vey 5 1 $y a] MEAT aut states pe nating, 4 Pete Whee eke aes Se ee ee eee eS Eee eee : ’ gin Agvet ; wits x i H's Aten f . ; ? a i dies i RPT A ‘ths, : Er Anan farts REM er saeat —-** " | ; i ‘ : ‘ , de J ‘ | 4 -% ; 4 ‘ ¢ Tea ye Ns ' tt te H . ‘ by . 3 ; Niece ; ittbrels 3 i ‘ re G * Aa ere ' j ‘ 4 n : 7 ae : . i Ast deeb ke , , : win t epee i +m , Shoat eas t 5 ‘ Ree, dieses eee ener? i aa fie se Pao a eH eart and a mee hag we ah M WW Wen ag 5 U ay on Deka raat, Nee Sah gee’, U4 uy ‘ ~/ THE ENTOMOLOGIST An Illustrated Journal OF 4 AS ee GENERAL ENTOMOLOGY. ‘- A Gow EDITED BY RICHARD SOUTH, F.E.S. WITH THE ASSISTANCE OF ROBERT ADKIN, F.E.S. C. J. GAHAN, M.A., F.E.S. H. ROWLAND-BROWN, M.A., F.E.S. W. J. LUCAS, B.A., F.E.S. W. LUCAS DISTANT, F.E.S., &c. CLAUDE MORLEY, F.E.S., F.Z.8. F. W. FROHAWK, F.E.S., M.B.O.U. Dr. D. SHARP, F.R.S., F.E.S., &c. ‘ By mutual confidence and mutual aid Great deeds are done and great discoveries made.’ VOLUME THE FORTY-SEVENTH. / SA se LONDON: WEST, NEWMAN & CO., 54, HATTON GARDEN. SIMPKIN, MARSHALL, HAMILTON, KENT & CO., Liurtep. 1914. CaP iy a rm te OY \ a uy Wr ap a “ Ps i of Y : Y ¢ ny at bs, Vy J “LIST OF CONTRIBUTORS. ANDERSON, J., 301 ARKLE, J., 206, 226 AustEN, E. E., 70 Baker, H. W., 324 Barrett, C. G., 277 BaRRett, J. Puatr, 132, 152, 226 BETHUNE-BAKER, G., 39 Bouam, GrorGs, 71, 251 Boyp, A. W., M.A., 112, 135 BrackEn, C. W., B.A., F.E.S., 96, 131 Brinviey, H. H., 65 Brock, 8. E., 105 Brown, F., 277 Bucxuurst, A. 8., 225 Bourras, A. L., 277 Buss, A., 40 Buxton, P. A., 206 Campton, F. W., 63 Campton, H., 63 Carr, J. W., M.A., F.L.S., F.G.S. 66, 95 Carr, L. A., 205 Cuapwick, L., 152 Cuarman, T. A., M.D., F.E.S., 218 Cuartss, S. A., 106 CiutTrerBuck, C. GRANVILLE, F.E.S., 40, 106 CocxkERELL, Prof. T. D. A., 32, 114, 131, 142, 191, 197, 213, 242, 305 Coney, B. A., 105 Corset, A. 8., 151 Davin, E. ee a 39 Daws, W., 224 Distant, W. L., 87 Dotton, H. ie, 40, 204 E\petstTeEn, H. M., 71 Exeter, A. J., 41 Fett, EK. P., 86 Frouawk, F. W., M.B.0.U., F.E.S., 179, 212, 301 Fryer, J. C. F., M.A., F.E.S., 300 Ganan, C. J., M.A., F.E.S., 160, 188 Gripes, A. EH., F.L.S., F.E.S., 54 Giravtt, A. A., 53, 68, 197 Goon, R. D., 300 GuRNEY, GerRARD H., F.E.S., 147, 173, 278, 301 HAINES; ) eee, | DIPSH.,, M.R.C:S., L.R.C.P., 129, 146, 224 Hamer, S. H., 151 Harovine, M. J., 277 _., Harrison, J. W. H., B.Sc., 92 Hicks, JouN Be oo; 72, 207 = Hones, Harotp, 39, 252, 279, 325 Houamns, A. W., 325 Hont, H. £., 104 Honter, R. L., 204 Jackson, F. W. J., 300 JEDDERE-FIsHER, H. C., 277 Keusaui, The Rey. J. E., 40 KersHaw, G. Bertram, 38 Legs, A. H., 225 Lowe, Rev. F. E., M.A., F.E.S., 14, 60 Lucas, W. J., B.A., F.E.S., 77, 97, 112, 143, 180, 190, 203, 230, 252, 256 Louvonr, A. B., 99 yim, GT, EELS... 73, 105, 119) 2a, 287 Macminuan, W. W., 131 ManssripGE, W., 48, 72, 109, 136, 183, 208, 328 Maruev, G. F., F.L.S., F.E.S., 42, 113, 132 Metpora, Prof. R., D.Se., LL.D., F.R.S., &e., 225 Metiows, C., 131, 180 MetcanFe, Rev. Joun W., F.E.S., 244 Moraan, D., 206, 301 Morey, CuavubE, F.Z.S., F.H.S., 23, 37, 137, 170, 184, 215, 225 Morton, KennEtH J., F.E.S., 1, 49, 209 Neave, B. W., 181 Nevinson, E. B., 299 OupakER, Rev. F. A., M.A., F.E.S., 276 Outver, G. B., 325 PickarD-CamBRiIpGE, A. W., 206 Puiu, H. V., 152 PripEaux, R. M., F.E.S., 228, 253, 303 Ramsey, L. N. G., M.A., B.Se., 20 Ret, P. C., 39, 274, 277 Rensuaw, G. B., F.E.S., 299 Ricuarps, Percy, 205 Riuey, Norman D., F.E.S., 48 Rippon, C., F.E.S., 251 Rosertson, Major BR. B., 106 Rosinson, A., 253 Roruscuitp, The Hon. N. C., M.A, F.L.S., F.E.S., &e., 7 RovurnepGe, GEorGE B., F.E.S., 225 Rowxianp-Brown, H., M.A., F.E.S., 8, 34, 41, 55, 87, 126, 177, 180, 185, 207, 281, 301, 304, 308 Sr. Joun, W. S. A., 324, 326 Sane, G. B., 71; 107 Suarp, EH. P., 106 Surupon, W. G., F.E.S., 82, 141, 152, 224, 233, 269, 293, 315 Sutra, R. 8., 324 Soury, Ricuarp, F.L.S., 106, 136, 180, 183, 205, 208, 224, 225, 230, 231, 232, 255, 280, 324 iv Spruuer, A. J., 251 Stirr, Rev. T. A., 323, 324 STowE LL, EK. N. C., 38, 39 Strupp, E. F., 181 Taytor, W. R., 180 THEOBALD, F. V., M.A., F.E.S., &c., 28, 36, 100 THURNALL, A., 313 Turner, H. J., 47, 109, 135, 159, 182, 208, 229, 280, 303, 327 Tyrrman, W. A., 40 INDEX. WHEELER, Rev. G., M.A.. 45, 108, 158, 182 WHIcHER, S., 251 WuirtincHam, Rev. 297, 325 Wuemay, A. E., F.E.S., 161, 201, 219, 266, 290, 318 Wit11am, B. S., 181 Wiutiums, C. B., B.A., F.E.S., 51, 247, 249, 262 WiuuraMs, H. B., 328 Wiuiams, J. W., 252 W.. Goyehebesss Warp, J.D., 40 Winston, St. A. Sv. J., M.B.C.S., Wuatn, C. W., 106 M.R.C.P., 326 PLATES. PAGE I { Meteorus albiditarsis, M. niger, M. fragilis and cocoons of ) to. face 73 six species of Meteorus . : : Il.—Sympetrum striolatum x 77 IlI.—Erebia ligea, var. adyte, Hb., franciion to topical aged: it. * 113 | Wicken Fen as it is. ] IV 1. Reed bed near Wicken Village shows HB opel HE ee is 185 2. A ‘*Load’’ in the Fen } V.—Hemerobiid Wings 3 : Fy 209 VI. ( Macrocentrus marginator, Zele infumator, Z. discolor, 257 Z. testaceator, and cocoons of four species : VII.—At Le Lauteret. A Haunt of P. thersites . “ 4 : " 305 ILLUSTRATIONS IN THE TEXT. Sympetrum striolatum (lateral thoracic markings) ; é ¢ : 4 Three figures illustrating oviposition of Rhyssa : 2 ; : : Age el Rectinasus buxtoni, sp. nov. 29 Forda rotunda, sp. nov. 31 Tyrbula scudderi 5 33 Metanea chapmani {a cn of aldomen from above L. é : . Ba) Chirothrips frontalis, sp. nov. Head and prothorax . : é : + be Forficula auricularia : . 65 Ascalaphus coccajus. Pupa-skin 97 Argynnis selene, aberration 113 Arctia villica, aberration . 113 Diestrammena marmorata, female 145 Psephenoides immsi sp. nov. 188 Kakothrips robustus . 247 Podagrion pachymerum 264, 265 INDEX. oe GENERAL. Aberrations of Argynnis selene and Arctia villica, 113 Acronycta menyanthidis emerging in November, 40 Acronycta strigosa, &c., in Cambridge- shire, 313 Aphididw, Additions to the list of Kent, 100 Araschnia levana in Herefordshire, 325 Arctiade, New species of, from Formosa, 161 Atlantic forms of Sympetrum striola- tum, Some remarks on, ol Bee resembling a Wasp, A, 142 Bees, Australian Halictine, 242 Bees, Australian, of the Genus Eury- glossa, 213 Bees, New Australian, 197 Bees, New and little known, 114 Bees, Some Tasmanian, 305 Braconide, British, Contribution to our knowledge of, 78, 119, 257, 287 Butterfly collecting in Sicily and Cala- bria in 1912 and 1913, 132, 152 Butterfly Hunt in some parts of Un- explored France, A, 8, 55, 87, 126 Butterflies of Derbyshire, 324 Butterflies of Venice and Neighbour- hood, 206 Butterflies, Russian, An Expedition in search of, 233, 269, 293, 315 Cerura bifida in August, 277 Chalcid Parasite of Mantis eggs, Poda- grion pachymerum, Notes on, 262 Cicada, Description of a new, from W. Africa, 87 Coleoptera, Eggs of Prionus coriarius, 252; of Norfolk, 180; of the Family Psephenide, a new Genus of, 188 Cordulegaster annulatus in the Nymph Stage, 325 Courtship of Gomphocerus maculatus at Craigton (Linlithgowshire), Notes on, 104 Crambi, A successful hunt for some of our local, 244 Cyaniris argiolus in §S. E. Sussex, Abundance of, 276 Dauphiny, Three weeks in, 281, 308 Delamere Forest, A day in, 226 Dermatobia in Guatemala, 131 ‘‘Do houseflies hybernate ?”’ 69 Dragonflies bred in 1913, 39; in 1914, 278 Dragonfly at Sea, A, 39, 72 Dragonfly season of 1913, Notes on the, 63 Earlier stages of Colias hecla, The, 82 Karly pupation of Lasiocampa quercus, 324 Eggs of Prionus coriarius (Coleoptera), 252 Emergence : Acronycta menyanthidis in November, 40; of Conchylis gigan- tana (alternana), 297; Harly, of Smerinthus ocellatus x Amorpha populi (hybridus), 251; Retarded, of Pararge egeria, 106, 131; of Saturnia pavonia (carpini), Delayed, 104 Entomological jottings from Chichester, 301 Entomological trip to Corsica, An account of an, 147, 173 Entomology of Helianthus, The, 191 Euchloé cardamines, Appearance of, 225; Harly appearance of, 206; Two years in pupa, 181 EKurois occulta in Essex, 323 Formaldehyde useful in setting insects, 325 Fossil Orthoptera of Florissant, Colo- rado, The, 32 Garden Notes, 215 Geometride, New Formosa, 201, 290 Grasshoppers, Tropical, in England, 131 Gynandromorphous bred specimens of Catopsilia (Callidryas) crocale, 204 Gynandrous P. icarus, 277 species of, from Hemiptera of Norfolk, 180 Hesperiids, European, Notes on, 141,177 Hibernation of Pyrameis atalanta, 151, 181; of the larve of Lycena argiades, 179 vil INDEX. Hymenoptera, Dorset, 129; submitted for determination, 225 Insects, Continental, of various orders taken by Dr. Chapman in 1913, 97 Larva of Thecla spini, Description of a full fed, 152 Larve of Acherontia atropos near Nor- wich, 277 Larve of Zygena exulans, Notes on the, 180 Late appearances of Acidalia emutaria and 'l’oxocampa pastinum in Lincoln- shire, 324 Lepidoptera of La Sainte Baume, S. France, Some notes on the, 14, 60 Life Histories of Hesperia tessellum and H. cribrellum, 7 Locauiries :-— Africa, W., 87; Algeria, 28; Alps, Basses, 180; America, C., 54; Ame- rica, S.,51; Ashby-de-la-Zouch, 277; Australia, 197,213,242; Australia, N., 197; Berkshire, 204; Calabria, 132, 152; Cambridgeshire, 313; Chi- chester, 301 ; Colorado (Florissant), 32; Cornwall, 224; Corsica, 147, 173, 224; Cumberland, N., 225; Derbyshire, 324, Devon, 323; Dorset- shire, 129, 146, 300; Dovedale, 39, 106; Hastbourne, 106; Epping Forest, 104; Essex, 41, 323; Felix- stowe, 301; Formosa, 161, 201, 219, 266, 290, 319; Forest of Dean, 325; France, 8, 49, 55, 87, 126; France (La Sainte Baume), 14; France (Vercors, Dréme), 13; France (Villars de Lans, Isére), 13; Glamorganshire, 39; Gloucestershire, 40, 105, 106 ; Guatemala, 131; Hants, 39, 40, 277; Herefordshire, 325; Kent, 40, 100, 205, 224, 301; Lanes, 40; Lincoln- shire, 324; Linlithgowshire (Craig- ton), 104; London, N.W., 204; Middlesex, 41; Norfolk, 277, 324; Norwich, 277; Nottinghamshire, 63, 95, 223; Queensland, 53; Russia, 233, 269, 293; Salcombe, 70; Samoa, 36; Shetland, 274; Sicily, 132, 152; Skye, Isle of, 106; Sussex, S.K., 276; Venice, 206 ; Wicken Fen, 151, 218, 252, 298, 299; Worcestershire, 251 Lycenidex, The Sleeping attitude of, 212 Melanic female of Biston hirtaria, 180 Metamorphosis of Phasgoneura viridis- sima, Notes on the, 99 Middlesex Lepidoptera in 1914, Abun- dance of, 301 Mildness of the past season, Note illus- trating, 38 Monograph of the Genus Acroricnus, A, 170; Joppidium (Walsh), A, 137; Osprhynchotus (Spinola), A, 23 Mosquito from Samoa, A new, 36 Moths captured by light trap, 227, 253, 302 Moths casually passing more than a year in the pupal state, 71 : Myrmecophilous Aphides from Algeria, Two new, 28 Neuroptera, British in 1913, 190; Con- tinental, 203; of Nottinghamshire, The, 66 New Central American Syntomide, 54 New Genus of Miscogasteridew (Hymen- optera Chalcidoidea), 68 New Species of Chirothrips (Thysan- optera) from S. America, A, 51 New Species of Eurytoma from Queens- land which lives in the stems of Eucalyptus, A, 53 New species of Metancea from France, A, 49 Noctuide, New Species of, from For- mosa, 161, 219, 226, 319 OxrruaRy :— Bloomfield, Rev. E. N., 184 Corbin, George, Bentley, 160 Dobson, H. T., 256 Warren, William, 303 Odonata, 96 Odonata, Continental, 203 Odonata, British, in 1913, 77 Orthoptera, British, in 1913, 143 Oviposition of Rhyssa, Note on the, 20 Pairing of Moths, Unusual, 38 Pecilopsis (Harrison), The Genus, 92 Plutella maculipennis (cruciferarum), Abundance of, 205, 225 Prolonged pupal duration in Eriogaster lanestris, 152 Psocidse of Nottinghamshire, The, 95 Rearing Dasypolia templi, Note on, 38 Recent Lirerature :— Annals of Tropical Medicine and Parasitology, 112 Catalogue of the Lepidoptera Pha- lene in the British Museum, vol. xlii., by Sir G. F. Hampson, Bt., 208 Common British Beetles, by Rev. C. A. Hall, F.R.M.S., 231 Common British Moths, by A. M. Stewart, 48 Contribution towards a Monograph of the Homopterous Insects of the Family Delphacide of North and South America, vol xlvii., 232 Descriptions of twenty-three New Genera and thirty-one New Species of Ichneumon Flies, by H. L. , Viereck, 232 Etudes de Lépidoptérologie Comparée, Fasc. ix. lve et 2e Parties, 304 INDEX. Vii Hymenoptera, Superfamilies Apoidea and Chalcidoidea, of the Yale- Dominican Expedition, by J. C. Crawford, 256 Memoirs of the Queensland Museum, 136, 208 Memorias do Instituto Oswaldo Cruz, vols. 5-6, 280 Monograph of the Jumping Lice or Psyllide of the New World, by D. L. Crawford, 255 Names applied to the North American Bees of the Genera Lithurgus, Anthidium, and Allies, by T. D. A. Cockerell, 256 New Genera and Species of Micro- Lepidoptera from Panama, by A. Busck, 256 New Hymenoptera from North America, by A. B. Gahan, 256 New Species of Noctuid Moths from Tropical America, by W. Schaus, 232 North American Springtails of the Subfamily Tomocerine, by J. W. Folsum, 232 Pond Problems, by E. E. Unwin, M.Se., 255 Proceedings of the South London Entomological and Natural History Society for 1913-14, 232 Proceedings of the United States National Museum, vols. xlvi., xlvii., 232 Revision of the Ichneumonidex, Based on the Collection in the British Museum, with descriptions of New Genera and Species, 230 Studies on the Mecoptera of Japan, by T. Miyake, 229 The Forty-third Annual Report of the Entomological Society of Ontario for 1912, 112 The Journal of the Board of Agri- culture of British Guiana, vol. vii. 232 The Life of the Fly, by J. H. Fabre, 159 The Life of the Spider, by J. H. Fabre, 159 The Noctuid Moths of the Genera Palindia and Dyomyx, by H. Dyar, 256 Transactions of the City of London Entomological and Natural History Society for 1911, 1912 and 1913, 48, 231 Type Species of the Genera of Ich- neumon Flies, by H. L. Viereck, 231 Reversion of Arctic Hrebia ligea, &., 34 Rhopalocera taken and observed at Villars de Lans (Isére), and in the Vercors (Dréme), List of, 13 Scelionid Parasite of Locust’s Eggs from the Northern Territory of Australia, A new, 197 Socrnrins :— Derbyshire Entomological, 136 Entomological of London, 43, 107, 156, 181 Lancashire and Cheshire Entomolo- gical, 47, 72, 109, 135, 182, 208, 328 London Natural History, 327 Manchester Entomological, 109, 135 South London Entomological, 45, 108, 134, 158, 182, 207, 228, 279, 303, 326 Sphinx convolvuli in Norfolk, 324 Stomoxys at a high altitude, 131 Synpherobius (Hemerobius), Notes on the British Species of, 209 Synonymy of Ichneumon obliteratus and I. barbifrons, 37 Thysanoptera, Kakothrips, n. gen., A Division of the Genus Frankliniella, 247 VARIETIES :— Agriades corydon, 180 Chrysophanus phleas, 277 Gonodontis bidentata, 132 Lycena corydon, 251; icarus, 251 Pyralis costalis, 131 Zygena transalpina, 205 *Verrall Supper,”’ The, 71 Viviparous British Beetle, Phytodecta viminalis, 249 Wasps active in December, 39 Wicken Fen, Its Conservation for Entomology, 185 Xanthorhoé galiata var. unilobata in Devon, 323 SPECIAL iN Dl xX. New Genera, Species, Sub-Species, and Varieties are marked with an asterisk. Order PROTURA. Acerentemon, 157 Acerentulus, 182 Order ZORAPTERA, p. 157. Order I. COLLEMBOLA, p. 184. Order VII. ORTHOPTERA. Agathemera, 32 marmorata (Diestrammena), 144, 145 Anabrus, 32 minor (Labia), 144 auricularia (Forficula), 65 multispinosa (Tyrbula), 33, 34 auricularia, var. forcipata (Forficula), | Orchelium, 32 66 Paleorchnia, 32 bicolor (Stauroderus), 144 parallelus (Chorthippus), 143, 144 bipunctatus (Tetrix), 144 Photina, 34 brachyptera (Metrioptera), 144 phymateus (Aigrotera), 229 Capnobotes, 32 punctatissimus (Leptophyes), 144 carolina (Stagomantis), 265 quadripunctata (Phaneroptera), 131 cinereus (Thamnotrizon), 143 religiosa (Mantis), 262, 263, 265 *costalis (Lithophotina), 34 rufipes (Omocestus), 98, 144 falcata (Phaneroptera), 131 rufus (Gomphocerus), 144 floccosa (Lithophotina), 34 *scudderi (Tyrbula), 33 gigantea (Forficula), 300 Stagmomantis, 34 griseo-aptera (Pholidoptera), 143, 144 sylvestris (Nemobius), 144 grossus (Mecostethus), 143, 144 Teniopodites, 32 Gryllacris, 32 texana (Stirapleura), 33 Ischnoptera, 32 Tyrbula, 33 Labiduromma, 32 viridissima (Phasgonura), 99, 143, 301 lineatus (Stenobothrus), 144 viridulus (Omocestus), 143, 144 Lithymnetes, 32 vulgaris (Gryllotalpa), 229 maculatus (Gomphocerus), 104, 105, 143, Zetobora, 32 144 Order VIII. PLECOPTERA. marginata (Nemoura), 97 variegata (Nemoura), 98 cinerea (Nemoura), 97 inconspicua (Nemoura), 98 lateralis (Nemoura), 98 Order IX. PSOCOPTERA. burmeisteri (Cecilius), 96 cruciatus (Graphopsocus), 95 cyanops (Elipsocus), 95 abietis (Elipsocus), 95 bifasciata (Amphigerontia), 95 briggsi (Ectopsocus), 96 INDEX. 1X divinatorius (Troctes), 96 fasciata (Amphigerontia), 95 flavidus (Cecilius), 96 flaviceps (Philotarsus), 95 guestfalicus (Hyperetes), 96 immaculatus (Stenopsocus), 95 longicornis (Psocus), 95 nebulosus (Psocus), 95 pedicularia (Pterodela), 96 unipunctatus (Mesopsocus), 95 variegata (Amphigerontia), 95 westwoodi (Elipsocus), 95 Order X. ISOPTERA. lucifugus (Leucotermes), 30 Order XIII. zenea (Cordulia), 39, 77, 98 annulatus (Cordulegaster), 39, 64, 78,79, 204, 278, 325 brunneum (Orthetrum), 98 cerulescens (Orthetrum), 63, 78, 96, 203 cancellatum (Orthetrum), 78, 96 cyanea (Aischna), 79 cyathigerum (Enallagma), 64, 77, 78, 98, 278 depressa (Libellula), 64, 78, 203 dubia (Leucorrhinia), 78, 226 elegans (Ischnura), 39, 64, 77, 78, 98, 278 elegans, var. rufescens (Ischnura), 78 ephippiger (Hemianax), 79 fonscolombii (Sympetrum), 78, 79 fulva (Libellula), 64 grandis (Aischna), 39, 79, 278 hemorrhoidalis (Calopteryx), 204 hafniense (Brachytron), 64 hastulatum (Agrion), 78 imperator (Anax), 78, 79 isosceles (Aischna), 79, 98 juncea (Aischna), 79, 98, 226 mercuriale (Agrion), 78, 79, 204 meridionale (Sympetrum), 96 metallica (Somatochlora), 63 mixta (Aischna), 79 naias (Hrythromma), 39, 64, 78, 278 ODONATA. { = PaRANEUROPTERA. | nymphula (Pyrrhosoma), 39, 63, 64, 77, 78, 98, 204, 218, 278 pennipes (Platyenemis), 63, 78, 204 pratense (Brachytron), 278 puella (Agrion), 63, 64, 77, 78, 218, 278 pulchellum (Agrion), 64 pumilio (Ischnura), 78, 79 quadrimaculata (Libellula), 39, 64, 77, 98, 278 ruficollis (Libellula), 1 scoticum (Sympetrum), 2, 72, 79 splendens (Calopteryx), 64, 203 sponsa (Lestes}, 78, 278 striolatum (Sympetrum), 1, 2, 3, 6, 7, 39, 64, 78, 79, 80, 81, 96, 278 striolatum, var. nigrescens (Sym- petrum), 2 striolatum, var. nigrifemur (Sym- petrum), 1, 2, 3, 7 tenellum (Pyrrhosoma), 63, 78 tenellum, var. melanotum (Pyrrhosoma), 78 uncatus (Onychogomphus), 203 virgo (Calopteryx), 39, 63, 64, 78, 79, 203, 278 vulgatissimus (Gomphus), 39, 78 vulgatum (Sympetrum), 3, 81, 96, 98 Order XIV. THYSANOPTERA. cephalica (Frankliniella), 248 Chirothrips, 51 crassus (Chirothrips), 52 floridensis (Frankliniella), 248 Frankliniella, 51, 247, 248 *frontalis (Chirothrips), 51, 52 fusca (Frankliniella), 248 gosypii (Frankliniella), 248 hamatus (Chirothrips), 52 helianthi (Frankliniella), 248 insularis (Frankliniella), 248 intonsa (=vulgatissimus) (Franklini- ella), 248 Kakothrips, 247, 248 manicatus (Chirothrips), 53 melanommata (Frankliniella), 248 mexicana (Chirothrips), 53 minuta (Frankliniella), 248 nervo3us (Frankliniella), 248 nobilis (Megathrips), 248 obesus (Chirothrips), 52 occidentalis (Frankliniella), 248 Physopus, 248 Physothrips, 51 pisivora (Thrips), 247 robusta (Euthrips), 247 robusta (Frankliniella), 247, 248 robusta (Physopus), 247 robustus (Kakothrips), 248 runneri (Frankliniella), 248 similis (Chirothrips), 53 stylosa (Frankliniella), 248 sulphurea (Frankliniella), 248 tenuicornis (Frankliniella), 248 Thrips, 51 tritici (Frankliniella), 196, 248 b INDEX. Order XV. HEMIPTERA. affinis (Scolopostethus), 146 agilis (Hulachnus), 103 agilis (Pachnus), 103 agilis (Stenocephalus), 146 albomarginatus (Gnathoconus), 146 ambiguus (Psallus), 147 ambrosie (Macrosiphum), 196 angustulus (Ischnocoris), 146 apterus (Halticus), 147 aquilegie (Macrosiphum), 102 arbustorum (Plagiognathus), 147 arundinis (Macrosiphum), 102 ater (Rhopalotomus), 147 beccabungee (Aphis), 102 bet (Macrosiphum), 101 betule (Vacuna), 103 betuleti (Psallus), 147 bidens (Picromerus), 146 bidentata (Pygolampis), 207 binotatus (Stenotus), 147 bipunctatus (Calocoris), 147 bumeliz (Brysocrypta), 103 *buxtoni (Rectinasus), 29 calcaratus (Miris), 147 campestris (Lyctocoris), 147 cervinus (Lygus), 147 chiragra (Rhyparochromus), 146 cincta (Salda), 147 cinerea (Nepa), 147 citri (Pseudococecus), 207 claviculus (Cymus), 146 cocksi (Salda), 147 coerulea (Zicrona), 146 contractus (Notochilus), 146 coriaceus (Chaitophorus), 103 corticalis (Chermes), 182 coryli (Phylus), 147 crategarium (Macrosiphum), 102 currens (Velia), 146 decoratus (Scolopostethus), 146 denticulatus (Coreus), 146 depressus (Aradus), 146 diplanterer (Macrosiphum), 102 dolobrata (Leptopterna), 147 duffieldii (Macrosiphum), 101 dumosa (Jalla), 158 elegantula (Microphysa), 147 ericetorum (Nabis), 146 ericetorum (Orthotylus), 147 fagi (Phyllaphis), 229 fallenii (Psallus), 147 ferrugata (Leptopterna), 147 flavomarginatus (Nabis), 146 flavonotatus (Cyllocoris), 147 foeniculi (Siphocoryne). 103 fraxini (Phyllopsis), 229 fraxinicola (Phyllopsis), 229 galii (Aphis), 102 geminatus (Ischnorhynchus), 146 geoffroyi (Corixa), 147 gibbifera (Gerris), 218 gigantea (Musoda), 87 glandicolor (Cymus), 146 glauca (Notonecta), 147 gossypii (Aphis), 102 gothicus (Lopus), 147 graminis (Macrosiphum), 101 griseus (Hlasmostethus), 146 hemorrhoidale (Acanthosoma), 146 helianthi (Aphis), 196 hieroglyphica (Corixa), 147 histrionicus (Cyllocoris), 147 holsatus (Miris), 147 .humuli (Monanthia), 146 infusus (Calocoris), 147 interstinctum (Acanthosoma), 146 inule (Phorodon), 103 inuncta (Podops), 146 juniperi (Lachnus), 103 kalnii (Lygus), 147 leta (Serenthia), 146 levigatus (Miris), 147 lanarius (Capsus), 216 lanternaria (Fulgoria), 182 lativentris (Nabis), 146 limbatus (Nabis), 146 lineatus (Nysius), 146 lineolatus (Calcoris), 147 littoralis (Salda), 147 lituratus (Piezodorus), 146 locustris (Gerris), 146 longipennis (Macrosiphum), 102 lonicerze (Rhopalosiphum), 103 loti (Macrosiphum), 101 luctuosus (Schirus), 146 maculatus (Corizus), 146 merkeli (Pithanus), 147 mesta (Corixa), 147 major (Nabis), 146 malvze (Macrosiphum), 101 marginatus (Syromastes), 146 melanocephalus (Hyalopterus), 103 melanocephalus (Phylus), 147 merioptera (Heterotoma), 147 micropterum (Macrodema), 146 minuta (Triphleps), 147 nasturtil (Aphis), 102 nemoralis (Anthocoris), 147 nemorum (Anthocoris), 147 nymphexe (Rhopalosiphum), 104 ochromelas (Calocoris), 147 ochrotrichus (Orthotylus), 147 padi (Aphis), 102 palliceps (Phylus), 147 pastinace (Lygus), 147 pastinacex (Siphocoryne), 103 paykulli (Macrotylus), 147 pedestris (Stygnus), 146 petasitidis (Aphis), 102 picere (Lachnus), 104 piceus (Drymus), 146 pilosella (Salda), 147 . pini (Aphanus), 146 polygoni (Aphis), 102 INDEX. xl populus (Chaitophorus), 103 pretextatus (Rhyparochromus), 146 prasina (Palomena), 146 primulz (Macrosiphum), 101 punctatus (Rhacognathus), 146 pyri (Myzus), 102 quercus (Psallus), 147 radicis (Trama), 104 *Rectinasus, 28 ranunculi (Aphis), 102 reuteri (Phytocoris), 147 rosarum (Myzus), 102 roseo-maculatus (Calocoris), 147 roseus (Psallus), 147 | rotunda (Forda), 30 rubiellum (Macrosiphum), 101 | rufipes (Pentatoma), 146 | rugosus (Nabis), 146 sahlbergi (Corixa), 147 salicis (Melanoxantherium), 104 saltatoria (Salda), 147 scapha (Knoplops), 146 scarabeoides (Thyreocoris), 146 signata (Lachnus), 103 sileneum (Macrosiphum), 102 Order XVI. alba (Chrysopha), 67 aleyrodiformis (Semidalis). 67 angulatus (Micromus), 67 arakave (Panorpa), 230 Ascalaphus, 279, 303 atrifrons (Hemerobius), 68, 209 Aulops, 229 beticus (Ascalaphus), 204 Bittacus, 229, 230 Boreus, 229 Boriomyia, 209 capitata (Nothochrysa), 68 coccajus (Ascalaphus), 97, 98 cognata (Panorpa), 43, 68, 179, 191 communis (Panorpa), 68, 191, 229 concinnus (Hemerobius), 190, 209 Coniopteryx, 134 conspersus (Sympherobius), 212 elegans (Hemerobius), 67, 209, 210, 211, 212 flava (Chrysopa), 46, 67, 191 fuliginosa (Sialis), 66 fuscata (Sisyra), 67 germanica (Panorpa), 68, 99, 19i hageni (Panorpa), 229 hakusanensis (Panorpa), 230 Hemerobius, 209 hispanicus (Ascalaphus), 204 humuli (Hemerobius), 67, 209 inconspicuus (Hemerobius), 68, 209, 210 klugi (Panorpa), 230 Leptopanorpa, 229 limbatellus (Hemerobius), 209 longicornis (Ascalaphus), 204 lutaria (Sialis), 66,98, 190 lutescens (Hemerobius), 67, 209 maculicollis (Raphidia), 190 stagnorum (Hydrometra), 146 staphylew (Rhopalosiphum), 103 stellarie (Macrosiphum), 101 subapterus (Coranus), 146 sylvaticus (Drymus), 146 sylvestris (Anthocoris), 216 taraxaci (Macrosiphum), 101 tenellus (Orthotylus), 147 thomsoni (Scolopostethus), 146 thoracica (Harpocera), 147 ticinensis (Calocoris), 147 tilie (Pediopsis), 229 tipularius (Neides), 146 tricornis (Dictyonota), 146 trifolii (Macrosiphum), 101 tripustulatus (Liocoris), 147 ulmi (Phytocoris), 147 urticee (Heterogaster), 146 variabilis (Psallus), 147 varians (Psallus), 147 verna (Campylostira), 146 veronice (Macrosiphum), 102 virgula (Campyloneura), 147° viridis (Chermes), 182 whitei (Myzus), 103 NEUROPTERA. marginatus (Bittacus), 230 marshami (Hemerobius), 211, 212 micans (Hemerobius), 67, 191, 209 mortoni (Hemerobius), 210 nervosus (Hemerobius), 67, 191, 209 nitidulus (Hemerobius), 67, 209 notata (Raphidia), 66, 98, 190 orientalis (Corydalis), 43 orotypus (Hemerobius), 67, 209 paganus (Micromus), 67 Panorpa, 43, 229, 230 Panorpodes, 229, 230 parvulus (Hemerobius), 209 pellucidus (Hemerobius), 210 perla (Chrysopa), 67, 98, 191 phyllochroma (Chrysopa), 67 pini (Hemerobius), 210 plumbeus (Creagris), 204 prasina (Chrysopa), 67 psociformis (Coniopteryx), 191 psociformis (Conwentzia), 67 pygmaeus (Hemerobius), 212 ’ quadrifasciatus (Hemerobius), 67, 99, 190, 209 septempunctata (Chrysopa), 67 stigma (Hemerobius), 68, 191, 209 striatellus (Sympherobius), 210, 211, 212 subnebulosus (Hemerobius), 67, 209, 212 Sympherobius, 209 takaoensis (Bittacus), 230 tenella (Chrysopa), 67, 191 tineiformis (Coniopteryx), 68 venosus (Sympherobius), 212 ventralis (Chrysopa), 67 vulgaris (Chrysopa), 68, 99, 191 xanthostigma (Raphidia), 67 Xl INDEX. Order XVII. TRICHOPTERA. albardana (Rhyacophila), 99 centralis (Limnophilus), 78 *chapmani (Metancea), 49, 50, 51, 99 fimbriata (Apatania), 99 flavipennis (Metancea), 49, 50, 51 granulatus (Plitocolepus), 98 latipennis (Stenophylax), 99 ludificatus (Philopotamus), 98 pedemontanum (Sericostoma), 99 pullata (Berwa), 99 ucenorum (Stenophylax), 99 Order XVIII. LEPIDOPTERA. *abannulata (Hrebia), 283 abbreviata (Eupithecia), 111, 120 aboculata (Hrebia), 283 abruptaria (Hemerophila), 227 absinthiata (Eupithecia), 110 acacie (Thecla), 16, 20, 56, 271 achatinella (Nyctegretes), 245 achiller (Anthrocera), 311 achillez (Zygena), 63 *acronyctoides (Stretchia), 163 actzon (Thymelicus), 20, 57, 59 acuminitana (Dichrorampha), 106 acuminitana (Hemimene), 106 adippe (Argynnis), 13, 19, 20, 128 adonis (Agriades), 17 adrasta (Pararge), 35 adusta (Hadena), 275 adustata (Ligdia), 110, 302 advena (Philosamia), 110, 111 adyte (Erebia), 34, 35 zegon (Lycena), 110, 150 segon (Plebeius), 10, 16, 57,177, 278, 282 gon (Rusticus), 61 aéllo (Gineis), 303 zstimaria (Semiothisa), 63 zetheria (Melita), 294 afer (Hrebia), 236, 296 agathina (Agrotis), 111, 123 aglaia (Argynnis), 19, 20, 45, 46, 57, 89, 128, 285, 312, 313 *albibasis (Macrobarasa), 220 *albibasis (Polyploca), 322 *albicosta (Hyposada), 168 *albidisca (Chytonix), 165 *albidorsalis (Asura), 161 *albigutta (Oruza), 167 *albipuncta (Mecodina), 222 *albirena (Euplexia), 165 albistriana (Peronea), 112 albistriga (Pydna), 323 albonota (Huplexia), 166 albonotata (Chytonix), 165 albula (Nola), 39 albulata (KEmmelesia), 275, 276 alezee (Carcharodus), 175, 177, 316 alcee (Erynnis), 20, 206 alcetas (Everes), 273 alchemillata (Perizoma), 254 alciphron (Chrysophanus), 13 alcon (Lycena), 127 alcyone (Satyrus), 13, 14, 17, 18, 20, 59 alecto (Hrebia), 282, 284, 309 alexandre (Ornithoptera), 46 alexanor (Papilio), 55 allionia (Tephroclystia), 62 alni (Jochera), 279, 298 alpina (Ithysia), 92 alpinellus (Crambus), 246 alpinum (Daseocheta), 183 alstromeriella (Depressaria), 259, 289 altheew (Carcharodus), 126, 313 althes (Spilothyrus), 155 alveus (Hesperia), 12, 13, 20, 57, 58, 313, 89, 126, 141, 177, 178, 285, 310, 312 amandus (Polyommatus), 241, 273 amata (Timandra), 302 amataria (Timandra), 54 amathusia (Brenthis), 56, 312, 313 Anacroniata, 183 ancilla (Naclia), 45 anderida (Heliconius), 107 andrei (Philosamia), 111 andromedx (Hesperia), 285, 286, 310, 312, 313 angelice (Zygena), 61, 63 angulifera (Samia), 279 angustalis (Cledeobia), 244 annulata (Ephyra), 43 annulata (Zonosoma), 43, 46 annulatus (Cordulegaster), 325 anthe (Satyrus), 297 Anthrocera, 303, 326 anthyllidis (Anthrocera), 326 antico-obsoleta (Polyommatus), 327 antiopa (Euvanessa), 20, 56, 277 antiopa (Vanessa), 301 antiqua (Orgyia), 225, 283 Apocheima, 92 apollo (Parnassius), 10, 11, 12, 13, 45, 57, 90, 110, 127, 229, 282, 311, 313 apollonius (Parnassius), 229 appendiculata (Brachodes), 318 arcania (Ccenonympha), 11, 14, 19, 20, 316 arenacearia (Eubolia), 318 arge (Melanargia), 134 argentina (Cucullia), 317 | argentipedella (Nepticula), 208 INDEX. argentula (Banksia), 299 argentula (Erastria), 317 argiades (Lycena), 179 argiolus (Celastrina), 13, 20, 46, 229, 293, 301 argiolus (Cyaniris), 110, 206, 229, 276, 301, 328 argus (Argina), 159 argus (Lycena), 110, 150 argus (Plebeius), 10, 12, 13, 16, 20, 57, 90, 127, 156, 177, 273, 282, 310, 313 argyrognomon (Plebeius), 56, 57, 59, 89, 127, 273 arion (Lycena), 10, 12, 13, 56, 57, 241, 293, 313 aristeus (Satyrus), 175, 177 *arizanensis (Thermesia), 320 armoricanus (Hesperia), 12, 142, 178, 316 arsilache (Brenthis), 128 artaxerxes (Lycena), 110 artemis (Melitea), 136 arundineta (Nonagria), 253 arundinis (Nonagria), 253 ashworthii (Agrotis), 110, 112, 328 aspersana (Peronea), 245 astrarche (Lycena), 18, 47, 70,106, 110, 328 astrarche (Plebeius), 39, 149 astrarche (Polyommatus), 155, 273 atalanta (Pyrameis), 13, 19, 35, 41, 70, 105, 150, 151, 174, 177, 181, 193, 226, 276, 284, 296, 301, 303, 313, 324 athalia (Melitea), 10, 16, 20, 134, 182, 207, 313 atomaria (Ematurga), 47, 110, 123, 206, 254, 318 atomaria (Fidonia), 135, 136, 208, 226 atricapitana (Eupeecilia), 247 atriplicis (Hadena), 298, 299, 314, 315 atropos (Acherontia), 205, 224, 227, 328 atropos (Manduca), 301 Audela, 183 augusta (Aporia), 154 aurantiaca (Papilio), 269 aurelia (Melitsea), 294 aurinia (Melitea), 45, 110, 128, 207 ausonia (Anthocharis), 270 ausonia (Kuchloé), 19, 133, 154, 155 australis (Acidalia), 62 australis (Aporophylla), 110 Automeris, 44 autonoé (Satyrus), 242 avellanella (Ornix), 208 aversa (Gonanticlea), 292 aversata (Acidalia), 62 *azurica (Polyommatus), 127 badiata (Anticlea), 227 baliodactyla (Aciptilia), 245 Baratha, 183 baroni (Melitzea), 195 barrettii (Diantheecia), 45, 327 basalis (Nanaguna), 169 xill | basijuncta (Polyommatus), 327 basilinea (Apamea), 227, 253 baton (Polyommatus), 154, 175, 177 baton (Scolitantides), 273 bavius (Scolitantides), 243 belia (Anthocharis), 270 bella (Hromene), 62, 63 bellargus (Agriades), 17 bellargus (Lycsena), 110 bellargus (Polyommatus), 274 bellidice (Pontia), 269, 270 bellieri (Hesperia), 58, 126, 142, 178 bellieri (Lycena), 151 bellieri (Polyommatus), 177 betule (Thecla), 120 betularia (Pachys), 254 betulella (Phycis), 260 biarcuata (Polyommatus), 327 bicolorana (Hylophila), 62, 63, 124 bicoloria (Miana), 302 bidentata (Gonodontis), 76, 132, 227, 290 *bifasciata (Thermesia), 320 bifida (Cerura), 277 *biformata (Phoenicoprocta), 54 bilineata (Camptogramma), 254 bilineata (Larentia), 62 bilunaria (Selenia), 47, 254, 302 binaria (Drepana), 62 *bipartita (Eustrotia), 168 *bipuncta (Cirphis), 164 bipunctanus (Melissoblaptes), 245 bipunctaria (Eubolia), 109 bipunctaria (Ortholitha), 245 bipupillata (Ceenonympha), 19 biselliella (Tinea), 77 Biston, 92 bistortata (Tephrosia), 110 biundularia (‘l'ephrosia), 109 beetica (Melitwea), 44 beeticus (Lampides), 149, 176, 177 boisduvali (Pseudacrea), 44 bractea (Plusia), 135 brassicz (Pieris), 13, 19, 128, 149, 151, 153, 158, 174, 175, 177, 206, 269, 313 breviculata (Tephroclystia), 62 brevilinea (Arenostola), 225 brevilinea (Leucania), 225 broadwayi (Napata), 54 brumata (Cheimatobia), 120, 123 brunnea (Noctua), 254 bryoniz (Pieris), 90, 313 bucephala (Phalera), 228, 253 cacaliz (Hesperia), 58, 126, 285, 286, 313 cecus (Hesperia), 178 *cerulea (Polyommatus), 277 cerulea-grisea (Cupido), 274 exruleocephala (Diloba), 111 ceruleopunctata (Chrysophanus), 20 cresia (Dianthecia), 111 cesiata (Larentia), 275 calabraria (Rhodostrophia), 62 e-album (Grapta), 325 c-album (Polygonia), 19, 56, 57, 155, 177, 206, 294, 528 Cc X1V calida (Polyommatus), 175, 177 caliginea (Anacroniata), 183 callidice (Pontia), 58, 285, 313 Callidryas, 204 calliopsis (Plebeius), 56 Calocasia, 183 Calymnia, 48 camelina (Lophopteryx), 228 camilla (Limenitis), 11, 17, 19, 56, 312, 313 candidata (Asthena), 110, 111 caniola (Lithosia), 63 canningi (Philosamia), 111 cantaneri (Thais), 43 capsincola (Dianthecia), 228, 229, 253, 254 eapsophila (Dianthecia), 45, 111, 328 cardamines (Euchloé), 10, 13, 47, 133, 154, 180, 181, 206, 207, 225, 251, 270, 301, 313, 327 cardui (Pyrameis), 10, 13, 17, 19, 41, 70, 128, 149, 155, 173, 176, 177, 276, 278, 284, 294, 301, 303, 313, 324 carlin (Hesperia), 142, 178, 286, 310, 312, 313 carlota (Phyciodes), 194, 195 carniolica (Anthrocera), 59, 311 carpini (Saturnia), 104 carpophaga (Diantheecia), 228, 253 carthami (Hesperia), 20, 57, 89, 126 cassinea (Bombyx), 122 cassioides (Hrebia), 57, 59, 129, 284 cassiope (Hrebia), 57, 90, 128, 282, 308, 309, 313 casta (Calophasia), 317 castrensis (Malacosoma), 317 Catephia, 183 Cauninda, 183 celerio (Chzerocampa), 40, 135 celerio (Hypotion), 40 celtis (Libythea), 18, 20, 236, 293 centumnotata (Cidaria), 48, 328 cerri (Thecla), 15 cespitalis (Herbula), 244 cespitis (Luperina), 45 cespitis (Tholera), 302, 303 ceto (Erebia), 108, 128, 282, 308, 313 chamomille (Cucullia), 110 chi (Polia), 328 chlorana (Earias), 40 chloridice (Pontia), 242 christiienssoni (Colias), 271 chrysidiformis (Sesia), 260 chrysitis (Plusia), 131, 254 chryson (Plusia), 131 cinerea (Agrotis), 227, 253 cinnus (Agriades), 18, 20 cinxia (Melitewa), 19, 46, 294 circe (Hipparchia), 156 circe (Satyrus), 20, 59, 176, 177, 296 circellata (Acidalia), 208, 226 circuitaria (Acidalia), 62 cirsii (Hesperia), 57, 126, 142, 177, 178 cleodoxa (Argynnis), 155 clathralis (Phlyctenodes), 318 INDEX. cleopatra (Gonepteryx), 16, 19, 107, 157 clerkella (Lyonetia), 157 clymene (Pararge), 241, 315 clytie (Apatura), 279 e-nigrum (Noctua), 302 Coatlantona, 134 celata (Pseudomicronia), 202 celestina (Glaucopsyche), 240, 274 ceelibaria (Gnophos), 38 ccenia (Junonia), 193 ceenia (Lithacodia), 168 coenosa (Lelia), 315 ceruleopunctata (Chrysophanus), 301 coerulescens (Polyommatus), 286 Colias, 271 combusta (Xylophasia), 135 comes (Triphzena), 303 comma (Augiades), 313 comma (Hesperia), 156 comma (I.eucania), 228, 253 complana (Lithosia), 63 compta (Dianthecia), 62 concinnata (Cidaria), 47 concolor (Tapinostola), 46 conflua (Noctua), 275 confluens (Parnassius), 111 coniferana (Stigmonota), 247 conigera (Leucania), 254, 302 *conjuncta (Trachea), 29 *connexa (Laphygma), 166 consobrina (Zygeena), 63 consortaria (Boarmia), 318 *conspecta (Hriopyga), 163 *conspersa (Bapta), 201 conspersa (Dianthcecia), 110, 275, 276 contaminei (Anthrocera), 326 contaminellus (Crambus), 244 *contigua (Fodina), 221 contiguaria (Acidalia), 111, 328 conversa (Catocala), 62 conversaria (Boarmia), 46, 48, 327 convolvuli (Sphinx), 72, 324 conyze (Hesperia), 178 cordula (Satyrus), 10, 11, 13, 14, 56, 312 corinna (Cenonympha), 150, 151, 174, 175, 177 coronana (Peronea), 112 corsica (Lycena), 151 corsica (Orgyia), 150, 151, 177 *cortes (Napata), 54 corticea (Agrotis), 254 corydon (Agriades), 11, 13, 18, 20, 46, 127 corydon (Lycena), 110, 251 corydon (Polyommatus), 311, 313 coryli (Demas), 183 Cosmia, 48 Cosmodesmus, 107 cossoides (Batracharta), 221 costalis (Pyralis), 131 costajuncta (Polyommatus), 327 costana (Tortrix), 135 crabroniformis (Trochilium), 135 INDEX. XV Crambus, 61 crategi (Aporia), 10, 13, 19, 153, 154, 269, 282, 296, 311, 313 craterellus (Crambus), 61, 63 crepuscularia (Tephrosia), 109, 227 cribrellum (Hesperia), 8, 316 cribrum (Emydia), 160, 245 cribrum (Myelois), 204 cribrum (Myelophila), 204 croatica (Macroglossa), 317 crocale (Callidryas), 204 crocale (Catopsilia), 204 crocealis (Ebulea), 259 cruciferarum (Plutella), 205, 225 cruda (Txniocampa), 227 cucubali (Diantheecia), 72, 111, 227, 253, 254 cuculatella (Nola), 120, 123, 124, 135 culiciformis (Sesia), 260 culmellus (Crambus), 61, 63 cuneata (Abraxas), 136 Curetis, 181 cyllarus (Glaucopsyche), 45, 293 cyllarus (Nomiades), 11 cynthia (Melita), 128 cynthia (Philosamia), 279 damon (Agriades), 127 damon (Polyommatus), 89, 286, 313 damone (Euchloé), 133, 134, 154 daphne (Brenthis), 295 daplidice (Pieris), 154, 155 daplidice (Pontia), 175, 177, 269 dardanus (Papilio), 44 darwiniana (Ccenonympha), 57, 128 Daseocheta, 183 dealbata (Scoria), 318 decipiens (Kerala), 220 decorata (Acidalia), 61, 62 defoliaria (Hybernia), 135 degeneraria (Acidalia), 62 deione (Melita), 286 Delias, 280 delius (Parnassius), 57, 89, 111, 127, 310, 312, 313 delphius (Parnassius), 229 dentalis (Odontia), 245 dentina (Mamestra), 110, 227, 253 deplana (Lithosia), 47 *derufata (Melitea), 56 desfontainii (Melitea), 44, 46 designata (Coremia), 302 determinata (Acidalia), 60, 61, 62 dia (Brenthis), 16, 19, 20, 295, 313 diana (Colias), 271 dichotoma (Amata), 319 dicta (Pheosia), 227 dictynna (Melitsza), 10, 313 didyma (Melitswa), 19, 20, 46, 56, 134, 313 dilucida (Apopestes), 62 dilucidana (Conchylis), 245 dilutaria (Acidalia), 62 dilutata (Oporabia), 111 Diphthera, 183 diplaga (Euproctis), 322 dipsaceus (Heliothis), 317 discobolus (Parnassius), 229 *discitincta (Cosmotriche), 321 Dismorpha, 280 dispar (Lymantria), 111 disseverans (Baratha), 183 distributa (Nola), 161 *divisa (Batracharta), 221 divisana (Peronea), 112 dolus (Polyommatus), 18, 20 dominula (Callimorpha), 72 donzelii (Polyommatus), 286, 313 dorilis (Chrysophanus), 10, 13, 272 doris (Heliconius), 44 dorus (Ccenonympha), 19, 20 doubledayaria (Pachys), 204 dromus (Hrebia), 57, 284 *dubia (Semiothisa), 291 dubitata (Triphosa), 254 duponcheli (Hrebia), 58, 59, 128, 129, 283, 313 dysodea (Hecatera), 277 edusa (Colias), 13, 19, 40, 41, 42, 46, 47, 59, 70, 90, 128, 149, 155, 158, 174, 175, 176, 177, 206, 207, 270, 271, 278, 300, 301, 303, 313 egea (Vanessa), 133, 155 egeria (Pararge), 70, 106, 131, 149, 174, 177, 207 egerides (Pararge), 35, 316 egialea (Amauris), 107 eleus (Chrysophanus), 20, 149, 151,173, 177 elinguaria (Crocalis), 132, 254, 302 elisa (Argynnis), 173, 174, 176, 177 elongella (Gracilaria), 259 emutaria (Acidalia), 324 eos (Melitza), 182 epiphron (Erebia), 91, 128, 309 Erebia, 34, 91 eremita (Psilura), 46 eris (Argynnis), 19, 20, 46, 57, 89, 156, 295, 313 eroides (Polyommatus), 273 eros (Polyommatus), 57, 127, 273, 286, 309, 313 erynnys (Erebia), 129 erythrus (Zygeena), 62, 63 escheri (Agriades), 13, 57, 59, 127 escheri (Polyommatus), 17, 20, 158, 286, 313 esculi (Thecla), 16, 20 Euclidia, 183 Euclidimera, 183 eumedon (Aricia), 303 eumedon (Polyommatus), 285, 313 eupheme (Zegris), 236, 240, 270 euphenoides (Euchloé), 132 euphorbie (Deilephila), 62, 224 euphorbie (Hyles), 224 euphborbiata (Minoa), 62 euphrosyne (Argynnis), 207 euphrosyne (Brenthis), 10, 20, 47, 295, 313 XV1 Kupithecia, 71 euryades (Heliconius), 158 euryale (Erebia), 57, 129, 282, 286, 312, 313 eurybia (Chrysophanus), 57, 89, 127, 285, 310, 313 eurytheme (Colias), 193 exalbata (Siona), 318 exclamationis (Agrotis), 228, 253, 254 exigua (Caradrina), 62 extrema (Zizera), 327 exulans (Anthrocera), 286, 310 exulans (Zygena), 180 exulis (Crymodes), 275 fabricana (Sericoris), 76 fagella (Chimabacche), 260 falcataria (Drepana), 110 fascelina (Dasychira), 159 fascelis (Melitea), 295 *fasciata (Pseudomicronia), 201 fausta (Anthrocera), 59, 311 favicolor (Leucania), 277 favillaceana (Capua), 47 ferrugata (Coremia), 110, 227, 254, 302 festuce (Phytometra), 183 ficklini (Dianthecia), 43 filigrammaria (Oporabia), 111 filipendulw (Anthrocera), 158, 326 filipendule (Zygrna), 63, 160, 300 fimbria (Agrotis), 122 fimbria (Triphena), 122, 125 flammea (Meliana), 253 flava (Adopza), 317 flavipalliata (Abraxas), 136 flavicincta (Polia), 39, 302 flavus (Thymelicus), 10, 13, 20 fluctuata (Xanthorhoé), 227, 253, 302, 303 fluviata (Percnoptilota), 38, 111 formicipennis (Sesia), 260 *formosana (Liparopsis), 323 formosa (Kuchromia), 159 foulquieri (Hesperia), 58, 126, 178 foulquieri (Polyommatus), 17 franconica (Clisiocampa), 133 fraxinata (Kupithecia), 110, 135 fraxini (Catocala), 40, 135 frithi (Antherea), 111 fritillum (Hesperia), 57, 58,126,177, 178 frugalis (Pydna), 267 frugalis (Remigia), 183 fuciformis (Hemaris), 62 fugax (Solenopsis), 43 fulgurita (Kribomorpha), 279 fulvago (Xanthia), 303 fulvana (Catoptria), 245 fulvata (Larentia), 62 fumaria (Biston), 181 fumata (Acidalia), 47, 110 funebris (Pyrausta), 63 furcata (Hydriomena), 254 furva (Mamestra), 275, 328 *fusca (Fodina), 221 *fuscimarginalis (Nola), 161 INDEX. gabrielis (Papilio), 181 galatea (Melanargia), 11, 12, 14, 155, 156, 296, 313 galiata (Xanthorhoé), 323 gallii (Celerio), 228, 279 gambrisius (Papilio), 181 gamma (Plusia), 41, 111, 131, 135, 228, 253, 254, 302, 303, 317 gavarnica (Hrebia), 283 gemmaria (Boarmia), 254 gemmiferana (Laspeyresia), 328 genistea (Mamestra), 227 gentiana (Penthina), 328 geryon (Adscita), 107 geryon (Ino), 107 gigantea (Conchylis), 245, 297 gilvago (Mellinia), 47 gilvaria (Aspilates), 246 glabra (Orrhodia), 106 glacialis (Krebia), 128 glareosa (Noctua), 276 glariaria (Phasiane), 318 glauca (Hadena), 47 glauca (Mamestra), 110 glaucata (Cilix), 120, 254 glaucinaria (Gnophos), 228 glaucopsis (Ceenonympha), 19 globularis (Ino), 63 globulariz (Procris), 317 glyphica (Euclidia), 62 goante (Hrebia), 57, 90, 129, 313 Gonospileia, 183 gordius (Chrysophanus), 13, 15, 20, 59 gordius (Lycena), 154 gorge (Hrebia), 58, 90, 91, 129, 284, 285, 313 gorgone (Erebia), 90 gorgophone (Erebia), 90, 91, 128 gothica (Tzniocampa), 227 gracilis (Teniocampa), 76, 111, 227 greecaria (Ithysia), 92 graminis (Chareas), 38, 276 egriseata (Lithostege), 71 *griseotincta (Albara), 267 grossulariata (Abraxas), 105, 106, 107, 109, 136, 328 gutta (Plusia), 317 gyrata (Ephyra), 62 halterate (Diptilon), 135 hamana (Euxanthis), 318 *hampsoni (Metzmene), 319 hardwickii (Parnassius), 229 hartmanniana (Argyrolepia), 47 hastiana (Peronea), 77, 111 haworthii (Celena), 276 hecate (Brenthis), 16, 19, 20 hecatzus (Papilio), 46 hecla (Colias), 82, 83, 84, 85, 270 hecuba (Ornithoptera), 46 helice (Colias), 158, 176, 207, 327 Heliconius, 47 helvola (Lithosia), 47 herbosana (Dichrorhampha), 106 herbosana (Hemimene), 106 INDEX. hermione (Hipparchia), 156 hermione (Satyrus), 11, 14, 19, 20, 296 herrichi (Parnassius), 111 Hesperia, 177 hesperica (Plebeius), 44, 45 hiera (Pararge), 10, 15 hippocrepidis (Anthrocera), 326 hippolyte (Satyrus), 242 hippothoé (Chrysophanus), 310 hirtaria (Biston), 71, 180 hirtaria (Lycia), 92, 93, 94, 327 hispana (Agriades), 180 hispana (Polyommatus), 180 hispidaria (Apocheima), 207 hispulla (Epinephele), 149, 173, 176, 177 hobleyi (Pseudacreea), 44 hospita (Parasemia), 285 hospiton (Papilio), 148, 176, 224 humili (Hepialus), 275 hutchinsoni (Grapta), 325 hutchinsoni (Polygonia), 294, 328 hyale (Colias), 12, 13, 19, 59, 90, 177, 206, 207, 270, 271, 313 hydara (Heliconius), 158 hylas (Agriades), 127 hylas (Polyommatus), 12, 13, 20, 57, 282, 286, 310, 311,313 hyperanthus (Aphantopus), 11, 14, 45 iacularia (Rhodostrophia), 318 iberica (Melitea), 46 icarinus (Polyommatus), 16, 46 icarus (Lycena), 41, 70, 106 icarus (Polyommatus), 10, 13, 17, 20, 39, 46, 127, 149, 153, 158, 173, 174, 175, 177, 207, 212, 228, 251, 273, 277, 278, 279, 280, 303, 309, 313, 327, 328 ichnusa (Aglais), 150, 174, 177 ictericana (Spaleroptera), 244 ida (Epinephele), 149, 175, 176, 177 ilia (Apatura), 279 iliades (Apatura), 279 ilicifolia (Gastropacha), 158, 228, 327 ilicifolia (Lasiocampa), 157 ilicis (Thecla), 11, 13, 16, 20, 27, 312, 313 illunaris (Pseudophia), 62 illustris (Automeris), 279 imitata (Acidalia), 62 immaculata (Dryas), 175, 176, 177 immaculata (Scolitantides), 273 imperator (Parnassius), 229 impura (Leucania), 254, 303 inequalis (Agriades), 327 incarnata (Heliothis), 317 inconspicua (Pydna), 267 indica (Pyrameis), 43 indica (Vanessa), 43 infausta (Aglaope), 56 ino (Brenthis), 285, 311, 312, 313 inornata (Acidalia), 62 inquinatellus (Crambus), 247 instabilis (Teniocampa), 227 insularis (Antherea), 111 intermedia (Epinephele), 316 XVll intermedia (Mellinia), 47 intermedia (Pararge), 20 intermedia (Polyommatus), 18 io (Vanessa), 13, 41, 70, 174, 177, 205, 207, 276, 324 iochalcea (Abraxas), 136 iphioides (Coenonympha), 316 iphis (Cononympha), 57, 89, 128, 310, 313 iris (Apatura), 279 *isabelle (Pecilopsis), 92, 93, 94 ismeria (Phyciodes), 194, 195 isomera (Eustrotia), 169 italica (Ithysia), 92 Ithysia, 92 jacobee (Hypocrita), 180, 227, 253 jaguarinaria (Arichanna), 202 japygia (Melanargia), 156 jasius (Charaxes), 133, 177 jucunda (Kublemma), 63 jurtina (Epinephele), 14, 20, 47, 128, 149, 206, 232, 313, 315 *kanshireiensis (Pydna), 322 *kanshireiensis (Thermesia), 320 *kanshireiensis (Semiothisa), 290 kuhlmanni (Argynnis), 295 lacinia (Synchloé), 195 lacticolor (Abraxas), 136, 328 lacunana (Sericoris), 76 lanarius (Microbiston), 92 lanceolata (Ceenonympha), 226 lanestris (Kriogaster), 134, 152, 157 lappona (Hrebia), 129, 285, 286, 312, 313 lapponaria (Peecilopsis), 92, 93, 94 lariciaria (Boarmia), 39 lastoursi (Philosamia), 111 lathonia (Issoria), 13, 59, 89, 128, 129, 149, 174, 177, 295, 313 lavandule (Zygena), 61, 63 lavatere (Carcharodus), 313 leander (Ceenonympha), 241, 316 lecheana (Ptycholoma), 158 . lefebvrei (Hrebia), 284 *lentiginosa (Kerala), 220 leonardi (Parnassius), 111 leporina (Acronycta), 110 leucomelanella (Lita), 208 leucophearia (Hybernia), 120, 183 levana (Araschnia), 325 libythea (Appias), 44 licheana (Tortrix), 259 lichenea (Epunda), 135 ligea (Hrebia), 34, 35 ligustri (Craniophora), 164 lilacina (Dryas), 182 limbatus (Teracolus), 44 Limenitis, 232 limitata (Ortholitha), 254 lineago (Mellinia), 47 linearia (Ephyra), 62, 303 lineola (Adopea), 41, 311, 312, 317 lineola (Thymelicus), 13, 20, 57, 126 literosa (Miana), 111 lithargyria (Leucania). 110, 254, 802 XVill lithoxylea (Xylophasia), 254 litigiosaria (Acidalia), 61, 62 littoralis (Leucania), 111, 225 littoralis (Prodenia), 157 liturata (Semiothisa), 76, 110 lobulina (Cosmotriche), 321 lonicere (Anthrocera), 286, 311 lonicerse (Zygzena), 61, 63 lubricipeda (Spilosoma), 253 lucernea (Agrotis), 47, 110, 135, 328 lucida (Acontia), 317 lucilla (Neptis), 241, 293 lucina (Nemeobius), 300 luctuosa (Acontia), 254 lunaria (Selenia), 279 lunigera (Agrotis), 328 lunosa (Anchocelis), 303 lunosa (Omphalocelis), 303 lupulina (Hepialus), 228 lurideola (Lithosia), 63, 254 lutea (Xanthia), 303 lutearia (Lythria), 318 luteata (Rumia), 62 luteolata (Opistograptis), 227, 253, 254, 302 lutulenta (Epunda), 105 lyeaon (Epinephele), 56, 89, 128, 313, 316 lychnidis (Amathes), 136, 303 lychnidis (Orthosia), 136 Lycia, 92 lycidas (Plebeius), 44 lydia (Polyommatus), 274 lyllus (Coenonympha), 173, 177 machaon (Papilio), 10, 13, 19, 127, 155, 175, 177, 187, 207, 253, 269, 282, 301, 311, 313 macilentaria (Acidalia), 61, 62 maculata (Agriades), 127 maculata (Perenia), 202 maculipennis (Plutella), 205, 225, 318 meniata (Ortholitha), 62 mera (Pararge), 10, 13, 20, 313, 316 magdalena (Melitsea), 19 magnifica (Citheronia), 279 magnifica (Parnassius), 110 malvz (Hesperia), 142, 178, 317 malvoides (Hesperia), 58, 142, 178, 285, 313 manni (Pieris), 269 margaritellus (Crambus), 226 marginaria (Hybernia), 135 *marginata (Bapta), 201 marginata (Ligdia), 228, 254 marginata (Lomaspilis), 302 marginepunctata (Acidalia), 62, 108, 318 maritima (Senta), 299 marmorinaria (Hybernia), 183 matura (Cerigo), 254, 302 maura (Mania), 280 mayrana (Peronea), 112 medon (Aricia), 12, 13, 16, 18, 20 medon (Plebeius), 39, 106 medon (Polyommatus), 127, 310, 313 INDEX. megera (Pararge), 11, 13, 20, 41, 70, 206, 207, 313, 316 melampus (Erebia), 309, 313 Melanargia, 46 melanella (Lita), 159° melanotoxa (Polyommatus), 327 meleager (Polyommatus), 18 Melinza, 47 Melitwa, 134 melotis (Hesperia), 178 mendica (Diaphora), 110, 227 menephron (Psilogramma), 279 menthastri (Spilosoma), 110, 227, 253 menyanthidis (Acronycta), 40, 110 merope (Melita), 128, 310, 313 Metaporia, 280 meticulosa (Phlogophora), 254, 275, 302, 303 meticulosa (Trigonophora), 254 mi (Iuclidia), 110 mi (Euclidimera), 183 micacea (Hydreecia), 302, 303 microdactylus (Leioptilus), 328 mima (Hypolimnas), 158 miniata (Calligenia), 47 minima enaee 327 minimus (Cupido), 11, 13, 18, 20, 127, 207, 313 minutissimus (Agriades), 327 miniosa (Tsniocampa), 76 misella (Tinea), 318 mnemosyne (Parnassius), 241, 269 mnestra (Erebia), 58, 90, 91, 128, 284, 313 Mocis, 183 meeschleril(Hesperia), 316 Monacha, 136 monacha (Lymantria), 71, 251 monacha (Psilura), 46 monocharia (Phigalia), 135 moneta (Plusia), 160, 223 moniliata (Acidalia), 62 monoglypha (Xylophasia), 135, 254, 302 montanata (Xanthorhoé), 47, 228, 253, 275 morpheus (Caradrina), 253, 254, 303 mosara (Aidia), 222 mouffetella (Gelechia), 259 mucidaria (Gnophos), 63 mundana (Nudaria), 39 mundataria (Aspilates), 318 munita (Gonospileia), 183 munitata (Coremia), 275, 276 muricata (Hyria), 47 . murinaria (Kubolia), 63, 318 murinata (Minoa), 52 musculana (Cnephasia), 47 myrmidone (Colias), 206, 207 myrtilli (Anarta), 123 nana (Diantheecia), 72, 328 nanata (Eupithecia), 120 nanatella (Depressaria), 259 | napa (Brenthis), 128 INDEX. napi (Pieris), 10, 13, 19, 41, 136, 174, 177, 206, 303, 313 nebulosa (Aplecta), 45, 111, 124, 135, 328 nebulosa (Mamestra), 124 *nebulosa (Parasiccia), 162 *nebulosa (Pydna), 267 neera (Melita), 295 neglecta (Noctua), 111 neomiris (Satyrus), 174, 175, 176, 177 neril (Cherocampa), 40, 72 nerii (Daphnis), 40 neustria (Malacosoma), 62, 254 ni (Plusia), 317 niavius (Amauris), 107 nictitans (Hydreecia), 254, 302 nigra (Amporophyla), 303 nigra (Boarmia), 135 nigra (Odontoptera), 136, 328 nigrifoldella (Tinea), 232 *nigrifrons (Amata), 318 nigrofasciaria (Anticlea), 227 nigromaculana (Grapholitha), 245 *nigropunctata (Scolitantides), 273 nigrosparsata (Abraxas), 47, 328 niobe (Argynnis), 128, 295, 310, 312, 313 noctuella (Nomophila), 41 nymphagoga (Catocala), 62 obelisca (Agrotis), 110 obeliscata (Thera), 72, 111, 120, 231 oberthiiri (Philosamia), 111 oblongata (Eupithecia), 228, 253, 302 oblongata (Tephroclystia), 62 *obscura (Aidia), 222 obscura (Erebia), 108 obscura (Harmatelia), 222 obscura (Lycena), 293 *obscura (Westermannia), 169 *obscurata (Gnophos), 111 obscuraria (Acacis), 292 obsoleta (Leucania), 300 obsoleta (Zizera), 327 occidentalis (Hesperia), 178 occulta (Kurois), 275, 323 ocellaris (Mellinia), 47, 108 ocellata (Mesoleuca), 228, 254, 302 ocellatus (Smerinthus), 46, 251, 253, 327 ochracea (Ochria), 303 ochrata (Acidalia), 62, 244 “ochreipuncta (Micromonodes), 166 ochroleuca (Eremobia), 246 ochsenheimeri (Zygzena), 63 octogesima (Cymatophora), 300 octomaculalis (Ennychia), 259 octomaculata (Pyrausta), 63 ocularis (Acronycta), 298 ocularis (Palimpsestes), 314 oleracea (Mamestra), 254 *olivacea (Chytonix), 165 *olivescens (Heterolocha), 291 omphale (Chrysophanus), 272 ononaria (Aplasta), 62 X1X ononidis (Zygena), 63 onopordi (Hesperia), 141, 178 oo (Dicycla), 300 opalescens (Albara), 268 opalescens (Thyatira), 268 opima (Teniocampa), 227, 300 optilete (Polyommatus), 90, 127 orbifer (Pyrgus), 236, 316 orbicularis (Polyploca), 322 orbitulus (Plebeius), 57 orbitulus (Polyommatus), 127, 310, 313 orichalcia (Plusia), 131 ormenus (Papilio), 181 ornata (Acidalia), 302 ornata (Polyommatus), 16 ornithopus (Graptolitha), 25 ornithopus (Xylina), 125, 260 ostrina (Thalpochares), 43 palwno (Colias), 90 pales (Brenthis), 37, 128, 285, 312, 313 pallens (Leucania), 109, 111, 254, 255, 302 pallescens (Apatura), 279 pallescentella (Tinea), 232 pallida (Colias), 19, 270 pallida (Pydna), 267 *pallida (Rivula), 266 palpina (Pterostoma), 302 palumbella (Salebria), 63 palustris (Anthrocera), 326 pamphilus (Ccenonympha), 11, 14, 19, 20, 41, 70, 128, 206, 228, 231, 313, 316 pandora (Argynnis), 156 pandora (Dryas), 173, 174, 182, 175, 177 paniscus (Carterocephalus), 328 panoptes (Scolitantides), 273 Panthea, 183 , paphia (Antherwa), 279 paphia (Argynnis), 46, 70 paphia (Dryas), 19, 20, 148, 175, 176, 177 papilionaria (Geometra), 47, 109, 111, 122 parallela (Micra), 317 parisiensis (Agriades), 327 parthenias (Brephos), 47 parthenie (Melita), 17, 20 parvipuncta (Cyaniris), 174, 176, 177 pasiphaé (Epinephele), 20 pastinum (Toxocampa), 325 passetii (Hurois), 323 paula (Micra), 317 paupercula (Dryas), 175, 177 pavonia (Saturnia), 46, 104, 158 pedaria (Phigalia), 135 Pelamia, 183 pelopia (Argynnis), 46 peltigera (Heliothis), 111, 317 pendularia (Zonosoma), 43, 46 penella (Heterogynnis), 63 *pennata (Thyatira), 268 perfumaria (Boarmia), 48 XX perfusca (Notodonta), 72 Perisamia, 46 ’ perla (Bryophila), 302 perneyi (Antherea), 279 persona (Callimorpha), 46 petraria (Lozogramma), 228 pfluemeri (Syntomis), 45 pheodactylus (Mimacocoptilus), 245 Pharmacophagus, 107 pharte (EKrebia), 282, 286, 308, 309, 313 phasaianoides (Pelamia), 183 phegea (Syntomis), 45, 279, 303, 317 pheretes (Albulina), 303 pheretes (Polyommatus), 57, 90, 127, 309, 313 pherusa (Melanargia), 154, 229 phicomone (Colias), 12, 13, 57, 58, 59, 90, 128, 285, 311, 313 phleas (Chrysophanus), 15, 20, 41, 70, 127, 252, 272, 276, 301, 313 phleas (Rumicia), 327 pheebe (Melita), 20, 46, 311, 313 phryne (Triphysa), 242 Phyciodes, 134 Phytometra, 183 *picata (Craniophora), 164 Pieris, 44 pinetellus (Crambus), 247 piniperda (Panolis), 76 pisi (Mamestra), 228 plagiata (Anaitis), 228, 253 plantaginis (Nemeophila), 72, 107 plantaginis (Parasemia), 110, 285 Platycerusa, 183 plecta (Noctua), 302 plexippus (Anosia), 134 Plumigera, 136 Plusia, 183 pluto (Hrebia), 58, 128, 283 podalirius (Papilio), 11, 13, 19, 155, 177, 207, 269, 282, 313 Pecilopsis, 92 polemusa (Cirphis), 164 polonus (Agriades), 17, 20 polychloros (Eugonia), 11, 13, 19, 175, 177, 294 polygramma (Thalpochares), 62 polyphenaria (Dindica), 293 polyxena (Thais), 136, 154 pomonaria (Peecilopsis), 92, 93, 94 popularis (Epineuronia), 303 populeti (Txniocampa), 288, 300 populi (Amorpha), 46, 251, 327 populi (Pecilocampa), 120 populi (Smerinthus), 254, 327 porphyria (Agrotis), 275 *postflava (Arichanna), 282 postico-apicalis (Polyommatus), 327 postimaculata (Fodina), 221 *postvittata (Lithacodia), 168 *primula (Brenthis), 128 primule (Noctua), 254 procida (Melanargia), 20, 156, 296 INDEX. Prodromaria, 38 promethea (Samia), 279 pronoé (Hrebia), 159 pronuba (Triphena), 122, 125, 254, 275, 302, 303 pronubana (Tortrix), 76 protea (Eumichtis), 302 proto (Pyrgus), 316 prunaria (Angeronia), 47 pruni (Adscita), 56 pruni (Strymon), 207 pruni (Thecla), 271 pryadvena (Philosamia), 110 pryeri (Philosamia), 111 pseudonomion (Parnassius), 45 pulchella (Deiopeia), 160 pulchellata (Eupithecia), 228 *pulchra (Prionia), 291 pulchrina (Plusia), 254 pulverulenta (Te#niocampa), 76 pulveraria (Numeria), 110, 327 pumilata (Tephroclystia), 62 puncta (Agriades), 17 puncta (Polyommatus), 274 *punctivena (Archanara), 167 punctularia (Tephrosia), 111 pupillaria (Kphyra), 62 purpuralis (Anthrocera), 286 purpuralis (Pyrausta), 63 purpuraria (Lythria), 205, 318 *purpureofasciata (Huproctis), 321 purpurina (Micra), 317 purpurina (Thalpochares), 62 pygmeata (Hupithecia), 228 pygmeola (Lithosia), 244 pylaon (Scolitantides), 240, 273 pyraliata (Cidaria), 254 pyramidea (Amphipyra), 71, 280 pyrenella (Oreopsyche), 279, 280 pyri (Saturnia), 279 pyrina (Zeuzera), 254 pyropella (Pleurota), 318 quadrifasciaria (Coremia), 45 *quadrilinealis (Adrapsa), 222 quadripunctata (Caradrina), 254 quercana (Phibalocera), 120, 260 quercifolia (Gastropacha), 324 quercinaria (Hnnomos) 47, 120 quercus (Lasiocampa), 110, 111, 133, 324 quercus (Thecla), 120 quercus (Zephyrus), 20, 272 rachel# (Pecilopsis), 92, 93 radiata (Abraxas), 136 radiatella (Cerostoma), 119, 120 rape@ (Pieris), 13, 19, 41, 128, 132, 153, 175, 177, 193, 206, 269 raschkiella (Laverna), 208 ravida (Agrotis), 299, 318 Remigia, 183 renalis (Hoemerosia), 62 repandata (Boarmia), 46, 47, 109, 110, 111, 135, 288, 290, 327, 328 reticulata (Cidaria), 136 INDEX. XX1 reticulata (Neuria), 253, 279 rhamnata (Scotosia), 318 rhamni (Gonepteryx), 11, 13, 19, 177, 271, 280, 313 ribeana (Tortrix), 259 roboris (Lxosopis), 16, 20 robsoni (Aplecta), 47, 110, 111, 328 romanovi (Parnassius), 229 rosearia (Prionia), 292 rothliebii (Cenonympha), 47 rubi (Callophrys), 20, 186, 272 rubi (Macrothylacia), 123 rubi (Noctua), 253, 302 rubiginata (Acidalia), 62 rufa (Coenobia), 300 rufaria (Acidalia), 62 rufolunulata (Agriades), 45 rumicis (Acronycta), 62 rumina (Thais), 43 russata (Cidaria), 328 rutilus (Chrysophanus), 186, 187, 272 ryffelensis (Hesperia), 126, 178 sacraria (Sterrha), 62 Safia, 183 sagittata (Cidaria), 253, 314 sanguinalis (Pyrausta), 63 sao (Hesperia), 155, 312, 313 sao (Pyrgus), 20, 89, 126, 285 sareptana (Melitea), 294 sareptensis (Colias), 271 saturnana (Dichrorampha), 328 satyrion (Ccenonympha), 313 sarpedon (Anthrocera), 326 sarpedon (Zygeena), 63 scandanavica (Parnassius), 110 *schamyl (Callophrys), 272 schreibersiana (Commophila), 314 schmidtii (Chrysophanus), 277 scipio (Erebia), 55, 59, 128, 281, 310, 311, 312, 313 scirpi (Leucania), 62 scitula (Thalpochares), 62 scolieformis (Aigeria), 45 scripturosa (Xylina), 318 scutosa (Heliothis), 317 sebrus (Cupido), 274, 313 secalis eee 254, 302 segetum (Agrotis,) 253, 254 selene (Argynnis), 113 semele (Hipparchia), 20, 56, 315 semele (Satyrus), 70, 136 semi-allous (Lycena), 328 semiargus (Cyaniris), 329 semiargus (Lycena), 156 semiargus (Nomiades), 18, 20, 127, 282, 313 semisyngrapha (Agriades), 17, 46, 327 semisyngrapha (Lycena), 110 sepiaria (Trephonia), 62, 63 sequella (Cerostoma), 39 serena (Hecatera), 47, 254 sericea (Trisuloides), 183 sericealis (Rivula), 62, 266 sericeata (Acidalia), 61, 62, 318 serratule (Hesperia), 57, 58, 126, 141, 174, 177, 178, 285, 309, 312, 313 side (Hesperia), 317 silaceata (Hustroma), 111, 254 similata (Acidalia), 318 simplonia (Anthocharis), 58, 270, 282, 303, 308, 310, 312, 313 sinapis (Leptidia). 13, 19, 149, 150, 174 sinapis (Leptosia), 174, 177, 270, 313 sinapis (Leucophasia), 133, 206, 328 *sinuata (Eugoa), 161 smaragdaria, (Euchloris), 318 sobrinata (Eupithecia), 110 sodorensium (Boarmia), 46 solieraria (Boarmia), 62, 63 sordida (Hama), 253 *sordida (Nanaguna), 169 *sordida (Pydna), 267 spartiata (Chesias), 110, 111 sphinx (Asteroscopus), 123 sphinx (Brachionycha), 123 spini (Thecla), 11, 13, 15, 20, 56, 152, 271 spinula (Cilix), 228 splendana (Cydia), 318 spumosum (Stibadium), 193 stabilis (Teniocampa), 76, 125, 227 statices (Procris), 300 statilinus (Argynnis), 156 stellatarum (Macroglossa), 62, 90, 152 sticticalis (Phlyctenodes), 318 stigmosa (Scotogramma), 318 straminea (Leucania), 300 straminea (Pydna), 268 stratarius (Biston), 92 striata (Lycena), 251 striata (Polyommatus), 327 strigosa (Acronycta), 218, 251, 298, 299, 300, 314 strigosa (Hyboma), 218 strigillaria (Aspilates), 110, 111 strigula (Agrotis), 119, 120, 122, 254 strigula (Lycophotea), 119, 120, 122 stubbendorfii (Parnassius), 229 stygne (Erebia), 10, 11, 13, 14, 47, 57 59, 128, 282, 283, 284, 285, 312, 313 Styriaca (Parnassius), 111 suava (Hublemma) 63 subalpina (Chrysophanus), 10, 13, 57, 127, 207, 313 subapennina (Polyommatus), 17 *subfalcata (Gonanticlea), 292 sublustris (Xylophasia), 254, 300 submutata (Acidalia), 62 subobsoleta (Polyommatus), 327 *subornata (Mecodina), 223 subsequa (Tripheena), 110 subsericeata (Acidalia), 47 substrigilis (Oxyambulyx), 279 subtilata (Acidalia), 318 subtusa (Tethea), 110 suffumata (Cidaria), 157 suffumata (Lampropteryx), 111, 128 *suffusa (Kerala), 220 *suffusa (Perenia), 202 +] XXll sulphuralis (Phlyctsznodes), 318 superba (Westermannia), 169 suwarovius (Melanargia), 240, 296 sybilla (Limenitis), 17 sylvanus (Augiades), 13, 313, 317 sylvanus (Pamphilus), 20 Syngrapha, 183 syngrapha (Agriades), 17, 46 Synthymia, 183 Syrichtus (Hesperia), 126 syringaria (Hygrochroa), 120 syringaria (Pericallia), 120 tabidaria (Rhodostrophia), 62 tages (Nisoniades), 47, 206, 317 *taiwana (Anticlea), 203 *taiwana (Dindica), 292 *taiwana (Noctua), 152 *takaoensis (Parallelia), 319 Tambana, 183 tanaceti (Dichrorampha), 106 tanaceti (Hemimene), 106 taras (Syrichtus), 328 taraxaci (Caradrina), 254 tarpeia (Cineis), 242 tartaricus (Microbiston), 92 telicanus (Tarucus), 149, 156, 177 templi (Dasypolia), 38 tenebrosa (Rusina), 228, 253 Tephroclystia, 61 tessellum (Hesperia), 8, 241, 316 testacea (Luperina), 302, 303 tetralunaria (Selenia), 47 tetrica (Satyrus), 297 thalassina (Mamestra), 227, 254 tharos (Phyciodes), 195 thaumas (Hesperia), 10 thersamon (Chrysophanus), 272 thersites (Agriades), 13, 45, 46, 59, 157 thersites (Polyommatus), 273, 286, 309, 311, 313 thersites (Coenonympha), 19 thetis (Agriades), 13, 17, 20, 46, 47, 303, 327 thulei (Noctua), 275 tigelius (Pararge), 149, 151, 175, 177 tiphon (Ceenonympha), 46, 128, 226 tipuliformis (Sesia), 260 titania (Acontia), 317 tithonus (Epinephele), 14, 70, 149, 175, best trabealis (Emmelia), 317 tragopogonis (Amphipyra), 254, 302, 303 transalpina (Anthrocera), 311 transalpina (Zygena), 63, 205, 286 trapezina (Calymnia), 43 trapezina (Cosmia), 43 triangulum (Noctua), 260, 262 trifolii (Anthrocera), 47, 326 trifolii (Zygena), 160 trigeminata (Acidalia), 62 trigotephras (Orgyia), 62 trigrammica (Grammesia), 253 trilinea (Grammesia), 228 INDEX. trilinearia (Ephyra), 62 tripartita (Abrostola), 111, 253, 302 triquetra (Euclidia), 318 tristata (Melanippe), 108 Trisuloides, 183 trivia (Melitwa), 241, 295 truncata (Cidaria), 47, 48, 253, 303 tyndarus (Hrebia), 129, 284, 312, 313 typhon (Ccenonympha), 47, 110 ultimaria (Tephroclystia), 62 ulula (Dyspessa), 63 ulve (Senta), 300 umbratica (Cucullia), 228, 254 undata (Cauninda), 183 unicolorata (Ematurga), 251 unicolorata (Fidonia), 251 unilobata (Xanthorhoé), 323 unipunctalis (Pyralis), 152 uralensis (Anthocharis), 270 urticee (Abrostola), 111 urtice (Aglais), 10, 313 urticee (Vanessa), 38, 41, 133, 160, 276, 324 vaccinii (Orrhodia), 227 vafra (Scoparia), 135 valesiaca (Hrebia), 284 valezina (Dryas), 175, 176, 177 varia (Melitwa), 46, 58, 128, 313 variata (Thera), 72, 111, 120, 231, 253, 303 variegana (Peronea), 135 *variegata (Chytonix), 164 *variegata (Hadena), 162 variegata (Tambana), 183 varleyata (Abraxas), 47, 109, 111 vellida (Hepialus), 276 *venipicta (Acasis), 292 venosa (Chalcosia), 158 venosata (Eupithecia), 253, 275, 276 vernaria (Geometra), 62, 254 vernetensis (Zygena), 63 versicolor (Endromis), 38 yverticalis (Botys), 259 verticalis (Phlyctanodes), 318 vespiformis (Sesia), 260 vibicaria (Rhodostrophia), 62, 318 vibicigella (Coleophora), 318 villica (Arctia), 113, 114 viminalis (Bombycia), 254 vinula (Dicranura), 228 viretata (Lobophora), 47, 110 *virgata (Pydna), 266 virgauree (Chrysophanus), 10, 13, 57, 89, 127, 312, 313 virgularia (Acidalia), 46, 62 viridana (Tortrix), 241, 259 viridaria (Prothymnia), 62 viridata (Nemoria), 62 vitalbata (Phibalapteryx), 254, 302 vittata (Phibalapteryx), 72 vittata (Polyommatus), 18, 20 vittelina (Leucania), 110 volgaria (Kuchloris), 318 13, 128, 284, INDEX. *volgensis (Euchloé), 270 wahlbergi (Hypolimnas), 157, 158 w-album (Thecla), 271 *wardi (Arctia), 114 weidemeyeri (Basilarchia), 193 werdandi (Colias), 83, 270 xanthographa (Noctua), 38, 122, 302, 303 hogan (Segetia), 122 xantholopha (Macrobarasa), 220 xeranthemi (Cucullia), 318 Xxiil xylostella (Cerostoma), 259 Zale, 183 zapatosa (Sagana), 111 zephyrus (Plebeius), 44, 236 zermattensis (Chrysophanus), 312 zetica (Chalcosia), 158 ziczac (Notodonta), 71 zonaria (Ithysia), 92, 94 zonaria (Nyssia), 47, 110, 183, 207, 327 Zygena, 154, 229 Order XIX. COLEOPTERA. zeneus (Corymbites), 112 albicincta (Epitoxa), 43 argentatus (Phyllobius), 112 arietus (Clytus), 112 atra (Hispa), 158 betule (Deporans), 112 Bruchophagus, 53 brunnea (Crioceris), 279 cacaliz (Orina), 249 calcaratus (Phyllobius), 112 campestris (Cicindela), 46 centaurus (Archon), 158 communis (Amara), 112 constrictus (Desmoris), 196 conyergens (Hippodamia), 193 coriarius (Prionus), 104, 252 coryli (Strophosomus), 112 Crioceris, 228 domesticum (Anobium), 110 exclamationis (Chrysomela), 193, 196 fulvus (Desmoris), 196 gloriosa (Orina), 249 hemorrhoidalis (Athous), 112 hemorrhoidalis (Megarhinus), 280 *immsi (Psephenides), 189 interrupta (Episcaphula), 107 italica (Luciola), 228, 279 lilii (Crioceris), 279 Longicornia, 182 lunatus (Diphyllus), 77 marginatus (Dolopius), 112 melanocephalus (Calathus), 112 merdigera (Crioceris), 279 nubilus (Liophleus), 217 Order XXI. zstuum (Limnophora), 182 Anthocoris, 217 Banksinella, 112 bimaculata (Dictenidia), 218 calcitrans (Stomoxys), 131 caloptera (Laglasia), 107 chameleon (Stratiomyia), 112 ciliata (Fannia), 182 coccidivora (Diadiplosis), 86 crabroniformis (Asilus), 182 cyaniventris (Dermatobia), 131 Dermatobia, 131 oblongus (Phyllobius), 112 Orina, 249 pariseta (Thoricius), 107 Phytodecta, 249 picipes (Otiorrhynchus), 112 *picus (Hurytoma), 53 pilula (Byrrhus), 112 populi (Melasoma), 279 Prionus, 110 Psammechus, 110 *Psephenoides, 189 Psephenus, 188 Rhipiphorus, 188 rubi (Batophila), 217 rufipes (Phytodecta), 250 saxea (Stretchia), 163 schonherri (Barynotus), 112 sikore (Semiclaviger), 182 speciosa (Orina), 249 spinosus (Dectes), 195 staphylia (Chrysomela), 112 superba (Orina), 249 suturalis (Lochmea), 182 ulicis (Apion), 112 variabilis (Phytodecta), 249 viminalis (Gonioctena), 249 viminalis (Phytodecta), 249 violaceum (Apion), 112 virescens (Aidemera), 157 vittigera (Orina), 249 vorax (Apion), 217 whitei (Hudectus), 157 wisel (Goliathus), 157 DIPTERA. Dioctria, 216 domestica (Musca), 69, 131 fasciata (Stegiomyia), 37 fatigans (Culex), 37 fera (Tachinus), 182 finalis (Tephritis), 195 Glossina, 182 griseola (Macronychia), 182 grossa (Tachinus), 182 guttatus (Syrphus), 45 Hilara, 216 longipennis (Strauzia), 195 XX1V Mansonia, 37 minuta (Tachydromia), 216 morsitans (Glossina), 182 nobilitatus (Peecilobothrus), 218 obliqua (Allograpta), 131 pallidiventris (Tachydromia), 217 parvicornis (Chirosia), 182 Phormia, 192 potamida (Stratiomyia), 122 pseudoscutellaris (Stegiomyia), 37 Order XXII. abdominalis (Macrocentrus), 258 aceris (Phyllotoma), 46 Acroricnus, 23, 137 acuminata (Ccelioxys), 130 zquatus (Branchus), 138 sereus (Panargyrops), 120 affinis (Salius), 129 Agenia, 173 albatorius (Cryptus), 25 albiditarsis (Meteorus), 75 *altitudinis (Euryglossa), 213, 214 ambulator (Acroricnus), 170, 178 ambulator (Cryptus), 172 analis (Andrena), 130 angophore (Hxoneura), 200 annulicorne (Joppidium), 138, 141 annulipes (Mesoleptus), 25 annulipes (Syzeuctus), 25 antipodes (Binghamiella), 199 apicale (Joppidium), 138, 139 apicata (Andrena), 130 apparitorius (Cryptus), 25 approximator (Rhyssa), 22 ardens (Joppidium), 138 ardescens (Ccelioxys), 115 areator (Hemiteles), 77 arenaria (Cerceris), 252 argentata (Andrena), 130 asperithorax (Halictus), 307 atrator (Meteorus), 77 *atronitens (Parasphecodes), 242 aurantipennis (Megachile), 119 aurulenta (Osmia), 130 azteca (Ccelioxys), 116 barbifrons (Ichneumon), 37 Baryceros, 137 basalis (Ccelioxys), 119 basalis (Odynerus), 138 bellicosum (Joppidium), 138, 140 bellicosus (Cryptus), 140 bellosus (Cryptus), 140 beroni (Ccelioxys), 117 bibulus (Cryptus), 25 bicarinata (Colioxys), 116, 117 bicingulatus (Halictus), 307 bicolor (Exoneura), 200 bicolor (Mimesa), 129 bicolor (Osmia), 130 bifida (Nomada), 130 bimaculata (Anérena), 130 INDEX. pygmma (Lispe), 182 pyrophila (Sarcophaga), 280 saliciperda (Cecidomyia), 158, 182 *samoaensis (Pseudoteniorhynchus), 36 Sciara, 216 Sepsis, 192 Styringomyia, 182 Teniorhynchus, 37, 112 terre-nove (Phormia), 131 vibrans (Seoptera), 218 HYMENOPTERA. bimaculatus (Meteorus), 122 Binghamiella, 308 birenimaculatus (Odynerus), 173 borealis (Nomada), 130 botanica (Exoneura), 200 *bribiensis (Allodapa), 200 bruneri (Anthophorula), 114 Buathra, 25 ceruleipenne (Joppidium), 138, 139, 140 cesar (Lucilius), 130 calcaratus (Panurgus), 130 calliopsella (Euryglossa), 213 calliopsiformis (Huryglossa), 213 Callomelitta, 308 campestris (Ammophila), 224 campestris (Gorytes), 129 capensis (Osprhynchotus), 24 capitatus (Ccelioxys), 119 capitosus (Crabro), 129 cetii (Andrena), 130 chapmani (Halictus), 243 chichimica (Ccelioxys), 118 chloropthalma (Bracon), 289 chloropthalma (Zele), 287, 288, 289 chloropthalmus (Phylax), 289 chloropthalmus (Rhogas), 288, 289 chrysopthalmus (Meteorus), 76 chrysosceles (Andrena), 130 circumcincta (Megachile), 130 circumdatus (Halictus), 243, 307 Closterocerus, 123 cloutieri (Acroricnus), 171 coarctata (Humenes), 130 Ceelioxys, 118 ceruleipenne (Joppidium), 138, 139, 140 cognatus (Halictus), 307 collaris (Bracon), 261 collaris (Macrocentrus), 258, 261, 262, 287 compactula (Anthophorula), 114 confusa (Prosopis), 130 contracta (Ponera), 131 coquilletti (Anthophorula), 114 corniger (Passalecus), 129 *costaricensis (Ccelioxys), 117, 118 *crabronica (Kuryglossa), 142, 199 crassimanus (Mesochorus), 120 Cryptus, 25, 137 cupulifera (Allodape), 119 deceptor (Meteorus), 76 INDEX. decoloratus (Meteorus), 123 depilis (Iridomyrmex), 192 destillatorium (Sceliphron), 172 Diadasia, 115 *disclusus (Halictus), 243 discolor (Zele), 287, 290 Distantella, 23 donabile (Joppidium), 140 donabilis (Joppidium), 140 dorsata (Andrena), 130 Dorylus, 107 dubiosum (Joppoceras), 137, 138 edwardsi (Acroricnus), 171 elegans (Acroricnus), 170 Entedon, 123 *Epiteropia, 68 equalis (Macrocentrus), 258, 261 equestris (Mimesa), 129 Euceros, 137 Eulophus, 123, 216 Eumenes, 171 europxa (Mutilla), 129 Euryglossa, 308 Kuryglossidia, 198 Examolopis, 115 Exoneura, 308 extensor (Hubadizon), 260 5-fasciata (Cerceris), 129 femorata (Lissonata), 217 filator (Meteorus), 74, 124 filicornis (Hedycryptus), 25 flavipes (Osprhynchotus), 24, 27, 28 flavus (Lasius), 107 fragilis (Meteorus), 124 *frederici (Exomalopsis), 115 fugax (Solenopsis), 43 fumidicauda (Parasphecodes), 243 furcatus (Podalirius), 130 fusca (Formica), 45 fuscipenne (Joppidium), 138, 139, 140 fuscipennis (Cryptus), 140 fuscipes (Andrena), 130 gallica (Polistes), 228 *gseminator (Zele), 287, 289 geniculatus (Certonotus), 230 gigas (Osprhynchotus), 24, 26, 27, 28 gilesi (Halictus), 307 Halictus, 308 *hematopus (Halictus), 307 hemorrhoidalis (Cilissa), 130 hamulata (Exoneura), 200, 308 hattorfiana (Andrena), 130 hedleyi (Halictus), 244 Hedyeryptus, 25 *hemichlora (Euryglossa), 214 herrichii (Odynerus), 130 himalayensis (Cryptus), 25 hirtipes (Dasypoda), 251, 252 Homolobus, 257, 287 Hyleoides, 142 Ichneumon, 137 ichneumonides (Kuryglossidia), 198 ichneumonides (Methoca), 129 XXV ictericus (Meteorus), 76 inconspicua (Euryglossa), 215 indicus (Cryptus), 25 infirmus (Macrocentrus), 258, 261 *infumator (Zele), 287, 288, 290 insidiator (Cryptus), 25 instabilis (Halictus), 243 *insularis (Binghamiella), 199 *insularis (Exoneura), 200 interruptus (Crabro), 130 interruptus (Nysson), 129 itinerans (Iridomyrmex), 192 jonellus (Bombus), 129 Joppa, 137 Joppidium, 137, 170 Joppoceras, 137 junceus (Acroricnus), 170, 174 junceus (Cryptus), 173 klugianus (Podagrion), 263 labiata (Macropis), 130 Labrorychus, 230 lacticinctus (Gorytes), 129 . levipes (Odynerus), 130 lanarius (Halictus), 307 *latissima (Kuryglossa), 215 *launcestonensis (Paracolletes), 305 leaiana (Osmia), 218 leporina (Cilissa), 130 leporina (Ceelioxys), 117 leucochrysea (Ccelioxys), 117 leucomelana (Osmia), 130 leviventris (Meteorus), 125 ligniseca (Megachile), 130 linearis (Rogas), 259 Linoceras, 23, 170, 172 Lissonota, 218 *littleri (Callomelitta), 305 *littleri (Halictus), 307 lituratus (Crabro), 130 luctuosa (Melecta), 130 luculentus (Cryptus), 25 luridus (Meteorus), 124, 125 *luzonicus (Ccelioxys), 118 macrobatus (Acroricnus), 170, 171 macrobatus (Cryptus), 171, 173 Macrocentrus, 257 macrocercus (Ichneumon), 140 maculata (Kuryglossa),214 maculatus (Cer_pales), 129 merens (Nomia), 307 marginata (Allodape), 119 marginator (Macrocentrus), 258, 259, 261 marginatus (Paracolletes), 305 Megachile, 308 melanoleucus (Acroricnus), 170, 173 melanoleucus (Cryptus), 172 melanoleucus (Linocerus), 172 *melanopterus (Halictus), 243 *melanosoma (Huryglossa), 214 melanostictus (Meteorus), 74, 120 mellifer (Apis), 192 Meteorus, 74, 122 *morgani (Anthophorula), 114 XXV1 INDEX. nebriceps (Joppidium), 138 niger (Meteorus), 120 nigra (Euryglossa), 215 nitidifrons (Kuryglossa), 199 nitidipennis (Cryptus), 140 Nomia, 308 nursei (Cryptus), 25 objurgator (Cryptus), 25 objurgator (Ichneumon), 25 objurgator (Osprhynchotus), 24, 25 obliteratus (Ichneumon), 37 obscurus (Cryptus), 26 *occidentalis (Exoneura), 200 Odynerus, 130, 173 Ophion, 287 orientalis (Cryptus), 25 Osmia, 171 Osprhynchotus, 23, 170 otomita (Ccelioxys), 115, 116 Oxybelus, 129 pachymerum (Podagrion), 263, 265 pachymerum (Priomerus), 263 Pachitomus, 263 pallipes (Macrocentrus), 259 Paniscus, 287 Paracolletes, 308 Parasphecodes, 308 Passalecus, 218 Pemphredon, 218 perhumilis (Prosopis), 306 Perilampus, 120 peronatus (Acroricnus), 170, 172 peronatus (Osprhynchotus), 23 persuasoria (Rhyssa), 21, 22, 225 philippensis (Ccelioxys), 119 Phygadeuon, 137 picta (Callomelitta), 305 pictus (Odynerus), 130 pilapes (Andrena), 130 pilicornis (Osmia), 130 pilosella (Distantella), 25 planiceps (Exomalopsis), 115 plorator (Parasphecodes), 243 Podagrion, 263, 264, 265 porrectorius (Habrocryptus), 172 preecox (Andrena), 130 prasinus (Halictus), 130 prolongata (Xyphydria), 22 Prosopis, 308 Protelus, 74 pulcher (Acroricnus), 170 pulcherrimus (Cryptus), 27 pulcherrimus (Osprhynchotus), 24, 27 pulchricornis (Meteorus), 74, 76,119, 121 *purpurascens (Euryglossidia), 197, 198 Pyramishyssa, 230 quadridentata (Ccelioxys), 150 quadrifasciatus (Gorytes), 129 quercina (Ccelioxys), 116 rectangulata (Huryglossidia), 198 religiosus (Palmon), 263 *reticulatithorax (Epiterobia), 68 reticulosus (Sphecodes), 130 retusus (Podalirius), 130 *rhodopterus (Parasphecodes), 306 Rhyssa, 20, 32 ridens (Euryglossa), 214 roberjeotiana (Nomada), 130 rose (Andrena), 130 rubiginosa (Euryglossa), 214, 215 rubriceps (Joppidium), 138, 139 ruficeps (Osprhynchotus), 24, 27 ruficolle (Joppidium), 139 ruficornis (Xenodocon), 171 ruficrus (Apanteles), 225 rufipes (Epeolus), 130 rufiventris (Buathra), 25 *rufotegularis (Parasphecodes), 306 sabulosa (Ammophila), 225, 251 sanguinea (Formica), 129 sanguinipes (Halictus), 307 sanguinosus (Ccelioxys), 116 Sceliphron, 172 schenki (Cremastogaster), 181, 182 scutellator (Meteorus), 121, 122 seductor (Acroricnus), 170, 171 seductor (Ichneumon), 171 *semisanguineus (Scelio), 197 sexfasciata (Nomada), 252 signatus (Crabro), 129 simiatus (Odynerus), 130 similis (Andrena), 130 smaragdina (Cicophylla), 157 solidaginis (Nomada), 252 solskyi (Stigmus), 129 *sonorensis (Coelioxys), 116 spinigera (Andrena), 130 spinulosa (Osmia), 30 spirifex (Pelopseus), 171 stuchila (Paraphecodes), 306 subterranea (Aphenogaster), 107 subulosus (Mellinus), 129 *submerans (Nomia), 307 succinetus (Colletes}, 130 . sulcinodis (Myrmica), 129 sumatrana (Ccelioxys), 119 syriacus (Acroricnus), 23, 170, 172 syriacus (Osprhynchotus), 172 taluchis (Parasphecodes), 306 tarsoleucus (Cryptus), 25 tasmaniz (Halictus), 244 Terobia, 68 testaceator (Zele), 76, 287, 288, 289 tetricus (Mesochorus), 120 texana (Anthophorula), 114 texana (Ccelioxys), 116 Thalessa, 22 thoracicus (Macrocentrus), 258, 259, 261 tibialis (Crabro), 129 totonaca (Ccelioxys), 118 Trichiosoma, 157 Trigona, 192 trinotata (Distantella), 24 *triodonta (Ccelioxys), 117 tropica (Ceratina), 119 tumorifera (Ccelioxys), 117 *turneri (Exoneura), 199 *undulata (Kuryglossa), 198 unicolor (Allodape), 201 unicolor (Meteorus), 122 unicolor (Pompilus), 129 uniglumis (Oxybelus), 129 ursinus (Panurgus), 130 vagus (Crabro), 130 variegatus (Sphecodes), 130 INDEX. viaticus (Myrmecocystus), 107 villosula (Euryglossa), 199 violator (Ichneumon), 24 violator (Osprhynchotus), 24 virescens (Cicophylla), 157 Xenodocon, 170 yucatanense (Joppidium), 140 versicolor (Megachile), 130 Zele, 76, 257, 287 versicolor (Meteorus), 74, 122, 123 Zemiotus, 74 vexator (Meteorus), 77 P P wall easel: 1312. 1, Psigey Seite ADDENDA. 33, after megera add Satyrus cordula. HWRRATA, 25, for pherestes read pheretes. 5, for cordulea read cordula. 38, for eighty-nine read ninety. 20 from bottom, for climene read clymene. XXVli af i fy ie ; y aa Te my is wrt e ‘Entomologist’ (6s. post free) for 1914 are now due tO” oe Negman a C0. 54, i gic! Garden, si: fat ee 1914, (No. 608. EA Aes bh eae i # ENTOMOLOGIST q a a . “Wlostrain : Mont Journal ene | . OF en OR EET & aor a ra | a] i) b | GENERAL ENTOMOLOGY. Al EDITED’ BY RICHARD SOUTH, .F-E.S. . i ; , : ‘ WITH THE ASSISTANCE OF ie ' ) ha) Ries ah h ROBERT ADKIN, ¥.E.S. | C.J, GAHAN, M.A., F.E.S. fi HB. ROWLAND-BROWN, M.A.,F.E.S.| W. J. LUCAS, B.A., FES, a OW. L. DISTANT, F-E-S., &c. CLAUDE MORLEY, ®.E.S., F.Z.S. || FF. W. FROHAWK, F.E.S., M.B.0.U.| Dr. D/ SHARP, F.R.S., F.B.S., ko. { Pgs " vu ‘‘By mutual confidence and mutual aid Great deeds are done and great discoveries made.) ot ; 3 LONDON: | rte WEST, NEWMAN & CO., a4, HATTON Naa kivien | SIMPKIN, MARSHALL, HAMILTON, KENT. & CO., Limrrep. \ | ©... DOUBLE NUMBER—Price One Shilling. WATKINS & DONCASTER Naturalists and Manufacturer of Entomological Apparatus and Cabirets. i Plain Ring Nets, wire or cane, including Stick, 1s. 3d., 28., 28.6d. Folding Nets, 38. 6d., 48; Umbrella Nets (self-acting), 7s. Pocket Boxes, 6d,, 9d., 1s., 1s 64. Zine Relaxing Boxes, 9d., 1s., 1s. 6d., 28.. Nested Ohip Boxes, 7d. per four dozen, Entomological Pins, assorted or mixed, ls., 1s. 6d. per oz. Pocket Lanterns, 2s. ile to 8s. Sugaring Tin, with brush, 1s. 6d., 2s. Sugaring Mixture, ready for use, ls. 9d. per tin. Store Boxes, with camphor cells, 2s. 6d., 48., 5s., 68. Setting Boards, flat or oval, 1 in., 6d.; 1} in., 8d.; 2 in., 10d.; 2}in.,1s,; 84in., Is. 4d.; 4 in., 1s. 6d.; 6 in., 1s. 10d.; Complete Set of fourteen Boards, 108, 6d. Setting _ Honses, 9s. 6d., 11s. 6d.; corked back, 14s. Zine Larva Boxes, 9d., Is., 18. 6d. Breeding Cage, 2s. 6d., 4s8., 58., 78. 6d. Ooleopterist’s Collecting Bottle, with tube, 1s. 6d., 1s. 8d, Botanical Oases, japanned, double tin, 1s. 6d., 28.9d., 8s. 6d., 4s, 6d, Botanical Paper, 1s. 1d., 1s. 4d., 1s. 9d., 28. 2d., per quire. Insect Glazed Oases, 2s. Gd. to 11s. Oement for replacing Antenne, 44. per bottle. Steel Forceps, 1s. 6d., 28., 28.6d. per pair. Cabinet Cork, 7 by 84, best quality, 1s. 6d. per dozen ~ sheets. - Brass Chloroform Bottle, 2s. 6d. Insect Lens, 1s. to 8g. Glass-top and Glass-bottomed Boxes from 1s. per dozen. Zine Killing Box, 9d., 1s. Pupa Digger, in leather sheath, 1s. 94. Taxidermist’s Companion, containing most — necessary implements for skinning, 10s. 6d. Bealpels, 1s. 8d.; Scissors, 28. per ‘pair; Wgg-drills, 2d., 34., 94.; Blowpipes, 4d., 6d.; Artificial Eyes for Birds and Animals; Label-lists of British Butterflies, 2d.; ditto of Birds’ Eggs, 2d., 3d., 6d.; ditto of Land and Fresh-water Shells, 2d.: Useful Books on Insects, Eggs, &e. . SILVER PINS for collectors of Micro-Lepidoptera, &¢., as well as minute insects of all other families. ' We stock various sizes and lengths of these Silver Pins, which have certain — advantages over the ordinary pins, whether enamelled, black, or silvered or gilt. For instance, insects liable to become greasy, and verdigrisy like Sesiidx, &c.,. are best pinned on Silvar Pins, which will last much longer. We shall be pleased to send patterns on application. SHOW. ROOM ‘FOR CABINETS Of every description for Insucrs, Bixps’ Eaas, Coins, Microscopical OpyEcrs Fossiis, &e. Oatalogue (100 pp.) sent on application, post free. A LARGE STOCK OF INSEOTS AND BIRDS’ EG@sg — (BRITISH, KUROPEAN, AND EXOTIC), Birds, Mammals, éc., Preserved and Mounted oy Firet-claaz Workmen. 36, STRAND, W.C., LONDON, ENGLAND. MY NEW REVISED PRICE ‘LIST. OF SET ; " BRITISH LEPIDOPTERA now being issued, Write at once if you have not received one. : Fine bred Yellow Dominula, 5s. each. Corydon var. Semisyngrapha, ds. each. Trish specimens (this year’s) Artemis, 2s. 6d. per doz. Minos, 7s. per doz. Hippocrepidis, 5s, per doz. Napi, 3s. 6d. per doz. ; and many others, ~ My Text Book, the ideal work for Collectors: life-history and food-plants of every species, 3s. 9d. post free. Newman's Electric Lamp, specially designed for collectors, gives 18 hours’ _ continuous light, 8s. 6d., postage 4d.; new batteries Is, each, postage 3d, — 3 L. W. NEWMAN, F.E.S.. BEXLEY, KENT, ‘ F R SALE. — Lane’s ‘ Butterflies of Europe,’ | 2 vols. as new (published at £3 18s.), 50s, Tutt’s ~ ‘ British Lepidoptera,’ 8 vols. (published at £8) ,75s. Morris’s ‘ British — Moths,’ 4 vols., 35s. Ten-drawer Cabinet (Crockett), (cost £6), 75s. ~ Twelve-drawer do. (cost £9), £5 10s. Sixteen-drawer do, £6." Also @ sixteen-drawer Cabinet, £6 10s. ; = A. FORD, 86, IRVING ROAD, BOURNEMOUTH. THE ENTOMOLOGIST Vou. XLVIL1 JANUARY, 1914. [No. 608 SOME REMARKS ON THE ATLANTIC FORMS OF SYMPETRUM STRIOLATUM, Cuarp. By Kenneto J. Morton, F.E.S. In the ‘ Revue des Odonates’ (1850), p. 43, in discussing the Libellula ruficollis of Charpentier, de Selys writes as follows :— ‘*M. Hagen m’a communiqué deux des trois exemplaires types recus de Portugal par M. de Charpentier ; ce sont de vrais strio- lata males trés adultes, mais en mauvais état de conservation. i Les pieds sont comme tournés au gras et les lignes jaunes sont trés-étroites, surtout sur les cuisses (qui au premier abord paraissent noirdtres), mais elles existent. la taille est trés grande, mais pas sans exemple en Belgique.”’ Lower down on the same page we read: “‘J’ai vu dans la collection de Miss Ball a Dublin, des exemplaires males adultes qui avaient aussi les pieds trés-peu lignés de jaune.” In the “‘ Revision des Diplax paléarctiques ”’ (‘ Annales de la Soc. Ent. Belg.,’ xxviii. p. 85 (1884), de Selys describes a race of S. striolatum from Madeira under the name of nigrifemur, of which he says:—‘‘ Les femurs sont noiratres sans ligne jaunatre, et aux tibias le jaunatre n’occupe qu’une raie externe étroite. La taille est trés grande: abdomen ff 27: 2 26-29. Aijle inferieure ¢ 30-33; ¢? 30-83... les parties noiratres des cotés du thorax sont trés foncées, de sorte que. les deux bandes jaunatres qui les divisent, sont fort tranchées.” These are the first indications of the existence of what may be termed an Atlantic race of S. striolatum characterized by darker femora, and usually by more strongly pronounced lateral thoracic markings than in the more typical forms. The next occasion on which exceptionally dark S. striolatuwm are alluded to, the insects in question came from a somewhat unexpected and in some respects rather remote point, and the imagination of those who had to do with them seems to have been rather exercised concerning them. Mr. Lucas in ‘ Entomologist,’ May, 1900, p. 1389, recorded the capture at Stornoway by Mr. Fremlin of two females of a Sympetrum, and wrote of them as follows :—‘‘ The conclusion to which we must come, seeing there are two specimens thus pre- ENTOM.—JANUARY, 1914. B 2 THE ENTOMOLOGIST. cluding an aberration, appears to be that the insects belong to a form of S. striolatum somewhat resembling S. scoticum (probably a local race), or else that both insects are hybrids between the two species. Mr. McLachlan, who has examined the insects, ae to the latter opinion.” A good figure accompanies this record. Further, in ‘ Entomologist’ for June, 1912, p. 171, Mr. Lucas records a pair of dragonflies captured by Colonel Yerbury at Lochinver, Ross-shire (I presume Sutherland is meant), which are said to be the very counterparts of the Stornoway specimens. He gives to these examples the name of S. nigrescens, and con- siders them either a new species or a very distinct race of striolatum. In his remarks there seems still to be a tendency to associate the insects in some way with S. scoticum, and one is tempted to regard his description as a little forced to maintain this. Unfortunately Mr. Lucas does not compare his specimens with those from other localities in Scotland, England, Ireland, or elsewhere. There is accordingly room for some further observations. When Mr. Lucas’s original remarks appeared in 1900 I was not greatly interested in the subject. In 1912 his suggestion of the existence of a species of Sympetrum localized in the extreme north-west of Scotland seemed inconceivable, and considering the known powers of Sympetrum as a flier, the idea of a local race restricted to the same region was almost equally difficult to accept. After comparing the description with that of the var. nigrifemur, which it at once recalled, I gave the matter no further consideration until I received an enquiry from Dr. Ris asking me what I knew of S. nigrescens, the description of which had been brought under his notice by Mr. Herbert Campion. With the ready co-operation of my friend and neighbour Mr. William Evans, I was able without any delay to send Dr. Ris speci- mens from the west of Scotland evidently similar to Mr. Lucas’s, and, together with these, series of S. striolatum from the north of Ireland and the New Forest for comparison. Since then, by the kind assistance of friends and correspondents, I have examined quite a number of examples from different localities, and the conclusion come to is that the form described by Lucas extends with a certain amount of variation, both individual and local, over the whole western fringe of Scotland; while examples from Ireland, especially from the north and west, although more variable and in some respects intermediate, still retain some of the same characters, and in any breaking up of the species into races would fall to be associated with the Scottish form rather than with the typical one. Fortunately Dr. Ris visited Brussels in the autumn, and was able to re-examine the types of nigrifemur. His conclusions on the whole subject will appear in the additions to his great work on the Libelluline, but I believe that I have ATLANTIC FORMS OF SYMPETRUM STRIOLATUM, CHARP. 3 his sanction to state that our Scottish insect will fall in his revision of S. striolatum under the subspecies nigrifemur. Just after sending the material to Dr. Ris, Mr. G. G. Black- wood, of Edinburgh, brought to me most opportunely a very nice little series (four males, one female) of S. striolatum, in very mature condition, which he had taken at Mallaig, Inverness- shire, on September 4th last; and having found it useful to tabulate the principal characters of these and of the more typical English form, I give here a reproduction of this tabulation in part, along with two diagrams showing the lateral thoracic markings, taken respectively from males from Thorney, Cam- bridgeshire (Fig. 1) and Mallaig (Fig. 2). EneuisH. (Male.) WESTERN ScortisH. (Male.) Line at base of the frons ends at the Line extends downwards somewhat, eye, without going downwards. as in vulgatum. Humeral and second lateral sutures Humeral suture more heavily marked very narrowly marked with black. The first lateral suture in its upper part hardly marked at all (some- times, however, the narrow median field (F, G) may be lightly outlined in fuscous). Usually five fairly well-defined yel- lowish spots surrounded by black on the sides of the thorax above the legs. These spots are distri- buted thus on . | mesinfrepisternum. c: mesepimeron. D . . = metinfrepisternum. This field is the metepisternum, | and in the typical forms is not divided into spots. The above spots may be more or less confluent; thus a, B may be con- fluent or just separated by a narrow neck, rarely quite separate; Cc may touch E or may be distinctly sepa- rate; D may be partially confluent with E or narrowly separated. Sternum mostly yellowish, the sutures sometimes marked with blackish. with blackish. Narrow middle field usually strongly outlined in fuscous and divided by a broad diagonal line, the two enclosed spots (F, G) varying in size, but the one nearer the stigma always smaller and triangular. Note.— Even in an otherwise very dark example, the infuscated outline of the middle field is slight and the diagonal division hardly marked. Spots A, B, C, D,E variable, but all much reduced in size, and in the Mallaig examples never confluent. Sternum mostly blackish posteriorly, with a yellowish oval marking on either side of the middle line, these markings diverging caudad and having a yellowish tail (the black condition is no doubt in part the result of age), B 2 4 THE ENTOMOLOGIST. Eneutsu. (Male.) WESTERN ScortrisH. (Male.) Trochanters with a large black spot; Legs in the Mallaig specimens prac- femora and tibie externally yel- tically all black except distal half lowish, the yellow on femora of anterior trochauters and the yel- divided by a strong black line. low lines on all the tibize. While there is no reason to doubt that the legs are much blacker always than in the typical forms, there is here and there just the faintest trace of yellow on the femora, the relics of a certain amount of that colour which has become gradually obliterated through age (see on this point the slight discrepancy in Mr. Lucas’s two descriptions). Abdomen beneath marked longitudi- Very broad black markings occupy nally with black. the greater part of each side of the ventral suture, the red being re- duced to mere streaks. Rounded spots near genitalia small. Black lateral longitudinal mark- ings much more strongly developed than in the typical forms. Hind wings 27-30 mm. Hind wings 25°5-27 mm. Two males (coll. W. Evans), Glen Aros, Mull (August 6th), and Morvern, Argyllshire (July), agree very well with the Mallaig examples, that from Mull being especially dark. A female from Moidart, Inverness-shire, in September (coll. Evans), has the thoracic spots rather larger, and the femora distinctly lined with yellow. A fine male from Talladale, Loch Maree, Ross-shire (August 11th), which has the sides of thorax very darkly marked, has distinct narrow yellow lines on the femora, while a female also from the Loch Maree district is very similar to the Moidart female (male and female, coll. J. J. F. X. King). Two very small specimens (male and female, the latter teneral, hind wing, male, 24 mm.) are also in King’s collection, without label, but ATLANTIC FORMS OF SYMPETRUM STRIOLATUM, CHARP. 5 believed to be from the island of Coll. In these the boundaries of the middle field are heavily shaded, and the legs are narrowly lined with yellow. Further, Mr. King reports two males from the island of Islay (July 18th), which are of the true western Scottish form, the lateral markings of thorax agreeing with diagram No. 2, excepting that spot @ is rather larger, the dark boundary of the upper part of the field being narrow. Three examples from Tayvallich, in Kintyre, deserve special notice (two males and one female, coll. A. M. Stewart, Paisley). The tendency of the line at the base of the frons to go down- wards is not so much pronounced, being more strongly marked downwards in the female than in the males. ‘'he narrow middle field of the thorax is distinctly outlined in fuscous, but the diagonal line is less clearly developed (partly, I think, a matter of age). Thoracic spots rather larger than in the northern examples, but c, p, E always well separated by broad black margins; in one male a and B widely separated ; in the other two connected by a narrow neck. The yellow spots on the metasternum long oval, the yellow tails becoming definite long wedge-shaped markings; following these is an irregular semi- circular black marking of varying breadth, the space enclosed being yellowish, but tending to become fuscescent and probably becoming blackish with age. In the males the narrow yellow lines on the femora are distinct ; but in the female they tend to become infuscated. Ventral surface of abdomen perhaps some- what discoloured, but apparently not differing from the northern specimens, and in great part black. . The above are from the northern part of Kintyre, and they constitute a natural link with the Irish forms. The extreme southern point of the long peninsula of Kintyre is only a matter of twelve and a half miles distant from the Irish coast, surely a mere trifle to a migrating Sympetrum. From Emyvale, Co. Monaghan, Ireland, I have before me a series of four males and three females. They are rather young, but they have much in common with the Scottish forms. The femora are lined with yellow, but the legs are over all darker than in the typical forms. The thoracic lateral spots are variable in size, but in some they are quite as small as in some of the Scottish specimens; A, B, c, D, E are completely isolated in all of them; the narrow middle field is always outlined in fuscous, and in three of them (one male and two females) the diagonal line is clearly marked. Six of these have more or less dark shading at the side of the eye. By the very kind assistance of Mr. J. N. Halbert, I have been able to examine a series of specimens obligingly lent by the National Museum, Dublin, and originating from many different points in Ireland. They are from the following localities, viz. :— Males (one from each locality) :—1. Rostrevor, Co. Down, 6 THE ENTOMOLOGIST. September 2nd. 2. Dublin. 38. Cappagh, Co. Waterford. 3a. Cappagh, Co. Waterford (coll. J.J. F. X. King). 4. Cappo- quin, Co. Waterford, August 8rd. 5. Glencar, Co. Kerry. 6. Caragh Lake, Co. Kerry, July 30th. 7. Killarney, Co. Kerry, July 15th. 7a. Killarney, Co. Kerry, August 7th (coll. King). 8. Mallaranny, Co. Mayo, July. 9. Westport, Co. Mayo. 10. Clare Island, Co. Mayo, July. 11. Achill Sound, Co. Mayo. 12. Coolmore, Co. Donegal. 138. Derry. 14. Poyntz Pass, Armagh, September 26th. Females (one from each locality) :—1. Cappagh, Co. Water- ford. 2. Waterville, Co. Kerry, July 27th (teneral). 8. Park- naskilla, Co. Kerry. 4. Westport, Co. Mayo. 5. Ardara, Co. Donegal. Hind wing, male, 263-28 ; female, 274-29. In analysing the above, it may be said, with regard to the males, that the femora are in the darker condition alluded to under the Emyvale specimens, any exceptions being unimportant. The thoracic spots a, B, c, D, H (with one or two exceptions where A, B are nearly connected) are of variable and usually moderate size, but they are practically always completely isolated, and in 6, 9, and 11 run rather small, approaching the Scottish form. The middle field of the thorax, however, is frequently hardly outlined at all; this is the case in 1, 2, 3a, 4,5, 6; in the others it is outlined, although sometimes rather faintly; in 9 strongly, with traces of the diagonal line. The sternum, in nearly every case, is marked with black, sometimes rather strongly; and the under side of the abdomen seems much blacker as a rule, especi- ally in the anterior segments, than in the more typical forms. The shading at the side of the eyes is more or less marked in 3a, 6, 7, Ta, 9, 12, 13, 14, and in the others hardly or not at all indicated. The females are less satisfactory in condition. The thoracic spots A, B, 0, D, E are all isolated except a, B in 1, 2, 4, in which they are narrowly connected ; the middle field is always outlined. Further Irish material in Mr. King’s collection, examined by him, seems to be very constant in regard to the generally darker condition of the legs, and also the usually darker condition of the under side of the abdomen, but is in other respects variable. In a male from Wexford; male, Westport; male, Killarney, and two males from Cappoquin, the lateral markings of the thorax are much as in diagram No.1; while females from Killarney and Cong, Co. Mayo, are almost similar in that respect. One female from Athlone is almost a typical striolatum as regards the thorax; another from the same locality is an intermediate. One from West Meath has the middle field outlined in fuscous, while another from the same county is described as very near to an example from Islay. Three males from the Isle of Man, also sent by the Dublin LIFE-HISTORIES OF HESPERIA TESSELLUM AND H. CRIBRELLUM. 7 Museum, are interesting. They tend towards the intermediate condition, the spots, especially c, p, z, being smaller and the legs darker than in the typical form. Finally, a female taken by myself at Christiansand,.Norway (June 17th), may be mentioned. Although very young and the infuscation of the yellow on the femora only slight, the nigri- femur characters hold good in respect of spots a, B, c, D, B being all well separated, the fuscous outline of the middle field being heavily marked, the diagonal line being also broad and well defined. Hind-wing 27 mm. The distribution of Sympetrum striolatum in Scotland has been fully and carefully worked out by Mr. Evans (‘‘ Odonata of the Forth Area,” Proc. Roy. Physical Soc., xvi. pp. 87-96, 1905, and ‘Annals Scot. Nat. Hist.,’ 1911, pp. 14-25). It seems worthy of notice that, while the species apparently occurs all along the western seaboard of Scotland, including at least the larger islands, it is found rarely in the east of Scotland, and almost certainly does not breed there. Further, I am inclined to believe that the ordinary northern limit of S. striolatum as a British breeding species on the east coast must be drawn con- siderably south of the Scottish border, probably about the Humber, but further observations are required to verify this. Mr. Porritt says that he has no doubt that the species breeds regularly in the low-lying lands at Askern and probably all over that (the Doncaster) district, but not in the hilly districts of the county, 7. e. north, north-east, east, and most of the south-west, although it seems to occur sporadically in most parts of the county. He also thinks it may breed in the Hull and Goole district, although he has never seen it there. Ireland and the west of Scotland have in common a com- paratively mild and moist winter climate, and this condition may not only render possible the existence of S. striolatum in the west and north, while it fails on the east coast of our country, but also account for its melanic tendencies. Very likely these tendencies vary from season to season, and no doubt the infiux of migrants from other areas has something to do with the presence of intermediates. 18, Blackford Road, Edinburgh: November, 1913. NOTES ON THE LIFE-HISTORIES OF HESPERIA TESSELLUM AND dH. CRIBRELLUM. By tHe Hon. N. Caarues Roruscuinp, M.A., F.E.S. Herrn Hermann Ranenow, when recently collecting in the Ural Mountains, was fortunate enough to discover the larve and food-plants of the above-named insects, and has permitted me to record his observations in this Journal. 8 THE ENTOMOLOGIST. Hesperia tessellum. Caterpillars were found from the middle of May to the 10th of June on a species of Phlomis (certainly from the description, P. tuberosa). The larve spin the two edges of a leaf together on the upper surface, and live within this leaf. The colour of the larva is mouse-grey, with a black head and yellow collar. There are two black rows of dots on the back, an excellent characteristic of the species. The imago begins to emerge after the middle of June, and there is apparently a partial second brood in the beginning of August. Hesperia cribrellum. The larva of this species is indistinguishable from that of H. carthami var. meschlert, and lives spun up among the leaves of a species of Potentilla. The caterpillar is full-fed in May, and the imago emerges at the beginning of June. A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. By H. Rowuanp-Brown, M.A., F.E.S. (Continued from vol. xlv. p. 17.) (iv) Isére and Dréme. The Vercors. AFTER a year’s silence on the subject of ‘‘ fresh woods and pastures new”’ explored in France, I am again able to take up my pen to continue the series of short papers published by me in the ‘Entomologist’ for 1911-12. And I am the more encouraged to do so when I hear that my brother naturalists and collectors not only read these papers, but actually follow in my footsteps; - and this at other seasons of the year than those of my travel. So that, as time goes on, we may hope to obtain not only a fleeting record of the captures and observations of a week or two spent in the several localities, but a solid contribution to the knowledge of the lepidoptera occurring there from year’s end to year’s end. Most of us are compelled to do our collecting at fixed times of the year—usually in July and August—in the holiday season in fact. It has seldom fallen to my lot to get abroad before the last week of June, when the first flight of most of the southern species of the plains is over. And this year I did not leave London before July 1st. For some time past I had had my entomological eye, so to speak, fixed on the western Dauphiny, that is to say, the country west and south of Grenoble, between the Isére and the Drome, and within the departments bearing the names of the respective rivers. An application to the Cyclists’ Touring Club of France for information of this region brought me among other fascinating A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 9 booklets that published by the ‘‘ Syndicat d’Initiative de Valence- sur-Rhone et dela Drome.” A glance at its contents decided me to try the country known collectively as the Vercors, and a cyclist friend having passed through the Lans valley earlier in the summer and given satisfactory account, I took the morning tourist-car from Grenoble on July 2nd, one of the many now ‘*‘doing”’ the Alps and outlying ‘‘ massifs’’ in connection with the P.L.M. and Sud Railways. By these means rapid communi- cations have been opened up with well-known entomological centres, and a vast region of new country placed within easy reach of the main lines. But after five weeks’ experience of them I cannot say that I view the automobile alpine—by the way the Academy is divided as to whether it is masculine or feminine—as an unmixed blessing. From the tourist’s point of view the cars travel far too swiftly—it is impossible to enjoy the scenery ; while at present many of the mountain roads are wholly unfit for motor traffic, and the shaking amounts to positive torture of mind as well as of body. For when the setting boards are full the anxious collector is speculating all the time how many pins have got loose in the boxes, and trembling for the fate of his rarities. On several occasions, notably on the road from Barcelunnette to Prunieéres, the railway station on the Briancon line, irreparable damage was done in the way of broken antenne and split wings. Those who do their setting, as I do, en route will do well, therefore, to examine the boards before and after any involuntary game of Cup-and-Ball ofthe kind. Further, the turns and twists of the mountain roads, bad enough in the old diligence days, are nerve-shattering at the pace taken by the French chauffeur; and, worst of all for the entomologist, except when going slow uphill, the delight of spotting species by the roadside is destroyed; even more so of the occasional walk ahead with net or pill boxes by footpath short cuts, while the horses-toil round the dusty zigzags. It was really quite a relief when, on one occasion at least, 1 found the motor, for want of passengers, superseded by the decayed and decrepit diligence, otherwise consigned to indefinite stivation. But against these drawbacks may be reckoned the rapidity of the journey. Localities formerly reached in a day’s drive are now but a few hours distant. While the completion of the Annot tunnel on the Digne-Nice line has at length united by rail and motor the Basses-Alpes and the Alpes-Maritimes. In the ‘‘fifties”’ it took Bellier and Guillemot two days and two nights in the diligence from Grenoble to Larche. The journey, with intervals, now occupies barely twelve hours. The Vercors may be reached either from Valence or Grenoble, the usual starting point being Pont-en-Royans ; but wishing to explore the Lans valley, as well as to see something on foot of the Gorges of the Bourne, to which the road leads through 10 THE ENTOMOLOGIST. Villars, I chose the longer route. From Sassenage the road is all up-hill, with steep gradients, and, as the motor slowed down, I was able to see something of the larger butterflies at all events on the flowery banks and rocky promontories through which we wound. ‘The morning was fine; the sun full on the slopes below the Gorge d’Engins, and butterflies were in force with Satyrus cordula (males) in the ascendant, and very soon the familar Hrebia stygne. Occasional Parnassius apollo sailed lazily down the gullies, and the “‘ blues’’ were represented by Plebewus argus (egon). Aporia crategi swung from the ox-eyed-daisy- heads as we topped the Gorge and entered on the long, green, highly cultivated valley of the Lans, and there even the ‘‘ whites’ became scarce until we reached the charming little country-house Hotel du Pare, where I put up for a couple of days; nor should I have pressed on so soon had not the weather, from warm and sunny, changed suddenly to cool, with much cloud hanging low upon the hills I had hoped to climb. Flying down the road on the afternoon of the 2nd I saw one freshly emerged Papilio machaon—the only one of its kind met with until the very end of July—while a stroll towards the Gorges of the Bourne brought me to much promising ground, the waste places gay with the flowers of a fine red thistle-like Centaurea, usually most attractive to my game. The next day, therefore, I walked down the Gorge, which is singularly beautiful with its forest and rushing stream, as far as the bridge where the road divides, that to the left towards St. Martin-en-Vercors, that to the right towards Pont-en-Royans. The weather was all against collecting, but before mid-day there were fitful gleams of sunshine, and at one or two points by the roadside butterflies were flying, but difficult to reach owing to the extreme steepness of the slopes, which, by the way, were rosy with an abundance of ripe alpine strawberries. Hrebia stygne was the commonest insect with A. crategi, and on one small patch, full of wild balsams not yet in flower, Huchloe cardamines and the spring form of Pieris napi were surprisingly fresh, in contrast to Brenthis euphrosyne and Pararge hiera, both of which species had seen their best days; a small dark race of P. mera evidently just emerging. One fresh male, Melitea dictynna, was put up among some raspberry bushes, where M. athalia also occurred singly. Aglais urtice and Pyrameis cardui showed the hibernators and their progeny overlapping. The Lycznids were Polyommatus icarus and (one) Lycena arion. But it was now so cold and the wind so high that I had to give up collecting; the only other butterflies observed being Thymelicus flavus (thawmas), Chrysophanus dorilis var. subalpina, and one male C. virgauree picked up crushed on the gravel path in front of the hotel. July 4th was equally windy and cool—fine without sun—and the mountains still canopied with A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 11 cloud, so that I had little hope of achieving much in the way of a bag on the path to the Col Vert—a mountain walk decidedly reminiscent of the green unproductive Plombs of Cantal, de- scribed by me in the ‘ Entomologist’ (vol. xli. p. 266), the similarity being heightened by the clumps of golden Genista sagittalis—a food-plant by the way of Nomiades cyllarus, as. M. Rehfous tells us.* ‘The presence of innumerable herds also warned me of what I might expect, and the few butterflies met with, chiefly Canonympha pamphilus and Cupido minimus, were actually kicked out of the herbage. Waking next morning to the same depressing weather conditions, I took advantage of the motor for Pont-en-Royans, which makes the tour of the Gorges, and after an interesting and exciting journey found the sun shining brightly upon the most picturesque of riverside towns. Thence the road mounts by the Petits Goulets to the Grands Goulets, and on to Baraques, where I spent the rest of this and the succeeding day with decidedly better results. Here there is plenty of excellent collecting ground towards the northern entrance to the Gorges, as well as between Baraques and La Chapelle*en-Vercors, whither I was bound; and I only regret that time prevented my making a longer stay, and that I had not been able to include Pont-en-Royans itself in the plan of campaign. Agriades corydon males were flying on the dusty road outside Pont-en-Royans, and Parnassius apollo was soon in evidence; S. cordula and E. stygne common at the gates of the Grands Goulets in the Vallée d’Hchevis on the 5th and most of the 6th under a hot sun. Both Thecla ilicis and T’. spint pervaded the low sloe-bushes, with decidedly passées P. podalirius females evidently ovipositing, and rather worn occasional Limenitis camilla. Ccenonympha arcania, Aphantopus hyperanthus, Pararge megera, and Melanargia galatea, were all common and fresh ; the first perfect males of Satyrus hermione basked on the warm rocks and feasted upon the usual dainties ! Brilhant G. rhamni affected the same small coppices by the roadside, and a large tawny-winged butterfly which flew into my net proved to be a newly emerged male Hugonia polychloros. An even better terrain for butterflies, however, lies about a mile and a half out of Baraques on the road to La Chapelle, my next objective. At this point the mountains descend in easy slopes to the road, and there is an abundance of shrub and flora; the same red Centaurea, as before mentioned, again proving a most effective lure for many species. Following a cart track up the hill I was soon at work on what should have been a most productive locality if only the sun had obliged. The afternoon was far advanced before it came out at all strongly, and then nearly everything had gone to roost. The morning of the 7th *« * Bull. Soe. Lépid. Genéve,’ vol. ii. fase. 4, p. 241. 12 THE ENTOMOLOGIST. did however yield an hour or two of warmth, and whenever the sun broke through for a minute or two butterflies became tantalisingly profuse. Iwas especially anxious to investigate the Hesperiids of Drome, but though I worked hard at this point and quartered every acre of the likely-looking ground, I only succeeded in netting one of the elusive Black-and-White Skippers which whizzed past me at long intervals, but seemed never to rest upon the wing and to disappear like magic the moment the light failed. This one example is of considerable interest all the same. It is a splendid male Hesperia alveus—a true moun- tain species as we now know, and entirely different from H. armoricanus, the “‘ alveus’’ of the plains as heretofore supposed. The coloration of the under side is also quite different to that of my Pyrenean and Swiss Alpine examples, the ground tint being deep rich green and not yellow- or olive-green, in this respect resembling a single example of the same species taken by me last year at Herkulesbad. Another surprise was the first Colias captured—C. phicomone—a male, the largest I have seen; and this at the lowest altitude I ever encountered the species—about 3000 ft. (Mr. Wheeler places the range in the Central Alps from 4000 ft. to 8000 ft., but mentions one even lower record, 2240 ft., Oberstalden (Frey) ). Of the Lycenids, Polyommatus hylas was the most distinguished—a few males—and Aricia medon (astrarche) the commonest; and the latter, if not actually abundant, at least flying together in some quantity. Plebeius argus raales were also well to the fore, and there were plenty of Lycena arion males flitting with M. galatea over a little patch of wheat at the foot of the slopes, the blades swaying in the wind seeming also to have a peculiar fascination for P. apollo as it made a regular up-and-down hill flight. C. hyale, very swift on the wing, was common. But before noon the clouds were up, and the night at La Chapelle-en-Vercors, in the cleanest of little inns, so cold and grey, that I was again on the road south at five in the morning, bound for the Col de Rousset in the voiture publique which here, at all events, has not been snuffed out by the motor. At this time of day, with a dour sky and keen wind blowing, the road from La Chapelle to La Britiéere and Rousset at the foot of the Col seemed uninviting. From the latter village, however, the road becomes decidedly interesting, and with sun and blue sky later in the day would no doubt be productive, though it is still quite northern in character— forest-trees and flora alike. Finally, plunging into a long tunnel, we emerged at the Refuge just below the actual summit of the Col de Rousset, and at a step we had passed from the cool beech forests and pallid verdure of the north to the true Midi of barren lavender- haunted mountains, and aromatic wastes presently animated with the myriad insect-life that moves and has its being under A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 13 the gracious influence of the sun. Above, a mist still hung over the topmost cairn surmounting the tunnel. Three thousand feet below lay Die glittering in the sun, and the sound of the bells of the incoming diligence, mingling with those of the herds on the dewy hill-pastures, was borne upwards with the wind of the morning which is the breath of Provence. An hour or so, with hot coffee and rolls, in the still chilly *‘ cazebo’’ of the Refuge, and the sun was on the Col itself, and presently, as we moved downwards, the limestone ravines be- came alive with Hrebia stygne, Parnassius apollo, and Satyrus cordula, Argynnis adippe, Issoria lathonia, S. alcyone; and in the lavender region ‘‘ Blues” battling with the strong wind which now blew up thick clouds of dust until we were all as white as any Pierid of them all. Lower down, where the lavender and wild-thyme were in full blossom, Colzas edusa put in an appear- ance ; and I noted the first Chrysophanus alciphron var. gordius males, gleaming like jewels on the purple spikes of bloom with azure A, thetis, P. hylas and A. escheri, the richly-purpled “Blue” flying with them, being no, doubt that latest of rediscovered Lycenids, Agriades thersites, though I did not recognize it at the time. [ had hardly reached Die railway station, however, when a whirlwind of dust, precursor of a thunder shower, of exceptional violeace enveloped me ; and grate- ful, indeed, was the rain upon the parched Avenue du Chemin de Fer, as I endured it for a half hour in a fly-haunted, frowsy restaurant, before the train—the slowest ‘“‘omnibus”’ surely that ever crept—bore me away to Veynes, and late in a warm night, now ‘‘ full of stars,” to Digne of many pleasant memories, entomological and otherwise. List or RHOPALOCERA TAKEN AND OBSERVED AT VILLARS-DE- Lans (IshrE), aND IN THE VeERcorS (Droéme):—G. G.=Grands Goulets. G.B.= Gorges dela Bourne. La Ch. = La Chapelle- en-Vercors.—Hesperia alveus, La Ch.; Augiades sylvanus ; Thymelicus lineola, T. flavus; Chrysophanus dorilis. var. sub- alpina, G.B.; C. virgauree, Villard, C. alciphron var. gordius, above Die; Lycena arion, La Ch., G. B.; Cupido minimus, Villard, La Ch.; Aricia medon, G. B., La Ch.; Polyommatus icarus, P. hylas, La Ch.; Agriades escheri, above Die; A. corydon, Pont-en-Royans, A. thetis, and probably A. thersites, south side Col de Rousset; Plebeius argus, G. B., La Ch.; Celastrina argiolus, La Ch.; Thecla ilicis, T. spini, G. G., La Ch.; Papilio poda- lirius, G. G., P. machaon, Villard; Parnassius apollo, above Pont-en-Royans, G. G., LaCh., Col de Rousset; Aporia crategi; Pieris brassice, P. rape, P. napi, G. B.; Huchloé cardamines, G. B.; Leptidia sinapis, Colias phicomone, La Ch.; C. hyale, C. edusa, Col de Rousset ; Gonepteryx rhamni, G.G., La Ch. ; Pyrameis atalanta, P. cardui ; Vanessa io, La Ch.; Aglais urtice, Eugonia polychloros, G. G.; Pararge mera, P. hiera, G. B., 14 THE ENTOMOLOGIST. P. megera; Satyrus hermione, G. G., La Ch., S. uleyone, Col de Rousset, S. cordula, above Grenoble, Pont-en-Royans, G. G., La Ch., Col de Rousset; Hpinephele jurtina, E. tithonus, La Ch.; Aphantopus hyperanthus, G. G., La Ch.; Canonympha arcania, C. pamphilus ; Hrebia stygne, Gorge d’Engins, G. G., G. B., Col de Rousset ; Melanargia galatea. (To be continued.) SOME NOTES ON THE LEPIDOPTERA OF LA SAINTE BAUME, VAR, 8S. FRANCE. By Rev. F. E. Lows, M.A., F.E.S. I. Burrerruizs. WE spent part of our two last summers at La Sainte Baume in Provence, a neighbourhood little explored, I think, by English collectors. Our experience extended from June 24th to July 2nd in 1912, and from June 21st to July 5th in 1918. Asa hunting-ground it proved a most interesting locality to the lepidopterist, both for butterflies and, more particularly perhaps, for moths. The range of mountains known as La Chaine de la Sainte Baume attains an average height of 2000 ft., and forms a bow- shaped ridge running nearly parallel with the Mediterranean. To the west the range terminates in the bold perpendicular mass of limestone known as the Pic de Bretagne (8129 ft.), just within the Department of Bouches-du-Rhone. From thence the moun- tains, with a slight curve to the north-east, run across the Department of Var, and come to a fine climax in the Pointe des Beguines (3362 ft.). After this the ridge rapidly declines in height, and merges in the generally hilly surface of this part of Provence. The north part of the chain, on which is the famous Grotto, from which the mountains take their name, is precipitous, making almost a straight line against the sky between its two extreme points. All the lower half of this side is clothed with what is claimed to be virgin forest. It contains few really fine trees ; but is exceptional in character for these regions. At the foot of the mountains extends the tableland known as the Plateau du Plan d’Aups, some 1800 ft. above sea-level. Here, immedi- ately under the Grotto, is the Hotellerie de la Sainte Baume, our headquarters. The Hotellerie deserves a few words to itself, both on account of the kindness of our host and hostess and also owing to its history. The building was originally a religious house in charge of the Dominicans, who were dispossessed by the Government in 1904. It was purchased by its present owners, largely with a LEPIDOPTERA OF LA SAINTE BAUME, VAR, S. FRANCE. 15 motive of preserving its religious uses. And to those to whom it appeals, there is an extraordinary charm in the devotional atmosphere surrounding the place. For centuries it has been a sacred spot to the warm-hearted and highly imaginative Provencals. The centre of this feeling is a Grotto three-quarters of an hour walk above the Hotellerie, in which, according to tradi- tion, St. Mary Magdalene spent the last thirty-three years of her life in penitential devotions. This large cave has been transformed into a spacious church. At the back is a narrow natural plat- form in the rock, upon which the Saint is said to have performed her devotions, called Le Rocher de la Pénitence. Below is a . reclining figure in marble of the Magdalene, a gift of the famous Mgr. Dupanloup. The Grotto has for centuries attracted annu- ally great numbers of pilgrims, among whom have been both Popes and Kings. It is still in the present day the most highly esteemed goal of Provencal devotees. There is a beautiful little modern chapel in the Hotellerie, containing some good mural paintings. Here Mass is celebrated every morning, and all the staff and many of the visitors attend. The Plateau du Plan d’Aups is reached by carriage and good roads, ascending in the usual sweeps and zigzags, either from Aubagne vid Gémenos on the west, or vid Nans from St. Maxmin on the east. There is also another way from Auriol, joining the Gémenos road outside the village of Plan d’Aups. The plateau itself, of curious geological formation, is a stony, arid plain, covered with stunted vegetation and a few small isolated fir trees; flowers, at least at midsummer, are few. The mountains of Sainte Baume wall it in on the south side, and corresponding hills of less altitude, and more irregular, on the north; at the east and west are deep valleys, through which the above roads descend. The north side of the plateau is curiously seared by irregular ridges of rock running from east to west, about which is a considerable growth of broom and scrub, often concealing dangerous holes and fissures between the up- standing rock. All this is good ground for “‘ Hairstreaks,” and ** Blues ” especially. On the first two days the wind rather interfered with collect- ing, afterwards the weather was perfect. On June 22nd, there- fore, I confined my work to the north side of the plateau where the shrubs and rocks afforded some shelter, and there were many warm corners. One of my first captures was an excessively small female Chrysophanus alciphron var. gordius. This insect, I fancy, is very far from common in this neighbourhood. I only took one other this year; that also a female. But their condi- tion did not in the least suggest that the species was over. Last year I only took one male. C. phleas, the only other “‘ Copper” seen, was also quite a rarity. Perhaps later broods would be more abundant. At this date Thecla spini was just 16 THE ENTOMOLOGIST. emerging, but became very common later. The specimens were not so largeas those I have taken at Digne and La Granja; more like the Rhone valley (Swiss) examples, but with the white line and blue spot on the under side more pronounced. Thecla ilicis, abundant, was generally worn; and var. esculi perhaps commoner still, but I did not find 7. tlicis var. cerri. Of T. acacie I was able to secure a few in fine condition and of large size; still it was very scarce, and considerably more alert than its congeners. One is accustomed to see Plebeius argus (egon) very abundant at times, but never have I seen anything like the multitude of this little ‘‘ Blue” extending over so wide an area. They fly in numbers over the whole plateau, and hang from every grass stem. The males were all of the form we expect in the south, with shining silvery white under sides. The females showed some variety. They were pretty evenly divided between all brown forms, and others suffused in various degrees with blue, but in many cases in both forms there is a very fine but strongly defined white line on the upper side hind wing just before the fringe. I sent one or two of these to Mr. Wheeler for inspection ; who writes: ‘‘ The white line on the upper side hind wing is very remarkable. I have only noticed it hitherto in medon, and it is hardly so marked in any specimens I have ever seen, even of that species.’ Of course, one effect of the white line is to throw up the orange chevrons into greater prominence. The orange in most cases (though not always) is continuous on both wings almost to the costa of the fore wing. In one beautiful brown specimen there is a series of small, but very distinct, blue spots on the inner side of the orange marks, on the upper side hind wing, faintly suggesting the marking of Orion var. ornata. One other male aberration is destitute of all spots on the under side of fore wings, including the discoidal, except the outer row, thereby outdoing Icarus var. icarinus; and in the lower wings the three spots nearest the anal-angle are long and elongated. The next day I turned my steps towards the woods on the east, especially one protected by a notice ‘“‘ Chasse Gardée ’— which I took not to exclude a butterfly net. Here I saw the first of a coming shower of Gonepteryx cleopatra, a male. Last year, by the way, I was rather surprised to see several females two or three days before a male appeared. Melanargia syllius had been not uncommon, but was much worn. The best thing was Leosopis roboris which appeared in increasing numbers during our stay. I saw no ash at Sainte Baume; evidently the food- plant here is oak; some German authors give also privet, and even elder. The specimens were finer than those of Digne, and the species much more abundant. Brenthis hecate also began to show itself on the edge of the wood, and B. dia was of exceptionally large size. I also got a very nice banded male of Melitea athaha. All the athalia were dark, and very strongly LEPIDOPTERA OF LA SAINTE BAUME, VAR, S. FRANCE. 17 marked. M. parthenie was in its last stage of tattered garments. On the 24th Limenitis camilla was not infrequent on the road descending to Nans, and G. cleopatra (females) and Satyrus alcyone first appeared. On June 25th I made across the plateau in the opposite direction to climb the Col de Bretagne. I afterwards found that there is a much better path and much better sport by the forest under the mountains. All the way insects were most abundant. In one or two openings, or little meadows, which slope southwards from the edge of the wood to the plateau, I saw, I think, a greater number of butterflies than I have ever seen in an equal space—not excepting Swiss locali- ties. LL. camilla was specially noticeable. I have often seen L. sybilla in flocks, but never before camilla, though the latter is, I should say, a more widely distributed species. At the top of the Col, just under the perpendicular mass of the Pic de Bretagne, Polyommatus escheri was well represented by strikingly fine specimens of both sexes. One female shot with blue was the first I have seen of this form. I sent it to Mr. Wheeler, who informs me that ‘“‘ this slightly blue form of female escheri is stated by Turati to be cominon in the Alpes Maritimes.” Mr. Wheeler further says that there is another form about as blue as corydon ab. semisyngrapha; this has been named subapennina by Turati, and is not very scarce on the lower slopes of the Apennines; and that he himself has taken one such at Fiesole, which he exhibited before the Entomological Society, London, in 1909. These, I suppose, are comparatively newly noted varieties, as I find no allusion to any blue forms of the female either in Staudinger, Ruhl, Wheeler, or the new editions of Spuler’s or Berge’s ‘Huropean Butterflies.* P. eschert was to be taken all over the district, but it was on the Col that it evinced the greatest beauty of form. In this walk Pyrameis cardui was often to be seen, six and eight at a time. Agriades thetis (bellargus ? adonis?) was also there, both worn and in good order. The males generally large and of a deep blue, rather of the lilac tone of colour, and frequent among them ab. puncta, Tutt. Last year I had taken a very beautiful male hybrid, polonus, and hoped, but in vain, to renew my good fortune this year. A few ragged icarus were to be seen, and a * The Polyommatus escheri of the Bouches du Rhéne has a special form, and, though not so large as Andalusian examples, is generally larger than those found on the Central Alps. M. Oberthiir makes special mention of the female form (Lépid. Comparée, fase. iv. p. 214), to which he has given the name var. fouwlquieri, after M. Gédéon Foulquier, of Marseilles, who, with Dr. Siepi, has done so much to introduce lepidopterists to the fauna of this interesting region. I do not think either of them report the form analogous to syngrapha; but the “ slightly blue” form is not uncommon in the hill districts of the south-east. I have myself taken it at Nyons (Dréme), Allos (Basses-Alpes), and St. Martin-Vésubie (Alpes-Maritimes) ; and, in the words of M. Oberthiir, these, like var. fowlquiert, “ montrent prés du corps, des atomes bleus.”—(H. R.-B.). ENTOM.—JANUARY, 1914. Cc 18 THE ENTOMOLOGIST. new brood began to appear before we left, but I should say the species was not very abundant. The same remarks apply to Cupido minimus and Nomiades semiargus ; while of Aricia medon (astrarche) I saw but one, freshly emerged, near Nans at the end of my visit. While writing of the ‘‘ Blues’’ I will here make a leap of a few days. On June 380th we moved down to the Hotel de Lorges, near old Nans, at the foot of the road ascending to the plateau of Plan d’Aups. This hotel is some 800 ft. lower down than the Hotellerie. Late in the afternoon my wife and I, after having taken rooms and arranged our baggage, went for a short stroll. She called my attention to what she thought to be a strange form of corydon at rest. I caught it and pill-boxed it, but could only see the under side, which looked like a somewhat unusual P. meleager. When killed it proved to be a typical male Dolus. Of course on the next day we were on the look-out for more, but it was not until two days later that it turned up again, and then not on the same ground. The first specimen was taken on the rocky sides of the hill upon which the ruined chateau stands, but the rest were taken in the clearings of the wood and edges of fields skirting the wood. On July 6th I got six males and four females, and Mrs. Lowe two of each sex. In this locality Dolus presents the double interest of affording specimens both of the type and of var. vittata, usually assigned solely to the Department of Lozére. I left before the species was fully out, but my captures show of the type eleven males and seven females, against five males and one female var. vittata. It must be noted, however, that some of these reckoned of the type form have a decided tendency to the streak on the upper side hind wing which distinguishes the variety. They might be called var. intermedia. This is particularly true of Certain of the males. All former specimens in my cabinet came from Florac and Mende, the gifts of Mr. Jones and Mr. Rowland-Brown, and are of course var. vittata. On comparing these with this year’s catch at Nans, it is at once evident that the Nans specimens are on an average considerably larger than those from the Mende district—a much darker blue, and also have a very much broader black edge to the wings. It is quite easy to pick out a Nans specimen if you mix them together. Agriades corydon began to appear on July 2nd at Nans, and came out very slowly—the males with rather dark and sharply defined margin; the females did not show up before we left. I took one very beautiful example of var. cinnus. One fine female, Libythea celtis, was taken between Nans and Sainte Baume off flowers of bramble. But I never saw another, neither could I see any plants of Celtis australis. At Sainte Baume Satyrus alcyone had appeared on June 24th; at Nans, LEPIDOPTERA OF LA SAINTE BAUME, VAR, S. FRANCE. 19 S. hermione came to hand with wings hardly dry on June 30th. Of the Argynnids Brenthis hecate was fairly common and widely distributed. B. dia passing, but had been remarkably fine and very common. Of the big brotherhood, Argynnis niobe var. eris, was the first to be seen, and not common; next A. adippe and A. aglaia; and, lastly, Dryas paphia; these would all be doubtless common later. The little Canonympha dorus was very local, and never abundant; C. arcania not in great numbers. C. pamphilus gave me several nice forms, two var. bipupillata, one fine ab. thersites, and, lastly, a beautiful female, in which the round spot towards the apex of fore wings is of enormous size, with white pupil on under side 3 mm. in diameter, or the exact size of the letter O in Queen Victoria’s name on a florin of 1890. This aberration I have decided to call glawcopis, until I hear that it has been named before. Before leaving on July 5th I had an hour or so in the immediate neighbourhood of our hotel, and was lucky enough to take a very perfect aberration of Melitea didyma (female). These things are difficult to describe, and one is very conscious of M. Oberthur’s reasons for demanding a figure of all named varieties. The striking feature of this specimen is the wide expanse of clear colour on the disk of all wings, devoid of the usual black markings. It is yellow of the lightest occidentalis forms, and the fore wings have no central markings whatever between the single sharp zigzag black edge of the fringe and two basal spots, which are open rings; above these, next the costa, are two open marks which form the figure 30. The lower wings are of the same ground colour as the upper, and all black marks are gathered together in a central band formed by wedge-shaped dashes. On the under side the primaries, which are of a darker reddish tint than on the upper side, are traversed by a central band of seven black dashes. The secondaries, of a pale cold yellow, have the central light band strongly defined between rows of large black spots, after which the wing is self-coloured up to the black line before the fringe. I have given to this, in honour of the locality, the name ab. magdalena. The following is the complete list of butterflies from Sainte Baume district noted by me, seventy-four in all, exclusive of varieties. PaPILIoNIDH.—Papilio podalirius, P. machaon. PIERIDE.—Aporia crategi ; Pieris brassicae, P. rape, P. napi ; Euchloe belia var. ausonia (one); Leptidia sinapis, scarce ; Colias edusa and var. pallida (one), C. hyale, scarce; Gonepteryx rhammi, G. cleopatra. NympHALIDE. — Limenitis camilla; Pyrameis atalanta, P. cardui; Hugonia polychloros; Polygonia c-album; Huvanessa c 2 20 THE ENTOMOLOGIST. antiopa ; Melitea phabe, M. cinxia (one), M. didyma, M. athalia, M. parthenie ; Argynnis niobe var. eris, A. aglaia, A. adippe ; Dryas paphia; Brenthis hecate, B. dia, B. euphrosyne (one worn). Satyripm.—Pararge egeria var. intermedia, P. mera, P. megera; Satyrus hermione, S. alecyone, S. circe ; Hipparchia semele; Epinephele jurtina, E. pasiphe; Canonympha pamphilus and vars. C. dorus, C. arcania; Melanargia syllius, M. galathea var. procida. LisytHeipm.—Libythea celtis. Lycmnipm.—Chrysophanus alciphron var. gordius; C. phleas and var. eleus-ceruleopunctata; Cupido minimus; Nomiades semiargus ; Polyommatus dolus and var. vittata, P. hylas, P. escheri, P. icarus ; Agriades thetis and hyb. polonus, A. corydon and ab. cinnus; Aricia medon; Plebeius argus; Celastrina argiolus ; Leosopis roboris; Thecla spini, T. ihcis, T. escult, T. acacia ; Callophrys rubt; Zephyrus quercus. Hesreripm.—LHrynnis aleee (one); Hesperia cartham, H. alveus var.?*; Pyrgus sao; Thymelicus acteon common, 1’. lineola, T’. flavus ; Pamphilus sylvanus. NOTE ON THE OVIPOSITION OF RHYSSA. By L. N. G. Ramsay, M.A., B.Sc. Tue remarkable insects of the genus Rhyssa have for long been known to prey on the wood-boring larve of Siricide, introducing their eggs into the tunnels of the latter by means of their enormously elongated ovipositor. The ovipositor is some- times even found sticking ina Sirex-infested log (as, for example, the specimens exhibited in the insect gallery at South Kensington), but, I understand, the manner in which the insect contrives to insert this unwieldy appliance into the tree-trunk has not hitherto been fully described. I hope, therefore, that the following account may be of interest to entomologists. The event described was witnessed in the summer of 1909, while I was staying in the southern part of the Black Forest, to the west of the Wehratal. On the afternoon of August 29th, while skirting a wood—the very finest conifers of the Black Forest flourish in this locality—I happened to pause beside a pile of small pine-logs, and as I stood there one of these extraordinary insects appeared and settled on one of the logs. I will quote verbatim from my notes written the same day :—“‘ It sat still for some time, and then began to walk about, feeling every hole and * Probably H. belliert var. fowlquiert.—(H. R.-B.) NOTE ON THE OVIPOSITION OF RHYSSA. ea | corner in the rough bark with its long antenne. After a minute or two of this it stopped, and drew up its long body, doubling the long black ovipositor underneath itself; it had to hitch itself up - several times before it got the long needle into position under- neath, with the tip in a crevice. Then it gripped the bark with its claws and gradually thrust the ovipositor about half an inch into the bark, then suddenly flew away, perhaps because it completed laying the eggs, perhaps because I had gone too Glose.s aye: ie Immediately after, I made the rough sketches of the beast which accompany this note. These are probably a little larger than life, although the insect was a very large one. I noted that the abdomen was black and white, the legs pale, and the antenne black. EXPLANATION OF FicureEs (diagrammatic).—1. The insect reconnoitring the bark with its antenne. 2. Getting the ovipositor into position. 3. The insect just before flying away; the ovipositor thrust home in a crevice. (Sketched from life.) At the time I was unaware of the insect’s identity, but on seeing the specimens of Rhyssa exhibited at the Natural History Museum this year, I at once recognised my old acquaintance, and comparison of the other species of the genus in the cabinet collections there leaves little, if any, doubt that this was R. persuasoria. The figures will help to indicate the manner in which the insect succeeded in bringing its unwieldy ovipositor to bear on the log. As mentioned above, these were drawn before I left the spot (with the exception of the second, which I have added now to make the action clearer), and they are reproduced without any change from my original rough drawings. As the insect 99, THE ENTOMOLOGIST. had already taken its departure, they are necessarily crude, as it was the only example of its kind on which I had ever set eyes. For this and for their obvious artistic defects I shall make no further apology, as they are merely intended to convey the manner in which the insect accomplished its object. Sharp* figures (after Riley) the allied genus Thalessa in the act of oviposition, and states that in both these genera the ovipositor “‘is brought into use by being bent on itself over the back of the insect, so as to bring the tip vertically down on to the wood, through which it is then forced by a series of efforts ; the sheaths do not enter the wood.” It is evident that this description does not tally with the foregoing observations on Rhyssa. The insect figured by Sharp follows his statements in having its long ovipositor bent on itself, out ofits normal and approximately straight form, into an almost complete circle. From purely physical considerations, is it not a little difficult to understand how a non-muscular structure could be curved at will in this way? The possibility suggests itself to the present writer that the insect there figured, after having inserted its ovipositor in the manner described in this note for Rhyssa, may have pivoted its body through an angle of 180° around the flexible fixed ovipositor, in its efforts to thrust the latter into an unusually resistant piece of wood. This might easily happen through the insect’s shifting its feet again and again to obtain a better purchase, and would explain the whole matter very simply, as the ovipositor in such a case would naturally assume the position figured. [There can be no doubt at all that Mr. Ramsay’s notes refer to R. persuasoria, L., which has an extremely wide distribution through Europe to Canada and the United States in the West, and the Himalayas in the Hast, since it is to the best of my knowledge the only species attacking pinetophagous larve. R. approximator, Fab., is said by Holmgren to attack Xyphydria prolongata, which feeds in oak; and there are several interesting accounts of the American species’ economy (Canad. Entom. xi. 1879, p. 15, &c.) and Harrington has (I. c. xix. p. 206) put on record ‘“‘ The Nuptials of Thalessa.” Myr. Ramsay appears to take it for granted that these insects bore for themselves an egg- passage through the solid wood; but it is by no means proved that they do not oftener introduce them along the tunnel of the host larva (cf. Morl. Ichn. Brit. iii. p. 25, et Revision Ichn. Brit. Mus. u. p. 10).—Ciaupr Morty. | * ‘Cambridge Natural History, Insects,’ pt. i. p. 554, 1895. 23 A MONOGRAPH or tHe Genus OSPRHYNCHOTUS, Srinoua. Family IconzEumonip#: Subfamily Cryprinm: Tribe Crypripes. By CraupEe Mortey, F.Z.S., &e. THis genus has been twice excellently described; in the first place, by Spinola (Magaz. de Zool. x1. 1841, p. 45), and later, in ignorance of any previous knowledge of it, by de Saussure (Distant’s ‘ Naturalist in the Transvaal,’ 1892, p. 229, under the name Distantella), though neither author assigned it a very definite classified position. That it is distinct from Acroricnus, Ratz. (= Linoceras, Tasch.), I am able to state from an examination of the typical species of both genera; Dalla Torre treated Ratzeburg’s genus as synonymous, but Schmiedek- necht in 1904 correctly tabulated the palearctic kinds under Acroricnus, which differs from Osprhynchotus in possessing two strong metanotal transcarine in place of only a subbasal one, in having the hind tibiz normal and not incrassate throughout, in its lack of central setz beneath the hind onychii, in its less ‘compressed abdomen, posteriorly broader head with less excavate frons, in its centrally intercepted nervellus ; but most especially in having the mouth parts but slightly produced, whereas in true Osprhynchotus species they are rostriform, with both cheeks and clypeus no shorter than the face, surmounted by strongly exserted labrum and ligula, extending in all to three and a half millimetres below the scrobes in the typical species. ‘*Osprynchotus’”’ peronatus, Cam. (Kntom. 1902, p. 182; placed in ** Linnoceras”’ by its author at ‘ Spolia Zeylanica,’ 1905, p. 97) is an Acroricnus and very common in India, whence I have seen it from the Khasi Hills, Simla, Labatach, Sikkim, Shillong, and the Kangra Valley. I may be permitted to here bring forward the unknown female of Acroricnus syriacus, Mocs. (Magy. Akad. Term. Ertek. xii. P. 11, 1888, p. 12, male), which differs from the male in little but its terebra, and this is as long as the abdomen, excepting the petiole; it is a true member of that genus and was captured by Hscalera during 1900 at Kuh Sefid in south-west Persia. The large size and nigrescent or brunneous wings of Osprhynchotus render it one of the most conspicuous genera of the Ichneumonide. That considerable confusion has existed concerning the synonymy of the species is owing to the fact that Brullé, in my opinion, described an extremely rare one in 1846, and that Tosquinet mistook it for the commonest in 1896. W. A. Schulz’s remarks upon this genus (Zool. Annalen, 1911, pp. 35-87), all the species of which he there wishes to regard as synonymous, appear to have been based upon insufficient material; he professes to have seen five examples of my last species, thirteen of my first, and an unrecorded number united under my second to fourth. Among these he failed to 24 THE ENTOMOLOGIST. discover any plastic distinctions sufficient to justify specific rank (though I consider the difference in shape of the areolet and brachial cell to be constant), and thinks the “distribution of red-brown colour varies greatly, apparently according to in- dividual developement”; to me this variation appears very slight, and that of the hind tibial colour even less so. The synonymy of the whole genus is repeated in the same critic’s “‘ Zweihundert alte Hymenopteren”’ (Berl. Ent. Zeit. 1912, p. 68), where O. violator, Thunb., alone is allowed to stand, though far antedated by O. objurgator, Fab., as I pointed out in 1909. TABLE OF SPECIES. (8). 1. Wings, basal abdominal segment and part of thorax black. (3). 2. Areolet externally subrectangular above ; bra- chial cell apically less explanate; anus pale; flagellar pale band usually six-jointed . 1. violator, Thunb. (2). 3. Areolet externally rounded above; brachial cell apically strongly explanate; anus black; flagellar pale band usually four-jointed. 4. Propleurz and temples utterly glabrous; hind tibize white only to their centre . . 2. objurgator, Fab. 5. Propleurz striate and temples pilose; central hind tibial flavous band extending far beyond centre. 6. Hind tibial black band longer than calearia: length 27 mm. : k 3 ; . 3. gigas, Kriech. (6). 7. Hind tibial black band not longer; length 21 mm. . . 4. ruficeps, Cam. 8 9 (1). 8. Wings brown, basal abdominal segment and nearly whole thorax red. (10). 9. Wings basally paler; flagellum and hind legs red and not pale banded . O. pulcherrimus, Kirby. (9). 10. Wings unicolorous; flagellum and hind legs black, pale banded ; : 2 . 8. flavipes, Brullé. 1. OSPRHYNCHOTUS VIOLATOR, Thunb. Ichneumon violator, Thunb. Mem. Acad. Sc. Petersb. ix. 1824, p- 803; cf. Roman, Zool. Bidr. Uppsala, i. 1912, p. 288. Osprhynchotus capensis, Spin. Mag. Zool. xi. 1841, p. 75, male, female. Distantella trinotata, Sauss. Nat. Trans- vaal, 1892, p. 280, female. Maximilien Spinola beautifully figures (loc. cit. pl. Ixxv.) both sexes with details of the head and of the male abdomen, which latter is not apically pale; he regarded the genus as a ‘‘ Sous-famille des Ophionides”’ and derived his generic name from the rostriform mouth; only three examples of both sexes were known to him, from the Cape of Good Hope. I have examined what Mr. W. L. Distant assures me is the type specimen of Saussure’s elaborately described genus Distantella, and find it to be entirely synonymous with O. capensis, Spin. A MONOGRAPH OF THE GENUS OSPRHYNCHOTUS. 25 This genus has since been employed by both Cameron* and Schmiedeknecht, with the erroneous characters ascribed to it by Ashmead (Proc. U. 8. Nat. Mus. 1900, p. 41), for very different insects, whose position is consequently untenable. Though Saussure records only a single female from Pretoria, there is a long series of (presumably) cotypes from that locality in Distant’s collection, now in Mus. Brit.; the former was at a loss where to place the genus and adds, “ Je ne crois pas pouvoir le placer, ailleurs que dans la tribe des Cryptiens.”’ ‘There area score of females in Mus. Brit. found by Dr. Smith in 1844 in South Africa, in 1852 in West Africa, in 1859 at Knysna in South Africa, later at Sterkfontein, &c., in the Transvaal, Queenstown in Cape Colony, and in March, 1900, at Slievyra, in Natal. I have also seen it from Bonnefoi, in the Transvaal, in the Deutsches Entomologisches Museum of Berlin. 2. OSPRHYNCHOTUS OBJURGATOR, Fab. Ichneumon objurgator, Fab. 8. I. 1781, p. 426; Cryptus objur- gator, Fab. Piez. 1804, p.79, female. Osprynchotus heros, Schlet. Ann. Soc. Ent. Belg. 1891, p. 33, female; Tosq. l. c. 1896, p. 248, male, female. This species is described :—Head and thorax dull red and punctate; male face white; antenne black, white-banded; abdomen black, smooth and shining, apically compressed; legs black, the front ones dull red with tibiz dull stramineous, the hind tibiz and sometimes their tarsi pure white-banded ; wings infuscate-violaceous ; length, male 20 mm. and female 28 mm. All this, as I have already pointed out (Entom. 1909, p. 135), exactly agrees with the type of Fabricius’s species, which is still preserved in the Banksian Cabinet in the British Museum. This species is extremely constant in the coloration of its hind tibie, and the score in Mus. Brit. all have pure white hind tibial bands, extending only to the centre, in both sexes. Schletterer’s female was from the equator in the Congo, Fabricius’s from ‘‘ Africa equinoctiali”; Tosquinet gives it a range through Togoland, the Cameroons and Senegal, to Sierra Leone; and it appears pretty constant to that latitude, for I have seen examples only * Distantella pilosella, Cameron (Journ. Bombay Nat. Hist. Soc. 1909, p. 729) is a true Cryptws, sensu Thoms., male. Of Cameron’s other Indian species of Cryptus, C. luculentus (Entom. 1905, p. 85) = tarsolewcus, Schr. ; C. himalayensis (Tr. Ent. Soc. 1904, p. 106) = Hedycryptus—not a good genus—filicornis, Cam. (Zeits. Hym.-Dip. 1903, p. 299); C. orientalis (Manch. Mem. 1897, p. 16) = obscurus, Grav. ; C.nurset (J. Bomb. N. Hist. Soc. 1906, p. 285) = insidiator, Smith; Bwathra—not a good genus—ru/i- ventris (Tr. Ent. Soc. 1903, p. 284) must be included and is probably hardly distinct from apparitortus, Vill.; nor is C. bibulws (Tr. Ent. Soc. 1904, p- 106) from C. albatorius, Vill. Cryptus indicus, Cam. (Manch. Mem. 1897, p. 15) = Mesoleptus annulipes, Cam. (lib. cit. 1900, p. 103) = Syzeuctus annulipes, Morley, Fauna of India, Ichn. 1913, p. 286.—C. M. 26 THE ENTOMOLOGIST. from Sierra Leone in 1888 (Rev. F. D. Morgan), Sierra Leone (J. J. Simpson and W. G. Clements in 1893), Shengay in the north Sherbro District of Sierra Leone in 1910 (W. Addison), Kokona on March 26th, 1912, Gigbema on August 22nd, 1912, Bunbumbo on August 15th and 16th, 1912, and Kamagbouse on April 6th, 1912; from Nigeria at Ilorin on June 8rd, 1912, Minna during 1911 (J. W. Scott-Macfie), and on October 18th, 1910 (J. J. Simpson), Oshogbo, in southern Nigeria, in 1910 (Dr. T. F. G. Mayer) ; from the Congo in 1848 (Dr. Richardson) and 1890 (Miss Sharpe); from the Kast Neave has sent several females from the Tero Forest, near Buddu, taken at the end of September, 1911, at 8800 ft., and near Kumi and Lake Kiogo at 3500 ft. in the Uganda Protectorate during the preceding August. The Deut. Ent. Museum has it from Togo and the Cameroons. 3. OspRHYNcHoTUS GIGas, Kriech. Osprynchotus gigas, Kriech. Mem. Accad. Sc. Bologna, iv. 1894, p. 86, female. This I believe to be the commonest species of the genus. It is described :—Black; head transverse, posteriorly obliquely constricted and red with the facial orbits paler, fulvescent ; antenne black with scape red, and the eighth to twelfth joints pale fulvous; mesonotum rugosely punctate, and not at all red; metanotum rugose; scutellum somewhat convex, punctate, centrally subglabrous, with the prescutellar lateral lamine red- marked; abdomen glabrous and nitidulous, with terebra 12 mm. in length; front legs red, with infuscate tarsi; the posterior black with a band, occupying about two-thirds of the hind tibie, pale flavous; most of the apical half of the hind metatarsi, and whole of the second to fourth joints, concolorous; wings dark violaceous, with their apices broadly black; a subpellucid mark beyond the stigmal base, and three hyaline fenestre in the disco-cubital, second recurrent and outer areolar nervure; length, 27 mm. Kriechbaumer’s above account is not very accessible and was overlooked by Tosquinet; I, consequently, give it in extenso from his part of the paper ‘‘ Rassegna degl’ Imenotteri Raccolti nel Mozambico dal Cav. Fornasini.”’ I have seen a hundred and forty specimens of both sexes (the male differs in no way but its paler red capital colour) which agree exactly with this description from Abyssinia, British East Africa, Uganda, German Hast Africa, Nyassaland, Mocambique, Delagoa Bay, north and north-east Rhodesia, Natal; and a male in the Rev. T. A. Marshall’s collection which is labelled ** Senegal,” but several of his African localities were incorrect, and the present species seems rare or wanting towards the east of the Continent. I have seen both sexes in the Deut. Ent. Museum from Three Sisters, near Barberton, in the Transvaal, where they occurred during October and December. A MONOGRAPH OF THE GENUS OSPRHYNCHOTUS. 27 4, OSPRHYNCHOTUS RUFICEPS, Cam. Osprynchotus ruficeps, Cam. Ann. 8. African Mus. 1906, p. 142, female. Male and female. A black species, with flagellar band stramineous; female with head, under side of scape, and most of prothorax red; male with face, under side of scape flavous, thorax black; both sexes have the hind tibiew flavous with extreme base, and a band at their apex not longer than their calearia, black; hind tarsi flavous with a band at their base shorter than the calecaria, and onychu, black ; wings violaceous; length, 21 mm., terebra, 10 mm. I greatly doubt if this species be aught but a small and southern form of the last; Cameron did not know O. gigas, Kriech., and the present species seems separable from it only in its smaller size and narrower black hind tibial band. It was described from the Umvoti River in Natal; and I have seen a dozen examples, agreeing in the above characters, from East Karoo, in Cape Colony (A. Howarth), Port Natal, in 1856 (Mr. Plant), Howick, in Natal (J. Cregoe), the Transvaal on November 29th, 1896 (A. Ross and A. J. Cholmley, 1906), Johannesburg and Sterkfontein (H. P. Thomasset), and Pretoria (Distant). 5. OSPRHYNCHOTUS PULCHERRIMUS, Kirby. Cryptus pulcherrimus, Kirby, Bull. Liverpool Museum, iii. 1900, p. 14, and ‘The Natural History of Sokotra and Abdelkuri,’ by H. O. Forbes, 19038, p. 237. The type was taken at Homhil (one female) at 1500 ft. in Eastern Sokotra on January 23rd, 1899; and cotypes:—One female at Dahamish at 350 ft., in Sokotra, on December 24th, 1898; one female at Goahal Valley, in Eastern Sokotra, on January 16th, 1899, and one male at Thluteed at 1200 ft., in Sokotra, on January 15th, 1899. All these are in Mus. Brit. The lack of all black or red markings renders this species conspicuously distinct ; its mouth is no less rostriform than in its congeners, and I was in error (Entom. 1911, p. 212) in ascribing it to the genus Acroricnus croricnus, Ratz. 6. OsPRHYNCHOTUS FLAVIPES, Brulle. Hist. Nat. Ins. Hym. iv. 1846, p. 185, female; (?) Tosq. Mem. Soc. Ent. Belg. 1896, p. 246, male, female. This species was originally recorded from Senegal only; subsequently, Tosquinet, whose description looks like a com- pound of Brullé’s and that of O. gigas, Kriech., adds such diverse localities as Togoland, Angola, the Cape, Tanganyka, the Congo, and Scioa, but I place no reliance upon his -knowledge of the present genus. In my own experience, which is slender, this species is extremely rare, and has, I believe, been misunderstood by all subsequent authors. Schulz professes to recognize it from both Senegal and Senegambia. I have seen but a singie 28 “THE ENTOMOLOGIST. female, labelled ‘‘ Gambia” in the British Museum, which would point to a range nearly as restricted as that of the last species ; this female exactly agrees with Brullé’s description in every way, especially in the red basal segment and the terebral length of twelve millimetres, not only eight as indicated by Tosquinet. The species referred to under the present name by Col. Bingham, (Trans. Zool. Soc. xix. 1909, p. 179) from Mount Ruwenzori, is O. gigas, which was at that time mistaken for it in the National Collection. The coloration of O. flavipes is quite distinctive :— Head, thorax, scape and extreme apices of antenne rosy; the last with only two joints white; mesonotum and metanotum sometimes more or less, but never entirely, nigrescent; abdomen black, with the basal segment entirely red; legs ferrugineous with the hind femora, tibie and tarsi black, the basal half of their tibiz and second to fourth tarsal joints very pale flavous ; wings brownish, not at all nigrescent, but with violaceous reflection ; length, female, 25 mm. TWO new MYRMECOPHILOUS APHIDES rrom ALGERIA. By Frep. V. Tueosatp, M.A., F.E.S., Hon. F.R.H.S., &e. Tur two new Aphides described here were taken by Mr. P. A. Buxton and Mr. R. Gurney in ants’ nests in Algeria; one of them was also found with termites. So far only a single aphid has been recorded from the nests of white ants, namely, T'ermit- aphis circumvallata, Wasmann (Tijdschr. v. Entomol. xlv. 1902, pe 10o,) plrg, ies. Te airsCh) Professor Robert Newstead informs me that he is describing another peculiar form from termite nests in the West Indies. One of the two species described here is very marked, and this I have placed in a new genus for which I propose the name Rectinasus. The other comes in the genus Forda, although the adult female presents a somewhat different form to the other known Fordas. The ant hosts are given with the species described. Genus Recrinasus, nov. gen. Antenne of five segments, long, often over half the length of the body, rather thin, the first and second segments small, of about equal length, third and fifth long, about equal in length, fourth short, slightly longer than the second, the first and second have a short blunt spine, at the apex and base respectively. Hyes small. Proboscis long, from two-thirds the length of the body to a little longer than the body, carried at a marked angle to the body, often nearly at right angles ; acuminate, hairy. Setaceous mandibles and maxilla long. Body segmented. Cornicles absent. Legs rather . long and thin, but somewhat thicker in young forms. * This insect has since been placed in a new family. TWO NEW MYRMECOPHILOUS APHIDES FROM ALGERIA. 29 The marked characters of this genus are the antenne and the projecting long proboscis. The viviparous apterous female only known. Found in company with ants. _Rectinasus buxtoni, nov. sp. Apterous viviparous female-—Ochreous yellow to pale yellow and almost pearly white, pubescent; legs and antennze brown; proboscis black at the apex, brown to nearly the base in some, paler in others. Eyes black. Frons more or less porrected. Vertex convex to flat, broad, hairy. Antenne of five segments, the two basal ones small, of nearly equal length, the basal one somewhat the wider, the apex a. Rectinasus buxtoni, nov. sp. A. Head of apterous viviparous female; a, antenne; al, joint of first and second segments, showing spines a?; a*, apex of antenne; b, eye; c, labrum; cl, maxille ; c? and c3, mandibles; d, proboscis. 5B. Variations in head a, b, and c. C. Lateral tubercle. D. Labrum, d! apex further enlarged. of the first and base of the second with a-small dark, blunt, median projecting process, pointed towards one another, third segment long, fourth short, but longer than the second, fifth as long as the third, ending in a short, blunt nail, a small round sensorium at the apex of the fourth and a peculiar shaped one at the base of the nail on the fifth ; all the segments hairy, in some the antenne are nearly as long as the proboscis, in others shorter. Proboscis carried at a marked angle to the body, bent near the base, acuminate, the apex of the last segment, which is long and thin, black, hairy; setaceous mandibles and maxille long ; labrum moderately long, porrected, base with some hairs. The proboscis varies in length, usually about two- thirds the length of the body, but may be longer. Frons often porrected. 30 THE ENTOMOLOGIST. Pronotum constricted from the rest of the body, which is oval. Abdomen with short hairs on the anterior three-fourths, longer ones behind with shorter ones between. Cauda rounded to cone- shaped, very hirsute, hairs long. Pore-like, oval, flat tubercles at the sides. Legs rather long and thin, projecting; femora wider than the tibiz, tarsi of two segments, the basal one small, all the segments with fine short hairs. Length.—1°5 to 2°3 mm. Habitat.—Lambése, Batna, EK. Algeria. Time of Capture.— April 5th, 1918. Notes.—A large number taken in ants’ nests (Pherdole palli- dula, Nyl.), under the same stone as a nest of the termite (Leucotermes lucifugus, Ross), and three specimens from nest of Bothryomyrmex meridionalis by Mr. R. Gurney at the same time. The head varies somewhat in form; in some it is convex in front, in others flat, and some appear to have a median sulcus. The relative length of the antenne and proboscis also varies; in young forms they are about the same length, in older ones the antenne are considerably shorter than the proboscis. With regard to the connection with termites there is some doubt, for Mr. Buxton sends the following from his notebook :—‘‘ Ant, Aphis and Termite all under the same stone. The termites probably not in association, but ants and aphides actually in the same nest.”’ The termite has been determined by Holmgren as Leuco- termes lucifugus, Ross. Forda rotunda, nov. sp. Apterous viviparous female-——Dull white above, much domed ; flattened below, brown, the marked segments darkened apically. Antenne less than one-fourth the length of the body, thin, of five segments, the two basal ones short, about the same length, the basal one wider than the second, third segment the longest, slightly narrower than the second, about as long as the fourth and fifth together, the last two equal, a single round sensorium near the apex of the fourth and one large one and one or two small round ones at the base of the very short, blunt nail on the fifth, the last two segments brown, the rest yellowish, all the segments with fine short hairs. Eyes small and black, projecting from the side of the head. Vertex rounded or curved, nude. Proboscis short and _ thick, reaching just past the second cox, dark at the tip, with two sub- terminal sete; setaceous mandibles and maxill# rather short, the former spirally curled; proboscis bent under the body and more or less closely applied to it. A few hairs on the posterior of the body ; cauda very hirsute, hairs curved apically; no trace of segmentation on the white domed dorsum which has the appearance of white kid ; markedly segmented on the brown venter. Legs brown, first and second pairs very short, the femora thick and nearly as long as the tibie; tarsi of two segments, the same length in the first two pair of legs; third pair of legs longer, just TWO NEW MYRMECOPHILOUS APHIDES FROM ALGERIA. 31 projecting beyond the body, femora much thicker and shorter than the tibiae; tarsi longer than in the two front pairs; the basal segment of the feet, small; tibize and tarsi hairy, hairs very fine and short. Length.—3 mm. Inmature viviparous female.-—Colour varying from pale yellow to dull brownish grey. Legs pale yellowish brown. Antennex with the last two segments pale brown; two basal segments short, about equal length, the basal one broader than the second, the third the longest, about as long as the fourth and fifth, which are equal, a sensorium on the apex of the fourth and one at the base of the short blunt nail on the fifth, with two to four smaller ones surrounding Forda rotunda, nov. sp. A. Head of mature apterous female; c, antenne; c!, further enlarged apex ; b, proboscis; b!, mandibles; b?, maxille; a, eye; al, eye further enlarged. B. Head and antenn# of immature female. D. Front tarsus. E. Proboscis. F. Lateral view of cauda. G. Hind tarsus. it, all the segments with small hairs. Eyes small and black, not so projecting as in the adult. Proboscis reaching just to the third cox, of similar form to the adult. Legs longer in proportion than the adult, well projecting from the body, otherwise similar. Cauda rounded, hairy, hairs long and curved apically. Length.—2 to 2°5 mm. Habitat— Hammam Meskoutine, EH. Algeria. Time of Capture.—April 3rd, 1913. Notes.—One mature female and four immature ones taken in ants’ nests (T’apinoma erraticum). There is no doubt that these are all one species, although the mature form looks very different, its swollen appearance, its white kid-like upper surface and flat brown venter with marked segmen- tation is very characteristic, the younger forms are more Forda- like, whilst the adult approaches a Tycheoides in appearance but the antenna are Forda-like. The hairy cauda is prominent in all. The types of both species have been placed in the National Museum at South Kensington. 32, THE ENTOMOLOGIST. THE FOSSIL ORTHOPTERA OF FLORISSANT, COLORADO. By T. D. A. CockERELL. ORTHOPTERA are uncommon in the Tertiary rocks, and usually poorly preserved, although they must have abounded in former times as now. Probably most of the species were better able to escape destruction during volcanic eruptions than smaller and more fragile insects. The Miocene shales of Floris- sant have yielded no fewer than thirty-three species, and although this must be but a small fragment of the Orthopterous fauna of that time, it is sufficient to give us some idea of the types exist- ing perhaps a million years ago. Two new species have been recently discovered by Professor Wickham, and are described below. The Forficulide are represented at Florissant by the extinct genus Labiduromma, Scudder, with no fewer than ten species. Karwigs are the only Orthoptera in the shales which can be called common. Blattide are represented by three genera still living in America, each with a single species. It is possible that the species referred to Zetobora is really an Ischnoptera, and iden- tical with the described member of that genus. The Mantide are represented by three species, referred to two genera, both believed to be extinct. Scudder has described one Phasmid, placing it in Agathemera, a neotropical genus still extant. In the Acridiide we find the apparently extinct genus Teniopodites, Ckll. of the Acridiine; three species of Gidipodine ; and three of Tryxaline. All these Acridians, whenever their generic characters can be made out, seem to belong to extinct genera. In the Locustide we have Palgorehnia, Ckll., a remark- able extinct genus referred to Phaneropterine ; a very dubious member of the Pseudophylline ; Lithymnetes, Scudd., an extinet genus placed in the Oriental and Australian group Phyllo- pharine ; a Conocephaline referred to the living genus Orcheli- mum; two Decticine, belonging to the living genera Capnobotes and Anabrus; and two species of the widely distributed Gryll- acris, of the subfamily Gryllacridine (Gryllacrine, Kirby, Scudder). As the list stands, less than a third of the species seem to belong to modern genera, and it is quite possible that if we had complete specimens of these, at least some of them would prove to be incorrectly assigned. On the other hand, it may be that some of the genera described as extinct are still living. The whole matter must stand subject to future revision, should better materials be brought to light; but we can at least say this, that the Miocene Orthoptera of Colorado were, on the THE FOSSIL ORTHOPTERA OF FLORISSANT, COLORADO. 33 whole, strikingly different from the existing fauna of that region, and were like those of warmer regions to the south. The appa- rent resemblances in some cases to the Old World fauna may possibly be deceptive, but if they are not, they fall in line with the indisputable occurrence of such Old World genera as Glossina and Halter. ACRIDIIDE. Tyrbula scuddert, n. sp. Hind leg with femur 174 mm. long, 34 wide, superior carine strongly marked ; many broad oblique brown bars, broader than the intervals between them. Tibia of same leg 182 mm. long, $ mm. wide, the hind margin with sixteen large, two medium, and four small spines, the uppermost (small) one 32 mm. from base of tibia, the first large spine 7 mm. from base; the large spines formed as in T. multispinosa, but so closely set that their bases almost touch, and the longest spines are nearly 1} mm. long; the longer spine at apex of tibia is about 1 mm. long. Tarsus 6 mm. long. Tegmen as preserved about 29 mm. long, but if complete it would probably be about 32 mm.; width about 5mm. A slight indistinct marbling, but no distinct spots or bands. Venation as indicated in Tyrbula scudderi, Cockerell. a. Tegmen. bs. Tibial spines. the figure; the costal region broadly expanded, with oblique, rarely branching veins, much as in Straplewra texana as figured by McNeill; the first subcostal branch must be very short, as it is not clearly visible, the base of the costal field being suffusedly brown without well-preserved veins; the rest of the venation shows a general resemblance to that of various Tryxalines, with the following peculiarities : radius branching about middle of tegmen, the branches continuing close together, joined by numerous cross veins, approach- ing in apical field, but diverging again, the lower branch giving off below at least three long oblique veins; media branching a little beyond the radius, the branches widely divergent, forming an open fork, but gradually approaching as they go toward margin ; cubitus simple, ultimately joining first anal. In the figure the stems of the media and radius are too close together; with a good lens they can be seen to be distinctly separate, joined by numerous small cross- veins, but the media is only half as far from the radius as it is from the cubitus. Miocene shales of Florissant, Wilson Ranch (H. F’. Wick- ham). I make the leg the type, because it shows parts which can be compared with the descriptions of Scudder’s two species of Tyrbula. The tegmen was on another piece of shale, but I ENTOM.—JANUARY, 1914. D 34 THE ENTOMOLOGIST. feel confident that it belongs to the same species. This is probably Scudder’s supposed TJ’. multispinosa from Florissant ; but the true 7’. multispinosa is a different insect, from the Kocene of Wyoming. The Wyoming species is the type of the genus, and very possibly better material of it would indicate that the Florissant insects belong to a different genus. MANTID&. Iathophotina costalis, n. sp. Tegmen, as preserved (base and apex wanting), about 18 mm. long, actual length probably 25; pallid, the veins appearing light reddish, perhaps green in life; similar to LZ. floccosa, but with the costal field much larger (nearly 2 mm. broad near middle), and the inferior branches of the media not forked. The first superior branch of the radius is nearly 2 mm. before the apical fork (or origin of last inferior branch) of media. The subcostal vein is thin, but quite distinct, and is joined to the radius by oblique cross-veins, some having a sigmoid curve. The costal field is finely reticulated, agree- ing herein with Stagmomantis and not with Photina. The width of the tegmen in middle is a little over 8 mm. Miocene shales of Florissant, Wilson Ranch (H. F. Wickham). REVERSION or ARCTIC HREBIA LIGEA var. ADYTE, Hs., anD ALPINE PARARGE MARA var. ADRASTA to THE TYPE-FORM. HIBERNATION or PYR4A- MEIS ATALANTA ann PARARGE EGERIA var. EGERIDES. By H. Rownanp-Brown, M.A., F.E.S. Mr. Wiuuiam Carter, of Hamburg, has been good enough to furnish me with a copy and translation of a paper communi- cated by Herr August Selzer to the Entomological Society of Hamburg, which contains several items of considerable interest to those of us who study the bionomics of the western pale- arctic butterflies. For some time in the arrangement of the genus Hrebia considerable doubt appears to have existed as to the actual species of which Hubner’s adyte is a variety. If any such doubt remains at the present, it should be finally dis- pelled by the results of the breeding experiments successfully carried through by Herr Seizer who, from ova obtained from Lapland adyte, has derived typical ligea. Adyte was common enough at Abisko, Swedish Lapland, when I was collecting there in July, 1906 (‘ Entomologist,’ xxxix. p. 247), and it was here, also, that Herr Selzer took the females from which he bred the typical form in Hamburg. REVERSION OF ARCTIC EREBIA LIGEA, ETC. 35 They were placed upon grass immediately, and commenced laying; the ova were kept, out of doors, and the larve emerged in the February of 1911, being half-grown at the end of June, when they proceeded to estivate. Reappearing at the end of August, they fed up and pupated, being now kept in a warm room. The first imago appeared on October 12th, the last on December 31st. The larve differed considerably in appearance from the ordinary form of Harz ligea, being darker and plainly striped. In nature ligea ova lie over the winter, and Herr Selzer says that “the larve which emerge in the spring hibernate the winter following,’ an imago rarely occurring late in_ the summer; so that the life-cycle of the typical ligea of the Harz extends apparently through two years. A comparison of adyte imagines from the Engadine and from Zermatt showed them to be identical with the Lapland form. Those in my own collection do not differ materially from examples from Cortina, the Brenner, &c., and, as I said before (loc. cit.) of the Abisko specimens, the superficial differences from the type are not marked in the male to any great degree. But those bred from Herr Selzer’s Abisko ova were absolutely identical with the EH. ligea from the Harz Mountains. Mr. Carter kindly sent me also a photograph illustrating in detail the results of this experiment, but, unfortunately, | am unable to reproduce it in this Journal, owing to the size of the block. It would be interesting to discover how far Lapland adyte, bred under natural conditions in Hamburg, would approximate to the type. But, as Herr Selzer claims, the contention as regards the specific identity of adyte and ligea may now be considered settled. As throwing further light on the subject of type reversion, Herr Selzer proceeds to record his experiences with Pararge mera var. adrasta. From females of this variety captured at Zermatt, sent to Hamburg for the purpose, ova were obtained, the larve still differing slightly from Harz typical form. But no difference was observable between the resulting imagines and the typical form. So that it may be inferred that the change back, due no doubt to altered conditions of climate and tempe- rature, comes about in the pupal phase principally, as has been demonstrated, I think, by the experiments of Mr. Merrifield and others. Two further notes by the same author, communicated to the ‘Internationalen Entomologischen Zeitschrift’ (No. 42, Jan. 18th, 1913, p. 298) on the subject of hibernation are also exceptionally interesting to British lepidopterists. Herr Selzer says that he found a freshly emerged Pyrameis atalanta at Heiligenhafen, on the Baltic, in the early part of June, and regarding this as an indication that the butterfly passes the winter in the pupal phase, he searched the same spot lies in ae 36 THE ENTOMOLOGIST. the year for larve, found them, and through the winter of last year had live pupe in his cages. ie ea tells us that of the larve of Pararge egeria var. egerides* (usually single-brooded in the Harz) obtained from captured females in June, half fed-up and emerged in Hamburg in the following September, the rest pupating at the end of that month and in October, and in this phase hibernating for a spring emergence. A NEW MOSQUITO FROM SAMOA. By Frep. V. Taropap, M.A., F.E.S., &c. Pseudoteniorhynchus samoensis, n. sp. Head brown, with narrow pale border around the eyes and pale line in the middle, a dark patch on each side ; black upright scales all over the head. Proboscis almost black, with a median creamy band. Thorax deep brown, with somewhat marked median lines and two pale spots before the bare space in front of scutellum. Abdo- men deep blackish-brown, unbanded except for a narrow pale basal broken band on the last segment, with basal, almost white, lateral spots; venter with third and fourth segments with basal pale bands, the fifth with a line of pale scales at the apex, others with traces of basal bands. Legs deep brown, narrowly banded, the bands mainly basal, but traces on the apices. Wings brown scaled. ?. Head shiny blackish, with a few small pale narrow-curved scales and numerous upright black forked scales all over it, a line of pale narrow-curved scales around the eyes and small flat grey and dark lateral scales, a median nude line appearing pale; proboscis rather thick, black with a median pale creamy band, black chet ventrally at the base; palpi moderately long, black-scaled; clypeus deep brownish black. Thorax black, with small, narrow-curved thin brown scales, very dense, two spots of similar but pale golden scales before the bare space in front of the scutellum, traces of two median parallel bare lines showing as dark lines, with two lines of paler hairs in the middle and others at the sides; lateral chetz black, very dense over the wing-roots and a number on each side of the bare space passing back to the scutellum; scutellum paler, with small narrow-curved dark scales and long black posterior border-bristles, dense on the lateral lobes: metanotum brown; pleure black and grey with some small flat whitish scales. Abdomen black, unbanded, with small basal creamy white lateral spots, which are prominent on the last segment, nearly forming a band; posterior border hairs pallid; venter with basal pale bands, the fifth with a white band near or on the apical border; on the sixth and seventh segments the basal lateral spots spread out along the sides of the segments to some extent. Legs dark brownish black, the fore pair with a small apical yellow spot on femora and tibiz and on the first four tarsals basal pale A NEW MOSQUITO FROM SAMOA. 37 bands; in the mid pair very similar, but slightly more prominent ; in the hind the banding still more prominent, in all traces of it on the apices of the segments; femora and tibie with numerous black chet ; ungues small, equal and simple. Wings rather narrow, with dense brown scales, rather broad and straight with shorter and broader median vein-scales; first fork-cell longer but about the same width as the second fork-cell, their bases about level; stem of the first not quite half as long as the cell; stem of the second about half as long as the cell; posterior cross- vein much longer than the mid cross-vein close to it. Halteres with pale stem and large fuscous knob with pale scales, especially at the apex. Length, 4°8 mm. Habitat.—Apia, Samoa. Observations.—Described from a single perfect female sent me by Dr. K. Friederiks, Government Zoologist of Samoa; two specimens were taken in a privy. It forms a very marked species of Pseudoteniorhynchus, easily told by the brown thorax having no posterior pale spots and by the abdominal ornamentation. The type I have presented to the Liverpool School of Tropical Medicine. Dr. Friederiks tells me the other mosquitoes found in Samoa are Stegomyia fasciata, Fab.; Stegomyia pseudoscutellaris, Thorp ; Culex fatigans, Wied; and a species of Mansonia (i.e., Temorhynchus). SYNONYMY OF ICHNEUMON OBLITERATUS AND I. BARBIFRONS. By Cuaupe Mortey, F.E.S8. Some time ago Dr. T. A. Chapman was so good as to present me with a female of Ichneumon obliteratus, Wesmael (Ichn. Miscellanea, 1855, p. 18), which emerged on August 21st, 1910, from the pupa of Brenthis pales, found at Furka, in Switzerland, on 28th of the previous month. When first describing the species, Wesmael knew but a single female: ‘‘ M. le Dr. Kriech- baumer a pris cette femelle aux environs de UVoire, en Suisse.” Giraud (Ann. Soc. France, 1877, p. 898) says Fallou bred it— evidently still the female only—and adds in a footnote, ‘“‘ L’ J. obliteratus provient de chenilles d’Argynnis pales prises en juillet 1866, autour de l’hospice du Simplon, dans le Valais,’ Switzer- land. Berthoumieu in 1894 simply epitomises this (somewhat incorrectly), and adds “‘ Holstein,” in Prussia, apparently on his own authority. ‘‘ Male inconnu.”’ Dr. Chapman has just sent me three more females with a single male, bred during August, 1912, at Col d’Iseran, in the 38 THE ENTOMOLOGIST. Graian Alps of Savoie, France, about fifteen miles north of Mt. Cenis, at 9000 ft., from pupx of Gnophus celibaria. The females are cospecific with the above, and the male is quite certainly its alternate sex, which has not hitherto been associated with it, though described by Holmgren in 1878 (Verh. z.-b. Ges. Wien, xxvii. p. 173, in his ‘‘Hnumeratio Ichneumonidum exhibens species in alpibus Tirolie captas’’) in the male sex only under the name Ichnewmon barbifrons, on account of the elongate capital pilosity found only in this sex, or to a much less degree in the female. His description is excellent, but he indicates no more exact locality, and no one has since recognized the species. Monk Soham, Suffolk: October 15th, 1913. NOTES AND OBSERVATIONS. Unusuat Patrinc or Morus.—I was interested to see in the ‘Entomologist’ for November, 1913 (vol. xlvi. p. 314), Mr. A. E. Hodge’s note upon the pairing of a male N. xanthographa with a female C. graminis. Some years ago, whilst living in London, I had a male H. versicolor pair with a female Prodromaria. Many ova were laid, but these proved infertile and soon shrivelled up.— G. Bertram KersHaw; West Wickham, Kent, November 3rd, 1913. Note Inuustratinc Minpness oF tHE Past Season. —I cap- tured a very worn male of Percnoptilota fluviata on my study window on September 30th, a perfectly fresh male on October 25th, and a third male in good condition on November 26th. This seems to indicate the maturing of two broods after the end of September. Vanessa urtice appeared in the garden on November 24th. A bat was hawking round street lamps on November 23th.—H. N. C. Stowe; Laleham, Bexhill-on-Sea, December 12th, 1913. NOTE ON REARING DasypouIA TEmpLI.—In July of last year I collected a number of larve of D. templi in the neighbourhood of Kinloch Rannoch, but from over thirty larve I only bred two insects, all the rest being stung. This year, in July, I collected more larvee in Cornwall, and practically all these attained the imago stage. The Scotch insects emerged on September 20th and 26th, while the Cornish insects did not begin to appear until October 28th, and continued till November 12th. This may have been caused by the difference in the two seasons, but I think it more probable the Scotch winter being earlier, insects from there habitually emerge at an earlier date. The larve are easy to find in infected plants of Heracleum sphondylium, and very easy to rear, in my experience. All that I did was to dig up with a trowel infected plants and replant them in a large tin or rhubarb pot, together with a few uninfected plants—and this I covered with a perforated zine cylinder with a muslin top. The larve required no attention, and when full NOTES AND OBSERVATIONS. 39 fed left the plants and pupated in the surrounding earth, without any cocoon.—Prrcy C. Rem; Feering Bury, Kelvedon. DraGonrules Brep in 1913.—I have bred this year Gomphus vulgatissinmus (one), 4’schna grandis, Cordulia enea, Libellula quadri- maculata, Sympetrum striolatum, Pyrrhosoma nymphula, Ischnura elegans, Hrythromma naias, and Calopteryx virgo. The nymph of Gomphus vulgatissimus was obtained in the New Forest in May. It is the first time I have taken one of this species, though I have for some years collected nymphs (and bred, too) in the same place in the forest, on one day at any rate, in early summer. I got no Cordulegaster annulatus this year, though they have generally turned up there, or, more accurately, have been turned up. A few hours on the Ouse, near St. Ives, in early June produced many Ischnura elegans and one nymph—an Anisopterid—which I have not yet been able to identify. It is growing fast, living mainly on small snails; but it is now taking to worms, which it refused for a long time.— Haroup Hopes; 9, Highbury Place, London, N. PLEBEIUS (LCaiNA) MEDON (ASTRARCHE) IN DoveDALE.—Referring to the note of Mr. St. John (vol. xlvi. p. 314), I was in Dovedale in July, 1908, and found this species quite common and I secured, as did Mr. St. John, quite a good series of thoroughly typical specimens. Insects generally were decidedly scarce, though I took one specially prettily marked blue female of Polyommatus icarus. Nudaria mundana was not uncommon on the walls of the outbuild- ings of some of the farmyards, whilst Boarmia bistortata lariciaria, Dbld. occurred in the dale. I also took one or two pretty Cerostoma sequella—and, apart from lepidoptera, Sirex gigas females were seen several times, though I only took a single specimen.—G. T. BeTHunz- BakER. : A Draconriy at SeA.—On September 6th, somewhere in mid- sea, between Kevel and Helsingfors, I saw the insect flying about over the deck. It subsequently settled on a chair, where it was caught by a fellow-passenger, who gave it to me. The presence of this dragonfly seemed curious, since there was no land within a good many miles, neither had we touched land since leaving England. —Joun B. Hicks; Stoneleigh, Elmfield Road, Bromley, Kent, November 8th, 1913. Wasps Active Iv DEcEMBER.—On December 5th I was much interested watching wasps, apparently workers, going in and out of a nest in the ground. This must be unusual.—H. C. StowzLt; Laleham, Bexhill-on-Sea, December 12th, 1913. PoLIA FLAVICINCTA IN GLAMORGANSHIRE.—I took this moth at sugar on October 2nd last in my garden. I can find no record of its being taken in this county before.—E. U. Davin; Yscallog, Llandaff, November 24th, 1913. NoLa ALBULA IN Hants.—I have much pleasure in reporting the capture of Nola albula whilst’ collecting in Hampshire (about July 18th and 19th). My friend, Mr. Danby, has two specimens, and I 40 THE ENTOMOLOGIST. have one. Others were taken, but unfortunately got damaged in travelling. Am I right in believing this to be a new record for the county ?—ArtHurR Buss; 43, Gleneldon Road, Streatham, 8. W. ACRONYCTA MENYANTHIDIS EMERGING In NovEMBER.—On looking in my pupa-cage on November 3rd, I was surprised to find that a female specimen of Acronycta menyanthidis had emerged from pupe sent me from “ Barnard Castle,” all collected this year. They were kept in a glass-top bottle in a room with no fire, temperature about 55° to 60°. I thought it would be interesting to record this, because I can find no record of so late an emergence.—H. L. Douron; 27, Brunswick Street, Reading, November 17th, 1913. HARIAS CHLORANA IN GLOUCESTERSHIRE.—In August, 1912, the Rev. G. M. Smith found about a dozen larve of this species feeding on the osiers growing on the Severn bank near Gloucester. One or two imagos emerged in the following September, but the rest hibernated as pupee and came out at intervals during May, June, and July of this present year. It is curious that this species has not apparently been observed in this county hitherto.—C. GRANVILLE CLUTTERBUCK, F.E.S.; 23, Heathville Road, Gloucester, November 16th, 1913. Hypotion (CHHROCAMPA) CELERIO IN Hants.—A specimen of C. celerio was caught by a cat in a house in this parish last September. The locality is less than a mile from the sea, between Lymington and Christchurch. -—(Rey.) J. E. Kentsatn; Milton Rectory, New Milton, November 22nd, 1913. DapPHNis (CHAROCAMPA) NERII.—One of these very rare visitors occurred here this season, and was captured on September 16th. The moth was seen on the wing at about 4.15 p.m. by two small village boys, who eventually succeeded in their endeavours, with the aid of their caps, &c. The following day it was brought to my house (partly for identification), being a pitiable sight but still alive; it is, nevertheless, sufficient to serve as a record. My friend Mr. Brown of Ainsdale kindly lent me the moth for exhibition at the November meeting of the Lancashire and Cheshire Entomological Society.— W. A. Tyerman; Derby Villa, Ainsdale, Southport, November 19th, 1913. CATOCALA FRAXINI IN Lancos.—A specimen of Catocala fraxint (Clifton Nonpareil) was caught at Grange-over-Sands, Lanes, September 7th, 1913, in the grounds of Yewbarrow Hall, the residence of Hvan A. Leigh, Esq.—J. Davis Warp; Limehurst, Grange-over-Sands. Conias EDUSA REARED IN Kent.—On May 23rd, 1913, my son brought to me a female Colzas edusa he had caught with his cap in a waste field not fifty yards away from our house. I succeeded in keeping it alive for three weeks. During that time it kindly obliged with one hundred and fifty ova; these I placed singly in airtight tins with a glass top, my intention being to try for a second brood, but the larvee grew so slowly that I had to abandon the idea. The first imago emerged on August 15th and the last on September 9th. I NOTES AND OBSERVATIONS. 41 might add the larva were kept indoors and out of the sun, so probably this had something to do with slow growth. Altogether I bred a nice long series, but with little or no variation —A. J. HxETER; Watling Street, Dartford, Kent, October 17th, 1913. Cormias EDUSA IN MippLEsEx.—Jn previous Hdusa years I have usually observed one or two examples here in August or September. But this season the ‘‘clouded yellow” has not put in an appearance. However, my cousin, Dr. R. P. Cox, of Ealing, informs me that in August several visited his garden; and he reports it also to have been not uncommon at Shipley, in Sussex, and at Torquay.—H. RowutanD-Brown ; Harrow Weald, December 15th, 1913. Novss on Conias EvusA, &c., IN Essex.—I first noticed C. edusa here on August 20th. The next day I visited a small field of lucerne about ten minutes’ walk from my house. On the way a bright looking female edusa passed me in the road, but my net was in my pocket. On reaching the field not a specimen of edusa was to be seen, but after waiting for nearly an hour, a male flew by and settled on one of the lucerne flowers and was captured, and in the course of half an hour I saw three more, and caught two of them—both males. There was a fair amount of bloom on the lucerne, and it was a warm bright afternoon, but butterflies were very scarce. I only noticed single examples of Pyrameis atalanta, P. cardut, Vanessa 20, a few fresh V. urtice, and one or two each of Cenonympha pamphilus, Lycena acarus, Chrysophanus phig@as, and Adopea lineola. Pararge megera was the most numerous, and there were a few Pers rape and P. napi which were noticeable on account of their small size. Two of the napi I caught are, I think, the smallest I ever saw, measur- ing barely 14 in. across the wings. A few Plusia gamma were buzzing about amongst the flowers, and one or two Nomophila noctuella (S. hybridalis) were disturbed from the herbage. On August 25th I saw a large female edusa flying along the high road. The next day I went to Walton-on-the-Naze, as I thought that might be a more likely neighbourhood, and I particularly wanted to get a female C. edusa for eggs. On arriving at Walton I walked out to the eastward of the town, by the footpath on the top of the cliffs, and when about half way to the Naze saw a bright-looking female flying about willow herb some distance below me, but she would not come within reach, nor could I get down to her. Further on I was pleased to see, on my left, a large clover field one mass of bloom—indeed, I smelt it long before I saw it. Here I thought I should surely find all the edusa in the neighbourhood congregated, but was disappointed, for when I got into the field, nothing was to be seen but a few rape, napi, &e. I stopped there for more than an hour, sat under a hedge, eat my lunch, and smoked a pipe, but no edusa would come. It was gloriously hot and bright—just the day for them. After this I walked a little further along the coast, beyond the Naze, and then turned back, as it was time to go to the station for my train home— and I had hardly done so when a male edusa came dashing along and was secured. On the 28th I saw another male at Dovercourt, and this was the last. 42, THE ENTOMOLOGIST. On August 27th I received five living females from my friend Commander Gwatkin- Williams, R.N., who had taken them the day before at. Broadstairs, where C. edusa appears to have been rather plentiful. They were placed under muslin hoods over growing plants of white clover and birdsfoot trefoil in flower-pots, and put in a warm place in the garden. Next day I saw a good many eggs had been laid, and by the time the last female died, two or three hundred ova had been deposited. The eggs were pearly-white at first, but soon changed to orange, and by September 2nd some had become lead colour, and larvee began to hatch out the following day. The young larvee were dingy-olive, with shining black heads, and their first act was to devour their egg-shells, then, after they had rested a bit, they wandered about, and finally settled either in the middle or at one of the corners of a leaf, and began to nibble at the upper cuticle, making small blotches. They laid up for their first change on September 10th, and some had got through by the 12th, and were then dull green, with minute black dots and short pale hairs. I will not give any further account of their progress, as that has been done so many times by other writers. The pots were kept in a window facing south, and everything went well with the larve until the temperature began to fall towards the beginning of October, when many of the smaller ones began to sicken and die off. Some of the larger ones by this time were nearly full grown. On October 9th I noticed one had attached itself to the side of the muslin hood, and the next day became a pupa. By the 17th there were a dozen pupe, but scores of larvee had died, and those remaining would not eat, and eventually they all perished. None of them appeared to make any attempt to hibernate. By this time it was getting very much colder, and I had started a fire in my sitting-room. All the pupx were now pinned to a sheet of cork, and this was placed under a glass cylinder, with a French Clocke over it, on a table close to the window, where they got the full benefit of the sun. On the 26th the first pupa began to change colour, and by the 31st the wing cases were bright orange, and the black margins of the wings plainly visible, and on November 2nd, about noon, I observed the butterfly trying to escape from its chrysalis, and it had evidently been trying for a little time before I noticed it, as its wings were hanging down partially developed, so I lifted glass and cylinder and, with a pair of forceps, managed to free it, but it was then so feeble it could not grasp anything, and I had to hold it by its front legs, after which I managed to tie a piece of silk round them, then passed the silk over a pin in a piece of cork and left it, and eventually the wings grew to their full size, though one of them was slightly puckered, but I managed to smooth this out when I set it. Other pups were changing colour at this time, but most of the butterflies seemed to be unable to emerge, and I only bred five altogether, viz: November 2nd, one male; November 6th, one female; November 9th, two males; November 11th, one male. Unfortunately I have no greenhouse, if I had I should no doubt have bred a larger number of the butterflies—GrrvAsE F. Matnew; Lee House, Dovercourt, November 17th, 1913. 43 SOCIETIES. ENNTOMOLOGICAL Society oF Lonpon.— Wednesday, November 5th, 1913.—Mr. G. T. Bethune-Baker, F.L.S., F.Z.S., President, in the chair.—Mr. A. P. Semenoff Tian-Shanski was elected an Honorary Fellow in the place of the late Prof. O. M. Reuter.—The following gentlemen were elected Fellows of the Society :—Messrs. Hugh Warren Bedford, Church Felles, Horley; Harold $8. Cheavin, F.R.M.S., F.N.P.S., Clematis House, Somerset Road, Huddersfield; Charles Alban William Duffield, Stowting Rectory, Hythe, and Wye College, Kent; W. Egmont Kirby, M.D., Hilden, 46, Sutton Court Road, Chiswick, W.; Louis Meaden, Melbourne, Dyke Road, Preston, Brighton; F. V. Bruce Miller, Livingston, N. Rhodesia; Alexander David Peacock, 137, Wingrove Gardens, and Armstrong College, New- castle-on-Tyne; H. Ananthaswamy Rao, Curator of the Government Museum, Bangalore, India; Percival Nathan Whitley, New College, Oxford, and Brankwood, Halifax.—The question of the change of title of the Society was opened for discussion, but the preponderance of feeling appeared to be somewhat against any change.—The President brought before the meeting the necessity of forming a fund for the care of that portion of Wicken Fen left by the late Mr. G. H. Verrall to the National Trust, and at his request Mr. Rowland-Brown expressed his readiness to act as Treasurer for any subscriptions given by Fellows of the Society.—Dr. G. B. Longstaff exhibited a series of seventeen Thais rumina, L. (including a female of the var. cantener, Held.), taken in March, 1918, at Ronda, and called atten- tion to the characters suggestive of a distasteful butterfly —Mr. W. J. Lucas, three species of Panorpa, including a female of the scarce scorpion-fly, Panorpa cognata.—Mr. H. Lupton, a specimen of U'halpo- chares ostrina, taken in the middie of June, 1913, about four miles from Ilfracombe. Also two specimens of Dianthacia luteago vay. ficklina, taken in the middle of the same month on the coast of N. Devon.— Dr. G. D. H. Carpenter read notes in connection with his exhibit of Epitoxa albicincta. He also exhibited a case of miscellaneous insects and communicated notes upon them. — Mr. Donisthorpe exhibited males, winged females, and a deilated female and workers of the very rare ant, Solenopsis fugax, Latr., taken at Blackgang, Isle of Wight, on August 26th, 1913—Mr. HE. E. Green, an aberrant example of Pyrameis (Vanessa) indica, Herbst, from Ceylon.—Comm. J. J. Walker, a female specimen of the gigantic Neuropteron, Corydalis orientalis, Mclach., taken by a native collector at Chuchow.—Mr. L. W. Newman, the following Heterocera :—(1) Calymnia (Cosmia) trapezina. A melanic female—a worn specimen taken at sugar in Bexley Woods. (2) Zonosoma (Ephyra) annulata and pendularia ; a long and very varied series of both species, showing extreme light, dark, and intermediate forms and one very pink Z. pendularia. (3) A series of hybrid Z. pendularia, female, and annulata, male ; specimens showing the markings of pendularia most pronounced and the coloration of annulata prominent.—The following papers were read :—‘‘ New or little-known Heterocera from Madagascar,” by Sir G. H. Kenrick, Bart., F.E.S. ‘The Culicide of Australia,” by Frank H. Taylor, F.H.S. ‘Descriptions of New Species of Staphylinidee 44 THE ENTOMOLOGIST. from India,” by Malcolm Cameron, M.B., R.N., F.H.S. “ Pseudacrea eurytus hobleyz, Neave, and its models on Bugalla Island, Lake Victoria, with other members of the same combination,” by G. D. H. Carpenter, B.A., M.D., F.E.S. “ Pseudacrea boisduvalt, Doubl., and its models with special reference to Bugalla Island,” by the same. “The inheritance of small variations in the pattern of Papilio dar- danus, Brown,” by the same. Wednesday, November 19th, 1913.—Mr. G. T. Bethune-Baker, H.L.S., F.Z.S., President, in the chair.—It was announced that the Council had decided to make an annual grant of two guineas towards the maintenance of Wicken Fen.—The following gentlemen were elected Fellows of the Society :—Messrs. B. G. Adams, 15, Fernshaw Road, Chelsea; Barnard Ormiston Dickinson, B.A., 57, Castelnau, Barnes, 5.W.; Alfred Oliver Rowden, 3, Archibald Road, Exeter ; Oscar Whittaker, Ormidale, Ashlands, Ashton-upon- Mersey, Cheshire. —The following Fellows were nominated by the Council as Officers and Council for next year:—President, Mr. G. T. Bethune-Baker, H.L.S., F.Z.S.; Treasurer, Mr. A. H. Jones; Secretaries, Commander J.J. Walker, M.A., R.N., F.L.8., and Rev. G. Wheeler, M.A., F.Z.S.; Librarian, Mr. G. C. Champion, A.L.8., F.Z.8.; other Members of the Council: Messrs. E. A. Butler, B.A., B.Sc.; J. E. Collin; S. Edwards; Dr. H. Eltringham, M.A., D.Sc., F.L.S.; C. J. Gahan, M.A.; A. E. Gibbs, F.L.S., F.Z.S.; E. HE. Green; G. Meade-Waldo, M.A.; Dr. G. W. Nicholson, M.A., M.D.; Hon. N. C. Rothschild, M.A., F.L.8., F.Z.8.; H. Rowland-Brown, M.A.; and C. J. Wain- wright. — Mr. A. H. Jones exhibited specimens of both sexes of Pleberus zephyrus var. hesperica, taken by him in June last, at Albarracin in Spain; P. zephyrus, type, and var. lycidas were also exhibited for comparison. Also from Albarracin, Melite@a desfon- taint var. betica, Rbr., the Spanish form of M. desfontainii, Godt., (an Algerian butterfly); both sexes were exhibited —Mr. E. E. Green, two Pierid butterflies, of distinct genera, taken am cotta at Aripu, Ceylon, viz., Appias lbythea, Fab., male, and Teracolus limbatus, Butl., female. — Mr. W. J. Kaye, a large and very variable series of Heliconius doris, L.—Dr. Chapman, some Erebias, showing parallel variation in several species in different localities. He raised the question whether this was a case of mimicry, and a considerable discussion followed.—Dr. F. A. Dixey, a drawer containing specimens of the genus Pzerzs, with drawings of their scent-scales, and remarked upon them.—Mr. A. Bacot, slides showing the development of Plague bacilli in the alimentary canal of the flea, and the method of infection through the mouth, and read an important paper on the subject.— Dr. K. Jordan, some specimens of a lepidopterous larva discovered by the Rev. A. Miles Moss, F.E.S., who, when collecting near Para, noticed a Saturniid caterpillar with black intersegmental bands and long branched spines, a species of Auwtomeris, some of the black bands of which appeared to be swollen. To his amazement these swellings, when touched, quickly slid over the back of the caterpiltar to the other side with the hurried motion of a Pyralid larva, and indeed turned out to be small lepidopterous larvee as black and glossy as the bands of the Automeris caterpillar.—The following papers were read :—* Revision of the Mexican and Central American Malachiide SOCIETIES. 45 and Melyridw, with descriptions of new genera and species,” by George Charles Champion, ¥.Z.S. ‘ Four new genera and species of Hymenoptera from Australia,” and ‘‘ Three new species of Australian Hymenoptera,” by A. A. Girault, communicated by A. M. Lea, F.E.S., Government Entomologist, South Australia—Guro. WHEELER, M.A., Hon. Secretary. THe Sovuta Lonpon EntomonocicaL anpD Naturau History Soctety.— October 9th, 1913.--Mr. A. E. Tonge, F.H.S., President, in the chair.—Large additions to the Society’s reference collection of British Lepidoptera from Mr. W. G. Dawson were announced.—Mr. Lucas read a paper: ‘The Shorthorned Acridians of the British Isles,’’ and illustrated his remarks with lantern slides of all the species—Mr. Ashdown exhibited Lepidoptera taken by him in Switzerland in June and July last.—Mr. Colthrup, a snail shell from which he had bred a Dipteron, presumably parasitic in the snail.— Mr. Andrews, a scarce Dipteron, the Syrphid S. guttatus, taken at Bexley in August.—Mr. Step, living examples of the ant-nest Isopod Platyarthrus hoffmannseggii, found in a nest of Formica fusca.—Mr. West (Ashtead), enlarged photographs of the same rare woodlouse. —Mr. Curwen, specimens of Syntomis phegea ‘and its var. pflwemeri, in which the white spots were reduced in size and number, from Pallanza and Iselle, together with specimens of the rare Nacha ancilla.—Mr. Newman, picked series from a large number of bred Melitea aurinia, from County Clare and Oban. The variation was extremely small, although the larvae were samples of many broods.— Mr. Tonge, a series of Coremia quadrifasciaria, bred from a female taken at Albury, Surrey, showing but little variation. October 23rd, 1913.—Mr. A. E. Tonge, F.E.S., President, in the chair.—Prof. E. B. Poulton, F.R.S., gave an account of the Mimicry exhibited by the Nymphalines of North America, illustrating his remarks by specimens and lantern slides.—Mr. W. J. Kaye exhibited a collection of the Sphingidee found in the Island of Trinidad. There were about forty species in all.—Mr. Sheldon, series of species taken by him near Albarracin, Central Spain, including Pleberus zephyrus var. hesperica, Agriades thetis ab. rufolunulata, A. thersites, and Glaucopsyche cyllarus. Dr. Chapman was of opinion that A. thersztes only occurred when sainfoin was indigenous.—Mr. L. W. Newman, Lepidoptera from County Clare, County Cork, and Killarney, in- cluding very light Aplecta nebulosa, very dark Luperina cespitis, Aphantopus hyperanthus, with greenish shade on the under side, Aiigeria scoheformis, bred Dianthaecia capsophila, D. luteago var. barrettw, &e. The weather was very bad from April to the end of September.—Mr. A. E. Tonge, a specimen of Argynnis aglava, with a strongly marked blotch formed by the coalescence of several spots on the fore wings. November 13th, 1913.—Mr. A. E. Tonge, F.E.S., President, in the chair.—Prof. W. Bateson, F.R.S., gave an address on the ‘Problem of Species which overlap Geographically,” illustrating his remarks with numerous lantern slides—Mr. Curwen exhibited specimens of Parnassius apollo from Eelépens and the Laquinthal, mostly very large examples, and including var. psewdonomion from Helépens.— 46 THE ENTOMOLOGIST. Mr. Newman, long and variable series of Zonosoma annulata and Z. pendularia, with many dark aberrations; and also a series of the ere between these two species, showing well the characters of oth. November 27th, 1913.—The President in the chair.—The Annual Exhibition of Varieties, &¢.—Mr. West (Greenwich), the Hon. Curator, fifteen cabinet drawers of the Society’s reference collection, with which had been incorporated a portion of the Dawson collec- tion.-—Dr. Chapman, a nearly black Argynnis aglaia from Le Lauteret, July 13th, 1913, and specimens of Agriades thersites, Polyommatus wcarus, and var. icarinus, with diagrams to show the different align- ment of spots.—Mr. Edwards, a box of conspicuously coloured Heterocera from Burmah.—Mr. H. Moore, the rare Papilio hecateus from the Solomon Islands.—Mr. Schmassmann, a series of varieties in the male of Ornithoptera hecuba, and a pair of the gorgeous O. alecandre from New Guinea.—The Rey. G. Wheeler, examples of melanic and xanthic aberrations, including Argynnis niobe ab. pelopia, Melitea phebe ab., M. varia ab., M. cinxia ab., and Melanargia ab. of the former, and A. niode v. erts, Callimorpha dominula v. persona, &e., of the latter, and referred to many species in which yellow was produced in aberrational forms.—Mr. R. Adkin, a series of third brood Celastrina argiolus, and discussed the species as to its appear- ance during the present season. He also showed long series of Agriades corydon, including ab. syngrapha, ab. semisyngrapha, and many other fine aberrations and series from many localities ——Mr. Baumann, a series of Boarmia repandata from several localities, including var. sodorenstwm and var. conversaria, and specimens of the melanic form of Acidalia virgularia, which he was placing in the Society’s collection.—Mr. Bright, a large number of striking aberra- tions of British Lepidoptera, including long series of under sides of Agriades thetis and A. corydon, a white aberration of Argynnis paphia, Colas edusa, with wings richly shot with purple, a curious Saturnia pavonia of female coloration with male antenne, &c.—Mr. Grosvenor, his fine collection of Cenonympha tiphon and its local races.—Mr. Curwen, numerous Lyczenide taken by him in Italy and Switzerland, and many aberrations of Melitea didyma.—Mr. Newman, a varied series of recently bred Smerinthus ocellatus ; series of Amorpha popula from pale cream to almost black colour, with intermediate and rich pink forms ; and a series of hybrid ocellatus males and popula females, two being of the rare female form.—Mr. A. Gibbs, a section of his collection of South American Nymphalids, including many of the brilliant species in the genus Perisamia.—Mr. W. G. Sheldon, long series of Melitea desfontainit, taken by him at Albarracin this year, and a series of M. awrinia v. therica, from near Barcelona, for com- parison.—Mr. T. W. Hall, cabinet drawers of Agriades corydon and A. thetis, showing great aberration with very pronounced blue females, and some females curiously splashed with blue.—Mr. Main, frames containing series of photographs of the life-histories of Cicindela campestris (tiger-beetle), Chrysopa flava (lace-wing fly), Phyllotoma aceris (jumping sawfly), &e.—Mr. Tonge, a bred series of Psilura monacha, including the black form ab. eremzta; a long series of T'apinostola concolor, &e.—Mr. W. J. Kaye, a case of twenty-three SOCIETIES. AT pairs of the South American genera Melinea and Heliconius, found flying together and assimilating to each other in colour.—Com- mander Gwatkin- Williams, aberrations of British Lepidoptera from Treland, including Epinephele jurtina, with banded hind wings, females; several Czdaria, which possibly may be C. concinnata, Xanthorhoé montanata, with band obsolete, confluent Anthrocera trifolit, Huchloé cardanunes, females with ochreous hind wings, &c.— Mr. Chas. Oldham, two collections of small chalk stones that he had collected within a small radius of the openings of two wasps’ nests, and which the wasps had been unable to carry to a greater distance. —Mr. A. W. Buckstone, for Mr. Archer, a bleached form of Angerona prunaria, male, from Oxshott; an almost black Lithosia helvola (deplana) from Wimbledcn; and an Acidalia which was supposed to be a very aberrant form of A. subsericeata.—Mr. H. Worsley- Wood, numerous forms of Mellinia ocellaris, including ab. lineago, ab. inter- media, with M. gilvago for comparison; yellow Brephos parthenias from Wimbledon, and lead-coloured males of Agriades thetis from Corfe.—Rev. J. Tarbat, black suffused forms of Brenthis ewphrosyne ab. nigro-sparsata of Abraxas grossulariata, and a Cidaria truncata with a broad-banded fore wing.—Mr. Haynes, a series of hybrid Selenia tetralunaria males and S. bilunaria females, with a large preponderance of gynandromorphous specimens; melanic and ochreous varieties of Hnnomos quercinaria, &c.—Mr. H. J. Turner, a series of Hrebia stygne from the Continent to show the extreme local variation in the Alps and Pyrenees.—Messrs. Sharp & C. W. Colthrup, many Colias edusa from the south-eastern district, re- presentative of the species in 1913.—H. J. Turner, Hon. Rep. Sec. LANCASHIRE AND CHESHIRE ENToMOLOGICAL SocteTy.—October 20th, 1913.—Meeting held at the Royal Institution, Colquit Street, Liverpool.—The President, Mr. F. N. Pierce, F.E.S., in the chair.— Exhibitions were as follows:—Mr. W. Mansbridge brought a long- bred series of Hadena glauca from Burnley, some of which showed a strong melanic tendency; also from Burnley the melanic variation of Hmaturga atomaria, Hyria muricata, purple form, and Canonympha typhon var. rothliebiz from Witherslack; Nyssia zonaria from the Crosby Sandhills, and the insects captured on the occasion of the Society’s field meeting at Mold on June 7th, 1913, including Lobo- phora viretata, Cnephasia musculana, Capua favillaceana, Argyrolepia hartmanmana, and Agriopis aprilina (larva).—Mr. R. Tait showed a long and variable series of the beautiful melanic form of Boarmia repandata from Penmaenmawr, also bred Agrotis lucernea from the same district; varieties of Abraxas grossulariata, including ab. varleyata, bred from various localities in 1913; Aplecta nebulosa var. robsoni and Geometra papilionaria from Delamere; Hecatera serena and Calligenia miniata from Sussex. Mr. Tait also gave an account of his collecting holiday in Sussex, from which it appeared that Lepidoptera had been as difficult to obtain in the South of England as in the North during the past summer.—Mr. Johnson exhibited a long and fine series of C. typhon, including some very dark forms, from Witherslack; also Acizdalia fwmata, Nissoniades tages, and Lycena astrarche from the same place.—Dr. P. F. Tinne, various 48 THE ENTOMOLOGIST. species of autumn lepidoptera from the North of Ireland, including a nicely varied series of Cidaria truncata, several being the var. cen- tumnotata. All the members present reported a very poor season from a collector’s point of view.—Wmn. Manssripce, Hon. Sec. RECENT LITERATURE. Common British Moths. By A. M. Stewart. London: Adam & Charles Black. 1913. Pp. viii, 1-88. Sixteen plates. Tuts little book is a worthy companion-volume to the ‘ British Butterflies’ by the same author, already noticed in the ‘ Entomolo- gist’ for 1912, p. 212. The eight coloured plates are really of most excellent workmanship, one is inclined to think some of the best ever produced, certainly in entomological literature. They are splendidly clear, and marvellously accurate in colour. They contain figures of some two hundred species, all those mentioned in the text in fact, and though only three-fourths natural size it should be quite im- possible to identify wrongly any of the species figured. The black- and-white plates of preserved larve, &c., have been well chosen, the text is obviously the work of a practical entomologist, and the species described form a very excellent representative collection of the commoner British moths, amongst them, one is pleased to note, some of the ‘ Micros” being given a place. Errors of any kind seem exceedingly few, although it is difficult to understand how the specimen of Boarnua repandata var. conversaria, figured on Plate 15, came to be labelled “ B. gemmarza var. perfumaria,” probably by acci- dent. The book is absolutely ideal for the young beginner. N.. DR: Transactions of the City of London Entomological and Natural History Society for the year 1911. Pp. 32. Published by the Society, The London Institution, Finsbury Circus, 1912. WE have received a copy of the above Society’s ‘ Transactions ’ for 1911. Apart from the notes in the President’s address upon the season’s collecting and upon the scarcity of some insects formerly so common in their haunts, there is a short but quite interesting paper by Mr. Tautz upon the species of the genus Cosmia (Calymmnia). This includes a record of C. pyralina from Middlesex (Pinner), a species which the author states had not been previously recorded, so far as he knew, from that county, but here he is in error, as the species is pretty generally known to inhabit Middlesex, and was recorded from Mill Hill over thirty years ago. N..D) B. Zz “DATA” “LABELS FOR LEPIDOPTERA. 26 eee cn ‘1 to 6 sorts, equal numbers, any wording, see specimens below -— he a H. Smi ae Z VER, Davis, {a it Langley, ; ++ -F. Roberts, + Darenth Wed. wae "New Forest. Cty S Kents Rannoch. oy P 19° \ 19 If ‘anequal ate are ordered, 6d. extra will be charged. Minimum charge for small quantities, 16. These are’ neatly printed similar to the above. We have supplied these labels to Entomologists in all _ parts of Great Britain and abroad. We also supply labels for minute. insects printed in the Smallest Type made. (see specimens below). These are 3/6 per Ashish ow Davis, A us gle y mm F. Roberts, Daren \ Ws foo AL New ore Rannoch. 4 a W. DAVIS, “CONTAAOTONS, Museum Works, Dartford, CALIFORNIA. LEPIDOPTERA. UR Propagator and Collector of California Lepido- ptera again going to breed and collect in every locality of - California. Gentlemen and Museums wishing large quantities of yall taken, RY from 10 to 100 of each species, can ‘have them at a - flat rate of 23d. each. Parties wanting only certain species should send for my price list, and save 50 per cent. on retail prices. Still a few of this season’s catch on hand, Lycsena anna, 2s. per pair; this Lycena retails at about 8s. pair. Parnassius clodius, 2s. pair. Argynnis egleis, 1s. 3d. pair, &¢. Noctuide and Geometride, always _ 24d. each for quantity orders of from 5 to 100 of each species. ‘I'here are about 350 different species of Noctuidw.and about 200 different species of Geometride in California. Sent on approval, by my new system of mailing which insures us both. : Prof, Jas. Sinclair, 333, Kearney St., San Francisco, California. LEONARD TATCHELL & Co., Breeders and Collectors of British Butterflies and Moths. 23, THE ARCADE, BOURNEMOUTH. Offer their New Lists of LIVING LARVA and PUPA, Imagines, | _Life-histories, and APPARATUS. MANY GOOD VARS. & MELANIC FORMS. 10, 12; 15, 20, AND 40-DRAWER CABINETS FOR SALE, FULL PARTICULARS ON APPLICATION. : [LOCALITY LABELS FOR ENTOMOLOGISTS.— The * Data” label is now considered to be a necessary accompaniment of every. entomological Specimen; and a neatly PRINTED label is superior in every way to oné handwritten—being more compact, _ always legible, and effecting a great saving of time and labour. One to five localities, equal quantities; locality, date (191 ), and collector's name (three lines in all)—1000 for 2s. 6d., 2000 for 4s., 3060 for 5s.; locality and date only (two lines)—1000 for 2s., 2000 for 3s. 3d., 3000 for 4s. Unequal num- bers, or each additional line, 6d. extra. Special: MINUTE LABELS, printed in the smaLLest TyPE ap™, essential _ for Mieros., and the lesser Macros., or small insects of other orders ; specie and prices on application. FISTS, for pointing out yastetios, 6d. per 100, 300 for 1s. CAREFUL WORK GUARANTEED, CASH WITH ORDER, F. LITTLEWOOD, 22; HIGHGATE, KENDAL. qe ei tha we vee 33 ae hie : Some "Renusee on the Avandia ms of Sympetrum striolatum (with illustrations), Kenneth 74 orton, 1. Notes ‘on the Life-h Hesperia tessellum and H. crib rellum, Butterfly Hunt in some parts of Unex cae Feinnes H. Rowland-Br ) - Some Notes on the Lepidoptera of ‘La Sainte Baume, Var, S. France, (R _ By BE. Lowe, 14. Note on the ‘Oviposition of Rhyssa (with | illustrations ‘L.N. G. Ramsay, 20, A Mon yraph of the Genus Osprhynchotus, Spinol ~ Claude Morley, 23. Two New Myrmecophilous Aphides trom Algeria, (with illustrations), Fred. V. Theobald, 28. The Fossil Orthoptera of Florissant, Colorado (with illustration), we D, A. Cockerell, 32. Reversion of Aretic Erebia: ligea’ var: adyte, eeEDi, and Alpine Pararge mera var. adrasta to the Type: forni. Hybernation of Pyrameis atalanta and Pararge | egeria var. egerides, H, Rowland-Brown, 34. A New Mosquito from Samoa, Fred. V. Theobald, 36. Synonymy - of Ichneumon obliteratus and J. barbifrons, Claude Morley, 37. ii Norrs AND OBSERVATIONS. Regt aicial Bantes of Moths, G. Bertram 7» Mepahas 38. wa Note Illustrating Mildness of the Past. Season, H. N. C. Stowell, 38. Note’ - of Rearing Das a templi, Percy G. Reid,.38. Dragonflies Bred in 1918, Harold Hodge, 3 Plebeius (Lycena) medon (astrar che) i in Dovedale, G. T. 4 y _ ‘Bethwne-Baker, 39.. A Dragonfly at Sea, John B. Hicks, 39. Wasps Active ra ‘in Deeember, H.C. ‘Stowell, 89. Polia flavicineta in Glamorganshire, Bi Te David, 39, Nola albula in Hants, Arthur Buss, 39, Acronycta menyanthidis _ cna ae in November, H..L. Dolton, 40. Barias chlorana in Gloucester- F shire, C Granville Clutter buck, 40, Hipotion (Cherocampa) celerio in Hants, (Rev.) y) E.. Kelsall, 40. Daphnis (Chzerocampa) nerii, W. A. Tyerman, 40. Catocala fraxini in Lambs:, J. Davis Ward, 40. Colias edusa Reared‘i in Kent, A. J, Haxeter, 40. Colias edusa in Middlesex, H. Rowland- Brown, 41, Thuis é ‘on Colias aft sh, &e., in Essex, Gervase F. Mathew, 41. ‘ Romi, 43. “2 RECENT Literature, 48. a4 : “D® STAUDINGER & BANG- HAAS, Blasewitz- Dresden, in their: new Price List No. LYII. for 1914 (116 pag.), offer more than 20,000 — Species of well-named LEPIDOPTERA, set or in papers, from all parts. of the 1 “would, in finest condition; 1600 kinds of PREPARED LARVA, &c. SEPARATE. © Price Lists for COLEOPTERA. (80,000 species, 208 pag.), for HYMENO- | P'TERA (3600 species), DIPTERA (2900), HEMIPTERA (2500),ORTHOPTERA — (1200), NEUTERA (630), BIOLOGICAL OBJECTS (800). Discount ahs vee & orders. Priceslow. We sell no more living pupe. ; REMEMBER! ee The ORIGINAL and LARGEST BUTTERFLY FARM in the BRITISH ISLES is HEAD’S. (EsTaBLIsHED 1884.) AD Immense Stock of Fertile Ova, Living Larva & Pupe, & Set Specimens always on Sale, ~ - Many GOOD VARIETIES and HYBRIDS frequently in Stock. Apparatus and Cabinets of the best quality supplied. Price List sent fiat 4 Note the Address— ae Eto MV HEAD, Gntomnalaaee sey BURNISTON, NEAR SCARBOROUGH. JAMES GARDNER, MANUFACTURER of ALL KINDS of ENTOMOLOGICGAL APPARATUS P 52, HIGH HOLBORN, ann =. °. 29, OXFORD STREET, nearly opposite Tottenham Court Road PRICED LISTS ON APPLICATION. Steed ins pe All Articles Guaranteed : exchanged if not approved of. Friends and Customers ‘ are requested to note the REAP ERS as mistakes oceur daily.” ; tions. ie phe’ ‘Entomologist ' (6s. post je for 1914 are now due ould ne sent Ae Ad ig pawniar & Co., 54, Hatton Garden, London. tp ee ee FEBRUARY, 1914... (No. 609. re eran anaes eeaeMaN Naess ‘THE ENTOMOLOGIST | AN Plusteated Monthly Journal OF GENERAL ENTOMOLOGY. | “EDITED BY RICHARD SOUTH, F.-E.S. WITH THE ASSISTANCE OF | ROBERT ADKIN, F.E.S. C. J. GAHAN, M.A., F.E.S. H. ROWLAND-BROWN, M.A.,F.E.8. | W. J. LUCAS, B.A., F.E.S. W. L. DISTANT, F.E.S., &c. (CLAUDE MORLEY, F.E.S., F.Z.8, | F, W. FROHAWE, F.E.S., M.B.0.U.| Dr. D. SHARP, F.R.S., F.E.8., &c. { ‘*By mutual confidence and mutual aid : | - Great deeds are done and great discoveries made.” ~~ | 2 F hon Y¥ | : at sf ( : hen ae)! 4 e i Be 4 ) ey re } t Py m | LONDON: RAP . WEST, NEWMAN & CO., 54, HATTON GARDEN -SIMPKIN, MARSHALL, HAMILTON, KENT & CO., Limren. Price Sixpence. WATKINS & DONCASTER Naturalists and Manufacturer of Entomologico! Apparatus and Cabinets x i a Plain Ring Nets, wire or cane, including Stick, 1s. 8d., 28., 2s. 6d, Folding Nets, | 8a. 6d., 4s. Umbrella Nets (self- acting}, fs. Pocket Boxes, 6d., 9d., 18., 18.64. ~ Zine Relaxing Boxes, 9d., 1s., 18. 6d., 28. Nested Chip Boxes, 7d. per ‘four dozen. bs ’ Entomological Pins, See or mixed, 1s., 1s. 6d. ver oz. Pocket Lanterns, 28.6d. to 8s. Sugaring Tin, with brush, 1s. 6d., 2s. Sugaring Mixture, ready for use, — “1s. 9d. per tin. Store Boxes, with ‘camphor cells, 2s. 6d., 48., 5s., 6s. Setting — Boards, flat or oval, 1 in., 6d.; 1¢in., 8d.; 2 in.,10d.; Shin: 1s.; 3}in., 1s. 4d.5 — 4 in., 1s. 6d.; 6 in., 1s. 104.; ‘Complete Set of fourteen Boards, 10s. 6d. Setting — Honses, 9s. 6d., 11s. 6d. ; corked: back, 14s. Zinc Larva Boxes, 9d., 1s., 1s. 6d. Breeding Oage, ‘Os, 6d., 4s., 58., 78.6d. Ooleopterist’s Collecting Bottle, with tube, — | 1s. 6d., 1s. 8d. Botanical Cases, japanned, double tin, 1s. 6d., 28. 9d., 3s. 6d., 4s. 6d. Botanical Paper, 1s. 1d., 1s. 4d., 1s. 9d., 28. 2d., per quire. Tnseot Glazed Oases, Qs. 6d. to 11s. Cement for replacing ‘Antenne, 4d. per bottle. Steel Forceps, — 1s. 6d., 2s., 28.6d, per pair. Cabinet Cork, 7 by 34, best quality, 1s.6d. per dozen sheets. Brass Chloroform Bottle, 2s.6d. Insect Lens, 1s. to 8s. Glass-top and Glass-bottomed Boxes from 1s. per dozen. Zinc Killing Box, 9d., 1s. Pupa Digger, in leather sheath, 1s. 9d. Taxidermist’s Companion, containing most “necessary implements for skinning, 10s. 6d. Sealpels, 1s. 3d.; Scissors, 28. per pair; Egg-drills, 2d., 8d., 94.; Blowpipes, 4d., 6d.; Artificial Eyes for Birds and Animals; Label- lists of British Butterflies, 2d. ; ditto of Birds’ Eggs, 2d., 8d., 6d. ; ditto of Land and Fresh-water Shells, 2d.: Useful Books on Insects, Bees, ke." SILVER PINS for collectors of Micro-Lepidoptera, &e., as well as minute insects of all other families. We stock various sizes and lengths of these Silver Pins, which have certain advantages over the ordinary pins, whether enamelled, black, or silvered or gilt. For instance, insects liable to become greasy, and verdigrisy like Sesiide, &¢c., are best pinned on Silver Pins, which will last much longer. We shall be pleased to send patterns on application. S ROW OR BIO ht OR CURB ANGE Of every description for Inskcrs, Birps’ Kaas, Coins, Microscopical OBsEcts Fossits, &. Oatalogue (100 pp.) sent on application, post free. A LARGE STOCK OF INSECTS AND BIRDS’ EGGS (BRITISH, KUROPEAN, AND EXOTIC). Birds, Mammals, éc., Preserved and Mounted by Firat-claee Workmen. 36, STRAND, W.C., LONDON, ENGLAND. MY NEW REVISED PRICE LIST OF SET BRITISH LEPIDOPTERA now being issued. Write at once if you have not received one. Fine bred Yellow Dominula, 5s. each. Corydon var. Semisyngrapha, 5s. each. Irish specimens (this year’s) Artemis, 2s. 6d, per doz. Minos, 7s. per doz. Hippocrepidis, 5s. per doz. Nai, 3s. 6d. per doz. ; and many others. My Text Book, the ideal work for Collectors; life-history and food-plants of every species, 3s. 9d. post free. Newman’s Electric Lamp, specially designed for collectors, gives 18 hours’ ‘continuous light, 8s. 6d., postage 4d.; new batteries 1s. each, postage 3d. L. W. NEWMAN, F.E.S., BEXLEY, KENT. POR SALE. — lLang’s ‘ Butterflies of . Europe,’ 2 vols. as new (published at £3 18s.), 50s. VTutt's ‘British Lepidoptera,’ 8 vols. (published at £8) ,75s._ Morris’s ‘ British Moths,’ 4 vols., 35s. Ten-drawer Cabinet (Crockett), (cost £6), 75s. Twelve-drawer do. (cost £9), £5 10s... Sixteen-drawer do., £6. Also ‘ sixteen-drawer Cabinet, £6 10s. A. FORD, 36, IRVING ROAD, BOURNEMOUTH. THE ENTOMOLOGIST Vou. XLVII.] FEBRUARY, 1914. (No. 609 A NEW SPECIES OF METANGA FROM FRANCE. By Kenneto J. Morton, F.E.S. In examining a small lot of Trichoptera taken by Dr. Chapman last summer in the Alps of Dauphiné, forwarded by Mr. Lucas, I found four insects, which at first sight I supposed to be Metanea flavipennis, Pict. On confronting these, however, with McLachlan’s figures, I was surprised to find that the details did not agree satisfactorily, and on looking over the material in my collection it was manifest that there were two species, and these rather distinct ones, mixed together, examples from Murgtal (Ris), Silvaplana (Morton), and Carinthia (Klapalek), pertaining to the species described and figured by McLachlan, while others from the Val Bedretto (Ris) were evidently the same as Dr. Chapman’s. I asked Dr. Ris to go over his material, and he confirms my view of the matter. The only explanation of the oversight that can be offered is the identical general appear- ance of the two species, and even with regard to the profile view of the genitalia the similarity is rather remarkable. I propose to describe this hitherto overlooked species as— Metanewa chapman, n. sp. Very similar in appearance to H. flavipennis, Pict. Head, thorax, palpi, legs, and under side of body testaceous, hairs golden ; abdomen above darker. Basal joint of antennz and between the posterior ocelli slightly fuscescent. Spines of legs black. Anterior wings narrow and elongate, pale yellowish, shining neuration concolorous, pubescence of membrane dense, golden Discoidal cell about the same length as its footstalk. Posterior wings whitish, subhyaline with pale veins; first apical cell variable, but narrower at the base than second; second broader, moderately oblique at the base in the direction opposite to the first; third longer than first and second, almost acute at the base; upper branch of cubitus furcating about, or a little beyond the level of the beginning of the discoidal cell. In the male the apex of the abdomen above is rather deeply concave, the posterior margin covered with scattered black tubercles, the side produced into rather long finger-shaped processes whose tips ENTOM.—FEBRUARY, 1914. E 50 THE ENTOMOLOGIST. are very slightly curved downwards, these processes also tuberculate, more densely so towards the apex which thereby becomes black. Superior appendages pale yellow with rounded outline when seen from the side, concave internally. Intermediate appendages viewed from behind, separate, each arising from a narrow stem and spreading out in broad triangular form with three distal projections, the two side ones small, the other long, horn-like, slightly inturned with a small tooth before the apex. Inferior appendages large; from beneath they are close together at the base, diverging slightly, concave internally, rounded at the apex, which is very slightly inturned and clothed internally with short spines and spinous hairs. I am unable satisfactorily to describe the female. Differences probably exist in the genitalia as compared with H. flavipennis, and these could very likely be defined from Canada- balsam preparations. Expanse of wings, male, 19-20 mm.; female, 21 mm. bo Metanea chapmani. 1. Apex of abdomen viewed from above. 2. Apex of abdomen viewed from side. Three males, one female, Lauteret, Alps of Dauphiné (Chapman, July 22nd, August 5th). Also occurs in Val Bed- retto (Ris, September 6th, 1896; July 20th, 1906): Splugen (Ris, July 16th, 1897), uncertain whether from the Swiss or the Italian side, probably the latter; Madonna di San Martino (July 29th and August 1st, 1889, Nageli in Ris coll.). Differs from H. flavipennis, especially in the direction of the blackened processes of the last dorsal segment. These in H. flavipennis are turned to the side almost at right angles to the long axis of the abdomen, whereas in H. chapmani they are nearly parallel, only very slightly out-turned. MeLachlan gives the following localities for H. flavipennis: Dis&ey/zis, Grisons (July 25th, Stainton), Bergun (Zeller), Leuk, Valais (October 2nd, Frey Gessner) Hospice St. Bernard ; Priitigau and Pontresina according to Meyer-Dur; Meyringen (McLachlan, August 16th), Champery, Valais (Haton, August 20th), Samoéns, Savoy (Eaton, September 5th) ; Carinthia (Sep- A NEW SPECIES OF CHIROTHRIPS FROM SOUTH AMERICA. 51 tember, Zeller). Hagen stated that he had it from the Harz, Bavarian Alps, and Styria (?). Ulmer adds Hessen. Supposing it to be the true flavipennis of Pictet, it should occur in the Val d’Illiers, Valais. This list may require revision, as some of these localities may refer to H. chapmani. I found H. flavi- pennis commonly at Silvaplana (July 18th to 25th, 1904); Ris has taken it in the Murgtal (July 27th, 1888), at Cierfs in the Munstertal (July 14th, 29th, 1909); and Klapdélek in Carinthia (July 31st, 1899). A NEW SPECIES OF CHIROTHRIPS (Tuysanoprera) FROM SOUTH AMERICA. By C. B. Wiuurams, B.A., F.E.S. At the beginning of this year I received a small collection of miscellaneous insects from Mr. W. O. Backhouse, taken near Buenos Ayres, in the Argentine Republic, South America. Four genera of Thysanoptera were represented—Chirothrips, Franklin- tella, Physothrips, and Thrips; the Chirothrips, which is a distinct species, is described below; notes on the others are reserved for the present, in the hope of getting further material to elucidate some doubtful points. Gen. CHIROTHRIPS. ) Haliday, Ent. Mag. 1886, iii. p. 444; emend. Uzel, Monog. d. Thysanopt. 1895, p. 79; emend. Hinds, Proc. U.S. Nat. Mus. 1902, xxvi. p. 133. Chirothrips frontalis, sp. nov. Female (macropterous). Measurements.—Head, length 0:15 mm., width (behind the eyes) 0:122 mm.; prothorax, length 0:22 mm., greatest width 0-26 mm. ; pterothorax, length 0°32 mm., width 0°30 mm.; abdomen width 0-35 mm.; wing, length (from basal lobe) 0°80 mm., width (about halfway along) 0:045 mm. Antenne :—segment 1 2 3 4 5 6 ic 8 leneih, (u)~ 14. ; 304, 38 >, 34, 734. 42... 22 16 Width (4). (36. 405,24 24, 2h BO 7. 5 Total length, about 1-4 mm., antenne 0°24 mm. — Colour uniform dark grey brown, fore tibiz and all tarsi a little paler, the third segment of the antenne distinctly lighter. Head (Fig. 1.) longer than wide, produced beyond the eyes into a long prominence more than half as long as the remaining portion of the head. The sides of this at first diverge slightly and then converge rapidly to a rounded point; on the converging portion the antennz are situated. There are no long hairs on the head but several small ones which vary slightly in position and may not be quite sym- metrical. In general they conform to the arrangement shown in the E 2 bo THE ENTOMOLOGIST. figure. Hyes dark and relatively far back. Ocellc distinct, the posterior ones behind the level of the back of the eyes. Crescents red-brown, distinct (in mounted specimens). Mouth cone rounded, reaching about two-fifths across the pro- sternum. Mazillary palps three seg- mented, the basal segment shortest, the apical longest ; four or five sensory hairs at the tip. Labial palps two segmented, the basal segment very short and in- distinct, not much more than a ridge on the labium. Antenne about two-thirds longer than the head; the first segment short and broad, the second much longer and narrower except at the apex where it is produced outwards into a blunt prominence, the third with a distinct pedicel, the fourth and fifth equally long, the sixth the longest, the eighth longer than the seventh. Colour: first and second dark, third clear, fourth to eighth darker but not so dark as the Chirothrips frontalis, sp. nov. first two. An unforked sense-cone on Head and prothorax. the third and fourth segments. Prothorax long, as wide as the head in front but much widened posteriorly, the whole surface of the pronotum finely striated and with a number of minute hairs scattered unsymmetrically over its surface. No long spines at the front angles, two at each hind angle and about six smaller hairs on each side along the hind margin. Pterothorax slightly wider than the prothorax in front, gradually narrowing behind. Legs normal for the genus, fore femora thickened and produced outwards at the base, tibize also thickened. All tarsi (except for a small dark spot at the base of the second segment) and fore tibie lighter than the rest of the legs. Fore wings pale brown, clearer at the base. About twenty (eighteen to twenty-one) spines on the costal vein, the distal ones finer and longer than the proximal; five or six spines at the base of the fore vein and two on its apical half; four, five, or six on the hind vein. The veins are usually very indistinct except near the base of the wings; this varies in different specimens. Hind wings clear, vein indistinguishable. Abdomen normal, hairs on the ninth and tenth segments pale and weak. The ninth segment short, about half as long as the tenth. Described from eleven macropterous females taken near Buenos Ayres, Argentine, South America, in January, 1918, by W. O. Backhouse, probably from a plant (Composite) locally known as ‘‘ cepocaballo.”’ Type in the Hope Department, Oxford University Museum. This species may be easily separated from all others of this genus by the great prolongation of the head beyond the eyes, and also from hamatus, Trybom, obesus, Hinds, crassus, Hinds, A NEW SPECIES OF EURYTOMA FROM QUEENSLAND. 53 and mexicana, Crawford, by having two spines at the hind angle of the prothorax, and from both manicatus, Bagnall, and similis, Bagnall (if these two are really distinct and not forms of the same variable species), by the more slender antenne and relatively longer prothorax. The John Innes Horticultural Institution, Merton, Surrey: January, 1914. A NEW SPECIES. OF EURYTOMA FROM QUEENS- LAND, WHICH LIVES IN THE STEMS OF KUCALYPTUS. By A. A. Grravutt. Tue following species seems phytophagous, since I found it inhabiting short grooves or channels under the bark of young Eucalyptus trees, somewhat after the manner of Scolytide. Where occurring, the stems of the trees were somewhat swollen. When one thinks of it, this species does not seem to differ greatly in habit from the other members of its tribe, which seem to live on galls rather than upon gall-makers. Has the parasitic habit of the Eurytomini been proved ? The genus Bruchophagus would incline one to doubt. Genus Hurytoma, Illiger. Eurytoma picus, n. sp. Black, the legs, tegule and scape rich reddish brown, the hind cox black, the wings hyaline; flagellum brownish yellow, knees and tips of tibie yellow. Propodeum with a rather broad median groove. Venation pale; postmarginal and stigmal veins subequal. Scape obclavate; pedicel a little shorter than funicle 1, which is longest of the funicles, much longer than wide, about twice the length of funicle 5, which is somewhat wider than long, funicle 4 a little longer than wide, funicle 2 subequal to the pedicel. Club with three distinct joints, the antennze 11-jointed. Mandibles tri- dentate. Hind tibie with two spurs. Pronotum with a more or less distinct, obtuse median carina. Punctuation not quite as dense as usual, the cephalic part of scutum densely, transversely lineolated. Male.—Not known. Described from two females taken from short grooves under the bark of young eucalypt trees in the forest, October 16th, 1913. Habitat.—Nelson (Cairns), Queensland. T'ype.-—One of the above specimens on a tag, the head and a hind leg on a slide. In the Queensland Museum, Brisbane. : Magnification 3-inch objective, 1-inch optic, Bausch and iomb. 54 ; THE ENTOMOLOGIST. NEW CENTRAL AMERICAN SYNTOMIDA. By A. E. Gress, F.L.S. Amone the Lepidoptera which I have recently received from British Honduras are two Syntomid moths which appear to be new to science. They were both captured at a small seaport called Punta Gorda in the south of the colony, not far from the frontier of Guatemala. I append descriptions. , Phenicoprocta biformata, n. sp. Head black ; frons blue; palpi orange below ; antennz white at tips; tegule orange with blue spots at base; patigia and thorax orange ; coxe orange-red ; abdomen, first segment blue with paired red stripes, remainder brownish black with dorsal and lateral metallic- green stripes and bluish-green terminal segment ; fore wings hyaline, veins broadly black, oval discoidal spot from costa to lower angle of cell, margins broadly black, widening at apex and on outer margin; hind wings hyaline, with dark borders, widening at apex and tornus. Var. 1. Fore wings scaled, brown-black. Expanse, 30 mm. Habitat.—Punta Gorda, British Honduras, July, 19138. Types in British Museum ; co-types of var. 1 in Mus. Gibbs. Napata cortes, n. sp. Black; tegule and patigia with paired blue-white spots; fore cox white; tibie reddish ; first joints of tarsi white; metathorax with blue-green spot; first segment of abdomen black with a few blue scales and blue-green lateral spots; medial segments blue-green dorsally, with darker transverse bands; large white ventral patch on bagal segments ; remainder of abdomen ventrally and the terminal segments dorsally red; fore wing with bluish spot at base of costa ; small hyaline spot extending across cell near base, and a larger one below it, another in cell near upper angle; a transverse series of four spots beyond cell, one above vein 6 and a smaller one below it, a minute spot above vein 4 and a larger one below it extending almost to vein 3; hind wing with hyaline patch at base; spot near end of cell and extending almost across it; below, fore wing with bluish costal streak, hind wing with blue basal streak above hyaline patch, costa narrowly and apex and outer margin broadly blue. Eixpanse, 41 mm. Habitat.—Punta Gorda, British Honduras, June, 1913. Napata cortes has a general resemblance to N. broadwayi, Schaus., a Trinidad species, but it may be readily distinguished by the large hyaline patch at the base of the hind wing and the red terminal segments of the abdomen. 55 A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. By H. Rownanp-Brown, M.A., F.E.S. (Continued from p. 14.) (v) Basses-Alpes. (a) Allos. As in the case of a previous paper of the series, some quali- fication of title is necessary. Donzel * discovered Allos in 1831. It has received several recent visits from English collectors, myself included, and I have given a short account of a week spent here in August, 1908 (‘ Entomologist, vol. xli. p. 268). However, as I was in this part of the Basses-Alpes at an earlier date than on the occasion of my last visit, or that of the late Mr. J. W. Tutt (‘ Entomologist’s Record,’ vol. xix. pp. 197-199), I trust my experiences may be useful to those who wish to explore the upper valley of the Verdon during the summer months. Allos remains primitive. The motor services, the endless procession of touring cars have left it unperturbed ; and the little Hotel du Midi, where Mdlle. Pascal works so hard for the comfort of her pensionnaires, is as archaic and roughly com- fortable as ever. After a rather disappointing entomological week at Digne— for the universal drought in the lower lands of Provence had burnt up all the green herb—I took train for Thorame-Haute by the familiar narrow-gauge line. Here the alpine motors of the Sud Company pick up, and they are almost as cheap as the former rusty diligence. Between St. André and the starting- point there are doubtless many fine butterfly corners as sug- gested by glimpses caught from the windows of the never- express train. Such a one there is near the station before Thorame, and there I bade farewell to Papilio alexanor—so un- accountably and unusually rare in 1913 in its native haunts at Digne. The drive is pleasant enough by Beauvezer and Colmars, with its narrow medieval streets, through which the motor steers, scraping the stucco from the walls of the overhanging houses—a veritable threading of the needle’s eye. The climb scarcely begins before Colmars, from the gate of which town it is practically all uphill, and as dusty a road as ever provoked the thirst of man and beast. Still, there are several good stretches of collecting ground by the river en route, as I found when, on the hottest day of the year, I descended in quest of Erebia scipio at points indicated by Mr. Powell (‘ Entomologist,’ vol. xli. p. 298). I left Digne at eight o’clock, and reached my destination & ‘Notice Entomologique sur les Environs de Digne et quelques Points des Basses-Alpes,’ par M. Hugues Donzel.. Lyon, 1861. 56 THE ENTOMOLOGIST. about 1.30, and after a late déjeuner at once set off to investi- gate the first length of the classic ‘‘ Route du Lac d’Allos,” where I hoped to capture in good condition some at least of the butterflies over or on the wane when I was here in 1908. With the exception of July 20th and 22nd, the whole of my collecting at Allos was done between the village and the lake. The mule- path mounts steeply from the one street and then more gently, and sometimes between thick hedges, past meadows already harvested, to the first bridge over the Chadoulin stream. On the southward slopes butterflies were generally in evidence, but more distinguished by quantity than by quality. Here on the lavender tufts—this being about the vertical limit of the plant— the males of Hpinephele lycaon were freshly emerged. Of the ‘‘ Blues,” Plebetus argyrognomon predominated, but the beautiful blue female, var. calliopis, Bsdv., of which I had secured a specimen or two at Digne, evidently belongs tv the lower levels and the hotter limestone. A few perfect males of Lycena arion haunted the lavender. Here, also, one warm afternoon towards sunset I picked up a curious aberrant form of Melitea didyma settled to roost. On the under side, while all the black spots and lines remain, the usual tawny markings, notably those of the basal and ante-marginal bands of the hind wings, have almost entirely disappeared, giving a peculiar black-and-white chequered appearance to the insect as it sat motionless on the stalk (=derufata, n. ab.). Hereabouts, too, a low hedge fencing a new-mown field was alive with a diminutive race of Aglaope infausta, both sexes in fine condition, and with them a few Adscita pruni were kicked up from the grass, though neither ‘‘ Burnets”’ nor ‘‘ Foresters ” were at all frequent, and at this point the same remark applies to the Hesperiide, for which I was chiefly on the alert. But, as everywhere else in the south-east this year, Satyrus cordula was abundant; not so Hipparchia semele, though possibly it was still somewhat early for the latter. The only Theclid at all common was 7’. spint, some of the males extraordinarily small, the high Alpes-Maritimes form, as a rule, being of quite the average size. But not one single T’. acacie did I encounter along the line of sloe bushes, where the females were common enough in August, 1908, and where by all rules the males should now have been disporting them- selves. Brenthis amathusia, also not rare near the bridge in that year, was another absentee. Sailing over the willows I saw not a few superb Huvanessa antiopa, with rarer Limenitis camilla and Polygonia c-album. A recent writer has remarked on the moisture-loving pro- pensities of the Camberwell Beauty, and I noticed that it would frequently lie with wings flat and fully extended on the stones facing the sun; and also that very occasionally it joined the A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 57 Lycenid and Hesperiid “drinking clubs” on the surface damp. They never alighted on the mule-droppings so much affested by mountain Lycenide, though P. c-albwm is not above such attrac- tions; and in the spring on the Riviera I have observed that the last-mentioned species is much addicted to the rotten olives left in the orchards from the previous year’s harvest. One Sunday afternoon I crossed the bridge here to explore the path through the pine woods, returning along the water channel which diverts a part of the river to supply the farms above Allos. But these woods and slopes yielded nothing beyond swarms of buzzing and biting flies. The route now ascends sharply on the right bank to the chalets of Champ Richard, and then from a narrow gorge of loose slaty formation debouches on a more open valley, where again the newly constructed path separates from the old, and mounts by zigzags through flowery pastures and occasional larch spinneys. When the sun reaches these upper slopes rather late in the morning there is plenty to occupy atten- tion. Canonympha iphis hardly gives place to C. arcania var. darwiniana; Plebeius argus (egon), much less plentiful than P. argyrognomon, gems with wings of lapis-lazuli the red-gold arnica daisies. Colias phicomone is everywhere, the females just now ina majority. Males of Hrebia stygne, H. goante, and HE. tyndarus var. cassioides (=dromus) cross and re-cross the mule track. The larger Argynnids—A. aglaia and A. niobe (all var. erts)—are already sucking the sweet juices of the purple thistles in company with males of Chrysophanus hippothde var. eurybia and Polyommatus eros. A little higher still H. ewryale affects the woods, and the clearings by the roadside are bright with C. virgauree, P. pheretes (males and females), Parnassius apollo, and occasional E. epiphron var. casstope. About three- quarters of an hour from the last-mentioned bridge a spring empties itself into the torrent; and here over the saxifrage and thick wet moss P. delius was flying at a safe distance from the net. Once more the road crosses the stream, and zigzags- upward through young forests, the nursery of the Maison Forestiére, which now comes into view at a sudden turn. Insects of all orders swarm at this point. The morning is fair and the air delicious with the scent of the many Papilionacez, which make a veritable Field of Cloth of Gold, interwoven with the duller purples of the vetches. A mud-bath hereabouts invites a swarm of P. eros, P. hylas, and Agriades escheri ; Lycéna arion is rare, even more so P. orbitulus, which, common in the Swiss Alps, never seems abundant in the Basses-Alpes and Alpes Maritimes. Hesperia alveus, H. fritillum (= cirsia, Rbr.), H. carthamt, and H. serratule represent the Black-and- White Skippers; Thymelicus lineola and T'. acteon the Brown. To the ‘‘ Coppers’ may now be added C. dorilis var. subalpina 58 THE ENTOMOLOGIST. of both sexes. High up at the back of the Foresters’ House there is a fine piece of rough ground carpeted with soft seeding grasses and alpine flowers. The high fresh wind carries a single Anthocharis simplonia male into my net ; the infrequent Pontia callidice are in rags; but, ascending the last long slope, which ends where the mountains are mirrored in the lake, the Erebias once more claim attention. E. gorge, with occasional ab. erinnys and EH. mnestra, swell the catalogue. Within five minutes of the ridge, on the skrees facing towards Allos, and exactly at the point where the path to the Lacs de l’Encombrette diverges to the right, I discovered on my second expedition the headquarters of H. alecto var. dupon- chet, Obthr., thus obviating the grind up Mont Pélat, where it is reported by Mr. Harold Powell. A more harassing insect to chase and capture Ido not know. To begin with, the favoured ground is always a weary scramble, composed of loose stones and treacherous for the feet, where the most illusive and blackest ‘of all the Hrebias flits restlessly over the rock, or rarely pauses to toy a moment with the scanty yellow Doronicum patches (I cannot find much to differentiate var. duwponcheli from ab. pluto). Added to this, the nature of the locality ensures for every perfect imago a half-dozen in tatters, while crumpling and failure of wing-pigment is of frequent occurrence. The females were few in number; in vain I watched for one to alight and oviposit and clear up the still outstanding mystery of the food-plant of the species. Below the path and on the rock-strewn ‘‘ pelouse’’ that falls to the mouth of the subterranean stream draining the still invisible Lac d’Allos, Melitea varia is common with C. phico- mone, a8 well as the small Erebias. Here, also, I took a couple of wasted H. cacalie, and even more passés H. malvoides, Klw. and Kdw. (= fritillum, Rbr.)—the Dromio of H. malve—for the specific confirmation of which I am much indebted to Professor Reverdin, to whom the three or four examples caught at a single sweep of the net were submitted. I do not doubt that earlier in the season this Skipper occurs in most suitable localities throughout the lower Basses-Alpes. Allos, however, may now be added authoritatively to Professor Reverdin’s list of French localities published in his masterly treatise on the two species (Bull. Soc. Lépid. Genéve, vol. ii. fas. 2, p. 78, 1911). Through- out the valley, from Champ Richard upwards, H. serratule was frequent ; and I have from the same region in my collection a few Hesperiids, which seem to me to be intermediates between H, bellierit, Obthr., and the var. foulquieri, which M. Oberthur retains provisionally under alveus, but will, I think, some day not far off be found nearer associated with belliert. I was surprised to find so few butterflies on the slopes lead- ing down to the matchless lakelet, where in 1908 insects were A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 59 fairly plentiful. Except a few shabby Cassioides and the ubiquitous C. phicomone, there was nothing to tempt me from the rock behind which, and sheltered from the keen wind, I dis- posed of my lunch. So I devoted the greater part of the time on each occasion to Alecto-Duponcheli. July 22nd, the hottest day of the month, I spent working down the Verdon river-bed, which, in the customary way of Alpine torrent streams, breaks up into many subsidiary chan- nels, leaving broad stony islets covered with dwarf willow, lavender, Epilobium angustiflorum, great clumps of Astragalus alpinus (?), and tangled vetches, with occasional tufts of wild thyme. The lavender was especially affected by A. escheri, P. argyrognomon, and females of C. alciphron var. gordius, the latter in poor condition, while Anthrocera fausta gleamed ver- million-winged in equal abundance with A. carniolica. The steep cliffs of the right bank, however, disclosed no LE. scipio, as I had hoped, after a long search for a ford waded knee-deep through spring-cold water. A rare pool for trout at all events; and trout is the picce de résistance of every meal in these delec- table mountains. Returning to the causeway at the end of the long poplar avenue, which extends for a mile or so, the valley once more opens out, and on the left bank, where the old road follows the course of the river, there is a sun-burnt stretch of waste land with sparse berberis bushes, mullein, and again some fine lavender in full bloom. IT’. acteon, A. thersites and Issoria lathonia were the principal visitors; on the dusty upper road Satyrus circe was flying with S. alcyone, but very little besides, and it was not until I was well in sight of Colmars itself that I could get a draught of drinking water at a hospitable farm- house, in the garden of which the ripe red currants hung in ‘luscious clusters. The neighbouring lucerne fields were gay with Colias edusa and C. hyale, but so great was the heat of the afternoon that at two o'clock I boarded the P.L.M. motor and was quickly rushed back to Allog. Above the village and right up to the Col there is very little promising ground. The slopes on this side are mostly disafforested and grazed close. I tried not to think that the few Erebias I saw from the car, when on my journey of the 24th to Barcelonnette, were H. scipio. I am now sure they were not—only stygne. I have been asked where, in my Continental wanderings, I have found butterflies in the greatest profusion. It is not an easy question to answer, for ‘‘ distance lends enchantment to the view ’’ of most entomologists when the time arrives to survey in retrospect the happy hunting grounds of the past. I am inclined to think that certain stages of the road to the Lac d’Allos I have attempted to describe come nearest to El Dorado. Then follow the Kaux Thermales valley at Digne, in June; 60 THE ENTOMOLOGIST. St. Martin-Vésubie, or the Ganter Bridge below Berisal, in mid-July ; with a far-away April vision of Hadrian’s Villa at Tivoli, with its winged legions ‘‘ fleeting the time carelessly as in Arcady.’”’ In point of numbers only, some secluded spots in the Chiltern Hills have provided almost as cheerful an abundance. Last year (1913) the Basses-Alpes were at least blessed with a summer of sunshine and butterflies in striking contrast to the melancholy conditions and the meagre bags reported from Switzerland and Central Europe generally. (To be continued.) SOME NOTES ON THE LEPIDOPTERA OF LA SAINTE BAUME, VAR, 8S. FRANCE. By Rev. F. E. Lows, M.A., F.E.S. II. Tue Morus. TuoucHu Switzerland can never be without interest, after many years’ experience of it the collector begins to crave for new ground. If Norway does not appeal to him, he probably decides to explore as far south as the limits of his time and purse permit. This was my case in the summer of 1912—but —Where to go? was the question. I wisely consulted Mr. Rowland-Brown, to every entomologist a veritable ‘‘ Baedeker ”’ for France; who, after dismissing my suggestion of Thorenc— of which he had received no reports—proposed La Ste. Baume as being a centre well spoken of by French, and little known to English, collectors. Thither I went therefore, and spent such an interesting ten days that I returned again for a slightly longer visit this year. I had sent a selection of my 1912 cap- tures for identification to Mr. Prout, who is always kind enough to help me out of any difficulties with geometers. It was an unexpected pleasure to hear from him that I had fallen upon a very good thing, viz., Acidalia determinata. He wrote: ‘‘ You have some interesting forms, and 4. determinata was quite a surprise. I had never even seen the species until a few weeks ago, when Pungler very kindly sent a valuable box of Acidalids for my inspection . . . and included a pair of this species, one from Calabria and one from Taurus. Where exactly is Ste. Baume? It will surely be a new locality for this insect. If you ever visit this place again, work for a series.” Here was sufficient incentive, and this year my wife and I returned with ardour to the search, and were successful in getting together about thirty specimens. Perhaps it is early days to express an NOTES ON THE LEPIDOPTERA OF LA SAINTE BAUME. 61 Opinion, but it appears to be very local even where it exists.* We found it restricted to quite a small space on the edge of the wood which borders the north-east corner of the plateau before beginning the descent to Nans. But its allies, A. macilentaria and A. litigiosaria, are fairly commonly distributed over all the neighbourhood, more particularly the former. From neither of these could I pretend to distinguish it in flight; but A. macilen- taria, which is most like it on the upper side, is readily distin- guished when caught by its dark strongly-marked under side. A. determinata is not an active insect and is easily overlooked, as it seems rarely to fly unless disturbed; but like other ** waves,” it is fond of lying spread out on a leaf—not, I think, in the full sun, but rather close to the ground, and where longer branches above afford a slight shade. In our experience, it was always driven out of little stunted oak bushes; whether it had any closer connection with these than the fact they provided a pleasant resting-place I cannot venture to suggest. From the list of captures appended it will be seen that the Acidalids proved a strong and interesting family in this region, while the Larentids were remarkably few and ordinary. The Zygenids provided variety, but with the exception of Z. angelice and Z. lonicere coud hardly be considered numerous. That almost most beautiful ‘‘burnet” of all, 7. lavandule, appeared only separately on the road to Nans; but on crossing the Col de Bretagne, I found a large colony feasting on the flowers of “hemp agrimony,” or a plant like it, growing in a hollow by the side of the Gémenos road. This, I think, is an unusual occurrence, for at Bondol, where Z. lavandule was more com- mon, I always took it singly and generally on the wing. Z. erythus, on the contrary, has the burnet-habit of congregating, and was seldom seen alone, but had a restricted headquarters of its own; and gave its attentions to a tall wiry scabious with little wizened flowers, which would have been justly despised in any better watered land. Probably the more active habits of lavandule accounted for a difficulty in getting good specimens. It seems also to be a slightly earlier species. The most remark- able feature in ‘“‘ moth-land,” perhaps, was the extraordinary quantity of three small species in the herbage of the plain of Plan d’Aup. I have already remarked in a former paper on the abundance of Rusticus egon. But even more wonderful—espe- cially in 1912—was the enormous number of Acidalia sericeata ‘and A. decorata, disturbed in walking over the plateau; and with them almost as many Crambus craterellus —the only Crambus observed, with the exception of two or three C. cwmellus. Among the “ pugs,’ Mr. Prout has praise for T’ephroclystia * An indirect but suggestive token of the rarity of A. determinata, in collections may be gathered from the fact that it is not offered for sale in either the Staudinger, Bang-Haas, or Bartel price-lists. 62, THE ENTOMOLOGIST. allionia and T. ultimaria. The handsome Ortholitha meniata was very common in the woods and at light; and ascending the wooded path to the Col de Bretagne Minoa murinata, in spite of its small size, was a prominent feature. The Noctue and the Tephroclystie were all taken at light, the other families nearly all netted in the daytime, the chief exceptions being Acidalia virgularia var. australis, A. submutata, Ephyra pupillaria, Boarmia solieraria (one male), Trephonia sepiaria (two), Hylo- phila bicolorana, Eromene bella, which were attracted by light. Besides Mr. Prout, I am also under obligations to Dr. Chapman for naming certain specimens and to Mr. Bethune- Baker for help with the Zygenids. It is impossible to foresee what system of nomenclature this paper may represent after it has passed the Editor’s hands; but in making my list I have followed the Staudinger-Rebelschen Catalog. 1901. As Mons. Culot says in his preface to vol. ii. of ‘ Noctuelles d’Europe’: ‘‘Le catalogue que j’ai pris pour guide, parce qu’il est le plus répandu.” I hesitate to add with him: ‘ Et non parce quwil représente une classification rationnelle.’’ Such criticism is for the ever-conflicting experts. We spent two or three days at Bondol on the sea coast, hunting Zygena erythus, While there I took a few rather good moths at light, and as Bondol is not far distant from La Ste. Baume, I have added these captures as a separate note. Heterocera oF Ste. Baume anp Nans. SpHincipz.—Macroglossa stellatarum, Deilephila euphorhne, Hemaris fuciformis. LyMANTRIIDE.—Orgyia trigotephras (var. corsica ?). Lastocamprpm.-—Malacosoma neustria. DRrepPaANipz#.—Drepana binaria (one female). Noctuip™.—Acronycta rumicis (dark), Dianthecia compta, Caradrina exigua, Leucania scirpi, Thalpochares polygramma, T. purpurina, T. scitula, Rivula sericealis, Prothymnia viridania, Hemerosia renalis, Catocala conversa, C. nymphagoga, Apopestes dilucida, Huclidia glyphica. GEOMETRIDH.—A plasta ononaria, Geometra vernaria, Nemoria viridata, Acidalia ochrata, A. macilentaria, A. determinata, A. rufaria, A. litigiosaria, A. sericeata, A. moniliata, A. virgularia var. australis, A. circuitaria (two), A. trigeminata, A. dilutaria, A. degeneraria, A. inornata, A. aversata, A. rubiginata, A. mar- ginepunctata, A. submutata, A. imitata, A. decorata, HEphyra pupillaria, and var. gyrata, E. linearia (trilinearia, Bkh.), Rhodo- strophia vibicaria, R. calabraria and ab. tabidaria. LARENTINE.—Sterrha sacraria, Ortholitha meniata, Minoa murinata (euphorbiata), Larentia fulvata (one), L. bilineata (one), Tephroclystia (Hupithecia) allionia, T. breviculata, T. ultimaria, T’. oblongata, T’. pumilata, Rumia luteata (one). NOTES ON THE DRAGONFLY SEASON oF 1918. 63 Boarmunm.—Boarmia solieraria, Trephonia sepiaria, Hubolia murinaria. Cympipm.—Hylophila bicolorana. Hererocynipz.—Heterogynis penella. Lirnosun®.—Lithosia lurideola, L. complana, L. caniola. YyvamNIDE.—Zygena scabiose var. orion, Z. sarpedon and var. vernetensis, Z. achillee, Z. lonicere and var. ochsenheimert, Z. transalpina, Z. angelice, Z. lavandule and var. consobrina, Z. hilaris var. ononidis (one). Ino (apscrta), I. globularie, Dyspessa ulula. Pyrauips, &ce.—Crambus craterellus, C. cumellus, Hromene bella, Pyraustra sanguinalis, P. purpuralis, P. funebris (octo- maculata), P. cingulata, Titanio polinalis, Evergestis sophialis, Salebria palumbella. At Bonpou. Zygena erythus, Z. filipendule; and at light, Semiothisa (Macaria) estimaria, Gnophos mucidaria, Hublemma_ suava, E. jucunda, Pseudophia illunaris. NOTES ON THE DRAGONFLY SEASON OF 1913. By F. W. & H. Campion. THE most interesting dragonfly seen by us during the present year was a female of Somatochlora metallica taken in Surrey on June 8th (H. J. Watts). The capture was made in the same locality as that which furnished the male obtained by the same entomologist on June 26th, 1910 (Entom. xliv. p. 238). When first taken, Mr. Watts tells us, this female was in somewhat teneral condition, but it was kept alive for a few days and deve- loped into a very fine specimen. When we saw the insect, after it had left the setting-board, the wings, including the ptero- stigmata, were of a beautiful amber, the colour being richest in the region of the costa. In a fully adult female from Guisachan, taken in August, 1899, by Mr. J. J. F. X. King, with which we compared the Surrey specimen, the pterostigmata are pinkish- red, and the wings are only slightly tinged with brown. Well authenticated records for this species from any part of Great Britain south of the Grampians are still very few, and its ~ occurrence in Sussex in 1908 came to Odonatists as quite a surprise. During the last week in May Mr. R. South visited the New Forest, and obtained at Brockenhurst (May 380th) Calopteryx virgo, Pyrrhosoma nymphula, and Agrion puella. From the same locality we also received, through the kindness of Mr. South, Platycnemis pennipes, Pyrrhosoma tenellum, Orthetrum cerulescens, 64 THE ENTOMOLOGIST. and Sympetrum striolatum, all dated July 16th, as well as Enallagma cyathigerum and Erythromma naias, likewise taken in July. Furthermore, Mr. South was good enough to give us Enallagma cyathigerum, male, caught by himself at the Black Pond, Surrey, on August 13th. From the Eastbourne district Mr. Harold Bosley kindly sent us A. puella (two teneral males, near Pevensey, May 24th), A. pulchellum (a teneral pair, near Pevensey, May 24th; two pairs, Eastbourne Marshes, June 14th), and Ischnura elegans (two males, Eastbourne Marshes, June 14th). At Westcliff, Essex, Mr. A. Luvoni recorded P. nymphula and Libellula depressa on May 25th, I. elegans on May 31st, and A. puella on June Ist. During June we re-visited our old Huntingdonshire localities, and, among other species, again met with Libellula fulva (near Huntingdon, June 16th and 18th), L. quadrimaculata and Brachy- tron hafniense (near Ramsey, June 17th), Calopteryx splendens (near Huntingdon, June 12th), and Hrythromma naias (near Huntingdon, June 21st). Finally,.Dr. F. F. Laidlaw has favoured us with a list of the species observed by him in Devonshire during 1913. His report, which is in the following terms, relates to Uffculme, except in the case of those records for which other localities are specially mentioned :— ‘‘The earliest Odonate met with was Pyrrhosoma nymphula. I saw a female specimen on May 11th, and the species was flying in some numbers the next day. Calopteryx virgo put in an appearance nearly a month later than it did last year. I observed the first specimen, a teneral male, on May 28rd, but the species was very abundant by May 28th. On the last-named date I saw very many specimens, and the insect seemed to me to be much more numerous than it was last year. Hxactly the opposite was the case with C. splendens, which was first noticed on June 15th, but which was never so abundant as in 1912 or so numerous as its congener. Libellula depressa occurred on May 26th at Sheldon. Brachytron hafniense was taken at Burlescombe by Mr. H. Pearse on May 27th. Ireceived a female of B. hafniense from near Langport, in Somerset, and a female of Agrion pul- chellum, also from Langport, through the kindness of Miss D. Wright (June 4th). Other records are Agrion puella (Willand, June 16th), Hnallagma cyathigerum (Willand, June 20th), Cordule- gaster annulatus (September 7th and 19th) and Sympetrum striolatum, males, (Burlescombe, September 21st and 28th). On June 27th I saw an Auschnid chased in a playful way by a sparrow, which, however, it easily evaded.” 58, Ranelagh Road, Ealing, W.: Dec. 26th, 1913. 65 FORFICULA AURICULARIA. By H. H. Brinnuey. Forficula auricularia (slightly magnified). Tue individuals in the photograph reproduced are a female and two males, the latter being as regards length of callipers “high” and “‘low,” following the terminology of Bateson (Proc. Zool. Soc. London, Noy. 15, 1892, p. 585). They were obtained in September, 1918, on the uninhabited islet of Rosevear in the Scillies, situated about two miles east of the Bishop Rock. This islet swarms with earwigs which are mostly large bodied, while the ‘‘ high ’’ male is much commoner than the ‘‘low.’”’ Rosevear was inhabited from 1850 to 1858 by the workmen employed to build the present Bishop Lighthouse. Is it possible that the remarkable abundance of earwigs, on an islet whose features are mainly masses of granite and a vegetation of sea-pink and giant mallow, is related to this human settlement of half a century ago? On Round Island, the northernmost islet of the Scilly eroup, earwigs are also very numerous and seem to feed chiefly on the kitchen refuse thrown ‘‘ over cliff’’ by the light keepers, the only human inhabitants. The specimen illustrated has callipers 12°25 mm. in length, and thus markedly exceeds that taken by Mr. P. M. Bright at Freshwater, Isle of Wight, in 1910, and illustrated in the ‘Entomologist,’ June, 1911, p. 209. In Mr. Bateson’s collection of 1892 in the Farn Islands six specimens had callipers 9°0 mm. long, and in 1907 and 1908 I obtained four from the same locality with callipers 8°75 mm. In a collection made on Round Island in 1911 I found thirty-four males with callipers 10 mm. or more, among which the highest had the value 11°0 mm, ENTOM.—FEBRUARY, 1914. F 66 THE ENTOMOLOGIST. Till I measured the Rosevear specimen the above was the largest ‘high’ male or var. forcipata known to me. _ It is probable that Mr. Bright’s Freshwater specimen, on my method of measurement, has callipers slightly more than 10 mm., because they were apparently measured in situ. The latter method is quite unsatisfactory when a large series is being measured to ascertain the amount of variation, because the degree to which the bases of the callipers are telescoped into the last abdominal segment differs in a series of individuals. So I always extract the callipers to expose the small process, a kind of condyle, which is situated on the external margin of the calliper and is usually only just hidden by the last abdominal tergum. The callipers are then laid on squared mm. paper and measured in a straight line from the ‘‘condyle”’ to the distal extremity, the curvature being disregarded. This is permissible, because, though ‘‘high’’ males possess straighter callipers than do the ‘‘low,” as the correlation is constant the curve of variation is not vitiated. Unfortunately the body of the Rosevear ‘“‘high” male was damaged either at capture or in subsequent transport in spirit, so that it could not be set symmetrically for photographing. I have not yet measured the other Rosevear males, but there are many which closely approach the example illustrated. Taken altogether they seem to possess in both body and callipers the largest average dimensions of any collection from one locality I have seen. Zoological Laboratory, Cambridge: December, 1913. THE NEUROPTERA OF NOTTINGHAMSHIRE. By J. We Care, M.A,de.s.; 2 .G.8: (Professor of Biology, University College, Nottingham.) THE distribution of these insects in Britain is still so in- sufficiently worked out that a list of the species recently taken in Nottinghamshire may be of some use. With few exceptions all have been collected during 1912-13 by myself, and every specimen recorded has been identified or confirmed by Mr. Kenneth J. Morton, to whom I am greatly indebted for much generous assistance with this and other groups of Neuropteroid insects. Srauip# (Alder-flies). Sialas lutarca, Linn.—By rivers, canals, and ponds everywhere. S. fuliginosa, Pict.—EHaton, near Retford, May 29th, 1901. RapuHipup# (Snake-flies). Raphidia notata, Fab.—Epperstone Park, May 12th and June THE NEUROPTERA OF NOTTINGHAMSHIRE. 67 20th, 1912 (J. W. Saunt); Sherwood Forest, near Edwinstowe, June 12th, 1912. R. xanthostigma, Schum.—Sherwood Forest, near Edwinstowe, several, June 10th—14th, 1912; also at Langford Moor, near Newark, June, 1904. HeMEROBIIDe (Brown Lacewings). Sisyra fuscata, Fab.—Sherwood Forest, near Ollerton, July, 1912. Hemerobius elegans, Steph.—Burton Joyce, July 9th, 1904. H. micans, Oliv—Thorney, August,’ 1913 (L. A. Carr); Epper- stone Park, September 6th, 1913. H. nitidulus, Fab.—Epperstone Park, September 6th, 1913. H. humuli, Linn.—Nether Langwith, August 19th, 1912; West Leake, May 27th, 1913; Epperstone Park, September 6th, 1913. H. lutescens, Fab.—Common. Nottingham; East and West Leake; Kirkby-in-Ashfield ; Epperstone Park; Thorney; Sherwood Forest, &c.; dates varying from May 17th to September 24th. H. orotypus, Walleng. Aspley Woods, near Nottingham, August 9th, 1912; Sherwood Forest, near Edwinstowe, September 25th, 1913. H. nervosus, Fab.—Epperstone Park, September 6th, 1913. H. subnebulosus, Steph.— Everywhere common. Taken con- tinuously from April 24th to September 12th. : ; H. quadrifasciatus, Reut.—Sherwood Forest, near Edwinstowe, June 10th—14th, 1912 (L. A. Cary). Micromus paganus, Linn.—Aspley Woods, June 28th and July 26th, 1912; Kirkby-in-Ashfield, June 28th, 1913. M. angulatus, Steph. — Sherwood Forest, near HEdwinstowe, September 25th, 1913. CurysoPip& (Green Lacewings). Chrysopa flava, Scop.—Holme Pierrepont, June 1st, 1912 (F. M. Robinson); Caythorpe, September, 1912; Kirkby-in-Ashfield, June 28th, 1913. C. alba, Linn.—Epperstone Park, June 22nd, 1913 (J. W. Saunt). C. tenella, Schrd.—Bulwell Hall Park, July 8th, 1912. C. septempunctata, Wesm.— Ollerton, Sherwood Forest, July, 1912; Nottingham, common on hawthorn trees in my garden and elsewhere in the city. C. prasina, Ramb.—Sherwood Forest, near Edwinstowe, August 1st, 1911. C. ventralis, Curt.—Nottingham, 1912 (J. W. Saunt). C. phyllochroma, Wesm.—East Leake, June 18th, 1912. C. perla, Linn.—-Budby-carr, Sherwood Forest, several, July 9th, 1913; Worksop, 1913 (J. E. Hodding); Cotgrave, June 21st, 1913 (Saunt). CoNIOPTERYGID. Conwentzia psociformis, Curt. — Nottingham, May 27th, 1913; Warsop, July 14th, 1913. Semidalis aleyrodifornus, Steph.—Nottingham, 1901; East Leake, July 3rd, 1911; Upton, near Southwell, beaten from ash and oak, June 30th, 1913; Fiskerton, from Pyrus malus, July 25th, 1913, 68 THE ENTOMOLOGIST. Coniopteryx tinetformis, Steph. — Thorney, August 15th—19th, 1913 (L. A. Carr). PANoRPIDH (Scorpion-flies). Panorpa communts, Linn.—Common throughout the county, June 12th—August 24th, 1913. P. cognata, Ramb.—Bulwell, July 6th, 1912 (Ff. M. Robinson) ; Thorney, August 15th-19th, 1918, two specimens (L. A. Carr); near Newbound Mill, Teversall, August 3rd, 1912. P. germanica, Linn.—Common everywhere in Notts; taken from May 11th to September 12th. [In addition to those above mentioned, the following species have been recorded for Nottinghamshire :—- Hemerobius inconspicuus, MeLach.—Clumber Park, 1908 (Lady Robinson). H. stigma, Steph.—Worksop, 1904 (Lady Robinson). H. atrifrons, McLach. and H. concinnus, Steph.— Worksop, 1908 (Lady Robinson). Chrysopa vulgaris, Schrd.—South Leverton (Rev. A. Thornley) ; Shireoaks, Worksop (J. T. Houghton). Nothochrysa capitata, Fab.—Sherwood Forest (H. Donisthorpe).] A NEW GENUS OF TRYDYMINE MISCOGASTERIDAG (HYMENOPTERA CHALCIDOIDEA). By A. A. GiIrauut. TRYDYMINI. H}PITEROBIA, N. gen. Female. —Agreeing with Terobia, Foerster, but the scutellum with a distinct cross suture before apex, and the marginal vein is fully twice the length of the stigmal, which is distinctly shorter than the postmarginal. Both mandibles flattened, distinctly 4-dentate. Abdo- men conic-ovate, keeled beneath, the second segment longest, occupy- ing about a fifth of the surface, its caudal margin with a slight notch at the meson; abdomen somewhat longer than the rest of the body. Antenne with the first ring-joint very short, inserted below the middle of the face but somewhat above the ventral ends of the eyes. Lateral margins of propodeum carinated, but true lateral carine absent, the median carina distinct, not very long, complete. Spiracle small, round, central (i.e. midway between cephalic and caudal margins, far from cephalic margin). Parapsidal furrows deep. Male.—Not known. Type.—The following species. Epiterobia reticulatithorax, n. sp. Female—Length, 1:15 mm. Dark coppery green, the wings hyaline, the thorax finely reticulated, the lines not raised, smooth on scutellum caudad of cross-suture; propodeum glabrous. Coxe con- NOTES AND OBSERVATIONS. 69 colorous, the femora also, the knees, tibiz and tarsi pale. Mandibles somewhat like an outspread hand with the last finger-joints turned down and the thumb hidden. Antennz pale yellowish, the pedicel above at base and the club dusky. Club somewhat enlarged; funicle joints subglobular, wider than long, increasing somewhat in size, distad, but always shorter than the pedicel, which is a little longer than wide. Club apparently with a minute apical fourth joint (excluding this, antenne 13-jointed with two ring joints). Described from one female captured by sweeping in forest, December 2nd, 1912 (A. P. Dodd). Habitat.—Nelson (Cairns), Queensland. Type.—The above specimen on a tag, the head and a hind leg on a slide. In the Queensland Museum, Brisbane. The species was described with a Bausch and Lomb micro- scope, ?-inch objective, 1-inch optic. NOTES AND OBSERVATIONS. Do Hovuss-Fiirs Hypernate?—It is commonly believed that the persistence of Musca domestica from one season to another is ensured by the survival of a certain number of fertilized females, which pass through the winter usually in a dormant condition in nooks and crannies in houses, and become the mothers of the earliest broods of the following year. In spite, however, of the large amount of attention bestowed upon the House-fly during the last few years, owing to the recognition of its importance as a disease-carrier, definite proof that the insect hybernates in the perfect state is still wanting; indeed, Dr. Henry Skinner, as the result of an observation made by him last March at Philadelphia, U.S.A., has recently an- swered the question at the head of this note by stating that: ‘“‘House-flies pass the winter in the pupal stage and in no other way” (‘Entomological News,’ vol. xxiv, No. 7, July, 1913, p. 304). This conclusion, it should be noted, is directly at variance with results obtained in this country by both Newstead and Jepson. Did we possess exact knowledge of what happens to the House- fly in the interval that elapses between the disappearance of the last belated stragglers in November and December, and the sporadic invasion of our dwellings in the following June by the earliest skirmishers of the season, it is obvious that we might be able to deal more effectually with an ever-recurring menace to the public health. This point has not been overlooked in the investigations upon “ Flies as Carriers of Infection,’ which for several years past have been carried on by the Local Government Board, under the direction of Dr. 5. Monckton Copeman, F.R.S., but hitherto the results have been purely negative. Hybernating flies belonging to several species have been found in attics and elsewhere, but upon careful exami- nation it was found that these did not include a single House-fly. In this matter the importance of accurate determination of species is obvious, and the object of the present note is to enlist during the 70 THE ENTOMOLOGIST. present winter the sympathetic aid of readers of this Journal, in securing and forwarding for identification collections of hybernating flies. Such flies may be looked for in attics and other unoccupied rooms, in chinks and crannies in living rooms, such as the space between a shutter or a loose piece of wall-paper and the wall, and in stables, barns and other outbuildings close to houses. Every con- signment of flies so collected, if forwarded (with label stating place and date of capture) either to Dr. S. Monckton Copeman, F.R.S., Local Government Board, Whitehall, S.W., or to the writer, will be gratefully and promptly acknowledged and investigated. The flies should be placed, just as they are, in a small tin box or wide-mouthed bottle, well protected by soft wrapping and despatched by parcel post. Such parcels, if sent to Dr. Copeman at the Local Government Board, and marked * O.H.M.S.,” need not be stamped.—Ernest H. AustEN ; British Museum (Natural History), Cromwell Road, London, S.W., January 10th, 1914. Notes From SaLtcomBe, AuGcust, 1913.—Colias edusa was first seen on the Kingsbridge Road on August 10th after church, and was apparently a freshly emerged male. There was a large clover field a short distance away, but although the field was visited on all suitable occasions for several days, and at intervals until the end of the month, not a single other specimen was seen in that neighbour- hood. On August 15th a male appeared on the tennis courts and was promptly acquired with the help of a racquet. The same day my wife discovered the species flying quite freely in a steep stubby field on the Portlemouth side of the harbour. A few specimens were generally to be found there in sunshine for the next ten days, when they became scarcer. It was a great pleasure to find Vanessa io commoner than I have seen it for thirty years. It occurred almost everywhere, but swarmed in some of the ravines on the Bolt, where at least half a dozen on one occasion were feeding on an inaccessible clump of valerian, its chief attraction. No doubt these were the imagines from the larve noted as common at Salcombe by Mr. R. M. Prideaux on July 1st. V. zo was in the pink of condition, a large percentage being absolutely perfect and very fine. Pyrameis cardut were very common in the clover field and in good condition. P. atalanta appeared frequently towards the end of the month. On August 19th a number were flying on the sandhills at Hope, where they were greatly attracted by the Hryngiwm, then in full bloom. Argynnis paphia was about over, but a few were seen in the Courtenay Woods and on the Bolt. Satyrus semele was common on the barer part of Bolt Head, but was worn, and only four perfect specimens was taken. Pararge egeria was numerous in all suitable localities and in all conditions. Pararge megera and EH pinephele tithonus swarmed on the banks at the sides of the high roads, but both were dilapidated. Canonympha pamphilus and Chrysophanus phleas were present in some numbers in the edusa field and less commonly elsewhere. Lycena astrarche occurred in one corner of the same field, but was confined to a space of about fifteen yards square, and it was met with nowhere else. J. ecarus was the only blue seen, and not a single skipper or hairstreak was noted. ad NOTES AND OBSERVATIONS. rial! Eupithecia larvee were common on Galiwm, Artemisia, and Senecio. Dusking was not very successful, and sugaring on the cliffs was unproductive during the greater part of the month. By far the most common insect at sugar in the Courtenay Woods was Amphi- pyra pyramidea, which came freely during the last days of our visit. On one occasion five were successfully boxed from one patch. Four Lymantria monacha came to the lantern one night in a pine wood. The flowers of Senecio near the sea were not worth working, although in 1912 at Sutton-on-Sea common species swarmed on it. —G. Hanson Sate; Littleover House, Littleover, Derby. Morus CASUALLY PASSING MORE THAN A YEAR IN THE PUPAL Srate.—Mr. Robert Lawson’s note upon some examples of Bzston hirtaria, which spent nearly three years as pupz with him (Entom. xlvi. p. 332), interests me much, as I have long suspected that to something of this kind may perhaps be attributed the extra abundance of certain insects in certain years so often remarked upon. I have had several species of caterpillars from time to time in my rearing cages, that have missed the usual time of emergence, and duly turned to imagines in the following year; but will, mean- while, only mention one case which is curiously like that referred to by Mr. Lawson. In August and September, 1888, larvee of Notodonta ziczac happened to be unusually numerous round Berwick-on-Tweed, and a number of them were transferred to the breeding cages, Most of these duly emerged in the following year, from May 22nd up to July 14th, but a few pupe remained alive in the cage till 1891, when one perfect insect emerged from one of them on July 18th, none of the remainder being then alive. But the point I particularly wish to emphasize is that, although upon the poplar trees from which the larvae had been gathered in 1888, no ziczac caterpillars appeared in either 1889 or 1890, in the autumn of 1891 they were again numerous. It might, of course, have been no more than a coincidence, but it strongly suggested some conditions, climatic or otherwise, especially favourable to the species, and common to the years 1888 and 1891; as well as that certain of the wild insects might also have passed the intervening two summers in the pupal state.— GrorGE Bortam; Alston, Cumberland. LITHOSTEGE GRISEATA SECOND Broop.—I had a few larve of this species last year which duly pupated, and I was much surprised to find on looking at the cages in September that five moths had emerged (two males and three females). They had evidently paired and laid, as there were some old eggshells about, but the larvee had of course perished. This may account for the scarcity of the species some seasons, as if there is a second emergence the resulting larve would surely perish, as the S¢symbriwm would be dying and the seeds fallen before the larve could feed up.—H. M. Eprtstren; Forty Hill, Enfield. “THE VERRALL SuPPER.”—No entomological event of the year, as we have before asserted, is of greater social interest or of more value for founding friendships than the “ Verrall’” supper, which annually perpetuates the memory of those given by the late G. H. Verrall and that of the donor. In 1913 the number of guests was 72 THE ENTOMOLOGIST. but little under one hundred, but on January 20th of the present year that record was broken, as one hundred and three then sat down to supper. Among those present were Adkin, Andrews, Arrow, Atmore, Black, Bateson, Bethune-Baker, Bouskill, Burr, Bagnell, Bacot, Bethel, Blair, Butler, Buxton, G. C. and H. G. Champion, Chapman, Collin, Cameron, Campion, Cockayne, Crawley, Dixey, Donisthorpe, Druce, Durrant, Stanley and F. W. Edwards, Elliott, Frohawk, Frisby, Fryer, Gahan, Gibbs, Hall, Harmer, Hodge, Image, O. E. and J. O. Janson, Jackson, Jenkinson, Jennings, Jones, Joy, Jordan, Joseph, Lloyd, Lucas, Main, Meade- Waldo, Mitford, Morley, ~ Morice, Nurse, Nicholson, Porritt, Poulton, Prout, W. Rothschild, Rowland-Brown, Riley, W. EH. Sharp, Sich, Skinner, Smith, Step, Tomlin, Tonge, Turner, Wainwright, Walker, C. O. Waterhouse, and Wheeler. A DraGonFruy at SeA.—The dragonfly taken at sea mentioned on p. 39 has been kindly identified for me by Mr. W. J. Lucas. It is a fully coloured male of Sympetruwm scoticum. It was taken between Revel and Helsingfors, the former name being previously misprinted as “ Kevel.’”—Joun B. Hicks; Stoneleigh, Hlmfield Road, Bromley, Kent, Jan. 8th, 1914. Errata.—Page 27, line 13 from bottom, delete ‘“ croricnus.” Page 36, line 10, for ‘‘samoensis”’ read “samoaensis.” Page 37, line 19, for “no posterior” read ‘‘two posterior”; line 24, for ‘‘ Thorp” read « Theobald.” SOCIETIES. LANCASHIRE AND CHESHIRE ENTOMOLOGICAL Society.—November 17th, 1918.—The President in the chair—Mr. W. Bowater, B.D.S., F.E.S., Brandon Lodge, Russell Road, Moseley, Birming- ham, and Arnold W. Hughes, 33, Lacy Road, Everton, Liverpool, were elected members of the Society.—Dr. P. F. Tinne read a paper entitled ‘Insects concerned in the Pollination of Plants,” in which he dealt very thoroughly with the part played by insects in this important process. Dr, Tinne gave many interesting examples, chiefly drawn from the Hymenoptera and Lepidoptera, as to the methods of the various species; he described the structure of the floral organs of plants which facilitated the operations of the insect principally concerned in the pollination; and also indicated how unwelcome or inefficient visitors were repelled and imprisoned or otherwise prevented from interfering with the process.—The fol- lowing exhibits were made :—By Mr. W. A. Tyerman—A fine bred series of Notodonta dromedarius var. perfusca, Dianthecia nana, D. cucubali, and Phibalapteryx vittata, from the Southport district ; also Sphinx convoluuli, Nemeophila plantaginis, and Callimorpha dominula. A specimen of Cherocampa neri, captured by a farmer near Ainsdale on September 14th, 1913; it was in a very dilapidated condition, but easily recognisable, and it forms a very interesting addition to our county list—Mr. W. Mansbridge showed a short series of Thera variata and pale forms of 7’. obeliscata for com- parison.— Wm. Manssrince, Hon. Sec. - REMEMBER! he. ORIGINAL and LARGEST BUTTERFLY FARM in the BRITISH ISLES is HEAD’S. cai 3 “(Esraprisnep 1884.) Au Immense Stock of Fertile Ova, Living Larva & Pupa, & Set Specimens always on Sale. 3 Many GOOD VARIETIES and HYBRIDS frequently in Stock. Bagels and Cabinets of the best quality supplied. Price List sent free. - Note the Address— ud erly WV. HEAD, Gxiontlnek BURNISTON, “NEAR SCARBOROUGH. 2 we ‘Sehr THE Ae eure AL: SCIENTIFIC CABINET MAKERS. wz T. CROCKETT & SON _ Makers of every Description and Size of Cabirfets, Cases, Store Boxes, Apparatus, and Appliances. _ And Dealers~in all kinds of Specimens for Entomologists, Botanists, Ornithologists, Geologists, Mineralogists, Numismatists, Conchologists, &e., and for the use of Lecturers, Science Teachers, Colleges, Students, “ce. : ‘ ; MUSEUMS FITTED AND ARRANGED. @ Specially made Cabinet for Birds’ Eggs and Skins. The Drawers graduate in’ depth, and are all interchangeable. ALL BEST WORK. ESTIMATES GIVEN. t= All Goods at Store Prices. Great advantages in dealing direct with the Makers. Send for Full Detailed Price List before.ordering elsewhere. 34, RIDING HOUSE STREET, PORTLAND PLACE, W. LEONARD TATCHELL & Co., Breeders and Collectors of British Butterflies and Moths. 23, THE ARCADE, BOURNEMOUTH. Offer their New Lists of LIVING LARVA and PUPS, Imagines, Life-histories, and APPARATUS. MANY GOOD VARS. & MELANIC FORMS. 10, 12, 15, 20, ANnp 40-DrAWER CABINETS FoR SALE. FULL PARTICULARS ON APPLICATION. IY ee es Pe ee re - 2 aT eee = 1 MPROVED LABOUR-SAVING DATA LABELS— as supplied to leading Lepidopterists and Museums. The pecuniary and scientifie value of a collection is enhanced by affixing to every specimen—bred, caught, or received in exchange—a neatly printed data” Jabel. Usual type, one to five localities, equal quantities ; locality, date (= 191 ve - and collector's name (three lines in all)—1000 for 2s. 6d., 3060 for 5s. Unequal ~ numbers, or each additional line, 6d. extra, i FISTS, for pointing out varieties, 6d, per 100, 300 for 1s. 4 Special -—MINUTE LABELS, printed i in the SMALLEST TYPE MADE, essential _ for Micros., and the lesser Macros., or small insects of other orders; spe cimens and Lae on application. - Write for full range of samples before ee your orders for-the season. 4 3 ' $ ee a FRANK LITTLEWOOD, 22, HIGHGATE, KENDAL. | c 0 N ye EB N PS. cer oe A New Spdaibe of Metancea from France (with illustrations), Rovian a 49. A New Species of Chirothrips (Thysanopteya) from South ae ae oo ie 3 illustration), C..B. Williams, 61, A New Species of Eurytoma from Queensland, _ which lives in the stems of Hucalyptus, A. A. Girault, 58. “New: Central - ee American Syntomide, A. #. Gibbs, 54. A Buttertly Hunt in some parts of _ Unexplored France, H. Rowland- Brown (continued), 55. Some es Lepidoptera of La Sainte Baume, V far, S. France, (Rev.) F. E.. ‘Lowe, 60, Notes on the Dragonfly Season of 1913, F'. W. dH. Campion, 63. Forficula — aurieularia (with illustration), H. H. Brindley; 65. ‘The Neuroptera of Nottinghamshire, J. W. Carr, 66. A New Genus of Trydymine eam (Hymenoptera Chalcidoidea), A. A. Girault, 68. NorEs AND OBSERVATIONS, 69. Socierizs, 72. [®- STAUDINGER & BANG- HAAS, Blasewitz- Dresden, i in their son the — new Price List No. LVI. for 1914 (116 pag.), offer more than 20,000 — Species of well-named LEPIDOPTERA, set or in papers, from all parts of the world, in finest condition; 1600 kinds of PREPARED LARVA, &. SePARATE © Price Lists for COLEOPTERA (30,000 species, 208 pag.), for HYMENO- te PTERA (3600 species), DIPTERA (2900), HEMIPTERA (2500), ORTHOPTERA (1200), NEUTERA (630), BIOLOGICAL OBJECTS (800). Dikcca ry Cun . orders. Priceslow. We sell no more living pupe. BRITISH AND EXOTIC LEPIDOPTERA. Tuesday, February 10th, at 1 o’clock. . R. J. C. STEVENS will sell by Auction at his rooms, 88, King Street, Covent Garden, London, W.C., BRITISH LEPIDOPTERA, including about 150 Lots, of varieties of Abraxas grossulariata, reared during the last two seasons by the Rey. G. H. Raynor. They are in very fine condition, and among them are some remarkable flavipalliata, together with other generally unobtainable forms ot very distinct types. The collection formed by the late Mr. B. E. Jupp, of Haslemere, including many bred specimens, Other collections of BRITISH LEPI- DOPTERA, including three nice specimens of C. dispar. Cabinets. EXOTIC LEPIDOPTERA, including some scarce specimens. Catalogues in course of preparation. “DATA” LABELS FOR LEPIDOPTERA. 2/6 per 1000. 1 to 6 sorts, equal numbers, any wording, see specimens below :— H. Smith, W. Davis, A. Langley, F. Roberts, Dare ath Wood. New Forest, Rannoch. 19 19 P zc 19 if unequal numbers are ordered, 6d. extra will be charged. Misimum charge for small quantities, 1/6. These are neatly printed similar to the above. We have supplied these labels to Entomologists i in all parts of Great Britain and abroad. We also supply labels for minute insects printed in the Smallest Type made (see peta ae below). These are 3/6 per 1000, ic Smith W. Davis, eds mnEley, ¥. Roberta, bth bi worl, New Forost. beh Bannpel, J. & W. DAVIS, ce, Museum Works, Dartford, — JAMES GARDNER, MANUFACTURER of ALL KINDS of ENTOMOLOGICAL APPARATUS a 52, HIGH HOLBORN, anp ‘> 9 Ms 29, OXFORD STREET, nearly opposite Tottenham Court Road. £ PRICED LISTS ON APPLICATION. All Articles Guaranteed: exchanged if not approved of. Friends and ‘Customers aN are requested to note the Addresses, as mistakes 0 oceur daily. Sk + Entomologist ’ (6s, post free) for 1914 are now due to: Rest cpewmn an & Co., 34, Hatton Garden, London. et ey ne ae “MARCH, 1914. | me were es IST. eRe al aa “Manly Journal “4 OF ~ GENERAL ENTOMOLOGY. . : “EDITED. BY RICHARD! SOUTH, F.E:S. ir, « RNs Seal) ge boy a TAL Yard ky WITH “THE ASSISTANCE OF ~ : ) Ds “ROBART ADKIN, ¥.0. Si: 0. J, GAHAN, M.A., F.E.8. | -H.ROWLAND-BROWN, M.A.,F.E.S. Ww, J. LUCAS, B.A., F.E.S. | OW. L. DISTANT, V.E.8., &. CLAUDE MORLEY, F.E.S., F.Z.8. : ons ae ees. F. AD: U.| Dr. D. SHARP, F.R.S., F.ELS., &c. i Bs ‘«By mutual confidence a mutual aid wt i ra Oo . / i NE * ye Great. deeds are done and great discoferios made,’ i iY Ma 2 4 eo LONDON: ee ) “WEST, NEWMAN & OO., 54,, HATTON GARDEN i. 'SIMPKIN, MARSHALL, “HAMILTON, KENT & CO., Limrep. WATKINS & DONCASTER Naturalists and Manufacturer of Entomological Apparatus. ‘and Cabinets 3 Plain ser Nets, wire or cane, including | Stick, 1s. 3d., 26., 28, 6a. Folding Nets, 38. 6d., 4s. Umbrella Nets (self-acting), 7 ih. Pocket Boxes, 6d,, 9d., 1s., 18 6d. Zine Relaxing Boxes, 9d., 1s., 18. 6d., 28. Nested Chin Boxes, Wa. per four dozen. Entomological Pins, assorted ‘oviixad, 1s., Is. 6d. per oz. Pocket Lanterns, 28. 6d. to 8s.. Sugaring Tin, with brush, 1s. 6d., 2s. Sngaring Mixture, ready for usé, — 1s. 9d. per tin. Store Boxes, ‘with camphor cells, 28. 6d., 48., 5s., 65. petiyey | Boards, flat or oval, 1 in., 6d.5 1} in., 8d.; 2in., 10d. ; bing 1s.; Bhin., Is. 4ai; 4 in., 1s. 6d.; 5 in., 1s, 104.5 “Complete Set of fourteen Boards, 108. 64. sitting | Houses; 9s. 6d:, 11s. 6d.; corked’ back, 14s. Zine Larva Boxes, 9d., 1s., 1s. 64. Breeding Oage, on 6d., 48., 58., 78. 6d. Ooleopterist’s Collecting Bottle, with tube, — is. 6d., 1s. 8d. Botanical Cases, japanned, double tin, 1s.6d., 28.9d., 8s. 6d., 48. 6d. Rotanival Paper, 1s. 1d., 1s. 4d., 1s. 9d., 28. 2d., per quire. Tnsent Glazed Cases, 2s. 6d. to 11s. Cement for replacing ‘Antennse, 4d. per bottle. Steel Forceps, — 1s, 6d., 2s., 28.6d. per pair. Cabinet Cork, 7 by 84, best quality, 1s.6d. per dozen sheets. Brass Chloroform Bottle, 28. 6d. Insect Lens, 1s. to 8s, Glass-top and — Glass-bottomed Boxes from 1s. per dozen. Zinc Killing Box, 9d., 1s. Pupa. Digger, in leather sheath, Is. 94. Taxidermist’s Companion, containing most — necessary implements for Rae 10s. 64. Scalpels, 1s. 8d.; Scissors, 2s. per — pair; Hgg-drills, 2d., 3d,, ; Blowpipes, 4d., 6d.; Artificial Eyes for Birds and Animals} ; Label-lists of a ae Butterflies, 2d.; ditto of Birds’ Eggs, 2d., 3d., 6d. ; ditto of Land and Fresh-water Shells, 2d. ; Useful Books on Insects, Reps, ke. eg SILVER PINS for collectors of Micro- Lepidoptera, &c., as well as minute insects of all other families. We stock various sizes and lengths of these Silver Pins, which have certain’ advantages over the ordinary pins, whether enamelled, black, or silvered or gilt. For instance, insects liable to become greasy, and verdigrisy like Sesiide, &c., are best pinned on Silver Pins, which will last much longer. We shall be pleased to send patterns on application. SSH OW REQ LONM 3 P20. RYAN Be aps Of every description for INskcrs, Birps’ Kaas, Coins, Microscopical, OpsEcTs Fossiis, &c. Catalogue (100 pp.) sent on appiication, post free. - A LARGE STOCK OF INSEOTS AND BIRDS’. ee (BRITISH, KUROPEAN, AND EXOTIC). mat Birds, Mammals, de., Preserved and Mounted by Firat-claaez Workmen. 86.) STRAND; W.C., LONDON, ENGLAND. Ce aa ROO EE RYE a | T-EW MAN’ S WATER PURIFIER.—A boon to every breeder ; saves endless work and prevents mnch disease in larve. No more stinking water and putrid food in your cages. All ‘know ‘that nettles, dock, and most’ food: -plants, when placed in is of water, become putrid, and the water stinks in a few days. T have discovered a preparation which, placed in the bottom of a jar or any water-receptacle, will keep the water clean and sweet for weeks, and the food-plant from decaying in the water. Price 7d. and Is. 1d. post free. -Sprinc Prick List READY, MANY BARGAINS, WRITE AT ONCE FOR ONE, REMEMBER NEWMAN’S RELAXING TINS. L. W. NEWMAN, F.E.S., BEXLEY, KENT. Dor. otea Andreniformis, 9s.; Tiliz, Ocel- latus, 2s. 6d.; Carpini, 1s. 9d., per doz. Ligustri, Versicolor, dd.; Porcellus, 4d. each. Several 18. x 12 x; 4 in,’ Storeboxes, fitted each side with glazed lifting frames. Cost 10s, 6d., as new,.7s. Lists. © A. FORD, 36, IRVING ROAD, BOURNEMOUTH. The Entomologist, March, 1914. Plate I. 10 Photos G. T. Lyle. Meteorus albiditarsis, female. 2. M. niger, female. M. niger, male. 4. M. fragilis, female. Cocoon of M. melanostictus from which the hyperparasite Mesochorus crassimanus emerged. Cocoon of M. pulchricornis showing the cap remoyed by the imago in emerging. Cocoon of M. albiditarsis. 8. Cocoon of M. ictericus. Cocoons of M. leviventris. 10. Cocoon of M. deceptor. THE ENTOMOLOGIST Vou. XLVII.] MARCH, 1914. [No. 610 CONTRIBUTIONS TO OUR KNOWLEDGE OF THE BRITISH BRACONIDA. No. I. METEORIDA. By G. T Lyte, F.E.S. (PuateE I.) Waritine in 1898, the late George Carter Bignell, to whom we owe, perhaps, more of our knowledge of the British Braconide than to any other, mentions that the number of British students of the Ichneumonide during the nineteenth century would not amount to a dozen. As regards the Braconide, since Bignell published his South Devon list in 1901,* I am not aware of any literature having appeared on the subject in this country, with the exception of a few scattered notes in various periodicals, and Mr. Claude Morley’s papers which were published in the ‘Entomologist’ for 1906, 1907, and 1908. There would seem to be several reasons for this neglect of a most interesting group, one being the want of a cheap text-book on the subject to encourage the young student, and another the fact that several authors have described new species from in- sufficient material, often from a single specimen, so that where species run so closely together and individuals vary so much, a certain amount of confusion has arisen. The Rev. T. A. Marshall, however, did much to dispel this in his excellent monograph, published in the Trans. Ent. Soc. 1885-1889, and even more in his three volumes on the Braconid comprised in ‘Species des Hyménopteéres d’Kurope et d’Algérie,’ 1888-1901. During the past ten. years I have given a good deal of attention to the breeding of hymenopterous parasites, and although the work has been considerable I feel that the results have repaid me, as in no other way could a knowledge of the life- histories of the insects be obtained. I am also much indebted to various gentlemen who have been good enough to present me with specimens which they have bred, often, I fear, much to their disgust, and particularly to Mr. Claude Morley who has * ‘The Ichneumonide of 8. Devon,’ part 2, Braconide, Trans. Devons. for Advan. Sci., Lit. and Art. f ENTOM.—MARCH, 1914. G 74 THE ENTOMOLOGIST. very kindly forwarded to me the whole of his collection of Meteoride for inspection. Ashmead, in his classification of the Ichneumonide,* divides his subfamily Meteorine into five genera, restoring Zemiotus and Protelus (Forster) which had been rejected, apparently for very good reasons, by Marshall. For convenience sake, however, I will treat our British representatives as of but one genus, Meteorus, Hal.,t as did Morley in his notes.t The British species are comparatively few in number, some thirty-five or so having been recorded, including two or three rather doubtful ones. They are distinguished by having three cubital areolets on the fore wings, and, as in the true ichneumons, a petiolated abdomen. While usually parasitic on the larve of Lepidoptera, some are known to prey on the larve of Coleoptera, and Morley has published a record of M. versicolor having been bred from the larva of a Tenthredinid. From April until late autumn they are to be found on the wing, and although I have no knowledge that they ever hibernate in the perfect state, it is possible that at least M. jilator, which has often been taken in November, and M. melanostictus which | have found so late as December 17th, may do so. Most of the Meteoride are solitary parasites, though a few are social; of the former several weave brown shining cocoons which are suspended by a silken thread from leaves or twigs of the plant on which the host has fed. This swing rope is generally from a half to two inches in length, though I have known it to reach eight inches. Marshall writes of these cocoons§: ‘‘ The head of the insect is always turned downwards, and, as it spins by the mouth, we have to account for the fact that somehow it is able to reverse its position in the air, since at the moment of its first suspension the head would naturally be uppermost; so far as I know, no observation has yet been made to explain this circumstance.’ With regard to this, I have several times watched the larva of M. pulchricornis emerge from its host, and the proceeding is somewhat as follows :— The head of the parasite larva is, of course, protruded first, and when about half the body is free a pad of silk is spun on the leaf or twig on which the host rests; after this the remainder of the body is withdrawn, and the parasite lowers itself from the pad by a thread of silk, the head being uppermost, as mentioned by Marshall. By a severe muscular effort, which is not always successful at the first attempt, the apical segment is now brought up until it touches the mouth, and apparently the thread is grasped between the apical and the adjoining segments,|| the * Proc. U. 8. Nat. Mus. vol. xxiii. 1900. + Halliday, Ent. Mag. iii. p. 24. { *Kntomologist,’ 1908, p. 125. § Trans. Ent. Soc. 1887, p. 89. || Berthoumieu describes the pedal processes on the apical segments of larvee of Ichneumonide in Ann. Soe. France, 1895. KNOWLEDGE OF THE BRITISH BRACONIDZE. 75 attachment being at once made secure by the addition of a few twists of silk, after which the head is drawn away leaving the larva suspended by its anal extremity; the formation of the cocoon is then commenced. Some two hours are occupied by the larva in covering itself with the cocoon, but for many hours afterwards it may be seen hard at work spinning within. In all the cases observed by me the parasite larva emerged from the side of the seventh or eighth segment of the host, I believe, through a spiracle. As I mentioned before, I know of no instance of a Meteorid hibernating in the perfect state, but with several species the winter is passed within the body of the host, either as an ovum or young larva, and with a few others as a larva within the cocoon. My experience is that pupation does not take place until within a fortnight or so of the emergence of the imago, no matter how long a period may be spent within the cocoon. On emerging, the imago removes a neat cap from one end of its cocoon (fig. 6) ; with those species which construct fusiform cocoons the cap is always removed from the smaller end. In the following notes, unless otherwise stated, the records are my own, and the insects mentioned have been captured or bred in the New Forest. Meteorus albiditarsis (Curtis).* (Fig. 1.)—This, the largest species we have, may easily be distinguished from all other British Meteoride by having the radial areolet of the under wing divided by a distinct transverse nervure. It seems to be generally distributed and is fairly common in May and June; on those dull cold days which are, as a rule, only too frequent in the late spring, it may often be beaten from thorn bushes. A solitary parasite of the larvee of Noctue, the parasite larva emerging from the host when the latter is about to pupate in its subterranean earthern cocoon, within which the cocoon of the parasite is constructed. Marshall well describes this cocoon as ‘‘felted stramineous with some loose flocculence’’; it consists of three layers, outside the ‘‘ loose flocculence,” which easily comes away when the cocoon is handled, then the cocoon proper, which is rather similar in colour'and texture to that of the ‘‘silk worm”’ of commerce, and within this a thin transparent, brownish envelope of a material much resembling goldbeater’s skin. On October 1st, 1913, I exhibited at a meeting of the Entomological Society of London a skein of silk wound from two of these cocoons (fig. 7). At least a period of ten months appears to be spent in the larva state, in which condition the winter is passed within the cocoon. I believe that sometimes even a second winter is so * ‘British Entomology,’ pl. cecexv. G 2 76 THE ENTOMOLOGIST. passed, for a cocoon which was spun in June, 1912, was found to still contain the larva, living and unchanged, in September, 1913. The female somewhat resembles Zele testaceator (Curtis), with which species it has frequently been confused in collections; in Zele, however, the recurrent nervure is very widely rejected, and the abdomen does not possess a true petiole, as in Meteorus. I have bred it from a cocoon dug up at roots of an oak tree, April 14th, 1904, from larva of T’eniocampa miniosa, May 11th, 1918, and also from larve of T. gracilis, T. pulverulenta, T’. stabilis, and Panolis piniperda. M. chrysopthalmus (Nees).*—I possess 2 male, beaten from birch, May 5th, 1912, which I must refer to this species, as the costal cell is slightly longer than the median. Very similar to the next, though the females differ in the length of the terebra. M. deceptor (Wesm.).t— Generally bred from larve of Geometre, a solitary parasite. The cocoon is white, felted, fusiform and without loose flocculence; it is found within that of its host, which is usually underground, 9} mm. in length (fig. 10). I have obtained this parasite from larve of Gonodontis bidentata and Semiothisa liturata in May. Single brooded, the winter being passed in the larva state within the cocoon. In Morley’s collection is a pair bred by Clutten at Burnley, from larve of a geometer; in this case the male is testaceous and not nigropiceous. M. ictericus (Nees).—Marshall considered this to be ‘‘ perhaps the commonest British species.’ Although fairly plentiful, there are certainly others that are far more so, at any rate, in the New Forest. It would seem that Curtis, Halliday, and other writers con- fused this species with M. pulchricornis, and even Marshall cannot have seen the cocoon, for he assumes Curtis’s figure to be correct, and describes it as “‘ pensile, yellowish brown, shining, and semi-transparent.” Bignell, however, is correct in saying that it is ‘‘white and very thin,” and so early as 1884 Bouché t described the cocoon as ‘albus chartaceus’’ and not -pensile. All that I have seen agree with the descriptions of Bignell and Bouché, being cylindrical, not fusiform, and constructed within rolled leaves. The transformations of the insect are visible through the cocoon (fig. 8). Generally bred from larve of Tortrices, a solitary parasite. I have obtained it from a cocoon found on oak, June 6th, 1910 (New Forest), and also from larve of either Sericoris fabricana or S. lacunana taken at Burgess Hill, Sussex, May, 1911. In Morley’s collection is a female bred by R. Adkin, October 12th, 1910, from a larva of T'ortrix pronubana, and two males bred by * Nees-ab-Esenbech. Hym. Ich. Affinium Mon. vol. i. 1834. + Wesmael, Nouv. Mém. Ac. Brux. 1835. } Naturgesch. d. Ins. The Entomologist, March, 1914. Plate II. W. J. Lucas del. SYMPETRUM STRIOLATUM. NymMPH (x about 4). BRITISH ODONATA IN 1913. 77 R. South from larve of Peronea hastiana, October 18th, 1904, and October 21st, 1904, host from St. Anne’s, Lancashire. M. vexator (Hal.).—Is easily known by the size of the stigma, which is as large or even larger than the first cubital cell, with a considerable pale spot at the inner angle. We are indebted to Morley for redescribing this species,* from speci- mens bred by Keys at Plymouth out of a fungus, together with the clavicorn beetle Diphyllus lunatus (Fab.). Halliday described the female from a single insect, while Marshall, who described its supposititious male, had only a dilapidated specimen before him. In Morley’s insects the antenne of the male are 26-jointed, of the female 24, and the recurrent nervure is rejected. M., atrator (Curtis).—In August, 1913, C. W. Colthrup sent me from Eastbourne two females which he had captured with three specimens of the hyperparasite Hemiteles areator. The insects were caught while running about on furniture which was infested with the moth Tinea biselliella, and were evidently searching for the larve of the lepidopteron. Morley has a female which was also taken indoors. I believe that no specified host has before been cited for this species, and it appears to have been but rarely observed, which seems strange in the case of so beneficial an insect. (To be continued.) BRITS ODONATA IN, i19t3: By W. J. Lucas, B.A., F.E.S. (PuateE II.) AutHoueH the spring was an early one, I did not meet with a dragonfly till May 18th, when Pyrrhosoma nymphula and Tibellula quadrimaculata, the latter in teneral condition, were taken at the Black Pond, near Oxshott, in Surrey; no other species was seen—not even Hnallagma cyathigerum. On May 25th the same locality was again visited, when a male and a female of Cordulia enea were taken, and E. cyathigerum was on the wing, as well as P. nymphula and L. quadrimaculata; but, on the whole, dragonflies were not very evident in a locality where they are usually so plentiful by this date. On June Ist a visit was paid to Frensham Ponds and the swampy ground near them, in the south-west corner of Surrey ; but the weather was dull. However, H. cyathigerum was found to be numerous. There were also a few J. elegans, and a female Agrion puella was taken. One or two teneral examples of * Entom. p. 4, 1912. 78 THE ENTOMOLOGIST. Orthetrum cancellatum were met with at the larger pond, and a nymph-skin was secured. Calopteryx virgo occurred in a wet field near the smaller pond, most of the females taken being very dark. On June 8th, another dull day, the canal-side at Byfleet was visited. Owing to the weather, no doubt, dragonflies were not numerous, but A. puella, P. nymphula, and Hrythromma naias were captured. During the first half of June Col. J. W. Yerbury captured for me a few dragonflies in the north of Scotland. They were— Leucorrhinia dubia, a male, June 8rd, at Nethy Bridge; P. nymphula, a female, June 4th, at Aviemore, grasping its prey, a caddis-fly named Limnophilus centralis; EH. cyathigerum, three males and a female, at Aviemore, from June 6th—16th, the male taken on the 16th holding its prey, a small moth named Crambus pratellus; Agrion hastulatum, nine males and two females, at Aviemore, from June 9th-16th. The last-named species varied much in the development of the lateral marks on the second segment of the abdomen, and from two they were nearly or quite absent. Females of this species seem seldom to be captured. On June 21st Mr. P. Richards found J. elegans in swarms at Seabrook, in Kent, and sent me a male for identifica- tion. On July 29th Col. Yerbury obtained a male P. nymphula at Mynnyd Eppint, in Wales, at an altitude of about 1500 ft. ; no other dragonfly was seen. In the New Forest, from June 27th—29th, dragonflies were found to be fairly numerous. A. puella, Platyenemis pennipes, P. nymphula, and Orthetrum cerulescens were common, but the last species was in teneral condition. Calopteryx virgo was out in fair numbers, and there were a few I. elegans, one being obtained of the var. rufescens. Of Pyrrhosoma tenellum one female was taken, but of Cordulegaster annulatus 1 am not certain that I saw a single specimen, although, judging by other records, it should have been on the wing by this date. Neither Agrion mercuriale nor Ischnura pumilio, nor Gomphus vulgatis- simus was met with, although a special search was made for the last two. A week later, July 4th-6th, again the same two species were not to be seen; but A. mercuriale was taken plentifully behind Holm Hill, one only, however, being a female, which was found to be attacked by red acari. On this occasion P. tenellum was met with again. From July 27th onwards some time was spent in the New Forest, and on July 28th a visit was paid to the pond on Beau- lieu Heath, where Sympetrum fonscolombii was taken in 1911. Though I sought for over an hour in the bright, hot sunshine, the only dragonflies found were Lestes sponsa, P. tenellum (and its var. melanotum), I. elegans, E. cyathigerum, O. caerulescens, a Libellula depressa and an Anax imperator somewhat doubtfully, and Sympetrum striolatum. I feel certain that amongst the last BRITISH ODONATA IN 1918. 79 was not a single S. fonscolombii, though offspring of the 1911 specimens, if they had bred there, would probably have been due in 1918. Mr. F. H. Haines, of Winfrith, Dorset, was a little more successful with this species. Writing August 8rd, 1913, he told me that on July 24th he saw several specimens on a pond at Morden and took a male and female in cop.; as well as a second male. They were in nothing like the abundance of 1912, and their wariness was wonderful. He might have made twenty captures of S. striolatum for one of S.fonscolombii. On July 25th he tried West Knighton pond and thinks he saw one of the latter species, but could not capture it. A friend of his having reported the species at Creech, south of Wareham, on August 2nd they together visited both Creech and Morden, but found nothing, though S. striolatum was abundant at Creech, and they took an Avschnia juncea and a worn A. imperator at Morden. Mr. Haines did not find the pond at Creech such a one as he would associate with S. fonscolombu, although his friend knew the dragonfly. It prefers heathland ponds, fed by swamps with much decomposing vegetable matter in them all round, causing the water to be very warm. The Creech pond was deep and cold. He thought perhaps a swarm might have paid a visit and passed on. Some days previously he found the species still well in evidence at Morden and took another male. So this year he has four specimens, three males and one female— three taken on one day, one on another. On August 1st C. annulatus was common at Beaulieu River, and from this time there appeared to be no dearth of them in the Forest, so the adverse season of 1912 had not affected the 1913 imagines. On the same date an Avschna cyanea, female, was captured, apparently but recently emerged, as the spots were whitish-blue. On the next day an 4. juncea was captured at Woodfidley. On August 16th in the central part of the Forest dragonflies were numerous, almost all being S. striolatum. On August 25th I could not find A. mercuriale, and presume it was over. J. pumilio I was not able to find at all during the season. Towards the end of August C. virgo had disappeared. Mr. W. H. Harwood tells me that a specimen of schna isosceles was taken at Wicken Fen on September 28th, which seems to be a very late date for this species. After a long absence, a visit was paid to the Black Pond on September 28th, when S. striolatum and S. scoticum were found to be plentiful. There were also a few Aischnas, of which males of 4. juncea and AL. grandis were captured; the former settled on the front of my coat and was there netted. Judging by size Af. mata appeared to be present also. Mr. K. J. Morton is able to record that a female Hemianax ephippiger was found in Ireland (vide E. M. M. Jan. 1914) in October, 1913. This is, of course, an accidental occurrence, as 80 THE ENTOMOLOGIST. was that of the female of the same species which was taken flying in a street in Devonport on February 24th, 1903.* On November 16th the Black Pond was again visited to see if S. striolatum was still on the wing. The latest date on which I had previously seen it was November 14th in 1897, and as the autumn was mild there was a chance of a later date being recorded. None were seen, however; but it is quite possible that they were not over, for the weather was not altogether favourable. Some very interesting notes have come to hand concerning this, which is perhaps the commonest of English dragonflies. Miss D. Molesworth, of Brighton (in litt., Oct. 21st, and again Noy. 6th, 19138), told me that she had had under inspection a number of S. striolatum from the deposition of the egg till the emergence of the imago, the whole life-cycle occupying less than a year. The female was caught ovipositing on September 18th, 1912, and, after being kept from water, was on September 20th held over it, when she gave more eggs. These hatched between October 21st and 25th. The nymphs did not grow at a uniform rate, and the wing-cases appeared on the largest towards the end of April, 1918. By June, four of the nymphs had reached a length of 16 mm. and then became restless. There were plenty of water-weeds in the aquarium, but they did not attempt to climb, though earlier in the year many ‘‘demoiselles”’ had scaled the water-plantain leaves and successfully emerged. Miss Molesworth then had to leave them for three weeks and on her return all four were dead. Meanwhile, others had reached the same stage; but as each attained a length of 16 mm. it died. In August a bank was made in one corner of the aquarium, reaching above water-level, and strips of wood about two feet long were inserted in it. In September the nymphs began one by one to climb to various heights—some to the top, some less than six inches. The first emerged on September 4th and the last on October 12th, 1918. Before the last had emerged, the boards were removed and a bank was built round the water-plantain stems. The nymph climbed and the imago emerged quite happily. That the earlier ones were ready to emerge was clear, for they partially did so under water. The female, from which the eggs were obtained, was depositing them in water not more than six inches deep, and the nymphs were kept in water ° of about that depth. In water of greater depth they left the bottom and began to crawl on the weeds. In 1913 another female deposited eges on August 26th, and the first nymphs: emerged on September 14th, less than three weeks later, but they were kept in a warm room! The largest nymph was 4mm. long on October 21st; it was observed demolishing a smaller companion. * Figured, natural size, in ‘ Entomologist,’ xxxvii. pl. 3. BRITISH ODONATA IN 1913. 81 It should be stated that the aquarium in which the 1912 nymphs wére bred was standing on a brick window-sill, where the window was open day and night all through the winter. The weather being mild the water did not freeze, though it did in former years. In fact a nymph of a larger species was on one occasion frozen in the middle of a solid piece of ice and remained so for two days. When the thaw came it revived and seemed none the worse. These nymphs were not forced, there- fore, by unusual heat, but probably were by receiving an unnatural amount of food. As soon as they began to eat Chironomus larve, they were fed almost daily and when nearly full-grown would sometimes eat as many as eight in succession, though each was as long as the nymph itself. Probably in confinement space has something to do with the rate of growth. For a few kept in a very small bottle with abundance of food scarcely grew at all, and when they were moved into a larger aquarium, where food must have been more difficult to procure, because less plentiful, they were found to be scarcely more than half the size of some which had already been there for six weeks. All emerged in the early morning, usually on dull days. One nymph showed a particular aversion to sunshine. Being ready to emerge, it crawled out of the water ona cloudy morning. When on the wood the sun came out rather suddenly, and the nymph immediately scrambled and fell down. As soon as the sun disappeared it climbed up again; but on the sun’s reappear- ance it repeated its previous performance. It did this three times, and the nymph was not contented till the aquarium was shaded, when it emerged none the worse for what had happened. Miss Molesworth’s interesting notes may suitably be supple- mented by a description* and figure (Plate II.) of a full-grown nymph of S. striolatum, which I have therefore prepared :— Description.—General colowr sepia, from very pale to quite dark. Length, including anal appendages, about 18 mm.; greatest breadth, about 7mm. Head of moderate size; in outline a flattened pentagon ; width about 5°56 mm. Antenne of seven segments, the basal two short and rather swollen, the rest more slender, with a ringed appear- ance. Mask (labium) tapering backwards to the middle hinge where it is narrow; this hinge’ almost as far back as the insertion of the midlegs; extremity spoon-shaped, covering the face; palpi broad, where they approach one another and there serrated ; teeth reddish ; movable hooks, long, sharp, slender; centre of Sabium produced in an obtuse angle; on this lobe, internally, are two semicircles of long reddish hairs, about fourteen in each, the lateral margin of each palpus fringed with a similar row of hairs, pointing inwards. Several pale marks in front of vertex, which also has pale markings. Hyes * A figure of S. vulgatum (= striolatwm) in W. H. Nunny’s paper, ‘Science Gossip,’ July, 1894, does not appear to represent a Sympetrum at all, and is certainly not S. striolatum. 82 THE ENTOMOLOGIST. prominent, somewhat hemispherical, situated at the fore-corners of the head. Occiput rather broad, rough, bearing some long hairs. Top of head as a whole slightly convex. Prothorax collar-like, a dark patch in centre, hind-margin convex. Mesothoracic spiracles dark, very conspicuous. Meso- and metanotwm variegated with lighter and darker tints. Legs long, slender, joints darker; femora and fore- and mid-tibiz ringed with darker sepia bands; fore- and mid-tibize hairy, hind tibia rather spiny; fore-legs about 10 mm. long, mid-legs about 11 mm., hind-legs nearly 16 mm. Wing-cases about 5 mm. long. Abdomen broad and somewhat flattened; with pale, long, slender, recurved mid-dorsal spines on segments six, seven and eight, and a small one on five hidden by the wing-cases; a pair of lateral spines on eight and nine, those on eight being of moderate length, those on nine conspicuously long, equal in length to the last two segments; two or four dark dots on the dorsal part of several of the hinder segments; also lines of paler or darker suffusions on the dorsal surface, which vary considerably according to the depth of colouring of the specimens; ventral surface of nymph-skin fairly uniform in colouring. Anal appendages short, hairy; wpper, tri- angular, pointed; laterals, shorter and more slender; lower, more than half as long again as upper, and flat when looked at from the side. It is somewhat difficult to describe the hairiness of a dried nymph-skin, consequently it has been little referred to. [Material.—(i.) A nymph-skin from which a male imago emerged on July 28th, 1903; (i1.) askin of a nymph, taken in Richmond Park, Surrey, from which a male was bred on July 10th, 1903; (iii.) other nymph-skins found under such conditions as to admit no doubt of their identity. Nos. i. and ii. were the specimens chiefly employed. The figure is enlarged a little over four times. ] THE EARLIER STAGES OF COLIAS HECLA. By W. G. SHeupon, F.E.S. So far as I am aware, the only lepidopterist who has written anything on the earlier stages of this beautiful Arctic species is Staudinger, and his brief note is in one important respect inaccurate. Staudinger, who passed the summer of 1860 in the north of Norway, during his sojourn there met with Colias hecla abun- dantly, near Bossekop, in the Alten Fjord. He states: ‘‘the headquarters of this species was a flat sandy peninsula in the bed of the River Alten”; in this place ‘“‘ Phaca lapponica, De Candolle, the undoubted food-plant, grew very abundantly, and I noticed the females ova-depositing thereon.” The Phaca lapponica of De Candolle is, according to the ‘Conspectus Flore Kurope’ of Nyman, now known as Ozytropis lapponica, a plant which, so far as I know, does not occur at Bossekop ; at any rate, I carefully examined the headquarters of THE EARLIER STAGES OF COLIAS HECLA. 83 C. hecla described by Staudinger, during my stay there in 1912, and the only leguminous plant I could find in the district was the Astragalus alpinus of Linné, which the ‘ Index Kewensis ’ states is the Phaca astragalina of De Candolle, and which grew freely, locally. Later on, at Laxelv, in the Porsanger Fjord, as noted in ‘Entomologist,’ xlv. p. 339, I found C. hecla in great numbers, flying over flat rough meadows and fields in which A. alpinus grew abundantly ; this plant is undoubtedly its food-plant there, and almost certainly, for the above reasons, at Bossekop also. I do not, of course, know in how many localities in Lapland —a great part of which is entirely unexplored—C. hecla is found, and if it is always associated with A. alpinus, but it is certainly a very local species, found only in the above-mentioned localities of those I have explored, although it is stated to occur also on the north side of the Tornea Traske in Swedish Lapland. In all of these localities A. alpinus is an abundant plant; but it is so local that I do not recollect ever seeing a specimen elsewhere, though I have explored a great many miles of suitable country in Arctic Scandinavia. The only other leguminous plant I could find in the Por- sanger Fjord was what I think was a species of Vicia, which in the latter part of July had beautiful trusses of mauve flowers, and which grew about one foot high, and was plentiful along the shores of the Fjord at Kistrand. This plant the larve of C. hecla refused to feed upon. They also refused white and red clover, which I offered to them on my journey home, and which grew freely at Tromso and at various places touched at south of that town. It seems probable that the larve of the two exclusively Arctic species of Colias occurring in Kurope—C. hecla and C. werdandi —feed exclusively in nature on A. alpinus. It should, however, be noted that C. hecla does not occur on the south side of the Tornea Traske, where A. alpinus is an abundant plant, and where C. werdandi flies in great numbers. The ova of C. hecla were to be found plentifully at Laxelv at the time of my visit, July 11th to July 16th, 1912, almost every individual food-plant éxamined having some attached to it; they are deposited singly. The ova is of the usual Colias type, upright, the vertical and horizontal diameters are 1°25 mm. and 0°65 mm. respec- tively. It has vertical ribs, about twenty-six in number; the distance they are apart is ‘(05 mm.; numerous very shallow transverse ribs connect the vertical ribs. The diameter of the apex of the ovais‘15 mm. The micropylar area consists of a number of shallow cells; it is not noticeably depressed. The surface of the ova is shining and opalescent. The larva emerges from the side. 84 THE ENTOMOLOGIST. The ova from which the foregoing description was made was deposited by a captive female on a plant of A. alpinus, on July 12th; it was then creamy white in colour; on the 18th it had changed to light red, and on the 14th to bright coral-red ; on the 20th it was leaden coloured. The larva emerged on the 22nd. It thus appears that the period of the ova stage is ten days. It will be seen, on reference to my description of the ova of Colias werdandi in ‘ Entomologist’ xliv. p. 122, that the ova of these two species are identical in size and in all other respects, except that in C. werdandi the colour changes to deep orange instead of to coral-red, which the ova of C. hecla does. The period of this stage is in the case of C. werdandi two days longer. Immediately after emergence the larva was 1°50 mm. long. The head was black, the remainder of the segments were dull green, transparent and thickly studded with tubercles, each tubercle having in its centre a spine. The larva at this stage eats holes in the upper cuticle of a leaflet of its food-plant, and rests stretched out at full length on the midrib thereof; it changed into the second stage on July 27th, and was then 2mm. long and stout in proportion to its length. Colour dull green, very spiny, head greenish brown, spiny and shining, the re- mainder of the segments had a dark medio-dorsal stripe, lighter subdorsal area bounded below by darker stripes. The spiracular stripes are lighter than the remainder of the surface of the larva. The change to the third stage took place on August “22nd. The larva was then 4 mm. long; head light amber-coloured ; dorsal area dull dark green; subdorsal areas light green of the same tint, bordered on the lower edges with dark stripes of the same tint as the dorsal area. The spiracular stripes were of lighter green, the ventral area was of the same tint as the sub- dorsal. All the segments were thickly covered with black tubercles, each one of which emitted a black spine. ‘The spiracles were light green with black circumferences. On August 29th the larva was slowly feeding; on September 6th it ceased feeding altogether, and was placed in a cool cellar in a flower-pot which contained dry sand and Sphagnum. My stock of ova when I left Laxelv on July 16th was twenty- two, but by the time I reached England, on August 38rd, they had been reduced to half a dozen more or less unhealthy larve. A. alpinus is a most difficult plant to transplant or to keep fresh and healthy when it is dug up, and all my plants were yellow and unhealthy on arrival at home. Of these half dozen larve only two reached the hibernating stage, and one of these two died soon after being placed in winter quarters, reducing my stock early in October to a single specimen. This larva remained quiescent and stretched out on the Sphagnum. I had intended, upon the first sign of frost appearing, to THE EARLIER STAGES OF COLIAS HECLA. 85 take it out of doors, so that it might get some approach to its natural home conditions in winter, and afterwards to force it, but the winter turned out to be exceptionally mild, and by January 23th, there not having been any frost, I brought the larva up and placed itin a warm room. I didnot have a plant of A. alpinus in leaf, and so offered the larva young leaves of Colutea arborescens, which I had ascertained the previous summer it would eat. On January 22nd it commenced to feed upon these, and fed very slowly for several weeks, so slowly, however, that its daily meal, which was usually taken when the sun was shining, did not exceed a notch in a leaflet the size of an average pin’s head. In the beginning of March it sickened and died. During the time it was feeding in the winter the size only in- creased a very little, not more than a millimeter in length. In all probability, to successfully rear this larva would entail its being kept at a temperature below freezing point for several months. In its natural habitat the snow would probably be gone by the middle of May. Staudinger mentions that at Bossekop the first male was taken on June 18th, 1860, but it certainly was not out there on the day I left, June 22nd, 1912. On my arrival at Laxely on July 11th, fully one-third of the specimens flying about were more or less worn. The season was rather a late one, and I should say that June 20th, as the first date of emer- gence on an average season, is probably not far wrong. Astragalus alpinus in Lapland entirely loses all trace of foliage in the winter, and until the middle of June, or rather later, it does not develop sufficient new leaves to feed the larva upon; this being the case, there seem to be three possible theories of its behaviour after hibernation :— (1) That it has an alternative food-plant. Ido not think this probable for, as before stated, I could not find another leguminous plant in its haunts, and one cannot imagine it feeding upon anything else. (2) That it feeds upon the roots of A. alpinus. This is pos- sible, for this plant has long succulent roots, very much after the style of Lotus corniculatus. (3) That it feeds very slowly through the summer on the leaves of A. alpinus, hibernating a second time, either as a full- fed larva or as a pupa. Iam inclined to think that this latter theory will prove the correct one. The larva I had in confine- ment seemed perfectly healthy and satisfied with its daily minute meal for weeks, which is just what one would expect it to do in a state of nature if this theory be correct, for the leaves until the middle of June are very minute and would not suflice to satisfy a more vigorous appetite. But, of course, my larva had not been subjected to its natural low winter temperature for many months, and one does not know what effect the unusual treatment received might have had upon its appetite. Youlgreave, South Croydon: January 13th, 1914. 86 THE ENTOMOLOGIST. DIADIPLOSIS COCCIDIVORA, N. sp. By E. Porter FE.t. Tue small midges described below were reared in some numbers from a species of Pseudococcus by A. Rutherford, Government Entomologist of the Department of Agriculture, Peradeniya, Ceylon, and forwarded for identification under the date of November 27th, 1913. This species appears to be congeneric with D. cocci, Felt, a species reared earlier by Mr. William H. Patterson from larve preying upon the eggs of black scale, Saissetia nigra, in St. Vincent, West Indies. The two species are quite different, and further studies may result in their being referred to different genera. g. Length 1 mm. Antenne probably half longer than the body, presumably thickly haired, fuscous yellowish ; fourteen segments, the fifth binodose, the two portions of the stem each with a length approximately a quarter greater than the diameter, the distal enlarge- ment with a length a quarter greater than its diameter, and bearing two moderately stout circumfili. Palpi: the first segment small, globose; the second with a length nearly three times its diameter ; the third a little longer, more slender. Mesonotum dark yellowish brown, the submedian lines, scutellum and postscutellum fuscous yellowish. Abdomen fuscous yellowish. Wings hyaline, the third vein uniting with costa at the apex of the wing, the fifth joining the posterior margin at the distal fourth, its branch at the basal third. Halteres and legs a nearly uniform fuscous yellowish, tarsi probably somewhat darker; claws moderately stout, strongly curved, the anterior and mid unidentate, the posterior simple, the pulvilli about half the length of the claws. Genitalia: basal clasp segment moderately short, stout ; terminal clasp segment short, stout, with a rather large, strongly curved apical spur; dorsal plate long, deeply and triangularly emarginate, the lobes narrowly rounded and sparsely setose ; ventral plate moderately long, tapering to a narrowly rounded setose apex. Harpes foliate, tapering to a narrowly rounded apex, laterally with a thick patch of long, stout sete; style long, slender, slightly curved. @. Length 15mm. Antenne probably nearly as long as the body, sparsely haired, dark brown ; fourteen subsessile segments, the fifth with a stem one-sixth the length of the cylindric basal enlarge- ment, which latter has a length about thrice its diameter. Palpi: the first segment subglobose, the second with a length more than three times its diameter, the third half longer than the second, and more slender. Mesonotum dark yellowish brown. Abdomen yellowish orange. Ovipositor short, the terminal lobes narrowly oval and sparsely setose, otherwise nearly as in the male. Type Cecid a2486. State Museum, Albany, N.Y. 87 DESCRIPTION OF A NEW CICADA FROM WEST AFRICA. By W. L. Distant. Musoda gigantea, sp. nov. 3g. Head and pronotum pale testaceous, the latter with the fissures darker, and the lateral and posterior margins ochraceous; eyes greyish-white; mesonotum dark ochraceous with darker mott- lings and four obconical spots at anterior margin, the two central spots largest ; abdomen castaneous, the posterior segmental margins, a narrow central longitudinal fascia, and the anal area more or less pale ochraceous ; body beneath pale ochraceous, the face and legs darker and more pale testaceous; tegmina and wings hyaline, venation, costal membrane to tegmina, and narrow basal suffusion to wings pale testaceous; head with the front conically prominent, anteriorly more darkly transversely striate; vertex narrowly longitu- dinally incised between the ocelli; face short, broad and convex, a short, broad, central sulecation on its anterior area, its lateral areas strongly transversely striate; rostrum reaching the intermediate coxe ; opercula not passing base of abdomen, obliquely directed inwardly, their apices rounded and widely separated; anterior femora shortly and finely toothed beneath on apical areas; pronotum some- what broadly, centrally, longitudinally suleate, the fissures profound; abdomen broad, robust, above strongly, centrally ridged, the lateral areas oblique, basal segment strongly, centrally, conically produced, beneath obliquely depressed towards apex. Long. excl. tegm. 3, 29 millim. Exp. tegm. 88 millim. Hab. West Africa; Cameroons (Conradt). British Museum. This is the second but larger species of the genus yet described. A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. By H. Rownanp-Brown, M.A., F.E.S. (Continued from p. 60.) (vi) Basses-Alpes. (b) Larche. To speak of Larche as “‘ unexplored” is less inappropriate, per- haps, than would appear in view of the recorded visits made in past years by French entomologists. Donzel, in the “ forties,” collected hereabouts; but he seems not to have published the results of his expedition as minutely as he has recorded the lepidopterous fauna of Digne and the lower Basses-Alpes. It is to Antoine Guillemot, to Bellier de la Chavignerie, and to Berce that we owe the first detailed accounts of the numerous Lepi- doptera met with at this point of the Italian frontier; and after 88 THE ENTOMOLOGIST. the lapse of fifty-eight years it may be agreeable to those interested in the butterflies of a little-known corner of the Alps to retrace the footsteps of these pioneers. The published account of their experiences given by Guillemot is rare. It is tobe found neither in the library of the Natural History Museum, South Kensington, nor of the Entomological Society of London; and it is only within the last month, and after this paper was printed, that I saw a copy included among the separata of a foreign bookseller. I am indebted, therefore, to the kindness of M. Charles Oberthiir for a loan of the work.* As far as I can see, Larche has changed little in appearance since Guillemot and Bellier were there in 1855, from Jnly 29th to August 3rd. The hotel accommodation is decidedly worse, for while they speak of comfortable quarters and good plain food, 1 am afraid I cannot endorse their recommendation of the inn I visited. However, I was lucky enough to find my bedroom occupied when I came up from Barcelonnette on the morning of the 25th, and by the courtesy and kindness of the Commandant of the garrison, whom I chanced to meet in the road, I was enabled to obtain excellent quarters with M. Mathieu, the local butcher—quarters usually filled by officers of the Alpine regiments on the march and on manceuvres. Both Monsieur and Madame were extremely kind and attentive, and I cordially advise any of my readers who may fancy a week or two at Larche to do as I did—put up in their chalet, lay in a good supply of tinned foods, biscuits, &c., for lunch in the open, and which are for sale at the small grocer’s shop in the village ; and after the premier déjeuner of coffee and rolls, return to the auberge only to dine. In one respect, it is true, Larche has changed. Many of the enterprising inhabitants having amassed fortunes, especially in Mexico, have come back to build large stucco villas and live in their native place, for the summer months at any rate. It is possible, therefore, that with the steady increase of motor traftic into Italy by this route, one of these proud proprietors may devise a scheme for the reception of boarders, though the summer at this altitude—5568 ft.—is short: eight weeks at the most. I did not know, when I decided to finish my entomological tour at Larche, that M. Oberthur’s two collectors from Digne had passed the previous season (1912) there. Nor had I the report of their experiences to guide me, as partly recorded in recent published fascicules of ‘ Lépidoptérologie Comparée’ (Rennes, 1918, fase. vii., ‘Observations sur les Syrichthus du * © Vinet-Cing Jours de Chasses aux Lépidoptéres 4 Barcelonnette, et a Larche,’ par A. Guillemot. Clermont. 1856. Cp., also, ‘Observations sur les Lépidoptéres des Basses-Alpes,’ par Bellier de la Chavignerie, Ann. Soc. Ent. France, 1854, p. 29, 1856, p. 5, and 1859, p. 177. A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 89 groupe d’Alveus’). Also, I had no intention when I left England of visiting the Basses-Alpes at all, but had planned to turn west from Le Vercors (vide antea, p. 8) into Ardéche. I had not provided myself, therefore, with Bellier’s notes, which might have assisted me to the right localities, though a chance meet- ing at Barcelonnette with Mr. E. A. Tucker and Mr. Charles Morris, of Cannes—both ardent lepidopterists—gave me the clue to a locality in which, as I subsequently discovered, these French naturalists made their most important captures. The journey from Barcelonnette is advertised in summer to be performed by motor omnibus. As a matter of fact, when the motor reached Condamine—the half-way house—the driver was seized with a sudden spasm of economy for petrol; and another and altogether ‘‘ ancient piece’”’ was trundled out of the coach- house to perform the last long uphill climb. After the dizzy ordeal of the day before on the Col d’Allos the change was delightful; and as we jogged peacefully along the road it was possible to survey the splendid scenery and to note chance insects on the wayside flowers. But for the greater part of the journey, the forest gradually disappearing and the flora of the valley giving place to the veritable mountain kind, there was little on the wing, as the sun was still hidden behind the ever- rising barrier of the hills. When the room difficulty had been settled, I set off for the Lauzanier valley, the road diverging from that to Italy, and crossing by pastures to the left bank of the Ubayette. The first butterfly to attract attention was a remarkably fine brood of I. lathonia, just emerged and in perfect condition, with males of Epinephele lycaon flitting mera-like over and about the stone walls of the cornfields. On past the bridge, females of A. damon were in some profusion, with P. argyrognomon, C. virgauree— all males—some worn C. hippothoé, var. eurybia females, and a fair sprinkling of Argynnids—aglaia, and niobe, var. eris (very rarely typical). The season was, however, getting late for the mountain meadows; and I quite agree with Bellier, who recom- mends a visit to Larche before they are cut, as with the hay goes much of the best collecting. Down by the stream I could see some small Parnasside swinging lazily over the Sedum beds; and these subsequently proved to be Parnassius delius, rather worn. The steep grassy banks on the left-hand side of the mule path were full of butterflies, chiefly of the commoner alpine sorts; conspicuous by their numbers and exquisite condition being Cenonympha iphis, while occasional Black-and-White Skippers on the track itself were either Hesperia carthami, H. alveus, or Pyrgus sao. Unfortunately, upon the whole length of the green valley, which ends with a steep climb to the Refuge hut, vast herds of sheep, goats, and horses had been grazing ; and it was ENTOM.—MARCH, 1914. H 90 THE ENTOMOLOGIST. here also that for half an hour I sat and watched the strapping Chasseurs Alpins of the French Army defile before me—fresh, merry, and brisk as are all these mountain infantrymen, even with eight hours’ march behind them over these stark moun- tains. The little herbage left by the shepherds’ flocks the army mules seemed to have finished up; and for quite an hour’s walking I encountered practically nothing of note—a few scattered Colias phicomone, a very occasional Hrebia epiphron, var. cas- siope, and rarer Polyommatus pheretes; even Plebeius argus, the ubiquitous, had diminished, and, of course, as soon as I attained a ‘not bad eminence,’”’ in went the sun, down came the mist, and collecting butterflies in the Lauzanier was over for the day, though it was barely one o’clock. So after lunch and a welcome foot-washing in the torrent (strongly recommended for weary and sore feet), I turned back, seeing nothing more on the wing until just past the opposite hamlet of Maison-Méane, where the last rays of a belated sun woke ‘into momentary activity a few fine male EH. goante. Next day being gloriously fine, I set out for the Lac de la Madeleine, which lies on the Italian side of the Col de Larche (6545 ft.), a few hundred yards across the frontier, and about an hour and a half’s easy walking from Larche itself. Quite the commonest insect about was Macroglossum stellatarum, and wherever the sun touched the little patches of sainfoin and lucerne, Colias edusa and C. hyale were chasing one another, with P. apollo and the usual common Pierids. But I did not come across P. napi, var. bryonie; and I think that, this being a single-brooded species in the Alps, it was probably over. Push- ing on, I did not unfurl until I had reached the “‘ International House,” where the red-white-and-blue and the red-white-and- sreen posts upon the roadside denote the meeting of France and Italy. The Italian Dogana is somewhat further on by the Lake, and the affable Customs officer in command, who regarded my net as an excellent piece of fooling, not being able to direct me to any mountain path which would bring me back into the Lauzanier, I missed no doubt the best collecting ground hereabouts. For example, I failed entirely to hit the right spot for C. paleno, which I suspect occurs only on the Italian slopes, for nowhere could I discover the indispensable Vaccinium, upon which, in common with P. optilete, the larva feeds. Within a few yards of the Lake itself, however, I did come across a, to me, new and exceptionally interesting form of Hrebia mnestra, this being the variety named by Bellier gorgophone, and described by him as a distinct species (Ann. Soc. France, 1868, pp. 419-420), intermediate between H. gorge of the Alps and EH. gorgone of the Pyrenees, but later determined as a localized form of mnestra. This variety is apparently so little A BUTTERFLY HUNT IN SOME PARTS OF UNEXPLORED FRANCE. 91 known to British collectors that I think it is worth while to re- produce in brief Bellier’s account of it. ‘Male, rusty brown; all four wings traversed as to two-thirds of their breadth by a ferruginous band which mingles somewhat with the ground colour, especially on the hind wings. “Up. s. f. ws.—Band with two black white-pupilled eyes (some- times absent); h. ws. without ocellation. “Un. s. f. ws. lighter and more reddish brown, reproducing the pattern of the upper side. H. ws. reddish grey, with a broad median band of dark brown slightly lunulate ; a marginal band of the same colour. Fringes unicolorous on both sides. “Female larger than male, from which it hardly differs on the upper side, except that the brown is more yellowish and the ferru- ginous band clearer. Un.s.h. ws. much clearer grey, with two bands of reddish brown, on which the nervures show somewhat whitish. Fringes of all the wings plain and unicolorous on both sides. “Differs from gorge by the wings being more rounded, and the fringes simple, not barred. Ground colour of the under side duller in tint; band thicker, less festooned, and showing less distinctly from the ground colour.” In male specimens sent by Dr. Verity, of Florence, to the Natural History Museum from the Italian Maritime Alps, the blackish-brown androconia are very strongly marked. Bellier also notes that it prefers the green pastures like epiphron to the gorge-haunted rocks; and this is my experience, also, of the species. I may add that the plate in the ‘ Annales’ by no means does justice to the rich coloration of the var. gorgophone, except that of the figure of the under side of the male; and it is to be hoped that in some future number of his beautiful ‘ Lépido- ptérologie Comparée,’ M. Charles Oberthur will find a place for male and female figures of this very striking form of mnestra— if such it be. Curiously enough, Mr. H. J. Elwes, in his ‘ Re- vision of the Genus Hrebia’ (Trans. Ent. Soc. London, 1898, pp- 169-207), makes no mention of it either under mnestra or gorge. Of the mnestra group, in his previous ‘ Notes on the Genus Erebia’ (loc. cit. 1889, p. 333), he merely remarks that “‘ little need be said, as they are species little subject to variation and of limited distribution.” Of the Pyrenean LH. gorgone, with which Bellier associated it, Dr. Chapman says (loc. cit. 1898, p. 222), ‘‘if it is a variety of anything, it is a variety of mnestra.” But he, too, in his exhaustive examination of the male appendages of the genus, does not appear to have had any material to work out the affinities of the Basses-Alpes gorgophone. (To be continued.) 92 THE ENTOMOLOGIST. THE GENUS PdAICILOPSIS (Harrison). By J. W. H. Harrison, B.Sc. Part I.—Preuimrmnary REMARKS. As I have pointed out elsewhere, the ‘“‘ genus’”’ Biston, as represented in Staudinger’s ‘ Catalogue,’ isa very heterogeneous collection, comprising elements from no fewer than six distinct genera. These are :— Biston (Leach); type stratarius. Lycia (Hub.); type hirtaria. Ithysia (Hub.); type zonaria. Pecilopsis (Harrison) ; type pomonaria. Apocheima (H. 8.); type hispidaria. Microbiston (Stgr.); type lanarius (Ev.) (= tartaricus (Stgr.) ). It was originally my intention to take these genera in turn, and to deal with each of the species in all its stages in detail. The imagines of the genus Jthysia have already been discussed, and the treatment of the other forms postponed in order to give time for the completion of the life-histories of I[thysia grecaria, I. alpina, and I. italica, but it has been found impossible to rear (even in a hothouse) these exclusively Southern forms. In the meantime, however, I am glad to say that I have been able to secure, and describe at length, the early stages ofall of the species in the genus Pecilopsis, and therefore propose to complete my work in that section now. This genus was described in Lepid. Comp. fase. vii. p. 344, and I have but little to add to the description given there, except that one very important observa- tion has been made which justifies further my separation of these species from Ithysia. This is the fact that, whilst the chromosome number in Ithysia is 112, in Pecilopsis it is 56, and in Lycta 28. It has become imperative that I should take up this genus now, because I have discovered in the course of my studies that the Central European form that passes for P. lapponaria is not that insect at all, although, fortunately, our Scotch insect is so. Not only is this true, but, in addition, the two forms fall into two different sections of the genus, which contains four species form- ing two closely allied groups of two. These groups are :— The two species Pacilopsis lapponaria and P. rachele. The two species P. pomonaria and P. isabelle. The first group is probably Northern in its origin, for P. lap- ponaria ranges from Lapland to Livonia, and then reappears in Scotland; whilst P. rachele is widely distributed in America, from Montana and Manitoba along the Mackenzie Valley to Alaska. The other group is of Central European origin, pomo- naria having its headquarters in North Central Germany, but extending, although sparsely, to Eastern France, Scandinavia, THE GENUS P@CILOPSIS. “93 and Austria. The other species is of more limited distribution, for it is confined to the Silesian Mountains and to the Alps of Switzerland, Bavaria and the Tyrol. It will be seen that I have been compelled to erect a new species for the so-called lapponaria from the Alps and Silesia. I have tried hard to avoid this necessary split, and to persuade myself that the form is but a mountain form of pomonaria, but it will not do; there are differences of specific value at every stage of its existence—differences greater in many instances than those occurring in the case of two obviously distinct species like L. hirtaria and P. pomonaria at corresponding points. In fact, had one been so inclined, it would have been perfectly feasible to break this genus on larval differences, such as has been done in other groups, and then find this separation justified by imaginal characters. In sucha case lapponaria would fall into one subgenus whilst isabelle would fall into the other ! After these preliminary remarks, I had intended to take the species in detail, but I think it better to give a brief description of the Central European form isabelle, and then contrast it, in all the salient points, with its nearest ally pomonaria, on the one hand, and on the other with lapponaria, with which it has been so long lumped. There would be no gain in comparing it with rachele, for that insect, although perfectly distinct, is sufficiently close to lapponaria to obviate any such comparison. Pecilopsis isabelle, sp. n. (=lapponaria, auct. part.). Male.—Tone of whole insect much blacker than its congeners. Fore wings subhyaline, with the ground area before the second line feebly provided with silvery white scales. First, second and median lines present, undecided, but fairly broad; median and second lines tending to fuse toward the lower margin; second line followed by feeble white line. A zigzag subterminal line intersects the more or less dark terminal band. Veins, especially those of the cell, black ; costal groove black, mixed with orange-yellow scales. Fore wings fairly long, rownded at the tip. Hind wings hyaline, except for a few white scales at the base. Fringes narrow, black. Antenne black, not pectinated to the apex. Head reddish, collar white, thorax and abdomen black, with fairly,.broad red median stripe; patagia outlined in white. Genitalia, tip of valve rounded. Female.—Wings rudimentary, but longer than those of the other three species, provided with longish, stiff grey hairs. Body black, sprinkled everywhere, like the wings, with orange-red scales, only concentrated to form a median line on the thorax; a few scattered white scales may be present also; the whole provided with long rather coarse hair. Antenne thick, heavily grey scaled, feebly pectinated when freshly emerged. Types, one male and one female from Innsbruck, Tyrol. A table giving the points of difference between this species and P. pomonaria and P. lapponaria is appended. 94 LARVA. OVUM Young larva. .|Black, THE ENTOMOLOGIST. Pomonaria. ..e-(9mall translucent with white spots and bars Second instar|Usual form of genus Full-grown ..|Short, stout; pattern decided ; texture coarse; colour yel- lowish Isabelle. Lapponaria. Fairly large; glaucous|As in pomonaria green, more opaque &e. Green; striped mimic larch needles Pattern nearly Ground purplish. Greenish ; no spots,/As in pomonaria, but with more whitespots on spiracular stripe to|As in pomonaria the/Longer; skin texture same asin pomonaria.| fine; stripes degraded as in zonaria Larch—refuses other|Birch, Erica, Myrica gale, many trees and shrubs As in pomonaria— shorter Pattern as described. Red median stripe and white outlines of patagia very clear Food........|Oak — most forest trees foods PUPA ele aiecss's Red brown, rather] Yellower brown polished Antenne ..../Tip clear Tip clear Collar ......|Broad white Narrow white Thorax......'Pattern as in descrip- . tion of isabelle, but g coarser, and colours 4 less decided; whole a much paler 3 Fore wings ..'Long—tip rounded As in pomonaria - Fringes .. White; black spots atiNarrow; black ends of veins; fairly broad Valvesof geni- Tip rounded, as in talta: jelem crc hirtaria narrower As in pomonaria, but Pectinations indi- cated at tip Black Much broader. No pattern, medio dorsal red stripe clear; fur paler laterally Shorter and broader ; tip angular Broad ; silky dark fus- cous, like zonaria Tip with definite angle as in zonaria FEMALE IMAGO. Antenne ....|Rather thin; black |Thick; pale Thorax andjColour black, irregu-|Scales redder, simi- abdomen larly speckled with) larly scattered. Few rusty scales. Hairs} pale scales. Hairs short pale much longer and paler Wings ......|Rudimentary, very|Much longer; scales short, with rusty) redder, but some scales and few pale| almost white scales hairs present. Hairs much longer Whole outline/Long As in pomonaria of insect Thin; black Red scales definitely massed in a broad median stripe down both thorax & abdo- men; hairs pale short Variable in size, but never so long as in isabelle. Hairs darker and shorter Shorter and rounder 95 THE PSOCIDZ OF NOTTINGHAMSHIRE. By J. W. Carr, M.A., F.L.S., F.G.S. Waite collecting Hemiptera during the last two summers a good many Psocids were obtained, and as no members of this family have hitherto been recorded for Nottinghamshire, a list of the species captured may be of some use as a contribution to our knowledge of the distribution in Britain of these delicate and interesting little insects. I am indebted to Mr. Kenneth J. Morton for his kindness in examining and identifying all my captures. Amphigerontia variegata, Latr.—Common on trunk of sycamore tree in my garden at Sherwood, Nottingham; Thorney; both in August, 1913. A. fasciata, Fab. — Near Edwinstowe, Sherwood Forest, June 12th, 1912. A. bifasciata, Latr.—On hawthorn hedge, and commonly on trunk of sycamore in garden, Sherwood, Nottingham, July 17th to August 10th, 1913; swept from Callwna near Edwinstowe, Sherwood Forest, September 25th, 1918. Psocus nebulosus, Steph., and P. longicornis, Fab. — Thorney, August 15th—-19th, 1913 (L. A. Carr). Stenopsocus immaculatus, Steph.—Aspley Woods, near Notting- ham; The Dumbles, Kirkby-in-Ashfield; Upton, near Southwell, on Hawthorn: Normanton-on-the-Wolds and Plumtree, on Salix; Thorney ; taken from June 28th to September 3rd, 1913. Taken also by F. M. Robinson in Bulcote Wood, October 16th, 1913. Graphopsocus cruciatus, L.— Common. Aspley and Beauvale Woods, July, 1912; Fiskerton ; Kingston Park; West Leake Hills ; North Collingham ; Widmerpool : Sherwood Forest, near Edwin- stowe:—all in 1913 between July 25th and September 25th. Also taken by F. M. Robinson in Lambley Dumbles and at Papplewick, October 3rd—9th, 1913. Mesopsocus unipunctatus, Miill.—Aspley Woods, near Nottingham ; Sherwood Forest, near Edwinstowe: both June, 1912. Radcliffe- on-Trent; The Dumbles, Kirkby-in-Ashfield; Upton, near Southwell; Sherwood, Nottingham, June 21st to August 13th, 1913. Philotarsus flaviceps, ‘Steph——West Leake Hills, August 21st, 1913. Elipsocus westwoodi, McLach.—On trunk of sycamore tree in my garden, Sherwood, Nottingham; Arnold, near Nottingham; Upton, near Southwell; Widmerpool, on Corylus; Sherwood Forest, near Edwinstowe. Taken from July 12th to September 25th, 1913. H. abietis, Kolbe. — Edwinstowe, Sherwood Forest, June, 1912; Fiskerton, on oak; Arnold, on oak; Epperstone Park, on Pteris and on Castanea; Kingston Park, on Salix : North. Collingham, on Salix; Thorney. All J uly to September, 1913. E. cyanops, Rost.—Arnold, near Nottingham, July 24th, 1913; North Collingham, on hawthorn, August 25th, 1913. 96 THE ENTOMOLOGIST. Pterodela pedicularia, L.—Nottingham, common on windows and tables in my study, August 15th to 30th, 1913; also noticed, less commonly, throughout September. Ectopsocus briggst, McLach.—Widmerpool, on oak, August 18th, 1913. Cecilius flavidus, Steph.—West Leake Hills, abundant on oak, ash, and beech, August 10th, 1912, August 15th—21st, 1913; Hast Leake, August 11th, 1912; Edwinstowe, Sherwood Forest, August 30th, 1912; Thorney, August, 1913; Widmerpool, on oak, birch, and Salexz, August 18th, 1913; North Collingham, on ash, August 25th, 1913. “ C. burmeistert, Brauer.—Thorney, August 15th-19th, 1913 (L. A. arr). Hyperetes questfalicus, Kolbe.-—Among papers in room at Univer- sity College, Nottingham, December 13th, 1912. Troctes divinatorius, Mill.—Also among papers in same room as last species, February 10th, 1913. SYMPETRUM MERIDIONALE, Sstys, AND OTHER ODONATA. By C. W. Bracgsen, B.A., F.E.S. A Few cases of insects formerly belonging to the veteran entomologist, Mr. G. C. Bignell, of Saltash, near Plymouth, came into my possession after his death. Among them was a store-box of Neuroptera (sensu lato), collected by the Rev. T. A. Marshall, of Botus-Fleming, Cornwall, who died in 1903. On going through this recently I found a Sympetrum labelled vulga- tum, Swanage, no date. As there were no striolatwm in the box, I concluded that Marshall either intended it for the latter species, using the older name, or that he had really taken vulgatum, a rare occurrence. I sent the insect to Mr. W. J. Lucas, who is of opinion that it is neither vulgatum nor striolatum but meridionale. If so, the specimen is of considerable interest, since Mr. Lucas, in his ‘ British Dragonflies,’ says: ‘“‘ The claim of this insect to a position on the British list rests on two females of old date.’’ Most of Marshall’s specimens were Corsican, but there were several others from Swanage, including some fine Orthetrum cancellatum. It may be worth mentioning that one of the Corsican O. ce@rulescens has the left anterior wing much abbreviated. The right wing is 28 mm. long, the left only 20 mm., the pterostigma being about the same distance from the body on each side. Plymouth. 97 CONTINENTAL INSECTS OF VARIOUS ORDERS TAKEN BY DR. T. A. CHAPMAN IN 1913. wowed. loweas,. B.A. FaniS. Pupa-skin of Ascalaphus coccajus. Magnification a little over 24 nat. size. One antenna could not be withdrawn, and it is shown broken, or bitten off. The pupal-jaws are well seen; and it must be borne in mind that they were worked by the imaginal jaws that were not then withdrawn from them. The pupal-skin is very ethereal, as can easily be seen. The head has become detached from the body. Arter each of two entomological excursions to the Continent in 1918, Dr. Chapman was kind enough to give me a small collection of insects, which he was able to take, belonging to the less-known Natural Orders. In April, May, and June, he visited the Rhone valley in Switzerland and the district of the Italian Lakes, and this first collection contained insects from Sierre (1760 ft.) in the Rhone valley, from Locarno (680 ft.) on Lago Maggiore in Switzerland, and from Pallanza (680 ft.), also on Lago Maggiore, but in Italy. In July and August the scene of operations was transferred to France, and the. second collection contained insects from Lautaret (6790 ft.) and Bourg d’Oisans (2860 ft.) in Dauphiné. The former is a well-known botanical and entomological locality, and the latter is in the valley of the Rimauche, on the way up to Lautaret. My thanks are due to Mr. K. J. Morton for naming a number of the specimens. First CoLLECcTION. Plecoptera. Nemoura marginata. Locarno, April. N. cinerea. Locarno, April. 98 THE ENTOMOLOGIST. *N. lateralis. Locarno, April. N. variegata. Pallanza, May 19th—26th. Odonata (= Paraneuroptera). Inbellula quadrimaculata. Two males and three females in more or less teneral condition; Locarno, April. One male possessed strongly developed nodal spots and longitudinal saffron suffu- sion, but was otherwise normal; the others were of the var. prenubila, some being of a more pronounced type than the others. *Orthetrum brunneum. One male; Sierre, May 27th—June 2nd. Cordulia @nea. One female; Sierre, May 27th-June 2nd. Aischna isosceles. One male; Sierre, May 27th—June 2nd. Pyrrhosoma nymphula. One female; Sierre, May 27th—June 2nd. Ischnura elegans. One male; Locarno, April; one male; Sierre, May 27th-June 2nd. Einallagma cyathigerum. Two males; Sierre, May 27th- June 2nd. Neuroptera. *Ascalaphus coccajus. Four males; Sierre, May 27th-June 2nd. One of these was accompanied by the very delicate pupa-skin. In emerging it appears that one antenna stuck fast in its case (figure). It is well-developed but is broken off, the knob and part of the shank remaining in the case. Dr. Chapman thinks this is not an isolated occurrence, and that the insect, when confronted with the difficulty, itself bites off the ‘antenna. Sialis lutarva. Three; Locarno, April. - Raphidia notata. One female; Sierre, May 27th—June 2nd. Chrysopa perla. One; Locarno, April. Trichoptera. *Plitocolepus granulatus. Two; Locarno, April. *Philopotamus ludificatus. One; Locarno, April; one; Pallanza, May 19th—26th. SECOND COLLECTION. Orthoptera. Omocestus rufipes. One; Bourg d’Oisans, August 6th—-21st. Plecoptera. Nemoura inconspicua. Two females; Lautaret, July 22nd— August 5th. N. variegata. One male; Lautaret, July 22nd-August 5th. Odonata (= Paraneuroptera). Aiischna juncea. One female; Lautaret, July 22nd—August 5th. Sympetrum vulgatum. Four males and three females; Bourg d’Oisans, August 6th-2lst. Most of these were teneral in condition to a greater or less degree, and pale in colour. METAMORPHOSIS OF PHASGONURA VIRIDISSIMA. 99 Neuroptera. Hemerobius quadrifasciatus. One; Lautaret, July 22nd—August 5th Chrysopa vulgaris. Two; Lautaret, July 22nd—August dth. Panorpa germanica. One female; Bourg d’Oisans, August 6th—21st. Trichoptera. Stenophylax latepennis. One; Bourg d’Oisans, August 6th—21st. *S. ucenorum. One male and two females; Lautaret, J uly 22nd— August dth. *Metanea chapmant. Three males and one female; Lautaret, July 22nd-August 5th. This is a new species, and has been described by Mr. K. J. Morton (antea, p. 49), where details of structure are figured. Apatama fimbriata. One male; Lautaret, July 22nd—August 5th. *Sericostoma pedemontanum. One female; Lautaret, July 22nd- August oth. Berea pullata. One male; Lautaret, July 22nd-August 5th. *Rhyacophila albardana. One male and one female; Lautaret, July 22nd—August 5th. The species marked with an asterisk (*) do not belong to the British fauna. Kingston-on-Thames: February, 1914. NOTES ON THE METAMORPHOSIS OF PHASGONURA VIRIDISSIMA, L. ([OrtHoptera.] By Anprew B. Lvvont. On June 22nd of last year a female nymph of this species was obtained while sweeping some long grass in a field at Westcliff, Essex. Judging by its development after subsequent moults, it would appear to have been at about the second or third moult when captured, the ovipositor being about 8 mm. long, and the wings barely noticeable. It was placed in a cage together with an assortment of plants likely to be found in its natural haunts; such as various species of grass, dandelion, knapweed, bindweed, and one or two kinds of buttercup. The following day it was found to have been feeding freely on the common creeping buttercup (Ranunculus repens), an operation it apparently performed at night or in the early morning, as I never succeeded in observing it in the act. On visiting the locality later, from which this specimen was obtained, I found the above-mentioned plant growing in profusion, and, therefore, it seems highly probable that this is its food-plant in a state of nature. On June 25th it moulted, the ovipositor then measuring 100 THE ENTOMOLOGIST. 6 mm., and the wings 8 mm. The next moult occurred on July 10th, the dimensions increasing to—ovipositor 15 mm., wings 9 mm., and total length 34 mm. The antenne, which were damaged and of unequal length before, became normal after the second moult. It greatly appreciated being placed in the sun, leaning over on one side and extending the long jumping legs to expose as much of its body as possible. These sun-baths appeared necessary after each moult to enable it to acquire firmness and proper coloration, an operation extending over a period of about two days. For three days before a moult the nymph ceased to feed, and became sluggish and whitish in colour, somewhat after the style of a snake before sloughing its skin. The empty nymph skin was always eaten immediately after being cast, this employing the insect about an hour and a half, the skin of the large hind legs being eaten last. The final moult took place on July 31st at about 6.30 am. The imago, after eating the empty skin, clung for some time to the grass stems to allow the wings to unfold and attain their proper development. This specimen when taken in the hand would bite fiercely with the mandibles, occasionally retaining its hold until set at liberty. ADDITIONS TO THE LIST (OF KENT. APHIDIDAY By Frep. V. Turopap, M.A., F.E.S., Hon. F.R.H.S., &e. Durine the past two years I have found or identified from material previously collected the following Aphides, so far not recorded from Kent, and some of which are new to the British fauna. Several new species of Macrosiphum have been described since the previous list, and these are also included here. The year 1913 was noticeable for three things: first, the comparative paucity of the species of Aphides to be found, secondly, the presence of numbers of sexupare in the autumn months, and thirdly, the vast numbers of three or four species. Most abundant and harmful of all has been Aphis sorbi, which did untold damage to the apple crop; next in importance has been A. abietina, Walker, which has been most harmful to the Sitka and Norway spruces in Ireland and parts of the South of England, in many cases causing complete defoliation. This is one of the species which breeds entirely viviparously, no sexu- pare having been found, whilst parthenogenetic females occur right through the winter. So far no sexupare have been found of A. gossypii, Glover, the so-called Cotton Aphis, which is recorded here for the first time in Britain. Only once have I ADDITIONS TO THE LIST OF KENT APHIDIDA. 101 - found oviparous females, also of the Woolly Aphis (Hriosoma lanigera, Hausmann), and as far as recent experiments go that I have carried out, there does not appear to be any migration between the elm and the apple in this country, as has been shown to occur in America by Miss Edith Patch. Moreover, I have had one badly attacked apple tree netted for some three years, and no alate whatever have appeared. Reproduction without sexupare in some species may evidently occur for a long time. ‘The list given here does not include any fresh localities for the Aphides of Kent so far recorded (vide ‘Hntomologist,’ January, 1911, pp. 16-21, and November, 1911, and January, 1912), only new species found in the county. Genus MacrosipHum, Passerini. Macrosiphum taraxaci, Kaltenbach.—On dandelion (Leontodon taraxacum). Wye, June 17th, 1911, and July 20th, 1912; Blean Wood, July 7th, 1912. M. duffieldu, Theobald.—On tulips, March 27th, 1918. Maidstone, many alate and aptere of this beautifully marked species brought me by Mr. Adrian Duffield, and others sent by Mr. Bunyard. M. primule, Theobald.—On cultivated primulas and on the wild primrose in gardens. Maidstone, March 27th, 1913; Stouting, near Hythe, April 28th, 1913 (A. Duffield); Wye, June 26th, 1913. M. bete, Theobald.—On mangolds, beetroots, sugar beet, and several wild Chenopodiacee. Herne Bay, July 4th, 1911; Wye, July 2nd-14th, 1911; Faversham, July 4th, 1911; Dover, July 4th, 1911; Bromley, July 2nd, 1911, and Thanet generally; Tonbridge, July 26th, 1913. M. arundinis, Theobald.—On Arundo phragmitis. Wye, August, 1912; Romney Marsh, July 17th, 1913, in small colonies. M. graminis, Theobald.—On meadow foxtail and Timothy grasses; Wye, August 23th, 1911, evidently very uncommon. M. rubiellum, Theobald.—On bramble (Rubus fruticosus) and raspberry (f. ideus), Mayto June. Wye, Ashford, Paddock Wood, Tonbridge, Maidstone, Ramsgate, abundant. M. malve, Mosley. — On Malva sylvestris and Malva, sp.? Wye, June 7th, 1913, two alate females. M. trifolti, Theobald.—On T'rifolium procumbens. Wye, August, 1912, in small numbers. M. loti, Theobald.—On Lotus corniculatus. Wye, July and August, 1912 and 1913. Alate and aptere in the last year. M. stellarie, Theobald.—On Stellaria, spp. Wye, May, 1912. I found this species in vast numbers in alate form at Bramley, in Surrey, in May, 1913. This was erroneously placed under Schrank’s name (Entom. December, 1911). 102 THE ENTOMOLOGIST. M. crategarium, Walker.—On hawthorn. Wye, June 7th, 1911, and July Ist, 1911. M. sileneum, Theobald.—On Silene inflata. Wye, July 10th, 1911, and August 14th, 1912.