Page:EB1911 - Volume 11.djvu/543

EUTHYNEURA] or disappearance of one phase of shell-formation before a later one is entered upon.

The development of the aquatic Pulmonata from the egg offers considerable facilities for study, and that of Limnaeus has been elucidated by E. R. Lankester, whilst H. Rabl has with remarkable skill applied the method of sections to the study of the minute embryos of Planorbis. The chief features in the development of Limnaeus are exhibited in fig. 60. There is not a very large amount of food-material present in the egg of this snail, and accordingly the cells resulting from division are not so unequal as in many other cases. The four cells first formed are of equal size, and then four smaller cells are formed by division of these four so as to lie at one end of the first four (the pole corresponding to that at which the “directive corpuscles” are extruded and remain). The smaller cells now divide and spread over the four larger cells; at the same time a space—the cleavage cavity or blastocoel—forms in the centre of the mulberry-like mass. Then the large cells recommence the process of division and sink into the hollow of the sphere, leaving an elongated groove, the blastopore, on the surface. The invaginated cells (derived from the division of the four big cells) form the endoderm or arch-enteron; the outer cells are the ectoderm. The blastopore now closes along the middle part of its course, which coincides in position with the future “foot.” One end of the blastopore becomes nearly closed, and an ingrowth of ectoderm takes place around it to form the stomodaeum or fore-gut and mouth. The other extreme end closes, but the invaginated endoderm cells remain in continuity with this extremity of the blastopore, and form the “rectal peduncle” or “pedicle of invagination” of Lankester, although the endoderm cells retain no contact with the middle region of the now closed-up blastopore. The anal opening forms at a late period by a very short ingrowth or proctodaeum coinciding with the blind termination of the rectal peduncle (fig. 60, pi).

The body-cavity and the muscular, fibrous and vascular tissues are traced partly to two symmetrically disposed “mesoblasts,” which bud off from the invaginated arch-enteron, partly to cells derived from the ectoderm, which at a very early stage is connected by long processes with the invaginated endoderm. The external form of the embryo goes through the same changes as in other Gastropods, and is not, as was held previously to Lankester’s observations, exceptional. When the middle and hinder regions of the blastopore are closing in, an equatorial ridge of ciliated cells is formed, converting the embryo into a typical trochosphere.

The foot now protrudes below the mouth, and the post-oral hemisphere of the trochosphere grows more rapidly then the anterior or velar area. The young foot shows a bilobed form. Within the velar area the eyes and the cephalic tentacles commence to rise up, and on the surface of the post-oral region is formed a cap-like shell and an encircling ridge, which gradually increases in prominence and becomes the freely depending mantle-skirt. The outline of the velar area becomes strongly emarginated and can be traced through the more mature embryos to the cephalic lobes or labial processes of the adult Limnaeus (fig. 61).

The increase of the visceral dome, its spiral twisting, and the gradual closure of the space overhung by the mantle-skirt so as to convert it into a lung-sac with a small contractile aperture, belong to stages in the development later than any represented in our figures.

We may now revert briefly to the internal organization at a period when the trochosphere is beginning to show a prominent foot growing out from the area where the mid-region of the elongated blastopore was situated, and having therefore at one end of it the mouth and at the other the anus. Fig. 60 represents such an embryo under slight compression as seen by transmitted light. The ciliated band of the left side of the velar area is indicated by a line extending from v to v; the foot f is seen between the pharynx ph and the pedicle of invagination pi. The mass of the arch-enteron or invaginated endodermal sac has taken on a bilobed form, and its cells are swollen (gs and tge). This bilobed sac becomes entirely the liver in the adult; the intestine and stomach are formed from the pedicle of invagination, whilst the pharynx, oesophagus and crop form from the stomodaeal invagination ph. To the right (in the figure) of the rectal peduncle is seen the deeply invaginated shell-gland ss, with a secretion sh protruding from it. The shell-gland is destined in Limnaeus to become very rapidly stretched out, and to disappear. Farther up, within the velar area, the rudiments of the cerebral nerve-ganglion ng are seen separating from the ectoderm. A remarkable cord of cells having a position just below the integument occurs on each side of the head. In the figure the cord of the left side is seen, marked re. This paired organ consists of a string of cells which are perforated by a duct opening to the exterior and ending internally in a flame-cell. Such cannulated cells are characteristic of the nephridia of many worms, and the organs thus formed in the embryo Limnaeus are embryonic nephridia. The most important fact about them is that they disappear, and are in no way connected with the typical nephridium of the adult. In reference to their first observer they were formerly called “Stiebel’s canals.” Other Pulmonata possess, when embryos, Stiebel’s canals in a more fully developed state, for instance, the common slug Limax. Here too they disappear during embryonic life. Similar larval nephridia occur in other Gastropoda. In the marine Streptoneura they are ectodermic projections which ultimately fall off; in the Opisthobranchs they are closed pouches; in Paludina and Bithynia they are canals as in Pulmonata.

Marine Pulmonata.—Whilst the Pulmonata are essentially a terrestrial and fresh-water group, there is one genus of slug-like Pulmonates which frequent the sea-coast (Oncidium, fig. 62). Karl Semper has shown that these slugs have, in addition to the usual pair of cephalic eyes, a number of eyes developed upon the dorsal integument. These dorsal eyes are very perfect in elaboration, possessing lens, retinal nerve-end cells, retinal pigment and optic nerve. Curiously enough, however, they differ from the cephalic Molluscan eye in the fact that, as in the vertebrate eye, the filaments of the optic nerve penetrate the retina, and are connected with the