Anatomy, Comparative; Embryology, Human; Evolution; Human beings -- Origin
embryo momentarily assumes.
To give a few examples, we can infer from the fact that the human ovum
is a simple cell that the first ancestor of our species was a tiny
unicellular being, something like the amœba. In the same way, we know,
from the fact that the human fœtus consists, at the first, of two
simple cell-layers (the _ gastrula_), that the _gastræa_, a form with
two such layers, was certainly in the line of our ancestry. A later
human embryonic form (the _chordula_) points just as clearly to a
worm-like ancestor (the _prochordonia_), the nearest living relation of
which is found among the actual ascidiæ. To this succeeds a most
important embryonic stage (_acrania_), in which our headless fœtus
presents, in the main, the structure of the lancelet. But we can only
indirectly and approximately, with the aid of comparative anatomy and
ontogeny, conjecture what lower forms enter into the chain of our
ancestry between the gastræa and the chordula, and between this and the
lancelet. In the course of the historical development many intermediate
structures have gradually fallen out, which must certainly have been
represented in our ancestry. But, in spite of these many, and sometimes
very appreciable, gaps, there is no contradiction between the two
successions. In fact, it is the chief purpose of this work to prove the
real harmony and the original parallelism of the two. I hope to show,
on a substantial basis of facts, that we can draw most important
conclusions as to our genealogical tree from the actual and
easily-demonstrable series of embryonic changes. We shall then be in a
position to form a general idea of the wealth of animal forms which
have figured in the direct line of our ancestry in the lengthy history
of organic life.
In this evolutionary appreciation of the facts of embryology we must,
of course, take particular care to distinguish sharply and clearly
between the primitive, palingenetic (or ancestral) evolutionary
processes and those due to cenogenesis.[2] By _palingenetic_ processes,
or embryonic _recapitulations,_ we understand all those phenomena in
the development of the individual which are transmitted from one
generation to another by heredity, and which, on that account, allow us
to draw direct inferences as to corresponding structures in the
development of the species. On the other hand, we give the name of
_cenogenetic_ processes, or embryonic _variations,_ to all those
phenomena in the fœtal development that cannot be traced to inheritance
from earlier species, but are due to the adaptation of the fœtus, or
the infant-form, to certain conditions of its embryonic development.
These cenogenetic phenomena are foreign or later additions; they allow
us to draw no direct inference whatever as to corresponding processes
in our ancestral history, but rather hinder us from doing so.
Public-domain text, read in full here on John Shaqi.
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