Creative Evolution

Indeed, if the fringe exists, however delicate and indistinct, it should have more importance for philosophy than the bright nucleus it surrounds. For it is its presence that enables us to affirm that the nucleus is a nucleus, that pure intellect is a contraction, by condensation, of a more extensive power. And, just because this vague intuition is of no help in directing our action on things, which action takes place exclusively on the surface of reality, we may presume that it is to be exercised not merely on the surface, but below.

As soon as we go out of the encasings in which radical mechanism and radical finalism confine our thought, reality appears as a ceaseless upspringing of something new, which has no sooner arisen to make the present than it has already fallen back into the past; at this exact moment it falls under the glance of the intellect, whose eyes are ever turned to the rear. This is already the case with our inner life. For each of our acts we shall easily find antecedents of which it may in some sort be said to be the mechanical resultant. And it may equally well be said that each action is the realization of an intention. In this sense mechanism is everywhere, and finality everywhere, in the evolution of our conduct. But if our action be one that involves the whole of our person and is truly ours, it could not have been foreseen, even though its antecedents explain it when once it has been accomplished. And though it be the realizing of an intention, it differs, as a present and new reality, from the intention, which can never aim at anything but recommencing or rearranging the past. Mechanism and finalism are therefore, here, only external views of our conduct. They extract its intellectuality. But our conduct slips between them and extends much further. Once again, this does not mean that free action is capricious, unreasonable action.

To behave according to caprice is to oscillate mechanically between two or more ready-made alternatives and at length to settle on one of them; it is no real maturing of an internal state, no real evolution; it is merely—however paradoxical the assertion may seem—bending the will to imitate the mechanism of the intellect. A conduct that is truly our own, on the contrary, is that of a will which does not try to counterfeit intellect, and which, remaining itself—that is to say, evolving—ripens gradually into acts which the intellect will be able to resolve indefinitely into intelligible elements without ever reaching its goal. The free act is incommensurable with the idea, and its "rationality" must be defined by this very incommensurability, which admits the discovery of as much intelligibility within it as we will. Such is the character of our own evolution; and such also, without doubt, that of the evolution of life.

Our reason, incorrigibly presumptuous, imagines itself possessed, by right of birth or by right of conquest, innate or acquired, of all the essential elements of the knowledge of truth. Even where it confesses that it does not know the object presented to it, it believes that its ignorance consists only in not knowing which one of its time-honored categories suits the new object. In what drawer, ready to open, shall we put it? In what garment, already cut out, shall we clothe it? Is it this, or that, or the other thing? And "this," and "that," and "the other thing" are always something already conceived, already known. The idea that for a new object we might have to create a new concept, perhaps a new method of thinking, is deeply repugnant to us. The history of philosophy is there, however, and shows us the eternal conflict of systems, the impossibility of satisfactorily getting the real into the ready-made garments of our ready-made concepts, the necessity of making to measure. But, rather than go to this extremity, our reason prefers to announce once for all, with a proud modesty, that it has to do only with the relative, and that the absolute is not in its province. This preliminary declaration enables it to apply its habitual method of thought without any scruple, and thus, under pretense that it does not touch the absolute, to make absolute judgments upon everything.

Plato was the first to set up the theory that to know the real consists in finding its Idea, that is to say, in forcing it into a pre-existing frame already at our disposal—as if we implicitly possessed universal knowledge. But this belief is natural to the human intellect, always engaged as it is in determining under what former heading it shall catalogue any new object; and it may be said that, in a certain sense, we are all born Platonists.

Nowhere is the inadequacy of this method so obvious as in theories of life. If, in evolving in the direction of the vertebrates in general, of man and intellect in particular, life has had to abandon by the way many elements incompatible with this particular mode of organization and consign them, as we shall show, to other lines of development, it is the totality of these elements that we must find again and rejoin to the intellect proper, in order to grasp the true nature of vital activity. And we shall probably be aided in this by the fringe of vague intuition that surrounds our distinct—that is, intellectual—representation. For what can this useless fringe be, if not that part of the evolving principle which has not shrunk to the peculiar form of our organization, but has settled around it unasked for, unwanted? It is there, accordingly, that we must look for hints to expand the intellectual form of our thought; from there shall we derive the impetus necessary to lift us above ourselves. To form an idea of the whole of life cannot consist in combining simple ideas that have been left behind in us by life itself in the course of its evolution. How could the part be equivalent to the whole, the content to the container, a by-product of the vital operation to the operation itself? Such, however, is our illusion when we define the evolution of life as a "passage from the homogeneous to the heterogeneous," or by any other concept obtained by putting fragments of intellect side by side.

We place ourselves in one of the points where evolution comes to a head—the principal one, no doubt, but not the only one; and there we do not even take all we find, for of the intellect we keep only one or two of the concepts by which it expresses itself; and it is this part of a part that we declare representative of the whole, of something indeed which goes beyond the concrete whole, I mean of the evolution movement of which this "whole" is only the present stage! The truth is, that to represent this the entire intellect would not be too much—nay, it would not be enough. It would be necessary to add to it what we find in every other terminal point of evolution. And these diverse and divergent elements must be considered as so many extracts which are, or at least which were, in their humblest form, mutually complementary. Only then might we have an inkling of the real nature of the evolution movement; and even then we should fail to grasp it completely, for we should still be dealing only with the evolved, which is a result, and not with evolution itself, which is the act by which the result is obtained.

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 mass, 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 identity of impulsion and not to a common aspiration. It would be futile to try to assign 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 passu 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 anticipation of the future. It is a particular mode of viewing the past in the light of the present. In short, the classic 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 fashioned 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 repetitions—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 substituted 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 classic 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.

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 rôle 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 circumstances. 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.

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 accumulation 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 space 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 accumulation 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 accumulation 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 constitutive 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 glass, 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 circumstances it has to live in, where is the pre-existing form awaiting its matter? The circumstances 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 circumstances which are made for it. It will have to make the best of these circumstances, 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 passive, if it is mere repetition 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 surreptitious passing 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 circumstances to the best possible account: then one speaks of adaptation in general as if it were the very impress of circumstances, passively received by an indifferent matter.

But let us come to the examples. It would be interesting first to institute 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 sexuality. 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 sexual 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 quantity of chromatic substance.[22] Yet vegetables and animals have evolved on independent lines, favored by unlike circumstances, 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 circumstances? There is no striking utility in sexual generation; it has been interpreted in the most diverse ways; and some very acute enquirers even regard the sexuality 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 sexual 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 quantity 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 assume the evolutionist hypothesis. Everything is marvelous, indeed, if one consider an eye like ours, in which thousands of elements are coördinated 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 assumed 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 analogous 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 analogy?

The first, as is well known, is presented to-day in two quite different forms. Darwin spoke of very slight variations being accumulated 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 accumulation 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 Œnothera 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 pass 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 assume, to begin with, the Darwinian theory of insensible variations, and suppose the occurrence of small differences due to chance, and continually accumulating. It must not be forgotten that all the parts of an organism are necessarily coördinated. 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 accumulate 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 accumulated 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 coördinated 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 uncoördinated 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 classic: white cats with blue eyes are generally deaf; hairless dogs have imperfect dentition, 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 coördinated 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 dentition 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 coördinated 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 accumulate 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 assured 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 accumulation 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 circumstances. 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 coördinated 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 identity 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 aptitude for receiving it.