of the continuity of the germ-plasm, to regard the germinal cells—ova and spermatozoa—as almost independent of the somatic cells. Starting from this, it has been claimed, and is still claimed by many, that the hereditary transmission of an acquired character is inconceivable. But if, perchance, experiment should show that acquired characters are transmissible, it would prove thereby that the germ-plasm is not so independent of the somatic envelope as has been contended, and the transmissibility of acquired characters would become ipso facto conceivable; which amounts to saying that conceivability and inconceivability have nothing to do with the case, and that experience alone must settle the matter. But it is just here that the difficulty begins. The acquired characters we are speaking of are generally habits or the effects of habit, and at the root of most habits there is a natural disposition. So that one can always ask whether it is really the habit acquired by the soma of the individual that is transmitted, or whether it is not rather a natural aptitude, which existed prior to the habit. This aptitude would have remained inherent in the germ-plasm which the individual bears within him, as it was in the individual himself and consequently in the germ whence he sprang. Thus, for instance, there is no proof that the mole has become blind because it has formed the habit of living underground; it is perhaps because its eyes were becoming atrophied that it condemned itself to a life underground.[40] If this is the case, the tendency to lose the power of vision has been transmitted from germ to germ without anything being acquired or lost by the soma of the mole itself. From the fact that the son of a fencing-master has become a good fencer much more quickly than his father, we cannot infer that the habit of the parent has been transmitted to the child; for certain natural dispositions in course of growth may have passed from the plasma engendering the father to the plasma engendering the son, may have grown on the way by the effect of the primitive impetus, and thus assured to the son a greater suppleness than the father had, without troubling, so to speak, about what the father did. So of many examples drawn from the progressive domestication of animals: it is hard to say whether it is the acquired habit that is transmitted or only a certain natural tendency—that, indeed, which has caused such and such a particular species or certain of its representatives to be specially chosen for domestication. The truth is, when every doubtful case, every fact open to more than one interpretation, has been eliminated, there remains hardly a single unquestionable example of acquired and transmitted peculiarities, beyond the famous experiments of Brown-Séquard, repeated and confirmed by other physiologists.[41] By cutting the spinal cord or the sciatic nerve of guinea-pigs, Brown-Séquard brought about an epileptic state which was transmitted to the descendants. Lesions of the same sciatic nerve, of the restiform body, etc., provoked various troubles in the guinea-pig which its progeny inherited sometimes in a quite different form: exophthalmia, loss of toes, etc. But it is not demonstrated that in these different cases of hereditary transmission there had been a real influence of the soma of the animal on its germ-plasm. Weismann at once objected that the operations of Brown-Séquard might have introduced certain special microbes into the body of the guinea-pig, which had found their means of nutrition in the nervous tissues and transmitted the malady by penetrating into the sexual elements.[42] This objection has been answered by Brown-Séquard himself;[43] but a more plausible one might be raised. Some experiments of Voisin and Peron have shown that fits of epilepsy are followed by the elimination of a toxic body which, when injected into animals,[44] is capable of producing convulsive symptoms. Perhaps the trophic disorders following the nerve lesions made by Brown-Séquard correspond to the formation of precisely this convulsion-causing poison. If so, the toxin passed from the guinea-pig to its spermatozoon or ovum, and caused in the development of the embryo a general disturbance, which, however, had no visible effects except at one point or another of the organism when developed. In that case, what occurred would have been somewhat the same as in the experiments of Charrin, Delamare, and Moussu, where guinea-pigs in gestation, whose liver or kidney was injured, transmitted the lesion to their progeny, simply because the injury to the mother’s organ had given rise to specific “cytotoxins” which acted on the corresponding organ of the foetus.[45] It is true that, in these experiments, as in a former observation of the same physiologists,[46] it was the already formed foetus that was influenced by the toxins. But other researches of Charrin have resulted in showing that the same effect may be produced, by an analogous process, on the spermatozoa and the ova.[47] To conclude, then: the inheritance of an acquired peculiarity in the experiments of Brown-Séquard can be explained by the effect of a toxin on the germ. The lesion, however well localized it seems, is transmitted by the same process as, for instance, the taint of alcoholism. But may it not be the same in the case of every acquired peculiarity that has become hereditary?
There is, indeed, one point on which both those who affirm and those who deny the transmissibility of acquired characters are agreed, namely, that certain influences, such as that of alcohol, can affect at the same time both the living being and the germ-plasm it contains. In such case, there is inheritance of a defect, and the result is as if the soma of the parent had acted on the germ-plasm, although in reality soma and plasma have simply both suffered the action of the same cause. Now, suppose that the soma can influence the germ-plasm, as those believe who hold that acquired characters are transmissible. Is not the most natural hypothesis to suppose that things happen in this second case as in the first, and that the direct effect of the influence of the soma is a general alteration of the germ-plasm? If this is the case, it is by exception, and in some sort by accident, that the modification of the descendant is the same as that of the parent. It is like the hereditability of the alcoholic taint: it passes from father to children, but it may take a different form in each child, and in none of them be like what it was in the father. Let the letter C represent the change in the plasm, C being either positive or negative, that is to say, showing either the gain or loss of certain substances. The effect will not be an exact reproduction of the cause, nor will the change in the germ-plasm, provoked by a certain modification of a certain part of the soma, determine a similar modification of the corresponding part of the new organism in process of formation, unless all the other nascent parts of this organism enjoy a kind of immunity as regards C: the same part will then undergo alteration in the new organism, because it happens that the development of this part is alone subject to the new influence. And, even then, the part might be altered in an entirely different way from that in which the corresponding part was altered in the generating organism.
We should propose, then, to introduce a distinction between the hereditability of deviation and that of character. An individual which acquires a new character thereby deviates from the form it previously had, which form the germs, or oftener the half-germs, it contains would have reproduced in their development. If this modification does not involve the production of substances capable of changing the germ-plasm, or does not so affect nutrition as to deprive the germ-plasm of certain of its elements, it will have no effect on the offspring of the individual. This is probably the case as a rule. If, on the contrary, it has some effect, this is likely to be due to a chemical change which it has induced in the germ-plasm. This chemical change might, by exception, bring about the original modification again in the organism which the germ is about to develop, but there are as many and more chances that it will do something else. In this latter case, the generated organism will perhaps deviate from the normal type as much as the generating organism, but it will do so differently. It will have inherited deviation and not character. In general, therefore, the habits formed by an individual have probably no echo in its offspring; and when they have, the modification in the descendants may have no visible likeness to the original one. Such, at least, is the hypothesis which seems to us most likely. In any case, in default of proof to the contrary, and so long as the decisive experiments called for by an eminent biologist[48] have not been made, we must keep to the actual results of observation. Now, even if we take the most favorable view of the theory of the transmissibility of acquired characters, and assume that the ostensible acquired character is not, in most cases, the more or less tardy development of an innate character, facts show us that hereditary transmission is the exception and not the rule. How, then, shall we expect it to develop an organ such as the eye? When we think of the enormous number of variations, all in the same direction, that we must suppose to be accumulated before the passage from the pigment-spot of the Infusorian to the eye of the mollusc and of the vertebrate is possible, we do not see how heredity, as we observe it, could ever have determined this piling-up of differences, even supposing that individual efforts could have produced each of them
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