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MARINE INVESTIGATIONS IN SOUTH AFRICA. VOL UME ~V. WITH TWENTY PLATES. NoV 26 1910 Ne ANS |S Neree Sia) Muse” Salva 861 | o NWE CAPE TOWN: PUBLISHED BY THE SOCIETY. 1908. CONTENTS. THE OPISTHOBRANCHIATA OF SoutH Arrica. By R. BEercu A New Species or Planocera (P. Gilchrist?) rrom SoutTH Arrica. By Lypia JAcupowa. ; New Forms or THE Hemichordata From SoutH AFRICA. By J. D. EF. Giucurist On A Parasitic Coprrop FRom Cephalodiscus. By W. T. CALMAN On tHE GENUS Botellina (Carpenter), with A DESCRIPTION oF A New Species. By F. Gorpon PEARCEY PAGE 145 151 177 185 5) SBWTORIAL NOTE. y a Volume VI of the Marine Investigations will 7 be published in the Annals of the South African “Museum. ane . oe ys - = al a ies + 7 : PP here igs > “ee NC mee. Y 4 a q d * Fix R 4 ’ Ps THE OPISTHOBRANCHIATA OF SOU TE ARP RIGA. BY R. BERGH, Coprnnacen. (Wire FourtEEN PuatEs.) The number of Opisthobranchiata hitherto known from the coast of South Africa is very small. Krause described a Plewrobranchus granulatus, Vayssiére a Plewrobranchea capensis, Rang a Melibe rosea, Stimpson a Tritonia pallida and a Triopa lucida. The investigations of late years of the Cape Government, carried out under the direction of Dr. Gilchrist, have considerably aug- mented the number, and have furnished the material for the following report. The East and South Coasts of South Africa are washed by a prolongation of the great equatorial current from the Indian Ocean ; the West, on the contrary, by the cold Antarctic current. Some- times, however, it happens that the warm Agulhas current passes up this side, while at other times the cold Antarctic current passes further to the Hast.* In general there is a marked difference * Gilchrist, ‘‘ Observations on the Temperature and Salinity of the Sea around the Cape Peninsula.” Mar. Inv. I., 1902, pp. 181-216. Gilchrist, ‘‘ Currents on the South African Coast, as Indicated by the Course of Drift Bottles,” part ii, 1904, pp. 155-166. iI 2 Marine Investigations in South Africa. Vol. V. between the fauna of the West side of the Cape of Good Hope Peninsula and that of the East. The latter has more of a tropical Indian character, the former a somewhat more Northern, although typically tropical forms of Nudibranchiata (e.g., the Melibe) are not wanting. TECTIBRANCHIATA. ANASPIDEA. APLYSIIDA. APLYSIIDZ PROPRIA, I. Apuysia, L. Linné, Syst. Nat., ed. xi., 1767, p. 1072. Cuvier, Tableau Elém. (1798) an v., p. 386, pl. ix., fig. 3. Lamarck, Syst. des Anim. s.v. 1801, p. 62. R. Bergh, Die Opisthobranchiata der Siboga Expedition, 1905, Duos 1. Apu. GincHrRIsTI, B. n. sp. Animal colore brunneo albo-maculato. Pied igs. 1-37 ele shige A living specimen was procured in False Bay in February, 1905 (Pl. X., fig. 1). It was brown in colour, the sides of the foot with many small white spots and white border, the outer border of the wings with larger white blotches, and many fine black perpendicular lines on their outer side. It swam dexterously and at a fair speed through the water. The animal, in a contracted condition (preserved in formalin), had a length of 6:5 cm. and, with raised parapodia, a height of 3 and a breadth of 2°5; the breadth of the head (with its 7 mm. long tenta- cles) 2 cm., the height of the rhinophores 6 mm., the length of the mantle-shield 2°5 cm., its breadth 2, the length of the sipho 1, the breadth of the foot proper (sole) 9 mm., the length of the tail 8, the length of the foot-wings 4 cm., with an inside height of 1-7.— The colour of the sole of the foot is blackish brown with a whitish margin, the animal otherwise of a dark brown colour, whitish rather elongate spots on the sides of the body, some also on the outside of the wings and a series of larger blots along the margin, the inside of the wings of the same brown colour with afew whitish spots towards Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 3 the whitish margin, the mantle and the sipho of somewhat brighter brownish colour with spread roundish whitish spots. The animal has large, rather flattened tentacles, the sole of the foot not narrow, with distinct margins, the wings high, meeting behind and connecting with the tail; on the mantle no aperture could be detected, the somewhat grayish gill 22 mm. long by a height of 10 and a thickness of 6, nearly its half freely projecting, the number of groups of lamellee about 15. The shell 2°3 cm. in length with a breadth of 2 and a height of about 0:5; of quite usual form, with a thin calcified, very fragile layer and a rather large cuticular margin. The eyes of a diameter of about 1 mm. The length of the mouth tube 3 mm. The bulbus pharyngeus erayish, 9 mm. long, with a height and a breadth of 6. The mandi- bular plates larger, meeting above and beneath, 4:5 mm. high with a breadth of 2:25; their full anterior half black brownish, the rest yellowish ; their staff-formed elements up to at least 0-2 mm. high by a diameter at the slightly thickened upper end of 0-016. The gray palate as usual, its plates with the usual thin hooks of a height of up to at least 0°2 mm. The brownish yellow rasp of the broad tongue containing about 36 series of plates, in the short and thick sheath 10 series, the total number thus being 46; in the series up to 33 plates. The plates in the thicker parts yellow ; the breadth of the median 0-28 mm.; the 4 outermost measured 0:08—0:12-0°18, and 0-25 mm., the length then rising to 0°35 by a height of 0°24 mm. The median plate (Pl. I., fig. 1) not broad, with finely denticulated hook and two denticles at its root. The two outer plates (fig. 2a) without hook, the next with a small single one, the following with denticular hook (fig. 2). The plates otherwise of the usual form, with pointed finely denticulated hook and a stronger denticle towards its root or (on the outside) with 2-4 (fig. 3). The long thin white salivary glands as usual. The black cesophagus 10 mm. long by a breadth of 1:25. The first stomach nearly colourless, 14 mm. long by a diameter of 10, empty. The masticatory stomach, brownish gray, 8 mm. long by a diameter of 6, two series of rather low thorns before the cardia, the facets of the stomach as usual, with 8 larger and about 6 smaller plates, the larger of about the same size, of a height of 3-5 mm., dirty yellow, the smaller paler, less regularly pyramidal. The third stomach 5 mm. long and broad, without facets, as it were. The brownish gray conical (aver 14 mm. long by other diameter of 9, the end of the long (about 4 mm.) gall-bladder freely projecting on the surface of the liver, 4 Marine Investigations in South Africa. Vol. V. The yellow hermaphrodite gland covering the end and the hinder upper side of the liver with a layer 4 mm. thick, 8 mm. long, and 7 mm. broad, its duct long and strong. The yellowish white and grayish anterior genital mass as usual, the grayish globular spermato- theca 6 mm. in diameter. The brownish gray penis 11 mm. long by a diameter of 2°25, nearly cylindrical, the inside of the prasputium with strong blackish longitudinal folds ; the white glans 7 mm. long, very pointed, somewhat turned, with rather deep furrow. 2. APL. ALLOCHROA, B. n. sp. Pl. I., figs. 4-10. Two individuals of nearly the same size were caught at Knysna at low tide on the shore between the jetty and the village. One of them gave off a good deal of red pigment. The length was 25 mm. with a breadth of 10 and a height of 11, the oval mantle 12 mm. long, its round hole of a diameter of 8, the sipho 4mm. long by a breadth of 3, the length of the somewhat flattened gill 5 with a breadth of 2 mm.; the foot 4 mm. broad, the wings 13 mm. long, their height (on the inside) 5, the length of the tail 4. They were one-coloured, yellow, merely the cleft of the rhinophores and the tentacles black and on the free inner margin of the foot-wings a series of small black spots, the gill slightly brownish. The skin quite smooth all over. The foot-wings coalescent behind. The under-side of the mantle brim brown, richly provided with small glands. The shell (fig. 4) very difficult to see and to loosen, 11 mm. long with a diameter of 9, very flattened, very thin cuticular, with small nucleus, without any trace of calcification, nearly colourless. The central nervous system as usual. The bulbus pharyngeus dirty yellowish, 5 mm. long with a breadth of 3°5 and a height of 3; two grayish, as it were, palate plates shone through the roof of the mouth cavity, but no trace of armature could be detected. The longish triangular mandibles brown, anteriorly nearly black, 1°75 mm. high by a breadth up to 1, their elements (fig. 5) up to 0:18 mm. in height by a diameter of 0:009. The rasp of the tongue yellowish brown, containing 22 rows of plates, in addition 15 in the sheath, the total number of the series thus being 37; about 20 plates in the rows. These last with exception of the 2-3 outer brownish yellow; the length of the 6 outer (fig. 8) was 0-06—-0-08-0:1-0°12-0:'18-0°25, and seemed not to become higher, the breadth of the median plates 0:35 mm. These last (fig. 6) with Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 5 finely denticulated hook and at the base of this two pointed denticles. The first lateral plates (fig. 7) with strong hook finely denticulated on the margins and at its base two strong denticles. On most of the lateral plates the margins of the hook were even, but at its base two pointed denticles on each side; the 4-5 outer (fig. 8) had no hook. The salivary glands as usual. The first stomach 8 mm. long by a diameter of 7, at its pylorus two series of irregularly roundish facets. The masticatory stomach brownish, of a diameter of 3 and a length of 2.5 mm., showing 9 larger and 4 smaller plates, all yellow, the first up to 15 mm. high, of the usual pyramidal form, the later partly more conical (fig. 9). The third stomach 2 mm. long, around its cardiac opening a few rounded tubercles; but no thorns could be found. The liver brownish gray, sackformed, 10 mm. long by diameter of 6. The hermaphrodite gland in colour scarcely differmg from the liver, in the male and female lobules ripe genital elements. The somewhat compressed anterior genital mass about 5 mm. long, whitish and yellowish, the sperm-oviduct 6 mm. long. The penis (fig. 10) straightened out 6 mm. long, yellowish, the white glans in its hinder end 1 mm. long, to its posterior end a small prostata gland seemed affixed (fig. 10). This form represents perhaps a new species. 3. APL. GARGANTUA, B. n. sp. RB higs ot Pl, he: at. One individual was taken on the beach at Simon’s Town (2.11.99). Preserved in formalin it had a length of 18 cm. by a breadth of 7°5 and a height of 6:7 cm., the length of the side of the head from the mouth to the end of the tentacles 3 cm. (on each side) by a breadth of 1:8, the tentacles and the rhinophores 7 mm. long. The mantle 7:5 em. long by a breadth of 4:5, its sipho 2°8 em. long with a breadth of 1:8. The gill is of a length of 4 cm. with a height of 2-2, and a breadth of 2, the number of tufts of lamelle on each side about 15. The foot-wings (parapodia) reaching from the region behind the rhinophores to the tail, the height of the wings on the inside up to 3°5 em.—The ground colour of the whole of the back with the wings and mantle clear brownish gray with very many irregular rather large white spots, the upper half of the inside of the wings coloured in the same way here as on the mantle, the spots often confluent in large patches, the lower part of the inside of the wings whitish, the sides of the body grayish, the foot dirty yellowish white. 6 Marine Investigations in South Africa. Vol. V. The form of the animal as usual, the fore end of the head rather large, the tentacles proper and the rhinophores rather small, the male genital opening at the root of the (right) head-wing (about 9 mm. from the mouth). The seminal furrow very distinct, the vulva rather thick. The mantle a little convex, without hole (to the shell); the posterior third of the gill freely projecting, the anal aperture flat, the branchio-pericardial on usual place. The margin on the foot-wings finely crenulated, the foot rounded anteriorly, with pronounced marginal furrow. The shell measured (floating in water) 6 em. in length bya breadth of 4, the height was about 7 mm.; it was quite cuticular, somewhat yellowish, without trace of calcification, the nuclear part very small (fig. 11). The cavity of the body extends to the root of the tail. The central nervous system as usual. The mouth tube 8 mm. long, grayish, darker on the inside. The bulbus pharyngeus 17 mm. long with a breadth of 13 and a height of 12 mm., whitish with gray palate, the thick rasp-sheath forming a prominence on the under side. The mandibles 9 mm. high with a breadth of 4:5 and a thickness of about 0°3, the posterior margin convex, the anterior somewhat concave ; the colour brownish yellow, the anterior half darker; the elements high, rather straight, up to 03mm. long (fig. 12) with diameter of 0:007 mm. The median part of the palate as usual, the thorns of the lateral parts thin, colourless, somewhat bent, of a height up to 0°20 mm. (fig. 13). The large tongue with brownish yellow rasp ; the whole organ was so hardened that a proper examination was impossible; the rasp contained per- haps about 30 and the sheath about 12 rows of plates. The median plates could not be seen; the length of the body of the six outer laterals was 0:04—-0-08—0°10—0:20-0:25 and 0°30 mm., and did not seem to be more ; that of the innermost scarcely exceeded 0°25 mm.; the colour of the plates yellow. The lateral plates (figs. 14-16) nearly of the usual form, with long pointed hook, whose inferior half bore denticles, larger on the outer margin, the upper half with some very fine denticles. The outer plates are much smaller, nearly or quite reduced to the basal plate (fig. 15a). The salivary glands a little depressed, yellowish white, about 4 cm. long, with a breadth in the anterior part of 2 mm., their duct very short. The cesophagus (PI. II., fig. la) rather dark gray, 2 mm. long with a breadth of 5. It dilates suddenly in (fig. 1) the anterior stomach, which is somewhat bent, before smooth, and with some (8) strong circular bands. The length of this rather stiff, somewhat cylindrical Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 7 stomach was 3°5 cm. with a diameter of 1:6 (the gray folds of the cesophagus continued through the foremost part of the stomach. Its cavity was filled with long, whitish, somewhat ramified threads of an alga of a diameter mostly of 0°6-0'75 mm.). The second, masti- catory stomach 1:3 cm. long by a diameter of 2 (fig. 1c); in the cardia a belt of smaller plates, set in 3-5 irregular quincunx-series (figs. 17, 18); behind these the two series of larger plates (fig. 175) ; these last of a dirty brown colour, mostly of the pyramidal form, sometimes (fig. 18) more hornlike, rising to a height of 8 mm.; the plates of the cardial belt smaller, less regular, sometimes pointed- conical rising to a height of 4 mm. The third stomach (fig. 1d) 2 em. long by a diameter of 2°3, its wall thinner than that of the two other; it passes immediately in the intestine (fig. le), which has a diameter of 7:5 mm., and as usual runs in the surface of the liver. The liver blackish gray, black in section, 4°5 em. long by a height of 3 and a breadth of 3°5 cm. The hermaphrodite gland placed obliquely on the hinder end of the liver whitish, of a breadth of 3 cm., with a height of 2, and a thickness up to 12 cm., rather smooth on the free side; in the lobules ripe genital elements. The duct rather short, of a diameter of 4 mm., forming an ampulla with short windings, extending along the whole side of the anterior genital mass. The anterior genital mass large. The muco-albuminous mass oviform, of a length of 20 by a diameter of 11 mm., yellowish in the pos- terior two-thirds, with some (4) grayish spirally circular bands. The strong, nearly cylindrical spermoviduct nearly as long as the whole gland by a diameter of 8 mm., the under half brown, the upper yellowish. The spermatotheca globular, of a diameter of 9 mm., its duct a little longer. The penis a little bent (Pl. L, fig. 19), 15 mm. long, at its hinder end a strong retractor. This hinder end globular, of 3 mm. diameter, whitish; the rest, the preputium, 12 mm. long, grayish. The inside of the praputium darker, with longitudinal folds, of which two stronger are continued in the furrow of the glans; from the bottom of the preputial cavity projected (fig. 20) the pointed head of the glans, show- ing a furrow, which is continued up into the small cavity of the rest of the glans (fig. 21); in retracted state of the penis situated behind the preputium (fig. 19a), it did not show any glandular structure. This form may represent a new species. 8 Marine Investigations in South Africa. Vol. V. 4, APL. LOBATA, B. n. sp. Pl. IL., figs. 8-12. One specimen was procured from Woodstock beach (Table Bay) ; it was preserved in a rather contracted condition. It was 3 cm. long with a breadth of 2°65 and a height of 2; the length of the mantle shield 2:3 with a breadth of 1:7, the length of its hole 6 mm., the sipho about 8 mm. high with a breadth of 10, the height of the foot-wings (on the inside) 14 mm., the breadth of the foot 9mm. The animal was dirty yellowish white in colour. The foot-wings with grossly undulated margin. They both showed at about the middle of their length a perpendicular fissure with a smaller one before and behind. They coalesced posteriorly, and in front nearly covered the head with a prominent lobe 8 mm. long. The mantle very large and prominent; the gill bent, 13 mm. long, with a breadth of 7 and a thickness of 4. The whole body was quite smooth. The shell (fig. 8) of usual form, 2°2 cm. long with a breadth of 1:7, very thin, its calcareous layer broken in many small pieces. The foot-wings were of curious form, lobed and both so sym- metrical that it scarcely could be by mutilation. The gill with about twelve compound pairs of lamelle, the last third freely projecting, the anus and the renal pore very distinct. The bulbus pharyngeus 8 mm. long with a breadth and a height of 6; the mandibular plates 1:5 mm. broad, dirty yellow, their elements (fig. 9) somewhat bent, of a height up to 0°22 mm. with a diameter of 0:013, a little flattened at the point. The palate thorns erect, plump, of a height up to 0:06 mm. The brownish yellow rasp of the tongue contained 32 series of plates, in the sheath 18, the total number of plates being therefore 50, the number of plates in the series 15. The plates yellow, the median 0:35 mm. broad, the length of the basal part of the four outer lateral plates 0-06-0°10-0:14-0:20 mm., and mounting up to 0°30, that of the first (inmost) 0°28 mm. ‘The median plates (fig. 10) with three denticles at the base of the finely denticulated hook ; the lateral plates (fig. 10) with finely denticulated hook, with one denticle at the inside of its root, with 2-3 on its outside ; the 3(—4) outer lateral plates (fig. 11) without hook. The masticatory stomach small, 4 mm. long with a diameter of 4 ; it showed about five clear yellowish white pyramids of a height of about 2°56 mm.; close at the cardiac end 2-3 series of small roundish tubercles. The liver yellow. The penis (fig. 12) 9 mm. long, no armature. This form seems to represent a definite species. Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 9 5, APL. EUSIPHONATA, B. n. sp. BI. figs, 6-15, Of this form one specimen was procured in May, 1902, at Hast London. It hada length of 8°5 em. by a height of 5 and a breadth of 4:6 ; the height of the rhinophores and tentacles was 5 mm., the length of the foot-wings was 6:5, their height (on the inside) 2 cm.; the length of the mantle 3:3 cm., the breadth 2°4 ; the height of the large sipho 2-2 em., its breadth at the base 2°6, at the upper end 1:2 cm. ; the breadth of the foot 2 em.—The ground colour of the upper side, whitish, the head and the neck blackish, due to black partly con- fluent stripes; the outside and inside of the foot-wings with spread rather large irregular black spots; the mantle clear grayish with a few black spots and some black stripes radiating from the centre ; the foot clear dirty yellowish. The form as usual. The foot-wings large, reaching to the root of the very short tail, their margin very slightly undulated, the outside and the inside quite smooth. The mantle of oval circuit, the anterior end a little more pointed, on the centre of the somewhat convex upper side there may be a fine opening; the sipho (figs. 5, 6) very large, embracing a great part of the upper side, fixed to the hinder wall; the anus was seen in the upper part of the siphonal channel; the large mantle quite covered the gill with exception of its pointed end (fig. 6). In the mantle no trace of a shell could be found. The somewhat brownish gill strongly curved, the chorda measured 14 mm., its height 11, its thickness 6 mm., on the underside a broad furrow between the lamelle ; its last fourth freely projecting. The central nervous system as in other true Aplysiz ; the pleural ganglia not half as large as the pedal, lying next to these and before them. The length of the mouth tube 5 mm. The bulbus pharyngeus 10 mm. long by a height and a breadth of 8. The hooks of the gray palate as usual, somewhat grayish, as much as 0°20 mm. high (fig. 8). The mandibular plates strong, brown, broader in the upper end, 4 mm. high by a breadth of 2°5 and a thickness of 0°25 mm. ; their high elements (fig. 7) of a diameter of 0:009 mm. The tongue with brown rasp, containing 28 rows of plates, in the sheath 18, the total number of rows being thus 46; the number of lateral plates on each side of the median about 26. The plates were yellow, only the outer nearly colourless; the breadth of the median 0:25 mm.; the length of the body of the first lateral 0°25, the length 10 Marine Investigations in South Africa. Vol. V. rising to 0°30 mm., the body of the four outer measuring 0:10- 0:14-0-18-0-29 mm. in length. The median plates (fig. 9) some- what plump, their legs rather short, their hook strong, and den- ticulated along the margins; the lateral plates (figs. 10-12) of the usual form, the strong hook with 4-5 denticles at the root of the outer margin, the point with fine denticles, mostly somewhat stronger on one margin; the 4 outer smaller (fig. 13), two without any trace of a hook, and the next with a short one without denticles. The grayish cesophagus 6 mm. long. The yellowish first stomach somewhat curved, 17 mm. long by a diameter of 10. The mastica- tory stomach 6 mm. long by a diameter of 10:5 ; it showed arranged in usual way 10 larger plates and in front 8 smaller; the plates of usual form, pyramidal, of reddish brown colour, of a height up to 4mm. The posterior stomach 8 mm. long by diameter of 7; in its cardiac part fine folds, on the pyloric margin a series of yellow conical and pyramidal plates, 1-1:5 mm. high, always with broken or worn point (fig. 14).—The gray contents of the stomachs formed of different alg, undeterminable detritus and very small sand- particles. The intestine as usual. The dirty dark-gray liver nearly globular, 2-4 cm. long by a breadth of 2-2 and a height of 2 cm. The yellowish white hermaphrodite gland about 14 mm. broad by height of 12 and a thickness of 4; its duct running with its short windings along the whole of the under-side of the anterior genital mass. This last, the albumino-mucous gland, 8 mm. long by a height of 5 and a breadth of 4, yellowish white with the usual spiral white band. The sperm-oviduct a little curved, 8 mm. long by diameter of 2, quite as usual; the short pyriform spermatotheca 3 mm. Jong, the spermatocysta half as large. The yellowish preputium (fig. 15a) 8 mm. long, the retracted glans bent, 4 mm. long, more whitish, with transparent furrow, with strong retractor muscle. The inside of the preputium grayish, in front black, nowhere in the penis any trace of armature. 6. APL. PorKILIA, B. n. sp. Pl. IL., figs. 20-21; Pl. IIL, figs. 1-4. A single specimen was found at Kalk Bay (in Simon’s Bay); it had coloured the preserving fluid brownish. It was 7 cm. long by a breadth of 3 and a height also of 3 cm. ; the length of the tentacles and of the rhinophoria 8 mm. ; the length of the foot-wings 4 cm., by a height on the inside of 1:3; the length of the mantle 3 cm. by a breadth of 2-2; the foot was 1 cm. broad.— The ground colour of the upper side was grayish white, but for the Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 11 most part disappearing through large confluent or anastomosing irregular black spots; the mantle with strong spots and stripes radiating from about the centre; similar markings occurred on the upper part of the inside of the foot-lobes reaching to their margin, the rest being grayish white, as were also the side parts of the body adjoining the mantle; the foot grayish white. The form of the usual type, the foot-lobes free as far as their hinder end; the mantle without hole; the siphonal mantle-fold rather flat, 6 mm. long by a breadth of 2-2; the gill as in the former species. The shell 22 mm. long by a breadth of 20 and a height up to 4 mm. (fig. 1); the cuticular margin rather broad, else the shell was yellow, rather solid, with a prominent nucleal part. The grayish bulbus pharyngeus short, pear-formed, 10 mm. long by a breadth and height of 9. The mahogany brown mandibles strong, 5 mm. high by a breadth of 3; their elements (with a diameter of 0:007 to 0:30 mm.) high, thin, their upper point bent (fig. 20). The palatal hooks nearly colourless, weak and thin, reaching to a height of 0:24 m., by a diameter at the base of 0-035 (fig. 21). The strong tongue contained in the yellow rasp 32 series of plates, in the sheath 22, the total number of the series being thus 54. The 6 foremost series were very incomplete and the plates mostly damaged ; the 6 hindermost in the sheath not quite developed. The number of lateral plates on each side of the median was 25. The plates were yellow, the breadth of the median (between the legs) 0 28 mm., the length of the first lateral 0-26. The median plates (fig. 2) of usual form with serrulated hook, and on either side of it two denticles. The inner lateral plates (fig. 3) were also of the common form, with serrate hook and two denticles at its base (fig. 4). The cesophagus was developed posteriorly into a proventricle. The masticatory stomach nearly cylindrical, 9 mm. long, with the usual armature, the plates faint yellowish. The grayish-brown liver 28 mm. long by a height and breadth of 17. The hermaphrodite gland yellowish white, 15 mm. broad by a length of 10 and a thickness of 4-5 mm. The anterior genital mass yellowish white, 15 mm. long by height of 7 and a thickness of 4 mm.; the yellowish-white spermatotheca globular, of a diameter of 9 mm., the pear-formed spermatocysta 2°56 mm. long. The grayish penis somewhat bent, 15 mm. long; the more whitish glans conical, 4 mm. long (without armature). The colour of the animal, its mandibles, and perhaps the nature of the palatal hooks seem to indicate a definite species. 12 Marine Investagations in South Africa. Vol. V. 7. Apt. Woop, B. n. sp. Pi Th igs: 1319: Together with a specimen of Doridiwm capense, one individual of this Aplysia was procured on the shore, East London (23.5.1902).* The furrow of the rhinophores and tentacles was velvet-black, - otherwise the animal was whitish with scattered traces of gray. Its length was 3 cm. by a breadth of 1:7 and a height of 1:6; the length of oval mantle 12 mm., the length of its oval hole 5, the length of the sipho 5, the gill 14 mm. long by a breadth of 4; the length of the foot-wings 18 mm. by a height (on the inside) of 7. The end of the sole of the foot was developed in a strange way, perhaps pathologically. It formed, as it were, a roundish dise (fig. 13) of a diameter of 9 mm., a little elevated and limited to the rest of the foot on the sides and in front. The wings of the foot passed one into the other behind ; the strong sipho broadly gaping ; the large pallial gland with cells of uncommon size. The rather flattened shell (fig. 14), of a length of 13 by a breadth of 8 mm., very thin, cuticular with very slight and spread traces of calcination, with a small uncalcified nucleus, somewhat pointed in front. The central nervous system quite as in other true Aplysiz. The mouth tube on the outside and the inside dark gray. The bulbus pharyngeus 7 mm. long by a breadth of 4 and a height of 3:0. The mandibles dirty yellow, 3 mm. high by a breadth of 2; their elements (fig. 15) reaching a height of 0°25 by a diameter of 0:013. The rasp of the tongue yellow, perhaps containing 19 and the sheath 18 rows of plates, on each side of the median plates probably about 30 lateral. The plates yellow; the breadth of the median 0:24 mm.; the length of the basal plate of the first lateral 0:20, of the second 0-023; the length of the four outermost 0-05- 0-08-0:08-0-13 mm. The median plates (fig. 16) broad, with short and broad hook, which is serrated as far as the pointed end; the three outermost lateral plates (fig. 19) small, without hook; the other plates are similar in form, have a very pointed hook with a strong denticle on each side; the innermost (fig. 17) had moreover some finer denticles on the outer margin of the hook, which were absent on the rest (figs. 18, 19). The white salivary glands quite as usual. The pharynx gray. The cesophagus whitish, 10 mm. long by a diameter of 4. The first stomach 4 mm. long and broad, at the pylorus * Tt is named after Mr. John Wood, Kast London, who has rendered valuable service in the discovery of this and other marine animals new to science. Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 18 two series of (about 10) short cones. The masticatory stomach 4 mm. long by a diameter of 5; its armature as usual, but the pyramids were nearly all gone; these were of the usual form, clear yellowish, transparent. The third stomach 5 mm. long by a breadth of 3:5; at its cardiac end distinct round impressions left by cones, which were absent. The grayish brown liver irregularly globular, its greatest diameter being 10 mm. ; the gall-bladder whitish. The white hermaphrodite gland 4 mm. broad by a height of 3 and a thickness of 2, somewhat meniscus formed; in its lobules ripe genital elements (zoosperms). The penis whitish, grayish in front. The conical white glans 1°5 mm. long. This form seems allied to the Apl. Siboge (i.c., 1905, p. 9, taf. vi., figs. 36-42; taf. vil., figs. 1-6). 8. APL. MONOCHROA, B. n. sp. Pl. L., figs. 22-24; Pl. II., figs. 2-7. Three specimens were procured at Hermanus on January 15, 1897. Two individuals were dissected. They were of about the same size, and otherwise resembled each other, were uniformly white, except that the inside of the rhinophores and tentacles was blackish brown. The largest one was 4:5 cm. long by a breadth of 2 and a height of 2-5; the foot-wings reaching to the head, 2:5 c.m. long by a height (on the inside) of 1; the length of the oval mantle-hole 7:5 mm. (fig. 22), the white foot 10 mm. broad. The form was as usual; the whole of the back quite even. The shell rather variable in form, thin, in one specimen quite cuticular, in another merely in the two posterior thirds slightly calcified, 18 mm. long by a breadth of 16, rather depressed (fig. 2). Near the hinder end of the mantle-hole, a little to the right, the mantle sends out a sort of siphonal (expiratory) fold separated from the free mantle margin protecting the gill (fig. 22). The curved whitish gil/ 13 mm. long by a height up to 8 and a breadth to 4:5 mm., the rhachis rather strong, on each side about 18 tufts of lamelle ; the gill projecting freely by about a third. The foot rather narrow, somewhat broader in front. The mouth tube 4 mm. long. The whitish bulbus pharyngeus 65-7 mm. long by a breadth and a height of 6; the yellowish mandible-plates not broad, their thin elements of a height up to 0:12 mm. by a diameter of 0-007 (fig. 23). The palate in the middle with the usual network with glands; the palatal plates weak, with 14 Marine Investigations in South Africa. Vol. V. thin, colourless hooks (fig. 24) up to the height of 0:08 mm. by diameter of 0:007—0:016. The rasp of the strong éongue yellow, with 18-19 series of plates, in the sheath 17-18, the total number of series thus being 35-37. In the series 17-18 lateral plates on each side of the median. The plates yellow, the median 0:28 mm. broad; the length of the four outermost (:6—0:14—0:16-0:20. The median plates (fig. 4) of the usual form, with finely denticulated hook and 2-3 denticles at its base. The lateral plates of the usual form (figs. 5-7), the three outermost without any trace of hook, the next with a rudiment, the following of the usual form, but the hook without denticles, which begin on the sixth to eighth (figs. 6-7). The cesophagus in its posterior half developed into a proventriculus. The masticatory stomach nearly cylindrical, stiff, 3 mm. long by diameter of 4; in both individuals eight larger pyramids, bright yellowish up to 2 mm. high, and four smaller, more irregular, mostly bluntly conical. The lover yellowish white, on section yellow, 2 cm. long by a height of 1:5 and a breadth of 1:3-1:5; a small whitish gall- bladder was very distinct. A branchio-renal pore was very distinct deep under the root of the gill. The sub-branchial gland well developed. The hermaphrodite gland white. The proper albumino-mucous mass 9-10 mm. long by a height of 7-9 and a thickness of 4; the sperm-oviduct 10 mm. long; the globular spermatotheca of a diameter of 5mm. The penis long, whitish, at its hinder end a small, apparently glandular, appendix (fig. 3a). (No armature, neither of the small whitish glans nor of the preputium.) The form here examined seems to represent a new species. II. DotaBewua, Lam. Lamavck, Syst. des Anim. s. Vert., 1801, p. 62. Cuvier, Mém. sur la Dolabella &c., Ann. du Mus. v., 1804, p. 435. Rang, Hist. Nat. des Aplysiens, 1828, pp. 45-49, pl. i.-i., xxiv., fig. 1. Bergh, Die Opisthobranchiaten der Siboga Expedition, 1905, « pp. 13-20. Corpus postice latius oblique truncatum ; parapodiis brevioribus, apertura branchiali breviori angustiori. ‘esta pro majore parte nuda, fortior, nonnihil securiformis, margine sinistro crassiori, postice angustior, dextrorsum emarginata et parte nucleali deorsum incurvata carina postica prominenti instructa., Being Transactions of the S. Afr. Phil. Socrety. Vol. XVII. 15 Systema nervosum ut in Aplysiis propriis. Radula (lingue) dentibus medianis elongatis, dentibus lateralibus numerosis non denticulatis.—Glandula hermaphrodisiaca hepati non connata. This animal, with its peculiar form, was first noticed by Rumph (D’Amboin. Rariteitkammer, 2 ed., 1741, N. x., N. 5), who figured the animal as well as its shell, but without any description. On the figure of the shell, given by Rumph, Lamarck established the genus Dolabella, which was adopted by Cuvier and afterwards by malacologists. The form of the animal is quite peculiar, differing from that of all other Aplysiide ; it is posteriorly broader, and terminates in a roundish oblique large disk, to the middle of which the rather narrow, longish branchial slt is continued. The somewhat dolabri- form shell well calcified, with thickened left margin; the hinder part narrower, its right margin is notched; the hind end thicker, bent downwards and to the right, with a sharp, prominent keel. The central nervous system as in the Aplysiz proper. The rasp (of the tongue) has longish median plate and long series of undenticulated lateral plates. The hermaphrodite gland not coalescent with the liver. The genus seems confined to the Red Sea, the Indian and Pacific Oceans. As the form called by Cuvier Dolabella Rumphit cannot now be determined, this name must be reserved for the form figured by Rang. This author has, moreover, drawn up a small series of species (D. Hasseltii, Terenudi, ecaudata* (truncata), and still others have been named by Ehrenberg, Qouy and Gaimard, Sowerby, Stearns (D. Hemprichu, tongana, elongata, californica +); some of them are merely established on the shell, which is rather variable in form, and some are very likely merely varieties of a very widely distributed species. Dou. Rumputt, (Cuv.) Rang, var. (D. Rumphu, Cuv., l.c., p. 487, pl. xxix., fig. 1.) D. Rumphi, Rang, l.c., p. 46, pl. 1. Aplysia tongana, Q. et G., Voy. de l’Astrolabe, i1., 1832, p. 305, pl. 23, figs. 6-7. o * V.d. Decken, ‘‘ Reisen in Ostafrica,’’ iii., 1869; v. Martens, ‘‘ Mollusken,’’ p- 65: Dolabella ecauda, Rang (Zanzibar). + Tryon and Pilsbry, ‘‘ Man. of Conchology,”’ xvi., 1895-96, pp. 151-160, 16 Marine Investigations in South Africa. Vol. V. Dolabella Hasseltii, Fér. Eliot, Notes on Tectibr. and Naked Moll. from Samoa. Proc. Ac. Philadelphia, 1899, p. 515, pl. xix., fee co (Dolabella callosa, Lam. Syst. des Anim., s. v. 1801, p. 62.) Dolabella Rumphu, Cuv., Rang. Bgh., l.c., 1905, pp. 13-20; taf. vil., figs. 22-40; taf. vii., figs. 1-7 (9). Pl. XIV., figs. 10-20. One specimen was procured at Hast London and preserved in formalin. The length of the individual was 12 cm. by a breadth of 9 and a height up to 6:3; the length of the posterior disk was 7°5 cm. by a breadth of 8°5 (the breadth of its brim 1:2); the length of the branchial slit 7 em. by a breadth at both ends of 1; the height of the sipho 9 mm., that of the parapodia 13, of the (contracted) rhinophoria 6 mm. ; the length of the curved gill in a straight line 3°5 cm. by a breadth of 2°3 and a thickness of 1°83 cm. The animal was one-coloured, yellowish white, the gill less bright. The shell of typical form (figs. 12, 13), 4°3 em. long by a breadth of 3:3; the crest on the hinder end not strong ; the calcareous layer on the under side of the strong yellowish cuticula broken in pieces in front, the upper as well as the under side of the shell chalk-white. The form of the animal was typical, the branchial fissure reaching to about the middle of the hinder disk. The back with rather numerous (fig. 11) small pointed cones of a height of 2-4 mm., as also the hinder disk, as well as its somewhat laciniated brim (fig. 10). The seminal furrow in its first part running in the depth between the parapodia for a length of 2 cm., then continued forwards to the male genital opening under the right tentacle. The mouth, the sipho, the anus, and the pallial gland as usual. Nearly the posterior half of the gill projects freely ; on either side it showed about ten strong compound chief lamellae; at the base of the frenulum of the gill the reno-branchial aperture. The common genital opening as usual. The central nervous system agrees with that of the true Aplysiz, and is quite different from that of the Notarchide, with which group the Dolabelle otherwise show affinities; the visceral ganglia thus situated far backwards (on the side of the spermatotheca). The nearly coalescent cerebral ganglia measure in breadth nearly 4 mm. ; the cerebro-pleuro-pedal connectives about 13 mm. long ; the pleuro- pedal ganglionic mass 8 mm. broad ; the pleural ganglia scarcely half as large as the pedal.* * Cf. Amaudrut, Bull. Soc. Philom., x., 1886, pp. 68-74, Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 17 The very retracted and contracted mouth tube about 7 mm. long. The plump bulbus pharyngeus 15 mm. long and high by a breadth of 12, of usual form, with the end of the rasp-sheath somewhat prominent on the lower side posteriorly ; the strong inferior retractor muscles of the bulbus issuing from the region of the margin of the hinder disk of the body. The strong, somewhat brittle mandible plates of a length of 7 mm. by a breadth of 3°8 and a thickness of 0-4 mm.; they were yellowish brown on the free side, on the breach yellowish white; their closely set angularly cylindrical elements of a diameter of 0:016 mm. (fig. 19). On each side of the palate a thin, dirty yellowish plate, 3 mm. broad, densely set with (fig. 18) horny, compressed hooks, of form as in other Aplysiide, of a length up to 0-8 mm. by a breadth to 0:10. This spinous covering continued a little behind the roof of the pharynx. The large tongue with deep cleft; the rasp brownish yellow, containing 42 se ies of plates (counted at the margin of the rasp), in the sheath 44, of which the 5 hindermost are not fully developed; the total number of series about 86; the 6 foremost on the tongue very incomplete and partly damaged. The number of plates in the series seemed to be about 200. The plates were yellow; the length of the median was about 0:20 by a breadth up to 0:07 mm.; the height of the two outermost lateral plates was about 0:14-0:16 mm.; through the series the height of these plates rose to 037 mm. ‘The median plates in form very different from those of the proper Aplysie, longish, narrower in front, with a small denticulated hook at the anterior end (figs. 14, 15); the lateral plates of ordinary hook form (figs. 16-17). The yellowish white salivary glands long, reaching to the cardia, nearly cylindrical, of a diameter of 2 mm., thinner behind ; the efferent duct quite short. The length of the gray @sophagus with its dilatation (proven- triculus) 4 cm. by a diameter of 7-12 mm., its interior with fine longitudinal folds and plump villi. The (masticatory) stomach brownish gray, somewhat roundish, of a (transverse) diameter of 2°5 em. by a length and height of 1-7; the usual nerves run along this stomach, anastomosing at the pylorus and forming a cirele around this, and then continued on the second stomach. The anterior part of this stomach had 8 somewhat depressed angular-roundish facets belonging to the stomach plates, and behind them 2-3 series of smaller and less regularly set facets. The 8 large very hard stomach plates were irregularly pyramidal; the broad basis convex, very smooth; the height and the breadth nearly the same, 7-9 mm. ; the base and the top brown; otherwise the base was chalk-white, 2 18 Marine Investigations in South Africa. Vol. V. Behind these plates 10 somewhat smaller followed, mostly rather compressed, more irregular, yellow, of a height of 4-6 mm. Behind this stomach, in the mouth of the second, more thin-walled gray stomach, were seen about 5 series of rounded small papillae, each with a pointed, straight, yellow prickle of the height of 2-256 mm. (fig. 20); papille of the same kind, mostly without horn, were scantily distributed over the stomach. The abundant content of the stomachs was fine paunce mixed up with vegetable substance (different algae), parts of small worms, and some foraminifera and small Rissoa-like shells. The dirty gray intestine makes a large superficial curve in a furrow of the liver and ascends to the anus ; its diameter 7-9 mm., its wall thin, its abundant contents the same as in the stomachs. The large liver dirty and dark greenish gray, 5 cm. long by a breadth of 4 and a height of 3°8, superficially 3-lobed by the windings of the intestine ; its mass compact, with a small cavity. In front, immediately behind the second stomach, opens the bent, horn-shaped gall-bladder, contrasting by its milk-white colour with the liver, of a diameter of 4 mm., with about its half freely projecting on the under side of the liver. The bright yellowish white kidney 3°3 cm. long by a breadth of 2°3 cm. and a thickness of 5-6 mm. The yellow-white hermaphrodite gland at the hinder end of the liver convex-plain, 4°5 cm. long by a breadth of 2°5, and a thickness of 2; in its lobules ripe genital elements. The thick hermaphrodite duct in corkscrew windings running to the anterior genital mass; its diameter mostly 3°5 mm., anteriorly much thinner. The anterior genital mass large, 3°5 cm. long by a height of 3 and a thickness of 1:5; chiefly formed by the large muco-albuminous gland. On the right side of this appeared a black central region of oval form, 11 mm. long, encircled by alternately more whitish and more yellowish arcuate windings; the left side more simple with a large winding. The curved sperm-oviduct extended 5 cm. long by diameter of 8-4 mm.; on the cuts two tubes, separated by an incomplete septum, appear. The spermatotheca, situated immedi- ately before the pericardium, globular, of a diameter of 15 mm. The dark grayish pems (preputium) folded up extended 5 cm. long by diameter of 7-4 mm.; to its posterior end, which is yellowish, the strong retractor is attached, to its anterior end the digitations of the protractor. The inside with fine longitudinal folds and a thicker one, all with a number of black points. From the bottom of the cavity projects the flattened, blackish only at the point, else yellowish, somewhat strained glans, extended 15 mm. long by a Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 19 breadth of 5; one margin is thick, compact, otherwise it is flat, leaflike. The colour of this specimen was different from those I also have seen *:; the form of the shell, too, somewhat particular, and the stomach-plates different. Still, it is very likely but a variety of the somewhat variable Dol. Rumphiw (Cuv., Rang). NOTARCHIDAi. R. Bergh, Die Opisthobranchiata der Siboga Expedition, 1905, pp. 20-27. This group contains the genera Notarchus (Cuv.), Aclesia (Rang), Aplysiella (P. Fischer), and Phyllaplysia (P. Fischer). AcussiA, Rang. Rang, Hist. Nat. des Aplysiens, 1828, p. 68, pl. xx.—xxii. R. Bergh, Malacolog. Untersuch. V. 1900, pp. 302—-00!.—The Danish Expedition to Siam, 1902, pp. 168-174.—Die Opistho- branchiata der Siboga Expedition, 1905, pp. 20-23, Notzum sicut rhinophoria et tentacula papillis majoribus simpli- cibus et compositis instructum ; fissura branchialis brevis. Scutum palliale sicut testa desunt; branchia, ren et pericardium in cavitate branchiali libera (scuto non tecta). Podarium non angustum. Ganglia visceralia antice, inter pleuralia sita. Penis conulis hamigeris armatus. The genus was established by Rang, and the plates xx.—xxii. have the name of Aclesia; in the text he has (p. 68) retracted the name, referring the species named in the plates to the genus Notarchus of Cuvier, to which, however, they do not belong. The genus has mostly been adopted by malacologists and con- chologists + for forms like those originally given by Rang, but a real knowledge of the genus dates from the later years (1900, 1902, 1905). The HH ww bo 5 . End of glans. (132) Puate VIII. DORIOPSIS CALLOSA, B. . End of the everted glans. . Armature in the vas deferens. . Spicula of the skin. (Figs. 1-3 by Cam. 350 x.) Hinder end of the bulbus pharyngeus. 6b, salivary glands, between them the buccal ganglia; c, cesophagus. Doriopsis, sp. . Penis with everted vas deferens. 15/1. . Armature of the glans. DORIOPSILLA CAPENSIS, B. (Figs. 6-7 drawn by Cam. 350 x.) TRITONIDOXA CAPENSIS, B . Fore-end of the animal, from beneath. . Mandible, from the inside. 6/1. . Masticatory edge, from the inside. . Median and first lateral plate. . Lateral plates, from the inside and from the outside. (Figs. 10-12 drawn by Cam. 350 x.) . End of the penis. 100 x. PLEUROPHYLLIDIA GILCHRISTI, B. . Piece of masticatory edge. . Median plates. . First and second lateral plates. . Outer end of two series of plates. . Plate of the inner third of the radula. PLEUROPH. MICRODONTA, B. . Median plates. . Denticles of the same. . First lateral plate of two series. . Hook of lateral plate from the middle of a series. (Figs. 14-22 by Cam. 350 x.) PLEUROPH. CAPENSIS, B. . Median plate. 200 x. . Lateral plate. 350 x. PLEUROPH. EUCHROA, B. . Median plate. 350 x. Opisthobranchiata. PI.VIIL (- Vt — R Bergh. (134 ) Prater. IX. MELIBE ROSEA, Rang. FIG. ; P 2 4 : 1. From the upper side of the cowl with the outer series of cirrhi. a, nodules. 2. Epinotidium. 3. Bulbus pharyngeus with—a, mouth-tube; 6, region of the mandibles ; c, cesophagus. 4. From the inside of mouth-tube. 350 x. 5. The mandibles, from the fore-side, the left overlapping the right. 35 x. 6. a, Gisophagus; 6, stomach with the -plates shining through; c, left biliary duct; d, pocket-like widenings near the pyloric part of e, the intestine. 7. a, Gisophagus ; 6, stomach; cc, biliary ducts. 8, Surface of one of the nodules of an epinotidium. 9. Ramificated renal tube. 10. End of a renal tube. 11. Cells of a renal tube. (Figs. 10-11 by Cam. 350 x.) 12. Last half of the glans penis. 55 x. MARSENIA CAPENSIS, B: 13. From the anterior margin of the mandible. 55 x. 14. Median plate. 15 Median plate from a larger individual. (Figs. 14-15 by Cam. 200 x.) 16, The penis. MARSENIA LEPTOCONCHA, B. 17. Mandible. 9/1. 18. Median plate. 200 x. 19. End of the rasp-sheath. 20, The penis. hth oM., rankfort? Winter, F rer & » = — = « ' * . ‘ ii) 4 A n as = ‘ t . . ‘ a7 - ji : 7 a j ; 1 ‘ - t : ar.» a f 7 é , —— 7 - A im me ~ len s = - rT 4 . - ae ie . - - - a) - - - ~ » 7 i ~<@ +s = ~ - * a * a 7 7 ; + - =a ah = i 7 = = ii = . ie . i - wt . > 7 i =} < 7 ~ 7 2 1 my x. - — < = -y W . 4 : -” = . - — re _ = a ri . _ Ren - = 0 - er : : Sa e < : ; F s a - — i oa st \ a _ 7 7 7 T 7 j . of 7 - : é - S - = = : - aa) ; , - i ot 7 = n- a 7 * 7 ry 7 - 5 - - _ 4) i coal = = - 5 : _ i) =p 7 7 a = 7 — Se. 7 % = ee | a . P oa 1 . = — 7 é oT ° ‘ ? = & : 7 ¥ = vs ~_ - n ‘ - 7 © a 7 s 7 Fa ‘ a - - wm j ' i = = s cc Q — a“, a al ' > I | Q (136 ) PLATE X. MARSENIA LEPTOCONCHA, B. . The shell, from beneath. 1/1. . End of the hook of a lateral plate. 200 x. APLYSIA GILCHRISTI, B. . The animal, when living, natural size and colours, SIGARETUS PLANULATUS, Recluz. . The head with tentacles. . A gill leaf. . From the structure of the gill leaf. 100 x. The penis. . A piece of the mandible. 350 x. . Apiece of the rasp. a, median plate; 6b, lateral plate; c, outer plates. 200 x. . Median plates, from the upper side. . The same, from the under side. . The same, obliquely from above. . The lateral plates. . Outer plates, from the backside. a, interior; b, exterior. . Outer plates, from the side. (Figs. 10-15 by Cam. 350 x.) . The rasp-sheath. i | & | | | : « ; § B. \ iv) < > J2-N ej N 0 pl ASISAILINS [KP N ay ayy! im” i “aa a if’ my ey the (aay: Ty vUP aly ‘ain i} rien bin oir ite at 1M DPA Ge Of ie f . it hy, i Jn Pea i) ar ayy 1 ’ 70, y - A) yi m4 hay, vii an yy 4 Q (138 ) Puate XI, PLEUROBRANCH®A CAPENSIS, Vayss. . Piece of the mandibular plates, from the side. . A piece of the mandibular plate, from the upper end. . One of the largest plates of the rasp, from the margin. . A similar one from the fore-side. . A plate from the middle of a series. . Outermost end of a series. (Figs. 1-6 drawn by Cam. luc. 350 x.) . The preebranchial sac. . End of the internal sheath of the vas deferens. OSCANIELLA NIGROPUNCTATA, B. . Squares of the back, partly withiblack centre. . The shell from the upper side. 9/1. . Serpent-like filaments of the skin of the back. . Element of the mandibular plate, from the upper side. . Similar, from the side. . Similar, from the under side. . Inmost plate of the rasp. . Plates of the inner part of the rasp. . Largest plate from the middle of the rasp. . Outer end of a series of plates. a, outermost of 7 plates. (Figs. 11-18 drawn by Cam. 350 x.) ARCHIDORIS SCRIPTA, B. . The animal, from the back side. 2/1. 20. Spikel of the skin of the back. 1. Plates of the outer part of the rasp. a, outermost. . Plate from the median part of a series. . Largest plate. . Outer end of a series of plates. a, outermost plate. (Figs. 20-24 drawn by Cam. 350 x.) 25. a, Spermduct; 6, penis; c, preputium with glans. STAURODORIS VERRUCOSA (Cuv.). . Plates of the middle of the rasp. . Outer end of a series of plates. a, outermost plate. APHELODORIS BRUNNEA, B. . Innermost plate of a series of the rasp. . Outer end of a series of plates. a, outermost. (Figs. 26-29 drawn by Cam. 350 x.) Qpisthobranchiata. PI. XI. Peis Inv. S.A. ae La fat (140) PratEe XII. APHELODORIS BRUNNEA, B, FIG. 1. Anterior genital mass. a, hermaphrodite duct; 6, muco-albuminous mass; cc, prostata, vas deferens; d, vestibulum genitale ; e, sper- matotheca and spermatocysta. GEITODORIS CAPENSIS, B. . Piece of the lip-plate. . From the inner part of the rasp. a, innermost plate. 200 x. . Plate herefrom. 5. Outer end of series of plates. a, outermost plate. (Figs. 4-5 drawn by Cam. 350 x.) H CO bO TRIOPA LUCIDA, Stimpson. 6. Club-shaped appendix of the back. 7. a, First; b, second lateral plate; c, outer plate. NEMBROTHA CAPENSIS, B. 8. Bulbus pharyngeus, from the upper side. 4/1. 9. Median plates. 10, 11, and 12. Lateral plates in different positions. 13. The outer plates. a, outermost. 14. Innermost (first) of the outer plates. (Figs. 9-14 drawn by Cam. 100 x. 15. Hooks of the penis. 16. a, Spermatotheca; b, spermatocysta. 17. Vestibular gland. EUPLOCAMUS CROCEUS, Phil., var. CAPENSIS. 18. Head with tentacles and fore end of the foot. 19. Arbuscule of the back. 20. Genital papilla with vulva and end of the penis with prominent armature. 21. Mandibular plate. 12/1. 22. Inner part of the rasp with the three lateral plates; and a, the inner- most plates of the outer series. 23. End of the glans. (Figs. 22-23 drawn by Cam. 200 x. 24, Hooks of the glans, 350 x. Aa - ot ie = - MarInv.SA. Qpisthobranchiata. PLXIL R.Bergh Wemer & Winter Frankfort 2M, lit z FIG alg oe w bo 16. (142) Prate XIII. KALINGA ORNATA, A. et H. ‘Papilla of the back. . Tongue with rasp. . Plates from above. . A plate from the side. . Hooks of the glans penis. (Figs. 3-5 drawn by Cam. 350 x.) IDALIELLA AMGNULA, B. . The animal, from above. . The crop of the bulbus pharyngeus, from above. . Elements of the mandibular plates. . From the rhachis of the rasp (lateral plates). . a, Lateral plates ; 6, outer plates. (Figs. 9-10 drawn by Cam. 350 x.) . Glans penis with projecting armature. 200 x. TRITONIA PALLIDA, Stimpson. TRITONIA INDECORA, B. One of the inner plates. (Figs. 13-16 drawn by Cam. 200 x.) ad, glandule salivales. . Left mandible, from the back side a, masticatory process. 3/1. . Piece of the masticatory edge. . One of the largest plates. . One of the outer plates. pa - ~ Mar Inv. SA R. Bergh. Mt 1) i wy Opisthobranchiata. Pl.XII. a ee eee (144) Prats XIV. TRITONIA PALLIDA, Stimpson. FIG. 1. Median and five innermost plates. TRITONIA INDECORA, B. 2. Median and first lateral plate. 3. Two plates of the outer part of a series. DoRIOPSIS CAPENSIS, B. 4. Hooks of the armature of the penis. (Figs. 1-4 drawn by Cam. luc.) MARSENIA PERSPICUA (L.). . Mandibular plate. 55 x. . Hinge part of the same. 200 x. . Piece of the rasp. . Point of a lateral plate. (Figs. 7-8 drawn by Cam. 350 x.) 9. Penis. DTI DonLABELLA Rumpuit, (Cuv.) Rang. 10. Part of the margin of the hinder disc. 11. A papilla of the back. 12. The shell, from the upper side. 1/1. 13. The nucleus, from the under side. 14. Median plate. 200 x. 15. Median plate. 350 x. 16. Lateral plates, from the middle of a series. 17. The two outermost plates. 18. Thorns from the palate. (Figs. 16-18 drawn by Cam. 200 x.) 19. Elements of the mandibular plates. 350 x. 20. Prickles of the cardia of the second stomach. ( 145 ) A NEW SPECIES OF PLANOCERA (P. GILCHEISTI) FROM SOUTH AFRICA. (Pl, XV. figs: 1-7): By Lypia Jacusowa, Archangel. Among the material at my disposal occurred the above Polyclad which had been found by Dr. Gilchrist near the Marine Laboratory at Cape Town. A single specimen only was available. Although considerably contracted, it was on the whole very well preserved both with regard to external features and histological structure. The length of the animal is 40 mm., the breadth 28 mm., and the thickness varies from 1 mm. at the sides to 14-2 mm. in the central region. The form of the body is broadly oval, both ends being similarly rounded ; the margin of the body is strongly folded. It is of a fairly firm consistency and very little transparent. The ground colour of the back of the specimen (preserved in alcohol) is yellowish white. On this are to be seen black spots of irregular shape, and these are grouped together in small heaps equally distributed over the surface of the back. They form a con- tinuous black line only in the dorsal middle line, in the region of the reproductive organs. On the other hand, the region of the brain area is almost devoid of spots and forms a clear unpigmented area. The small spots are also found on the tentacles in very diminished numbers. They are formed of the pigment which lies in the dorsal epithelium of the body in the form of black particles. On the dorsal side of the animal two high pointed neck-tentacles can be distinguished, situated 9 mm. from the anterior end, that is, at the end of the first fourth of the body. The distance between them is 2mm. It is seen by microscopical examination that each tentacle has, at its base, from about fifteen to twenty large, well-developed eyes (fig. 2). The eyes of the brain area, which are not much smaller, are arranged in two rather elongate groups, which lie on the lateral margin of the brain, over which they extend in front and 10 146 Marine Investigations in South Africa. Vol. V. behind. Each group consists of about twenty to twenty-five eye spots. The brain is well developed and surrounded by a strong capsule somewhat flattened dorso-ventrally. It is far removed from the anterior end and is situated near the pharyngeal sac. The anterior nerve cords and the nerves of the tentacles are remarkably well developed. On the under side, which is of a dirty white colour, may be seen, even with the naked eye, the mouth and the genital openings, the female opening being surrounded by a fairly well-developed raised wall. The pharyngeal apparatus is broad and short; it is less than a third of the length of the body and ends close to the male genital apparatus. The pharyngeal sac, which is provided with deep lateral sacs, conceals a strongly folded pharynx, the folds of which are not of any great thickness. The outer mouth lies somewhat in front of the middle of the body and at the commencement of the posterior half of the pharyngeal sac. The gut-mouth is placed somewhat in front of the outer. It leads into a spacious main gut which does not project beyond the pharyngeal sac either in front or behind. It gives off on each side six intestinal branches. The anterior middle branch is rather narrow at that part which les over the brain, and beyond this it gradually becomes wider. The tree-like branched intestinal canals are exceptionally wide, and are, like the main intestine and pharyngeal cavity, quite filled with food material, the origin of which cannot be determined. The reproductive organs occupy a relatively large space. They are altogether about 74-8 mm. in length, or one-fifth of the total length of the body. The female sexual aperture is situated 8 mm. from the hinder end of the body, that is, between its fourth and its last fifth. The male sexual aperture is situated 5 mm. in front of the female, that is, at the commencement of the last third of the body. The penis and the granule-gland (figs. 3 and 7) of the male and the bursa copulatrix (fig. 7) of the female sexual apparatus appear very peculiarly formed. The penis is a large barrel-shaped muscular organ directed backwards. It passes obliquely from in front and ventrally, to the posterior and upwards. On its dorsal wall is a fairly deep fold. The ductus ejaculatorius, which pene- trates the organ, occupies a corresponding position — passing obliquely from in front and ventrally to the posterior and upwards, so that its free end is directed against the dorsal body wall. This position appears to me to be an artificial product, probably brought about by the strongly contracted condition and the consequent folding mentioned above, for the expansion of these parts would Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 147 bring about a more normal and horizontal position in the body. The penis consists of a delicate outer muscular tissue and an inner alongside of the ductus ejaculatorius. The musculature is specially well developed at the base of the penis where the inner joins the outer. The arrangement of the muscle fibres is so complicated that I was unable to determine it with certainty. Radially arranged muscular fibres pass from the inner to the outer musculature, the remaining space between which is filled with connective tissue and parenchyma cells. The free surface of the penis bears chitinous spines and is surrounded by the very spacious antrum masculinum produced by a folding in of the ventral wall of the body. The spines (fig. 5) are small, closely set, and with their points slightly bent forwards. In the neighbourhood of the free end of the ductus ejaculatorius the spines are modified in such a way that they appear in the form of small irregular processes which are twice as long as the spine (fig. 4). The ductus ejaculatorius, which is lined with a cubical ciliated epithelium, extends to the fixed end of the copulatory organ and here divides into a dorsal branch leading to the granule-gland and a ventral branch leading to the seminal vesicle. The granule-gland is rather peculiarly shaped, as shown in fig. 3. It has a central canal with smaller branching canals, which run approximately in the radii of the granule-gland and open at various places in the central canal ; this last leads into the ductus ejaculatorius, into which its distal end opens. The radial canals are surrounded by numerous small glandular cells, the small elongate nuclei of which are situated at their bases. The number of glandular canals is considerable ; ten to eleven are to be seen in median longitudinal section, and they may altogether be present in considerably larger numbers. The thin musculature of the granule-gland consists of longitudinal muscle fibres provided with nuclei. The numerous nuclei of the parenchyma lie on the outside of these. Extracapsular glands are not present. Below and somewhat in front of the granule-gland lies a small oval seminal vesicle provided with a low flat epithelium. Its musculature is constituted of felt-like somewhat loose fibres. Both the vasa differentia open separately into its blind end. Behind the pharynx they turn round and pass into the large seminal ducts. They are short, somewhat coiled canals with a collection of parenchyma nuclei round their epithelium. Anteriorly they extend to the posterior end of the pharynx and posteriorly to the neighbourhood of the female genital opening without however joining here. We have to do with an animal not quite sexually mature, and whose sexual apparatus is not yet quite functionally perfect. The 148 Marine Investigations in South Africa. Vol. V. testes are not well developed, the seminal ducts not broad and con- taining no spermatozoa. The immaturity of the female sexual apparatus is recognised by the limited number and size of the ovaries, as also by the poorly developed uteri and shell gland. The bursa copulatrix of the female copulatory apparatus is in the form of a large strong muscular egg-shaped organ, the pointed end of which is directed backwards. The inner surface of the bursa copu- latrix is provided with rather large closely set papille. The largest lie in the centre of the organ, and they gradually diminish in size towards the anterior and posterior regions. They are provided with a broad basis and are partly drawn out into points and partly more or less rounded off. The papilla are covered with an epithelium which is a continuation of the ventral epithelium of the body, and this varies in different parts of the bursa copulatrix; at its distal end it is extremely flat and its cells are only to be distinguished by their nuclei. Nearer, on the larger papille, it loses its nuclei, becomes thickened and assumes the appearance of a strongly refractive chiti- noid membrane, coloured an intense yellow with picric acid. In its further course it again assumes the characteristics of a flat epithelium, which becomes glandular in character at its anterior end. The papillz in the bursa copulatrix probably serve in some sort of way ag accessory organs of copulation. The anterior end of the bursa copulatrix, which is provided with glandular epithelium, may be regarded as the beginning of the duct of the shell gland, which runs further forward. The shell glands occur in fewer numbers in the epithelium of the duct; in its neighbourhood, 7.e., in the parenchyma, there are however none present. The duct is continued forward to the region of the male genital apparatus, here bending round in a backward direction and passing into the oviduct. This is clothed with a cubical epithelium; at its commencement it includes a common part of both uteri and is continued to a point over the middle of the bursa copulatrix. The accessory vesicle is absent. The uteri consist of narrow canals which do not contain any eggs I was unable to follow them throughout their whole course. This animal belongs to the family of the Planoceride, in which it agrees most closely with the genus Planocera, group A, but it differs considerably from other species of Planocera. The male copu- latory apparatus is characterised by the abnormal structure of the penis and the granule-gland. The difference of the female apparatus from that in other species of this group consists in the peculiar structure of the bursa copulatrix, which is provided with papille, and in the absence of the accessory vesicle. I have named this animal Planocera Gilchristi in honour of its discoverer. ( 149 ) EXPLANATION OF FIGURES. (For all figures.) aeb = anterior enteric branch. b = brain. be = bursa copulatrix. be = brain eyes. cc = central canal of the granule-gland. cht p = chitinous processes of the male copulatory organ. con = connective tissue. dsh = duct of shell gland. eb = enteric branch. em = enteric mouth. fl = flattened epithelium. ¢ = granule-gland. glcl = canals of the granule-gland. glc = glandular cells of the granule-gland. mi = main intestine. mo = outer mouth. msc = musculature. ov = oviduct. oy d = opening of the vasa deferentia into the seminal vesicle. p be = papille of bursa copulatrix. phs = pharyngeal sac. pn = parenchyma nuclei. ps = penis. sd = seminal duct. sp = spines of penis. sv = seminal vesicle. t = testes. te = tentacular eyes. ut = opening of uterus to oviduct. yd = vasa deferentia. = male genital opening. ? = female genital opening. Prats XV. FIG 1. Longitudinal section. Enlarged ca. 5. . Sketch of anatomy. . Granule-gland, median longitudinal section. Obj. 3, Oc. 3. . Chitinous processes round the ductus ejaculatorius. Obj. 5, Oc. 0. . Spine of penis from a longitudinal section through the copulatory organ. Obj. 7, Oc. 3. 6. Longitudinal section through the bursa copulatrix. Obj. 2, Oc. 0. 7. Schematic representation of the copulatory apparatus. or He CO bo Trans. S. Afr Phil. Soc.Vol. XVII. Plate XV. pili ays 1 ' ‘ ? 1 t rw? # oe: Ait Poe eS ~ West, Newman chromo. (151) NEW FORMS OF THE HEMICHORDATA FROM SOUTH AFRICA, I. PHORONOPSIS ALBOMACULATA, g. et Sp. n. II. PHORONIS CAPENSIS, sp. 0. III. PrycHoDERA CAPENSIS, sp. 0. By J: De if. (Grmcurisr, NEAL Y D.Sc. Ph.D... C.M-ZA:S., Government Biologist to the Colony of the Cape of Good Hope. (With Plates XVI., XVII.) (Read June 26, 1907.) INTRODUCTION. The three orders of the Hemichordata* prove to be represented in South Africa: the Enteropneusta by the form here described ; the Pterobranchia by a new species of Cephalodiscus |; and the Phoronidea by the two forms mentioned above. A species of Phoronis is not uncommon in South African seas, and individual specimens are readily obtained in limestone and amongst incrustations of Polyzoa and worm tubes dredged from shallow water (15 to 30 fathoms). A number of the animals were, however, obtained in a much simpler way. About the beginning of May, 1906, numerous specimens were observed in a tank at the Government Marine Laboratory, and there is evidence that they had been brought in with the supply water as larval forms. They were first seen in a small piece of limestone which had been procured from a depth of about 20 fathoms in False Bay some time previously, and it was thought that they had been brought in with the stone. Further search, however, in the tank resulted in the discovery of other * Adopting for the present purpose Harmer’s subdivisions of this group (vide ‘“Cambridge Natural History,” vol. vii.). + Vide ‘‘ Marine Investigations in South Africa,” vol. iv., pp. 173-192. 152 Marine Investigations in South Africa. Vol. V. individuals, one in a large limestone rock which had been for some months out of water before being used to form part of the rock-work in the tank, three in a small piece of stone at the further end of the same tank introduced later, and a solitary specimen in another tank. Further evidence was afforded by the fact that a dried piece of lime- stone put into the tank for the purpose of confirmation had at least one Phoronis on it about eight months afterwards. During the examination of the specimens in the limestone a single specimen (A) was observed which appeared to be a different species, being larger, of a somewhat: different form, and pigmented. This was the only one of its kind then found, and special care was taken to observe its habits and behaviour in the living condition before preserving it for more detailed examination. It appeared to be thriving and specially active, and it was disappointing to find, on proceeding to examine it again, that this unique specimen had entirely disappeared, leaving only the end of the tube visible. After a time, however, the headless trunk of the animal was slowly protruded, and a month later the head region had apparently grown to its former dimensions. Fig. 2 is from a photograph of the animal at this time. Only two other specimens (B and C) of this species have as yet been procured, but it will probably be found that the animal is not so rare as would seem to be indicated. With regard to the first species (Phoronis capensis, sp. n.), there is little of special interest; but as the specimens, on account of their hardiness and their thriving so well in captivity in spite of somewhat severe handling, afforded excellent material for observation of their habits and certain features of the living animal, an opportunity was taken to add a few details to the little that is known on these points. Fig. 1 represents one of this species carrying eggs, and is from the living animal. The second species is of more interest structurally. It shows an apparent advance on species hitherto described in the circum- cesophageal nerve ring being partially sunk in an involution of the epithelium of the body, the single nerve chord being well developed, the nephridia somewhat modified, the longitudinal muscles of the body increased in number, and ova deposited in gelatinous mass in the tube instead of in the tentacles. These distinctive features, especially the first, seemed to neces- sitate the separation of this form from others as a new genus— Phoronopsis. The following description of this animal is necessarily somewhat incomplete on account of the limited material available, but I hope Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 153 to procure additional specimens to check and supplement it. Transverse sections were made of specimen A and longitudinal sections of B. I.—PHORONOPSIS ALBOMACULATA. (Plate XVI., fig. 2.) PHORONOPSIS, g. n. The body is asymmetrical, muscles of body being numerous and more developed on left side, one nerve chord well developed, and nerve ring in an involution of the epidermis, ova deposited in gelatinous mass in the tube. In all the species of Phoronis hitherto described the body is symmetrical or asymmetrical, as indicated by the development of the muscles and nerve of the left side; the muscles of the body are markedly less in number than in Phoronopsis, and there is no trace of any involution of the epidermis at the nerve ring; the ova and larvee are lodged in the coils of the lophophore.* There seems little doubt of the necessity of separating this form from those hitherto described. PHORONOPSIS ALBOMACULATA, sp. n. Size.—The length of the animal removed from its tube was 18 mm., the diameter of the body 1 mm. immediately below the lophophore and 2 mm. at a distance of 4 mm. from the opposite extremity. The diameter of the lophophore from tip to tip of tentacles, when the animal was alive and completely expanded, was 7°5 mm. Tube.—The tube is larger than that of P. capensis, being 1-2 mm. in diameter. It is not embedded—i.e., it does not penetrate the substratum, but rather lies on it, being firmly attached by one side. The substance of the tube spreads over the substratum on the attached side, so that in sections it does not appear circular, but is flattened on one side. The tube is about 30 mm. long, and, in the specimens, was irregu- larly curved, so that the two ends lay near each other. Its substance was apparently of the same nature as that of P. capensis, but firmer and of a much tougher consistency. It was covered by grains of sand and pieces of shell arranged in no definite manner. * Longchamps (8) observed the eggs of Phoronis Miilleri being discharged directly into the water, and suggests that this may be normal. 154 Marine Investigations iw South Africa. Vol. V. Colour.—A pure white pigment of finely branching chromatophores occurs in spots irregularly placed on the tentacles. These spots were somewhat elongate in the direction of the length of the tentacles. To the naked eye each appears as a solid spot, but when examined with a lens is seen to be more or less divided longitudinally, and to consist in reality of two patches, one on each side of the tentacle. At the base of the tentacle they are more numerous, and form a continuous line along the lophophore near the oral region so as to form an incomplete circle. At the median point (that is, the mouth region) a strip of pigment passes backwards towards the anus (or along the dorsal aspect of the animal), and ends in a slightly enlarged circular patch. Whether or not this spot coincides with the anus, as it appears to do, could not with certainty be made out as the pigment was not visible in sections. The white pigment extends on to the body in few and irregular streaks below the lophophore. Apart from this pigment the tentacle and lophophore were clear, transparent, and apparently colourless. The body, however, was of a faint yellowish colour. Nervous System.—The single nerve along the left side of the body is well developed. The nerve cells are numerous and well developed, and are arranged so as to form asolid rod (cf. Caldwell (8), Cori (4), Longchamps (8). A transverse section showed that this nerve is not hollow, the centre being occupied by a clear, refractile, non- staining substance. The nerve was thus, as a whole, partly differentiated from the epithelium, but not sinking away from it. In following the sections upwards however it is seen that as they approach the duct of the nephridia the nerve gradually leaves the epithelium of the body, and when the duct (double, as it is here in the form of a loop) is cut the nerve is seen internal to it. Succeed- ing sections show that, after the nerve has thus passed over the duct on the inside, it again passes out between the two limbs of the duct before joining the circum-cesophageal ring of nerve tissue ; in other words, on coming to the nephridial duct it passes over it on the inside in place of continuing on the outside, where the epidermis of the body is. This twisting of the lateral nerve may be associated with the marked distortion of the body. The anus, at one time terminal, has come to lie near and behind the mouth. The nephridial opening, at one time probably ventral and below the lateral nerve chord, has been carried upwards, necessarily passing ~ over the lateral nerve chord, and finally attains a position near the anus. The passing of the opening of the nephridial duct over the nerve Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 155 may also be associated with its separation from the epidermis at this point. The most striking feature of the nervous system, however, is to be found in the character and position of the nerve ring. It is sunk in a comparatively deep involution of the epidermis, which is so intimately connected with the nervous system that it is most con- veniently dealt with here. This involution or fold of the epidermis passes from the oral side of the animal round on each side, follow- ing the course of the nerve ring, till, on reaching the lophophoral Opening, in or near which are situated the anal and nephridial apertures, it is continued round the body, passing outside these organs. The fold can readily be seen with a low magnifying glass. It varies greatly in depth ; outside the anus it is a mere ridge; it is deepest at the sides of the body, being about one-fourth of its diameter. Anteriorly, z.e., in the oral region, it becomes somewhat shallower. The general character of the histological elements of this fold is indicated in fig. 4. The external part is identical in structure with the general epithelium of the body—a layer of deep epithelium cells, including glandular cells. Towards the tip of the fold, however, these cells become smaller and lower, and at the tip somewhat abruptly change in character and become low, square, with com- paratively large, round nuclei, and without distinct cell demarcations. These are continued down to the bottom of the fold, where they once more abruptly change into deep elongate cells, with punctated nerve substance. The nervous epithelium of the nerve ring does not, therefore, participate in the folding. In some sections of the fold a few cells occur between the cubical epithelium and the epidermis, and apparently a space which is not coelomic. The existence of a space is doubtful, however, and may be an artifact. In life, the small cubical epithelium of the fold is applied to the nervous epithelium, the lip of the folding not standing out as shown in the figure, which is from a specimen (B) killed and fixed in sublimate. In the other specimen (A), which was treated in practi- cally the same way (fixed in sublimate with 1 per cent. acetic acid) before removal from the tube, the lip of the fold was closely applied to the body, The epithelium of the nerve ring is not entirely covered by the fold, even when closely applied to it. In the region of the organs, which for want of a better name I have called “ olfactory organs,” it extends beyond the fold and is freely exposed. The nerve ring is 156 Marine Investigations in South Africa. Vol.. V. therefore elongated, or broadened upwards towards the tentacles here, and, in the same region, elongated downwards in the lateral folds. This downward elongation comes in close approximation to the nephridia, as shown in fig. 5, which is a transverse section of specimen A. With regard to the interpretation of this organ, the most obvious suggestion is that it is of the nature of an introvert, such as occurs in the Polyzoa and Sipunculoidea, and, if so, it might form another link between the Phoronidea and these groups. It seems probable from its size, structure, apparent absence of retractor muscles, and intimate relation with nerve ring, that it does not however act, to any great extent at least, as an organ for the withdrawal of the body, or any part of it—a function which is most efficiently performed by the numerous and powerful muscles of the body. In specimen A we are dealing with a regenerated head, not mpossibly in B also, and it might be suggested that the fold is a stage in the complete separation of the nerve ring from the epi- dermis—a condition which might occur in a completely developed specimen, though the nature of the folding does not seem to sup- port such a view. If any phylogenetic significance is to be attached to the form of this organ, which is possible, it may be that it is the remnant of an ancestral introvert which has been retained with the new function of protection of the nerve ring. Muscles.—The longitudinal muscles of the body were numerous and well developed, especially on the left side. In the region just below the nephridia there were 32 in the left oral chamber, 30 in the right, 18 in the left anal chamber, and 14 in the right, or, according 9 Ist Lophophoral Organ.—In specimen A this organ was not present but in specimen B it was very marked, being a deeply staining mass of glandular cells. Tentacles—The tentacles were numerous—126 in specimen A. They were a little over 3 mm. in length, and ‘08 mm. in diameter. Septa.—The septa seemed to be of the usual number and disposition. The transverse septum was in part without basement tissue. In median longitudinal sections there appeared an off- shoot towards the epistome—a condition which requires further examination and confirmation on other specimens. Nephridia.—The two nephridial tubes are well developed, and in preserved material were bent on themselves, forming a loop, the limbs of which appeared of about equal length. As described above, the nephridial tube of the left side passes between the nerve and the to Longchamps’ formula, Being Transactions of the S. Afr. Phil. Society. Vol. XVII, 10% external epithelial layer of the body. Internally the nephridia opened in the lateral mesenteries, there being two very marked and wide openings to each. These openings were composed of deeply staining masses of cells, which extended up on to the transverse septum. They were not, as in other species, continued down on the lateral mesenteries. Ova.—Specimen C was in all respects like in general form and colour to A and B, so far as could be ascertained by microscopic examination of the living animal protruding from its tube. There were no eggs or embryos in the tentacles, but, on one occasion, when the animal was retracted, a large number of ova were seen lining the mouth of the tube, and these were held together by a gela- tinous substance. The eggs were slightly yellow in colour and ‘1mm. in diameter. They were all in a very early stage of de- velopment. Both the animal and eggs were torn off, probably by a fish or other animal in the tank, only a part of the animal and tube being left, so that later stages of the eggs were not observed. II.—_PHORONIS CAPENSIS, sp. n. (Plate XVI., fig. 1.) There are no satisfactory features by which the various forms, which are here included under the genus Phoronis, to which this species belongs, may be separated from each other, and the description of a supposed new species cannot be drawn up on very definite lines, but rather with a view to affording details, some of which may subsequently be found to be of systematic value. Such particulars are size, form, colour, number of tentacles, tube, number and development of longitudinal muscles, nerve chord, &c. Size, dc.—The body of this species is neither particularly large nor small. The largest specimen was not more than | mm. in diameter at the end of the body immediately below the lophophore. This might be reduced to about half this diameter when the animal was fully extended from its tube. The total length of a specimen removed from its tube was 21 mm., the smallest diameter of its body 1 mm., and the greatest 1:3 mm. (near the basal end), The living animal is clear, colourless, almost transparent. The tube in which it lives is circular and of a brown, horny-like sub- stance, not easily ruptured, and is not confined to any special substratum, but may occur embedded in limestone or between any 158 Marine Investigations in South Africa. Vol. V. calcareous tubes of other animals, even among calcareous alge. (See below for further details.) Nervous System.—This is essentially as described in some other species. There are two very fine tracts of punctated nervous tissue running along each side of the body where it is joined by the lateral septa. Beneath these, on or in the basement membrane, could be detected a very fine tube, such as has been described. No nervous tissue was found anywhere separated from the epidermis. The specially developed patches of nerve tissue at the base of the lophophore were present as described by Benham (2) for P. australis, and, for reasons stated further on, are perhaps to be considered as olfactory organs. Another patch of nervous tissue, apparently representing a sen- sory organ, was found at the base of the epithelium of the floor of the mouth where it joins the transverse septum. The tissue is less developed and definite than in the previous case, but, taken in conjunction with the observations below, it would seem to be an organ of taste, or at least of discrimination of food particles, o which there is a very definite selection and rejection (fig. 6 ne’). Musculature.—The longitudinal muscles of the body are fairly well developed. Near the nephridial region they are symmetrical, that is, an equal number on the right and left of the median septum. According to the convenient formula of Longchamps they would be 12/12 qq, that is, 12 in the right and left anterior chamber, and 4 in the right and left posterior. This, however, was not constant, and 12/11 ee AC vies and other combinations were observed. Lophophoral Organ—This organ in P. capensis appears to be essentially similar to that in other described species. In view of the observations on this organ in the living animal, two parts are to be distinguished. First, the glandular epithelium at the base of the lophophore below the tentacles forming the lower part of the brood chamber. This glandular epithelium extends up on the inner side of one or two of the tentacles, that is, into the region where the more developed embryos lie. It is readily seen in sections that the mucus from the epithelium envelops the eggs, and the mucus with which the mass of developing eggs and embryos are held together is very apparently from this source. Secondly, a free continuation of the epithelium out from the lophophore. The cells here assume rather the characteristic of ordinary epithelium (ciliated). Though in sections little more than a slight projection or fold, this part in the living animal is broad and leaf- Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 159 like, and functions as an organ for conveying the eggs from the nephridial opening to the brood chamber as described below. Tentacles.—The number of tentacles in specimens with eggs, and therefore probably full grown, is about 90, though much fewer were observed in others with rejuvenating (?) heads and in small specimens. The number of coils of the lophophore when contracted (in sections) was at most one and a half on each side, and, when fully extended, one, that is, in the circle of tentacles, the course from a point in front of the middle of the mouth to a corresponding point behind, was about circular with a slight re-entering curve in which the eggs were lodged (vide fig. 1). The coils were flat, that is, not in a turreted form as described in P. australis (2) and P. buskw (7). Septa.—A transverse septum exists in P. capensis, but it is not of the same character as in P. australis (2). In the latter it is com- posed of a homogeneous dense matrix with embedded cells and spaces lined by cells. This condition, which I have also found in section of P. hippocrepra, may have been brought about by the invasion of the septum by the gelatinous basement membrane of the body wall. In P. capensis only a part on each side and behind is so invaded, the rest of the septum being composed of the closely applied coelomic epithelium of the supra- and infra-septal cavities, so that in longitudinal section near the right or left body wall the septum appears of the character found in P. australis, while in a median longitudinal section the septum is in the form of cells with- out basement tissue. The characteristics of the septum in this respect would probably be of value in specific determination, but it has not been described for most species. The mesenteries of the cavity below the transverse septum are of the same character. Gaps, however, occur in them, and the two layers are not always evident. In the nephridial region of the lateral septa the basement tissue, however, appears. Nephridia.—There are two nephridia. In addition to the large opening into the rectal chamber, there is a smaller into the lateral chamber. The rectal opening is continued down the mesentery for a considerable distance, as described in P. australis, and other species. Circulatory System.—Some of the details of the course of circula- tion were made out by examination of sections, but chiefly by observations on the living animal. They showed that the circulation was apparently different from that of P. australis (2). ~ In sections, the afferent vessel was seen to be divided into two 160 Marine Investigations in South Africa. Vol. V. branches, but these do not pass into ‘ circular’ vessels only, but lead by a large vessel (often swollen up into a large cavity full of blood corpuscles) directly into the two branches of the efferent vessel, so as to effect a direct communication between afferent and efferent vessels. This was confirmed by observation on the circulation in the living animal as given below, where the circulation is more fully discussed. Affinities of P. capensis.—The species seem nearest to P. hippocrepia. It differs from specimens of this species which I have examined in the structure of the transverse septa, as already indicated, and in the number of tentacles. The latter characteristic is, however, very variable, and the value of the former as a specific characteristic is not yet proved, and it is by no means certain that the forms are distinct. . The wide geographical separation of the species can reasonably be accounted for by the habits and modes of occurrence of the animals as here described. If they can be conveyed through a pump, along pipe, with a fall of about a foot into a tank of water, and become affixed to a stone, it is more than probable that they will lodge in the material which accumulates on ships’ bottoms, or floating pieces of wood, and be carried great distances in this way. OBSERVATIONS ON BEHAVIOUR AND HABiTs OF PHORONIS CAPENSIS. There is still some considerable doubt on many points connected with the general habits and certain physiological phenomena of Phoronis. Its formation of what might be called ‘‘ pseudo-colonies,”’ in which there is apparently no co-operation or advantage to its individual members ; how the animal apparently penetrates solid limestone ; how the tube is formed ; how food is ingested ; function of the ‘‘lophophoral organ’’ and of epistome; nature of sense organs, if any ; whether the movement of the blood is real circula- tion or merely oscillation—these and other points still remain somewhat obscure. The following notes are based on observations for a year on a “colony,” and on specimens occasionally procured by dredging, and also on repeated observations made under the microscope on speci- mens living in as normal conditions as possible. For convenience, T have arranged these under the following heads :— (a) Mode of occurrence, formation of tube, boring (?), colony formation. (b) Tentacles, muscular and ciliary movements. Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 161 (c) Eggs, larvee, oviposition, breeding season. (d) Lophophoral organ, lophophoral gap, epistome. (e) Sensory organs. (f) Circulation. (a) Mode of Occurrence, Formation of Tube, &c.—Most of the animals examined were found in a limestone of recent origin which occurs on the shore and on the sea-bottom in False Bay. It con- tains a large quantity of rounded sand-grains embedded in a calcareous matrix, which is made up of recent shells. It is bored through by worms, lamellibranchs, and sponges. It seemed at first pretty conclusive that the Phoronis had bored into this lime- stone, as, in most of the cases, where they were chiselled out or the limestone broken, they were found to fit closely the cavities in which they lay, and as the tubes were coated on their out- side with a layer of sand-grains apparently pushed aside when the limestone itself was dissolved. The presence, however, of numerous sponge spicules in this coating of the tube seemed to indicate that the cavity had originally been made by a sponge. Further, the fact that other specimens were found in the interstices of Polyzoa and worm tubes, in one case in the tube of a Serpula which had left or been ejected, and in another case in the loculi of the base of a barnacle shell, is evidence in the same direction. I may add also that no acid reaction was obtained from living specimens. On the whole, the balance of evidence seemed to indicate that this Phoronis is not a limestone-boring animal, and that colony formation, which, however, is not a very characteristic feature of this species, is merely due to local conditions favouring srowth at a particular point. The part of the tube projecting from the material in which the animal occurred varies much in length, being usually about 4 to 6 mm., but sometimes much longer, or entirely absent. This part of the tube was very flexible, and covered with a substance similar to that of its surroundings. The stone was found to be covered with a greyish coating of débris, held together by a sticky substance. On one or two occasions large starfish, which were in the tank, were observed to remain for some time in the stone and clear off this coating without, however, injuring the Phoronis. It would appear that this coating may be produced by the action of the Phoronis themselves. Sections of the projecting part of the tube showed that the débris was not only adherent to the outside of the tube, but was included in the substance of the tube itself. For the probable origin of this mucous substance and particles, see below. In some species the foreign substance adhering to the tube has been described as the ‘ 11 162 Marine Investigations in South Africa. Vol. V. excreta of the animal. In this species the excreta were observed to be ejected in long, solid, cylindrical masses, falling clear of the animal and tube. Growing on the tube were often to be observed solitary stalked Protozoa with horseshoe-shaped nucleus. The exposed part of the tube was readily injured, and occasionally individuals were seen protruding through an aperture in the injured tube. The substance of the tube was semi-transparent, brownish, and of a tough consistency where embedded; in this region there were no inclusions in the substance of the tube. There was evidence that the tube is secreted by glandular epithelium of the body gene- rally. Thus, if the animal is removed from the tube, there is an active secretion of mucus, which soon causes the body to be covered with any loose particles that may be in the neighbourhood. In one case a fairly large active copepod was observed to become entangled in the viscid secretion, and was soon rendered quite helpless. The mucus is at first clear and transparent, but soon becomes whitish and opaque. None of the tubes were straight, but had a more or less irregular curve, sometimes even forming a loop. When tubes were removed from the limestone by decalcifying, they were found to be densely coated with firmly adherent quartz grains, not arranged in any definite manner. These sometimes deeply indented the substance of the tube and the body of the animal. The posterior end of the animal apparently exercises some penetrating though not boring function. The body of the animal varied much in diameter according to the extent to which it was protruded. Under certain conditions, which could not exactly be determined, the animals were greatly extended from the tube. The body and tentacles were then mostly rigidly extended. They sometimes slowly rotated in themselves—both lophophore and body—but did not, as described for some species, bend or wave from side to side. This latter movement was some- times observed, however, when the animals were under observation in small vessels, especially when being examined by transmitted light. Tentacles, Muscular and Ciliary Movement, dc.—The method at first adopted in microscopic examination of the living animals was to remove it from its tube by cutting away the limestone, or to suddenly cut off a protruded head, when after a time it often again expanded fully. The tentacles were then observed to be well pro- vided with long cilia (about one-fourth the diameter of the tentacles). In these cases, however, the cilia were never observed to be in motion Being Transactions of the S. Afr. Phil. Society. Vol. XVIT. 163 (cf. van Beneden’s observations (2), in which he describes the cilia as non-motile). Other observations were then made on animals projecting over the edge of the stone so that transmitted light could be used, In this case the cilia were observed to be very active, though, if the animal were disturbed, they suddenly ceased before the animal withdrew into the tube. On one or two occasions the cilia were observed to remain at rest when the undisturbed animal was fully extended. Expansion of the lophophore was not as described in some species, viz., after the extension of the body, but the tentacles began to spread out at the very commencement of the protrusion. The currents of water were best observed under the microscope. It was found that what might be called the inset current, as is to be expected, was into the space between the outer and inner circle. Particles in suspension in the water were carried into this region even from a distance equal to the length of the outstretched tentacles. The particles, especially the larger, were carried to the mouth on the tentacles, evidently by the active cilia. It was surprising, however, to find that in many cases, after reaching the base of the tentacles or margin of the mouth region, the same particles were returned on the same tentacles, and travelled as rapidly in the opposite direction to the distal end of the tentacle. The tip of the tentacle was then slowly bent backwards, and the particle dropped off on to the stone, the cilia at this part of the tentacle during the process ceasing all movement. In such cases- the particle was observed to have a coating of mucus, by a thread of which it often hung on to the tentacle for a time. In a few cases the particles were dropped off in the same way without first travellmg to the mouth. This was observed to occur not only in the outer circle of tentacles, but also in the inner, in which case they were dropped into the centre of the inner circle when there was a constant and very strong current passing upwards and away from the animal. The disposal of par- ticles in this way seemed as much a function of the cilia as the conveying of them to the mouth. I at first supposed that it was effected by a reversal of the movement of the cilia, but this was never observed. It was afterwards observed, however, that if a tentacle be carefully examined, looking towards it from the direction of the mouth region, the cilia on each side showed the ciliary movement in opposite directions.* This occurred on all the tentacles, both those of the inner and outer row. The apparent movement may best be described as upwards on the left side and downwards on the right of * I do not know whether such ciliary motion has been recorded in any of the Polyzoa, but I have observed it in some. 164 Marine Investigations in South Africa. Vol. V. each tentacle when it is viewed from the oral side of the animal and with the lophophore fully expanded. The result would be, of course, that particles, in contact with the one side only, would be carried in a direction outwards or inwards, and opposite to that of the apparent motion of the cilia (due, of course, to the slower stroke in that direction). The cilia on either side could be brought into contact with the particles by rotation of the tentacle, which was observed in a few cases to occur, but this point was not conclusively established, as exact observations are not here easily made. It is certain, how- ever, that the propulsive action of the cilia is not only towards the mouth, as has been supposed, but is largely concerned in carrying away any rejected particles. Particles of a diameter about equal to a sixth of that of the tentacle, and larger, are carried off in this way, as are also irregular masses of débris that may be caught up in the inhalent current. Smaller particles are got rid of in another way. If an actively feeding animal be viewed laterally, so that the outer and basal part of the tentacles is seen, a large number of particles is observed to be escaping between the bases of the tentacles over the edge of the ‘‘membrane’”’ connecting them, and then to fall in a con- tinuous shower on to the edge of the tube, to which some were observed to adhere (probably the origin of the inclusion seen in the substance of the protruding part of the tube). Another and different action of the tentacles was observed when the animal was feeding actively. This was a sudden bending in towards the mouth of the distal free end of the tentacle both of the inner and outer row (cf. fig. 1, in which one tentacle of the outer row shows the nature of this bending). Single tentacles, indepen- dently of the others immediately next them, showed this movement, which was sharp and definite both in the action and recovery to the normal position. At times this movement was repeated by different tentacles at very short intervals, and in the case of Phoronopsis, in which this movement was more marked, on several occasions it appeared as a quite continuous jaculatory movement all round the lophophore. It might be suggested that the result of this movement is to throw or sweep particles of food towards the mouth, but only in a few instances was this actually seen, and the possibility is not excluded that these cases were accidental. This movement might be compared to the reaction on stimulus of the tentacles of some sea anemones and polyzoa. The inhalent current, which sets in towards the mouth region, passes off in two directions, viz., between the outstretched tentacles of the outer row and downwards, and between the tentacles of the inner row and inwards, where there is formed a very strong current Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 165 upwards, stronger than the inhalent current (being more confined). It might be expected that a part or all of this current would also flow out over the anus and nephridial openings by the large space which forms the open part of the horseshoe-shaped lophophore, and, indeed, Masterman (6), who, however, had not the living animal, describes and figures such a current as existing. If the living animal is carefully observed, however, it can be seen that not only does no such current exist, but that there is a current leading inwards not outwards at this aperture, so that it passes first over the two pillar-like sides of the lophophore which are characterised by the special develop- ment of nervous tissue at this place, then over the nephridial open- ings and the anus, and joins the strong exhalent current of the inner circle of the lophophore. Benham (2) has accurately described this patch of nervous tissue, and regarded it as structurally the only approach to an appearance of a sensory organ in Phoronis, but expresses his doubts on account of its proximity to the excretory openings. The existence of such a current of water however, pass- ing in turn over the nervous epithelium, the renal openings and the anus, removes this objection, and renders the case quite similar to that of the current, for instance, in the palleal chamber of some Mollusca, which passes first over the osphradium, then the renal aperture, and finally the anus. It has been repeatedly observed that the animal seems very sensitive to the condition of the water in which it lives, and I cannot but think that the two special patches of nerve tissue represent a sensory organ similar in function to the osphradium of molluses, and it may be called for want of a better name the olfactory organ. Still another movement may be observed, but with greater diffi- culty. It occurs on the upper part of the body just below the insertion of the lophophore. No current of water was observed, but merely a movement of particles apparently entangled in mucus and in contact with the body. These were slowly carried upwards away from the mouth of the tube. Very small cilia were on occasions observed. This action may account for the fact that no foreign particles, such as might fall into the tube, were found included in its substance where embedded in the stone. Eggs, Larve, Oviposition, Breeding Season, dc.—The eggs and embryos are very conspicuous, and could be readily observed mostly within the lateral bends of the inner circle of tentacles though occasionally projecting outside these bends. Those nearest the body were apparently held together ky the mucus which is secreted by the glandular part of the lophophoral organ; those near the free ends of the tentacle were further developed, some attached to the 166 Marine Investigations in South Africa. Vol. V. tentacles and still in the delicate egg capsule; others, however, were in some cases observed to have hatched out, and to have reached the stage at which the pre-oral hood and the body formed two approximately equal portions. Some embryos at this stage were observed to exhibit a fairly active opening and closing motion of the two limbs thus forming (pre-oral hood and the body), suggesting that the relatively large development of the hood at this stage may have an important physiological function (respiration? attachment ? nutrition ?). The discharge of the ova from the body and lodgment in the brood chamber can readily be observed. Throughout the whole breeding season of about 11 months eggs could be seen in the particular group under observation at any time, in one or other of the specimens, passing up the body cavity singly or in rows of usually about 6 or 8. If a specimen projecting over the edge of the stone (so as to allow of microscopic examination by transmitted light) be examined, the movement of the eggs upwards in the body can readily be observed. At each expansion of the blood vessel from below upwards the eggs or row of eggs was shifted a little further towards the nephridial opening, and on the contraction and emptying of the blood-vessel they were carried back again, though not so far. No evidence of any slow forward movement, such as might be caused by cilia, was apparent. In a typical case the eggs were observed to pass in this manner from the point in the body where it projected from the tube upwards to the nephridial duct in about 10 minutes. Here they became grouped together, remaining thus for 6 minutes. One of the eggs was then seen assuming an elongate slightly bent form (apparently entering the nephridial tube). It was then observed to travel upwards slowly and at a uniform rate inside the nephridial tube which was closely applied to the base of the lophophore. The nephridial tube was then apparently elongated, its opening being covered by the leaf-like part of the lophophoral organ so that on its escape from the opening of the duct the egg was safely carried upwards to the base of the brood pouch and took its place along with the others. It here again assumed a circular form, 0:22 mm. in diameter. Almost immediately after the discharge of the ovum by one nephridial duct the same process took place by the other duct, and so on alternately till all of the group of ova were discharged (in about 15 minutes). At the upper end of the mass of developing eggs the larva were well advanced. In a larva which was observed escaping no trace of tentacles was seen (cf. Longchamps’ observations (8)). In one or two cases the larve were observed swimming about freely, but Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 167 retained by a bending in of the tips of the tentacles of the inner circle. In the particular group of animals under observation nearly all the individuals carried eggs and larve when first found in the beginning of May. A few had them up to the end of June. On November 10th one specimen was observed to have an egg in the body, and by the 20th of the same month more than 90 per cent. had conspicuous clusters of eggs and larve in the tentacles. The comparatively sudden and simultaneous appearance of these was somewhat striking. Soon all of the specimens bore eggs and larve, and this continued up to about the beginning of March of the following year, when a few were seen without them. By May 12th none of the group under observation had eggs. In some of the individuals which were more carefully watched a peculiar occurrence, for which I cannot suggest an explanation, was observed. The animal which had remained with body and lophophore with its egg mass fully extended for months, totally disappeared, leaving only the projecting tube. This seemed a confirmation of the suggestion of the annual dying off of the Phoronis. A few days (8-10) afterwards, however, the same animal was observed projecting (to a less extent) from the tube, but the lophophore was much smaller, the tentacles being only about two- thirds their former length and without eggs. Lophophoral Organ, Lophophoral Gap, Epistome.-—From the observations just described on the method of discharge of ova, it is apparent that the projecting leaf-like fold of the lophophoral organ acts in such a way as to form a closed passage from the aperture of the nephridial duct to the brood cavity, the glandular part supplying the mucus in which the eggs are enveloped and bound together. The whole organ might be described, therefore, as a glandular oviducal furrow. Contrary to what has been observed in other species, I have not found this organ absent in any specimen with eggs, though sections of a large number of individuals might show that this is true of P. capensis also, The lophophoral gap between mouth and anus has received a good deal of attention, and there has been some speculation as to its function. It is a very striking opening in the circle of tentacles as seen in sections, but it does not exist as such in the expanded living animal, in which the gap is no larger than the spaces between the tentacles. This will be made clear from fig. 1, which is from the living animal. It seems quite out of the question that the inhalent current of water directed by the 168 Marine Investigations im South Africa. Vol. V. epistome escapes by this ‘‘gap”’ into the inner circle as has been suggested (Masterman (6) ). It is merely the point of origin of the tentacles, which in this region are of all sizes; two sometimes scarcely projecting have been seen at each side touching each other across the ‘‘ gap,’ and follow- ing these 5 or 6 on each side rapidly increasing in length till they join the fully developed tentacles of the inner circle. These smaller tentacles on each side often overlap at their tips, preventing any wide opening between the regions of the inhalent and exhalent currents. The contraction of these small tentacles and of the tissue in the neighbourhood of the gap, along with the approximation of the tentacles in preserved material, doubtless bring about the appearance of a large gap in sections of this region. The epistome could be readily observed in the living animal in certain positions. In contrast to the other organs of the body it showed a constant and active movement. This occurred at its free edge. Observations were, of course, only possible when the lophophore was fully extended. In this condition the epistome was usually held back against the inner circle of tentacles, the mouth being widely open. Occasionally, however, the epistome descended over the mouth, closing or partly closing it. Various suggestions have been made as to its action, directing the currents of water (Masterman (6) ), preventing a direct passage between mouth and anus through the lophophoral gap (Benham (2) ). These, though quite justifiable deductions from a study of sections, do not seem probable in view of what has been noted above with regard to the behaviour of the animal in the living condition. So far as observa- tions went, the function appeared to be the obvious one of closing the mouth, and its lateral extension on each side; it is doubtless also partly sensory. Circulation.—Though the closed vascular system with red blood of Phoronis is one of its most striking characteristics, there is still some doubt as to whether there is actual circulation or merely oscillation of the blood. This is probably to be accounted for by the difficulty in obtaining accurate observation of the course of the blood. Ina recent paper Enriques (5) describes a unique type of circula- tion which he has observed in Phoronis psanimophila. Ue was enabled to examine the circulation microscopically by removing the animal from its tube by a method which he considers would not injure the animal to such an extent as to upset its normal circula- tion. Briefly, his conclusions are that there is an_ oscillatory movement of the blood plasma, and that, during this process, the Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 169 corpuscles accumulate in the distal or lophophoral region, from which they are finally expelled by a strong contraction of the median vessel into the general vascular system, there being thus a circulation of blood corpuscles but not of plasma. I have also observed something similar to this in specimens of P. capensis which have been removed from their tubes, and also similar move- ments in the vascular system of individuals which have thrown off the lophophoral region, with the exception in this case, of course, that the blood corpuscles, while accumulating at the distal or regenerating end, cannot pass off again by a circulatory movement into the system. I cannot but suspect that these interesting phenomena observed by Enriques, are mainly due to injury or irritation produced in removing the animal from its tube, and might be compared from their mechanical aspect at least to clot formation. The method adopted in making the following observations was to select for microscopic examination specimens projecting over the edge of a piece of stone so that they can be examined by transmitted light. The animals sooner or later began to expand, often to a very considerable extent, and an account of their habit of occasionally rotating slowly in the tube, first in one direction then in another, presented different aspects of the vascular system. The method is rather tedious, but probably ensures normal results. | On the first protrusion of the tentacles, the movement of the blood was readily observed in a few, and, in full expansion, blood was seen to course up and down in all the tentacles. The intervals between such pulsation varied much (4—10 seconds). The inflow of the blood into the blood-vessels of the tentacles was slow, and apparently caused by pressure from behind; the outflow was more rapid and apparently caused by contraction of the vessels. The inflow and outflow of blood was never synchronous in all the tentacles, but was irregular, though occasionally a few neighbouring tentacles showed pulsation at the same time. Hach of the blind tentacular vessels opened into a common circular vessel in which the course of the blood was sometimes in one direction, some- times in another. Two such circular vessels were seen lying not far from each other. These were, however, not recipient and distributing vessels such as oceur in P. australis (2), but were merely the single connecting or circular vessels of the inner and outer circle of tentacles. In both, the movement of the blood was to and fro without any regularity. The outer circular vessel was continued round on the oral side, but the inner circle was interrupted at this point thus (). 170 Marine Investigations in South Africa. Vol. V. The blood flowed away from each side of the lophophore, from the right by a vessel which passed round by the oral region and joined that from the left to form the large vessel on the left side of the descending limb of the alimentary canal. In all these there was observed to be an almost continuous stream of blood downwards away from the lophophoral region. As in some other species, the efferent vessel at a little distance from the lophophoral region gives off a number of blind vessels into the body cavity. These were occasionally very distinctly seen in the living animal, and were then observed to be contractile, recelving blood from the main vessel and expelling it exactly as in the case of the tentacular vessels. The tentacular vessels apparently expelled the blood by con- traction. It would be difficult to say if the circular vessels were contractile. The vessels by which the blood leaves the lophophoral region were not contractile (7.e., the vessel on the left side of the alimentary canal and its two branches). The centrally placed vessel between the ascending and descending limbs of the alimentary tract showed, however, a very marked con- traction from below upwards. This was observed to occur, always in the same direction, through the entire course of so much of the vessel as could be seen (sometimes 10 mm.) under normal conditions, without removing the animal from its tube, in which case the move- ment was abnormal. A large volume of blood (corpuscles and plasma) was seen to be thus conveyed to the lophophoral region and to pass to either side by two short branches of the main vessel. Each of these branches opened directly into a vessel which seems capable of great expansion, and is lodged in a cavity of the lopho- phore very apparent in section. The blood passed into the tentacles in its immediate neighbourhood, and to the tentacles further removed by the circular vessels. There was no evidence of any true. circula- tion through the tentacles nor of circular distributing and recipient vessels, the whole of the blood-vessels of the lophophoral region being merely a complex form of the simple blind vascular diverticula seen on the large vessel within the body. The greater part of the stream of blood thus never entered the tentacles, but passed on directly to the two branches of the efferent vessel which joined each other to form the single vessel situated in the left side of the descending limb of the alimentary canal. There was thus a true circulation, the blood being driven forward by a vessel lying over what in Phoronis corresponds to the dorsal aspect of the alimentary canal. On reaching the anterior end it passes by two vessels round the alimentary canal (cf. the ‘“hearts’’ of annelids) which join to. Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 171 gether on the left side (ventral ?) of the alimentary canal to form the efferent vessel. This passes downwards and joins the contractile afferent vessel, by which the blood is again driven through the same circle. Blind diverticula occur in the course of this vascular system, viz., the tentacular vessels, a group of vessels floating freely in the body cavity some distance below these, and finally a number of vessels penetrating the gonads at the other end of the body. The intervals between the contraction of the dorsal vessel were very uniform in any one individual under observation, but varied much in different individuals. In some they were three seconds, in others as much as ten. They appeared also to differ in the same individual at different times. If the movement of the blood be carefully observed in a favourable position of the animal it is found that after each con- traction of the dorsal vessel is completed there is a very slight return of the blood in its upper part, the quantity returned however being infinitesimal as compared to the large volume passed upwards, and it is only in the upper part of the afferent vessel and carried forward again in the next flow. The same thing happens in the commencement of the efferent vessels. This may be expressed more definitely in the time observations in a particular case. Thus in one case the interval between the contraction of the dorsal vessel was ten seconds. In the afferent vessel the flow of blood continued from the first to the sixth second, in the seventh and eighth there was complete contraction and emptying of the vessel (both of corpuscles and plasma), in the ninth and tenth there was a slight return of blood in the upper part of the vessel. The efferent vessel was never without blood corpuscles. A more decided flow began in the second second and lasted till the eighth, and between such intervals there was a slight return. The lumen of the afferent vessel is less than that of the efferent, but the proportions of blood corpuscles to plasma in each seemed the same. The peristaltic contractions of the dorsal vessel were always towards the free or lophophoral end of the animal in normal conditions. In injured or regenerating animals there is an oscillatory or to- and-fro movement of the blood in the afferent and efferent vessels, and often a crowding together of blood corpuscles into patches which remain stationary for a time in the free or distal region of the body. 172 Marine Investigations in South Africa. Vol. V. III._PTYCHODERA CAPENSIS, sp. n. I have from time to time, in shore collecting found specimens of this Hnteropneust chiefly at or near low water, and generally in coarse sand or gravel. It appears to belong to a species not hitherto described, and, in recording its occurrence in this region, I add a brief description of its external features, which I hope to supplement at a later date by anatomical details and a figure of the animal. The length of the specimens procured varied from about 80 to 130 mm. in the normal expanded condition. Individual specimens, of course, varied much at times when disturbed, but when left in fresh sea-water and coarse sand seemed to assume about the same proportion. The relative size of the various regions of the body did not vary much. Even the caudal region, which in other species has been found to vary so greatly, was in these specimens about the same proportionate length, probably owing to the fact that this species does not show the tendency to break up so markedly as in other species. Some imperfect specimens were procured, but they seem to have been injured in the securing of the animals. None of the specimens kept alive or preserved were observed to break up. Proboscis.—The proboscis is of the usual size and shape. It was mostly somewhat longer than broad, egg-shaped, slightly tapering to the anterior end. When prying among the sand and shells, it was somewhat longer and often bent in various directions. A slight notch occasionally appeared on its posterior dorsal surface. In some conditions the longitudinal muscles of the proboscis were seen in distinct bundles. The colour of the proboscis was pale chrome-yellow, uniform, except when this organ was expanded so that the longitudinal muscles appeared as distinct stripes. Collar.—The dimensions of the collar were also normally fairly constant, its length being usually equal to that of the proboscis. Its breadth was slightly less than its length, being narrow in the middle. The free anterior margin was always somewhat folded. This region, which occupied nearly a half of the total length of the collar, was of a paler yellow than'the succeeding part, which was in the form of a narrow ring. This was followed by a thin band of white pigment in the form of a circular streak, a little further back another thin band or yellow streak, and somewhat behind this, where the collar joined the body, another. The collar often showed longitudinal corrugations thicker in the Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 173 middle, but none occurred between the two last-mentioned yellow streaks. No distinct circular furrow was seen in this region in the living animal. . In one living specimen, which happened to have the lip of the collar widely expanded, the two legs of the skeleton were seen lying at an angle of about 50° to each other. In the apex of the angle was observed what appeared to be a small opening—apparently that of the ‘‘ notochord.” Genital Wings.—These were well developed both in length and breadth. Their greatest breadth was at the posterior end of the gills. It was, when spread out, a little over twice the length of the proboscis. The posterior extremity could not be exactly determined, as from this point they gradually diminish in size and lie alongside the hepatic coeca as mere ridges. The place of transition from distinct folds to ridges is about the middle of the hepatic coeca. Here also the brilliantly coloured gonads ended in most specimens. There was, however, no abrupt transition, as in some other species. The free edge of the genital wings are always in contact with each other where they join the collar. They are transparent throughout, in marked contrast to the gonads. Towards the body they meet each other above the intestine behind the gills, and this region is also clear and transparent. A fine genital streak (apertures of the gonads) occurs along the centre of each, and is of a dark reddish colour, the colour of the gonads themselves being a bright yellow. The genital folds usually met each other dorsally over the body, though often folded outwards, so as to expose the gills; their point of origin is the dorso-lateral region of the body. Gulls.—The gill region is comparatively small, being equal to the combined length of the proboscis and collar. This length did not vary in any of the specimens examined. In breadth it was fairly uniform till near the posterior end, when it abruptly tapered off to a point and was often observed to pass under the joined bases of the genital pleure, about one-seventh of its total length being thus hidden. At its widest anterior part it was about half the length of the proboscis. About fifty gill-slits or pores were counted in the deep furrow at each side of the gill. In the living animal the anterior of these were slit-like, being more than twice as long as broad. Towards the posterior part of the gill they became more circular, and the most posterior were almost circular, sometimes square. In preserved specimens all the openings were decidedly elongate. Hepatic Coeca.—These are about sixty in number, and are arranged in pairs. Anteriorly they are less definite and more widely set 174 Marine Investigations in South Africa. Vol. V. apart, about twelve of them being between the genital folds, by which a few of the anterior of the twelve may be hidden. Further back they are normally in pairs, one on each side of the body opposite each other, but in extensions of the body they were often seen to interdigitate, thus alternating on each side. Posteriorly they gradually diminished, the whole length of the hepatic tract being about half the length of the genital ridge, or one-third of the tail region. In colour the hepatic coeca varied considerably, being, however, always dark brown in the central region. Anteriorly and posteriorly they were more or less light in colour, sometimes pinkish. Tal Region.—The tail region was a little over half the total length, and did not vary much in thickness, being about equal to that of the middle of the hepatic region, which was a little over half the diameter of the collar. The most prominent feature was the presence of three lines running along nearly the whole length of the upper surface, the central one of these being the dorsal nerve chord, and one on each side being a thin yellowish streak, which com- menced about the middle of the hepatic region and continued to near the extremity of the tail. In other species in which such streaks are described they are situated in a groove which passes through the ‘‘islet’’ like cross-bands of glandular tissue. Here, however, these bands pass over them so that epidermal furrows were absent on the dorsal surface, one of the most distinctive external characteristics of this species. On the ventral side the yellowish ventral nerve chord occurs, and interrupts the glandular patch throughout its whole course from the collar to the anus; in contrast to the dorsal nerve it thus lies in an epidermal groove. On the dorsal side of the tail these glandular patches of the epidermis are of no great length transversely to the body, but on the ventral side they appear almost like annulations. SUMMARY. (1) Phronopsis, a new genus of the Phoronidea, differing from Phoronis chiefly in having an involution of the epidermis with definitely differentiated (cubical) cells. The involution occurs below the nerve ring, which it partly covers ; it passes round the body, encircling the mouth, anus, and nephridial apertures. (2) Phoronis capensis, a new species, closely related to P. hippocrepia. (3) In Phoronis capensis the following observations, some of Being Transactions of the S. Afr. Phil. Society. Vol. XVII. 175 which are probably applicable to other species of Phoronis, have been made :— a. Currents of water with food and other particles pass in between the outer and inner circle of tentacles towards the mouth. They pass out between the expanded tentacles, downwards between those of the outer row, and inwards and upwards between those of the inner. b. Another current of water passes in succession over two special patches of nervous epithelium, the nephridial openings and the anal opening, and joins the last-mentioned current. c. Most of the particles in the first current come in contact with the tentacles, and are carried on them to the mouth region ; some of these are then carried back on the same tentacles on which they came and dropped off. d. The two special patches of nerve tissue on the nerve ring are in a position with regard to currents of water similar to the palleal olfactory organ of Mollusca and probably exercise a similar function. e. The nervous tissue at the commencement of the digestive tract appears from the definite rejection of particles after reaching this region to be an organ for the discrimination of food particles, and may be called an organ of taste. f. The lophophoral gap between mouth and anus is in the living and expanded animal no wider than the spaces between the tentacles, and plays no special part in the passage of currents of water. g. The projecting free part of the lophophoral organ is relatively large and leaf-like in life, and in discharge of ova overlaps the nephridial opening conveying the ovum to the brood cavity in the tentacles. The more glandular part probably supplies the mucus in which ova and embryo are enveloped. The whole organ may be called a glandular oviducal furrow. h. The blood (corpuscles and plasma) in the normal condition of the animal passes successively through a median (dorsal?) vessel, two circumcesophageal dilatable vessels, a lateral (ventral ?) vessel, and on again to the median vessel. That is, in these vessels there is a true circulation which, however, becomes oscillatory or partly so under abnormal conditions. i. The movement of the blood is oscillatory (to and fro) in the vascular diverticula of the tentacles, the body cavity and the gonads. It is also oscillatory in the small circular vessel at the base of the tentacles. j. Reproduction may take place throughout the year, but is much more marked in the summer months. k, This species does not die off annually. (4) Ptychodera capensis, a new species of the Enteropneusta. (176) REFERENCES. 1) BenepeN, P. T. Van. Note sur un Annélide céphalobranche sans soies, désigné sous le nom de Crepina. Ann. Sc. Nat. (Zool.) 4¢ série, vol. x., 1858. (2) Bennam, W. B. The Anatomy of Thoronis Australis. Quart. Journ. Micr. Sc., N.S., vol. xxx., 1889. (3) CanpwELL, W. H. Preliminary Note on the Structure, Development, and Affinities of Thoronis. Proc. Roy. Soc., No. 222, 1882. (4) Cort, I. Inaugural Dissertation. Prague, 1889. (5) EnriquEs, P. Atti R. Accad. Lincei, Roma, xiv., 1905. (6) Mastprman, H. On the Diplochorda. Quart. Journ. Mier. Sc., vol. xliii., Part 2, N.S. (7) McIyrosH, W. C. Report on Phoronis Buskii. Challenger Reports, vol. XXVil., 1888. (8) Setys Lonecuamps, M. Ueber Phoronis und Actinotrocha bei Helgoland, Wiss. Meeresunt. Neue folge. Sechster Band. Abteilung Helgoland, Heft 1, EXPLANATION OF PLATES XVI., XVIE. Fic. 1.—Phoronis capensis in nearly complete expansion. The eggs are indicated in the inner circle of tentacles, the jaculatory movement of tentacles by a bent tentacle on the left, the nerve ring by white lines, and the digestive tract by a longitudinal white band. Fia, 2.—Phoronopsis albomaculata, viewed from above (from a photograph of the living animal in complete expansion). Fic. 3.—Longitudinal section of Phoronopsis albomaculata (specimen B), showing fold of epidermis and nerve ring. bl. Blood-vessel. bt. Basement tissue. ep. Epidermis of body. ep’. Modified epidermis of fold. eps. Epistome. it. Tangential section of wall of intestine. do, Lophophoral organ. n. Neryous tissue. meph. Section of duct of nephridium. Fic. 4.—Enlarged view of nerve ring with epidermal fold shown in fig. 3. bt. Basement tissue. coe. Coelomic epithelium. ep, EKpidermis of body. ep’. Modified epidermis of fold. m. Nervous tissue. mneph. Section of duct of nephridium. ts. Transverse septum. Fic. 5.—Transverse section of Phoronopsis albomaculata (specimen A). The section is in reality oblique, as the organs of the left side were at a lower level than those of the right. Figuring as in Fig. 4 with the addition of a. Anus. m. Mouth. mnep’. Cells of internal opening of nephridium. Fic. 6.—Median longitudinal section of Phoronis capensis. 6.t. Basement tissue. eps. Kpistome. m. Mouth. .e. Sub-epidermal nerve tissue of nerve ring. n.e’. Nerve tissue near mouth (organ of taste?). oe. Cisophagus. t. Tentacle. : Mar. lian, 8 JA. Wolk Wale ) Trans. S. Afr. Phil. Soe. Vol. XVII.) , 7 — 6 1‘ i Lp i - = ts i - a! { 7 es . =) 7 i ' i 1 . Lary) ' : e, : i i : - t ij , > a , - j ‘ : A - bs 7 x a Lf a ¢ ’ oe * S y - z 1 ui a a} i n i i : : ; : f a « i =} mee - < = - = - ; IH 1s y - : . t et - - ' 7 i ® 7 x ~ 7 ‘ 7 : ¥ ; >: a. , ‘ 2 " : - i a . »* 7 - | a) . - ~e =: - P : y ’ = | ~ = = q é ' i ' 7 Ul = - : ai - a . - : ‘ pS J ; ac ve — 7 , i — - 7 D - i ‘ i Ps od - — — (Pa i a . ' f = a - : : 4 = . ' 1 7 i 7 ¥ - i ‘ = ae ~ i - - —_ 1 - = 7, : 2 os ' ‘ i a a - I =" = { U : : “ ie a 7 = Sy es = . 7 o ' i 7 7 1 a ee : : - i ‘ pas 7 Y 5 ‘ = ma | iy 7 A 1 wt at - ; m = ae A ‘ “ = \ _ co iS 7: r® i a : = = fl j af - 2 7 a ~ — , ys - bd ' ' - ‘ - _ t - Li s > 1 1 4. 1 . 7 Le ; = * 5 * = > ; ‘ 7 i; ' id - pat =a) bs = 7 ; = = T= xs , wt ie 7 i 2 7. : L fi : 2 : a ' y = 4 5 bs 7 = ‘ ' z - = — 5 : = Tu 7 1 1 ' - 5 fi a : os , ; he 5 id i = rn - oa Y . i b _ 5 a al - > | i a ' =a pa i Aa i _ = = , : ‘ 6 1 q _ ? ren 7 : “ i" ' os ‘ a = : } 7 ‘ - i : = “+ en : 7 ' = 7 = : 7 a oe = fi ‘ ’ = ‘ = i < ' 3 ‘ 7 “ a - Nig = e 7 a ar is 7 = : _ ¥ 7 - i ' ¥ - 7 t a 7 ‘ . ‘ - = : ~ ik 1 : : - : é ‘ a - i 4 = ; - - / 7 7 r - Z 7 TT 4 { s ‘ 4 : - - : ? 7 et] : | iy 7 1 7 ~ 1 ft 7 ——s i - — ' H 7 - : i = < ; - = i nn ‘ : - t t n 4 S re ei £ 7 - f : 7 J : a) . . : a - ie i ‘ a 7 ‘ ¥ hol = ’ T eo i = : 7 u io 7 : _ od — 5 | + ay = - ‘ - - t a a x 4 * : ° i - 4 d 7 ite — i ies ' nl i ‘ UJ i - Las ; = 1 ; = i : 17 1 ~* la ey = < ; P : i 7 - : 1 tS . . - + a a A : 7 “ hes % , , ae y 2 7 : * . = ‘ 7 = ' « * N 7 ; c ; : aU F i a a g : o P 9g i = = ‘, -, - o ; ; s , - 7 ‘ * * = 1 f a 7 7 4, * ; , id r ‘ Mar Inv. S.A. Plate XVII. West,Newman lith. lar) ON A PARASITIC COPEPOD FROM CEHEPHALODISCUS. By W. T. Catman, D.Sc. British Museum (Natural History). (Plates XVIII., XIX.) The parasite dealt with in this paper was discovered by Dr. W. G. Ridewood in the course of his investigation of Cephalo- discus gilchristt from the Cape Seas, and is briefly referred to in his memoir on that species (Mar. Invest. S. Africa, iv., p. 181). At his request I made a preliminary examination of the specimens, and sup- plied him with a few notes, which are incorporated in the paper referred to. In view of the special interest of the host it seemed desirable to attempt a more complete examination of the material, and I gladly avail myself of the opportunity kindly given me by Dr. J. D. F. Gilchrist of publishing a fuller account. Most of the specimens which I have examined were found by Dr. Ridewood in the course of his dissection of the Cephalodiscus, and I am indebted to him for notes on the circumstances of their occurrence. The other specimens were obtained by searching through some pieces of Cephalodiscus-colony which Dr. Ridewood kindly handed over to me for the purpose. The parasite belongs to the family Ascidicolidee, of which most of the members are parasitic in the alimentary canal of Tunicata. The fact, however, that the form to which it is most nearly allied, Enterognathus comatule of Giesbrecht, infests, not a Tunicate, but the Echinoderm Antedon, shows that the nature of the parasite in the present case has not necessarily any bearing on the chordate affinities of its host. In the following account Dr. Giesbrecht’s lucid and detailed description of Hnterognathus* has been taken as a guide. The * Giesbrecht, W., ‘‘ Mitth. ii. Copepoden. 14. Hnterognathus comatule, ein neuer Darmparasit.’’ Mitth. zool. Stat. Neapel, xiv., pp. 61-79, pl. 5, 1900. Dr. 12 178 Marine Investigations in South Africa. Vol. V. characters and affinities of the new genus which I have found it necessary to establish will be discussed later. Faminy ASCIDICOLIDA. ZANCLOPUS* CEPHALODISCI, gen. et. sp. nov. ADULT FEMALE. (Plate XVIII., figs. 1-8.) Total length, 55-62 mm. The body is stout and maggot-shaped, about 34 times as long as wide. The integument is thin and membranous, and the segmenta- tion, especially in the abdominal region, is very obscure. The five thoracic somites are defined by deep constrictions and overlap a little at the sides, but do not form collar-like folds on the dorsal surface as in Hnterognathus. The thoracic limbs, with the exception of the fifth pair, are articulated on the ventral surface of the body, and are almost invisible when the animal is viewed from above. The head is slightly narrowed in front, and there is a blunt, deflexed rostrum, only visible from beneath (fig. 4). Posteriorly the body tapers gradually, without any marked constriction. The genital somite is very short and is obscurely defined from the somites in front and behind. The openings of the oviducts are lateral in position (fig. 6). The copulatory pore was not observed. The following four somites are rather obscurely separated. The furea (fig. 6) is short, the rami not much longer than wide, each terminating in four short spiniform points directed outwards. The antennules and antenne (fig. 4) are short, thick, and not distinctly segmented. The former have each a single terminal seta and a minute seta on the posterior edge. The mouth-cone (fig. 5) is not very prominent. The lower lip has large lateral lobes. The mandibles each end in a scythe-shaped blade projecting between the upper and lower lips. No trace of a mandibular palp could be detected. Immediately behind the mouth-cone on each side is a rounded Giesbrecht has overlooked the fact that Hnterognathus was figured (but not named) many years ago by Prof. W. C. McIntosh (‘‘ Observations on the Marine Zoology of North Uist,” Proc. Roy. Soc. Edinburgh, v., p. 611, fig. 5, 1866. The figure is reproduced in the same author's ‘‘ Marine Invertebrates and Fishes of St. Andrews,” 1875, p. 140). - * From fayk\or, a sickle, and zovce, a foot, in allusion to the sickle-shaped claws on the thoracic feet of the female. Being Transactions of the S. Afr. Phil. Society. Vol, XVII. 179 prominence bearing a single terminal seta (fig. 4, ma’’). A com- parison with Hnterognathus suggests that these prominences probably represent the second maxille. No other mouth-parts appear to be present. The first four pairs of thoracic feet (figs. 7 and 8) are similar in form. The protopodite is more or less distinctly divided into two segments, of which the distal bears externally, in the first three pairs, a fine seta. The basal part of the exopodite is not distinctly defined from the protopodite; it has, on the inner edge, a minute seta which is largest in the third pair and seems to be absent from the fourth. Distally, the exopodite ends in a sickle-shaped claw, at the base of which a small segment can in some cases be detected. The endopodite is apparently unsegmented, and forms a broadly ovate or nearly circular leaflet, bearing four small blunt papille on its distal edge. The feet of the fifth pair (fig. 6) are large ovate plates attached to the side of the body and pointing backwards. ‘[wo very minute setze were observed on the distal margin of each. Mane In FietH Copepopip STAGE. (Plate XIX.) Total length, ‘6 mm. The general shape is Cyclops-like, rather elongated, the greatest breadth being about + of the length. The fifth thoracic somite is distinctly narrower than the fourth. The head is about + of the total length, bluntly pointed in front, with a deflexed rostrum as in the female. The pleura of the head-region are not bent inwards as they are in the adult male of Hnterognathus. The first three somites of the abdomen (fig. 14) diminish successively in length; the fourth is as long as the first, and beneath the cuticle can be seen the division between the fourth and fifth somites of the adult. On the ventral surface of the genital segment are the genital valves (fig. 14, g.v.), each truncate posteriorly and bearing two sete. The fureal rami are longer than in the female and each bears six spines ; the inner spine is set on the dorsal surface, the outer one is minute, and the terminal four, of which the second is the largest, are stout and strongly curved outwards. The antennules (fig. 12, a’) have a very delicate external cuticle which does not seem to show any segmentation proper to this stage, but within which can be seen, in the specimen examined, the seven segments of the succeeding (adult) stage. They are beset with fairly numerous simple hairs but no westhetascs were observed. The 180 Marie Investigations in South Africa. Vol. V. antenne (fig. 13) are composed of three segments and have two, perhaps three, terminal claws. The mouth-cone (fig. 12) with the mandibles (md) and the maxillary prominences ('’) are exactly as in the female, except that the last-named structures seem to have no terminal sete. The first four pairs of feet (figs. 15-17) have the protopodite indistinctly divided into two segments, the distal one bearing, in the first three pairs, a seta on its outer edge. The rami of the first four pairs are each composed of three segments. The distribution of their sete is shown by the following table, drawn up after the plan followed by Dr. Giesbrecht :— Re 1. Re 2. Re 3. | | es | oh : Ist Foot...) 1Se OSi 0 | 2S8e 18t 3Si 0 OSe 1Si | 1Se 3Si 2nd Foot 1Se OSi | 1Se 18i | 2Se 1St 4Si | 0 OSe 28i | 1Se 48i 3rd Foot... 1Se OSi | 1Se 1Si | 2Se 1St 5Si 0 | OSe 28i | 1Se 58i 4th Foot... | 0 | Se OSi | 2Se 1St 58i OSe ISi | OSe 28i | 1Se 4Si The feet of the fifth pair (fig. 14, p®) consist each of two small papillee, of which the inner is the larger, each bearing a single seta. YOUNGER STAGES. Specimens of younger stages were occasionally found, but on account of the very indistinct segmentation of the body and limbs ib was not possible to refer them to the various larval stages recognised in the Copepoda. The youngest stage observed is repre- sented on Plate XVIII., fig. 9. The total length is about -36 mm. The fourth pair of feet are present as bilobed prominences, and the abdomen is divided into two segments. The first three pairs of feet (fig. 10) have both rami in the form of ovate leaflets, the exopodite with four spiniform points on its distal margin ; the second of these points, from the outer side, is larger than the others, and probably represents the single curved claw of the adult female. Mopr oF OccuRRENCE AND PROBABLE LIFE-HISTORY. All the specimens were found in the stomach of adult zooids or nearly full-grown buds. The degree of infection varies in different colonies, or perhaps in different branches of the same colony. In some of the pieces of Cephalodiscus-colony which I examined nearly every adult zooid contained one or more parasites, but in other pieces they were much less abundant. The position generally occupied by the parasite in the stomach of its host is shown in Being Transactions of the S. Afr. Phil. Society. Vol. XVIT, 181 Plate XVIII., fig. 1, but it appears to be a matter of indifference whether the head or the tail is directed towards the anterior end of the stomach. The adult females are most common, and in every case only a single one of these occurs in one host. The eggs were never observed attached to the body, but isolated eggs, or packets of eggs, were sometimes found free in the host’s stomach. The number of eggs deposited at one time appears to vary somewhat. Two packets of two each, two packets of three, and from three to five isolated eggs were observed on different occasions. The diameter of an egg is about 12mm. Of the larval stages, two, three, or four specimens occurred together in one stomach, accompanied or not by an adult female. No adult male was found, and from the analogy of Hnterognathus we may assume that this stage is free- swimming. In several cases it was observed that zooids containing specimens of the parasite had well developed and apparently ripe gonads, so that there would appear to be no “parasitic castration’’ of the host. It is not altogether easy to reconstruct from our observations the probable life-history of the parasite. From the relatively large size of the eggs it may be assumed that hatching takes place at a late stage of development. On two occasions specimens in a stage corresponding to that shown on Plate XVIIL., fig. 9, were found in the act of escaping from a membranous investment which appeared to present no trace of appendages, and was at first regarded as the egg-membrane. The fact that from two to four of these young individuals always occur together seemed also to suggest that they were hatched a situ and had to pass through a free-swimming stage before entering each a separate zooid of the host to become adult females. Further search, however, afforded no evidence of any break in the series of forms, all of them plainly incapable of locomotion, connecting these young stages with the adult. As it seems necessary to assume the existence of a free-swimming stage at some period of the female’s life-history (the male is probably, as already stated, free-swimming when adult) there can be little doubt that the earliest stages observed are preceded, as in Enterognathus, by a free-swimming stage in which the larve pass from one host to another. As in Hnterognathus also, the females probably emerge temporarily from their hosts when sexual maturity is reached in order to be fertilised by the free-swimming males. On again becoming endoparasitic they each select a host which does not already harbour a parasite. 182 Marine Investigations in South Africa. Vol. V. SystTEMATIC PosITION. Although it has not been possible to ascertain some important characters, such as the condition of the copulatory pore in the female, the parasite described above agrees sufficiently well with the definition of the family Ascidicolide as given by Canu,* and resembles with sufficient closeness several types included therein, to leave no doubt that it must be referred to that family. It appears hopeless, in the present state of our knowledge of the parasitic Copepoda, to look for an exact diagnosis either of the family or of its constituent genera. At the same time the new species is so distinct from any of those hitherto described that it appears impossible to avoid the establishment of a new genus for its reception. In the vermiform, or maggot-shaped, body and non-natatory thoracic feet of the female and in the absence of a brood-sac and of maxillipeds it approaches the genera Hnterocola, Aplostoma, Enteropsis, and Hnterognathus. From all of these except the last it is distinguished (in the female sex) by the strongly- hooked exopodites of the first four pairs of thoracic feet. From Enterognathus it differs in the less strongly-marked segmentation of the thoracic region, of which the somites do not overlap dorsally, in the indistinctly segmented appendages, the reduced and palpless mandibles, the vestigial non-prehensile second maxille, and in the absence of the first maxille. In the last-named character it agrees with Aplostoma and Enteropsis, differing from both, however, in the structure of the mandible, second maxilla, and thoracic feet, and in many other details. * Canu, E., ‘“‘ Les Copépodes du Boulonnais.” Trav. Stat. Zool. Wimereux, vi., p. 186, 1892. ae n a 7 | - lal saat ie LAS? 2 at FIG ate, ovosn Jk. 12. 13. 14. 15. 16. IN fe (184 ) EXPLANATION OF THE PLATES. Puate XVIII. Polypide of Cephalodiscus gilchristi, partly dissected to show the position of the parasite Zanclopus cephalodisci in the stomach. One of the gonads of the host is seen immediately above the stomach, . Adult female of Zanclopus cephalodisci, from above. . The same, from the side. The abdomen is generally bent dorsally in the position shown here. . Head of adult female, seen from below. a’, antennule, a’, antenna, ma’’, second maxilla. Between the bases of the antennules is the deflexed rostrum. . The mouth-cone, more highly magnified. L, labrum or upper lip, /, lateral lobe of lower lip, md, mandible. . Abdominal region of adult female, from below; p’, fifth pair of thoracic feet, 0, opening of oviduct. . Thoracic foot of second pair; en, endopodite, ex, exopodite. . Thoracic foot of fourth pair. . Larva of the earliest stage observed. . Third thoracic foot of same; en, endopodite, ex, exopodite. PLATE XIX. Male in fifth Copepodid stage, from above. Appendages omitted. Head of same, from below; a’, antennule, showing through the thin cuticle the segmentation of the adult stage, a’’, antenna, md, mandible, ma’’, second maxilla. Antenna of same. Abdominal region of same, from below ; p°, thoracic foot of fifth pair, g.v., genital valve. First thoracic foot of same; en, endopodite, ex, exopodite. Third thoracic foot. Fourth thoracic foot, Mar. Inv. S.A., Vol. V. \ Plate XVIII. Trans. S. Afr. Phil; Soc., Vol. XVII. Wh ene kee An cen, W. T. Calman, del. ZANCLOPUS CEPHALODISCI. (Female and young), ae _ 7 o. 4 bg "“S Fo ae pbs Mar. Inv. S.A., Vol. V. Bre Pree Ss. Ain Phil Soc, Volt XVIL. DEMS ae W. T. Calman, del. ZANCLOPUS CEPHALODISCI. (Male). (185 ) ON THE GENUS BOTELLINA (Carpenter), WITH A DESCRIPTION OF A NEW SPECIES. By F. Gorpon PEARCEY, Bristol Museum. (Plate XX.) INTRODUCTION. In the year 1869 the late Professor H. P. Carpenter first described what was at that time considered the most interesting and largest known recent arenaceous Rhizopod, measuring | inch (25 mm.) in length, with the diameter of + inch (3 mm.), judging from broken specimens, to which he gave the generic name Botellina, no mention being made of a specific name. Since that time, however, a number of new arenaceous Rhizopods have been discovered fully 14 inches, or more; 7.e., Syringammina fragillissima,* from the Faroe Channel, in a depth of 555 fathoms ; Hyperamnuna palmifornus,+ also from the Farée Channel, in 516 fathoms ; Reophax nodulosa,+ from the Antarctic and Pacific Oceans, in depths from 1,300 to 2,900 fathoms; Pelosina variabilis,§ and others. In 1881 Dr. H. B. Brady redescribed the genus Botellina (from the same fragmentary specimens with which Professor H. P. Carpenter had made his description in 1869), and to which he gave the specific name labyrinthica,|| reproduced and figured in the Challenger Reports, Foraminifera.4’ Botellina labyrinthica, Brady, was first obtained in some abundance at a single station (No. 51) on the third cruise of H.M.S. Porcupine, in 1869, at a point lying on the border- line, between the warm and cold areas of the Farde Channel, at a depth of 440 fathoms, lat. 60° 6’ N., long. 8° 14’ W., bottom tempera- * H. B. Brady, Proc. Roy. Soc., 1883, vol. xxxv., p. 155, pls. 2-3. + F. G. Pearcey, Trans. Nat. Hist. Soc., Glasgow, vol. ii., pt. 2, new series, pl. 3, 1887-8. t H. B. Brady, Chal. Reports Foraminifera, vol. ix., p. 294, pl. 31, figs. 1-9. § Ibid. pp. 235-236, pl. 26, figs. 7-9. || Ibid., Quart. Journ. Mier. Sci., vol. xxi., new series, p. 48, *| Ibid, Chal, Reports, Foraminifera, vol. ix, 186 Marine Investigations in South Africa. Vol. V. ture 42° F., and the surface water 51:°6° F. It was again met with by the Naturalists of the Anight EHrrant and Triton Expeditions in 1880 and 1882, but always in a fragmentary condition in the same areas, at a depth of 516 fathoms in the warm area, and in 580 fathoms in the cold area, with a bottom temperature 46°5 and 31° F. respectively. It would thus appear to be more common in the cold area, where it was taken in the greatest abundance, strongly indicating that it favours a low temperature. In 1886 Mr. Joseph Wright, F.G.S.,* again records B. labyrinthica as having been obtained in considerable abundance in a dredging taken about midway between Belfast Lough and Portpatrick, at a depth of 100 fathoms, and again in September, 1902, from washings of dredged material from Rathlin Sound, Church Bay, in 17 to 24 fathoms, but he makes no mention of the temperature of the water. So far as I am aware, B. labyrinthica has not since been taken or recorded from any other locality. Ten years later (in 1879), after its first discovery, I had the pleasure of examining some of the specimens of B. labyrinthica obtained by the Porcupine Expedition, which I considered at that time were merely fragments of an incomplete species, and mentioned the fact to the late Dr. H. B. Brady, who quite agreed with me. At that time he was preparing the Challenger Report; we also held similar views with regard to other arenaceous forms described and figured in that publication, viz., Rhabdamnuna discreta, Hyperam- mina friabilis, and others, as was proved by the discovery of a new and perfect species of Hyperamnuna (H. palnuformis), figured and described by me from the Farde Channel. } In December, 1904, while occupied, under the direction of Sir John Murray, examining a series of marine deposits collected on board the Cape Government Zoological investigation vessel, ss. Pieter Faure (the late Captain Turbyne), off the N.E. and S.W. coasts of Africa, and in the vicinity of the Agulhas Bank, I observed several fragments of a large arenaceous Foraminifera, which I considered to be closely allied to Professor H. P. Carpenter’s genus Botellina. These samples of deposit had been sent to Sir John Murray direct from the Cape of Good Hope, as they were obtained by dredge, or trawl, and placed in canvas or strong cotton- cloth bags, so that the general character of the samples as a whole * J. Wright, Foraminifera from Rathlin Island, Irish Naturalist, vol. xi., pp. 211-213. + Ibid., second dredging cruise of the ss. Protector. Belfast Nat. Field Club, 1886. t F. G. Pearcey, on the Foraminifera of the Farde Channel, Trans. Nat. Hist. Soc., Glasgow, new series, 1887-8, pp. 163-79, vol. ii., pt. 2, pl. 3. Being Transactions of the S. Afr. Phil. Society. Vol. XVT. 257 could not at the time be made out. On closer examination, later, it was found that several of these samples were made up almost wholly of a beautiful arenaceous Foraminifera of large dimensions, with an erect robust test, and pinnate in form, measuring from 3 inch to 2 inches or more in height, 2 inch to } inch in circumference, varying in colour from a brick-red to light and dark brown, or burnt- sienna, of which in previous samples I had examined I had obtained only small fragments. At two stations, Nos. 593 and 594, lat. 33° 50' S., long. 25° 54’ 30” E. in 26 fathoms, the samples from both of these stations were found to consist of a mass of this gigantic Rhizopod, sufficient to more than fill a half-gallon measure—enough, surely, to gladden the heart of the most ardent Rhizopodist. Here, then, was sufficient material to work out the true character and position of the genus Botellina, of which hitherto fragments only had been discovered. I therefore decided to examine all the samples carefully with that purpose in view. The results of my study are depicted in the following pages. Notwithstanding the large amount of material on hand, there were still serious doubts as to whether all or any of the specimens were really perfect. In the great number afterwards examined, I found that the basal portion of each individual specimen (with three exceptions) showed a true and more or less ciean fracture (see figs. 1, a—b, pl. 1), as if they had been broken sharply off from a basal attachment, showing clearly that they must have been, when living in their natural condition, attached ta some foreign body on the sea-floor, or had possessed a large primordial chamber embedded in the deposit to support such a large test; although diligent search was made nothing of the kind was found, till a sample of deposit obtained off Cape Natal was examined, viz., Station No. 11,074, Cape Natal, N. } W., distant 4} miles, at a depth of 55 fathoms. In this deposit, composed of a siliceous sand, containing a considerable percentage of shell and coral fragments, amongst which a number of the large Botellina were found, seven large oval, sublenticular, and subangular arenaceous chambers were obtained, showing a prominent elongation or tubular neck at one point, similar in composition, character, and colour to the large fractured, robust pinnate form previously discovered, which at once connected them with the incomplete arenaceous tests or Botellina, mentioned above, as taken in mass at Stations Nos. 593 and 594; indeed, with two or three of these chambers it was found possible, with scarce a doubt, to fit the fracture of the neck-like prolongations of these chambers to the fractures at the basal ends of the large pinnate branching 188 Marine Investigations in South Africa, Vol. V. form, thus providing it with a primordial chamber (see Pl. XX., figs. 2-3). And although I have not found a complete or perfect specimen, viz., ‘‘the large pinnate test with a primordial chamber intact,”’ there can be no doubt that these few large cells or chambers, taken in the same haul with the branching tests, of the same characteristic form and composition, their fractured tubular necks fitting as they do, in two or three instances, exactly the broken basal portions of the larger erect branching tests, ave the primordial cells with which they were fixed on the sea-floor, and from which these beautiful erect pinnate structures were produced, as will be seen by the following detailed description, with figures showing fractured and restored specimens (Pl. XX., figs. 1, 2, and 3). Famiry ASTRORHIZIDA. Sup-Famity RHABDAMMININ AL. Genus BOTELLINA, Carpenter. BotEuina, Carpenter (1869). Burscuui, Brady. GENERIC CHARACTERS. TypicaL Form. (Botellina pinnata, Pearcey.) Test free, arenaceous, erect, pinnate, rising from a primordial chamber, oval, subglobular, subangular, or compressed in form, with pseudopodial openings situated at the extremity of pinnate outgrowths; walls thick, of very firm consistence, subdivided into chambers which communicate freely into a main tubular chamber, running through the whole test, compactly cemented and generally smooth externally, in colour ferric brown of various shades. It is conspicuous amongst all other known AsTRORHIZIDE by its robust form and size. PRIMITIVE Form. (Botellina labyrinthica, Brady.) Test arenaceous, cylindrical, straight or slightly curved, some- what irregular in outline, one end rounded and more or less swollen (the natural condition of the other end not certainly known); walls of the test of firm consistence, rough, without external fine cement, subdivided irregularly by a labyrinth of sand-grains cemented Being Transactions of the S. Afr. Phil. Socvety. Vol. XVII. 189 together at various angles forming rude chamberlets which open out into a main tube (or chamber), which runs through nearly the whole test. Incomplete specimens only known. DEFINITION OF NEW SPECIES. Botellina pinnata, sp. nov Test free, erect, arenaceous, comparatively smooth externally, tubular, in the form of a slightly compressed or rounded robust pinnate structure ; the pinnate outgrowths rounded and slightly swollen, compressed or lobulated at their distal ends, with a series of pseudopodial apertures at the apex,—these are covered with a very fine, pale-coloured cement, from which (in the fresh state) numerous delicate transparent spicules project irregularly. Size, 1 to 24 inches (25 to 62 mm.) in height, with a diameter of ,%; to 3 inch (3°5 to 6 mm.) rising from a basal or primordial more or less inflated chamber £ to about 4 inch broad (9 to 12 mm.); oval, subglobular, subangular, or more or less compressed, from which arises a short cone-shaped neck before becoming divided into regular alternate pinnate outgrowths, which at times again divide into radiating branches or offshoots, but always retaining the pinnate character. Walls thick, of very firm consistence, finely cemented externally, and with minute chambers, which communicate into a main tubular passage running through the whole structure opening out freely, vestibular-like, into the pinnate outgrowths. Colour in various shades of red and brown, or ferric-brown. The specimens on which the genus Botellina has been founded differ from all other known AsTRorHIzIDa&, not only on account of its size, but in the general structure of its test, the walls of which are chambered, and therefore represents one of the highest types of structural development among the recent arenaceous Foraminifera. In Botellina pinnata we have a well-defined method of building up the test; the main body of the test is composed of coarse materials. The walls are of firm consistence, ;'5 to 8; of an inch (35 to 10°5 mm.) in thickness, composed of siliceous grains, with a mean diameter of 0°5 mm., made up chiefly of Quartz, Kircon, and a sprinkling of Glawconitic particles, with an occasional Garnet or two, the whole incorporated by a siliceous and ferruginous cement. A thin layer on the exterior is more or less solid and imperforate, giving the whole structure a smooth and solid appearance. The 190 Marine Investigations iu South Africa. Vol. V. siliceous grains are so arranged in building up the wall that they form a network of minute chambers communicating freely with each other, and perforated with tubular-like passages opening out freely into a main central chamber, supplemented and strengthened at intervals by the extension of a portion of the walls into the interior ; in the form of septa, constructed, like the remainder of the test, of cemented sand-grains (Pl. XX., figs. 8, 9). These chambers, having free communication with each other, are generally quite filled with green sarcode, containing nuclear (?) corpuscles. Diameter of the central chamber variable (m. di. .4, inch = 1:26 mm.), internal chitinous lining absent. The pseudopodial apertures are situated at the extreme or peripheral ends of the pinnate outgrowths (see woodcut), formed sometimes of three or Front view of a peripheral end of one of the pinnate outgrowths of Botellina pinata, sp. nov., after it has been treated with dilute hydrochloric acid. Magnified 12 diameters; a, a, pseudopcodial apertures. four transverse slits, or more generally of irregular spaces between the agglutinated sand-grains. These apertures are almost closed in with a light brown cement made up of carbonate of lime and ferru- ginous material, from which extend minute transparent spicules also formed of carbonate of lime, produced to all appearance by the organism itself as a protective agent. These portions are of a much paler colour than any other part of the test, due to a higher percentage of lime at these points than elsewhere, giving a bright and life-like effect to the whole structure. On the test being laid open longitudinally, the main central chamber is seen to start from a large primordial cell, from whence a main passage runs through the whole structure, branching off into Being Transactions of the 8. Afr. Phil. Society. Vol. XVII. 191 vestibular-like passages to the pinnate outgrowths; the septa from the inner walls are exposed, as also the foramina, or tubular com- munications to the wall chambers which open out into it, shown in POX shes 8:90 and Wd, a,b) \e. The same figures show the wall chambers, by means of micro- photography, of the actual specimens, which are not accidental lacunze, but in a measure regularly constructed ; the sand-grains which form their walls are fixed to each other by a siliceous com- pound, and are arranged in a more or less orderly fashion, so as to form a labyrinth of minute chambers. A transverse section across one of the pinnate outgrowths (Pl. XX., fig. 9) magnified twelve diameters shows the wall chambers more clearly. In this figure the thickness of the walls indicated; also the fine thin layer of siliceo-ferruginous cement, d, which contains about 2 per cent. of carbonate of lime, and forms the final outer coating of the walls. The wall of the primordial cell is chambered in a similar manner to that of the remainder of the test (PI. I., fig. 8b). It possesses one large, or from two to five small pseudopodial (?) openings (figs. 1-3 and 7e); oval, or slightly projecting outwards along the edge of its basal portion, which, when living, is most probably buried in the deposit on the sea-floor, and by which means it is enabled to support or anchor the large, erect, robust test. The junction, or neck, connecting the distal portion of the test with the primordial chamber, being the weakest point of the whole structure, will doubtless account for so many imperfect specimens being taken by means of the trawl and dredge, minus the primordial chamber. CONCLUDING REMARKS. Dr. H. B. Brady, in his description of Botellina labyrinthica, gives its specific name evidently on account, as he states, of the interior of the tube being subdivided irregularly by a labyrinth of coarse sandy particles, except at the rounded terminal cavity (?) which forms an undivided chamber. And, later on, he states that the test has the appearance of a cylindrical tube of a somewhat irregular diameter, one end rather swollen and rounded, the other end always imperfect, apparently broken. At the broad end, the investment is thin and incomplete, and there are many orifices (chambers) * left between the sand-grains; and this fact, together with the broken condition of the specimens, gives rise to the supposition that when * The italics are my own. 192 Marine Investigations in South Africa. Vol. V. living the test is erect and sessile, growing attached or rooted by its narrow extremity to some fixed base, and that the interstitial orifice of the terminal chamber serves as the general aperture. It would appear quite evident from the above that the late Dr. Brady was cognisant of the true character of this interesting rhizopod when in its perfect living condition, although no definite mention is made of the chamber walls; it must be borne in mind that he had but incomplete fragmentary specimens to deal with ; the fact that he mentions the many orifices left between the sand-grains, and the interior of the tube (or central chamber)* in parts being sub- divided, is, I take it, an admittance that he saw the primitive arrangement of chambers in the walls of the test. Again, the iate Dr. H. C. Carpenter (loc. cit.) states that the cavity of the tube is not divided into chambers by interposed septa, as in the genus Reophax ; but it is continuous throughout, though traversed in every part of its length by irregular processes, which goes to prove its close affinity to the structure of the chambered walls of Botellina pinnata. Neither Dr. Carpenter nor Dr. Brady mentions any special formation of chambers by the sand-grains in the building up of the walls of the test (except the irregular processes traversing the whole length of the tube (?)), from which it would be inferred that they both saw, at least in some of the fragments examined by them, a central continuous tube, or main chamber in direct communication with the interstices, cellular, or chambered wall structure. I have examined some of the actual specimens or fragments from which Messrs. Carpenter and Brady made their descriptions, and these show definite indications of chambers in the walls of the test, with inter-communications with the main chamber, resembling that of B. pinnata, but the fine material which forms the outer coating and gives the smooth and solid finish to the outer surface of the whole test of Botellina pinnata is altogether wanting in B. labyrinthica ; still, I consider there is sufficient generic similarity to retain the new species under the genus Botellina founded by the late Dr. H. P. Carpenter, although on first acquaintance there is a strong desire to form a new genus, which, however, is lost sight of on structural examination of the tests of each species. I wish here to thank my friend Mr. J. W. Tutcher, of Bristol, for the energetic manner in which he undertook the difficult task of producing by micro-photography figs. 8-11 on the Plate. * The italics are my own. Being Transactions of the S. Afr. Phil. Society. Vol. XVII, 193 List of Srations, witH LOCALITIES, &c., FROM WHICH Botellina pinnata HAVE BEEN OBTAINED. > - ne Ag 3 23 Latitude. Longitude. 3 & General Remarks. 2 os 7, Am el 33° 54’ 13!’ S. | 250 53’ 30’ EB. B. pinnata, moderately common. an 548 580 | 34°1' 30'S. | 25° 45’ 00" E. Two large specimens and fragments. 593 | 33050’ 00’ S. | 259 54’ 30’ E. | B.pinnata,in mass. These two samples and | fully filled a half-gallon measure of B. 594 pinnata alone. In this sample were also obtained a few irregular perforated slabs of agglutinated shelly sand, overgrown with Serpula, Polyzoa, Coral, Hydrozoa, and Foraminifera, Gasteropod, and Lamellibranch shells, shell fragments, and siliceous sand. 781 | 33°53’ 00''S. | 28°12'00" BH. | 45 Quite 2 lbs. in weight of B. pinnata, (Off East | Beacon, with a few Gasteropods, Polyzoa, and a about 17 | miles E. | mass of a large Hydroid (Sestularia ?), of East | London.) sand and shell fragments. The B. pin- nata taken in this haul are of a bright red colour. 805 | 3303/00’ S. | 27°57'00'' BK. | 32 A good many B. pinnata, brown and and bright red in colour. 806 826 | 3606’ 45 S. | 27055’ 45" H. | 43 About 6 lbs. in weight of material, and composed of sandy mud and shells, with 827 hardened lumps of homogeneous mud. B. pinnata moderately common. 1,108 Bird Island | Passage, 10 A few specimens and fragments of B. and Algoa | Bay. to | pinnata, and a number of a smaller 1,109 16 | species, nov. 1,882 Cape St. | Blaize, 125 Several fragments. N. by E., | distant 73 | miles. ; 10,778 Cape | Natal, 85 A few fragments of B. pinnata, with W. 2N., | distant a number of specimens of a smaller 123 | miles. species. Bottom deposit, a coarse sandy mud. 11,074 | Cape Natal, | N. 4 W., 59 This deposit, composed of a dead 44 miles | distant. coarse shelly sand and coral fragments containing a number of ferric-brown phosphatic concretions, among which was found a good number of B. pinnata, and seven large primordial chambers belonging to them, together with many other large foraminifera, as Polytrema rubra, Rupertia sp. nov., Astrorhizasp. ? Cristellaria, &c. . 10,834 Umblote | River 40 A number of highly coloured B. pin- mouth, | N. by | nata, and some fragments of a smaller W. 4 W., | distance species, nov. 84 | miles. : 11,188 § Mouth | of the B. pinnata, in mass. Nearly a quart Umkomaas | River, measure full, many with incrusting N.W. by | W. 4 W., Polyzoa, with a great quantity of a large distant | 5} miles. Hydrozoa (Tubularia? sp. ?), worm tubes, free Polyzoa, Gasteropods, and Lamellibranchs, with a quantity of shelly sand, shingle, and coral fragments. 13 (194 ) EXPLANATION OF PLATE XxX. Botellina pinnata, sp. nov. Fig. 1 . a, Branching form, showing three offshoots from one primordial chamber ; b, primordial chamber detached from the main test by the trawl when captured ; slightly enlarged. The fractured parts, c c, shown in this figure were found to fit each other exactly ; e, pseudopodial (?) apertures. Station 11,074; off Cape Natal; depth, 55 fathoms. 2-3. Typical forms of B. pinata, with primordial chambers restored; the “4 10. abt: pseudopodial apertures are shown armed with delicate spicules; ¢ e, pseudopodial (?) apertures. Station 11,074. . A somewhat compressed form, with double branching of pinnate outgrowths ; primordial chamber broken off from distal portion of test; slightly enlarged. Station 593-594. . A double branching form minus the primordial chamber ; slightly enlarged ; this form of test was found comparatively common. Station 781 ; depth, 45 fathoms. . Specimen from Station 805-806, showing new offshoot from an old fracture of the test ; natural size. . Detached primordial chamber before being ground down to show the interior and wall chambers; natural size ; e, pseudopodial (?) apertures. . Detached primordial chamber (fig. 7), after a portion of one side has been ground away longitudinally; (microphoto) magnified 4 diameters; a, interior of main chamber; b, wall chambers; c, elongated neck showing tubular passage communicating to the upper portion of the main test and pinnate outgrowths ; d, external covering of cement. . Micro-photograph of a transverse section across one of the pinnate out- growths; magnified 12 diameters; a, main passage which forms the direct communication to the primordial chamber; 6 6, septa; c, wall chambers; d, thin layer of cement which forms the outer coating of the test. Micro-photograph of a part longitudinal section of a portion of the test, magnified 4 diameters; a, main passage; b, tubular openings from the wall chambers into main passage; c, wall chambers exposed after external coating of cement has been removed. Micro-photograph of a longitudinal section of two of the pinnate out- growths showing numerous openings from wall chambers; a a, pseudopodial apertures. (See also woodcut, p. 190.) Plate ix. cgi = ahs x tmans. 5. AfrEhil.Soc.Vol. Mar. Inv. S.A.Vol.V. West, Newman lith Ov EeipknaNPAY eNN ACMA Sp mor NITE: albomaculata (Phoronopsis), 151 | capensis (Doridium), 28, 29 amoenula (Idaliella), 66, 80 | o (Doriopsilla), 64 Antedon, 177 | % (Doriopsis), 60 Anaspidea, 2 5 (Geitodoris), 47 aperta (Philine), 24, 26 | 7 (Janolus), go Aplostoma, 182 | 5 (Janus), 89 Aplysia, 2 y (Marsenia), 105 Aplysia allochroa, 4 4 (Nembrotha), 68 5 cirrhifera, 20 | (Philine), 27 » eusiphonata, 9 | a (Ptychodera), 151--172 » gargantua, 5 | ef (Pleurobrancheae), I, 31,-32 > gilehristi, 2 of (Pleurophyllidia), 99 » lobata, 8 ; (Phoronis), 151, 152 5 monochroa., 13 | (Tritonidoxa), 87 » poikilia, to | capucina (Melibe), 96 » sibogae, 13 | catena (Philine), 27 » tongana. 15 | cephalodisci (Zanclopus), 178 » woodi, 12 | Cephalaspidea, 23 Aplvsiella, 19 Cephalodiscus, 151, 177 Aplysiidae, 2 "5 gilchristi, 177 Aplysiidae propriae, 2 | Chelidonura, 29 Archidorididae, 41 Chelidonura aenigmatica, 29 Archidoris capensis, 42 | . amoena, 29 6 granosa, 43 | % hirundinina, 29 scripta, 44 | 6 inermis 29 arrogans (Platydoris), 61 ” philinopsis, 29 Ascidicolidae, 177, 178 | ” plebeia, 29 aspersa (Idaliella), 80 a varians, 29 Astrorhizidae, 188, 189 a velutina, 29 atlanticus (Glaucus) 94 | Chioraera, 95 Atthilidae, 82 | Chromodorididae, 55 aurantiaca (Madrella), go | | Chromodoris, 55, 57 australis (Phoronis), 158, 169 | Chromodoris albolimbata, 55 ms (lanolus) 89 si euelpis, 56 ‘ (Melibe), 96 | comatulae (Enterognathus), 177 Berthella, 39 cirrhifera (Aclesia), 20, 23 Berthella granulata, 40, 41 | 4; (Aplysia), 20 5 bicolor, 45, 46 clavigera (Triopa), 65 bertheloti (Staurodoris), 45, 46 Cleanthus, 39 Botellina, 188-189, 185 coeruleo-pictus (Janus), 89 Botellina labyrinthica, 185, 186, 188, complanata (Geitodoris), 47 IOI compta (Oscaniopsis), 35 Botellina pinnata, 188, 189 cristata (Nembrotha), 71 brunnea (Aphelodoris), 58 | cyaneum (Doridium), 28 bucephala (Melibe), 96 cylindricum (Doridium), 28 Bulla schroeteri, 24 depictum (Doridium, 28 Bullaea, 23 depressa (Staurodoris), 46 buskii (Phoronis), 159 diaphana (Nembrotha), 68 caesia (Doriopsis), 62 Diaulula capensis, 45 californica (Dolabella), 15 5 morosa, 50 callosa (Dolabella), 16 Diaululidae, 48 3 (Doriopsis), 61 diomedeum (Doridium), 28 calva (Staurodoris), 46 Discodorididae, 47 capense (Doridium), 28, 29 discreta (Rhabdammina), 186 capensis (Archidoris), 42 Dolabella, 14 (Diaulula), 48 Dolabella californica, 15 ” 196 Dolabella callosa, 16 Geitodoris, 47 43 elongata, 15 Geitodoris capensis, 47 = ecaudata, 15 ~ complanata, 47 = hasselti, 15, 16 immunda, 47 * hemprichii, 15 gilchristi (Aplysia), 2 a rumphii, 14, 15, 16, 19 4 (Cephalodiscus), 177 =) teremidi, 15 a (Pleurophyllidia), 101, 102 ne tongana, 15 (Planocera), 145 truncata, 15 d’ Orbignyi (Staurodoris), 45 Dorididae er yptobranchiatae, 41 glabella (Doris Gen?), 54 Glaucidae, 94 Glaucus, 04 aS phanerobranchiatae, 65 Glaucus atlanticus, 94 " 28 | Goniodorididae, 79 Doridium, 28 | gracilis (Membrotha), 68 Fa albo-ventrale, 2 | He Glstopa))s.oo .; capense, 28, 29 | granosa (Archidoris), 43 a cyaneum, 28 granulata (Berthella), 40, 41 a cylindricum, 28 9 (Oscaniella), 39 depictum, 28 | granulatus (Pleurobranchus), 1, 37 5 diomedeum, 28 | 40, 41 . gardineri, 2 gratiosa (Nembrotha), 68 55 lineolatum, 28 hasselti (Dolabella), 15, 16 es obscurum, 29 Hemichordata, 151 x ocelligerum, 28 hemprichii (Dolabella), 15 ‘. pilsbryi, 28 hirundinina (Chelidonura), 2 3 punctilucens, 28 | hippocrepia (Phoronis), 159 -f purpureum, 28 | horatii (Pleurophyllidia), 100 reticulatum, 29 hyalinus (lanolus), 89 a tricoloratum, 28 Hyperammina friabilis, 186 Doriopsides, 61 Doriopsididae, 60 Doriopsilla, 64 Ms palmiformis, 185, 186 Idalia, 79 Idalia elegans, 79 Doriopsilla capensis, 64 Doriopsis, 60 Doriopsis, sp, 63 a caesia, 62 3 callosa, 61 capensis, 60 Doris (Gen.?) glabella, 54 ” ” per plexa, 53 i pseudida, 52 ecaudata (Dolabella), 15 Echinospira, 105 edwardsi (Nembrotha), 68 elegans (Idalia). 79 elongata (Dolabella), 15 Enterocola, 182 Enterognathus, 178, 179, I81, 182 Enterognathus comatulae, 177 Enteropsis, 182 » leachii, 80 », mediterranea, 80 5, tentaculata. 80 Idaliella, 80 Idaliella amoenula, 66, 80 5 aspersa, 80 ., inaequalis, 80 5, pulchella, 80 immunda (Geitodoris), 47 impexa (Aclesia), 20 inaequalis (Idaliella), 80 indecora (Tritonia), 85 inermis (Chelidonura), 29 Ianidae, 88 Ianolus, 89 Ianolus australis, 89 » capensis, go » hyalinus, 89 januarii (Staurodoris), 45, 46 Janus capensis, 89 » coeruleo-pictus, 89 5 cristatus, 89 » sanguineus, 89 Enteropneusta, 151 euchroa (Pleurophyllidia), to2 euelpis (Chromodoris ‘, 56 Euplocamus, 70 Euplocamus croceus, 71 | A croceus var. Capensis, 71 | japonicus (Euplocamus), 71 ¥r japonicus, 71 | Kalinga, 74 ; pacificus, 71 | Kalinga ornata, 75 eusiphonata (Aplysia), 9 ferruginosa (Madrella), go kubaryana (Nembrotha), 68 fimbriata (Melibe), 96 | labyrinthica (Bottelina), 185, 188, 191: fragillissima (Syringammina), 185 | leachii (Idalia), 80 friabilis (Hyperamina), 186 | leonina (Melibe), 96 gardineri (Doridium), 2 | leptoconcha (Marsenia), 106 gargantua (Aplysia), 5 | lima (Philine), 27 Kaloplocamus, 70 lineolata (Nembrotha), 68 lineolatum (Doridium), 28 Lobaria, 23 lobata (Aplysia), 8 longicornis (Triopa), 66 loveni (Philine), 27 lucida (Triopa), 66 fe Clinitonia) 1 luniceps (Oscaniopsis), 35 5 (Pleurobranchus), 35 maculata (Pleurobranchaea), 35 Madrella, go Madrella aurantiaca, 90 ij ferruginosa, 90 Marioniae. 82 Marsenia, 104 Marsenia capensis, 105 i leptoconcha, 106 y perspicua, 104 Marseniidae, 104 meckelii (Pleurobranchaea), 33 mediterranea (Idalia), 80 melanopus (Pleurobranchaea), 31 Melibe, 95 Melibe australis, 95 5, bucephala, 96 » Capucina, 96 » fimbriata, 95 » leonina, 96 » ocellata, 95 » papillosa, 96 », pilosa, 96 » Tangli, 95 5» Tosea, 195, 96 vexillifera, 96 microdonta (Pleur aphyllidia), 103 monochroa (Aplysia), 13 morosa (Diaulula), 50 5, (Nembrotha), 68 mucroniferus (Proctonotus), 90, miilleri (Phoronis), 153 natalensis (Pleurophyllidia), 100, 102 Naticidae, 108 Navarchus, 29 Nembrotha, 67 Nembrotha amitina, 68 ” capensis, 68 _ cristata, 68 BA diaphana, 68 edwardsi. 68 5 gracilis, 68 5 gratiosa, 68 i kubaryana, 68 -t lineolata, 68 is morosa, 68 i, nigerrima, 68 Bs rubro-ocellata, 68 ; rubropapulosa, 68 semperi, 68 Nembrothae, 67 niger rima (Nembrotha), 68 nigropunctata (Oscaniella), 37, 38, 39 nodulosa (Reophax), 85 Notarchidae, 19 Notarchus, 19 Notaspidea, 30 Nudibranchiata, 41 Nudibranchiata holohepatica, 82 re kladohepatica, 82 obscurum (Doridium), 29 ocellata (Melibe), 96 ocelligera (Aclesia), 20 ocelligera (Staurodoris), 45 ocelligerum (Doridium), 28 ornata (Kalinga), 75 Oscaniella, 37, 41 Oscaniellae, 37, 38 Oscaniella granulata, 39 *; nigropunctata, 37, 38, 36 Oscaniopsis, 34, 35 Oscaniopsis amboineli, 35 + compta, 35 A luniceps, 35 s pleurobranchaeana. 35 i semperi, 35 Oscanius, 37 “‘pacificus (Euplocamus), 71 pallida (Tritonia), 1, 83, 84 palmiformis (Hyperammina), 18 186 papillosa (Melibe), 96 pecten (Staurodoris), 46 Pectinibranchiata, 104 Pelosina variabilis, 185 perplexa (Doris (Gen. ?)), 53 perspicua (Marsenia), 104 petersi (Pleurophyllidia), toe pilsbryi (Doridium), 28 Philine, 23 Philine aperta, 24, 26 We (Capensiss27 in) .catena,.27, linia, ry LONGED? 3) PFWinosa, 27 » quadrata, 27 » Quadripartita, 2 a sCabray ai » sinuata, 27 velutinoides, 27 philinopsis {Chelidonura), 29 Philinidae, 2: Phorenidea, 151 Phoronis capensis, 151, 152, etc. - hippocrepia, 159 49 buskii, 159 a australis, 158, 169 nt miilleri, 153 Phoronopsis, 152, 153 Phonoropsis albomaculata, 151, 153 pilosa (Melibe), 96 pinnata (Bottelina), 186, 189 Planocera, 145 Planoceridae, 148 planulatus (Sigaretus), 108, 109 planus (Sigaretus), 108 Platydoris arrogans, 61 plebeia (Chelidonura), 29 pleii (Aclesia), 20 Pleurobranchaea, 30 Pleurobranchaea capensis, I, 31, 32 _ melanopus, 31 ‘ meckelii, 33 maculata, 35 pleurobranchaeana (Oscaniopsis), 35 Pleurobranchidae, 30 Pleurobranchus, 37 Pleurobranchus luniceps, 35 * granulatus, I, 39, 40, 41 Pleurophyllidia, 99 PleurophyHidia capensis, 99 + euchroa, 102 7 gilchristi, Tor, 102 35 horatii, roo s microdonta, 103 : natalensis, 100, 102 petersi, 100 Pleurophyllidiidae, 99 poikilia (Aplysia), ro Porostomata, 60: Proctonotus, 90 Proctonotus mucroniferus, 90 propriae (Aplysiidae), 2 pruinosa (Philine), 27 Pseudida (Doris Gen ?). 52 Ptychodera capensis, 151, 172 Pterobranchia, 151 pulchella (Idaliella), 80 punctifera (Thordisa), 57 punctilucens (Doridium), 28 punctulifera (Thordisa), 50, 54 purpureum (Doridium), 28 pusilla, (Aclesia), 20 pustulata (Staurodoris), 46 quadrata (Philine), 27 quadripartita (Philine), 24 rangii (Melibe), 96 reticulatum (Doridium), 29 Reophax, 192 Reophax nodulosa, 185 Rhabdammina discreta 186 Rhabdammininae, 188 Rhizopod, 185 rosea (Melibe), 1, 96 rubro-ocellata (Nembrotha), 68 Frubropapulosa (Nembrotha), 68 Fumphii (Dolabella), 14, 15, 16, 19 sanguineus (Janus), 89 scabra (Philine), 27 schroeteri (Bullia), 2 scripta (Archidoris), 44 semperi (Nembrotha), 68 y (Oscaniopsis), 35 198 | sibogae (Aplysia), 13 Sigaretus planulatus, 108, 16@ A planus, 108 sinuata (Philine), 27 Staurodoris, 45 Staurodoris bertheloti, 45 7 calva, 46 = depressa, 46 ” d’orbignyi. 45 4 januarii, 45, 46 7 pecten, 46 pustulata, 46 verrucosa, 45, 46 striata (Aclesia), 20 Syringammina fragillissima 185 tentaculata (Idalia), 8o teremidi (Dolabella), 15 Tethymelibidae, 94 Thallepus, 19 | Thordisa, 50 | Thordisa punctifera, 50, 51, 57 | tongana (Aplysia), 15 7 (Dolabella), 15 Trevelyanae, 67 tricoloratum (Doridium), Triopa, 65 Triopa catalinae, 66 » €lavigera. 65 » gracilis, 66 » longicornis, 66 », lucida, 66 Tritonia, 83 Tritonia indecora, 85 4) | lucidat a », pallida, 1,83, 84 +i tristis, 66 M yatesi, 66 tristis (Triopa), 66 Tritoniae, 82 Tritonidoxa, 82, 86 Tritonidoxa capensis, 87 Tritoniidae, 82 Tritoniopsis, 82 truncata (Dolabella), 15 variabilis (Pelosina), 185 varians (Chelidonura), 2 | varicolor (Aclesia), 20 | velutina (Chelidonura), 29 velutinoides ¢Philine), 27 verrucosa (Staurodoris), 45, 46 vexillifera (Melibe), 96 woodi (Aplysia), 12 : Zanclopus cephalodisci, 17 yatesi (Tritonia), 66 28 oa god os te*s Naae os aS eae y ee ee Sipe tot a em AY Pomel Ro spar hay? 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