July 17th [not June}, 1900, Donisthorpe
captured a Drusilla which was running in the porch of a cottage at
Chiddingfold with a dead ant [Myrmica] in its jaws. This he said
helped to show of what the food of the beetle consisted, and why it
occurred with ants [Hnt. Rec., 42, 238 (1900)|. In 1901 Donisthorpe
brought up from Portland a number of this beetle taken in nests of
A. (C.) flavus and A. (D.) niger, and on April 28rd, he introduced
several into his large J’. xwfa observation nest. The beetles ran about,
and entered the nest, appearing to avoid the ants by their quickness,
and hiding under twigs, etc. When two rufa % 8 were placed in a
small box with several of these beetles, the latter’s defence proved to be
the same as in Dinarda, Myrmedonia, ete. (i.e., by thrusting the tail
70 THE ENTOMOLOGIST S RECORD.
into the ant’s face, and giving off the ‘“‘ Myrmedonia odour”). They
were left with the ants in the small box all day, and none of the
beetles were injured. When however arufa 8 was forced to seize a
Drusilla, it did not let go as with Mymedonia, but dragged the beetle
into the nest. On June 80th, a Drusilla was seen to come out of the
nest, and run quickly about, hiding itself among the pine needles.
This beetle therefore had lived in the rufa nest for nearly three months
[Ent. Rec., 18, 851 (1901)|). On May 80th, 1906, Walker captured at
Cumnor Hill, near Oxford, a Drusilla carrying a niger % in its jaws.
In 1909 Donisthorpe in a paper on the “ Origin and Ancestral form
of Myrmecophilous Coleoptera,” after recapitulating some of the above
facts, remarks that the defence of Drusilla was evidently not so perfectly
developed as in Myrmedonia ; and that as the glands which secrete the
odour given off became better developed, the beetle would be able to
inhabit the nests of ants with greater impunity, and eradually become
a more regular guest. No doubt some such steps as these have taken
place with the Myrmedonias (Zrans. Hut. Soc. Lond., 1909, 404).
On July 21st, 1910, Donisthorpe found a Drusilla at Hanwell
carrying off a freshly killed niyer ¥ ; and on September 6th, of the
same year he took another at Ditchling with a dead MV. scabrinodis 3
in its jaws [/vnt. Rec., 28, 60 (1911)}. Again on May 18th, 1913,
Donisthorpe captured at Bletchington a Drusilla with a half dead J.
scabrinodis % in its Jaws [Mnt. lec., 26, 42 (1914)].
I may mention that I have taken this beetle in the nests of the
following species of ants in Britain:—Ponera coarctata, Myrmica
laevinodis, M. sulcinodis, M. ruginodis, M. scabrinodis, Leptothorawx
acervorum, Letramoriun caespitium, A. (D.) fuliginosus, A. (1).) niger, A.
(D.) alienus, A. (C.) flavus, f°. rufa, In, ewsecta, F. sanguinea, F. fusca,
and HH’. fusca var. glebaria.
It is evidently quite clear that Drusilla canaliculata may be classed
as a “hostile persecuted lodger’’ (Synechthran) ; its food consisting of
ants and its larvae cccurring in the nests as is the case with most of
the Myrmedonias. Its defence is not yet as perfect as in Myrmedonia,
and it has probably not been so long a dweller with ants.
DirrTsra.
Aptochaeta ciliata, Zett.—A specimen was taken with 4. (D.) brunneus
at Theale, on February 6th. I have previously taken it with A. (D.)
fuliyinosus in plenty at Wellington College, in 1906, and at Darenth
Wood in 1910.
Limosina crassimana, Hal.—l took a specimen of this fly with A.
(D.) brunneus at Theale on June 20th, some of the species of Limosina
evidently show a tendency to inhabit ants’ nests. 1. curtiventris was
taken with 4, (D.) fulivinosus at Woking on May 26th, this year, and
in the same nest in May and July 1920. It occurred with the same
ant at Darenth Wood in September, and I bred it in plenty ina
fuliyinosus nest trom Wellington College in 1906. I have taken L.
rufilabris with I’. fusca, and LL. fungicola, and Limosina sp. with
fuliyinosus. I am indebted to Mr. Collin for the names of the above
species of Diptera.
Phyllomyza.—In ** Konowia”’ in 1923 [2, 44-7 (1923)|, Schmity
published a table of the European species of Phyllomyza, and described
MYRMECOPHILOUS NOTES FOR 1923, Wal
three new species, two of which, P. formicae and P. donisthorpet, are
myrmecophilous.
P, formicae, Schmitz.—This is the species I have been recording
for years from Pormica rufa nests sub P. formicae, Collin MS. It was
originally brought forward as British by the late Mr. Verrall in his
second hundred new British species of Diptera, sub P. secwricornis, Fin.
[Ent. Mo. Magy. 30, 146 (189+)], on specimens swept by himself over
nests of the wood ant [=F rufa] at Braemar, on July 25th, 1873.
He pointed out that his specimens had darker legs than continental
types and descriptions, but that he was not well acquainted with the
group. It was not taken again until 1901, when I discovered it at
Oxshott in rufa nests. I have also taken it with the same ant at
Weybridge and Nethy Bridge; and have bred it in my large rufa
observation nests from the two former localities. I bred it from larvae
which I brought back from rufa nests at the last named locality.
P. donisthorpet, Schmitz.—This species, which I have recorded as
Phyllomyza sp. from fuliginosus nests, was first taken by me in a nest
of that ant on the Birkdale sandhills on June 22nd, 1905. I sub-
sequently found it at Wellington College, Darenth Wood and Oxshott.
Schmitz records a specimen (?) sent to him by the British Museum,
as having been taken in a rufa nest at Weybridge. This of course was
given by me to the British Museum, and I cannot help thinking that
either the Museum, or I, had mixed the data of the specimens up in
some way, and that it was really taken with fulivinosus.
P. lasiae, Colun MS.—Unfortunately none of the $ g of this fly
sent to Father Schmitz by the Museum and myself were in good enough
condition to be described. It was first taken by me at Oxshott, on
April 26th, 1901, in a fwliginosus nest, and I subsequently found it in
numbers with the same ant at Wellineton College and Woking. Ihave
also bred it from larvae and pupae taken in the two latter localities.
Microdon egyert, Mik.—On May 14th Mr. Edwards kindly gave me
two puparia of this species from Woking. I placed them in a chamber
of one of my observation nests, and one hatched on May 21st, the
second on May 26th.
According to Edwards all the specimens of M. latifrons, Liw., both
adults and puparia, in British collections, are really M. eggeri, Mik.
[Hint. Mo, Mag., 59, 233 (1923)|. His reasons for this statement
appear to be quite sound, and he mentions most of the British records.
He appears to have forgotten, however, that the late Dr. Sharp brought
M. eggeri forward as a British insect on the strength of a specimen
captured by himself at Rannoch, early in June, 1910. [Mnt. Wo. Maqg.,
46, 274 (1910)]. Sharp mentioned that Wasmann had taken the
species in Luxemburg, but he (Sharp) could not remember the refer-
ence. I pointed out that Wasmann published his notes on this species
in the Archiv. trimestr. d. UInstit. R. Grand-Dukal, Luvemburg, 1909,
T.IV., Fascic. I11., p. 50, and that the host was Formica sanguinea; etc.
[Ent. Mo. Mag., 47,43 (1911)].
The occurrence of this species in Britain would appear to be as
follows :—
’
THE ENTOMOLOGIST S RECORD.
Loca.iry. DatE Capror. PHASE. Host. REFERENCE,
1. Oxshott es ee ae 3 3 Grant. e Adult. Ree | Verrall, Brit. Flies, 8, 1901.
2. Sore : ie Be ee Unknown. Proc. Ent. Soc. Lond., 1900, xiv.
3. New Forest stag rhe 1902. ae i Ee Eas ray Mo. ae 38, 206 Bete
ee : ; June, 1910. Bis a Adult Unknown. Ent. Mo. oe 46, 274 (1910).
5. Wimborne... 1911. iss Seca eae Unknown. Ent. Mo. Mag., 59, 233 (1923).
6. Woking Fy ee Scan Puparia. Tee. ee ean feos nt. Mo
( Ascot. = ean es - giftinand ao nes oe Heo Bate:
8. New Forest .. | May ab & 11th, 1922. ee ae . a (D.) ee Ent. ce 35, 7 (1923).
- eee : ae ae fe aoe : Ree Puparia. A. (D.) ie FF ee ie Foy
and No. 8, sub M. rhenanus,
?
ert
Nos. 4, 5, and 9, sub M. eg
and M. latifrons ?
.
b)
Mos. 1, 8, 6, and 7 were recorded sub M. latifrons; No. 2, sub M.
devius
MYRMECOPHILOUS NOTES FOR 1923. 73
The host of this species in Britain is, as far as is known at present,
A. (D.) niger. It is almost certain that No. 6, and probable that Nos.
5 and 7, were also taken with this ant.
Peyerimhoffia subterranea, Schmt.—I am indebted to Mr. Edwards
for the name of this apterous Dipteron, a specimen of which was taken
in a nest of f. fusca, at Box Hill, on May 4th. As I have taken
another species of this genus in ants’ nests (/.¢., P. brachyptera, Kieft.,
with A. (D.) alienus, on Lundy Island, in June, 1913 [Hut. Rec.. 25,
268 (1913)], it would appear that they really have something to do
with ants. A small soft-bodied apterous “ fly’ would not otherwise
seem to have much chance of survival in an ants’ nest !
APHIDAL,
Trama radicis, Kalt.,and Gevica formicina, Buckt., occurred in some
numbers in nests of A. (D.) niyer, under stones, at Dover, on May Ist.
Forda formicaria, C. Heyd., and Geotca carnosa, Buckt., were found
together in a nest of 4. (C.) flavus, in Dean Forest, on June 138th.
Stomaphis quercus, L.—On June 18th I observed a number of .8 $
of A. (D.) fuliginosus walking in files along a fence, in a ditch, and on
two large oak trees, at the far end of Wimbledon Common. Some of
the ants were noticed clustering round something on several places on
the bark of one of the oak trees. Closer inspection proved that they
were attending individuals of this curious aphid, which had their very
long proboscis inserted into the bark of the tree. It will be remembered
that I found this same aphid, attended by the same ant, at Woking,
on September 22nd and October 7th, 1921 [Hnt. Nec., 34, 21 (1922)].
Forel, in Vol. II., p. 118, of his Le Monde Social des Fourmis, 1922,
shows that this plant-louse is the usual species attended by Ad. (D.)
brunneus.
Coccrar,
Ripersia subterranea, Newst., was found in nests of A. (D.) niger, at
Dover, on May Ist; and Newsteadia floccosa, de G., with I. rufa, in
Dean Forest, on June 16th.
ARANEINA.
Thyreosthenius biovata, Camb., occurred commonly in the nests of
F’. rufa, in Dean Forest, in June.
Harpactes hombergi, Sep.—An example of this spider was found
with A. (D.) brunneus at Theale on February 6th. I believe this is not
regarded as a myrmecophilous spider especially by those who only
study these arthropods. Nevertheless, however, it is frequently found
in company with ants, upon which it feeds, and may be regarded as a
synechthran. The late O. Pickard Cambridge wrote—“It will not
easily be mistaken for any other species on account of its linear form
and creeping ant-like movenents’’ [Brit. Nat., 1, 65 (1891)|}. The
italics are mine. In my notes on Myrmecophilous spiders in 1908,
I considered it belonged to my group II.—‘“ Those species which hunt,
and prey on ants. They are generally found outside and in the neigh-
bourhood of the nests.” [Zool., 1908, 420]. I have constantly met
with it in ants’ nests; especially with A. (D.) fuliginosus, with which
species Wasmann records it on the Continent.
74 THE ENTOMOLOGIST S RECORD.
CoLLEMBOLA.
Cyphodeirus albinos, Nic—This little creature was abundant in nests
of A. (C.) flavus, at Colby Glen, Isle of Man, on September 19th; its
first record for this island. This is another instance of an insect, which
could hardly have reached the island except by crossing on dry land.
CRUSTACEA.
Platyarthrushoffmanseggti, Brdt.—This little myrmecophilous wood-
louse was abundant in nests of A. (C.) flavus at Colby Glen, 1. of Man, on
September 19th, its first record for the Isleof Man. Dr. Scharff writes
as follows concerning the distribution of this species—‘‘I have had
occasion to mention once before an extremely interesting genus of
Blind Woodlouse, viz., Platyarthrus. Like Testacella it lives under-
ground, and also resembles it in its general range. It is difficult to
conceive that Platyarthrus, from its peculiar mode of life, could have
crossed any formidable barrier, such as even a narrow strait of sea.
Its occurrence in Spain and North Africa indicates, therefore, that the
straits of Gibraltar did not exist at the time when it undertook the
migration southward, just as the English Channel and the Irish Sea
could not have been there when it wandered to England and Ireland.
The species which occurs in the South of England, has a wide~range
in Ireland, and reaches in Scotland its most northern Kuropean limit
of distribution, Platyarthrus is only one of the Lusitanian genera of
woodlice . . . . “If the presence of Platyarthrus in North-west
Africa proves that the Straits of Gibraltar had come into existence after
its southward migration, it also suggests that the ancestral home of the
Woodlouse was in the Spanish Peninsula. Whether this supposition
is correct or not, does not affect the Straits of Gibraltar problem, for
in a migration northward into Spain from Morocco land-connection
would be equally necessary. Almost every group of vertebrates, and
invertebrates furnishes instances of species which must haye crossed
the Straits on dry land.” (Vhe History of the European Fauna, London,
1899, pp. 299-3802.) These same arguments support what I have
written above in connection with the presence of dA. (D.) fuliginosus
on the Isle of Man, and help to show that the Island was connected
with Ireland or England after the disappearance of the iee.
A word about the British distribution of Platyarthrus:—It is not
confined to the South of England, but is now known to occur in the
Midlands, Yorkshire, Lancashire Mid., and Durham; it is found in
the Isle of Wight and extends from Hampshire to Durham, without a
break. In Scotland it appears to be very rare, I have never taken it
there, and I have records only from Fife and Kinross, and Banff. In
Ireland I know of its occurrence only in the South, and South-Hast,
but no further north than Dublin County.
Lacerrinia.
Anguts fragilis, L.—On June 18th, a slow-worm was found in a
nest of Hormica fusca in Dean Forest. The ants’ colony, which was a
large one, was situated under a large flat stone, and the slow- worm was
resting coiled up in the midst of the ants. It glided away into the
grass by the side of the nest when the stone was lifted. I have on
several occasions in past years found slow-worms in ants’ nests, at
RECORDS OF LEPIDOPTERA FROM’ SURREY. 75
Weybridge and elsewhere. In 1902 I mentioned that the late A. J.
Chitty frequently found slow-worms in nests of . fusca at Dorington
in Kent, and said that this was worth recording as the Amphisbaena, a
blind, snake-like lizard lives in the nests of the leaf-cutting ants on the
Amazons. In Guiana, a legless lizard, Caecilia annulosa, also lives in
the nests of the fungus-growing ants [Hnt. Rec., 14, 15 (1902)|}. Mr.
J. Clark informs me that there are several species of snakes living with
ants in Australia.
Further Records of Lepidoptera from the Witley District of Surrey.
By W. HAWKER-SMITH, F.E.S.
Since the publication of Mr. Tullett’s ‘‘ Notes and Observations on
the Lepidoptera of the Witley District, 1912-1919,” in the H’ntomolo-
yist’s Record, Vol. XXXII., nos. 8, 5, 6, the following notes and records
of additions to the List have come to hand. For these we are princi-
pally indebted to Messrs. H. T. G. Watkins and J. HE. Eastwood, who
kindly furnished us with lists of captures made in the district, either
by the latter or by Mr. E. G. R. Waters, and which are not recorded
in Mr. Tullett’s paper.
But first of all I must dispel the illusive report of Sérymon prune
and explain how it came to be recorded. We have lately discovered
letters showing that some pupae of S. pruni had been purchased from
a dealer in the same month and year in which the larvae were recorded
to have been beaten, and it is clear that some of the purchased pupae
(from Huntingdonshire) became accidentally mixed up with pupae of
Rurales betulae from larvae beaten in May, 1919, and, emerging at the
same time, were supposed to have been among the beaten larvae.
The List published by Mr. Tullett is a fairly long one considering
the fact that the Pyrales, Tortrices and Tineae are omitted ; so itis not
surprising that few names have been added to the list in the four years
since 1919, and that most of the following are records of species taken
in this district by other collectors previously to the time covered by Mr.
Tullett’s paper.
Papinionipar.—Sub-family Pierinae.—Colias hyale, L. Hastwood
records one at Hinton in 1892.
NympuHatipar.—Sub-family Nymphalinae.—-Euvanessa antiopa, L. Two
taken at ivy bloom, at King Edward’s School, about 1870, by a
gardener, were seen by Hastwood.
Argynnis aglaia, L. One, below Hambledon Common, recorded by
Hastwood.
Melitaea aurinia, Rott. _One in the Hill Museum, taken 3.V1.1914,
Witley.
Lycanniwar.—Sub-family Lycaeninae.—Strymon w-album, Knoch. This
species is recorded from Witley in Newman’s British Butterflies.
He lived at Godalming.
Polyommatus (Aricta) medon, Hufn. Recorded for Witley in plenty by
Hastwood.
Polyommatus (Agriades) coridon, Poda. Waters records one on Witley
Common (Rodborough), 1905; also several in a meadow at
Chiddingfold, apparently freshly emerged, 1911.
76 THK ENTOMOLOGIST’S RECORD.
Spxineipan.—Manduca (Acherontia) atropos, L. One, at Sweetwater.
At rest in afternoon on grass, recorded by Kastwood.
Mimas (Dilina) tiliae, L. Recorded at Witley from pupa dug under
elm. (Hastwood.)
Ayrius (Protoparce) convolvuli, L. Witley. Kastwood notes this as very
plentiful in 1891.
Humorpha (Chaerocampa) elpenor, L. Recorded from Witley by Hast-
wood.
Theretra (Metopsilus) porcellus, li. Also recorded from Witley by
Eastwood.
Noroponripan.—Drymonia chaonia, Hb. Witley (Mastwood),.
Phaeosia dictaeoides, Esp. Watley (Kastwood).
Notodonta ziczac, L. Witley (Mastwood).
Odontosia carmelita, Hsp. Recorded from Witley Common, April 10th,
1912, by Waters.
Palimpsestis (Cymatophora) fluctuosa, Hb. Witley. One at sugar
(Hastwood),
Enpromipar.— Endromis versicolora, Li. Mr. Eastwood’s own note as
regards this species is, ‘‘ No—but I am fairly certain I saw a
male flying on the Heath between Enton and the railway.”
Arctipan.—Sub-family Arctiinae.—Parasenia plantaginis, L. Witley
(Hastwood).
Arctiupar.—Sub-family Lithosiinae.—Lithosia deplana, Esp. Witley
Common, 1914 (Waters), also Hydon Ball.
Nocruiwar.—Sub-family 163
With the help of an assistant acting as a screen between the sun
and the ant, Dr. Santschi placed himself slightly behind or at the side
of the ant and projected on it, from time to time, the rays of the sun
by means of a large mirror (40 x 60 cm.), holding it as still as possible.
The result was that the insect often diverged from its course for a
considerable time, at an angle corresponding fairly exactly to that of
the apparent displacement of the sun. For instance, when the sun
was at the ant’s right, and he displaced it by means of the mirror to
its left, 180 degrees, the insect turned through 180 degrees and pro-
ceeded in an exactly contrary direction to its original course. In short,
when the sun was on the ant’s right and was displaced to any other
position, the ant turned so as to still have the sun on its right.
It must be admitted that this experiment does not always succeed,
a high wind, the presence of a large object close by, the too close
proximity of the nest, or a mirror too small, being sufficient to nullify
it. However, other methods of orientation being excluded, the use of
the sun asa guide is readily demonstrated. Similar results are obtained
by the experiment known as Brun’s “temporary fixation,” which
consists in placing an opaque box over the ant and removing it after
the sun has reached another position. Given conditions similar to the
above, the ant continues on its way to the nest in virtual orientation,
i.e., on a line that takes it away from the nest at an angle equal to
that of the sun’s displacement.
The moon also can serve as a guide in sidereal orientation. This
is illustrated by an experiment as follows. On a moonlight night a
fig on which numbers of Monomoriwm salomonis var. didonis were
feeding was carried some distance away, to ground unknown to the
ants that were still clinging to the fig, and replaced on the soil.
A number of the ants, disturbed by the operation, at once left the
fig and proceeded northwards in correct virtual orientation. They
were walking each on its own, some distance apart, but in parallel
lines. Suddenly they scattered and wandered on all sides. On
looking up, Santschi saw that the moon was obscured by a small cloud.
As soon as the cloud passed, the ants resumed their northward direction,
though now they were separated by greater distances. A second time
the moon was hidden, and a similar perturbation took place among
the ants, and on the moon appearing again, the former direction was
resumed, the ants then reaching a grass border and disappearing from
view. Thus these ants, removed to unknown ground, at once took
the moon as guide, and its momentary eclipse by a cloud was sufficient
to lead them astray.
Finally the author considers orientation by means of the stars
during the night, in twilight and in full daylight. (a) Stellar orienta-
tion during darkness. Here we may divide ants broadly into 38
categories, (1) species of a dark colour, in which the predominant
colours are black and red, because these colours best prevent the
penetration of the chemical rays of the sun. These species for the
most part are diurnal and possess well-developed compound eyes; (2)
pale and blind species living mostly underground, with which we are not
concerned here; (8) pale species with well-developed eyes. ‘These
come out at night time, or in the shadeof woods. There are, it is true,
some of this category that come out in full daylight, but they are
protected by a thick pubescence (eg., Cataglyphis bombycinus).
164 THE ENTOMOLOGIST’ S RECORD.
Yellowish species such as Camponotus thoracicus come out very rarely
during daytime, but often are found walking on the sheet on which a
lamp is placed to attract flying insects on moonless nights, and it is
well-known how often the winged sexes of ants will come to light at
night. In Tunisia during summer nights, even moonless ones, great
numbers of workers habitually come out. What then is the function
of these large compound eyes in nocturnal species, eyes often larger
than in allied diurnal species? From experiments made by placing
screens over ants on the march, either in daylight, or after sunset and
before the appearance of the stars, Santschi concluded that it is probable
that there is something in the sky itself, apart from the sun and the
moon, that can serve ants for a guide. When a cylindrical screen, 7.c.,
one hiding the surrounding ground but not hiding the sky, is placed
over an ant, the ant continues her way undisturbed, but when a
horizontal screen is held for a moment so as to hide the sky, the ant
at once becomes disturbed, wanders round, and is plainly at a loss for
the right direction. It must be noted that on nearing the nest, or
known ground, the cylindrical screen may derange the ant, because on
arriving at known ground the insect avails itself of georamic orienta-
tion and no longer depends on the sky.
The author is led to the conclusion that ants can see stars in
daylight. Stars may be seen in daytime from the bottom of a deep
well; the eye of the insect is composed of numerous tiny wells
directed to all points of the sky. In dealing with the objections to
his hypothesis, which he first stated in 1918, Santschi investigated
the wide-spread idea of stars being visible from a well, but this
phenomenon, if actually possible, appears only to be so under certain
conditions and under favourable circumstanees. Stars can however
undoubtedly be seen during an eclipse of the sun, and it is well-
authenticated that under certain conditions stars can be seen in
daylight without an eclipse, from the top of mountains or by reflec-
tion in mountain lakes. It is clear therefore that star-light traverses
the atmosphere in daylight, and the fact that we can enly see it rarely
is due to physiological not physical causes.
In support of his theory, the author goes into a careful anatomic
and physiologic survey of the eye of the ant.
In conclusion, he says it is perhaps because he lives in a flat,
“ desert ’’ country that he has been led to the discovery of sidereal
orientation, because in such a country landmarks are low, and there-
fore not suitable for use as distant guides to finding the way.
While sidereal orientation is not found in all ants, it is not confined
to these insects. Nesting hymenoptera return to their nests in a
direct line from considerable distances, aud where the conditions
exclude georamic orientation, astral vision may be the sole agent.
Experiments on a Scolia flavifrons gave results similar to the experi-
ments on ants.
Sidereal orientation appears to be the cause of the relatively large
development of the eyes in desert-living ants. The sand, constantly
disturbed by the wind, is a bad preserver of topochemical traces, and
under these circumstances ants are obliged to have greater recourse to
sight.--W.C.C.
(Mémoires de la Societe vaudotse des sciences naturelles, No. 4, pp. 187-
176, 1923). Bey pene oe
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BAGK VOLUMES OF
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(Vols. I-XXXYV.)
CONTENTS OF Vol. I. (Most important only mentioned.)
Gents dcronyetu and its allies.—Variation of Smerinthus tiliae, 3 coloured plates—
Differentiation of Melitaea athalia, parthenie, and aurelia—The Doubleday collection—
Parthenogenesis— Paper on ‘Y'aeniocampidae—Phylloxera—Practical Hints (many)—
Parallel Variation in Coleoptera—Origin of Argynnis paphia var. valesina—Work for the
Winter—Temperature and Variation—Synonymic notes—-Retrospect of a Lepidopterist
for 1890—Lifehistories of Agrotis pyrophila, Epunda lichenea, Heliophobus hispidus— —
Captures at light—Aberdeenshire notes, etc., ete., 360 pp.
To be obtained from—
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CONTENTS.
Seasonal Notes on the Rhopalocera, S. G. Castle-Russell, F.E.S.
The Variation in Larentia (Thera)*variata, by Carl Hifer (concluded)
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This Famous Collection—one of the greatest and richest in tho world—
comprises all the Families of the Macro- and Micro-lepidoptera of the whole
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Bexley | lL. WW. NEWMAN [Kent
Has for sale a superb stock of 1920 specimens in fine condition, including Varleyata ;
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aria, Abietaria; Irish forms Aurinia and Napi, fine vars. Tiliae, Yellow Dominula, etc.,
etc. Quotations and Insects sent on approval with pleasure.
Also a huge stock of fine PUPA and OVA.
Write for latest price lists.
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SEASONAL NOTES ON THE RHOPALOCERA. 165-
Seasonal Notes on the Rhopalocera.
By S. G. CASTLE-RUSSELL, F.E.S.
So far as my own experience goes the season has been an exceptionally
bad one, one of the very worst that I remember during the last 30 years.
The summer has been cold, windy, and sunless, and following upon
two very similar ones has no doubt had a very deleterious effect upon
insect-life generally, even the wasps being conspicuous by their absence.
The want of sunshine prevented the butterflies from moving about and
exercising their usual functions of reproduction. I particularly noticed,
about August the 20th, a large number of freshly emerged female
Polyommatus (Agriades) coridon and within three days, owing to the
wet and very cold winds, they had practically all disappeared, there
being no opportunity for ovipositing. This surely must affect the
numbers of next year. I have found in this district every species
scarce, with the exception of Cupido minimus, which was abundant. P.
(A.) coridon which was abundant everywhere around here four years
ago, has been very scarce, and in some spots has hardly appeared at all.
The Argynnids, also generally abundant, have been in dozens where
they usually appear in hundreds.
In the New Forest Dryas paphia has been scarcer than I have ever
seen it, and during the whole month of July only one good aberration
was seen, but not taken. Argynnis aglaia and A. cydippe (adippe) were
seen but rarely. Aphantopus hyperantus was in fair numbers and some
nice aberrations were secured. My wife saw a beautiful silvery grey
female Hpinephile jurtina sitting on a bramble-bush, but made an
unsuccessful effort to catch it, owing to the suspected presence of an
adder in the near vicinity. At the end of the season the Vanessas
were abundant and [ heard of two remarkable aberrations being seen
in gardens in this district, but not taken as no net was available.
My wife and I expended a very considerable time in field work
entailing much hard walking, and during the season we were fortunate
enough to capture the undermentioned aberrations which, together with
many others of a minor character, constitute a very satisfactory addition
to our cabinets.
Brenthis enuphrosyne.—Basingstoke. A male with the hindwings
on the upperside of a light straw colour.
— Argynnis cydippe (adippe).—New Forest. A male with the greater
part of the wings on the upperside of a straw colour.
Argynnis aylaia.—Andover District. A silvery white male. This
insect was seen one day and caught during a visit to the same down
three days after. When first observed in flight it greatly resembled
Boarmia roboraria.
- Aphantopus hyperantus—New Forest. 1. A male with large
symmetrical buff coloured splashes on outer portions of each under-
side wing: this is a very unusual form.
2. A remarkably fine male form of ab. lanceolata; the large pear-
shaped spot with a long white dash in the centre of the hind
wing, which usually has a small spot connected to it above, has an
additional spot beneath, there being a combination of three, instead of
the usual two spots
| Epinephile tithonus.—Andover District. 1. A male with one upper
wing of white coloration. i
Decemper 15rn, 1924.
166 THE ENTOMOLOGIST’ S RECORD.
2. A female with two upper wings white except portions of the
inner margins.
Polyommatus icarus—Andover District. 1. A gynandromorphous
specimen with the left upper wing entirely of male colour, the remain-
ing three wings being of female colour (brown) with dashes of male
colour on each.
2. A male so heavily dusted with black as to give the appearance
of dark blue.
Polyommetus (Agriades) coridon.—Andover District. A number of
males of a greenish colour, heavily dusted with black.
Two males and two females ab. fowler? all well-defined forms.
A female with underside upper wing striated.
A female with underside lower wing striated. —
A female with the wings one side normal: on the other side the
upper wing is striated and the lower wing obsoleta-form with white
ground.
In addition to the above described captured forms we were fortunate
enough to breed several very striking forms of Melitaea aurinia.
Melitaea aurinia.—Hampshire. 1. Female. On the upper wings
the usual fulvous colour is very heavily suffused with black, the hind-
wings being almost entirely black with series of elongated straw-coloured
spots. The underside is entirely spotless, the wings being of a light
fulvous: on the lower wings is a broad white border occupying about
half the area of the wings. This specimen is very similar to one I
bred last year, which was described by Mr. Frohawk in the Entomologist
of May, 1923. The underside of tbis latter specimen instead of being
spotless was heavily striated with black.
2. Female. The upperside of this is somewhat similar to the one
above described, but with less black suffusion, and the underside is of
more normal type, with the exception that on the upper wings there are
four large black spots on each, in addition to the usual spotting.
3. Female. This is a difficult insect for a non-technical person to
describe properly. On the upper wings the general ground-colour is of
a light rosy tint with long rays of a greyish white colour. The hind-
wings are nearly entirely black with 12 long pinkish grey streaks. On
the underside the upper wings are fulvous with the outer margins of a
rosy hue, the lower wings have a wide white border occupying the
greater part of the wing. The underside is entirely spotless. This
insect has a singularly beautiful appearance.
4. Male. The upper side of all the wings are fairly normal except
that there is an entire absence of yellow colouring. All the wings
have a wide entirely black border, without spotting.
All these specimens were bred under normal conditions in an
unheated green-house in the garden and which, owing to the absence
of sunshine at the time, did not greatly exceed the normal temperature.
All the imagines emerged in mid-May, about a week before the butter-
fly was on the wing in a wildstate. I have bred this species for several
years past but my experience has been that striking aberrations are
very rare, and this seems borne out by the fact that no really extreme
aberrations were included in the recent sales of famous collections.
| Aglais urticae. A late brood of larvae was taken on September 7th,
and produced a number of unusually dark types, the best being several
THE VARIATION IN LARENTIA (THERA) VARIATA, SCHIFF. 167
ab. bolandii on which the blue marginal spots are very large and
extremely bright.
It may be of interest to note that on Tuesday last a number of very
remarkable named forms of aberrations of the Vanessas were sold at
Steven’s Auction Rooms.
Forms of EFuvanessa antiopa, Hugonia polychloros, Pyrameis atalanta
and Aglais urtieae, varying beyond one’s wildest imagination were
included. These specimens were of Continental origin, and the result
of submission to extremes of temperature.
It was interesting to note that the well-known collectors present
fought shy of the insects, and they realised only a matter of a few
shillings each, an unsatisfactory reward for the labour entailed. One
collector was heard to remark that probably in a few years time some
of these specimens would be found re-pinned and re-set in British
collections improperly labelled. I sincerely trust not: anyhow they
will be easily recognised for what they are I think. [Some of these
were bought for a collection of Palaearctic Rhopalocera.—H.J.T.]
The Variation in Larentia (Thera) variata, Schiff.
By CARL HOFER of Klosterneuburg (Vienna).
(Translated by Hy. J. TURNER, F.E.S.)
(Concluded from p. 154.)
Nots.—In the foregoing portions of the article, by the name ‘‘ pine’’ is meant
Abies (Picea) excelsa (Féhren) Spruce, and by ‘‘ fir’’ is intended Pinus sylvestris,
scots’ pine, Fichten.—Hy.J.T.
To this I must add the foliowing notes from my own experiences.
1. The assertion is not true that an intermediate form is never
found—at least among the imagines in our neighbourhood (Vienna)—
between variata and obeliscata. In my own collection there are two
males of variata identical in their coloration with the obeliscata of
Herrich-Schiaffer’s figures. I have a similarly large and similarly
coloured example of obeliscata, placed with them to show that on the
other hand the insect affords quite a different impression.
2. That the food plant has no effect upon the colour, the insignifi-
cant results obtained by my colleague Preissecker and myself in breed-
ing from the egg have established. | have five variata of both sexes
which were reared from the eggs of a normally coloured and normally
marked variata female, and fed exclusively on Pinus sylvestris (FOhren).
These examples show very evidently not the slightest trace of an
approach to obeliscata. Further, I have a female of obeliscata, which
was bred from an egg laid by a female caught on the Buchberg, near
Klosterneuburg, exactly agreeing with the figure of Herrich-Schiffer.
The larva was exclusively fed on Abies excelsa (Fichten), but there was
no indication of the appearance of an obeliscata origin.
It is of no good to introduce into this question a parallel between
Ellopia fasciaria and obeliscata.. In woods of Pinus sylvestris (Fohren)
the brown form Ellopia fasciaria is found flying together with its
green form prasinaria; and these prasinaria, which fed on P. sylvestris
of course, are as deep green as the true prasinaria found in woods of
Abies excelsa (Fichten), where only the form prasinaria is found.
168 8 ! f THE ENTOMOLOGIST S RECORD.
But if the food really mfluences the colour why then are not.all the
P. sylvestris (F6hren) fasctaria brown ?
3. The statement as to the time of appearance is wholly unreliable.
With us (Vienna), in favourable years, one can rely upon meeting with
the first variata well at the end of April—what is stated of the rest of
Kurope in the literature ought certainly to be that of the whole of
Central Europe. ‘The end of May and June then is the chief time of
the appearance of the first generation, the few belated examples in
July follow with larvae of great diversity of development. At the end
of August and in September, even right into October, an intermittent
and weak second generation appears. But we—my colleague Preis-
secker and I—have observed in the open, and bred from larvae, only
one generation of obeliscata, Relative to a second generation reported
by a few authors, it may easily be the chance, that somewhat worn
specimens of Larentia firmata, which frequent exactly the same locali-
ties as obeliscata, were confused with the latter. I myself have occa-
sionally got in exchange firmata for obeliscata, and I have two pairs of
firmata now before me, to prove that a confusion, especially in the
female, is by no means improbable.
4. As to the supposition relative to the influence of the softer or
drier food on variata there is no confirmation. Both my colleague
Preissecker, and I myself, have obtained variata last year in confine-
ment in January and February. Then it quite often occurred, as it
can in the life of the free larvae, that for days at a time no fresh food
has been provided for them, and just as in our case with hard, dry war-
food, they had to be satisfied. But the resultant imagines all proved to
be recognisable indubitably as varzata.
As for the remarks of Treitschke, they are not, for the most part,
founded upon his own observations, and I think also, moreover, that
the information to be found in literature concerning the biological
circumstance of variata and obeliscata, especially for neighbourhoods,
where Abies excelsa (Fichten) and Pinus sylvestris (FOhren) are mixed,
must only be considered as really correct, when it originates from
absolutely reliable sources.
What evidence do our own observations in the open afford? We
have variata in numbers always exclusively in fir Abtes eacelsa, (Fichten
or Tannen) woods, but obeliscata is always met with confined more
exclusively to Pinus sylvestris (FO6hren) woods. The imagines from
larvae beaten from Abies ewcelsa (Fichten or Tannen) produce only
variata, without intermediates. Variata appears every season a few
weeks earlier than obeliscata. Of the former there is always a second
—if only a partial—generation in the autumn, of the latter we can only
establish the occurrence of one generation.
These observations, so far as one can say, have been made by abso-
lutely reliable guarantors, also for most other neighbourhoods ; for
instance, Louis B. Prout’s statements in his article appearing in the
45th volume of the Hntomoloyist, in numerous quotations as well as
German literature-citations. Prout knew only a single entomologist
who had obtained obeliscata from Abies eacelsa (Fichten), and this was
Mr. Raven, of Cambridge, already quoted by me. This information
now must be received as quite reliable, since he confirmed it afresh in
vol. 46 of the Entomologist, of the year 1913, what he had himself
stated for Prout’s article, that he, from a number of larvae, which were
THE VARIATION IN LARENTIA (THERA) VARIATA, SCHIFF. 169
exclusively beaten from Abies excelsa (Fichten), and furnished the same
as food-plant, bred both typical variata, just as Prout figured in his
article, and typical obeliscata.
Concerning the larvae of variata and obeliscata, so very variable are
they, that we cannot separate them by any definite, constant, charac-
teristic differences.
Finally, Herr Prof. Dr. H. Rebel and Dr. H. Zerny have, at my
request, kindly undertaken an examination of the male genital appa-
ratus of the three chief forms of the variata group, and what they have
communicated to me is placed below.
“The male genital apparatus in the Larentia variata group is con-
structed on a single plan and uniformly shaped.
‘‘The uncus has the form of a very long, outwardly curved thorn.
A scaphium does not stand out as an independent morphological struc-
ture. The extended, distally spoon-shaped, spreading valves bear on
their inner margin before the first half of the length, a simple pair of
fibulae with their apices converged towards one another. In connection
with these there stands a much more slender chitinised pair of struc-
tures, in the form of a stalked long-bristled pad (2nd pair of fibulae).
A heel on the latter more dorsal lying structure is wanting. As the
penis duct functions a distal fold appears in one angle.
“The penis is a distal strongly enlarged chitinous tube, of which
the distal end is furnished with a border of strong chitinous
‘spines (thorns) lying along the tube. These penis spines, varying
jin number and position, afford but only individual variations. From
this it appears the assertion of Prout differs (Seitz., Vol. IV., p. 217),
in which he states in the case of obeliscata, ‘The spine group on. the
aedoeagus differs from that of the 9 of vartata.’
“Investigation was made of the genital apparatus of two each of
variata and obeliscata and of one stragulata. A very general con-
formity of the preparations was so apparent that no further prepara-
tions were made.”
If now no doubt still appears to exist as to a slight affinity between
variata and stragulata, we may probably recognise in the obeliscata-
form, retaining itself so different in its biological aspect, in spite of the
conformity in structure of the genital apparatus, a species in the
making before our eyes, on account of its tendency to isolation.
It would be equally interesting to establish crossings between
variata, obeliscata and stragulata, from the results of which probably
further conclusions could be demonstrated. Possibly there would
arise from such an investigation a conclusion as to which of the three
forms, is genetically the oldest.
I will, at any rate, myself endeavour to undertake such an investiga-
tion, and it would be a very great pleasure to me if my work were to
induce my dear collecting colleacue to the same object.
In conclusion I ask all who have aided me in the composition of
my small contribution to accept my best thanks. But especially do I
tender my thanks to Herr Prof. Dr. Rebel, who in spite of the prevail-
ing intolerable temperature of the unheated rooms of the museum
library, in an unselfish, devoted way, afforded me an introduction to
the rich collection of literature, and helped me with it.
170 THE ENTOMOLOGIST’S RECORD.
GYURRENT NOTES AND SHORT NOTICES.
Eintomotocy at WemBLEY.—One might mention, in addition to the
interesting account given by Mr. Harry Moore in our last number,
that Professor EK. B. Poulton, F.R.S., had an exhibit, No. 207, illus-
trating Mimicry in an African Swallowtailed Butterfly (Papilio dar-
danus); and Dr. C. J. Gahan an exhibit, No. 208, on Mimicry in
Beetles. These two exhibits will be found described in the excellent
little Handbook to the Exhibition of Pure Science, arranged by the
Royal Society. In this publication also, p. 127, Professor Poulton
writes a short article on Insect Mimicry and the Darwinian Theory of
Natural Selection.
It will be remembered that the ant Camponotus (Myrmotrema)
perristi, Forel., subsp. nigeriensis, Sant., recorded by Mr. Crawley and
myself [Hnt. Rec., 36, pp. 91 and 92 (1924)]|, was captured in some
numbers by me in the case containing the termitarum and driver-ants
in the Nigerian Section, referred to by Mr. Moore.—Horace Donis-
THORPE.
A very successful meeting of the Entomological Club was held on
November 4th, at No. 8, Lancaster Place, N.W. 8, the residence of Mr.
H. Willoughby-Ellis, F.Z.8., F.H.8., the Hon. Secretary of the Club,
and the host of the evening. The other members present were Messrs.
Robert Adkin, Jas. E. Collin, H. Donisthorpe, Dr. H. Eltringham, and
Prof. E. B. Poulton. Im addition the following guests were present.
Messrs. F. Balfour-Browne, EH. C. Bedwell, K. G. Blair, Dr. EH. A.
Cockayne, Messrs. E. Krnest Green, Philip Harwood, Dr. A. D. Imms,
Dr. S. A. Neave, Capt. N. D. Riley, Messrs. Rait-Smith, W.G. Sheldon,
and Hy. J. Turner. The visitors were received by Mrs. Willoughby-
Ellis in the drawing-room, where tea was served. An inspection was
made of the host’s private museum, especially of the collections of
Coleoptera, Hemiptera, and Lepidoptera, which were very complete,
many rare and local species being either of his own collecting or
obtained by well-known collectors. During the evening the fine
original drawings of Tineina and of Staphylinidae, by the late John
Sang, were on view. The original drawings of the late John Scott
and of the late A. Matthews, of the figures published in their
respective entomological works were also on view. Supper was served
at 7.45, and at a late hour the very pleasant gathering closed.
Prof. Giacomo Cecconi, Director of the Royal Regional Observatory
of Fano, Italy, has just issued an admirable treatise on Forest Hnto-
mology (Manuale di Entomologia Forestale) consisting of XX.+680
pages with 786 figures in the text, many very beautiful photographs
mostly original. The cost is 120 lire. There is an introduction by
the well known entomologist, Prof. B. Grasse.
Subscribers will no doubt see again in the present issue the
advertisement of the great Oberthir collection in France. It has been
offered to the National Museum of France at a moderate figure as a
whole, we hear, but was refused, hence the advertisements now issued.
Intending buyers of species, series, families, groups, etc., must write to
Rennes for particulars. Our contributor M. Carl Hofer will send all
information if one writes to him at Imprimerie Oberthtir, Rennes,
France.
Signor Querci has returned from his Spanish tour with an extremely
CURRENT NOTES. 171
large collection of butterflies and moths colleeted by himself, his wife,
daughter, niece and latterly Dr. Romei. Tripolitania was worked by
the last and latterly by Sig. Ederli, and large collections were obtained
there. To those working on the Mediterranean section of the
Palaearctic Region there is a fine opportunity to obtain species and
races somewhat difficult to get by the average business man, whose
continental collecting must be limited to his annual holiday.
In the Revue Mensuelle de la Société Entomologique Namuroise, M.
Derenne describes and names anew form of Pieris napi as ab. elongata,
in which the wings are teratologically affected, all four wings being
elongated with a waved outer margin. In so doing he follows the
action of M. Gelin, Soc. Ent. Fr., 1914, in naming a similar aberra-
tion (cripple) of P. brassicae.
Dr. Holland, in the Entomological News for October, reports the
occurrence in numbers of Hurrhypara urticata, from Machias, Maine.
This species is not included in Dyar’s List of Lepidoptera of North
America.
It is curious that Papilio podalirius is an indigenous species in
Belgium and is not found even in the southern part of Great Britain. In
the Rev. Mens. M. Derenne discusses the question of generations, and
on all the evidence falls back on the statement of the late M. Lambil-
lion, that there was only one generation of P. podalirius in Belgium,
in May-June, and that the occasional specimens obtained later were
individuals retarded, for some reason or another, in their appearance.
Nomenclature is a complicated question. The editor of the H’ntomo-
logieal News calls attention to a recent remark by Dr. Holland, that
‘the laws of priority do not have precedence over the laws of correct
language,’ and he (the editor) asks the following cogent question,
«« Are names in biology convenient and arbitrary tags to designate
material things, or are they a field for linguistics?” He further remarks
that our ‘‘great needs in nomenclature are stability, and finality which
leads to the former.’’ The obvious comment is that if the classical fiend
is let in to the controversy there will never be finality, and we shall be
further off than ever from stability.
SOCIETIES.
Tue EnromonoeicaL Society oF Lonpon.
October 15th_—Excrion or Fritows.—The following was elected
a Fellow of the Society:—Mr. EK. P. Sharp, 1, Bedfordwell Road,
Kastbourne.
Aureration or Byz-Laws.—The Secretary read for the first time
the alterations in the Bye-laws proposed by the Council.
Exuiprrions. —The President exhibited intermediate forms between
typical Pachys betularia and var. doubledayaria bred from wild larvae
taken at Camberley.
Mr. H. Donisthorpe exhibited a number of insects and other
Arthropods found associated with the ant Acanthomyops brunneus in
Windsor Forest.
The Secretary, on behalf of Mr. C. Dover read a summary of
observations by Dr. H. Brauns on the habits of some South African
Carpenter- bees.
Dr. K. Jordan exhibited some beetles of the genus Urodon and
172 THE ENTOMOLOGIST S RECORD.
discussed their systematic position, expressing the opinion that they
belonged to the Bruchidae rather than to the Anthribtidae.
Professor EK. B. Poulton, F.R.S., discussed further evidence of the
pale yellow fluorescent pigment in the males and primitive forms of
mimetic females of ‘Papilio dardanus. He also read a letter from Mr.
R. H. Harris throwing further light on the attractiveness of dummy
animals to T’setse-flies discussed at the meeting on May 7th, 1924.
Mr. J. J’ Lister exhibited a fine series of Teracolus nouna and the
local form of Lycaenopsis aryiolus from Algeria.
Mr. W. J. Lucas, on behalf of Mr. G. Bateson, exhibited examples
of a rare dragonfly Leucorrhinia dubia from Surrey.
Paprers.—The following papers were read :—
(1) On Australian Histeridae (Coleoptera), by Mr. A. M. Lea.
(2) On the Morphology of the Male genitalia in Rhynchota, by
Hem Singb Pruthi.
(8) Some aspects of the Biology and Morphology of the Neuroptera,
by Dr. C. L. Withycombe.
(4) Notes on the Orthoptera in the British Museum. No. 4, by
Mr. B. P. Uvarov.
Tue Sours Lonpon EnromonocicaL Society.
September 25th.—Exuipi1ion oF ORDERS OTHER THAN LEPIDOPTERA.
—Mr. Robt. Adkin exhibited specimens of a Collembola he believed
were referable to Podura aquatica. It was common in his garden at
Eastbourne.
Mr. W. J. Lucas, coloured drawings of the Naiads of the dragon-
flies Aeschna juncea and Agrion mercuriale,
Mr. Hugh Main, living specimens from 8S. France of (1) Mphippigera
sp., gd and ?, both of which stridulate; (2) two species of Mantis, one
of which was M. religiosa, the female had not eaten the male, as, he
suggested, they were well supplied with food; (8) Scavabaews sacer, Corsica,
common near goat’s dung, with their ‘pear balls” and pupae; (4) the
larva of a Myrmeleon sp., common on the Mediterranean shores; (5) @
? of the large wolf-spider, Liycosa narbonensis, with her family on her
back; (6) and the banded spider, Hpetra fasciata, with her egg-cluster.
Mr. B. Williams, Coleoptera from Wicken, Harpenden, Luton, and
Bricket Wood.
Mr. O. R. Goodman, a brown Viper taken at the Field Meeting at
Westerham, on September 13th.
Mr. S. R. Ashby, the Carabus intricatus taken in 1857 by the late
Mr. Reading ; and Calosoma sycophanta taken by Mr. Tugwell, jun., at
Freshwater, in 1878.
The almost complete collection of Paraneuroptera from the Society’s
cabinet was on view.
Mr. H. W. Andrews, a long series of a very scarce Asilid dipteron,
Entolmus rufibarbis, from N. Kent, and a number of typical specimens
of Anthomytidae and Empidae he was presenting to the Society’s
reference collection.
Mr, R. A. R. Priske, series of several specimens of Helix (Mollusca)
from High Wycombe, and H. acuta from Sussex.
Mr. Stanley Edwards, the giant hemipteron, Macroceraea sp., taken
by Mr. Dawson in Tenasserim, and the striking Lycaenid Lohita
grandis.
SOCIETIES. 173
Mr. Enefer, a cactus dahlia sport, a red and a yellow flower on the
same stem ; an embryo of the Cocoa-nut; and an embryo of the Date
Palm.
Mr. L. . Dunster, an underside of Polyommatus (Agriades) thetis
with forewings striated and hindwings normal, except that the ground
colour was whitish.
Mr. H. Moore, various species of Ants, including Camponotus hercu-
leanus, the largest Huropean species, and stink ants, stinging ants, leaf-
carrying ants, and foraging ants.
Mr. 8. Blenkarn, four boxes containing many species of Coleoptera
from his collection.
Mr. H. Willoughby-Ellis, several species of Carabus (Col.) which
showed melanic aberration, and also several maritime species which
occasionally were met with inland.
October 9th.—Mr. R. Adkin read a paper, ‘‘ Entomology: Ancient
and Present-day,’ and illustrated it with many slides of portraits of
ancient naturalists, and of plates and pages from old and famous
works.
Mr. Step exhibited the vaulted earth-star fungus (Geaster minimus)
from Mickleham, found on the Foray on October 4th, and new to the
British List.
Mr. A.A. W. Buckstone reported the second flowéring of rhododen-
dron on Netley Heath.
Captain Crocker exhibited a 2 of Polyommatns (Agriades) coridon
with distinctly blue hairs covering its abdomen, with many other Roys-
ton aberrations, and an aberration of P. (A.) thetis underside forewing
ab. obsoleta, and hindwing ab. striata.
PBEVIEWS AND NOTICES OF BOOKS.
‘‘Tie Monpe Soctan pes Fourmis pu Guosr,”’ by Dr. Auguste
Forel, Geneva: Librairie Kundig, Kditeur, Tome 5°, 1923. Pp. I-VI.
+174; 2 coloured plates, 1 black and white plate, and 30 text figures.
—This, the fifth and last volume, treats of the specialised habits of
ants, followed by an Epilogue on Ants, Termites, and Man! The
frontispiece is a reproduction of a recent photograph of Dr. Forel in his
study.
There are as usual seven chapters ; briefly as follows :—
Ch. I. The wars of driver ants, or Dorylinac, against other
living beings.
Ch. Il. ‘The granaries of harvesting ants.
Ch. III. The Attini; ants which cultivate mushrooms.
Ch. IV. Weaving ants.
Ch. V. Ant door-keepers.
Ch. VI. The Rhagomyrmicinae.
Ch. VII. Diversa.
(1) The Ponerinae.
(2) The Pseudomyrmint.
(3) The Cremastogastrini.
(4) The Pheidole.
(5) The tree ants.
(6) Ants of the deserts and steppes.
174 THE ENTOMOLOGIST’ S RECORD.
(7) Agile and sluggish ants.
(8) Jumping and projecting ants,
The Epilogue.
Cuapter 1.—Good descriptionsare given of the well-known raids and
habits of the formidable Driver-ants (Annoma) of Africa, etc,, and the
Wander-ants (Hciton) of S. America, etc. The author refers to and
quotes some of the observations of Bates, Belt, Bruch, Muiler, Savage,
Vosseler, etc., and gives an account of his own experience with Dorylus
(Lyphlopone) fulvus in Tunis, in 1889.
Speaking of Dorylus (Alaopone) orientalis in India, he says that it
appears to be herbivorous and not carnivorous, and that according to
Green it eats the bark of trees and various tubers, such as potatoes,
etc. He adds, however, ‘This requires confirmation, although Green
was a good observer.” Our friend Mr. Ernest Green tells us that there
is not the slightest doubt about this. He has observed it himself over
and over again, both in his own garden and elsewhere, in Ceylon. The
habits of the quite eyeless genus, Aenictus, are given, chiefly from the
observations of Wroughton. They are more subterranean than Dorylus,
and their military organization is said to be more perfect.
Finally the Leptanillini, the smallest ants in the world, are dealt
with. ‘These tiny creatures hide under stones, and probably hunt the
very smallest living beings.
CHarrer I].—Gives an account of the ‘‘ Harvesting ants.” The
writings of Solomon are quoted (as the author truly remarks, he was
more observant than some of the scientists at the beginning of the last
century), as also those of Horace, Virgil, and others of the ancients.
The ‘‘Seed-Collectors” belong to the Myrmicinae; in Kurope chiefly
ants of the genus Messor; in Asia Halcomyrmea and Pheidologeton ; in
America Pogonomyrmeax; and numerous Pheidole everywhere; some
Solenopsis, and others.
The observations of Sykes (1829) and Jerdon (1851) are referred to,
and a good account of the work of Moggridge (1871-2), at Mentone, on
two species of Messor, and Pheidole pallidula, is given. Mogeridge also
mentioned that Lasius emarginatus and Tetramorium caespitunt occa-
sionally stored seeds; and Forel himself once found a granary of Lasius
brunneus at Martigny. In the same way we have several times found
T. caespitum storing seeds in England.
Next the more experienced experiments of Hmery in Italy, and
Wheeler in America are related, and finally Laméere’s interesting
observations on the harvesting ants of the Sahara are recapitulated.
Cuapter IIJ.—This is a very interesting chapter, dealing with the
“ Teat-cutting Ants’ (Attint), which cultivate mushroom gardens, and
the observations of nearly all the workers on the subject are referred
to. Forel, when recording his own experiences in Colombia, mentions
that Trachymyrmex marthae carries the petals of flowers into its nests.
This reminds us that we once found A. (D.) fuliginosus at Woking
carrying the petals of the privet into its nest; and though of course it
does not cultivate fungus gardens, a fungus does grow on the walls of
its carton nests.
On page 86 he says that the fecundated ° ¢ of Aéta fight together
and mutilate each other; whereas, in his third volume, he said he did
not believe this.
As an appendix to this chapter a resumé of the recent discoveries
REVIEWS AND NOTICES OF BOOKS. 175
of Dr. Carlos Bruch, at Buenos Aires, is given.
Cuapter 1V.—This is quite a short chapter, devoted to those ants
which use their larvae as spinning machines to fasten together leaves,
etc., to form their nests.
Forel truly says that the Englishman, Ridley, first discovered this
remarkable fact in 1890, and he also refers to the work of Doflein,
Dodd, Bugnion, Goeldi, and Jacobson, on the subject. The list of the
observers in their proper order should read as follows :—Ridley (1890) ;
Savil Kent (1891); Hammond (1900); Green (1900); Dodd (1902);
Chun (1908); Doflein (1905); Goeldi (1905); Jacobson (19085) ;
Karawaiew (1906); Bugnion (1908); O’Brien (1910); and Wheeler
(1914).
The ants which practice this remarkable habit belong to the genera
Oecophylla, Polyrhachis, and Camponotus, which are all in the sub-
family Formicinae. This phenomenon is perhaps most widely known
with the first named genus, and the author reproduces some of Dof-
lein’s figures, showing a worker ant holding its larva; a number of
workers holding aud sewing together two leaves; and the silk glands of
the larva. Forel explains how, if two leaves are too far distant from
each other, the ants form a chain by each grasping a fellow-worker by
its long petiole. He mentions that Bugnion has given a drawing of
one of these chains (but Green also published an account of the same)
in Ceylon. Wheeler has suggested that this habit may account for the
very long petiole possessed by these ants. Finally an account is given
of various kinds of Polyrhaehis nests spun together with larval silk.
Cuapter V. is also a very short one. Forel explains that by the
term “fourmis portiers’’ he means the soldiers, or large workers, whose
special office consists in guarding the doors, or entrance to a nest,
either in the earth, or in branches, or carved in wood. He says they
only occur in the Camponotinae (should be Formicinae) and Myrmicinae.
There are all possible transitions between the door-keepers entirely
adapted to this purpose, and the semi-doorkeepers. The most perfect
examples occur in the sub-genus Colobopsis, in which the front of the
head in the soldier is cut off quite flat, and it fits exactly into the round
hole which forms the entrance into the twig, or wood, in which the nest
is situated. These forms Wheeler has most aptly called living front-
doors.
The author describes how he discovered this habit in the Huropean
Camponotus (Colobopsis) truncatus at Vaux, in 1872; and discusses the
intermediate forms, and how the more perfect cases have been
developed.
Carter VI.—Three tribes of the Myrmicinae—Cataulacint, Cryp-
tocerint, and Dacetini—are dealt with. In the first two the integument
is very hard, and the head and thorax are sharply bordered, no doubt
as a protection against other ants and differentenemies. The eyes are
hidden beneath the borders of the head, and Forel suggests that this
accounts for the fact (as observed by himself in Colombia) that these
ants are unable to walk in a straight line, like other ants can.
In Cryptocerus eduarduli the eyes in the female are flatter and
smaller than in the %, contrary to what usually occurs with ants.
The gizzard also in Cryptocerus is entirely unlike that of any other
Myrmicine ant. The males in the Cryptocerini are so entirely unlike
their @ @ and 8% 8, that they might easily be thought to belong to
quite a different family of insects.
‘176 THE ENTOMOLOGIST’S RECORD.
In certain Cryptocerini (of which a good figure is given) the 2 Q
and % % have the head not only enlarged, but cut off short, and
scooped out in front like a saucer. It is suggested that these species
act as front-doors in the same way as do Colobopsis species.
In the Dacetini the rule is for them to possess curiously formed and
long jaws, and the genus Strumigenys is said to use the latter for
jumping. Many of these species are covered with curious scale-like
hairs and spongy growths.
Finally the author points out that all the Rhagomyrmicinae present
a vast field for observation, and experiment, on their biology and
habits.
Cuapter VII.—This chapter embraces a number of observations
on many different and widely separated species of ants.
It is pointed out that in the Ponerinae the % 8 as well as the? 9?
and 3 g¢ are able to escape from their cocoons, and rid themselves of
the pupal skin unaided. Forel says that they neither rear plant-lice,
Coccidae, nor any other ‘‘ cattle.” We, however, have taken the coccid
Ripersia donisthorpeti with Ponera coarctata in England; and the colem-
bolid Cyphodetrus albinos, and several beetles, including Bythinus glab-
ratus (a regular guest of this ant), are found in its nests.
Tepper is said to have observed the marriage flight in Myrmecia,
but he [1882] only mentioned swarms of the J g and winged ? 9.
Wheeler, however [1916], gives a very graphic account of a remarkable
marriage flight of the “ Bulldog” ant Myrmecia sanguinea, observed by
Froggart, and described by the latter observer in a letter to him
(Wheeler).
The Ponerinae are mostly insect feeders, some specializing in Ter-
mites, woodlice, ete. We may mention that Wheeler pointed out in
1904 that Leptogeuys elongata is a crustacean-eater.
Under Pseudomyrmini, their habits are briefly dealt with. The
reasons why Wheeler separated this tribe from the Myrmicinae and
raised it to the rank of a sub-family (and also the Cerapachyini from
the Ponerinae), with which Forel does not agree, are only given as follows
—on his studies on the gizzard; the larvae ; and the feeding of the latter
by these ants. Wheeler, however, also pointed out that the shape of
the head, especially the clypeus and frontal carinae, is unique; the
eyes are very large, the construction of the petiole, post-petiole, and
tibial spurs is peculiar; and that the antennae are 12-jointed in the
g as well as in the 9? and %. We consider that not only was
Wheeler justified ; but that he entirely proved his case.
Under Cremastogasterini, a very compact group of Myrmicine ants,
the peculiarly flexible form of the abdomen, and their habits of con-
structing carton nests, etc., etc., are touched upon. The feeding
of gnats by these ants is also described and figured. In the painting,
however, on Plate I. (fig. d) the position taken up by the gnat is incor-
rectly represented! The fly should face the ant, with a posterior pair
of lees raised in the air [see Jacobson’s actual photographs, Tijd. v.
Entom., 54, Plates 12 and 13 (1911)]; whereas it is shown standing
over the ant, facing in the same direction, with all six feet touching
the ground.
The immense and widely distributed genus Phetdole (which
exhibits extraordinary polymorphism in the 8 8; the 2{ 2/ possessing
large heads, which are enormously developed in some species), and the
REVIEWS AND NOTICES OF BOOKS. 177.
nearly allied genera, are next touched on, and their terrestrial and seed-
collecting habits are pointed out.
A few remarks follow on various ants which inhabit trees, and the
old belief is quoted, that some species with very big eyes inhabit the
tree-tops. ‘‘Gigantrops”’ (should be Gigantiops) of Brazil is mentioned
as an example; but Wheeler (1922) has shown that it really belongs
to a forest-floor ant fauna.
The ants of deserts and steppes: agile and sluggish ants; and the
jumping species, complete the seventh chapter.
The epilogue runs to 35 pages and, with the exception of six pages
on the role of ants in nature, has little todo with these insects. The
author takes the opportunity of expressing his socialistic views, and
other eccentricities. On page 160 he speaks of the horrible ferocity of
our ancestors, and maintains that the orang-utans and gorillas are
truly angels in comparison. I might with more justice assert that
Nero, and all the tyrants of antiquity were angels of light compared to
the brutal Bolshevists who have utterly crushed the Russian peoples in
our own day. He refers to the immense numbers of human beings
destroyed during the great war, but says nothing of the post-war tragedy
of the 8,000,000 souls in Russia alone for whose death Lenin and his
bloodthirsty associates were directly responsible. [I should wish in
particular to protest against the ants being employed as a supposed
weapon in political controversy. In my opinion an entomological work
is not the appropriate channel for the introduction of views on social-
ism, or politics of any kind, still less as the means for their glaring
advertisement. Let those, however, who are so ready to set forth the
social life of ants as a lesson to human beings, and in favour of a
socialistic community ponder on the following facts :—To ali intents
and purposes the working classes of ants are sterile! They have no
trade-union rules; each worker does as much work as she can from
early morn to dewy eve, and often during the hours of the night as
well. All are willing to sacrifice their lives at a moment’s notice for
the good of the State, and areever industrious and contented. Insomeof
the harvesting ants the large workers possess enormously developed
heads in order to contain the powerful muscles of the jaws with which
they crush the hard seeds required for food; but when these workers
are no longer needed by the colony, the other ants cut off their heads
and throw them on the refuse heap! This is, as I have pointed out
elsewhere, a very drastic, but effective, method of getting rid of a
superfluous working class !
Forel maintains that the true queens of ants are the workers, whose
labour gives to them at once their royalty and liberty ; while they are
denied the marriages and debauchery which, according to him, form
the sole ideal of human queens. Was ever such libellous nonsense
written 2? Where is the Queen, who in the memory of any of us, has
ever spent such an existence ?—Horace DonistHorPE.
P.S.—Reviews of the first and second volumes of this work may be
found in the Hnt. Record, Vol. XXXIII., pp. 59-60 (1921), and Vol.
XXXIV., pp. 38-40 (1923) ; and the third and fourth in the Ent. Mo.
Magq., Vol. LX., pp. 89-98, 140-142 (1924).—H.J.D.
Correction.—Page 151, line 18 from the top for ‘‘specimen”’ read
“« species ’’ and for ‘‘ ardeanus”’ read ‘‘ aubeanus,”
178
.THE ENTOMOLOGIST’S RECORD.
CONTENTS OF VOLUME ae
By Hy. J. TURNER, F.E.S.
PAGE
Aberrations in, S. ligustri, 13; P.
atalanta, 29; T. pronuba, 29;
P. napi, 29; P.megera, 29; C.
pamphilus, 29; M. aurinia, 305
P. coridon, 30; A. caja, 30, 148;
Eggs of Blackheaded Gull, 30;
Z. filipendulae, 30; A. hyper-
antus, 42; M. tiliae, 42; LK. car-
damines, 42; P. dejeanii, 62; S.
ligustri, 64; H. marginaria, 64;
A. exclamuationis, 80; T. variata,
88; V. macularia, 129; C.
arvensis, 130 ; A. urticae, 143 ;
R. bifasciatum, 147; P. napi,
147; M. titea, 147; T. obeliscata
(variata), 153; B. euphrosyne,
165; A. cydippe, 165; A. aglaia,
165; A. hyperantus, 165; E.
tithonus, 165; P. icarus, 166;
P. coridon, 166 ; M. aurinia, 166 ;
P. thetis
Aberrations Mosaic, explained, 18 ;
List of, 19; Striate
He Aberrations Nouvelles de Coccin-
elles,’’ by J. A. Lestage.
Abnormal specimens of Lepidoptera
Abundance of Orthoptera in the
Alps, 59; of larvae Sic
Gr Additions and Corrections to List
of Grypocera and Rbopalocera of
Peninsular Italy,” yi Dr. R.
Verity ;
Affinities of Psychids :
Analysis of species of Taphrorychus
Ants, Lycaenid Larvae and, 8;
Castes, 44; Relation of, to other
organisms, 45; In I. of Man, 50;
Mixed colony of, 52; and Coleop-
tera, 69, 1383; and Diptera, 70;
Nigerian, imported into England
Asymmetry in 4. grossulariata
Autumn, Butterflies in Late, 143,
144; Captures
“ Batrisodes delaportet and B.
adnexus, two additions to the
British List of Poeapiera i by
H. Donisthorpe
Bee- Anatomy hes
Bees, Solitary and Social Sia
Biographical Dictionary, A. St
Boarmia abietaria at Gravesend ..
British Museum illustrations a
“Cannibal Coccinellid, omit by
Cc. C. Leman Bs
Classification, of Papilio, 132; of
Orientation in Ants :
Comparison of brood of P. thetis .
Contest, A Homeric..
“ Cumberland Coccinellidae,” by
PF. Marriner. 4 és. sis
. 173
30
155
33
143
5. 108
81
118
91
42
156
aly
16
43
11
26
11
60
161
116
11
85
PAGE :
Description of, ab. plwmbea of B.
euphrosyne, 8, 27; ab. aurata,
of H. variegata, 1; ab. triangu-
laris of H. variegata, 1; race
anglia of H. semele, 22; race
anglorum of H. semele, 22; race
paeninsulitaliae of H. semele, 24 ;
larva of 7. verhuellella, 65; B.
delaportet, 117; B. adnexus, 117;
T. villifrons, 118; larva of EH.
sinuata, 134; egg of S. longi-
rostris, 137; E. decipiens . 150
Descriptions, Barebones 115
‘« Digne and the Basses Alps, July
1923,” by Lt. H. B. Ashby, 102, 122
Dimorphic larva of a Nymphaline 64
Distribution of S. telicanus 10
Divergence of character query . 156
Double-broodedness in J’. punctu-
laria 143
Duplicated fore- -wing in Z. iii
pendulae : 30
Dwarf, H. pustulata 64
Early appearance of E. pumilata.. 26
‘« Hees in L. hirtaria, Yellow,” by
Dir A. Ei. Cockayne oy 149
Entomological Club, 115, 127, 144, 170
‘“* Hntomological Notes for the
Season 1923”’ by Comm. G. C.
Woodward ; 4, 20
Entomology in Russias 79: in
Armenia, 79; at Wembley 157, 170
“© Huchloé (Anthocharis) ausonia
(belia) and its second brood,’’ by
P. P. Graves 90
‘« Huplectus decipiens, a species of
Coleoptera new to Britain,’’ by
H. Donisthorpe 150
Foodplant of P. bifasciata, Unusual 158
Forcing of, P. aegeria, 116; D.
paphia . biG
Freyer on L. variata é 119
Generations of L. rivularis in Italy 127
‘‘ Geographical Variation in H.
semele,”’? by Dr. R. Verity 21
Genital characters of T. variata .- 168
Guests of Ants, 45, 49, 69, 121,133, 176
Gynandromorph of, Pe coridon, 30;
A. populi .. sal aO
Habits of, Water- bugs, ‘1b: L.
hirtaria, 61; L. grandis, 62;
Psychid Larvae, 98; larvae of
H. rostralis 130
Harpe, de la ,on mM ‘variata, 119 ;
Ants He 174
“« Hermaphroditism: ” in the Hes.
periidae : oo.
ee pep variegata,” by
G. B. C. Leman .. 1
6 nee in N.W. Cornwall, A, ”
by Cecil Worssam . 142
INDEX. 179
PAGE PAGE
Hybrid, Suggested, P. coridon and Rearing beetles in confinement 63
P. hylas é : .. 116 | Records of Lepidoptera from Witley
Hybrids, . 6, 29, 116 District of Surrey, Further, by
Immigration to the ‘Alpine region 59 W. H. Smith : 75
Inheritance in A. grossulariata 17 | References to Ant Literature . 138
Insect Control—an outline of the Relationship of Psychids, Suggested,
Principles 154 by Rev. C. R. N. Burrows Sil, C7
Irregular copulation of M. phoebe Rio de Janeiro Entomological
and M. didyma ae Las Society a 5¢ seu ly
Italian Entomological Society 12 | Reviews :—Fabre’s ‘‘ Book _ of
Lady-birds hibernating in the Insects,’’? 14; ‘* Some Habitat
House . 9.) 2H, Responses of the Large Water-
“ Larval habits of T. Meerintellelicn »3 strider, G. renugis,’”’ Curtis Riley,
by Alfred Sich .. 65 14; ‘‘ Practical Bee Anatomy,”’
Life-history of T. oenipenciaia . 65 A. D. Betts, 15; ‘‘Our Butter-
“Locality in the High Alps, flies and Moths and how to know
Névache-le-Chateaux, A,’’ by them,’’ F'. Daglish, 16; ‘‘ Social
W. Fassnidge 5 .. dd Life among the Insects,’’ W. M.
Longelivity of a beetle ao) | (3 Wheeler, 30, 42; Proceedings of
Luminous insects 63, 80 the 8. London Entomological and
Lycaenid larvae and Anta): ; 8 N. H. Society, 47; ‘* Life-work
Melanie B. repandata, 14; Mu. dict- of Ld. Avebury,” 93; ‘ Ants of
ynna, 29; D. paphia, 30; E. Timothy Thummel,’’ 93; ‘‘ Die
christyt, 30; C. autumnaria, 30; Lepidopteren Fauna Aegyptens’”’
IEK multistrigaria, 30; H. aefoli Andres and Seitz, 96; ‘‘ Bulletin
aria 5 atv) of the Hill Museum,’’ 131;
Migration, Congregation for 63 ‘‘Trans, Knt. Society of London,”’
Mine of L. verhuellella .. 65 145 ; ‘‘Verhandlungen Zool.-Bot.
Mimicry in W. African Lepldoptera 14 Gesells. Wien,’’ 146; ‘‘ L’Orien-
Myrmecophiles with 4. brunneus tation Sidérale des Fourmis,”’
121, 133 D. Santschi, 160; ‘‘Le Monde
‘“*Myrmecophilous Notes of 1923”’ Social des Fourmis du Globe,”’
by H. Donisthorpe da) EB Ge) Dr. A. Forel, Vol. V. .. oo dae}
New British Cecidomyiidae, by B.S. Russian Entomological Society,
Bagnall and J. W. H. Harrison The, Dr. M. Burr - heiie ahs)
36,53, 99 | Rare and very local species, #.
New forms of Coccinellidae .. 1, 155 Christi, 3; A. tinéana, 13; H:
New, Tinea, A, 63; Aphid, A 5 lei simplana, 13; Larinopoda sp.,
sé Nomenclature—1924 ” by Hy. J. 14; A. andrenaeformis, 28; A.
Turner, s go dle aliyal elegantula, 42; T. aureus, 62;
‘“Note on C. woodi,” A, by H. A. mellanarius, 63; B. lignea,
Donisthorpe, 60; from Hamp- 64; C. inquisitor, 129 ; Coleoptera,
shire, 92; on Braemar ats 159 129; D. compta, 147, 160; M. acu-
‘* Notes on the Myrmecophiles found minata, 147; T. tussilaginis, 147 ;
with Acanthomyops brunneus in A. sexpunctatus, 147; N. livida,
Britain,” by H. Donisthorpe, 121 133 148; O. titan, 148; L. brachy-
Oberthiir Collection, The .. 170 dactylus, 160; A. crataegi ab.
Obituary, Col. Swinhoe, 12; AY. H. flava, 160; EH. rufibarbis 2,
Jones, 41; C. Oberthiir, 115; Scarcity of Lepidoptera 127, 161
F. Merrifield, 93; J.H.A. Jenner, 94 | **Season in S. Hants, The,” by
Occurrence of H. urticatain U.S.A. 171 Wm. Fassnidge, 61; The . 156
Orientation among ants .. 160 | ‘‘ Seasonal Notes on ‘the Rhopalo-
Parasites in 1924, A. grossulariata cera,’’ by S. G. Castle-Russell .. 165
and.. 113 | Second generation in, D. mendica,
Pathological aberration of P. dejeanii 62 29; T.variata .. .. 166
Pest of tea-plant .. _. 14 | Societies of insects, 31; Ants 30, 42
-Phoresy of beetle and Acarid 63 | Societies : Entomological Society
Piano, Beetle pupates in and of London 13, 41, 62, 94, 130,
emerges froma .. 159 160, 171; S. London Entomo-
Polymorphism in P. polytes 147 logical Society 13, 29, 42, 64, 80,
Pupation of D. bergmanniana eeelaliss 94, 116, 129, 147, 172
Races of H. semele, 22; Table of ‘Somatic Mosaic or Mutation in
races of H. semele 22 A. grossulariata,’’ by Dr. E. A.
‘‘ Rainham Hybrids, The,” ‘by Dr. Cockayne .. 46 BB siody OME
E. A. Cockayne oe triate aberration .. ve o.
29
180
THE ENTOMOLOGIST’S RECORD.
PAGE PAGE
‘« Switzerland in 1923,”’ by D. H. variata, The” by C. Héfer 39,
Pearson Kowal 88, 119, 151, 167
Symbiosis of earwigs ‘and bats 62 Variation in, H. semele, 21; L.
Syntarus telicanus in Switzerland 10 variata, 39, 88, 119, 151; J2,
“ Taphrorychus villifrons, a species napi, 64; E.cardamines, 91; M.
of Coleoptera new to the British athalia, 94; Grypocera and Rho-
List,’’ by H. Donisthorpe . 118 palocera of Peninsular Italy, 106;
Teratological, Legs in Lepidoptera, C. arcania, 143; M. aurinia, 143,
by Dr. E. A. Cockayne, 33; R. 166; M. ismene, 148; Z. » flipen-
phlaeas, 130; Leg of A. grandis 148 dulae : 148
Time of emergence of S. pavonia.. 4 | Verrall Supper 5 29
Treitschke’s on L. variata . 153 | ‘* Wembley, Entomology ‘at, a by
Tyrrhenian area of the Mediter- HI. Moore, 157; by H. Donisthorpe 170
ranean Sea 62 | Wernerian Club -. 12
‘‘ Variation in Larentia (Thera) Young stages of Stomaphis longi
rostris : fe . 137
SUPPLEMENTS.
List of Races of the Rhopalocera of Peninsular ial by Roger Verity, M.D., and
Orazio Querct. .. ofa (2 1)- (44)
List of the Macro- lepidoptera of Hampshire and thé Isle of Wight, by Wm.
Fassnidge, M.d. .. (17)-(40)
PAGE
Locanirres :—Allos, 105, 122; Bérisal, 2 ; Basses Alps, 102; Braemar, 159;
Cleobury Mortimer, 5; Cumberland, 85; Cornwall, N.W., 142; Digne,
29, 102, 122; Hclépens, 1; Engadine, 29; Hampshire, 92; Kew, 144;
Névache-le-Chateau, 55, 139 ;
Nemours St. Pierre, 126 ; New Forest, 161;
Oxshott, 4, 20; Riviera, 29; Switzerland, 1; + Simplon, 3; Vienna, 39 ;
Wisley, 6; Windsor, 51; Wicken . 129
GT SLMOE AC ON RREBOLOERS:
PAGE PAGE
Ashby, Lt. E. B., F.E.S. 102, 122 | Hofer, C. : 39, 88, 119, 151, 167
Anderson, Jos. .. 159 | Johnson, Rev. W. F., F. E. S. . 156
Bethune- Baker, G. T., E.E. ist 10 | Kirk, Miss F. Deiat : Bou NO)
Butler, EH. A., F.E.S. : 14 | Kettlewell, H. B. D. oe 27, 156
Bagnall, R. S., F.L.S., F.E.S. 36, Leman. G. B. C., F.E.S. .. sod
58, 99 | Leman, G. C., F.H.S. Be 11, 60
Burrows, Rev. C. R. N., F.E.S. 47, Lestage, J. A. ue aa oo LEG
81, 97 | Marriner, T. F., F.E.S. 85
Burr, Dr. M., F.Z.S., F.E.S. 09) | MoorewEle He Be Ss ee 157
Cockayne, Dr. i. A., M.A.. F.E.S. Pearson, D. H., F.E.S. £4 1
6, 8, 17, 83, 149, 158 | Page, H. E., F.E.S. 16, 93
Crawley, W. C., B. A., F.K.S. 91, 160 | Pepper, H.T.C. .. .. 114
Carr, F. B. i .. 143 | Robertson, G. S., M.D 61
Castle- Russell, Ss. Gu 165 | Sich, Alfred, F.E.S. 65
Donisthorpe, H., F.Z. Si, BE. S. Smith, W. 184 F.E.S. 15
30, 42, 49, 60, 69, 92, 117, 118, Turner, Hy. Ah F.E.S., 8, 9, 10,
121, 133, 150, 170, 173 14, 27, 39, 88, 96, nae 113, 114,
Durrant, J. H., FE. S. 113 119, 127, 143, 144, 151, 167
Esson, ing Je 159 | Verity, Dr. R.. 4 21, 106
Fassnidge, Wm., M. A. 56, ‘Gi. 92, 139 | Woodward, Com. G. (. RN. 4, 20
Goodman, O. R., F.Z.S., F.E. S. 10 | Williams, H. B. A SrA OI)
Grant, F.T.. 26, 159 | Wheeler, Rev. G., F. E. Sy 127
Graves Major, P,P. _F. E.S. 90 Worssam, C. a 143
Greer, T... 91 Waldegrave, Karl. .. 143
Harrison, J. W. H., Ske, 36, 53, 99
LIST OF ILLUSTRATIONS,
Pt. I, Somatic Mosaies ..
Pt. I,
Teratological Legs in Lepidoptera ‘ c
dc. (Notiee to Binder).
to face PAGE
Lauahee pha he BS
Pt. III. &1V. Relationships of Psychides ae oe BA S6 oo! | teil
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Duplicates.—Cinxia, Bellargus, Coridon, H. Comma, Lineola, Galathea, Moneta,
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M. F. Bliss, Butlin’s Hill, Braunston, Near Rugby.
MEETINGS OF SOCIETIES.
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IMPORTANT
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BAGK VOLUMES OF
The Entomologist’s Record
and Journa! of Variation.
(Vols. I-XXXV.)
CONTENTS OF Vol. I. (Most important only mentioned.)
Genus Acronycta and its allies.—Variation of Smerinthus tiliae, 3 coloured plates—
Differentiation of Melitaea athalia, parthenie, and aurelia—The Doubleday collection—
Parthencgenesis— P#per on Taentocampidae—Phylloxera—Practical Hints (many)—
Parallel Variation in Coleoptera—Origin of Argynnis paphia var. valesina—Work for the
Winter—Temperature and Variation—Synonymic notes—Retrospect of a Lepidopterist —
for 1890—Lifehistories of Agrotis pyrophila, Epunda lichenea, Heliophobus hispidus—
Captures at light—Aberdeenshire notes, etc., ete., 360 pp.
To be obtained from—
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to whom Cheques and Postal Orders should be made payable
are
FEB
VOL. XXXVI.
Sk nC UAE
13 1925
The Entomologist’s Record & Journal of Variation.
(1924.)
INDEX.
By Hy. J. TURNER, F.E.S.
Coleoptera arranged in order of Genera.
to Soiaee with two ORAS.
ARACHNIDS.
PAGE
avellanae, Hriophyes be 37
biovata, Thyreosthenius .. 73
domesticus, Oonops.. 48
fasciata, Epeira 172
Gamasus 63
hombergi, Harpactes 138
lineatum, Theridion 148
narbonensis, Lycosa 172
Phalangidae .. 48
reniformis, Phryxus 42
COLEOPTERA.
Acanthosinus, aedilis 64
Adalia 86
obliterata .. 86
var. fumata 86
var. livida.. 86
var. sublimata .. 86
2 punctata 61, 86
10 punctata ee .. 156
**ab. lemani.. 156
Anisosticta 19 punetata 155
**ab. averbodensis .. 155
**ab, cammpinienis . 155
**ab. frenneti 156
**ab. juncorum 156
**ab. riparia. . 56 155
**ab. rubi-claustri .-- 156
**abl. schoutedeni 156
**ab. sinuata 156
**ab. simplex 156
**a6. trijuncta 155
**ab. woluwensis 156
Adonia variegata 155
**ab. bonaerti 155
Agabus melanarius .. 63
Agapanthia lineaticollis = = ‘yillogo-
viridescens oo Ws 50) UY
Agonum liveus 129
sexpunctatus 147
Aleochara sanguinea = lugubris = =
brunneipennis 50 .. 133
Anatis ocellata 86
Anisoplia floricola .. 126
Anobium 80
69
Antherophagus
The other orders arranged by Species.
Genera, Species, ete., new to Britain are marked with an asterisk, those new
——_—_—_—_—___—
| Anthribiidae. . ;
Apion aestivum = brifolii
var. ruficrus
Apoderus coryli ve
Atheta nitidula
sodalis
Attelabus curculionoides
Batrisodes adnexus .
delaportei ..
venustus °
Bembidion aeneum..
dentellum .. g
fumigatum
schiippeli ..
Boletophagus reticulata
Brachinus sclopeta .
Bruchidae
Bythinus glabratus..
Calosoma inquisitor
sycophanta
Carabus arvensis
granulatus
intricatus ..
Cassida
Cervus lucanus
Cetonia aurata é
Chilocorus bipustulatus
similis
Chlorophorus annularis
figurata
trifasciatus
Chrysomela graminis
Cicindela campestris
hybrida
Cionus scrophulariae
woodi es
Clytus arietis
mysticus
laeviuscula
verbasci
Coccidula rufa
Coccinellidae
Coccinella bipunctata
hieroglyphica
5 punctata
7 punctata
ab. lucida ..
10 punctata
122,
7
i.
11 punctata ee oe
ab. boreolittoralis.. ...
ab. cakiles.. ue o6
ab. confiuens a 40
ab. 9 punctata .. ois
Coptocephala unifasciata ..
Cosmopolites sordidus
Cryptocephalus polonicus ..
sericeus or
aureolus
frontalis
globicollis ..
Curculionidae
Dinarda :
Donacia dentipes
Dorytomus salicinus
Drusilla caniculata. .
Dytiscidae
Dytiscus circumcinetus
Endomychidae
Epipolaeus caliginosus
Erotylidae 3
Euplectus
brunneus=kunzei_ :
eG abeillei = ardeanus —
duponti .
villifrons
Kuryusa optabilis = laticollis
sinuata : 7
Kuthia formicetorum
Exochomus quadripustulatus
Exosoma lusitanica
Geotrupes vernalis ..
Godonera luperus
Grammoptera variegatus=analis. .
Halyzia conglobata ..
ocellata (Anatis) ..
14 guttata .
16 guttata..
18 guttata..
22 punctata
Hippodamia variegata
HAND
. maculigera
. subarcuata
). triangularis
ab.
arcuata
turkmenica = maculigera
7 maculata
**ab. bifasciata
ees
ADo
**ab,
bioculata At
scutellata ae aye
trifasciata
13 punctata
**ab. beffai . ye
**ab. guilleaumei ..
**ab. tonnoiri
Histeridae :
Hydaticus transversalis ..
Hypera punctata
Hyperaspis reppensis
Tlyobates glabriventris
propinquus ele O0
Lampyridae .. So G0
Larinus sternus .. de
Melanophila acuminata
, 69, 70,
SPECIAL INDEX.
95,
95,
150,
86,
86,
123,
PAGE
87
87
87
87
Leistus rufescens
Leptura cerambyciformis ..
fulva 36
Lucanus cervus ots
Melasoma populi
Micraspis 16 punctata
Microglossa gentilis. .
pulla 50
Molytes coronatus
glabratus ..
Mylabris quadripunctata
Myrmedonia limbata
Mysia oblongoguttata
Nebria livida.. :
Notothecta flavipes ..
Oedemera nobilis
podagrica ..
Onthophagus
Oodes helopioides
Opilis mollis..
Otiorhynchus sulcatus
Oxypoda formiceticola
haemorrhoa
Pachypus
Paragaeus crux- -major
Passalus
Phyllopertha horticola
Phytodecta pallida
ab. borealis
ab. nigripennis
Podabrus alpinus
Polydrusus sericeus..
Priobium castaneum
Ptenidium kraatzi -.
Pterostichus anthracinus
Ptinus subpilosus
Pyrophorus pilucidus
punctatissimus
Quedius scitus 56
Rhagium bifasciatum
indigator
Rhagonycha fulva
Rhizobius litura
Scarabaeus sacer .. 32,
Seymnus capitatus .
discoideus .
frontalis as
haemorrhoidalis ..
nigrinus
pygmaeus .
testaceus
var. scutellaris
Silpha quadripunctata
Staphylinidae
Stenichnus exilis
Subcoccinella 24 punctata..
var. saponariae
Taphrorychus bicolor
fuscus
villifrons =capronatus
Thiasophila angulata
Tillus elongatus
Trechus amplicollis. .
Trichonyx sulcicollis
69, 70,
32,
63,
126,
147, 160,
Trichopteryx montandoni .. bo
SPECIAL
PAGE
Tricodes alvearius. . .. 126
apiarius . 126
Trogophloeus corticinus .. 129
Urodon : cio be
Xantholinus glaber .. 134
Xylotrechus undulatus . 159
DIPTERA.
agilis, Endopsylla 38
Anthomyiidae 172
anthracinus, Tabanus 126
Aphiochaeta .. 136
auricomi, Perrisia WeenotG
baccarum, Rhopalomyia 36, 55
betulina, Contarinia ago
bicolor, Ocyptera 105, 126
bombylans, Volucella .. 126
Bombylius on Oe)
bovinus, Tabanus . 105, 122
brachyptera, Peyerimhoffia sere)
brasiliensis, Dohrniphora .. 12
brevipalpis, Glossina 157
bromius, Tabanus .. 126
calamagrostidis, Mayetiola 37
cautum, Chrysotoxum ‘ -. 105
Cecidomyiidae g iG. 53, 99
cerealis, Prolasioptera se) exe
ciliata, Aphiochaeta 70, 136
clethricola, Jaapiella SH RONG
cornifex, Hormomyia ‘ 38
coryligallarum, Arthrocnodax . 37
crassimana, Limosina 70, 136
cruciatus, Bombylius Se NG
cucubali, Contarinia 55
curtiventris, Limosina go UO)
Deuterophlebia (iidae) 95, 145
devius, Microdon iaylia
diadema, Selidopogon 122, 126
donisthorpei, Pay eMy 2 71
Drosophila Peis)
eggeri, Microdon . : COS ee
elegantula, Agathomyia |. bby 9 (42
Empidae : : 172
eriophori, Stenospatha .. 36
fagi, Contarinia 36, 38
ferox, Fabricia 35 Ie
flexuosa, Lasioptera 53
floriperda, Jaapiella 55
formicae, Phyllomyza val
fraxinea, Perrisia o4
frireni, Hormomyia 38
fungicola, Limosina 79
gallarum, Dichrona 38
geniculati, Stenodiplosis .. 53
glaucius, Syrphus .. sre .. 126
globuli, Harmandia.. ah oy row
gracilis, Amerhapha C0 38
holci, Mayetiola 37
Hyperechia .. -94, 96, 145
inanis, Volucella 126
inflatae, Jaapiella . on .. 55
juncorum, Livia .. 5c sgss
kneucheri, Hormomyia 38
lanceolatae, Mayetiola 37
INDEX. iii.
PAGE
lasiae, Phyllomyza .. j 71
| latefasciatus, Syrphus .. 124
| latifrons, Microdon . Tile Ue
lathyri, Asphondylia we (5 0
Limosina : 3 70
liviae, Lestodiplosis 38
longipennis, Glossina sta 157
manicatus, Platychirus 126
micans, Pangonia .. ne ie L126
mosellana (aurantiaria), Sitodi-
plosis 5 6 : ¥ coy BR
Mycodiplosis. . . 99, 100, 101, 102
myosotidis, Perrisia 3 oo BE
oculiperda, Rhabdophaga .. 37
oelandica, Dioctria .. : 126
ornata (micans ab.), Pangonia 126
ornatum, Xanthogramma.. 126
palpalis, Glossina 157
pellucens, Volucella 105
Phoridae aS 12
phragmitis, Porricondyla bs .. 58
Phyllomyza .. : 10; Gl
pimpinellae, Schizomyia 38
pipiens, Syritta 126
pisi, Contarinia 36
pisi, Diplosis 38
plumata (bombylans ab. ); Volucella 126
populnea, Lasioptera oe ake
pustulans, Harmandia 36
| quator-notatus, Tabanus .. 103
rhenanus, Microdon 72
ribesii, Syrphus 126
rudis, Hrigone bb 126
rufibarbis, Eutolmus 172
ruficornis, Cyrtopogon 105
rufilabris, Limosina soup
sabaudus, Stenopogon 124, 126
Schizomyia .. . 388
| schlechtendaliana, Contarinia 38
| securicornis, Phyllomyza .. 71
similis, Perrisia 50
socialis, Perrisia 37
subterranea, Perrisia 37
subterranea, Peyerimhoffia | 73
Tabanidae .. 158
tanaceticola, Clinorrhyncha 36
tessellata, Empis c 105
tremulae, Harmandia 37
tuberifica, Hormomyia 38
tussilaginis, Trypeta 147
valerii, Rhopalomyia 55
variabilis, Bombylius 123
variabilis, Chilosia .. 105
veronicae, Jaapiella 55
vitripennis, Syrphps 122
zonaria, Volucella .. 126
HYMENOPTERA.
abdominalis, Camponotus.. -. 53
Acanthomyops 5 ee lid, Jiss,
acervorum, Leptothorax one ce tt
Aenictus : 30 .. 174
aestuans, Xylocopa.. 131, 145
albiseetus, Halictus. -. 126
iv. SPECIAL INDEX.
PAGE
alienus, aan Tee: 51, 70, 73, 122
Allodape ue 0 43
amydei, Humenes .. 125
Annoma .. 174
Apidae, Apis.. , 31, 48
arcuatus, Allantus 60 .. 105
arenaria, Cerceris .. 126
Atta, Attini .. : S6 Uress. abzé!
bayeri, Camponotus ~ AeA cio ll
Bombus . 30 .. 43
bombycinus, Cataglyphis AN . 163
brachialis, Synacra.. ee pealtaG
brevicorne, Exochilium . 126
brunneatus, Camponotus
brunneus, Acantbomyops, Lasius
50, 51, 70, 73, 117, 121, 122, 133,
134, 135, 136, 137, 188, 171, 174
burmeisteri (nigricans race),
Dorylus.. 90 -. 64
caespitum, i etramoriun an 70, 174
Camponotus (inae) . hi 91, 175
Cataglyphis .. oo aly
Cataulacini .. 94 . 175
centuncularis, Megachile .. 148
Cerapachyinae (ini).. .. 44, 176
Chalcididae .. ‘ bo a 62
chrysosceles, Andrena O° Sls}
coarctata, Ponera ..49, 70, 176
Colobopsis 175, 176
Conostigmus. . : a -. 136
crassitarsis, Pedanaspis As 59) dle
Cremastogasterinae (ini) 173, 174, 176
cruentatus, Camponotus .. .. 125
Cryptocerinae (ini) .. 125, 175, 176
cylindricus, Halictus 125, 126
Dacetini oe o0 175, 176
didonis (salomonis var.), Mono-
morium A a0 55 G83
Dolicoderinae 4 44
Dorylus (inae) . 44, 158, 173, 174
dubiosus, Conostigmus 136
Kciton ‘ .. 174
eduarduli, Cryptocerus oo. les
elongata, Leptogenys . 176
emarginatus, Lasius . 174
Epiponinae .. o6 a0 st 43
exsecta, Formica 70, 133
extensorius, Ichneumon 0 hs)
flavifrons, Scolia ‘ae 164
flavus, Acanthomyops 51, 69, 70,
3, 74, 133
foraminosus, Camponotus.. Gi]
Formicidae (inae) 44, 49, 50, 121, 175
fuliginosus, Acanthomyops 50, 51,
52, 63, 70, 71, 73, -74, 121, 133,
134, 185, 186, 137, 174
fulvus, Dorylus 6 174
fusca, Formica 49, 70, 71, "23, 74,
75, 125, 136
gallica, Polistes a 22125
Gigantiops (Gigantrops) 162, 177
glebaria (fusca race), Formica .. 70
graminicola, Myrmecina .. oc.) 4)
grandis, Leucaspis .. 62, 125
Halcomyrmex AG een CAVA S
PAGE
Halictus ..43, 44, 96
hattorfiana, Andrena ¢ .. 103
herculeanus, Camponotus .. SORTS
Ichneumonidae z Sa . 157
ichneumonoides, Methoca .. .. 130
innotatus, Conostigmus . 136
instigator, Pimpla .. oi .. 125
laevinodis, Myrmica ..-50, 69, 70
Leptanillini ms é s .. 174
manicatum, Anthidium 123, 124, 125
marthae, Trachymyrmex a .. 174
Messor é E .. 162, 174
melanaria, Sphex 103, 104, 124
Melipona (inae) .. .. 48, 44
mixtus,Acanthomyops 50, 52, 122
molesta (nigricans ab.), Dorylus .. 64
monostagon, Melanichneumon .. 124
muraria, Chalicodonia .. 105, 122
Myrmica (inae) 44, 49, 69, 135, 161,
174, 175, 176
Myrmecia .. 176
niger, Acanthomyops 50, 51, 69, 70,
72, 73, 122, 138, 136
nigeriensis (perrisii race), Cam:
ponotus .-91, 92, 170
nigricans, Dorylus .. Ho .. 64
nitidulus, Halictus .. .. 125
nylanderi, aes es 50, 122
Oecophylla «. 175
olivacea, Allantus 122
orientalis, Dorylus .. 174
palliatorius, Amblyteles 125
pallidula, Pheidole .. i74
paniscus, Ophion Gi 125
pectoralis, Glyptomorpha .. .. 125
perrisii, Camponotus EGO a0
pharaonis, Monomorium .. .. 49
Pheidole We 173, ots 176
Pheidologeton We a 174
Platygasterinae 146
Pogonomyrmex 146, 174, 175
Polistes (inae) G0 o. 43
Polyrhachis .. 96 Sic e. 175
pomiiformis, Humenes .. .. 125
Ponera (inae) .. 44, 49, 173, 176
Proctotrupidae 136
Pseudomyrminae (ini) 44, “45, 178, 176
Pseudomyrmex é 162
Psithyrus . 43
quadrimaculata, Anthophora . 124
quadripunctata, Discolia 122, 125
Rhagomyrmicinae . 173, 176
Rhopalidiinae 43
rufa, Formica 52, 69, 70, ‘71. 73,
138, 135, 136
rufahirta, Osmia .. vy 25
rufiventris, Acropiestra .. -. 136
ruginodis, Formica... 69, 70
rugulosa, Myrmica .. .. 69
rupestris, Psithyrus.. c .. 123
sabuleti (scabrinodisvar.), Myrmica 50
sabulosa, Ammophila .. 124
salomonis, Monomorium .. 163
sanguinea, Formica 52, 70, 71, 133,
135, 136
SPECIAL INDEX.
PAGE
sanguinea, Myrmecia te .. 176
scabiosae (zebrus), Halictus . 125
scabrinodis, Myrmica 49, 50, 70, 133
sexcinctus, Halictus 124, 125
singulatus, Stronygaster . 125
smaragdina, Formica te She
Solenopsis . 174
Sphecidae Bil
striolata, Acropiesta . 136
Strumigenys .. ; . 176
sulcinodis, Myrmica 50 CW)
sylvestris, Vespa .. 126
thoracicus, Camponotus . 164
Trigona ve fe «- 48
truncatus, Camponotus .. L715
umbratus, Acanthomyops.. 50, 122
urnarius, Sphex .. te .. 43
vagus, Crabro . 147
varians, Andrena .. 125
Vespa (inae) i Slaw
vestalis, Psithyrus .. -. 124
viatica, Ammophila, Sphex 108, 123
xanthorius, Ichneumon 122, 126
zebrus = scabiosae .. 125
zonulus, Halictus alos
ISOPTERA.
Mastotermitidae .. 6 46
Mesotermitidae on O6 46
Metatermitidae 46
Protermitidae WwOHIAG
Termitidae 32, 46
LEPIDOPTERA.
abbreviata, Kupithecia 61
abietaria, Boarmia .. a 26
abruptaria, Hemerophila . 61
absinthii, Cucullia .. 141
aceris, Acronicta, Avaielatri 76
Acidaliinae : 77
achilleae, Zygaena 103, 105, 125,
140, 148
Acraea -. 48
Acronyctinae 76
actaea, Satyrus 124
acteon, Thymelicus.. 105
Adela.. 00 83, 84
addenda (jurtina ab.), Epinephele
29, 30
adippe =cydippe 123, 139, 165
admetus, Polyommatus, Hirsutina
103, 104, 123, 124
adonis = thetis ag 7
adusta, Eumichtis, aden 716
advena, Aplecta 76
pavonaninl Epione ue eA
aegeria, Pararge 1, 30, 116, 142
Aegeriidae .. 78
aegon=aregus 6, 14, 20, 30, 105, 122,
125, 140
aesculi=pyrina . 78
aestiva (duponcheli a. gen), Lep-
tosia ae ae .. 123, 124
v.
PAGE
aestiva (medon a. gen.), edaae
Aricia a po ade)
affinis, Calymnia 77
agathina, Agrotis 76
agavus, Papilio . 12
aglaia, Argynnis 20, “5, 139, 142,
159, 165
agrippina, qyeaae 94
Agrotinae .. : D0 So) abel
ain, Plusia .. a0 141
nibicomelle: Tinea .. 63
albipuncta, Leucania : .. 140
albonigrata Verae ab.), Larentia,
Thera 6 88, 152
albulata, Perizoma . BS oO
albulus (delphius race), Parnassius 147
alceae, Erynnis 106, 125, 140
alchemillata, Perizoma . .. 142
alciphron, Heodes 3, 104, 105, 123, 140
aleon, Lycaena 2, 124
aleyone (fagi), Satyrus, Nytha .. 124
alecto, Erebia ae 29, 106
alexanor, Papilio 102, 104, 105
alexis =icarus ae Sa Svean |
algae, Bryophila 140
algirica (semele race), Hipparchia
24,25, 26
alopecurus (rurea ab.), Xylo-
phasia ae y an HR (3
Mr aeeealist Orenaia.. 141
alpestris, Agrotis .. a6 .. 140
alpina (comma race), Urbicola 107, 108
alpina (didyma race), Melitaea 123, 139
alpina (medon race), Plebeius, Aricia 140
alpina =hyperborea.. : .. 159
alpinalis, Scopula 30 .. 141
alsoides (minimus race), Cupido . 2
alternana (straminea ab.), Con-
chylis, Huxanthis .. 141
altheae, EKrynnis .. 106, 125
| alveus, Hesperia 57, 105, 140
amata, Timandra 5, 6, 142
amuathusia, Brenthis .. 139
ambigua, Caradrina 140
ambrizia, Anaphe 158
Amicta 98
ampliatella, Phycis 141
Anaphe o¢ : 158
anceps =sordida 76
ancilla, Naclia 66 oe .. 125
andereggii, Leucania 140
andrenaeformis, Aegeria 28
**angliae (semele race), Hipparchia 22
**anclorum (semele race), Hip-
parchia ae So 2
annulata, Ephyra .. a big!
anthedon (dubia var.), Hypelimnne 14
anthyllidis, Zygaena 33
antiopa, Huvanessa 58, 75, 139, 167
antiqua, Orgyia 82, 84
apennina (comma race), Urbicola
107, 108
apenninicola (argus race), Plebeius 110
apenninigena (semele mee ae
parchia : : . 26
vi.
PAGE
apiciaria, Epione -. 78, 141
apiformis, Trochilium ae 1, 140
apollo, Parnassius 33, 57, 103, 105,
125, 139
applanella, Depressaria .. 141
aptata, Calostigia pl ajo) Jul
arbusculae (lanestrisrace), Lachneis 140
arcania, Coenonympha 2, 103, 105,
124, 139, 143
arcuosa, Petilampa.. 50 Oy AOE 7
Arctiidae (inae) i ao AG
areola, Xylocampa .. 92
argentana, Huxanthis .. 141
argiades, Kveres 125, 140
argiolus (Lycaenopsis), Cyaniris 4,
59, 140, 172
argus (aegon), Plebeius 6, 14, 20, 30,
105, 110, 122, 125, 140
argus=argyrognomon 103, 105, 140
argyrognomon, Plebeius 59, 103,
105, 123, 140
arion, Lycaena 2, 108, 130, 140, 142
aristaeus (semele race), Hipparchia
21 2224 25426
aristolochiae, Papilio . 147
armoricanus, Hesperia 107
artemisiae, Cucullia 141
artesiaria, Diastictis : 141
arundinis (typhae), Nonagria 77
artaxerxes (medon mak Plebeius,
Aricia b0 oe Ja!)
asella, Heterogynis .. od | Sy: es)
asiliformis (cynipiformis), Aegeria
78, 125
assimilata, Hupithecia .. .. 148
astrarche—medon . 103, 140, 160
atalanta, Pyrameis 21, 29, 42, 58,
139, 143, 144, 167
athalia, Melitaea 2, 94, 103, 142
athamanthae (ephialtes ab.), Zy-
gaena .. Ba Sod EES 110453
atomaria, Ematurga, Fidonia 4,6, 35
atrata, Odezia ate a seo diel
atropos, Manduca .. 76, 148, 156, 159
augur, Agrotis, Noctua ae .. 140
**aurata (comma race), Urbicola
107, 108
aurata, Pyralis -. 141
aureus, Teinopalpus : bo, OZ
aurimaculatus (agavus ab.), Papilio 12
aurinia, Melitaea 2, 29, 30, 75, 116,
139, 142, 143, 166
aurita, Setina 125, 126, 140
auroraria =muricata ae ao UU
ausonia (crameri race), Anthocharis
29, 90
australiformis (altheae race), Hryn-
nis .. le .. 106
australpina (arion race), Lycaena.. 109
australis (alceae race), Erynnis 106
autumnaria (ata), Epirrita 30, 42
aversata, Acidalia .. Bie 6, 142
badiata, Anticlea 5
baja, Noctua.. we 20
bajularia = pustulata 64
SPECIAL INDEX.
PAGE
ballus, Thestor, Tomares .. 29
bammakoo, Elymniopsis .. ar ytd
belemia, Anthocharis 129,. 147
belia =ausonia eo
belia =eupheno ae oa dl2t)
bellargus=thetis .. O60 Oy
berberata, Anticlea . ee .. 141
bergmanniana, Dictyopteryx 113, 129
betulae, Ruralis 75, 140
betularia, Amphidasis 141, 171
bicolorata, Mesoleuca 78, 142
bicoloria, Miana .. 142
bidentata, Gonodontis os 5
bifasciata (unifasciata), Perizoma
158, 159
bilineata, Camptogramma.. 5
bipunctaria; Eubolia, Ortholitha
20, 141, 142
birivia, Agrotis ae .. 141
bivittata (sinapis ab.), Leptosia 111
blachieri (semele ab.), Hipparchia
eG
Boarmiinae . ; oo. ths)
boeticus, Lampides .. 3, 59, 140
bolandii (urticae ab.), Aglais 167
boleti, Scardia : 80
brachydactyla, Leioptilus, Pselno-
phorus : 160
brassicae, Pieris 20, 21, 139, 144, 171
brassicae, Mamestra 142
Brassolinae QO MB
brassolis, Liphyra 160
briseis, Satyrus 139
brunnea, Noctua ie ara O
brunneata, Halia 57, 141, 159
bucephala, Phalera.. 6 .. 148
cacaliae, Hesperia .. as -. 106
cadmus (semele race), Hipparchia
22, 23, 24, 25, 26
caesia, Dianthoecia. . , 141
caesiata, Entephria, Larentia 5 Zul
caja, Arctia ae : .30, 42, 148
calabrica (argus race), Plebeius 110
c-album, Polygonia. . ae 21, 139
calida (medon race), Plebeius,
Aricia o¢ .. 109
callidice, Pontia . 139
calodactyla, Platyptilia 141
camelina, Lophopteryx .. 140
camilla =rivularis 2, 59, 105, 127, 139
candidata, Asthena.. 141
candidum (cribrum ab.), Coscinia,
Emydia Boi Oi ote .. 140
caniola, Lithosia ~~. 125, 140
capsincola, Dianthoecia .. 141
capsophila (carpophaga a Dian-
thoecia .. 76
cardamines, Euchloé 4, : 28, 30,
; 91, 139
cardui, Pyrameis oe 123, 139
carlinae, Hesperia .. 2
carmelita, Odontosia, Lophopteryx 76
carniolica, Zygaena 38, 105, 124, 140
carpophaga, Dianthoecia .. 76
carthami, Hesperia.. - 125
PECIAL INDEX.
PAGE
cassandra (polyxena race), ss
Zerynthia .. 29
cassiope (epiphron race), Erebia .. 139
castigata, Hupithecia ube 5, 98
castrensis, Malacosoma 123, 140
catilla, Catopsilia no Gh)
caulotosticta (cardamines ab.),
Kuchloé .. aie ao sy ee GML
cecropia, Samia et ENG)
celtis, Libythea ae .. 104
cembrae (variata race), Thera, Lar-
entia te , Al
centaureae, Hesperia 6 -- 96
centripuncta (tiliae ab.), Mimas .. 19
cerago=fulvago .. ae .. 129
cerri (ilicis ab.), Strymon .. 105, 125
cervinata, Ortholitha 77, 142
cerymica, Ploetzia .. sa OG
cespitis, Luperina on soy
ceto, Hrebia .. art aa 2, 122
chaonia, Drymonia.. 61, 76
chenopodii=trifolii. . .. 141
christi, Hrebia 2,3, 30
christyi, Epirrita 36 a5) 30)
chrysitis, Plusia .. as 6, 148
chrysorrhoea (similis), Nygmia 20
chrysozona, Hecatera, Hadena 141
cicatricalis, Nola 140
cinctaria, Boarmia .. 92
cinerea, Agrotis 142
cinnus (coridon ab.), Polyom-
matus 5 ae 30
cinxia, Melitaea 59, 139
circe, Satyrus 5 : 103, 123
circe (dorilis ub.), Heodes.. 108
cirsii = fritillum ae 140
citrata (Immanata), Dysstroma 141
clavipalpis (cubicularis), Atheta,
Caradrina . 55 .. 141
cleodoxa (cydippe ab. i Argynnis.. 29
cleopatra, Gonepteryx 108, 123, 125
Cochliopodidae ae 46. GY
cognata, Thera, Larentia .. 141
Colias 3 : 149
comes (orbona), Triphaena -. 20
comma, Urbicola 107, 140
complana, Lithosia .. 140
compta, Dianthoecia 147, 160
confusa (lis), Nola 27, 92
congregarius, Diapalpus .. .. 158
coniferata (variata ab.), Thera,
Larentia iets ; .. 42
conigera, Leucania .. .. 140, 142
conjuncta (filipendulae ab.),
Zygaena 50 Barred 10)
consonaria, Boarmia sls aa) BH
convolvuli, Agrias .-59, 76, 140
coracina, Psodos ae . 141
cordula, Satyrus Bo .. 103
coridon, Polyommatus, Agriades
2, 20, 29, 30, 75, 80, 116, 126, 140,
148, 160, 165, 166, 173
coronata, Kupithecia ok 56) SE
coronilla (ephialtes ab.), Zygaena 3
corticea, Agrotis 6 .. 142
vii.
PAGE
corylata, Cidaria ... re 5, 89
Cosmophila .. Ao -- 95, 145
Cossidae ; 55 (hs
costaestrigalis, Hypenodes. . 17
costalis, Pyralis -. 125
**costimaculata (variata. ab.),
Thera, Larentia .. 89, 152
cotswoldensis (arion race), Lycaena 108
eraccae, Toxocampa .. 141
crameri, Anthocharis 29, 139
crataegana, Tortrix . ay .. 141
crataegi, Aporia 105, 139, 160
crepuscularia, Tephrosia sevana ye
cribrum, Coscinia .. 140
cristana, Peronea 92, 96
crocale, Catopsilia . 95, 131
croceago, Xantholeuca Sah BA
crocealis, Kbulea 141
eroceus, Colias 139
cubicularis=clavipalpis .. 141
culiciformis, Aegeria 61, 78
cultraria, Drepana .. 82, 83
cuprea, Agrotis 56 .. 141
curtisana (cristana ab.), Peronea .. 96
curtula, Pygaera 61
cyanata, Entephria, Cidaria 141
cydippe (adippe), Argynnis 29, 123,
139, 165
cynipiformis = asiliformis = vespi-
formis : sc aS as
cynthia, Melitaea .. Fas 2, 139
cynthia, Philosamia 146
cytherea=matura .. SOE Teco Path
damon, Polyommatus, Hirsutina
57, 105, 124, 140
dan, Coladenia a rite)
daphne, Brenthis .. 104
daplidice, Pontia . ey el 2 Grelt39
dardanus, Papilio 14, 95, 132, 157,
170, 172
darwiniana (arecania race), Coeno-
nympha 2, 105, 143
davus, Coenonympha 159
debilis (aurinia var.), Melitaea 139, 143
decolorata =flavofasciata .. 5, 142
decora, Agrotis ae .. 141
defoliaria, _EHrannis, Hybernia,
Larentia .. Sie cis 30, 35
dejeanii, Pyrameis .. 62, 80
Delias : Fi 116, 132
delius, Parnassius oo ee)
delphius, Parnassius 147
dentalis, Odontia Ans -. 141
dentina=nana sie . 9, 141, 143
deplana, Lithosia 5 76, 140
depuncta, Noctua, Agrotis .. . 141
derasa, Habrosyne ..-.. .. 142
deserticola (sinapis race), eee Tle
designata, Ochyria .. 5
detersa, Rhizogramma .. 141
dictynna, Melitaea 2, 29, 30, 57, 139
dictaeoides, Phaeosia ae 76, 144
didyma, Melitaea .. 59, 104, 123,
139, 148
didymata, Melenydris, Larentia .. 141
viii.
PAGE
diffinis, Calymnia .. ole ou Oe
diffusa (semele var.), Hipparchia.. 25
dilucida, Spintherops é -. 141
dimidiata, Ptychopoda, Acidalia .. 142
diniensis (sinapis race), Leptosia.. 111
dilutata, Epirrita ue 42
discobolus, Parnassius 147
dispar, Ocneria, Lymantria . 33
dissoluta (sertata var.), Acasis,
Lobophora. . 89
dissoluta (stragularia ab.), “Thera,
Larentia : 3 152
dissoluta (variata ab.), “Thera,
Larentia a oc. Sy
distinctaria, Eupithecia Nana
divisa (juniperata ab.), Thera,
Larentia Ae te sists)
divisa (variataab.), Thera, Larentia 89
dodoneata, Eupithecia oo BE
dohertyi (marshalli race), Mima-
craea oo bd 66 .. 145
donzelii, Plebeius, Aricia 29, 57,
123, 140
dorilis, Heodes, Loweia 108, 124,
126, 140
dorus, Coenonympha, 103, 125
doubledayaria (betularia ab.),
Biston, Pachys, Amphidasis 171
dryas, Enodia, Satyrus 123, 124
dubia, Hypolimnas .. wi 14
dubitata, Triphosa .. an real:
duponcheli, Leptosia .29, 123, 124
efformata, Anaitis 30, 42, 64, 77, 147
egea, Polygonia 125
elegans, Rhyacia 141
eleus (phlaeas race), Rumicia.
Heodes 4 125, 140
elinguaria, Crocallis 20, 141
elongata, (napi ab.), Pieris a. dlzal
elpenor, Kumorpha. . 76, 147
eltola, Suastus Ata)
elutata =furcata 78
emarginata, Ania, Acidalia 6
Endromidae : eG
engadinensis (andereggii race),
Leucania .. dt Ao .. 140
ephialtes, Zygaena .. ..8, 124, 125
epiphron, Erebia ae 122, 139
Krebia 35 ay
eris (niobe var. ); Argynnis. . 122, 139
eros, Polyommatus.. 123, 140
erosaria, Ennomos .. 78
Hrycinidae de a 157
erynnis (gorge ab.), Hrebia 139
escheri, Polyommatus 2, 103, 123,
124, 125, 140
eumedon, Polyommatus, Aricia
106, 140
eupheno (belia), Anthocharis 129
euphenoides, Huchloé 59, 139
euphorbiae, Hyles, Deilephila 59,
103, 104, 140
euphorbiae, Pharetra 140
euphrosyne, Brenthis 4, 5, 8, 27, 30,
49, 139, 165
SPECIAL INDEX.
| PAGE
| Eupithecia 147
europomene (palaeno “race), Colias 139
| euryale, Hrebia ok -. 105, 139
eurybia (hippothoé ab.), Heodes .. 140
Kusphalera .. a GO,
exanthemata, Cabera tag
exclamationis, Agrotis 80, 142
| exigua, Laphyema 3a 58, 125, 140
exulans, Zygaena .. 3, 58, 140, 159
exulis, Crymodes 141
falcula (falcataria), Drepana 20,
143, 148
falloui, Anthocharis by WEDS:
fascelina, Dasychira ..27, 58, 140
fasciaria, Ellopia 154, 167, 168
fasciata, Labanda RS 3095
fasciuncula, Miana .. Ae 5, 142
fausta, Zygaena 105, 124, 140
febretta, Amicta ve 98, 99
fenestrella, Thyris . .. 125
ferschaultella, Luffia LEI 9,
festucae, Plusia 141, 156
fidia, Satyrus 105, 123, 124
filipendulae, Zygaena 3, 6, 20, 30,
82, 84, 103, 130, 140, 147, 148
fimbria, Triphaena .. Be 6, 20
firmata, Thera, Larentia 168, 169
flava (linea, thaumas), Adopaea 6,
125, 140, 142
flava (comma ab.), Urbicola 108
flava (crataegi ab.), Aporia.. 160
flava (napi ab.), Pieris 6 .. 64
' flaveolaria, Ptychopoda, Acidalia
| 106, 141
| flavescens (fulvago ab.), Citria 140
| flavescens (napi ab.), Pieris 64
| flavicinctata, Cidaria, Larentia 141
flavicornis, Polyploca 61
flavicincta, Polia ane po MOL
flavofasciata (decolorata), Perizoma
, 142
florella, Depressaria at .. 141
fluctuata, Xanthorhoé .. 5, 14, 120
| fluctuosa, Palimpsestis 76
fowleri (coridon ab.), Polyommatus 166
fraxinata, Hupithecia 66) 23
fraxini, Catocala hs 141
fritillum (cirsii), Hesperia .. .. 140
fuciformis, Hemaris 4 5, 147
fuliginosa, Phragmatobia .. 6 18)
fulva, Tapinostola .. 77
fulvago (cerago), Citria 21, "99, 129, 140
| fulvata (Cidaria), Larentia 141
fulvipinnulis (altheae ab.), Erynnis 106
fumata (ternata), Pylarge, Acidalia 77
funesta, Aedia 125
furcata (sordida, elutata), " Hydrio-
mena a at 6, 20, 78, 141
furcatellus, Crambus else
furvata, Gnophos 125
fusca, Phycis 141
fusca, Pygmaena : 106
galathea, Melanargia 13, 123, 124,
126, 139, 142
gallica (medon race), Plebeius, Aricia 109
SPECIAL INDEX.
PAGE
gamma, Plusia . 6, 20, 141
gemina, Apamea, Hadena.. 141
gemmaria=rhomboidaria . 80
genistae, Mamestra, Hadena by
Geometridae. . .. 77, 132, 141, 143
geryon, Adscita 140
glabraria =jubata 1.50, 93, 142
glareosa, Noctua 76
glauca, Mamestra, Hadena 141
glauce (belemia race), Anthocharis
glaucinaria, Gaeplies
enaphalii, Cucullia . 77, 147
goante, Krebia ihe 2, 139
gordius (alciphron race), Heodes 3,
104, 105, 123, 140
gorge, Hrebia eel 22139
graeca (ausonia race), Anthocharis 90
grandipennis, Butalis .. 129
grandis, Lohita a 172
grandis (sinapis race), Leptosia 111
erisealis, Zanclognatha .. 20
**griseofulva (alceae race), nee 106
grisescens, Agrotis .. .. 141
grisescens, (stragulata ab.), Thera 152
erossulariata, Abraxas 5, 17, 18,
19, 29, 42, 113, 141
gueneci, Apamea .. ae .. 143
halterata (hexapterata), Lobophora 92
hastata, Hulype .. We SS)
hastiana, Peronea .. ok .. 94
hector, Papilio .. 147
hectus, Hepialus wi SEAS
helice (croceus ab.), Colias 139
heliconia, Asota .. ae 96
helvola (rufina), Amathes .. . 140
Hepialus 2° 83, 85
hera = quadripunctaria 124
hermione=mayjor, Satyrus, Nytha 103
herminiata, Diplodoma .. 99
Hesperia (idae) 9, 96, 107, 109, 145
Heterocera 140
Heterogynis .. 82, 84
hexapterata = haltera. Be su Be
hiberna (semele race), Hipparchia 26
hippocastanaria, Pachyenemia 6
hippocoon (dardanus race), Papilio 14
hippomene, Antanartia .. 64
hippothoé, Heodes .. ats .. 140
hirtaria, Lycia 33, 35, 61, 128, 149
hispidaria, Apocheima 29, 33, 34,
35, 61
hispulla (jurtina race), Epinephele 29
bochenwarthi, Plusia 5 .. 141
hospita (plantaginis race), Nemeo-
phila, Parasemia. . at .. 140
hyale, Colias y 75, 139
hyalinalis, Botys so eh
hybridalis = noctuella 125, 141
Hydriomeninae Sion UU
hylaeiformis, Bembecia .. .. 140
hylas, Polyommatus 2, 103, 116, 140
Hypeninae UU
hyperantus, Aphantopus 6, 42, 142, 165
hyperborea, Agrotis, Pachnobia .. 159
icarinus (icarus ab.), Polyommatus 29
ix.
PAGE
icarus, Polyommatus 5, 7, 21, 29,
105, 123, 140, 142, 148, 166
ichneumoniformis, Aegeria 140
ilicis, Strymon, Nordmannia 103,
104, 105, 125
imitaria, Acidalia, Leptomeris 142
immanata=citrata .. o5 .. 141
immorata, Leptomeris, Acidalia
141, 148
immutata. Leptomeris, Acidalia .. 77
imperialis, Teinopalpus 130
impudens (pudorina), Leucania 77
impura, Leucania .. .. 6, 20, 125
incanaria = virgularia = seriata, Aci-
dalia, Ptychopoda .. 141
Incurvaria 83, 84
iners (suspecta), Dyschorista 77
infraplumbea (medonab.), Plebeius,
Aricia . 50 .. 109
infuscata (furcata ab.), Hydriomena 6
ino, Brenthis & a 22139
insulata (variata ab.), Larentia,
Thera oD bi so° tel
insulata (silaceata ab.), Larentia 89
interjecta, Triphaena ps .. 20
interrupta (corylata ab.), Cidaria.. 89
interrupta (sagittata ab.), Cidaria 89
interrupta (stragulata ab.), Larentia
Thera a0 a .. 152
interrupta (variata a Larentia,
Thera ae 89
io, Vanessa 20, 21, ‘58, 139, 143,
144, 148
iota, Plusia .. 33
iphis, Coenonympha, 105, 122
irriguata, Hupithecia ang
ismene (leda), Melanitis 148
**italaveris (dorilis race), Heodes 108
italorum (dorilis race), Heodes 108
jacobaeae, Hipocrita ne 6, 148
janthina, Triphaena Ne .. 20
jubaris (semele race), Hipparchia
22, 23, 25, 26
jubata (glabraria), Cleora ..30, 93, 142
juniperata, Thera, Larentia so. Sy)
jurtina, Epinephele 5, 6, 20, 29, 30,
116, 142, 165
lactearia, Iodis S 5
lacticolor (grossulariata ab.),
Abraxas .. HK soll, ash 118)
laius, Libythea : .. 63
lamborni, Aslauga .. FAA .. 160
lanceolata (hyperantus ab.),
Aphantopus ae .. 165
lanestris, Lachneis .. 140
lapidella, Luffia 30. 0h)
lappona, Hrebia 2, 30
lapponaria, Ithysia.. .. 149
Larentia : .. 39
lariciata, upitheeia: 93, 141
Larinopoda 50 ° .. (14
latelians (galathea race), Melan-
argia i ae : 56, HAG
lateritia, Hadena .. 141
lathonia, Issoria 126, 139
x SPECIAL INDEX.
PAGE PAGE
lathyri (sinapis race), Hepeoee .. 111 | machaon, Papilio 105, 125, 126,129,
laura, Castnia 5 12 130, 139
lavaterae, Hrynnis .. by 125, 140 | macularia, Venilia.. . 5, 106, 129
leda =ismene ah 5 148 | maculata (rivata ab.), Larentia,
leopoldella, Tinea .. is 84, 113 Xanthorhoé 3 ts $5) tk)
leporina, Acronicta .. 143, 144, 148 | maculata (variata ab. ), Larentia,
leucographa, Pachnobia .. aie itil Thera ae Bo. tek)
leucomelas (galathea ab.), Melan- maderensis (semele race), Hippar-
argia 4 3, 123, 124 chia : ; aH Aon) 213)
leucostigma (secalis ‘ab. ),Apamea.. 20 | maera, Pararge 103, 124, 139
libatrix, Gonoptera .. é' 5, 142 | magna (sinapis ab.), Leptosia 111
lichenaria, Cleora 3 78 | **magnaustralis (alceae race),
licus, Castnia 12 Erynnis : df; .. 106
lidderdalii, Armandia 130 | malvae, Hesperia .. 4,5, 6, 125, 142
ligea, Erebia.. 124 | manni, Pieris ae .. 125
lignata (vittata), ‘Phibalapteryx, margaritaria, Metrocampa, Cam-
Orthonama 78 paea fs sas
lignea, Blastobasis .. 64 | margaritosa (saucia ‘ab. ), Peridroma
lignicolor, Gnophos.. 125 76, 141
ligula (spadicea), Cerastis, Orrhodia 116 | marginata, Ania .. 141
ligustri, Sphinx .. oh 13, 64 | marginata, Lomaspilis 141
Limacodidae. . : 2 .. 83 | marginata=umbyra . 77
limitata (mensuraria), EKubolia, marginaria, Hybernia 64
Ortholitha 20, 141, 142 | marginea, Catastia . ah spp nll4ili
lineola, Adopaea .103, 125, 126, 140 | marginepunctata (promutata), Aci-
linguliformella, Adela 84 dalia, (Leptomeris) : .. 141
Liparis (idae) 82, 83 marshalli, Mimacraea : 145
Thiphyrinae .. 160 | maxima (ausonia g.Q.), Anthocharis 90
literana, Leptogramma .. 92 | matura (cytherea), Cerigo .. <1
literosa, Miana 76, 142 | maturna, Melitaea .. 35
lithargyria, Leucania 20, 142 | maura, Mania ‘ ag Sp 240)
Lithosiidae .. BG -- 76 | maurella, Lypusa .. ab 82, 83
lithoxylea, Xylophasia 125, 142 | medon (astrarche), Plebeius,
littoralis, Leucania . J. dA2 Aricia 64, 75, 103, 109, 140, 159, 160
liturata, Selidosoma 5 | mediolucens (obeliscata ab.), Lar-
lividaria, Nychiodes .. 125 entia, Thera 153
livornica, Phryxus .. 59, 140 medionigricans =nigrofaseiata 39
lobengula, Amauris Of .. 95 | Meesia 113
lonicerae, Zygaena .. ..3, 124, 142 | megera, Pararge 4, 23, 24, "29, 124,
lubricipeda=lutea .. 3 Bieet) 139, 142
lucernea, Agrotis 142 | megacephala, Acronicta, Cuspidia 76
lucilla, Neptis : 29 | Megalopyga .. as 82, 83
luctiferellus, Crambus 141 | major (hermione), Nytha, Satyrus 102
luctuosa, Acontia .. 141 | melampus, Erebia .. Aft 2
lunaedactyla iphacodactyla), Mar- meleager, Polyommatus 103, 124
asmarcha .. 5 yah LT mendica, Diacrisia .. So yee chs
lunigera, Agrotis 142 | mensuraria=limitata .. 142
lurideola, Lithosia .. .. 140 | menyanthidis, Pharetra 19
lupulinus, Hepialus ee 82, 83 | melanella=monilifera é Suh yO9.
lutea (lubricepeda), Diacrisia .. 5 | melisanda (ausonia g. a.), Antho-
lutea (flavago), Citria oe -- 140 charis : 30 30 oa Sd)
lutealis, Scopula 56 141 | mercuriana (monticolana), Pam-
lutearia, Cleogene 141 plusia ae od .. 141
luteolata, Opisthograptis 5 | merope (aurinia race), Melitaea 2,
lutescens (napi av.), Pieris 64 30, 139, 143
Lycaenidae . 8, 9, 75, 96, 157 | mersina (semele race), Hipparchia
lycaon, Epinephele .. 120, 123, 139 , 25, 26
lycidas (sephyrus race), Plebeius 2, 30 | meticulosa, Phlogophora .. 5, 141
lychnitis, Cucullia .. : .. 141 | mi, Euclidia.. dc 4,5, 142
Lymantriidae 131 | miata, Cidarint Chloroelysta 21,78, 141
Lypusa ° 82 | midas (alciphron ab.), Heodes 104, 123
lythargyrellus, Grambus 141 | minimus, Cupido 2,5, 105, 122, 140, 165
lyssa (megera race), Pararge 24 | miniosa, Taeniocampa .. -. 129
minorata, Larentia, Perizoma , 14i
mistura (mendica race), Diacrisia 29
SPECIAL INDEX.
PAGE |
mnemosyne, Parnassius BO by
mnestra, Hrebia ..2, 122, 139
moloneyi, Anaphe .. .. 158
moneta, Plusia .. 114
monilifera (melanella), Narycia go) SN)
monoglypha, Hadena 6, 20, ee 142
Xylophasia : :
monogramma, Metoptria 125
monovittata.(sinapis ab.), Leptosia 111
montanata, Xanthorhoé 5, 6, 141
monticolana=mercuriana .. .. 141
morpheus, Caradrina ee 6, 20
morpheus, Heteropterus EDO
Morphinae ae oe .. 146
multistrigaria, Malenydris, Lar-
entia ah ee i 30, 61
munitata, Xanthorhoé -. 141
muralis, Scopula ae PAL
muricata (auroraria), Hois, Hyria,
Ptychopoda 4 SUT
muscaeformis, Aegeria .. .. 142
myrtillata (obfuscaria), Gnophos
~141, 159
myrtilli, Anarta .. 4 6, 20
myopaeformis, Aegeria .. 78
nana (dentina), Mamestra 5, 141, 142
nanata, Hupithecia .. 5 4, 5
napaeae (napi g. a.), Pieris . 64
napi, Pieris 4, 20, 29, 64, 90, 94, 116,
139, 147, 171
neoridas, Erebia ain 22/389
niavius, Amauris .. 14
niceae:(fausta race), Zygaena 105, 124
nictitans, Hydraecia 3 . 20
nigra, Aporophyla 17
nigrescens (sinapis ab.), Leptosia. . . 111
nigricans, Agrotis Be .. 141
nigrofasciata (variata ab.), Larentia,
Thera 39, 40, 41, 88
niobe, Argynnis .. 29,59, 122, 139
noctuella (hybridalis), Nomophila
125, 141
Noctuidae (ina) 76, 132, 140
Notodontidae Us so) he
nouna, Teracolus EAD,
nupta, Catocala 33, 156
Nyctemera .. ave 2. ail
Nymphalidae MELOMS
obelisca, Agrotis ae .. 141
Obeliscata (variata race), Larentia,
Thera 39, 40, 61, 92, 120, 152,
153, 154, 167, 168, 169
obesalis, Hypena .. se 141
obfuscaria=myrtillata 141, 159
obliquaria=rufata . 77
obliterata, Euchoeca ae 8 5
obliterata (variata ab.), Larentia,
Thera oe af oo BY)
obscura (arion ab.), Lycaena 2, 30,
108, 140
obscura (ceto av.), Hrebia .. gD,
**obscura (variata pases Larentia,
Thera ae -. 40
obscurata, Gnophos. . . 141
XI.
PAGE
obsoleta (coridon ab.), ures
matus 66 166
obsoleta (menyanthidis ab. :),
Pharetra 19
obsoleta (thetis), Polyommatus 140, 173
ocellaris, Xanthia, Mellinia 29, 35
ocellata, Mesoleuca. . ..9, 140, 147
ocellatus, Smerinthus 151033
ocellina, Agrotis ; .. 141
**ochrata (cardamines ab.),
Euchloé : 91
ochroleuca, Hadena, Eremobia 30, 141
oeme, Erebia 122
oleracea, Mamestra, Hadena 142
olivalis, ‘Calostigia,. Scopula .. 141
onopordi, Hesperia .. .. 107, 125
ophiogramma, Apamea Ai ngs
opima, Taeniocampa 2
optilete, Polyommatus, Vacciniina 140
**orae (comma race), Urbicola 107, 108
orbicularia, Ephyra. . 717
orbitulus, Plebeius, Latiorina 2, 57, 140
Orgyia 56 GB}
orientalis (niobe race), Argynnis 29
orion, Scolitantides. . ie Pail oe)
Ornithoptera : 148
oxyacanthae, Miselia .. 141
paeninsulitalia (semele race), Hip-
parchia ae Bb S24 a2 Sree G
palaeno, Colias RA ej 29, 139
palaestinensis (titea race), Melan-
argia ot is wy 147
paleacea, Xanthia 5B .. 140
pales, Brenthis 59, 122, 139
palestinensis (belemia race), Antho-
charis i a. 147
pallens, Leucania : .. 142
pallida (carpophaga ab.), Dian-
thoecia .. Se AG
pallida (striata ab.), Coscinia 103, 124
pallidalgirica (semele race), Hippar-
chia ‘ 2 6 Wh
**pallidula (argus ab. ), Plebeius .. 110
palpina, Pterostoma . 125, 140
pamphilus, Coenonympha 5, 20, 29,
30, 139, 142
paphia, Dryas 6, 19, 20, 21, 29, 30,
116, 142, 165
Papilio (onidae) i 75, 132
papilionaria, Geometra .. 6, 140
parthenias, Brephos A). 4, 61
parthenie, Melitaea.. ts 2, BY)
pastinum, Ophiusa, Toxocampa .. 77
pavonia, Saturnia ..4, 130, 140
peltigera, Heliothis. . 59, 141
penella, Heterogynis 82, 83
pendularia, Ephyra, Cosymbia .. 4
penziana, Sciaphila 141
perla, Bryophila .. 140
perlellus, Crambus .. 106, 140
permutana, Peronea a 141
petraria (chlorosata), Lozogramma,
Lithina 5
peucedani (ephialtes race), ‘Zygaena 124
phaeodactyla=lunaedactyla 127, 141
xii.
PAGE |
phaeorrhaea (chrysorrhoea), |
Nygmia O0 20 se 30) |
pharte, Hrebia .. 139
phegea, Syntomis .. 3, 125
pheretes, Plebeius, Albulina 140
phicomone, Colias .. 122, 139
philea =satyrion .. 143
philenor, Papilio 116
philodice, Hurymus, Colias. 149
phlaeas, Rumicia, Heodes 4, 5, 13,
30, 125, 130, 140
phoebe, Melitaea 3 139, 148 |
phocas (dorilis race,) Heodes . 108 |
Pieris (inae) .. 75, 116
pigra, Pygaera 61, 140
pinetata = variata .. -. 154 |
piniaria, Ellopia, Bupalus. . 5
piniperda, Panolis .. ‘ 61
pisi, Mamestra, Hadena no. KG
pitho (pronoé race), Krebia 3, 30
plagiata, Anaitis . 6, 42, 64, 77, 141
plantaginis, Parasemia, Nemeophila
59, 76, 140
platinea, Hadena oP .. 141
Platypterygidae 82
plecta, Noctua 142
plumbaria, Ortholitha 142
**plumbea (euphrosyne ab. h Bren.
this 4 A Sh: Di
plumigera, Ptilophora oI
pluto (alecto race), Erebia . 106
podalirius, Papilio 103, 123, 124,
139, 171
polonus (thetis ab.), Polyommatus 30
polychloros, Eugonia 58, 139, 167
polycommata, Tricopteryx.. 129
polymita, Polia 141
polytes, Papilio fe 147
polyxena, Zerynthia, Thais 29
pomona, Catopsilia .. : 95
popularis, Neuronia ae 141
populata, Lygris, Cidaria .. 141
populeti, Taeniocampa 717
populi, Amorpha 130, 148, 154
populi, Limenitis 1
porcellus, Theretra .. 76, 147
potatoria, Cosmotriche 6, 33
praeaustralis (megera race), Pararge 24
**praeaustralis (alceae race), Hryn-
nis .. 50 Sc O10 .. 106
prasinaria (fasciaria ab.), Hllopia
154, 167
Precis... : Bo a6 -. 145
primulae (festiva), Noctua.. 5
proboscidalis, Hypena 50) al)
procida (galathea race), Melanargia
123, 124
promutata = marginepunctata 141
pronoé, Hrebia fs 3, 30
pronuba, Triphaena.. 20, 29, 30, 140
prosapiaria, Hylaea, Ellopia 61
protea, Hadena +f Seren
pruinata, Pseudoterpna ..6, 125, 142
prunata, Lygyis, Cidaria .. 5, 141
pruni, Strymon 75
SPECIAL INDEX.
PAGE
psittacata =siderata 77
Psodos 50 .. 146
Psychides : .-81, 82, 97
pterodactyla, Stenoptilia .. 141
pudorina=impudens 17
puerpera, Catocala .. 141
pumilata, Hupithecia 26
punctifera (arion ab.), Lycaena 108, 109
punctularia, Tephrosia .. 4, 143
pupillana, Semasia .. 141
purpuralis, Zygaena _ 3, 124, 125, 140
purpuraria, Lythria 30 141
purpurata, Rhyparia 103
purpurata, Arctia .. 125
pusaria, Cabera 5, 6
pusillata, Eupithecia Me bon) we)
pustulata (bajularia), Huchlora 64
putris, Axylia : .. 142
Pyratidae ies 131, 141
pyralina, Calymnia ao. OU
pyrenaica, Hepialus 83
pyrina (aesculi), Zeuzera .. 78
quadrangularis, Amicta ao, Oe
quadrifasciaria, Ochyria, Coremia
78, 142
Quadrifinae .. 17
quadripunctaria (hera), Callimor pha
124, 142
quadripunctata, Caradrina 140
quercifolia, Kutricha 104
quercinaria, Ennomos 78
quercts, Lasiocampa 140
quercts, Ruralis, Bithys 142
ramburi, Aegeria .. 140
ramosa (aurita ab.), Setina 125, 140
rapae, Pieris 4, 16, 20, 90, 146, 139
rectilinea, Hyppa .. ae s5. JUsiy)
reducta (obeliscata ab.), Larentia,
Thera ; .. 153
repandata, Boarmia 14
resinella, Rhyacionia 4 141
reticulata (saponariae), Neuria 76
revayana, Sarrothripus 92
rhadamanthus, Zygaena .. 125
rhamnata=transversata U1; 93
rhamni, Gonepteryx . 4, 21, 139
rhododactylus, Cnaemidophora 141
rhomboidaria (gemmaria), Boarmia
80, 125
rhomboidea=stigmatica a6 0G
Rhopalocera . . a4 si6 ES
richardsoni (vinculella), Tinea 84, 113
ridens, Asphalia a 61, 92
ripartii (admetus race) Polyom-
matus, Hirsutina 103, 104, 123, 124
rivata, Xanthorhoé, Larentia 5, 78, 89
rivularis (camilla), Limenitis 2,
59, 105, 127, 139
roboraria, Boarmia .. i .. 165
rippertaria, Lithina 141
roboris, Laeosopis .. -. 103
romanovi (discobolus ab. ) Par-
nassius .. 147
rosea (glariosa ab.), Noctua 76
SPECIAL
PAGE
rostralis, Hypena .. -. 130
rubi, Callophrys 5, 142
rubi, Lasiocampa .. 140
rubidata, Anticlea .. 78
rubiginata, Leptomeris, Acidalia, . 125
rubiginea, Dasycampa po 0
rufata (obliquaria), Chesias 77, 92
rufina =helvola 50 56 .. 140
rufimitrella, Adela . i 141
rumicis, Pharetra, Acronicta 142
rurea, Xylophasia .. O16 5, 6
russula = sannio 124, 125
gacraria, Sterrha 64
sagittata, Larentia .. 89
salicis, Leucoma f ss ..- 149
salmacis (medon ab.), Plebeius,
Aricia uy .. 64
sambucaria, Ourapteryx 129
sannio (russula), Diacrisia 6, 124, 125
sao, Pyrgus, Hesperia .2, 105, 140
saponariae = reticulata -. 76
satyrata, Hupithecia 93, 147
Satyridae bee 56 .. 146
satyrion (philea) (arcania race),
Coenonympha , 139, 143
saucia = margaritosa 76, 141
scabiosata, Hupithecia 93
schepdaeli (cardamines ab.), Eu-
chloé ad 29, 91
schmidtii (phlaeas ab. ), Rumicia.. 30
scipio, Hrebia ae -. 124, 139
scolopacina, Xylophasia .. 76
scota (semele race), Hipparchia 21,
, 23, 26
scotica (variata race), Thera,
Larentia .. 39, 40
secalis (oculea) (didyma), “Apamea
20, 129
segetum, Agrotis .. 142
selasellus, Crambus. . ae .. 141
selene, Brenthis ..30, 96, 142
semele, Bippereps 21, 22, 23, 24,
26, 64, 126, 139, 142
semiargus, pogo (Cyaniris) 140
senthes (semele race), Hipparchia
24, 26
sephyrus, Plebeius .. 2, 30
sepiaria, Tephrosia .. -. 141
serotinaria, Gnophos 509, 141
sertata, Lobophora, Acasis.. 89
sexstrigata (umbrosa), Noctua 76
sibilla, Limenitis 2 .2,,6,.;,30
siciliana (semele race), Hipparchia
21, 24,25, 26
sidae, Hesperia 29
siderata (psitticata), Cidaria 77
silaceata, Eustroma, Larentia 5, 89
similis =chrysorrhoea .. 20
simplana, Hedya 13
simplonia, Agrotis .. 141
simulans, Agrotis .. 141
sinapis, Leptosia 59, 110, 111, 125,
139, 142
sobrinata, Eupithecia is 93, 141
sociata, Larentia, Xanthorhoé .. 5
INDEX.
sociella, Aphomia
sophialis, Botys BY
sordida (anceps), Mamestra
sordidata =fureata ..
spadicea=ligula .. ae fe
spini, Strymon 103, 104, 125,
spheciformis, Aegeria
Sphingidae
statices, Adscita
statilinus, Satyrus ..
stellatarum, Sesia, Macroglossa 130,
140,
stigmatica (rhomboidea), Noctua ..
stoechadis, Zygaena ds ae
stragulata (variata ab.), Larentia,
Thera 89, 119, 120, 151, 152,
straminea, Conchylis, Kuxanthis ..
straminea, Leucania
striata (thetis ab.),
striata, Coscinia
76,
78,
76,
Polyommatus
103,
strigata (thymiaria), Hemithea 6,
strigata (vibicaria ab.), Rhodo-
strophia
strigillaria, Perconia, Aspilates
strigilis, Miana :
stygne, Erebia 105, 106, 122, 124,
subalpina (dorilis race), Heodes
subaudiata, Triphosa ;
subcalida (medon race), Plebeius,
Aricia é 109,
subnotata, Kupithecia 78,
substitutus (apollo race), Parnassius
succenturiata, Kupithecia ..
suffumata, Lampropteryx .. 5, 92,
suffusa = upsilon BY fe
suffusa (semele race), Hipparchia
suspecta = iners 5 Pe o6
sylvanus, Augiades .. 6,
sylvina, Hepialus 5:5
sylvina, Mesosemia. .
syringaria, Hygrochroa, Pericallia
tages, Nisoniades 4, 5, 6,
taraxaci, Caradrina.. tee
taraxaci, Lemonia .. iG :
dicignoniiraa eee 3h
telicanus, Syntarucus aig By 1),
fenebrata, Heliaca .. as
teres (Semele race), Hipparchia 23,
24, 25,
terrea, Caradrina .. 00
tersa (armoricanus race), Hesperia
tersata, Phibalapteryx, Horisme7s8,
tersior (onopordi race), Hesperia ..
testacea, Apumea, Luperina
thapsiella, Depressaria Ee
thaumas = flava 56 He 6,
theophrastus, Tarucus ab 8,
thetis, Polyommatus, Agriades 6, 7,
30, 59, 67, 116, 127, 140, 165,
thore, Brenthig ie 29,
thymiaria =strigata
Thysania ac
tigris, Amphicallia ..
tiliae, Mimas
Tinea sie sie
19, 42, 76,
xiv. SPECIAL INDEX; |
PAGE
tineana, Ancylus .. As of NLS
tipuliformis, Aegeria 78
titan, Ornithoptera .. 148
titea, Melanargia .. GI -. 147
tithonus, Epinephele .. (142, 165
tityus (bombyliformis), Hemaris .. 5
togata, Kupithecia .. : 78
tolana (cristana ab.), Peronea 96
Tortrices . 141
tosna, Suastus é =o}
trabealis, Agrophila.. 125
tragopogonis, Ampbipyra Ke 140
transalpina, Zygaena 3, 80, 105,
123, 124, 125, 140
transiens (sinapis race), Leptosia. . 111
transversata (rhamnata), Philereme
Cos: Oe
trapezina, Calymnia 2. 28
trepida, Notodonta .. ey 125
triangula (ausonia race), Antho-.
charis 3 std nF 90
Trifinae Bo Set)
trifolii (chenopodii), Hadena 141, 147
trifolii, Lasiocampa soos Of OO
trifolii, “ygaena.. oe , 140
trimacula, Derthisa, Hpisema 141
tripartita, Abrostola 141
triplasia, Abrostola .. 148
tritici, Agrotis 141
Troides ee .. 132
turcica (galathea race), Melanargia 124
turfosalis, Schrankia Cache
tyndarus, Hrebia .. ae 60, 139
typhae=arundinis .. ais oe 07
ubaldus, Azanus .. Saraa9
ulmifolia (quercifolia race), Eu-
tricha, Lasiocampa 104
umbra (marginata), Chariclea 77
umbratica, Cucullia 147
umbrosa = sexstrigata f 76
unangulata, Xanthorhoé, Eupbyia 142
uncula, Eustrotia, Hydrelia 77
unicolor (lutea ab.), Diacrisia
unicolor Gorampeling ab.), Cir- |
rhoedia ie DAO
unifasciana, Tortrix 148
unifasciata = bifasciata 158
upsilon (suffusa), Agrotis .. 141
urticae, Aglais 6, 20, 21, 58, 139,
143, 144, 156, 166, 167
urticata, Eurrhypara 171
valesina (paphia ab.), Dryas 19, 20, 29
v-argenteum, Plusia 141
varia, Melitaea th cag? 29, 139
variata, Larentia, Thera 39, 40,
61, $8, 89,.90, 92, 119, 120, 151,
152, 153, 154, 167, 168, 169
variegana, Peronea.. us oe. esi
vauaria, Halia 141
venata, Anaphe 158
venosata, Hupithecia 43 -. 141
verbasci, Cucullia ... ..4, 130, 142
verberata, Coenotephria .. 141
verhuellella, Perr ole, Psychoides
2 65, 68, 82, 83
PAGE
versicolora, Dimorpha, Endromis.. 76
**veris (argus race), Plebeius a0 110
vernaria, Geometra.. 11 na 147,
vespiformis (asiliformis), Aegeria.. 78
vibicaria, Rhodostrophia’ 102, 125, 141
villica, Arctia Os af 42, 130:
vinculella (richardsoni), Tinea 82,
84, $3, 113.
viningra, Aslauga ... a -- 160:
vinula,. Cerura ob vf. .. 140
virens, Leucania .. re .. 140
virescens, Charagris 80
virgaureae, Heodes 2, 103, 122, 124, 140
viridaria, Phytometra ce 5
viridaria, Amoebe, Larentia 5, 6
viridella, Adela Ny E 82, 83
vitalbata, Philabalapteryx, Horisme 78
vitellina, Leucania .. 140
vitiosata (variata ab.), Baventin
Thera axe ve .. 119, 120
vittata =lignata a Be Rarities:
vulgata, Hupithecia. . ie 5, 93
wahlbomiana, Sciaphila .. .. 141
w-album, Strymon .. bi 75, 104
xerampelina, Cirrhoedia .. faut20
Zeuzeridae ... oft iy sHinS 2
ziezac, Notodonta .. 76, 130, 140
Zygaena (idae) 48, 82, 85, 124, 129, 132
NEUROPTERA.
bioculata, Ephemera he «+ LOS
italicus, Ascalaphus ie -. 60
longicornis, Ascalaphus .. .. 125
Myrmeleon .. ae en li2,
pellucida, Hydropsyche ae dal fe
perla, Chrysopa .. ae .. 125
Phryganeidae af 56 a0)
prasinus, Chrysopa .. oo .. 125
ORTHOPTERA,
Avixenia 5 ow Cine 0
berenguieri, Barbitistes bis .. 103
crucigera, Ephippigera: ae .. 124
egena, Hmpusa As SG .. 104
Empusa a oc S10 .. 147
EKphippigera - . 56 at Bo ates
Forficulidae .. O10 OG .. 82
nivea, Panchlora .. os SOG
religiosa, Mantis .. ci oe als
scalaris, Stauroderus at .. 103
serricauda, Barbitistes Aes .. 104
virescens, Panchlora a0 Ee UZ9
PARANEUROPTERA.
Aeschna ce SY .. 104
annulatus, Cordulegaster We LO 4 25
caerulescens, Orthetrum 1038, 104, 125
cyanea, Aeschna .. ae .. 60
dubia, Leucorrhinia. mM Seeing 2:
flaveolum, Sympetrum .. eH:
forcipatus, Onychogomphus 104, 125
grandis, Aeschna .. .-- 148
haemorrhoidalis, Calopteryx 104, 125
SPECIAL INDEX. XV.
PAGE PAGE
juncea, Aeschna .. a .. 172 | melanoderes, Dysdercus .. .. 158
Lestes ie : Ne .. 60 | m-flavum, Monodesmus .. oo IPAS
mercuriale, Agrion . .. 105, 172 | najas, Gerris Se $0 Diy cndlis)
nymphula, Pyrrhosoma ie .. 125 | nebulosa, Aphalara.. Me yous Od
scoticum, Sympetrum SO .. 60 | nigricans, Carpocoris Ae .. 126
splendens, Calopteryx .. 104, 125 | pallida, Flata : a: .. 158
striolatum, Sympetrum .. .. 60) pandurus, Spilotethus oo .. 126
perplexus, Pilophorus se .. 136
RHYNCHOTA. personatus, Reduvius .. 105, 126
| Phonoctonus.. ; 50 .. 158
acuteangulatus, Gonocerus -- 126 | picturatus, Phonoctonus .. <3158
agilis, Stenocephalus ais .. 124 Pilophorus ar ie -. 136
Aphididae .. a -- 145 | queretis, Stomaphis. . 73, 137, 138
baccarum, Dolycoris | a -- 126 | syadicis, Trama ee ee 5
carnosa, Geoica aie 96 so UB remigis, Gerris ni i Me 5
clavatus, Pilophorus 8 -- 136 | sanguinolenta, Cercopis .. 59 1G
Coccidae 28 -- 48, 176 | caxatilis, Spilotethus as .. 126
donisthorpei, Ripersia oc so LAG Stomaphis .. ey ig _. 136
dumosa, Jalla 0 oh -- 126 | cubterranea, Ripersia ag eds
Dysdercus — .. = -- 158 | superstitiosus, Dysdercus .. soy US
equestris, Spilotethus BO -- 126 | theivora, Helopeltis a aiey ee
floccosa, Newsteadia ie so: 08) || eihaah. JakReayrinn 146
formicaria, Forda .. ie 55) 083 ; ah Fs i
formicina, Gesica .. ie 60 | Ue)
formosus, Phonoctonus .. so WE | NOT CLASSIFIED.
fosteri, Psylla ae als .. 88 | albinos, Cyphodeirus (Collem.) 74,
fraxina, Cicada ae A .. 126 138, 176
Fulgoridae .. : sie .. 96 | Amphisbaena (Rep.) ati eo)
iracundus, Harpactus 60 .. 126 | annulosa, Caecilia (Rep.) .. es Ue)
Lachninae .. ac .. 137 | aquatica, Podura (Collem.) sa WZ
lateralis, Campotopus oie .. 126 | **corticis, Coecilius (Psocid.) .. 148
Laternaria .. Be so Ulals Hiaeiidae! Bie aie 32, 46
lineata, Graphosoma 0 .. 126 fragilis, Anguis (Rep.) oe 74, 75
ikon ir Piezodorus ae .. 124 | gigas, Scolopendra .. u 95
longirostris, Stomaphis .. 136, 137 | hoffmanseggii, Platyarthrus (Crus. )
longirostris (=quercus), Rhyn- 74, 138
chocles .. ae fe .. 137 | Platyarthrus (Crus.) ee so
Macroceraea . . Sia a bo Lye
ae
hh
ep
. , f
okie 3
or
ae
Fie
yh
nb
SEASONAL POLYMORPHISM. (21)
from chariclea, Steph., in the lowlands, chiefly by consisting of indi-
vidual forms transitional to vazquezi, Obth., Ht. Lép. Comp., IX., IL.
part, p. 89, fig. 2207 (May, 1914) [‘‘ Castile, in Spain ’’], and by pro-
ducing well characterised ones of the latter quite frequently. I will
deal more at length with all these points in the paper mentioned there.
I only wish to remark here that Réber’s catoleuca is not an Oriental
race, but that it is the second generation of the whole of southern
Europe. In Italy it stops short on the boundary of the Peninsular
subzone, and it is replaced in the Po Basin by nymotypical brassicae,
which extends northwards to the whole of Central and Northern
Hurope. My August specimens from Norrwegen, in Central Sweden, and
from St. Petersburg, are identical with those from Vienna and Northern
Italy. I conclude that, as Stephens by creating his name of chariclea,
restricted the specific one to the summer form, there is no use for
Rober’s lepidii, which he has simply given to the summer form in a
general way, because he considered the spring form to be the nymo-
typical one. One does meet commonly in Central Kurope, both indi-
vidually and locally, with a form which points to aestiva =catoleuca of
the south by its large size and very scanty dark sealing on the underside;
this is presumably not found in Sweden, but I see no way and no
reason to use the name of lepidii for it in particular, nor to give it any
other designation but that of trans. ad aestiva. As to the third genera-
tion of southern Kurope I have called tertia, I am not fully satisfied that
it is not perfectly identical with the second of northern Europe (which
is also the most usual in Central Europe), and consequently nothing
but nymotypical brassicae, L. In this species, too, Zeller’s names have
the right of priority and must be used: that of verna is the oldest given
to a southern form, and in consequence the entire race, as well as the
first generation, must be designated by it; the other is aestiva, given
to the second generation of Syracuse, collected ‘‘ from the end of May
to June 22nd”; this is nothing but catoleuca, Rober, identical with my
Syrian examples, as it is with Tuscan, Spanish, and others from the south
of Hurope, so that catoleuca falls before aestiva, which applies to the
very distinct second generation of the entire Mediterranean region.
Also the name of mertdionalis, proposed by Roeci for the southern
summer generation, with which he mixed up the second and the third as
one, falls before aestiva, Z. (R. Verity.)
Tribe : Aportidi.
Aporia crataeyi, Li. [‘* Sweden.’ }
(a) race meridionalis, Vrty., Rhop. Pal., p. 824, pl. LXVLI., f. 8.
January, 1911 [‘Syria’’].—C.It., up to 1800m.
(b) race crataegi, L., trans. ad minor, Vrty., Rhop. Pal., p. 119, pl.
XXVI., f£. 8-9 (October, 1907) [Vernet-les-Bains, Pyrénées
Or.” |.—C.It., from 500 (Mainarde Mts.) to 1300m. (Pian
di Gra in the Sibillini Mts. in the Marche).
(c) race augusta, Trti., trans. ad crataegi, L., (Vrty., H.R., 1921, p.
192)—Calabrian Coast Range, 900m.
Family : Papilionidae.
Tribe: Parnasstidi.
Parnassius mnemosyne, L. [** Habitat in Finlandia.’
(a) race costantinii, Trti., Soc. Ital. Scienze Nat., 1919, p. 162, and
(22) THE. ENTOMOLOGIST’S RECORD.
1923, pl. B, fig. 1-6.—“ Mt. Cimone, 1600m., on boundary
between Modenese and Tuscan Apennines.”
(b) race fruhstorferi, Trti., Nat. Sic., 1909, p. 34, t. I., f. 1-2 (Mb.
Autore in the Abruzzi.”)—C.It., 1200-1600m.
(c) race aquilensis, Bryk. (Trti., U.c., 1919, p. 163).—‘* Gran Sasso
d'Italia, in the Abruzzi.”
(d) race calabrica, Trti., Ann. Museo Zool. Napoli, 1911, p. 12, and
Soc. It. Sc. Nat., 1915, t. VIL, f. 18-17, (‘‘ Aspromonte in
Calabria.””)—Calabria, 900-1700m.
Parnassius apollo, L. [‘* Frequent in Sweden.’ |
(a) race apenninus, Stich., Gen. Insect., 1907, p. 26, (“ Type”:
Verity’s figure in Rhop. Pal., pl. VIII., fig. 20).—* Altissimo
Mt., 1000m. in the Apuane Alps.”
(6) race emilianus, Trti., Atti. Soc. Ital. Scienze Nat., 1923, p. 31 of
extract, pl. A.—‘‘ Mt. Cimone, 1600m., on boundary between
Modenese and Pistoiese Apennines (Northern Tuscany).”
(c) race euappenninus, Vrty., B. Soc. Hint. It., XLY., p. 206 (1914).
— Sibillini Mts., 1800 to 2000m.”’
(d) race decoratissima, Vrty., E.R., 1919, p. 88.—* Pratofiorito
Mt., 1200m. above the Baths of Lucca, and Gran Sasso
d'Italia in the Abruzzi.”
(e) race ttalicus, Obthr., Et. Lép. Comp., II1., p. 116.-—“* Majella
Mt., 1500m., in the Abruzzi.”
(f) race pumilus, Stich., Berl. Ent. Zeit., 1906, p. 88 (locality of
‘types’? unknown).-—Aspromonte, 1200 to 1800m., in
Calabria.
Tribe: Zerynthiidi.
Zerynthia hypermnestra, Scop. [‘‘ Carniolia.’’]
(a) race cassandra, Hb., H.S., £. 910-913 (1823-1838) [no text to
typieal figure}. (= latiaris, Stichel in Wytsman’s Gen. Ins.,
p- 11 (1910), “ Mt. Cavo, 800m., near Rome.’’)—C.It., up to
1000m., in river beds. Stauder has found the species on the
Aspromonte in Calabria, but we do not know whether it
belongs to this race or to latevittata, Vrty., as in Sicily.
Note.—Stichel (l.c.) calls cassandra, Hb., a ‘“ nomen irritum,” and
replaces it by that of creusa, Meig., Syst. Bearb. Hur. Schmett., I., p.
161 (1829). I suppose he does this because there is no text to Hib-
ner’s figure. On this ground, however, most names of this author
would have to be discarded, and I do not think entomologists are quite
prepared to adopt this useless revolution in Nomenclature. Hiubner’s
figures represent most perfectly the race of Central Italy, as I have
pointed out in #.R., 1919, p. 88, where I also described and named
latevittata, the much darker form, usually called cassandra, quite
wrongly. Specimens from Florence and Marina di Pisa in my collec-
tion, Mt. Autore and Albani Mts., in Turati’s, are all quite identical. The
name of latiaris is thus nothing but a synonym. In Liguria there
exists a peculiar race described by Fruhstorfer under the name of
reverdini, in the Intern. Entom. Zeit. Guben., 1908, p. 58, from speci-
mens collected at ‘‘ Rapallo’’ by Reverdin; he says that it is considerably
larger than race creusa, Meigen, of Southern France, and also than
latiaris, and that the yellow ground-colour is unusually light in tone
and extensive, the black pattern being very reduced in extent.
RRA E MNT 77k PL a dela UL CCT
SEASONAL POLYMORPHISM. (23)
Reverdin has kindly sent me his three specimens and left me one for
my collection. They are similar to the cassandra individuals from
Florence of the largest size and with black pattern most reduced in
extent; the black band of hindwings strikes me especially as being
narrower and not as dark as in most cassandra from Central Italy.
(R. Verity.)
(6) race nemorensis, Vrty., H.R., 1919, p. 88.—C.It., in woods
(“ Forte dei Marmi, in the Proy. of Lucca, on coast ’’).
Tribe: Papilionidi.
Papilio machaon, Li. {‘* Sweden.”
(a) race emisphyrus, Vrty., H.R., May, 1919, p. 88 (‘Florence ’’).—
I. gen. emisphyrus, Vrty.; IL. gen. sphyroides, Vrty., Rhop.
Pal., p. 12, pl. IL., f. 6 (reprint of part 1 in 1908), (‘ Forte
dei Marmi, on Tuscan coast’’); LIL. gen. sphyroides, Vrty.—
C.It., up to 1300m.
(b) race meridionalis, Rocci., Soc. Lig. Sc. Nat., April, 1919, p. 11,
pl. L., f. 3 (“ Genoa in Liguria ’’); II. gen. sphyroides, Vrty. ;
JIL. gen. sphyroides, Vrty.—Southern It.
Note.—Although we have not seen extensive series from Southern
Italy, we think we can agree with Stauder (Mitt. Miinchener Ent. Ges.,
1922, p. 17) that the first generation is different from the one of
Central Italy. In Northern Italy, at low altitudes, form emisphyrus
exists alone; in the Alps, at high altitudes, it is replaced by race alpica,
Vrty. In Tuscany (and in Liguria according to Rocci) the darker
form, meridionalis, is always met with mixed with the lighter form,
emisphyrus, whereas in the province of Caserta and the Neapolitan
district, we have only found the former. A series of grades is thus
detectable leading from race bigenerata, Vrty., H.R., 1919, p. 88, with
its second generation aestivoides, Vrty., of Central Europe, to the fol-
lowing race characteristic of Sicily, and beyond it to the extreme
melanic urticensis, Rocci, peculiar to the small islands of Ustica.
(c) race sphyrus, Hb., E.S., f. 775-776 (1828) [no text to typical
figure.| —I. gen. sphyrus, Hb.; Il. (and III. ?) gen. aestivus,
Zeller, Isis, 1847, p. 216 [** Syracuse, in Sicily”’]; IV. (or
IIL. ?) gen. revertens, mibi.— On the Aspromonte Mass in
Southern Calabria, up to 950m.; according to Stauder, Zert.
wiss. Insektenbiol., 1915, p. 289.
Note.—At Delianova, 600m., this author met at the end of Septem-
ber and in October, with specimens very strongly resembling the first
generation. He supposes them to be the third generation, but both
by the date and by their features it seems more likely they should
constitute a fourth partial generation. It has been suggested that
Hiibner’s figure of sphyrus represents an aberration, with much more
blue scaling on band of hindwings than is ever normally found in
nature. This is quite a mistake, as several specimens of the first
generation from Palermo, in Sicily, and two from England in my
possession, agree perfectly in every detail with that figure. It is quite
remarkable that I should not have been able to detect any difference
between the first gencration from Sicily, called vernus by Zeller (/.c.),
and the English race, called britannicus by Spengel, so that both these
names would seem to fall before sphyrus, Hub. (R. Verity.)
Papilio alexanor, Esp. [‘* Nice, in Provence.’ |
’
(24) THE ENTOMOLOGIST’ S RECORD.
(a) race alecanor, Esp.—Aspromonte, 1200m., in Calabria, accord-
ing to Turati. Verity has made sure of the race by seeing
the specimen.
Iphiclides podalirius, LL. (Type: description of Raio, Hist. Ins., p. 111,
n. 3: ‘near the port of Leghorn in Tuscany.” Habitat in
‘southern Kurope and Africa,’”’ according to Linneus).
(a) race podalirius, L.—l. gen. podalirius, L.; Il. gen. zanclaeus, Z.,
Ists, 1847, p. 218 [‘‘ Messina, in Sicily’’]; IIL. gen. zanclaeus,
Z.—P.It., up to 13800m.
(6) race interjecta, Vrty., Rhop. Pal., p. 291., pl. L, f. 8 (January,
1911) {‘ Akbes, in Syria’’].—I. gen. interjecta, Vrty.; II.
gen. zanclaeus, Z.; Il]. gen. zanclaeus, Z.—Calabrian coast
range, 800m.
Division : Nymphalida.
Family ; Satyridae.
Subfamily : Hpinephilinae.
Tribe : Coenonymphidt.
Coenonympha tiphon, Rott. [‘ Landsberg on the Warte, in Germany’’}.
(a) race italica, Vrty., Soc. Ent. It., 1918, p. 222, pl. 1, f. 24-27.—
C.It., at very high altitudes (‘‘ Sibillini Mts., 1600m.”).
Coenonympha pamphilus, L. [ Sweden.” ]
(a) race emiaustralis, Vrty.—I. gen. emiaustralis, Vrty., with the
precocious group murina, Vrty., H.R., 1919, p. 121; II. gen.
aestivalis, Rocci, Soc. Lig. Sc. Nat., 19138, p. 5 (“ Northern
and Central Italy (Turin) ’’).—C.It., from 1000 to 1300m.
(6) race australis, Vrty.—I. gen. australis, Vrty., Soc. Ent. It., 1914,
p. 22, f. 88-39; II. gen. aestivalis, Rocci.—P.It., in damp
surroundings up to 1000.
(c) race emilyllus, Vrty.—I. gen. australis, Vrty.; II. gen.: early
emergence enilyllus, Vrty., H.R., 1919, p. 122, “ Florence,”
and late emergence aestivalis, Rocci.—P.It., in dry surround-
ings up to 1000m.
(d) race latenigrata, Vrty.—l. gen. australis, Vrty.; U1. gen. latent-
grata, Vrty., H.R., 1919, p. 122.—C.It., in hot and damp
surroundings on coast (‘‘ Casciana near Pisa,” Pertusola near
Spezia, Lago di Porta in the Prov. of Lucca).
(e) race lyllus, Lsp.—I. gen. sicula, Zeller, Isis, 1847, p. 146
[(‘“‘ Messina and Syracuse, in Sicily] ; II. gen. lyllus, Esp.,
Schmett., I., 2, pl. 122, f. 1 (1806) [** Portugal ”’] .—Stauder
records lyllus, Hsp., from the Aspromonte in Calabria (Polsi
and Gioia Tauro), and, although it will be well to have a
confirmation that it really is race lyllus, as in Sicily, it seems
highly probable it should be so, considering the races from
the far end of Calabria often are similar to the Sicilian ones.
Descriptions of the races and forms of pamphilus quoted above
have been given by Verity in this journal for 1916, p. 171,
and for 1919, p. 121.
Coenonympha arcania, L. [‘* Sweden.”’]
(a) race tenuelimbo, Vrty.—I. gen. tenuelimbo, Vrty., Soc. Hut. It.,
1914, p. 223, t. I. f. 28-80; II. gen. gracilis, Vrty., E.R.,
1919, p. 123, < Florence.!’—C.It., from sea coast (Querci-
anella, near Leghorn) up to 1300m.
" SEASONAL POLYMORPHISM. (25)
Note.—In my original description of this race I stated that it was
widespread in Southern Europe, and I mentioned the Valais and
Barcelona as localities whence I had specimens, besides the ‘‘ types”’ I
figured from the Sibillini Mts. and Florence, in Central Italy. Subse-
quently I have found that, in fact, the race of Peninsular Italy is not,
on the whole, the most extreme by the narrowness of the marginal
band above; males in which it is as narrow as the one I have figured
are quite scarce; Swiss specimens exhibit it more frequently in this
sex. I must mention that on the 15th of July, 1913, I collected two
lageard females of the first generation at La Traversa, 1100m., on the
Futa Pass road (prov. of Florence), both of which exhibited the
characteristic of form Auwebneri, Obth., in having the hindwings broadly
fulvous at base above. It will be interesting to find out whether this
character, which we have never seen in other localities, is constant or
prevalent in that one, or in others similar to it, and whether it is thus
racial. Oberthiir, who gave the name in Et. Lép. Comp., LV., p. 25
(1910) to Hubner’s figure 240 (with no text), had only one male from
Roccaraso or Paleno, in the Abruzzi, and one from Mentone in Southern
France. My fig. 30, of tenuwelimbo represents one of my two females
of huebnert. (R. Verity.)
(b) race opposita, Vrty., Soc. Hnt. Ital., 1914, p. 224, pl. L, p. 31-
338=tyrrhena, Stauder, Zeit. wissensch. Insektenbiol., 1915, p.
1, pl. IL., p. 17; UL. gen. unknown.—Calabria, up to 1200m.
(‘« Piani de Carmelia, 1200m., on Aspromonte’’). Stauder’s
tyrrhena is described from Mt. Martinello, 1000m., in Cala-
bria, but he also includes specimens from the Sorrento
peninsula (Mt. Faito, 1100 to 1200m., and Mt. Pendolo
500m.). As he only had one Calabrian specimen, which he
considers his ‘‘ type,” it may be found out that the Sorrento
race 1s not, on the whole, as he thought, the same as the
Calabrian one; especially the Mt. Pendolo one, described as
smaller, may be a race tenuelimbo trans. ad opposita, Vrty.;
the name of tyrrhena may turn out usefal for the Mt. Faito
race, if it is only a further grade of transition.
Coenonympha corinna, Hb. [‘ No text to figure.’’|
(a) race elbana, Stgr.—l. gen. elbana, Ster., Vat.,1901, p. 66; II.
gen. altera, Vrty., Soc. Hint. It., 1917, p. 191.—Isle of Elba
up to 500m.
Note.—I must take this occasion to point out that Bonelli’s norax is
in no way simply a synonym of corinna, as it is considered by all authors.
Bonelli himself very rightly states, in his Appendix of 1825 to the
paper of March, 1824, that his insect is different from Hwbner’s figure,
and his own excellent figures clearly represent the very distinct second
generation of Sardinia, corresponding perfectly to altera, Vrty., of race
elbana, Stdgr.; IL. gen. norax, Bon., must, accordingly, come into use.
(R. Verity.)
Coenonympha dorus, Esp. [‘* Languedoc in Southern France.”
(a) race dorus, Ksp.—C.It., very locally, up to 1200m. (Assisi in
Umbria, according to Wheeler; Bolognola on the Sibillini
Mts., in Vrty. coll., found by Querci; Abruzzi, according to
Calberla) ; it has never been found in Tuscany.
Coenonympha iphis, Schiff. [* Vienna.’’ |
(a) race iphis, Schiff—Mt. Antore, 1400m., in the Abruzzi. Verity
(26) THE ENTOMOLOGIST’S RECORD.
possesses specimens collected by Rostagno in this locality.
Calberla records it from ‘the Gran Sasso, on swampy
mountain meadows, in July.”
Tribe: E'pinephilidi.
Pyronia ida, Wisp. {** Pyrenees.’’ |
(a) race ida, Esp.—Isle of Elba up to 500m.
(6) race neapolitana, Obthr., Et. Lép. Comp., III. (1909), p. 392
and V. (1911), f. 677 and 682 (“ Pompei, near Naples,’’) =
arminti, Stauder, Zeit. wiss. Insekt., 1916, p. 62 (‘*Bed of
Buonamico, on Aspromonte, at various altitudes ”’).—P.1t., up
to 900m.
Pyronia tithonus, L. [* Germany.”’|
(a) race tithonus, L.—C.It., hot and damp localities on coast (Isle
of Elba up to 600m.; Forte dei Marmi, in the Prov. of
Lucca.)
(b) race transiens, Vrty., H'.R., 1919, p. 123.—C.It., in damp sur-
roundings, up to 700m.. (“Pian di Mugnone, in deep
gullies, near Florence.’’)
(c) race etrusca, Vrty., E.R., 1919, p. 123.—C.It., in cold and dry
surroundings, up to 1200m. (“ Mt. Conca, 400m., near
Florence.”’)
Hyponephele lycaon, Rott. |‘ Landsberg-on-the- Warthe, in Germany.’’]
(a) race analampra, Trti., Nat. Sic., 1909, p. 70, t. II., f. 18-19.
(Mt. Majella and Gran Sasso, in the Abruzzi.’’)—C.It., on
high mountains, 1200-1400m.
(brace anacansta,. Uri, sat, sic. 1909) sp. Wil tee tal to.
[‘‘Madonie Mts., in Sicily, and Algeria.”]|—-Mt. Cairo,
1500m., in the Prov. of Caserta.
Hyponephele Lupinus, Costa; (‘‘ Bosco di Guagnano, 44m., in the Forest
of Terra d’Otranto in the Proy. of Lecce.”’)
(a) race intermedia, Stgr., Stett. ent. Zeit., 1886, p. 251 |‘ Cau-
casus ’’?].—Northern part of C.It. (Mt. Fanna, 600m., near
Florence).
(6) race lipinus, Costa.—Forests of Terra d’Otranto (Lecce).
EHpinephele jurtina, L. [‘* Sweden.’’|
(a) race phormia, Fruhst., Int. Hut. Zeit. Guben., 14 Aug., 1909,
p- 117 [‘‘Meran in 8. Tyrol’’}.—C.It., at high altitudes,
1000-1300m.
(b) race prachispulla, Vrty., E.R., 1921, p. 210 (‘‘ Florence ”).—
C.It., up to 900m., and presumably Southern Italy.
(c) race emihispulla,* Vrty., E.R., 1919, p. 128.—* Poggio, in the
Isle of Elba, 450m.”
Subfamily: Hrebiinae.
Tribe: Oeneidt.
Genus: Hrebia.
Note.—We have adopted the classification of this genus worked out
by the late Dr. Chapman (Tr. Ent. Soc. London, 1898, pp. 207-288, pl.
V.-XVI.) according to the male appendages, although a grouping of
species based on a single set of characters does not satisfy one that it
really expresses natural relationship as fully as possible, and its author
was the first to make this remark.
SEASONAL POLYMORPHISM. (27)
Group I.
Subgroup: a.
Hrebia ligea, Li. [‘* Sweden.’’|
(A) Subspecies ligea, L.
(a) race siscta, Fruhst., Soc. Hnt., 1909, p. 125.—C.It., from 800 to
1300m. (Tuscan Apennines, Sibillini Mts., and ‘“ Gran
Sasso,” in the Abruzzi.)
(B) Subspecies philomela, Hub. [‘ Prealps of Tyrol and Riesenge-
birge’’] =euryale, Esp. [* Riesengebirge, in Silesia.’’]
(a) race apenninicola, Vrty., Bull. Soc. Ent. France, Oct., 1911, p.
312, pl. I., f. 8-4.—Tusean Apennines, from 1800 to 1800m.
(‘Il Teso, in the Pistoiese.’’)
(6) race brutiorum, Trti., Ann. Mus. Zool. Univ. Napoli., Sept. 1911,
n. 18.—‘‘ Gran Sasso, in the Abruzzi,” according to Turati.
Note.—I deal with ligea and philomela as belonging to a single
species, because it seems to me their complicated and. perplexing
relationship is one of the cases which should be kept clearly apart from
the higher gerade of distinctness one calls ‘“ specific,” consisting in two
groups whose individuals are, without exception, perfectly distinct from
each other. The Hrebiae in question seem instead to be due to a phe-
nomenon similar to that of Nytha fagi, with its two fagi (=alcyone)
and major (=hermione), groups of races, and perhaps, to a certain
extent, also similar to Melitaea athalia, with the athalia and pseudo-
athalia groups. It seems as if one should conceive these two groups
as consisting in two diverging series of races, which spring from an
intermediate one and gradually get more and more distinct from each
other, till the extreme races afford a degree equal to the specific one,
so that they can inhabit the same grounds without intermixing. This,
I think, is the true sclution of the vevata questio about adyte, Hub.,
which some ascribe to ligea and others to philomela, whereas it is per-
fectly intermediate. The phenomenon mentioned above I propose
calling of ‘twin subspecies.” Itis a degree less than the one afforded
by such cases as Hveres argiades and F. aleetas, or Polyommatus icarus
and Ayriades thersites, which are ‘twin species,’ and in the second
“twin genera.” (R. Verity.)
Subgroup 0.
Hrebia epiphron, Knoch. |‘ Harz Mts., in Germany.” |
(a) race amplevittata, Vrty., H.R., 1921, p. 211.—Tuscan Apen-
nines and Apuane Alps (“ Mt. Sumbra, 1600m., in the Apuane
Alps,”’ and Alpe Tre Potenze, 1650m.).
(a) race cassiope, F., Mant., 42 [‘* Austria’’].—C.It., further south
than Tuscany, from 1600 to 2000m.
Group I.
Hrebia ceto, Hb. [‘* Glacier region in Switzerland.’’]
(a) race abetonica, Vrty., ’.R., 1919, p. 124.—Tuscan Apennines
(“« Mt. Majori, 1500m., and Abetone Pass ’’).
(b). race obscura, Ratzer, Mitth. Schiv., 1890, p. 222 [‘‘ Switzerland’’| .
— C.It., further south than Tuscany, from 1400 to 1700m.
Group III.
Erebia aethiops, Esp. [‘* Frankonia, in Germany.’’|
(28) THE ENTOMOLOGIST’S RECORD.
(a) race apuana, Vrty., H.R., 1923, p. 185.-— Apuane Alps (Acqua
Bianca, 1300m., on Mt. Pisanino),” in the N.-W. of Tus-
cany, only just within the boundaries of this region.
Note.—Roeei (Memorie Soc. Knt. Ital., March, 1923, p. 7), describes
a very large race from the Ligurian Apennines (‘“‘ Val Brevenna in
the Alta Valle di Scrivia, 600 to 700m. ”), under the name of magna.
Group IV.
Subgroup a.
Erebia yorge, Esp. [‘ Region of Geneva.’’|
(a) race erynis, Esp. trans. ad carboncina, Vrty., E.R., 1921, p.
212.—Apuane Alps (‘‘ Mt. Pisanino, 1200m.”).
(6) race carboncina, Vrty., Soc. Ent. It., 1916, p.54.—C.It., further
south than Tuscany (‘ Fonte Pescolla, 2000m., in the
Sibillini Mts.’’).
Hrebia glacialis, Esp. [*‘ Southern peak of a glacier towards
Chamonix.”’|
(a) race pluto, Kisp., Hur. Schmett., Suppl. IL., p. 19, pl. 121. f. 1
(1805 ?) [‘Col de Chalenton, on path from Mt. Buet to
Faucigny”] or duponcheli, Obthr.—Gran Sasso in the
Abruzzi.
Note.—Calberla in ris, 1887, p. 185, states he found this species on
the Gran Sasso in the Abruzzi, from 1600 to 2200m., with its forms
alecto, Hb., and pluto, Esp. Staudinger, in his Cataloy, gives “‘ the
mountains of Central Italy” as a locality for pluto. My collection
contains one male collected by Dannehl, on the Gran Sasso, on July
24th, 1907. It is exactly similar to Esper’s figure by its rather small
size, elongated wings, tinge not saturated, but brownish, with a shiny
surface ; not the slightest trace of fulvous on either surface. I also
have a male from Mt. Lago, in Western Liguria, collected by Col.
Parvis ; this is larger, has broader wings, and is of a very deep black
on either side; it,no doubt, is race duponcheli, Obth. (Bull. Soc. Ent.
France, 1897, p. 290), described from the Basses Alpes, and it agrees
with specimens from Larche I possess; it is very likely the Abruzzi
race is the latter, but one cannot ascertain this without females which
exhibit the distinctive characters. Calberla has evidently found speci-
mens which are not pluto, but have eye-spots on forewings, as he calls
them alecto. This is the name which is generally used for this form
on the strength of Hubner’s fig. 528-9, but Turati has discussed this
subject thoroughly (Atti. Soc. It. Sc. Nat., LIII. (1914), and concluded
that Hitibner’s first figures of alecto, 515-6, represent a male of the
species usually called nerine, Frr., so that it should replace the latter.
Ksper’s name of persephone |< Mt. Vergy, near Faucigny ’’| seems to
be the one which should be used, for the form of glacialis, wrongly
called alecto. (R. Verity.)
Subgroup 6.
Hrebia tyndarus, Ksp. [‘*On the way of the Grindelwald, near Schei-
deck, in the Canton of Berne.”
(a) race tusca, Vrty., Soc. Hint. /t., 1914, p. 148 and p. 218, t. L., f
17-20.—Tuscan Apennines, from 1300 to 2000m. (‘ Abe-
tone Pass, 1300im.).
(6) race majellana, Frtihst., Soc. Ent., 1909, p. 184 (name given to
- SEASONAL POLYMORPHISM, (29)
Oberthiir’s description of the race from ‘‘ Majella Mt., in the
Abruzzi,” recorded by him under that of cleo, Hb.) (=
infrargentea, Vrty., W.R., 1919, p. 125 (“* Bolognola, 1200m.,
in Sibillini Mts.’’)-—C.It., further south than Tuscany, from
1400 to 2200m.
Group V.
Subgroup a.
Erebia neoridas, B. [‘* Dauphiné, Provence and Lozére.”’|
(a) race sibyllina, Vrty., Soc. Int. It., 1914, p. 236.—“ Sibillini
Mts., 1300 to 1400m.”’
(b) race etrusca, Vrty., The Kutomoloyist, 1904, p. 55, t. 1V., f. 6-8.
Apuane Alps (Mt. Matanna, 1400m.’’), and Alta Valle
Fioio, in the Abruzzi, whence Verity possesses specimens
collected by Rostagno.
Subgroup ec.
Erebia goante, Hsp. [** Thalalpen above Lucerne, in Switzerland.’’]
(a) race apenniniyena, Vrty., H.R., 1918, p. 124.—Ligurian
(Colle di Arpetto’’) and boundary of Tuscan Apennines
(Balzo alla Rosa, 1700m., where specimens were collected by
Costantini).
Erebia pirene, Hb. [No text to figure” (=pyrene, Ksp.—< Tyrol
and Swiss Alps”? =stygne, O.—‘ Tyrol and Swiss Alps.’’)]
(a) race etruriae, Vrty., H.R., 1919, p. 124 (‘‘ Abetone Pass’) (=
costantine,. “Urti., Atée Soc lt. Sc. Nat, 1919; p. 166: “Mt.
Cimone from 900 to 1800m.’’).—Tuscan Apeinines and
Apuane Alps, from 900 to 1800m.
(b) race riihli, Frihst., Soc. Mnt., 1909, p. 124 = pyrenaica, Rubl.,
Gross-schimett., p. 489 (1895) [‘* French Western Pyrenees ”’|
(nomen praeocc.).—Abruzzi, from 1600 to 1800m. (Castel del
Monte in Verity coll.).
(c) race tetrica, Vrty., M.R., 1928, p. 186.—* Sibillini Mts., at
1400m., in the Marche.”
Group VII.
Hrebia medusa, Schiff. [‘* Vienna.”’|
(a) race hyperapennina, Trti., Atti Suc. It. Sc. Nat., 1919, p. 165
(Mt. Cimone, 1500 to 1800m., on northern boundary of
Tuscany ’’).—lecorded from these mountains also by Calberla
and collected at the Abetone Pass by Verity, but hitherto not
observed further south,
Subfamily : Melanargtinae.
Melanargia arge, Sulz. (‘‘ Kingdom of the Two Sicilies.’’)
(a) race turatii, Rost., Soc. Zool. It., 1909, p. 283.—‘* Rome,
100m.”’
(b) race cocuzzana, Stauder, Zeitschr. wissensch. Insektenb., 1914,
p. 875, fig. 12-15.—““Mt. Coeuzzo” and 8. Fili, 500m., in
Calabria.
Note.-—Stauder evidently did not know of the existence of race
tuwratit, when he described his cocuzzana. The latter comes very near
(80) THE ENTOMOLOGISE’S RECORD.
the former, but, as the Calabrian race is not quite so extreme in
character as the nymotypical twratii of Rome, Stauder’s name need
not be sunk in synonymy.
(c) race arge, Sulz.—Neapolitan district (Sorrento, on sea shore ;
Formia, from sea shore to 100 m.; Spigno Saturnia, 1000m.
on Aurunci Mts.; Mt. Vulture, 900m., in Basilicata).
Melanargia russiae (Ksp.) Cyr. — [* Sebastianofka and Pensa in
southern Russia.” | (=specifically japyyia, Cyr.)
(a) race japygia, Cyr., Hnt. Neap., I., tav. II., f. 5 (1787).—Prov.
of Lecce and Benevento, up to 800m.
(b) race medioitalica, Vrty.. Soc. Hnt. It., 1918, p. 216, pl. 1.,
f. 12-18.—* Sibillini Mts., at 1400m., in the Marche.”
Note.— Kirby very rightly uses Esper’s name as the specific one.
There is no reason to neglect it.
Melanargia galathea, Lu. {Germany and more Southern Europe.”
Type Petiver’s figure in Mus., 38, n. 804, plt. L., fig. 3.]
(a). race monticola, Vrty., 17.R., 1919, p. 125.—C.It. in cold local-
ities (“* Firenzuola, m. 400’).
(6) race florentina, Vrty., H.R., 1919, p. 125.—Florence (“ Pian di
Nugnone, 100 to 800m”’).
(c) race sciritis, Frihst., Soc. Mnt., 1916, p. 88.—* Sabini Mts.,
near Rome.”
(d) race microprocida, Vrty., H.R., 1919, p. 125.—*: Benevento,”
160m., and S. Pietro Avellana in (Southern Italy).
(e) race galinthias, Fruhst., Arch. fiir Naturgesch., 1916, p. 21.—
‘“‘ Naples ” and Neapolitan Apennines, up to 500m.
(f) race calabra-procida, Vrty.—Herbst., E.R., 1921, p. 212.—“ 8.
Fili, 500m., on Coast Range of Calabria.”
(g) race calabra, Vrty., Soc. Hnt. It., 1913, p. 215, t. I., f. 9-11.—
‘« Aspromonte, from 700 to 1200 m., in Southern Calabria.”
Subfamily: Satyrinae.
Note.—It is much to be regretted that the generic names, which
are now commonly in use in this subfamily, should have been intro-
duced quite wrongly. Thus the “‘ type-species ”’ of the genus Satyrus,
Latr., being maera, L., this name should be used, as by Kirby and
Bingham, for this species and for meyera and other near allies, which,
according to modern views, must be separated generically from aegeria,
the ‘‘type-species” of Pararye, Hiibner. I have no possibility of
verifying whether Bingham is right in using the name of Nytha,
Billberg, (the “ type-species”’ he states is hermione, Li.) for that section
of the genus usually called Satyrus, which most authors now agree
must be separated from the Hipparchia, as characterised by semele, L.
T use it here on his authority. This correction of the generic names
makes it necessary to change that of the tribe Satyridi into Nythidi,
to obviate hopeless confusion. (R. Verity.)
. Tribe: Parargid?.
Satyrus megera, Li. [‘* Austria and Denmark.”’|
(a) race praeaustralis, Vrty.—I. gen. praeaustralis, Vrty., H.R.,
1922, p. 214; II. gen. paeninsulitalica, Vrty.. H.l., 1928,
p- 24; III. gen. paeninsulitalica, Vrty.—P.I1t., up to 1300m.
(‘‘ Pian di Mugnone, m. 200, near Florence’’).
SEASONAL POLYMORPHISM. (81)
(b) Secondary aberrative race tigeliiformis, Vrty.—I. gen. presum-
ably praeaustralis, Vrty.; Il. gen. tigelitformis, Vrty., Soc.
Ent. Ttal., 1911, p. 269; Ill. gen. tigelitformis, Vrty.—C.It.,
up to 700m., in extremely parched localities (‘‘ Piteglio,
m. 700, in Tuscan Apennines’; Quercianella, on coast,
south of Leghorn).
Note.—Stauder remarks that the specimens he collected on Mt.
Martinello in Calabria and on Mt. Faito on the Sorrento peninsula
come very near the Sicilian and the North African examples. He
evidently says this on account of the superficial resemblance of the
upperside, as these races had not been defined before my paper in
the Mnt. Rec., l.e., but this similarity is very unlikely. My specimens
from the Coast Range of Calabria quite belong to race praeaustralis.
Instead, it is very probable that in the southern parts of Calabria, as
in many other species, there exists the Sicilian race :—
(c) race australis, Zeller.—I. gen. australis, Zeller, Isis, 1847, p.
140 [‘* Messina’’|; II. gen. tigellyssa, Vrty., V.R., 19238, p, 27
[‘‘ Ficuzza’’]; ILL. gen. tiyellyssa, Vrty.
Satyrus maera, L. [‘* Sweden.’’|
(a) race appennina, Vrty.—I. gen. appennina, Vrty.; II. gen.
appennina, Vrty., Soc. Hnt. It.; 1911 jp. 269.—C.It., up to
1300m. (‘‘ Piteglio, m. 700, in Pistoiese Apennines’).
(b) race silymbria, Fribst., Intern. Hnt. Zeit. Gitben, September,
1909, p. 184.—Mt. Faito, on the Sorrento Peninsula, accord-
ing to Stauder, who says that a pair he collected of the I.
gen. is identical with the “types” of silymbria, collected by
himself at Spalato in Dalmatia.
(c) race herdonia, Fruhst., Int. Ent. Zeit. Giiben, September, 1909,
p. 188 [* Arcine in Savoy’’].—S. Fili, m. 1000, on the
Calabrian Coast Range. The specimens of the I. gen.
collected by Querei are quite similar to those of the Maritime
Alps and very different from appennina.
(/) race polsensis, Stauder, Zeit. wissenschaft. Insektenbiol., 1916,
p. 61.—In the river-bed of the Buonamico, at 1100m., on
Aspromonte in Southern Calabria.
Note.—This race of southern Calabria seems to be, according to
Stauder’s description, intermediate between the preceding of northern
Calabria and race sicula, Stdgr., of Sicily, as might have been expected.
Pararge aegeria, L. |‘*More Southern (australioris) Hurope and Mautri-
tania’. This habitat is what establishes the nymotypical subspecies,
as lately accepted generally, because, otherwise, Linnaeus’ first quota-
tion (Réaumur’s figures, pl. 27, fig. 16-17) would refer to a northern
race. |
(A) Subspecies aeyeria, Li. :—
(a) race aeyeria, L., Syst. Nat., ed. X., p. 478 (1758).—Piani di
Carmelia, m. 1200, on Aspromonte Mass in southern Calabria,
collected by Querci on July 21st, 1914.
(Bb) Subspecies vulyaris, Zeller, Isis, 1847, p. 148 :—
(a) race ttalica, Vrty.—I. gen. ttalica, Vrty., Soc. Hint. [t., 1915, p.
55, and H.l., 1916, p. 167 (‘‘ Florence”); IIL. gen. italica,
Vrty.; ILI. gen. ttalica, Vrty.—P.It., up to 1300 m.
(6) race canloenaeformis, Vrty.—I. gen. italica, Vrty.; Il. gen.
camoenaeformis, Vrty., .f., 1919, p. 127 ( Tuscany ’’); IIT.
(82) THE KNTOMOLOGIST’S RECORD.
gen. camoenaeformis, Vrty.—P.1t., in particularly hot and
rather damp surroundings (Isle of Elba at Pozzio, 400m. ;
Springs of Fiugegi, 700m., near Rome).
Note.—I have pointed out in the Hnt. Rec., 1919, p. 127, that the
bright fulvous characteristic form of ttalica is found at all seasons and
in all localities mixed with forms I have named eleyantiaeformis,
camocnaéformis and egestasiformis, that it is more frequent in the early
spring and in late autumn, and that camoenaeformis, the very dark form,
occurs more often in hot seasons and localities, but I have concluded
that none of these forms prevails enough to apply these names to
generations or races. I have since found that in the localities men-
tioned above camoenaeformis is quite constant and racial. From
Liguria and Tuscany to northern Calabria we have otherwise met with
the same forms. I have also discussed the name intermedia of various
authors and concluded it does not belong to Weismann, as stated
by Seitz, or exist in Liguria, nor does it apply to any form of Penin-
sular Italy, except southern Calabria, where, no doubt, a really
transitional form to subspecies aeyerta must exist, together with the
latter, as in Sicily. I have not yet been able to find out the first
description of intermedia, which Ruhl mentions in his Pal. Gros-
schmett, p. 581, without quoting its author; the locality of Naples he
gives evidently is drawn from Zeller, and apples to vulyaris,
which Ruhl mixes up with intermedia, so that the Rumanian
localities presumably refer to the latter. Calberla, followed by Ruhl,
says that Zeller in /s’s, 1847, p. 148, has named vulgaris the race of
Naples, transitional to aeyeria. This is quite a mistake. Zeller uses
that term to designate all the races from Germany to Naples (the
meaning of it would be a sufficient proof in itself) and to contrast them,
as a whole, to the aegeria of Sicily, which he calls meone, Hsp. This is
the very distinction I have made in late years and I think Zeller’s
name should be revived; Staudinger’s later name everides of 1871 can
remain for one of the German vilyaris races in particular, which
Zeller calls “ our aegeria ”’ to distinguish them from the vulgaris of
Naples, described by him as exhibiting characteristics transitional to
meone. I must insist on the point that the very bright fulvous of
italica is the only point of resemblance. eal transitions from vulyaris
to aegerta are alone found in Sicily, and presumably in southern
Calabria. (R. Verity.)
Tribe: Nythid?.
Enodia dryas, Scop. — [‘‘ Carniolia.’’ |}
(a) race julianus, Stauder, Soc. Adriatica Scienze Nat., 1911, p. 117,
pl. ILI, f. 1-2 (Gorizia, from Coglio to Udine).-—C.It., up to
300m. (Baths of Lucca; Rome, according to Rostagno).
Nytha cordula, F. [* Italy’? (Dr. Allioni).]
(a) race calabra, Costa, Mauna Reyno Napoli, t. 8, f. 1-2 (* King-
dom of Naples”) (=acteina, Obthr., Ht. Lép. Comp., UL,
p. 280. ‘‘ Majella, Roccaraso and Palena in the Abruzzi ’’).—
P.It., further south than Tuscany, from 1200 to 1800m.
Nytha statilinus, Hufn. [* Berlin.” }
(a) race apennina, Z., Isis, 1847, p. 184.—C.It. in some mountain
localities (‘at considerable altitudes above Foligno, in
SEASONAL POLYMORPHISM. (33)
Umbria’’; Piteglio, 700m. in the Tuscan Apennines; Piano
Astore, 1200m., in Sibillini Mts.
(b) race intermedia, Vrty., Soc. Ent. [t., 1911, p. 270, and 1918,
p. 215.—C.It., up to 900m. (‘‘ Vallombrosa, 900m., near
Florence’’). This is the most broadspread race in this
region.
(c) race micromarituma, Vrty., H.R., 1919, p. 128.—C.It., up to
500m.,indamp surroundings and especially on coast (‘‘ Forte dei
Marmi, on sea shore, in the Prov. of Luccea;”’ Isle of Elba;
Mollarino valley, in the Mainarde Mts. (Caserta).
(d) race crassemaculosa, Vrty., Soc. Ent. It., 1916, p. 189 (December
1916), and #.R., 1919, p. 129.—*Tsland of Tino, on the Gulf
of Spezia, in hot, moist and shady locality.”
(e) race australis, Z., Isis, 1847, p. 184 (‘‘ type: Hsper’s figure,
pl. CV., f. 4; text in Supplement I., 1, p. 67: sent by the
King of Sicily.) —vestagnor, Vrty., HR, 1919) p: 128 =—
maritima, Rost., Soc. Zool. It., 1911, p. 71 (nomen
praeocc): ‘‘ Formia (Caserta) on sea shore.’’—Querci eol-
lected Rostagno’s ‘‘types”’ in the latter locality. We know
of no other, except Genzano, near Rome, Palermo in Sicily,
but presumably widespread in Southern Italy.
Nytha fagi, Scop., 1768. [‘‘Carniolia”’] (=hermione, L., 1764, ‘* Ger-
many” ; =aleyone, Schiff., 1776, ‘ Vienna’’).
(A) Subspecies fagi, Scop. :—
(a) race latevittata, Vrty., Soc. Ent. France, 1911, p. 312, pl. L., f.
7-9.—C.It., from 900m. to 1200m. (‘Alpe della Luna,
1000m.,” and Mt. Pratofiorito, 1000m., in the Prov. of Lucca ;
Sasso di Castro and Vallombrosa in ‘the Prov. of iloconcer:
Sibillini Mts.
(b) race genava, Fruh, [* Valais.”|—Aspromonte, 1200m., in
Calabria.
(B) Subspecies major, Esp. :—
(a) race alcyoneformis, Vrty., Soc. Hnt. France, 1911, p. 812, pl. L.,
f. 5-6.—C.It., from 500m. to 1000m. (‘Alpe della Luna,
1000m., in the Proy. of Lucca,’ and Mainarde Mts., from
500m. to 1000m., in the Prov. of Caserta.)
(b) race major, Ksp., Hur. Schmett., I., p. 116, pl. VIII. (no locality
given).—C.It., up to 1000m.
Note.—None of the original descriptions of fagi, hermone or alcyone
furnish any clue as to which of the two subspecies they were drawn
from; they all three apply to both. Esper was thus at liberty to
restrict them to either, and he did so by separating the larger one
under the name of major. As he was the first to distinguish them,
this name must be used and that of hermione, which had got into
current use for it, without any reason to support it, must be dropped.
In the Linnean Soc. Journ. Zool., 19138, p. 188, I have pointed out that
the Linnean specimen belongs to the smaller subspecies. Concerning
their relationship see my Note on page 27 on the similar case of Krebia
ligea and philomela. My series from the Aspromonte, in Calabria,
exactly resembles my specimens from Martigny in the Valais, panich if
take to be race yenava, Frihst. (R. Verity.)
(84) THE ENTOMOLOGIST 'S RECORD.
Nytha circe, FE. [Type: figure of Roesel Insecten Belustingung, IV.,
pl. 27., f. 8-4, “ Germany.”’]
(a) race itala, Vrty., H.R.,.1919, p. 129 (« Florence.”)—P.It., up
to 1300m.
Tribe: Hipparchiidi.
Hipparchia neomiris,God. [“ Corsica.’’]
(a) race neomiris, God.—Isle of Elba, from 400m. to 700m.
Hipparchia semele, L. — [** Sweden.’’|
(a) race teres, Frihst., Intern. Entom. Zeit., 1908, p.10. [‘ Digne
in the Basses Alpes.’’}-C.It., in cold and damp surround-
ings, up to 1000m. (Mt. Prato Fiorito, 1000m., near Lucca ;
Mt. Conca, 400m., and other localities near Florence).
(6) race aristaeus, Bon., Mem. Acc. Torino, 1826 (paper read in
March, 1824), p. 177, t. 2, f. 1. [‘* Sardinia.” ] —Isle of Elba,
up to 700m., and Isle of Giglio (Verity coll.).
(c) race apenninigena, Vrty., E.R., 1928, p. 156.—C.It., at very
high altitudes, in alpine surroundings (“ Sibillini Mts., 1200m.,
in the Marche”’).
(d) race cadmus, Frihst., Intern. Entom. Zett., 1908, p. 10
[(‘* Klausen, in 8. Tyrol’’?].—Mt. Sumbra, 1200m., in Apuane
Alps (N.-W. of Tuscany).
(e) race paeninsulitaliae, Vrty., H.R., 1924, p. 24.—P.It., in hot
and dry surroundings, up to 1200m. (‘‘ Mt. Fanna, 600m.,
near Florence’ ; Aspromonte, 1200m., in Calabria).
Hipparchia briseis, L. [ Germany.’’]
(a) race deminuta, Fruhst., trans. ad meridionalis, Stgr., Stett. e. Z.,
1886, p. 242.—C.It., in hot and dry surroundings (Mt. Fanna,
600m. above Fiesole; Oricola, 800m., in the Abruzzi).
(b) race deminuta, Frihst., Intern. Entom. Zeit,, 1908, p. 194.—
C.It., in cold and dry surroundings (‘‘Consuma Pass, 1000m.,
in the Prov. of Florence [and Malser Heide, in 8. Tyrol]”’ ;
Mainarde Mts., 1500m., in the Prov. of Caserta).
(c) race deminuta, Fruhs., trans. ad interjecta, Vrty.—C.It., in low,
cold and damp surroundings (“ Mt. Conca,, 400m., near
Florence ’’).
(d) race interjecta, Vrty., E.R., 1919, p. 129 [‘*Charente, in
France ’’].—C.It., in alpine surroundings (Sibillini Mts.,
1200m., in the Prov. of Macerata).
Family: Libytheidae.
Libythea celtis, Laich. [‘* High road at Unteratzwang, between Brixen
and Botzen, in 8. Tyrol.’
(a) race celtis, Laich.—C.It., (Sibillini Mts., 1200m., in the
Marche ; Atina, 500m., in the Prov. of Caserta).
Family : Apaturidae.
Subfamily: Apaturinae
Tribe: Apaturidi.
Apatura ilia, Schiff. [‘* Vienna.”’]
(a) race eos, Rossi, Mant. Insect. Etruria, p. 9 (1794). No descrip-
tion ; following figures simply quoted. [Types: Figures of
SEASONAL POLYMORPHISM. (35)
Ernst et Engramelle, Papillons d’ Europe, pl. 81, f. 63, a, b,
u; pl. 70, f. 86, a, and of Schaef., Ic. Insect. Ratisbonam, pl.
152, f..8. ‘ Regensburg, in Germany.’’].—I. gen. eos, Rossi ;
II. gen. eos, Rossi.—C.It., up to 200m., (Northern Tuscany
(Florence, beneoh Pietrasanta) ; Acquatraversa near Rome,
observed by Querci.) Local and erratic in appearance from
year to year. Usually along streams shaded by poplars and
willows,
Tribe: Charaxidi:
Charawes jasius, L. [‘ Barbaria (= Algiers), in Northern Africa.’’]
(a) race septentrionalis, Vrty.—I. gen. brevicauda, Vrty., E.R.,
1919, p. 179; Il. gen. septentrionalis, Vrty., Linn. Soc. Journ.
Foal. 1918, p. 180.—P.It., up to 500m. In Tuscany stray
individuals are met with anywhere (we know of three
observed near Florence), but its haunts, where it breeds
abundantly, are the brushwoods of the Maremma, along the
west coast, from Leghorn southwards. Common also round
Lucca and in the Isle of Elba. The second generation
emerges from August 10th to 20th.
Family : Nymphalidae.
Subfamily: Limenitinae.
Tribe: Limenitidi.
‘Limenitis camilla, L., 1764. [“Germany.”] (=sibilla, L., 1767
[Germany ”], et auctorium).
(a) race angustefasciata, Streckf., Berl. Ent. Zeit., 86, 8.B., p. IX.
[(‘‘Carniolia ”] (=steniotaenia, Honr.).—C.It., up to 500m.
(between Pisa and Leghorn; Rome; Atina (Caserta)). Hx-
tremely local.
Limenitis rivularis, Seop., 1763. [“‘ Carniolia’”’ (=camilla, auctorium
nec., L., =drusilla, Bestr., 1779).
(a) race atari Scop.—l. gen. primigenia, Vrty.; I. gen. rivula-
ris, Scop. ; Ll. gen. prodiga, Friihst., Ent. Zeit. Guben, 1909,
p- 94 [es Savoy, Saléve, Pralognan my .—C.It., up to 1300m.
Note.—The first generation differs markedly feor the successive
ones by its smaller size, more slender build, more elongated and pointed
wings, and by the white spaces being distinetly less extensive. On
account of this last character I have of late used the name of reducta,
Stdgr., to designate it, but I think it very unlikely that this name can
suit it well, having been created for an oriental race, so I now propose
that of primigenia, mihi, taking as “types” a series from Florence
in my collection. (R. Verity.)
(b) race herculeana, Stich., Seitz. Pal. Gr.-Sch., I., p. 183, t. 57
[‘* Gravona, in Dalmatia,” and Digne in Southern France] .—
I. gen. primigenia, Vrty.; II. gen. hercwleana, Stich.; III.
gen. prodiga, Friihst.—Prov. of Caserta (Formia on the sea
shore, and Atina, 500m., in Mainarde Mts.).
(36) THE ENTOMOLOGIST’S RECOKD.
Subfamily: Vanessinae.
Tribe: Melitaetdt.
Melitaea aurinia, Rott. [Type: Description of Geoffroy, Abr. Insectes,
Ts pio << Pansy 4
(a) race aurunca, Trti., Ent. Zeit., 1910, p. 223.—F raine, 700m.,
and snow pits of Mt. Petrella, 1300m., in the Aurunci Mts.
(Caserta).
Note.—This little colony of the species, which survives in a spot
hundreds of miles away from its kind, and is not found along the main
chain of the Apennines, is most remarkable. ‘The nearest locality
known is the extreme west of Liguria. Specimens I possess, collected
by Turati in June, at Ceriana, 870m. above S. Remo, are quite similar
to some provincialis, B., from the coast of the Alpes Marit. depart., and
awrunca differs very little from these two. (R. Verity.)
Melitaea trivia, Schiff. [‘ Vienna.”’]
(a) race not identified because the J. gen. is unknown; II. gen.
nana, Stdegr., Cat..Lep. Eur., II. ed. (1871), p. 18. [Original
description: ‘‘minor’’; habitat: ‘Southern Huropean
Turkey, etc.”’; quotation: Esper, pl. 88, f. 5-6 (Sarepta) |] .—
Oricola, 800m. in the Abruzzi, in Rostagno coll.; Verity
possesses it from Genzano, 600m., near Rome.
(b) race not identified because the I. gen. is unknown; II. gen.
nana, Ster., trans. ad catapelia, Ster., Stett. e. Z., 1886, p.
231.—Paliano, 500m., in the Proy. of Rome.
(c) race catapelioides, Stauder.—l. gen. catapelioides, Stauder.,
Zeit. Wissensch. Insekten., 1918, p. 57; IL. gen. is unknown.
—Above “ Paola, from 400m. to 600m.,” and 8. Fili, 900m.,
in Calabria. According to Turati trivia exists also at S.
Lucca, above Reggio.
Melitaea didyma, Esp. [Fur. Schmett., 1., p. 865, pl. XLI., f. 3 (1777) :
“ Frankonia’).
Note.—The races and generations of Peninsular Italy, as drawn out
below, plus meridionalis, Stdgr., of Sicily, are obviously a series of
grades along a single line of variation; three of them, however, are
characterised by the considerable extent of grey suffusion in most of
the females, and each of these corresponds, otherwise, to one of the
grades just mentioned. These relationships can be visualised as fol-
lows (from left to right size increases, fulvous becomes more red, spots
become larger) : ;
I. gen. I. gen. I. gen. Tgen4 sil: gen. I]. gen. II. gen. II. gen.
romana, protea, neeraefor., patycosana. caldaria, bosphor. leopardi. romula,
meridto., palustris, apennintg.,
(a) race romana, Calb.—I. gen. romana, Calb., Iris, 1887, p. 182
(‘‘ Monterotondo, 165m., in the Prov. of Rome’’); II. gen.
caldaria, Vrty., Boll. Lab. Zool. Gen. Portici, 1920, p. 59
(*« Pian di Mugnone, 200m., near Florence ’’).—C.It., in very
dry and hot surrounding. '
(b) race protea, Vrty.—I. gen.: early (15, V. to 7, VI.) emergence
protea, Vrty., B. Soc. Knt. Ital., 1916, p. 183 (‘ Pian di
Mugnone, 200m., near Florence”’), and late (20, VI. to 20, VII.)
emergence romana, Calb.; II. gen.: early (VIII.) emergence
SEASONAL POLYMORPHISM. (387)
caldaria, Vrty., and late (10 to 20, IX.) emergence romula,
Vrty., H.R., 1922, p. 12 (“‘ Genzano, 600m., near Rome ’’).
Note.—In the Pian di Mugnone (Florence) this bipartite emergence
of both generations has been so clearly and constantly observed every
year by Querci as to give the impression of four generations. It is
only by breeding one will be able to ascertain whether this is the case
or whether the groups emerge alternately. I have observed the same
phenomenon of a bipartite [. gen. in the Alps, above Lake Maggiore
(Pian Quagegié, 900m.): the I. emergence occurred till June 9th, and
exhibited the dark alpina, Stdgr., features ; on the 18th there began a
IL. with the features of suwbalpina, Vrty.; probably Frtihstorfer’s yeorgi
from the Tessin is the II. generation of this race and not a third one,
as he supposed, and it corresponds broadly in aspect to Esper’s nymo-
typical didyma of II. gen. of Central Europe, and to caldaria and
romula of tbe south. At Atina, 500m., in the Mainarde Mts.
(prov. of Caserta), a protea pointing to romana, emerges from
June 8th to July 14th, and also its Il. gen. has a simple emer-
gence of caldaria. In the same way at Poggio, 400m., in the Isle
of Hlba, there are two simple generations, but here the II. exhibits
different features, especially in the female; it is of the same
pale yellowish fulvous, with no black suffusion at the base, as
in caldaria, but the black spotting is not as variable, reduced in extent
and partly obliterated as in the latter; on the contrary, there are very
complete and regular series of rather large roundish spots of even size,
which recall a leopard-skin; the marginal band is narrow, but con-
tinuous, whilst in caldarta it is reduced to a series of dots, as in
deserticola, Obth., of Africa; size larger than most caldaria. This form
I propose naming leopardata. It is perfectly constant and racial at.
Elba. In Florence it occurs frequently amongst the nymotypical
caldaria. Instead, in the extremely parched locality of Quercianella,
near Leghorn, I bave only found the most extreme caldaria. In the
male sex the difference between caldaria and leopardata is much less
striking. In Florence the September emergence consists chiefly of
form romula, which in size, colouring and extent of pattern is inter-
mediate between the spring and the summer forms.—(R. Verity.)
(c) race palustris, Vrty.—I. gen. palustris, Vrty., E.R., 1919, p.
179 ; Il. gen. unknown.—C.It., in marshes, along the coast
(‘‘ Marina di Pisa’’).
_(d) race neeraeformis, Vrty.—Il. gen. necraeformis, Vrty., Soc. Ent.
Ital., 1918, p. 212; II. gen. unknown.—“ Delianuova, m.
800, on the Aspromonte (end of July)’ and S. Vili, m. 800,
on Calabrian Coast Range.
(e) race patycosana, Trti.—l. gen. patycosana, Trti., Ann. Mus.
Zool. Napoli, 1911, p. 18, and Nat. Sicil., 1919, p. 7, pl. I1.,
figs. 13-14 (December, 1920) (‘‘ Paola, on sea-coast of Northern
Calabria’”’); Il. gen. romula, Vrty.—Southern It., in warm
and damp surroundings.
Note.—F orm patycosana is the largest of the species in Europe; it
is also characterised by its very broad wings in both sexes (when they
The table on page 36 should be corrected as follows :—
II.gen. Il.gen. Il.gen. Il.gen. I. gen. I. gen. I. gen. I. gen. I. gen.
caldaria. bosphor. leopard. romula. romana. protea. neeraefor. subpatyc.
meridion. palustris. apenninig. patycos.
(38) THE ENTOMOLOGIST’S RECORD.
are set, the insect fits into a square rather than a rectangle) and by its
large black spots. The female sex has a usually light whitish ground
colour suffused with grey in the nymotypical form. The couple
fizured by Stauder in Zeit. wissensch. Insektenb., X. (1914), pl. IL,
is not of the most extreme form either in size or pattern and approaches
more palustris. A race similar to Turati’s Calabrian one has
been discovered by Querci this year in the Camaione Valley, a
narrow, damp gorge in the prov. of Lucca (Northern Tuscany).
It corresponds exactly to the “types” I have seen in Turati’s
collection in size, shape and pattern, but the ground colour is of a
clear yellowish fulvous and the spots stand out sharply on it, but
are not as large. The form of female with a grey suffusion over
the ground-colour is very scarce there, whereas 700 m. higher up on
the mountains one finds nearly exclusively the extremely melanic
apenninigena, which is also smaller. The Camaione race I propose
naming subpatycosana. On the sea-coast of the same province I
have found a less highly characterised subpatycosana, which points to
protea by its smaller size and less prominent markings. The end of
June and beginning of July seems to be the time of emergence of
patycosana, whereas protea is much earlier and palustris too. There
seems to be sufficient evidence to conclude that the damp surround-
ings, which produce patycosana or subpatycosana in the I. gen., always
produce romula in the If. and not caldaria: my September speci-
mens from the Camaione have a particularly large spotting and
in the female the ground-colour is of a particularly light whitish tone ;
at Forte dei Marmi they point to caldaria, just as the I. gen. points to
protea. I have collected romula also at Levanto, in Liguria, at the
end of August, on swampy grounds. The I. gen. of my typical series
of romula of the middle of August from Genzano (Rome) is only known
from two females, which seem dark patycosana, transitional to apen-
ninigena, (R. Verity.)
(f) race subpatycosana, Vrty.—I. gen. subpatycosana, Vrty.; LI.
gen. romula, Vrty.—C.It., locally damp surroundings (Cam-
aione Valley, 800m., in province of Lucca and Forte dei
Marmi, on coast).
(y) race apenninigena, Vrty.—I. gen. apenninigena, Vrty., hf.,
1919, p. 179 (Mt. Pratofiorito, m. 1000 and more, above
Lucea”); Il. gen. caldaria, Vrty.—C.lt., at high altitudes. A
single female of this species found in the Sibillini Mts. at
1200m. is a caldaria.
Note.—Dr. Rocci has sent me his specimens of this species from
Liguria to examine. Although they are too few to give a definite
judgment, these races seem similar to those of the Peninsula. At
Genoa at the beginning of July there is a subpatycosana pointing to
protea, with romula pointing to caldaria as IT. gen., just as on Tuscan coast,
at Forte dei Marmt, A: similar vomula is found also at Cella, in
Western Liguria. In the Val Bisagno, at 600m., a protea perfectly
similar to the Florentine one is produced. In the second half of
August at Casella Scrivia, m. 500, on pudding-stone, instead of the
usual limestone of this region, a race identical with my ‘“ co-types”’ of
bosphorana,.Culot, Soc. Lép. Geneve, 1., 2, p. 166. (December, 1906)
[* south: shore of Bosphorus”’], was discovered by Rocci and nanied
roccit by: Turati, Nat. Sicil., 1919 (December, 1920); it 1s on an
average still smaller than caldaria and it differs from it by having very
SEASONAL POLYMORPHISM. (39)
complete and uniform series of black spots, although they are extremely
minute, and by having a continuous marginal band; this form is not
unfrequent individually amongst the caldaria, but Culot’s and Rocci’s
series are very uniform and no tendency to reach the more extreme
caldaria is perceptible. Frihstorfer, Archiv. fiir. Naturgesch, 1917, n.
6, p. 13 (October, 1919), has named euwtitania a series of July from
Peeli of giant size, but ochre-yellow and with very limited black
spotting on the hindwing, similar to Seitz’ figures of pekinensis and
turanica. This may be a I. gen. second emergence of patycosana ;
anyhow, it seems to be a local form of the latter. Curiously enough
race marsilia, Fruh., described from Marseilles, has not been found
in Liguria, whereas Col. Parvis has found in Piedmont (Monferrato) a
race identical with the cotypes in Turati’s coll. It stands by its
features before romana, on a different line of variation from romula.—
(R. Verity.)
Melitaea cinvia, Li. [‘* Botanical Garden of Uppsala in Sweden.’’]
(a) race australis, Vrty., H.R., 1916, p. 128.—P.It , up to 1200m.
(The II. gen. has never been found in this region.)
Melitaea phoebe, Knoch. [** Vienna.’’]
(a) race tnsca, Vrty.—I. gen. tusca, Vrty., HR., 1919, p. 182; IT.
gen. pauper, Vrty., H.R., 1919, p. 182.—P.It., in very dry
surroundings during the development of the II. gen., up to
600m. (‘Pian di Muenone,” 100 to 300m. near Florence).
(b) race emipanper, Vety.—l. gen. unknown; II. gen. empauper,
Vrty., H.R., 1919, p. 182 (=rostagnot, Trti., Nat. Sic., 1919,
p. 2, pl. I1., f. 10-12, published August, 1920).—P.It., in
surroundings which keep damp all the summer during the
development of the II. gen., up to 1800m. (‘* Camaione
valley, 8300m., near Lucca”’).
(c) race phoebina, Trti.—l. gen. phoebina, Trti., Nat. Sic., 1919, p.
20, pl. Il., f. 4-5, published in August, 1920; II. gen.
unknown.—‘‘ On the Aspromonte, above 1400m., in Calabria,
in May,” and §.’Fili, m. 900, on Calabrian Coast Range.
Melitaea athalia, Rott. [Type: Description of Geoffroy, Hist. Abr,
Insectes, I1., p. 45: ‘ Paris.’
Note-—We agree with Reverdin that itis very doubtful whether
the group of southern races he has separated under the name of
pseudathalia, on account of their male appendages, which resemble
very much those of J. dejone, H.-G., really stands to athalia as a dis-
tinct species. Various facts he has observed seem to point much more
to two divergent series, constituting what I have called ‘“twin-
subspecies,” because in the zone where their habitats meet (S. of
France, St. Gall, 8. Tyrol, Gorizia, Feltre, Trieste), in some cases in-
termediate individuals have been found, whereas in others they have
been found together on the same grounds, and keeping perfectly dis-
tinct. Specimens, from the Verity collection, of all the Italian races
from the Alps to Sicily have been submitted to Reverdin and he has
pronounced them: all to be pseudathalia, except the peculiar little
aureliaeformis, Vrty., Soc, Ent. Ital. (December), 1915, p.186, and Fint.
Ree., 1919, p. 198 (figured by Reverdin), from the Venaria Park of
Turin, which flies with pserdathalia and has appendages of athalia, but
modified as in the Asiatic kenteana and pointing distantly to parthente,
whilst to the naked eye its aspect is identical (except perhaps for the
(40) THE ENTOMOLOGIST’S RECORD.
blacker hair of the palpi) with the awrelia, Nick., of Mt. Musine (Turin),
recognised genitalically by Reverdin.
Subspecies pseudathalia, Reverdin, Bull. Soc. Ent. France, 1920, p.
319, and Soc. Lép. Genéve, 1922, p. 24, pl. 1-2: ‘* Southern and
part of Eastern France, Italy, most of Switzerland, Spain.”
(a) race tenuicula, Vrty., H.R., 1919, p. 198.—C.It., at high
altitudes, in alpine surroundings, up to 1800m. (‘ Piano:
Astore, 1200m., in Sibillini Mts,’’). .
(b) race tenuis, Vrty., H.R., 1919, p. 198.—C.It., up to 13800m.
(‘‘ Pian di Mugnone, m. 200, near Florence’’). This is the
most widespread race over the whole hinterland ; it maintains
a very uniform aspect even in localities where other species
produce races different from each other.
(c) race submaxima, Vrty.—lI. gen. submaaima, Vrty.; LU. gen.
tenuis, Vrty. 26, It., in damp localities alone the coast (OE
dei Marmi in prov. ‘of Lucca Ee
Note.—Broadly speaking the following race maxima may be said to
extend all along the coast from Genoa to Calabria, but to be more
accurate one must note that the race of Tuscany, and perhaps that of
Liguria, is not as large, not of such a warm saturated fulvous and not
so heavily marked with black as the most extreme maxima, which pre-
dominate in Calabria and in the Isle of Elba, and it should be
distinguished by the name of submaxima, mihi. At Fortedei Marmi
I have constantly observed every year a second generation from about
August 20th to September 10th, which exhibits the same features as
race tenuis, Showing maxima and tenuis, different as they are, are only
produced by the effect of surroundings on individual development.—
(R. Verity.)
(d) race maaima, Trti., Ann. Museo Zool. Napoli, 1911, p. 19.—
P.It. up to 500m. (‘‘ Paola,” on sea shore, in Calabria; Poggio
500m. in the Isle of Elba).
- (e) race obscura-maxima, Vrty.-Trti., E.R., 1921, p. 213.—“S.
Fili, 500m., on Coast Range of Calabria.”
(7) race obscura, Vrty., E.R., 1919, p. 194.—‘ Altipiano di Car-
melia on Aspromonte, 1200m., in Calabria.”
Melitaea varia, Meyer-Dur. [‘‘ Bundtner Hochalpen in Switzerland.’’}
(a) race varissima, Vrty., Soc. Ent. [t., 1913, p. 210.—C.It. at high
altitudes from 1200 to 1800m. (‘ Sibillini Mts., in the
Marche’; Gran Sasso in the Abruzzi, according to Standfuss
and Calberla).
Note.—Verity has three males collected by Col. Parvis in Western
Liguria in July, 1903; they are labelled ‘‘ Bordighera,’’ but they so
exactly resemble the varia of the Vallasco, in Maritime Alps, that they
must come from a higher altitude in the mountains above that town.
Tribe: Argynnidi.
Brenthis pales, Schiff. [‘* Vienna.’’]
(a) race medioitalica, Trti., Ann. Museo Zool. Napoli, 1911, p. 21.
—‘ Gran S-esso” and Majella in the Abruzzi at 1500m.
Note.—Specimens in the Verity coll., collected by Col. Parvis on
Mt. Lega and Mt. Capelet in Western Liguria, belong to race brogotarus,
Frih., Int. Ent. Zeit. Guben, 1909, p. 182, described from the Col di
Tenda in Maritime Alps.—(R. Verity.)
SEASONAL POLYMORPHISM. (41)
Brenthis dia, L. [‘* Austria.”]
(a) race laetior, Vrty.—I. gen. laetior, Vrty., H.R., 1919, p. 194;
II. gen. flavens, Vrty., H.R., 1919, p. 194; ILI. gen. flarens,
Vrty.—C.lt., up to 1000m.
Brenthis hecate, Schiff. [** Vienna.’’]
(a) race florida, Vrty., H.R., 1919, p. 195.—* Florence, from 150
to 600m.’ This is the only locality we know for this species
in the region we are dealing with.
Brenthis daphne, Schiff. [ Vienna.’’]
(a) race tenuitermaculosa, Vrty., H.R., 1922, p. 14 (‘* Florence ’’).
—C.It., from coast (Forte dei Marmi) up to 1000m. Very
local and chiefly in the gullies of streams.
(6) race nikator, Fruhst., Int. e. Zeit. Guben, 1909, p. 1138
(‘‘ Klausen in 8. Tyrol ”’}.—Calabria up to 1000m.
Brenthis euphrosyne, L. [** Sweden.’’]
(a) race apennina, Stgr., Cat., 1901, p. 85 («« Apennines ’’).—P.It.,
from 500 to 1800m.
Tssoria lathonia, i. [‘* Sweden.’’|
(a) race florens, Vrty.—l. gen. lathonia, L.; II. gen. florens, Vrty.,
E.R., 1916, p. 180; III. gen. florens, Vrty.—P.It. up to
1000m. (‘‘ Vallombrosa and Florence ”’).
(b) race emiflorens, Vrty.—l. gen. lathonia, L.; II. gen. emiflorens,
Vrty., H.R., 1919, p. 195; III. gen. emiflorens, Vrty.—P.It.,
up to 1300m. (‘‘ Baths of Lucca ”’).
Argynnis aglaia, Li. [“* Sweden.’
(a) race appenninicola, Vrty., Soc. Hnt. It., 1914, p. 218, t. L.,
f. 4-5.—P.It., from 700 to 1300m. (‘‘ Abetone Pass, 1300m.,
in Northern Tuscany ’’).
Argynnis niobe, Li, {‘* Kurope”’ ; no quotation. |
(a) race appenninica, Vrty.—Soc. Ent. It., 1914, p. 213—C.It.,
from 1000 to 1400m. (‘‘ Abetone pass, 18300m., in Northern
Tuscany’).
(6) race rubida, Vrty., trans. ad appenninica, Vrty.—Calabrian
Coast Range, 800m.
(c) race rubida, Vrty., Sec. Hnt. It., 1913, p. 214, t. I., f. 8.—
‘“« Aspromonte, 1200m., in Calabria.”
Argynnis cydippe, Li. (1761) (=adippe, L. (1767)). [** Sweden.”
(a) race clarens, Vrty., H.R., 1919, p. 196.—P.It., up to 1400m.
(‘‘ Florence ’’).
Note.—-In the Linnean Soc.’s Journ., Zool., 1918, p. 182, I have
pointed out the fact that there exists no clue in Linneus’s descriptions
or quotings as to what species he had before him when he described
his cydippe, and that the specimen left by him with this name in his
own handwriting is a niobe corresponding exactly to hisdescription. I
had suggested to correct the name on this account, but some English
entomologists have opposed it, maintaining that specimens are not
reliable and that only data drawn from literature should be considered,
so that in this case one can let things stand as Rottemburg and other
early writers made them out. All have agreed, however, that the
older name of cydippe must be used instead of adippe. (R. Verity.)
(42) THE ENTOMOLOGIST’S RECORD.
Argyronome (Dryas) pandora, Schiff. [* Vienna.’’|
(a) race pandora, Schiff.—Isle of Hlba, up to 600m.; Prov. of
Caserta (Formia on sea shore, Aurunci Mts., 600m., and
Atina, 500m.).
Argyronome (Dryas) paphia, L. [‘* Sweden.”’}
(a) race magnata, Vrty., E.R., 1919, p. 196 [* Les Boutardiéres
(Maine et Loire) in France’’|.—P.It. at high altitudes, in
alpine surroundings (Sibillini Mts. in the Marche).
(b) race magnifica, Vrty., H.R., 1919, p. 196.—P.It., up to
1300m. (‘‘ Florence ”’).
(c) race anargyra, Stgr., Cat., 1871, p. 22 (“S. Europe; W. Asia”)
and Horae Soc. Ent. Ross., 1871, p. 63 [Greece, Sardinia,
Cors., Spain] (see #.f., 1919, p. 197).—Isle of Elba, up to
Om.
Note.-—The name of Dryas, drawn from Htibner’s Tentamen and
adopted by Scudder and other authors for the two last species as
separated from the Argynnis proper, cannot stand, because it was given
by Scopoli to a Satyridi and the Rules of Nomenclature allow no
genus to bear a name already in use in any way. Hubner’s other
name of Aryyronome from Verz. bek. Schmett. (1816) would seem to be
the right one.
Tribe: Vanessidt.
Pyrameis cardui, Li. [‘* Sweden.’’}
(a) race carduelis, Cram., Pap. Hwot., t. XXVI., f. EH, F. [Cape
of Good Hope’”}.—I. gen. carduelis, Cram.; Il. gen.
carduelis Cram.—P.It., in damp surroundings, up to 1300m.
(6) race wniversa, Vrty., H.R., 1919, p. 197.—I. gen. universa,
Vrty.; Il. gen. wniversa, Vrty.—P.It., up to 13800m. (“ Flor-
ence ’’).
(c) race inops, Vrty., E.R., 1919, p. 198 [* Sicily and Algeria ’’].
—I. gen. inops, Vrty.; II. gen. inops, Vrty.—P.It., in dry
surroundings, up to 1800m.
Pyrameis atalanta, L. (‘‘ Sweden.’’)
(a) race atalanta, L.—P.It., up to 1300m.
(b) race minutior, mihi.—P.It., in arid localities (“« Quercianella,
near Leghorn ’’).
Note.—-Stichel (Berl. Ent. Zeit., 1900, p. 124 and in Seit’s Gross-
Schmett, p. 199) describes as italica the race he supposes to exist in
Southern Italy as far north as the Albani Mts. and the Abruzzi, with
a transitional one further north. All this is most surprising, for no
such thing exists. All we can say is that from Tuscany to Sicily, in
very arid localities, very small individuals, with the fracta, Tutt, band-
character, predominate, and that individuals with a faded whitish area
on the underside of the hindwings do occur much more often than in
northern countries. Usually, however. there is in Italy only a very
slight tendency to vary more in the direction of these extreme forms,
and we have never seen a single specimen with the blue spots on hind-
wing, described by Stichel. I have observed facts which seem to
suggest an occasional partial second generation.—(R. Verity.)
Vanessa io, L. [‘* Sweden.’’]
(a) race io, L.—P.It., up to 18300m. We detect no difference
between the Italian races and a series from Norrwicken in
SHASONAL POLYMORPHISM. (43)
Central Sweden, in Verity coll. Commonly seen in the
mountains nearby, never in the plains, but near Florence
broods of larvae are frequent in May, although the butterfly
has only been observed in four or five instances during tens
of year’s collecting by Stefanelli and ourselves.
Kuvanessa antiopa, L. [*‘ Sweden.’’]
(a) race major, Hisp., Schmett. Hur, 1., p. 324, t. XXIX., £. 5
[“‘ Frankonia”’] =creta, Vrty., H.R.,1916, p.101 (“ Tuscany’’).
P.It., up to 1300m.
Aglais urticae, L. [‘‘ Sweden.’’|
(a) race turcica, Stgr., Cat., 1871, p. 16. [Southern Balkans,
As. Min.”].—P.It., up to 1500m. Widespread and abundant
in the mountains from 800m. upwards. The butterfly has
never been observed anywhere in the plain, but on two
occasions a brood of larvae has been found in Florence in
May. In Italy the species seems to have a single generation.
Eugonia polychloros, Li. [** Sweden.”’]
(a) race pulchrior, Vrty., H.R., 1916, p. 101 (“ Florence ’’). —P.It.,
up to 1400m., producing also more or less frequently form
polychloros, Li., or form rubens, Vrty., E.R., 1919, p. 199
[‘‘ Lanusei, in Sardinia’’], according to surroundings. This
species only has one generation, according to modern writers,
and it may be so also in this region, but some March indi-
viduals seem surprisingly fresh to have emerged in June.
Polygonia c-album, Li. [‘ Sweden.’’}
(a) race c-album, L.—I. gen. hutchinsoni, Robson, Young Nat.,
1881, p. 110 [‘‘ England’); IL. gen. c-albwm, L.—P.It., up
to 1800m.
Polygonia egea, Cr. {‘‘ Constantinople and Smyrna.’’]
(a) race egea, Or.—I. gen. egea, Cr; II. gen. t-album, Esp.,
Schmett Hur., Suppl. Vol. I., p. 14, t. XCV.,f. 4 [* Mont-
pellier, in 8. France’’].—P.It., up to 1800m.
Note.—In Ent. Rec., 1919, p. 201, I have stated that individuals
very like Cramer’s figure do occur in Italy, contrary to Stichel’s
opinion in Seitz that they do not exist anywhere. The usual form is
the one figured by Esper as vaw-albwin and, if the former is frequent in
the East, the Western race should bear the latter name [‘' Provence,
in S. France”]. Some April individuals are so fresh-looking that it
does not seem possible they can have hybernated.
ADDITIONS AND CORRECTIONS.
Page 3: Hrynnis alceae,Ksp.—Alter this paragraph as follows :
(a) race australis, Z.—I. gen. praeaustralis, Vrty., E.R., 1924,
p. 106 [‘‘Monreale, 800m., near Palermo] ; II. gen. australis,
Z.; IL. gen. australis, Z.—Southern Calabria.
{b) race magnaustralis, Vrty.—I. gen. alceae, Esp.; II. gen.
magnaustralis, Vrty., H.R., 1924, p. 106 (‘ Tuscany’’) ; III.
gen. griseofulva, Vrty., H.R., 1924, p. 106 (“Pian di
Mugnone, near Florence ’’).—Central and probably the whole
of P.It., up to 1300 m.
(44) THE ENTOMOLOGIST’S RECORD.
Page 8: Erynnis altheae, Hb,—Alter: II. gen. australiformis, Vrty.,
into II. gen. fulvipinnulis, Vrty.. H.R., 1924, p. 106
(“ Tuscany ”).
Page 4: Hesperia armoricanus, Obth,—Alter: Ll. gen. fulvoinspersa,
Vrty., into: ILI. gen. and add II. gen. tersa, Vrty., H.R., 1924,
p. 107 (‘‘ Camaione Valley, 400m., near Lueca’’). ;
In very hot localities one meets, not unfrequently, with form
fabressei, Obth., Mt. Lep. Comp., IV. p. 412, fig. 518-520 (1910)
(‘Sierra Alta, in Castile”], but we have never found it to prevail.
In the second half of October in Florence, there occurs in favourable
years an emergence of individuals similar to the spring generation, but
whether they reproduce and thus constitute a IV partial generation,
or not, remains to be established.
Page 4: Hesperia onopordi, Rbr.—Alter I]. gen. fulvotincta, Vrty..,
into III. gen. and add If. gen. terstor, Vrty., H.R., 1924,
p. 106 (“ Camaione Valley, 400m., near Lucca ”’).
Page 5: Urbicola comma, l.—Alter this paragraph as follows :
(a) race aurata, Vrty., H.R., 1924, p. 107.—* Abetone Pass, at
1800m., on northern boundary of Tuscany, on very arid stony
. ground.”
(6) race apennina, Rost., . . . .
(c) race orae, Vrty., H.R., 1924, p. 107.—On coast of C.It.
(“ Pertusola, on Gulf of Spezia, and Quercianella, near Leg-
horn,” Levanto) at a few hundred yards from shore.
(d) race alpina, Bath,
Page 5: Heodes virgaureae, L.—Cancel: Boscolungo
from localities of race apennina, Calb., and add:
(b) race quercit, Trti., Atti. Soc. It. Sc. Nat., 1923, p. 42.—
« Sibillini Mts.”
(c) raceemilianus, Trti.,/.c. [‘‘Hmilian Apennines’’] .—Boscolungo,
1800m., on northern boundary of Tuscany.
Page 6: Loweta dorilis, Hifn.—Alter: I. gen. italorwm, Vrty., into :
I. gen. ttalaveris, Vrty., H.R., 1924, p. 108 (“* Pian di Mugnone,
near Florence ”’).
Page 6: Lycaena arion, L.—Add:
(b) race australpina, Vrty., H.R., 1924, p. 109.—C.It., at high
altitudes, in alpine surroundings (‘ Bolognola, 1200m. in
Sibillini Mtg.’ and presumably Palena and Roccaraso in the
Abruzzi).
(c) race taras, Frhst., Soc. Hntom., 1915, p. 68.—“ Aurunci Mis.
(Valle del Petrella, 1400 m.) in the prov. of Caserta.”
Page 6: Lycaena euphemus, Hiib. and Note to Genus Lycaena on page
18.—The confirmation of the existence of this species in the
Sibillini Mts. in this Note has turned out to bea mistake. Querci
collected (July 10th to 24th) at 1700m., under the Pizzo Tre
Vescovi some females and referred them on the field to
euphemus, but males were subsequently found and they all
turned out to be L. alcon, Schiff., although this race is so
different in the female from any other (Verity possesses an
unusual blue female from Dusseldorf which is transitional to
them) that it needs some attention to recognise the species,
as ath
peakotl ive
ae NEN
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J hohai
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LIST OF THE MACRO-LEPIDOPTERA, (17)
Apamea ophiogramma.—N.F., H.F.C.; Ringwood, N.; Shawford,
f.c., R.; Romsey, Pe.; Winton, c., Ht.
Miana strigilis.—C. ev.
Miana fasciuncula.—Gen. dist., f. ¢.
Miana literosa.—Ch. Fd., r., R.; Romsey, Pe.; Winton, occ., Ht.,
Eee ortsdownc..eb.. Heel. Were nek. Gx
Miana bicoloria.—Gen. dist., c., sometimes abt. ; More on the coast
than inland, Ht.; I.W., Freshw., c., M.; c. and variable, 7.W.G.
Xylophasia rurea.—Gen. dist., more or less c.
Xylophasia lithoxylea.—Gen. dist., more or less c.
Aylophasia sublustris—N.F., Pe., E.R., XVII. 171; Ch. Fd., r., A.;
Winton, occ., M.; Ptsmth., c., sometimes abt., B.; Portsdown, f. c.,
H.; Alton, oce., S.; Monxton, f.c., H.; I.W., St. Lawrence, B. ;
Sandown, Freshw., Shanklin; c. some seasons, 1.W.G.
Xylophasia monoglypha.—Abt. ev.
Xylophasia hepatica.—N.F., sometimes abt., T.; r., B.; Ch. Fd.,
Weal Cs iris: (SOlONsIC. Hck. \Vintoneoccs. Menvkite eb tsmthewtrc.) Ba:
Alton, S.; Gen. dist. in Nth., H.; I.W., well dist., f. ¢., 1.W.G.
Xylophasia scolopacina.—Ringwood, N.; Ch. Fd., 1 sp., A.; sc., R.;
Pamber, c., H.
Dipterygia scabriuscula.—N. F., oce., T., J.; Ringwood, N.; Bnmth.,
Ct.; Bassett, c., A.; Ch. Fd., f.c.,R.; Winton, f.c., Ht. ; Marchwood,
Hikes etsmih, cs B.; Havant, 1 ispsebus) Pamber, Bere, ¢:, HH. :
Sth. of Newbury, SI.; I.W., Freshw., Hnt., 1904, p. 298.
Cloantha polyodon.—1 sp., 1855, M.B.I., I. 282; Occurs, V.
Aporophyla lutulenta.—Bunmth., r.. R.; Bassett, r., A.; Ch. Fd.,
se., R., A.; Winton, 2 sp., Ht.; Harewood, Monxton, Silchester, c.,
H.; I.W.; Freshw., c., M., T., etc.; St. Helens, f. c., B.; Sandown,
Bembridge, Vent., Yarmouth, 1.1V.G.
Aporophyla nigra.—N.¥., Ht., M.; Ringwood, N.; Boscombe, sc.,
R.; Christch., Dt.; Bassett, f. c., A.; Soton, occ., M.; Fareham, 1 sp.,
H.; J.W., St. Helens, f. c., B.; Sandown, Carisbrooke, Vent.,
Yarmouth, Shanklin, in some numbers, J. /V.G.
Aporophyla australis.—I.W., Ht., etc.; Freshw., f. ¢., Pe., T.;
Sandown, #.R., VIII. 220; A fairly plentiful species on the downs,
ete., 1. W.G.
Epunda lichenea.—Christch., oce., M.; Sth. of Newbury, SI].; L.W.,
Hewett, W.B.1., I. 285; St. Helens, larvae occ., 1. W.G.
Polia flavicincta.— Winton, r., W.L., 1891; Occurs, V.; I.W.,
Shanklin, 1 sp., [.WV.G.
Polia chiimOccurs, V.; Christch., H.F.C.; Southsea, Hk.
Brachionycha sphinv.—N.F., n. c., M., B.; Ringwood, N.; Soton,
Pose dee Ae ae Chin hdeweveseh.Ae ae RomseysehensWitonen ray a7.
1891 ; Portsdown, n. c., B.; Pamber, oce., H.; 1.W., Whippingham,
TLW.G.
Miselia oxyacanthae.—Gen. dist., ¢.; var. capucina, oce.
Agriopis aprilina.—Gen. dist., c.
Huplexia lucipara.—e. nearly ev.
Phlogophora meticulosa.— Abt. ev.
Mormo maura.—e. nearly ev.
Naenta typica.—e. nearly ev.
Helotropha leucostigma.—Oceurs, V.;.Christch., Dt. ; Havant, 1 sp.,
H.; LW., Sandown, 1 sp., 7.W.G.
(18) THE ENTOMOLOGIST’ S RECORD.
Hydroecia nictitans.—Gen. dist. and c. in damp places; var. paludis,
usually more c. than type.
Hydroecia micacea.—N.F., n. c., B.; Ringwood, N.; Soton, r., F.;
Bassett, c., A.; Ch. Fd., n. c., R.; Romsey, Pe.; Winton, oce., Ht. ;
Fareham) cf: To; Ptsmth.; nie. B. ;- Havant, ¢), KE.) -Akton, ¢:;S.;
Monxton, f. c., H.; Sth.‘of Newbury, Sl.; I.W., f. c., 1.W.G.
Hydroecia petasitis—Occurs throughout, V.; Hastleigh, 1 larva,
1921, F.; Romsey, 1 sp. by Dr. Buckell, Pe.
Ochria ochracea.—N.F., c., Ht.; Ringwood, N.; Soton, f. ¢., F.,
M.; Ch. Fd., c., Ry, ‘A.; Hursley, oec:, M.; Hastleigh; oce., K.;
Romsey, Pe.; Ptsmth., n.c., B.; Heckfield, 1 sp., T.; Havant, n. «.,
K.; Alton, 8:; Monxton, 1 sp., H.; Sth. of Newbury, Sl.; 1.W:,
sometimes c., I. W.G.
Nonagria spargantt.—Milford, 1. sp., Pe.; I.W., Freshw., r., Pe.,
M.; Nr. Brading, a fair number, J.W.A:.N.S.
Nonagria typhae.—Loce. c. nearly ev.
Nonagria geminipuncta.—OChristch., c., T., R.; Soton, Romsey,
Nursling, Shawford, loc. c., F.; Eastleigh, Winton, c., K.; Havant,
loc. c., H.; I. W., Freshw., c., M.; Sandown, Brading, J.W.G.
Ooenobia rufa-—N.¥., f. e:, M.3 Ch: Kd., Ac; Pismith., nie% sBe:
Shortheath, nr. Kingsley, abt., 1921, S.; I.W., Sandown, vy. loc.,
1.W.G.; Freshw., Pe.
Senta maritima.—Boscombe, R.; Ringwood, N.; Ptsmth. salterns,
1 sp., B.; Havant, n. c., T., Es; 1.W., Freshw., Pe., T.; Sandown, ih
fair numbers, considerable variation, J.W.G.
Tapinostola fulva.—N.F., occ., M.; Ringwood, N.; Soton, n. c.,
F.; Ch: Fd., c., R., A.; Romsey, Pe.; Ptsmth., n. c., B.; Havant;
loc. c., H.; Alton, c., 1920, S.; Andover, Silchester, H.; Sth. of
Newbury, Sl.; I.W., Sandown, J.W.G.
Tapinostola hellnanni.—\.W., Sandown district, 2 sp., 1.W.G.
Calamia lutosa.—Christch., Dt.; 1.W., Freshw., 1 sp., F.R., V. 268;
The Culvers, 1 sp., Freshw., Shanklin, 1 sp., /.W.G.
Calamia phragmitidis.—Christch., Dt.; I.W., Sandown, E.R.,
VIII. 174; Sandown, Shanklin, Luccombe, ab. rufescens also occurs,
T.W:N:H.S.
Leucania pallens.—Abt. ev.
Leucania l-album.—I.W., Sandown, 1 sp., E.R., (901, p. 332.
Leucania favicolor.—Ptsmth., Hayling, 8 or 9 sp., B., Ps.; I.W.,
Sandown, 1 sp., 1895, Freshw., 1 sp., J. W.G.
Leucania impura.—e. ev.
Leucania straminea.—Ringwood, N.; Soton, r., F.; Romsey, Pe. ;
Winton, r., Ht.; Ptsmth., n. c., B.; Havant, loc. abt:, K.; Alton, S. ;
I.W., Freshw., c., T.; Sandown, occ., 1.W.G.
Leucania impudens.—N.F., oec., T., M.; loc. c., B.; Ringwood, N.;
Novon, OCCi eta ALe (Ch Hid-sate Gs hae ametsnah hese (cemelae
Leucania obsoleta.—I1.W., a few in marshes nr. Sandown, I./V.G.
Leucania littoralis—Boscombe, f. c., R.; Bnmth., ¢., V., Dt.;
Ptsmth., c., B.; Hayling, abt., T., E.; I.W., c., V.; St. Helens, abt.,
AW, 1B
Leucania conma.—Gen. dist., usually c.
Leucania putrescens.—Boscombe, v. r., R.; /.R:, XIII. 369.
Leucania unipuncta.—N.F., 1 sp. at sugar, Church Place Enc.,
Oct. 8, 1896, by Rev. G. Hughes of Woolston, Hnt., 1896; M.B.1.,
LIST OF THE MACRO-LEPIDOPTERA. (19)
I. 311; 1 sp., Hnt., XL:, 19138; I.W., Sandown, 1 sp., #.R., 1907,
p. 803.
Leucania vitellina.—Oce. sp., chiefly on or near coast: Christch.,
occ., R., Dt.; Ringwood, N.; Brockt., 1 sp., /.R., 1V. 337; Havant,
1 sp., 1922, K.; I.W., Freshw., oce., Ht. #.R.; Sandown, 1 sp., L.f.,
X. 232; Sandown, Freshw., Bembridge, occ., 1.W.G.
Leucania albipuncta.—Boscombe, r., R.; Ptsmth., Hayling, v. r.,
B.; I.W., Freshw., some numbers, V.; Sandown, occ., H.R., LV. 278,
etc. ; Freshw., f. c:, E.R., V., 1.W.G.
Leucania lithargyria.—Gen. dist., more or less ¢.
Leucania conigera.—Gen. dist., c.
Leucania turca.—N.F., used to be abt., V.; c. at intervals, Ht. ;
loc., J., M., T., Hk.; Bassett, 1 sp., A.; Ptsmth., loc. r., B.; Havant,
1 sp., HE.
Grammesia trigrammica.—Gen. dist., ¢.; var. bilinea, occ. with the
type.
Stilbia anomala.—N.F., loc. f. c., B., A.; Bassett, r., A. ; Baddesley,
r., F.; Oh. Fd., loc..c., R.; I.W., St. George’s Down, I.W.N.H.S.
Caradrina morpheus,—Gen. dist., f. ¢.
Caradrina alsines.—N.F., E.R., 1X. 92; Ringwood, N.; Bassett,
A.; Ch. Fd., c. some yrs., R.; Winton, f. c., Ht.; Ptsmth. salterns,
f.c., B.; Havant, f.c., E.; Gen. dist. in Nth., H.; Sth. of Newbury,
Sl.; I.W., A.; Sandown, Luccombe, nr. Shanklin, n.'c., 7.W.G.
Caradrina taraxacit.—Gen. dist., more or less c.
Caradrina ambigua.—N.F., 2 sp., H.R., XI. 26; Ringwood, N. ;
Boscombe, n. ¢., oe Christch., Dt.; Bassett., r., A.; Southsea, Hk. ;
Hayling, n. ¢., ai W., Ereshw: - some numbers, T., Pe., H.R., V.
268 ; Sandown, = ee E. R VIII. 200, etc.
Caradrina quadripinétata.—Gen. dist.; f. ¢:
Caradrina exiywa.—-Boscombe, v. r., R.; Christch., Dt.; Ch. Fd.,
1 sp., A.; Romsey, 8 sp., Pe.; Ptsmth., 2 or 8 at light, B.; Ptsmth,
1 sp., 1914, Ps.; Swanwick, 1 sp., A.; Havant, 2 sp., 1920, 1922, EH. ;
I.W., Freshw., £.R.; A full account of its occurrence in I.W. is given
in I.W.G., p. 407.
Petilampa arcuosa.—Ringwood, N.; Christch., Dt.; Soton, ¢., F.;
Ch. Fd., f. c., B., A.; Winton, r:, Ht.; Ptsmth, f.c., B-; Purbrook,c.,
T., Ps.; Fareham, 1 sp., H.; Alton, 1 sp., S.; Sth. of Newbury, Sl. ;
I.W., Freshw., c., T.; Bembridge, Sandown, 1 sp., 1.W.G.
Acosmetia caliyinosa.—N.F., v. loc., n. c., M., Ht., A.; Stubby
Copse, 1 sp., H.R, 11. 188; A few localities nr. Brockt., V.; I.W.,
loc. r., A.; Hint., 1920, p. 20; About 20 taken, 1909, 1.W.N.H.S.
Rusina tenebrosa.—Gen. dist. in woody places, ¢
Amphipyra pyramidea.—Gen. dist. in all large woods, ¢.
Amphipyra tragopogonis.—c. nearly ev.
Panolis grisco-variegata (piniperda).—Gen. dist. among firs, often c.
Pachnobia leucographa.—N.F., r., M.; 1 sp., B.; Liss, f.'c., Ps. ;
Burghclere, 1 sp., Sl.; I.W., r. and gee LW:G.
Pachnobia rubricosa.—N.F., f. ¢., T., M., B.; Ringwood, N.; Soton,
f. ci, F:, A.; Ch.'Fd.,'f..c¢., R., A.; Winton, n.c., Ht.; Fareham, n. €.,
T., H.; Portsdown, ¢., B.; Harewood, Pamber, H.; Sth. of Newbury,
S1. ;31.W., Sandown, Cowes, Shanklin, /.W.G.
Taentocampa gothica.—c. ev.
Taeniocampa niniosa.—N.F., f.c.,M., B.; Ringwood, N.; Holmsley
’
(20) HH ENTOMOLOGIST S RECORD.
{ci Re: Sotonsns c. Hoy Ae Chi-Wds i cy han Mt..3) Pismihy ¢59b.5
Fareham, n.c., T. H.; Pamber, H.; Sth. of Newbury, Sl.; 1.W., n.c.,
Parkhurst, Bembridge, East Cowes, I.W.G.
Taeniocampa pulverulenta.—c. ev.
Taeniocampa stabilis.—Abt. ev.
Taeniocampa populeti.cN.F., Ringwood, N.; Ch. Fd., r., RB.;
Romsey, Pe.; Portsdown, sc., B.; Havant, c., E.; I.W., Shanklin,
neice J2WeG,.
Taeniocampa incerta.—c. nearly ev., very variable.
Taeniocampa munda.—e. nearly ev., very variable.
Taeniocampa gracilis.—Gen. dist., not usually c.; Larvae of var.
rufa c. in N.F., on bog myrtle.
Dicycla 00.—N.F., H.F.C., ete. ; v. loc., Ht.; some yrs. abt., rare
in N. F. since 1871, V.; Pamber, 2 sp., 1916, H.
Calymnia pyralina.—Christch., Dt.; Alton, 1 sp., S.; Hants,
MeBeiy il, pase; LW Bembridee nr, TW. G.
Cais Gea Ringwood, N.; Bnmth., f. c., Ct.; Bassett,
1 sp., ms Ch. Fd., Pexecas Eastleigh, Oce., K.. Romsey, Po :
Piamthy Bei eee f. C., Pst: Fareham, H. ; Haeane Cay.
Alton, ¢., ce Monxton, H.; Sth. of Newbury, Sy laws Sandown,
St. Lawrence, Freshw., Bembridge, Kast Cowes, LW.G.
sens difinis.— Ringwood, N.; Bnumth., Ct. ; ae tlerees
i eortsdowur reels) TW... Pannen ee Bembridge,
Bast Cowes, L.W.G.
Calymnia trapezina.—Abt. ev. in woods.
Dyschorista suspecta.—N.F., among birch, Ht.; c. in 1896, Hayling,
MBA., 11.,.p. 73 Ch. Fd;, one, or: two only, R.; Portsdown, r., B.;
I.W., Sandown, 1 sp., 7. W. iG
Dyschorista _fissipuncta.—Christch., ¢., R.; Shawford, c., R.;
Winton, c., M., Ht.; Ptsmth., c., B.; Havant, c., E.; 1.W., Cowes,
I.W.G.
Plastenis retusa.—N.F., f. c., B.; Soton, f. c., F.; Ch. Fd., se., R.;
Fareham, f. c., B.; Horndean, f. c., B.; Westbourne, Sheepwash, c.,
Ps.; Basingstoke, f. c., M.; Nth. Hants, Ht.; Sth. of Newbury, Sl.;
I.W., old records only.
Plastenis subtusa.—Christch., H.F.C.; Ch. Fd., se., R.; Romsey,
Pe. ; Winton, r.; Ht.; Havant, 1 sp., E.; 1.W., Freshw., 'E. Eten Vie
253.
Cirrhoedia xerampelina.—N.F.,loc.¢., J.; Rinegood N.; Lymington,
several, Hnt., LI. 9; Bishopstoke, 1 sp., K.; Romsey, Pe. ; Fareham,
1 sp., T.; Meon Valley, H.F.C.; Amport, occ., M.; Harewood, 1 sp.,
Pamber, occ., H.; Nth. Hants, Ht.
Omphaloscelis lunosa.—Gen.-dist., more or less ec.
Amathes lota.— Gen. dist., ¢.
Amathes macilenta.— Gen. dist. c.
Amathes circellavis.—Gen. dist., more or less c.
Amathes helvola (rufina).—N.F., f.¢., J.. M., B.; Ringwood, N.;
Sotonc:, Hy Aj; Chykds fc; hi Al Romsey Pes Wanton, icy yEt..:
Botley, f. ¢., T.; Horndean, sc., B.; Southsea, Hk.; Harewood,
Pamber, Hyden Wood, abt., H.; Sth. of Newbury, S].; I.W., Sandown,
a few, Yarmouth, f. c., /.W.G.
Amathes l lychnidis (pistacina). —Gen. dist., abt.
Amathes litura.—N.F., ¢., M., B.; Ringwood, N.; Christeb., Dt.;
LIST OF THE MACRO-LEPIDOPTERA. (21)
Soton, sc., F.; Bassett, f. c., A.; Ch. Fd., f. c., R., A.; Romsey, Pe. ;
Winton, Ht.; Horndean, f. c.,B.; Hyden Wood, c., T.; Alton, 1 sp., —
S.; Gen. dist. in Nth., H., Sl.; I.W., Freshw., J.W.G.
Cirrhia citrago.—-Ringwood, N.; Hassett, r., A.; Ch. Fd., 1 sp.
only, ‘‘ miles from lime,” R.; Fareham, n.c., T.: Horndean, r., B.;
Alton, f. c., S.; Monxton, Longparish, H.; I.W., Niton, 1 sp., J. W.G.
Ochria aurago.—Soton, 1 sp., F.R., XIV. 846; Hursley, Ch. Fd.,
Farley Mt., n. c., R.; Crab Wood, r., Ht.; Fareham, 1 sp., T.; Horn-
dean, r., B.; Hyden Wood, Rowlands Castle, n. c., Ps.; Alton, f. c.,
S.; Harewood, sometimes c., Silchester, 1 sp., H.; I.W., old records
only.
Fae lutea (flavago).—Gen. dist., c.
Xanthia fulvago.— Gen. dist., c.; I.W., infrequent, 7.W.G.
Mellinia ygilvago.—Rinegwood, N.; Bassett, 1 sp., A.; Ch. Fd., v. r.,
R. ;, Havant, f..c., E.; Monxton, f. c., H.; 1.W., H.F.C.; Sandown,
2 sp., 1.W.G.
Xantholeuca croceago.—N.F., n. c., M., Ht.; Ringwood, N.; nr.
Lymington, J.; Fareham, occ., T., H.; Harewood, oce., H.; Sth. of
Newbury, r., Sl.; I.W., Parkhurst, I. W.G.
Orrhodia erythrocephala.—Boscombe, I sp., 1902, R.; N.F., Ht.,
M.B.I., Il. 24.
Orrhodia vaccinii.—. ev.
Orrhodia ligula (spadicea).—Gen. dist., usually c.
Dasycampa rubiyinea.—N.F., r., B., M., Hk., J.; Christch, Dt., R. ;
Romsey, 3 sp., Pe.; Nth. Hants, 1 sp., Ht.; I.W., M.B.I., Il. 27;
Rare, /.W.G.
Hupsilia satellitia.—C. ev.
lithophane semibrunnea.—Christch., r., R.; Soton, r.j F.; Ch. Fd.,
4, R., A.; Romsey, ec. some yrs., Pe.; Crab Wood, r., Ht.; Botley,
oee:, T.; Horndean, n.c:, B.; Hevant, 2>sp:, H.; Alton; lysp.. 8);
Monxton, 2 sp., Harewood, 1 sp., H.; Sth. of Newbury, Sl.; I.W.,
old records only.
Lithophane socia.—N.F., f. ¢., M., T., Hk., J.; Ringwood, N.;
Christch., n. c., R.; Soton, f.c., F., A.; Ch. Fd., n.c., R., A.; Rom-
sey, c., Pe.; Eastleigh, oce., K.; Crab Wood, Ht.; I.W., old records
only.
Graptolitha ornithopus.—Gen. dist. in Sth., c.; Apparently se. in
Nth. and in I.W.
Xylocampa areola.—C., ev.
Calocampa exoleta.—N.F., f. c., Ht., M., T.; Ringwood, N.;
Boscombe; 15 Ra; Soton, t.,EAae Ch. Kd. ses, eee Wintonae.. EL.
Horndean, n.c., B.; Fareham, 1 sp., H.; Swanwick, occ., A.; Head-
ley Park, 1 larva, S.; Sth. of Newbury, Sl.; I.W., Freshw., occ., #.R.,
IV. 237, ete.; Shanklin, Sandown, Freshw., in fair numbers, J.W.G.
Calocampa vetusta.—N.F., n. c., M.; Ch. Fd., sc., R.; Horndean,
n.¢., B.; Fareham, | sp., T.; Sth. of Newbury, Sl.; I.\W., Freshw.,
occ., Pe., R.; Sandown, Vent., Whippinghamm, c., 1.1V.G.
Cucullia verbascit.—Gen. dist., n. c.; No record for N.F.
Cucullia scrophulaviae.—Romsey, sc., larvae singly on water betony,
R., Pe. ; a doubtful record.
Cucullia lychnitis.—Bnmth., v. plentiful, £.R., XI. 194 ; Soton, sc.,
F.; Shawford, Winton, r. and loc., Ht., R., M.; Winton, loc. c., A.;
(22) THE ENTOMOLOGIST’S RUCORKD.
Waterlooville, Hk.; Ditcham, c., B.; Clanfield, sometimes c., Ps. ;
Alton, 8.; Sth. of Newbury, SI.
Cucullia asteris—Ch. Fd., uncertain, A., f. c., R.; Romsey, Pe. ;
Hayling, n. c., H.; 1.W., Freshw., Pe. cs
Cucullia wnbratica.—Gen. dist., n.¢.; N.F., Milford, f. c., 1912,
Ct.; No other record for N.F.
Cucullia chamomillae.—-Christcb., sc., R., Dt.; Ch. Fd., r., BR. ;
Winton, 1 sp., W.L. 1875; Swanwick, A.; Ptsmth., n.c., B.; Fareham,
1 sp., T.; Pamber, 1 sp., H.; Sth. of Newbury, SI.; I.W., loc. r., A.
Cucullia gnaphalii.imHants, Ht., Barrett.
Cucullia absinthit.—I.W., Ht., M.B.I., IJ. 48 ; Old records of larvae;
Not seen for many years,
Anarta myrtilli.—Gen. dist. on heaths and commons, more or less c.
Heliaca tenebrata.—Gen. dist. in grassy places, more or less c.; I. W.,
St. Boniface Down, Bembridge, I.W.G.
Pyrrhia wunbra.—Higheliffe, c., A.; Winton, f.c., M., Ht.; Michel-
mersh, f.c., M.; Ptsmth., larvae abt., Ps.; Hayling, c., B.; Nore
Hill, S.; Pamber, 2 sp., 1916, H.; Sth. of Newbury, SI.; I.W., San-
down, c., H.R., V. 274; Vent., Niton, Freshw., Gurnard, Shanklin,
I.W.G.
Heliothis dipsacea,—N.F., loc. c., M., T., K., etc.; Damerham, 1 sp.,
Ct.; Crab Wood, occ., Ht.; Fawley Down, 1 sp., F.; Hayling, r., B.;
Monxton, 1 sp., H.; I.W., Whippingham, 1 sp., 1.W.G.; St. Lawrence,
1 1B)
Heliothis peltiyera.—Fareham, 1 sp., T.; Ptsmth., Hayling, Sheep-
wash, r., larvae f: c., 1920, se. in 1921, B., Ps:; I.W., Vent., 4 sp.,
C.; Freshw., occ., H.R., V. 268, 275, Pe., etc.; Hnt., 1906, p. 288.
Sandown, occ., 1.W.G.
Heliothis armigera—I.W., Vent., 1 sp:., C.; Freshw., 1 sp., T.;
Freshw., occ., H.R., LII1., 288, V. 268, 275, M.B.1., I]. 52; Sandown,
ee Ges
Acontia luctuosa.—Fdge., 2 sp., Ct.; Boscombe, R.; Winton, occ.,
F.; Romsey, Pe.; Ch, Fd., sc., R.; Crab Wood, Hursley, f. c., Ht. ;
Fareham, occ., T., H.; Portsdown, occ., I’., Ps.; Monxton, Longparish,
H.; I.W., Vent., Hk., V.; Freshw., 1 sp., A.; Pelham Woods, San-
down, Brading, Bembridge, J.W.G.
Thalpochares ostrina,—I.W., 2 sp., 1858, 1 sp., 1859; on the Culvers,
MB, U1 55:
Thalpochares parva.—I.W., M.B.I., 11. 56; Freshw., V.
Thalpochares paula—I.W., Freshw., 1872, M.B.1., Il. 56, V.
Hapalotis fasciana.—N.F., n. ¢.. T.; abt., V.; ¢., Ht., J.; Soton,
ch VAG Ch. Wd: nc. "R. A Horndean, se, Ba; |Basmestoke: ni ic.,
M.; Alice Holt, loc. c., 1920, S.; Pamber, c., 1920, H.; I.W., Freshw.,
Bembridge, [.1V.G.; Liphook, f.e.
Hydrelia wneula.—N.F., n. ¢., A.; Ly., Beaulieu, nr. Brockt., c.,
V.; Soton, c., F., K.; Shortheath, 8.; Woolmer, loc. abt., E.; Brams-
bury Common, 2 sp., H.
Rivula sericealis.—N.¥., f. c., V.; Soton, Eastleigh, c., F.; Ch. Fd.,
n. .¢., R.; Fareham, n.‘c., T., Hi; Pismth.,” Purbrook, f: c¢:, B.;
Havant, n. c., E.; Alton, abt., S.; Woolmer, c, E.; Harewood,
Pamber, H.; I.W., Sandown, Yarmouth, Shanklin, /.W.G.
Prothymnia viridaria.—C. on heaths ey.
Scoliopterya libatria.—C, ev.
LIST OF THE MACRO-LEPIDOPTERA. (28)
Plusia moneta.—Gen. dist. in gardens, larvae f. c.
Plusia chrysitis.—Gen dist., f. ¢.
Plusia chryson.—Between Winton and Kingsworthy, H.F.C.;
Monxton, 1 sp. 1908, H.; Has been taken in some plenty on Bramsbury
Common, H.
Plusia festucae—N.F., f. ¢., sometimes comes ‘to sugar, J.; Ring-
wood, N.; Soton, r. Johnson: Romsey, f. c., Pe., Dr. Buckell;
Winton, occ., Ht.; Shaw ford, Romsey, + Res Portsdown, Ilo, (Gay IBS 8
Fareham, 1 Sp., T.: L.W.., Freshw., Isp eae VE e229) eb radimes al
sp., Culver, 2 sp., L.W.G.
Plusia tota.—N.¥F., 0. c., B.j3 Ch. Fd., r., B.; Romsey, Pe.; Win-
ton, occ., R.; Portsdown, sc., Ps.; Alton, S.; Gen. dist. in Nth., H.,
Sl.; I.W., uncommon, /.W.G.
Plusia ppalielanaee—— NN Ringwood, N.; Damerham, 1 sp., Ct.;
Ch. Fd., A.; Alton, S.; Pamber, ¢c., Monxton, c., Longparish, H. ;
Sth. of Newbury, SL. ; LW. , old records only.
Plusia ni —Romsey, 2 sp. , Pe.
Plusia yamma,—Abt. ev.
Abrostola triplasia.—Romsey, Pe. ; Winton, se Jolin. 5 harobana: 1
Oa Ars LEUSVVUNELY TH, Cay 1B8 Cicia, dist. in Nth. H e SI. : Wes: old
records only.
Abrostola tripartita.—Ringwood, N.; Fdge., Ct.; Soton, r., F., A.;
Ch. Fd., sc., R., A.; Romsey, Pe. ; Winton, f. c., Ht.; Southsea, Hk. ;
Portsdown, n. c., B.; Gen. dist. in Nth., H., SI.; I.W., Shanklin,
Sandown, J.W.G.
Euclidia mi.—Gen. dist., c.
Euclidia ylyphica.—Gen. dist., c.; I.W., loc., Gurnard Bay only,
T.W.G.
Catephia alchymista.—I-W., M.B.I., 11. 78; Bembridge, 1 sp., 1858,
LW.G.
Catocala fraxtnt.—Alton, 1 sp., S.; 1.W., M.B.I., Il. 79; Occ.
single sp., 1.V.G.
Catocala nupta.—Gen., dist., ¢.
Catocala sponsa.—N.F., ¢., ". B.; Wurst Hill, ¢., M.; Ringwood,
Nes burley, bike Ren Ch “Vd Wes rab Wood, Ampfield, r., Ht. ;
Sheepwash, Horndean, nick B.; ca Sandown, J.W.G.
Catocala Pron en e CasSOMe my cS lunes. ae Hill, often
abt., M.; Ringwood, N.; Burley, Hk., R.: Ch. Fad., Re; Crab
Wood, Ampfield, r., Ht.: Sheepwash, n. c., B.; Harewood, Pamber,
c. some yrs., H.; I.W., Hampstead, r., 2. W ‘G
Toxocampa pastinum.—N.F., Ringwood, N.; Fdge., Ct ; Soton, loc.
f.c., F.; Winton, loc. c., Ht.; Fareham, 1 sp., H.; Swanwick, r., A. ;
Purbrook, n. c., T., B.; Sth. of Newbury, Sl.; I.W.; Freshw., c., Pe.,
T.; Ryde, n. c., B.; Yarmouth, Parkhurst, Haven Street, /.IV.G.
Laspeyria flenula—N.F., n.c., M., V.; Ringwood, N.; Soton, r.,
F’.; Ch. Fd., r., R.; Romsey, Pe.; Ptsmth., Ditcham, n.c., B.; Sheep-
De. Rs W ickham, 1 sp., T.; Abbotstone Down, 1 sp., S.; Sil-
chester, 1 Sp., H.; LW. 2 Sandown, Bembridge, 1. W.G.; Liphook, 1 sp.
Zaneloynatha Pistpennalie Neu): sce bee Chnistehyake = So0ton),
r., F.; Lordswood, n. ¢., M.; Ch. Fd., n.c., R.; Sheepwash, sc., Ps. ;
Alton, S.; c. in all woods in Nth., H.;: I.W., Sandown, Shanklin,
I.W.G. ;
Zancloynatha grisealts.—_N.¥., sc., B.; Ch. Fd.; n. c., R.; Soton,
fcaek. Te Wervohanklin= tc. WeGs
(24) THE ENTOMOLOGIST’S RECORD.
Zanclognatha emortualis.—Occurs, H.F.C.
Madopa salicalis—Ocecurs, H.F.C.; Petersfield, Barrett.
Herminia cribrumalis (cribralis)—Bogs ur. Ly., V.; M.B.J., I. 90;
Baddesley Common, f. c., F.
Pechipogon barbalis.—Gen. dist. in woods, c. _
Bomolocha fontis.—N.F., loc., B.; occ., M.; Soton, 1 sp., F.;
Wickham, 1 sp., T.; Woolmer, loc. c., E.; Pamber, c., Bere, c., H.
Hypena proboscidalis.—C. ev.
Hypena rostralis.—N.F., f. c., M.; n.c., V.; Soton, f. c., F.; Ch.
Bdiz nce Rc harchamyce Ia) Pismbihe mic. bss Havant. yer. Me:
Alton, oce., S.; Harewood, c., H.; Aldershot, c., Sn.; I.W., Brading,
Culver, Newport, /.1V.G.
Hypenodes taenialis (albistrigalis).—Ly., f. c., H.R., V. 227; Soton,
r., F.; Ch. Fd., n.c., R.; I.W., Sandown, H.F.C.; Parkhurst, Bem-
bridge, [.W.G.
Hypenodes costaestriyalis.—N.F., abt., V., a few, E.R., IX., 92.;
Soton, c., F.; Ch. Fd., f. c., R.; Alton, c., 8.; 1.W., Sandown, v. oce.,
Bembridge, /.1W.G.
Lhomoliges turfosalis.—N.F., c., H.R., 1X. 92, T.; Soton, abt., F.;
Shortheath, c., 8.
Brephos parthenias,—C. ev. among birch; I.W., East Cowes, J.1V.G.
Brephos notha.—Titchfield, Pamber, H.F.C.; I.W., East Cowes,
IW.G.
Pseudoterpna pruinata.—Gen. dist. on heaths and commons, more
or less c.
Geomctra papilionaria. —Gen. dist., not often c.
Geometra vernaria,— Gen. dist., c. on chalk.
Huchloris pustulata.—In all oak woods, usually se.
Nemoria viridata.—N.¥F., loc. ¢., A., T., M., Ht.; Ringwood, N. ;
Beaulieu, Brockt:: V:; Soton, loc. c., F.; Ch. Fd., c:., R.; Sth. of
Newbury, Sl.; I.W., Vent., /.W.G. | ;
Todis lactearia.—Gen. dist., c.
Hemithea strigata.—C. ev.
Hyria muricata.—N.F., .c., Ht.; loc. n. c¢., A.; Burley, f. c.,
R.; Ringwood, N.; Beaulieu, f. c., R., F.; Fdge., Ct.
Acidalia virgularia.—Gen. dist. in gardens, usually ec.
Acidalia straminata.—N.F., occ., M.; loc. ¢., T., A.;. Ly., V.;
Ringwood, N., H.F.C.; Beaulieu, r., F.,R.; Bomth., H.F.C.; Fdge., Ct.;
Headley Park, S.; Pamber, occ., H.
Acidalia interjectaria,—Bassett, A.; Ch. Fd., f. ¢., R.; Southsea,
Hk.; Ptsmth., r.. B.; Alton, 1 sp., 8.; I.W., loc., A.; Freshw., freely,
M.; Sandown, c., 1.W.G.
Acidalia humiliata.—I.W., Cliffs, B., T., ete., 1 sp., C.; Only
known British locality at Freshw., 1.W.G.
Acidalia holosericata,—Occurs, H.F.C.
Acidalia subsericeata.—N.F., Ringwood, N.; Ch. Fd., f. c., Ht.; St.
Catherine’s Hill, loc. c., F.; Portsdown, loc. c., Ps., T.; Pamber, c.,
H.; Sth. of Newbury, Sl.; I.W., n.c., A.; Nr. Sandown, Carisbrooke,
ILW.G.
Acidalia inornata.—N.¥., occ., M., A. ; Ringwood, N. ; Soton, r., F.;
Chiomds 1s c. Rs Horndean se. Bs yren mesh Alton) li spsoe:
I.W., Sandown, #.R., VILL. 174; Blackpan Common, 1 sp., /.W.G.
Acidalia aversata.—C. ev., var. spoliata occurs freely.
LIST OF THE MACRO-LEPIDOPTERA. (25)
Acidalia degeneraria.—I.W., Sandown, 1 sp., #.R., XLV. 274.
Acidalia bisetata.—Gen. dist., c.
Acidalia dimidiata.—N.F., Hk.; Ringwood, N.; Soton, f.c¢., F.,
AG Che Ndi: ce, ke Ae Winton ee: Hits; Portsdown, Purbrook,’¢
Ps., B.; Havant, c., H.; Alton, S.; Sth. of Newbury, Sl.; I.W.,
Sandown, c., J. WV.G.
Acidalia trigeminata.—Gen. dist., n. c.; I.W., old records only.
Acidalia ornata.—Chalk districts, f. c.; I.W., f. ¢., V.
Acidalia remutaria.—e. ev. in woods; I.W., Sandown, J.W.G.
Actdalia tmmutata.—N.F., loc., A.; Ringwood, N.; Baddesley, c.,
I’.; Winton, IV.L. 1891; Alton, Kingsley, c., 1920, 8.; I-W.,
between Sandown and Shanklin, 1 sp., 1.V.G.
Acidalia marginepunctata.—N.F., Ringwood, N.; Sway, Ct. ; Soton,
n.c¢., A.; Romsey, Pe.; Winton, W./.., 1891 ; Portsdown, Hayling,c
Psa;) Havant, io; Wareham, no. c!, 05; 1Ws A, V., Han.; TLE 204 ;
St. Lawrence, f. c., B.; Shanklin, Sandown, Niton, Yarmouth, Vent.,
c:, L.IV.G.
Acidalia enutaria.—N.¥., c., J., T., B.; Ringwood, N.; Bogs, Ly.,
Brockt., V.; Romsey, Pe.; Cosham, c., T., Ps.; Gt. Salterns, sc.,
Ealing Wc. oRs Wea eee tect) iin ahs Ile) Varmoutis Ve. Acs
Freshw., c., M.; St. Helens, 7.W.G.
_ Acidalia imitaria.—N.F., Ringwood, N.; Fdge., Ct.; Soton, n. c.,
iB} peeenss Clie oides nt cs ha tA sehomseys meas Winton, t- Caribe:
Portsdown, f. c., Ps., %.; Havant, f.-c:, E.; Alton, 1 sp., S.; Gen.
dist. in Nth., H., Sl.; I.W., Sandown, f. c., /.1V.G.
Acidalia ochr ite Ee ecombe: 1 sp. by Rew E. H. Todd, 1900, R. ;
MWe AWB NUkas BRAS 12 a Nails 341.
Ania emaryinata.—N.F., Pe., H.HR., 1X. 1892; Ringwood, N.; Ch.
Id., i. c¢., R., A.; Romsey, Pe.; Crab Wood, W.L., 1875; Ptsmth.,
Gt. Salterns, f. c., Ps., B.; Headley Park, S.; Pamber, c., H.; Sth. of
Newbury, SI.; I. W., Sandown, r., Horringford, 1 sp., /.W.G.
Timandra ucees —Gen. dist., usually c.
Ephyra porata..—N.F., n. c., B.; Ringwood, N.; Fdge., f. ¢., Ct. ;
Bassett, A.; Soton, sc., F.; Ch. Fd., f. ¢., R.; Romsey, Pe.; Crab
Wood, n. c., Ht.; Rowlands Castle, sc., Ps.; Gen. dist. in Nth., H.,
SI. ; I.W., Sandown, oce., Bembridge, 7.W.G.
aS punctaria.—N.F., f. c., M.; Ringwood, N.; Sway, Ct.;
Dolton aiaiceek. As > Wastleii~ mech Chev Hd: fic. 7, vAe;
Romsey, Pe. ; Cra Wwieod: Ampfield, f.c., Ht.; Fareham, Harewood,
c., Pamber, oles Wood, Hyden Wood, H Sth. of Newbury, SI. ;
LW., Centurion’s Copse, Saude. T:W:G.
Ephyra linearia.—N.F., c., M., T., F., ete. ; Fdge., Ct. ; Ch. Fd.,sc.,
R., K.; Romsey, Pe.; Winton, c., Ht.; Rowland’s Castle, Hyden
Wood, Finchdean, c., Ps:, B.; Selborne, c., S.; Doles Wood, H.; Sth.
of Newbury, les Te W., Calbourne, I.W.G.
Ephyra annulata. —c. ev. where maple abounds.
Ephyra orbicularia.—N.F., f. c., M., A.; Ly., f.c., Ht.; Soton, r.,
F.; Crab Wood, ocec., Ht.; I.W., old records only-
Ephyra pendularia.—N.F.,c., M., Ht., A.; Ringwood, N.; Soton,
e., F., M., A.; Ch. Fd., n.c:., R., K.; Romsey; Pe; Winton, W.L.,
1891 ; Westbourne, Gon Hyden "Wood, sc., Ps.,.B.; Fareham, H.;
Pamber, Vics Harewood, H:
Sterrha sacraria.—Oce. immigrant sp. on ie coast ; No very recent
record.
’
(26) |THE ENTOMOLOGIST’S RECORD,
Ortholitha plumbaria.—e. nearly ev. among gorse and broom.
Ortholitha cervinata. —N.F., Ringwood, N.; Fdge., Ct.; Ch. Fd.,
c., A.; n. c., R.; Romsey, Pe.; Portsdown, Bedhampton, e., Ps.;
Fareham, n. c., T.:; Alton, f. c., S.; Andover, c., Pamber, H.; Sth. of
Newbury, SI.; J. W., Sandown, Cowes, Shanklin, /.W.G.
Ortholitha linitata.— ¢. nearly ev. .
Ortholitha bipunctaria.—e. ev. on chalk. 5
Mesotype virgata.—N.F., Ringwood, N.; Shawford, n. c. R.;
Romsey, Pe.; Winton, log. c,, F., M., T.; St. Catherine’s, Twyford
Downs, loc. c., Ht.; Hayling, c., Ps.; 1.W., St. Lawrence, n. c., B. ;
Freshw., A.; Bembridge, Freshw., /.W.G.
Minoa murinata.—N.F., n. c., M.; Ringwood, N.; Brockt.,
Rhamnor, R.; Edge., Ct.; Bassett, n. c...A.; Winton, f. c., Ht. ;
Fareham, n.c., T.; Rowlands Castle, f.c., Ps., B.; Alice Holt,r., S. ;
Pamber, c., T., H.; Doles Wood, H.; Nr. Basingstoke, A.; I.W., old
records only.
Odezia atrata.—N.F., loc., sometimes abt., M., T., Ht., A.; Ring-
wood, N.; Brockt., Ct. ; Ampfield, occ., W.L., 1891; 1.W., Parkhurst,
DAWG
Anaitis plagiata.—Gen. dist., usually c.
Chesias spartiata. N.I., Ringwood, N.; Soton, c., F., A.; Tast-
leigh, c., K.; Ch. Fd., f. c., R., A.; Romsey, Pe.; Sheepwash, Horn-
dean, c., Ps., B.; Tadley, f. c., H.; I.W., Shanklin, Cowes, /.W.G. —
Chesias rufata.—Soton, 1 sp., M., f. ¢. but very local, F.; Sheep-
wash, 2 sp., B.; Oakhanger, 8S.
Lobophora polycommata.—Occurs, V., M.B.1., Il. 152; Ringwood,
N.; Little Park, Hk.
Lobophora carpinata.—N.F., f. c., A., M., B.; Ringwood, N.; Soton,
fesC;, tien Ay Ch. Wd fcr, Rey A. Crab. Wood, 2.) EW.
Parkhurst, Cowes, Shanklin, /.1W.G.
Cidaria siderata.—N. F., c., T., M., Ht.; Ringwood, N.; Ch. Fd.,
r., R.; Romsey, Pe.; Havant, H.; Pamber, Longparish, H.; Sth. of
Newbury, Sl.; I.W., old records only.
Cidaria..niata:—N.F., occ. M.; Ringwood, N.; Soton, r., F.;
Kastleigh, oce., K. ; ; Romsey, Pe. ; Hursley, r. , R.; Winton, oce., Ht. ;
Fareham, sc., Ps.; orersheld: (5 Pa: Alton, if C., 'S.: dover Pam
ber, H.; Sth. of Newbury, S1.; iL Ww, old-records only.
Thera variata.—N.F., v. Ieee AS Weoodtorde - Wootton, 1915, Ct.;
Ch. Fd., loc. c. among spruce, R.; Soton, loc.c., I*.; Tisted, Headley
Park, S.; See Hnt., XLV. 241.
lies obeliscata. gt ey. among pines.
_ Thera cognata (simuleta).—- Occurs, ¥.
-. Thera firmata.—f. c. ev. among Scots’ pine; I.W., old records only.
Thera juniperata.—Occurs, V.; Dean Downs, Pe.; Abbotstone
Down, abt., S. ~
Lampropterya suffumata.—N.F., Brockt., R.; Denny, F.; Ch. Fd.,
sc., R.; Fareham, n.c., T.; Hayling, n.c., B., K.; Alton, 8S. ; Harewood,
Bere, H.; Sth. of Newbury, Sl.
(28) THE ENTOMOLOGIST’S RECORD.
Coremia quadrifasciaria.—Occurs, Ht.; M.L./., Il. 180; Sth. of
Newbury, Si.; I.W., Landslip, /.1V.N.H.S.
Coremia unidentaria.—e. ev.
Coremia ferrugata.—c. ev.
Coremia designata. —Gen. dist., usually c.; I.W., Shanklin, San-
down, /.W.G.
Amoebe olivata.—I.W., St. Lawrence, f. c., B.; Pelham Woods,
Vent., 1 sp., J.W.G.
Amoebe viridaria.—e. ey., often abt.
Malenydris multistrigaria.—N.F., ¢., B.; Ringwood, N.; Soton,
abt., F.; Bassett, A.; Hythe, T.; Ch. Fd., n.c., R., A.; Winton, c.,
Ht.; Horndean, n. c, Ps., B.; Harewood, Pamber, H.; Sth. of
Newbury, Sl.; I.W., Sandown, 1 sp., [.W.G.
Malenydris didymata.—e. ev.
Oporabia dilutata.—Gen. dist. in woods, c.
Xanthorhoé montanata.—-Abt. ev., F.
Xanthorhoé fluctuata.—Abt. ev., F.
Xanthorhoé galiata.—Winton, f. c., Ht.; Portsdown, Hayling, c.,
Ps., T., B.; Sth. of Newbury, Sl.; I.W., Sandown, c., Vent., 1.W.G.;
Freshw., Pe.
Xanthorhoé rivata.—N.}"., Ringwood, N.; Soton district, gen. c.,
M.; Romsey, Pe.; Winton, c., Ht.; Portsdown, c., Ps., B.; Long-
parish, c., H.; Sth. of Newbury, Sl.; I.W., A.; Sandown, Freshw.,
Luccombe, J.W.G.
Xanthorhoé sociata,—Abt. ev.
Xanthorhoé tristata.—Sway, Ct.; Bassett, c., M.; Hastleigh, f.c., K.
Xanthorhoé unangulata.—N.F., Ly., n. c., Ht.; Ringwood, N.;
Bnmth., n. c., M.; Christch., Dt.; Ch. Fd.,n.c., R., A. ; Romsey, Pe. ;
Silkstead, W.L., 1875; Purbrook, se., Ps., B.; Alton, n. c., S.; Nth.
of Basingstoke, Tadley, Silchester, Pamber, etc., H.; Sth.of Newbury,
Sl.; I.W., Sandown, loc. c., 1.W.G.
Huphyia picata.—N.F., Ringwood, N.; Christch., Dt., R.; Ch. Fd.,
r., R.; Horndean, 1 sp., B.; Nth. of Basingstoke, f. c., H. ; Sth. of
Newbury, Sl.; I.W., Sandown, Shanklin, Brading, /.W.G.
Eulype hastata.—Formerly v. r. in Hants, according to old records ;
N.F., Ringwood, N.; Soton, c., F., A.; Hursley, Lordswood, f. c., M. ;
Kastleigh, c., K.; Ch. Fd., f. c., R., A.; Dean Downs, Pe.; Winton,
f. c., Ht.; Hyden Wood, Westbourne, B., Ps. ; Fareham, c., T.; Alton,
loc. c., 5.; Harewood, v. c., Pamber, c., H.; Andover, SI.
Mesoleuca albicillata.—Gen. dist. in woods, n.c.; I.W., Sandown,
L.W.G.
Mesoleuca bicolorata.—N.F., Ringwood, N.; Fdge., f.c., Ct.; Soton
district, n.c., M., A., F., K.; Romsey, Pe.; Ampfield, 1 sp., Ht.;
Portsdown, n. c., B.; Havant, f. c., E.; Alton, r., S.; Pamber,
Monxton, occ., H.; I.W., Sandown, Brading, /.V.G.
Melanthia procellata.—e. ev. among clematis.
Perizoma affinitata—N.F., Ringwood, N.; Christch., Dt.; Ch. Fd.,
sc., R., A.; Chalton Downs, f. ¢., Ps.,.B.; Alton, S.; LW.,c¢., 1.W.G.
Perizoma alchemillata.—N.F., Ringwood, N.; Christch., r., R., Dt.;
Holmsley, R.; Baddesley, r., F., Shawford, f.c., R.; Ch. Fd., n. c¢.,
A., R.; Chalton Down, 1 sp., B.; Little Park, Hk.; Pamber, H. ;
Sth. of Newbury, Sl. ; I.W., Sandown, larvae sometimes abt., J.W.G.
Perizoma flavofasciata (decolorata).—N.F., Ringwood, N., Christch.,
LIST OF THE MACRO-LEPIDOPTERA. (29)
Dt.; Soton, loc. c., F.; Ch. Fd., loc. c., R., A.; Winton, r., Sweeting ;
Havant, K.; Alton, 8.; Harewood, H.; I.W., Shanklin, Sandown,
I.W.G.
Perizoma albulata.—N.F., Ringwood, N.; Soton, Eastleigh, loc. c.,
Bea Ch. ides feet iss Winton, fc..iates: - Ovington, S.; Woolmer, loe.
Ce E.: Sth. of Newbury, SI. ; L.W., Ce Shanklin Down, Bonchurch,
ILW.G
Perizoma bifasciata.—N.F., n. c., M.; Ch. Fd., sc., R.; Winton,
1 doubtful sp., V.L., 1875; Hayling, Dr. Hay; I.W., Sandown, larvae
usually abt., 7.W.G.
Perizoma taeniata.—Portchester, [nt., 1912, p. 82.:
Camptogramma bilineata.—Abt. ev.
Hydriomena furcata (sordidata).—c. ev, among sallows; I.W.,
Shanklin, Cowes, Sandown, J.W.G.
Hydriomena impluviata (trifasciata)—N.F., c., M., Ht., A.; Fdge.,
fice Cie. Soto, ft. c¢.. Ae Kev ChaiWd:. fey Ray Rambersc. cla.
I.W., Sandown, J.W.G.
Hydriomena ruberata.—N.F., r., B.; Ringwood, N.; Bassett, r., A.;
Soton, r., F.; Purbrook, Southwick, sc., Ps., B.
Anticlea cucullata.—Wootton, 1 sp., R.; Romsey, 1 sp., Pe. ;
Winton, v. r., W.L., 1891; Emsworth, Mr. Christy takes it, H.
Anticlea badiata.—c. nearly ev.
Anticlea berberata.—Romsey, Pe.; Winton, not uncommon in our
lanes, Hits, Wer. 1891.
Anticlea rubidata.—Gen. dist., V.; N.F., Ringwood, N.; Sway, Ct.;
SOUOMy Tals Co, Hee Clone IN ies eae 3 - Romsey, Pe. ; ; Winton, ¢c., Ht. ; Port-
chester, n. G., T.: Portsdown, Sheepwash, Oey Leh BBS " Andover, HE:
TEWesesil- W.G.
Destin nigrofasciaria. Gan dist., rarely c.; I.W., Brading, 1 sp.,
I.W.G.
Euchoeca obliterata —N.F., n. c., M., Ht., N., etc.; Soton, ¢c., F.;
Ch. Fd., n. c., R.; Fareham, n. c., T.; Sheepwash, sc., Ps.; Headley
Park, S.; Pamber, v. c., H.; Sth. of Newbury, Sl.
Asthena candidata.—Gen. dist., ¢.
Asthena luteata.—Gen. dist. among maple, sometimes c.; Soton, c.
among alder, F.
Asthene testaceata (sylvata).—Crab Wood, W.L., 1875; Occurs, V.;
Portchester, Hnt., 1912, p. 32.
Eupithecia ollonmeatin. —c. ey., especially in gardens.
Eupithecia pulchellata. _N.E,, 6c, TS ial, 2 SOOM, tte Cay Hg ks 8 (Ohta
Fd., v.c., R.; Sheepwash, Rowlands Castle, ete., f.c., Ps., B.; Havant,
C., E..: I. vie, ‘Bord wood, St. Boniface Down, Sihouleien. I, W.N.A.S.
E uopiiiheede linariata.—c., V.; Ch. Fd., n. c., R., A.; Bursledon, A. ;
Winton, c., F.; Silkstead, W.L., 1875; Clanfield, f. c., Ps.; Horndean,
Nec sab:
Eupithecia irriqguata,—N.F., loc. n. c., M., A.; Brockt., Rhamnor,
oce., R.; Denny, Holmsley, F.; NE. only, V.; Crab W ood, Ht.
Beystihor a pusillata.—N.F., e D.;. ELt.; Broekt., 5 8 lng 186k,
c. some yrs., R.; Westbourne, c., Ps.; Havant, £, ¢., B: ; Tisted, c., S.;
1.W., old records only.
KE upithecia indiyata,—Occurs, V.; Ch. Fd.,n.c., R., A. ; Sarisbury,
1 sp., T.; I.W., old records only.
iSarntlbenic insigniata (consiynata).—Hayling, M.B.I., 11. 227.
(30) THE ENTOMOLOGIST’S RECORD.
Hupithecia venosata.—N.F., sc., B.; Soton, f.c., F.; Ch. Fd., f.°c.,
R., A.; Winton, c., Ht., K., F.; Fareham, c., T.; Portsdown, Broad-
halfpenny Down, c., Ps., B.; Sth. of Newbury, Sl.; I.W., Sandown,
etc., 1.W.G.
Eupithecia pimpinellata.—Occurs, V.; St. Catherine’s Down, r., R.;
Shawford, r.. R.; Farley Mt., W.L., 1875; I.W., Culver, Brading
Down, elie, LW. @.
iBanvdabeata ewpallidata. —Westbourne, R.; Ch. Fd.,¢., R., A. ; 1.W.,
old and doubtful records only.
Hupithecia assimilata.—Occurs, V.; Boscombe, R.; Soton, sc., F.;
Ch. Fd., n. c., R:, A.; I.W., Sandown, ¢c., Yarmouth, /.W.G.
Hupithecta absinthiata.—N.F., c., B.; Wootton, Ct. ; Christch., Dt. ;
Soton, c., M., F., A.; Ch. Fd., Farley Mt. c., R., A.; Winton, f. c.,
Ht.; Fareham, c., 2. ; Southsea, Hk.» -Pismth foc.) Ba awe,
Sandown, c., Yarmouth, J. W.G
Hupithecia goossensiata (minutata).—N.F., f. ¢., B., Ht.; Ch. Fd.,
se., R., A.; Hyden Wood, n. c., B.; I.W., old and doubtful records
only.
Hupithecia denotata (campaniulata).—Portsdown, 1 sp., Ps.; Alton,
one locality, c., S.; I.W., loc. (Meyrick’s Handbook), 7.1V.G.
KMupithecia albipunctata.—Bassett, c., M., A.! Soton, F.; Ch. Fd.,
co Ra Aes Winton! t..c. Wel, 189i =- Westbourne: ee Ose
IB ERL 2 Alton! San Wie igandonnt loc., Shanklin J.W.G
Bratanars spills ne ev.
Fupithecia trisignaria.—Ch. Fd., r., A.; I.W., Swainston, Row-
ridge, 7.W.N.H.S.
Hupithecia lariciata.—Abt., V.; Holmsley, R.; Bnmth., n.c., M. ;
Boscombe, r., R.; Soton, f. c., F.; Ch. Fd., r., R.; Crab Wood,
f.c., W.L., 1891; Westbourne, sc., Ps., B.; Horndean, c., Ps.; Little
Park, Hk.
Hupithecia eastigata.—Kdge., Ct.; Boscombe, R., Dt.; Soton, f. ¢.,
F.; Ch. Fd., f. ¢., R., A.; Winton, f.c., Ht.; n.c., M.; Hyden Wood,
f. c., Ps.,B.; Sth. of Newbury, SI.; I.W., Sandown, Yarmouth, = W.G.
Hupithecta subnotata.—Boscombe, R.; Soton, A.; Ch. Fd., se., B.,
A.; Winton, W.L., 1875; Portsdown, Hayling, Gt. sateen Pees
IPs, 16% 8 dls Wa, Sandown, c., Shanklin, /.WV.G.
Bupithecia satyrata, — Farley Mt., Hursley, fe Cs R.; Winton, sc.,
F., A. ; Portsdown, sc., Ps., B.
Hupithecia succenturiata.—Bumth., se., R., Dt.; Ch., Fd., se., B.,
A.; Ditcham, r., B.; Sth. of Newbury, Sl.; I.W., Sandown, loc.,
Bordwood, J.1V.G.
Huptithecia subfulvata.—Christch., Dt.; Bassett, A.; Ch. Fd., se.,
R., A.; Hursley, c., M.; Winton, occ., Ht.; Fareham, c., T.; Ports-
down, Hayling, Horndean, f. c., Ps.; Havant, c., E.; Sth. of Newbury,
Sl]; I.W., Sandown, Shanklin, 1.W.G.
Hupithecia scabiosata.—Soton, r., F.; Shawford, Hursley, r., RB. ;
Winton, A.; St. Catherine’s Down, c., F.
Hupithecia haworthiata (isogrammaria).—Shawford, f. c., R.; Win-
ton, c., M., Ht.; Fareham, c., T.; Portsdown, abt., B., Ps.; Alton, c.,
See W., A,; Sandown, Brading, I.W.G.
apeiecns ellenticeranig. NN, f. c., Ht.; Boscombe, R.
Hupithecita plumbeolata.—Ch. Fd., c. some yrs., R., A.; Aldershot,
1 sp., Sn.; Basingstoke, A.; I.W., Bordwood, I.W.G.
LIST OF THE MACRO-LEPIDOPTERA. (31)
Eupithecia tenwiata.—N.F., n. c., B.; Ch. Fd., f. ¢., R.
EFupithecia inturbata (subciliata).—Alton, larvae abt., 1920, 8.
Eupithecia innotata.—I.W., Sandown, 1 bred, #/.R., 1904, p. 336.
EKupithecia fraxinata.—Occurs, V., Ht.; Winton, r., F.
Hupithecia nanata.—c. ev. on heather, F.
Eupithecia abbreviata.—N.F., c., T., M., Ht.; Soton, c., F., A.; Ch.
Fd., f. c., R.; Crab Wood, W.L., 1875; Horndean, Rowlands Castle,
Sheepwash, Catisfield, etc., c., Ps., B.; Sth. of Newbury, Sl.; I.W.,
Sandown, /.W.G.
Hupithecia dodoneata.—N.¥., n.c., M., B., A.; loc., Ht.; Brockt.,
he Dennvceste bomthie is. Dt. Ovum, Me. tis ©hwhideens ace.
R., A.; Crab Wood, Ht.; Wickham, sc., Rowlands Castle, f. c., Ps., B. ;
I.W., Cowes, Shanklin, 1.W.G.
Eupitheeia exiguata.—Bassett, A.; Ch. Fd., sc., R.; Crab Wood,
oce., Ht.; I.W., Sandown, [.W.G.
EHupithecta sobrinata.—Farley, f. c., R.; Winton, A.; Chalton,.
Finchdean, abt., Ps., B.; Abbotstone Down, 8.; I.W., Shanklin,
several, 1.W.N.H.S.
Gymmnoscelis pumilata.—N.F., c., T., M.; Beaulieu, ¢., F.; Soton,
c., F.; Ch. Fd.,c., R.; Winton, n. c., Ht.; Southsea, Hk.; Ports-
down, Westbourne, etc., abt., Ps., B.; Headley Park, c., 8.; IW.,
Sandown, Shanklin, J.1V.G.
Hucymatoye togata.—N.F., f.c., Ht., M.B.1., Il. 251; Ly., H.R.,
IX. 211.
Chloroclystis coronata.—N.F., c., M.; Soton, sc., F.; Ch. Fd., n.c.,
R., A.; Winton, f. c., Ht.; Portsdown, Finchdean, c., Ps., B.; Alton,
f.c., S.; Sth. of Newbury, Sl.; I.W., Sandown, I.W.G.
Chloroclystis rectangulata.—N.F., n. c., M.; Fdge., n. c., Ct.; Soton,.
fs Wy Ans, Oh Hd fic). A.) Wintont cs Eth: Btsmths lave
ling, f.c., Ps. B.; Havant, H.; Alton, 8.; Sth. of Newbury, Sl. ;
I.W., Shanklin, J.W.N.A.S.
Collia sparsata. —N. EK, MBL, WW. 2645 lay... Il: 183 7Ch:
Fd., f. c., R. ; Romsey, Pe.; Pamber, H.
Pelurga comitata.—Occurs, V,; Bumith., 1 sp., 1920, S.; Romsey,
Pe. ; I.W., Sandown, c., Shanklin, I.W.G.
Phibalapteryx vitalbata.—c. ev. among clematis, F.
Phibalapteryx tersata.—c. ev. among clematis, F.
Ooenocalpe vittata.—N.F., Ringwood, c., T., N.; Brockt., Hk. ;
Christch., S., Dt.; Soton, 1 sp., F.; Ch. Fd., sc., R.; Romsey, Pe. ;
Winton, water meadows, n. c., W.L., 1891; Cosham, f. c.,
Purbrook, sc., Ps. B.; Woolmer, c., E.; Shortheath swamp, S. ;.
Andover, Thruxton, V.; I.W., Freshw., Bembridge, Brading, /.W.G.
Percnoptilota fluviata. —N.F., Ringwood, N.; Brockt., 1899, Ct. ;
lives losp., Ve Christch., Dt. Soto, sp. Che ihid ai spi. An:
Cosham, 1 sp., T.; I.W., Sandown, 1 sp., Shanklin, 4 sp., other older
records also, 1.W.G.; Freshw., Pe.
Abraxas sylvata.—Winton, 1 sp., 1890, W.L., 1891; Hambledon,
H.F.C.; Alton, loc., S.; I.W., Vent., C.; Pelham Woods, f. ¢., Park-
hurst, 1.W.G.
Abraxas grossulartata.—e. ev.
Lomasptlis maryinata.—Gen, dist., ¢c.
Ligdia adustata. —c. ev. among spindle, F.
(32) THE ENTOMOLOGIST’S RECORD.
Aleucis pictaria.—N.F., c., M., T., Ht.; Ringwood, N.; Bassett, r.,
A.; Winton, Ht.; Finchdean, f.c., Ps., B.
Bapta bimaculata.—Gen. dist., loc., usually c.; I.W., rare, Bord-
wood, 1 sp., [.W.G.
Bapta temerata.—Gen. dist., f. c.; I.W., Shanklin, loc. ¢., 1.1V.G.
Cabera pusaria.—Abt. ev.
Cabera exanthemata.—e. ev.; I.W., Sandown, ¢., 1. W.G.
Numeria pulveraria.—Well dist. but somewhat se. |
Ellopia prosapiaria.—Gen. dist. among fir, usually c.
Metrocampa margaritaria.—f. e. in all woods, F.
Itnnomos autwmnnaria,— Ch. Fd., r., R.; Fareham, f. c., T., H.;
Southsea, Hk.; Ptsmth., both sexes f.c. at light, Ps. B.; Hayling,
Dr. Hay.
Ennomos quercinaria.—N.F., c., F., M., Hk.; Soton, n. c., F.;
Eastleigh, f. c., K.; Ch. Fd., sc., R.; Winton, c., Ht.; Southwick, f.c.,
Ps., B.; Alton, S.; Andover, H.; Sth. of Newbury, Sl.; I,W.,
Shanklin, Sandown, Cowes, n. ¢c., I. WV.G.
Ennomos alniaria.—N.F., f. c., M.; Ringwood, N.; Bumth.,c., Ct.,
Hikys-Sotons fc.) Hig sn Ae iOhtid tach ohe ale > 7 Hastlelehns mance
K.; Remsey, Pe.; Winton, f.c., Ht.; Bedhampton, Emsworth, sc.,
Ps., B.; Alton, n. c., S.; Andover, c., H.; I.W., f. c., Shanklin, San-
down, Cowes, /.W.G.
Ennomos fuscantaria.—N.F., Ringwood, N.; Soton, c., F., V.;
Eastleigh, n. c., K.; Winton, Ht.; Southwick, Ptsmth., se., Ps., B.;
Fareham, n. c., T.; Andover, H.; I.W., Cowes, Shanklin, J.W.G.
Ennomos erosavia.—N.F¥., f. c., M., B.; v. r., T.; Ringwood, N.;
Soton, sc., F., A.; Ch. Fd., sc., R., A.; Kastleigh, occ., K.; Romsey,
Pe.; Winton, Ht.; Ptsmth., n.c., B.; Horndean, 1 sp., Ps.; Hare-
wood, H.; I.W., old records only.
Selenia bilunaria.—Gen. dist., c.; var. juliavia N.F., M.
Selenia lunaria.—Brockt., 1 sp., T.; Soton, 1 sp., F.; Sth. of New-
bury, Sl.
Selenia tetralunaria.—N.F., n.c., M., A.; ¢., Ht.; Ringwood, N.;
Soton, r., F., A.; Ch. Fd., se., R.; Eastleigh, n.¢., K.; Romsey, Pe.;
Crab Wood, 1 sp., Ht.; Westbourne, f.c., B., Ps.; Hampage Wood,
1sp,5.; Pamber, 2 sp., H.; Sth. of Newbury, SI.
Hyyrochroa syringaria.—N.F., f. c., M., F.; Ringwood, N.; Hordle,
Ct.; Soton, c., F., K.; Ch. Fd., f. c., R.; Romsey, Pe.; Ampfield, n.c.,
Ht.; Westbourne, sc. B., Ps.; Alice Holt, 1 sp.,S.; Gen. dist. in Nth.,
H., Sl. ; I.W., Newport, Sandown, Cowes, n. c., 1.W.G.
Gonodontis bidentata.—Gen. dist. but n. c.; I.W., ¢., 1.W.G.
Himera pennaria.—Gen. c. in woods, F’.
Crocallis elinguaria.—Gen. dist., usually ec.
Angerona prunaria.—Many localities, especially N.F., V.; N.F., r.,
Aves Chethde az. 0X @rabeWood et.csicligen Harahan m7 es eluuelins
Southwick, se., Purbrook, f. c., Ps., B.; Havant, n. c., K.; Hayling,
1 sp., Dr. Hay; Selborne, Alice Holt, 8.; Pamber, c., H.; IW.,
Bembridge, Freshw., [.W.G.
Ourapteryx sambucaria.—e. ev.; an occ. second brood occurs, F.
Hurymene dolabraria.—N.F., oce., M., B.; Ringwood, N.; Fdge.,
se Cas Sotons sche.) Bassett-maics vACewaCla iG iaiee (Ch kues Ace
Hursley, occ., M.; Crab Wood, n. ¢., Ht.; Fareham, oce., T., H. ;
Horndean, Rowlands Castle, sc., B., Ps.; Alton, §.; Harewood,
LIST OF THE MACRO-LEPIDOPTERA. (383)
Pamber, Doles Wood, H.; Andover, Sl.; I.W., Ninham, Sandown,
Cowes, J.W.G.
Opisthograptis luteolata.—abt. ev.
Epione apiciaria.—N.F., sc., B.; Ringwood, N.; Soton, sc. and
loc., F.; Bassett, f. c., A.; Ch. Fd., n.c., R., A.; Hastleigh, n. c., K.;
Romsey, Pe. ; Winton, 1 sp., Sweeting; Fareham, n.c., T.; Ptsmth.
district, loc., n. ¢., Ps., B.; Pamber, c., Monxton, H.; Sth. of New-
bury, SI. ; LW., “Caan. Ent., 1889, p. 236; Sandown, Shanklin,
Niton, J. WV. G.
Epione parallellaria.—Occurs, H.F.C.; one or 2 sp. nr, Kmery
Down, V.
Hpione advenaria.—Loc. abt. in woods throughout; N.F., n.¢., A.;
Chashidantceshys he sACt al a Wkeebanicnurs table spt le aaGr
Venilia maculata.—A bt. in all woods.
Semiothisa notata.—Occurs, V.; N.F., Ringwood, N.; Bnmth., se
Ct.; Fareham, 2 sp., H.; I.W., Sandown, 1.W.G..
Semiothisa alternata.—N.F., f. c., M.; ¢., H.; n.c., T.; Ringwood,
N.; Bnmth., Damerham, 1 sp., Ct.; Soton, loc..c., F., A.; Ch. Fad.,
@., R., A.; Romsey, Pe.; Wickham, n.c., T.; Havant, r., B.; 1.W.,
M.B.1., I. 288; old records only for I1.W.
Semiothisa litumata.—More or less c. ev. among Scots pine.
Hybernia rupicapraria.—e. ey.
Hybernia leucophaearia.—e. in all woods, sometimes abt., very
variable.
Hybernia anvantiaria.—e. ev. in woods, and at light; IW, old
records only.
Hybernia marginarta. — G. ev.
Aybernia defoliaria.—e. ev. in woods nad gardens; very variable.
Anisopteryx aescularia.—Gen. dist., more or less c.; Soton district,
Shee a TAs
Phigalia pedaria.—Gen. dist., usually ce.
Apocheima hispidaria.—Most uncertain in appearance and vy. loc. ;
N.F., occ., M., Ht.; Ringwood, N.; Ch. Fd., sc., occ. abt., R.; Soton,
usually r., sometimes c., F., K.; Rowlands Castle, Horndean, occ., ¢.,
Ish, 1B. 2 Islenaaly Gos Ie Peranlosye. Gay Jals
Lycia hirtaria. —N.F., Ringwood, N.; 5 Canam. , Dt.; Bassett, 1 sp.,
A.; Finchdean, Soachmicle S@umesas Slava Gon 155 5 Pamiber! Ibo been
Pikent Jale
Pachys strataria.—Gen. dist. in woods, rarely c.; males f. c. ev. at
light.
2 Pachys betularia.—Gen. dist., c.; ab. doubledayaria about 20% and
increasing ; intermediate forms v. r.
Hemerophila abruptaria.—Gen. dist., somewhat sec.; I.W., c.,
PWG.
«° Boarmia cinctaria.—N.F., loc. c., T., B., M., ete. ; Ringwood, N. ;
Brockt., ¢., R., ete: ;-Ly., V., etc. ; Ampfield, oce., Ht. ; Pamber, Alton,
Sits he:, baa
Boarmia yemmarta.—e, ev. : Bat
Boar:nia abietaria.—N.F., loc. c., M., Ht., etce.; Eastleigh, f. c.,
K.; Chalton Downs, Finchdean, abt., Ps., B.; Rowlands Castle, Hk. ;
Woolmer, c., E. ;. I.W., old-records only.
. Boarmia repandata.—Gen. oe c.; ab. conversaria f. c.
Boarmia roboravia.—N.F., c., T., M., A.; Burley, Hk. ; ee
(384) THE ENTOMOLOGIST’S RECORD.
N.; Soton, c., M., F., K.; Ch. Fd., f. ¢., R., A.; Crab Wood, Ampfield,
f. c., Ht.; Horndean, Rowlands Castle, f. c., Ps., B.; Woolmer, c., E.;
Pamber, C., H.; LW., Cowes, I.W.G.
Bot. mae naaoni ana LN F., c., T., B.; Ringwood, N.; Soton
district, c., F., K., M.; Ch. Fd., f. ¢., R., A-; Winton, Ht. ; South:
wick, Westbourne, c., Ps., B.; Alice Holt, c., S.; Pamber, ¢c., H.;
I.W., Cowes, I.W.G.
Mleora angularia,—N.F., v. r., V., H.F.C.; Not seen since 1872, so
far as can be ascertained.
Cleora lichenaria.—Gen. dist. in all larger woods, but rarely ec. ;
Jhon Og Jl WG
Cleora jubata (ylabrarvia).—N.F., f. c., T., M., Ht., ete. ; Ringwood,
N.; Holmsley, f. c., R.; Denny, r., Soton, loc., f.c., F.; Ch. Fd, se
R., A.; Woolmer, f. c., E.
Tephrosia bistortata.— e. ev. in woods. Double brooded.
Tephrosia crepuscularia,—e. ev. in woods; rare in I.W.
Tephrosia luridata.—N.F., f. c., M., B.; Ringwood, N.; Soton, f. c.,
F.; Ch. Fd., se., R., f. ¢:, A.; Winton, r., Ht.; Rowlands Castle,
Horndean, Sheepwash, n.c., B., Ps.; Shansted, Hk.; Harewood,
Pamber, H.; I.W., nr. Shanklin, Parkhurst, /.1V.N.A.S.
Tephrosia consonaria.—Loe. ¢. in nearly all larger woods, irregular
in appearance ; I.W., Cowes, loc., Freshw., J. W.G.
Tephrosia punctularta.—Loce. abt. throughout.
Pachycnema hippocastanaria.—C, on heaths nearly ev.
Gnophos obscurata.—N.F., ec. (heath form), T., M.; Ringwood, N. ;
Brockt., Hike; Burley,ai) c5 RB. Sotouy, x.,) 25 Che Hdlgce tami
Winton, c., V.; Portsdown, sc., Ps.; I.W.,c., 1. W.G., V., A.; Freshw.,
., Ht cPRe.
Ematurga atomaria.—Abt. nearly ev. on heaths, v. variable.
Bupalus piniaria.—Form flavescens of 3 ; c. in all pine woods ;
occ. white typical forms of g occur.
Selidosema plumaria (ericetaria).—N.F., c., M., K., T., ete.; less ec.
than formerly, A.; Brockt., Hk.; Ringwood, N.; Hayling, n. ¢., Ps.,
B. ; Woolmer, c., E.; 1.W., M1. B. di, ioe 826; nr. Ringwood, c., 5.; St.
(Biome, co 1909, 'L.W.N.H. S.
Tes doenanas vauaria.—©. ev. in gardens.
Lozoyramma petvaria.—Gen. dist., abt.
Chiasmia clathrata.—Gen. dist., more or less c. ; melanic forms and
vars. occur rarely.
Scodiona fayaria.—N.F., c., T., M., etc.; Ringwood, N.; Christeh.,
Dt.; Baddesley, r., F.; Ampfield, f. c., Ht.; Alton, S.; Woolmer,
Oe, lac
Aspilates gilvaria.—Hambledon, H.I'.C.; Formerly in a lane at
Southwick, Ps.; I.W., Cowes, J.W.G.
Aspilates ochrearia.—N.F., Ringwood, N.; Fdge., Ct.; Christch.,
Dt.; Higheliffe, A.; Ch. Fd., sc., R.: - Romsey, Pe. ; Fp es Tc, eke
H.; Portsdown, Hayling, C., Ps., . E.: SE AW goes ; Freshw., G., MW: ;
Gurnard: 18 2 St. Lawrence, Ce B.
Perconia pono tilaada ae ent! dist. on heaths, usually ce.
ZYGAENIDAE, ETC.
Zygaena viciae (meliloti).—N.F. only., v. loc., c. some yrs., M., D.,
F., etc.; Burley, Hk.; A few localities, in S.E. nr. New Copse and
Brockt., V.
LIST OF THE MACRO-LEPIDOPTERA, (35)
Zygaena trifolii.—Loe. c. throughout; prefers low-lying localities ;
ab. confluens c., ab, lutescens occ.; 1 chocolate-coloured sp. Hamble,
1917, Garner ; six-spotted sp. oceur.
Zygaena lonicerae,—This species is with difficulty separated from
the preceding; Gen. dist. and c.; prefers downs, and seems to be v.
invariable; I. W., no record.
Zygaena filipendulae.—Gen. dist. on downs, ete., ¢.; ab. flava occ.
at Winton, Ht., V.; ab. Azppocrepidis at Portsdown, c., Ps., B.; at
Netley, c., RB.
Adscita statices.—N.F., Church Place, f. c., Harris, A. ; Holmsley,
Ct.; Soton, loc. abt., F.; Eastleigh, f. c., se. lately, D., K.; Ch. Fd.,
e., R., A.; Ampfield, Ht; Winton, £. c., M.; Pismth.j v. loe.,:B. ;
Petersfield, loc. c., B.; Kingsclere, Sl.; 1.W., Shanklin, Hk.
Adscita geryon.—Winton, loc. abt., F., Ht., M., T., ete.
Cochlidion limacodes.—N.F., oce., M., T.; Ringwood, N.; Rbhamnor,
oce., H.R., VIII. 812; Wootton, Ct.; abt. in some parts of N.F., V.;
Soton district, sc., F., K., A.; Ch. Fd., sc., R.; Fareham, H.; Botley,
f. c., Garner; Ptsmth., oce., B. ; ae H.
Heterogena asella.—N.F., oce., M.; f.c¢., Ht., ; Ringwood, N.;
Chesbide ses, ehvs
Coes cosss.—Gen. dist. but n.¢.; at sugar, B. alc leec els W. «5
plentiful, 7.1V.G.
Aeuzera pyrina.—Soton, occ., M., K., F.; Winton, Ht.; Fareham,
oce., I’; Ptsmth., n. c.,.B.; Southsea, Hk.; Andover, Pamber, H. ;
TW.., f.-¢.,; 1.W.G.
Trochilium apiformis.—Christeb., H.F.C., Dt.; Ch. Fd., f. ¢., R.;
Bedhampton, e., Ps.; Petersfield, c., B.
Trochilium crabronifurmis.—Soton, Romsey, c., F.; Eastleigh, n. ¢.,
Ke; Wantoneeoce, Mo Sis Crossy & ¢.oHit. E.; : Alton, C., S: Liss,
Petersfield, abt., Ps., K.; Sth. of Newbury, Si. : I.W., Shanklin, feces
larvae in trunks of poplars, Sandown, [reshw., iis W.G.
Sctapteron tabanifurmis. —1 sp. nr. Cosham, 1908, B.
Aegeria (Sesia) s 1 sp., V.; Soton, loe: f. ¢., six
colonies, F.; Romsey, v. r., R.; Basingstoke, occ., M.; Pamber, f. co
Fe gl Wisy disp: ; Fareham; c:; T:3 Havant, o, E.;
Little Park, Hk.; I.W., Brading, Ryde, Bordwood, J.W.G., Freshw.,
Tutt., Brit. Lep., V. 884.
Marasmarcha linaedactyla (phaeodactyla).—Hythe, A. ; Winton, e.,
F.; I.W., coast, Vent., Tutt, Brit. Lep. V. 404. .
Amblyptilia cosmodactyla (acanthodactyla).—Alton, H.F:C.; N.F.,
Bnmth., Portsea, 1.W., Vent., Tutt, Brit. Lep., V.297 ; Ryde, Sandown,
I.W.G.
Eucnaemidophorus rhododactyla.—Oceurs, H.F.C. (a doubtful
record).
LIST OF THE MACRO-LEPIDOPTERA. (39)
Gillmeria. (Platypttlia) pallidactyla (bertrami).—Bumth., R.; Soton,
los. c., .F. ;. Eastleigh, loc. c, K.: Ch. Fd., sce., R.; Winton, foc, K. ;
Portsdown, as ae Aldershot, Ispeyonte: it W., Vent., Tutt, Br. Lep.,
VY. 250.
Gillmeria (Platyptilia) ochrodactyla.—N.F., E.R., XXIV. 171;
Boscombe, R.; Occurs, H.F.C.; These records probably all refer to the
preceding species;, See Tutt, Br. Lep., V. 235.
Platyptilia gonodactyla.—Soton, r., F.; Hastleigh, oce., K.; Ch.
Fd), so, R.i 1.W:, Coast, c.,,V.; Vent., n.c., Tutt, Br. Lep., V. 218;
Sandown, J.W.G.
Capperia (Oxyptilus) heterodactyla (teucrit)—N.F., Hk., Tutt;
Boscombe, R.; Hayling, f.c., V.
aiid parvidactyla.— Winton, loc. c., F., K., Cr.; Fawley Down,
; I.W., Coast, abt., V.; Vent., Tutt, Br. bic. We 434: Sandown,
7 - G.
Wheeleria (Aciptilia) megadactyla (spilodactyla)—I.W., Cr.;
Freshw., c., T., etc. ; Chalk Downs, loc. abt., V.
Wheeleria (Aciptilia) niveidactyla (baliodactyla).—Bnmth., R.; I.W..,
c., Ent., XVL. 270; Brading Down, I.W.G.
Merrifieldia (Aciptiiaa) tridactyla (tetradactyla).—Farley, n. ¢., R. ;
Winton,.f. ¢.,.H\,; L.W.., C.
Buckleria (Aciptilia) Aen: = N.E:, lay, Putt, Br. Lep,, Vi 516 ;
Nr. Whitley Wood, Hnt., 1911, p. 368; Bnmth., Bialiben VILL. 270;
Woolmer, V.
Oidaematophorus lithodactyla.—Bnmth. coast, H.F.C.; Ch. Fd., se.,
R. ; River Ltehen, c., F., K.; Fisher’s Pond, c., K.; I.W., Sandown,
I.W.G., Yarmouth, Hnt., 1889, p. 236.
E'mmelina (Pterophorus) monodactyla.—Abt. probably ev.
Leioptilus tephradactyla.—Occurs, H.F.C.
Leioptilus carphodactyla.—I.W., Sandown, 2 sp., 1907, in fair
numbers 1908, J.W.G@.
Ovendenia (Letoptilus) septodactyla (Llieniyianus).—Vent., H.E.C.,
Staintows Manual.
Adaina (Leioptilus) microdactyla.—Oceurs, H.F.C.; [.W., Coast, V. ;
Sandown, Bembridge, .W.a.
Hellinsia (Letoptilus) osteodactyla.—Coast, H.F.C.; Portsdown,
WSs es:
Porrittia (Aciptilia) galactodactyla.—n. ¢., H.F.C.; Soton, f. ¢., F.;
Ch. Fd., f.; Mottisfont, A.; Eastleigh, Fisher’s Pond, loe, ¢., F., K.;
Winton) tice te wetsng the loescomheed) ~ Allon) loca CoH). uals WN.
Seaview, A. .
Alucita (Aciptilia) pentadactyla.—e. probably ev.
_ Orneodes (Alucita) hexadactyla.—yv. ¢. ev.
CramBI.
Chilo phragmitellus.—Christch., H.F.C.; Havant, c., H., T.; 1.W.,
Brading Marshes, 1.W.G.
Schoenobius forficellus—N.F., c. in bogs, V.; Denny Bog, Cr. ;
CGhvistch., H:F.C, ; Ch; Fd., f. c., B.; Fisher’s Pond, Ce hess ai:
Brading, 1.W.G.
Schoenobius gigantellus.—Christch., H.F.C.; 1.W., Brading, 1 sp.,
LEVER G Ri:
Calamotropha paludella.—Occurs, H.F.C.
(40) THE ENTOMOLOGIST’S RECORD.
Platytes cerussellus.—Hayling, I.W., v. abt., V.; Culver, I.W.G.
Crambus alpinellus.—Hayling, V.; I-W., St. Helens; loc. -e:,
T.W.N.H.S., Cr. wel i |
Grants falsellus. —Oceurs, H.E.G., Ving I.W., Sandown, 1 8p
LE WEG:
Crambus pratellus.—c. Bene ev.
Crambus dumetellus.—Ly., H.F.C., Stainton ; Soton, v. r., F.; Ewes
old records only.
Crambus sylvellus.—N.F., loc. abt. in bogs, V.; Ly., H.F.C.;
Beaulieu, c., R., Cr. ; Ch. Fd., Va JB
Crambus hamellus,—N.F. , freely nr. liye) Vins Bewalion Ra iesCr.;
Matley, sc., R.; Ch. Fd., sc., R.
Cranatnis acon OND LEN, c., T., Cr.; Soton, abt., F.; Ch. Fd. | c.,
R., Cr. ; abt. in damp places, V.
Crambus uliginosellus.:—N.F., abt. in bogs V. R.; Beaulieu Rd., Cr: ;
Boscombe, Ch. Fd., c., R.; Woolmer, c., E.
Crambus pinellus.—N.F., V.; Wood Fidley, Cr.; Baddesley, f. c.,
Hye SOLO Vance PAT qs Chashices f. Ce RR SmWis Sandown, LW.G.
Crambus latistrius: —N.F., Ly., V., HLE.C., Jase ¢ Minstead, 1 sp., Cr. ;
Ch. Fd.,c., R.; Hayling, abt., V.; 1 W., Sandown, locsers LW.G.
Crambus porlellus. 6, nearly eV. ; var. varringténellus, in N.F.
Crambus selasellus.—N.F., Hk.; Ly., H.F.C.; Matley, R. ; Christch.,
oj as B Shoals Tay CH, Olng Nth Avo Ga. ito, Ole. '8 Hayling, ey » Bs I.W.,
Sandown, loc., Brading, 1.W.G.
Crambus tristellus.—c. nearly ev.
Crambus fascelinellus.—I.W., Yarmouth, 1 sp., Stainton; abt. in
one locality in Hants in 1886, not seen since, H.F.C.
Crambus inquinatellus.—e. nearly ev.
Crambus contaminellus.—I.W., St. Helens, [.W.N.H.S., Cr.
Crambus geniculeus.—Abt. ev., V.; Ch. Fd., f. c., R.; Soton, e., F.;
Havant, c., E.; I.W., Ryde, Bembridge, abt., Freshw., c., Shanklin,
TW.G.
Crambus culmellus.—Abt. ev.
Crambus chrysonuchellus.—Mottisfont, Cr.; Farley Mt., n. c., F.;
Portsdown, n. c., T.; Havant, n. c., E.; I.W., loc. abt., V.; Downs
above Steephill Castle, f. c., Freshw. Downs, f. c.,'J.W.G.
Crambus hortuellus.—e. nearly ev.
Kromene ocellea,—N.F., 1 sp., 1899, A.
Anerastia lotella. Soon, c. on sandhills, R- Hythe, A.;
Hayling Sandhills, c., E.; I.W., St. Helens, Cr. |
Llithyia ER Wanlicn pore W., ‘Bembridge, LW. Gs Vent., loc. c.,
Freshw., r., A.
Maloehia cribrum.—N.F., Beaulieu, H.F.C.; Christch! EH. ;
Solon isc Muh Cha Hideisnwecesn Ey: - Rastleigh, eel Gay JEG, 8 Havant, Cx
He Ws old records only.
bFlonoeacon sinuella.—N.F., Beaulieu Rd., Cr.; Portsdown, Ps. ;
I.W., Sandown, abt., V.; Vent., abt., Limpet Bun, L.W.G.
Homoeosoma i Aiba —Hayling, I.W., Shanklin’ V.; Sandown,
L.W.G.
Homoeosoma binaevella.—Ch. Fd., sc., R.; 1.W., Sandown, /.W.G.
Hlomoeosoma senectonis—-I.W., Cr.
Ephestia elutella.—Occurs, V., H.F.C., Ch. Fd., n.¢., R.; LW., St.
Helens, J.W.N.H.S.
Vou. XXXVI. Puate I.
The Entomologists’ Record.
Somatic Mosaics.
Vou. XXXVI. Puatr IT.
The Hntomologist’s Record.
TreratToLocicaL Lees in LEPIDOPTERA.
I, Apocheima hispidaria. 6 & 7. Lycia hirtaria.
2&3. Lasiocampa trifolii. 8 & 9. L. trifolii.
4&5. A. hispidaria.
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