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the primitive mouth of the gastrula. The whole mass of the inner and larger and clearer cells (including the white polar region) belongs to the entoderm or ventral layer. The outer envelope of dark smaller cells forms the ectoderm or skin-layer.
In the meantime, a large cavity, full of fluid, has been formed within the globular body--the segmentation-cavity or embryonic cavity (blastocoel, Figures 1.41 to 1.44 F). It extends considerably as the cleavage proceeds, and afterwards assumes an almost semi-circular form (Figure 1.41 F). The frog-embryo now represents a modified embryonic vesicle or blastula, with hollow animal half and solid vegetal half.
Now a second, narrower but longer, cavity arises by a process of folding at the lower pole, and by the falling away from each other of the white entoderm-cells (Figures 1.41 to 1.44 N). This is the primitive gut-cavity or the gastric cavity of the gastrula, progaster or archenteron. It was first observed in the ovum of the amphibia by Rusconi, and so called the Rusconian cavity. The reason of its peculiar narrowness here is that it is, for the most part, full of yelk-cells of the entoderm. These also stop up the whole of the wide opening of the primitive mouth, and form what is known as the "yelk-stopper," which is seen freely at the white round spot at the south pole (P). Around it the ectoderm is much thicker, and forms the border of the primitive mouth, the most important part of the embryo (Figure 1.44 k, k apostrophe). Soon the primitive gut-cavity stretches further and further at the expense of the segmentation-cavity (F), until at last the latter disappears altogether. The two cavities are only separated by a thin partition (Figure 1.43 s). With the formation of the primitive gut our frog-embryo has reached the gastrula stage, though it is clear that this cenogenetic amphibian gastrula is very different from the real palingenetic gastrula we have considered (Figures 1.30 to 1.36).
In the growth of this hooded gastrula we cannot sharply mark