Creative Evolution Part 2

Such is the philosophy of life to which we are leading up. It claims to transcend both mechanism and finalism; but, as we announced at the beginning, it is nearer the second doctrine than the first. It will not be amiss to dwell on this point, and show more precisely how far this philosophy of life resembles finalism and wherein it is different.

Like radical finalism, although in a vaguer form, our philosophy represents the organized world as a harmonious whole. But this harmony is far from being as perfect as it has been claimed to be. It admits of much discord, because each species, each individual even, retains only a certain impetus from the universal vital impulsion and tends to use this energy in its own interest. In this consists _adaptation_. The species and the individual thus think only of themselves--whence arises a possible conflict with other forms of life. Harmony, therefore, does not exist in fact; it exists rather in principle; I mean that the original impetus is a _common_ impetus, and the higher we ascend the stream of life the more do diverse tendencies appear complementary to each other. Thus the wind at a street-corner divides into diverging currents which are all one and the same gust. Harmony, or rather "complementarity," is revealed only in the ma.s.s, in tendencies rather than in states. Especially (and this is the point on which finalism has been most seriously mistaken) harmony is rather behind us than before.

It is due to an ident.i.ty of impulsion and not to a common aspiration. It would be futile to try to a.s.sign to life an end, in the human sense of the word. To speak of an end is to think of a pre-existing model which has only to be realized. It is to suppose, therefore, that all is given, and that the future can be read in the present. It is to believe that life, in its movement and in its entirety, goes to work like our intellect, which is only a motionless and fragmentary view of life, and which naturally takes its stand outside of time. Life, on the contrary, progresses and _endures_ in time. Of course, when once the road has been traveled, we can glance over it, mark its direction, note this in psychological terms and speak as if there had been pursuit of an end.

Thus shall we speak ourselves. But, of the road which was going to be traveled, the human mind could have nothing to say, for the road has been created _pari pa.s.su_ with the act of traveling over it, being nothing but the direction of this act itself. At every instant, then, evolution must admit of a psychological interpretation which is, from our point of view, the best interpretation; but this explanation has neither value nor even significance except retrospectively. Never could the finalistic interpretation, such as we shall propose it, be taken for an antic.i.p.ation of the future. It is a particular mode of viewing the past in the light of the present. In short, the cla.s.sic conception of finality postulates at once too much and too little: it is both too wide and too narrow. In explaining life by intellect, it limits too much the meaning of life: intellect, such at least as we find it in ourselves, has been fas.h.i.+oned by evolution during the course of progress; it is cut out of something larger, or, rather, it is only the projection, necessarily on a plane, of a reality that possesses both relief and depth. It is this more comprehensive reality that true finalism ought to reconstruct, or, rather, if possible, embrace in one view. But, on the other hand, just because it goes beyond intellect--the faculty of connecting the same with the same, of perceiving and also of producing repet.i.tions--this reality is undoubtedly creative, _i.e._ productive of effects in which it expands and transcends its own being. These effects were therefore not given in it in advance, and so it could not take them for ends, although, when once produced, they admit of a rational interpretation, like that of the manufactured article that has reproduced a model. In short, the theory of final causes does not go far enough when it confines itself to ascribing some intelligence to nature, and it goes too far when it supposes a pre-existence of the future in the present in the form of idea. And the second theory, which sins by excess, is the outcome of the first, which sins by defect. In place of intellect proper must be subst.i.tuted the more comprehensive reality of which intellect is only the contraction. The future then appears as expanding the present: it was not, therefore, contained in the present in the form of a represented end. And yet, once realized, it will explain the present as much as the present explains it, and even more; it must be viewed as an end as much as, and more than, a result. Our intellect has a right to consider the future abstractly from its habitual point of view, being itself an abstract view of the cause of its own being.

It is true that the cause may then seem beyond our grasp. Already the finalist theory of life eludes all precise verification. What if we go beyond it in one of its directions? Here, in fact, after a necessary digression, we are back at the question which we regard as essential: can the insufficiency of mechanism be proved by facts? We said that if this demonstration is possible, it is on condition of frankly accepting the evolutionist hypothesis. We must now show that if mechanism is insufficient to account for evolution, the way of proving this insufficiency is not to stop at the cla.s.sic conception of finality, still less to contract or attenuate it, but, on the contrary, to go further.

Let us indicate at once the principle of our demonstration. We said of life that, from its origin, it is the continuation of one and the same impetus, divided into divergent lines of evolution. Something has grown, something has developed by a series of additions which have been so many creations. This very development has brought about a dissociation of tendencies which were unable to grow beyond a certain point without becoming mutually incompatible. Strictly speaking, there is nothing to prevent our imagining that the evolution of life might have taken place in one single individual by means of a series of transformations spread over thousands of ages. Or, instead of a single individual, any number might be supposed, succeeding each other in a unilinear series. In both cases evolution would have had, so to speak, one dimension only. But evolution has actually taken place through millions of individuals, on divergent lines, each ending at a crossing from which new paths radiate, and so on indefinitely. If our hypothesis is justified, if the essential causes working along these diverse roads are of psychological nature, they must keep something in common in spite of the divergence of their effects, as school-fellows long separated keep the same memories of boyhood. Roads may fork or by-ways be opened along which dissociated elements may evolve in an independent manner, but nevertheless it is in virtue of the primitive impetus of the whole that the movement of the parts continues. Something of the whole, therefore, must abide in the parts; and this common element will be evident to us in some way, perhaps by the presence of identical organs in very different organisms.

Suppose, for an instant, that the mechanistic explanation is the true one: evolution must then have occurred through a series of accidents added to one another, each new accident being preserved by selection if it is advantageous to that sum of former advantageous accidents which the present form of the living being represents. What likelihood is there that, by two entirely different series of accidents being added together, two entirely different evolutions will arrive at similar results? The more two lines of evolution diverge, the less probability is there that accidental outer influences or accidental inner variations bring about the construction of the same apparatus upon them, especially if there was no trace of this apparatus at the moment of divergence. But such similarity of the two products would be natural, on the contrary, on a hypothesis like ours: even in the latest channel there would be something of the impulsion received at the source. _Pure mechanism, then, would be refutable, and finality, in the special sense in which we understand it, would be demonstrable in a certain aspect, if it could be proved that life may manufacture the like apparatus, by unlike means, on divergent lines of evolution; and the strength of the proof would be proportional both to the divergency between the lines of evolution thus chosen and to the complexity of the similar structures found in them._

It will be said that resemblance of structure is due to sameness of the general conditions in which life has evolved, and that these permanent outer conditions may have imposed the same direction on the forces constructing this or that apparatus, in spite of the diversity of transient outer influences and accidental inner changes. We are not, of course, blind to the role which the concept of _adaptation_ plays in the science of to-day. Biologists certainly do not all make the same use of it. Some think the outer conditions capable of causing change in organisms in a _direct_ manner, in a definite direction, through physico-chemical alterations induced by them in the living substance; such is the hypothesis of Eimer, for example. Others, more faithful to the spirit of Darwinism, believe the influence of conditions works _indirectly_ only, through favoring, in the struggle for life, those representatives of a species which the chance of birth has best adapted to the environment. In other words, some attribute a _positive_ influence to outer conditions, and say that they actually _give rise to_ variations, while the others say these conditions have only a _negative_ influence and merely _eliminate_ variations. But, in both cases, the outer conditions are supposed to bring about a precise adjustment of the organism to its circ.u.mstances. Both parties, then, will attempt to explain mechanically, by adaptation to similar conditions, the similarities of structure which we think are the strongest argument against mechanism. So we must at once indicate in a general way, before pa.s.sing to the detail, why explanations from "adaptation" seem to us insufficient.

Let us first remark that, of the two hypotheses just described, the latter is the only one which is not equivocal. The Darwinian idea of adaptation by automatic elimination of the unadapted is a simple and clear idea. But, just because it attributes to the outer cause which controls evolution a merely negative influence, it has great difficulty in accounting for the progressive and, so to say, rectilinear development of complex apparatus such as we are about to examine. How much greater will this difficulty be in the case of the similar structure of two extremely complex organs on two entirely different lines of evolution! An accidental variation, however minute, implies the working of a great number of small physical and chemical causes. An acc.u.mulation of accidental variations, such as would be necessary to produce a complex structure, requires therefore the concurrence of an almost infinite number of infinitesimal causes. Why should these causes, entirely accidental, recur the same, and in the same order, at different points of s.p.a.ce and time? No one will hold that this is the case, and the Darwinian himself will probably merely maintain that identical effects may arise from different causes, that more than one road leads to the same spot. But let us not be fooled by a metaphor. The place reached does not give the form of the road that leads there; while an organic structure is just the acc.u.mulation of those small differences which evolution has had to go through in order to achieve it. The struggle for life and natural selection can be of no use to us in solving this part of the problem, for we are not concerned here with what has perished, we have to do only with what has survived. Now, we see that identical structures have been formed on independent lines of evolution by a gradual acc.u.mulation of effects. How can accidental causes, occurring in an accidental order, be supposed to have repeatedly come to the same result, the causes being infinitely numerous and the effect infinitely complicated?

The principle of mechanism is that "the same causes produce the same effects." This principle, of course, does not always imply that the same effects must have the same causes; but it does involve this consequence in the particular case in which the causes remain visible in the effect that they produce and are indeed its const.i.tutive elements. That two walkers starting from different points and wandering at random should finally meet, is no great wonder. But that, throughout their walk, they should describe two identical curves exactly superposable on each other, is altogether unlikely. The improbability will be the greater, the more complicated the routes; and it will become impossibility, if the zigzags are infinitely complicated. Now, what is this complexity of zigzags as compared with that of an organ in which thousands of different cells, each being itself a kind of organism, are arranged in a definite order?

Let us turn, then, to the other hypothesis, and see how it would solve the problem. Adaptation, it says, is not merely elimination of the unadapted; it is due to the positive influence of outer conditions that have molded the organism on their own form. This time, similarity of effects will be explained by similarity of cause. We shall remain, apparently, in pure mechanism. But if we look closely, we shall see that the explanation is merely verbal, that we are again the dupes of words, and that the trick of the solution consists in taking the term "adaptation" in two entirely different senses at the same time.

If I pour into the same gla.s.s, by turns, water and wine, the two liquids will take the same form, and the sameness in form will be due to the sameness in adaptation of content to container. Adaptation, here, really means mechanical adjustment. The reason is that the form to which the matter has adapted itself was there, ready-made, and has forced its own shape on the matter. But, in the adaptation of an organism to the circ.u.mstances it has to live in, where is the pre-existing form awaiting its matter? The circ.u.mstances are not a mold into which life is inserted and whose form life adopts: this is indeed to be fooled by a metaphor.

There is no form yet, and the life must create a form for itself, suited to the circ.u.mstances which are made for it. It will have to make the best of these circ.u.mstances, neutralize their inconveniences and utilize their advantages--in short, respond to outer actions by building up a machine which has no resemblance to them. Such adapting is not _repeating_, but _replying_,--an entirely different thing. If there is still adaptation, it will be in the sense in which one may say of the solution of a problem of geometry, for example, that it is adapted to the conditions. I grant indeed that adaptation so understood explains why different evolutionary processes result in similar forms: the same problem, of course, calls for the same solution. But it is necessary then to introduce, as for the solution of a problem of geometry, an intelligent activity, or at least a cause which behaves in the same way.

This is to bring in finality again, and a finality this time more than ever charged with anthropomorphic elements. In a word, if the adaptation is pa.s.sive, if it is mere repet.i.tion in the relief of what the conditions give in the mold, it will build up nothing that one tries to make it build; and if it is active, capable of responding by a calculated solution to the problem which is set out in the conditions, that is going further than we do--too far, indeed, in our opinion--in the direction we indicated in the beginning. But the truth is that there is a surrept.i.tious pa.s.sing from one of these two meanings to the other, a flight for refuge to the first whenever one is about to be caught _in flagrante delicto_ of finalism by employing the second. It is really the second which serves the usual practice of science, but it is the first that generally provides its philosophy. In any _particular_ case one talks as if the process of adaptation were an effort of the organism to build up a machine capable of turning external circ.u.mstances to the best possible account: then one speaks of adaptation _in general_ as if it were the very impress of circ.u.mstances, pa.s.sively received by an indifferent matter.

But let us come to the examples. It would be interesting first to inst.i.tute here a general comparison between plants and animals. One cannot fail to be struck with the parallel progress which has been accomplished, on both sides, in the direction of s.e.xuality. Not only is fecundation itself the same in higher plants and in animals, since it consists, in both, in the union of two nuclei that differ in their properties and structure before their union and immediately after become equivalent to each other; but the preparation of s.e.xual elements goes on in both under like conditions: it consists essentially in the reduction of the number of chromosomes and the rejection of a certain quant.i.ty of chromatic substance.[22] Yet vegetables and animals have evolved on independent lines, favored by unlike circ.u.mstances, opposed by unlike obstacles. Here are two great series which have gone on diverging. On either line, thousands and thousands of causes have combined to determine the morphological and functional evolution. Yet these infinitely complicated causes have been consummated, in each series, in the same effect. And this effect, could hardly be called a phenomenon of "adaptation": where is the adaptation, where is the pressure of external circ.u.mstances? There is no striking utility in s.e.xual generation; it has been interpreted in the most diverse ways; and some very acute enquirers even regard the s.e.xuality of the plant, at least, as a luxury which nature might have dispensed with.[23] But we do not wish to dwell on facts so disputed. The ambiguity of the term "adaptation," and the necessity of transcending both the point of view of mechanical causality and that of anthropomorphic finality, will stand out more clearly with simpler examples. At all times the doctrine of finality has laid much stress on the marvellous structure of the sense-organs, in order to liken the work of nature to that of an intelligent workman. Now, since these organs are found, in a rudimentary state, in the lower animals, and since nature offers us many intermediaries between the pigment-spot of the simplest organisms and the infinitely complex eye of the vertebrates, it may just as well be alleged that the result has been brought about by natural selection perfecting the organ automatically.

In short, if there is a case in which it seems justifiable to invoke adaptation, it is this particular one. For there may be discussion about the function and meaning of such a thing as s.e.xual generation, in so far as it is related to the conditions in which it occurs; but the relation of the eye to light is obvious, and when we call this relation an adaptation, we must know what we mean. If, then, we can show, in this privileged case, the insufficiency of the principles invoked on both sides, our demonstration will at once have reached a high degree of generality.

Let us consider the example on which the advocates of finality have always insisted: the structure of such an organ as the human eye. They have had no difficulty in showing that in this extremely complicated apparatus all the elements are marvelously co-ordinated. In order that vision shall operate, says the author of a well-known book on _Final Causes_, "the sclerotic membrane must become transparent in one point of its surface, so as to enable luminous rays to pierce it;... the cornea must correspond exactly with the opening of the socket;... behind this transparent opening there must be refracting media;... there must be a retina[24] at the extremity of the dark chamber;... perpendicular to the retina there must be an innumerable quant.i.ty of transparent cones permitting only the light directed in the line of their axes to reach the nervous membrane,"[25] etc. etc. In reply, the advocate of final causes has been invited to a.s.sume the evolutionist hypothesis.

Everything is marvelous, indeed, if one consider an eye like ours, in which thousands of elements are coordinated in a single function. But take the function at its origin, in the Infusorian, where it is reduced to the mere impressionability (almost purely chemical) of a pigment-spot to light: this function, possibly only an accidental fact in the beginning, may have brought about a slight complication of the organ, which again induced an improvement of the function. It may have done this either directly, through some unknown mechanism, or indirectly, merely through the effect of the advantages it brought to the living being and the hold it thus offered to natural selection. Thus the progressive formation of an eye as well contrived as ours would be explained by an almost infinite number of actions and reactions between the function and the organ, without the intervention of other than mechanical causes.

The question is hard to decide, indeed, when put directly between the function and the organ, as is done in the doctrine of finality, as also mechanism itself does. For organ and function are terms of different nature, and each conditions the other so closely that it is impossible to say _a priori_ whether in expressing their relation we should begin with the first, as does mechanism, or with the second, as finalism requires. But the discussion would take an entirely different turn, we think, if we began by comparing together two terms of the same nature, an organ with an organ, instead of an organ with its function. In this case, it would be possible to proceed little by little to a solution more and more plausible, and there would be the more chance of a successful issue the more resolutely we a.s.sumed the evolutionist hypothesis.

Let us place side by side the eye of a vertebrate and that of a mollusc such as the common Pecten. We find the same essential parts in each, composed of a.n.a.logous elements. The eye of the Pecten presents a retina, a cornea, a lens of cellular structure like our own. There is even that peculiar inversion of retinal elements which is not met with, in general, in the retina of the invertebrates. Now, the origin of molluscs may be a debated question, but, whatever opinion we hold, all are agreed that molluscs and vertebrates separated from their common parent-stem long before the appearance of an eye so complex as that of the Pecten.

Whence, then, the structural a.n.a.logy?

Let us question on this point the two opposed systems of evolutionist explanation in turn--the hypothesis of purely accidental variations, and that of a variation directed in a definite way under the influence of external conditions.

The first, as is well known, is presented to-day in two quite different forms. Darwin spoke of very slight variations being acc.u.mulated by natural selection. He was not ignorant of the facts of sudden variation; but he thought these "sports," as he called them, were only monstrosities incapable of perpetuating themselves; and he accounted for the genesis of species by an acc.u.mulation of _insensible_ variations.[26] Such is still the opinion of many naturalists. It is tending, however, to give way to the opposite idea that a new species comes into being all at once by the simultaneous appearance of several new characters, all somewhat different from the previous ones. This latter hypothesis, already proposed by various authors, notably by Bateson in a remarkable book,[27] has become deeply significant and acquired great force since the striking experiments of Hugo de Vries.

This botanist, working on the _OEnothera Lamarckiana_, obtained at the end of a few generations a certain number of new species. The theory he deduces from his experiments is of the highest interest. Species pa.s.s through alternate periods of stability and transformation. When the period of "mutability" occurs, unexpected forms spring forth in a great number of different directions.[28]--We will not attempt to take sides between this hypothesis and that of insensible variations. Indeed, perhaps both are partly true. We wish merely to point out that if the variations invoked are accidental, they do not, whether small or great, account for a similarity of structure such as we have cited.

Let us a.s.sume, to begin with, the Darwinian theory of insensible variations, and suppose the occurrence of small differences due to chance, and continually acc.u.mulating. It must not be forgotten that all the parts of an organism are necessarily coordinated. Whether the function be the effect of the organ or its cause, it matters little; one point is certain--the organ will be of no use and will not give selection a hold unless it functions. However the minute structure of the retina may develop, and however complicated it may become, such progress, instead of favoring vision, will probably hinder it if the visual centres do not develop at the same time, as well as several parts of the visual organ itself. If the variations are accidental, how can they ever agree to arise in every part of the organ at the same time, in such way that the organ will continue to perform its function? Darwin quite understood this; it is one of the reasons why he regarded variation as insensible.[29] For a difference which arises accidentally at one point of the visual apparatus, if it be very slight, will not hinder the functioning of the organ; and hence this first accidental variation can, in a sense, _wait for_ complementary variations to acc.u.mulate and raise vision to a higher degree of perfection. Granted; but while the insensible variation does not hinder the functioning of the eye, neither does it help it, so long as the variations that are complementary do not occur. How, in that case, can the variation be retained by natural selection? Unwittingly one will reason as if the slight variation were a toothing stone set up by the organism and reserved for a later construction. This hypothesis, so little conformable to the Darwinian principle, is difficult enough to avoid even in the case of an organ which has been developed along one single main line of evolution, _e.g._ the vertebrate eye. But it is absolutely forced upon us when we observe the likeness of structure of the vertebrate eye and that of the molluscs. How could the same small variations, incalculable in number, have ever occurred in the same order on two independent lines of evolution, if they were purely accidental? And how could they have been preserved by selection and acc.u.mulated in both cases, the same in the same order, when each of them, taken separately, was of no use?

Let us turn, then, to the hypothesis of sudden variations, and see whether it will solve the problem. It certainly lessens the difficulty on one point, but it makes it much worse on another. If the eye of the mollusc and that of the vertebrate have both been raised to their present form by a relatively small number of sudden leaps, I have less difficulty in understanding the resemblance of the two organs than if this resemblance were due to an incalculable number of infinitesimal resemblances acquired successively: in both cases it is chance that operates, but in the second case chance is not required to work the miracle it would have to perform in the first. Not only is the number of resemblances to be added somewhat reduced, but I can also understand better how each could be preserved and added to the others; for the elementary variation is now considerable enough to be an advantage to the living being, and so to lend itself to the play of selection. But here there arises another problem, no less formidable, viz., how do all the parts of the visual apparatus, suddenly changed, remain so well coordinated that the eye continues to exercise its function? For the change of one part alone will make vision impossible, unless this change is absolutely infinitesimal. The parts must then all change at once, each consulting the others. I agree that a great number of uncoordinated variations may indeed have arisen in less fortunate individuals, that natural selection may have eliminated these, and that only the combination fit to endure, capable of preserving and improving vision, has survived. Still, this combination had to be produced. And, supposing chance to have granted this favor once, can we admit that it repeats the self-same favor in the course of the history of a species, so as to give rise, every time, all at once, to new complications marvelously regulated with reference to each other, and so related to former complications as to go further on in the same direction? How, especially, can we suppose that by a series of mere "accidents" these sudden variations occur, the same, in the same order,--involving in each case a perfect harmony of elements more and more numerous and complex--along two independent lines of evolution?

The law of correlation will be invoked, of course; Darwin himself appealed to it.[30] It will be alleged that a change is not localized in a single point of the organism, but has its necessary recoil on other points. The examples cited by Darwin remain cla.s.sic: white cats with blue eyes are generally deaf; hairless dogs have imperfect dent.i.tion, etc.--Granted; but let us not play now on the word "correlation." A collective whole of _solidary_ changes is one thing, a system of _complementary_ changes--changes so coordinated as to keep up and even improve the functioning of an organ under more complicated conditions--is another. That an anomaly of the pilous system should be accompanied by an anomaly of dent.i.tion is quite conceivable without our having to call for a special principle of explanation; for hair and teeth are similar formations,[31] and the same chemical change of the germ that hinders the formation of hair would probably obstruct that of teeth: it may be for the same sort of reason that white cats with blue eyes are deaf. In these different examples the "correlative" changes are only _solidary_ changes (not to mention the fact that they are really _lesions_, namely, diminutions or suppressions, and not additions, which makes a great difference). But when we speak of "correlative" changes occurring suddenly in the different parts of the eye, we use the word in an entirely new sense: this time there is a whole set of changes not only simultaneous, not only bound together by community of origin, but so coordinated that the organ keeps on performing the same simple function, and even performs it better. That a change in the germ, which influences the formation of the retina, may affect at the same time also the formation of the cornea, the iris, the lens, the visual centres, etc., I admit, if necessary, although they are formations that differ much more from one another in their original nature than do probably hair and teeth. But that all these simultaneous changes should occur in such a way as to improve or even merely maintain vision, this is what, in the hypothesis of sudden variation, I cannot admit, unless a mysterious principle is to come in, whose duty it is to watch over the interest of the function. But this would be to give up the idea of "accidental" variation. In reality, these two senses of the word "correlation" are often interchanged in the mind of the biologist, just like the two senses of the word "adaptation." And the confusion is almost legitimate in botany, that science in which the theory of the formation of species by sudden variation rests on the firmest experimental basis. In vegetables, function is far less narrowly bound to form than in animals. Even profound morphological differences, such as a change in the form of leaves, have no appreciable influence on the exercise of function, and so do not require a whole system of complementary changes for the plant to remain fit to survive. But it is not so in the animal, especially in the case of an organ like the eye, a very complex structure and very delicate function. Here it is impossible to identify changes that are simply solidary with changes which are also complementary. The two senses of the word "correlation" must be carefully distinguished; it would be a downright paralogism to adopt one of them in the premisses of the reasoning, and the other in the conclusion. And this is just what is done when the principle of correlation is invoked in explanations of _detail_ in order to account for complementary variations, and then correlation _in general_ is spoken of as if it were any group of variations provoked by any variation of the germ. Thus, the notion of correlation is first used in current science as it might be used by an advocate of finality; it is understood that this is only a convenient way of expressing oneself, that one will correct it and fall back on pure mechanism when explaining the nature of the principles and turning from science to philosophy. And one does then come back to pure mechanism, but only by giving a new meaning to the word "correlation"--a meaning which would now make correlation inapplicable to the detail it is called upon to explain.

To sum up, if the accidental variations that bring about evolution are insensible variations, some good genius must be appealed to--the genius of the future species--in order to preserve and acc.u.mulate these variations, for selection will not look after this. If, on the other hand, the accidental variations are sudden, then, for the previous function to go on or for a new function to take its place, all the changes that have happened together must be complementary. So we have to fall back on the good genius again, this time to obtain the _convergence_ of _simultaneous_ changes, as before to be a.s.sured of the _continuity of direction_ of _successive_ variations. But in neither case can parallel development of the same complex structures on independent lines of evolution be due to a mere acc.u.mulation of accidental variations. So we come to the second of the two great hypotheses we have to examine. Suppose the variations are due, not to accidental and inner causes, but to the direct influence of outer circ.u.mstances. Let us see what line we should have to take, on this hypothesis, to account for the resemblance of eye-structure in two series that are independent of each other from the phylogenetic point of view.

Though molluscs and vertebrates have evolved separately, both have remained exposed to the influence of light. And light is a physical cause bringing forth certain definite effects. Acting in a continuous way, it has been able to produce a continuous variation in a constant direction. Of course it is unlikely that the eye of the vertebrate and that of the mollusc have been built up by a series of variations due to simple chance. Admitting even that light enters into the case as an instrument of selection, in order to allow only useful variations to persist, there is no possibility that the play of chance, even thus supervised from without, should bring about in both cases the same juxtaposition of elements coordinated in the same way. But it would be different supposing that light acted directly on the organized matter so as to change its structure and somehow adapt this structure to its own form. The resemblance of the two effects would then be explained by the ident.i.ty of the cause. The more and more complex eye would be something like the deeper and deeper imprint of light on a matter which, being organized, possesses a special apt.i.tude for receiving it.

But can an organic structure be likened to an imprint? We have already called attention to the ambiguity of the term "adaptation." The gradual complication of a form which is being better and better adapted to the mold of outward circ.u.mstances is one thing, the increasingly complex structure of an instrument which derives more and more advantage from these circ.u.mstances is another. In the former case, the matter merely receives an imprint; in the second, it reacts positively, it solves a problem. Obviously it is this second sense of the word "adapt" that is used when one says that the eye has become better and better adapted to the influence of light. But one pa.s.ses more or less unconsciously from this sense to the other, and a purely mechanistic biology will strive to make the _pa.s.sive_ adaptation of an inert matter, which submits to the influence of its environment, mean the same as the _active_ adaptation of an organism which derives from this influence an advantage it can appropriate. It must be owned, indeed, that Nature herself appears to invite our mind to confuse these two kinds of adaptation, for she usually begins by a pa.s.sive adaptation where, later on, she will build up a mechanism for active response. Thus, in the case before us, it is unquestionable that the first rudiment of the eye is found in the pigment-spot of the lower organisms; this spot may indeed have been produced physically, by the mere action of light, and there are a great number of intermediaries between the simple spot of pigment and a complicated eye like that of the vertebrates.--But, from the fact that we pa.s.s from one thing to another by degrees, it does not follow that the two things are of the same nature. From the fact that an orator falls in, at first, with the pa.s.sions of his audience in order to make himself master of them, it will not be concluded that to _follow_ is the same as to _lead_. Now, living matter seems to have no other means of turning circ.u.mstances to good account than by adapting itself to them pa.s.sively at the outset. Where it has to direct a movement, it begins by adopting it. Life proceeds by insinuation. The intermediate degrees between a pigment-spot and an eye are nothing to the point: however numerous the degrees, there will still be the same interval between the pigment-spot and the eye as between a photograph and a photographic apparatus. Certainly the photograph has been gradually turned into a photographic apparatus; but could light alone, a physical force, ever have provoked this change, and converted an impression left by it into a machine capable of using it?

It may be claimed that considerations of utility are out of place here; that the eye is not made to see, but that we see because we have eyes; that the organ is what it is, and "utility" is a word by which we designate the functional effects of the structure. But when I say that the eye "makes use of" light, I do not merely mean that the eye is capable of seeing; I allude to the very precise relations that exist between this organ and the apparatus of locomotion. The retina of vertebrates is prolonged in an optic nerve, which, again, is continued by cerebral centres connected with motor mechanisms. Our eye makes use of light in that it enables us to utilize, by movements of reaction, the objects that we see to be advantageous, and to avoid those which we see to be injurious. Now, of course, as light may have produced a pigment-spot by physical means, so it can physically determine the movements of certain organisms; ciliated Infusoria, for instance, react to light. But no one would hold that the influence of light has physically caused the formation of a nervous system, of a muscular system, of an osseous system, all things which are continuous with the apparatus of vision in vertebrate animals. The truth is, when one speaks of the gradual formation of the eye, and, still more, when one takes into account all that is inseparably connected with it, one brings in something entirely different from the direct action of light. One implicitly attributes to organized matter a certain capacity _sui generis_, the mysterious power of building up very complicated machines to utilize the simple excitation that it undergoes.

But this is just what is claimed to be unnecessary. Physics and chemistry are said to give us the key to everything. Eimer's great work is instructive in this respect. It is well known what persevering effort this biologist has devoted to demonstrating that transformation is brought about by the influence of the external on the internal, continuously exerted in the same direction, and not, as Darwin held, by accidental variations. His theory rests on observations of the highest interest, of which the starting-point was the study of the course followed by the color variation of the skin in certain lizards. Before this, the already old experiments of Dorfmeister had shown that the same chrysalis, according as it was submitted to cold or heat, gave rise to very different b.u.t.terflies, which had long been regarded as independent species, _Vanessa levana_ and _Vanessa prorsa_: an intermediate temperature produces an intermediate form. We might cla.s.s with these facts the important transformations observed in a little crustacean, _Artemia salina_, when the salt of the water it lives in is increased or diminished.[32] In these various experiments the external agent seems to act as a cause of transformation. But what does the word "cause" mean here? Without undertaking an exhaustive a.n.a.lysis of the idea of causality, we will merely remark that three very different meanings of this term are commonly confused. A cause may act by _impelling_, _releasing_, or _unwinding_. The billiard-ball, that strikes another, determines its movement by _impelling_. The spark that explodes the powder acts by _releasing_. The gradual relaxing of the spring, that makes the phonograph turn, _unwinds_ the melody inscribed on the cylinder: if the melody which is played be the effect, and the relaxing of the spring the cause, we must say that the cause acts by _unwinding_.

What distinguishes these three cases from each other is the greater or less solidarity between the cause and the effect. In the first, the quant.i.ty and quality of the effect vary with the quant.i.ty and quality of the cause. In the second, neither quality nor quant.i.ty of the effect varies with quality and quant.i.ty of the cause: the effect is invariable.

In the third, the quant.i.ty of the effect depends on the quant.i.ty of the cause, but the cause does not influence the quality of the effect: the longer the cylinder turns by the action of the spring, the more of the melody I shall hear, but the nature of the melody, or of the part heard, does not depend on the action of the spring. Only in the first case, really, does cause _explain_ effect; in the others the effect is more or less given in advance, and the antecedent invoked is--in different degrees, of course--its occasion rather than its cause. Now, in saying that the saltness of the water is the cause of the transformations of Artemia, or that the degree of temperature determines the color and marks of the wings which a certain chrysalis will a.s.sume on becoming a b.u.t.terfly, is the word "cause" used in the first sense? Obviously not: causality has here an intermediary sense between those of unwinding and releasing. Such, indeed, seems to be Eimer's own meaning when he speaks of the "kaleidoscopic" character of the variation,[33] or when he says that the variation of organized matter works in a definite way, just as inorganic matter crystallizes in definite directions.[34] And it may be granted, perhaps, that the process is a merely physical and chemical one in the case of the color-changes of the skin. But if this sort of explanation is extended to the case of the gradual formation of the eye of the vertebrate, for instance, it must be supposed that the physico-chemistry of living bodies is such that the influence of light has caused the organism to construct a progressive series of visual apparatus, all extremely complex, yet all capable of seeing, and of seeing better and better.[35] What more could the most confirmed finalist say, in order to mark out so exceptional a physico-chemistry?

And will not the position of a mechanistic philosophy become still more difficult, when it is pointed out to it that the egg of a mollusc cannot have the same chemical composition as that of a vertebrate, that the organic substance which evolved toward the first of these two forms could not have been chemically identical with that of the substance which went in the other direction, and that, nevertheless, under the influence of light, the same organ has been constructed in the one case as in the other?

The more we reflect upon it, the more we shall see that this production of the same effect by two different acc.u.mulations of an enormous number of small causes is contrary to the principles of mechanistic philosophy.

We have concentrated the full force of our discussion upon an example drawn from phylogenesis. But ontogenesis would have furnished us with facts no less cogent. Every moment, right before our eyes, nature arrives at identical results, in sometimes neighboring species, by entirely different embryogenic processes. Observations of "heteroblastia" have multiplied in late years,[36] and it has been necessary to reject the almost cla.s.sical theory of the specificity of embryonic gills. Still keeping to our comparison between the eye of vertebrates and that of molluscs, we may point out that the retina of the vertebrate is produced by an expansion in the rudimentary brain of the young embryo. It is a regular nervous centre which has moved toward the periphery. In the mollusc, on the contrary, the retina is derived from the ectoderm directly, and not indirectly by means of the embryonic encephalon. Quite different, therefore, are the evolutionary processes which lead, in man and in the Pecten, to the development of a like retina. But, without going so far as to compare two organisms so distant from each other, we might reach the same conclusion simply by looking at certain very curious facts of regeneration in one and the same organism.

If the crystalline lens of a Triton be removed, it is regenerated by the iris.[37] Now, the original lens was built out of the ectoderm, while the iris is of mesodermic origin. What is more, in the _Salamandra maculata_, if the lens be removed and the iris left, the regeneration of the lens takes place at the upper part of the iris; but if this upper part of the iris itself be taken away, the regeneration takes place in the inner or retinal layer of the remaining region.[38] Thus, parts differently situated, differently const.i.tuted, meant normally for different functions, are capable of performing the same duties and even of manufacturing, when necessary, the same pieces of the machine. Here we have, indeed, the same effect obtained by different combinations of causes.

Whether we will or no, we must appeal to some inner directing principle in order to account for this convergence of effects. Such convergence does not appear possible in the Darwinian, and especially the neo-Darwinian, theory of insensible accidental variations, nor in the hypothesis of sudden accidental variations, nor even in the theory that a.s.signs definite directions to the evolution of the various organs by a kind of mechanical composition of the external with the internal forces.

So we come to the only one of the present forms of evolution which remains for us to mention, viz., neo-Lamarckism.

It is well known that Lamarck attributed to the living being the power of varying by use or disuse of its organs, and also of pa.s.sing on the variation so acquired to its descendants. A certain number of biologists hold a doctrine of this kind to-day. The variation that results in a new species is not, they believe, merely an accidental variation inherent in the germ itself, nor is it governed by a determinism _sui generis_ which develops definite characters in a definite direction, apart from every consideration of utility. It springs from the very effort of the living being to adapt itself to the circ.u.mstances of its existence. The effort may indeed be only the mechanical exercise of certain organs, mechanically elicited by the pressure of external circ.u.mstances. But it may also imply consciousness and will, and it is in this sense that it appears to be understood by one of the most eminent representatives of the doctrine, the American naturalist Cope.[39] Neo-Lamarckism is therefore, of all the later forms of evolutionism, the only one capable of admitting an internal and psychological principle of development, although it is not bound to do so. And it is also the only evolutionism that seems to us to account for the building up of identical complex organs on independent lines of development. For it is quite conceivable that the same effort to turn the same circ.u.mstances to good account might have the same result, especially if the problem put by the circ.u.mstances is such as to admit of only one solution. But the question remains, whether the term "effort" must not then be taken in a deeper sense, a sense even more psychological than any neo-Lamarckian supposes.

For a mere variation of size is one thing, and a change of form is another. That an organ can be strengthened and grow by exercise, n.o.body will deny. But it is a long way from that to the progressive development of an eye like that of the molluscs and of the vertebrates. If this development be ascribed to the influence of light, long continued but pa.s.sively received, we fall back on the theory we have just criticized.

If, on the other hand, an internal activity is appealed to, then it must be something quite different from what we usually call an effort, for never has an effort been known to produce the slightest complication of an organ, and yet an enormous number of complications, all admirably coordinated, have been necessary to pa.s.s from the pigment-spot of the Infusorian to the eye of the vertebrate. But, even if we accept this notion of the evolutionary process in the case of animals, how can we apply it to plants? Here, variations of form do not seem to imply, nor always to lead to, functional changes; and even if the cause of the variation is of a psychological nature, we can hardly call it an effort, unless we give a very unusual extension to the meaning of the word. The truth is, it is necessary to dig beneath the effort itself and look for a deeper cause.

This is especially necessary, we believe, if we wish to get at a cause of regular hereditary variations. We are not going to enter here into the controversies over the transmissibility of acquired characters; still less do we wish to take too definite a side on this question, which is not within our province. But we cannot remain completely indifferent to it. Nowhere is it clearer that philosophers can not to-day content themselves with vague generalities, but must follow the scientists in experimental detail and discuss the results with them. If Spencer had begun by putting to himself the question of the hereditability of acquired characters, his evolutionism would no doubt have taken an altogether different form. If (as seems probable to us) a habit contracted by the individual were transmitted to its descendants only in very exceptional cases, all the Spencerian psychology would need remaking, and a large part of Spencer's philosophy would fall to pieces.

Let us say, then, how the problem seems to us to present itself, and in what direction an attempt might be made to solve it.

After having been affirmed as a dogma, the transmissibility of acquired characters has been no less dogmatically denied, for reasons drawn _a priori_ from the supposed nature of germinal cells. It is well known how Weismann was led, by his hypothesis 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 apt.i.tude, which existed prior to the habit. This apt.i.tude 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 pa.s.sed 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 a.s.sured 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-Sequard, repeated and confirmed by other physiologists.[41] By cutting the spinal cord or the sciatic nerve of guinea-pigs, Brown-Sequard 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-Sequard 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 s.e.xual elements.[42] This objection has been answered by Brown-Sequard 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-Sequard correspond to the formation of precisely this convulsion-causing poison. If so, the toxin pa.s.sed 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 a.n.a.logous process, on the spermatozoa and the ova.[47] To conclude, then: the inheritance of an acquired peculiarity in the experiments of Brown-Sequard 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 pa.s.ses 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 a.s.sume 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 acc.u.mulated before the pa.s.sage 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.

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 pa.s.ses 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 a.s.serts 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 _OEnothera 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 a