Thus, the only reasonable interpretation is the inheritance of acquired characters. If the effects of use and disuse, which are known causes of change in each individual, influence succeeding individuals—if functionally-produced modifications of structure are transmissible, as well as modifications of structure otherwise arising—then this reduction of the whale's hind limbs to minute rudiments is accounted for. The cause has been unceasingly operative on all individuals of the species ever since the transformation began.

In one case see all. If this cause has thus operated on the limbs of the whale, it has thus operated in all creatures on all parts having active functions.

* * * * *

At the outset I intimated that I must limit my replies to those arguments of Professor Weismann which are contained in his first article. That those contained in his second might be dealt with no less effectually, did time and space permit, is manifest to me; but about the probability of this the reader must form his own judgment. My replies thus far may be summed up as follows:—

Professor Weismann says he has disproved the conclusion that degeneration of the little toe has resulted from inheritance of acquired characters. But his reasoning fails against an interpretation he overlooks. A profound modification of the hind limbs and their appendages must have taken place during the transition from arboreal habits to terrestrial habits; and dwindling of the little toe is an obvious consequence of disuse, at the same time that enlargement of the great toe is an obvious consequence of increased use.

The entire argument based on the unlike forms and instincts presented by castes of social insects is invalidated by an omission. Until probable conclusions are reached respecting the characters which such insects brought with them into the organized social state, no valid inferences can be drawn respecting characters developed during that state.

A further large error of interpretation is involved in the assumption that the different caste-characters are transmitted to them in the eggs laid by the mother insect. While we have evidence that the unlike structures of the sexes are determined by nutrition of the germ before egg-laying, we have evidence that the unlike structures of classes are caused by unlikenesses of nutrition of the larvæ. That these varieties of forms do not result from varieties of germ-plasms, is demonstrated by the fact that where there are varieties of germ-plasms, as in varieties of the same species of mammal, no deviations in feeding prevent display of their structural results.

For such caste-modifications as those of the Amazon-ants, which are unable to feed themselves, there is a feasible explanation other than Professor Weismann's. The relation of common ants to their domestic animals—aphides and coccids—which yield them food on solicitation, does not differ widely from this relation between these Amazon-ants and their domestic animals—the slave-ants. And the habit of being fed, contracted during the first stages of their parasitic life, when there were perfect males and females, may, during that stage, have become established by inheritance. Meanwhile the opposed interpretation—that this incapacity has resulted from the selection of those ant-communities the queens of which laid eggs that had so varied as to entail this incapacity—implies that a scarcely appreciable economy of nerve-matter advantaged the stirp so greatly as to cause it to spread more than other stirps: an incredible supposition.

As the outcome of these alternative interpretations we saw that the argument respecting the co-adaptation of co-operative parts, which Professor Weismann thinks is furnished to him by the Amazon-ants, disappears. The ancestral ants were conquering ants. These founded the communities; and hence those members of the present communities which are most like them are the Amazon-ants. If so, the co-adaptation of the co-operative parts was effected by inheritance during the solitary and semi-social stages. Even were there no such solution, the opposed solution will be unacceptable. These simultaneous appropriate variations of the co-operative parts in sizes, shapes, and proportions, are supposed to be effected by simultaneous variations in the "determinants" of the germ-plasms; and in the absence of an assigned physical cause, this implies a fortuitous concourse of appropriate variations, which carries us back to a "fortuitous concourse of atoms." This may just as well be extended to the entire organism. The old hypothesis of special creations is more consistent and comprehensible.

To rebut my inference drawn from the distribution of discriminativeness, Professor Weismann uses not an argument but the blank form of an argument. The ability to discriminate one twenty-fourth of an inch by the tongue-tip may have been useful to the ape: no conceivable use being even suggested. And then the great body of my argument derived from the distribution of discriminativeness over the skin, which amply suffices, is wholly ignored.