THE PEOOEEDINGS OF THE LINNEAN SOCIETY OF N EW SOUTH WALES. VOL. IX. WITH SEVEN"TY-01TE PLATES- FOR THE YEAR 1884. SYDNEY: PRINTED AND PUBLISHED FOR THE SOCIETY BY F. CUNNINGHAME & CO., UG PITT STREET, AND SOLD BY THE SOCIETY. 1885. CONTENTS OF VOL. IX. PART I. PAGE Supplement to the Descriptive Catalogue of the Fishes of Australia. By William Macleay, F.L.S., &c 2 On some Batrachians from Queensland. By Charles W. De Vis, M.A. 65 Occasional Notes on Plants Indigenous in the immediate neighbour- hood of Sydney. No. 6. By E. Haviland 67 Studies of the Elasmobranch Skeleton (Plates 1 and 2). By. William A. Haswell, M.A., B.Sc 71 A Monograph of the Australian Sponges. By B. von Lendenfeld, Ph.D. Parti 121 The Scyphomedush in the total length. 3rd and 4th dorsal spines l£ in the height of the body. Like A. coaspersus, but distinguished by the remarkable length of the caudal peduncle which is only a little shorter than the head. The number of rays also in the transverse line is smaller, and the 8th dorsal spine is sometime absent ; the suprascapula is toothed, the anal fin has ten rays at least, that of A. conspersus only 9. Colour , on the trunk numerous black spots or specks arranged longitudinally along nearly the whole length of the side ; beneath this line each scale has a black spot, but not arranged in lines : the first dorsal has the membrane dark, especially towards the summit Ventral fins the same ; the other fins light. Caudal slightly rounded. 13 ctm. 10 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, King George's Sound. (Klunzinger.) 1143. Apogon Lemprieri. Johnston. Proc. Roy. Soc. Tasmania 1882, p. 142. " B. 7. D. 6. 1/10. A. 2/9. L. lat. 27. L. far. 3/10." " The height of the body is equal to the length of the head, and is contained nearly three times in the total length. Snout short ; length about half the diameter of the eye, which latter is fully one-third of the length of the head. The maxillary scarcely reaches the vertical from the posterior margin of the eye. Lower jaws prominent. Two minute cavities on upper part of snout. Hinder margin of prseoperculum minutely dentate, anterior ridge simple. Spine of operculum reduced to a soft pointed membrane. No dark spots on root of caudal. Uniformly brownish, with iridescent shades of purple, gold, and light blue ; lighter towards belly. Tips of ventral and dorsal fins blackish. Other fins light reddish." Hah. Dunkley's Point, Sandy Bay, Tasmania. One specimen 4 inches long. Species 86. Nannoperca Riverince. Macleay. Klunzinger's Paradules foetus seems to be this species. His genus Paradules must go, as Gunther's genus Nannoperca has priority by more than 10 years. 1144. Nannoperca obscura. Klunz. Paradules obscurus Klunz. Archiv. f. Naturg., 1872. Sitzb. der K. Akad. der Wissensch., 1879, tab. 1, fig 2. D. 9/10. A. 3/6. P. 9-10. C. 17. L. lat. 28-30. L. tr. 21/10. Height 3| and head 3g in the length. Body elongate, elliptic ; profile of head slightly parabolic, nearly straight. Head, snout, forehead and prseorbital naked ; mouth small, the maxillary reaching only to below the front margin of the eye. Praeorbital nearly scpiare, dentate on the posterior mai'gin and angle. Operculum with two spines. Lateral line not continuous, following the line of the back. Dorsal fin deeply notched, the first spine small, the last ray longest ; the fin commences before BY WILLIAM MACLEAY, F.L.S., &C. 11 the last third of the pectoral ; the third anal spine is higher than the second, the soft dorsal and anal fins are alike , the ventrals commence beneath the first quarter of the pectorals and extend to the anus. Caudal slightly rounded. Colour in spirit dark brown, fins grey. Yarra Lagoon. (Klunzinger.) 1145. Microperca Tasmania. Johnston. Proc. Hoy. Soc. Tasmania, 1882. p. 110. D. 8/7V A. 3/8. L. lat. 28-30. L. tr. 12. P. 13. " Body compressed. Length of head equal to depth of body at shoulder, and contained in total length four times. Prceoperculum not serrated. Scales relatively large, ctenoid. Eye large, nearly as broad as length of snout ; the latter contained in head four times; dorsal deeply cleft, the first spine slightly pointing forward when erect ; situated immediately over the posterior extremity of pectoral ; the second and third spines longest. Anal commencing in a vertical line, scarcely in advance of the first spinous ray of second dorsal. The second dorsal and the anal soft rays gradually increase in width, the last two or three being of equal length and nearly half the length of the body. Catidal peduncle somewhat elongate. Caudal truncate. Colour dark olive with a pinkish streak along the sides from shoulder to tail. Base of dorsal, anal and caudal tins pinkish, with blackish margins. Belly silvery tinged with gold. Eye dark blue, with golden streak around eye ball." Abundant in Rivers North and South Esk. (Johnston.) Length, 3 to 5 \ inches. 1146. Gulliveria Ramsayi. N. sp. B. 5. D. 6/£. A. 2/9. L. lat. 44. L. tr. 4/12. Body compressed and moderately elevated ; the height being twice and two-thirds in the length, exclusive of the caudal fin ; the length of the head is about the same ; the diameter of the eye is rather more than the width of the interorbital space, which is flat, naked, much channelled, and about equal to the length of the snout measured to the extremity of the lower jaw. The 12 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, profile of the head is slighlv concave, but swells out towards the snout into a rather prominent convexity truncate in front. The cleft of the mouth is slightly oblique, the lower jaw distinctly longer than the upper, the maxillary large, triangular, naked and extending to, or very nearly to, the vertical from the posterior margin of the eye. The teeth in the jaws are numerous in broad viliform bands, those on the vomer are situated on a very prominent horse-shoe shaped bony protuberance. The prseoper- culum has a double ridge, both quite smooth ; the operculum has one membranous point. The dorsal spines are very strong, the first very short, the last less than half the length of the second ; the first anal spine is very short : the caudal fin is rounded. The lateral line follows the curve of the back. Colour (in spirits) pale brown, the membranes connecting the spines of the first dorsal fin, and the rays of the pectorals, black. Length 5 inches. From fresh water inland from Port Darwin. Species 114. Oligorus Macquariensis. This fish is found in the Mary River, Queensland. 1147. Oligorus Coliath. De Yis. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 318. Moreton Bay. 1148. HOMALOGRYSTES LUCTUOSUS. De Vis. Pro. Linn. Soc, K S. Wales, Vol. VII., p. 369. Brisbane. 1149. Therapon Mac leay anus. Ramsay. Proc. Linn. Soc. N. S. Wales, Vol. VI., p. S31. Macquarie River. Species 139. Therapon niger. Casteln. Klunzinger thinks this fish is identical with Therapon ellipticus of Richardson. It should be noted, however, that their respective habitats are far removed from one another; the one inhabiting the rivers of the Murray system, the other those of Western Australia. BY WILLIAM MACLEAY, F.L.S., &C. 13 1150. Therapox fuliginosus. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 201. Burdekin River. 1151. Therapon parviceps. Macleay. Proc. Linn. Soc. N. S. Wales. Vol. VIII., p. 201. Burdekin River. 1152. Diagramma punctatum. Cuv. and Val. Gunth. Cat. 1 p. 323. Quoy and Gaim. Voy. Astrol., p. G99., PI. 12, fig. 2. Plectorhynchus pictus. Bleek. Alt. Ichth. Perc. 11, p. 24, tab. 51, fig. 4. Syn. Diagramma ocellatum, cinerascens, centtcrio, pcecilopterum, and balteatum. Cuv. and Val. B. 7. D. 10/22-23. A. 3/7. L. lat. 85. Vert. 12/15. " The height of the body is 3£ in the total length, the length of the head 4*. The width of the eye is scarcely longer than the extent of the snout, and 3 J in the length of the head. The upper maxillary extends to the vertical from the front margin of the orbit. Prseoperculum with the posterior limb vertical, and the angle rounded, finely and equally serrated. The dorsal fin moves in a high scaly sheath, and is even or slightly notched ; the spines are moderate, the second and third the longest, half the length of the head. Caudal truncated ; the second and third anal spines equally strong, the latter rather longer. Body and vertical fins with numerous brown spots, disappearing with age ; the dorsal and anal fins with a black mai'gin. Sometimes light longitudinal streaks at the side of the head." Queensland. (Klunzinger.) 1153. Diagramma labiosum. Macleay. Proc. Linn. Soc. N. S. Wales. Vol. VIIL, p. 202. Wide Bay. Species 157. Histiopterus labiosus. Add Port Jackson to the other "habitats." 1154. Scolopsis affinis. Peter. Monatsber. Berlin Akad., 1876, p. 832. Klunz. Sitzb. der K. Akad. der Wissensch, 1879. D. 10/9. A. 3/6-7. L. lat. 45. L. tr. 4J/12. 14 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Height of body and length of head 4 times in the total length. Body oblong ; the spine of the prfeorbital not very distinct, as in S. inermis, Richards. Eye large. Colour dark, underneath the dorsal fin a darker longitudinal band. A horizontal silvery stripe on the prseorbital. 8 ctm. Port Darwin. (Klunzinger.) 1155. Scolopsis specularis. De Vis. Proc. Linn. Soc. N. S. Wales. Vol. VII., p. 369. Queensland. 1156. Synagris upeneoides. Bleek. Gunth. Cat. 1 p. 375. Dentex upeneoides. Bleek. Atl. Ichth. Perc. 11, p. 92. tab. 49, fig. 2. B. 6. D. 10/9. A. 3/7. L. lat. 50. " The height of the body is 4| times in the total length, the length of the head 4£ ; the diameter of the eye is one-third of the latter and as long as the snout. The upper maxillary reaches to the vertical from the anterior margin of the orbit ; the height of the prseorbital is I5 in the diameter of the eye ; there are three series of scales between the prceorbital and the margin of the prgeoperculum. Six canine teeth in the upper jaw, none in the lower. The spines of the fins slender, flexible ; the middle ones of the dorsal longest, half the height of the body ; the soft portion of the fin lower than the spinous. Caudal deeply forked. Rose- coloured ; the soft dorsal with a yellow longitudinal band near the upper margin." (Bleek.) Queensland. (Klunzinger.,) Family. SQUAMIPINNES. 1157. Chelmo Mulleri. Klunz. Sitzb. der. K. Akad. der Wissensch., 1879, p. 361. D. 9/29-30. A. 3/21. L. lat. 50. L. tr. 9/25 (in front 10/22.) Height of body 2 and length of head ?>\ in the total length. Snout very short, but narrow and tubular, it is 2£ in the length of the head. The prseorbital and prseoperculum are toothed on the posterior margin ; caudal truncate. BY WILLIAM MACLEAY, F.L.S., &C. 15 The colour is the same as that of C. rostrahis, but the bands are a little broader, and of an uniform brown colour without white margin. The ventral fins are black. (Klunzinger.) No habitat is given of this species by Dr. Klunzinger, but he includes it among his Australian Fishes. Family. SPARINE. 1158. GlRELLA CARBONARIA. De Vis. Proc. Linn. Soc, N. S. Wales. Vol. 8, p. 283. Moreton Bay. Black Bream of the Brisbane Market. 1159. GlRELLA MENTALIS. De Vis. Proc. Linn. Soc, N. S. Wales. Yol. 8, p. 284. Moreton Bay. Genus Pemilepterus. In both jaws a single anterior series of cutting teeth, implanted by a horizontal posterior process, behind which is a band of villiform teeth; fine teeth on the vomer, the palatine bones and the tongue. The soft portions of the vertical fins thickly enveloped by minute scales ; eleven doi'sal and three anal spines. Prseoperculum generally denticulated. Scales of moderate size, bony. Seven branchiostegals. Pyloric appendages sometimes in small number, sometimes exceedingly numerous. Air bladder notched posteriorly, and sometimes anteriorly. Tropical seas. 1160. Pemilepterus indicus. Cuv. and Yal. Klunz. Sitzb. der K. Akad. der Wissensch., 1879. Plate 7. P. tahmel Klunz. Fisch. Both. Meer. 1, p. 795 (nee. Forsk.) D. 11/11-12. A. 3/11. L. lat. G6. L. tr. 10-11/20-22. This species differs from P. tahmel Forsk. in the 2nd dorsal, being not nearly so high, and always lower than the middle highest dorsal spines. It is also lower than the anterior highest anal rays, which are not quite as high as the highest dorsal spines. In these respects this species resembles P. Waigiensis and P. lembus, but these again have always a greater number of dorsal 16 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, rays. The height of the body is 2f, the length of the head 5, in the total length ; the fifth dorsal spine 3, the highest dorsal ray 4, in the height of the body. The prseorbital is naked, in P. Waigiensis it is scaled. 30 Ctm. King George's Sound. (Klunzinger.) Species 230. Pachymitopon squamosum. All. and Macleay. Dr. Klunzinger suggests that this may be the Pemilepterus tahtnel of Forsk. 1161. Haplodactylus jkeandratus. Sol. Richards Trans. Zool. Soc. III., p. 83. Klunz. Archiv. fur Naturg. XXXVIIL, 1872, p. About 18 inches in length, of a brownish olive colour, with anastomosed wavy lines, and small white spots, getting gradually lighter towards, and quite white on the belly. Teeth, numerous in the jaws, in many rows, lanceolate, compressed, rather obtuse, flexile ; a few acute ones on the palate, none on the tongue. Pectoral fins ovate, obtuse, short, not reaching to half the length of the abdomen, unarmed, at the base externally rivulose, ashen coloured, immaculate, with 14 rays, the inferior rays covered with a thick skin. Anal fin broadly rivulose, acute, 7 rayed, the first ray simple, the last bipartite. Caudal fin blackish-olive, clouded with paler. B. 6. D. 16/18. P. 14. A. 1/6. C. 17. The above is a translation of Dr. Solander's description, who took it at Cape Kidnapper, New Zealand. Sir John Richardson adds, the head is scarcely gibbous over the orbit, the spinous dorsal is higher than the jointed one, and the caudal is truncated with the corners rounded. Re-described at great length by Dr. Klunzinger (loc. cit.) Hobson's Bay. (Klunzinger.) 1162. Lethrinus nebulosus. Forsk. Gunth. Cat. 1, p. 460. Syn. L. esculentus. Cuv. and Val. D. 10/9. A. 3/8. L. lat. 48. L. tr. 6/15. The height of the body is 3| in the total length, the length of the head four times. The snout is rather elongate and pointed. BY WILLIAM MACLEAT, F.L.S., &C. 17 The length of the diameter of the eyes is rather more than the width of the distance between them, and 1| in the length of the snout ; the maxillary reaches to the vertical from the anterior nostril. There is a slight protuberance before the upper anterior angle of the orbit. Canine and molar teeth moderate. Dorsal spines moderate ; the fourth rather shorter than the longest ra y, and one-third of the length of the head ; caudal forked with pointed lobes. Olive, bluish spots on the sides of the head. (Gunther.) Port Darwin. (Klunzinger.) 1163. Lethrinus reticl'latls. Cuv. and Val. Gunth. Cat 1, page 457. D. 10 9. A. 3/8. L. Lat. 43 (48 ?) L. tr. 5 17. The height of the body is 4 in the total length, the length of the head 3| ; the snoirt is pointed, scarcely longer than the diameter of the eye, which is one-third of the length of the head, the maxillary reaches nearly to the vertical from the anterior margin of the eye. Canine teeth distinct and curved ■ lateral teeth conical, the posterior ones obtuse. Caudal fin emarginate with pointed lobes. Olive or rose coloured ; head and body with violet specks, arranged in irregulai transverse bands ; generally two violet streaks from the eye to the snout ; the spinous dorsal marbled with violet ; ventral fins violet ; the rays of the vertical fins with five cross streaks. Endeavour River and Port Darwin (Klunzinger.) Family. CIRRFHT1D.K. Species 27*2. Chilodactylus spectabilis. Hutton. Add to synonyms Chilodactylus asper Klunzinger. Archiv. fur. Naturg. XXXVIII., 1872. Mr. Ft, M. Johnston (Cat. Roy. Soc , Tasm., 1883) considers C. Alport i. a distinct species. In my catalogue I followed Dr. Gunther. 11G4. Chilodactylus xebulosus. Klunz. Archiv. fur. Xaturg. XXXVIIL, 1872. Sitzb. der K. Akad. der Wissensch., 1879, p. 364. D. 16,24. A. 3/9. P. 8,6. L. lat. 55. L. tr. 5/12. 0 18 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Height of body 3-| in the total length. Body elliptic ; profile of head slightly parabolic ; a narrow band of small canine teeth in both jaws ; the maxillary readier to below the anterior margin of the eye. Scales of head small ; forehead without process ; scales of body slightly rough ; lateral line nearly quite straight, its figures form simple obliquely ascending stride. Dorsal spines rather low, not higher than the rays ; those of the anal a little higher than those of the dorsal ; the anal is rather obliquely truncated. The second simple pectoral ray is the longest, but only one- sixth longer than the longest compound one, and reaches to the extremity of the ventrals, which commence under the middle of the pectorals, and do not reach the anus. Caudal fin deeply emarginate, the outer rays being half again as long as the middle ones. Colour ; yellowish with dark nebulose transverse bands, 8-9 in number, which commence broad on the back and extend obliquely forwards, the 3rd, 4th and 5th arch shaped or angular forwards, forming each a longitudinal somewhat continuous stripe. The uppermost runs close along the eye, the second over the pectoral to the lower margin of the eye, the third rather indistinct extends along the belly. The dorsal and caudal fins are nebulous or spotted ; mai-gins of all the fins except the pectorals white ; ventrals and anal dark. 16 Ctm, Queenscliff. Port Phillip. (Klunzinger.) 11G5. Chilodactylus Mulhalli. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 366. Port Jackson. Genus Dactylophora. De Vis. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 284. 1166. Dactylophora semimaculata. De Vis. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 284. South Australia. Genus Psilocranium. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII. , p. 439. BY WILLIAM MACLEAY, F.L.S., &C. 19 1167. Psilocranium Coxn. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 440. PI. XXII Port Jackson. Genus Mendosoma. Gay. One dorsal fin deeply. notched with twenty-two (23) spines; the anal fin of moderate length, the caudal forked ; the simple pectoral rays feeble, not exceeding the margin of the fin. Small teeth in the upper jaw only, none in the lower or on the palate. Scales of moderate size ; cheeks scaly. Six branchiostegals. 1168. Mendosoma allporti. Johnston. Proc. Roy. Soc, Tasm., 1880, p. 64. B. 6. D. 23/1.. A 3/18 P 16 L lat 76# L tr 5//16> "Body elliptical, compressed. Head small, pointed. Cheeks scaly. Height of body is 3^ in the total length ; the length of the head five times. Dorsal fin notched ; the sixth, seventh and eighth spines are the longest, higher than the longest of the soft dorsal, and about one-fourth the depth of the body. The first soft dorsal is situated in a line vertically drawn through the anus ; the third anal spine is longer than the thickish second, and about half the length of the longest dorsal spines. Pectoral rays more or less covered with linear oblong scales, simple rays fine, feeble, all shorter than the immediately superior branched rays. Body scales moderately large anteriorly, decreasing hi size towards the tail. Caudal forked. Uniformly blackish grey, with a deeper shade along the back." (Johnston.) Tasmania. Family. SCORPyENID^. Species 299 Holoxenus cidaneus. Gunth. Mr. Johnston (Proc. Roy. Soc. Tasm., 1882, p. 114), describes a fish, known in Tasmania as the Velvet Fish, which he believes to be H. cutaneus of Gunther, but he finds some difference in the fin formation. Should it turn out to be a distinct species, he proposes for it the name Holoxenus Guntlteri. 20 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Family. TEUTHIDID^E. 1169. Teuthis sutor. Cuv. and Val. Gunth. Cat. III., p. 317. The height of the body is more than one-third of the total length. Brown, minutely dotted all over with whitish. (Val.) Klunzinger got this species from Port Darwin, and gives a full description of it in " Sitzb. der K. Akad. Wissensch., 1879, p. 393." 1170. Teuthis fuscescens. Houtt. Gunth. Cat. III. p. 321. Schleg. Faun. Japon. Poiss., p. 127, pi. 68, f. 1. The height of the body is contained three times and a half in the total length. Caudal fin scarcely emarginate. Uniform brownish. Queensland. (Klunzinger.) Family. BERYCIELE. 1171. Trachichthys Macleayi. Johnston. Proc. Roy. Soc, Tasmania, 1880. D. 5/13. A. 3/10. V. 8. " Scales minutely irregularly spiniferous ; a series forming the pierced scales of the lateral line (about fifty) larger, and armed with one or two visibly prominent transparent spines. Height of body 2£ in the total length, the length of the head nearly three times. Cleft of the mouth wide, almost vertical. The serrated ventral keel is composed of 13 prominent spiniferous scutes. Upper and lower margins of caudal peduncle armed respectively with 8 and 7 strong adpressed translucent spines. Colour of a uniform bright golden yellow when fresh." Length, 9 A inches. Mouth of the Der went River. Genus. Cleidopus. De Vis. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 367. 1172. Cleidopus gloria maris. De Vis. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 368. Brisbane River. BY WILLIAM MACLEAY, F.L.S., &C. 21 1173. Beryx Mulleri. Klunz. Sitzb. der K. Akad. der Wissensch., 1879, p. 359, tab. 3, fig. 1. B. 8. D. 7/14. A. 4/14. V. 1/7. P. 2/13. L. lat. 47. L. tr. 5|. 1/12 to 6|-7. 1/12. Height of body 3g and length of head i\ in the total length. It differs from B. affirm in the scales of the lateral line being more numerous as also the rays of the dorsal and anal tins. In most other particulars it is very like B. affinis. The projecting chin has in front on each side an obtuse spine and above it a pore. The caudal fin is long and deeply forked, the fork tips narrow, pointed, and of the same length. Lateral line straight. Colour reddish with a blue glimmer (in spirits), especially on the upper part. 25 Ctm. King George's Sound. (Klunzinger.) Family. KURTIDiE. Klunzinger describes two species Pempheris Mulleri and Pem- pheris multira/rdiatus both from King George's Sound. I cannot make them out to be different from those already described. Family POLYNEMID^. 1174. Polynemus specularis. De Vis. Proc. Linn. Soc. N. S. Wales. Vol. VIIL, p. 285. Brisbane River. 1175. Polynemus tetradactylus. Shaw. Gunth. Cat. 1 p. 329. Macl. Proc. Linn. Soc, N. S. Wales, Vol. VIIL, p. 203. D. 8/13i15. A. 2/16-17. L lat. 73-85. Four pectoral appendages, not or scarcely reaching beyond the tip of the ventral fin. Pyloric appendages in immense number. Hab. Mouth of the Burdekin River. 1176. Polynemus Sheridan i. n. sp. D. 7/3. A. 2/11. L lat. 62. Oblong, compressed. Height of body one-fourth of the length exclusive of caudal fin ; length of head slightly more. Eye large, lateral, near the snout, with a broad depressed interorbital space, 22 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, showing a slightly concave profile ; two nostrils close together in front of the upper part of the orbit ; snout roundly pointed, con- siderably overlapping the mouth ; maxillary large and triangular, appearing first under the hinder margin of the eye and extending far behind it. Preeoperculum serrated on the posterior limb, and without a spine near the angle. Five pectoral appendages, the two upper ones extending far beyond the tips of the ventrals. The first dorsal fin is vertically in advance of the root of the ventrals ; the fh-st spine is very strong, and equal in height to f the length of the head, the second is a little higher, the others become gradually lower ; all are feeble except the first, and none of them are filamentose. The distance between the dorsals is more than the length of the base of the first; the second has a falcate appearance like the anal, and both are scaly and fleshy. The caudal fin is long, forked, scaly, and slightly filamentose. The distance between the origin of the ventrals and that of the anal, exactly equals the length of the head. The scales are of moderate size, resembling somewhat those of the Mullet (Mugil), the lateral line is straight. The coloration is bluish-silvery towards the back, and whitish towards the belly ; the dorsal, anal and caudal fins are blackish ; the pectorals, ventrals, and pectoral appendages whitish ; each line of scales shows a more or less distinct longitudinal streak. Length, 26 inches. Mary River, Queensland. I am indebted to the Hon. B. Sheridan for the specimen of this fish here described. It is abundant at some seasons in the tidal waters of the Mary, and has been known to attain a weight of 100 lbs. It is highly valued as a food-fish. Family. SCI^ENID^E. Genus Umbrina. Cuv. Body oblong ; muzzle convex, with the upper jaw overlapping the lower; a short barbel under the mandibulary symphysis. Two dorsals, the first with nine or ten flexible spines ; the anal fin BY WILLIAM MACLEAY, F.L.S., &C. 23 with one or two ; scales moderate ; pseudobranchise. The air bladder with or without appendages or absent. Pyloric cceca in small number. All Seas and Mouths of Rivers. 1177. Umbrina Mulleri. Klunz. Sitzb. der K. Akad. tier Wissensch., 1879. D. lO/^. A. 2/7. L. hit, supra. 63 infra. 55. L. tr. 6/16. Height of body 4 and length of head 4J in the total length. Like U. Russellii and Dussumieri, but with a shorter barbel on the chin and a different fin formula. The snout is round and projecting. The barbel is very short not 1/3 of the diameter of the eye, with a pore at its base and ai'ound it four others ; there are also several pores on the snout ; prajoperculum rounded without hard teeth. Teeth villiform in rows, some a little larger on the outer row of maxillaries ; 2nd and 3rd dorsal rays nearly equal, flexible ; 2nd anal ray much larger than the 1st. The maxillary reaches to behind the middle of the eye ; the posterior rays of the dorsal a little shorter than the others, and still shorter than those of the anal. The caudal fin is obtusely rhombic. Colour above, dark, on the ventral side silvery ; on the ventral side of the head, and snout and cheeks this colour is sharply circumscribed so that only the lower margin of the praeorbital is silvery. All the fins are dark, the dorsal especially, the membranes densely speckled. 20 Ctm. Queensland. (Klunzinger. ) 1178. CORVINA AUSTKALIS. Grlinth. Rep. Shore Fishes. Voy. Challenger. Part 6, p. 33. Corvina argentea. Macl. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 204. Mouth of Burdekin and Mary Rivers. Queensland. 1179. Corvina miles. Cuv. and Val. Gunth. Cat. 2 p. 300. D. 9-10/^.30. A. 2/7. The height of the body is nearly equal to the length of the head, and one-fourth of the total ; the diameter of the eye equals the 24 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, length of the snout, and is one-fourth of the length of the head. The upper jaw overlapping the lowei*. The band of maxillary teeth with an outer row of stronger ones. The second anal spine very strong and as long as the first ray ; caudal pointed. Above greyish green, sides and belly silvery ; dorsals minutely dotted with brown, and with a black upper margin, in front of each dorsal ray a small brownish spot ; ventrals whitish ; the other fins with a blackish margin. Queensland. (Klunzinger.) Sdcena Mulleri Steind, is probably one of the ScirenicUe already mentioned, but I cannot find any description of it. Family. CARANGID^. 1180. Caranx ignobilis. Forsk. Caranx sansun. Rupp. Gunth. Cat. 2, p. 4-47. D. 8/19V A. 2W]17. L. lat. 30. The teeth of the upper jaw form a villiform band, with an outer series of stronger ones ; those of the lower one in a single series. The height of the body is 3 to 3 \ in the total length. Breast scaly ; the lateral line is bent anteriorly, the width of the arch being equal or nearly equal, to the length of the straight portion ; the latter begins in the vertical from the seventh dorsal ray. The plates are very well developed and distinct from the beginning of the straight portion. The lower jaw is longer than the upper, and the maxillary reaches bejond the vertical from the centre of the eye. Opercular spot none. Port Darwin and Cleveland Bay. (Klunzinger.) 1181. Caranx compressus. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VIII, p. 204. Lower Burdekin, salt water. 1182. Chorinemus Sancti-Petri. Cuv. and Val. Gunth. Cat. 2, p. 473. D. 7/20l21. A. 2/18V Vert. 10/16. The height of the body is nearly equal to the length of the head, and one-fifth of the total. The maxillary is triangular and BY WILLIAM MACLEAY, F.L.S., &C. 25 flat posteriorly, and reaches beyond the vertical from the centre of the eye. The length of the intermaxillary is contained one and two-third times, or twice in that of the head. The snout, in mature fishes, is nearly twice as long as the diameter of the eye. A series of rounded indistinct blackish spots above the lateral line, sometimes a second j-ow beneath, sometimes both absent. An indistinct blackish streak from above the eye to the shoulder. Top of the dorsal black. Fort Jackson (Macleay), Port Denison (Klunzinger.) 1183. Equula splexdens. Cuv. and Val. Gunth. Cat. 2, p. 501. Kner Novara reise, p. 163. D. 8/15. A. 3/14. Yert. 10/14. The height of the body is 2\ to 2| in the total length, the length of the head four times. The upper profile is much more convex than the lower, A pair of small spines above the anterior margin of the orbit ; the cavity on the head is about twice as long as broad. The lower prteopercular margin is finely serrated, and its length is 1J in that of the mandible, the latter is slightly concave, and ascends at an angle of about 35°. The length of the second dorsal spine is three-quarters of that of the head. Scales small. A black blotch on the spinous dorsal. Port Denison. (Klunzinger.; Species 384. Equula edentula. Bl. I have no doubt that E. coballa. Cuv. and Val., mentioned by Dr. Klunzinger as coming from Port Darwin and Cleveland Bay, is identical with E. edentula. Equula Novce Hollandice, Sleindachner from Cleveland Bay and Parequula bicomis of the same author from Hobson's Bay, Victoria, are both unknown to me and I have never seen the descriptions. Gen. Lactarius. Cuv. and Val. Body oblong, compressed, covered with cycloid scales of moderate size ; cleft of the moutli wide, oblique, with the lower jaw prominent. Teeth in the jaws small, with one or two pairs of strong canines ; teeth on the vomer and the palatine bones. 26 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Prpeopercular margin entire. The first dorsal with seven or eight feeble spines, continuous ; the second and the anal are more developed and scaly, without detached finlets. Three anal spines, continuous with the fin. Lateral line not armed. Head with muciferous cavities. Branchiostegals seven ; air bladder bifurcate anteriorly and posteriorly, the posterior branches united together behind the hasmal spine. Pyloric appendages in small number. East Indian Seas. 1184. Lactarius delicatulus. Bl. Schn. Gunth. Cat. 2, p. 507. Cuv. and Val. 9, p. 238. PI. 261. D. 7-8/^. A. 3/25-26. L. lat. 74. Ccec. pylor. 63. Vert, 10/14. The cleft of the mouth is very oblique and the lower jaw very prominent. Prseorbital much narrower than the maxillary. The interocular space is convex, and equal in width to the orbit. Coloration uniform ; sometimes with a black opercular spot. Queensland. (Klunzinger.) Family. NOMEIDiE. Genus Gasterochisma. Richards. Body oblong, compressed, covered with cycloid scales of moderate size ; cleft of the mouth wide. Lateral line without any armature. The first dorsal with seventeen spines ; the second and anal with the posterior rays detached, forming finlets , no separate anal spines, The ventral is exceedingly long and broad, and can be completely concealed in a deep fissure on the abdomen. Teeth conical, small, forming single series in the jaws, teeth on the vomer and the palatine bones. A New Zealand genus. 1185. Gasterochisma melampus. Richards. Voy. Ereb. and Terr., p. 60. Gunth. Cat. 2, p. 387. B. 7. D. 17/ 1/10 /VI. V. 1/5. A. 2/10 /VI. L. lat. 64. L. tr. 27. Ventrals black, one third of the total length. The maxillary reaches somewhat beyond the vertical from the centre of the eye. Mouth of the Derwent. (Johnston.) Length, 39 inches. BY WILLIAM MACLEAY, F.L.S., &C. 27 Family. SCOMBRI D^E. 1186. Scomber janesaba. Bleek. Gunth. Cat. 2, p. 359. D. 9-10 /£ /V-VI. A.l/10ln. /V-VI. Scales small, conspicuous. The height of the body is 6t-6§ in the total length, the length of the head four times ; the diameter of the eye 3J-3^ in the latter. Back with greenish- violet spots and waving transverse streaks ; sides and belly silvery. An air bladder. Hobson's Bay. ^Klunzinger). 1187 Scomber kanagurta. Russ. Gunth. Cat. 2 p. 360. Syn. S. loo. Cuv. and Val. S. chryzo- zonus. Riipp. S. microlepidotus. Riipp. *S'. moluccensis. Bleek. and S. reani. Day. D. 9-10 /A /V. A. l/i /V. Scales small. The height of the body is four times in the total, length of the head 3J. Above uniform greenish, on the sides and belly silvery, sometimes with longitudinal stripes on the back and sides, and with four or five blackish spots along the base of the spinous dorsal fin. Queensland. (Klunzinger.) 1188. Scomber tapeinocephalus. Bleek. Gunth. Cat. 2 p. 361. The Tunny of the Mediterranean. D. 11-11/A /V-VL A. l/i /V-VI Scales small, conspicuous, those of the pectoral region larger than the others. The height of the body is seven times in the total length, the length of the head i\. Teeth conspicuous. Back and sides with greyish violet spots and waving transverse streaks. No air bladder. Hobson's Bay. (Klunzinger.) 1189. Thynnus thynnus. L. D. 14/A/IX. A. 2/12/VIII. Vert. 16/23. The height of the body is 4^ in the total length, the length of the head four times. The pectoral reaches nearly to the end of 28 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, the spinous dorsal ; dorsal spines rather feeble. The posterior margin of the prceoperculum is somewhat shorter than the inferior. Above dark bluish ; beneath greyish, spotted with silvery. Tasmania. (Johnston) 1190. Cybium semifasciatum. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VIII., p. 205, Lower Burdekin, in salt water. Family. TRACHINIM]. 1191. Percis Coxii. Ramsay. Proc. Linn. Soc, N. S. Wales, Vol. VIII., p. 179. Loc. Port Jackson. 1192. SlLLAGO SIHAMA. Forsk. Gunth. Cat. 2, p. 243. Bleek. Atl. Ichth. Sillag., tab. 1, fig. 4. D. 11/i. A. 1/22-23. L. lat. 70. L. tr. 4/11. Coec. pyl. 2. Vert. 14/20. The height of the body is one-sixth of the total length, the length of the head one-fourth. The space between the eyes is one-half of the length of the snout. The ventral spine feeble. Coloration uniform brownish yellow, with a silvery lateral streak; fins transparent, reddish-violet. Queensland. (Klunzinger. ) Genus. Pseudochromis. Riipp. Head and body rather compressed, more or less elongate ; cleft of the mouth slightly oblique, with the lower jaw longest ; eye lateral. Scales of moderate size, ciliated ; lateral line interrupted. One dorsal with a few spines anteriorly ; ventrals thoracie ; the lower pectoral rays branched. Jaws with cardiforrn teeth, anteriorly with canines ; vomer and palatine bones toothed. Praioperculum entire. Six branchiostegals ; the gill-membranes joined inferiorly ; pseudobrauchia? and air bladder present ; pyloric appendages none. Indian Seas. 1193. Pseudochromis Mulleri. Klunz. Sitzb. der K. Akad. der Wissensch, 1879, p. 370. D. 3/23-24. A. 3/13. F. 18. V. 1/5. L. lat. 36. L. tr. e. 14. BY WILLIAM MACLEAY, F.L.S., &C. 29 Height of body and length of head 4^ in the total length. In front ot both jaws two strong canine teeth, and strong canine- teeth also on the sides ; there are besides narrow bands of small canine teeth on jaws, vomer and palatine bones ; 3 to 4 rows of scales on the cheeks ; 3 spines on the operculum. Prseorbital and prseopercuhim without serration. All the fins with long rays, particularly the dorsal, 'the middle rays of which are as high as the body. The caudal fin is rounded ; the ventrals extend to the anal fin ; the pectorals are a little shorter. The lateral line reaches to the 17th dorsal ray. Colour (in spirits) blackish brown ; head with many small blue spots. 6| Ctm. Port Darwin. (Klunzinger.) This fish seems to resemble very closely mv Cichlopsjilamentosus species 423 of catalogue. Family. BATRACHLD^E. 1194. Batrachus punctatulus. Ramsay. Proc. Linn. Soc, N. S. Wales, Vol. VIII., p. 177. Torres' Straits. 1195. Batrachus Mulleri. Klunz. Sitzb. dar K. Akad. der Wissensch., 1879. Tab. IX., fig 1. D. 3/20-21. A. 17. Height 5, and head 3* in total length. Like B. diemensis. No scales, body near the pectoral fins with reticulate folds of skin, 2 spines on the operculum and two on the suboperculum, the lowest small but distinct. Teeth villiform in bands on jaws, vomer and palatines. The maxillary extends to below the middle of the eye. Snout short, transversely vaulted. Forehead between the eyes broad, flat, much smaller than the orbit. The orbital cirrhus very minute, as also those of the head and back. Colour brownish with brown spots and a few larger dark specks, particularly one under the middle of the second dorsal fin. Head and forepart of back with thickly set alternately brown and lighter longitudinal stripes, 14 Ctm. Port Darwin, (Klunzinger.) 30 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Genus. Porichthys. Head broad, depressed ; body subcylindrical anteriorly and compressed posteriorly ; skin naked, with many series of very distinct pores. A canine tooth on each side of the vomer. Operculum with a single spine. The spinous dorsal formed by two very small spines. Gill-opening not narrow, extending downwards to the side of the isthmus. Gills three, pseudobranchise none, branch iostegals six ; air bladder more or less deeply divided into two lateral parts. Pyloric appendages none. Coasts of America. 1196. Porichthys Queexslandle. De Vis. Proc. Linn. Soc., N. S. Wales. Vol. VII., p. 370. Queensland. Family. PEDICULATI. Species 430 and 431. Brachionichthys hirsutes and B. kevis, are considered by Mr. Johnston. (Proc. Roy. Soc, Tasmania, 1882, p. 121) to be identical. Family. COTTINA. 1197. Platycephalus speculator. Klunz. Archiv. fur Naturg., XXXVIII, 1872. Sitzb. der K. Akad der Wissensch., 1879, tab. IV, fig. 1. D. 1/7-12. A. 13. P. 17. L. lat. 85. Height of body 14 times in the length, and length of head 4 times in the total length, and 3 J times its height and 1 J times its breadth , Resembles P. insidiator, but with the eye much larger, forehead and praeorbital narrower, and parallel supraorbital crests, which in P. insidiator converge backwards. The point of the tongue is in this species spatulate and prominent, in the other species truncate. It differs also in the number of the dorsal rays, being 12 in this as against 13 in P. insidiator. The lower prseopercular spine is a little longer than the upper. The colour resembles that of P. insidiator, the fins have a rather greener hue and not brown-spotted. Hobson's Bay. (Klunzinger.) BY WILLIAM MACLEAY, F.L.S., &C. 31 1198. Platycephalus Mulleri. Klunz. Sitzb. der K. Akart. der Wissensch, 1879, tab. IV., fig. 2. D. 1/8/12. A. 12. L. lat. 100. L. tr. 35. Head 4, height 9^ in the length. Most like P. inops. Head broad and flat, particularly in front. Teeth villiform in a broad band in the upper jaw, narrower in the lower, vomerine teeth in two longitudinal stripes separated bv a groove. Eye rather small. Ridges on head distinct but not prominent, with a few recumbent spines. A larger spine in front of the inner and upper angle of the eye. No spine on the preeorbital. Only one of the spines of the preeoperculum properly developed (the upper), and that is short, the inferior one is merely a small obtuse tubercle. Lateral line not conspicuous. Colour grey, the scales mostly with darker specks. Head above darker, brown marbled. Belly white or yellowish. Rays of doi'sal fin with darker rings ; the membrane light ; pectoral fins light ; ventrals above dirty brownish-grey ; caudal with white and dark speckled rays, the lower margin and the upper extremity black. Dr. Klunzinger gives no locality for this species. 1199. Platycephalus Mortoni. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VIII., p. 206. Lower Burdekin. Salt water. 1200. Platycephalus semermis. De Vis. Proc. Linn. Soc, N. S. Wales, Vol. VIII., p. 285. South Australia. 1201. Lepidotrigla Mulhalli. Macleay. Proc. Linn. Soc, N. 8. Wales, Vol. VIII. Outside Heads of Port Jackson. Family. GOBIID.E. 1202. Gobius nebulopunctatus. Cuv. and Val. Gunth. Cat. III., p. 20. D. 6/i. A. 1/8. L. lat. 85. 32 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, " The height of the body is contained six times in the total length, the length of the head four times and two-thirds. The head is nearly as broad as high, its height being more than one- half its length. The diameter of the eye is one-fourth of the length of the head ; it is situated entirely in the anterior half of the head, interorbital space very narrow. Snout as long as the eye, with the cleft of the mouth oblique, and with the jaws equal in length. The teeth in the jaws form a band, those of the outer series being somewhat enlarged. Dorsal fins separated from each other but close together ; the first is lower than the second, the height of which equals that of the body. The upper pectoral rays silk like ; caudal rounded ; the anal is much higher posteriorly than anteriorly ; its height being equal to that of the second dorsal fin. Greenish, clouded with brownish ; head and body with longitudinal series of numerous white dots ; fins uniform blackish, the first dorsal edged with white superiorly." King Geoi'ge's Sound and Victoria. (Klunzinger.) 1203. Gobius Tamarensis. Johnston. Prcc. Roy. Soc. Tasmania, 1882, p. 120. B. 4. D. 6i. A. 1/8. L. lat. 32. P. 16-18. P. 18-19. Height of body seven times in total length, the length of head four times, and the greatest breadth behind orbits six times. Head depressed ; eyes approximating towards top of head, looking upwards and outwards. Snout obtuse, convex, one and a-half times breadth of eye, and contained three and a-half times in length of head ; interorbital space, half the breadth of the eye ; head and nape naked. Colour, when alive, greyish. Body and vertical fins marbled with very fine reddish -brown dots. The extremity of the rays of second dorsal and anal fins blackish. There are eleven scales between the anal and the first ray of the second dorsal fin ; caudal fin rounded ; dorsal and anal fin rays one and a-half times as long as the snout, when stretched they do not reach the caudal by a distance gr-eater than their own length." Abundant in the Tamar River. Length from 2 to 3J inches. Mr. Johnson remarks that the species seems to closely resemble G. lateralis. Macleay. BY WILLIAM MACLEAY, F.L.S., &C. 33 1204. Eleotris Selheimi. Macleay. Eleotris ])laniceps. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 69. Palmer River, N. Queensland. The specific name planiceps has been previously used by Count Castelnau for a species (525), from the Norman River. 1205. Eleotris aporocephalus. Macleay. Eleotris planiceps. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 20G. Lillesmere Lagoon. Burdekin River. This I think is probably the species which Klunzinger refers to E. porocephaloides. Bleeker. 1206. Eleotris cyprixoides. Cuv. and Val. Gunth Cat. III., p. 118. Klunz. Sitzb. der K. Akad. der Wi.s.sensch., 1879, tab. V. fig. 2. D. 6/i. A. 1/9-10. L. lat. 26-28. Head entirely scaly. Body compressed, its height being nearly equal to the length of the head, and one-fifth of the total ; the diameter of the eye is rather more than one-fourth of the length of the head, equal to the width of the interorbital space, and longer than the snout. Snout pointed, with the lower jaw longest ; the maxillary does not extend to the vertical from the anterior mai'gin of the eye. Teeth in villiform bands. Scales finely ciliated. Brownish-olive, with a blackish longitudinal band from the upper part of the base of the pectoral, below the lateral line to the caudal ; dorsal and caudal fins with brown spots. Murray River. (Klunzinger.) 1207. Eleotris reticulatus. Klunz. Sitzb. der K. Akad. der Wissensch.. 1879, p. 385. Tab. 4, fig 3. D. 6/J. A. 1 10. L. lat,, 28-30. L. tr. 10. Height of body and length of head 5 times in the total length The caudal peduncle equals the length of the head. Colour yellowish or brownish, the dark margins of the scales giving the appearance of reticulate markings. Fins dark, marbled or speckled. 34 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, On the base of the caudal fin in its lower half, there is a darker spot, generally also one above the base of pectoral fin. Scales fine and equally toothed. 4 Ctm. Port Darwin. (Klunzinger.) 1208. Eleotkis macrodon. Bleek. Gunth. Cat. III., p. 129. Klunz. Sitzb. der K. Akad. der Wiss., 1879, p. 385. D. 6/10-11. A. 9. Lat. 90-100. L. tr. 30. Thirty-three longitudinal series of scales between the origin of the posterior dorsal and the anal, sixty transverse ones between the anterior dorsal to the snout. The height of the body is contained four times and two-thirds or five times in the total length, the length of the head four times and a fourth. Head broad, depressed, with the snout obtuse ; the lower jaw is some- what prominent, and the maxillary extends to below the middle of the eye. Teeth of the outer series enlarged. The diameter of the eye is one-ninth of the length of the head, one half of that of the snout, and one-third of the width of the interorbital space. A small barbel on each side of the upper jaw. The head is covered with minute scales, the snout is naked. Dorsal and anal fins much lower than the body ; the greater portion of the caudal is scaly ; its length is about one seventh of the total. Brownish- olive (in spirits) ; dorsal and caudal fins dotted with brown, the other fins uniform. A blackish (in life reddish-brown) ocellus, edged with whitish, on the upper part of the base of the caudal. Port Darwin. (Klunzingei\) 1209. Aristeus cavifruns. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 70. Palmer River. Genus Leme. De Vis. Group amblyopina. Proc Linn, Soc, N. S. Wales, Vol. VIII, p. 286. Queensland. 1210. Leme mordax. De Vis. Proc. Linn. Soc, N. S. Wales, Vol VIIL, p. 286. BY WILLIAM MACLEAY, F.L.S., &C. 35 1211. Callionymus achates. De Vis. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 620. Queensland. 1212. Callionymus phasis. Guntli. Zool. Voy. Challenger. Part 6., p. 28. PL 15, fig. C. D. 4/9. A. 7. C. 10. Preeopercular spine considerably shorter than the eye, terminating in three curved spines, of which the two anterior are the larger, and directed upwards. Dorsal spines prolonged ; second dorsal high ; caudal long ; the ventral fin extends somewhat beyond the origin of the anal. Gill-opening reduced to a small foramen on the upper side of the neck ; lateral line single. The length of the head is one-third of the total length without caudal, or one-fourth with that fin. Eye very large, a little longer than the snout, one-third of the length of the head. Reddish-white with irregular broad blackish cross-bands on the back ; first dorsals blackish, with some whitish zig-zag lines ; second, variegated with greyish ; the other fins white. Length of specimens 4 inches." Twofold Bay. 120 fathoms. 1213. Callionymus lunatus. Schleg. Gunth. Cat. Ill, p. 146. Zool. Voy. Challenger. Part 0, p. 28. D. 4/9. A. 9. V. 1/. P. 17. C. 10. About 8 inches in length. The orifices of the gills, the nostrils, the pectorals, and ventrals as C. Valenciennei. The superior border of the orbit is prominent, and the space between the eyes very narrow and concave. Top of the head naked and rough. The osseous production of the preeoperculum has a superior spine at right angles to a larger one. The two dorsals are of about equal height which is higher than that of the body; but the last three rays of the 2nd dorsal are longer than the others, the 1st spine of the 1st dorsal is twice the length of the others, and the membrane of the last dorsal spine is continued to the base of the 1st ray of the 2nd dorsal. The anal is one-third lower than the dorsals and its rays, with the exception of the last, are simple. The 36 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, caudal is of elongate form, its length about 3J in the total length. The pectorals are a little conical. Colour pale reddish brown, becoming white on the belly. The root of the caudal and the ventrals inclining to a deep brown. The anal has large blotches and the ventrals longitudinal streaks of pale brown. The membrane which unites the last dorsal spine to the back has a large black blotch bordered towards the base with white. Port Jackson. (Gunther.) Family. TRICHONOTID^S. Genus. Hemeroccetes. Cuv. and Yah Head depressed, pointed, trunk cylindrical, tail slightly com- pi'essed ; cleft of the mouth wide, nearly horizontal, with the upper jaw longest ; eyes rather large, directed upwards. Scales of moderate size, cycloid ; lateral line continuous. One dorsal ; all the rays articulated and not branched : ventrals jugular with one spine and five rays. Gill-opening very wide, with the gillmem- branes scarcely united below the thi-oat ; seven branchiostegals ; pseudobranchire. Villiform teeth in both the jaws, on the vomer, and on the separated pharyngeal bones ; none on the palatines. Air-bladder and pyloric appendages none. A New Zealand genus. 1214. Hemerocoztes Haswelli. Ramsay. Proc. Linn. Soc, N. S. Wales, Vol. VI., p. 575. Port Jackson. Dredged in 10 fathoms at North Head Family. BLENNHD^E. 1215. Salarias Mulleri. Klunz. Sitzb. der K. Akad. der. Wissensch., 1879, p. 388. D. 12/20. A. 23-24. Height 8, head 5h in the total length. Rather elougate, low, crested on the neck ; orbital cirrhus simple, shorter than the eye ; profile of head perpendicular or even sloping inwards towards the snout. No canine teeth. Dorsal fin deeply notched ; the 1st dorsal a little lower than the 2nd, a little over the height of the body, and as high as the anal fin ; the second dorsal connected with the caudal fin which is rounded. Colour brownish, BY WILLIAM MACLEAY, F.L.S., &C. 37 in the middle of the body numerous narrow transverse bands with dark margins, not quite reaching either the back or the belly, and becoming less distinct and somewhat undulating posteriorly. On the anterior part of the body there are some bluish transverse bands convex anteriorly. Belly and side of breast colourless. Crest of nape with black margin. Dorsal fin, with numerous oblique bluish streaks, anal with blue spots or streaks towards the margin in about four rows. Caudal with numerous white or blue spots. 7 Ctm. Affinity to S. geminatus. All. and Macleay. Hobson's Bay. (Klunzinger.) 1216. Salarias punctillatus. Klunz. Sitzb. der K. Akad. der Wissensch., 1879, p. 389. D. 12/20. A. 20. V. 2. Height 5 and head 6 times in the total length. Like S. onyx. Cuv. and Val. Profile of head in front vertical. Short small cirrhi round the eye, nostrils, and nape, those round the eye bifid, and about half the diameter of the eye, the others simple. Dorsal fin without notch, the first ray is only 1/3 higher than the last ; it is connected with the caudal fin ; the anal fin is not. The caudal is rounded. The lateral line is bent in front and terminates under the 8th dorsal ray. Crest of nape distinct but very low. Forehead nearly flat. Colour (in spirits) brownish, with indistinct darker or lighter specks which form transverse bands. The belly and breast whitish ; dorsal fin greenish, indistinctly spotted ; pectoral, anal and caudal fins monochromatic greenish. On the head there are white and blue spots and lines, and on the back posteriorly there are a few scattered small spots. 10 Ctm. Port Darwin. (Klunzinger.) Dr. Klunzinger alludes to the similarity of this to S. Spaldingii mihi ; they are I think distinct. 1217. Clinus mamoratus. Klunz. Archiv. f. Naturg. XXXVIII. , 1872. Sitzb. der K. Akad. der Wissensch., 1879. D. 44. A. 30. P. 13. V. 3. C. 10. 38 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Height (in front of the anus) 5 times in the length, length of head six times. Body elongate, compressed : profile of head parabolic ; snout obtuse, short, teeth in both jaws, arranged in a band in front, and on the sides in a row short and blunt. Teeth on the vomer, none on the palatines ; the maxillary reaches to below the middle of the eye ; space between the eyes narrower than the orbit. Head and occiput nearly naked ; body covered with small indistinct round scales. Lateral line only visible on the anterior part of the body. The dorsal fin begins over the operculum, and gets higher towards the caudal with which it is connected with a membrane ; anal fin similar, also with simple flexible rays. Colour brown with darker spots, marbled, throat sometimes white speckled ; fins black speckled, marbled with some lighter spots ; pectoral fins lighter with dark spots. Allied to C. cottoides and desincillatus. Length, 15 Ctm. Port Phillip. (Klunzinger.) 1218. Cristiceps tristis. Klunz. Archiv. f. Naturg., 1872, p. 31. Sitzb. der K. Akad. der Wissensch., 1879, p. 392. D. 3/19/5. A. 2/24. P. 11. V. 3. C. 9. Height 5 1 in length. Body elongate, very much compressed. Profile of head nearly straight. Snout pretty long ; lips much developed : jaws ecpial ; on both and on the vomer a band of small hair-shaped teeth, broader in front of the prsemaxillary. The maxillary reaches to below and rather behind the middle of the eye. Orbital cirrhus over the middle of the eye, flattish and fringed ; nasal cirrhus small, tubular and with a flat flap above. Head and nape nearly naked and smooth. The first part of the dorsal fin is on the occiput over the prasoperculum, it is higher considerably than the rest of the fin, with which it is -connected by a membrane. The dorsal rays are pretty strong, and the fin membranes form a flap behind their apices ; the fin membrane extends from the last dorsal ray to the base of the caudal fin. The anal fin commences under the 9th ray of the 2nd division of the BY WILLIAM MACLEAY, F.L.S., &C. 39 dorsal fin ; it is lower than the dorsal, and the fin membrane does not nearly reach the caudal. Tiie pectoral fin is short and rather high, it extends to the anal fin ; the middle ray of the ventrals also reaches to the anal. Scales small but distinct, leathery, shining, etenoid, only slightly imbricate. Lateral line marked with simple strise ; it ascends from the upper margin of the branchial aperture, then is strait to the 8th dorsal spine, then descends abruptly and then runs straight to the tail; caudal fin narrow and slightly rounded. Colour monochromatic dark brown. 16 Ctm. Murray River. (Klunzinger.) Family. SPHYR^ENID^E. 1219. Sphyilena strenua. De Vis. Proc. Linn. Soc. N. S. Wales. Vol. VIII., p. 287. Moreton Bay. Family. ATHERINIILE. 1220. Atherina elongata. Klunz. Sitzb. der K. Akad. der Wissenscb., 1879, p. 394, Tab. III. fig. 4. D. 6-7,1 A. 1/11-12. L lat. 40. L. tr. 7. Nearly related to A. •pingids and valenciennesii. The body however is larger and the rays more numerous. The vomerine teeth are present. The 1st dorsal fin commences just behind the pectorals ; the anal is a little longer than the 2nd dorsal, but terminates exactly opposite to it. Apophysis of the maxillary very short. Colour as usual in the genus, the silvery band is on the third line of scales. Fins hyaline. 7-8 Ctm. King George's Sound. (Klunzinger.) 1221. Atherinichthys esox. Klunz. Archiv. f. Naturg., 1872, p. 34. D. 7|A- A. 1/12. R 12. L. lat. 45. L. tr. 8. Height 7 times in the length, length of head 3 J. Elongate, lancet shaped, rather compressed ; profile straight ; snout very prominent, pointed. Maxillary very protractile ; head flat above. 40 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Gape of mouth very obliqiie, extending only to the middle of snout. The narrow sword shaped upper jaw reaches to below the middle of the eye. A narrow stripe of small but distinct teeth in both jaws ; the vomer is toothed, but not the palatines. Scales large, no distinct lateral line ; spines of 1st dorsal fin weak and short ; the 2nd dorsal and anal alike ; the pectoral does not reach quite to under the 1st dorsal spine. The ventrals are inserted before the point of the pectorals, and extend nearly to the last dorsal spine, but not nearly to the anus. Caudal fin forked. Colour above dark, beneath silvery, a broad silvery blue band along the middle of the body. Length, 14 Ctm. Port Phillip. (Klunzinger.) 1222. Atherinichthys maculatus. Macleay. Proc. Linn. Soc, K S. Wales, Yol. VIII., p. 207. Lillesmere Lagoon, Burdekin. Family. MUGILID^E. 1123. Mugil tade. Forsk. Mugil planiceps Cuv. and Val. Gunth. Cat. III., p. 428. D. 4/|. A. 3/9. L. lat. 33-35. L. tr. 11. Ccec. pylor. 5. The greatest depth of the body is nearly equal to the length of the head, and one-fifth of the total ; the depth of the body below the origin of the spinous dorsal is contained twice and a third in the distance of the snout from the dorsal fin. The least depth of the tail is a little more than one-half the length of the head. Lips thin ; the maxillary is bent downwards behind the angle of the mouth, its extremity not being covered by the prseorbital. The space at the chin, between the mandibulary bones, is cuneiform. Eye with a narrow adipose membrane, which does not extend on to the pupil. There are twenty scales between the snout and the spinous dorsal. The eight, the tenth, or eleventh, the twenty- second or twenty-third scales of the lateral line correspond to the extremity of the pectoral, and to the origin of the two dorsal fins. The soft vertical fins scaly ; the origin of the dorsal is in the vertical from the third soft anal ray. Cleveland Bay. (Klunzinger.) BV WILLIAM MACLEA.Y, F.L.S., &C. 41 1124. Mugil LONGIMANUS. Gunth. Cat. Ill, p. 428. D. 4/i. A. 3/9. L. lat. 35. The height of the body is contained four times and two-thirds or five times in the total length ; the length of the head five times or five times and a fourth. The width of the interorbital space is about one-half the length of the head. Eye with an adipose membrane anteriorly and posteriorly. Snout very convex, with the upper lip rather thick. The maxillary is entirely hidden when the mouth is closed. The two dorsal fins and the anal are nearly equal in height ; pectoral about as long as the head ; caudal truncated." Cleveland Bay. (Klunzinger.) 1125. MUGIL GELATINOSUS. KluDZ. Archiv. fur Naturg., 1872. Sitzb. der K. Akad. der Wissensch, 1879, Tab. VIII., fig. 1. D. 4/J. A. 2/8. P. 15. L. iat. 42. L. tr. 12. Height of body oh, and length of head 5 times in the total length. Body elongate, rather compressed. Profile of head at the snout a little convex ; forehead transversely slightly convex ; upper lip thick, on both lips small cilia, knot of the under jaw simple. Groove of the vomer deep. Lower margin of the prae" orbital straight without serrature. Maxillary narrow posterioi'ly, not hidden under the praaorbital, and not reaching the anterior margin of the eye. The eye has highly developed anterior and posterior lids, with a gelatinous mass in front and behind. The space on the chin is of an elongate lance-shape. The margin of the operculum is simply curved. Scales lai'ge, conspicuous and striated, the stria? on the breast a little oblique. The 1st spine of the 1st dorsal is situated in the middle of the body (excluding the caudal fin) it is short and strong, the others are slender and flexible ; the anal is situated a little nearer the head than the 2nd dorsal. Pectorals short, triangular, 1£ in the head ; ventrals a little shorter; caudal deeply forked, forks pointed. Colour as usual, pectoral fin blackish behind, margin hyaline ; 2nd dorsal and caudal blackish margined. 45 Ctm. Hobson's Bay. (Klunzinger.) 42 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, 1126. Mugil Mulleri. Kluuz. Sitzb. der K. Akad. der Wisscnsch., 1879, p 395. D. 4/J. A. 3/8. L. lat. 38-40. L. tr. 14. Height 41 and head 4 times in the total length. Nearly related to M. suj)positus. Gunth. but of different dimensions. Month in front angular, pointed ; upper lip narrow ; both lips with well developed cilia ; keel of the under jaw simple ; prseorbital toothed on its posterior margin ; the posterior small end of the maxillary not. Head scaly above as far as the lip ; dorsal rays stiff but not thick. Eye without adipose membrane. Colour simple, silvery ; fins without black magin ; no axillary spot. 8 Ctm. King George's Sound. (Klunzinger.) 1227. Mugil nasutus. De Vis. Pro. Linn. Soc, N. S. Wales, Vol. VII., p. 621. Rockingham Bay. 1228. Mugil Ramsayi. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VTIL, p. 208. Burdekin River. Family. CENTRISCID^E. 1229. Centriscus gracilis. Lowe. Proc. Zool. Soc, 1839, p. 86. Gunth. Cat. III., p. 521. B. 4. D. 4-5/11. A. 18-19. P. 16. V. 5. C. 6 x 4 x 5 x 6. The height of the body is contained twice and three-fifths to three times in the distance of the operculum from the base of the caudal fin. The second dorsal spine is rather strong, not (or very indistinctly) denticulated posteriorly, its length being one-fourth or two-ninths of the distance of the operculum from the caudal. Port Jackson. (Macl. Mus.) C scolopax I have never seen here. Mr. Johnston's scohpax is probably this species, Family. GOBIESOCID^E. Genus Gobiesox. Lacep. Anterior part of the body very broad and depressed ; skin tough. Snout very obtuse. Dorsal fin short, situated on the tail. BY WILLIAM MACLEAY, F.L.S., &C. 43 Posterior portion of the adhesive disks without free anterior margin. Distinct incisors in the lower jaw ; those of the upper jaw are in several series, and the interior ones sometimes compressed. Gills three, pseudobranchiaB rudimentary ; gill-membranes united under the throat, and not attached to the isthmus. West Coast of South America, &c. 1130. Gobiesox cardinalis. Eamsay. Proc. Linn. Soc. N. S. Wales. Vol. VII., p. 148. Tasmania. Family. TRACHYPTERD^. Genus. Trachyterus. Gouan. Body elongate, strongly compressed, naked ; eye lateral ; mouth small, dentition feeble. One dorsal fin occupying the whole back, with a detached anterior portion, composed of flexible rays. Ventrals thoracic, well developed, composed of several more or less branded rays. Gill-opening wide ; pyloric appendages in very great number. Vertebrae numerous. Bones soft, muscles little coherent. Coasts of Europe. Pacific Ocean South. 1231. Trachypterus altivelis. Kner. Gunth. Cat. Ill, p. 303. B. 6. D. 7/190. A. 0. C. 6/4-6. P. II. V. 7. " The greatest height of the body is above the ventral fins, equal to the length of the head, and one seventh of the total. Form of the head as in T. tcenia. Eight teeth in the upper and six in the lower jaw. The anterior dorsal rays elevated ; the longest of the second dorsal fin are not much lower than the body ; dorsal rays rough, with a small spine at the base of each, Form of caudal fin and tubercles as in T. tcenia. Silvery, with three large round black spots below the dorsal fin ; a fourth near the abdominal edge, a little behind the first on the back." A specimen taken at Spring Bay, East Coast of Tasmania, and now in the Museum, Hobart. (Johnston.) 14: SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Family. POMACENTRIDJS. 1232. Pomacentrus trilixeatus. Cuv. and Val. Gunth. Cat. IV, p. 25. Bleek. Atl. Ichth. Pomac, tab. 7, fig. 1-6. D. 13/15. A. 2/16. L. lat. 28. L. tr. 3/9. " The height of the body is contained twice and three-fourths in the total length ; prseorbital denticulated, with two stronger teeth anteriorly. The dorsal spines increase in length towards behind ; caudal emarginate, with the lobes rounded. Greenish-olive (in spirits brown) ; the base of the caudal itself yellowish, each scale with one, two, or three sky-blue dots ; three or five very fine blue lines along the forehead, the outer of which are continued on the nape of the neck and sometimes along the base of the dorsal fin ; a round dark spot above the operculum ; a black spot edged with blue on the back of the tail, immediately behind the dorsal fin ; young specimens with a second similar spot on the anterior third of the soft dorsal fin." Port Darwin and Port Denison. (Klunzinger.) 1233. Pomacentrus t.eniurus. Bleek. Atl. Ichth. Pomac. tab. 9, fig. 2. Gunth. Cat. IV, p. 22. D. 13/11. A. 2/11. L. lat, 28. " The height of the body is contained 3| to 3* in the total length ; prreorbital not serrated. The posterior dorsal spines are nearly as long as the middle ones ; caudal fin with the lobes pointed and produced. Violet-olive, each scale with a pearl- coloured spot ; a blackish spot above the operculum and above the base of the pectoral fin. Dorsal and anal fins dark-violet, the posterior half of the soft portion and the pectorals orange- coloured, caudal orange-coloured, with a dark-violet longitudinal band on each lobe." Port Denison. (Klunzinger.) 1234. Pomacentrus cyanospilus. Bleek. Atl. Ichth. Pomac. tab. 4, fig. 5. Gunth. Cat. IV., p. 30. D. 12/15. A. 2/13-14. L. lat. 26. L. tr. 3 9. BY WILLIAM MACLEAY, F L.S., &C. 45 " The height of the body is contained twice and two-thirds in the total length. There is no notch between the prreorbital and the other suborbitals, their lower or posterior margin being equally and finely serrated. The dorsal spines become gradually longer posteriorly. Caudal rather deeply emarginate, with the lobes rounded. Brownish, sides of the head and the scales above the anal fin with round bluish spots ; anal and dorsal fins very dark posteriorly ; axillary or dorsal spots none." Port Darwin. (Klunzinger ) 1235. Pomacentrus fasciatus. Cuv. and Val. Gunth. Cat., IV., p. 19. B. 5. D. 12-13/13. A. 2/12-13. L. lat. 27. L. tr. 3/9. The height of the body is contained twice and three-fourths in the total length ; prreorbital denticulated. The dorsal spines increase in length posteriorly ; caudal very slightly emarginate. Brown, lighter beneath, with four yellowish cross-bands ; one from the neck to the operculum, the second from the front part of the dorsal fin to behind axil of the pectoral, the third from the posterior dorsal spines, and the fourth, spot-like, on the back of the tail ; two parallel series of black spots from the opercle along the side of the trunk." Port Darwin. (Klunzinger.) 1236. Glyphidodon melanopus. Bleek. Alt. Ichth, Pomac. tab. 8, fig. 7. Gunth. Cat. IV. p. 48. D. 13/13. A. 2/13. L. lat. 28. The upper profile of the head is convex ; snout shorter than the eye ; the width of the prseorbital, above the angle of the mouth, is less than one-half of that of the orbit. Each jaw with about forty teeth. Yellow ; most of the scales with a blue spot ; the anterior portion of the ventral and anal fins black. Port Denison. (Klunzinger.) Species 680. Heliastes hypsilepis. Gunth. Additional habitat. Kins George's Sound. (Klunzinger.) 46 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Family. LABRID^E. Genus Platychosrops. Klunz. A genus intermediate between Chceroj>s and Heterochcerops, with the latter it agrees in the number of dorsal spines (only 11) with the former in the great altitude of the prseorbital. Peculiai', are the very flattened spines of the dorsal and anal fins, and the partially incisor like character of the front teeth ; the scaley sheath for the dorsal and anal fins is highly developed. 1237. Platychcerops Mulleri. Klunz. Sitzb. der Akad. der Wissensch., 1879, p. 399. Tab. VIII. fig. 2. D. 11/11-12. A. 3/11-12. L. lat. 36-38. L. tr. 8/12. Height 3^-3f , and head 4 times in the total length. The front teeth are flat, not conical, the lateral teeth as in Chserops. The upper lip is large and flat, leaf-shaped, the under similar but thicker. The scales of the cheeks are non-imbricate ; the margin of the prreoperculurn, around the eyes, the forehead, the snout, the prseorbital, the lips and the chin are uaked. The scales of the nape are small, those of the operculum of medium size, and those of the body large. Lateral line continuous with slightly branched ramifications. Eyes small ; dorsal spines flat, knife-shaped, except the 4 posterior ones and the two anterior anal rays. Ventrals shorter than the pectorals ; caudal truncate ; dorsal and anal rays higher than the spines. Of very robust form. Colour dirty grey-green, head brown, fins livid. 28 Ctm. King George's Sound. (Klunzinger.) 1238. Trochocopus sanguinolentus. De Vis. Proc. Linn. Soc. N. S. Wales, Vol. VIII. , p. 287. Cape Moreton. 1239. Cossvphus Frenchii. Klunz. Sitzb. der K. Akad. der Wissensch., 1879, p. 400. D. 12/10. A. 3/11. L. lat. 35-37. L. tr. 4/12. I give this species a place in my catalogue, but Dr. Klunzinger is very doubtful as to whether it is not identical with my BY WILLIAM MACLEAY, F.L.S., &0. 47 Trochochojms rufus. If it be the. same fish, he is certainly not justified in changing the genus and name of the species. The differences in the descriptions are of the most trivial description. 1240. Labrichthys dux. De Yis. Proc. Linn. Soc, 1ST. S. Wales, Vol. VIII, p. 287. Moreton Bay. Genus. Novacula. Cuv. and Val. Body compressed, oblong, covered with scales of moderate size ; head compressed, more or less elevated and obtuse, with the upper profile generally more or less parabolic ; head nearly entirely naked, or with small scales on the cheek ; lateral line interrupted. No posterior canine tooth. D. 9/12. A. 3/12, the two anterior dorsal spines sometimes remote or separate from the other. Tropical Seas. 1241. Novacula Jacksoniensis. Bamsay. Proc. Linn. Soc, N, S. Wales, Vol. III., p. 198. Port Jackson. 1242. Coris semicincta. Bamsay. Proc. Linn. Soc. N. S. Wales. Vol. VII., p. 301. Broken Bay. Lord Howe's Island. Species. 762. Siphonognathus argyrophanes. Four specimens of this very curious fish were received lately by the Australian Museum from South Australia. In the character of the genus given by Dr. Gunther in his Catalogue, he has omitted to mention that there are no ventral fins. Family. GADID^F. 1243. Lotella Swanii. Johnston. B. 7. D. 4/60. A. 55. V. 8. P. 22-23. L. lat. 200. L. tr. 22/62. Head contained 4g times in total length, and greatest depth \\ times. Length of snout equal to diameter of eye, and about one- fifth the length of the head. Distance between orbits half again 48 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, as broad as diameter of eye. There is a series of 8 to 1 1 irregular teeth in upper and lower jaws. Scales small. Colour uniformly dark brown. Not common. (Johnston.) Tasmania . Genus. Physiculus. Kaup. Body elongate, covered with small scales. A separate caudal ; two dorsal fins and one anal • ventral fins with a very narrow but flat base, composed of several rays. Teeth in the jaws in a band, small, villiform, of equal size ; vomerine or palatine teeth none. Chin with a barbel. Branchiostegals seven ; gill-rakers of the outer branchial arch short. Madeira. 1244. Physiculus palmatus. Klunz. Archiv. fur Naturg., XXXVIIL, 1872. R. br. 7. D. 9/56. A. c. 50. L. lat. c. 120. L. br. c. 15/30. Height of body and length of head 4J in the length. Elongate, elliptic ; profile of head slightly parabolic, point of snout notched, forehead and preeorbital scaly ; under jaw retreating ; a pointed barbel on the chin about as long as the eye ; the maxillary reaches beyond the hind margin of the eye. There is a broad band of villiform teeth in both jaws, none on the vomer and palate. The 1st dorsal fin commences immediately behind the base of the pectoral, the 2nd dorsal opposite the anal ; the cauda} is quite separate and rounded. The ventrals are about half the size of the head, with the base narrow, but flat and not styliform. Colour brownish, dorsal anal and caudal fins brown-margined. Length, 50 Ctm. Port Phillip. (Klunz.) 1245. Pseudophycis breviusculus. Richards. Ramsay Proc. Linn. Soc., N. S. Wales, Vol. VI., p. 717. Port Jackson. Family. MACRURID^E. 1246. Coryph^enoides Tasmanle. Johnston. Proc. Royal Soc. Tasman., 1882, p. 143. B. 7. D. 15/103. A. 90. V. 8. BY WILLIAM MACLEAY, F.L.S., &C. 49 Snout short and obtuse, not projecting beyond mouth. Length nearly six times that of the head, which latter is longer than the greatest depth of body, and measures three times the length of snout. Diameter of eye scarcely equal to length of snout. Barbel rudimentaiy. Scales small, smooth, without ridges or spines. There are eight series .of scales between anterior dorsal and the lateral line. The lateral line is composed of about 133 series of scales, the pierced scales being interrupted. The first dorsal is composed of 15 feeble jointed rays, the length about twice the diameter of the eye. The second dorsal commences near to the termination of the first dorsal. The anus is situated under the 17th ray of the second dorsal, and neai'er to the snout than to the tail by twice the length of the snout. Uniform silvery plumbous. with a purplish shade. (Johnston.) Seen in shoals at some seasons between Port Davey and Macquarie Harbour, known as the " Tasmanian Whiptail." Family. PLEURONECTJD^]. Species 780. Pseudorhombus Russellii. Klunzinger makes the P. polyspilus Bleek, regarded by Gunther as a synonym of Russellii, as a different species. He is probably right, the markings and the dentition are certainly a little different. He gives King George's Sound as its locality. 1247. Pseudokhombus Mulleri. Klunz. Archiv. fur Naturg., 1872. Sitzb. der. K. Akad. der Wissensch., 1879, Tab. IX., fig. 2. D. 90. A. 73. V. 6. L. lat. 66. Body oval, elliptic ; profile of head convex. Teeth in both jaws in one row, small, rather unequal. Mouth oblique, jaws equal ; length of upper jaw 3 in length of head. Eyes close and directly above one another, the lower slightly in advance. The diameter of the anterior curved portion of the lateral line, \\ in the length of the head. The dorsal fin commences a little in front of the eye, the rays are of about the same height from the 10th to the 70th. Scales medium size, ciliated. Pectoral fin 4 50 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, narrow, 1^ in the length of the head ; ventral nearly 3 in length of head ; dorsal and anal nearly join the caudal. Colour uniform dark brown. 15 Ctm. Hobson's Bay. (Klunzinger.) 1248. Amjiotretts zonatus. Macleay. Proc. Linn. Soc., N. S. Wales, Vol. II., p. 367. Port Jackson. Genus. Pledronectes. Cleft of the mouth narrow, with the dentition much more developed on the blind side than on the coloured. Teeth in a single or double series, of moderate size ; palatine and vomerine teeth none. The dorsal fin commences above the eye. Scales very small or rudimentary, or entirely absent. Eyes generally on che right side. Temperate and Arctic Seas. 1249. Pleuronectes Moretoniensis. De Vis. Proc. Linn. Soc, N. S. Wales, Vol. VII., p. 370. Moreton Bay. 1250. Solea uncinata. Klunz. Sitzb, der. K. Akad. der Wissensch., 1879, p. 408. D. 77. A. 50. V. dextr. 7, sin. 4. P. 10. Height of body 2£, and length of head 3 times in the total length without caudal fin. L. lat. about 70 ; the highest dorsal and anal rays 3-^ in length of body, Body oval, scales small, lateral line straight ; pectorals of left side scarcely smaller than the other ; lower eye nmch advanced ; forehead small, protruding, scaly ; snout curved backwards under the chin, the dorsal rays extending to the point ; caudal fin long and rounded ; left nostril small. Colour uniform, slate-grey to black. Resembles S. liturata Richards. 15 to 20 Ctm. King George's Sound. (Klunzinger.) 1251. Solea fluviatilis. Ramsay. Proc. Linn. Soc. N. S. Wales. Vol. VII. p. III., Hunter River. BY WILLIAM MACLEAY, F.L.S., &C. 51 1252. Solea lineata. Ramsay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 406. Port Stephens. 1253. Solea (Achirus) poroptera. Bleek. Atl. Ichth. Pleuron.'p. 24. tab. 15, fig. 2. D. 67. A. 52. L. lat. 80. Dorsal and anal fins simple, or bifid at the top only. The height of the body is contained twice and a half or twice and two thirds in the total length. Eyes subcontiguous. Colour greyish- brown with numerous small blackish dots ; two brown blotches on the lateral line, and four others along the back. Probably the same as Aehirus thepassii. Bleek. Gunth. Cat. IV., p. 478. Port Darwin. (Klunzinger.) 1254. Synaptura fasciata. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 14. • Port Jackson. 1255. Synaptura Selhedii. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 71. Palmer River. Fresh water. 1256. Synaptura Fitzroiensis. De Vis. Proc. Linn. Soc, N. S. Wales. Vol., VII., p. 319. Fitzroy Eiver. 1257. Synaptura cinerea. De Vis. Proc. Linn. Soc. N. S. Wales. Vol. VIIL, p. 288. Moreton Bay. 1258. Plagusia notata. De Vis. Proc. Linn. Soc, N. S. Wales. Vol. VIIL, p. 288. Moreton Bay. Species. 799. Plagusia guttata. Macleay. Klunzinger thinks this is the Plagusia japoaica of Schlegel. 52 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, Genus. Lophorhombus. Macleay, Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 14. This is without doubt the genus Lophonectes of Gunther. Report ofZool. of Challenger Exp. Part VI., p. 28. Dr. Gunther's name has priority. 1259. Lophorhombus cristatus. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 14. Lophonectes gallus. Gunth. Report Zool. Chall. Part VI. p. 29. PI. XV, fig. B. Port Jackson. Dr. Gunther's name has pi-iority. Genus. L^eops. Gunth. Body oblong ; head small ; cleft of mouth very narrow, with the dentition much more developed on the blind side than on the coloured. Teeth villiform, in narrow bands ; palatine and vomerine teeth none. Dorsal fin commencing above the front margin of the eye. Scales small, thin, deciduous. Eyes on the left side. 1260. L^eops parviceps. Gunth. Report of Zool. Challenger Exp. Part VI., p. 29. PI. XV. fig. A. D. 104. A. 86. The height of the body is contained 2§ in the total length (without caudal), the length of the head 5 J. The snout is very short. The eye rather large ; its diameter being 3|- in the length of the head. A very narrow ridge, longitudinally grooved, separates the two eyes, the lower being conspicuously in advance of the upper. The mouth is directed upwards, and the maxillary of the left side extends scarcely below the anterior margin of the eye. The dorsal fin commences opposite to the front margin of the upper eye and is continued to the root of the caudal, the rays being of moderate length. Caudal rounded. The left pectoral rather longer than the light, and as long as the postorbital portion of the head. The rays of the left ventral are arranged in the N BY WILLIAM MACLEAY, F.L.S., &0. 53 same line as the anal, the right ventral being entirely on the tight side. The lateral line makes a very short semi-circular curve anteriorly, and is straight for the remainder of its course. The colour appears to have been uniform brown. Off Twofold Bay. (Gunther.) Genus. Cynoglossus. Ham. Buch. Eyes on the left side ; pectorals none, vertical fins confluent. Scales etenoid ; lateral line on the left side double or triple ; upper part of the snout produced backwards into a hook ; mouth unsymmetrical, rather narrow ; lips not fringed. Teeth minute, on the right side only. Gill-opening very narrow. Indian Seas. 1261. Cynoglossus quadrilineatus. Bleek. Atl. Ichth. Pleuron. p. 32, tab. 14, fig 3. Gunth. Cat. IV. p. 497. D. 102-112. A. 83-86. C. 10. V. 4. L. lat. 95. Two lateral lines on each side, separated in the middle by about fourteen longitudinal series of scales. Two nostrils, one between the eyes, the other below the lower angle of the lower eye. The upper eye somewhat in advance of the lower. Lips not fimbriated. The length of the snout is contained twice and two-thirds in that of the head. The rostral hook just covers the symphysis of the mandibles. The height of the body is somewhat less than one- fourth of the total length, the length of the head one-fifth. Uniform brownish ; fins yellowish ; a black spot on the operculum. Cleveland Bay. (Klunzinger.) Family. SILUKID^E. 1262. Cnidoglanis Mulleri. Klunz. Sitzb. der K. Akad. der Wissensch. 1879, p. 411. D. 1/5. Height of body 7 and length of head 6 in the total length. Snout a little projecting ; underlip thick and covered with warts, without fringe, not pendent. Side fringes on the angle not threadshaped ; the nasal barbel reaches a little beyond •54 SUPPLEMENT TO CATALOGUE OF THE PISHES OF AUSTRALIA, the head, but not to the dorsal fin ; the maxillary barbels are much shorter, only reaching just beyond the eye; the outer mandibulary barbels reach to the branchial aperture, the inner about half the distance. Five short canine teeth on each side of the lower jaw. 1st dorsal fin as high as the body and a little shorter than the head ; pectoral spine a little shorter than the dorsal. Colour uniform brownish. Allied to C. microcephalics, 15 Ctm. Port Darwin. (Klunzinger.) Family. HAPLOCHITONID^. Genus. Haplochiton. Jenyns. General habit of the trout, but completely naked. The dorsal fin occupies a position somewhat posterior to that of the ventrals. which are in the middle of the length of the body, and composed of seven rays. Adipose fin small ; caudal forked ; anal of inodei'ate length. The nostrils are somewhat remote from each other. Eyes of moderate size. Teeth small, curved, in a single series, in the upper and lower jaw and on the palatine bones. Tongue broad, with a series of curved teeth on each side. Gill-openings rather wide, the gill-membranes not attached to the isthmus ; the outer branchial arch with lanceolate gill-rakers. Pseudobranchia? well developed. Air-bladder simple, grown to the walls of the abdomen. Stomach thick and muscular ; pyloric appendages none. The urogenital organs of both sexes are produced into a cylindrical tube, which lies concealed in a groove before the anal fin. Tierra del Fuego and Falkland Islands. 12G3. Haplochiton Sealii. Johnston. Proc. Roy. Soc. Tasman., 1882, p. 128. The Derwent Smelt. B. G. D. 8-9. A. 19-20. V. 7. P. 9-12. Vert. 56-57. " Body naked. Total length 5-3 times length of head and nearly 10 times the height of the body. Head somewhat broad, depressed ; interorbital space wide. Teeth in a single series, small, hooked, on maxillary and mandible, minute on the palate. Eye relatively large, diameter equal to length of snout, which latter is contained BY WILLIAM MACLEAY, F.L S , &C. 5J5 in head 3 2 times. Maxillary extending to a vertical line drawn through centre of eye ; posterior end slightly enlarged, and curved downwards. Lower jaw slightly longer. Dorsal situated rather in advance of vent and behind ventral fin. Belly rounded. Adipose fin membranous, rudimentary, broadly deltoid. Body ornamented with extremely minute dots ; from the ventrals forward I minute dots form two pai'allel interrupted lines, which gradually approach and unite at an acute angle under the mandibles. Silvery band along sides. Length 1 to 2 inches. Upper Derwent River. Tasmania. Family. SCOPELID.L. 1264. Saurida ferox. Ramsay. Proc. Linn. Soc, N. S. Wales, Vol. VIIL, p. 177. Port Jackson. Family. GALAXID.E. 1265. Galaxias rostratus. Klunz. Archiv. fur Naturg., 1872, p. 41. R. br. 6. D. 11. A. 14. P. 14. V. 7. Height of body 8£ and length of head 5£ in the total. Body very slender ; forehead broad and flat. Jaws equal, each with a row of slightly hooked teeth, the same on the palate ; those on tongue in two rows. Eye shorter than the snout ; the maxillary reaches to below the middle of the eye. The dorsal fin commences at the beginning of the last third of the body, and a little in front of the anal fin. The free part of the tail is as long as the anal fin ; the caudal is slightly emarginate ; the ventrals are situated midway between the base of the caudal and the front margin of the eye ; the pectorals are of the same length as the ventrals and are much shorter than half the distance between the two fins. Colour uniform brownish-yellow, fins bright ; across the base of the tail a dark cross-band on spot. Length 13 Ctm. Murray River. (Klunzinger.) 56 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, 12G6. Galaxias Findlayi. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VIL, p. 107. Mount Kosciusko. 1267. Galaxias auratus. Johnston. Proc. Linn. Soc. Tasman, 1882, p. 131. " Lake Trout." . B. 9. D. 11-12. A. 14. P. 16. V. 1/7. " The height of the body is contained five times in the total length ; the length of head nearly four times. The head is very much depressed. Interorbital space wide, having three pairs of poi'es over each eye. About seventy distinct pores, mostly in. pairs, along usual course of lateral line. Head blackish. Body of a bright transparent golden hue. Spots very large, rounded and sometimes confluent above lateral line. No blackish bars across shoulder. Ventrals tipped with black ; base and tips of anal and dorsal blackish. Pectoral reaches half the distance from root of ventral. Total length 9f inches." Hah. Great Lake, alt. 4000 feet. Tasmania. 1268. Galaxias Weedoni. Johnston. Proc. Royal Soc, Tasman., 1882, p. 131. "Mersey Jolly-tail." D. 11. A. 14. P. 15. Body somewhat compressed. Length of head scarcely exceeding the depth of bochy, and contained four and a half times in the total length. Pectoral reaches half the distance to root of ventral. Head and body brownish black ; back and sides marbled with irregularly transverse wedged-shaped streaks, and bands of darker hue. Caudal bifurcate. Length 4 J inches." Mersey River, Tasmania. 1269. Galaxias Atkinsoni. Johnston. Proc. Boy. Soc, Tasman., 1882, p. 131. "Pieman Jolly-tail." B. 9. D. 11. P. 13. A. 14. V. 8. " Length 4^ times that of the head, and the latter is equal to 1| the height of the body. Diameter of eye equal to length of snout BY WILLIAJI JIACLEAY, F.L.S., &C. 57 and ^ of head. Pectoral reaches more than half the distance to root of ventral. The depth of caudal peduncle not half the length of distance between dorsal and caudal fins. Colour darkish brown, sides with 16 to 18 regular transverse bands of a deeper shade composed of microscopic dots, larger dots are distributed along the lines of vertebrse and ribs. Length 2£ inches. Pieman River, Tasmania. Family. SCOMBRESOCID^E. 1270. Belone Grceneri. Klunz. Sitzb. der K. Akad. der Wissensch. 1879, p. 414. D. 19-20. A. 20. Height of body 1J in the length of the pectoral fin. Head above with a shallow but distinct groove ; tongue rough ; length of head a little more than one-third of the total length without the caudal fin. In other respects this species is like B. robustus. Gunth. A slight keel of skin on the tail which is higher than broad ; posterior dorsal and anal rays low ; the lower margin of the maxillary only visible ; scales small, adhering, caudal fin forked. B. charan has the posterior dorsal and anal rays longer, and is also different in its dimensions and fin formula. B. liuroides has larger scales and larger head. The colour in this species is like the rest of the genus, Dr. Klunzinger thinks that this species is also quite distinct from B. gavealoides of Castelnau, but he complains that that species has been very inadequately described. 60 Ctm. Port Darwin. (Klunzinger.) Family. CLUPEID^E. 1271. Eugraulis Carpentaria. De Vis. Proc. Linn. Soc, N. S. Wales. Vol. VII., p. 320. Norman River. 1272. Engraulis heterolobus. Riipp. Gunth. Cat. VII. p. 392., Klunz. Archiv. furNaturg. 1872, p. 42. B. 12. D. 14. A. 17-18. L. lat. 42. 58 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, The height of the body is two elevenths of the total length, the length of the head one-fourth ; head not quite as long as deep. Snout pointed, much projecting below the lower jaw ; maxillary very finely toothed, rather pointed behind, extending somewhat beyond the mandibulary joint. Origin of the dorsal fin midway between the end of the snout and the root of the caudal fin. Anal commencing immediately behind the dorsal. Abdomen compressed in front of the ventrals, with several scutes. A well defined silvery band along the side. Cleveland Bay and Hobson's Bay. (Klunzinger.) 1273. Engraulis mystax. Bl. Schn. Gunth. Cat. VII., p. 397. Bleek. Atl. Ichth. Chip., p. 132- Tab. 3. Fig. 2. B. 12. D. 13-14. A. 34. L. lat. 42. The height of the body is contained 3J or 3£ in the total length (without caudal), the length of the head 4 times. Snout, short, obtuse, much projecting below the lower jaw. Teeth present in both jaws, minute. Maxillary much prolonged, extending to, or nearly to, the ventrals ; it has a short dilatation above the mandibular}' joint. Gill rakers not very fine, about 10 on the lower branch of the outer branchial arch, the longest as long as the eye. Origin of dorsal fin somewhat nearer to the end of the snout than the root of the caudal. Anal commencing shortly behind the last dorsal rays. Abdomen compressed, the spine scutes extending to the gill-opening. Sometimes a blackish spot across the nape down to the scapula. Queensland. (Klunzinger.) 1274. Engraulis Hamiltonii. Gray. Gunth. Cat. VII., 395. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. ^09. E. poovawali Cuv. Bleek. Atl. Clup. tab. 1, fig. 5. E. Grayi Kner. Voy. Nov. B. 13. D. 13. A. 36-40. L. lat. 47. The height of the body is contained 3| or 3f in the length (without caudal.) The length of the head 4| or 4^. Both jaws BY WILLIAM MACLEAY. F.L.S., &C. 5S with minute teeth ; the maxillary dilated above the mandibular; joint, its posterior tapering portion extends to or nearly to, the root of the pectoral fin. Origin of dorsal midway between the end of the snout and root of the caudal. Anal commencing immediately behind the last dorsal ray. Entire abdominal ridge serrated. Scapulary region with black venules. Gill-rakers rather strong, distant, 13 on the horizontal branch of outer branchial arch, the longest rather shorter than the eye. Lower Burdekin in Shoals. (Macleay.) 1275. Chatoessus elongatus. Macleay. Proc. Linn. Soc. N. S. Wales. Vol. VIIL, p. 209. Lagoons. Mary River. Species. 887. Chatoessus Erebi. Klunzinger regards C. erebi of Castelnau as identical with the above species, and C. Richardsoni Castelnau as the true C. erebi of Richardson. Family. MUR^ENTD^. 1276. Anguilla amboinexsis. Pet. Gunth. Cat. VIIL, p. 34. Origin of the dorsal fin twice as far distant from the pectoral fin as from the vent. The length of the head one third of the distance of the vent from the end of the snout. Angle of the mouth below the hind margin of the eye. Teeth small, in broad bands, that of the vomer rather narrower than that of the maxillary. Yellowish-brown, spotted with dark brown. Port Phillip. (Klunzinger.) 1277. Anguilla marginipinnis. Macleay. Proc. Linn. Soc. N. S. Wales, Vol. VIIL, p. 210. Lillesmere Lagoon, Burdekin River. 1278. Mur-enicbthys macropterus. Bleek. Atl. Ichth. Mur., p. 31, tab. VII , fig. 3. Gunth. Cat, VIIL, p 52. GO SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA. Origin of the dorsal fin nearer to the gill-opening than to the vent. Snout pointed, the greater part of the teeth biserial. The cleft of the mouth extends somewhat behind the eye. Length, 14 inches. Port Phillip. (Jvlunzinger.) Family. SYNGNATHID^E. 1279. Syngnathus cinctus. Ramsay. Proc. Linn. Soc. N. S. Wales, Vol. VII., p. III. Port Jackson, in 17 fathoms. 1230. Syngnathus superciliaris. Gunth. Report Zool. Exp., Challenger, part VI., p. D. 23. Osseous rings. 20 x 38. Snout as long as the postorbital part of head, with a median ridge above, terminating on the interorbital space, neck com- pressed into trenchant ridge ; operculum without keel and with fine radiating striae. Shields without spines ; lateral line passing into the lower caudal edge ; base of the dorsal fin not elevated, standing on three body and three caudal rings. Tail twice as long as the trunk. A very conspicuous filament above each eye. Pectoral and caudal fins well developed. Brownish-grey, with indistinct darker cross-brands, and finely marbled with darker and lighter spots ; snout and lower half of head with oblique vermicu- lated brown lines. Length, 3 to 6f inches. Port Jackson. (Gunth er.) 1281. Syngnathus caretta. Klunz. Sitzb. der K. Akad. der Wissensch. 1879, p. 419. & modestus Klunz. (nee. Gunth.) Archiv. fur Naturg., XXXVIIL, 1872. D. 24. Osseous rings, 17 x 42-44. Head 81-9 in the length; snout 2\ in length of head; trunk half the total length. Operculum with a short longitudinal ridge in front only. Two nape shields witli a longitudinal crest in middle. The lateral line is distinct as far as the anal shield. On the caudal shields it is either wanting or indistinct and interrupted. The dorsal fin commences on the anterior part of BY WILLIAM MACLEAY, F.L.S., &C. Gl the anal ring ; pectoral and caudal fins distinct, anal rudimentary. Body anteriorly a little higher than broad, nearly square. Colour brownish on the back, with lighter shield like transverse marks or bands at varying distances, and about 12 in number. 10 Ctms. Port Phillip. (Klunzinger.) 1282. SOLEITOGNATHUS FASCIATUS. Gimth. Report Chall. Exp. Zool. Part VI., p. 30, pi. XIV., fig. B. D. 41. Osseous rings, 27 x 55. This species is most closely allied to Solenognathus spinosissimus, having the same rough and spiny scutes, but the forehead is some- what broader, the dorsal longer and composed of more numerous rays, and the back of the trunk ornamented with seven narrow blackish cross-bars. Also the prseanal region is blackish. Length of specimen, 11 inches, (tail h\ inches. Twofold Bay. 120 fathoms. (Gunther.) Family. GYMNODONTES. 1283. Tetrodon reticularis. Bl. Schn. Gunth. Cat. VIII., p. 296. T. testudineus Bleek. Atl. Gymnod, p. 71, pi. 8, fig. 3. Very small spines cover the whole body from the nostrils to the root of the caudal fin ; those on the abdomen with two, three, or four roots. Snout short and obtuse, about one-third of the length of the head, and two-thirds of the width of the broad and flat interorbital space. Length of the caudal fin ecpxal to its distance from the front margin of the dorsal. Abdomen with rather numerous brown or black longitudinal bands, obliquely ascending over the cheeks to the upper part of the head, and passing on the side into a brown network, the meshes enclosing round whitish spots. On the back the brown is the ground colour, with round whitish spots. Caudal fin with round yellowish spots, separated by a blackish network. Vert. 8/10. Lower Burdekin. Salt water. (Macleay.) G2 SUPPLEMENT TO CATALOGUE OP THE FISHES OF AUSTRALIA, Family. CARCHARID^. 1284. Carcharias crenidens. Klunz. Sitzb. der K. Akad. der Wissensch. 1879, p. 426. Taf. VIII., fig. 3 Of the subgenus Scoliodon. Teeth in both jaws serrated on the outer edge of the base, oblique, and without middle tooth in the lower jaw ; no serration on the inner margin. The teeth in the upper jaw 12/1/12, in the lower 12/12. The fold of the upper lip is very distinct, therein differing from C. acutus, and is a little longer than the under one. The fold of the upper lip occupies J of the half of the lip, that of the lower 1/4 of the half of the lower lip. Snout long, obliquely obtuse in front, the distance between the outer angles of the nostrils is much greater than that between the nostrils and the snout ; the length of the snout from the anterior margin of the mouth is equal to the distance of the eye from the anterior gill-opening. Pores on the head as in C. acutus. The length of the base of the anal fin is equal to half its distance from the ventral. Colour as in C acutus, pectorals whitish margined behind ; the back of the caudal dark. 60 Ctm. Queensland. (Klunzinger.) Family. LAMNID^E. Genus. Selache. Cuv. The first dorsal fin opposite to the space between the pectoral and ventral fins, without spine ; the second and the anal fin very small ; a pit at the root of the caudal fin, which is provided with a lower lobe. Side of the tail with a keel. No memtrana nictitans. A very small spiracle above the angle of the mouth. Gill-openings exti-emely wide. Teeth very small, numerous, conical, without sei-rature or lateral cusps. Arctic Regions. 1285. Selache maxima. Gunn. Gunth. Cat. VIII., p. 394. Basking Shark of Northern Europe, This is the only species known of Selache, so that the generic characters sufficiently describe the species. It has hitherto been BY WILLIAM MACLEAY, F.L.S., itC. 63 believed to inhabit only the Arctic Regions, but the recent discovery of one by Professor MacCoy on the Coast of Victoi'ia, seeing to point to the conclusion that it is also an inhabitant of Antarctic Seas. The Victorian specimen caught at Portland Bay, measured over 30 feet in length and 20_feet in girth. Family. SCYLLID^E. 1286. Crossorhinus ornatus. De Vis. Proc. Linn. Soc., N. S. Wales. Vol VIII., p. 289. Moreton Bay. Family. RAILD^E. 1287. Raja australis. Macleay. Proc. Linn. Soc, N. S. Wales. Vol. VIII., p. 461. Outside Port Jackson in 50 fathoms. 1288. Raja nitida. Gunth. Report Chall. Exp. Zool. Part VI, p. 27. PL XIV., fig. A. Angle of snout obtuse, with a very thin median papillary pro- jection. Width of interorbital space a little less than the length of the orbit, and distance between the outer margins of the nostrils, less than their distance from the extremity of the snout. Teeth with very small points, almost obtuse. Outer pectoral margin obtusely rounded, the greatest width of disk being equal to the distance of the snout from the extremity of the ventral. All the upper parts covered with minute asperities, one or two curved spines in front, and behind the orbit, one in the middle of the back, and a series along the median line of the tail. Above light brown marbled with dark brown blotches which are orna- mented with small round yellowish ocelli. Twofold Bay, 120 fathoms. 1289. Raja dentata. Klunz. Archiv. fur Naturg., XXX VIII., 1872. Breadth 1^ in the total length. Length of disk (to the end of the base of the pectoral fins) 1^ of the breadth of the disk. Tail nearly as long as the disk, which is twelve times as long as the 64 SUPPLEMENT TO CATALOGUE OF THE FISHES OF AUSTRALIA, eye. Disk irregular, rhombic, its length not much less than its breadth. The snout is obtuse and not projecting. The front side of the pectoral fins rectilinear, the posterior slightly curved with rounded sides and backward angle. Eyes moderate, their longi- tudinal diameter equal to the breadth of the forehead. This last is concave. The snout cartilage is narrow, expanding towards the forehead. The distance between the nostrils is the same as their distance from the end of the snout. The back of the disk is every- where covered with minute spines, with stronger ones disposed as follows : — One row along the supercilliary ridges in a curve, one row in the middle line of the back, extending to the tail where they are arranged in alternate irregular double rows. There are also large spines on the side of the tail, especially at the base ; there is also a group of smaller spines on the cartilage of the snout. The teeth are in 42 longitudinal rows and are not acute. The ventral fins are long, their outer margin lobed, the front part with projecting points. Tail very depressed, a slight fold along the side, and compressed at the extremity, no distinct caudal fin. The two dorsal fins are close together, close to the tail, equal in size and rounded ; the shoi't space between these two fins bears a few spines. Colour grey, underneath white. 50 Ctm. Port Phillip. (Klunzinger.) 1290. Trygon sephen. Forsk. Gunth. Cat. VIIL, p. 482. Macl. Proc. Linn. Soc, N. S. Wales, Vol. VIIL, p. 212. Tail with a broad cutaneous fold below, but without one above, about thrice as long as the disk. Disk rhombic, with obtuse angles. The upper parts densely covered with flat scale-like tubercles ; several large globular tubercles in the median line of the scapulary l'egion. Coloration uniform. Lower Burdekin. Salt water. (Macleay.) 1291. T^eniura Mortoni. Macleay. Proc. Linn. Soc, N. S. Wales, Vol. VIIL, p. 212. Lower Burdekin. Salt water. 65 On some new Batrachians from Queensland. By Charles W. De Vis, M.A. LlMNODYNASTES LINEATUS. Habit rather slender, but with powerful hind limbs. Tongue oval, with its free hind edge scarcely eruarginate. The line of the vomerine teeth extends somewhat beyond the choanal, and is but slightly interrupted ; each half is dilated in the middle, has its anterior edge convex, and its posterior rather concave. The choanee are small and obliquely elliptical. The head is as broad, or nearly as broad as long. The snout is rounded, longer than the orbit, and as long as or longer than the interorbit. The nostrils are equally distant from the orbit and tip of the snout. The loreal region is concave, the tympanum indistinct. The first finger is shorter than the second ; the second in the female is broadly fringed. There are three metacarpal and one metatarsal tubercles, the latter small and blunt. On protraction of the hind limb the ankle reaches the front edge of the orbit. The skin is entirely smooth. Measurements : — Total length 18 lines Osseous interorbit .. 2-3 lines Length of head 8 ,, Hind limb 16 ,, Breadth of head 7|-8 „ Foot 9 „ Snout 3 „ Forelimb 10* „ Orbit 2| „ The ground colour is olive green to olive brown. A black longitudinal line commencing in a spatulate marking on the interorbit runs on each side of a narrow vertebral line of the ground colour. External to this, a broad black band runs along the side of the back. A third proceeds from the tip of the snout over the canthus rostralis and the eye to the shoulder, or is continued on to the body, where it breaks up into spots. Flanks and limbs on their front and back surfaces mottled with chestnut brown. Lower surface of thighs rufous, chin and throat mottled with brown. A black spot on the upper lip. 66 ON SOME NEW BATRACHIANS FROM QUEENSLAND, Four specimens collected at Mackay, by Mr. H. Ling Roth. Approaching near to L. Pei'onii, the present is sufficiently distinct from that species. Its chief differences are a shorter hind limb and a well-defined continuity in its dorsal stripes. LlMNODYNASTES OLIVACEUS. Habit stout, with short strong hind limit. Tongue orbicular, with the free hind edge slightly nicked. Vomerine teeth in an interrupted sei'ies, each half slightly curved, extending a little beyond the choanss, which are round. Snout rather longer than the orbit, which is longer than the bony interorbit. Nostril ecpially distant from the eye and tip of the snout. Tympanum invisible. Canthus rostralis rounded. Loreal region shelving, rather concave. Three metacarpal and two metatarsal tubercles ; the inner metatarsal small, the outer long and low. On protraction of the hind limb, the ankle reaches the hinder angle of the eye. Skin of back and upper side of limbs covered with strong tubercules. Measurements : — Total length 18 lines Osseous interorbit 2 lines Length of head 1\ „ Hind limb to ankle... 14| ,, Breadth of head 7£ „ Foot 9 „ Snout 3-1 „ Forelimb 9 ,, Orbit 3 „ Colour olive green, with yellowish bars on the lips and snout. One example collected at Mackay by Mr. H. Ling Roth. Hyla Rothii. Habit slender, with a slender hind limb. Tongue oval, with its free hind edge rather deeply emarginate. Vomerine teeth in two small groups between the choanee. Choanse rather large, angular. Head small. Snout subacute, longer than orbit or interorbit — the latter ecpial. Nostril much nearer the tip of the snout than to the eye. Loreal region shelving, rather concave. Tympanum distinct, two-thirds of orbit. Fingers half-webbed, but fringed to BY CHARLES W. DE VIS, M.A. G7 the disks ; disks about two-thirds of tympanum. Toes entirely webbed, with small disks. On protraction of the hind foot, the ankle reaches between the eye and the nostril. No distinct tarsal fold. A faint fold over the wrist. Measurements : — Total length . 20 lines Osseous interorbit. .. 3 lines Length of head 1\ „ Hind limb to ankle... 18J „ Breadth G£ „ Foot 9 „ Snout 4 ,, Fore limb, entire 10.', ,, Orbit 3 „ Colour variable, lead grey, olive or reddish brown, uniform or mottled with darker. In one example, a faint trace of a dark line on each side the back, anjd a fine dark line from the nostril to the eye, curving down to the upper lip. In all the axil is black ; the groins have large black spots which may run together into a line between the groin and the axil. On the foreside of the thigh a long irregular black stripe breaking up into spots distad. Pos- teriorly, a similar black line enclosing more or less completely one or two large yellow spots Lower surface of thigh purplish-red. Generally a black crescentic band across the wrist. Four specimens collected at Mackay by Mr. Ling Roth. Occasional Notes on Plants Indigenous in the immediate neighbourhood of sydney. no. 6. By E. H AVI LAND. This paper is the result of observations and notes that I have made, from time to time during the past six months, on some species of the genus Darwinia. That most common in the immediate neigh- bourhood of Sydney is D. fascicularis. I have, however, found one or two plants of D. taxifolia. The two species closely resemble each other ; the leaves of D. taxifolia being a little more fiatt than in D. fascicularis ; and the flowers in each head fewer. Its G8 NOTES ON PLANTS INDIGENOUS TO SYDNEY, specific name, taxifolia, was given to it by Allan Cunningham. Schauer, however, described it as D. laxifolia ; and seems to have considered the name taxifolia a misprint ; for Bentham adds a note to his description in the " Flora Australiensis" (Vol. 3, p. 12), in which he says, " Schauer was mistaken in supposing that Allan Cunningham's specific name of taxifolia was a misprint ; it was intended to allude to the pecular bifarious arrangement of the leaves, in luxurious branches." In the third volume of the " Flora Australiensis," in which the genus Darvrinia is described, only twenty-three species are enumerated. Von Mueller, however, in his census recently published, gives thirty-seven species. It must not be forgotten that most of the volumes of the "Flora Australiensis " were published many years ago. This third volume, for instance, eighteen years. Perhaps then, I may be allowed to refer here to the great debt of gratitude that I think is owing by all botanists, but especially by Australian botanists, to Baron von Mueller, by whose untiring energy they have been kept acquainted with all discoveries of new genera and species, since the publication of that work. Darwinia fascicularis, of which species I speak more particularly in this paper, is very common about our coast line, being especially plentiful between Coogee and Botany. It belongs to the order Myrtacece ; and is a low-lying, half decumbent shrub ; having its leaves heath-like, crowded and nearly terete ; its infloresence in terminal heads of ten to twenty flowers ; presenting a rather curious appearance by having, often on the same head, some of its flowers white, while the others are red ; the red colour, however, extends only to the limb of the corolla, the tube, in all cases, being white. If, as suggested in my last paper, the corolla is slit open, and spi'ead out by small pins on a flat piece of cork, its five pointed lobes, with its ten stamens and shining black, gobular anthers, alternating with ten staminodia, which are often tipped with crimson rudimentary anthers, give it, especially under a low microscopic power, a very beautiful and gem-like appearance. The genus, even if not otherwise interesting, will always be so by bringing to memory the name of one of the most illustrious BY E. HAVILAND. G'J naturalists of our time ; but indeed, even confining my remarks to Darivinia fascicularis, I may say that it is a plant possessing great interest to all engaged in the study of vegetable life. In my last paper I brought under your notice a plant, Myrsine variabilis, which appeared to me to have its flowers always closed to ensure self-fertilization. Here, -however, I speak of a plant whose flowers, or nearly all of them, appears to be always closed to prevent it. There is, however, this difference between them, that in the former case, both anthers and stigma are shut in the corolla together ; while in the latter, the anthers are shut in, while the stigma is shut out, so that there can be no communication between them. Here and there, however, in D. fascicularis, an open flower is found without this separation of the fertilizing organs ; but I think I am within bounds when I say that of a hundred of its flowers, ninety-five never open. T do not make this assertion from the inspection of a few flowers, but as the result of long and cai"eful watching. Indeed, it was not until I had been studying the plant for some time that I could find any open flowers ; and so under the impression that all were closed, having the anthers and stigma completely separated, I was at a loss to conceive how the plant was fertilized, Thinking that perhaps the corolla opened either during very bright sunlight, or perhaps as jEnothera, and many other flowers, rn the early evening or at night, I have during this summer marked many flowers, and have watched them at all hours during both bright and cloudy days, and have also made special visits to Coogee at night for that purpose ; but in no instance have I found flowers open except in the very few cases where they were so from the first. In one instance I marked a branch bearing three heads, consisting in all of forty-two flowers. Of these none were open ; none of the styles projected more than a quarter of an inch beyond the closed corolla, shewing that the flowers were but little beyond the condition of buds. In four days I again visited this plant ; none of the flowers were open, but the styles all projected more than an inch beyond the corolla. Nearly all the stigmas were mature and ready to i-eceive pollen. In a week I made another inspection, finding the flowers still all 70 NOTES ON PLA.NTS INDIGENOUS TO SYDNEY, closed. Of the three heads, one, comprising fourteen flowers, had pollen of on four the stigmas. A second, having twelve flowers, had no pollen on the stigmas. The third, which contained sixteen flowers at first, but now only thirteen, three having withered, had pollen on seven of the stigmas. I think the fact that, in the whole of these flowers, the anthers were closely shut up within the corollas, while the stigmas were outside at some distance from them, and that no communication could possibly take place between them ; proves, beyond doubt, that they were cross-fertilized ; or that, at least, the pollen on the stigmas came from some other flowers. It also proves, I think, that if my estimate of the proportion of closed and open flowers is correct, ninety-five per oent. of them are entirely dependent on the remaining five per cent, for their fertilization. While sitting at a little distance from this plant, trying to think out how it could have been fertilized — for up to that time I had seen no open flowers — I noticed two or three small bees hovering about one particular part of it. If I frightened them away they invai'iably returned to the same place ; and, upon searching there, I found a head of ten flowers, three of which were open ; the anthers were fully exposed, and the pollen exuding from them. I revisited it several times, but, from first to last, the same three flowers only had opened. The stigma is very small, being merely the point of the style ; but there is one feature in the plant which I consider of great importance. Immediately below the stigma is a ring of stiff hair- like glands, which secrete an adhesive fluid copiously. This secretion is greater in the young than in the mature flower. Indeed, if a bud is opened, it will be found so copious that a broad baud or ligature is formed of it, extending from the style across to the inner surface of the corolla. As the flower approaches maturity, although the secretion is not so copious, it collects in considerable quantity, forming a globule close under the stigma ; and not only often creeping up to it, but running clown the style In the course of time it dries into a smaller mass. BY E. HAVILAXD. 71 Considering that only about five per cent, of the flowers open, and consequently that that proportion of the pollen only is avail- able for the fertilization of the plant, and that the anthers do not open by slits, as is most usual ; but by two very minute pores, thus giving out the pollen grudgingly ; that the pollen, even in the anther, is by no means abundant, but rather the reverse; taking, too, into consideration that each flower produces but one seed, one cannot help feeling surprise that the plant is so abundant. I think, however, this may be accounted for to a great extent, by the presence of the secretion of which [ have spoken. The fact of its being more copious in the younger flowers while the styles are comparatively short, and the secreting glands are near the surface of the head of flowers, renders it almost impossible for an insect to crawl about the stage, formed by the compact head, without becoming so smeared with it, that on visiting an open flower much of whatever pollen might be exposed, would adhere to it, and be carried away by it ; and for the same reason upon its visiting the mature stigmas of the closed flowers, a little only of the pollen, but cpiite sufficient, since there is only one ovule to be fertilised, would be left on each ; the greater part remaining adhering to the insect, who would carry it from one flower to another. Thus it is not unlikely that by the pollen obtained by one visit to an open flower, very many of the closed ones would be fertilised. Studies ox the Elasjiobranch Skeleton. By "William A. Haswell, M.A., B.Sc. [Plates I. and II.] In his well-known memoirs " Das Kopfskelet der Selachier " and "Die Brnst-Flossen der Fische,"f Gegenbaur has treated very exhaustively of the structure and homologies of these part s * Untersuchungen zur vergleichenden Anatomie der Wirbelthiere. Heft- 3. t Op. cit. Heft. 2. 72 STUDIES ON THE ELASMOBRANCH SKELETON, of the skeleton in the Selachoidei. There was an absence, however, in the material at his disposal, rich though it was, of certain southern forms of some little importance ; and a study of some of those has enabled me to observe several points of some theoretical interest. The following is the list of the species examined : — Heptauchus indicus Complete skeleton. Heterodontus (Cestracion) Phillipi ... do. Carcbarodon Rondeletii do. Crossorhinus barbatus do. Cheiloscyllium furvum do. Squatina angel us do. Pristiophorus cirratus do. Trygonorhina fasciata do. Trygon pastinaca do. Urolophus testaceus do. Hypnos subniger do. Galeus canis dried skull. Scy Ilium stellarius do. Lamna cornubica do. Scymnus circaeensis do. Mustelus laevis do. Zygaena malleus do. The skeletons of the Australian species were all examined in the fresh state, and the drawings made from them (with the aid of the camera and sometimes of photographs), while in that state or after preservation in glycerine jelly after Prof. T. J. Parker's method, so that little or no distortion or alteration had taken place. One of the principal objects which I have had in view has been to ascertain how far a comparison of all parts of the skeleton would bear out the deductions as to the affinities of the various groups, based by Hasse* on the structure of the vertebra?; and I have added at the close of the paper a synopsis of the anatomical characters of the skeleton in the principal sub-divisions, showing how far this has been carried out. * Morphologisches Jahrbuch, II., III., IV., andSupp. to IV. BY WILLIAM A. HASWELL, M.A., B.SC. 73 The following is a short general summary of the leading points in the skeletal anatomy of the Plagiostomata. The vertebral column of the Plagiostomata varies considerably in the degree to which the vertebra? become marked off from one another, and the embryonic tissue becomes ossified. In some ( Notidanus), no ossification takes place in the centra, and the segments are not very clearly separated from one another. In others ( Spinacidce, Lcemargidm and Echinorhinidce), each centrum presents a double osseous cone with the apices meeting in the middle and the cavities of the cones turned towards the anterior and posterior faces of the vertebra.* In the greater number of Sharks there is added to this double cone a series of osseous rays traversing the cartilaginous zone which forms the outer layer of the centrum. In one case only (Squatina) the rays are replaced by a series of concentric lamella? surrounding the double osseous cone. In some sharks (Notidanus for example), each vertebra in the caudal region bears two neural arches. In the Rays ossification of the vertebral column is more perfect than in the Sharks, and the anterior portion of the spinal column becomes fused into a continuous bony and cartilaginous mass. In all the caudal vertebra? ai*e distinguishable by the presence of in- ferior arches enclosing the caudal vessels. The first vertebra has its anterior surface modified for articulation with the occipital region of the cranium. In Hexanchus, in which the separation between adjacent vertebra? is very imperfect, the cartilage of the first vertebra is perfectly continuous with the cartilage of the cranium. In most other Selachii, however, the first vertebra developes lateral articular processes which articulate with the apposed surfaces of the occipital regiou of the skull. These lateral articu- lations are more markedly developed in the Rays, in which the median prolongation of the centrum of the first vertebra? fits into a deep excavation in the basis cranii, its apex being connected with the latter by a mesial ligament containing the rudimentary * This structure seems first to have been noticed by Home : See " On the nature of the intervertebral substances in Fish and Quadrupeds," Phil. Trans., 1809, pp. 177-184. 74 STUDIES ON THE ELASMOBRANCII SKELETON, prolongation forwards of the notochorcl, while its sides articulate with the occipital condyles. In the caudal region of Sharks the haemal spines become specially produced to afford support to the ventral half of the broad caudal fin ; closely related to the dorsal surface of the vertebrae in this region, but not continuous with the neural arches and supporting the dorsal half of the fin are a series of cartilages which, though resembling produced neural spines, are not continuous with the neural arches, and do not agree in number with the latter ; and in the trunk the dorsal and anal fins possess cartilaginous supports which sometimes present the appearance of modified neural and haemal spines. Frecpiently> however, the skeleton supporting these unpaired fins is entirely unconnected with the vertebral column, and, though in some cases the correspondence in position of its elements with the segments of the vertebral column seems to indicate some develop- mental relationship with the latter, in others, the skeleton of the fin becomes so modified by the formation of plate-like basal cartilages that this apparent correspondence is no longer traceable. The cranium of the Plagiostomata is formed of an undivided mass of cartilage, strengthened in many cases by the deposition of superficial layers of bony matter. It consists, in essence, of a cartilaginous case into the sides of which are incorporated the cavities or capsules that serve to protect the three pairs of organs of special sense, the ear, the eye, and the nose ; in the walls of which are apertures for the egress of the cerebral nerves ; and from which project certain processes which serve for the attach- ment of muscles or for connection with the anterior visceral arches. In the middle line behind is the aperture of the foramen magnum, the plane of which is usually inclined from below and behind upwards and forwards ; its lower lip is deeply excavated in the Rays for the reception of the mesial process of the first vertebra ; and on either side of this is one of the condylar surfaces which are articulated with the lateral articular processes of the first vertebra. In some sharks ( Notidanidce), the occipital region presents certain characteristics which assimilate it to the vertebral column ; in the middle above is a ridge seeming to prolong BY WILLIAM A. HASWELL, M.A., B.SC. 75 rorwards the line of the dorsal spines ; on each side is another ridge apparently continuous with the transverse processes, and a row of small foramina (through which pass divisions of the vagus nerve), which seem to continue forwards the row of spinal nerve-foramina. In a few other sharks ( Spinacidcu) these peculiarities are traceable in a less decided form ; but in the majority the mesial and lateral occipital ric'ges disappear. In front of the occipital is the auditory region of the skull, in which are contained the various divisions of the membranous labyrinth, and with which articulate laterally the hyo-mandibular cartilages. In the lower forms among the Plagiostomes the surface of the auditory region takes its form to some extent from that of the enclosed parts of the auditory apparatus, and elevations marking the position of the anterior and posterior semi-circular canals and of the vestibule are very prominent on the surface ; in higher forms these elevations become less marked, and in some exceptional instances they may become so obscured as to be barely traceable. On the upper surface of this segment of the skull are the two small apertures of the aqueductus vestibuli ; in the Sharks these two apertures are closely approximated to one another, and are situated at the bottom of a common pit or groove — the parietal groove. In the Rays, on the other hand, the two apertures are separated from one another by a distinct interval and do not lie in any common groove. The articular surface for the hyo-mandibular in the lateral wall of the auditory region varies greatly in its form and position. In form it varies from a simple concavity to a complex articular surface, sometimes divided into two parts ; it may be excavated on the lateral wall of the auditory region, or may be borne out from the general surface on prominent processes of the postero-lateral region of the cranium. In the Rays it is placed nearer the, base of the cranium than in the Sharks, and is more elongated antero- posteriorly. Behind it in the Rays is sometimes a small articular surface for the first branchial arch. In front of the auditory region is the orbital region, which presents on either side a deep concavity for the reception of the eye. 76 STUDIES ON THE ELASMOBRANCH SKELETON, In most Sharks the orbital cavity is bounded below by a plate of cartilage— the basilar plate ; but this is absent in all the Rays. It is frequently bounded in front and behind by prse- and post-orbital processes ; and its wall is perforated by apertures for the egress of the facial, trigeminal, abducent and oculo-motor nerves. A shallow groove passing forwards from the aperture for the trigeminal marks the coui'se of the ophthalmic branch of that nerve, and a series of foramina in the roof indicate the points at which the supra-orbital branches of the same nerve penetrate towai'ds the roof of the skull. In front near the upper border of the orbit is a canal or notch by which the ophthalmic nerve reaches the upper surface of the skull ; and in front of the orbit is a canal or notch (the ethmoidal canal or notch), by which it again passes downwards towards the lower lateral region of the olfactory capsule. In front of the orbits ai*e the olfactory capsules, which are more or less completely enclosed in cartilage, and are usually solid^ connected with the rest of the cranium. Related to the olfactory aperture is a small cartilage, the olfactory cartilage usually of the form of an incomplete ring. Between the nasal capsules the mesial portion of the skull is usually produced forwards into a longer or shorter rostrum, which may be single and contain a canal continuous with the cranial cavity, or may be composed of three solid bars of cartilage, a mesial and two lateral, which coalesce anteriorly. Directly or indirectly related to the skull are the palato-quadrate, Meckelian> hyoid and branchial arches. At the sides of the gape are the labial cartilages, of which there are usually two pairs above and one below. In the Rays labial cartilages, as a rule, are absent. The upper and lower jaws of the Elasmobranchii consist of the palato-quadrate and Meckelian cartilages respectively, the sub- stance of the cartilage being usually deeply impregnated with osseous matter. The palato-quadrate is distinguishable in the Sharks into an anterior, palatine, and a posterior, quadrate, portion. It presents in Notidanus a process for articulation with the post-orbital process. In the Notidanidce the palatine cartilages BY WILLIAM A. HASWELL, M.A., B.SC. 77 of opposite sides are widely separated from one another by an interval occupied by ligamentous fibres, but bearing teeth. The two halves are more closely approximated in other Sharks ; in some fCestracion, Scymnus) they are very intimately connected. In the Rays the palatine and quadrate portions are usually not well marked off from one another, and the two halves are intimately united together in the middle line. In the Sharks a palatine process is developed for articulation with the basis cranii, but this is absent in the Rays. The articulation between the palato-quadrate and lower jaw may be single, but, more usually, is divisible into two parts. In most Sharks the two halves of the lower jaw, or Meckel's cartilage, ai*e freely movable on one another, Cestracion being the most important exception ; in the Rays the movability is much less than in the Sharks, and the two rami may be united into a rigid bar. In the simplest arrangement to be observed in the Elasmo- branchii, the upper elements of the hyoid arch are similar in function and in relation to the arch to those of the succeeding branchial arches. They serve, that is to say, solely to suspend the ventral portion of the arch, and the union with the side of the cranium is slight and unimportant. In a further stage, such as is represented in Cestracion, these elements become a little more important and come into relation, slightly at first, with the palato- quadrate cartilage and lower jaw, which they help to suspend, still, however, being mainly related to the hyoicl ; in a yet more advanced stage (most Sharks) the cartilage becomes thicker and longer, its articulation with the skull becomes more complete, and by its distal extremity, which develops a special mandibular process, it is mainly related to the palato-quadrate and mandible, the relation to the hyoid having now become a subsidiary one ; the epi-hyal has now become a hyo-mandibular. In a further stage (Rays) the hyoid undergoes a degeneration, loses its distinctness from the branchial arches, and is attached to the base of the hyo- mandibular, or is no longer directly related to it, but articulates separately with the side wall of the cranium. Finally (as regards 78 STUDIES Oi> THE ELASMOBR.i.NCH SKELETON, this degeneration), in Hypnos and Trygonorhina the hyoid, now- become quite similar to the succeeding arches, is connected with the skull only through the epibranchial of the first branchial arch. Related to the hyo-mandibular is the spiracular cartilage, a thin usually four-cornered plate supporting the wall of the spiracle. The lower or distal portion of the hyoid arch consists of two lateral pieces on each side, and of a mesial cartilage or copula. The lateral pieces (as well as the hyomandibular) may bear rays similar to those of the branchial arches ; the mesial piece may be a broad plate or a narrow band of cartilage, or, as, in many Batoidei, may become altogether aborted. The internal branchial arches, which support the gill-pouches, are always five in number, except in Hexanchus, which has six, and Heptanchus which has seven. Each branchial arch, when typically developed, consists of a dorsal basal cartilage usually thin and leaf-like, and lying free close to the ventral aspect of the spinal column, sometimes styliform and articulating with the spinal column by a distinct joint (some Rays) ; of two mesial cartilages, a dorsal and a ventral, usually with deep grooves on their inner surface for the insertion of muscle ; of a copulare, and of a mesial ventral copula. In most, however, the copulpe become greatly reduced and may form a single basibranchial plate as in the Rays ; in Myllobatis and Trygon the copularia are likewise amalgamated with this basal-plate. The fifth arch has no copulare and no basal — its dorsal mesial articulating with the basal of the fourth: very often it is connected by articulation with the pectoral arch. The outer branchial arches, which are a series of cartilages bounding the branchial apertures and situated at the extremity of the branchial rays, are more rudimentary in Hexanchus and Heptanchus than in other Sharks ; they are best developed in Cestracion. They are absent in the Rays, though Gegenbaur found rudiments of them in Rhynchobatus and Trygon. The -pectoral arch is a stout cartilage, the lateral portions of which are curved backwards and inwards towards the vertebral column, with which they may articulate (Rays). The ventral BY WILLIAM A. HASWELL, M.A., B.SC. 79 portion of the arch is divided in the middle line in Sharks, (except Squatina and Heterodontus), by a mesial more flexible region which permits of a good deal of motion of the two halves upon one another ; but in the Rays the two halves are quite continuous with one another, the ventral portion of the arch forming "(except in Toledo), a rigid bar. Borne on the lateral portions of the arch towards its ventral aspect are the articular surfaces for the pectoral fins. Of these there are usually three, often placed in a horizontal line. Near the articular surfaces are the foramina for the transmission of the brachial nerves. The skeleton of the fin proper consists, when typically developed, of three basal cartilages — the propterygiwni, mesopterygium and metapterygium — and of a number of rays. In some Sharks (Heterodontus) the propterygium is absent, and in Scymnus the mesopterygium also ; in Rays the mesopterygium is always small, and some of the radial cartilages may articulate with the shorter-girdle directly, while the propterygium and metapterygium are greatly elongated. In Sharks the pectoral fins are of moderate extent and do not ai'ticulate with the cranium : in Rays, on the other hand, they are greatly expanded, extend far forwards as well as backwards, frequently completely encircling the head, and the propterygium is, except in the Torpedinidce, connected with the olfactory region of the skull, through the intermediation of an ant-orbital cartilage. The pelvic arch is a straight or slightly curved bar of cartilage, with the outer extremities of which the pelvic fins are articulated. Usually it is perforated by two nerve-foramina on each side, and may develope longer or shorter processes or cornua in front of and behind the articular surface. Each pelvic fin contains usually only two basal cartilages, the hinder being much the more important, and having the greater number of the rays articulated to its outer border ; connected with its distal extremity are the cartilages which form the skeleton of the clasper of the male. The structure of the fins of the Elasmobranchii has been minutely studied in connection with the subject of the origin and nature of limbs. A detailed knowledge of the anatomv of these fishes seems 80 STUDIES ON THE ELASMOBRANCH SKELETON, first to have been brought to bear on this question by Gegenbaur,* who came to the conclusion that the primitive limb-skeleton or Archipterygium resembled generally that of Ceratodus.j From this primitive form he traced the various modifications of the fiu of fishes and the limbs of the higher vertebrates. The Elasmobranch fin, with which we are immediately concerned, he regards as having been developed from the Archipterygium by the suppression of the post-axial series of fin-rays — the metapterygium representing the axis of the archipterygium, and the rnesopterygium and propterygium, together with the rays connected with them, having been derived from certain rays which he supposes to have been directly connected with the shoulder-girdle in the primitive fin. The archipterygium itself he regards as having been developed from a branchial arch and its connected rays. A similar view of the relations of the Elasmo- branch fin to that of Ceratodus and the Crossopterygian Ganoids was embraced by Professor Huxley, and maintained by him as late as 1876, J: but Huxley regarded the axis of the archipterygium as being represented by the mesopterygium, not the metapterygium, and does not give his adherence to the theory that the limbs are modified branchial arches. Balfour § has shown more recently (1878) that the paired fins of Scylliuiyi originate in two pairs of lateral ridges of epiblast, the embryonic limbs of each side being connected for a time by a low continuous ridge, which, however, soon disappears. In the messoblast subsequently growing into these folds of epiblast is developed a longitudinal bar of cartilage. The outer side of this is connected with a plate which extends into the fin and becomes segmented to form a series of parallel rays situated at right angles to the longitudinal bar. In front this longitudinal bar is continuous with the limb-arch. From these observations has been * Grundriss der Versrieichenden Anatornie. t See Giinther, Description of Ceratodus, Phil. Trans.. 1871. I On Ceratodus Forsteri, with Observations on the Classification of Fishes, P.Z.S., ISfG, pp. 24-59. § Monograph on the Development of Elasmobranch Fishes, pp. 101-104 ; Comparative Embryology, Vol. II., p. 49, (1881.) BY WILLIAM A. HASWELL, M.A., B.SC. 81 deduced the theory that in their simplest form the paired fins of fishes are simply continuous lateral folds similar in their derivation to the unpaired fins, the continuous fold of each side becoming subsequently differentiated into the anterior and posterior fins. From the formation of the pelvic plexus, some of the nerves going to which in FJasmobranchs are derived from vertebra', segments situated considerably in front of the fin, Davidoff * deduced the conclusion that the limbs had moved backwards from an orginally anterior position, and regards the facts which he adduces as favouring Gegenbaur's hypothesis. If, he supposes, the paired fins were derived from continuous lateral folds, they would be developed in the place they were ultimately to occupy, and there would be no trace of any previous shifting backwards or forwards. Gegenbaur f also has endeavoured to show that the discovery of the lateral ridges supports rather than overthrows his theory, — the ridges being persistent embryonic structures marking the passage backwards of the pelvic fins. Thacher (Proc. Connecticut Academy), J and, independently of him, Mivart (Trans. Zool. Soc. IX.) have sought to prove that a comparative study of the structure of the median and paired fins of adult Elasmobranchs and Ganoids leads to the same conclusion as the study of development, viz., that the paired and unpaired fins are strictly homologous structures, and are not developed by the modifiation of any pre-existing portion of the skeleton. In a subsecpient memoir § Balfour discusses the general bearings which he regards his embryological observations on Scyllium to possess upon the theory of the nature of limbs, pointing out that these observations are much more favourable to Thacher' s and Mivart's views than to those of Gesrenbaur and Davidoff. * Beitrage zur vergleichenden Anatomie der hinteren Gliediuasse der Fische, llorphol Jahrbuch, V., pp. 450-520 (1879.) t Zur Gliedniassen-Frage, Morph. Jahrb. V., pp. 521-526 (1879.) I I only know this memoir as quoted by Mivart, Balfour, and Davidoff. § On the Development of the Skeleton of the Paired Fins of Elasmobranchii considered in relation to its bearings on the Nature of the Limbs of the Vertebrata, P.Z.S., 1881, p.p. 656-670. 6 82 STUDIES ON THE ELASMOBRANCH SKELETON, " If Gegenbaur's view were correct we should expect to find in the embryo, if anywhere, traces of the second set of lateral rays ; but the fact is that, as may easily be seen by an inspection ot figures 6 and 7, such a second set of lateral rays could not possibly have existed in a type of fin like that found in the embryo. With this view of Gegenbaur's it appears to me that the theory held by this anatomist to the effect that the limbs are modified gill-arches also falls, in that his method of deriving the limbs from gill-arches ceases to be admissible, while it is not easy to see how a limb formed on the type of the embryonic limb of Elasmobranchs could be derived from a gill-arch wiih its branchial rays."* He also points out that Huxley's view that the proximal piece of the axial skeleton of the limb of Ceratodus is the mesopterygium, and that the fin of the Elasmobranchs is derivable from that of Ceratodus by the drawing in of the axis, is negatived by the proof afforded by the facts of embryology of the secondary character and late development of the inesopterygium. He shows also that the arrangement of the nerve-plexuses as described by Davidoff does uot necessarily require the explanation given by that anatomist. Tbe fact that some of the nerves which go to form the pelvic plexus are derived from vertebral segments in front of the position of the fins may be explained by a previously greater extent of the fin, just as well as by its movement backwards, f Finally Owen (Proc. Zool. Soc , 1883) has recently given a short summary of his views on the subject of the homologies of the vertebrate limb, and has shewn how his theory of the origin of limbs from lateral appendages of haemal arches gaius support from Balfour's investigations on the development of the fins of the Elasmobranchii. * I. c. p. 669. t I have ventured (On the Structure of the Paired Fins of Ceratodus. Proc. Linn. Soc, N.S.W., Vol. VII., p. 10.) to make the very obvious suggestion that the derivation of the pectoral and pelvic plexuses from a number of spinal nerves was a strong piece of evidence in favour of Balfour's theory and against that of Gregenbaur ; but I am now inclined to think, in view of certain facts observed by Furbringer (Morphologischea JahrbuBch, IX.) as to the origin of the nerves supplying the pelvic fin in some Teleostei with thoracic or jugular pelvis fins, that the position of the spinal nerves from which the plexuses are derived is too plastic a factor to support any wide generalisatioE at all. BY WILLIAM A. HASWELL, M.A., B.SC. 83 CARCHARODON RONDELETII. Plate I., Figs. 1-1. Skull and Visceral Arches. The upper surface_of the occipital region of the skull (Plate 1. fig. 1) is horizontally directed, and is continuous without in- terruption with the upper surface of the periotic and ethmoidal regions. The occipital crest is not well marked behind, but in front forms an elevated, though rounded, ridge, ending between the auditory foramina in a nearly vertical border. The parietal groove is shallow and open, and is excavated on the hinder part of a promi- nent parieto-frontal crest, which reaches as far forwards as the frontal foramen. A small median foramen lies in its front portion. On either side of the parietal groove, running forwards and slightly outwards, is a rounded elevation, which stops short a little way in front of the auditory foramen, and behind does not quite reach to the posterior margin of the skull. The anterior and posterior portions of this correspond to the elevations of the anterior and posterior semi-circular canals respectively. The vestibular promi nence is not well marked. The articular surface for the hyo-mandibular (Plate I., fig. 2, At.), is borne outwards and backwards from the cranium on a very prominent process, which is produced into thi-ee prominent angles, one directed backwards, a second upwards, backwards, and a little outwards, and a third, the shortest, forwards and outwards. The posterior portion of the process projects far behind the plane of the foramen magnum, and bears a large aperture for the glosso-pharyngeal on its upper and posterior surface at some distance from the posterior anglej but behind the plane of the foramen magnum and of the orifice of the vagus ; below it reaches to the plane of the base of the skull ; and the anterior and upper portion reaches as high as the middle of the foramen magnum. The articular surface itself consists of two portions — a hinder, much larger, which is a shallow concavity and is boundei below by a slight raised ridge ; 84 STUDIES ON THE ELASMOBKANCH SKELETON, and an anterior, smaller, saddle-shaped, and placed in front of and above the other, from which it is not distinctly separated. This large and prominent articular surface distinguishes the present genus very markedly, though modifications in the same direction are to be observed in the case of Galeus and Scymnus. There is no second foramen near that for the glossopharyngeal such as occurs in some genera. The orifice for the facial nerve is situated far forwards, separated by a considerable interval from the articular surface for the hyo-mandibular and near the trigeminal. The orbitis covered above by a wide lamellar roof produced behind into a post-orbital process ( Po 0) which is likewise lamelliform, and is curved downwards and backwards ; the latter does not come into direct relation with the palato-quadrate cartilage. In front, the roof bends down towards the base of the skull and bounds the orbit anteriorly, forming a distinct though not prominent prae- orbital process. Below, the orbit is bounded by a cartilaginous lamella which slopes downwards and outwards from the basis cranii. This lamelliform process or basal plate {Ba), is interrupted in front by a deep irregular incision, and behind there is a large oval foramen. On comparing the skull of Carcharodon with a dried skull of Lamna cornubica, I can find little difference between the two. In both are the same postero-lateral processes for the articulation of the hyo-mandibular ; in both the auditory foramina lie in a groove which runs along a broad central ridge ; in both thin lamellae of cartilage overarch the orbits ; and both have the same form of three-barred rostrum. As, however, the structure of the skull in the family to which both these genera belong has never been described, I have entered with some minuteness into the above description. The palato-quadrate is suspended, as in most Plagios tomes, by means of a hyo-mandibular, which is lai-ge and articulates with skull by a broad articular surface. Attached to the hyo-mandi- bular and hyoidean cartilages are about twenty irregular rays, with BY WILLIAM A. HASWELL, M.A., B.SC. 85 a number of smaller intercalary cartilages towards their extremities ; three of the rays on either side of the articulation between the hyo-mandibular and the hyoidean coalesce at their bases. The copulare of the first branchial arch articulates with the hyoid copula ; that of the second arch is united with its fellow by the intermediation Of a small copula ; it is connected externally with both the first and the second arches, as often occurs. The fifth arch has no copular. The basal plates of the first three arches are large and triangular ; the third is bilobed at the apex ; the mesial plates are deeply grooved internally near their proximal ends for the attachment of the strong adductors. The first arch has sixteen rays, the second thirteen ; the third twelve. The fourth basal is confluent with the upper mesial of the fifth, their being no representative of the fifth basal.* The mesials of the fourth arch are deeply grooved for the adductors like those of the preceding three which they resemble in form ; it has twelve rays. The fifth has no muscular grooves ; it has no rays, but presents a strong continuous ridge on its outer surface in a position corres- ponding with that of the rays in the preceding arches. The Shoulder-Girdle. The mesial portion projects very strongly ventrad, forming a fold, and its front margin is greatly elevated towards the middle. The lateral halves are united by continuous cartilage ; except at the dorsal extremities and the mesial uniting portion, they are strongly impregnated with osseous matter. The whole girdle is very broad, much broader than in Carcharias, slightly contracted near the line of junction, and narrowing slightly towards the dorsal extremity. There is no articular process or surface for the branchial skeleton. The articular surface for the pectoral fin is directed downwards and slightly backwards and outwards ; it is of long, narrow form, constricted in the centre. The arrangement of the nerve apertures is in some respects peculiar, and very different from that to be observed in Carcharias. \ The aperture of * A similar arrangement occurs in Raja, RUjiichobatus, Scyllium, and Galeus. Vide Gegenbaur, Untersuchungen, II., i., "Schultergurtel der VVirbelthiere." 86 STUDIES ON THE ELASMOBRANCH SKELETON, entrance is situated nearly directly behind the articular surface about the middle of the arch ; from this two canals lead, the one short and wide, passing outwards and a little forwards and downwards to open on the outer surface, the other narrow, and passing upwards, forwards, and slightly outwards to end above and behind the articular surface on the inner aspect of the cartilage close to the anterior border. The upper canal described by Gegenbaur in Scyllium, Oaleus and Pristiurus is indicated on the right side only by a slight depression. The Pectoral Fins. (Plate I., fig. 3.) As in Carcharias,* the pro- meso- and meta-pterygia are all well developed and the latter is greatly elongated, having a large number of rays articulating with its pre-axiad border ; but the mesopterygium is mt quite distinct from the metapterygiuui, in fact is completely coalescent with it at the base, whereas in Carcharias the two cartilages remain cpiite separate. Articulating with the distal extremity of the propterygium is a lateral cartilage, formed, as in Scyllium, Pristiurus and Carcharias by the coalescence of the bases of three posterior propterygial rays, but not continuous with the latter — being separated from them by an articulation or interval of fibrous tissue ; the front ray, which is very short, remains distinct and articulates separately with the propterygiuni. The propterygium and mesopterygium are relatively more important than in Carcharias, nine rays in all articulating with them ; the bases of the last four mesopterygial rays are coalescent for a short distance. The elongated metapterygiuui articulates at its distal extremity with two accessory cartilages, the posterior of which is much the longer and bears nine rays, while the anterior bears three. The bases of four of the rays which articulate with the metapterygium are coalescent in pairs for a short distance at the base. The arrangement of the basal cartilages described above seems to place the pectoral fin of Carcharodon in an intermediate position * Gegenbaur, " Untersuehunger zur vergleiehenUen Anatomie der Wirbelthiere." Heft, 2, 2te. Abschnitt, Brustflosse der Fische, p. 142, Tab. IX., fig. 5 (1365.) BY WILLIAM A. HASWELL, M.A., B.SC. 87 between that of Carcharias and that of Oallorhyaclms * — the basal elements in the latter being reduced to two, of which the posterior may be regarded as the homologue of a coalescent meso- and nietapter ygiu m . The whole of the long pointed fin of Carcharodon is supported by a framework of cartilaginous rays which extend nearly to its apex and are closely united into a continuous triangular plate. The middle rays, i.e., those which reach nearly or quite to the apex of the skeleton of the fin, broaden out considerably distally, and sometimes divide. Between the distal portion of adjacent rays in the front half of the apical part of the fin are intercalated a series of accessory rays, an arrangement which I have not met with in any other form, though a rudiment of it is traceable in Meter odontus Phillipi. The Pelvic Fins. The pelvic cartilage presents a large oval aperture in its outer half near the anterior border ; its outer extremity is produced into a process with which no fewer than six rays articulate. The basai cartilage is strong and curved, convex above, flat below ; at its distal extremity are two small cartilages with which the long tapering flexible cartilage of the clasper articulates. The last ray, which is very short, is attached exclusively to the base of the cartilage of the clasper. The Dorsal fins. (Plate I., fig. 4.) The dorsal fin is supported by a cartilaginous skeleton which is separated by a fibrous interval from the spinal column. It consists of about twenty-eight rays, which slope for the most part backwards and upwards. The first ray is very short, but presents traces of division into three segments. The second, which is a little longer, divides into two branches ; the third is simple, and consists of three segments, of which the basal is ranch the longest ; the fourth is bifurcated, and each of the branches presents two articulations. The next six rays are either distinctly bifurcated near * Vide Mivart, 1. c. 88 STUDIES ON THE ELASMOBRANCH SKELETON, the extremity or have intercalated rays between them ; none of the rest of the rays are distinctly branched. The last five or six rays, which are very short, are supported on a series of irregular basal cartilages. The arrangement of the articulations is such that there are three more or less complete antero-posterior horizontal lines of them ; that situated nearest the base is confined to the last eleven rays ; the middle one stretches completely across the fin from side to side and the distal one, situated not very far from the middle, extends in an irregular line from the seventh ray to the eighteenth. The second dorsal and anal fins are very small, and consist of a few irregular rays without basal plates, and separated by a well-marked interval from the vertebral column. The Caudal Fin. The caudal fin is supported both by supra-vertebral and by sub- vertebral cartilaginous rays, of which the latter are more highly developed than the former. The latter begin a little in front of the upward bend of the spinal column. The first is a short triangular piece articulating movably with two of the hypurals- The following five, which become successively longer, likewise articulate with the hypurals, but the remainder, which gradually decrease in size from before backwards, coalesce with the latter at their bases without the intervention of any articulation. The supi'a-vertebral rays begin a little behind the commencement of the sub-vertebral ; none of them coalesce with the neural arches. In front, where they are more irregular and more or less coalescent with one another, a few of them are separated from the neural arches by a slight interval occupied by fibrous tissue. In many cases a pair of rays may coalesce with one another ; otherwise they correspond in number with the vertebrse. HEPTANCHUS INDICUS. Plate I., Fig. 5. Skull and Visceral Arches. The occipital region is characterised by the presence of three ridges — a central one continuous with the spinous processes BY WILLIAM A. HASWELL. M.A., B.SC. 89 of the vertebrae, and two lateral ones continuous with the transverse processes. Its upper surface slopes obliquely upwards and forwards to the parietal groove, which is a deep pit continued forwards for a short distance by a rapidly shallowing concavity. The elevations for the anterior and posterior semi-circular canals are well marked and "prominent. The articular surface for the hyo-mandibular is simple and not raised from the general surface The orbit is bounded behind by a very prominent post-orbital process with which the palato-quadrate articulates. There is no basal plate ; in front of and below the orbit and projecting down- wards and outwards, is a prominent pointed process, the extremity of which is free ; this, according to Gegenbaur, corresponds to the ant-orbital cartilage in Rays ; it is not, however, related to the wall of the nasal capsule, but is placed behind the latter and arises from the contiguous portion of the base of the skull. The rostrum is represented by a pair of short processes of the ethmoidal region not extending beyond the level of the nasal cartilage. The walls of the nasal capsule are formed of cartilage only behind internally, and above, with a short external rim. The nasal cartilage is ring-shaped, with two short horas directed down- wards. Below the orbit there is, as in Hexanchus griseus and Heptanchus cinereus, an extensive vertical articular surface for the palato-quadrate. The hyo-mandibular is a long, narrow, curved and flattened cartilage bearing the hyoid at its distal extremity, and suspending also the palato-quadrate, though chiefly related to the hyoid. The hyoid cornua are very large : they bear a few delicate rays ; distally they articulate with the hyoid copula. The first branchial arch has no copulare ; its venti'al mesial cartilage is connected with the postero-external angles of the hyoid copula The following five arches have all well- developed copularia ; the second and third have distinct though small copulae ; the fourth has no separate copula, the latter having become fused with the left copulare. The fifth and sixth copularia unite with the basibranchial plate. The seventh arch has no copulare as well as no basal, its ventral is broad and flattened, and unites with the basibranchial plate. The 90 STUDIES ON THE ELASMOBRANCH SKELETON, basibranchial plate is broad and leaf-like in front, while behind it is produced into a rather slender process. This arrangement of the copulae differs from that observed in Heptanchus cinereus as described by Gegenbaur* in the absence of an independent copula for the fifth arch. In the first to the fifth branchial arches the basals of opposite sides touch one another in the middle dorsal line, the basals of the first being united with one another by- cartilage. The basals of the sixth do not reach to the middle line. There are small but distinct muscular grooves on the dorsal and ventral mesial cartilages. The external branchial arches are represented only by two pairs of cartilages in each ; the one is connected with the external end of the basal ; the other, which is much longer, with the ventral end of the ventral cartilage. The free ends of these two slender cartilages bend round the outer edge of the gill-partition towards one another, but do not meet. These obviously represent modified rays, and their presence would seem to indicate that the more highly developed external branchial arches of other Selachians are derived from greatly elongated rays which ultimately lose their connection with the internal arches. The Pectoral Fins. The pectoral fin is very similar to that of Hexanchus griseus as described and figured by Gegenbaur. The propterygium is small and beai-s no rays, articulating distally with the mesopterygium. The mesopterygium and the metapteiygium bear a nearly equal number of rays, a few of them being bifurcate. The metap- terygium beai-s a small articular cartilage at its extremity, and the latter sustains about four rays. The shoulder-girdle is remarkable for the presence in the middle ventral line of a distinct four-sided lozenge-shaped cartilage let in to the arch, as it were, in front. This is a condition which I have not observed or seen described in any other form : it does not seem to occur either in Heptanchus cinereus or * 1 c. p. 136, pi. XVIII., fig. 1. BY WILLIAM A. HASWELL, M.A., B.SC. 01 Hexanchus griseus.* The intercepted cartilage is temptingly like a presternal, but the absence of such an element in the skeleton of any group nearer than the Amphibia seems to preclude this explanation. The Pelvic Fins. (Plate L, fig. 3.) In the pelvic fin of Heptanchus indicus there are three distinct basal cartilages articulating with the pelvic girdle and bearing rays ; these represent the prse- meso- and meta-pterygia of the pectoral fin. The first (p. pt'.) is the ecpuvalent of the so-called pre-axial fin- ray. It is a small, pointed cartilage articulating with the antei'ior facet on the pelvic girdle, curving forwards and outwards and ending in a pointed extremity. By its outer posterior border it gives attachment to the four anterior fin-rays, of which the first two have their bases coalescent. The mesopterygium (vi.pt'.) is a small cmadrate cartilage articulating with the middle facet of the pelvic arch, and giving attachment to two fin rays f The remainder of the rays are attached along the outer border of the metapterygium (nit. pt'.) The latter is a long narrow cartilage, somewhat curved outwards. Distally it gives attachment to two cartilages ; of these that situated more dorsad is a small nodule, articulating with which is a long narrow ray-like cartilage ; the latter is applied closely to the dorsal surface of the cartilage of the clasper and strongly united with it by means of fibrous tissue ; the more ventrally placed of the two cartilages articulating with the extremity of the metapterygium continues the axis of the fin, gives attachment at the base of its outer border to the last of the fin-rays, and distally is succeeded by a smaller cartilage with which the principal cartilage of the clasper articulates. The axial cartilage of the clasper is a slender, slightly curbed cartilage, which presents no appearance of the longitudinal groove found in Crossorhinus. Distally it supports two small, blade-like freely movable ossified cartilages which are attached to its apex about the middle of their * Gegenbaur, Schultergnrtel der Wirbelthiere, Op. cit. Heft. 2. t If this middle basal cartilage is present in the European species it has escaped notice. (See Davidoff, Alorph , Jahrb. V. ; Mivart, l.c,p. 444, pi. LXXV., flg. 4.) 92 STUDIES ON THE ELASMOBRANCH SKELETON, length. The latter support the end of the groove of the clasper, and by their rotation can open or close it. The pelvic arch is narrow from side to side and very long antero-posteriorly — the greatest breadth being only about twice the length — convex ventrally, convave dorsally. Unpaired Fins. The dorsal fin is very simple, consisting of two broad and thin sheets of cartilage, an anterior and a posterior ; the former much the larger, having about 17 few-jointed rays united with their upper edge. Several of these rays are obscurely bifiurcate. This is very similar to the dorsal fin of H. chiereus* except that the posterior basal cartilage in the latter is very small. The anal fin is similar to the dorsal, but smaller and with fewer and shorter rays. CROSSORHINUS BARBATUS. Plate I., Figs. 6-8 and Plate II, Fig. 13. Skull and Visceral Arches. The cranium is very wide and depressed, as in Scyllitcm catidus, the interorbital breadth being relatively much greater than in Chiloscyllium. A noteworthy point in comparison with related genera is the much greater relative antero-posterior extent of the post-orbital region. The occipital surface slopes upwards and forwards, and meets the upper surface in a rounded ridge, in front of which the not very deep pai'ietal groove is situated. The upper surface of the skull in front of this is marked by a shallow mesial longitudinal depression, the continuation forwards of the parietal groove ; it is bounded externally by a continuous raised border as far as the pre-orbital process. The occipital region is not produced in the middle line behind. As in ScylUum, Mustelus, Galeus, and Scymnus, the lateral posterior *Mivart, 1. c, p. 443, pi. LXXV., fig. 2. BY WILLIAM A. HASWELL, M.A., B.SC. 93 processes which articulate with the first vertebra are prominent, the first vertebra being wedged very closely into the median recess between them and very closely united to the skull, except in the middle line above, where a considerable interval occupied by fibrous tissue intervenes between the hinder part of the skull and the neural arch.* The apertures for the vagi, which are very large, are placed immediately above and in front of these lateral processes, and above and a little external to them are a pair of smaller apertures of unknown function. There is no trace of a median occipital crest. In the auditory region the elevations corresponding to the anterior and posterior semi-circular canals are prominent, though rounded, and less sharply marked off than in some nearly-related forms ; between the anterior elevation and the lateral border of the skull is a rather deep hollow. The postero- lateral angles of the skull are somewhat curiously modified, the arrangement being more like that observed in Carcharodon than in Scyllium. The angles are drawn out into prominent processes, each of which exhibits three divisions, an antero-superior, an anteroinferior, and a posterior. The antero-superior is continued into the very prominent vertical ridge which separates off the upper surfaces of the cranium from the lateral. The antero- inferior forms the hinder portion of a ridge which bounds superiorly the articular surface for the hyo-mandibular. The posterior, which extends outwards and backwards, is grooved above for the glossopharyngeal, the aperture of exit of which is situated at its base ; below it developes a ridge with which some of the ligaments for suspending the lower jaw appear to have been connected ; this ridge occurs also in Cheiloscylliv.m ; it runs forwards and inwards and ends some distance behind the basal angle. The articular surface for the hyo-mandibular differs from that of all forms with which I am acquainted f in being a very deep, almost conical hollow, which is situated below and a little in front of the anteroinferior process already mentioned. It is in the * A similar arrangement occurs in Cheiloxcyllium. t The corresponding articular surface in Cheiloscyllium is a wide and shallow concavity without any definite upper border, but with the lower border rather prominent, and formtd by the ridge mentioned above as giving attachment to ligaments. 94 STUDIES ON THE ELASMOBRANCH SKELETON, same transverse plane as the point of junction of the anterior and posterior semi-circular canals, and therefore excavated in the side of the cranium proper and not on the postero-lateral process. The opening of the facial is directly in front of this articular cavity, and is separated by a broad ridge from that of the trigeminal. The supra-orbital ridge is very prominent and forms to some extent a roof to the inner part of the orbit ; it ends behind and in front in prominent post- and prae-orbital processes. There is a very broad and thin lamellar basal plate, nearly horizontal in position, but inclined slightly downwards externally ; it presents a rather small oval opening in its hinder portion close to the lateral wall of the cranium. The palato-basal articulation takes place through the interme- diation of a very thick and short ligament inserted immediately in front of the orbit, where there is a small but well-marked articular surface looking outwards and forwards. The ethmoidal canal is not even represented by a notch.* The prefrontal opening is large and its lateral borders diverge anteriorly unlike those of Scyllium. In front of it the basis cranii rises up and is extended into three thin lamellar processes, of which the middle one or rostrum is nearly straight and ends in a free extremity between the nasal capsules, while the lateral become rather expanded, and, their anterior ends curving downwards, form a part of the roof of the corresponding nasal capsule. Immediately behind the frontal foramen is a slender process which passing outwards and forwards, becomes greatly expanded at its extremity to form the outer and inferior wall of the nasal capsule. The labial cartilages form a chain of three strong bones on either side, forming a nearly complete ring round the mouth only inter- rupted by a space in the middle above and below. The proximal extremity of thehyomandibular presents anteriorly a stout peg-like process corresponding to the deep articular cavity of the side of the skull. Distally it presents a broad surface for the * This is a marked point of distinction between the present form and Scyllium and Clu i lose y Ilium. BY WILLIAM A. IIASWELL, M.A., B.SC. 95 palatoquadrate. The hyoid is a stout, gently curved, cartilage more than half as long again as the hyo-inaudibular. The rays are connected with the hyo-mandibular only near the skull, and with the hyoid for a short space some distance from the proximal end ; the two sets curve round and meet, leaving a wide opening opposite the articulation between the two cartilages ; they coalesce and sub- divide in a highly complex manner. The spiracular cartilage is a delicate lamella of oblong shape with the two inner angles and the antero-external produced into short processes. The body of the hyoid is rather narrower than the branchial copula and strongly arched forwards. Externally it presents two cornua an anterior short and stout for articulation with the hyoid and a posterior, rather longer for the copulare of the first branchial arch. The ventral mesials of the first four branchial arches are longer but narrower than the dorsals ; they both have deep excavations for the adductor muscles, those of the dorsal cartilages being the larger, and being perforated. The first arch bears ten rays, the second likewise ten, the third eight, the fourth six ; a number of the rays have hooked extremities. On the posterior border of each ventral mesial cartilage, in continuation of the row of rays, is a lamelliform process, very prominent in the first arch, becoming very low in the fourth. A. slender cartilage represents the dorsal end of an external branchial arch, and in the second, third, and fourth arches, but not in the first, an irregular flattened cartilage represents the ventral portion ; the first of these ventral cartilages of the external branchial arches is not connected with the internal arch ; the others articulate with the ventral mesials. The dorsal portion of the fifth arch coalesces as usual with that of the fourth. The dorsal mesial of the fifth is deeply excavated for the muscle ; the ventral slightly. The latter is much thicker than these of the preceding arches ; it presents two conical processes ; the one on its inner, the other on its outer surface, the latter nearly corresponding in position to the rays of the preceding arches. 96 STUDIES ON THE ELASMOBRANCH SKELETON, The first branchial arch has a short and thick copular which articulates with the hinder angles of the body of the hyoid. The copularia of the second arch are very long, and with those of the third articulate with the anterior border of a broad common copula. The latter, which is twice as broad as long, has a strongly convex anterior border, and a waved concave posterior border ; its outer border is directed slightly back as well as out, and with it the fifth arch articulates. It presents a trace on one side of a longi- tudinal division into three parts, the outer of which may represent the copular of the fifth. With the posterior border of the copula is articulated a short arrow-head-shaped urobranchial cartilage. Pectoral Fins. (Plate II., fig. 13.) The shoulder-girdle is characterised, in accordance with the general form of the animal, by its very great breadth — its transverse being much greater than its dorso -ventral extent — and also by the solidity of its texture — there being no mesial connecting portion of more flexible cartilage uniting the lateral halves as in other Shai-ks. The mesial or transverse portion of the arch is but slightly a ngulated ventrad in the middle. The articular surfaces are placed on prominent processes, the long axis of which is antero-posterior, or nearly so. In front of each of them, as in Cestvacion, is a very prominent crest, and between the articular surface and the crest is a very large foramen ; the second foramen is situated on the other side of the articular process, between it and the inner edge of the cartilage, at the ventral extremity of a wide shallow groove on the under surface of the lateral portion of the girdle ; a little on the ventral side of this opening is a conical tubercle. The lateral portions of the arch are strongly incurved, but their dorsal extremities are still widely separated from one another ; they end in a blunt point. In the skeleton of the fin itself the propterygium is well- developed, and consists of two nearly equal cartilages, the more distal of which has a narrow accessory cartilage running along its outer border. But the propterygium has no direct relation to any BY WILLIAM A. HASWELL, M.A., B.SC. 97 of the fin-i'ays. The mesopterygium consists of one elongated, slightly curved cartilage which bears on the distal half of its outer border a sei'ies of eight fin rays. The metapterygium is long and narrow, and bears eleven rays, a twelfth being borne ]>y the small accessory cartilage at the apex. The meso- and metapterygia are separated from one another throughout a considerable part of their length by a well-marked space. The rays are likewise separated at their bases by well-marked intervals ; distally, how- ever, they expand and become closely apposed, except in the case of about six of the inner rays, each of which becomes shortly bifurcated. The skeleton of the pectoral fin in the nearly related Ginglymostoma differs from that of Crossorhinus in the basal cartilages being relatively sirualler. In the existence of the interval between the mesopterygium and the metapterygium, the latter bears some resemblance to ChezloscyUium ocellatum, as described and figured by Mivart (1. o, p. 448, pi. LXXVL, fig. 4), but the space is very much larger in the latter. Pelvis and Pelvic Fin. (Plate I., fig. 8.) The pelvic cartilage is nearly straight, flattened from above downwards, and a little expanded at either end. The anterior basal cartilage is small and unimportant ; there is no mesoptery- gium, several rays articulating directly with the pelvis. The skeleton of the clasper consists of a long ossified cartilage marked on its dorsal aspect by a deep groove, the lips of which are closely approximated ; this axial cartilage ends distally in a strong pointed spine, articulated around the base of which and ensheathing it are four more or less scale-like pointed bones capable of being divaricated from the axis of the appendage so as to spread out in a l'adiating manner from the base of the spine. Unpaired Fins. The dorsal fins are of nearly equal size ; the anterior contains fourteen, the posterior fifteen rays, each, except the first two or three, with an expanded upper or distal piece, and each, with the 7 98 STUDIES ON THE ELASMOBRANCH SKELETON, exception of the last two or three, with a short basal element. In general structure these fins bears a close i-esemblance to the corresponding parts in (Jinglymostoma (Mivart, I.e., p. 446, pi. LXXVT., fig. 1), except that the rudimentary basal plate is not represented. The anal fin is smaller than the second dorsal, with fifteen rays of similar shape to those of the dorsals. There are fifty-five pairs of well-developed ribs. Of these a good many are divided into two segments. The caudal portion of the vertebral column is but slightly curved. Its neural rays, about forty-five in number, are nearly twice the length of the haemal rays. Of the peculiarities in the structure of the skeleton of Crosso- rliinus, the most noteworthy are the form of the articular cavity for the hyo-mandibular, the abnormal shape of the rostrum, the absence of the external branchial arches, and the rigid nature of the ventral portion of the pectoral arch. These, besides other less important characteristics, definitely mark off the genus from the Scyllidce with which it was previously placed. A characteristic feature of the skeleton of Crossorhinus is the presence throughout all the cartilages of innumerable small bony centres, giving the skeleton a remarkably hard and rigid texture. PRISTIOPHORUS CIRRATUS. Plate I., Pigs. 9-12. Skull and Visceral Arches. (Plate I., fig. 9.) In general form the skull, were the rostrum removed, would not be unlike that of Heterodontus. The plane of the occipital foramen is vertical. The surfaces of articulation for the hyo- mandibular are antero-posteriorly elongated and placed low down near the base, as in Rays. The auditory apertures are placed close together near the middle line, and are placed at the bottom of a deep excavation which is continued in front into a short shallow BY WILLIAM A. HASWELL, M.A., B.SC. 99 open groove. The post-orbital processes are not conspicuous. The palato-basal articulation is placed far back on a level with the hinder boundary of the orbit. The rostrum is formed of a mesial and two lateral parts ; the former being a prolongation of the roof and floor of the cranium, and containing a canal continuous with the cranial cavity and running forwards to the end of the snout. The lateral parts are continuous behind with the cartilage of the olfactory capsules ; they form thin plates bordering the mesial part and perforated by numerous apertures. The hyoid arch, as in Sharks generally, articulates above with the distal extremity of the hyo-mandibular ; ventrally it unites with a copula which has the form of a very narrow curved bar. Both the hyo-mandibular and the hyoid cartilages are provided with rays. The hyoid copula is represented by a transverse band. There is a common branchial copula without any trace of transverse division. The first branchial arch is connected not with this, but with the hyoid copula The second, third, and fourth arches have well-developed copularia, which decrease in size from before backwards. The muscular excavations on the first four arches are perforated by foramina. The external branchial arches are represented by slender cartilages. Pectoral and Pelvic Fins. (Plate I., figs. 11 and 12.) In the pectoral arch the hinge- like central portion found in other Sharks is not well marked, the two halves being capable of very little motion upon one another. As in the Sharks generally the dorsal ends of the arch are wide apart from one another and have no articulation with the spinal column. The propterygium is only represented by a slender, ray-like cartilage ; the mesopterygium and metapterygium on the other hand are well- developed, and contribute nearly equal shares to the support of the rays ; the metapterygium bears at its extremity a polygonal accessory cartilage with which a few short irregular i-ays articulate.* There is nothing in the * In the general arrangement of the cartilages there 19 a close resemblance to P.japonicus, as described and figured by Mivart (1. c, p. 453., pi. LXVIII., fig, 1.) 100 STUDIES ON THE ELASMOBRANCH SKELETON, structure of the pectoral fin presenting in any way an approxi- mation to the Rays. The pelvic arch is a nearly straight bar, slightly arched forwards in the middle, with short, broad, anteriorly directed processes at either end. There is a short pre-axial ray or propterygium, with which three short rays are connected ; there is no representative of a mesopterygium, but none of the rays articulate directly with the pelvic arch, the long narrow metapterygium supporting all the rest. Unpaired Fins. The unpaired fins present broad plate-like basal cartilages closely united with the vertebra?. The verteba? of Pristio2)horus present solid, deeply biconcave centi'a, which on a mesial transverse vertical section exhibit, as in the case of Selache, two pairs of cartilaginous tracts passing from near the cenfo-e to the supero-lateral and infero-lateral parts of the vetebrse. TRYGON PASTINACA. Plate II., Figs. 10-12. Vertebral Column. (Plate II., figs. 10 and 11.) The anterior vertebral plate presents a very prominent, con- tinuous, spinous ridge. In the hinder half of the plate the transverse processes are likewise developed on each side into a wide thin lamina perforated at its base by 9 or 10 irregular apertures. In front this lamina is developed into a free flap. Behind it is continuous with a plate of cartilage which stretches horizontally across the middle line, becoming synchondrosed with the spinous ridge. The horizontal plate corresponds to the horizontal bar found in a corresponding position in Hypnos, but, differs from the latter in being closely united with the spinous ridge. It is connected externally, as in Hypnos also, with the pectoral arch, the connection being effected by means BY WILLIAM A. HASWELL, M.A., B.SC. 101 of a somewhat complicated articulation. Each lateral lamella, formed apparently as above noted by the transverse processes, developes just below the part where the mesial bar arises from it, a thick, laterally projecting process with a truncate terminal face ; above and a little behind this is a wide aperture in the root of the horizontal lamella into which the dorsal end of the pectoral arch fits, while the truncate lateral process articulates with a concave oval surface on the inner border of the arch at some little distance below. There is a considerable resemblance between this arrangement and that already described as occuring in Trygonorhina, except that in the latter there is no connection between the horizontal bar and the lateral laminae, and the articulation with the pectoral arch is effected entirely through the former, which is a development from the spinous ridge. Another peculiarity which the anterior vertebral plate of Trygon presents is the presence of a series of articular facets for the branchial arches. The chief of these articular surfaces is that for the fifth branchial arch ; this is situated on a little angular projection on the lateral border of the vertebral plate, close to the front portion of the lateral lamina. In front of and a little internal to this on the ventral surface of the plate is a pair of short triangular ridges ; these articulate or are synchondrosecl with the basal plates of the fourth branchial arch. In front of and a little external to those, near the lateral borders of the plate, is a pair of small elevations which articulate with the third branchial arch. There are no ribs attached to any part of the spinal column. Skull and Visceral Arches. (Plate II., fig. 12.) In the skull the plane of the foramen magnum is very nearly vertical. The occipital condyles lie a little behind, on projecting processes. The orifice for the vagus is close to the foramen magnum. The elevations for the anterior and posterior semi circular canals are tolei'ably well marked. The orifices of the auditory organs are situated far apart, and are not connected by 102 STUDIES ON THE ELASMOBRANCH SKELETON, any common groove or depression. The articular surface for the hyoid is an antero-posteriorly elongated surface placed close to the base of the skull. In front of it is a wide bridge of cartilage for the protection of the facial. Behind it are the two small articular facets with which the hyoid and first branchial arches articulate. These are borne on a rather conspicuous ridge, which in front forms the posterior and upper boundary of the articular surface for the hyo-mandibular, and behind is continuous with the processes bearing the occipital condyles. The post-orbital process takes the form of a long and broad, thin lamina of cartilage stretching outwards and forwards from the post-orbital region of the roof of the skull. The cavity of the cranium dilates con- siderably in front towards the region of the olfactory capsules, which are greatly elongated transversely and connected together in the middle line. The prse-frontal foramen is very wide, and is continuous behind with the supra-cranial fontanelle. The praeorbital process has the form of a short pointed projection- The ant-orbital cartilages are vertically compressed, blade-like laminae articulating with the lateral angles of the olfactory capsules and directed backwards and outwards. The hyo-mandibular is made up, as in most Rays, of two distinct segments, of which the distal is much the smaller. In Trygon, as in many of the Batoidei, the ventral elements of the hyoidean arch are not connected with the hyomandibular. In Trygon pastinaca they articulate directly with the periotic region of the skull just behind the surface of articulation for the hyo-mandibular. The hyoid is intimately connected with the first branchial arch, and the latter in turn also articulates with the auditory region of the skull behind the articulation for the former. The hyoid arch, as in Rays generally, has but a slender copula, and articulating with the ventral extremity of each ventral mesial is a flattened bar of cartilage, which passes almost straight forwards to end in a free extremity ; this seems to represent the copulare. by william a. haswell, m.a., b.sc. 103 Pectoral Fins. The pectoral arch is characterised by the solidity of its structure and the massiveness of its lateral portions. The upper and lower nerve-foramina are very large ; thei'e are no accessory foramina as in Trygonorhina. ThB articular surfaces for the fin are placed on a horizontal ridge, at the extreme anterior and posterior ends of which are placed the surfaces for the propterygium and the metap- terygium respectively ; the former is a long oval with the long axis vertical and the surface directed outwards ; in the intermediate ridge is a concavity for the mesopterygium. Close to the inner lateral border of the arch is the articular surface for the fifth branchial arch, which is double and somewhat raised above the general surface. The propterygium has articulating with its distal extremity a stout ray with which are connected a number of fin rays. The mesopterygium is very small but occupies all the interval between the propterygium and the meta pterygium; none of the rays articulate directly with the shoulder girdle. The ru eta pterygium is divided into four segments. The pelvic arch is a strongly curved cartilage which is produced behind over the acetabular facet into a strong spine ; a little in front of this it develops a prominent angular ridge on its outer surface. The metapterygiurn bears distally two very short cartilages which continue the axis of the fin and give origin to a few short rays ; the mesopterygium is not represented. UROLOPHUS, sp. 1 Plate II., Fig. 14. The main difference between the skeleton of this species and that of Trygon pastinaca consists in the presence between the nasal cartilages of a pair of very slender, crescentic, cartilaginous cornua, attached to, but not continuous with, the cartilage of the front of 104 STUDIES ON THE ELASMOBRANCH SKELETON", the skull. These are inclined downwards and backwards and may represent upper labial cartilages, or may perhaps be regarded as representing a rudimentary rostrum. The anterior vertebral plate presents laterally very broad and long wings representing the coalescent and produced transverse processes. In the middle it presents a prominent vertical lamina formed of the coalescent spinous processes. This ends some distance in front of the position of the shoulder girdle, with which it has no connection. There are thirty pairs of ribs, of which the majority are of considerable length. HYPNOS SUBNIGER. Plate XL, Figs. 6-9. Skull and Visceral Arches. (Plate XL, figs. 6 and 7.) In general shape the skull recalls to some extent that of Heterodontus. It is long, rather narrow and high, broadest behind in the occipital and auditory regions, narrower between the orbits and becoming broader again in front in the olfactory region. The foramen magnum is very large ; its plane is very oblique, and a large space occupied only by membrane intervenes between the upper border of the foramen and the commencement of the neural arches of the vertebra?. The condyles, as in Torpedo, are placed close to the foramen magnum. As in Torpedo, also, the aperture for the vagus is very large. Immediately above and a little in front of it is a short but well-marked process directed outwards ; this is rudimentary in Torpedo. Below and behind the foramen the postero-external angle of the skull is drawn out into a dorso-ventrally compressed process with the extremity of which the basal cartilage of the first branchial arch articulates. This is an arrangement which seems, so far as I have observed, to be peculiar to this genus. As in Torpedo, the articular surface for the hyo. mandibular is long, narrow, and nearly horizontal, situated low down nearly on a level with the base of the skull. The elevation BY WILLIAM A. HASWELL, M.A., I3.SC. 105 marking the position of the posterior semi-circular canal, which is absent in Torpedo, is well-developed in the Australian genus. Neither the prse-orbital nor the post-orbital processes are developed, and the orbit is devoid of basal plate. There is neither ethmoidal notch nor foramen. The olfactory region resembles that of Torpedo but there are no distinct praeorbital processes, and the fins articulate with the anterior extremities of the nasal capsules. The hyo-mandibular is a long cartilage, longer than the greatest width of the skull, dorso-ventrally compressed and broad proximally, but narrowing distally ; it is divided into two by a distinct transverse suture (as in many Kays) the outer piece being much shorter than the inner. Both upper and lower jaws are extremely slender. The hyoid arch is small, and quite similar to, though smaller than the branchial arches ; above it is incomplete, and not in any way connected either with the skull or with the hyo- mandibular, its dorsal end articulating with the basal of the first branchial arch, which articulates with the postero-external process of the skull in the manner already noticed. Though this arrange, ment of the anterior visceral arches is not, as will subsequently be seen, peculiar to the present form, it is a moditication which has hitherto escaped notice. In the Sharks the hyoid arch proper (which is much more important and much more sharply marked off from the branchial arches than in the Rays) is suspended from the skull by means of the hyo-mandibular, with which it articulates towards its distal extremity. The hyo-mandibular cartilage is thus in the Selachoidei a true hyo-mandibular suspensorium. But in the majority of the Rays, as pointed out by Gegenbaur, it has no such dual function, the hyoid arch being but slightly, if at all, connected with it, and its sole function being that of a mandibular suspensorium. In Torpedo the basal of the hyoid arch unites with the postero-lateral angle of the skull ; it is free below except where a short cross-piece unites it with the ventral end of the first branchial arch. The first branchial arch is attached to the ventral end of the second, and the second and third have each distinct copular pieces uniting with the basilar plate. 106 STUDIES ON THE ELASMOBRANCH SKELETON, The arrangement of the rest of the branchial apparatus in Hypnos is likewise peculiar. The copular elements of the hyoid and of the first, second, and third branchial arches are united below on either side to a thick longitudinal bar of cartilage which unites behind to the basi-branchial plate, close to its fellow, but diverges in front so as to leave a considerable triangular space, and ends in a free thickened extremity some little distance in front of the hyoid arch. Though these bars present no trace of longitudinal division they seem to correspond to the copularia of the hyoidean and three anterior branchial arches. The fourth and fifth branchial arches unite dorsally, as very commonly occurs, the basal of the fifth arch not being represented ; from their point of union a long process passes inwards and backwards. The fifth arch has an articulation with the shoulder girdle. Pectoral Fins. (Plate II., fig. 8.) The shoulder-girdle is distinguished by the slenderness of its mesial ventral portion, which, as in Rays generally, is formed of one continuous bar, not interrupted by any fibrous interval such as occurs in Torpedo. It bears externally the lateral masses of cartilage with which the pectoral fins articulate, and an upwardly directed process of each lateral mass is movably articulated with a dorsal bar of cai-tilage which runs inwards towards the middle line of the dorsal surface. The dorsal ends of these two bars are united by a flattened mesial cross-piece, which is placed well above the vertebral column, not being connected with it save by fibrous tissue. Such an entire absence of cartilaginous connection between the pectoral arch and the spinal column is found in no other Eay with the exception of Torpedo. (Vide Gegen. Unters. II., 1, p. 81.) The three facets for the pectoral fin are borne on three short processes. The propterygium is made up of no less than nine joints which decrease in size distally, the whole having much the appearance of a magnified fin-ray. The mesopterygium is a small cartilage shorter than the propterygium, and is divided into seven segments. Each of the rays of the fin is bifurcate at the tip. BY WILLIAM A. HASWELL, M.A., B.SC. 107 The cephalic fin consists of two curved cartilaginous styles connected with the skull as above noticed, having a series of short irregular rays attached along their anterior border, and of a series of irregular rays between them. The latter are not directly connected with the skull, and do not form a rostral prolongation of it as in Torpedo . Pelvic Fins. (Plate II., fig. 9.) The pelvic arch is a straight, rather narrow bar, continued externally into a pair of long, pointed, lateral processes directed forwards and outwards. The axial cartilage of the fin is narrow and pointed. Nearly all the fin-rays are bifurcate. The anterior rays articulate directly with the pelvic girdle, the first being shorter than the rest and repi'esenting the pre-axial fin-ray ; there is no basal cartilage representing the mesopterygium. There are two distinct dorsal fins of about ten to twelve rays each, placed close to one another on the short tail. The caudal fin itself is very small. TRYGONORHINA FASCIATA. Plate II., Figs. 1-5. Vertebral Column. The antei^ior vertebral plate presents a very strong odontoid process with a crescent-shaped articular surface at its extremity, and at the base of the odontoid process two concave articular surfaces for the occipital condyles. The spinous processes of the anterior vertebral plate are combined into a very prominent mesial ridge, and the transverse processes are likewise amalgamated, as in Rays generally, and develope about the middle of the length of the plate on either side a strong vertical process which reaches nearly as high as the spinous ridge. The spinous ridge ends some distance in front of the hinder extremity of the vertebral plate, and behind it 108 STUDIES ON THE ELASMOBRANCH SKELETON, is a much smaller lamella which develops lateral projections embracing the dorsal extremities of the pectoral arch, so as to form sockets for the reception of the latter. There are about twenty-five pairs of rather long slender ribs. Skull and Visceral Arches. (Plate II., figs. 1 and 2.) In general form the skull is somewhat expanded laterally and depressed dorso-ventrally, distinguished by its elongate rostrum and large olfactory capsules. The plane of the foramen magnum slopes slightly forwards. Below it is the deep mesial excavation for the reception of the odontoid process, the concave articular surface for which is nearly as wide as the foramen. The condyles are borne on short lateral processes. The vagus foramen is separated by a considerable interval from the foramen magnum. Immediately in front of and external to it is a slender bridge of cartilage. The articular surface for the hyo-mandibular is long and narrow, placed, as in Hypnos, close to the base of the skull and extending on to the postero-lateral process. The auditory foramina are very large, and are placed well apart from one another, only a very slight depression connecting them.* The elevations marking the position of the anterior and posterior semi-circular canals are very well-marked. Behind the orbit is a distinct post-orbital process, and in front of it are the very large and laterally pi'ojecting olfactory capsules. As in the Batoidei generally theie is no basal plate. The foramen for the trigeminal is separated from that for the facial by a slight interval ; behind the latter as in Rhynchobatus is an oblicpiely-placed bridge of cartilage. With the outer and posterior angle of the olfactoiy capsules is connected a compressed, curved, pointed cartilage, which represents the lateral process of the ethmoidal region of Rhynchobatus. * The absence of a deep parietal groove seems to he characteristic of the Batoidei. BY WILLIAM A. HASWELL, M.A., B.SC. 109 The rostrum is a long spoutdike structure, the concavity in which is continuous behind with the cerebral cavity. In front it gradually narrows, the excavation becoming shallower, and expands at the extremity into a thin sheet with a truncated terminal border ; near each angle of the flattened terminal portion of the rostrum is a small rounded aperture. The hyo-mandibular begins above in a broad extremity which articulates with the surface already noticed on the auditory region of the skull. Dorsally it presents a prominent ridge. The hyoidean arch is incomplete dorsally and becomes articulated to the dorsal mesial of the first bi'anchial arch. The latter developes a short pi'ocess which, as in Hypnos, articulates with the occipital region of the skull behind the surface of articulation for the hyo-mandibular. The copulare of the hyoid is produced anteriorly into a prominent flattened process. The hyoid copula is represented by a very long, slender, ribdike cartilage, which is not expanded into any broad mesial plate. The basal of the first branchial arch is in very close relationship to the ventral surface of the spinal column. The mesials of this and the three following arches present very deep and wide muscular fossa? which pass into one another across the articulation. The ventral mesial cartilage of the first branchial arch developes a flattened anterior process which articulates with the hyoid capula ; behind it articulates with the second branchial arch at the point of junction of the ventral mesial and the copulare. The second arch has a strongly curved ribbondike copulare ; those of the third and fourth are united ; the fifth arch has no copulare. The copularia of the second, third, and fourth arches, and the ventral mesial of the fifth articulate with a very wide basi-branchial plate. The ventral mesial of the fifth articulates with the shoulder girdle. Pectoral Arch and Pectoral Fins. (Plate II., figs. 3 and 4.) The pectoral arch is remarkable on account of the size and form of its lateral masses. The whole girdle has the form of an oval hoop, with the long axis transverse, the ventral side straight and the lateral portions greatly expanded. There is a narrow dorsal 110 STUDIES ON THE ELASMOBRANCH SKELETON, interspace, the pointed dorsal extremity of each half of the arch being received into a socket formed for it by a produced portion of the spinous ridge of the anterior vertebral plate in such a way that motion is only possible round a transverse axis passing through the two joints. The outer border of the transversely expanded lateral portion of the girdle gives origin behind nearly at right angles to an exti*emely prominent lamella, concave inwards and convex out- wards and directed outwards as well as backwards. This lamella pre- sents externally four horizontal ridges, the most prominent being the third reckoning from above downwards. This ridge connects the articular surfaces for the pro- meso- and metapterygia, and between the two last itself gives attachment directly to a number of fin-rays. The articular surface for the propterygium is placed on the produced border by which the expanded part of the hoop and the lateral lamellae unite. A little behind it is the less prominent articular surface for the mesopterygium. Between the two are two large nerve foramina, the one above and the other below ; these pass directly from within outwards. The articular surface for the metapterygium is placed on the posterior border of the lateral plate at the extremity of the prominent ridge ; it is a little less conspi- cuous than that for the propterygium. About midway between the ridge which bears the articular surfaces and the one above it is a horizontal row of fine small pores. The articular surface for the branchial arch is an ovate elevation situate close to the inner border of the lateral portion of the arch. The ventral bar is deeply grooved below. Among described forms the shoulder-girdle of Trygonorhina approximates most nearly to that of Rhino- batus (Gegenbaur, 1. c. II., p. 82, pi. V., fig. LA.) The propterygium consists of a stout proximal portion with four short distal joints, with the extremity of the last of which three irregular rays articulate. The mesopterygium is small ; between it and the metapterygium is a wide interval where the fin rays articulate directly with the shoulder-girdle itself. The metapteiy- gium is smaller than the propterygium ; two short cartilages are added to its extremity. The majority of the fin-rays of the pectoral fin bifurcate at their extremity. BY WILLIAM A. HASWELL, M.A., B.SC. HI Pelvic Fins. (Plate II., fig. 5.) The pelvic arch is very slender and very wide from side to side, as in Rays generally. Its lateral extremity presents two articular surfaces, one for the propterygium (pre-axial fin-ray) the other for the metapterygium. The mesopterygium is not represented. In front of the articulation a strong compressed process extends forwards and outwards, and behind on the dorsal surface just over the two articulations is a very prominent, slender, curved process which extends backwards and upwards. The propterygium con- sists of a long and three short joints, the last bearing several rudimentary fin rays. The metapterygium consists of a long basal joint and three shorter distal segments ; it bears twenty-four rays none of which are bifurcated. Unpaired Fins. The dorsal fin is small, with about fourteen rudimentary rays supported on two elongated, laterally compressed cartilages, the continuity of which with the spinous processes is manifest. The anal is very similar to the dorsal. The caudal is rudimentary. The dorsal fin is described and figured by Mivart, 1. c, p. 454, pi. LXXV1IL, fig. 6. SUMMARY. In the following summary are enumerated the principal characteristics of the skeleton in such families of the Plagiostomi as I have had the opportunity of examining. The division of the Selachoidei into two principal sub-orders — the Palceoselachii and the Neoselachii — seems to me to follow as a necessary conclusion from the researches of Gegenbaur on the anatomy of the skull. The prefixes have reference, I need hardly add, not to the relative geological age of the two groups, but to their relative degree of specialisation ; the structure of Notidanvs is certainly much more archaic than that of any other Shark. 112 STUDIES ON THE ELASMOBRANCH SKELETON, SELACHOIDEI. In the skull the post-orbital processes are usually well developed, the orbit is usually provided with a cartilaginous floor formed of the basal plate ; there is always a palato-basal articulation ; the rostrum usually consists of three bars with large foramina at the base. There are a series of external branchial arches ; the first branchial arch never articulates with the skull ; the hyoid arch is supported by the hyo-mandibular ; the copula of the hyoid has the form of a broad plate connected with its distal extremity. The pectoral fin is not connected with the skull by means of an ant- orbital cartilage ; the ventral portion of the pectoral arch is divided in the middle by a more flexible portion into two lateral halves usually slightly movable on each other, and the dorsal extremities do not articulate with the spinal column. The pro- and meta-pteiygia of the pectoral fin are never greatly elongated and usually have the form of relatively broad plates. PALuEOSELACHII. (NOTIDANIDiE.) The vertebral column is scarcely ossified. There are two neural arches for each centrum, at least in the caudal region. The occipital region of the skull is not so sharply marked off from the spinal column as in other Elasmobranchii ; it presents above a mesial ridge continuous with the spinous processes, and at the sides riclges continuous with the line of the transverse processes. The plane of the occipital region is vertical or inclined from below upwards and backwards. There is no lateral occipito- vertebral articulation. The principal vagus foramen is placed far from the foramen magnum ; the lower roots of the nerve pass out by from three to five distinct canals which are in line with the foramina for the spinal nerves. The vestibulum forms a distinct eminence on the surface of the infero-lateral portion of the auditory region. The articular surface for the hyo-mandibular is simple and not sharply marked off from surrounding parts. The post-oi"bital process presents an articular surlace for the palato- quadrate. The orbit has no cartilaginous floor. There is an BY WILLIAM A. HASWELL, M.A., B.SC. 113 ethmoidal canal. There is no tri-radiate rostrum. Representing the ant-orbital cartilage of Rays is an ant-orbital process. There are either six or seven branchial arches ; the external arches are incomplete. There is only one dorsal fin ; its rays are supported by a broad basal cartilage. NE0SELACH1I. The centra of the vertebrae are well ossified. The occipital region is well marked off from the vertebral column. The plane of the foramen magnum is vertical or slopes forwards. The principal vagus foramen is usually approximated to the foramen magnum, and there is never a row of accessory foramina in line with the foramina for the spinal nerves. There is no distinct elevation on the surface of the skull marking the position of the vestibule. The articular surface for the hyo- mandibular is complex. The post-orbital process never presents an articular surface for the palato-quadrate. The orbit has a cartilaginous floor. There is no process representing the ant- orbital cartilage of the Rays. There are never more than five branchial arches. There are two dorsal fins which may or may not present broad basal cartilages. Cestraciontid^e. The centra of the vertebra? present radiating bony lamellae. There is only a small tubercle representing the occipital crest, and the occipital region is sharply marked off from the vertebral column. The principal vagus opening is placed close to the lateral occipital process, and there is no row of accessory foramina. The elevation marking the position of the posterior semi-circular canal is placed on the posterior aspect of the cranium ; there is no distinct elevation for the vestibule. There is an ethmoidal canal. The auditory foramina open at the bottom of a fossa which is continued forwards into a groove excavated on a longitudinal mesial ridge. The orbit has a cartilaginous roof. There is no prominent rostrum ; the ethmoidal region is longer than in other 8 114 STUDIES ON THE ELASMOBRANCH SKELETON, Selachoidei, and the olfactory capsules are remote from the orbits. The hyo-mandibular takes a comparatively unimportant part in the suspension of the lower jaw and palato-quadrate. There are two dorsal fins, and these possess broad plate-like cartilages, and are closely related to the spinal column. LAMNID.E. The centra of the vertebrae present radiating lamellae. The articular surface for the hyo-mandibular is simple, but borne on a projecting portion of the postero lateral region of the skull. The post-orbital process does not articulate with the palato-quadrate. The orbit has a cartilaginous floor. There is no ant-orbital process representing the ant-orbital cartilage of the Rays. The external branchial arches are well-developed. There is a well developed three-rayed rostrum. The hyo-mandibular bears a series of cartilaginous rays. The hyoid copula is a broad plate. The meso- and metapterygia are partly coalescent ; the primary rays of the pectoral fins have intercalated among them a series of accessory rays which do not reach the basal cartilages. The dorsal and anal fins possess no broad basal cartilages and do wot articulate with the spinal column. ScylliolamnidjE. The centra of the vertebrae present radiating lainellse. The articular surface for the hyo-mandibular is a deep conical hollow into which fits a peg-like process of the latter cartilage. The rostrum is single, and does not advance much beyond the level of the olfactory capsules. There is a basal plate forming a floor for the orbit. There is neither ethmoidal canal nor notch. There are rays on the hyo-mandibular as well as on the hyoid arch. The hyoid copula is a broad plate. The external branchial arches are rudimentary. The pectoral arch presents no ventral mesial flexible interval as in other Sharks. All the three basal cartilages of the pectoral fin are well-developed. The unpaired fins do not present expanded basal plates. BY WILLIAM A. HASWELL, M.A., B.SC. 115 SCYLLID.E. The centra of the vertebrae present radiating lamellae. The articular surface for the hyo-mandibular is situated in great part on a postero-lateral process of the skull ; it is saddle-shaped, and not very deep. There is no ethmoidal canal. The rostrum is three-barred. The dorsal fin has no broad basal cartilages. Rhinidjb. The centra of the vertebra? are devoid of radiating lamellae. The post-orbital process is produced forwards and unites with the praeorbital process. The shoulder-girdle i-eseinbles that of the Rays in presenting a rigid ventral portion ; and the skeleton of the pectoral fin has the pro and meta-pterygia elongated in an antero-posterior direction as in the Rays. The skeleton of the dorsal fin presents wide basal cartilages apparently continuous with the neural spines, and has no distinct rays. PRISTIOPHORIDiE. The centra of the vertebrae are devoid of radiating lamellae of bone. The ethmoidal region of the skull is produced forwards into a long, dorso-ventrally compressed rostrum, perforated by a longi- tudinal canal, which is continuous behind with the cranial cavity. The copula of the hyoid is reduced to the form of a narrow strip of cartilage. There are rays on the hyo-mandibular as well as on the hyoid arch. The propterygum is very small. The dorsal fins are supported by broad thin plates continuous with the neural arches of the vertebrae. BATOIDEI. The post-orbital processes are small or absent ; the orbit is devoid of cartilaginous floor. There is no palato-basal articulation. The rostrum, when present, is usually imperforate at the base. There are no external branchial arches ; the first branchial arch is sometimes directly connected with the skull. When the hyoid arch is supported by the hyo-mandibular the articulation takes 116 STUDIES ON THE ELASMOBRANCH SKELETON, place near the proximal extremity of the latter. The ventral portion of the pectoral arch forms a continuous and rigid bar ; the dorsal extremities of the arch are connected either with the spinal column or with one another. The pro- and metapterygia of the pectoral fins have the form of elongated narrow bars, and the mesopterygium is insignificant. The anterior portion of the pectoral fin is connected by a cartilage — the antorbital cartilage — with the ethmoidal region of the skull. Pristid^e. The ethmoidal region of theskull is prolonged forwards into a very long, straight, dorso-ventrally compressed rostrum, traversed by a median and two pairs of lateral longitudinal canals. The first dorsal fin has broad basal cartilages apparently continuous with the neural spines, and a series of short rays. Khinobatid^e. The ethmoidal region of the skull is produced into a rather long rostruru. The first branchial arch articulates with the skull. The hyoid arch is not connected with the hyo-mandibular. The copulari of the branchial arches are distinct from the copula?. The dorsal fin has broad basal cartilages, apparently continuous with the neural spines, and a series of short rays. The pectoral arch articulates directly with the spinal column. The pro- and metapterygia are segmented ; between the mesopterygium and the metapterygium a number of the rays articulate directly with the shoulder-girdle. There ai'e well-developed ribs. TORPEDINIDiE. The ethmoidal region is not produced into a rostrum. The articular surface for the hyo-mandibular is not wide. The copularia of the branchial arches are distinct from the copula?. The hyoid arch is not connected with the hyo-mandibular. The pectoral arch is not directly connected with the spine ; it is not so rigid in the middle ventral line as that of other Batoidei. The anterior portions of the pectoral fins are detached, and articulate with the front of the ethmoidal region of the skull. None of the rays articulate directly with the shoulder-girdle. There are well developed ribs. by william a. haswell, m.a,, b sc. 117 Rajid^:. The articular surface for the hyo-niandibular is borne on a prominent process of the postero-lateral region of the skull. The ethmoidal region is produced into an undivided rostrum. The hyoid arch is connected with the base of the hyo-mandibular. There is only one branchial copula ; the copularia are not amal- gamated with it it, The pectoral arch articulates directly with the spinal column. The propterygvu/m articulates with the skull by means of an ant-orbital cartilage ; the pectoral fin is interrupted in front, with no detached cephalic fin. Short ribs are present. Some of the rays of the pectoral fin articulate with the shoulder- girdle. TRYGONIDiE. There is no distinct rostral prolongation of the skull. The articular surface for the hyo-mandibular is elongated antero-pos- terioi'ly ; it is situated near the base of the skull, and not borne on a prominent process. The branchial copula is coalescent with the copularia. The hyoid arch sometimes articulates with the proximal extremity of the hyo-mandibular, sometimes with the cranium directly. The pectoral fins are continuous in front ; the pectoral arch articulates with the spinal column. None of the rays of the pectoral fin articulate directly with the pectoral girdle. There are no ribs. Myliobatil\e. The cranium is elevated in front. There is no distinct rostrum. The articular surface for the hyo-mandibular is a tolerably deep hollow, situated close to the base of the skull, but not so much elongated as in most other Rays. The branchial copularia coalesce with the copulae. The hyoid arch is not related to the hyo- mandibular nor to the skull, but articulates with the base of the first branchial arch, which articulates with the skull behind the hyo-mandibular. The pectoral fins unite in front of the skull ; the pectoral arch articulates with the spinal column. There are no ribs. 118 STUDIES ON THE ELASM03RANCH SKELETON, Explanation of the Plates. Au — Auditory apertures in parietal groove. Ar — Articular surface for hyo-mandibular. PSC — posterior semi-circular canal. ASC— anterior seini-circular canal. Po 0 — post-orbital process. Pr 0— prse-orbital process, fo — fontanelle. or— foramen of exit of ophthalmic nerve from the orbit— op1 foramen by which the ophthalmic nerve passes downwards and outwards towards the nasal capsule (posterior opening of the ethmoidal canal ) R — rostrum. 01 — Olfactory capsule. Vg — foramen of exit of the vagus nerve. II— foramen for the optic nerve. Bp — Basal plate. PI-- palato-quadrate. Mck — -Meckel's cartilage. HM — hyo-mandibular. Hy — hyoid arch. Br1, Br2, etc. — Branchial arches, p pt — propterygium. m pt — mesopterygium. mt pt — metapterygium. p — pectoral arch, pi— pelvic arch, ppt' — anterior basal cartilage of pelvic fin. m pt' —middle basal carti- lage of pelvic fin. mt pt' posterior basal cartilage of pelvic fin. cl. — axial cartilage of clasper. Plate I. Fig. 1. Skull of Carcharodon Rondeletii from above. „ 2. The same from the side. ,, 3. Pectoral fin of the same. ,, 4. Dorsal fin of the same. ,, 5. Pelvic fin of Heptanchus indicus. M pt! — mesial basal cartilage . ,, 6. Skull of Crossorhhius barbatus from above. ,. 7. Pectoral fin of the same. ,, 8. Pelvic fin of the same. ,, 9. Skull of Pristiophorus cirratus from above. „ 10. Branchial skeleton of the same. „ 11. Pectoral arch and pectoral fins of the same. ,, 12. Pelvic arch and pelvic fins of the same. Plate II. Fig. 1. Skull of Trygonorhina faseiata from above. ,, 2. Branchial skeleton of the same. j, 3. Lateral view of pectoral arch of the same. Sf — superior nerve- foramina, if, inferior nerve foramina, p, facet for propterygium. m, facet for mesopterygium. mt, facet for metapterygium. ,, 4. Pectoral fin of the same— r — rays articulating directly with the pectoral arch. ,, 5. Pelvic arch and pelvic fins of the same. ,, 6. Skull of Hyjmos subniger. „ 7- Diagram showmg the connections of the hyo-mandibular, the hyoid, and the first branchial arch with the skull in Hypnos subnig r. BY WILLIAM A. HASWELL, M.A., B.SC. 119 Fig. 8. Pectoral fin of the same. ,, 9. Pelvic arch and pelvic fin of the same. „ 10. Coalescent anterior vertebras of Trygonpastlnaca seen from below, „ 11. The same from above, a— process for articulation with the pectoral arch, b— tubercles with which the branchial arches articulate, c — nerve foramina. ,, 12. Skull of the same species. ,, 13. Pectoral arch of Crossorhinus barbatus. ,, 14. Nasal and labial (?) cartilages of Urolophus, seen in situ from the front. NOTES AND EXHIBITS. Mr. Macleay exhibited for Mr. James Macdonald, who was unable to be present, a specimen of a very curious little fish, which his nephew, Master John D. Wilson, had captured at the North Shore in an empty shell. Mr. Macleay said that it was a species of Salarias, and as far as he had been able to examine it, thought it was new. Mr. Pedley exhibited three specimens of Centriscus gracilis, an extremely rare fish in Port Jackson. WEDNESDAY, 27th FEBRUARY, 1884. The President, C. S. Wilkinson, Esq., F.G.S., F.L.S., in the chair. MEMBER ELECTED. Dr. R. von Lendenfekl. DONATIONS. A number of pamphlets, chiefly on Ornithology. By Dr. Otto Finsch. From the author. " Transactions of the Entomological Society of London." Part 4, for 1883. From the Society. "Journal of the Royal Microscopical Society." December, 1883 From the Society. "Report on the Botanic and Zoological Gardens, Singapore." For 1882. From the Government of the Straits Settlements, " Transactions, Proceedings and Report of the Royal Society of South Australia." Vol. IV., for 1882-83. From the Society. "Feuilledes Jeunes Naturalistes." No. 159. January, 1884. From the Editor. " Abhandlungen herausgegeben von der Senckenbergischen Naturforschende Gesellschaft, Frankfurt a/M." XIII Band, 1 and 2 Heft, 4to, 1883. And " Bericht," for 1882-83. From the Society. DONATIONS. 121 " On the structure and affinities of the Tabulate Corals of the Palaeozoic Period." By Dr. H. Alleyne-Nicholson. 8vo, 1879. From Professor W, J. Stephens, M.A. "Science." Volume lit, Nos. 45 to 48. From the Editor. "The Victorian Naturalist." Vol. 1, No. 1, January 1884. From the Field Naturalists Club of Victoria. " Memoir and Correspondence of Sir J. E. Smith, F.R.S., &c." 2 Vols., 8vo., 1832. From Thomas Whitelegge, Esq. PAPERS READ. A MONOGRAPH OF THE AUSTRALIAN SPONGES. By Dr. R. von Lendenfeld. 1. — Introduction. During the two years I have spent in the colonies for the purpose of investigating the Ccelenterata of our shores, I have collected and studied a great many sponges. I was entrusted with the identification of the sponges belonging to the Museums in Dunedin, Christchurch and Adelaide ; and I perform a pleasant duty in thanking the Directors, von Haast, Haake and Parker, for the great liberality with which they assisted me in obtaining the specimens and information which I sought for. The material and experience at my disposal would probably have remained obscure and useless had it not been for our Hon. Secretary, Through the well-known generosity of the Hon. W. Macleay, I shall be enabled to work out my subject exhaustively, and lay before the scientific world an extensive Monograph on my subject. Taking as a model O. Schmidt's "Spongien des Adriatischen Meeres." 122 A MONOGRAPH OF THE AUSTRALIAN SPONGES, THE NAME. The word " Sponge " is derived from the Greek (nroyyia which name was accepted by the Romans without an alteration : Spongia. The same root a-noyy is met with in most languages : sponge, spongea, spynge Anglo-saxon, spunge Old English, sponge English, spongie Old Hollandish, spons Hollandish, esponge Old French, eponge French, spogna, spognct Italian, esponga Spanish, esponja, esponga Provence. The German schwamm, Old German schwunnu, and the Norwegian Swamp are not related to the Greek word. The same is the case with the Russian gubak, Hebrew ekba and Chaldaic Akuba. Before entering into our subject, I shall give a brief account of our knowledge of the sponges, and cite the most important work s on the subject, so as to enable any one of my readers who might wish to study the sponges, to find the references he requires. It is always interesting to know, how any special science or branch thereof, has been developed, and I shall therefore give a short historic introduction, — an Embryology of Spongiology. HISTORY OF OUR KNOWLEDGE OF THE SPONGES. I. — From Aristoteles to Belon, 350 a.G — 1553. Classical Period. As in nearly every other branch of Natural Science, so we find also here the first scientific description of Sponges in Aristoteles (384 — 322 a.C.) He described three species of Ceraospongise (I) "eon fie ra>v (TTToyycov rp'ia ytvq, 6 fiev fxavos, 6 fie ttvkvos, rplros S ov koXovctlv A^tXKeiov XfTTToraros K.a\ ttvkpotcitos kcu tcr^updraros' The three sponges referred to by Aristoteles, doubtless belong to the family of the Spongidte of F. E. Schulze (2). (1). Aristoteles. 7repl fwcof laroplas. Liber V , Cap. 16., § 76. (2). F. E. Schulze. Ueber den Bau und die Entwickelung der Spongien, VII. Dit> Fainilie der Spo/iaidce. Zeitschrift fiir wissenschaftliche Zoologie Band, XXXII. BY DR. R. VON LENDENFELD. 123 Besides these, Aristoteles describes (3)., another genus, which according to O. Schmidt (4). is a Sarcotragus O. S. ; eo-n b'/IXXov yevos ov KaXovcnv dnXvcruis 8ia to pfj 8vvacrai TrXiiveo-Oai." Aristoteles mentions that the sponges contract in rough weather, so as not to be torn from the rocks by the breakers. Because they are covered with dirt when brought to the surface, he thinks that they live on organic substances, which fall on them by chance. He knew that sponges can be propagated by cuttings, a subject we shall have to dwell on in detail further on. At least he mentions that sponges, which have been broken off grow out again (5). He thought that the sponges were animals and not plants, which appears evident from the fact that he lays great stress on their similarity to plants, which of course he would not do if he thought that they were plants. Aristoteles is the only man of the ancient time whose writings on this subject are worth recording. Plinius (6), (23 — 79, p. C), Dioscorides (7), and Claudius Aelianus (8), (about 180, p. C), only copied Aristoteles' works without mentioning his name. They add to the correct statements of Aristoteles a lot of foolish myths. Present Time. II.— From Belon to Grant, 1553 — 1826. During the dark time of the middle age when the Church prosecuted and burnt all men of science, no one attempted to augment our knowledge of Biology, so that we have to pass over those ages which are a stain to humanity, from the old Aelianus 180, p. C, to Wotton, 1552, without being able to record a single paper on our subject. Full 1400 years passed away without leaving any trace in history of our knowledge of Spongidse. (3.) Aristoteles. Trepl t^mav io-roplas. Liber V., Cap. 16, § 80. (4y. O. Schmidt. Die Spongien des Adriatischen Meeres, Seite 35. (5). Aristoteles. ivepi fawv iaropias- Liber V., Cap. 16, § 77. (6), Plinius Seeundus C. Historic/, Naturalis. Liber IX. , Cap. 45. (7)- Dioscorides P. Trepl v\r]s IciTpiiajs Liber V. (8). Aelianus Claudius, Trepl ^cowir Liber VIII. Cap 16. 124 A MONOGRAPH OF THE AUSTRALIAN SPONGES, The earliest writings of the present ei-a are those of Wotton (9) (1552), and Belon (10) (1553), Both of these copied Aristoteles' writings. I will not ti-ouble the reader with a list of the names, the bearers of which wrote on Sponges at the end of the sixteenth and beginning of the seventeenth Century, some declaring them to be animals, others to be plants, and others again taking them for concentrated spray (Gerarde (11) (1633). There is a great similarity between Aphrodite and a sponge ! Of greater interest to us appears an essay of Nieremberg (12) (1635), in which for the first time we find an Australian Sponge mentioned. He says that the Hindoos call an Australian Sponge Amacpalli : " Amacpalli seu manum coccineam appellant Indi quoddam Spongiae marinae genus in Australi pelago." In Ray's (13) (1686) works, we find eight species of sponges described, which together with some Corals (Alcyonium), are placed among the fungi as " Plantae imperfectae." At that time the sponges were considered as plants, and we find several authors placing them in the vegetable kingdom. One of these authors, Tournefort (14), describes the sponges with the following diagnosis : " Herba? marina? aut fluviatiles, quarum flores et fructus vulgo ignorantur." Also the famous Anthony von Leeuwenhoek (15), appears to have held similar opinions. Carl von Linne (16), shared at first the error of his contemporaries, and described the sponges as Cryptogamic plants. (9). E. Wotton. De differentiis animalium. Liber, X.. Parish, 1552. (10). P. Belon. De Jgustibus. Liber II. Parisii, 1553. (11). T. < Jerarde. The 11, rbaU. London, 1633. (12). T. E. Nieremberg. Historia Natures. Antverpice, 1635. Liber XIII. Cap. XXXIL, p. 292. (13). T. Ray. Historiaplantarum~Loiidhu, 16S6, 1693, 1701, and Synopsis meth. stirp. Britann. Londini, 1690. (14). T. P. Tournefort. Tnstitutiones rei herb. Vol. I. Parisiis, 1700. (15). A. von Leeuwenboek. Microscopical observatio?is. Philosopbical Transactions. XXIV. (1706), p. 2158. (16). Carl von Linne\ Mora Lapponica, Amstelajdami, 1737, and Hortus Cliffort. Amstelsedami, 1737. BY DR. R. VOX LENDENFELD. 125 An essay of a much higher scientific standing than any of those mentioned above, and where we for the first time meet with higher philosophical ideas, was published by Donati (17), in 1750. According to Donati, there exists in natm'e a continuous series of living beings, so that the animal and vegetable kingdom are not separated. In his book" he lets the " Polipari " containing the sponges follow on the plants, they form the " primo grado con cui la Natura fa passagia in Mare dalle Piante agli Animali." The second grade are the " Piantianimali," which are divided into three groups. He describes some sponges very accurately, and mentions for the first time the existence of spicules, " spine di sostanza d' osso." Rnmpf (18), describes some sponges from the Banda sea, but it is not possible to identify them with our North Aus- tralian sponges with any certainty. Only one, his "Nidus vesparum marinus" I shall probably be able to identify with one of them. After Peyssonel (19) and others had been induced by worms and other animals, which sometimes live in sponges, to believe that they were produced by these commensales, Ellis (20) examined living sponges in an Aquarium, and discovered that these animals had nothing to do with the sponge, and that the sponges were animals sui generis. Besides this, Ellis (I.e.) discovered, that currents of sea water passed through the body of the sponge ; " when we examined these in glasses of sea water, we could plainly observe these little tubes to receive and pass the water too and and fro." These openings he took for the mouths of the sponge. There is therefore no doubt that he is the discoverer of the Pores and Oscula, and their func- tions. (17). V. Donati. Delia storia naturale marina dtlV Adriatko. Saggio. Venezia, 1750 (18). G. E. Rumpf. Herbar, Amban. Tom. VI. Amstselodami, 1750. (19). T. A. Peyssonel. New observations on the worms that form sponges. Philosophical Transactions. Vol. L., 2 (1758), p. 590. (20). T. Ellis. On the Nature and formation of Sponges. Philosophical Transactions. Vol. LV. (1766) p. 2S0. 126 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Our knowledge of the species of sponges was greatly increased by Pallas (21). He describes 28 species of sponges, as belonging to the genus Spongia, and there are also some sponges in his genus Alcyonium. He accepts Ellis's discoveries as correct, and places the sponges — doubtless animals — under the Zoophyta, genus Spongia. " Animal ambiguum crescens, torpidissimum. Stirps polymorpha, e fibris contexta, gelatina viva obvestitis. Oscula oscillantia (?) seu cavernse cellulaeve superficiei." In the twelfth edition of Linne's (22) Systema Naturae, the sponges are for the first time described as animals. Several species of sponges are described by authors of this period without advancing our knowledge of the Anatomy and Physiology at all. After Ellis's death, Solander set to work to publish the papers of Ellis, but he also died over the work, which was then taken in hand by Ellis's daughter. In this book (23), Ellis's and Solander's disco vei'ies are united to a whole. It contains a lot of valuable information. Alcyonium and Spongia which have hitherto been considered very nearly related, or even to be the same, are strictly separated. The genus Spongia is denned in the following manner : "Animal, fixum, flexile, polymorphum, torpidissimiun, contextum vel e fibris reticulatis, vel e spinulis, gelatina viva vestitis ; osculis seu foraminibus superficiei aquam respirans." Esper (24) and Olivi (25), who devoted much time and trouble to the sponges, did not render so much service to our Science as their English contempoi-aries. (21). P. S. Pallas. Elenchus Zoophytorum. Hagae Comit., 1766. (22). Carl von Linne. Systema Naturae. Ed. XII. Vol. 1, 2. Holmiae, 1767. (23). T. Ellis and D. Solander. Natural History of many curious and uncommon Zoophytes. London, 1786. (24). Esper. Die Pjlanzenthiere and I ortselzung der Pfla?izenthiere. Nurenberg, 1791— 1S06. (25). L. Olivi. Zooiogia Adriatica. Bassana, 1792. BY DR. R. VON LENDENFELD. 127 De Lamarck (26), who deserves our attention as a general Biologist through his work " Philosophic Zoologique," in which he expounded our present ideas of the variability of species, and of the descent of one form of animal life from another ; also devoted some of his energy to the sponges. In his " Systeme des Animanx sans Vertebres," he describes and figures 54 species, but unfortu- nately also he mixes the sponges up with the Alcyonarians. He believes, namely, that all sponges possess polypes, and that it is only in consequence of deficient observation, that they had not been seen in all species, he goes so far as to call the sponges "Polypiers." Lamouroux (27) already describes 168 species, and he, although copying Lamarck in many respects, states that the sponges are very, and fundamentally different from the Alcyonarians. His work is the best of the time. Cuvier (28) treated the sponges very superficially, and without taking any notice of the former works of Ellis, Solander, Lamarck, and Lamouroux. Of greater importance is A. T. Schweigger's (29) essay on sponges. He was the first to use the anatomical structure for classificatory purposes, and to point out the difference between calcareous and other sponges. The prevailing opinion of his time, that sponges contain polypes, which had as yet not been discovered, he treats ironically, although in consequence of the deficient methods of his time he is of course not able to prove their non- existence. He also observed the movements of the Oscula, which changed their diameter whilst he observed them. T. E. Gray (30) considered the sponges as plants, and stated, that all sponges possess spicules. His observations were made on (26). M. De Lamarck. Histoire des animaux sans vertibres. Paris. 1S16. (27). T. Lamouroux. Histoire des polypiers coralles Jiexibles. Casn, 1816. (28). G. Cuvier. Eegne animal. Vol. IV., 1817, (29). A.T. Schweigger. BeobachtungenavfNaturhirtorischenReisen. Berlin, 1S19, and Handbuch der Naturgeschichte skekttloser ungegliederter Thiere Leipzig, 1820. (30). T. E. Gray. On the situation and rank of sponges in the scale of Nature. Zoological Journal, I., 1824, p. 46. 128 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Spongilla and a few other sponges from which he thought himself justified to conclude that all sponges were Monactinellae, in Spongilla he saw green bodies, and therefore considered it as a plant. A short time afterwards, and after his ideas had been adopted by several Zoologists, Gray changed his opinion and declared the sponges to be animak. III.— From Grant to F. E. Schulze, 1826-1875. Till Grant, so little was known about the Anatomy and Phy- siology of the sponges, that it appeared advantageous to review the papers of that period in their chronological order without reference to the contents. In the period of progress initiated by Grant, a division of the papers under three headings becomes necessary, and we shall commence with the papers referring to the Anatomy and Histology of the sponges. In this branch of Spongiology, we have now happily got over the dark age ; and having worked our way through innumerable papers of little value, come to a series of publications, with which, as I can safely say, our knowledge of the sponges practically commences. The author of these papers is R. E. Grant. He states that the sponges consist of a soft mass with or without a skeleton. This mass contains throughout ramified channels, through which water is continually passing. The water enters through small holes in the surface, Pores, and leaves the body of the sponge by means of the Oscula, which our author calls faecal orifices. The current of water runs always in the same direction, and is never reversed as former authors stated. He considered swinging cilia to be the cause of the current, although he did not observe them. He says that no classification of sponges is possible without the knowledge of their anatomical structure, and states that some sponges have a fibrous skeleton, consisting of horny fibre only, whilst in others, BY DR. R. VON LENDENFELD. 129 spicules are contained in the fibres (31). He figures and describes the three forms of calcareous spicules (32). He observed the ova, the ciliated Embryo, and also, that this Embryo, after swimming about for some, time, affixes itself (33). He considers Spongilja to be nearly related to the siliceous marine sponges. (34.) Like Lamarck, Grant (35) partly indulged in the views we now call " Darwinian." Darwin says in his introduction to the " Origin of Species" that " Grant, in the concluding paragraph in his well-known paper on the Spongilla, clearly declares his belief that species are descended from other species and that they became improved in the course of modification." Nardo (36) appears to have arrived at similarly sound con- clusions as Grant, without knowledge of the latter's essays. Dujardin (37) discovered the amoeboid movement of certain cells in sponges in 1838. Laurent (38) two years later described the propagation of Spongilla very minutely. In this period we find Huxley's and Owen's names in the records of Spongiology, who, together with many other authors, are building up a good foundation for future work. Dobie (39) discovered in 1852, the cilia on all the free surfaces of a calcareous sponge. We can trace the improvements of the (31). R. E. Grant. Observations and experiments on the structure and function of the Sponge, Edinburg, Philosophical Journal. Vol. XIII., and XIV. (.32). R. E. Grant. Remarks on the structure of some calcareous Sponges. Edinburg. New Philosophical Journal. Vol. I. (33). R. E. Grant. Observations on the spontaneous motions of the ova, etc. Edinburg., New Phil. Journal. Vol I. (34.) R. E. Grant. On the structure and nature oj Spongilla fluviatilis. Edinb. Phil. Journal. Vol. XIV. (35.) R. E. Grant, (1 c). Vol. XIV., p 283. (36.) J. Nardo. Classification cler Schwdmme. Isis., 1833, 1S34. (37.) F. Dujardin. Observations sur les Sponges. Annales des Sciences Naturelles, Tom X., 1838, p. 5. (3S ) T. Laurent. Recherclies sur la Spongillefluviatile. Comptes rendus. Tome. XL, 1840, p. 1048. (39.) W. Dobie. Note on the observation oj cilia in Grantia. 1S32. Vol, X., p. 317. 9 130 A MONOGRAPH OF THE AUSTRALIAN SPONGES. Microscope very clearly in the discovery of all the minute details in the anatomy of our animals. In 1856, Lieberkiihn (40) published an excellent paper on the development of spongilla. Afterwards Carter (41) wrote on the same subject, and without being acquainted with Lieberkiihn's paper, arrived at nearly identical results. Bowerbank (42) drew in 1858, attention to the great variety or the siliceous spicules in shape, particularly those anchorate and stellate forms, which we find in some of the siliceous sponges (Stelletta O.S., Ancorina O.S., &c.) He, as Grant had done before him, considered at that time the shape of the spicules as the principal thing to be considered in classifying the sponges. We shall find that he afterwards abandoned that idea to some extent, but that the recent researches of Zittel on fossil sponges show the correctness of it. Lieberkiihn (43) extended his observation to the marine sponges, and published in 1859, an excellent paper on their anatomy. He describes the canal system and the ciliated chambers, which, as we shall see, are peculiar and all important to the sponges. Carter (44) arrived at the same time at very different results. He states that the ciliated chambers are not chambers as described by Lieberkiihn, but solid masses of cells which bear cilia on their external surface, and he points out their similarity to Volvox. In another paper (45) he dwells on the similarity of thegemmuke of Spongilla, to the winter ova of many simple algae ; and states that they contain starch granules. (40.) N. Lieberkiihn. Beitrage zur Entwickelungsgeschichte der Spongillen. Miillers Archiv., 1856. (41.) H. Carter. On the ultimate structure of Spongilla, Ann. Mag. Vol. XX. (1857), p. 21. (42.) Bowerbank. On the Anatomy and Physiology of the Spongida. Trans. Roy. Soc., Vol 148, p. 279. (43.) Lieberkiihn. A'twe Beitrage zur Anatomic der Spongien. Archiv. fiir Anatomie und Physiologie, 1859. (44.) Carter. Ann. Mag., Vol. III. (1859), page 12. (45.) Carter. Ann. Mag., (1859), Vol. III., p. 331. BY DR. R. VON LENDENFELP. 131 In 1860, Max Schultze (46) published a paper on Hyalonrma, which at that time, when deep sea dredging was unknown, was very rare, and described it as the skeleton of a sponge affixed to the bottom of the sea by the long glassy threads which grow out from one extremity of it. By many nativralists the Hyalonemas were considered as artificial products, made by the Japanese out of glass. Ehrenberg (47) held that opinion amongst others, and attempted to prove the inefficiency of Schultze's paper. In the subsequent contro- versy the animal nature of these Hexactinellid sponges was proved, although Ehrenberg himself never acknowledged that he had made a mistake. With the year 1862 we enter into the modern and most fruitful period of the study of sponges, and we can safely say that everything published before that year, since Aristoteles, is not of such value as the discoveries made in every one of the years, from 1862 to 1884. Bowerbank (48) publishes a series of valuable observations on the Anatomy of the sponges, and dwells in detail on the spicules, which are accurately figured and described. Lieberkiihn (49) continues his observations on Spongilla ; among the important results of his investigations, I will mention the fact, that he thinks he has observed, that the ciliated Embryos of Spongilla sometimes multiply by fission, a statement of great importance. Kolliker gives a preliminary notice of his histological investiga- tions, in the same year. A full account of this most important (46) Max Schultze. Die Hyalonemen, ein Beitrag zur Kcdurgeschichte der Spongien. Bonn., 1S60. (47-) (J. Ehrenberg Bertrage zur Beuriheilung der Gattung Hyalonema. Monatsberichte der Akadem. Berlin I860, p. 173. (48). T. J. Bowerbank. On the Anatomy and Physiology of the Spongiadce. Phil. Trans. Roy. Soc. Vol. 148, p. 279. Vol. 152, p. 830. Vol. 152, p. 747- Arol. 152, p. 1082. (49). N. Lieberkiihn. Ueber Beicegungserscheinungenbei den Schvximmen. Midlers Archiv., 1863. Seite, 717. 132 A MONOGRAPH OF THE AUSTRALIAN SPONGES, work (50) appeared two years later. Kollikers observations on the Histology of the Sponges, can be considered as the foun- dation of our present knowledge of that subject. He discovered fibrous cells which he correctly considers as muscles. He pointed out that the horny skeleton of many sponges, as well as the calcareous and siliceous spicules are to be considered as productions of gland cells, and grow by apposition, a statement which has recently been proved by F. E. Schulze (51) and myself (52). He observed in many cases a cuticle on the surface of the sponges in continuity with, and of the same substance, as the horn fibres. The correctness of this observation was doubted by F. E. Schulze (1. c.) I have been able (1. c.) to prove that Kolliker's statements on this point are perfectly correct, because, as we shall see hereafter, sponges attain such a cuticle, when sick ; and it is highly probable that Kolliker had studied only sponges that had not been treated with the modern refinements of histological investigation. F. E. Schulze's statement that such a cuticle does not exist is perfectly correct for the healthy living sponge, and for specimens treated in such a manner that they are killed before they have time to get sick. O. Schmidt (53) published in 1865 his first supplement to the Adriatric Sponges, in which his views on the Histology are expressed. They differ from those of Kolliker. Lieberkuhn (54) dwells on the anatomical structure of the calcareous sponges. He described in 1865 the configuration of the canal system very accurately. (50). A. von Kolliker. Icones Histologics, 1. Abtheilung Protozoen Leipzig, 1869. (51). F. E. Schulze. Ueber den Bau und die Erttwichelung cler Spongien. DieFamilii der Spongidae. Z f. w. Z. Band 32, Seite, 593. (52). R. von Lendenfeld. Ccelenteraten der Siidsee II., Neue. Aplysinidce. Z. f. w. Z Band 38. Seite, 234. (53). 0. Schmidt. /. Supplement zu den Spongien des Adriatischen Metres, 1864. (54). N, Lieberkuhn. Beitrage zur Anatomie der Kalkspongien. Midler's Arc hi v., 1865, p. 732. BY DR. R. VON LENDENFELD. 133 In the still continuing dispute between M. Schultze and Ehrenberg, about the root of Hyalonema, Bowerbank (55) enters with the statement, that the apertures (Cloaca) were to be found at the base of the sponge. He declares, namely, the Coral (Polythoa) which generally overgrows the Hyalonema, as part of the sponge, and considers the holes in it — where the Polypes had been situated — as the Oscula of the Hyalonema. Haeckel (56) published in 1870 his observations "liber die sexuelle Fortpflanzung und das natiirliche System der Schwamme'' whex'e he describes the Spermatozoa, the fructification of the ovum and the early stages of development of the embryo. Classification and systematic position. Just as Grant opened up the Anatomy and Physiology, Johnston (57) laid the foundation for the classification. During twenty years his " History of British Sponges and Lithophytes," was the main work of reference on our subject, and has only been surpassed by the recent monogi'aphs of Bowerbank and O* Schmidt. The excellent plates in this work were drawn by Mrs. Johnston. In this period we meet also with the first essays on sponges by Bowerbank (58) and Carter (59), the latter of whom is the Nestor among the present spongiologists. Carter was at that time surgeon in Bombay, and described some Indian fresh water sponges. Leukart, (60) whose classical works in other branches of zoology make his opinion valuable, already in 1854 pointed out, that the (55). T. Bowerbank. Hyalonema mirabile. Proc. Zool. Soc, 1867, p. IS' 350. (56). Ernst Hseckel. Ueber die sexuelle Fortpflanzung unci das natiirliche System der Schwamme. Jenaische Zeitschr. VI. Seite. 641. (57)- G. Johnston. History of British Sponges and Lithophytes. Edin. 1842. (58). J. S. Bowerbank. Observations on a Keratous Sponge, from Australia. Ann Mag., Vol. VII. (1841), p. 129. (59). H. T. Carter. Notes on the species of the freshwater Sponges of Bombay. Ann. Mag., Vol. I. (1848), page 303. (60). R. Leukart. Archiv. fin. Naturgeschichte, Band II. 134 A MONOGRAPH OF THE AUSTRALIAN SPONGES, sponges were related to the corals and hydroids, of course in a very different sense from that in which Lamarck and his con- temporaries united them with the Alcyonarians. Althoughthese views have been disputed ever since, all men of science of the present day nearly agree to the correctness of Leukart's statement. Huxley (61) at that time considered the sponges to be colonies of Protozoa, and called them " unicellular " organisms. In the sense which Huxley applies to the word " unicellular " all animals would have to be termed so, because all can be considered as colonies of simple cells — Protozoa. in the same year Gray (62) described, among others, two sponges, Carpenteria and Dujardinia, which, according to Gray, hold an intermediate position between the sponges and the Poly- thalamia. Lieberkiihn (63) classifies the sponges according to the anatomy of their skeletons, and divides the whole of the sponges, in the way Grant had insinuated, into four groups : Halisarcina, without skeleton ; Spongina, with a skeleton, consisting of horny fibre ; Calcispongina, possessing spicules composed of carbonate of lime, and Halichondria possessiug spicules composed of silica. This classification has been adopted, more or less, by Bowerbank and O. Schmidt, and has been taken by Zittel, whose classification is now almost universally recognized, as the foundation of his own system. In 1862, 0. Schmidt (64) published his well-known " Spongien des Adriatischen Meeres," and described and figured very accurately a great many species from the Adriatic ; since then for the last 22 years he has devoted all his time to the systematic description of sponges, and the study of their genetic relationships. (61). T. Huxley. Zoological notes and observations. Annals and Magazine of Natural History, 1851, Vol. VIII., p. 370; 1851, Vol. VIII. , p. 433. (6-2). G. Gray. Desc iption of Aphroceros . Proc. Zool. Soc, Vol. XXVI., p. 1 14. (63). N. Lieberkuhn. Neue Beitragczur Anatomie der Spongien. SI tiller's Aivhiv., 1859, Beite, 353, 515. (GIJ. 0. Schmidt. Die Spongien des Adriatischen Meeres, Leipzig, 1862. BY DR. R. VON'LE^DENFELD. 135 The classification is the following : — I. Calcispongice (according to Grant — Lieberkiihn.) II. Ceraospongice (Spongina Lieberkiihn). III. Gummince (without continuous skeleton and tough like india- rubber, containing Nardo's Chondrosia). IV. Corticatcv (siliceous sponges, possessing as the term implies, an outer layer different from the interior of the sponge). V. Halichondrice (according to Lieberkiihn), and VI. Halisarcina (according to Lieberkiihn). In the same year appeared Bowerbanks (65) preliminary report on the Classification of the British Sponges, in which he adopts Grant's Classification. He calls the three groups : Calcarea, Silicea and Keratosa. In 1864 appeared the first volume of Bowerbank's " Monograph of the British Sponges." (66). The skeletons of many sponges are carefully described and many spicules are figured. He uses the classification published by him in the preliminary report mentioned above. The usefulness of this work is greatly impeded by the authors extraordinary neglect of other papers on the same subject. Several of the most important works on sponges, published shortly before, he does not appear even to have read. Duchassing and Michelotti (67) described a number of new sponges from the Carribean Sea. Unfortunately they noticed neither the works of Bowerbank nor those of O. Schmidt, so that many of their species are identical with sponges described before. Fritz Miiller (68) discovered in 1865 an extraordinary sponge in South America, which possesses horay star shaped spicules. One of the species described by myself (69) from Australia (65). T. Bowerbank On the A natomy and Physioloqy of the Spongidce. Trans Phil. Soc , 1862. Vol. 152, p. 10, 87- (66.) J. Bowerbank. A Alonoqraph of the British Spongidce. Ray Soc, London, 1864. (67). Duchassing et Michelotti. Spongiaires de la mer C'araibe. Natur- kundige Verhandlungen Maatschaappij Haarlam. XXI., 2 (1S64), p. 7. ( 68). F. Miiller. Ueher Darwinella aurea. Archiv. fiir mikroskopische Anatomie Band, I. Seite, 344. (69). R. von Lendenfeld. Ueber Coelentenden des Sihlsee II. Neue Aplysinidse. Zeitschrift f. wiss. Zool. Band. XXXVIII. Seite, 234. 136 A MONOGRAPH OF THE AUSTRALIAN SPONGES, contains fibres with a star shaped transverse section, and helps as I pointed out in the place cited above, to explain the otherwise unprecedented occurrence of such Keratous stars. Up to 1866, all Zoologists had, with the abovenauied exception of Leukart, considered the sponges as Protozoa. Amongst others, Huxley, O. Schmidt, and Kolliker. At the Versammlung deutscher Natnrforscher und Arzte at Hannover, in 1866, Van Beneden and Claus declared the sponges to be Ccelenterata (70). In consequence of Bowerbank not making use of previously published essays, a great confusion in the nomenclature arose. 0. Schmidt therefore in his second Supplement (71) reduced the diagnoses of Bowerbank to his own names, and it is only with this key possible to understand Bowerbank's work. In the same year appeared the second volume of Bowerbank's Monogi-aph (72). A year later Hancock (73) published a paper on excavating sponges, to prove that they were not as Bowerbank had stated, ordinary Halichondrise, which lived in deserted worm tubes, and other old excavations, but that they bored these holes themselves. In 1867, Selenka (74) published a paper on the sponges of th Southern Seas, where for the first time a number of Australian sponges are accurately described and figured. I have been able to identify several of our sponges with Selenka's species. (70). Amtlicher Bericht der Versammlung deutscher Naturforscher und Aerzte in Hannover, 18G6. (71). 0. Schmidt. Zweites Supplement zu den Spongien des Adriatiscken Meeres. Leipzig, 1866. (72). J. Bowerbank. A Monograph of the British Spongidee Vol. II. Roy . Soc, London, 1866. (73). A. Hancock. Note on the excavating sponges. Ann. Mag., 1867, Vol. XIX., p. 229. (74). E. Selenka. Tiber einege neue Schwdmine der SUdsee. Z. f. wiss. Zool. Band XVII. Seite, 565. BY DR. K. VON LENDENFELD. 137 In 18G8, two eminent Zoologists, Haeckel (75) and Miklouho- Maclay (76) tried to prove the correctness of Leukart's (1. c.) opinion, that the sponges are Coelenterata. Haeckel arrives at the opinion of the Ccelenterata-nature of sponges, by his extensive knowledge of a great many species ; whilst Miklouho-Maclay (1. c.) was brought to this view of the subject by the intensive study of a single form Guancha blanca. The most important point in this question, is the fact, that the sponges are developed like all higher animals from ova and Sper- matozoa, and pass through a Gastrula stage, wherefore they must be strictly separated from the Protozoa. It is Haeckel to whom the merit of pointing out this simple but all important fact is due. Gray (77) published in the same year a classification of the sponges, which has not been accepted by the scientific world. He also describes several new species from Australia. Bowerbank (78) criticised Gray's system rather shai'ply, and pointed out many doubtful statements in it. In the same year, 1868, appeared 0. Schmidt's (79) third Sup- plement to his Adriatic Sponges, in which the sponges of Algeria are described. Some changes are made in the classification and new families are added. One of these, the Chalinea, is of interest to us, as nearly half of the Australian sponges belong to it. (75). E. Haeckel. Ueber die sexuelle Fortpflanzung und das natiirliche System der Schwamme. Jen. Zeitschr. VI., 641. (76). Miklouho-Maclay. Beitrage zur Kenntniss der Spongien I. Jen. Ztschr., IV., 221, aucl Ueber Schwamme des nordlichen stillen Oceans und der Eismeeres. Mem. Acad., Petersbourg, XV., 3. Seite, 1. (77). T. Gray. Notes on the arrangement of sponges with the description of oj some new genera Proc. Zool. Soc, 1867, p. 492. (78) J. Bowerbank. On Mr. Gray's arrangement of sponges. Proc. Zool. Soc, 1868, p. 118. (79). 0. Schmidt. Ill.tes Supplement. Die Spongien von Algier. 138 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Several smaller papers on new sponges, mostly English, were published at that time. Bowerbank (80) and Claus (81) studied the Hexactinellid sponges, and particularly by the latter monograph of Euplectella aspergillum gives a correct and complete account of the skeleton. Loven (82) and others also worked on the same subject. As there are hardly any Hexactinellid (one) sponges on the shores of Australia, it is not worth while for us to enter into the history of their study more minutely. The works of Haeckel (l.c.) created, after they had been trans- lated into English, (83) I may say, a storm of indignation in England, and particularly in America, and a whole host of writers took up their pens to prove that Haeckel's and Miklouho-Maclay's views on the Ccelenterate-Nature of sponges were incorrect and ridiculous. Only Ray Lancaster (84) agreed with Haeckel. Carter (85) and Kent (86; were foremost in the combat. Also in Germany some opponents were found. Ehlers, (87) for instance, was not inclined to agree with Haeckel. Ehlers (88) re-described the sponges which were studied by Esper. In his most important work Grundziige einer Spongienfauna des Atlautischen Gebietes, O. Schmidt (89) publishes the results (80;. J. Bowerbank. Hyalonema mirabile. Proc. Zool. Soc , 1867, p. IS, 350. (81). C Claus. Ueber Euplectella aspergillum. Marburg unci Leipzig, 1868. (82). S. Lov6n Om en marklig i Nordijon lefvande Art of Spongia. Oefversight of Vetensk. Akad. forhoncllgr XXV,. p. 105. (83) E. Haeckel. On the systematic position of sponges. Ann. Mag., Vol. V , 1, 107. (84.) Ray Lancaster. On the affinity of sponges. Ann. Mag., Vol. VI., p. SO. (85). H.Carter. On the ultimate structure of marine sponges. Ann. Mag., Vol VI., p. 329. (86). S. Kent. Haeckel on the relationship of the sponges to the corals. Ann. Mag., Vol. V., p. 204. (87). E. Ehlers. Ueber Aulorhipis elegans, Z.f.w.Z., Vol. XXL, p. 540. (88). E Ehlers. Die Esperschen Spongien. Programme Erlangen, 1870. (89). O. Schmidt. Gfrundziige einer Spongienfauna des Atlantischen Gebietes. Leipzig., 1870. BY DR. R. VON LENDEMPELD. 139 of his study of the Sponges in the Museums of Copenhagen and Cambridge Mass. His classification, which he calls " Descendenz- Sjstematic," is different to most of the former classificatory systems. He tries to form continuous series instead of describing distinct species, and so breaks with the old dogmatic idea of species. O. Schmidt (90) also extends his identification of the Bower- bankian Sponges, so that only few of them retain their former incognito. He now divides the sponges into four groups : — 1. Sponges with hexaradiate spicules to which belong the fossil Ventriculites. 2. Sponges with anchor-shaped tetraradiate spicules related to the fossil Vermiculates. 3. Sponges with biradiate spicules to which belong the horn-fibred sponges, and those which possess no skeleton. 4. Calcareous Sponges. This classification has recently been adopted and worked out in detail by Zittel, (91) who supported this classification by the results of his study of fossil forms. A whole series of small papers of this period are again devoted to the Hexactinellidse. An important paper was published in 1871, by Miklouho- Maclay (92), on Veluspa polymorpha, a sponge belonging to O. Schmidt's Chalinidse. A continuous series of different forms are described, which are not divided from each other by sharp boundary-lines, and at the ends of the series we meet with totally different forms. The single individual varies to a gi'eat extent, and not even the shape of the spicules is constant. Size and colour vary very much, and different shapes of the whole are formed by different modes of concrescence of single zooids. (90). 0. Schmidt 1 c. Seite., 76. (91). K. Zittel. Zur Stammesgescluchteder Sponqien. Miinchen, 1S78. (92). Miklouho-Maclay. Veluspa polymorpha. Mem. Acad. Im Petersb., 1870, Vol XV-, p. 3. 140 A MONOGRAPH OF THE AUSTRALIAN SPONGES, It is remarkable that in the Australian waters, sponges corres- ponding to Miklouho-Maclay's descriptions are very common, and that this sponge is just as polymorphic here as Miklouho-Maclay's specimens from the White Sea. Among the thousands of Australian sponge individuals I have examined nearly the half correspond to Yeluspa Miklouko-Maclay. He also (I.e.) dwells on other sponges of varying shape. In the same year Harting (93) described Poterion, the giant among sponges. Carter (94) describes several new species. In 1872, Pagenstecher (95) published a historical introduction to our knowledge of the spongida. In the same year appeared Haeckel's Monograph of the Calcareous Sponges (96) in three volumes, with 60 plates. He hopes by the accurate study of one group of animals to render " den analytischen Beweis von der gemeinsamen Descendenz aller, einer solchen Gruppe zugehorigen Species." This well-known work may be considered as a model of a scientific zoological book. The philosophical deductions are clever, often brilliant, the classification is simple and clear, and the plates show the artistic sense of the author. The scientific facts contained therein are similar to those published previously by the same author. Whilst this publication settled all doubt about the Coelenterate- nature of the sponges in Germany ; English and American authors continue to publish papers to prove that the sponges are Protozoa. Carter (97) calls the cells in the walls of the ciliated chambers (93). P. Harting. Memoire sur cle ginre Poterion. Naturk. Verhandel- Utrechtsch. Genoatsch 1870, p. 1 . (94). H. Carter. Ann. Mag. (Series 4), Vol. VIII, p. 1 ; Vol. VIII., p. 99 ; Vol. IX., p. 409 ; Vol. XII., p. 349. (95). H. Pagenstecher. Zur Kenntniss der Schwdmme I. Geschichtliche Einleitunij . Verhandl. Verein Heidelberg VI., 1872, Seite. 1. (96). E Haeckel. Die Kalkschwamme 3 Biinde, Berlin, 1872. (97). H. Carter. Developement of the Murine tiponyes. Ann. Mag., Vol. XIV., p. 321, 3S9. B¥ DR. R. VON LENDENFELD. 141 Spongozoa, he observed that they copulated like Difflugia, and in this way sexual multiplication was attained. The embryos formed by the conjugation of two Spongozoa are developed in the canals. He observed (I.e.) that carmine particles were absorbed by the Spongozoa and digested by them, which he takes as a proof that these cells are really animals kut i^oxf}v. According to that the epithelium of the intestine of higher animals which also absorbs carmine must likewise be considered as a colony of many separate animals. He comes to the conclusion that the ciliated chambers are more like Ascidians than Polyps. At the conclusion of another paper (98) he gives his view on the subject in the following words: — "The Spongozoan must, ipso Jacto, be con- sidered the expression of the sponge, in so far, that it represents the stomach and the generative apparatus, aided by the rest of the body, which thus becomes analogous to such accessories in the highest animals, although the plurality of Spongozoa scattered through the mass may more nearly resemble in this respect the flower buds of plant, such then appears to be the nature of a sponge." Paleontology. After our knowledge of the fossil sponges had been gi'eatly increased by Goldfuss (99), de Blainville (100), made the first attempt to unite the fossil and recent sponges in one classificatory system. Toulmain Smith (101) published in 1848, an excellent mono- gragh of the cretacious Ventriculites. He describes the spicules very accurately. Regarding the systematic position of those Ventriculites he made a mistake. He declares them to be Polyzoa. (98). H. Carter. On the nature of the side-like body of Sponqilla &c. Ann. Mag., Vol. XIV., p. 97. (99). G. Goldfuss. Petrefacta Germanics. Diisseldorf, 1826-1833. (100). M. De Blainville. Article Eponge. Dietionnaire des Sciences Naturelles, 1819, Vol. XV. (101). Toulmain Smith. On the Ventriculidce of the chalk. Ann. Mag Vol. XX., (1847), p. 73. S 142 A MONOGRAPH OF THE AUSTRALIAN SPONGES, IV. — FromT. E. Schultze to the present day, 1875 — 1884. Tn no branch of Biology has such an advance been made within the last ten years as in Spongiology. The papers to be mentioned here shall be reviewed more briefly than the preceding ones, because we shall have to repeat their contents anon : we cannot write a history of a period which is not completed. We shall have to divide the papers of this period into five groups, and shall commence as in the foregoing chapter with the Anatomy. Anatomy and Histology. In a series of papers (102) Schultze describes very accurately many genera of sponges belonging to several different groups. His results are in the main features the following : — The sponges consist of three layers Ectoderm, Entoderm, and a third, which he hesitatingly calls Mesoderm. The Ectoderm consists throughout of simple flat ciliated cells, which cover the outer surface of the sponge, and the walls of the canals through which the water flows from the outer surface to the ciliated chambers. These ciliated chambers, together with the canals leading from thence to the Oscular tube, and also this tube, are covered with Entoderm al cells, which in the chambers of the ordinary, and in the corresponding tubes of the calcareous sponges, have the shape of long, fringed and ciliated elements, whilst in the canal system they (102). F. E. Schulze. Ueber den Ban und die Entwiclcelung der Spongien. Zeitschrift fiir wissenschaftliche Zoologie. Sycandra ray nanus Supplement, Band, XXXV., Seite, 247. Entwickelungsgeschichte von Sycandra. Band, XX VII., Seite, 486. Die Gattung Halisarca, Band, XXVIII., Seite, 1. DieFamilie der Chondrosidse, Band, XXIX., Seite, 87- Die Familie der Aplysinidse, Band, XXX., Seite, 379.' Metamorphose von Sycandra, Band, XXXI., Seite, 262. Die Gattung Spongelia, Band, XXXII., Seite, 117. Die Familie der Spongidse, Band, XXXII. , Seite, 593, Die Gattung Hircinia Hand, XXXIII., Seite, 1. Die Plakiniden, Band, XXXIV., Seite, 407. Cortichvm candelabrum, Band, XXXV., Seite, 410. BY DR. R. VON LENDENFELD. 143 form a low ciliated Epithelium. The intermediate layer which forms the bulk of the sponge, consists of a soft gelatinous or harder cartilaginous substance, like the gallert of the umbrellas of the Medusae, in which cells of different shapes are embedded. These cells are partly elongate, muscular, partly star shaped tissue cells, partly horn-producing, gland cells, ova, spermatophors, and so on. Keller (103) and Metschnikoff (104) agree in the main points with Schulze. Schulze (105) describes a new form of propagation of sponges, by floating polycellular buds. Sollas (106) made experiments to show the influence of caustic potash on the spicules ; he published a series of anatomical and histological researches, which contain a great many interesting facts, and are worthy of comparison with Schultze's classical works. Also, Carter (107) published some data on the structure of sponges, but unfortunately without noticing the previous publica- tions on the subject. Schulze (108) published in 1881, a paper on the soft parts of Euplectella, from which we learn, that the Histology of this well- known sponge, corresponds with the minute structure of sponges belonging to other groups. (103). O. Keller. Untersuchung ilber die Anatomle und Entioichelungs- geschichte einiger Spongien des Mittelmeeres. Basel, 1S76. Ueber den Ban von Meniera semitubulosa. Z. f. w.Z., XXX., Seite,563. Studien ilber Organisation und Entwiclctlung der Chalineen. Z. f. w. Z., XXXIII., 317. Neue Coelen- enteraten aus dem Golfe von Neapel. Arch. f. mik. Anat. XVIII., 271. (104,). E. Metschnikoff. Beitrdge zur Morphologie der Spongien. Z, f. w. Z. Baud. XXVII., Seite, 275. Spongiologische Studien. Seite, 349. (105). F. E. Schulze. Ueber die Bildung freischwebender, Brutknospen bei einer Spongie Halisarca lobularis. Zool. Anz. II., Seite, 636. (106). Sollas, Sp>onge fauna of Norway. Ann. Mag (Series 5), Vol. V., p. 130. Vol. V., p. 241. Vol. V., p. 396. Vol. IX., p. 141. Vol. IX., p. 426. (107). H. Carter. Contributions to our knowledge of the Spoibjida II., Ceratina Ann Mag., Vol. VIII., p. 101. On the development of the fibre in the Sx>ongida. Ann. Mag., Vol. VIII., p. 112. (108). F. E. Schulze. Of the soft parts of Enplectella aspery ilium. Trans. Roy. S., Edinburgh., XXIX., p. 636. 144 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Ray Lankaster (109) dwells en Chlorophyll and Amyloid deposits in Spongilla. I published a short note on the growth of the Hornfibres of sponges (Aplysinidse) (110). Polejaeff (111) dwells in detail on the Spenna und Sperma- togenesis in Sycandra raphanns. In another paper (112) I gave the results of my researches on three species of Australian Aplysinida3. Besides endorsing Schulze's discoveries, I was enabled to draw attention to some new facts concerning the structure of sponges. Gland cells producing a slimy covering on the surface of the sponges when in unfavourable circumstances, similar to those discovered by Merejkovsky (112a) in Halisarca, were described. The formation and growth of ova and spermatozoa were studied, and several doubtful points elucidated by my researches. Classification and Systematic Position. Continuing from page 141, we record the following papers on this subject. Gray (113) publishes a classification of the sponges amended in another paper. (114). (109). Kay Lankaster. On the Chlorophyll-corpuscles and Amyloid deposits of Spongilla and Hydra. Quart. J. Micr. Sc, Vol. XXII., p. 229. (110). R. von Lendenfeld. Das ffornfaserwachsthum der Aplysinidce. Zoologischer Anzeiger. Band V., Seite. 634. (111). N. Polejaeff. Ui bt r das S/> rma und die Spermatogenese bei Sycandra raphanus. Sitznngsberichte der k. Akad. Wise. Wien. Math, nat Classe I. Abth. 86, Band 3 5 Heft., Seite. 276—298. (112). K. von Lendenfeld. Ueber Ccelenteraten der Siidsee. II. Neue Aplysinidce, Z.f.w.Z. Band XXXVIII., Seite. 234. (112a). Merejkovsky. Etudes sur les Epong dela mer blanche. Mem.de VAcad, de Petersbg., 1S78. (113). J. Gray. On the classification of Sponges. Ann. Mag. (Series 4), VTol. XL, p. 442. (114). J. Gray. On the arrangement of Sponges. Ann. Mag., Vol. XIIL, p. 284. BY DR. R. VON LENDENFELD. 145 Veiy different from this is Carter's (115) classificatory system. He divides the sponges, according to the structure of their skeleton, into 8 orders : — I. Cccrnosa, without evident skeleton. II. Ceratiaa. Possessing a skeleton composed of horny fibre, with a granular, chiefly hollow core, containing for the most part no foreign bodies. III. Psammonemata. Possessing a skeleton composed of solid fibre, more or less cored with foreign bodies. IV. Rcvphidon&mata. Possessing a skeleton composed of horny fibre, with a core of proper spicules. V. Echinonemata. Possessing a skeleton composed of horny fibre, cored with proper spicules internally, and echinated with proper spicules externally, YI. Holorlia-phidata. Possessing a skeleton, whose fibre is almost entirely composed of proper spicules, bound together by a minimum sarcode. VII. Hexactinellida. Possessing a skeleton composed of hexactinellid spicules. VIII. Calcarea. Possessing a skeleton composed of calcareous spicules. Of Bowerbank's Monograph the third volume (116) appeared in 1874, in which new species are described, and some of O. Schmidt's sponges are compared with the author's descriptions. In another series of papers (117) he describes a number of new species from all parts of the world. A great many of these are Australian. (115). H. Carter. Notes introductory to the study and classification of Spongida. Ann. Mag. (Series 4), Vol. XVI., pp. 126, 127. (116). J. Bowerbank. A Monograph of the British Spongidce. Vol. III., P^ay. Soc, London, 1874. (117 J. J. Bowerbank. Contributions to the general history of the Spongidai. Proc. Zool. Soc,. Vol. 1S72, p. 115 ; 1872, p. 156 ; 1872, p. 626 ; 1S73, p. 3 ; 1873, p. 319 ; 1874, p. 298 ; 1875, p. 281 ; 1876, p. 76S. 10 146 A MONOGRAPH OF THE AUSTRALIAN SPONGES, O. Schmidt (118) published a most important paper on the sponges of the Gulf of Mexico, where the views expressed by the same author in his paper on the Atlantic Sponge-fauna are carried out. The sponges described are throughout siliceous deep sea- sponges : Lithistida? and Hexactinellida3. In the preface we find some notes concerning Bowerbank, who, although being personally acquainted with 0. Schmidt, seems to have remained ignorant of the contents of 0. Schmidt's papers on sponges. Hyatt (119) describes many new American sponges, mostly Ceraospongia?. It would lead too far to review here all the papers containing descriptions of new species, suffice it to note a few of the more important publications of this kind. The most prominent authors in this field are the following : — Marenzeller (120), Carter (121), Higgin (122), Czerniavsky (118). 0. Schmidt. Die Spongien des Meerbusens von Mexico. Jena., 1878-80. (119). A. Hyatt, Revision of North American Porifera. Mem. Bost. Soc, Vol. L, 1875, p. 399 ; Vol. II., 1877, p. 505. (120). E. von Marenzeller. Coelenteraten etc. cler osterreichischen Nordpol Expedition. Deuschr. Akad. Wien XXXV. (121). H. Carter. Description and figures of deep sea sponges. Ann. Mag., Vol. XVII [.., 226, 307, 3S8, 458. Arctic and Antarctic sponges. Ann. Mag., Vol. XX., p. 38. On Tedania Ann. Mag., Vol. II. , p. 35. Contributions to our knozvledge of the Spongida. Ann. M., Vol. III., p. 284, 343 ; Vol. VIII., p. 101, 241. HUtory and classification of the knoion species of Spongilla. Ann. Mag., Vol. VII , p. 77- Report on specimens astoris. (Maench.) Camelina. 12. C. dentata. (Pers.) LlNEiE. LlNUM. 13. L. Gallicum. (L.) BY AV. WOOLLS, PH.D., F.L.S. 193 GERANIACEjE. Pelargonium. 14. P. graveolens. (Ait.) . Erodium. 15. E. moschatum. (Willd.) OXALIS. 16. 0. cemua. (Thunb.) MALVACEiE. Malva. 17. M. rotundifolia. (L.) 18. M. parviflora. (L.) 19. M. sylvestris. (L.) Cristaria. 20. C. coccinea. (Pmsh.) Sid a. 21. S. rhoriibifolia. (L.) EUPHORBIACEiE. Euphorbia. 22. E. peplus. (Willd.) 23. E. helioscopia. (Willd.) RlCINUS. 24. R. communis. (Willd.) UrTICACEjE. Urtica. 25. U. dioica. (L.) 26. U. wens. (L.) 194 plants which have become naturalized in n. s. w., Cannabinace^e. Cannabis. 27. 0. saliva. (Willd. C'ARYOPHYLLE.flE. Gypsophila. 28. G. tubulosa. (Boiss.) Silene. 29. S. Gallica. (L.) Cerastium. 30. C. vulgatum. (L.) Stellaria. 31. S. media. (L.) Spergula. 32. S. arvensis. (L.) Dianthus. 33. D.prolifer. (L.) POLYCARPON. 34. P. tetraphyllum. (L.) (?) PORTULACA. 35. P. oleracea. (L.) (?) AMARANTACEjE. Amarantus. 36. A. panicidatus. (L.) 37. A. blitum. (L.) 38. A. viridis. (L.) BY W. WOOLLS, PH.D., F.L.S. 195 RlJMEX. 39. R. crispus. (L. ) 40. R. conglomerates. (L.) 41. R. acetosella. (L.) Salsolace^e. - Chenopodium, 42. C. rmirale. (L.)i 43. C. ambrosioides. (L.) Atriplex. 44. A. patula. (L.) FlCOIDEiE. Opuntia. 45. 0. Tana. (Mill) 46. O.Jicus indica. (Haw.) 47. 0. vulgaris. (Mill.) Polygonace^e. Polygonum. 48. P. aviculare. (L.) 49. P. orientals. (L.) PlIYTOLACCEiE. Phytolacca. 50. P. octandra. (L ) LEGUMINOSvE. Argyrolobidm. 51. A. Andrewsianum. (Stead.) Medicago. 52. M. sativa. (L.) 53. M. lupidina. (L.) 54. M. macidata. (L.) 55. M. denticidata. (L.) 196 plants which have become naturalized in n. s. w., Trifolium. 56. T. jyratense. (L.) 57. T. repens. (L.) VlCIA. 58. V. sativa. (L.) 59. V. hirsuta. (L.) Lotus. 60. L. tetragonobohis. (L.) Ulex. 61. U. Europanut. (Willi) Cajanus. 62. C. bicolor. (D.C.) Melilotus. 63. M. parviflora. (Desf.) Eobinia. 64. E. pseudacacia. (Willd.) EOSACEiE. Eosa. 65. R. rubiginosa. (L.) ONAGREiE. (ENOTHERA. 66. 0. biennis. (L.) 67. 0. tetraptera. (Willd.) Epilobium. 68. E. roseum. (Sm.) BY W. WOOLLS, PH.D., F.L.S. 197 UmBELLIFERjE. Ammi. 69. A majus. (L.) SlUM. 70. S. latifolium. (L.) 71. S. angusti folium. (L.) Pastinacia. 72. P. sativa. (L.) Anethum. 73. A. fceniculum. (Willd.) BtJPLEURUM. 74. B. rotundifolium. (Willd.) DlPSACACEjE. SCABIOSA. 75. S. atropurpurea. (Willd.) Passiflore^e. Passiflora. 76. P. ccerulea. (Willd.) Composite. Centaurea. 77. C. Melitensis. (L.) 78. C. calcitrapa. (L.) Carthamnus, 79. C. tinctorius. (L.) Onopordon. 80. 0. acanthium. (L.) 198 PLANTS WHICH HAVE BECOME NATURALIZED IN N. S. W., ClRSIUM. 81. C. lanceolatum. (Scop.) Carduus. 82. C. Marianus. (L.) EUPATORIUM. 83. E. cannabinum. (L.) Erigeron. 84. E. Canadensis. (L.) 85. E. linifolius. (L.) Aster. 86. A. dumosus. (Willd.) Xanthium. 87. X. spinosum. (L.) Tolpis. 88. T. barbata. (Willd.) Stegesbeckia. 89. S. orientalis. (L. ) G-alinsogea. 90. G. parviflora. (Cav.) BlDENS. 91. B.jrilosa. (L.) Tagetes. 92. T. glandidifera. (Schranck.) Anthemis. 93. A. cotula. (L ) by w. woolls, ph.d., f.l.s. 199 Chrysanthemum. 94. C. segetum. (L.) 95. C. Parthenium. (Pers.) SOLIVA. 96. S. anthemifolia. (B. Br.) GNAPHALIUM. 97. G. luteo-album. (L.) 98. G. purpureum. (Thunb.) Senecio. 99. S. scandens. (D.C. ) 100. vulgaris. (L.) Cryptostemma. 101. C. calendulaceum. (E,. Br.) Hypoch^ris. 102. B. glabra. (L.) 103. H. radiata. (L.) PlCRIS. 104. P. hieraciodes. (L.) Crepis. 105. C. Japonica. (Benth.) Wedelia. 106. W. hispida. (Kunth.) Sonchus. 107. S. oleraceus. (L.) ClCHORlTJS. 108. C. intybus. (L.) 14 200 plants which have become naturalized in n. s. w., Leontodon. 109. L. hirtus. (L.) Tragopogon. 110. T. porrifolius. (L.) Taraxacum. 111. T. dens-leonis. (Desf.) Eubiace^;. Galium. 112. G. aparine. (L.) Sherardia. 113. S. arvensis. (Willd.) CaMPANULACEjE. Lobelia. 114. L. erinus. (L.) PLANTAGINEiE. Plantago 115. P. lanceolata. (Willd.) 116. P. major. (Willd.) Primulace^e. Anagallis. 117. A. arvensis. (L.) Jasmines. Ol;ea . 118. 0. Europaia. (Willd.) AsclepiadacejE. gomphocarpus. 119. 0. fruticosus. (R. Br.) by w. woolls, ph.d.. f.l.s. 201 Apocyneje. VlNCA. 120. V. rosea. (L.) CONVOLVULACEyET Ipoivlea. 121. /. purpurea. (Rot.) CUSCUTA. 122. C.epithymum. (Willd.) SOLANACEiE SOLANUM. 123. S. pseudocapsicum. (L. ) 124. *S\ auriculatum. (Ait.) 125. £. Sodomceum. (L.) Verbasccm. 126. V. blattaria. (L.) Celsia. 127. C Cretica. (L.) NlCANDRA. 128. N. physaloides. (Gaertn.) Lycium. 129. L. Ghinense. (Mill.) Datura. 130. D. Tatula. (L.) Nicotian a. 131. N. glaum. (Grah.) 202 PLANTS WHICH HAVE BECOME NATURALIZED IN N. S. W., SCROPHULARINE^. LlNARIA. 132. L. elatine. (L.) ASPERIFOLIiE. ECHIUM. 133. E. violaceum. (L.) Labiate. Marrubium. 134. M. vulgare. (L.) Stachys. 135. S. arvensis. (L.) Leonites. 136. L. leonurus. (R.Br.) Salvia.. 137. S. verbenacea. (L.) MOLUCELLA. 138. M. hevis. (L.) VERBENACEiE. Lantana. 139. L. camara. (L.) Verbena. 140. V. Bonariensis. (L.) 141. V. venom. (G.& H.) BY W. WOOLLS, PH.D., F.L.S. 203 MONOCOTYLEDONE^E. Iride^. SlSYRINCHIUM. 142. S. BerimTdirmum. (L.) 143. S. micramthum. (Cav.) Trichonema. 144. T. bulbicodium. (U.K.) Sparaxis. 145. S. tricolor. (H.K.) Gladiolus. 146. G. cuspidatus. (H.K.) LlLIACEyE. Zephyranthes. 147. Z. Atamasco. (Herb.) Allium. 148. A. fragrans. (Vent.) Commeline^e. oommelina. 149. C. Africana. (Willd. Graminace^. Stenotaphrum. 150. S. americanum. (Schrank.) Apluda. 151. A. mutica. (L.) 204 PLANTS WHICH HAVE BECOME NATURALIZED IN N. S. W., PHALARIS. 152. P. canariensis. (L.) Anthoxanthum. 153. A. odoratum. (L.) Holcus. 154. H. lanatus. (L.) Avena. 155. A. fatua. (L.) Dactylis. 156. D. ylomerata, (L.) POA. 157. P. annua. (L.) 158. P. glauca. (Sm. ) 159. P. pratensis. (L. ) Briza. 160. B. maxima. (L.) 161. B. minor. (L.) Bromus. 162. B. sterilis. (L). 163. B. mollis. (L.) Ceratochloa. 164. C. unilioides. (L.) BY W. WOOLLS, PH.D., F.L.S. 205 LOLIUM. 165. L. temulentum. (L.) 166. L. perenne. (L.) Hordeujvi. 167. H. nodosum. (L.) 168. H. murinum. (L.) Note. — Psoralea pinnata and Reseda. Inteola are by some regarded as naturalized plants, and Sir J. D. Hooker, places the Peach-tree {Amygdalus a) in the same category. The following species, which also appear in his list, I have omitted, as I have never found them growing in a wild state : — Papciver album. Papaver dubium. EscJi-icholtzia ealifornica. Lathyrus odoratus. Latliyrus latifolius. Lupinus p'tlyphyUus. Delphinium consolidum . 206 THE AUSTRALIAN HYDROMEDUS.E, THE AUSTRALIAN HYDROMEDUS^E. By R. von Lendenfeld, Ph.D. Part L — The Classification of the Hydromedus^e. The Hydvomedusae are here taken in the sense, which Claus (1) attaches to his order Hydroidea. They are characterized by Claus (I.e.) in the following manner : — " Kleine Polypen nnd ramificierte, festsitzende Poly penstock e mit inediisoiden Geschlechtsgemmen oder mit kleinen Medusen als zugehorige Geschlechtsgeneration, sowie kleine mit Randsaum versehene (craspedote) Medusen, ohne polypoide Ammengener- ation." It must be noted, that all Hydroid Zoophytes, " whether they " have Medusoide Geschlechtsgemmen "or" produce generative elements without the aid of medusoid buds, are placed in the order Hydroidea by Claus. The same course will be adopced in this paper. Accordingly the Hydromedusas comprise the Hydroid Zoophytes (Hincks), and the craspedote Medusen (Haeckel), together with the Hydrocorallinse (Moseley.) Although, perhaps only few groups of animals have been the subject of so many papers, as the Hydroruedusse, still our know- ledge, particularly of the Australian representatives of this group, is very limited. Most of the Hydromedusse undergo a change of generation, which is very different in the different Families. The adult animal with sexual products is in many cases a Medusa, and of course it is this stage of the whole cycle of changing generations, which must be considered most in describing, naming and classifying our animals. (1.) C. Claus Grundziige der Zoologie vierte Auflage. Seite, 248. BY DR. K. VON LENDENFELD. 207 The relation between the adult . Medusa and the Hydroid Zoophyte, on which it grows is similar to the relation between an adult Proglottis of a Taenia and the non-sexual head of the tape-worm. It is an accepted custom in every branch of Zoology to classify a series of changing generations, according to that stage in which mature ova and Spermatozoa are found, and it is as expedient to do this here as in any other group of animals. However clear and self-evident this may appear, it has never- theless not been done in the case of our Hydromedusre. Here the non-sexual stages, the colonies of nutritive Zooids, on which the sexual stages bud, are described and classified, whilst the adult Medusa is unknown or ignored. This practice has been followed by most of the authors on Hydroid Zoophytes, although both Haeckel and Claus have shown the fallacy of such a practice. And so the value of papers on this subject, which are written without the consideration of the adult Medusa, is very small. Besides this, in most cases, not even the nutritive Zooids but only their skeletons have been accurately described. Of course this is much easier and more convenient, than to describe the soft Meduspe, which are difficult to obtain- and preserve, and which have no skeleton at all — but it is not scientific. "What would an Entomologist say if the dried skins of the larvae of Cecidomya were used to classify these flies, and they were accord- ingly placed under the annelid worms, instead of placing them according to the structure of the adult Insect in the group of the nemocerous flies. It would appear monstrous, but it is only the same thing that has been done in the case of many Hydroid Zoophites. Besides describing the new forms I have found, the main object of this paper is, to give a list of all the known Australian species, with references. Before entering on the subject it may be worth while to recall to the recollection of the reader a few of the most interesting, points concerning the morphology and physiology of our animals. 208 THE AUSTRALIAN HYDROMEDUS^E, The recent researches of Kleinenberg (1), F. E. Schulze (2), Hertwig (3), Weismann (4), Haraann (5), Jickeli (6), myself (7), and others on the structure of the Hydromedusae, have thrown quite a new light on these animals. With the aid of these authors results and with the help of Haeckel's (8), Monagraph, I hope to be able to extend our knowledge on this subject a little. The great scientific interest which attaches to the study of the Hydromedusa? and the nearly related Siphonophor-a, lies in the Polymorphism of the individuals which belong to one colony. All possible stages in the differentiation of the persons are met with, and it is a thing of particular interest to follow the development of this Polymorphism through its different stages. This Polymorphism is attained in the following manner : — The Hydroids multiply by budding, and all pei-sonsor individuals, with the exception of the free Medusa-stages, which bud from the original Polype, remain in continuity, their stomachs are united by a tube. Now a division of labour takes place among the different persons and consequently they change their shape and structure by natural selection, differing finally very much from each other. (1.) N. Kleinenberg. Hydra, 1S72. (2.) F. E. Schulze. Cordylophora lacustris, 1871- Syncoryne Sarsii, 1873. (3.) 0. und R. Hertwig. Das Nervensystem und die Sinnesorgaue der Medusen, 187S. Der Organismus der Medusen, 187S. (4.) Weismann. Die Entstehung der Geschlechtszellen bei den Hydroiden, 1883. (5.) 0. Hamann. Der Organismus der Hydroidpolypen Jenaische Zeitschrift. Band, XV. Seite. 545. (6.) G. Jickeli. Der Bau der Hydroidpolypen. I., II., Morpholo- gisches Jahrbuch. Band, VIII Seite, 373, 580. (7 ) R. von Lendenfeld. Ueber das Nervensystem der Hydroidpolypen- Zoologischer Anzeiger Nr. 131. Ueber eine eigentniimliche Art der Sprossenbildung bei den Campanulariden. Zoologischer Anzeiger Nr. 130. Ueber Wehrthiere und Nesselzellen Zeitschrift fur wiss. Zool. Band, XXXVIII. Seite, 355. (Translated into English Annales ami Magazine of Natural History. 5 Series. Nr. 71) Eucopella Campanularia Zeit- schrift fur Wissenschaft. Zool. Band, XXXVIII. Seite, 497. (8.) K. Haeckel. Das System der Medusen. Jena, 1879-1880. Die Medusen der Challenger Expedition. Jena, 1S81 (Translated into English. Report of the Zoology of the voyage of the " Challenger.") BY DR. R. VON LENDENFELD. 209 In the simplest case of Protohydra we have a Polype, which multiplies by fission and is propagated by generative elements, produced in the wall of the body. Hydra multiplies by budding and also produces ova and Spermatozoa in the wall of the gastral cavity. Both these Hydroids always remain single and never form colonies : the budding persons are always completely isolated from the parent. The same thing happens in the case of Myriothela. In the stock-forming Hydroida, most of the buds do not attain personal liberty but remain in connection with the primary Polype, their common parent, by tubes through which the nutritive chymus fiows freely. In the simplest case all the Polypes belonging to one colony are alike : Clava is to be compared to a colony of Hydra's. Whilst in Clava and Tabiclava the generative elements are produced by all the Zooids, in other Hydroids the production of generative elements devolves on certain Zoids only, which change their shapes and became Blastostyles ; whilst the other Zooids remain pretty much unchanged in appearance, losing only the I'eproductive faculty. Division of labour causes some persons belonging to the stock — a simple political unity — to become alimentary, and others to attain reproductive functions. To this group belong the Cordylophorinse, Binierinee, Campan- larinse, Sertularinas, and perhaps also the fossil Graptolithes. Also, the Pluinulavidaj are placed in it. The Plumularidaa are characterized by the tranformation of some of the Zooids into Machopolypes. These are persons whose main duty is to defend the stock against outer enemies, and to attack, slay, and bring home, food for the nutritive Zooids. They are the soldiers and fishers of the colony ; often as many as 80% of the Zooids of a colony are thus transformed into soldiers, a state of affairs not even reached by the Continental powers. These Machopolyps, or rather the cups in which they live, were formally called Neuiatothecae or Sarcothecse. 210 THE AUSTRALIAN HYDROMEDUS^, According to Metschnikoff (1) some of these, which possess no thread-cells have also the function of devouring the trophosomes of the colony when they get sick. With great acuteness Metsch- nikoff (I.e.) follows up the similarity between this process and the action of amoeboid wandering cells or white blood corpuscles and festering cells, which perform the same duties in higher animals. By the action of these analogous oi'gaus similar work is performed. These Machapolypes appear in three different forms which are sometimes met with in the same colony. They may possess thread- cells or adhesive cells, similar to those found in the Ctenophorse, or both. I have described the Morphology and Physiology of these Machopolypes elsewhere. (2.) An intermediate stage between the members of this latter group and the Clavidae, is met with in Eudendrium, where there are Blastostyles and Polypes, but Avhereboth may contain ripe ova, and where the Polypes which mature the generative elements afterwards, in many cases lose their tentacles, and so become Blastostyles as it were under the eyes of the observer. I propose to place all Hyclroids mentioned above with the exception of those which produce free Medusae, or which are descended from Hydromedusge which once produced free Zooids, in the first Suborder the Hydropolypinae. The great difficulty in executing this task and classifying the Hydroniedusae accoi'ding to whether their Gonophores are medusoid or not, lies in the great similai-ity between Polypostyles, that is Gonophores derived from a generative Polype direct, and Medusoid Gonophores, that is rudimentary Medusae. I have attempted a classification, comprising all the Hydro- medusa? in the Zoologischer Anzeiger, (3) but I fear, as I pointed (1.) E. Metschnikoff. Ueber die intracellulare Verdaming bei wirbellosen Thieren. Arbeiten aus dem Zool. Inst, der Universitat Wien Band V. (Translated into English, Quarterly Journal of Mik. Science, Nr. 93.) (2.) R. von Lendenfeld. Ueber Wehrthiere und Nesselzellen. Zeitschrift fur wiss. Zool. Band, XXXVIII Seite, 355 (Translated into English Annales and Magazine of Natural History, 5th Series. Nr. 71.) (3.) B. von Lendenfeld. Das System der Hydromedusen. Zoologischer Anzeiger 18S4. BY DR. R. VON LENDENFELD. 211 out in that paper, that many of the statements contained in this first attempt of the kind, are erroneous. Since then a work (1) on the generative elements of the Hydromedusse, has appeared which is equally excellent for the correctness of the observations con- tained therein as for the ingenious conclusions drawn therefrom. Although I did not receive this work until after this paper had been read before the Linnean Society of N. S. Wales, I shall still endeavour to make as much use of it as as possible. The observations contained in this book are given in a table (I.e. p. 214, f.f.), and show, that many of the genera which I had placed in my former (I.e.) paper, among the Hydropolypina?, show in the Gonophores no traces of a medusoid structure. There are a few however, in the Gonophores of which such traces have been discovered by Weismann ; genera which I had placed under the Hydropolypinae. These are Sertularia and Plumularia. Weismann (I.e.), states that two genera, namely Autennularia and Campanularia are peculiar, for the extraordinary difference between the male and female Gonophores. In both these genera the male Gonophores show no trace of the Medusoid structuie, whilst such a structure — several layers of cells outside the gener- tive elements — is met with in the female. Now of course it is quite out of the question to suppose, that the ancestors of these two genera possessed female Medusae, whilst the male Gonophores were always sessil Polypostyles. We must therefore, conclude that both male and female Gonophores descended from free Medusae or from sessile Polypostyles, Weismann considers it probable — any such conclusion of course can only be the more or less probable and never certain — that both descended from free Medusas. Now the male, Dot Medusoid Gonaphores, of these, are quite similar to those of other Hydroids, and so Weismann concludes further, that also these (Aglaophenia Sertularella. Opercularella) have descended from free Mudusae. (1.) A. Weismann. Die Entstehung der Sexnolzellen bei deu Hydro- medusen. Jena, 1883. 212 THE AUSTRALIAN HYDROMEDUS^E, In this manner he brings all but five of those genera which were investigated by him into the group with Medusoid Gono- phores, my Hydrornedusinae. But even these five, with the exception of Hydi-a (I.e. pag. 245 fl\), he finally considers to be Hydromedusae with medusoid buds. These conclusions are mainly based on the observations made by Weismann on the wandering of the generative cells, one of the most important discoveries concerning our animals, which were ever made, statements which also I had occasion to confirm in my paper on Eucopella. The medusae certainly are more recent than the Hyclroid colonies, and there can be no doubt, that the Hydroid colonies must have been propagated sexually before Medusas were formed. It would appear very strange if no such ancestral forms should have come down to us as it is clear that now the free Medusae are in many cases worse than useless and have therefore again become rudi- mentary. The cases of Gonophores which show traces of a Medusoid structure doubtlessly belong partly to the Hydro- rnedusinae as they have really descended from Hydromedusae with free Zooids. On the other hand it is certainly possible that some of these are not rudimentary Medusae but real Polypostyles. It is only a case of greater or smaller probability, and probability always is a subjective feeling. Weismann thinks it probable that these Gonophores are rudimentary Medusae, and his opinion is of great weight if we consider the excellency of his work on the subject, and I dare say he is quite right. I for my own part have not been convinced by his publication, and consider it as probable that Gonophores, which are not rudimentary Medusae, do exist. Whether all the forms, which according to my idea, have other Gonophores, and therefore ai'e placed among the Hydropolypinae really belong there, is another question. In doubtful cases I decided according to the position of the Gonophore for the reasons given in my former paper (Zoologischer Anzeiger) on this subject. The Hydroid colonies are often overgrown by tufts of Diatoms and other Protista, and a Medusa produced near the base of the BY DR. R. VON LENDENFELD. 213 colony would in consequence not be able to swim away whilst the small embryo escaping the Gonongium could easily penetrate the marine undergrowth, which, of course, in this case, is of advantage to the colony, hiding and sheltering the Gonophore. I have, therefore, in doubtful cases, placed those Hydro- medusinae, which have Gbnophores at the base of the colony under the Hydropolypinae, those on the other hand, which bear exposed Gonophores under the Hydromedusinae. The first suboi'der of the Hydromedusse, the Hydropolypinae, comprises accordingly Hydi'a, the Clavidae, Eudench'idae, Cordy- lophorinae, Bimei-ina?, Campanularinae, Sertularinae, the Plumu- laridse, and Dicorynidae. I have also placed the Graptolithidae under this heading. We meet with cpiite a different kind of Polymorphisne in another series of Hydrornedusse. Here Medusas are formed, that is Hydroid persons, which lead a free life and are provided with an apparatus for free locomotion. This apparatus is in most cases a bell-shaped Umbrella, an extremely clumsy and unsuitable propelling organ. Only very few Medusae are destitute of an Umbrella and crawl on their mai-ginal tentacles like Clavatella (Eleutheria.) These Medusae, which had originally the function of distributing the species like the winged Imagines of Insects, with which they are to be compared, are small when born and often grow to a large size afterwards. In such cases the nourishment assimilated by the Medusa greatly exceeds that, which the Polyp colony needs. Such Hydromedusae however (Zygodoctyla) are rare. In most cases they remain small, losing more and more the function of taking up noui-ishment which in such cases devolves on the Polyp colonies. Finally Medusa? are produced which only live a short time (Globiceps), and which already bear ripe sexual products at the time of their liberation. The stomach of such Medusae may even be obliterated (Eucopella) and an organism is produced, which like the Ephemera is in fact only an apparatus for carrying the sexual product to a greater distance like the Hectokotylus. 214 THE AUSTRALIAN HYDROMEDUS-E, These rudimentary Medusae, produced, of course, in the ordinary course of natural selection, show that it is in many cases advantageous for the species not to have free swimming stages. In consequence of this the Medusae may even become more rudimentary, and finally remain attached to the Hydroid colony, where they mature the sexual products within them (Tabularia.) When ijhey have once become so far rudimentary, their parts, particularly the locomotive organ, the Umbrella will be obliterated, unless it is utilised for some other purpose (Weismann, Dohrn), and we shall finally have a Medusoid Gonophor before us. According to Weismann all Gonophores are rudimentary Medusae as stated above. I, however, do not wholly agree with Weismann on this point, although I gladly admit that this is quite possible. I place all Hydroid colonies which produce Medusas, and also those which possess Gonophores of a doubtless medusoid origin in this group, which I designate as the second Suborder of the Hydromedusae, the Hydromedusinae. I accordingly place the Anthomedusidae (Anthomedusse Haeckel), the Tubularidae (com- prising Coryne, Myriothela, Stylactis, Tubularia, Pennaria and related genera), the Leptomedusidae (Leptomedusae Haeckel), and those Campanularidae which possess decidedly medusoid Gono- phores as Gonothyrea and Halecium in this suborder. In the first of these families, the Medusae bud on all the Zoids and become free, in the second they also bud on all Polypes of the stock, but are more or less rudimentary. In the third and fourth family the Medusae bud on differentiated Polypes, Blastostyls becoming free in the one and rudimentary in the other. Some Hydroid colonies producing Medusae, which belong to Haeckel's Margelidae, are so different from the others that I place them in accordance with Glaus in a separate family the Hydractinidae, which evidently connects the calcareous Hydro- corollinae with the chitinous Hydromedusinae. The Hydrocorallinae themselves, which I reckon as the third suborder, also produce Medusae, or at least some of them do, but the calcareous skeleton seems to me to be so important a characteristic, because it points to fundamental chemical differences BY DR. R. VON LEXDENFELD. 215 in the Protoplasme, that I separate them in accordance with Claus from the other Hydromedusee. The process described above, by which the Medusae became more and more rudimentary, was apparently advantageous only for one series of Hydromedusae, whilst in another series we find the Hydroid colony becoming more and more rudimentary inasmuch as the nourishment is more and more assimilated by the Medusa stage and less by the Polypes. This process which is indicated in Zygodactyla may go so far that the Polype stages are finally done away with altogether, and a Medusa is produced direct from the ovum without the inter- mediate stage of a Polype. In this manner the change of generation is done away with altogether and we have Medusa? before us, which, although probably descended from Hydroid ancestors, show no trace of such a descendance, and now only the comparative anatomy of these forms proves that they belong to our Hydroniedusae. Such Medusae are very numerous. Clatcs combines all these forms in his suborder Trachomedusse, which corresponds with our fourth suborder Trachoniedusinse. The Trachotnedusinse comprise Haeckel's Trachomedusae and Narkomedusee, which correspond to our families Trachomedusidae and Narkomedusidae. It appears to me that the total neglect of those Hydromedusai, which do not produce free Medusae, in Haeckel's System der Medusen is not true to nature. If Haeckel considers the Lucernaridae as part of the Acraspaedaa which they doubtlessly are, one would also expect that he would include the Hydroid Polypes in his Craspedotae. And I think I shall follow out Haeckel's ideas better by placing them there than by separating them from those Hydromedusae which produce free zoids. The difference between Craspedotae and Acraspedae is so great that it seems advantageous to separate these two groups entirely. In this point I agree with Claus. The great similarity between the two is only analogy and not homology. At all events the Hydroid Zoophytes are much more nearly related to the Ciaspedote Medusae than the latter to the Acraspedae. 15 216 THE AUSTRALIAN HYDROMEDUSSE, The Polypomedusee form in my classification the second classis of the subtype Cnidaria (1), (Claus) of the Coelenterata, and comprise all polypiform and Medusiform animals. I have selected this name for the Hydromedusse of Claus (2), and given the reasons for doing so in my preliminary report (3). Since then I have received Claus's Lehrbuch of Zoology (4), and I find that Claus also has adopted in the latter publication this term, which I had found independently to be the most expressive. The Polypomedusae as a classis are devided into the three ordines Hydromedusa? (Hydroidea Claus, Hydromedusse Weis- ma?in), Syphonophora and Scyphomedusal (Ray Lankaster, Acras- paedse Gegenbaur, Haeckel.) Our Ordo Hydromedusse is, as mentioned above, to be divided into four suborders. The relative value of these classificatory terms is elucidated in the following table : — Type Coelenterata. 1. Subtype Spongise. 2. Subtype Cuidaria. Subtype Cuidaria. 1. Classis Anthozoa. 2. Classis Polypomedusse. 3. Classis Ctenophorse. Classis Polypomedusae. A , n ( 1. Ordo Hydromedusa?. Aphacellse < J ( 2. Ordo Syphonophora. Phacellotse 3. Ordo Scyphornedusse. (].) Marshall has objected in a recent publication (Die Ontogenie von Reniera filigrana, Zeitschrift fiir wiss. Zool. Band XXXVII.) to this term on the ground that it "den Begriff nicht deckt " (I.e. Seite 243 Anmer- kung), I don't see what advantage would be gained in altering Claus's generally adopted term in this case. (2.) C. Claus. Grundziige der Zoologie, 4te Auflage, Seite 243. (3.) JR. v. Lendenfeld. Das System der Hydromedusen. Zoologischer Anzeiger, Band VI., 18S4. (4.) C. Claus. Lehrbuch der Zoologie 1883, Seite 306. by dr. r. von lendenfeld. 217 Ordo Hydromedus^:. 1. Subordo Hydropolypinse. 2. ,, Hydromedusinse. 3. „ Hydrocorallinse. 4. ,, Trachoniedusinse. If we now classify the Hydromedusse according to the principles set forth above we shall arrive at the following classificatory system : — Schemas are attached to the diagnoses. The italics represent stages which do not take up nourishment, the stages given in ordinary print represent such which do. The schema's also show the way in which the budding process alternates with the sexual propagation. As the change of generation is caused by this alternation on the one hand and influenced mainly by the phase in which nourishment is taken up, these schema's will elucidate the differences which are met with among the Hydromedusse in this respect. The most important genera are mentioned. Genera which are imperfectly known have been omitted. 218 THE AUSTRALIAN HYDROMEDUS.E, ORDO, HYDROMEDUSX Cams, 1863. HYDROPHORAE. Huxley, 1856. HYDROIDEA. Agassiz, 1862. HYDROID^. Claus, 1876. THE POLYPCOLONIES. HYDROID ZOOPHITES. Hinks, 1868. (Old term.) THE MEDUSAE. CRASPEDOT^E. Gegenbaur, 1856. CYCLONEUELE. Eiiner, 1878. APHACELL^E. Haeckel, 1878. CRASPEDOT^E. Haeckel, 1879. (1.) POLYPES WITHOUT GASTRAL FILAMENTS OFTEN IN COLO- NIES, SOMETIMES WITH GREATLY TRANSFORMED GENERA- TIVE OR DEFENSIVE PERSONS, AND CYCLONEUROUS MEDUSAE, WITHOUT GASTRAL FILAMENTS. I.-SUBORDO HYDROPOLYPIN^E. Von Lendenfeld, 1884. HYDROMEDUS^E GENERALLY FORMING COLONIES OF ALI- MENTARY AND GENERATIVE PERSONS. THE TWOFUNCTIONS MAY DEVOLVE ON ALL PERSONS ALIKE, OR BE EXECUTED BY DIFFERENT ZOOIDS. RARELY SOLITARY. NOT PRODUCING MEDUSA. THE BLASTOSTYLS OF THE HYDRO POLYPIN^E ARE TRANSFORMED POLYPES AND NOT RUDIMENTARY MEDUSAE. ( 1 . ) Other synonyms in the works referred to. BY DR. R, VON LENDENFELD. 219 I. FAMILY HYDKID^E. Huxley, 1856. Multiplying by budding or fission, and by sexual cells produced in every Polype (1) Solitary. -SCHEMA. Polype Ovum Polype I Ovum. Protohydra. Greff. Hydra. Linne. Etc. 2. FAMILY CLAYID^E. Yon Lendenfeld, 1884. non Allman ! Forming colonies, all persons alike and all maturing (2) sexual cells on hollow tentacular pi'ocesses. SCHEMA : Ovum I Polype I Hydrorhiza I First Polype I Ovum. (1.) In this and in other similar cases it is very likely, and has indeed been observed, that although the Polypes which produce ova are similar to others which may not appear adult ; budding and sexual propagation are not carried on by the same individual at the same period. It appears likely, that here, as in the Infusoria, periods of sexually multiplying and budding generations alternate, and so a division of labour in time exists, which may lead to a division of labour in space, if the budding persons remain attached to one another. (2.) " Maturing " in this and the following definitions, because the generative elements in many cases are produced elsewhere, and wander into the place, where they finally reach maturity at a comparatively late period. 220 THE AUSTRALIAN HYDROMEDUS^E, 1. SUB-FAMILY CLAVINxE, With scattered filiforme tentacles. Clava. Gmelin. Tubiclava. Allman. Rhyzogeton. Agassiz. 2. SUB-FAMILY CORYNIN.E. Withjscattered capitate tentacles. Coryne. Gartner. Actinogonium. Allman. Wrightia. Allman. Stylactis. Allman. 3. FAMILY MYRIOTHELID^E. Allman, 1872. Solitary with scattered capitate tentacles. Some of the tentacles are transformed and bear the sexual products. SCHEMA. Polype Ovum I Polype. Myriothela. Sars. 4. FAMILY EUDENDRIM:. Allman, 1872. Forming colonies, all Polypes may mature sexual product whereby they are often changed into Polypostyles without mouth or tentacles. SCHEMA. Ovum Ovum I I Polype Polypostyl Hydrorhiza I First Polype I Ovum. Endendriam. Allman. BY DR. R. VON LENDENFELD. 221 5. FAMILY BLASTOPOLYPID^E. Von Lendenfeld, 1884. Forming colonies with differentiated Alimentary and Generative Zooids. The latter are Polypostyles and mature the sexual products. The Alimentary Zooids do not take part in the sexual i (^production. _SCHEMA. Ovum I Polype Polypostyl Hydrohiza I First Polype I Ovum. I. SUB-FAMILY. CORDYLOPHORIN^. Alimentary Zooids of the Colony, with scattered filiform, tentacles not protected by a chitinous cup. Cordylophora. Allman. Merona. Norman. II. SUB-FAMILY. BIMERUSLE. Alimentary Zooids with one verticil of filiform tentacles, not protected by a chitinous cup. Heterocordyle. Allman. Pachycordyle. Weismann. Garveia. St. Wright. Bimeria. St. Wright. Coinistes. St. Wright. Etc. III. SUB-FAMILY. CAMPAXULARIN^E. Alimentary Zooids, with one verticil of filiform tentacles in chitinous cups which are connected with the Hydrorhiza by more or less developed stalks, and never adnate to the stem. Campanularia. Lamarck. Opercularella. Hincks. Calycella. Hincks. Etc. 222 THE AUSTRALIAN HYDROMEDUS.E, IV. SUB-FAMILY. SERTULARIN^. SERTULARID/E. Hincks. Alimentary Zooicls, invested by chitinous cups, which are more or less adnate to the stem, and never possess separate Hydrocauli. Lineolaria. Hincks. Sertularia. Linne. Diphasia. Agassiz. Sertularella. Gray. Pasythea. Lamouroux. Idia. Laumouroux. Thuiai'ia Fleming. Hydrallmania. Hincks. Triplograptus. Richter. Corynoides. Nicholson. Dendrograptus. Hall. Callograptus. Hall. Dictyonema. Hall. Ptilograptus. Hall. Thomnograptus. Hall. Buthograptus. Hall. Tnocaulis. Hall. G. FAMILY. GRAPTHOLITHID^:. Possessing a chitinous Endo- and Exo-skeletori. The former rod-shaped. Colonies free swimming, probably extinct. From the Cambrian to the lower Devonian. I. GROUP. GRAPTOLIDEA. Lapworth. Hydrosom developed from a Sicula, every canal containing Coenosarc, bears only one row of cells. Axis (Virgula) on the dorsal side in a furrow of the inner lamina. A. MONOPRIONID/E. Hydrotheca? in oue row opposite the axis. BY DR. R. VON LENDENFELD. *2 2 3 1. SUB-FAMILY. MONOGROPTINJE. MONOGROPTIDvE. Lapworth. Developed one-sided ; pointed ends of the Sicula pointing upwards, united with the dorsal margin of the proximal end of a single or composite Hydrosome. Monograptus. Geinitz. Rostrites. Barrande. Cryptogi'aptus. Carruthers. Azygograptus. Nicholson. Dimorphograptus. Lapworth. 2. SUB-FAMILY. LEPTOGRAPTIN^E. LEPTOGRAPTID.^. Lapworth. Hydrosom bilateral, with irregular branches. Cells apart, just touching. Sicula persistent in the axilar. The broad part forming the proximal end of the Hydrosome. Leptograptus. Lapworth. Amphigraptus. Lapworth. Pleurograptus. Nicholson. Nemograptus. Emmons. Coenograptus. Hall. 3. SUB-FAMILY. DICHOGRAPTESLE. DICHOGRAPTID^E. Lapworth. Bilateral. Branches of regular cells, very dense, rectangular Sicula persistent. Its point at the proximal end of the Hydrosome. Didymograptus. McCoy. Trichograptus. Nicholson. Tetrograptus. Salter. Goniograptus. McCoy. Schizograptus. Nicholson. Temnograptus. Nicholson. Ctenograptus. Nicholson. Dichograptus. Saltei*. Lagonograptus. Hall. Clonograptus. Hall. Clematograptus. Hopkins. Cladograpsus. McCoy 224 THE AUSTRALIAN HYDROMEDUS.E, 4. SUB-FAMILY. DICRANOGRAPTIN/E. DICRANOGRAPTID/E. Lapworth. Hydrosom consists of two originally dorsally united axes. Cells overlapping. Exterior part indented. Broad end of the Sicula on the proximal end of the Hydrosoina. Dicellograptus. Hopkins. Dicranogi'aptus. Hall. B. DIPRIONIDiE. Cells in two rows, axis central. 5. SUB-FAMILY. DIPLOGRAPTIN^. DIPLOGRAPTID.E. Lapworth. Hydrosom consists of two branches dorsally joined. Sicula imbedded. The broad part forming the proximal end of the Hydrosom. Climacograptus. Hall. Diplograptus. McCoy. Glyptograptus. Lapworth. Petalograptus. Suess. Cephalograptus. Hopkins. 6. SUB-FAMILY. PHYLLOGRAPTIN^E. PHYLLOGRAPTID^E. Lapworth. Hydrosom consists of four biserial axes, which coalesce with their dorsal sides. Sicula imbedded. The broader ends close to the pi'oximal terminations of the Hydrosoms. Phyllograptus. Hall. II. GROUP. RETIOLOIDzE. Lapworth. No Sicula. The Coeaosark of the common canal developes a double row of cells. Epidermis supported by chitnious fibers. 7. SUB-FAMILY. GLASSOGRAPTIN/E. GLASSOGRAPTIDvE. Lapworth. Both axes united in the middle of the body. Retiograptus. Hall. Sasiograptus. Lapworth. BY DR. E. VON LENDENFELD. 225 8. SUB-FAMILY. GLADIOGRAPTI^E. GLADIOGRAPTID^E. Lapworth. Both axes separate. Perfect exoskeleton of chitinous fibres. Clathrograptus. Lapworth. Trigonograptus. Nicholson. Retiolithes. Barrande. 7. FAMILY PLUMULARID^E. Hincks, 1868. Forming a colony. Alimentary and Generative Zooids, and Machopolyps. Alimentary Zooids with one verticil of filiform Tentacles. Ovum Blastostyl Polyp Machopholyp Hydroriza. I First Polyp I Ovum. Ophiodes. Hincks. Plumularia. McCrady. Antennularia. Lamarck. Aglaophemia. McCrady. Halicornaria. Busk. Halicornopsis. Bale. Sciarella. Allman. Acanthella. Allman. Schizatricha. Allman. Polyplumaria. Sars. Heteroplana. Allman. Acanthochladium. Allman. Lithocarpus. Kirchenpauer. Kirchenpaueria. JickelL Streptocaulus. Allman. Diplochilus. Allman. Cladocarpus. Allman. Azigo plana. Allman. Etc. 226 THE AUSTRALIAN HYDROMEDUS^, 8. FAMILY DICORYNID^E. Allman. Generative Zooids free swimming Polypes with two tentacles and without a mouth, carrying two ova each. These Zooids bud only on Polypostyles, and never on the Alimentary Zooids which have one verticil of filiforine tentacles. SCHEMA. Ovum Free Polypoid I Polyp Poly-postyl Hydrorldza I First Polyp I Ovum. Dicoryne. Allman. II. SUBORDER HYDROMEDUSIN^E. Von Lendenfeld, 1884. COLONIES OF POLYMORPHIC ZOOIDS. THE ALIMENTARY ZOOIDS RETAIN THE SHAPE OF POLYPES, WHILST THOSE IN WHICH THE SEXUAL PRODUCTS REACH MATURITY ARE MEDUSAE, WHICH MAY BECOME FREE OR REMAIN ATTACHED TO THE COLONY AND BECOME RUDIMENTARY. 9. FAMILY ANTHOMEDUSIDA^E. Von Lendenfeld, 1884. Anthornedusa?. Haeckel, without the Cytaeidae of Haeckel. Medusae become free, without Otoliths, with Ocelli at the base of the tentacles. Gonads in the outer or oral wall of the gastral cavity. Mostly four Radial Canals. The Polype colonies on which these Medusae bud, contain alimentary Zooids, which are not invested by chitinous cups. The Medusae bud mostly on the ordinary alimentary Polypes, exceptionally they are also born on peduncles and bud direct from the Hydrorhiza. A division of labour between alimentary Polypes and Polypes, which produce Medusae, Polypostyles does not occur. BY DR. R. VON LENDENFELD. 227 SCHEMA. . Ovum I Medusa I Polyp - I Hydrorhiza I First Polyp I Ovum. or : Ovum Medusa Ovum Medusa Polyp rr I Hydrorhiza First Polyp I Ovum. or : Ovum Polyp Medusa V Hydroriza First Polyp _ I Ovum. 228 THE AUSTRALIAN HYDROMEDUSyE, I. SUB-FAMILY. CODONIN^. CODONLILE. Haeckel. Mouth simple, with flaps or barbels. Gonade simple tube shaped, not divided radially, with four simple Radial Canals and unbranched tentacles. Alimentary Zooids, with tentacles, which are scattered, or in two verticils. Codonium. Haeckel. Sarsia. Lesson. Syndictyon. A. Agassiz. Ectopleura. L. Agassiz. Dipurena. MacCrady. Bathycodon. Haeckel. Dicodonium. Haeckel. Dinema Van. Beneden. Steenstrupia. Forbes. Euphysa. Forbes. Hybocodon. L. Agassiz. Ampbicodon. Haeckel. Amalthaea. O. Schmidt. Globiceps. Ayres. Gymnocoxyne. Hincks ? Vorticlava. Alder. Acharadria Strethill. Wright. Dendroclava. Weismann. II. SUB-FAMILY. TIARIN^E. TIARID^E. Haeckel- Anthomedusidse with four broad Moutharms, with four or four pair of gonads, four simple Radial Canals and unbranched tentacles. The alimentary Zooids of the Polypecolonies with scattered capitate tentacles. Protiara. Haeckel. Moderia. Forbes. Corynites. McCrady. Amphinema. Haeckel. Codonorchis, Haeckel. BY. DR. R. VON LENDENPELD. 229 Stomodoca. L. Agassiz. Panthaea. Lesson. Conis. Brandt. Tiara. Lesson. Tunis. Lesson. Catablema. - Haeckel. Turritopsis. McCrady. Callitiara. Haeckel Corydendrium Van. Beneden 1 III. SUB-FAMILY. MARGELIN^E. Margelidse. Haeckel, with the exceptian of Haeckel's Genera Cytaeis, Cubogaster, Dysinorphosa, Cytasandra.) Anthoniedusae, with simple or branched moutharms. Gonade divided into four or eight marginal flaps. The Medusae bud on Colonies of Polypes, which contain alimentary Zooids, with a verticil of filiform tentacles. Lizusa. Haeckel. Lizzia. Forbes. Lizzella. Haeckel. Thamnitis Haeckel. Thamnostylus. Haeckel. Thamnostoma. Haeckel. Limnorea. Peron. Margelis. Steenstrup. Hippocrene. Mertens. Nemopsis. L. Agassiz 1 Margelium. Haeckel. Rathkea. Brandt. IV. SUB-FAMILY. CLADONEMIN^E. CLADONEMID^E. Gegenbaur. Anthoniedusae, with branched tentacles, with 4 — 8 simple or branched Radial Canals, and four or four pair of gastral Gonads. The Medusae bud on Polypecolonies which contain alimentary Zooids, with scattered capitate tentacles. Pteronema. Haeckel. Zanclea. Gegenbaur. 230 THE AUSTRALIAN HYDROHEDUS.E, Gemmaria. McCrady. Eleutheria. Quatrefages. Ctenavia. Haeckel. Cladonema. Diyardin. Dendronema. Haeckel. Heterostephanus. Allman ? 10. FAMILY TUBULARLD^E. Von Lendenfeld, 1884. The Medusas in tins family become more or less rudimentary, and remain attacked to the Polypes. All Zooids are alike and all bear Medusae. SCHEMA. Ovum Medusoid bud I Polyp I Hydrorhiza I First Polyp I Ovum I. SUB-FAMILY. PENNARIN^E. The Polypes possess a distal set of capitate and a proximal set of filiform tentacles. Pennaria. Goldfuss. Halocordyle. Allman. Monocaulus Sars 1 II. SUB-FAMILY. TUBULARIN.E. The Polypes possess two verticils of filiform tentacles. Tubularia. Allman. III. SUB-FAMILY. ATRACTYLIN.E. The Polypes possess a single verticil of filiform tentacles. The medusoid buds are produced on the Uydrocaulus. Atractvlis. Hincks. BY DR. R. VON LENDENFELD. 231 11. FAMILY LEPTOMEDUSID^E. Von Lendenfeld, 1884. LEPTOMEDUS.E. Haeckel. Medusea with Ocelli or Ectodermal Otolithes and Gonads, developed in the walls of the Radial Canals. Medusae always budding on transformed Polypes, Polypostyls and never on the alimentary Zooids. Alimentary Zooids and Polypostyles invested by a chitinous Perisarc. SCHEMA : Ovum I Medusa Polyp Polypostyl V Hydrohiza I First Polyp Ovum. I. SUB-FAMILY THAUMANTINA. THAUMUANT1D.E. Gegenbaur. Leptomedusa? without marginal vesicles, simple Ptadial Canals. Tetranema. Haeckel. Dissonema. Haeckel. Octonema. Haeckel. Thaumtias. Eschscholtz. Staurostoma. Haeckel. Laodice. Lesson. Melicertella. Haeckel. Melicertissa. Haeckel. Melicertum. A. Agassiz. Melicertidium. Haeckel. Orchistoma. Haeckel. 16 232 THE AUSTRALIAN HYDROMEDUSCE, II. SUB-FAMILY. CANNOTIN,E. AKNOTIDiE. Haeckel. Leptonieduspe, without marginal vesicles, with branched Radial Canals. Staurodiscus. Haeckel. G-aninerna. A. Agassiz. Ptychogena. A. Agassiz. IStauropkora. Brandt. Polyorchis. A. Agassiz. Cannota. Haeckel. Discannota. Haeckel. Berenice. Peron et Leseur. Dipleurosoma. A. Boeck. Dicronocanna. Haeckel. Toxorchis. Haeckel. Veletta. Haeckel. Willia. Forbes. Proboscidactyla. Brandt. Cladocanna. Haeckel. III. SUB-FAMILY. EUCOPIX.E. EUCOPID^E. Gegenbaur. Leptomedusse, with marginal vesicles and four simple unbranched radial canals. Eucopium. Haeckel. Saphenella. Haeckel. Eucope. Gegenbaur. Obelia. Peron et Leseur. Tiaropsis. L. Agassiz. Euchilota. McCrady. Phialium. Haeckel. Pbialis. Haeckel. Mitrocomium. Haeckel. Epeuthesis. McCrady. Mitrocomella. Haeckel. Phialidium. Lemkart. BY DR. R. VON LENDENFELD. 233 Mitroconia. Haeckel. Eutiminiu. Haeckel. Eutima. McCrady. Saphenia. Eschsckoltz. Eutirueta. Haeckel. Eutimalplaes. Haeckel. Octorckidium. Haeckel. Octorckis. Haeckel. Octorchandra. Haeckel. Irenium. Haeckel. Irene. Escksckoltz. Tima. Escksckoltz. IV. SUB-FAMILY. EUCOPELLIN.E. Von Lendenfeld. Medusa without stomach, highly developed organs of sense, no tentacles, eight marginal vesicles. Four radial canals, which send branches into the Gonads. Alimentary Zooid, with 32 tentacles and a Perisarc. Blastostyl consisting of four radial tubes, between which the Medusae bud. Ova formed as in the Conipanularinse in the Hydrorhiza. SCHEMA : Ovum I Medusa I Poly Blastostyl V Hydrorhiza I First Polyp I Ovum, Eucopella. Von Lendenfeld. 234 THE AUSTRALIAN HYDROMEDUSiE, V. SUB-FAMILY AEQUORIN^E. Aequoridee. Eschscholtz. "With marginal vesicles and numerous (at least 8), often branched Radial Canals. Octacanna. Haeckel. Zygocanna. Haeckel. Zygocannota. Haeckel. Zygocannula. Haeckel. Halopsis. A. Agassiz. Aequorea. Peron et Leseur. Rhegmatodes A. Agassiz. Stomobrachium. Brandt. Staurobrachium . Haeckel. Mesonema. Eschscholtz, Polycanna. Haeckel. 12. FAMILY CAMPANULINID^E. Von Lendenfeld, 1884. Colonies of Polypes which ate differentiated into alimentary Zooids with one verticil of filiform tentacles and generative Polypes, Polypostyles without mouth or tentacles. Both kinds of Zooids are invested by chitinous capsules. The Polypostyles only produce by budding sexual Zooids, which are rudimentary Medusae and never become free. SCHEMA : Ovum I medusoid btid I Polype Polypostyl Hydrorhlza I First Polyp. I Ovum. Gonothyrea. Allman. Halecium. Oken. (According to "Weismann all the genera placed under the heading Campanularidge, should be placed here.) BY DR. R. VON LENDENFELD. 235 13. FAMILY HYDRA.CTINID.E. Von Lendenfeld, 1884. Hydractinidae. Claus (1). Polypecolonies with free or rudimentary Medusae. The free Medusae belong to Haeckels Sub-family Cytaeidae, and possess Ocelli at the base of the tentacles, and no Otolithes. The tentacles are scattered and equally distributed. With simple Moutharms. The Polype colonies consist of a dense mass of entwined Hydro- rhizse from which the Hydrocauli, simple or slightly branched grow forth. The alimentary Zooids possess one verticil of filiform tentacles. The Medusae bud from the Hydrorhiza, or on mouth- less Polyps, Polypostyles, rarely on the alimentary Polypes. Besides the alimentary and Generative Zooids we meet with defensive Spiral Zooids. (P. Wright.) I. SUB-FAMILY CYT^EUSLE. Cytaeidse. Haeckel. Producing free Medusae, which bud from the Hydrorhiza. SCHEMA : Ovum Medusa Polype Spiralzoid entwined Hydrorhiza, basal plate First Polype Ovum. Cyteeis. Eschscholtz. Cubogaster. Haeckel. Dysrnorphosa. Philippi. Cyteandra. Haeckel. Corynopsis. Allman. II. SUB-FAMILY HYDRACTININ^. Medusae bud on Polypostyls, remain sessile and become rudi- mentary (or immersed in the basal plate V) 236 THE AUSTRALIAN HYDROMKDUB^, SCHEMA : Ovum I . medusoid bud I Spiralzooid Polype Polypostyl entwined Hydrorhiza, basal plate I First Polype I Ovum Hydractinia. Van Bemeden. Coppinia, Hincks 1 III. SUBORDER HYDROCORALLIJSLE. Moseley. ALIMENTARY ZOOIDS WITH FEW VERTICILLATE, CAPITATE TENTACLES. HYDRORHIZA FORMING A DENSE CALCAREOUS SKELETON WHICH ALSO INVESTS THE POLYPES. GROUPS OF MACHAPOLYPES, IN THE FORM OF TENTACULAR ZOOIDS, SURROUND THE ALIMENTARY POLYPES. Ultimately generative Zooids are probably Medusae SCHEMA (?) : Ovum I Medusa I Machopohjp Polype Hydrorihiza I First Polype I Ovum. BY DR. R. VON LENDEXFELD. 237 14. FAMILY. STROMATOPOMD^E. Murie and Nicholson. Possessing undulating laminae in the skeleton. Stromatopora. Goldfuss. Stylodictyon. Murie and Nicholson. Clathrodictyon. Murie and Nicholson. Pachystroma. Murie and Nicholson. Dictyostroma. Murie and Nicholson. Ellipsactinia. Steinmann. Cannopora. Murie and Nicholson. Stromatocerium. Murie and Nicholson. Labechia. Lansdale. Etc. 15. FAMILY. MILLIPORID.E. Moseley. Alimentary Zooids, with from 4 to 6 tentacles. Polypary with many conic protuberances divided by Tabula?. Coeneuchym with reticulating canals. Millepora. Linne. Pliabothrus. Pourtales. Axopora. Edwards. Porosphaera, Steinmann. Cylindrohyphasma. Steinmann. Etc. 16. FAMILY. STYLASTERIDJE. Gray. Alimentary Zooids with from 4 to 12 tentacles. Massive Hydrosom containing tubes which possess pseudosepta formed by the regular position of the tentacular Zooids. Cryptohelia. E. H. Stylaster. Gray. Allopora. Ehrenberg. Polypora. Eudobelia. E. H. Distichopora. Verill. Lepidopora. Pourtales. Errina. Gray. Pentalophora. Kent. Etc. 238 THE AUSTRALIAN HYDROMEDUS.E, IV. SUBOEDER TRACHOMEDUS1NJE. Von Lendenfeld, 1884. TRACHOMEDUS^ CLAUS. HYDROMEDUS^ WHICH ARE MEDUSiE, AND ARE PROPA- GATED SEXUALLY WITHOUT A CHANGE OF GENERATION AND WITHOUT FORMING POLYPOID ZOOIDS. MEDUS-2E WTITH ENTODERM AL ACUSTIC CLUBS. SCHEMA : Ovum I Medusa I Ovum or : Ovum ! Medusa Ovum Medusa I Ovum. 17. FAMILY TRACHOMEDUSID^E. Von Lendenfeld, 1884. Trachomedusae. Haeckel. The Gonads are developed in the walls of the Radial Canals. 1. SUB- FAMILY PETASNLE. Petasidse. Haeckel. With 4 Radial Canals, with long tube shaped stomach. Acustic clubs free or in vesicles on the margin of the Umbrella. Petasus. Haeckel. Dipetasus. Haeckel. Petasata. Haeckel. Petachnum. Haeckel. Aglauropsis. F. Miiller. Gossea. L. Agassiz. Olindias. F. Miiller. BY DR. R. VON LENDENFELD. 239 II. SUB-FAMILY. TRACHINEMINiE. TRACHINEMID^E. Gegenbaur. With 8 Radial Canals, with long tube-shaped stomach. Trachyneraa. Gegenbaur. Marmanema, Haeckel. Rhopalonema. Gegenbaur. Pectillis. Haeckel. Pectis. Haeckel. Pectanthis. Haeckel. III. SUB-FAMILY. AGLAURIN^. AGLAURIDJE. L. Agassiz. With 8 Radial Canals and with a pedicle to the stomach. Aglantha. Haeckel. Aglaura. Peron et Lesseur. Stauraglaura. Haeckel. Persa. McCrady. IV. SUB-FAMILY. GERYONIN.2E. GERYONID^. Haeckel. Four or 6 radial tubes, leaf-shaped gonads. Long stomach pedicle, 8 or 12 marginal peronise, and as many acustic vesicles. Liriantha. Haeckel. Liriope. Lesson. Glossoconus Haeckel. Glossocodon. Haeckel. Geryones. Haeckel. Geryonia. P6ron et Leseur. Carmaris. Haeckel. Carmarina. Haeckel. 18. FAMILY. NARKOMEDUSID^E. Von Lendenf eld, 1884. NARKOMEDUS^. Haeckel. Trachomedusse, with gastral gonads. 240 THE AUSTRALIAN HYDROS! EDUSiE, I. SUB- FAMILY. CUNANTHIN/E. CUNANTHID.E. Haeckel. With broad pouch-shaped Radial Canals, with otoporpa. Cunantha. Haeckel. Cunarcha. Haeckel. Cunoctantha. Haeckel. Cunoctona. Haeckel. Cuuina. Eschscholtz. Cunissa. Haeckel. II. SUB-FAMILY. PEGANTHIN^, PEGANTHID^E. Haeckel. Without Radial Canals and without gastral pouches in the sub- umbrella. With otoporpa. Polycolpa. Haeckel. Polyxenia, Eschscholtz. Pegasia. Peron et Leseur. Pegantha. Haeckel. III. SUB-FAMILY. AGEININ-ffi. AEGINIDiE. Gegenbaur. Circular canal in communication with the gastral cavity by double peranial tubes. With gastral pouches without otoporpa. Aegina. Eschscholtz. Aeginella. Haeckel. Aegineta. Gegenbaur. Aeginopsis. Brandt. Aeginura. Haeckel. Aeginodiscus. Haeckel. Aeginodorus. Haeckel. Aeginorhodus. Haeckel. IV. SUB-FAMILY. SOLAMARIN^I. SALMARID^]. Haeckel. Without circular canal and without otoporpa, with or without Radial Canals. Solmissus. Haeckel. BY DR. E. VON LENDENFELD. 241 Solmundus. Haeckel. Solmundella. Haeckel. Solmoneta. Haeckel. Solmaris. Haeckel. In this list, of course, by no means all known genera are mentioned, but I have endeavoured not to omit any of the more recently established ones. The older genera, for instance, of Lomouroux and Lamai'ck, and those recent ones, which appear too doubtful, have not been included. This classification will, like all its predecessors, doubtlessly be full of errors, but I think the leading idea of it is the correct one, although the application of it in detail has in many cases very likely been a wrong one. And so I beg the reader to judge mildly of this attempt at a reasonable classification of the Hydro- medusae. 242 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, THE SCYPHOMEDUS2E OF THE SOUTHERN HEMISPHERE. By R. von Lendenfeld, Ph.D. Part II. III. Ordo. — Cubomedus^e. Haeckel, System der Medusen. Seite, 423, 1879. Ckarydeidse. Gegenbaur, 1856. Marsupialidse. Agassiz, 1862. Conoraedusse. Haeckel, 1878. Lobopkora. Claus, 1878. Acraspede with 4 perradial niai'ginal bodies, wkick contain an acoustic club, witk Entodermal Otolitke sack, and one or more eyes ; 4 interradial tentacles or tentacle clusters. Gastral cavity with four wide perradial square pouches. Gonads four pair leaf- shaped bulges, which are fixed by their margin to the four interradial septa. They are developed from the Sub-umbral Entoderm of the pouches of the stomach. And they project free into their cavity. Family. Charybdeidce. Gegenbaur, 1856. Cubomedusae with 4 simple interradial tentacles, and 4 perradial marginal bodies, without any marginal flaps in the velarium, but with 8 marginal pouches, without arms in the 4 radial pouches. Genus. Procharybdis. Haeckel, 1879. Ckarydeidse witk 4 simple interradial tentacles witk Pedalia, simple velarium witkout velar-canals and without Frenula. Species. Procharybdis tetraptera. Haeckel, System der Medusen. Seite, 437. Tafel, XXV. Figuren, 3, 4. BY DR. R. VON LENDENFELD. 243 Umbrella nearly oval, 1£ times as high as broad, vertex flat ; the 4 side surfaces strongly curved. Gastral cavity flat with 4 large oval mouth flaps. In the interradial elongated corners of the base of the Gastral cavity there are 4 pairs of wing-shaped Phacellse, every one hand-shaped and split in 20 — 30 filaments. Margin of the Umbrella wit h 8 flat adradial gallert-flaps. Velarium simple, narrow, continuous. The distance of the niches of the sense organs from the margin of the Umbrella is about the same as that of the Pedalbase. Four Pedalia very large, about as long as the height of the Umbrella ; leaf-shaped, with 2 large wings. The Abaxial wing reaches nearly to the middle of the interradial margin of the Umbrella. The Axial wing is very narrow above, and very broad and deeply cut out below. Four tentacles are higher than the height of the Umbrella. Size : Breadth of Umbi'ella, 20 mm. Height of Umbrella, 30 mm. Locality : Indian Ocean ; Sunda, Archipel. Rabbe. Species. Procharybdis Jlagellata. Haeckel, System der Medusen. Seite, 438. (1) Marsupialis flagellata, Lesson, 1843, Acalephes, p. 278. Umbrella conic, stubbed above. The height twice the width ; 4 side surfaces strongly curved. The 4 interradial sides rounded and a little projecting. Gastral cavity 1 Margin of Umbrella continuous with 8 laps. Velarium simple, narrow, continuous. The distance of the niches of the sense organs to the margin of the Umbrella is about half the distance of the pedal base. 4 Pedalia lancet shaped and half as long as the height of the Umbrella, with very narrow wings. Tentacles sevei^al times as long as the height of the Umbrella. Size : Breadth of Umbrella, 20 mm. Height of Umbrella, 40 mm. ; Ontogenesis unknown. Locality: North Coast of Australia : Torres Straits. Weber (New Guinea. Lesson *?) 244 THE SCYPHOMEDUS.E OF THE SOUTHEKN HEMISPHERE, Species. Procharybdis cuboides. Haeckel, System der Medusen. Seite, 439. Umbrella nearly cubic, stubbed above, the same height as breadth. Gastral cavity square, quite flat with 4 short mouth flaps. 4 Phacelles bipartate, with very short and numerous Gastral filaments. Twice as broad as their interval. Margin of Umbrella hardly flapped. The distance of the niches of the sense organs to the margin of the Umbrella about half the distance of the pedal base. Velarium pretty broad, quite simple, plaited. Pedalia nearly lancet-shaped, broadest in the middle, with two narrow wings, half the height of the Umbrella. Tentacles about as long, swollen to a roundish knob at the end. Size : Breadth of Umbrella, 35 mm. Height of Umbrella, 35 mm. Ontogenesis unknown. Locality : Tropic Zone of the Pacific Ocean ; Sandwich Islands. Ballier. Species. Procharybdis securigera. Haeckel, System der Medusen. Seite, 640. Umbrella nearly cubic, stubbed above, as high as broad. Gastral cavity quadrate, flat, with 7 triangular mouth flaps, 4 pair wing- shaped Phacellse, every one split in 10 — 20 filaments. Margin of Umbrella slightly 8 flapped. The distance of the niches of the sense organs from the margin of the Umbrella is the same as their distance from the pedal base. 4 Pedalia axe-shaped, half as long as the height of the umbrella. 4 Tentacles which are longer than the height of the Umbrella swollen at the base to a roundish knob. Size : Breadth of Umbrella, 40 mm. Height of Umbrella, 40 mm. Locality : Pacific Coast of Central America. Fuchs. Genus. Charybdea. Peron et Leseur. Charybdeide with 4 simple interradial tentacles, with Pedalia, suspended velarium (velar-canals with 4 perradial Frenula). Gastral cavity flat and low, without broad mesenteria. 4 horizontal groups of filaments, single or double, fascicular or pencil-shaped, onlv on the interradial corners of the fundus. BY DR. R. VON LENDENFELD. 244 Species. Charybdea alata. Reynaud. Haeckel, System der Medusen. Seite, 441. Charybdea alata. Reynaud, 1830. Lesson's Centurie Zoolo- gique, p. 95. PI. 33. Fig. 1. Marsupialis alata. Lesson, 1843. Acalephes, p. 278. Tamoya alata. L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 174. Umbrella conic, about as high as broad. Gastral cavity very small, scarcely half as broad as the Umbrella-radius. Gastral cavity simple. Four Phacelhe simple pencil-shaped, scarcely half as broad as their interstices. The distance of the niches of the sense organs from the margin of the Umbrella is J as great as their distance from the pedal base. Velarium narrow in every quadrant with 6 simple velar canals. Pedalia lancet-shaped, nearly as long as the Umbrella is high, with rather broad wings. Colour : Gastral cavity blue, accoi'ding to Eeynaud. Size : Breadth of Umbrella, 30 mm. ; height of Umbrella, 33 mm ; Ontogenesis unknown. Locality : South Atlantic Ocean, Reynaud, South Africa. W. Bleek. Genus. Tamoya. Fritz Miiller, 1859. Charybdeide, with 4 simple interradial tentacles, pedalia, suspended velarium, (with velar-canals and 4 perradial Frenula,) Gastral cavity large and deep, connected with the Sub-umbrella, by 4 broad perradial mesenteria. Four filament groups of vertical rows of threads, or brush-shaped bands which represent the inter- radial middle-lines of the sides of the Gastral cavity. Species. Tamoya haplonema. Fritz Miiller, 1859. Haeckel, System der Medusen, Seite, 443, 1879. Tamoya haplonema, Fritz Miiller, 1859; Abhandl. Naturf. Ges. Halle. Bat. V, p. 1., Taf. I.. IT. Tamoya haplonema, L. Agassiz, 1862 ; Monogr. Acal. Contrib. IV., p. 174. 246 THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE, Umbrella nearly quadrangular-prismatic, stubbed at the top, more than J as high as it is broad. Gastral cavity nearly globular, occupying the upper half of the Sub-umbrella-cavity. Twice as high as the infundibuliform mouth-tube, which is split below into 4 short triangular mouth-flaps ; 4 Phacellte simple interradial rows of thread, which pass through the upper § of the Gastral side of the cavity. Velarium broad, with numerous dendritic ramified canals. Pedalia in the form of clubs, twice as long as broad, about £ as long as the height of the Umbrella, spreading towards the base, two winged with broad meridial- wings. Size : Breadth of Umbrella, 120 mm. Height, 150 mm- Ontogenesis unknown. Locality : Coast of Brazil, Desterro, Santo Catharina. Fritz- Miiller. Species : Tamoya bursarice. Haeckel. Haeckel, System der Medusen. Seite, 444, 1879. Bursarius cythereso, Lesson, 1829 \ Voyage de la Coquille, Zoophytes, p. 108, pi. XIV., fig. 1. Bursarius cythereaB, L. Agassiz, 1862. Monogr. Acal. Contrib. IV, p. 174. Umbrella semi-spherical, the upper third curved, the other thirds cubic, \\ as high as broad. The semi-spherical cupola and the 9 quadratic side-surfaces are papillous, sprinkled with large nettle-knobs. The 4 corner pillars, half as broad as the side-surfaces, are divided into two parts by a deep furrow, and longitudinally finely ribbed. Margin of Umbrella only slightly thickened, divided into many triangular prismatic ridges by deep cuttings. From which 6 — 8 are on each of the 4 side-surfaces. Pedalia oval, three-cornerd, l£ as long as the sub-umbrella cavity, the dorsal margin wing-shaped, rising from the margin of the Umbrella. Size : Breadth cf Umbrella, 70 mm. ; height of Umbrella, 100 mm. ; Ontogenesis unknown. Locality : New Guinea, Kawack. Waigion. Lesson. BY DR. R. VON LENDENFELD. 247 Species. Tamoya gargantua. Haeckel. Haeckel, System der Medusen. Seite, 444. Beroe gai'gantua, Lesson, 1829 ; Voyage de la Coquille, Zoo- phytes, p. 261, pi. XV., fig. 1. Epomis gargantua, Lesson, 1S43, Acalephes, p. 262. Umbrella quadrangular-pyramidal, twice as high as broad. Diameter of the opening of the Umbrella 3 times as large as that of the stubbed summit. Exumbrella with 16 deep longitudinal furrows, by which 16 convex divisions of nearly the same breadth are formed. Gastral cavity nearly globular, occupying the upper third of the Sub-umbrella cavity, 4 Phacelke, simple interradial rows of threads along the sides of the Gastral cavity. Velarium broad, with numerous, dense slightly branched canals. Pedalia nearly sickle-shaped, with broad convex abaxial wings, narrow concave abaxial-wings, \ as long as the Sub-umbrella cavity. Size : Breadth of Umbrella 80-100 mm. ; height, 200 mm. Ontogenesis unknown. Locality : Tropical part of the Pacific Ocean, Tahiti, Lesson, Samoa, Weber. Family. Chirodropidce. Haeckel, 1879. Cubomeduste, with 4 interradial tentacle-bundles and 4 perradial marginal bodies ; with 16 marginal pouches in the marginal flaps of the velarium and 8 umbral arms in the 4 radial- pouches. Genus. Chirop>salmus. L. Agassiz, 1862. Chirodropidag, with 8 simple finger-shaped pouch-arms on the Umbrella-wall of the 4 radial-pouches, with 4 hand-shaped Pedalia, which possess numerous tentacles, and with S leaf- shaped Gonads. Species. Cliriropsalmus zygonema. Haeckel. Haeckel, System der Medusen. Seite, 641. Umbrella quadrangular pyramidal, stubbed above, 1^ times as high as broad, with the suspended velarium. Mouth-tube small, with 4 flaps, half as long as the roundish Gastral- 17 248 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE. pouch, the side-walls have 4 interradial arched Pkacellae. The two pouch-arms oval and very small ; 4 Pedalia leaf-shaped, two- edged, not symmetrical, about ^ as long as the height of the Umbrella, every one with 2 short gallert-processes. Altogether 8 tentacles. Size : Breadth of the Umbrella, 40 mm. ; height of Umbrella, 60 mm. Locality : South Atlantic Ocean. Smith. Species. Chiroj>salmus quadrwmanus. L. Agassiz. Haeckel, System der Medusen. Seite, 447- Chiropsalmus quadrumanus, L. Agassiz, 1862 ; Monogr. Acal. Contrib. IV., p. 174. Tamoya quadrumana, Fritz Muller, 1859; Abhandl. Naturf. Ges. Halle, p. 1., Tef. I. Umbrella bell-shaped, nearly semi-spherical, together with the suspended velarium scarcely as high as broad. Mouth-tube large, quadrangular pyramidal, split into 4 strong triangular mouth- flaps, higher than the nearly globular gastral pouch, which contains 4 interradial crooked arched rows of Gastral filaments. Two pouch-arms on the umbral-wall of each radial-pouch, near their entrance, very large, fingershaped, simple and more than half as long as the pouch itself. Four Pedalia hand-shaped, not symmetrical, nearly as long as the height of the Umbrella, every one with 10 narrow gallert-processes. Altogether 40 long tentacles. Size: Breadth of the Umbrella, 120 mm.; Height of the Umbrella, 130 mm. Ontogenesis unknown. Locality : Coast of Brazil, Desterro Island, S. Catharina. Fritz Muller. Genus. Cliirodro'pus. Haeckel. Chirodropida?, with 8 quadripartite, half feathered pouch-arms on the umbral-wall of the 4 radial-pouches, with 4 hand-shaped Pedalia, which possess numerous tentacles, and with 8 grape-like Gonads. BY DR. R. VOX LF.XDEXFELD. 249 Species. Chirodropus palmatus. Haeckel. Haeckel, System der Medusen. Seite. 448. Umbrella quadrilateral-prismatic, vaulted above like a bell, with the suspended velarium 1^ times as high as broad. Margins strongly projecting, sides flat. Mouth-tube with 4 flaps, scarcely half the height of the oval Gastral pouch. Both pouch arms on the umbral-wall of each radial-pouch are aduate in their two upper thirds, and are only free in the lower part and split into a great many filaments. Four Pedalia hand-shaped, not symmetrical, very large, neaily as long as the height of the Umbrella, each with 21 long and broad band-shaped gallert- processes. Altogether 84 long tentacles. Size: Breadth of Umbrella, 70 mm. ; height of Umbrella 100 mm. Ontogenesis unknown. Locality : South Atlantic Ocean, not far from the Island St. Helen. Levasseur. Species. Chirodropus gorilla. Haeckel. Haeckel, System der Medusen, 448. Umbi"ella bell-shaped, nearly semi-sph?erical Together with the suspended velarium 1 \ times as high as broad, margin slightly projecting, side curved. Mouth-tube quadrilateral-pyramidal nearly as high as the globular gastral-pouch. Both pouch-arms on the umbral-wail of the radial-pouches are adnate in their upper third, in the lower part they hang freely in the pouch, and are split into numerous filaments. Four Pedalia hand-shaped, not symmetrical scarcely as high as the height of the Umbrella, each with 9 long narrow gallert-processes. Altogether 36 tentacles. Size : Breadth of Umbrella, 120 mm.; height, 150 mm. Ontogenesis unknown. Locality : Coast of New Guinea, Ckiiichozo Loango. Falkenstein. 250 on some fossil plants from dubbo, n. s. wales, On some Fossil Plants from Dubbo, New South Wales. Plate IX. By the Rev. J. Milne Curran, F.G.S. While attempting to determine the geological position of the so-called Hawkesbary Sandstone at Dubbo, I have been gradually led to study the fossil plants which are so abundantly represented in the district. A few yeai's ago I submitted my collection of fossils to the Rev. J. E. Tenison- Woods, who identified the species already known at that time. Shortly afterwards he gave a diagnosis and figures of all the new species in a paper entitled, " The Fossil Flora of the Coal Deposits of Australia," published in Vol. VIII. of our Proceedings. The following is a list of the fossil plants described therein : Filices. Sphenopteris crebra, Ten. -Woods. Ballimoi'e. Sphenopteris glossophylla- Ten. -Woods. Baltimore. Neuropteris australis, Ten.-Woods. Baltimore. Thinnfeldia odontopteroides, Morris. Dubbo. Thinnfeldia media, Ten.-Woods. Dubbo. Alethopteris Currani, Ten.-Woods. Ballimore. Alethopteris concinna, Ten.-Woods. Ballimore. Merianopteris major, Feistm. Ballimore. Conifers. Walchia milneana, Ten. -Woods. Ballimore. Since the publication of the paper referred to, I have collected fossils from many parts of the district. Cf these some are well- known species, but others cannot be referred to any hitherto described Australian forms. Odontopteris macrophylla, sp. now Plate IX., fig. 3. Frond pinnate and bipinnate. Pinnules more or less opposite, oblkpiely ovate to ovate-acuminate, free, obliquely inserted by the whole base. No costa. Veins fine, all arising from the rachis, BY THE REV. J. MILNE CURRAN, F.G.S. 251 dichotomous, diverging as they ascend, and numbering 30 to 33 at the margin. Length of longest pinnule, 10; width of base, 9. Length of specimen, 67 : all millimetres. Loc. Dubbo. This beautiful and undoTibted species of Odontopteris (Brong- niart) is very different from M'Coy's 0. microphylla, from which it is easily distinguished by its greater size and general habit. The Dubbo species was found in a shaft sunk on the Railway line at 275 miles 25 chains. It is common in a dark carbonaceous shale, associated with Thinnfeldia odontopteroides, Hymenophyllites dubia, and Alethopteris australis. I am of opinion that many of the very fine impressions on the Dubbo Sandstones, considered to be some species of Thinnfeldia, can be referred to this genus. On Plate IX., fig. 4a, I have reproduced a pinnule of Thinnfeldia odontopteroides from Dr. Feistmantel's " Palaeozoische und mesozoische Flora des ostlichen Australiens," for comparison with a pinnule of Odontopteris. In mere impressions or casts, showing no trace of the venation, the one cannot be distinguished from the other. The differences, however, are very great. In Thinnfeldia the veins arise, partly from one, which is almost median, and partly from the rachis ; while in Odontopteris all the veins come direct from the rachis. Alethopteris australis. Morris (as Pecopteris). Refs — Strzelecki, Ph. Desc. of New South Wales, pi. VIII., figs. 1, 2, 2a. M'Coy, Pake. Vict., pi. XIV, fig. 3, p. 17. Feistmantel quotes this fern from the Clarence River — the only locality hitherto known for it in N.S.W. There can be no doubt as to its identity ; as in the case of Thinnfeldia and Hymeno- phyllites. I have been able to mount some pinnules on microscopic slides, so that the venation can be followed as easily as in a recent fern. Loc. Same as proceeding. 2~)2 ON SOME FOSSIL PLANTS FROM DUBBO, N. S. WALES, TlIIXXFELDIA ODONTOPTEROIDES. Feistm. PI. IX., fig. 4. Refs.— Proc. Linn. Soc, N.S.W., Vol. VIII., p. 1C2. This fossil plant has been described and figured in almost every variety by Dr. O. Feistmantel in the work already referred to. As Feistmantel's papers are not easily procurable, and as Thinn- feldia is (in Australia) a recognised characteristic mesozoic fossil, I herewith present a figure of a specimen, from Garensey's Quarry, Dubbo, where it is very common. It is confined to a particular bed — a sparsely micaceous, finely bedded, friable sandstone. It occurs, either in the shape of sharply defined casts, which show Thinnfeldia to have been a plant with stout coriaceous pinnules, or as a red impression (peroxide of iron), which is reduced to dust by exposure. In a shaft sunk on the Railway, about three miles from the Quarry, Thinnfeldia fossils are found in a remarkable state of preservation, in a black carbonaceous shale. The shale may be truly described as consisting almost entirely of plant remains. As the shale is taken out fresh it is not easy to see the fossils, but as the stone weathers they peel off in flakes. It is only necessary to steep them in water, and pinnule separates from pinnule and rachis from rachis so perfectly, that they may be mounted on microscopic slides as translucent objects. Many of them can readily be used as negatives to obtain nature-printed heliotypes. PL IX., fig. 4, is an enlarged copy of one. Some of the pinnules are studded with minute dots, which may be stomata. Although I have examined more than 50 specimens by transmitted light, I have never met with anything which could be considered as pointing to the mode of fructification, of which nothing is known That this should be so, is remarkable, notwith- standing all that has been written, and the great number of plants that have been examined during the last forty years. It lends some weight to the opinions of Ettingshausen and Andrea, who placed Thinnfeldia with the Conifers. It is not easy to see the reason for this, for it appears amongst ourselves co be a settled question, that Thinnfeldia was a fern. 1 have to add the BY THE REV. J. MILNE CURRAN, F.G.S. 253 following localities as new : — Beni, Talbragar R., Macquarie R., between Wellington and Dubbo, 16 miles from the latter place. In both instances the specimens were not perfect enough for specific determination. Hymenophyllites dubia. Nov. sp. PI. IX., figs. 1 and 2. This cannot, with the material in hand, be distinguished from Sphenopteris digitata of Phillips. (See Geology of Yorkshire. 2nd Edit. Part I. Plate VIII., figs. 5 and 6.) Nothing was known of the venation of the Yorkshire species. In the Dubbo species, however, a nervure can be made out, which is divided and continued into each lobe. It certainly belongs to the Sphenop- teridse and for the reason stated, I consider it a species of Hynenophyllites. As more perfect specimens will doubtless come to hand, I content myself for the present with figuring the species. Phillips' species is derived from the sandstones and shales of Gristhorpe and Scalby (Jurassic.) Loc. From a well, West Dubbo. CYCADACE^E. PODOZAMITES. Sp. Prof. M'Coy described (Pal. Vict., p. 33, pi. 8, figs. 1, 2, and 5) a species of Podozamites which was associated with Alethopteris Austrcdis, and with which the Dubbo specimen will, I think, be found identical. I collected only one example, and that a fragment, but parallel nerves rapidly constricted at the base were easily noticeable, and at once separate it from Zamites — the one other form which it approaches. Loc. Railway shaft, associated with Thinnfeldia odontopteroides, Alethopteris Austrcdis, Odon- topteris macrophylla and Podozamites ? CONIFERS. Walchia piniformis (V). Sterengberg. Refs. Fl. d. Vorw. i. p. 22. Goeppert, Foss. Flor. de Perm., pi. 49, fig. 13. Twigs of this are found in water-worn pebbles of an indurated fireclay in the Talbragar R. It differs from Wcdchia Milaeana, 254 NOTES AND EXHIBITS. Ten.- Woods, in having its leaves linear to lanceolate and curved inwards at the apex. A few of the specimens show that the stems were flexible, reminding one of some of the Lycopodiaceas. One species can hardly be distinguished from one figured by Mr. Twelvetrees, from the Upper Permian of Eastern Russia. (Qt. J. Geol. Soc, Lond., Vol. 38, p. 498, pi. 21, fig. 4.) In conclusion I may remark that there are some forms which we should expect, which are not as yet recorded from Dubbo, notably Tmtiopteris. With the foi-egoing list, imperfect as it is, it would be an easy matter to make some attempt to correlate the Dubbo and Ballimore beds with other well-known formations ; this I propose to attempt in another paper. Explanation of Plate IX. 1. — Hymenophyllites dubia. 2. — A few lobes of same as seen by transmitted light. 3. — Odontopteris macrophylla and Thinnfeldia. 4. — Thinnfeldia odontopteroides, from Dnbbo. 4a. — Pinnule from Feistmantel. NOTES AND EXHIBITS. Mr. Ramsay exhibited a fine collection of Marine animals in illustration of the new and excellent methods of mounting and preserving specimens in use by Senor Lo Bianco, at Dr. Dohrn's Zoological Station, Naples. Among the exhibits were Trachypterus Uenia, Torpedo ocellata, Pennaria Carolinii, Eudendrium ramosum, Zoobotryon pellucidum, Pennatula phosphora, Autidon rosacea, Ghromodoris elegans, Pleurophyllidea lineata, Pyrosoma elegans, Cestus Veneris, Rhizostoma pulmo, and many other beautiful preparations. The President exhibited a portion of the lower jaw of a Diprotodon which had been found near Armidale by Mr. W. M. Harris. It was interesting to note the occurrence of the remains of this gigantic extinct marsupial on the summit of the Great Dividing Range as well as on the low-lying plains of the Darling District. WEDNESDAY, 30th APRIL, 1884. The Vice-President, Dr. James C. Cox, F.L.S., in the chair. MEMBER ELECTED. Layman M. Harrison, Esq., of Sydney. DONATIONS. " Mittheilungen aus der Zoologischen Station zu Neapel." Band Y, Heft 1. From the Director. "On the Origin of the Flora and Fauna of New Zealand." By Prof. F. W. Button, F.G.S., &c. From the Author. "Journal of the Royal Microscopical Society of London." February, 1884. Also, " List of Fellows, &c, 1883. From the Society. " Transactions of the Entomological Society of London." 1883, Part Y. From the Society. "Nests and Eggs of Australian Birds." By Archibald J. Campbell, Melbourne. 8vo, 1883. Fiom the Author. " Bulletin of the Museum of Comparative Zoology at Harvard College." Yol. XL, No. 9, 1883. From the Curator. " Report of Progress of the Geological and Natural History Survey of Canada, for 1880-81, 1882." 1 Yol., 4to. With accompanying Maps, 1883. " Catalogue of Canadian Plants." 1883. From the Director of the Survey. " Science." Yol. III., Nos. 53 to 57, 17th February to 7th March, 1884. From the Editor. " Tijdschrift voor Entomoiogie." Yol. 26, Parts 3 and 4, 1882-83. From the Entomological Society of the Netherlands. 256 ON THE PRESERVATION OF TENDER MARINE ANIMALS, " Supplement to descriptive Catalogue of the Fishes of Aus- tralia." By the Hon. William Macleay, F.L.S. From the Author. " Victorian Naturalist." Vol. I., No. 3., March, 1884. From the Field Naturalists' Club of Victoria. A very large and valuable collection of the publications of Belgian Scientific Societies. From M. Th. Lefevre, Secretary of the Royal Malacological Society of Belgium. "Feuille des Jeunes Naturalistes." No. 161, March, 1884. From the Editor. " Me moires de la Societe de Fhysique et d'Histoire Naturelle de Geneve." Tomes XXIII. to XXVII. and XXVIII., Part I. 1873 to 1882, 4to. From the Society. " Linnaei Genera Plantarum." 1 Vol., 8vo., 1764. From Thomas Whitelegge, Esq. " Entomologisk Tidschrift pa foranstaltande af Entomologiska foreningen i Stockholm." Arg. 4, Heft. 1, 2, 3 and 4, 8vo, 1883. From the Society. PAPERS READ. ON THE PRESERVATION OF TENDER MARINE ANIMALS. By R. Von Lendenpeld, Ph.D. I shall endeavour here to give a few hints on this subject which may be of service to those of our members, who have no access to the Zoological Journals in which such methods of preserving are described. I do this in consequence of a wish expressed at the March meeting at the Linnean Society of N.S.W. Medusa?, Actiniae, Alcyonidae, and particularly also Syphono- phora and Cnetophora are so tender, and contain in parts of their bodies such a great percentage of water (in Aurelia as much as 97% !) that it is difficult to preserve them without their shrinking. BY II. VON LENDENFELD, PH.D. 257 Like other specimens, these also should be kept in strong non- methylated spirits of wine (70-80%), or in a mixture of alcohol and glycerine. But if they were placed in such a liquid immedi- ately on being caught, they would shrink to a shapeless mass and be useless. It is therefore necessary to harden them before placing them there. This hardening can be effected by the aid of com- pounds of heavy metals which act chemically on the Protoplasm in the cells, and harden it, thereby hardening the whole specimen. The metal itself, or its Oxide, is frequently precipitated in the Protoplasm, causing the whole to turn a dark colour. Osmic Acid, Chromic Acid, Chloride of Gold, Chloride of Palladium, Chloride of Quicksilver, Nitrate of Silver, and Chloride of Iron, are used for the above-mentioned purposes. The solutions in use are very weak, from 0-2 to 1% in strength, and the animal is immersed in them directly after having been removed from the seawater. The different solutions are allowed to act for some time, from one second to an hour or more as the case may be. Then the specimen is well washed in fresh water and placed in weak spirits (30 or 40%.) It is left there a short time, then placed in stronger spirits, and finally put into the strong spirits, (70-80%.) Different solutions are used to gain different ends. Osmic Acid preserves the Epithelia wonderfully, whilst Chloride of Gold and Picric Acid have a greater effect on that sort of Protoplasm which is met in Ganglia cells and Nerves, wherefore these are often used for the purpose of studying the latter. Chloride of Mercury (corrosive sublimate) is very much used and greatly recommended by many. Chromic Acid or Bichromate of Potassium, make the Frotoplasm yellow, and coagulate it in such a manner as to make it perfectly intransparent. Very transparent animals can, therefore, be made better visible by Chromic Acid. It must be used in very weak solution, and particularly carefully washed out before the specimens are placed in spirits. It preserves Epithelia exceedingly well, and is very useful to put fish in before preserving them in spirits. 258 ON THE PRESERVATION OF TENDER MARINE ANIMALS. Silver is reduced principally in the intercellular substance, and therefore used to demonstrate the cell margins. Chloride of Palladium is used for the same purposes as Gold. Besides preserving the animals in a natural state, it is also necessary to preserve them in an expanded state, and as all animals naturally roll themselves up and retract their soft appendages when placed in a poisonous solution, it is attended with great difficulty to kill them so rapidly that they have not time to retract. Sometimes it is possible to kill Hydroids and the Zooids of Corals with Osmic Acid so rapidly that they do not contract. Much more difficult this is with the Actinije (Sea anemones). The best way to preserve these latter in an expanded state, is to warm them to a temperature of about 43" C. Hereby they do not contract, and are lamed partially by the high temperature. They can then be chloroformed, the only poison which has any effect on them (1), and treated with Osmic Acid, or any of the other re-agents. The Osmic Acid is a high Oxide 03 05 of the Metal Osmium belonging to the Platina group with a specific weight of 22. It is exceedingly rare, and derived only from the remains of material out of which Platina has been obtained. F. E. Schulze was the first to introduce this substance into the Zoological Laboratories. And more discoveries are due to the application of this re-agent, than to any other. (1) The brothers Hertwig have shown that Curare and Cyanite of Potassium, and also Morphine do not affect them. A bit of Cyanite of Potassium half as big as a sea anemone placed in its stomach, does not kill it. THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE. By R. von Lendenfeld, Ph.D. Part III. — Conclusion. IV. ORDO. DlSCOMEDUS^E. Discomedusce. Haeckel, 1866. Phanerocarpce. Pschscholtz, 1829. Discophorce. Claus, 1879. (non Eschscholtz, 1829. non Agassiz, 1862.) SemaeostomecB et Rhizostomece. L. Agassiz, 1862. Acraspedge with 8-16 or more marginal bodies (always 4 perradial and 4 interradial, besides these sometimes several accessory) ; in each marginal body an acoustic vesicle with Entodermal Otolith-pouch, and often at the same time an eye. Marginal flaps, always 8 pairs primary (Ephyra-flaps), and besides often numerous accessory, (Velar-flaps). Tentacles some- times present, sometimes wanting. Gastral cavity surrounded by a circle of radial processes (8-16-32 or more), sometimes broad radial-pouches, sometimes narrow radial canals. Gonads 4, inter- radial folded bulges in the Sub- umbrella of the sides of the Gastral cavity, from the Entoderm of which they are developed (they disintegrate seldom into 8 adradrial bulges). They are sometimes pouch-shaped, sometimes protruding inwards into the central Gastral cavity, sometimes protruding outwards in hernia-shape into the Umbrella cavity. Umbrella flattened, orbicular. The ancestral form of all Discomedusaj is the Octomeral Ephyra. 260 THE SCYPHOMEDUSJE OP THE SOUTHERN HEMISPHERE, Family. Ephyridai. With broad radial-pouches, without terminal branch-canals. Discomedusse with simple, four cornered Manubrium, without mouth-ai'ms, with simple central mouth. Mostly 16 broad radial- pouches (8 ocular and 8 tentacular) rarely 16-32. "With these alternating as many short, solid tentacles. Mostly 16 (rarely 32-64) marginal flaps with or without simple flap-pouches, always without branched flap-canals. 4 interradial or 8 adradial Gonads in the Subumbrella wall of the Gastral cavity. Genus. Ephrya. Ephyridse with 8 marginal bodies, and 8 tentacles, with 1 6 marginal flaps without flap-pouches, and 4 interradial horse-shoe shaped Gonads. Species. Ephyra prometeor. Haeckel, System der Medusen. Seite, 482. Umbrella flat bell-shaped, 1^ times as broad as high. Marginal flaps oval, about as long as broad, and i as long as the radius of the Umbrella. Tentacles pointed, twice as long as the marginal flaps. 4 simple interradial Gastral filaments. 4 Gonads horse- shoe shaped without flaps and smooth. Size : Breadth of Umbrella, 8 mm. Height of Umbrella, 6 m.rn. Ontogenesis unknown. Locality : Coast of Australia. Weber. Species. Ephyra discometra. Haeckel, System der Medusen. Seite, 641. Umbrella flat, orbicular. Marginal flaps pentagonal, pointed, its tentacular side twice as high as its ocular side. Tentacles cylindrical, club like at the end, the same length as the radius of the Umbrella. In each of the 4 phacellae there are three Gastral filaments. 4 Gonads horse-shoe shaped, two-flapped. Genus. Palephyra. Ephyride with 8 marginal bodies and 8 tentacles, 16 marginal flaps and 16 flap-pouches (fork-shaped branches of the 8 ocular radial-pouches) and with 7 interradial horse-shoe shaped Gonads. BY R. VON LENDENFELD, PH.D. 261 Species. Palephyra antiqua. Haeckel, System der Medusen. Seite, 484. Umbrella nearly semi-spherical, with thick convex central disk, flat spread margin of disk, twice as high as broad. Marginal flaps narrow, oval, pointed, about half as long as the radius of brella. Tentacles as long as the radius of the Umbrella. 4 Gonads horse-shoe shaped with thin median arches and thickened lateral part. On each Gonad 6-8 thin Gastral filaments. Manubrium nearly cubic, hardly half as long as the radius of the Umbrella, without mouth flaps. Size : Breadth of Umbrella, 20 mm. Height of Umbrella, 8 mm. Locality : Indian Ocean, to the East of Madagascar. Genus. Zonephyra. EphyridsB with eight marginal bodies and 8 tentacles, 16 marginal flaps, and 32 flap-pouches (16 ocular and 16 tentacular) and 4 interradial horse-shoe shaped Gonads. Species. Zonephyra connectens. Haeckel, System der Medusen. Seite, 641. Umbrella flat orbicular with deep circular furrow. Manubrium as long as the diameter of the Umbrella, split into 4 oval triangular curved mouth-flaps in the distal third. 16 marginal flaps, nearly pointed, \ as long as the radius of the Umbrella. 8 tentacles about as long as the radius of the Umbrella. 4 Gonads horse-shoe shaped, two flapped. Size : Breadth of Umbrella, 10 mm. Height of Umbrella, 3 mm. Locality : Tropic zone of the Pacific Ocean. Weber. Genus. Nauplianta. Ephyride with 8 marginal bodies and 8 tentacles. "With 16 marginal flaps and 32 flap-pouches. (16 ocular and 16 tentacular), and 8 separate adradial Gonads, which are in regular groups, but not in pairs. 262 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, Species : Nauj)hanta Challengeri. Haeckel, System der Medusen. Seite, 487. Umbrella cap-shaped, with horizontal flat vertex and vertical side- wall, 1| times as broad as high. Exumbrella with deep circular furrows and 16 radial grooves. Margin of Umbrella with 16 pedalise (8 weak scapular and 8 stronger tentacular.) 16 marginal flaps oval nearly twice as high as broad, with deep clasp furrow, about £ as long as the radius of the Umbrella. Tentacles cylindrical, pointed, about as long as the radius of the Umbrella. Gonads 8, oval, thick, bulges twice as long as broad, their proximal halves a little broader than their intervals, their distal halves covered by the circular muscle. Size : Breadth of Umbrella, 12 mm. Height of Umbrella 8 mm. Locality : South Atlantic Ocean, not far from the Island Tristan deAcuhna. Lat. S. 32° 24'. Long., W. of Greenwich, 13° 5'. In 8,550 feet (1,425 fathom) depth. 16th of March, 1876. Station, 335 of the " Challenger " Expedition. "Wyville Thompson. Genus. Atolla. Ephyride with 16-32 (rudimentary) mai-ginal bodies, and the same number of tentacles, 32-64 marginal flaps, and 64-128 flap- pouches. 8 separate adradial Gonads, which are grouped in pairs. Rhopalia -pouches rudimentary, transformed into narrow glandular canals. Species. Atolla Wyvillei. Haeckel, System der Medusen. Seite, 488. Umbrella quite flat, orbicular, about 6 times as broad as high. Radius of disk of the Umbrella nearly twice as high as the margin of the Umbrella, divided from it by a very deep radial furrow. Manubrium contracted in the middle, 3-4 times as broad as high. Gonads grouped in pairs (in their circumference there are 8 elliptic pouches), their perradial intervals are shorter than the interradial. 19-22 (16-32 1) rudimentary marginal bodies, and as BY R. VON LEXDENFELD, PH.D. 263 many short alternating tentacles (half as long as the radius of the Umbrella.) Tentacle-pedalia broader and shorter than the rhopalar pedalia. The rhopalar flap canals rudimentary, much narrower and shorter than the tentacular canals. Marginal flaps elliptic, truncate with a broad membranous fringe. Size : Breadth of Umbrella, 58-66 mm. Height of Umbrella, 8-12 mm. Ontogenesis unknown. Locality : Antartic Ocean (Indian and Atlantic part). Wyville Thompson. Family. Liner g idee. Discomedusa? with simple quadrangular Manubrium without mouth-arms, and simple quadratic Mouth. 8 marginal bodies, 8 tentacles and 16 marginal flaps, with broad radial-pouches, and branched sack shaped flap canals, without ring canal. Genus. Linantha. Linergidse with 4 horse-shoe shaped interradial Gonads (ovaries the proximal arches of which are simple and not divided. On the Subumbrella there are small vesicular diverticals or Subumbral pouches. Species. Linantha lunulata. Haeckel, System der Medusen. Seite, 497. Umbrella cap shaped with horizontal upper surface and flat declining side-walls, twice as broad as high. Umbrella flaps oval, pointed, nearly twice as long as broad. Flap canals much bent and branched dendritically. The longest, \ as long as the flap itself. In every flap 60-70 cul-de-sac shaped, terminal branched. Ten- tacles cylindrical, nearly as long as the radius of the Umbrella, 1 \ times as long as the flaps. 4 Gonads simple horse-shoe shaped without interradial septum, with flat, crooked, nearly semi-circular proximal arches. Size: Breadth of Umbrella, 10 mm. Height of Umbrella, 6 mm. Ontogenesis unknown. Locality : Tropical Coast of the Pacific, South America, Galo- pagos Island. Fuchs. 18 264 THE SCYPHOMEJDUS^E OF THE SOUTHERN HEMISPHERE, Genus. Linerges. Linergidse with 4 horse-shoe shaped interradial Gonads, the convex proximal arches of which are divided into 2 adjacent wings by an interradial median septum. On the Subumbrella a double circle of 48 Subumbral-pouches (scrota1?). 16 larger proximal (under and between the Gonads), and 32 smaller distal (on the upper margin of the circle of the muscle.) Species. Linerges aquila. Haeckel. System der Medusen. Seite, 496. Umbrella cap-shaped with horizontal Exumbrella, and nearly vertical side-walls, 1^ times as bi-oad as high. Marginal flaps oval, a little longer than broad. Flap canals broad, hand-shaped, the longest (medial) half as long as the flap itself, in every flap 20-30 cul-de-sac shaped terminal branches. Tentacles cylindrical, at their ends club-like, 1| times as long as the flaps. 4 Gonads horse-shoe shaped, two- winged, both wings divergent, convex margin flat, on the concave side deeply incised. Size : Breadth of Umbrella, 18 mm. Height of Umbrella, 12 mm. Ontogenesis unknown. Locality : Indian Ocean, to the East of Madagascar. Rabbe. Genus. Liniscus. Linergidse with 8 separate adradial Gonads (ovarise) which are curved sickle-shaped or rectangular, and approach with their proximal ends, in pairs, in such a manner that they form a horse- shoe shaped group. On the Subumbrella there is a double circle of 48 Subumbrella pouches (scrota V). 16 larger proximal (under- neath and between the Gonads), and 32 smaller distal (at the upper end of the circle of muscles.) Species. Liniscus ornithopterus. Haeckel, System der Medusen. Seite, 497. Umbrella cap-shaped, with quite flat vortex and nearly vertical side walls, 1£ times as broad as high. Marginal flaps oval, l1 times as long as broad, covered with nettle-warts. Flap canals BY F. VON LENDENFELD, PH.D. 265 stretched straight and not bent out. The longest (medial) | as long as the flap. In eveiy flap 30-40 cul-de-sac shaped terminal branches. Tentacles cylindrical, conic at their ends, nearly twice as long as the flap. 8 Gonads wing-shaped. Both wings of each pair flapped, doubly broken in the inter-radius approaching nearly to touch. Size : Breadth of Umbrella, 20 mm. Height of Umbrella, 1 7 mm. Ontogenesis unknown. Locality : West Coast of the Tropic Africa, Angola, Congo. Briiggemann. Genus. Limtche. Linergidae with 8 adradial Gonads of the same shape, which are placed in the same intervals, and are approximated in pairs to 4 interradial groups. There is a threefold circle of Subumbrella- pouches (scrota'?), 16 larger proximal, 32 middling and 64 (or more) smaller distal. Species. Linuche Lamarckii. Haeckel, System der Medusen. Seite, 642. Umbrella nearly square with horizontal vortex and vertical side-walls, as high as broad. Marginal flaps oval, pointed, nearly twice as long as broad. Flap canal repeatedly dichotomous branched, with straight branches, the longest (medial) |- as long as the flap ; in each flap 20-30 cul-de-sac shaped terminal branchlets, Tentacles rod-shaped scarcely as long as the flaps. 8 Gonads globular, distributed at equal intervals. Size : Breath of Umbrella, 20 mm. Height of Umbrella, 20 mm. Locality : Atlantic Ocean, under the Equator. Smith. Family. Pelagidw. With a simple cross-shaped mouth and 4 folded perradiai moutharms, with simple broad radial-pouches, without branched distal canals, without ring-canal. Eight marginal bodies, 16 — 32 or more marginal flaps. 266 THE SCYPHOMEDUSjE OF THE SOUTHERN HEMISPHERE, Genus. Pelagia. Pelagidse, with 8 adradial tentacles (alternating with the 8 marginal bodies), and with 16 marginal flaps. Species. Pelagia panopyra. Haeckel, System der Medusen. Seite, 509. Pelagia panopyra. Peron et Lesueur, 1809. Tableaux des Meduses, etc., p. 349, N. 64. Pelagia panopyra. Eschscholtz, 1829. System der Acalephen, p. 73. Taf. VI., fig. 2, Pelagia panopyra. Lesson (p. p. !), 1830. Centurie Zool. p. 192, pi. 62, fig. 2. Pelagia panopyra. Brandt, 1838. Memoir. Acad. Petersb. Tom. IV., p. 382. Taf. XIV., fig. 1 ; Taf. XIV., A. fig. 1—5. Pelagia panopyra. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 164. Pelagia tuberculosa. Couthouy, 1862 ; in L. Agassiz. Contrib. IV., p. 164. (?) Pelagia Labiche. Eschscholtz, 1829. System der Acalephen, p. 78. (?) Pelagia Labiche. De Blainville, 1834. Actinologie, p. 302, pi. 40, fig. 3. (?) Pelagia Labiche. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 165. Medusa panopyra. Peron et Lesueur, 1807. Voyage aux Terres Australes, pi. 31, fig. 2. Dianaea panopyra. Lamarck, 1817. Hist. nat. An. s. vert. Tom. II., p. 507. Cyanea Labiche. Quoy et Gaimard, 1824. Voyage de l'Uranie, etc. Zoologie, p. 571, pi. 84, fig. 1. Umbrella semi-spherical, flattened above, nearly twice as broad as high. Kettle-warts of the Exumbrella small and scattered, elongated. Most dense on the margin of the Umbrella. Marginal flaps nearly quadratic, slightly crenated on the distal margin. Manubrium long and narrow, nearly twice as long as the radius of the Umbrella, 3 times as long as broad. Mouth-arms BY R. VON LENDENFELD, PH.D. 267 long and narrow, 1-J times as long as the manubrium, about 3 times as long as the radius of the Umbrella ; its membranous border is twice as broad as the thin cylindrical middle-rip, at its base. Colour : Variable, generally pale rose or violet. Mouth-arms more violet. Gonads more purple. Nettle-warts violet. Size : Breadth of Umbrella, 50 mm. Height of Umbrella, 33 mm. Ontogenesis unknown. Locality : Tropic zone of the Pacific Ocean, from Australia to Peru. Peron, Eschscholtz, Lesson, von Mertens, Couthouy, etc. Species : Pelagia papillata. Haeckel, System der Medusen. Seite, 509. Umbrella slightly vaulted. Orbicular 3 times as broad as high. Exumbrella thickly set, with high conic nettle-warts. Marginal flaps twice as broad as high, deeply crenated, nearly double flapped. Manubidum very long and narrow ; 8 times as long as broad, twice as long as the radius of the Umbrella. Mouth-arms short and narrow, a little shorter than the manubrium, scarcely as long as the breadth of the Umbrella. Its membrane boi'der narrow, nearly smooth, at the base narrower than the thin middle ribs. Size : Breadth of Umbrella, 40 mm. Height of Umbrella, 1 4 mm. Ontogenesis unknown. Locality : Indian Ocean. Schnehagen. Species. Pelagia discoidea. Haeckel, System der Medusen. Seite, 510. Pelagia discoida. Eschscholtz, 1829. System der Acalephen, p. 76, Taf. VII., fig. 1. Placois discoidea. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 125, 165. Umbrella quite flat, orbicular, 4 times as broad as high. Exumbrella smooth, without pi-qjecting nettle-warts. Marginal- flaps very flat, deeply crenated. Manubrium very short. Mouth- arms very long and narrow, 3 times as long as the radius of the Umbrella. Its membrane border broad, very much folded and curved, at its base several times bix>ader than the very thin cylindrical middle rib. 268 THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE, Colour : Pale reddish hue. Mouth-arms rose-coloured. Gonads whitish. Size : Breadth of umbrella, 70-80 mm. Height of Umbrella, 15-20 mm. Ontogenesis unknown. Locality : South Atlantic Ocean, near the Cape of Good Hope. Eschscholtz. Genus. Chrysaora. Pelagidpe with 24 tentacles (3 between 2 marginal bodies) and with 32 marginal flaps, 16 ocular, and 16 tentacular. Species. Chrysaora fulgida. Haeckel, System der Medusen. Seite, 514. Rhyzostoma fulgidum. Reynaud, 1830; in Lesson's Centime Zoologique, p. 79, pi. 25. Chrysaora Renaudii. Lesson, 1843. Acalephes, p. 401. Chrysaora Renaudii. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 166. Umbrella semi-spherical, twice as broad as high ; 32 marginal flaps short and broad, nearly semi- circular, with continuous margin. The 16 ocular and the 16 tentacular ones nearly of the same size, and equally projecting (octantes therefore with simple marginal arches), Radial pouch 1 Mouth-arms spread out from a narrow base, with only few folds, lancet-shaped, in the middle about half as broad as the radius of the Umbi'ella, 2-3 times as long as the diameter of the Umbrella. Tentacles about as long as the radius of the Umbrella. Colour : Umbrella yellowish brown. Star figure and marginal flaps reddish brown. Mouth-arms reddish, Gonads carmine. Size : Breadth of Umbrella, 300-700 mm. Height of Umbrella 100-200 mm. Locality : Cape of Good Hope, False Bay. Reynaud. Species : Chrysaora Blossevillei. Haeckel, System der Medusen. Seite, 514. Chrysaora Blossevillei, Lesson, 1829. Voyage de la Coquille. Zool., p. 115, pi. XIII., fig. 2. BY R. VON LENDEXFELD, PH.D. 269 Chrysaora Blossevillei. Lesson, 1843. Acalephes, p. 401. Lobocrocis Blossevillei. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 166. (!) Pelagia volutata. Coutliouy. Manuscr. in L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 166. (!) Zygonema volutata. L. Agassiz, 1862. Monogr. Acal. Contrib., IV, p. 127-166. Umbrella slightly vaulted to semi-spherical, twice as broad as high. 32 marginal flaps oval, all of the same size and equally projecting (octantes therefore with simple marginal arcb), Radial pouches 1 Mouth-arms lancet-shaped, strongly curved, shorter than the diameter of the Umbrella. Tentacles filiform, longer than the diameter of the Umbrella. Colour : Umbrella white, with yellow tinge, and brown design. Rust coloui'ed mouth arms. Size : Breadth of Umbrella 100 mm. Height of Umbrella, 40 mm. Locality : Coast of Brazil, Island Santa Catharina. Lesson. Species. Chrysaora plocamia. Haeckel, System der Medusen. Seite, 516. Cyanea plocamia. Lesson, 1829. Voyage de la Coquille. Zool., p. 116, pi. XII., fig. 4, Cyanea plocamia. Lesson, 1843. Acalephes, p. 385. Stenoptycha plocamia. S. Agassiz, 1862. Monogr. Acal. Contrib., IV, p. 162. Umbrella nearly semi-spherical, twice as broad as high. 32 marginal flaps nearly semi-circular. The 16 tentancular and 16 ocular flaps nearly the same size, equally projecting — (marginal arch of the octants therefore circular) — Radial pouches 1 Mouth - arms very broad and with many folds, in the middle nearly as broad as the radius of the Umbrella. 1J times as long as the diameter of the Umbrella. Tentacles shorter than the diameter of the Umbrella. 270 THE SCYPHOMEDUSiE OP THE SOUTHERN HEMISPHERE, Colour : Umbrella rust-colour, with yellow-brownish design. Month-arms without colour, with yellowish frills. Tentacles carmine. Size : Breadth of Umbrella, 100 mm. (and more). Height of Umbrella, 50 mm. Locality : Pacific Coast of South America, Peru, Lima, Song- allan. Lesson. Species. Chrysaora calliparea. Haeckel, System der Medusen. Seite, 516. (?) Cyanea calliparea. Reynaud, 1830. In Lesson's Centime Zoologique, p. 67, pi. XX. (?) Stenoptycha calliparea. L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 162. Chrysaora dinobrachia. Haeckel, 1877. Prodrom. System Med., Nr. 446. Umbrella slightly vaulted, 3 times as broad as high. 32 marginal flaps, kidney shaped, narrower at the base than at the distal margin. The 16 broader ocular flaps are less projecting than the 16 narrower tentacular ones (therefore the margin in the radius of the eye retracted.) 16 ocular radial-pouches oval, the same breadth in the middle,, and half the breadth on the distal margin of the 16 tentacular pouches. Mouth-arms curtain- shaped, very broad and long ; 3-4 times as long as the radius of the Umbrella, and curved. Tentacles flattened at the base, and longer than the diameter of the Umbrella. Colour : Exumbrella intensely reddish yellow, rays of the star- figure (with 32 radial stripes) and marginal flaps chestnut brown. Mouth-arms yellow speckled brown. Gonads yellow. Size: Breadth of Umbrella, 160-200 mm. Height of Umbrella, 50-100 mm. Locality : Indian Ocean. Reynaud, Zanzibar, Schnehagen. Genus. Dactylometra. Pelagidse, with 40 tentacles and with 48 marginal flaps. BY R. VON LENDENFELD, PH.D. 271 Species. Dactylometra lactea. Haeckel, System der Meclusen. Seite, 517. Dactylometra lactea. L. Agassiz, 1862. Monogr. Acal. Con- tributions to the Natural History of the U.S.A., IV., p. 166. Chrysaora lactea. Eschscholtz, 1829. System der Acalephen, p. 81. Taf., VII., fig. 3. Umbrella vaulted, semi-spherical. Mouth-arms short and broad, the 8 primary (adradial) and the 16 secundary Tentacles of equal length, 2-3 times as long as the breadth of the Umbrella. The 16 tertiary Tentacles much shorter, not so long as the basal distance between two long Tentacles. Colour : Milky-white, slightly rose coloured. Mouth-avms colourless. Tentacles pale purple. Marginal bodies yellow. Size : Breadth of Umbrella, 50-80 mm. Height, 30-60 mm. Locality : Atlantic Coast of South America, Rio Janeiro. (Eschscholtz.) Family. Cyaneid^e. Discomeclusee, with a simple cross-shaped mouth, surrounded by four adradial, folded mouth-arms. Gasti'al cavity, with 16 or 32 broad radial pouches, and branched coecal flap-canals, without a ring-canal. 8 or 16 marginal bodies, and 8 or more long hollow tentacles. Genus. Procyanea. Cyaneida3, with 8 marginal bodies and 8 adradial alternating tentacles of the Subumbrella. There are 8 pairs of flaps on the margin of the Umbrella. Species. Procyanea protosema. Haeckel, System der Medusen. Seite, 524. Umbrella slightly vaulted ; orbicular. 2-3 times as broad as high. Manubrium quadrilateral prismatic in the upper-half, in the lower-half split into 4 narrow lancet-shaped mouth-arms. Gonads, 4 narrow simple folded bands in the lower part of the gastral cavity, but not hanging down. 16 flaps of the margin of 272 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, the Umbrella pentagonal. 8 tentacles simple, strong, and larger than the diameter of the Umbrella. A good distance from the margin of the Umbrella. Size : Breadth of Umbrella, 40 mm. Height of Umbrella, 14-18 mm. Ontogenesis unkown. Locality : Indian Ocean, to the East of Madagascar. Rabbe. Genus. Medora. Cyaneide, with 8 marginal bodies, and 24 tentacles on the Sub- umbrella : 3 on the lower side of every flap. (Umbrella, with 8 main flaps and 16-32 secundary flaps.) Species. Medora reticulata, Haeckel, Das System der Medusen. Seite, 525. Medora reticulata — (et capensis?) — Couthouy, 1862. Manu- script of Wilke's, U.S. Exploring Expedition. Medora capensis — (reticulata?) — L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 118-163. Umbrella slightly vaulted, orbicular, mouth-arms ? Gonads ? Margin of Umbrella with 32 Haps, 8 pairs of narrow ocular flaps, and 8 pairs of broad tentacle-flaps. The margin of the 8 tentacle pouches with 2 broad flaps and 3 tentacles, (1 medial tentacle between two flap pouches and with two lateral flaps at its outer- margin.) Locality : Coast of Terra del Fuego, Orange Harbour, Cape Horn. Couthouy. Genus. Stenoptycha. Cyaneidse with 8 marginal bodies and 40 tentacles on the Sub- umbrella, 5 on the under side of each tentacle flap. Umbrella with 8 main flaps and 16-32 secondary flaps. Species. Stenoptycha rosea. Haeckel, System der Medusen. Seite, 525. Stenoptycha rosea. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 162. Cyanea rosea. Quoy et Gaimard, 1827. Voyage de l'Uranie etc., Zoologie, p. 570, pi. 85, fig. 1, 2. BY R, VON LENDENFELD, PH.D. 273 Umbrella slightly vaulted, semi-spherical 2-3 times as broad as high. Exumbrella set with warts, covered with pointed eleva- tions. Mouth-arms tender, l-ichly folded curtains, about as long as the radius of the Umbrella. The margin of the Umbrella has 16 small incisions of which the 8 ocular incisions are deeper than the 8 tentacular ones. 16 flaps quadrangular, truncate. There are 5 very large tentacles on the ventral side of each main flap, they are to 10 times as long as the diameter of the Umbrella. Colour : Pink. Margin of Umbrella and tentacles darker. Size : Breadth of Umbrella, 200 mm. Height of Umbrella, 100 mm. Length of tentacles neaxdy 2 metres. Locality : Port Jackson, Sydney. Quoy and Gaimard. Species. Stenoptycha Goethana. Haeckel, System cler Medusen. Seite, 642. Umbrella slightly vaulted, orbicular. Manubrium quadrangular- prismatic, about as long as the diameter of the Umbrella, split in the distal half into 4 oval curled mouth flaps. Gonads 4 curled. slightly bent bands in the lower Gastral wall. They are not suspended. Sixteen marginal flaps pentagonal and pointed. On the ventral side of each of the eight main flaps five tentacles. The middle one is much larger than the others and as long as the diameter of the Umbrella. The others only a third as long. Size : Breadth of Umbrella, 40 mm. Height, 20 mm. Locality : South Atlantic Ocean, Coast of Argentina. Smith. Genus. Desmonema. Cyaneidae with 8 marginal bodies and numerous tentacles, which are arranged in 8 adradial bundles on the Subumbrella; all tentacles of each bundle are in a single row. Margin of Umbrella with 8 main flaps, and 16-32 secondary flaps. Sppcies. Desmonema Annasethe. Haeckel, System cler Medusen. Seite, 526. Umbrella flat, cap shaped, 2-3 times as broad as high, mouth-arms curtain shaped, very tender and richly folded, nearly as long as 274 THE SCYPHOMEDUS.E OP THE SOUTHERN HEMISPHERE, the diameter of the Umbrella. Gonads are four richly folded pendant pouches, a little shorter than the radius of the Umbrella. Margin of Umbrella with 16 broad nearly pentagonal flaps. Tentacles uniserial in 8 bundles, in each bundle 5 larger, and on each side 4-6 smaller tentacles. Exumbrella depressed in the middle with 16 pinnate radial ribs. Size : Breadth of Umbrella, 100 mm. Height of Umbrella, 40-50 mm. Length of mouth-arms, 90 mm. Locality : South Atlantic Ocean, "West Coast of South Africa. Wilhelm Bleek. Species. Desmonema Gaudichaudi. Haeckel, System der Medusen. Seite, 527. Desmonema Gaudichaudi. L. Agassiz. Monogr. Acal. Contrib. IX,, p. 166. Chrysaora Gaudichaudi. Lesson, 1829. Voyage de la Coquille. Zoophyt., p. 114, pi. XIII., fig. 1. Umbrella semi-spherical, twice as broad as high. Mouth-arms lancet shaped as long as the diameter of the Umbrella, with narrow arm frills, which are not curtain shaped. Gonads not pendant. Margin of Umbrella with 8 (— \21) broad, rounded triangular, projecting flaps, between the 8 ( — 12 %) pair of narrow hidden scular flaps. Ex-umbrella with 8 ( — 12 1) pinnate radial ribs. Colour : Bright yellow, canals rust-i'ed, tentacles claret colour. Size : Breadth of Umbrella, 100 mm. Height of Umbrella, 40-50 mm. Mouth-arms, 100 mm. Locality : Falkland Islands (Soledad, Maluinen). and further south to Cape Horn. Lesson. Species : Desmonema pendula. Haeckel, System der Medusen. Seite, 528. Couthouya pendula. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 118, 163. Nerinea pendula. Couthouy, 1862. Manuscript of Wilke's " U. S. Exploring Expedition.'' BY R. VON LENDENFELD, PH.D. 275 Umbrella slightly vaulted, orbicular. Mouth-arm exceptionally long (several times longer than the radius of the Umbrella), with narrow arm-frills, which ai-e not curtain-shaped. Gonads not projecting much. Margin of Umbi'ella with 8 broad projecting tentacle flaps, between the 8 narrow clearly distinct ocular flaps. The 8 ocular-pouches nearly as long as the 8 tentacle-pouches. Locality : Coast of Terra del Fuego, Orange Harbour, Cape Horn, Couthouy. Genus. Cyanea. Cyaneidee, with 8 marginal bodies and numerous tentacles, which form 8 adradial bundles on the Subumbrella. There are- several rows of tentacles, one behind the other in each bundle. Margin of Umbrella, with 8 main flaps and 16-32 secundary flaps. Species. Cyanea Annaskala. Yon Lendenfeld, Zeitschrift fiir wissenschoftlich Zoologie, Band., XXXVII. Selte, 466, Taf. XVII.— XXIV. The Umbrella flaps are rounded and not broader at the end than at the base. Every main-flap (Ephyra-arm) consists of four flaps. Two smaller ocular flaps and two larger flaps at the sides. The Umbrella is 5-7 times as broad as high, depressed, with a few protruding nettle-warts in the centre of the Exumbrella. Ontogenesis. The embryos hang on to the Mouth-arms until they are nearly matured to young Scyphystomse, and then affix themselves to bodies in the water producing a long stalk with a chitinous Perisark, and eight arms. The Ephyra passes into the adult animal by a complicated metamorphosis. The Umbrella flaps are produced by fission. Colour : Umbrella and Tentacles colourless. Entoderm of the gastral cavity brown. Mouth-arms intensely purple. Genital organs in the male rose coloured, and in the female orange yellow. Size: 70-150 mm diameter of the Umbrella. Length of Tentacles, 300 mm. Locality : Port Philip. Von Lendenfeld. Abundant in January, February, and March. 276 THE SCYPHOMEDUSJE OF THE SOUTHERN HEMISPHERE, Genus. Drymonema. Cyaneida?, with eight sense organs, which lie remote from the margin of the Umbrella, in deep excavations. Tentacles scattered over the whole surface of the Subumbrella and arranged radially, branched ridges of the gallert lie between them. Drymonema Gorgo. Fritz Midler. Zoologischer Auzeiger. Band., VI., Seite, 220. The Mouth-arms are longer than in other species, attaining a length 2 or 3 times that of the breadth of the Umbrella. The Umbrella possesses 8 x 20 x 16=176 marginal flaps. Size : 300 to 500 mm., the diameter of the Umbrella. Tentacles, 10 meters or more. Locality : Rio de Janeiro. Fritz Mtillei\ Genus. Melusina. Cyanidse, with 16 marginal bodies and 16 bundles of tentacles, they are attached in several rows. Margin of Umbrella, with 16 main and 64 secundary flaps. Species. Melusina formosa. Haeckel, System der Medusea. Seite, 535. Umbrella, flat disc-shaped, 3-4 times as broad as high. Mouth - arms curtain-shaped, richly folded, longer than the diameter of the Umbrella. Gonads richly folded, suspended sacks, nearly as long as the Mouth-arms. Umbrella margin with 64 flaps, which are divided from each other by deep incisions. The 32 ocular flaps half as long as the 32 tentacular flaps. Tentacles numerous and long. Size : Diameter of Umbrella, 100 mm. Height, 32 mm. Locality : Pacific coast of South America. Station 299, of the " Challenger." W. Thomson. Family. FlosculiJu . Discomedusse, with simple xmbranched narrow radial canals and with a ring canal. With central mouth and mouth-arms at the end of a mouth tube. BY R. VON LENDENFELD, PH.D. 277 Genus. FlosGula. Elosculidse, with 8 marginal bodies and with 8 adradial tentacles, alternating with the organs of sense. 16 marginal flaps. Floscula Promethea. Haeckel, System der Medusen. Seite, 536. Tafel, XXXII., figs. 1, 4. Umbrella flat, slightly vaulted, 2-3 times as broad as high Exumbrella, with an oetoradiate pigmented star. Marginal flaps nearly pentagonal, as long as broad. Tentacles about as long as the diameter of the Umbrella, Mouth-tube about as long as the radius of the Umbrella, and of the same length as the lancet- shaped curled mouth-arms. Size : Breadth of Umbrella, 20 mm. Height, 8 mm. Locality : Indian Ocean, in the vicinity of the Cocos Islands. Rabbe. Floscula Pandora. Haeckel, System der Medusen. Seite, 643. Umbrella, semi-spherical, twice as broad as high. Exumbrella, with pigment-star. Marginal flaps oval, 1J times as broad as long. Tentacles as long as the radius of the Umbrella. Manu- brium half as long as the Umbrella radius, scarcely a quarter of the length of the narrow lancet-shaped mouth-arms. Size : Breadth of Umbrella, 30 mm. Height, 15 mm. Locality : Tropic Zone of the Pacific Ocean. Weber. Genus. Floresca. Flosculidse with 8 marginal bodies, 24 tentacles and 32 marginal flaps. Floresca Parthenia. Haeckel, System der Medusen. Seite, 538. Tafel, XXXIL, figs. 5, 8. Umbrella flat, barrett-shaped, twice as broad as high. Ex- umbrella with a pigment star of 16 rajs. Marginal flaps oval, pointed, broadest in the middle, twice as broad as long. Tentacles 278 THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE, 2-3 times as long as the diameter of the Umbrella. Manubrium 1 J- times as long as the Umbrella radius, the same length as the richly folded oval mouth-arms. Size : Diameter of Umbrella, 30 mm. Height, 3 mm. Locality : New Caledonia. Levasseur. Floresca palladia. Haeckel, System der Medusen. Seite, 539. Umbrella slightly vaulted, 3-4 times as broad as high. Ex- nmbrella with a pigment star of 1 b' rays. Marginal flaps nearly cpiadratic. Tentacles as long as the diameter of the Umbrella. Manubrium scarcely as long as the Umbrella. Umbrella radius not quite half as long as the 4 narrow lancet-shaped mouth-arms. Size : Breadth of Umbrella, 40 mm. Height, 12 mm. Locality : New Guinea. Koch. Family. Ulmaridce. Dicomedusa? with simple central mouth, and four mouth-arms, with branched, narrow, radial canals, and with a ring canal. Tentacles hollow and long. Genus. Ulma7'is. Ulmaridse with 8 marginal bodies, with 8 adradial tentacles, which alternate with the sense organs, and with sixteen marginal flaps. Uhnaris prototypus. Haeckel, System der Medusen. Seite, 445. Tafel, XXXIII. Figur. 1-4. Umbrella fiat, 2-3 times as broad as high. Manubrium square in its proximal part, in its distal part split into four oval mouth- arms, which are much curled and as long as the Umbrella radius. Gonads 4 narrow slightly bent bands, forming nearly a closed ring. Marginal flaps pointed, about as long as bx'oad. Tentacles as long as the diameter of the Umbrella. Size : Breadth of Umbrella, 30 mm. Height, 12 mm. Locality : St. Helena. Levasseur. BY R. VON LENDENFELD, PH.D. 279 Genus. Aurelia. Ulinarida? with 8 marginal bodies and with 8 broad adradial, sometimes bipartate velar flaps, each of which bears on its dorsal side, some distance away from the margin, a row of numerous short tentacles. Alternating with as many dorsal flaps. Mouth- arms simple. Species. Aurelia colpota. Haeckei System der Medusen. Seite, 555. Aurelia colpota. Brandt, 1838. Memoires de l'Academie Imp. des Sciences, St. Petersburgh. Tome IV., p. 370, tab. IX. Aurelia colpota. L. Agassiz, 1862. Monogr. of Acal, Contrib. to the Nat. H. of the U. S. A. Vol. IV, p. 160. Monocraspedon colpotus, 1835. Brandt, Prodrom. Descript. Animal. Mertens, p. 25. Umbrella flat or vaulted, 2-3 times as broad as high. 8 velar flaps of the Umbrella margin not protruding, divided from each other by small and shallow ocular incisions only. Mouth-arms slightly longer than the radius of the Umbrella. Much flapped. Deeply incised and broad at the base. Umbrella radius double the size of the radius of the Genital Organs. At every Genital bay, 5 canal roots. 16 anastomosing canal nets, with very elongate meshes. Colour : Pale reddish. Gonads and tentacles rose-coloured. Size : Diameter of Umbrella, 100-120 mm. Height, 40-50 mm. Locality : Indian Ocean, 35° S., 334° W. Mertens. Coast of Capland. Bleek. Species. Aurelia clausa. Haeckei, System der Medusen. Seite, 558. Aurelia clausa. Lesson, 1829. Voyage de la Coquille. Zool., p. 119. Aurelia clansa. L. Agassiz, 1862. Mongr. of Acal. Contrib. to the Natural pi. of the U. S. A. Vol. IV., p. 1 60. Claustra pissinbogue. Lesson, 1843. Acalephes, p. 78. Ocyroe lineolata 1 Peronet Leseur, 1809. Tableaux des Meduses, p, 355. 19 280 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, Cassioprea lineolata? Lamarck, 1817. Systeme des Animaux sans vertebres. Tome. II., p. 511. Umbrella semi-spherical, twice as broad as high. 1G velar flaps of the Umbrella margin protruding. Mouth-arms narrow, thin, and curled ; they coalesce at the base ; with a large oval, pointed lip-like thickening. The four labial thickenings can close (?) the entrances to the sub-genital pouches. Golozcr : Ovaries, canals, and tentacles rose coloured. Size : Breadth of Umbrella, 80-100 mm. Height, 40-50 mm. Locality : South Pacific Ocean, Port Proslin, New Ireland. Lesson. Australia (?) Peron. Aurelia coerulea. nov. sp. The Umbrella is very flat, about 5 times as broad as high, with 16 small ocular and 16 velar flaps, divided from the former by deep incisions, but from each other only by a shallow groove. The mouth-arms are broad and a little longer than the margin of the Umbrella. They are rounded at the end. The centrifugal branches of the canal system, divide at larger angles than in other species, so that the ramification has by no means a slender appearance. There are very few amostomoses only. It differs from Aurelia aurita, Lamark, by its broader mouth- arms, the margins of which are not curled, and by the stubby appearance of the canal system. In these respects Aurelia colpota, Brandt, resembles A. coerulea. The colour of our species is similar to that of A. aurita, but fainter and always decidedly blue. A. colpota also differs from our species in colour A. flavidula, Peron et Leseur, possesses flaps at the base of the mouth-arms, and has a yellow tinge. A. marginalis, L. Agassiz, has much smaller mouth-arms. A. hyalina, Brandt, again possesses lancet-shaped mouth-arms. A. labiata Chamisso et Eysenhardt possesses 16 velar flaps like our species, but these are divided from each other by deep incisions. In A. clausa, Lesson, the mouth-arms are narrow and curled, and the colour is red. In A. limbata, Brandt, there also are 16 very distinct velar-flaps, and the tentacles are brown. BY R. VON LENDENFELD, PH.D. 281 Similar in appearance, to one or other of these species, it still appears advisable to distinguish Aurelia coerulea from these. The main feature of our species are the broad and smooth mouth- arms. Colour : Transparent and blue. Only the hoof-shaped Gonads reflect the light, and appear white or light rose-coloured as in Aurelia aurita. Size : Diameter of Umbrella, 110 mm. Height, 20-30 mm. Ontogenesis : I have obtained a single Larva measuring 9 mm, this being similar to corresponding stages in Europseon Aurelias, we may suppose that the Ontogenesis of our species is similar to that of Aurelia aurita. Locality : Port Jackson. Von Lendenfeld. Genus. Aurosa. Ulruaridse, with 8 marginal bodies, and 8 broad adradial velar-flaps, each of which bears at its upper side, a little distance from the margin of the Umbrella, a row of numerous short tentacles alternating with the same number of much smaller dorsal flaps. Mouth-arms dichotomous. Species. Aurosa furcata Haeckel, System der Medusen. Seite, 559. Umbrella flat, orbicular. The 8 velar-flaps of the margin of the Umbrella slightly pi'ojecting, divided by small ocular-pouches. Mouth-arms a little longer than the Umbrella radius, very thick. Divided into two lobes by a deep incision in their distal part. Very much cmded at the margin. Umbrella radius twice as long as the genital radius. At every genital bay five canal roots con- nected with each other, and with the four perradial ocular canals by numerous Anastomoses. Canal-net dense with rounded meshes, which are half as large in the outer than in the inner zone. Size : Diameter of Umbrella, 80 mm. Height, 30 mm. Locality : Indian Ocean, Cocos Islands. Rabbe. 282 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, Family. Toreumidaz. Discomedusa) without tentacles and without central mouth, with four sub-genital cavities, and with ventral suction crisps on the mouth-arms. Genus. Archirhiza, . Toreurnidse, with 8 simple mouth-arms, neither branched nor furcated. Mouth-arms without vesicles and filaments with 16 radial canals and a ring canal, with 8 marginal bodies. Archirhiza aurosa. Haeckel, System der Medusen. Seite, 645. Umbrella flat, disc shaped, margin with 80 flaps, in every Octant 8 oval, pointed velar flaps between 2 broad triangular ocular flaps. Mouth-arms 1| times as long as the Umbrella-radius, conic, simple, with simple suction crisp. Size : Breadth of Umbrella, 50 mm. Height, 20 mm. Locality : New Zealand. Weber. Species. Archirhiza primordialis. Haeckel, System der Medusen. Seite, 565, Tafel, XXXVI. Figur. 1, 2. Umbrella slightly vaulted, hat-shaped or semi-spherical. 2-3 times as broad as high. Umbrella margin with 48 marginal flaps. In every Octant four large pointed velar flaps and two small ocular flaps. Mouth-arms about as long as the Umbrella-radius, cylindrical, simple and undivided ; on the axial margin with simple zig-zag shaped suction crisp. Size: Diameter of Umbrella, 40 mm. Height, 20 mm. Locality : Bass's Straits. Smith, Genus. Toreuma. Toreumida? with 8 feathered or trichotome branched mouth- arms. The upper arm is continued in the adradial main branch of the underarm. Numerous club-shaped vesicles between the arm- crisps. 16 radial canals, 8 marginal bodies. BY R. VON LENDENFELD, PH.D. 283 Toreuma theophila. Haeckel, System der Medusen. Seite, 566. Cassiopaea dieuphila. Peron et Leseur, 1809. Tableau des Meduses, p. 356. Cassiopaea theophila. Lamarck, 1817. Hist. Nat. Animaux sans Vertebres. Tome," II., p. 511. Rhizostoma theophila. Eschscholtz, 1829. System der Acal- ephen. Seite, 53. Polydoma theophila. L. Agassiz, 1862. Monogr. of the Acal. Contrib. to the Nat Hist, of the U. S, A. Vol. IV, p. 159, Umbi-ella semi-spherical 2-3 times as broad as high. Margin with 96 short coalescing flaps, in each Octant 10 velar flaps between two very small ocular flaps, Ex-umbrella roughly granulated, studded with warts with small oval white spots on the marginal flaps. 8 arms about as long as the Umbrella-radius. With 3 or 4 pair of broad and flat main branches. Between the clusters of crisps numerous, small, and 10 or 20 large club-shaped vesicles. The latter 2 or 3 times as long as the breadth of the main branches. Colour : Umbrella brownish-red, with white spots on the margin flaps. Gonads and vesicles white. Size : Diameter of Umbrella, 60-80 mm. Height, 20-30 mm. Locality ; N. \V Coast of Australia, de Witt's Land. Peron. Species. Toreuma thamnostoma. Haeckel, System der Medusen. Seite. 567. Umbrella flat, hat-shaped. 3-4 times as broad as high, with 120-160 marginal flaps which are short, truncate, and scarcely protrude. In every Octant 14-18 velar flaps between two very small ocular flaps. Ex-umbrella finely granulated with umerous white spots on a dark ground. Mouth-arms double as long as the Umbrella radius, branched in corymbose manner, with Q-8 pair of cylindrical main branches. Numerous small vesicles not larger than the marginal flaps. 284 THE SCYPH0MEDUS2E OP THE SOUTHERN HEMISPHERE, Colour : Umbi'ella, dark brown, with numerous white spots, dorsal side of arms white, ventral side brown. Vesicles white. Size : Breadth of Umbrella, 90 mm. Height, 30 mm. Locality : Indian Ocean. Schnehagen. Species. Toreuma Gegenbauri. Haeckel, System der Medusen. Seite, 645. Umbrella flat. In every Octant 8 rectangular velar, between two rudimentary ocular flaps. Ex-umbrella papillous, with an oval white spot on every flap. Arms 1-| times as long as the Umbrella- radius with 4-6 pair of flattened main branches. Between the crisps numerous small vesicles, one very large at the base of each arm, half as long as the arm. Size : Diameter of Umbrella, 60 mm. Height, 20 mm. Locality : Tropic part of Indian Ocean. Babbe. Genus. Gassiopca. Toreumidse, with 8 pinnate or trichotome branched mouth- arms. The upper arm extends as main branch to the end of the lower arm. Numerous club-shaped vesicles. 32 radial canals, 16 marginal bodies. Species. Cassiopea Andromeda. Haeckel, System der Medusen. Seite, 569. Cassiopea Andromeda. Eschscholtz, 1829. System der Acalephen. Seite, 43. Cassiopea Andromeda. Tilesius, 1829. Nova Acta. phys. med., N. C. Band., XV. Seite, 266. Tafel., LXIX., LXX. Cassiopea Andromeda. Milne Edwards, 1849. Cuvier, Begne. Animal Zoophytes, pi. LI., fig. 1. Cassiopea Forskalea. Feron et Leseur, 1809. Tableau des Meduses, p. 356. Medusa Andromeda. Forskal, 1775. Descript. Icones. Anim. itin. orient., p. 107, Tab. XXXI. Medusa Andromeda. Modeer, 1791. Nova. acto. Fhys. med. VIII. Appendix p. 30, Nr. 24. BY R. VON LENDENFELD, PH.D. 285 Umbrella flat. In each of the 16 paramers 3 velar flaps between two ocular flaps. Exumbrella, with 96 white radial spots. 16 large ocular and 16x5 smaller marginal spots. Arms broad and compressed, flat, scarcely as long as the Umbrella radius, with 2-3 pair of flat and short, curled main branches. Numerous small and 8-10 large vesicles on each arm. Colour : Very variable. Exumbrella reddish — or violet — brown, with white spots between the black radial stripes ; margin mostly blueish or violet, arms olive green or red brown, with white spots. Size: Diameter of Umbrella, 100-120 mm. Height, 20-30 mm. Locality : Red Sea. Tur., Forskal, Ehrenberg, Haeckel. India, Smith. Sundasea, Sumatra, Tilesius, Species. Cassiopea ornata. Haeckel, System der Medusen. Seite, 570, Tafel, XXXVII. Umbrella flat. In each paramere 3 velar flaps between two rudimentary ocular flaps. Exumbrella, with 96 radial white spots. 16 tongue-shaped ocular specs and 16x5 smaller marginal spots. Arms slender, cylindrical, a little longer than the Umbrella. Radius, with 3-4 slender, densely pinnate main branches. Numerous small vesicles. Size : Diameter of Umbrella, 100-120 mm. Height, 30-40 mm. Locality: New Guinea, Koch. Pelew Islands, Weber. Aus- tralia, Godeffroy. Species. Cassiopea depressa. Haeckel, System der Medusen. Seite, 572. Umbrella flat. Margin in each paramer, with 7 velar and two ocular flaps. Exumbrella without radial spots. Arms very flat shorter than the radius of the Umbrella, with 3-4 pair of short, broad and curled main branches. Very small white vesicles. Size: Breadth of Umbrella, 100-120 mm. Height, 15-20 mm Locality : Madagascar, Levasseur. Querimba Islands, Moss- ambique, Peters, 286 THE SCYPHOMEDQSJS OF THE SOUTHERN HEMISPHERE, Genus. Cepliea. Toreumidse, with eight bifurcated mouth-amis, the branches of which are simple and not dichotomous. The upper arm does not extend beyond the bifurcation. Between the suction crisps numerous filaments. 8 broad ocular canals, between which there are numerous narrow radial canals. Without ring canal. 8 marginal bodies. Species. Cephea fusca. Haeckel, System der Medusen. Seite, 575. Cephea fusca. Peron et Leseur, 1809. Tableau des Meduses, p. 361. Cephea fusca. Eschscholtz, 1829. System der Acalephen. Seite, 57. Cassiopea fusca. Dussumier, 1835. Mus6e. du Jardin des plantes. Nr. 111. Polyrhiza fusca. L. Agassiz, 1862. Monogr. of Acalephte. Contrib. to the Nat. Hist, of the U.S.A., Vol. IV., p. 156. Umbrella cap-shaped. Central dome flat, vaulted. Covered with 16 or 20 large conic excrescences. Divided from the thin margin of the Umbrella by a deep circular furrow. In every Octant 8 flaps which appear as secundary flaps of one large primary one which lies between the two ocular flaps. The two flat branches of the under arm three times as long as the simple upper arm. They do not reach to the margin of the Umbrella. Filaments numerous decreasing in size centrifugally. The longest as long as the Umbrella radius. Colour : Umbrella, dark brown. Exumbrella with 8 white radial stripes. Arms yellowish,, filaments white. Size : Breadth of Umbrella, 150 mm. ; height, 30 mm. Locality : N. W. coast of Australia, de Witt's land. Peron et Leseur. Malabar. Dussumier. Species. Cephea conifera. Haeckel, System der Medusen. Seite, 576. Tafel, XXXVI., figs. 3-6. BY E. VON LENDENFELD, PH.D. 287 Umbrella similar to a mitre. Central dome with a very thick wall, flat bell-shaped, thickly set with 20 or 30 large and many small gi-annlated conic protuberances. Deep circular groove. In every Octant 8 large rectangular coalescing velarflaps between two small deeply-set ocular flaps. The two compressed forks of the arm double as long as-the upper arm. Their distal ends projecting beyond the margin of the Umbrella. Filaments long and numerous. Four particularly stout ones on the Pillar-forks. Size : 100-120 mm. diameter of Umbrella ; height, 30-40 mm. Locality : Carolina Islands, Samoa Islands. Godeffroy. Genus. Polyrhiza. ToreumidsB with 8 bifurcate mouth arms, the branches are doubly bifurcate or dichotomous. The upper arm extends beyond the first bifurcation. Long brachial filaments between the crisps, 8 large ocular canals, and between them numei'ous smaller radial canals. Without evident ring canal. 8 marginal bodies. Species. Polyrhiza homopneusis. Haeckel, System der Medusen. Seite, 577. Homopneusis frondosa. Lesson, 1829. Voyage de la Coquille, Mollusques, plate. XII. Homopneusis frondosa. L. Agassiz, 1862. Monogr. of Acal. Contrib. to the Nat. H. of the U.S.A. Vol. IV, p. 159. Umbrella flat cap-shaped. The central Umbrella disc flat. Depressed in the centre. With 16 simple radial furrows. Deep circular groove. Margin centrifugal of this groove as broad as the central part. In every Octant 8 short, pointed velar flaps between two small ocular flaps. Arms much dichotomously branched, each with 6 or 8 thicker branches. Filaments short and numerous. Arm branches projecting far beyond the margin of the Umbrella. Size : Diameter of Umbrella, 60-80 mm. Height, 15-20 mm. (?) Locality : New Guinea. Waigan Islands. Lesson. Species. Polyrhiza orithyia. Haeckel, System der Medusen. Seite, 578. 288 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, Orinhyia incolor. Quoy et Gairnard, 1833. Voyage de 1' Astro- labe. Zoophytes. Torn IV., p. 297, pi. XXV, figs. 6-10. Salainis toreumata. Lesson, 1843. Acalephes, p. 343. Salamis toreumata. L. Agassiz, 1862. Monogr. of Acal. Contrib. to tLe Nat. H. of the U.S.A. Vol. IV, p. 159. Umbrella deep cap-shaped. The central Umbrella-disc flat and thick. Depressed in the centre with ramified radial furrows. With deep circular groove. In every Octant 8 short and truncate velar, and 2 small ocular flaps. Arms much dichotomously branched; with 8-10 larger branches. Filaments numerous and short. Longer towards the centre. Arm branches projecting beyond the Umbrella. Locality : Molucca Sea. Quoy et Gairnard. Family. Pilemidce. With no mouth, and many suction openings along the arms, without tentacles. With 4 sub-genital cavities, and with dorsal and ventral suction crisps on the arms. Genus. Toxoclytus. Pilemida) without scapulets with 8 free triangular pyramidal arms, the three broad pinnate wings of which bear simple suction crisps on their free margins, with long filaments. Species. Toxoclytus roseus. Haeckel, System der Medusen. Seite, 586. Toxoclytus roseus. L. Agassiz, 1862. Monogr. of Acal. Contrib. to the Nat. H. of the U.S.A. Rhizostoma resea. Pteynaud, 1830. Lesson. Centurie Zoologique, p. 97, pi. XXXIV. Umbrella flat hat-shaped ; in every Octant 5 or 6 velar-flaps between 2 ocular flaps (1). Arms scarcely as long as the radius of the Umbrella. The upper arm cylindrical, and about as long as the triangular prismatic lower arm. Suction crisps broad and deeply incised. BY R. VON LEXDENFELD, PH.D. 289 Colour : Pale rose-coloured Gonads ; marginal flaps and auction crisps, deep rose-coloured. Size : Not mentioned. Locality : Tropic zone of the Atlantic. Reynaud. Genus. Lychnorhiza. Pilemidae without scapulets, with 8 free triangular pyramidal aims. The wings bear on their free margin numerous thick suction crisps and filaments. Species. Lychnorhiza lucerna. Haeckel, System der Medusen. Siete, 587. Tafel, XXXIV. Umbrella flat. Every Octant with 4 large pointed oval velar, and 2 small triangular ocular flaps. Arms nearly as long as the diameter of the Umbrella. Upper arm ^ as long as the lower arm. Laterally compressed and extending below to a broad triangular shoulder-flap. Lower arm triangular pyramidal, with 2 very broad and much flapped doi-sal wings, and one smaller ventral wing. Suction crisps much flapped with numerous long, ribbon-shaped filaments. Size : Diameter of Umbrella, 120-150 mm. Height, 50-60 mm. Locality : Rio de Janeiro. Von Martens. Genus. Eupilema. Pilemidae with 8 pair of scapulets, and with free triangular pyramidal lower arms. The three wings of these bear suction crisps on their free mai'gins, but no other appendages. Without terminal bulbs. Species. Eupilema scapulare. Haeckel, System der Medusen. Seite, 590. Umbrella flat hat-shaped, with vaulted dome. In every Octant 8 pair rectangular, narrow and long truncate velar flaps. The 16 intra-circular canal nets touch the distal basis of the mouth-pillars Stem of disc cubic, narrow, not broader than the pillars. Arms 290 THE SCYPHOMEDUSiE OF THE SOUTHERN HEMISPHERE, about as long as the radius of the Umbi*ella. Scapulets of the same size and shape as the free part of the upper arm ; a little shorter than the broad lower arms. Size : Diameter of Umbrella, 150 mm. Height, 50 mm. Locality : Sunda Archipel. Sumatra. Weber. Species. Eupilema claustra. Haeckel, System der Medusen. Seite, 591. (?) Claustra Mertensii. Lesson, 1843. Acalephes, p. 379. (?) Cyanea (!) Rhizostoma. Brandt, Mem. Acad. St. Peters- burgh. " Tom. IV., p. 388, 407, tab. XXXI. Umbrella flat hat-shaped. In every Octant 6 broad tri-angular velar, and two small lancet shaped ocular flaps. The intra-circular canal net arcades are distant from the mouth-pillars as much as their own breadth. Stem of disc, cubic, double as thick as the mouth pillars, arms i | times as long as the radius of the Umbrella. Scapulets half as long as the free part of the upper arm, which is a little longer than the broad lower arm. Size : Diameter of Umbrella, 200 mm. Height, 70 mm. Locality : Marquesas Islands. Smith. Genus. Pilema. Pilemidse with 8 pair of scapulets, with free, triangular, pyra- midal, lower arms. The three wings of these bear on their free margin suction crisps, but no other appendages. At the terminal end of each arm a club-shaped or triangular bulb without suction crisps. Species. Pilema cap^nse. Haeckel, System der Medusen. Seite, 645. Cephea capensis. Quoy et Gaimard, 1824. Voyage de l'Uranie, p. 568,*pl. LXXXIV, fig 9. Rhizostoma capensis. Lesson, 1843. Acalephes, 417. Umbrella semi-spherical. In every Octant six broad semi- circular velar flaps between two pointed triangular ocular flaps. (?) BY R. VOX LENDENFELD, PH.D. 291 Upper arm about as long as the lower arm. Terminal bulb adnate, triangular, pyramidal with toothed edges, half as long as the upper arm. Size: 200-300 mm., the diameter of the Umbrella, and 80-100 mm. in height. Q) Locality : Table Bay, Cape Town. Quoy et Gairnard. Genus. Rhojnlema. Pilemidre with 8 pair of scapulets and with 8 free triangular, pyramidal lower arms. The three wings bear on their free margin between the suction crisps numerous club-shaped appendages of similar shape as the terminal bulbs. Species. Rhopilema rhopalophora. Haeckel, System der Medusen. Seite, 596. Umbrella, hat-shaped, in every Octant 16 narrow rectangular velar flaps between two short lancet-shaped ocular flaps. Scapulets as long as the free part of the upper arms, half as long as the lower arm. On the free margin of the three wings there are between the flapped suction crisps numerous triangular pyi-amidal gallert bulbs of the same shape as the larger terminal bulb of the arms. Size : Diameter of Umbrella, 100 mm. Height, 50 mm. Locality : To the East of Madagascar. Itabbe. Genus. Brachiolophus. Pilemidaj with 8 pair of scapulets and with dichotomous branched lower arms, which coalesce at their base with their lateral margins, but otherwise remain free. The coecal thick-walled Manubrium does not reach as far down as the first bifurcation of the arms. Species. Brachiolophus collaris. Haeckel, System der Medusen. Seite, 597. Umbrella semi-spherical, twice as broad as high. In every Octant 8 quadratic velar flaps between two oval ocular flaps. 292 THE SCYPHOMEDUS.E OP THE SOUTHERN HEMISPHERE, Armbush truncate, conic, extending laterally downward. Pro- jecting a good deal beyond the margin of the Umbrella. Scapulets with their upper margin in the level of the margin of the Umbrella. Size : Diameter of Umbrella, 80 mm. Height, 40 mm. Locality : Galopagas Islands. Fuchs. Genus. Stomolophus. Pilemidse, with 8 pair of scapulets and dichotomous branched lower arms ; which coalesce in the greater part of the length of their sides. Only the terminal branches remain free. The coecal thick walled Manubrium extends beyond the first bifurcation of the arms. _ . , . , . .„ . bpecies. btomolopfius fritiUaria. Haeckel, System der Medusen. Seite, 598. Tafel, XXXV. Umbrella highly vaulted ; higher than semi-spherical. In every Octant 24 stump rectangular velar flaps between two oval, pointed protruding ocular flaps. Armbush stubbed conic extended downward protruding beyond the margin of the lattei-, scarcely \ of the height of the Umbrella. Scapulets hidden in the depth of the Umbrella. Size : Breadth of Umbrella, 80 mm. Height, 60 mm. Locality : Atlantic Coast of South America. Surinam. Family. Chaunostomidce. With a single sub-genital cavity, and a mouth in the lower side of the brachial disc, with eight arms, the ventral side of which contains a deep groove. Arms branched dichotomously. Secundary and tertiary branches arranged somewhat pinnate, without mai'ginal tentacles. Genus. Psetidorhiza. With one large filament at the bifurcation of the arm. The canal system consist of 16 radial canals, and a ring canal. Centrifugally from the ring-canal we find an anostomosing net- work of canals, whilst centripetally there are between two adjacent main radial canals, 10 canals running from the ring- canal in a radial direction centripetally. BY R. VON LENDENFELD, PH.D. 293 Species. Pseudorhiza aurosa. Plate III. Yon Lendenfeld. Zoologischer Auzeiger, Nr. 116. Band V., Seite, 380. Umbrella 3 or 4 times as broad as high, with a reticulate figure on the dorsal side.- In every octant between the two long and narrow ocular flaps there are 6 velar flaps, each of which consists of three secundary flaps. Arms about as long as the diameter of the Umbrella. Colour : Umbrella colourless, with a violet reticulate figure covering the Exumbrella. Entoderm of Gastral cavity, brown. Upper part of mouth, arm-grooves, rose-coloured. Arm colourless and transparent. Frills along the margin of the grooves, and distal end of long filament richly violet. Size : Diameter of Umbrella, 400 mm. Thickness of gallert of Umbrella, 30 mm. Brachial disc, 220 mm. in diameter, and 25 mm. in thickness. Ontogenesis : The embryos are carried about in pouches sus- pended in great number from the radial canals, which run centri- petally from the ring canal. They remain there till they are fit to turn into Scyphystomas, then escape and affix themselves with the aboral pole to any free submerged surface. The Scyphystoma does not differ from other Scyphystomas. Locality : Port Phillip. Von Lendenfeld. Glenelg. Haacke. Family. Versuridae. Discomedusse without tentacles and central mouth, with a single central sub-genital porticus, and with ventral suctorial crisps of the 8 mouth arms (without dorsal suctorial crisps). Genus. Hoplorhiza. Versuridae with 8 simple, free, neither branched nor fork-shaped, mouth-arms, which do not coalesce with their lateral walls. Species. Hoplorhiza simplex. Haeckel, System der Medusen. Seite, 609. 294 THE SCYPHOMEDUSiE OF THE SOUTHERN HEMISPHERE, Umbrella flat orbicular with 48 marginal flaps (in each Octant 4 large square velar-flaps between 2 tongue-shaped projecting ocular-flaps), 8 arms quite simple, cylindrical, as long as the radius of the Umbrella. Sub-genital ostia about as broad as the distance between them. Size : Breadth of Umbrella, 50 mm. Height of Umbrella, 20 mm. Ontogenesis unknown. Locality : South Australia. Bass' Straits. Mueseum, Godeffroy. Species, JLoplorhiza punctata. Haeckel, System der Medusen. Seite, 604. Umbrella slightly vaulted with 176 marginal flaps (in each Octant 10 pair of narrow round velar flaps, between 2 small recurved ocular flaps), 8 arms quite simple, cylindrical, half as long as the radius of the Umbrella. Sub-genital-ostia 3 times as broad as the pillars. Colour : Exumbrella dark violet-brown, equally speckled with white spots. Size : Breadth of Umbrella 40 mm. Height of Umbrella, 20 mm. Ontogenesis unknown. Locality : Coast of North Australia, Arnheim's Land. T. M. Elsey. Genus. Cannorhiza. Versuridee with 8 simple, neither branched nor fork-shaped mouth- arms, which are connected with their side-margins, and form together a octagonal tube with an opening underneath. Species. Cannorhiza connexa. Haeckel, System der Medusen. Seite, 605. Umbrella flat, orbicular, with 80 marginal flaps (in each Octant 8 narrow rectangular velar flaps between 2 oval pointed ocular flaps.) Brachial tube formed by the lateral concrescing of 8 cylindrical simple mouth-arms, a little longer than the radius of the Umbrella. Above half as broad as long, below the same BY R. VON LENDENFELD, PH.D. 295 breadth. The 4 wide sub-genital ostia about as broad as the strong and free pillars between them. Brachial disk about as broad as the radius of the Umbrella. Size : Breadth of Umbrella, 80 mm. Height of Umbrella, 30 mm. Octogenesis unknown. Locality : South Pacific Ocean, near New Zealand. Smith. Genus. Versura. "Versuridoe with 8 pinnate or trichotome branched mouth-arms, the upper part of the arm continues to the under adradial main branch of the under arm as far as its distal end. Numerous club-shaped vesicles between the branchial frills. Mouth cross with 4 rays, with perradial forked suctorial crisps, without central frills. Species. Versura palmata. Haeckel, System der Medusen. Seite, 606. Umbrella quite flat, scutiform, with continuous margin, 8 slight ocular incisions, and 112 marginal flaps which coalesce (in each Octant 12 narrow, rectangular velar flaps, between 2 rudi- mentary ocular-flaps which are quite joined). Sub-genital-ostia twice as broad as the pillars between. Arms a little shorter than the radius of the Umbrella, pinnate nearly hand-shaped, flat, spread out, as long as broad. Size: Breadth of Umbrella, 60 mm. Height of Umbrella, 20 mm. Ontogenesis unknown. Locality : Sunda Sea, Java, Cherebon, Andrda. Species. Verstira pinnata. Haeckel, System der Medusen, 607. Umbi'ella, flat, orbicular, with 8 deep ocular incisions and 144 marginal flaps which coalesce, (in each Octant 16 quadratic velar flaps between two small triangular ocular flaps). Sub-genital-ostia as broad as the pillars between. Arms a little longer than the radius of the Umbrella, pinnate flat, spread out twice as long as broad. 20 29G THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE, Size : Breadth of Umbrella, 80 mm. Height of Umbrella, 3 mm. Ontogenesis unknown. Locality : Indian Ocean, near the Cocos Islands. Rabbe. Species. Versura vesicata. Haeckel, System der Medusen. Seite, 645. Umbrella flat, scutiform, with 8 deep ocular incisions, 208 coalescing marginal flaps (in each Octant 24 narrow rectangular velar flaps between 2 rudimentary ocular flaps). Sub-genital ostia half as broad as the pillars between them. Arms about as long as the radius of the Umbrella, doubly pinnate, flat, spread out as long as broad. Locality : Australia (North-west Coast. 1). Weber. Genus. Phyllorhiza. Versuridae, with 8 pinnate mouth-arms. The Pinna? are only rudimentary and appear connected by a membrane, so that the whole arm attains an extended leaf-shaped appearance. Phyllorhiza punctata. Nov. sp. Plate IV. The Umbrella is nearly semi-spherical, and about half as high as broad. The Umbrella margin bears in every Octant two sickle- shaped ocular flaps, four simple and four double flaps, all of which taper centrifugally and are truncate. These flaps consist of thick gallert and are connected by thin niernbranes. Radial furrows extend centripetally from the fissions towards the centre of the disc. The sub-genital ostia are large and oval, more than twice as broad as the pillars of the brachial disc. The brachial disc is thick and a little more than half as broad as the Umbrella, octagonal, with a canal system of its own, and thickly set on its ventral side with filaments to which the young gastrulaj-embryos adhere. The mouth-arms are § as long as the diameter of the Umbrella. Colour : Brachial disc, and stem and branches of mouth-arms and also the ground substance of the gallert of the Umbrella colourless. In the gallert of the Umbrella, close to the surface, BY R. VON LENDENFELD, PH.D. 297 are groups of "yellow cells," Zooxanthella} which give the whole a brown colour. Towards the Exumbral surface there are clouds of strongly refracting minute bodies in the gallert, which give our animal the spotted appearance, from which I have derived the specific name. The suctoi'ial crisps are bi-own. The long stalked suction naps (Peitschen filamente) are coloui-less and transparent. Size : Breadth of Umbrella, 500 mm. Thickness of Exumbrella, 50 mm. Mouth-arms, 300 mm. Filaments, 200 mm. long, and at the base 10 mm. thick. Ontogenesis : The young embryos adhere to the mother's filaments until they have nearly attained the scyphystoma stage. The ephyra is brown spotted. The young medusa goes through a complicated metamorphosis, passing through stages with 24 and 16 marginal bodies. Locality : Port Jackson. Von Lendenfeld. Family. Craynbessidce. Discomedusse, without central mouth and tentacles, with a single central sub-genital porticus and with dorsal and ventral suctorial crisps and 8 mouth-arms. Genus. Cramborhiza. Crambessidge with free strong upper arm, and strong, triangular- pyramidal under-arm, the 3 pinnate wings of which possess numerous long filaments between the corymbiated suctorial crisps. Species. Cramborhiza flagellata. Haeckel, System der Medusen. Seite, 676. Umbrella slightly vaulted, hat-shaped, with 48 marginal flaps. In each Octant 4 broad, oval, velar-flaps, between 2 small triangular ocular flaps. Exumbrella finely granulated. Ostia of the sub- gential-porticus 3 times as broad as the 4 perradial pillars between them. Arms about as long as the radius of the Umbrella. Upper arm strong, cylindrical, about as long as the triangular pyramidal under arm, the 3 broad wings have strong flapped suctorial crisps, and numerous Ions filaments. 298 THE SCYPHOMEDUSjE of the southern hemisphere, Size: Breadth of Umbrella, 80 mm. Height of Umbrella, 30 mm. Locality : Coast of Brazil, Cotingeriba. Hygon. Pernambuca. Leseur. Genus. Crambessa. Crambessidse with free strong upper-arm, and strong triangular- pyramidal under-arm, the 3 broad wings of which possess suctorial crisps without especial appendages, without terminal knots or crispless appendages at the distal-end. Species. Crambessa cricciata. Haeckel, System der Medusen. Seite, 620. Rhizostoma cruciata. Lesson, 1829. Voyage de la Coquille, Zoophyt., p. 121, pi. XL, fig. 1. (?) Ehizostoma cyanolobata. Couthouy, 1862 ; manuscript. Rhacopilus cruciatus. L. Agassiz, 1862, Monogr. Acal. Contrib., IV., p. 153. Rhacopilus cyanolobatus. L. Agassiz, 18C2. Monogr. Acal. Contrib. IV, p. 152. Umbrella semi-spherical, twice as broad as high, with 48 mar- ginal flaps. In each Octant between 2 rudimentary ocular flaps, 4 large equally sided triangular velar flaps. Exumbrella with 32 (?) deep radial furrows. Brachial disc as broad as the radius of the Umbrella. Mouth-arms 1£ times as long as the radius of the Umbrella. The upper arm short and narrow, the under arm nearly 4 times as long, surrounded by thick suctorial crisps, conic, pointed at the distal end. Colour : According to Lesson, yellowish white ; Gonads and ring canal pink. According to Couthouy, blue-white, marginal flaps dark blue, suctorial crisps and arms, carmoisin-red. Size : Breadth of Umbrella, 120-150 mm. Height of Umbrella, 50-70 mm. Ontogenesis unknown. Locality : Coast of Brazil, Island Santa Catharina. Lesson Rio de Janeiro. Couthouy. BY R. VON LENDENFELD, PH.D. 299 Species. Crambessa palmipes. Haeckel, System der Medusen. Seite, 620. Umbrella semi-spherical, twice as broad as high, with 64 marginal flaps. In each Octant 6 square truncate velar-flaps between 2 projecting oval ocular-flaps, which are half as long as the former. Exumbrella finely granulated. Arms a little shorter than the radius of the Umbrella. Under-arm triangular-pyramidal, pointed, surrounded by suctorial crisps, twice as long as the short and cylin- drical upper arms, which are connected with a thin membrane. Size : Breadth of Umbrella, 40 mm. Height of Umbrella, 20 mm. Ontogenesis unknown. Locality ; Coast of North Australia, Koch. Museum, Godeflroy. Species. Crambessa mosaica. Haeckel, System der Medusen. Seite, 622. Cephea mosaica. Quoy et Gaimard, 1827. Voyage de l'Uranie, Zoologie, p. 569, pi. 85, fig. 3. Rhizostoma mosaica. Eschschokz, 1829. System der Acalephen, p. 53. Rhizostoma mosaica. Huxley, 1849. Philosoph. Transact., 1849. pp. 422, 432, pi. 38, figs. 26, 27 ; pi. 39, figs. 28-34. Catostylus mosaicus. L. Agassiz, 1862. Monogr. Acal. Contrib. IV., p. 152 Catostylus mosaicus. Grenacher und Noll, 1876. Abhandl. Senkenberg, Ges. Bd. X., p. 38. Catostylus "Wilkessii. L. Agassiz, 1862. Monogr. Acal. Contrib. IV, p. 152. Crambessa mosaica. Von Lendenfeld, 1883. Zeitsch, f. wiss. Zool. Bd., 38. Umbrella slightly vaulted, nearly semi-spherical, 2-3 times as broad as high, with numerous narrow marginal flaps. (To 200 1 about 24 velar flaps on each Octant). Sides of the gastrogenital- cross nearly rectangular. The same breadth at the distal, and at the proximal end ; mouth-arms a little shorter than the diameter of the Umbrella. Under-arm conic, pointed below 300 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE, surrounded by thickly set suctorial crisps. 3 times as broad as the thin and short upper arm. Colour : Blue or brown, with a net of white lines on the Exumbrella ; male genital organs grey-green, ovaries deep orange- red. Size: Breadth of Umbrella, 200-350 mm. Height of Umbrella, 80-120 mm. Ontogenesis unknown. Locality : East coast of Australia, Port Jackson, Quoy et Gaimard, Huxley ; Illawarra Lake, T. Drayton ; Port Phillip, Port Jackson, von Lendenfeld. Genus. Mastigias. Crambessidse, with free strong upper-arms and with strong three-cornered pyramidal under-arms, the 3 wings of which have suctorial crisps. At the distal end of each arm there is a club- shaped, mostly three-cornered, gallert appendage (or terminal knot), without suctorial crisps. Genus. Mastigias papua. Haeckel, System der Medusen. Seite, 123. Mastiguas papua. L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 152. Cephea papua. Lesson, 1829. Voyage de la Coquille Zoophyt., p. 122, pi. XL, figs. 2, 3. Cephea papuensis. Griffiths, 1832. In Cuvier's Anim. Kingd., pi. III., fig. 3. Cephea ocellata? Huxley — (non Peron !) — 1877. Manual Invert. Anim., p. 137, figs. 19, 21. Bhizostoma papua. Lesson, 1843. Acalephes, p. 715. Umbrella semi-spherical, with 8 marginal flaps (in each octant 8 semi-circular velar flaps between 2 narrower ocular flaps.) Arms (without appendix) about half as long as the radius of the Umbrella. Upper arm and under arm nearly the same length. Terminal appendix three-cornered prismatic, a little longer than the diameter of the Umbrella. BY R. VON LENDENFELD, PH.D. 301 Colour : Exumbrella bluish green to brownish green, some times more blue or more green, or more brown, with numerous large white spots. Subumbrella light brown, with 8 blue or bluish green ocular canals. Marginal flaps and Gonads rust-colour, brown, blue-green, with brown spots and suctorial crisps. Terminal appendage blue or green- towards the end reddish brown. Size ; Breadth of Umbrella, 60-80 mm. Height of Umbrella, 30-40 mm. Locality : New Guinea (Waigon and Dorey), Lesson ; Louisiade- Archipelago, Huxley ; Philippines, Wendt ; China Sea. H. Koch. Species. Mastigias ocellata. Haeckel, System der Medusen. Seite, 623. Medusa ocellata, Modeer, 1791. Nova. Acta. phys. med. n.l., VIII, Apend., p. 27, nr. 11. Cephea ocellata, Peron et Leseur, 1809. Tableau des Meduses, etc., p. 361, nr. 98. Cephea ocellata, Eschscholtz, 1829. System der Acalephen, p. 56. Cephea ocellata, L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 156. Hidriticus rufus, L. Agassiz, 1862. Monogr. Acal. Contrib., IV., p. 158. Umbrella semi-spherical, with 112 marginal flaps (in each Octant 12 truncate, rounded velar flaps between 2 oval projecting ocular flaps.) Arms (without appendage) shorter than the radius of the Umbrella. Upper arms a little longer than the shortened broad under arm. Terminal appendage, club-like, three-cornered, as long as the radius of the Umbrella. Colour : Exumbrella bright reddish, with numerous white, spots surrounded by brown. Margin of Umbrella and Gonads darker red. Arms reddish with small white papillae, Terminal appendage transparent at the end with a blue stripe. 302 THE SCYPHOMEDUSJE OF THE SOUTHERN HEMISPHERE, Size : Breadth of Umbrella, 50-60 mm. Height of Umbrella, 20-30 mm. Locality : East part of the Indian Ocean, near the Cocos Islands, Rabbe ; Sunda Straits, W. W. Wood. Species. Mastigias pantherina. Haeckel, System der Medusen. Seite, 624. Umbrella semi-spherical, with 144 marginal flaps (in each Octant 1 6 narrow rectangular truncate velar flaps, between 2 small lancet-shaped ocular flaps. Arms (without appendage), nearly twice as long as the radius of the Umbrella. The upper arm scarcely as long as the slender three-cornered pyramidal under- arms. Terminal appendage three-cornered prismatic, very thin and long, filiform, 2-3 times as long as the diameter of the Umbrella. Colour : Exumbrella (in spirits of wine), dark brown, with numerous and large white spots, which are surrounded by a broad black border. Size : Breadth of Umbrella, 50-60 mm. Height of Umbrella, 20-30 mm. Locality : Tropic Pacific Ocean, Samoa Islands, Museum. Godeffroy. Genus. Eucrambessa. Crambessidse with free strong upper arm, and strong three- cornered pyramidal under arm, the 3 wings of which possess numerous clublike appendages without frills. Appendages of the suctorial crisps, of the same shape as the terminal gallert knots. Species. Eucrambessa Mulleri. Haeckel, System der Medusen. Seite, 624. Umbrella slightly vaulted, 3 times as broad as high, with 80 marginal flaps (in each Octant 8 large quadratic velar flaps between 2 small three-cornered ocular flaps.) Arms about as long as the BY R. VON LENDENFELD, PH.D. 303 diameter of the Umbrella, between the suctoral crisps of their wings there are numerous three-cornered gallert clubs, of the same shape as the larger terminal knot of each arm. Size : Breadth of Umbrella, 120 mm. Height of Umbrella, 40 mm. Locality : Indian Ocean, Madagascar. Levasseur. Genus. Thysanostoma. Crambessidse with weak, shortened and mostly coalescent upper arm, and strap-shaped, very elongated, three-cornei'ed, prismatic under arm, the three narrow wings possess suctorial crisps in their whole length, without terminal knot. Species. Thysanostoma thysanura. Haeckel, System der Medusen. Seite, 625. Umbrella nearly orbicular, 2-3 times as broad as high with 96 marginal flaps (in each Octant 10 truncate rounded velar flaps between two pointed three-cornered ocular flaps.) Exumbrella polygonal, slabbed with irregular and granulated slabs, which are scarcely half as broad as the marginal flaps. Sub-genital ostia 4-6 times as bi'oad as the pillars. Arms 2-3 times as long as the diameter of the Umbrella, very narrow, ribbon shaped, thi*ee- winged, the same breadth nearly throughout their whole length to the rounded end. Size : Breadth of Umbrella, 8 mm. Height of Umbrella, 3 mm. Locality : Australia, Museum. Godeffroy. Species. Thysanostoma melitea. Haeckel, System der Medusen. Seite, 626 Melitea brachyura. Lesson, 1830. Centurie Zoologique, p. 227, pi. 80. Rhizostoma brachyura. Lesson, 1829, Voyage de la Coquille, Zoopht., Tom. II., p. 120. %AA 304 THE SCYPHOMEDUS^E OF THE SOUTHERN HEMISPHERE, Thysanostoma Lessoni. L. Agassiz, 1862. Mongr. Acal. Contrib. IV., p. 153. Umbrella semi-spherical, twice as broad as high, with 80 (?) marginal flaps (in each Octant 8 rectangular flaps, the sides of which coalesce. The velar flaps are truncate and lie between two elon- gated ocular flaps.) Exumbrella prettily and regularly slabbed with polygonal (5 or 6 cornered) slabs, which are as broad as the marginal flaps. Arms several times as long as tbe diameter of the Umbrella, very thin, getting gradually thinner towards the pointed end. Colour : Umbrella whitish, with rust-coloured margin, Gonads yellowish, arms dark yellowish-red. Size : Breadth of Umbrella, 300-400 mm. Height of Umbrella, 100-200 mm. Locality : New Guinea, Harbour of Dorey. Lesson. Genus. Leptobrachia. Crambessidse without free uppei'-arms, with ribbon-shaped, very long and thin under arms, which possess suctorial crisps towai-ds the distal end above the terminal knot. Mouth-cross with 4 rays with- out special frills. Species. Leptobrachia le])toptts. Haeckel, System der Medusen. Seite, 630. Leptobrachia leptopus. Brandt, 1838. Bulletin Acad. Petersb., Tom. I., Nr. 24, p. 191. Leptobrachia leptopus. L. Agassiz, 1862. Monogr. Acal( Contrib., IV., p. 154. Rhizostoma leptopus. Chamisso et Eysenhardt, 1821. Nova, Acta phys. med. n. e., Tom. X.. p. 356. Taf., 27. Rhizostoma leptopus. Eschscholtz, 1829 System der Acale- phen, p. 52. BY R. VON LENDENFELD, PH.D. 305 Rhizostonia leptocephalus. De Blainville, 1834. Actinologie, p. 298. Umbrella semi-spherical, with 48 marginal flaps. In each Octant 4 rectangular velar flaps between 2 small ocular flaps (?). Subgenital ostia twice as broad as the pillars between ; the mouth cross smooth. Arms very long and thin, ribbon-shaped, about twice as long as the diameter of the Umbrella, with a bundle of frills, at the end from which there protrudes a pointed terminal knot. Colour : Pale violet ; marginal flaps, margin of the arms and terminal suctorial crisps, dark violet ; Gonads, yellow. Size : Breadth of Umbrella, 8 mm. Height of Umbrella, 40 mm. Locality ; Tropics of the Pacific Ocean, Radack Island. Chamisso. Genus. Leonura. Crambessidse without free upper arms, with ribbon-shaped, very long and slender under-arms which only have suctorial crisps towards the distal end above the terminal knot, mouth cross with 8 rays and 8 adradial suctorial crisps, which form especial frills round the centre of the brachial disc. Species. Leonura leptura. Haeckel, System der Medusen. Seite, 631. Umbrella flat, oi'bicular, with 80 marginal flaps. In each Octant 8 rectangular velar flaps, between 2 pointed triangular ocular flaps. Sub-genital-ostia 3 times as broad as the pillars between them. Mouth cross of the brachial disc with frills ; the 8 rays in pairs. Arms very long and slender, ribbon-shaped, nearly three times as long as the diameter of the Umbrella, a bundle of frills, at the end which surrounds a pointed three-cornered terminal knot. Size : Breadth of Umbrella, 100 mm. Height of Umbrella, 50 mm. Locality : South Pacific Ocean, near New Zealand. Weber. 306 THE SCYPHOMEDUS.E OF THE SOUTHERN HEMISPHERE. Species. Leonura terminalis. Haeckel, System der Medusen. Seite, 696. Umbrella slightly vaulted with 80 marginal flaps. In each Octant 8 pointed 3-cornered velar flaps between 2 small divergent ocular flaps. Sub-genital-ostia 3 times as broad as the pillars between. Mouth cross of the brachial disc with regular frill with 8 rays. Arms not very long, ribbon-shaped, about as long as the diameter of the Umbrella, with a tassel-shaped bundle of frills, which surround a 3-cornered, projecting terminal knot. Size ; Breadth of Umbrella, 80 mm. Height of Umbrella, 20 mm. Locality ; Pacific Ocean, " Challenger " Expedition. "Wy ville Thomson. Explanation of Plates. Plate III. — Pseudorhiza aurosa, von Lendenfeld, painted from life, 0*5 natural size. Plate IV. — Phyllorhiza punctata, von Lendenfeld, painted from life, 0 5 natural size. NOTE ON THE DEVELOPMENT OF THE VERSURID^E. Plate V. By E. Vox Lendenfeld, Ph.D. Although the early stages of development, the Gastrula and Scyphistoma of some of those Phizostomse which possess a single Sub-genital space, the Monodenmia of Haeckel, are known of one or two species ; the later stages, the Ephyra and the Metamorphosis of these Medusas is unknown. Only Haeckel observed young stages of a Medusa belonging to the Crambessidae, but these also had attained a size of from 30 to 40 mm., and appeared similar to the adult animal. (1.) I have had the luck to capture some very young stages of the Phyllorhiza punctata, a new species described in another paper (2), which is very abundant in Port Jackson. The smallest of these measured 15 mm. across the disk, and I obtained an unlimited number of specimens from this size upward to the adult animal, which measures half a meter across the Umbrella. In colour and shape these small larvse are similar to the adult animals. Claus (1) has described the development of the Mouth-arms in Rhizostoma Cuvieri (Pilema pulmo. Haeckel), which belongs to the Family Torenmidse. In our species the Mouth-arms follow in their development a similar course as that described by Claus. The Sub-genital space appears to be formed in the way that Haeckel supposes, but I am as yet not quite sure on this point. (1.) Since this paper was read I received " Untersuchungen tiber die Organisation und Entwiclcelung der Medusen." By G. Claus, in which paper the Metamorphosis of Catylorhiza tuberculata is described (page 43, f. f.) The characteristic peculiarity in the Metamorphosis of Phyllorhiza punctata — the decrease of the number of marginal bodies does not occur in Cotylorhiza. The cause of the brown colour in the latter is ascribed by Claus to Zooxanthellae in a similar manner as by myself in Phyllorhiza. (2.) Proc. Lin. Soc. N.S.W., Vol., IX., p. 296. 308 NOTE ON THE DEVELOPMENT OF THE VERSURID^E, The number of marginal bodies or organs of sense (Sinneskolben) is in the Discomedusse nearly always eight, only very few possess more, none less. The number hardly ever exceeds 32. The develop- ment of the forms with more than eight marginal bodies is unknown. Haeckel (1) supposes that in these cases already the Scyphystoma possesses a greater number of tentacles. Our Phyllorhiza, in its adult state possesses eight marginal bodies, between every two of which there are two ocular flaps, four simple and four double marginal flaps (plate V., fig. 4.) I have never observed any variation in the number of the marginal bodies of the adult animal except when the margin had been injured, in which case, marginal bodies are produced irregu- larly in the regenerated and irregular part of the margin. The young stages (plate V., figs. 1-3) possess a greater number of marginal bodies. It is not likely that Phyllorhiza punctata will differ in this respect from all the other members of the Family, and so we may assume it as not unlikely, that the development described below for Phyllorhiza punctata is met with in many of the other Versuridse. The youngest stage which I have observed, measuring 15 mm. (fig. 1) possesses 24 marginal bodies. In the radii of the first, second, and fourth order. The margin of the Umbrella bears in each Octant between two ocular flaps, four broad and low ^flaps which are to be considered as two flaps only, each possesses an indenture in the middle, the accessary marginal bodies are situated in these indentures. These sense-oi-gans are slightly smaller than the persisting eight, but do not differ from them in shape. Larvse measuring 30 mm. across the Umbrella show these marginal bodies in a few Octants only, whilst in the others there is situated only one sense-organ in the Radius of the third order. It is evident that the larva? lose these marginal bodies of the quarternary Radii at the time of their attaining this size. They are slowly replaced by others, one always taking the place of two. A form is in that way attained, (1.) E. llaeclul. Das System der Medusen. Seite 45S. BY R. VON LENDENFELD, PH.D. 309 which possesses eight accessory marginal bodies besides the eight persistent ones. (Fig. 2.) The flaps of the Umbrella margin adjacent to these ad radial marginal bodies grow out to greater length and commence to divide into two flaps by fission. Larvae, with a diameter of 50 mm., loose these adradial bodies also (fig 3), and by a continued fission of the maginal flaps the configuration of the Umbrella margin of the adult animal is attained. Such a formation of marginal bodies has, to my knowledge, not been observed before, and tends to prove the great fundamental difference between these Scyphomedusse which have more marginal bodies in the young than in the adult state, and Hydromedusse, which often possess fewer sense-organs, when young, than when grown up. Explanation of Plate. Plate V.— Part of the Umbrella margin of Phyllorhiza punctata, all enlarged so as to be of the same size. Fig. 1. Larva with 15 mm. diameter. Fig. 2. Larva with 30 mm. diameter. Fig. 3. Larva with 50 mm. diameter. Fig. 4. Adult with 250 mm. diameter. 310 A MONOGRAPH OF THE AUSTRALIAN SPONGES, A MONOGRAPH OF THE AUSTRALIAN SPONGES. By Dr. R. von Lendexfeld. II. — Continued. MORPHOLOGY AND PHYSIOLOGY OF THE SPONGES. I will endeavour to give a brief account of our present know- ledge on the subject, without entering into detail, which will be described below in the classificatory portion of this work. I. — The Anatomy of the Sponges. 1. Shape and size. Although many Sponges have a constant shape, which is characteristic for the species, still the greater number do not possess a definite form. The same species will always be charac- teristic in outer appearance, but a certain shape which could be minutely described and set up for a standard is not met with in most Sponges. Just as a tree although growing irregularly, will have peculiar points about it, which give the character to the landscape so it is with the Sponges. The irregular Sponges appear in every conceivable shape. Those which have a constant shape are generally cylindrical, always with a circular transverse section, which points to the fact that we have here animals before us, which originally irregular, are just commencing to attain a regular radially sym- metrical shape, or vice versa. The latter appears more probable. BY R. VON LENDENFELD, PH.D. 311 In detail the form of a species is very constant, so that Sponges from the same locality growing in the same depth, and under similar outer circumstances, will always at first sight prove their identity, may their shape differ ever so much. The configuration of the surface, the height of the projecting conuli, and their distance from each other, and the size of the Oscula are alike. Also, the structure of the skeleton is much more constant than the shape. The more we go into detail the more constant peculiarities are met with, so that the microscopic investigation will often prove two specimens to be identical, which are very different in shape. The size is subjected even to greater variations than the form. Many Sponges certainly do not grow beyond a certain limit, bat there are others which grow indefinitely — that is all those forms, which are found in the shape of incrustations. Spongecrusts may extend for miles. The margins of different crusts coalescing, and finally covering the whole of the area in which the Sponge in the struggle for life has the upper hand. Such a Sponge is for instance our Aplysilla violacea (1) which covers many thousand square meters in Port Phillip. In such cases it is difficult to say what should be considered as an individual. Whilst the Sponges with characteristic shape can be easily recognised either as single persons or as colonies of such, whereby all individuals are alike and moi'e or less separate, these unlimited sponges can only be understood asZoa Impersonalia (Oscar Scmidt.) Together with the characteristic and constant shape we find the individuality of the Sponge slowly disappearing, whereby not cleaiiy personified individuals are derived from personified species of definite shape. This certainly tends to prove that these inde- finite Sponges are not to be confounded with higher indivi- dualized Coelenterata, but we must always bear in mind, that they pass an embryonic stage, which is of characteristic, constant and (1) R. von Lendenfeld. Ueber Goelenteraten der Siidsee II. Ntue -Apty- siniJ.a. Zeitschrift fiir wissenschaftliche Zoologic. Band, XXXVIII. 21 312 A MONOGRAPH OF THE AUSTRALIAN SPONGES, definite shape, so that the loss of individuality which occurs later is not the original, but only a coenogenetic peculiarity. The largest Sponge of definite shape and attaining a height of one metre or more is Poterion. 2. The color. In many Sponges the color is less variable than shape and size, even in the indefinitely shaped species it never varies near as much as often in higher animals. I consider the colour in life as a very constant and characteristic feature, so much so, that I would always be inclined to consider a Sponge as belonging to another species ; when the color differs though otherwise similar in shape and structure. Unfortunately the colour is very delicate and always fades in spirits or changes even totally in a few minutes. The outer sui-face is mostly monochromatic, although it happens sometimes that one part of a Sponge is lighter than another. &pots or figures of any kind never occur in the surface color. Sponges may have all colors except green. (Spongilla sometimes contains chlorophyll and then appears green.) When the colour is not uniform then the lower side is always lighter than the upper, as in fishes. This appears to be less of a protective arrangement than a consecpience of the photographic effect of the light, which causes the exposed surfaces of the Sponge to attain a darker hue than those which are always in shade. If the colour of the Sponge is not uniform then the lighter part is always the same tint as the darker, only a lighter shade. We have here apparently the same difference as between the colours of the soles and palms and the other part of the skin of dark human tribes. Deep sea Sponges are always colorless. The Calcareous Sponges are white or light yellow, the Horn- sponges always richly coloured, yellow, orange, blue, red or violet; the Siliceous Sponges, with the exception of those from great depths (Hexactinellidpe and Lithistida?) also appear coloured, but not so intensely as the Ceraospongia?. The interior of the Sponge is mostly of a similar hue as the surface but always more dull. BY R. VON LEXDEXFELD, PH.D. 313 The color may be diffuse, but is also often exclusively found in granules which may be imbedded in the gallert or in the cells of the Sponge. Of the changes which the colours of Sponges undergo when dying, those are most remarkable, which are met with in the yellow Aplysinidaa and Apjysillidse, they turn dark blue. 3. Internal structure. The skin or outermost layer of the Sponge is often only loosely connected with the main part of the body, and can be removed from the concave fields between the conuli. The body appears on a transverse section, more or less porous. The pores are the orifices of the channels which traverse the body of the Sponge in every direction. The lumen of these canals varies very much so that in some cases the Sponge appears very porous, only about 30% of the space being taken up by the Sponge substance itself, whilst all the rest is canals. In other cases again the canals become rare and narrow and are often quite invisible. This, for instance, often occurs, when a living Sponge is cut, because the whole of the body contracts so much that all the vacant space is filled up by the Sponge tissue and all the water ejected. Also the hardness is subject to great variations. Some Sponges, without skeleton, appear very soft, nearly slimy ; whilst others again, particularly the Lithistida?, attain the hardness of a stone. But not only does the skeleton make a difference in this respect, the ground substance of the Sponge itself varies greatly in its density between the slimy appearance of a soft gallert and the resistent form of cartilage. 4. The Canal-system. The canals are mostly crooked and irregular, only in a few Sponges they appear, as more or less, parallel and straight tubes. Their breadth varies very much, although it often happens that they will all appear of the same width in a section. From the 314 A MONOGRAPH OF THE AUSTRALIAN SPONGES, microscopic pores of the surface the water either enters cavities which lie underneath the skin, the subdermal cavities (Carter) or flows through small canals which join and form larger tubes. These tubes afterwards again give rise to smaller ones, which by- continual ramification finally supply the greater part of the whole Sponge. In no part of the Sponge this system of canals, through which the water flows centripetally, is in direct connection with those canals through which the water passes on to the oscular tube. There is always a layer of ciliated chambers present in the Sponge, which layer separates the ectodermal canal system which brings the water to the ciliated chambers, from the canal system which carries the water away from the chambers to the oscular tube, these latter canals are coated with Entoderm. The layer of ciliated chambers is mostly folded in a very complicated manner. Originally it has always been of a simple sack-shape, from which shape the complicated structure of the adult Sponge is derived. (F. E. Schulze Plakinidse.) The Ectodermal water-supplying canals are to be compared with trees which grow from the sub-dermal cavities or corresponding parts. Also, the Entodermal drain-channels are tree-shaped. The narrow canals arising from the ciliated chambers unite to form larger branches which again, like tributary streams, run together, uniting to a main drain which opens into the oscular tube or cloaca. Only in a few Sponges, particularly the Syconidee, the canal system is simple and unbranched. The Asconida? (Leucosolenia) possess no canal system. All the mains open into a tube very much wider than any of the others, which stands vertical on the surface of the Sponge. This Oscular tube is mostly very wide, always when expanded visible to the naked eye. It can be compressed, and may under circumstances be quite oblitered if the Sponge contracts very much. (Lipostomie.) This Oscular tube opens on the surface of the Sponge, with a simple, circular aperture. In the case of the Sponge being cylindrical, or consisting of a lot of parallel cylinders, there is nearly always an Osculum or opening of the Cloaca at the terminal face of every cylinder. Complications of this simple BY R. VON LENDENFELD, PH.D. 315 form of Osculum may arise, by a net-work being formed which closes the wide Osculum (Euplectella). Sometimes a thin chimney- shaped membrane projects from the Osculum. (Caminus.) Sometimes a frill of large spicules surrounds the opening (many Calcareous Sponges, Holtenia.) The tube itself may possess transverse membranes, which by being more or less tightened regulate the current of water (some Spongidse). 5. The Skeleton. By far the greater portion of known Sponges possess a skeleton, which in its shape and size is as variable as the shape of the Sponge itself, but which in its minute structure appears rather unvarying. The daughters may have a very different skeleton from the mother as far as shape and size, probably also as far as sti-ength is concerned ; but the minute structure will resemble that of the parent so closely, that we are justified in looking on the minute structure of the skeleton as a very important feature of the Sponges in as much as their mutual relationship is concerned. Some Sponges — and as we may safely assume, those resembliug the ancestral forms — have no skeleton. One or several of such ancestral soft forms attained a skeleton, consisting of carbonate of lime (Calcarea.) Others again produced fibres, which were originally composed of fibrillous tissue only (GumminaB.) In the course of time horny fibres were produced in the centre of the fibrellous fibres, and these of course followed the direction of the large canals (Oscar Schmidt). Originally they had a tree-shape (Aphysillidae, von Lendenfeld, Vosmaer.) The branches coalesced, and a reticulate structure was produced, in which main centrifugal stems could be distinguished from tangental connecting fibres (Spongidse, Aplysinida?. ) Foreign bodies, sand and the like, adhering to the surface of the Sponge, in most cases entered the horny fibres and filled t" e core of them in a varying degree. Such foreign bodies ar mostly only to be found in the radial fibres, but sometimes ? oin the tangental ones. 316 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Within these horny fibres sometimes cells are to be found, which like the Osteoklasts of the vertebrate animals destroy the hard substance, here the Spongiolin or horn, and cause the skeleton to appear as a system of tubes filled with a soft core. (Aplysillidse, von Lendenfeld.) It is perhaps possible that these cells are Algfe symbyotic in the Sponge. Silicious spicules may be formed within the horny fibres, and these always belong to the Monactinellid type, a rod with one or two points. They are small in number and size at the beginning (Veluspa, Miklouho-Maclay), but get larger and more numerous until the horny fibres are nearly entirely replaced by dense bundles consisting of Monactinellid spicules only. At the same time in all of the stages from a soft non-skeletous Sponge (Halisarca), to a Sponge with a strong skeleton of silica- cords (Suberites), silicious spicules may be produced outside the fibres in the ground substance of the Sponge. These iiever belong to the Monactinellid type. They are always originally charac- terized by possessing more than two ends — more than one axis. These " flesh spicules " attain very extraordinary shapes. If they appear in Sponges, which already possess a strong fibrous skeleton, they remain small and loose (Desniacidonidas, O. Schmidt) ; if on the other hand they make their appearance in Sponges which are destitute of a fibrous skeleton they attain a larger size and coalesce to form a hard, continuous skeleton (Hexactinellidse, Tetractinellida?, Lithisticlre. Monactipyalea.) Originally these spicules were small and scattered. Such ancestral forms were probably allied to the Plakinidas (F. E. Schulze) ; or to those Chondrosida?, which possess silicious bodies in their outer layer. The Sponges are therefore, as far as the skeleton is concerned, to be grouped along two divergent directions, both of which take their origin in the Sponges without a skeleton. The one row comprises the calcareous, the other the horny and silicous Sponges. (Grant, Vosma^r.) The latter group appears as a straight row (stem) culminating in those fibrous Sponges, in which all the horny substance has been replaced by Monactinellid silicous spicules, and comprising the horny Sponges, Ceraospongige (0. BY R. VON LEXDENFELD, PH.D. 317 Schmidt), and Monoctinellidae (Zittel.) From the whole extension of this line or stem, branches take their origin, which are parallel to one another and run in the same direction. Large at the bottom, these branches taper towards the top ; they include the Desrnacidonidae (small branch near the top.) Plakinidre, Tetractinellidae, Lithistidse and the Hexactinellidre, two large branches at the bottom, and some Sponges which ai'e allied to the Ceraospongise, near the middle of the stem, but nevertheless possesses flesh spicules. (Das System der Monactinella?, von Lendenfeld and elsewhere.) We will return to this subject further on, under the heading " Classification." II. — The minute structure of Sponges. As eveiy other Metazoan, the Sponge consists of a great many cells, different in form and function ; and the products of these cells. It appears cpiite logical to call the Sponge a colony of Protozoa, but it must be borne in mind that every other Metazoan is just as much a colony of Protozoa, as the Sponge. The latter view is generally accepted, only that we do not call higher animals colonies of Protozoa. The mass of the Sponge consists, like the Umbrella of the large Medusae of connective tissue (Binclegewebe)1 which may be of a more gallerty or a more cartilage-like texture. It is to be compared to the tissue which forms the umbilical cord known as Wharton's galiert. This ground substance is in many cases without visible structure, in others again it attains the characters of fibrous tissue, and then the whole Sponge accordingly has a tenacity like leather (Chondrosia.) In this ground substance we meet with cells and all the surfaces of it are covered with Epithelia, so that the ground substance comes in contact with the surrounding water nowhere. These Epithelia are of a simple structure, and consist of one layer of cells only. The muscular fibres are not in connection with Epithelial cells, but produced from cells imbedded originally in 318 A MONOGRAPH OF THE AUSTRALIAN SPONGES, the gallert, so that the main cause of the formation of a Sub- epithelial layer in other Coelenterata does not influence the Sponges. And as there also do not seem to be any nervous elements in tbe Epithelia of the Sponge, no reason exists why a Sub-epithelial layer should be formed. (The origin of the Sub- epithelial layer in other Coelenterata ; compare O. and R. Hertwig, Das Nervensystem und die Sinnesorgane der Medusen.) The ground substance, together with the cells imbedded therein, is to be considered as Mesoderm, whilst the Epithelia are partly Ectodermal and partly Entodermal. We shall commence with the description of the Ectoderm. 1. Ectoderm. The whole outer free surface of the Sponge is covered with a low Epithelium, consisting of flat covering cells, each of which may possess one swinging cilia. The tubes which connect the outer surface with the inner canal system direct, or with the subdermal cavities are covered by a continuation of the Ectodermal Epi- thelium of the outer surface. The subdermal cavities and the canals leading from them to the ciliated chambers are also covered with the same Epithelium. Here the Ectoderm ends and all other surfaces of the Sponge are covered with Entoderm. (F. E. Schulze. Plakinidas.) According to the interesting observations of Marshall, it does not appear improbable, that the Epithelium on the surface also of those canals through which the water flows towards the ciliated chambers is to be considered as Entoderm. In Reniera filigrana the parts of these canals adjacent to the ciliated chambers certainly are covered with Entoderm. But Marshall shows also in an extremely ingenious manner, that in those cases where these canals are originally rarely formed by the Ectoderm, they may be considered as Entodermal structures, because they are formed by an invagination, which takes place very early, and may therefore be considered as a sort of Gastrular invagination. BY R. VON LENDENFELD, PH.D. 319 "Whether numerous invaginations as those which according to F. E. Schulze form these canals, ought to be compared to the invagination of the Gastrula, it is here not the place to discuss, but if we followed this custom throughout, we would have to call the sweat glands in our skin also Entodermal, because they are produced by an invagination of the Ectoderm. I think that an invagination of Ectoderm can never produce an Entoderm, but that an Entoderm can only be produced from an indifferent Blastula which does not consist of Ectoderm. In the case of the Sponge Embryo the outer surface is covered by Ecto- derm, and the invaginations take place after the Entoderm has been formed. The statement of Marshall, that the canals taking their origin between the Entodermal ciliated chamber, and the Ectodermal surface layer, by these two layers moving away from each other, after they have grown together (Plakina), may be formed as likely from the ciliated chambers as from the Ectodermal surface, appears indisputable ; and I gladly accept it, because the digestive func- tions which I ascribe to the Epithel of these canals and the sub- dermal cavity, perhaps also point to an Entodermal origin of those cells. 2. Entoderm. Whilst the Ectodermal cells, although performing manifold duties, are apparently (only few Sponges have been investigated with sufficient care) of a uniform shape, the Entodermal Epithelia are different in the different parts of the Sponge. In the ciliated chambers they are elongate, cylindrical, and contain a Protoplasma which imbibes colors very freely ; in the canals leading from the chambers to the oscular tube, and on the surface of the latter they resemble the Ectodermal cover cells, although they never appear quite so low as these (Aplysillidse, von Lendenfeld). The ciliated chambers in the Calcispongise often have the shape of long tubes (Radial tubes Syconid?e). In all other Sponges they are pear- shaped, sometimes elongated and sometimes nearly spherical They vary very much in size. (Sack-Birn-Halb.-Kugel fbrniig, F. E. Schulze). 320 A MONOGRAPH OF THE AUSTRALIAN SPONGES, These ciliated chambers are the main characteristic of the Sponges and have no homologue in other Coelenterata. The cells which cover the inner surface of the chambers, always possess a frill at their free end, and a cilia in the middle of the free surface. Standing close together, and pressing each other laterally, they attain the shape of hexagonal prisms. At the vaulted end of the chamber a few of these cells here and there are wanting ; here the pores are situated, through which the water enters the chambers from the supplying Ectodermal canals. These apertures are always very small, and it appears that the Sponge has the power of closing some or all of them. Towards the other end of the chamber the cells get gradually lower and pass into the Entodermal Epithel of the drainage canals. There always is only one outlet, and this is of a large size, generally about half as wide as the chamber itself. It cannot be closed by the Sponge. The Entoderm covers the surfaces of all the drainage-canals, and the oscular tube and ends at the margin of the latter. The boundary between Ectoderm and Entoderm lies in the circum- ference of the Osculum. 3. Mesoderm. The same difference between the structure of the Mesoderm of the Polypomedusa? on the one hand and the Ctenophorse on the other, (Hertwig der Bau der Ctenophoi-en, Chun die Ctenophoren des Golfes von Neapel), also appertains between the Mesoderm of Polypomedusse and the Mesoderm of Sponges. In some respects the Sponge mesoderm shows affinities to the Mesoderm of the Ctenophorse. Whilst the cells in the ground substance of the Polypouiedusfe, that is the primary Mesoderm, (von Lendenfeld : Encopella campanularia) have only a nourishing function and are derived from the Entoderm ; the Mesoderm cells of the Ctenophorfo and Sponges have other functions also, and are in the Ctenophorte (Kawolevsky) and, perhaps, also in the Sponges derived from the Ectoderm. BY R. VON LENDENFELD, PH.D. 321 If we compare the Histology of the Sponges, Pol yponiedusse, Actiniaria, and Ctenophora?, we shall find that the four groups differ from each other in the following manner : — The principal oi'gans in the Ectodermal Epithel, Polypomedusse. The principal organs in the Entodermal Epithel, Actiniaria. The principal — or many. — organs in the primary Mesoderm or ground substance, Sponges and Ctenophorae. As mentioned above, the ground substance, which is a product or secretion of the Meso-dermal cells, mostly has the appearance of structureless gallerts, or harder substance, which in every case contains a large proportion of water. The minute fibrelles found in it run in every direction and are often dense and wavy so as to resemblance for instance the connective tissue in the cervical teidon of a bullock. Cells of the Mesoderm. The numerous cells of the Mesoderm have very different shapes. They possess a spherical or oval nucleus around which the Protoplasm is amassed. These cells are destitute of a cell- wall. From the central mass of Protoplasme prolongations extend exceeding in length the diameter of the central part manifold. These processes are not numerous 2-6. The most indifferent forms have processes which may extend in every direction. With a higher development of these elements their processes get fewer in number, and extending along one plane only. In the case of only two such excrescences being developed, they always lie at opposite ends of the cell and in one line — here we have arrived at a form of Mesodermal cell, which is to be termed a musular cell. Near the surface of the Sponge in the membrane which divides the Sub-dermal cavities from the outer water these cells have their prolongations extended in a tangental plain, they are mostly two in number but sometimes also three are met with. Around the canals and the Oscular tube we often find these cells in dense masses, and their prolongations mostly running parallel to the adjacent surface. The extensive movements of the outer skiu and the canals is doubtlessly the result of the contraction of the processes of these cells. The interesting fact of their being 322 A MONOGRAPH OF THE AUSTRALIAN SPONGES, sometimes, particularly in the skin, such cells with three processes, show a mode of the formation of muscular tissue, very different from that known in the other Ccelenterata in detail, but still essentially the same, (von Lendenfeld neue Aplysinidse, Kleinen- bei'g Hydra.) A tube consisting of a dense mass of such Mesodermal cells covers in some Sponges the fibres of the skeleton. These cannot be considered as muscular, but rather as a sort of tissue like the periost. Another interesting and much more differentiated form of Mesodermal cells are large gland-cells, which invest the growing horn-fibres of Ceraospongiae and secrete the horn substance. (F. E. Schulze, Spongidse). Similar cells are met with along the outer surface of the sponge. These produce a slime which protects the Sponges from noxious influences from without. (Merejkovsky, Eponges de la mer blanche, von Lendenfeld neue Aplysinidae.) These cells have the shape of round balls of Protoplasm, investing the spherical nucleus from which threads of Protoplasm 3-10 in number take their origin, and remaining parallel with each other connect the body of the cell with the surface where the secretion is to be poured forth. These threads are as long or longer than the main body of the cell and stand vertical on the surface of secretion. Cells in the core of the hollow-fibred Sponges, which act like the Osteaklasts, and produce the pith in the fibres of the Sponges, are also derived from the Mesoderm. (von Lendenfeld das Hornfaserwachsthum der Aplysiuidse.) (1) It appears from this that the skeleton of the Ceraspongiai is a Mesodermal structure. The cells in the Protoplasm in which the calcareous and silieious spicules take their origin, also belong to the Mesodermal layer, and are of an indifferent shape. We now Lave to review a series of Mesodermal elements, which are alike in shape at certain stages of their development, but which perform very different functions. (1.) Possibly symbiotic Algai, compare Brandt Chlorophyll bei Thieren. BY R. VON LENDENFELD, PH.D. 323 Amoeboid wandering cells, very much like amoebae with lobate Pseudopodia are common in all parts of the Sponges, their function is merely to serve as vehicles of food and oxydized substances, as we shall see in the chapter on Physiology. Some of these cells are developed into the generative elements. The form ova and Spermasacks around which an endothel-like Follicle is formed by other Mesodermal cells. The sperma forming cells are of a peculiar kind (Polejaeff Sper- matogenese von Sycandra raphanus) with a Protoplasm which refracts the light in a greater degree than any other cells. By continuous partition of this cell, finally a heap of small cells are produced, which produce a tail and turn into Spermatozoa. These always consist of a narrow, sharp, lance-point-shaped head and a long tail. The proximal part of the tail is immovable and thick, it tapers abruptly to the thin moving distal part. The ova are not produced in the same manner as the Sperma- tozoa, it is probable that each amseboid cell only produces one ovum. (von. Lendenfeld. Neue Aplysinidse.) All these amoeboid cells, the wandering cells always, and the sexual cells in their young stages creep about very actively in the ground substance of the Mesoderm. Similar amoeboid cells are known in the Medusae, but of course the sexual products do not take their origin from these in the higher Ccelenterata. III. — Embryology. The development of the Sponges, and particularly the first stages, can easily be studied, because the embryos remain within the mother until they have attained a pretty high degree of development. In the shape of oval ciliated Gastrulse they leave the mother and swim about in the sea water for a short time. They then fix themselves to anything suitable and grow out into the Sponge. This latter part of the Ontogenesis is the most difficult to investigate, it is only of late that F. E, Shulze, Keller, and Marshall have succeeded in attaining an insight into the changes which the ciliated and free swimming embryo under- goes before it produces the Sponge. 324 A MONOGRAPH OF THE AUSTRALIAN SPONGES, The cell division does not take place in the same manner throughout. In the Calcispongire the young Morula consist of a ring of cells with a hole right throiigh the centre, connecting the oral pole of the larva? with the aboral. In other Sponges such a stage does not exist, but only a solid morula which produces secundary in the interior, a space, or a Furchungshohle. All Sponges seem, however, to pass a Blastula stage. The single layer of cells which constitutes the wall of the Blastula may be produced by the coalescing of the oral and aboral apertures (Calcispongiae), or by the ordinary process of an imbibition of water by the solid morula. In the central mass, which Marshall calls Ccenoblostem, first Nuclei seem to make their appearance. Marshall thinks that the whole Ccenoblostem resembles a Syncitium. Other observers are inclined to consider these "Nuclei as belonging to cells, the limits of which escape observation. In this state the embryo leaves the brooding place, swims about for some time in the canals of the mother and finally leaves them. The cells of the outer layer, which now can be called Ectoderm, produce one cilia each, and the movements of these cilia propel the young Sponge. In some groups (Ceraospongiae, Reniera, and other Silicispongiee) the embryo has a pigmented spot on one end of the oval body, which might perhaps be considered as an eye. The embryos of Reniera filigrana, a Sponge which grows on the lower- side of stones, &c, shuns the light and always seeks the darkest corner of the aquarium. In some cases a ring of particularly long cilia surround the pigmented spot. The bulk of the Ccenoblo- stem increases in size continually and soon bursts the formerly continuous Ectoderm and protrudes slightly from the apertures. The Ectoderm is always torn at the end of the rotation-axis of the oval Embi'yo. The pigmented cells are 'hereby pushed aside and form a ring which surrounds the naked Ccenoblastem. The Ectodermal cells retract their cilia and the embryo, after showing irregular movements for some time, finally affixes itself. The Ccenoblastem flows towards the aboral aperture, which is greatly dilitated and soon sticks to the surface, which the embryo has chosen as his abode for life. BY R. VON LENDENFELD, PH.D. 325 Now a small cavity makes it appearance in the centre of the Ccenoblastem, which may have the shape of a ring (Plakina) or a lens. This original Gastral cavity is perfectly homologous to the Gastral cavity of all those Embryos of other Metazoa which produce their Entoderm by delamination and not by direct invagination. From this simple cavity soon sack-shaped excresences grow forth. The ciliated chambers produced at their termini form short excrescences which connect them with the surface. In this manner tubes are formed, the commencement of the intro- ductory canal system. In a similar manner the Oscular tube is formed from the gastral cavity. As to the further development of the Sponge from this indis- puted stage, there are two opposite opinions, and both from such authorities, that it will be best to state both without commentary. Schulze believes that by a complicated process of continual folding the sponge is finally produced in such a manner that the introductory canals are nothing else than parts of the original free surface of the Sponge, at the sides of which two portions of the outer surface which have come in close contact by the formation of a fold, have coalesced. Marshall on the other hand thinks that all these canals are formed from the ciliated chambers by sending tubes centrifugally, which when they reach the surface open there and so form the introductory canal. The outer surface remaining from beginning to end unfolded and unchanged. Further investigations will be necessary to show which Sponges are developed in the former and which in the latter way. I refer the reader to the statements made above under the heading Ectoderm. IV. Physiology. The investigations on this subject are still fewer in number than those on the former subject, and as yet hardly permit of generali- sation. 1. Skeleton. a. Calcispongice. The skeleton of the Calcareous Sponges consists as the name indicates partly of Calcium. 32G A MONOGRAPH OF THE AUSTRALIAN SPONGES, The chemical composition which is met with in the Sponges, is the carbonic acid salt ; Ca C 03> with very little organic substance, which mainly forms the narrow and often invisible axial canals. The calcareous spicules, which sometimes attain a considerable size, are produced as a secretion by cells and grow by apposition. Ca C 03 and Ca S 04 are always in abundant solution in sea water. These substances are taken up by the Sponge-cells in contact with the water (Canal Epithelpe), and transmitted to Meso-dermal cells, which produce the skeleton. b. Silicisjwngice. The skeleton of the silicious Sponges consists, of Si O., chiefly. There is always an axial canal, composed of oi'ganic substance, and it appears that there are also sometimes concentric layers of siliceous acid and oi'ganic substance intermittent. The young spicules contain more organic substance in proportion than the old ones, and appear therefore softer and can easily be dissolved in re-agents. Also, these spicules seem to originate always in cells, some- tin tes (Hyalonema), they attain a length of 10 Cm. and a thickness of 2-1 mm. They grow, as the concentric layers in their substance indicates by apposition. The silica is procured from hydrate of siliceous acid, Si H^ 03 or from soluble siliceous salt, which are met with in small proportions in solution in the sea water. Si Ka 03 for instance. c. Ceraosponyiw. The horny substance which forms the greater part of the substance in the skeleton of these Sponges, and many of the Monactinellse is a substance similar to hornchitin or silk, F. E. Schulze calls it Spongiolin. Several chemical analysis have been made of it. The percentage of nitrogen is very great. The horny fibres of the Sponges are the product of certain gland cells Spongoblasts, described above, which secrete horny substance. The fibres always consist of concentric layers and grow by apposition only and not by apposition and intussusception. (F. E. Schulze : Die Familie der Spongidee. Von Lendenfeld : Das Hornfaseiwachsthum der Aplysinidpo.) BY R. VON LENDENFELD, PH.D. 327 d. The fibrils of Hircinia. In the European Sponges belonging to the Genera Hircinia and Oligoceras, and also in some Sponges not belonging to these Genera, which I have found on our shores, we meet with a dense mass of fibrillae, long threads with a nob at each end, which may be considered as a peculiar kind of skeleton. They never form the only skeleton of the Sponge, but are always associated with a well developed hornfibre skeleton, and sometimes also with siliceous spicules (Von Lendenfeld das System der Monactinellae.) Their accessary appearance makes it not improbable that they are, or belong to a parasitic organism. The researches which were carried on to elucidate this point at the Zoological Laboratory in Graz, under F. E. Schulze, by myself, and others, did not lead to any positive result. The analysis shows that these fibrils also contain a great proportion of nitrogen. 2. The ground substance. The ground substance appears as a secretory product of the numerous star- shaped cells imbedded therein and has a similar chemical constitution as glue. 3. Foreign bodies. Sponges are often rich in foreign bodies, which may be of any nature, provided they have the proper size. Nevertheless certain Sponges generally select certain foreign bodies. The most common are sand and spicules of other Sponges, which, after the death and decay of these, have dropped to the bottom of the sea. Ceraospongise nearly always contain, more or less sand and other particles in their main radial, sometimes also in their tangental fibres. Sometimes also such bodies are met with in the ground substance of body or skin. They fall on the surface of the Sponge, the Ectodermal epithel cells give way to them, they enter the body of the Sponge and are lead to their place of destination. Particularly interesting are pointed bits of quartz (sand) which are selected with great care. They are always of the same shape, 22 328 A MONOGRAPH OF THE AUSTRALIAN SPONGES, and placed in the skin of a Ceraosponge, with the points centri- fugally as weapons of defence. (Von Lendenfeld, Neue Aply- sinidee.) 4. Digestion. This most important subject is unfortunately also one of the most difficult to investigate. Experiments with carmine-feeding nd other observations seem to show that the digestion is intra- cellular. The carmine particles are taken up freely by all Epithelia of the Sponge, but they are soon ejected from all the cells except those which cover the introductory canals. These cells do not eject all the carmine at any rate, but pass some of it on to the wandering cells which carry it about, dissolve some of the substance (the angular particles loose their sharp edges), and finally seem to pass it on to the cells of the ciliated chambers. Whether the Sub-dei-mal cavities and introductory canals really are the digestive cavity as I believe, or not, cannot yet be known, (von Lendenfeld, Neue Aplysinidae), although my experiments have convinced me of the high probability of it. The cells of the ciliated chambers are in my opinion to be excluded from all functions which have to do with the taking up of nourishment. (Polejaeff Challenger-Calcarea.) Excretary functions and breathing. I assume (von Lendenfeld, Neue Aplysinidse), that the cells of the ciliated chambers are the excretary elements, that they act as kidneys, and I am also enclined to believe that through them the exchange of oxygen and carbonic acid is effected. Their shape, and also other observations point that way. The wandering cells transport the chemical substances which are either necessaiy for the organism or superfluous to the places where the former are wanted and the latter ejected. BY R. VON LENDENFELD, PH.D. 329 V. The Systematic Position of the Sponges. The Sponges are, as I have had occasion to mention above, like all Metazoa, colonies of single cells or roughly speaking, Protozoa. They are very low animals, and so the similarity of them with a congregation of Protozoa is greater than that of higher Metazoa. There has existed since.1867, when Leukart placed the Sponges under the Ccelenterata, a dispute, whether the Sponges are Metazoons or Protozoons. The greatest authorities on the subject consider them as Coelanterata (Leukart, Haeckel, Claus, F. E. Schulze, Marshall, Vosmaer, Ray Lankaster), whilst others, particularly the majority of English authors, who in otio cum dignitate, do not take much notice of what anyone else does (O. Schmidt, Vorwort zu den Spongien des Meerbusens von Mexico), and the Americans consider it ridiculous to call the Sponges Ccelenterata, but persistently call them colonies of Protozoa. To me this dispute seems very useless, and in fact ridiculous. Of course the Sponges are colonies of Protozoa, but so are the Medusae and corals ; of course the sexual propagation is initiated by conjugation — but so it is in the Medusae and corals. Of course the Sponges consist of a zoaglealike ground substance in which cells are imbedded and which is surrounded by Epithelia — but so do the Medusae and corals. There are of course great differences between Medusae and Sponges — but are there not as great difference between a parasitic cirrhiped and a lobster 1 Among the essays on this subject which have been published recently, there is particularly one which I shall translate here, because it points out the matter so clearly and simply. (Marshall, Die Ontogenesis von Reniera filigrana. Zeit. schrift fur wissenschaftliche Zoologie Band, XXXVII. Seite, 239-216. It is known (but it does no harm to point to it from time to time) that Leukart (1) drew attention to the fact that the Porifera belonged to the Ccelenterata in the first instance. This was in his review of Lieberkuhn's Essays on the Anatomy of the Calci- spongi . (1.) Jatresberichte, 1SG4-65, p. 196 and 197. 330 A MONOGRAPH OF THE AUSTRALIAN SPONGES, Here he follows the results gained by this author " in die letzten Konsequenzen hinein," and proves his theory for the first time in a decided manner. He, in the first place, drew attention to the homology between the ciliated cavity of the simple Calcispongiae (Grantise), and the gastral cavity of a Hydroid Polyp. He compai-ed the mouths of these two with one another, and he dwelt on the accessory difference between them ; that in the one case tentacles surround the mouth whilst the other has no arms. The pores of the Sponges he compares with the numerous cases of waterholes in the Ccelenterata. (1.) " Allerdings," Leucart continues : — " Sind nun nicht alle Poiiferen so einfach organisirt, wie die Kalksckwamme, vielmehr ist die Mehrzahl derselben mit eniem Hohlensystem versehen, welches mit der weiten Leibeshohle der Grantien und Syconen nur geringe ^Ehnlichkeit hat, allein es ist zur Geniige beckannt, dass der coelenterische Apparat auch soust durch peripherische Ausstiilpungen und Verastelungen die mannigfachsten Formen annimmt." In these words nearly everything is contained that concerns the comparison between the morphological structure of the Sponges and the Coelenterata ; only that these ideas can be further worked out and that a few words can be added about the Ontogenesis and Phylogeny of these two large groups. Balfour (2) is inclined to consider the Sponges as a type of Metazoa developed separately for itself from the Protozoa. And this appears to him to be proved by the following facts : — (1.) By the peculiar structure of the free larvae ; (2.) By the early development of the Mesoblast in the Sponges, and particularly (3) by the remarkable structure of the digestive canals. As far as the first reason is concerned, I am not inclined to consider it as sufficiently general ; the remarkable pecularities of (1.) Haeckel, who, extraordinary to say, did not know Lenkart's deduc- tions, compares six years later the Sponges and Acalephes in nearly the same manner. Kalkschwiimme. Band I. Seite 462, M.A.O. (2.} Balfour. A Manual of comparative Embryology, Vol. II., p. 309. BY R. VON LENDENFELD, PH.D. 331 the larvse of Sponges compared with those of other Coelenterata are only met with apparently in the Calcispongise. The Cerao- spongiae have precisely the same larvse as some higher Coelen- terata, Eucope for instance. Of course one might consider the larva? of Eucope as consisting of two layers, and Balfour does that, but it is the cpiestion whether this procedure is not somewhat arbitrary. One might consider it also in the following light : Into the cavity of a Blastosphsera cells enter from the Ectoderm, which in time fill this cavity, and in this manner form a coeno- blastem. Now delamination occurs in this coenoblastem and hereby it separates into a Mesoderm, and an Entoderm which surrounds the delamination cavity and (conipai'e also Kowalensky's original plate, fig. 8) consists of cells, which 'are differentiated in another manner as the cells forming the Mesoderm. Also the second reason of Balfour's admits of a discussion. The Sponges are a very old branch of the Coelenterata and for a long time sessile in the adult stage, probably for a longer time than any other sessile Coelenterata, as we can easily conclude from the early time of the affixing of the larvae and the numerous adaptations which the Sponges have attained in connection with this way of living. The sessility again caused the appearance of a skeleton here as in nearly all other cases where animals become sessile, which, whether it be of a calcareous, silicious, or horny nature (with the exception of a few very rudimentary Sponges) increased in size and density, from generation to generation, as most important to the Sponges. But the skeleton is not only a product of the Mesoderm of these organisms, it is even its principal product, and so the Mesoderm must have also increased in importance and size, the more the Sponges ceased to be solitary individuals and the more they commenced to form colonies, until it finally, as we see in many adult Sponge-colonies, overgrows the gastral cavities and depresses them nearly to a rudimentary organ. The otherwise rare obliteration of mouth and gastral cavity which is sometimes met with, is caused by changes which have taken place in their function in the Sponges. These changes 332 A MONOGRAPH OF THE AUSTRALIAN SPONGES, have caused the original water holes of the Coelenterata to assume the function of taking up nourishment, whilst the digestive functions have been assumed by the Epithelia of the coelenteric canals. (1.) Another consequence of this change of function is the wonderful variety in shape which we meet with in the Sponges. Intercanal system, Pseudogastral cavities, &c, are transformed in all these changes, the outer surface of the Sponge always inci-eases in size, and the number of pores through which nourishment is taken up is increased. The sum of all these peculiarities not only favoured the development of the Mesoderm but it was an efficient cause. This deduction only would explain why the Mesoderm in the adult Sponges appears so much more developed than the other layers, but it would not be sufficient to disprove the second reason of Balfour's why the Sponges cannot be Coelenterata. For this it is necessary to consider certain laws of heredity. The law of heredity in the corresponding age (Haeckel's homochrone law) may be correct in general, but appeal's to be modified in some cases, particularly if it is in competition with settled hei'edity. This later kind of heredity has the inclination to let peculiarities appear earlier and earlier from generation to gene- ration, if these are particularly advantageous to the organism. The sooner the progenxj attains j)ossession of peculiarities which have shown themselves as useful for the ancestors, the better for them. (If not a pure recapitulation of the Phylogeny offers still better chances.) This is the main cause of the series of appearances called " shortened heredity." These peculiarities do by no means always appear in so striking a form, as for instance, among the crustations, they form moreover a finely shaded series, corresponding to the infinite variable conditions of existence in the living beings. ( 1 . ) The whole process of this retrograde development can be compared to certain consequences of Parasitism . BY R. VON LENDENFELD, PH.D. 333 It follows from this that the high development of the Mesoderm of the Sponges which has doubtlessly been developed and fixed in such a degree, during a very long series of generations, must finally have commenced to make its appearance in the larva, particularly if this was not only not disadvantageous but useful for the larva. This latter is doubtlessly the case with the silicious spicules which make their appearance so very early in the larva, and have saved many of them from being eaten. I don't believe that the free ancestors of the Sponges ever possessed a skeleton, this will, according to all analogy, have been formed as a conse- quence of the sessility. The third reason, lastly, which Balfour brings forward to prove that the Sponges are not Ccelenterata, is therefore of particular interest, because it is one of those which induced Leukart to decide for the Ccelenterate-nature of the Sponges, only that the one author puts the differences between the development of the gastral cavity in Sponges and Ccelenterata forward, whilst the other attaches particular importance to the similarity of the two ; but we know that when we have to do with modifications of homologous organs, as evidently in this case, the affinity must be considered as a proof of the old genetic connection, and is therefore the essential part, whilst the difference points to a special attainment, and is therefore accidental. In both groups we see that a canal system has been differentiated which extends centrifugally from the gastral cavity, which often penetrates the Ectoderm (in Sponges, with the exception of the problematic Physemaria always), and which opens with constant or variable pores outward ; where tentacles are met with, the canal can enter them and here (Actinia) or also in other places (Rhizostomse), can open outward with pores ; and as in the latter case astomy occurs, nourishing materials are taken up through these pores just as in the Sponges. Ciliated cells are widely spread in the gastral cavity of Ccelen- terata, if they also don't mass themselves locally to form ciliated chambers. But this is also by no means the case with all Sponges. 334 A MONOGRAPH OF THE AUSTRALIAN SPONGES, (1.) If Balfour (2) says that the ciliated cells which cover the ciliated chambers or radial tubes of the Sponges undoubtedly originate from the invaginated cells (i.e., the ciliated cells of the Ectoderm), then I would like to state that they certainly did not originate from those, they are moreover in Sponges and Ccelenterata modified elements of the Ectoderm which may be produced originally from the Ectoderm in some cases, (invagination) but not necessarily must be produced by the Ectoderm (delamination.) If we once more compare the canal system of Sponges and higher Ccelenterata, we shall see that it can open outward free in both, that it can be covered with entodermal ciliated cells for a greater or smaller extent, and that lastly it can take up nourish- ment through its tei'minal pores in both. Another reason which is generally brought forward against the Ccelenterate nature of the Sponges is, that the Sponges never possess tentacles or Cnidoblasts. Without placing too great a weight on the want of both in Beroe' which is a rudimentary form in this respect I only wish to discuss : Have the ancestors of the Sponges ever possessed tentacles and Cnidoblasts ? and if yes, how have they lost them ? If no, why were these not attained in the course of time. Cnidoblasts or their Homologa, respectively Analoga and tentacles are so widely spread among low marine animals, and are met with in so very different animals, that they cannot be used as a determinant for the relationship, as they are arrange- ments doubtlessly often attained sua sponte. But as they are met with in higher Ccelenterata (3) in different modifications, nearly without exception, they appear to be a very old peculiarity of these animals, which has proved itself as very useful in the struggle for existence, and which therefore could find such a wide distribution by heredity, in some cases perhaps by an adaptation sua sponte. (1.) Kiilliker. Icones Histological. 1 Heft., p. 66. (2.) F. Balfour, I.e., Vol. I., p. 144. (3. ) Which might be separated from the Sponges as Telifera or as Nemato- phora, Huxl., (because the name Cuidaria, nettle animals does not cover the meaning.) BY R. VON LENDENFELD, PH.D. 335 The great phylogenetic age of these nettling organs is made likely by the fact that the Cnidoblasts are met with already, in the free swimming larvae of some species, which is to be considei'ed more as an exception than as the rule. This appearance of Cnido- blasts in the larvae is probably produced by a very long-continued heredity, as this happened in an analogous manner with the mesoderm in the larvae of the Spongise, as mentioned above. According to my idea, Cnidoblasts and their Homologa have been developed in connection with the tentacles firstly in the adult animal, as they have again disappeared in Beroe', together with the tentacles (1) they are parts of these (according to Chun, modi- fied muscular cells) which have been changed in such a remarkable manner for purposes of catching prey. That they afterwards should have attained the functions of defensive weapons, and should then have been distributed all over the body does not appear so very wonderful. (2) It is certainly difficult to ascertain whether the Sponges are — as not possessing tentacles and Cnidoblasts — rudimentary in this respect or not ; whether their ancestors possessed them or not ; is not of very great importance, this does not seem to have to do with the question whether the Sponges are Ccelenterata or not, In the ontogenesis of the Sponge we never find a stage where anything homologous could be met with, just as little as we find any trace of anything of the kind in the adult Sponge. But both these facts do not prove that they really never had been present : also here the ontogenetic image of the Phylogeny might be dirnned, by a very long continued uselessness. It is, in case that the Sponge-ancestors rarely possessed these organs, not difficult to understand how they have been lost. (1) If Protohydra, accepted as an adult animal, had been as lively and energetic as Beroe, also that animal could dispense with the protection of Cnidoblasts if it had no mouth-arms. But, if in reality the tentacles were the primary, and the Cnidoblasts the secundary thing, then Protohydra is certainly not an ancestral but a rudimentary form. (2) Compare Cnidoblasts and their distribution among Ccelenterata, Pagenstecher Allgemeine Zoologie, Band II., pp. 24-27 ; particularly Band IV., pp. 259-263. Chun, Mikroskopische Waffen d. Coelenteraten, Humboldt, Band I., Heft 2, 1882. /£: i- • •-. * va