The Henri Bergson Megapack. Henri Bergson
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 singly. That is to say that neo-Lamarckism is no more able than any other form of evolutionism to solve the problem.
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In thus submitting the various present forms of evolutionism to a common test, in showing that they all strike against the same insurmountable difficulty, we have in no wise the intention of rejecting them altogether. On the contrary, each of them, being supported by a considerable number of facts, must be true in its way. Each of them must correspond to a certain aspect of the process of evolution. Perhaps even it is necessary that a theory should restrict itself exclusively to a particular point of view, in order to remain scientific, i.e. to give a precise direction to researches into detail. But the reality of which each of these theories takes a partial view must transcend them all. And this reality is the special object of philosophy, which is not constrained to scientific precision because it contemplates no practical application. Let us therefore indicate in a word or two the positive contribution that each of the three present forms of evolutionism seems to us to make toward the solution of the problem, what each of them leaves out, and on what point this threefold effort should, in our opinion, converge in order to obtain a more comprehensive, although thereby of necessity a less definite, idea of the evolutionary process.
The neo-Darwinians are probably right, we believe, when they teach that the essential causes of variation are the differences inherent in the germ borne by the individual, and not the experiences or behavior of the individual in the course of his career. Where we fail to follow these biologists, is in regarding the differences inherent in the germ as purely accidental and individual. We cannot help believing that these differences are the development of an impulsion which passes from germ to germ across the individuals, that they are therefore not pure accidents, and that they might well appear at the same time, in the same form, in all the representatives of the same species, or at least in a certain number of them. Already, in fact, the theory of mutations is modifying Darwinism profoundly on this point. It asserts that at a given moment, after a long period, the entire species is beset with a tendency to change. The tendency to change, therefore, is not accidental. True, the change itself would be accidental, since the mutation works, according to De Vries, in different directions in the different representatives of the species. But, first we must see if the theory is confirmed by many other vegetable species (De Vries has verified it only by the Œnothera Lamarckiana),[49] and then there is the possibility, as we shall explain further on, that the part played by chance is much greater in the variation of plants than in that of animals, because, in the vegetable world, function does not depend so strictly on form. Be that as it may, the neo-Darwinians are inclined to admit that the periods of mutation are determinate. The direction of the mutation may therefore be so as well, at least in animals, and to the extent we shall have to indicate.
We thus arrive at a hypothesis like Eimer’s, according to which the variations of different characters continue from generation to generation in definite directions. This hypothesis seems plausible to us, within the limits in which Eimer himself retains it. Of course, the evolution of the organic world cannot be predetermined as a whole. We claim, on the contrary, that the spontaneity of life is manifested by a continual creation of new forms succeeding others. But this indetermination cannot be complete; it must leave a certain part to determination. An organ like the eye, for example, must have been formed by just a continual changing in a definite direction. Indeed, we do not see how otherwise to explain the likeness of structure of the eye in species that have not the same history. Where we differ from Eimer is in his claim that combinations of physical and chemical causes are enough to secure the result. We have tried to prove, on the contrary, by the example of the eye, that if there is “orthogenesis” here, a psychological cause intervenes.
Certain neo-Lamarckians do indeed resort to a cause of a psychological nature. There, to our thinking, is one of the most solid positions of neo-Lamarckism. But if this cause is nothing but the conscious effort of the individual, it cannot operate in more than a restricted number of cases—at most in the animal world, and not at all in the vegetable kingdom. Even in animals, it will act only on points which are under the direct or indirect control of the will. And even where it does act, it is not clear how it could compass a change so profound as an increase of complexity: at most this would be conceivable if the acquired characters were regularly transmitted so as to be added together; but this transmission seems to be the exception rather than the rule. A hereditary change in a definite direction, which continues to accumulate and add to itself so as to build up a more and more complex machine, must certainly be related to some sort of effort, but to an effort of far greater depth than the individual effort, far more independent of circumstances, an effort common to most representatives of the same species, inherent in the germs they bear rather than in their substance alone, an effort thereby assured of being passed on to their descendants.
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So we come back, by a somewhat roundabout way, to the idea we started from, that of an original impetus of life, passing from one generation of germs to the following generation of germs through the developed organisms which bridge the interval between the generations. This impetus, sustained right along the lines of evolution among which it gets divided, is the fundamental cause of variations, at least of those that are regularly passed on, that accumulate and create new species. In general, when species have begun to diverge from a common stock, they accentuate their divergence as they progress in their evolution. Yet, in certain definite points, they may evolve identically; in fact, they must do so if the hypothesis of a common impetus be accepted. This is just what we shall have to show now in a more precise way, by the same example we have chosen, the formation of the eye in molluscs and vertebrates. The idea of an “original impetus,” moreover, will thus be made clearer.
Two points are equally striking in an organ like the eye: the complexity of its structure and the simplicity of its function. The eye is composed of distinct parts, such as the sclerotic, the cornea, the retina, the crystalline lens, etc. In each of these parts the detail is infinite. The retina alone comprises three layers of nervous elements—multipolar cells, bipolar cells, visual cells—each of which has its individuality and is undoubtedly a very complicated organism: so complicated, indeed, is the retinal membrane in its intimate structure, that no simple description can give an adequate idea of it. The mechanism of the eye is, in short, composed of an infinity of mechanisms, all of extreme complexity. Yet vision is one simple fact. As soon as the eye opens, the visual act is effected. Just because the act is simple, the slightest negligence on the part of nature in the building of the infinitely complex machine would have made vision impossible. This contrast between the complexity of the organ and the unity of the function is what gives us pause.
A mechanistic theory is one which means to show us the gradual building-up of the machine under the influence of external circumstances intervening either directly by action on the tissues or indirectly by the selection of better-adapted ones. But, whatever form this theory may take, supposing it avails at all to explain