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Volume 78, 1950
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II. Life History i. Struthiolaria papulosa

As in most incubating molluses, reproduction probably takes place all the year round, ovigerous females being collected at Auckland during November, December, April, June, August, and September. As many as 1,000 to 1,500 capsules are contained in the pouch, and a total of 20,000–30,000 veligers are thus liberated from a single brood. An early stage in development removed from the pouch (Pl. 55, Fig. 2) represents an abbreviated two-lobed veliger, approximately 0·5 mm. in length, with a pair of short, undivided velar rudiments projecting laterally. The visceral mass is opaque and yolky, covered by a shell rudiment, in the form of a delicate chitinous cap, while the head region forms a large spherical protuberance with neither eyes nor otocysts visible. The foot is present as a short, tongue-shaped lobe, behind the head, and the embryos move about freely within the capsule, mainly by muscular movements of the velar lobes.

At the final stage in incubation, when the capsules have attained approximately twice their original size, and the large four-lobed veligers can be clearly identified within, the pallial margin is widely extended over the lip of the shell, bringing the pouch aperture to an external position, and a string of capsules is extruded, the veligers at once breaking through the capsule membrane and commencing to swim freely. The expanded velum (Pl. 55. Fig. 1 VL.) now measures 1 ½ 2 mm. across, deeply subdivided to form a pair of large swimming lobes at either side. Near the tip of each lobe is a very conspicuous yellowish-brown spot, from which a yellow band extends around the velum just inside the margin. The thickened rim of the velum is beset, with stiff, robust, cilia, approximately 15μ in length, which serve, together with movements of the velar lobes themselves, for the rapid propulsion of the larva. The larval shell (sh) is at this stage 0·3 mm. in height and a little less in width, chitinous, perfectly transparent, without sculpture and forming a tiny wide-mouthed cup. with a short, single-whorled planorboid coil. The foot (ft) lying behind the velum is narrow and squarish along the anterior edge, becoming wider and oval behind, the whole surface glandular and finely ciliated. No opercular rudiment is yet present. The cephalic tentacles are short and clubshaped, tipped with several longish sensory cilia. The eyes are prominent at the tentacle bases, and the otocysts distinctly seen within the head cavity. The etnidial filaments are not yet elongated as in the adult, and ciliary feeding apparently does not occur at this stage.

The alimentary canal (Pl. 55, Fig. 3) shows essentially its adult form. The buccal bulb with its minute radular rudiment leads into the narrow, strongly ciliated oesophagus, passing back to the stomach—a transparent globular sac, provided with a short caecum from which projects a perfectly developed crystalline style, rotating clockwise 40 times a minute, with a mucus-bound mass of food material attached to the gastric end. The two digestive gland lobes are filled with brownish yolky contents, and there is a two-way pasage of particles along the diverticula leading out of the stomach. The intestine is a narrow ciliated tube encircling the renal organ, and continuing to

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the mantle edge as a short, wide rectum. The kidney (Pl. 55, Fig. 3 kd), which as in all marine prosobranchiates gives rise directly to the adult renal organ, is a large flattened or spherical sac on the right pallial wall, extending forward almost to the mantle margin. Its large hexagonal lining cells each contain a dark granular spherule somewhat resembling a nucleus, and the sac undergoes regular pulsatile movements. The two-chambered definitive heart (ht) lies in the pericardium and there is as well a pulsatile larval heart or thoracic vesicle (lh) formed by a dilation of the anterior aorta beneath the pallial cavity floor, which projects in diastole from the aperture of the pallial cavity.

The later development of Struthiolaria papulosa has not been worked out. From the evidence of the 2 ½-whorled protoconch, and the extremely well-developed swimming organs, it seems clear that there is a fairly long stage of planktonic existence. Tow net samples taken at Cheltenham (2.49) yielded one veliger that from size, shell sculpture, and general appearance could be tentatively recognised as a Strutiolaria at the 2-whorled stage, towards the end of larval life. The velum was damaged and withdrawn, although, from the striking resemblance of the four-lobed larva to that of the related Aporrhais, it may well be that, as in the latter genus, the final stage larva of Struthiolaria possesses a six-lobed velum.

ii. Pelicaria vermis

In the genus Pelicaria the embryos are completely incubated in the pouch, and are liberated as tiny replicas of the adult which at once take on a benthic existence. The female reproductive apparatus is in general closely similar to that of Struthiolaria. The albumen gland is, however, shorter, and relatively stouter, the receptaculum forms a smaller bulbous sac, while the capsule gland is relatively more spacious, a single elongate egg capsule occupying its whole length. Only seven or eight capsules are contained in the pouch at one time, each 7 mm. long, elongate-ovoid, not joined in a string, and each containing five eggs, approximately 1·0 mm. across and white in colour (Text Fig. 3). Liberation of the embryos normally takes place when the shell is 4 ½–5 mm. in length, with two rounded whorls and the typical apex of this genus. A thin-walled, elongate, capuliform bulb (Pl. 55, Fig. 4) is placed transversely to the long axis of the shell, being at first transparent and entirely chitinous. It is followed by a calcified spirally coiled region sculptured with fine spiral cinguli from the beginning of the second whorl. As may be seen, this apex differs markedly from the small planorboid tip in Struthiolaria. On liberation, the embryo (Fig. 6), which is translucent milk-white in colour, at once begins in crawl about and to execute the characteristic movements of the adult. The sole is long and narrow, with an opercular spine present by which the typical “righting” movement of the adult can already be performed.

Plate 55, Fig. 5, represents an embryo removed from the pouch at an earlier stage of development. The shell measures 1 ½–2 mm. in length, consisting of a capuliform apex and a single finely spirally sculptured whorl. These embryos move about actively within the capsule, by the action of the foot, and finally break through the enclosing membrane by the use of the opercular spine. A large vestige

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Fig. 1—Struthiolaria papulosa. Four-lobed veliger larva after liberation from the incubatory pouch, X 30.
Fig. 2—Struthiolaria papulosa. Earlier (two-lobed) veliger removed from the incubatory pouch, X 35.
Fig. 3—Struthiolaria papulosa. Enlarged sketch of veliger at stage shown in Fig. 1, illustrating structural details.
Fig. 4—Pelicaria vermis. Apex of adult shell, intact (above) and broken, with calcareous septum developed (below).
Fig. 5—Pelicaria vermis. Embryo with rudimentary velum, during incubation in the pouch, X 30.
Fig. 6—Pelicaria vermis. Embryo after liberation from the pouch, at the beginning of the benthic stage, X 8.
AP. apex; CE, cerebral ganglion; CT, ctenidium; DIG, digestive gland; F, foot; HT, definitive heart; KD, kidney; LH, larval heart or “thoracic vesicle”; M, mouth; NR. nerve ring; OP, operculum; OT. otocyst; PA. pallial margin; PR, proboscis; PT, pallial tentacles; SH, shell; SM. stomach; ST, style caecum; V, velum; VL, velar lobe.

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of the velum is retained in the form of a transverse rectangular flap (vf) surrounding the head region in front of the foot, with a rim of marginal cilia keeping up an active beat. There is no coloration as on the velar lobes of Struthiolaria, and the organ is lost completely before the embryo normally emerges. The gill has developed the same proportions as in the ciliary feeding adult, and a long fringe of free, rod-like filaments generally projects obliquely forward over the margin of the mantle. The renal organ resembles that of the adult, but the larval heart is still prominent. The foot is oval behind, with an opercular spine developed and two broad tracts of gland cells along the sole. Its anterior end is squarish and strongly ciliated, incised along the edge by a deep transverse groove.

In laboratory tanks are embryos frequently liberated at this early stage of development, enclosed in the capsules, which fact may indicate a fairly recent acquisition of the incubating habit. It was not discovered how well equipped these velate embryos may be for free existence, though they begin to feed as soon as they emerge from the capsule. Certain ciliary currents appear to be adapted for food collecting. There is a strong rotatory current along the food groove, though detrital contents were not seen. Immediately on liberation, however, a strong ciliary current was observed to carry a string of fine plant debris along the groove of the anterior edge of the foot, which was always held turned upwards close to the mouth. Periodically the string was ingested, and it seems that at the earliest free-living stage the ciliated groove of the foot may replace the food groove in collecting nutriment.

Comparative

The female genital ducts of the related Aporrhais pes-pelicani were dissected for comparison with Struthiolaria, and were found to agree closely in general plan, though there are a number of differences in detail. The albumen gland (Text Fig. 4 alb) is a smooth-walled, curved tube receiving anteriorly the duct of a spacious cylindrical receptaculum (rec) lying for the most part below the albumen gland. The capsule gland (cps) is very short, remaining ventrally unclosed, and leading into a ciliated genital groove, which runs forward as in the strombids as far as the anterior edge of the foot. There is no incubatory pouch, and Lebour (1933) has recorded the deposition of eggs 0·24 mm. across, laid singly attached to sand grains or debris. The first free-swimming stage is a two-lobed veliger, metamorphosing to a four-lobed larva closely resembling in detail the corresponding stage in Struthiolaria, even to the brown spot at the end of each velar lobe.

Aporrhais, Struthiolaria, and Pelicaria thus show an evolutionary series in reproductive habits: in Aporrhais single eggs are deposited separately and the larval history is unabbreviated; in Struthiolaria a large number of fairly small eggs is enclosed in a common capsule, and partial incubation takes place, with the retention of the young to the four-lobed veliger stage; in Pelicaria the eggs are reduced in number and large and yolky, the free-swimming stage being wholly eliminated and the embryos liberated at the benthic stage.

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The Struthiolariid Apex

The significance of the apex difference in Struthiolaria and Pelicaria, discussed by Finlay (1931), becomes fairly clear with the elucidation of the life history. Struthiolaria possesses a small, close-coiled, multispiral, calcareous protoconch as typified by S. papulosa. In Pelicaria the tip of the shell forms originally a horny, capuliform bulb, as seen in the fragile apex of the pouch embryo. In the course of development, this chitinous coating is gradually filled up with a structureless calcareous deposit as the animal recedes from the extreme tip, until in the adult a solid blob is formed, sometimes narrowly perforated. The horny coating is soon rubbed off during development, while in a large number of cases the fragile bulb may be detached or damaged at an early stage, and the tip of the shell is then plugged by a similar blob of shelly material deposited within the broken edge, a short distance down from the original apex. As Finlay has surmised, the Pelicaria apex of the scaphelloid type is clearly derived from the multispiral, calcareous type of Struthiolaria. The difference is probably due simply to the increase in the size of the egg in species in which the embryo is incubated. In those forms where there is a long free-swimming stage, the egg is relatively small, and the shell apex is first formed as a tiny cap covering the visceral mass of the embryo formed from the yolky hemisphere of the egg. Where incubation occurs the embryo must live for some time on its yolk reserves, and the egg is much more bulky, with the visceral cap correspondingly large, and of capuliform shape. Though, as Finlay lays down, the multispiral and paucispiral forms will generally be found to be entitled to separate generic status, the distinction may not always be of fundamental importance as a taxonomic character. Thus, for example, in the case of Littorina saxatilis. Seshappa (1947) has drawn attention to the existence of oviparous and ovoviviparous races, apparently characterised by apex differences, within a group classically regarded as forming a single species.