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MN) ~"S ae yi Mitty = tt ‘ A it alee Ann dy aS er | Vite. 4 4 'sSupnannee TOLLE pion TESTE 4 me PEN rt Op LPN oo eae ‘ mronmen MO Nal lias cia LAL Ll jae) resayt s fi J “Os Cyt, hel as Bile tgs Mee e cd Pete Pm steer niin Sait: m : wes Ar yp ai 1) bs | K sl ett. vga! w . \ Ty AL \ HLL Ww Se Af an wt . $44 g: aM oo Sey tinatidl Tages OR MM gee ren’ rh e s74 -) Ly eWay Bid Adah || || Fey Pe aN Hey psesoant MMS « . te Vv Vey Bee Al). aN ‘ a] rel ry 4 Ci. | im | Shed rm i ~ 34 ' ATT vf ivy OG. ag itty Th Pe iy og tt ; ig Wye Ady, * Ves me - 4 at} 13 , : 1S Re 7 “iG yeveg + OFS Bla | * ¥ Sh p>) wv iy, * ery prs i soy a BE dalaatabLaledy wet att ae “ig it eq, . Wh 1 | mh ~ PEG Pee yo wy Co Wyeee (i +4 Yeiiiilinl Serenity tkang thi scngrt yee A KS AGS ae 7 TV RERLEE Bw endtiamedtad ynedt 19 Vatu - wT phy share "hh A | STEPH Pe Te : PP Bsr ie Se ea Pie ua) niin " sedi a ay i Hu a ih PROCEEDINGS OF THE GENERAL MEETINGS FOR SCIENTIFIC BUSINESS OF THE © AVOLOGICAL SOCIETY OF LONDON. 1918, pp. 1-196, witH 1 PuatTe and 32 TExr-FIGURES. ye a “axnsonian Instity rA\S %, ‘ $tional Musev™ + PRINTED FOR THE SOCIETY, SOLD AT ITS HOUSE IN REGENT’S PARK. LONDON: MESSRS. LONGMANS, GREEN, AND CO.,, PATERNOSTER ROW, IS Ie OF THE COUNCIL AND OFFICERS OF THE ZOOLOGICAL SOCIETY OF LONDON. MIS Patron. His Magesty Tue Kine. COUNCIL. | His Grace Tue DuKe or Beprorp, K.G., F.R.S., President. Tue Hon. Cecit Barrne, M.A. | Ricuarp H. Burne, Esq., M.A. Lr.-Cout. S. Moncxron Copr- | MAN, M.D., F.R.S. CuarLes Drummonn, KEsq., Treasurer. ALFRED Ezra, Esq., Vice- President. Carr. HAroLp S. FERGUSON. Cart. Huau §. GLADSTONE, M.A. Sipney F. Harmer, Esq., M.A., Sc.D., F.R.S., Vice-President. Pror. JAMes P. Huu, D.Sc., F.R.S. WituiAM Huntsman, Esq. Str Epmunp G. Loprr, Br., | Vice-President. Ne f u . a ¢€ ety ey y = a * ‘ Pror. Ernest W. MacBripe, D.Se., LL-D., F.R.S., Vice- President. Con. Sir A. Henry McMaunon, G.C.M.G., K.C.L.E.,G.C.V.O., C.8.1. P. CuaumMers MircHey, Esq., MOA DSc? LD. HIRES O.B.E., Secretary. ApriAN D, W. Pottocr, Esq. Tue LorD QUEENBOROUGH. Toe Marquess of Siigco, F.S.A., Vice-President. AuByN Treyor-BatryE, Hsq., M.A. AntrHony H. WINGFIELD, Esq. A. SmiraH Woopwarp, Ksq., IID ag IDSIRaS, egleing- sident. PRINCIPAL OFFICERS. P. Cuatmers Mitcuent, M.A., D.Sc., LL.D., F.R.S., O.B.E., Secretary. R. I. Pocock, F.R.S., F.L.8., Curator of Mammals and Resident Superintendent of the Gardens. D. Sera-Suiru, Curator of Birds and Inspector of Works. Lieut. Epwarp G. BouLencer, Curator of Reptiles. Prof. H. Maxwett Lerroy, Curator of Insects. JouNn Barrow, Accountant. W. H: Cots, Chief Clerk. LIST OF CONTENTS. 1918, pp. 1-196. EXHIBITIONS AND NOTICKS. The Secrerary. Report on the Additions to the Society’s Menagerie during the months of November and iDyerersrmnl oye, WIG Goo nsoconnsoonosenadaee saga ond0nddoonDboands Mr. D. Seru Suiru, F.Z.S., Curator of Birds. Exhibition of; and remarks upon, a series of lantern-slides made from photographs of Reptiles taken in the Gardens... Dr. P. Cuaumers Mircuent, F.R.S., Secretary to the Society. Communication of a letter from Mv. T. E. Whitehead on the Wild Dingo ...........--...:esseeee ees Dr. R. Broom, C.M.Z.8. Exhibition of, and remarks upon, a New and a Rare Species of the Golden Mole......... The SECRETARY. Report on the Additions to the Society’s Menagerie during the month of January, 1918 ...... Dr. Smrra Woopwarp, F.R.S., V.P.Z.8. Exhibition of a eopy of an incised drawing of a hunted deer............ Professor Povunron, F.R.S:, F.Z.S. Communication of a letter from Captain G. D. Hale Carpenter on an African Civet attacking Human Beings ............... Professor E. W. MacBripe, M.A., DSc., F.R.S., F.Z.S. An account, illustrated by lantern-slides, of his recent investigations into the development of the Sears Wee bina pee hy cee eee aici onde lors a weratoeie bislarerciaiaieiere’s Mr. D. Sers Surru, F.Z.S., Curator of Birds. Exhibition and description of skins of the Hoatzin, illustrated by lantern-slides 2. ...5.2..4.9.casedet se seeescienecler ee eesens Page 187 187 188 189 190 191 191 192 iv Mr. C. Tare Regan, M.A., F.R.S., F.Z.S. Exhibition of photographs of an Indo-Pacific Chetodont Fish. (lest torsos 128. se clraae tte An cioe a ame ee ete The Secrerary. Report on the Additions to the Society’s Menagerie during the months of February and JUTE aCe) O15 2 OS) Rol een nl CPAP NALA EOR GH STRA ama Sw ao Miss L. EK. Cunrsman, Assistant Curator of Insects, Exhi- bition of specimens of an Kast-African homopterous IDS Cbs se oy 8 Se areca nT as eR DO Dr. A. S rru Woopwarp, F.R.S., V.P.Z.S. Exhibition of, and remarks upon, the fossil rostral teeth of Hopristis CHAKA de RETO ee eee CROCE OS coger uM na Nome wea yCRemacohonee Mr. G. A. BouLtencrr, F.R.S. Exhibition of the head of a Congo Mish) Hydrocyon goliath.) see Mr. D. Sera Suire, F.Z.8., Curator of Birds. Exhibition of, and remarks upon, a Zulu Head-dress............... Dr. P. CHatmers Mircuenn, F.RB.S., Secretary to the Society. Remarks on an advertisement announcing Minis Sales amenhegWmitedmstatesum sre an annem ae Professor. Woop-Jonus, F.Z.8:, Honorary Acting Prosector. Exhibition of, and remarks upon, specimens from the Prosectorium illustrating the effects of Rickets PAPERS. —— eee 1. Skull of Rana tigrina Daud. By B. L. Buatta, MESes and Barnt Prasnuap, M.Sc. (Assistant Professors of Zoology, Government College, Lahore). (‘Text- figures 1—9.) suns niese S880) [8)8 eho nelelalaleliei etal sveletefelolefelelslelefelelevelelelalatelsteherereiere 2. Description of a new Snake of the Genus Oligodon from Upper Burma. By G. A. BoutencEr, E.RS., F.Z.8. (Text-figure 1.) hi OO See CCN a) psu) . Reptiles from the River Tajan (Transcaspia). By L, A. Lantz. (Plate I.) ee a Page 194 194 195 195 196 Alphabetical List of Contributors Vv . On the External Characters of the Lemurs and of Tarsius. By R. I. Pocock, F.R.S. (Text- MEMES WING) sacnesaasossesesso0 2000000 ospapegscosecpaceddes _ A Classification of the Pyratrpm, subfamily Hyrso- TROPIN#. By Sir GeorcE Hampson, Bart., F.Z.S. ... }. First Report on the Inheritance of Visible and Invisible Characters in Silkworms. By Miss Maupe Hn) CHRETIORIN: MZ ashy Its! UiiSom Wold beh aosppagodcasasongsede . Notes on Cetacea stranded on the British Coasts during 1913-1917. By Srpxey F. Harmer, Sc.D., F.B.S., F.Z.8., Keeper of Zoology in the British Museum (Natural EMIS tory, yore cone ep ae erie ais enocee co uidecmns se . On the Variation of the Pit- Viper, Lachesis atrox. By Miss Joan B. Procrsr, F.Z.S8. (Text-figures 1-5.)... . Report on Deaths of Animals in the Gardens in 1917. By J. A. Murray, M.D., B.Sc., F.Z.S., Director, Imperial Cancer Research Fund, Pathologist to the Society . Bam me ees sees ererseseseesereess essere sesesesesees oer soeene eee verses oscese nesses oesneseseser weet PP Set osoersoserereserssssreseressesoosnosseeeresseoeseoseneressens Page 19 59 133 147 163 yu a ah hae * AN ae AGS aii CAC SiS) OF THE CONTRIBUTORS, With References to the several Articles contributed by each. (1918, pp. 1-196.) : a Page Buatta, B. L., M.Sc., and Barnt Praswap, M.Sc. Skull of Rana tigrina Daud. (Text-figures 1-9.) ...... 1 Boutencer, G. A., F.R.S., F.Z.8. Description of a new Snake of the Genus Olzgodon from Upper Burma. (Text-figure 1.)........................ 9 Exhibition of the head of a Congo Fish, Hydrocyon GOULAEIE yes. eck Ee Ree talent ave ISIE
en(Rext=tig ures) acgse epeecaesascee os: seers 192 Sera Smirx, D., ¥.Z.S., Curator of Birds. Exhibition of, and remarks upon, a series of lantern- slides made from photographs of Reptiles taken in the Gandenst tec. ..seceacne Ae haces a deta dear cares rhage 187 Exhibition of, and remarks upon, a Zulu Head-dress... 195 W oop-Jones, Professor, F.Z.8., Honorary Acting Prosector. Exhibition of, and remarks upon, specimens from the Prosectorium illustrating the effects of Rickets ............ 196 Woopwarb, Dr. Suits, F.R.S., V.P.Z.S. Exhibition of a copy of an incised drawing of a hunted CGC Teac gee ato secs e eneias SESE SE OUNOREE URE ESE OBE aan ie aa 19] Exhibition of, and remarks upon, the fossil rostral heethiol Ho pristis: andi tr0siisi tech ue ene ae ees eaten tone 194 Proc. Zoou. Soc.—1918. b pe rate AeA petgh iy tit ‘dt er wine’ oe sea Pemiorngs h Leow (au Solent oe By ceEpe evar ADRSaeerd oe 4 SP asiiyi 0; 5 I e ; ‘Whos ay: hada be Tt uit p es ‘ SSS PP Khe Cees INDEX. 1918.—Pages 1-196. 4 [New names in clarendon type. Systematic references in italics. (z.8.U.) indicates additions to the Society’s Menagerie. | Agama sanguinolenta, 14. Alamosa bipunctella, 65. piperatella, 65. Anerastia ablepta, 88. acrophea, 88. anemopsis, 88. argosticha, 88. — baliora, 88. ephestiella, 88. ——— erasmia, 88. »« korbi, 79. —— pleurochorda, 88. awiphimela, 88. Aptenodytes patagonica (z.s. u.), 194. Atascosa quadricolorella, 104. Aurora longipalpetla, 106. AVES: Head-dress made of plumes of Chere progne, 195. Axis porcinus (z. 8. L.), 194. Balenoptera acutorostrata, 148. borealis, 149. physalus, 151. Balearica pavonina (z. s. L.), 195. Bandera binotella, 89. carneella, 90. Bandera cupidinella, 90. perlepidella, 90. — subiuteella, 90. —— virginella, 90. Baptotropa, gen. n., 116. tricolorella, 116. Barberia affinitella, 181. Bematiscus lesche ; exhibited, 189. Biafra concinnella, 115. — rhodinella, 115. Bison americanus (z. s. .), 193. Boiga-trigonatum, 16. Cabnia myronella, 131. Calamotropa, gen. n., 91. pulverivena, sp.n., 91. Calera punctilimbella, 59, albicostella, 62. Canis familiaris, communication, 188. Carduelis caniceps (z. 8. L»), 187. Carphibis spinicollis (z. s. u.), 191. Ceara albifasciata, sp. n., 63. -— discinotella, 63. Chere progne: exhibited, 195. Chortoneeca, gen. n., 80. eurysticha, 81. eee leucocraspia, sp. n., 81. Proc. Zoot. Soc.—1918, No. XLV. 14 Xi Chortoneca minimella, 81. SSS minoralis, 8 ] . Chrysochloris selateri: exhibited, 190. Cenochroa californiella, 59. illibella, 58. inspergella, 59. -— monomacula, 59. Coenotropa, gen. n., 89. —— limitella, sp. »., 89. Commotria albinervella, sp. u., till —— arrhabdella, sp.n., 108. ——- castaneipars, sp. n., 112. crassiscapella, 110. —— enervella, sp.n., 112. —— erythrograpta, sp. n., 109. invenustella, 108. laticostella, 108. —— mesiella, sp. n., 108. | —— miosticta, sp. n., 110. —— neurias, sp. n., 109. | -— oberthuri, 108. opacella, 108. —— phlebicella, sp. n., 112. —— pheenicias, sp. n., 110. —— phycitella, 109. —— propheella, sp. n., 112. — rhodochroa, s).n., 111. ——-. rhodoneura, sp. n., 110. | —— rosella, sp. n., 111. —— roscopennella, 108. —— rufidelineata, sp. n., 110. —— rufimedia, sp. n., 109. —— tripartella, sp. n., 109. -—— venosella, sp. n., 111. Coracopsis nigra (z. 8. L.), 187. Coscoroba cescoroba (z. s. t.), 187. Critonia hilgertt, 121. —— holorhoda, 120. -— leucopleura, sp. n., 120. ochracéalis, 121. —— pheoneura, sp. n., 119. promelena, 120. —— purpureotincta, 120. — rhodessa, 121. roseistrigella, 120. —— sarcoglauca, 121. INDEX. Critonia sarcoida, sp. n., 121. subconcinnella, 120. Cygnus melanocephalus (z. 8. .), 187. Delphinus delphis, 159. Dembea venulosella, 64. Discofrontia normella, 119. Eechinoecardium cordatum: lJantern- slide, 192. Ematheudes crassinotella, 115. euchlytelia, 115. —— lentistrigalis, 114. —— paleatella, 114. pseudopunctella, 114. punctella, 114. straminella, 114, - tunesiella, 114. varicella, 115. vitellinella, 115. Emmalocera actinoleuca, sp. n., 127. albicostalis, 131. — anerastica, 129. —— aurifusella, 128. — bifidella, 128. —— carnatella, 130. —— costella, 130. * —— cremoricosta, 1380. depressella, 128. —— diversella, 130. —— endopyrella, sp. n., 127. — eremochroa, sp.n., 130. erythrinella, 180. laminella, 129. latilimbella, 129. — leucocincta, 128. longiramella, 127. — lucidicostella, 129. — monochromella, 130. ornatella, 127. —- polychroella, sp. n., 128. —— pulvereatis, 127. —— radiatella, 127. sanguifusalis, 128. —— strigicostella, 128. INDEX. xi Emmalocera subfasciatella, 151. | Halicherus grypus (h. . 1), 187 — tricoloraiis, 130. : —— uimbricostella, 129. Holacanthus seimicirenlatus (Fig. 1), photograph, 192. —— umbrivittella, 131. | Hosidia ochrineurella, 64. —— variegateila, 129. Hydrocyon goliath ; exhibited, 195. Epidauria chionocraspis, sp.n-, | Hyperoodon rostratus, 153. 92. Hypsotropa acnidias, 77. — discella, 92. — adumbratella, 73. . —— perfasciella, sp. n., 92. —— albivenalis, 70. —— pheniceella, 92. —— approximella, 77. strigosa, 92. — hipartella, 78. —— subcostella, sp. n., 93. | —— biscrensis, sp. n., 69. —-- transversariella, 92. | —— castella, 78. Eremias intermedia, 14. gener j a i - — (Mesalina) guttulata, 15. eee See ease +— velox velox, 14. | —— cremoricosta, sp. u., 7+. Eryx miliaris, 17. — diaphza, sp. n.. 79. Ethiotropa, gen. n., 116. —— dyseimata, 75. pyromerella, sp. n., 116. —— endorhoda, sp. n., 76. ETHOLOGY. — | —— euryzona, 75. Insecta: Exhibition of specimens —— fuscostrigella, 68. of an East-African homopterous __. fusifasciata, sp. n., 71. insect, 194. | —— graptophlebia, sp. n., 76. Eudocimus ruber (z. s. t.), 191. | —— heterocerella, 68. Eumeces schneideri, 15. | icasmopis, 75. scutatus, 15. ichorella, 72. —— illectalis, 69. Felis chaus (2. 8. t.), 194. waiematellsL, 1k. Fondunkia translucidella, 131. ee aa it Fossifrontia leuconeurella, 107. See ie —— leucocraspis, sp. n., 77. leucophlebiella, 77. Genneeus swinhoii (z. s. u.), 191. —— limbella, 71. GEOGRAPHICAL: ——— luteicostella, 70. Insecta: An East-African homo- | —— monostidza, sp. n., 76. pterous insect from Nairobi, 194. neurica, 78. Mammatra: On Cetacea stranded on | ——- niphopleura, 75. the British Coasts, 147. —— niveicosta, sp n., 74. Pisces: Head of Hydrocyon goliath | ——— ochricostella, sp. n., 70. from the Congo, 195. ~ —— ocraceella, sp. n., 69. Rertitia: Reptiles from the River | papuasella, 73. Tajan, 11. —- paucipunctella, 72. Globicephala melena, 157. —— periphza, sp. n., 74. Gorgon taurinus (z. 8. L.), 187. ——— pervittella, sp. n., 68. Grampus griseus, 157. phyrdes, 73. Gymnodactylus caspius, 14. polyactinia, 70. microlepis, sp. n. (PJ. I. fig. 1), .—— polystictella, sp. n., 77. ie | —— punctinervella, sp. n., 72. X1V INDEX, Hypsotropa purpurella, sp.u.,71. [NSE Or pusillclla, 73. psamathella, 70. quadripunctella, Tb. ramulosella, 76. rhodochroella, sp. n., 69. rhodosticha, 77. ToOsescens, sp. u., 79. sabuletella, 73. seeletella, ‘72. semirosella, 69. solipunctella, 72. stereosticha, 75. subcostella, sp. 1., 68. syriacella, 72. tenutcostella, 69. tenuinervella, 73. tripartalis, sp. n., 7 wnipunctella, 71. vertheimsteint, 72. - vulneratella, 72. zophopleura, 71, cra. 1 the Pyralidx, subfamily Hypso- tropine : systematic, 55; On visible and invisible characters in Silk- worms: structure, 183; On an Hast-African homopterous insect, 194. Ityrea nigrocincta: exhibited, 194. Lagenorhynchus aculus, 158. allirostris, 158. Laurentia albivenella, sp. n., 90. inclarella, 91. Leotropa, gen. »., 64. Lopl Lutr Mab papuanensis, sp. n., 65. phoenicias, sp. n., 64. sarcina, sp. n., 64. 1ophorus jmpeyanus (z. s.u.), 191. w lutra (z.s..), 191. uia septenteniata, 10. MAMMALIA. Skull of Rana tigrina: structure, 1; External Characters of the Lemurs and of Zarsius: structure, 19; On Oetacea stranded on the British Coasts: structure, 147; Communi- cation of letter on the Wild Dingo, 188; On a new species of the Golden Mole: structure, 189; On the rare Golden Mole, 190: Copy of drawing of a hunted Deer, 191 ; On an African Civet attacking Human Beings, 191: On Fur Sales in the United States, 195. Martia arizonella, 118. Megalophota, gen. v., 117. —— leonella, sp. n., 118. Menuthia navella, 61. Mesodiphletia crassivenia, 62: -—— deliquella, 62. ~—— ochraceella, sp. n., 62. rosella, 62. stricticostella, 62. Mesoplodon bidens, 15d. Metacrateria, gen. n., 79. —— metallaciis, '79. Miasticta, sp. n., 79. — rerirrorella, sp. n., 79. —— pulverulella, 79. Monoctenocera brachiella, 122. —— leucania, 122. MorpPuHoLoey. See STRUCTURE. Nasua narica (z. 8. .), 190. Nuti ia tessellata, 17. Navasota chionophlebia, sp. n., 66. —— discipunctella, sp. n., 67. -~—— hemapheeella, sp. n., 66. ~—— hebetella, 66. leuconeurella, sp. n., 66. —— myriolecta, 67. —— persectella, sp. n., 66. —— syriggia, sp. u., 67. Oligodon hamptoni, sp. n. (Fig. 1), 9. INDEX. XOVi as Ollia honoponerelia, 104. parvella, 104, santartiella, 104. Orcinus orca, 156. Osacia lineolella, 123. Oxyrhopus cleelia: lantern-slide, 188. PATHOLOGY. Animals in the Society's Gardens, 188. Patna brunneicostella, sp. n., 117. —— eboricostella, 117. —-— venatella, sp.n., 117. Pectinigeria pamponerella, 104. -— violodis, 104. Peoria albidella, 78. Phocena phocena, 159. Phenicopterus chilensis (z. 8. L.), 187. —— roseus (%. 8.1..), 187. Physeter catodon, 151. PIscus. On the development of the Sea- Urchin, 192; A Cheetodont Fish with Arabic characters, 192; On fossil rostral teeth of Eopristis and Pristis, 194; Exhibition of head of a Hydrocyon goliath, 195. Polyocha achromatella, sp. n., 126. ——. cinerella, 125. detritella, 126. — flagrantella, 125. —— foucarti, 126. ; —— fuscicostella, sp. n., 126. gensanalis, 125. leucopleurelia, 124. —— neuropterelia, 126. —— plinthochroa, sp. n., 124. —- rhodesie, 131. ——- sanguinariella, 125. —— stipella, 125. — strigivenella, 125. —— venosa, 125. —— vesculella, 125. Polyplectruim chinquis (z. 8. u.), 191. Powjadia cyttarella, 104. — leuconewra, 104. Powjadia pimella, 104. Prinanerastia incarnatella, 80. —— lactealis, 80. — lotella, 80. nitidicostella, 80. Prophtasia amplichea, sp. n., 105. —— bistriatelia, 106. —— epiteuxis, sp. n., 105. -—— glaucophza, sp. n., 105. -—— platycerella, 104. —— pyrostrota, sp. n., 106. -_— sphalmatella, sp. n., 105. Ragonotia dotalis, 124. Raphimetopus, gen. n., 78. —— ablutella, 78. —— spinifrontella, 78. REPTILIA : On a new Snake of the Genus Oligodon : systematic, 9; Reptiles from the River Tajan: systematic, 11; On the variation of the Pit- Viper: structure, 163; Lantern- slides made from photographs of Reptiles, 188. Rhinaphe apotomella, 82. — approximella, sp.n., 82. biseriella, 85. brunneovittella, 85. castanealis, 83. —— celselia, 83. -—— conspersella, 86. ella, 86. —— enervella, 84. —— endonephele, sp. n., 87. —-— flavescentella, 84. -—— furvimacula, sp. n., 87. haploschema, 84. —— hemirhodella, 85. — holophea, 8:3. —-— ignetincta, sp. n., 87. —— infumella, 86. —— lateritiella, sp. n., 86. —— leucoteniella, 85. ——- lotricella, 85. —— mictochroella, 87. neesimella, 83. Xvi thinaphe nigricostalis, 83. ——- pailidicosta, 84. —— pheostrotella, sp.n, 85. plinthina, 83. —— sangirensis, sp. n., 85. --— secholdi, 87. -—— separatella, 84. —— signicollis, 87. —— stictella, 84. —— syssema, 86. ------ taliella, 86. —— vectiferella, 88. venelia, 83. — venilineella, sp. n., 86. —— virginella, 84. Rhodochrysa superbella, 89. ¥ Sabormania pia, 131. Saborina forcipella, 122. -—— papuacola, sp.n., 123. vicina, 123. Saluria albivenella, 99. —— anchridis, 98. -—— arcticostella, 100. ardiferella, 99. hreviculella, 101. callirhoda, 103. —— cancelliella, 102. ——— carnescens, sp. n., 94. —-— claricostella, 95. ctenucha, 94. —— Gesertella, sp: n., 97. —— devylderi, 100. —-- dichroella, 101. —— distictella, sp.n., 101. ensiferella, 102. erodella, 98. jflammella, 94. ——- flavicosta, sp. n., 96. — Jenrkompsoaersill, ps n., 98. —— floscella, 96. —- furvella, 100. —— gemmatella, 100. —— glareosella, 95. ——— grammivena, sp. n., 99. —— hemiphealis, 94. —— holochroa, 102. INDEX. Saluria inficita, 96. —— insignificella, sp. n., 103. — interpunctella, sp.n., 103. — lentistrigella, sp. n., 97. —— macrella, 100. —— maculivittella, 102. magnesiella, 103. —— mesomelanella, sp. n., 103. —— minutella, 95. -— museella, 28. = neotomella, 101. —— neuricella, sp. n., 98. —— nigritella, 99. —— nilgiriensis, sp. n., 95. -— ochridorsella, 97. —— opificella, 101. ostreella, 102. paranensis, 98. —— paucigraphella, 94. pectigerella, 102. pleurosticha, 98. -—— proleucella, sp. n., 99. —— psammatelia, sp. n., 94. pulverosa, 102, —— rhodophea, sp. n., 100. rosella, 97. -—— rufella, sp. n., 101. —— semirosella, sp, n., 94. —— sepicostella, 99. —— spurcella, 96, —— stictella, sp. n., 96. ——- stictophora, sp. n., 96. —-— subcarnella, 100. -—— subcostella, sp. n., 100. —- tenuicosta, sp. n., 98. tetradella, 102. —— triparteila, 108. —— varicoselia, 99. verecundella, 97. Schenectadia merilesella, 131. Schlegelia wilsont (%. s. u.), 187. Siboga albimediella, sp. n., 113. —— dialeucella, sp. n., 113. —— falsella, 113. zeavora, sp. n., 113. Statina hifasciella, 60. cashmiralis, 60. —— gaudiella, 60. ° : INDEX. Statina punctitineella, 60. rhodobaphella, 6\). roseotinctella, 60. —— rosinella, sp. n., 60. STRUCTURE. Insecta: On visible and invisible characters in Silkworms, 133. Mamnania: Skull of Rana tigrina, 1; External characters of the Lemurs and of Tarsiws, 19; On Cetacea stranded on the British Coasts, 147; On a new species of the Golden Mole, 189. ReptintA: On the variation of the Pit-Viper, 163. Sudania subcostella, 88. Tampa dimediatella, 63. Taphrometopon lineolatum, 16. Xxvil ‘Tetrapteryx paradisea (z. s. L.), 193. Tinerastia discipunctella, 61. Jissirella, 61. Tursiops truncatus, 157. VARIATION: ReptiniA: On the variation of the Pit-Viper, 163. Pisces: A Chetodont Fish with Arabic characters; On fossil ros- tral teeth of Eopristis and Pristis, 194. Vipera lebitina, 15. Zamenis diadema, 16. rhodorahchis, 16. Ziphius cavirostris, 154. PRINTED BY TAYLOR AND FRANCIS, RED LION COURT, FLEBY STRERT, By PROCEEDINGS OF THE GENERAL MEETINGS FOR SCIENTIFIC BUSINESS “ZOOLOGICAL SOCIETY OF LONDON, 1918. PARTS I. & Thine, nso CONTAINING Paces 1 to 196, witu | Prate AND 82 TEXT-FIGURES. AUGUST 1918. PRINTED FOR THE SOCIETY, SOLD AT ITS HOUSE IN REGENTS PARK. : LONDON : : MESSRS. LONGMANS, GREHN, AND CoO., PATERNOSTHR ROW. [Price Twelve Shillings. | ris Bae .< f y od LVS Ot 30. NEN Die: 1918, Parts I. & II. (pp. 1-196) EXHIBITIONS AND NOTICES. Page The Secretary. Report on the Additions to the Society’s Menagerie durimg the months of November and..December.alOl7 siieestocet cee Se ei ee ee 187 Mr. D. Suru Smitu, F.Z.S., Curator of Birds. Exhibition of, and remarks upon, a series of lantern-slides made from photographs of Reptiles taken in the Gardens ........ 187 Dr. P. Caatmers Mircuntn, F.R.S., Secretary to the Society. Communication of a letter from Mr. T. E. Whitehead onthe Wild Dineor ..4e J 25. 5 Gee oe ee 188 Dr. R. Broom, C.M.Z.S. Exhibition of, and remarks upon, a New and a Rare Species of bie Golden Mole .si2i 2.205 Habs: Nat 4 iis Potent 4 wee oe een eet 183 The Sucrerary. Report on the Additions to the Society’s Menagerie during the month Of danuary,, ROG s crac acs aiete cies eee epee Siete ee, RRC ee tant ieee parca LE Dr. Suir Woopwarp, F.R.S., V.P.Z.8. Exhibition of a copy of an incised drawing ofa | hunted deer’ cess 27. Gracin cine te cin aes See te eee ne arte eee 191 Professor Povutron, F.R.S., F.Z.8. Communication of a letter from Captain G. D. Hale Carpenter on an African Civet attacking Human Beings ...........0000.-.00000 191 Professor E. W. MacBripu, M.A., D.Sc., F.R.S., F.Z.S8. An account, illustrated by lantern-slides, of his recent investigations into the development of the Sea-Urchin.. 192 Mr. D. Sera Situ, F.Z.S., Curator of Birds. Exhibition and description of skins of the Hoxsizin} allustrated:bylantern-slides (s,s: hece eee ee eee Peel Oe Mr. C. Tavs Rugan, M.A., F.R.S., F.Z.8. Exhibition of photographs of an Indo-Pacific Ohxtodont Fish." (Dext-feure 1) o.0 5, 20. te oe ee ee 192 The Srcrurary, Report on the Additions to the Society’s Menagerie during the month of Hebruanye dol 8 sic tiara ae ke Ik eee iatradatvdiele Guicy euaontnn ert ward tan saan ae neat 193 Miss L. E. Cunnsman, Assistant Curator of Insects. Exhibition of specimens of an Hast- Afrieanshomopterous insect ~... 0.00.0 s sn oe cies SO eee ee Dr. A. Surra Woopwarp, F.R.S., V.P.Z.S. Exhibition of, and remarks upon, the fossil rostral teeth of Hopristis and Pristis ...... <'eSiai eitelau sh ouehes Umeua ebch a tape omelet car Rataaan cesta case 194 Contents continued on page 3 of Wrapper. PROCEEDINGS OF THE GENERAL MEETINGS FOR SCIENTIFIC BUSINESS OF TIT ZOOLOGICAL SOCIETY OF LONDON. PAPERS. 1. Skull of Rana tigrina* Daud. By B. L. Buarta, M.Se., and Baint PrasHap, M.Sc. (Assistant Professors of Zovlogy, Gav conmene College, Lahore)+. Acgirsonian nstyt, alos FEB 17 1920 Length of head and body — 0°48 to 0°51; average 0°50 0° 49 to 9°51; average 0° 50 Length of hind limb Length of head and body = 0°69 to 0°73; average 0°71 0°65 to 0°70; average 0°68 The comparison with the corresponding data of G. microlepis shows the difference in the length of limbs*. Besides G. lon- gipes has 12 to 15 supralabials, and the first pair of chin-shields. almost always forming a suture behind the mental; on one- specimen only out of 14 these plates. are separated by two small scales. As to the size of the tubercles of the head, neck, and back, the scaling of the throat and belly, the number of femoral and preeanal pores, the two species seem to agree. There is a very interesting gradation in the characters of ‘scaling between the three species G’, microlepis, G. fedtschenkoi, and G. caspius. G. microlepis has the smallest and the most numerous scales, its tubercles are relatively feebly developed ; G. fedtschenkot forms the link between the foregoing and G. cas- pius, which has the largest and the least numerous scales, and | very strongly developed tubercles. The following table con- tains the most important distinctive characters of these three species :— ; ; G. microlepis. G. fedtschenkoi +. G. caspius f. Tubercles of the temple ... moderately conical. conical. trihedral. Before the ear-opening ... ... 2 or 3 small tubercles. 2 or 3 small tubercles. 1 large tubercle. On the neck ................., slightly conical scales. moderately prominent very prominent large. ; trihedral tubercles. trihedral tubercles. Tubercles of the back ...... moderate, prominent, large,. prominent, not very large, very promi-- not spmose. spinose. nent, often spinose. Guuilatiscales=ssssesee asses extremely small. very small. small. Number of scales in a line | between the apex of the | mental or the suture of > 136 to 144. 123 to 131. 100 to 114. the chin-shields and the | analuclerginare ru) Number of Bea “seales ) across the middle of the - 35 to 38. 30 to 338. 24 to 29. belly ALi) Suprafemorals on the inner 2 small, smooth, or in- moderate, distinctly large, strongly keeled. side of the thigh ......... ) distinctly keeled. keeled. Number of femoral and) 34. to 39. 26 §. preanal pores ............ 9 * Nikolski attributes as a distinctive character to G. longipes the greater diameter of the eye, which he supposes to be longer than the distance from eye to nostril ; with this statement Mr. Lindholm does not agree. + Material: 2 ¢ from Samarkand. ¢ Material: 2 9 from Shemakha (Caucasus); 5 spec. (2 ¢, 12, 2 juv.) from Sangatshaly near Baku (Caucasus): 3 spec. (1¢,22) trom Askhabad (‘Transcaspia), 1 g¢ trom Anat (Transcaspia), and the 2 described here trom the river Tajan. * § 24 to 84 ventral scales and 30 to 37 pores, according to Nikolski, Fauna of Russia. Reptiles I., Petrograd 1915, p. 78. || The maximum is 30, according to Nikolski, Joc. cit. p. 74. 14 MR. L. A. LANTZ ON 2. GymNopactyus caspius Eichw. (PI. I. fig. 3.) 12. Length of head and body 65mm. 9/10 supralabials, 7/8 infralabials. 14 longitudinal rows of dorsal tubercles. 65 dorsal scales in a transverse row across the middle of the body. 101 scales in a line between the suture of the chin-shields and the vent. 28 ventral scales across the middle of the belly. 3. AGAMA SANGUINOLENTA Pall. 4 specimens, agreeing in every respect with others from Transcaspia (Askhabad, Anat, Bairam-Ali). Length of head and body 83 mm. (¢), 81 mm. (¢), 78 mm. (9), and 36 mm. (juv.). 14 to 17 supralabials, 15 to 17 infralabials. 43 to 47 gular scales and 73 to 76 ventral scales in a line from mental to vent. 58 to 64 dorsal and ventral scales round the middle of the body. The young differs from the adults in having no spinose scales. 4, KREMIAS VELOX VELOX Pall. 2 specimens, entirely agreeing with other material from Trans- -easpia (Askhabad, Bairam-Ali), Length of head and body 65 mm.(d) and 34 mm, (juv.). 6 to 9 superciliaries. The large supraocular shields completely or almost completely separated by a row of granules from the frontal and the postfrontal. Infranasal not reaching the rostral. 6 anterior and 3 posterior supralabials, 6 to 8infralabials. 5 or 6 chin-shields in the young, the first 3 or 4 forming a suture. 22 or 23 gular scales in a line between the suture of the chin-shields and the collar. 10 plates in the collar. 50 to 53 dorsal scales across the middle of the body. 30 trans- verse rows of ventral plates, the longest of which consists of 13 to 15 plates. 20/21 femoral pores. Supracaudal scales strongly keeled. ‘ 5. EREMIAS INTERMEDIA Stv. 3 typical specimens. Length of head and body 55 mm. (@ ), 37 and 38°5 mm. (juv.). In the 2 a granule between the prefrontals. 6 to 8 superciliaries. The large supraocular shields entirely separated by a row of granules from the frontal and the postfrontal*. 6+142 to 4 supralabials: 7 or 8 infralabials. 26 or 27 gular scales in a line between the suture of chin-shields. and the collar. 11 or 12 plates in the collar. 47 to 50 dorsal scales across the middle of the body. 29 or 30 transverse rows of ventral plates, the longest of them consisting of 16 to 18 plates. 13 or 14 femoral pores on each side. * J shall show in a more detailed publication that the subspecies transeaspica Nik., which,. according to the author, may be distinguished by this character, is ‘identical with the typical E. intermedia. REPTILES FROM THE RIVER TAJAN. 15- _ 6. Eremias (Mesauina) Gurrutata Licht. 1 Q. Length of head and body 49 mm. 5 superciliaries. Row of superciliary granules beginning behind the 7th super- ciliary only. Occipital as large as the ‘interparietal. 4 anterior and 3 posterior supralabials. 7 infralabials. 22 gular scales in a line between the suture of the chin-shields and the collar. Collar free, consisting of 9 plates. “40 dorsal scales across the middle of the body. 28 transverse rows of ventral plates. 10 femoral pores on each side. 7. EUMEGES SCHNEIDERI Daud. 1 spec. Length of head and body 109 mm.(¢) and 63 mm. (hgr.). 6+1 +3 supralabials in the ¢, 54+1-+2 only in the half- grown specimen, the middle one being fused with the following by forming a very large subocular. 8 infralabials. 4/5 or 5/8 nuchal plates. 25 or 26 dorsal tha ventral scales round the middle of the body. 68 scales in.a line between the suture of the @hin-shields and the anal plates. 8. EumeEcess scutatus Theob. 3 spec. Length of head and body 122 mm. (¢), 124 and 116 mm. (both 2). The head-shields offer many anomalies. In one @ the right supranasal is divided; the other @ has both prefrontals divided into two unequal parts, and two loreals on the left side. In the ¢ the parietals form a long suture behind the interparietal_ 4 to 6 superciliavies. 4 or 5+1+3 supra- labials, the last being very small. 7 infralabials. 3/4 or 4/4 nuchal plates. 21 dorsal and ventral scales round the middle of the body. 78 to 80 scales in a line between the suture of the ehin-shields and the anal plates. 9, MABUIA SEPTEMTENIATA Reuss. 2spec. Length of head and body 82 mm.(¢) and 90 mm. (¢). Supranasals meeting in a point (d) or separated (¢ ). Preefrontals separated from each other, the internasal forming a short suture with the frontal. 4 anterior and 2 posterior supra- labials. 8 infralabials. 34 or 35 dorsal and ventral scales round the middle of the body. 70 or 71 scales in a line between the suture of the chin-shields and the vent. 10. VIPERA LEBETINA L. 1 spec.* Length of head and body 520 mm. Tail incomplete. 10 supralabiis, 13/14 infralabials. 25 longitudinal rows of dcrsal scales. 121 ventral plates. * Tt was impossible to ascertain the sex of the snakes, the viscera having been removed. 16 Mk. L. A. LANTZ ON 11. Boga rrigoNnaruM Schneid. 2 specimens :— Length of head and body............... 510 480 mm. IDEMERAN @Fe UBM Cyoesnassane scoonacdoscosce LNG) 108, Number of supralabials ............... 8/9, the 3rd, 4th, and 5th entering Number of infralabials ............... 11/12 [the orbit. ie < DebilgeR} Memipoualshieldsieeyas pease ae 24+3 14343 Number of rows of dorsal scales...... 21 Number of ventral plates ............ 222 221 Number of pairs of infracaudals ... 86 84. 12. TAPHROMELOPON LINEOLATUM Brandt. 1 specimen. Length of head and body 790 mm. Length of tail 375 mm. 8 supralabials, the 4th and 5th entering the orbit. 11 infralabials. 2-+1/2+3 temporal shields. 12 rows of dorsal scales. 181 ventral plates. 121 paurs of infracaudals. 13. ZAMENIS RHODORHACHIS Jan. 2 specimens :— Length of head and body............... 715 6380 mm. TL SMERTN OP URL Gooscobonssaeaceso casconecs ASB 230; Number of supralabials ............... §, the 5th and 6th entering the Number of infralabials.................. 10 [ orbit. Temporal shields .................. 0.2. 2+5 to 8 irregular ones. Number of rows of dorsal scales... ... 19 Number of ventral plates............... 227 226 Number of pairs of infracaudals ... 121 117 These specimens have no red stripe along the back. 14, ZAMENIS DIADEMA Schleg. 4 specimens :— Length of head and body ............ 870 830 825 770 mm. JDEHVEXNN Oil TEM coononocpcsvceosducuocpsdes . US 190 215 = (140) ,, Number of supralahials ............... 11/12 12/18 10/11 12/13 Nember of infralabials ... ............ 11/18 12 13/14 ‘' 12 Number of rows of dorsal scales ... 27 29 27 27 Number of ventral plates ............ 225 244 217 234 Number of pairs of infracaudals ... 76 83 83 oa Behind the prefrontals a row of 3 accessory shields; in one specimen the median one is fused with the right inter- nasal. 3 (51) exceptionally 4 (aa) frenals. 2 preeoculars. Supralabials more or less separated from the loreals and entirely separated from the orbit by a row of small shields, the first of which may reach the postnasal; there are 2 or 3 shields between the supralabials and the loreals, 3 to 5 between the former and the orbit, and,sfollowing them, 2 or 3 postoculars. Temple covered with small irregular shields. REPTILES FROM THE RIVER TAJAN. M7 15. NaAvrrix TESSELLATA Laur. 3 specimens :— Length of head and body ............... 580 530 470 mm. DEMEAN OP TER GoScocatosseobosobondonooooncs LASS) 155 12S (Sete et ee Ly Number of supralabials .................. 8 Number of infralabials .................. 10/11 Number of preoculars . 4 2/3 2 Number of postoculars .................. 4 4 3 si eae ee ee Temporal shields .. ; soa 14+2+2 or 3 Number of rows of alone sores ties 19 Number of ventral plates ................ 176 170 176 Number of pairs of infracaudals ...... 70 73 69 In the specimen having 2 preeoculars and 3 postoculars the 4th and Sth supralabials enter the orbit. 16. Eryx miniaris Pall. 1 specimen. Length of head and body 355mm. Length of tail 30mm. Internasals separated by the point of the rostral. 4 scales between the postnasals. Round the eye a circle of 13 small shields, the lowest of them much enlarged and reaching the 6th supralabial, the two anterior ones a little enlarged (pree- oculars), the others (supraoculars and postoculars) about equal in size. Between the supraoculars 5 scales across the head. are Between the postnasals and the preoculars 8 (t+t+4) small loreal shields. 13 supralabials, the 3rd one being the highest. 20 infralabials, the first 3 or 4 enlarged, the others very small, with larger shields below them. EXPLANATION OF PLATE I. Fig. 1. Gymnodactylus microlepis, sp. u., 6, River Tajan. Vig. 2. G. fedtschenkoi Str., 6, Samarkand. Fig. 3. G. caspius Kichw., 9, River Tajan. Proc. Zoou. Soc.—1918, No. II. 2 Ue olka A ee ‘noltslacnnie’ ora ive, a k beset THE EXTERNAL CHARACTERS OF THE LEMURS. 19 4, On the External Characters of the Lemurs and of Tarsius. By R. 1. Pocock, F.R.S. [Received March 5, 1918; Read March 5, 1918.] (‘Text-figures 1-16.) TABLE OF CONTENTS. Page Imtroduchonewee et cern een te kee The Muzzle and the Rhinarium........................... 20 SINGH) and cain REE A Wat re ne ti AE KOO The Facial and Carpal Vibrissee ..................... 2 24 The Glands of the Fore Limb............................... 25 “Nave 18 leawnGlS PNG! WECLtes oon oesccacuodoodonconcsonnaccancenovess QU aires Su lin owas eeany ke i le NEG ’ Woe Alms ennel ies (CVAMNCIS 3,25. ccassenososecoe urononancean . 20) The External Genitalia of the Male ..................... 42 The External Genitalia of the Female ................... 47 General Conclusions and Systematic .................... 51 Introduction. The materials upon which this paper is based are mainly the lemuroid Primates which have died in the Zoological Gardens during the past ten years or so. Representatives of practically all the commonly imported menagerie species of the group have passed through my han¢s in that time, namely, species belonging to the genera Chiromys, Chirogaleus, Lemur, Galago, Perodicticus, and Mycticebus. For the loan of examples of Hemigalago and Tarsius 1 am indebted to Prof. Wood-Jones, the Society’s Prosector. I am also indebted to Mr. Oldtield Thomas and to Prof. J. P. Hill for the chance to examine other specimens of Tarsius. I have not, however, been able in all cases to see repre- sentatives of both sexes of the species; and of many admitted genera, notably Microcebus, Mixocebus, Lepilemur, and Loris, no specimens have come to hand. This applies also to the three genera of Indriside (Jndris, Propithecus, Lichanotus), which, like Tarsius, seem to be intolerant of captivity even in their own countries. The external characters of the Indviside, however, have been tolerably fully described and illustrated in Milne- Edwards and Grandidier’s great work on the Fauna of Mada- gascar. From this I have freely borrowed. Unfortunately no text accompanies the numerous plates on the various species of Lemuride# published in that work. Of other treatises dealing with the Lemurs on a comprehensive scale the most important is the paper by Mivart and Murie (Tr. Zool. Soe. vii. 1872), in which some of the external characters of a few diverse types are dealt with from the comparative point of view. ‘The rest of the bibliography consulted consists mostly of special memoirs on particular species, like Owen’s paper on Chiromys, HETOLUNGHSIHOE 20 MR. R. I. POCOCK ON THE EXTERNAL on Tarsius, Van der Hoeven’s on Perodicticus, Huxley’s on Arctocebus, Beddard’s on Hapalemur, and so forth. Many of the facts dealt with in the following pages are of course well known. Some characters, however, are here described, I believe, for the first time; and I trust that the collation of the facts and their comparative treatment may prove useful to future students of this group. In the matter of names [ have followed the conservative course of using Lemur for the species to which it has been by common consent assigned in all recent literature, although by the rules of nomenclature, it has no right to a place in the Primates at all, but belongs by Storr’s very definite selection to the Dermoptera, Galeopithecus volans being its type-species. Even if that selection be set aside, it appears to me that the “ indications” of the 10th edition of the ‘Systema’ show that the species known as Loris tardigradus is its type. This is clearly a case for the * Fiat’ Committee on Mammalian generic names; and it is my confidence that the Committee will see the wisdom of allowing Lemur catta to stand as the type of Lemur, that induces me to retain this generic name in its commonly accepted sense. Similarly I have employed Chiromys for the Aye-Aye (mada- gascariensis), although Daubentonia is the correct title for that species. The Fiat Committee, I believe, has these names now ‘under consideration. The Muzzle and the Rhinarium. The bestial aspect of the face of the Lemuroid as compared with the Pithecoid Primates is not due to the general elongation of the jaws. In this character the Lemurs are surpassed by Papio amongst the Pithecoids. It is due to two correlated features, namely, the retention of the primitive moist glandular rhinarium and the projection of the upper jaw supporting it beyond the level of the chin. The rhinarium is naked to a varying extent on its dorsal side and also beneath the nostrils laterally and in front. It is con- tinued downwards in front as a strip of grooved naked skin cleaving the upper lip to its inferior edge. At this point the lip is adherent to the gum covering Une premaxille, so that it is incapable of protrusion. Although the rhinarium is tolerably similar throughout the eroup, one or two variations may be pointed out. In the typical Masearene Lemurs, including Chirogaleus (text-fig. 1, A), the labial extension of the rhinarium is comparatively short and the later- ally extended infranarial portions shallow. In Perodicticus the infranarial portion is deeper ; but in Vyeticebws it is not so. In Galago crassicaudatus (text-fig. 1, B) the labial extension of the rhinarium is a little longer and thinner than in Chirogaleus and Lemur. In Hemigalago demidoffii it is remarkably long and gradually widens above where it passes into the infranarial portion CHARACTERS OF THE LEMURS AND TARSIUS. 21 ‘of the rhinarium ; but in the length and shape of the rhinarium G. senegalensis is intermediate between G. crassicaudatus and H. denvidoffi (text-figs. 1, C; 2, B). In Chiromys the vhinarium is not so prominent; the nostrils are longer, more slit-like, and separated in front by a narrower septum. The infranarial portion is very deep towards the middle line, reaching almost to the edge of the upper lip and making the labial extension of the rhinarium appear very short. In this genus also the frenum which ties the lip to the gum between the Text-figure 1. PRS EMIS AN Cay ayy, “ TANS Gy = (SAG SERS S Ms E . Rhinarium of Chirogaleus major. . Rhinarium of Galago crassicaudatus. Rhinarium of Hemigalago demidoffi. . Rhinarium of Chironys. . Nose of Tarsius. A B ¢: D iE points of insertion of the incisor teeth is somewhat longer than in ‘typical Lemurs, so that the lip is capable of being protruded to a slightly greater extent in the middle line. It is probable that the variations of the rhinarium and upper lip, like many of the structural characters in Chiromys, are correlated with the rodent dentition and peculiar method of feeding of this Lemur; but our knowledge of the function of the rhinarium is too imperfect to warrant more than a suggestion on this point (text-fig. 1, 1D), . 22 MR. R. I. POCOCK GN THE EXTERNAL I have not been able to examine in a fresh state the rhinarium of any species of Indrisidee. The muzzle of Z'arsius is very different from that of all Lemurs.. The only trace of the rhinarium, if such it can be called, that remains is a narrow rim of naked skin surrounding the nostrils, which are widely separated as in the Platyrrhine Pithecoid Primates. The nose scarcely projects at all, and the muzzle is squarely truncated and deep, and the upper jaw hardly overhangs the lower, so that in profile view the muzzle has a_ decidedly feline appearance, contrasting markedly with the generally canine appearance of that of the true Lemurs. The long upper lip is undivided and continuously hairy from side to side across the middle line, and its frenum is set higher above the incisor teeth, suggesting that the lip is susceptible of partial protrusion after the manner of the lip of the pithecoid Primates, but to a lesser degree (text-figs. 1, E; 2, A). The primitive muzzle of the Jemuroid Primates, with its rhinarium and adherent upper lip, is associated with the habit of drinking by means of lapping. The specialised muzzle of the pithecoid Primates with aborted rhinarium and_ protrusible upper lip is associated with the habit of drinking by means of suction. But Varsius, although more resembling the pithecoids in the structure of the muzzle, drinks, it is said, by the lapping method*. This fact is full of interest’in connection with the view, supported by other considerations, that Varsius links the Lemuroids and Pithecoids together. The Kar‘. In the species referred to Lemur the pinna of the ear is tolerably uniform in shape and structure. It is small and con- cealed to a greater or less extent by its own hairs and those of the surrounding area of the head. Its superior posterior edge is. not folded; but the anterior edge of the upper half forms a strong ridge overlapping the anteri ior end of the simple shelf-like supratragus (plica principalis) and descending below it and vanishing in the capsule of the pinna above and within the small lobate tragus. The antitragus is somewhat larger than the tragus, sommenmnes much lar ger (Lemur catta); and ahe deep: notch between them is appr oximately on a level with the external auditory meatus. The flap of the ear behind the antitragus is marked with a depression, the anterior and posterior margins of which are respectively the ridge running upwards from the anti- tragus and the adjoining postero-inferior edge of the pinna. The supratragus, forming the upper boundary of the capsule of * H. Cuming, P. Z.S. 1838, p. 67. Mr. Cuming also makes the interesting remark that when any object is put near a Tarsius, the animal “draws up the muscles of the face similar to a Monkey and show its.... teeth.” I have never seen Lemurs behave in this way. + Described in several types by Mivart and Murie, Tr. Zool. Soc. 1872. CHARACTERS OF THE LEMURS AND TARSIUS. 23 the pinna, is set comparatively high up, approximately halfway between the tragal notch and the upper edge of the pinna. In Chirogaleus (text-fig. 2, C) the ear is similar to that of Lemur, but the ear of Microcebus is provided with a much larger pinna which, judging from a living example, is ribbed above the capsule and capable of being folded as in the Galagos. In the latter, as is well known, the pinna is of great size. The portion of it just above the capsule is ribbed and grooved and susceptible of folding. The supratragus is more expanded and more flap-like Text-figure 2. Cc A. Head of Tarsius. B. Head of Hemigalayo demidoffi. C. Head of Chirogaleus major. 1). Head of Perodicticus. Figures drawn from spirit specimens. All X 3. than in Lemur and the pouch, probably the homologue of the bursa of the ear of the Carnivora, is set higher up than in the Lemurs. Wycticebus and Perodicticus have the pinna no larger relatively than in Lem, and it is simplified by the almost total suppression of the tragal and antitragal thickenings; but, as in Galago, the pouch is set high up and the supratragus is flap-like and valvular (text-fig. 2, D). As Mivart and Murie pointed out,. there is a small fold of the integument above the supratragus in Nycticebus, and a similar but better developed fold is developed 24 MR. R. I. POCOCK ON THE EXTERNAL in Arctocebus. Huxley cites the presence of this fold as one of the features distinguishing this genus from Perodicticus. Although the ear of Chiremys is relatively as large as in the Galagos, if is not ribbed and grooved above the capsule. The supratragus is a thickened ridge as in Lemur; but the tragus is not an angular projection as in that genus but a simple ridge, and the notch between it and the well-developed antitragus is comparatively deep and wide. Its lower rim, however, does not extend downwards so low as the external auditory meatus, the portion of the pinna just beyond this meatus being elevated as in Carnivora, Ruminants, and many other Mammals. The ear of Z'arsiws is similar in all essential details to that of . the Galagos, except that the supratragus and the antitragus are somewhat larger and more valvular (text- ime, A, Jah), The simplest type of ear in this group, and I suspect the most primitive, is that of Lemur and Chirogaleus, ears with a greatly expanded and ribbed pinna and valvular supratragus being derivative and specialised structures. According to this view the ear of Tarsius is the least primitive of all. It is gradationally linked with the ear of Chirogaleus by the ears of Galago and Microcebus. The Facial and Carpal Vibrisse. In the development of the facial vibrissze * the most generalised type I have examined is Chirogaleus major, where the mystacial, suplary: genal, and interramal tufts are all well developed (text-fig. 2, C). There is a single genal tuft on each side set low down behind the corner of the mouth. Most of the species referred to Lemur resemble Chirogaleus except that the inter- ramal tuft is absent; but in ZL. variegatus it is usually, if not always, retained, although of small size. ‘The full complement of tufts is present in Chiromys, but the vibrissee composing them are generally shorter than in the typical Lemurs, and in two cases the interramal tuft was reduced to a single vibrissa. In the Galagos (Galago crassicaudatus, G. senegalensis, and Hemigalago demidoffi) the vibrissee are poorly developed as com- pared with those of the typical Mascarene Lemurs, more par- ticularly Chirogaleus major, with which the Galagos were at one time associated. The interramal tuft appears to be invariably absent, and the genal tuft is set high up on the cheek a little below and behind the posterior angle of the eye (text-fig. 2, B). It resembles in position the upper genal tuft of the typical Carnivora, whereas in Chirogaleus and Lemur the genal tuft resembles in position the lower of the two tufts in that order. In Nyceticebus and Perodicticus the vibrissee are even less well developed than in the Galagos, the genal tuft being suppressed in the specimens examined (text-fig. 2, D). The genal and interramal tufts are also absent apparently in Tarsius, although * P.Z.S8. 1914, pp. 889-912. CHARACTERS OF THE LEMURS AND TARSIUS. 25 Burmeister figures some vibrissee in front of the ear. These do not, however, correspond in position to the genal tuft of the Galagos (text-fig. 2, A). The prevalence in most orders of Mammalia of the complement of tufts described above as occurring in Chirogaleus suggests that the absence of one or more of the tufts is a derivative and not a primitive feature. In this respect the Lorises, Pottos, and Tarsius are more specialised than the Mascarene Lemurs. The Carpal vibrisse in Lemurs have been studied by Beddard and Bland-Sutton. Confirming and extending their observations, I may add that I have found these tufts of tactile bristles in Chirogaleus major, Hapalemur griseus, and in examples of the following species of Lemur, namely, catia, variegatus, macaco, mongoz, coronatus, rufiventer, albifrons, and many of the species, subspecies or varieties grouped round the last. They are not always easy to detect in the thick fur, and sometimes appear to be wanting; but in such cases I suspect their absence is due to moulting or to artificial removal by rubbing. I have not found them in Ohiromys, Nycticebus, Perodicticus, or Tarsius; and, since Bland-Sutton also noticed their absence in Perodicticus, it may be inferred that their absence is characteristic of the Asiatic and African lemuroids*. ‘The prevalence of these vibrisse in many orders of Mammals suggests that they are a primitive Metatherian and Kutherian character, a suggestion which involves the conclusion that their absence in the above-mentioned Lemuroid genera is due to suppression and is a derivative feature. The Glands of the Fore Limb. In Lemur catta, but in no other species referred to the genus Lemur, there is a peculiar gland on the fore-leg, which was figured and described by Biand-Sutton + and also figured by Milne-Kdwards and Grandidier. A strip of black naked skin extends from the palm of the hand over the wrist up the distal third of the corresponding surface of the fore-leg. It ends proximally in a smooth elliptical area, which is present even in the newly-born young (text-fig. 3, A). In adult males the elliptical area is raised into a swollen cushion-like pad composed of white tissue, fatty in appearance and consistency and covered with black skin. On the ulnar side of the pad a large, erect, solid horny excrescence is developed (text-fig. 3, B). This varies in size apparently with age; its apex is sometimes bifid, but generally simple, and it is sometimes present on one limb and * J have failed to detect the carpal vibrissze on dried skins of Indris and Propi- thecus; and in both these genera the interramal tuft appears to be absent. Also in the one skin of Indris available for examination the genal tufts are wanting, whereas in a skin of Propithecus diadema these tutts are well developed and set low down on the cheek as in Lemuride. + Proc. Zool. Soc. 1887, pp. 369-372. In 1863 Gray pointed out the presence of this structure in Z. catta and its absence in other species. 26 MR. R. I. POCOCK ON THE EXTERNAL absent on the other. In females the excrescence is generally absent or quite small. Only in rare cases of probably aged individuals is it comparable in size to that of the males; and the elliptical area is generally flat in the females. Text-figure 3. A. Fore-arm of Lemur catta, newly born, showing the extension of the naked skin from the palm of the hand and the elliptical glandular area above the: wrist. B. Section through the glandular area and the horny spur of the fore-arm of an adult male Lem catta. C. Superficial view of the shoulder-gland of an adult male Lemur catta. D. Vertical longitudinal section through the same. E. Vertical transverse section through the same. F. Section through the shoulder-gland of adult female Lemur catta. According to Bland-Sutton the ducts of numerous sweat-glands. open upon the surface of the skin of the elliptical area. Secretion, no doubt, exudes through the pores; but I have never succeeded in squeezing any visible secretion to the surface by pressure. The only use I have seen the Lemur make of this structure is. to apply it to the tail by drawing simultaneously the applied wrists along that organ from near the base to the point. Possibly by this means the secretion is wiped on the long hairs. CHARACTERS OF THE LEMURS AND TARSIUS. 27 to scent them. But so far as my observations go, this action is. restricted to the male when stimulated to anger at the time of rut. Also in Lemur catta, but in no other species referred to the genus, there is a large gland in the male on the inner side of the upper arm near the top of the biceps muscle just below the shoulder (text-fig. 3, C). It is a circular or elliptical mound-like: elevation covered with short hair, except in the centre of the summit where there is a small naked area carrying the orifice of the gland which is usually shaped like a strongly curved crescent. In section the gland is seen to be composed of a thick-walled sac, the cavity of which is subdivided by ridges and outgrowths. of the walls, making, in a sense, a multilocular gland. It is the partial blocking of the rounded orifice of the gland by one of these outgrowths that gives the orifice its erescentic shape. The cavity of the gland is filled with strong-smelling brown sticky secretion which under pressure can be squeezed, like a worm, from the orifice (text-fig. 3, D, E). In the female this gland is not always developed, and when present it consists of a small elevation covered with normally long hair and having no cavity or trace of orifice (text-fig. 3, F). The suggestion that these glands are modified mf&immary glands is, | think, erroneous. At all events they coexist with the normal pectoral mammary glands. It is interesting to recall that Hapalemur also has a similar gland on the shoulder and a somewhat similar gland above the wrist. I have, however, seen these only on dried skins, and have nothing to add to the descriptions published by Beddard * and Bland-Sutton 7 But there are two points worth attention arising out of the facts just mentioned. Despite the development of these glands in Lemur catta and Hapalemur griseus, and in no other species, these two Lemurs do not appear to be nearly related. Judging from cranial and dental characters, the relationship of Hapalemur griseus is with Prolemur simus, and of Lemur catta with the other species usually assigned to the genus Lemur. The second point is the coexistence in two otherwise dissimilar genera of two sets of glands, one below the shoulder, the other above the wrist. This raises the very important question of possible correlation in development between two or more struc- tures, a question which opens a very wide field for research in zoology. The Hands and Feet. In the species of Lemur the digits of the hand are longish and slender, and free from webbing to approximately the same extent asin Man. The pollex is the shortest of the series and is sepa- rated by a wide space from the second, the base of which it * Proc. Zool. Soc. 1884, p. 393; and 1891, p. 450. + Proc. Zool. Soc. 1887, p. 369. 28 MR. R. I. POCOCK ON THE EXTERNAL slightly overlaps when laid forwards. It can be extended at right angles to the long axis of the palm, but is not truly opposable since the large composite palmar pad—-the “ ball” of the thumb— at its base is almost stationary. ~The succession of the digits in length is 4, 3,5, 2, but the fourth only exceeds the third slightly, and the second and fifth are approximately equal. The palm is longish, longer than wide, and passes proximally beyond the base of the pollex. Of the four interdigital pads, the first or pollical is confluent with the inner proximal (thenar), constituting the “ball” of the thunb. The remaining three interdigitals form a transverse trilobed cushion-lke pad. Behind the fourth or external interdigital, the external portion of the palm is occupied Text-figure 4. A. Foot and B.:Hand of Lemur macaco; X 2. 1, 2, 3, 4, the intermediate pads; I, II, the proximal pads. by the elongated external proximal (hypothenar) pad, which is subdivided, the posterior expanded portion lying alongside the posterior portion of the “ball” of the pollex, from which it is separated by a groove (text-fig. 4, B). In its main features the hand only varies in minor particulars in the different species examined, namely, 4. catta, macaco, albi- JSrons, mongoz, variegatus, and coronatus, except that in L. varie- gatus the palm is a little wider as compared with its length. In the foot the hallux is of great length and thickness, is capable of being extended at right angles to the sole, and is opposable, the “ball” of the hallux, consisting mainly of the large, projecting first or hallucal interdigital pad, being movable CHARACTERS OF THE LEMURS AND TARSIUS. 29: and capable of being pressed against the second interdigital pad and the elongated external proximal pad, closing up the depression in the middle of the lower surface of the foot. For the rest, the digits and the pads of the foot resemble in a general way those. of the hand (text-fig. 4, A). A point to notice is that in Lemur catta the naked sole is extended proximally to the tip of the caleaneum or heel. In the other species the heel is covered with hair, the hairy area being about one-third the length of the naked area, or a little more. Text-figure 5. A. Hand and B. Foot of Chirogaleus major ; nat. sized C. Hand and D. Foot of Galago senegalensis; nat. size. In Chirogaleus major the hands and feet are substantially similar to those of Lemur, but the naked palmar and plantar surfaces are broader as compared with their length, and the individual pads are more sharply differentiated, and, judging by their papillary ridges, endowed with greater tactile sensibility. In the foot the hairy area of the heel is relatively longer, being 30 MR. R. I, POCOCK ON THE EXTERNAL about two-thirds the length of the naked portion. In the speci- men examined the third and fourth digits were approximately equal both on the hands and feet (text-fig. 5, A, B). The hands and feet of the Indriside, as figured and described by Milne-Edwards and Grandidier, show some interesting pecu- liarities suggesting more complete adaptation to arboreal life than in the Lemuride. In Propithecus the digits of the hand are hardly more webbed than in Lemur, but the palm is narrower, especially posteriorly, where the pollex arises. The pads appear to be very little differentiated, and the absence of the “ball” of the thumb indicates a feeble grip for that digit. In Lichanotus (Avahis) the ball of the thumb is better developed, but the palm of the hand is apparently longer than in Propithecus, the second ; Text-figure 6. A. Foot and B. Hand of Chiromys; X 3. ‘digit, which is very short, being widely separated from the pollex. The third, fourth, and fifth are Jong and united by narrow webbing approximately to the ends of the first phalanges. In Jndris also the hand is long and slender, with a wide space between the long weak pollex and the second digit. The latter, however, is not so short as in Lichanotus, and is united to the third, as the third is to the fourth and the fourth to the fifth, by integument permitting but slight divarication of these digits and increasing in appearance the elongation of the palm. In the feet there is less variation. The hallux is normally -elongated, but is slender from base to apex without the muscular «development seen in other Lemuroidea, and the digits are webbed CHARACTERS OF THE LEMURS AND TARSIUS. Jl approximately to the distal ends of the first phalanges. In Indris the interdigital webbing 1s somewhat deeper than in the others and extends to an equal distance along all the digits, but in Propithecus and Lichanotus it is deeper between the third and fourth than between the second and third and the fourth and fifth. Some of the peculiarities of the hand of Chirom ys, such as the presence of claws and the modification of the third digit, are well known (text-fig. 6, B). The palm is narrower than in the true Lemurs. The pollex is not truly opposable, but it is so long that when turned forwards it overlaps the palm, asin Man. All the other digits are long, even the second and fifth, which are sub- equal, exceeding the Jength of the palm. The third is v ery long and slender ; the metacar pal that supports it projects beyond the palm, a unique modification which confers exceptional mobility on the digit. Nevertheless this digit is shorter than the fourth, which is nearly twice as long as the palm. Although a shallow web joins these two digits at the base, the hand may be described as unwebbed. In correlation with the grasping capacity of the large claws, the digital pads are comparatively slightly expanded. The feet are less modified than the hands and conform to those of the Lemur-type, except that the digits are thinner, the hallux _is a little shorter and weaker, the second, third, fourth, and fifth are a little longer and armed with claws correlated with narrower pads. The heel is covered with hair as in all Lemurs except L. catta (text-fig. 6, A). In this genus the unique elongation of the metacarpal of the third. digit of the hand and the slenderness of the digit are adaptations to feeding. In Galago of the er assicaudatus and senegalensis types the hand is wider than in Chirogaleus and its pads still better differentiated and more prominent, especially the first, or pollical, intermediate. All the normal six pads are distinguishable. The internal proximal is a small pad situated near the base of the outer border of the thumb, and the external proximal is a rounded pad in contact with the internal intermediate and not extending back- wards to the wrist as in Chirdgalews and the true Teams. A wide space separates it from the internal proximal, which is also set nearer the wrist. Similar differences obtain in the feet, where all the six pads are clearly defined. In G. crassicaudatus, montewt and their allies the BORteE part of the naked portion of the foot, as Beddard pointed out, is covered with coarse close- set papillze, and the hairy area of the heel is longer than in Chirogaleus major, being about as long as the naked poe tion. In G. senegalensis it is Neonsider ably longer (text-figs. 5, C, D; UNIS) i Hemigalago the pads show some interesting differences from those of Galago. In the hand the six pads are even more sharply defined, and are arranged so as almost to encircle a large naked submedian area of wr inlled skin. The two proximal pads 32 MR. R. I. POCOCK ON THE EX'TERNAL are almost in contact in the middle line, the external being elon- gated and extending practically from the wrist up to the internal intermediate. Behind the two proximal pads there is a short Text-figure 7. A. Hand and B. Foot of Galago crassicaudatus. 1-4, the intermediate pads; I, II, the proximal pads. area of naked wrinkled skin. The pollex is longer and more prehensile than in Galago. The arrangement of pads on the foot is similar, but the two proximal pads are relatively much smaller than in the hand, and the internal is set farther from the CHARACTERS OF THE LEMURS AND TARSIUS. 30 hallucal intermediate and is widely separated from the external. In this genus there is no definite heel-like area behind the pads as in Galago, the skin round the proximal pads being merely soft and creased. The hairy area of the foot back to the tip of the caleaneum is nearly twice as long as the naked area (text- sa) val, 185). Text-figure 8. . A. Hand and B. Foot of Nycticebus; x 2. C. Hand and D. Foot of Perodicticus; X< 2. 1-4, the intermediate pads ; I, II, the proximal pads. The arrangement and distribution of the pads give a primitive stamp to the hands and feet of Hemigalago in the sense that they recall very forcibly the pad-development seen in the extremities of many Rodents, Insectivores, and Marsupials. The hand of Mycticebus and Perodicticus differs in some Proc. Zoou. Soc.—1$18, No. III. ; 3 34 MR. R. I. POCOCK ON THE EXTERNAL remarkable particulars from that of the other genera hitherto noticed. It is capable of being turned at right angles to the axis of the forearm. ‘Lhe palm is short and broad, and the powerful pollex can be set so far backwards that its long axis is practically in the same line as that of the palm and of the fourth and longest digit, thus giving the widest possible span to the extre- mity, and when the pollex is in this position the internal proximal pad, constituting the proximal portion of the “ball” of the thumb, lies nearly in a line behind the external proximal pad. The pollex, moreover, is Incomparably more strongly opposable than in any other genus of Lemuroid Primates, and surpasses even the thumb of Man in that respect. When brought into opposition, the composite ball of the thumb is pressed against the second intermediate pad and the external proximal pad. Except that the hallux is a little longer and stronger than the pollex, the feet conform to the hands in type. In all other genera of Primates the two extremities are dissimilar. As is well known, the second digit of the hand in Vyecticebus is dwarfed and in Perodicticus is represented by an excrescence upon the second intermediate pad. For the rest the hand of Perodicticus is narrower with reference to its span, and the third and fifth digits are tied basally by a shallow web to the fourth, xo that the three cannot be so w idely separated as in WV, yovicebus. In the feet of both genera the heel is hairy and shorter than the naked part of the sole, the second digit is dwarfed, and the third and fifth are basally webbed to the fourth in Perodicticus, free in Vycticebus. The nails on both extremities are larger in the former than in the latter genus (text-fig. 8, A, B, C, D). The published descriptions of the extr emities of Arctocebus suggest that they differ from those of Perodicticus in having the third, fourth, and fifth digits more completely webbed (see P. 2.8. 1864, pp. 316- 317, 319-- 320). Huxley, however, states that the calcaneal tuberosity of the foot is naked and separated from the padded portion by a narrow band of hair. But since the heel is without exception covered with hair in all the remaining species of arboreal * lemuroid Primates, I suspect that the nakedness mentioned by Huxley was due to artificial rubbing in the specimen he examined. It is not uncommon for the hair to be worn off the heels in captive examples of common lemurs (Z. albifrons, etc.). In the distinctness and separation of the pads and their encircling arrangement round a central palmar area, the hand of Tarsius vecalls that of Hemigalago; but there ave certain differ- ences. The hand and fingers of Varsius are relatively longer, the pollex is smaller, closer to the second digit and not opposable, the third digit is the longest of the series, slightly surpassing the second and fourth, which are subequal. The first, ox pollical, * Lemur catta, which has the heels naked along the middle line, lives in rocky hills. CHARACTERS OF THE LEMURS AND TARSIUS. © 35 intermediate pad is small and rounded, smaller than and in con- tact with the internal proximal, which is elongated and surpasses the external proximal in length. The second intermediate pad is markedly larger than the others of that series. Finally, the nails ave sharply pointed, compressed and convex from base to tip, simulating claws, nearly the distal half being free from the pad though normally resting upon it (text-fig. 9, C). Text-figure 9, A. Hand and B. Foot of Hemigalago demidoffi ; nat. size. C. Hand and D. Foot of Tarsius; nat. size. 1-4, intermediate pads ; I-II, proximal pads. In the feet the hairy area back to the heel is shorter than in Hemigalago, and the naked padded area and digits longer. The plantar pads are peculiar. The hallucal, or first, intermediate is large and prominent, and is fused to the internal ee to 36 MR. R. I. POCOCK ON THE EXTERNAL form a single long pad which sometimes fuses proximally i in the middle line with the external proximal, which is itself united to the external intermediate, forming a long pad extending along the outer edge of the sole of the foot. The second and third intermediates are united to form a single large elongated pad, broad distally, narrowed proximally, where it terminates in the middle of the membranous area of the sole. Of digits two to five the fourth is the longest as in Lemuroid Primates; but the third has an erect claw like the second—a characteristic not found in any Lemuroids, but probably primitive and forcibly recalling the corresponding “ syndactyle” digits of many Marsupials (text- 1a, 8), ID). The Sublingua. There are one or two points to be recorded in connection with the swblingua, an organ which is especially well developed in the Lemuroid Primates. Typically it is a thin flat fibrous plate, lyrate or leaf-like in form with free apex and free lateral margins. It covers a considerable area of the lower surface of the tongue, the frenum of which arises from an angular notch in the middle of its posterior border. The pointed or truncated apex is ser- rated or denticulated to a varying extent, and the underside is strengthened by a fine median longitudinal ridge, with frequently a smaller ridge close to it on each side, making three in all. Beneath the sublingua the floor of the mouth is provided in front with a pair of small soft flaps, the frenal lamelle, arising at the bottom of the lingual frenum and continued backwards to a varying extent as a free narrow edge towards the base of the tongue. A similar and homologous structure is prcsent in some other Mammals—e. g., Canis, Pteropus, where, as in the Primates, it overlies the orifices of the sublingual and submaxillary salivary glands. In the species usually referred to Lemur the sublingua ex- hibits certain structual differences, which examination of a larger number of individuals than I have seen may show to have systematic value. For instance, in JL. variegatus there are three comparatively strong denticles at the tip and three corre- spondingly strong keels below. In other species the tip is rather serrulate and the keels weaker. On the other hand, I have noticed differences in the shape of the sublingua within specific limits. In a male of LZ. coronatus, for example, it was lyrate with bulging postero-lateral margins; in a female it was evenly attenuated, the two margins gradually converging from near the base to the tip. In the male again the frenal lamellae formed together a broad semicircular flap ; ; in the female they were narrower, forming a nearly parallel-sided flap. In a male specimen of L. albifrons albifrons and in a female of L. a. nigrifrons the frenal lamelle were of the same shape as in the male ZL. coro- matus; but inexamples of L. variegatus, macaco, catta, and mongoz the lamelle were narrow and resembled more or less closely those CHARACTERS OF THE LEMURS AND TARSIUS. Bi of the female LZ. coronatus mentioned above (text-fig. 10, A—D, G). In Chirogaleus major the narrowed sublingua is apically serrulate and the frenal lamelle are narrow as in most Lemurs. The sublingua of Hapalemur was briefly described by Beddard. Text-figure 10. . Lower side of tongue of Lemur coronatus. . Sublingua of another specimen of the same species raised from the frenal lamellee. . Lower side of distal end of tongue of Lemur variegatus with the tip of the sublingua showing beyond the frenal lamellz. . Lower side of tongue of the same without the frenal lamellz. . Lower side of tongue of Galago crassicaudatus. . The same of Nycticebus with supplementary frenal lamelle. . Side view of tongue of Lemur coronatus. . The same of Galago crassicaudatus. Q b> DQ sl., sublingua ; fJ., frenal lamelle. 38 MR. R. I. POCOCK ON THE EXTERNAL The sublingua is also present, as Milne-Edwards and Grandidier have shown, in the Indriside.” It has a single median inferior crest and three apical denticles. In Propithecus it hardly differs in form from that of the Lemuride, being broad at the base posteriorly, nearly parallel-sided, and attenuated at the apex. In /ndris its lateral edges are rather strongly convex, the base being narrowed like the apex. In Lichanotus it is very short, its free lateral edge being apparently only about half as long relatively as in Propithecus and Indris. In Galago, Nycticebus, and Perodicticus the sublingua is broader than in the Lemuride, especially at the apex, which is almost truncated and armed with many denticles—z. e. 9 in a Galago monterri—and its attachment to the tongue in the middle line is set farther back so that a greater extent of its apex is free. I also noticed 9 denticles at the tip in a specimen of Perodicticus theanus. But in both Perodicticus and Galago these denticles form a continuous series, whereas in an example of Vycticebus, with 7 denticles, the outer on each side was larger than the rest and separated from them (text-fig. 10, E, F, H). In Chiromys the sublingua is of a different type. It has a free lateral margin, but towards its abruptly attenuated tip it is closely adherent to the tongue. It is not denticulated, but ends in front in a firm, deflected hook which is the anterior termi- nation of a thick median keel or ridge, itself carrying two or three teeth, and traversing the whole of the underside of the sublingua back to the upper end of the lingual frenum. Just in front of the point there is on each side of the sublingua a.small, probably glandular pouch, like a watch-pocket, with its orifice looking forwards. The frenal lamelle are present and narrow; but I could not be sure of their exact form. In the example of this genus I examined the sublingua is less cordate and the tongue less rounded than depicted by Owen, who, moreover, did not mention the small teeth on the carina or the pocket-like glands near the base of the sublingua (text-fig. 11, A, B). The sublingua of Varsiws, described and figured by Burmeister, is different from that of Lemurs. It is not so well developed, is softer in consistency. and is defined from the tongue laterally by a groove. In the middle it is provided with a rod-like thickening which has a knob-like expansion at the apex. This rod, corre- sponding to the median carina of the sublingua seen in Chiromys and other Lemurs, was compared to the lytta of the tongue of Canis by Burmeister. But the bifurcation of this rod and some other structures at the tip of the sublingua described by that author I was unable to detect in the single example of the tongue of Tarsius I examined. In this specimen the frenal lamelle consist of a pair of longish slender processes, each tipped with a few small projections. At the proximal end of these processes on the outer side the edge expands abruptly to form a flap with a lobulate margin which extends far backwards along the sides of the tongue. Burmeister described the frenal lamelle as the CHARACYERS OF THE LEMURS AND TARSIUS. 39 ‘‘Unterzunge.” His figure represents this structure as an undivided semielliptical lamina with evenly denticulated margin. This does not agree with my observations (text-fig. 11, C—E). It has been suggested that the sublingua of the Lemurs acts as ~a tooth-brush to clean the porrect, close-set, and comb-like series of anterior mandibular teeth. Lemurs certainly use these teeth to comb their own fur and that of their companions. I have never seen them employ these teeth for any other purpose, and Text-figure 11. . Side view of the tongue of Chiromys. . Lower view of the same. . Lower view of the tongue of Tarsius raised from the floor of the mouth. . The same extracted with the frenal lamelle and the fringe attached. . Side view of the tongue of Tarsiws, showing the comparatively slight * differentiation of the sublingua and the well-developed frenal lamelle with backwardly extending lobulated fringe. soon PS since there is frequently a rapid movement of the tongue after the combing action, I do not doubt that the suggestion as to the function of the sublingua is correct; and the suggestion is strengthened by the structure of the sublingua in Chiromys, where the median keel ends in a firm hook well adapted to all appearance for removing particles lodged between the two rodent incisor teeth of the lower jaw. . 40 MR. R. I. POCOCK ON THE EXTERNAL In connection with the fur-combing use of the pectiniform mandibular teeth in the true Lemurs, it must be remembered that the spatulate finger-tips and short nails of these animals deprive the digits of the scratching power they possess in ordinary mammals with narrow finger-tips and comparatively long claws or nails. Only one digit in the Lemurs is functional as a scratcher, namely, the second of the hind-foot, which is short with small terminal pad and long semi-erect claw. Thus is established a most interesting correlation of characters in the Lemurs :—namely, the uselessness of the fingers for scratching the fur, the modification of the anterior mandibular teeth to sub- serve that end, and the differentiation of the sublingua to keep these teeth clean from seurf and hair. Now in Z'arsius the lower mandibular teeth are not modified to form a comb. Possibly they are employed for cleaning the coat, but their structure makes them less lable to be clogged, and at the same time less efficient instruments for the purpose than the corresponding teeth of the typical Lemurs. Possibly, perhaps probably, for these reasons, the sublingua is less differentiated and two of the digits of the hind-foot, the second and third, are set apart as scratchers and are capable of acting in unison, almost like the corresponding united digits of the syndactylous Marsupials. The sublingua of Chiromys probably serves mainly the purpose of keeping the gnawing-teeth free from woody fibre; and, for anything I know to the contrary, it may also cleanse them of hair and scurf. But I am not aware whether these teeth are used as a comb or not. At all events, in the case of this genus it is interesting to note that the absence of the typical lemurine dental comb is accompanied by well-developed claws and by fur of a very different texture from that of ordinary Lemurs, since it consists of a light underwool covered by long coarse hairs. Possibly the fisefulness of the claws in combing this fur has been one of the principal guiding factors in their evolution from nails. The Anus and its Glands. In all the Lemuroids examined, with one exception, the anus is Situated in the normal, position below the joint of the tail so that the base of that organ, when depressed, closes over it. But in Chirogaleus major it is placed below, or on the distal side of the joint of the tail, so that when that organ is raised the anus is carried up on its base (text-fig. 16, A). Normally in this group, that 1s to say in WVycticebus, Perodic- ticus, Galago, Chiromys, the Indriside appar ently, and in Lemar catia, variegatus, and coronatus, the per ineal and circumana] areas are covered with hair; but in LZ. macaco, LZ. albifrons, and the various forms such as nigrifrons, rufus, fulvus, cinereiceps, asso- ciated with albifrons, these regions are covered in both sexes with nearly naked, folded, wrinkled, and glandular skin, and similar naked skin extends for an inch or so along the root of CHARACTERS OF THE LEMURS AND TARSIUS. 4] _ the tail (text-figs. 12, A; 15, BE). In other species referred to this genus, i.e. L. mongoz and L. rubriventer, the glandular area is much less differentiated, the skin being more closely covered with fine, short hair and less distinctly folded and wrinkled. Text-figure 12. ANS SA We Was , O Z Yr Ge : 1 “a AN C A. Anal and genital area of male Lemur albifrons, showing the nearly naked glandular skin stretching from the root of the tail to the scrotum. B. The same of Lemur mongoz, showing the hairy but partially wrinkled skin round the anus. CQ. The same of female Lemur mongoz, showing the absence of wrinkled skin round the anus, the long grooved clitoris (cl.), and the orifice of the urethra (u.) below that of the vagina (v.). D. The same of male Lemur catta, showing the hairy unwrinkled skin round the anus and the naked scrotum. 42 MR. R. I. POCOCK ON THE EXTERNAL The only example of ZL. rubriventer examined, namely a female, had the skin of the circumanal area distinctly but not strongly ~ wrinkled. On the other hand, some females of Z. mongoz show no sign of wrinkling, others show traces of it, and in some males the wrinkling is rather strongly pronounced. A complete gradation therefore in the development of the glandular area can be traced from ZL. coronatus through L. mongoz to L. macaco and L. albifrons (text-fig. 12, A-C). The paired anal glands, so well known in some orders of Mammals, e. y. the Rodentia and Carnivora, appear to be absent in almost all Lemurs. The only genus in which I have found a trace of them is Chiromys, where they are represented by a pair of small, shallow invaginations, one on each side of the anal orifice. The External Genitalia of the Male. According to Milne-Edwards and Grandidier each of the three genera of Indrisidze may be characterised by the structure of the penis and baculum. The penis appears to be short, subcylin- drical, and apically truncated, and the baculum is distally biramous in all cases. ; In Lichanotus the epithelium is striated, and there are on each side of the organ near the middle of its length two strong recurved spines set one above the other. The baculum is greatly expanded at its proximal end and gradually narrows from the thickening to the middle of its length. From that point the two sides diverge gradually to the apices of the two branches, which themselves diverge evenly at about an angle of sixty degrees, each branch being rather less than one-third of the length of the whole bone. In /ndris the epithelium of the penis is irregularly reticulated, and on each side of the organ there is a patch of rather small spines set in three irregularly vertical rows which extend also to the underside. The baculum differs from that of Jichanotus in being thicker in the middle of its length, without any proximal (or basal) expansion, and in having the two branches much less divergent and a little longer, each slightly exceeding one-third the length of the entire bone (text-fig. 14, C). In Propithecus the epithelium of the penis is grooved and beset with minute spicules. The baculum differs from that of Zndris in having the branches very long, each being more than half the length of the entire bone, longer, that is to say, than the stalk instead of shorter as in /ndris and Lichanotus. The penis of Chirogaleus major (text-fig. 13, I, K, L) is rather short and broad, nearly parallel-sided, with an ovate extremity giving it a somewhat linguiform appearance from the lower or upper view. It is longitudinally grooved and closely punctured, the punctures possibly marking the position of minute spicules CHARACTERS OF THE LEMURS AND TARSIUS. 43 rubbed off. The orifice of the urethra is situated above the pad covering the tip of the baculum, a character in which the penis Text-figure 13. WV, mn les) Zim A. Penis of Galago crassicaudatus from below with the frill folded over the tip of the glans. B. Tip of the glans of the same with the frill spread. }. End of the penis of the same from the side with the tip protruding from the frill. D. Penis of Galago senegalensis from below. E. Tip of the glans of the same showing the absence of the frill. ¥. Penis of Nycticebus from the side. G. Tip of the glans of the same to compare with B and E. H. The same of Perodicticus. I. Penis of Chirogaleus major from below. K. Tip of penis of the same showing the orifice of the urethra above the tip of the baculum. L. Penis of the same from the side with a probe passed dowa the urethra. M. End of penis of Lemur macaco from below. N. The same from above. O. Penis of Lemur albifrons from the side. P. Tip of penis of the same. 44 MR. R. I. POCOCK ON THE EXTERNAL differs from that of all the Lemuroid Primates examined by me. Above the orifice there is a transverse glandular depression overlapped by a thick flap of epithelium. A somewhat similar crescentic flap half encircles the bacular pad laterally and below. The baculum (text-fig. 14, A, B) itself is a little longer than that of an adult example of Lemur albifrons more than twice the size of Chirogaleus major. Seen from the side the baculum shows a slight sinuous curvature, the distal half being depressed. Seen from above or below, the main part of the shaft is straight and subcylindrical, but its apical fourth is divided into two curved branches, a right and left, which diverge at first, then converge so as almost to meet apically in the middle line, circumscribing an ovate space. The urethra, which runs along the underside of the main portion of the baculum, passes through this space at the point of bifurcation of the baculum. Hence it comes about that the orifice of the urethra lies above the pad which covers the juxtaposed tips of the two branches, In being distally biramous the baculum of Chirogaleus resembles that of the Indrisine Lemurs, a point of great interest. It is most like that of Lichanotus, but has the base less expanded and the branches curved and convergent apically instead of widely divaricated. According to Beddard Hapalemur also has a bifid baculum. I do not know the course of the urethra with regard to the baculum in the Indriside, nor is Beddard quite clear on this point in his description of the penis of Hapalemur, but since he states that the urethra opens at the posterior end of a groove marking on the glans penis the forking of the baculum, it may be inferred that the orifice of the urethra is beneath the tip of the baculum as in typical Lemurs and not above it as in Chirogaleus. On one of the plates of his unfinished work Milne-Edwards illustrates the male genitalia of a Lemur which, although un- named in the legend, is clearly shown to be Z. catta by the naked» scrotum. Four bacula are figured on the same plate. They may have been taken from. specimens representing four distinct species or from four examples of ZL. catia. If the latter, the figures attest a certain amount of individual variation in this bone, particularly in width at the base and expansion and curvature at the tip. There the matter must rest. In the species I have examined, namely L. catta, macaco, - albifrons, and coronata, there is very little variation in the penis and baculum. The penis (text-fig. 13, M-P) is subcylindrical and armed in the middle of its length with many reversed spines which are mostly of smal] size; two or more pairs, however, on each side are much larger than the others, but these large spikes are not always either symmetrically placed or numerically iden- tical on the two sides. The orifice of the urethra is terminal and opens just beneath the tip of the baculum. The baculum is a comparatively short and slender rod with a larger proximal and CHARACTERS OF THE LEMURS AND TARSIUS. 45 a smaller, sometimes incipiently bilobed distal expansion. As compared with the size of the animals, the baculum in the species referred to Lemur is smaller than in any other genus (text-fig. 14, H). In Galago senegalensis the penis is long (text-fig. 13, D, E). Its narrow and cylindrical, proximal portion gradually expands distally to a considerable extent, and its terminal portion is attenuated. The orifice of the urethra, opening beneath and behind the hardened rounded pad covering the tip of the baculum, is provided with a small inferior and two small lateral labia. Except at the distal and proximal ends the epithelium of the penis is thickly beset with comparatively coarse reversed spines Text-figure 14. a ee Gari, Al aishagwce ae (co f H A. Baculum of Chirogaleus major from the side, the line indicating the course of the urethra. BB. The same from above showing the apical bifureation. C. Baculum of Indris trom above (copied from Milne-Edwards). ID. The same of Galago senegalensis from the side. E. The same of Galago crassicaudatus. F. The same of Nycticebus. G. The same of Perodicticus. H. The same of Lemur albifrons. I. The same of Chiromys. (All the figures twice nat. size.) approximately equal in size. The baculum (text-fig. 14, D) is long and slender, being actually nearly twice as long as that of an adult male Lemur albifrons. It is practically straight and gradually attenuated from its broad base, but there is a slight sinuosity in its distal third and a slight and gradual thickening at the apex which is blunt. 46 MR. R. I. POCOCK ON 'THE EXTERNAL In Galago crassicaudatus and monteiri (text-fig. 13, A-C) the penis differs considerably from that of G. senegalensis. It is clavate in form, being gradually incrassate from the base to the blunted tip. The orifice is just below the apex of the baculum, and the two are encircled by a frill of grooved, wrinkled epithe- lium, forming a sort of secondary prepuce, which is attached by a frenuin to the lower lip of the orifice and encloses a glandular space. The spines covering the penis are bidentate or tridentate, and much smaller than in G. senegalensis. The baculum (text- fig. 14, K), although actually longer than in G. senegalensis, is approximately the same shape and relatively about the same size. In Vycticebus the penis (text-fig. 13, F, G) is much shorter than in Galago and smooth and of tolerably even thickness through- out. The callous pad at the tip of the baculum is large, rounded and prominent, and overhangs the orifice of the urethra, which lies in a glandular space bounded laterally and below by a pair of labia practically as in G. senegalensis. The baculum (text- fig. 14, F) is a nearly straight rod, only about two-thirds the length of that of G. senegalensis, although the animal itself is much bigger. In Perodicticus the penis (text-fig. 13, Hl) i is short and smooth and like that of Vycticebus except that, the tip of the baculum and the orifice of the urethra are surrounded by a complete hood or frill of wrinkled epithelium enclosing a circular glandular space. The baculum (text-fig. 14, G) in the specimen examined is shorter than that of the éxample of Vycticebus, but decidedly thicker at the base inferiorly and with its upper edge a little more sinuous. According to Huxley's description (P. Z.S. 1864, p. 334) the extremity of the glans penis in Arctocebus closely resembles that of Perodicticus except that the encircling hood is bifid in the middle line below. He states, however, that the baculum is :75 of an inch in length, about twice as long, that is to say, as in my example of Perodicticus, although, judging from the dimensions of the limbs, his animal was considerably the smaller of the two. In Chiromys the penis is rugulose, wrinkled, and very slightly narrowed distally for three-fourths of its length, then somewhat abruptly attenuated to the apex, where the upturned tip of the baculum terminates; but just below this point there is a little soft, curved, subcylindrical process upon which it seems probable the orifice of the urethra opens. When the prepuce is reflected to its fullest extent, the basal fourth of the exposed portion of the penis is seen to be provided with five probably glandular, longi- tudinal grooves, one in the middle line above a two on each side, one above the other, the ventral middle line being occupied by the frenum. The baculum (text-fig. 14, I) is tolerably stout and longer than in any genus of Lemuroid known to me. Allowing for its curvature, it is as long relatively as in Galago er assicuudatus. When seen from the side it is markedly sinuous, its upper edge CHARACTERS OF THE LEMURS AND TARBSIUS. ~ 47 being concave close to the base, then convex, then strongly con- cave owing to the upeurling of the distal fourth of its length. The ventral side is curved in correspondence. No other Lemuroid known to me has a strongly upcurled tip to this bone. In connection with the scrotum there is one fact to be re- corded. In Lemur catta this sac is always naked (text-fig. 12, D). In all other species of Lemuroid Primates it is clothed with hair normally (text-figs. 12, A, B; 16, A). Occasionally the postero- inferior portion is naked, as J have noticed in one or two specimens of Galago; but I have no doubt that in these cases the absence of the hair was due to rubbing. The External Genitalia of the Female. In the standard text-books of Mammals published even as recently as Max Webew’s in 1904, it is stated that the urethra traverses the clitoris in the Lemuroidea. This is not true of any Madagascar Lemur I have examined, and applies only to the Asiatic and African forms. In the Madagascar species \the urinary orifice opens at a varying distance between the vaginal aperture and the apex of the clitoris, generally much closer to that orifice and only in one case, Lemur catta, a little nearer the tip of the clitoris. Milne-Edwards and Grandidier have shown that the clitoris varies considerably in form in the three genera of Indriside. In Lichanotus (Avahis) it is long, pendulous, and narrow, and parallel-sided invits distal two-thirds, but expanding proximally towards the orifice of the vulva. From the orifice of the urethra, situated a little below the vulva, a groove extends towards the tip of the clitoris, and at the extreme tip of the latter is placed the aperture of a glandular depression. In Propithecus the clitoris is much shorter and thicker, with a broadly rounded distal end carrying a glandular orifice. The aperture of the urethra les approximately midway between the orifice of this gland below and of the vagina above. In Jndris the distal end of the clitoris is gradually and widely expanded laterally and extended considerably beyond the orifice of the gland, but the orifice of the urethra is situated even nearer to the vulva than in Lichanotus. In the species usually referred to the genus Lemur there is considerable variation in the structure of the genital area of the female. In Lemur varius the clitoris is a short, thick, fleshy excrescence with a blunt apex and somewhat cordate in shape, rising from the centre of a tolerably large area of naked skin. Its free posterior surface 1s marked by a median groove or rima defined laterally by a pair of thick labia. When the Jatter are separated the urinary channel, a gutter with thin elevated margins, is displayed. In a mated female this gutter is seen to lead from 48 *, MR. R. I. POCOCK ON THE EXTERNAL Text-figure 15. A. Anal and genital area of female Lem catta, showing the thick clitoris protruding between the labia of the vuiva. B. The same of female Lemur variegatus, showing the short cordate vulva arising from a naked area of skin. C. Vulva of the same enlarged, showing the lateral grooves and the orifices of the urethra and vagina covered by membrane (hymen) in the virgin female. T). Side view of the same vulva. EK. Anal and genital area of female Lemar albifrons, showing the circumanal elands and the long attenuated clitoris. F. The same of Lemur coronatus, showing the long clitoris and the absence of circumanal glands. ‘ G. Vulva of the same on larger scale, showing the supplementary labia beneath the orifice of the vagina. cl., clitoris ; w., orifice of urethra; v., orifice of vagina. ; . CHARACTERS OF THE LEMURS AND TARSIUS. 49 the orifice of the urethra, which is just below that of the vulva; but in a virgin female the two orifices are concealed by a flap of membrane (hymen), below the edge of which the open channel extends, narrowing in its course to the apex of the clitoris. The sides of the clitoris are marked by a couple of deep, probably glandular, grooves (text-fig. 15, B, C, D). In Lemur catta the clitoris is a thick elongated excrescence Text-figure 16. A. Anal and genital area of male Chirogaleus major, showing the position of the anus on the root of the tail. B. The same of female Hemigalago demidoffi, showing the long pendulous clitoris below the vulva. C. The same of female Galago crassicaudatus with the labia of the vulva spread open. PD. Vulva of the same with the labia closed. I. Vulva of the same from the side. F. Anal and genital area of female Tarsivs, showing the labia of the vulva partially spread open. G. The same from the side with the labia closed. el., clitoris; 7., labium of vulva; w., orifice of urethra; v., orifice of vagina. Proc. Zoou. Soc.—1918, No. IV. 4 50 MR. R. I. POCOCK ON THE EXTERNAL with the orifice of the vulva at its base and that of the urethra about one-third of the distance from the tip—much lower, that is to say, than in Z. varius. The urinary channel runs from the urethral orifice to the apex of the clitoris. The orifice of the vulva is bounded on each side by a pair of thick labia, which, when separated, diverge from above that orifice and inferiorly disappear in the area of naked integument from which the clitoris rises (text-fig. 15, A). In L. macaco, albifrons, fulvus, mongoz, rufiventer, and coro- natus, the clitoris is narrow, elongated, attenuated towards the apex, and arises from an area of naked or nearly naked skin. It is channelled to the apex from the orifice of the urethra, which opens a short distance below that of the vagina. It varies to a certain extent in length within specific limits, e.g. Z. albifrons, and is rather exceptionally long, less attenuated and narrower at the base in Z. coronatus than in the others. Moreover, in the single example of this species examined, two pairs of elongated laminz, constituting labia, diverged obliquely just below the orifice of the vagina (text-figs. 12, C; 15, E, F, G). In the Asiatic Lemuvoids the clitoris differs from that of the Madagascar forms in being traversed by the urethra which opens at its tip. In Galago crassicaudatus the clitoris is elongated. thick from before backwards in profile view, and parallel-sided and com- pressed from the posterior aspect : at its tip there is a depression, probably glandular, almost encircling the urethral orifice, and comparable to the similarly situated gland in the Indriside. The vulva consists of two turgid labia, of which the opposed surfaces are provided with several small fine lamine, running from the edges of the labia inwards towards the orifice of the vagina (text-fig. 16, C. D, E). In Hemigalago the clitoris is relatively much longer and thinner than in G. crassicaudata. The distal portion appears to be strengthened by a baculum and the tip is provided with a glandular depression encircling the end of the bone. The two labia at the sides of the orifice of the vagina are relatively smaller than in G. crassicaudatus (text-fig. 16, B). In Vycticebus the clitoris is short and thick, resembling the prepuce of a penis. There is a glandular depression at the tip. The orifice of the vagina is a wide transverse rima just at the base of the clitoris. The general appearance of the external genitalia is very different from that of Galago and Hemigalago. Possibly the specimen examined was a virgin female. The female external genitalia of Zarsiws are unlike those of the Asiatic and Masearene Lemurs, but in the single example examined recall rather those of the Old World pithecoid Primates. The vulva is a laterally compressed, elongated excrescence, with- out pendulous apex. The rima is short and bounded by a pair of labia concealing the small clitoris and the orifices of the CHARACTERS OF THE LEMURS AND TARSIUS, 51 arethra and vagina, which are comparatively close together. It is significant that the vulva of this genus as a whole is less like the vulva of the Galagos than that of the true Lemurs. It ‘approaches most nearly the vulva of LZ. varius (text-fig. 16, F, G). General Conclusions. The conclusions of general interest which have suggested them- selves in the course of the investigations above detailed are subjoined in the order of their importance :— 1. In the case of Tursius the structure of the upper lip and of the nose severs the genus completely from the Lemurs and brings it into line with the Pithecoid Primates. Taking this character in conjunction with the nature of the placenta, the presence of the postorbital partition, and other well-known features, it seems that Hubrecht was quite right in removing Yarsius from the Lemurs and placing it in the higher grade of Primates. I pro- pose to give practical expression to this view by dividing the Primates into two great series. For the first, comprising the Lemurs, the old name SrREPsIRHINT is available. For the second, comprising Zarsius and the Pithecoidea, I suggest the title Hartoruini. The Haplorhini will contain two divisions, the ‘Tarsioidea and the Pithecoidea *. 2. With Zarsius eliminated from the Lemurs, the Strepsirhini may be divided into the Chiromyoidea and the Lemuroidea. It has been the fashion of late years to depreciate the characters of Chiromys. Dy. Standing indeed gave the genus merely subfamily rank under the Indriside, the latter being equivalent to the Lemuride. But that classification sacrificed the characters of Ohiromys to the hypothesis that the genus is a specialised off- shoot of the Indrisoid stock. That may be true. Nevertheless, the specialisation has proceeded so far, and in so many directions, that it appears to me impossible to dispute the claim that the Lemuride and the Indriside are much more nearly akin to each other than either is to the Chiromyide. In the description of Chiromys the peculiarities of the teeth generally distract attention from the curious cranial modifications correlated with the rodent dentition, such as the immense size of the premaxille, which reach the lachrymals and exclude the reduced maxillee from con- tact with the nasals; also the absence of the bony ridge closing the glenoid behind and the longitudinal extension of the man- dibular condyle, two correlated characters subservient to the back and forth movement of the mandible well known in the * I prefer this name to Anthropoidea because in ordinary terminology the title “anthropoid,” reasonably according to its meaning, has become restricted to the man-like Apes. A marmozet can hardly be called “ anthropoid,” with any approach to the real meaning of the word. But a marmozet and a man are Ele Saniliecoels 52 MR. R. I. POCOCK ON ‘THE EXTERNAL Rodentia. These cranial features distinguish Chiromys from all Lemurs ; and when taken in conjunction with the teeth, with the: peculiarities of the hands and feet, and of the sublingua, they out- weigh, in my opinion, the known differences between the true Mascarene Lemurs (Lemuride and Indriside) and the Asiatic and African Galagos, Pottos, and Lorises. 3. With regard to the Galagos, Pottos, and Lorises, I am only acquainted with one invariable cranial character distinguishing them from the Lemuride and Indriside. This was pointed out by Forsyth Major and has been briefly expressed by Mr. Gregory * as follows :—In the Asiatic forms the ectotympanic is enlarged and external to the bulla of which it forms the outer wall. “In the Mascarene forms the ectotympanic is inclosed within the bulla, forming a ring or horseshoe. To this difference may be added tne one pointed out above in connection with the clitoris, which in the Asiatic genera is traversed by the urethra, whereas in the Mascarene forms the urethra opens above the tip of the clitoris. In view of these facts, I should divide the Lemuroidea into two series, for which Mr. Gregory’s names Lemuriformes for the Lemuridz and Indvisidee, and Lorisiformes for the Loriside (or Nycticebide) and the Galagidee may be adopted. Similarly for the subdivision of the Lemuride I follow Mr. Gregory in relegating the genera to two subfamilies, the Lemurine and Chirogaleine ; but I cannot agree with him that /Zapalemur belongs to the Chirogaleine. That genus appears to me to be essentially a Lemurine, its inclusion in the Chirogaleine spoiling the definition of the subfamily. 4. As a matter of minor interest it is quite clear that the genus Lemur as generally admitted and as recognised in this paper is susceptible of division into two or three genera. L. catta, for instance, differs from the other species in having the glands. on the fore-limb and the naked heel and seroma, aad also in the structure of the vulva. JZ. variegatus is also peculiar in the structure of the vulva. Furthermore, the Galagos of the G. senegalensis- type may be distinguished by the str ucture of the penis from that of the crassicaudatns- type. Generic names. appear to be available for these subdivisions of emer and Galago; but I do not propose to enter into that question now. My views above set forth differ in so many particulars from those of Mr. Gregory that it may be interesting to tabulate our classifications side by side, omitting those he adopts based upon extinct genera, which, so are as I am aware, do not materially affect the arrangement of recent forms. * Bull. Geol. Soc. Amer. 26, pp. 432-436, 1915. See also Bull. Amer. Mus. Nat. Hist. 35, pp. 266-267, 1916. CHARACTERS OF THE LEMURS AND TARSIUS. D3 Gregory, 1915-1916. Pocock, 1918. ‘Order PRIMATES. Subord. LEMUROIDEA. | Order PRIMATES. Grade STREPSIRHINI. Series LEMURIFORMEs. | Subord. LEMUROIDEA. Fam. Lemurip™. | Series LEMURIFORMES. Subfam. Lenwrine. Fam. LEMURIDS. , & Chirogaleine. | Subfam. Lemurine. Fam. INDRISID2. » Chirogaleine. » CHIROMYID®. Fam. INDRISID&. ‘Series LORISIFORMES. Series LoRISIFORMEs. Fam. Lorisip®. RaeloRranpe Subfam. Lovisine. Comics oy) f ab. Galagine. i I Subord. CHTROMYOIDEA. Sas yy =) | Series TARSITFORMES. | Fam. CHIROMYID ®. Fam. TARSIID2. ; Grade HAPLORHINI. ‘Subord. ANTHROPOIDEA. Subord. TARSIOIDEA » PITHECOIDEA. Apart from the removal of Zarsius from the Lemuroidea and the union of the Loriside and Galagide in a group equivalent to the Lemuride and Indriside combined, my classification agrees in the main with the classification published in Flower and Lydekker’s ‘Mammals,’ and in other works of about that period. ‘Of more recent classifications it appears to me that Gadow’s (Class. of the Vertebrata, 1898, pp. 52-53), although brief, ex- presses the facts with the nearest approach to the truth, especially in the primary division of the Primates into the three suborders Lemures, Tarsii, and Simiz. tie 2 ee ON THE PYRALID#, SUBFAMILY HYPSOTROPINA. 5 | 5. A Classification of the Pyratipa, subfamily Hypso- TROPINZ. By Sir Grorck Hampson, Bart., F.Z.8. [Received February 19, 1918: Read March 5, 1918.] Proboscis aborted or absent ; palpi upturned, oblique or down- curved, the males of the species with the maxillary palpi brush- like and contained in a hollow of the labial palpi usually having the palpi oblique in the male and downcurved in the female; maxillary palpi small and filiform, well developed and more or ‘less dilated with scales at extremity, or brush-like and contained in a hollow of the labial palpi; frons smooth, with tuft of hair, or prominences of various forms; antenne of male ciliated, laminate, serrate or pectinate with uniseriate branches, the basal joint often dilated and the shaft often downcurved at base with a ridge of scales in its sinus; the build slender; tibiz with all the spurs present; abdomen smoothly scaled. Fore wing narrow; vein la separate from 16; le absent; veins 2, 3 rarely stalked; vein 4 often absent or stalked with 5, 3 and 5 stalked or from the cell; 6 from below upper angle; 7 absent ; 8,9 and often 10 stalked or 9 absent, rarely 10 also absent, 8 given off before or after 10; 11 from cell. Hind wing with the median nervure pectinated on upper side; veins la, b,c present; 2 from near or well before angle of cell; veins 3 and 4 sometimes absent, or 3 and’5 stalked or from the cell, 4 often absent, or 3, 4, 5 all present, 4 stalked with 5 or from cell; 6, 7 stalked or from upper angle of cell; 8 anastomosing with 7 or approximated to it but free. The larve of very few species are known; these live on Graminacee and pupate in the ground in a chamber formed by agglutinated particles of the soil; Hmmalocera depressella, however, is injurious to sugar-cane, the larva feeding in its roots. The subfamily is a development from the Anerastiane—Ane- rastia Hiibn. Verz. p. 367 (1827), type dignella Hibn.—from which it differs only in the proboscis being absent or aborted and non-functional. The types of the new species are in the British Museum, the species of which the types are in the collection are marked with at, and those not in the collection with a *. No quotations from German authors published since Aug. Ist, 1914 are inserted. ‘* Hostes humani generis.” SIR GEORGE HAMPSON ON THE "p.La00) DULuUiaT | ‘pyoohjog ‘vy0ucboy “vrovsc “DULogVg =“ rN07AA suomuay aay “piyuodfoosy “DUIDT * ee —pispzy dog “DUT Se re ‘vdoujojdvg ‘pdououzy “vifrrg ‘sapnoyznupye wa ity “phoquy aaoUEaS “DiyyUoLfissog — saiaae ‘pdo.wjzownpn) “DIyUaInnT ‘paaspupg —“wshayoopoyy SS a -edatpona “aan “DIDU0PLOY | ‘pdo.zosdh fy among : | “DZOSVAV NT “pduny, — ‘pigaydiposa yy ama “pdotjoary ‘DUSDLIULT, | “DULDnaS | | 26 ‘paquagr ‘pipisozy “v.t ar “DIyINUa LT ‘VlajDQ ‘DoLyaoUa quad 2pisor @) ty I 1°09 Y 10) WNICOULOSAAF - HHL Ao ANHDOTAH PYRALIDA, SUBFAMILY HYPSOTROPIN A. Key to the Genera. ‘A. Hind wing with veins 3 and 4 absent. a. Fore wing with vein 8 from 9 before 10, 3 and 5 stalked ...... b. Fore wing with vein 8 from 9 after 10. ° al, Fore wing with veins 3 and 6 stalked. a2. Palpi upturned b2. Palpi oblique, straigh c2, Palpi downeurved BT Coenochroa, [p. 58. Menuthia, p. 60. . Calera, p. 59. b1, Fore wing with veins 3 and 5 from the cell. a2, Palpi upturned 62. Palpi porrect. - a3, Fore wing with vein 9 absent, 11 and 10... 63, Fore wing wi th yein 9 present, 11 from cell ........... Statina, p. 59. . Tinerastia, p. 61. stalked with 8 c. Fore wing with vein 10 from the cell ................:.0.0 ee 3B. Hind wing with vein 3 present, 4 absent. a. Fore wing with vein 4 absent. al, Fore wing with veins 9 and 10 absent, 8 from cell, 3 ‘and < 5 from cell ae 61, Fore wing with v from cell ........ cl, Fore wing with ve ein 9 absent, 10 from cell, 3 and 5 Calamnotropa, A _ Ceenotropa, p.89. Mesodiphlebia, [p. 61. [p. 91. Tampa, p. 62. . Bandera, p. 89. ad). Kore wing with vein 8 from 9 atter 10. a2, Fore wing with veins 3 and 5 stalked. a®, Palpi upturned. at, Frons with rounded prominence .............0....05+6 b4. Frons without prominence, a>, Palpi reaching to above vertex of head, the 2nd joint slenderly scaled ...............-00eeeses eee: b5, Palpi not reaching to above vertex of head, the Qund joint broadly scaled ..............1-0..00ee eee 63, Palpi oblique or downcurved. at, Frons with corneous plate produced to two slight TOMS 1m INOME 65 sc0c0a000re0 aunon0cd0o90a02N87.000900000 00 b4. Frons without corneous plate ....................000:- b2, Fore wing with veins 3 and 5 from cell. a3, Hind wing with veins 3 and 5 stalked 63, Hind wing with veins 3 and 5 from the cell. a+, Palpi upturned b+. Palpi downcurved .... ce}, Fore wing with vein 10 from the cell, 8 and 9 stalked. — a2. Hind wing with veins 3 and 5 stalked. a3. Frons with flattened corneous plate, rather trifid im front and produced to short lateral points, a cor- neous plate below the frons .......... Labo 63, Frons with pointed conical prominence ...... ©, Frons with long truncate corneous process with raised rim at extremity ........ a3, Frons with rounded prominence with raised rim at e’. Frons without prominence .)..............:0:e ee 62, Hind wing with veins 3 and 5 from the cell. a3, Hind wing with vein 8 anastomosing with 7 3, Hind wing with vein 8 not anastomosing with 7 2. Fore wing with vein 4 present. a}, Fore wing with vein 10 stalked with 8. a2. Fore wing with veins 4, 6 stalked or from a point. a3, Hind wing with vein 2 from or from close to angle of cell. a+, Frons with conical prominence GRRROWINAG Phyo uog oon dan eaadoodoowad oon edoboado Baolevooau oud ou 64, Frons without prominence. a. Frons with long pointed tuft of hair ............... 65, Frons without tuft of hair . Hypsotropa, [p _.. Sudania, p. 88. . Rhodochrysa, in 8from 9 before 10,3 and 5 stalked... Hosidia yp. 63. Dembea, p. 64. Ceara, p. 63. Leotropa, p. 64. . Alamosa, p. 65. Navasota, p. 6d. 67. R8. LP [p. 78. . Raphi metopus, Chortoneca, [p. 80. Metacrateria, [p. 79. Prinanerastia, [p. 80. _ Rhinaphe, p. 82. Laurentia, p. 90. Epidauria,p. 91. . Fossifrontia, [p- 107. Aurora, p. 106. . Commotria, [p. 107. 58 SIR GEORGE HAMPSON ON THE 63, Hind wing with vein 2 from well before angle of cell. a‘. Frons with rounded prominence ........................ Siboga, p. 112. 64. Frons without prominence. a. Fore wing with veins 4, 5, hind wing with veins 3and 5 stalked ......... ....... Ematheudes, es wing with veins 4, 5, hind | wing - with veins [p. 114. 3 and d from angle of cell .. Ric . Baptotropa, 62, Fore wing with veins 4, 5 separate. [p. 116. a’. Hind wing with vein 2 from near angle of cell......... Biafra, p. 114. 63, Hind wing with vein 2 from well before angle of cell. [p. 116. a+, Hind wing with vein 8 anastomosing with 7 ...... Ethiotropa, 64, Hind wing with vein 8 not anastomosing with 7 ... Patna, p.117. b!, Fore wing with vein 10 from the cell. a>. Fore wing with veins 4, 5 stalked. a’, Hind wing with veins 3 and 5 stalked .......... . Saluria, p. 93. 63. Hind wing with veins 3 and 5 from the cell ... » dep ophtasia, 6°. Fore wing with veins 4, 5 from the cell. [p. 104. a’, Hind wing with veins 3 and 5 stalked; frons with truncate “conical prominence Sag ot voce... Megalophota, 63, Hind wing with veins 3 and 5 from the cell. [p. 117. at. Frons with prominence hollowed out in front ...... Martia, p. 118. 64, Frons with disk of scales ....5) 00. ..c...csecse.ss 00-6. 4. -Discofrontia, [p. 118. c#, Frons without disk of seales or prominence ......... Critonia, p. 119. C. Hind wing with vein 4 present. a. Fore wing with vein 10 stalked with 8. [p. 121. a}, Hind wing with vein 8 anastomosing with 7 ............... Monoctenocera, 61, Hind wing with vein 8 not anastomosing with 7............ Saborma, p. 122 6. Fore wing with vein 10 from the cell. a\, Fore wing with veins 2, 3 stalked .............................. Osacia, p. 1238. 61, Fore wing with veins 2, 3 from the cell. a, Frons with small rounded prominence with a corneous OVENS ENON TI cock soncadanancneogouaveadoobedmnanebaueoonscadea JAUAOTOIOHOEy 63. Frons without prominence, (ip. 123. a‘. Fore wing with veins 4,.5 stalked ..................... Polyocha, p.124. 64. Fore wing with veins 4, 5 from the cell ............... Emmatocera, Tp. 126. Genus CaNocHRoa. Type. Conochroa Rag. N. Am. Phye. p. 20 (1887) ...... californiella. Petaluma Wulst, Trans. Am. Ent. Soc. xvii. Dev 2LOUGL SOO) erate fo aas mets vba astle sprees openly Sei libella. Proboscis absent; palpi downcurved, about three times length of head and thickly scaled; maxillary palpi minute and filiform ; frons with conical prominence, thickly scaled above ; antenne of male laminate and almost simple: Fore wing narrow and elongate, the apex rounded; vein 2 from close to ‘angle of cell; 3 and 5 strongly stalked, 4 absent; 6 from well below upper angle; 8, 9, 10 stalked, 8 from before 10; 11 from cell. Hind wing with vein 2 from close to angle of cell; 3 and 4 absent, 5 sometimes not reaching the termen; 6, 7 from upper angle ; 8 strongly anastomosing with 7. (1) *Ca:nocHROA ILLIBELLA. Anerastia illibella Hulst, Ent. Am. ili. p. 138 (Oct. 1887) ; Rag. Rom. Mém. viu. p. 419, pl. 45. £.9; Dyar, Cat. Lep. N. Am. p. 440. Cenochroa puricostella Rag. N. Am. Phye. p. 20 (Dec. 1887). U.S.A., Texas, Arizona. PYRALIDH, SUBFAMILY HYPSOTROPINA@, 59 (2) Ca&NocHROA INSPERGELLA. Cenochroa inspergella Rag. N. Am. Phye. p. 20 (1887);_id. Rom. Mém. viii. p. 419, pl. 45. f. 10; Dyar, Cat. Lep. N. Am. p. 440. U.S.A., Texas, Colorado, Arizona. | (3) *CaNOCHROA CALIFORNIELLA. Cenochroa californiella Rag. N. Am. Phye. p. 20 (1887); id. Rom. Mém. viii. p. 420, pl. 45. f.8; Dyar, Cat. Lep. N. Am. p. 441. U.S.A., Colorado, California, Arizona; Mexico, Presidio. Auctorum. Cenochroa monomacula Dyar, Pr. U.S. Nat. Mus. xlvii. p. 348: (GUOMES GAN e skal nu nvum te trea eu cRUhen crema iannn inate PANAMA. Genus CALERA. nN ype. Calera Rag. Nouv. Gen. p. 50 (1888) ............ punctilimbella. Proboscis aborted and minute; palpi downcurved, extending about twice the length of head and smoothly sealed ; maxillary palpi minute and filiform; frons smooth; antennz of male somewhat laminate and ciliated, the basal joint somewhat en- larged and flattened on outer side. Fore wing long and narrow,, the apex rounded; vein 2 from near -angle of cell; 3 and 5 strongly stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from elose to angle of cell; 3 and 4 absent; 6, 7 stalked ; 8 anastomosing strongly with 7. CALERA PUNCTILIMBELLA. Calera punctilimbella Rag. Nouv. Gen, p. 50 (1888); id. Rom. Mém. viii. p. 417, pl. 40. f. 20; Dyar, Cat. Lep. N. Am. p. 441. U.S.A., N. Carolina, Iowa, Texas. Genus STavrna. Type. Statina Rag. N. Am. Phye. p. 19 (1887) ......... roseotinctella. Proboscis aborted and minute; palpi downcurved, extending about two and a half times length of head and rather roughly sealed; maxillary palpi minute, filiform; frons with tuft of scales ; antenne of male Jaminate and ciliated, the shaft thickened with scales above at base, the basal joint long, dilated and flattened. Fore wing long and narrow, the apex rounded ; vein 2 from near angle of cell; 3 and 5 strongly stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10, 11 from cell. Hind wing with vein 2 from close to 60 SIR GEORGE HAMPSON ON THE angle of cell; 3 and 4 absent; 6, 7 from upper angle; 8 anasto- mosing strongly with 7. (1) *Srarina GAUDIELLA. Statina gaudiella Hulst, Trans. Am. Ent, Soc. xvii. p. 216 (1890); Rag. Rom. Mem. viii. p. 415, pl. 51. f.5; Dyar, Cat. Lep. N. Am. p. 440. U.S.A., Texas. (2) SravTINA ROSEOTINCTELLA. Statina roseotinctelia Rag. N. Am. Phye. p. 19 (1887); id. Rom. Mém. vii. p. 416, pl. 47. f. 7; Dyar, Cat. Lep. N. Am. p. 440. U.S.A., Florida, Texas. (3) TSTATINA PUNCTILINEELLA. Statina punctilineella Hmpsn. Rom. Mém. viii. p. 416, pl. 52. elisa @OON)): S. Brazin. (4) PSTATINA BIFASCIELLA. Statina bifasciella Hmpsn. Rom. Mém. viii. p. 416, pl. 52. f, 8 (1901). U.S.A., Texas. (5) STATINA RHODOBAPHELLA. Statina rhodobaphella Rag. Nouv. Gen. p. 50 (1888); id. Rom. Mem. viii. p. 417, pl. 45. f. 6. CELEBES, Sangir I.; N. GuinEA; QUEENSLAND. (6) TSTATINA ROSINELLA, sp. n. Q. Head and thorax purplish pink; abdomen whitish suf- fused with red-brown, dorsally fulvous towards base; antenne, pectus, and legs whitish tinged with red-brown. Fore wing purplish pink, the veins streaked with white; a brown shade below basal half of cell. Hing wing ochreous white. N. Nigeria, Minna (Macfie), 1 2 type. Hap. 16 sar (7) TSravTINa CASHMIRALIS. Statina cashmiralis Hmpsn. J. Bomb. Nat. Hist. Soe. xv. p. 20 (1901). KASHMIR, Genus MENUTHIA. Type. Menuthia Rag. Nouv. Gen. p. 50 (1888) ............... nanella. Proboscis absent ; palpi upturned to far above vertex of head, slender and smoothly scaled; maxillary palpi filiform; frons PYRALID&, SUBFAMILY HYPSOTROPINA. 61 smooth ; antenne of female almost simple. Fore wing long and narrow, the apex rounded; vein 2 from angle of cell : 3 and 5 stalked, 4 absent; 6 from Tnelaw upper angle ; ‘sh We 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with the cell short veins 2 and 5 stalked, 3 and 4 absent; 6, 7 from upper angle ;. 8 strongly anastomosing with 7. *VIENUTHIA NANELLA. Menuthia nanella Rag. Nouv. Gen. p. 50 (1888); id. Rom. Mem. viii. p. 418, pl. 40. f. 22 ZANZIBAR. Genus TINERASTIA. Type. Tinerastia Hmpsn. Rom. Mém. vii. p. 414 (1901)... Siecle. Proboscis absent; palpi upturned to rather above vertex of head and nearly smoothly scaled; maxillary palpi minute and filiform; frons with rounded prominence ; antennee of male laminate and ciliated, the basal joint rather long. Fore wing rather long and narrow, the apex rounded ; vein 2 from towards angle of cell; 3 and 5 from an gle, 4 absent ; 6 from below upper angle ; 8,9 , 10 stalked, 8 from beyond 10; s from cell. Hind wing with seins 2 and 5 from angle of cell, 3 and 4 absent; 6, 7 fo) stalked; 8 anastomosing strongly with 7. (1) TTINERASTIA DISCIPUNCTELLA, Menuthia discipunctella Hmpsn. Moths Ind. iv. p. 52 (1896) ; id. Rom. Mém. viii. p. 414, pl. 52. f. 10. CEYLON. (2) TTINERASTIA FISSIRELLA. Menuthia Jissivella Hmpsn. Moths Ind. iv. p. 52 (1896); id. Rom. Mém. viii. p. 414, pl. 52. f. 9. CEYLON. Genus MESODIPHLEBIA. : eee : ‘ Type. Mesodiphlebia Zell. Hor. Soc. Ent. Ross. xvi. PSPAIO Me iam seiocicier. Geet -lacisiocieluersie melmneracie nile san a ence crassivenia. Proboseis absent ; palpi porrect, about twice the length of head, almost straight and thickly scaled; maxillary palpi well developed and slightly dilated with scales ; frons with conical tuft of hair; antenne of male laminate and ciliated, the shaft somewhat curved at base and thickened with scales in the sinus, the basal joint rather elongate and flattened. Fore wing long and narrow, the apex apinilet 2 vein 2 from near angle of cell; 3 and 5 separate, 4 absent; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing rite veins 2 and 5 from angle of cell; 3 and 4 absent; 6, 7 from upper angle; 8 anastomosing strongly- with 7. 62 SIR GEORGE HAMPSON ON THE (1) *MEsopIPHLEBIA DELIQUELLA. Anerastia deliquella Zell. Isis, 1848, p. 861; Rag. Rom. Mém. viii. p. 413, pl. 45. f. 5. Anerastia trinotella Berg, An. Soc. Arg. 1885, p. 275. ARGENTINA. (2) TMESODIPHLEBIA CRASSIVENIA,. Anerastia crassiwenia Zell. Hor. Soc. Ent. Ross. xvi. p. 251, pl. xii. f. 52 (1881); Rag. Rom. Mem. viii. p. 415, pl. 40. f. 16. COLOMBIA: (3) MErsopIPHLEBIA STRICTICOSTELLA. Mesodiphlebia stricticostella Rag. Ann. Soc. Ent. Fr. 1887, yp. 260; id. Rom. Mém. viii. p. 413, pl. 40. f. 15. N. NicErIA; SUDAN. (4) + MESODIPHLEBIA ROSELLA. Calera rosella Hmpsn. Moths Ind. iv. p. 53 (1896) ; id. Rom. Mem. viii. p. 412, pl. 52. f. 7. Maopras, Nilgiris. (5) }MESODIPHLEBIA OCHRACEELLA, Sp. n. @. Head and thorax brownish ochreous; pectus, legs, and abdomen white suffused with brownish ochreous. Fore wing uniform brownish ochreous. Hind wing white with a faint ochreous tinge. ARGENTINA, Corrientes, Goya (Perrens), 1 2 type. Hap. 20 mm. Auctorum. Calera albicostella Grossbeck, Bull. Am. Mus. Nat. Hist. xxxvii. ps LOAs CIO TiN sv caecrecpees cee Maciocia L ts: U:S.A., Florida. Genus TAMPA. Type. Tampa Rag. N. Am. Phye. p.19 (1887) ....-.... dimediatella.. Proboscis aborted and small; palpi obliquely upturned to well above vertex of head and thickly scaled; maxillary palpi well developed and dilated with scales; frons smooth; antenne of male ciliated. Fore wing long and narrow; the costa highly arched, the apex rounded, the termen very oblique; vein 2 from close to angle of cell; 3 and 5 separate, 4 absent; 6 from below upper angle; 9 and 10 absent ; 11 from close to 8. Hind wing with vein 2 from near angle of cell; 3 and 5 strongly stalked, 4 absent; 6, 7 from upper angle; 8 anastomosing with 7 to mear apex. PYRALIDA, SUBFAMILY HYPSOTROPIN®. 63 TAMPA DIMEDIATELLA. Tampa dimediatella Rag. N. Am. Phye. p. 20 (1887); id. Rom. Mem. viii. p. 411, pl. 45. f.4; Dyar, Cat. Lep. N. Am. p. 440. U.S.A., Florida, Texas. Genus CEARA. Type. Ceara Rag. Nouv. Gen. p. 49 (1888) ».......5..... discinotella. Proboscia absent; palpi upturned to rather above vertex of head and moderately sealed ; maxillary palpi small and filiform ; frons smooth, with large conical tuft of scales ; antenne of male laminate and ciliated, the shaft with small tuft of scales above at base. Fore wing narrow, the apex rounded: vein 2 from angle of cell; 3 and 5 stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from near angle of cell; 3 and 5 strongly stalked, 4 absent; 6, 7 stalked; 8 strongly anastomosing with 7. (1) *CEARA DISCINOTELLA. Ceara discinotella Rag. Nouv. Gen. p. 45 (1888); id. Rom. Mém. viii. p. 368, pl. 39. f. 3. S. BRaAzIu. (2) TCEARA ALBIFASCIATA, Sp. n. 3. Head white; thorax white tinged with reddish brown ; abdomen white tinged with brown and dorsally with fulvous yellow towards base; pectus and legs white tinged with brown. Fore wing with white costal fascia narrowing to a point before apex and with vein 12 defined above and below by grey-brown, the area below it to just below the cell and vein 2 white suffused with grey-brown, leaving the veins streaked with white; the inner area pale pink with a white streak on vein |. Hind wing white, tinged with brown except on inner area. Br. BE. Arrica, Eb Urru (Betton), 1 3 type. xp. 26 mm. Genus Hosrpra. Type. Hosidia Hmpsn. Rom. Mém. viii. p. 408 (1901). ochrineurella. Proboscis absent ; palpi downcurved, extending about one and a half times length of head and roughly scaled ; maxillary palpi minute and filiform; frons smooth, with conical tuft of hair; antenne of male ciliated, the shaft with sinus and tuft of scales at base. Fore wing narrow, the apex rounded; vein 2 from clese to angle of cell; 3 and 4 stalked, 5 absent ; 6 from below upper angle; 8, 9, 10 stalked, 8 from before 10; 11 from cell. Hind wing with vein 2 from close to angle of cell; 3 and 5 strongly stalked, 4 absent; 6, 7 stalked: 8 anastomosing strongly with 7. ; 64 SIR GEORGE HAMPSON ON THE * HOsIDIA OCHRINEURELLA. Hosidia ochrineurella Hmpsn. Rom. Mém. vii. p. 409, pl. 45. fal a@i9 Os): Nata. Genus Dremsra. Type. Dembea Rag. Nouv. Gen. p. 45 (1888) ............ venulosella, Proboscis aborted and minute; palpi upturned to about vertex of head and thickly scaled; maxillary palpi minute and slightly dilated with scales; frons with large rounded prominence thickly clothed with scales; antennee of male laminate and ciliated, the: shaft with ridge of scales at base. Fore wing narrow, the apex rounded; vein 2 from towards angle of cell; 53 and 5 shortly stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from angle of cell; 3 and 5 stalked, 4 absent; 6, 7 stalked; 8 anas- tomosing strongly with 7. : +D»EMBEA VENULOSELLA, Dembea venulosella Rag. Nouv. Gen. p. 45 (1888); id. Rom. Mém. viii. p. 368, pl. 44. f. 19. N. Nigeria; AByssInIA; Br. C. AFRICA. Genus LEOrROPA, nov. Type, L. phenicias. Proboseis absent ; palpi obliquely upturned to about vertex of head and moderately scaled ; maxillary palpi minute and filiform ; frons smooth, rounded; antenne of male laminate and ciliated, with a sinus at base containing a double ridge of scales. Fore wing narrow, the apex rounded; vein 2 from towards angle of cell; 3and 5 stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from just before angle of cell; 3 and 5 very strongly stalked, 4 absent; 6, 7 stalked; 8 strongly anastomosing with 7. (1) tLEOTROPA PHGNICIAS, Sp. n. 3g. Head and thorax purplish pink; abdomen pale brownish grey dorsally tinged with fulvous; antenne brownish ; pectus, legs, and ventral surface of abdomen, except towards extremity, brownish tinged with purplish pink. Fore wing purplish pink, the veins streaked with white; a dark brown fascia through upper part of cell to apex, the costal area towards apex white. Hind wing brownish white ; a slight brown terminal line. Sierra Leone (Clements), 1 gd type. Hap. 22 mm. (2) tLEorroPA SARCINA, Sp. n. o. Head and thorax white mixed with ochreous brown ; abdomen white, dorsally faintly tinged with fulvous towards. PYRALIDAH, SUBFAMILY HYPSOTROPINA. 65 base ; pectus and legs white suffused with brown. Fore wing white tinged with purplish pink, the veins streaked with white ; the costa] area white narrowing to a point at apex and with vein 12 defined on each side by brown, a brown shade below the costal area. Hind wing white with a faint ochreous brown tinge on costal area and in submedian interspace. ‘ Br. EH. Arrica, Teita (Jackson), 1 5 type. Hap. 16mm. (3) tLEOTROPA PAPUANENSIS, Sp. n. 3. Head, thorax, and abdomen whitish suffused with reddish brown, the last dorsally tinged with fulvous towards base. Fore wing whitish irrorated with reddish brown, the costal area rather whiter, narrowing to a point at apex and with slight brown streak below it. Hind wing white slightly tinged with brown, the cilia white. | Dunc IN: Gunna, Ron I. (Doherty), 1 3 type. Hap. 14 mm. Genus ALAMOSA. Type. Alamosa Hmpsn. Rom. Mém, viii. p. 369 (1901). piperatella. Proboscis aborted and minute; palpi downcurved, extending about twice the length of head and thickly scaled; maxillary palpi minute and filiform; frons with flattened corneous plate produced to two slight points in front and thickly scaled above ; antenne of male laminate. Fore wing narrow, the apex rounded; vein 2 from towards angle of cell; 3 and 5 stalked, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from just before angle of cell; 3 and 5 strongly stalked, 4 absent ; 6, 7 from upper angle ; 8 strongly anastomosing with 7. » (1) ALAMOSA PIPERATELLA. Alamosa piperatella Hmpsn. Rom. Meém. viii. p. 369, pl. 51. f. 25 (1901). U.S.A., Colorado, New Mexico. (2) *ALAMOSA BIPUNCTELLA. Alamosa bipwnetella Barnes & McD. Contr. Nat. Hist. Lep. N. Am. ii. 4, p. 184, pl. 1. f. 7 (1913). U.S.A., Florida. ; Genus NAvASsora. / ‘Dype-. Navasota Rag. N. Am. Phye. p. 18 (1887) ............ hebetella. Proboscis aborted and minute; palpi extending about the length of head and moderately scaled, the 2nd joint oblique, the 3rd porrect ; maxillary palpi minute and filiform; frons smooth with conical tuft of hair; antenne of male laminate and ciliated, Proc. Zoo. Soc.—1918, No. V. Lia 66 SIR GEORGE HAMPSON ON THE the shaft with sinus at base containing a ridge of scales. Fore wing narrow, the apex rounded; vein 2 from towards angle of cell; 3 and 5 stalked, 4 absent ; 5 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind wing with vein 2 from close to angle of cell; 3 and 5 strongly stalked, 4 absent: 6, 7 stalked; 8 anastomosing with 7. (1) *NavAsora HEBETELLA. Navasota hebetella Rag. N. Am. Phye. p. 18 (1887); id. Rom. Mém. viii. p. 369, pl. 89. f. 5; Dyar, Cat. Lep. N. Am. p. 439. U.S.A., Texas. (2) rNAVASOTA PERSECTELLA, sp. N. @. Head and thorax purplish red; abdomen white, dorsally suffused with fulvous yellow towards base; pectus and legs white tinged with rufous. Fore wing purplish pink; the costal area creamy white, narrowing to a point at apex, vein 12 defined by the costa above it being purplish red and by a fine streak below, the costal area defined by a red-brown fascia below ; veins 4, 3, and | slightly streaked with white. Hind wing white slightly tinged with ochreous brown. Timor, Dili (Doherty), 1 2 type. Hap. 16 mm. (3) TNAVASOTA HAMAPHAELLA, sp. 1. Q. Head and thorax dusky crimson; abdomen fuscous, the base of dorsal area fulvous. Fore wing dusky crimson with a slightly defined rather paler costal fascia attenuated to a point before apex ; a very slight irroration of black scales and traces of a terminal series of points. Hind wing ochreous tinged with pale fuscous. LovisIAbDEs, St. Aignan I. (Meek), 1 9 type. Hap. 24 mm. (4) TNAVASOTA LEUCONEURELLA, sp. Nn. 3. Head and thorax dusky crimson; abdomen ochreous white. Fore wing crimson; the veins streaked with white, the subcostal and median nervures strongly so and the former defined on lower side by brown suffusion from base to apex. Hind wing yellowish white, the costal area tinged with fuscous. Ueanpa, Kampala (Ansorge) ; TRAnsvaaL, White R. (Cooke), 1g; Narat, Estcourt (Hutchinson), 1 $ type; Cart Conony, Transkei (diss /. Barrett),1 3. Hap. 24 mm. (5) tNAVASOTA CHIONOPHLEBIA, sp. Nn. Head and thorax purplish red mixed with some ochreous white; abdomen rufous, dorsally fulvous yellow on basal half ; pectus and legs whitish suffused with rufous. Fore wing purplish pink, the veins strongly streaked with white. Hind wing white tinged with rufous. PYRALID.E, SUBFAMILY HYPSOTROPINAE. 67 S. Nigerta, Yorubaland, Ogbomoso (Sir G@. Carter), 1 @ ; N. Nicerta, Zungeru (Simpson, Macfie), 2 2, Minna (Macfie), 13,19 type. Hap. 16-22 mm. (6) {NAVASOTA SYRIGGIA, sp. n. 2. Head and thorax rufous tinged with purplish pink, the metathorax ochreous white; abdomen fulvous yellow; pectus sand legs white, the latter tinged with purplish rufous. Fore wing pale purplish pink, the veins slightly streaked with white. Hind wing white with a faint ochreous tinge. ARGENTINA, Tucuman, Los Vasquez (Dinelly), 1 Q type. Hap. ‘24 mm. (7) NAVASOTA DISCIPUNCTELLA, Sp. 0. Q. Head, thorax, and abdomen white mixed with brown, the last faintly tinged with fulvous yellow towards base of dorsum. Fore wing white irrorated with fuscous brown and some pale purplish-pink scales ; a black discoidal point; a. slight blackish postmedial shade from vein 2 to inner margin. N. Nigeria, Minna (Maejie),1 2 type. Hap. 20 mm. Auctorun. Navasota myriolecta Dyar, Pr. U.S. Nat. Mus. xlvii. p. 347 (COSIS.net Ns oe AOE PANAMA. Genus Hypsorropa. = Type. Hypsotropa Zell. Vsis, 1848, p. 591 ............... lacie Heosphora Meyr. P. Linn. Soc. N.S.W. vii. Weel DON LOSZ items ten mecclaes see cetandasnesccaye psamathella. Seleucia Rag. Ann. Soc. Ent. Fr. 1887, p. 259. semirosella. JE OFOG IRE ING Nie leliny@s JOs IS) (CUSIST)) se scesaue approximella. Ambala Rag. Nouv. Gen. p. 45 (1888) ......... Suscostrigella. Lymira Rag. Nouv. Gen. p. 46 (1888) ......... semirosella. Tiarra Rag. Nouv. Gen. p. 46 (1888) ............ pusillella. Socora Rag. Nouv. Gen. p. 46 (1888) ............ tenwicostella. Talamba Rag. Nouv. Gen. p. 47 (1888) ......... tenuinervella. Wekiva Hulst, Trans. Am. Ent. Soc. xvii. Oe 2OACUSOO)) eps aae i AR areas eI luteicostella. Tinitinoa Dyar, Pr. U.S. Nat®.Mus. xlvii. et TR EL OMS \i ety. dU RG epee a one. Satoh lithe phyrdes. Proboscis aborted and minute; palpi typically obliquely up- turned to far above vertex of head, the 2nd joint fringed with scales in front; maxillary palpi slightly dilated with scales ; frons smooth, with tuft of scales; antenneze of male typically somewhat laminate and ciliated, the shaft slightly curved at base. Fore wing narrow, the apex rounded ; vein 2 from towards angle of cell; 3 and 5 separate, 4 absent; 6 from below upper angle; 8, 9, 10 stalked, 8 from beyond 10; 11 from cell. Hind 5* 68 SIR GEORGE HAMPSON ON THE wing with vein 2 from just before angle of cell; 3 and 5 strongly stalked, 4 absent; 6, 7 shortly stalked ; 8 strongly anastomosing with 7. Secr. J. Palpi of male upturned. 5 A. Palpi of male hollowed out to contain the brush-like maxillary palpi; the antennz with sinus and ridge of scales at base of shaft. a. (Ambala). Antenne of male with rather long uniseriate branches, the apex ciliated. (1) *HypsorroPpa CONTRASTELLA. Ambala contrastella Rag. Nouv. Gen. p. 45 (1888); id. Rom. Meém. viii. p. 370, pl. 38. f. 11. NATAL. (2) Hypsorropa FUSCOSTRIGELLA. Ambala fuscostrigella Rag. Nouv. Gen. p. 45 (1888); id. Rom.. Mem. viii. p. 371, pl. 38. f. 10. PuNJAB. (3) HypsorroPa SUBCOSTELLA, Sp. n. Head and thorax white, the tegule and patagia suffused with red-brown ; antenne red-brown; palpi irrorated with red-brown ; abdomen white, usually irrorated with brown and dorsally suf- fused with fulvous yellow towards base; legs irrorated with brown. Fore wing white with a faint pink tinge, and strongly irrorated with brown; an ochreous-brown fascia through the- cell from base to apex, extending to just below the cell. Hind wing white with a taint ochreous tinge. N. Nigeria, Zungeru (Mache, Simpson), 1 5, 2 9 type; Br. E. Arrica, N. Kavirondo, Maramas Distr., Ilala (Veave),. 26. Exp. 20-28 mm. (4) Hypsorropa PERVITTELLA, sp. 1. Head and thorax white mixed with red-brown; abdomen white tinged with red-brown and dorsally suffused with fulvous vellow towards base. Fore wing white thickly irorated with red-brown ; a red-brown fascia through the cell from base to apex, the veins below it streaked with white. Hind wing white with the costa tinged with brown towards apex. PungaB, Ajmere, 1 ¢ ; Bompay, Deesa (Vurse), 1 3, 1 9 type. Hap. 20 mm. 6. Antenne of male with uniseriate branches below the sinus only, then serrate. (5) HypsorropaA HETEROCERELLA. Hypsotropa heterocerella Himpsn. Moths Ind. iv. p. 54 (1896) ; id. Rom. Mem. viii. p. 371, pl. 52. f. 1. KASHMIR ; PUNJAB. PYRALIDH, SUBFAMILY HYPSOTROPIN ©. 69 ce. Antenne of male somewhat laminate and ciliated to base. (6) HypsorroPaA OCRACEELLA, Sp. Nn. go. Head and thorax brownish ochreous mixed with some white; abdomen ochreous white, dorsally tinged with fulvous yellow towards base. Fore wing brownish ochreous; a dark brown fascia along median nervure; a diffused antemedial line ‘from cell to inner margin ; a diffused dark postmedial line tend- ing to form streaks in the interspaces, oblique to vein 6, then inwardly oblique; a slight dark terminal lne. Hind wing white tinged with ochreous brown and with a dark terminal line to submedian fold. Trvor, Oinainisa (Doherty), 1 g type. Hap. 14 mm. B. Maxillary palpi of male filiform. a. Antenne of male with sinus at base of shaft containing a ridge of scales. a’. (Soeora). Palpi of male with the 2nd joint obliquely upturned and thickly , scaled, the third joint porrect. (7) *HypsorroPa TENUICOSTELLA. Socora tenuicostella Rag. Nouv. Gen. p. 46 (1888); id. Rom. Mulerins With, jo. BiG, yolle BS), igs Oe GAMBIA. b’. (Lymiva). Palpi of male slender, the 3rd jomt upturned. (8) *HypsorropaA SEMIROSELLA. Seleucia senirosella Rag. Ann. Soc. Ent. Fr. USSi7) pa2oep ide Rom. Mém. viii. p. 373, pl. 38. f.9; Staud. Cat. Lep. pal. 11. ‘p. 83. SYRIA. (9) Hypsorropa ILLECTALIS. Addyme illectalis Wik. xxx. 959 (1864); Rag. Rom. Mem. vin. pasts, pl. dot. o. Seleucia costatella Rag. Nouv. Gen. p. 46 (1888). BoRNEO; CELEBES. (10) tH yPsorRoPA BISCRENSIS, Sp. 0. , Head and thorax white tinged with red-brown; abdomen ‘creamy white, dorsally suffused with ochreous brown towards base. Fore wing white tinged with ochreous except a white costal fascia narrowing to a point at apex, defined below by a red-brown fascia; the median nervure and veins 5, 3 shghtly streaked with white. Hind wing creamy white. AucertA, Biskra (Walsingham), 1 3, 29 type, Hammam-es- Salahin (Walsingham), 13. Hap. 22-28 mm. (11) tHyPsorRoPA RHODOCHROELLA, Sp. n. Head and thorax deep rose-red; abdomen ochreous yellow, 70 SIR GEORGE HAMPSON ON THE dorsally fulvous yellow towards base; antenn fulvous yellow ; pectus, legs, and ventral surface of abdomen ochreous yellow suffused with brown. Fore wing deep rose-red, the costa and veins strongly streaked with white, the interspaces of costal area tinged with brown. Hind wing ochreous white slightly tinged with brown. 5 Hab. Ucanpa, Mulema (Doggett), 1 3, Ketoma (Doggett), 1 3; Br. C.Arrica, Mt. Mlanje (Weave),7 3, 3 2 type; TRAns- VAAL, White R. (Cooke), 1 3 ; Navan, Estcourt (Hutchinson), 23. Hap. 20-28 mm. (12) THypsorropa ALBIVENALIS. Ambala albivenalis Hmpsn. J. Bomb. Nat. Hist. Soc. xxi. p. 1250 (1912). CEYLON. d 6. Antennee of male without sinus at base of shaft containing a ridge of scales. a. (Hypsotropa). Palpi long; antennze of male with the shaft thickened at base. (13) *Hypsorropa LUTEICOSTELLA. Hypsotropa luteicostella Rag. N. Am. Phye. p. 19 (1887) ; Rom. Mém. viii. p. 376, pl. “30, (2 9; Dyar, Cat. Lep. N. ie p- 439. U,S.A., Florida. (14) rH ypsorropa OCHRICOSTELLA, Sp. h. 2. Head and tegule dark red-brown; thorax purplish red ;. abdomen fulvous yellow ; pectus, legs, and ventral surface of abdomen red-brown. Fore wing deep purple- -red ; a pale ochreous. yellow costal fascia narrowing to a point at apex, the costa tinged with purple-red and irrorated with a few dark scales to beyond middle, the costal fascia defined by diffused dark brown below. Hind wing reddish brown. MASHONALAND (Dobbie), 1 9 type. Hap. 20 mm. (15) fH ypsorroPa CHIONORHABDA, sp. N. Head and thorax black-brown mixed with some purplé-grey, especially on dorsum of thorax ; antenne whitish tinged with red- brown ; abdomen pale reddish brown with darker segmental lines ; pectus, legs, and ventral surface of abdomen grey suffused with blackish, the tibizw and tarsi in front white. Fore wing purplish grey irrovated with black-brown ; a silvery white costal: fascia narrowing to a point at apex and leaving the costal edge black towards ace defined below by a broad black-brown fascia with diffused lower edge. Hind wing grey suffused with reddish. brown and with darker terminal line. S. Nicerra, Yorubaland (Sir G. Carter), 13, 19; N. Nicerta, Zungeru (Macfie), 1 ¢; Ueanpa, Gondokoro (Reymes- Cole), 1 on Ketoma (Doggett), 2 3 ; Br. C. Arrica, Mt. Mlanje- PYRALIDH, SUBFAMILY HYPSOTROPINE. (a (Weave),5 $, 3 2, Luchenya R. (Weave), 6 5, 2 2 type, Ruo Valley (Weave), 1 ¢. Hup. 16-24 mm. (16) Hypsorropa INFUMATELLA. Hypsotropa infumatella Hmpsn. Rom. Mém. viii. p. 377, pl. 39. f. 8 (1901). TRANSVAAL; NATAL. (17) *Hypsorropa UNIPUNCTELLA. Hypsotropa unipunctella Rag. Nouv. Gen p. 47 (1888); id. Rom. Mém. viii. p. 377, pl. 38. f 12 ; Staud. Cat. Lep. pal. 11. p. 12. K. Srperia, Amurland. (18) tH yPsorroPa FUSIFASCIATA, sp. 1. ©. Head and thorax whitish suffused with red-brown ; abdo- men fulvous yellow, the ventral surface white tinged with red- brown. Fore wing whitish tinged with red-brown ‘and irrorated with blackish; a white costal fascia irrorated with blackish, rather diffused below, the costal edge blackish towards base ; a black discoidal point ; the terminal area suffused with blackish except at costa; cilia with a blackish line near base. Hind wing whitish strongly suffused with brown ; a fine dark terminal line and line near base of cilia. Cryton, Kandy (Green), 1 Q type. Hap. 18 mm. (19) *Hypsorropa ZOPHOPLEURA. Hypsotropha zophopleurw Turner, Pr. R. Soc. Queensl. xviil. p. 117 (1908). QUEENSLAND. (20) rH ypsorroPA PURPURELLA, sp. n. Head and thorax purple-pink; antenne fulvous yellow; palpi tinged with fuscous ; abdomen fulvous yellow; pectus, legs, and ventral surface of abdomen greyish suffused with fuscous, the claspers of male white. Fore wing purple-pink irrorated with black, the costa brownish ; a black spot in the cell near base; antemedial spots in the cell and on vein 1; obliquely placed spots at upper and lower angles of cell; a subterminal series of four spots, the spot at discal fold further from termen ; a terminal series of black points. Hind wing ochreous white; a terminal black line; cilia blackish at tips. Br. C. Arrica, Mt. Mlanje (Weave), 9 3, 3 2 type. Hup., 6 20, 9 22 mm. (21) Hypsorropa LIMBELLA. Hypsotropa limbella Zell. Isis, 1848, p. 591; Herr.-Schaff. Eur. Schmett. iv. p. 110, Tin. f, 38; Rag. Rom. Mém. vii. p- 376; Staud. Cat. Lep. pal. ii. p. 12. S. France; [rary ; Daumatra; Asta MINOR. 2 SIR GEORGE HAMPSON ON THE (22) Hypsorropa sYRIACELLA. Hypsotropa syriacella Rag. Nouv. Gen. -p. 46 (1888); id. Rom. Mém. viii. p. 377, pl. 39. f. 7; Staud. Cat. Lep. pal. ii. p. 12. Syria. (23) *Hypsorropa SOLIPUNCTELLA, Rees ee Rag. Rom. Mem. vii. p. 377, pl. 43. f, 23 (1901). joe (24) *Hypsorropa PAUCIPUNCTELLA. Hypsotropa paucipunctella Rag. Bull. Soc. Ent. Fr. 1895, p. cil; id. Rom. Mém. viii. p. 378, pl. 51. f. 10; Staud. Cat. Lep. joel, ile: jo 1}, Asta Minor, Taurus. (25) *Hypsorropa ICHORELLA. Anerastia ichorella Led. Verh. zool.-bot. Ges. Wien, 1855, p. 221) pls 3. £8); Rass Roms Mem. vii. pie3/8) ple 39) fale Staud. Cat. Lep. pal. p. 13. SYRIA. (26) Hypsorropa VULNERATELLA. Epischnia vulneratella Zell. Isis, 1847, p. 769: Rag. Rom. WUiSraals wikhle Os Bick jols BO, is JUL S Shaadi, Chins Ibe, joralls ile jos 1S. Anerastia ostrinella Lah. Bull. Soc. Vaud. vi. Contr. Faun. Sic. p. 396 (1861). » Hypsotropa roseostrigella Rag. Rom. Mém. viii. p. 379, pl. 39. it, LB CUO), SARDINIA; Srcity ; DauMatrra; SyRIA. (27) TH yPsoTROPA SCELETELLA. Anerastia sceletella Zell. Stett. Ent. Zeit. 1867, p. 404; Hmpsn. Moths Ind. iv. p. 54; Rag. Rom. Mém. viii. p. 379, pl. 44. f. 22. BrnGau, Calcutta. (28) Hypsorropa VERTHEIMSTEINI. Hypsotropa wertheimsteini Rebel, Rovart. Lep. xx. p. 171 (1913). HUNGARY. (29) TH yPsorROPA PUNCTINERVELLA, Sp. 0. Head and thorax pale ved mixed with whitish; abdomen creamy white, dorsally fulvous yellow towards base ; palpi rufous, white below towards base : pectus and legs er eamy white, the latter irrorated with some red-brown. Fore wing pale red slightly ‘ PYRALID®, SUBFAMILY HYPSOTROPIN®. (3 ‘irrorated with dark brown, the veins and costal edge white; a minute antemedial black spot on vein | and postimedial spots on veins 3, 2, 1; a terminal series of shght blackish points. Hind wing ochreous white. Cryton, Haputale (Alston), 1 5 type, Kegalle (Alston), 1 9, Hambantota (Pole),1 9. Hap. 14-16 mm. (30) HypsorropA ADUMBRATELLA. Hypsotropa adumbratella Rag. Nouv. Gen. p. 47 (1888); id. Rom. Mém. viii. p. 380, pl. 38. f. 13. GampBia; Naran; Carr CoLony. b!. (Tiarra). Palpishort; antennz of male with the shaft curved at base. (31) *HyPsorroPa. PUSILLELLA. Tiarra pusilleila Rag. Nouv. Gen. p. 46 (1888) ; id. Rom. Mém. Vili. p. 372, pl. 39. f. 4. ZANZIBAR. ‘Secr. IJ. Palpi of male porrect. A. (Lalamba). Palpi of male hollowed out to receive the brush-like maxillary palpi; antenne with sinus at base of shaft containing a ridge of scales. (32) HyPpsorroPpaA TENUINERVELLA. Talamba tenuinervella Rag. Nouv. Gen. p. 47 (1888); id. Rom. Mem. viii. p. 387, pl. 40. f. 25; Hmpsn. Moths Ind.iv. p.95. * PungaB, Kangra; Mapras, Nilgiris. B. Maxillary palpi filiform. a. Anteanze of male with sinus at base of shaft containing a ridge of scales. al. (Tinitinoa). Antenne of male pectinate with long uniseriate branches to middle. (33) *HypsorroPpA PHYRDES. Tinitinoa phyrdes Dyar, Pr. U.S. Nat. Mus. xlvi. p. 348 (1913). PANAMA. b’. (Heosphora). Antenne of male laminate. (34) *HypsorrRoPA PAPUASELLA. Heosphora papuasella Rag. Nouv. Gen. p. 47 (1888); id. Rom. Mém. xxiii. p. 382, pl. 39. f. 14. N. GuINnEA, (35) *HypsorroPA SABULETELLA. Anerastia sabuletella Zell. Lep. Micr. Caffr. p. 73 (1852); Rag. Rom. Mém. vill. p. 383, pl. 39. f. 18. Care Cotony. , 74 SIR GEORGE HAMPSON ON THE (86) tHyPsorroPa CREMORICOSTA, Sp. n. d. Head and thorax ochreous, the head and tegule suffused with purplish red ; antenne ochreous yellow ; abdoinen ochreous, dorsally fulvous yellow towards base ; pectus, legs, and ventral surface of abdomen purplish red. Fore wing pale flesh-red, deepening in colour towards the costal fascia which is ochreous white, narrowing to a point at apex, slightly defined by brown below and leaving the costal edge brown towards base. Hind wing ochreous white, the costal area and termen except towards. tornus deeper ochreous. U.S.A., Colorado, Colorado Springs (Cockerell), 1 eS Heep. 24 mm. (37) THyYPsOTROPA NIVEICOSTA, Sp. 0. @. Head and thorax white suffused with rufous except on dorsum of thorax; abdomen ochreous white, dorsally fulvous. yellow towards base ; pectus, legs, and ventral surface of abdomen white suffused with rufous. Fore wing pale flesh-red irrorated with a few red-brown scales and deepening to rufous towards the costal fascia, which is snow-white narrowing to a point at. apex and leaving the costal edge rufous towards base. Hind wing white with a faint ochreous tinge. ARGENTINA, Gran Chaco, Florenzia (Wagner), 1 2 type. Hup. 20 mm. (38) tH yPsorropa PERIPH#A, sp. 0. @. Head and tegule white tinged with red-brown; thorax pale purplish pink ; “abdomen white dorsally tinged w ith fulvous yellow towards base ; pectus, legs, and ventral surface of abdomen white tinged with red-brown. Fore wing pale purplish pink; a pure white costal fascia irrorated with afew brown scales towards. costa, narrowing to a point at apex and defined below by dark red-brown, diffused below. Hind w ing white with a faint ochreous tinge. N. Nieerra, Minna (Macfie), 2 2 type, Borgu, Yelwa Lake (Migeod),1 29. Hap. 16 mm. (39) tHypsorropa TRIPARTALIS, sp. nN. @. Head white suffused with rufous; thorax pale purplish pink; abdomen ochreous yellow; pectus and legs ochreous. yellow, the fore legs tinged with brown. Fore wing with narrow pure white costal fascia leaving the costal edge brown towards base, the area to discal fold red-brown and the area below it bright purplish pink. Hind wing white with a faint ochreous tinge. Formosa, Takow (Wileman), 1 2 type. Hap. 18 mm. (40) tHypsorTROPA LATERCULELLA. Anerastia laterculella Zell. Stett. Ent. Zeit. 1867, p. 403; PYRALID#, SUBFAMILY HYPSOTROPINAE. 75: Hmpsn. Moths Ind. iv. p. 55; Rag. Rom. Mém. viii. p. 383, pl. 44. f..21. BENGAL. (41) THypsorroPa ROSESCENS, sp. nh. ¢. Head and thorax purplish red-brown, the latter with the- dorsum grey-brown ; abdomen fulvous yellow ; pectus, legs, and ventral surface of abdomen whitish tinged with brown. Fore- wing pale grey-brown suffused with crimson-red, rather browner towards the costal fascia, which is white slightly irrorated with pale red and narrowing to apex. Hind wing white tinged with. ochreous brown. Cryion, Nawalapitiya (Green), 1 ¢ type. Hap. 20 mm. (42) *Hypsorropa STEREOSTICHA. Hypsotropha stereosticha Turner, Pr. R. Soc. Queens]. xix. p: 41 (1905). QUEENSLAND, Thursday I. (43) Hypsorropa ICASMOPIS. Hypsotropha icasmopis Turner, Pr. R. Soc. Queensl. xviii. p. 116: (1903). QUEENSLAND. (44) Hypsorropa EURYZONA. Hypsotropa euryzond Meyr. Ent. Mo. Mag. xix. p. 256 (1882) ; Rag. Rom. Mém. viii. p. 382, pl. 39. f. 13. S. AUSTRALIA. (45) Hypsorropa NIPHOPLEURA. Hypsotropha niphopleura Turner, Pr. R. Soc. Queens]. xxiv. Pelli Gots): N. AvstfRatia. (46) fH ypsorRoPA DIAPH#A, sp. n. @. Head and thorax black-brown, the frons and metathorax rufous; antenne rufous; palpi black with a greyish gloss; abdomen grey suffused with brown; pectus, legs, and ventral surface of abdomen grey suffused with blackish. Fore wing whitish ; the costal edge black with a flesh-red fascia below it to beyond middle, the area below the cell black with a whitish “streak along vein 1. Hind wing whitish strongly suffused with fuscous brown, the cilia whiter with a dark line near base. Br. C. Arrica, Mt. Mlanje (Weave), 1 9 type. Hap. 24 mm. (47) Hypsorropa DYSEIMATA. Hypsotropha dyseemata Turner, Pr. R. Soc. Queensl. xxiv. p- 112 (1918). Timor Laur; N. AUSTRALIA. 76 SIR GEORGE HAMPSON ON THE (48) Hypsorropa QUADRIPUNCTELLA. Hypsotropa quadripunctella Hmpsn. J. Bomb. Nat. Hist. Soe. xl. p. 307 (1897); id. Rom. Mém. viii. p. 384, pl. 39. f. 16. Pungas, Oude; Borneo; Puto Laur. (49) Hypsorropa PSAMATHELLA. p. 234 (1879); Rag. Rom. Mém. viii. p. 384, pl. 39. f. 15. TAnerastia nitens Butl. Trans. Ent..Soc. 1886, p. 440. QUEENSLAND; N.S. WALES. Anerastia psamathella Meyyv. Proc. Linn. Soc. N.S.W. iv. (50) TH YPSOTROPA MONOSTIDZA, sp. 1. 2. Head and thorax ochreous with a faint purplish pink tinge ; abdomen ochreous with a fulvous yellow tinge; pectus, legs, and ventral surface of abdomen ochreous with a brownish tinge. Fore wing ochreous faintly tinged with purplish pink -and irrorated with dark brown; a minute blackish discoidal spot. Hind wing white tinged with ochreous especially towards termen. SrERRA LEONE (Clements), 1 @ type. Map. 18 mm. (51) tH yPsorRoPA GRAPLOPHLEBIA, sp. n. 3. Head and thorax white mixed with purplish red-brown ; ‘abdomen white slightly tinged with brown; pectus, legs, and ventral surface of abdomen white suffused with red-brown. Fore wing white suffused with purplish red-brown and slightly irrorated with dark brown. the veins white defined on each side by fine dark brown streaks. Hind wing white tinged with -ochreous brown. MASHONALAND, Salisbury (Jarshall), 1 3 type. Hap. 20 mm. (52) TH yPSOTROPA POLYACTINIA. Heosphora polyactinia Hmpsn. Rom. Mém. viii. p. 384, pl. 52. fa2 LOO): UcanpDA; MASHONALAND; TRANSVAAL; Narat. (53) THyPsorropa ENDORHODA, sp. n. 2. Head and thorax ochreous suffused with purplish pink ; abdomen ochreous white, dorsally fulvous yellow towards base ; pectus, legs, and ventral surface of abdomen ochreous white suffused with red-brown. Fore wing with the costal half to median nervure and vein 5 ochreous, tinged with purplish pink towards costa and with slight pale streaks on the veins; the inner half purplish pink with slight white streaks on the veins. Hind wing white tinged with ochreous. N. Ruovesia (Coryndon), 1 2 type. Hxp. 24 mm. (54) HypsorropA RAMULOSELLA. Heosphora ramulosella Rag. Bull. Soc. Ent. Fr. 1895, p. eii; id. PYRALIDH, SUBFAMILY HYPSOTROPIN A. (LO. Rom. Mém. viii. p. 385, pl. 52. f. 3; Staud. Cat. Lep. pal. ii. Polit SYRIA, (55) HypsorropA LEUCOPHLEBIELLA. Heosphora leucophlebiella Rag. Nouv. Gen. p. 47 (1888); id. Rom. Mém. vii. p. 385, pl. 39. f. 17. Br. C. ArricA; MasHonatanp; TRANSVAAL; Nata; CAPE CoLony. (56) Hypsorropa RHODOSTICHA. Hypsotropha rhodosticha Turner, Pr. R. Soc. Queensl. xviii. p. 116 (1903). QUEENSLAND. b. (Peoria). Antenne of male without sinus and ridge of scales at base of shaft -(57) tHypsorROPA POLYSTICTELLA, sp. n. ¢. Head, thorax, and abdomen whitish suffused with rufous. . Fore wing ochreous white suffused with rufous in the inter- spaces leaving the veins pale; the costal edge black towards base ; a slight shade formed by black irroration below the costa to apex ; a small antemedial black spot on vein 1, a small spot on lower discocellulars and an oblique postmedial series of four small spots on veins 5, 3, 2, 1; a terminal series of small black spots. Hind wing white tinged with ochreous; a fine fuscous terminal line and slight brown line near base of cilia. Br. C. Arrica, Mt. Mlanje (Weave), 2 ¢ type. Haup. 20 mm. (58) *Hypsorropa ACNIDIAS. Hypsotropha acnridias Turner, Pr. R. Soc. Queensl. xvii. p. 117 (1903). QUEENSLAND. (59) THypsorropa APPROXIMELLA. Hurhodope approximella Wik. xxxv. 1722 (1866); Rag. Rom. Mém. viii. p. 386. pl. 40. f. 24; Dyar, Cat. Lep. N. Am. p. 439. Anerastia hematica Zell. Verh. zool.-bot. Ges. Wien, 1872, p- 955. Anerastia roscatella. Pack. Ann. N. Y. liyc. Nat. Hist. x. p- 270 (1870). U.S.A., Massachusetts, N. York, Pennsylvania, Ohio, Illinois, N. Carolina, Texas, Colorado. (60) THyPsorRoPA LEUCOCRASPIS, sp. Nn. 6. Head, thorax, and abdomen white suffused with ochreous . brown. Fore wing pale ochreous brown, the costal edge white. ind wine white tinged with ochreous brown especially on apica Hind eg white tinged with ocl I Ly pical area. ENTIN orrientes, Goya (Perrens e. Exp. 20 mm. . ARGENTINA, Corrientes, G IE, ,1 og type. Exp. 20 ‘78 SIR GEORGE HAMPSON ON THE (61) *HYPSOPROPA BIPARTELLA. Peoria bipartella Rag. N. Am. Phye. p. 19 (1887); id. Rom. Mém. viii. p. 386, pl. 40. f. 33; Dyar, Cat. Lep. N. Am. p. 439. U.S.A., N. Carolina. Auctorum. Peoria albidella Hulst, Can. Ent. xxxiii. p. 178 (1900); Dyar, Oem, Ibias IN, AWS JOs AY scudasdandosdegcss U.S8.A., California. Hypsotropha laropis Turner, Pr. R. Soc. Queens]. xxiv. p. 173 (GU IOs) ame mem SAS on nae bel cae ty sc Queensland. - neurica Turner, Pr. R. Soc. Queensl. xxiv. p. 113 (GOWNS Oe As Sree Rirc scien arsenate N. Australia. Gye Saluria armeniella Rag. Nouv. Gen. p. 44 (1888). AuGceRIA; ‘Tunis; ARMENIA; Cyprus; W.TuRKEStAN ; CEYLON. (59) FSALURIA PULVEROSA. Powjadia pulverosa Ampsn. Moths Ind. iv. p. 60 (1896); id. Rom. Mém. viii. p. 361, pl. 37. f. 3. SIND. PYRALID®, SUBFAMILY HYPSOTROPINA. 103 (60) *SALURIA MAGNESIELLA. Saluria magnesiella Rag. Nouv. Gen. p. 44 (1888); id. Rom. Mem. vii. p. 360, pl. 37. f. 18: Staud. Cat. Lep, pal. 1 p. 13 W. TuRKESTAN. b’. Antenne of male serrate and ciliated. (61) TSALURIA MESOMELANELLA, Sp. n. @. Head purple-red and black-brown ; thorax purple-red and whitish; abdomen whitish suffused with brown, dorsally rufous towards base; pectus, legs, and ventral surface of abdomen whitish suffused with red-brown and dark brown. Fore wing whitish tinged with purplish pink, the costa and termen deep purple-crimson, the medial area suffused with black except at costa, and the costa defined below by black; an antemedial black point on vein 1 with a purple-pink shade below it on inner margin; the inner edge of the medial black area obliquely curved and its outer edge bent inwards below submedian fold; cilia pale fuscous. Hind wing white tinged with brown especially at termen, the cilia with a fine brown line near base. TransvaaL, White R. (Cooke), 19 type. Hap. 28 mm. (62) SALURIA TRIPARTELLA. Saluria tripartella Rag. Rom. Mem. viii. p. 359, pl. 39. f. 19 (1901). TRANSVAAL; Navrat; BASUTOLAND. (63) SALURIA CALLIRHODA. Powjadia callirhoda Turner, Pr. R. Soc. Queensl. xvii. p. 120 (1903). QUEENSLAND. (64) TSALURIA INTERPUNCTELLA, Sp. 0. Head, thorax, and abdomen ochreous suffused with rufous; pectus, legs, and ventral surface of abdomen reddish ochreous mixed with brown, Fore wing ochreous suffused with rufous ; the veins white defined on each side by fine black-brown streaks, the submedian fold and vein | defined by fine rufous streaks ; the costal edge black towards base; an antemedial blaek point on vein |, a point in lower angle of cell, an oblique postmedial series in the interspaces, incurved beiow submedian fold and a terminal series. Hind wing ochreous with a fine brownish terminal line except towards tornus. MASHONALAND (Dobbie), 2 5,2 2 type; TransvaaL, Kvanspruit (Janse), 1 2, Pretoria (Distant), 192. Hap, 20-24 mm. (65) TSALURIA INSIGNIFICELLA, sp. n. @. Head and thorax white mixed with red-brown ; abdomen white tinged with brown, dorsally fulvous yellow towards base. 104 SIR GEORGE HAMPSON ON ‘THE Fore wing whitish tinged with red-brown, especially towards costa; the costa narrowly white. Hind wing white tinged with red-brown. PARAGUAY, Sapucay (/oster), 19 type Hap. 18 mm. Auctorune. ¢ Atascosa quadricolorella Dyar, Proc. Ent. Soc. Wash. vi. p. 114 (1904). Sect. Poujadea” 5.4. ies U.S.A., N. Mexico. Powjadia pimella Dyar, J. N. Y. Ent. Soe. xiv. p. 31 (1906). U.S.A., Arizona. Pectinigeria pamponerella Dyar, Proc. Ent. Soc. Wash. x. p. 107 DOB) a caret cccse ase ncstate dace wey ie eo ce yee U.S.A., Colorado. Ollia parvella Dyav, J. N. Y. Ent. Soe. xiv. p. 31 (1906). Sect. SMUG CGMS ANA IAB 08 The BYE Sik ea E SE eA ER U.S.A., Texas: Ollia honoponerella Dyarv, Proc. Ent. Soc. Wash. x. p. 107 (IDOE) o> SSRI SGU 28 obo sdeSsies Scoccosobe kn U.S.A., Arizona. Ollia santaritella Dyar, J. N. Y. Ent. Soc. xii. pp. 107-8 (1904). BCLS (CLUuI UG tee man omen tee bi ar actaisane ces Aanon U.S.A., Arizona. Poujadia leuconeura Turner, Pr. R. Soc. Queensl. xxiv. p. 118 (EQS) Ja GSC, Ia OHNTHECD sobsoceoc sdaoeo desea N. AUSTRALIA. Pectinigeria violodis Dyar, Pr. U. 8. Nat. Mus. xlvil. p. 347 CUGUS) is cauttian Seaumciacantatte aun i anst cy nen ep Reem PANAMA. Powadia cyttarella Dyar, Pr. U.S. Nat. Mus. xlvii. p. 347 (GQIIES NUR cer aesciace cree eters ae tan aise a Ee PANAMA. Genus PRopHTAsSrA. Type. Prophtasia Rag. Ann. Soc. Hunt. Fr. 1887, p. 259... platycerella. Proboseis aborted and minute; palpi typically obliquely up- turned, the 3rd joint porrect; maxillary palpi filiform ; frons smooth, with slight tuft of scales; antenne of male typically laminate, the shaft slightly curved at base and without distinct ridge of scales. Fore wing long and narrow, the apex rounded, the termen evenly curved ; veins 2 and 3 typically from angle of cell; 4, 5 stalked; 6 from below upper angle; 8, 9 stalked ; 10, 11 from cell. Hind wing with vein 2 from well before angle of cell; 3 and 5 from angle, typically approximated for some distance, 4 absent ; 6, 7 shortly stalked; 8 typically not anasto- mosing with 7. Sect. I. Fore wing with veins 2, 3 from a point at angle of cell; hind wing with vein 8 not anastomosing with 7. (1) PRoPHTASIA PLATYCERELLA. _ Prophtasia platycerella Rag. Ann. Soc. Ent. Fr. 1887, p. 259 ; id. Rom. Mém. viii. p. 252, pl. 37. f. 8; Staud. Cat. Lep. pal. ide peml Be ARMENIA, PYRALID#H, SUBFAMILY HYPSOTROPINA. 105 Secor. II. Fore wing with vein 2 from well before angle of cell, 3 from before angle ; hind wing with veins 3 and 5 not approximated towards base. A. Hind wing with vein 8 anastomosing with 7; palpi obliquely upturned and hardly reaching to vertex of head, the maxillary palpi filiform ; antennee of male with the shaft slightly curved at base and without distinct ridge of scales. (2) }PROPHTASIA SPHALMATELLA, Sp. Nn. ¢. Heal and thorax black-brown tinged with grey; abdomen brownish ochreous, dorsally fulvous yellow towards base, ventrally grey-brown. Fore wing black-brown mixed with some grey, especially on inner area; a pure white fascia on costal area, leaving the costa black-brown and not reaching the apex; an indistinct diffused dark antemedial spot on vein | and oblique postmedial line. Hind wing whitish suffused with brewn; a darker terminal line and white line at base of cilia. MASHONALAND, Salisbury (J/arshall), 1d type. xp, 28 mm. (3) PPROPHTASIA EPITEUXIS, sp. n. dg. Head and thorax glossy black-brown ; abdomen grey suf- fused with brown; palpi white below towards base ; pectus, legs, and ventral surface of abdomen black-brown, the femora and tibie streaked with white. Fore wing glossy black-brown, the inner area tinged with grey; a pure white costal fascia, narrow- ing toapex; an indistinct diffused dark antemedial line ‘ ‘om cell to inner margin and oblique postmedial line. Hind wing grey suffused with fuscous; a slight punctiform dark terminal line and white line at base-of cilia. Burma, Hsipaw (de Vicéville), 2 ¢ type. Hap. 24-28 mm. (4) 7PROPHTASIA GLAUCOPHA, Sp. n. Head and thorax grey-brown tinged with white; abdomen white suffused with grey-brown; palpi white in front except towards tips; peetus, legs, and ventral surface of abdomen white mixed with some brown. Fore wing pale grey-brown, black- brown towards the rather broad white costal fascia einen does not narrow to apex. Hind wing creamy white slightly tinged with brown. Kasumtr (Pilcher), 1 3; Punsas, Kangra (Dudgeon), 1 3, Moghal Sarai (Setion), 1 3 ; Beneau, Oudh (Pilcher), 1¢; Sip, Karachi (Swinhoe), 19 ; MaApras, Belgaum (Watson), 13 type. Hep. 18-22 mm. (5) TPROPHTASIA AMPHICHEA, Sp. n. Head and thorax grey-brown mixed with white; abdomen white tinged with brown; pectus and legs white mixed with brown. Fore wing pale purplish brown nied with white, the costal area broadly white with slight brown irroration ; indistinct diffused dark curved ante- and postmedial lines except towards 106 SIR GEORGE HAMPSON ON THE costa; two slight blackish discoidal spots. Hind wing white tinged with brown ; a slight dark spot at upper angle of cell and fine terminal line ; cilia w hiter. SIERRA LEONE (Clements), 1Sy4.O% N. Nigeria, Minna (Macfie), 1¢ type, Zungeru (Simpson), 12. Hap. 16-20 mm. B, Hind wing with vein 8 not anastomosing with 7. a. Palpi of male obliquely upturned to above vertex of head and hollowed out to receive the brush-like maxillary palpi, the 3rd joint porrect ; antennee serrate with sinus at base of shaft containing a large ridge of scales. 6) +r PROPHTASIA PYROSTROTA, Sp. n > 5] 3. Head and thorax creamy white suffused with rufous ; abdomen, pectus, and legs creamy white. Fore wing ochreous white irrorated with fiery red, the costal fascia only defined by a red-brown fascia below it from base to apex ; minute antemedial black streaks on median nervure and vein | and an oblique post- medial series ; two slight black discoidal spots ; a terminal series of black points. Hind wing creamy white. Pungas, Kangra Valley, 4500’ (Dudgeon), 1 3 type. Hap. 26 mm. 6. Palpi of female downcurved and extending about three times length of head. (7) PROPHTASIA BISTRIATELLA. Cayuga bistriatella Hulst, Trans. Am. Ent. Soc. xvii. p. 209 (1890); Dyar, Cat. Lep. N. Am. p. 438. Peoria discostrigella Dyar, Proc. Ent. Soc. Wash. vi. p. 115 (1904). U.S.A., N. Mexico, Arizona. Genus AURORA. Type. Aurora Rag. N. Am. Phye. p. 18 (1887)......... longipalpalla. Proboscis aborted and minute; palpi porrect, extending about four times length of head, thickly fringed with hair, fie 2nd joint slightly downcurved ; maxillary palpi shght and filiform ; frons smooth, with long pointed tuft of hair; autenne of female minutely ciated. Fore wing long and narrow, the apex rounded, the termen obliquely curved; vein 3 from elose to angle of cell; 4,5 strongly stalked; 6 from below upper angle; 8,9, 10 stalked ; 11 from cell. Hind wing with vein 2 from close to angle of cell ; 3 and 5 stalked, 4 absent; 6, 7 shortly stalked ; 8 anastomosing with 7. TAURORA LONGIPALPELLA, Aurora longipalpella Rag. N. Am. Phye. p. 18 (1887); id. Rom. Mem. viii. p. 337, pl. 44. f. 2; Dyar, Cat. Lep. N. Am. p. 437. U.S.A. PYRALIDH, SUBFAMILY HYPSOTROPINA. 107 Genus FosstrRoNTIA. : bi uaa ye Fossifrontia Hmpsn. Rom. Mem. viii. p. 388 (GTS AUILL)) see a Sa Pe ERE en ee leuconeurella. Proboscis absent; palpi upturned to about middle of frons, thickly scaled and hollowed out to receive the brush-like maxillary palpi; frons with truneate conical prominence hollowed out in front ; antenne of male uniserrate and ciliated, the shaft with large sinus and ridge of scales at base; fore femora with tuft of hair above, the mid tibize fringed with long hair on outer side. Fore wing narrow, the apex rounded, the termen evenly curved ; vein 3 from before angle of cell; 4,5 stalked; 6 from below upper angle; 8, 9,10 stalked; 11 from cell; the male with small fold on underside from medial part of costa fringed with large scales and with some androconia below it above, in and below the cell. Hind wing with vein 2 from towards angle of cell ; 3 and 5 from angle and closely approximated for some distance, 4 absent; 6, 7 shortly stalked ; 8 closely approximated to ¥ but not anastomosing with it. FossIFRONTIA LEUCONEURELLA, Fossifrontia leuconeurella Hmpsn. Rom. Mém. viii. p. 339, jolly BH, vig IS CLO) QUEENSLAND, Cooktown, Cedar Bay. Genus CoMMOTRIA. Type. Commotria Berg, An. Soc. Arg. xix. p. 278 i (USS) bce tence eee Meneame tnvenustella. Mangala Rag. Nouv: Gen. p. 41 (1888)......... crassiscapella. Tolima Rag. Nouv. Gen. p. 41 (1888) ......... oberthuri. Altoona Hulst, Ent. Am. iv. p. 116 (1888) ... omacella. Volusia Hulst, Trans. Am. Ent. Soc. xvii. - p. 206 (1890), nec Rob. Desv. Dipt. 1830... roseopennella. Trwolusia Dyar, Cat. Lep. N. Am. p. 438 (IDO DN art eee sae anny ne nc ants roseopennella. Proboscis absent ; palpi downeurved, extending about three times length of head and thickly scaled; maxillary palpi slight and filiform ; frons rounded and with short tuft of hair; antenne of male typically unipectinate, the apical part ciliated, the shaft with ridge of scales above at base. Fore wing long and narrow, the apex rounded, the termen obliquely curved; vein 3 from angle of cell; 4, 5 stalked; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 2 from angle of cell; 3 and 5 strongly stalked, 4 absent; 6, 7 shortly stalked ; 8 anastomosing with 7. 108 SIR GHORGE HAMPSON ON THE Srcr. I. (Commotria.) Antenne of male unipectinate, the apical part ciliated. (1) CoMMorRiA MESTELLA, sp. . Head and thorax purple-pink mixed with some whitish ; abdo- men pale fulvous yellow, ochreous white at base and extremity ; peetus, legs, and ventral surface of abdomen whitish tinged with purple. Fore wing’ purple-pink, the veins white defined on each side by fine brown streaks, the white on median nervure stronger and more strongly defined by black-brown below; a minute black- brown spot at upper angle of cell and point at lower angle. Hind wing whitish tinged with ochveous brown. Br. C. Arrica, Mt. Mlanje (Weave), 9 5d, 3 2 type.-. Hap. 20-22 mm. (2) CoMMOTRIA LATICOSTELLA. Commotria laticostella Hmpsn. Rom. Mém. vii. p. 343, pl. 52. f. 14 (1901). Brazit, Amazons. (3) CoMMOTRIA INVENUSTELLA. Commotria ivenustella Berg, An. Soc. Arg. xix. p. 278 (1885); Rag. Rom. Mém. vii. p. 343, pl. 36. f. 24. S. Brazin; ARGENTINA. (4) ComMorriA ARRHABDELLA, sp. 0. 2. Head and thorax pale red-brown ; abdomen whitish tinged with red-brown, dorsally fulvous yellow towards base; pectus and legs whitish tinged with red-brown. Fore wing pale flesh- red shghtly irrorated with dark scales; a terminal series of slight dark points. Peru, R. Pachaya, 192 type. Hap. 24 mm. Seor. II. (Tolima.) Antenne of male serrate. (5) *COMMOTRIA ROSEOPENNELLA. Volusia roseopennella Hulst, Trans. Am. Ent. Soc, xvii. p. 206 (1890); Rag. Rom. Mém. viii. p. 340, pl. 51. f. 3; Dyar, Cat. Lep. N. Am. p. 438. - U.S.A., Florida. (6) *COMMO?PRIA OBERTHURI. Tolima oberthurii Rag. Nouv. Gen. p. 41 (1888); id. Rom. Mem. vil. p. 341, pl. 38. f 4. CoLoMBIA. ; (7) *COMMOTRIA OPACELLA. Anerastia opacella Huist, Kut. Am. i. p. 138 (1887); Rag. Rom. .Mém. vin. p. 341, pl. 36. f. 23; Dyar, Cat. Lep. N. Am. p. 438. U.S.A., Texas. PYRALIDH, SUBFAMILY HYPSOTROPINA. 109 (8) rCOMMOTRIA PHYCITELLA. Tolima phycitella Rag. Nouv. Gen, p. 41 (1888); id. Rom. Mém. vill. p. 341, pl. 44. f. 17. © Gop Coast. Sect. III. (Mangala.) Antenne of male laminate and ciliated. (9) rComMOrRIA TRIPARTELLA, Sp. n. 2. Head and thorax purple-pink; abdomen white, dorsally tulvous yellow towards base ; pectus, leg&, and ventral surface of abdomen white tinged with purplish pink; anal tuft yellow below. Fore wing with white costal fascia narrowing to apex leaving the costal edge dark towards base, then pinkish, defined below by a dark reddish-brown fascia, the inner half of wing rose-pink, whiter towards inner margin. Hind wing white. N. Cuina, Pekin (Hughes), 1 9 type. Hap. 20 mm. (10) ¢ComMMorriA NEURIAS, sp. n. Head and thorax white suffused with red-brown; abdomen white, dorsally tinged with fulvous yellow towards base; pectus and legs white tinged with brown. Fore wing white tinged with reddish brown, the veins white defined on each side by slight dark brown streaks; the costal area defined below by a brown shade; obliquely placed almost medial dark brown points in submedian fold and on vein 1; a dark point just above lower angle of cell; obliquely placed postmedial dark points on veins 6 to 2 and in submedian fold and a point nearer the termen on vein 1; a terminal series of black points. Hind wing white slightly tinged with ochreous brown. N. Nigeria, Zungeru (Macfie), 1 $ ; Br. C. Arrica, Mt. Mlanje (Weave), 13.,12 type. Hap. 16 mm. (11) fComMMorrRIA ERYTHROGRAPTA, Sp. 0. ¢. Head and thorax white tinged with rufous; abdomen white tinged with ochreous yellow ; pectus and legs white mixed with red-brown. Fore wing white tinged with rufous, the veins’ and submedian fold white defined on each side by slight rufous streaks; the costal area defined below by a dark brown streak and a dark streak below basal half of median nervure; obliquely placed almost medial dark points below the cell and on vein 1; a dark point just above lower angle of cell and obliquely placed postmedial dark points on veins 6 to 2, Hind wing white with a slight ochreous tinge. Br. C. Arrica, Katungas (de Jersey), 1 5 type. Exp. 20 mm. (12) pCoMMOTRIA RUFIMEDIA, Sp. n. 3. Head and thorax white tinged with red-brown ; abdomen creamy white. Fore wing white faintly tinged with rufous and irrorated with fuscous; a rufous shade below median neryure ; 110 SIR GEORGE HAMPSON ON THE a minute antemedial black spot on vein 1 and minute discoidal spot; an oblique postmedial series of black points on veins 4 to 2 and a point on vein |; a terminal series of black points. Hind wing white tinged with ochreous. Br, C. Arrica, Mt. Mlanje (eave), 13 type. Hap. 16 mm. (13) fTCoMMOTRIA RHODONEURA, Sp. n. Q. Head and thorax rufous; abdomen whitish tinged with rufous; palpi whitish below ; fore legs red-brown ; mid and hind legs whitish tinged with rufous. Fore wing yellowish white, the veins streaked with purplish pink and the costal area suffused with purplish pink; a black antemedial point on vein 1, a discoidal point and postmedial points on veins 4, 2,1; a terminal series of black points. Hind wing white tinged with ochreous rufous. Transvaal, White R. (Cooke), 12 type. Hap. 20 mm. (14) pCoMMOTRIA RUFIDELINEATA, Sp. n. Head and thorax whitish suffused with rufous; abdomen creamy white, dorsally fulvous yellow towards base; pectus and legs white tinged with red-brown. Fore wing ochreous white, the veins defined on each side by fine rufous streaks, the costal area defined below by a slight rufous shade; two antemedial blackish points on vein | and obliquely placed postmedial points on veins 4 to 1; a terminal series of black points. Hind wing ochreous white. Br. EK. Arrica, Nairobi (Anderson), 1 2 type; Br. C. ArrRica, Mt. Mlanje (Weave), 1 5. Hap. 24 mm. (15) tComMorRIA MIOSTICTA, sp. n. 3. Head and thorax white tinged with rufous; abdomen creamy white, dorsally fulvous yellow towards base ; pectus, legs, and ventral surface of abdomen white suffused with brown. Fore wing white tinged with rufous, the veins white defined on each side by fine rufous streaks ; the costal edge blackish towards base ; the costal area defined below by a slight red-brown shade; a black point just above lower angle of cell. Hind wing white slightly tinged with ochreous. SrERRA LEONE (Clements), 15 type. Hap. 22 mm. (16) *ComMorRIA CRASSISCAPELLA. Mangala crassiscapella Rag. Nouv. Gen. p. 41 (1888) ; id. Rom. Mém. viii. p. 342, pl. 37. f. 17. _ SUDAN. (17) fCoMMOTRIA PHENICIAS, sp. n. ¢. Head and thorax whitish suffused with rufous; abdomen yellowish white; pectus and legs whitish suffused with brown. Fore wing white very thickly irrorated with deep purple-pink, PYRALIDH, SUBFAMILY HYPSOTROPINE. Bel the lower part of cell and the area just beyond it much whiter, the costa tinged with brown; a small black-brown discoidal spot 5 the veins towards termen with slight brown streaks. Hind wing yellowish white, the costa tinged with brown towards apex. N. Nigeria, Zungeru (Macfie), 1 3 ; Uaanpna, Katesa (Betton), 1g type. Hap. 20-22 mm. (18) TComMorRia ROSELLA, sp. n. Head and thorax bright rose-pink ; abdomen ochreous ; pectus whitish; legs and abdomen pink. Fore wing bright vose-pink mixed with some whitish except on costal area, the median nervure and veins beyond the cell with fine deep pink streaks; a small deep pink spot on upper discocellular ; cilia fuscous at apex. Hind wing pale ochreous, the costa and cilia at apex tinged with pink. Ab. 1. Fore wing with a dark reddish-brown shade along sub- eostai nervure and thence to apex, the spot on upper discocellular dark brown. Br. C. Arrica, Mt. Mlanje (Weave), 4 3, 52 type. Hap. 22-26 mm. (19) tComMorriA ALBINERVELLA, sp. 0. 9. Head and thorax pale purplish pink; abdomen ochreous white, dorsally fulvous yellow towards base; pectus, legs, and ventral surface of abdomen whitish tinged with pink, Fore wing pale purple-pink, the veins streaked with white ; the costal area white tinged with pink, narrowing to apex and defined below by a slight brown shade; a slight dark point at upper angle of cell. Hind wing white with a slight ochreous tinge. Ruopesia, Bulawayo (“yles), 12 type. Hap. 20 mm. (20) TComMMOrRIA VENOSELLA, sp. n. do. Head, thorax, and abdomen whitish suffused with rufous ; fore femora and tibie black-brown in front. Fore wing whitish suffused with purplish rufous and slightly irrorated with blackish in the interspaces; the veins prominently streaked with white. Hind wing ochreous whitish, with a shght reddish-brown terminal line except towards tornus. Br. C. Arrica, Mt. Mlanje (eave), 1 3 type. Hap. 30 mm. (21) fCoMMOTRIA RHODOCHROA, sp. n. 3. Head and thorax pale rose-pink; abdomen ochreous white, dorsally fulvous yellow towards base; pectus, legs, and ventral surface of abdomen whitish suffused with red-brown. Fore wing pale rose-pink, the costal area with a slight red-brown tinge; the veins streaked with white and defined on each side by fine deeper pink streaks. Hind wing ochreous white. Nata, Tugela R., Bonds’ Drift (Reynolds), Ig type. Hap: 26 mm. IY SIR GEORGE ILAMPSON ON THE (22) rCoMMOTRIA CASTANEIPARS, Sp. n. 2. Head, thorax, and abdomen deep red-brown ; hind tibize white towards base. Fore wing with narrow white costal fascia narrowing toa point before apex, the area below it deep chestnut- brown to median nervure and vein 2, the inner area purplish pink. Hind wing red-brown. Br. C. Arrica, Mt. Mlanje (Weave), 19 type. Hap. 22 mm. (23) TCOMMOTRIA PROPH ELLA, Sp. n. 2. Head and thorax pale flesh-red ; abdomen ochreous ;_ palpi tinged with brown; pectus and legs whitish suffused with brown. Fore wing pale flesh-red, the costal area broadly suffused with brown, extending on basal half to median nervure; the veins beyond the cell finely streaked with brown. Hind wing ochreous white. Br. C. Arrica, Mt. Mlanje (Weave), 19 type. ° Hap. 22 mm. (24) TCoMMOTRIA PHLEBICELLA, Sp. n. @. Head and thorax pale flesh-pink mixed with some whitish ; abdomen whitish, dorsally tinged with fulvous-yellow towards base ; pectus, legs, and ventral surface of abdomen white tinged with brown. Fore wing pale flesh-pink, the costal area broadly suffused with brown, extending to the median nervure towards base ; the costal edge and veins finely streaked with white. Hind wing ochreous. white. MASHONALAND, Salisbury (J/arshall), 29 type. Hap. 26 mm. (25) +CoMMOTRIA ENERVELLA, Sp. Nn. 3S. Head and thorax whitish suffused with pale flesh-red ; abdomen ochreous white. Fore wing whitish suffused with pale purplish pink and the costal half tinged with brown ; the veins, except on inner area, streaked with white and. defined on each side by fine brown streaks. Hind wing white tinged with brown except towards base and inner margin Formosa, Takow (Wileman), 1 S$ type. Hap. 18 mm. Genus SIBoGa. Type. Siboga Hmpsn. Rom. Mém, viii. p. 338 (1901)......... JSalsella. Proboscis aborted and minute; palpi upturned, the 2nd joint reaching to vertex of head and hollowed out to receive the brush- like maxillary palpi, the 3rd joint moderate and porrect; frons with conical prominence ; antennz of male typically serrate and ciliated, the basal joint elongate, the shaft with double ridge of scales at base above enclosing a hollow. Fore wing long and narrow, the apex rounded, the termen obliquely curved ; vein 3 from close to augle of cell; 4, 5 strongly stalked; 6 front below upper angle; 8, 9, 10 stalked; 11 from cell, Hind wing with PYRALID#, SUBFAMILY HYPSOTROPINA. 113 vein 2 from well before angle of cell; 3 and 5 stalked, 4 absent ; 6, 7 shortly stalked; 8 not anastomosing with 7. Sect. I. Antenne of male unipectinate with moderate branches, the apical part ciliated. (1) StBoGA ALBIMEDIELLA, Sp. n. Head and thorax white tinged with pink and brown; abdomen ochreous, the first three segments ochreous on dorsum. Fore wing pale pink, the veins streaked with white; the costal area tinged with brown; a white fascia from base to termen above . median nervure and vein 5. Hind wing white slightly tinged with ochreous especially towards termen. PoungaB, Simla, 1g type. Haep.26mm. ~* \ Sror. IT. (Siboga.) Antenne of male serrate and ciliated. (2) *Srpoga FALSELLA. © Hypsotropha falsella Snell. Midden-Sumatra Lep. p. 82 (1880) ; Rag. Rom. Mém. viii. p. 338, pl. 38. f. 3. SUMATRA, Sect. IIJ. Antennze of male laminate and almost simple. (3) TS1BOGA DIALEUCELLA, Sp. n. 3. Head and thorax white, suffused with rufous except on vertex of head and dorsum of thorax; abdomen creamy white, dorsally fulvous yellow towards base; palpi white in front; pectus and legs white slightly tinged with red-brown. Fore wing white suffused with rufous; the veins white defined on each side by fine rufous streaks, the median nervure defined below by a rufous fascia ; a White fascia through the cell, then narrower along discal fold to termen. Hind wing ochreous white. Kasumir, Goorais Valley (Leech), 13 type. Hap. 24 mm. (4) TSIBOGA ZEAVORA, sp. n. @. Head, thorax, and abdomen whitish suffused with rufous, the last dorsally fulvous yellow towards base. Fore wing whitish tinged with rufous, the veins defined on each side by streaks formed of red-brown scales, the cell with two streaks in it; the inner margin irrorated with red-brown ; a terminal series of prominent black points. Hind wing ochreous white with a terminal series of brown striz except towards tornus. Matay Srates, 1 2 type. Hap. 30 mm. Larva feeds on maize. Proc. Zoou. Soc.—1918, No. VIII. 8 114 STR GEORGE HAMPSON ON THE Genus EMATHEUDES. Type. Ematheudes Zell. Stett. Ent. Zeit. 1867, p. 385 ... punctella. Proboscis aborted and minute; palpi downcurved, extending about three times length of head and thickly scaled; maxillary palpi minute and filiform; frons with large tuft of scales ; antenns of male minutely serrate and ciliated. Fore wing narrow, the apex rounded, the termen evenly curved; vein 3 from close to angle of cell; 4,5 stalked; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 2 from well before angle of cell; 3 and 5 stalked, 4 absent; 6, 7 shortly stalked ; 8 not anastomosing with 7. (1) Emarngupes PUNCTELLA. Chilo ‘punctella Treit. Schmett. Eur. ix. 2, p. 268 (1833); Dup. Lép. Fr. pl. 273. f. 4; Herr.-Schiff. Kur. Schmett: iv. p. 108, Mine 18515) Rag.) Rome "Mém. viii. p. 333; Staud. Cat. Lep. pal. itt; [Os dha}, S. France; Spain; Corsica; Iraty; Sicity; Morocco ; GREECE ; TurKEY ; Cyprus; Asta Mrnor; Syria. (2) *EMATHEUDES PSEUDOPUNCTELLA. Hmatheudes pseudopunctella Rag. Nouv. Gen. p. 40 (1888) ; id. Rom. Mém. viii. p. 334, pl. 36. f. 22 : Staud. Cat. lise pal. 11. p. 13. Syria. Probably an aberration of 1. punctella: (3) EMATHEUDES STRAMINELLA. Hmatheudes straminella Snell, Tijd. v. Ent. 1872, p. 107, pl. 8. ig Oh GAMBIA; STERRA LeonE; ANcotA; Br. C. Arrica; Portu- GuUESE K. AFRICA. (4) 7TEMATHEUDES LENTISTRIGALIS. Hnmatheudes lentistrigalis Hmpsn. Tr. Zool. Soc. xix. p. 134, pl. iv. f. 65 (1909). Goup Coast; N. NIGERIA: Br. EH. eee UGANDA: Br. C. AFRICA. (5) EMATHEUDES PALEATELLA. Ematheudes puleatella Rag. Nouv. Gen. p. 40 (1888); id. Rom. Mém. viii. p. 334, pl. 36. f. 20. Br. E. ArricA; Ucanpa; Br. C. Arrica; MASHONALAND ; TransvAAL; Navau; BasuToLAND; CAPE CoLoNy. (6) EMATHEUDES TUNESIELLA. Ematheudes tunesiella Rag. Iris, v. p. 298 (1892); id. Rom. Mém. vii. p. 335, pl. 42. f. 22; Staud. Cat. Lep. pal. ii. p. 13. S. Iraty; Tunis; Syria; W. TurkEsran, PYRALIDZ, SUBFAMILY HYPSOTROPIN &. 115 (7) EMATHEUDES CRASSINOTELLA. Ematheudes crassinotella Rag. Nouv. Gen. p. 41 (1888); id. Rom, Mém. viii. p. 335, pl. 35. f. 26. ZanziBAR; Br. BE. ArricA; MASHONALAND; NATAL. (8) *EMATHEUDES VARICELLA. Ematheudes varicella Rag. Ann. Soc. Ent. Fr. 1887, p. 258 ; id. Rom. Mém. viii. p. 336, pl. 35. f. 27; Staud. Cat. Lep. pal. ie Pals: ARMENIA; W. TURKESTAN. (9) *EMATHEUDES VITELLINELLA. Ematheudes vitellinella Rag. Ann. Soc. Ent. Fr. 1887, p. 258; id. Rom. Mém. viii. p. 336, pl. 49. f. 22; Staud. Cat. Lep. pal. il. p. 13. Asta Minor, Georgia. (10) *KMarHEUDES EUCHLYTELLA,. Ematheudes euchlytella Rag. Nouv. Gen. p. 41 (1888); id. Rom. Mém. viii. p. 387, pl. 36. f. 21. ARGENTINA. Genus Brapra. anh Type. Biafra Rag, Nouv. Gen. p. 40 (1888)............... concinnella. Proboscis aborted and minute ; palpi downcurved, extending about three times length of head and moderately scaled; maxil- lary palpi slightly dilated with scales ; frons smooth, with large pointed tuft of hair; antenne of male minutely serrate and ciliated, the basal joint rather long, the shaft with double ridge of scales at base enclosing a hollow. Fore wing very narrow, the apex rounded, the termen obliquely curved ; vein 3 from near angle of cell; 4, 5 separate ; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 2 from near angle of cell; 3 and 5 stalked, 4 absent; 6, 7 shortly stalked; 8 anas- tomosing with 7. (1) BraFrRA CONCINNELLA. Biafra concinnella Rag. Nouv. Gen. p. 40 (1888); id. Rom. Mém. viii. p. 330, pl. 38. f. 2. . N. Nigeria; Br, C. Arrica; MAsHonaLaANd; TRANSVAAL; Natal. (2) FBIAFRA RHODINELLA. Biafra rhodinella Rag. Nouv. Gen. p. 40 (1888); id. Rom. Mém. viii. p. 381, pl. 44. f. 20. Goup Coast; N, Nigeria; MasHonaLtanp; TRANSVAAL. 8* 116 SIR GEORGE HAMPSON ON THE Genus Erurorropa, nov. Type, #. pyromerella. Proboscis aborted and minute; palpi porrect and _ slightly downcurved, extending about twice the length of head, the 2nd joint fringed with rough scales below, the 3rd moderate ; maxil- lary palpi strongly dilated with scales; frons smooth, with pointed tuft of hair above; antenne of male somewhat laminate and minutely ciliated, the basal joint long, the shaft with ridge of scales above at base. Fore wing long and very narrow, the apex rounded, the termen obliquely curved; veins 3, 4 stalked on one side of the specimen from a point on the other; 5 sepa- rate; 6 from below upper angle; 8, 10, 11 stalked, 9 absent. Hind wing with vein 2 from well before angle of cell; 3 and 5 from angle and approximated for some distance, 4 absent; 6, 7 shortly stalked ; 8 anastomosing with 7. ETHIOTROPA PYROMERELLA, Sp. Nn. 3. Head, tegule, and base of patagia fiery red, the rest of thorax brownish ochreous; abdomen ochreous white, dorsally fulvous yellow towards base; pectus, legs, and ventral surface of abdomen whitish suffused with brown. Fore wing with whitish costal fascia narrowing to apex, the costal edge fiery red to beyond middle, defined below by a black-brown fascia ; the rest of wing fiery red. Hind wing white tinged with ochreous brown. . N. Nigeria, Akassa (Zugard), 1 ¢ type. Hap. 22 mm. Genus BAproTRoPa, nov. Type, B. tricolorella. Proboscis aborted and minute; palpi porrect and slightly downcurved, extending about three times length of head, the 2nd joint fringed with rough scales above, the 3rd moderate ; maxillary palpi minute and filiform; frons smooth and rounded, without tuft of hair; antennz of male strongly uniserrate, the basal joint long, the shaft with double ridge of scales at base enclosing a hollow. Fore wing narrow, the apex rounded, the termen evenly curved; vein 3 from before angle of cell; 4, 5 from angle; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 2 from well before angle of cell; 3 and 5 from angle, 4 absent; 6, 7 shortly stalked; 8 anastomosing with 7. +BAPTOTROPA TRICOLORELLA. Patna tricolorella Hmpsn. J. Bomb. N. H. Soe. xii, p. 308 (1899); Rag. Rom. Mém, vii. p. 340, pl. 52. f. 15, Assam, Khasis. PYRALIDH, SUBFAMILY HYPSOTROPIN2. 117 Genus PATNA. Type. Paina Rag. Nouv. Gen. p. 39 (1888)............... eboricostella. Proboscis absent ; palpi porrect and almost straight, extending about three times length of head, the 2nd joint slightly fringed with hair above towards extremity, the 3rd moderate ; maxillary palpi small and filiform; frons smooth and rounded, without tuft of hair; antenne of female almost simple. Fore wing rather narrow, the costa typically almost straight, the apex rounded, the termen evenly curved; vein 3 from near angle of cell; 4,5 from angle and approximated for a short distance; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 2 from well before angle of cell; 3 and 5 from angle, 4 absent; 6, 7 from upper angle; 8 not anastomosing with 7. (1) PaTNA EBORICOSTELLA. Patna eboricostella Rag. Nouv. Gen. p. 39 (1888); Hmpsn. Moths Ind. iv. p. 57; Rag. Rom. Mém. viii. p. 330, pl. 38. f. 1. ) SIKHIM; BHUTAN. (2) PATNA VENATELLA, sp. 0, 2. Head and thorax pale rufous ; palpi whitish except above ; pectus, legs, and abdomen whitish tinged with red-brown. Fore wing white, the veins, discal fold in the cell and the submedian fold defined by fine purplish-pink streaks; a minute dark brown spot just above lower angle of cell; a ‘yararaginell series of black points. Hind wing white ‘slightly tinged with ochreous. Br. E. Arrica, Tagas (etton), 1 2, Aios (Betton), 1 2 type. Hep. 32 mm. (3) TPATNA BRUNNEICOSTELLA, Sp. n. @. Head and thorax pale flesh-pink; abdomen ochreous white; palpi, pectus, legs, and ventral surface of abdomen whitish suffused with red-brown. Fore wing white, the costal area tinged with brown, the area below the cell and vein 2 suffused saith pale pink; the veins white, those beyond the cell defined on each side by fine pink streaks, the median nervure and vein 2 defined below by stronger streaks; a dark point in lower angle of cell. Hind wing ochreous white, Transvaal, White R. (C ‘ooke), 1 9 type. Hap. 32 mm. Genus MEGALOPHOTA, nov. Type, J. leonelta. Proboscis absent; palpi obliquely upturned, the 2nd joint reaching .to above vertex of head, dilated and hollowed out to receive the brush-like maxillary palpi, the 3rd minute ; frons 118 SIR GEORGE HAMPSON ON THE with long truncate conical prominence; antenn of male pecti- nate with rather long uniseriate branches to near apex, the shaft with large sinus at base containing a double ridge of scales enclosing a hollow. Fore wing rather long and narrow, the apex rounded, the termen evenly curved; vein 2 from well before angle of cell; 3 from before angle; 4, 5 from angle; 6 from below upper angle; 8, 9 stalked; 10, 11 from cell. Hind wing with vein 2 from well before angle of cell; 3 and 5 stalked, 4 absent ; 6, 7 shortly stalked ; 8 not anastomosing with 7. MEGALOPHOTA LEONELLA, Sp. Nn. 3. Head and thorax ochreous white with a slight red-brown tinge on shoulders, the antennal tufts. black on inner side; abdomen ochreous ; pectus and legs ochreous white tinged with - red-brown. Fore wing ochreous white irrorated with brown, the costal avea slightly irrorated to near apex, Hind wing ochreous white. SIERRA LEONE (Dudgeon), 1 g type. Hap. 20 mm. Genus MARTIA. Type. Mortia Bag. N. Am: Rhye: p: 18 (887)... a... arizonella. Urula Hulst, Can. Ent. xxxu. p. 175 (1900) ...... arizonella. Proboscis absent ; palpi with the 2nd joint porrect, extending about twice the length of head, the 3rd rather oblique, long, slender, and somewhat acute at extremity; maxillary palpi slight and filiform; frons with large truncate conical prominence; antenne of male minutely serrate and with fascicles of long cilia. Fore wing rather narrow, the apex rounded, the termen evenly curved ; vein 2 from long before angle of cell; 3 from before angle; 5 from above angle; 6 from below upper angle; 8, 9 stalked; 10, 11 from cell. Hind wing with vein 2 from long before angle of cell; 3 and 5 from angle, approximated for a short distance, 4 absent ; 6, 7 from upper angle; 8 not anasto- mosing with 7. MARIA ARIZONELLA. Martia arizonella Rag. N. Am. Phye. p. 18 (1887); id. Rom. Mém. viii. p. 367, pl. 38. f. 20; Dyar, Cat. Lep. N. Am. p. 439, Orula incongruela Hulst, Can. Ent. xxxul. p. 175 (1900); Dyar, Cat. Lep. N. Am. p. 437. U.S.A., Colorado, Arizona. Genus D1scorRONTIA, Type. Discofrontia Hmysn. Rom. Mém. viii. p. 350 (1901). normella. Proboscis aborted and minute; palpi upturned, the 2nd joint reaching to vertex of head and moderately scaled and flattened, PYRALID®, SUBFAMILY HYPSOTROPIN®. 119 the 3rd moderate; maxillary palpi slight and filiform; frons broad, with a disk of concentric white scales converging to middle; antenne of male strongly serrate, with a large sinus andl ridge of scales at base of shaft. Fore wing rather narrow, the apex rounded, the termen evenly curved;.vem 2 from well before angle of cell; 3 from before angle; 4,5 from angle: 6 from below upper angle; 8, 9 stalked; 16, ii om cell. Hind wing with vein 2 from before angle of wail ; 3 and 5 frem angle, 4 absent; 6, 7 from upper angle; 8 not anastomosing with 7. * DISCOFRONTIA NORMELLA. Discofrontia normella Hmpsn. Rom. Mém. vii. p. 350, pl. 52. f. 20 (1901). NATAL. Genus CRITONIA, ‘ Type. Critonia Rag. Bull. Soc. Ent. Fr. 1890, p. cexiv. sulteenetonella Singhalia Hmpsn. J. Bomb. Nat. Hist. Soc. xii. p. 309 (1898); id. Rom. Meém. vii. p. 351 (CNS LU is esi ea a oer a a, SRE aceon sarcoglauca. Proboscis aborted and minute; palpi typically downcurved, extending about three times length of head and moderately sealed; maxillary palpi small and filiform; frons smooth and with slight tuft of hair; antennz of male typically serrate and fasciculate, the shaft with sinus at base containing a large ridge of scales. Fore wing rather long and narrow, the apex ronatieds the termen evenly curved; vein 3 from before angle of cell; 4, 5 from just above angle; 6 from below upper angle; 8, 9 stalked ; 10, 11 from cell, 10 approximated to 8,9. Hind wing with veins 3 and 5 from angle of cell and approximated for a short distance, 4 absent; 6, 7 shortly stalked ; 8 not anastomos- ing with 7. Sect. I. Palpi of male obliquely upturned, the 2nd joint hollowed out to receive the brush-like maxillary palpi, the 3rd short; antennze laminate, with large sinus and ridge of scales at base of shaft. (1) }CRrrironIA PHHONEURA, Sp. n. do. Head and thorax whitish suffused with red-brown ; abdo- men ochreous white, dorsally fulvous yellow towards base ; pectus and legs whitish tinged with brown. I’ore wing whitish tinged with red-brown, the veins except on inner area blackish defined on each side by fine white streaks ; the costal area white, narrowing to apex and defined below by a red-brown shade, the costal.edge brown to beyond middle and the veins on costal area finely streaked with black; a minute antemedial black spot on vein 1, a point at middle of submedian fold and minute post- medial streaks above vein 2 and on vein 1 ; cilia flesh-white with 120 SIR GEORGE HAMPSON ON THE series of minute black streaks near base except towards tornus. Hind wing whitish tinged with brown especially on costal area and at termen. Formosa, Banshorio (Wileman), 1 3 type. Hap. 18 mm. (2) TCRITONIA PROMELENA. Critonia promeena Hmpsn. J. Bomb. Nat. Hist. Soe. xii. p- 309 (1898); id. Rom. Mém. viii. p. 366, pl. 51. f. 23. SIKHIM, a (3) TCRITONIA PURPUREOTINCTA. Critonia purpureotincta Hmpsn. Moths Ind. iv. p. 61 (1896) ; id. Rom. Mém. viii. p. 365, pl. 51. f. 22. SIKHIM; Buuvin. (4) fCrivoNIA HOLORHODA. Critonia holorhoda Hmpsn. J. Bomb, Nat. Hist. Soc. xviii. p- 259 (1908). CEYLON. Secr. I]. Maxillary palpi of male filiform. A. (Critonia). Antenne of male serrate, with larger sinus and ridge of scales at base of shaft; palpi downcurved and about three times length of head. (5) *CRITONIA SUBCONCINNELLA. Critonia subconcinnella Rag. Bull. Soc. Ent. Fr. 1890, p. cexiv ; id. Rom. Mem. viii. p. 365, pl. 6. f. 20. BurMA. (6) TCRITONIA LEUCOPLEURA, Sp. n. gd. Head and thorax whitish suffused with purplish pink; abdomen whitish suffused with ochreous brown ; antenne with the tuft blackish; palpi, pectus, and legs whitish tinged with brown. Fore wing whitish suffused with purplish pink, the veins streaked with blackish, vein 1 only towards termen ; the costal area pure white, narrowing to apex and defined below by a blackish shade; the costal edge dark to beyond middle and the. interspaces of terminal area with slight dark streaks except towards tornus. Hind wing whitish, the costal area broadly suffused with brown. BasuToLanD, Maseru (Crawshay), 1 3 type. Hap. 26 mm. (7) +CRITONIA ROSEISTRIGELLA. Critonia roseistrigella Hmpsn. Moths Ind. iv. p- 61 (1896) ; id. Rom. Mém. viii. p. 365, pl. 51. f. 21. Mapras, Nilgiris ; Puinippines, Luzon. 4 CY PYRALIDH, SUBFAMILY HYPSOTROPINA. 121 (8) CRITONIA OCHRACEALIS. Critonia ochracealis Hmpsn. J. Bomb. Nat! Hist. Soch xx p. 1251 (1912). PungaB, Kangra; MaApras, Nilgiris. (9) *CRITONIA HILGERTI. Pectinigeria hilgertti Roths. Nov. Zool. xxi. p. 236. ALGERIA. B. Antennze of male laminate and without sinus and ridge of scales at base of shaft. a. (Singhalia.) Palpi of male with the 2nd joint obliquely upturned to vertex of head and thickly scaled, the 3rd porrect, long and blunt. (10) TCrITONTA SARCOGLAUCA. Critomia sarcoglauca Hmpsn. Moths Ind. iv. p. 60 (1896); id. Rom. Mém. viii. p. 351, pl. 51. f. 24. CEYLON. 6. Palpi of male downcurved and extending about three times length of head. (11) Crrronta RHODESSA. Saluria rhodesso Turner, Pr. R. Soc. Queens]. xviii. p. 120 (1903). (QUEENSLAND. (12) TCRITONIA SARCOIDA, Sp. Nn. Head and thorax purplish pink, the head and shoulders tinged with brown; abdomen ochreous white, dorsally fulvous yellow towards base ; pectus, legs, and ventral surface of abdo- men ochreous tinged with brown. Fore wing purplish pink, the costal area tinged with brown; the veins, discal fold in the cell, and submedian fold white defined on each side by fine purplish- pink streaks, the median nervure rather more strongly streaked with white and with a brown streak below it. Hind wing ochreous white, the costal area tinged with brown. Br. E. Arrica, Njora (Cholmley), 1 6; Br. C. Arrica, Mt. Mlanje (Weave), 3 2 ; Porrucurse HK. Arrica, Kola Valley (Weave), 3 2 ; MasHoNALAND, Salisbury (/arshall), 1 2 ; TRans- VAAL (Pead), 1 ¢ type. Hap. 28-34 min. Genus MonocrENocERA. + Type. Monoctenocera Hmpsn. J. Bomb. Nat. Hist. Soc. x11. p- 310 (1898) ; id. Rom. Mém. viii. p. 311(1901). brachiella. Proboscis aborted and minute; palpi obliquely upturned, the 2nd joint reaching to just above vertex of head and hollowed out to receive the brush-like maxillary palpi, the 3rd short and 22 SIR GEORGE HAMPSON ON THE thickly sealed ; frons smooth, with large tuft of hair; antennze of male unipectinate, typically with very short branches, the apical part serrate, the shaft with large sinus and ridge of scales at base; mid and hind tibi typically fringed with long hair. Fore wing narrow, the apex rounded, the termen evenly curved ; vein 3 from close to angle of cell; 4, 5 strongly stalked ; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 3 closely approximated to 4+, 5 for some distance ; 4, 5 strongly stalked; 6, 7 shortly stalked; 8 anastomosing with 7. Sect. I. Antenne of male with the branches long; mid tibize fringed with hair at base only, the hind tibiz at extremity only. (1) MonocrenocEeRA LEUCANIA. Catagela leucania Feld, Reis. Nov. pl. 137. f. 13 (1874); Hmpsn. Moths Ind. iv. p. 63; id. Rom. Mem. viii. p. 312, pl. 51. fae: Hab. Mavras, Nilgivis; TRAVANCORE; CEYLON. Secr. II. Antenne of male with short branches towards base, then serrate: mid and hind tibie fringed with long hair throughout. (2) MonocTrENOCERA BRACHTELLA. Polyocha brachiella Hmpsn. J. Bomb. Nat. Hist. Soc. xii. p. 310 (1898) ; id. Rom. Mem. viii. p. 312, pl. 36. f. 6 Hab. StKkKIM; Bevxcar, Calcutta; Borneo. Genus SABORMA. Type. Saborma Rag. Nouv. Gen. p. 37 (1887) ............ forcipella. Proboscis aborted, minute; palpi of male upturned to about vertex of head, slender, typically hollowed out to contain the brush-like maxillary palpi; frons smooth; antenne of male typically strongly serrate, with sinus and large double ridge of scales at base. Fore wing narrow, the apex rounded, the termen evenly curved ; vein 3 from close to angle of cell; 4, 5 strongly stalked; 6 from below upper angle; 8, 9, 10 stalked; 11 from cell. Hind wing with vein 3 approximated for some distance to 4, 5 which are strongly stalked; 6, 7 shortly stalked; 8 not anastomosing with 7. Secr. I. Palpi of male with the 2nd jomt hollowed out to receive the brush-like maxillary palpi; antenne serrate. (1) *SaBoRMaA FORCIPELLA. Saborma forcipella Rag. Nouv. Gen. p. 37 (1888); id. Rom. Mém. viii. p. 310, pl. 35. f. 22. SUMATRA. PYRALID#®, SUBFAMILY HYPSOTROPIN &. 123 (2) *SABORMA VICINA. Anerastia vicina Saalm. Ber. Senck. Ges. 1879, p. 307; id. Lep. Madag. p. 511; Rag. Rom. Mém. viii. p. 309, pl. 42. £..21. MADAGASCAR. Secr. II. Maxillary palpi of male filiform; antenne laminate and ciliated. (3) TSABORMA PAPUACOLA, sp. n. 3. Head and thorax whitish tinged with red-brown ; abdomen whitish tinged with brown, dorsally fulvous yellow towards base ; antennz with the tuft blackish on inner side; pectus and legs whitish tinged with brown. Fore wing white tinged with ochreous brown, the veins, discal fold in ene cell, and the sub- median fold white defined on each side by streaks formed of blackish scales; a terminal series of black points. Hind wing ochreous white with terminal series of dark points and strie. .Durcn N. Guinea, Mimika R. (Wollaston), 3 3 type. Hap. 26-30 mm. Genus OsactA. 4 Type Osakia Rag. Rom. Mém. viii. p. 318 (1901) ......... Tiere ite Proboscis aborted and minute; palpi obliquely upturned to about vertex of head, moderately scaled; maxillary palpi each a minute brush of scales; frons smooth and rounded; antennee of male ciliated, the shaft with sinus and double ridge of scales at hase; tibie fringed with hair. Fore wing ee) EAONY, the apex rounded, the termen evenly curved; veins 2 and 3 stalked from before angle of cell; 4, 5 separate ; 6 from below upper angle; 8, 9 staiked; 10, 11 from cell. Hind wing with vein 3 from angle of cell ; 4 and ) strong gly stalked ; 6,7 strong gly stalked ; 8 not anastomosing with 7. *OSACIA LINEOLELLA. Osakia lineolella Rag. Rom. Mém. viii. p. 319; pl. 43. f. 21 (OOD. JAPAN. Genus RAGonorta. Type. Ciris Rag. N. Am. Phye. p. 17 (1887), nec -Grote, Lep. SS SR eR ET Gh SENG ATE RAR Aer dotalis. Ragonotia Grote, Can. Ent. xx. p. 75 (1888)............ dotalis. Proboscis aborted and minute; palpi downturned, about three times length of head and rather broadly fringed with scales below; maxillary palpi filiform; frons with small rounded pro- minence with corneous plate below it; antennz of male ciliated, the basal joint large. Fore wing long and narrow, the apex rounded, the termen obliquely curved : vein 2 from towards angle of cell; 3 and 5 from close to angle ; 6 from below upper 124 SIR GEORGE HAMPSON ON THE angle; 8, 9 stalked; 10,11 from cell. Hind wing with vein 2 from close to angle of cell; 3 approximated for some distance to 4, 5 which are strongly stalked, or 4 rarely absent ; 6, 7 stalked; 8 not anastomosing with 7. RAGONOTTA DOTALIS. Anerastia dotalis Hulst, Trans. Am. Ent. Soe. xiii. p. 164 (1886) ; Rag. Rom. Mém. viii. p. 329, pl. 38. f. 19; Dyar, Cat. Lep. N. Am. p. 437. Ciris discigerella Rag. N. Am. Phye. p. 17 (1887). U.S.A., Colorado, Arizona. Genus PotyocHa. Tene Polyocha Zeller, Isis, 1848, p. 876............... sanguinariella. Polyochodes Chretien, Bull. Soc. Ent. Fr. 1911, Pesan conus aucceetey Gi Aseaee Santora aiaa Meee or erie stipella. . Proboscis aborted and minute; palpi typically downcurved, extending about three times length. of head, the 2nd joint moderately scaled, the 3rd rather long and naked; maxillary palpi dilated with scales; frons smooth, with tuft of scales ; antennee of male typically laminate and without sinus and ridge of seales at base. Fore wing long and narrow, the apex omnia the termen obliquely Curved ; vein 3 from close to angle of cell; 4, 5 strongly stalked; 6 from below upper angle; 8, 9 stalked; 10, 11 from cell. Hind wing with vein 2 from close to angle of cell ; 3 approximated for some distance to 4,5 which are strongly stalked ; 6, 7 shortly stalked ; 8 not anastomosing with 7. Secor. I. Palpi of male obtauely upturned ; antennee serrate, with sinus and ridge of scales at base of shaft. (1) +Ponyoona PLINTHOCHROA, sp. n.. Head and thorax bright rufous mixed with some ochreous ; abdomen ochreous, dorsally fulvous yellow towards base; antennz ochreous, Fore wing bright rufous with a faint purplish gloss, some ochreous in lower part of cell and below and just beyond the cell, the veins remaining rufous; a narrow yellowish-white costal fascia, tapering toa ‘point just before apex. Hind wing ochreous white, the costal area and termen tinged with ved- brown. TRANSVAAL, Karina (Cooke), 1 3 type, White R. (Cooke), 1 @. Hep. 26 mm. (2) TPoLYocHA LEUCOPLEURELLA. Emmalocera leucopleurella Rag. Nouv. Gen. p. 38 (1888) ; Rom. Mém. viii. p. 317, pl. 44. f. 15 Gop Coasr; 8. & a NIGERIA ; Kactarn ; Mapras. PYRALIDH, SUBFAMILY MYPSOTROPIN&. 125 (3) TPoLYOCHA GENSANALIS. Emmalocera gensanalis South, Trans. Ent. Soc. 1901, p. 405, pl: xiv. £. 30: CorREA. £ Src. II. Palpi of male downcurved ; antennze without sinus and ridge of scales at base of shaft. A. (Polyochodes). Antenne of male pectinate with uniseriate branches. (4) *PoLyYOCHA STIPELLA. Polyochodes stipella Chretien, Bull. Soc. Ent. Fr. 1911, p. 13. ALGERIA. B. (Polyocha). Antenne of male laminate. (5) tPoLyocuaA CINERELLA. Polyocha cinerella Hmpsn. Moths Ind. iv. p. 62 (1896); id. Rom. Mem. viii. p. 328, pl. 55. f. 4. PunsaB; BENGAL. (6) PoLyocHaA VENOSA, Epischnia venosa Zell. Isis, 1847; p. 31; Herr.-Schiiff. Schmett. Eur. iv. p. 109; Rag. Rom. Mém. viii. p. 327; Staud: Cat. Lep. pal. 1. p. 13. Cyprus; SYRIA. (7) PoLYocHA SANGUINARIELLA. Polyocha sanguinariella Zell. Isis, 1848, p. 876; Rag. Rom. Mem: viii. p. 327, pl. 8. f. 20. Br. C. ArricaA; MASHONALAND; TRANSVAAL; MADAGASCAR. (8) PoLyocHA VESCULELLA. Polyocha vesculella Rag. Nouv. Gen. p. 39 (1888); id. Rom. Mem. viii. p. 323, pl. 36: f. 11; Hmpsn. Moths Ind. iv. p. 63. Mapras, Palni Hills; TRAVANCORE. (9) *PoLyocHA FLAGRANTELLA. _ Polyocha flagrantella Rag. Rom. Mem. viii, p. 323, pl. 44. f. 24 (1901). MADAGASCAR. (10) tPoLyocHA STRIGIVENELLA. Polyocha strigivenella Hmpsn. J. Bomb, Nat. Hist. Soc. xii. p. 310 (1898) ; id. Rom. Mém. viii. p. 322, pl. 51. f. 19. Burma, 126 SIR GEORGE HAMPSON ON THE (11) *PotyocHa NEUROPTERELLA. Polyocha neuropterella Rag. Ann. Soc. Ent. Fr. 1887, p. 258 ; id. Rom. Mém. viii. p. 322, pl. 35. f. 23; Staud. Cat. Lep. pal. ii. p. 138. W. 'TURKESTAN. (12) *PoLyocHa FOUCART]. Polyocha foucarti Rag. Ann. Soc. Ent. Fr. 1887, p. 258; id. Rom. Mém. viii. p. 322, pl. 35. f. 24; Staud. Cat. Lep. pal. 11. p. 13. ALGERIA. (13) }PoLyocHa ACHROMATELLA, sp. n. ®. Head and thorax white tinged with ochreous ; abdomen white, dorsally fulvous yellow towards base; pectus and legs ochreous white. Fore wing pale ochreous, the veins white, less distinctly so on costal area. Hind wing white. N.S. Wates, Broken Hill (Lower), 3 9 type. Hap. 28 mm. (14) *PoLyocHA DETRITELLA. Polyocha detritella Rag. Nouv. Gen. p. 39 (1888); id. Rom. Mem. viii. p. 326, pl. 36. f. 14; Hmpsn. Moths Ind. iv. p. 63. PUNJAB: (15) 7PPoLyOCcHA FUSCICOSTELLA, sp. n. ©. Head and thorax glossy fuscous brown ; abdomen fuscous brown, pale red-brown at sides and extremity ; pectus and legs pale red-brown, the tarsi fuscous brown. Fore wing pale red-brown, the costal area broadly glossy fuscous brown and the inner basal area tinged with fuscous brown. Hind wing ochreous white, the costal area tinged with brown. Uf Nicn rar Toy N. Niceria, Zungeru (Jacfie), 2 2 type. Hap. 24 mm. Genus EMMALOCERA. : Type. EHmmalocera Rag. Nouv. Gen. p. 38 (1888)...... lewcocineta. Lodiana Rag. Nouv. Gen. p. 38 (1888) ......... umbrivittella. Papua Rag. Bull. Soc. Ent. Fr. 1889, p. cexx... latilimbella. Proboscis aborted and minute ; palpi of male typically obliquely upturned to above vertex of head, the 2nd joint hollowed out to receive the brush-like maxillary palpi, the 3rd short and porrect; frons smooth, obliquely flattened; antennz of male typically with short uniseriate branches, the basal joint large, the shaft with large sinus and ridge of scales at base. Fore wing rather long and narrow, the apex rounded, the termen evenly curved ; vein 3 from near angle of cell, 5 from just above angle; 6 from below upper angle; 8, 9 stalked; 10, 11 from cell, Hind wing PYRALIDH, SUBFAMILY HYPSOTROPIN®. 127 with vein 2 from well before angle of cell; 3 approximated for some distance to 4,5 which are strongly stalked; 6, 7 shortly stalked ; 8 not anastomosing with 7. Srct. I. Palpi of male upturned, the 2nd joint hollowed out to receive the brush- like maxillary palpi; antenne with sinus and ridge of scales at base of shaft. A, Antenne of male with rather long uniseriate branches. (1) rEMMALOCERA ORNATELLA, Polyocha ornatella Hmpsn. J. Bomb, Nat. Hist. Soc. xv. p. 21 (1903). PUNJAB. (2) ;EMMALOCERA PULVEREALIS. Polyocha pulverealis Hmpsn. J. Bomb. Nat. Hist. Soe. xv. p- 20 (1903). " Assam. (3) THMMALOCERA ENDOPYRELLA, Sp. n. 3. Head ochreous tinged with purplish pink, the antenne ochreous; thorax bright purplish pink ; abdomen fulvous yellow ; pectus and legs ochreous tinged with red-brown. Fore wing with narrow pure white costal fascia, the rest of wing bright purplish pink, suffused with red-brown to median nervure and veins 4. Hind wing ochreous white, the costa slightly tinged with brown. i Assam, Khasis, 1 ¢ type. Hap. 26 mm, (4) EMMALOCERA LONGIRAMELLA, Emmatocera longiramella Hmpsu. Rom. Mém. viii. p. 315, ols As i a) CEO (QUEENSLAND. (5) *EMMALOCERA RADIATELLA. Emmalocera radiatella Hmpsn, Rom. Mém. vin. p. 315, pl. 52. f. 21 (1901). (J)UEENSLAND. (6) TEMMALOCERA ACTINOLEUCA, Sp. Nn. 3. Head and thorax pale purplish pink mixed with white ; abdomen creamy white, dorsally fulvous yellow towards base ; antennz white; frons, palpi, pectus, and legs white suffused with rufous. Fore wing pale purplish. pink, the veins, two streaks in the cell and one in submedian fold white. Hind wing white faintly tinged with ochreous. SieRRA LEONE (Clements), 1 ¢ type. Hap. 24 mm, 128 SIR GEORGE HAMPSON ON THE (7) TEMMALOCERA DEPRESSELLA. Melissoblaptes depressella Swinh. P. Z. 8S. 1885, p. 876, pl. 57. f.5; Hmpsn. Moths Ind. iv. p. 63; id. Rom. Mém. vui. p. 324, ples Gadel. Polyocha saccharella Dudgeon, J. Bomb. Nat. Hist. Soc. xvi. p. 405 (1905). ApEn; PunsaB; Benegau; Bompay. The larva feed on the roots of sugar-cane. (8) TEMMALOCERA STRIGICOSTELLA. Polyocha strigicostella Hmpsn. P. Z. 8. 1896, p. 270; id. Rom. Mém. viii. p. 315, pl. 31. f. 18. ADEN. B. (Emmalocera). Antenne of male with short uniseriate branches. . (9) rTEMMALOCERA LEUCOCINCTA. Crambus leucocinctus Wik. xxvii. 169 (1863); Hmpsn. Rom. Mém. viii. p. 316, pl. 36. f. 9. Emmalocera crenatella Rag. Nouv. Gen, p. 38 (1888). SINGAPORE; BoRNEO ; PHILIPPINES. C. (Papua). Antenne of male laminate, serrate towards base. (10) PEMMALOCERA SANGUIFUSALIS, Polyocha sanguifusalis Hmpsn. P. Z. 8. 1910, p. 493, pl. xl. if O N. RHODESIA. (11) fFEMMALOCERA AURIFUSELLA. Crambus aurifusellus Wik. xxxv. 1756 (1866); Hmpsn. Moths Ind. iv. p. 62; id. Rom. Mém. viii. p. 317, pl. 36. f. 18. Kasumir; Punzap; Bompay; MApDRAs. (12) EmMMALOCERA BIFIDELLA. Polyocha bifidella Wileman, Trans. Ent. Soc. 1911, p. 357, pl. 31. f. 22. JAPAN. (13) TEMMALOCERA POLYCHROELLA, Sp. Nn. Head and thorax ochreous mixed with fiery red; abdomen ochreous ; antennz of male with the tuft blackish on inner side ; palpi, pectus, legs, and ventral surface of abdomen ochreous tinged with red-brown. Fore wing with narrow creamy white costal fascia leaving the costal edge red-brown towards base, defined below by a fiery rufous streak to beyond middle, the area below it red-brown to median neryure and vein 4; the inner PYRALID#, SUBFAMILY HYFSOTROPIN. 129 half of wing yellow thickly irrorated with fiery red, the terminal half of inner margin tinged with brown. W. Arrica (Dudgeon), 1 $,1 9; 8. Nigeria, Mama (Dudgeon), 1 $type. Hap., § 22, 9 28 mm. (14) EmMMALOCERA UMBRICOSTELLA. Emmalocera umbricostella Rag. Nouv. Gen. p, 38 (1888); id. Rom. Mém. viii. p. 316, pl. 36. f. 10; Hmpsn. Moths Ind. iv. p- 62. Corea; C. Caixa; Srkuim ; Borneo, Pulo Laut; PHILIPPINEs ; JAvA; FLores; Batt. (15) EMMALOCERA LUCIDICOSTELLA. Emmalocera lucidicostella Rag. Nouv. Gen. p. 38 (1888); id. Rom. Mém. viii. p. 316, pl. 35. f. 20; Hmpsn. Moths Ind. iv. p. 62. Punsas; Benegal; CEYLON; SUMATRA. (16) EMMALOCERA ANERASTICA. Nephopteryx anerastica Snell. Veth’s Midden-Sumatra, Lep. -p. 81 (1880); Rag. Rom. Mém. viii. p. 317, pl. 36. f. 8. SrerRA LrEonE; Formosa; PungaB; NicoBpars; JOHORE; SELANGOR ; SINGAPORE; SuMATRA; BorNEo, Pulo Laut; PHrtiip- PINES ; LovuisiIAvDE Is., St. Aignan I. (17) EmMMALOCERA LATILIMBELLA. Papua latilimbella Rag. Bull. Soc. Ent. Fr. 1889, p. cexx; id. Rom. Mém. viil. p. 313, pl. 36. f. 7. Polyocha rhabdota Turner, Pr. R. Soc. Queens]. xviil. p. 122 (1908). ' Polyocha achrosta Turner, Pr. R. Soc. Queensl. xviii. p. 122 (1903). N. GuINnEA; QUEENSLAND. D. Antenne of male laminate, not serrate towards base. (18) EmMALocERA LAMINELLA. Emmalocera laminella Hmpsn. Rom. Mém. viii. p. 318, pl. 51. f. 8 (1901). SrerrA LEONE; Br. E. Arrica; Br. C. AFrica. Sect. II. Palpi of male downcurved ; maxillary palpi filiform. A. Antenne of male with sinus and ridge of scales at base of shaft. a. Antenne of male with long uniseriate branches. (19) EMMALOCERA VARIEGATELLA. Polyocha variegatella Rag: Nouv. Gen. p. 39 (1888); id. Rom. Mem. viii. p. 326, pl. 36. f. 16; Hmpsn. Moths Ind. iv. p. 63. PUNJAB. Proc. Zoot, Soc.—1918, No. LX. 9 130 . SIR GEORGE HAMPSON ON THE (20) TEMMALOCERA TRICOLORALIS. Polyocha variegatella Hmpsn. J. Bomb. Nat. Soc. Hist. xii p. 320 (nee Rag.). Polyocha tricoloralis Hmpsn. J. Bomb. Nat. Hist. Soe. xv. p. 20 (1903). SIKKIM; PHILIPPINES. (21) EMMALOCERA DIVERSELLA. Polyocha diversella Hmpsn. J. Bomb. Nat. Hist. Soe. xii. p- 310 (1898); Rag. Rom. Mém. viii. p. 324, pl. vi. f. 21. Mapras, Nilgiris. (22) *EMMALOCERA COSTELLA. Polyocha costella Rag. Nov. Gen. p. 39 (1888); id. Rom. Mém. vill. p. 326, pl. 36. f. 15. GAMBIA. (23) EMMALOCERA CREMORICOSTA, Polyocha cremoricosta Rag. Bull. Soc. Ent. Fr. 1895, p. cii; id. Rom. Mém. vill. p. 325, pl. 51. f. 9; Staud. Cat. Lep. pal. ii. p. 13. Asta Minor; Syria. (24) TEMMALOCERA ERYTHRINELLA. Polyocha erythrinella Rag. Nouv. Gen. p. 38 (1888); id. Rom. Mem. viii. p. 323, pl. 44. f. 14. N. Nigeria; Apyssinta; Br. E. Arnica; Br. C. AFrica. (25) *EMMALOCERA CARNATELLA. Polyocha carnatella Rag. Nouv. Gen. p. 39 (1888); id. Rom. Mem. vii. p. 325, pl. 35. f. 25; Hmpsn. Moths: Ind. iv. p. 63. Pungas. » (26) *KMMALOCERA MONOCHROMELLA. Polyocha monochromella Rag. Nouv. Gen. p. 39 (1888); id. Rom. Mém. vui. p. 325, pl. 36. f. 13; Staud. Cat. Lep. pal. ii. Oo Las (27) rEMMALOCERA EREMOCHROA, sp. n. Q@. Head and thorax whitish suffused with ochreous brown; abdomen creamy white, dorsally fulvous yellow towards base ; pectus, legs, and ventral surface of abdomen white tinged with brown. Fore wing pale ochreous, the costal half and terminal area suffused with brown, the cell and veins beyond it with some whitish irroration, the interspaces beyond the cell with PYRALID®, SUBFAMILY HYPSOTROPINA. leat slight ochreous streaks, the area below the cell with slight red- brown irroration. Hind wing creamy white. W. AusrrawiA, Sherlock R. (Clements), 1Q type. Hap.44 mm. b. (Lodiana). Antenne of male serrate. (28) EMMALOCERA UMBRIVITTELLA. Lodiana umbrivittella Rag. Nouv. Gen. p. 38 (1888); id. Rom. Mém. viii. p. 319, pl..35. f. 19; Hmpsn. Moths Ind. iv. p. 62. Polyocha venosella Wileman, Trans. Ent. Soc, 1911, p. 357. JAPAN, Yezo; PuNJAB; SIKKIM; ASSAM. (29) EMMALOCERA ALBICOSTALIS. Lodiana albicosialis Hmpsn. Trans. Ent. Soc. 1900, p. 375; Staud. Cat. Lep. pal. ii. p. 13. PaLEsTINE; Punsas. B. Antenne of male without sinus and ridge of scales. (30) EMMALOCERA SUBFASCIATELLA. Polyocha subfasciatella Rag. Ann. Soc. Ent. Fr. 1887, p. 258 ; id. Rom. Mém. viii. p. 328, pl. 36. f. 17; Staud. Cat. Lep. pal. ii. p. 13. ARMENIA; PERSIA. Auctorum. Polyocha rhodesie Strand, Archiy. f. Naturg. 75. 1, 3, p. 384 CQO) ear Mey scnrscs-cs § earth race: Pe arheiabeen doslomtya N. Ruopesia. GENERA AUCTORUM. Barberia affinitella Dyar, Proc. Ent. Soc. Wash. vii. p. 39 (HGS), Tae VEMOMAV IAD ~ Sense de obacsapoocese noobs U.S.A., Texas. Cabmia myronella Dyar, J. N. Y. Ent. Soc. xii. p. 108 (1904), 1A har SKLO UO eate ROMER one oto aco coaNe rene U.S.A., Washington. Fondoukia translucidella Chretien, Bull. Soc. Ent. Fr. 1911, Pepe tan! DENI DEs cious erect etn cise sie oki. eae a Banos ALGERIA. Schenectadia merilesella Dyar, Pr. U.S. Nat. Mus. xlvii. p. 349) (1913) mr. Winerastia sc. Hes ccamenscces reels PANAMA. Sabormania pia Strand, Arch. Naturg. 78. A. Hft. 12, p. 80 OU. CMO OOO DQAND coo sbbiccoosscnoneone SPANISH GUINEA. ao patel . AEP ON VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 1338 6. First Report on the Inheritance of Visible and Invisible Characters in Silkworms. By Miss Maupz L. Ciec- HorN, F.Z.8S., F.L.S., F.E.S. [Received December 3, 1917: Read March 9, 1918.] The mulberry silkworm races of Bengal are all with the excep- tion of one (Bombya textor) multivoltine, but their cocoons are not so good as those of the European or Japanese races, and therefore when the question of reviving the Indian silk industry arose, the following suggestions were put forward, viz.: that endeavours should be made to obtain an improved multivoltine race by crossing an indigenous variety with a European one, and that our knowledge of hybridization according to Mendel’s law should be utilised to help in the process. With these suggestions in my mind I obtained from Italy, in December 1910, some European silkworm seed (eggs of the Bombyx mori) and some Nistri (Bombyx croesi) seed cocoons from the Berhampore Government Nursery. The European seed was of the Italian-Japanese Hybrid, and was the first generation of a cross between the univoltine (pro- ducing one brood a year) yellow Italian (Indigeno giallo) male, and the univoltine white Japanese female—pure yellow Italian seed not having been available at the time. This Italian-Japanese Hybrid is very hardy, being a first cross, and so I started my cross-breeding experiments with it. The cocoons of the multivoltine Nistri silkworm weighed (with the chrysalis removed) from 1 grain to 1°6 grains, whilst the cocoons of the Italian-Japanese Hybrid (being of a univoltine race and therefore bigger) weighed from about 2°5 grains to 4°6 grains. My aim in my experiments with these two varieties of silkworms has been (1) to make a multivoltine race (because though its cocoons are smaller than those of the univoltine, yet they are compensated for by the numerous broods produced during the year), producing cocoons of about 4 grains in weight, and (2) to see how far the good qualities of the univoltine varieties can be combined with the multivoltine character. I made two series of experiments :— A. Across between the multivoltine Nistri 2 and the univoltine Italian-Japanese Hybrid ¢. B. A cross between the univoltine Italian-Japanese Hybrid ? and multivoltine Nistri ¢. Experiment A was made with individuals selected usually from three or four families in each generation, except in one of the experiments in F,, which was made with a whole family. Experiment B was made with the complete family in each generation, with the exception of F,, when only a few worms were reared out of four layings. The layings produced in F, by Experiment A and those aaa 134 MISS MAUDE L. CLEGHORN ON THE INHERITANCE OF produced by Experiment B were entirely different from each other, for they resembled the maternal parent in each case, all the layings of the Nistri 9 and Ital.-Jap. ¢ being multivoltine, and all those of the Ital.-Jap. 9 and Nistri S$ proving univoltine. Result of the Hxperiment as regards the Size of the Cocoon. Experiment A.—The parent cocoons of the Ital.-Jap. 6 and Nistri 2 cross weighed 2°9 and 1:5 grains respectively. The cocoons of the first pencration of this cross resembled those of the Nistri (¢. e. the maternal parent) more than those of the Ital.- Jap. parent, being rounded at both ends and very thick but of the loose texture of the Nistri, the firm texture of the Ital.- Jap. being entirely unrepresented. They were uniform in size and shape, but varied in weight from 2°5 to 4:1 grains. In the second and the immediately succeeding generations, the cocoons were not so uniform in size and shape. Many were large and rather pointed at the ends, whilst they were all thinner and firmer than those of F,, and I found that in the earlier generations moths which gave complete multivoltine layings had nearly always cut out from cocoons which were about 3 grains or less in weight. I did not make use of these 3-grain cocoons for rearing purposes, even though they were far better than the original maultivoltine Nistri cocoon, but I carefully selected the best out of the most multivoltine layings of cocoons weighing from about 3°5 grains to 5 grains in weight. The cocoons in all the generations of the cross were far superior to the original Nistri cocoon, and in many of the generations they are also superior to that of the Ttal.-Jap. Hybrid. Up to F, many of the cocoons were 4 grains in weight, in F,, F,, F,, many were over 4:5 grains, while some weighed 5 grains and over. In F, and F, there were no 4-grain cocoons, and on the whole the cocoons of these two generations were very poor compared with those of the preceding generations, but they were nevertheless still superior to the original Nistri cocoon. As the layings from which these cocoons were produced were nearly entirely multivoltine, the cocoons appeared to be also becoming more multivoltine in character. The rearings in I, from which HF, hatched were all entirely multivoltine, while the F, silkworm were better again and seriposited cocoons, nearly all of which were over 3'5 grains, many over 4 grains, and some nearly 5 grains in weight (with chrysalis and outer fluff removed). The layings of the moths from these cocoons were also entirely multivoltine, which showed that it is possible to obtain a 4- or 5-grain cocoon from entirely multivoltine layings in F, after a cross without any recrossing. Care was, however, always taken to have the parent moths as distantly related as possible. (Table 1.) In this experiment I found that, after the direct influence of the fresh cross seemed to have disappeared, every third generation produced the best cocoons, for the cocoons of F,, F,, F,,, F,; VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 135 TABLE AK, SHOWING THE DESCENT OF COCOONS UP TO THE NINTH GENERATION, WITH DATES OF ELEV AGES. Ital.-Jap. Hyb. 3, Nistri? bere estet eh pate alsietr Jan. 31,1911 No. 1, 2°9 grs. No. Af? 1°5 grs. No. 229 ~No.15g No.269 .No.18¢ ............ March 28 _,, 37 grs. “38 grs. 338 grs. “28 ers. . | ; | No. 26g x IOs 8} soooagonsgomoosuce> ANE) BI} 5 4:2 gys. 3°7 grs. No.489 No.21¢ No. PAUSE sacndoseuesaodscal QUAY (Ol na 4-1 grs, 51 grs. “5 grs. No. 59 g No.152 No.6? No. 4g berenert July 8 ,, . , 3°8 grs. 4°3 grs. 48 grs. 5 grs. No. 52g No.19 No. 259 .No.183 No. 15? No.50g No.52g... Aug. 30 ,, 4 ors. a8ers. 44ers. “34ers. BG grs. “32ers. 4 ers. No.10g | No.5? No.1g No.179 VENCMIGE ee Oc oes 2°2 grs. ~ 28grs. 36 grs. 3'6 gers. 3'6 grs. No. 41 ¢ No. 55 ? No. 619 No. 27g NOSE E soocancnosea NOW BO gp, 2°5 grs. 2°4 ors, 19 grs. 2°9 grs. 2°5 grs. : No. 402 y No. 37 8 WOZBE! A NIOs, ZOO " .ccoossavavacsanvocndenssepecoonoceo» IHG, IL, TENA 3 ors. 28ers. 22ers. “24 ors, WUUH NGpInE) NU) WG PeM MeL OSes ye eee oes | RUCK oD ra 37 gers. 48ers. 41 grs. 4ers. 3°38 gers. ~ were much superior to those of the intervening generations. Even those of F,, seriposited during the rains in July were much better than those of F,, (April) and F,, seriposited in October. As the raiyats in India grow about three or four crops of cocoons a year (only rearing a few to keep the breed alive when they are short of leaf) it would be to their advantage to arrange that the crops reared are of every third generation. The cocoons obtained from this multivoltine race are much superior to the Nistri; those of F, were valued at about 94 francs per kilo in the Milan market, which is close up to the price of good Italian cocoons, and the cocoons of F,,, which were not near as good as those of F,, were valued at about 7 francs per kilo. The correct rendement could not be obtained, as the 175 cocoons sent to be tested were too few, 1 lb. weight. of cocoons being necessary. F4 Fs Fy A Ne Se ee ae ee ee ee ee a — a ee ee 136 MISS MAUDE L. CLEGHORN ON THE INHERITANCE OF Experiment B.—Cross between univoltine Ital.-Jap. Hybrid ¢ and multivoltine Nistri ¢. This was carried out for four generations only and then discontinued, as the cocoons were not as good as those of the reciprocal cross, rarely averaging a weight of 3°5 grains. Results of Experiment as regards the Multivoltine and Univoltine character of the Silkworm Moths. Experiment A. TABLE 2, ILLUSTRATING THE DESCENT OF THE UNIVOLTINE CHARACTER IN THE CROSS BETWEEN IrAu.-JAp. ¢ AND Nisrri 9. Multivoltine Nistri 9 Xx Univoltine Ital.-Jap. ¢......0......... Tnayines\allanultvooueiveu eee ee eee ee Many mores than és. 22 layings univoltine. 30 layings almost univoltine. 6 half multivoltine More gs than 9s. 6 layings univoltine. 16 about half univoltine. 2 multivoltine ............ More 9s than és. A few layings univoltine. One 75% multivoltine. Many partly multivoltine ... More gs than 9s. One 75 °/) multiyoltine. 2 half multivoltine. 15 partly multivoltine ds and 9s about equal. All Faboutehalifemnlliivoltin cies nese neem eee ee eee eee nari Nearly all about half multivoltine. A few about: 75/9 multivoltine............ Nearly all completely multivoltine All multivoltine All-multivoltine Vo eves ves oie. teas. ccahereene Jey Fy FP; Fy Fs Fy VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 137 From the results obtained it will be seen that all the eggs in the layings of the multivoltine Nistri 9 when crossed with the univoltine Ital.-Jap. ¢ hatched, 7.e., the layings were all multivoltine, whilst the univoltine paternal parent had no visible effect on the character of the layings. This showed that the multivoltine character was dominant in the 9, but recessive in the ¢. Toyama, the Japanese authority on silkworms, also found that in crossing pure breeds the first cross always. resembled the maternal parent. I usually found that the completely multivoltine layings did not give the most multivoltine results as might be expected, but the half multivoltine laying produced the least number of univoltine layings in the long run. In the Nistri @ and Ital.-Jap. ¢ cross I discarded. the multivoltine layings which appeared in the earlier generations, and mostly selected from the half, or partly multivoltine layings, till in F, when most of the layings were almost entirely multi- voltine. Some of the families have been entirely multivoltine since F., others have had a few partly univoltine layings, but in none of the generations since F, have any of the layings been - entirely univoltine. Toyama does not give any detailed account of the results he obtained in the brood characters. It would have been interesting and useful, as. the inheritance of these invisible characters appears to be complicated. He selected from multivoltine forms, but does not say if they were entirely ov partly multivoltine. He states as follows :—“ Those forms raised from the first cross do not remain true to the parents in subsequent generations. Even when we selected multivoltine forms for five generations we failed to get any constant multivoltine breed.” In his interesting pamphlet “ Sulla riproduzione degli Incroci’ Dott. Quajat, when referring to his experiments with bivoltine and univoltine races, states “that “nelle successive riproduzioni, bivoltinismo tende a ‘diminuire, ed alcune volte anzi a scomparire completamente. Sara oria interessante constatare se le ovature ottenute univoltine, abbiano allo stato lateute il bivoltinismo, e se questo si potra manifestare in seguito a nuovi incroci 0 spontaneamente.” I found that from F, the layings began to show a great tendency to become completely multivoltine, and in those of the F,, moths, from which F,, worms hatched, only one laying out of the whole generation was half univoltine, all the others were completely multivoltine. To account for the 22 layings in F, appearing univoltine, the univoltine character must have dominated in the maternal parents of these layings. When a female F, was crossed with a “‘ pure’ multivoltine Nistri ¢ only 3 eggs out of 250 hatched, and from the results obtained, in the reciprocal cross, it was found that if the maternal parent was a pure univoltine none of the eggs hatched for about a year, and if she was a pure multivoltine all 138 MISS MAUDE L. CLEGHORN ON THE INHERITANCE OF 2 the eggs were multivoltine. As this female of F, had hatched from a completely multivoltine laying, it might naturally be expected that, when the paternal parent was pure multivoltine all the eggs laid would be multivoltine, but as only a few eggs hatched it showed that the maternal parent was dominant in the univoltine character, and that the dominance of the univoltine character was rabeniied by the F & from the paternal parent in which it was not a dominant character. It is clear that the female influences the reappearance of the character in a dominant form, and shows that the descent is of a sex-limited inheritance. In my experiments I found that the univoltine or multivoltine character of the maternal parent showed itself in the layings and not that of the paternal, for the character of the paternal parent always appeared to be masked or suppressed. - Besides the difficulties a sex-limited inheritance presents the univoltine and multivoltine characters are not visible in the moths but only in their layings, for moths which outwardly resemble the univoltine parent may have a multivoltine laying and wice versa. When all the moths of a generation are bred inter se the character of only the maternal ‘parents can be determined by the eggs laid; but to prove that the males and females of each generation are either homozygous or heterozygous, dominant or recessive, they have each to be bred with pure univoltines and multivoltines. So to find out the exact composition of all the moths in each generation would require a multitude of experiments, and I could not spare many moths from F,, for I knew that in F, only a very small percentage of eggs would hatch. “The layings in F, which were laid by the F, moths give a clue to the character of some of the parent moths in F,. For the maternal parents of the six univoltine layings (Table 2) must have been dominant in the univoltine character, and those of the two multivoltine layings, in the multivoltine character, but the sixteen 50 per cent. univoltine layings point to the maternal parents being heterozygous. Heperiment B. rom the results obtained in the Ital.-Jap. @ and Nistri ¢ cross (Table 3) it will be seen that although all the lavyings in F, were univoltine, yet there were some multivoltine, ‘and partly multivoltine layings in F,, F, and F,; and, again, though the moths of F, were neared from one of the multivoltine layings of F,, yet 37 layings of the F, moths were univoltine. For ty-seven moths from an F, family of the Ital.- -Jap. 2 and Nistri ¢ cross were tested with. pure multivoltine Nistri moths - and the results obtained were as follows :— (1) Out of 21 layings of the F, @s and pure multivoltine Nistri gs 19 layings were entirely univoltine and 2 entirely multivoltine. VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 139 (2) Out of 26 layings of pure multivoltine Nistri @sand F, ds all the eggs hatched, thus all being multivoltine. These results give a clue to the gametic composition of the F, moths, for they shew (1) that 19 F, Qs were dominant in the univoltine character and 2 in the multivoltine character. (2) that all the F, gs which may have been univoltune were recessive in the univoltine character. 4 TABLE 3, ILLUSTRATING DESCENT OF THE UNIVOLTINE AND MULTIVOLTINE CHARACTER IN THE CROSS BETWEEN THE UNIVOLTINE ITAL.-JApP. 9 AND MULTIVOLTINE NistrI C. Univoltine Ital.-Jap. 2 X Multivoltine Nistri f..........0...0c00.8.. Py IDLER ANSE CHM), CCODUCTOG soovco sesq0psns ono posano obo oDaDs Mca osenne La ’ 11 2 moths 21 ¢ moths. 7 layings univoltine. 2 multivoltine. I halitimultivoltines wesseres ele ; ; 62 Ps. 84 gs. 37 layings univoltine. 2 almest univoltine. 2 multivoltine. 2 almost multivoltine. F3 34 9s. 47 gs. 14 layings univoltine. 7 almost univoltine. 4 almost multivoltine ......... Fy, (Discontinued) Unequal Sex-ratios. I had noticed that in the earlier generations of the Nistri 9 and Ital.-Jap. 3d cross (which were reared a year previous to that of the Ital.-Jap. Q and Nistri ¢ cross), the number of males and females seemed very unequal, and that in one generation males predominated, and in another, females. However, these remarkable fluctuations gradually decreased in the latter generations. _ In my second series of experiments, which were with the Ital.- Jap. 2 and Nistri ¢, 1 noted the exact number of males and females in each generation, and found that in this reciprocal cross the sex-ratios were also very unequal, but just the reverse in the character of the predominating sex, for in F, of the Nistri 2 cross there were many more females than males, while in F, of the Ital.-Jap. 2 cross there were more males than females. The unequal sex-ratios could be accounted for by supposing 140 MISS MAUDE L, CLEGHORN ON THE INHERITANCE OF that in some of the generations the univoltine females do not hatch, and in others the univoltine males, but in F, when all the eggs hatched the sex-ratios were also unequal. Method of Rearing of Worms. To ensure choosing distantly related moths for rearing from, IT reared the silkworms of each laying separately, and the cocoons were also kept separate by keeping the silkworms after their fourth moult in rounded trays with a double inner circle of plaited strips of bamboo, about an inch and a half from the outer edge, forming a space into which the silkworms readily crawl to sereposit their cocoons. When the cocoons are removed from the trays, they are placed in rows on large sheets of white paper on which is noted the number of the laying from which they were reared. Kach cocoon is covered over with a small earthen cup, the- common Indian chilum. A day or two before the moths come out, the cocoon is cut open to remove chrysalis and weighed. The weight is noted and the chrysalis put back. When the moths emerge, the pierced cocoons are removed from under the earthen covers and placed within the opening at the top of the covers for reference, and this also to prevent the moths from . getting out. By referring to the number of the layings and to the numbers of the two parent cocoons (which is also noted on the paper), the choosing of the distantly related moths for rearing is simplified. If I had been rearing on a large scale I should have kept four or six families separate for seven or eight generations, then bred them together, and from these again four or six families would have been separated out. In these experiments the silkworms have always been fed most during the night, as I have noticed that, in the wild state, the larvee of moths mostly feed up to 9 or 10 a.m., and then restart feeding at about 5 or 6 p.m. Even young silkworms, which I kept on a small potted mulberry plant under observation, hardly ate at all during the day, though surrounded by fresh leaf on all sides. I find that silkworms always eat most voraciously between 10 p.m. and 4 a.m., so it is unnatural for them to be forced to feed all day, which is usually the case by the native rearers, and may well be one of the causes of their degeneracy. They should have a rest of at least seven or eight hours during the day, and be fed every three or four hours during the night, starting late in the afternoon at about 6 p.m. If there is an abundant supply of leaf, they might with advantage be fed every two hours. Newly hatched worms should always be fed every two hours between 5 p.m. and 10 a.m. The worms if fed well in the last stage after the fourth moult will give good cocoons, even if not very well fed in the earlier stages, but it is most essential that they be well fed throughout the larval stage for them to be vigorous and healthy. VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 141 One of the advantages gained by the nocturnal feeding of worms is that the leaf can be gathered at sundown, and so keeps fresher, and does not fade as readily as when plucked in the morning. There is also very little chance of attacks from the dreaded silkworm fly, which is always on the alert during the brightest and hottest hours of the day. I have found that the leaf from male trees of Morus Indica gives better results in feeding silkworms than that of the female trees. The dicecious character of the mulberry is not, as far as I know, known to sericulturists, for in most handbooks on the subject they advise rearers to select trees which bear little or no fruit. The inconspicuousness of the catkins and pseudo-spikes of the mulberry has evidently led to the difference between the trees being overlooked by all but botanists. As the flowers are inconspicuous they are anemophilous, and the trees, when in flower in February, may be seen giving off pollen in little puffs like smoke. This is best observed when there is no breeze. Additional Observations made during Experiments. _ The inheritance of the visible colour character of the cocoons is clearly Mendelian. The parent cocoons of the Ital.-Jap. Hyb. were of the yellow Italian ¢ and white Japanese 9°. The colour of the yellow Italian cocoon is of a deep pinkish yellow (carneo-giallo or flesh colour), which sometimes varies from a deep orange to almost white, but never of the vivid yellow of the Indian cocoon. All the cocoons of F, of this hybrid were of a pale flesh colour, none were white like that of the Japanese parent. A character which dominates after a cross is made was described by Mendel as dominant, and, the character which seemed to have disappeared he called recessive. So the flesh colour of a cocoon is a dominant character, and the white a recessive. All observed results in the study of heredity point to the dominance of a character being due to the presence of that character, and the recessive to the absence of the dominant character. The flesh colour of the Italian is due to the presence of the flesh colour and to the absence of the vivid yellow colour of the Nistri. While the white colour of the Japanese cocoon is due to the absence of both the pinkish yellow and bright yellow colours —the example of the inheritance of eye-colour in man might make this clearer. Here the dominance of brown eyes can be traced to the presence of a brown pigment ; and the recessiveness of blue eyes to the absence of the brown pigment. All human eyes (except those of Albinos) have a layer of deep purple pigment on the inner surface of the iris, but in brown, hazel, green, and grey eyes there is also a layer of brown on the outer surface of the iris, and it is this brown layer which entirely (Gf abundant) or partly conceals the purple layer. In clear grey and clear deep and pale 142 MISS MAUDE L, CLEGHORN ON THE INHERITANCE OF blue eyes the brown pigment is absent and the purple pigment shows through the tissue forming the iris, and makes it appear of a clear deep blue, when the tissue through which it is seen is very delicate—and of a clear grey or pale blue when the tissues are more or less coarse. So, to trace the dominance of brown eyes the real nature of the various kinds of light eyes must be carefully made out; it then becomes clear that the presence of the brown pigment in brown eyes makes brown eyes dominant to blue eyes in which it is absent. If one parent has' very dark brown eyes and the other clear blue eyes, all the children will:have dark eyes, which sometimes include hazel, green or grey, but none will have clear grey or blue eyes. The reason for there being no blue-eyed children is apparent, for all the children inherit a factor, or unit character for pigment from the dark-eyed parent, but a factor lacking in pigment from the blue-eyed parent—and the presence of this pigment in all the children makes brown eyes dominant to blue. To return to the colour of the cocoons the simplest explanation will be found in the interaction of two simple Mendelian characters. These two characters are flesh colour-F, and yellow colour Y, and the two pairs of unit-characters involved are— 1. Flesh colour F. Absence of flesh colour f. 2. Yellow colour Y. Absence of yellow colour y. The parent moths, then, have the following constitution :— 1). Yellow Italian possessine the flesh colour and lacking the 12 Due 5 yellow colour of the Nistri Mee nae ae FF yy (2) Japanese white lacking both characters... oe ffyy (3) Nistri lacking the flesh colour and possessing the yellow colour ae bed ae key fey ed WAYSti The actual parents in the experiment were :— P, the Ital.-Jap. Hyb. an F, of a cross between the Yellow Italian and White Japanese. P the Nistri. 1 The Yellow Italian has a deep pinkish yellow (flesh coloured) cocoon, It inherits two factors, one for the flesh colour F, and one for the absence of the yellow colour y, from each parent, and so consists of the union of two similar pairs of factors Fy and Fy. The Yellow Italian is therefore pure (homozygous) as regards the colour, for the germ-cells (gametes) by the union of which it was formed, each carried the same kinds of factors Fy and Fy. So the gametic composition of the Yellow Italian for the colour of its cocoon is represented as FFyy in Table 4, Diagrams (1) and (2). As the whiteness of the Japanese cocoon is due to the absenee of both the flesh colour of the Italian, and the yellow of the 4 VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. 143 Nistri, the gametic composition is represented in small letters as ffyy (Table 4). There was no colour in either of its parents for it to inherit, for the gametes, from the union of which it was formed, bore the factors fy and fy. Table 4, Diagram (1). The cocoons of the Ital.-Jap. Hyb. are a pale flesh colour as they inherited the flesh colour from the Yellow Italian parent only, for the gamete from the White Japanese parent bore colour factors lacking in both the flesh and yellow colours. The colour factors inherited from the Yellow [Italian parent were By and from the white Japanese parent fy. The Ital.-Jap. Hyb. is . therefore not pure as regards the colour of its cocoon, for the two gametes, from the union of which it was formed, were unlike and did not carry pairs of similar factors. It is a hybrid (heterozygote), the gametic composition being Ffyy, and it will give gametes Fy and fy. When the Nistri (YYff), which has a deep yellow coloured cocoon, was crossed with the Ital.-Jap. Hyb. all the cocoons of I’, of this cross were of a bright yellow colour, but not quite the deep yellow of the Nistri. So the bright yellow of the Nistri was dominant to the pale flesh colour of the Ital.-Jap. Hyb., for the deeper yellow entirely masked the pale pinkish yellow of the flesh colour even when it was present (Table 4). The gametic composition of I’, of the Nistri 9 and Ital.-Jap. ¢ cross was YyFf and Yyff, and it therefore contained two classes, both numerically equally represented. ‘Table 4, Diagram (1).° All the cocoons were yellow, but not quite uniform in tin. The gametes given off by these two classes were :— YyFf giving YF, Yi, Fy, yf. VG oven een Gea au, In F, there were a few deep yellow cocoons like those of the Nistri, a good many bright yellow like those of F,, a few pinkish yellow and a very few white out of 52 cocoons. The exact numbers were—-13 deep yellow, 29 yellow, 6 flesh coloured, and 4 white out of 52 cocoons. The gametes for the colour character in I’, were YF, Yf, Fy, and yf, and their union at random would give, in F.,, cocoons of the following gametic compositions—YYFI, YYFf, Y Yff, Yyk ¥F, YyFf, Yyff, yy FF, yylf, and yyff, which resulted in cocoons of various shades with just a few white ones. This is just what occurred, and it will be seen that the proportions of the various colours obtained out of 52 cocoons run the proportion calculated very close, for according to the analysis in ‘Table 4 there should be 12 deep yellow, 24 yellow, 5 flesh coloured, and 7 white out of every 48 cocoons. ‘Table 4, Diagram (2). There was a difficulty, however, in distinguishing between the deep yellow and the bright yellow from the intermediate forms which occurred. In F, cocoons I found that in some cases when both the parent cocoons were deep yellow, all the cocoons produced by the offspring 144 MISS MAUDE L. CLEGHORN ON THE INHERITANCE OF were deep yellow too; in other cases, two deepish yellow F, cocoons produced some flesh-coloured and even white ones. T also found that flesh-coloured parent cocoons would, in some cases, give only flesh-coloured ones, and in others flesh-coloured and white. Table 2 shows that among all the yellows in F,, there are two kinds—the pure (homozygous) dominants Y Yff and YYFF and the hybrid (heterozygous) dominants Yyff, Yyl’F, and YyFf. So when YYff and YYff are chosen as the parents, all the offspring will produce deep yellow cocoons, but if YyFF and YyFf are chosen, about a quarter of the cocoons will be flesh-coloured, and if the light yellow Yyff and Yyff are chosen as the parents, about a quarter of the cocoons will be white. In his experiments with the white Japanese and yellow Siamese, Toyama obtained from the F, yellows some which produce ‘only yellows, and 2 yellow cocoons which gave 221 yellow and 77 pinkish yellow, and 2 yellows which produce 254 yellow and 77 white cocoons. These results obtained by him give almost the exact proportions (75 per cent. and 25 per cent.) I have obtained in my analysis of the colour factors, Diagrams (2) and (3) Table 4. Among the flesh-coloured cocoons they are two kinds—the homozygous FF yy and the heterozygous Ffyy. Parent cocoons. ‘which are both FFyy will produce all flesh-coloured ones, but two Ffyy parent cocoons will give a few white ones. Table 4, Diagram (3). Toyama appears to have obtained both the pure aml. impure flesh-coloured cocoons in his experiments. For, referring to them, he states “the pale-pinkish-yellow form pro- duces some uniform (produsine only pale-pinkish-yellow) and some mixed (the white 25 per cent. and the pale- pinkish- yellow 75 per cent.) offspring in each succeeding generation.” The pure white cocoon bred inter se always g gave white cocoons. The yellowish white cocoons. The yellowish- white ones, how- ever, mostly gave a small percentage of yellow cocoons. In the gametes of the pure white cocoons there is no colour factor, so when the parent cocoons are both pure white the offspring inherit only colourless factors and will all be white. Table 4, Diagram (3). The white recessives are also easily distinguished from the dominant yellows, and as they are pure (homozygous) in the colour character, a race with white cocoons can be easily made from white cocoons which appear in any of the generations. Toyama also found that “every white form from its first pro- duction remains true to itself.” The recessive character always breeds true in whatever genera- tion it occurs, but as it never is present in the I’, after a cross, the F, individuals must always be reared, as the recessives make their first appearance in F., On the whole the results of these experiments, excepting that 145 VISIBLE AND INVISIBLE CHARACTERS IN SILKWORMS. “SNYOd GIUAAH ANV AUNd AO YNIVdSAAO YNIMOHS “(¢) WVUDVIG (931 [TV) (ayy p “Ysop oped g “ysoy F) (‘moy]a4 TLV) Sfhh ffik ffhkk dCi g BME ler bie ilCrere Jeter Sree ee SLE K SILER BALA ARS SSA A SSA A “OUT M x “eq YM *paino[oo-Yysay x ‘Tgosinoyee- Ysoy “MOTTO x *MO[[oA snos{zoulofy SNOSAZOULOFT SNO3SAZ0.10}0 FT sno03{z0.10}0}] snos STRANDED ON THE BRITISH COASTS. 155 and its cranial characters agree with those regarded by True as belonging to adult females. The teeth are slender, with ‘a diameter of about 13 mm., and were completely concealed beneath the gun. Although the sex was not ascertained from observations made on the entire specimen, there can be little doubt that the animal was an adult female. The Cornish specimen was incomplete, the part recorded measuring 15 feet in length. Its teeth were uncut, and it was presumably a young male or female. The other specimen, 18 ft. 2 in. long, was definitely known to be of the male sex. Its teeth were large and massive, with a diameter of 35-37 mmm., and they projected beyond the gum. It thus appears probable that the teeth remain uncut in the female Cuvier’s Whale throughout life, unless they become external in old age, while in the male they are probably cut relatively early. The coloration of this species appears to be variable. Certain individuals have been recorded in which the upper part of the head was white; and the Wexford specimen possessed this type of coloration. In other cases the colour has been described as dark above and light below. (7) Sowersy’s WuAte (Jesoplodon bidens Sowb.). This rare species is represented by three records, from Inver- ness (Aug., 1915), Lincolnshire (Sept., 1916), and Wexford (Sept., 1914), respectively. The male Sowerby’s Whale is provided with a pair of large triangular teeth in the lower jaw, at about the middle of the length of the mouth, on either side. Females have a pair of similar teeth in the same position, but, so far as is known, always beneath the gum. The three specimens here recorded had their teeth concealed by the gum, and were presumably females. The Wexford individual was, however, definitely known to be of this sex. The Skegness specimen was reported to have been 18 feet in length, which is unusually long for this species; and it was white below—a type of coloration which has been reported by other observers, although Sowerby’s Whale is often completely black. A list containing 33 records of this species has been given by Kiikenthal (1914, pp. 98, 99). The Ziphioid Whales are said to feed principally on Cuttlefish ; and it is not impossible that the reduction of their teeth may be. associated with this diet. Piscivorous animals, such as the Delphinide and Crocodiles, seem to require a number of sharp teeth adapted for holding their prey. In the Ziphioids, teeth of this character are obviously not required ; and it may be suggested that the absence of teeth is an advantége to them, since the suckers of the Cuttlefish would probably attach themselves to such convenient pegs, were these present, and the operation of swallowing the prey might thus be rendered more difficult. It must not be forgotten, however, that the Sperm Whale, which is 156 DR. SIDNEY F. HARMER ON CETACEA also “‘teuthophagous,” has a specially strong series of teeth in its lower jaw. (8) KinLer or Grampus (Orcinus orca L.). A single record, May 1916, from the Solway Firth. The specimen, a male, was unfortunately incomplete, but the part remaining was 25 ft. 6 in. long; and the animal must have been at least 30 feet long when alive. ‘The species is very common on the Norwegian coast (Hjort, 1902, p. 120). It has been pointed out by Liitken (1887, p. 367) that a very remarkable alteration in the proportions of the fins takes place during growth in male Killers. While in young males, and in females throughout life, the fins are relatively small and weak, in the males all the fins —pectoral, dorsal and caudal—become disproportionately larger as the animal grows older. The difference between the small pectoral fins of the young male and those of the old male is described by this author as being ‘ per- fectly astonishing.” These alterations in the fins have more recently been described and figured by Grieg (1906, p. 9; see especially his figs. 2-6, showing alterations in form and size of the dorsal, caudal, and pectoral fins). The specimen from the Solway Firth was an excellent illus- tration of these statements. The dorsal fin was about 5 ft. 6 in. in height, while the pectoral limbs were 6 ft. 8 in. long and 3 ft. 7 in. broad ; thus greatly exceeding in absolute size those of a large Sperm Whale. While the pectoral limbs of young animals and of females generally measure about one ninth of the total length of the animal, those of the old males are as much as one fifth of the entire length. Assuming the correctness of this statement of Lutken’s, the total length of the old male here recorded would have been well over 31 ft. It seems probable that the female of this species hardly exceeds half the length of the largest males. The failure to recognize the occurrence of these changes in the males has resulted in the introduction of more than one specific name for the Killer. Grieg (1906) has given an account of a school of about 47 Killers which were observed on the Norwegian coast at the middle of January, 1904. Four of the females were ascertained to be pregnant, and others were accompanied by a calf. The young of 2°5 m. in length were regarded as not more than 2 months _ old; and those measuring 3°5 m. as being probably 1 year old. Birth and pairing are believed by Grieg to take place during the later months, of the year. O. orca may be easily recognized by its very large teeth, w hich have a basal diameter of as “arte as, 12 on-even 13,1n. and are 10 to 13 in number on each side of ene jaw, as well as by its strikingly marked black and white (or yellowish) coloration. A white patch behind the eye is characteristic, and the white area of the ventral surface, although variable in extent, typically STRANDED ON THE BRITISH COASTS. 157 sends up a lateral extension backwards on each side, behind the region of the dorsal fin. (9) BuackrisH ov Proor-Wuate (Globicephala melena Traill). Three records in the five years: Hampshire, 1913; Northum- berland, 1914; and Cork, 1915; all in March; besides a school of about 50 individuals which were stranded at Penzance on July 1, 1911. The Pilot-Whale reaches a length of at least 26 ft. and is usualy pert black. It possesses about 10 large teeth, about ji; in. in basal diameter, on each side, in the front half of each jaw. The ‘‘forehead” is enormously swollen, and the ectoral limbs are very long and narrow, reaching a length of about 4 ft.6in. It is well known to associate in large schools, which are hunted in the Orkneys, the Faroe Islands, and elsewhere. As many as 2000-3000 individuals have been driven ashore at one time on the coast of Norway (Hjert, 1902, p. 119); and a-record of 1000 specimens observed at the Lofoten Islands, on Sept. 4, 1890, has been given by Grieg (1897, p. 8). (10) Risso’s GRAmPUS (Grampus griseus Cuv.). Four records: Jersey, Aug , 1913; 8. Devon, Aug., 1917; and 8S. Devon, Nov., 1913; the last. record consisting of two individuals, presumably mother and calf, although the sexes were not definitely ascertained. It will be observed that all these records belong to the 8.W. extremity of the British Islands ; and there is little doubt that this is a more Southern species which only just reaches our seas. Risso’s Grampus i8 recognizable by its blunt head, without beak; and by the comer iille reduction of the number of its teeth. Of these, none are present in the upper jaw, while the lower jaw possesses 4 or 5, of considerable size, with a basal diameter of as much as ? ae at the front extremity. Adult individuals reach a length of about 12 ft. Flowers Memoir (1874) may be consulted for information regarding this species. (11) Borrie-Nnosep DoLrHin (Tursiops truncatus ee Ten records: one in February (Scilly Islands, 1915), one in May (Merioneth, 1916), and the remainder dma the period June-August. With the exception of one individual (Essex, 1914), the determination of which was not quite certain, all were from the Southern coast of England, or from the Welsh or Lancashire coast. The Bottle-nosed Dolphin reaches a length of about 12 ft., and possesses about 25 teeth on each side of each jaw. As in some other Dolphins, about two of these, at the front end of the series, are very small and usually remain concealed beneath the gum; while the remainder are relatively large, with a basal 158 DR. SIDNEY F. HARMER ON CETACEA diameter of as much as 7% in. As indicated by its name, the head has a well-marked beak, about 3 in. long. (12) Waire-BeakeD Doxpatn (Lagenorhynchus albirostris Gray). Eight records: one from the North coast of Ireland (March, 1917), one from the Island of Islay (Oct., 1913), and the remainder from the Eastern coast, from Caithness to Lincolnshire—to which may be added three specimens stranded in Suffolk and Kent in February, 1918. Although the two species are known to overlap in their distribution, it 1s noteworthy that in this series of observations the distribution of the White-beaked Dolphin and of the Bottle-nosed Dolphin have not overlapped and are complementary to one another. The White-beaked Dolphin is characterized, as indicated by its popular name, by possessing a well-marked short beak, which is white in colour. It reaches a length of rather more than 9 ft. Its teeth are about 25 on each side of each jaw, but are distinctly smaller than those of the Bottle-nosed Dolphin, their basal diameter being about ;4-73,; in. (13) Wurre-stpep DoipHr (Lagenorhynchus acutus Gray). Three records: I'air Island, between the Orkneys and the Shetlands (March, 1913); Lincolnshire (May, 1917); Co. Mayo (June, 1916). This species, which is said to be one of the commonest of the Cetacea off the Norwegian coast, where it may occur in schools of as many as 1000 individuals (cf. Hjort, 1902, p. 118), may be regarded as a boreal specres which does not often occur in our seas. Most of the specimens previously found have been from the Orkneys and other parts of Scotland; and one or two have been noticed from Ireland. So far as I am aware, the Lincoln- shire specimen here recorded is the first to have been obtained on the English coast. The White-sided Dolphin has a characteristic longitudinal whitish area on each side, in the middle and posterior half of its body. Its teeth are smaller (basal diameter about 5%, in.) and more numerous (about 30 to 35 visible during life on each side of each jaw) than in the White-beaked Dolphin, from which it differs in certain other respects, the following of which may be noticed. ‘The beak, which resembles that of ZL. albirostris, is black. ‘The pectoral fins are faleate, with a very convex lower border; those of the other species being blunter and broader, and less convex below. ‘These fins, moreover, originate from the white part of the body, being connected with the black part of the head by a narrow dark streak; while in ZL. albirostris the black of the dorsal surface extends as far as the base of the flipper (cf. Liitken, 1887, pp. 377, 386, 395). ZL. acutus is said to reach a length of about 12 feet (Hjort, 1902, p. 117). STRANDED ON THE BRITISH COASY'S. 159 (14) Common Dorin (Delphinus delphis L.). About 20 records, one or two of which have been not quite certain, though probable. Three individuals have been recorded from the Northern part of Ireland (Mayo, Donegal); two from the North-Eastern coast of Scotland (Inverness, Kincardine) ; one, somewhat doubtful, from Hast Angha (Suffolk); and the remainder, either from the English Channel, from Kent to the Scilly Islands, or from the entrance to St. George’s Channel, on both sides, from Cork (1918) to Wexford on the Irish side, and on the Welsh coast on the opposite side. None have been recorded in the North Sea area, from Forfar to Norfolk ; and none on the West coast of Scotland; which, however, has provided a curiously small number of records during the whole of these observations. The distribution thus indicated is in agreement with the supposition that this is an oceanic species which is frequently stranded on the more exposed parts of the coast-lines, but comparatively seldom makes its way into the North Sea. The three records from the S. coast of Ireland (including one for 1918) were obtained in February, that from Inverness in April, and the remainder from August to December. The Common Dolphin reaches a length of about 7 ft. 6 in. ; and is distinguishable by its very long beak and numerous conical uSen, of relatively small size, with a basal diameter of about sin. The teeth are more numerous than in any of the other species here considered, being about 45 in each half of each jaw. (15) Common Porpotse (Phocena phocena L..). Numerous records, indicating, as generally supposed, that this is the commonest species in British waters. Of those which were certainly determined, the great majority were recorded from the East coast of England, and most of them during the period May to August. Evidence has been obtained in support of the belief that the Common Porpoise gives birth to its young in the early summer, and that the length at birth is from 2 ft. to 2 ft. 6 in. According to Prof. Meek (1918, p. 197), the occurrence of Porpoises - near the coast during July and August may be regarded as an inshore migration for parturition and pairing. "This species differs from all others found on the British coasts in the form of its teeth, which instead of being conical, as in the majority of the species, are broadened at the Paes end ( ( spade- shaped”), although the exact form of the br pndlenedl part is variable. The teeth undergo a considerable amount of thickening as growth proceeds, and the broadened blade is not infr equently worn away in some of the teeth. About 25, or rather more, are present on each side of each jaw; though usually two, at the anterior end of the series, remain small omni are concealed below the gum. The length of the adult is about 5 ft. 6 in.—and this is distinctly the smallest of the British Cetacea. ‘The head is not provided with a beak. 160 DR. SIDNEY F. HARMER ON CETACEA MEMOIRS CITED, AxLEN, G. M., 1916.—“'The Whalebone Whales of New England.” Mem. Boston Soc. Nat. Hist. viii, No. 2, p. 105. Anpbrews, R. C., 1916.—‘* Monographs of the Pacific Cetacea,” IT. “The Sei Whale (Balenoptera borealis Lesson).” Mem. Amer. Mus. Nat. Hist. (n.s.) i. part vi. p. 289. Burrieib, 8. T., 1913.—*“ Belmullet Whaling Station.” Rep. 82nd Meeting (Dundee, 1912) Brit. Assoc. p. 145. Cocks, A. H., 1884.—“The Finwhale Fishery on the Coast of Finmark.” The Zoologist, (3) viii. p. 455. Cocks, A. H., 1887.—“'The Finwhale Fishery of 1886 on the Lapland Coast.” The Zoologist, (3) xi. p. 207. Cotterr, R., 1906.—“ Noele Meddelelsen om Naebhvalen (Hyperoodon), og Hvidfisken (Delphinapterus).” Bergens Mus. Aarbog, 1906, No. 6. Couxert, R., 1912.—** Norges Pattedyr.”” Kristiania, pp. 543-. Frower, [Sir] W. H., 1874.—“On Risso’s Dolphin, Grampus griseus (Cuv.).” ‘Trans. Zool. Soe. viii. p. 1. GrigG, J. A., 1897.—“ Nogle cetologiske notiser.” Bergens Mus. Aarbog, 1897, No. 6. Griea, J. A., 1906.—“Nogle notiser fra et spekhuggersteng ved Bildgstr@mmen i januar 1904.” Bergens Mus. Aarbog, 1906; Noy2: Haminron, J. K., 1915.—* Belmullet Whaling Station.” Rep. 84th Meeting (Australia, 1914) Brit. Assoc. p. 125. Haminton, J. E., 1916.—* Belmullet Whaling Station.” Rep. 85th Meeting (Manchester, 1915) Brit. Assoc. p. 124. Harmer, 8. }*.—‘“Report[s] on Cetacea stranded on the British Coasts during [1913-1917].” Published by the Trustees of the British Museum. 1914. No. 1, Cetacea stranded during 1913. MON TOs Des es Bs wo LOI, 1916 Not 3 ‘. 6 WSIS, TON Non et vy LONG: IIe, AO, fi, a eS Seige LS) Tse Harmer, 8. F., 1915.—‘*On Specimens of Cuvier’s Whale (Ziphius cavirostris) from the Ivish Coast.” Proce. Zool. Soc. 1915, p. 559. Hyort, J., 1902.—* Fiskeri og Hvalfangst i det Nordlige Norge.” Aarsberetn. vedk. Norges Fiskerier for 1902, i Hefte, Bergen (udgivet af Norges Fiskeristyrelse). KiKenruat, W., 1914 —“ Untersuchtmgen an Walen (Zweiter Teil),” VI., “Zur Kenntnis des Mesoplodon bidens (Sow.).” Jen. Zeitschr. li. p. 93. Tanur, 1D. G., 1910.—“ Observations on the Anatomy and General Biology of some Members of the Larger Cetacea.” Proce. Zool. Soc. 1910, p. 769. LirKken, C. *., 1887.—“ Kritiske Studier over nogle Tandhvaler af Slaegterne Tursiops, Orca og Lagenorhynchus.’ Vid. STRANDED ON THE BRITISH COASTS. 161 Selsk. Skr. (6), naturvid. og math. Afd., Bd. iv. No. 6 (Copenhagen), p. 337. Meek, A., 1918.—‘‘The Reproductive Organs of Cetacea.” Journ. . of Anat. li. p. 186. Mitiais, J. G., 1906.—“ The Mammals of Great Britain and Ireland,” vol. 111., London (Longmans, Green & Co.). MounsrernvetM, L., 1915.—“ Anteckningar om Hyperoodon rostratus ( Miill.) gjorda under en ishavsresa sommaren 1910.” Troms? Museums Aarshefter, xxxvii. 1914, p. 1. Murray, [Sir] J., and Huorr, J. 1912.—“ The Depths of the Ocean.”? London (Macmillan & Co.). Owen, [Sir] R., 1840-1845.—* Odontography.” Sars, G. O., 1881.—‘‘ Fortsatte Bidrag til Kundskaben om vore Bardehvaler.” Forh. Vid.-Selsk. Christiania, Aar 1880, No. 12. SourHwe 1, T., 1883.—‘‘On the Beaked or Bottle-nose Whale ( Hyperoodon rostratus). Trans. Norfolk and Norwich Nat. _ Soe. i. p. 476. Tuompson, D’A. W., 1912.—* Whales, Seals and Sea-Serpents,” in “Science of the Sea.” Edited for the Challenger Society by G. H. Fowler, ch. xii, pp. 383-402, London (John Murray). True, F. W., 1904.—‘ The Whalebone Whales of the Western North Atlantic compared with those occurring in European Water Ss, with some Observations on the Species of the North Pacitic.” Smithson. Contr. xxxiii. p. 1. True, F. W., 1910.—‘‘ An Account of the Beaked Whales of the Family ‘Ziphiide in the Collection of the United States National Museum, with Remarks on some Specimens in . other American Museums.” U.S. Nat. Mus., Bull. 73. TURNER, [Sir] W., 1871.—“* On the Capture of a “Sperm Whale on the Coast of Argyleshire, with a Notice of other Specimens caught on the Coast of Scotland.” Proc. Roy. Soc. Edinb. vil. p. 365. Turner, [Sir] W., 1872.—“ Adaonal Notes on the Occurrence of the Sperm- Whale in the Scottish Seas.” Proc. Roy. Soe. Edinb. vii. p. 632. Turner, [Sir] W., 1886.—On the Occurrence of the Bottle- Nosed or Beaked Whale (Hyperoodon rostratus) in the Scottish Seas, with Observations on its External Characters.” Proc. R. Phys. Soc. Edinb, ix. 1885-1888, p. 25. Turner, [Sir] W., 1904.—‘ The Occurrence of the Sperm Whale or Cachalot in the Shetland Seas.” Ann. Scott. Nat. Hist. 1904, p. 4. Turner, [Sir] W., 1912.—‘*The Marine Mammals in the Anatomical Museum of the University of Edinburgh.” London (Macmillan & Co.). Van Detnsz, A. B., 1918.—‘‘ Over de Potvisschen in Nederland gestrand tusschen de Jaren 1531-1788.” Zool. Meded. R. Mus. Nat. Hist. Leiden, Deel iv., Afi. 1, p. 22. 6 Proc. Zoou. Soc.—1918, No. XI. Wa kf pS Hie $e roomed ‘ON THE VARIATION OF THE PIT-VIPER 163 8. On the Variation of the Pit-Viper, Lachesis atrox. By Miss Joan B. Procrtsr, F.Z.S. [Received March 19, 1918: Read April 9, 1918.] (Text-figures 1-5.) INDEX. Page Variation and Aitiology (Evolution, heredity, etc.). Variation in Lachesis atrox ; derivation of markings.................. 167-180 Systematic (New names or changed names, or Varieties of L. atrox ; revisions, discussions, or elucidations affecting any part of the system, to be indexed under the names)... 163-167, 180 The distinction of the forms, whether they be regarded as species or as varieties, which cluster around the tropical American Pit-Viper, Lachesis atrowx L., and of which the principal are L. lanceolatus Lacepéde, L. jararaca Wied, and ZL. jararacussu _ Lacerda, is a subject which needs renewed investigation, especially in view of Dr. Vital Brazil’s recent publications*, in which he claims specific rank not only for L. lanceolatus but also for L. jararacussu, which hag generally been regarded as a mere colour variety. | Mr. G. A. Bouienger, who has kindly helped me with advice in my study of reptiles, suggested to me that I should take up this investigation, and he has given me not only access to the collection in the British Museum, of which he is in charge, but the benefit of his experience, especially as regards the bibliography of the subject. My best thanks are due to him for these favours. I, Hatsroricat.’ The number of names which Mr. Boulenger has quoted under the synonymies of LZ. atrow and L. lanceolatus is very great, but for my present purpose it will be sufficient to discuss only the principal, such as have had more general currency, or which are accompanied by figures enabling me to form an opinion on the forms for which they are intended. The earliest name is that of Coluber atrow Linneus, Mus. Ad. Frid. (1754) pl. xu. fig.2. The specimens are described as having— ventrals 200 and 196, subcaudals 70 and 67 pairs, and scales with “ carina elevate.” However, Mr. L.G. Andersson, Cat. Lin. type- spec. Sn. (Bih. Sv. Vet.-Ak. Handl. xxiv. iv. No. 6) p. 19, has been able to supplement this definition, as he has had access to the type-specimens in the Stockholm Museum, and he finds that the keels on the scales ‘“‘are low and extend nearly to the tip of the scales,” thus agreeing with Mr. Boulenger’s LZ. lanceolatus, * La Défense contre ’Ophidisme. S&o Paulo, 1911, 8vo. 2nd edition, 1914. dle 164 MISS JOAN B. PROCTER ON THE not with his Z. atrov. He counts 204 and 200 ventrals (v.), 67 and 70 subeaudals: (c.). Both descriptions appear to corre- spond with two specimens in the British Museum collection, from Martinique (Cat. Snakes, iil. p. 536, spec. 7 & s). Coluber lanceolatus Lacepéde, Hist. des Serp. (1789) p. 121, is based on specimens*in the Paris Museum: 228, 225 v., 61, 59 c. Habitat Martinique and perhaps Dominica and Cayenne. Figure worthless, probably from a bleached specimen. Dumeéril and Bibron (Erp. Gén. vii. 1854, p. 1505), under Bothrops lanceolatus, do not give us any particulars concerning the type-specimen, which- they must have examined, but the fact that the “« Vipére jaune de la Martinique,” also found in St. Lucia and Dominica, is the form intended. There can be no question as to the appli: cation of the name lanceolatus, the Fer-de-lance, which must be regarded as a strict synonym of L. atrox of Linnzeus according to Andersson. — - -Cophias jararaca Wied, Abbild. Nat. Bras. (1825), from BK. Brazil, 193-201 v., 59-68 c. The description and figure indicate a snake similar to Z. atrov, but with markings consisting of dark brown, darker-edged transverse bands, narrower on the back than on the sides, such as is figured by Jan, in Icon. Oph.: 47me livr. pl. 1ii., and corresponding to several examples in the British Museum collection from Rio Janeiro and Para (Cat. Sn. Ud. ps Dail, Spec. i, p. 539, spec. v). This variety must be the prevalent form in the Province of Bahia, as the following descriptions and figures of Wagler in Spix’s Serp. Bras. (hea) ave evidently veferable to it. Bothr ‘ops megera, p. OO, pl. xix. 195 v., 53 ¢c This figure shows dark olive upper parts with dark, darker-edged transverse bands and immaculate ventrals. B. furi ia, p. 52, pl. xx.: 201 v., 65 c. A uniformly coloured specimen nial may be ‘edkeorn to have lost its markings. B. leucostigma, p. 53, pl. xxi. fig. 1: ?v., 66c¢. Brownish, with darker transverse bands, ventrals powdered with grey. 3B. tessel- latus, p. 54, pl. xxi. fig. 2: 190 v.,%c. Dorsal markings as: in B. leucostiyma, ventrals checkered with brown. Bb. teniatus, p. 55, pl. xxi. fig. 8: Colours lighter than the above, transverse bands always double. Bothrops jararacussu Lacer da, Lee. sur le ven. des Serp.(1884) p.9. From the province of Rio de Janeiro. An adequate description of the striking markings of the Jararacussu is given (black above with yellow markings, Jongitulinal on the hea and obliquely pronged forks on the sides, yellow beneath spotted with black). Similar to the 5. atrox ficured in Jan, Icon. Oph. (47me livr. pl..u. fiy..3), and to two. specimens in the British Museum collection from Sao Paulo, presented by Dr. Brazil. Having thus indicated the sources to which I have referred in order to fix the exact meaning of the principal names which have had currency in the past, I w ill review the various opinions which have been expressed in the principal works on Ophidia. , VARIATION OF THE PIT-VIPER. 165 Schlegel (Phys. serp. (1837) pp. 532, 535, 537) recognises three species :—1l. TZrigonocephalus jararaca, from ,Sa0 Paulo, Sta. Catharina I., Sta. Cruz de la Sierra: 172-204 v., 44-62 c. From the description, this snake is the true Jararaca of Wied. 2. T. atrox: 190,196 v., 60, 68 c. Scales surmounted by a strong keel with tubercular tendency, in which respect it does not agree with the Linnean type specimen. Habitat N. Brazil, Dutch and French Guianas. 3. 7’. lanceolatus: 271, 220 v., 60, 60¢. Mar- tinique and St. Lucia. Scales surmounted by a simple keel. Colour of ventrals a clear greenish yellow. The description corresponds to the type-specimen of ZL. atrox as described by Andersson. Schlegel maintains that 7’. lanceolatus has a higher number of ventrals than the two preceding, but the number 271 is probably due to some mistake. Dumeril and Bibron (Erp. Gén. (1854) pp. 1505, 1507, 1509) describe three species :— Bothrops atrox, B. lanceolatus, B. jararaca. The only differentiation. made between the first two in the “Tableau Synoptique des Espéces du Genre Bothrops” (p. 1504), is that the ventrals of B. atrow are spotted, and those of B. lanceo- latws unicoloured. In describing B. atrox, however, they mention that the scales are more strongly keeled. B. jararaca is distin- guished from the preceding by a relatively obtuse canthus rostralis and larger scales on the snout. The description corresponds with that of the Jararaca of Wied. B. atrow. 29-32 scales. Habitat Dutch and French Guianas. B. lanceolatus. 271, 240, 220 v., 68, 64, 60 c¢.; from Marti- nique, Dominica, St. Lucia. B. jararaca. 172, 195, 204 v., 44, 62, 65 ¢.: from Sao Paulo, _ Sta. Catharina I., never in Surinam. The number of ventrals given by Duméril and Bibron do not seem very reliable, and 271 for B. lanceolatus is probably copied from Schlegel’s statement, which there is good reason to question. | Jan, Icon. Oph. 47me livr. Pl.i.: Bothrops lanceolatus (Merr.). Antilles? Geneva Museum. The specimen figured has 29 rows of scales. Markings irregular, but similar to those of two spe- cimens in the British Museum collection from Martinique (Cat. Sn. p. 536, spec. 7, s).—Pl.i.: 5B. atrow L., var. dirus Jan, from Buenos Ayres. Turin Museum. 25-27 rows of scales, with keels similar to those figured for 2. lanceolatus. The markings repre- sented in fig. 3 nnn. are matched by two specimens in the British Museum collection, from Sfo Paulo (presented by Dr. Brazil), and, as before mentioned, agreeing with those of the Jararacussu of Lacerda.—PIl. 11. fig. 4: var. tesselatus Neuw. Milan Museum. Another form of dorsal markings, similar to a specimen in the British Museum collection, from St. Lucia (Cat. Sn. p. 536, spec. v).—Pl. 11.: B. jararaca Neuw. Freyburg Museum. An excellent figure of the typical Jararaca; 25 rows of scales. 166 MISS JOAN B. PROCTER ON THE A. KE. Brown, in a paper in the Proc. Acad. Philad. 1893 (pp. 435-6), desexibes three species, but adds that he doubts their right to more than a varietal distinetion :—1l. Bothrops atrox, also aibed from two specimens from British Guiana; 196, 195 v., 42,99 ¢., 27, 27 rows of scales, which are broad, inte a high short keel not extending to the tip. Abdomen: unspotted. 2. B. lanceolatus, desoslyad from two specimens from Martinique ; 199, 200 v., 69, 69 c., 25, 25 sc. Scales longer than in B. atrox, and bearing a simple keel to the tip. 3. 6. jararaca, described from one specimen from, Brazil; 206 v., 57 ¢., 27 sc.; besides the annulated markings, Mr. Brown notes that the canthus rostralis is less sharp and the scales on the snout are larger than in the preceding species, a fact which was also obser raul by Dumeril and Bibron. G. A. Boulenger, Cat. Sn. vol. 111. 1896, pp. 535-537. Lachesis atrox. 161-216 v., 47-73 ec. L. lanceolatus. 180-240 v., 46-70 ec. Mr. Boulenger finds that the only distinctive character between these species is that of scale-structure. In the former the scales are “strongly keeled, the keels on the posterior part of the back very high, swollen in the middle, and much shorter than the scale.” In the latter the scales are merely “sharply keeled,” the keel extending nearly to their extremity. He also describes the ventrals of LZ. lanceolatus as yellowish, uniform, or powdered, or spotted with brown, and in this respect many of the specimens in the British Museum collection certainly disprove the state- ment made by other authors, that the ventrals of this snake are constantly immaculate. He adds that these species may have to be united, as some specimens of L. lanceolatus “approach L. atrox in the swelling of the scales at the base of the keels, and are thus intermediate between the two species.” Cophias jararaca and Bothrops jararacussu are placed in the synonymy of L. lanceo- latus. V. Brazil, Def. contre ’Ophidisme (2nd ed. 1914), pp. 78, 84, 88. L. lanceolatus. 195-200 v., 50-53 ¢. Tropical America. LL. atrow, 202 v., 55 ¢. Tropical America, less abundant than the above in the southern states of Brazil. L. jararacugu. 170-176 v. Brazil (Sao Paulo and Rio), In describing the first two species Dr. Brazil maintains that one of the main points of difference between these snakes lies in the ‘‘systeme de coloration” of L. atrox, of which he says: ‘‘ La coloration du fond, sur lequel se dessinent des figures pareilles a celles constatées dans l’espéce précédente (LZ. lanceolatus) est d’un gris rougeatre, parfois un ton gris cendré. Cette combinaison de couleurs donne un aspect velouté a Vanimal, ce qui permet de le reconnaitre a premiere vue.’ ‘The ground-coloun of L. lanceolatus is described as ‘“‘ vert tres foneé, gris et quelquefois Jaunatre,” and the abdomen ‘‘ vert foncé, parsemé de taches jaunes,” whilst VARIATION OF THE PIT-VIPER. 167 that of Z. atrow is of a “trés beau jaune clair marqueté sur les bords de noir ou de gris foncée”*. : In examining a large number of these snakes I have found the ground-colour to be equally variable in both; the ventrals may be yellow, yellow checkered with black, or of that greenish colour produced by a powdering of black over yellow, in either L. atrox or L. lanceolatus. It was therefore not quite clear to me why Dr. Brazil considers the general aspect and coloration such striking points, or how the latter should -produce a velvety appearance in L. atrox. Mr. Boulenger has looked into this. matter with me, using specimens of L. atrov and L. lanceolatus named and sent to him by Dr. Brazil himself. There certainly is a difference in the appearance of these specimens, but this is not due in any way to the markings, which are strikingly similar. The specimen marked “ atrow” has, however, the very prominently keeled scales mentioned before, and Mr. Boulenger has pointed out to me that the “velvety” appearance of this snake is entirely due to the consequently greater breaking up of light upon its dorsal surface, Dr. Brazil’s Z. atrox is therefore the same as Mr. Boulenger’s. L. jararacussu.—Dr. Brazil maintains the specific rank assigned to the Jararacussu by Lacerda: first, on account of its striking black and yellow markings; secondly, because of the comparatively low number of its ventrals; and, thirdly, because of its much more triangular head. With regard to the first point, there are specimens in the British Museum collection which can be graded to form a transition series from the typical L. atrox to the Jararacussu, a specimen from W. Ecuador being exactly inter- mediate between the two types of markings. With regard to the second point, the ventrals of the Jararacussu are as a rule fewer than those of Z. atrox. Dr. Brazil mentions 170-176, but two specimens received from him have 180 and 184, 180-240 ventrals is, however, the range given for L. lanceolatus in Mr. Boulenger’s Catalogue of Snakes, and, as I have failed to detect any structural differences in the shape of the head or in the scaling, I think that the Jararacussu cannot be regarded as more than a colour variety of L. atrow L. ’ TI, Form Aanp LEPIDOSIS. As I think I have shown in the annexed table that there is no correspondence between variations in markings and the number of ventrals and caudals, I will describe the differences in form and lepidosis which have led to the distinction of species. The most important is that of the two types of scaling found in L. atrox. It has been generally accepted that the high short * The coloured plates which accompany Dr. V. Brazil’s descriptions do not convey these supposed differences, and it is well to point out that but little care has been bestowed on the rendering of the markings. I think a L. lanceolatus with only about 10 markings on the body, as figured, to be an impossibility. 168 MISS JOAN B. PROCTER ON THE keel is proper to Z. atrov and the low long keel to LZ. lanceolatus. Dr. Andersson has shown, however, that the latter form is really the Coluber atrow of Linneeus. so that if the former is maintained as a distinct species on account of its scale-structure, it will be necessary to alter the name which has usually been given to it. I suggest that of ZL. affinis Gray, as the specimens of Bothrops affinis (Catalogue of Suakes (1849), p. 7, specimens J & 0), which I have examined, answer the definition, and this appears to be the earliest name which can be applied to it. The dorsal scale of the typical Z. atrox L. is of a long narrow diamond shape, usually about twice as long as broad, and bearing a simple keel extending to the apical pits. in the tip of the scale. That of ZL. affinis is broader in proportion, more rounded, and sometimes truncate behind ; it bears a short keel, supported upon an extremely convex area, leaving only a narrow margin of flat scale. This convexity of the scales is so pronounced in some speci- mens that they can be distinguished from the preceding form by touch alone. The scales of Bones specimens, however, are inter- mediate in type; they may be of the narrow form with the long keel distinctly swollen at the base, or, while maintaining the long keel of atrox, they may be both broad and convex as in affinis. Other individuals present scales of both the extreme types. On examining the middle third of the body in one of these, I find that the median dorsal scales are of the high short type, and the lateral dorsals of the long low type. Further examination shows that, in every case, the anterior part of the snake is of the atrox type and the posterior of the affinis type. The evolution of the scale-structure is thus clearly shown. The long low-keeled scale gradually broadens, whilst its keel swells along its base and shortens, until it becomes completely transformed into the affinis type. This transformation is, as described above, completed upon the median dorsal scales sooner than upon the laterals. As regards the snout of L. jararaca, its shape is very slightly different from that of Z. atrow, in that the canthus rostralis is somewhat more obtuse, and the scales of the upper surface are slightly larger than those on the vertex. These characters are not very distinct, as several specimens of the typical L. atrox present snouts of a similar form; in fact, one specimen (Cat. Sn. 11. p. 536, spec. v) is indistinguishable from L. jararaca (spec. g, Cat. Col. Sn. [1858] p. 226) in this respect. Duméril & Bibron, and A. E. Brown, both mention this point as one of the distinguishing features between the two forms; and Schlegel (Phys. Serp.), in his figure (pl. xix. fig. 1) of the dorsal view of the head of the Jararaca, represents the difference between the scales on the snout and those on the rest of the head as very considerable. This is certainly a peint of variation which I cannot consider proper to the Jararaca alone, having found no fewer than six young specimens of L. atrox with this characteristic. The different types of form and lepidosis described above are ' VARIATION OF THE PIT-VIPER. 169 therefore so inconstant, and so completely connected by inter- mediate forms, that they cannot in themselves be considered sufficient for the distinction of species. IIL. Sysrem or MArkines. Before discussing the evolution of markings and their individual variation, I will outline the general system of arrangement of markings common to all colour varieties of ZL. atrox. Asa working hypothesis on this subject, Mr. Boulenger drew my attention to Dr. Zenneck’s paper ‘t Die Zeichnung der Boiden ”*, and I have found that his theory—that the dorsal and lateral markings of Boids are made up of four paired longitudinal series t—is equally applicable in the case of L. atrox. Of these, only three are usually present, but in some specimens the fourth is present upon the head. It is the constant relationship between the spots of the series of one side of the snake which forms the regular pattern, but those of one side are quite independent of those on the other, thus accounting for the asymmetrical appearance of the markings on the median dorsal line, which is sometimes very marked ¢. When present on the head, the first or dorsal series commences as a streak, or a few broken spots. Occasionally it forms a. A-shaped marking with its fellow. On the body this series is usually the broadest and most marked, and, in individuals where it tends to disappear, it is always the last to go. The dorso-lateral or second series, when present on the head, may either consist of an oblique narrow streak or of broken spots of this streak, originating above the ocular shield, or of a cross-bar or blotch in front of the eyes. This second series is rather unstable on the body, for though it may be of equal development to the dorsal, it is more often hardly discernible and certain spots frequently become confluent with their neighbours of the first series. In some forms the markings of these two paired series form a single dark triangular area on the head, but are more often irregular and indistinct. The lateral series is always present on the head of those snakes exhibiting dorsal markings. It forms a broad black streak from the posterior border of the eye to the commissure of the jaws, usually passing through the sixth and seventh labials. Rays proceeding from it may be present on the other upper labials, or _may take the form of isolated spots. The post-ocular streak is always separated from the superciliary streak by a narrow area of the lighter ground-colour, and is sometimes also outlined in * Tiibing en Zool. Arb. iii. (1898). + These four series are termed Dorsal (D.), Dorso-lateral (D.L.), Lateral (L.), and Ventro-lateral (V.L.) by Mr. Boulenger, ‘Snakes of Europe’ (1913), p. 30. ~ This lettering is followed in my text-fig. 1. t+ Mr. Boulenger has drawn attention to this bi-lateral asymmetry in his op. cit. p. 33, and he mentions a specimen of Lachesis alternatus with 24 markings on the left side and 27 on the right. 170 MISS JOAN B. PROCTER ON THE cream-colour, which brings it out very sharply. On the body this series is well defined. The fourth or latero-ventral series is never presentjon the body, and not always upon the head. It is evidently a most primitive character, which has disappeared in many specimens. In the Text-figure Il most marked form this series only consists of three or four black spots on the lower labials, and one larger spot which has become confluent with the post-ocular streak. This latter spot is the last of the series to disappear, and is entirely the cause of the apparent broadening and lengthening of the post-ocular streak in VARIATION OF THE PIT-VIPER. 171 many snakes. This series must not be confounded with the outer ventral series, which commences on the chin-shields and is usually distinetly marked throughout the body. The markings develop upon regular lines, and the degree of this development varies on different regions of the body. That on the anterior end of the body is the most primitive, as I shall endeavour to show later on, but markings immediately behind the head are always irregular. In Lachesis atrox the spots of the series on each side of the body form themselves into distinct alternating groups, which I shall call A and B. Group B is less stable than A, and frequently disappears altogether, either temporarily in the evolution of the markings or permanently. Text-figure 2. Group A. Group B. On one snake the relative development of groups A and B is not always constant, but it is always alike on both sides of the body. Since group A is usually the best developed, it is this group which I have counted in giving the numbers of markings in the table of statistics. This number is not the same for the two sides of many snakes—another reason for the faulted appearance in the general dorsal pattern. The dorsal markings of Z. atrow are therefore made up on each side of three longitudinal series of spots, which in turn form themselves into alternating groups A and B. Each of these consists of six primitive spots, which, according to their presence, absence, or confluence, determine the variety of marking pro- duced. In order to follow their evolution and variation, T have numbered those of each group in order of their stability (see text-fig. 2), so that each may be referred to by a definite formula. The ground-colour appears to be formed by the varying pro- portions of a black (or dark brown) and a yellow pigment, the black being the more superficial. When the shade is greyish, there is a smaller proportion of yellow pigment. ‘The usual brown tints are composed of a very fine powdering of the dark pigment over the yellow. Quite apart from the regular markings, the scales 172 MISS JOAN B. PROCTER ON THE often each show a delicate arrangement of black pigment standing out from the ground-colour and having the same pattern effect as the fine dendritic marks seen in many rocks. This arrange- ment is often exactly repeated from one scale to another. When this style of markings is present on the clear yellow of the ventral shields, it produces a dark green effect, merging, when seen at a distance, into the ground-colour. IV. Inprvipuau VARIATION AND Eyouurion or MARKINGS. Individual Variation. As a starting-point in the study of the markings and colour varieties of ZL. atrox, it was suggested to me by Mr. Boulenger that I should make an examination of a female and her 26 young from Trinidad (received from Mr. Urich) in order to ascertain the amount of individual variation among specimens unquestion- ably pertaining to one form only. The young snakes range from 160 to 300 mm. in length, and are more brightly marked than their mother. Their ground- colour is a soft shade of brown, except the tip of the tail, which is a pale yellowish. Particulars as to the number of ventrals and subeaudalssetc. will be found in the annexed table. In the majority of cases, the pattern on each side is made up in the _ following way, as shown on text-fig. 3 :— Group A consists of the six primitive spots arranged in a pyramid (see text-fig. 2, p.171). A large triangular or rather trapezoid spot (A 1, dorsal series) forms the apex, and rests upon two small rhombic spots (A 5, 6, dorso-lateral series), which are sometimes confluent with it. These rest upon three similar spots, the outer ones being somewhat the larger (A 2, 4, 3, lateral series), This triangular marking is margined in cream-colour, and encloses an-area darker than the surrounding ground-colour, a state of things which seems to suggest a centripetal aggregation of pigment. Group A, though equal in size to group B, is in every case darker and more marked. Group B is also triangular in form, but the base coincides with the mid-dorsal line, instead of the apex as in group A. The said base is composed of three oval spots (B 5, 1, 6, dorsal series), the middle one being much the largest. Three more small oval spots enter the remainder of this triangle, the largest at the apex (B 3, 4, dorso-lateral, B 2, lateral). (Text-fig. 3, a.) When the markings of the two sides of the snake correspond exactly, the general dorsal design is a single string of light- spotted ovals on a dark ground; this is formed by the paired groups B having their bases applied together. They appear oval rather than diamond-shape, on account of the curved border of the ground-colour of these groups. If the markings should alter- nate with each other, a light wavy band on a dark ground is the general result. Usually, however, a single specimen exhibits VARIATION OF THE PIT-VIPER. 173! many different combinations of these forms, owing to the different: number of markings on the two sides. In most specimens mark- ings of one or more series are present on the head, and in several the latero-ventral series is very marked. Text-figure 3. Many specimens do not possess all the primitive spots described, especially upon the posterior part of the body, where the pattern becomes modified. In the first stage of this modification A 95 and 6 become confluent with A 1, which tends to divide into two triangular spots; the spots of group B, with the exception of Bland 2, merge into the background (text-fig. 3, c). Some specimens are of the more primitive type anteriorly only, whilst others have the markings of the greater part of the body of the slightly modified type, and become still further altered -on. their’ 174 MISS JOAN B. PROCTER ON THE posterior parts. One specimen, however (see Table, Trinidad 1 h), is inclined towards the Jararaca type of marking. Anteriorly A 1 is divided, each spot being confluent with A 5 and 6; A 4 is absent, and of group B only an occasional. B 1 is present (text- fig. 3,D). At about the middle of the snake the twin spots A 1, 1, have become some distance apart, and are in sufficiently close proximity to A 2 and 3 to give the appearance at a distance of paired transverse bands, or, since the intermediate space is darker than the surrounding ground-colour, of a single dark- edged band; these bands, which may pair with those of the opposite side or not, are very little more than their own width apart. In all specimens the pattern tends to break up into a spotted type just before the tail, all the spots being more or less equal in size and distribution. It consists of Al, 1, 4, 2, 3, and B 1, 3, 4, and 2. In the markings of the mother, A 1, 2, 5, 5, and 6 are con- fluent, forming a somewhat truncate chevron, in the middle of which A 4 is sometimes situated. Group B is made up of the six primitive spots, all except B 1, 2, however, being indistinct (text-fig. 3, B). On the whole, the individual variation shown by these 27 specimens is very slight ; the most apparent differences between them are due not to variation of thé actual markings, but to the inconstant relationship of those of the two sides of the snake. 1 have since examined another mother and young, from Anda- goya, Colombia (received from Dr. Spurrell), and in this case there is no variation at all among the young. The markings of both families are of the most primitive type oceurring in L, atrox, ail other forms being evolved from it, as will be shown presently. Evolution. In the course of evolution, these primitive markings become modified in the following way, which is the same for all forms of L. atrox. A 1 tends to divide transversely to the axis of the body, and A5and 6 become confluent with it. B5 and 6 merge into the ground-colour, A 4 and B3 and 4 disappear (this stage has already been described in the variations of the young snakes), A 1 then divides completely, but is still distinct from A 2 and 3,_ A 4 disappears, and the whole of group B tends to merge into the background. The spots A1, 1 then become a considerable _ distance apart, narrow, and in- close proximity with A 2 and 3, which, since the interspace is darker than in group B, thus produce the effect of a dark, darker-bordered, transverse band. Except for an occasional B1, this group is pale and quite indistinct. At this point the bands, which may or may not pair with those of the opposite side, are slightly more than their own VARIATION OF THE PIT-VIPER. 175 width apart. A 1,1 and A 2, 3 now become confluent, forming the dark unbroken marginal lines of the transverse band which constitutes group A: (text-fig. 4, A). These lines may be nearer together on the back than on the sides, and are sometimes much serrated. The bands, 7. e. groups A, gradually become further apart from each other, with the result that the markings are slightly fewer in number than in the primitive type. For the present I shall call this annulated form of marking Type II. It constitutes a distinct branch in the direct evolution of markings (text-fig. 3, a), Type III. evolves directly from the primitive Text-figure 4, arrangement, in exactly the same way as Type II. up to the point where A 1 is completely divided, but distinct from A 2 and 3. Al, 1 are, however, squarish, and form a square group with A 2 and 3, which they equal in size. In the course of evolution A 4, B 2, 3, and 4 reappear (text-fig. 4, B), and are also all of equal size. In this type A 4 belongs to the dorso-lateral series, being situated immediately above its position in the lateral series in Type I. In the evolution from Type I. to Type III. the series equalise, the dorsal narrowing and the dorso-lateral broadening. The general pattern is formed, therefore, of three series of equal . 176 MISS JOAN B,. PROCTER ON THE and alternating spots (text-fig. 4, c). Group A can only be distinguished from B by the fact that these spots are more square than those of the latter. In this type the ground-colour is not usually darker at A, as is the case in the preceding types. Text-figure 5. Further development of this type is shown on.a specimen from St. Lucia (Cat. p. 536, spec. v). On this snake both the dorso- lateral and lateral series are absent, or but faintly marked, the markings thus consisting of two squarish spots—A 1, 1— followed by one roundish spot—B 1—all of which are for the most part confluent with those of the opposite side. VARIATION OF THE PIT-VIPER. 177 The fourth type—Z. jararacussu (text-fig. 5)—constitutes the third branch in the evolution of the markings. A 1,5, 2,6,and 3 become confluent, forming a subcrescentic marking, in the middle of which A 4 may be present or not. All the primitive spots of group B unite together to form a dark triangular area, which in the course of evolution becomes confluent with group A—i. e., the apex of A with the base of B—along the dorsal line. At this point the markings darken, and the usual brownish, greyish, or olive ground-colour becomes a bright clear yellow. Finally, more and more black pigment becomes deposited at A and B, until the markings have usurped the place of the ground-colour, even the crescentic marking (A) being partially filled in with black. The general effect of 'l'ype IV. is therefore a black snake, with yellow forked markings issuing transversely from the yellow ventrals, which are checkered with black. The dorsal surface of the head is completely black, owing to the development and confluence between the streaks of the dorsal and dorso-lateral series. The post-ocular streak is separated from this area by a narrow stripe of the clear yellow ground-colour, which continues slightly below the commissure of the jaws. : The most striking feature about this type of marking is the clear yellow of the interspaces in the dorsal pattern; in other types this is only found on the ventral surface of the snake, the dorsal ground-colour always exhibiting a superficial powdering of dark pigment. It therefore seems probable that in the course of evolution this pigment has all aggregated in the spots of Groups A and B, and, as more and more becomes deposited, these areas further encroached upon the yellow ground-colour. V. PHYLOGENETIC RELATIONS BETWEEN THE TYPES. In tracing the evolution of markings from one type to another, I have assumed that the anterior parts represent the primitive pattern, as in lizards and many mammals (ex. Lacerta muralis, Equus quagga). It might appear, however, that in Z. atrox this is not the case, the more regularly spotted type, characteristic of the West Indies representing the original pattern, from which the clustered, annulated, and forked markings of C. and 8. American » forms were derived. On careful consideration I cannot adopt this view for the following reasons :—1l. The manner in which the pattern of the Jararacussu develops from Type I. into the complicated design of Type IV., and develops on each individual posteriorly until the tailis a uniform black, cannot be looked upon as primitive, and if this elaborate pattern, become simplified, is a further development of the clustered type of marking, the other forms must also be more advanced. 2. I hold the greater number of spots to be the more primitive (and for this assumption there is much correlative evidence among other snakes and lizards). 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Je je je T “901q.19g] - OD) BAIL ye Jee qourqsrpuy *BloLZ9U9 A ainosqo zB 09 Z6L Bay je Hig 4yen20e : PpeyIpoy BION “IG| Be 761 a GD ROE we aE We [eet fro santas TBSIOG SG 86 iad 66 19 916 je ul ur T vonbiuyieyy | 73 UG 8 9 861 ye 18 4B ‘adnojapensy IZ ra 0g 29 RBG je wv 1 [jerecce elo(nlelele}eiu syoiele nisi een ec cen peeve eee sscese qOULSIPUT : “padh2 BU10,A z (14 91 FL | PZ £9 681 je ye ye Leer tlees eee ccesce starve sence nescns pordhy on LT ‘901q.1eg SI Ait =| Se €9 981 je je je pur ‘vovininl ‘sunffy “WBA UaeMjoq o}eIpau1ezUy yzeig | 91 9 e 46009Stts«LGT. qe ye ye IROOM A CMENSS codsocachsoosodoonosoogseucnosase Prof. H. M. Lerroy, F.Z.S., Hon. Curator of Insects. Exhibition of a series of lantern-slides from photo- graphs taken in the Zoological Gardens, Sydney, ING Sp Wralest eo es cas tevaiasise a tamesdeauseaneacen conan The Secrerary. Report on the Additions to the Society’s Menagerie during the month of October, 1918......... Miss K. Lanner, F.Z.S. Description and exhibition of the method of preparing skeletons by the use of trypsin... Mr. KE. Hatscuex. Description and exhibition of investi- gations into the forms assumed by drops and vortices of gelatinan, various coapulamts) ka. -cy.sececeessn oe Prof. F. Woov-Jonzs, F.Z.8. Exhibition of a cast and set of Rontgen-ray photographs taken from a Chimpanzee which had died from pulmonary tuberculosis ......... PAPERS. 10. Comparison between the Lower Jaws of the Cynodont Reptiles Gomphognathus and Cynognathus. By Dr. Branistav Perrontevics. (‘Text-figures 1-8.)......... 11. On a new Genus of Extinct Muscardine Rodent from the Balearic Islands. By Dosoruza M. A. Bare, Hon. M.B.O.U. (Plate I. and Text-figures 1 & 2.)... 12. A Case of Hermaphroditism in a Lizard, Lacerta viridis. By Nort TaytEr, B.Sc. (Lond.). (From the Zoological Department, University of London, University College.) (Text-figures 1-3.) e@ececcosetrcecee Page 308 308 308 309 309 310 310 310 197 209 Vv Page 13. On two new Elasmobranch Fishes (Crossorhinus juras- sicus, sp. nov., and Protospinax annectaws, gen. et sp. nov.) from the Upper Jurassic Lithographic Stone of Bavaria. By Arruur S.1ra Woopwarp, LL.D., ESV Zi Sie i (blabe Ws) aiense toe cece als Seltcwie ects 231 14. The Function of Pathological States in Evolution. By WWloveroimie ISOS Sechonsned bang bostoodonepe none soSopHodGosOC 237 15. Notes on the Beavers at Leonardslee, 1916-1918. By Sir EpmMunp G, Loprr, Bart., Vice-President Z.S. ... 255 16. On the Madagascar Frogs of the Genus Mantidactylus Blgr. By G. A. Boutenesr, F.R.S., F.Z.8. ......... 257 17. Ciliary Action in the Internal Cavities of the Ctenophore Plewrobrachia pileus Fabr. By JAmEs FE. Gemmitt, M.A., M.D., D.Sec., F.Z.8. (Text- figumes MG e oii arse tera te Hicotrias alt wis.stuac eile) coe casera 263 18. On Seymouria, the most primitive known reptile. By D. M. 8. Watson, M.Sec., Capt. R.A.F., Lecturer in Vertebrate Paleontology, University College, ond ones (Rext— heures ll O)) nen ansctcne ie cmie ee err 267 Alphabetical MliistroteContriloutiors.....-sce se eceeee ests nee vii TIsaVG Kp Ge sees OR oe cD bs SNR DREN RMR nn nen Xl Lbs OL ; 4 1 ALPHABETICAL LIST OF THK CONTRIBUTORS, With References to the several Articles contributed by each. (1918, pp. 197-310.) ‘Bare, Miss Dororura M. A., Hon. M.B.0.U. On a new Genus of Extinct Muscardine Rodent from the Balearic Islands. (Plate I. and Text-figures 1 & Ze) eee Bouencer, G.'A., F.R.S., F.ZS. On the Madagascar Frogs of the Genus Mantidactylus Bl great sore te. Rh. att cee wth otk BREN AY. ase gars CoPEMAN, ew! S. Monckton, M.D., F.R.S., F.Z.S. Exhibition of, and remarks upon, a colony of Burrow- ime: ees onmlrimmrosen RW h. Javan anusestte oo ae fer sto se simi GemniLL, James F., M.A., M.D., D.Sc., F.Z.S. Ciliary Action in the Internal Cavities of the Cteno- phore Pleurobrachia pileus Fabr. (Text-figures 1 & 2.)... Harscuen, E. Description and exhibition of investigations into the forms assumed by drops and vortices of gelatin in various GODPAWETMIS! condeodovogboce 21020085 scospeanabbccebdddsdodoouduouddod Herron- Aven, E., F.L.S., F.R.M.S., F.Z.S. Lantern-exhibition of Arenaceous Foraminifera Wee Sai Page 209 257 304 263 vili Lanper, Miss K., F.Z.S. ‘ Description and exhibition of the method of preparing skeletons) bythe mse) Of biryPSiMen resem eee eee reeeeere Lerroy, Prof. H. M., F.Z.S., Hon. Curator of Insects. Account, illustrated by lantern-slides, of Wheat Weevil IIa VAS SEP ALIA saad Sonia vain esain a erslec ore aes aceon ems dace sree Exhibition of a series of lantern-slides from photo- graphs taken in the Zoological Gardens, Sydney, N.S. Wig OS? ok iic bin simak Be Ne Ree Renn RNC aree AR PeRoRie Ae tein aa cos fay dec Lerrrr, Dr. R. T., F.Z.S. Lantern-exhibition on Diagnosis of Helminth Infec- Lover, Sir Epmunp G., Bart., Vice-President Z.S. Notes on the Beavers at Leonardslee, 1916-1918 ...... . Mrircuett, P. Caatmers, C.B.E., M.A., LL.D., F.RB.S., F.Z.S., Seeretary to the Society. Report on the Additions to the Society’s Menagerie during the month of April, 1918 .................seeeeeeee eee Report on the Additions to the Society’s Menagerie during the month of May, 1918 ...............:.eseeeenee eee Report on the Additions to the Society’s Menagerie during the months of June, July, August, and September, Report on the Additions to the Society’s Menagerie during the month of October, 1918 ................--...:..0e. Perronievics, Dr. BRANISLAY. Comparison between the Lower Jaws of the Cyno- dont Reptiles Gomphognathus and Cynognathus. (Text- HIATT SSIES ha aedgn6 sn cdoaSooso0eOs c6- oe ais biale a fi ALT hk i : ty ° Fy tes Takacs a) Lehi rf me ; ; me i ‘ neh v) Ae ae ; whoa oe inn, cs Gi i Mh ite He A my Sra Se ae i teceleey & bis ais age jt ; ‘ar ane H ig ie EDR siti an ‘ bs ; x ent ie ot hs se a bi east ef afar A tk Beet nie _ ie oh fn aN aes i ‘ ffs bs : er Bae eis a ik ee we ti ie og.) " tok fate ties Reh as He he, a PSHE ae | . - : ee | sm os mirlag: tke set Nic M3 Lh iss ry IND EX. 1918.—Pages 197-310. [New names in clarendon type. Systematic references in italics. (z.8.%.) indicates additions to the Society’s Menagerie. | _ Alligator mississippiensis (z. s. L.), 309. Ammotragus lervia (4. s. L.), 303. Andrena fulva, 304. AVES: Exhibition of a mounted specimen of a hybrid Cockatoo, 308. Calliope calliope (z. s.u.), 304. Capra xgagrus (z. 8. L.), 304. Cercopithecus ascanius (z. 8. L.), 309. Chameleon calcaratus (z. s. L.), 304. | Connochetes albojubatus (z. s. L.), 306. | Crossorhinus jurassicus, sp. n., | 231. | | | | } | Equus kiang (z. s. u.), 307. Gecco verticillatus (z. s. u.), 507. GEOGRAPIICANL: Madagascar Frogs of the genus Man- tidactylus, 257. Hemitragus jemlaicus (z. s. u.), 307. Hypnomys, gen. n., 210. —— mahonensis, sp. n., 218. —— morpheus, sp. n., 219. Hystrix eristatus (z, s.u.), 3U7. INSECTA : Observations on a colony of burrowing Bees, exhibited, 304; On Wheat Weevil in Australia, 307. Lacerta taurica (z. s. L.), 306. Mammania: On a new genus of Extinct Muscar- dine Rodent from the Balearic Islands : structure, systematic, 209 ; the Beavers at Leonardslee, 255; The ages of Elephants, as inferred from the Molar Teeth, exhibited, 503; An abnormally coloured Red Deer, skin exhibited, 807; The ‘‘ New” Rabbit demonstration, 308. Mantidactylus ambohimitombi, sp. n., 260. Mo .usca: Ciliary action in Plewrobrachia pileus, structure, 263 ; Lantern-exhibition of Arenaceous Foraminifera, 4503. Morpnonoay. Sce StRUCTURE. Myvcastor coypus (z. s. L.), 307. Notes on Disease, x INDEX. Paleornis eyanocephala (z. s. u.), 303, PATHOLOGY. The function of Pathological states in Evolution, 237; Diagnosis of Helminth infections, 308. Pisces : On two new Hlasmobranch Fishes: systematic, 281; Account of the Freshwater Fishes of Britain, 303. Protospinacide, fam. n., 232. Protospinax, gen.n., 233. —— annectans, sp. n., 233. Python reticulatus (z. s,u.), 809. Great ReEpriuta : Comparison between the lower jaws of the Cynodont Reptiles Gompho- gnathus and Cynognathus: struc- ture, 197; On Hermaphroditism in a Lizard: structure, 223; Mada- gascar Frogs of the genus Manti- dactylus: structure, systematic, ZO On primitive known reptile: structure, 267. ; Seymouria, the most STRUCTURE. Mammarta: On a new genus of ex- tinct Muscardine Rodent from the Balearic Islands, 209. ReprintA: Comparison between the lower jaws of the Cynodont Rep- Gomphognathus and Cyno- gnathus, 197; On Hermaphro- ditism in a Lizard, 223; Mada- gascar Frogs of the genus Mazti- systematic, 257; On Seymouria, the most primitive known reptile: structure, 267. Motnuusea: Ciliary action in Piewro- brachia pileus, 263. tiles dactylus, Taurotragus oryx (z. 8. L.), 807. PRINTED BY TAYLOR AND FRANCIS, RED LION COURT, FLEBT STREET, J >: . _ - ; Gal i? | ees ae “gi | | Ba | +2 2 se | ” h i PROCEEDINGS OF THE GENERAL MEETINGS FOR SCIENTIFIC BUSINESS OF THE ZOOLOGICAL SOCIETY OF LONDON. 1918. ~ PARTS III. & IV. contTaInInG Pages 197 to 310, with 2 Puiates AND 80 TEx?-FIGURES. S mt sentan Instityg 7) FEB 17 1920 PRINTED FOR THE SOCIETY; wae’ SOLD AT ITS HOUSE IN REGENT’S PARK. LONDON : MESSRS. LONGMANS, GREEN, AND CoO., PATERNOSTER ROW. | | [Price Twelve Shillings. | az: LIST OF CONTENTS. 1918, Parrs III. & IV. (pp. 197-310). EXHIBITIONS AND NOTICES. Mr. R. I. Pococx, F.R.S., F.Z.8., Curator of Mammals. Exhibition of, and remarks upon, a series of the molar teeth of Elephants eeoeeeer tt Coo ese ee rete veers sess ee ee ee OO oe oe Mr. E. Heron-Autey, F.LS., F.R.M.S., F.Z.S. _Lantern-exhibition of Arenaceous Foraminifera Ce CC i i i er a cc ey The Szcrerary. Report on the Additions to the Society’s Menagerie during the month CEPAMIEUL LOLS rine nv ter stay eketars ene nile oy wemcia ie emer av ese toate pa oe : ee ee Se ee oe ce ts ee ee te ‘ Mr. C. Tarn Ragan, M.A., FE.R.S., F.Z.S. Account, illustrated by lantern-slides, of the Freshwater Fishes of Great Britain .« CC ee ee rr ary The Secretary, Report on the Additions to the Society’s Menagerie during the month roy Oy ea at US) ie Pease ee Olean wh Aeris ce ent NE PE ES AN Mtg ere Sen ire reins ac Lt.-Col. S. Monexton Corzman, M.D., F.R.S., F.Z.S. Exhibition of, and remarks upon, a colony of Burrowing Bees on Primrose Hill ee ee ee ewe ee PH ee oe eco esos te SO oe ee oe oe The Szcrerary. Report on the Additions to the Society’s Menagerie during the months of. June; duly, August,.and Septenfber, LOLS 7. 105. scioc0ec50 008 BoRdeAGH 1N6209ed0oRCRdAHNG oys000. ZANY) During a second visit to Mallorca in 1910 in search of ossiferous deposits a few rodent remains were obtained; the following year further researches were carried out in Menorca by means of a grant from the Trustees of the Percy Sladen Memorial Fund, and here similar remains were found to be somewhat more plentiful, occurring in several fissures in the Miocene limestone. A de- scription of the deposits from which the collection was obtained has already been published}. A first cursory examination of the specimens led me to suppose that they represented large forms of Hliomys§ or Leithia||. Since then a number of spe- cimens from Menorca have been developed from the hard matrix in which they were embedded, and all have been carefully examined, with the result that it is found that they cannot be included in any genus with which I have been able to compare them. The examples from the two islands differ considerably in size, those from Menorca being the larger, and they are probably specifically distinct: in this connection it is interesting to remember that, after the examination of a very large quantity of material, a similar variation in size was found to obtain in Myotragus 4. This seems to point to a longer period of isolation in Menorca, the most easterly and probably the first of the group to be separated from the mainland. All the remains obtained are now in the collection of the British Museum (Natural History). No complete skulls and only a few limb-bones were procured, but it will be seen from the descriptions of the specimens given below that the Balearic genus should undoubtedly be included in the Muscardinidee. The specimens to be described are intermediate in size be- tween the largest recent forms and the extinct Leithia from Malta, and show a number of points of resemblance both to the recent Hliomys and to the Maltese Leithia, but at the same time differ to an equal extent from both these genera. The * Communicated by Dr. A. SmirH Woopwarp, F.R.S., F.Z.S. + For explanation of the Plate see p. 222. @ £ Geol. Mag. [6] vol. 1. 1914, pp. 337-45. § sad. p. 100. || Proc. Zool. Soe. 1916. p. 424. See Andrews, Phil. Trans. Roy. Soc. ser. B, vol. 206, 1915, p. 301. 210 MISS DOROTHEA BATE ON A NEW GENUS range of species in neighbouring islands is always of interest, which may perhaps make it worth mentioning here the present- day distribution of Hliomys in the Balearics. Mr. Oldfield Thomas has described #. gymnesicus* from Menorca, a species smaller than, though similar in coloration to, 1. quercinus, which, in spite of this, he believes to be most nearly allied to the Southern forms. In an earlier paper ft the same author mentions that this animal is also well known in Mallorea but is said not to occur in Ibiza. Unfortunately I have not seen one from the larger island, but in the British Museum there are now several specimens from the small island of Formentera to the south-west of Ibiza, which prove to belong to the large form /#. lusitanicus which is found on the neighbouring mainland of Spain. Remains of Muscardinide are known only from European deposits, and occur from Miocene times. Hliomys itself is repre- sented by #. pomeli in the Lower Miocene of Allier, and by E. hamadryas in the Middle Miocene of La Grive St. Alban and Steinheim. Both species are of small size, and from the mandible do not show any close affinity to the remains which form the subject of this note, than which they would both appear to be already more highly specialised. In the British Museum there are two mandibular rami supposed to represent an Lliomys from the Pleistocene of Malta (B.M. 49342c and 49351)%. These are considerably more robust than in any recent member of the genus, and are found to resemble in shape the Mallorcan speci- mens and to be only slightly inferior in size, although the length of the alveolar area is considerably less. Unfortunately none of the cheek teeth ave preserved, and the formation of the rcots can- not always be satisfactorily deduced from an examination of the alveolar cavities, though in one of these specimens (B.M. 49351) it seems that in the first and second molars the posterior roots had become confluent as in the genus now to be described. These specimens seem worth mentioning as suggesting a possible exten- sion of the known distribution of the Balearic dormouse. So far as [am aware, no other rodent remains have been described from the Balearics, although so long ago as 1855 De la Marmora wrote § that he had observed indications of an ossiferous breccia in the hill of Belver near Palma, in which he had seen a bone which seemed to belong to a Lagomys or to a rabbit. The following description of the most important specimens obtained may be taken as applying to the genus so far as known at present. It is proposed that the genus be known as HyYPNnomys, gen. nov. Skull, mandible, and limb-bones as in Eliomys but more robust ; interorbital region wide and anterior portions of frontals greatly * Ann. Mag. Nat. Hist. ser. 7, vol. xi. 1903, p. 494. + Proc. Zool. Soc. 1901, .p. 41. Cat. Foss. Mamm. Brit. Mus. Pt. i. p. 225 (1885) (as Myoxus sp.). of § Mem. Accad. Se. Torino (ser. 1), vol. xxxvil. 1885, p. 59. OF EXTINCT MUSCARDINE RODENT. PAU “expanded. The infraorbital foramen opens anteriorly and the outer wall of the infraorbital canal is very robust with a wide base. The anterior palatine foramina penetrate for some distance the palatal plate of the maxille which forms the greater portion of the palate. The angle of the mandible is perforated. Dental formula i. +, pm. +, m. 3, molariform premolars and molar crowns sub-quadrate in shape with low transverse ridges. Upper molars with one large wide internal and two smaller external roots. In the first and second lower molars the two posterior roots may be confluent for the greater part of, or for their entire length; the Jast molar has two anterior and one large posterior root. Tibia and fibula joined. Skull.—The skull is represented only by some few fragmentary specimens none of which show the posterior portion, that is to say behind the frontals. An isolated and imperfect auditory bulla (B.M. M 11671) was obtained which agrees in form and in the shape and position of the meatus with the corresponding bone in Dyromys. So far as available specimens show, the skull in general resembles and may be compared with that of Hliemys, which for our present purpose will be taken in a broad sense and to include Dyromys. Even the smaller examples (those from Mallorca) are larger and comparatively, as well as actually, more robust than EZ. lusitanicus, which is the largest of the recent species of that genus. Viewed from above, the nasals are seen to be practically flat and about the same width throughout their length. The interorbital portion of the frontals is wide and smoothly flattened and is defined by sharp lateral edges; a measurement taken at the narrowest point is nearly half the antero-posterior length of the nasals in Hypnomys, whereas in H. lusitanicus it is not quite a third. Anteriorly the frontals expand rapidly by a smooth swelling and attain to a great width—about twice that of the interorbital region—where they are joined by the nasals and the nasal processes of the maxillze. This expansion is caused by the very large size of the olfactory cavities (Pl. I. fig. 14). There is a fine but distinct ridge on the dorsal aspect of the maxilla at the upper root of the zygoma from where the skull narrows rapidly to form the snout. The premaxille are robust, slightly inflated dorso-anteriorly as in Lliomys, and deep dorso-ventrally, the rostrum being stouter than in LH. lusitanicus. The infra- orbital region is not very well preserved in any of the Balearic specimens, but sufficient is shown by two or three examples to demonstrate that in this respect’ Hypnomys shows no close resemblance whatever to either a typical Murine such as Rattus or to typical Seiurines such as Seirus or Xerus. Though showing more general resemblance, this portion of the skull in the Balearic genus still differs somewhat from that of any other of the Muscardinids with which I have been able to compare it; in some respects it seems to agree with that of Leithia, though unfortunately all the anterior portions of skulls of this last in 212 MISS DOROTHEA BATE ON A NEW GENUS the British Museum are either very imperfect or else considerably erushed and distorted. The infraorbital foramen opens anteriorly and, as well as can be seen in tne type specimen of Hypnomys mahonensis (Pl. I. fig. 2), it has a greatest length of about 3 mm. and occupies a median position between the two roots of the zygomatic process of the maxilla. The lachrymal foramen shows an extension of similar length, but ovoid in form, in front of the infraorbital foramen much as in J/uscardinus, and without the lower lateral expansion seen in Hliomys. The outer wall of the infraorbital canal is very robust, broadly concave anteriorly, with a distinct outstanding point in front of its base, which is wide owing to the hinder border being produced outwards from above the first molar. The anterior palatine foramina start a short distance behind the incisors and penetrate the palatal plate of the maxille for some distance, their extent being comparable with that obtaining in Hliomys. The palate (Pl. I. fig. 1) is not completely preserved in any of the specimens, but can be seen to be wide and gently concave and chiefly composed of the palatal plate of the maxille, which extends posteriorly about as far as the hinder border of the second molar. The palatal plate of the palatines is hardly shown but can certainly have formed only an insignificant portion of the palate. Text-figure 1. Left mandibular rami of :— | A. Leithia melitensis (B.M. 49342 D), B. Hypnomys morpheus (B.M. M 11697), C. Hliomys lusitanicus (recent specimen). X 1}. Mandible—In general plan the mandible (text-fig. 1, B) is essentially as in Hliomys (text-fig. 1, C), from which it yet differs strikingly, although this difference is easier to observe than to describe. That of Hliomys may be said to have an aspect of OF EXTINCT MUSCARDINE RODENT, OB) attenuation, its posterior portion particularly being very slight and the cheek-teeth closely crowded together. This applies also to the skull, though perhaps to a lesser ‘degree. The mandible of the Balearic genus is altogether more robust, and gives the im- pression of being possibly Tess highly specialised. The angle of the jaw is per forated, and also resembles in shape that of Hliomys, but compared with this last the coronoid process originates further forward and rises more abruptly; it tapers to a slender point but is comparatively shorter and the space between it and the condyle less deepiy excavated: this last also applies to the region between the condyle and the highest point of the angle, causing the hinder portion of the jaw to be more solid owing to this comparatively greater extent of bone. The articulating surface of the condyle is strongly marked. The symphysial region and that between it and the cheek-teeth are likewise robust. The incisor extends considerably behind and rises above the cheek-teeth row, causing a marked protuberance on the out- side of the jaw at the base of the coronoid process, and the inferior dental foramen occupies a correspondingly high and backward position. Teeth.—The dental formula is tune ene as that of other of the Muscardinidee, that is to say, 1.4, pm.+,m.3. The incisors are of medium size, with the anterior SM of enamel smooth and stained the characteristic orange-yellow colour. The upper incisor originates above and just in front of the premolar; its inner surface (PI. I. fig. 10) is flat and the outer gently rounded, this being also the case in the corresponding tooth of the lower jaw. Both are considerably compressed laterally with the antero- posterior thickness much greater than the lateral width, this bein 8 nearly double in the lower teeth. Their transverse sections (Pl. I figs. 11 & 12) are more or less elliptical in shape, thus differing from those for instance of Lliomys, Glis, and Leitthia, in which the section forms practically an isosceles triangle with the anterior face as the shorter base (PI. I. fig. 13). There is naturally a corresponding difference in the shape of the worn surfaces of the teeth. As Mr. Hinton has pointed out to me, these differences in the form and proportions of the incisors are of importance as indicating probable differences in the modes of life in these various genera. It is interesting to find that an examination of the microscopic structure of the enamel in the incisors of Hypnomys seems to bear out the conclusions independently arrived at from a general study of its remains. Mr. Thornton Carter very kindly under- took the task of making this examination, and allows me to include his report of his investigations, which is as follows :— “The structure of the enamel of the incisors in the specimens from Menorea and Mallorca is identical with that of Lewhia melitensis. “The ‘pattern’ is distinctive and presents characters which would seem to place it between Sciuride and Myoxide. In Proc. Zoou. Soc.—1918, No. XVI. 16. 214 MISS DOROTHEA BATE ON A NEW GENUS longitudinal sections the enamel rods (or fibres, as Sir John Tomes designates them in his classical memoir) leave the surface of the dentine with a slight curve and then proceed outwards, slightly flexuous, at an angle of about 70° with the dentinal sur- face for about half the thickness of the enamel, where they bend sharply and abruptly to proceed in a straight course to the surface. “There is appearance of serrations of the margins such as is usually seen in the Dormice. “Thus the course of the rods is as in Myoxide, whilst their form is as in Sciuride. “In transverse section alternate groups of rods cross one another at an angle of about 120°, and when half-way through turn sharply outwards and run parallel out to the enamel surface which they reach at right angles, the pattern assumed resembling, though not identical with, that seen in a transverse section of the incisor of Hliomys.” While the palate is almost uniform in width, the rows of cheek- teeth appear curved owing to their inner borders being practically in a straight line, so that all the differences in the sizes of the teeth, especially that of the premolar, affect only the outer border of the rows, which thus have a curved outline. The plane of wear of the premolar is almost horizontal, while that of the molars lies at a considerable angle, the inner border being the higher; this character will be referred to again later. Some scarcely worn upper molars are slightly concave and their enamel ridges incline towards being cuspidate, but in most of the specimens obtained the worn surfaces of the crowns are nearly flat. The molariform upper premolar is bluntly triangular in outline and the molars subquadrate in shape, the second being very little larger and the third not much smaller than the first. In the above characters these teeth somewhat resemble those of Leithia, those of Hliomys differing markedly in the concavity and greater comparative width of their crowns. In the Balearic molars the ridges are low, and in those of aged individuals, of which a number were obtained, these become almost entirely worn away. In little-worn specimens (PI. I. fig. 1) it can be seen that in each of the upper cheek-teeth the crown is crossed by four complete and one incomplete transverse ridges, with the addition of one or more further incomplete ridges in the second and third molars. The second complete ridge in the first and second molars runs from the inner border . in an anterior direction for more than half its distance before turning to reach the outer margin. The two posterior complete ridges run more or less parallel with the hinder border of the teeth, and it is in the space left between the complete ridges that the incomplete ones occur. The inner edge of the crown surface almost invariably remains unbroken, while the outer border is cut by the valleys between the ridges. Im much worn teeth there is found a confluent valley alongside the inner enamel border of OF EXTINCT MU. CARDINE RODENT. 215 the tooth for the whole of its distance; this condition of wear is also seen for instance in Leithia, Hliomys, and Xerus. Apart from size, the upper molars of Letthza chiefly differ from those of Hypnomys in their transverse ridges being considerably higher and more sharply defined, and in the complete ones in the first and second molars originating at the postero-internal border of the crown as already described and figured by Mr. Lydekker*. Of the lower cheek-teeth the premolar is the smallest and is obtusely triangular in shape; the third molar is somewhat larger with a rounded posterior margin. although the crown has a tendency to become squarer in outline when much worn. The first and second molars are the largest of the series, almost equal in size and in shape quadrate, or with the antero-posterior length slightly greater than the width. The number of ridges appears to be much the same as in the upper cheek-teeth, though they become broken up earlier and into a greater number of incomplete ridges. In a moderately worn specimen (B.M. M 11674, Pl. I. fig. 6) the first and second molars seem to have three complete ridges, two distinct incomplete ones running half-way across the crown from opposite sides and a shorter one coming in from the antero-external corner, while the antero-internal area is broken up into several rather indistinct loops. The third molar shows four complete ridges and two small accessory ones. In the case of aged individuals the confluent worn surface is of course along the external border of the crown, it being on the internal side in the upper cheek-teeth. In less worn specimens this external enamel border is interrupted at two points, and the enamel between and on either side of these channels, owing to its being slightly folded over, is at this stage of wear more massive than in other parts of the ridges. The number, position, and conformation of the roots of the cheek-teeth in rodents form a subject of considerable interest and importance, and it is one that has received a good deal of atten- tion from investigators, notably Schlosser f and, later, Dr. Forsyth Major{. The specimens under discussion are no exception in this respect, for their molar roots are unlike those of any Pleisto- cene or recent genus with which I have been able to compare them with the single exception of Zetthia, and that only in the ease of the upper molars. It may be mentioned that I have not found this character previously noted in the descriptions of the Maltese genus. The alveolar formula can be most easily realised by reference to the accompanying text-figure (text-fig. 2), but at the same time it should be borne in mind that such a formula alone is of very little value for purpoess of comparison. The present examples are a case in point, as, for instance, the first and second upper molars of Hliomys and Gilis are three-rooted, as in * Proc. Zool. Soc. 1895, pp. 861-3, text-fig. 1. + ‘Paleontographica, Band xxxi. 1885. + See, for instance, the following: “On Fossil Dormice,” Geol. Mag. Nov. 1899, p. 492, and “On some Miocene Squirrels,” Proc. Zool. Soc. 1898, pp. ee i a ~ 216 MISS DOROTHEA BATE ON A NEW GENUS Hypnomys and Leithia, but an examination of the roots them- selves show them to be essentially different. In Hypnomys the upper premolar has three long and rather stout roots, which terminate in blunt rounded ends(B.M. M 11658, Pl. I. fig. 3). The anterior one takes a forward direction and is the shortest of the three, the other two project in a parallel direction from the hinder border of the tooth and may be con- fluent for a varying distance, but apparently not for more than half their length. This description is based on examples of Hypnomys mahonensis, but the alveolus in a Mallorcan specimen indicates a similar formation. Unfortunately there has been no opportunity of examining any milk-teeth in the case of either this genus or Leithia. Text-figure 2. A. B: Sens cae 3 \ ITt g gue & [RILe felt i eh Sat = Seb B6 2) 6e@ z OS 3b M72 met ae 28 Sie bie nee Sh a UValveoi. t.alveoh. U.alveolt. L.alveoli Diagram of alveoli of cheek-teeth of A. Hypnomys and B. Leithia. The upper molars each have three roots, one large internal and two small external ones, a number commonly found in many rodents. The distinctive feature of the Balearic teeth lies in the construction of the large internal roots: in Hliomys, Gis, and also in other forms such as Xerws and Sciwrus, which have the same alveolar formula, these are single, rather flattened conical roots projecting from the centre of the border of the crown which they support. In Hypnomys the internal root is quite different, this being clearly portrayed in the accompanying illustrations. Fig. 3 (Pl. I.) shows the latero-internal view of the first and second molars of H. mahonensis: it will be seen that there is a slight constriction at the base of the crown where the enamel ends, and from there the confluent root continues practically of the same size for its whole length, which is a little less than twice the antero-posterior length of the crown-surface. In the figured specimen the first molar measures 4 mm. from the crown-surface to the tip of the root, while the antero-posterior length of the crown is very little more than 2mm. In the second molar the root is very slightly shorter and not rounded at its apex, but this way perhaps be partly due to damage in developing the specimen. The internal root of the third molar is exposed in the type OF EXTINCT MUSCARDINE RODENT. 217 specimen of 1, mahonensis (B.M. M 11657), in which it is seen to be similar to that of the other two. In some specimens there is a slight groove along the centre, indicating the compound nature of the roots ; the ends are ciosed in all examples examined. The slight intero-external width is well shown in the section (B.M. M 11661, Pl. I. fig. 4) and in the posterior view of the second upper molar (B.M. M 11660, Pl. I. fig. 5), in which it can also be seen that there is a certain amount of curvature in the direction of the compound roots. They are considerably longer than the external roots, although, owing to the slope of the crowns, they do not penetrate much deeper into the alveolar cavity. As already mentioned, the upper molar roots of Leithia are sinilar to those of Hypnomys, the only other genus, among many examined, showing a closely similar condition of root structure 1s Lrechomys. In the British Museum there are two fragments of the upper jaw of 17. platyceps (B.M. M 1627) from the Phos- phorites of Caylux, containing the premolar and first molar, the roots of the latter being as in Hypnomys except that the broail inner root is perhaps not quite so wide compared with the crown. It must be mentioned that in 77echomys the roots of the premolar are the same as in the molars, which is of course not the case in either Leithia or the Balearic genus. The molar roots of Theridoniys are somewhat similar but are accompanied by much more hypsodont crowns. ‘The roots of the lower cheek-teeth of Zypnomys (B.M. M 11673, Pl. I. fig. 7) show a very considerable amount of variation both as regards their length and conformation. The premolar may perhaps be said to have two roots, but these are confluent for the greater part of their considerable length, diverging at a vary- ing but never very great distance from their apices, the antevior of which is slightly the longer of the two. The upper, posterior portion of the root is wide and flattened, being very evidently the result of the fusion of two roots. In some specimens (as in B.M. M 11678) there are clearly three confluent roots. In the first and second molars the two anterior roots are usually long, equal in size, and separate though not very widely divergent. In the posterior roots the length and antero-posterior thickness are about the same as in the anterior pair, so that viewed laterally little or no difference is observable (PI. I. fig. 7). But viewed from behind they are seen to be confluent transversely for either the whole or three-fourths of their length (PI. I. figs. 8, 9, BLM. M 11675-6); in the latter case the stout terminal portions of the roots may diverge considerably. The resemblance to Hypnomys seen in the roots of the upper molars of Leithia does not hold good for those of the lower jaw, for in the Maltese genns the first and second molars each have four roots, entirely separate from each other for their entire length. In Trechomys, however, the lower molar roots seem to agree with those of the Balearic genus with the possible exception of the 218 MISS DOROTHEA BATE ON A NEW GENUS third molar. Schlosser gives the number of roots for this tooth as three, but judging from the alveolus of a specimen of 7’. platyceps in the British Museum (M1627) it appears that there may some- times be two large, transverse roots only. The last lower molar in Hypnomys has three roots, two anterior slender ones and a large, backwardly projecting posterior one. This condition is very similar to that obtaining in the correspond- ing tooth of Letthia and the recent Hliomys, though in the latter there is a more marked constriction immediately below the crown. Limb-bones.—Very little of the skeleton was obtained, but a few femora, a tibia, and fragmentary portions of humeri and other bones, chiefly from a Mallorcan cave-deposit, show characters which also indicate that the genus should be included in the Muscardinide. The ulna is very similar to that of Hliomys, as is also the femur, except that the third trochanter seems to be slightly less prominent and less sharply separated from the great trochanter. As contrasted with the Hystricide, Sciuride, and Anomaluridee, which have the tibia and fibula free, a charac- teristic of the Muride and Muscardinide is the joining of these two bones for a third or more of their distal portions. It may be worth noting that in Rattws (Hpimys), for instance, the fibula at its distal: extremity is once more separated though closely adpressed to the tibia. On the other hand, in Eliomys quercinus the tibia and fibula continue completely ankylosed at their distal ends, and it is with this latter that the Balearic specimens agree, as Letthia likewise does in this respect. ‘These bones are joined for more than a third of their total length in the three last- mentioned genera. In Hypnomys the tibia isa straighter bone with a less well-developed cnemial crest than in Hliomys. The above are the chief characters of all the Balearic specimens, and it will only be necessary to add a brief note and a few measurements in the two species from the different islands. The species from Menorca may be named HyPNOMYS MAHONENSIS, Sp. n., and regarded as the type species of the genus, distinguished from the Mallorcan species by its greater size and different. habitat. Further differences would probably be apparent were a larger amount of material available. All the specimens were obtained from-fissures in the Miocene limestone, and were in one or two instances associated with remains of J/yotragus and Tesiudo gymnesicus. Some imperfect lacertilian jaws also occurred, and these have been very kindly examined by Mr. G. A. Boulenger, F.R.S.: they prove to be those of a Lacerta of the viridis-ocellata group and a species of Chalcides. Although representatives of both these occur commonly in the Mediterranean region, neither are found in Mallorca or Menorca at the present day. Owing to the fragmentary state of the specimens not many OF EXTINCT MUSCARDINE RODENT. 219 measurements can be given, but the following are afew. The length of the nasalsis about 18 mm. in the single example in which these bones are completely preserved, and the interorbital width of the frontals is 8mm. ‘The base of the outer wall of the infraorbital canal measures 6 mm., and the incisive foramina are approximately 8 mm. in length. In the type specimen (PI. I. fig. 1) the complete row of left upper cheek-teeth is almost 10 mm. in length, this measurement being 14 mm. in a corresponding example of Zeithia, and barely 7 mm, in one of Eliomys lusitanicus. In H. mahonensis the width of the palate between the first molars is not quite 6 mm., in Leithia it is little more, being 6°5 mm. The length of the lower cheek-teeth series is about 10 mm. ; as already mentioned the length of their roots is very variable: in one specimen having teeth with moderately worn crowns (B.M. M 11673, Pl. I. fig. 7) the first molar has a crown-width of 2°5 mm. with a root-length (measured from the crown-surface to root-tip) of almost 5mm. In the third molar in the same specimen the greatest length of root is 3 mm., the large posterior root attaining an antero-posterior width of 1:5 mm., while the antero-posterior length of the crown is 2°5 mm. In an example of a left lower second molar (B.M. M 11676, PI. I. fig. 9) with a less worn crown than the above the crown-width is 2 mm., and the greatest root-length 3 mm. It is proposed that the species from Mallorca be known as Hypnomys MORPHEUS, Sp. N., characterised by its smaller size and different habitat from HT, mahonensis. The few specimens of jaws and limb-bones by which it is represented were obtained from cave-deposits in Mallorca, and were found associated with remains of MWyotragus, and in one case with afew mandibular rami and limb-bones of Apodemus, which still occurs plentifully in the island. In size it appears to agree with the larger forms of Glis. The type speci- mens (B.M. M 11695), consisting of the anterior portion of the skull with the incisors and right molars and two mandibular rami, are believed to have been associated and fell apart on being separated from the earthy matrix in which they were preserved. The base of the outer wall of the infraorbital canal measures 5 mm., and the antero-posterior length of the molar row is 6 mm. The length of the lower cheek-teeth series is 8mm. In the upper incisor (B.M. M 11696) shown in fig. 10 (Pl. I.) the antero- posterior width is 2°5 mm. while the thickness is 1°5 mm.; in a specimen of the lower incisor the antero-posterior width is 2mm., with a thickness of barely more than 1 mm. The greatest length of a right tibia, wanting its proximal epiphysis, is 41 mm., the distal 18 mm. of which are joined to the fibula. A femur has a total length of 55 mm., that of a right ulna being 36 mm. bo bo =) MISS DOROTHEA BATE ON A NEW GENUS Summary and Conclusions. The above description may be very briefly summarised as follows. Ilypnomys is represented by two species known by remains from the two largest islands of the Balearic group and is consideied to belong to the Muscardinid, though seeming to be a very distinct form not closely related to any other at present known. Its dental and osteological characters so far observed not only seem to show that //ypnomys belongs to the Muscardinide but also appear to afford further support to the opinion, now very generally held, that this group cannot be included in either the so-called Sciuromorpha or Myomorpha and lending additional weight to the argument against employing these terms. This seems to hold good also for the modern representatives which have been briefly described by Mr. Miller* as “... mostly arboreal animals with habits and aspect somewhat intermediate between mice and squirrels. . . .” The Balearic genus may be compared with the recent Hliomys and the extinct Leithia trom the Pleistocene of Malta. It agrees with the former in general plan of skull, lower jaw, and limb- bones, and it may be noted that there is also a perforation in the angle ‘of the lower jaw. It differs in a number of points, among which the following may be cited :—In the pattern of the molar crowns, which are very slightly concave and lack the marginal cusps, both distinctive characteristics of Hliomys. In Hypnomys the worn surfaces of the molars are subquadrate in shape, whereas in the recent genus the width is distinctly greater than the antero- -posterior length; the alveolar formula differs in the two genera, and the large i inner root in the upper molars of Zypnomys is quite distinctive. This root-structure was evidently attained by a process of simply filling up the space between two parallel roots, whereas the single conical root seen in the Sciuride and others would seem to be arrived at by the drawing together of the apices of the two roots with a similar filling up of the intervening space. It would be interesting could one arrive at a reasonable hypothesis to account for this root-formation in Hypnomys and Leithia, for presumably it must have been acquired to meet a special stress or strain consequent on some peculiarity of diet o1 mode of life. Hypnomys agrees with Leithia in its squared molars and in the large, confluent and single inner roots of the upper molars, but differences are seen in the former having a perforation in the angle of the Jaw, which is also of a different shape (see text-fig. 1), in the crown pattern of the molars, much lower enamel ridges, and in the roots of the lower molars. It has also been noted that in the roots of both upper and lower molars, but not premolars, Hypnomys shows a striking resemblance to Zrechomys. However, it is not for a moment * «Qat. Mammals of West. Europe,’ London 1912, p. 549. OF EXTINCT MUSCARDINE RODENT. 221 suggested that this similarity, which is apparently unaccompanied by other points of resemblance, indicates any close aflinity. On the contrary, 1t would seem that these three genera each exhibit in this character what would have been a stage, and that a very early one, in the history of the evolution from the low-crowned four-rooted towards the hypsodont and rootless or semi-rootless molar. The cheek-teeth of Zheridomys also seem to suggest the possibility of this result being attained without the necessity of including a stage having a large conical inner root in the upper molars accompanied by a somewhat triangular-shaped crown, as seen in some of the Sciuride (Xerus for instance) and which Dr. Forsyth Major has fully described in his invaluable paper on the Miocene Squirrels *. Hypnomys is an interesting addition to the extinct fauna of the Balearics so far known by Myotragus and Testudo gymnesicus, both forms totally distinct from the present-day fauna of the islands. Owing to the small amount of material available, the question as to the precise age of these Balearic déposits and their contents seems a difficult, if not impossible, one to answer at present. Lately this matter has been the subject of some interesting remarks by Prof. M. Bouley, who seems inclined to consider the deposits of earlier age than Pleistocene. Seeming to support this view are the absence of human remains and the character of the chief remains found, 7. e. Myotragus, Hypnoms ys, and a giant Testudo. ‘The occurrence of remains of this last in the limestone fissures of Menorca certainly suggests that there must have been great changes of climate and vegetation, and that there have been comenileralills alterations in the land surface is indicated by extensive stretches of sheets of stalagmite now exposed on the weathered surface of the Miocene limestone in both Mallorea and Menorea. On the other hand, it should be realised that not much weight should be placed on the absence of human remains owing to the fact that not a single one of the ossiferous deposits was found to be in an undisturbed condition, all the upper layers in which such remains might be expected to occur having been entirely destroyed. Another point to be borne in mind is that in the Mediterranean region several species now extinct have been proved to have per- sisted until the time of man’s occupancy of these particular areas. The well-known Prolagus, remains of which were found in Neolithic settlements in Corsica by Dr. Forsyth Major, is a case in point. Another somewhat similar example is that of a small deer, Anaglochis, whose remains occur abundantly in some of the cave-deposits of Crete, while a number of its antlers were found by Sir Arthur Evans in a shrine in the famous Minoan Palace of Knossos. I should like to take this opportunity of expressing my grateful thanks to the Trustees of the Percy Sladen Memorial Fund for * Proc. Zool. Soc. 1893, pp. 179-214. + ‘L’Authropologie,’ tome xxviii. (1917) pp. 160-3. 222 A NEW GENUS OF EXTINCT MUSCARDINE RODENT, enabling me to visit Menorca. Also to Dr. A. Smith Woodward, F.R.S., for continued kindness in giving me every facility for working in the Geological Department of the British Museum (Nat. Hist.), to Mv. M. A. C. Hinton for kind advice and for looking over some of my material, and to Mr. J. Thornton Carter for his valuable investigations into the enamel structure in the teeth of Hypnomys and other genera. EXPLANATION OF PLATE I. Fig. 1. Hypnomys mahonensis. Type-specimen (B.M. M 11657). Palate showing 2. 3. Se Sd Sx 9 Do. Do. Do. Do. Do. Do. Do. , Do. 10. H. morpheus. Right upper incisor (B.M. M 11696), inner view. X 3. the left premolar and molars and right M!. x 4. Side view of same specimen showing anteorbital region. 3. Lateral view of right upper premolar and Ist and 2nd molars, showing the large confluent roots of the latter (13.M. M 11658). x 3. Transverse section of left M! (B.M. M11661). x 4. Posterior view of right M2 (B.M.M 11660). x 4. Crown view of right lower molars (B.M. M 11674). x 4. Lateral inner view of right lower cheek-tecth (B.M. M 11678). x3. Right My. (B.M. M 11675) showing posterior roots. X 4. Left’ Me (B.M. M 11676) showing posterior roots. X 4. ll. H. mahonensis. ‘Transverse section of upper incisor (B.M. M11662). x 4. 12. Do. Transverse section of lower incisor (B.M. M11677). x 4. 13, Leithia melitensis. Transverse section of upper incisor (B.M. M 49345 a). x 4. 14. H. mahonensis. Dorsal view of interorbital region of skull (B.M. M 11659). x 2. ON HERMAPHRODITISM IN A LIZARD, 223 12. A Case of Hermaphroditism in a Lizard, Lacerta viridis. By Nort Tayter, B.Se. (Lond.).* (From the Zoo- logical Department, University of London, University College.) [Received April 23, 1918: Read May 28, 1918. ] (Text-figures 1-3.) The specimen, the urogenital system of which is described in the following pages, was placed in my hands by Prof. J. P. Hill, F¥.R.S. It turned up in the course of class-work in the Senior Laboratory in the College, and its abnormal condition being observed, it was fixed in corrosive sublimate and preserved for detailed examination. The specimen presents certain features of interest which, it is believed, are worthy of being placed on record. I wish to express my thanks to Prof. Hill for his advice and assistance in the preparation of these pages. I. Descriptive. a. General Morphology. When this specimen came into my hands, it was in a partly dissected condition, the greater portion of the abdominal viscera having been removed. The Fat Bodies were present and well developed, the right being rather larger than the left. They are not represented, however, in text-fig. 1, which gives a general view of the urogenital system, since i situ they obscured the more anterior portions of the oviducts. The testes (text-fig. 1, R.7’. and L.7’.) were well developed and suspended in the folds of the longitudinal mesorchia (J/es.). The right was placed somewhat more anteriorly and was rather larger than the left, the dimensions of the former being about ‘9 cm. x ‘4 em., and of the latter *65 em. x °3 cm. Both gonads seem normal in shape apart from the remarkable stalked outgrowths on each (Ov.). These on section were found to contain ova, and the gonads may therefore properly he designated ovotestes. The right gonad, it will be seen, possessed two of these spherical ovarian appendages, each joined to the dorso-lateral border of the testicular portion of the organ by a well-marked stalk; the more anterior was further sub-divided into two by a median constriction. : The left gonad also possessed two outgrowths, the surface of the larger being subdivided into five or six hemispherical pro- jections. The epididymes were well developed (Z.Zp., R.Kp.) * Communicated by Prof. J. P. H1xn, D.Se., F.R.S., F.Z.S8. ° ie) i) B.Lgq. Bi. d.aort. L.Cop. L.Ep. LF |. M.D. Ing. Tbe ie Lv. MR. NOEL TAYLER ON Text-fi gure 1. Lacerta viridis: dissection of a hermaphrodite animal. Explanation of the lettering. Broad Ligament.. Bladder. Doreal Aorta. Left Copulatory Organ. Left Epididyinis. Lett Funnel. Lett Oviduct. Lung. Left Testis. Liver. Mes. Ov. R.Cop. R.Ep. RAK. RT. Mesorchium. Ovary. Right Copulatory Organ. Right Epididymis. Right Kidney. Muscular Band. Right Oviduct. Right Testis. Rectum. Spleen. HERMAPILRODITISM IN A LIZARD. 225 ‘and situated in the broad ligament parallel to but separate from the testes. They were not attached, as is normally the case, to the inner border of the testes, and vasa efferentia were conse- quently absent. Posteriorly, the epididymes passed into the vasa deferentia, and these, having united with the ureters, opened into the posterior division of the cloaca by the urogenital papillee. The two kidneys were apparently normal, each consisting of an anterior and posterior lobe (in the figure, only the right kidney, &.X., is indicated by reference letters). The copulatory organs (2. Cop., L. oes) were present as in the normal male lizard. The oviducts (?.12.D:, LZ.M.D.) were developed for about a third of their lengths. Hach opened into the body-cavity by a well-developed funnel (only the left, Z.4U., is indicated by reference letters in the figure), and behind that was continued into the duct, the plaited glandular walls of which are seen in the outer border of the broad ligament (B.Lg.). The right oviduct attained the greater complexity as in the normal female. Passing down. from the posterior tip of the ecelomic funnel on each side, on the extreme outer border of the broad lgament was a narrow but well defined ribbon-like muscular band which continued right back on each side to the cloaca. Similar bands, which were at first taken for the oviducts, were referred to by Howes (5) as the round ligaments, and he thus describes them in his specimen : ‘‘ From this (the oviducal aperture) there passed back a ribbon-shaped muscular band which skirted the free edge of the broad ligament, remindful of the round ligament of mammalian anatomy. This structure was wholly absent on the side destitute of an oviducal vestige, as indeed it is in the normal male. Its development is correlative with that of the oviduct.” b, Histology. Transverse sections were made of the gonads and stained with hematoxylin and eosin. The main body of each gonad was found to consist of normal testicular tissue, 7. e. seminiferous tubules with an interstitial stroma, the lining cells being in active mitotic division (text-fig. 2, s.t.). The stalked outgrowths were found to consist of ovarian tissue, the bulb-like extremities containing large and fully-grown ova. A section of the gonad through the nuelear plane of the most anterior ovum is somewhat diagrammatically represented in text-fig. 2. The large yolk-laden ovum (ov.) is, it will be seen, surrounded by the relatively thin follicular epithelium (/oll. ep.), outside this is a fibrous layer continuous with that sheathing the testicular portion of the gonad. In the stalk region all the normal histological elements of the ovary are represented. Outside is a layer of cubical epithelial cells continuous with the peritoneal epithelium, while the main mass of the stalk is formed of a loose stroma of connective tissue, contained in which 226 MR. NOEL TAYLER ON are numbers of young follicles of various ages, the youngest being nearest to the testis. The connective-tissue body of the stalk is confluent with the tunica albuginea of the testicular portion of the gonad, which is somewhat thickened in the region of junction. The sections of the oviducts revealed in their anterior portions a typical structure. They are lined with a well developed ciliated and glandular epithelium, the lumen of the duct being filled with the coagulated secretion of the gland-cells. Sperma- tozoa were not detected. Text-figure 2. Lacerta viridis, hermaphrodite animal: sections through gonad. ov.; ovuin. foll. ep.; follicular epithelium. s.t.; testicular stroma. The appearance of the epididymis was quite normal, but no - spermatozoa were found in the lumen of the vas deferens, and examination of the sections failed to reveal the presence of vasa efterentia through which the spermatozoa normally pass from gonad to epididymis. o « HERMAPHRODITISM IN A LIZARD. DONT In the dissected specimen two or three fine tubule-like filaments were seen to pass from the posterior ends of the oviducts to the anterior extremities of the corresponding epididymes ; these were best marked on the left-hand side (see text-fig. 1). These filaments were carefully examined in the sections. The epi- thelial lining of the oviduct was found to end posteriorly in a cul-de-sac, as did that of the epididymis anteriorly. The “filaments” in section appeared as actual tubular passages devoid of any epithelial lining and running in the substance of the broad ligament. They commenced at the extreme anterior tip of the epididymis, and while two of them ended blindly, the third ran up as far as the posterior extremity of the oviduct, its lumen being continuous with the spaces in the mesentery in which were contained the glandular portion of the oviduct. Text-figure 3. Lacerta viridis, hermaphrodite animal: section through kidney. kid.; kidney tissue. foll.ep.; follicular epithelium. thee. foll.; theca folliculi. The morphological interpretation of these spaces would seem a problem of some difficulty. Being devoid of epithelial lining and making no connection with the lumen of the epididymis, one would hardly seem justified in regarding them as rete tubules proper, while the close relationship of one of them with the oviduct also seems anomalous, on this view. The condition which Howes (5) describes in one of his specimens seems of some interest in this connection. ‘In one instance,” he says, ‘“‘I discovered an interesting modification of the condition recorded by Leydig. There was buried up in the 228 MR. NOEL TAYLER ON peritoneum in a line with the head of the epididymis a delicate filament which, while it answered in every respect to the rudiment described by him, instead of ending abruptly and blindly became suddenly enlarged, opening into the body-cavity by a wide-mouthed funnel-shaped extremity, identical with that of the oviduct, and lined by a ciliated epithelium.” This without doubt seems the description of a vestigial oviduct, yet, posteriorly, according to his figure, it appears to arise from the anterior tip of the epididymis. Unfortunately he does not seem to have investigated the precise nature of its relations to this organ. The sections through the kidneys reveal the presence on the dorsal portion of one of them of an embedded mass of almost fully grown ova. Text-fig. 3 is a semi-diagrammatic representation of one of the sections in which five ova occur. It will be seen that the mass of ova lies actually embedded within the kidney tissue (Aid.). Hach ovum is surrounded by a layer of follicular cells (foll. ep.), while externally to this and separating it from the kidney substance is a thin fibrous layer (thee. foll.) presum- ably representing the theca folliculi. Il. Discusston. No instance of complete hermaphroditism in the Lacertilia seems yet to have been put upon record, though cases of the more or less complete developmeut of the Miillerian Ducts in adult male lizards have been described. Leydig in 1872 (7) described the persistence in the males of Lacerta agilis of the Millerian Ducts as small blind and con- voluted tubules, while Braun in 1877 (2) noted the development of rudimentary Miillerian Ducts in the young male of the same species, making no mention, however, of its presence in the adult form. In 1887 Howes (5) published a brief but important paper, “On the vestigial structures of the reproductive apparatus in the male of ne Green Lizard” (Lacerta virdis). One of his specimens was a male lizard in which both the oviducts were all but fully aeons while in another the oviduct was fully developed on one side. In thirteen out of twenty-five specimens examined certain segments of the oviduct were well developed, the other portions being only represented as delicate filaments, thus giving a series of conditions analogous to those described by Matthews for the male toad. In 1893, Hill (4) published an account of the persistence of vestigial Miillerian Ducts in the full-grown male of an Australian lizard, Amphibolurus muricatus ; while two years later, in 1895, Jaquet (6) described the presence of Miillerian Ducts identical with those of the normal female in an adult individual of Lacerta agilis. HERMAPHRODITISM IN A LIZARD, 229 All the above mentioned cases are, it will be noted, pre- dominantly male, indeed as far as their gonads are concerned wholly male, for in no case is any reference made to the presence of ova or ovarian tissue. In this respect the specimen described in the present paper stands in striking contrast to previously described cases; more- over, while it is distinguished by the presence of well-marked ovotestes, it must have been physiologically sterile. Among lower forms the occurrence of well-developed Miillerian Ducts seems often to be accompanied by the existence of an ovotestis. Cases of this kind have been described by Marshall in the Frog (8), but Fantham (3) seems to have been the first to record a case of true hermaphroditism in the Reptilia. The specimen of Testudo greca described by him possessed well- developed oviducts, the lumen of each being continuous through- out. Of the two gonads the right was a typical testis, on the ventral surface of the left however was a “conspicuous yellow egg.” On section another was found devoloping in its proximity. while ‘“‘a few groups of bodies resembling developing ‘ ovarian ova’ were seen scattered in separate groups (follicles) among otherwise testicular tissue, more especially near the periphery of the anterior portion of the gonad.” Epididymes, vasa efferentia and vasa deferentia were present as in normal specimens, the former being rather large. It seems a point worthy of note that the development of the oviducts in the cases referred to above, viz., those of Howes, Till, and Jaquet, is much more complete than in the subject of the present paper; in all these three cases the oviducts were developed throughout their whole length and opened into the cloaca, yet in none of these cases is any mention made of the presence of ova or ovarian tissue. In the present specimen, on the contrary, numerous ova occur, though only the anterior thirds of the two oviducts are fully developed, Literature referred to. 1. Bourns, A. G.—‘‘ On certain abnormalities in the Common Frog; 1. The occurrence of an ovotestis.” Q.J.M.S. xxiv. 2. Braun.— Das urinogenital Syst. der einheimischen Rep- tilien.” Arbeit. aus dem zool.-zootomisch. Instit. Wiirzburg, vol. iv., 1877-8. 3. Fanruam., H. B.—‘‘ On Hermaphroditism and Vestigial Structures in the Reproductive Organs of ZVestudo graca.” Ann. Mag. Nat. Hist. xvi. 1905, p. 120. 4. Hi, J. P.—“‘ Note on the presence of Vestigial Miillerian Ducts in a full-grown male lizard (Amphibolurus muricatus).” Proc. Linn. Soc. N.S.W. vol. viii. (Series 2nd), Sept. 27th, 1893. Proc. Zoou. Soc.—1918, No. X VEL. ee 1230 ON HERMAPHRODITISM IN A LIZARD. 5. Howrs, G. B.—“ On the Vestigial Structures of the Repro- ductive Apparatus in the Male of the Green Lizard.” Journ, Anat. & Phys. xxi. pp. 185-9, 1887. 6. Jaquer, M., (1895).—‘“* Note sur un cas d’hermaphroditisme incomplet observé chez le Lacerta agilis.’ Bibliogr. Anat, (Paris—Nancy) iii. p. 267. 7. Leypia.— Die in Deutschland lebenden Arten der Saurier.” Tubingen, 1872. 8. Marsuatyt, A. Mrtnes.—‘‘On certain abnormalities of the Reproductive Apparatus of the Frog.” Journ. Anat. & Phys. xvii. pp. 121-144. PZ.S. 1919. WOODWARD, PLL. Huth imp. lth. et 1 a Giaweadarated del CROSSORHINUS JURASSICUS. 3. PROTOSPINAK ANNECTANS. ON TWO NEW ELASMOBRANCH FISIIES. 231 13. On two new Elasmobranch Fishes (Crossorhinus juras- sicus, sp. nov., and Protospinaw annectans, gen. et sp. nov.) from the Upper Jurassic Lithographic Stone of Bavaria. ine Senor Smita Woopwarp, LL.D., DIBA, Wea [Received May 23, 1918: Read June 11, 1918.] (Plate I.) Most of the modern groups of Elasmobranch fishes seem to have arisen during the Cretaceous period, but some are of still older date, and a few interesting types are represented by well-’ preserved fossils in the Upper Jurassic lithographic stone of Bavaria, Wirtemberg, and france. Two remarkable new examples of these early forerunners of the existing fauna have lately been identified in the British Museum, one apparently indistinguishable from an existing genus, Orossorimus (ov Orecto- lobus), the other evidently of a new genus and family closely related to the Spinacidee. Family CROSSORHINIDAK, CROSSORHINUS JURASSICUS, Sp. n. (PI. I. fig. 1.) Specific Characters.— Head gently rounded in front; length of -head and trunk about equal to that of the tail. Three pairs of fringing dermal lappets, all undivided, the first extending along the Sides of the front half of the head, the next pair diminutive, and the third pair largest, extending along the sides of the branchial region. Pectoral fins rounded, relatively large, ex- tending nearly as far back as the origin of the pelvic fins, which are also rounded and about two-thirds as wide as the pectorals. Dorsal fins rather small and apparently nearly equal in size; the first dorsal arising opposite the hinder limit of the pelvic fins* the second ending in “advance of the much smaller anal fin, which is close to the lower lobe of the caudal. Body and fins covered with very fine shagreen, of which some granules between the pectoral fins have a fluted sculpture. Description of ype Specimen.—The fossil, which is shown of the natural size in Pl. J. fig. 1, is exposed in its anterior half from below, in its caudal half from the side. The snout is short and bluntly rounded, and the rami of the jaws are vaguely seen, meeting in an acute angle at the symphysis, where there are remains of a cluster of very slender, smooth, pointed teeth. ‘The branchial region is relatively long, but the branchial arches are even more obscured by the crushed shagreen than the jaws. A single 17* 232 DR. A, SMITH WOODWARD ON i pair of large dermal lappets (IIL), widest in front and gradually narrowing backwards, extends along the whole length of the bran- chial region, Another pair of minute simple lappets (II) is well seen just in front of this, and the mode of staining of the fossil suggests that there is a long and narrow fringe of skin (1) along each side of the rostral region. The vertebral centra are much constricted and smooth, but where broken they seem to exhibit traces of some secondary calcification round the primitive double- cone. Their arches are not distinguishable, but the comparative shortness of the centra in the front part of the caudal region evidently results from diplospondyly. The large pectoral fins are remarkably rounded, slightly longer than wide, and the stout basal cartilages do not extend more than half-way towards the distal margin. The long unjointed proximal radial cartilages are well seen in the left pectoral. The tapering ascending parts of the pectoral arch are crushed backwards. The pelvic fins, which are much longer than wide, are supported in their basal half by very stout radial cartilages ranged along the basipterygium, which is not produced into claspers. ‘The individual represented is therefore female. The two dorsal fins are crushed downwards to the left side of the fossil, and seem to have been nearly, equal in size; but the parts projecting beyond the edge of the tail probably represent only their apical halves. The first dorsal, which is rather fragmentary, arises just behind the end of the pelvic fins, while the second must have been completely in advance of the anal. The anal fin is relatively small, short, and rounded, and close to the lower lobe of the much extended caudal fin. The lower lobe of the latter is clearly notched near its distal end. The head, trunk, and fins are completely covered with very fine shagreen. Most of the granules appear to be flat and smooth, but some are pointed, and a few on the back of the trunk between the pectoral fins are both pointed and slightly enlarged and coarsely fluted. Affinities —So far as preserved, there is nothing in the fossil thus described to separate it from the existing genus Crossorhinus, but it is distinguished from all known species* by the simplicity of the dermal lappets fringing the head, and by the relatively large size of the pectoral fins. Family PROTOSPINACIDAS, nov. Body depressed, but base of pectoral fins not produced forwards. — Vertebral centra well calcified (probably tectospondylic). Radial cartilages of paired fins not extending to the margin; two dorsal fins on the tail, each with an anterior spine; anal fin present. * Compare C. Tate Regan, P. Z. S. 1908. pp. 354-357, pl. xi. fig. 2, pl. xii. fig. 2; also Ann. & Mag. Nat. Hist. [8] vol. iii. (1909), p. 529. J. Douglas Ogilby & A, R. McCulloch, Journ. Roy. Soc. N.S. Wales, vol. xlii. (1908), pp. 269-280, pl. xlii., pl. xlii. fig. 1. For skeleton see also W. A. Haswell, Proc. Linn. Soc. N. S. Wales, vol. ix. (1884), pp. 92-98, pl. 1. figs. 6-8, pl. ii. fig. 13. TWO NEW ELASMOBRANCH FISHES. 233 Genus PROTOSPINAX, nov. Snout short and obtusely rounded. Teeth small, compressed toa sharp edge. Pectoral fins extending as far backwards as the pelvic pair; dorsal fin-spines large, laterally compressed, and smooth, the first inserted opposite the pelvic fins; anal fin very small, close to the elongate-ovoid caudal, which is not notched. Shagreen dense and fine, none enlarged; lateral line supported by a series of calcified ringlets. PROTOSPINAX ANNECTANS, sp. n. (PI. I. figs. 2, 3.) Specific Characters.—Attaining a length of about a metre. Length of cranium shghtly less than one-fifth, length of caudal fin about one-sixth of the total length. Teeth smooth and lozenge-shaped, their sharp-edged crown sometimes with a prominent middle point. Antero-posterior measurement of pectoral fin about equal to the length of the cranium, and nearly twice as great as the length of the pelvic basipterygium. Dorsal fins about equal in size, the first arising slightly in advance of the middle of the fish. Description of Type Specimen.—The fossil, which is shown of one-sixth the natural size in Pl. I, fig. 2, is very fragmentary, but there are definite points of contact between the pieces of rock in which it is contained, and most of it is preserved in counterpart, so that its general shape and proportions are recog- nisable. The head and trunk are seen directly from above, while the greater part of the tail is exposed im side-view. ‘he edges of the head and fins are sharply outlined by fine dense shagreen, while the distinctness of part of the margin of the caudal region is due to fossilised muscle. ‘The cranium is well calcified in the usual small tessere, and evidently not much distorted. Its postorbital part is about as broad as long, and the postorbital processes are small and slender. ‘There is very little constriction between the orbits, which are completely. within the hinder half of the cranium. The olfactory capsules form relatively large rounded lateral prominences in the middle of the cranium. The rostral part is short and wide, not tapering but nearly truncated in front, and remarkable for the large size of the elongated anterior fontanelle which extends backwards between the olfactory capsules. There is no indication of a posterior fontanelle in the cranial roof. ‘The jaws are not seen, but there appears to be a vague trace of the mandibular articulation on the right side well behind the occiput. All the vertebre are crushed and broken, but they show much secondary calcification round the primary double-cone, and this seems to have been in concentric lamin (on the tectospondylic plan). As in many other fossil Elasmobranchs from the lithographic stone, the body-muscles are well preserved; and it is clear that while in the abdominal region each myotome corresponds with one vertebral centrum, in the anterior part of the caudal region each myotome comprises two 234 DR. A. SMITH WOODWARD ON vertebral centra. There is thus the common diplospondyly. The vertebral arches are scarcely seen, except within the caudal fin, which is displayed in direct side-view. Here the hemals are apparently stouter and Jess inclined backwards than the neurals. The pectoral arch is only imperfectly shown, but the right pectoral fin is complete. It is relatively large, and the supporting cartilages extend only about half-way from its insertion towards the distal margin. The three basals ave distinct, the propterygium being comparatively small and narrow, the triangular meso- pterygium about as wide as long, and the metapterygium longer than wide but very little produced backwards. The radial cartilages, which are not much longer than the basals, are rather sparsely arranged and do not clearly exhibit any transverse articulations, About 12 are arranged along both the mesoptery- gium and the metapterygium. Faint striations are seen in part of the fin-membrane, but there are no distinct remains of dermal rays. The pectoral fins extend as far backwards as the pelvic fins, which ave much smaller. The pelvic basipterygium is long and gradually tapering, and bears at least 17 radial cartilages, which (like those of the pectoral) are not closely pressed together and do not show any transverse articulations. ‘The cartilages occupy only half of the total expanse of the fin. As they are imperfect behind, the sex of the individual is uncertain. Of the median fins, one large dorsal, bordered in front by the remains of a smooth, laterally compressed spine (d’), arises just behind the origin of the pelvic fins; but it is very imperfectly preserved. The impression of the fin-membrane shows some fine striations, which may perhaps denote strengthening dermal rays. As the tail of the fish is relatively long, this is doubtless the first dorsal fin, but the fossil is too fragmentary to exhibit the second dorsal. The caudal fin, which is displayed in direct side-view and only incomplete at the upper extremity, is long and ovoid, with the lower lobe the larger. The membrane here again shows faintly some fine striation. Just in advance of its lower lobe, a small deep and narrow fin is shown (a.), with most of the outline defined by oxide of manganese. Though its separation from the caudal is a little obscured by the rough fracture of the rock, it is almost certainly distinct and may be regarded as an anal fin. Fine shagréen covers the whole of the trunk and fins. Near the margins it is especially smooth and dense, but on parts of the trunk the granules are rather stellate. On the trunk in front of the pectoral fins, and again on the tail just behind the pelvic fins, it is interesting to notice that the course of the lateral line is marked by a close series of incomplete ringlets (fig. 2a), as in Chimeroids and in the extinct dog-fish, Mesiteva. Young Specimen.—A second specimen inthe British Museum (No. 37014), from the same formation and locality, only 30 em. in. Jength, evidently represents a young individual of the same species. ° The cranium and vertebral column are in undisturbed series, with the two dorsal fin-spines in their natural position on TWO NEW ELASMOBRANCH FISHES. 23) the tail; but the parts of the paired fins are scattered, and only fragments remain. The specimen, however, is of special impor- tance, because displaced portions of both jaws with groups of the teeth are also preserved. The characteristic large anterior fon- tanelle in the cranium is well displayed as in the type specimen, The teeth (fig. 3) are relatively small and closely arranged, several series evidently functional at one time. Their exact shape is difficult to determine, but they seem to be transversely elongated rhomboids, with a low crown, which is smooth, compressed antero- posteriorly to a sharp edge, and sometimes rising in the middle to a little cusp. Many of the vertebral centra clearly exhibit the secondary calcification round the primary double-cone. A frag- ment of a pelvic fin seems to denote a male individual, and a row of slightly enlarged, pointed shagreen-granules may have belonged to the clasper. The two dorsal fin-spines (fig. 3a, d', d’), though fractured, are shown to be nearly similar in size and shape, and their leneth equals about one-quarter of the distance between their insertions. The spine of the first dorsal is supported not only by a short triangular cartilage behind, but also by a larger and more extended cartilage in front. Traces of the fine stellate shagreen are seen on the rostrum. A { finities. —The new genus and species now described evidently represent a family closely related to the Spinacide, but still re- taining the anal fin and a less specialised dentition. Protospinaxr is indeed a generalised type such as might be expected among Juvassic Hlasmobranchs when the Batoids were beginning to be differentiated. The Batoids themselves were first represented by the Rhinobatide. and it is interesting to notice that one member of this family (Belemnobatis) contemporary with Protospinax had a spine in front of each of its two dorsal fins. EXPLANATION OF PLATE I. Fig. 1. Orossorhinus jurassicus, sp.'n.; nearly complete fish, nat. size.—Litho- eraphie Stone; Hichstidt, Bavaria. I, II, IJ. the three paired dermal lappets.. [British Museum no. P. 11211. ] 2. Protospinax annectans, gen. et sp. n.; fragmentary fish, one-sixth nat. size.—Ibid. a. anal fin; d!. spine of first dorsal fin. [British Museum no. P. 8775. ] 2a. Ditto; portion of lateral line of same specimen enlarged four times to show supporting ringlets. 3. Ditto; group of teeth enlarged ten times.—Ibid. [British Museum no. 37014. ] 3a. Ditto; portion of tail of same specimen, showing dorsal fin-spines (d!, d?), nat, size. ON PATHOLOGICAL STATES IN EVOLUTION. 237 14. The Function of Pathological States in Evolution. By Morey Roserts*. [Received May 7, 1918: Read June 11, 1918.] That dissatisfaction with much orthodox biological opinion is growing can hardly be denied. Not a little of this feeling is due to the fact that what is often given as explanation cannot be resolved into factors capable of appreciation, and, possibly, of measurement, by the intellect. The theory has to be accepted as more or less a matter of faith. Where there is a general tendency to rely on authority, speculation is discouraged, for orthodoxy everywhere rests on the native conservatism of man, and even the revolutionary is capable at last of fatigue. As a result, tentative hypotheses offered by the great leaders tend to become objects of faith, and among their less enterprising followers there arises a more or less fervent conviction that, however unsatisfactory they appear now, they will presently become demonstration. Thus the theory of the germ-plasm, even in its later modified form, seems heid too dogmatically by many: the ‘nature’ of inherited living matter accounts for every organ as it appears; while all changes are due to obscure variations of an advantageous kind which give the survivors in the struggle a better chance. On analysis, such opinions do not seem truly scientific, for the “nature” of the germ-plasm can barely be distinguished from the directing entelechy of Driesch, and if the Weismannian cloud of ids and biophors is now somewhat condensed, the magic determinant still remains in a concealed vitalism which is exactly analogous, as regards the organism, with pantheism as regards the universe. Nor, if we are told with certainty that altered characteristics are not trans- mitted, is the theory of small advantageous variations much more satisfactory, if we know neither how they come, nor how they are inherited. To say so much must not be regarded as treating with disrespect its great author, without whom we might still be wandering in the barren field of teleology. To regard these theories as hasty and, perhaps, unsound explanations is not to accept without scrutiny the theory of the transmission of acquired, or modified, characteristics. Though this is a view that can be defended on the physico- chemical grounds of catalysts which are measurable determinants of a really scientific order, experiments to prove the fact must take a very long time, and we are compelled to rely on other methods of proof. ‘That the experiments of Tower and Kam- merer, for Instance, suggest the transmission of modifications cannot be denied. Such as oppose the general view that the environment has thus an inheritable moulding influence on the organism, seem to reply that these are only rare and doubtful * Communicated by the SECRETARY. 238 MR. MORLEY ROBERTS ON THE FUNCTION OF eases, whereas the theory of inherited advantageous variations, whether continuous or discontinuous, can be made responsible for the whole of the phenomena. As the conclusion is gradually being strengthened that large variations of a Mendelian character deal with other characteristics than those which are racial, all who rely on inherited spontaneous variations are forced back on the Darwinian view that small variations can gradually, if of an advantageous kind, convert one species into two or more, and that all living characteristics, or organs themselves, are due to such a cumulative effect. It is, of course, inferred and definitely stated by Darwin, that any variation in the least degree injurious would inevitably be destroyed. It is this statement I propose to examine, and for the purpose of such an enquiry it must be clearly understood what is meant by the word ‘disadvantageous’ or injurious. At first sight nothing seems clearer. Why should we doubt that any functional or organic failure is a handicap in the biological race? By functional trouble of which the cause is not obvious: we mean some hindrance, which may be recovered from, to normal or physiological action. It is due to factors which, for the most. part, are unknown. We do not doubt that there is a failure somewhere, which, as regards certain cells, might be called organic, but often we cannot do more than guess where the actual failure occurs. In that advanced disorder of function which has visible lesions and destruction or irremediable alteration of the individual parts of the machine there is un- doubted organic disease. Can anything seem more certain than the conclusion that any organism which fails in the established functions of its species is as a fact severely handicapped, that the variation is disadvantageous and cannot possibly be trans- mitted either directly or by survival? There are, however, some reasons for believing that this inference is inaccurate and that the function of disease in evolution is of much greater import- ance than that of mere elimination. But pathology has very naturally been neglected as a study by biologists. On the views generally held, it has seemed sutlicient to recognize that disease destroyed organisms which obviously left offspring, if it left them at all, that were handicapped even more heavily than their parents. It has been understood that their elimination was only a matter of time and that neither their virtues nor their failures could influence the race. If there is one thing more than another which has struck me when attempting to study these questions, it is that too many men of science appear to believe that any serious investigation of other branches than their own is for them a waste of time. The physiologist ignores the pathologist, who in his turn is far too likely to fix his eyes on morbid phenomena which cannot be properly appreciated save by those with a knowledge not only of normal function but of the general physiology which underlies is. The same can be said of most workers in science, but in no PATHOLOGICAL STATES IN EVOLUTION. 239 case is it more likely to occur than in that of the biologist, who, by the very name and nature of his task, should include in his apparatus a considerable knowledge of everything which deals with the organic, and even inorganic, world. Science, however, is kept in more or less water-tight compartments, and it seems left to the mathematician to hold the opinion that his own branch of learning has, somehow or another, deep relations with all things, including life itself. Even by him it does not seem to have been pointed out that in things living and non-living certain principles of construction rule alike. However much they were wedded to mechanico-physical explanations, biologists have assuredly often ignored the fact that any organism is con- struction, and knowing little of the laws of construction have ignored basal facts familiar to every architect or even every artisan. It was reserved for Wolff, in formulating his law of bone-growth and reaction to stress, to propound a principle more far- reaching than he recognized, ‘when he showed that living bone, reacting to normal or “abnor ‘mal stimulation, can be pr -oved to develop in accordance with the principles of engineering and architecture. This law may, I feel assured, be extended to every living tissue, and in such an extension will be found the key to many phenomena still awaiting explanation. To one who holds this view, the work lately done by Starling on the ‘“ Law of the Heart,” a i Y, = bv] Vi VroreT L at 1 > a8 a. aA ig TY Weis it! 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