Page:The World's Most Famous Court Trial - 1925.djvu/270

266 The writer has had an exceptional opportunity to determine the exact degrees of resemblance existing between separate offspring derived from a single egg. It so happens that a peculiar species of mammal, the nine-banded armadillo, almost always gives birth to four young at a time. These quadruplets are invariably all the same sex in a litter and are nearly identical in their anatomical details. A study of their embryonic history has proven beyond question that in every case the four embryos are produced by the division of a single normally fertilized egg. Large numbers of advanced sets of quadruplets fetuses were studied statistically with the idea of determining the exact degree or their resemblance. An average or a considerable number of determinations revealed the somewhat startling fact that their coefficient of correlation is .93, which is merely another way of saying that they are 93 per cent identical. The remarkable closeness of this resemblance may be fully appreciated when it is realized that the only structural resemblances belonging to this order of closeness are those existing between the right and left halves of single individuals, and that the next order of resemblance is that between siblings (brothers or sisters) who are only 50 per cent identical.

This, then, is a crucial test of the validity of the assumption that closeness of resemblance is a function of closeness of kinship, for here we have the closest approach to identity in connection with what is also the closest possible blood relationship.

Employing the principle of heredity in a somewhat broader way, and in a way that is hardly likely to be questioned even by the most captious, we account for the common possession of certain structural peculiarities by all members of a given kind or species of animal by saying that characters have been derived from a common ancesterancestor [sic]. It is only a short step in logic to conclude that two closely similar kinds or species of animals have been derived one from the other or from a common species. Once having taken this step we are on the road that leads inevitably to an evolutionary interpretation of natural groups. If the principle of heredity holds for fraternities, for races, for species, where are we to draw the line? It does not seem reasonable to admit that structural resemblances within the fraternity, the race, the species, are accounted for as a product of heredity, and to deny that equally plain resemblances among the species of a genus or among the genera of a family have a hereditary basis. It is logically impossible to draw the line at any level of organic classification, and say that fundamental structural resemblance is the product of heredity up to such and such a level, but that beyond some arbitrarily settled point heredity ceases to operate.

The foundation stones of comparative anatomy are the principles of homology and of analogy. The former implies heredity and the latter variation.

Any one who has at all seriously studied comparative anatomy must have been impressed with the fact that the animal kingdom exhibits several distinct types of architecture, each of which characterizes one of the grand divisions of the kingdom. Within each of these great assemblages of animals characterized by a common plan of organization there are almost innumerable structural diversities within the scope of the fundamental plan. These major or minor departures from the ideally generalized condition reminded one of variations upon a theme in music; no matter how elaborate the variations may be, the skilled musician recognizes the common theme running through it all. This fundamental unity amidst minor diversity of form or of function is looked upon as a common inheritance from a more or less remote ancestor. In animals belonging to the same group, and therefore having the