iat be ot Sees Oo eaeeaiee : Sreaeeet eee tar ee 7 ‘ ay beigeat PROCKEDINGS OF THE SCIENTIFIC MEETINGS OF THE ZOOLOGICAL SOCIETY OF LONDON FOR THE YEAR PRINTED FOR THE SOCIETY, AND SOLD AT THEIR HOUSE IN HANOVER SQUARE. LONDON : MESSRS. LONGMANS, GREEN, AND CO, PATERNOSTER ROW. i Es ats aes OF THE “COUNCIL AND OFFICERS OF THE ZOOLOGICAL SOCIETY OF LONDON. 1886. COUNCIL. (lected April 29, 1886.) Prorgessorn W. H. Frowrr, LL.D., F.R.S., President. Liror.-Gen, Tae Lorp ABIncer, Cap} Wittram T. Branrorp, Esq., F.R.S. Masor-Gun. Henry Crerx, R.A., F.R.S. Henry E. Dresser, Esq. Cuartes Drummonp, Esq., T'rea- sure’. F. DuCanr Gopmay, Esq. Lievr.-Cot. H. H. Gopwry-Atvs- TEN, F.R.S., Vice-President. Artnur Grote, Ese., Vice-Presi- dent. JD reg ANE Cw ise Ce F.R.S., GUNTHER, Dr. Eywarp Hamirron. E. W. H. Hotpsworrn, Esq. Pxorussor Mrvarz, F.R.S., Vice- President. Prorrssor H. N. Mosetey, M.A., F.R.S. Hewry Pottocr, Esq. Tur Lorp Artuyr Russet. Osprrt Satyin, Esq., F.BS., Vice-President. W. Aysurorp Sanrorp, Esq. Howarp Saunpers, Hsq., F.L.S. Purp Luriny Scrater, Esq., M.A.,Ph.D., F.R.S., Secretary. Sureron-Gen. L. C. Srewarr. PRINCIPAL OFFICERS. P. L. Scrarer, Esq., M.A., Ph.D., F.R.S., Secretary. Franx E. Bepparp, Esq., M.A., Prosector. Mr. A. D. Barrrurr, Superintendent of the Gardens. Mr. F. H. Waternovuse, Librarian. _Mr. Joun Barrow, Accountant. Mr. W. J. Witxiams, Chief Clerk. LIST CON TE inB UG OURS, With References to the several Articles contributed by euch. g : ANbeRSON, R. J., M.D., ‘M A., Professor of Natural History, Queen’s College, Galway. On the so-called Pelvisternum of certain Vertebrates... .. 163 Bepparp, Frank E., M.A., F.R.S.E., F.ZS., Prosector to the Society. Preliminary Notice of the Isopoda collected during the Voyage of H.M.S. ‘ Challenger.’ —Part III. ............ 97 Note on the Air-sacs of the Cassowary.... .. 145 On the Syrinx and othcr Points in the Anatomy of the Caprimulgidze 147 Note on the Structure of a large Species of Earthworm from New Caledonia. (Plate XIX.) .......... 168 On some Points in the Anatomy of Ohauna chavaria.... 178 Observations on the Ovarian Ovum of Lepidosiren ( Pro- topterus). (Plates XXVIII. & XXIX.Y. 22.0.0... 272 Descriptions of some new or little-known Earthworms, together with an Account of the Variations in Structure exhibited by Perionyx excavatus, E. P. .............40- 298 Notes on the Convoluted Trachea of a Curassow (Notho- crax urumutum), aud on the Syrinx in certain Storks...... 321 Observations on the Development and Structure of the Ovum in the Dipnoi. , (Plates LII.—LIV.) .. .... ececli on. BOR lv Page Bewt, F. Jerrrey, M.A., Sec. R.MS., F.Z.S., Professor of Comparative Anatomy in King’s College, London. Remarks upon the Species of Balanoglossus exhibited to the Society on November 17th last year ...........-++-- 154 Note on Bipalium kewense, and the Generic Characters of Land-Planarians; (Plate XVIIL.) ...0.....0--00sen0e ae Exhibition of, and remarks upon, an object made from some portion of the skin of a Mammal ...... .... 0... - se eees 420 Exhibition of, and remarks upon, a specimen of Tenia nana 503 Buanrorp, Witit1iam Tuomas, F.R.S., F.Z.S., &c. Exhibition of, and remarks upon, a stuffed skin of Para- COXUFUS J TAONA. 5 5 yao do G2 -0u oes «son 6 Dale eckoselays og Be AMctete wae Boutencer, G. A., F.Z.S. Description of a new Iguanoid Lizard living in the Society’s Gardens: (Plate KAIIL.) ... 25 pewipeieees Pee ee 241 Remarks on Specimens of Rana arvalis exhibited in the Society’s Menagerie. (Plate XXIV.) ........02 + eeeeee 242 First Report on Additions to the Batrachian Collection in the Natural History Museum. (Plate XXXIX.) ........ 411 On two European Species of Bombinator. (Plate L.).... 499 On the South-African Tortoises allied to Testudo geome- drica. 4 (Plates LVL Lee L VINE.) 0... cite s.c ee eee 540 Remarks on Prof. W. K. Parker’s paper on the Skull of the Chameleons........... ia a's Seals Pea ote oa en Bourne, Atrrep Grsps, D.Sc. (Lond.), F.L.S., Fell. Univ. Coll. Lond., Fell. Madras Univ., Professor of Biology in the Presidency College, Madras. On Indian Earthworms.—Part I. Preliminary Notice of Earthworms from the Nilgiris and Shevaroys............ 662 Bourne, Giusert C., B.A., New College, Oxford. General Observations on the Fauna of Diego Garcia, GRaSee MTOM: .\.ereta news 3 tit stele ee ee bette eke eee 331 ¥ Page Brapy, Georcr Stewarpson, M.D., F.R.S., F.L.S., Professor of Natural History in the Durham College of Science, Newcastle-upon-Tyne. Notes on Freshwater Entomostraca from South Australia. Pete AN EE Ria Wate, Be in AS sg he a brakta Coates Sea pyre 82 Butter, Artuur G., F.L.S., F.Z.S., &e. DRO He GN APOE METAR: oan ic nse wns g she banter cas see y's ER 80 On Lepidoptera collected by Major Yerbury in Western Poe GCP RON YM waiciare « pias «Weer O95 CocKkERELL, T. D. Exhibition of, and remarks upon, a living specimen of a Variety of Parmacella valenciennesi...........00.+0++++ 137 Couett, Rosert, C.M.Z.S. Notice of a Memoir containing an Account of the External Characters of the Northern Fin-whale...............00 82 On a new Pediculate Fish from the Sea off Madeira. PLO ORV) 4 aya areca eet ade is Seater xia crate eaiaes, LOS On the Hybrid between Zagopus albus and Tetrao tetriz. (Plates XXI. & XXII.) . es ee 2 On the External Characters of of Rudolph? S Donan (Bale- noptera borealis). (Plates XXV. & XXVI.)............ 243 On Phascologale virginia, a rare Pouched Mouse from Northern Queensland. (Plate LX.) ............-+ alvaepoae Corné ty, J. M., C.M.ZS. Letter from, respecting the breeding of Michie’s Deer in PAN GMEHARONEG, “Sn spatels's 0 gas sot we're toe sews pero Cenieerd | OLO Crane, AGNES. On a Brachiopod of the Genus Atretia, named in MS. by Palate Del: Davidedis, oc). 2s iazeniosgs .cekeesnsa- 18h e Page Crow ey, Puiip, F.Z.S. Exhibition of some Pupz of Nocturnal Lepidoptera from Watale ce. oe ci occas daak. cic 0 Uh eee ea eee Cunnincuam, J. T., B.A., F.R.S.E., Fellow of University College, Oxford, and Superintendent of the Scottish Marine Station. On the Mode of Attachment of the Ovum of Osmerus eaerigma.. (Plite: SEM) ions sb a's ape- was ons min Se Dosis, W. H. Exhibition of, and remarks upon, a specimen of Sabine’s Gull (Yema sabinii), shot at Mostyn, on the coast of Flint- shires NOLEDAW ALES fispc orstyeya sie’ o oh oreysima eee Dic ASE oe ee Druce, Hersert, F.L.S., F.R.GS., F.Z.S. Descriptions of some new Species of Heterocera from Tropical Africa. (Plates XXXVITI. & XXXVIII.)........ 409 Exwes, Henry Joun, F.Z:S. On Butterflies of the Genus Parnassius. (Plates 1.-IV.). 6 Emin-Bey, Dr. Letter from, containing remarks upon the presence of an Anthropoid Ape in Eastern Equatorial Africa............ 418 Finsca, Dr. Orro, C.M.Z.S. &e. On a new Species of Wild Pig from New Guinea... .... 217 Fiower, Witt1am Henry, LL.D., F.R.S., F.L.S., President of the Society, Superintendent of the Natural History Collection, British Museum. Exhibition of, and remarks upon, a rare species of Armadillo belonging to the Museum of the Scarborough Philosophical I a ain ae Oe cee te ae cee a eo Gerrarp, Epwarp, Jun. Exhibition of specimens of the heads and skulls of two African Rhinoceroses (Rhinoceros bicornis and R. simus) .. 125 vii Gopman, Freverick DuCang, F.R.S., F.LS., F.Z.S. Exhibition of a series of examples of Danais plexippus from various localities .... Gooncuixp, J. G., F.Z.S., F.G.S., H.M. Geological Survey. Observations on the Disposition of the Cubital Coverts in 154 TLE ee ae Penn See» ee ae I ge 184 Goruaw, Rev. H. S., F.Z.S., F.E.S. On new Genera and Species of Endomychide. (Plate “a er ee Me eee ene eee Oe ere 154 GintHerR, Atsert C.L.G., M.A., M.D., Ph.D., F.R.S., F.Z.S., Keeper of the Zoological Department, British Museum. Second Note on tle Melanotic Variety of the South- IRE WCU DRE: . or.5367, Stniees See vic sihe is Sunil Ghee Siete < SENS 203 Exhibition of a specimen of a small Fish of the genus Fierasfer imbedded in a Pearl-Oyster ...............455 318 Kirpy, W. F., Assistant in Zoological Department, Brirish Museum (S. Kensington). Remarks on four rare Species of Moths of tze Family ppeegier) SCL ate Oe WELL ee Sos ed. SS ee ee 269 Cn asmall Collection cf Dragonilies from Murree and Campbellpore (N.W. India), received from was J. WW. Merbury, i. AS “(Plate Deer ye ae ales Oa. 325 Lankester, E. Ray, M.A., LL.D., F.R.S., Jodreli Professor of Zoology in University Coiiege, London. Exhibition of a drawing of a restoration of Archaeopteryx. 125 Layarp, EpGar Leropotp, F.Z.S., H.B.M. Consul, New Caledonia. Exhibition of a rare Beetle, and of a series of Shells of the genus Bulimus . 267 Vill Page Lrecu, Joun Henry, F.L.S., F.Z.S. On a Variety of Anthocharis eupheno, from Mogador.... 122 LEeNDENFELD, R. v., Ph.D., F.L.S., Assistant in the Biological Laboratory of University College, London. On the Systematic Position and Classification of Sponges. 558 LurKen, Dr. Curistian F., F.M.Z.S. &e. Letter from, containing a notice of the habitat of Chiropo- dona: penicilattis accom 2a 56 cb been ss «ne 2c ns eee LypEkkeER, R., B.A., F.G.S., F.Z.S., &e. Description of three Species of Scelidotherium. (Plates REVI. RETR eee caves or ee Seen Toe ace tee Martn, J. B., F.Z.S. Exhibition of a large Tusk of the Indian Elephant ...... 176 Maruew, Gervase F., Staff-Paymaster Royal Navy, F.L.S., F.Z.S., &e. Descriptions of some new Species of Rhopalocera from the Solomon Islands. (Plate XXXIV.)............42 -+ +02. B43 Meyer, Dr. Apotr Bernuarp, C.M.Z.S., Director Royal Zoological Museum of Dresden. On a fourth Male Specimen of King William the Third’s Paradise birds. on oo.ck Peale 2 pe. dene <3 2.9.25 ab ae ee Letter from, communicating remarks by Mr. K. G. Henke on a specimen of Hybrid Grouse in the Dresden Museum .. 419 Mituais, Joun G., F.Z.S. Exhibition of, and remarks upon, specimens of the Ivory Gull (Larus eburneus), shot in Scotland ........++...+-- 137 Minot Dr. C.S. Letter from, calling attention to the Elizabeth Thompson Science UNE ceca cc ac 6 GN @ eicfoulsiandie cls o's aie eee hels beeatet: 6 Page Monticetty, Fr. S., D.Sc. Contribution to a Knowledge of the South-Italian Chiro- RCCL A areey fetter tpaNete tale octave atta Mammon oct chet weete" iol al obs ocd 93 Ocixsy, J. Doucias, Department of Fishes, Australian Mu- seum, Sydney. On an undescribed Pimelepterus from Port Jackson .... 539 Ramsay, R. G. Warpuaw, F.Z.S., F.L.S. On a new Species of Bird of the Genus Copsychus ...... 123 Rosset, C. W. Exhibition of Photographs taken in the Maldive Islands, and remarks on his Zoological Collections ........... omen 290 Satvin, Ossert, F.R.S., F.Z.S., &e. Exhibition of, and remarks upon, a living specimen of Bipalium kewense, found at Hawksfold, Sussex .......... 205 Saunpers, Howarp, F.L.S., F.Z.S., &e. Exhibition of, and remarks upon, an adult specimen of the Sooty Tern (Sterna fuliginosa) caught near Bath ........ 6 On the Birds obtained by Mr. G. C. Bourne on the Island ei@hers Garcia, Chases Growpit iis) «6 <6 «leied oes wos 3% 25885 Exhibition of, on behalf of Mr. R. J. Howard, and re- marks upon, a specimen of a hybrid between the Tufted Weakened PNeNROCHATA ts ac co 8s set athe tan aiae's oe olan 550 Sciater, Paiwie Lutwey, M.A., Ph.D., F.R.S., Secretary to the Society. Report on the additions to the Society’s Menagerie in BCE HEED OG De! on .\c (cf Pah mc kl) ap opine aegesineea te al Exhibition of Lepidopterous Insects bred in the Insect- house durmig the part SeasAN .<<6+.e a Il. ( Structure and Development of Parnassius .......... 6 IV. ‘ MMe ES IS woe Seo BO SE ADO Orolo cae SCO ae 54 WA se SCIRTOPLETUS CRUSOE 6 oa a.6s vse alee see owes fomeee so VT ee) file, MOWeST rast Sete Cie ha reae afofele) siejntatolehensy aielielde ac pe 79 VDI IX. | New Australian Entomostraca ....,.00eseeeeereces 82 X. XI. Skulls of Mustela pennanti oo... eevee tcveee neni 125 XII. xin. Stephanotrochus moseleyanus .,....++..>+ 128 XIV. MV mme LEO IIE TLUCH CR: ale « -fayategtiierotatolel ae este) « 0 s1s eho «= 138 XVI. Fig. 1. Head of Rhinoceros simus. Fig. 2. R. bicornis. 143 XVII. New Coleoptera of the Family Endomychide ........ 154 XVIII. Bipalium kewense, in various stages of contraction . 166 RIX. Acanthodrilus layardi.. 000 sve ccseaens . 168 KX. Hyhodus dubrisiensis, Mackie... 2... 0006 20000. .se0ee 218 heen Hybrid Grouse between Lagopus albus and Tetrao tetriz. 224 PONCE NGFenosawr a CryeenOnuel aS 0 sleinye,si(s\ cists) els alels| oe) ole) eel ne «yo = 241 SONG STOUT ier’ os eta ond an tae ne babe oC aa oouoe mar 242 XXV. : F XXVL OLERODLEN GA OGTEMUSI oars iateleleree ollcielehstaicls vel» © = eve 243 XXVII. New or rare Sphingide............. Sonioncentpacen 269 XXVIII. f Pr 979 XXIX. Ovyarols Proto ptertisitey.c at -\eter nice vere xts)e\ vsleelel a eltelsvellete = 72 XXX. Ovum of Osmerus.......... 292 ert PERETTI SNE cco: ated. acca ME RE 314 XXXII.) Capra sinaitica, 3 a XXXIII. Dragonflies from N.W. India...... 0... eee c eee eee -. 325 XXXIV. New Butterflies from the Solomon Islands .......... 343 XXXV. New Lepidoptera from Western India.............. 355 Xvi Plate Page EONONGVI SPL OCNICOMLETUS AMES fore = =o < vious ce oils sisal eee 395 CLOG = al GTC PO" Ser Ce DMIB eID CAO PO ARO ROC Ae coe 409 XXXVIII 1. Bunea pygela. 2. Antherea dolabella ae 409 3. Chrysopoloma rosea. 4. Chrysopoloma citrina.. XXXIX. 1. Ivalus asper. 2. Geomolge fischeri .............. 411 Sr New Indian Lepidoptera®?: cae arta ac sneer 42] XLII see: Anatomy of Geococcyzx californianus........+. +++. 466 XLV. XLVI. Scelidotherium leptocephalum............+.+++++. ) XEVIE Scelidothertumbravardt.. 2. ...2....00ccscas os | XUEVUL Seelidothermmchtlense. . scree’. + «2 oe ace eine totes » 4%) XLIX. Fig. 1. Scelidotherium bravardi. Fig. 2. S. chilense. | Fig. 3. S. leptocephalum. Fig. 4. ?'S. bravardi.. | L. Fig. 1. Bombinator bombinus. Fig. 2. B.igneus .. 499 Wile siGacellamasOnncs Ao oh get See ee noe ee 504 LII. LIII. + Structure of Ovum in the Dipnoi ..........-....... 505 LIV. UaV.c1Squaloraydon<). Rast eee cele neers stone oat 527 ANE Conus UTIL OT GUIS toe ele lanoleielalelefeeeio ite tera 538 VES 05 Lesindo vtvaments.;< 2220s ws Seen ce tte stains | 540 DL VEDE » Wes ittedos Gish. sain. wien ogee bien eee Ge { LIX. Figs. 1-7. Lagostrophus fasciatus. Figs. 8-12. Lagor- EhestEes bepOrOrdes ar oro «|= lavoro nate lee aiokes helo elo eee 544 EX? “Phascologale cig vince crore ernie sees ine ee 548 LIST OF WOODCUTS. 1886. Page Co eS REE MELE PST A nS a SAHOO Sele Estheria lutraria ...... + (EROS iNOS DER ORCOG OoOINe Foc Ola hit Oimesk es PR MEIA POLK UES TP Sei es Scag a tess sce ea tise yee: Sic OTE Whe tele, PR MUARGGUE TEDOEMGE OS. 1. Le teeta ae vs See oases SF OMEN Bitideat ese PIADNSIN OMCUILUDE Ea aia sivle olive ic lttce Dees Va teehee NSS ory teks. Diagrams of the arrangement of the septa in the five different species OLUSCMNUNUOCIUBSO Sa ialtstconia Sar oe cee cae ee ke det God: Syrinx of Nyctidromus albicollis ..... ccc. cece ue eenees Shiva 49 Syrinx of Afyotheles nove-hollandi@ ...........45 PS eetts .. 149 Pyne Or Harrachomanuis Ope ee Ye ales averitettestarromeLOO Cen Of Charen chem 1.55 wine fc aba scis's ess eek eed eae e's 180 UCnubital Region in the’Golden Plover ........6.5 Ze sccceeesvees 186 Cubital coverts in Turdus merula, Corvus, and Alauda arvensis ..., 187 Cubital coverts in Hirundo, Cypselus, Trochilus, Chasmorhynchus, Disc el ora Udo eMepNGsloa” ear tatinsts ile <\cistelets aleiststolersserite s Mee he 188 Cubital coverts in Psittacus, Melopsittacus, and Calopsitta ........ 189 Cubital coverts in Falco and Phalacrocorar.......cececccvccucee 190 Cubital coverts in Wycticorax, Querquedula, and Meleagris ........ 191 Cubital coverts in Crax, Talegalla, Columba, and Goura ..,....... 192 Cubital coverts in Tetrao, Luplocamus, and Columba ........eeeees 194 simbiial coverts in, Peerocles. (0 him ajereiaisn: mele eniete sa. « Papcieinat es can: 195 Cubital coverts in Carpococcyx, Cuculus, and Coccystes ............ 196 FoTiDital COVES Mi, CHhOMmMim te chnes cence ce cele cota.e os i tele ets es 197 Cubital coverts in Gallinago, Scolopax, Rallus, and Sterna ........ 198 Cubital coverts in Alea, Diomedea, Sula, Fregata, and Plotus ...... 199 Cubital coverts in Disswa, Mycteria, and Leptoptilus ......0..0ee 200 (nbital coverts in WSarcorvRapnus. .. ccc ss ccecrccase sere ervey ». 201 Cubital coverts in Grus, Gypogeranus, and Pandion...........0005 202 Flat skin of Felis leopardus, var. melanoticd.......0.c ee caeee scans 204 The right funicular pouch of peritoneum of Macacus sinicus ....,, 208 Perforating ulcers in an early stage affecting the feet of a Paradoxure, INET NUD GET ETT re ROPER OOO EI PEI OIC OIEOXCICIONS DIO.) Oyo Danycir 209 Examples of symmetrical exostoses in the skeleton of a Monkey..., 210 A Cockateel, Calopsitta nove-hollandie, with symmetrical sebaceous CATS OM TCRE WALES Us lar cnecareilahets iulg rid oo atelacg OTRanmei yl uiearatone, ehstetn| b's 211 A follicular cyst from a Prehensile-tail Porcupine, Sphingurus FERLCET OLE Bie 5 le eo OOD IO GONE | toi Ce GTO. aoa eO Doak 212 XVii Page The tunica vaginalis and testis of a Lamb affected with a con- genital parenchymatous hydrocele ........e:eee sees rere eeaee 213 The occiput of an Ichneumon, with dislocation of the atlas and subsequent ankylosis of that bone to the occiput ............ 214 The marsupium of a Short-headed Phalanger, Belideus breviceps, opened in order to show a scirrhous cancer growing from the mammary gland ......sceseeereceeeteeceeteecereeneenees 216 Tleo-czecal intussusception in a Lemur .......-..eee cece eee eee 217 Balenopterus unisetus .. 0... ccccccecceeeeeceennecneeneceeenes OE Echinorhynchus ruber... 00sec cece eee net ence eee e ee ee eens 258 Calanus firmarchicus 0.0.0 cece crete cern eee eee neneeesceee 202 Generative organs Of Fudrilus .......ccccce sense eee e een nc tenes 803 Generative organs of Eudrilus, with bursa copulatrix laid open ..,. 805 Varieties of Pertony® eXCQVAtUS... 2.6.1 cree neste renee asnencces 310 A small Fish of the genus Fierasfer imbedded in a Pearl-Oyster...,. 319 Trachea of Nothocrax urumutum, SG ces cccccccecccecessccsssesss OE Syrinx of Abdimia sphenorhyncha.... cc. cccevee ec eeneeeeenneeas 323 Syrinx of Xenorhynchus senegalensts... 0.60.6 c cre ee reeves neeenes B24 A vertical section through the body of the axis to show the lenticular- shaped piece of cartilage in Man .........seseeececeeeceeee 338 A diagram of the axis vertebra to show the various nuclei in Man.. 339 A section through the human sacrum, showing the epiphysial plates uniting with each other peripherally before fusing with their CONLTA tania meses Meee eee cit eis Grie iaiistess Biersl> oeanee 340 Axis vertebra of a young Seal in section, showing the epiphysial plates of the true centrum of the axis .......... Soncesoueon: 341 Map of the vicinity of Tarapaca, Chili.......-..... sess eeeeneeee 396 Bill of Pheenicopterus ANdinus oo 2csreveevevesecrsccsecascesees 400 Bill of Phoentcoptercs. JAMest .. 0%. cece ccawet essere csrsesssrecns 400 Right columella of Ichthyosaurus ...0. cee ce eee cece neenenneens 407 Lower portion of right columella of eee sg psobsoo nace 407 Lower portion of left columella of Ichthyosaurus intermedius ...... 407 Waeft columella of Hatierzn gincbata ea. 6010 20 vin duun aici) als 2m) siotooe 407 Muscles at the outer side of the elbow of the right wing of Caprimuligus CUnOp@Us oe e oisc05 6 a 0in ajsinin e's 8s av enone omen ea 471 Muscles at the outer side of the elbow of the ieft wing of Steatornis. 471 Anconal aspect of the left humerus of Tachycineta thalassina ...... 502 Palmar aspect of the left humerus of Tachycineta thalassina ...... 502 Anconal aspect of the left humerus of Micropus melanoleucus ...... 502 Palmar aspect of the left humerus of Micropus melanoleucus ...... 502 Anconal aspect of the left humerus of Trochilus alexandri ........ 502 Palmar aspect of the left humerus of Trochilus alevandri ......++4. 502 ERRATA, Page 164, 5th line from top, for “ Subilium” read ‘ Suprabilium,” and for ” “ Subscapula ” read “ Suprascapula.” 164, 14th line from top, for ‘‘ Preomosterna” read “ Preomosternum.” 164, 15th line from top, for ‘‘ Hemi-pelvisterna” read “‘ Hemi-prepelvi- sterna.” 164, 16th line from top, for ‘‘ Substernal” read “ Suprasternal.” 257. For Balenopterus read Balenophilus. 262. After Calanus finmarchicus, add “length 2 millim.” 265. Last line for “ enlarged” read “ diminished.” 28. 19th line froin the bottom for “ N.-American” read “ N,-Indian.” Myel the samy webs: A, Ay Say } (Mia ip Bt Ye aa} *bensan WAL SA that A — 2 F s A Friall>, JO Wh Sted ei) oboe aendt iettly FG i. mall r PROCEEDINGS OF THE SCIENTIFIC MEETINGS OF THE ZOOLOGICAL SO Y OF LONDON. a Sy. January 19, 1836. Prof. W. H. Flower, LL.D., F.R.S., President, in the Chair. The Secretary read the following report on the additions to the Society’s Menagerie during the month of December 1885 :— The total number of registered additions to the Society’s Mena- erie during the month cf December was 157. Of these 2 were by birth, 137 by presentation, 2 by purchase, 2 by exchange, and 14 on deposit. The total number of departures during the same period, by death and removals, was 116. The most noticeable additions during the month were :— 1. A male Cheetah (Cynelurus jubatus), received December 8th, presented to the Society by Nawab Mirza Hassim Ali Khan, of the Afghan Frontier Survey. A pair of feline avimals captured, in November 1884, near the Istoi Pass on the Perso-Afghan frontier, when quite young, after the mother had been shot, by some of the members of the Afghan Boundary Commission, were believed at the time to be Snow-Leopards (Felis uncia)', and were forwarded to Pisheen, where they were kindly kept through last summer by Mr. H. J. Barnes, Political Agent at Quetta. The survivor of them, having arrived in this country, proves to be not a Snow-Leopard, but a fine young male Cheetah (Cynclurus jubatus). The Cheetah was well known to occur in Persia (see Blanford’s ‘Kastern Persia,’ vol. ii. p. 35), but I am not aware that its occurrence so near the frontiers of Afghanistan has been actually recorded. 2. A young female Tiger, deposited by J. E. T. Aitchison, Esq., 1 See Sir Peter Lumsden’s letter, P. Z.8. 1885, p. GLO. Proc. Zoo, Soc.—1886, No. I. ] 2 MR. A. THOMSON’S REPORT ON THE INSECT-HOUSE. [Jan. 19, M.D., Naturalist to the Afghan Boundary Commission, This specimen seems to belong to the small and densely furred form of Felis tigris prevalent in northern latitudes. This animal is stated to have been captured on the Hari-rud, between Sarakhs and Pul-i- Katim. 3. Four young Gazelles obtained during the survey of the boundary of Northern Afghanistan, and deposited by the same gentleman. These Gazelles are probably referable to Gazel/a sub- gutturosa, but seem to differ somewhat from our previously received specimens of the same species. 4. Two curious hybrid Ducks bred in 1884, at Cannes, between the Ruddy Sheldrake (Tadorna rutila) and the Egyptian Goose (Chenalopex egyptiaca). This pair of hybrids was presented to Dr. T. E. Charles, of Cannes, by Madame de la Blanchetain, of the same place. Dr. Charles presented them to Sir Joseph Fayrer, who has kindly transferred them to the Society’s Collection. The Secretary laid upon the table a series of specimens of Lepidopterous insects which had been bred in the Insect-House during the past season, and read the following report upon the subject drawn up by Mr. A. Thomson :— The following species of insects have been exhibited in the Insect-House during the past season :— Silk-producing Bombyces. Indian. Attacus atlas. Attacus pernyt. cynthia. Actias selene. ricini. Antherea mylitta. American. Samia cecropia. Actias luna. i ceanothi. Hypochera io. Telea polyphemus. African. *Gynanisa maia. * Bunea caffraria. * Anthereea cytherea. * Cirina forda. sf tyrrhea. Diurnal Lepidoptera. Papilio podalirius. alexanor. machaon. asterias. Thais polyxena. Parnassius apollo. Aporia hippia. crategi. * Exhibited for the first time. Huchloe cardamines. Lycena corydon. *Timenttis disippus. Vanessa antiopa. atalanta. levana. , Var. prorsa, Melitcea cinvia, 1886.] MR. A. THOMSON’S REPORT ON THE INSECT-HOUSE. 3 Nocturni. Smerinthus ocellatus. Bombyx quercus. popult. * Hemileuca maia. tilie. Lasiocampa quercifolia. Sphinx ligustri. * Dipthera ludifica. Deilephila euphorbic. Endromis versicolor. * Hemaris marginalis. Saturnia carpini. Euchelia jacobee. Dicranura vinula, Callimorpha hera. *Clostera anachoreta. Aretia caja. Notodonta ziczac. Chelonia villica. Catocala fraxini. Liparis chrysorrhea. It will be noticed from the preceding list, that the three species of European Papilio, viz. :—P. podalirius, P. alewanor, and P. machaon, have been exhibited, and that specimens of Pupilio asterias, from N. America, were exhibited for the. first time. Together with the pupee of this last-named species, I obtained some very small larve (hybernating) of Limenitis disippus. They had spun up in small leaves, but after being in the warm Insect-House for a few days, they came out and commenced to feed very freely upon weeping willow ; they grew rapidly and ultimately produced some very fine imagos, some of which I have the honour to exhibit this evening. I again obtained by exchange some larvee of Aporia hippia, and I took the opportunity to get a coloured drawing made of the larve, pupa, and imago of this little-known insect, which I now exhibit’. Of the American silk-producing Bombyces, Samia ceanothi was exhibited for the first time, and I succeeded in obtaining fertile ova from one pairing, and in due course the larve ; but I regret to say that they all died. Of the 2nd, 3rd, 4th, and 5th stages, I exhibit coloured drawings which Mr. F. W. Frohawk was good enough to make from the living larve. The larve in the first stage were black, similar to those of Samiu cecropia. Although the pure-bred larve died, some hybrids which I obtained from a pairing of a male Samia cecropia with a female S. ceanothi, throve remarkably well, and there are over 60 cocoons now in the Insect-House, from which the insects may be expected to emerge early in the coming spring. Early in the past season, I purchased about four dozen large pupz from South Africa, which had been stripped of whatever cocoon or other covering they had possessed, so that it was not possible to determine to what species they belonged; it could only be seen that they were Bombyces of some kind. As will be seen by the list, examples of five species were obtained from them. They were very irregular in their appearance, the first emerging on May 7th, and the last on September 29th. I obtained a pairing of Gynanisa maia, but the larvee, I am sorry to say, died, although one fed, till it reached its third stage, on Laburnum. Good specimens of Antherea tyrrhea, Fabr., ave, I believe, rather scarce in collections. * See Mr. Butler's paper, iv/fra, p. 80. l * 4 REV. T. R. R. STEBBING ON CRUSTACEANS FROM [Jan. 19, Young larvee were obtained of the following species:—Atétacus atlas, A. mylitta, A. pernyi, and some hybrids said to be hybrids between Attacus pernyi and A. mylitta, and between A. perny? and A, roylei, Actias selene, Samia ceanothi, aud hybrid Samia cecropia and S, cea- nothi. Of these, Attacus pernyi and the hybrids only were reared, the other specimens all died. Every attention was given to them, and I regret to have to express my opinion that the present Insect-House is not a suitable building for rearing young larvee. At the same time, it must be borne in mind that the past season was, in consequence of the long drought, bad for rearing larve, as the leaves of the food- plants became hard and dry early in the summer. Apart from this, the leaves of all trees growing in or near the Gardens get very dirty with smoke, and although the precaution is always taken to wash the food before using it, the leaves are not so fresh and good for feeding as those obtained from the open country. The larve of dttacus pernyi were reared upon the English Oak when the leaves were young and succulent, and they grew very rapidly and did well. The so-called hybrids of Attacus pernyi and Attacus roylei were reared, and a good number of cocoons obtained. The hybrids (?) of Attacus pernyi and Aldacus mylitta did not do so well, and only three cocoons were obtained. One insect from each of these cocoons has emerged up to the present, and these are, in my opinion, dftacus pernyi pure. I tried to obtain pairings of A. pernyi with females of A. mylitta, but did not succeed, although the insects were in the finest condition, and the males of A. pernyi were most energetic in their endeavours to pair with the females of A. mylitta. I had no opportunity of trying this experiment with Attacus roylei, as I had not any of that species. I am sorry to have to record the death, in November, of the very fine Mygale fasciata, which was presented to the Society by Mr. H. R. P. Carter, in January 1885, and of which a life-sized figure was published in the ‘ Field’ of April 25, 1885, together with some notes by Mr. W. B. Tegetmeier, F.Z.S. The colours of this Spider during life were very beautiful. A communication was read from the Rev. T. R. R. Stebbing, containing descriptions of some new Amphipodous Crustaceans from Singapore and New Zealand. The species were shortly described as follows :— 1. ByBLIS KALLARTHRUS, Sp. nov. This new Amphipod was brought from Singapore by Brigade- Surgeon 8. Archer. The most striking peculiarities are the doubly sinuate lower margins of the fourth pair of side-plates, the branchie carrying on their surfaces rows of overlapping secondary vesicles, and the third uropods, in which the inner margin of the outer branch and the outer margin of the inner branch are much ornamented. The head - 1886. } SINGAPORE AND NEW ZEALAND. a in this species is long, very much narrowed distally ; the telson is divided beyond the centre. The following accounts of Talorchestia tumida and Amphithopsis cerulea, from New Zealand, were sent along with the specimens by Mr. G. M. Thomson, their discoverer. His remark that in Amphithopsis (Pherusa?) cerulea the 4th coxa is broader than the preceding three together, applies to the appearance in the undis- sected specimen, not to the coxee or side-plates when drawn apart. “©2, TALORCHESTIA TUMIDA, 0. Sp. General form of body, when seen from above, much inflated. Eyes large (in living specimen of a turquoise-blue colour). Anterior antenne very short, reaching a little past the extremity of the penultimate joint of the peduncle of the posterior pair ; flagellum 7-8-jointed, subequal with peduncle. Posterior antenne as long as cephalon and first two segments of pereion, last joint of peduncle much the longest ; flagellum 12-14-jointed, slightly shorter than peduncle. Males apparently of two forms :— First Form.—First gnathopod with the propodos somewhat curved, its inferior margin distally produced and rounded ; dactylos curved and much longer than the palm ; carpus and propodos with numerous spines. Second gnathopod with the carpus small and triangular ; propodos ovoid and smooth, palm very oblique and furnished with two rows of minute teeth; dactylos two thirds as long as propodos, with its point lying over the edge of the palm. Third pereiopod short, fourth and fifth very long, former with the bases not dilated. Second Form.—Second gnathopod with the propodos broadening towards the distal margin, palm nearly transverse with a blunt tooth between the middle and hinge of the dactylos ; latter furnished with a large tooth impinging outside of the tooth of the palm. Third and fifth pereiopoda normal: fourth with the the carpus nearly quadrate and broadly dilated. Telson nearly as broad as long, quite round at the apex and fringed above with a submarginal row of minute spines. Colour, when alive, ivory-white. Hab. In sandbanks, Purakanui near Dunedin, among roots of littoral plants, many yards from high-water mark. Each specimen inhabiting a hole of its own. When taken out they leap with great vigour. “3, Puerusa (?) CARULEA, n. Sp. Colour of body a deep indigo-blue, appearing black when alive. Length about 5 mm. Superior antenne about 4 mm. long, and considerably longer than the inferior ; last joint of the peduncle with a secondary appendage consisting of a single joint and a terminal seta; flagellum about three times as long as peduncle and very-many- jointed. Inferior antenne about two thirds as long as superior, and with the peduncle reaching slightly beyond the extremity of peduncle 6 _ MR. H.J. ELWES ON THE GENUS PARNASSIUS. [Jan. 19, of the first pair. The mandibles have an appendage. The gnatho- poda are small and subchelate; the dactylos of the second pair is guite peculiar; it does not end in a claw, but in a finger-like setiform process. Pereiopoda very similar in form, the basa being progres- sively dilated ; fourth pair the longest. Telson entire. Coxz of the first four segments very deep, the 4th broader than the preceding three together. Hab. Several specimens of this species were taken in a runnel of water on the Obelisk (or Old Man) Range in the interior of Otago, at a height of about 3000 feet. The stream was a little thing that one could have dammed with the hand, and running at such a slope that I can hardly imagine how the crustacea are not washed away by every shower of rain. The Old Man range is about 80 miles from the sea. The only other fresh-water amphipod found in New Zealand (excluding the subterranean forms found by Chilton) is Calliope fluviatilis, mihi, which is very common.” This paper will be published entire, with illustrations, in the Society’s Transactions. A letter was read from Dr. C. S. Minot, of 25 Mount Vernon Street, Boston, Mass., U.S.A., calling attention to the Elizabeth Thompson Science Fund, for the advancement and prosecution of Scientific Research, and inviting applications for assistance fiom it. Mr. Howard Saunders exhibited an adult specimen of the Sooty Tern (Sterna fuliginosa) sent to him by Mr. A. C. Foot, of Bath, with the statement that the bird was caught alive about three miles from that city, on the 4th or 5th October, 1885, the weather being windy and the floods extending over the meadows. It was brought to Bath on the 6th October, and seen in the flesh by the Rev. Leonard Blomefield and the Librarian of the Bath Museum. Only two examples of this species had as yet occurred in Great Britain. Its habitat was principally intertropical, but it bred as far north as the Florida Cays, and straggled northwards, generally in autumn, to the coasts of New England. Under the name of ‘* Wide- awake Fair”’ its breeding-colony at Ascension was well known. The following papers were read :— 1. On Butterflies of the Genus Parnassius. By H. J. Exwss, F.Z.S. [Received January 19, 1886.] (Plates I-IV.) Notwithstanding that the Butterflies of this genus have for years been especial favourites among entomologists, and that their countless variations have caused many pages of unprofitable descriptions to be written on them, yet our actual knowledge of their life-history is, with 1886.] MR. Hu. J. ELWES GN THE GENUS PARNASSIUS. 7 the exception of two or three species, so slight that it would be quite premature to write a monograph of the genus. But, partly through the numerous scientific explorations which have been carried on in Russian Asia of late years, and partly owing to the high value placed on these Butterflies having encouraged the efforts of profes- sional collectors in remote parts of Turkestan, so large a number of specimens have reached Europe during the last five or six years that a review of the genus is both possible and useful. The principal object, however, in my work has been to investigate the functions and structure of the horny poluch-like appendage which is found in the female sex of the genus, and which seems to have been almost entirely overlooked by most of those who have classified and described the species. I had not appreciated the immense importance of this structure, as a specific and generic character, until I received two years ago, through the kindness of my friend M. Charles Oberthir, of Rennes, a specimen of the magnificent Parnassius imperator from East Tibet ; but when I saw how strongly it resembled P. charltonius of West Tibet in everything but the form of the pouch, whilst this organ was remarkably different, I saw what appeared to me a structural character of the highest value, and was led to an examination of the whole genus, which, on account of the extreme tendency to variation in size, and in the number and colour of the ocelli and markings— which had previously been considered as the principal characters by which to distinguish the species—was in a most unsatisfactory state of confusion. The result of my examination is here given; and I may say that, however faulty and incomplete it may be, I have taken every pains to bring it up to date, and have personally examined the principal collections, both public and private, in Germany, France, Russia, and England. I have thus been able to see, and to a certain extent compare, large numbers of almost all the known species, and though my conclusions may not be accepted by those whose interest and pleasure it is to multiply synonyms, and thus to increase the diffi- culty of the study of Lepidoptera, yet 1 believe that as far as it goes it is based upon facts alone. My own collection, a part of which is now shown, contains about 400 specimens of the 23 species which I recognize in the genus, and includes both sexes of every described species except two. Though this number may seem large, yet I believe that it is not more than half of what would be required to illustrate perfectly such variable species as are most of the Parnassii, and though I have a long series of many, I have kept no specimens which are not necessary to illustrate some fact either of geographical distribution, of variation, or of range of altitude and season. Andsuch I imagine should be the object of every scientific collector in any branch of natural history. We too often see, in British collections at least, a fixed number of specimens exhibited in order to complete a row ; but it is evident that whereas in some species of restricted habitat and little or no tendency to variation, two or three pairs may be 8 MR. H. J. ELWES ON THE GENUS PARNassius. (Jan. 19, ample, in another 100 pairs may be insufficient to illustrate all the points in the history of a species. With respect to the development and function of the pouch in this genus, which appears to me interesting not only to lepidopterists but to all pissisnis of Biology, I must here acknowledge the assistance I have received from Mr. afin Thomson, of the Society’ s Gardens—who undertook and carried out in a most painstaking manner the ecbser- vations on living insects, of which an account is given below— and especially to Mr. Salvin and to Prof. Howes, of the Biological Laboratory, South Kensington, who undertook the difficult an delicate task of dissecting and examining the specimens preserved by Mr. Thomson at the Gandena And though much remains to be done before we can say that we fully understand this intricate question, yet a distinct advance has been made on our previous knowledge, and certain facts which were previously doubtful or obscure have been proved. The first writer who seems to have paid much attention to this organ was Von Siebold, who published in the ‘ Zeitung fiir wissenschaftliche Zoologie,’ 1850, iii. pp. 54—61, and reprinted in the ‘Stettiner entomologische Zeitung’ 1851, pp. 176-185, a long and most valuable paper on the subject, a précis of which, from an English translation kindly lent me by Mr. Gosse, I am here able to give :— The first part is historical, and shows that though Linnzeus, Latreille, and Schiffer had mentioned the existence of the pouch and described its form more or less incompletely in P. apollo and P. mne- mosyne, Do one had carried these observations any further. Ochsen- heimen accepts its existence in the female as a generic character of Doritis, and Boisduval separates Doritis apollinus from Parnassius because it has no pouch. Siebold doubted whether the organ really formed part of the body, as he found that he could easily separate it in P. mnemosyne, and, with more difficulty, in P. apollo, as in this species it is glued more strongly by its base to the underside of the abdomen. He then suggests that it originates during copulation, in these words :—‘‘ Probably from the male or female individual, at the anal region there is secreted a clammy coagulable fluid, poured forth during the close association of the genital organ of the male with that of the female, which, by coagulating and hardening, produces a firm and long-enduring union of both sexes. After the end of the copulative act, and after the complete severance of the sexes, there remains this coagulated substance as a sort of cast or impress of the hinder parts of the male in the vicinity of the sexual orifice of the female, a witness of the accomplished coitus.’ He then states that virgin females fresh from the pupa have no pouch, and says that Hoger was mistaken when he suggested that the pouch was after- wards protruded from the body for the purpose of oviposition. He then goes on to state that a chemical examination of the substance of the pouch by Dr. Baumert showed that it had no affinity with the chitinous substance of the body of the insect, which was insoluble when treated with caustic alkali; whereas the pouch of both P. apollo 1886. ] MR. H. J. ELWES ON THE GENUS PARNASSIUS. 9 and P. mnemosyne dissolved when boiled in the same chemical, leaving only brown oily drops. The alkali was then saturated with mineral acid, but nothing organie was separated from it, whence we must conclude that the originally dissolved substance was destroyed. Siebold compares the pouch of P. hardwicket, which he saw in the Vienna collection, with that of P. mnemosyne, from which, how- ever, as I have afterwards shown, it is very different. He also compares the pouch of P. delins with that of P. apollo, and says that it agrees in colour, texture, and shape, wanting only the sharp keel. In this, however, he was mistaken, as I have never seen a specimen of P. delius, or of any species of this group, in which the keel was absent, though in P. jacquemonti, which Siebold could hardly have seen, it is so. He then describes the observations of Herr Reutti, of Freiburg, who undertook the rearing of P. apollo from the larva in order to prove the correctness of Siebold’s views. On May 29 he collected fifty larvee, which had mostly undergone their last moult, on Sedum album. He describes them as being very troublesome to rear, because the larvee, though feeding greedily when placed on the plants, would not return to the food of their own will, owing to the want of sunshine in a room of north aspect. He succeeded, however, in rearing 11 larvae, which went into pupee under plants or stones, and in one case in an angle of the cover of the cage in a slight web of spun threads; “within this the larva hung by the hind feet in the manner of a Vanessa; the pupa, how- ever, lay free in the web.” Reutti succeeded in rearing four pairs of the butterfly, one of which, on July 17 at 1 p.m, united, and remained in coitu until late at night; next morning they were separate, and the female had a perfect pouch; but no observation was made of its formation. Siebold thinks that the keel in the pouch of P. apoélo is produced as follows: “ By observing the male genital organs of P. apollo, it seems to me that the coagulating secretion is poured out under the two lateral valves, which, on the end of the abdomen of the male beneath, keep the proper genitals embraced, so that these latter, after coagulation of the pouch-forming secretion, are found in the interior of the pouch, whilst the valves are pressed against the out- side of the vault of the pouch, and part of the coagulated matter stands out between them as the above-mentioned keel.” Lastly, Siebold quotes Kollar for an extraordinary story about the larve of P. mnemosyne, which are preserved in the Imperial Collection at Vienna, resembling those of P. apollo in habit, colours, markings, and which are ‘not seldom found on recently dead horses in the lower mountain valleys of Austria and Hungary”’!!! On the same evening that this paper was read, I had hoped that Prof. Howes would have been able to give us the result of his exami- nation of the specimens preserved at the Society’s Gardens as here- after mentioned ; but Prof. Howes having been delayed by illuess and press of other work, his observations will form the subject of a later 10 MR. H. J, ELWES ON THE GENUS PARNassivs. {[Jan. 19, communication from him, and he is only able at present to supply the following note :— ‘*The assumption that the pouch of the female Parnassius performs a definite function after copulation, appears in all cases to have been, without doubt, suggested mainly by its scoop-like shape, no less than by its constant characters and relations and its persistence after coition. This assumption originated with Héger, who believed the pouch to have been concerned in oviposition, describing it, in fact, as a veritable ovipositor, ‘zuerst im Hinterleibe dieser Schmetter- linge fertig verborgen.’ V. Siebold’ first successfully disposed of this view, and showed that the structure in question was a secretion, believed by him to be derived from the male, and to be functional in prolonging the coitus*. I cannot agree with him that this is the case, the adhesion of the copulating individuals being assured by the hook-like claspers of the male. The pouch is densest in the vicinity of the female genital orifice, and its detailed structure conforms internally to the ventro-lateral parts of the male genital funnel. In view of this, the fact that it is impossible, in dissection of specimens procured during copulation, to remove the pouch without bringing away the internal generative apparatus of the female, points, to my mind, to a direct connection between that apparatus and the pouch itself. It suggests the probability of an origin of the same from the body of the female, and not of the male as is generally supposed. I cannot accept the view ‘that the pouch is composed of hardened cases of adherent spermatophores,’ * and the only supposition which seems to me thus far possible is that it represents a viscid secretion, poured out most probably by the female during copulation, which—instead of slowly disintegrating or otherwise disappearing, as do similar coagulable and non-coagulable secretions functional among other animals as accessories to the conju- gative act—is hardened on exposure to the atmosphere. It persists as a cast of the male genital apparatus, which may be carried by the female until the day of her death, a token of the consummation of her existence *. **The above remarks apply to P. apollo, one pair of which species, preserved during a copulation of 75 minutes’ duration, I have alone examined. My best thanks are due to Mr. Elwes for these speci- mens and others, upon which I hope shortly to be engaged.” But though to Von Siebold the eredit is principally due of calling attention to this organ, yet no one seems to have carried his obser- vations any further, though Mr. W. H. Edwards, with Dr. Hagen’s assistance, gave a summary of Von Siebold’s paper in the ‘ Butter- flies of North America’ several years ago, and Dr. Burmeister has * Zeitschr. f. Wissensch. Zoologie, vol. iii. 1851; also ‘ Entomolog. Zeitung,’ same year. 2 Loc. cit. p. 55. % Macalister, ‘Introduction to Animal Morphology,’ vol. i. p. 412, 1876. Prof. Macalister informs me by letter that his material was in a “ very dilapi- dated state.” 4 Conf. y. Siebold, /. ¢. p. 56. 1886.] MR. H.J. ELWES ON THE GENUS PARNASSIUS. 1] in the allied genus Zuryades proved Von Siebold’s ideas to be in the main correct. Burmeister, in his ‘ Atlas de la République Argentine,’ Livr. J, p- 10, pl. 3, figures and describes the structure of the abdomen in Euryades duponcheli and E. corethrus, which is analogous to that in Parnassius. He says that the copulation in Zuryades is very protracted, and though he gives no details of the manner in which the appendages of the female are formed, yet he states that the secretion forming them proceeds from the male, in the same manner as in Parnassius. He does not, however, suggest any use for the appendages nor state whether there is any variation in them. From the figures it is clear that they are almost identical in the two species comprising the genus. Dr. Hagen, in the ‘Comptes Rendus Ent. Soc. Belgique,’ vol. 18, p- lvi, says that he is convinced that the appendage of Furyades is an analogous structure with the pouch of Purnassius, and that the only difference is one of form, which may be easily understood if one allows that the fluid which composes it is emitted on the two sides during copulation. Burmeister, in Stett. ent. Zeit. 1874, p. 427, says of Huryades, that he is convinced that the female appendages of this genus are not developed before copulation, and that the substance of which the apparatus is composed is completely homogeneous with that of Parnassius. He suggests that the secretion flows from the male during the act of copulation, and hardens-afterwards in the form which it took during its exudation from the male’s body. Though there was every reason to believe that Reutti’s observa- tions, as far as they went, were accurate, yet wishing not only to un- derstand more fully the manner in which the ponch was formed, but also its function in the life of the insect, I went in 1884 and 1885 to the Alps to study the question, where the insects are abundant ; but owing to various difficulties, which are detailed in my account of the life-history of P. apollo, delius, and mnemosyne, I failed in observing for myself the necessary details. I was, however, fortunate in procuring through Herr Heine, of Leipzig, a number of pupz of P. apollo, which were sent to the Insectarium of the Zoological Gardens, and have afforded ample details as to this species. Mr. Thomson’s notes are here printed verbatim, but I was able to gather some further details which are worthy of note. He found that Parnassius apollo requires about an hour after emerging from the pupa, in order to perfect and harden the wings, and that the colour of these is at first of a yellowish tinge, but soon fades to white when exposed to the sun. This yellowish tinge I may add is found in some very fresh examples of almost all the species, and may be taken as an indication that the insect is only just out of the pupa. He found that the copulation of the sexes takes place immediately after the complete development of the insects, provided that the sun is bright and warm, but that on dull days the insects remain 12 MR. H. J. ELWES ON THE GENUS PARNAssIvs. (Jan. 19, torpid without flying; that the duration of the act is from 33 to 63 hours, but the pouch is developed in a much shorter time, thirty minutes in one ease sufficing to make it visible to the naked eye. But my observations of P. mnemosyne makeit evident that either that species differs from P. apollo in this respect, or that instances of imperfect copulation, not followed by the appearance of a pouch, may occur. Mr. Thomson also proves: —That eggs may be and are sometimes laid before the completion of the act, and that they may be laid by pouchless females of P. apollo, as I found was also the case with P. mnemosyne. That laying continues for several days at intervals, the life of the female extending to at least a week, whilst the males appear completely exhausted by the act of copulation, and die in one or two days after it without flying much, though they remain lively and strong for several days before the act takes place. No attempt was made by virgin males observed by Mr. Thomson to mate with an already mated female, but my own observations in nature show that this is not the case in a natural state. The date of emergence from the pupa is usually two or three days earlier in the male than the female, and the proportion of males not much greater than of females. But in a wild state the proportion of males of both P. apollo and P. delius always seems to be much greater ; and from the compara- tive rarity of the females in almost all the species of the P. apollo group this seems to be the case in other countries. But in the P. mnemosyne and P. delphius groups females, though occurring somewhat later, seem usually to be nearly as abundant as males. Notes on the Copulation of Parnassius apollo. By Artuur THomson. “On the 18th of June, 1885, I received forty pupz of Parnassius apollo, which had been sent to the Gardens by order of Mr. H. J. Elwes, F.Z.S., for the purpose of watching the perfect insects when copulating, and to endeavour, as far as possible, to throw some light upon the development of the ‘horny pouch’ with which the female is provided after copulation. ‘«* How far I have been successful I must leave others to judge, but I wish to say that the fact of the female Parnassius developing such a ‘pouch’ after emerging from the chrysalis was quite new to me, so that I had no preconceived ideas upon the subject, and I have noted the facts just as they occurred. “{ first had a large gauze cage made, and placed in it six plants of Sedum telephium, the food of this species, and put in the insects as soon as they were ready, after emerging from the pupe. “The first and second copulations took place on June 27; the first pairing lasted from 11.10 a.m. to 2.25 p.M.=3 hours 15 minutes, and the second pairing lasted from 11.30 a.m. to 3.0 p.m.=3 hours 30 minutes. The ‘ pouches’ in each case were perfectly developed, and the females began to deposit their eggs upon the gauze within five minutes of their separation from the males. 1886.) MR. H.J, ELWES ON THE GENUS PARNASSIUS. 13 * Whilst the first pair were in copulation I made a sketch (as well as I was able) of the ‘pouch’ as it then appeared (fig. 1), a side view of the ‘pouch’ immediately after separation (fig. 2), a side view of the position of the female whilst laying her eggs (fig. 3), and a back view of the same (fig. 4)’. The ‘pouch,’ as then seen through a magnifying glass, appeared to be about 7%; of an inch long and not quite an eighth of an inch broad, with a very slight central depression the whole length, of adark green colour, and with very minute transverse corrugations. ‘his I found, during the time I was watching them, to be a membranous covering attached to the abdomen of the ma/e, containing a dark green fluid. This mem- brane entirely covered the true pouch of the female, as I observed that the male appeared to be able to contract it, and did several times, so as to expose the ‘pouch’ of the female, which was then quite white; and it has since occurred to me, that this exposure of the ‘ pouch’ might be for the purpose of hardening it a little, as the ‘pouches’ of the females are quite soft during copulation, but soon harden after separation and exposure to the atmosphere, and this leads me to think that this membranous covering of the male is the mould in which the ‘pouch’ is formed during copulation. One thing, however, is certain, that the ‘ pouch’ is developed entirely during copulation. “The third copulation took place on the 28th of June, and lasted from 10.23 a.m. till 12.48 p.m.=2 hours 25 minutes. The pouch was developed. These specimens were dropped into spirits of wine ‘in cop.’; the membrane of the male then began to contract by the action of the spirit, but the insects did not separate. “The fourth copulation took place on the 28th of June, and lasted from 1.15 a.m. till 2.30 p.m.=1 hour 15 minutes; these specimens were then dropped into spirits. The ‘ pouch’ was developed; and I may here mention as a proof that the ‘pouch’ has nothing what- ever to do with oviposition, that the female of this pair laid an egg whilst ‘in cop.’ “The fifth copulation took place on the 4th of July, and after the insects had been in copulation 30 minutes they were put in spirit. The ‘ pouch’ was apparently developed. ** The sixth copulation took place on the same day ; after being in copulation ¢en minutes the pair were put in a cyanide bottle and killed. They separated after death, but no sign of a ‘pouch’ was visible. These specimens were afterwards put in spirits. ‘ Hab. Cooper Creek, at Innaminka, Central Australia (Prof. Rk, ate). Fig. B. Estheria lutraria. Prof. Tate’s specimens include only a single example of this species —a dried empty shell ; apparently somewhat shrunk and distorted. The specific name refers to the Molluscan genus Lutraria, which it rather closely resembles. 2. EsTHERIA PACKARDI, n. sp. (Fig. C.) Valves, seen laterally, subelliptical, beak prominent and situated near the anterior extremity, extremities rounded, the anterior much the wider of the two, dorsal margin straight in the middle, ventral convex ; lines of growth 12-15, not sharply marked. Shell rather 86 DR. G. S. BRADY ON FRESHWATER [Feb. 2, Estheria packardi. Fig. D. Eulimnadia rivolensis. 1886. ] ENTOMOSTRACA FROM SOUTH AUSTRALIA. 87 hard and dense, dark brown (one of the specimens has a broad white marginal band). Length ;°; of an inch; height ,,. Hab. Lake Bonney, River Murray, South Australia; also Fowler Bay, Great Australian Bight (Prof. R. Tate). Genus Evtrmnapta, Packard. (Limnadia, Brongniart, in part.) EULIMNADIA RIVOLENSIS, n. sp. (Fig. D.) Shell membranous, without any lines of growth; seen from the side, subovate, highest toward the front ; anterior extremity broadly rounded, posterior narrow, very slightly rounded ; dorsal margin well arched, almost gibbous, ventral slightly convex ; the dorsal aspect is compressed, ovate, more than thrice as long as broad, tapered and acuminate behind, somewhat more obtuse in front. Length 3,8, of an inch ; height ;?2;, width ,1°,. Very similar to Limnadia antillarum, Baird, but much larger ; differs also in having the eye near the middle of the anterior margin instead of near the dorsal angle, in being without any distinct lines of growth, and in having an evenly rounded (not angulated) anterior margin. This species was found by Prof. R. Tate in company with Limnetis tatei. Inside the valves of a specimen of this Hulimnadia I found on dissection a large colony of a protozoon, possibly Arcella dentata, Ehrenberg, at any rate very closely resembling that species, as figured by Professor Leidy. Family Arpop1p 4, Burmeister. Genus Leripurvs, Leach. LepipuRus viripuLus. (Fig. E, p. 88.) Lepidurus viridulus, Tate, Trans. & Proc. Philosoph. Soc. Ade- laide (1879), p. 136. * Animal, including flap of tail-segment, about an inch long, carapace rounded, elongate-oval, of a brownish-green colour, covering the whole abdomen excepting flap of tail-segment ; keeled toward the extremity, ending in an acute point, lunately notched posteriorly, and sharply and conspicuously hooked on its margin. Front and lateral margins of the carapace smooth and thickened. The rings of the abdominal segments, dark brown, are beset with stout spines equidistantly placed all round and directed backwards. The flap of the tail- segment has a blunt keel along its whole length, with blunt promi- nences, and its edges are ciliately serrated. The filaments of the tail are about half the length of the body, and are clothed with fine cilia. *« Hab. Collected by Thomas Tate, October 1878, in the floodwaters of the ‘ Reedbeds,’ near Adelaide. **Two Australian species of the genus have been described. LZ. vi- ridis, so called from its colour, inhabits Tasmania, and was diagnosed 88 DR. G. S. BRADY ON FRESHWATER [Feb. 2, by Dr. Baird (Proc. Zool. Soe. 1850, p. 254); and L. angasi of the same author, 1866, which is of a pale horny colour, and is common in the rain-pools about Adelaide. ZL. viridis is characterized by its fine green colour, by its oval carapace covering less of the body than in LL. angasi, and the edges of the lower half of its length being serrated ; L. angasi is distinguished by its horny colour, its rounded carapace Fig. E. Lepidurus viridulus. covering nearly two thirds of the body, and by the smooth edges of the sides of the carapace. “ L. viridulus differs from Z. angasi in colour, in the carapace covering more of the abdomen, its keel limited to the hinder part and in the narrower and more spathulate tail-flap.” —Trans. & Proc. & Report of the Philosophical Society of Adelaide, South Australia, for 1878-9, p. 136 (published 1879), afterwards called the Royal Society of South Australia. Order OSTRACODA. Family Cypripip4. Genus Cypris, Miiller. 1. Cypris virn1puLA, n. sp. (Plate VIII. figs. 1, 2.) “ Carapace oblong, compressed, reniform, greatest height situated in the middle, and somewhat less than half the length; seen from the side the extremities are well rounded, the anterior somewhat the narrower of the two, dorsal margin almost flat or very slightly arched, ventral sinuated in the middle ; seen from above, compressed, ovate, twice as long as broad, widest in the middle, gradually tapered towards the anterior extremity, which is subacuminate, posterior extremity narrowed and rounded ; surface smooth and polished, the 1886.] ENTOMOSTRACA FROM SOUTH AUSTRALIA. 89 anterior half marked with a fine reticulated sculpture, colour greenish, clouded with bands of a darker shade. Length 5); of an inch. Collected by Mr. Thomas Steel at Condong, on the Tweed River, near Sydney, New South Wales, 2. Cypris sTANLEYANA (King). (Plate VIII. figs. 3, 4.) Candona stanleyana, King, 1855, Pap. Proc. R. Soc. Van Die- men’s Land, vol. iii. pt. 1, p. 66, pl. x. H. This is very much like C. viridula, but the height is somewhat less, the dorsum is more decidedly arched, and the extremities are less obliquely rounded. The surface is marked everywhere with fine, very closely set, and deep longitudinal grooves. Colour light green, slightly clouded. Length 51, of an inch. Taken in the same gathering as the preceding species. Mr. King refers this to the genus Candona ; but the lower antenna is provided with a brush of sete reaching about to the extremity of the terminal claws. 3. Cypris TATEI, n. sp. (Plate VIII. figs. 5, 6.) Shell, seen from the side, broadly reniform, greatest height in the middle, and equal to more than half the length; extremities rounded, dorsal margin boldly arched, sloping abruptly behind, more gradually towards the front, ventral deeply sinuated in the middle; seen from above, the outline is ovate, somewhat compressed in front, widest behind the middle, anterior extremity subacuminate ; posterior wide and rounded; valves unequal, that of the right side the larger. Surface smooth, colour yellowish brown, with darker clouded markings. Length = of an inch. Taken by Prof. R. Tate in “brackish pools in a dry creek at Adelaide.” This species, though considerably more tumid, has very much the general character of C. prasina, Fischer (fretensis, Brady & Robert- son), and of C. incongruens, Ramdohr, especially as to the curiously compressed anterior extremity. It is remarkable, too, that all of these are inhabitants, almost exclusively, of brackish water. I have pleasure in naming the species after Prof. Ralph Tate, by whom it was found, and to whose kindness I am indebted for the opportunity of describing it. 4, Cypris MYTILOIDES, n. sp. (Plate IX. figs. 1-3.) Shell, seen laterally, elongated, siliquose, highest in front, pro- duced behind into a very acute, tapering beak ; height equal to less than one half the length; anterior extremity broad and boldly rounded, dorsal margin boldly arched, highest near the front, thence sloping at first with a gentle curve, but more abruptly towards the posterior extremity, in front of which it is deeply sinuated ; ventral margin almost straight, with a slight median sinuation; seen from above, compressed, oblong, widest near the middle, about thrice and a half as long as broad; extremities acute, the posterior the more 90 DR. G. S. BRADY ON FRESHWATER [Feb. 2, slender of the two. The right valve is the smaller of the two, and has the dorsal margin less arched. The inner aspect of the valves shows a large shelf-like flange fore and aft. The terminal claws of the second pair of antennz are slender and finely pectinated on the inner margin. Postabdominal rami slender, with one long terminal claw, one short seta at the base of the claw, and one a little removed on the margin of the ramus. Margins of claws and ramus minutely pectinated. Shell thin, horny, of a smoky hue. (“Colour in life light-brown, with darker zebra-like markings.’ Prof. 2. Tate.) Length J of an inch. ; Collected by Prof. R. Tate in fresh water, at Kangaroo Island, Australia. Though quite abnormal in shape of shell, the soft parts of the animal agree in every important respect with those of the genus Cypris. Genus CHLAMYDOTHECA, de Saussure’. ‘Testa undique pilosa, antice posticeque rotundata, appendice anteriore cum margine valvulz dorsali sensim coalescente, cum mar- gine ventrali autem angulum manifestum efficiente; appendice posteriore minima. Altitudo maxima pone medium et propius ventralem quam dorsalem marginem sita, exinde pars postica crassior quam antica. Margo ventralis vix sinuata, dorsalis valde armata. Impressio muscularis paulo ante medium sita.” The anatomical structure agrees exactly with Cypris. The author (de Saussure) refers to a paper by Sir John Lubbock, in which a similar species, Cypris brasiliensis, is described *. The genus Cypridea, Bosquet’, if not identical with, is at least very nearly allied to, the forms now under discussion. No undoubted recent specimens of Cypridea have, however, as yet been seen, and Prof. Rupert Jones, in a recent paper “ On the Ostracoda of the Purbeck Formation,’ * says that the “hinder margin is definitely straight along the middle third or more of the dorsal edge, with the hinge-angles more or less defined, and is oblique to the main axis of the valve. The left valve is the largest, and receives the dorsal edge and a straight ridge of the other valve in grooves on its dorsal and ventral contact-margins.”” These characters are not to be found in Chlamydotheca. Moreover, from the figures given by Prof. Rupert Jones, it seems that both valves of Cypridea are provided with the notch and hatchet-like anterior process, whereas in Chlamy- dotheca only the left valve is so formed. 1 “ Mémoire sur divers Crustacés nonveaux des Antilles et du Mexique,” par M. Henri de Saussure. (Mémoires de la Société de Physique et d'Histoire Natu- relle de Genéve, 1856.) 2 “On the freshwater Entomostraca of South America.” (Trans. Entom. Soe. Lond. new series, vol. iii. part vi. 1855.) 3 “Hntom. fossil. des Terrains tertiaires de la France et de la Belgique.” (Mém. couronnés Acad. Royal de Belgique, vol. xxiv. 1852.) 4 “ Ostracoda of the Purbeck Formation, with notes on the Wealden species.” (Quarterly Journal of the Geological Society, August 1885.) 1886. ] ENTOMOSTRACA FROM SOUTH AUSTRALIA. 91 CHLAMYDOTHECA AUSTRALIS, 0. sp. (Plate IX. figs. 4-8.) Shell, seen from the side, subovate, greatest height equal to rather more than half the length, and situated in the middle, anterior extremity rounded, produced at the inferior angle so as to forma ventral beak, posterior extremity narrower, rounded, dorsal margin boldly arched, ventral slightly sinuated in the middle, more deeply in front, behind the beak ; seen from above, the outline is ovate, twice as long as broad, anterior extremity forming a large, broad, obtusely-pointed, and twisted prominence, posterior slightly narrowed and produced, but rounded off. The valves are unequal, the left being the larger, overlapping on the ventral, and less distinctly on the dorsal margin. The outline of the right valve is more evenly rounded than that of the left, presenting no ventral beak nor sinua- tion, nor are the margins, either ventral or dorsal, so much incurved ; the inner aspect of the valves shows shelving flanges both before and behind, and in that of the left side there is a curious twisted ridge separating the anterior beaked portion from the body of the shell. The substance of the shell is rather thick ; surface closely marked with small circular impressions ; colour fuscous. Length +1, of an inch. The specimens are all empty shells, so that the structure of the soft parts is as yet unknown. Penola (Prof. R. Tate). Genus Cypripopsis, Brady. 1. Cypripopsis minna (King). (Plate X. figs. 1-3.) Cypris minna, King, 1855, Pap. Proc. R. Soc. Van Diemen’s Land, vol. ili. pt. i. p. 64, pl. x. B. Shell very tumid; width and height about equal, length about one fourth greater. Seen from the side, subcircular, highest in the middle, extremities broadly rounded, dorsal margin excessively arched, ventral nearly straight in the middle; seen from above very broadly ovate, obtusely pointed in front, the hinder part forming almost a complete circle; end view subcircular, obscurely pointed above, slightly keeled and emarginate below. Surface smooth, beset with small impressed circular puncta; colour olivaceous, clouded irregularly with darker patches. Anterior margins of the valves slightly crenulated. Length ;\ of an inch. flab. Condong River, Australia (Mr. T. Steel). ‘« Ponds, every- where” (Rev. R. L. King). 2. CYPRIDOPSIS FUNEBRIS, n. sp. (Plate VIII. figs. 7-9.) Shell, seen from the side, subtriangular ; greatest height a little in front of the middle and equal to nearly two thirds of the length; extremities rounded, the anterior wide, posterior narrower and not so well rounded, dorsal margin elevated and almost gibbous near the middle, thence sloping almost in a straight line backwards, and with a gentle curve towards the front, ventral almost straight ; seen from above, ovate, widest in the middle, width equal to two thirds of the 92 DR. G.S. BRADY ON FRESHWATER ENTOMOSTRACA. [Feb. 2, length, anterior extremity obtuse, scarcely rounded, posterior rounded off and rather wider than the front. End view subcircular. Surface smooth, cream-coloured, with transverse black bands after the manner of C. vidua. Length =\, of an inch. Hab. Condong, Tweed River, New South Wales (Mr. T. Steel). Genus Noropromas, Lilljeborg. (Newnhamia, King, 1855, Pap. Proc. R. Soc. Van Diemen’s Land, vol. ili. pt. 1, p. 67.) NoToDROMAs FUSCATUS, n. sp. (Plate X. figs. 4-6.) Shell, seen laterally, subtriangular, height equal to three fourths of the length, extremities very broadly rounded, the anterior some- what the narrower of the two, dorsal margin excessively arched, highest a little behind the middle ; ventral nearly straight ; seen from above, the outline is ovate, scarcely twice as long as broad, tapered and acuminate in front, rounded off behind. Surface of the valves somewhat rough and furfuraceous, colour brownish, with darker cloudings. The ventral aspect of the shell is ribbed almost exactly asin N. monachus; the “ ocular”’ tubercle is large and distinct ; by transmitted light the shell is seen to have a polygonal reticulated structure, and the reticulations are visible also by reflected light on the anterior portion of the valves. Hab. At Condong, with the foregoing species. This is very much less tumid and less angular in outline than Newnhamia fenestrata, King, and its lateral outline differs in the same way from Notodromas monachus, Miiller. Genus Canpona, Baird. 1, Canpona LuTEA, King. (Plate X. figs. 7, 8; &? Plate VIII. figs. 10, 11.) Candona lutea, King, 1855, Pap. Proc. R. Soc. Van Diemen’s Land, vol. iii. pt. i. p. 67 pl. x. kK. Male. Shell, seen from the side, subreniform, depressed in front, greatest height near the posterior extremity and equal to half the length ; anterior extremity narrow and well rounded, posterior wide, obliquely rounded ; dorsal margin forming a flattened arch, sloping with a gentle curve to the front, and abruptly backwards, ventral sinuated in the middle ; seen from above, compressed, ovate, about thrice as long as broad, gently tapered towards the front, which is subacuminate, rounded off behind. Shell smooth and _ polished, pellucid, white or straw-coloured. Length > of an inch. Hab. Condong, with the foregoing species. The shell figured in Plate VIII. figs. 10, 11, occurred in the same gathering, and possibly may be the young of C. lutea. 2. CANDONA TENUIS, n. sp. (Plate X. figs. 9, 10.) Shell elongated, compressed, reniform ; seen from the side it is at least twice as long as broad, the greatest height being a little behind the middle, extremities rounded, dorsal margin boldly arched, ventral P. Z.5.1886. PL VII. / | 10 4 Geo West & Sons, hth etimp. NEW AUSTRALIAN ENTOMOSTRACA. G.S.B. del. PZ.S, 1886. PLT: Geo West & Sons, lith et imp. NEW AUSTRALIAN ENTOMOSTRACA. i =o Ago Pelt} | Yan al DG Geo.West & Sons lith etimp. G.S.B. del. NEW AUSTRALIAN ENTOMOSTRACA. 1885.] DR. MONTICELLI ON SOUTH ITALIAN CHIROPTERA. 93 deeply sinuated in the middle ; the dorsal view is elongated, ovate, quite thrice as long as broad, widest in the middle; extremities narrowed, the anterior subacuminate, posterior rounded off; left valve rather larger than the right. Shell smooth, pellucid, cream- coloured, with opaque cloudings. Length 35 of an inch. Taken in company with the preceding species. EXPLANATION OF THE PLATES. Pzarr VIII. Fig. 1. Cypris viridula (p. 88), seen from left side. thy VER ” seen from above. x 40 3. ,, stanleyana (p. 89), seen from left side. < ow ics i seen from above. 5. ,, tate? (p. 89), seen from left side. x 20 Ga* ts; ,, seen from below. + 7. Cypridopsis funebris (p. 91), seen from left side. 8. 4 45 seen from above. x 40. 9. 5 e seen from front. } 10. Candona lutea, jun. ? (p. 92), seen from left side. \ x 80 Lal , “s seen from above. j = Prats IX. Fig. 1. Cypris mytiloides (p. 89), seen from left side. “6 2. A 3 seen from above. ; o. br fs postabdominal ramus. x 40. 4. Chlamydotheca australis (p. 91), seen from left side. 5. a PA seen from below. 6. 6 5 seen from front. * 28. ic MY 55 left valve seen from inside. 8. 3 : right valve seen from inside. ) Puate X. Fig. 1. Cypridopsis minna (p. 91), seen from right side. 2. +s », seen from below. x 40. 3. 5 », seen from front. 4, Notodromas fuscatus (p. 92), seen from left side. 40 5. “A Ay seen from below. pe 6. he 5 shell structure. x 400. 7. Candona lutea, male (p. 92), seen from left side. 8. A 3 seen from above. 40 9. _ tenuis (p. 92), seen from left side. — 10. F » seen from above. 2. Contribution to a Knowledge of the South-Italian Chiroptera. By Fr. 8. Monricexur, D.Sc. (Commu- nicated by Dr. H. Woopwarp, F.R.S., F.G.S.) [Received January 5, 1886.] Bonaparte’ was the first naturalist who wrote upon Italian Chiroptera; but his researches are tvo general, and there are no indications of southern localities contained in his work. Later on, Prof. C. G. Costa gave in 1839* a catalogue of 1 «Teonografia della Fauna Italica’: Roma, 1832-41. * *Flenco dei Mammiferi e Supplemento.’ (Fauna del Regno di Napoli.) 94 DR. MONTICELLI ON SOUTH ITALIAN CHIROPTERA. [Feb. 2 Chiroptera of the kingdom of Naples; but after him, excepting Major ', who announced the discovery of Vesperugo Jeisleri in South Italy, no one else has written about the Chiroptera of this country. Quite recently, however, Camerano and Lessona* have given notices of some of the Southern species. Prof. Costa’s work in 1839 enumerates the following species:—hinolophus bihastatus, Vesperugo serotinus, Vespertilio bechsteinii, Vespertilio murinus, Dysopes cestoni, Plecotus auritus, and Myopterus daubentoni. From this catalogue of Costa must be excepted V. bechsteini, which I have not yet met with, and Myopterus daubentoni, which is not a European species ; but there are to be added thirteen other species, so that the number of Chiroptera of South Italy now consists of at least eighteen species. Amongst the thirteen species to be added to the catalogue of Costa there are many very important as regards the geographical distribution of the different species in Italy ; such as Synotus barba- stellus, which so far has only been found in Northern Italy ; and also a species altogether new to Italy, which I have recently described as Vespertilio oxygnathus. I am preparing descriptions, carefully compiled, of all the South- Italian Chiroptera ; but for the present I give this preliminary cata- logue of them, with indications of the localities where they are found. 1. Nycrrnomus CESTONI, Savi. This species does not seem to be common in the South, but it is not rare at Naples. I have not been able to procure specimens from other points of the Mediterranean side of Italy, but it is possible that it may be found on the Adriatic side, where so far no researches have been made. 2. RHINOLOPHUS FERRUM-EQUINUM, Schr. This species is very common, and easy to find anywhere. 3. RHINOLOPHUS EURYALE, Blas. Although Camerano and Lessona say this species is less common than the preceding, and is found particularly in North Italy, I have also found it equally distributed in South Italy. 4. RHINOLOPHUS HIPPOSIDEROS, Bechst. Less common than the preceding, but not rare. I have not met with R. blasii, Peters, although Blasius says that he found it in Middle and Southern Italy and Sicily, and Camerano obtained it in Sardinia. 5. MINIOPTERUS SCHREIBERSI, Natt. Very common throughout the whole of South Italy. 1 “Vertebrati Italiani nuovi o poco noti”: Atti Soc. Tose. Natur. Pisa, vol. iii. 1876. 2 *Compendio della Fauna Italiana’: Torino, Loescher, 1885. 1886.] DR. MONTICELLI ON SOUTH ITALIAN CHIROPTERA. 95 6. PLecorus auritus, Linn. This Bat seems to be more common on the Adriatic than on the Mediterranean side of Italy. 7. SYNOTUS BARBASTELLUS, Schreb. This species has been hitherto said to be found only in North Italy. It occurs also in South Italy. 8. VESPERUGO (VESPERUS) SEROTINUS, Schr. This species is not very frequently observed, but is found everywhere, 9. VESPERUGO NocruULA, Schr. Not common in South Italy, but not rare. Up to the present time it has been found only on the Adriatic side. 10. VEspERUGO LEISLERI, Kuhl. A very rare speciesin Italy. There are only two specimens in the Museum of Florence, which were obtained in the province of Lecce. 11. VespervuGo savu, Bp. This Bat is very common everywhere. 12. VesPERUGO KUALI, Natt. Very common everywhere; found both in town and country. There are many variations in the colour and size of specimens; I have found some all white, and others black. These may be con- sidered as two distinct varieties: the former I call “ var. albicans,” the latter “ var. pudlatus.”’ 13. VESPERUGO PIPISTRELLUS, Schreb. A species common everywhere. In some places it is met with in great numbers. 14. VEsPERTILIO BLASII, Major. Vespertilio majori, Ninni, Fauna Venet.' Up to the present time a very rare species. I have seen only one specimen, which is in the collection of the Zoological Museum of Naples. 15. VESPERTILIO MURINUs, Linn. Generally distributed over the whole of Southern Italy. 16. VESPERTILIO OxYGNATHUS, Mont.? I have founded this new species on specimens found at Matera (province of Basilicata). It is very closely allied to V. murinus, but is at once distinguished by the ears, which are as long as the head, the great development of the glands of the muzzle, by the ' «Materiali per una Fauna Veneta’: Venezia, 1878; Atti R. It, Venet. * Ann. Ace. Or. Costa d. Asp. Natur. Era 3, vol. i., con tayola. 96 MR. SHARPE ON BIRDS IN THE HUME COLLECTION. [Feb. 2, acutely pointed muzzle, and the prominent nostrils, which open sublaterally, as also by the small upper premolar, the form of the ear, the tragus with a distinct lobe at the base of outer margin, and by its small feet. The wing-membrane does not extend so far outwards along the foot, and its colour is darker. This new species has also many characters common with V. afri- canus, Dobson, V. dobsoni (murinoides), and V. chinensis. 17. VESPERTILIO EMARGINATUS, Geoffr. In the Museum of Florence there are many specimens of this species found in different localities of South Italy, but I have not succeeded in procuring other specimens. 18. VESPERUGO NATTERERI, Kuhl. This species does not seem to be very common. I know of only two specimens from the South. The following Italian species of Chiroptera I have not yet found in the South :— . Rhinolophus blasii, Blas. . Vesperugo nathusii. . Vesperugo discolor. . Vesperugo leucippe. . Vespertilio daubentoni. Vespertilio mystucinus. . Vespertilio bechsteinit. NEO OB CoN Naples, Noy. 1885. 3. Notes on Specimens in the Hume Collection of Birds. By R. Bowpier Suarrg, F.L.S. &e. No. 1. On the Hawfinch from Attock. [Received January 14, 1886.] Three specimens of a Hawfinch were collected at Attock in the Punjab, in March 1869, and in February 1870, by Colonel Delmé- Radcliffe. They are mentioned by Mr. Hume in ‘ The Ibis’ for 1869, p- 456, and again in ‘Stray Feathers’ for 1877, vol. vii. pp. 413, 462, and are there referred to C. vulgaris, i. e. C. coccothraustes (Linn.). In the Hume Collection there were no specimens of true C. cocco- thraustes from Europe ; and the comparison of these specimens was therefore doubtless made with plates of the European bird; but on comparing the three birds with a series of true C. coccothraustes, it seems to me certain that they are distinct from the European Haw- finch. The female differs from the corresponding sex of C. coccothraustes in being ochreous brown above, pale ashy ochreous on the lower 1886.] ON ISOPODA COLLECTED BY H.M.S. ‘CHALLENGER.’ 97 back, rump, and upper tail-coverts, while the crown of the head is ashy grey like the hind neck ; sides of face also ashy grey washed with ochreous; breast and sides of the body ochreous buff, instead of vinaceous brown; centre of breast and abdomen white. Total length 6°75 inches, culmen 0°75, wing 3°9, tail 2°35, tarsus 0°8. The male differs less from C. coccothraustes than the female, but it is distinguished by its paler coloration, and by the breast and sides of the body being light orange-brown instead of vinaceous. Total length 6°9 inches, culmen 0°8, wing 3°8, tail 2-1, tarsus 0°8. I may add that the Attock bird is not CO. japonicus, for it has a greater extent of pure white on the wing-coverts than in even true C. coccothraustes. C. japonicus is scarcely to be distinguished from the European bird; and differs only in having the median and greater wing-coverts pale drab at the ends instead of white. I propose to call the Coccothraustes from Attock after my friend Mr. Hume, C. humii. Whether it is the Hawfinch recorded by Lieut. Barnes as a permanent resident at Chaman in Southern Afghanistan (Str. F. ix. p. 456) must remain a question to be decided by an examination of specimens, which I have not yet had the opportunity of doing. 4, Preliminary Notice of the Isopoda collected during the Voyage of H.M.S. ‘Challenger.’—Part III. By Frank E. Bepparp, M.A., F.R.S.E., F.Z.S., Prosector to the Society. [Received January 25, 1886.] The present paper completes the preliminary description of the new species of Isopoda collected during the voyage of the ‘ Challenger.’ This paper includes the families Munnide, Asellide, Arcturide, Cymothoide, Spheromide, Tanaide, Anceide, and Anthuride, of all of which there are specimens in the ‘ Challenger’ collection, representing about 45 new species, besides a number of others previously known. Among the shallow-water species the largest number of new forms are from Kerguelen, in spite of the investigations into the marine fauna of that region carried out by the British ‘Transit of Venus Expedition,’ and the exploring voyage of the German S.S. ‘Gazelle.’ I have to add quite as many new species as those previously known to the fauna of Kerguelen and the adjacent islands (Prince Edward’s Island, &c.). Among the deep-sea species the most remarkable and interesting is undoubtedly a new genus of Cymothoade, which is described below under the name of dAnuropus branchiatus; there are also numerous representatives of other deep-sea forms, as might be expected from the nature of the explorations carrried out by the ‘ Challenger * Published by permission of the Lords Commissioners of the Treasury. Proc. Zoou. Soc.—1886, No. VII. 7 98 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, Fam. MuNNID2. Genus Munna, Kroyer. 1. MuNNA MACULATA, 0. sp. A single male example of this species was dredged in shallow water at Kerguelen. It measures about 4 millim.inlength. The body is smooth, and the integument has numerous black pigment-spots. The shape of the body is characteristically that of a female, being broader anteriorly than posteriorly ; the head is about as long as the first two segments of the thorax; the anterior margin is straight and fringed with a row of stiff hairs; the eye-stalks are well developed. The four anterior segments of the thorax are subequal ; the three posterior are narrower ; the thoracic segments have short rounded epimera. The antennules consist of a four-jointed peduncle, the two distal joints of which are much shorter than the proximal joint ; the flagellum consists of four joints, which are elongated and narrow. The antennz are very long, about twice the length of the body; the flagellum is shorter than the peduncle: the last two joints of the peduncle are elongated and subequal. Kerguelen, 25 fathoms. 2. MUNNA PALLIDA, 0. sp. This species, like the last, is represented by a single male specimen, measuring rather lessthan 3 millim. Like other species, the male is of approximately uniform diameter throughout. ‘The species is pale and transparent, without any trace of pigment. The head terminates in a truncated anterior margin; the eyes are sessile—not stalked. The first segment of the thorax is longer than any of the three following, which are subequal; their margins are rounded and furnished with small rounded epimera; the three posterior segments are curved backwards ; the first is very short, the rest increase slightly in length progressively. ‘The abdominal shield is oval, ending in an obtusely rounded extremity. The antennules are like those of the last species, but the flagellum is only three- jointed. Kerguelen, 30 fathoms. Genus IscuNosoma, Sars. 1. IsCHNOSOMA BACILLUS, 0. sp. This species is only represented by a single fragment, including the abdomen and four last thoracic segments, which is, however, sufficient to determine with at least probability its systematic position ; it measures | millim. The fourth and fifth segments of the thorax, as in Sars’s species, are closely connected and form an hourglass-shaped structure, the two pairs of appendages belonging to these segments being placed at each extreme of the conjoined segments. The fourth and fifth segments are each provided with long spine-like epimera. The presence of spines upon the fifth segment of the thorax distinguishes this species from both I. dispinosum and I. quadri- 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 99 spinosum, and from the next species I. bacilloides. The specimen is a female. Station 158; 1800 fathoms. 2. IsCHNOSOMA BACILLOIDES, 0. sp. This species is closely allied to the preceding, but presents certain differences which appear to necessitate its separation as a distinct species. The single specimen is a fragment consisting of the same segments as J. bacillus, save for the fact that the fourth segment of the thorax is incomplete; unlike the foregoing species, it is a male ; hence the supposed specific difference may be sexual. This species is to be distinguished from J. bacillus by the fact that the sixth segment of the thorax as well as the fifth has a pair of lateral spines. In both species the uropoda are simple, each consisting of two joints. Station 302; 1450 fathoms. 3. IscHNOSOMA SPINOSUM, N. sp. This species is more closely allied than either of the foregoing to Sars’s two species Ischnosoma bispinosum and Ischnosoma quadri- spinosum, and, like them, comes from the Northern Hemisphere. The single specimen measures 6 millim. in length. The general shape of the body is similar to J. guadrispinosum; the head is narrower and shorter than the first segment of the thorax ; there is no trace of eyes. The first segment of the thorax is larger than either of the two succeeding, which are subequal ; the fourth segment is much longer and broader anteriorly than posteriorly, where it is closely applied to the fifth segment, which is the longest of all; the sixth and seventh segments are short. The whole of the dorsal surface of the thorax is roughened and tubercular; the lateral margins of the first three segments are furnished with two or three longish stout spines, of which one on each side is particularly long ; the dorsal region of these segments is not only tubercular but furnished with a few longish spines; tbe fourth segment has no long lateral spines like those of the preceding segment; the remaining thoracic segments have likewise no lateral spines. Between the thorax and abdominal shield is a single free abdominal segment; the anterior half of the latter is oval; there is a deep notch behind this, just in front of the articulation of the uropoda, which are borne upon a short truncated process ; the extremity of the abdominal shield is prolonged for some way behind the uropoda, and terminates abruptly in a straight margin. The abdomen is roughened and tubercular like the rest of the body ; there is a row of short spines on either side of the dorsal median line. Station 78; 1000 fathoms. ASTRURUS, Nov. gen. This genus comes near to Pleurogoniun, Sars, but may be distin- guished by the spiny body, the long bifid rostrum, and the long epimeral spines, which are themselves covered with shorter spines ; 7* 100 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, the thoracic appendages are slender and not greatly elongated ; they terminate in a single claw; the first pair are subcheliform. The uropoda are rudimentary, consisting of only a single conical setose joint. 1. ASTRURUS CRUCICAUDA, N. sp. This species is represented by a large number of individuals dredged in shallow water off Kerguelen ; the largest individuals only measure 4 or 5 millim. in length. The body is more or less pear-shaped, the anterior region of the thorax being wider than the posterior. The head is narrower than the succeeding segment of the thorax ; it is prolonged anteriorly into two long slightly divergent processes, each of which is as long as the head itself ; laterally is a longish process on either side, which terminates in a slightly swollen extremity ; ; these processes resemble the eye-stalks in Munna, and they contained some orange-coloured pigment in the interior, but no recognizable trace of lenses ; the surface, moreover, is covered with numerous short spines like the rest of the body. The four anterior thoracic segments are of nearly equal length, but they increase in width up to the third; the median region of these segments is convex and densely covered with short spines; the lateral margins are prolonged into long stout spines, which are themselves covered with short spines like the thoracic segments and the rest of the body. The three posterior segments are all much shorter than the fourth segment, and decrease gradually in length; their lateral margins are without the greatly elongated spines of the anterior segments ; only on the fifth and sixth segments oue of the spines which fringe the body is rather more elongated than the rest. The abdominal shield is oval, tapering posteriorly ; it termi- nates in four somewhat flattened spines arranged in the form of a cross. The antennules consist of a two-jointed peduncle and a five- or six-jointed flagellum ; the proximal joint of the peduncle is broader and shorter than the succeeding joint. The antenne are not so long as the body but considerably longer than the antennules ; the two proximal joints of the peduncle are elongated, the flagellum is shorter than either of these. The mandibles have a three-jointed palp. The first pair of thoracic appendages are modified into a prehensile limb; the remaining thoracic appendages are slender and elongated, particularly the three posterior pairs. The wropoda are rudimentary as in Munna. Kerguelen, 120 fathoms. Neraseuuus, F. E. B. Neusellus, F. E. Beddard, Narr. Chall. Exp. vol. i. p. 882. fir. 326. This new genus is represented by a single species from Kerguelen. It comes near to Pleurogonium and Leptaspidia, but is distinguished by the great horizontal elongation of the head, which is as wide as the following segment and bears the antennary organs at the 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 101 extreme lateral margin; eyes are absent. The thoracic segments are separated by deep incisions; the first segment is much the largest, and is fused mesially with the following segment; the margins of the segments are rounded ; and the whole body is fringed with numerous leaf-like flattened spines. 1. NEASELLUS KERGUELENENSIS, F. E. B., loc. cit. The extreme length of the single individual of this species is 2 millim. The body is extremely flattened and depressed, pear-shaped in general outline, being much broader anteriorly than pos- teriorly. The head is immensely extended laterally, being as wide as the following segment of the thorax, from which, however, it is separated by deep lateral incisions. The central region is convex ; the anterior and lateral margins are fringed with peculiar flattened spines, which also border the body throughout. The two first segments . of thethorax are together about equalin length to the headin its middle region ; the line of suture separating these two segments is obliterated except laterally ; the remaining segments are short and subequal, each is about 1 of the length of the conjoined anterior segments ; the third, fifth, and sixth segments have lateral processes, fringed with the peculiar spines referred to, which are absent from the fourth and seventh segments. The shape of the abdominal shield, which is, as in Pleurogonium &c., separated from the last segment of the thorax by a single free abdominal segment, is rhomboidal; it is notched posteriorly and laterally where the uropoda articulate. The antennules and antenne arise from the extreme lateral margin of the head ; in the antennules the basal joint is short and stout, the second rather elongated, the third and fourth narrower and shorter than the second, the flagellum has two joints. The antenne are more than half the length of the body, the peduncle has six joints, the flagellum is a little longer than the distal joint. The mandibles are furnished with a palp. The first thoracic appendages are cheliform, the remaining thoracic appendages are not greatly elongate. The uropoda are as in Pleurogonium. Kerguelen, Christmas Harbour, 120 fathoms. Genus PLEUROGONIUM, Sars. 1. PLEUROGONIUM ALBIDUM, 0. sp. This species is represented by a single female example measuring 3 millim. The general shape of the body is like the other species de- scribed by Sars; the epimera of the first four thoracic segments are prolonged into spines, which are of equal size upon all the segments; the three posterior segments of the thorax are separated from each other and from the fourth by deep lateral incisions ; their epimera are prolonged into stout spiny processes, which are shorter than in the anterior segments; the dorsal surface of each of these three segments is traversed by a narrow ridge. Between the 102 MR. F, E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, seventh thoracic segment and the abdominal shield is a narrow free abdominal segment, which is ridged like the posterior segments of the thorax. The abdominal shield is almost circular in its outline anteriorly ; posteriorly it terminates in a triangular-pointed extremity ; the posterior region is slightly serrated. Kerguelen, 120 fathoms. 2, PLEUROGONIUM SERRATUM, N. sp. This species, like the last, is represented by a single female example measuring 3 millim. in length. The head is small and almost enclosed by the following segment of the thorax; the frontal margin is straighter than in the last species, and the articulation of the antenne is not so near to the posterior boundary of the head; the hinder margin of the semi- circular notch which lodges the antenne is prolonged outwards into a longish pointed process, which extends laterally nearly as far as the epimeron of the first thoracic segment. The thoracic segments are so like the last species that no special description is needed. The most characteristic and obvious difference between the two species is in the abdominal shield, which has, however, the same general shape in P. serratum as in P. albidum; in the former species the lateral margin as far back as the articulation of the uropoda is strongly serrated ; there is no trace of any such serrations in P. albidum except along the posterior extremity of the caudal shield behind the uropoda, in which situation they are absent in P. serratum. Kerguelen, 120 fathoms. 3. PLEUROGONIUM MINUTUM, 0. sp. The third new species of this genus is represented by a single female example, dredged off Tristan da Cunha. It measures about 1 millim. in length. The general shape of the body is like that of the other species. The epimera of the thoracic segments are not prolonged into spines as in the last two species, but are rounded in the four most anterior segments and truncated in the posterior thoracic segments. The abdominal shield is oval, tapering posteriorly ; anteriorly the margins of the abdominal shield are serrated, but the serrations are not nearly so marked, nor do they extend over so great an area as in P. serratum. In the two last species the antennz are twice the length of the antennules; in the present species they are longer, but only half as long again: in this respect therefore Pleurogontum minutum is more typical, that is to say it agrees more closely with the northern forms described by Sars. Off Tristan da Cunha, 100-150 fathoms. ACANTHOMUNNA, nov. gen. * This genus is like Munna in outward form, and is furnished with a pair of eyes elevated on stalks as in that genus ; the thoracic limbs are entirely like those of Munna except that they terminate in a 1886.] DURING THE VOYAGE OF H.M.S, ‘CHALLENGER.’ 103 single elongated claw ; the antennule has a four-jointed peduncle and a long multiarticulate flagellum ; the uropoda are defective but evidently are of considerable size, judging from the socket of articu- lation. The whole body is covered with short slender spines of varying size, but nowhere very long. 1, ACANTHOMUNNA PROTEUS, 0. sp. This species, the only one referable to the genus, is represented by two individuals, both males, dredged off New Zealand in 700 and 1000 fathoms respectively. The larger specimen measures 7 millim. in length. ‘The general shape of the body is as in Munna, but differs in being covered with innumerable spines, many of which are branched ; the spines are nowhere of very great length. The head is furnished with a pair of eyes situated laterally ; these are elevated upon short stalks ; the abdominal shield is preceded by a short tree abdominal segment; it is extremely convex anteriorly, and the point of articulation of the uropoda is upon the dorsal surface, though near to the lateral margin; behind the articulation of their appendages, the abdominal shield is flattened and terminates in a truncated, slightly concave extremity. The antennules have a four-jointed peduncle, the third joint being the longest, and a multiarticulate flagellum longer than the peduncle. The mandibles havea palp. ‘The first pair of thoracic appendages are shorter than the rest and subcheliform; the remaining thoracic appendages are very long, owing to the elongation of the fourth and fifth joints; they terminate in a single claw ; these appendages are covered with slender unbranched spines, which arise from tubercles. The uropoda are defective, but appear to have been larger than those of Munna, &c., and possibly more fully developed. Station 168; 1100 fathoms. Station 169; 700 fathoms. Fam. ASELLID &, Genus STeNETRIUM, Haswell. 1, STENETRIUM HASWELLI, 0. sp. A single species of this genus, the only known deep-water species, was dredged off the coast of S. America in 600 fathoms. ‘The specimen is a male, and measures 16 millim. in length. The diameter of the body is everywhere much the same except the head and the terminal region of the abdominal shield. The head is prolonged into a short rostrum; eyes are present of narrow linear shape, and set obliquely. ‘The thoracic segments are subequal in length as well as breadth, and the dorsal surface is quite smooth ; the margins of the first thoracic segment are prolonged into a triangular spiny process ; in the second segment the margin is furnished with a smaller spine-like process; in the two following segments there is in addition a smaller posterior spine; in the fifth segment the antero-lateral spine is much wider, occupying nearly the whole of the lateral margin; in the two remaining segments, the lateral 104 MR. F. E. BEDDARD ON ISOPODA COLLECTED [ Feb. 2, region is straight. The epimera are fused with the tergum in the first thoracic segment, elsewhere distinct but small. The abdominal shield is as long as the three last segments of the thorax ; it is subquadrangular in outline. The antennules have four basal joints and a long flagellum, longer than the peduncle. ‘The antenne are furnished with a rudimentary exopodite. The mandibles have a palp. The first pair of thoracic limbs are extremely long and prehensile ; the remaining thoracic limbs are slender and short, they terminate in twoclaws. The wropoda are biramose, the endopodite and exopodite being equal. Station 320; 600 fathoms. IOLANTHE, nov. gen. This genus appears to be closely allied to Acanthoniscus, Sars, with which it agrees in the absence of eyes and in the presence of long spiny epimera and long dorsal spines, and in the shape of the uropoda. It differs in that the thoracic appendages are biunguiculate and in a number of other points, which may be gathered from the following description of the single species referable to the genus. 1. IoLANTHE ACANTHONOTUS, 0. sp. This species is founded on a single female dredged in deep water in the Antarctic Ocean. It measures 24 millim. in length. The head is as wide as the succeeding segment of the thorax ; its margins are prolonged on either side into two spines, of which the anterior is much the longest; the anterior margin of the head is produced into a long rostral spine, which is curved slightly upwards. There is no trace of eyes. The thoracic segments are subequal in antero-posterior diameter; in the dorsal-median line of all the segments is a stout long vertical spine ; the lateral margin of the first segment is furnished with a long spiny process; on each of the three succeeding segments are two such spines, the anterior being the longer; in the remaining segments only the anterior spine is present. These spines are not outgrowths of the epimera, which are small and lie beneath them. The abdominal shield is almost circular in form ; on either side are three spines arranged at equal distances, which are much shorter than the lateral spines of the thorax. The antennules have a four-jointed peduncle, of which the second joint is the longest. The flagellum consists of 24 joints, and is about as long as the three distal joints of the peduncle. The antenne are half the length of the body ; the second joint of the peduncle has a spiny process on the outer side as in Janthe, which corresponds (?) to the exopodite ; the flagellum is nearly as long-as the peduncle. The mandibles have a palp. The thoracic appendages are all similar to each other and terminate in two claws. The wropoda have a very long proximal joint ; the endepodite is extremely short, though larger than the minute exopodite. Station 153; 1675 fathoms. ~ 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER. 105 Genus Jantra, Leach. 1, JANIRA ABYSSICOLA, N. sp. The present species is represented by a single female example, dredged off Fiji in very deep water. The head has a rounded anterior margin ; the eyes are completely absent. The first three segments of the thorax are of about equal length ; the next two segments are much shorter, being about one half the length of the anterior segments; the sixth segment has an antero-posterior diameter about equal to that of either of the anterior segments, while the seventh segment is longer than any. The antenne are longer than the body of the animal; the flagellum is much longer than the peduncle. The mandibles have a palp. The thoracic limbs are all similar to one another. The uropoda are as long as the abdominal shield ; they are biramose; the endopodite is stouter and longer than the exopodite. Station, 1350 fathoms. 2. JANIRA TRISTANT, N. sp. The head is broader than long, with very large, laterally placed eyes ; it is prolonged into a long stout rostrum with a rounded extremity. The first two segments are of about equal length; the three succeeding segments progressively diminish in length; the last two are again somewhat longer. The abdominal shield is sub- pentagonal and terminates in ashort blunt process. The antennules have a long flagellum ; the peduncle is composed of four joints, all of which are short. The mandible has a three-jointed palp. The thoracic appendages are all similar to each other. Off Tristan da Cunha, 100-150 fathoms. Genus Ja@ropsis, Kohler. 1. J@ROPSIS MARIONIS, N. sp. The only previously known species of this genus was described by M. Kohler, from the island of Sark; the present species was dredged off Marion Island in 100 fathoms. The single specimen measures 4 millim. in length. The head is roughly quadrangular in outline ; the anterior margin is prolonged between the antenne into a rostrum, which is deeply notched at the extremity; the eyes are of fair size, and dorsal in position ; the lateral margins of the head are-serrated. The head is about as long as the first two segments of the thorax taken together ; the latter are subequal, the third is slightly shorter, the fourth and fifth subequal and very much shorter again; the last two segments are quite as long as the two first ; the segments are separated by deep lateral incisions; the lateral margins of the segments are feebly serrated. The abdominal shield is somewhat triangular in outline, and terminates posteriorly in a three-jointed process; in the two notches separating these processes lie the uropoda; the Jateral margins are serrate. ‘The antennules are very short; the flagellum 106 MR. F. E. BEDDARD ON ISOPODA COLLECTED [ Feb. 2, has two joints, the distal one being very minute. The antenne have a five-jointed peduncle and four- or five-jointed flagellum ; the third joint of the peduncle is longer than the two basal joints, the fourth joint is shorter than the third, the fifth longer. The thoracic appendages are all similar and biunguiculate. Off Marion Island, 100 fathoms. Genus TRICHOPLEON, nov. gen. A single specimen of a deep-sea Isopod dredged at Station 215 does not fall very conveniently within any known genus of the Asellide. The general shape of the body is like that of Asellus, with which it also agrees in the uniunguiculate thoracic appendages ; eyes are completely absent ; the first four thoracic segments are furnished on either side with a forwardly-directed lateral spine. The antenne have a movable scale attached to the second joint, as in Janira and Stenetrium. The surface of the body is quite smooth. 1. TRICHOPLEON RAMOSUM, 0. Sp. The specimen is an immature female, measuring 5 millim. in length. The head is narrower, but longer than the succeeding segment of the thorax; it is prolonged into a short wide process anteriorly. There is no trace of eyes. The three first segments of the thorax are subequal in length; the fourth segment is shorter; the three posterior seginents gradually increase in length but diminish in breadth ; the antero-lateral margin of the first four segments is furnished with a short, acute, forwardly-directed spine. The abdomi- nal shield is oval, but wider anteriorly than posteriorly ; it terminates behind in the middle line in a short spiny process. The antennules are about as long as the head and first two segments of the thorax together ; the peduncle has four joints, of which the second joint is the longest; the flagellum consists of about fifteen joints. The antenne are about equal in length to the bedy; the flagellum is longer than the peduncle ; the two basal joints of the peduncle are very short, the third a trifle longer, with an articulated scale on the outer side ; the two distal joints are long and subequal. The mandi- bles havea palp. The thoracic appendages are similar to each other, terminating in a single claw. Uropoda moderately long, biramose, each ramus one-jointed. Station 214; 500 fathoms. Fam. ARCTURID&, Genus Arcturus, Latreille. 1. ARCTURUS MYOPS, N. sp. The present species differs from any other Arcturus at present known by the fact that the eyes are entirely or almost entirely aborted. The only trace of eyes left are a pair of rounded tubercles, which appear to contain no pigment and are not faceted. The largest 1886.] DURING THE VOYAGE OF H.M.S, ‘CHALLENGER.’ 107 individual measures about 9 millim. The first four thoracic segments are subequal in length ; each is ridged posteriorly, the ridge widening out laterally to occupy the whole of the segment, it is covered with fine granulations ; in the fourth segment the ridge is higher than in the preceding segments; auteriorly between the ridge and the anterior margin of the segment is a shorter ridge, likewise covered with numerous minute tubercles ; on the first thoracic segment is a third ridge; of the three posterior segments the first is the longest ; on each is a posterior ridge-like elevation beset with numerous tubercles. The abdominal shield is oval, tapering towards its extremity, which is slightly upturned; like the thorax, it is tuberculate. The proximal joints of the antennze and of all the thoracic limbs are beset with tubercles. Station 169; 700 fathoms. 2. ARCTURUS ANNA, 0. sp. This single specimen of this large species measures 37 millim. ; the antenne are nearly twice the length of the body. The head is excavated in front ; the antero-lateral margin of the head is notched ventrally. The first four segments of the thorax are subequal ; each is traversed by a ridge, which dorsally is narrow and only occupies the posterior portion of the segment, laterally it is widened out and occupies the whole of the segment ; in front is another shorter ridge, which does not reach the lateral region of the segment ; at the extreme lateral margin is a stout spine, inclined nearly at right angles to the longitudinal axis, which overlies the epimeron; behind are one or two shorter spines along the postero-lateral border of the tergum. The epimera, which are short, are likewise furnished with one or two short spines ; these are only conspicuously developed upon the last two of the segments, especially upon the last, where one of the spines equals in length the tergal spine which it directly underlies. Of the three posterior segments the first is decidedly the largest ; they are ridged like the anterior segments, the ridge widening out laterally ; each segment has a short lateral spine corresponding to those on the anterior segments ; the epimera are also furnished with a stout spine, that of the fifth segment with an additional spine directed forwards. There are two completely free abdominal segments, the third being to a large extent fused with the abdominal shield; on the ventral side of the first abdominal segment is a short spine on either side anteriorly and another pair of longer spines posteriorly ; this segment as well as the next has a short lateral spine; the third abdominal segment has on either side a long curved spine at the postero-lateral margin. The abdominal shield has a central convexity occupying nearly the whole of its extent and bordered by a flattened rim, which is serrated, and terminates posteriorly in a pair of pointed processes projecting behind the central area, which terminates posteriorly ina short pointed spine. The thoracic limbs of the second, third, and fourth pairs have one or two longish spines on the three proximal joints. Station 320; 600 fathoms. 108 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, 3. ARCTURUS CORNUTUS, 0. sp. This species, like the last, is represented by a single female ex- ample, measuring 36 millim. ; the length of the antennz is 64 millim. The margin of the head is excavated dorsally and anteriorly ; the antero-lateral margin of the head below and in front of the eyes is notched ; between the eyes are a pair of long, forwardly-directed spines, and behind the eyes a pair of blunt tubercles. The first three thoracic segments are subequal, and each is a little longer than the fourth. Each of the segments is ridged as in the last species ; the lateral margin of the tergum has a long spine in each of their segments, and there is another spine of equal length placed halfway between the dorsal median line and the lateral margin of the seg- ment; on the fourth segment there is an additional lateral spine placed behind the principal spine; there are indications of a corre- sponding spine in the anterior segments. The epimera of segments 2-4 have a single spine near to their posterior margin, the lengths of which increase progressively from before backwards ; in front of the posterior tergal ridge are a pair of blunt tubercles united by a slight elevation ; the first segment has also a single tubercle placed in front of this. Each of the three posterior segments is ridged as in A. anna ; laterally is a long spine which overlies a similar spine upon the epimeron ; the first of these segments has also a somewhat longer epimeral spine directed forwards. Each of the three free abdominal segments has along lateral spine ; the first segment has ventral spines as in the last species. The abdominal shield has the same shape as in A. anna, but there is a distinct longitudinal keel terminating in a sharp upturned point ; on either side is a single row of curved hook- like spines. The 2nd, 3rd, and 4th pairs of thoracic limbs have spines similar to those of the last species. Station 214; 500 fathoms. 4. ARCTURUS BRUNNEUS, N. sp. This species measures 19 millim. in length, the antenne being of about the same length. The head is furnished with a pair of long spines between the eyes, and a pair of shorter spines behind these, which are, however, longer in the female. The first four thoracic segments are subequal, ridged as in the last two species ; on this ridge are implanted a number of long, straight, slender spines. In the male the first segment has four equidistant spines and a minute epimeral spine at the extreme lateral margin; on the second segment the epimeral spine is longer, and there is a minute tubercle between it and the lateral tergal spine; in the third and fourth seg- ments the lateral tubercle is developed into.a spine, and there is also a short median dorsal spine ; on the second, third, and fourth seg- ments there is a transverse row of longish spines near to the anterior margin of the segment in both sexes; in the female the spines are longer. Each of the three posterior thoracic segments bears a ridge, with a single row of long spines arranged at equidistant intervals ; there are three pairs of these spines, one pair epimeral; in the 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 109 female there are several shorter ones in addition. The first abdo- minal segment has a single row of comparatively short backwardly- directed spines ; on the second and third segments these spines get to be considerably longer, especially the lateral spine on either side, which marks the commencement of the abdominal shield. The abdominal shield in both sexes is covered with longish curved spines ; just above and near to the termination of its lateral margins are an extremely long pair of spines directed outwards and slightly upwards. ‘The proximal joints of the antenne and of the thoracic appendages are furnished with spines. The uropoda are tuberculate in the male and spiny in the female. Station 147 ; 1600 fathoms. 5. ARCTURUS PURPUREUS, l. sp. This species is represented by a single female, which is of a purplish colour, It measures 18 millim., the length of the antennee is 31 millim. On the head between the eyes are a pair of long forwardly curved spines; the hinder portion of the head is occupied by a rounded median convexity; on the antero-lateral margin is a very short forwardly directed spine, beneath which the margin is excavated by a semicircular notch. Of the first four thoracic segments, the fourth is rather the shortest; each of the segments bears an outwardly directed spine on each side of the body, corresponding in position to those upon the head; close to the lateral margin of each segment and projecting over the epimeron is another long spine; the first segment differs from the succeeding in having no free epimera, and the lateral margin has two spines instead of one, of which the anterior is the longer; the fourth segment has also a second spine at its postero-lateral margin. Of the three posterior thoracic seg- ments the first is the largest; the epimera of all have a long out- wardly directed spine ; the first of these segments has in addition a tergal spine on either side exactly overlying the epimeral spine. The first abdominal segment has a pair of long lateral spines and a pair of short ventral spines; the third segment has a pair of lateral spines. The abdominal shield is oval, with a faintly marked central keel, terminating posteriorly in a long spine; its lateral margins are flattened and unite posteriorly ; on either side are two flattened spines situated at equidistant intervals. The antennz and anterior thoracic limbs have a few spines upon the proximal joints; the uropoda are granulated, but bear no spines. Station 23; 450 fathoms. 6. ARCTURUS SPINIFRONS, 0. sp. This species reaches to a length of 13 millim., the antenne measuring 20 millim. The body is extremely tuberculate, but there are no spines except a single pair upon the head ; the lateral margin of the head, as in A. anna, is notched ventrally. The four anterior thoracic segments are subequal, each has a posterior ridge which 110 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, widens out laterally ; the ridge is concave forwards, dorsally, and closely embraces a median oval convexity which lies in front of it ; the fourth thoracic segment has a row of short tubercles, arranged in a semicircle with the concavity directed forward, on the ventral surface. Of the three posterior thoracic segments the first is the largest, the second and third being smaller and subequal; each of the segments is traversed dorsally by a strong ridge, which is tuber- culate ; the first of these segments has a number of short tubercles scattered over the ventral surface, and the two succeeding segments are ridged in the same region. The segments of the abdomen are comparatively smooth, being only slightly roughened laterally. The abdominal shield is smooth with the exception of the lateral margins, which are serrate ; it terminates in a short median spine. The thoracic appendages are tuberculate on the proximal joints ; the uropoda bear a single median longitudinal row of tubercles. Station 174; 600 fathoms. 7. ARCTURUS SPINOSUS, N. sp. This is the largest of the deep-sea species, measuring up to 48 millim., the antenne measure 60 millim. The males differ slightly from the females, the latter being wider in the thoracic region and more spiny. The anterior margin of the head is exeavated ; between and a little in front of the eyes are a pair of long spines, behind these are a pair of shorter spines; in the female there is an additional pair of spines situated outside these latter. Of the first four thoracic segments, the fourth is slightly the longest in the male; in the female all four are subequal. On the first three thoracic seg- ments, the posterior ridge bears three pairs of long spines situated at equidistant intervals; the fourth thoracic segment has only two pairs, but the epimera have each a long spine, wanting in the anterior segments. In the female the first thoracic segment has four pairs of spines, the other segments being as in the male; between these principal spines there are, however (in the female), numerous smaller spines, and the margins of the epimera are furnished with short spines; each of these segments has in both sexes an anterior ridge covered in the male with blunt tubercles, in the female these tuber- cles are pointed. Of the three posterior thoracic segments the first is the longest ; the posterior ridge is tuberculate, the tubercles being more strongly marked in the female ; the epimera of these segments have a large lateral spine. The three first abdominal segments are distinct ; the last free segment has a long lateral spine on either side in the female. The abdominal shield terminates in a single median spine, and in two longer upwardly curved lateral spines. The surface of the abdominal shield is tuberculate in the male and covered with short spines in the female ; in this sex there are in addi- tion a pair of moderately long lateral spines, situated just in front of the posterior lateral spine. The thoracic appendages in the female have a few short spines; in the male only the three last pairs are thus provided ; the uropoda are tuberculate. Station 146; 1375 fathoms. 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 111 8. ARCTURUS GLACIALIS, n. sp. This new species comes near to the last, but may readily be distinguished by the fact that the spines are more numerous, shorter, and more slender. The single example, a female, measures 32 millim. The dorsal surface is densely covered with short slender spines, which extend on to the thoracic appendages and uropoda; the spines are of uniform length. The anterior margin of the head is excavated by a shallow semicircular notch ; between and in front of the eyes are a pair of long spines, inclined somewhat away from each other ; the spines on the thoracic segments are disposed in the following way :—each of the first four segments has a posterior and anterior ridge as in other species; both these are covered with spines, as are also the epimera; between the two ridges in all but the first segment are a pair of short spines; each of the three posterior thoracic segments is ridged, the ridge being beset with spines except in the median dorsal line. The abdominal shield is beset with spines, except in the dorsal median line, where it is grooved longitudinally. Station 153; 1675 fathoms. 9. ARCTURUS ABYSSICOLA, 0. Sp. This species was obtained from two stations in the Pacific Ocean, but near to each other. The length is about 20 millim., the length of the antenne 42 millim. Of the first four thoracic segments the second and third are equal in size and rather longer than the first and fourth; each of these segments is ridged posteriorly as in other species ; laterally the tergum is produced into a short tubercle and there is a similar tubercle upon the epimera; on the first segment this tubercle is prolonged into a spine ; on the inferior surface of the fifth segment is a short median transverse ridge ; the first abdominal segment has a pair of ventral tubercles ; the abdominal shield is keeled and terminates in a blunt spine, it is covered with a few low scattered tubercles. The anterior thoracic appendages are furnished with one or two spines upon the proximal joints; as in 4. anna the posterior thoracic appendages have not these spines. Station 184; 1400 fathoms. Station 281 ; 2385 fathoms. 10. ARCTURUS STUDERI, N. sp. The extreme length of this species is 28 millim., length of antenne 30 millim. The head has two pairs of long spines situated one behind the other, behind these again is a ridge bearing a few short spines ; the antero-lateral region of the head is notched ventrally as in A. purpureus, &c. The four anterior thoracic segments are subequal ; on the posterior ridge of the first Segment are a pair of minute tubercles on either side of the median dorsal line; laterally are two long spines equidistant from each other and the dorsal tubercles ; the lateral margin of the tergum is prolonged into two outwardly directed spinous processes ; in front of the posterior ridge are four minute tubercles arranged transversely ; the second segment 112 MR, F. E. BEDDARD ON ISOPODA COLLECTED [ Feb. 2; is similar ; the third and fourth segments have in addition another spine upon each side, placed between and behind the two lateral spines ; the margins of the epimera are prolonged into three short spines. Each of the three posterior thoracic segments has two or three long spines on either side; the epimera are large and terminate in two stout spines. The two anterior abdominal segments each consist of two portions—a narrower anterior and a smaller posterior portion ; the former is smooth, the latter beset with spines and tubercles ; on the first segment are two particularly long spines, one situated close to the ventral margin of the tergum, exactly above this is the other, which is of equal length; on the second segment is a lateral spine of great length, but situated more dorsally ; the third segment has also a pair of lateral spines. The abdominal shield has a dorsal keel which is prolonged posteriorly into a curved spine. The whole of the dorsal surface is covered with minute pointed tubercles; the lateral region of the abdominal shield is flattened as in A. anna, &c., and terminates posteriorly on either side in a flattened triangular spine. Kerguelen, Royal Sound ; 28 fathoms. ' 11. ARCTURUS OCULATUS, 0. sp. Five specimens of this small species were dredged in shallow water off Melbourne, South Australia. The largest measures no more than 7 millim. The most remarkable point about this species, and one which serves at a glance to distinguish it from any other recorded species of the genus, is the elevation of the eyes on to stalks as in the genus Munna. The frontal margin of the head is broad and truncated ; it is not excavated as in so many other species. The first four thoracic segments are subequal in length, they are convex posteriorly and flatter anteriorly ; the surface of these segments is quite smooth and free from tubercles or spines ; in the last three of these segments the epimera are furnished with a long spine. The posterior thoracic segments, like the anterior, possess an epimeral spine ; each of these segments has also a lateral tergal spine. Of the three tree abdominal segments the first and third are furnished with a lateral spine on either side, which is absent from the middle segment. ‘The abdominal shield is very convex, and terminates in a median dorsal spine as in so many other species ; the lateral margin of the caudal shield is beset with a series of somewhat curved spines situated at equidistant intervals, the lateral margin terminates in a longish flattened spine as in A. anna. On either side of the dorsal median line is another row of spines, which run from end to end of the caudal shield. Station 161 ; 38 fathoms. Family CyMorHoOIpDs#, ANUROPUS, Rov. gen. Among the Isopoda dredged during the cruise of the ‘ Challenger,’ there are not many deep-sea species which present any striking differences from the Isopoda of shallow water. One of these species 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 113 is represented by a single specimen, which was dredged in the Pacific Ocean at Station 218, in 1070 fathoms of water. It isa large Isopod, measuring upwards of two inches in length, and agrees in most particulars with such genera of the Cymothoide as Aga; but at the same time it presents certain remarkable peculiarities analo- gous to those exhibited by the aberrant genus Bathynomus lately described by Prof. A. Milne-Edwards from deep water in the North Atlantic. M. Milne-Edwards’s preliminary account of Bathynomus was communicated to the French Academy’, and a translation of his note has appeared in the Ann. & Mag. of Nat. Hist.? Apart from its huge size, the most remarkable feature in the organization of Bathynomus is the great development of branchial organs : ‘‘ it appears,” says M. Milne-Edwards, ‘‘ that the respiratory apparatus of an ordinary Isopod is insufficient to supply the physio- logical needs of Bathynomus, and that the development of special organs of a greater functional power has been rendered necessary. The abdominal limbs, which usually in this group constitute the sole branchial apparatus, in Bathynomus only serve the function of a covering to the gills which lie beneath them.” The gills of this Crustacean are in fact represented by a series of complicated branched outgrowths of the body-wall in the ventral region of the abdomen. The same end is attained by the Crustacean, which forms the sub- ject of the present remarks, in a different manner. Instead of a development of accessory respiratory organs, Anwropus (as I may term the genus from its chief structural peculiarity) exemplifies one extreme of the Isopodan type, in that all the abdominal appendages are converted into respiratory organs; the increase of respiratory surface is thus attained by an exaggeration of a structural character, which is common to all the members of the family, and which indeed is an important basis of distinction from other families of Crustacea. In all the members of this group more or fewer of the abdominal limbs are soft foliaceous appendages, which permit of an easy exchange of gases between the contained blood and the sea-water. There is no instance, however, among the Isopoda in which all the abdominal appendages are similar, functioning as respiratory organs, except in this deep-sea genus Anuropus. Bathynomus, as regards the uropoda, is quite a typical Isopod; these appendages form a pair of swimming-feet as they do in the other Cymothoide ®*. The modifications of the terminal pair of abdominal appendages or uropoda serve to divide the Isopoda into natural families, which prove to be allied in other particulars ; and some stress, therefore, from a classificatory point of view, should perhaps be laid upon the fact of their modification in Anuropus, though it is always open to question how far a purely adaptive character is of value. Since the present genus agrees with the Cymothoide in the general form of the body, in the number of free abdominal segments, and in fact in all essentials, it would perhaps be hardly permissible to remove it 1 ‘Comptes Rendus,’ Jan. 1879. ? Ann. & Mag. Nat. Hist. 1879 (vol. iii.), p. 241.. ® There is a figure of Bathynomus in an interesting work recently published by M. Filbol and entitled ‘La vie au fond des mers,’ Paris, 1885. Proc. Zoou. Soc.—1886, No. VIII. 114 MR. F. E. BEDDARD ON ISOPODA COLLECTED __[ Feb. 2, from that family on account of the branchiate uropoda; but Anuropus should at least be regarded as the type of a special subfamily equivalent to any of the other four, viz. Cymothoadiens errants, C. raviseurs, C. branchiferes, and C. parasites, into which MM. H. and A. Milne-Edwards have divided the family. Anuropus has a further ‘‘abyssal character” in the absence of eyes, and it is also remarkable for the abortive antennules, which are only repre- sented by two joints—a stout basal joint, and a longer stout curved distal joint, which is possibly the equivalent of a metamorphosed flagellum. The single species I may term 1, ANUROPUS BRANCHIATUS, 0. sp. The extreme length of the specimen, which is a female, is 70 millim. The head is small, and entirely without eyes; the body is extremely convex ; the thoracic segments are subequal, the six posterior are furnished with distinct epimera; the abdominal segments are all smaller than the thoracic segments and subequal ; the fifth segment is fused with the telson and forms a caudal shield, which is rounded and flattened in shape. ‘There is no trace of eyes; the antennules are short and thick, consisting of a thick basal joint and a longer, some- what curved distal joint. The antenne are longer and more slender, and quite normal in structure; the mandibles have a three-jointed palp. The abdominal appendages are all similar to each other, consisting of a short, stout, basal joint, and two equal rami flattened and rounded in form. Station 218; 1070 fathoms. Fam. SPH ZROMIDS. Genus Cymopocea, Leach. 1, CYMODOCEA ABYSSORUM, 0. sp. This species is the only representative of the family at present known from deep water ; it is represented by two individuals, one a male, the other a female. The body in both is flattened, and is evidently incapable of being rolled into a ball. The eyes are small and whitish from the absence of pigment ; the first thoracic segment is broader than the head, the following segments are subequal, and with well-acveloped sickle-shaped epimera, absent in the last of the seg- ments. Abdominal shield with two bluat conical spines on the dorsal surface, one behind theother ; posterior extremity obtuse and rounded. Uropoda with the rami subequal in the female, the outer being slightly the longer; in the male the outer ramus is very much longer than the inner and curved inwards. Station 218 ; 1070 fathoms. Fam. APSEUDID2&. Genus ApseupEs, Leach. 1. APSEUDES ANTARCTICA, 0. sp. The largest specimen of this small species measures 4 millim. in length. The cephalothorax is nearly as long as the first four segments 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 115 of the thorax ; it terminates in the middle line anteriorly in a sharp rostral prolongation. The free thoracic segments increase in length, but decrease in width up to the fourth, but there is less difference between the first three than between the third and fourth; the fourth and fifth segments are subequal ; the sixth is shorter, but not perceptibly narrower than the fifth ; in the first segment the epimera are prolonged into a spine; on the fourth and fifth segments are two knob-like projections on either side, equidistant from each other, and from the epimeron; on the terminal segment there is a single process; the five anterior abdominal segments are subequal, and furnished laterally with sharp spiny epimera. The caudal shield is hourglass-shaped, being constricted in the middle, it narrows rapidly to the obtusely pointed extremity. The outer flagellum of the antennules has eight joints, the inner only three. ‘The uropoda are extremely elongated ; the endopodite has two joints, the exopodite six. Kerguelen ; 120 fathoms. TYPHLAPSEUDES, nov. gen. This genus is distinguished from Apseudes by the almost complete disappearance of the ocular lobes, which are represented by a small triangular process without any trace of ocular structures; by the absence of an exopodite to the chelipeds and fossorial limbs; and by the fact that the exopodite of the abdominal appendage is distinctly bi- articulate. In the last character this genus agrees with Sphyrapus. 1. TyPHLAPSEUDES NEREUS, 0. Sp. This species attains to a length of about 10 millim. The body is somewhat flattened and depressed, very much wider anteriorly than posteriorly ; the cephalothorax terminates in front in a sharp rostrum; to the outside of the antennules is the triangular pointed ocular lobe, which contains no optic structures; some way below this is a pointed lateral process. The free thoracic segments diminish in breadth, but increase in length up to the fifth; the sixth is narrower but shorter than the fifth; the epimera of the first thoracic segment project as a spiny process; the lateral margins of all but the first two segments are furnished with a short spine placed halfway between the epimera and the anterior margin of the segment ; on the ventral median line of the thoracic segments is a spiny process ; similar minute spines exist upon the abdominal segments. The abdominal segments with the exception of the last are furnished with small pointed epimera; the last segment is as long as four of the anterior segments, it terminates in a straight truncated extremity, in the middle of which is a short knob-like process. The antenne have a rudimentary exopodite. The chelipeds and fossorial limbs are normal in structure, but possess no exopodite. The uropoda are extremely long, as in Apseudes. Station 23; 450 fathoms. 8? 116 MR. F. E. BEDDARD ON ISOPODA COLLECTED _[Feb. 2, LEIOPUS, nov. gen. This genus is closely allied to the last, but differs in that the chelipeds and fossorial limbs have an exopodite. The chelipeds are extremely slender and delicate in their structure, and this, together with the characters of the abdominal appendages, serves to distinguish the genus from Apseudes. 1. LEIOPUS LEPTODACTYLUS, 2. sp. This species attains to a length of 13 millim. The cephalothorax is prolonged in front into a long rostrum ; the ocular lobes are large and pointed anteriorly ; there is no trace of any optic structures; behind the ocular lobes are two long spiny processes, one on either side. The first free segment of the thorax is as wide as the cephalothorax; the following segments decrease in width, the first suddenly, the rest more gradually; the length of these segments increases up to the fourth; the fifth is of equal length with the fourth, the sixth rather shorter ; the first segment has well-developed spiny epimera; the last three segments of the thorax have also short spines upon the epimera, which are wanting in the intermediate segments; upon all the free thoracic segments, with the exception of the first, are a pair of long lateral spines like those of Typhlapseudes, but longer. On the ventral surface of both the thoracic and abdominal segments, with the exception of the last, is a median spine. The abdomen is much as in the last-described species. The outer flagellum of the antennules has twenty-seven joints, the inner only six. The antenne have a rudimentary exopodite. The chelipeds are very slender and delicate. The uropoda are as in Apseudes. Station 78; 1000 fathoms. Fam. TANAIDS. Genus Tanaris, Audouin & Milne-Edwards. 1. TANAIS HIRSUTUS, D. sp. The extreme length of this species is 9 millim. The body is elongated, the anterior region is wider than that which follows; the last thoracic segment and the first three abdominal segments are again wider, after which the body narrows towards the termination. The cephalothorax has a short obtuse rostrum; the two first segments of the thorax are short and subequal, the third segment is narrower but longer; the two following segments increase progressively in length, the first is about twice the length of the preceding segment; the last thoracic segment is wider than the preceding, but shorter. The first three segments of the abdomen are wider as well as longer than the following ; the terminal segment ends in a blunt, rounded extremity. The antennules have a three- jointed peduncle anda two- or three-jointed palp ; the extremities of the joints of the peduncle are surrounded by a circle of fine delicate plumose hairs of great length. The antenne are similarly beset 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 117 with fine hairs. The uropoda are uniramous and consist of twelve joints. Off Prince Edward’s Island ; 50-150 fathoms. Genus TypaHiotanats, G. O. Sars. 1. TYPHLOTANAIS KERGUELENENSIS, 0. sp. The individuals of this species measure up to 3 millim. in length. The cephalothorax is short and wide; it is prolonged between the antennz into a short pointed triangular process ; eyes completely aborted. The first segment of the thorax is shorter than the rest which are subequal, diminishing slightly towards the posterior extremity of the body ; the first segment has a compressed forwardly- directed spine arising from the median ventral surface ; there is a trace of a similar process on the second segment. The first pair of thoracic appendages arise close to the anterior border of their segment, the second pair further back, the third pair from about the middle of the segment; the three posterior pairs of thoracic appendages arise close to the posterior boundary of their segments. The antennules are about as long as the cephalothorax. The chelipeds are rather slender. The wropoda are biramose, the outer ramus one-jointed, the inner two-jointed. Kerguelen, Christmas Harbour ; 120 fathoms. 2. TYPHLOTANAIS BRACHYURUS, 0. sp. The length of this species is 8 millim. The cephalothorax is hardly longer than the first free thoracic segment; the first thoracic segment is one third less than either of the two following, which are sub- equal; the fourth segment is hardly shorter than the third, the fifth and sixth decrease progressively. The first pair of appendages is attached close to the anterior border of the segment; the two following pairs are moved a little way back, but are still quite close to the anterior extremity of their segments; the three posterior pairs are attached close to the posterior border of their segments. There is no ventral spine on the first free segment. The abdomen is short, and not so long as the last two segments of the thorax. The antennules are rather shorter than the cephalothorax. The chelipeds are short and stout. As in the last species, the three following pairs of appendages are more slender than the three posterior pairs. The uropoda are as in the last species. Station 246 ; 2050 fathoms. NEOTANAIS, noy. gen. This genus comes nearest to Heterotanais, but differs in the great length of the endopodite of the uropoda, and in the fact that the chel are fully developed and of the normal structure in the male ; a well-marked character of this genus is the specialization of the thoracic appendages into an anterior and posterior series; in the first three pairs the distal joint of the limbis a single, somewhat curved 118 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, claw ; in the posterior appendages this terminal joint is furnished at its distal extremity with a circlet of slender spines and a long, mesial, slender hair. 1. NEOTANAIS AMERICANUS, N. Sp. The species is represented by two specimens, both males, mea- suring about 7 millim. The body is elongated and everywhere of approximately the same diameter. The cephalothorax has a convex anterior margin ; on either side of the antennules are the minute, but separate, ocular lobes, which, however, show no traces of ocular structures. The thoracic segments increase in length up to the fourth, after which they diminish. The five anterior abdominal segments are subequal, the terminal segment is of course longer, it terminates in a minute, median, triangular process. The antennules consist of a three-jointed peduncle, and a four-jointed flagellum, the joints of which are very minute. In the antenne the peduncle is tive-jointed, and the flagellum consists of four joints. The chelipeds are short and stout. ‘There is no difference in size between any of the succeeding thoracic appendages, only the difference in the terminal joint referred to above. All the abdominal appendages are present ; the wropoda consist of a very stout basal joint, with which are articulated the long eight-jointed endopodite and the small two- jointed exopodite. Station 45; 1250 fathoms. Station 323; 1900 fathoms. Genus LerroGnatuiA, G. O. Sars. 1, LeproGNATHIA AUSTRALIS, 0. sp. A single female example of this species was dredged in shallow water at Kerguelen, it measures 4 millim. The body is extremely narrow and elongated. The cephalothorax is longer than the first segment of the thorax, but not so long as the first two segments ; the eyes are completely absent ; the first segment of the thorax is shorter than any of the three following, which are subequal, and each about half as long again as the first segment; the fifth segment is shorter than the fourth, but a trifle longer than the first; the last segment of the thorax equals the first in length; the first pair of thoracic appendages are articulated close to the anterior margin of their segment ; the second, third, and fourth pairs at about the middle of their respective segments ; the last two pairs are articulated a very little nearer to the posterior margin. The abdomen is altogether as long as the last two segments of the thorax and one half of the fourth. The antennules are not so long as the cephalo- thorax, they are four-jointed. The chelipeds are stout and robust, all the joints are smooth, the distal joints are not serrated as in L. longiremis, the three anterior pairs of thoracic appendages are more slender than the posterior pairs. The rami of the uropoda are both biarticulate, but the endopodite is much longer and stouter than the exopodite. Kerguelen, Christmas Harbour, 120 fathoms. 1886.] DURING THE VOYAGE OF H.M.S. ‘CHALLENGER.’ 119 Genus Pararanats, Dana. 1. PARATANAIS BATHYBROTIS, 0. sp. The single specimen measures 4 millim. The cephalothoracic shield is about as long as the following two segments of the thorax ; it is prolonged anteriorly into a wide obtusely pointed rostrum. Eyes are present and well developed. The first segment of the thorax is rather shorter than the rest, which are subequal. The length of the abdomen is about one fourth of that of the entire body. The antennules have a very characteristic form; they are composed of four joints ; the basal joint is as long as the rest of the appendage, and is extremely wide and flattened ; the following joint is short and wide ; the third joint is no longer, but is narrower ; the terminal joint, which represents the flagellum, is short and conical in form. The antenne are shorter than the autennules, but, like them, consist of four joints ; the first joint is wide and flattened, the second joint bas the same shape, but is shorter, the third joint is narrow and cylin- drical ; the distal joint is short and narrows towards its termination, Station 246; 2050 fathoms. 2. PARATANAIS DIMORPHUS, 0. sp. A very considerable number of individuals of a small species of Paratanais were dredged in shallow water at Kerguelen, which are to be distinguished by a very pronounced sexual dimorphism. The female is like many other species of the genus; but the male is remarkable on account of the more slender body and the great difference in the structure of the chelipeds. Both males and females measure, in most cases, 3 mm.in length. In the male the cephalo- thorax is rather long and narrow, and equals in length the first three segments of the body together with half of the fourth; the first free segment of the thorax is the shortest; the second is twice the length of the first; the third ‘segment is half as long again as the second ; the fourth and fifth are subequal and about half as long again as the third ; the last segment is about equal in length to the third. The abdomen equals in length the last two thoracic segments. The antennules consist of five joints; the antenne of six. In the female the antennary organs are shorter, the antennules being three- jointed and the antennze five. The chelipeds are long; both the moveable and the fixed ‘ finger’ are of great length; the latter is, however, not as in other Tanaids a mere prolongation of the penulti- mate joint, but is freely moveable, being articulated with it. In the female the chelipeds are quite normal in structure. The wropoda are biramose, each ramus being two-jointed. Kerguelen, Christmas Harbour, 120 fathoms. Fam. ANCEIDS. Genus Anceus (PraAn1za), Risso. 1. ANCEUS BATHYBIUS, D. sp. Only a single fragment of this species was obtained from deep- water ; the abdomen was entirely wanting. The specimen is a male 120 MR. F. E. BEDDARD ON ISOPODA COLLECTED [Feb. 2, and measures 10 millim. The head terminates anteriorly in a very long obtusely pointed rostrum. Eyes are completely absent. The first three segments of the thorax are, as usual, much shorter than the two following. The surface of the body is smooth. The first pair of thoracie appendages are operculiform and consist of five joints, the second being much the most important; the two following pairs of appendages differ from the two last in being very much more slender, otherwise their structure is much the same. Station 76; 900 fathoms. 2. ANCEUS GIGAS, N. sp. This large species is represented by a number of individuals both male and female; the largest specimens measure as much as 16 millim., the females being hardly smaller than the males. In the male the anterior margin of the head is almost straight, being only broken by three minute processes, one of which is median. The thoracic segments are quite like those of other species; the lateral regions of these segments are roughened, the dorsal smoother. The abdominal segments are furnished with well-developed sickle-shaped epimera, which instead of projecting outwards from the body are bent down. ‘The first thoracic appendages agree with those of the last species in having six joints; the remaining thoracic appendages are all similar to each other. Kerguelen, Christmas Harbour, 120 fathoms. 3. ANCEUS TUBERCULOSUS, N. sp. A second species of Anceus was obtained at Kerguelen, which cannot be confounded with the preceding; it is represented by a considerable number of specimens, both males and females. The largest male measures only 5 millim. in length. The head is pro- longed in the middle line into a short rostrum, which is squarish in outline and has a semicircular notch at its extremity. The dorsal surface of the head is very convex, and is covered with numerous tubercles, which are especially abundant posteriorly and laterally. The three anterior segments (including the rudimentary first free segment) are similarly beset with tubercles ; the remaining segments are smooth. The segments of the abdomen gradually increase in length, they are furnished with well-developed sickle-shaped epimera, which project outwards. The ambulatory limbs are all similar to each other; the five anterior abdominal appendages are flattened and smooth, without any hairs. Kerguelen, Christmas Harbour, 120 fathoms. Kerguelen, Royal Sound, 30 fathoms. 4, ANCEUS LATIDENS, n. sp. A single male specimen of this species measures 2°5mm. The anterior margin of the head is prolonged into three short, blunt pro- tuberances, of which the median one is the largest. The head and 1886.] DURING THE VOYAGE OF H.M.S. ‘ CHALLENGER.’ 121 the first four segments of the thorax are tuberculate, the two remain- ing segments and the rudimentary terminal segment being smooth. The abdominal appendages have epimera, which are directed down- wards as in A. gigas. The operculiform first pair of thoracic appendages are like those of the majority of species in consisting of a single large basal joint, a small second joint, and a minute rudi- mentary third joint. The remaining thoracic appendages are similar to each other; the proximal joints are stout and bent, with short stout spines. The abdominal appendages differ from those of the last species in that both rami are setose, the outer perhaps more so than the inner. Flinder’s Passage, North Australia, 7 fathoms. The forty-four species which have been briefly described in the foregoing pages do not include all the novelties in the ‘ Challenger’ collection; there are a few other species which I have not yet examined with sufficient care to report upon, but which, so far as I am aware at present, are undescribed forms. These include one species of Arcturus, one of the allied genus Astacilla; two species, one from deep water, the other from Kerguelen, which are represen- tatives of the genus Paranthura. The total number of new species of Isopoda obtained during the voyage of the ‘Challenger’ is therefore about 70, comprising 10 new genera. Geographical and Bathymetrical Distribution.—It is interesting to note that all the existing families of Isopoda without a single exception * are to be found in the deeper waters of the ocean; but the number of deep-sea species differs very considerably in the different families ; the most characteristic are evidently the Mun- nopsidze and Arcturidz, and, in a somewhat less degree, the Tanaids, Asellids, and Serolidze ; the occurrence of a single species each of the Anceide, Cymothoidee, Anthuride, and Spheeromide may perhaps be taken as an indication that these families are not largely represented in the deep-sea fauna. In most cases the deep-sea species are distinct from the shallow- water species ; only one or two (e. g. Arcturus furcatus, Studer) are known, which are common to shallow water and the great depths. In many eases the deep-sea genera are distinct, and this is particularly so in the Asellids ; of this group, Acanthoniscus, Sars, Acanthomunna, Trichopleon, Iolanthe, are absolutely confined to deep water, while Ischnosoma has four deep-sea species and only one which is an inhabitant of shallow water in the extreme north, where the con- ditions of temperature are much the same. Very frequently the deep-sea Isopoda are distinguished by the extremely spiny character of the body; this is largely the case with the deep-sea Arcturi, and there are other instances. The great development of spines upon the body is not, however, confined to the deep-sea Isopoda, but is also found in many species from the colder regions, at Kerguelen, * Sars has described a species of Idotheide, Glyptonotus megalurus, which enables me therefore to enunciate the general statement, 122 ON A VARIETY OF ANTHOCHARIS EUPHENO. [Feb. 2, and in the Arctic Ocean; it appears therefore to be correlated in some way which is not understood with a low temperature of the water. The majority of the deep-sea Isopoda are entirely blind, or have, at most, rudimentary eyes devoid of pigment ; of the deep-sea species obtained by the ‘ Challenger ’ only 25 p.c. have well-developed eyes, and all these species but three belong to the Arcturidz, which form avery striking exception to the general rule. In every instance but one the genera which are confined to the deeper waters are blind ; and it is just possible that the presence or absence of eyes may he an indication of the time which the species has inhabited the deep sea. It is commonly believed that the deep-sea species are larger than their shallow-water allies; the examination of the ‘ Challenger’ Isopoda lends some support to this view. Of the families Serolide, Munnopside, Areturide, Asellidee, and Munnide the deep-sea species are certainly the larger. With regard to the range in depth, the greatest depth at which any species has been met with is 2740 fathoms; the species obtained at this great depth is Hurycope intermedia. Only a few species descend below the 2000-fathom line, indeed only three to any extent. The majority of the deep-sea forms were dredged in the intermediate zone of 1000-2000 fathoms—twenty-three species out of a total of forty-four, and this does not include five species which were dredged just below the 1000-fathom limit, viz. in 1000-1070 fathoms. I hope to discuss more fully the distribution of the deep-sea Isopoda in my forthcoming Report. 5. On a Variety of Anthocharis eupheno, from Mogador. By J. H. Lescu, F.Z.S. [Received January 18, 1886.] During a recent excursion to Mogador I obtained examples of a new form of orange-tip Butterfly, which I propose to call ANTHOCHARIS EUPHENO, var. ANDROGYNE. The male of this variety differs from the typical A. eupheno in its larger size, and in the fainter markings of the underside of the hind wings, which are rarely strong enough to be discerned from the upper side. The female is much larger than typical specimens of 4. eupheno, agreeing with the male in markings and in the shape and greater depth of the fore wings. The orange blotch, instead of being con- fined to the tip of the fore wing in the usual manner, extends as far asthe discoidal spot and is bounded (usually) on its inner margin by a black band, which sometimes suffuses the whole tip of the wing. The ground colour of the fore wing varies from pure white to pale 1886.) CAPT. R. G. W. RAMSAY ON A NEW COPSYCHUS. 123 lemon ; the hind wings are always yellower than in the typical form, in some specimens being nearly as dark as in the males. The markings of the underside of the hind wings are very indistinct, they are usually of a greyish-green tint, but sometimes approach a rusty-red colour which is found in the typical form, although both forms occur in Algeria. This distinct local form I took at Mogador in March 1885. It was somewhat common at a little distance from the town; the females, as is always the case in this genus, being much scarcer than the males. I have only been deterred from describing this variety as a new species by the kindness of M. C. Oberthiir in forwarding me a specimen of 4. eupheno from Central Algeria, which is intermediate between the above-described variety and the type. Similar cases of the two sexes (usually very different) approaching the same form of colouring are not uncommon ; for example—Lycena alexis, in many localities; Hepialis humuli, in Shetland ; Odones- tris potatoria, in which it is not unusual to find males with the paler colouring of the females, and females possessed of the darker tint of the males. 6. On a new Species of Bird of the genus Copsychus. By R. G. Warptaw Ramsay, F.Z.S., F.L.S. [Received February 2, 1886.] Among a few birds which I obtained some months ago out of a collection made by Mr. Harry Pryer at Elopura, in N.E. Borneo, are examples of a very interesting and hitherto undescribed species of the genus Copsychus. Mr. R. B. Sharpe, in his ‘Catalogue of the Birds in the British Museum,’ has recognized three good species of Copsychus, viz, :— 1, C. mindanensis. 2. (. seychellarum. 3. C. saularis. Under the latter he treats as local races C. musicus and C. ameenus. Iam inclined to doubt the propriety of uniting C. amenus to C. saularis, and prefer to keep it distinct. The new species, which I propose to name Copsychus niger, is of about the same size as C. amenus, from which it differs in having a much smaller amount of white on the wing-coverts and none on the secondaries and in having the tail entirely black. In its general appearance it more resembles C. seychellarum, which, however, has its black plumage glossed with green instead of blue as in C, niger and the other species of the genus. Length 9-2, wing 4°35, tarsus 1°25, tail 4°5, bill from gape 1°25 inches. 124 THE SECRETARY ON ADDITIONS TO THE MENAGERIE. [Feb. 16, The five species may be easily distinguished as follows :— 1. C. seychellarum. \ ) (Seychelles.) | } Belly black. 2. C. niger. | (N.E. Borneo.) ) ¢ Tail entirely black. 3. C. mindanensis. Belly white. (Philippine Islands.) ) / 4, C. amenus. Belly black. (Jaya, Borneo.) | 5. C. saularis. Belly white. : : (Ceylon, India, Assam, ee tail-feathers white. I ) to Malay Peninsula, and China, Andaman Islands, Sumatra, Java, Borneo.) February 16, 1886. Prof. W. H. Flower, LL.D., F.R.S., President, in the Chair. The Secretary read the following report on the additions to the Society’s Menagerie during the month of January 1886 :— The total number of registered additions to the Society’s Mena- gerie during the month of January was 97. Of these 9 were by birth, 64 by presentation, 12 by purchase, 8 by exchange, and 4 were received on deposit. The total number of departures during the same period, by death and removals, was 118. ‘The most noticeable additions during the month were :— 1. A Many-marked Snake (hagerrhis multimaculata), presented by the Rev. G. H.R. Fisk, C.M.Z.S., and received January 1, 1886. Amongst several collections of the Snakes of the Cape Colony lately received from our excellent correspondent is a single small example, about a foot long, of this species, as kindly determined for us by Dr. Giinther. It is the Coronella multimaculata of Smith (Illust. Zool. of South Africa, pl. 61), but properly referable to the genus Rhagerrhis of Peters (Monatsb. k. Preuss. Ak. Wissen. Berlin, 1862, . 274). ‘ 2: ight Tree-Snakes, born alive in the Society’s Reptile House, on the 9th of January. The mother, a fine example of Dryophis prasina, presented by Dr. F. H. Bauer, C.M.Z.S., of Buitenzorg, Java, was received on the 15th of August last, so that she must have been for upwards of five months without any possibility of intercourse with a male of the same species. The young ones were all born on the same day at irregular intervals between 11 a.m. and 4.30 p.m. They were removed to another case, where they quickly Ca rt pie Ri tet Pee ee NN pias Fine Meth ia ‘Qpn'g -wbhoy "TINVNNAd VISLISAW 4oSTInNNS Ar AN Verona Pr “UL PP testy BuO Y 2 ‘dum sougq wue pry] 1886. | MR. O. THOMAS ON CRANIAL VARIATION. 125 took refuge amongst the leaves of a fresh plant. Although they have not fed, they seem to be lively and doing well’. Mr. Sclater exhibited a specimen of the new Paradise Bird, Paradisornis rudolphi, lately discovered in the Owen Stanley Mountains of New Guinea by Mr. Hunstein, and described and figured by Drs. Finsch and Meyer in a recent number of the ‘Zeitschrift fiir die Gesammte Ornithologie’ (1885, p. 385), and pointed out the characters in which it differs from typical Paradisea. The Secretary exhibited on behalf of Mr. L. Taczanowski, C.M.Z.S., the skin of an Owl from the south-east of the Ussuri country, on the frontiers of Corea, which appeared to be referable to Budo blakistoni, Seebohm, P.Z.S. 1883, p. 466, and Ibis, 1884, p. 42 et p. 183, 1. vi. : Two adult females of this Owl had been obtained by Mr. J. Kalinowsky, during his recent stay in Kamtschatka, from the environs of the river Sidemi in Russian Mantchuria, on the frontiers of Corea, where they were collected in the latter part of May 1885. They appeared to agree with Japanese specimens of B. blakistoni in the National Collection, where Mr. Sharpe had kindly made the comparisons. Mr. Edward Gerrard, Juu., exhibited specimens of the heads and skulls of two African Rhinoceroses (Rhinoceros bicornis and R. simus), obtained by Mr. Selons in Mashuna-land, and mounted for the South-African Museum, Capetown. Prof. Ray Lankester exhibited and made remarks on a drawing of a restoration of Archeopteryx. The following papers were read :— 1. Notes on a striking instance of Cranial Variation due to Age. By Oxprietp Tuomas, Natural History Museum, [Received February 16, 1886. ] (Plate XI.) Dr. Gulliver, of St. Thomas’s Hospital, has recently submitted to me for determination three skulls from Canada, collected by Mr. Hayden. The skulls turn out to be referable to the fairly common Canadian Marten or Pekan (Mustela pennanti, Erxl.), but they show to such a remarkable extent the cranial changes that occur in * See Miss Hopley’s account of this event in ‘Nature,’ vol. xxxiii, p. 295. 126 MR. 0. THOMAS ON CRANIAL VARIATION. __[Feb. 16, later life among this group of animals, that I have thought it worth while to have them figured, and to make a few notes on the causes and extent of the changes presented by them. This is the more called for owing to Mammalogists who have not access to large series of specimens being as a rule far too ignorant of these changes to judge by the numerous so-called “new species’? which are constantly being described on variations of a corresponding nature. These changes have been pointed out at various times, as for example by Berthold’, Nathusius*, Hensel *, and others; and the object of the present paper is therefore merely to give further publicity to a fact which has a very considerable bearing on the value of the cranial differences brought forward as characteristics of freshly-described species. The three skulls, which I will speak of as A, B, and C, consist evidently of two males and one female, the latter being far smaller and lighter than the other two. Of their specific identity there can be absolutely no question, although I have found it difficult to make most people to whom I have shown them believe in that fact. B (Plate XT. fig. B) is a skull of the ordinary type, showing no special peculiarities ; it is fully adult, as is proved by the basilar, sphenoid, and other cranial sutures being closed, although some of the facial ones are still visible, and by the teeth showing signs of commencing wear. Compared to such a skull as this, the aged skull A (fig. A) shows the changes that take place in later life to a most remarkable extent, well worthy of some special notice. All the changes are connected with an increase in the power of biting, and the consequent development of the biting muscles, but the connection of some of the changes with the biting muscles is not so obvious at first sight as to be readily perceived by any one not specially on the look-out for it. To commence with, the canines of A are apparently very much longer and more powerful than those of B, a difference not due to individual variation, but to the fact that they are as a whole pushed further outwards as time goes on and additional dentiné is deposited round their bases ; the absolute length of the enamel-covered portion from the cingulum to the tip being precisely the same in both. The next difference is one too commonly recognized to need much remark, viz. the development of the occipital crest; but it is here carried to a relative extent greater than in any other skull I know of, not even excepting the Hyzenas and Sea-lions. In B the crest has scarcely commenced to grow at all, while in A it is no less than 20 millim. (nearly an inch) in vertical height above the brain-case. The temporal muscles, passing from these enormous crests down through the zygomata to the lower jaw, have then by their constant pressure on the bone caused it to absorb in certain places, and have thus induced three remarkable changes in the skull that might easily be, and have in fact often been, taken as marks of specific distinction. Firstly, they have pressed against and bowed outwards the zygomata, 1 Tsis, 1830, p. 570. 2 Arch, f. Nat. iv. p. 130 (1838). 3 “ Craniologische Studien,” N. Act. Ac. Nat. Cur. xlii. p. 127 (1881). 1886. ] MR. O. THOMAS ON CRANIAL VARIATION. 127 until the zygomatic spread in A is no less than 74 per cent. of the length of the skull, as compared to 59 per cent. in B, the actual breadth being nearly one third greater. Secondly, they have pressed upon the inner walls of the temporal fossee, and have thereby reduced the breadth of the skull at the interorbital constriction to such a degree that in A its least width is only 16 millim. (36 per cent. of the basi- cranial axis) as compared to 23°5 millim. (57 per cent.) in B. That the width at this constriction grows absolutely, as well as relatively, less in many mammals has been observed by several authors, but it is, I think, by no means sufficiently realized. Thirdly, the great biting ‘muscles have pressed upon and thereby constricted the posterior narial passage, its outside breadth being only 10°5 millim. in A as against 11°9 in Bt Inside the brain-case again, the con- striction of its anterior part has reduced the cranial capacity from 40 c.cm., as it is in B, to 35 in A, the smaller capacity being therefore found in the larger and older skull. These various differences are shown in the drawing (Pl. XI.) better than they can be explained by any amount of description. Finally, I would again lay special stress on the fact that B is absolutely adult, so far as any definition of adult age can be drawn up, and has therefore no sign whatever of immaturity, such as would put the species-maker on his guard, and yet that in a skull so adult as this such changes may take place in advanced life as to alter its whole appearance and proportions, and even its cranial capacity. To disprove the natural suggestion that the differences above noted are due to sex, there comes fortunately the skull C, collected at the same time and place, which in its age-characters is intermediate between A and B, but is far smaller and more lightly built, and is quite obviously the female form corresponding to the other two. The following are the measurements of the three skulls for comparison :— A. d. 1 Ay alll aye Peneth*... .. ... STS. RE SEAMPT H ip 107 93 Greatest breadth . ........ AP RB: 63 56 Beate, Tent oa. ws ae. 63 60 52 mee teadth 2.4. tes ace OO 34 ok Interorbital constriction... ...... 16 23°5 19 RASICIAMIAL AXIS? «.... 0. os «0..< 45 4] 35 Capacity (in cubic centimetres)... 35 40 31 * Basion to front of premaxillx. * Basion to anterior edge of basisphenoid. 128 MR. W. L. SCLATER ON A NEW [Feb. 16, 2. On a new Madreporarian Coral of the Genus Stephanotro- chus from the British Seas, with Notes on its Anatomy. By W. L. Scuater, B.A., F.Z.S., Assistant to the Jodrell Professor of Zoology, University College, London. [Received February 15, 1886.] (Plates XII.—XIV.) I. Introductory remarks, p. 128. | IV. Distribution of the genus Ste- II. Description of the Corallum, phanotrochus, p. 182. p- 128. V. Anatomy of S. moseleyanus, TII, Comparison of S. moseleyanus . 182. with other species of the VI. List of publications on the sub- genus, p. 180. ject, p. 135. I. Introductory. Professor Moseley has kindly placed in my hands for examination and description a specimen of a Madreporarian coral, which I have now the pleasure of exhibiting to the Society. The coral is of much interest, as being the finest and largest of the genus Stephanotrochus, lately instituted by Professor Moseley (1)* (‘ Challenger’ Report on Corals, p. 151), and also as being the first example of this form that has been dredged in British seas. The coral is a solitary form; it was procured on the expedition of H.M.S. ‘Triton’ in the summer of 1882: “station 13; August 31st, 1882, lat. 59° 51’ 2" N., long. 8° 18’ W.; depth 570 fathoms ; bottom, ooze ; bottom temperature, 45°7 F.(7°°7C.). Trawl.” Station 13 is situated almost in a straight line and about halfway between the Farée Isles and the northeru point of the Hebrides ; it lies to the south-west of the Wyville-Thomson ridge, so that it is well within the warm area described by Murray and Tizard (2). The coral is interesting, since it is by far the largest solitary form that has yet been discovered in British seas ; its nearest allies were dredged off the Azores and Pernambuco during the ‘Challenger ’ Expedition. The coral was well preserved in absolute alcohol, so that Ihave been able to make a fairly satisfactory investigation of its anatomy by means of sections and other microscopical preparations. It is to the kindness of Professor Moseley that I am indebted for this coral ; and since the genus and the other four species belonging to it were all described by him in his report on the ‘ Challenger’ Corals, I propose to dedicate this new British species to him under the name of SrEPHANOTROCHUS MOSELEYANUS. II. Description of the Corallum. The corallum is white where covered by the soft tissues; the base is of a bluish-grey colour ; it is saucer-shaped, the base being very nearly flat, but forming a very low cone; and from this base the side-walls of the theca rise, making an angle of about 60°. In the centre of the base is a very small pedicel of attachment ; 1 The numbers refer to the List of Publications at the end of the paper. 1886. | MADREPORARIAN CORAL. 129 there was no trace of any shell or other foreign body to be detected as was the case with two other species of the same genus as described by Prof. Moseley (1, page 154). From the pedicel radiate cost corre- sponding to the primary, secondary, and tertiary septa. The cost are formed by ridges along which are a series of blunt points. Between the basal costze the corallum is granulated, the granules running in lines and corresponding, not to the septa, but to the interstices between them. On the side-wall of the corallum, however, the ridges and points become much sharper, and there arise costee corresponding to the quaternary and quinary septa; these are smooth and do not bear the points with which the primary, secondary, and tertiary coste are provided. The single specimen from which this species is described has unfortunately been broken and has re-mended itself, so that it is malformed, for there are only nine larger septa (7. e. primary and secondary) ; no doubt had the specimen been an uninjured one it would have possessed the typical Madreporarian number of twelve (i. e. six primary and six secondary ). The coral will therefore be described on this assumption. There are five cycles of septa—six primary, six secondary, twelve tertiary, and forty-eight quinary, in all ninety-six. The secondary septa are distinguished from the primary by bearing large stout pallial elevations, each septum bearing two, the smaller one being the more central; the primary septa also bear pali, but they are not so large or distinct as those of the secondary septa. The tertiary septa are also slightly thickened at their inner ends. The ends of the primary, secondary, and tertiary septa are all fused with avery thick up-rising of calcareous matter, the columella, which bears five or six rounded projections resembling the true pali, but much lower, showing how the columella has been formed by the central ends of the septa and their pali. This knobby top of the columella forms a floor to the central part of the enteron of the polype, and it is much shallower than the surrounding chambers between the septa, where the floor is formed by the true base of the corallum. The quaternary septa do not quite reach the columella, but they are bent inwards so as to touch the tertiaries ; those lying to the immediate left of the tertiary septum being shorter and joining the tertiary septum at a point nearer the circumference than those on the right, as is best seen in the figure (Plate XII. fig. 1). The quinary septa are much shorter than the others, only reaching halfway along the base of the theca and ending in two small upgrowths which seem to represent two rudimentary pali; no rudiments of pali could be seen on the quaternaries. All the septa are extremely exsert, the primary and secondary septa more especially so, so that in the specimen the tissues did not cover their sharp edges; but this is probably due to the contraction caused by the spirit. It is only the outer halves of the primary and secondary septa Proc. Zoot. Soc.—1886, No. IX. 130 MR. W. L. SCLATER ON A NEW (Feb. 16, that are so prominent, the edge towards the columella dips down so that the septum has a strongly concave upper margin, as is shown in the figure (Plate XIII. fig. 5). The quinaries resemble the primaries and secondaries in shape, but are of course much smaller; those quinaries which are adjacent to the primaries and secondaries being much larger and more promi- nent than those adjacent to the tertiaries, and joined to the primaries and secondaries by an upgrowth of the wall. The tertiaries and quaternaries resemble one another, since they both have a straight upper margin, not concave as is that of the primaries, secondaries, and quinaries. All these details with regard to the arrangement of the septa will be best understood by the examination of the drawing (Plate XII. fig. 1), which gives a diagrammatic representation of the septa, tentacles, and mesenteries. All the septa are covered with granules arranged in lines showing the lines of growth. The measurements are as follows :—longer diameter 5 centims. ; shorter diameter 44 centims. ; height of the corallum from the base to the tip of the highest septum 2 centims.; height of the edge of the cup | centim. III. Comparison of Stephanotrochus moseleyanus with other Species of the Genus. In comparing S. moseleyanus with other species of the genus Stephanotrochus, which are four in number, all described by Mose- ley, from the deep sea, the first point that is noticed is the much greater development of the pali, which in all the other species are merely slight thickenings of the internal ends of the septa, but which in S. moseleyanus form a crown of stout upgrowths, supporting the internal edge of the oval disk. Again, compared with all the other species of the genus, the primary and secondary septa are very much stouter and more exsert, the line between the palus and the other end of the septum is very much more concave (see Plate XII. fig. 5). The septa form five complete cycles, and are remarkable for their regularity ; this is also the case in §. diadema, but not in the other species of the genus. There is no plain distinction of size between the primary and second- ary septa in S. moseleyanus as there is in S. platypus, diadema, and discoides ; but the primary and secondary septa are equal in size, and can only be distinguished by their position with regard to the long axis of the coral, as in S. nobilis. On the other hand, S. moseleyanus agrees best in general shape with S. diadema and platypus, and differs from S. nobilis, in which the corallum is deep and cup-shaped, whereas that of S. mosleyanus is flat and saucer-shaped. The differences between the five species are shown by the accom- panying diagrams (p. 131), which illustrate the arrangement of the septa in each species of the genus ; it will be seen that S. moseleyanus agrees best with S. platypus in this matter, from which it differs only in having the internal ends of the quaternaries turned in on to the tertiaries, “while in S. platypus all the septa are quite straight. 1886. ] MADREPORARIAN CORAL. 131 Fig. 4 Fig. 5. Diagrams of the arrangement of the septa in the five different species of Stephanotrochus. The septa are numbered. 1. S. nobilis. 2. S. platypus. 3. S.diadema. 4, S. discoides. 5. S.moseleyanu 132 MR. W. L. SCLATER ON A NEW [ Feb. 16, The genus Stephanotrochus belongs to the section of the Madre- poraria known as the Madreporaria aporosa, to the family Turbi- nolidze of Milne-Edwards and Haime, and to thesection Discocyathoida of Martin Duncan (3), which is characterized as follows :—“ Simple - Turbinolidze, discoid in shape, not increasing much in height with growth. Free or not. With or without pali in one crown. Colu- mella variable; epitheca also.” Stephanotrochus moseleyanus agrees in every way with the above definition except in the point about the pali, since in S. moseleyanus there are distinctly two crowns of pali. IV. Distribution of the Genus Stephanotrochus. All the species of Stephanotrochus hitherto described are deep-sea forms, the depths from which they come varying from 410 to 1009 fathoms ; S. moseleyanus comes from a depth of 570 fathoms. The geographical distribution, considering the fewness of the specimens dredged, is extraordinary ; seven specimens have been obtained belonging to five different species, procured from such distantly separated places as Pernambuco, the Azores, Sydney, N.S.W., and the Faroe Channel. As was mentioned above, S. moseleyanus was dredged in the warm - area of the Faroe Channel, where the bottom temperature is very high, 46°5 F. V. Anatomy of Stephanotrochus moseleyanus. The soft tissues of the polype extend from the edge of the cup some distance down the outside wall of the corallum, gradually thinning out; the line of the extension of the soft parts is marked in the dry corallum by the change of colour from a glistening white to a greyish blue, the colour of the basal parts uncovered by soft tissues. As far as I was able to observe, the enteric cavity does extend round the edge of the theca to the outer side, so that the tops of the smaller septa would probably stand up free in the enteron; the primary and secondary septa are so extremely exsert that the tissues are abnormally stretched to cover them, and so have by the action of the alcohol been split. This would rather seem to confirm Koch’s theory (5) that the theca is formed from the fused peripheral ends of the septa. The oral disk, the tentacles, except at their tips, and the outer soft wall of the coral are all of a dark madder-colour ; this colour is due to a substance called by Prof. Moseley (6) Polyperythrin ; it is distin- guished by peculiar properties: it is insoluble in water, glycerine, al- cohol, ether, ammonia, potash, or picric acid, but is soluble in strong hydrochloric acid ; it is also distinguished by a peculiar absorption spectrum, a broad black line including the line D. Prof. Moseley found it in Stephanotrochus diadema, in Flabellum, Fungia, and Ste- planophyllia, and many other Ccelenterata. The soft wall of the coral is divided up by a series of longi- tudinal furrows, which correspond to the insertions of the mesenteries ; the ridges between the furrows are further crossed by a number of transverse ridges, so that the whole wall assumes a very wrinkled 1886. | MADREPORARIAN CORAL. 133 appearance, doubtless exaggerated by the action of the alcohol in which the coral is preserved. The tentacles are in four cycles ; the innermost cycle are of the largest size, and correspond in position to the primary aud secondary septa, and are therefore tweive in number. The second cycle correspond to the tertiary septa, and are also twelve in number. The third cycle correspond to the quaternaries, and are twenty-four innumber. These differences between the three cycles are very slight, consisting only of small differences in size. The fourth cycle, placed considerably nearer the circumference of the coral, are very much shorter and more stumpy than the other three cycles; they correspond to the quinary septa, and, as will be seen below, are evaginations of intermesenterial spaces [exoccelic, Fowler, (4)], not of the inéra- mesenterial chambers [entoccelic, Fowler (4) | as are the others ; they are forty-eight in number ; so that there are altogether ninety-six tentacles. ' The mesenterial chambers are forty-eight in number; there are two cycles of mesenteries, larger and smaller, forming larger and smaller chambers ; the larger chambers contain septa of the first, second, and third order; the smaller chambers septa of the fourth order. From these chambers the tentacles of the first three cycles are evaginated ; the fifth cycle of septa, on the other hand, are placed in the spaces between the mesenterial chambers, 7. e. exosepta, Fowler ; and the fourth cycle of tentacles are in the same way evaginated from these exoccelic spaces. The whole arrangement will best be under- stood by reference to the diagram (Plate XII.). In all the chambers, with the exception of those in which are placed the primary septa situated at the long ends of oval mouth- opening, the longitudinal muscles are placed, facing one another ; but in the chambers above mentioned, the muscles are placed on the outer faces of the mesenteries; these therefore are the directive mesenteries. So that in the arrangement of the muscles on the mesenteries, Stephanotrochus exactly corresponds to the Hexactinian type, as do all other Madreporarian corals that have been hitherto examined. The tentacles are all of one shape, they are simple conical evagina- tions of the ccelenteron ; they end in a knob separated from the rest of the tentacle by a narrow neck; the knob contains no pigment, and is of a white colour; the main part of the tentacle is madder-coloured like the rest of the polype. A section of the knob and part of the conical part of the tentacle is figured (Plate XIII. fig. 6); the knob is packed full of nematocysts, and in fact isa single immense battery of thread-cells. The ectoderm consists of a series of very long and very narrow cells, which are nucleated ; there are also gland-cells present, but the elements are difficult to distinguish ; the endoderm cells of the knob are much longer than those lining the other parts of the ccelomic cavity of the tentacle. I was unable to distinguish any muscular elements in the knob; it is perhaps in consequence of this that the outline of the knob appears straight, since it apparently has not been contracted by the action of the spirit, as has been the rest of the tentacle. 134 MR. W. L. SCLATER ON A NEW [Feb. 16, The ectoderm of the tentacle (Plate XIII. fig. 6) also contains a series of nematocyst batteries; the cells, however, differ from those of the knob in the following points: they are very much smaller, they are pigmented, from them are developed the longitudinal muscle- fibres ; in the endoderm of the main part of the tentacle the elements are not nearly so high as are those of the knob, and at their bases are found the circular muscle-fibres. The tentacle therefore differs little in structure from the actinian type as deseribed by Hertwig (7). The muscles are very weli developed on both sides of the mesen- teries ; the arrangement is shown in figures 8 and 9 of Plate XIV., where figure 8 represents the arrangement on the ectoccelic face, figure 9 the arrangement on the entoccelic face. The edge of the mesentery is occupied by a thick packed mass of mesenteric filaments above, and by the ova, also packed thick, below ; ova and mesenteric filaments seem to be well developed in all the mesenteries, except on the directives, where I have been unable to detect any sign of ova, but I have only been able to examine two directives, one of which was malformed, so that I am unable to make sure of this point. Plate XIII. fig. 7 represents a small portion of a section of a mesentery highly magnified, showing the folding of the surface on one side in order to increase the surface for the muscle-slips, but in no case have I detected the inclusion of masses of muscles in the mesoderm, as has been figured by Hertwig (7) m Aetinolobia and Tealia, and other Actiniz. The only example of this Coral I have been able to examine con- tained ova; no spermatozoa could be detected, so that the Coral may be considered dicecious. The development of the ova differs slightly from that described in the Actinians by Hertwig ; in Stephanotrochus the mesodermal lamella in which the ova lie is reduced to a thin string (Plate XIV. fig. 10), and the entodermal cells on either side have become very long and thin, resembling, perhaps, the ‘‘ Cambium Zellen” described by Weissman in certain Hydroids which nourish the ova at their own expense. In. the figure there will be seen several ovarian cells which have not yet entered the mesodermal lamella, but which are still lying in the endoderm ; and in one case there is an ovarian cell figured lying half in the endoderm and half in the mesodermal lamella; the ripe ovum is full of deutoplasm, and the germinal vesicle and germinal spot are very clearly seen. Besides the ovarian string, the mesenteric filaments can be seen in section ( Plate XIV. fig. 10), consisting of a mesodermal string and high endodermal cells, with many pigment-cells scattered among them ; they are cut in section in different planes. Beyond the ova the mesoderm again thickens slightly up to the end of the mesentery, where it splits to line the hard septal walls, since this section is from part of the mesentery low down where the mesentery is inserted between the columella and the two adjacent septa, all of which are lined by the mesodermal lamella with a layer of calycoblastic cells interposed. Calycoblastic cells were first detected by Heider (8), who showed 1886. ] MADREPURARIAN CORAL. 135 that all the hard parts of the coral are laid down by these cells, which can be always found between the mesodermal lamella and the hard parts. Koch (9) showed that the calycoblasts were really the remains of the basal ectoderm-cells of the embryo, so that the whole of the corallum is laid down by ectoderm, and is really, mor- phologically, outside the coral. This of course corrects the old view which regarded the basal ectoderm of a coral as having disappeared from the outside of the corallum, since what remains of the basal ectoderm is really within the corallum, and is the very means of forming the corallum. Koch (9, plate xx. fig. 9) gives a repre- sentation of three calycoblastic cells, which seem to be merely ordinary high epithelial cells, nucleated and filled with granules. I have found everywhere between the corallum and the mesoderm lamella a tissue or series of cells, represented in Plate XIV. figs. 10-13, cal. ; these I believe to be the calycoblasts described by Heider and Koch. That these cells must be calycoblasts is, I think, evident from their position, since they are everywhere found between the corallum and the mesoderm lamella. But in form they are very different from the calycoblasts figured by Koch, for, whereas Koch’s calycoblasts are, as was said above, ordinary granulated epidermic cells, the cells which I have found in Stephanotrochus are not quadrangular but of irregular shape, and separated from one another by intervals, so that they seldom form a definite layer; also they are striated in a most extraordinary way, as is shown in figure 12. Whether these cells are the calycoblasts of Koch I cannot with certainty say; it may be that the difference of appearance is due to the fact that Koch’s figure represents these cells in a very young state, when they are doubtless more active than in the adult coral; or, again, the calycoblasts of Koch’s form OPC bas | Puate XIV. Fig. 8. Ectoccelic face of a larger mesentery, showing arrangement of muscle- fibre lines: m/f. mesenterial filaments; 0, ova. 9, Entoccelie face of the same mesentery, showing the longitudinal muscle- fibre lines. 10, Longitudinal section of the ventral end of a mesentery: cal, calyco- blasts which lay down the columella; M, mesoderm; ov, ova in all stages of development; Ln, endoderm; .f, mesenterial filaments with pigment-cells, p. 11. Central end of a mesentery, with calycoblasts scattered all along the corallum-facing side of the mesoderm; the mesodermal Jamella of the mesentery splits to line the columella on each side, and then twmns back to line the septum. 12. Shows two isolated calycoblastie cells. 13. Drawn from a flat preparation of ealycoblastie cells. a ‘| : roe is WL del P Smit th. Mintern Bros. xmp STEPHANOTROCHUS MOSELEYANUS \ \\ ! \ i \ N \ USE (| Mintern Bros.imp. STEPHANOTROCHUS MOSELEYANUS ce a. . :x | = = ~* ¢« e € — 1 = » “> q . i a « 5 / . 7— 3 > = = . ‘ al a A 7 > oe - ‘et a = a - 9 a a . —.' “fe «-* - * S — - ™— ” =r ‘ + a > <— . ae . - ' — 7 - ’ 4 ra = j ’ ~ ad ~ ’ —" : . . ‘ . 3 : - ~ Km i = = “ 2 : ‘ e * a » a4 “ ~ - * ~~ 4 = Pooky = <, « - a2 tS . * 3 * « : s ~~ * - . F - » ae rf ., y Pind ~, o « | 4 Py ee ‘ - = * x - “4 ‘ ‘ PF * ¢ = na 4 a ’ . . * La >» ; . “A eT a a oo * d ~ < Se, ie oS ; a > fA ad « * 7 » 3 .* * a ‘ » oN - i a ewe > ’ 2 « Py 2 P.Z.S. 1866. P1. xiv. cal ; @ e@gaee” Ya in a a tthe QZ => IIS MANEATIS 24 pal iy Oh Ym. Mintern Bros. imp. STEPHANOTROCHUS MOSELEYANUS. 1886.] MR. COCKERELL ON PARMACELLA VALENCIENNESI. 137 March 2, 1886. Dr. St. George Mivart, F.R.S., Vice-President, in the Chair. The Secretary read the following report on the additions made to the Society’s Menagerie during the month of February 1886 :— The total number of registered additions to the Society’s Mena- gerie during the month of February was 79, of which 3 were by birth, 40 by presentation, 14 by purchase, 1 by exchange, and 21 * were received on deposit. The total number of departures during the same period, by death and removals, was 99. Amongst the additions during the month attention may be called to :— 1. Five examples of a large Batrachian of the Argentine Republic, there called ‘‘ Escuerzo”’ (Ceratophrys ornata), presented by Dr. Frederick C. Strutt, and received February 13th. 2. A Mantled Buzzard (Leucopternis palliata) from Brazil, pur- chased February 15th, being the first example of this fine bird of prey received by the Society. Mr. John G. Millais, F.Z.S., exhibited an adult male specimen of the Ivory Gull (Larus eburneus), which he had shot himself at Thurso, Caithness, on December 30, 1885, during a severe snowstorm from the north. The base of the bill to the end of the nostril in living specimen was light blue, and the point of the same orange-yellow ; feet black, and eye surrounded by a ring of orange; the rest of the plumage being entirely white. Mr. Millais also exhibited an immature specimen of the same species killed at East Haven, Forfar, in January 1879. Mr. T. D. Cockerell exhibited a living specimen of a variety of Parmacella valenciennesi, Webb and Van Beneden, collected by J. H. Ponsonby, Ksq., at Tangier, and made the following remarks :—The specimen differs from the typical P. valenciennesi in that it is marked with black, the original figure of the species being quite uniform. It may possibly prove to be distinct, but until further details are ascertained it is best classed merely as a variety of P. valenciennest. A precisely similar form is found at Gibraltar, of which there are details in {he ‘Journal of Couchology ’ for January 1886. The following papers were read :— Proc, Zoox, Soc.—1886, No. x. 10 Zau\SH, Migs CLAN ae D) 138 PROF. R. COLLETT ON A . [Mar. 2, 1. On a new Pediculate Fish from the Sea off Madeira. By Rosert Cotzerr, C.M.ZS. [Received February 12, 1886.] (Plate XV.) Fam. CERATIID. LINOPHRYNE, 0. gen. Head enormous ; the body slender, compressed, mouth oblique. Spinous dorsal reduced to a single cephalic tentacle, the basal part of which is erect, not procumbent. Teeth in the jaws, on the vomer, and the upper pharyngeals. Gill-openings exceedingly narrow, situated a little below the root of the pectorals. Soft dorsal and anal very short; ventrals none. Abdominal cavity forming a sac, suspended from ‘the trunk. Skin smooth; a long tentacle on the throat. LINOPHRYNE LUCIFER, Sp. noy. (Plate XV.) The head tetrahedral, with a supraorbital spine ; its length is to the total length as 1 to 2:7. Eyes small, situated high up on the side of the head. Teeth of the jaws uniserial, very long; 7 to 9 on each side in each jaw; one or two in front longer than the others ; all are movable inwards and covered with skin. Gill-openings narrower than the diameter of the eye. Length of the intermaxillary bone is contained three times in the total length. Cephalic tentacle thick, with a large bulb; the guttural tentacle long, with the end cleft and provided with small papille. Colour uniformly black, the top of the cephalic tentacle and the papille of the guttural tentacle white (phosphorescent ?). Total length of the single specimen 49 millim. iD: lL; 2-D.3;-A. 2; P.14-15; C. 9: Habitat. One ‘specimen, total length 49 millim., from the sea off Madeira (36° N. lat., 20° W. long.), May 1877; preserved in the Zoological Museum at Christiania. Measurements. millim Total length to the end of the caudal fin .............. 49 Length to the root of the caudal fin ...... 35 Length of the head to the hind margin of the operculum. . 18 35 to the end of its spine ba hE ra 22 Length from the snout to the hinder margin of the eye. . 9 Length to the edge of the distended abdominal sac ...... 39 Length of intermaxillary ee CR A wih. ka os eis. eae 16 Length offlawerqawig — opis cs ee sou ins vas vo ae ee Breadth of thetswergaw..)i05 02... juntas <5 22 eka 4°5 The greatest depth of the head ...-.. 0.00.5 c0-- 6s-s 0s 19 The depth of the head from the base of the orbital spine . 10 1886.] NEW PEDICULATE FISH. 139 millim Breadth of the head across the jaws .................. 16 a fe across the base of the orbital spine .. 10 Length of the body to the commencement of the second UTC Seer Nr es ee Oneal one einen aes 26 abe dine of. the second dorsal + ...).0) <<. )sie's a, see die, vive « O Depth of the root of the tail), 2.0% 0< 4 osu0s nis bee he Oe PUREED OES ORE fio fac ciehic, ‘as finds ands re detente sda ve 2°5 Length of the cephalic tentacle (first dorsal)........ ... 9 Length of the guttural tentacle ...............-.. 0005 23 Renetn othe! Sandal fie.) 251. poghi winters alhiares al4O Length of the pectorals (with the pseudobrachium) .. .... 5 Length from the snout to the pectorals (to the root of pseudo- DCRG eh dete etey Fs tndrstais 4 b.<45. oxiumssubi tev heaanen dG The structure of the body in its natural state can hardly be correctly described from this specimen, in which the whole of the belly exhibits an abnormal distension in consequence of the fish having swallowed a Scopeloid fish, the total length of which is one half longer than itself. The head is very large, with an enormous mouth and long teeth. The body itself is short and slender, compressed, and with the heavy dependent abdominal cavity, of which the hindermost part extends far beyond the end of the vertebral column. The greatest depth of the body is at the back of the head, and is precisely the same as the length of the head. The body itself is apparently much lower, and the root of the tail narrow and low. A thick cephalic spine is to be found on the snout; and under the throat a long tentacle divided at the end, which undoubtedly is phosphorescent, as well as the end of the cephalic spine. The gill-openings are so narrow that they can only be distinguished with difficulty ; their openings are not much larger than the head of a pin. Lhe head.—Its appearance when viewed from the front is nearly tetrahedral, somewhat compressed, and broadest downwards. Its greatest width is across the angle of the mouth, and is about equal to the length of the intermaxillary bones. The upper profile of the head exhibits a somewhat projecting and slightly outwardly inclined spine above each eye. The breadth of the head across the base of these spines (which form the upper corners of the square when the head is seen from the front) is one third less than the breadth across the angles of the mouth (or the lower corners of the square). The forehead in front of the orbital spines is concave, with a deep furrow leading to the end of the snout, bounded on each side by a ridge, on which also the orbital spines are projecting ; the concavity is somewhat broader downwards than it is above. There are altogether three spines on each side of the head. One orbital spine is directed upwards and slightly forwards. One spine at the back of the operculum is directed backwards ; also a small spine at the back of the lower jaw sloping inwards and downwards ; 10* 140 PROF. R. COLLETT ON A [Mar. 2, the last is, however, in the uninjured specimen scarcely perceptible beyond the common skin which covers the head. The length of the head from the end of the lower jaw to the base of the spine on the operculum is to the total length as 1 to 2°7, this measured to the end of the caudal fin, but only 1:9 in the length to the root of the caudal. Thus the head is about the same as the rest of the body without the caudal fin. The highest part of the skull is indicated by a protuberance at the back of the head, probably formed by the point in which the os mastoideum (occipit. posterius) adjoins to the shoulder-girdle. The mouth is enormously large, with the cleft oblique; the lower jaw is slightly longer than the intermaxillary, and has backwards a considerable width (or about 7 of its length). The length of the jaws is to the total length (to the end of caudal fin) as 1 to 2°8-3°0. At the back of the lower jaw there is a spine slanting inwards and downwards, the length of which scarcely equals the orbital spines. The eyes are well developed, although small on the whole; the lens is particularly small (about 1 millim.). The diameter of the eye is about 2°5 millim. ; it is placed somewhat far forward, or a little more than two orbital diameters from the margin of the upper jaw. The gill-covers are but incompletely ossified, but their construction cannot be properly examined in this single specimen. The operculum is present as a long styliform bone, which towards its lowest end sends out a backward-directed spine the length of which is 3 millim. (which, however, is completely enveloped in the common skin of the head). tthe preoperculum appears to be unossified. The gill-openings are extremely small, and are situated at a distance of about half an eye’s diameter below the pectoral fins; they form a crescent-formed slit, the height of which is only 2:2 millim. The gills are 24 pairs, as the second and third branchial arches have a double series, the fourth a uniserial gill. Pseudobranchie are wanting. The branchial arches are smooth on their inner surface, without a trace of protuberance or teeth. The branchiostegals appear to be but five in number; and I cannot, in this little and frail specimen, discover a sixth, which may possibly exist. The feeth are placed in a single row in each half jaw, with a distinct space between each tooth, and consist of long and slender teeth, some of which are very long, while the rest are somewhat shorter. They are finely streaked throughout their length, pointed like awls, and movable inwards, so that the long front teeth lie backwards, the side teeth inwards. All of them are covered with a jet-black skin, the extension of which cannot with certainty be determined in this specimen ; a few of the shorter teeth are still completely covered with it; but the points of long teeth have probably always been bare. The number of teeth in each half of the jaw is 7-9, to which 1886. ] NEW PEDICULATE FISH. 141 should be added one or more accessory teeth, which are quite short, and are situated immediately at the base of the longest teeth ; pro- bably these accessory teeth are meant to supplant the others when these are shed or lost, which may often happen when devouring the huge prey. In the intermaxillary, the longest teeth in front have a length of 6 millim., and are quite straight (on the left side it is not fully developed) ; the other teeth are shorter, not more than 3 millim. long. The total number of teeth in each intermaxillary is 8 or 9, to which must be added 2-3 accessory teeth situated at the base of the longest. In the lower jaw the two foremost teeth (and the 4th) are parti- cularly long, the others somewhat shorter. In each half jaw there are seven teeth, to which must be added the two accessory teeth situated at the base of the longest. The innermost tooth in the jaw is quite small. Of the two long front teeth, the first is somewhat shorter than the second, considerably curved ; its length is 4°5 millim. The second is the longest of all the teeth ; itis 8 millim. in length, and is also a little curved. It is placed a little inside of the row of other teeth, and has a short tooth at its base. The fourth has a length of 5 millim., and it also has an accessory tooth; the others are shorter. The upper pharyngeal bones have each a group of about six teeth forming two long irregular rows. The lower pharyngeals do not appear to have teeth. The vomer has a single tooth, which, like the pharyngeal teeth, is about the length of the shorter teeth in the jaws, and is slightly curved. Cephalic spine.—The first dorsal appears as a single tentacle on the forehead (the cephalic spine). Its basal element is not sub- cutaneous and procumbent, but erect and continuous with its distal part. When laid back its bulb reaches to the hind margin of the eyes, or just between the two orbital spines, in which position it fills up the concavity on the forehead. It is situated at the front margin of the snout. Its length is 10 millim., of which half comprises the peduncle, which is rather thick, especially towards its base, the other half the head, which forms an oblong bulb, the breadth of which is 3 millim., or about the same as the diameter of the eye. The bulb ends in a pair of exceedingly short and slender threads, which, in a good light, can be seen to have small papilla-shaped bodies on one side, of the same kind as the papille on the guttural tentacle, but much smaller (probably answering to the “scales” which, according to Liitken, cover the threads of the tentacles of the Himantolophoids). The colour of this cephalic spine is jet-black as far as the middle of the bulb; its other half is white (perhaps silvery in the living specimen), as in most or all the other species of the Ceratiidee. The jfins.—The second dorsal is situated far behind, close into the caudal fin, although separated from it by a distinct space. It has three single rays, which at their base are enveloped with a thick 142 PROF. COLLETT ON A NEW PEDICULATE FisH. [Mar. 2, skin, a continuation of that of the body. It is directed backwards, and the point of the fin extends a little beyond the root of the caudal fin (about an eye’s length). The anal fin is much like the second dorsal, and is placed right beneath it ; it has two rays, which also are single. The caudal fin consists of nine rays, four in the upper, five in the lower half. Of these the outermost are somewhat shorter than the middle ones; thus the fin is somewhat pointed. The four middle rays are bifid from below the centre; the others are simple. The ventral fins are wanting. The pectorals are small and rounded; the pseudobrachia very short. On the right side there are 14, on the left side 15 rays, most of which are simple, and only the middle ones seem to be bifid at the ends. The length of the pectoral (including the pseudobrachium) is only 5 millim., or the length of the bulb of the cephalic spine. The guttural tentacle is nearly 34 times as long as the tentacle on the snout (23 millim.), or has about the same length as the distance from the front of the eye to the root of the tail. It is placed on the throat, at a distance from the symphysis about equal to half the length of the jaw. It is thinner than the cephalic spine, and divides itself at the end into two short pointed blades, the length of each being 6 millim. Whilst the tentacle otherwise is black, the inner edges of these blades are white, like the upper half of the snout tentacle, and are furnished with a row of round papille, about 30 on each, resembling a chain of pearls. These small bodies undoubtedly have a use, either as organs of sense or as the source of the phosphorescent light *. The abdominal cavity is greatly distended, somewhat flattened un- derneath, which is in consequence of the position the swallowed fish has taken up. This fish, which undoubtedly is a Scopeloid, has a length of about 70 millim., and is therefore not far from being half a length longer than the specimen itself. It lies with the head and the caudal fin bent backwards and the belly turned down. Anus. Its position cannot be given with certainty. The skin is smooth throughout, and covers all the spines on the head as well as the teeth. Lateral line or mucous glands cannot be detected. The colour everywhere is jet-black, with the exception of the upper half of the bulb of the tentacle on the snout, and the inner margins of the ends of the guttural tentacle, which (in the preserved specimen) are white, but which in the living fish have probably been silvery and phosphorescent. The fin-rays are also black, the membrane blackish. The mouth is also black, as well as the covering of the teeth. * A similar phosphorescent guttural tentacle is mentioned in Hustomias obscurus, captured from enormous depths during the voyage of the ‘ Talisman ’ (‘La noun 1884, p. 184; Day, ‘Fishes of Great Britain and Iveland,’ p- xxvii). ps “HMHATIONT ANAYHAONIT dunt - s0ag ase TUT W377 Pp yuug Pp a | M Id 988l°'S'°Z/d 1886. | ON THE CHARACTERS OF RHINOCEROS SIMUS. 143 Affinities.—Linophryne lucifer belongs to the family: Ceratiida, and resembles Melanocetus johnsonii, Giinth. (Proc. Zool. Soc. 1864, p- 301) in several particulars, viz. that only one single spine in the first dorsal is developed (the nasal tentacle), in the enormous mouth, the almost square head, as well as in its small size, its black and smooth skin, and pendent abdominal cavity, besides in its having 2 pairs of gills and unarmed branchial arches; but it differs from this species by the formation of its teeth, the oblique mouth, its rudimentary gill-openings, its short and thick nasal tentacle, in the number of its fin-rays, the spiny armature of its head, and its comparatively well-developed eye. Tt differs from all the Ceratiide in its having a long guttural tentacle, also in the low number of rays in its second dorsal and anal fins. Locality.—A single specimen, with a total length of 49 millim., was caught by Capt. P. Andresen in May 1877 floating in the sea (about 36° north latitude, 20° west longitude) 3° N.W. of Madeira, and was presented to the Museum of the Christiania University. During several years it remained unnoticed in the private house of the late Director of the Museum, Prof. Esmark, but after his death it was returned to the Museum (December 1885). Mr. Andresen, who is now residing in Christiania, reports to me that on the day mentioned he was on a voyage to the West Indies. He was capturing turtle in his boat; there was a heavy sweil, but the water was smooth. After a time he caught sight of this little black fish, which lay on the surface quite alive, but almost motion- less, which was not surprising when it was discovered that it had just swallowed a fish longer than itself. It did not lie on its side, but was apparently unable to swim away. By getting the bailer under it, he lifted it out with ease, and in order to keep it fresh he gave up his search for turtle and rowed back to the ship, where it was placed in spirit for preservation. EXPLANATION OF PLATE XV. Fig. 1. Full view of Linophryne lucifer, 2. 2. Front view of head, showing open mouth. 3. Guttural tentacle, }. 2. Note on the External Characters of Rhinoceros simus. By P. L. Scuarer, M.A., F.R.S., Secretary to the Society. [Received February 24, 1886.] (Plate XVI.) The heads of the two African Rhinoceroses exhibited by Mr. E. Gerrard, Jun., at the last meeting of the Society, and again placed on the table this night by Mr. Gerrard’s kind permission, have 144 . ON THE CHARACTERS OF RHINOCEROS stmus. [Mar. 2, enabled me to make a comparison between Rhinoceros bicornis and Rhinoceros simus, which I have never before had an opportunity of doing. Indeed, as is well known, such specimens of the latter species, with the exception of a single immature example in the British Museum, are almost unknown in Europe. On looking at the two heads now before us side by side, the points by which this part of the two animals may be distinguished present themselves very appreciably. In the first place, as is already well known, the “ White” or ‘ Square-nosed”” Rhinoceros, as it is much better called, is distinguished by its short upper lip, which is quite apparent in the example now before us. In R. bicornis the central portion of the upper lip is far extended, and forms a quasi- prehensile organ. This is sufficiently manifest in the specimen now on the table, but is still better seen in the living example of the same animal in the Society’s Gardens. A second point in which the heads of the two African Rhinoceroses differ materially is in the size and shape of the ears. In R. bicornis (Plate XVI. fig. 2) the ear-conch is much rounded at its extremity and edged by a fringe of short black hairs which spring from the margin. In R. simus (Plate XVI. fig. 1) the ear-conch is appa- rently much more elongated and sharply pointed at its upper extremity ', where the hairs which clothe its margin constitute a slight tuft. While the upper portion of the ear-conch is much more expanded in #. simus than in R. bicornis, in the lower portion the two margins are united together for a much greater extent, and form a closed cylinder, which in the present specimen rises about 3 inches above the base. The total’ length of the ears in the present specimens is, in R. simus, 12°5 inches and in R. bicornis about 9°5 inches. A third point in which the two species appear to differ is in the shape of the nostrils, which, judging from the present specimens, are, in Lt. simus, elongated in a direction parallel with the mouth, while in R. bicornis they are more nearly of a circular shape. Again the eye in &. simus appears to be placed further back in the head than in R. bicornis. A regards the well-known differences in the skulls of these two Rhinoceroses, which are obvious enough on a glance at the specimens on the table, I will say nothing on the present occasion, but simply refer to De Blainville’s figures (Ostéographie, Rhinoceros, pl. iii. and iv.), and to Prof. Flower’s remarks on this subject in the ‘ Pro- ceedings’ of this Society for 1876 (p. 452). * This peculiar feature is well shown in the figures of R. simus given by Smith (Ill. S. Afr. Zool. Mamm. t, xix.), and Harris (Portraits, &e. pl. 19). PZ.S. 1886. Pl. XVI. Hanhact imp. DS OF RHINOCEROS SIMUS (Fig.1) AND R.BICORNTS. (Fig.2) 14 ph i 1886. ] ON THE AIR-SACS OF THE CASSOWARY. 145 3. Note on the Air-sacs of the Cassowary. By Franx E. Brepparp, M.A., F.R.S.E., Prosector to the Society. [Received March 1, 1886.] The following note refers to a male Casuarius uniappendiculatus which died in the Society’s Gardens on February 15th of the present year. Since no description of the respiratory organs of this bird has, so far as I know, been published, I have thought it worth while to bring a note upon the subject before the Society, to supplement Prof. Huxley’s paper upon the respiratory organs of Apéeryx' and Prof. W. N. Parker’s ‘ Note’ upon the same structures in Rhea *. As regards its air-sacs the Cassowary appears to resemble Apteryx much more closely than Rhea, though differing slightly from the former. In dpteryx the main difference in the air-sacs from those of Carinate Birds is in the small extent of the abdominal air-sac. “In Apteryx the whole of this sac is enclosed between the oblique septum and the pulmonary aponeurosis, the dissepiment between its loculus and that of the posterior intermediate sac being situated almost midway between the second dissepiment and the posterior extremity of the pneumatic chamber. In the Duck, on the con- trary, the dorsal end of this dissepiment~is attached close to the posterior extremity of the lung, and thence slopes very obliquely backwards. ‘The capacity of the posterior intermediate air-sac thus becomes greatly increased. But, as the capacity of the posterior air-sac is also vastly greater than in dpéeryz, its posterior wall has been, apparently, driven out, like a hernial sac, between the peri- toneum and the parietes, and projects into the abdominal cavity.” (Loe. cit. p. 566.) In Rhea “ the anterior and posterior intermediate and the posterior air-sacs are almost precisely similar to those of the Duck. The dorsal end of the dissepiment between the posterior intermediate and the posterior sac slopes backward; and the posterior wall of the latter has been, as Prof. Huxley describes it, ‘ apparently driven out like a hernial sac, between the peritoneum and the parietes’ projecting almost to the posterior end of the abdomen.” (Parker, loc. cit.) In Casuarius uniappendiculatus the anterior and posterior inter- mediate air-sacs are of about the same size and are separated from each other and from the posterior sac by erect, almost vertical dissepiments, which are entirely parallel with each other ; the dissepiment which separates the posterior air-sac from the one in front does not slope backwards any more than does the dissepiment in front of it. The posterior air-sac is entirely shut off from the abdominal cavity by the oblique septum ; there was no trace whatever of any prolongation of its walls among the coils of the intestines ; the whole of the sac, as in Apteryz, is enclosed between the oblique septum and the * P.Z.S. 1882, p. 560. ? P. Z. 8. 1883, p. 141. 146 ON THE AIR-SACS OF THE CASSOWARY. [Mar. 2, pulmonary aponeurosis. The shape of the posterior air-sac’ is, however, rather different from that of the corresponding air-sac in Apteryx. Inthe latter bird, according to Prof. Huxley’s figure (oc. cit. figs. 1 and 2, v.), the posterior air-sac is rather smaller than the preceding posterior intermediate air-sac, and does not extend further back than the lung. In Casuarius the posterior air-sac forms ante- riorly a rounded capacious cavity, which pretty nearly corresponds in size to that of the posterior intermediate sac ; the cavity is, however, prolonged for some way backwards as a narrow interspace between the oblique septum and the parietes, but this posterior region is altogether outside the abdominal cavity and does not in the least resemble the condition of the posterior air-sac which is characteristic of the Carinatee. The pulmonary aponeurosis is thick, and costo-pulmonary muscles arising from the ribs are spread out over its surface; the oblique septum itself is stout and thick. Each lobe of the liver is contained in a separate compartment as in so many other birds (see P.Z.S. 1885, p. 836); the gizzard is enveloped in a special coat of peritoneum, while the intestines are covered below by a stout horizontal septum which laterally becomes indistinguishably fused with the oblique septum; in this respect therefore the Cassowary agrees with the Emu and with many Carinatee. Between the horizontal septum and the ventral peri- toneum wasa large mass of fat. The special resemblance between Casuarius and Apteryzx in the structure of the respiratory organs is not altogether in accord with the results obtained from the study of the structure of other organs. Prof. Garrod ! divides the Struthiones into three families, Apterya being the type of one ; Casuarius and Dromeus, Struthio and Rhea form the two other families. A study of the osteology has led Prof. Mivart® to a similar conclusion. The results contained in the present Note confirm the opinion expressed by these two authors that Casuarius and Rhea should be separated. I have not had the opportunity of examing the air-sacs of the Ostrich, but, judging from a sketch left by the late W. A. Forbes, they appear to be like those of Rhea. In Dromeus the air-sacs are not similar to those of Casuarius, but agree with Rhea in the extension of the posterior air-sac into the abdominal cavity. At the end of his paper *‘ On the Axial Skeleton of the Struthionide ” Prof. Mivart represents the affinities of the Struthious birds in a phylogenetic scheme. Removing Dromeus from Casuarius and placing it nearer to Rhea and Struthio, that scheme will exactly represent the position of the different genera of Struthiones as indicated by the structure of their respiratory organs. * Coll. Papers, p. 219. ? Trans. Zool. Soc, vol. x. p. 21. 1886.] ON THE SYRINX ETC. OF CAPRIMULGID. 147 4, On the Syrinx and other Points in the Anatomy of the Caprimulgide. By Franx E. Bepparp, M.A., F.R.S.E., Prosector to the Society. [Received March 1, 1886.] It has been known for a long time, and the fact is recorded in most text-books of comparative anatomy’, that Steatornis among the Caprimulgidz and Crotophaga among the Cuculide are distinguished from the other genera of their respective families, as well as from all other birds, by the possession of a bronchial syrinx. The voice-organ of these two birds, instead of being situated at the junction of the trachea with the bronchi, as in the vast majority, or being formed by a modification of the lower portion of the trachea, as in the tracheo- phone Passeres, is produced by a modification of certain of the bron- chial rings some way from the bifurcation of the bronchi. The structure of the syrinx of the Guacharo was first made known by Johannes Miiller*, and subsequently described and figured by Garrod’. I am unacquainted with any exact description of the syrinx of Croto- phaga, which, as I have myself indicated*, presents the following resemblances to, and differences from, the syrinx of Steatornis. In both types the bifurcation of the trachea to form the bronchi takes place precisely as it does in the Mammalia ;- that is to say, the ante- rior bronchial rings are complete rings, and in no way different from the rings of the trachea. The membrana tympaniformis does not com- mence until about the tenth (Crotophaga) or thirteenth (Steatornis) bronchial rings; at this point the rings not only cease to be complete rings but alter in their character, being narrower and softer than the anterior bronchial rings, and separated from each other by wider inter- vals of fibrous tissue; the single intrinsic muscle is inserted on to the first of these modified bronchial rings ; the last two or three rings before that on which the muscle is inserted are semirings, the mem- branous intervals between their inner extremities, which constitute the upper part of the membrana tympaniformis, becoming gradually less and less, until it disappears entirely and the rings are complete rings. These, however, although they support the anterior part of the mem- brana tympaniformis, agree in their structure with the tracheal and anterior bronchial rings; like them they are placed close together and ossified ; there is no transition between the anterior and posterior bronchial semirings ; their character abruptly changes at the semiring on to which the intrinsic muscle is attached. In Cvofophaga the menbrana tympaniformis extends back unto the entrance of the bronchus into the lung ; in Séeatornis the membrana tympaniformis 1 Huxley, ‘The Anatomy of Vertebrated Animals,’ London, 1871, p. 315; Gegenbaur's * Comparative Anatomy,’ French Trans. by O. Vogt, p. 776. * Bericht d. Akad. Wiss. Berlin, 1841, p. 172; Mill. Arch. 1842, pu; Stimmorg. d. Passerinen, Berlin, 1847, p. 9. . 3 Coll. Papers, p. 188. 4 P.Z.8. 1885, p. 173. 148 MR. F. E. BEDDARD ON THE SYRINX AND OTHER [Mar. 2, is of less extent, and there is an interval between it and the lung occupied by complete bronchial rings. In the paper referred to I have described the syringes of other genera of the Cuculide: in some genera (e.g. Cuculus) the syrinx is tracheo-bronchial; in others (e.g. Centropus) the syrinx presents a very close approximation in its structure to the bronchial syrinx of Crotophaga. In these Cuckoos the intrinsic muscles of the syrinx are, as in Crotophaga, attached a long way down the bronchus, but the bronchial rings anterior to the attachment of these muscles are not complete rings as in Crotophaga, but are very nearly so, inasmuch as their free extremities are separated by a very short extent of mem- brane, which widens out below the attachment of the syringeal muscles to form the membrana tympaniformis; there is, moreover, a similar change in the nature of the bronchial semirings at the point where the syringeal muscles are inserted. In the Caprimulgide there is a variation in the structure of the syrinx which is closely parallel to that of the Cuculide. Three types of syrinx can be recognized in this group, in the genera which I have myself been able to examine, which are: Caprimulgus. Batrachostomus. Chordeiles. Podargus. Nyctidromus. Steatornis. Aigotheles. In the first four genera the syrinx is tracheo-bronchial ; in Batra- chostomus and Podargus the syrinx approximates in structure to the purely bronchial syrinx of Steatornis. I need not redescribe the syringes of Caprimulgus and Chordeiles, which are already known from the investigations of Cuvier, Nitzsch, and Audubon. The remaining genus which possesses a tracheo- branchial syrinx, viz. Nyctidromus, has not, I believe, been described. In Nyetidromus (fig. 1) the syrinx is not widely dissimilar from that of Caprimulgus. The tracheal rings are separated mesially, both on the anterior and posterior aspect, by considerable membra- nous intervals; the last four are, however, closely applied, as shown in the accompanying drawing (fig. 1), which represents the syrinx viewed from in front; the terminal rings of the trachea are much more slender than the bronchial semirings, and the last appears to be defective laterally, or is covered by the succeeding first bron- chial semiring. The last two rings of the trachea, as well as the first five bronchial semirings, are ossified; the ossification has also extended on to the sixth bronchial semiring and the antepenultimate tracheal ring. The intrinsic muscles are attached on to the first bronchial semiring. Posteriorly is a rhomboidal ossified plate, to which the pessulus is attached ; it represents the middle portion of the last four or five tracheal rings, but is separated from them com- pletely. The syrinx of Zgotheles is displayed in the accompanying drawing (fig. 2). The syringeal muscles are inserted on to the third bron- 1886.] POINTS IN THE ANATOMY OF CAPRIMULGIDE. 149 chial semiring, which differs from the two preceding in being more slender; the two first bronchial semirings are stout and closely applied. The terminal ring of the trachea is pointed downwards anteriorly, as shown in the figure; posteriorly it is incomplete ; the penultimate, antepenultimate, and the next tracheal rings are Fig. 1. Syrinx of Nyctidromus albicollis. Fig. 2. Syrinx of Agotheles nove-hollandie. separate anteriorly, but posteriorly are fused for a short space in the middle line, and are continuous with the pessulus, which arises ante- riorly from the last tracheal ring. Batrachostomus.—I am indebted to the kindness of Mr. R. Bowdler 150 MR. ¥F.E. BEDDARD ON THE SYRINX AND OTHER [Mar. 2, Sharpe for the opportunity of examining a syrinx of this bird. The accompanying drawing (fig. 3) illustrates the syrinx as seen from behind. The last ring of the trachea is complete in front and incomplete behind. The intrinsic muscles are attached to the middle of the sixth bronchial semiring, though, when viewed from behind, it would appear that the seventh bronchial semiring served for the attachment of these muscles ; this appearance is caused by the incomplete terminal tra- cheal ring. The six anterior bronchial semirings are ossified and firmly united to each other and to the trachea; both the anterior and poste- rior extremities of the successive semirings are united by a continuous bar of cartilage. The remaining bronchial semirings differ to a very Fig. 3. Syrinx of Batrachostomus. marked degree from the anterior ones ; they are slender and unossified, and separated by widish membranous intervals; there are about ten of these rings in either bronchus. The membrana tympaniformis, which unites together the opposite sides of each bronchus, forming its inner wall, is of equal diameter both in the posterior and anterior regions of the bronchus; there is a marked constriction, however, at the point which divides the anterior from the posterior region of the bronchus. Podargus cuvieri.—The syrinx of this Goatsucker appears to be formed upon the same type as that of Batrachostomus, and to show the same characters even to a greater degree. I have not been able to examine the organ itself; the following remarks are based upon a sketch made by the late Prof. Garrod’. ! There is a brief description, unaccompanied by any figure, in Stannius’ ‘Lehrbuch der Vergleichenden Anatomie,’ Bd. ii. p. 321. 1886.] POINTS IN THE ANATOMY OF CAPRIMULGIDZ. 151 The intrinsic muscles of the syrinx are inserted on to the fifteenth or sixteenth bronchial ring, much lower down therefore than in Batrachostomus; the first two bronchial rings are complete; the following fourteen are semirings, but are wide, firmly united to each other, and ossified ; the membrana tympaniformis forms the inner wall of this and of the following section of the bronchus. The posterior section of each bronchus, as in Batrachostomus, is formed of slender cartilaginous semirings separated by wide membranous intervals. As far as the structure of the syrinx is concerned Steatornis stands alone; Podaryus and Batrachostomus are closely similar to each other, and are transitional between such genera as Caprimulgus and Steatornis ; the insertion of the intrinsic muscles so far down the bronchus, and the similarity between the anterior rings of the bron- chus and those of the trachea, is evidently an approach in structure to the bronchial syrinx of Steatornis. gotheles resembles Batra- chostomus more closely than it does Caprimulgus, but the number of bronchial semirings which intervene between the trachea and the insertion of the syringeal muscles is still further reduced. Capri- mulgus, Chordeiles, and Nyctidromus are very closely allied in the structure of their syrinx, which is tracheo-bronchial, and shows no approach to the bronchial syrinx of Steatornis, as do the syringes of Podargus, Batrachostomus, and (to a very much less extent) dgo- theles. The arrangement of the genera of Caprimulgide, as indicated above by the structure of their syrinx, is, I believe, in accord with the opinion of most ornithologists. With regard to other structural characters, the foliowing notes upon certain of the viscera and muscles appear to be worth recording. Visceral Anatomy. The intestines of the Caprimulgide are furnished with ceca, with the exception of those of gotheles. Mr. Forbes has left a MS. note to this effect, and I cannot find any trace of ceca in the spirit- preserved specimen of the last-mentioned form. In all the genera the left lobe of the liver is rather the smaller, and a gall-bladder is present save in Chordeiles’. The air-sacs in one specimen of Steatornis were rather peculiar in structure. The pcints in which they were found to differ from other birds are in the posterior intermediate air-sac. This sac on both sides of the body is considerably larger than the preceding anterior intermediate sac, and is furnished with two principal ostia placed near to the external border of the lung. These: pertures have a different position in relation to each other on either side of the body ; in the right lung these apertures do not both open into the posterior intermediate air-sac as they do on the left side of the body ; the most anterior of the two ostia opens into a small wedge-shaped atr- cell, which is completely separated by septa both from the posterior 2 Garrod MS. 152 MR. F. E, BEDDARD ON THE SYRINX AND OTHER [ Mar. 2, and anterior air-sacs ; towards the median line, however, its limiting septa coalesce, and here the anterior and posterior intermediate air- sacs follow each other directly ; this supplementary air-sac therefore is placed upon the outer margin of the lung and does not extend to the middle line. The other specimen of Steatornis unfortunately had the lungs destroyed, so that I cannot positively state whether the above-described peculiarity is merely a variation or characteristic of the bird, though on one side there were certainly two ostia to the posterior intermediate sac. Myology. The disposition of the tensores patagii varies characteristically in the different genera. In Caprimulgus, Nyctidromus, and Chordeiles there is a biceps-slip, which is absent in Steatornis, Podargus, and 4Egotheles. Prof. Garrod has figured the patagial muscles of Steat- ornis (loc. cit.), and I find them to be exactly similar in Podargus. Aigotheles is a little different from either of these genera; there is no anterior branch to the tendon, or only just a trace of one, close to the insertion on to the extensor muscle. In Caprimulgus, Chordeiles, and WVyctidromus there is an absolute similarity in respect of these muscles; since Caprimulgus has been already figured by Garrod (Joc. cit. p. 185), there is no necessity to illustrate the two remaining genera, as it would be merely a repetition of his figure. ; A peculiarity in the myology of Steatornis is not referred to by Prof. Garrod in his account of the anatomy of that species; that is the presence of an expansor secundariorum. In a later paper, where a list is given of those families that are characterized by having an expansor secundariorum muscle, he states that the Coractidee are the only Anomalogonatous birds which are thus provided. In the speci- men of Steatornis before me there is a well-developed expansor secundariorum arising in the usual way and attached to the ¢eres near to its insertion. The termination of the expansor secundariorum in Steatornis is therefore similar to that which has been recorded by Garrod in Ortyx, Numida, &e. Since noting this fact I see that Mr. Forbes’ has already mentioned it. The diceps muscle is split about halfway down into two distinct tendons of insertion, which are severally attached to the radius and ulna. In Podargus, Zgotheles, and Nyctidromus the biceps is similarly divided into two, the division passing for a certain distance into the substance of the muscle itself, and not being merely restricted to its tendon of attachment. This structural feature is not peculiar to the Caprimulgidze, but is found in other families of birds. In all the Caprimulgidee that I have dissected, the anconeus longus has a tendinous humeral head. , The peroneal muscles vary in the different genera of Caprimulgide : in Steatornis and digotheles only the peroneus brevis is present ; in Podargus both peroneals are present with the usual attachments ; in Myctidromus 1 could only find the peroneus longus. ' Coll. Papers, p. 346. 1886.] POINTS IN THE ANATOMY OF THE CAPRIMULGIDE. 153 Dr. Gadow, in Bronn’s ‘ Thierreichs’ (Bd. vi. Abth. iv. p. 177), has referred to the double condition of the tendon of the tibialis anticus in Podargus ; this statement I am able to confirm from my own dis- section of that bird; but in the other genera this muscle has a more normal arrangement, being undivided at its extremity. The only other birds in which I have found a similar disposition of the tibialis anticus are the Owls (Strix pratincola); but Dr. Gadow has men- tioned Ohrysotis as another instance. Steatornis differs from the other genera in having no femoro- caudal muscle ; in the remaining genera the formula on Garrod’s system is AXY’. Steatornis therefore agrees with Podargus and Aigotheles in the absence of a biceps slip to the patagium; while those genera which agree with each other in the possession of a tracheo-bronchial syrinx, viz. Caprimulgus, Nyctidromus, and Chordeiles, have a biceps slip ; Steatornis is peculiar in the absence of the femoro-caudal muscle, and in the presence of an expansor secundariorum ; while go- theles appears to differ from its allies in having no ceca, and also in the structure of the patagial tendons. I am unfortunately unable to give any account of the visceral anatomy and myology of Batrachostomus, which I should imagine will be found to agree pretty closely with Podargus. All these facts lend additional confirmation to the generally accepted view that Steatornis is a peculiar type of Goatsucker and needs a special subfamily to itself. It evidently, however, comes nearest to Podargus, Batrachostomus, and gotheles ; and the fact that all these genera lay white eggs* is so far confirmatory of the anatomical resemblances; in the other Goatsuckers the eggs are coloured. A second subfamily will include Podargus and Batracho- stomus, while 4gotheles ought perhaps to be regarded as the type of a third subfamily. The remaining genera, Caprimulgus, Chor- deiles, and Nyctidromus, belong to the fourth subfamily. The Steatornithine are at one extreme, and the Caprimulgine at the other; Podargus, Batrachostomus, and digotheles are much nearer to Steatornis than to Oaprimulgus, but should be placed in an intermediate position. This view of the affinities of the different genera of Caprimulgidee almost entirely bears out the scheme of classification proposed by Mr. Sclater (Joc. cit.). 1 Coll. Papers, p. 346. 2 Cf. P. L. Sclater, P. Z.8. 1866, p. 127. Proc. Zoou. Soc.—1886, No. XI. 1l 154 REV. H. S, GORHAM ON NEW COLEOPTERA. [Mar. 16, March 16, 1886. Prof. W. H. Flower, LL.D., F.R.S., President, in the Chair. Mr. F. D. Godman, F.R.S., exhibited a series of examples of a Butterfly, Danais plexippus, from various localities, and made remarks on its distribution, which seemed to be gradually extending itself all over the world. Professor Bell stated that the species of Balanoglossus, an imperfect example of which he had exhibited to the Society on November the 17th of last year, had been described and named by M. R. Koehler, who had called it B. sarniensis’ ; the specimen on which his descrip- tion was based had also come from the island of Herm. Since the read- ing of that description, M. G. Pouchet * had reported to the Academy of Sciences that the species in question had been found at various localities on the northern and north-western coasts of France. The following papers were read :— 1. On new Genera and Species of Endomychide. By the Rev. H. 8. Gorsam, F.ZS., F.E.S. {Received March 5, 1886. | (Plate XVII.) The object of the following descriptions is to make known several most interesting and beautiful Coleoptera of the family Endomychide from various sources, but which are chiefly due to Mr. George Lewis’s collections made in Ceylon in 1882-3. A portion, however, are species that have been long known to me, as they are based on specimens collected by Mr. Bates on the Amazons. Of these there were mostly but one or two of each species, and it would no doubt have been satisfactory to have seen more examples ; of this, however, there seems but slender hope, while if left undescribed the specimens are practically lost. Two or three most interesting species, forming a new genus, are from examples in Mr. Cowan’s Madagascar collec- tion ; for the opportunity of describing these my thanks are due to Dr. Sharp. SPATHOMELES. 1. SPATHOMELES INFLATUS. (Plate XVII. fig. 5.) Oblongus, niger, nitidus ; elytris piceo-purpurascentibus, marginibus nigris, humeris calloso-inflatis. Long. 10 millim. 92? Hab. Ceylon. Head, antennze, legs, prothorax, and underside shining black. ' Comptes Rendus, cii. (25 Jan. 1886) p. 224. 2. es pnata: 1886.] REV. H. S. GORHAM ON NEW COLEOPTERA. 155 Head with a few scattered but distinct punctures; club of the antennee rather lax and dull. Thorax shining, not punctured, but with the surface uneven; anterior margin deeply excavated for the head, and with the anterior angles turned inwards; the sides much rounded in front; the disk with a short central elongate impression, and a round one on each side; the sides much puckered. Elytra smooth and waxy, impunctate ; all the disk of a pitchy-purple tint, which in life was, as Mr. Lewis informs me, of a most beautiful violaceous colour. They have a double, not much elevated, tumidity each side of the scutellum. The humeral callus is much inflated, to the extent of about a quarter of the length of the elytra; this tumidity is scarcely carinate and not spinose; the reflexed margin of the elytra is complete, running as a fine line beneath the callus up to the basal angle; the epipleural fold is black and shining. The anterior tibize are very faintly incurved, and compressed into a shallow spoon-shaped hollow at their apices, and the middle pair are more strongly incurved at their tips, the hind pair slightly so; all the tibie have the apices pubescent inwardly; the hair at the tips is golden. Of this very singular and beautiful Spathomeles a pair were beaten off a dead branch in the jungle by Mr. Lewis at Dickoya, at 5000 feet elevation. 2. SPATHOMELES ORNATUS. S. decorato valde affinis, oblongus, niger, nitidus; elytris sub- violaceis, maculis tribus elevatis, una basilari rotundata, una ante medium transversa in medio constricta, una subapicali sub- lunulata, luteis. Long. 13-15 millim. ¢ @. Mas. Zlytris spina dorsali brevi obtusa, femoribus anticis, tibiis mediis ante apicem dentatis, tibiis posticis ante medium angu- lariter late dentatis. Hab. Assam. Very closely allied to S. decoratus, Gerst., and perhaps not more than a geographical form; the evident toothing of the hind tibiz is, however, very important, and the union of the two middle yellow spots, which in S. decoratus are, so far as I have observed, always separate, seems to point to a permanent specific difference. The spots are all rather more developed than in S. decoratus ; the basal one is round. One male and two female specimens. STICTOMELA, gen. nov. Corpus ovatum. Elytris convexis, maris haud spinulosis. Pro- thorax antice ampliato-rotundus. Prosternum apice truncatum, coxas anticas superans. Mandibule apice bidentate. Palpi mazillares articulo ultimo conoideo apice minute truncato. A genus very nearly approaching Spathomeles; the points in which it principally differs are, that in the males the elytra are not armed with a spine, and the prothorax is differently shaped, resem- bling more that of the Amphisterni of the second aceon without 11 156 REV. H. S. GORHAM ON NEW COLEOPTERA. [ Mar. 16, spines. The apex of the prosternum is not so widely rounded but sub- mucronate. The apex of the jaws is notched, much as in EZncymon and Hngonius, the teeth being of equal length and the exterior one not bifid. The front tibiz of the males have a very small tooth near their apex. Engonius, to which this genus approaches in some of its characters, has the apex of the elytra obliquely truncate, so that they are open at the sutural angle; in the present genus the elytra are together uniformly rounded. 1. SticTOMELA CHRYSOMELOIDES. (Plate XVII. fig. 6.) Oblonga, elytris apice equaliter rotundatis, nigro-enea, nitida ; capite prothoraceque inequalibus, crebre sat fortiter punctatis, hoc profunde canaliculato ; elytris crebrius subtiliter punctatis, perobsolete subsulcatis, callo humerali modice elevato, obtuse carinato, punctisque quatuor aurantiacis, duobus basalibus, duobus subapicalibus, oblique positis. Long. 9 millim. 3 9. Mas. Tibiis anticis ad apicem intus excisis, intermediis leviter cur- _ vatis, apice mucronatis. Hab. Dickoya, Ceylon. Head brassy black, a little shining ; epistoma thickly and strongly punctured, posterior part less thickly ; antennee as in Spathomeles, but the club rather lax, apical joint obliquely compressed at the tips. Thorax with the surface shining but uneven, the principal impression being a central channel with a punctiform pit on each side in the middle, a basal transverse line, and the ordinary basal sulci; the sides are, however, wrinkled; the lateral margins are much rounded in front, and the front margin rather deeply excavated and bisinuate, the front angles being acute. The humeral callus is raised into a blunt carina, terminating in the external one of two basal, orange, round spots; the two apical ones are placed somewhat obliquely, that nearest the suture being furthest from the apex, and oblong but irregular in shape. The femora are clavate and distinctly punctured ; the tibiz are bent a little in both sexes, but more strongly so in the male, and in that sex terminate inwardly in a short mucro; they are pubescent at the tips. The tarsi and claws are pitchy, clothed with golden pile beneath. The intercoxal plate of the basal ventral seg- ment is sparsely but deeply punctate. Four specimens, three males and one female, of this beautiful species were captured by Mr. Lewis. 2. STICTOMELA OPULENTA. Oblonga, nitida, nigra ; elytris confertim crebrius punctatis, singulis maculis sex rubris, tribus basalibus, tribus subapicalibus irregu- laribus, quasi fasciam formantibus. Long. 10 millim. 6. Mas. Tibiis anticis dente parvo adjacente, juxta apicem infra dentem excisis ; segmento apicali ventrali, tuberculo instructo. Hab. Ceylon. Head strongly and deeply punctured, the epistoma especially so, with fewer and more scattered punctures; antennee as in Engonius, but with the club a little more lax. Thorax uneven but shining, 1886.] REV. H. S. GORHAM ON NEW COLEOPTERA. 157 with a marginal line round the entire edge uniting with the central channel in front ; front margin deeply bisinuate ; sides hardly so much rounded in front asin S. chrysomeloides. Elytra longer than in that species, thickly and distinctly punctured, hardly any trace of sulcation or striation ; shoulders with a callus well raised, ending in a deep red spot, another spot near the scutellum, and a third between these two ; posteriorly are two small oblong spots (united in the specimen described) near the suture about one third from the apex, and another between these and the margin. There is a fine sutural stria for the whole length of the elytra, and the margin is narrowly reflexed. Legs and underside shining black ; femora punctate, but more finely than in S. chrysomeloides; anterior pair in the male compressed at the tip and with a very small fine calear above the spatulate compression. The tubercle on the apical ventral segment is squarish and impressed on its top so as to seem faintly bidentate. A single male specimen is all that Mr. Lewis secured of this species. CyMOoNES. Characteres plerumque ut in genere Encymon ; differt mesosterno haud transverso, prothoracis basi medio vix marginato, sulco transverso nullo, antennarum clava elongata, laze articulata, articulis nono et decimo viz latioribus, maris tibiarum anticarum dente lato. I have no doubt that the species for which I propose this new genus is the Madagascar representative of Encymon, with which it is associated in the form of the mandibles. It has, however, a different facies, principally owing to the form of the pronotum, which is more convex, with its margins even and scarcely at all reflexed. The longitudinal basal sulci are present, but the transverse one is quite obsolete. The mode of toothing of the front tibia of the male is, moreover, quite different to that of Encymon; in the only species of that genus in which I have seen it take place, and which is figured by me (Endom. Recitati, tab. f. 10), the tooth is small and close to the apex ; here it is wide and strong and near the middle of the tibia. 1. Cymones sHarpi. (Plate XVII. fig. 4.) Piceus ; prothorace elytrorumque apicibus flavis, illo guttis duabus magnis oblongis, punctisque tribus parvis nigris, capite femori- busque saturutius nigro-piceis ; trochanteribus, femoribus basi, tibiis tarsisque ferrugineo-flavis. Long. 9 millim. 6. Mas. Tibiis anticis dente basi latissimo, apice acuto infra medium, tibiis intermediis et posticis apice leviter incurvatis. Hab. Madagascar, Betsileo (Cowan). Head black, mouth and palpi testaceous, epistoma with a few indistinct punctures, crown smooth, antennal orbits raised. Antenne piceous, rufo-piceous at the base; the proportion of the joints as in Hncymon till the ninth, which with the tenth and apical joints are elongate, only rather longer and more widened at their tips than ad 158 REV. H.S. GORHAM ON NEW COLEOPTERA. [Matr. 16, those preceding them. Thorax about as long as wide if the projecting front angles are taken in, widest a little below the front ; basal angles right angles, sides a little sinuate not angular, front margin rounded and a little prominent, basal margin nearly straight ; on the disk, which is very even and smooth, are two large inky-black oblong marks a little obliquely placed, a small dot on each side where the thorax is widest, and one in the middle, near the base. Elytra pitchy, inclining to brown, the apex is yellow, and this colour returns some way up the suture and the margins ; they are convex, evenly ovate, and rounded at the apex, narrower at the base, and with a very obsolete sutural stria and scarcely at all widened margin; the epipleural fold is yellow. There is no visible punctuation on their surface ; but it is not glabrous as in Encymon angulatus, but very finely alutaceous, though the sculpture is hardly visible at all. Only two specimens of this insect have come under my notice ; both are males. One is in Mr. Lewis’s collection, and the other in Dr. Sharp’s, by whom they were obtained from Mr. Cowan. 2. Cymones cowani. (Plate XVII. fig. 1.) Nigro-subviolaceus ; capite, prothorace, antennis (clava excepta) pedibusque rufis, abdomine rufo-piceo. Long. 63 millim. 3 Q. Mas. Tibiis anticis dente acuto distantemediano, apicibus intermediis etiam leviter incurvatis. Hab. Madagascar (Cowan). More parallel than C. sharpi, and with the thorax not so convex above, and more quadrate, smaller, and differently coloured. The head and thorax are rusty red, very little shining, and without punctuation; palpi red ; antennze of moderate length, and with the club, which is black, abrupt, and with its two first joints transversely heart-shaped. The thorax is transversely quadrate, with the front angles a little prominent, the sides a little sinuate, nearly straight, base obsoletely margined, and the sulcidistinct but not deep. Elytra dark blackish purple, their apex ferruginous, slightly shining but not bright. Legs in the male example pitchy, in the female clear rusty red. Although this species and the following one differ in several particulars of their structure from C. sharpi, I have not been able to find any characters of sufficient importance to warrant their separation generically. In the abruptly formed club of the antennze and in the form of the thorax these two species are nearer to Encymon, but the strongly toothed tibiz in the male, and the form of the body, less swollen, and with its sides more parallel than in any eastern species of that genus, indicate a radical divergence from that type. Only two specimens have come under my notice; they were obligingly placed in my hands by Dr. Sharp for description. 3. CyMONES HELOPIOIDES. (Plate XVII. fig. 3, ¢.) Niger ; parum nitidus ; prothorace transversim quadrato, cum elytris subopacis. Long. 64-7 millim. 3S. 1886. ] REV. H. S. GORHAM ON NEW COLEOPTERA. 159 Mas. Tibiis anticis dente acuto, adjacente, infra medium ; intermediis apice incurvato, posticis leviter sinuatis. Hab, Madagascar (Cowan). Entirely black, subopaque above, body beneath shining. Antenne rather short, a little longer in the male than in the female, their club not very wide nor abrupt; head rather uneven, with a few seattered obsolete punctures. Thorax half as wide again as long, opaque ; punctuation very obsolete, minute and scarcely visible, basal sulci distinct ; front angles very little produced, scarcely at all in the female, sides nearly straight, base finely margined. Elytra half as wide again as the thorax and slightly widened behind, callus only faintly raised. The male specimen has two minute red dots near the apex of the elytra, in the female they are wanting. Meta- sternum (in male) depressed between the hind coxe, and first ven- tral segment with scattered small punctures. Two specimens from Dr. Sharp’s collection. AnrprytTvs, Gerst. 1. ANIDRYTUS QUADRIPUNCTATUS. Oblongus, parum ovatus, rufo-piceus, nitidus, crebre subobsolete punctatus, cupreo-pubescens ; antennis nigris, articulis quatuor basalibus et apice summo rufis; prothorace punctis quatuor discoidalibus nigris. Long. 8 millim. 2. Hab. Brazil, Blumenau. Head finely punctured, a little rugulose between the eyes; basal and three following joints of the antennz pale ferruginous, the fourth joint being deeper in colour, and at its articulation with the third nearly black. Thorax just twice as long as wide, from the front angles the sides are very evenly rounded to near the base, where they become straight. The basal furrows are two distinctly impressed, converging, linear channels; within them, where they end on the front of the disk, halfway between the base and the front margins, are two round black points (as in A. bipunctatus) ; more in front and more widely apart are two other black points. The disk and sides of the thorax are evenly, thickly, not confluently punctured, but the surface of the black spots is smooth, or in the external spots with one or two punctures only. The elytra are somewhat parallel, not strongly convex, evenly and more thickly punctured ; the punc- tures are (as is usual where they give rise to hairs) not pricked in, but irregular, somewhat linear, and flat-bottomed. Legs clear red, only a very little darkened at the base of the tibize. The underside wholly ferruginous red. Although this appears to be a species very nearly allied to A, bipunctatus, Gerst. (a species also from Brazil), the description given above will show that it differs not only by the four black spots of the thorax, but by the colour of the underside and legs as well. I have only seen one specimen, a female, which was sent to me by Herr Reitter, with other Coleoptera collected in the same district, 160 REV. H.S. GORHAM ON NEW COLEOPTERA. [ Mar. 16 2. ANIDRYTUS LIQUEFACTUS, Gorh. Endom. Rec. p. 47. I have received specimens of both sexes of what I consider identical with this species, of which the type is now in Mr. Lewis’s possession from Peru, and one male from New Granada (?) ; but these have only three joints at the base of the antenne red, and the apical joint is quite black. The size is from 73-83 millim. 3. AnIpRyTUS HUMILIS, Gorh. Endom. Ree. p. 48. Further specimens were taken by Mr. Belt at Chontales, Nicaragua, and will be noticed in the ‘ Biologia Centr.-Amer.’ in due course. EPoprrteRvs. 1. Epopterus EGANus. (Plate XVII. fig. 9.) Ovatus, rufo-brunneus, nitidus ; antennis nigris, articulis tribus basalibus testaceis; elytris singulis maculis tribus sat magnis eburneo-albidis nigro-cinctis, duabus basalibus oblique sitis, una subapicali. Long. 5-53 millim. 3 Q. Mas. ibiis anticis leviter curvatis, ad apices compressis. Hab. Amazon, Ega (H. W. Bates). Head and thorax rather pale castaneous red, not perceptibly punctured, very finely and very sparsely pubescent at the sides of the latter, narrowed to the front angles, and very narrowly margined ; basal sulci short, linear. Scutellum black. Elytra wider than the thorax, commencing to widen from the base to about one third from the base, whence they are evenly and ovally contracted to the apex ; each with three large yellowish-white spots edged with black. The underside is brownish red, the tibiee darker at their bases than the rest of the leg, as are also (but only very finely) the inner epipleural margins of the elytra. Two examples from Mr. Bates’s collection are now in Mr. Lewis’s. 2. EpopTeRvs EPHIPPIGER. (Plate XVII. fig. 8.) Ovatus, rufo-piceus, nitidus ; elytris flavis macula magna discoidali communi nigra; antennis nigris, articulis tribus basalibus flavis ; prothorace crebre, elytris parcius leviter punctatis. Long. 6 millim. 3. Mas. Tibiis anticis ad apices interne compressis, leviter incurvatis. Hab. Amazon (H. W. Bates). Nearly of the same oval form and of the size of EH. eganus, but distinctly punctured. Head red, nearly smooth; thorax twice as wide as long, not so wide as the elytra at their base, thickly and distinctly punctured ; basal sulci straight, a little converging, sides narrowing, slightly curved, margin distinct and faintly raised. Seutellum rufous, punctured. Elytra paler yellow than the thorax, punctures distinct, only a few scattered hairs at the sides ; epipleurze yellow, only very narrowly darker at their margins. Underside and legs uniformly pitchy red. I have only seen one example of this species, a male. It is very distinct from any Epopterus yet described. 1886.] REV. H.S. GORHAM ON NEW COLEOPTERA. 161 3. Epoprervs LINEOGUTTATUS. (Plate XVII. fig. 7.) Ovatus, rufo-piceus, nitidus ; elytris pallide flavis,sutura margin ibus- que lateralibus piceis, puncto humerali, lineolisque septem in singulis, 3, 3, 1, saturate piceis ; antennis nigris, articulis tribus basalibus rufis. Long. 6 millim. 3. Mas. Tibiis anticis interne sat fortiter incurvatis, ad apicem com- pressis. Hab. Amazon (H. W. Bates). Head, thorax, underside, and margins of the elytra rather light pitchy red ; punctuation of the thorax and elytra as in Z. ephippiger, distinct. The curious marking of the elytra consists of a humeral small dot, two elongate dashes near the suture, two shorter ones in the middle of the disk, two still smaller near the margin above the middle, and one small one near the apex. These dashes are not placed regularly, but the three near the base form a sort of fascia, as do the three below the middle. The scutellum is pitchy black. One small example. Sau, Gerst. 1. SauLa niGRIPEs, Gerst. Mon. p. 224,.t. 3. f. 2. Several specimens met with by Mr. Lewis, two of which were found in copula, present no appreciable distinction between the sexes. STENOTARSUS. 1. SteNnoTaRsus VALLATUs, Gerst. Mon. p. 342. Four specimens which I identify with this species were obtained by Mr. Lewis in Ceylon at Dickoya. The antenne are clear red; the series of punctures are more regular and not so coarse as in S. russatus. 2. STENOTARSUS RUsSATUs, Gorh. Trans. Ent. Soc. 1874, p- 446. One specimen met with by Mr. Lewis fully confirms my opinion as to the distinctness of this species, and I would only remark, in addition to the characters already given, that the raised thoracic margin has its surface distinctly flat in both species, indeed the edges of this margin are themselves raised, so that concave is the correct term. The dark, stout, and gradually thickened antenne will easily prevent this being confounded with S. vallatus. 3. STENOTARSUS SICARIUS. Ater, valde convexus, pubescens ; elytris basi thorace latioribus, distincte punctato-striatis ; thoracis margine laterali deplanato, haud bene elevato, antrorsum subito latiore. Long. 3 millim. Hab. Ceylon (Lewis). At once distinguished from any other Stenotarsus known to me by its entirely black colour. It is allied to S. vallatus and 8S. rus- satus; but the form is different, the elytra suddenly widening from 162 REV. H.S. GORHAM ON NEW COLEOPTERA. [Mar. 16, the shoulder, and the thorax having the base narrower with the hind angles right angles, so that the insect is not so uniformly round as in its allies. The antenne are formed much as in VS. vallatus, the second to eighth joints being short and bead-shaped, but longer than wide, the club strong but laxly jointed, the apical joint quad- rate and much (fully twice) wider than the ninth. The thorax is wider than long, narrowed to the front angles, but with its sides nearly straight in the basal two thirds ; its fattened margin has its internal edge deeply impressed in front, where the flat part is widest, and it appears raised at the base only, where the disk is widely suleate ; the disk is convex, minutely but distinctly covered with small points, but the puncturing is much obscured by coarse floccose pubescence. Only one specimen of this interesting species was obtained. PANOM@A. 1. Panoma@a CINGALENs!Is. (Plate XVII. fig. 2.) Rufo-testacea; capite et thorace basi piceis ; antennarum clava, articulo basali externe, scutello, sutura elytrisque maculis quinque sat magnis nigris ; antennis articulis decem. Long. 5 millim. Hab. Ceylon, Hadley (Lewis). Antenne ten-jointed, the basal joint is stout, a little curved, the second is scarcely longer than broad, and the third is apparently longer than usual, and is possibly really composed of the third and fourth joints together, but I can see no suture; the fourth to the seventh very short, club lax, the eighth and ninth joints rather trigonal. Head pitchy, smooth; eyes coarsely granulate (as in typical Panomea). Thorax as in P. pardalina, but anterior angles rather more prominent, scarcely punctured, but a little uneven at the sides, finely margined, except at the middle of the base. Elytra more cordate than in other species, and viewed sideways rising to a point so as to appear more gibbous than in its allies, finely but closely punctured, with five largish black spots—one humeral, two near the suture, one marginal (larger than the others), one subapical ; this last in one example connected with the marginal one ; the under- side and legs are deep ferruginous red. Five or six examples were obtained. ENDOCa@LUS, N. g. Mr. Lewis has met with a very curious small beetle in Ceylon, which apparently comes very near Panomea, which itself is synony- mous with Cyclotoma of Mulsant, and of which a short description will be sufficient to render its identification certain. The antenne, however, appear to me to be ten-jointed, and the two basal joints to be stout, the third to the seventh to be very short, the three last forming an elongate lax club. The tarsi are four-jointed, almost linear, very similar to those of Rhymbus. Hanhart imp NEW COLEOPTERA OF THE FAMILY ENDOMYCHIDE 1886. ] ON THE SO-CALLED PELVISTERNUM. 163 1. ENDOCG@LUS ORBICULARIS. Rotundatus, ferrugineus ; elytris convewis, fortiter parce punctatis, setulosis, marginibus latius eaxplanatis, apice subacuminato ; thoracis margine elevato deplanato, basi sulcis duobus puncti- Sormibus. Antennarum clava fusca. Long. 14 millim. Hab. Ceylon (Lewis). Orbicular, elytra subglobularly convex, with their lateral margin much expanded in the middle, but the widened rim vanishing in the apex, where they are conjointly deflexed and acuminate ; their disk is evenly and strongly punctured, the margins less distinctly ; the extreme limb of the expanded margin is itself finely reflexed. The head is exserted, with small prominent coarsely granulated eyes. The maxillary palpi have their apical joint subulate. The thorax is short, narrowed in front, with the margin raised, thickened and flattened as in Stenotarsus, the front angles being rounded in to form the emarginate opening for the head, than which it is much wider ; the base is narrower than the elytra at their base, and is furnished with two very deeply impressed punctiform sulci, which are about halfway between the centre and the hind angle, on each side. One specimen, taken at Dickoya. EXPLANATION OF PLATE XVII. Fig. 1. Cymones cowani, p. 158. 2. Panomea cingalensis, p. 162. . Cymones helopioides, p. 158. sharpi, p. 157. . Spathomeles? inflatus, p. 154. . Stictomela chrysomeloides, p. 156 . Epopterus lineoguttatus, p. 161. ephippiger, p. 160. eganus, p. 160. OMAR OP coh 2. On the so-called Pelyisternum of certain Vertebrates. By R. J. Anprrson, M.D., M.A., Professor of Natural History, Queen’s College, Galway. [Received March 1, 1886.] Prof. Paul Albrecht in 1883 described! an interpubic bone which he found present in Dasypus sewcinctus, Bradypus cuculliger, and Cholepus didactylus. He compares the symphysial cartilage found in many animals and this bone with the parts of the sternum, shoulder-girdle, and os hyoides, and gives several very instructive and clear figures of specimens in the museums at Berlin and KGnigs- berg. The figures of the Lacertilian pelves are copied from the papers of Profs. Huxley and Wiedersheim, and the scheme of homology he represents in a table at the end of his note. * Bull, d. l’Académie royale de Belgique, nos, 9-10. 164 DR. R. J. ANDERSON ON THE [Mar. 16, PELYIC GIRDLE, SHOULDER-GIRDLE, 1. Pubis. 1, Procoracoid. 2. Ischium. 2. Coracoid. 3. Ilium. 3. Scapula. 4, Subilium. 4, Subscapula. 5. Wanting. 5. Clavicle. 6. Wanting. 6. Interclavicle. 7. Pelvisternum. 7. Omosternum. (Ischio-pubic symphysial carti- Coraco-procoracoid symphysial lage. Osseous pelvisternum of cartilage. Edentates. ) 8. Hemi-pelvisternum. 8. Hemi-omosternum. 9. Ischio-pubic symphysis. 9. Symphysis coraco-procoracoid. 10. Prepelvisternum. 10, Preomosternum. Preomosterna of Anoura. 11. Hemi-pelvisterna. 11. Hemi-preomosterna. Epipelvic ossicles of Ohame- Substernal bones of mammals. leons. Marsupial bones of Monotremes and Marsupials. 12. Post-pelvisternum, 12. Post-omosternum, Os cloace of Lacertilians. The pelvis of Lacerta muralis is figured by Prof. Hoffmann in Bronn’s ‘ Thierreichs,’ and Brihl also gives figures of the Amphibian forms. In a specimen of Iguana tuberculata in this museum the pubis is a separate bone, and contains a preacetabular foramen as well as a well-marked supra- or prepubic notch. A copula (bone) teaches from the anterior part of the ischium to the pubis, wider behind than in front. The os cloacze fits into the ischial symphysis behind, and the ischial symphysis still shows the marks of union-with the tuberosities. The ilia articulate each with two transverse pro- cesses, and the traces of union with the ischium are obliterated. In the Australian Monitor gouldii which we have, a prepubic nodule fits in between the pubes in front ; all traces of union between the parts of the ossa innominata are obliterated. A small nodule is situated in front of the ischial symphysis, and a distinct os cloacee is present behind, and, as in the Iguana, fits in between the ischia. A prominent ischial spine behind is situated at the junction of the middle and outer third of the posterior border of that bone. In Lacerta viridis a prepubic nodule and a postischial are present. In the West-Australian Moloch horridus (marked 1845 in the catalogue) the postischial bone is quite evident, and a large copula runs forwards to the pelvis. In our Chameleon the three pelvic bones are short, and the os cloacee seems to be cartilaginous ; the ischio-pubic copula is reduced to a thread-like structure. The os cloace and prepubic bone are thin in our specimen of Ameiva, but they are very distinct. Prof. Owen, in his ‘Anatomy,’ says that in the Potoroo there is a triangular ossicle developed at an early period, which is wedged into the posterior interspace of the ischio-pubic symphysis; and in his paper in this Society’s ‘Transactions’ he figures the posterior epiphysial bone. In the skeleton of a Kangaroo in our museum the following measurements were made :— 1886.] SO-CALLED PELVISTERNUM. 165 millim, enatiynh nbn ft 0G ae as OPS as 140 Wrenhray dnc. eit eth ey ile on arigizistnalSints 20 Breadth opposite the acetabulum ............ 35 Length of pubis ...... ee Interpubic bone, antero-posterior diameter .... 15 i. », breadth of one side ........ 35 In Phacocherus the bone occupies the position of the triangular ligament in man, and is three-cornered and wedge-like. The following measurements were made :— millim Length of os innominatum ................ 250 Crestisee: AS f6) p Pt 120 Breadth of lium above acetabulum LR RWAE BOSS 32 i tebat acetabulum. soe 87 » below acetabulum.......... 34 Arch of Paws: Hee I sie HO Wen fo Interpubic bone, breadth .......00.05.. 00.0 24 a jt superior depth’ 22.) 0) Ate a 15 iz sy tinferior depth i) ey Ai g.s8 30 BS >, thickness at base ..7....... 20 In the skeleton of the Beaver the bone is not so distinct as in Phacocherus. The following are the measurements :— millim _Length of os innominatum ................ 160 Cresta. ty 2K eat, 5 AW RI Oe In SAREE EOP SO Breadth opposite acetabulum .............. 35 PEC OGL DUIS IN SL Su PSOE ee eh AD Plept eb pubic Hone, 5.260. 8eU Es eg Breadth-otoneshalfrogs:.) 20h stein ae. 25 I do not find the bone present in any other mammalian skeletons that I have examined. The bone occupies the position of the triangular ligament and the os cloacze of Lacertilians. Ligaments and fascize are so often the seat of ossifications, and bones in one set of animals are so often represented by ligaments in another set, that one is almost tempted to regard the bones above referred to as, in whole or in part, homologous with the triangular ligament of the urethra found in the higher animals. The interpubic bone in Bradypus is mentioned by Prof. Flower in his ‘ Osteology.’ 166 PROF. F. J. BELL ON BIPALIUM KEWENSE. __ [ Mar. 16, 3. Note on Bipalium kewense, and the Generic Characters of Land-Planarians. By Professor F. Jurrrey Bett, M.A., Sec. R.M.S: [Received March 16, 1886.] (Plate XVIII.) In the descriptions given by writers on Land-Planarians especial attention is always directed to the form of the head or, as more than one author has called it, the tail. This, no doubt, is partly due to the fact that in a number of the species the head is often seen to have a remarkable hammer-shaped or cheese-knife form, which has three times led to the institution of a genus for the reception of such species. In other cases, where the worm has been assigned to other genera, the head is described as obtusely rounded, or as not sharply distinguished from the body. Having lately received from Mr. Osbert Salvin, F.R.S., a specimen of a Land-Planarian (apparently Bipalium kewense, Moseley), found by him among broken fiower-pots in his garden in Sussex, of the origin of which nothing definite is known, I have been enabled to watch the creature exhibiting its activity. I had not long been study- ing it when I noted that the head varied considerably and almost constantly in form, so that I thought it well to at once enlist the skilful pencil of Mr. C. Berjeau to represent its various appearances. Figure A represents the worm, not indeed at its greatest length, but in a position which it is apt to assume when in full activity ; the head is carried a litile higher than the rest of the body, its edges are sharp, its contour convex, and it is well marked off from the rest of the body. Figure B, on the other hand, shows the animal in a state of torpid quiescence ; the head is now contracted, obtusely pointed, only separated by a shallow depression on either side from the sur- rounding region of the body. Fig. C shows an intermediate condition between A and B. Figs. D-G show various stages in the form of the head ’\—hammer-shaped, knob-like, tongue-shaped, or altogether irregular. The body may be not more than 2 inches long, when the creature looks like a leech or a slug, or it may extend itself to 6 inches and even more, when it has rather the appearance of a thread-worm. In fact, as one looks at it extended on a white dish, it calls to mind the Ameba more than any other animal known to the zoologist. I insist on the variations in the form of the body, and especially of the head, because all writers (even those who, like M. Humbert, Prof. Moseley, or, the latest of all, Dr. J. C. C. Loman, have had the opportunity of examining these forms alive or under natural condi- tions) direct, in their descriptions, especial attention to the form of the head ; indeed, land-planarians with cheese-cutter or hammer- shaped heads (ef. figs. A and D) have been by all naturalists ’ All the figures are of the natural size. 1886. ] PROF. F. J. BELL ON BIPALIUM KEWENSE. 167 assigned to the genus Bipalium’. The only writer who seems to have remarked the variability in the form of the head is M. Hum- bert, who figures* the head of Bipalium diana, as living and when it is greatly contracted ; the differences are, however, quite slight as compared with those in the figures now given (Plate XVIII.). More- over, M. Humbert continues to use the form of the head as a distinctive character, and seems to have only incompletely appreciated the moral of what he saw. Referring to the paper of Prof. Perceval Wright, M. Humbert says:—‘Il donne une figure .... qui représente Pextrémité antérieure semilunaire et a du evidemment étre faite daprés un individu conservé dans l’alcool, tandis que celle de la D. grayia a été dessinée d’aprés le vivant. C’est sans doute 4 ces deux maniéres d’observer, encore plus qu’A des particularités spécifiques qu’il faut attribuer les différences profondes que l’on remarque dans la forme des extrémités antérieures de ces deux espéces.”” But the differences shown in Prof. Wright’s woodcuts of the two species are not as “ profound” as those seen in the figures of the single living specimen here reproduced. So that, though M. Humbert recognized the difference between living heads and heads preserved in spirit, he does not seem to have recognized what is much more important—that the form of the head varies constantly during life. Ifa Planarian in a torpid condition (Pl. XVIII. fig. I) be then and there seized and put into spirit, it will be found, no doubt, to have an obtusely blunted head, hardly wider than the body*; on the other hand, some, at any rate, if killed while in full activity, will be found to have heads shaped like a cheese- cutter or some modification thereof. Hab. Mr. Salvin has lately received orchids from 8. America and S. Mexico, and from Burmah ; but he has also had specimens from Kew Gardens, whence the originals came to Mr. Moseley. In 1883 Dr. Giinther received some specimens from Welbeck Abbey*, where they had been known for three or four years pre- viously ; Mr. Thiselton Dyer tells me that there is no history of any communication between the gardens at that place and Kew, and adds “‘ we have probably therefore been stocked from a common source.” A specimen found in a greenhouse in Clapham Park was sent to Dr. W. M. Ord, and is now in the possession of Prof. Ray Lankester ; the early history of this specimen is unknown. In the hope of being able to extend our knowledge of this worm, I have written a note to the editor of the ‘ Gardener’s Chronicle’ °, which may result in some further information, and perhaps in the discovery of fresh examples * The French translator of the latest authoritative work on General Zoology by converting “ Kopftheil durch Lappen-Vorsatze halbmondformig” into “ Région céphalique en croissant par la présence de deux appendices lobés,” shows that he too regards the lateral parts of the head as being constant in form and position; nevertheless they are not so. * Mém. Soc. Genéve, xvi. p. 303, figs. 1, 1a. * Fig. H in Plate XVIII. shows the form of the head in the specimen under description, now that it is dead and preserved in spirit. * See his letter in the ‘Gardener’s Chronicle,’ xix, (1883) p. 415. ® Published on March 13th, 1886. 168 MR. F. E. BEDDARD ON A LARGE EARTHWORM. [ Mar. 16, and new localities’. I am inclined to think that such information will support Dr. Giinther’s supposition that the worm has become acclimatized in this country ; Mr. Dyer tells me that it is still to be found in the Kew hothouses, where it has now lived since at any rate the beginning of 1878. k Prof. Moseley was able to observe in Ceylon that Bipalium suspends itself by the tough slime which it secretes. My specimen had no opportunity of showing if it could so support itself; but I noticed that minute offending objects could be got rid of by being entangled in the slime which it secreted, and which, being gradually secreted from a point, say, one inch behind the head forwards, was as a continuous sheet of mucus thrown off from the anterior end. A small earthworm which was placed near it, but which was not attacked, had the same mucous sheet thrown over it, to its obvious embar- rassment. There can be-no doubt as to the sensitiveness of Bipalium to light. The specimen now under notice was sent by Mr. Salvin on February 7th, lived and was more or less active till February 26th; for this interval of time the town was either enveloped in fog, or surrounded by a darkness which needed not to be called back to our recollection. But on the 26th of February the sun shone, and though the room in which the Planarian had been placed was not illuminated by its rays, yet the exposure to diffuse light, which on other and earlier days had been harmless, was on this day fatal; the worm broke transversely into three pieces, and on being teuched fell into four. Had it been kept in darkness it is possible it might have lived longer. The temperature of the room varied from about 50° to 64° F. DESCRIPTION OF PLATE XVIII. Tllustrating the various forms assumed by Bipalium kewense. A. Extended and moving freely. B, ©. In various states of contraction. D-G. Some of the various forms taken by the head. H. Head and anterior end after contraction in spirit. I. The worm coiled and at rest. All the figures are of the natural size. 4, Note on the Structure of a large Species of Earthworm from New Caledonia. By Frank E: Bepparp, M.A., F.R.S.E., Prosector to the Society. [Received March 15, 1886.] (Plate XIX.) Among a number of Earthworms forwarded to me from New Caledonia, through the kindness of Mr. E. L. Layard, F.Z.S., H.B.M. Consul at Noumea, were six specimens of a large worm several of which measured some 28 inches in length. All these specimens are referable to the same species, which belongs to the genus Acantho- 1 Specimens have been found in the Zoological Society’s Gardens, which have, and in gardens at Liverpool which have not had direct relations with Kew. FP. 2.5. 1886... Pl. XViL Berjeau & Highley del et lith Mintern Bros . imp. BIPALIUM KEWENSE.. IN VARIOUS STAGES OF CONTRACTION. he aoe ey ah ‘ ee eh . > é a “4 : A: . . ’ 7 ta ‘ ¥ si eres ¥ : , t oe he ee Ae nt ve AL ee Pi BE te ‘ ie ite at of ‘ ha Sy a ry x - we 1886.] MR. F. E. BEDDARD ON A LARGE EARTHWORM. 169 drilus’. This genus is already known to inhabit New Caledonia ; M. Perrier bas des¢ribed two distinct species from that region. The species which forms the subject of the present communication may be identical with one or other of these. The descriptions given by M. Perrier of Acanthodrilus obtusus and A. angulatus are necessarily insufficient, owing to the poor condition and immaturity of the specimens at his disposal ; but certain facts, such as the position of the generative apertures and of the clitellum, could hardly be mistaken even in specimens greatly injured through bad preservation ; in these points the present species differs from both of those de- scribed by Perrier, as will be apparent from the following notes on its structure. External Characters.—I have sketched (Plate XIX. fig. 1) the anterior segments of the body from the dorsal aspect to indicate the main external features which are visible upon that surface. The buccal lobe divides the first segment *, as also in A. dissimilis and A, nove zelundie, two species recently described by myself *. Ofa fourth species of the genus, viz. 4. verticillatus, M. Perrier writes * :— ** La lobe céphalique n’entame pas le premier anneau et parait au contraire s’elargir asa base de maniére aressembler a la partiesupérieure d’un tréfle ; mais cette apparence tient peut-€tre a un état particulier de conservation.” J mention these facts because the genus Lumbricus has been split up into other genera mainly on this account. It does not appear to me advisable, while there = so many internal structural differences, to make use of so small an external character for classificatory purposes ; but in the case of the genus Acanthodrilus this mark of difference between species appears to be correlated with other differences of structure, inasmuch as M. Perrier hesitates to include A. verticillatus in the same genus with A. odbtusus; the male generative pores in the former species are upon the 17th and 18th segments and are not separated by an intercalated segment as in the Jatter and all the other species of the genus at present known. On either’side of the buccal lobe, and consequently between the first and second segments of the body, is a single pore; these may perhaps correspond to the single median dorsal pore which is the only orifice of the kind found in the Oligocheta limicole. The celitellum was fully developed in several specimens, and extended from the 13th to the 17th segments inclusive, with the exception of a portion of the 13th segment; the glandular tissue composing the clitellum was only visible on the posterior half of that segment ; the clitellum extends occasionally for a short distance on to the 18th segment. The anterior region of the clitellum down to the 15th segment completely encircles the body ; the 17th and 18th segments, on the contrary, have a very considerable median area upon which there is no glandular development ; the lateral margins of this ? Perrier, “Recherches pour servir alhistoire des Lombriciens terrestres,” Nouy. Arch. d. Muséum, t. viii. (1872) p. 85. * I have reckoned the first seta-bearing segment as the second segment of the body, in common with the majority of naturalists who have studied this group. * P.Z.S. 1885, p. 813. * Loe. cit. p. 93. Proc. Zoo. Soc.—1886, No. XII. 12 170 MR. F. E. BEDDARD ON A LARGE EARTHWORM. [ Mar. 16, area are bounded by the ventral pair of setz; this area, which is distinguished by its very pale colour, surrounds the male genital apertures, which are upon the 17th and 19th segments respectively (see fig. 2). In A. ungulatus the clitellum extends from 14-17 inclusive and the male genital apertures are upon the 18th and 20th segments ; in A. obfusus the clitellum is unknown, the male genital pores are upon the 19th and 21st segments. Dorsal pores are stated by Perrier to be present in his two species ; in my species they are present and commence apparently at the 13th or 14th segment ; in one specimen the first dorsal pore was visible between the 12th and 13th segments, in a second specimen this pore was a segment further back. I have figured these apertures as extending over the clitellum, since they were visible on these segments in immature examples without a clitellum; when the clitellum was present they were apparently absent or, rather, perhaps rendered invisible by the swollen glandular integument. In Acanthodrilus multiporus (see P. Z.8. 1885, pt. iv. p. 810) I observed dorsal pores commencing after the clitellum, the first pore marking the posterior boundary of that region of the integument. In Acanthodrilus dissimilis and A. nove zelandie they appear to be present though very inconspicuous; I only noted them after the clitellum. In the furrows separating segments 7-8 and 8-9 were a pair of distinct rounded apertures corresponding to the inferior pairs of sete ; these are the apertures of the copulatory pouches. The pair of setee on segment 8 were in most instances greatly modified, being much larger and more conspicuous than the other sete of the body ; their appearance is very like that of the genital sete on segments 17 and 19. In describing the structure of the genital organs I shall call attention to those setze which correspond to internal structures entirely novel in this genus. The ordinary setz of the body are distributed in pairs as in other species of the genus. The apertures of the nephridia are very conspicuous and correspoud in every case to the more dorsal pair of sete. The female generative pores are displayed in fig. 2; they are a pair of very minute pores situated on the 14th segment in front of and to the inside of the ventral pair of sete; their position is nearly similar to the corresponding pores of A. nove zelandie ; they are on the same segment as in that species, where, however, the pores are placed in front of the outermost of the two ventral sete. In Acanthodrilus capensis I find the female generative pores are upon the 14th segment and the ovaries in the 13th segment, and not, as erroneously stated in my paper on that species’, in the segment anterior to these; in the present species, however, the pores are placed in front of the innermost of the two ventral setz. Vascular System.—In fig. 7 of Plate XIX. isillustrated the main vascular trunks of the anterior region of the body. The dorsal vessel 1 Proc. Roy. Phys. Soc. 1885-6, p. 369. 1856.] MR. F. E. BEDDARD ON A LARGE EARTHWORM. 171 (d), which is a single tube, and not composed of two separate or incompletely fused halves as in A. multiporus* and other Earthworms, communicates with the ventral vessel by seven transverse hearts (/) situated in segments 8-14 inclusive—a pair to each segment. The first three pairs are of less calibre than the following four, and appear to arise simply from the dorsal vessel; the four posterior pairs of hearts communicate also with a small supra-intestinal vessel, which, as shown in the figure (sz), lies beneath the dorsal vessel but above the intestine ; in the anterior part of the body a pair of lateral vessels (/) supply the body-wall; in the 11th or 12th segment these vessels pass beneath the intestine and unite to form a single subintestinal vessel. This vessel appears to be continuous posteriorly with a vascular space within the walls of the alimentary canal. Each of the two anterior pairs of hearts supplies the spermatheca of its own segment; a strong branch arises from the vessel just before it unites with the ventral vessel, and a corresponding branch from the latter is also distributed to the spermatheca. Body-cavity.—The body-cavity, as in all other Earthworms, is divided into segments by mesenteries which extend from side to side of the body ; in the six anterior segments the mesenteries are more or less distinct, but there are in addition a number of muscular bands and tendinous-looking threads which bend the pharynx down to the body-wall, often passing through the mesenteries on their way; the gizzard and a portion of the anterior region of the cesophagus are only attached to the body-wall by a very few slight threads, mesenteries being absent in this region of the body. The mesentery which bounds the tenth segment behind and the succeeding four mesentries are specially thickened and muscular. Nephridia.—TYhere is a very considerable variation in the cha- racters of the nephridia in this genus, and I have already* referred to what has been written on the subject. In the present species the nephridia (fig. 6, 2) are very conspicucus, especially in the anterior region of the body as far back as the 19th segment or thereabouts ; in the posterior segments they are present but appear to differ slightly, principally in size, from the anteriorly placed nephridia. The external apertures are plainly visible in front of the dorsal pair of setz in all the seta-bearing segments of the body ; that is to say, the first segment of the body appears to be without nephridia and cnly this segment. The glandular portion of the nephridium forms a closely packed tuft of tubules which has much the appearance of the nepbridia in those species of Pericheta* in which these organs have been described ; this glandular tuft lies in the region of the ventral pair of setze and close to the mesentery which forms the anterior wall of its segment ; the nephridium communicates with the exterior by a long, widish, thin-walled duct. bord 1 See F. E. Beddard “On the paired Dorsal Vessel of certain Earthworms.” Proc. Roy. Phys. Soc. 1884-5, p. 424. 2 P. Z.S. 1885, p. 822. * E. g. Pericheta indica, Horst, Niederl. Arch. f. Zool. Bd. iv. (1879), pl. viii. fig. 3, x. 12* 172 MR. ¥F. E. BEDDARD ON A LARGE EARTHWORM. [Mar. 16, Generative System.—In the 12th segment are a pair of glands attached firmly to the mesentery which separates this segment from the one anterior to it; in two specimens these glands were paired, while in a third only the left-hand one of the two was present; in one specimen these glands have a racemose structure, and although a microscopic examination did not reveal any structure, I have little doubt that these glands are testes. Out of the seven examples at my disposal one specimen possessed a similar pair of glands in the 11th segment in addition to those found in the 12th segment ; in all the remaining specimens save one, which was small and immature, the 10th segment (that which follows the segment con- taining the posterior pair of spermathecz) has a pair of glandular- looking bodies which are very similar in general appearance to the structures which I have regarded as the testes; they are attached, however, to the posterior wall of their segment, which, as in other Earthworms, is not separated by a mesentery from the 9th segment; these two segments, which are thus fused, contain the gizzard. The fact that these glands are attached to the posterior and not to the anterior wall of their segment is perhaps against the view that they represent an anterior pair of testes; at the same time it happens that the segment in which they occur has no anterior wall, being fused with the preceding 9th segment; these glands were not present in the only specimen that had two pairs of testes. In Acanthodrilus capensis’ there are three pairs of testes situated in segments 10, 11, and 12; but out of a number of examples that I dissected only one had the three pairs developed. There is therefore nothing unusual in supposing that the present species, like 4. capensis, has three pairs of testes, although all the other species that are known appear to have only two pairs. On the other hand, the gland in segment 10 is very similar to a curious structure which exists in 4. capensis ina similar position, 7. e. attached to the posterior wall of the segment. In this species, however, the gizzard happens to be placed in front of the copulatory pouches, and not in the segment which contains them; so that the two pairs of pouches are separated from each other and from the following segments by fully developed mesenteries, which, as already stated, is not the case with the species that forms the subject of the present communication ; in this species the gizzard lies in the 9th and 10th segments. If, however, these structures correspond to those recorded by me in A. capensis, it is no explanation of their nature ; in neither case is their function at all evident. The vasa deferentia were not visible. Each of the four male genital apertures are furnished with a long sac containing a number of penial sete which open on to the exterior in common with the duct of along coiled prostate gland, which appears to be similar in structure to the prostates of A. obtusus*; on the other hand, the characters 1 Proc. Roy. Phys. Soe. loc. cit. p. 3875. I have written 11, 12, and 13 in error ; the oyaries,as I have been able to assure myself by a subsequent examin- ation, are in segment 13, and so presumably the testes are in the three segments anterior to that which contains the ovaries, viz. in segments 10, 11, 12. 2 Perrier, loc, cit. p. 88. 1886.] MR. F. E. BEDDARD ON A LARGE EARTHWORM. 173 of the penial setae agree with those of A. ungulatus as described by Perrier '. The ovaries and oviducts I have been unable to find. There are two pairs of spermathece situated in segments 8 and 9 ; each consists of a spherical thin-walled sac communicating with the exterior by a long stout-walled duct which is often curved (see figs. 5 and 6, cp); at the upper extremity of the duct, where it unites with the sac, it becomes somewhat bulged out on one side, though there is hardly so marked a diverticulum as is figured by Perrier in A. ungulatus”. A very characteristic and remarkable series of structures now remain to be described, before concluding the account of the genera- tive system. In describing the external characters attention was drawn to the modification of the lowermost pair of sete in segment 8; the ordinary sete, at any rate on one side of the bedy, have disappeared and are replaced by a conspicuous orifice through which protrude one or more stout long set, which appear on a naked-eye inspection to be very similar to those which project through the male genera- tive pores. Fig. 5 of Pl. XIX. represents the internal structures which correspond to these peculiarly modified setz; the latter are con- tained in a thin-walled transparent sac (s) precisely as are the genital sete ; on either side of this sac is a long somewhat sausage-shaped glandular body (g.4), which communicates by a slender duct with the orifice through which the sete project on to the exterior. The presence of these glands renders the whole structure more similar still to the male generative pore, except that the “ prostates” are paired. These structures were only present on the left side of the body in one specimen; in two others they were only developed on the right side; in two other specimens both immature, without a clitellum, these structures were entirely absent on both sides of the body; ina sixth specimen, which was also immature, with the elitetum undeveloped and with very minute spermathecee, the bundle of modified setze was plainly visible on both sides of the body, but without its accessory glands; in the seventh specimen, also imma- ture, there was no vestige whatever of these structures ; wherever they were absent the setze of the segment were perfectly nurmal. I am not aware that any structures of this kind have been described in any other species of the genus or in any other Earth- worm; they appear to be novel to the group. At the same time Perrier figures some structures in A. uxgulatus* which may be identical, though the figure and his description are insufficient ; the description (p. 92) is as follows :—‘ Les poches copulatrices sont situées aux anneaux huit et dix. Chacune est munie d’un lobe postérieur, assez petit, et n’a pas d’autre appendice. Dans le neuviéme anneau se voient plusieurs sacs glandulaires, séparés par une glande multifide”’ The details are evidently different from the structures that I have just described, but the similarity of position, between the two spermathecze, renders it possible that they are identical ; in 1 Los, cit. p. 90, pL ii. figs. 21, 22. * Loe. cit. pl. ii. fig. 20. 3 Loe, eit. pl. it fig. 18, x. 174 MR. F. E. BEDDARD ON A LARGE EARTHWORM. [Mar. 16, my spec‘es, however, these structures are in the same segment as that which contains the anterior spermatheca and are not in a segment intercalated between those which contain the anterior.and posterior pairs of spermathece respectively. One of the sete is displayed in the drawing (fig. 3), and the lower extremity, more highly magnified, in another drawing (fig. 4); the general aspect of these setee is very similar to that of the penial setee. The seta is curved slightly towards the extremity; its thickness diminishes gradually until near to the distal extremity, where it becomes again thicker and terminates in a swollen brush-like extremity, the exact shape of which can be gathered from an inspection of the figure. The distal extremity of the seta is ornamented with delicate transverse ridges projecting like the edges of scales and denticulated. In Luméricus Hering’ has described, and Vejdovsky * confirmed for other species, the modification of certain of the sete in the neighbourhood of the genital orifices ; those of the ventral pair in “the 10th, 15th, orone of the neighbouring segments, and furthermore in the region of the 26th segment and on the clitellum from segment 31 to segment 38 ”: these sete are more slender than, and double the length of, the ordinary sete of the body. In the work referred to Vejdovsky goes on to point out that the penial setee in Aeanthodrilus and other genera probably correspond to these and differ from the genital setze of Chetogaster &c., which are developed during the breeding-season in the neighbourhood of the ordinary locomotor set, and in addition to them ; the penial setee of Acanthodrilus replace the ordinary locomotor sete. Since in Lumbricus the modified setze developed in the generative segments are not confined to a single segment. or even to the segments bordering upon the male generative pores, it is perhaps not surprising to find that in the present species of Acanthodrilus there are additional sacs of penial setee besides those normally found in the 17th and 19th segments of the body. The modified sete of Lumbricus are also furnished with a gland which projects into the body-cavity; these are appar- ently the capsulogenous glands of D’Udekem and Lankester, which are the equivalents of the setigerous glands, being simply enlarged in order to assist in the generative function. In Acanthodrilus multi- porus I have figured a pair of glands * corresponding to the setz which are probably the homologues of these glands, and I imagine that in the species of which the present note treats the two large glands related to the modified setee of segment 8 are in all proba- bility to be referred to the same category and are not special structures. After the foregoing notes.on the structure of this Earthworm I may briefly refer to those points which seem to indicate that it is a distinct species differing from both the other two Acanthodrili which inhabit New Caledonia. With regard to external characters it appears to agree with A. ungulatus in the segments occupied 1 Zeitschr. f. wiss. Zool. Bd. viii. p. 418. ? System und Morphologie der Oligochxten (Prag, 1884), pp. 156-7. Ann. Se. Nat. 7° série, t. xix. pl. i. fig. 6 4. wo P. 2:9. 3886, Fl aie Mintern Bros. imp. ACANTHODRILUS LAYARDI1. 1886.] MR. F. E. BEDDARD ON A LARGE EARTHWORM. 175 by the clitellum, but to differ from both this and A. odtusus in the position of the male generative pores. The genital sete of the 17th and 19th segments are almost exactly like those of A. ungulatus, but the prostate glands, asin A. obtusus, are cylindrical coiled tubes and not multilobate glands as in A. ungulatus ; at the same time the prostate glands in several examples of my species are so closely coiled that they present an appearance which might easily be mistaken for that which has been stated by M. Perrier to be characteristic of A. ungulatus ; it is just possible that the condition of the specimen dissected by M. Perrier may be responsible for the lobed appearance of the prostate glands. Another difference between my species and A, ungulatus is in the spermathecee, which can hardly be said to have a diverticulum, and are in segments 8 and 9, not 8 and 10. The structures lying between the two spermathece of each side may, as I have already suggested, be identical with that described above, but evidently differ in detail. The most important difference between the species described here by myself and those of M. Perrier is undoubtedly in the position of the male generative pores ; in so many species—in fact in all except A. obtusus, A. verti- eillatus, and A. ungulatus—the male generative pores are upon the 17th and 19th segments’. EXPLANATION OF PLATE XIX. Fig. 1. Acanthodrilus layardi; anterior region of body, dorsal aspect. 2. Segments 13-20, from ventral side, to show position of female generative pores upon 14th, and the male generative pores upon 17th and 19th segments. The clitellum is indicated by shading. 3. Genital spicule from segment 8, magnified. 4. The lower extremity of the same, more highly magnified. 5, Spermathece and accessory genital glands: cp, spermathece ; v, ventral blood-vessels giving off branch to the spermatheca ; a corresponding branch is also given off from lateral heart; s, sac containing modified setae (figs. 5, 4); g.6, glandular bodies opening in common with seta sac; 7, glandular tufts of nephridium ; 2’, duct of nephridium. . Anterior region of body dissected : cp, spermathece ; 7, nephridia. . Principal vascular trunks of anterior region: d, dorsal vessel ; s7, supra- intestinal; v, ventral ; 7, lateral; , ‘ hearts.” bee Or) ' Referring to my paper already quoted upon the New-Zealand species of the genus, I find that the male generative pores are there stated to be upon the 16th and 18th segments. A reexamination of the specimens has convinced me that that statement is wrong, and that they are, as in the present species, upon the 17th and 19th segments, while the spermathecs are in the 8th and 9th seg- ments as indicated in the woodcut (P. Z. S. 1885, fig. 1, p. 815). Should the specimens to which the present note relates prove to belong to a distinct species from either of those described by Perrier, I propose to term the species Acanthodrilus layardt. 176 ANIMALS COMMENSAL OR PARASITIC [Apr. 6, April 6, 1886. Prof. W. H. Flower, LL.D., F.R.S., President, in the Chair. The Secretary read the following report on the additions to the Society’s Menagerie during the month of March 1886 :— _ The total number of registered additions to the Society’s Mena- gerie during the month of March was 121. Of these 6 were by birth, 58 by presentation, 11 by purchase, 1 by exchange and 45 were received on deposit. The total number of departures during the same period, by death and removals, was 127. The most noticeable additions during the month were :— 1. A second specimen of the Rough-billed Pelican of North America (Pelecanus trachyrhynchus)', purchased March 2nd. 2. An example of the White-tailed Ichneumon (Herpestes albi- cauda) from Lamoo, East Africa, presented by F. J. Jackson, Esq., F.Z.S., March 4th. The Secretary exhibited, on behalf of J. B. Martin, Esq., F.Z.S., a large tusk of the Indian Elephant (E/ephas indicus) belonging to the executors of the late Charles Reade, of which the length was stated to be 6 feet, and the weight over 100 pounds. The tusk was stated to have belonged to a ‘‘ rogue Elephant” which had ouly one tusk, and which had been killed at Goruckpore in 1836, when the late Charles Reade was magistrate there. Mr. Sclater exhibited the heads and horns of two species of Antelopes received by Lord Walsingham from Mr, F. J. Jackson, F.Z.8., having been obtained in the vicinity of Lamoo, East Africa. One of these belong to an adult specimen of Strepsiceros imberbis, Blyth; the two others to Damalis senegalensis, which, so far as Mr. Sclater knew, had not been previously obtained in this district. Strepsiceros imberbis had been already met with as far south as the Juba River on this coast *. Dr. H. Woodward exhibited specimens of animals commensal or parasitic in the shell of Meleagrina margaritifera, the Pearl- mussel, from the north coast of Australia, and read the following notes :— « The Pearl-shell fishery is now a recognized and important branch of the commerce of Western Australia, and also of Queensland and South Australia, which Colonies own the rights of the northern shores of that vast continent. “Mr. Thomas Harry Haynes has given me much interesting information regarding the pearl-shell fishery carried on by him and ? For uotice of previous specimen see P. Z. 8. 1883, p. 4638, plate xlyi. 2 See P. Z. 8S. 1884, p. 45. 1886.] IN MELEAGRINA MARGARITIFERA. 177 his partners on the N.W. coast of Australia, and has submitted many shells to me which had been attacked by lithodomous Mol- lusea, or by worms and the burrows of Cliona. “Some of these I have now the pleasure toexhibit. I have, more- over, to-day been permitted by Prof. Flower to examine a still more interesting specimen which he has just received from Henry Willett, Esq., F.G.S., of Arnold House, Brighton. “Tt is that of aspecimen of Pinnxotheres which has been entombed in a cyst of pearl by a living pearl-mussel, into the shell of which he had ventured to intrude. **Tt seems extraordinary and beyond belief that the Meleagrina should of all the Conchifera be the one to resent the commensalism of the Pea-crab, which has been known since the days of Cicero, Pliny, Oppian, and Aristotle to inhabit the shell of the Pinna and the Oyster, and has been recorded from Astarte, Pectunculus, and at least some half-dozen other bivalves, with whom it appears to live on the most friendly terms. “Tt is the females, however, which constantly reside within the shells of the Conchifera, whilst the males are said to avail them- selves of favourable opportunities to visit the females in their retirement. ‘** Whether or not in this case the unlucky male intruded himself upon Meleagrina at an unfavourable period, and finding no female Pinnotheres, penetrated so far beneath the mantle of the Pearl-mussel as to be unable to retreat, one thing is quite clear, namely that the Meleagrina entombed the intruder in a cyst of pearl from which the clever pearl-button maker alone liberated him. “ There is alargeseries of Pinnotheresin the Museum: the one from Australia is referred to P. orientalis, but as these are all females comparison is useless. These are from shells of Pinna, Donax, and Pectunculus. ‘There are others from Broken Bay. “ Prof. Dana, U.S. Expl. Expedition, 1852, part i. text, pp. 380— 381, and Atlas, pl. 24. fig. 3, describes a species under the name of P, obesa from Fiji Islands. The male, however, is said to be slightly broader than long, and the eyes (which in the adult female are quite hidden beneath the overreaching and protuberant carapace) can be seen in the upper view, and the front of the carapace is emarginated by the orbits. (Size 4? lines long, and 63 broad.) “Mr. Willett’s specimen is slightly longer than broad, and in size agrees very nearly with the male of P. pisum, which was formerly deseribed by Leach as P. latreillei.” The following papers were read :— 178 MR. F. E. BEDDARD ON THE [Apr. 6, 1. On some Points in the Anatomy of Chauna chavaiia. By Frank E. Bepparp, M.A., F.R.S.E., F.Z.S., Prosector to the Society. [Received March 15, 1886.] Prof. Garrod has contributed to the ‘ Proceedings’ of this Society some notes upon the anatomy, more particularly of the soft parts, of Chauna derbiana'. The recent death of one of the Society’s specimens of Chauna chavaria has enabled me to sapplement Prof. Garrod’s observations by some notes on the structure of the second species of Chauna. As might have been expected, there are no great differences between the ia) species; and with the exception of the colic caeca and the distribution of the tracheal muscles, all the statements made by Garrod apply equally well to the present species ; with regard to the visceral anatomy I am not able to institute a detailed compari- son between the two species, since certain of the facts which I shall describe in the present paper have not been referred to by Garrod in his account of Chauna derbiana. To these facts I have paid particular attention in order to render more complete our know- ledge of this interesting bird. dir-sacs, §e—On opening the body-cavity it was seen to be completely separated into a right and left half by a vertical septum attached above to the sternum and the ventral wall of the abdomen, and below to a horizontal fibrous septum which will be presently described. ‘This vertical septum anteriorly separates the two lobes of the liver and runs as far forward as the pericardium; _ it corresponds to the umbilical ligament, a structure which has not usually so great an extent in birds; more generally the umbilical ligament only extends as far back as the gizzard and terminates in a semicircular free posterior margin. In Chauna this vertical ligament bears a blood-vessel which joins the portal system anteriorly and posteriorly divides into two trunks, one of which passes further back than the other; this vessel is situated near the dorsal attach- ment of the septum. The horizontal septum is an extremely thick brown-coloured membrane which passes across the abdominal cavity from side to side, and completely covers the coils of the intestine, being attached laterally to the walls of the abdomen. This tough brown membrane corresponds to a structure described by Weldon (P. Z.S8. 1883, p. 640) in the Storks, and by myself (P. Z.S. 1885, p- 841) in the Cranes and other birds. This horizontal membrane when it reaches the gizzard splits into two layers which form a complete covering to that organ ; between it and the gizzard, on the inferior surface of the latter, are numerons air-spaces which were easily distended by inflating the air-sacs. The relations of the abdominal viscera are therefore, so far as the presence of this horizontal septum is concerned, indicative of an affinity with the Storks and Cranes, and more particularly with the * «Collected Papers,’ p. 318. 1886. ] ANATOMY OF CHAUNA CHAVARIA. 179 former group, since the lobes of the liver are not shut off by septa from the space which lies between the horizontal membrane and the ventral abdominal walls. In the Cranes, as in the Struthious birds, the lobes of the liver are enclosed in separate compartments distinct from that underlying the horizontal membrane (cf. P. Z.S. 1885, p. 836). There are other points in which Chauna approaches the Storks, In the paper already referred tc, Weldon has drawn attention to a peculiarity in the air-sacs of the Storks which appears to be characteristic of this group, and is at any rate not to be found in the Ducks. The prebronchial air-sacs (in the Storks and Pheeni- copterus) are divided by a complicated arrangement of transverse septa into smaller chambers. In Chauna chavaria this subdivision of the preebronchial air-sacs is very much more marked, and the subbronchial air-sacs, which in the Storks and many other birds are fused into a single cavity, are in the same way divided up into an immense number of extremely small chambers, so that the whole air-sac presents the appearance of a crowd of air-bubbles closely pressed together of various sizes. It was quite impossible on this account to distinguish the prebronchial from the postbranchial sacs, that is to say at the points where they come into contact. The prolongations of the subbronchial air-sacs into the axilla and into the space between the two pectoral muscles were similarly sub- divided by innumerable septa. There appeared to be nothing remarkable in the disposition of the abdominal air-sacs, and there were no indications of any subdivision of these charmbers; the anterior intermediate air-sac cominunicates with the bronchus by two apertures placed side by side and at some distance from each other near the anterior end of the. chamber; in the posterior intermediate sac, which was considerably the larger of the two, there was only a single pulmonary orifice. The abdominal air-sacs present the usual character—the right being considerably larger than the left. It appears to be the general rule that the thoracico-abdominal air- sacs are not divided up in the way that the cervical air-sacs are in Chauna and in the Storks; but I have met with occasional variations in the structure of their air-sacs in some few out of the numerous birds which I have had the opportunity of dissecting. In Steatornis I have already (supra, p. 151) called attention to the fact that the posterior intermediate air-sac was either completely separated into two distinct compartments or had indications of such a division ; in a specimen of Striv flammea there was a similar division of the posterior air-sac, at least on one side of the body. The third instance is Platalea leucorodia ; in a specimen of this bird, on both sides of the body there were three ‘intermediate ”’ air-sacs, the third being very small and interpolated between the anterior and posterior intermediate sacs. This may of course be an abnormality’; but the air-sacs of birds differ so little that any fact seems worth recording ; and the * A second specimen had the normal number of abdominal air-sacs. (o2) ON THE ANATOMY OF CHAUNA CHAVARIA. [Apr. 6, Will, I} i} 1) Mi LL Crea of Chauna chavaria. ee Or eee fas of i, 1886. | ON A BRACHIOPOD OF THE GENUS ATRETIA. 181 fact that the modification of the posterior air-sacs in Platalea was carried out on doth sides of the body perhaps shows it to be a characteristic of the bird. Alimentary Canal.—The ceca of Chauna chavaria appear to differ slightly from those of Chauna derbiana, the most noticeable difference being that they are not symmetrical in the former species ; the right cecum is slightly longer than the left, and is of a uniform conical shape, tapering slightly to the free extremity ; it measured 33 inches from the tip to the junction with the ilium ; the left cecum measured as nearly as possible 3 inches. The left czecum also differs in its shape, as may be seen by an inspection of the accompanying drawing (p. 180); its proximal half is about equal in diameter to that of the right caecum, but instead of tapering gradually it narrows abruptly into the distal half, which is of about the thickness of the little finger. In the /iver the right lobe is larger than the left lobe, and, as in the other species, there is a large gall-bladder the duct of which opens into the duodenum below the hepatic duct ; the pancreatic duct is the most anterior of the three. Trachea.—The extrinsic muscles of the syrinx are somewhat differently disposed from those of Chauna derbiana; as in that species, there are two pairs ; the most anterior spreads out in a fau-like manner upon a tough membrane which connects the coracoid and clavicle; this muscle is therefore attached exactly as is its homologue in Ch. derbiana. The posterior pair of muscles are, however, not attached to the costal process of the sternum as in Ch. derbiana, but terminate upon the aponeurosis of the lung just behind the exit of the pulmonary vein. The syrinx itself does not appear to me to be worth a special description or figure, as it agrees in every particular with that of Ch. derbiana. 2. On a Brachiopod of the Genus Afretia, named in MS. by the late Dr. T. Davidson. By Miss Acnrs Crane. (Communicated by Prof. W. H. Flower, LL.D., F.R.S.) [Received March 15, 1886. ] In July last the late Dr. Thomas Davidson, F.R.S., received from Mr. John Brazier, of Sydney, a gift of an interesting series of Brachiopoda dredged by him in the waters of Port Stephens and Port Jackson, New South Wales. When, in January 1886, it became my duty to select the remaining specimens from the Davidson collection necessary for the illustration of Parts 2 and 3 of Dr. Davidson’s forthcoming Monograph on Recent Brachiopoda, these Australian specimens were not found incorporated with his collection of living species. Possibly it was Dr. Davidson’s intention to describe them in aseparate paper. In February, when the collection of recent and fossil Brachiopoda (which, in accordance with Dr. Davidson’s 182 MISS A. CRANE ON A BRACHIOPOD [Apr. 6, desire, were presented to the nation) were removed to the Geological Department of the Natural History Branch of the British Museum at South Kensington, where he wished them to be deposited, Mr. Brazier’s series was found apart from the recent specimens with the fossil collection. Each species had been placed ina separate box with a number inside, and this number was found to correspond with Mr. Brazier’s list, which Dr. Davidson had copied into bis letter- book with his remarks appended. The executor instructed me temporarily to retain the series for examination. One very interesting new species of the remarkable genus Aéretia was discovered. This Dr. Davidson had named after his friend and correspondent Mr. John Brazier, of Sydney, who has dredged so extensively in Australian waters. The name 4Aéretia brazieri was attached in Dr. Davidson’s handwriting. The specimens are so excellent that there can be no possibility of generic error on my part, and I have therefore thought it my duty to publish a short description of Afretia brazier’, Dav., n. sp. MS., to secure priority for his last species, which should be figured in Part IT. of the Davidson Monograph of Recent Brachiopoda which I am now engaged in editing for the Transactions of the Linnean Society. Alretia, as its name implies, is an imperforate genus. It may be as well briefly to recapitulate the history of the type species, first published by Dr. Gwyn Jeffreys under the name Cryptopora gnomon in ‘Nature’ for Dec. 1869. In the ‘Ann. and Mag. Nat. Hist.’ 1876, Jeffreys gave the earliest description of the species, substituting the generic name Atretia for Cryplopora; Dr. Davidson gave the first figures in his Supplement to the “ Recent and Tertiary British Brachiopoda” (Pal. Soc. 1874), and again illustrated the species in one of the two plates he contributed to Dr. Jeffreys’s paper on “ The Mol- lusca (Brachiopoda) of the ‘ Lightning’ and ‘Porcupine’ Expeditions,” published in the Proc. Zool. Suc., April 1878. Atretia gnomon was dredged off the west coast of Ireland in from 1380-1443 fws. ; during the ‘Valorous’ expedition, 1100-1750 fms., in Davis Straits. It was found by Dr. Friele (during the Norwegian Arctic expedition) about 30 miles W. of Tromsé, in 650 fms., ‘‘on the slope of the banks cold area.”’? It was dredged off Marocco and the Canaries at depths of 50-65 fms., by the‘ Talisman’ and French expeditions. In all more than fifty examples of the European representative of this well-marked Rhynchonelloid have been obtained by Jeffreys, Friele, and the Marquis de Folin. M. Eugéne Deslongchamps, in his ‘ Etudes Critiques sur des Brachiopodes nouveaux ou peu connus,’ p. 242 (Caen, 1884), expresses an opinion that déretia gnomon, Jeffr., is probably only a very young stage of R. psittacea, Chemn. But the recent discovery by Mr. Brazier of eleven good specimens of the genus Atrefia in the Southern Pacific Ocean, off the coast of New South Wales, tends to invalidate that assumption, the only Rhynchonelle in the Australian and Novo-Zelandian region being the deeply ribbed or furrowed RA. nigricans and its variety, 2. pyxidata, Boog- Watson. To these well-characterized forms Atretia braziert, smooth, flat, 1886. | OF THE GENUS ATRETIA. 183 and compressed, bears no resemblance whatever, and exhibits at all ages definite generic characters *. ATRETIA BRAZIERI, Sp. nov. Description.—This pretty little Brachiopod presents all the well- marked characteristics of the genus, two short curved slender processes, denticulated at their extremities, descend from the small narrow hinge-plate of the smaller dorsal valve, and an elevated wedge- shaped projection rises abruptly from the central mesial septum of the same valve. The presence of this septum is indicated by a dark line visible from the exterior of the shell. The shell is small, generally longer than wide, triangular in shape, especially in the younger specimens. Dorsal valve rounder and not so large as the ventral one, slightly flexucus towards the centre at the margins of the valves. The ventral valve, owing to the prolongation of the beak area, is longer and more triangular than the dorsal one raised towards the beak, which is slightly produced and incurved, with a triangular foramen commencing beneath its pointed extremity. Two elevated ridges extend from the shoulder of the shell nearly to the margins of the valves, and there seems to be a slight elevation corresponding with the well-marked exterior depression and sur- rounded by muscular scars (?) in the exteriors of the ventral valves of two specimens I have examined under magnifying-powers. The shell is shallow towards the margins, but rounded and deeper near the beak. Shell-substance imperforate ; surface smooth, glossy, and gleaming, marked with fine concentric lines of growth ; semitrans- parent. Horn-coloured or light grey. Length 27 lines; width 14 line; depth about 1 line. Another specimen measured 2 lines in length by 2} in width; this was more flattened and depressed, and the external mesial sinus in the ventral valve was less marked. Other specimens were about | line in length. Station and Depth.—Eleven specimens and odd valves were dredged in twenty-five fathoms in sandy mud off Cabbage-Tree Island, Port Stephens, N.S.W., by Mr. John Brazier, who sent five specimens to Dr. Davidson, with the remark that they differed from all other known Brachiopoda from Australian waters. Obs.—Dr. Davidson commemorated Mr. Brazier’s discovery by naming the species after him, and I have deemed it my duty to my old and valued friend to describe the species under the name he desired to give it, as well as I am able. In so doing I wish to call the attention of qualified conchologists thereto, and to place on record the wide geographical distribution of the genus Afretia, which we now know to range in from 25-1750 fathoms, from nearly 70° N. ? Norr.—I communicated the discovery of the Australian A/retia to the Nor- Wegian naturalist, Herr Herman Friele, whu replied, April 19th, that my description of the skeleton of A. brazieri is quite typical of the genus Afretia, which he cannot consider to be the young of Rhynchonella. He adds the im- portant fact that he obtained some fifty specimens of the Atretia gnomon, Jetffr., during the Norwegian North-Atlantic Expedition, but no Rhynchonella occurred on the same station or in corresponding depths.—Agnes Crane, April 26th. 184 MR. J. G. GOODCHILD ON THE [Apr. 6, lat., in the Arctic Ocean to the Canaries in the South Atlantic, and as far as lat. 32° south of the Equator in the Southern Pacific Ocean. The specimens will eventually be placed in the Davidson Collection in the British Museum. P.S.—Since my paper on Atretia brazieri was writtten, I have submitted with my friend Mr. J. E. Haselwood, F. R. Mier. Soc., all the specimens of Afrefia to microscopic examination. Under a ten-inch power the beak-area deltidial plates present some imma- ture features similar to those figured by Morse in his ‘ Embryology of Terebratulina. The scaly structure of the shell is very apparent ; there are no perforations. We observed two long slender narrow muscular sears, with a diamond-shaped central one in the interior of a ventral valve. The marginal borders of the largest specimen seemed raised or swollen. The most puzzling appearance occurs on some brown patches on the shell, consisting of circular and elongated sac-~ like aggregations. If these bodies are a feature of the shell-structure, it seems strange they should be visible in portions of the surface only’. 1 hope further to investigate the matter. 3. Observations on the Disposition of the Cubital Coverts in Birds. By J. G. Goopncuitp, F.Z.S., F.G.S., H.M. Geological Survey. [Received March 16, 1886.] The prominent position occupied by the cubital coverts in most living birds renders their correct delineation a point of so much importance in any figure intended for zoological purposes that it is perhaps hardly necessary to offer any apology for submitting a few observations upon that subject for the consideration of the Fellows of this Society. Both ornithologists and zoological artists have, of course, long been aware of the existence of considerable diversity both in the relative proportions and in the mode of arrangement of these feathers in various groups of birds; but it seems never to have occurred to any one that these variations are of such a nature as to admit of their being reduced to any system of classification. This oversight may be due to the fact that the specimens made use of for scientific purposes have necessarily been either spirit-specimens or else skins flat or mounted. In the case of the skins especially, such specimens cannot, as a rule, be at all depended upon as repre- senting the natural order of the feathers in a living state; and consequently ornithologists have been led to believe that the subject under notice was not worth any serious attention. But a careful 1 Norz.—More prolonged examination by daylight with different powersp showed these appearances to result from the partial overlapping of the cycloidal scales of the shell-structure. The presence of parallel rows of spicular pro- jections was clearly revealed in the interior of the valves; these occur at regular distances from each other, running-from the beak towards the margins of the valves.—Aeners Crane, April 26th. 1886. ] CUBITAL COVERTS OF BIRDS. 185 comparison of the features presented by a large series of living birds, in good health, or of freshly-killed wild birds, leads to a different conclusion. These show that a particular mode of arrangement, or a particular order of overlap, of the median cubital coverts is practically constant for all the individuals of the same species. More extended observations show that the same general mode of disposition is as a rule characteristic of all the species of a genus, and may even be found throughout all the members of groups larger than that. A reference to the wing of the Golden Plover, a central type, and one that in itself represents all the leading modifications (see fig. 1, p. 186), may help to make the nomenclature herein used more intelligible. [In drawing up this scheme I have availed myself of several suggestions made to me by Prof. Flower, and by my colleague Mr. E. T. Newton, after the paper was read before the Society.] The terms used refer mainly to the relations of various parts of the wing to each other and to the body axis, when the wing is extended and is viewed from the dorsal or upper surface. The wing-surface is primarily divided into the manual (primary) region and the cubital (secondary) region, this last embracing all the feathers that originate from any part of the forearm or cubitus. Of the manual region I have nothing that need now be discussed. In the cubital region the Remiges, and the Greater Coverts that come on next above them, are uniform in disposition in all Carinate birds. In these feathers the overlap is uniformly distal ; that is to say, the several feathers are disposed in such a manner that the outer free edges of those nearer the vertebral axis overlap the inner edges of those originating nearer the distal extremity of the wing. The same observation applies also (but with some minor modifications of detail that will not now be taken into consideration) to the Lesser Coverts, or those feathers that mainly originate in the Patagium, and that extend along the anterior border of the wing from the humeral fold to the carpal joint. The remaining feathers, which are generally comprehended under the term Median Coverts, vary considerably in both their direction of imbrication and in the number of rows that run parallel to the greater coverts in each case. The present paper is devoted to a consideration of the nature and the extent of the variation referred to, without regard to morphological details of any other kind soever. Many of the facts have either not been noticed, or else, if they have been noticed, their significance appears to have been missed. For convenience of description the tract occupied by the Median Coverts may be divided into three areas by lines parallel to the main direction of the cubital quills. The area nearest the vertebral axis will be referred to as the Proximal area, the next the Middle area, and the remaining third, up to the distal border next the manual region, the Distal area. The rows of feathers composing the median eoverts range, in a general way, parallel with the greater coverts. The number of rows varies from one to six, or even more, in different forms of birds; and the row nearest the greater coverts is the one most subject to variation in the disposition of the feathers composing it. Proc. Zooxu. Soc.—1886, No. XIII. 13 186 MR. Jp G. GOODCHILD ON THE (Apr. 6, In dealing with the various modifications, I propose to take the birds as nearly as possible in the order adopted by Dr. Sclater in the Eighth Edition of the ‘ List of Vertebrated Animals now or lately living in the Gardens of the Zoological Society of London.’ Fig. 1. Illustrations of the terms used in the following description, as shown by the feathers of the Cubital Region in the Golden Plover. 1 to 1’. Posterior Border. 2 to 2’. Anterior Border. 2' to 1’. Proximal End. 2 to 1. Distal Edge of the Cubital Region (shown by the thicker line). A. Cubital Remiges. B. Greater Wing-coverts. C. Supplementary row of Median Coverts, or Upper Wing-coverts. D. Posterior row of Median Wing-coverts. HE. Second row. F. Third row. The Posterior row of Median Coverts from D, near the Carpal joint, shows Proximal Overlap as far as the point marked with a small cross. Distal Overlap is shown by the mode of imbrication of the Greater Wing-coverts. The Passerine style of imbrication represents one extreme of the range of modification observable, and is well exemplified by the wing of Zurdus merula (fig. 2). In this the median ecoverts consist of a single uninterrupted row of feathers, whose free edges are regularly directed backwards along a curve extending from near the carpal joint towards a point near the elbow. The same figure shows also one of the simplest arrangements of the Lesser Cubital Coverts. Such an arrangement as obtains in the Blackbird may be traced, with modifications of only minor importance, through some thousands of 1886.] CUBITAL COVERTS OF BIRDS. 187 species of Passerine birds, and will probably, on further examination, be found to characterize the whole of the birds that are correctly referred to that Order. In the Corvidze an approach towards a somewhat different mode of arrangement is made (fig. 3): another minor modification is seen in the Alaudidee (fig. 3a). The Swallows (fig. 5a, p. 188) all appear to follow the normal passerine type. That of the Swifts and the Cotingas appears to me to be essentially different. There is some doubt also in regard to the Bower-birds and the Birds of Paradise in this respect. Following Dr. Sclater’s arrangement, the Swifts and the Humming- Turdus merula. Corvus. Alauda arvensis. birds fall next to be deseribed. Living Humming-birds can very rarely be examined closely ; I have therefore been compelled to rely entirely upon the examination of museum specimens. After exa- mining the whole of the Gould Collection, and checking the results by comparing them with those made ona large series of other specimens, I am convinced that one general type of wing-pattern characterizes the whole of these birds; it is of a very simple character, and is represented in figure 4, p.188. By this it will be seen that the proxi- mal lapping row of median coverts found throughout all the Passeres is absent entirely in this. The Humming-birds might, indeed, be described as possessing no median coverts at all, the place of these being taken up by feathers having the same mode of imbrication as the Lesser Coverts. All the feathers of each series overlap outwards and backwards from the vertebral axis towards the distal end of the wing in these birds. Observations on the order of overlap in the wing of freshly-killed specimens of Cypselus apus, afterwards extended by an examination of the whole series of Swifts in the National Collection, showed that in these, as in the Humming-birds, no one series of feathers overlaps backwards. in fact the wing-pattern in the genera Cypselus, Acanthylis, Chetura, and Collocalia seems to me to differ in no essential respect from that found throughout the Trochilide. So far as the disposition of the wing-coverts is concerned, the Swifts and Humming-birds agree amongst themselves, and differ from all of the Passeriform birds, with the possible exception of the Birds of Paradise. Fig. 5, p. 188, taken from a freshiy-killed specimen of Cypselus apus, will serve to make this point clear. A wing of Hirundo rustica is figured alongside for comparison (fig. 5 a). Ia 188 MR. J. G. GOODCHILD ON THE [Apr. 6, Following the normal Macrochires come the Caprimulgide. Of these, in the living state, I have examined only Caprimulgus europeus and Podargus cuvieri. The disposition of the cubital coverts in these is certainly not at all like that seen in the Swifts ; but it closely follows the arrangement seen in the Picarian birds. In these at least two series of the feathers next above the Greater Coverts show proximal overlap. An examination of the specimens Fig. 5 a. Hirundo. Cypselus. Trochilus. ot Podargus, Batrachostomus, Agotheles, and Caprimulgus in the National Collection, as well as of specimens of the same family else- where, confirms this view. The soft and downy nature of the feathers prevents satisfactory observation upon any feathers above the two lower rows of median coverts; but I have satisfied myself in regard to the point in question. While Caprimulgus and its allies seem to agree in this particular with Podargus, Steatornis (so far as one can judge by the unsatisfactory data furnished by skins) presents yet another type, which seems to follow that of the true Cuckoos rather than that of Podargus or its allies. In all the remaining Fig. 6. Fig. 6 a. Fig. 6. ERR (WOON AK CLAS . / CE t= NWG , Ss My Chasmorhynchus. Dacelo. Tthamphastos. Picarian families enumerated in the List (except Cuculide, Muso- phagide, and Indicatoride), at least the two rows of feathers next 1886. ] CUBITAL COVERTS OF BIRDS. 189 above the greater coverts, and often more, show uniform and uninter- rupted proximal overlap. This arrangement can be very conveniently studied in the Toucans (fig. 64), which are nearly always well represented in the Parrot House in the Society’s Gardens. The Cuckoos are associated with the Picarian birds in the List; but as their wing-pattern differs in some essential respects from that of the typical forms, they will be referred to in connection with another series. The transition from the Picarian type to the Psittacine is gradual ; indeed some of the smaller Parrots, especially Melopsittacus, might, so far as the wing-pattern is concerned, well stand within the confines of the Picarian group. The chief difference in the case of Melo- psittacus lies in the further increase in the number of rows of back- ward-lapping feathers on the eubital area. Fig. 7 shows this form of wing, which can be easily compared with the living form in the case of so common a cage-bird. In the type of wing-pattern prevailing throughout all, or nearly all, the rest of the Psittacidz, an additional modification may be observed. The row of feathers coming on next above the Greater Coverts, indicated by the letter C in the following diagrams, is seen to consist of a series numbering generally five or six, which are confined tothe distal area of the cubital region, and form a distinct and separate series from the feathers that extend across the median area. They correspond in relative position to the Upper Wing-coverts (tectrices superiores) in the manual region of the wing; and it might be convenient for the present to refer to those extending over the distal area of the cubital region under the same term, as is done in the specimens Ulustrative of the structure of birds’ wings that Prof. Flower has arranged at the Natural-History Museum. The feathers referred Fig. 8a. Fig. 7. Psitiacus. Melopsittacus. Calopsitta. to often form a conspicuous feature on the wing of the living bird, as they are frequently arranged in such a manner that the shafts of three or more of the feathers are in a line. The proximal edges of these feathers are generally as firm as those on the opposite side, and, as a consequence, the whole series slides between the feathers next them on the proximal side in much the same way as the 190 MR. J. G. GOODCHILD ON THE [Apr. 6, blade of a lancet closes into its sheath. The feature referred to can be better understood by reference to C, figure 8, taken from a living specimen of Calopsitta nove-hollandie, which represents the style prevailing throughout probably the whole of the Psittaci. Essentially the same pattern as is found in the Psittaci prevails also throughout the whole of the Striges, and also throughout the whole of the Accipitres, with the exception of Pernis, Pandion, Gypogeranus, and the Cathartidee. These exceptional forms will be referred to again in their proper places. Fig. 9, representing the wing Falco. Phalacrocorax. of a Merlin, well illustrates the whole of the normal Accipitrine forms. Mr. Wolf’s beautiful figures of the Birds of Prey all afford excellent illustrations of the same point, while, from a part,of the world where experience has led us to expect minute accuracy of detail, we have the Japanese figure in metal of a species of Spizaetus, now amongst the choicest. treasures at South Kensington Museum, which affords a correct illustration of the Accipitrine style of cubital coverts. Of the Pelicans, in the present connection, nothing satisfactory can be made out, on account of the lax and drooping condition of their feathers, even in health. But Phalacrocorar (fig. 9a) gives us a style hardly distinguishable in any noticeable respect from that of the Accipitrines. On the other hand, Fregata, Sula, Plotus, and some other forms associated with them are widely removed, ptero- graphically, from the Cormorants. All the Herons and their immediate allies, Nycticorax (fig. 10), Botaurus, and, I believe, also Cancroma, closely follow the Accipitrine mode of imbrication. The principal difference lies in the reduced prominence of the supplementary row of lancet-like feathers (upper wing-coverts) so characteristic of the Birds of Prey and the Parrots. Healthy Night-Herons in immature plumage exhibit the Ardeine style of median cubital coverts remarkably well. The Ciconiide, in regard to the point under notice, will fall to be described in another part of this paper. 1886. | CUBITAL COVERTS OF BIRDS. 191 The remarks made in connection with the Pelicans apply also to the Odontoglossz. Passing over the Palamedez for the present, the last group whose style of cubital coverts brings them under notice here is the Anseres. Here, again, we have a group with nearly uniform pterographic Nyctieorax. Querquedula. eharacters ; these, as will be seen by reference to figure 11, repre- senting Querquedula crecea, so closely follow the style seen in the Accipitres and the others mentioned as possessing the accessory row of median coverts, or upper wing-coverts (C), that it is difficult to point to any one charaeter that would serve to distinguish them. It will be notieed that the birds characterized by possessing more than two rows of median cubital coverts with proximal overlap, together with a single supplementary row of upper wing-coverts also with proximal overlap, are further characterized by the Desmo- gnathous palate, are Homalogonate, and possess in addition several other deep-seated points of structure is common. Near to the Accipitrine birds, and perhaps leading away from them somewhere near the Polyborine birds, a kind of transition may be traced in the direction of the Gallinze. In the case of Meleagris (fig. 12) proximal overlap characterizes nearly all the median cubital coverts, as in the Accipitrines, and in this respect these birds stand 192 MR. J. G. GOODCHILD ON THE [Apr. 6, alone amongst the Gallinze ; but neither in Meleagris nor in any of the Alectoropods do any traces of the upper wing-coverts exist. In some respects the Peristeropod Gallinee, represented by Yalegalla (fig. 13 a) and by Craz (fig. 13), stand nearest of the Gallinze to the Accipitres; while Numida is hardly more removed. . Fig. 13. Fig. 13 a. CEA ve <= COMER EES GAUSS SERRE Sea TER Craxz, Talegalla. In the Peristeropods we find the commencement of a modification that is carried to a much greater length in other Galline birds, as well as in a large number of forms that have yet to be noticed. This consists in the increased prominence of distal overlap in the proximal. third of the cubital area. In Craw (fig. 13), for instance, it will be noticed that the distal overlap, whose commencement is indicated by the small cross, extends into the middle area in the case of the lowest tow. The distal overlap at C is another noteworthy feature, as it has not yet been observed in any of the Gallinz except the Peri- steropods. ] Taking the evidence afforded by the mode of imbrication of the wing-coverts alone, it is near to the Peristeropods, and not near to ; Fig. 14. Columba the Pigeons, that Goura should be placed. The pattern is shown in fig. 14, which should be compared with Craz on the one hand and 1886.] CUBITAL COVERTS OF BIRDS. 193 with any conspicuously-marked Pigeon of the normal type (Columba guinea, for example, fig. 14 a) on the other. The difference, to me, appears both striking and significant. Perhaps I. may be allowed to remark that the characteristic differences between Goura and the normal Pigeons are represented in the very useful series of coloured illustrations now. posted up outside the Western Aviary in the Society’s Gardens. In addition to the difference already noted between the true Pigeons and Goura, the following points of agreement and of difference between the two groups may be considered :— In the normal Pigeons an oil-gland is present; but is absent in Goura. In the normal Pigeons the tail-feathers are 12 in number ; while there are 16 in Goura. In the normal Pigeons the pterylosis is columbine ; and is galline in Goura. In the normal Pigeons ceca are present; but are absent in Goura. In the normal Pigeons a gall-bladder is present: no gall-bladder in Goura. - In the normal Pigeons incubation lasts 16 days; but extends to 28 days in Goura. _ In addition to these peculiarities reference may be made to the bird’s pheasant-like habits, to certain peculiarities of the urosacral and of the caudal vertebree, to the number of the cervical vertebre, to the absence of pterygoid processes, and to other features referred to by Prof. Huxley (P.Z.S. 1868, p. 302) and by Prof. Parker (Tf. Z. S. v. p. 151, 1863). Dr. Sclater (Ibis, 1880, p. 407) refers to certain peculiarities of the tarsus, in addition to the differences just noted, as evidence in favour of separating Goura from the Pigeons. The main differences that distinguish the wing of the Peristeropod Gallinze from that of the Birds of Prey have already been pointed out. It remains to add that the prominence of distal overlap introduced by Zalegalla, Crax and its allies, becomes more accentuated in Numida, and thence, through the Tetraonide (fig. 15, p. 194), reaches its greatest development amongst the Gallinz in the typical Pheasants. A progressive increase of distal imbrication can be traced, in the first stages, only in the first, or posterior, row of median coverts, then in the second, and the third, and so on, until in Polyplectron all the more conspicuous feathers in the closed wing of the living bird seem to lap from the proximal towards the distal side of the wing. Excellent examples of the features referred to may be easily observed in the Society’s Pheasant Aviary, where Lophophorus impeyanus, Huplocamus swinhoti, Phasianus reevesi, and Polyplectron chinquis well display the feature referred to. A reference to the annexed figure of Luplocamus swinhoii (fig. 16, p. 194) will serve to make the general disposition clear. Pavo follows a slightly different pattern; and it is a point worth 194 MR. J, G. GOODCHILD ON THE [Apr. 6, notice that there seems a constant difference of small amount between the individuals of P. eristatus and P. nigripennis now living in the collection. In P. nigripennis all the feathers of the posterior row of median coverts appear to lap distally. ‘The Common Peacock is Fig. 16. Euplocamus. well represented in the particular feature under notice by one of the fine pieces of Japanese metal-work at South Kensington already re- ferred to under the head of Accipitres. In the pterographie characters of both the Hemipodii and the Crypturi, I have hitherto failed to discover any marked charac- teristic connected with the point under consideration that would serve to distinguish these birds from the Gallinze. In the case of the Tinamous, especially, the structural characteristics of the palate had led me to expect a wing-pattern of a much lower type. With the exception of Goura, already noticed, the pterographic characters of the Columbe are remarkably uniform throughout. These characters are well displayed in the case of the Domestic Pigeon (fig. 17). Here it will be noticed that the proportion of feathers showing distal overlap, at the proximal end of the median coverts, remains much the same as in the Galline ; but that in place of the well-marked, uniform, and uninterrupted proximal overlap of 1886. ] CUBITAL COVERTS OF BIRDS. 195 the posterior, 2nd, and 3rd rows of median coverts in the distal area, which is nearly always seen in the Galline, the corresponding features of the Pigeon show a different and much more complex arrangement. In all the birds previously passed under notice (except the Birds of Paradise amongst the Passeres, and the Macro- chires) the feathers of both the middle and the distal area of the median coverts maintain a proximal imbrication from near the carpus backwards, various distances according to the zoological position of the bird under notice. In all the remaining birds, inclusive of the Columbe, the distal area of the median coverts is composed of feathers arranged in the opposite direction. It is somewhat difficult to reduce the facts to anything like an intelligible description ; but a study of the figures may help to make the mode of arrangement clear. It will be seen by this that several feathers on the distal area of each row overlap from behind forwards, or from the proximal towards the distal margin of the wing. The feature referred to can be easily studied in the case of Domestic Pigeons ; although the general Columbine pattern can, perhaps, best be studied in the case of such conspicuously-marked exotic Pigeons as Columba guinea, Peristera geoffroii, Leucosarcia picata, and others commonly living in the Western Aviary. : Pterocles arenarius, now (1885) living in the Western Aviary, shows an arrangement of the wing-feathers somewhat like that of the Pigeons, especially so far as the proximal and the distal areas of Péerocles. the cubital region are concerned. But the distal imbrication of all the feathers next the manual region is, in the Pterocletes, carried to excess. In this respect the Pterocletes stand as far removed from the Pigeons as these are from the Gallinee. Inthe stuffed specimens of Pterocles alchata in the National Collection this feature is remarkably well displayed (see fig. 18). Another point to be noticed in these birds is that the posterior row of median coverts show distal overlap throughout their entire length—an arrangement of 196 MR. J. G. GOODCHILD ON THE + [Apr. 6; these feathers that is characteristic of a large number of the birds remaining to be described. Still following the plan of tracing out the various modifications of wing-pattern without reference to any other characteristics, however important, the place of the Coccyges should be somewhere near the confines of the Columbe. Carpococcyx. Cuculus. Coecystes. In passing in review a number of species belonging to the Coceyges, they seem to be naturally divisible into the Cuckoos proper, well represented by Cuculus canorus (fig. 19), and the Centropodine, represented by Carpococcyx radiatus (fig. 20). The Cuckoos proper somewhat resemble the Pigeons, and where they differ from the Pigeons they seem to approach the Picarian birds. The Ground Cuckoos seem to make some approach to the Peristeropods; in other respects they remind one of the Musophagide. Judging from stuffed specimens alone, the wing of Opisthocomus closely resembles that of the Cuckoos. In the living Rustards, so far as I can judge, there seems again to be another variation on the general pattern of the Columbe ; but I have hitherto failed to obtain a satisfactory sketch of the wing-pattern in this bird. Ofthe remaining families of the Order Alectorides given in the List, I have also, so far, failed to obtain any good evidence, except in the case of the Gruidee, which will be referred to in more detail presently. It is especially desirable to obtain good observations upon the point specially under notice in the case of the Cariamas ; but the lax texture of their wing-feathers renders any such observation a matter of considerable difficulty. So far as I can judge at present, the style of coverts in the Cariamas agrees with that of the Bustards, and differs frem that of Serpentarius. The specimens of Chauna chavaria living at the Gardens present a style of imbrication that seems to approach the Columbine type very closely. The disposition shown in fig. 21 is practically the same as Wolf has drawn in Ch. nigricollis (=derbiana), P. Z.S. 1864, pl. xi. Whether the feathers of the distal tract of the cubital region follow exactly the same disposition as do those of the Pigeons 1886. ] CUBITAL COVERTS OF BIRDS. 197 I am at present unable to state definitely, but they appear to do so, judging from stuffed specimens. The pterographical characters of the Limicole, if we start with the Plovers as the representative of the Order, nearly approach those of the Pigeons. The principal difference lies in the fact that the proximal or backward overlap that characterizes the lowest two, or three, rows of median coverts in all the Desmognathz, and that is so nearly absent in the Pigeons, is again represented more or less perfectly in the majority of the Limicole. ‘The distal overlap of all the feathers next the manual region of the wing, that serves to dis- tinguish the Pigeons from the Galline, is a well-marked and constant feature in all the Limicole. There is one group‘of feathers, firm on each edge, that extends backwards from the carpal joint down to the greater wing-coverts ; on the distal side of this the median coverts all overlap towards the margin of the wings on that side, up to the alula, while on the proximal side of the same firm-edged feathers the median coverts overlap in the opposite direction as far as the point where they are met by that of the proximal area, which, again, lap forward. It is difficult to convey an exact idea of this somewhat complex arrangement except by means of a diagram, such as that of the wing of Gallinago celestis, fig. 22, p. 198, which well exemplifies the style current throughout not only all the Limicolz, but throughout nearly all birds with a Schizognathous palate. Variations of a minor character occur within the limits of this Order. Even in the case of two birds so closely related as the Common Snipe and the Woodcock (figs. 22, 23), such differences may be detected. The Snipe follows the normal Limicoline style, while that of the Woodcock more resembles aberrant forms such as @dicnemus, which comes nearer to the Bustards. I was so much struck with the difference alluded to, that I sought for evidence of a deeper-seated and more reliable nature, with a view to getting further information upon this point. Such differences do exist, notably in the structure of the skull; but I have not yet had an opportunity of following 198 MR. J. G. GOODCHILD ON THE * (Apr. 6, the subject far enough to speak with confidence in regard tu other differences noticed. Fig. 22. Fig. 23. Gallinago, Scolopax, From the central forms of the Limicolz nearly all the modifi- cations of style observable in the Carinatz could be traced without difficulty ; and the forms now remaining to be considered join on naturally enough to such types as that represented by the Plovers. In one direction, and at no remote distance from the Plovers, we come to the Rails, represented in fig. 24. In another direction, Rallus. Sterna. gradations equally gentle conduct us to the Gulls and the Terns (fig. 25). Along another line of modification we arrive at the Cranes. The Storks again stand at no great distance. Each of the forms here mentioned, in turn, leads to others more distantly removed from the central type. Beyond the Gaviz lie the Pygopods, represented by Alca (fig. 26). These in turn graduate easily into the Tubinares, as represented by Puffinus and by Diomedea (fig. 27). Closely resembling these last in style of wing-coverts follows Sula (fig. 28) and Fregata (fig. 29), which lead the way to one of the extreme modifications of style observable in this particular, ex- emplified by Plotus (fig. 30). Starting from another point, the CUBITAL COVERTS OF BIRDS. sang Se cul SS SESS SUAS RE ae « ae THN et GOL Abe yh SS <— CUL GCE C US RS = OC RCS Se CURLS Vy we ee ‘ ae ~ SX 199 200 MR. J. G. GOODCHILD ON THE * [Apr. 6, normal Ciconiine pattern, represented by that of Dissura maguari (fig. 31), leads the way through Mycteria (fig. 32), to Leptoptilus Disswra. Mycteria, (fig. 33), whieh, in respect of the feature under consideration, stands midway between the Ciconiine birds and the Tubinares. Between the style of the median cubital coverts in Leptoptilus and that of Fig. 33. LUGE a \ ACRES Brera, 1} rit WLS t poe SNE CREST So eaa SORA ae Leptoptilus. the Cathartide (fig. 34), I have hitherto failed to detect any difference of importance in respect of the feature specially under notice. So far as the imbrication of the wing-coverts is concerned, Leptoptilus and the Cathartidee might even stand im the same family. How far the purely superficial feature at present speciaily under notice can be regarded as affording data of any value in corroborating the view advocated by Messrs. Garrod and Forbes that there is a close genetic affinity between the Storks and Petrels on the one hand and the Cathartide on the other, must be left to competent zoologists to judge. After a careful examination of living specimens of Diomedea, Ossi- Sraga, Puffinus, Fregata, Leptoptilus, Cathartes, Sarcorhamphus, and 1886. ] CUBITAL COVERTS OF BIRDS. 201 Gypagus, I have been so much impressed with the uniform style of wing-coverts prevailing amongst this group, that it seems to me difficult to believe that their genetic relationship amongst them- selves is more remote than Forbes regarded it. I cannot, after many years’ observation of the facts referred to in this paper, help re- garding this similarity of style of wing-coverts in birds so different, both in outward form and in their mode of life, as presenting us Fig. 34. Sarcorhamphus. with a certain amount of evidence of the transmitted survival, in an unmodified form, of a mode of imbrication of epidermic structures that at some remote period in the genetic history of the common Sauropsidan ancestors of these birds played some really important part in the economy of the wearer. During the differentiation of such parts of the creature’s organization as were directly affected by the struggle for existence, other parts, not so affected, either changed at a slower rate, or else were transmitted from generation to generation hardly modified at all. Habit, or mode of life, as birds now live, can at the most have played but a minor part in bringing about these diversities of style. We have but to compare the Swallows with the Swifts, the Sun-birds with the Humming-birds, and many other parallel cases, and we at once perceive that mode of life has had little or nothing to do with the origin of the features in question. The real cause lies deeper than that, and dates back far into the remote history of the Sauropsida. Reverting to the normal Ciconiine style of coverts, we find Platalea, with Jdis and its allied genera, differing but little from each other and from Ciconia. Tantalus, in this respect, stands nearer to the Limicole. The Cranes, again (fig. 35, p. 202), present another variation little removed from the central Pluvialine type. Somewhere near to the Cranes and the Storks, but connected in some way with the Gallinaceous style of coverts, stands the wing of the Secretary Bird (fig. 36, p. 202); it is quite unlike the true Accipitrine type. Proc. Zoou. Soc.—1886, No. XIV. 14 202 ON THE CUBITAL COVERTS OF BIRDS. « [Apr. 6; Lastly, come two birds whose wings I cannot refer satisfactorily to any one of the groups above described. One is the Osprey Fig. 35. No te SS AN eR ee Gk x v\ ys Grus. Gypogeranus, (fig. 37), whose wing seems to occupy an outlying position some- where between the style of the Pygopodes and that of the Accipitres. The other is represented by Pernis apivorus: several stuffed speci- mens of this bird showed the posterior row of cubital coverts lapping distally, somewhat as in the Ciconiine birds, and there were in addition some minor differences of less importance. Stuffed birds, at the best, afford data of a very untrustworthy character in this Pandion. particular ; but on laying my difficulty before Mr. Gurney, who had some Honey-Buzzards alive, he courteously replied by sending me from the Norwich collection a skin that showed the feathers disposed as they were in his own living birds. This agreed exactly with the style observable in the stuffed birds, and differed from all the other Accipitrine birds as herein limited. Perhaps the nearest repre- sentative style is that presented by some of the Peristeropods, as, for example, Craw. In regard to any conclusions connected with taxonomy that may be drawn from a study of the facts herein referred to there will probably be much difference of opinion. The facts themselves ma be, in general, easily verified by a careful study of healthy living 1886.] DR. GUNTHER ON A VARIETY OF FELIS LEOPARDUS. 203 birds, and most of the views admit, I believe, of no reasonable doubt. There can be little doubt, also, that up to a certain point there is a remarkable correlation of particular styles of imbrication of the cubital coverts with certain structural cnaracteristics—osteological, myological, visceral, and pterographical; so that, within certain limits, the disposition of the cubital coverts may be taken as a kind of index to the presence, or the absence, of deeper-seated characters whose importance in relation to taxonomy is generally recognized. Nevertheless, until the facts here called attention to have been in- dependently considered by other observers, I feel sure that it would be premature to press the importance of the bearing that any of these may seem to me to have upon taxonomic questions: for the present it will probably be generally deemed advisable to lay more stress upon the bearing of the facts upon the correct delineation of birds tor zoological purposes, than upon their value as furnishing addl- tional data as subordinate factors in any scheme of classification.” 4. Second Note on the Melanotic Variety of the South- African Leopard. By Dr. A. GUnruer, F.Z.S, {Received March 26, 1886.] By the last South-African mail I have received from Mr. N. Abraham, President of the Graham’s-town Natural History Society, a letter with photograph enclosed, which gives more positive infor- mation about the variety of the Leopard of the district of Albany, mentioned by Mr. Trimen in Proc. Zool. Soc. 1883, p. 535, and described by myself, ébid. 1885, p. 243, pl. xvi. The skin in Mr. Abraham’s possession leaves hardly any doubt that we have before us a case of incipient melanism, which, if the family in which the melanotic tendency showed itself had been left undisturbed, might have been developed into as complete a condition of melanism as is occasionally found in the Asiatic Leopard. Mr. Abraham writes as follows :— “ Graham’s-town, 8. A., March Ist, 1886. “To Dr. A. Ginther, F.Z.S8. « Dear Srr, “Knowing that you are interested in the black variety of Leopard found in the district of Albany, I write to tell you of a beautiful skin which I have in my possession and also to send you a photograph of the same. I had the flat skin photographed on purpose that I might send you a copy, as I thought a photo would convey'a good description and save many words. It will, however,’ be necessary for me to say that the blackness of the skin is more dense than appears in the photo. The gloss upon the skin prevented the photographer from giving a true idea of the beautiful black, which is dense in many parts. here are no rosettes or spots at all on the larger portion of the skin ; in this the photograph is quite correct. 14* 204 DR. GUNTHER ON A VARIETY OF FELIS LEOPARDUS. [ Apr. 6, The spots do not even show through the black as in the black Leopard of Java. The tail has had its point taken off; this accounts for its shortness. “The measurements of the flat skin are as follows :—Head and Flat skin of Felis leopardus, var. melanotica. body 4 feet 1 inch; portion of tail 1 foot 4 inches; distance from fore toes to central line of back 2 feet 3 inches. On the black portion of the skin the hair is short with a very thick underfur. The tail is not black, but very dark, and has a somewhat remarkable appearance. The markings on the front legs differ very much from the markings on the hind legs, being very tawny with 1886.] ON OVIS HODGSONI AND OVIS VIGNEI. 205 scarcely any dense black, while the hind legs are slightly tawny with elear markings of black and white. The whole skin is very handsome and remarkable. The specimen was caught by a native in a trap and then shot. The native took the tip of the tail and the claws for trophies. It was caught about twenty miles from Graham’s-town. I have made many inquiries respecting this peculiar variety with the hope of forming some good theory explaining this deviation from the ordinary type. I ean only trace four specimens, viz. :—The skin in the Graham’s-town Museum (this is a good specimen, but not nearly so black as the one in my possession); another was taken to England by Mr. Bowker, and is in the British Museum; a third was sold some time ago at a Church bazaar, but I cannot trace it; and the fourth I have. I do not know of any other for certain. All these have been shot in, or about the same district. The one I have came from Collingham near to Graham’s-town. I am told that there are two living specimens still in the district, and there may be more, but these two have been seén, but not captured. I am still on the trail for more information ; at present I cannot give any certain or probable account of the origin of this variety, but I write this to you and shall be glad to forward you further information when I have completed my investigation. *T yemain, dear Sir, Yours sincerely, (Signed) Nenpick ABRAHAM, Pres. Graham's-town Natural History Society.” Apnil 20, 1886. Prof. Flower, LL.D., F.R.S., President, in the Chair. Mr. O. Salvin, F.R.S., exhibited a living specimen of an exotic Worm—Bipalium kewense (Moseley, Ann. & Mag. N.H. ser. 5, vol. i. p- 238), found at Hawksfold, Fernhurst, April 19, 186, amongst the broken tiles at the bottom of a pot of Calceolarta, which had been in a cold frame the whole winter. This fact suggested that the true home of B. kewense was some temperate region. The following extract was read from a letter addressed by Mr. R. A. Sterndale, F.Z.S., to Sir Victor Brooke, concerning a case of hybridism between Ovis hodgsoni and O. vignei :— ‘In the mountain-range south of the Indus, near Lanskar (the precise locality being for obvious reasons withheld from publication), a herd of Ovis vignet were observed for some years to contain a large ram of Ovis hodgsoni, who drove out the weaker Shapoo rams and appropriated the ewes of the herd. The ram was ultimately, one winter, killed and eaten. by Chankos or Tibetan wolves; but during his stay he produced a family of hybrids possessing greater size of horn and head, with characteristic colouring combining traits 206 MR. J, B, SUTTON ON DISEASES OF “Apr. 20, of both animals. In course of time these hybrids were crossed again with Ovis vignei, and the third generation shows signs of degene- ration from the larger sheep and of reversion to the type of O. vignei. «The skull of the half-bred animals, which the Tartars called Nyan Shapoo, the former being the name of the Ovis hodgsoni or Ammon, and the latter that of the Ovis vignei, is nearer in size to Ovis hodgsoni, which is double that of the other. The horns of these hybrids are rounded in front, resembling what has been figured of Ovis brookei, but hollowed out behind like those of O. vignetz. The horns of the quarter-bred animal are square in front and hollowed behind like the true Shapoo-type, but are more massive than the pure- bred Shapoo. “* Now as regards the colour of the skin, the Nyan or Ovis hodgsoni has no black beard or throat-stripe, which O. vignei has. The half- bred animal shows no black, but the quarter-bred does in a modified but decided degree. The half-bred turns also in summer to the colour of O. hodgsoni, having more of a blue-grey or lavender tint and less of the fawn colour of O. vignei; with the white throat of O. hodgsoni, it also gets the dark patch at the side of the neck. The skin of a quarter-bred specimen before me is of a bright fawn above, sides and rump white, and a black stripe down the middle of the throat.” Sir Victor Brooke was of opinion that Ovis brookei, Ward, P. Z.S. 1874, p. 143, was probably established on a somewhat similar hybrid. The following papers were read :— 1. On some Specimens of Disease from Mammals in the Society’s.Gardens. By J. Buanp Surron, F.R.CS., Erasmus Wilson Lecturer on Pathology, Royal College of Surgeons, Lecturer and Assistant Surgeon to the Middlesex Hospital. [Received March 30, 1886.] During the past twelve months several specimens illustrating diseases of mammals in the Society’s Gardens have come to hand. Some of them present features of such exceptional interest that it is desirable they should be placed on record. Of the value of the systematic examination of the bodies of wild animals dying in the Scciety’s Gardens there can be no doubt whatever—not in the sense that it will enable us to deal with diseases occurring in them, but in the amount of light likely to accrue to pathological science in general if the investigation be carried on with the diligence and care its importance demands. The specimens to be described in this paper are of value, inasmuch as many of them are somewhat rare in 1886.] MAMMALS IN THE SOCIETY'S GARDENS. 207 their nature, whilst others illustrate pathological conditions not before described in wild animals. In 1877 Mr. Garrod read a short paper before this Society ‘‘ On the Mechanism of the Intervertebral Substance, and on some Effects of the Erect Position of Man” (P. Z. 8. 1877, P. 50) from which the following extract has been taken :— “The assumption of a vertical attitude by a creature originally differentiated for a horizontal position of its body, has produced but marvellously slight inconvenience. If it had resulted in many, man could scarcely have survived. There are one or two, however, which are most clearly traceable to this cause, including the painful tendency to prolapse, antiflexion, and retroflexion of the uterus in women, as well as crural hernia in both sexes, and inguinal hernia in the male,” At the time the preceding paragraph was written, little was known, and far less recorded, concerning the abnormal conditions referred to by Mr. Garrod. The unusual opportunities which have occurred to me during the past five years of investigating diseases of wild animals will render necessary a reconsideration of this opinion. In the first place prolapse of the uterus occurs with tolerable frequency, not only in domesticated mammals, but in the lioness, tapir, Cape hunting-dog, the pygmy hog, deer, antelope, and others. These examples are sufficient to show that it is not entirely attribu- table to the erect position. With regard to flexions of the uterus, it is a remarkable fact that no fewer than one fourth of all the female Monkeys dying during the past two years presented extreme examples of this abnormal con- dition of the organ. In many the displacement far exceeded any- thing that I have seen in the human female. Well marked speci- mens of flexion of the uterus occur also in Deer. (For a detailed account of these cases and their etiology consult Path. Soc. Trans. vol. xxxvi. p. 502.) The frequency and severity of the cases show that the flexion is due to causes in addition to the erect position. Concerning hernia, it has always seemed to me strange that Man, whose inguinal canals are, in the ordinary course of events, more or less obliterated, should be so liable to visceral protrusions at these spots, whilst Monkeys, in whom the inguinal canals in most species remain more or less patent, should escape. It is certain that Horses are liable to inguinal ruptures; and I have long known that the same defect occurs with tolerable frequeney in Sheep. During the past two months I have been so fortunate as to meet with two cases of inguinal hernia in Monkeys. In the first, Macacus cyclopis, a large | plug of omentum occupied the funicular pouch of the left side ; the second occurred on the right side in a Macacus sinicus, The details of the condition may be gathered from fig. 1, p. 208. This Monkey had also a large varicocele on the lett side. These. specimens are sufficient to show that such abnormalities are not peculiar to Man. Probably most individuals among the civilized races of mankind 208 MR. J. B. SUTTON ON DISEASES OF fApr. 20, suffer at some period of their life from those troublesome thickenings of the skin of the feet and toes known as corns. Structurally a corn consists of thickening of the epidermis, due to pressure of an intermittent character, often the result of badly fitting boots. In many cases a small sac containing fluid may be detected between the thickened epidermis and the deeper tissues ; this sac is techni- cally termed a bursa. In others the bursa is replaced by loose connective tissue which allows the corn to glide freely over the underlying structures. We find excellent examples of corns in the ischial callosities of the Cynomorpha and in the callous pads found on the feet of Carnivora. The right funicular pouch of peritoneum of Macacus sinicus, occupied by a plug of omentum, 0; the testis, 7. Of late years the attention of surgeons has been directed to corns, in consequence of a very remarkable affection to which they are able. Under certain abnormal conditions of the spinal cord and peripheral nerves, such as locomotor ataxy, sclerosis, and peripheral neuritis, the corus ulcerate, and at last the ulceration perforates not merely the corn, but the whole thickness of the foot; hence it is now familiar as the “ perforating ulcer.” It was to me a matter of no small interest to find the callous pad on the foot of a Civet Cat the seat of a perforating ulcer; the interest was considerably heightened when, on opening the spinal OL ee | 1886. ] MAMMALS IN THE SOCIETY'S GARDENS. 209 canal, the cord was found soft and almost diffluent. By careful hardening and manipulation, sections were obtained from the cord and submitted to the microscope. It exhibited a most marked degree of sclerosis. This was also seen in the nerves of the affected limb. The animal was supposed to be about seven years of age, and had been paralyzed for some time before it died. The specimen was shown to a number of experts, who were unanimous as to the nature of the affection, viz. perforating ulcer, with sclerosis of the cord and nerves. I then ventured the opinion that more cases would come to hand, A few weeks later a second specimen came under my observation, also in a Civet Cat; and, lastly, a most interesting example in the Two-spotted Paradoxure (Nandinia binotata). In the case of the Paradoxure the affection of the callous pads is in an early stage, for the ulcers, one on each foot, are as yet shallow (fig. 2). Perforating ulcers (w) in an early stage affecting the feet of a Paradoxure, Nan- dinia binotata, secondary to sclerosis of the spinal cord. The ulcers were perfectly symmetrical on the fore and hind feet. F, the fore, and H, the hind foot. The most remarkable feature in the specimen is the perfect symmetry observed in the ulcers; in each fore foot the position and shape of the sores correspond exactly, and this is also to be observed in the hind feet. In this case only the lumbar and anterior portion of the spinal cord could be examined ; for, after the animal died, its com- panion, much to my annoyance, had eaten the middle portion of its 210 MR. J. B. SUTTON ON DISEASES OF FApr. 20, back. However, an examination of such pieces of the cord as remained showed well-marked and indisputable sclerotic changes. In 1842 Sir James Paget and Dr. William Budd’ almost simul- taneously directed attention to the frequent symmetry exhibited by disease of the tissues of the body. For example, an eruption on the skin of one leg is occasionally imitated by an eruption on the opposite leg, symmetrical, not only in position, but often in the shape of the patch, in the grouping, and even in the number of spots in each group. This symmetry is not merely confined to skin eruptions, but to diseases of the joints, sense-organs, nerves, bones, tumours, &c. Examples of symmetry occur very frequently in animals as a result of disease; and the following cases will serve as striking instances. In the accompanying drawings (fig. 3) will be seen the scapula Fig. 3. Examples of symmetrical exostoses (c) in the skeleton of a Monkey, affecting the scapula, great trochanter, and coracoid process. The tumours on the opposite side were exactly similar in shape and situation, and nearly equal in size. : and femur of a Bonnet-Monkey that died of bronchitis complicating rickets. The inferior angle of the scapula is occupied by an osseous tumour containing tracts of cartilage. The base of the coracoid process presents a rounded projection, which would probably have grown into a tumour had the Monkey lived. The great trochanter of the femur presents also a rounded tumour similar to that of the scapula, but containing less cartilage. Each humerus presented a 1 Med.-Chir. Trans. vol. xxv. —y es I Re | é Perincl x: 1886. ] MAMMALS IN T'1E SOCIETY’S GARDENS. 212 curious deformity, for at the junction of the upper and middle third the shaft was bent almost at a right angle. The corresponding bones of the opposite side presented precisely similar lesions. The sebaceous glands of the skin very frqeuently in the human subject suffer obstruction of their excretory duct. The result is that the gland continues to secrete, but the outlet being closed, the sebaceous matter accumulates until at last a definite swelling results, which may remain of insignificant proportions, or attain a diameter of two or three inches in exceptional cases. Technically such swellings form one of a group known as “ retention cysts.” The museum of the Royal College of Surgeons possesses some specimens of symmetrical sebaceous cysts growing from the wings of Wood-Pigeons. The specimens were presented by Mr. Tegetmeier. It appears that in certain seasons a large number of birds are found with swellings such as these on the wings, legs, and feet. A Cockateel, Culopsitta nove-holiandie, with symmetrical sebaceous cysts on its wings, An excellent example of this affection has recently come under my notice in a Cockateel, Calopsitta nove-hollandie. In this pretty bird there has developed on the inner surface of each wing a seba- ceous cyst. The position, size, and shape of the ‘‘ swelling’ in the two cases exactly correspond, as may be seen on reference to the drawing (fig. 4). The specimen serves as an excellent illustration of symmetrical disease. Malformations are frequently as symmetrical as tumours and skin eruptions. Mr. Forbes has recorded in the ‘ Proceedings’ of this Society (1882, p. 442) an example of webbed fingers in a Pitheci« satanas. ‘*The third and fourth digits of the manus on each side were completely connected down to their tips by a fold of nude skin, with their nails closely apposed, though not connected, along their 212 MR. J. B. SUTTON ON DISEASES OF [-Apr. 20, contiguous margins; the remaining digits were normal.” I[ re- member examining the specimen, at the time Mr. Forbes noticed it, in the Prosector’s room, and was impressed with the perfect sym- metry of the malformation. Since then one other example of malformation in the manus of a Monkey has occurred. A Gibbon (Hylobates leuciscus), which lived in the Gardens a few months, was found to have a supernumerary finger on each hand. In this case the additional fingers possess a metacarpal bone which was attached to the ulnar side of the meta- carpal of the fifth digit, and it seems as though the supernumerary bone was formed as a result of bifurcation of the distal end of the fifth one. The carpal bones do not present any abnormality. So few examples of polydactyly in Quadrumana have been noticed that the case before us is worthy of record. Fig. 5. A follicular cyst from a Prehensile-tail Porcupine, Sphingurus prehensilis. The upper figure represents the jaw after the remoyal of the cyst. w, the inferior dental nerve. The lower drawing is the cyst with the teeth projecting into it. The arrow marks the position of the mental foramen. As an additional illustration of symmetry in disease, the following ease is of value. A Prehensile-tailed Porcupine died from the effects of a large abscess on each side of the mouth. These had burst externally, giving rise to deep sinuses. A probe passed into each gave evidence of necrosed bone; and at first sight the case seemed to be one of alveolar abscess consequent upon diseased teeth, a condition of things exceedingly common in animals. On examining the mouth I failed to find the lower incisors; this was very sin- gular, because the bone at the symphysis was quite normal. On tracing one of the sinuses by dissection, it was found to lead into the mental foramen, and thence into a cavity occupying the body of 1886. ] MAMMALS IN THE SOCIETY'S GARDENS. 213 the inferior maxilla. This cavity was filled with pus, but the abscess was limited by fibrous walls of considerable thickness. Feeling con- vinced that this was something more than a simple abscess, the bony walls were dissected and the sac removed and examined in detail. This cyst is represented of natural size in fig. 5. Projecting into its posterior aspect are portions of the fangs of two undeveloped teeth. This is sufficient evidence to show that we have to deal with a follicular cyst—that is, the walls of this sac are constituted b * the greatly distended follicle of one of the teeth, probably the incisor. From some cause or other suppuration had occurred, and led to the necrosis of the maxilla and absorption of the fangs of the The tunica vaginalis and testis of a Lamb affected with a congenital parenchymatous hydrocele. c, cremaster; d, tunica albuginea; e, epididymis; ¢, secreting-tissue of the testis. molar teeth: a remnant of one may be seen projecting into the cyst. The inferior dental nerve, as a mere thread, was closely embedded in the walls of the jaw on the outer side of the sac. The opposite maxilla was affected in a precisely similar manner. The last example of symmetrical disease I shall describe in this communication is a singular affection of the testes of a Lamb, which, so far as my knowledge of testicular disease extends, is unique. The lamb was thought to be ruptured on both sides, but on cutting into the supposed hernial sac a large quantity of fluid escaped, but no gut or omentum were found. The remaining testis was removed entire with its coverings and sent to me. The enormously dis- t ended outer covering (fig. 6) is the tunica vaginalis and testis cut off 214 MR, J. B. SUTTON ON DISEASES OF [Apr. 20, from its connection with the peritoneal cavity. A few fibres of the cremaster muscle are spread over its upper limits. Inside this, and in close apposition with its walls, is the tunica albuginea, greatly distended, with the epididymis stretched over it like a strap. On . cutting into it, a pint of straw-coloured fluid escaped. This liquid was alkaline in reaction (sp. gr. 1020), and contained one half its volume of albumen. The substance of the testicle presented a very remarkable appear- ance, for it looked like the roots of a tree in. miniature. There was a central main stem, and from it slender rounded rootlets composed of - testicular substance, 7. e. seminiferous tubules and connective tissue, passed outwards to the sac-walls. ‘The appearances were the same in both testes. The condition is best expressed by saying that it resembled a hydrocele, except that the fluid was within the tunica albuginea instead of in the cavity of the tunica vaginalis. The occiput of an Ichneumon, with dislocation of the atlas and subsequent ; ankylosis of that-bone to the occiput. The specimen has been brought before the notice of the Society, with the hope of inducing others who have opportunities of seeing similar cases to place a description of them on record. In 1879 Prof. Flower gave an account of a very remarkable con- dition presented by the occiput of a Beluga. In this Whale the atlas had become dislocated from the occipital condyles, and dis- placed in such a manner that the passage for the spinal cord at the foramen magnum had become reduced to a very narrow chink, only three quarters of an inch in transverse measurement. The Whale had survived the accident some considerable time, for the displaced ee a oe a a a ao a ee 1886. MAMMALS IN THE SOCIETY'S GARDENS. 215 atlas had become firmly ankylosed to the occiput, and it is very curious that the animal could have survived so serious an accident. A somewhat similar case came under observation in an Ichneu- mon. In this instance the atlas had been dislocated from its rela- tions to the occiput and axis, so as to occupy the situation shown in the accompanying drawing (fig. 7). In this instance the animal must have survived the injury a long time, because the occiput and atlas are firmly united by new bone. Concretions formed of insoluble or indigestible matters are of frequent occurrence in the alimentary canal of Horses and Cattle, and at times may attain to very large size without causing any incon- venience. ‘This is more particularly the case when these zgropiles, as they are termed, occur in the ceecum of horses. In this situation they have been known to weigh more than fifty pounds. These heavier masses are composed of magnesium phosphates ; the lighter ones consist of hair which the animal licks from its body. This forin is fairly frequent in calves, and I have met with a specimen in a Hyena. Concretions of insoluble substances, such as magnesia, pins, seeds, &c., occur also in the human subject. Recently a Tiger died in the Gardens, and its bowels were found empty until the rectum was reached. Here a large mass of solid material was found about two inches from the anus, measuring six inches in length and eight inches in girth, covered with mucus. The lower end was bluntly pointed, and had caused by its pressure ulceration of the mucous membrane. The rectum was much dilated. On breaking into the mass it was found to be composed entirely of sawdust, which the animal had licked from the floor of the eage. A cast of the abnormal mass was taken at the time by the assistant, Mr. Ockenden. During the past four or five years there is one fact more than any other which has impressed me in the course of my work at the Gardens, and that is the infrequency of neoplasms. In the many hundreds of animals coming under observation, a tumour has been a rarity, and this applies with still greater force to cancers. The only example of this terrible malady I have seen in wild animals was a medullary cancer in the viscera of a Python. ‘The infrequency of these growths makes the following case additionally interesting. A Short-headed Phalanger, Belideus breviceps, was found to have a large, hard nodular mass in its marsupium. On slitting open the pouch a tumour presented itself, having the appearance represented in fig. 8, p. 216. Microscopically it presented all the characters peculiar to scirrhous cancer as seen in the human subject—that is, there were alveolar spaces enclosing masses of cells. ‘The alveolar walls were composed of dense fibrous tissue. The structural details of the growth coincided with that of the gland from which it originated, except that the cells, instead of clothing the walls of the alveoli in a regular manner, were tumbled in confusion into the interior. This case is, so far as I know, the first authentic example of cancer in a marsupial. The last specimen on my list is perhaps as interesting as any. It is an intussusception of the ileum into the cecum, through, but not 216 MR. J.B. SUTTON ON DISEASES IN MAMMALS. [Apr. 20, carrying with it, the ileo-czecal valve (see fig. 9, p.217). The invaginated portion measures two and a half inches. The portion of gut above the constricted portion was very congested and almost gangrenous. ‘The intussusception was very acute, and probably killed the animal, a Lemur, very quickly. The case is further interesting, for the intussusception occurred at that part of the intestine which Fig. 8. p> pos! O00) oe 2 Ay 2, o, 4 mr The marsupium of a Short-headed Phalanger, Belideus breviceps, opened order to show a scirrhous cancer growing from the mammary gland. n The microscopic characters of the growth are shown in figure B. is most frequently affected in this way in the human subject; but it is an example of the rarer form that occurs in this situation, viz. the ileo-czecal variety. The investigation into disease, structural aberrations, and mal- formations of animals is of considerable importance apart from its intrinsic interest. Darwin, in his ‘ Descent of Man,’ 2nd ed., 1874, page 6, writes :—‘ Man is liable to receive from the lower animals, and to communicate to them, certain diseases, as hydrophobia, variola, glanders, syphilis, cholera, herpes, etc. ; and this fact proves the close similarity of their tissues and blood, both in minute structure and composition, far more plainly than does their com- parison under the best microscope or by the aid of the best chemical analysis.” He then quotes Rengger to the effect that the Cebus azare in its native land is liable to catarrh, apoplexy, inflammation of the bowels, and cataract. This quotation seems to indicate beyond doubt that, had sufficient evidence been forthcoming regarding diseases of animals, Darwin 1886.] DR. O. FINSCH ON A NEW WILD PIG. 217 would most certainly have taken them into account as arguments in favour of his doctrine of Evolution. So far as my own observations have extended, and each month adds new facts, there seem to be few forms of disease peculiar to Fig. 9. Tleo-cecal intussusception in a Lemur. ¢, colon; 7, ileum. Man. On the other hand, certain affections occur in some animals with much greater frequency than in him, whilst a few diseases are entirely confined to them; many are also modified by peculiarity in structure, mode of life, and environment of the affected animal. 2. On a new Species of Wild Pig from New Guinea. By Dr. O. Finscu, C.M.Z.S. &c. [Received March 22, 1886.] The second species of true Sus from New Guinea is a very distinct one, and may be separated at once from the well-known Sus papuensis by the following characters :— Sus NIGER, sp. nov. Uniform blackish, even when young. These characters are sufficient, in all ages, to separate the present species from Sus papuensis, which is quite different, being in the adult brown, with a very distinct light-coloured mystacal stripe and legs, while the young is rusty brown with light rusty-yellow stripes, as inour Wild Boar. Proc. Zoou. Soc.—1886, No. XV. 15 218 MR. A. S. WOODWARD ON THE MANDIBULAR [Apr. 20, I was fortunate enough to bring home living examples of both these species, which are now deposited in the Zoological Gardens at Berlin. The specimen of Sus papuensis was obtained in the month of May, on the north coast of New Guinea, near the place noted on the charts “ Passir Point,” a point, however, which does not really exist ; it was then striped, but has now changed to the coloration of the adult animal. The Black Pig (Sus niger) I purchased at Hihiaura, a village some miles east of Bentley Bay; it was then very young (perhaps six weeks old), and of a uniform black colour, which it still retains. Sus niger is scarcer than Sus papuensis, but lives in the same localities ; it is of a more slender figure, higher on its legs and has a much longer head. It grows to a considerable size, and I have seen very huge animals of this species. I have observed Sus niger in a domesticated or semidomesticated state everywhere I have been in New Guinea along the south-east coast, and on the north-east coast from Milne Bay to Humboldt Bay, but always less common than Sus papuensis. The natives catch the young ones and feed them; they are pets of the women and often nursed at their breasts, and get very tame. This is the reason why it is so difficult to get them. I have seen some very large specimens in Hood-Bay district (village Kerapuno). Along the north-east coast I saw this species in all the native villages, especially in Chads Bay, in Village Island west of Fortification Point, in Astrolabe Bay, and in Humboldt Bay. It may be mentioned that along this coast I never saw any imported domestic pigs, but such pigs have been introduced into the Port-Moresby district and other piaces where missionaries have been sent. The only specimen of Sus niger in a Museum that I know of is a young one in the Museum of the Hon. William MacLeay of Sydney. 3. On the Relations of the Mandibular and Byoid Arches in a Cretaceous Shark (Hybodus dubrisiensis, Mackie). By A. Smita Woopwarp, F’.G.S., of the British Museum (Natural History). (Communicated by the Secretary.) [Received March 23, 1886.] (Plate XX.) Exactly as in all other divisions of the Animal Kingdom, the rapid accumulation of morphological facts regarding the Selachian order is providing a sure basis for distinguishing the more archaic from the decidedly modern types. There can be no longer any doubt, for example, that among living Selachians the most primitive and ancient ferms are the Notidanide, the Cestraciontide, and the Chlamydoselachidee. And of all the characters by which these groups are definitely marked off from the remaining members of the Order, none are of greater interest and importance than those relating 1886.] AND HYOID ARCHES IN A CRETACEOUS SHARK. 219 to the cranium and the cartilages of the visceral arches. Employing the terminology of Prof. Huxley, published in this Society’s ‘ Pro- ceedings’ for 1876 ', it may be said that the skull in each of the three families just mentioned exhibits a nearer approach to the primitive amphistylic type than does that of any other adult living vertebrate, the hyomandibular taking very little share in the support of the mandibular arch, and the union of that arch by direct articulation with the cranium being only slight and sometimes almost wanting. The superinduced modifications in the Notidanide and Cestraciontidee are very evidently in the direction of an autostylic arrangement— the former having a postorbital articulation of the pterygo- quadrate, and the latter a more extensive preorbital connection ; and in the Chlamydoselachidee there are somewhat similar tendencies, although the great extension of the pterygo-quadrate cartilage beyond the chondrocranium has apparently rendered the hyoman- dibular support of some importance. It would seem, in fact, that the oldest representatives of the Selachian order had skulls which were neither hyostylic nor autostylic, though their least altered descendants incline rather to the latter type; and that Notidanus and Cestracion especially, with Chlamydoselachus in a less degree, afford some slight glimpse into the early condition of the mandibular and hyoid arches from which the two later modifications have developed. Such being the conclusions based upon a study of living Selachians, it becomes of especial interest to determine to what extent they are confirmed or otherwise by the evidence of fossils. The remaius of Sharks, Rays, and Chimeroids are abundantly scattered throughout most marine formations, from the Devonian to the latest Tertiary, and the biologist might thus be led to expect considerable information from this field of research. Unfortunately, however, “ the imperfection of the geological record”’ presents its accustomed difficulties, and almost all the facts hitherto discovered relate merely to such hard structures as spines and teeth. There are also a few instances in which the entire fish has been described in a general way; but Prof. Cope’s elaborate account~ of some cranial fossils from the Permian of Texas appears to be the only contribution of importance that has yet been made to the morpholog of the skull. Under such circumstances, I venture to offer to the Zoological Society a brief description of a Cretaceous fossil in the British Museum, which is particularly remarkable from the simi- larity of the archaic features it presents to those of the existing types already mentioned. The fossil in question (no. 41675 of the B.M. register) was ‘1, H. Huxley, “On the Ceratodus forsteri, with observations on the Classification of Fishes,” Proc. Zool. Soc. 1876, pp. 40-45. 2 B. D. Cope, “On the Structure of the Skull in the Hlasmobranch genus Didymodus,’ Proc. Amer. Phil. Soe. vol. xxi. (1884), pp. 572-590, with plate. See also further remarks by 8. Garman, “ Chlamydoselachus anguineus, Garm., a living species of Cladodont Shark,” Bull. Mus. Comp. Zool. Harvard Coll vol. xii. no. 1 (1885), pp. 28, 29. - 15 220 MR. A. S. WOODWARD ON THE MANDIBULAR — [ Apr. 20, obtained from the Chalk of Kent, and is in an excellent state of preservation. It agrees in all important respects with a less perfect specimen in the same collection, which forms the type of Hybodus dubrisiensis, Mackie '—this fossil having been placed with the Hybodents in the- Museum series by Mr. William Davies, and subsequently figured by the editor of the ‘ Geologist’ under the name just quoted. And it may be added that the teeth are undis- tinguishable in general character from those of the typical species of Hybodus of earlier date. The specimen (Plate XX.) exhibits the pterygo-quadrate and Meckelian cartilages of each side,"those on the right, however, being broken away for about the hinder third ; on the lett side, the two elements of the hyoid arch are well shown in their natural position, and less complete remains of the corresponding cartilages are also seen on the right. Teeth and shagreen granules are abundant, and three well-calcified vertebree appear at the back. The pterygo-quadrate cartilage (figs. 1, 2, pg) measures 0°073 m. in length, and varies considerably in depth at different points. At the anterior end it is comparatively low and somewhat folded inwards above, but it soon begins to deepen by the rising of the upper border, which rapidly ascends to form a pterygo-trabecular process (p); this is placed at about one third of the distance from the fore to the hinder extremity. The process is almost pointed, and posteriorly the upper contour at once fa!ls again to some extent, though soon re-ascending in the form of a gentle curve to a still higher prominence (0¢), which exhibits in front a very distinct, relatively broad articular facette. This occurs at about the end of the second third of the cartilage, and thus far the characters are shown on both the left and right sides of the fossil; but the hindermost third is only preserved to the left. A little beyond the summit of the facette, the upper border becomes thickened and turned outwards, and its edge forms a regular gentle curve down to the articulation of the lower jaw. The inferior border of the car- tilage is almost straight for its anterior two thirds, the dentigerous portion, and then there follows a curved hollowing ; next is a minute process, marking the commencement of the articular portion, which shows two small hollowings and a terminal convex condyle. The Meckelian cartilage, or lower jaw (mk), is preserved on both sides of the fossil, but is only perfect on the left. “It measures 0:0685 m. in total length, being thus somewhat shorter than the pterygo-quadrate. The upper contour is almost straight from end to end, only a slight hollowing being perceptible immediately beyond the termination of the tooth-bearing portion ; and this is sueceeded by a short, wavy articular edge, fitting into the corre- sponding irregularities at the hinder end of the pterygo-quadrate, and finally presenting a distinct concavity for the reception of the upper condyle. The cartilage is deepest just beneath the end of the dentigerous portion, from which point the lower border curves upwards both in frent and behind ; posteriorly the curve is at first 1 §. J. Mackie, “‘ On a new Species of Hybodus from the Lower Chalk,” ‘ The Geologist,’ vol. vi. (1868), pp. 241-246, pl. xiii. 1886.] AND HYOID ARCHES IN A CRETACEOUS SHARK. 221 gradual, but then very abrupt, while anteriorly the rise is much more uniform and produces a markedly tapering outline. Quite at the front, the cartilage has the appearance of being more robust than is the case further back; but this is perhaps chiefly due to the infolding of the lower edge for the production of a trough for the membrane bearing the undeveloped teeth. On comparing this form of mandibular arch with the various modifications observed among living Selachians, it is at once evident that none agrees so closely as that of the two genera of Notidanide. Heptanchus and Hexanchus', indeed, exhibit an arrangement that differs in no essential particular from that just described in the Cretaceous Hybodont. In both cases there is not only a well-developed pterygo-trabecular process—homologous (as shown by Prof. Huxley *) with the pedicle of the tadpole’s suspen- sorium,—but also a distinct postorbital prominence and articulation, corresponding to the otic process in the tadpole*. The mode of articulation of the lower jaw is also nearly identical in each case ; and though the fossil is at present much crushed, it requires very little careful study to discover that the hollows for the muscles for raising the mandible were quite as deep in the Cretaceous Shark as they are in the living genera under comparison; the upper border of the quadrate region, however, is much less thickened than in the Notidanida and agrees more closely with that of ordinary Selachians. Tn the hyoid arch, the upper or hyomandibular element (figs. 1, 2, hm, and fig. 4) is comparatively small and slender. Its length is 0°037 m., and the cartilage is considerably arched and flattened in what appears to have been an antero-posterior direction. The proximal extremity is imperfect, but was evidently somewhat expanded at its articulation with the cranium; this end is also slightly twisted with respect to the axis of the rest of the element. Just below the bend, the cartilage appears contracted a little when viewed from behind, but soon expands again, forming a_ blunt tuberosity (¢) on the side nearest the pterygo-quadrate ; and from this point it finally becomes gradually narrowed until its termination in the imperfectly-displayed articulation for the cerato-hyal. The cerato-hyal (figs. 1,2, ch) is 0°048 m. in length, and is com- pletely shown on the left side of the fossil, though somewhat mutilated at the distal end ; the lower part, however, is well preserved on the right. The cartilage is considerably arched in the ordinary manner, and is much Jess robust towards its upper end than in the rest of its length. Compared with the hyomandibular, it is remarkably stout. A little below the proximal end it becomes comparatively large and ' See figures by C. Gegenbaur, ‘“ Untersuchungen zur vergleichenden Anatomie der Wirbelthiere.—U1. Das Kopfskelet der Selachier,” pl. x. I am also indebted to the kindness of Mr. Howes and Mr. Martin Woodward for every facility for studying the beautiful preparations of Heptanchus, Cestracion, &e. in the Biological Laboratory of the Normal School of Science. * 1. H. Huxley, loc. cit. p. 40. * It is interesting to note that Prof. Cope’s Permian Selachian skulls already referred to also exhibit this character, 222 MR. A. S. WOODWARD ON THE MANDIBULAR [Apr. 20, is much compressed from side to side, the superior edge thus formed being well marked and sharp, but the lower appearing thicker (fig. 2a). About two thirds of the distance from the upper extremity a gradual twist in the cartilage renders the remaining portion com- pressed almost from above downwards, and it ends distally in a triangular expansion, well shown on the right. The terminal edge was evidently articulated to a basihyal of considerable size, but of this no trace has been preserved. At one third of its length from the proximal end, the cerato-hyal exhibits a prominent tuberosity on the lower border (fig. 2, fu). This appears to be situated opposite a point corresponding to the attachment of the mandibulo-hyoid ligament of living Selachiaus’: but Ihave failed to discover indications of any similar prominence either in Heptanchus or the other specimens and figures to which I have been able to refer. It evidently represents a muscular insertion, and one of no small importance. In Teleostean fishes, the well-developed genio-hyoideus arises from an equivalent point in the hyoid arch, and by its insertion at the symphysis acts as the main depressor of the mandible *. In the Selachii, however, the function is undertaken chiefly by the coraco-mandibulares arising from the pectoral arch, and a differentiated genio-hyoid appears to be wanting. The elabo- rate researches of Vetter * in regard to the myology of the jaws and branchial arches in Heptanchus and Acanthias can leave no doubt that the tuberosity in question is that deep insertion of the great constrictor superficialis muscle which becomes the origin of the genio-hyoid in higher fishes ; and its marked character in the Creta- ceous Hybodont may perhaps indicate that in this form the differen- tiation had already taken place to a certain extent. On the whole, the form of hyoid arch just described bears a greater resemblance to that of the Notidanide than to that of any other living family. It agrees in the fact that the hyomandibular and cerato-hyal are most contracted at their point of union, but the elements are somewhat stouter than those both of Heptanchus and Hezanchus. The type specimen of Hybodus dubrisiensis (B.M. 36908) is of somewhat smaller size than the fossil here described, and as its cartilages are apparently less calcified, it probably represents a younger individual. It is comparatively imperfect, and except in the characters of the teeth and the upper border of the pterygo- quadrate, it does not admit of any detailed comparison with the foregoing descriptive account. There are, however, unmistakable indications of an articular otic process, besides a well-marked pterygo- trabecular eminence ; and a small fracture shows the slight thickening of the overturned edge of the quadrate region (fig. 6). 1 W. K. Parker, ‘On the Structure and Development of the Skull in Sharks and Skates,” Trans. Zool. Soe. vol. x. p. 210, pl. xxviii. fig. 2. * R. Owen, * Anatomy of Vertebrates,’ vol. i. p. 206, fig. 155. * B. Vetter, “ Untersuchungen zur vergleichenden Anatomie der Kiemen- und Kiefermusculatur der Fische.—I ,” Jenaische Zeitschrift, vol. vii. (1874), pp. 403-458, pls. xiv., xv. Si... Te, see tee 1886.] AND HYOID ARCHES IN A CRETACEOUS SHARK. 223 A third fossil in the National Collection (no. 49032) also belongs to the same species, and exhibits the remains of the anterior portion of what was evidently a complete fish at the time of its entombment. It agrees in size with the specimen here described, and exhibits traces of the articular facette on the otic process, in addition to part of the left cerato-hyal with its characteristic lower tuberosity. Fragments of the shoulder-girdle are also preserved, and a portion of the base of the chondrocranium; and the vertebral column is shown for a length of 0°16 m., comprising about 33 well-calcified asterospondylic centra. Unfortunately, all indications of dorsal spines are wanting. As the typical Hybodonts range throughout the whole of the Mesozoic strata, from the Muschelkalk to the Upper Cretaceous inclusive }, and as it has teen found impossible hitherto to recognize more than one generic type—Hybodus—on the evidence of spines and teeth, it would be interesting to compare the modifications in the skull of H. dubrisiensis with the corresponding structures in earlier species. As yet, however, no information in regard to these has been published, and the only deposits that have yielded satisfactory specimens are the Lower Lias of Lyme Regis and the Wealden of Pevensey Bay, Sussex. Of such fossils the British Museum contains an unrivalled series, and I hope to attempt the elucidation of the more important of these on a future occasion. It must suffice at present to add that, though there are well-preserved pterygo-quadrates from both the formations mentioned, there appears to be none but the most uncertain evidence of an articular facette on the otic process in any; aud if this observation can he confirmed it will become of considerable interest when taken in connection with the fact, pointed out by Prof. Huxley *, that the postorbital articulation in the living Heptanchus is only acquired comparatively late in the development of the foetus. It is also inter- esting to note that one of the Liassic specimens (Brit. Mus. no. p340) exhibits traces of a persistent notochord, with the arches alone calcified, whereas in the Cretaceous torm it has just been shown that there are well-differentiated centra. The differences between the anterior and posterior teeth are likewise more marked in H.dubrisiensis than in any of the earlier species of which satisfactory remains are known. It would appear, indeed, that there is distinct evidence of specialization as the Hybodonts are traced through the Mesozoic period, and it is almost certain that future research in regard to structures other than teeth will lead to the subdivision of the multi- tudinous forms hitherto grouped under one generic name. ! Teeth indistinguishable from Hybodus, and originally described under this name, occur in the Carboniferous, but they have been proved to belong to a distinct genus, T'ristychius (IT. Stock, “ On the Structure and Affinities of the genus Tristychius, Agass.,’ Ann. & Mag. Nat. Hist. (5) xii. 1885, pp. 177-190, pl. vii.). There are also other Palseozoic Hybodontide, e. g. Crenacanthus, * Loe. cit. p. 44, fig. 9. 224 MR. R. COLLETT ON HYBRID GROUSE. ._ [Apr. 20, EXPLANATION OF PLATE XX. Fig. 1. Side view of jaws of Hybodus dubrisiensis, Mackie. pg, pterygo- quadrate; mk, Meckelian cartilage; p, pterygo-trabecular process ; ot, otic process ; Am, hyomandibular ; ch, cerato-hyal. (B.M. 41675.) . Under view of the same: ¢wv, tuberosity on cerato-hyal. 24, natural transverse section of right cerato-hyal. . Teeth of the same, twice nat. size. 4, anterior tooth; b, hinder tooth. . Hyomandibular of the same, back view. 7, tuberosity. . Restoration of mandibular and hyoid arches of Hybodus dubrisiensis. . Section of the upper border of quadrate region of pterygo-quadrate of type specimen of Hybodus dubrisiensis, showing thickening. Figs. 1, 2, 4-6 are of the natural size. bo Soe co 4, On the Hybrid between Lagopus albus and Tetrao tetrix, By Rozsert Corrert, C.M.Z.S. [Received April 1, 1886.] (Plates XXI., XXII.) Introduction, p. 224. Young plumage, p. 251. Distribution, p. 225. Sex, p. 232. Propagation in Norway, p. 226. Supposed parentage, p. 232. Diagnosis and Configuration, p. 227. | Other Hybrids of Lagopus, p. 256. Measurements of ¢ & Q, p. 228. Habits, p. 238. Colouring, p. 228. Food, p. 239. Winter plumage, p. 229. | Skeleton, p. 240. Summer plumage, p. 230. Introductory Remarks. The existence in Northern Europe of two kinds of natural hybrids amongst the Tetraonide was already known in the last century, and one form of these is rather common in the forests of Norway and Sweden, as well as in some other parts of Europe, being met with annually in many districts, where its hybrid character is, as a rule, well known tothe inhabitants. This is the “ Rakkelfugl,” the cross between the male of Tefrao tetrix aud the female of T'etrao urogallus. The male of this hybrid, which has been known since 1744", in colour more nearly resembles the cock of Yetrao tetrir than that of Tetrao urogallus, whilst the female in this respect is less charac- teristic and resembles the hens of both species. In shape its hybrid nature is indicated by the form of the tail; in size it is intermediate between both parents, so that both sexes are larger than the father, and the male is even larger than the mother. The other hybrid, the result of a connection between Tetrao tetrix and Lagopus albus, which is called in Norway and Sweden “ Rype- Orre,” is much rarer, and specimens are still desiderata in most museums. The origin of this hybrid, its habits, and its places of resort are as yet partially, if not wholly, obscure. Its winter plumage is the only one which is generally known, whilst the spring or summer plumage is all but unrecorded. 1 Kel. Vet.-Akad. Handl. Stockholm, 1744, p. 181. P.Smit lth. HYBODUS DUBRISIENSIS, Mackie 7 30 re) 1886. Pl XX 1886. ] MR. R. COLLETT ON HYBRID GROUSE. 225 I will therefore endeavour to recount the most important features which have hitherto been noticed concerning this hybrid, which, on account of its rarity, as well as its pretty and peculiar external appearance, is well suited to attract the attention of naturalists. The earliest account of this hybrid dates from the year 1788, as Sparrman at that time gave an illustration of it and briefly men- tioned it as ‘‘ Vetrao tetrix, mas, varietas” in the third issue of the ‘Museum Carlsonianum’ (pl. 65), without, apparently, having suspected its hybrid character. In 1795 this was first noticed by Sommerfelt (‘ Topographisk Journal for Norge,’ 14 Hefte, p. 50, Christiania, 1795), who described two specimens from the districts about Mjdsen in Southern Norway, which he regarded as a hybrid between Tetrao tetriv and Lagopus albus. From the description, which is comparatively detailed (see below), it is evident that the Specimens were males in winter plumage. Subsequently a male shot in Wermeland in Sweden in 1808 was mentioned and figured by Thunberg (Vet.-Akad. Handl. Stockholm, 1808, p. 195), and he also recognized its hybrid character. The first who gave a more detailed and elaborated description of it was Nilsson in his ‘ Ornithologia Suecica’ in 1817, and subsequently in his various editions of his ‘Skandinavisk Fauna.’ Since then it has been occasionally treated of in different works on the fauna of Scandinavia, and here its winter plumage has also been given on plates, as in Nilsson, ‘ I]luminerade Figurer till Skandinavisk Fauna’ (plate 5); Lindblad, ‘Svenska Jiigareforbundets nya tidskrift,’ vol. xi. plate 4 (1873); Sundevall, ‘ Svenska Foglarna,’ plate 34 ; and Lloyd, ‘Game Birds and Wild Fowl of Sweden and Norway’ (London, 1867), &e.? Distribution. The “‘ Rype-Orre”’ has hitherto only been found in Northern and North-eastern Europe, and is known from Norway, Sweden, and Northern Russia. According to a report which I have just received from Dr. Pleske (of St. Petersburg), these hybrids in Russia are not very unusual. Most of them are obtained in the game market; therefore no special information can be given concerning the localities in which they were procured. He believes that about eight specimens are at present preserved in the Museum at St. Petersburg, most of which are males in winter plumage. Dr. Meves, of Stockholm, informs me that in 1872 he saw two specimens in winter plumage in the Museum at Moscow, both males; whilst others, said to be females, were only partial albinos of the female Tetrao éetrix. Dr. Kolthoff, of Upsala, has also seen two male and one female Russian specimens. It is remarkable enough that as yet there is no proof of their occurrence in Finland ; for Mela says, “It has not been recognized ‘In the ‘ Zeitschr. fiir die gesammte Ornithologie, 2 Jahrg. 1885, p. 47, tab. iii. (Budapest, 1885), Herr Henke has figured and treated of a specimen from Archangel under the name of Tetrao albo-tetrix hybridus, fem. This specimen is clearly only a partial albino of 7. feria, fem. 226 MR. R. COLLETT ON HYBRID GROUSE. ._ [Apr. 20, with certainty in our land, but it must surely be found if more care- fully sought after” (‘ Vertebrata Fennica,’ p. 164, Helsingfors, 1882). In Sweden several specimens have been captured, most of them in the northern counties (Helsingland, Jemtland, Norr- and Wester- botten), but a few as far south as Dalarne and Wermeland—as a rule amongst the mountain-ridges of the districts adjoining Norway. Dr. Kolthoff has informed me ia a letter, dated Upsala, 7th March 1886, that, according to his knowledge, twelve specimens of this hybrid have been preserved in Sweden, of which the Upsala Museum possesses four (one male, three females). The Museum in Stockholm owns four, of which one is a female. Almost all were found, it may be said, accidentally, amongst the game which is forwarded during the winter from the northern counties to the towns for sale. Propagation in Norway. The first specimen preserved in any Norwegian collection was a male in winter plumage, forwarded from Rorés in 1837 to the late Prof. Esmark. Until 1870, hardly more than halfa dozen specimens were found or preserved in Norway, all of which were males obtained from the mountain districts in the southern part of the country (the provinces of Christianssand, Bergen, and Hamar); but during the years subsequent to 1870, 15 additional specimens have been obtained. Thus at least 22 specimens of this hybrid have been preserved in Norway during the last 50 years, among which only two were females. Almost all these have been obtained by the University at Christiania ; at present there are eleven specimens ‘mounted (amongst which are the two females), one skeleton, and two skins. A few specimens have been sent abroad, and two are preserved in the museum of Bergen. Of these 22 specimens I have personally examined 13 in the flesh, having myself found some in the game- dealers’ shops, while the others have during the last few years been presented to or bought for the museum. All the specimens were found in the southern districts of the country, with the exception of one, which was obtained in Saltdalen near Bodo, thus just within the Arctic Circle (65° N. lat.). The most southern specimen was caught in Sande, near the Christiania fjord (59° 35’ N. lat.). The greater number of the preserved specimens, both in Norway and Sweden, have been in their winter plumage. One reason for this is that the greatest capture of the Tetraonidze takes place during the winter months, for during the summer they are protected by the game-laws ; and another is that the hybrids previous to the assumption of their winter plumage so nearly resemble the young males and the hens of the Teérao tetriv that they are easily passed over unnoticed. In the winter, however, their plumage is so marked and peculiar, that this very seldom happens; but it is very probable that the greater number of individuals do not fall into the hands of naturalists, 1886. ] MR. R, COLLETT ON HYBRID GROUSE. 227 In giving the following account of the “ Rype-Orre”’ I have had an opportunity of examining, besides the Norwegian specimens, the four specimens which at present (March 1886) are preserved in the Museum at Upsala, and which, by the kindness of Prof. Tullberg and Dr. Kolthoff, have been forwarded to me for examination. Of these specimens one is a male, namely Thunberg’s individual of 1808 (see above), the other three are females. Besides these I have examined a fine male specimen in winter dress, captured in Wermeland (Sweden) in the middle of January 1886, which I found myself in the game-market at Christiania in February last. Diagnosis and Configuration, Tail slightly forked ; number of rectrices 18 ; toes semiclothed, the outermost joints bare ; claws longand broad; bill stout ; eyebrows covered with warts, and pectinated above. Colour of male in winter dress: white underneath, with black feathers on the breast and flanks; blackish above, with whitish edges on all the feathers. A white band through the eye, and a blackish beneath it. Tail-feathers black, tipped with white. The female in winter dress more or less whitish underneath ; the back, breast, and flanks (sometimes the entire lower surface) trans- versely banded with reddish brown and black, all the feathers with whitish edges. Tail black, faintly speckled with brown and whitish. Bill rather like that of Tetrao tetrix, strongly built, but the culmen is not so plainly ridged as in that species; its size in the male is nearly double of that of Lagopus albus. The side branch of the mandible strongly developed. Eyebrows covered with numerous small red warts, and with a fine- toothed ridge above. The height of the eyebrows is about half the diameter of the eye; the comb im winter specimens is not very high. [oie shaped like those of Lagopus, long and broad, and very slightly oblique, the immer edge being a trifle broader than the outer. They are less curved than in 7’. ¢etrix, and their colour is not so dark as in that species. Toes semiclothed with hair-like feathers, densely in winter ; the innermost joint entirely feathered, the middle one naked above, but clothed on the sides, the outermost quite bare. The bare portions covered with horny rings, on the sides with one or two series of rounded scales ; under these there is a toothed comb (as in Zetrao, unlike Lagopus). Hind toe short, as in Lagopus (proportionally much longer in Tetrao). Tail slightly forked, the outermost feathers very slightly bent outwards at the end, and (in the male) 12 to 24 millim. longer than the centralones. Its length is proportionally longer than in 7’, ¢etriz, and more like that of Lagopus. Under tail-coverts slightly shorter than the central rectrices (or 228 MR. R. COLLETY ON HYBRID GROUSE.“ _—_[Apr. 20, about one diameter of the eye). In ZLagopus they are still shorter, or one diameter and a half, in 7’. tetrix one or two diameters longer than the central rectrices. Male and Female.—Besides the markings and size the following differences occur between the two sexes—the tail of the female is nearly square, the side branches of the upper mandible are more developed, and the comb-like scales of the toes and the ridge of the eyebrows are considerably longer in the male than in the female. Measurements. Male. Total ’ Outer tail- Centre tail- length. Wane feather. feather. mm. mm. mm. mm. 1.... 470 242, 142 122 Gudbrandsdalen, 7 Dec. 1870. 2.... 480 238 147 ey. Saltdalen, Nordland, 30 Dec. 1871. eit 237 138 106 Gudbrandsdalen, 8 Oct. 1872. 4,... 508 255 142 125 Osterdalen, 5 Nov. 1872. 5.... 480 252 140 2 Gudbrandsdalen, (?) Noy. 1872. 6.... 499 245 2 130 Gudbrandsdalen, 28 Feb. 1875. Ufpere 0s: 232 146 124 Hadeland, 27 Dee. 1879. 8.... 480 235 135 115 Tolgen, 3 Nov. 1881. Cease eesele 235 140 118 Sande Pred, 9 Noy. 1881. 10.... 530 235 150 125 Roros, 10 Oct. 1882. Female. 11.... 423 205 127 97 Gudbrandsdalen, Jan. 1875. 12.... 425 205 118 100 Roros, 7 Oct. 1876. It will be seen from these measurements that the male has an average length of 490 millim., about equal to that of the female Tetrao tetrix (but with slightly longer outer tail-feathers). ‘The total length of the female is about 424 millim., being thus considerably less than the male; it is, however, somewhat larger than the male Lagopus albus. Colouring. Of the fourteen specimens of this hybrid at present preserved in the Museum at Christiania, one is a young bird of the year, on which the brown plumage almost entirely remains; four are young birds changing to winter plumage, the latter being predominant ; finally, are eight in full winter plumage, and amongst these are two females. Besides these there is one specimen (a male in winter plumage) exhibited as a skeleton, In winter plumage are also the specimens in the Bergen and Upsala Museums. The specimens at Stockholm are likewise, so far as is known, in winter plumage, or in the changing from autumn to winter. A long link in the series is entirely wanting in all these collections, namely—the spring plumage, which is probably unknown ; the summer plumage, which is in all cases known from 1886. } MR. R. COLLETT ON HYBRID GROUSE. 229 the description of a single specimen in an old treatise (see below) ; and finally the young in down, which is also unknown’. Winter Plumage. The winter plumage develops itself in Norway during October, and as a rule is completed by the latter half of the month. Whilst one or two of the males had not moulted the last autumnal feathers in the beginning of November, one of the females was in full winter plumage on the 7th of October. This, however, was not an accidental circumstance, but has its analogy in Lagopus albus, in which the change to winter plumage takes place more rapidly in the females, although they begin to change later than the males. The tarsus and toes are then fully clothed, and the naked outer half of the toes is completely hidden by the overlying hair-like feathers. The male in winter (Plate XXI. fig. 1) has the upper parts black with greyish-white, finely freckled edges to the feathers; the under surface is white, with an irregular black pateh on the breast which may be of greater or less extent, occasionally parted in the middle, or so small that there only remain a few black feathers. On the flanks a few black feathers are always present, but sometimes hidden by the white ones. The wing-coverts are chiefly white, speckled with brown. The wing-feathers are brownish black, finely speckled with grey ; the outer web of the primariesis white. A more or less conspicuous white band passes through the eye, and under this a similar black one (including in most cases, but not always, the chin), with narrow white edges to the feathers. The upper tail-coverts are black with broad white edges; under tail-coverts white. The tail- feathers are black with narrow white tips, which almost disappear on the outermost ones. The front of the tarsus is greyish. The eyebrows are bright red; their height 11 millim., of which the upper toothed ridge is 43 millim. Although the winter garb is remarkably similar in its general appearance in the different individuals, a slight variation in some details will always be found. In some the unspotted white parts are more extended than in others, while in others the black feathers are predominant on the flanks and abdomen. One of the specimens in the University Museum (Nov. 1881) was unusually dark, with a very large patch on its breast, nearly black scapulars, and numerous black feathers on the abdomen. The female in winter (Plate XXI. fig. 2) has the upper parts banded with black and yellowish brown, and whitish freckled edges to the feathers. The ground-colouring of the lower parts is white, each feather blackish at base ; the breast and flanks barred with yel- lowish brown and black, and edged with white. The wing-coverts are speckled with white, greyish brown, and rusty yellow; the wing- ‘A more detailed account of the different plumages I have given in * Videnskabs-Selskabets Forhandlinger, Christiania,’ 1872 (p. 238); and ‘ Nyt = ee for Naturvidenskaberne,’ vol. xxiii. 1877, p. 159, and vol. xxyi. 1881, p. 324, 230 MR. R. COLLETT ON HYBRID GROUSE. (Apr. 20, feathers are brownish black, finely speckled with grey. A whitish stripe passes through the eye, under this a brown one. The upper tail-coverts irregularly barred with black, greyish brown, and yellowish brown, with broad white edges. The under tail-coverts white, sometimes a few feathers banded with rusty. The tail-feathers are black, with the outer web speckled brownish grey or whitish, and white-tipped ; the centre pair entirely mottled. The front of the tarsus as in the male. Thus in winter plumage there exists this difference between the sexes, that those parts which in the male are black with white edgings to the feathers, are more or less mottled brown in the female, and instead of the male’s black spot on the breast the female has the breast barred with yellowish brown. Of the three females from Sweden which at present,are preserved in the Upsala Museum, two (Jemtland, Feb. 1886 ; Angermanland, Jan. 1861) are normal, and on the whole similar to the before-mentioned Norwegian specimens. The last is, however, rather light-coloured: thus the barred feathers on the flanks are quite covered with white ones, so that these portions seem to be unspotted; the throat likewise is snowy white. Both are young individuals; this is seen by their slender and unworn beaks. The third female (Jemtland, January 1885) was somewhat different, and very dark in colour, without any part of its abdomen being entirely white. This was an old bird, the beak coarse and well-worn on the edges and point. The ovary was (according to Dr. Kolthoff) plainly visible. On the rump several well-worn autumnal feathers with brown cross lines remained amongst the white winter feathers. Its essential peculiarities were as follows :— On the upper parts, wings, and tail normal, though intermingled with a somewhat stronger reddish-brown colour. The whole of the lower half from the beak to the rump evenly furnished with broad brown and black cross bands; a few feathers quite white, others had white edges. In other respects like the former ones. Size normal. Although this specimen was decidedly more darkly coloured under- neath than the others, its general characteristics in markings and shape were otherwise quite in conformity with them. Summer Plumage. The period in the spring at which the individuals begin to change their winter plumage is unknown. All the specimens which i have examined were captured in the months October to February ; and on a specimen in the Museum at Bergen, shot in Voss (Bergen Stift) about the Ist March 1868, there is yet no trace of spring plumage visible. Whilst the spring plumage of the Rype-Orre is as yet unknown, there exists one account of a specimen in its summer garb. In 1823 Mr. Sommerfelt, jun.', in ‘ Magazin for Naturvidenskaberne,’ 1 A son of the Mr, Sommerfelt who is mentioned above (p. 225) as haying for the first time brought to notice its hybrid character. 1886. | MR. R. COLLETT ON HYBRID GROUSE. 231 1 Aarg. 2 B. p. 71 (Christiania, 1823), described a specimen in summer plumage which he obtained from Thoten (near the lake Mjésen in Norway). From the size of this specimen it appears to have been amale. The statement is as follows :— (Male? in summer (July)). ‘‘Caput, collum, dorsum, pectus Tetraonis tetricis famine. Remiges primores et secundarie albe, plurium tectricum albe. Rhachis remigis 1"° fusca. Rectrices nigre apicibus albis, duabus mediis nigris ferrugineo-undulatis ea- ceptis. Cauda non forficata. Abdomen et femora ut in T. tetrice femina, modo pennis singulis albis ornata, Digiti sublanati. Mag- nitudo T’, tetricis feemine.” The colouring of the summer plumage thus generally resembles that of the Greyhen, but is distinguished by a few white feathers on the abdomen. The tail-feathers also differ from the winter garb in that the central pair are transversely banded with brown, Au inaccuracy has probably been made in describing the wings as white instead of “ whitish,” as in summer it is not likely that the white colour would be more extended than in winter; (and the description “ digiti sublanati”” contradicts the possibility of the specimen being a partial albino of the female Tetrao tetrix). Young Plumage. The plumage of the young is, as one might expect, mottled brown like both parents, but the upper parts remind one more of Lagopus albus, the lower parts of Tetrao tetriv. I found a single spe- cimen, a male, in this garb amongst a parcel of game from Oster- dalen (South-eastern Norway) in the autumn of 1880; it had been probably shot or captured at the end of September. The plumage of the young on the whole is still retained, but a few winter feathers have already appeared amongst the brown ; the wings and the outer tail-feathers are also new, and belong to the winter plumage, and thus present a striking contrast to the other mottled brown feathers. Young male in autumn (Plate XXII. fig. 1).—The upper parts mottled and banded by rusty yellow and black, almost the same as in the young of Lagopus albus, the cross bands being narrower and closer than in the young of TZeérao tetriz. In the longer wing- coverts there is a discernible light elongated patch along the quills. The tail-feathers, as in Lagopus albus, jun., are transversely banded with black and reddish brown. On its lower parts the breast and sides, as in the young of the Tetrao tetriz, are closely and evenly banded with black and rusty yellow, and both colours are about the same extent. In this respect they more nearly approach the last species than Lagopus albus, as the young birds of Willow-Grouse have the rusty brown colour much more developed (so that the breast can be said to be a rusty yellow with irregular black patches or broken cross bands). The under tail-coverts are barred by greyish white and brown as in Te¢rao tetrix. The throat is barred, but not so manifestly as the breast. 232 MR. R. COLLETT ON HYBRID GROUSE. [Apr. 20. The covering of the feet is still thin and incomplete, and the hair- like feathers have only appeared on the innermost toe-joint ; the claws are brown horn-colour, resembling those of the Blackgame, but their form is more like those of the Willow-Grouse. The change of the young to winter plumage (Pl. XXII. fig. 2) proceeds in about the same manner as in the Willow-Grouse; and, analogously with what takes place in them, the first plumage has not always time for development all over before it is dislodged by the winter garb. As already mentioned, the remiges with their longer coverts, the abdomen, and after them the tail-feathers, are the first parts which moult into the winter garb. In the beginning of October the young plumage of the male is half lost, and the winter plumage completed on the tail and belly, and partially on the back, whilst the head, neck, and upper breast are still mottled brown; one or two brown autumnal feathers are also long retained on the flanks. The covering of the toes is still scanty. The Christiania Museum possesses several such specimens. Sea. As previously mentioned, amongst the twenty-two known specimens from Norway there are but two females. This may partly be for the reason that the hens even in winter plumage have on the whole a less attractive plumage than the males, and therefore might be more easily overlooked, or pass for a white-speckled Greyhen. But the main cause may probably be a different one. It is a well-known fact, confirmed by a majority of instances, that amongst hybrids an unusually large percentage of males are produced. If compared with the other and better known hybrid of the Tetraonide, the “ Rakkel- fugl” (Tetrao tetriv male + Tetrao urogallus female), it will appear that there are perhaps ten males to one female. However, it must be remembered that the female Rakkelfugl is even to a greater extent more likely to be overlooked than the hen of the Rype-Orre, as it exactly resembles a small female Tetrao urogallus, so that this proportion cannot be computed with accu- racy. a all the males dissected (in winter) the ¢estes have been found to be small, although not rudimentary or abnormally formed. Their colour was greyish white; the left was generally larger than the right, and measured in one specimen 5 millim. in length, the breadth about 3 millim. In another, and this towards the spring (28th February), they were unusually small, barely 2 millim. long. In the hens, which were also shot in winter, the ovary was visible on the left side like asmall whitish patch; the eggs were hardly discernible. Supposed Parentage. Which species contributes the father and which the mother to this peculiar hybrid is as yet unknown. Only exceptionally has it fallen to the lot of an intelligent sportsman to see it in its living state, and then only for the few seconds in which it rises, to fall 1886. } MR. R. COLLETT ON HYBRID GROUSE. 233 again to his gun. The knowledge of its life and habits therefore amounts to almost nothing, and no observations have been made in Norway which can give any information concerning its origin. The existence of this hybrid arises from the fact that both parents not unfrequently inhabit the same localities. Thus Tetrao tetrix in the southern valleys of the land, where most of these liybrids are met with, regularly ascends to the elevated birch-forests on the mountains, and establishes itself in the regions where Lagopus albus has its proper home. On the other hand, but more rarely, Lagopus albus descends and breeds in the upper portions of the conifer-woods, where the other species is still to be met with in numbers. In the northern portions of the country, however, where both species live almost at the same elevation above the sea, and still more commonly share the same place of residence, the Tetrao tetrix on the whole appears in much lesser numbers than the other species, and the hybrids are here apparently more rare. It is not easy to understand the true reason for the pairing between two species so different in their habits, appearance, and nature. One of the specimens obtained in Norway was shot at a place (Saltdalen in Nordland) where no want of mates of either species could be observed in the neighbourhood. Connections of this kind are _ repugnant to nature, and in many cases the only feasible explanation is to be found in imagining a violent and irresistible desire to breed out of the species. Concerning the question of the origin, it is first of all necessary to find out whether one or two sorts of such hybrids exist—the one bred between the male Lagopus albus and female Vetrao tetriz, the other between the male Z'etrao tetriv and female Lagopus albus’. But as it is an established fact that all individuals hitherto found (with us) of the Rype-Orre, if obtained at the same season of the year, are on the whole singularly alike both in size and the colouring of their plumage, their origin cannot be ascribed to more than one of the two possible connections. When Prof. Nilsson in 1817, in his ‘ Ornithologia Suecica,’ treated of its descent for the first time, he mentions it (p. 303) as “ Hybridus a Tetrice patre et Tetr. subalpino femina”*. This assumption that it is the male of Tetrao tetriz which has formed an illegitimate connection with the female of Lagopus albus (as it is also the Blackcock that with the female of Vetrao wrogallus produces the ‘“ Rakkelfugl”), has always been and is still gene- rally accepted by most naturalists. Upon this theory it has received the names :—Tetrao lagopoides, Nilss. Skand. Fauna, 1st ed. (1828), and 7'etrao lagopides, 2nd ed. (1855); Yetrao lagopodite- tricides, Sundev. Svenska Fogl. p. 255 (186-2), (being the descendant of Tetrao tetriz, mas, it had to bear its generic name) ; and, finally, 1 A hybrid between Lagopus mutus and Tetrao tetrix is rather improbable, on account of the very different haunts of these species. 2 * Qui vero videt (illas) varietates, non diutius dubitare potest de libidine Tetricis ad furtivos amores cum congeneribus instituendos semper paratissima.’’ (Nilss. 7. c.) Proc. Zoou. Soc.—1886, No. XVI. 16 234 MR. R. COLLETT ON HYBRID GROUSE. [Apr. 20, Lagopotetrix layopoides, Malm, @fv. Kgl. Vet.-Akad. Férh. 1880, . 30. ¥ In opposition to this assumption respecting its paternity, in 1872, in a treatise “‘ Remarks onthe Ornithology of Northern Norway ’”’ (Forhandl.Vidensk. Selskabet i Christiania, 1572, p. 238), I advanced the opinion that the Rype-Orre was an offspring of the male Lagopus albus and female Tetrao tetriv, a theory which, singularly enough (although without any proof), was started by Sommerfelt so early as 1823 in his descriptions of the specimen in summer plumage’ (cf. above). Insupport of this theory I certainly could not produce direct observations or positive proofs, but I stated some circum- stances which, according to my views, caused the descent from the male Lagopus albus to be more probable than from that of the Blackeock. In conclusion, I expressed the hope that intelligent sportsmen or naturalists might soon be fortunate enough to insti- tute observations by which this question might be clearly solved. Although this was written fourteen years ago, nothing has as yet appeared in northern literature to throw a light on the subject. I shall not here set forth at length the reasons which caused me to advance this hypothesis ; they will be found given in Dresser’s ‘ History of the Birds of Europe,’ vol. vii. p. 213. They are chiefly derived from a comparison with the second and _ better-known hybrid, the “ Rakkelfugl,”’ concerning which it is an undoubted fact that it is descended from the male Yetrao tetrir and the female Tetraourogallus. In this case, too, the father belongs to the smaller, the mother to the larger species; and the offspring is a hybrid in which the male is of about. the same size as its mother. It is also a well-known fact that the male Willow Grouse is often found in the breeding-haunts of the Tetrao tetriz, and undoubtedly frequents them more often than is generally known. | Every sports- man is aware that amongst the Willow-Grouse (and the Ptarmigan) an excess of males is to be met with, which throughout the summer ramble about on the mountains, and these are probably willing to form connections whenever an opportunity offers. My friend Prof. Friis has witnessed a remarkable proof of the eagerness of the male Willow-Grouse’s desire to mate. In the spring of 1857 he observed at one of the most elevated farms in Nordmore (Bergen stift) a male Willow-Grouse which for several succeeding days kept near the house and endeavoured to form a connection with a white speckled domestic hen. Finally it is worth recording that two young male Rype-Orre, shot in October 1845, in Hedemora, Sweden, were accompanied by a female bird, apparently their mother, which was supposed to be a Greyhen*. This observation would have been of great weight in 1 “Af denne Slegts (Tetrao) hybride Yngel forekom mig paa Toten i Juli Maaneds Begyndelse folgende, som s¥gnes at vere en Affodning of Aarhénen og Rype-Hannen ” [From the hybrid brood of this genus I obtained the following in the beginning of July, which appears to be an offspring of the Greyhen and the male Willow-Grouse] (Nyt Mag. f. Natury. 1st ser. vol. ii. Christiania, 1823, p- vl): 2 (fy. Kgl. Vet.-Akad. Forh. 1847, p. 201. 1886. ] MR. R. COLLETT ON HYBRID GROUSE. 235 supporting the theory, if it had only been clearly proved, as probably the young hybrids continue to follow their mother for long. I again remark that for the theory of parentage here advanced there is indeed no positive proof, and that it is an hypothesis which may be wrong, but that it appears to me to have at least as much reason in it as the older one (which is also without proof) of the descent from the male Blackeock. On the whole it is remarkable enough that up to the present not one direct observation has been made (such as an observation of the two species in copuld in their wild state, or of the two species pairing in captivity), That such observations will not be wanting hereafter, is a matter of course. I have just received a fresh contribution to this question in a letter from Dr. Pleske, dated St. Petersburg, 16th March, 1886, in which he directs my attention to a communication from Mr. A. Rasin in ‘Journal fiir Jagd und Pferdezucht’ (‘Journal Ochoty i Konnosa- wodstwa), 1869, pp. 340-341, with the title “ Eine Siindenfall des Schneehuhnes.” From this it would appear to be proved that the Tetrao tetriz is the father, Lagopus albus the mother. This report, the original of which I cannot peruse, is referred to in the following terms by Dr. Pleske :— ‘‘Im Kreise Nowgorod, auf dem sogenannten Konewschen Moos- moraste, wurde eine Kette Hiihner gefunden, die von einem 9 des Lagopus albus, welches erlegt wurde, gefiihrt wurde. Von den zwei erbeuteten Jungen hatte beide einen vollstandigen Habitus junger Birkhiihner, waren auch grésser als die Mutter, und unterschieden sich von echten Birkhthnern nur dadurch, dass beim einen 4 Steuer- federn und zwei Schwungfedern des rechten Fliigels weiss waren, beim anderen der linke Fliigel vollstiindig wie bei Lagopus albus gezeichnet war, nicht allein in Betriff der weissen Schwungfedern, sondern auch der rostrothen Deckfedern.” If the original commu- nication gives no further information upon the subject than the words cited above, no proof is given, in my opinion, that these two specimens were really hybrids. In the first place there is no description of the covering of the toes, which is the only feature in its diagnosis that is reliable at every age and in every plumage ; and, secondly, the true Rype-Orre has never, so far as I am aware, been known to have white feathers in the wing (even the young Lagopus albus, before they assume their autumn dress, have brown wing-feathers), and it is still less likely to have them on the tail. The fact that the two young specimens were not even similarly coloured, speaks also for the probability of their being only partial albinos of 7. te¢riz, which in so many instances have been and still are taken for the Rype-Orre. It may be open to question whether, upon the whole, it is necessary to designate a hybrid by a scientific appellation, even if, like those of the ‘Tetraonide, it arises spontaneously, and, as it were, normally. The “ Rakkelfugl” has, as is known, received from Nilsson the name Tetrao urogalloides (1828) or urogallides (1835), which was altered by Sundevall to Tetrao urogallo-tetricides (186—!), and by me to Tetrao urogallo-tetrix (1872). In accordance with this, as I have 16* 236 MR. R. COLLETT ON HYBRID GROUSE. [Apr. 20, pointed out in my previously mentioned article of 1872, the “ Rype- Orre” should receive the name of Lagopus tetrici-albus, assuming that the descent is as above supposed. Other Hybrids of the Genus Lagopus. 1. Lagopus scoticus and Tetrao tetriz.—In the spring of 1877 I had the opportunity of examining a specimen in Mr. Dresser’s collection in London which was considered to be a hybrid between Tetrao tetrix and Lagopus scoticus. This specimen was a male, shot in Scotland on the 12th of September, 1876. Its hybrid nature was discernible at first glance from the formation of the tail and the covering of the toes, which were exactly like the northern ‘Rype-Orre. The colour was brownish black, the back was finely mottled with brown on an almost black ground; the breast was black, the head and throat black with fine brown spots ; the abdomen had reddish-brown cross lines, the lower tail-coverts white edges, as also had several of the feathers on the sides of the rump. In conformity with the name which above is given to the North- European Rype-Orre, the Scotch specimen, provided the mother in both instances is Tetyao tetriz, has been named Lagopus tetrici-scoticus (Nyt Magazin for Naturv., Christiania, 1877, vol. xxiii. p. 163). Another specimen of the same hybrid, also a male, was described by Malm, from Gothenburg, in Sweden. This was found in December 1877, at a spot where Lagopus scoticus had been introduced in 1861 and 1862 (Cifv. Kgl. Vetensk.-Akad. Forh. 1880, p. 17). This bird was called by Malm Lagopotetrix dicksonii. 2. Lagopus albus and Lagopus mutus.—As in the previous notes it has been supposed possible that the male Lagopus albus may be as desirous of forming an illegitimate connection as the male Tetrao tetriz, I shall touch upon another question affecting the same subject. It has probably appeared to be strange that, notwithstanding that Lagopus albus and Lagopus mutus often appear in considerable numbers in the same districts in Northern Europe, and generally share each other’s haunts, no evidence of a cross between them, so far as is known, has ever appeared. It is not probable that the cause of this should have its origin in a true repugnance in the two closely- allied species to form hybrids. Probably these hybrids are less rare than one imagines, as it requires an accustomed eye to discern them in the multitudinous garbs in which these two species appear from spring-time until the approach of winter. Even I myself have but once found one, which is now mounted in the University Museum at Christiania. It was shot at Roros in the middle of September 1883. This specimen is an old male in autumnal plumage, and is thus at a stage when the contrast between the plumage of the two parents is most marked and striking. At this time the old Lagopus mutus obtains its peculiar bluish-grey autumnal dress, in which each feather on a light ashy-grey ground is finely freckled with black, without forming distinct cross lines, whilst in Lagopus albus each feather has reddish-brown spots and cross lines on a black 1886. } MR. R. COLLETT ON HYBRID GROUSE. 237 ground. In the hybrid specimen the colour and markings of the feathers are a complete mixture of the two species. The upper plumage most resembles Lagopus mutus, as the feathers there and on the flanks are finely speckled with black, but on a somewhat reddish ground, though this is not of so strong a colour as in Lagopus albus. The pattern on the feathers is almost similar to Lagopus mutus, and the long feathers on the flanks and the upper tail-coverts, which are wanting in distinct cross lines, especially differ from the corre- sponding parts of Lagopus albus. One or two feathers, however, resemble the last species. The cross bands on the head are also much the same as in Lagopus mutus, and thus more dense than in L. albus, but rather indistinct and irregular. The lores are speckled with traces of the black colour which is peculiar to Lagopus mutus. The under-plumage is borrowed most from Lagopus albus, especially in colour. Tie feathers are transversely barred as in Lagopus mutus, but the colour is red, almost similar to that of Lagopus albus. The fine cross lines are particularly sharply defined and numerous from the bill to the vent, an unknown feature in Lagopus albus. This hybrid has, on the whole, adopted the pattern of its feathers from Zagopus mutus, and the colouring (especially underneath) from Lagopus albus. The bill in size was intermediate. It is naturally impossible to state which of the two species supplies the father and which the mother. 3. Bonasa bonasia and Lagopus albus,—Amongst the specimens belonging to the Upsala Museum sent to me for examination there was a fifth specimen which appeared to be an example of quite a new combination. It was stated by Dr. Kolthoff to have been captured in Jemtland (Sweden) in November or December 1884. The covering of the tees is just the same as that of the normal Rype-Orre. The colour is lighter than any of them, the whole upper parts, and especially the tail-coverts, having broad white (not whitish) edges. The inner hidden parts of the back-feathers are particularly dark and somewhat mixed with brown. The tail-feathers, especially at the root, are much mottled with whitish grey, and the outer feathers edged with white on their inner halves. The underside is white, with the throat biack, and with dark-coloured but not cross-lined feathers on the flanks hidden under the white. The head is unusually white, with small dark edgings on the feathers of the forehead, and greyish ear-coverts. The inner half of the under tail-coverts is blackish. Although the specimen was a male bird with well-defined ¢esées, its size was even less than a female Rype-Urre (wing 181 millim.), and was about the same size as Lagopus albus. It is therefore impossible that this specimen could have been the produce of a cross between Willow-Grouse and Blackcock, Neither is its tail forked, but somewhat rounded (the outer tail-feathers 115 millim., the centre ones 118 millim.) and contains but 16 feathers. It is therefore more reasonable to suppose this individual to be a cross between Bonasa bonasia and Lagopus albus, even if one must 238 MR. R, COLLETT ON HYBRID GROUSE. [Apr. 20, recognize the fact that these two species but seldom meet; but such is by no means an impossibility. 4. Lagopus scoticus and Lagopus mutus.—A supposed hybrid between the Red Grouse and the Ptarmigan was exhibited at the meeting of this Society, November 5, 1878, by Prof. Newton. The bird was shot in September, 1873, in Sutherland. ‘As will be seen, it bears some considerable resemblance, above, to a hen Ptar- migan in summer plumage; but its general appearance is much darker. Beneath, there is a greater resemblance to the young of the Red Grouse ; and the primaries are much as in that bird, being, however, partially edged with white to a much greater extent than is commonly found in the latter.” (Proc. Zool. Soc. 1878, p. 793.) Habits. Concerning the habits of the Rype-Orre very little is known. Almost all the specimens which hitherto have been discovered have been brought to the towns with other game snared or shot in the autumn or winter by peasants, without attracting any notice. The peasants themselves, as a rule, regard them as a peculiar kind of Willow-Grouse. In the following instances only have I heard of its being shot by true sportsmen who well knew what it was they had brought down. On the 30th of November, 1871, a male bird was shot by my friend Herr Berbom, Inspector of Forests, in Saltdalen (within the Arctic Circle), the most northern spot in which this hybrid is known. The locality was a low hill covered with birch-woods, some tarns and marshes ; it was occupied by both Blackgame and Willow- Grouse. Mr. Berbom has just informed me, in reply to my in- quiries, that this specimen appeared to be solitary, keeping company with neither one uor the other species. The other case does not either throw any particular light on its habits. On the 7th of October, 1876, another friend, Engineer Oxaal, while shooting ‘‘ Li-Rype” (Willow-Grouse) at Roros, shot one (a female) in the usual haunts of the ‘“‘ Rype,” about 2700 to 3000 feet above the sea. It was on the ground, and ran forward from behind a tuft of grass after the dog had pointed. It was therefore shot whilst running, and in this respect it appeared to Mr. Oxaal to differ from a Willow-Grouse, which at such a time would in all probability not have exposed itself. It was alone, and no Willow- Grouse or Blackgame were met with in the neighbourhood. Not- withstanding that the season was but little advanced, this bird had completely adopted its winter dress, and scarcely a feather remained of its summer plumage. An older account from Sweden gives a little more information concerning its habits. In October 1846 two young birds were shot in Dalarne which were accompanied by a hen, supposed to be their mother, and which appeared to be a female Zeérao tetriz. On this occasion one of the two young birds perched in the trees (unlike a Willow-Grouse, but like a Blackcock). They had a harsh cackling 1886.] MR. R, COLLETT ON HYBRID GROUSE. 239 ery, “ which resembled that of the Capercailzie.”” (Levin, Gfv. Kgl. Vet.-Akad. Forh. Stockholm, 1847, p. 201.) Most of the specimens which have come into my hands in a fresh state had no gun-shot wounds, and probably had been snared; but whether these were taken in snares together with Rype in districts frequented by the latter, namely in the regio alpina (the upper limits of the birch-region on the mountains), or with Zetrao urogallus and 7’. tetriz in the forest-regions, cannot be stated with any certainty. If remains of their food are examined it will probably be found that they more usually share the quarters of the Willow-Grouse than those of the other species. One of the specimens sent to the University Museum (from Sande Sogn, Nov. 9, 1881) was shot not far from the Christiania Fjord, in a district where the Lagopus albus certainly breeds, but in very few numbers, and this is hardly an annual occurrence, the locality being comparatively low. The sender of this bird, who regularly received game from that place, deemed it certain that it had been captured along with Blackgame, as it was forwarded to him in a bunch of these birds, and he never received Willow-Grouse from there. Food. In some of the individuals opened by me the food was still partially or wholly entire, and consisted of the following :— 1. Male, Dec. 7, 1870: a number of fragments of a Salix (15 millim. in length), fragments and numerous berries of Myrtillus nigra, tops of Calluna vulgaris (about 30 millim. in length), and a few leaves of Arctostaphylos alpina. 2. Male, Dec. 6, 1872: tops and seeds of Carex stellulata, a few berries of Oxycoccus palustris and Juniperus communis, some of the latter in an unripe state. 3. Male, Feb. 28, 1873: leaves of Vaccinium vitis idea, fragments and buds of a Salix and of Myrtillus nigra. 4, Female, Jan. 1875: a number of ripe and unripe berries of Juniperus, also a number of the peculiar bunchy leaves of that bush, in which Cecidomyia juniperina had formed their capsules; a large number of stalks of the Myrtillus nigra (about 12 millim. in length), some leaves of Vaccinium vitis idea, some old female and many young male catkins of Betula glutinosa (the mountain form, alpigena), and, lastly, the twigs of a haired Salix (S. glauca’). 5. Female, Oct. 7, 1876: some berries of Empetrum nigrum, also stalks of Myrtillus nigra. 6. Male, Dec. 27, 1879: leaves and berries of Oxycoccus palustris. 7. Young male, autumn, 1880: berries of Oxycoccus palustris, also the top of a Carez. From these examples it will be seen that this hybrid both in winter and summer derives nourishment from about the same sources as the Willow-Grouse, namely stalks of willows and bilberries, 240 MR. R. COLLETT ON HYBRID GROUSE. (Apr. 20, also leaves and twigs of different plants, procured principally on the marshes, and occasionally (like Arctostaphylos alpina) from the true alpine district ; likewise from various berries, and occasionally from birch-catkins. Several of these articles of nourishment form the food of Blackgame; nevertheless it is certain that most of them come from marshy places, from which it must be assumed that its diet most resembles that of the Willow-Grouse, Skeleton. In a skeleton of a male from Saltdalen (Nordland) the measure- ments are as follows :— rillim. Length of the skull (bill included) .......... 63 Greatest breadth of the skull .............. 28 Lenpth of Seapula.. a.m. aan» shay =. iS gee ee Diemer Ge OL, ENMMIEE US ona dn ne 1s > eo ce NSN UR GE PRUNES coos owen sn cna ia acne ED Length of ulna... .....2..--20 a: suena aA Length of os coracoideum .............--- 55 Length of metacarpus Il. .... Ae. Length of the two phalanges of digitus 11 Eloy ispape Se Length of furcula (to the aoe of the flee 66 Leneth of sternum..... A Ss iy 2) ae Greatest height of crista tee 34 Length of pelvis (to the first caudal ek aie << aged Greatest breadth of pelvis (across ossa ischii). . 57 DEE Ge Ce ga A ee Te eee PA eh! Length of fibia” . .. 2.5. - 2s puto AR Ae 21 Length OUGHT STS: oct fom nicl eho i total ek ta ae ener ee 45 Length of middle toe (claw not included) ...... 45 As the skeletons of the two parents, Lagopus albus and Tetrao tetriz, resemble each other so nearly that, apart from their difference cf size, it would be difficult to find out the most trifling characteristic, this hybrid hardly has one distinctive feature in the structure of its skeleton beyond its difference in size. Christiania, March 1886. EXPLANATION OF THE PLATES. Puate XXI. Hybrid between Lagopus albus and Tetrao tetriz. Fig. 1. Male in winter dress. Fig. 2. Female in winter dress. Prate XXII. Hybrid between Lagopus albus and Tetrao tetriz. Fig. 1. Young male in early autumn dress. Fig. 2. Young male in late autumn dress. durt jaPyuey “XIYLEL OVALSAL GNV sNdTv SndOdVT N4AMIAG ASNOUD CldaAH > a SWTANOUHLAYA VHENVSONALO —— . ‘dun: soug wrepatyy , wT PR MYO Md TIXX ‘Id “9861 °S N A, 1886.] MR. BOULENGER ON A NEW IGUANOID LIZARD. 241 5. Description of a new Iguanoid Lizard living in the Society’s Gardens. By G. A. Bouteneer., F.ZS8. [Received April 6, 1886.] (Plate XXIII.) Amongst the recent additions to the Society’s living collection of Reptiles is an example of Lizard of the genus Ctenosawra, which the Secretary has requested me to determine. It belongs to an undescribed species, which I propose to call CTENOSAURA ERYTHROMELAS, sp.n. (Plate XXIII.) Body a little depressed. A slight indication of a dorso-nuchal crest. Scales on posterior part of back a little larger than ventrals, rhomboidal, indistinctly keeled. Upper surface of hind limbs with large spinose scales. ‘Tail shorter than head and body, much de- pressed, except quite at the end; its upper surface with transverse series of very large, subequal spines, directed wpwards and back- wards, alternating with series of very small scales; the series of small scales inconspicuous, at first glance, on the anterior half of the tail» lower surface of tail with smaller pointed keeled scales, the number of transverse series being the same as on the upper surface. ight femoral pores on each side. Blackish olive above, with a large patch of vermilion-red on each side of the body, and variegations of the same colour on the sides of the head and neck ; lower surfaces grey, throat marbled with red; three oblique black bands on each side behind the fore limb; two black bands across the humerus. Tympanum yellowish. Iris golden. Length from snout to vent 100 millim., head 24, tail 88. The locality of the single specimen, acquired by purchase of Mr. W. Cross of Liverpool on the 3rd inst., is not known. This new species again lessens the gap between the genera Cteno- saura and Cachryx. I therefore propose to unite the two genera. In connection with this subject I must draw attention to an extra- ordinary statement to be found in one of Prof. Cope’s latest papers’. He remarks :—“ This genus (Cachryz, Cope) is of the type of Cteno- saura, differing only in the characters of its tail. It lacks the ter- minal portion, which is in that and other genera free from spinous seales. It is not in my opinion allied to Urocentron or Hoplocercus, as suggested by Bocourt, genera which belong to the terrestrial division of the family, or Humivage.”’ Mr. Cope not only omits to add that I was the first to assign his genus to the correct place in the system, but forgets that he is himself responsible for the error now corrected, and not M. Bocourt, who simply endorsed his views; for on referring to Cope’s original (and unique) account of Cachryx* we read, ‘This genus is allied to Urocentrum and Hoplurus, ut differs in the possession of femoral pores.” 1 Proc. Amer. Philos. Soc. 1885 (1886), p. 270. 2 Proc. Acad. Philad. 1866, p. 124. 242 MR. G. A. BOULENGER ON RANA ARVALIS. __[Apr. 20, 6. Remarks on Specimens of Rana arvalis exhibited in the Society’s Menagerie. By G. A. Boutenesr, F.Z.S. [Received April 14, 1886.] (Plate XXIV.) An interesting addition has recently been made to the series of Batrachians in the Society’s menagerie—the Oxyrrhine Frog, Rana arvalis, Nilsson, so often described and its specific validity discussed. It is, with the exception of Rana iberica, Blgr., the only European Batrachian as yet never figured. The accompanying illustration (Plate XXIV.) is intended to supply this desideratum. My friend Professor Born, of Breslau, favoured me this spring with about 50 breeding specimens of the Frog in question, some of which have been presented to the Society. Two years ago, I also received a number of these Frogs from the same gentleman, which have afforded me an opportunity of verifying the additional observations on the characters of the species recently made by Pfliiger and Smith’. These authors have shown that some of the characters hitherto regarded as diagnostic comparatively to R. tem- poraria are not constant. Thus the shape of the snout, often given as the principal distinctive character of the two species, is not absolutely constant ; and specimens of &. arvalis may be found with the snout less pointed than certain specimens of R. temporaria. Also breeding males of the former species possess black rugosities on the thumb in every respect similar to those of A. temporaria. This statement I have been able to verify not only on the Breslau specimens, but on a Swedish one, for which I am indebted to Dr. Westerlund. However, the breeding specimens from Copenhagen, in M. Lataste’s collection, which I described in my monograph of the Rane temporaria, have grey, not black, asperities. It is therefore a question whether the colour of the copulatory asperities does not vary according to localities. Besides, the web between the toes is longer in the Copenhagen specimens. The character derived from the vomerine dentition has also been shown by these authors to be an unreliable one. I may add that the remark is not only true in this case, but applies to European species of Rana generally ; among the hundreds of specimens of Rana esculenta which have been examined by me, not a few have the vomerine teeth inserted behind the line of the choane, and would as regards this character fall in the section 2. temporarie! Differences in the dentition exist which may often assist in the discrimination of species, but are not sufficiently constant to be regarded as good characters. The criterion for the easy distinction of R. arvalis from R. temporaria is the metatarsal tubercle ; this character is an infallible one, and will remove any hesitation in the determination. Of greater importance still, but less easily ascertainable, is the character of the spermatozoa. Should any one still entertain doubts as to the specific validity of 1 Arch. f. ges. Physiol. xxxii. 1883, p. 525. a de! a oe af a 1886.] MR. R.COLLETT ON BALZNOPTERA BOREALIs.. 243 R. arvalis, let him read Pfliiger’s account of experiments on the crossing of the German frogs. Dissidents from the modern views on the specific distinctions of the forms of /. temporaria have of late become very few. That there should be at the present day a naturalist to express the opinion that R. arvalis is the male and R. temporaria the female of the same species, and a herpetologist, who professes to know European Frogs, to reproduce such nonsense with the remark “ should this discovery be confirmed it will afford an uneapected solution to the controversy,” may appear incredible, but is unfortunately true. APPENDIX. The following paper, originally intended for the ‘Transactions,’ has been ordered by the Committee of Publications (at the request of the Author) to be printed in this part of the * Proceedings ’:— On the External Characters of Rudolphi’s Rorqual. (Baleno- ptera borealis). By Rosurr Coxiert, C.M.Z.S.* [Received January 4, 1886: read February 2, 1886.] (Plates XXV., XXVI.) Contents. I. Introductory Remarks, p. 243. X. Parasites, p. 255. If. General Characters, p. 246. XI. Time of capture, p. 259. III. Measurements, p. 248. XII. Fetus, p. 260. IV. Structure of the Body, p. 248. XIII. Food, p. 261. V. Colour, p. 249. XIV. Habits, p. 263, VI. Flippers and other external XV. Value, p. 263. characters, p. 252. XVI. Monstrosities, p. 264. VII. Baleen, p. 253. XVII. Synopsis of the four northern VIII. Blow-holes and furrows, p.255. species of Balenoptera, IX. Hairy covering, p. 255. p. 264. I. Introductory Remarks. Although our knowledge of Balenoptera borealis has been con- siderably increased during the last few years, still almost all researches have been confined to its anatomical structure, and no complete description has hitherto been given of its external characters. Even up to the year 1882 the species was only known from a small number of stranded specimens, the skeletons of which had found their way into different museums ; but of the external characters of * (Mr. A. Heneage Cocks, F.Z.S., has kindly added some footnotes, which are designated by his initials. —Ep. | 244 MR. R. COLLETT ON BALZNOPTERA BOREALIS. [Feb. 2, these examples either no particulars were obtained, or at most a few scanty remarks by casual observers *. In 1882 a whaling-factory was established at Sodrver near Hammerfest (West Finmark) for the purpose of catching the Blue- Whale (B. sibbaldi), wnder the management of Capt. Bull. It was soon seen that the greater number of the whales caught here were the so-called ‘‘ Sejhval,” a species with which Capt. Bull was acquainted through his former whaling-expeditions in the Varanger- fjord, but in this Fjord, as well as along the whole of the East Finmarken coast, it had only appeared casually. Eight specimens of this “ Sejhval”? were caught at Sdrveer the first year, 1882, and in the ensuing years it was also taken, though in varying numbers. In 1883 40 specimens * were caught, in 1884 only 3, this year (1885) 44. By gradually collecting together the scattered accounts respect- ing this whale it soon became evident that it was a species distinct from the three other Balenoptere ; and both Prof. Sars and I soon came to the conclusion that it might be ‘‘ B. laticeps,’ Gray=B. borealis, Lesson, or the same species to which the skeletons just referred to belonged, two or three of which (among the few hitherto known) had been brought from precisely the same region. Last year (1884) Dr. Guldberg, in a paper published in Bull. Acad. Roy. de Belg.’, finally proved by the researches he had been able to make, at Sdrver, upon some parts of the skeleton (now 1 These specimens are as follows :— 1811. One stranded in the Zuyder-Zee, Aug. 1811 (Hschricht, Kgl. D. Vid. Selsk. Skr.5 R.1B.). Length 382’, The skeleton is preserved in the Leyden Museum. 1819. One stranded on the coast of Holstein in Feb. 1819, and described by Rudolphi as B. rostrata (Abh. konig]. Acad. Wiss. Berl. 1820-21, p. 27). Length 323’. The skeleton is preserved in the Berlin Museum. 1861. A skeleton sent to the museum at Brussels from East Finmarken (Norway) through Eschricht (V. Beneden et Gervais, Ostéographie des Cét. viy. et foss. p. 201). Length 32’. 1861. One stranded, June 1861, in Altenfjord, West Finmarken (Norway). Length of the skeleton 30' 1" (Swed.) [about 29 feet 34 in, English.— A. H.C.]. Described by Lilljeborg (Ups. Univ. Aarsskr. 1862, p. 25, Sver. och Norg. Ryggr.-djiir, B. ii. p. 943, 1874). The skeleton is in the Bergen Museum. 1863. One stranded in Skogsvaag, near Bergen (Norway), July 1863. The skeleton not preserved. (Dr. Koren in a letter to Prof. Lilljeborg, dated Bergen, Jan. 24, 1864.) 1872. One caught in the Firth of Forth, September 1872, described by Turner (Journ. Anat. Phys. April 1882, p. 471). Length 38’ (English). The skeleton is in the Anatomical Museum at Edinburgh. 1874. One stranded in July 1874, at Biarritz (Basses Pyrénées). Length 7830 mm. (25' Rhen.), and described by Fischer (Compt. Rend. 1876, tom. 83, p. 1298, &e.). The skeleton is in the Bayonne Museum, 1883. One caught on the coast of Essex, England ; described by Flower (Proc. Zool. Soe. Lond. 1883, p. 513). Length about 29' (Engl.). Skeleton prepared for the Sydney Museum. 1884. One taken at Goole, Lincolnshire. Skeleton in British Museum. ? [I fancy there is some mistake about this number, and that 15 was the total of this species taken by Capt. Bull in 1883, and that 40 was his total take of all species during that season. —A. H. C.] 1886.] MR. R. COLLETT ON BALEZNOPTERA BOREALIS. 245 preserved in the University Museum at Christiania), and a foetus from the same locality, that the Finmark “ Sejhval ’’ is identical with B. borealis. Thus, whilst B. borealis, as has been stated, is a constant summer visitor on the coasts of West Finmark, where it has annually, although in varying numbers, occurred off Soréen, near Hammerfest, probably to gorge upon the ‘Aate,” or the shoals of Crustacea which constitute its food, it has, as mentioned above, only exceptionally visited East Finmark, and on the coast east of the North Cape only a few specimens had been caught, and not every year. It does not, however, appear to have been altogether unknown even on this part of the coast. During a stay in Finmark in 1878 I received information that a shoal of 13 whales, of about 40 feet in length, had stranded in a bay of the Porsangerfjord to the east of the North Cape. I did not have an opportunity of visiting the place ; but as the baleen-plates of these Whales were described as being black, it seems very probable that they belonged to this species”. In the same month 5 similar small whales were stranded at Sorveer, near Hammerfest (where the above-mentioned factory had not then been established). Moreover, several whalers have informed me that this species visited the Varangerfjord-in 1879 and 1880, but was not caught; they also noticed that whenever this species came in, B. sibbaldi left the coast and went out to sea®*. During the past summer, 1885, the Sejhval (B. borealis) came quite unexpectediy under land along the whole coast of Finmark, not singly or solitarily, but in such large numbers that, during the whole summer, most of the whales caught both in West and East Fin- mark consisted of this species. Of the other species, B. sibbaldi, B. musculus, and Megaptera boops, which in former years had formed the majority, only a comparatively small number were caught’. Of B. borealis 724 specimens were caught by 18 companies stationed in Finmark, and 47 specimens by 3 companies, ou the Murman coast, making together a total of 771 specimens. In fact they were caught by all the companies along the whole 1 “Sur lexistence d’une 4me espece du genre Balenoptera dans les mers septentrionales de l’Europe” (Bull. Acad. Roy. Belg. 3° sér. tome vii. no. 4, Ayril 1884). This paper is translated (with a few additions) in Journ. of Anat. and Phys. 1885, p. 293. 2 Nyt Mag. f. Naturv. 27 B. p. 260 (1885). ® Tt was therefore said this year in Finmark that as B. borealis was under land, B. sibbaldi would not come, and this presumption proved to a great extent correct. 2B. sibbaldi was this year almost absent from the Norwegian coast as compared with the preceding years; but it was more common further east, as 5 whalers on the Murman coast killed almost exactly the same number of that species as all the 31 Norwegian whalers did together. * [Of Megaptera boops rather more examples were caught than in any previous year; this does not necessarily show that they were more numerous than in other years, but, in the absence of the two larger species, they were hunted in preference to B. horealis, as yielding three times the quantity of oil.— A. H. C.] 246 MR. R. COLLETT ON BAL NOPTERA BOREALIS. [ Feb. 2, coast from Sérden, near Hammerfest, to Jarfjord in Syd Varanger, and on the Murman coast at least to Kildin. When, during a stay in the Varangerfjord in the month of July, I ascertained that specimens of B. dorealis were daily brought into the factories at Vardé, I at once proceeded to that place, and in the course of a couple of days I had an opportunity of examining the external characters of six specimens, three males and three females, whilst I saw double that number towed in, but want of time prevented my examining them. Two drawings of this species have previously been produced. According to Van Beneden and Gervais (Ostéogr. des Cét. p. 201) the first known specimen of this whale (Zuyder-Zee, 1811) was figured, but these authors are unable to explain the fate of this figure, which never seems to have been published. Another figure was given of Rudolphi’s specimen (Holstein, 1819) in a lithograph published in Hamburg, 1819; this figure is copied in Brandt and Ratzeburg’s ‘ Medicinische Zoologie’ (B. 1. tab. xv. fig. 3); it is, however, very imperfect and confusing '. As our knowledge of this species is thus still very meagre, I have thought it right to give the principal results of my researches at the factories at Vardé and Mehayn this year, although I am well aware that my observations, based as they are upon only two days’ studies on the spot, are very incomplete. I am also indebted to Messrs. Castberg, Bull, Bruun, Bryde, Ellevsen, and Sérensen, all managers of the different factories, for communications chiefly relating to their life-history as observed during their “ fishing’’ this year *. II. General Characters. Compared with the three other northern Rorquals, B. borealis belongs to the smaller group, its length being somewhere between that of B. rostrata and B. musculus, or about 44 feet. Its body is less robust than B. rostrata, more like B. sibbaldi, and much better proportioned than B. musculus. The colour on the upper part of the body is dark grey-blue, something like B. sibbaldi. The belly is more or less white as far as the genitalia, but the remainder of the undersurface and also the flippers are of the same colour as the back. The flippers are small, smaller relatively than in the other species; the dorsal fin is large, curved, and situated far forward. The baleen-plates are black; the bristles are white and much curled, and comparatively long. In the sea the B. borealis may be recognized at the first glance by its large, high, dorsal fin, which most nearly resembles that of B. rostrata, also by its head being more slender, and its snout more rounded than are those of the other Arctic species. 1 The colour is especially wrong, which is easily explained, as the animal was probably drawn a long time after death. 2 T have to offer my best thanks to my friend Mr. Alfred Heneage Cocks for the kind assistance he has rendered me by looking over the paper before it was printed. 1886.] | MUU GPPEL pees snap Jo «oqournrgy “ut OTT eects Sosa Be ae coat - aynB youa Jo yypLoag, “wut OZ8T Soe “CLE ERT wage sai ‘sete TE Jo OTN, YOUG lige, Ltsaows “Mt OT, “ULUL ()Y8 seeeee specs stereeeeeeee Tvy JO 4oOd OY} YL qy Sey (Cor nae! te Pease Garg me. sare > oasnie (‘wut [1FT) ag sacsee *[ve] JO aTppitu eq] 4B Apoq Jo qqseyyT (cum Q96L) 79 (‘wut e0gT) ee (urea $71) FG (mum $11) FG | (wut FZyT) ‘fg Ug [estop Jo e8eq wo. 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(ur tp) AGT seeeee ty wt ewer essence eerecneces soddiyg 0} noug (ru £6) 1 (ui $6) 08 (Cut 6) 6% (Wt OT) Ze ae (‘ur $8) 8g | UR Tesxop 07 yuoug (uw $cT) oF (ut TPL) AGF (FT) FF (ut Epq) 26) © Cor Bet) er | (Co ESL) eh [°° sereeees BUST [BIOT, me) “Pp “Pp . 4 . RS . ro ‘Q°ON ‘GON ‘? ON '§ ON G ON ao “SPUIUWIANSDA JT 248 MR. R. COLLETT ON BALENOPTERA BOREALIS. _[Feb. 2, Ill. Measurements. Most of the examples caught were between 40 and 50 feet in length. The usual length was 44-45 feet or thereabouts. The largest specimens measured 52 feet’ (16°3 metres). The 6 specimens which I examined thoroughly were 43 to 493 feet in length (see p- 247). ‘The last of these (a male) was considered to be one of the largest caught ; so that it may be laid down as a rule that they rarely exceed 50 feet (15°6 metres). The smallest specimens this summer that I know of were 35-37 feet, but these were exceptional. A single specimen was caught in July at Mehavn (by Foyn), the length of which was said at the place to be 323 feet (10°1 metres). Both sexes seem to attain about the same size; the largest female specimen that I examined was 47 feet long (14:7 metres). One of the managers stated that if there were any difference, the female was the largest and fattest, at any rate during the whaling- season. The size appeared the same throughout the season, and it was remarkable to notice how uniform it was, and how evidently the whales were all of about the same age. IV. Structure of the Body. The Structure of the body seems to correspond with that of B. sib- baldi, which it on the whole resembles in its mode of living. The body is highest across the middle of the flippers, where, in the case of the living animal, the height is to the total length about as 1 to 53 (as in the case of B. sibbaldi). In the stranded animal, when the belly is compressed by the ground, the proportion is as about 1 to 6. The height of the body is thus not so great as in B. rostrata, which is at that point relatively the largest of all the four species. The form of the hinder part of the body does not differ essentially from that of the other species. Immediately under the dorsal fin the height is one eighth of the total length, and halfway between the dorsal fin and the root of the tail one tenth. From these proportions it will be seen that in this respect it also correspouds most nearly with B. sibbaldi, and is neither of the exceedingly slender ‘‘ emaciated ” form of B. musculus, nor of the comparatively stout form of B. rostrata. The breadth of the body can only be given approximately, and would seem across the flippers to be not very different from the height. From the vent to the root of the tail the body is strongly compressed, and the caudal part forms, as in the other species of Balenoptera, a thin ridge above and below, which is particularly sharp along the dorsal line. The breadth at the root of the tail at ? [About 54 feet English, and so with the other measurements; the Norwegian foot almost = 123 inches English.—A. H. C.] 1886.] MR. R. COLLETT ON BALHZNOPTERA BOREALIS. 249 the narrowest point (just where the flukes commence) was in the Jargest specimen 390 mm., or about 15 inches. V. Colour. The colour of the back is bluish black or occasionally some- what brown, much resembling the colour in B. sibbaldi, although the blue colour asa rule is less pronounced than in that species. The colour after death is darker than in the living animal. On the side of the body the colour becomes somewhat lighter; the belly is dark steel-grey with a white area running along the centre; the white colour begins at the symphysis of the lower jaw, and termi- nates at the genitalia, but occasionally it is interrupted or imper- ceptible on the middle portion of the belly. Considerable variations occur in the breadth, size, and form of this white part of the belly. The throat is always white, occasionally throughout its entire breadth. scmetimes only for a couple of feet. On the breast the white becomes narrower, and in many indi- viduals is completely cut off by the bluish-grey colour of the sides, but it then reappears on the belly, and continues in a somewhat irregular width to the genitalia. Behind the vent the whole under- side of the tail is light bluish grey, about the same as the back. The white colour is not always symmetrical, but is occasionally broader on one side of the middle line than on the other; also the extent of it on the belly may be rather irregular. On the throat similarly the white colour is sometimes broader on one side than on the other. ; The white patch on the belly was never absent in any of the specimens examined; and this observation is confirmed by all the managers of the whaling companies, who state that it is always to be found, though it is sometimes only slightly developed. The white colour, especially on the throat, is pure and sharply defined. On the belly and in front of the genitalia there are, on the contrary, a large number of very fine bluish-grey lines, which are quite short and run parallel to each other; these lines, which can only be distinguished when you are near to the animal, some- times, when they are very numerous and closely set, detract from the whiteness of these portions. The flippers are coloured on the outer side like the back ; on the inner side they are a trifle lighter, especially along the lower edge: a few individuals (such as No. 2 of the specimens examined) have large whitish spots on the inner side ; these are never, however, absolutely white. The flukes of the tail are also bluish grey underneath ; the dorsal fin is exactly the colour of the back. Distributed over the dark parts of all the specimens examined were a greater or less number of whitish oblong spots of peculiar form and colour, their length being about 100 mm., and breadth about 30 (Plate XXVI. fig. 2). Their outer edges are not always sharply defined ; their colour is in general whitish grey, occasionally almost white, and more rarely dark grey. Along the centre of the Proc. Zoo. Soc.—1886, No. XVII. i7 250 MR. R. COLLETT ON BALZNOPTERA BOREALIS. _ [ Feb. 2 long axis there runs a dark line, from which to both sides and both ends run fine radii of similar lines '. These patches are most frequent on the sides of the body some- what below the middle, and occur also on the tail, but may be found, when they occur to any great extent, distributed singly right up the centre of the back, and extending as far as the end of the lower jaw. They occur on all examples, although they may not be equally apparent in all. They evidently are due to a peculiar matter in the skin, as they become more perceptible after the animal has dried for a time. Single small white spots of a normal form occur less frequently in the black portion of the sides, especially up to- wards the back. Among the markings of less constant occurrence may be noticed :—-On one of the specimens examined there was a slightly lighter patch behind the ear-opening, which began just at its pos- terior margin, and extended backwards in a pyramidal form for about a foot. In order to show the variations of the white colour on the belly, I shall briefly explain its extent in the individuals examined by myself. No. 1. A female.—Throat entirely white ; on the breast the white area became narrower, though without being completely broken off. A larger white patch “occurred at the end of the furrows, forming here an extension of the central stripe. On the belly the white colour was partly covered over by the fine light bluish-grey lines, which terminated as single white stains at the mamme. No. 2. dA female.—The white area symmetrical and ample; throat white, about ten furrows on each side being included, though the upper ones were spotted with black. The patch became narrower backwards, so that between the flippers only three furrows on each side were included, while behind the flippers it spread out in an anchor-like form, the arms of which extended rather high up on the sides (and to about half a flipper’s length from the end of the flipper). Behind the furrows the white area was almost interrupted by the grey colour of the sides, but widened out again in front of the mammee, where it was whitish and not sharply defined. The fine bluish-grey lines were most frequent towards the dark portions of the sides. In this specimen the oblong whitish marks on the sides were com- paratively few and indistinct, “although some of them were perfectly white. No.3. 4d female.—Throat white, the white commencing just behind the symphysis of the jaw, and including the eight furrows on each side of the central line; this white portion cvacished as it passed backwards. Almost exactly under the distal end of the flipper, when lying parallel to the body, it was broken off by the colour of the sides} but it recommenced at the navel, and thence extended unbroken to the mamme. ? The general form and design reminds one of the septa ina Fungia or Herpetolithus. 1386.] MR. R, COLLETT ON BALHNOPTERA BOREALIS. 251 The oblong whitish marks occurred all over the animal, from the beginning of the flippers to the root of the tail, but did not, generally speaking, extend much higher than the middle of the sides ; several small spots, however, of normal form occurred up towards the back. In this specimen the underside of the flippers had large whitish spots. at 4. A male.—Unusually dark. The white colour was com- paratively little extended, as in front it embraced only four furrows on each side, and even here was mixed with black. Backwards the white colour widened somewhat, so that six furrows on either side were included, though with black stripes from the sides extending obliquely into them. Behind the furrows the central patch was ter- minated by the colour of the sides, and there was but little white in the portion in front of the genitalia. In this specimen were noticed a large number of the peculiar oblong marks, some quite white, most of them, however, darker in hue, spread over all the dark parts of the belly, extending both downwards to the white stripe and upwards on to the back. They were most numerous about the middle of the sides and on the posterior portion of the body. No. 5. A male.—Throat white, extending over eight furrows on each side, from the front to between the ends of the flippers. Above these, six furrows on each side were mottled with white. Further back the white part was interrupted, so that the belly behind the furrows was, for a short distance, of a uniform blue-grey tint like the sides, but again became whitish, sprinkled over with the narrow bluish lines as far as the genitalia. The oblong whitish marks were present, especially on the sides. No. 6. 4 male.—Colour almost similar to that of No. 2, the white having almost exactly the same extent. Here also the white patch be- tween the flippers extended in a somewhat irregular anchor-like form. Behind the furrows the white was almost terminated by the bluish- grey colour of the sides; it recommenced at the navel and extended to the genitalia, but was pencilled over evenly by fine short grey lineolee. The oblong whitish marks were numerous, tolerably light- coloured, but none quite white, and extended almost to the end of the lower jaw. In a 7th specimen, which lay secured in the water with the belly exposed, the white colour was more decidedly asymmetrical than in any of the others. On the breast the white included six furrows on the right side, whilst the whole of its left side was black ’. The white area extended as usual to behind the end of the flippers, where it became narrow or disappeared, but extended again back- wards to the genitals, and at this point it was symmetrical on the two sides. ' A similar asymmetry of colour (left side dark, right side white) has been noted on two occasions by Professor Sars as pervading the lower jaws in B. mus- culus (Forh. Vid.-Selsk. Christiania, 1878, no. 15, p. 9; 1880, no. 12, p.3), [A imi pinke was recorded by me in the ‘ Zoologist,’ April 1885, p. 138.— iz 252 MR. R. COLLETT ON BALH/NOPTERA BOREALIS. — [Feb. 2, VI. Flippers and other External Characters. The Flippers are relatively shorter than in any of the other species, somewhat slender and pointed. Their length, measured from the axilla, is about one eleventh of the total length, occasionally a little over and sometimes under this measurement. In form they do not differ materially from those of the other species. A little beyond the middle they present on the ulnar side a slight extension, an indication of the commencement of the manus. At this point the flippers have their greatest breadth, which is, compared to their length (reckoned to the axilla), as 1 to 3°5 or 3-6 (or to caput humeri as 1 to 4°7). Thus in its small flippers B. borealis differs essentially from B. stb- baldi, which it otherwise resembles in so many points, and approaches nearer to B. musculus. Their colour, as previously mentioned, is essentially the same on the outer and inner sides, and in this respect they differ from all the other species, in which the inner side is more or less white. The Dorsal Fin is situated far forward and is high. The front margin is convex, with a slightly curved apex ; its hinder margin is deeply concave. In form and position it is quite unlike that of B. sibbaldi and B. musculus, and is most like that of B. rostrata, but it lies further forward than in any of them. The following are the proportions between the total length of the body and the distance from the end of the snout to the beginning of the dorsal fin in five of the specimens examined by me :— No. 1.. As 1 to 0°65. No. 3.. As 1 to 0°68. No. 4.. As 1 to 0°65. No. 5 . As 1 to 0°65. No. 6.. As 1 to 061. The dorsal fin is thus constantly placed anterior to the com- mencement of the last third of the body, whilst that of B. rostrata (according to Sars) is placed at the beginning of this third; it is even further back in B. musculus, and furthest back in B. sibbaldi. Its height and size is on the whole considerable, especially in comparison with the length of the flippers. The height is in fact more than 13 times the greatest breadth of the flippers, and is to their length as 1 to barely 24. The dorsal fin is possibly higher in the male than in the female, although the difference cannot be great. The length of the anterior margin is about the same as that of the base. The Flukes, in a couple of specimens examined by me, were, com- pared to the total length of the body, as 1 to 4:2. Thus they were relatively somewhat smaller than in B. rostrata (3°4), but larger than in B. musculus (4°1-5:1). Their colour is, as in B. sibbaldi, about the same on the upper and lower sides. The Anus is situated directly under the apex and posterior margin 1886.] MR. R. COLLETT ON BALEZNOPTERA BOREALIS. 253 of the dorsal fin. The genital opening lies almost immediately in front of the anterior edge. The Inferior Maxilla.—Yhe length of the lower jaw-bones (mea- sured to the angle of the mouth in the non-skeletonized animal) is, compared to the total length, as 1 to 43, viz :— ; INOsp2eekeae No. 3.. 4:5. No. 5..4°7, No. 6..4°4. In this last specimen the lower jaw-bones, probably on account of their weight, were displaced, which is often the case. ‘The jaws have the same relative length as B. sibbaldi, and are longer than in the other two species. In these three species the proportions (according to Sars) are as follows :— B. sibbaldi, 4-5. B. musculus, 5:0. B. rostrata, 5°5. ) Their greatest breadth (measured between the eyes) is, compared to their length, as 1 to 1°7. ‘This was somewhat less ina skeleton in the Bergen Museum (total length 307; feet), where the breadth across the temporal bones (according to Lilljeborg) was, compared to the length of the skull, as 1 to 2°0. VII. Baleen. The colour of the baleen is usually black and the bristles white ; in some individuals, however, a small number of the foremost rows were white, or mottled with white, but not symmetrically in each ramus. Besides the baleen in the six specially examined specimens, I examined a considerable quantity of whalebone which lay heaped up on the beach at the different establishments. Amongst all this, I only found two specimens which differed from the others in having some white mottled plates; in all the others it was entirely black. Of these two individuals, one had on the right side 58, and on the left 53 of the foremost baleen-plates mottled ', The second specimen had on the right side 52 white plates, on the left only 5°. The number of the plates was about 330 in each jaw, in some ? Namely in the following manner :—On the right side the foremost 27 were white in their outer half, and the next 15 quite white, after which came 3 grey plates. Then came 10 completely black, and finally 3 which were white with black edges. Total 58. The remainder were black. On the left side the colouring was somewhat similar. The first 31 were semi-white, and the next 9 quite white, then followed 3 blackish grey, after which came 3 white, then 2 greyish black, and finally 5 white. Total 53. The rest were black. * In this specimen on the left side the 5 foremost ones were white, all the others black ; on the right side the first 86 plates were mottled with white, after which came 16 quite white, the remainder being black. 254 MR. R. COLLETT ON BALZ NOPTERA BOREALIS. — [Feb. 2, individuals 320, in others as many as 340. No. 2 for instance had on its right side only 318, on its left 328.. The number appears to be rarely the same in the two jaws of the same individual. The front .plates were smal!, almost rudimentary, and formed double rows; these were difficult to count. The greatest length was attained at the commencement of the latter third of the series, where as a rule they measured 550 to 600 millim.’ From these measurements it appears that the length and number of the plates are not constantly greater in the right than in the left jaw, also that there is no constant difference between the plates in the two sexes. The hair-like bristles in which each plate terminates, and which form the most effective part of the straining-apparatus, are in this species unusually fine, somewhat resembling silky wool, and white * I give here the measurements of the baleen-plates of 4 examples, viz. those, of specimens Nos. 1, 3, and 5, and those of a fourth individual, the jaw of which lay on the beach. They are reckoned fr om behind forwards, so that No. 50 lies near the angle of the mouth, No. 250 nearest the symphysis of the jaw. They are measured from their base (in the freshly killed specimen) to the outermost point where the plates terminate and the bristles commence. No. 1. Female. Left all black; on the right side, the first slightly lighter colour. Left side 328 plates. Right side 324 plates. millim. millim. Hensthof no: D0. sc2cc.ss-shaped incision ; the external border is much less rufous and the pale markings upon it are paler and of twice the width; the secondaries are almost white instead of pale.grey-brown ; the series of silver spots on the under surface of the secondaries is wanting. Expanse of wings 29 millim. Murree, 8th August, 1885. This species in coloration more nearly resembles C. corylata than either of the two others of the same group. 172. CipARIA JAMEZA? Cidaria jameza, Butler, Aun. & Mag. Nat. Hist. ser. 5, vol. i. p- 452 (1878); Ill. Typ. Lep. Het. iii. p. 58, pl. lv. fig. 9 (1879). Murree, 20th August, 1885. The single worn specimen in the collection is rather larger than Japanese examples, but I can discover no other difference. 1 The collection contains a Lupithecia, but it is too much worn for identi- fication. Proc. Zoou. Soc.—1886, No. XXVI. 26 394 ON LEPIDOPTERA FROM WESTERN INDIA. [June 29, 173. CrpARIA ALBIGIRATA ¢ Cidaria albigirata, Kollar in Hiigel’s Kaschm. iv. 2, p. 489 (1848). Murree, 12th August, 1885. This agrees tolerably closely with Kollar’s description, but his statement that it belongs to the neighbourhood of Cidaria prunata and suffumata is misleading, if this be his species, since it is closely allied to the European C. picata, and decidedly more closely than to either of the above-mentioned insects; it occurs also in Afghan- istan. 174. PHIBALAPTERYX, sp. n. ? A single specimen, much faded, worn, and without any antennee or palpi, apparently of a new species. Bugnoter, 19th September, 1885. CRAMBID&. 175. JARTHEZA CHRYSOGRAPHELLA. Chilo chrysographellus, Kollar in Hiigel’s Kaschm. iv. p. 494 (1848). Campbellpore, 30th July, 1885. 176. APURIMA XANTHOGASTRELLA. Apurima wanthogastrella, Walker, Cat. Lep. Het. xxvil. p. 194. n. 1 (1863). Campbellpore, 28th July, 1885. TORTRICIDE. 177. CERACE TETRAONIS, sp. 0. Primaries above black, regularly dotted with pale yellow; costal border crossed by numerous short yellow striz ; a longitudinal sub- costal bright red stripe from base to outer margin: secondaries with the discoidal cell and costal area nearly to apex bright orange ochre- ous, remainder of the wing black; five black costal spots; an ochreous apical spot ; abdominal third of wing spotted all over with ochreous: body blackish, head and collar spotted with yellow, abdomen with ochreous margins to the segments: primaries below without yellow dotting, the red stripe replaced by an ochreous patch fillmg the discoidal cell and a spot on outer margin; the yellow colouring on the secondaries paler than above, otherwise similar ; body below whitish. Expanse of wings 28 millim. Murree, 28th August, 1885. Allied to C. onustana of Nepal. CHOREUTIDE. 178. TEGNA HYBLZELLA. Tegna hybleella, Walker, Cat. Lep. Het., Suppl. v. p. 1810 (1866). Campbellpore, 20th July, 1885. a P.Z.S *l@66s,E) Ay Maud Horman-Fisher del etlith Mintern Bros . amp} NEW LEPIDOPTERA FROM WESTERN INDIA. 1886. ] ON BIRDS FROM TARAPACA, NORTHERN CHILI. - 395 EXPLANATION OF PLATE XXXV. Fig. 1, Azanus uranus, p. 366. . Tarucus extricatus, p. 366. Spindasis hypargyros, p. 369. Euchloé lucilla, p. 376. . Pyralis incongrua, p. 383. . Samea yerburii, p. 383. . Mustilia columbaris, p. 387. . Argyria cinerea, p. 387. . Epifidonia signata, p. 3‘)2. 10. Abraxas fuscescens, p. 392. virginalis, p. 392. COD “IS: crip OY dO 9. List of a Collection of Birds from the Province of Tara- pac, Northern Chili. By P. L. Scuarer, M.A., Ph.D., F.R.S., Secretary to the Society. [Received June 25, 1886.] (Plate XXXVI.) Mr. H. Berkeley James, F.Z.S., has placed in my hands for determination a collection of bird-skins made for him by Carlos Rahmer, of the National Museum, Santiago, in the province of Tara- paca, formerly in Peru, but now, I believe, annexed to Chili. The collection, which was made in January and February last, contains 150 skins referable to 53 species, amongst which a new Flamingo, as I shall presently point out, is of special interest. The nearest. fauna to Terapacd that has received much attention is that of the Desert of Atacama just to the south, which was explored in 1853-4 by Dr. R. A. Philippi, of Santiago’. Prof. Philippi’s list of birds contains 33 species, only 11 or 12 of which are identical with those in the present collection. But our leading authority on the Birds of Peru, of which Republic the district of Tarapaca until lately formed part, is Taczanowski’s ‘Ornithologie du Pérou.’ I have, therefore, referred throughout to this most useful work except in the case of the following seven species, which are not included by Taczanowski, and are therefore additions to his avifauna, namely :—ASycalis aureiventris, Upucer- thia ruficauda, Synallaxis modesta, Bolborhynchus orbignesius, Pheeni- copterus jamest, Fulica leucoptera, and Atgialitis occidentalis, Of these seven, one ( Bolborhynchus orbignesius) was hitherto only known from Bolivia; two, so far as is yet ascertained, are peculiar to Tarapaca (namely Pheenicopterus jamesi and Aigialitis occidentalis), and the remaining four are Chilian species not hitherto recorded so far north. ' The species in the present collection from Tarapacd which have not yet been met with in Chili are 20 in number, namely :— Zurdus 1 ©Reise durch die Wiiste Atacama,’ &e. vy. Dr. R. A. Philippi: Halle, 1860. 26* 396 MR. P. L. SCLATER ON BIRDS [June 29, chiguanco, Phrygilus plebeius, Chrysomitris atrata, Sycalis uropygi- alis, Muscisaxicola albifrons, Centrites oreas, Cinclodes bifasciatus, Bolborhynchus orbignesius, Phoenicopterus andinus, P. jamesi, Me- triopelia aymara, Chamepelia cruziana, Gymnopelia erythrothoraz, Gallinula galeata, Fulica gigantea, F. ardesiaca, Vanellus resplen- dens, Aigialitis occidentalis, Recurvirostra andina, and Tinamotis pentlandi. VICINITY or TARAPACA CHILI Approximate altitudes shewnurteet, thurs 4,009 English Miles 05 2 30 40 50 To 72° 2° The sketch now exhibited (fig. 1) will show most of the different places in which the collection was formed. 1. Turpus cH1GuANCco, d’Orb. et Lafr. Turdus chiguanco, Seebohm, Cat. Birds B. M. v. p. 225; Sel. et Salv. P.Z. S. 1867, p. 984 (Islay). Merula chiguanco, Tacz. Orn. Per. ii. p. 494. Sibaya. One 9: iris brown; feet and beak vellow. Obtained by Whitely near Islay, Peru, in 1867. 1886. ] FROM TARAPACA, NORTHERN CHILI. 397 2. ANTHUS, sp, inc. Sacaya. One <¢: iris brown; feet brown; beak dark horn- colour. A young bird, nearest to A. furcatus, d’Orb. et Lafr. (Tacz. Orn. Pér. 1. p. 459). 3. ATTICORA CYANOLEUCA ( Vieill.). Atticora cyanoleuca, Sharpe, Cat. Birds B. M. x. p. 186; Tacz. Orn. Pér. i. p. 244. Huasco. One @ : iris brown; legs brown; feet black. 4, Puryerius arriceps (d’Orb. et Lafr.). Emberiza atriceps, d’Orb. et Lafr. Syn. Av. i. p. 76. Phrygilus atriceps, Tacz. Orn. Pér. ui. p. 34. Sacaya and Lalcalhuay. 5. PHRYGILUS UNICOLOR (d’Orb. et Lafr.). Emberiza unicolor, d’Orb. et Lafr. Syn. Av. i. p. 79. Phrygilus unicolor, Scl. et Salv. Nomencel. p. 31. Phrygilus rusticus, Tacz. Orn. Pér. iil. p. 38. Huasco. One 4G : iris dark brown. 6. ParyeGitus pLeBetvus, Tsch. Phrygilus plebeius, Scl. et Salv. Nomencl. p. 31; Taez. Orn. Pér. iii. p. 39. Huasco, Sitana, and Lalcalbuay. 7. PuRyGILus FRUTICETI (Kittl.). Phrygilus fruticeti, Scl. et Salv. Nomencl. p. 31; Tacz. Orn. Pér. iit. p. 37. Sibaya. One ¢: iris dark brown; feet yellowish. 8. Curysomitris aTrata (d’Orb. et Lafr.). Chrysomitus atrata, Scl. et Salv. Nomencl. p. 34; Taez. Orn. Pér. iii. p.'53. Huasco and Sacaya. Iris very dark brown. 9. Sycauis uropyGiALis (d’Orb. et Lafr.). Sycalis uropygialis, Scl. Ibis, 1872, p. 47; Tacz. Orn. Per, iii. p. 58. Huasco and Sitana. Three examples, ¢ et 2 : sexes alike. 10. Sycants AUREIVENTRIS, Ph. et Landb. as Sycalis aureiventris, Scl. Ibis, 1872, p. 47, pl. iii. Chumisa. One Q : iris dark brown. 11. Muscrsaxicoxa ALBIFrrons (Tsch.). Muscisaxicola albifrons, Tacz. Orn. Peér. ii. p. 209. Sacaya. One Q : iris dark brown; feet and beak black. 398 MR. P. L. SCLATER ON BIRDS [June 29, 12. MuscrsaxICOLA RUFIVERTEX; d’Orb. et Lafr. Muscisaxicola rufivertex, Tacz. Orn. Pér. ii. p. 216. Huasco. <¢ et 2: iris bright brown ; bill and feet black. 13. CENTRITES OREAS, Sel. et Salv. Centrites oreas, Tacz. Orn. Pér. il. p. 222. Sacaya. One ¢: iris very dark brown ; feet and beak black. 14. Grosirra cunrcuLanta (Vieill.). Geositta cunicularia juninensis, Tacz. Orn. Pér. ii. p. 93. Sacaya and Sitana. 6 et 9, alike: iris dark brown ; feet black ; beak horn-colour. 15. UpucertTHia RUFICAUDA (Meyen). Ochetorhynchus ruficaudus, Scl. P. Z.S. 1867, p. 324. Upucerthia ruficauda, Scl. et Salv. Nomencl. p. 62; id. P. Z.8. 1879, p. 619. Lalealhuay. ¢: iris brown; feet and beak black. 16. CINCLODES BIFASCIATUS. Cinclodes bifasciatus, Scl. P. Z.S. 1858, p. 448 ; Tacz. Orn. Per. il. p. 3. Upucerthia atacamensis, Phil. Reise d. d. Wiiste Atacaina, p. 161, t. ili. Chumisa, Sacaya, and Sibaya. Males: iris dark brown; feet and beak black. 17. Crnctopes Fuscus (Vieill.). Cinclodes fuscus, Scl. et Salv. P. Z. 8. 1867, p. 985. Cinclodes rivularis, Tacz. Orn. Pér, ii. p. 112. Chumisa, Cueva negra, and Sacaya. Iris brown ; feet black. 18, LeprastHENURA £GITHALOIDES (Kittl.). Leptasthenura egithaloides, Tacz. Orn. Pér. ii. p. 120. Huasco. Iris dark brown. 19. SyNALLAXIS MODESTA, Eyton. Synallaxis modesta, Scl. P. Z. 8. 1874, p. 23. Sacaya and Sitana. Two ¢ et 9: iris dark brown. 20. OREOTROCHILUS LEUCOPLEURUS, Gould. Oreotrochilus leucopleurus, Tacz. Orn. Per. ii. p. 278; Gould, Mon. Troch. i. pl. 71. Chumisa and Lalealhuay. Two females, with nest and eggs. The nest consists of an oblong mass of grey and brown wool (apparently Llama’s), with a few bits of moss intermixed. It is pointed at the lower extremity. In a shallow open depression are two white pyriform eggs ; they measure about 0°7 by 0°45 inch. 1886. ] FROM TARAPACA, NORTHERN CHILI. 399 21. BoLBORHYNCHUS ORBIGNESIUS. Myicpsitta orbignesia, Bp. Rev. et Mag. de Zool. 1854, p. 151. Bolborhynchus orbignesius, Scl. et Salv. P. Z.S. 1879, p. 635. Bolborhynchus @ orbigni, Finsch, Papag. ii. p. 129. Lalealhuay. Males and females: sexes alike; iris dark brown. These specimens agree with Bolivian skins of this little-known species. 22. BuTEo ERYTHRONOTUs (King). Buteo erythronotus, Tacz. Orn. Pér. i. p. 115. Lalcalhuay. @ : iris brown; feet yellow. 23. MILVAGO MEGALOPTERUS (Meyen). Milvago megalopterus, Tacz. Orn. Pér. i. p. 101. Sitana. d: iris brown; feet yellow. 24. ARDEA CANDIDISSIMA (Gm.). Ardea candidissima, Tacz. Orn. Pér. iii. p. 393. Sitana. d : iris yellow; feet black. 25. PH@NICOPTERUS ANDINUS, Philippi. Phenicopterus andinus, Philippi, Reise d. d. Wiiste Atacama, p- 164, tt. iv., v.; Tacz. Orn. Pér. iii. p. 423. Huasco. Two females, in full plumage. “ Iris very dark brown ; feet whitish yellow ; beak, fore part black, hind part whitish yellow ; between the nostrils brick-red ; lowest hinder part of lower mandible and a small spot before the eyes violet.” An egg is of a uniform chalky white, with irregular adherent chalky layers, as in some Cormorants’ eggs. It measures 3°6 by 2:1 inches, and is only slightly more pointed at the small end. 26. PuHa@NICOPTERUS JAMESI, sp. nov. (Plate XXXVI.) Ph. albus, capite colloque superiore et alis extus roseo indutis ; cervicis undique, dorsi superioris et pectoris plumarum apicibus cum scapularibus et secundariis externis elongatis et subalaribus sanguineo-rosaceis ; remigibus nigerrimis ; subalaribus longis sanguineis; pedibus rubris; rostri basi flava, apice nigra; loris nudis in pelle carneis; digito postico nullo: long. tota circ. 36°0, ale 16°0, caud@e 6°5, tarsi 8°0. Hab. in Andibus, prov. Tarapacensis. Obs. A Ph. andino cui pedibus tridactylis affinis, forma et pictura rostri, scapularibus et secundariis productis, et pedibus rubris sané diversus. An adult male in full dress and a male and female not in full dress of this new species of three-toed Flamingo were obtained by Rahmer at Sitana, at a height of about 12,000 feet, at the foot of the Voleano Tsluga. In a letter announcing this discovery, Mr. Rahmer has proposed to call the species ‘ jamesi,” a name which I adopt with great pleasure. 400 MR. P. L. SCLATER ON BIRDS [June 29; There can be no question. about the distinctness of this species from P. andinus. Besides the differences specified above, the confor- mation of the bill is of itself sufficient to render Ph. jamesi distinct in all ages. As will be seen by the sketches now exhibited (figs. 2 Fig. 2. Bill of Ph. andinus. Fig. 3. Bill of Ph. jamesi. and 3), the bill is much shorter and smaller in PA. jamesi, the naked space at the lores wider and differently shaped, and the upper mandible is much narrower. The very different disposition of the colours will be likewise seen from the figures. In P. jamesi the terminal black portion is much smaller, and is succeeded by an P28. 1886. PL. XXXVI. J.&Keulemans lth . PHENICOPTERUS JAMESI . 1886. ] FROM TARAPACA, NORTHERN CHILI. 401 orange-yellow which occupies the whole basal portion, while the narrow rim at the front, the lores, and the naked skin round the eye are red, in life (according to Rahmer) “ carmine.” . There is besides a red spot terminating the yellow at the front of the upper mandible. In P. andinus the black terminal portion is much more extended ; this is succeeded by a pale or “ whitish yellow” base ; and the part between the nostrils is “ brick-red.”” The lower part of the gonys next to the feathering and the narrow naked lores are in the skin of a flesh-colour, in life ‘* violet.”’ In P. jamesi the legs are red, in life ‘‘ carmine ;” in P. andinus ** whitish yellow.” In P. jamesi, as will be seen in the figure (Plate XXXVI.), the external secondaries are elongated into filiform plumes, which extend, when the wing is closed, as much as two inches beyond the primaries, and scapularies are similarly lengthened. Both these sets of plumes are of abright rosy red. This is also apparent in the two younger specimens of P. jamesi, but nothing of the sort appears to take place in P. andinus. 27. BERNICLA MELANOPTERA (Eyton). Bernicla melanoptera, Tacz. Orn. Pér- iii. p. 467. Sacaya. One adult and two nestlings: iris dark brown with a white rim; feet carmine. 28. ANAS CRISTATA, Gm. Anas cristata, Tacz. Orn. Pér. iii. p. 473. Sitana, Sacaya, and Huasco. Examples of both sexes: “iris orange.” A series of eight eggs are of the usual colour of Ducks’ eggs, a pale fulvous white ; they measure about 2°6 by 1:7 inch. 29. QUERQUEDULA CYANOPTERA (Vieill.). Querquedula cyanoptera, Tacz. Orn. Peér. iii. p. 475. Sitana and Sacaya. Examples of both sexes; iris orange. 30. QUERQUEDULA OXyYPTERA (Meyen). Querquedula oxyptera, Scl. et Salv. P. Z.S. 1876, p. 385 ; Tacz. Orn. Peér. iii. p. 477. Sitana, Sacaya, Huasco, and Lalealhuay. Males and females: iris dark brown. Ten eggs of this Duck accompany the skins ; they are duller and smaller than those of Anas cristata, and measure about 2°3 by 1°5 inch, 31. QuERQUEDULA PUNA (Tsch.). Querquedula puna, Tacz. Orn. Pér. iii. p. 478; Sel. et Salv, Ex. Orn, pl. xcix. Sitana and Sacaya. Examples of both sexes: ‘‘iris brown.” Five eggs are larger and more pointed than those of Q. owyptera and of a pale fulvous white. They measure about 2°3 by 1:75 inch. 402 MR. P. L. SCLATER ON BIRDS (June 29, 32. DariLa spinicauDA (Vieill.). Dafila spinicauda, Tacz. Orn. Pér. ii. p. 481. Sitana. A pair: “iris brown.” 33. METRIOPELIA MELANOPTERA (Gm.). Metriopelia melanoptera, Tacz. Orn. Pér. iii. p. 239. Lalcalhuay. A o: “iris dark blue; feet black.” 34. MerriopeLia AYMARA (d’Orb.). Metriopelia aymara, Tacz. Orn. Pér. iii. p. 240. Huasco and Sitana. Examples of both sexes: iris black or very dark brown ; feet flesh-coloured. 35. MeLopetia MELOoDA (Tsch.). Melopelia meloda, Tacz. Orn. Pér. iii. p. 241. Pica. A single specimen: “iris brown; feet carmine; beak black.” 36. CHAM#PELIA CRUZIANA (d’Orb.). Chamepelia cruziana, Tacz. Orn. Per. ili. p. 248. Pica. Examples of both sexes: ‘‘iris dark red, with white rim ; feet brick-red.”’ 37. GYMNOPELIA ERYTHROTHORAX (Meyen). Gymnopelia erythrothorax, Tacz. Orn. Pér. iii. p. 249. Sibaya. A young male: “‘ris light blue ; feet flesh-colour; naked skin round the eye orange.” 38. GALLINULA GALEATA (Licht.). Gallinula galeata, Tacz. Orn. Pér. iii. p. 327. Sitana. A single skin: “iris brown.” 39. Furica cicantea, Eyd. et Soul. Fulica gigantea, Tacz. Orn. Peér. iii. p. 329. Cueva negra near Sacaya. Four examples, all females: “‘iris red- brown ; feet dark brickdust-red ; bill red-brown, with the ridge and point white, and a spot on each side yellow.” Two eggs of this species are of the usual character of this group : they are of a pale stone-colour, sparingly spotted and speckled with two shades of reddish grey, and measure about 2°8 by 18 inch. 40. Fuxica ArpeEsrAca, Tsch. Fulica ardesiaca, Tacz. Orn. Pér. iii. p. 328; Scl. et Salv. Ex. Orn. pl. lvii. Huasco. Examples of both sexes, alike: ‘iris brown-red ; feet yellowish green ; joints and edges of toes greyish; bill with the ridge and borders of mandible white, the point yellowish green, and a spot near nostrils yellow ; blaze chocolate.” 1886.] FROM TARAPACA, NORTHERN CHILI. 403 41. Furica teucoptera, Vieill. Fulica leucoptera, Scl. et Salv. Ex. Orn. p. 119, pl. Ix. Fulica chloropoides, Landb. Wiegm. Arch. 1862, pt. i. p. 218. Fulica stricklandi, Hart). J. f. O. 1853, Extrah. p. 86. Huasco. One @: “iris red-brown; feet and bill yellowish green ; ridge of bill white ; spot near nostrils yellow; spot above the beak chocolate.” 42. VANELLUS RESPLENDENS (Tsch.). Vanellus resplendens, Tacz. Orn. Pér. iii. p. 336. Sitana and Sacaya. Three males, two females; sexes alike: iris carmine ; beak and feet carmine ; point of beak black. Neither Tschudi nor Taczanowski appear to have noted that there is no hind toe in this species. 43. ANGIALITIS OCCIDENTALIS, Cab. Aigialitis occidentalis, Cab. J. f. O. 1872, p. 158, et 1885, pl. vi. fig. 1 (head). Sitana, Huasco, and Cueva negra. Examples of both sexes: “iris brown ; feet black.” Mr. Seebohm has kindly determined these specimens, and sends me the subjoined remarks :— «* Although Cabanis gives no locality, nor mentions the colour of the legs and feet, there can be no doubt that his name refers to this species. He says it is a larger bird than 4. nivosus, but like it has white lores. He also refers to the rusty hind head and neck. “Tt appears to be the South-American representative of 4. rufi- capillus, which inhabits the coasts of Australia, Tasmania, and occasionally New Zealand.” 44. OrEOPHILUS RUFICOLLIS (Wagl.). Oreophilus ruficollis, Tacz. Orn. Pér. iii. p. 347. Lalealhuay. One ¢: iris dark brown; bill black; feet carmine. 45. THINOCORUS ORBIGNYANUS, Less. Thinocorus orbignyanus, Tacz. Orn. Per. iil. p. 281. Sacaya. Examples of both sexes: iris brown ; bill horn-colour ; feet yellow. Three eggs are much pointed, and call to mind those of the Gralle: they are of a shining buffy white, finely speckled with greater and lesser black and blackish specks, and measure about 1-5 by 1-1. 46. PHEGorNIS MITCHELL, Fraser. Leptopus mitchelli, Fraser, P. Z. 8S. 1844, p. 157. Phegornis mitchelli, Tacz. Orn. Pér. iii. p. 372. Sitana. One ¢: “iris dark brown, almost black; feet yel- lowish ; beak black.’’ 404 ON BIRDS FROM TARAPACA, NORTHERN CHILI. [June 29, A scarce bird, originally described from Chili, where Philippi says it is found on the high Cordillera of the Central Provinces *. The same naturalist also obtained it near Rio Frio in the desert of Atacama (Reise d. d. Wiiste Atacama, p. 163). Jelski met with it on the Lake of Junin, Central Peru. 47, RecurVIROSTRA ANDINA, Ph. et Landb Wiegm. Arch. 1863, pt. i. p. 131; Harting, Ibis, 1874, p. 257, pl. ix. Three examples of this scarce bird from Huasco. “Iris orange with a yellow rim ; legs bluish grey ; beak black.” 48. TrRINGA MACULATA, Vieill. Tringa maculata, Tacz. Orn. Pér. iti. p. 356. Huasco. “Iris light brown.” 49. TRINGA BarIRDI (Coues). Tringa bairdi, Tacz. Orn. Pér. iii. p. 359. Huasco, Sacaya, and Cueva negra. “ Iris dark brown.” 50. GAMBETTA MELANOLEUCA (Vieill.). Totanus melanoleucus, Tacz. Orn. Per. iii. p. 365. Sitana. 51. GAMBETTA FLAVIPES (Gm.). Totanus flavipes, Tacz. Orn. Pér. iii. p. 367. Sacaya. 52. Larus SERRANUS, Tsch. Larus serranus, Tacz. Orn. Pér. iii. p. 452. Huasco, Sitani, and Cuevanegra. Examples of both sexes: “iris dark brown; bill and feet dark brown-red.” 53. TINAMOTIS PENTLANDI, Vig. Tinamotis pentlandi, Tacz. Orn. Pér. iii. p. 310. Huasco. One ¢: ‘‘iris chocolate; legs whitish greenish ; feet black.”’ ? “Cat. Ay. Chilenas,” in Anales de la Univers. de Chile, tom. xxxi. p. 272. 1886. ] ON THE COLUMELLA OF ICHTHYOSAURUS. 405 10. Note on the Presence of a Columella (Epipterygoid) in the Skull of Ichthyosaurus. By A. Smrra Woopwarp, F.G.S., of the British Museum (Natural History). (Communicated by Professor Frowrr, LL.D., F.R.S., President.) [Received June 3, 1886.] In the skulls of fossil Reptiles and Amphibia it so rarely happens that the bones on the inner side of the temporal fossa, and those between the orbits, are well exposed to view, that even in some of the most familiar genera very little has yet been ascertained regarding the special characters of any of these ossifications. In so conspicuous a form as Ichthyosaurus, for example, there appears to be no published reference to these structures beyond the brief statements of Profs. Huxley, Cope, and Sir Richard Owen, and even these do not afford any very definite information. Prof. Huxley determined’ the presence of a distinct pro-otic, and the doubtful absence of ali- and orbito-sphenoids ; Prof. Cope gives* a diagrammatic outline of the “ columella” ; while Sir Richard Owen appears to have been less successful in his researches, having met with nothing but unsatisfac-. tory indications of small ‘‘alisphenoids” (? pro-otics), and especially remarking that there is “ no trace or sign of the Lacertian columellar bone”’’. ; In making the latter statement, the distinguished paleontologist just mentioned evidently overlooked Prof. Cope’s previous researches upon the osteology of the Ichthyosaurian skull; and having lately discovered that there is no foundation for the assertion in the British Museum specimens, that formed the basis of Sir Richard Owen’s monograph, I venture to offer a few remarks upon the subject, by way of pointing out the mistake. A detailed description of the interesting bone in question may also be acceptable, since Prof. Cope’s materials appear to have been less complete and satisfactory than those now afforded by the fossils from the English Jurassic. The first specimen of interest in this connection is a small slab of Lias from Lyme Regis, exhibiting a number of dislocated cranial bones, which Mr. William Davies long ago recognized as belonging to Ichthyosaurus, but which do not appear, hitherto, to have been submitted to so careful a study as their admirable state of preserva- tion renders desirable. In the middle of the fossil, the basioccipital, basisphenoid, and presphenoid are arranged in irregular series, with their upper aspect exposed ; in front are the remains of the supra- occipital and parietals ; and on either side are scattered a number of 1 'T. H. Huxley, ‘ Anatomy of Vertebrated Animals,’ 1871, p. 211. 2 B. D. Cope, “ On the Cranium of the Ichthyopterygia,” Proc. Amer. Assoc. Adv. Sci. vol. xix. (1870), pp 200-203. (For this reference I am indebted to the kindness of Mr. J. W. Hulke, F.R.S.) 3 R. Owen, “ Fossil Reptilia of the Liassic Formations.—IIT.” (Mon. Pal, Soc. 1881), p. 96; also, ‘ History of British Fossil Reptiles, vol. ii. (1884), p. 54. 406 MR. A. SMITH WOODWARD ON THE [June 29, other cranial elements in a more or less well-preserved state. Among the latter are two long bones with expanded extremities, lying lengthwise, one on either side of the basi- and presphenoids; and the form and situation of these elements, considered in connection with the evidence of other specimens presently to be noticed, can leave no doubt that they are the homologues of the columella (epipterygoid, Parker) found in Lacertilia, Khynchocephalia, Ano- modontia, Dinosauria*, and Chelonia. ‘The bone on the right shows a side view, while that on the left is seen either from behind or before, and although both are fractured to a certain extent, their boundaries are readily distinguishable. The right columella is 0°045 metre in total length, and is shown of the natural size in fig. 1*(p. 407). The upper end exhibits a tri- angular expansion, which, before fracture, must have measured about 0-016 metre in greatest breadth ; and the long terminal upper border thus produced has a gently arched contour. Immediately below the expanded portion the bone becomes much constricted, having a diameter of only 0°003 metre, and at the distance of 0°019 metre from the lower extremity it commences again to widen, but here in am unsymmetrical manner. From the upper expansion downwards the anterior edge is nearly straight, but at the point just mentioned the hinder edge rapidly curves backwards, until the bone attains a maximum breadth of 0°012 metre, when the border once more descends almost vertically for some distance, and finally curves to the front. The lower end, however, has evidently been much crushed, like the remainder of the bone, and perhaps does not give an exact idea of its original shape. The left columella, presenting only an anterior (or hinder) view, does not add any further details to the foregoing description ; but this side of the fossil is of especial interest, since, as pointed out to me by Mr. G. B. Howes, there appears to be some indication of a downwardly-directed process of the parietal to meet the columella, such as exists in the living Cyclodus*. There is no indication of the fusion of the upper end of the bone with the parietal (or ? “squamosal”’), such as Prof. Cope describes (/. ce. p. 204) in the American form. In a skeleton of Jchthyosaurus from the collection of the late Prof. Tennant (No. R 44 of the B.M. Register), the postorbital and adjoining bones are so far removed and displaced as to permit an admirable view of the lower end of the right columella, which is uncrushed, and still in contact with the pterygoid immediately behind the orbit. This is shown of the natural size in fig. 2. Its front edge is almost vertical, but curves slightly forwards near the lower termination, and there is a sharp anterior outer ridge along the whole length of the bone. The expanded portion exhibits a 1 See O. C. Marsh, “ Restoration of Brontosawrus,” Amer. Journ. Scix(3) vol, xxvi. p. 83; ‘On the Diplodocide,” zbid. (3) xxvii. p. 163; “The Order Theropoda,” tom. cit. p. 332. ? The drawings have been made by Mr. W. H. Hill. 3 T. H. Huxley, ‘ Anatomy of Vertebrated Animals,’ p. 189, fig. 69. 1886.] COLUMELLA OF I[CHTHYOSAURUS. 407 long inferior border, decidedly marked off from a short posterior border, but the precise nature of its original articulation is unfortu- nately not apparent. The pterygoid seems to have slipped some- what from its natural position. Fig. I. Fig. 2. Fig. 1. Right columella of Zchthyosawrus, much crushed ; inner side view. [B.M., No. 2000. 40 * .] Fig. 2. Lower portion of right columella of Jchthyosaurus; outer side view : pi, pterygoid ; 0, crushed bones in orbit. [B.M., No. R 44.] Fig. 3. Lower portion of left columella of Ichthyosaurus intermedius; inner side view. [B.M., No. 2000. 15.] Fig. 4. Left columella of Hatteria punctata; outer side view: pt, pterygoid ; gu, quadrate. The fragmentary skull of Zchthyosaurus’ figured by Hawkins in his ‘ Book of the Great Sea-Dragons,’ pl. 19. fig. 1, also exhibits the lower two thirds of the left columella, and this is interesting as * This specimen has been identified with Z, intermedius, Conyb., by Sir Richard Owen, and bears his MS8, label, 408 ON THE COLUMELLA OF ICHTHYOSAURUS. [June 29, displaying an uncrushed inner view: the bone, however, though well shown in Mr. O’Neill’s drawing, is not specially marked, and it is therefore advisable to append a separate sketch, such as is given in the woodcut, fig. 3 (p. 407). The general outline is similar to that of the examples already described, but the additional characters of the inner aspect are well worthy of note. In the constricted portion of the bone, the shaft is compressed to form a sharp ridge, which terminates in an abrupt prominence at the point where the lower expansion commences, and beneath this the broad surface is divided into two distinct, apparently articular, facettes. The upper and hinder division (a) is slightly hollowed and somewhat triangular in shape ; while the lower facette (4) is more elongated, and is separated from the first in its anterior portion by being more deeply impressed in the bone. Among the crushed cranial bones, immediately behind the sclerotic plates, in another specimen of JeAthyosaurus in the National Collec- tion the culumella is also distinctly visible; but this does not supply any additional facts of importance. On comparing the bone under consideration with its homologue among recent Reptiles, none is found to exhibit a more striking similarity than that of Hatteria (fig. 4, p. 407). As Dr. Ginther has pointed out’, the columella in this genus is particularly remarkable for the great expansion of its extremities ; and it is also peculiar from the fact that the lower end articulates not only with the pterygoid, but also with an inward extension of the quadrate. Moreover, so far as can be ascertained from a complete skull, the columella appears to show some signs of contracting this articulation by an overlapping of the two bones in a vertical plane; and the upper end is connected with cartilage, and not directly in contact with the parietal above. Unfortunately at present it is only possible to compare the form of the element in each of these types. In none of the fossil Ichthyo- saurs 1 have examined are the precise relations of the bone very distinct. As already stated, however, the first fossil is remarkably suggestive of a direct articulation of the upper end of thecolumella with a downward process of the parietal ; and the originals of figs. 2 and 3 exhibit so close a resemblance to the corresponding parts in Hatleria, that there is also strong evidence of the lower articulation being double. But it ought to be remarked that in Ichthyosaurus no inwardly directed extension of the quadrate has hitherto been observed *, and the discovery of more satisfactory specimens must yet be awaited before it is possible to arrive at any definite conclusion. 1 A. Giinther, “Contribution to the Anatomy of Hatteria (Rhynchocephalus, Owen),” Phil. Trans. 1867, p. 599, pl. xxvi. figs. 3, 4. * Hi. G. Seeley, “ Similitudes of the Bones in the Enaliosauria,” Journ. Linn. Soe. (Zoology) vol. xii. (1876), p. 309. 1886.] ON NEW HETEROCERA FROM TROPICAL AFRICA. 409 11. Descriptions of some new Species of Heterocera from Tropical Africa. By Hersert Drvce, F.L.S., F.R.G.S., F.Z.S. [Received June 16, 1886.] (Plates XXXVII. & XXXVIII.) SATURNIIDS. ATTACUS ALBIDUS, sp. n. (Plate XX XVII. fig. 1.) 3. The primaries very similar to A. ploetzi, but the white band is closer to the outer margin, four round white spots between the apex and the anal angle. Secondaries pure white excepting the outer margin, which is narrowly bordered with reddish brown, with black and fawn-coloured lunular markings as in A. ploetzi; the vitreous spot long, narrowly edged with black, bordered on the inner side with yellow. The underside the same as above. Head and thorax reddish brown, a wide white band at the base of the thorax, the abdomen brown banded with white; antenne and legs pale yellowish brown. The female the same as the male, but slightly more reddish in colour, and with all the vitreous spots considerably larger. Expanse, ¢ 7 inches, 2 63 inches. Hab. West Africa, Cameroon Mountains. Mus. Druce. This very fine species comes into the group containing A. vacuna, Westw., A. ploetzi, Weymer, from both of which it is at once distin- guished by the pure white secondaries. ANTHERHA DOLABELLA, sp. n. (Plate XXXVIII. fig. 2, ¢.) 3. Primaries chrome-yellow, crossed by three irregular black bands, beyond which, along the outer margin, are a series of dusky patches, the base of the wing shaded with pink. Secondaries bright pink, broadly bordered with chrome-yellow, from the apex to the anal angle with several indistinct dusky black patches; nearest the anal angle a wide black band, dividing the two colours, crossing from near the apex to the inner margin; a large round deep yellow ocellus with a wide black border, on the outer edge of the black is a ring of bluish-fawn colour ; in the centre of the ocellus is a very small vitreous spot. Head and thorax and upperside of abdomen bright pink, the underside of abdomen chrome-yellow banded with black ; tegulee chrome-yellow ; antennz black; legs black and yellow. Expanse 44 inches. Hab. East Central Africa. Mus. Druce. This very beautiful species is quite unlike any other known to me. Buna pyGELa, n. sp, (Plate XXXVIII. fig. 1, ¢.) 3. Primaries uniform pale pinkish brown, darkest along the costal margin; the outer and inner margin narrowly edged with pink ; underside as above, but shaded with dark yellow from the base to about the middle; a small black spot at the end of the Proc. Zoo. Soc.—1886, No. XXVII. 27. 410 ON NEW HETEROCERA FROM TROPICAL AFRICA. [June 29, cell. Secondaries dark orange-yellow, bordered from the apex to the anal angle and thence along the inner margin to the base with bright pink; a large central round fawn-coloured ocellus broadly edged with black. The underside uniform pale pinkish brown. Head and thorax orange-yellow ; collar and underside of the thorax pure white ; a wide pink band at the base of the thorax. Abdomen, upperside orange-yellow, underside pale pinkish brown; the anus pink ; antennz brown, deeply pectinated ; legs pale brown. Expanse 33 inches. Hab. East Africa, Matebele Country. Mus. Druce. This species is allied to B. pygmea, Maassen, from which it is at once distinguished by not having the black band across the pri- maries and the absence of the white dot at the end of the cell, and difference in the colour of the antenne. LASIOCAMPIDE. STIBOLEPIS SYLVIA, sp. nN. Primaries silvery white, brownish black along the costal margin, the apex, and outer margin; the veins from the cell to the onter margin dusky. Secondaries silvery white, with the apex and outer margin narrowly edged with brownish black ; the veins a short way up from the margin dusky. . Underside as above, excepting that the primaries have less black at the apex. Head and thorax yellowish white. Abdomen dark yellow; antenne black; legs yellow. Expanse 27 inches. Hab. West Africa, Cameroons (Thompson). Mus. Druce. This beautiful species is allied to Stibolepis nivea, Butler, from which it is at once distinguished by its smaller size and entire absence of the black marginal band of that species. CHRYSOPOLOMA ROSEA, sp.n. (Plate XXXVIII. fig. 3.) Primaries fawn-colour, shaded with pink along the inner margin, crossed beyond the middle by a row of brownish-red spots. Secon- daries pale yellow, the fringe pinkish. The head, thorax, and abdomen pale yellowish-fawn colour ; legs brownish black ; antenne black. Expanse 1? inch. Hab. Fast Africa, Delagoa Bay. Mus. Druce. This pretty little species is allied to Chrysopoloma obtusa, Walker, also from East A{rica. CHRYSOPOLOMA CITRINA, Sp.n. (Plate XXXVIII. fig. 4.) Primaries pale yellow, crossed about the middle, from the costal to the inner margin, by a band of very small brown spots, beyond which is a second band, extending from the apex to the inner margin ; the second band is very much wider, and near the inner margin it has several whitish spots; a submarginal row of minute dots extending from the apex to the anal angle. Secondaries pale yellow, with a central and submarginal row of small brown spots. The fringe of both primaries and secondaries pale yellow; the underside uyly sstyand Af LVek : oe JVi P.Z.5.1886 Pl. XXAVITI Hanhart imp W.Purkrss. lith 1. BUNAEA PYGELA. 2 ANTHEREA DOLABELLA. 3 CHRYSOPOLOMA ROSEA. 4CHRYSOPOLOMA CITRINA® 1886.] BATRACHIANS IN THE NATURAL-HISTORY MUSEUM. 4/1 uniform pale yellow. Head, thorax, and abdomen yellow; legs yellow, banded with brown. Expanse 1{ inch. Hab. West Africa, Old Calabar. Mus. Druce. In form this species resembles C. rudis, Walker, but in colour and markings it is very distinct. LECHENOPTERYX FULVIA, Sp. 0. Primaries pinkish brown, crossed near the outer margin from near the apex to the inner margin by a_ black line, bordered on the inner side with yellow ; a small white dot edged with black at the end of the cell; secondaries pinkish brown, with the same coloured line extending from the apex to the inner margin close to the anal angle. Underside much paler than above, and the black lines not edged with yellow. Head, thorax, and abdomen pinkish brown ; antennee brown; legs darker brown. Expanse 13 inch. Hab, East Africa; Zanzibar. Magila (Craven). Mus. Druce. EXPLANATION OF THE PLATES. Puare XXXVII. Fig. 1. Attacus albidus, sp.n., 3, p. £09. Prats XXXVIII. Hig. 1. Bunea pygela, sp.n., 3, p. 409. 2. Antherea dolabella, sp.n., 3, p. 409. 3. Chrysopoloma rosea, sp. u., p. 410. 4. citrina, sp.n., p. 410. 12. First Report on Additions to the Batrachian Collection in the Natural-History Museum. By G. A. Bov- LENGER. [Received June 28, 1886.] (Plate XXXIX.) The following is a list of all the species of Batrachians added to the National Collection since the publication of the last edition of the Catalogue (1882). ‘To such names as are not mentioned in that work, reference to the original description is appended ; an asterisk indicates that the type specimen is in the collection. ‘The list is followed by the descriptions of a few new species. ECAUDATA. *1. Ceratobatrachus guentheri, Blgr. P. Z.8. 1884, p. 212.— Solomon Islands (Guppy). *2. Rana bufoniformis, Blgr. |.c. p. 210.—Solomons (Guppy). *3. Rana sternosiynata, Murray, Ann. N. H. (5) 1885, xvi. p- 120. —Sind (Murray). *4. Rana guppyi, Bigr. 1. c. p. 211—Solomons (Guppy). *5. Rana opisthodon, Blgr. 1. c. p. 211.—Solomons (Guppy). 6, Rana septentrionalis, Baird.—Canada (Lataste). 412 MR. G. A. BOULENGER ON BATRACHIANS [June 29, *7. Rana forreri, Blgr. Ann. N. H. (5) 1883, xi. p. 343.— Presidio, W. Mexico (Forrer). *8. Rana macrocnemis, Blgr. P. Z.S. 1885, p. 22.—Brusa (v. Maltzan). 9. Rana iberica, Blgr.—Serra de Gerez, Portugal (Gadow). 10. Rana latastii, Blgr.—Various localities in North Italy (Camerano and de Betta). *11. Rana martensi, Blgr., infra.— Yedo (v. Martens). *12. Rana pustulosa, Blgr. Ann. N. H. (5) 1883, xi. p. 343.— Ventanas, W. Mexico (forrer). 13. Rana nicobariensis, Stol.—Nias (Sandemann). *14, Rana masonii, Blgr. Ann. N. H. (5) 1884, xiii. p. 397,— Batavia (Mason). *15. Rana macropus, Blgr., infra.—Loo Choo Islands ( Carpenter). 16. Rana ulcerosa, Bttg.—Nossi Bé (Senckenberg Mus.). 17. Rana granulata, Bttg—Nosi Bé (Senckenberg Mus.). 18. Rana buergeri, Schleg—Japan (Anderson). 19. Rhacophorus dispar, Bttg.—Nossi Bé (Senckenberg Mus.). *20. Rhacophorus lateralis, Blgr. Aun. N. H. (5) 1883, xu. p- 162.—Malabar (Beddome). *21. Ivalus asper, Blgr., infra—Larut, Perak (Wray). *22. Cornufer guppyi, Bigr. P. Z.S. 1884, p. 211.—Solomons (Guppy). *23. Cornufer solomonis, Blgr. 1. c. p. 212.—Solomons (Guppy). *24, Rappia burtonii, Blgr. Aun. N. H. (5) 1883, xii. p. 163.— Gold Coast (Burton and Cameron). 25. Nyctizalus margaritifer, Blgr. Aun. N. H. (5) 1882, x. p- 35.—Willis Mountains, Java (v. Huegel). *26. Prostherapis femoralis, Blgr. P.Z.S. 1883, p. 635.— Yurimaguas (Hahnel). 27. Mantella ebenaui, Bttg.—Nossi Bé (Senckenberg Mus.). *28. Dendrobates reticulatus, Blgr. |. c. p. 635.—Yurimaguas (Hahnel). *29, Dendrobates fantasticus, Blgr. |. c. p. 636.—Yurimaguas (Hahnel). *30. Dendrobates hahnelii, Blgr. 1. c. p. 636.—Yurimaguas (Hahnel). *31. Hypopachus oxyrrhinus, Blgr. Ann. N. H. (5) 1883, xii. p. 344.—Presidio (Forrer). *32. Microhyla fissipes, Blgr. Ann. N. H. (5) 1884, xiii. p- 397.—Taiwanfoo, Formosa. 33. Rhombophryne testudo, Bttg.— Nossi Bé (Senckenberg Mus.). 34. Cophyla phyllodactyla, Bitg.—Nossi Bé (Senckenberg Mus.). 35. Pseudis mantidactyla, Cope-—Rio Grande do Sul (v. Ihering). Montevideo (Paris Mus.). KR. de la Plata (Gairdner). *36. Phyllobates trilineatus, Blgr. P. Z.S. 1883, p. 636.—Yuri- maguas (Hahzel). 37. Hylodes brocchii, Blgr. in Brocchi, Miss. Se. Mex., Batr. p- 60.—Vera Paz (Salvin). 38. Hylodes augusti, Brocchi.—Ventanas ( Forrer). 1886.] #39. . Paludicola gracilis, Blgr. Ann. N. H. (5) 1883, xi. p. 17.— IN THE NATURAL-HISTORY MUSEUM. 413 Hylodes vertebralis, Blgr., infra.—Intac, Ecuador ( Buckley). Rio Grande do Sul (v. Ihering). Uruguay. . Paludicola falcipes, Hens.—R. Grande do Sul (v. Ihering). . Paludicola olfersii, Martens, Nomencl. Rept. Mus. Berol. p- 40.—Brazil (Berlin Museum). . Leptodactylus discodactylus, Blgr. P. Z. 8. 1883, p. 637.— Yurimaguas (Hahnel). . Leptodactylus gracilis, D. & B—Rio Grande do Sul (». Ihering). . Leptodactylus rhodomystaz, Blgr. 1. ec. p. 637.—Yurimaguas (Hahnel). . Leptodactylus diptyx, Bttg. Zeitschr. f. Naturw. 1885, lviii. p- 244.—Paraguay. . Limnodynastes olivaceus, De Vis, Proc. Linn. Soc. N. 8S. W. 1884, ix. p. 66.—Queensland (Ling Roth). . Eupemphizx nattereri, Stdchr.—Paraguay. . Bufo mexicanus, Brocchi.—Ciudad (Forrer). . Bufo andersonii, Blgr. Aun. N. H. (5) 1883, xii. p. 163.— Ajmere and Muscat (Blanford). Tatta, Sind. . Bufo formosus, Blgr. P.Z.S. 1883, p. 140.—Yokohama (‘ Challenger ’). . Bufo punctatus, B. & G.—La Paz, Cal. (Smithson. Inst.). . Hyla nasica, Cope—Rio Grande do Sul (wv. Ihering). Soriano, Uruguay (Havers). Paraguay. . Hyla glandulosa, Blgr. Ann. N. H. (5) xii. 1883, p. 164.— Guatemala (Godman). . Hyla macrops, Blgr. |. c. p. 164.—Treasury Island, Solo- mons (Guppy). . Hyla thesaurensis, Ptrs.—Treasury Island (Guppy). . Hyla stoufferi, Cope.—Guatemala (Godman). . Pternohyla fodiens, Blgr. Ann. N. H. (5) 1882, x. p. 326.— Presidio (Forrer). . Phyllomedusa iheringii, Blgr. Ann. N. H. (5) 1885, xvi. p- 88.—Rio Grande do Sul (v. Thering). . Phyllomedusa perlata, Blgr. P. Z. 8. 1883, p. 638.—Yurima- guas (Hahnel). . Triprion spatulatus, Gthr. Aun. N. H. (5) 1882, x. p- 279.—Presidio (Forrer). . Scaphiopus couchii, Baird.—Presidio (Forrer). . Megalophrys longipes, Bigr. P. Z.S. 1885, p. 850.——Perak (Wray). CauDATA. *1. Hynobius lichenatus, Blgr. Ann. N. H. (5) 1883, xii. p- 165.—Awomori, Japan (Lewis). *2. Geomolge fischeri, Blgr., infra—Manchuria (Fischer). 3. Plethodon croceater, Cope.—San Diego, Cal. (Forrer). *4. Spelerpes peruvianus, Blgr. Ann. N. H. (5) 1883, xii. p. 165. —Moyobamba, Peru (Rof). 414 MR. G. A. BOULENGER ON BATRACHIANS — [June 29, Apopa. *1. Epicrionops bicolor, Blgr. Ann. N. H. (5) 1883, xi. p. 202.— Intac, Ecuador (Buckley). *2. Cecilia buckleyi, Blgr. Aun. N. H. (5) 1884, xiii. p. 398.— Intae (Buchley). 3. Dermophis thomensis, Bocage—S. Thomé (Berlin Mus.). *4,. Oryptopsophis multiplicatus, Blgr. Ann. N. H. (5) 1883, xii. p- 166.—Seychelles (Giinther). 5. Gymnopis unicolor, A. Dum.—Cayenne (Bavay). *6. Scolecomorphus kirkii, Blgr. Ann. N. H. (5) 1883, xi. p. 48.—Near Lake Tanganyika (Kirk). 7. Chthonerpeton indistinctum, R. & L.—Porto Alegre (Berlin Mus.). RANA MARTENSI, Sp. n. Allied to R. temporaria. Vomerine teeth in two rather oblique oval groups, extending posteriurly beyond the line of the choanze. Head about as long as broad, very similar to that of R. agilis ; nostril equally distant from the eye and the end of the snout; iuterorbital space narrower than the upper eyelids; tympanum rather large, its diameter equalling about two thirds that of the eye, from which it is separated by a space equal to about half its diameter. The first finger extends beyond the second. ‘The tibio- tarsal articulation reaches the eye or the nostril; tibia shorter than the fore limb. Inner metatarsal tubercle rather strong, blunt, oval ; outer tubercle absent, or scarcely marked ; subarticular tubercles of fingers and toes moderate ; toes two-thirds webbed. Skin smooth ; lateral fold rather narrow, moderately prominent. Coloration very similar to that of R. agilis, save that the whitish streak bordering the temporal spot inferiorly does not extend forwards beyond the eye. Male with internal vocal sacs. Yedo; several specimens (4410, 4411) in the Berlin Museum, one of which was obtained for the British Museum. Collected by Dr. E. von Martens (cf. Preuss. Exped. n. Ost-Asien, Zool. i. p. 111). RANA MACROPUS. Ivalus japonicus, Hallow. Proc. Ac. Philad. 1860, p. 501. Vomerine teeth in two rather indistinct oblique series between the choanze, widely separated in the middle. Snout obtuse, as long as the diameter of the orbit; nostril nearer the end of the snout than the eye; canthus rostralis well marked, curved; loreal region con- cave; eye large ; interorbital space narrower than the upper eyelid ; tympanum very distinct, measuring not quite half the diameter of the eye. Fingers moderate, slightly depressed, first shorter than second; toes moderate, three-fourths webbed; tips of fingers and toes dilated into well-developed disks, which are much smaller than the tympanum ; subarticular tubercles moderate ; a single, oval, inner metatarsal tubercle ; no tarsal fold. When the fore limb is stretched 1886.] IN THE NATURAL-HISTORY MUSEUM, 415 forwards, the femoro-tibial articulation reaches the shoulder and the tibio-tarsal far beyond the end of the snout; tibia as long as the fore limb. Upper surfaces with small warts intermixed with elon- gate fold-like ones, which form an )(-shaped figure on the scapular region; a strong fold from eye to shoulder. ‘Dark brown above, with darker marblings and regular cross bars on the limbs; lips with a series of dark brown spots ; lower surfaces white. From snout to vent 34 millim. A single (half-grown ?) specimen was obtained at Oho Sima, Loo Choo Islands, and presented to the Museum by Lieut. Alfred Carpenter, R.N., of H.M.S. ‘ Magpi:.’ IXALUs ASPER, sp.n. (Plate XXXIX. fig. 1.) Snout rounded, as long as the diameter of the orbit; canthus rostralis very feebly marked; loreal region concave; nostril nearer the tip of the snout than the eye; interorbital space broader than the upper eyelid; tympanum very distinct, nearly as large as the eye. Fingers free, toes three-fourths webbed ; disks well deve- loped; subarticular tubercles weak ; a small inner netaancel tubercle. The tibio-tarsal articulation reaches nearly the tip of the snout. Upper parts rough with small conical warts ; belly granular, throat perfectly smooth. Blackish above and below; the warts of the upper surfaces appearing as white dots; belly marbled with white; flanks, lower surface of limbs, and hinder side of thighs with irregular white network. Male without vocal sac. From snout to vent 35 millim. Two specimens, male and female, presented by L. Wray, Esq. ; caught breeding in the water on Hill Garden, Larut, Perak, at an altitude of 3300 feet. HyLopes VERTEBRALIS, Sp. Nn. Tongue oval, entire. Vomerine teeth in two oblique groups con- siderably behind the choanz. Snout rounded or subacuminate, as long as the greatest orbital diameter; canthus rostralis distinct ; nostril nearer the tip of the snout than the eye; fronto-parietals a little concave, their edges slightly prominent, their width equalling once and one third that of the upper eyelid; tympanum distinct, two fifths the diameter of the eye. Fingers moderate, first shorter than second ; toes moderate, quite free, fringed; disks quite as large as the tympanum; subarticular tubercles moderate; two metatarsal tubercles. The tibio-tarsal articulation reaches the eye. Back smooth, sides with small warts; belly granular. Blackish brown above; one specimen with a whitish vertebral band; lower surfaces yellow, brown-speckled ; groin and sides of thighs with dark-brown network. From snout to vent 38 millim. Two female specimens, from Intac, Ecuador; collected by Mr. Buckley. Distinguished from H. buchkleyi by a less stout habit, larger digital expansions, and narrower fronto-parietals. 416 BATRACHIANS IN THE NATURAL-HISTORY MUSEUM. [June 29, GEOMOLGE, g. n. Tongue large, subcircular, free on the sides. Palatine teeth in two arched, slizhtly angular series, separated by a narrow interspace. Toes five. Tail cylindrical at the base, compressed at the end. Intermediate between Onychodactylus and Ranidens in the pala- tine dentition; distinguished, besides, from the former by the absence of claws, from the latter by the shape of the tail, which indicates a land animal. GEOMOLGE FISCHER], sp.n. (Plate XXXIX. fig. 2.) Physiognomy that of Onychodactylus japonicus. Head small, longer than broad, broader than the neck; snout rounded; eyes large, prominent; no labial lobes. Body cylindrical, four al a half or five times the length of the head. Limbs in every respect similar to those of Onychodactylus japonicus, save the absence of claws; the male likewise with tibio-tarsal dilatation. Tail longer than head and body, cylindrical in its anterior half, becoming gradually compressed and keeled towards the end, which is obtusely pointed. Anal opening subcruciform, as in Onychodactylus. Skin smooth; fourteen or fifteen costal grooves; paratoids and gular fold as in Onychodactylus. Brown above, with blackish variegations, most crowded on the sides, which also bear some whitish spots; lower surfaces brownish white. ohhic oe millim. millim. Wotablenctlas, © if Misc ahs saree ce LOO — From snout to vent .............. 70 80 Head . Eta Tah Pais red. Syston inher meme 14 Wither hamden st: ees Aue 93 10 Poreclimb: stk es. Soe he eee a 20 ind ims? Seco A ot nee ee 22 Tale Mk ne arte a tole tet ee 8 hee —! Two specimens from Chaborowska, on the River Ussuri, Man- churia, collected by Hr. Dorries, of Hamburg; they were obtained for the British Museum through Dr. J. G. Fischer, in honour of whom the new species is named. EXPLANATION OF PLATE XXXIX. Fig.1. Jzalus asper, wpper view. la. , lower view. 2. Geomolge fischeri, 3: 2a. —, side view of head. 26, —— ——., open mouth. 1 Tail injured. PS PZ.S. 1886. Pl. XXXIX FW Frohawk del et Lith. Nintern Bros. unp 1. XALUS ASPER . 2. GEOMOLGE FISCHERI. 1886.] THE SECRETARY ON ADDITIONSTO THE MENAGERIE. 417 November 16, 1886, Prof. W. H. Flower, LL.D., F.R.S., President, in the Chair. The Secretary read the following reports on the additions made to the Society’s Menagerie during the months of June, July, August, September, and October, 1886 :— The total number of registered additions to the Society’s Mena- gerie during the month of June was 226, of which 24 were by birth, 129 by presentation, 52 by purchase, and 21 were received on _ deposit. The total number of departures during the same period by death and removals was 120. The following are of special interest :— 1. A Glaucous Macaw (dra glauca), purchased of the Zoological Gardens, Antwerp, June 3rd. Of this near ally of Lear’s Macaw’ we have not previously possessed a living specimen. The present species is of nearly the same size and general coloration as A. leari, but is at once distin- guishable by the glaucous blue of the body. 2. Two young Tcheli Monkeys (Macacus tcheliensis), presented by Dr. S. W. Bushell, C.M.Z.S., of Pekin, June 17th, obtained from the mountains near the “ Jung-ling,” or Eastern Mausoleum of the reigning dynasty of China, which is situated some 70 miles east of Pekin. The animals are covered with a thick fur, which fits them to endure the bitterly cold winter of this part of Northern China, where the thermometer frequently goes below zero of Fahrenheit. We are also indebted to Dr. Bushell for former examples of this Monkey. 3. A Bald Ouakari (Brachyurus calous), 3 , purchased 12th June, of a dealer in Liverpool, new to the Society’s collection. Of the curious Monkeys of the genus Brachyurus, on which our late Prosector, Mr. Forbes, wrote an excellent paper in 1880 (see P. Z. 8. 1880, p. 627), we have already had specimens of B. melanocephalus and B. rubicundus, and we have now for the first time an example of the perhaps still more curious B. calvus, which, according to Castlenau, is confined to the forests on the north bank of the Amazons, between the rivers Putumayo and Japura. The registered additions to the Society’s Menagerie during the month of July were 166 in number ; of these 82 were acquired by presentation, 44 by purchase, 33 by birth, and 6 were received on deposit. One young Pheasant, received during the month, was bred from some eggs laid in the Society’s Gardens and sent into the country to be hatched. The total number of departures during the same period by death and removals was 105. Among the additions may be specially noticed two rare American Parrots—a Lear’s Macaw (Ara leari) and a Lineolated Parrakeet (Bolborhynchus lineolatus), acquired by purchase. 1 See P. Z. 8. 1879, p. 551 Proc. Zoou. Soc.—1886, No. XXVIII. 28 418 DR. LUTKEN ON CHIROPODOMYS PENICILLATUS. [Noy. 16 The total number of registered additions to the Society’s Mena- gerie during the month of August was 98; of these 50 were acquired by presentation, 14 by purchase, 15 by birth, 6 were received on deposit, and 5 in exchange. Eight Elliot’s Pheasants, received during the month, were bred from some eggs laid in the Society’s Gardens and sent into the country to be hatched. The total number of departures during the same period by death and removals was 104. The total number of registered additions to the Society’s Mena- gerie during the month of September was 80; of these 42 were acquired by presentation, 4 by purchase, 2 by exchange, 19 were bred in the Gardens, and 13 were received on deposit. The total number of departures during the same period by death and removals was 84. The following are of special interest :— A Spot- ringed Snake (Liophis pecilogyrus) from Brazil, presented by Edgell Hunt, Esq., September 9th, new to the collection. Two Elegant Galidias (Galidia elegans) from Madagascar, pre- sented by Burt C. Miiller, Esq., September 16th. The total number of registered additions to the Society’s Mena- gerie during the month of October was 77, of which 11 were by birth, 45 by presentation, 5 by purchase, 6 by exchange, and 10 were received on deposit. The total number of departures during the same period by death and removals was 112. An extract was read from a letter addressed to the President by Dr. Emin Bey, dated Wadilai, Eastern Equatorial Africa, Jan. Ist, 1886. After speaking of the skull of a Chimpanzee and of some skins and skeletons of other Mammals and Birds obtained in Monbottu, which he proposed to send to the Society, Dr. Emin Bey continued as follows :-— “Tt may be interesting for you to hear that an anthropoid Ape exists in Uganda and Unyoro. I cannot say whether it is identical with the Monbottu Chimpanzee or not. While staying in these countries the negroes told me much about this animal, and in a MS. map which I forwarded to Dr. Petermann I fixed its northern limit at 2° N. lat. Now I hear that this Ape is frequent in the thick forests near Ugoma, and I hasten to beg my friend King Kabrega for some specimens.” A letter was read addressed to the Secretary by Dr. Chr. Liitken, of Copenhagen, F.M.Z.S. Referring to Mr. O. Thomas’s statement (P. Z.S. 1886, p. 78) that Chiropodomys penicillatus was a rare animal in Museums and that its distribuuon was not certainly known, Dr. Liitken announced tae i ee ee ee 1886.] PROF, FLOWER ON A SPECIMEN OF ARMADILLO. 419 that the Museum of Copenhagen had received in 1878 a specimen of this mammal in spirit from Buitenzorg, Java, forwarded by the late Mr. Kébke, Danish Consul at Batavia, and that he has been infermed by Mr. H. Winge that several specimens of it from the same locality were in the Museo Civico of Genoa. A letter was read from Dr. A. B. Meyer, C.M.Z.S., communi- cating the following remarks by Mr. K. G. Henke on a specimen of a hybrid Grouse, in the Dresden Museum, referred to by Dr. Collett in a previous communication :— * Dr. Collett has declared (supra, p. 225, note) a hybrid which I have figured, ‘ Zeitschrift fiir die gesammte Ornithologie,’ 1885, p- 47, pl. iii., ‘to be clearly only a partial albino of Tetrao tetrir fem.,’ but without giving his reasons for this opinion. “TJ will not discuss the question now, whether Zetrao tetrix or Lagopus albus was the father of this specimen, as it is treated and refigured, not as a single example of its kind, but together with others, similar and varying, in Dr. Meyer’s forthcoming work ‘ Unser Auer-,Birk- und Rackelwild,’ which will be illustrated by 15 coloured folio plates. I only wish to remark here, that Dr. Collett’s view of the said specimen does not appear to be correct, as supposing it really were a partial albino, a strong partial melanism would still be present, to account for the many black patches and markings, of which there is no trace in the female Tetrao tetrix —a coincidence which no one will admit, and which never has been observed. Besides, the albino of Tetrao tetriz, fem., has no such regular markings as the specimen in question. ‘IT therefore cannot agree with Dr. Collett, but am convinced that he is mistaken in declaring the Dresden specimen to be a partial albino.” Prof. Flower exhibited a specimen of an Armadillo, now belonging to the Museum of the Scarborough Philosophical Society, but the origin of which unfortunately appeared to be unknown. It was evi- dently a member of the genus Tatusia, and closely allied to the common T. novemeincta or T. peba, from which it differed mainly in having the whole of the carapace covered with a thick coating of light brown, fine, but rather stiff hair, about an inch and a half in length. The same kind of hair grew on the cheeks, the proximal portion of the limbs, and (though less abundantly and shorter) on the whole under surface of the body. The cephalic shield, the snout, the hands and feet, and the tail (except quite at the base) were bare. The covering of the hair of the back and sides was so thick as completely to conceal the carapace, except near the antero-inferior margin of the scapular region; but the usual scutes and bands were seen to be present on separating the hair, which only grew from the intervals between them. The length of the head was 33, of the body 84, and of the tail 83 inches. Unfortunately nearly the whole of the skull had been removed, but some of the anterior teeth which remained in the jaws were of very small size and appeared to indicate that the animal was young. 28* 420 MR. BLANFORD ON PARADOXURUS JERDONI. [Nov. 16, There was little doubt of the specific identity of the specimen with that belonging to the Vienna Museum, described by Fitzinger under the name of Cryptophractus pilosus*, and also with two specimens from Guyaquil in the Lima Museum, described and figured by Burmeister as Praopus hirsutus*, if, as was probably the case, the smaller size of the present specimen could be attributed to its not being full-grown. So far as Prof. Flower knew, these were the only published indications of the existence of this somewhat remarkable species, or at all events very distinct variety, of Armadillo, of which no specimen existed in our National collection. Prof. Bell exhibited and made remarks upon an object (apparently of the nature of an amulet) supposed to have been made from some portion of the skin of a mammal. It had been obtained from the natives at Moreton Bay, and sent to Kew, being supposed to be of vegetable origin. Mr. Seebohm exhibited a skin of the Lesser White-fronted Goose, Anser albifrons minutus (Anser erythropus, Linn. Syst. Nat. i. p- 197), which had been shot on the 16th of September last near Holy Island, on the coast of Northumberland, by Mr. Alfred Crawhall Chapman, of Sunderland. It was the first recorded example of the small form of the White-fronted Goose which had been obtained on the coasts of our islands, and it was especially interesting as being a young bird in first plumage. It proved to be a female on dissection, and bore a remarkable resemblance to the young in first plumage of the dark-bellied or typical form of the Brent Goose, Anser brenta ; but its much greater expanse of wing (4 feet) and its large legs and feet, which were yellow-ochre in colour when first shot, precluded the possibility of confounding it with that species. Its very small bill, quite as small as that of the Brent Goose, showed it to be a small example of the small form of the White-fronted Goose, but in so young a bird the white forehead had not yet appeared. Mr. W. T. Blanford exhibited a stuffed skin, the first perfect specimen he had seen, of Paradowxurus jerdoni, described and figured in the Society’s Proceedings for 1885 (pp. 613, 802, pl. xlix.). For this specimen, which was killed at Kateri (Kartary) on the Nilgiri hills, Mr. Blanford was indebted to Mr. G. F. Hampson, of Dun- sandle, Ootacamund, who had identified the species from the descrip- tion, and had confirmed the suggestion already made by Mr. Blanford, l.c. p. 618, that this species inhabits the Nilgiri hills as well as the Animalé range. The following papers were read :— 1 Tageblatt, Nr. 32; Versamml. deutsch. Naturf. u. Aerzte, 1856, Nr. 6, 8. 123. I am only acquainted with this reference through Fitzinger’s subsequent paper, “Die natiirliche Familie der Giirtelthiere (Dasypoder),” in Sitz. der k. Akad. der Wissensch., Band Ixiy, 1 Abth. (1871). ? Abhandl. naturf. Gesell. Halle, B. vi. p. 147 (1861). 1886.] COL. C. SWINHOE ON THE LEPIDOPTERA OF MHOW 421 1. On the Lepidoptera of Mhow, in Central India. By Colonel C. Swinuos, F.L.S., F.Z.S. [Received June 3, 1886.] (Plates XL. & XLI.) I collected Lepidoptera at Mhow from September 1881 until August 1882, with the assistance of a trained native, whose captures were daily recorded. My military. duties kept me well employed, and as I also collected birds and took notes on them during the whole of this period, the results of which have since appeared in ‘ The Ibis,’ I had not much time to give to the study of Lepidoptera ; and therefore this paper only professes to contain a list of Lepidoptera taken in Mhow and its immediate neighbourhood for a year, with the addition of a few taken by my subordinates at the sub-stations of Neemuch and Assirghur. I am indebted to Lord Walsingham for working out the specimens of Tortricidze and Tineina. Types of all the new species mentioned in this paper have been presented by me, as usual, to the British Museum. I. RHOPALOCERA. NyYyMPHALID& EuPL@IN&. 1. TrRUMALA LIMNIACE. Pap. limniace, Cramer, Pap. Exot. i. pl. 59. f. D, E (1775). Common from September to July. 2. SALATURA GENUTIA. Pap. genutia, Cramer, Pap. Exot. iii. pl. 206. f. C, D (1779). Common from September to July. 3. LiMNAS CHRYSIPPUS. Pap. chrysippus, Linn. Syst. Nat. p. 471 (1758). Common everywhere from September to Marci. 4, LIMNAS ALCIPPOIDES. Limnas alcippoides, Moore, P. Z. 8. 1883, p. 238, pl. 31. f. 1. I took one example of this variety at Mhow in June 1882, and one at Panghur near Neemuch in November 1884. 5. CRASTIA CORE. Pap. core, Cramer, Pap. Exot. iii. pl. 266. f. E, F (1780). March and June. Very plentiful in March ; only one example taken in June, 422 COL. C. SWINHOE ON THE [Nov. 16, SATYRINZE. 6., MELANITIS LEDA. Pap. leda, Linn. Syst. Nat. i. 2, p. 773 (1767). June, July ; September and October. 7. MELANITIS ISMENE. Pap. ismene, Cramer, Pap. Exot. i. pl. 26. f. A, B (1775). Common during the cold weather from the latter end of October to the beginning of March. I took, however, one example in June 1882. 8. CALYSISME PERSEUS. Pap. perseus, Fabr. Syst. Ent. p. 488 (1775). October and April. Only one example taken in the latter month ; it was fairly common in October 1881. 9. CALYSISME DRUSIA. Pap. drusia, Cramer, Pap. Exot. i. pl. 84. f. C, D (1779). I found one example of this variety of C. mineus, Linn., in a col- lection of Butterflies taken at Mhow in 1881 by Major Yerbury, R.A. It is smaller and paler than the types in the British Museum, but is otherwise identical. Cramer’s type came from China, but I have typical examples in my collection from the. Kangra valley and from Darjiling. 10. YpruHiIMA INICA. Ypthima inica, Hewitson, Trans. Ent. Soe. ser. 3, vol. ii. p. 285 (1865). Mhow, December; Depalpore, November. This is said to be an African insect, but the examples taken as_ above are identical with Hewitson’s type. 11. YpTHIMA ALKIBIE, N. sp. Upperside dark brown, with the ocelli as in Y. intca, but the general coloration is darker and brighter. Underside pale whitish brown, thickly covered with short delicate pale reddish-brown strige, which are uniformly disposed, but paler on the costa and margins of the fore wings in most specimens, and both wings with a marginal brown line and submarginal brown, slightly sinuated fascia ; the ocelli as in Y. inica, but one or other of the three minute ocelli on the hind wings is often more or less obsolete. Hind wings with three pale reddish-brown speckled zigzag bands, and can easily be distin- guished from Y. inica because the inner discal band curves outwardly, whereas in the type of Y inica this band curves inwards. Expanse of wings 1;4,—1%; inch. Mhow, November to March, very plentiful ; Depalpore, January and February. 1886. ] LEPIDOPTERA OF MHOW. 423 12. YpTHIMA MAHRATTA, Ypthima mahratta, Moore, Journ. As. Soc. Bengal, vol. liii. pt. 2, no. i. p. 1 (1884). Mhow, July and November; Neemuch, September to November. 13. YPTHIMA ALEMOLA. Ypthima alemola, Swinhoe, P. Z. 8. 1885, p. 127. April to July. 14. YeTHIMA DEDALEA, 0. sp. Allied to Y. ariaspa, Moore. Upperside dark brown, with the ocelli as in Y. inica, the one on the hind wing being minute, but with a clear ring of yellow round it. Underside pale grey, marginal lines brown ; both wings covered with short brown strigze, uniformly disposed, with a submarginal whitish fascia, bordered on the outer side by an incomplete brown, slightly zigzag line; pupils of the ocelli pale blue, metallic; fore wing with one subapical large ocellus, bi-pupilled: hind wing with three light distinct ocelli—one large (slightly smaller than the one on the fore wing), subapical, placed well inside the wing, almost in the disk, and with its upper part overlapping the second subcostal nervule; one a little smaller, in the interspace between the second and third median nervules ; and a third, the smallest, is duplex at the anal angle ; these ocelli are very curious: commencing with the largest one near the apex of the fore wings, they are gradually smaller, and the three first are in a perfectly straight line, the mimute duplex one at the anal angle being at an obtuse angle inwards; all the ocelli have broad uniform yellow rings with brown borders, and the duplicate ocellus at the anal angle is distinctly divided with yellow, but not cut between by the brown ring, which borders the outer yellow only, making it a complete duplex ocellus. Expanse of wings 1,2; inch. Mhovw, June 1882. 15. YPTHIMA RARA. Ypthima rara, Butler, P. Z. S. 1883, p. 145, pl. xxiv. f. 1, May to November, very plentiful; Neemuch, November. 16. YprHiMa COMPLEXIvA, n. sp. (Plate XL. fig. 2, 2.) Shape, colour, and markings above identical with Y. rara. The underside is, however, quite different, colour pale greyish, covered with dark chocolate-brown strigze, and with an indistinct incomplete submarginal zigzag line, more distinct in parts of the hind wings: fore wings with a large subapical ocellus, bi-pupilled, with a deep yellow ring, bordered with brown, pupils bright blue metallic, and with another smaller blind ocellus just below it, also with a yellow ring round it: hind wings with three black, very minute spots where the ocelli should be placed, as in FY. inica. Expanse of wings 1,5; inch. Depalpore, November. 424 COL. C. SWINHOE ON THE [Nov. 16, 17. LETHE NEELGHERRIENSIS. Satyrus (Cyllo) neelgherriensis, Guérin, Delessert’s Voy. dans Inde, pt. ii, p. 74, pl. 21. f. 1, 1 @ (1843). March, April, and May. ACREINZ. 18. TELCHINIA VIOLZ. Pap. viola, Fabr. Syst. Ent. p. 460 (1775). Mhow, September (Yerbury). NYMPHALIN&. 19. ATELLA PHALANTA. Pap. phalanta, Drury, Ill. Ex. Ent. i. pl. 21. f. 1, 2 (1773). Common, September to July. 20. PYRAMEIS CARDUI. Pap. cardui, Linn. Faun. Suec. p. 276 (1761). Common from September to December. 21. JUNONIA LEMONIAS. Pap. lemonias, Linn. Mus. Ulr. p. 277 (1764). Common from September to July. 228 JUNONIA HIERTE. Pap. hierte, Fabr. Ent. Syst. Suppl. p. 424 (1798). Common from September to July. 23. JUNONIA ORYTHIA. Pap. orythia, Linn. Mus. Ulr. p. 278 (1764). Common from September to July. 24. JUNONIA ASTERIE. Pap. asterie, Linn. Syst. Nat. i. 2, p. 769 (1767). Common from September to November. 25. JUNONIA ALMANA. Pap. almana, Linn. Mus. Ulr. p. 272 (1764). October, January, and March. 26. HyPpANIS POLINICE. Pap. polinice, Cram. Pap. Exot. iv. pl. 375. f. G, H (1782). October to December. 27. HypaANIs SIMPLEX. Hypanis simplex, Butler, P. Z. S. 1883, p. 146, pl. 24. f. 8. Mhow, June, July, and October; Depalpore, January ; Assir- ghur, September. 1886. ] LEPIDOPTERA OF MHOW. 42 or 28. HypoLIMNAS BOLINA. Pap. bolina, Linn. Mus. Ulr. p. 295 (1764). Mhow, July. Neemuch, November; Assirghur, October. 29. HypoLimMNas AVIA. Pap. avia, Fab. Ent. Syst. iii. 1, p. 111 (1793). Mhow, September and October ; Neemuch, September to Novem- ber, in great plenty. This is merely the large form of the preceding. 30. HyPoLIMNAS MISIPPUS. Pap. misippus, Linn. Mus. Ulr. p. 264 (1764). September to February. The females all mimic L. chrysippus. 31. NEPTIS EURYMENE. Neptis eurymene, Butler, P. Z. 8S. 1883, p. 145, pl. 24. f. 5. February to April. 32. SYMPHZEDRA NAIS. Pap. nais, Forst. Nov. Spec. Ins. p. 73 (1771). Pap. thyelia, Fabr. Ent. Syst. iii. 1, p. 142 (1793). Common from October to July. 33. CHARAXES FABIUS. Pap. fabius, Fabr. Spec. Ins. ii. p. 12 (1781). June and October. 34, CHARAXES AGRARIUS, n. sp. (Plate XL. fig. 3, 3.) Allied to C. athamus, Drury, and C. hamasta, Moore. Smaller than either ; nearest to the latter, but differs in having both wings with the discal transverse band one-fourth narrower in width, the subapical spot on the fore wing is small, whereas in C. Aamasta this spot is a lengthened square, and in the male there are two smaller upper apical spots. On the hind wing the submarginal white spots are prominent, but there is no outer marginal row of ochreous lunules. Expanse of wings 2 3,-2.5, inches. Mhow, October ; Assirghur, October. LYCHZNID2. 35. POLYOMMATUS B2ETICUS. Pap. beticus, Linn. Syst. Nat. ii. p. 789 (1766). September to February. 36. CATOCHRYSOPS STRABO. Hesperia strabo, Fabr. Ent. Syst. iii. 1, p. 287 (1793). Lyc. kandarpa, Horsf. Cat. Lep. E. I. C. vol. i. p. 82 (1829). Common from September to July. 426 COU. C. SWINHOE ON THE [Nov. 16, 37. CATOCHRYSOPS CNEJUS. Hesperia enejus, Faby. Ent. Syst. v. Suppl. p. 430 (1798). July to October. 38. CATOCHRYSOPS PATALA. Lycena patala, Kollar, Hiig. Kaschm. iv. 2, p. 418 (1848). October to February. Very plentiful in October. 39. CATOCHRYSOPS HAPALINA. Catochrysops hapalina, Butler, P. Z. S. 1883, p. 148, pl. 24. f 2.33; December and January. 40. CaTocHRYSOPS ELLA. Catochrysops ella, Butler, P. Z. S. 1881, p. 606. September to November. 41. JAMIDES BOCHUS. Pap. bochus, Cramer, Pap. Exot. iv. pl. 391. f. C, D (1782). September to November. 42. ZizERA MAHA. Lycena maha, Kollar, Hiig. Kaschm. iv. 2, p. 422 (1848). Mhow, April, May, and June; Manpore, June. 43. Z1ZERA CHANDALA. ( Polyommatus chandala, Moore, P.Z.S. 1865, p. 504, pl. 31. pe : November, February, April, and May. Mr. Moore, in P. Z. S. 1882, p. 245, has put this ’species as a synonym to the preceding one. This I think isamistake. He had, if I recollect rightly, only two examples, both males, in his collection. They were quite common at Mhow; and I found no difficulty in recognizing them, they are much paler blue than Z. maha. The females are the same colour as the males, instead of brown ‘like Z. maha, and the underside in both sexes has very faint spots onf{the hind wings, each spot having a whitish ring round it. 44, ZizERA KARSANDRA. Polyommatus karsandra, Moore, P. Z.S. 1865, p. 505, pl. 31. fanz October to May. This insect is very variable in colour; the type is brown. Irre- spective of sex, the colour varies from blue to dark brown. I have many examples from Quetta, Metazai, Sukkur, Karachi, the Punjaub, Central India, the Deccan, and also from Aden, of many shades of colour, quite impossible to separate. 1886. ] LEPIDOPTERA OF MHOW. 427 45. Z1zERA DICRETA. Zizera dicreta, Butler, P. Z. S. 1883, p. 150. October to May. 46. ZIzERA PYGMA. Lycena pygmea, Snellen, Tijd. voor Ent. xix. pl. 7. f. 3 (1876). September to December. 47. ZIzERA SANGRA. Polyommatus sangra, Moore, P. Z. 8. 1857, p. 772, pl. 41. f. 8. Lycena indica, Murray, Trans. Ent. Soc. 1874, p. 525. October to February. Varies much in size in different localities. I have four definite uniform sizes taken in four different parts of India ; some are slightly paler than others, but otherwise all are identical. The uniform manner in which almost all the different Indian species of Zizera are marked on the wings below is very curious. Z. pygme@a has markings peculiar to itself, but all the others mentioned in this paper have the spots below arranged in almost exactly the same manner, Z. sangra differing from the others merely in the abseuce of the spot inside the cell. 48. NACADUBA ARDATES. Lycena ardates, Moore, P. ZS. 1874, p. 574, pl. 67. f. 1. November. 49, EVERES PARRHASIUS. Hesperia parrhasius, Fabr. Ent. Syst. iii. 1, p. 289 (1793). February and March. 50. CHILADES PUTLI. Lycena putli, Kollar, Hiig. Kaschm. iv. 2, p. 422 (1848). September to December. 51. CHILADES VARUNANA. Polyommatus varunana, Moore, P. Z. 8. 1865, p. 772, pl. 41. 6. May, September, October, November, and December. 52. CHILADES LAIUS. Pap. laius, Cram. Pap. Exot. iv. pl. 319. f. D, E (1782). November and December. 53. TARUCUS PLINIUS. Hesperia plinius, Fabr. Ent. Syst. iii.1, p. 284 (1793). September to July. 54. TaRucus NARA. Lycena nara, Kollar, Hiig. Kaschm. iv. 2, p. 421 (1848). September to July. 4128 COL. C. SWINHOE ON THE [Nov. 16, 55. TARUCUS THEOPHRASTUS. Hesperia theophrastus, Fabr. Ent. Syst. iii. 1, p. 281 (1793). September to July. 56. AZANUS UBALDUS. Papilio ubaldus, Cramer, Pap. Exot. iv. pl. 390. f. L, M (1782). January, April, and May. 57. AZANUS ZENA. Lycena zena, Moore, P. Z. 8. 1865, p. 505, pl. 31. f. 9. September, October, and November. 58. APHNXUS ELIMA. Aphneus elima, Moore, Ann. & Mag. Nat. Hist. ser. 4, vol. xx. p. 51 (1877). March. 59. APHNZEUS ICTIS. Aphneus ictis, Hewitson, Ill. D. L. p. 61, pl. 25. f. 8, 9 (1865). November to July. 60. APHNZUS BRACTEATUS. Aphneus bracteatus, Butler, P. Z.S. 1883, p. 147, pl. 24. fe HOS. October to June. 61. APHN&ZUS ZSTIVUS, n. sp. (Plate XL. fig. 1.) Upperside pale reddish grey, with the bands on the underside showing faintly through the wings; marginal line brown, fringe silvery white: hind wings with two brown spots on the anal angle on a slightly reddish ground. Underside pale yellowish cream- colour, bands pale reddish brown with metallic marks: fore wings with two short bands before the middle which do not go below the cell ; a median band broken in the middle, followed by a costal spot like a figure of 8, followed by two more larger spots, one touching the costa and the other below it like a figure of 8 broken off in the middle ; then a submarginal and a marginal band, marginal line dark brown: hind wing with an inner median and discal band, and with a submarginal and marginal band like those on the fore wings ; marginal line brown, and some brown marks on the abdominal margin. All the bands on both wings are margined with dark brown on both sides, and have a peculiar zigzag appearance in con- sequence of the zigzag formation of their borders. Expanse of wings 154; inch. Mhovw, May. 62. VIRACHOLA ISOCRATES. Hesperia isocrates, Fabr. Ent. Syst. iii. 1, p. 266 (1793). February, April, and November. 1886. ] LEPIDOPTERA OF MHOW. 429 63. BasPpA MELAMPUS. Pap. melampus, Cram. Pap. Exot. iv. pl. 362. f. G, H (1782). September to June. 64. NrLasERA APELLA, n. sp. (Plate XL. fig. 4, ¢.) Allied to N. amantes, Hewitson. Upperside of a brighter and paler blue, but similar to A. amantes in the deep costal band on the fore wings of the male, which is absent in the female, and in the far deeper costal band of the hind wings and marginal band of both wings. The underside is, however, quite different, the ground-colour being of a uniform pale brownish grey with an ochreous tinge, this tinge showing quite distinctly on the brown portions of the fore wings, the costal portion and much of the hind wing being silvery grey. Fore wings with one small spot in the cell near the base, and a larger one also within the cell, a little forward of its centre, the upper portions of both touching the sub- costal vein ; another spot, square and larger at the end of the cell, and a smaller one below this in the angle of the first median inter- space, and below this is a spot elongated into a band running along the interspace for more than half its length below the first median branch, and half filling up that portion of the interno-median inter- space; there is also a discal row of six confluent spots from the costa, commencing with a small one and getting gradually larger and ending on the first median branch at the end of the band; all the spots brown, surrounded with yellowish white, the white borders being clearest round the two spots in the cell and the two outside it. Hind wing with four or five brown spots near the base, a central whirl of spots of the same colour, disconnected, and irregular like a zigzag band, a discal whorl of similar spots but paler, and the space on each side filled in with other bands of spots so pale as to be only here and therevisible. Marginsof both wings brown, diffused inwardly; a black spot at the anal angle, and a white silvery streak on the margin running from this spot to the first median branch, and clouded with dark brown atoms. Tails black, tips white. Expanse of wings 2,), inches. Mhow, March. 65. TasyuRIA JEHANA. Tajuria jehana, Moore, P. Z.S. 1883, p- 529, pl. 49. f. 7. September. PAPILIONIDG. PIERINZE. 66. TeriAs L&ETA. Terias leta, Boisduval, Sp. Gén. i. p. 174 (1836). September to July. The commonest Butterfly in Mhow. 430 COL. C. SWINHOE ON THE [Nov. 16, 67. TERIAS DRONA. Terias drona, Horsfield, Cat. Lep. E.I.C. p. 137, pl. 1. f. 13 (1829). September, October, and November. = 68. TERIAS VENATA. Terias venata, Moore, Cat. Lep. E.1.C. i. p. 65, pl. 2. f. 2 (1857). June, July, September, and October. 69. TERIAS RUBELLA. Terias rubella, Wall. Trans. Ent. Soc. ser. 3, vol. iv. p. 323 (1867). October to April. In great numbers. 70. TeRIAS HECABE. Pap. hecabe, Linn. Mus. Ulr. p. 249 (1764). February, July, and September. 71. TERIAS HECABEOIDES. Terias hecabeoides, Mén. Cat. Mus. Petr., Lép. i. p. 85, pl. 2. f. 2 (1855). September, October, and November. 72. TERIAS ZSIOPE. Terias esiope, Mén. Cat. Mus. Petr., Lép. i. p. 85, pl. 2. f. 3 (1835). October. 73. TERIAS EXCAVATA. Terias eacavata, Moore, P. Z.S. 1882, p. 252. September to December. Very plentiful in December. 74. TERIAS PURREEA. Terias purreea, Moore, P. Z.8. 1882, p. 252. November to May. 75. TERIAS ASPHODELUS. Terias asphodelus, Butler, P. Z. S. 1883, p. 151, pl. 24. £13 December to April. 76. TERIAS NARCISSUS. Terias narcissus, Butler, P. Z. 8. 1883, p. 151. December to February. 77. BELENOIS MESENTINA. Pap. mesentina, Cramer, Pap. Exot. iii. pl. 270. f. A, B (1782). Common all the year round. This is a very variable species ; some of the males are deep yellow 1886.] LEPIDOPTERA OF MHOW. 431 on the secondaries below, and many of both sexes vary much in the depth of the markings above, they also vary much in size. I have a female from Neemuch with the apical portion entirely black, and both males and females identical with and not separable from a pair in my collection taken by Major Yerbury in copuld at Haithalkim in Arabia, and identical with Walker’s type in the British Museum of B. lordaca from Damascus. Mr. Butler (P. Z. 8S. 1884, p. 492) says the males sent him by Major Yerbury from Huswah and Haithalkim are smaller than the Damascus type; but I have males both large and small from these localities, and a pair from the Punjaub quite as large as the Damascus insect, the male being a typical B. lordaca and the female only slightly paler in its marginal black borders. 78. HupHINA PHRYNE. Papilio phryne, Fabr. Syst. Ent. p. 473 (1775). September, October, and November. 79. HuPHINA ZEUXIPPE. Pap. zeuxippe, Cram. Pap. Exot. iv. pl. 362. f. E, F (1782). April, May, and June. 80. HupHINA CASSIDA. Pap. Danaus cassida, Faby. Ent. Syst. Suppl. p. 427. n. 595, 596 (1798). November to May. 81. GANORIS RAP. Papilio rape, Linn. Faun. Suec. p. 270 (1761). I took a worn female of this species in a garden at Mhow on the 6th of June, 1882, which I have still in my collection ; it is out of place in this list, but as I took it there myself I record it; its chrysalis might have come from England with somebody’s baggage. 82. APPIAS LIBYTHEA. Pap. libythea, Fabr. Syst. Ent. p. 471 (1775). June. 83. APPIAS ARES. Appias ares, Swinhoe, P. Z. 8. 1885, p. 138. January. 84. Deias EUCHARIS. Pap. eucharis, Drury, Il. Exot. Ent. ii. pl. 10. f. 5, 6 (1773). Common from September to July. 85. NEPHERONIA GAEA. Nepheronia gaea, Felder, Reise Nov., Lep. ii. p. 130 (1865). February and April. . 432 COL. C. SWINHOE ON THE Nov. 16, 86. CATOPSILIA PYRANTHEs Pap. pyranthe, Linn. Mus. Ulr. p. 245 (1764). Common all the year round. 87. CATOPSILIA PHILIPPINA. Pap. philippina, Cram. Pap. Exot. iv. pl. 361. f. C, D (1782). September to April. 88. CATOPSILIA CROCALE. Pap. crocale, Cram. Pap. Exot. i. pl. 55. f. C, D (1779). July. 89. CATOPSILIA CATILLA. Pap. catilla, Cram. Pap. Exot. iii. pl. 229. f. D, E (1782). Common from September to April. 90, IxIAS MERIDIONALIS. Ivias meridionalis, Swinhoe, P. Z. 8. 1885, p. 140, pl..9. f. 5, 2. May to August. 91. IxIAS DEPALPURA. Ivias depalpura, Butler, P.Z.S. 1883, p. 153, pl. 24. f. 6, 7. Depalpore lakes, November, December, and January. 92. Ix1As KAUSALA. Iwvias kausala, Moore, Aun. & Mag. Nat. Hist. ser. 4, vol. xx. p- 49 (1877). Depalpore lakes, November, December, and January. Very plentiful. All the females taken were albinos; the type female in Mr. Moore’s collection is primrose-coloured, and I have a primrose female taken with a male (identical with Mr. Moore’s type) in the Western Jumna canal. 93. TERACOLUS PERNOTATUS. Teracolus pernotatus, Butler, P. Z.S. 1876, p. 159, pl. 7. f. 1. Mhow, September ; Neemuch, September. 94. TERACOLUS BIMBURA. Teracolus bimbura, Butler, P. Z. 8. 1876, p. 161, pl. 7. f. 3, 4. January. This Zeracolus (which was originally named from specimens taken at Bimbur in Cashmir) is the most widely spread of all the genus. I have it from many parts of India, PAPILIONINE. 95. OpHEIDES ERITHONIUS. Pap. erithonius, Cram. Pap. Exot. iii. pl. 232. f. A, B (1782). Common from September to March. 1886.] LEPIDOPTERA OF MHOW. 433 96. LArRTIAS PAMMON. Pap. pammon, Linn. Mus. Ulr. p. 189 (1764). 2. Pap. polytes, Linn. Mus. Ulr. p. 186 (1764). Common from September to March. The females taken were all of M. diphilus form. 97. MENELAIDES DIPHILUS. Pap. diphilus, Esper, Ausl. Schmett. pl. 40 B. f. 1 (1785-98). Common from September to March. HESPERIDS&. 98. Pyreus GALBA. Hesperia galba, Fabr. Ent. Syst. iii. 1, p. 352 (1793). July, October, and December. 99. PLESIONEURA INDRANI. Plesioneura indrani, Moore, P. Z. 8. 1865, p. 789. September. 100. TexicoTa avuGtas. Pap. augias, Linn. Syst. Nat. i. 2, p. 794 (1767). Common from September to July. 101. PADRAONA MSA. Pamphila mesa, Moore, P. Z. S. 1865, p- 509, pl. 30. f. 9. February to May. 102. PARNARA BEVANI. Hesperia bevani, Moore, P. Z. 8. 1878, p. 688. July. 103. CHAPRA AGNA. Hesperia agna, Moore, P. Z.S. 1865, p- 791. July. 104. CHapra MATHIAs. Hesperia mathias, Fabr. Ent. Syst. Suppl. p. 433 (1798). December to April. 105. Suastus GREMIUS. Hesperia gremius, Faby., Butler, Cat. Fabr. Lep. B. M. p. 271 Boul. fy 2 « Hesperia divodasa, Moore, Cat. Lep. Mus. E.I. C. i. p. 255. Mhow, May, November, and December, scarce ; Depalpore, January, one taken ; Neemuch, September to November, common. ’ 106. IsoTEINON NILGIRIANA. Lsoteinon nilgiriana, Moore, P. Z. 8. 1883, p. 533. March. Proc. Zoo. Soc.—1886, No. XXIX. 29 434 COL. C. SWINHOE ON THE [Nov. 16, 107. TARACTOCERA SAGARA. Pamphila sagara, Moore, P. Z. 8. 1865, p. 792. April to July. 108. IsmENE ALEXIS. Papilio alexis, Fabr. Syst. Ent. p. 533 (1775). July. 109. BADAMIA EXCLAMATIONIS. Pap. exclamationis, Fabr. Syst. Ent. p. 530 (1775). Q. Pap. ladon, Cramer, Pap. Exot. iii. pl. 284. f. C (1782). June and July. II. HETEROCERA. SPHINGID&. 1. CEPHONODES HYLAS. Sphinz hylas, Linn. Mantissa, i. p. 539 (1771). September and December. 2. MACROGLOSSA GYRANS. Macroglossa gyrans, Walker, Cat. Lep. Het. viti. 91 (1856). July, September, and November. Common in September and in great plenty in November. 3. MACROGLOSSA BELIS. Sphinx belis, Cram. Pap. Exot. i. p. 147, pl. 94. f. C (1779). June, September, and November. In great plenty in November. 4, LopHuRA HYAS. Lophura hyas, Walker, viii. 107 (1856). November. 5. CH#ROCAMPA ALECTO. Sphine alecto, Linn. Mus. Lud. Ulr. p. 357 (1764). March and September. 6. CH#ROCAMPA THYELIA. Sphing thyelia, Linn. Mus. Lud. Ulr. p. 360 (1764). Common from September to November. 7. CHHZROCAMPA CELERIO. Sphinz celerio, Linn. Syst. Nat. i. 2, p. 800 (1766). Common from September to December. 8. CH&HROCAMPA OLDENLANDIZ. Sphina oldenlandie, Fabry. Sp. Ins. ii. p. 148 (1781). July and September. 1886.] LEPIDOPTERA OF MHOW. 435 9. DeILEPHILA LIVORNICA. Sphinx livornica, Esper, Ausl. Schmett. ii. pp. 87, 196, pl. 8. f. 4 (1785). June. 10. DAPHNIS NERII. Sphinz nerii, Linn. Syst. Nat. i. 2, p. 798 (1766). September, October, and November. 11. PotypTicHUs DENTATUS. Sphinx dentata, Cram. Pap. Exot. ii. p. 42, pl. 125. f. G (1779). October. 12. LrvcoPHLEBIA BICOLOR. Leucophlebia bicolor, Butler, P. Z. S. 1875, p. 16, pl. 2. f. 5. June and July. 13. BASIANA CERVINA. Basiana cervina, Walker, viii. 237 (1856). August (Forsayeth). 14. ACHERONTIA STYX. Acherontia styx, Westwood, Cab. Orient. Ent. p. 88, pl. 42. f. 3 (1847). September. 15. ACHERONTIA MORTA. Acherontia morta, Hiibner, Verz. bek. Schmett. p. 140 (1816). February and September. 16. PROTOPARCE ORIENTALIS. Protoparce orientalis, Butler, Tr. Z.S. 1877, vol. ix. part 10, p- 609. June, July, and September. 17. NEPHELE HESPERA. Sphinx hespera, Fabr. Syst. Ent. p. 546 (1775). Common from September to June. Very plentiful in November. Hawk-Moths were in extraordinary abundance in September 1881 in Mhow. A large thorny tree in my garden remained in full blossom for the greater part of that month, and I spent many evenings sitting under it watching these moths. About half an hour before sunset a few Cephonodes hylas would come, to be followed in a short time by Macroglossa belis and M. gyrans; then would fly by with a rush a single Nephele hespera. He would circle round and fly away, and a minute afterwards thousands of these insects would take possession of the tree. The solitary one always came first, apparently to see that all was safe, then flew away and a multitude of 29 436 COL. C. SWINHOE ON THE [Nov. 16, them would come, and the Macroglossa aud Cephonodes would dis- appear. In about half an hour the Nephele would vanish as suddenly as they came, just about the time it was getting dark; and from then till nine or ten o’clock Cherocampa thyelia, C. celerio, Daphnis nerii, and Protoparce orientalis would be hovering about the flowers, and by ten o’clock the tree would be deserted, and it would remain deserted until just before daybreak, when it always again had a crowd of visitors. They invariably came and went in the same order. I never found any on the tree during the middle of the night. SYNTOMIDZ. 18. ErEssA CONFINIS. Syntomis confinis, Walker, vii. 1592 (1856). April and October. I never saw this insect on the wing; I usually found them lying dead in the early morning in the verandah of my house. 19. SYNTOMIS CYSSEA. Sphinz cysseus, Cramer, Pap. Exot. iv. 124, pl. 355. f. B. January to March ; June, September, and November. Flying in swarms over the flowering poppy-fields in February. AGARISTIDZ. 20. EUSEMIA AFFLICTA. Eusemia afflicta, Butler, Ent. M. M. xii. p. 118 (1875). June. LiTHOSIID2. 21. ARGINA CRIBRARIA. Argina cribraria, Clerck, Icones, pl. 54. f. 4. September and October. 22. ARGINA NOTATA. Argina notata, Butler, Traus. Ent. Soc. 1877, part iv. Dec. p. 365. n. 270. September. 23. ARGINA ASTREA, Phalena astrea, Drury, Ill. Exot. Ins. ii, pl. vi. f. 3. September, October, and November. 24. DEIOPEIA PULCHELLA. Tinea pulchella, Linn. Syst. Nat. i. 2, p. 884. no. 349. September to March. 25. DEIOPEIA LOTRIX. Phalena lotriz, Cramer, Pap. Exot. ii. 20, pl. 109. f. E. September to March. 1886. ] LEPIDOPTERA OF MHOW. 437 26. AUMENE TENEBROSA. Aimene tenebrosa, Moore, P. Z. 8. 1878, p. 34. May and June. 27. LACIDES FICUS. Noctua ficus, Fabr. Ent. Syst. iii. p. 27. no. 62. September and October. ARCTIID. 28. ALOPE RICINI. Bombyx ricini, Fabr. Ent. Syst. ili. 1, p. 473 (1793). Alope ocellifera, Walker, iii. 620 (1856). August (Forsayeth). 29. CREATONOTUS INTERRUPTUS. Phalena interrupta, Linn. Syst. Nat. Phal. 116. September. 30. MicrosSEMYRA PALLIDA. Microsemyra pallida, Butler, P. Z. S. 1883, p. 155. October. 31. ALOA PUNCTISTRIGA. Spilosoma punctistriga, Walker, iii. 676 (1855). June and September. 32. ALOA EMITTENS. Creatonotus emittens, Walker, iii. 638 (1855). June. 33. ALOA SANGUINOLENTA. Bombyx sanguinolenta, Fabr. Ent. Syst. iii, 1, p. 473 (1793). September (Forsayeth). LipaRID&. 34, PERINA BASALIS. Perina basalis, Walker, iv. 966 (1855). September and October. 35. CHARNIDAS TESTACEA. Cycnia testacea, Waker, iii. 683 (1855). October, December, and March. 36. EuUpROCTIS LUNATA. Euproctis lunata, Walker, iv. 837 (1855). September. Both sexes vary much in colour from deep chrome-yellow to pure creamy white. 438 COL. C. SWINHOE ON THE [Nov. 16, 37. PoRTHESIA MARGINALIS. Euproctis marginalis, Walker, vii. 1731 (1865). June, September, and November. 38. ENOME DETERSA. Lymantria detersa, Walker, xxxii. 365 (1865). September to February. 39. ENOME INCERTA. Lymantria incerta, Walker, iv. 880 (1855). September, December, and February. 40. LyMANTRIA OBSOLETA. Lymantria obsoleta, Walker, iv. 880 (1855). September, November, December, and April. 41. OLENE FUSIFORMIS. Nioda fusiformis, Walker, v. 1070 (1855). September (Forsayeth). 42, PsALIs SECURIS. Psalis securis, Hiibner, Samml. exot. Schmett. iii. 9, 146. f. 291, 292. August (Forsayeth). 43, CHILENA STRIGULA. Lasiocampa strigula, Walker, xxxii. 563 (1865). September (Forsayeth). NotToDONTID2. 44, CETOLA DENTATA. Cetola dentata, Walker, v. 1016 (1855). July and September. 45. ANTHEUA DISCALIS. Antheua discalis, Walker, iti. 767 (1855). Mhow (Yerbdury). 46. BrreTa GALBANA, n. sp. (Plate XL. fig. 5.) 3 2. Thorax, fore wings, and antenne yellowish cream-colour ; head reddish brown, a stripe of the same colour down the centre of the thorax. Fore wingssparsely irrorated with black atoms, except in the centre, where they cluster together, forming a slight shade ; three rows of black dots—first just before the middle, consisting of two dots, one on the median vein, and the other close to the hinder margin ; the second discal, one on each nervule; the third marginal, minute but very distinct, one on the extremity of each nervule. Hind wings and abdomen pure white; underside pure white. 1886. ] LEPIDOPTERA OF MHOW. 439 an spots on the female are generally smaller than those on the male. Expanse of wings 15%, inch. June and July. 47. DaBaRITA ICTERICA, n. sp. (Plate XL. fig. 8.) Head, thorax, antenne, and fore wings pale reddish yellow, top of head and collar whitish ; fore wings with two outwardly oblique, thin, yellowish, slightly sinuous lines, rather close together, the first just before the middle, the second beyond the middle; the basal half of the wing the darkest, caused by numerous latitudinal brick-dust coloured minute regular lines or strigule, diffuse and terminating between the two lines. Abdomen pale dirty straw-colour ; hind wings white, semidiaphanous ; underside white, shining. Expanse of wings 1,4, inch. June. 48. IcHTHYURA RESTITURA. Ichthyura restitura, Walker, xxxii. 433 (1865). October. 49. OR#SIA EMARGINATA. Noctua emarginata, Fabr. Ent. Syst. ii. 2, p. 240. October. : LIMACODID. 50. MirEsA ALBIPUNCTA. Nyssia albipuncta, Herr.-Schiff. Lep. Exot. Sp. Ser. i. f. 179. October. 51. CANDYBA PUNCTATA. Candyba punctata, Walker, vii. 1761 (1856). Belgorea subnotata, Walker, xxxii. 497 (1865). June. Walker’s type of C. punctata is said to have come from Central Brazil, but the types of the above two species are identical. 52. NATADA BASALIS. Natada basalis, Walker, v. 1110 (1855). June and July. 53, PARASA LEPIDA. Phalena-Noctua lepida, Cram. Pap. Exot. ii. p. 50, pl. 130. f. E (1779). September. 54. APHENDALA TRIPARTITA. Aphendala tripartita, Moore, Trans. Ent. Soc. 1884, p. 376. June and July. 440 COL. C. SWINHOE ON THE [Nov. 16, 55. Susica CosMIANA, n. sp. (Plate XL. fig. 9, 92.) Allied to S. fraterna, Moore. pale reddish ochreous; 2 grey- ish ochreous, covered with silvery minute speckles, with the head and collar whitish. o¢ 2 with a minute spot at end of cell, more than two thirds of the wing from the base suffused with reddish, bounded by a reddish line curving outwardly from the costa near the apex, stopping short before the outer third of the hinder margin. Hind wings paler, reddish grey in the ¢, greyish ochreous in the 9. Underside in both sexes pale shining reddish ochreous. Expanse of wings ;%; inch. October to February. BomBycipD&. 56. TRILOCHA VARIANS. Naprepa varians, Walker, v. 1153 (1855). October and December. LASIOCAMPIDZ. 57. TARAGAMA GANESA. 3. Bombyx ganesa, Lefebvre, Zool. Journ. iii. p. 211 (1827). @. Bombyw siva, Lefebvre, /. c. p. 210. August (Yerbury). 58. TRISULA VARIEGATA. Trisula variegata, Moore, Cat. Lep. E.I. C. ii. p.420jpl. 12 a. f. 1 (1858-9). September. 59. TRABALA VISHNU. 2. Gastropacha vishnu, Lefebvre, Zool. Journ. iii. p. 207 (1827). 3. Amydona prasina, Walker, vi. 1417 (1855). September (Forsayeth). 60. LeBeDA BUDDHA. 3. Bombyx buddha, Lefebvre, Zool. Journ. ii. p. 209 (1827). 2. Bombyx brahma, Lefebvre, l. ¢. p. 208. August (Forsayeth). 61. EuprerOTE IGNAVUS, n.sp. (Plate XLI. fig. 1,3.) Allied to H. mutans, Walker. Male of a soft yellowish-fawn colour, the internal bands being much more deeply bent inwards towards the costa than in 2. mutans ; the insect is also much smaller and of altogether a different colour ; the bands on the hind wings are very distinct and, except at the base, are identical with those on the fore wings, which is not the case with #. mutans. Antennee, head, thorax, and all the bands and markings rufous-brown ; marginal border of both wings outside the outer double straight band much paler than the rest of the wings. 1886.] LEPIDOPTERA OF MHOW. 441 Basal third of the hind wings clothed with long pale hairs. Under- side clear greyish yellow, with the bands and marks as above but paler. Female of a uniform rufous-brown, coloured somewhat similarly to ¢ E. undata, Blanchard. Bands dark rufous-brown, placed as in the male but much straighter, less toothed and hardly at all bent in towards the costa, and the brown spots outside the outer straight band of the fore wings are wanting in the female; antenne, head, and body dark rufous-brown. Underside pale rufous ; markings as above but much paler. Expanse of wings, 63,5, 2 4 inches. June. DREPANULIDZ. 62. ARGYRIS EXTRUSATA. Ephyra extrusata, Walker, xxii. 637 (1861). October. SATURNIID&. 63. ANTHERZA NEBULOSA. Anthered nebulosa, Hutton, Journ. As. Soc. Bengal, 1869, p. 16. Common in the jungles below Assirghur from August to October. Cossip&. 64. PHRAGMATACIA MINOR. Phragmatecia minor, Moore, Desc. Lep. Col. Atkinson, part i. p- 87. June. 65. BRACHYLIA ACRONYCTOIDES. . Brachylia acronyctoides, Moore, P. Z. 8. 1879, p. 411, pl. 34. f. 4. June. NocrTueEs. LEUCANID&. 66. LEUCANIA EXTRANEA. Leucania extranea, Guénée, Noct. i. 77, 104. April. 67. LEUCANIA AUREOLA. Leucania aureola, Walker, ix. 108. September, in great numbers for about a fortnight. 68. LeucANIA INFERENS. Leucania inferens, Walker, ix. 105. Mr. Butler identified some Moths I sent him in 1882, taken in September 1881, as this species. 1 therefore enter it in this list, but I have no Mhow examples in my collection now, neither have I any note in my diary of Lepidoptera of having taken this insect in Mhow. 4492 COL. C. SWINHOE ON THE [Nov. 16, 69. LeucaNnta Byssina,n, sp. (Plate XL. fig. 6.) Antenne, head, thorax, and fore wings pale greyish white, very slightly tinged with ochreous. Fore wings shining, irrorated with black atoms, a black spot at the end of the cell, another before the middle in the interno-median area, a discal row of black points curving outwardly, deeply bent in towards the costa, and a marginal row of black points. Fringe long, same colour as the wing. Abdomen, hind wings above, and the entire surface below pure shining white. Expanse of wings 1-14, inch, June. 70. AXYLIA FURTIVA. Axylia furtiva, Swinhoe, P. Z. 8. 1885, p. 448. September. HELIOTHIDZ. 71. ALARIA LANCEOLATA. Alaria lanceolata, Walker, xxxiii. 767. September. 72. PRADATTA BIVITTA. Leucania bivitta, Walker, ix. 108. September. The above two species were together in great numbers in September 1881 for about a week. 73. PRADATTA BEATRIX. (Plate XLI. fig. 5.) Pradatta beatriz, Moore, P. Z. 8. 1881, p. 365. Antenne, head, thorax, and fore wings bright rosy pink. Fore wings with a cream-coloured stripe from base to outer margin, passing through the whole length of the cell. Abdomen and hind wings silvery white, the latter in some specimens stained here and there with rosy. Underside silvery white, brownish towards the basal centre of the fore wings, and stained with rosy grey here and there on both wings. Expanse of wings 1 inch. September. 74. HELIOTHIS ARMIGERA. Noctua armigera, Hiibner, Noct. pl. 79. f. 370. October, November, and December. 75. HeLioTHIs RUBESCENS. Thalpophila rubescens, Walker, xv. 1681. December. 76. HELIOTHIS PELTIGERA. Noctua peltigera, Wien. Verz. 89. 2. June and December. 1886. ] LEPIDOPTERA OF MHOW. 443 77. HELIOTHIS SUCCINEA. Heliothis succinea, Moore, P. Z. 8S. 1881, p. 362. November. 78. ADISURA LEUCANOIDES. Adisura leucanoides, Moore, P. Z. 8. 1881, p. 368. October. 79. ANTHAEXCIA SWINHOEI. Anthecia swinhoei, Butler, P. Z.S. 1883, p. 162. Assirghur, October. GLOTTULID. 80. GLOTTULA DOMINICA. Phalena-Noctua dominica, Cram. Pap. Exot. iv. p. 238, pl. 399. iH: August (Forsayeth). CyMATOPHORIDA. .81. RisoBa OBSTRUCTA. Risoba obstructa, Moore, P. Z. 8. 1881, p. 328. July. APAMIID&. 82. PRODENIA RETINA. Neuria retina, Frivaldsky, Herr.-Schiiff. Eur. Schmett. ii. 292, Noct. pl. 29. f. 145. October. 83. LAPHYGMA EXIGUA. Noctua exigua, Hiibner, Samml. Eur. Schmett., Noct. f. 362. February and March. 84. ILATTIA CEPHUSALIS. Ilattia cephusalis, Walker, xvi. 209. September and October. 85. MAMESTRA DOLOROSA. Mamestra dolorosa, Walker, xxxii. 667. October and November. 86. PrRIGIA SERVA. Celeena serva, Walker, xv. 1689. October. 87. PERIGIA CENTRALIS. Perigia centralis, Walker, xi. 734. June. 444 COL. C. SWINHOE ON THE [Nov. 16, NocrTuip. 88. AGROTIS SEGETUM. Phalena-Noctua segetum, Gmel. ed. Syst. Nat. i. 5, p. 2539. 1018. January to April. 89. AGROTIS SUFFUSA. Phalena-Noctua suffusa, Gmel. ed. Syst. Nat. i. 5, p. 2541. 1028. February. 90. AGROTIS ARISTIFERA. Agrotis aristifera, Guénée, Noct. i. 266, 426. April, June, November, and December. 91. AGROTIS LASSA, 0. Sp- Allied to 4. repulsa. Antenne, head, thorax, and fore wings dark brownish fawn-colour. Fore wings of the male very narrow ; fore wings of both sexes with some brown marks, like strigulee here and there ; on the male the usual stigmata are not visible; on the female the orbicular is represented by a black ring, and the claviform and reniform are both visible, but obscure and black ; and the latter is like a small smudged figure of 8. Hind wings white, semi- hyaline, with the costa and outer border tinged with fawn-colour. Abdomen grey, with the segments marked out with some white hairs. Underside paler, with the thorax, abdomen, and fore and hind wings streaked with silvery-white speckles. Expanse of wings 13 inch. March and April. HADENID&. 92. RADINACRA VARIANA, D. sp. (Plate XL. fig. 10.) _ Antennze, head, thorax, and fore wings brownish fawn-colour. Fore wings with the lines sinuous, dark brown, one subbasal extending only halfway down from the costa, another before the middle, and one submarginal ; all these complete and bending slightly outwardly ; three yellowish dots on the costa near the apex; the third line runs through the reniform stigma, which is hardly visible, the orbicular is indicated by a faint white spot. Abdomen greyish brown. Hind wings and underside pale brownish grey. Both wings above and below shining, almost gilded. Expanse of wings 1 inch. September. XYLOPHASIDA. 93. SPODOPTERA CILIUM. Spodoptera cilium, Guénée, Noct. i. 156. 249. March and October. 94, SPODOPTERA INFECTA. Prodenia infecta, Walker, ix. 196, October. 1886.] LEPIDOPTERA OF MHOW. 445 ERASTRIID HX. 95. LEPTOSIA QUINARIA, Leptosia quinaria, Moore, P. Z. 8. 1881, p. 371. April. ACONTIIDE. 96. ACONTIA SIGNIFERA. Acontia signifera, Walker, xii. 793. September. 97. ACONTIA NIGRIPALPIS. Acontia nigripalpis, Walker, xxxv. 1965. Assirghur, October. 98. ACONTIA BADIA, b. sp. Of a uniform pale reddish fawn-colour. Fore wing with whitish lines, thin, sinuous—one antemedian, one postmedian, one sub- marginal, and one marginal; a dark brown central band, stopping short of the costa, and expanding outwardly towards the apex, in some specimens overlapping the second line, in others having this line as its outer border for some distance upwards from the hinder margin ; the inner border of this band is upright, bent inwardly on the centre and well defined, and within this band is a deep black reniform mark, and another black mark beyond. Hind wings slightly darker towards the border, and rather more grey-coloured than the ground-colour of the fore wings. Underside: fore wings greyish brown, with the costa and hinder margin broadly pinkish yellow ; hind wings pale ochreous grey. Expanse of wings 38; inch. October. 99. ACONTIA CROCATA. Acontia crocata, Guénée, Noct. ii. 218, 989. October. 100. ACONTIA INDA. Acontia inda, Felder, Reise Nov. iv. pl. 108. fig. 23. June. 101. ACONTIA QUADRIPARTITA. Acontia quadripartita, Walker, xxxiii. 786. June. 102. ACONTIA EXCISA. Acontia excisa, Walker, MS., Swinhoe, P. Z. 8. 1885, p. 455. September. 103. PHOoTHEDES VEPRECULA. Phothedes veprecula, Swinhoe, P. Z. S. 1885, p. 456. June, September, and October. 446 COL. C. SWINHOE ON THE [Nov. 16, 104.. PHOTHEDES FRAUSA, N. Sp. Yellowish cream-colour. Fore wings diffused with pinkish, costa broadly grey; an indistinct silvery sinuous inner line, which in some specimens is disconnected and in some is wanting ; a similar out- ward line from the outer two thirds of the hinder margin up to the apex ; this line in many specimens runs in a brownish-grey shade, and there are streaks and marks of this colour on the costa, on the hinder margin towards the base, and marginal marks ; fringe also of same colour. Hind wings in some examples slightly grey towards the outer border, in others pure pale yellowish cream-colour, paler than the ground-colour of the fore wings. Underside of the same colour but paler, more whitish, shining, and quite unmarked. Expanse of wings 74; inch. July. Quite common for a few days. A somewhat variable-looking insect, because the colours and markings are much stronger in some than in others, the ground-colour in some females being almost pure pinkish. 105. HiccopA HERBARIA, 0. sp. Upperside, body, and wings white. Fore wings sparsely irrorated with reddish-brown dots and atoms, some marks of the same colour on the costa and outer margin, a sinuous line within a diffused band, from the outer two thirds of the hinder margin to the apex ; a square blackish large spot in the disk within this band; fringe white, marked with black marks. Hind wings with the outer half shaded with pale reddish brown ; fringe pure white. Underside whitish, shaded with grey, darkest on the costa. Palpi black, last joint very minute and pure white ; fore tarsi black with white bands. Expanse of wings ;§; inch. June and July. 106. TARACHE Nivosa, n. sp. (Plate XLI. fig. 14.) Head and thorax snow-white ; antenne and thorax reddish grey, the latter marked with pure white within the segmants, may be altogether white in freshly emerged specimens. Fore wings reddish slate-colour, in some specimens pale brown-pink, a deep snow-white band extending along four fifths of the costa, filling nearly the whole basal area with the dark colour of the wings, forming an elbow upwards in the centre part of the band; a reddish indistinct line crossing the band at the basal third, just before the elbow, a spot at the base within the band, also the orbicular and reniform spots all of the general colour of the wing, clear and distinct ; the dark part of the wing has white marks showing through here and there, and a brownish elbow parallel with the stigmata, giving the appearance of three spots in a longitudinal row ; marginal marks white; fringe white. Hind wings in some specimens white with greyish borders, in others of a uniform pale slaty grey ; fringe white. Underside pale grey, unmarked. 1886.] LEPIDOPTERA OF MHOW. 447 Expanse of wings 35, inch. June and September. A well-marked and pretty little insect. ANTHOPHILID. 107. THALPOCHARES ROSEANA. Thalpochares roseana, Moore, P. Z. 8. 1881, p. 370. April and May. 108. THALPOCHARES RIVULA. Thalpochares rivula, Moore, Desc. Lep. eol. Atkinson, ii. p. 140 (1882). March. 109. AGROPHILA SULPHURALIS. Phalena-Pyralis sulphuralis, Bergestr. Ins. Suec. 1. 16. October. 110. ANTHOPHILA INNUBILA, Nl. Sp. Upperside of a uniform shining cream-colour, the fore wings rather darker than the hind wings, and tinged with ochreous, especially on the costa. Fore wings sparsely covered with silvery- white freckles, and with a whitish line which extends upwards from the centre of the hinder margin towards the apex and then angles inwards, meeting the costa at the outer two thirds; there is also a faint indication of a similar inner line parallel to this just inside the middle. Eyes black ; antenne ochreous. Underside paler than the upperside, shining, unmarked. Expanse of wings 58; inch. June. 111. EuBLEMMA AMABILIS. Eublemma amabilis, Moore, Lep. Ceylon, iit. p. 54. June. PLusipa&. 112. PLustIa VERTICILLATA. Plusia verticillata, Guénée, Noct. ii. 344. 1168. September. 113. PLUSIA EXTRAHENS. Plusia extrahens, Walker, xii. 929. June and October. 114. Prusra c1IRCUMFLEXA. Phalena-Noctua circumflexa, Linn. Syst. Nat. 125. April. 448 COL. C. SWINHOE ON THE (Noy. 16, 115, PLusta ORICHALCEA. Noctua orichalcea, Fabr. Sp. Ins. ii. 227. 92. October (Forsayeth). HYBLAID&, 116. Hyspuaa PUERA. Phalena-Noctua puera, Cram. Pap. Exot. ii. 10, pl. 103. f. D, E. Mhow (Verdury). GONOPTERIDZ. 117. CosMOPHILA XANTHINDYMA. 3. Cosmophila wanthindyma, Boisd. Faun. Ent. Mad. Bourb. et Maur., Lép. p. 94, pl. 13. f. 7 (1833). Q . Cosmophila indica, Guénée, Noct. ii. 396. 1256 (1852). July, September, and October ; in great numbers in September. PoLYDESMIDZ. 118. PANDESMA QUENAVADI. Pandesma quenavadi, Guénée, Noct. ii. 438. 1310. May, July, and September. 119. PoLypESMA BOARMOIDES. Polydesma boarmoides, Guénée, Noct. ii. 441. 1314. June. 120. PotyDESMA BREVIPALPIS. Alamis brevipalpis, Waliser, xiii. 1051. June and July. 121. BAMRA ACRONYCTOIDES. Bamra acronyctoides, Moore, Desc. Lep. col. Atkinson, ii. p. 160 (1882). Mhow (Yerdury). HomortreRiD#. 122. HoMoPpTERA VETUSTA. Homoptera vetusta, Walker, xxxiii. 875. June, July, and October. 123. ALAMIS UMBRINA. Alamis umbrina, Guénée, Noct. iii. 4. 132. July and October. 124. ALAMIS CONTINUA. Alamis continua, Walker, xxxiii. 877. September (Forsayeth). 1886.] LEPIDOPTERA OF MHOW. 449 125. GrRPA FRATERNA. Girpa fraterna, Moore, Lep. Ceylon, iii. p. 94 (1884). September and October. 126. GrrPA INANGULATA. Hulodes inangulata, Guénée, Noct. iii. 210. 1612. Remigia optativa, Walker, xiv. 1510. Remigia optatura, Walker, xv. 1848. September and October. HypoGRAMMID&. 127. SELEPA CELTIS. Selepa celtis, Moore, Cat. Lep. E. I. C. ii. p. 353, pl. ix. a. f. 9. October (Forsayeth). 128. SELEPA OCCULTA. Selepa occulta, Swinhoe, P. Z. 8. 1885, p. 461. June. 129, SELEPA CURVIFERELLA. Subrita? curviferella, Walker, xxxv. 1745. September (Forsayeth). CaTEPHID. 130. EryGIA APICALIS. Erygia apicalis, Guénée, Noct. iii. 50. 1381. November. 131. BRIARDA BOLINOIDES. Briarda bolinoides, Walker, xv. 1802. July. 132. ANOPHIA OLIVESCENS. Anophia olivescens, Guénée, Noct. iii. 48. 1379. June. OMMATOPHORID. 133. PATULA MACROPS. Phalena-Noctua macrops, Linn. Syst. Nat. ii. 225. June and September. 134. ENroMOGRAMMA TORSA. Entomogramma torsa, Guénée, Noct. iii. 204. 1605. October. 135. Hom#A CLATHRUM. Homea clathrum, Walker, xiv. 1334. July. Proc. Zoou. Soc.—1886, No. XXX. 30 450 COL. C. SWINHOE ON THE [Nov. 16, Hypopryrip&. 136. SprIRAMIA HELICINA. Speiredonia helicina, Hiibner, Samml. exot. Schmett. iii. 14. 219. f, 437, 438. March, June, July, and September. OPHIDERID&. 137. ARGADESA MATERNA. Phalena-Noctua materna, Linn. Syst. Nat. ii. 840. 17. July. 138. OTHREIS FULLONICA. Phalena-Noctua fullonica, Linn. Syst. Nat. ii. 812. 16. July. OPHIUSID. 139. OpHIODES SEPARANS. Ophiodes separans, Walker, xiv. 1357. September (Forsayeth). 140. OpHIODES TRIPHENOIDES. Ophiodes triphenoides, Walker, xiv. 1358. Mhow (Yerbury). 141. SPHINGOMORPHA CHLOREA. Phalena chlorea, Cram. Pap. Exot. ii. p. 12, pl. 104. f. C. September and November. 142, ACH#HA MELICERTE. Phalena-Noctua melicerte, Drury, Ins. i. p. 46, pl. 23. f. 1. July to November. 143. ERCHEIA DIVERSIPENNIS. Ercheia diversipennis, Walker, xiii. 1108. September (Forsayeth). 144, OpHIUSA ALBIVITTA. Ophiusa albivitta, Guénée, Noct. ili. 271. 1707. July. 145. OpHrusA JOVIANA. Phalena-Noctua joviana, Cram. Pap. Exot. iv. p. 237, pl. 399. f. B Depalpore, November. 146. OOpHIUSA ARCTOTENIA. Ophiusa arctotenia, Guénée, Noct. iii. p- 272 (1852). Mhow ( Yerdury). 1886. ] LEPIDOPTERA OF MHOW. 451 147. GRAMMODES AMMONIA. Phalena ammonia, Cram. Pap. Exot. iii. p. 98, pl. 250. f. D. July and September. EvUcLipIIDz. 148. TRIGONODES HIPPASIA. ; ara hippasia, Cram. Pap. Exot. iii. p. 99, pl. 250. September, October, aud November. 149. ACANTHOLIPES AFFINIS. Docela affinis, Butler, Ann. & Mag. Nat. Hist. ser. 5, vol. v. p- 225 (1880). Mhow, October ; Assirghur, October. 150. ACANTHOLIPES ACERVALIS, 0. sp. 3. Cream-colour, sparsely irrorated with brown atoms ; head and collar pure white. Fore wings with a black dot in the cell and one or two in a line beyond it, a short grey longitudinal streak from the end of the cell to the outer border, some short grey streaks on the border, made by the interspaces near the border being nearly filled up with grey color, a black dot near the external angle (this is not present in all specimens); hinder margin grey. Hind wings ochreous grey towards the outer border. Underside white, fore wings suffused with purplish grey, darkest along the costa. Mhow, October. 1504. ANTHOPHILA PULCHRA, D. sp. Q. Allied to A. purpurina. Cream-colour; head and collar pure white. Fore wings with the costa and outer half suffused with purplish grey, gradually darkening towards the outer border, where there is a white streak running from the apex halfway down the outer margin, and then making a short streak inwards. Hind wings dark grey. Underside similar to the male, the purple on the fore wings rather darker. Expanse of wings 5%; inch. Mhow, November. REMIGIUDZ. 151. ReMIGIA FRUGALIS. Noctua frugalis, Fabr. Ent. Syst. iii. 2. 138. Common from July to December. 152. REMIGIA ARCHESIA. Phalena-Noctua archesia, Cram. Pap. Exot. iii. p. 145, pl. 273. f. F, G July, September, and October. PoAPHILIDA. 153. PoaAPHILA HAMIFERA. Poaphila hamifera, Walker, xxxiii. 992. July. 30* 452 COL. C. SWINHOE ON THE [Nov. 16, THERMESIIDZ. 154. AZAzIA RUBRICANS. Ophiusa rubricans, Boisd. Faun. Lép. Mad. p. 106. 11, pl. 16. f. 1. September. 155. MeEsTLETA BACCALIX, n. sp. (Plate XL. fig. 7.) Pale pinkish cream-colonr. Fore wings irrorated with pinkish- brown atoms; with four equidistant parallel whitish oblique lines— subbasal, antemedian, median, and postmedian ; each line nearly straight from hinder margin till near the costa, where it abruptly bends inwards to the costa; each line margined with pinkish brown on its inner side; outer border darker than the rest of the wing, with a whitish subapical line running inwards from the costa for a short distance ; fringe pinkish brown with white tips. Hind wings paler than the fore wings, pale pinkish brown towards the outer margin; fringe pinkish grey, with white tips. Underside whitish ; legs marked with pinkish brown ; body dark brown-pink ; fore wings suffused with pinkish brown towards the apex ; fringe of both wings as on the upperside. Expanse of wings 35, inch. December. Foci.uip2. 156. HinGuLa UNICOLORIS, 0. sp. Dark brown ; antenne articulated with white, tips of the palpi white ; head white on the inside of the eyes; wings saturated with pinkish ; fore wings with some black marks on the costa, a black streak at the end of the cell; both wings with black points on the outer margin, and with two irregular, very indistinct black lines across the wings difficult to distinguish. Underside slightly paler than the upperside, in one specimen quite unmarked, in another with faint traces of outer and submarginal lines. Expanse of wings 1 inch. February and September. PLaTYDID&. 157. EpispARIS SIGNATA. Episparis signata, Walker, xxxili. 1032. July. HyPENID&. 158. RaYNCHINA PERVULGALIS. s eR pervulgalis, Swinhoe, P. Z.S. 1885, p. 471, pl. 28. May and September. 159, RHYNCHINA XYLINA, 0. sp. Palpi, head, and collar white, speckled with grey, the palpi in 1886. ] LEPIDOPTERA OF MHOW. 453 some specimens mostly grey ; antenne grey, articulated with white, ciliated in the male, filiform in the female; thorax and fore wings dark grey speckled with white; an antemedian upright sinuous double white line, a median, outwardly oblique, sinuous double white line sharply bent inwards to the costa, round the reniform stigma, which is white and prominent; there is also an orbicular spot of the same colour, smaller and less prominent, some white marks on the costa near the apex, and a submarginal and a marginal brown line with white points. Hind wings and underside pale grey, unmarked ; abdomen grey with white segmental lines; male with a prominent grey anal tuft. This little insect varies much in the shade of its general coloration, some specimens being reddish grey, and in many the white pre- dominates. Expanse of wings ;3,—,5, inch. June and July ; common in the cotton-fields. 160. HypENA ABDUCALIS. Hypena abducalis, Walker, xvi. 67. Common in July. This species is very variable ; some are strongly marked like the type, others have merely a whitish curved line on the fore wings from the tip to the base, with a few streaks, and the general colour of the wing is pale and quite different to the type. HERMINIIDZ. 161. NopARIA EXTERNALIS. Nodaria externalis, Guénée, Delt. et Pyral. 64.78. October. 162. APPHADANA MISERA. Apphadana misera, Butler, P. Z. 8. 1883, p. 166. Mhow, October; Assirghur, October. 163. SPADIX VEGETUS. Spadix vegetus, Swinhoe, P. Z. S. 1885, p. 475, pl. 28. f. 14. June and September. 164. ByTURNA DIGRAMMA. Bocana digramma, Walker, xxxiv. 1170. September and October. 165. LABANDA PAMPHOSALIS. Bocana pamphosalis, Walker, xix. 887. October. 454 COL. C. SWINHOE ON THE [Nov. 16, GEOMETRITES. ENNOMIIDZ. 166. HypERYTHRA SWINHOEI. Hyperythra swinhoei, Butler, Ann. & Mag. Nat. Hist. ser. 5, vol. v. p. 223 (1880). Mhow, February ; Ajnot, November. 167. CHIZALA DECIPIENS. Chizala decipiens, Walker, xx. 263. March. BoaRMIID&. 168. HypocHROMA DISPENSATA. Hypochroma dispensata, Walker, xxi. 435. March. 169. BoARMIA CORNARIA. Boarmia cornaria, Guénée, Phal. i. 254. 390. February and October. 170. PETELIA MEDARDARIA. Petelia medardaria, Herr.-Schiff. Exot. Schm. pl. 94. f. 534. July. AMPHIDASID. 171. BuzuRa PANTERINARIA. Amphidasis panterinaria, Bremer und Grey, Beitr. zur Schmett.- Fauna des nérdlichen China’s, p. 21. 107. June. GEOMETRIDZ. 172. NEMORIA CARNIFRONS. Nemoria carnifrons, Butler, P. Z.S. 1883, p. 169. September and October. 173. NEMORIA FREQUENS. Nemoria frequens, Butler, P. Z. 8. 1881, p. 616. Mhow, March, April, and November ; Ajnot, November. 174. TIMANDRA DIATOMARIA. Timandra diatomaria, Walker, xxvi. 1616. September, October, and November. EpHyRIDaz. 175. EpHYRA CLEORARIA. Acidalia cleoraria, Walker, xxiii. 792. Mhow, February to June, also in October ; Depalpore, November and December. 1886. ] LEPIDOPTERA OF MHOW. 455 176. EpHyRA INEXACTA. Epione inexacta, Walker, xxvi. 1497. October. IDHIDZ. 177. Ip#A ADDICTARIA. Acidalia addictaria, Walker, xxii. 749. October. 178. ID#A PATULARIA. Acidalia patularia, Walker, xxxv. 1633. Delapore, November. 179. Ip#A REMOTATA. Acidalia remotata, Walker, xxii. 748. Depalpore, November. 180. Ip#A ABSCONDITARIA. Acidalia absconditaria, Walker, xxiii. 757. October, November, and December. 181. Ip#a WALKERI. Idea walkeri, Butler, P. Z.S. 1883, p. 170. Acidalia extimaria, Walker, xxiii. 794. October and January. 182. Ip#a NEGATARIA. Acidalia negataria, Walker, xxiii. 751. Mhow, December ; Depalpore, November. 183. Ipa#a CHOTARIA. Idea chotaria, Swinhoe, P. Z. 8. 1885, p. 858, pl. 57. f. 14. April and June. 184. Hyria BILINEATA. Hyria bilineata, Butler, P. Z.S. 1883, p. 170. Assirghur, October. CABERIDZ. 185. STEGANIA UVIDULA. Stegania uvidula, Swinhoe, P. Z.S. 1885, p. 860. July. MACARIID. 186. Macaria ELEONORA. Phalena eleonora, Cram. Pap. Exot. iii. p. 172, pl. 288. f. E, F, G. July. 456 COL. C. SWINHOE ON THE [Nov. 16, 187. MACARIA HEBESATA. Macaria hebesata, Walker, xxiii. 931. September. 188. MacaRiA ZEBRINA. Tephrina zebrina, Butler, P. Z.S, 1883, p. 171. March, April, and May. 189. MAcARIA ARENARIA. Tephrina arenaria, Swinhoe, P. Z.S. 1884, p. 527, pl. 48. f. 13. December. ‘ 190. MaAcaRIA LITHINA. Tiphrina lithina, Butler, P. Z.S. 1883, p. 171. March and October. I believe these to be females of M. zebrina, though at first sight they do not look like it, having no median bands; but I have never taken a male, and the female of the allied species, M. strenuata, Walker, is often also without bands and is hardly distinguishable from M, lithina. 191. MacarIA PEREMPTARIA. Macaria peremptaria, Walker, xxiii. 929. October. 192. MacarRiIA GRANITALIS. Tephrina granitalis, Butler, P. Z. 8. 1883, p. 171. September. FIpONIIDz. 193. STERRAA SACRARIA. : Phalena-Geometra sacraria, Linn. Syst. Nat. i. 2, p. 863. 220. February, May, and June. 194, STrERRHA PAULULA, n. sp. (Plate XLI. fig. 7.) White; eyes black; thorax and fore wings irrorated with ochreous atoms ; fore wings with a reddish-ochreous dot at the end of the cell, and with two obligue outer lines of the same colour close together, from the outer two thirds of the hinder margin, where they are separate, opening out in their centre and meeting at the apex; abdo- men and hind wings pure white. Underside white ; fore wings pale ochreous towards the costa. Expanse of wings 58; inch. May. LaRENTIID&. 195. LycAUGES DEMISSUS, N. Sp. Eyes black; top of head pure white; antennz, body, and wings cream-colour, both wings irrorated with brown atoms, which are 1886. | LEPIDOPTERA OF MHOW. 457 densely packed in places, forming bands along the costa and on all the borders of both wings. Fore wings with an oblique central band of the same colour (also irrorated with darker atoms) from the centre of the hinder margin to the apex; a row of brown dots between this band and the outer margin, the dots being connected together with a line of pale atoms; a brown dot at the end of the cell and sometimes one or two more in a row inwards; fringe white, densely irrorated with brown atoms, making it clearly interlined. Hind wings with a brown dot at the end of the cell, with a central band of the same colour as that in the fore wings, the band being curved inwardly to the costa; an outward row of dots connected together by brownish atoms, and a marginal row of dots; fringe as in fore wings ; in some specimens the outer line of atoms in both wings is double, with the dot on the inside line. Underside like the upperside, but darker and duller. Expanse of wings ;®; inch. February to June; common. 196. NapAGARA GRISEA. Nadagara grisea, Butler, P.Z. 8. 1883, p. 172. May. PYRALES, PyRALIDE. 197. PYRALIS LUCILLALIS. Pyralis lucillalis, Walker, xvii. 268. April and September. 198. PyRALIS UBERALIS. Pyralis uberalis, Swinhoe, P. Z. S. 1884, p. 523, pl. 48. f. 10. May. 199. CLEDEOBIA HYPOTIALIS. Cledeobia hypotialis, Swinhoe, P. Z.S. 1885, p. 866. June, September, and October ; in great plenty in June. ENNYCHIIDZ. 200. PyrausTA STULTALIS. Botys stultalis, Walker, xviii. 669. June and September. 201. RHODARIA JUNCTURALIS. Rhodaria juncturalis, Walker, xxxiv. 1283. September. ASOPIID, 202. HyMeEnNtIA FASCIALIS. cgi Alain fascialis, Cram, Pap. Exot. iv. p. 236, pl. 398. June, July, and September. 458 COL. C. SWINHOE ON THE [Nov. 16, 203. CoproBaSis OPISALIS. Desmia opisalis, Walker, xvii. 346. July and September. 204. CoproBASIS ZNEALIS. Coptobasis enealis, Swinhoe, P. Z. 8. 1885, p. 867. July. 205. SAMEA INSCITALIS. Aidiodes inscitalis, Walker, xxxiv. 1297. September. 206. LrvcINoDEs AUXIALIS, n. sp. (Plate XLI. fig. 12.) Head and thorax reddish brown, covered with white marks; abdo- men pure pearl-white, with pale reddish-brown bands in the jast four segments. Fore wings pure pearl-white, with a broad reddish-brown band at the base, and another on the outer border, diffused inwardly, and filling up the outer third of the wing ; a white line at the base, and another submarginal, both sinuous, and showing distinctly on the brown bands, which are also covered with white marks as on the thorax; there are also some pale reddish marks on the costa in the central portion of the wing. Hind wings white, semihyaline, with a discal waved line and an interrupted marginal band diffused inwardly ; both pale reddish brown; fringe of both wings white. Underside white, with the bands and marks pale, showing through the wings. Expanse of wings ;4,—;5, inch. April. HyDROCAMPIDZ. 207. PARAPONYX AFFINIALIS. Paraponyz affnialis, Guénée, Delt. et Pyral. 270. 259. October, November, January, March, April, and June; very plentiful. HERCYNIDE. 208. HerBuLa MELEAGRISALIS. Herbula meleagrisalis, Walker, xvii. 324. April. SPILOMELIDZ. 209. SALBIA PEKSPICUALIS. Zebronia perspicualis, Walker, xxxiv. 1347. October. 210. ZEBRONIA AUROLINEATUS. Zebronia aurolineatus, Walker, xvii. 478. Assirghur, October. 1886.] LEPIDOPTERA OF MHOW. 459 211. ZEBRONIA GRAPHICALIS, 0. Sp. Allied to Z. obrinusalis, Walker. Ochreous ; fore wings with a black dot at the end of the cell and three black dots on the costa—one basal, one before and another beyond the middle, exactly as in Z. aurolinealis and Z, plutusalis. Both fore and hind wings crossed by five dark ochreous, slightly sinuous bands; marginal line dark ochreous ; fringe long, with pale tips. Underside paler ; wings unmarked, except a deep black spot at the end of the cell of the fore wings ; all the legs with black knees ; fore tarsi with three black bands. Expanse of wings ;°,—1 inch. February, March, and July. MARGARODID&. 212. PyGosPILA TYRESALIS. Phalena-Pyralis tyres, Pap. Exot. iii. p. 124, pl. 263. f. C. Pygospila tyresalis, Guénée, Delt. et Pyral. 312. 340. Mhow (Yerbury). 213. PHAKELLURA INDICA. Eudioptis indica, Saunders, Zool. ix. 3070. September, October, and November. 214. GLYPHODES FESSALIS, n. sp. (Plate XLI. fig. 13.) Palpi unusually long, much longer than the breadth of the head ; antenn, palpi, head, thorax, and abdomen pure white ; a reddish band on each side of the collar, joining a similar band on the costa of the fore wings ; outer border of fore wings with a band of the same colour—in some specimens purplish, margined inwardly with a brown line. Hind wings white, semihyaline, with an outer border slightly paler than that on the fore wings, and which becomes gra- dually attenuated to the anal angle; fringe of both wings white. Underside white, shining, with the bands faintly showing through. Expanse of wings 35; inch. April and May. 215. EvcLasTa DEFAMATALIS. Tlurgia defamatalis, Walker, xviii. 544. November. BortipiDz. 216. Borys AUREA. Botys aurea, Butler, Ill. Typ. Lep. Het. iii. p. 76, pl. 59. f. 11 (1879). October. 217. Borys INCOLORALIS. Botys incoloralis, Guénée, Delt. et Pyral. 332. 369. October. 460 COL. C. SWINHOE ON THE [Nov. 16, 218. Borys OBSTRUSALIs. Botys obstrusalis, Walker, xviii. 663. July, September, October, and November. 219. Borys NEOCLESALIS. Botys neoclesalis, Walker, xviti. 635. June. 220. Borys MOLUSALIS. Botys molusalis, Walker, xix. 1409. August (Forsayeth). 221. EBULEA CATALAUNALIS. Botys catalaunalis, Duponchel, Lép. de France, viii. p. 330. pl. 232. f. 8. September, October, and November. 222. ScoPULA DAMASTESALIS. Scopula damastesalis, Walker, xix. 1013. July and September. 223. ScopULA VINCTALIS. Scopula vinctalis, Walker, xxxiv. 1476. July. 224. SCOPULA STRENUALIS. Botys strenualis, Walker, xxxiv. 1409. August (Forsayeth). STENIIDA. 225. DIASEMIA GEOMETRALIS. Lepyrodes geometralis, Guénée, Delt. et Pyral. 278. 271. Assirghur, October. PHYCIDE. 226. NEPHOPTERYX SUFFUSCALIS, 0. sp. Cinereous brown; whitish, shining, beneath; palpi stout, pubescent, curving upwards, not rising higher than the vertex, third joint lan- ceolate, short, not one third of the length of the second; antenne rather stout, brown marked with white ; top of head whitish ; palpi, thorax, and fore wings cinereous brown, some silvery-white atoms on thorax and on the fore wings near the base ; reniform stigma repre- sented by a whitish spot ; four sinuous incomplete black lines across the fore wings—basal, antemedian, postmedian, and submarginal ; marginal points black ; fringe long, greyish brown ; hind wings pale whitish cinereous. Expanse of wings 33; inch. March and April. 1886. ] LEPIDOPTERA OF MHOW. 461 227. Homa@mosoMA GRATELLA. Homeosoma gratella, Walker, xxvii. 26. February and April. CRAMBID. 228. SCH@NOBIUS BISIGNATUS. Schenobius bisignatus, Zeller, MS. (col. B.M.), P. Z.8. 1885, p- 878. June and July. 229. CHILO AURIFUSELLUS. Crambus aurifusellus, Walker, xxxv. 1756. June and July. 230. CHILO INTERRUPTELLUS. Chilo interruptellus, Moore, P. Z.S. 1872, p. 581, pl. 34. f. 5. June. 231. CHILO ORTELLUS, n. sp. (Plate XLI. fig. 3.) White ; palpi fawn-colour, porrect, about as long as the breadth of the head, second joiut with large white tufts above, third acutely conical, as long as the second ; antennze white, stout, pectinated in the male, branches reddish, short; top of head pure white; thorax grey, with a black central stripe and a white band on each side; abdomen pure white. Wings white; fore wings with the upper portions suffused with yellowish-fawn colour, and with a broad black longitudinal central stripe from base to outer margin, atten- uated at both ends; marginal points black, and a few black atoms distributed over the surface of the wing: hind wings pure white, unmarked. Underside white, with the stripe and marginal points on the fore wings showing through the wings, and in the male with the costal portions and outer border of the fore wings and costa of hind wings suffused with ey reddish grey. Expanse of wings, d 15%, 2 1;4 inch. June and July. 232. CHARLTONA KALA. Charltona kala, Swinhoe, P. Z.S. fabs s p. 879, pl. 57. f. 4, 3. June and July. 233. JARTHEZA CHRYSOGRAPHELLA. Chilo chrysographella, Kollar, Hiigel’s Kasch. p. 494 (1848). February to April, June and October. 234. JARTHEZA CASSIMELLA, bn. sp. (Plate XLI. fig. 4 g, fig. 6 2.) Allied to J. aylinella. Pale yellowish fawn-colour ; labial palpi porrect, stout, longer than 462 COL. C. SWINHOE ON THE [Nov. 16, the breadth of the head, last joint minute ; maxillary palpi half the length of the labial palpi. Antennze of the male pectinated, branches very short; of the female filiform, with short bristles, colour grey. Top of head and thorax chestnut-brown, latter with a white band on each side; abdomen grey, with white segmental lines. Fore wings yellowish fawn-colour, with two dark brown, diffuse, incomplete longitudinal stripes, one running a short distance out of the centre of the cell towards the outer border, the other from the base on the submedian vein for about two thirds of the length of the wing, each stripe containing a glistening silver-white streak ; a sub- marginal narrow semidentate brown band and black lunular small spots on the veins close to, but not touching, the outer margin ; fringe grey, with a brown line in its centre. Hind wings smoky grey, unmarked; fringe white. Underside whitish, shining; fore wings suffused with grey; legs fawn-colour, brown on their inner sides ; tarsi with brown bands. Expanse of wings, ¢ 13%, 2 17%5 inch. June and July ; common. 235. CRAMBUS PARTELLUS. Crambus partellus, Swinhoe, P. Z.8. 1885, p. 879. October. 236. CRAMBUS MULTIVAGELLUS, 0. sp. White ; antennz thin; labial palpi slender, as long as the breadth of the head ; maxillary palpi one third of the length of the labial palpi; abdomen extending a little beyond the hind wings; fore wings acute, rather narrow, outer border oblique, costa slightly convex ; wings and body above and below pure white, shining, un- marked. Expanse of wings 7%; inch. June, July, and September. 237. UROLA INCLARALIS. Crambus inclaralis, Walker, xxxvii. 166. June and July. 238. EROMENE BELLA. Eromene bella, Hiibner, Tin. f, 69. April and June. 239. SURATTHA INVECTALIS. Surattha invectalis, Walker, xxvii. 76. June. 240. Hypotia ALLALIs, n. sp. (Plate XLI. fig. 2.) White ; fore wings with the costal line and basal third very pale reddish cinereous, an oblique broad pale reddish-brown band beyond 1886. | LEPIDOPTERA OF MHOW. 463 the middle, on the inner margin of which is the reniform stigma, brownish, rather large, lunular; marginal line reddish brown, this line runs round the apex on to the costa and round the hinder angle a little way on the hinder margin; some faint, very pale, reddish marks on the outer third of the wing. Hind wings white, marginal line reddish brown ; fringe on both wings interlined—white, pale reddish brown, and white. Antenne, palpi, and body pure white; a thin brown band on the abdomen near the base, in some specimens like a fine line. Underside white, with the costal portion of the fore wings suffused with reddish. Expanse of wings ;/; inch. Mhow, June. NYCTEOLID&. 941. EARIAS FRONDOSANA. Earias frondosana, Walker, xxvii. 204. Assirghur, October. 242. EaARIAS TRISTRIGOSA. Earias tristrigosa, Butler, P. Z.S. 1881, p. 614. April. 243. EARIAS SPEIPLENA. Aphusia speiplena, Walker, xii. 770. October and December. TORTRICID. 244, PHyCoDES HIRUNDINICORNIS. Phycodes hirundinicornis, Guénée, Noct. ii. 389. 1249. Tegna hybleella, Walker, xxxv. 1810. April and September. 245. DicHRORAMPHA SUBSEQUANA. Tortrix subsequana, Haworth; Stephens ; Wood, figs 1021. June and October. TINEID. 246. ALAVONA BARBARELLA. Alavona barbarella, Walker, xxviii. 515. May and June, in great numbers. 247. ALAVONA COSSUSELLA. Alavona cossusella, Walker, xxxv. 1816. June and July, in great numbers in the former month. 464 COL. C. SWINHOE ON THE [Nov. 16, 248. ALAVONA INDECORELLA ? Alavona indecorella, Walker, xxvili. 515. June. Four male specimens, all more or less rubbed ; they are in size and appearance more like Walker’s type of the above than of any other insect in this genus, but they cannot safely be determined as iden- tical with this species. 249. ALAVONA MINOR, Walsingham, n. sp. (Plate XLI. figs. 10, 11, 3 2.) Palpi dull ochreous, shaded with brownish beneath ; head ochreous ; antennez cinereous; thorax brownish. Fore wings pale whitish fawn, shaded at the base of the costal margin with brownish, a series of brown spots around the apical and outer portions of the costal margins; between these and the end of the cell, in brightly marked specimens, is a second series of similar spots parallel to the apical margin, but turning outward to the anal angle at their lower end; a brownish spot is situated at the upper angle of the cell, another on the outer third of the fold. The markings in this species appear to be frequently almost obsolete, but the marginal spots are nearly always distinguishable. Hind wings slightly paler than the fore wings; abdomen tinged with brownish. Male, expanse 24 millim. The female has no markings, so far as can be judged froma single specimen in poor condition, but is much smaller than the female of Alavona cossusella, Walker. Female, expanse 26 millim. June and July, common. 250. TINEA SUBOCHRACEELLA, Walsingham, n.sp. (Plate XLI. fig. 9.) Head tufted, bright yellowish ochreous ; labial palpi ochreous, faintly tinged with greyish, short and drooping, not thickly clothed ; maxillary palpi as long as the labials. Fore wings shining ochreous, faintly tinged at the base of the costa and about the fringes and apex of the wings with purplish grey. Hind wings greyish ochreous, with a slight coppery tinge ; abdomen and legs pale ochreous. Expanse 13 millim. April. A single specimen, received from the Rev. J. H. Hocking, from Dharmsala, by Lord Walsingham, measures 15 millim. in the expanse of the fore wings. Two others of my Mhow specimens Lord Walsingham says are apparently not distinct from this species, although one of them is slightly larger in size (expanse 17 millim.), and is almost entirely devoid of the greyish tinge of the fore wings. The insect has much the appearance of Myrmecocela ochraceella, Tgstr., but differs in the form of the labial palpi. L’S. 1886. PL XL. 4 P. Hanhart imp IAN LEPIDOPTERA TAT TVT LIND P.Z.S. 1886.P1. XLT. W Purkiss lith NEW INDIAN LEPIDOPTERA . 1886.] LEPIDOPTERA OF MHOW. 251. HapsIFERA DEVIELLA. Drosica deviella, Walker, xxviii. 520. January, June, and July. 252. SETOMORPHA TINEOIDEs, Walsingham, n. sp. fig. 8.) Palpi pale greyish above, tinged with fuscous beneath; antennse greyish fuscous ; thorax and fore wings spotted and mottled with ill- defined patches of brownish fuscous scales, these are very numerous across the middle of the wing and form a series of spots around the costal, apical, and a portion of dorsal margins. with a faint purplish tinge ; abdomen greyish fuscous. Expanse of wings 14 millim. April, May, and June. CRYPTOLECHIIDA. 253. DEPRESSARIA SWINHOEI. Depressaria swinhoei, Butler, P. Z.S. 1883, p. 174. October. cS 0a mt SOMAID OB Oboe za oe SONIDO Oo LOR EXPLANATION OF THE PLATES. Puats XL. . Aphneus estivus, n. sp., p. 428. . Ypthima complexiva, 2, n. sp., p. 423. . Charaxes agrarius, 3, 0. sp., p. 425. . Nilasera apella, $, n. sp., p. 429. . Bireta galbana, nu. sp., p. 438. Leucania byssina, n. sp., p. 442. Mestleta baccalix, nu. sp., p. 452. Dabarita icterica, n. sp., p. 439. . Susica cosmiana, 2, n. sp., p. 440. . Radinacra variana, n. sp., p. 444. Prats XLI, . Eupterote ignavus, 3, 0. 8p., p- 440. . Hypotia allalis, n. sp., p. 462. . Chilo ortellus, G, u. sp., p. 461. . Jartheza cassimella, G, 0. sp., p. 461. Pradatta beatrix, n. sp., p. 442. . Jartheza cassimella, 9, p. 461. . Sterrha paulula, n. sp., p. 456. . Setomorpha tineoides, n. sp., p. 465. . Tinea subochraceella, nu. sp., p. 464. . Alavona minor, 3, nu. sp., p. 464. » @; p. 464. . Leucinodes auxialis, n. sp., p. 458. . Glyphodes fessalis, n. sp., p. 459. . Tarache nivosa, n. sp., p. 446. Proc. Zoou. Soc.—1886, No. XXXI. 31 (Plate XLI. Hind wings greyish, 466 DR. R. W. SHUFELDT ON Nov. 16, 2. Contributions to the Anatomy of Geococcyx californianus. By R. W. Suurept, C.M.Z.8. [Received June 28, 1886.] (Plates XLII.-XLV.) The investigations I am enabled to record in the present paper have been made possible through the kindness of Mr. W. F. Peacock, of Marysville, California. This gentleman on the 23rd of July, 1885, came into possession of a fine male Geococcyx, which had been captured for him alive by a man who had run the specimen down on horseback. Mr. Peacock, having been informed by me that I only desired the skeleton of the species, killed and eviscerated it, and filled the abdominal cavity with powdered charcoal and pyroligneous acid, which preparation brought it safely into my hands after three days’ travel during the most sultry weather. Upon receiving it I at once consigned it to a vessel containing strong alcohol; so that, at this date (May 1886), the specimen is before me in excellent condition. Owing to the fact, however, that it has been eviscerated, I am unable upon the present occasion to say anything about those organs which are situated in the thorax and abdomen, and will confine myself principally to examinations of the muscles of the limbs, the carotids, the trachea (if it be not injured), and the pterylosis. It will be remembered by those who are familiar with my work that I have already published a full account of the skeleton of Geococcyx elsewhere *, and to that paper the present memvir may be considered a second instalment. ; Just now I am far removed by many thousand miles from the libraries and museums, and in a country where such American forms as might with profit be compared with our present subject do not occur. I have by me, however, an excellent field library, consisting of many of the standard anatomical works, including the collected “*Scientific Papers’? of Garrod and Forbes. Neither of the last- named anatomists have anything to say about our Ground-Cuckoo, and I am inclined to think that neither of those untiring workers in avian morphology ever came into possession of such material. Further, so far as my memory serves me, no one has yet paid any special attention to the structure of Geococcys« californianus. This being the case, I have reason to hope that my present contributions will not come amiss. Garrod’s investigations upon the anatomy of the Cuculide demonstrated the fact that both of the carotid arteries are present in .these birds (Coll. Scientif. Papers, p. 169). His statement to this effect is based upon his having examined the following species :— 1 Journ. of Anat. and Physiology, Lond. vol. xx. pt. 2, Jan. 1886, pp. 244— 266, pls. vii., viii., and ix. atid anette IS8b. | GEOCOCCYX CALIFORNIANUS. 467 Cuculus canorus, Cacomantis sepulcralis, Chrysococcy2 sp., Centropus senegalensis, Guira piririgua, Pheenicophaes sp. The same authority finds the accessory femoro-caudal muscle present in :— Oentropus senegalensis, Centropus phasianus, Guira piririgua, Pheenicophaes sp., and absent in the following species :— Cuculus canorus, Chrysococcy& sp., Cacomantis sepulcralis. Of this latter peculiarity Mr. Garrod said, “ Amongst the Cuculide, the Ground-Cuckoos (Centropus, Guira, Phenicophaes) differ from Cuculus and its allies in having the accessory femoro-caudal developed, whilst it is absent in the latter, their respective formulz being AB. XY., and A. XY. This peculiarity, when added to those in the pterylosis, justifies the division of the family into two subfamilies, which may be termed the Centropodinz and the Cuculinz ” (oe. cit. - 210). i According to this author, the ambiens muscle also being present in the Cuculidee it throws this group into the subclass named by him the Homalogonate ; and Mr. Garrod brings forward his very interest- ing researches upon the plantar tendons in birds to still further support his classification of this particular group. The arrangement of these tendons I will again reter to further on. Cuculidee have the czeca also present and possess a nude oil-gland. To briefly recapitulate, then, the above and a few other structural characters of this group brought to light by this talented investigator, we find that the Cuculide are homalogonatous birds with two carotids ; with the sciatic artery the main one in the leg (except Centropus) ; Ciconine, as regards the presence of the expansor secundariorum muscle (see Garrod’s Coll. Scientif. Papers, pp. 323- 29); and finally, as I say, have a uude oil-gland and the ceca. Forbes examined specimens of Geococcyx affinis, and showed some interesting points in regard to the bursa Fabricii, which in the Cucu- lide he says “presents a very characteristic shape, the peduncle being long and thin, and the extremity club-shaped, giving the whole somewhat the appearance of a shortened and clumsy antenna of a butterfly. It disappears completely in adult birds” (Forbes’s Coll. Scientif. Papers, p. 11). This author, on the page of the work quoted, presents us with a figure of the cloaca and bursa of Geococcyx affinis. 31* 468 DR. R. W. SHUFELDT ON [Nov. 16, At the present time, the American Ornithologists’ Union place the Cuckoos of this country in an order Coceyges, having three sub- orders, the Cuculi, the Trogones, and the Aleyones, our genus Geococcyx falling into the first under the subfamily Coccygine, there being one other associated with it, the genus Coccyzus. : Not long ago I showed some of the peculiarities of the coloration and extent of the naked skin-tracts upon the head of this bird’; I regret to say, however, that I have not at hand an account of the pterylosis of the Cuculidz, so on the present occasion I must content myself with an accurate description of that feature in Geococcyx californianus, and leave the comparisons to be made by others who may be more fortunate in this respect. Of the Pterylosis of Geecoccyx. So carefully have I drawn the two views of our subject, which are presented in Plate XLII., showing the pterylee and their exact limits and extent, that a few words will suffice to complete the description. It will be seen that the “capital area” is quite complete, being broken only by the naked and coloured skin-tracts about the eye and on the back of the head. These latter vermilion-tinted skin areas are divided in the median line behind by a very narrow pteryla, which is directly continuous with the posterior middle strip of an equal width, and which terminates at the root of the neck, where it is somewhat abruptly lost in a central, sparsely scattered tract, just anterior to the spinal pterylosis. This posterior cervical strip is continuous above with the capital area. Upon the anterior cervical region we find the tract quite broad above, where it is continuous with the feather-tracts of the gular space; but as we proceed down the front of the neck this tract bifurcates at about halfway between the trunk and the throat, each separate strip thus formed being extended on either side to a point opposite a clavicular head, where it merges into the “ ventral” and ‘‘ humeral tracts.” A “ humeral tract ” is but faintly marked in our Ground-Cuckoo ; and it is seen to pass, on the posterior aspect of the brachium, from the shoulder toward the elbow, but is gradually lost before it arrives at the latter point (Plate XLII. fig. 1). The “ventral tracts ’’ are very broad anteriorly, and are bounded mesially by curved lines, which overlie the clavicular limbs. These tracts, on either side, also bifureate as we proceed in the direction of the abdomen. The outer strip grows gradually narrower, and makes a graceful curve round under the arm-pit, below which it abruptly terminates. The mesial strip formed by the bifurcation of the ventral tract is long and narrow, being gently convex outwards for its entire length. The distal extremities of these strips become extremely slender as they converge towards the vent, around which they pass to merge with each other behind this. opening, and with the feather-tract covering the underside of the coccygeal protu- berance (Plate XLII. fig. 2). 1 This, 1885, pp. 286-288, pl. vii. 1886. | GEOCOCCYX CALIFORNIANUS. 469 The spinal pterylosis is represented by two broad, longitudinal tracts well separated from each other in the middle line by a naked- skin area overlying the vertebral column. These spinal pteryle gradually converge towards each other as they approach the pelvic region, over which they merge into one feather-space, which becomes pointed behind and terminates just in front of the nude oil- gland. The upperside of the coccygeal protuberance is also sparsely feathered, being divided from a more generously covered area below by the line of horizontally arranged pits for the quill-butts of the rectrices of the tail. An exceedingly narrow tract, on either side, springs from the posterior margin of the outer bifurcation of the ventral tract just below the arm-pit, to run longitudinally down the side, in front of the thigh, to become lost before it arrives at the margin of the vent. This strip seems to be composed simply of a double row of feathers, and might appropriately be termed the lateral tract. The patagium of the arm is very thinly feathered anteriorly, while its dorsal aspect is quite completely covered ; the remainder of the pterylosis of the pectoral limb presents us with nothing of a peculiar nature. The posterior marginal- boundary of this “ alar tract”’ is, as usual, terminated by the row of quill-butts of the primary feathers of the wing. Passing now to the crural region, we find a posterior limb but sparsely feathered, while a conspicuous ‘‘ femoral tract’ extends obliquely across the dorsal aspect of the thigh, and rapidly narrow- ing, runs along the pubic line, finally merging into the “ caudal tract.’ Geococcyx shows its best-marked apteria in front, in the mesial space between the inner strips of the ventral tracts, and laterally to the outer side of the spinal pterylosis, where, indeed, for a con- siderable space no feathers may be said to occur at all. A well- marked dorso-longitudinal naked area is also to be seen. In this Ground-Cuckoo we notice a membrane, stretching between the thigh and leg, which corresponds to the patagial fold of the pectoral limb, and fully as well-developed. Before closing this part of our subject it is of interest to observe the general form of Geococcyx, which, now that its feathers have been removed, can be studied to the best advantage. It will be seen how perfectly its figure has come to assume a shape best adapted to the peculiar requirements of the bird. Its pelvic limbs are large, muscular, and consequently powerful, while the pectoral ones are decidedly less so, though by no means weak or inefficient. The body-form of this prince of avian racers is what almost might be called “clipper built,” so admirably fashioned is it to the needs and ends of a rapid running bird of the size of our subject. With these few remarks upon the external organization and appearance of Geococcye we will now close this part of our discussion, and pass to the consideration of some of the features presented in the structure of the remainder of its economy. 470 DR. R. W. SHUFELDT ON [Nov. 16, On the Mode of Insertion of the Patagial Muscles of the Pectoral Limb. Having considerable faith in the value in classification of the arrangement of the insertional extremities of the tendon of the ¢ensor patagii brevis muscle, and the forms of the patagial muscles gene- rally, as single characters, it was with no little interest that I carefully removed with my scalpel the integuments over this region, for the first time in my experience in Geococcyx. The late Mr. Garrod’s excellent work in this direction is now familiar to all ornithologists ; but on this occasion I refrained from consulting any of the accurate drawings he has left us illustrating these parts in many groups of birds until I had actually completed my dissection, and my drawing of it, which is shown in Plate XLIII. fig. 2. I then opened his “‘ Collected Scientific Papers” and proceeded to compare my figure with his numerous illustrations of the same dissection among other birds. Being familiar with the arrangement of this tendon in a great many North-American birds from my own labours, I was confident that the condition of things in Geococcy« californianus was a marked departure from anything I had previously met; nor did I expect to find anything in Garrod’s illustrations that would prove to be exactly like it. But in this last hope I was very agreeably disappointed, for I find that it corresponds almost exactly with the state of affairs found by this talented anatomist to be present in certain Galbulidee. To satisfy one’s self of this fact it is but necessary to compare my figure with the Jacamar dissected by Mr. Garrod, as shown in his work (plate 23. fig. 1, tendon of tensor patagit brevis in Urogalba paradisea), and the striking resemblance will be at once appreciated. He has simply cleared his tendon more completely of its investing fascia than I have, and still further separated its several slips; while in my figure of Geococcyx the tendon is shown as it presents itself immediately after turning back the integuments, or, in other words, exactly in situ. The liberty taken by Mr. Garrod to still further show these slips and their exact insertions is perfectly permissible, and often resorted to for the purpose named. It will be seen that after the tendon of the tensor patagii brevis arrives over the proximal third of the belly of the extensor metacarpi radialis longior muscle in Geococcyx it trifurcates, one slip passing downwards to become inserted immediately below and on the outer aspect of the ewtensor carpi ulnaris muscle; the shortest slip at once attaches itself to the ewtensor metacarpi radialis longior, while the longest division of all passes with the last-named muscle to become inserted with it upon the outer condyle of the humerus. As for the muscular portion of these patagial muscles above in this Ground-Cuckoo, I have represented them with the arm turned somewhat differently than the position Mr. Garrod was wont to give it. It will be seen, however, that the bulk of this muscular portion in oe as in Urogalba, belongs to the tensor patagii brevis muscle, 1886. | GEOCOCCYX CALIFORNIANUS. 471 It is still further interesting to compare the arrangement of these tendons in Geococcyx with the similar structures as they were found to exist by Mr. Garrod in Upupa epops and Cuculus canorus, both of which are figured upon the same plate alluded to above. We at once observe that our subject differs considerably in these particulars not only from the Hoopoe, but still more from the Cuckoo. Indeed, so far as Upupa is concerned, it simply lacks the long slip going to the humeral condyle in order to make the arrangement of the insertional extremities of the tensor patagii brevis agree with the corresponding arrangement as found in my specimen of Geococcyw. So far as this one character is concerned, then, it points to the fact that a certain affinity exists connecting our Geococcyx with the Galbulide. ji Fig. 1. Fig. 2. Fig. 1. Muscles at the outer side of the elbow of the right wing of Caprimulgus europeus. Fig. 2. The same of the left wing of Steatornis. (Both figures after Garrod.) tpb, tensor patagii brevis; ecr, extensor carpi radialis (extensor meta- carpi radialis longior of the present writer); 0, biceps; d, deltoid ; ¢, triceps ; 2, humerus. Further, the marked difference in this particular between Geo- coccyx and Cuculus canorus is not to be overlooked. Now, strange to say, there is still another (and what we must believe to be a widely separated) group of birds that possesses an arrangement of the insertional extremity of the tensor patagii brevis very much as we find it in our present subject. ‘These are no others than the Caprimulgi. I reproduce (figs. 1 & 2) Prof. Garrod’s figures of these parts in Steatornis and Caprimulgus europeus, the better to show this simi- larity. It will be seen in these Caprimulgine birds, however, that the lowest slip merges with the fascia to the outer side of the ulna, while in my specimen of Geococeyw it goes to the extensor carpi ulnaris muscle. Garrod pointed out another character of some value, which he 472 DR. R. W. SHUFELDT ON [Nov. 16, discovered during his dissections of the arms of birds ; this was the presence or absence of the expansor secundariorum muscle (Coll. Sci. Papers, p. 323). As this delicate muscle and its tendon is well developed in the Storks, he, for convenience sake, termed it the Ciconine character. He found the Cuculidze to be Ciconine birds so far as this structure was concerned, but I find after a very careful search in both pectoral limbs of my specimen of Geococcyx that this character is missing in it. This, then, constitutes another difference between Geococcyx and the Cuculide. Of the Pectoral Muscles. All three of the pectoral muscles are present in this bird, and all conspicuously developed, although the pectoralis tertius is consider- ably larger in comparison than is usually the case. Their muscular fibres are remarkable for their fine texture and compactness, both of which qualities, added to their pale colour, lend to these structures a very delicate appearance. Nothing of a peculiar nature seems to distinguish either the pectoralis major or secundus, as they both arise and are inserted ina manner common to the majority of the class. On the other hand, the pectoralis tertius, although inserted as we usually find it in birds, has no sternal origin, but arises from the externo-anterior aspect of the sternal extremity of the coracoid, as well as from the side of the shaft of the same bone. Recent dissections of mine, performed upon various species of the Corvidee, go to show that in them this muscle has quite an extensive origin upon the sternum, and its bulk sinks into insignificance when compared with the size of the great pectoral as it exists in all of the species of this latter group which I have examined. On the Myology of the Pelvic Limb in Geococcyx. Quite recently I have completed a very extensive chapter on the muscles of birds, and the MS. of this piece of work, with the nearly one hundred woodcuts that illustrate it, are at hand at the present writing. So with the bird now before us I will, without further explanation, adopt the myological nomenclature which I have proposed in my MS., without discussion of such points as wherein I may differ in homologies or terms with other authorities. Such differences, and I trust they may be few and well sustained, must be left for decision until such time as the work referred to appears in type. It is my aim here to enter quite extensively into the description of the muscles of the pelvic limb of Geococeyx, as they offer us many points of interest. We find the sartorius muscle (Plate XLIV. fig. 1, 8) powerfully developed in Geococcyx, as are the majority of the muscles of the thigh in this bird. It arises, semitendinous, from the crest of the neural spine of the last vertebra of the dorsal region of the spine, from the summit of the anterior portion of the crista of the sacrum, and from the adjacent surface of the superior aspect of the ilium on the cor- 1886. ] GEOCOCCYX CALIFORNIANUS. 473 responding side. The fibres, forming an oblong and rather thick muscle, pass downwards and backwards to the region in front of the knee. Here it becomes inserted by a special slip of fascia that is thrown off and merges with the general fascia surrounding the knee- joint ; and, secondly, by a more carneous insertion into the inner half of the superior rim of the cnemial crest of the tibia and the continuous inner margin of the summit of that bone. The sartorius bounds anteriorly the superficial group of muscles of the thigh; consequently its anterior border is free. Its posterior border above unites quite intimately with the overlapping gluteus primus muscle ; while this border below is sharp and free, although here, too, the gluteus also overlaps it, and a delicate connective tissue binds them together. The gluteus primus (Plate XLIV. fig. 1, g/.pr) constitutes that great and rather complex muscle which makes up the central fleshy portion of the outer aspect of the thigh. It arises by a strong fascia from the summit of the coossified neural spines of the anterior sacral vertebrae, and by carneous fibres from the outer rim and under surface of the whorl-like, overarching portion of the ilium behind ; and finally from the contiguous portion of the pelvis over the anti- trochanter, between these anterior and posterior origins. In front the muscle consists first of a strong layer of semitendinous fascia, which closely overlies the gluteus medius muscle beneath it, and overlaps the sartorius anteriorly. The posterior origin and mid- division become rapidly carneous and more massive as we proceed in the direction of the caudal extremity of the body. So that, where we find it arising from beneath the overarching part of the ilium behind, the muscle fills about one fourth of the convexity there formed, the semitendinosus filling the remainder of this curious cavity. The fibres of the strong, semitendinous, muscular sheet springing from these several origins, or rather along this continuous line of origin, now pass, converging as they do so, towards the anterior aspect of the knee-joint. The semitendinous portion anteriorly be- comes fleshy as it arrives along the outer pelvic margin, with which it is quite intimately connected. The hinder division of the muscle remains thick and carneous until it comes to the Knee-joint. Here all the fibres again become tendinous and fascia-like, and, uniting with a similar structure contributed by the evtensor femoris lying beneath it, the combined sheath thus formed surrounding the well- developed patella, closely invests the front and sides of the knee- joint, and is finally inserted all round the anterior and externo- lateral borders of the summit of the tibia. The most superficial muscles of the leg are the gastrocnemius and the peroneus longus. As we would naturally expect, the gastrocnemius muscle (Plate XLIV. fig. 1, y) in Geococcyx is wonderfully well-developed. All three of its heads are strongly defined, and the fleshy belly of the muscle is massive and thick. Its ewternal head arises, curiously enough, by two perfectly distinct tendinous slips. One of these, a strong, flat tendon, comes off from 474 DR. R. W. SHUFELDT ON [Nov. 16, the outer surface of the external condyle of the femur, while the second slip, also strong but somewhat more rounded, arises from the back of the external femoral condyle, just above the trochlear surface. Between these two tendons of the external head of the gastrocnemius we find the loop for the diceps and the tendon of that musele itself, the loop being quite intimately attached to the free edge of the outer tendon. Below the loop, these tendons merge with each other and terminate in the commencing fibres that compose the external head of the gastrocnemius proper. The internal head of the gastrocnemius, or what is really the middle head in birds, is quite median in position, and is represented merely by a long, narrow, muscular slip that arises by a delicate, though strong, cord-like, tendon from the middle of the intercondyloid notch of the femur. The tibial head of the muscle under consideration is massive in its dimensions when compared with the divisions of origin of the gastrocnemius already described. It arises fleshy from an extensive surface on the inner aspect of the head of the tibia as high up as the marginal boundary of its summit; and from the muscular fascia surrounding certain of the deep thigh-muscles, which are inserted into the distal end of the femur, and consequently are adjacent to the posterior aspect of the head of the tibia. At a point about opposite the junction of the upper and middle third of the shaft of the tibia the internal and tibial heads of the gastrocnemius merge with each other, while between their free edges above passes the exceedingly delicate tendon of the semimembranosus muscle. All of the fibres of this complicated origin of the gastrocnemius muscle now converge and pass directly down the back of the leg of the bird. They also merge with each other in such a manner that, were we to examine the muscle at about the middle third of the leg, we would find it composed of two well-defined bellies, rather thin, nearly of equal size, united somewhat firmly by an intervening fascia, and each being convex on their superficial aspect and the reverse on their under sides, which concavity accurately moulds itself to the deeper layer of muscles of the leg, which the gastrocnemius com- pletely covers. At the lower fourth of the tibial shaft the fibres terminate in a broad, flat, and glistening tendon, which passes flat-wise over the shallow and longitudinal groove of the ¢ibial cartilage, at which point the tendon is considerably thickened. Next, crossing the tibio-tarsal joint, it becomes internally attached to the hinder surface of the hypotarsus of the metatarsal bone, below which protuberance it finally merges into the deeper layer of the podothecal sheath con- fining the flexor tendons. The peroneus longus (Plate XLIV. fig. 1, p.l) arises from the entire free margin of the cnemial crest in front of the head of the tibia, and by somewhat specialized, though delicate, tendons, one each from the apices of the pro- and ectocnemial processes of the same part of the bone. These latter tendons pass down on the under surface —- 1886. ] GEOCOCCYX CALIFORNIANUS. 475 of the muscle, which latter must be cut across and reflected in order to discover them. From this origin the peroneus longus as a rather thick, coneavo-convex muscle passes down in front of the leg, its outer edge dipping down for attachment between the tibialis anticus muscle, which it almost completely covers, and the flexors to its outer side ; its inner edge is free and thin, and overlaps the gastrocnemius. Low down on the outer side of the tibial shaft the fibres of the peroneus longus have converged to terminate in a small narrow tendon, This tendon, just above the condyles of the tibia, bifurcates, the short slip of the bifurcation going to the fascia covering the block of cartilage (which I have termed the tibial cartilage) at the back of the tibio-tarsal joint for attachment, while the longer slip passes across the articulation to the bundle of tendons at the back of the tarso-metatarsus to merge with one of the special flexors. Removing this superficial layer of muscles of the pelvic limb and turning our attention once more to the thigh, the following ones are presented to our view for examination :— The gluteus medius muscle (Plate XLIV. fig. 2, gl.m) is found to be strong and tendinous. It, as in all of the birds that I have examined, fills the concavity of the preacetabular portion of the pelvis, and here in Geococcy# extends laterally much beyond the bone, as this bird has a very narrow pelvis anteriorly, while it demands the use of a powerful set of gluteal muscles. The gluteus medius arises by a strong, flat tendon from the superior surface of the outer moiety of the anterior iliac margin, by a dense fascia from the entire line bounding the preacetabular concavity, and finally by fleshy fibres from the upperside of the ilium itself. The fibres of the roundish muscle thus formed converge as they pass to the caput femoris, and, just before arriving at the bone, they terminate in a dense flat tendon, which, passing over a bursa, is inserted at a point on the antero-external aspect of the femoral trochanter. The gluteus minimus (Plate XLIV. fig. 2, g/.min) is a very much smaller muscle than the gluteus medius, and is found immediately beneath it to its outer side. In form it is oblong, and fully three times as long as wide. It arises from the outer superior surface of the fore part of the ilium, and passing obliquely downwards and backwards as a flat narrow band of fibres, it becomes inserted by semitendinous ones on the outer aspect of the upper third of the femur, just below the trochanter. This muscle may also ride over a small bursa, just before it arrives at its insertion. The extensor femoris is readily divisible at its lower half into two parts, the bulkier anterior one representing the erureus (Plate XLIV. fig. 2, c), and the posterior division the vastus externus (Plate XLIV. fig. 2, V.£). As awhole, this powerful extensor of the leg upon the thigh arises from the antero-external aspect of nearly the entire length of the shaft of the femur, and from a portion of the trochanter at its summit. At about its lower fourth it terminates in a broad tendinous expansion, which, as has already been described, is amply reinforced by other insertional portions of the superficial muscles of the thigh. 476 DR. R, W. SHUFELDT ON [Nov. 16, The patella is found encased in front in this great tendinous sheath of the knee-joint, and below the apex of this sesamoid we find the enveloped track of the tendon of the ambiens muscles, as it passes round in front of the femoro-tibial articulation. The combined tendon of the extensor femoris is finally inserted into the cnemial crest of the tibial and the lateral boundaries of the summit of that bone. Some of the superficial muscles on the outer side of the leg are so extended as to take a certain amount of their origin from this great tendinous expansion. In Plate XLIV. fig. 2 I have very thoroughly divided these two sub- divisions of the extensor femoris, in order to show their relative size, as well as their relation to each other and the surrounding structures. The biceps flexor cruris (Plate XLIV. fig. 1; fig. 2, Bz) arises by carneous fibres upon quite an extensive portion of the under surface of the over-curled part of the ilium behind the acetabulum, and by along tendinous slip which comes off from the free anterior margin of this part of the ilium. ‘The fibres converge as they pass downwards, and unite to form a somewhat flattened muscle. Opposite the head of the tibia, the biceps terminates in a round tendon, of cord-like dimen- sions, which passes through a special loop to make its way between some of the muscles at the back of the leg, to become inserted on the tubercle intended for it on the outer side of the superior moiety of the shaft of the fibula. The loop of the diceps (Plate XLV. fig. 1,7) is flat and fashioned like a delicate tendinous ribbon. Its upper end arises from the side of the shaft of the femur above the external condyle, while the lower end comes off from this protuberance just below the insertion of the outer slip of the external head of the gastrocnemius muscle. A branch of the sciatic nerve also passes through this loop in company with the tendon of the biceps. The semitendinosus (Plate XLIV. figs. 1, 2, St; Plate XLV. fig. 1, St) isa marvellously well-developed muscle in this form, as is also its accessory head. Its origin fills about three fourths of the nether cavity formed by the posterior overarching portion of the ilium, under which it arises. Posteriorly, the fibres forming its free margin are so arranged as to create a rounded border; the lower end of its are terminating about opposite the post-pubis of the pelvis. From this origin the fibres of the semitendinosus pass downwards and forwards as a great, though somewhat compressed muscle. When within rather more than a centimetre’s length of the shaft of the femur, they terminate in an oblique tendinous raphe, which latter forms the bounding-line between this muscle and the next. The accessory semitendinosus (Plate XLV. fig. 1, a.s.¢) is com- posed of coarser fibres than the muscle just described. It springs from a longitudinal line occupying the distal half of the shaft of the femur, and from the upper surface of the hinder aspect of the external condyle of that bone. The fibres pass backwards and a little upwards to become inserted into the tendinous raphe just alluded to. The lower extremity of this tendinous raphe terminates, in Geococeyx, in a thin, flat, and delicate tendon, which continues down- 1886. ] GEOCOCCYX CALIFORNIANUS. 477 wards and forwards to the inner surface of the head of the tibia, where it becomes inserted, the point of insertion being found above that of the semimembranosus muscle, the insertional tendon of which overlaps it. The semimembranosus (Plate XLIV. figs. 1,2; Plate XLV. fig. 1, Sm) in Geococcyz, though thoroughly developed, is rather a slender and thin muscle, markedly so when we compare it with the massive semitendinosus which overlies it. It arises from the outer surface of the ischium, for its posterior two thirds, on a line situated a few millimetres above the lower free edge of that element of the pelvis. The fibres gradually converge as they pass downwards and forwards, to terminate in a very delicate and thin ribbon-like tendon, which, passing between the broad tibial head of the gastrocnemius and the proximal extremity of the shaft of the tibia, becomes finally thereupon inserted on its internal surface. The hinder margin of the semimembranosus is free, while its border anteriorly is juxtaposed to the posterior edge of the adductors. In the bird before us the ambiens muscle (Plate XLV. fig. 1, amb) is conspicuously developed. It arises from the apex of the prominent prepubic spine of the pelvis, and the fibres passing directly down to the inner side of the femur, and parallel with that bone, form a strong fusiform muscle. As it approaches the patella it terminates in a small flattened tendon, which, piercing the fascial envelop of the knee-joint below the inferior apex of that sesamoid, passes round the joint, to become finally lost to the outer side and opposite the summit of the tibia, where some of its tendinous fibres merge with the fibres of origin of the flexor perforatus digitorum, or, at least, with one of its divisions. The améiens is overlaid by the sartorius muscle, and in the figure is brought into view only through the aid of a small dissecting-hook and chain, which pull it forwards in order that it may be better seen. The femoro-caudal muscle and the accessory femoro-caudal are both present and fully developed. The femoro-caudal (Plate XLY. fig. 1, f.c) arises, tendinous, from the lower posterior border of the pygostyle. It soon becomes fleshy and as a narrow, muscular ribbon passes through the tissues over- lying the lateral group of caudal muscles proper. Opposite the posterior border of the pelvis it expands to form a prettily-shaped and compressed spindle, closely covering the obturator externus muscle and the side of that bone. As it nears the femur it again contracts, receives the fibres of its accessory head, and is finally inserted upon the femoral shaft, at the posterior aspect of its prox- imal third. The accessory femoro-caudal (Plate XLV. fig. 1, afc) arises be- neath the overarching part of the postacetabular portion of the ilium, just behind the acetabulum and beyond. Its fibres pass obliquely downwards and forwards to join with those of the JSemoro-caudal, and to become inserted with them into the upper part of the femur as already described. The obturator ewternus (Plate XLV. fig. 1, 0.e) arises from the outer surface of the ischium above the “obturator space,” the 478 DR. R. W. SHUFELDT ON [Nov. 16, muscle being thin and closely pressed to the pelvis. The fibres converge as they near the femur and terminate in a strong, flat tendon which becomes inserted on the outer aspect of the trochanter of that bone, which insertion is slightly overlapped by the tendon of the gluteus medius muscle. The adductors arise from the infero-external margin of the ischium, between the anterior edge of the semimembranosus and the obturator foramen. The adductor longus (Plate XLV. fig. 1, a./) is the more anterior of the two and consequently arises the higher on the pelvis, and comes off in front of the adductor magnus, which it largely overlaps. Its fibres pass obliquely to the posterior aspect of the shaft of the femur, down which they become inserted as far as its middle, along the linea aspera, a line which is well marked in our subject. The adductor magnus (Plate XLV. fig. 1, a.m), like the one just described, is also a broad ribbon-like muscle, arising from the ischium between the semimembranosus and a middle point on the underside of the adductor longus, close up to its semitendinous origin. Anteriorly its margin is free, while posteriorly it is juxtaposed to the anterior border of the semimembranosus. Passing parallel with those of the other adductor, its fibres are inserted into the distal moiety of the linea aspera of the femoral shaft, down to the intercondyloid notch of that bone, where this muscle makes a very substantial insertion. Removing all the muscles of the thigh thus far described, we find that in this region we have the following ones remaining. They are shown in my drawing (Plate XLV. fig. 2), together with a few as yet undescribed muscles of the leg. A very important muscle is the obturator internus (Plate XLY. fig. 2, 0.2), and in Geococcyx it exists as we find it in the majority of the class. Prof. Garrod laid some stress on the point whether this muscle arose from a triangular or an oval area. Here it arises from a decidedly oval one, and as usual this is from the mesial sur- faces of the ischium and the post-pubic element of the pelvis. Its tendon emerges from the obturator foramen, and overlapping the gemellus muscle, passes to the outer aspect of the upper part of the trochanter of the femur, where it is inserted. The gemellus (Plate XLV. fig. 2, ge) is a short, thick, carneous muscle, which arises about the outer rim of the obturator foramen of the pelvis. Its fibres passing obliquely upwards and forwards are in- serted with the tendon of the obturator internus muscle on the tro- chanter of the femur. This bird also has a few of the fibres of its gemellus muscle inserted into the tendon of the obturator externus muscle, at least I found this to be the case in the specimen before me. We find the vastus internus (Plate XLV. fig. 2, v.i) to be a strong, fusiform muscle, that is only fully discovered after we have removed the ambiens and the adductors. It lies on the postero-internal aspect of the shaft of the femur, arising from the linea aspera nearly as high up as the head of that bone, and increasing in bulk as it descends, still making attachment to the linea aspera, it only becomes free just above the condyles. At this point it terminates in a flat tendon, which, crossing the articulation of the knee, becomes inserted into the — 1886.] GEOCOCCYX CALIFORNIANUS. 479 front part of the inner marginal rim of the summit of the tibia. This muscle constitutes a powerful auxillary to the action of the extensor femoris, and it appears to be quite a constant one in the class Aves. The description of the vastus internus completes our account of the musculature of the thigh. A brief recapitulation of them shows us that Geococcyx possesses in this region all of the muscles that we usually find there in birds. The entire group including the amdiens, the femoro-caudal, the accessory femoro-caudal, the semitendinosus, the accessory semi- tendinosus, and the semimembranosus, so ably introduced into taxonomy by Garrod, are all present and wonderfully well developed. Then we have all three g/wtei represented, with an ample evfensor femoris, and its auxiliary the vastus internus, a handsome biceps flewor cruris, with its interesting pulley at the back of the knee. Next, the two obturators and the gemellus; and finally two powerful adductors, the magnus and longus. We may now once more direct our attention to the leg, and investigate the muscles there found in its second layer. First among these stands the tibialis anticus (Plate XLIV. figs. 1, 2, tib.ant). This interesting muscle arises, as most commonly among birds, by two very distinct heads. The under and at the same time the smaller one of these comes off by a tendon from a little pit that is found on the anterior aspect of the external condyle of the femur ; the second or larger portion of the muscle completely covers over the first, except of course its tendon, which extends further up. This latter head arises from a line extending all round within the cnemial crest and the pro- and ectocnemial ridges of the tibia. The fibres of the two heads extend directly down in front of the tibial shaft, at the lower third of which they gradually merge with each other, and finally terminate in a strong tendon, which, passing through the oblique fibrous loop, or bridge rather, at the front and lower end of the tibia, pass across the tibio-tarsal joint, to become inserted on the anterior surface of the upper third of the tarso-metatarsus bone, just below its head. The soleus (Plate XLV. fig. 2, so), found at the back of the leg, is another well-developed muscle of this layer in Geococcyz californi- anus. It arises from behind the tibia, on its inner side, and just below the marginal rim of its summit. The fibres at once form a little flat muscle, rather longer in shape than the fish from which it derives its name, and soon terminate at the lower or tail-end in a tendon. This tendon, long and narrow, passes directly down the postero-internal aspect of the leg to become inserted into the dense fascia covering the tibial cartilage at its supero-internal angle. Great care and patience are necessary in the study of the arrange- ment and distribution of the tendons of the flexors and extensors in the leg and foot of a bird, and to this rule Geococcyx by no means forms any exception. In describing these I will present them in the order that they most conveniently came under my hand after the removal of the muscles alluded to in the foregoing paragraphs. 480 DR. R. W. SHUFELDT ON [Nov. 16, After we have cut away the ¢ibialis anticus, we find another, and only one other, muscle occupying the anterior aspect of the tibia. This is the extensor longus digitorum. The extensor longus digitorum (Plate XLY. fig. 1, e./.d) arises from the anterior aspect of the in-half of the tibial shaft as high up as the ¢idialis anticus muscle, which covers it; it also arises from a tense fascia which comes off from the lower free edge of the pro- cnemial crest of the tibia; and finally from a longitudinal line ex- tending obliquely down the front of the shaft of the tibia to its lower third. This obliquity finally brings the tendon in which the extensor longus digitorum terminates to the middle line. Just above the condyles of the tibia, it here passes through the little bony bridge ; emerging from which it crosses the ankle-joint in front, then passes down the anterior aspect of the tarso-metatarsus bone, overlying the short extensor. At the upper end of this last- named bone, and over the ankle-joint, this tendon is firmly bound down by a fibrous fascia. In some birds we know a special bony span exists for it on the upper part of the tarso-metatarsus, as in certain Owls. When the tendon of this muscle arrives at the anterior aspect of the trochlew of the distal end of the tarso-meta- tarsus, it expands and bifurcates. The tendinous expansion becomes more or less attached to the underlying tissues, while each bifur- cation passes one over the second, and the other over the third toe, for their entire lengths, to become inserted into the upper points of their ungual phalanges. Now from the side of the tendon that goes to the third toe another slip is differentiated off in a very peculiar manner, owing to the reversion of the toe in question. For it not only passes over the top length for insertion of this fourth digit, as in the case of the others, but its slip also splits off to make a separate insertion at the extremity of the basal phalanx of the third digit. I have had the opportunity of dissecting three feet, with the view of studying this point, and I find it to obtain in all of them. The extensor brevis digitorum (Plate XLV. fig. 1, e.6.d). Thisisa muscle I find that, in common with many other authors, I have de- scribed in my MSS. as the extensor hallucis brevis, from the fact that its tendon goes to the hallux alone. But here, so extraordinary is its development, that no such term would be either adequate or appro- priate. Even here the short extensor of the hallux has a certain amount of individualization, though it is not fully differentiated from the other part of this extensor brevis. It, however, is not attached more than halfway down the anterior aspect of the shaft of the tarso-metatarsus, at which point it terminates in a delicate thread- like tendon; this passes directly over the upper border of the accessory metatarsal, and along the top of the basal joint of the hallux, to become inserted in the usual manner in the base of the claw-joiat. Now the remainder of the ewtensor brevis digitorum is attached down the shaft of the tarso-metatarsus, as far as the distal trochlez ; the outer portion of it developing a tendon about halfway down, which is concealed by the carneous fibres which overlie it. nie Y 1886.] GEOCOCCYX CALIFORNIANUS. 481 This tendon passes round beneath the trochlea for the fourth toe and is really inserted on the underside of the basal joint of this digit at its proximal extremity ; so that in the case of this toe it seems as though it would act almost as a flewor. With the second and third toes, however, the carneous fibres of the muscle under consideration are continued all the way to the trochleze, where they terminate, in either case, in a strong, flat tendon, which passing over the joint is inserted on the upperside of the proximal extremity of the basal joint. Here, of course, the muscle acts (in the case of the second and third toes) as an auxiliary to the long extensor. Not a little room is here open to us for speculation as to how the tendon of this short extensor in the case of this fourth toe exactly came to assume its present point for insertion, as the digit gradually and finally became permanently reversed. Indeed, the high develop- ment of this short extensor in Geococcyw over the vast majority of the class is, too, an interesting fact; and did the reversion of the digit precede or follow the muscular development? No doubt the completeness of the latter, and its perfection for an avian type, has come about as a demand on the part of the habits of the bird itself and its marvellous fleetness of foot. The tibialis posticus (Plate XLV. fig. 1, ¢ib. post) is a very slender muscle in Geococcyz, but closely resembles the same muscle as I have found it in all other birds which I have examined for their myology. My reasons for terming it the ¢idialis posticus are fully given in my MSS. and will appear in due time. It seems to be one of the peronei of the senior Edwards. As in a number of the Passeres, we find it here to arise from the antero-lateral aspect of the shaft of the fibula below the tubercle for the insertion of the biceps flewor cruris, from the interosseous membrane between the leg-bones, from the contiguous surface of the shaft of the tibia, and, finally, from the fascia separating it from the deep flexors of the leg. The fibres pass directly down the outer side of the tibia as a long, slender, fusiform muscle. At the lower fourth of the shaft of this bone they terminate in a small tendon, which, passing in front of the external malleolus, crosses the ankle- joint to become inserted into the supero-external rim of the summit of the tarso-metatarsus. The flewor perforatus indicis secundus pedis (Plate XLIV. fig. 2, J p,) is even a better developed muscle than I found it to be among typical Corvidee, some of which I have recently dissected, and it is fully as well individualized. It arises from the fascia at the outer side of the knee-joint, and from the contiguous surface of the external condyle of the femur. Here it receives the anastomosing fibres of the extremity of the tendon of the ambiens. The muscle is fusiform in shape and accurately moulded on the flexor it covers at its side. Its tendon in descending the leg is thin and ribbon-like. At the ankle it passes through the tibial cartilage, and crossing the joint goes through, with the second tier of tendons, the cartilaginous cap on the back of the hypotarsus of the tarso-metatarsus. Passing down behind this latter bone, and Proc. Zoot. Soc.—1886, No. XXXII. 32 482 DR. R. W. SHUFELDT ON [Noyv. 16, through the annular ligament in the sole of the foot, it proceeds to the underside of the second toe, beneath the second phalanx of which it expands to form a tubular sheath for the passage of the deep flexor, while at the same time it becomes attached to the side of this joint of the toe in question. The carneous portion of this muscle in the leg is to the outer side of the loop for the biceps flewor cruris, and, owing to the fact that it varies in form and size in different birds, it is as well to bear this in mind. The flexor perforatus medius secundus pedis (Plate XLIV. fig. 2, F.p,), a8 in all of the birds I have examined, is one of the best developed perforated tendons at the back of the leg. Its fascia of origin merges with the enveloping fascia about the knee-joint, while it also arises by a strong tendon, common to it and the flewor perforatus indicis secundus pedis, from the external aspect of the outer condyle of the femur. Finally, it is attached more or less by carneous fibres down the shafts of the leg-bones to a point below their middle, or rather the middle of the leg. Below this the muscle terminates in a strong tendon, which, taking an oblique course through the tibial cartilage, passes as usual over the ankle-joint, through the hypotarsus, and down the back of the tarso-metatarsus. In the foot it perforates the more superficial flexor of the basal phalanx of the outermost of the two anterior toes, then the turn bifureates over the prebasal joint to allow the deep flexor to pass through, these bifurcations becoming the insertions of this muscle, and they are attached to the sides of the shaft of the second joint of the toe alluded to, or the external one of the two in front. The flewor perforatus annularis primus pedis (Plate XLIV. fig. 2, J-p.@) in this bird seems to have acquired a more central position on the back of the leg than in many others that I have dissected, and, moreover, its tendon, as will be seen from the figure, is quite superficial. It arises from between the condyles of the femur by a slight semitendinous slip, and from the side of the flexor longus hallucis. The muscle itself is somewhat of a fusiform outline and rather flat ; it lies to the inner side of the loop for the biceps. About one third the way down the back of the leg it terminates in a small though very long tendon, which, passing quite superficially through the tibial cartilage and over the ankle-joint and hypotarsus, runs in common with the other flexors down the back of the tarso-metatarsus, turns to the rear in the sole of the foot to become inserted on the underside of the distal end of the basal phalanx of the reversed digit. In the specimen before me this insertion is to the outer side of the deep flexor, and the tendon is not slit for its passage. Nothing could be more engaging than the examination of these reversed tendons in the sole of the foot of this Ground-Cuckoo, for the greatest nicety in accommodation has been accomplished as they have gradually come to assume their present position. No doubt some of the departures observed from the more common arrangement of them are due to the reversion of the digit in question. Strong, fibrous bands are so disposed in this plantar region as to 1886. ] GEOCOCCYX CALIFORNIANUS. 483 admirably hold the several groups of flexor tendons in place, and at the same time they act as pulleys for their guidance and afford correct application of the force intended to flex the toes. The flexor longus hallucis (Plate XLIV. figs. 2, fil; Plate XLV. figs. 1, 2, £1.) has two separate heads, the one coming off from the outer side of the external condyle of the femur, and the other, far more fleshy, arising from the posterior aspect of the same bone between the condyles. Above this muscle is overlapped by the more superficial flexors, while in turn it has beneath it the flexor perforans digitorum profundus. About halfway down the leg it gives way to a strong tendon, which, passing deep in the tibial cartilage, crosses the ankle-joint to pass through the outer canal of the osseous portion of the hypotarsus of the tarso-metatarsus. Down the back of the shaft of this latter bone the tendon exhibits a disposition to develop an osseous rod in its continuity, but this does not actually occur in my specimen. It lies in this region just above the tendon of the deep flexor, and, immediately above the sole, makes a fibrous connection with it of some extent, This fibrous “vinculum”’ is in no way oblique as it is described by Garrod for many birds, but passes directly from one tendon to the other for about 8 millimetres, and were it not known that it as a rule passes obliquely from the flewor longus hallucis, it would be quite impossible here to designate which tendon was responsible for the connection. In the foot the long tendon of the Aad/ux passes in the usual way to become inserted on the tubercle at the underside of the proximal end of the ungual phalanx, As its name indicates, our next muscle, the flexor perforatus indicis primus pedis (Plate XLV. fig. 1, f,), has its tendon attached to the nether side of the basal phalanx of the index digit, and consequently aids in bending that toe. Above, as a flat, long muscle, it comes off by a thin tendon from the external surface of the outer femoral condyle, arising with the flewor perforatus medius secundus pedis. We also have in Geococcyx an unusually large flexor perforatus medius primus pedis (Plate XLIV. fig. 2, f,), which here arises by two slips, an outer tendinous one, from the external condyle of the femur, which has a common origin with other muscles there arising and is intimately connected with the dense fascia about the front of the knee-joint ; while the second slip arises from between the femoral condyles, in common with other flexorsthat come off from that point. The two heads are quite independent, but merge with each other before they terminate in their common tendon at the lower third of the tibial shaft. It passes through the tibial cartilage, overlaid by, but in close company with, the far more diminutive and narrower tendon of the flexor perforatus annularis primus pedis. When it arrives under the basal phalanx of the median toe, the outer one of the anterior pair, it bifureates to allow the other two flexor tendons to pass, while the slips thus formed become attached to the sides of the shaft of this joint close to its distal head. 32* 484 DR. R. W. SHUFELDT ON [Nov. 16, It will at once be seen that Geococcyx. californianus, in common with the vast majority of birds, has no special tendon devoted to the flexing of the second or prebasal phalanx of the fourth toe (here the reversed one). Provision is made for this in various ways in different birds. Here, in the subject before us, a special slip is thrown off for attachment from the deep flexor tendon as it passes over the prebasal joint in question, which slip virtually fulfils the function of a flexor perforatus annularis secundus pedis, did such a muscle with an independent tendon exist. The flexor perforans digitorum profundus (Plate XLV. fig. 2, S-p-p). This muscle is deep to all the flexors, and is situated directly on the posterior aspect of the tibia and fibula. It arises by two heads, one from the upper part of the tibia immediately below the overhanging rim of its summit, and the other, smaller, from the back of the head of the fibula. In the Corvide there is a well-developed third head, which comes off from above the fibular notch of the outer condyle of the femur, and in these birds, too, there is no fibular head to this muscle, but two tibial ones instead. Geococcyx agrees however, with most birds in having this muscle attached nearly the whole length of the posterior aspect of the shaft of the tibia by lightly attached carneous fibres. About a centimetre about the tibial cartilage it terminates in a strong subcompressed tendon, which, passing beneath the cartilage referred to, crosses the ankle-joint in front of all the other flexor tendons, and then passes through the inner of the two longitudinal perforations of the hypotarsal apophysis of the tarso-metatarsus. Down the posterior aspect of the shaft of this bone the tendon still maintains its anterior position and exhibits a predisposition to ossify. But this does not actually take place in the specimen before me. Above the distal trochlee, it makes the fibrous connection with the tendon of the flexor longus hallucis already described. This band is shown in the figure. Once within the limits of the post- trochlear space, the tendon of this muscle behaves in a manner common to most birds—that is, it quadrifureates, and each branch takes a course close up to the joints on their plantar aspects, and running through the slits in the perforated tendons pass in each case to the ends of the toes, where they become attached or in- serted upon the infero-proximal tubercles of the unequal phalanges. The one passing along under the fourth digit sends up a slip which is attached to the underside of the shaft of the prebasal joint, thus making good the deficiency here of what is represented in the other toes by an independent tendon. The tibial head of this muscle at its origin is directly covered by the soleus, while in the aperture existing between the two heads we can discern the popliteus. These flexor muscles, and others on both the front and rear of this limb, are moulded upon each other in a manner that can only be justly appreciated by a personal examination. In some the con- nections are quite feeble, the intervening tissue being easily separable, while in others the intimacy is very close, and great care is 1886.] GEOCOCCYX CALIFORNIANUS. 485 demanded on the part of the investigator to see that the separation is made along the proper divisions. I am convinced from my studies that a greater difference is to be found among the various muscles of birds than we have ever ac- credited them with, and this fact leads me to believe that the day will come when these differences can be called into play in taxon- omy with excellent effect. Perhaps if the myology of the leg is examined as carefully as Prof. Garrod examined the muscles of the thigh in this class, fully as many interesting and valuable distinctions will come to light. The popliteus (Plate XLV. fig. 2, popl) is quite well developed in Geococcyz, where it is seen to arise from an oblique line on the back of the tibial shaft below the head of the bone, and the fibres converging to pass upwards and outwards are inserted by a short tendon into the corresponding aspect of the head of the fibular, close to the superior fibres of insertion of the flexor perforans digitorum profundus. When engaged upon my dissections of the Corvide, recently I ascertained that this muscle was absent at least in the American forms of the group. This was also the case with the two peculiar muscles next to be described. The flezor brevis hallucis (Plate XLV. fig. 2, 7.6.2) is an exceed- ingly interesting little muscle, and one that it has not been my good fortune to have seen in birds before, as I have just said, nor can I find at band any description of it for this class by any previous anatomist. It arises from the side and the lower margin of the inner aspect of the hypotarsus of the tarso-metatarsus, and from some of the shaft of this bone immediately below. The fibres converge to terminate in a small tendon, which, passing down the postero-inter- nal aspect of the shaft, goes to the inner side of the basal joint of the hallux, about which it winds to finally become inserted on its underside, at the proximal extremity of this joint, just a little beyond its articulation with the tarso-metatarsal trochlea. Thus it will be seen that this little muscle is entirely devoted to assist in flexing the hallux. Its mesial fibres meet those of the muscle next to be described, down the mid-longitudinal line of the shaft of the bone which gives it origin. Equally engaging with the last is another still smaller muscle, the ewtensor brevis annularis (Plate XLV. fig. 2, #.6), on the opposite side of the same bone. Here we find its origin is much the same as for the flexor brevis hallucis, coming off from the external aspect of the hypotarsus and the shaft below. It soon terminates in an extremely delicate little tendon, which, passing directly down to the fourth or reversed toe, becomes inserted on the supero-inner aspect of the basal phalanx of this digit. By its contraction it will act as a direct extensor of this toe, a requirement no doubt made necessary through the feeble manner in which this digit is now served by the slip which goes to it from the common extensor of these phalanges. This tendon of the short extensor gets its leverage by the fascia which circularly binds down all the tendons of the flexors and 486 DR. R. W. SHUFELDT ON [Nov. 16, extensors, just above the sole on the one side, and which passes above the distal trochlez on the other. As we pass the muscles we have described for this limb in review, it will at once be recognized that the list is unusually complete. All the ordinary muscles of the thigh are present as found in birds, and all highly developed. In the leg marked specialization and organization are everywhere evident, while exceptional muscles are here, too, fully represented. This complexity by no means diminishes as we proceed towards the foot, for the arrangement of the tendons as they course down the tarso-metatarsus and the special musculature of this division of the limb is manifestly indicative of high organization. Finally, we have the complex insertional extremities of the intri- cate system above laid before us in the foot ; and the most exquisite examples of adaptation, compactness, and final requirements are to be seen throughout the structure on every hand. Notes on the Arterial System. Fortunately the evisceration that had been performed upon my specimen before it came into my hands has not injured the heart and great vessels. So by a careful dissection I am enabled to state that there are two carotids in Geococcyx californianus, and that their arrangement and the method of their branching at the base of the heart is normal. In other words, the bird in this respect is to be included with the Aves bicarotidine normales, as defined by Garrod. I would remark, however, that the carotids come off from the imnominates at points considerably further removed from the heart than that anatomist depicts them in his diagram of this condition. The branching is the same, however, and no doubt Mr. Garrod’s figures were intended to illustrate this point above all others, to which end they serve an excellent purpose. Turning to the arterial system in the pelvic limb, I find that the main artery of the leg is the sciatic. This agrees with the vast majority of birds, and, so far as I am aware, it is only in Centropus phasianus among the Cuculide that the rare condition of the femoral artery being the main one obtains. Of the Bursa Fabricii. As I said at the beginning of this memoir, Forbes has already called our attention to the peculiarity of form of this structure in the young of Geococcyx affinis (P.Z.S8. 1877, p. 312), and says that it completely disappears in the adult. I can verify this state- ment so far as the specimen before me is concerned, for in it this bursa is not present, while the region otherwise is characterized as we find it in the adults of the Centropodine. The Trachea. (Plate XLIII. figs. 3 and 4.) For the entire length of this subcylindrical tube, the osseous rings which compose it fail to meet in the longitudinal median line posteriorly. 1886.] GEOCOCCYX CALIFORNIANUS. 487 The interval thus formed, which is not very great, is occupied by a thin membrane which is continuous with the internal tympaniform membrane of the lower larynx. As to shape, the trachea diminishes in calibre gradually from above downwards, and nowhere in its con- tinuity does it present any enlargements or dilatations. This does not apply exactly to the bronchial bifurcations, for each one of them shows a disposition to swell just before arriving at the contracted parts of these tubes, where they impinge upon the lung- tissue. We may reckon either of these bifurcations as being partially sur- rounded by 13 semirings. Of course in this bird, as I say, the entire trachea may be regarded as having only semirings, but had the usual number of these united behind, there would still have remained the 13 semirings to each bronchial tube. An osseous pessulus is not present in Geococcyx, and the internal tympaniform membrane is quite extensive. There does not even seem to be any thickening of this membrane in our subject where this bony little bridge is located in those birds where it exists. As to its myology, the lower larynx is exceedingly simple in arrangement and meagrely supplied. Viewing the inferior part of the trachea and the bronchial tubes from in front, we can see but one pair of muscles, and these are the delicate sterno-tracheales. They are attached on either side to the last five tracheal rings (fig. 3, Plate XLIII.) ; the insertion seemingly consisting of two slips, the inferior one being attached to the lowermost of the five rings. These muscular slips soon merge with each other; and the muscle itself stretches across in the usual manner, for attachment to the inner surface of the costal process of the sternum. From a near view we discover another pair of muscles ; these are the tracheo-laterales (fig. 4, Plate XLIII.). They here extend the whole length of the tracheal tube, on its postero-lateral aspect, rather than fairly on its sides, as in the majority of birds. On either side they are carried down clear to the last bronchial semiring for attachment, a. e. not reckoning the aforesaid few semideveloped rings which we find at the terminal extremities of these bronchial bifurcations. This position of the tracheo-lateralis muscle is just the reverse of what Garrod found in such a bird as Opisthocomus (Scientif. Mem., p- 466, fig. 1) ; for, according to this authority, these muscles may be seen in the Hoatzin on an anterior view, and, moreover, in it they pass down in front of the sterno-trachealis. Garrod made many excellent examinations of the thoracic extremity of the trachea in the Gallinz, and among the representatives of this group an extraordinary variety of forms of this part of the bird’s economy was discovered (P. Z.S. 1879, p. 354). As the paper I refer to is profusely illustrated by drawings of the g!linaceous trachea, I have been enabled to compare them with the corresponding parts as I found them to exist in Geocoecyx. But of all the types given, I fail to find a single one that in any way resembles the subject before us. This is the less to be looked for, however, when we come to 488 DR. R. W. SHUFELDT ON [Nov. 16, consider how greatly the Gallinee differ among themselves in this part of their structure. So whatever affinities Geococcyw may have with this group, it is not evident in the form assumed by its trachea nor in the musculature of the lower larynx. Of the Tongue. My memoir upon the skeleton of this bird contains an illustration of the hyoid arches as they are found in it (Journ. of Anat., Jan. 1886, pl. viii. fig. 8), and here it will be of interest to show the form of the tongue itself. It will be seen from the figure of this organ (Plate XLIII. fig. 1) that its tip is rounded, and that its anterior moiety is ensheathed in a horny theea of a jet-black colour; the posterior half, however, is soft and fleshy, with its lateral margins fringed with delicate fleshy spines of a pure white colour and directed backwards. From above downwards it is somewhat compressed, while its form as a whole is that of an isosceles triangle the base of which is rather less than one third of a side, and which exhibits a deep angular notch. The lateral margins of the superior larynx are smooth and sharp, while its hinder edge supports a spine-like fringe, very similar to the one found on the borders of the posterior moiety of the tongue. Immediately back of this we observe the large and capacious entrance to the gullet, a feature which I have also included in my illustration of the parts under consideration. The delicate, backward-extending limbs of the hyoidean apparatus curve up but very slightly behind the cranium in this Ground- Cuckoo. Of the Ossiculum lacrymo-palatinum. Careful search was made for this ossicle in my specimen of Geococcyx, both orbits being included in the examination, but I am confident that no such bone is found in it. This bonelet was first described by Brandt, and is best seen in certain Albatrosses, and I have elsewhere described its location and appearance in Diomedea brachyura. According to Forbes, ‘it also occurs in forms so different from these as the Musophagide, many Cuculide, Chunga and Cariama, as well as in some Laridz and Alcide, so that its presence is obviously of no particular taxonomic value” (Coll. Mem. p. 415). It was this account of its occurrence in certain Cuculide that incited me to search for it in our present subject, but, as I have said, it does not possess it. In birds where it exists it is represented, when thoroughly ossified, by a delicate styliform bar connecting the descending limb of the lacrymal bone with the upper surface of the palatine. Conclusions. By the aid of the researches of Garrod and Forbes into the 1886. ] GEOCOCCYX CALIFORNIANUS. 489 structure of the Cuculidz and allied forms, together with the facts brought to light in the present article, we can arrange in a tabular form a number of the anatomical similarities and differences existing among Geococcyx californianus and the groups with which it is more or less nearly related; so that we may gain some idea as to its probable position in the system, at least as correctly as our present knowledge of its morphology seems to indicate. The group {S| slsls ce i Tendo n 5 : wi 43 ch pal or types & $ % B g 8 zg 4 : Oil of tensor Erey |r ey ot Wa & 2 ro} : os gland. .* . compared, alS|slElg 2 = x 3 patagii brevis, ) ‘ nde wo \ _- a dunt qrequey “SANVINYOATTVI XADI00039 40 ANOLYNY SI tise c 1886. | MR. R. LYDEKKER ON SCELIDOTHERIUM. 491 Prats XLY. Fig. 1. Outer aspect of the right pelvic limb of Geococeyx californianus showing the third layer of deep muscles, with a dissecting-chain pulling the ambiens into view. Life size, by the author from his own dis- sections. 2. Outer aspect of pelvis and right pelvic limb of Geococcyx californianus. Designed to show the deep muscles of the region, and the bones have been slightly rotated from their normal positions in order to bring them into view. «a. Vinculum between deep flexor and flexor longus hallucis. Drawn by the author from his own dissections. 3. Description of three Species of Scelidotherium. By R. Lyprexxer, B.A., F.G.S., F.Z.8., &e. [Received September 20, 1886.] (Plates XLVI.-XLIX.) In the ‘ Zoology of the Voyage of the Beagle,’ published in 1840, Prof. Sir Richard Owen founded the genus Scelidotherium on the evidence of a considerable portion of the skeleton of a large megatherioid Edentate found by Darwin in the Pleistocene of Bahia Blanca, in Patagonia, and applied the specific name of Jepto- cephalum. In the following year and in 1842, Lund published in the volumes of the Copenhagen Academy descriptions and figures of more or less imperfect remains of various allied animals from the Brazilian caves, all of which were eventually referred either to Owen’s genus or to the new genus Platyonyx, no less than seven new specific names being applied to these specimens. In 1850 the late Prof. P. Gervais published, in the results of Castelnau’s Voyage (‘ Mammiféres fossiles de Amérique méridionale’), a de- scription and figure of a skull from Buenos Ayres which he referred to the type species of Scelidotherium, and also of a second one from Tarija in Bolivia, which he did not name specifically but thought might be anew species. In 1857 Sir Richard Owen published a second memoir in the ‘Philosophical Transactions,’ in which he described and figured two skulls brought over in 1854 by Bravard from the Pleistocene of the Argentine Republic, both of which he referred to the type species. An important notice of the group was contributed by Dr. H. Burmeister, of Buenos Ayres, in his ‘Description Physique de la République Argentine’ ' (1879), where he described a skeleton which he likewise referred to the type species, and also gave reasons for adopting Lund’s genus Platyonyx for some of the allied forms. In 1880 Messrs. H. Gervais and Ameghino, in a memoir published under the title of ‘ Mammiféres fossiles de ’Amérique méridionale,’ gave a synopsis of all the previously named species of Scelidotherium and Platyonyx, and applied the new specific name of S. tarijense to the above-mentioned skull from Bolivia, figured by P. Gervais; and also founded a second * Vol. i. part iii, pp. 322-345, pl. xiv. There is no copy of the Atlas in any of the London libraries, 492 MR. R. LYDEKKER ON SCELIDOTHERIUM. [Nov. 16, new species, for which they proposed the name of S. capellini, on the evidence of a lower jaw from the Pleistocene of Buenos Ayres. In 1881 Dr. Burmeister published in the Monatsb. k. preuss. Ak. Wiss. (pp. 374-380) a description with figures of the manus, pes, and knee-joint of a skeleton of Scelidotherium from the Pleistocene of the Argentine Republic, which was referred to S. leptocephalum. In 1885 Dr. Fischer’ described a skeleton lately acquired by the Paris Museum of Natural History, which he refers to S. leptoce- phalum ; while in 1886 Sefior Ameghino* has applied the new name of Scelidotherium? bellulum to a single tooth from Parana. Finally it may be observed that the so-called Scelidotherium ankilosopum, Bravard’, is the same as Mylodon (Grypotherium) darwini, Owen. Other memoirs of minor import, which need not be quoted here, have also been published. It will be seen from the above that no less than eleven specific names have been applied to animals of this group ; six of which are included by Messrs. Gervais and Ameghino, in the memoir cited, in Scelidotherium, while four are referred to Platyonyx, the eleventh being of later date. Among the seven included under the former genus, there is no difficulty in regard to accepting the typical S. lep- tocephalum and S. tarijense ; S. capellini, however, as being founded on a specimen which has not yet been figured, must be regarded merely as a nominal species ; while S. minutum, Lund, is apparently founded upon immature specimens, and S. dellulum upon a single unfigured tooth. With regard to S. buchklandi and S. oweni of Lund, the type specimens are so imperfect that they do not appear to me to afford characters of sufficient importance to enable other specimens to be identified with them; and I have therefore been compelled to ignore these names when considering the affinities of the specimens described below. Of the four so-called species ranged by Messrs. Gervais and Ameghino under Platyonyz, the only one that can be regarded as satisfactory is P. brongniarti, which is founded on a nearly complete skull. P. euvieri is founded on a fragment of a mandible which does not afford more satisfactory characters than the one on which S. buchlandi is founded; while P. blainvillei and P. agassizi have been named on still more unsatisfactory evidence, and must certainly therefore be regarded as not of more than nominal value. The object of the present communication is, first, to show that one of the specimens figured by Sir Richard Owen in the memoir in the ‘ Philosophical Transactions,’ already cited, does not belong to S. leptocephalum, which also leads to the conclusion that the specimen described by Dr. Burmeister in his second memoir under the same name is likewise distinct ; and, secondly, to describe a skull belonging to a series of specimens, from the Pleistocene of Chili, recently acquired by the British Museum. In the course of this paper it will be shown that there appears no reason for the retention 1 Comptes Rendus, vol. ci. p. 1291 (1885). 2 Bol. Ac, Nac. Cordoba, vol. ix. p. 184 (1886). 3 In P. Gervais’s ‘Zool. et Pal. Générales,’ sér. i. p. 1382 (1867-69). 1886. ] MR. R. LYDEKKER ON SCELIDOTHERIUM. 493 of the so-called genus Platyonyx, which is either founded on a misidentification, or on characters which cannot be regarded as of more than specific value. With these few words of introduction, the descriptive portion of the memoir may be commenced. SCELIDOTHERIUM LEPTOCEPHALU M, Owen. The type species is represented in English collections by the imperfect type skeleton from Patagonia preserved in the Museum of the Royal College of Surgeons, and by two imperfect skeletons collected by Bravard in the Argentine Republic and preserved in the British Museum. The skull from the latter country, figured by P. Gervais in the ‘Mammiféres fossiles de Amérique méridionale ’ (Castelnau’s Voyage), pl. xi. fig. 1, apparently also belongs to this species. eThe type cranium is considerably damaged, but the two British- Museum erania (Nos. 37308 and 32995), taken together, exhibit nearly all the important features ; the second of these specimens is figured from the lateral aspect by Sir R. Owen in the ‘ Philosophical Transactions’ for 1857, pl. viil. fig. 1. In Plate XLVI. of the present memoir I have figured the former specimen, the occiput being restored from No. 32995. In the figured specimen the greater portion of the nasals is preserved, and its more important characters are as follows :— The facial profile is strongly curved, and presents a well-marked frontal protuberance behind the orbit ; the cranium is of moderate width, and the nasals of great relative length, being when complete at least equal to one half the total length of the frontal aspect of the cranium. In correlation with the elongated nasals the facial portion of the maxilla is lengthened, and a large portion of it appears on the frontal aspect. The lachrymal is not very promineut, and the aperture of its canal looks directly outwards. The anterior border of the zygomatic process of the maxilla is inclined backwards ; the fronto-parietal ridges are widely separated, and the interdental portion of the palate is not excessively narrow. The mandible associated with the figured cranium has an elongated symphysis, the portion in advance of the teeth being nearly twice the length of the whole dental series, and the superior border of the anterior portion of the ramus nearly straight. The more important measurements of the figured skull are as follows :— Length of broken nasals ............ 0°270 Length of facial part of maxilla ...... 0°170 Width of the two occipital condyles.... 0°108 Length from condyle to last tooth .... "242 Length of dental series; . ..06. 000.00 0113 Length of mandibular symphysis .... 0°156 Interval between hinder border of sym- physis and last tooth.. ........... 0°350 Interval between do, and first tooth.... 0°050 494 MR. R. LYDEKKER ON SCELIDOTHERIUM. [ Nov. 16, The only other part of the skeleton to which I wish to call attention is the astragalus, and I have accordingly figured the type specimen in Plate XLIX. fig. 3. It will be seen from this figure that the external trochlear ridge for articulation with the tibia is not prominent, and scarcely projects above the level of the internal tuberosity. The astragalus (B.M. No. 37476) associated with the cranium No. 37308 exhibits precisely similar features, although it is of somewhat larger dimensions. This type of astragalus is very widely different from that of Megatherium (in which the external trochlear ridge is extremely prominent), and apparently indicates that the eversion of the foot was not so great as in that genus. ScELIDOTHERIUM BRAVARDI, 0. Sp. This species is founded on an imperfect skeleton in the British Museum, brought by Bravard from the Argentine Republic, which presents features clearly showing that it cannot belong to the type species, to which it has hitherto been referred. The cranium (B.M. No. 37626), which lacks the whole of the dentition and the greater portion of the nasals, has been figured by Sir R. Owen in the ‘ Philo- sophical Transactions’ for 1857, pl. viii. fig. 2, from the palatal aspect *, and referred to the type species ; an upper view is given in Plate XLVII. of the present memoir. It is extremely unfortunate that the nasals are wanting ; but from the structure of the adjacent bones it can be shown that these bones were certainly much shorter than in S. leptocephalum, since in the first place the superior border of the facial portion of the maxilla forms a much shorter curve than in the latter, while if the nasals were of the same length as in that species they would have projected far in advance of the premaxille. That the nasals were of a shorter type is also evident from a com- parison of the figure with that of S. chiliense (Plate XLVIII.), when it will be seen that the facial portion of the maxilla is not dissimilar in the two species. The whole cranium is, moreover, relatively narrower than in S. leptocephalum, and the frontal profile is quite straight ; while only a narrow moiety of the facial portion of the maxilla appears on the frontal aspect ; and the lachrymal is charac- terized by its extreme prominence, and the partially upward direction of the aperture of its canal. The anterior border of the zygomatic process of the maxilla is nearly vertical, while the fronto-parietal ridges are closely approximated, and the interdental portion of the palate (as is well shown in Sir R. Owen’s figure) is of excessive narrowness. It will also be seen from the following table of dimen- sions that while the width of the occipital condyles is smaller than in S. leptocephalum, the interval between the condyles and the last tooth is considerably greater, which indicates a great difference in the relative proportions of the two crania. The premaxille are well developed. In the mandible * associated with the cranium, while the length of 1 The teeth have been introduced on one side in this figure. 2 This specimen is figured by Owen, op. eit. pl. viii. figs. 4, 5, with the teeth restored ; and apparently in pl. ix. figs. 2, 3, the specimen represented in fig. 2 being erroneously described as belonging to the upper jaw. 1886. ] MR. R. LYDEKKER ON SCELIDOTHERIUM. 495 the symphysis is greater than in S. leptocephalum, the interval between the hinder border of the symphysis and the first tooth is very considerably less. The superior border of that portion of the mandible in advance of the teeth is moreover inclined strongly upwards. The following dimensions may be compared with those of S. leptocephalum :— Length of facial part of maxilla (about) ....-.--- 0°135 Width of the two occipital condyles .........+.. 0°095 Length from condyle to last tooth...........+.- 0°258 Length of upper dental series ........-..++--: 0°105 Length of mandibular symphysis ............+: 0°175 Interval between hinder border of symphysis and BENNER, Fe wade BST bios io ryel har ney g SEE PHE DS 0°350 Interval between do. and first tooth ...........- 0°032 I will now direct attention to the astragalus. Unfortunately the one specimen of this bone, associated with the cranium, is imperfect, although sufficient remains to show that it differs from the corre- sponding bone of the type species by the great prominence of the external trochlear ridge, which projects far above the level of the internal tuberosity. In Plate XLIX. fig. 4, there is represented an astragalus from a cavern in Brazil, which, although of larger size than Bravard’s specimen, agrees precisely in structure, and either belongs to a male of the present form or to an allied species ; and I think a comparison of this figure with that of the astragalus of 8. leptocephalum will leave no doubt as to the specific distinctness of the two forms. This astragalus agrees precisely with the corre- sponding bone of a hind foot belonging to a perfect skeleton figured by Dr. Burmeister in the Monatsb. k. preuss. Ak. Wiss. for 1881, plate facing p. 380, fig. 2, and referred (on the authority of Sir R. Owen’s figure of the cranium of the present form) to a large male of S. leptocephalum. A tibia from Brazil, associated with the figured astragalus, presents a structure of its distal surface modified to accord with this peculiar articulation, which is different from that of the tibia of S. leptocephalum ; and there are equally well-marked differences in some of the other bones of the present form to which I shall allude on another occasion. Whether or no the larger bones mentioned above belong to male individuals of the same species as the cranium, I think sufficient evidence has been adduced to show that both the form to which the latter and that to which the former belonged are specifically distinct from S. leptocephalum. Confining, however, attention to Bravard’s specimen, it is quite evident that this form is distinct both from S. tarijense (in which the mandible is of quite a different type) and S. (Platyonyx) brong- niarti (in which the nasals are very short and the premaxille aborted) ; and since it appears impossible to identify it with either of the ill-defined Brazilian forms mentioned above to which specific names have been assigned, I propose that it should be known as 496 MR. R. LYDEKKER ON SCELIDOTHERIUM. __[Nov. 16, S. bravardi. Should, however, any of my fellow workers be able to identify it with either of such forms, I shall be only too happy to relegate this name to the rank of a synonym. The structure of the astragalus of S. bravardi (as Dr. Burmeister remarks in his description of the larger form which I provisionally associate) approximates very strongly to that of Megatherium, although wanting the articular cup for the navicular ; and it is there- fore probable that the hind foot of this species was more everted than in S. leptocephalum. ‘The shorter nasals of the present species also diverge less widely from the Megatherium type than do those of the last-named species, and this character is still more developed in the following form. ScELIDOTHERIUM CHILIENSE, Nl. Sp. The form to which I propose to apply the above name is repre- sented by a series of specimens purchased during the present year by the British Museum, from a gentleman residing at Lima, which were obtained from the Pleistocene of Tamarugal, in the district of Tarapaca in Chili’. The specimens comprise three more or less imperfect crania, the anterior portion of a mandible, and a consider- able number of vertebree and limb-bones. All that I have to say in regard to the limb-bones is, that the astragalus is intermediate in structure between that of S. leptocephalum and that of S. bravardi, and that the humerus has a well-defined entepicondylar foramen. The least imperfect of the three crania is represented in Plate XLVIII., and shows nearly the whole of the nasals. The most striking feature of this cranium is the extreme shortness and breadth of the latter bones—their length not exceeding one third of the total length of the cranium—while the mandibular symphysis is also equally short, as will be seen by the following measurements. That this form is totally distinct from S. leptocephalum is self-evident. It appears more nearly allied to S. dravardi, with which it agrees in the prominence of the lachrymal, the narrowness of that portion of the maxilla appearing on the frontal aspect, the straight facial profile, and the narrowness of the interdental portion of the palate; but differs by its greater width, by the still shorter facial portion, by the probable abortion (as will be shown below) of the premaxille, and by the shorter anterior portion and symphysis of the mandible. The mandible is quite unlike that of S. tarijense*, in which the symphysial part is bent upwards very suddenly, nearly the whole of it being above the level of the dental alveoli. The nasals of that species are also much longer than those of the present form. With the skull of the so-called Platyonyx brongniarti from Brazil, figured by Lund in the K. Danske Vid. Selsk. Skr. vol. ix. pl. XXvill., the present specimens agree very closely in general characters ; but in addition to being of superior size, the cranium is relatively narrower, and lacks the marked expansion behind the nasals, while 1 See map, supra, p. 396. * T refer to this species a left mandibular ramus from Brazil in the British Museum (No. 18649 a), 1886. ] MR, R. LYDEKKER ON SCELIDOTHERIUM, 497 the nasals themselves are more pointed posteriorly and wider anteriorly, the width of the anterior expansion being greater than that at the frontal expansion, while the reverse condition obtains in S. brongniarti. The resemblance between the two crania is, how- ever, sufficiently close to render it probable that the two forms were closely allied, and that the premaxille of the present form were cing aborted. The dimensions of the present form are as ollows :— Length of the facial portion of maxilla.......... 0°122 Width of the two occipital condyles ............ 0-099 Length from condyles to last tooth ............ 0'238 Length of upper dental series.................. 0:093 Length of mandibular symphysis .............. 0°124 Interval between hinder border of symphysis and BISCLUOGH, , o'er runes Sh eee ee 0°012 Since the present form is decidedly distinct from all the species mentioned above, and since I cannot identify it with either of the other ill-defined forms referred to Scelidotherium and Platyonyx,I can only adopt the course followed in the case of the preceding species ; and I accordingly propose to designate this form as Scelidotherium chiliense, since I shall immediately show that the genus Platyonyex ought to be merged.in Scelidotherium. Platyonyz is stated by Lund (and his view is followed by Dr. Burmeister’) to be distinguished from Scelidotherium by the absence of an entepicondylar foramen to the humerus, and by the more flattened phalangeals; while, according to Messrs. H. Gervais and Ameghino’*, the crochet of the last lower tooth is more prominent. Sir R. Owen*, who unites the two genera, is of opinion that the limb-bones referred by Lund to Platyonyx really belong to Glyptodon. I have no means of deciding which of these two views is correct ; but the close general resemblance in the structure of the nasals of Scelidotherium chiliense to those of the so-called Platyonyx brong- niarti leads me to conclude that whether the humerus of the latter was, or was not, provided with an entepicondylar foramen, the species is not entitled to generic distinction from Scelidotherium, the alleged differences in the structure of the phalangeals and of the last lower tooth being characters which are certainly not more than specific ones. Taking the three species, S. leptocephalum, 8. bravardi, and S. chiliense together, it will be seen that they form a sequence as here placed in regard to the length of the nasals—S. chiliense (together with S. drongniarti) being the least, and S. leptocephalum the most removed from the type of cranium obtaining in Mega- therium. Affinities of the Genus. In conclusion, I may observe that Scelidotherium appears to be a * Monatsb. k. preuss. Ak. Wiss, 1881, pp. 374-380. * ‘Mammiféres fossiles de l’ Amérique méridionale,’ p. 151 (1880). * Memoir on the Mylodon, p. 170, note. Proc. Zoou. Soc.—1886, No. XXXIII. 33 498 MR. R. LYPEKKER ON SCELIDOTHERIUM. _ [Nov. 16, genus occupying in some respects an intermediate position between Megatherium and Mylodon, but also showing evidence of a still more widely extended affinity. The dentition is decidedly nearest to that of Mylodon, while the hind foot approximates to that of Megatherium. The crania of species like S. chiliense and S. bravardi are those least removed from the Megatherium type, and it is these species which come nearest to that genus in the structure of the astragalus. All those forms in which the pes is known exhibit the anchylosis of the first and second phalangeals of the third digit, and the large claw of the same, which are such characteristic features of the type genus of the family. The peculiar Mylodon darwini (generically separated by Reinhardt under the name of Grypotherium) is the form by which Scelidotherium is connected by cranial characters with Mylodon ; and the connection is so close that it becomes somewhat difficult to give a clear differential diagnosis. In its extremely elongated facial region and peculiar astragalus, S. leptocephalum is the species departing most widely from the Mega- therium type, and it is probable, from the structure of the last-named bone, that in this animal the pes was not everted as it is in Mega- therium. In both its peculiar features S. leptocephalum makes such a very marked approach to the J/yrmecophagide, that it is quite easy to imagine how that family may have taken origin from some member of the Megatheriide ; while the remarkable resemblance in dental characters existing between those members of the genus Mylodon which have been separated by some writers under the names of Pseudolestodon and Lestodon and the Bradypodide suggests that the modern arboreai Sloths may also originally have sprung from some early member of the same great family of Ground- Sloths. EXPLANATION OF THE PLATES. Puate XLVI. Scelidotherium leptocephalum, Owen. Frontal aspect of the cranium; from the Argentine Republic. British Museum, No. 37308. The occiput has been restored from another specimen. 4. Ja, lachrymal; za, nasal; mz, maxilla. Pruate XLYII. Scelidotherium bravardi, Lydekker. Frontal aspect of the imperfect cranium ; from the Argentine Republic. British Museum, No. 37626. 4. Letters as in Plate XLVI. Prater XLVILII. Scelidotherium chiliense, Lydekker. Frontal aspect of the cranium, British Museum, No. M. 2819. 4. Letters as in Plate XLVI. Puatze XLIX, © Fig. 1. Scelidotherium bravardi, Lydekker, The mandible associated with the cranium figured in Plate XLVII. British Museum, No. 37649. 3. 2. Scelidotherium chiliense, Lydekker. The anterior part of the mandible; from Chili. British Museum. No. M. 2821. 3. 3. Scelidotherium leptocephalum, Owen. The left astragalus; from Pata- gonia. Mus. Roy. Coll. Surgeons, No. 3520. 4. a, external trochlear ridge for tibia ; 4, internal tuberosity. 4. (?) Scelidotherium bravardi, Lydekker. The left astragalus; from Brazil. British Museum, No. 186204, 43. Letters as in fig. 3. Fi iit © dio, WOOO. FL ALY La v3. Smib ith. Hanhart imp. SCELIDOTHERIUM LEPTOCEPHALUM. is . Ra 4229 : ) f he : — Ve Sea's = oan | ——- - > 14 < . ' : ~ \ v wl 1m art int | J. Smit lith P.Z.S. 1886.P1. XLVI. Hanhart imp SCELIDOTHERIUM CHILIENSE l 2 3 4 ») ‘od NN SCELIDOTHERIUM BRAVARDI CHILIENSE . LEPTOCEPHALUM. BRAVARDI Hanhart ump a2 1886.] | ON TWO EUROPEAN SPECIES OF BOMBINATOR. 499 4. On two European Species of Bombinator. By G. A. Boutencnr, F.Z.8. [Received September 28, 1886. ] (Plate L.) Two distinct forms of Bombinator occur in Germany. The fact has been known to me for many years, having, when a boy, been struck by the very different appearance of specimens obtained by me at Dresden as compared with the familiar form from Belgium and the Rhine. But it was only during a recent journey to Germany that I was enabled, by examining a larger material, to form a decisive opinion that the two forms are entitled to rank as species. German authors, so far as can be gathered from their publications, have never seized upon the distinction, although individual variations have caused a var. brevipes (Blasius), Koch, to be established. Possibly Fitzinger was the first to separate the two forms correctly by distinguishing a Bombinator pachypus, from the mountains of Italy, from the true B. igneus of Laurenti. However, perhaps through misrepresentation of Fitzinger’s views, nothing but confu- sion was added by Bonaparte, who, as is well known, introduced that author’s MS. name into nomenclature’. The result of my search into the synonymy of Bombinator is that Linnzus’s name Rana bombina and Laurenti’s Bufo igneus apply respectively to the two species now under consideration. ‘The words of Linnzeus (Faun. Suec. 2nd ed. p. 101, 1761), ‘* abdomine luteo nigro maculato,” and those of Laurenti (Syn. Rept. p. 29, 1768) “infra albido-cerulescens, punctatus maculis lete miniatis,” seem to settle the point ; and if, as I have reason to believe, the paler-bellied Frog occurs in Sweden and the brighter one in Austria, “‘ in paludibus Danubialibus,”’ it is settled - beyond doubt. Although Résel, as pree-Linnean and polynomialist, has no claim in matters of nomenclature, it is well to say that his, the first scientific, account of Bombinator refers to the form which I now name B. bombinus. It must also be added that B. pachypus and B. brevipes are undoubtedly to be regarded as synonyms of B. bom- binus, and that the sacrum and coccyx figured by Gené (Syn. Rept. Sard.) as that of B. igneus, and which has lately been the subject of some discussion, is clearly that of a Pelobates. I may now pass on to the distinctive characters of the two species. 1. Bomprnator Bomsinus, L. (Plate L. fig. 1.) Habit stouter, snout rather shorter, digits thicker, warts stronger and more crowded than in B. igneus. The length of the leg or crus equals or exceeds the distance between the inner metatarsal tubercle and the extremity of the fourth toe. Male with black nuptial exerescences under the second and third toes, sometimes also _ | Bonaparte’s figure was evidently not executed from life, and therefore no importance is to be attached to the coloration attributed to his B. pachypus, a 500 ON TWO EUROPEAN SPECIES OF BOMBINATOR. [Nov. 16, under the fourth ; without gular pouches, the submaxillary (mylo- hyoid) muscle being undivided. Upper surfaces without or with very indistinct dark spots. Young with a pair of roundish light spots or a light transverse band between the shoulders and another on the middle of the body; these spots often more or less easily distinguishable in the adult. Lower surfaces varying from sulphur- yellow to orange, with irregular blackish or bluish-grey spots or marblings ; the yellow colour usually predominates, and the blackish markings may even be entirely absent. Tips of fingers and toes yellow. Young very pale yellow inferiorly, with bluish-grey spots. Hab. I have myself collected this species in Belgium, where it is very abundant in the province of Namur, and occurs also near Tournay and Liége, in France near Bordeaux, in Rhenish Prussia, and in the Tyrol near Salzburg, where it is found in great abun- dance. 1 have at present before me living specimens from near Frankfort on the Main, kindly given to me by Dr. Boettger. Mr. W. Wolterstorff writes to me from Halle that this species is, in Germany, restricted to more hilly districts; he obtained it at ‘Tiefenort, near Kisenach, near Weismain and Muggendorf, between Bamberg and Baireuth, and round the Starberger See, near Munich. I have examined spirit-specimens from the following localities :— Hanover (Brit. Mus.), Goslar, Harz (Brit. and Berlin Mus.), Geneva (Brussels Mus.), Hungary (Brussels Mus.), Brostenii, Moldavia (Brussels Mus.), and Dalmatia (Brussels Mus.). For several speci- meus from San Romedio, S. Tyrol, and Marcellise, prov. Verona, I am indebted to the kindness of M. de Betta, and for two from Florence to Prof. Giglioli. 2. Bomprinator 1GneEvs, Laur. (Plate L. fig. 2.) The length of the leg is less than the distance between the inner metatarsal tubercle and the extremity of the fourth toe. No nuptial excrescences on the toes. In the male, the submaxillary muscle is divided into an anterior and a posterior portion, with a pouch on each side between the two ; this vocal pouch does not communicate with the mouth through any opening, but the skin of the floor of the mouth is loose and plicate, aud capable of distention during the inflation of the sides of the throat. Greyish or olive above, with distinct symmetrical blackish or bottle-green spots ; sometimes the whole or part of the upper surfaces washed with green; usually a pair of pale green roundish spots between the shoulders. Lower surfaces bluish black with white dots and briglit orange or vermilion insular spots ; tips of fingers and toes black. Young coloured like the adult. Hab. This species is common near Berlin, whence I obtained numerous specimens during a recent stay in that city. I also got it at Dresden, and I received some years ago specimens from Brostenii, Moldavia, together with B. dombinus ; these specimens are in the Brussels Museum, where I have recently compared them with the Berlin examples. Dr. Boettger received it from near Bitterfeld. Mr. Wolterstorff, who was so kind as to send me specimens from 25 IS Nei LUT jeam ao) 1886. ] ON THE ANATOMY OF THE TROCHILI, ETC. 501 Magdeburg, informs me that it is only found in the plain and never occurs in company with B. bombinus, which, however, may inhabit the same districts, but only at a certain altitude, as is, for instance, the case in Thuringia. Dimensions. B. bombinus. B. igneus, SS SS aoe. fe ae millim, millim. millim, millim, From snout to vent.. 46 46 46 42 ead eer as ee et 14 14 13 Width of head...... 15 15 15 11 Hore: limb!,..........-« 23 20 21 20 Eimaimb! ...... a0. 8o 51 52 48 hibias. Sec ete LG i) 14 13 Foot, from inner meta- tarsal tubercle .... 15 14 16 15*5 EXPLANATION OF PLATE L. Fig. 1. Bombinator bombinus. igneus. a. Adult female, upper view. 6, Adult female, lower view. e. Young, upper view. d. Young, lower view. e. Breeding male, lower view of foot. f. Breeding male, musculature of the throat. 5. Additional Notes upon the Anatomy of the Trochili, Capri- mulgi, and Cypselide. By R. W. Suurstpt, M.D. &e. [Received July 9, 1886.] To the meeting of this Society on December 1, 1885 *, I com- municated a paper on the “ Comparative Osteology of the Trochilidz, Caprimulgide, and Cypselidze,” wherein I ventured to bring forward certain anatomical facts in support of Professor Huxley’s expressed opinions upon the probable relations of the Humming-birds, Swallows, Swifts, and Nightjars (P. Z.S. 1867, p. 415). Although it does not in any way alter the general comparisons I made in my first contribution to this subject, nor my conclusions, et I find an unfortunate error has crept into the drawings of one of the Plates in the paper in question (plate lIxi. fig. 3). How this happened it would be impossible for me to say at the present time, but the humerus of Zrochilus alexandri in this figure is the right one, and not the left as stated in the text. It is quite possible that the extraordinary position of the pneumatic foramen in this bone, taken in connection with its diminutive size, or confusing the pair after the skeleton had been disarticulated for the purpose of studying the details, may have had something to do with the mistake, 1 See P. Z. 8. 1885, p. 886. 502 DR. R. W.SHUFELDT ON THE ANATOMY OF THE [Nov. 16, Fig. 2. Fig. A. rs Fig. 6 x Fig. 1. Anconal aspect of left humerus of Tuchycineta thalassina. X 3. Fig. 2. Palmar aspect of the bone shown in fig. 1. x 3. Fig. 3. Anconal aspect of the left humerus of Micropus melanoleucus. X 4. (This was the Panyptila saxatilis of my first paper, but I have now adopted the nomenclature of the A. O. U. for this White-throated Rock-Swift.) Fig, 4. Palmar aspect of the bone shown in fig. 3. x 4. Fig. 5. Anconal aspect of the left humerus of Trochilus alexandri. x 8. Fig. 6. Palmar aspect of the bone shown in fig. 5. x 8. By “anconal” I mean that side of the bone which is next to the body of the bird, and the reverse of this is the ‘‘palmar” aspect. All these figures are drawn from:the specimens by the author, and p.f. calls attention to the pneumatic fo sa. 1886. | TROCHILI, CAPRIMULGI, AND CYPSELIDE. 503 Be this as it may, the oversight has been kindly pointed out to me by Mr. F. A. Lucas, the osteologist of the United States National Museum, and it devolves upon me to set the matter right. The only changes it demands in the text of my article is, that on p- 908, in describing the humerus of T’rochilus, the sentence reading “but the radial crest is represented by a strong and gracefully curved hook”’ should state, instead of the “radial crest,” the udaar tuberosity. Again, in the description of this figure on p. 915, it should say the vight humerus instead of the left; and here as else- where in the paper take into consideration the changes that result therefrom. Nowas a correct comparison of these bones is of such high import- ance, and as I fully intend to carry my comparisons of the structure of these groups still further, I have redrawn, increasing in size and presenting two views, the humeri of the forms under discussion, and offer these drawings here as illustrations to the present article. From an examination of figures 1 and 2, it must be evident, to any one familiar with the ordinary form of the avian humerus, that in the Swallow the bone departs to some extent from the more common Shape it wears among the Passeres. The principal departure, however, consists in a marked shortening of the shaft, and perhaps a comparatively more conspicuous radial crest. The bone is likewise non-pneumatic. This also we find to be the case in the Swift, where, too, the radial crest is drawn out into an upturned hook, and the ulnar tuberosity is simply drawn out further and consequently more hook-like. Now turning to the Humming-bird (figs. 5 and 6), we find a humerus that, so far as my knowledge extends, has not its counter- part among living birds. In the first place, the extraordinary position of its pneumatic fossa, being on the radial side of the bone, is an exception to every general definition of a bird’s humerus that the writer has ever met with. Of the peculiar method of insertion of the pectoralis major muscle in this bird I shall have something to say in a future contribution. As will be seen from the figures, the ulnar tuberosity is a prominent decurved process, and one of the most striking features of this curiously twisted bone. It would be superfluous on my part to point out in the figures the manifest differences existing between the humerus of this Hummer and the Swift; they are even greater than I thought them to be, before I made the oversight above quoted. In addition to its general form, the humerus is highly pneumatic in Zrochilus, which, as I have said, is not the case among the Cypselide, these latter agreeing with the Swallows in this particular in having non-pneumatie humeri. 504 ON ANTELOPES FROM SOMALI-LAND. [Nov. 16, 6. On two Species of Antelopes from Somali-Land. By P. L. Scuater, M.A., Ph.D., F.R.S., Secretary to the Society. [Received September 20, 1886.] (Plate LI.) In Mr. E. Lort Phillips’s ‘‘ Notes on the Antelopes of Somali-Land” (P. Z.S. 1885, p. 930) is mentioned a Gazelle under the name of “ Flabby-nosed Gazelle,” the single specimen of which, in deter- mining Mr. Lort Phillips’s species, I reserved for future examination. I was in hopes of being able to have the bones removed from the head of the single specimen obtained, in order to ascertain whether there is not some peculiarity in the frontal and nasal bones to accompany the extraordinary developinent of the nose in this animal. Not having been able to obtain the necessary facilities for this purpose (which, seeing that the specimen is unique and has been excellently mounted, was not much to be wondered at), I will content myself with again exhibiting the head of this remarkable Antelope (Plate LI.), and remarking that I think there can be no question of its belonging to an undescribed species, which I propose to call Gazella naso. Gazella naso, as its name implies, is sufficiently distinguishable from all other known members of the genus by having the extremity of the snout above the nasal openings developed into a large flabby wrinkled mass, which is scantily covered by short hairs of a grey colour. Above this elevated mass the face is crossed by a broad black bar. Above that again the centre of the forehead and space between the horns is covered by dense fur of a chestnut-red colour. This chestnut-red forehead is bordered on each side by two broad white longitudinal stripes, which extend from the base of the horns down to the nostrils. This longitudinal stripe is again bordered above the eye on the inside to below the eye on the outside by an indistinct blackish stripe. The tear-pits below the eye seem to be particularly large and well developed. The rest of the fur of the head and neck is of the sandy colour usual in most species of this genus. The ears, which are long and rather narrow, are of a greyish colour. In the size and shape of its horns G. naso does not differ materially from other species of the group allied to G. dorcas. The length of the horns in the present specimen, from the base to the tip, is about 93 inches; the breadth of the skull between the eyes is 1*7 inch; the length from the occiput to the end of the nose about 8 inches; the length of the ear is 6 inches. As regards the Neotragus, of which specimens were obtained by Mr. Phillips and were likewise left undetermined in the same com- munication (see P. Z.S. 1885, p. 932), I have now compared the skull and the skin brought by Mr. Phillips with specimens in the British Museum. As regards the skin there is such variation in the coloration of the fur of Neotragus that I do not think much reliance can be placed on the somewhat abnormal appearance of this _ - 1886.] ON THE STRUCTURE OF THE OVUM IN DIPNOI. 505 example, which is nearly paralleled by other specimens in the National Collection. ‘The skull, however, is characterized by the excessive reduction of the nasal bones, which is carried to a much greater extreme than in the typical specimen of Neotragus kirkii, Giinther (P. Z. S. 1880, p. 20). There are also other points of difference when the skulls are compared together. But as Neotragus kirkii is from nearly the same country, I think it would be hardly justifiable to name a second Neotragus from Somali-Land without a better series of materials to base it upon. I will therefore content myself with calling attention to their diver- gencies, and, as Mr. Phillips has empowered me so to do, with depositing his specimens in the British Museum to await further inquiries. From the discoveries made by Mr. Hagenbeck’s collector, Herr Menges’, and Messrs. James and Lort Phillips, it is quite evident that there is yet much interesting work to be done among the Mammalia in Somali-Land, and I trust that we shall soon receive additional specimens and further information concerning this inter- esting animal. December 7, 1886. Prof. Flower, LL.D., V.P.R.S., President, in the Chair. Prof, Bell exhibited and made some remarks on a specimen of Tenia fana, the smallest known human parasite, which had lately been obtained for the Museum of King’s College. The following papers were read :— 1. Observations on the Development and Structure of the Ovum in the Dipnoi. By Frank H. Bepparp, M.A., F.R.S.E., Prosector to the Society, and Lecturer on Biology at Guy’s Hospital. [Received December 3, 1886.] (Plates LII.—LIV.) The present paper is the continuation of a research into the structure of the ovary in Protopterus, the main results of which have already appeared in the last number of the ‘ Proceedings.’ Besides being able to give a more complete account of the ovarian ova in Pro- topterus, I am also able to supplement this account with some few notes respecting the structures to be observed in the ovary of Cera- todus. ‘The opportunity of studying Ceratodus 1 owe to the kindness of Prof. Lankester and Prof. G. B. Howes. ‘The material was taken * Cf. Sclater, P. Z. 8. 1884, p. 538; Noack, Zool. Gart. xxvi. p. 172 et xxvii, p- 39; Kohl, Ann. d. k. k, naturhist. Hofmuseums, i. p. 75 (1886). ow} 506 MR. F. E, BEDDARD ON THE DEVELOPMENT AND [Dee. 7, from fishes which had been preserved entire in alcohol, and was unfortunately not in a very first-rate condition for microscopical investigation. I have been able, however, to make out the important fact that there is an essential similarity in the structure of the ovarian ova in both forms, and that in Ceratodus, as in Protopterus, there are, besides the ova, certain other structures resembling ova in many particulars which have a different mode of development. The discovery of this fact in Ceratodus renders it practically impossible to suppose that the remarkable processes in the development of the germinal cells of Protopterus, described and figured by myself in this and my last paper, are in any way abnor- mal; it had occurred to me before that there might be something abnormal. It cost me a great deal of labour, in the way of cutting sections, to ascertain that there was an actual resemblance between Ceratodus and Protopterus. In my specimen of Protopterus I found it quite impossible to make a section of the ovary anywhere without dis- covering ova of both kinds in nearly equal abundance ; in Ceratodus, on the other hand (and this statement applies to two specimens), ova of the second kind were extremely rare; I have cut literally hundreds of sections without coming across any evidence of the existence of two kinds of ova. This may be a real difference between the two genera, or may depend upon the season of the year at which the specimens were captured. In every case, however, the ovaries contained numerous mature ova, though the number of these latter was very much less than that of the immature ova. On the other hand, it is possible that there is really a difference in this respect between Protopterus and Ceratodus, which show other important anatomical differences. I have already contributed to the ‘Zoologischer Anzeiger’ (No. 236) a brief note of the principal facts contained in this paper. I have but little to add to my former paper on the structure of the ordinary ova of Protopterus. In my last paper I drew attention to the curious specialization of the yolk in the adult ova; in fig. 4 of plate xxviii. of that paper is illustrated an adult ovum which shows a differentiation of the yolk into two distinct layers, which are less distinguishable by their coloration or arrangement of yolk-particles than by the very definite break which separates them. ‘he outer layer of yolk forms a com- paratively thin envelope, the greater portion of the ovum being occupied by the central mass of yolk. Van Bambeke’ has recently noted and figured a similar condition of the ripe ovum in Godius niger and other fishes, and Pfliiger had previously referred to the same phenomenon in Mammalia. Ac- cording to Van Bambeke, the distinction between the two zones occasionally disappears under the influence of reagents. Van Bam- beke speaks of the line of division which separates the two zones as not being a membrane, but merely a condensation of the egg- protoplasm. With this opinion I fully agree: in the first place, the 1 Arch. d. Biol. t. iv. (1885). 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOI. 507 division of the ovum itself into two zones by a definite membrane would seem to be an absurdity; in the second place, no membrane was evident in preparations where the ovum was broken. It might be expected that when the ovum was broken in cutting, the membrane, being presumably of a different hardness to the egg-protoplasm, would project from the cut surface ; in no instance, however, did the broken surface show any indication anywhere of a membrane. The line of division between the two yolk-zones presented the appearance in my preparations of an absolute break ; the protoplasm was perfectly transparent, and, being unaffected by the staining- reagent, was invisible. I did not notice this differentiation of the yolk in all the large ova visible in my sections. In some ova, which were full of yolk, and of equal size with those just referred to, there was no trace of any such specialization into a peripheral and central zone; in these cases the yolk was uniform throughout. Such ova were to be found not only in the same ovary, but in the same section with the ova which dis- played a differentiation of the yolk. This circumstance renders it improbable that the effect of reagents has caused the yolk to acquire a uniform appearance. A comparison of the two kinds of ova has led me to the conclusion that the ova in which there is a specialization of the yolk are nearly mature, while those in which the yolk is uniform are degenerating ova. Another matter relates to the structure of ege-membranes and their homologies, where I have to make a correction. In my former paper I have referred to the presence in compara- tively young ova of a vertically striate membrane lying within the vitelline membrane (loc. cit. p. 273, pl. xxviii. fig. 1, 2.7; pl. xxix. fig. 2, 2.7). This, it now appears to me, is not the equivalent of the inner of the two membranes which surround the Teleostean ovum’. The early disappearance of this membrane and its general structure granular and with no distinct line of separation from the subjacent egg-protoplasm) were against such an interpretation ; I now identify it with more confidence with a specialized layer of the egg-protoplasm described by Brock in Alburnus lucidus, Salmo fario, and Perca fluviatilis, and by Owsiannikow in Acerina vulgaris. Brock has figured this layer (the ‘‘ Zonoidschicht”’ of His, the “helle Rand- schicht”’ of Gegenbaur) in Alburnus lucidus (Morph. Jahrb. Band iv. pl. xxviii. fig. 12, fg.), where it is more complicated than in Lepido- siren and consists of two layers—an inner homogeneous and an outer vertically striate layer. ConTENTS OF THE OvARyY OF PROTOPTERUS. The following is a detailed account of the structure and develop- ment of certain bodies in the ovary which have already been partly described in my former paper; they are nearly as numerous as the ordinary ova. 1 Of.J. T. Cunningham, “ On the Mode of Attachment of the Ovum of Osmerus perlanus,” P.Z.S. 1886, pt. iii. p. 292, pl. xxx. fig. 4, z.7.i, and other memoirs. 508 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [Dec. 7, Stage 1.—The earliest stage of these bodies is represented in fig. 1; its different constituents are figured, highly magnified, in figs. 5, 14—20. The whole structure is situated near to the surface of the ovary, with which indeed it is still in continuity ; the germinal epithelium (ge), which is apparently not everywhere present as an external layer in the adult ovary, is here conspicuous by its presence; it forms a mass of cells, the nuclei of which are so large and so closely pressed together that I have found it impossible to detect any cell-outlines (see fig. 1). These thickly clustered groups of epithelial cells seem to correspond to the “epithelial islands ” of many writers (see Iwakawa, G.J.M.S. 1882, p. 266). The nuclei of these cells are deeply stained by borax carmine, and for the most part rounded or oval in contour, though frequently (perhaps owing to the hardening-reagent) some- what angular. The staining-fluid is not evenly taken up by the whole nucleus, but a peripheral layer, sometimes confined to one pole of the nucleus, is very deeply stained, the central regions being compa- ratively pale. The germinal epithelium is immediately continuous with a mass of cells which form a hollow sphere, partly occupied by a plug of cells of a somewhat different appearance ; the spherical mass of cells is quite close to the surface and connected with the germinal epithelium by a very short neck, which is as wide as the area occupied by the patch of germinal epithelium. The peripheral mass of cells is already differentiated into two distinct layers, which are distinguishable from each other by the characters of the component cells and more particularly of their nuclei. The outermost layer is of course the one that is in contact with the germinal epithelium ; the outlines of its cells are not very visible in my preparations: between the nuclei of the cells is a fibrous substance moderately stained by borax carmine; this appears to me to be the slightly altered protoplasm of the germinal cells themselves, and not to be an inroad of connective-tissue stroma-cells. The germinal cells bear, however, a very striking resemblance to connective-tissue cells. Balfour has figured (Q. J. M.S. 1878, pl. xvii. fig. 10) and described (p. 390) a condition of the Elasmobranch ovary which is so far very similar to that which I have just described, and which gives me greater confidence in stating that the cells displayed in fig. 1, fé, of Plate LII. are really germinal and not stroma-cells. He says (p. 391) :—‘*The surface of the ovarian region .. . is covered by a distinct ... pseado-epithelium ... The cells of the pseudo-epithelium have one peculiarity very unlike that of ordinary epithelial cells. Their inner extremities are prolonged into fibrous processes which enter the subjacent tissue, and, bending nearly parallel to the surface of the ovary, assist in forming the tunic spoken of above. This peculiarity of the pseudo-epithelial cells seems to indicate that they do not essentially differ from cells which have the character of undoubted connective-tissue cells, and renders 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOI. 509 it possible that the greater part of the tunic, which has apparently the structure of ordinary connective tissue, is in reality derived from the original germinal epithelium, a view which tallies with the fact that in some instances the cells of the tunic appear as if about to assist in forming the follicular epithelium of some of the developing ova.” The nuclei of the peripheral layer of cells are much like those of the proliferating germinal epithelium, though not quite so darkly stained—perhaps for mechanical reasons. Their shape varies con- siderably, some being rounded and some more fusiform; but these two extremes are united by numerous intermediate conditions. For the most part the nuclei have taken up the staining-fluid unequally ; a patch at one extreme of the nucleus is more darkly coloured, and from this radiate slender threads towards the opposite extreme of the nucleus ; the interstitial part of the nucleus is stained of a pale pink. The different forms of these nuclei are represented in fig. 5. The differential staining of the nucleus undoubtedly corresponds to the differentiation of its substance ; and the star-like form of the darkly staining part suggests a connection with the phenomena of nuclear division ; but I have not observed any cases in which the ceatres of the star-like bodies in two adjacent nuclei were opposed; in every instance the darkly stained extremity of the nucleus was directed away from the germinal epithelium and along the axis of the layer of cells; this uniformity in the nuclei gives them the appearance of being in rapid motion, of being as it were swept along by a current round the periphery of the sphere of cells. Here and there the continuity of the layer of cells is interrupted by blood-vessels (4.2), usually of small dimensions, which are the fore- runners of the richly developed vascular supply of these same bodies in later stages of development. The appearance of blood-vessels was more common on that side furthest from the germinal layer than on that nearest to it. Towards the opposite extremity of the sphere of cells, ¢. e. that furthest removed from the outside of the ovary, the character of the nuclei of the peripheral layer of cells becomes changed. In this region the nuclei have lost the peculiar arrangement of the nuclear substance and-present the appearance of ordinary nuclei (fig. 5a) ; that is to say, they are oval bodies with finely granular contents and here and there round, darkly stained particles which are disseminated throughout the nucleus. Within the peripheral layer of cells is another layer of cells which becomes ultimately comparable to a follicular epithelium, Even in this early stage of development it is for the most part distinguishable from the outer layer of cells; the distinction is not only in the character of the cells and their nuclei, but in an absolute line of demarcation which separates the two layers; this consists (fig. 1, x) of a narrow band of structureless substance, which bears the closest possible resemblance to a substance produced by the fusion of some of the central cells of the sphere, and which will be described shortly, It is possibly formed by a metamorphosis of the peripheral layer of 510 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [ Dec. 7, the follicular cells, but serves at any rate to determine accurately the boundary line between the follicular layer proper and the mass of peripheral cells which ultimately bear a resemblance to the secondary follicle layer. This limiting band of structureless substance is only met with on that side of the cell-mass towards the outside of the ovary ; elsewhere the cells of the follicular epithelium are perfectly continuous with the cells of the peripheral layer. The nature of the cells of the follicular layer also differs from that of the more peripherally placed cells. The cells themselves are rather larger and irregularly rounded in form ; there is no trace of the con- nective-tissue-like structure described above, in the case of the extra- follicular cells. The cell-contents are clear and for the most part hardly affected by the staining-agent, which has coloured their nuclei deeply ; the part of the cell-protoplasm that is coloured is tinged very faintly and shows a reticulate arrangement. The nuclei of the folli- cular cells differ for the most part from those of the extra-follicular layer by being rounded and even in shape, and all closely similar in size; they are deeply stained, and show a tendency to the same reticulate arrangement of the nuclear substance that has already been mentioned in the extra-follicular cells. The character of this follicular layer is much the same through- out, only differing in places by the more or less crowded condition of the nuclei, indicating a more or less active multiplication of the cells. On that side of the cellular mass which is furthest from the outside of the ovary, the follicular layer comes into closer relations with the extra-follicular epithelial layer, though still recognizable. The character of the cells and of the nuclei which make up the extra- follicular coat of cells alters, and every transitional condition is met with between these cells and the cells of the follicular epithelium. This seems to indicate that the follicular layer is formed as a differentiation of the mass of invaginated germiual cells. The whole body is thus surrounded by three distinct and inde- pendent layers—(1) the single layer of large follicular cells; (2) a vascular layer, to which reference has already been made and which is extremely developed ; (3) an outermost cellular layer, consisting of flattened cells with nuclei elongated in the direction of the cireum- ference of the ovum; this layer, like the follicular layer, is only one cell thick. For the most part this outer layer has been neglected by writers, or else has been confused with the true follicular layer. Balfour, however, has recognized it in the Elasmobranch ovum* and has proposed to call it the ‘‘ secondary follicle-layer.’ Owsiannikow figures this layer in the ovum of the Perch*; in the explanation of the figure it is called the follicular layer, while the true follicular cells are termed the “granulosa”’ ; in the text of his paper, however, the term endothelium is constantly used for this layer, which is stated to be made up of several rows of cells in many fishes. Concerning the origin of this layer Balfour expresses with hesitation 1 Quart. Journ. Mier. Sci. vol. xviii. (1878), p. 405, pl. xix. fig. 29, fe’. 2 Mém. Acad. Sci. St. Pétershourg, t. xxxiii. (1885) no. 4, pl. 1. fig. 4, a. 1885. | STRUCTURE OF THE OVUM IN THE DIPNOI. 511 the opinion that it may be derived from the germinal epithelium. Owsiannikow suggests three possibilities either it originates from cells which have made their way out of the blood-vessels (!), or from cells of the subgerminal tissue (stroma ?), or, finally, they may be derived from the germinal layer. The latter alternative is adopted by Owsiannikow on certain evidence, which he does not, however, regard as conclusive. The outermost follicular layer of Lepidosiren I have already (p. 509) shown without doubt to be derived from the germinal epithelium; I shall therefore adopt the name of secondary follicular epithelium for this capsule, which indicates that its origin is similar to that of the true follicular epithelium, which may be briefly termed the follicular epithelium. The two layers that have just been described form a hollow sphere enclosing a central cavity, which is partly occupied by a mass of cells. It is very possible that in the fresh condition the central mass of cells occupies the whole of the space available, but this is not the case in my preparation. A large portion of the central cavity, particularly on the side turned towards the exterior of the ovary, is quite empty, and no structures intervene between the central mass of cells and the follicular layer. On the opposite side, however, the central mass is in close contact for a con- siderable area with the follicular cells, this area exactly corre- sponding with the transitional area between the follicular and external layers. These facts would suggest that the central cells are derived from the proliferation of the follicular cells and ultimately of the extra-follicular cells, as these two latter have been shown to be perfectly continuous, the proliferation taking place in a certain limited area only. In this case the apparent cavity which separates the central cells from the follicular on one side will be an indication (exaggerated by the action of the preservative reagent) that there is here no real connection between the central and peripheral layers, though they may be in actual contact in the fresh state. A number of the central cells are displayed in figs. 14—20 of Plate LIII.; they are more or less irregular in shape, rounded, and of different sizes; the staining-reagent has hardly affected the cell- protoplasm, but has deeply stained the nucleus. The cell-protoplasm is arranged in a reticulate fashion, and closely resembles that of the follicular cells. Some of the cells contain two or more nuclei, which seems to show that the cells themselves are in a condition of multi- plication. The most remarkable fact about the nuclei of the central plug of cells is their great inequality in size: some of the variations are exhibited in those figures ; the variation is all the more remarkable as it does not occur in the follicular layer, the nuclei of whose cells are of quite a uniform size. There is almost every gradation in size between the smallest and largest nuclei, a fact which perhaps indicates that the smaller ones are the result of nuclear division. The largest nuclei rather excel in size those of the follicular epithelium. There is a similar difference of size in the peripberal layer of cells, particularly obvious at those points where the peripheral layer is in 1 Loe, cit. p. 30. BZ MR. F. E. BEDDARD ON THE DEVELOPMENT AND [Dec. 7, contact with the interior mass of cells, the follicular layer being at such points indistinguishable. It is possible that the difference of size in the nuclei corresponds to a distinction between “ primitive ova” and “ germinal cells”? such as has been described by Semper, Balfour, and so many writers in other Vertebrata ; in this case the larger nuclei will be the primitive ova. This suggestion must be of course only regarded as such; I have no real evidence to offer except the different size of the nuclei. In very many instances a degeneration of the nuclei could be observed. This takes place in several ways, some of which may be stages in the same series. Some of the nuclei (figs. 14,17) remain of the same size and shape as the normal nuclei, but show a much paler colour and fewer nucleoli ; in one instance (fig. 15) I observed a commencing disintegration of the nucleus, the substance of which appeared to be in a condition of solution at one point where it passed gradually into the substance of the cell, the limiting membrane of the nucleus being here invisible. In other cases (figs. 19, 20) the nuclei are as darkly stained as the normal nuclei or even rather more so, but instead of presenting a uniform oval contour, the nucleus was variously contorted and irregular in shape. The centre of the mass, however, is not entirely occupied by cells like those that have just been described. There is a certain amount of an amorphous substance (fig. 1, p), well stained with the borax carmine, which lies in patches between some of the central cells, and particularly on the outside, in the space which separates them from the follicular layer. This substance is of an homogeneous appear- ance, though lighter in colour in some regions than in others ; it is rather more abundantly developed in the stage next to be described than in the present (cf. fig. 9, Plate LIII.). This substance encloses patches of cells, or sometimes single cells; occasionally the proto- plasm of the cells has undergone a certain change at the periphery, where it gradually passes into the homogeneous mass surrounding it ; frequently scattered nuclei are to be found imbedded in it, and a comparison of these nuclei with those of the central cells shows them to be identical. The general appearance of the homogeneous substance suggests a coagulated fluid, and it is very like the liquor folliculi of the Mammalian ovum coagulated by alcohol; but this substance cannot be excreted by the central cells or by the follicular cells, because it contains numerous traces of them in the shape of free nuclei with or without a certain amount of partially altered protoplasm attached. These facts rather indicate that the sub- stance in question is produced by the alteration and fusion into a semifluid mass of some of the central cells. This mode of formation is, however, not opposed to a comparison with the Mammalian liquor folliculi, which has been asserted by some to have a similar origin ; the great difference is that this semifluid substance has the power of forming yolk, as will be seen after the description of the later stages. There are other bodies which seem to be referable to the stage just described, though differing in certain structural particulars as well as in their smaller size. 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOI. 513 These, like the last, are connected with the germinal epithelium, covering the outside of the ovary, by a pedicle of epithelial cells, which is nearly of the same width as the whole structure and its follicle. The germinal epithelium is in a condition of very active multiplication, the nuclei being very closely crowded together. The layers of cells which surround the central mass cannot be differentiated ; they present the appearance of a mass of cells con- tinuous with the germinal epithelium and forming a layer of cells three or four deep ; only here and there (fig. 10, 5/) were traces of the irruption of the stroma in the shape of small blood-capillaries. The cells which constitute this peripheral layer are precisely similar in their character to the cells which form the outermost of the peripheral layers in Stage I. In two instances belonging to this stage, which I have been able to study, the homogeneous darkly-staining mass produced by the solution and fusion (?) of the protoplasm of the central cells was much more in amount than in the last described stage. Fig. 11 of Plate LIII. represents the central mass of cells, which are seen to be divided up into partly or entirely isolated clumps by the formation of this homogeneous mass, which contains also free nuclei (fig. 11, 2). In the third case the condition of the central cells, so far as this fused mass of protoplasmic material is concerned, was much the same as in Stage I. On the whole these facts appear to indicate that the bodies belong to a somewhat earlier stage than those just described and shown in fig. 1 of Plate LII. Their small size, the undifferentiated condition of the peripheral layers, as well as the very small amount of stroma (blood-vessels) between the cells of these layers, appear to me to point to this conclusion. On the other hand, the greater amount of change in the central cells, z. e. the inereased amount of the deeply- staining fluid substance between isolated clumps of cells, is against such a supposition, as it is evidently a further development of a process which has only just commenced in the developing structure which J have last described. This latter reason is perhaps not a very powerful argument, because it may easily be supposed that the pro- duction of the semifluid protoplasmic substance may be hastened or retarded ; the same may be said with regard to the specialization of the follicular layers, only that a specialization in the instances observe! by myself goes together with increase of size of the whole body. Accordingly I am inclined to believe that the bodies displayed in fig. 9 of Plate LIII. belong to a younger stage than those illustrated in fig. 1 of Plate LIL. Stage 11.—The different layers composing the foliicle are more differentiated, and each individual layer is now quite recognizable, Commencing from the outside, we have the secondary follicular layer, between which and the follicular layer proper is a well differentiated vascular layer, which is easily to be made out through the whole circumference ; the blood-vessels are filled with blood, and appear as round, elliptical, or elongated according to the angle of the section. The follicular layer has the appearance of being only Proc. Zoou. Soc.—1886, No. XXXIV. 34 514 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [ Dec. 7, one cell thick, but the nuclei of its constituent cells are so crowded together that it is not easy to be certain upon this point. The- outlines of the follicular cells are in many places plainly visible, and irregular processes (Plate LIII. fig. 6) project from these cells toward the interior of the mass. This may very well be owing to the shrinking of the central mass of cells, and the consequent breaking away of its connection with the peripheral epithelium. A comparison of the complete series of sections through the developing ovum (the section fig. 6 is towards the middle of the series) shows that, whether or not there is a connection between the entire periphery of the central cells and the follicular epithelium, there certainly is such a connection throughout a limited area lying on that side of the ovum which is nearest the external surface of the ovary, a little above (or below) the pedicle which unites the germinal epithelium with the ovum. In this region the nuclei were more abundant and crowded together than in the central cells of the mass, and were of uniform size and rounded form ; in fact they show an exact similarity to the nuclei of the follicular epithelium, which in this stage, as already mentioned, forms a distinct layer. The mass of cells which connects the follicular layer with the central cells is therefore closely similar to the follicular layer, and has the appearance of a proliferation and growth inwards of that layer. The central cells, as in the previous stage, have nuclei of varying size ; some are long and oval, and others shorter and more spherical ; the latter resemble in every particular the nuclei of the surrounding follicular layer. A characteristic feature of this stage is the commencing formation of yolk, which is visible here and there (figs. 27-31) in the cells of the central mass, and in the form of droplets of homogeneous appearance and varying size. ‘This formation of yolk is not confined to the central cells, but is recognizable also in the cells which make up the follicular layer. Here and there among the central cells are homogeneous masses, evidently the same as those referred to in the description of Stage I. as a probable resultant of the breaking-down and fusion of certain of the central cells. These masses were, however, much less developed than in the earlier stage. This stage is evidently, from the facts above narrated, in a further condition of development than that which I have termed Stage I. ; this is also shown in the gradually-advancing separation of the peri- pheral layers from the germinal epithelium of the ovary. In the earlier stage the pedicle which unites the epithelial layers with the germinal epithelium on the surface of the ovary is not only very thick, but composed almost entirely of germinal epithelial cells in a state of active multiplication. The stroma of the ovary had barely penetrated into this mass of invaginated germinal cells. In Stage II. the body is just as near to the surface of the ovary, and there is a shallow depression on the surface of the ovary corre- sponding in position to the centre of the pedicle of attachment, which would appear to be the remains of the invagination of the germinal epithelium. The activity of the germinal epithelium has, however, 1886.] STRUCTURE OF THE OVUM IN THE DIPNOI. 515 greatly diminished ; it forms only a single layer of cells, and the pedicle which connects the body with it is almost entirely composed of stroma-ingrowths, which form for the most part a very lax net- work of fibres and cells, though denser in the middle, and sur- rounding a slender cord of germinal cells, the sole remnant of the former epithelial pedicle. In a somewhat more advanced stage there is an identical structure with that just described as regards the specialization of the peri- pheral layers and the mass of central cells; the formation of yolk has, however, gone on much faster, and the follicular cells, as well as most of the cells of the central mass, are crammed with variously sized yolk-spherules. Here and there, especially in the periphery of the central cells, are irregularly shaped masses of yolk-spherules (fig. 24, a), among which are occasionally discernible nuclei like those of the surrounding cells. A comparison of Plate LIV. fig. 24 with Plate LITT. fig. 11 will show how very similar in size and extent these irregular patches of yolk are to the patches of amorphous deeply staining protoplasm in the earlier stage; and I cannot but think that they are these same patches of protoplasm produced by the fusion of some of the central cells which have commenced to form yolk-particles on their own account. Other preparations, again, seem to indicate that the fusion of certain of the central cells either does not take place at all, or takes place after the formation of the yolk. I have a nearly complete series of sections through an ovum in which the yolk has already commenced to be formed; the cells of the follicular epithelium are full of yolk-particles, as are also the central cells. The latter form a compact mass of cells containing abundant yolk-particles, but without any definite patches of yolk lying between the cells, such as could be compared to the patches of protoplasm formed by a fusion of cells. In many sections, however, of this series it happened that the central mass of cells had dropped out, so that I cannot make any positive statements about the point of discussion raised. This par- ticular instance showed very plainly indeed the connection of the mass of central cells with the follicular epithelium ; the area of con- nection was very limited, as has been already mentioned in other cases. The central cells are united with the follicular epithelium by a bridge of tissue which has every appearance of being an outgrowth of the latter; the nuclei are round and pressed close together as if in a condition of active multiplication ; they pass without avy break into the follicular epithelium, from the cells of which they cannot, indeed, be distinguished, and gradually on the other side into the mass of central cells. The cells of the latter have the ordinary characters that have been already described. I noticed a very large number of peculiar cells, several of which are illustrated in fig. 4 ; similar cells are not absent in other cases, but I never have seen them so numerous as in the present case. These cells are easily to be distinguished from the germinal cells among which they lie 34* 516 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [Dec. 7, by their smaller size, by their very deeply stained protoplasm, and by the fact that they nearly always contain a large number (3-5) of small nuclei close together. I have not yet succeeded in detecting these cells in the follicular layers, but I am nevertheless inclined to think that they are migratory leucocytes. I am at a loss, however, to account for the almost universal division of their nuclei into four or five. The presence of leucocytes in almost all the tissues and glands of the body is so well known that I need not give any detailed references ; the presence of these cells is not, however, to be con- founded with the migration of follicular cells. If, however, the identification of the follicular epithelium with a layer of immigrated leucocytes be right, there can be no distiuction between the two pro- cesses. The observations recorded in this paper, however, plainly show that in Protopterus at least there can be no possible confusion between follicular cells and lymphoid corpuscles, which is contra- dicted by so many other developmental facts. Unless it can be shown that lymphoid cells may arise from the direct metamorphosis of germinal epithelial cells it is quite absurd, in the present case at any rate, to allow any homology between follicular cells and im- migrated white lymph-corpuscles. Stege 111.—In this stage (figured diagrammatically in fig. 3, plate xxviii. of my former paper) the follicular epithelium is undivided from the ovum by any trace of membrane; the celis of which it is composed have dwindled down to a single layer ; their diameter bears a very small proportion to that of the enclosed mass of yolk, which has enormously increased in size. The cells of the follicular epithe- lium are still filled with yolk-spherules presenting no differences from the yolk-spherules which make up the substance of the con- tained mass. Their nuclei are conspicuous and round in shape. The follicular cells appear to continue to take a share in the nutrition of the body from the fact that they are large and well developed, and that the interstices of the protoplasmic network are largely filled with yolk-spherules: occasionally (e. y. figs. 7, 8, a) the nuclei of the folli- cular cells showed signs of degeneration ; this is probably preliminary to the evacuation of the cell-contents into the interior. Here and there the follicular cells appeared to be proliferating, the budded-off cells moving into the interior ; two such instances are shown in figs. 7, 8. It is of course a difficult matter to decide how far the appear- ances shown in the two figures cited are due to the proliferation and migration inwards of the follicular cells; they might be explained, by reference to earlier stages, as central cells which have still re- mained in contact with the follicular layer, only that they occur on all sides, and it has already (p. 511) been stated that the central cells are only in contact with the peripheral for a limited area. On the other hand, a careful comparison of the example from which fig. & is taken with another in pretty much the same stage of development, only younger, as evinced by its smaller size, reveals the important fact that the larger contains, in any given section, a larger number of cells in its interior than the smaller. The larger was rather more 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOL. 517 than twice the size of the smaller body selected for comparison ; the number of cells in the interior was in correspondence with their difference in size. ‘The larger had an average of 64 cells disseminated through the yolk in any given section, the smaller 42; hence the proportion between the two is as 3: 2. I am inclined to lay all the more stress on the mathematical statement of the case, as it allows extremely wide limits for possible errors of computation. On the hypothesis that none of the cells contained in the yolk during later stages are derived from the migration inwards of follicu- lar cells, it is obviously necessary to assume that they are all produced by the division of the central cells, or by certain of these cells which have persisted without division. It is true that the nuclei of the central cells in the earlier stages do multiply, but it is equally certain that others degenerate and disappear; and it seems to me that more undergo the latter than the former change; and I find that in the stage referred to above the smaller body contains considerably fewer cells in any given transverse section than in Stage I. It would then be expected that the larger bodies would contain fewer and fewer cells in their interior. I have, however, just stated that the result of my calculations’ in this respect has been in the direction of proving an increased number of cells in the more mature bodies. Now, assuming that I have made so large an error as 3 of the total number of cells in the larger, the two would still contain an equal number of cells disseminated through the yolk. But on the hypo- thesis there ought to be a very considerably less number of cells in the larger body. It is clear therefore that this hypothesis cannot be maintained ; and as there is no ground for assuming any third origin of the cells, it seems most probable that they have been largely derived from the proliferation of the follicular layer. Among those which I have included in this same stage are many that are probably, owing to their smaller size, younger than others which are larger. I have not, however, thought it worth while to separate these into two distinct stages, since they are both charac- terized by the extraordinary activity of the follicular epithelium, and by the presence of masses of yolk in the interior of the follicle, in which are imbedded namercus cells, themselves filled with yolk- spherules. As a general rule the smaller bodies belonging to this stage can be distinguished from the larger by the more crowded follicular celis; these are smaller, placed closer together, and not. confined to a single layer in the smaller, and therefore less mature, specimens ; in the larger bodies these cells have increased in size, the nuclei are not so crowded together, and the cells form but a single layer. This condition can hardly have been arrived at by the mere mevhanical growth in size of the whole body, which would tend to stretch, and therefore to reduce to a single layer of cells, the follicular epithelium ; the cells themselyes must either have dege-~ nerated, evacuating their contents into the interior, or must have 1 T have also calculated the number of cells contained in the interior of two other pairs of ova belonging to this stage, and of about the same relative size. 518 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [ Dec. 7° migrated into the interior ; the principal evidence is in favour of the latter supposition. The central mass itself is, as already stated, mainly occupied by a mass of yolk-spherules; these are deeply stained by the colouring- reagent. Among the mass of yolk-spherules are numerous cells which are more scattered in later stages; many of them are in course of degeneration, as evinced by the characters of the nuclei. In my former paper I have figured (/oc. cit. pl. xxix. figs. 9-20) a number of such cells, and need not refer to the matter again here. In no case could I observe the faintest trace of a germinal vesicle, nor does any one of the cells found in the interior of the body show any preponderance in size, or difference of any kind from the rest. The vascular layer is highly developed in this stage, in accord with the rapid growth of the follicular cells. Outside the vascular layer is the secondary follicle-layer, which has much dwindled in importance, and has a still closer resemblance to stroma than it had in the earlier stages. CONTENTS OF THE OvARy OF CERATODUS. The ovary of Ceratodus, like that of Protopterus, contaius, besides the ordinary ova which follow a normal course of develop- ment, other remarkable structures similar to those of Protopterus. The normal kind of ova, which are by far the most abundant, repre- sent a single cell, and agree in most details of structure with the ova of Amphibia and the corresponding ova in Protopterus. The mature ova are filled with rounded yolk-spherules approximately of equal size, and entirely unstained by prolonged immersion in borax carmine ; the periphery of the ovum is occupied by a delicate layer of egg-protoplasm in which pigment-granules are imbedded ; the egg is covered by only a single membrane, which is moderately thick with radial pores; the follicular epithelium is a single layer of flattened cells, of which the nuclei alone are obvious in my preparations. Some ova belonging to this stage are figured by Ayers in his paper. In rather younger ova there is a ball of protoplasm in the centre surrounding the germinal vesicle, and not yet invaded by the formation of yolk; the germinal vesicle has a peripheral row of germinal spots as in Protopterus. The formation of the yolk appears also to be on the whole very similar to the process described in Protopterus. Aggregations of yolk-granules make their appear- ance throughout the ovum, but do not seem to be confined at first to the peripheral layers. In the younger stages the yolk-particles are deeply stained by borax carmine, but not in the adult ova. I have already stated in the remarks introductory to this paper that, as regards my specimens, Ceratodus differs from Protopterus in the extreme rarity of those bodies which are apparently formed by a fusion of a number of distinct cells. So very rare are these structures that after a diligent search I only succeeded in discovering a single ease which could be in all probability referred to Stage I. in the developmental history of Protopterus (see p. 508). Certain other 1886.] | STRUCTURE OF THE OVUM IN THE DIPNOI. 519 problematical structures will be described in this portion of my paper, although they do not appear to belong to the same series as that which I shall now describe. The body (fig. 25) is decidedly smaller than in Protopterus; it corresponds, however, very nearly to the stage illustrated in fig. 9 of Plate LIII., and which is fully described on p. 513, where the slight differences which it presents from other individuals belonging to Stage I. are pointed out. The correspondence is in structure as well as in size. The body is placed at some little distance from the external surface of the ovary, but is connected with the germinal epithelium of the surface of the ovary by a slender pedicle of cells; it con- sists, like the corresponding structure of Protopterus, of a hollow sphere of cells which enclose a central mass ; the peripheral and central cells are also more or less independent. The peripheral layer of cells forms a continuous whole, but a closer examination shows it to be made up of two layers which are occasionally very distinctly separable from each other. The outermost layer appears to have originated from the germinal epithelium; its nuclei are large, rounded, or oval, and closely pressed together; the cells themselves, which contain these nuclei, have for the most part a stroma-like appearance (see p. 508). Within this layer, which is often several cells thick, is a layer of blood-vessels ensheathed in a mass of tissue of a fibrous retiform character, the fibres (fig. 25, a) for the most part forming a layer running parallel with the cireum- ference of the ovum, with interspersed nuclei; this tissue, from its general appearance and from its intimate connection with the blood- cavities (fig. 25, 41), is probably derived, like the blood-vessels, from ingrowths of stroma. The nuclei of this presumed stroma-layer are on the whole more elongated in form than those of the outer layer ; the blood-vessels were gorged with blood. The central mass of cells is probably during life in contact with the peripheral layers, but it appeared to be for the greater part at least quite distinct from it, there being no transition between its cells and those of the peripheral layers. The central cells appear to be closely similar in structure to the corresponding cells in Protopterus; the protoplasm of the cell is reticulate with large spaces left between the individual strands which form the network; the nucleus is of moderate size, round or oval in shape. Here and there (figs. 25, 26, f.e) some of the central cells were disposed in a row, one cell thick, round the periphery, closely applied to the innermost (stroma) layer of the peripheral layers. This is possibly to be compared to the true follicle-layer in Protopterus. Although, as I have already stated, the material at my disposal in the case of Ceratodus was not well preserved, certain portions of the ovary were in a better condition than others, and, generally speaking, it was quite possible to make out the relations of the different parts of the organ, both the stroma and contained ova, as well as occasionally the germinal epithelium on the outside; the minutiee of structure of the different cells were disguised by the inferior 520 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [Dec. 7, state of preservation, but in most cases the nuclei were very well preserved indeed, showing the rounded or oval form and the granular contents. This will not apply to the germinal vesicle of the ova, which were usually rather altered, showing, however, the peripheral layer of germinal spots. It does not seem likely, therefore, that the structure just described has been so altered as to render its identi- fication impossible. As already said, the evidence of the existence in Ceratodus of the structure formed by a fusion of cells depends upon only one case, which is an early stage corresponding to that of Protopterus figured on Plate LIII. fig. 9. This is the only example that I have succeeded in finding after a careful examination of many hundred sections. Besides these, my sections of the ovary contain a few peculiar structures, displayed in figs. 3, 21-23, which are cer- tainly not referable to the same series as the last, and concerning the nature and homologies of which I am in great doubt. The material at my disposal was not sufficiently well preserved to enable me to speak with certainty as to every detail of structure; and I only succeeded in finding a very few of the bodies in question, so that the following account is necessarily meagre. In fig. 3 of Plate LII. is represented what I believe to be the earliest stage: it consists of a spherical mass of cells bounded externally by an apparently structureless membrane, which separates them from the surrounding ovarian stroma (a); the cells are mainly disposed round the periphery of the sphere, the centre of which 1s largely oceupied by spaces in which there is no trace of any fluid ; the cells are small and rounded, with a large spherical or oval nucleus ; the nucleus, but not the cell-protoplasm, is deeply stained by the reagent used (borax carmine). The cells are exactly similar to the germinal cells so far as I could see; and the conditions I shall describe in the next stage lead me to infer that they are derived from the germinal epithelium. The second stage differs from that just described in being still continuous with the germinal epithelium; this fact would seem to point to its being an earlier stage than that just described, were it not for another difference in its structure. The body consists, like the last stage, of a mass of cells, but in the interior is a patch of gra- nular substance, which shows a different reaction to the staining- fluid. It is bardiy at all affected by the borax carmine and has a yellowish tinge. This central mass encloses here and there a few of the more peripherally-placed cells. Of the next two stages, displayed in figs. 21-23, I am uncertain which ought to be regarded as the earlier. In both the mass of ceils has dwindled down to a single layer of peripherally-placed cells (6), which, as before, are separated from the stroma of the ovary by a conspicuous and apparently structureless membrane. In the centre of the cells is a spherical or oval mass of a substance somewhat granular in appearance, which is not separated from the peripheral layer of cells by any membrane, but only by shrinkage. This mass (figs. 2] and 22) is of a yellowish tint, hardly 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOI. 524 affected by the borax carmine, and is throughout of a similar struc- ture; there is no structure resembling a nucleus to be seen. This central mass is clearly a further development of the condition described in the second stage. In one example, displayed in fig. 23, there is a difference from the condition just described in the presence of a few cells imbedded in the central mass, but clearly distinguishable from it by the nuclei being deeply stained. The cell-protoplasm was, however, hardly distinguishable from the surrounding mass. In the other example (fig. 21) the central mass contained no such cells. With the exception that it possesses no nucleus, this structure resembles very closely Platner’s figure of the Gasteropod ovum ', which contains a number of cells (‘‘ Nahrzellen’’) within its substance, derived from similar cells lying around the ovum. The first two stages described are about equal in size; the latter two are also about equal to each other, but considerably larger (twice the size) of the former. The comparison of sizes quite supports my identification of the latter two as the later stages in development ; and there can be no doubt, I think, that they all belong to the same series. These structures obviously bear a certain resemblance to the multi- cellular bodies in this fish and in Protopterus; and if I had not succeeded in finding in Ceratodus another structure undoubtedly corresponding to the multicellular body of Protopterus, I should have certainly regarded the structures at present under discussion as the representatives of the latter. The principal difference appears to be the non-formation of any secondary follicle-layer, the absence of any special vascular supply, and the fact that yolk is not formed in the early stages. With regard, however, to the apparent absence of the extra-follicular layer, it must be remembered that the close resemblance of the layer to a layer of stroma-cells has already been dwelt upon (p.508). It seems to me very possible that the structure just described is formed by the fusion of the protoplasm of the centrally-placed cells, the nuclei themselves gradually disappearing. An examination of better material must, however, settle the question. General Conclusions, und Comparison of Ova with those of other Vertebrates and Invertebrates. The general conclusions to be drawn from the facts, in so far as they refer to the Dipnoi, have been partly summed up in the résumé at the end of my former paper on this subject. It may be taken as a proved fact that the ovary in the Dipnoi contains two kinds of struetures developed from the germinal epithelium. The first kind is an ovum, the equivalent of a single cell, and is similar in all essentials to the cvum in the Amphibia. The second structure, which is very commonly met with in Protopterus and but rarely in 1 “Zur Bildung d. Geschlechtsproducten bei den Pulmonaten,” Arch. f. mikr, Anat. Bd. xxvi. (1886) p. 599. 522 MR. F. E. BEDDARD ON THE DEVELOPMENT AND [Deec. 7, Ceratodus, is the resultant of a large number of cells the protoplasm of some of which undergoes certain changes and forms a more or less fluid mass with the original nuclei suspended in it ; this mass appears around and between the rest of the cells, which are destined for its nutrition. The whole structure is surrounded by a definite follicular layer, which also shares in its nutrition by the formation of olk in its cells and their proliferation inwards. These bodies are surrounded by cellular layers which correspond exactly to the layers which surround the ova of other vertebrates; the difference is that instead of there being a single cell which grows at the expense of the rest, the interior of the mass is formed by numerous cells, all equi- valent. The bodies may be distinguished as multicellular or plasmodial from the ordinary unicellular ova. The share which the follicular epithelium takes in the nutrition of the ovum, I have discussed in detail in my former paper and need not refer to it again here, except to remark that the elaboration of food-material in the follicular layer and its absorption by the ovum has of course no relation whatever to my view that the ovum is a cell-complex. Certain writers have adduced arguments of this kind as a disproof of the unicellular nature of the ovum, which to my mind have no force. On the other hand, the developmental facts with respect to the cells within the follicle appear to me to be difficult to interpret otherwise than on the assumption that the ovum has the value of more than a single cell. It is true that I have been unable to detect any earlier stages than the one figured on Plate LII. fig. 1; but the intermediate stages between that and the mature ovum are fairly complete. The dis- covery of the earlier stages is of great importance; it would decide among others the very important question whether the central mass of cells is, or is not, derived from primitive ova recognizabie as such in the germinal epithelium, and whether or not the central mass of cells is formed by the migration inwards of a number of these cells or by the repeated division of one. But, whatever may be the answer to these questions, I have, I think, proved that the ovum is formed out of this central mass of cells. Some of these cells are apparently used as pabulum, but others fuse together into a mass of semifluid substance, which bears a very close resemblance to the liquor folliculi of the mammalian follicle. The resemblance is still more striking if we accept Waldeyer’s statements that the liquor folliculi is produced by a direct metamorphosis of the follicular cells, their nuclei remaining, as in the case of Protopterus, suspended in it. This substance, however, in Profopterus has not a mere passive function, serving, as in the mammal, to aid in the expulsion of the ripe ovum, possibly also in its nutrition ; it retains the activity of the cells from which it is derived and secretes yolk ; it must therefore be looked upon rather as a plasmodium of these cells than a product of their degeneration, although its deep staining with borax carmine, as opposed to the very light staining of the remaining cells, indicates some chemical change. Furthermore, there is no evidence of any 1886. ] STRUCTURE OF THE OVUM IN THE DIPNOI. 523 oue of the cells, which compose the central mass of the follicle, acquiring a predominance in size over its neighbours or being differ- entiated in any other way. The fact of there being two kinds of ova with a different mode of development is not new to the Vertebrata. In my former paper I have compared the follicle and its contents in Protopterus to the ‘*egg-nest” of Elasmobranchs, the points of difference being perhaps on the whole greater than the points of resemblance. But, since the formation of “ egg-nests” is so general among the Vertebrata, it seems to me that there is probably some genetic connection between these structures and the “egg-nest”’ of Protopterus. It has been shown that in Mammals, Elasmobranchs, and Reptiles the permanent ova are formed in two ways:—either (1) by the direct development of one of the primitive ova, which surrounds itself with a follicular layer derived from the ordinary undifferentiated germinal cells; (2) a number of primitive ova coalesce together to form anest ; their nuclei multiply, and some atrophy, serving as pabulum for a limited number which subsequently separate off, accompanied by some of the undifferentiated germinal cells, to form as many ova. These two modes of development are not regarded by Balfour as morphologically very different ; the latter mode of development has been brought about to secure the adequate nourishment of a certain number of cells which form the permanent ova. Balfour’s* observations certainly do not show any morphological difference between the ova produced in these two different ways; in both cases the ovum is the equivalent of a single cell; but the physiological difference is considerable. I have referred above (p. 512) to the presence of two kinds of cells among the central cells, distinguishable by the characters of their nuclei; in some the nucleus was rather larger and more oval in form than in others, where it was smaller and rounder, and, in fact, exactly like the nucleus of a follicular cell. It is possible that the cells with larger nuclei correspond to primitive ova and the smaller to the ordinary germinal cells ; in this case the resemblance of the central mass of cells to the egg-nest of the Elasmobranch will be dimin- ished ; against this supposition is the fact that there are nuclei of intermediate size, but these may have been produced by a recent division of some of the other nuclei. Judging from analogy, however, it is probable that some of the cells of the germinal epithelium are specialized into primitive ova from undifferentiated germinal cells, although in patches of germinal epi- thelium covering the ovary I failed to detect any such specialization in the nuclei. The important facts to be borne in mind in comparing the ege- nest of the Elasmobranchwith that of the Dipnoi® appear to me to be the early formation of the complicated follicular layers in the latter and the early commencement of yolk-secretion. The germinal cells being 1 Balfour, loc. cit. ? It is important to remember that the formation of ‘‘nests” is not confined in Elasmobranchs to the embryonic period (see Balfour, loc. cit, p. 415). . 524 MR. F. E, BEDDARD ON THE DEVELOPMENT AND [ Dec. 7, filled with yolk-particles at the expeuse of their protoplasm must tend to lose their activity for movement, their energy being spent in the elaboration of yolk; again, the thick layer of cells surrounding the central cells would prevent any of the central cells from leaving the interior of the follicle; the result of further growth would therefore necessarily lead either to the development of a number of distinct ova remaining permanently within the follicle, or to the excessive development of one of the cells, which would ultimately form the ovum, or, finally, to the formation of a single ovum out of the whole mass of cells. There are no facts which point to the truth of either of the first two alternatives, while all the facts at my disposal appear to prove the third alternative ; accordingly the temporary fusion of the primitive ova in the Elasmobranch nest and the degeneration of some of them becomes permanent in the Dipnoi, the ovum being the equivalent of a whole “nest.” Both Pale- ontology and Anatomy point to the great age of the Dipnoi, which may therefore easily be supposed to have retained ancient characters in the structure of the ova, as they undoubtedly have in the structure of the genital ducts. It is more generally believed that the Elasmo- branchs are ata still lower level of organization; if, however, as Mr. Howes has pointed out to me, the Chimeroids are the ancestors both of Elasmobranchs and Dipnoi, it may as easily be supposed that the egg-nest of the former has been derived from the egg-nest of the Dipnoi, as that the converse process has taken place. In this case the temporary fusion of primitive ova in the Sharks and Rays is a reminiscence of their permanent fusion in Protopterus and Ceratodus. It does not seem to me possible at present to say which of these views is correct; nor indeed can any comparison at all of the two structures have any great weight until the structure of the ovary has been thorovghly examined in such types as Chimera and some of the more primitive Sharks. On the whole it appears to me possible to regard these remarkable structures in the Dipnoi as corresponding to the egg-nests of other Vertebrates ; but the apparent absence of any protoplasm in the yolk-mass renders it extremely unlikely that the structure develops into an embryo’; on the other hand it is often very difficult, in an ovum full of yoik, to distinguish the protoplasmic matrix; it is probable, however, that these structures do not undergo any further 1 TI observed several ova undergoing degeneration—in one case belonging to the type discussed here. The follicular epithelium was in a condition of active degeneration, the cells becoming detached and passing into the inte- rior of the ovum. (This process is not to be confounded with the nutrition of the ovum by the follicular cells recorded in this paper and in my last; in the latter case the follicular cells are large, crammed with yolk-particles, and remain a continuous layer; in the degenerating ovum the follicular cells have decreased in size, contain little yolk, and great gaps are left by the disap- pearance of the cells.) The yolk has also undergone great changes, the yolk- spherules exhibit a vacuolated appearance and are of more irregular size, as if a number had become conyerted into fat-drops and had run together; the amount of yolk also was less, and the ovum in consequence was collapsed and of irregular shape ; at several points the walls of the ovum were altogether in- distinguishable. The way in which the oyum degenerates does not in fact 1886. | STRUCTURE OF THE OVUM IN THE DIPNOI. 525 changes, though the degeneration of a few out of an immense number (see footnote) is hardly proof of this. IfI were in a position to deny the presence of a germinal vesicle, the absence of this essential element in the ovum would be evidence of some force in the same direction. On the other hand, the energy showed by the central cells and the cells of the follicular epithelium would be entirely thrown away in this case ; and it is very difficult to imagine the continuance of such a wasteful process in the ovary—the organ chiefly concerned with the preservation of the race’. A formation of ova in the Vertebrata by a fusion of cells has been stated to exist, but has been subsequently denied. Goette’s observations on the formation of the ovum in Bomdi- nator”, referred to in my former paper, have been explained away by Nussbaum *, who considers that the polynuclear condition described by Goette is the result of the proliferation of the nucleus of a primitive germinal ceil, and is not produced by the approximation of the nuclei of a number of distinct cells which subsequently are fused. The observations of v. Siebold* are of interest in relation to this question. In Apus the ova are formed in spherical acini which containa number of cells of which one grows at the expense of the rest. This cell finally comes to occupy the whole of the interior of its acinus, the remaining cells dwindling indefinitely ; the nucleus disappears, and yolk-formation sets in. When the cell has been, for the most part, con- verted into yolk it moves down the duct which connects the acinus with one of the branching tubes of the ovary, and there fuses with one or more cells which have been produced in other acini by a similar course of development. The fused mass becomes surrounded by a membrane, and is the ovum. In my preliminary notice in the ‘ Zoologischer Anzeiger’ I have referred to the observations of v. Siebold, and differ very widely from a description (Arch. fiir mikr. Anat. 1886) of the degenerating ovum of the trout. I may also take this opportunity of referring to an ovum of Ceratodus in a similar condition of degeneration. I erroneously mentioned this ovum (Zool. Anzeig. No. 236) as a nearly fully mature ovum belonging to the multicellular or plasmodial type; it may very likely belong to this type, but the appear- ances which it presents are indicative of degeneration, and not of maturation. The follicular epithelium is not separated by any membrane from the contents cf the ovum (fig. 2); its cells in a few cases are loaded with brown pigment, and many of them haye migrated into the ovum, the contents of which have been largely absorbed, probably by these cells; in consequence of this the ovum is collapsed. I have noticed a similar state of affairsin the ovary of a newt (Molge waltiii), which I purpose to describe on some future occasion. 1 Tt has been suggested to me, in conversation, by Prof. Lankester that these structures may serve as food for the embryos, being deposited along with the ova, or that they may be reservoirs of nutritive material aiding in the growth of the intra-ovarian ova. Wither of these suggestions appears to me to be extremely plausible. ? Arch. f. mikr. Anat. Bd. xviii. * Entwickelungsgeschichte der Unke. * Beitrige zur Parthenogenese der Arthropoden. Leipsic, 1871. 526 MR. F. E, BEDDARD ON THE OVUMIN bienor. ([Deec. 7, erroneously stated that there had been no confirmation or refutation of the truth of his discoveries; I find, however, that I have un- wittingly ignored the contents of a paper by H. Ludwig’, in which there are described a series of important investigations of the ovary of Apus. Ludwig finds that there is nothing abnormal in the formation of the ova, and that a number of them do not coalesce as stated by v. Siebold; at least there is no real fusion of the ova, only an accidental running together of the contents of several acini due to ruptures. Ludwig’s account is so circumstantial, that there can be no reasonable doubt that the ova of Apus are not formed by the concrescence of several cells. The only other instance that I am acquainted with in which the ovum has been stated to arise from the fusion of a number of cells is in the Rotifer Lacinularia. A curiously similar mode of development of the ovum has been recorded by Huxley in Lacinularia. A number of cells of the ovary become compacted together, enclosed in a common mem- brane, and break away to form an ovum, which is, according to Huxley , never fertilized but develops parthenogenetically. It is true that the statement about the non-fertilization of these ova has been questioned by a later observer’, but much weight must obvi- ously be given to the observations of the discoverer of the formation of the ‘ winter ova’ in Lacinularia. The mode of origin of these ova is closely parallel to that which I have described above in Protopterus and Ceratodus. The ovary in the Rotifer consists of a mass of cells, some of which develop into ova, and all of which are comparable of course to the germinal cells in the ovary of the Vertebrate. The fusion of a number of these to form a single ovum is therefore clearly analogous to the fusion of a number of germinal cells in Protopterus and Ceratodus. EXPLANATION OF THE PLATES. Puate LIT. Fig. 1. Multicellular body in ovary of Protopterus, Stage I. g.e, germinal epithelium on surface of ovary; /-¢, follicular epithelium; fe’, se- condary follicle-layer ; 0/, blood-vessels ; c, central cells; », nuclei of central cells; p, mass formed by the fusion of the cell-protoplasm of central cells. . A portion of an adult ovum of Ceratodus in which the egg-membranes have disappeared prior to degeneration of ovum. a, stroma-layer ; Fé, follicular layer; y, yolk-spherules. . Nest of germinal cells in ovary of Ceratodus. a, nucleus of stronia- cell; 4, follicular layer; d, central cells. . Lymph-ceils (?) from multicellular body of Protopterus. . Nuclei of germinal cells from secondary follicle-layer of body, illus- trated in fig. 1. a, a nucleus from one of the same cells on the side of the body opposite to the area of invagination. Prats LITI. Fig. 6. Transverse section through a portion of outer surface of multicellular bo oOo, jet) ' Arbeit. a. d. Zool.-zoot. Inst. Wiirzburg, Bd. i. 2 See Cohn, Zeitschr. f. wiss. Zool. Bd, vii. (1856). P. Z.S. 1866: Pl. Ulla FEB. del: J. Smit ith. | STRUCTURE OF OVUM IN THE DIPNOI . P.Z.S. 1886. Pl. La fo) { OO.0.04 ogo? a az ee 0 0 £e a 6 alee y oe ng fa'@! Ge 444 Ps EO Cae 2 FEB. del, J. Smit th. Hanharb STRUCTURE OF OVUM IN THE DIPNOL. P78. 1886. PL-LIV. FEB del. J. Smit lith STRUCTURE OF OVUM IN THE DIPNOI. 1886. | ON SQUALORAJA POLYSPONDYLA. 527 body (Plate LIT. fig. 1) in a later stage. Lettering as in last plate. Fig. 7, 8. Orranees sections through a portion of outer surface of multicel- lular body in a later stage. a, degenerating nuclei ; other lettering as before. 9. Multicellular body from.ovum of Protopterus, differing from that illustrated in fig. 1 mainly by the absence of follicular layer. Lettering as before. 10. Portion of secondary follicular layer at point marked with an arrow in preceding figure; more highly magnified. 11. Central mass of a body belonging to same stage as that figured in fig. 9, to show the mass (p) formed by the breaking down of the central cells (c), the nuclei of which (7) are here and there imbedded in it. 12. One of central cells (Plate LII. fig. 1,c) with a large number of nuclei. 13. Three central cells from Stage I. (fig. 1, 4), to show difference in nuclei. 14-20. Central cells very much enlarged from Plate LIT. fig. 1, to show the different stages in degeneration of nuclei. 21. Nest of germinal cells in ovary of Ceratodus at a later stage than that in Plate LII. fig. 3. Lettering as in that figure. Puate LIV. Fig. 22. A portion of body represented in Plate LIIT. fig. 21, more highly magnified. Lettering as in fig. 21. 23. Nest of germinal cells in ovary of Ceratodus at a stage near to that represented in figs. 21 and 22. Lettering as in those figures. 24, Portion of multicellular body in ovary of Protopterus, to show masses of yolk (a), apparently corresponding to areas occupied by fused masses of protoplasm in earlier stages (p in figs. 1, 9, and 11). 25. Multicellular body of Ceratodus at a stage corresponding to that of Protopterus, illustrated in fig. 1. a, fibrous tissue of stroma-layer ; other lettering as in fig. 1. 26. A portion of central cells of multicellular body of Ceratodus, more highly magnified. Lettering as in fig. 1. 27-31. Central cells of multicellular body of Protopterus at an early stage, to show commencing yolk. 32, 33. Central cells of ditto, to show disintegrating nucleus, 2. On the Anatomy and Systematic Position of the Liassic Selachian, Sqgualoraja polyspondyla, Agassiz. By A. Smith Woopwarp, F.G.S., of the British Museum (Natural History). [Received October 18, 1886.] (Plate LV.) ’SuMMARY OF Previous RESEARCHES. The prolific fish-beds of the Liassic formation have yielded so much valuable material during recent years, that it is now possible to considerably supplement the original anatomical memoirs of Agassiz, Egerton, and the other pioneers in early Mesozoic ichthy- ology. Many specific types that were at first only known from very 528 MR. A. S. WOODWARD ON [ Dec. 7, imperfect fragments are already represented by remains as complete as can be expected in a fossil state; and such remains being now forthcoming in the case of the remarkable Selachian, Squaloraja polyspondyla, it is proposed once more to bring this interesting form before the notice of zoologists. The first scientific account of the genus and species under consi- deration was communicated by Dr. H. Riley to the Geological Society in 1833, and subsequently published, with one slight modi- fication, in that Society’s ‘Transactions’*. A fine specimen in the Bristol Museum, displaying the head and vertebral column, with obscure fragments of the appendicular skeleton, formed the subject of this memoir, and notwithstanding the author’s limited means of comparison, he rightly recognized its affinities both with the true Sharks and the Rays, and expressed the circumstance in its generic name. Riley, however, misinterpreted the snout and rostral spine, regarding these as jaws, and originally suggesting the specific name of dolichognatha in allusion to their elongated shape; but Agassiz pointed out to him the error in time for correction in an appended note (J, c. p. 85), and the distinguished author of the ‘ Poissons Fossiles’ again figured and described the specimen in one of the later parts of his third volume*. Agassiz, indeed, was already acquainted with portions of the vertebral column and dermal tubercles of the fish, and had enumerated these in his preliminary manuscript notes under the name of Spinacorhinus polyspondylus ; but Riley’s prior description necessitated the adoption of the generic title Squaloraja, though his withdrawal of ‘ dolichognatha’ allowed the Agassizian specific name to be retained. But although Agassiz’s extensive acquaintance with the Selachian order enabled him to throw further light upon the Liassic genus, and point out its remarkable resemblances to the Pristiophoridze, he still failed to comprehend the precise nature of the curious snout, and it was left to Mr. William Davies, of the British Museum, with still more materials at his disposal, to offer a complete explanation. Tn an important paper in the ‘Geclogical Magazine’ for April 1872°, he pointed out that the uppermost rostral prolongation was a true spine, homologous with the frontal spine of the male Chimeroid Ischyodus orthorhinus, then made known by Sir Philip Egerton ; and he further demonstrated the absence of the appendage in some individuals, which were naturally regarded as females. Davies, moreover, added some notes on the vertebral column, and Hasse has more recently * published an account of the structure of the vertebrae ‘in great detail. 1H. Riley, “On the Saualoraja,” Trans. Geol. Soc. [2] vol. v. 1833, pp. 83- 88, pl. iv. 2 L. Agassiz, ‘Recherches sur les Poissons Fossiles, vol. iii. p, 379, pls. 42, 43. 3 W. Davies, ‘On the Rostral Prolongations of Sgualoraja polyspondyla, Ag.,” Geol. Mag. vol. ix. (1872) pp. 145-150, pl. iv. 4 0. Hasse, “ Einige seltene palaontologische Funde,” Palwontographiea, yol. xxxi. (1885) p. 4, pl. i. figs. 2, 3. 1886. ] SQUALORAJA POLYSPONDYLA. 529 New SPECIMENS. Up to the present time, therefore, there is no very precise infor- mation in regard to the structural features of Squaloraja beyond the descriptions of dermal appendages, the snout, and the vertebral column. But the British Museum again furnishes materials for an addition to our knowledge (thanks, especially, to a recent purchase from Mrs. Dollin of Lyme Regis, and the acquisition of the Egerton and Enniskillen collections), and it is upon the national fossils that the present contribution is based. All the specimens are from the well-known Lower Lias of Lyme Regis, Dorsetshire ; and, adding Roman numerals for convenience of future reference, they may be briefly enumerated as follows :— I. The nearly complete skeleton of a male, wanting only a small portion of the caudal region, and shown of the natural size in Plate LV. fig. 1. This specimen exhibits the dorsal aspect, and is parti- cularly interesting on account of the preservation of the limbs and limb-girdles, which have not hitherto been so well displayed. The cranial cartilages are not remarkably distinct, and the dentition is only feebly indicated ; but the form and proportions of the snout and rostral spine are very satisfactorily shown, and the vertebral column, except anteriorly, is in a comparatively good state of preservation. (Brit. Mus. no. p 2276.) II. Portions of the vertebral column and the crushed cranium of an old individual, probably female. (Egerton Collection, Brit. Mus. no. P 2079.) III. Portion of the skeleton of a young female, viewed from the ventral aspect. There are only obscure remains of the cranial cartilages, but the snout and dentition are beautifully exhibited. The caudal region is also well preserved, but all traces of the abdomen have been removed and destroyed. (Enniskillen Collection, Brit. Mus. no. p 3184.) IV. A fine skull of a male individual, seen from above, and exhibiting the form of the head, dentition, and rostral spine. (Brit. Mus. no. 47402.) V. A detached rostral spine, somewhat smaller and less robust than that figured by Davies (/. c. fig. 3), but equally curved, the broadened base of insertion wanting. (Enniskillen Collection, Brit, Mus. no. p 3186.) VI. A complete, much-curved rostral spine, exhibiting only the superior aspect. (Enniskillen Collection, Brit. Mus. no. p 3187.) VII. The anterior two thirds of a rostral spine, probably belong- ing to an animal even larger than no. II. (Enniskillen Collection, Brit. Mus. no. p 4574.) VIII. An extraordinarily slender and acuminate small rostral spine, seen from the dorsal aspect. (Egerton Collection, Brit. Mus. no. Pp 2081.) The specimens numbered I. to IV. are almost certainly referable to the already named species, S. polyspondyla, Ag., and owe their slight variability to differences in age, as indicated by the condition Proc. Zoor. Soc.— 1886, No. XXXV. 35 530 MR. A. 8. WOODWARD ON [Dec. 7, of the vertebral column. But the detached spines would appear to afford evidence of two or more forms as yet unrecognized, and the small example, no. VIII., is particularly distinct. It is very possible, indeed, that when more specimens of the genus are available for study, the characters of the rostral appendage will enter promi- nently into the diagnosis of each species; but I only venture, on present evidence, to distinguish the possessor of the small spine no. VIII. (Plate LV. fig. 6), and this may be appropriately designated by the name of S. ¢enuispina. The fossil in question is separated from its homologue in the known species by its much more slender and acuminate shape, and possibly, though not certainly, by the slight concavity of the proximal half of its upper surface. During the investigation of these fossils I have had the privilege of discussing the subject with several zoological and paleontological friends, to whom I am indebted for some valuable suggestions noted in the following pages. I desire especially to return thanks to Prof. W. K. Parker, F.R.S., for much kind assistance in regard to the skull; to Mr. G. B. Howes, for a continuance of the help so freely given on previous occasions ; to Mr. G. A. Boulenger, for the facili- ties afforded in the study of the recent Seiachians under his care ; and to my senior colleague, Mr. William Davies, to whose earlier work reference is so frequently made in the sequel. ANATOMICAL DESCRIPTION. External Form.—Commencing the description with a brief notice of the general external form of Sgualoraja, attention may be first directed to the beautiful specimen no. I., represented in Plate LV. fig. 1. As the shape of the head had already led Agassiz and Davies to suspect, the proportions are found to be very similar to those of the living Pristiophorus. Assuming that about three centimetres are missing from the tail of the specimen, the snout will have occupied one quarter of the entire length of the animal. The body must have been but slightly compressed from above downwards, and the pectoral fins were undoubtedly free, having no connection with the head; the shoulder-girdle, however, is placed relatively nearer to the chondrocranium than is the case either in Pristiophorus or Pristis, though appearances are not improbably deceptive, owing to crushing during fossilization. It is impossible, of course, to deter- mine whether the gill-openings were ventral or lateral, and scarcely any traces of the branchial arches have been preserved. The pectoral fins, as usual, are much larger than the ventrals, and the tail is long and slender, without spine, as admirably shown in no. ILI. (fig. 7). Unfortunately, all sure indications of dorsal and caudal fins are wanting, thongh it is scarcely likely that these appendages were absent in the living fish. Dermal Structures*.—In regard to the integument and its appen- dages, the new fossils afford some interesting additional information. No less than eight rostral spines are now available for study ; and ? The dentition will be more conyeniently treated in a later section, p. 534, 1886.] SQUALORAJA POLYSPONDYLA. 531 the specimens numbered I. and III. reveal a few hitherto unnoted facts concerning the arrangement of the small prickly tubercles. As already indicated in Davies’s large figure, but still more satis- factorily shown in our Plate LV. fig. 1, a series of the tubercles with especially long recurved hooklets is arranged along either edge of the prenasal (intertrabecular) cartilage ; and these two rows are precisely parallelled in the snout of certain living species of Rhino- batus (e.g. R. granulatus). But immediately at the base of the rostrum, where the cartilage is particularly firm and expanded into two lateral elevations (Davies, fig. 2), the tubercles become densely clustered in a manner not observable in the existing form ; and this arrangement is in intimate relation with the overlying spine. The disposition of the tubercles along the trunk, evenif originally regular, is now no longer evident, and none but scattered examples are to be seen ; but the slender tail was provided on each side with a longi- tudinal row of comparatively large recurved hooklets, upon inconspi- cuous bases, as is very well shownin the female, no. III. (fig. 7). A small tuft of these dermal structures also occurs at the extremity of each clasper in no. I. (fig. 1, 24), aud there are distinct indications of a patch of very minute prickles upon the membranous portion of the (right) ventral fin in the same specimen. In regard to the rostral spine, Davies’s figures and descriptions leave little to be added. The conclusion as to its absence in certain individuals (females) is confirmed in an interesting manner by the fossil no. I1I., which has been so ‘‘ developed’’ on the dorsal aspect that there cannot remain the slightest doubt upon the subject. But a new specimen, from the Enniskillen Collection (no. V. fig. 5), still further demonstrates its prehensile character in the individuals that possess it ; for a number of blunt conical tubercles, without radiated bases, are clustered together upon its inferior aspect (A) to oppose the group of more slender hooklets already described at the base of the snout. When well preserved (as in no. I.), the surface of the spine exhibits the reticulate impressions of the vessels in a once enveloping integument *; and on each side there is a marked longi- tudinal groove (fig. 5, g), which gradually disappears on approaching the distal extremity. The peculiar form of the spine is also worthy of note, more parti- cularly as it is repeated in two other cartilaginous fishes whose remains have been found in the same geological formation ; it differs but little from that of the rostral appendage in the chimeroid Ischyodus*, and is still more similar to another Liassic spine which there is some reason for suspecting may belong to the remarkable Prognathodus*. ‘The peculiar shape, indeed, taken together with 1 Mr. Boulenger has kindly helped me to determine that the corresponding appendage in the living Chimera monstrosa is likewise covered with skin. * Sir P. Egerton, “ On a new Chimzroid Fish from the Lias of Lyme Regis (Ischyodus orthorhinus, 3 ),’ Quart. Journ. Geol, Soe. vol. xxvii. 1871, pp. 275- 278, pl. xiii. 3 Sir P. Egerton, “ Prognathodus Giintheri (Egerton), a new Genus of Fossil Fish from the Lias of Lyme Regis,” Quart. Journ. Geol. Soc. vol. xxviii. 1872, pp. 233-237. 35* 532 MR. A S. WOODWARD ON [Dec. 7, the fact of its occurrence in more than a single type, leads to an interesting speculation, suggested to me by Professor Parker. Com- pared with the distinct anterior intertrabecular cartilage, which forms the axis of the rostrum in such primitive fishes as the glutinous Hags (Myzine)*, scarcely the slightest difference in form can be noted; and it seems not unlikely that we are here concerned with an admirable illustration of the principle, that the contours of super- ficial structures appended to the cranium are frequently determined, in the main, by the shape of the fundamental cartilages to which they are attached. The fossils, of course, do not permit a determi- nation of the complete form of the intertrabecular cartilage in any of these types, or of its primitive distinctness ; but the slight glimpses that can be obtained are rather favourable than otherwise to such a conclusion. Of the skin itself in Sgualoraja, only indefinite patches remain, and no small shagreen granules appear to have been developed in it ; but the sharp lateral edge, both of the rostral and caudal regions, is strengthened by a series ‘of minute calcified rings (fig. 1, d), evidently quite similar to those stiffening the boundaries of the snout in the living Pristiophoride. Cranium and Mandibular and Hyoid Arches.—Nearly all the large fossils under consideration reveal facts of more or less interest in regard to the structure of the skull; nos. I., 11., and IV., with Riley and Davies’s specimens, present the dorsal aspect, while no. III. and the fragment shown in Davies’s plate, fig. 4, afford some parti- eulars as to the conformation of the ventral surface. The palato-trabecular region (figs. 1, 2, pa.tr) extends far forwards in its present crushed condition, and from the centre is produced the long narrow intertrabecular cartilage (i.¢7) forming the axis of the snout. From each anterior outer angle of this region there also arises a more slender forwardly directed cartilage (pr. pa), which gradually tapers to an incurved point, as admirably shown in the left side of no. LV. (fig. 2). This prolongation evidently served to stiffen the edge of the base of the snout, exactly as its well-deve- loped homologue in the living Pristiophorus; and there can be little doubt that it:represents a definite prepalatine element, such as has not hitherto been recognized in the skulls of the Selachian order. Its form is almost identical with that of the corresponding cartilage in the Myxinoids, as will be at once seen on referring to Prof. Parker’s beautiful figures of Mywine and Bdellostoma®; in these fishes, indeed, the process serves a similar purpose, being like- wise placed to strengthen the sides of the rostrum. Immediately behind the origin of the prepalatine “ horns,” the lateral boundary of the palato-trabecular region gradually curves inwards for some distance, and then as slowly outwards again until it forms a well-marked antorbital prominence ; but the olfactory capsules, in their fossilized state, are totally unrecognizable, though 1 W. K. Parker, ‘‘On the Skeleton of the Marsipobranch Fishes.—Part I. The Myxinoids,” Phil. Trans. 1883, pl. x. fig. 2. 2 W. K. Parker, loc. cit, pl. x, figs. 1-3 and pl. xvii. figs. 1-3. 1886.] SQUALORAJA POLYSPONDYLA. 533 the two excavations at the base of the rostrum in the fragment shown in Davies’s fig. 4 evidently testify to their normal proportions and situation. Ina line with the prominence is fixed the base of the rostral spine (7.s), quite at the hinder extremity of the ethmoi- dal tract ; and still more posteriorly, the chondrocranium begins to exhibit considerable lateral compression, though finally widening to a slightly broader occiput. Extending backwards from the antorbital process, the slender postpalatine cartilage (pé.pa) is preserved in most specimens (especially in no. IV. fig. 2), but there is some uncertainty as to whether it formed a distinct element. It tapers slightly to its distal end, and the crushing during fossilization has usually imparted to it the deceptive appearance of connection with the hyomandibular. No postorbital process can be observed, and the circumstances of preservation are probably accountable for the absence of any trace of a fontanelle in the cranial reof; but there is an interesting V-shaped protuberance (a.v) close to the hinder extremity, evi- dently representing a fold round the hollow into which opened the aqueductus vestibuli (or ductus endolymphaticus) of each auditory sac. On the ventral aspect, the parachordal, or “ investing mass” (fig. 3, iv.m), is produced posteriorly into a pair of occipital condyles (oc.c), as already noted by Riley; and there is a well- marked median ridge (x), obviously due to the remains of the primitive notochordal sheath. A median foramen (c.f) is also some- what conspicuous, and, if not the result of accident during fossiliza- tion, is evidently the passage for the united internal carotid arteries proceeding to the pituitary body’. Of the mandibular and hyoid arches, the hyomandibular cartilage (figs. 1, 2, hm) is the only portion satisfactorily preserved. In its crushed condition it is seen to extend from each side of the occiput, curving outwards and forwards, and gradually tapering to the distal extremity. In shape it approximates to that of most “ Batoidei,”’ being twice as broad proximaily as distally, and its apparent eonti- nuity with the cranial roof is probably due to the process of fossili- zation. Not a trace of the pterygo-quadrate and mandibular cartilages appears exposed to view; but the arrangement of the dental plates in the specimen no. III. (fig. 3, ¢) shows that the two rami of the jaw met at the symphysis in a comparatively acute angle, and were not placed in the same straight line, as is the case in so many living Rays. But the most remarkable feature to be noticed in the skull of Squalorga is preseuted in the two pairs of transversely elongated appendages, with reflected ends, arising from beneath the narrow part of the palato-trabecular region. These curions structures are not well shown in our fig. 1 (cé.a, ci.6), but can be studied in their entirety in the large specimens figured by Riley and Davies. The most anterior (ci.a) is the larger, and is completely displayed on both sides of the last-named fossil ; its total length is equal to three times the width of the skull at the position where it emerges, * See T. J. Parker, ‘ Zootomy,’ 1884, p. 62, fig. 20. 534 MR. A. 8. WOODWARD ON [ Dec. 7, and for two thirds of its extent it is directed outwards and ex- hibits only very slight tapering; the distal third rapidly diminishes to a pointed extremity and is fixed at right angles to the rest in a backward direction. The hinder appendage (ci.4) measures only two thirds the length of the first, and is about half as broad; it likewise has an outward and posterior trend, but (in its fossilized state) is much more gradually arched. The relatively great size of these appendages renders them some- what difficult of interpretation, and it is scarcely possible to decide whether they consist of true cartilage or are merely dermal in cha- racter. In position they correspond very closely with the hinder labials of many living Selachians, and also with the supposed homo- logous rods that form the axes of the oral barbels in Myxinoids’. But in the latter group these appended “ feelers”? never seem to extend outwards to a length much exceeding half the breadth of the head; and the largest cirri with which I am acquainted in the Sel- achians are scarcely longer than the rami of the jaws. It seems likely, however, that the structures in Sgwaloraja are the gigantic representatives of the latter, which are elongated outgrowths of the cartilages of the nasal valves*. There is no evidence of anterior labials in the specimens of Squa- loraja already known. Dentition.—The dentition of Sgualoraja is very remarkable and has not hitherto been correctly noted. Some indications are to be observed in specimens I. and II., but the teeth are beautifully dis- played both in III. and IV.; moreover, the parts in these two instances are practically identical, showing that there were no vari- ations according to sex, as is the case among certain living Selachians (e.g. Raja). The dentition of both jaws is preserved in no. III. (figs. 3, 4), but only that of the right side of the mandible affords a good view of the grinding-surface. Each ramus bears only a single dental plate, sharply marked off in front from its fellow of the oppo- site side, and exhibiting towards the symphysis a gently tumid prominence. For the anterior two thirds of its length the plate is of nearly uniform breadth, but in the last third the outer border gradually trends inwards, producing a more or less pointed posterior extremity. And the efficiency of the grinding-surface is increased by a series of parallel longitudinal ridges or folds of the enamel, which are distinctly worn down towards the outer functional border. Eleven of these rugee can be counted on no. III. (fig. 4), while fourteen or fifteen are visible in no. IV ; but, except on the wrder surface of the plate in no. II., there are no traces of any sutures between them, and even in this specimen the evidence is somewhat obscure. It appears, however, that there were feebly marked longitudinal divi- sions corresponding to the several rugee, and that these became accentuated at the outer edge, allowing of the shedding of the worn- out portions as growth proceeded. 1 W. K. Parker, loc. cit. pp. 385, 399, pls. x., xvii. figs, 1-3. 2 The “ Nasenfliigelknorpel” of Miller; see O.Gegenbaur, ‘Das Kopfskelet der Selachier,’ pp. 97-111, pls. xvi., xvii. 1886. ] SQUALORAJA POLYSPONDYLA. 535 Vertebral Column.—In the subject of fig. 1 the vertebral column is beautifully shown beyond the shoulder-girdle, though somewhat imperfect in front. As already described by previous writers, the vertebree (fig. 8) are merely slender, concentrically marked rings, of the truly “‘ tectospondylic ’’* type, and in the space just mentioned no less than 340 can be counted; in the abdominal region, sixteen of these occupy the length of a centimetre, while in the tail the proportions are so slightly different that only one more ring is com- prised within the same distance. The obscure portion in front of the pectoral girdle measures one and a half centimetres in length, probably representing about 24 vertebre ; and if three centimetres are missing from the end of the tail*, this loss will indicate an additional 48. The total number is thus found to be approximately 400, as estimated by Davies in the large specimen described in 1872. In the more aged individuals (e. g., no. [I.) the vertebral rings are more robust than those of the apparently yonng (e. g., no. III.) ; and it is remarkable that in no example is there any trace of the fusion of the elements in the region of the neck. But it is not necessary to add a detailed account of the structure of the vertebra themselves, for they have already been carefully examined and described by no less an authority than Professor Carl Hasse, of Breslau®. As the result of his researches in this direction, the latter anatomist concludes that in Squaloraja ‘‘ we have to do with an ancestral form of the now living Pristidee, a form which, in its development, appears to have advanced beyond the existing Pris- tiophoridze, and also beyond the oldest Rhinobatidz,”’ which be has deseribed from the upper Oolite of Bavaria. The vertebral arches were not of sufficient consistency to leave the slightest trace in the fossil state. Appendicular Skeleton.—In the subject of fig. 1, as already remarked, the pectoral fins are sufficiently well preserved to exhibit their complete severance from the cephalic region and their corre- spondence in general character to those of the living Pristiophorus. But the remains of the supporting girdle are much less perfect and satisfactory, and the other known specimens do not appear to throw any further light upon the subject. There can be little doubt, how- ever, that the “‘ girdle’ was complete, as in the Rays proper, and the well-defined cartilage (s.sc) on the right is evidently the character- istic suprascapula. A faint trace of the posterior boundary of the transverse coracoid bar (cor) is also shown on the same side. The proximal cartilages of the fin are only two in number, and well preserved on both sides of the fossil, though most completely displayed on the left. The preaxial element (pms) is elongated in a transverse direction, and appears of almost uniform breadth, though its exact shape is evidently destroyed by crushing ; it is relatively small, having only about one quarter the size of the postaxial ele- 1 ©. Hasse, ‘Das natiirliche System der Elasmobranchier,’ allgemeiner Theil (1879), p. 44. ? The caudal region of the fossil is not completely shown in fig. |. °C. Hasse, “ Hinige seltene palaontologische Funde,” Paleontographica, vol. xxxi. (1885) p. 4, pl. i. figs. 2, 3. 536 MR. A. S. WOODWARD ON [ Dec. 7, ment. The latter (mtp) is triangular in form, and elongated antero- posteriorly ; the foremost border abuts against the hinder edge of the preaxial cartilage, which it equals in transverse extent ; and the inner border curves gradually outwards and backwards to meet the nearly straight external boundary ata posterior apex. Judging from the analogy of living Selachians with fins of a similar type, the posterior of these cartilages may be regarded as the metapterygium ; while the anterior element may represent the coalesced pro- and mesopterygium (as in Pristiophorus'), or it may be wholly meso- pterygial, with a minute, indistinguishable propterygium at its proximal angle (as in Heptanchus and Hexanchus*). Beyond the basal cartilages are arranged the cartilaginous rays of of the fin (7). These are somewhat obscured both in front and behind by remains of the integument, and it is uncertain whether the first attached to the preaxial element is stouter than the remainder; twenty rays, however, can still be counted on the right side, and there are traces of sixteen on the left; the foremost thirteen are directed almost transversely or outwards, while the following have a more marked backward inclination. The pelvic girdle and its appendages are rather more satisfactorily displayed than the pectoral structures just described. Anteriorly, on each side, the cartilage is prolonged into a remarkably strong prepubic process (p.pb), the base of which occupies one fourth of the entire breadth of the girdle; but the forward extent of the prominence is not determinable, owing to imperfect preservation. Posteriorly, on each side, is a long slender iliac process (2), especially well seen on the left, and slightly directed outwards ; itis much less robust than the prepubic, and appears of almost uniform breadth throughout ; in length it equals twice the width of the transverse pubic cartilage (pub). Arising immediately within the point of union of the pubic and iliac regions is the basal cartilage (5.8) of the pelvic fin, which exhibits no sutural divisions, and (this specimen being a male) is prolonged backwards into a powerful clasper (cl). It curves gradually inwards throughout the whole of its rayed portion, and is of almost uniform breadth. On passing into the claspers, the cartilage becomes more calcified, and perhaps slightly broader. The inner edge is straight, but the outer edge exhibits a gentle sigmoid curve, which results in the widening of the rounded terminal extremity ; and at the end of each clasper (especially the left) a smal] tuft of dermal hooklets (A/) is preserved. The fin-rays (7), which appear to be completely shown on the right, are altogether twelve in number, and the length of the supporting cartilage is scarcely more than one half of that of the appended clasper. There is no distinct evidence of one or more preaxial rays attached to the girdle itself, and the foremost exhibited is no longer than the remainder. 1 St. G. Mivart, “ Fins of Elasmobranchs,” Trans. Zool Soc. yol. x. p. 403, pl. Ixxviii. fig.1. * C. Gegenbaur, “Schultergiirtel der Wirbelthiere, und Brustflosse der Fische,” Untersuch. yergl. Anat. Wirb. 18665, pl. ix, figs. 1, 2. . 1886. } SQUALORAJA POLYSPONDYLA. 637 AFFINITIES AND Sysrematic Position. Proceeding, lastly, to a consideration of the systematic position of Squaloraja, it will be observed that the new fossils here described enable us to arrive at a much more definite conclusion than it has hitherto been possible to formulate. Agassiz has pointed out the affinities of the genus with the Pristiophoridw; Davies has further indicated some resemblances to the Rhinobatide, and been led, by his discovery of the rostral spine, to speculate at least as to its family distinctness ; while Ginther! has likewise refrained from more than a suggestion that it is nearly allied to the first-named group. That the animal is a true Selachian, there cannot be the slightest doubt ; nor does it require more than a superficial glance to recognize its resemblance both to the Sharks proper and the Rays. But (as already mentioned by Davies) the possession of a prehensile rostral spine by the male distinguishes Sgualoraja from all known members of the order, recent or fossil, and suggests affinities with the Chi- meeroids* ; while the enormous size of the barbels or cirri seems to have no parallel, at least among living forms. The dentition, too, is evidently unique, so far as our present knowledge extends, and the marked character of the symphysis is a feature of peculiar interest. Comparing the genus in other points with the various recognized families upon the “‘ borderland ” of the two sections of the Selachii, reference may first be made to the Rhinide. Though agreeing with this group in the very slight depression of the body, it is readily distinguished by the elongation of the snout and the inferior position of the mouth; and the anterior border of the pectoral fin is much less produced forwards, owing to the relatively smaller size of the propterygium. To the oft-mentioned Pristiophoride, Squaloraja bears a remark- able resemblance, both in the structure of the snout and the general form of the body; but there are no traces of teeth on either boundary of the rostrum ; and if the peculiar dental armature of the jaw may be quoted asa family character, this, too, will exclude the genus from the present group. From the family of Pristide, the Liassic form is still further separated by the characters of the head and its anterior prolongation, though agreeing tolerably well in the shape of the trunk and fins. There are also certain features that prevent its reference to the Rhinobatide. The structure of the pectoral fin in this family is quite distinct from that of the fossil, the propterygial element being pro- longed far towards the head, so that in some cases it is connected by skin with the cephalic region. Its distinctness from other families is too obvious to require any special mention, and Sgualoraja is thus excluded from all recognized divisions of the order. It may even represent a hitherto unknown ' A. Giinther, ‘Study of Fishes’ (1880), p. 835. 2 We regard the Chimeroidei as a distinct order, follow ing Professor Huxley, Proe. Zool. Soc. 1876, p. 57. 538 MR. P. L. SCLATER ON A NEW PARROT. [ Dec. 7, suborder, but I venture at least to suggest that the genus may be regarded as the type of a new family ; and utilizing, as far as possible, the structural features that commonly enter into the diagnoses of zoologists who study living forms, it may be provisionally defined as follows. Order SELACHII. Suborder TEcrosPoNnDYLI. Family SQuALORAIID. Body scarcely depressed, elongate. Head produced into along flat rostrum, without lateral teeth. Males with a prehensile spine on the upper part of the snout. Dentition sharply divided at the symphysis. Pectoral fins with smail propterygium, free. EXPLANATION OF PLATE LY. Fig. 1. Skeleton of Squaloraja polyspondyla (male), dorsal aspect. [No. I.] a.v, situation of auditory openings ; 6.5, basipterygium of pelvic fin ; ci (a and b), cirri; cl, clasper ; cor, coracoid; d, edge of skin ; h&, dermal hooklets; Am, hyomandibular; 2/, iliac process; itr, inter- trabecular rostrum; mfp, metapterygium ; oc.c, occipital condyle ; p-pb, prepubic process ; pa.tr, palato-trabecular region ; pms, preaxial basal cartilage of pectoral fin; p7.pa, prepalatine process; pt.pa, postpalatine (antorbital) process; pub, pubic cartilage; 7, cartila- ginous fin-rays; 7.s, rostral spine ; s.sc, suprascapula; 7, dentition ; v, vertebral column. 2. Skull of ditto (male), dorsal aspect. [No.IV.] Refs. as above. 8, Skull of ditto (young female), ventral aspect. [No. III] c¢.f, carotid foramen (?); zv.m, investing mass ; ”, notochordal sheath. 4, Dental plate of right mandibular ramus of ditto, twice nat. size. [\No. 1IT.] 5. Rostral spine of Sgualoraja, sp., side view. [No. V.] 4, hooklets; g, lateral groove. : 6. Rostral spine of Squaloraja tenuispina, dorsal view. [No. VIII.] 7. Tail of Sgualoraja polyspondyla (young female). [No. Hl] 8. Section of vertebra of ditto. [No. I1.] All the specimens are from the Lower Lias of Lyme Regis, and preserved in the British Museum. With the exception of fig. 4, the drawings are of the natural size. 3. On an apparently new Parrot of the Genus Conurus living in the Society’s Gardens. By P. L. Scuatmr, M.A., Ph.D., F.R.S., Secretary to the Society. [Received October 29, 1886.] (Plate LVI.) On the 29th of April last we purchased of Mr. Cross, of Liverpool, an example of a Parrot of the genus Conwrus, which seems to be different from every other species of the genus yet described. The bird, which is still living in the Parrot-house, is at once distinguish- able from its congeners by its red throat and collar, whence I propose to call it pupa : J. Smit del et lith. : : P7Z.5. 1666. PI aR IeGL Fa es ia J? Smit lith Hanhart imp CONURUS RUBRITORQUIS ‘ a Be eee oe + oF Js ee 5 Cer 4 day” 1886.] MR. OGILBY ON AN UNDESCRIBED PIMELEPTERUS. 539 CoNURUS RUBRITORQUIS, sp. nov. (Plate LVI.) Green: white of throat and collar only slightly apparent ; at the back of the neck bright red; eye-region naked ; billand feet whitish. Whole length 11°5 inches, wing 5:0, tail 4°7. Hab. South America or West Indies. Obs. About the size of C. enops, but distinguished by its red throat and green under wing-coverts. 4. On an undescribed Pimelepterus from Port Jackson. By J. Doucias Oeitzy, Department of Fishes, Aust. Mus. Sydney. (Communicated by F. Day, C.LE., F.Z.S.). [Received November 1, 1886.] PIMELEPTERUS MERIDIONALIS, Sp. Nov. Bev. 1. 10-2. A. 3/10. V. t/a. Po i7.. C. U7, Te late 57-59. L. tr. 10/19. Cee. pyl. ca. 460. Vert. 11/15. Length of bead from 4°85 to 5:15, of caudal fin from 4°66 to 5°00, of pectoral fins from 7:00 to 7:20, height of body from 3-00 to 3°20 in the total length. Eyes: diameter from 4°00 to 4°50 in the length of the head, from 1°60 to 1°75 in that of the snout, and from 2°00 to 2°30 in the convex interorbital space. Body oblong, com- pressed ; a transverse rounded protuberance in front of the eyes. Cleft of mouth small and transverse; upper jaw rather the longer ; the maxilla reaches to below the anterior margin of the orbit. Pre-, sub-, and interopercles entire. Teeth: a single row of strong curved conical teeth in each jaw, the horizontal portion of which is of equal length with the vertical; behind these rows are narrow bands of similar but much smaller teeth, which probably are intended to finally replace the outer row; vomer, palatines, and tongue densely crowded with minute teeth’. ins: dorsal spines of moderate strength, increasing in length to the seventh, which is about one half the length of the head, and much longer than the rays of the dorsal, though only equal to the first anal ray. Pectorals rounded, rather longer than the ventrals, and from two thirds to three fourths the length of the head. Third anal spine longest and strongest; caudal emarginate. Scales feebly ctenoid, extending in front of the eyes; much smaller on the head; 18 between the bases of the ventrals and the lateral line, and 8 between that and the base of the sixth dorsal spine; those below the lateral line larger than those above it. Pseudobranchie well developed. Gill-rakers 20. Colours dull brownish grey, with a silvery shade below; upper part of head darkest ; all the fins dark. Irides a mixture of orange and silver. 1 In connection with the dentition of Pimelepterus, I may mention that Girella tricuspidata has a small patch of palatine teeth. Dr. Giinther (Cat. i. p. 427) states that ‘“‘in one species there is a short series of palatine teeth,” but e omits mentioning which species possesses this series. 540 MR. G. A. BOULENGER ON [Dec. 7, The examples from which this species is described measure respectively 25°10, 26°10, and 28°30 inches, and were all taken in Port Jackson, where this species is locally known as the “Drummer” ’. I have never seen a small specimen of this fish. Breeding: ouly one, the largest of my specimens, showed any signs of breeding ; this was a male with the milt but little developed ; all three were taken during the month of August. As food: not held in any estimation, and commanding no sale in the market, nevertheless it is, in my opinion, quite equal to the other herbivorous Sparoids. Habits: in these it is a true rock-fish, dwelling in the crevices and indentations of our rocky shores, where it finds abundant food and shelter; it is not given to roaming, and is only taken by the trammel, one end of which is attached to the shore, against which the mesh must actually lie, or else the fish would assuredly pass inside, whence it happens that this species is almost always caught within a few feet of the shore. Note.—From Dr. Ramsay’s MS. notes on Australian Fishes, I find that, so far back as 1881, he noticed these differences with regard to the dentition, but never published any communication thereon. 5. On the South-African Tortoises allied to Testudo geometrica. By G. A. BouLencrER. [Received November 2, 1886. ] (Plates LVII. & LVIII.) Upon the suggestion of the Rev. Mr. Fisk, of Cape Town, who has enriched the Society’s Menagerie with so many interesting Reptiles, I have undertaken a reexamination of the South-African Tortoises allied to Testudo geometrica, and am able to distinguish as many as seven well-marked species, of which the diagnoses follow. The specimens named 7. ¢rimeni, after the Director of the South- African Museum, and 7’, fiski, were lately exhibited in the Society’s Gardens, and were unrepresented in the Natural History Museum. That named 7’. smithi, after the author of the ‘Illustrations of South-African Zoology,’ is established on a specimen erroneously referred by Gray to 7. verreauaii. The true 7’. verreaucii being still unrepresented in our collections, its diagnosis is compiled from Smith’s description and figure. 1 Tt shares the name with Girella elevata, Macleay, and Pachymetopon grande, Giinth. In the ‘ Annals and Magazine of Natural History’ for November 1886, Dr. Giinther described Pimelepterus, sydneyanus, nu. sp., from Port Jackson, and suggested that Pachymetopon grande (Cat. Austr. Fish. i. p. 106) may be Pime- lepterus fuscus, Lacépéde, and that Pachymetopon squamosum, Macleay and Alleyne (Proc. Linn. N.S. Wales, i. p. 275, pl. ix. f. 1), may be Pimelepterus cinerascens, Forsk,, or P. tahmel, Rippell. 1886. ] SOUTH-AFRICAN TORTOISES. 541 1. Testupo Geometrica, L. Beak strongly hooked. No large tubercle on the hinder side of the thigh. Lateral marginal plates not forming an angle with the costals. Nuchal longer than broad. Suture between the gulars longer than that between the anals; suture between the humerals as long as that between the femorals, and much longer than that between the pectorals. Carapace black, with yellow areolze from which yellow rays radiate ; eight or twelve yellow rays on the vertebrals, nine to twelve on the costals, two to four on the marginals. Plastron brown and yellow, the two colours forming more or less ill-defined rays. Common in the Cape Peninsula. 2. Testupo TENTORIA, Bell. Beak strongly hooked. An enlarged tubercle on the hinder side of the thigh. Lateral marginals usually not forming an angle with the costals. Nuchal minute. Suture between the gulars as long as, or shorter than, that between the anals; suture between the humerals longer than that between the pectorals or the femorals. Carapace black, the centre of the areolz with a small yellow or orange spot, from which narrow rays of the same colour radiate ; eight to twelve rays on the vertebral, twelve to fourteen on the costals, three or four on the marginals. Plastron brown in the middle (inner half of abdominal plates), yellow on the sides. Common at Beaufort West. 3. TESTUDO TRIMENT, sp. n. (Plate LVII.) Beak very feebly hooked. No enlarged tubercle on the hinder side of the thighs. Lateral marginals forming an angle with the costals, a convex border with a well-marked longitudinal groove. Nuchal minute. Suture between the gulars as long as, or shorter than, that between the anals ; suture between the humerals not, or but little, longer than that between the pectorals or the femorals. Carapace black, with broad yellow or orange rays radiating from a smali spot on the areolee; five or six rays on the vertebral plates, and four to eight on the costals; a yellow spot or streak at the junction of two plates; one or two rays on each marginal. Plastron dark brown in the centre, with yellow rays, yellow on the sides. Length of carapace of adult 105 millim. Mouth of the Orange River. 4, TESTUDO VERREAUXI, Smith. Beak very feebly hooked. No enlarged tubercle on the hinder side of the thighs. Lateral marginals forming an angle with the costals. Nuchal well developed, a little longer than broad. Suture between the gulars as long as that between the anals; suture between the humerals much longer than that between the pectorals or the femorals. 542. MR. BOULENGER ON SOUTH-AFRICAN ToRToIsES. [ Dec. 7, Carapace dark brown, each dorsal and costal plate with four or five yellow rays proceeding from the yellow areole. Plastron yellow, dark brown in the middle. Near the sources of the Orange River. 5. TESTUDO SMITHI, sp. n. Beak feebly hooked. A large tubercle on the hinder side of the thighs. Lateral marginals not forming an angle with the costals. Nuchal longer than broad. Suture between the gulars nearly as long as that between the anals; suture between the humerals much longer than that between the pectorals or the femorals. Carapace dark brown, with radiating, narrow, yellow, black-edzed rays, meeting in the centre of the areole; plastron yellow, with dark brown rays, the brown predominating in the middle. Length of carapace of adult 115 millim. A single specimen, with the mere indication “S. Africa.” 6. Testupo FIsKI, sp.n. (Plate LVIII.) Beak feebly hooked. A large tubercle on the hinder side of the thigh. Taieha} marginals not forming an angle with the costals. Nuchals small, equilateral. Suture between the gulars shorter than that between the anals; suture between the humerals much longer than that between the pectorals or the femorals. Carapace with brownish-yellow and black rays of nearly equal width, radiating from the yellow areole; six black rays on each vertebral and costal plate, and two on each marginal ; the anterior and posterior pair of black rays on the costal and vertebral plates meeting their fellows form three series of ocelli. Plastron dirty yellow, brown in the middle. Length of carapace of adult 75 millim. A single male specimen, from De Aar, not far from Hopetown, was presented alive to the Zoological Society by Mr. Fisk. 7. TESTUDO SEMISERRATA, Smith. Beak strongly hooked. A large tubercle on the hinder side of the thighs. i ated marginals not forming an angle with the costals; anterior and posterior marginals forming a strongly serrated edge. Nuchal longer than broad. Suture between the gulars as long as, or longer than, that between the anals; suture between the humerals much longer than that between the pectorals or the femorals. Carapace with brownish-yellow and dark brown or black radiating rays, usually of nearly equal width, six to ten in number on the ver- tebral and costal plates. Plastron yellowish, with dark brown rays. Carapace of adult 115 millim. Common in the districts between Latakoo and the Tropic of Capricorn. = NUNN Omit del et hth cS J J. Smit del et lith. Mintern Bros. imp TESTUDO FISKI. 4 ’ hi i t r ’ , s 1886.] ON THE SKULL OF THE CHAMELEONS. 543 6. Remarks on Prof. W. K. Parker’s paper on the Skull of the Chameleons. By G. A, BouLencER. [Received November 25, 1886.] I wish to call attention to what I believe to be a serious error in Prof. Parker’s paper on the Skull of the Chameleons, printed in the last volume of the Society’s ‘Transactions’ (vol. xi. p. 77, 1881). The adult skulls of two species are described and figured, viz. that of Chameleo vulgaris (pl. xvi.) and that of C. pumilus (pl. xix.); but, through some error, the skull of a newly born C. pumilus is represented (pl. xv.) as that of the common species; and as the facts derived from this wrongly-identified species are the basis of the author’s arguments, his conclusions receive, in some points at least, a severe shock from this discovery. Any one will, I think, on comparing the figures, recognize the mistake now that attention is drawn to it, and it is incomprehensible that, although Prof. Parker’s paper has often been quoted during the five years which have elapsed since its publication, it should not have been noticed before. No wonder the author states that he knows “ of no skull whatever in which the roof-bones undergo so great a transformation as in this (C. vulgaris)” or that he should be struck by the resemblance of the adult C. pumilus to the young C. vulgaris, regarding the one as representing a sort of arrested development of the other. I have besides no doubt that he is wrong in his interpretation of the three bones forming the roof of the casque. As recently suggested by Baur, the critical bone ‘ pa- rietal,”” Parker, should be regarded as the supratemporal, and the ‘*interparietal,” Parker, as the parietal. That the three bones are perfectly distinct in the young C. pumilus is well shown on pl. xv. fig. 3, and it is not surprising that the sutures should have dis- appeared on a skull in which the ossification is so expanded, roofing over, as it does, the supratempora! fossee, and studded with tubercles, as is the case in the adult C. pumilus. The statement that the skull of the latter species is less aberrant than that of the common one is therefore incorrect. Should further proofs be required, beyond the inspection of Prof. Parker’s own plates, to establish my identification of the species figured, I might add that the separation of the pre- from the post- frontal is a character of C. pumilus, and that the specimen, received from Mr. Moore, of Liverpool, was no doubt one of a brood, in the possession of Lady Cust, which was born alive in November 1868, and on which Mr. Moore reported at the time (cf. Proc. Lit. & Phys. Soc. Liverp. xxiii. p. 49). Now, it is well known that C. vulgaris is oviparous, and the fact that C. pumilus is ovovivi- parous was recorded as early as 1825 (cf. Kaup, Isis, 1825, p- 992). 544 MR. O. THOMAS ON LAGORCHESTES FAscraTus. [ Dec. 7, 7. On the Wallaby commonly known as Lagorchestes fasciatus. By Otprietrp Tomas, Natural History Museum. [Received November 3, 1886.] (Plate LIX.) One of the earliest known of all the Australian Marsupials was the beautiful little banded Wallaby which was discovered in 1804 on the islands in Shark’s Bay, Western Australia, by Péron and Lesueur, during their famous voyage round the world, and described by them in 1807 under the name of “ Kangurus fusciatus’’’. This species was included by all the earlier writers, with the rest of the Macropodida, in the single genus then recognized, whether called Kangurus, Macropus, or Halmaturus. In 1842, however, it was placed by Gould, on the authority of the typical specimens in the Paris Museum, in Gray’s genus Bettongia, although in the same year he described two other specimens of it as ‘‘ Lagorchestes albipilis,” thus referring them to the genus made by him just pre- viously for the true Hare-wallabies, of which Lagorchestes leporoides is the type. Gould’s two mistakes in referring Péron and Lesueur’s species to the Hypsiprymnine genus Beétongia, and in separating ‘‘ L. albipilis” from it, were corrected by Waterhouse in his excellent general work on the Marsupials, where the species was described * under the name of Macropus (Lagorchestes) fasciatus*—an identification accepted by Gould in his ‘Mammals of Australia,’ where the species is figured as Lagorchestes fasciatus, by which name it has since been generally known. The teeth, as well as the external characters, of L. fasciatus were described and figured by Waterhouse, and their differences from those of the true Hare-wallabies noted; but he does not seem to have at all appreciated the importance of these differences, which appear to me to be so great as to compel me, 80 years after the first description of the species, to form a new and special genus for its reception. -This genus I propose to call Lagostrophus*. The differences in dentition between Lagorchestes and Lagostro- phus are not of the trivial and unimportant nature of those charac- teristic of most of the other genera of this very homogeneous family, but are of a kind to show that Lagostrophus fasciatus must have not only different food, but even a different manner of eating it to any of the other members of the subfamily Macropodine. On examining the incisors of any of the ordinary Kangaroos and Wallabies (Plate LIX. figs. 8, 9, and 12), we find that the whole set form a widely open curve, and that the sizes and proportions of the 1 Voy. Terres Austr. i. p. 114, Atl. pl. xxvii. 2 Vol. i. p. 87 (1846). 3 Nat. Hist. Mamm. i. p. 87 (1846). 4 Nays, a Hare, and orpogos, a band or belt. 1886.] | MR.O THOMAS ON LAGORCHESTES FASCIATUS, 545 individual teeth are more or less as follows :—i’ is the largest of the three, boldly curved forwards, and descending below the level of the other two, its tip sharp and gauge-shaped; i° andi’ are both much smaller than i', very narrow transversely, and provided with sharp cutting-edges ; of the two, i° is nearly invariably the larger. On . placing the mandible iv position, the large scalpriform lower incisors fit in naturally between the upper ones, not biting vertically upon their edges, but only upon the palate between them (fig. 9). The lower incisors themselves are very uniform in shape, and always provided with sharp cutting-edges along their inner margins (see the section fig. 10), the animals being able, owing to the looseness of the symphysial joint, to separate and approximate these cutting-edges’, and thus to utilize them as a pair of scissors with which to snip off leaves or grass, Turning, on the other hand, to Lagostrophus fasciatus, we find a very different state of things. First, the two series of upper incisors are close together, meeting at a sharp angle in front and diverging but little behind (fig. 2). Then as to the size of the teeth, i’, instead of being the largest, is the smallest of the three, at least in cross section, and even vertically it is but little longer than the others (figs. 2 and 6); in shape it is conical, scarcely curved forwards, and with a blunt, rounded or flattened tip. I? and i° are each longer antero-posteriorly than i* and, when looked at externally, have much the same appearance as those of Lagorchestes, except that i is longer than i*, while in Lagorchestes and in nearly all other Kangaroos the reverse in this case. But when looked at from below (fig. 2), there appears a very remarkable difference ; instead of being narrow and sharp-edged, they are broad and flat-topped, and are evidently not formed for cutting in the true sense at all. The palatal surtace of i forms an even oblong, its breadth slightly more than half its length ; while the flatness of i° is only modified by a broad shallow groove running along its centre, and terminating at its postero-external corner, where it forms a notch on the outer edge of the tooth evidently homologous with that found in a similar position in the other Wallabies. Trying now the same experiment as before of placing the lower jaw in position, we see at once what a difference the contraction of the incisor series must make in the manner of using them; for the lower incisors, instead of dropping down between the upper ones, come flat upon the top of them, so that there can only be a grinding- and not a cutting-action between the upper and lower teeth, An examination of the lower jaw of L. fasciatus seems to show that this species, and this alone of the Macropodine, is without the power of using the two rami independently, as the junction between them, instead of being loose and narrow, is broad, close, and firm, the vertical height at the symphysis being so great in proportion to the size of the jaw as to produce a distinct rounded prominence on 1 See Murie and Bartlett, P. Z.S. 1866, p. 28. Proc. Zoon. Soc,—1886, No. XXXVI. 36 546 MR. O. THOMAS ON LAGORCHESTES FAsciatus. [Dee. 7, its lower side corresponding to the chin, no trace of such a prominence being present in any of the other genera. Tal natural correlation to this structure of the jaw, the lower incisors themselves have not the sharp inwardly projecting edges characteristic of those of the other Kangaroos, and are merely approximated to each other by their flat inner surfaces; the trans- verse sections of the incisors of the two forms (figs. 4 and 10) show this difference better than any description. The incisors and symphysis thus indicating a difference in the motion and use of the mandible, we should naturally expect an appreciable change in the shape of those parts of it by which it is attached and moved, and we therefore find, first, that the coronoid process possesses the very unusual character of having its anterior edge slightly concave in its upper half, all other Kangaroos having iis part evenly convex ; and, secondly, the condyle, Instead & having its length and breadth much about equal, is very much broader than long, and is provided with a broad, flat, supplementary internal process (compare figs. 5 and 11). Canines, present in Lagorchestes, are, as in the majority of the Macropodide, wholly absent in Lagostrophus. The two premolars of Lagostrophus, i. e. the smaller anterior deci- duous one, pm’ of the typical dentition, and the larger permanent one, or pm* (fig. 7), are both broad and flattened, their posterior decidedly greater than their anterior diameters, with well-developed internal edges, and with four or five shallow vertical grooves on their external surfaces. The premolars therefore correspond with the incisors in being broader and more flattened than is usual ; but the difference, at least in comparison with certain of the broader-toothed species, such as Macropus brachyurus, Quoy and Gaim., or Lagorchestes conspicillatus, Gould, is by no means so striking as in the case of the incisors. The molars appear to be precisely similar to those of Lagorchestes and the other smaller members of the Macropodine. The general shape of the skull (fig. 1) presents nothing very remarkable, except that, owing to the approximation of the two incisor series to each other, the premaxillee bearing them are very much narrower transversely than usual, and therefore give a peculiar slender and pointed appearance to the muzzle. With regard to the external characters, we have first to note that the rhinarium, notwithstanding the statements of Gould and Water- house, is really practically naked, as in the Wallabies, and is not hairy as in Lagorchestes*. The hair, in fact, only grows down the centre of the nose to the level of the superior internal angle of the nostrils, leaving the whole of the front of the nasal septum bare. The hind feet, instead of being short-haired as in Lagorchestes, are covered with long bristly hairs, very much as in Petrogale, these hairs nearly entirely covering up the narrow naked sole, and hiding the short, but strong and conical, central hind claws. ? Even in Lagorchestes the hairiness is very variable, L. conspicillatus having a yery much less hairy muzzle than L. /eporotdes, the type of the genus. % Giaud Horman-Fisher del et lich Mintern Bros. ump LAGOSTROPHUS FASCIATUS, FIGS. - o le 1|_—¥ LAGORCHESTES .LEPOROIDES, IGS. 8-12. 1886.] MR. 0. THOMAS ON LAGORCHESTES FASCIATUS. 547 Finally, so far as regards colour, the transverse banding of the lower back presents a style of coloration quite unique in this family, and, beyond the Macropodide, only found among Marsupials in Thy- lacinus and Myrmecobius, in which, however, it is far more prom- inent than in the Banded Wallaby. The last point for consideration is the systematic position of Lagostrophus among the other genera of the family, and I have therefore compared its characters with those of the sections and groups into which Prof. Garrod, in his classical paper on Dorcopsis *, has divided the subfamily Macropodine. ‘This comparison shows that the differential characters of Lagostrophus are of distinctly greater systematic importance than are those separating Prof. Garrod’s Section I. from Section IT., as these appear to be by no means so persistent or invariable as that author supposed. I cannot therefore consider Lagostrophus, as a group, less than equal in value to all the other genera of the subfamily combined, so that the following is the arrangement that I would propose to substitute for Prof. Garrod’s :— Family MACROPODIDA. Subfamily Macroropinz. Section I. A. Genera Macropus, Petrogale, Onychogale, Lagorchestes. B. Genera Dendrolagus and Dorcopsis. Section II. Genus Lagostrophus. Subfamily HypstpRYMNIN2. Section I. Genera Hypsiprymnus, Bettongia, depyprymnus, Subfamily HyesipRyMNODONTINE. Section I. Genus Hypsiprymnodon. EXPLANATION OF PLATE LIX. Lagostrophus fasciatus, upper view of skull. , palatal view of upper incisor teeth. le W< —— ——,, palatal view of upper incisor teeth, with the lower jaw in position. —— ——, outline of transverse section of the two lower incisors. , right condyle of lower jaw. , side view of upper and lower incisors. , palatal view of ee and lower incisors. . Lagorchestes leporoides, as in fig. 2. , as in fig. 3. , as in fig. 4. , as in fig, 5. ——.,, as in fig. 6. Fig. 1 is of the natural size; all the others are magnified three times. Fig. POATD OR Coho es 11. ——- 1 p, Z.8. 1875, p. 58. 548 PROF. R. COLLETT ON PHASCOLOGALE VIRGINIE. [ Dec. 7, 8. On Phascologale virginia, a rare Pouched Mouse from Northern Queensland. By Rosert Cottett, C.M.Z.S. [Received December 2, 1886.] (Plate LX.) PHASCOLOGALE VIRGINIZ, De Tarragon, 1847. (Plate LX.) Phascologale virginia, De Tarr. Revue Zool. 1847, p. 177. Diagn. Skull with strong sagittal and occipital crests, and distinct processus postorbitales. Incisors almost equal; upper canine very long. First premolar very small; third the largest. Ossa palatina with foramina; pars ner ion scarcely inflated behind the bulle. Ears large, almost naked; tail as long as the body and head, scantily clothed with adpr essed hairs. Hind feet slender, hallux very short; sole of metatarsus naked in the middle line ; tubereulated callosities at the base of the toes. Colour blackish, grizzled with silvery white ; head reddish grey, with a black stripe from nose to between the ears, and trace of another on the side of the snout. Below greyish ; feet pale red, tail reddish grey with black tips‘. Measurements, taken from the stuffed specimen :— millim. Length of body (with head) .......... about 125 Length of tail........ sie kee ee ae e 120 From tip .erenout to .¢ar 005. 5 dy oie kiasiy: ss ee re Height of ear, exterior margin.............. 20°5 Height of ear, interior margin........ S's faba pf Sole of hind foot (with claw) .............. 33 Fur rather short, not woolly; each hair bluish grey at the base, the outer third white with black tip, some hairs entirely black. Feet slender; point of hallux not nearly reaching to the base of the toes. Skull, The skull is strongly built, with high sagittal and occipital crests, and a distinct processus postorbitalis ; the dentition is, how- ever, comparatively weak. millim Lprigtl sot See iat fic ego mt immnie = papel + sows (ele Breadth across arcus zygomaticus i cetaaris =) cane rade 19 Peicht...2: Ghee eae Ysa ae Wace paral e Shortest breadth between orbits .. Sto] Mt tees Breadth before the commencement of a. zygomaticus. 12 Length of tooth-series in upper jaw.............- 15 Length of tooth-series in lower jaw.............. 13 Dentition :—I. 4; C.;; P. 3; M. 4 (46). 1 The colour of the tail and snout is rather indistinct, the hairs being very much worn, » ¥ = as i OS pia ay ie ‘ = . 1 s : : 7 j p. ‘ . 5s £ ‘ . . ' * : ‘ F . oath 1886.] THE SECRETARY ON ADDITIONS TO THE MENAGERIE. 549 In the upper jaw the first incisor is short, and almost imper- ceptibly larger than the other incisors. Canine long and curved. The premolars form an almost unbroken series with the canine and first molar. First premolar very small, scarcely higher than fourth incisor; second a little larger; third premolar the largest, the middle cusp being as high as the molars. The molars are rather feeble, with relatively low crowns and blunt cusps; last molar very narrow. In the lower jaw the canine is a little shorter than that in the upper. Fourth molar only alittle smaller than third. Incisors and premolars as in upper jaw. Compared with Ph. minima the brain-case is higher, but narrower, and the arcus zygomaticus longer. Ph. apicalis has larger bulle ossee, but shorter foramina incisiva; the third premolar in that species is almost rudimentary, and the second premolar larger than the two other premolars together. In both these species the crests on the brain-case are scarcely developed, and the postorbital pro- cesses wanting. Hab. Herbert Vale, Northern Queensland ; one specimen, a full- grown male, collected by Dr. Lumholtz, January 1883, is preserved in the Zoological Museum at Christiana. The specimen was dug out from a hole in the ground, and its habits seemed not to be arboreal’. Christiania, 15th November, 1886. EXPLANATION OF PLATE LX. Fig. 1. Phascologale virginia, natural size. 2. Skull, natural size. 3. Canines and premolars, three times natural size. December 21, 1886. Prof. Flower, LL.D., F.R.S., President, in the Chair. The Secretary read the following report on the additions to the Society’s Menagerie during the month of November 1886 :— ‘Che tctal number of registered additions to the Society’s Mena- gerie during the month of November was 166, of which 64 were by presentation, 22 by purchase, 16 by birth, 4 were received in ex- change, and 60 on deposit. The total number of departures during the same period, by death and removals, was 107. 1 My friend, Mr. Oldfield Thomas, informs me, on the authority of M. Huet, of Paris, that the original type of this species, the locality of which was un- known, appears to have been lost; and as the animal has been overlooked ever since its first description, I have thought it worth while to figure and redescribe it from the beautiful specimen obtained in Queensland by Dr. Lumholtz. 550 MR. H. SAUNDERS ON A HYBRID DUCK. [ Dec. 21, Mr. Howard Saunders, F.Z.S., exhibited on behalf of Mr. R. J. Howard, of Blackburn, a specimen of a hybrid between the Tufted Duck (Fuligula cristata) and the Pochard (#. ferina), bred in Lancashire; and read the following extract from a letter addressed to him by Mr. Howard on the subject, dated Fern Bank, Blackburn, Oct. 28th, 1886 :— “7 have forwarded for your acceptance a hybrid between the Pochard and the Tufted Duck, knowing that an authenticated specimen will be of interest ; for I suppose I must take it for granted that the bird referred to by you in the 4th edition of ‘ Yarrell’ (vol. iv. p. 433) as ‘apparently a hybrid between the Tufted Duck and Pochard’ is the only one known to you. *¢ A pinioned pair of Pochards first bred at Woodfold Park in 1882, since which date several broods have been annually reared there (‘ Yarrell,’ vol. iv. p. 414). I found the Tufted Ducks nesting on the same reservoirs in July 1884, some of the young birds being sub- sequently captured, pinioned and turned down again (ibid. p. 431); the first recorded instance of the breeding of the Tufted Duck in Lancashire. The birds of both species leave the reservoirs during the severe weather of winter. “On the 9th of May last, I saw a male Pochard apparently paired with a pinioned female Tufted Duck. On the 23rd of the same month two male and one female Tufted Ducks appeared ; the male Pochard would not allow the male Tufted Ducks near the pinioned female, but drove them off if they approached within 30 or 40 yards. Soon after this all the drakes left, and I saw little of the ducks until the 20th June, when both appeared on the water; the full-winged female Tufted Duck with a brood of 9, the pinioned one with 10 young hybrids. “From the first I could easily distinguish the pure-bred young from the hybrids: the upper parts of the former being uniform umber-brown, whilst the latter had the cheeks and throat buff. As the birds began to feather, I noticed that the hybrids were bulkier, the general appearance being more that of the Pochard than of the Tufted Duck ; the head, neck, and upper surface were of a much lighter and warmer brown, the feathers about the base of the upper mandible rather lighter-coloured than the rest of the head, but not showing a distinct patch as in the Tufted Duck. We caught two hybrids on the 30th July, and put them on the reservoir in the Blackburn Corporation Park ; and on the 2nd August I sent two, in the name of Mr. Thwaites (to whom I am indebted for permission to deal with the birds as I wish), to the Zoological Society’s Gardens. Their description is as follows, the sex being uncertain :—Length 15°5 and 15 in.; bill dark blue, almost black, 1-6 in. in length, and a trifle more dilated towards the point than in the pure Tufted Duck ; irides yellowish brown ; legs and toes blue, darkest at joints, webs black. Two of the young Tufted Ducks, male and female, caught on the 3lst July: length 14°5 and 14 in.; bill black, 1*5 in. in length ; irides dull yellow; legs and toes as in the above hybrids. “The bird which I sent you was shot on the 19th August, beg 1886. ] MR. J. B) SUTTON ON ATAVISM. 5oL then strong on the wing, and proved, on dissection, to be a male. Those which I put on the reservoirs in our Corporation Park do not appear to have changed i in plumage ; there is not as yet the slightest sign of a crest.’ The above rare hybrid has since been presented to the British Museum of Natural History. The following papers were read :— 1. On Atavism. A Critical and Analytical Study. By J. Buanp Surton, F.R.C.S., Lecturer on Comparative Anatomy, Middlesex Hospital, Erasmus Wilson Lecturer on Pathology, Royal College of Surgeons. [Received October 22, 1886.] In aninteresting paper entitled “ Critical Remarks on Polydactyly as Atavism,’’ Gegenbaur enters into a masterly discussion of this confessedly difficult subject, and, in the course of summing-up, he ventures to divide atavistic phenomena into two groups—PaL«£o- GENETIC and NEOGENETIC. Atavism he defines as “‘a re-appearance of a more primitive organization, or a reversion (Riickschlag) to a primary state.” To choose an example :—the occasional presence of an os centrale in the adult human carpus is a reversion to a condition very prevalent in the lower Mammalia. We know that a cartilaginous representative of this ossicle is easy of detection in the embryo; but Atavism does not consist in the existence of a latent germ, but in its becoming perfected and further developed. In this case the atavistic part exists, by law of inheritance, in the early embryo as a germ which normally disappears, but in some cases becomes further developed. This is Gegenbaur’s Palzogenetic Atavism. If the abnormal part (using the term abnormal in its most literal sense) is not found as a germ in the embryo, the reversion is “* Neogenetic.”” My object is to show that all examples of atavism belong to the Palzeogenetic group and that Neogenetic Atavism has no existence. The question of polydactyly I do not intend to discuss, but shall select the foot of the Horse, as Gegenbaur has done, to serve as illustrations of the principle, and thence extend the view broadly. The descent of the modern Horse from five-toed ancestors is beyond all question. That the animal of to-day walks on an enlarged third digit with a rudimentary digit on each side in the manus and pes is accepted doctrine. The comparative recent ances- tors of the Horse were tridactyle. Gegenbaur states that Hensel’s* ? Morph. Jabrbuch. Bd. vi. 8. 584-596, A translation by Drs. Garson and Gadow is given in ‘ Journal of An: atomy and Physiology,’ vol. xvi. p. 615. 2 “Ueber Hipparion mediterraneum.” Abk. k. Akad. d. Wissensch. z. Berlin, 1861, S. 66. 552 MR. J. B. SUTTON ON ATAVISM. [ Dec. 21, investigations point to the probability that the finger typically attached in Hipparion to the medial styloid bone was the last to abort. It is certainly noteworthy that in the majority of cases of polydactyly occurring in Horses it is this digit which reappears most frequently. In the Teratological Gallery in the Museum of the College of Surgeons several specimens of Horses’ feet are shown with a well- developed second digit. Cheauveau figures * a specimen preserved in the Veterinary Museum at Lyons; but the most complete case of its kind is that figured and described in Prof. Marsh’s paper* “On Polydactyle Horses, Recent and Extinct.” In this instance the inner digit was present on the four feet. Besides giving an in- teresting account of extra digits noticed by early writers, this eminent paleontologist tells us that the more frequent occurrences of extra digits on the manus is precisely what a study of fossil forms of equine mammals would lead us to anticipate. These cases support the view as Gegenbaur points out, that the atavistic parts do not belong to forms palzeontologically remote or systematically far distant. In the Spider-Monkey the thumb is normally absent, or repre- sented merely by a nodule of cartilage or fibrous tissue. Yet on one occasion J dissected an Ateles paniscus which had on each hand a perfectly developed thumb. This condition is not very uncommon. If the parts be dissected in normal specimens, the thumb is repre- sented by a band of cartilage and fibrous tissue attached to the trapezium. The illustrations which have been used were selected merely to give a clear notion of genuine Atavism—the palogenetic form. The question of polydactyly is in some instances susceptible of another explanation, which I do not propose to speak of in this paper. Atavism in relation with the Prostate. Leaving the skeleton, attention wiil now be invited to a re- markable instance of Atavism presented by the prostate. In struc- ture and intrinsic relations this organ presents some exceptional features. It is best regarded as a capsule composed of fibrous and unstriped muscular tissue, mixed with tubular glands, surrounding a recess known as the utriculus masculinus. The utriculus separates the termination of the confluent ducts of the vesiculze seminales and vasa deferentia, whilst it is tunnelled near its anterior aspect by the commencement of the urethra. The glands of the prostate are best considered as tubular alveoli which unite into a smaller number of excretory ducts (about twenty) opening in two depressions of the urethra known as the prostatic sinuses. The tubules are lined by columnar epithelium. The central recess before mentioned has been named the sinus } «Anatomie Comparée.’ 2 American Journal of Science and Art, yol. xvii., June 1879. 7]? 1886. } MR. J. B. SUTTON ON ATAVISM. 553 pocularis, utriculus, or uterus masculinus. Usually it is nearly half an inch long, and opens by a narrow slit in the middle of the caput gallinaginis. It is lined by mucous membrane continuous with that of the urethra, and covered by stratified epithelium. Some small tubular glands open on the free surface of the mucous membrane. This utriculus is of great interest morphologically, as it represents in the male a persistent portion of the confluent segment of the Miillerian ducts. Weber regarded it as corresponding with the uterus, but Leuckart showed that a part of it must be looked upon as representing the vagina. My observations induce me to regard the prostate as a suppressed uterus, the fibro-muscular tissue representing the matricial walls, the follicles correspond to the utricular glands, and the utriculus is identical with the cervix uteri and that portion of the vagina immediately adjacent. The evidence in support of this view will now be put before the reader. In order to render every detail in clear light, we must refer briefly to the fundamental structures concerned in forming a func- tional uterus. In the Lizard, in common with the majority of the Sauropsida, the ova are conveyed to the exterior by two muscular tubes lined with mucous membrane, known as oviducts. The eggs, when they escape from the ovaries, are received by the dilated end of the oviduct, known as the infundibulum, and quickly passed onwards ; they receive at the commencement of the journey a coating of albumen. Pushed on by the contortions of the tube, they arrive at the third or uterine portion. Here they receive a coating of calcareous matter known as the shell, and are then ready for expulsion. In these oviducts, with their mucous membranes and glands, we have the fundamental condition of the ducts which in the human embryo conspire to form the uterus with its Fallopian tubes and vagina. In order to clearly describe the manner in which the Fallopian tubes, uterus, and vagina are formed from the Miillerian ducts of opposite sides, each duct may be conceived as made up of three parts :-— The upper third becomes the Fallopian tube; the funnel-shaped and usually fimbriated extremity communicates with the peritoneal cavity. The middle portions of the ducts fuse together, and form the fundus, body, and neck of the uterus, whilst the lower thirds of the Miillerian ducts form a vagina. Such is the commonest arrange- ment. On comparing the parts of this compound organ with the Lizard’s oviduct, it becomes evident that the infundibulum and albumen segment in the bird represent the Mammalian Fallopian tube, the second or uterine portion corresponding with the uterus and vagina of Eutheria. On tracing the homologies closer, we find that the portion ot the bird’s oviduct concerned in secreting albumen corresponds with that portion of the Miillerian duct which forms the fundus and body of .the uterus; and the utricular glands, which are coucerned in 554 MR. J. B. SUTTON ON ATAVISM. [Dec. 21, secreting a thick, viscid, albuminous material, are simply modifica- tions of the simple recesses found in the bird’s oviduct. The third, or uterine section of the oviduct, corresponds to the cervix of the uterus and the vagina. To this we shall return. In the male of the higher mammals, theMiillerian ducts by their fusion give rise to the utriculus. This cavity is formed by that portion of the ducts which in the female constitute the cervix uteri and upper segment of the vagina. Excellent confirmatory evidence of this view is afforded by a rare malformation to which the prostate is liable. Instead of the Miillerian ducts disappearing after the posterior portions have fused to form the utriculus, a segment of each may persist, so as to give rise to a bicornuate utriculus, in fact a miniature uterus. In rarer instances a Miillerian duct may persist through its entire length. Such a case has been described by Dr. Ord*. There is good reason to believe that some examples described as double ureters were of this nature. If the human prostate be examined by cutting it into slices in the direction of the urethra, at any age after puberty, but much more easily at fifty years, small brownish or black bodies, usually of the size of poppy-seeds, will be detected. These bodies, familiar as prostatic concretions, are, as a rule, very much smaller in young subjects, in whom it is often necessary to scrape the cut section of the lateral lobes of the prostate, and submit the juice to microscopic examina- tion in order to detect them. Before puberty they are practically absent ; in old age they may attain the dimensions of split peas. In number they may vary from twenty to two thousand; in size from z757 of an inch to that of a cherry-stone ; in colour bright red, brown, or even black. In consistency they may be soft, hard, or even brittle. Chemically they contain organic matter, about one half, the rest being made up of phosphate and a small quantity of carbonate of lime. For a careful and detailed account of prostatic concretions, the student should consult an excellent paper by Sir Henry Thompson, entitled, ‘‘ Some observations on the Anatomy and Pathology of the Adult Prostate ”’ °*. In the preceding pages an endeavour has been made to prove that the cervix of the uterus and contiguous portion of the vagina correspond to the shell-forming segment of the bird’s oviduct. The prostate and utriculus correspond to the uterine cervix and upper part of the vagina, therefore they are homolegous with the shell- forming segment of the bird’s oviduct. The shell of an egg consists of animal matter impregnated with salts of lime, and is due to the activity of the glands in the third section of the oviduct. Prostatic concretions are due to the activity of the glands lodged in the prostate. The inference is clear that prostatic concretions and egg-shells agree structurally and chemically, and are produced by homologous organs. ‘Thus man has in his 1 Medico-Chir. Trans, vol. lxiii. p. 11. 2 Medico-Chir. Trans. vol. x]. p. 78 (1857). heh 1886. | MR. J. B. SUTTON ON ATAVISM. 555 prostate an unimpeachable witness of an ancestry with the feathered tribe, low down among the oviparous reptiles. Let me now proceed to show how very little information we possess concerning latent germs which may be present in the embryo. For example, the discovery of the germ of an os centrale in the carpus of man was certainly startling. Yet its existence might have been anticipated from what we know of the variations in the number of the carpal ossicles in the adult. Atavism drew the attention of anatomists to a secondary astragalus in the human tarsus, and Barde- leben succeeded in detecting the germ. (This has been questioned by Baur, but his objections are inconclusive.) We must now consider some cases of a different character. Atavism in relation to Secondary Sexual characters. As Darwin points out}, two distinct elements are included under the term “inheritance ’’—the transmission and the development of characters. The distinction is a most important one, especially in its bearing on the question of Atavism, that the two conditions will be illustrated by concrete examples. In most species of the Deer tribe it is the rule for the male alone to possess antlers, yet it is a well attested circumstance that under certain diseased conditions of the sexual organs, especially atrophy or degeneration of the ovaries, rudimentary horns which are never shed appear in the female. This shows us that although the female is in possession of the secondary sexual organs in virtue of transmission, yet they remain latent as a rule, and only become developed under extraordinary circumstances. The same holds good for those cases of hens who for years lay eggs, yet eventually cease to do so, put on one side the plumage proper to their sex, and adopt more or less completely the plumage of the cock. These examples open up the subject of secondary sexual charac- ters. The question of primitive hermaphroditism has been already discussed in a preceding paper, and an attempt was made to show that, for a brief period at least, the embryo presents sexual parts common to the male and female, so that for a time it is absolutely impossible to determine the sex. What is true of the embryo applies equally to animals normally hermaphrodite: no distinctive charac- ters are displayed externally. Also in cases of hermaphroditism occurring in animals normally bisexual, the secondary sexual charac- ters are intermediate to those of the functional male and female. It is therefore fairly evident that the female, though she differs from the male in the non-development of secondary sexual characters, yet possesses them in a latent condition; or, to put the matter briefly, they are transmitted, but not developed. ‘This raises two questions, each of equal importance :—(1) How are these characters transmitted? (2) What hinders their development? It seems to me that the second of these questions is the one with which we are chiefly concerned here, and that the non- development of 1 «Descent of Man,’ 2nd ed. p. 227. 556 MR. J. B. SUTION ON ATAVISM. [ Dee. 21, secondary sexual characters can be explained on the principle known as the “ Correlation of Organs.” In order, however, to render this explanation tenable, it will be absolutely necessary to prove, as far as possible, that the germs of secondary sexual organs, which only manifest themselves occasionally in the females of dimorphic forms, are really inherited ; and, if the female is furnished with the germs of these structures, to show by what method they are transmitted. It is to this somewhat intricate part of the question that we niust now direct our attention. If a careful analysis be made of those structures which constitute secondary sexual characters, we shall find that they are almost entirely developed in connection with the integument. The majority— whether they be horns, bristles, spurs, or teeth, for attack or defence ; or exuberance of hair, feathers, wattles, combs, &c., for esthetic purposes,—the integument and the immediately subjacent tissues are responsible for them. In the earliest embryos of most mammals we distinguish at a very early stage two layers of cells, known as the epiblast and hypo- blast. In most of the Metazoa a new layer is interposed known as the mesoblast ; this originates in part from the epi- and in part from the hypoblast. It is the epiblast and the portion of mesoblast immediately adjacent that furnishes secondary sexual organs. From whence is the epiblast derived ? -. We know new that the essential act of impregnation consists in the union of a spermatozoon with an ovum; the head of the spermatozoon constitutes the male pronucleus, the germinal area the female pronucleus. After the pronuclei have united segmentation begins, and the formation of the fundamental layers is quickly brought about. ‘There are good grounds for believing that the initial streak indicating the commencement of segmentation really marks the line of fusion between male and female pronuclei. If we measure the size of the head of a functional spermatozoon, it will be found equal to ,),5 of an inch, whereas the germinal area of the ovum equals =, of an inch. It is a very significant fact that the segments which give rise to the epiblast are smaller than those which furnish the hypoblast and mesoblast; to this there are very few exceptions. This is exactly what might be expected, the halves of a globe z=; of an inch in diameter would certainly be smaller than the halves of a sphere one twelfth the size. The facts at our disposal seem to point to the conclusion that the epiblast is chiefly derived from the male element, while the female pronucleus is responsible chiefly for the hypo- and greater portion of the mesoblast. If this be true, the transmission of characters peculiar to the male is not so obscure as many have supposed. We must now inquire howit is, that if the female possesses all the secondary sexual characters of the male in a latent manner, what is it that prevents them manifesting themselves. When differentiation of sexes occurs in animals previously hermaphrodite, it involves either the loss of certain characters on the 1886. ] MR. J. B. SUTTON ON ATAVISM. 557 part of the female, or the acquisition of new characters by the male, or at any rate increased functional importance of certain organs possessed, when in the state of hermaphroditism, by all the forms. By natural selection the male would acquire (or, if already in his possession in a functional condition, they would become more developed) means for seizing and retaining the female, such as the claspers of sharks, the callous pads of frogs, &c. Paternal duty requires the male to protect the young and defend the females from harm; hence horns, teeth (as in the musk-ox), spurs, tusks, &e. become more developed in him. The duties of the female require her not only to furnish the material out of which the young are to be formed, but in many cases she is required to provide them with nutrition long after they enter the world. The material which the female thus provides is of the very kind necessary, in many instances, to build up such structures as horns, tusks, teeth, and the like. Further, this material is required by the female at the corresponding period of life in which they become developed in the male, viz. on the advent of puberty. We may state with certainty that a distinct correlation exists between the generative organs of the female and the development of the secondary sexual male characters. The more developed and functional the female reproductive organs become, the less likely is she to manifest the secondary characters of the male. It may be argued, that in some cases the female simulates the male, as in the few examples of female Deer possessing horns. Quite true; but so long as the female is engaged in the duties of reproduction, these secondary characters are never developed to the same extent asin the functional male. It must also be borne in mind, that in cases where sterile females, or those which have ceased to bear young, put on external male characters, they rarely attain such proportions or beauty as in the male; for in the males the general excitement produced upon the system by sexual passion has a most powerful stimulant effect upon the growth and development of these structures, which is wanting inthe female. So that in her attempts to emulate the male she succeeds to a certain degree, but rarely, if ever, attains to so good a condition. Hunter has recorded some experiments which have a bearing on this matter :— **j wished also to ascertain if the parts peculiar to the male could grow on the female, and if the parts of a female, on the contrary, would grow on a male. ** Although I had formerly transplanted the testicles of a cock into the abdomen of a hen, and they had sometimes taken root there, but not frequently, and then had never come to perfection, yet the experiment could not, from this cause, answer fully the intended purpose ; there is, I believe, a natural reason to believe it could not, and the experiment was therefore disregarded. I took the spur from the leg of a young cock, and placed it in the situation of the spur in the leg of a hen-chicken ; it took root, the chicken grew to a hen, but at first no spur grew, while the spur that was left on the 558 DR. R. VON LENDENFELD ON THE SYSTEMATIC [ Dec. 21, other leg of the cock grew as usual. This experiment I have repeated several times in the same manner, with the same effects, which led me to conceive that the spur of a cock would not grow upon a hen, and that they were, therefore, to be considered as distinet animals, having very distinct powers. In order to ascertain this, I took the spurs of hen chickens and placed them on the legs of young cocks. I found that those which took root grew nearly as fast, and to as large a size as the natural spur on the other leg, which appeared to be a contradiction to my other experiments. Upon another examination of my hens, however, I found that the spurs had grown considerably, although they had taken several years to do it ; for I found that the same quantity of growth in the spur of a cock, while on the cock, during one year, was as much as that of the cock’s spur on the hen in the course of three or four years, or as three or four to one; whereas the growth of the hen’s spur on the cock was to that of the proper spur of the hen as two to one.” When a female animal belonging to a dimorphic species assumes male characters, it is truly an example of Atavism, or development of transmitted characters normally latent. This part of the matter has been dwelt upon at some length for the following important reason. If we regard the epiblast and the structures developed therefrom as representing the chief cha- racters derived from the male parent, it opens up a field of interesting inquiry in clinical medicine and pathology regarding hereditary diseases, and it demonstrates clearly enough that we have little knowledge concerning the germs of organs which may be latent in an animal; therefore Neogenetic Atavism is, at its best, exceedingly questionable. To assume that such a form of Atavism exists, is to believe in the sudden development of new characters: this is totally opposed to the fundamental principles of Evolution. The question is one of great importance to the pathologist, inasmuch as there is very great probability that many aberrations of organs and tissues are atavistic in their nature. 2. On the Systematic Position and Classification of Sponges. By R. v. Lenpenrerp, Ph.D., F.L.S., Assistant in the Biological Laboratory of University College, London. [Received December 20, 1886.] I. Introductory Remarks, p. 558. IL. Nomenclature of Spicules, p. 559. III. The Systematic Position of Sponges, p. 564. IV. The Classification of Sponges, p. 570. V. Key to the Recent Families of Sponges, p. 589. VI. Appendix. List of Publications, p. 592. I. InrRopuctrory Remarks. Our knowledge of the development and structure of Sponges is of such recent date that we have hardly had time to utilize it for systematic purposes till now. 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 559 Whilst the anatomical and embryological work of recent authors, particularly of F. E. Schulze and his pupils, has made us acquainted with the structure of Sponges in a satisfactory manner, our know- ledge of species, which was formerly practically confined to those from the Mediterranean and the Atlantic, has been greatly extended by the collections made during the voyages of the ‘Alert’ and ‘Challenger’ in all parts of the world, and by my own labours in the Australian seas. I think, therefore, that the time has now arrived to endeavour to establish a classification of Sponges, and to discuss the position which the Sponges, as a group, occupy in the scale of Nature. In an Appendix to this paper a nearly complete list of publications on Sponges is given. It has been made by interpolating old, new, and omitted papers in D’Arcy Thomson’s (1495) list of 551 papers, the references in which have been verified. I must express my thanks to Mrs. v. Lendenfeld and to Mr. A. Dendy for their share in this work, and also to Mr. Ridley for his kindness in allowing us to use his most valuable MS. notes on this subject. In the section on the systematic position of Sponges, the principal views held on the subject are discussed, and reasons are given for considering the Sponges as the first Phylum of the Grade Ccelentera, which arrangement has been adopted in this paper. The main classification of the Orders is the result of my own anato- mical work, and has been arrived at independently of other authors. It affords me much pleasure to state that this classification is, in the main, similar to that established by Vosmaer (1550), although we have arrived at our results in different ways, and our diagnoses differ accordingly. To that section of this paper which deals with the arrangement of the Families and Subfamilies, and the enumeration of the principal Genera, Mr. A. Dendy has contributed the portions relating to the Suborders Clavulina and Halichondrina with the exception of the Tethyde and Chalininee. The portions relating tothe Hexactinellida and Tetractinellida are compiled from the recent papers of Schulze (1369), Sollas (1458), Vosmaer (1550), and Zittel (1639). The remainder is based on my own MS. notes. II. NoMENCLATURE OF THE SPICULES. Various terms for the spicules found in Sponges have been used by different authors. In consequence of this a certain confusion has arisen with regard to the meaning of the terms employed. Vosmaer (1550) made a chivalrous attempt to establish a satisfactory Nomenclature, which, however, has unfortunately not been accepted by recent authors on Sponges except myself, so that it only added to the already existing confusion, Recently Sollas, Ridley, and Dendy have established a new nomen- clature for Monaxonid spicules, which I have agreed to adopt, and which has been used by them and myself. I do not think it perfect, but I am certainly not in a position to replace it by anything better, and therefore adopt and explain it in this paper. Schulze’s nomen- 560 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, clature of Hexactinellid spicules is here, of course, accepted en bloc, and his terms will be defined below. Sollas (1453) has used a number of terms in his preliminary report which I do not under- stand and which presumably nobody else understands either. It is, therefore, much to be regretted that the greater part of them are unexplained. In consequence of this I will, for the present, abstain from attempting to compile a nomenclature of Tetraxonid spicules pending the publication of Sollas’s full report, in which, we may hope, he will explain his new terms. The spicules of Sponges are, as a rule, of such shape that they appear as more or less modified geometrical figures with definite axes. The axes are always represented by a non-skeletal rod (the so-called axial canal), round which the silica or lime is precipitated in con- centric layers. There may be one such axis, or there may be more than one. Hickel (627) drew attention to this crystalline regularity of sponge-spicules, which has been of great importance in studying the skeletal elements of Sponges. We can divide the sponge-spicules, as we do the Sponges, into the two groups Calcarea and Silicea, according to their chemical composition, Within each group we distinguish series of forms according to the number and position of the axes. ‘The validity of this classification is proved by the correlation of these different kinds of spicules with other organs in the Sponges. The following are the different kinds of spicules :— I. Group Sprcuta CaLcaRrEa. Composed chiefly of carbonate of lime. 1. Monaxonia. With one straight or curved axis, rod-shaped. 2. Triazxonia. With three distinct axes which may lie in one plane or not. When one of the rays of this tri-act spicule becomes rudimentary, Diaxonia can theoretically be produced. It is, however, advantageous to consider the Diaxon spicules as part of the Triaxonia. The calcareous triaxon spicules have only three rays—triact. 3. Tetravonia. With four axes and four rays—tetract. The points form the corners of a triangular pyramid. Generally three axes, or rays, are equivalent (tangential), and one (radial) is differentiated, longer or ° shorter than the others. II. Group Sercuna Srxicea. Composed chiefly of silica. 1. Anawonia. Without definite axes and with numerous rays—polyact. To this group belongs one kind of spicule only, namely the stellate and its derivatives. 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 561 The following six forms can be distinguished :— A. Regularia. The rays radiating from one point. 1. Oxyaster. With long, slender, pointed rays (e. g. Stelletta). = st, Vosmaer. 2. Euaster. With stout, pointed, conic rays (e. g. Chondrilla). =gl. st, Vosmaer. 3. Spheraster. The rays coalesce to form a solid ball (e.g. Geodia).=gl, Vosmaer. B. Irregularia. The centre extends to form a line which may be curved, circular, ring-shaped, or spiral. 4. Spiraster. A stout spiral with thick spines attached (e.g. Raphyrus). = sé’, Vosmaer. When spines terminal, Amphiaster. 5. Corona. A spined ring (e.g. Suberocorona) (°). 6. Spirula. A spiral without spines ia g. Spiretta). These anaxon spicules never form part of the supporting skeleton, but are invariably flesh-spicules (Microsclera). 2. Monaxonia. With one straight or curved axis, sometimes with lamellar out- growths. A. Supporting Spicules (Megasclera). 1. Strongylus. A cylindrical rod rounded at each end (e. I: Uruguaga). = tr’, Vosmaer. 2. Owystrongylus. A cylindrical rod abruptly pointed at each end (e. g. Pachychalina). 3. Oxyus. A gradually pointed, spindle-shaped spicule (e.g. Spongilla). = ac, ac, and ac’, Vosmaer. Diact, F. E. Schulze. 4. Tylotus. A cylindrical rod with a knob at each end (e. g. Crella). = tr™, Vosmaer. 5. Tylostylus. A cylindrical rod more or less pointed at one end and knobbed at the other (e. g. Suberites). = tr° ac, Vosmaer. Without knob, Stylus. Proc. Zoou. Soc.—1886, No. XXXVII. 37 562 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, B. Flesh-Spicules (Microsclera). 6. Towius. Curved in the centre, the two ends in a straight line, thus __ (e.g. Toxochalina).=f\, Vosmaer. When in bundles, 7owodragmata. 7. Sigmata. S-shaped, curved irregularly, not expanded in one plane (e. g. Gel- liodes).= ~, Vosmaer. When in bundles, Sigmadragmata. 8. Isochele. Curved spicules with flat expanded ends extending in the surface of a rotation ellipsoid ; both ends equal (e.g. Desmacidonide). =anc’, Vosmaer. Anchorates, auctorum. 9. Anisochele. Curved spicules with flat expanded ends extending in the surface of a rotation ellipsoid ; ends unequal (e. g. Desmacidonide). =anc, anc, Vosmaer, Anchorates, auctorum. 10. Diankistra. A rod with a hook at each end, divided by a remarkable incision (e. g. Vomerula).=- J Vosmaer. Bundles of hair-like spicules, Trichodragmata. 3. Triazonia. Spicules with three axes and six rays and their derivatives. (For details compare F. E. Schulze’s preliminary report.) 1. Oxyhevact. With six pointed rays, the ends of which form the corners of a double square pyramid. The rays represent the crystalline axes. 2. Owypentact. One ray rudimentary, representing the axes of a simple square pyramid. 3. Oxytetract. Two rays rudimentary, representing the edges of a square pyramid. 4. Oxydiact. Four rays rudimentary, only two rays lying in one straight line remain. 5. Hezaster. A star with six, generally equal rays :— a. Oxyhexaster. Rays pointed. b. Discohexaster. Rays terminated by disks. c. Floricome. Rays terminated by a bunch of curved branches. 4, Graphiohexaster. Rays much curved. Plumicome. ays terminated with a number of plumose branches. 6. Pinnule. A star with five or six rays. One of them is particularly highly 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 563 developed and branched or covered with disks or scales. The oppo- site ray smooth or absent. The other four equal (tangential). 7. Scopule. Fork- or broom-shaped spicules consisting of a long shaft traversed by an axial rod, to the distal end of which some, generally four, slender anaxial rods are attached. 8. Amphidise. A rod with an umbrella-shaped disk at each end. 9. Uncinate. A rod with recurved hooks throughout its entire length. 10. Clavule. A rod pointed at one end and bearing a knob or disk at the other. 4. Tetraxonia. With four axes radiating from one point. The ends of the spicules lie in the corners of a square pyramid and their derivatives. A. Tetractina. With four rays. B. Triactina. With three rays. C. Diactina. With two rays. D. Monactina. With one ray. For the reasons given above, I shall abstain from describing the Tetraxonian spicules in detail. I will, however, mention the terms for spicules employed by Sollas in his preliminary report (1453). These, alphabetically arranged, are the following :— Acerate (Monaxon). Globate (Scleraster). Acerella (Monaxon ?), Globules (?). Amphiaster (?). Hispidating Acerate (Monaxonia), Amphiastrella (Spirastrella ?). xOne-pronged (unicellate) Forks. xAmphitetrad. xPorrectate Forks. Anchors. Pyenaster (?). Anthaster (?). Radical Anchors, Arculus (?). Sigmella (?). Bifurcated Forks, #xSomal Anchor. Calthrops (?). Somatic Anchor. Candelabra. Spinispirule (Spirastrella). Chiaster (?). Spirule (Spirulz). Cylindrical spicules (Monaxonia ?). Stellate (?). Echinella (?). xTetrad. Ecta.ter (?). xTriona. Erdaster (?). Trichite Acerates (Monaxonia), *Forls. *Trichite Forks. «Forks with trifurcate arms. xTrifid Forks. *Fusiform Acerates (Monaxonia). *xTwo-pronged (dicellate) Forks, The names marked * presumedly apply to Tetraxon spicules. The others probably belong to different groups. 37* 564 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Deec. 21, These pages will give a key to the terms of spicules used below. There are, however, a number of other terms which require explanation. The spicules are divided generally into two distinct groups :— (1) Those which together form the supporting skeleton of the sponge: these are called Supporting spicules or Megasclera. (2) Those which lie scattered in the ground-substance and which differ from the former in shape: these are called Flesh-spicules or Microsclera (Tension-spicules of Bowerbank). 4 F. E. Schulze (1369) uses particular terms for spicules according to their position, which have been adopted in this paper so far as the Hexactinellids are concerned. These are alphabetically the following :— Autodermalia. Spicules on the outer surface with free projecting and with centripetal (immersed) differentiated rays. Autogastralia, Spicules on the gastral surface with free pro- jecting and with centrifugal (immersed) differentiated rays. Basalia. Spicules of the root-tuft. Comitalia. Spicules accompanying the fibres. Epidermalia. Spicules on the outer surface with free projecting differentiated ray only. Epigastralia. Spicules on the gastral surface with free projecting differentiated ray only. Hypodermalia. Spicules of the outer surface with immersed radial ray only.—Pentact. Hypogastralia. Spicules of the gastral surface with immersed radial ray only.—Pentact. Marginalia, Spicules forming a collar round the osculum. Parenchymalia. Spicules in the interior. Pleuralia. Spicules forming a fur. Principalia, Spicules of the main skeleton. Ill. Tur Systematic Posirion or SPONGEs. The opinions of different authors on this subject diverge con- siderably. I shall attempt to reconcile them in the following pages and to prove the correctness of the result at which I have arrived. Aristotle first pointed out that the Sponges were not plants—a fact which seems clear enough now, but which was doubted and combated by most authors of the dismally ignorant middle ages. This we admit as proved. I agree with Hackel in dividing the organic world into the three groups—Plants, Protista, and Animals. Among the Protista there are a great majority of forms showing affinities either to animals or to plants, so that it is not unusual to split up the Protista and divide its members among the two other old estab- lished groups. For the sake of simplicity I adopt this course here. The Animal Kingdom, in this wider sense, including the animal Protista, is naturally to be divided into Protozoa and Metazoa, of ~ 1886. ] POSITION AND CLASSIFICATION OF SPONGES, 565 which the former consist of similar and equal, undifferentiated, cells, which often remain isolated throughout life, whilst the latter pass through a unicellular stage of short duration only, and consist, when adult, of a number of different cells. There is a vast dif- ference between these two groups: the Protozoa are isocellular, whilst the Metazoa are heterocellular. The Sponges are developed in the same way as all other Metazoa and pass through the same well-known embryonic stages—the Morula, Blastula, &c. They consist, when adult, of a great number of differentiated cells. There are flat epithelial cells all over the outer surface and on the canal- wall; there are collar-cells round the ciliated chambers. There are gland-cells for different purposes, muscular and nervous cells besides ordinary tissue and ameeboid cells in the Mesoglcea or ground-substance, in which also the ova and spermatozoa are developed. It is therefore quite clear that the Sponges are not Pro- tozoa, but Metuzoa, and are, in fact, not similar to Protozoa in any way. The Metazoa are naturally divided into two Groups or Grades— the Ceelentera, with a simple undivided body-cavity, all the parts of which are in direct connection with one another; and the Ceelo- mata, which have two distinct and entirely separated body-cavities—a gastral cavity and a ccelom or perigastric cavity. The Sponges certainly have a simple and continuous body-cavity and no trace of a ccelom, so that they must be regarded as Ccelentera. Long before Hertwig established the ccelom theory, Leuckart had already perceived this important fact, and placed the Sponges among the Ceelentera accordingly. Although nobody has ever attempted to regard the Sponges as Ccelomata, there has been great opposition, principally among English authors, to Leuckart’s opinion. I dismiss the arguments of those who, like James Clark (284-294), Carter (166), and Saville Kent (772), regard the Sponges as Protozoa, on the ground that their idea of Protozoa does not harmonize with the generally adopted meaning of the term, for if it did, they could not, as logical thinkers, count the Sponges among them. Their idea of Protozoa comprises the whole Animal Kingdom, because they draw no distinction between isocellular and heterocellular organisms, and of course all Metazoa are, if this distinction be omitted, colonies of unicellular Protozoa. F. E. Schulze (1361) has taken the unnecessary trouble to refute Saville Kent’s (772) statements in detail, and to show that the latter had been guilty not only of levity in the philosophical treatment of his work, but also of recording incorrect observations. Some very excellent men, particularly Balfour (17), Biitschli (138), and Sollas (1440), are inclined to consider the Sponges as a separate group equal in value to our groups Metazoa and Protozoa. This arrangement was arrived at without regard to the division of the Metazoa into Ccelentera and Ccelomata. They contrast the sub- kingdom Porifera (Parazoa, Sollas) with the subkingdom Metazoa as a whole. With all respect to the most important opinion of Balfour, I still do not see that there is any justification for the establishment of 566 DR. Rs VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, a special Subkingdom for the Sponges. They are evidently Metazoa, and no doubt Ceelentera in the sense given above, namely the Grade Ceelentera as opposed to the Grade Ccelomata. I think therefore that the Sponges form part of the Grade Ccelentera, and I do not believe that any one will raise any objection to this statement. Now, however, we have to approach a much more difficult task, and that is, to ascertain what position the Sponges occupy within the Grade Ceelentera. In this Grade we must place, besides the Sponges, one very well- defined group of animals (the Jellyfish, Hydroids, Corals, and Cteno- phora) which is not connected with other animals by any inter- mediate form. There can be no doubt of the comparatively close affinity of all these, and the sharp distinction between them and the Sponges. In a like manner the Sponges are an exceedingly well circumscribed group, without any transitions in any direction to other animals. The Grade Ceelentera comprises, therefore, two well-defined groups :—(1) the Mesodermalia (910) or Sponges ; and (2) the Epithelaria (910) or Nematopbora (Lankester), Cnidaria (Claus), Telifera (Marshall), as they are variously termed. A. In the Mesodermalia the archenteron communicates with the outer water by numerous small pores through which the water- current enters; and by one or a few larger pores termed oscula or vents, through which the water is expelled. It consists here of a branching canal-system. In the Epithelaria there is no branching canal-system. The anus and mouth are not distinguished, and the mouth or mouths are equivalent to all the openings of the canal-system of sponges. Only exceptionally two different kinds of pores are met with, as in certain Actiniz with terminally open tentacles; but there is no regular current of water through these pores. _ B. The gastrula of the Mesodermalia is generally produced by invagination. The gastrula of the Epithelaria, on the other hand, is generally the result of delamination. C. The Mesodermalia have no movable appendages wherewith to catch their prey. The Epithelaria have such appendages. D. The Mesodermalia are not armed with cnidoblasts or their homologues. The Epithelaria are defended by cnidoblasts or their homologues. Although these differences are important, yet the principal dis- tinction between these two groups, to which I drew attention at the Me meeting of the British Association (Meeting 1886), is the fol- owing :-— E. The Mesodermalia have invariably simple ectodermal and entodermal epithelia, the cells of which are always flat pavement- cells, and never converted into muscular, glandular, sexual, or sensi- tive elements. The muscular, connective, slime-producing glandular, skeleton-producing glandular, sexual, sensitive, ganglionic and amee- 1886. ] POSITION AND CLASSIFICATION OF SPONGES, 567 boid cells met with in the Sponges are invariably modified cells of the mesogleea. This is particularly striking and important in the case of the muscular and sensitive elements. The Epithelaria, on the other hand, have a mesoglea the cells of which remain more or less amceboid and are not differentiated to any extent. The muscular, glandular, sexual, sensitive, ganglionic and defensive nettle-cells are produced in the epithelia, they sink below the outer cell-layer with advancing development and lie on the sur- face of the mesoglcea or supporting lamella. By a process of folding and subsequent coalescing of the fold- margins, bundles of muscular cells may become immersed in the mesogloea, and so form a mesodermal structure, which, however, must be considered a secondary mesoderm, as compared to the primary mesoderm represented by the mesogloea and its cells. But they are invariably produced first from the epithelia and immersed afterwards, and always retain their epithelial character in clothing the walls of tubular cavities in the mesoglcea. Single muscular cells are never surrounded on all sides by the mesoglcea. Solid bundles of muscular cells do not occur. Exceptionally nettle-cells (Cram- bessa) may be found in the mesoglcea, which is also here and there traversed by nerve-fibres (Cycloneurous Meduse). From a common sac-shaped ancestral form with simple ectoderm, simple entoderm, and undifferentiated cells in the intervening meso- gloea, representing the type of the Ccelentera, both Mesodermalia and Epithelaria have been developed. In the case of the Mesodermalia the cells of the mesogloea became differentiated, and produced the organs, whilst the epithelia remained simple. In the case of the Epithelaria the cells of the mesogloea remained unchanged and the organs were produced by the epithelia. I regard this as the principal difference dividing the two groups, and have therefore established the term Epithelaria in contradistinction to Mesoder- malia (J. c.). Having thus described the points of distinction, it remains that we should ascertain their phylogenetic value. There are only two alternatives with regard to the value we may attach to the Sponges as.a group. Either we must assume that within the Grade Ccelentera the Phylum Mesodermalia and the Phylum Epithelaria should be distin- guished ; or we may say that there is only one phylunin the Grade Ceelentera, namely the Phylum Ccelentera, and that this should be divided into the two Subphyla Mesodermalia and Epithelaria. It is evident that it comes much to the same thing. In this matter I adopt F. E. Schulze’s opinion (1369), and consider the Sponges a separate phylum. The result of this critical examination is given in the accompanying tabular view. If we express this arrangement in the usual manner, we have :-— DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 568 ‘VHOHAONTLD SS¥IQ “G "WSAAUNOHAXOY S8UIQ) “F ‘VIUVINILOY 8SefO ‘g ‘WSNCINOUGATY SSV[Q *Z "WIONOdG S8U[Q | | | ‘stig AJUD *plosn poy ‘prodAjog ‘ssvtQ ATU ‘ssviQ A[UO Cg ee a | *DIONIVYT SLY ‘Dyjoonydy Seley *T ‘agyjaoeyd UIEAL ‘e[poowgd quoyyt A ‘yuoHdoNaLD dnory °z ‘wshdaWwodATog dnowy *T *SJ8U[qoprue ynoy}IA pue smo.t-oyppud yr AQ. ‘sysv[qopruo 414 prodéjog ‘VITYNudaosayy wnsyg “Tt “erpoyyidy otf} FO s[peo “ea Sosa, OY} FO S[T99 viody podoyaaop suvs19 wo pedopesop suRsIQ a “VLVINOTDO 9PBD VURINATWDD P&H T “JOUTJSIP SOT}TATO nec fee [eaqsey “Aqravo-Spoq eydunis WAI AA VOZOLOUd Wopsuryqng ‘T FOV Te0010}0 77 “ae [N][A00sy ries SPECS aaeh YT iy soe "VITVIAINY ™opsuryy ‘VINVIGHLIagy wnysgg -Z 1886. ] POSITION AND CLASSIFICATION OF SPONGES, 569 Kingdom ANIMALIA. I. Subkingdom PROTOZOA. Animals which are either unicellular, or, if multicellular, isocellular, without archenteron. II, Subkingdom METAZOA. Multicellular, heterocellular animals with archenteron. I. Grade CHXLENTERA. Metazoa with simple body-cavity. i. Phylum MesopERMALIA. Ceelentera with branching canal-system, and organs developed from cells of the mesoglcea or primary mesoderm. No movable appendages. 1. Class SPONGIA. With the characters of the phylum. i. Phylum EprrHEvARIA. Ceelentera with czecal canal-system. The organs are developed from cells of the epithelia. With movable appendages. 1. Group PotyromeEpus2&. Polypoid Epithelaria with cnidoblasts. i. Series Aphacelle. Polypomedusze without entodermal phacellee. 2. Class HYDROMEDUSA. Aphacelle of polypoid and medusoid character. Meduse eycloneur, ii. Series Phacellote. Polypomedusze with entodermal phacelle. 3. Class ACTINIARIA. Polypoid Phacellotz with funnel and septa. 4, Class SCYPHOMEDUSA. Medusoid Phacellote developed direct or from a Scyphostoma by strobilation. Toponeur, II. Group Crenornora. Epithelaria with paddle-rows without enidoblasts. Centroneur. 5. Class CTENOPHORA. With the characters of the group. II. Grade COAALOMATA. Metazoa with distinct gastral and ccelomic cavities. 570 DR. R. VON LENDENFELD ON THE sysTEMATIC [Dec. 21, IV. Tue CLASSIFICATION OF SPONGES. Having thus ascertained the systematic position of the Sponges as a group, we now approach the second part of our work. Every one will agree that no satisfactory classificatory system of Sponges exists at present. Spongologists are in the habit of approach- ing this subject with great caution, I may say with diffidence. It is a remarkable fact that the leading spongologist of the day, my esteemed teacher Prof. F. E. Schulze, in Berlin, has not attempted to work out a classificatory system of Sponges, whilst others have made some desultory efforts in that direction. It is self-evident that the systems established by Bowerbank, O. Schmidt, Gray, and others, which date from a time when virtually nothing was known . about Sponges, have now become obsolete. The most successful attempt at establishing a system of Sponges is doubtless that of Vosmaer (1550), who, however, approaches his task with great diffidence ; everywhere we meet in his work with ‘ preliminary ” classifications. Some geologists, principally Zittel (1635) and Sollas (1455), have classified the Sponges in a rather high-handed manner, establishing subclasses, orders, &c., without regard to details like families and genera. Zittel particularly attached too much importance to the fossil Sponges. In the groups themselves more satisfactory detail work has recently been done. F. E. Schulze (1369) has worked out the Hexactinellids of the ‘ Challenger’ with results which are as valuable and useful as the material at his disposal was abundant and interesting. Zittel (1626-1629) has in a satisfactory manner dealt witb the fossil Sponges belonging to the same group. The Lithistids and Tetractinel- lids, both fossil and recent, have been carefully investigated by Zittel (1639) and Sollas (1453). 1 (888) have, with the aid of the works of Hackel (627-629) and Poléjaeff (1179) at my disposal, established a system of Calcareous Sponges based on my investigations of the rich Australian Sponge-fauna, which appears fairly satisfactory. The Monactinellids have been carefully studied by Vosmaer (1545), Ridley (1261), and Ridley and Dendy (1265-1266), and I have myself devoted much labour to their investigation, and have made (870) an attempt at classifying them, which, however, was unsuc- cessful. The Australian Fauna is exceedingly rich in Monactinellids, and my collection, of over 300 species, has enabled me to work out the classification of some of the groups in detail. No attempt has hitherto been made to classify the Horny Sponges excepting one, contained in a short paper of Vosmaer (1552), establishing five groups, in accordance with the views previously expressed by myself (868), and based on the result of the researches into the structure of horny sponges by F. E. Schulze (1345, 1348, 1349, 1351) and myself (868). The Australian marine fauna is ex- ceedingly rich in horny sponges, so that I have been enabled to work out their relationsbips in detail. If we review the Sponges as a whole, we shall be struck with the great fundamental difference between the Calcareous and all 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 571 the other Sponges. Grant (526) was the first to point this out, and he accordingly divided the Sponges into Calcarea and Non- Calearea. Vosmaer (1550) agrees in this point with Grant and uses his terms. I have also (888) adopted the same view. In this paper I intend to alter the term Non-Calearea, which is misleading, inasmuch as it might be interpreted as meaning that the group so named consisted of very heterogeneous elements, coinciding with each other only in one, and that a negative character. This is not the case. I divide the Classis Spongize accordingly into two Subclasses, I. Cal- carea, and ITI. Silicea. The point of distinction between these two Subclasses is, that all the Calcarea have a skeleton composed of spicules consisting chiefly of carbonate of lime. All the other Sponges, which I comprise under the heading Silicea, either have a skeleton composed of sili- ceous spicules or have been derived phylogenetically from siliceous Sponges, and have only recently lost their spicules or replaced them with a horny support. O. Schmidt (1305) and also myself (870) were inclined to think that some of the siliceous Sponges had descended from horny ones. I have, howey er, since abandoned this view (901), and consider that the opposite direction of develop- ment, which Vosmaer (1558) advocates, is the correct one. We have accordingly :— Classis SPONGLAS. Skeleton composed chiefly of Skeleton originally composed carbonate of lime. of siliceous spicules. I. Subclassis CaucarEa. II. Subclassis Srzicea. As mentioned above, in the critical introduction to this chapter, I have nothing to add to my system of Calcareous Sponges (888) published some time ago, and I adopt it unchanged in this paper. The Calcarea are a very much smaller group than the Silicea. In this Subclass we only distinguish one Order, the Calcispongiz (Blainville); whilst the Silicea must be divided into several Orders, and it is here that we meet with the greatest difficulty in ascertaining the true relationship of the different forms. There are no transitions between the two subclasses. In examining the structure of a great number of Sponges belonging to this second group, the subclass Silicea, I found that they can be arranged in three Groups, which will appear as Orders in my system. These are the Hexactinellida, the Chondrospongi, and the Cornacuspongiz. These groups are fairly distinct, and transitional forms connecting them are rare. The Sponges of these Orders are descended from siliceous Sponges, and show the same tendency of development within each group. In the Hexactinellida we invariably meet with a skeleton composed of triaxial spicules; these are often attached to each other by a siliceous cement which greatly strengthens the structure. All authors agree that the Hexactinellida form a well-defined group. The remaining Silicea, however, are a very mixed lot, and before Vosmaer, no satisfactory arrangement of them had been arrived 572 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Deec. 21, at. The one I propose in this paper, which is similar to that of Vosmaer, is certainly very far from being as perfect as I would like to make it; but I think that at all events it is much more likely to express the relationship of Sponges in a correct manner than any other existing arrangement. The subclass Silicea minus the order Hexactinellida comprises the Sponges with a skeleton composed of tetraxial spicules (the Tetrac- tinellida and Lithistide of Marshall and other authors), the Sponges with monaxial spicules (the Monactinellida of Zittel and other authors), the Sponges with a horny skeleton and without spicules in the supporting skeleton (the Ceraospongiz or Keratosa of many authors), and, finally, the Sponges without any supporting skeleton at all (the Myxospongize of Hiickel). At first sight all these forms appear connected with each other in every direction by transitional forms to such an extent that it seems hopeless to bring order into this chaotic mass. A careful investi- gation of many forms shows that all the familiar groups Tetracti- nellida, Lithistidse, Monactinellida, Ceraospongiee, and Myxospongiz run into each other at every point. If one, however, for years endeavours to find some constancy in the varying characters of any chaotic mass of this kind, he at last generally arrives at an idea which seems clear enough when once grasped. And then one only wonders how it was that it had not been conceived a long time ago. So it was also in this case. I found that all these Sponges could be very naturally divided into ¢wo Orders—the above-mentioned Chondro- spongie and Cornacuspongie, the first of which comprises the Lithistids, Tetractinellida, and portions of the Monactinellida, together with most Myxospongie ; whilst the second contains all the Cerao- spongiz, and the remainder of the Monactinellids and Myxo- spongiz. We find that the ground-substance, the mesodermal intercellular substance or Mesogleea, as it is variously termed, is more or less hard and cartilage-like in the Chondrospongiz, and that in these the spi- cules remain isolated. The spicules are either tetraxon or tylostyles, less frequently styles. The monaxon spicules are monact, thereby indicating their closer affinity with the tetraxon spicules. The necessary toughness is given to these Sponges not by a cementing of the spicules, but by a hardening of the ground-substance. In some the spicules disappear altogether, as in Oscarella, which is an aske- letous form of Plakina, and in Chondrosia, which is an askeletous sponge belonging to the Tethya group. In the Cornacuspongiz, on tbe other hand, there is no tendency towards a hardening of the ground-substance discernible. The ground-substance remains soft and gelatinous, and the necessary toughness is given to the sponge by the formation of a substance not found in other Sponges, which cements the spicules together. This substance is chemically and physically comparable to silk or horn, and is known as Spongin. The spongin may become very voluminous and the spicules scarce and small. ‘They may finally disappear altogether, and then 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 573 we have Ceraospongiz before us. Transitional forms between the Cornacuspongie with supporting spicules cemented by spongin, and Cornacuspongiz without spicules in their fibres (horny sponges), are not unfrequent. One whole subfamily, the Chalininee, comprising nearly 300 species, is composed of such transitional forms. The supporting spicules met with in the Cornacuspongiz are invariably monaxon without a swelling at one end. Besides these more or less rod-shaped sup- porting spicules, we also find in some of the Sponges belonging to this group so-called flesh-spicules—small, irregular curved or complicated elements scattered throughout the Mesoglcea. These occur associated with spicules in the fibrous supporting skeleton and also in those forms which have no spicules in their horny supporting skeleton. To this group also the genera Halisarca and Bayalus belong, which have no skeleton at all, and appear as askeletous forms of the Aplysillide type. The term Cornacuspongize was established by Vosmaer (1550), and used by him in a very similar sense to that in which it is used here. The group Chondrospongie, on the other hand, is in the sense given above a new one; it nearly coincides with Vosmaer’s group Spiculispongiz (1550). In a former paper (889) I had retained the group Myxospongiee, for the sake of convenience, preliminarily only, and agreeing at the time with Sollas (1440) that it was unnatural. The manner in which I have distri- buted the members of the Myxospongiz among other groups is in accordance with the view expressed by F. E. Schulze in a letter. We have accordingly to divide the subclass Silicea into three groups in the following manner :— Subclassis SIZICHA, Lendenfeld. Mesoglcea soft ; support- Mesogleea hard ; tough- Mesoglcea soft ; support- ingskeleton oftenstrength- | nessachieved by the hard- | ing skeleton strengthened ened withsiliceouscement. | ening of the ground-sub- | by spongin cement; or Spicules triaxon. stance. Spicules tetraxon, | exclusively formed of monaxon, anaxon, or ab- spongin, with or without sent; generally corticate. | foreign bodies. Spicules monaxon, or absent. 2. Ordo HEXACTI- 3. Ordo CHONDRO- 4, Ordo CORNACU- NELLIDA, SPONGLA, SPONGLE, O. Schmidt. Lendenfeld. V osmaer. Expressed in the usual manner, the class Spongize would be accordingly divided into four Orders in the following manner :— Classis SPONGIZ, auctorum. Ceelentera with branching canal-system, without movable appen- dages ; the organs of which are developed from cells of the mesoglea. With simple epithelia. I. Subclassis CALCAREA, Grant. Spongiz with a skeleton composed of spicules which consist chiefly of carbonate of lime. 074 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dee. 21, 1. Ordo CALCISPONGIA, Blainville. The oaly Order, with the characters of the Subclassis. II. Subclassis S7ZJCEA, Lendenfeld. Spongiz with a skeleton composed of siliceous spicules and their descendants with horny aspiculous skeleton and askeletous forms. 2. Ordo HEXACTINELLIDA, O. Schmidt. Silicea with soft mesogloea. Supporting skeleton often strengthened with siliceous cement. Spicules triaxon. 3. Ordo CHONDROSPONGIA, Lendenfeld. Silicea in which the toughness is achieved by the mesoglea or mesodermal ground-substance becoming cartilaginous, whilst the spicules remain isolated. Spicules tetraxon, monaxon (tylostylus), or absent ; generally corticate. 4. Ordo CORNACUSPONGIA, Vosmaer. Silicea with soft mesoglcea or mesodermal ground-substance; the supporting skeleton, composed of bundles of monaxonid not tylostyle spicules, is strengthened by spongin, which cements the spicules. These may disappear altogether, and the skeleton is then composed of spongin with or without foreign bodies. The skeleton rarely dis- appears altogether. Having thus divided the Class Spongize into four Orders, we may preceed to the further division of the Orders into Families. I. Ordo CALCISPONGIA, Blainville. This Order has been divided by Hickel (627-629) into the well- known three families Ascones, Leucones, and Sycones, with seven genera in each. Poléjaeff (1179) has divided the group into two Suborders and replaced Hickel’s genera by the older and wider genera of Grant and others. I (888) have tried to combine Hiickel’s and Poléjaeff’s classifications, and have added three new families to the existing ones. I have retained Poléjaeff’s terms for the two Suborders, but have altered their meaning. In some Calcareous Sponges the whole of the entoderm consists of collar-cells. There are no entodermal pavement-cells in these forms. These constitute my first Suborder Homoceela. In others the collar-cells are found in the ciliated chambers only, while the central gastral cavity is clothed with entodermal pavement-cells. I combine these forms in the Suborder Heteroceela. To the Homoceela belong besides Hiackel’s Asconidz, my families Homodermide and Leucopside. I acknowledge Hickel’s seven genera of the Asconide. In the Heteroceela, Hickel’s families Leuconide and Syconidz seep with Carter’s Teichonidee and my family Sylleibide are placed. 1886.] POSITION AND CLASSIFICATION OF SPONGES. 579 II. Ordo HEXACTINELLIDA, O. Schmidt. Schulze (1369) divides the living Hexactinellida into the two Suborders Lyssacina and Dictyonina of Zittel. In the first, the spicules remain isolated or coalesce secondarily in an irregular manner ; in the second, the main spicules coalesce to begin with in a very regular manner, so as to form a continuous scaffolding. In the first suborder Lyssacina, the families Euplectellide, Gray, Asconematide, F. E. Schulze, Rossellide, F. E. Schulze, and Hyalonematidee, Gray, are placed. The second suborder, Dictyonina, comprises the families Farreide, Gray, Euretide, F. E. Schulze, Melittionide, Zittel, Coscinoporide, Zittel, and Meandrospongide, Zittel. To these the fossil families Ventriculitidee, Staurodermide, Callodictyonidze, Cceloptychide, Receptaculitide, and Monakidee must be added. In the classificatory scheme below, Schulze’s diagnoses are translated. III. Ordo CHONDROSPONGLA, Lendenfeld. As mentioned above, this Order coincides nearly with Vosmaer’s (1550) order Spiculispongie. I divide it into the two groups, Tetraxonia and Monaxonia. The former comprises the Sponges with tetraxon spicules, Tetractinellids and Lithistids ; and the latter those forms which haye monaxon spicules, or which have no spicules at all. Sollas (1453) divides the Tetraxonia into two groups :—Choristida, Sollas, without lithistid sclerites; and Lithistida, Zittel, with lithistid sclerites. In the first group the families Plakinide, Pachastrellide, Corticide, Tetillidee, Theneide, Stellettidee, and Geodine are distinguished. Vosmaer (1550) divides the Lithistidse, in accordance with Zittel (1639) and O. Schmidt (1306, 1322), into the families Rhizomori- nidew, Megamorinide, Anomacladinide, Tetracladinide. The Monaxonia comprise the families Suberitide, Spirastrellidee, Tethyde, and Chondroside. The Clavulina and portion of the Oligosilicina of Vosmaer. IV. Ordo CORNACUSPONGLE. I divide the Cornacuspongiz into the two suborders Halichondrina with, and Ceraospongize without, proper spicules in the supporting skeleton. The Halichondrina comprise the three families Homorhaphide, Heterorhaphide, and Desmacidonide of Ridley and Dendy (1265, 1266). The Ceraospongie are divided by me into two groups—Macro- camerze with large, and Microcamere with small, ciliated chambers. To the former belong the families Aplysillidee and Spongelide, and to the latter the Spongidee, Aplysinide, and Hircinide. After this general view of the Classification of Sponges, I shall proceed to give a “system”? of Sponges down to subfamilies, mentioning the principal genera in each group. 576 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, Classis SPONGIAS, auctorum. Ccelenterata with branching canal-system, the organs of which are developed from cells of the mesoglcea or primary mesoderm. With simple epithelia, with entodermal collar-cells, and without movable appendages and enidoblasts. I. Subclassis CALCAREA, Grant. Sponges with a skeleton composed of calcareous spicules. I. Ordo CALCISPONGILA, Blainville. The only order, with the characters of the subclass. 1. Subordo Homoca@ a, Poldjaeff, emend. The entodermal epithelium consists exclusively of collar-cells. 1. Familia Asconip#, Hickel. Simple sac-shaped gastral cavity with smooth surface. Leucosolenia, Poléjaeff, Ascetta, Ascissa, Ascilla, Ascaltis, Ascor- tis, Asculmis, Ascandra, Hackel. 2. Familia HomopERMID#, Lendenfeld. The gastral cavity forms cecal outgrowths, which resemble the tubes of Syconidee. Ascaltis canariensis, Hiickel, Ascaltis lamarckii, Hickel, and Homoderma sycandra, Lendenfeld. 3. Familia LEucorsip#, Lendenfeld. A colony of Ascon-persons which are imbedded in the thick mesogloea. There are narrow inhalant pores and wider exhalant ones. The latter lead into a pseudogaster. Leucopsis, Lendenfeld, and some species of Psewdonardorus-forms 11. Subordo HeTEROCGLA, Poléjaeff, emend. The entodermal epithelium is differentiated into collar-cells, which are found in the walls of the ciliated chambers only, and into flat pavement-cells, which clothe the walls of the exkalaut canals and gastral cavity. 4. Familia Syconip&, Hiickel. With regular, radially disposed cylindrical ciliated chambers, which open direct into the sac-shaped gastral cavity. 1. Subfamilia Syconine, Lendenfeld. The unbranched ciliated chambers remain isolated in their distal part. Sycon, Poléjaeff, the subgenera of Hickel’s Syconide which ter- minate with the syllable ‘‘aga.” I divide this subfamily according to Hickel’s scheme into the seven genera Sycetta, Sycissa, Sycilla, Sycaltis, Sycortis, Syculmis, and Sycandra. 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 577 2. Subfamilia Uteine, Lendenfeld. With simple unbranched ciliated chambers, the distal’ends of which are imbedded in a continuous cortex. Grantessu, Lendenfeld, Ute, Poléjaeff, and Amphoriscus, Poléjaeff, and those subgenera of the Syconide in Hiackel’s system which terminate with the syllable “usa.” 3. Subfamilia Granting, Lendenfeld. With branched ciliated chambers. Grantia, Heteropegma, and Anamiwilla, Poléjaeff. 5. Familia SyLLErBip#, Lendenfeld. With complicated exhalant canals, leading from the cylindrical ciliated chambers into the gastral cavity. 1. Subfamilia Vosmaerine, Lendenfeld. The ciliated chambers are radially situated, and form a regularly cylindrical zone. They are connected with the gastral cavity by a network of anastomosing exhalant canals. Vosmaeria, Lendenfeld, and Leucetta, Poléjaeff. 2. Subfamilia Polejne, Lendenfeld. The ciliated chambers form a much-folded layer. The exhalant canals are wide, and do not anastomose to form a reticulation. The genera Polejna, Lendenfeld, and Leucilla, Poléjaeff, consti- tute this group. 6. Familia Leuconip#, Hiickel. Heteroccela with ramified canal-system and spherical ciliated chambers. Leucetta, Leucissa, Leucaltis, Leucortis, Leuculmis, and Leu- candra, Hickel, Leuconia, auctorum, and Leuconia and Pericharaz, Poléjaeff. 7. Familia TercHonip2, Carter. Heterocceela without gastral cavity. The inhalant pores are situated on the one, and the exhalant on the other side of the lamellar sponge ; with spherical ciliated chambers. Teichonella, Carter, and Hilhardia, Poléjaeff. II. Subclassis SIZICEA, nov. Sponges with a skeleton composed of siliceous spicules and their derivatives ; possessing a horny skeleton or no skeleton at all, but never supported by calcareous spicules. Comprises the Non-Calcarea of Grant and other authors. 1. Ordo HEXACTINELLIDA, O. Schmidt. Silicea with triaxon spicules and soft mesoglea. Strengthened by siliceous cement, generally joining the spicules. Proc. Zoou. Soc.—1886, No. XXXVIII. 38 578 DR. R. VON LENDENFELD ON THE SysTEMATIC [Dec. 21 1. Subordo Lyssacina, Zittel. The spicules remain isolated or are subsequently cemented together irregularly. i. Tribus Hewasterophora, F. E. Schulze. Hexaster always found in the mesogloea; chambers distinct, thimble-shaped. 1. Familia EUPLECTELLID#, F. E. Schulze. Thin-walled tubes or sacs with sword-shaped hexact hypodermalia, the centripetal rays of which are the longest. 1. Subfamilia Huplectelline, F. E. Schulze. Tubular, with terminal sieve-plates. The wall regularly perfo- rated. To the centrifugal ray of each hypodermal a floricome is attached. Euplectella, Owen, and Regadrella, O. Schmidt. 2. Subfamilia Holascine, F. E. Schulze. Tubular, wall without perforations, without superficial flori- comes. Holascus and Malacosaccus of F. E, Schulze. 3. Subfamilia Taegerine, F. EK. Schulze. Tubular or sac-shaped, wall irregularly perforated. Principalia partially cemented, forming an irregular network. To the distal ray of each hypodermal sword-shaped hexact a floricome is attached. Taegeria and Walteria of F, E. Schulze. 2. Familia AScoNnEMATID#, F. E. Schulze. Pentact or hexact pinnule in the dermal and gastral surfaces. Hypodermalia and hypogastralia pentact. Discohexaster in the interior. 1. Subfamilia Asconematine, F. E. Schulze. Sessile, sac-shaped, or tubular, with thin soft wall. Asconema, Say. Kent, and Aulascus, F. E. Schulze. 2. Subfamilia Sympagelline, O. Schmidt. Pedunculate, cup-shaped. Principalia hexact and diact. Disco- hexaster in the interior. Sympagella, O. Schmidt, Polyrhabdus, F. E. Schulze, and Bala- nites, F. E. Schulze. 3. Subfamilia Caulophacine, F. E. Schulze. Mushroom-shaped, with long cylindrical hollow peduncle. Caulophacus and Trachycaulus of F. KE. Schulze. 1886. | POSITION AND CLASSIFICATION OF SPONGES. 579 3. Familia Rossetuips, F. E. Schulze. The dermalia have no centripetal ray. Lanuginella, O. Schmidt ; Polylophus, F. E. Schulze ; Rossella, Carter ; Acanthascus, Bathydorus, Rhabdocalyptus, Crateromorpha, Aulochone, Caulocalyx, and Aulocalyx, F. E. Schulze. ii. Tribus Amphidiscophora, F, E. Schulze. Amphidiscs in the limiting membranes. Hexaster absent in the interior. A basal tuft is always present. The ciliated chambers appear as somewhat irregular sac-shaped extensions of the membrana reticularis. 4, Familia HyALONEMATIDA, Gray. Numerous pentact pinnule in the dermal and gastral surfaces. 1. Subfamilia Hyalonematine, F. E. Schulze. Calyculate, with a well defined oscula-area on the upper surface. Hyalonema, Gray ; Stylocalyz, F. E. Schulze; Pheronema, Leidy ; and Poliopogon, Wyville Thomson. 2. Subfamilia Semperelline, F. E. Schulze. Without gastral cavity and terminal oscula-area, with root-tuft. Semperella, Gray. To this Subordo the fossil families Receptaculitidee and Monakidee belong. u. Subordo Dictyonina, Zittel. The parenchymal hexacts early coalesce in a regular manner, so as to form a firm skeleton. i. Tribus Uncinataria, F. E. Schulze. With uncinates. i. Subtribus Clavularia, F. E. Schulze. With radially situated clavule. 1. Familia Farreipa#, F. E. Schulze. The skeleton forms a single layer; from the joining points conical extensions arise, in a direction vertical to the surface of the network. Farrea, Bowerbank. 2. Subtribus Scopularia, F. E. Schulze. With radially situated scopulz. 2. Familia Euretipa, F. E. Schulze. Branched and anastomosing tubes. The skeleton-net forms several layers. Eurete, Carter ; Periphragella, Marshall; and Lefroyella, Wyville Thomson. 38* 580 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 3. Familia MEeLiTTIONnIp#, Zittel. Forms branched tubes or calyculate structures. Skeleton honey- combed. Cavities traversed by the reticular membrane. The gastral skeleton without scopulz. Aphrocallistes, Gray. 4. Familia Coscinoporip&, Zittel. The wall of the calyculate or expanded sponge is traversed by funnel-shaped straight canals, which open alternately on the one or the other surface. Covered only by the perforated limiting mem- brane. Chonelasma, F. E. Schulze ; and the fossil genera Leptophragma, Zittel, Guettardia, Michelin, and Coscinopora, Goldfuss. 5. Familia Treropictyipa&, F. E. Schulze. With irregular inhalant and exhalant canals, which do not traverse the body transversely, but pass the dense dictyonal skeleton obliquely or longitudinally. Tretodictyum, F. E. Schulze; Euriplegma, F. E. Schulze ; Cyr- taulon, F. E. Schulze; Fieldingia, Sav. Kent; and Sclerathamnus, Marshall. ii. Tribus Inermia, F. E. Schulze. Without uncinates and scopulz. 6. Familia MranpRosPoncGip4, Zittel. The body consists of winding tubes of uniform width. The in- terstices of the tubes form a vestibule space. Dactylocalyx, Stutchbury ; Scleroplegma, O. Schmidt ; Margari- tella, O. Schmidt ; Myliusia, Gray ; and Aulocystis, F. E. Schulze ; and the fossil genera :—Placoscyphia, Reuss; Tremabolites, Zittel ; Etheridgia, Tate; Cystispongia, Roemer; Toulminia, Zittel; and Camerospongia, d’Orb. To this Subordo belong the fossil families Ventriculitide, Stauro- dermidz, Callodictyonidee, and Cceloptychide. II. Ordo CHONDROSPONGIA, nov. Silicea in which the toughness is caused by the mesogloea or mesodermal ground-substance becoming cartilaginous, whilst the spicules remain isolated. Spicules tetraxon, monaxon (tylostylus or stylus), or absent. With spherical ciliated chambers. Sponge gene- rally corticate. Comprises the Spiculispongiz of Vosmaer, with the exception of the genus Halisarca, Vosmaer. 1. Subordo TeTRAxXONIA, Vosmaer. With tetraxon spicules. 1886.] POSITION AND CLASSIFICATION OF SPONGES, 581 1. Group Liraistrpa, Zittel. Body stony, with a central gastral cavity or numerous vertical tubes. Spicules more or less clearly tetraxon, often branched. Besides these, sometimes monaxon spicules and flesh-spicules. The skeleton-spicules are interwoven so as to form a dense skeleton. 1. Familia Ru1zoMoRINID«&, Zittel. Spicules irregularly branched ; form irregular fibres, or are loosely interwoven. Forked anchors always present. Arabescula, Carter; Corallistes, Schmidt ; Heterophymia, Pomel ; Seliscothon, Zittel ; MacAndrewia, Gray ; Azorica, Carter; Leioder- matium, Schmidt ; and the fossil genera :—Cnemidiastrum, Coral- lidium, Hyalotragos, Pyrgochonia, Discostroma, Leiodorella, Episto- mella, Platychonia, Bolidium, Astrobolia, and Chonella of Zittel; Plococonia, Pomel ; Chenendopora, Lamouroux ; Verruculina, Zittel ; Amphithelion, Zittel; Stychophyma, Pomel; Allomera, Pomel ; Pleuromera, Pomel; Perimera, Pomel; Meta, Pomel; WMarisca, Pomel ; Pomelia, Zittel; Jereica, Zittel ; Calocorypha, Zittel; Scy- talia, Zittel; Stachyspongia, Zittel; Pachinion, Zittel. © 2. Familia ANOMOCLADINID, Zittel. Spicules rod-shaped with terminal tufts of branches. The approxi- mating ends of the spicules coalesce and form knots. In this way a regular triaxial network is formed. Vetulina, Schmidt; and the fossil genera Mastosia, Cylindrophyma, Melonella, and Protachilleum, Zittel, and Paleomanon and Astylo- spongia, Roemer. 3. Familia TETRACLADINIDA, Zittel. Spicules tetractinellid with terminal branches. Theonella, Gray ; Rhacodiscula, Zittel ; Discodermia, Bocage ; Ka- liapsis, Bowerbank ; Collectella, Schmidt ; Collinella, Schmidt; and the fossil genera :—Aulocopium, Oswald; Phymatella, Aulaxinia, Callopegma, and Trachysycon, Zittel ; Siphonia, Parkinson; Halli- rhoa, Jerea, Lamouroux; Marginospongia, d’Orbigny ; Nelumbia, Pomel; Polyjerea, Fromentel; Astrocladia, Zittel ; Bolospongia, Hinde ; Thecosiphonia, Zittel; Calymmatina, Zittel; Turonia, Mi- chelin ; Kalpinella, Thamnospongia, and Pholidocladia, Hinde; Ra- gadinia, Zittel; Plinthosella, Zittel ; Spongodiscus, Zittel ; Phyma- plectia, Hinde; Rhopalospongia, Hinde. To this Subordo also the fossil family Megamorinidz belongs. 11. Group CHorisTIDaA, Sollas. With tetraxon spicules of regular shape. i. Tribus Tetradina, Sollas. The chief spicules are tetract, with equal rays and candelabras. i. Subtribus Microcamera, nov. With small chambers. 582 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 4. Familia Corticip, Vosmaer. With candelabras. Oorticium, Schmidt, and Thrombus, Sollas. 5. Familia PACHASTRELLID#, Sollas. With simple tetracts, irregularly scattered. Pachastrella, Schmidt, Battersbya, Bowerbank, and Dercitus, Gray. li. Subtribus Wacrocamere, nov. With large chambers. 6. Familia PLaKxinip#, F. E. Schulze. With scattered diact, triact, and tetract spicules. Plakina, Plakinastrella, and Plakortis, F. E. Schulze, and Eupalaz, Sollas. 7, Familia OscARELLIDH, Lendenfeld. Without spicules. Oscarella, Vosmaer. ii. Tribus T'rz anina, Sollas. The centres of the tetraxon spicules with one differentiated ray lie in the surface, in which the equal rays extend tangentially. 8. Familia Grop1p4, Sollas. A cortex of globate spicules. Chambers small, with small outlets. Erylus, Gray ; Caminus, Schmidt ; Cydonium, Miiller ; Synops, Vosmaer ; Isops, Sollas; Geodia, Lamarck ; and Geodissa, Lenden- feld. 9. Familia STELLETTIDs#, Sollas. With stellate flesh-spicules usually in the cortex. 1. Subfamilia Psammasterina, Sollas. With stellates and spined rods. Psammastra, Sollas. 2. Subfamilia Stryphnina, Sollas. With stellates and amphiastrellee. Stryphnus, Sollas. 3. Subfamilia Sanidasterina, Sollas. With stellate and sanidaster (?) spicules. Tribrachium, Weltner, and Tethyopsis, Stewart. 4, Subfamilia Stellettina, Sollas. With two kinds of stellate flesh-spicules. Antrastra, Dragmastra, Sollas ; Stellettc, Schmidt. 5. Subfamilia Homasterina, Sollas. With one kind of stellate flesh-spicules. Myriastra, Solias ; Asterella, Sollas; Pilochrata, Sollas. 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 583 10. Familia THEenerpas, Sollas. With large outlets to the ciliated chambers, and spirastrellid spicules. Thenea, Gray (Tisiphonia, Wyville Thomson, Dorvillia, Sav. Kent, Wyville-Thomsonia, Wright); Normania, Vulcanella, and Chara- cella, Sollas. 11. Familia TetT1Lu1p#, Sollas. With flesh-spicules which are hamate, spiral, or rod-shaped. Spiretta, Lendenfeld; Tetilla, Schmidt; Craniella, Schmidt ; Chrotella, Sollas ; Papirula, Schmidt ; Thalassomora, Lendenfeld. 12. Familia TETHYOPSILLID&, nov. Spherical sponges supported by dense masses of large radial monaxonid spicules. A few tetraxonid grapnels are inserted in the surface. Tethyopsilla, Lendenfeld, and Protoleia, Dendy and Ridley. 11. Subordo MonaxoniDa. 11. Group CLavuLina, Vosmaer, emend. With monaxonid spicules or without supporting skeleton. Supporting spicules tylostyle, usually radially situated. (Includes the Pseudotetraxonia, Vosmaer.) 1. Familia TerHyp®, Vosmaer. More or less spherical sponges, with regular subdermal cavities between the thick distally extending radial bundles of spicules. 1. Subfamilia Tethyne, nov. With stellate flesh-spicules. Tethya, Lamarck; Tuberella, Keller (Tethiophena, Schmidt) ; Tethiosphera, Lendenfeld ; Mastigophora, Lendenfeld ; T'halasso- dactylus, Lendenfeld. 2. Subfamilia Tethiopsammine, nov. With a sand cortex. Tethiopsamma, Lendenfeld, MS. 3. Subfamilia Tethyorhaphine, nov. With rod-shaped flesh-spicules, without stellates. Tethyorhaphis, Lendenfeld. 4. Subfamilia Tethyamatine, nov. With hamate flesh-spicules (sigmata) without stellates. Tethyamata, Lendenfeld, 584 DR. R. VON LENDENFELD ON THE SysTeMaTIC [Dec. 21, 2. Familia SoLLASELLID#&, Lendenfeld. Digitate forms with radiating spicule-bundles, and distinct ecto- and endochone. Sollasella, Lendenfeld. 3. Familia SprrastRELLID#, Ridley and Dendy. With spirastrellid flesh-spicules. Spirastrella, Ridley ; Raphyrus, Bowerbank ; Papillina, Schmidt; ~ Cheirella, Lendenfeld ; Awos, Gray ; and Coletrar. ona, Lendenfeld. Coincides with the family Gheirciides Lendenfeld. 4. Familia SUBERAMATIDA, nov. With hamate flesh-spicules (sigmata). Suberamata, Lendenfeld. 5. Familia SuBeRITIDZ, Vosmaer, emend. Without flesh-spicules. Suberitella, Lendenfeld ; Suberites, Nardo ; Suberopetros, Lenden- feld ; Plectodendron, Lendenfeld ; Polymastia, Bowerbank ; T'richo- stemma, M. Sars; Tentortum, Vosmaer (Thecaphora, O. Schmidt) ; Stylocordyle, Wyv. Thomson ; Quasillina, Norman; Cliona, Grant; and Poterion, Schlegel. Iv. Subordo OL1GosiLicina, Lendenfeld. Without supporting skeleton. Flesh-spicules, when present, anaxon polyactinellid. Chambers small, with narrow outlet. 1. Familia CoonpRILLID&, Lendenfeld. With polyactinellid flesh-spicules. Comprises the genus Chon- drilla, O. Schmidt. 2. Familia CoonpRosip#, Lendenfeld. Without flesh-spicules. Comprises the genus Chondrosia, Nardo. III. Ordo CORNACUSPONGIA, Vosmaer, emend. Silicea with soft mesogloea, or mesodermal ground-substance. The supporting skeleton is composed of bundles of monaxonids, which are never tylostyle spicules. The skeleton is strengthened by spongin, which cements the spicules. These may disappear altogether, and the skeleton is then composed of spongin, with or without foreign bodies. Exceptionally, also, this horny skeleton disappears. The ciliated chambers have large outlets. 1. Subordo HALICHONDRIN‘A, Vosmaer. With siliceous spicules in the supporting skeleton. 1. Familia SPonGILLIDA, Carter. Freshwater sponges with gemmule. Spongilla, Lamarck ; Ephydatia, Lamouroux; Tubella, Carter ; 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 585 Uruguaya, Carter ; Parmula, Carter ; Meyenia, Bowerbank ; Heée- romeyenia, Potts; Lubomirskya, Dybovsky; Lessepsia, Keller ; Potamolepis, Marshall. 2. Familia Homoruaruips, Ridley and Dendy. Megasclera oxea or strongyla ; no differentiated microsclera except toxia. Marine sponges without gemmule. 1. Subfamilia Renierine, auct. Spicules never completely enveloped in horny fibre. Halichondria, Fleming ; Petrosia, Vosmaer, =Schmidtia Balsamo Crivelli; Reniera, Nardo. 2. Subfamilia Chalinine, Ridley and Dendy. A considerable amount of spongin present, forming distinct horny fibres, in which spicules are contained. 1. Group Chalinorhaphine, Lendenfeld. With abundant gigantic spicules axially situated. Chalinorhaphis, Lendenfeld. 2. Group Hoplochalinine, Lendenfeld. With abundant gigantic spicules obliquely situated, and protruding beyond the fibre-surface. Hoplochalina, Lendenfeld. 3. Group Cacochalining, Lendenfeld. Irregular forms with slender spicules. Cacochalina, Schmidt; Cladochalina, Lendenfeld ; Chalinopora, Lendenfeld ; Chalinella, Lendenfeld ; Chalinopsis, Schmidt. 4. Group Pachychalinine, Lendenfeld. Irregular, digitate, lamellar forms with stout spicules, oxystron- lus. Chalinissa, Leudenfeld ; Pachychalina, Schmidt; and Ceraochalina, Lendenfeld. 5. Group Plakochalining, Lendenfeld. Frondose, lamellar forms with stout spicules. Plakochalina, Euplakella, and Antherochalina, Lendenfeld ; Cribro- chalina, Schmidt ; Tragosia, Gray ; Platychalina, Ehlers. 6. Group Siphonochalinine, Lendenfeld. Tubular, pseudogaster with stout spicules. Spinosella,Vosmaer ; Siphonochalina, Schmidt ; Tuba, Duchassaing and Michelotti; ASclerochalina, Ridley; Towxochalina, Ridley ; Phylosiphonia, Lendenfeld; Tubulodigitus, Carter; Patulascula, Carter ; and Siphonella, Lendenfeld. 7. Group Arenochalinine, Lendenfeld. With spicules in the connecting and sand in the main fibres. Arenochalina, Lendenfeld. 586 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 8. Group Zuchalinine, Lendenfeld. Slender, regularly digitate forms with a fine-meshed network and slender spicules. Chalina, auctorum, and Dactylochalina, Euchalina, Euchalinopsis, and Chalinodendron, Lendenfeld. 3. Familia HETERORHAPHID#, Ridley and Dendy. Megasclera of various forms; microsclera commonly present, but never chele. Marine sponges, without gemmule. 1. Subfamilia Phlaodictyine, Carter. Sponge divisible into body and fistule, with a strong spicular rind. Megasclera oxea or strongyla; microsclera (when present) sigmata. Rhizochalina, Schmidt ; Oceanapia, Norman. 2. Subfamilia Gelliine, Ridley and Dendy. Megasclera oxea or strongyla. Microsclera always present, viz. sigmata. No rind or fistule. Gellius, Gray ; Gelliodes, Ridley. 3. Subfamilia Tedaniine, Ridley and Dendy. Megasclera of two forms: monactinal, styli, forming the main skeleton ; and diactinal, tylota. Microsclera long, hair-like trichites. Tedania, Gray ; Trachytedania, Ridley. 4, Subfamilia Desmacelline, Ridley and Dendy. Megasclera styli to tylostyli. Microsclera sigmata or toxia, or both. Desmacella, Schmidt. 5. Subfamilia Hamacanthine, Ridley and Dendy. Megasclera oxea or styli; microsclera diankistra, to which others may be added. Hamacantha, Gray ; Vomerula, Schmidt. 4, Familia DesmMactpon1p&, Vosmaer, auct. Megasclera of various forms. Microsclera chele, to which others may be added. 1, Subfamilia Esperelline, Ridley and Dendy. Fibre not echinated by laterally projecting spicules. Esperia, Nardo; Esperella, Vosmaer ; Esperiopsis, Carter; Cla- dorhiza, Sarvs; Awoniderma, Ridley and Dendy; Chondrocladia, Wyv. Thomson; Desmacidon, Bowerbank ; Homeodictya, Artemi- sina, Vosmaer; Phelloderma, Ridley and Dendy ; Sideroderma, Ridley and Dendy ; Iophon, Gray ; Amphilectus, Vosmaer ; Melonanchora, Carter; Guitarra, Carter, 1886. | POSITION AND CLASSIFICATION OF SPONGES. 587 2. Subfamilia Ectyonine, Ridley and Dendy. Fibre echinated by laterally projecting spicules. Myzilla, Schmidt ; Clathria, Schmidt; Rhaphidophlus, Eblers ; Plumohalichondria, Carter ; Acarnus, Gray ; Echinoclathria, Carter ; Clathrissa, Lendenfeld; Thalassodendron, Lendenfeld; Cerao- spina, Lendenfeld. 5. Familia AXINELLIDs#, auct. With large subdermal cavities. Skeleton non-reticulate, consist- ing of ascending axes of fibre, from which arise subsidiary fibres radiating to the surface pervading the subdermal cavity. Fibres plumose. Megasclera chiefly styli, to which oxea and strongyla may be added. Microsclera rarely present, never chele. Dendropsis, Ridley and Dendy; Thrinacophora, Ridley; Hyme- niacidon, Bowerbank ; Phakellia, Bowerbank; Ciocalypta, Bower- bank ; Acanthella, Schmidt ; Awinella, Schmidt ; Raspailia, Nardo ; Spirophora, Lendenfeld. 11. Suborder K ERATOSA, Bowerbank, emend. Silicea with a supporting skeleton composed of spongin; fibre with or without foreign bodies, but always without proper spicules. Flesh-spicules may be present. Exceptionally, there is no skeleton at all. i. Tribus Microcamere, Lendenfeld. With small spherical ciliated chambers and opaque ground- substance. 1. Familia Sponeip2, F. E. Schulze. With narrow axial thread in the horny fibres, and without fila- ments. 1. Subfamilia Aulenine, Lendenfeld. Reticulate sponges with vestibules, without flesh-spicules. Halme, Aphroditella, Halmopsis, and Aulena, Lendenfeld ; Psam- maclema, Marshall. 2. Subfamilia Chalinopsilline, Lendenfeld. When dry of light yellow colour, digitate, lamellar, more or less flower-shaped, imitating very closely Chalinine, from which they appear only recently to have developed. Without flesh-spicules, with smooth surface. Chalinopsilla and Antheroplax, Lendenfeld ; Dactylia, Carter. 3. Subfamilia Spongine, Lendenfeld. Massive, when dry dark brown, with conulated or granulated surface. Vestibules, when present, belong’exclusively to the inhalant system. Without flesh-spicules, Euspongia, Brown ; Cacospongia, Schmidt ; Hinpospongia, F. E. 588 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, Schulze; Coscinoderma, Carter; Spongodendron, Lendenfeld; and many of the species of the genus Spongia, auctorum. 4. Subfamilia Spongissine, Lendenfeld. With flesh-spicules. Spongissa, Lendenfeld, MS. 2. Familia ApLystnip&, Lendenfeld. The skeleton is composed of spongin-tubes, the walls of which are thinner than the diameter of the lumen, which is filled with pith. 1. Subfamilia Aplysinine. Without flesh-spicules. Luffaria, Duchassaing and Michelotti; Aplysina, Nardo; Luffa- rella, Lendenfeld, MS.; Dendrospongia, Hyatt. 2. Subfamilia Aplysissine, Lendenfeld. With flesh-spicules. Aplysissa, Lendenfeld, MS. 3. Familia Hircinrp#, Lendenfeld. With narrow axial canal in the fibres, and filaments in the ground- substance. 1. Subfamilia Hircinine, Lendenfeld. Without proper spicules. Hircinia, Nardo ; Hircinopsis, Nodosina, Aphrotriche, and Sty- phlos, Lendenfeld, MS.; Stematonemia, Bowerbank ; Filifera, Lie- berkiihn ; Sarcatragus, Schmidt ; and Polytherses, Duchassaing and Michelotti. 2. Subfamilia Hircinissing, Lendenfeld. With proper spicules. 1. Group Chalinocinia, nov. With proper spicules in the conuecting fibres. Chalinocinia, Lendenfeld. 2. Group Hircinissa, nov. Without proper spicules in the fibres ; with flesh-spicules. Hircinissa, Lendenfeld, MS. ii. Tribus Macrocamere, Lendenfeld. With large sac-shaped ciliated chambers, and soft, transparent ground-substance. 4. Familia SponceLip, Lendenfeld. The horny fibres contain slender axial thread and form a reticulated skeleton. 1886.] POSITION AND CLASSIFICATION OF SPONGES. 589 1. Subfamilia Spongeline, Lendenfeld. Without flesh-spicules. The skeleton consists of distinct horny fibre containing a varying amount of foreign matter. Spongelia, Nardo; Dysidea, Johnston; and Reteplax, Lenden- feld, MS. 2. Subfamilia Psammine, nov. The skeleton consists of foreign bodies cemented by spongin, which, however, is not distinctly visible; without flesh-spicules. Psammapemma, Marshall; Psammella, Lendenfeld, MS.; and Holopsamma, Carter. 3. Subfamilia Spongelissine, Lendenfeld. The skeleton is composed of distinct horny fibres containing foreign bodies. With flesh-spicules. Dysideissa, Lendenfeld, MS. 4. Subfamilia Psammopessine, nov. The skeleton consists of cemented foreign bodies without distinct horny fibres. With flesh-spicules. Psammopessa, Lendenfeld, MS.; Phoriospongia, Marshall; and Haastia, Lendenfeld, MS. 5. Familia ApLysiLLip#,. Lendenfeld. The skeleton consists of spongin-tubes ramified in a dendritic fashion and filled with pith. 1. Subfamilia Aplysilline, Lendenfeld. Cells are found in the pith of the fibres only. Darwinella, Fritz Miller ; Aplysilla, F. E. Schulze ; Verongia, Bowerbank ; and Dendrilla, Lendenfeld. 2. Subfamilia Ianthelline, nov. Cells are found in the spongin-sheath of the fibre. Tanthella, Gray. 6. Familia Hauisarcipa, Vosmaer. Without skeleton. Halisarca, Schmidt, and Bajalus, Lendenfeld. V. Key To THe Recent FaAMI.ies OF SPONGES. 0. Skeleton calcareOus ....5.ccxccessensisexsesossessees ilF * [No calcareous skeleton .........0.000ssessceoeesseree (2.) Entoderm consists exclusively of collar-cells ... 3. 1. 4 Entoderm consists of collar- and pavement- Ae CELIA Foeaedomocnescana deve. stueaeseesmerdeeseneesca ss (4.) Mesoderm thin, gastral cavity irregular ...... 1, Ascontdae. 3. 4 Mesoderm thin, radial cylindrical chambers... 2, Homodermide. Mesoderm thick, irregular chambers ............ 3. Leucopside. 590 (4.) With cylindrical chambers *? | With spherical chambers ...........sssecosseeseeees {css radial, opening direct into gastral Fees ee ree eee eaeseneereae cavity Chambers opening into exhalant canals which lead into the gastral cavity ( Exhalants lead into oscular tubes Renee nema anew meee eee meet eee ee teen es eeeeee 5 Exhalants open direct on one side of the lamel- lar sponge; inhalant pores on the other side exclusively (6) Sete eee e tees er renters e eee eeeennene DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 2], 4. Syconide. 5, Sylleibide. 6. Leuconide. 7. Teichonide. With hexact spicules and thimble-shaped 2 Chambers J sas aeacks eke cetaueeegensencem ders tee Ue (4) Without hexact spicules, with sac-shaped or P i spherical chambers) <.....idc-senesco.es1eeceeves (8.) The spicules remain isolated or partly coalesce 7 afterwards irregularly ............coesesseeeeceee 9. * ) The supporting spicules early coalesce in a regular Dictyonid manner ..............0se006- (10.) 9 Hexaster in the interior .............sccesseeseeeee UF : | No hexasters, but amphidises ..............0.cc00- (12.) ( Hypodermalia hexact sword-shaped, with centri- 1 petal radial ray longest; no pinnule......... 8. Luplectellide. Pinnulz in the gastral and dermal surfaces... 9. Asconematide. Dermalia without centripetal ray; no pinnule 10. Rossellide. (12.) ‘With numerous pinnulee ..............02-cseeeeeees 11. Hyalonematide, 10.) Whith imneinates!;: ces cacsctascevasensvetetusteceuesaas 13. (10-) | Without uncinates ....s.s-scssssseseseserseseseeer (14.) 13 With radially situated clavule ...............04. 12. Farreide. * | With radially situated scopulee ...........-.06. 15. ( Branched and anastomosing tubes ; the skeleton- | net forms several layers ............se0esescees 13. Euretide. Branching tubular or calyculate, honeycombed ; cavities traversed by reticular membrane ... 14. Melittionide. 15. 4 Oalyculate or expanded, traversed transversely | by funnel-shaped canals opening alternately on one or other surface ...........-...s0seeeee- 15. Coscinoporide. Canals irregular, traversing the dense dictyonal | skeleton obliquely or longitudinally ......... 16. Tetrodictyide. (14.) Meandrically winding tubes ................06.6 17. Meandrospongide. With cartilaginous ground-substance and sphe- vical chambers. Spicules polyact, tetract, lithistid, tylostylote, or stylote, never ce- mented with spongin. Askeletous forms with spherical chambers .................:00000- 16. (8.) 4 With soft ground-substance, spherical or sac- shaped chambers, Spicules monaxon, never tylostylote, cemented with spongin. Or ske- leton composed of horny fibre without proper spicules. Askeletous forms with sac-shaped chambers Senter reese ee Come reece eres eererteeeneren 1886.] POSITION AND CLASSIFICATION OF SPONGES. With lithistid irregular tetraxon spicules ...... 18. (With tetraxon spicules of irregular shape ; askeletous forms with large chambers, which 16 have large outlets ............sscsecrecesseeerevees (19.) * ') With monaxon tylostylote spicules .......--.....- (20.) Without supporting spicules; flesh-spicules | when present polyact, with small chambers \ which have narrow outlets ..........ceeeeeeeee (21.) Spicules quite irregular ...........seesceseeeeerees 18. Rhizomorinide. Spicules rod-shaped, with terminal tufts of branches wee eee eee ewer e ee ee rata ee nesses eae eeeeee Spicules tetractin, with terminal branches...... 19. Anomocladinide. 20. Tetracladinide. ANd candelabras ......:c.s.cecsessoncecscssoessvers There are large tetract spicules with three equal rays lying tangentially in or beyond the surface, and one difterentiated, radial ray .. With small inconspicuous ciliated pe with small outlets With large conspicuous ciliated chambers with Wide OWGLSEA. ae ccvecbcctcscnsecncodeescenssrsevdenae With candelabra With simple tetracts (19.) bo to bo = 22. (23.) 2. (25.) . Corticide. 2. Pachastrellide. seas eeeee With scattered tetracts, triacts, diacts (25.) ) Without spicules { The spicules are chiefly tetracts with equal rays Tetracts with differentiated large centripetal ray and large tangential rays numerous ...... Tetracts with differentiated large centripetal ray rare, with small tangential rays 26 { Withispherastons'\..-55¢42sce-ccewasana cect -uesses eh: “* | Without spherasters (23.) ( Flesh-spicules euaster and oxyaster 28. } Flesh-spicules spirastrella ...........ccscseeeeeeee Flesh-spicules spirula and sigmata seen e ree eeneeee (27.) Without flesh-spicules Peewee eee eet a rene aeeeneee bundles divide the regular subdermal cavities into ectochonz or vestibules at the entrance of the inhalant canals Peer errr r eee e reer e errr ress ( | Om) at {canals eRe eCEUe ECOSOC OCOCOOeCe CSE e eee eee e errr rer) With spirastrellid flesh-spicules 29. 4 With sigmate flesh-spicules Without flesh-spicules Sete we rene ene ennee A Ree meee eee eee eweeee eee e ewww en eneee With polyact flesh-spicules Gl) { Without flesh-spicules eee eee eee Cec eee rere rere res 23. Plakinide. 24. Oscarellide. 26. (27.) . Geodide. 28. . Stellettide. 27. Theneide. 28. Tetillide. Tethyopsillide. The widened distal ends of the radial spicule- . Lethyde. . Sollasellide. 29. . Sptrastrellide, . Suberamatide. Suberitide. 35. Chondrillide. 36. Chondroside., 591 592 DR. R. VON LENDENFELD ON THE SysTEMATIC [Dee. 21, With proper spicules in the supporting skeleton. 30. (17.), Without proper spicules in the supporting BKGLStOR: Macatee ee cscce len sotont tee (31.) With uniformly distributed skeleton - reticu- lation and not very large subdermal cavities. 32. 30. The skeleton consists of a dense axial reticu- lation and isolated fibres extending from this to thesurface. Between these very extensive ( subdermal cavities are situated .............4. (33.) With gemmulz ; living in fresh water ......... 37. Spongillide. 82. { Withees BOMATIUID oo 5005, Soeeecediaveusentadeseeeee 34. Without flesh-spicules : fibres of the supporting skeleton not spined ............ssssecseesseesneee 38. Homorhaphide. 34. { Flesh-spicules sigmata or spiral ; no chele...... 39. Heterorhaphide. Flesh-spicules chele; when absent, fibres of | supporting skeleton HPUWIOU pecwarces se soe cnecoet 40, Desmacidonide. (33.)7 Nop chelie cies: Ae aie ee See 41, Avinellide. With small spherical chambers and opaque (31.) Pround-sapstance .2.....c--.se.cse- ocd sene-eosee== 35. ‘/ | With large sac-shaped chambers and trans- parent ground-substance ............:s.seeeeees (36.) 35 Without filaments in the ground-substance ... 37. : { with filaments in the ground-substance......... 38. 37 Skeleton-fibres with thin axial canal ............ 42. Spongide. 4 Skeleton-fibres tubular, with thick pith ..,...... 43. Aplysinide. (88.) Skeleton-fibre with thin axial canal ............ 44, Hircinide Skeleton-fibres with thin axial canal ; reticulate 45. Spongelida. (36.) 4 Skeleton-fibrestubular with thick pith; dendritic 46. Aplysillide. INoiskeleionte.s2-sc.scssacoseas .0> sarenehies.eeecee eee 47. Halisarcide. APPENDIX. LIST OF PUBLICATIONS RELATING TO THE SPONGES. (Explanations of the Abbreviations used are appended.) 1. #lianus, Claudius. [epi Zowyv. Liber 8, Cap. 16. 2. see Alexander, (On Hexactinellids.) Bull. Mus, C. Z. 1868, p. 367 (1868). 3. Aldrovandi, U. De reliquis animalibus exanguibus nempe de Mollibus, Crustaceis, Testaceis et Zoophytis libri quatuor. Bononia, 1606. Fol. (2nd ed. 1618; 8rd ed. 1623; 4th ed. 1642.) (1606-1642. ) 1886.] POSITION AND CLASSIFICATION OF SPONGES. 593 4. Allman, G.J. A new Order of Hydrozoa. Ann. M. N. H. ser. 4, vol. xiv. p- 237 (1874). [5.] ——. A new Order of Hydrozoa. Nature, vol. x. p. 251 (1874). 6. ——. A new Order of Hydrozoa. Tr. L. S. vol. i. p. 61 (1875). 7. Andrews, W. On Irish Sponges. Ann. M. N. H. ser. 4, vol. i. pp. 807, 308 (1868). 8. Aristoteles. [epi Gwwy icropias. Liber 1, cap. 1; Liber 5, cap. 16; Liber 8, cap. 1. 9. ——. Tlepi Zowy pogdiwy. Liber 4, Cap. 5. 10. Audouin, J. V., et Milne-Edwards. Résumé des recherches sur les animaux sans vertébres, faites aux iles Chausey. Ann. Sci. Nat. tom. xy. p. 5 (1828). Recherches pour servir a l'histoire naturelle du Littoral de la France, ou recueil de mémoires sur l’anatomie, la physiologie, la classification et les mceurs des animaux de nos cétes. ‘J'om.1. Paris (1832). 12. Austin, T. Note on Mr. Bowerbank’s paper on the genus Dunstervillia (Bwk.), with remarks on the Ischadites kinigii, the Tentaculites, and the Conularia. Ann. M. N. H. ser. 1, vol. xv. p. 406 (1845). 11. 13. Badeck, T. Red flints in the Chalk. Nature, vol. xxv. p. 529 (1882). 14. Baier, J. J. Oryctographia Norica, sive rerum fossilium et ad minerals regnum pertinentium in territorio Norimbergensi ejusque vicinia obser- vatarum succincta descriptio. (1708.) 15. Monumenta rerum petrif. Norimberge (1757). 16. Baird, S. F, American Sponges. United States Commission of Fish and Fisheries. Part 1. (1873.) 17. Balfour, F. M. The Morphology and Systematic Position of the Spongida. J. R, Micr. Sci. n,s. yol. xix. pp. 103-109 (1879). . Sur la morpholoyie et la position systématique des Eponges, (Extr.) Arch. Z, Expér. tom. viii. pp, 5-8 (1880). [18.] 19. Treatise on Comparative Embryology, vol. i. p. 18 (1880). 20. ——. On the structure and homologies of the germinal layers of the Embryo. @. J. Mier. Sci. vol. xx. p. 247 (1880). 21. ——. Larval Forms. Q. J. Micr. Sci. vol. xx. p. 381 (1880), 22. Balsamo-Crivelli,G. Memoria di aleuni Spongiari del golfo di Napoli. Atti Soc. Ital. yol. v. pp. 284-3802 (1863). Di aleuni organi speciali osservati in una Spugna. Wendic. Ist. Lomb. vol. iii. pp. 883-336 (1866). 24. Barrois, C. Spongiaires des sables d’Ostricourt et observations sur la phylogénie des Eponges. Ann. Soc. Géol. Nord, p. 71 (1875). 25. ——. Recherches sur le Terrain crétacé supérieur de ]’Angleterre et de YIrlande. (1876.) 26. ——. Mémoire sur l’Embryologie de quelques Eponges de la Manche (Sycandra, Halisarca, Verongia, Isodictya, Desmacidon), Ann. Sci. Nat, sér. 6, tom. ili. (1876). [27.] . Embryologie de quelques Eporges dela Manche. (Extr,) J. Anat, Phys. tom. xii. pp. 656-661 (1876). . On the development of Sponges. (Abstr.) Monthl. Mier. J. vol. xvi. pp. 254-256 (1876). Embryologie de quelques Eponges de la Manche. (Extr.) Budi. Sciént. du dép. du Nord, tom. viii. pp. 151-155 (1877). 30. ——. Sur les Dictyospongide des Psammites des Chondroz. Ann. Soe. Géol. Nord, tom, xi. p. 80 (1883), Proc. Zoou. Soc.—1886, No. XXXIX. 39 23. [28.] [29.] 594 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, - Bauhin, J. Hist. fontis Bollensis. Montisbelgardi (1598). 2. Bauhin, J., et Cherler, J. H. Hist. plant. Ebroduni (1651). 3. Bauhin, K. Pinax Theatri Botanici. Basilex, Helvet. (1623). . Bell, T. Remarks on the animal nature of Sponges. Zool. Journ. vol. i. p. 202 (1824). 5. Bellamy, J.C. Natural History of South Devon. London (1840). . Belon, A, De aquatilibus. Liber ii. Parisiis (1553). . Beltremieux. Faune du département de la Charente-Inférieur. (1860.) . Beneaume. Spongia fluviatilis fragilis et piscem olens. Mém. Acad. Sci, Paris, p. 231 (1814). J. Beneden, E. Van. Die Cclenteraten-Natur der Spongien. Ber. Vers. Nat. Hannover, p. 263 (1864). . Benett, E. Catalogue of the organic remains of the county of Wilts. Warminster (1831). . Bennett, George. On the Euplectella aspergillum, Owen, or “ Venus’s Flower-Basket.” Proc. R. Soc. Tasm. pp. 59-65 (1875). . Bertolini, A. Rariorum Italix plantarum dec. 3 accedit specim. zoophyt. Portus Lune. Piss (1810). Sopra alcuni paradox nat. (Spongitarii) nel golfo della Spezia. Modena (1832). . Bianchi, G. De conchis minus notis. Ed.ii. Rome (1760). . Bianconi, G.G. Sopra alcuni Zoofiti descriti sotto i nomi di Cliona celata, ete. Nuovi Ann. Sci. Nat. vol. vi. p. 455 (1841). . Bigsby, J. J. Thesaurus Siluricus. London (1868). . ——. Thesaurus Devonico-Carboniferus. London (1878). . Billings, E. Paleozoic fossils. Geol. Surv. Canada, Fasc. i. 1-5. Mon- treal (1861-1865). On some new or little-known Fossils from the Silurian and Devonian Rocks of Ontario. Canadian Nat. and Geol. n.s. vol. vii. (1875). . Blainville, M.H.D.de. Planches. ii. Partie, Zoologie, Vers et Zoo- phytes. Dictionnaire Sci. Nat., Paris et Strasbourg (1816-1839). ._—. Eponges. Dictionnaire Sci. Nat. tom. xy. p. 93 (1819). . ——. Zoophytes. Dictionnaire Sci. Nat. tom. |x. p. 1 (1830). . —--—. Manuel d’Actinologie et de Zoophytologie. Paris (1834-1837). . Barboza du Bocage, J. V. Note sur la découverte d’un Zoophbyte de la famille Hyalocheetides sur la cote du Portugal. P. Z. 8.1864, pp. 265- 269 (1864). .—. Sur habitat du Hyalonema lusitanicum. P. Z. S. 1865, pp. 662- 663 (1865). . On Hyalonema lusitanicwm. Ann, M,N. H. ser. 3, vol, xx. pp. 123- 127 (1867). . Notes on Hyalonema boreale and a new Genus of Sponges. Ann. M. N. H. ser. 4, vol. ii. pp. 36-38 (1868). Eponges siliceuses nouvelles de Portugal et de Vile St. Jago: Podo- spongia lovenii, Reniera(?) grayi, Discodermia polydiscus, Latrunculia ceratera. J. Sci. Lisb, tom. li, pp. 159-161 (1870). . Sur existence de la Holtenia carpenteri, Wyville Thomson, dans les cétes du Portugal. J. Sci. Lisb. tom. iii. pp. 69-70 (1870). . Boerhave, H. Index alter. plant. hort. Lugd. Batay. (1720). - Bosc, L. A. G. Histoire Naturelle des Vers. Paris, tom. iii. (1802). 2. ——. Histoire Naturelle des Vers. Paris, tom. iii. 2nd. edit. (1827). . Bourguet, L., et Cortier, P. ‘Traité des pétrefactions. Paris (1742). 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 595 64, Bowerbank, J.S. On the Keratose or Horny Sponge of commerce. Mier. J. vol. i. pp. 8-11 (1841). 65. ——. Descriptions of three species of Sponge containing some new forms of organization. Mier. J. vol. i. pp. 161-162 (1841). 66. Observations on a Keratose Sponge from Australia. Ann. M. Ny. H. ser. 1, vol. vii. p. 129 (1841). [67.] Sur les Kératoses ou Eponges cornées du commerce. (Trad.) L’Jn- stitut, tom. ix. no. 582, p. 137 (1841). 68. On the spongeous origin of Mossagates and other siliceous bodies. Ann. M. N. H. ser. 1, vol. x. p. 9 (1842). 69. ——. On the spongeous origin of Mossagates and other siliceous bodies. Ann, M. N. H. ser. 1, vol. x. p. 84 (1842). 70. ——. On the Keratose or Horny Sponges of commerce. Tr, 2. Micr. Soc. vol. i. pp. 32-39 (1844). 71. On three species of Sponge, containing some new forms of organi- zation. Tr. R. Micr. Soc. vol. i. pp. 63-76 (1844), 72. Description of a new genus of Calcareous Sponges (Dunstervillia). Ann. M. N. H. ser. 1, vol. xv. pp. 297-300 (1845). 73. ——. Observations on the Spongiade. Ann. M. N. H. ser. 1, vol. xvi. p. 400 (1845). 74. ——. On the Ciliary Action in Spongiade. Tr. R. Mier. Soc. vol. ili. p- 187 (1852). 75. ——. Further Report on the Vitality of Sponges. Rep. Brit. Assoc. 1857, pp. 121-125 (1857). 76. are ete the Vital Powers of the Spongiade. Rep. Brit. Assoc. 1857, p. 438 57). 77. ——. On the Anatomy and Physiology of the Spongiade. P. R. Soc. vol. viii. p. 573 (1857). On the Anatomy and Physiology of the Spongiade. Ann, M. N. H. ser. 2, vol. xx. p. 298 (1857). (79.] ——. Sur les forces vitales des Spongiadées. (Trad.) L’Jnsti¢ut, tom, xxy. no. 1208, p. 63 (1857). [80.] ——. Seconde rapport sur la vitalité des Spongiadées. (Trad.), L’Jn- stitut, tom. xxvi. no. 1266, p. 121 (1858). 81. ——. On the Anatomyand Physiology of the Spongiade. PartI. Phil. Tr. vol. exlviii. p. 279 (1858). 82. Further Report on the Vitality of Sponges. J. R. Micr. Soc, yol. vi. pp. 78-79 (1858). 83. ——. On the Organization of, Grantia ciliata, Tr. R. Micr. Soc. n. 8, vol. vil« pp- 79-84 (1859), 84. Ra “oe the fibre in Keratose Sponges. Q. J. Micr. Sci. vol. viii. p. 187 860). 85. On the Anatomy and Physiology of the Spongiade. II. P. R. Soe. vol. xi. pp. 872-375 (1862). 86. On the Anatomy and Physiology of the Spongiade. II. Phil. Tr. vol. clii. pp. 747-836 (1862). 87. On the Anatomy and Physiology of the Spongiade. Part III. Phil. Tr, vol. cli. p. 1087 (1862). 88. ——. On the Anatomy and Physiology of the Spongiadw. P. R. Soc, vol. xii. pp. 146-148 (1863). 89. This En Monograph of the Spongillide. P. R. Soc. yol. xii. pp. 440-472 (1863). 90. ——. A Monograph of the British Spongiade. (Ray Society.) Vol. I. (1864). 39* 596 DR«R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 91. Bowerbank, J.S. Description of two American Sponges (Zethea his- pida, Spongilla dawsonii). Can. Nat. n. 8. vol. i. pp. 304-307 (1864). 92. ——. A Monograph of the British Spongiadz. (Ray Society.) Vol. II. (1866.) On Hyalonema mirabilis, in reply to Dr. Gray. Ann. Ve NAA 93. : ser. 8, vol. xviii. pp. 397-401 (1866). 94. Two Sponges new to Science—Halichondria couchi, Microciona fron- dosa. Rep. Brit. Assoc. 1867, pp. 285-286 (1867). 95. ——. On Hyalonema mirabile. P. Z. S. 1867, pp. 18-34 (1867). 96. ——. Additional observations on Hyalonema mirabile. P.Z. S. 1867, pp. 350-351 (1867). 97. ——. On Aleyoncellum (Euplectella) speciosum, Quoy and Gaimard. P. Z. 8. 1867, pp. 351-859 (1867). 98. ——. On Hyalonema lusitanicum. P. Z. 8. 1867, pp. 901-907 (1868). 99. ——. Observations on Dr. Gray’s “ Notes on the Arrangement of Sponges, with the Description of some New Genera.” P. Z. S. 1868, pp. 118- 137 (1868). 100. ——. A Monograph of the Siliceo-fibrous Sponges. Part I. P. Z. S. 1869, pp. 66-100 (1869). 101. ——. A Monograph of the Siliceo-fibrous Sponges. Part II. P.Z.S. 1869, pp. 823-351 (1869). 102. ——. On Dr. Gray’s Genus Theonella (Dactylocalyx). P.Z.S. 1869, pp. 389, 390 (1869). 103. ——. On the generic name Alcyoncellum, and in reply to Dr, Gray’s “« Observations on Sponges and on their Arrangement and Nomenclature.” Ann. M. N. H. ser. 4, vol. iii. pp. 84-87 (1869). 104. ——. Observations on Mr. Carter’s paper ‘‘On two new Sponges from the Antarctic Sea, &e.” Ann. M. N. H. ser. 4, vol. x. pp. 58-61 (1872). 105. ——. Contributions to a general History of the Spongiade. Part I. ; P. Z. 8. 1872, pp. 115-129 (1872). 106. ——. Contributions to a general History of the Spongiade. Part II. P. Z. 8. 1872, pp. 196-202 (1872). 107. ——. Contributions toa general History of the Spongiade. Part III. P. Z. 8. 1872, pp. 626-684 (1872). Reply to Dr. J. E. Gray’s Observations on certain Species of Sponges described in the ‘ Proceedings of the Zoological Society’ for 1878. Ann. M,N. H. ser. 4, vol. xii. pp. 488-491 (1873). 109. ——. Contributions to a general History of the Spongiade. Part IV. P. Z. 8. 1873, pp. 8-25 (1878). 110 Report on a Collection of Sponges found at Ceylon by E. W. H. Holdsworth, Esq. P. Z. 8S. 1873, pp. 25-82 (1873). 111 Contributions to a general History of the Spongiade. Part V. P. Z. 8. 1873, pp. 819-333 (1873). 112. ——. Contributions to a general History of the Spongiade. Part VI. P. Z. 8. 1874, pp. 298-305 (1874). 113. ——. A Monograph of the British Spongiadex. (Ray Society.) Vol. IIT. (1874). 114. ——. -A Monograph of the Siliceo-fibrous Sponges. Part III. P. Z. 8. 1875, pp. 272-281 (1875). 115, ——. Contributions to a general History of the Spongiade. Part VII. P. Z. 8. 1875, pp. 281-296 (1875). 116. . A Monograph of the Siliceo-fibrous Sponges. Part IV. P. Z. 8. 1875, pp. 503-509 (1875). 117. A Monograph of the Siliceo-fibrous Sponges. Part V. P. Z. 8. 1875, pp. 558-565 (1875). ——_ 1886.] POSITION AND CLASSIFICATION OF SPONGES. 597 118. Bowerbank, J. S. Further observations on Alcyoncellum speciosum, Quoy et Gaimard, and Hyalonema mirabilis, Gray, P. Z. S. 1875, pp. 607-610 (1875). 119. ——. A Monograph of the Siliceo-fibrous Sponges. Part VI. P. Z. 8, 1876, pp. 535-540 (1876). 120. ——. Contributions toa general History of the Spongiade. Part VIII. P. Z. 8. 1876, pp. 768-775 (1876). 121. Description of five new Species of Sponges discovered by A. B. Meyer on the Philippine Islands and New Guinea. (Opus posthum.) P, Z. 8. 1877, pp. 456-464 (1877). 122. A Monograph of the British Spongiadx, by the late Dr. Bower- bank ; edited, with additions, by the Rev. A. M. Norman. (Ray Society.) Vol. IV. (1882). 123. Brandt, J. F. Extrait d’un mémoire: de noya polyporum familia aoe nomine designanda. Bull. Ac. Pétersb. vol. xvi. p. 65 (1850). 124. ——. Symbole ad polypos Hyalochztidium spectantes, Petropoli (1859). 125. Brandt, K. Ueber das Zusammenleben von Thieren und Algen. Ver. Phys. Ges. Berlin, no. 5, p. 22 (1881). 126. ——. Ueber die morphologische und physiologische Bedeutung des Chlo- rophylls bei Thieren. Arch, Anat. Phys. p. 125 (1882). 127. ——. Ueber die morphologis-he und physiologische Bedeutung des Chlo- rophylls bei Thieren. 2. Artikel. MT. 2. Stat. Neap. Bd, iv. pp. 191- 302 (1883). ‘ 128. Braun, H.G. Lethxa Geognostica. 2nded. Stuttgart (1834-38), 129. ——. Lethxa Geognostica. 3rded. Stuttgart (1846-56). 130. ——. Index Palxontologicus. 1 Abth. Stuttgart (1848). 131. ——. Index Paleontologicus. 2 Abth. Stuttgart (1849), Bronn’s Klassen und Ordnungen des Thierreichs. I. Amorphozoa. Leipzig (1859). 133. Braun, M. Ueber die Geschlechts verhiiltnisse bei Halisarca lobularis, O.Schm. Zool. Anz. vol. iv. pp. 232-234 (1881). 134, Brotherus. Spongilla. Meddel. af. Soc. pro Fauna et Flora Fennica, vol. ii. p. 168 (1878). 135. Bruder, K. Zur Kenntniss der Juraablagerung von Sternberg bei Zeidler in Bohmen. SB. Ak. Wien, 1881, p. 47 (1881). 136. ao W. On the Paramandra. Tr. Geol. Soc. vol. ix. p. 412 (1817). 137. Burg, van der. Beschrijving van een exemplar Euplectella aspergillum. ase Tijdschrift voor Nederlandsch Indié, vol. xxxi. pp. 473-475 138. Biitschli, O. Ueber die Stellung der Spongien. Z. wiss, Zool. Bd. xxx. p- 221 (1878). Bemerkungen zur Gastratheorie. Morph. Jahrb. Bd. 9, pp. 416- 427 (1884). [{140.] ——. Remarks on the Gastrea Theory. (Transl.) Ann. M. N. H. ser. 5, vol. xiii. pp. 873-383 (1884). 141. Buxbaum, J.C. Nova Plantarum genera. Comm. Acad. Petropol. ii. p- 343 (1729). 139. 142. Capellini, Dr., und Dr. Pagenstecher. Mikroscopische Untersuch- ungen iiber den innern Bau einiger fossilen Schwimme. Z. wiss. Zool, Bd. x. pp. 364-372 (1860) 143, Carpenter, Dr. On Hexactinellids. Ann, M. N, H. ser. 4, vol. ii. p. 820 (1868). 598 DR. R. VON LENDENFELD ON THE SysTEMATIC [Dec. 21, 144. Carpenter, Dr., and Wyville Thomson. On Hexactinellids, Ann, M., N. H. ser. 4, vo). iv. p. 120 (1869). 145. ——. On Hexactinellids. Ann. M. N. H. ser. 4, vol. iv. p. 281 (1869). 146. ——, Jeffreys, and W. Thomson. Report on the Dredging Expedi- tion of the ‘Porcupine. P. R. Soc. vol. xviii. pp. 397-492 (1869). 147. Report on the Dredging Expedition of the ‘Porcupine. P. R. Soc. vol. xix. pp. 146-221 (1870). [148.] —— and W. Thomson. Sur Eponges. Arch, Sci. Nat.tom. xli. pp. 81—- 83 (1870). 149, Carter, H. J. Notes on the Species, Structure, and Animality of the Freshwater Sponges in the tanks of Bombay. Ann. M. N. H. ser. 2, vol. i. pp. 303-311 (1848). 150, ——. A descriptive account of the Freshwater Sponges (Genus Spon- gilla) in the Island of Bombay, with Observations on their Structure and Development. Ann. M. N. H. ser. 2, vol. iv. pp. 81-100 (1849). 151. . A descriptive account of the Freshwater Sponges (Genus Spongilla) in the Island of Bombay, with Observations on their Structure and Development. J. Bombay Branch R. Asiatic Soe. vol. iii. p. 29 (1849). 152. ——. Zoosperms in Spongilla. Ann. M. N. H. ser. 2, vol. xiv. pp. 834— 336 (1854). 158. On the Ultimate Structure of Spongilla, and Additional Notes on Freshwater Infusoria. Ann. M. N. H, ser. 2, vol. xx. pp. 21-41 (1857). 154. On a Variety of Spongilla meyeni from the River Exe, Devonshire, Ann, M.N. H. sev. 4, vol. i. p. 247 (1868). 155. -—. Description of a Siliceous Sand-Sponge found on the south-east coast of Arabia. Ann. M. N. H. ser. 4, vol. iii. p. 151 (1869). 156. Calcareous Sponges (Central Canal in Spicules). Ann. M. N. H. ser. 4, vol. iii. p. 466 (1869). 157, Descriptive account of four Subspherous Sponges, Arabian and British, with general observations. Ann, M. N. H. ser. 4, vol. iv. p. 1 (1869). 158. ——. On Grayella cyathophora, a new genus and species of Sponge. Ann. M. N. H. ser. 4, vol. iv. p. 189 (1869). 159. ——. Note on the Sponges Grayella, Osculina, and Cliona. Ann. M. N. H. ser. 4, vol. v. p. 73-83 (1870). On Haliphysema ramulosa, Bowerbank, and the Sponge-spicules of Polytrema. Ann. M. N. H. ser. 4, vol. v. pp. 389-392 (1870). 161. ——. On two new species of Subsphxrous Sponges. Ann. M. N. H. ser. 4, vol. vi. p. 176 (1870). 160. 162. On the Ultimate Structure of Marine Sponges. Ann. M. N. H. ser. 4, vol. vi. pp. 829-342 (1870). 163. A descriptive account of three Pachytragous Sponges growing on the rocks of the South Coast of Devon (Dercitus, Stelletta). Ann. M. N, HH, ser. 4, vol. vii. pp. 1-15 (1871). 164. On Fossil Sponge-spicules of the Greensand compared with those of existing Species. Ann. M. N. H. ser. 4, vol. vii. pp. 112-141 (1871). 165. On two undescribed Sponges (Ectyon, Acarnus) and two Esperiade from the West Indies; also on the Nomenclature of the Calcisponge, Clathrina, Gray. Ann, M. N. H. ser. 4, vol. vii. pp. 268-283 (1871). 166. ——. Discovery of the Animal of the Spongiadz confirmed, Ann. M. NN. H. ser. 4, vol. vii. p. 445 (1871). 167. ——. A description of two new Calcispongie (Trichogypsia, Leuconia), to which is added confirmation of Prof. James-Clark’s Discovery of the True Form of the Sponge-cell (Animal), and an Account of the Polype-like Pore-area of Cliona coralloides contrasted with Prof. E, hie. ele 1886.] POSITION AND CLASSIFICATION OF SPONGES, 599 Hiickel’s View on the Relationship of the Sponges to the Corals, Ann, M. N. H. ser. 4, vol. viii. pp. 1-28 (1871). 168. Carter, H. J. Description and Illustration of a new Species of Tethya, with observations on the Nomenclature of the Tethyade. Ann. M,N. H. ser. 4, vol. viii. pp. 99-106 (1871). 169. . Parasites of the Sponges. Ann. M. N. H. ser. 4, vol. viii. pp. 330- 332 (1871). 170. Additional information on the structure of Tethya dactyloidea, Cart. Ann. M. N. H. ser. 4, vol. ix. pp. 82-84 (1872). 171. ——-. On two new Sponges from the Antarctic Sea, and on a new Species of Tethya from Shetland (Zethya antarctica, Rossella antarctica): to- gether with observations on the Reproduction of Sponges, commencing from Zygosis of the Sponge-animal. Ann. M. N. H. ser. 4, yol. ix. pp. 409-436 (1872). 172. . Proposed name for the Sponge-animal, viz. “‘ Spongozoon” ; also on the origin of Thread-cells in the Spongiade. Ann. M. N. H. ser. 4, vol. x. pp. 43-51 (1872). 173. ——. Description, with illustrations, of a new species of Aplystna from the N.W. coast of Spain. dun. M,N. H. ser. 4, vol. x. pp. 101-110 (1872). 174. ——. Description of two new Sponges from the Philippine Islands (Meyenia, Crateromorpha). Ann. M. N. H. ser. 4, vol. x. pp. 110-114 (1872). 175. . Answer to Dr. Bowerbank’s ‘‘Obseryations on Mr. Carter’s Paper &c.,” in the last number of the ‘ Annals.’ Ann. M. N. H. ser. 4, vol. x. pp- 141-142 (1872). 176. Description of Labaria hemispherica, Gray, a new species of Hexactinellid Sponge, with observations on it and the Sarco-hexacti- nellid Sponges generally. Ann. M. N. H. ser. 4, vol. xi. pp. 275-286 (1873). 177. ——. Points of distinction between the Spongide and the Foraminifera, Ann. M. N. H. ser. 4, vol. xi. pp. 351-356 (1873). 178. On two new species of Gumminee (Corticium abyssi, Chondrilla australiensis), with special and general observations. dun. M. N. H. ser. 4, vol. xii. pp. 17-30 (1878). 179. On the Hexactinellide and Lithistide generally, and particularly on the Aphrocallistide, Aulodictyon, and Farree, together with Facts elicited from their Deciduous Structures, and Descriptions respectively of three new Species (I.). Ann. M. N. H. ser. 4, vol. xii. pp. 849-373 (1873). 180. ——. On the Hexactinellide and Lithistide generally, and particularly on the Aphrocallistide, Aulodictyon, and Farree, together with Facts elicited from their Deciduous Structures, aud Descriptions respectively of three new Species (II.). Ann. M. N. H. ser. 4, vol. xii. pp. 487-472 (1878). 181. ——. On the Spongozoa of Halisarca Dujardinii. Ann. M. N. H. ser. 4, vol. xii. pp. 315-316 (1874). 182, ——. On Halisarca lobularis, Schmidt, off the south coast of Devon with observaions on the Relationship of the Sponges to the Ascidians and Hints for Microscopy. Ann. M. N. H. ser. 4, vol. xiii. pp. 433- 440 (1874). 183. ——. On Microciona. Ann. M. N. H. ser. 4, vol. xiv. p. 45 (1874). 184. On the Nature of the Seed-like Body of Spongilla ; on the Origin or Mother-cell of the Spicule ; and on the presence of Spermatozoa in the Sponges. Ann. M. NV. H. ser. 4, vol. xiv. pp. 97-111 (1874). 185. Descriptions and Figures of Deep-sea Sponges and their Spicules from the Atlantic Ocean, dredged up on board H.M.S. ‘ Porcupine,’ 600 DR, R. VON LENDENFELD ON THE SysTeEMATIC [Dec. 21, chiefly in 1869; with Figures and Descriptions of some remarkable Spicules from the Agulhas Shoals and Colon, Panama. I. Ann, M,N. H. ser. 4, xiv. pp. 207-222 (1874). 186. Carter, H. J. Descriptions and Figures of Deep-sea Sponges and their Spicules from the Atlantic Ocean, dredged up on board H.MLS. ‘ Poreu- pine,’ chiefly in 1869; with Figures and Descriptions of some remarkable Spicules from the Agulhas Shoals and Colon, Panama. IL. Ann. M. N. H. ser. xiv. pp. 245-257 (1874). Development of the Marine Sponges from the earliest recognizable appearance of the Ovum to the perfected Individual. I. Ann, M..N. H, ser. 4, vol. xiv. pp. 321-337 (1874). Development of the Marine Sponges from the earliest recognizable appearance of the Ovum to the perfected Individual. II. Ann, M.N.H. ser. 4, vol. xiv. pp. 389-406 (1874). Further instances of the Sponge-spicule in its Mother-cell. Ann. M. N. H. ser. 4, vol. xiv. pp. 456-458 (1874). 190. ——. On the Genus Rossella (a Hexactinellid Sponge), with the Descrip- tions of three new Species. Ann. M. N. H. ser. 4, vol. xy. pp, 113-122 (1875). 191. ——. Notes Introductory to the Study and Classification of the Spongida. I. Anatomy and Physiology. Ann. M. N. H. ser. 4, vol. xvi. pp. 1-41 (1875). Notes Introductory to the Study and Classification of the Spongida. TI. Proposed Classification of the Spongida (I.). Ann. M. N. H. ser. 4, vol. xvi. pp. 126-145 (1875). Notes Intreductory to the Study and Classification of the Spongida. II. Proposed Classification (II.). Ann. M. N. H. ser. 4, vol. xvi. pp. 177-200 (1875). Descriptions and Figures of Deep-sea Sponges and their Spicules from the North Atlantic Ocean, dredged up on board H.M.S. ‘ Porcu- pine” Ann. M. N. H. ser. 4, vol. xviii. pp. 226-240 (1876). . Description and Figures of Deep-sea Sponges and their Spicules from the North-Atlantic Ocean, dredged up on board H.M.S. ‘ Poreu- pine.” Ann. M. N. H. ser. 4, vol. xviii. pp. 807-324 (1876). 196, ——. Descriptions and Figures of Deep-sea Sponges and their Spicules from the North-Atlantic Ocean, dredged up on board H.M.S. ‘ Porcu- pine’ Ann. M. N. H. ser. 4, vol. xviii. pp. 388-410 (1876). 187. 188. 189. 192. 193. 194. 195. 197. Descriptions and Figures of Deep-sea Sponges and their Spicules from the North- Atlantic Ocean, dredged up on board H.M.S. ‘ Poreu- pine” Ann. M. N. H. ser. 4, vol. xviii. pp. 458-473 (1876). 198. On two Vitreo-hexactinellid Sponges (Hurete farreopsis, n. sp., and Myliusia grayi, Bk.). Ann, M. N. H. ser. 4, vol. xix. pp. 121-131 (1877). 199. ——. Description of Mauricea. Ann. M. N. H. ser. 4, vol. xix. p. 174 (1877). 200. Note on the “ Tubulations Sableuses” of the étage Bruxellien in the environs of Brussels. Ann. M. NV. H. ser. 4, vol. xix. pp. 382-393 (1877). 201. Arctie and Antarctic Sponges. Ann. M. N. H. ser. 4, vol. xx. pp. 38-43 (1877). 202. ——. Ona Fossil species of Sarco-hexactinellid Sponge allied to Hya- lonema. Ann. M. N. H. ser. 4, vol. xx. pp. 176-178 (1877). 203. ——. Mr. James Thomson’s Fossil Sponges from the Carboniferous System of the South-west of Scotland. Ann. M. N. H. ser. 5, vol. i. pp. 128-143 (1878). 204. ——. Position of the Sponge-spicule in the Spongida ; and Postscript on the identity of Sguamulina scopula with the Sponges. Ann. M. N. A. ser. 5, vol. i. pp. 170-174 (1878). ee 1886. ] POSITION AND CLASSIFICATION OF SPONGES. 601 205. Carter, H. J. Emendatory Description of Purisiphonia clarkei, Bk., a hexactinellid fossil Sponge from N.W. Australia, Ann. M. N. H. ser. 5, vol. i. pp. 376-879 (1878). On Calcareous Hexactinellid Structures in the Devonian Limestone, large fossil Hydrozoic Coralla from the Chalk, and further observations on the replacement of Silex by Calcite. Ann. M. N. H. ser. 5, vol. i. pp- 412-419 (1878). On Teichonia, a new Family of Calcareous Sponges, with descrip - tions of two species. Ann. M. N. H. ser. 5, vol. ii. pp. 85-40 (1878). . Parasites of the Spongida. Ann, M. N. H. ser. 5, vol. ii. pp. 157- 172 (1878). 209. ——. Note on Tethya muricata, Bowerbank. Ann. M. N. H. ser. 5, vol. ii. pp. 174-177 (1878). 210. On Holastrella, a Fossil Sponge of the Carboniferous era, and on Hemiastrella, a new species of recent Sponge. Ann. M. N. H. ser. 5, vol. ili. pp. 141-150 (1879). 211, Contributions to our Knowledge of the Spongida. Ann. M. N. H. ser. 5, vol. iii. pp. 284-304 (1879). 212. Contributions to our Knowledge of the Spongida. Ann. M. N. H. ser. 5, vol. iii. pp. 343-360 (1879). 215. . On the Nutritive and Reproductive Processes of Sponges. Ann. M. N. H. ser. 5, vol. iv. pp. 374-386 (1879). 214 . Note on the so-called “ Farringdon (Coral-Rag) Sponges” (Calci- spongie, Zittel). Ann. M. N. H. ser. 5, vol. iv. pp. 431-437 (1879). 215, On a new species of excavating Sponge (Alectona millari), and on a new species of Rhaphidotheca (R. affinis). J. R. Micr. Soe. vol. ii. pp- 448-449 (1879). 216. ——. Spongide from Kerguelen’s Island. Phil. Trans. yol. elxviii. pp. 286-288 (1879). 217. . Ona new genus of Foraminifera; and Spiculation of an unknown Sponge. Zr, R. Mier. Soc. vol. ii. pp. 500-502 (1879). 218. Report on Specimens dredged up from the Gulf of Manaar and presented to the Liverpool Free Museum by Capt. W. H. Cawne Warren. Ann. M. N. H. ser. 5, vol. vi. p. 35 (1880). 219. On Fossil Sponge-spicules from the Carboniferous strata of Ben Bulben, near Sligo. Ann. M. N. H. ser. 5, vol. vi. pp. 209-214 (1880). [220.] ——. Report on Sponges dredged in the Gulf of Manaar. (Abstr.) P. Liverp. Soc. vol, xxxiy. p. 273 (1880). . List of fourteen Species of Sponges dredged at Falmouth. Tr. Birmingham Soe. vol. 1880, p. 59 (1880). 222, ——, and W.S.M. D’Urban. On the Zoology of the Barents Sea. Ann. M. N. H. ser. 5, vol. vi. p. 253 (1880). 221. 223. Sponges. Including list of Sponges dredged by the Birmingham Natural History and Microscopical Society, Falmouth Excursion, 1879; depth 15-20 fathoms. Midland Naturalist, p. 190 (1880). 224. History and Classification of the known species of Spongilla. Ann. M. N. H. ser. 5, vol. vii. pp. 77-107 (1881). 225. ——. On Spongilla cinerea. Ann. M. N. H. ser. 5, vol. vii. pp. 263, 264 (1881). 226. ——. Supplementary Report on the Specimens dredged up from the Gulf of Manaar, together with others from the Sea in the vicinity of the Bass Rocks and from Bass’s Straits respectively, presented to the Liverpool Free Museum by Capt. H. Cawne Warren. Ann. M. N. H. ser. 5, vol. vii. p. 361 (1881). Contributions to our Knowledge of the Spongida.—Order II. Ceratina, Ann. M. N. H. ser. 5, yol. viii. pp. 101-112 (1881). 602 DR. R. VON LENDENFELD ON THE SYSTEMATIC [Dec. 21, 228. Carter, H.J. On the Development of the Fibre in the Spongida, Ann. M.N. Z. ser. 5, vol. viii. pp. 112-120 (1881), 229, ——. On Spongiophaga in Spongilla, Ann. M. N. H. ser. 5, vol. viii. p. 222 (1881). 230, Contributions to our Knowledge of the Spongida.—Order I. Car- nosa. Ann. M.N. H. ser. 5, vol. viii. pp. 241-259 (1881). 231. waaay Spongiophaga pottsi. Ann. M. N. H. ser. 5, vol. viii. p. 354 1881). 232, Addendum to our Knowledge of the Carnosa, Ann. M. N. H. ser. 5, yol. viii. p. 450 (1881). 233. Some Sponges from the West Indies and Acapulco, in the Liverpool Free Museum, described, with general and classificatory remarks, Ann. M.N. H. ser. 5, vol. ix. pp. 260-301 (1882). 234, Some Sponges from the West Indies and Acapulco, in the Liverpool Free Museum, described, with general and classificatory remarks. Ann. M. N. H. ser. 5, vol. ix. pp. 346-369 (1882). 235. Form and Nature of the Cirrous Appendages on the Statoblast of Carterella latitenta, Potts, &c., originally designated Spongiophaga pottst. Ann. M.N. H. ser. 5, vol. ix. pp. 390-396 (1882). [285.] ——. Form and Nature of the Cirrous Appendages on the Statoblast of Carterella latitenta, Potts, &c., originally designated Spongiophaga pottsi. (Abstr.) J. R. Mier. Soc. vol. ii. p. 350 (1882). 237. ——. New Sponges, observations on old ones, and a proposed new group (Phleodictyina). Ann. M. N. H. ser. 5, vol. x. pp. 106-125 (1882). Spermatozoa, Polygonal Cell-structure, and the Green Colour in Spongilla, together with a new species. Ann. M, N. H. ser. 5, vol. x. pp. 362-372 (1882). Further observations on the so-called “‘ Farringdon Sponges” (Cal- cispongie, Zittel), followed by a description of an existing species of a like kind (Leucetta clathrata,n.sp.). Ann. M. N. H. ser. 5, vol. xi. pp. 20-87 (1883). . Contributions to our Knowledge of the Spongida.—Pachytragida. Ann. M. N. H. ser. 5, vol. xi. pp. 344-369 (1883). A new genus of Sponges (Monanchora clathrata). Ann. M. N. H, ser. 5, vol. xi. pp. 369-370 (1883). On the Microscopic Structure of thin slices of Fossil Calcispongiz. Ann. M. N. H. ser. 5, vol. xii. pp. 26-80 (1888). On the Presence of Starch-Granules in the Ovum of the Marine Sponges, and on the Ovigerous Layer of Suberites domuncula, Nardo. Ann. M. N. H. ser. 5, vol. xii. pp. 80-36 (1883). Contributions to our Knowledge of the Spongida. Ann. M. N. H. ser. 5, Vol. xii. pp. 308-329 (1883). Spicules of Spongilla in the Diluvium of the Altmthl Valley, Ba- varia. Ann. M. N. H. ser. 5, vol. xii. pp. 329-333 (1883). 246. ——. Remarks on Dr. Vejdovsky’s Paper [vide infra]. Ann. M. N. H. ser. 5, vol. xiii. p. 99 (1884). 238. 239. 247. Generic Characters of the Sponges described in Mr. Carter’s “ Contributions to our Knowledge of the Spongida,” Ann. M. N. H. ser, 5, vol. xii. p, 308 (1883). Ann. M. N. H. ser, 5, vol. xiii. pp. 129- 130 (1884). 248, —-. On Grantia ciliata, var. spinispiculum. Ann. M. N. H. ser. 5, vol, xiii. pp. 153-163 (1884). 249. The Branched and Unbranched Forms of the Freshwater Sponges considered generally. Ann. M. N. H. ser. 5, vol. xiii. pp. 269-273 (1884). 1886.] POSITION AND CLASSIFICATION OF SPONGES. 603 250. Carter, H. J. Note on the assumed relationship of Parkeria to Stro- matopora, and on a microscopic section of Stromatopora mamillata, Fr. Schmidt. Ann. M. N. H. ser. 5, vol. xiii. pp. 353-356 (1884). Catalogue of the Marine Sponges collected by Mr. Jos. Willcox on the West Coast of Florida. P. dc. Philad. 1884, pp. 202-209 (1884). 252. ——. On the Spongia coriacea of Montagu = Leucosolenia coriacea, Bwk., together with a new Variety of Leucosolenia lacunosa, Bwk., elucidating the Spicular Structure of some of the Fossil Calcispongie ; followed by Illustrations of the Pin-like Spicules on Verticillites helvetica, De Loriol. Ann. M. N. H. ser. 5, vol. xiv. p. 17 (1884). 251. 253. - Note on Spongilla fragilis, Leidy, and a new Species of Spongilla [mackayi| from Nova Scotia. Ann. M. N. H. ser. 5, vol. xv. pp. 18-20 (1885). 254, Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M. N. H. ser. 5, vol. xv. pp. 107-117 (1885). 255. ——. Mode of Circulation in the Spongida. Ann. M. N. H. ser. 5, vol. xv. pp. 117-122 (1885). New Sponges from South Australia. (Abstr.) J. R. Mier. Soe. ser, 2, vol. vy. p. 465 (1885). Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. dan. M. N. H. ser. 5, vol. xv. pp. 196-222 (1885). 258, ——. Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M, N. H. ser. 5, vol. xv. pp. 801-821 (1885). [259.] ——. Circulationin Spongida. (Abstr.) J. R Micr. Soc. ser. 2, vol. vy. pp. 816-817 (1885). 260. ——. Report on a Collection of Marine Sponges from Japan, made by Dr. J. Anderson, F.R.S. Ann. M. N. H. ser. 5, vol. xv. pp. 887-406 (1885). [256.] 257. 261. . Ona variety of the Freshwater Sponge, Meyenia fluviatilis, Ann. M. N. H. ser. 5, vol. xv. pp. 453-456 (1885). 262. . Ona variety of the Freshwater Sponge Meyenia fluviatilis, from Florida. Ann. M. N. H. ser. 5, vol. xvi. pp. 179-181 (1885). 263. Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M. N. H. ser. 5, vol. xvi. pp. 277-294 (1885). 264. ——. Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia, dan. M. N. H. ser. 5, vol. xvi. pp. 847-368 (1885). Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M,N. H. ser. 5, vol. xvii. pp. 40-53 (1886). Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M. N. H. ser. 5, vol. xvii. pp. 112-127 (1886). Descriptions of Sponges from the neighbourhood of Port Phillip Heads, South Australia. Ann. M. N. 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Ueber Lithistiden aus Japan. Ber. Vers. Nat. pp. 110-112 (1884). Faunistische Studien in Japan, Enoshima, und die Sagami-Bai. Arch. f, Nat. (2) xlix. p. 102 (1884). 344. Donati, V. Della storia naturale marina dell’ Adriatico. Venezia (1750). 1886.] POSITION AND CLASSIFICATION OF SPONGES. 607 345. D’Orbigny, A. Prodréme de Paléontologie stratigraphique universelle des animaux mollusques et rayonnés. (1849-1850.) Compare Orsicyy, no. 1121-i123. 346. ——. Cours élémentaire de Paléontologie et de Géologie stratigraphique. (1849-1852.) Compare Orsreny, no. 1124-1126, 347. Duchassaing, P., et G. Michelotti. Spongiaires de la Mer Caraibe. Haarlem (1864). 348. . Revue des Zoophytes et des Spongiaires des Antilles. Paris (1870). 349. Dufour, T. Notice sur un champignon parasit des Eponges. Bull. Soc. Vaudoise Se. Nat. vol. xviii. p. 144 (1882). 350. Dujardin, F._ Observations sur les Eponges et en particulier sur la Spongille ou Eponge d'eau douce. Ann. Sci. Nat. sér. 2, tom. x. pp. 5- 13 (1838). 351. ——. Observations sur les Eponges. C. R. tom. vi. p. 676 (1838). 852. ——. Observations sur les Eponges. L’ Institut, tom. vi. no. 229, p. 157 (1838). [853.] ——. Observations sur les Eponges. Soc. Philom. Extr. Proc.-verb. p- 81 (1838). 354. ——. Histoire naturelle des Zouphytes Infusoires, pp. 305,306. Paris (1841-1842). 355. Duncan, P. Martin. On some Spheroidal Lithistid Spongida from the Upper Silurian Formation of New Brunswick. Ann, M. N. H ser. 5, vol. iv. pp. 84-92 (1879). 356. . On a Parasitic Sponge of the Order Calcarea (Mobiusispongia parasitica). J. R. Micr. Soc. vol. iii. pp. 877-383 (1880). 357. On some Remarkable Enlargements of the Axial Canals of Sponge- Spicules, and their Causes, J. R. Micr. Soc. ser. 2, vol. i. pp. 557-872 (1881). 358. ——. On a Lithistid Sponge, and on a form of «0.7. ssveiccte'y sides Waceccteces ccevusesssca’ 96 4. Preliminary Notice of the Isopoda collected during the Voyage of H.M.S. ‘Challenger.’— Part III. By Fravyg E. Bepparp, M.A., F.R.S.E., F.Z.S., Prosector to the Society.. 97 5. On a Variety of Anthocharis eupheno, from Mogador. By J. H. Lexcn, F.ZS. ........ 122 6. On a ay Species of Bird of the Genus Copsychus. By R. G. Warviaw Rawaay, F.Z.S., Pareto fatten! eft royal cinreleta:eve\sTals’s- 218 XXIL cir Hybria Grouse between Lagopus albus and Tetrao tetrix ...... 224 XXIII. Ctenosaura erythromelas...........cseceeeeresteceneetces . 241 XXIV. Rana arvalis........ .... Wahdln:0.6 gia8, ein Bio's ounte sic leinis piacotgs ccee 242 ae } Balanoptera borealis Re EiBee ealasaledaiefaisiatoieia’ whelsie ioichereN rate ain oles earns TES ieee Wes 1 a ee ‘NOTICE. According to present arrangements the ‘ Proceedings’ are issued in four parts, as follows :— Part I. containing papers read in January and February, on June Ist. 3 e % » March and April, on August Ist. Iii. es a », May and June, on October Ist. IV. 4 “7 »» November and December, on April Ist. — The price is 12s. per part for the edition with coloured, and 3s. per part for that with uncoloured Plates. 205 a PROCEEDINGS OF THE SCIENTIFIC MEETINGS OF THE ZOOLOGICAL SOCIETY ‘OF LONDON, FOR THE YEAR 1886. PART TE, CONTAINING PAPERS READ IN BS - apes OCTOB. , 1886. PRINTED FOR THE SOCIETY, | SOLD AT THEIR HOUSE IN HANOVER SQUARE. | LONDON: . MESSRS. LONGMANS, GREEN, AND CO, PATERNOSTER-ROW. | yy a Si [Price Twelve Shillings.] LIST OF CONTENTS. PART III.—1886. May 4, 1886. é Page The Secretary. Report on the Additions to the Society’s Menagerie in April 1886 ........ 266 Mr. E. L. Layard. Exhibition of a rare Beetle, and of a series of Shells of the genus Bulimus 267 Mr. F. W. Styan, F.Z.S. Letter from, respecting some Chinese animals ......- siecle oOdl 1. Remarks on four rare Species of Moths of the Family Sphingide. By W. F. Kirsy, Assis- tant in Zoological Department, British Museum (S. Kensington), (Plate XXVII.).. 269 2. Observations on the Ovarian Ovum of Lepidosiren (Protopterus). By Franx E. Bepparp, M.A., F.RB.S.E., Prosector to the Society. (Plates XXVIII. & XXIX.) ............ 272 3. On the Mode of Attachment of the Ovum of Osmerus eperlanus. By J. T. CunnincHam, B.A., E.R.S.E., Fellow of University College, Oxford, and Superintendent of the Scot- tish Marine Station. (Communicated by Mr. F.E. Bepparp.) (Plate XXX.) .... 292 May 18, 1886. Mr. C. W. Rosset. Exhibition of Photographs taken in the Maldive Islands, and remarks on his Zoological Collections ..........-.-++ Aer aoc akg Te Mr. Philip Crowley, F.Z.S. Exhibition of some Pupz of Nocturnal Lepidoptera from Natal AP oot eoreetes ry 5 eee ee ee ee Mr. Joseph Whitaker, F.Z.S. Exhibition of a specimen of Wilson's Phalarope shot in England «...+-.....- o stuicig/S'siala(wicomne eisinid!siwinleisioisinjee sajsiain Vive ce cssece eeseeeee 1. Ona fourth Male Specimen of King William the Third’s Paradise-bird. By A. B. Meyer, M.D., Director Royal Zoological Museum of Dresden, C.M.ZS., Ke. ..-+-...-+0++ . 297 2. Descriptions of some new or little-known Earthworms, together with an Account of the Variations in Structure exhibited by Perionyx excavatus, E.P. By Frank E. Bepparp, M,A., F.R.S.E., Prosector to the Society «....+.0..-seeeeseeeee emaels co 2OR 3. Remarks on the various Species of Wild Goats. By P. L. Scuater, M.A., Ph.D., F.BS., Secretary to the Society. (Plates XXXI. & XXXII) ............. anes: oasis Olaam June 1, 1886. The Secretary. Report on the Additions to the Society's Menagerie in May 1886 ........ 318 Dr. Giinther, F.R.S. Exhibition of a specimen of a small Fish of the genus Fierasfer im- bedded in a Pearl-Oyster.....0.scecececsccccceeseces esinwia's a i iii Contents continued on page 3 of wrapper. i ¢ ; Contents (continued). Page Mr. Sclater. Remarks on interesting animals observed during a visit to the Zoological Gar- dens of Rotterdam, Amsterdam, Cologne, Antwerp, and Ghent..........ee....0--5 ¢ 320 Mr. J. M. Cornély, C.M.Z.S. ae from, respecting the breeding of Michie’s Deer in his Menagerie .........-0e4- Mt Seerats atthe ojetatsiwialarare e+ ai-s'efein/hiefola, Arejare 4 iwa ona @u'eisls en a's 320 1. Notes on the Convoluted Trachea of a Curassow (Nothocrax urumutum), and on the Syrinx in certain Storks. By Frank E. Bepparp, M.A., F.R.S.E., Prosector to the Society «+........+005- ey OPE er or Cee Medan ou meine eG a aptamer 2. On a small Collection of Dragonflies from Murree and Campbellpore (N.W. India), received from Major J. W. Yerbury, R.A. By W. F. Kirsy, Assistant in Zoological Department, British Museum. (Plate XXXTIT.) ........ cess ee ceeeee nese ee ens 3 June 29, 1886. The Secretary. Exhibition, on behalf of Mr. J. Brazier, C.M.Z.S., of a series of 55 eggs laid by a Pacific Porphyrio -.............. Sb POE: SOD OOIOn CODC: DUOO err. 330 Capt. J. A. M. Vipan, F.Z.S. Letter from, on the mode of Nesting of a South-American Siluroid Fish (COO Tatlig/ s-UCCOT AUS) ajninie)cisicis 05010. 6 .ujs)e's.a'e vac osie e cieis'eins pieenn dine 330 1. General Observations on the Fauna of Diego Garcia, Chagos Group. By Gixperr C. IBOURWE, W.A., Now Colleze, Oxford. _ Lond., Fell. Madras Univ., Professor of Biology in the Presidency College, Madras. ow (Communicated by Prof. Ray Lanxester, F.Z.8.) 0.0 ..0c cece cece cece ee en ee tees 662 _ Appendix : List of Additions to the Society’s Menagerie during the Year 1886.......... «. 673 ‘Index. RROTAV SIAC ctereye isis =) 2s Ot ORE II ee oem Laer up athintas hc ease ee 699 LIST OF PLATES. 1886. PASE FV, Plate Page - XL. | New Indian Lepidopt 42} XL f ndian Lepidoptera ......-++++++++eeeeeeerereeerses XLIT. Sue Anatomy of Geococcyx californianus ...........+... wweer 466 XL: XLVI. Scelidotherium leptocephalum ....-+++++-+.+seeeceeeeeee ) XLVIT. Scelidotherium bravardi) ......6....00cce se cece ceseeee | XLVIIT. Scelidotherium’chilense ...... 6... .dej-eeeecceceee cece . f 491 XLIX. Fig. 1. Scelidotherium bravardi. Fig.2. S.chilense. Fig. 3. 8. leptocephalum. Fig. 4. ? 8. bravardi........++..-- ) L. Fig.1. Bombinator bombinus. Fig. 2. B. igneus.......+- -.. 499 DI. Gazella maso 2. is. b. ese cee tenes cee e seen sees creet nse 504 Lil. cee LITT. } Structure of Ovum in*the Dipnoi ....... aie ai wan bY Minhas oferore -.. 505 LIV. : e : LV. Squaloraja-..... hg TOE Le eevee See) Saree + 527 Ha --s Conunuserubriorguis cate