Anatomy, Comparative; Embryology, Human; Evolution; Human beings -- Origin
white region at the south pole corresponds, as we shall see
afterwards, to 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 off the
various stages which we distinguish successively in the bell-gastrula
as morula and gastrula. Nevertheless, it is not difficult to reduce
the whole cenogenetic or disturbed development of this amphigastrula
to the true palingenetic formation of the archigastrula of the
amphioxus.
(FIGURE 1.45. Blastula of the water-salamander (Triton). fh
segmentation-cavity, dz yelk-cells, rz border-zone. (From Hertwig.)
FIGURE 1.46. Embryonic vesicle of triton (blastula), outer view, with
the transverse fold of the primitive mouth (u). (From Hertwig.)
FIGURE 1.47. Sagittal section of a hooded-embryo (depula) of triton
(blastula at the commencement of gastrulation). ak outer germinal
layer, ik inner germinal layer, fh segmentation-cavity, ud primitive
gut, u primitive mouth, dl and vl dorsal and ventral lips of the
mouth, dz yelk-cells. (From Hertwig.))
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