SigPhi · Henri Bergson

Creative Evolution

Page 8 of 27

from the air and earth and water. But now we come to another difference, deeper than this, though not unconnected with it.

The animal, being unable to fix directly the carbon and nitrogen which are everywhere to be found, has to seek for its nourishment vegetables which have already fixed these elements, or animals which have taken them from the vegetable kingdom. So the animal must be able to move. From the amoeba, which thrusts out its pseudopodia at random to seize the organic matter scattered in a drop of water, up to the higher animals which have sense-organs with which to recognize their prey, locomotor organs to go and seize it, and a nervous system to coördinate their movements with their sensations, animal life is characterized, in its general direction, by mobility in space. In its most rudimentary form, the animal is a tiny mass of protoplasm enveloped at most in a thin albuminous pellicle which allows full freedom for change of shape and movement. The vegetable cell, on the contrary, is surrounded by a membrane of cellulose, which condemns it to immobility. And, from the bottom to the top of the vegetable kingdom, there are the same habits growing more and more sedentary, the plant having no need to move, and finding around it, in the air and water and soil in which it is placed, the mineral elements it can appropriate directly. It is true that phenomena of movement are seen in plants. Darwin has written a well-known work on the movements of climbing plants. He studied also the contrivances of certain insectivorous plants, such as the Drosera and the Dionaea, to seize their prey. The leaf-movements of the acacia, the sensitive plant, etc., are well known. Moreover, the circulation of the vegetable protoplasm within its sheath bears witness to its relationship to the protoplasm of animals, whilst in a large number of animal species (generally parasites) phenomena of fixation, analogous to those of vegetables, can be observed.[53] Here, again, it would be a mistake to claim that fixity and mobility are the two characters which enable us to decide, by simple inspection alone, whether we have before us a plant or an animal. But fixity, in the animal, generally seems like a torpor into which the species has fallen, a refusal to evolve further in a certain direction; it is closely akin to parasitism and is accompanied by features that recall those of vegetable life. On the other hand, the movements of vegetables have neither the frequency nor the variety of those of animals. Generally, they involve only part of the organism and scarcely ever extend to the whole. In the exceptional cases in which a vague spontaneity appears in vegetables, it is as if we beheld the accidental awakening of an activity normally asleep. In short, although both mobility and fixity exist in the vegetable as in the animal world, the balance is clearly in favor of fixity in the one case and of mobility in the other. These two opposite tendencies are so plainly directive of the two evolutions that the two kingdoms might almost be defined by them. But fixity and mobility, again, are only superficial signs of tendencies that are still deeper.

Between mobility and consciousness there is an obvious relationship. No doubt, the consciousness of the higher organisms seems bound up with certain cerebral arrangements. The more the nervous system develops, the more numerous and more precise become the movements among which it can choose; the clearer, also, is the consciousness that accompanies them. But neither this mobility nor this choice nor consequently this consciousness involves as a necessary condition the presence of a nervous system; the latter has only canalized in definite directions, and brought up to a higher degree of intensity, a rudimentary and vague activity, diffused throughout the mass of the organized substance. The lower we descend in the animal series, the more the nervous centres are simplified, and the more, too, they separate from each other, till finally the nervous elements disappear, merged in the mass of a less differentiated organism. But it is the same with all the other apparatus, with all the other anatomical elements; and it would be as absurd to refuse consciousness to an animal because it has no brain as to declare it incapable of nourishing itself because it has no stomach. The truth is that the nervous system arises, like the other systems, from a division of labor. It does not create the function, it only brings it to a higher degree of intensity and precision by giving it the double form of reflex and voluntary activity. To accomplish a true reflex movement, a whole mechanism is necessary, set up in the spinal cord or the medulla. To choose voluntarily between several definite courses of action, cerebral centres are necessary, that is, crossways from which paths start, leading to motor mechanisms of diverse form but equal precision. But where nervous elements are not yet canalized, still less concentrated into a system, there is something from which, by a kind of splitting, both the reflex and the voluntary will arise, something which has neither the mechanical precision of the former nor the intelligent hesitations of the latter, but which, partaking of both it may be infinitesimally, is a reaction simply undecided, and therefore vaguely conscious. This amounts to saying that the humblest organism is conscious in proportion to its power to move _freely_. Is consciousness here, in relation to movement, the effect or the cause? In one sense it is the cause, since it has to direct locomotion. But in another sense it is the effect; for it is the motor activity that maintains it, and, once this activity disappears, consciousness dies away or rather falls asleep. In crustaceans such as the rhizocephala, which must formerly have shown a more differentiated structure, fixity and parasitism accompany the degeneration and almost complete disappearance of the nervous system. Since, in such a case, the progress of organization must have localized all the conscious activity in nervous centres, we may conjecture that consciousness is even weaker in animals of this kind than in organisms much less differentiated, which have never had nervous centres but have remained mobile.

How then could the plant, which is fixed in the earth and finds its food on the spot, have developed in the direction of conscious activity? The membrane of cellulose, in which the protoplasm wraps itself up, not only prevents the simplest vegetable organism from moving, but screens it also, in some measure, from those outer stimuli which act on the sensibility of the animal as irritants and prevent it from going to sleep.[54] The plant is therefore unconscious. Here again, however, we must beware of radical distinctions. "Unconscious" and "conscious" are not two labels which can be mechanically fastened, the one on every vegetable cell, the other on all animals. While consciousness sleeps in the animal which has degenerated into a motionless parasite, it probably awakens in the vegetable that has regained liberty of movement, and awakens in just the degree to which the vegetable has reconquered this liberty. Nevertheless, consciousness and unconsciousness mark the directions in which the two kingdoms have developed, in this sense, that to find the best specimens of consciousness in the animal we must _ascend_ to the highest representatives of the series, whereas, to find probable cases of vegetable consciousness, we must _descend_ as low as possible in the scale of plants--down to the zoospores of the algae, for instance, and, more generally, to those unicellular organisms which may be said to hesitate between the vegetable form and animality. From this standpoint, and in this measure, we should define the animal by sensibility and awakened consciousness, the vegetable by consciousness asleep and by insensibility.

To sum up, the vegetable manufactures organic substances directly with mineral substances; as a rule, this aptitude enables it to dispense with movement and so with feeling. Animals, which are obliged to go in search of their food, have evolved in the direction of locomotor activity, and consequently of a consciousness more and more distinct, more and more ample.

* * * * * Now, it seems to us most probable that the animal cell and the vegetable cell are derived from a common stock, and that the first living organisms oscillated between the vegetable and animal form, participating in both at once. Indeed, we have just seen that the characteristic tendencies of the evolution of the two kingdoms, although divergent, coexist even now, both in the plant and in the animal. The proportion alone differs. Ordinarily, one of the two tendencies covers or crushes down the other, but in exceptional circumstances the suppressed one starts up and regains the place it had lost. The mobility and consciousness of the vegetable cell are not so sound asleep that they cannot rouse themselves when circumstances permit or demand it; and, on the other hand, the evolution of the animal kingdom has always been retarded, or stopped, or dragged back, by the tendency it has kept toward the vegetative life. However full, however overflowing the activity of an animal species may appear, torpor and unconsciousness are always lying in wait for it. It keeps up its rôle only by effort, at the price of fatigue. Along the route on which the animal has evolved, there have been numberless shortcomings and cases of decay, generally associated with parasitic habits; they are so many shuntings on to the vegetative life. Thus, everything bears out the belief that vegetable and animal are descended from a common ancestor which united the tendencies of both in a rudimentary state.

But the two tendencies mutually implied in this rudimentary form became dissociated as they grew. Hence the world of plants with its fixity and insensibility, hence the animals with their mobility and consciousness. There is no need, in order to explain this dividing into two, to bring in any mysterious force. It is enough to point out that the living being leans naturally toward what is most convenient to it, and that vegetables and animals have chosen two different kinds of convenience in the way of procuring the carbon and nitrogen they need. Vegetables continually and mechanically draw these elements from an environment that continually provides it. Animals, by action that is discontinuous, concentrated in certain moments, and conscious, go to find these bodies in organisms that have already fixed them. They are two different ways of being industrious, or perhaps we may prefer to say, of being idle. For this very reason we doubt whether nervous elements, however rudimentary, will ever be found in the plant. What corresponds in it to the directing will of the animal is, we believe, the direction in which it bends the energy of the solar radiation when it uses it to break the connection of the carbon with the oxygen in carbonic acid. What corresponds in it to the sensibility of the animal is the impressionability, quite of its kind, of its chlorophyl light. Now, a nervous system being pre-eminently a mechanism which serves as intermediary between sensations and volitions, the true "nervous system" of the plant seems to be the mechanism or rather chemicism _sui generis_ which serves as intermediary between the impressionability of its chlorophyl to light and the producing of starch: which amounts to saying that the plant can have no nervous elements, and that _the same impetus that has led the animal to give itself nerves and nerve centres must have ended, in the plant, in the chlorophyllian function_.[55] * * * * * This first glance over the organized world will enable us to ascertain more precisely what unites the two kingdoms, and also what separates them.

Suppose, as we suggested in the preceding chapter, that at the root of life there is an effort to engraft on to the necessity of physical forces the largest possible amount of _indetermination_. This effort cannot result in the creation of energy, or, if it does, the quantity created does not belong to the order of magnitude apprehended by our senses and instruments of measurement, our experience and science. All that the effort can do, then, is to make the best of a pre-existing energy which it finds at its disposal. Now, it finds only one way of succeeding in this, namely, to secure such an accumulation of potential energy from matter, that it can get, at any moment, the amount of work it needs for its action, simply by pulling a trigger. The effort itself possesses only that power of releasing. But the work of releasing, although always the same and always smaller than any given quantity, will be the more effective the heavier the weight it makes fall and the greater the height--or, in other words, the greater the sum of potential energy accumulated and disposable. As a matter of fact, the principal source of energy usable on the surface of our planet is the sun. So the problem was this: to obtain from the sun that it should partially and provisionally suspend, here and there, on the surface of the earth, its continual outpour of usable energy, and store a certain quantity of it, in the form of unused energy, in appropriate reservoirs, whence it could be drawn at the desired moment, at the desired spot, in the desired direction. The substances forming the food of animals are just such reservoirs. Made of very complex molecules holding a considerable amount of chemical energy in the potential state, they are like explosives which only need a spark to set free the energy stored within them. Now, it is probable that life tended at the beginning to compass at one and the same time both the manufacture of the explosive and the explosion by which it is utilized. In this case, the same organism that had directly stored the energy of the solar radiation would have expended it in free movements in space. And for that reason we must presume that the first living beings sought on the one hand to accumulate, without ceasing, energy borrowed from the sun, and on the other hand to expend it, in a discontinuous and explosive way, in movements of locomotion. Even to-day, perhaps, a chlorophyl-bearing Infusorian such as the Euglena may symbolize this primordial tendency of life, though in a mean form, incapable of evolving. Is the divergent development of the two kingdoms related to what one may call the oblivion of each kingdom as regards one of the two halves of the programme? Or rather, which is more likely, was the very nature of the matter, that life found confronting it on our planet, opposed to the possibility of the two tendencies evolving very far together in the same organism? What is certain is that the vegetable has trended principally in the first direction and the animal in the second. But if, from the very first, in making the explosive, nature had for object the explosion, then it is the evolution of the animal, rather than that of the vegetable, that indicates, on the whole, the fundamental direction of life.

The "harmony" of the two kingdoms, the complementary characters they display, might then be due to the fact that they develop two tendencies which at first were fused in one. The more the single original tendency grows, the harder it finds it to keep united in the same living being those two elements which in the rudimentary state implied each other. Hence a parting in two, hence two divergent evolutions; hence also two series of characters opposed in certain points, complementary in others, but, whether opposed or complementary, always preserving an appearance of kinship. While the animal evolved, not without accidents along the way, toward a freer and freer expenditure of discontinuous energy, the plant perfected rather its system of accumulation without moving. We shall not dwell on this second point. Suffice it to say that the plant must have been greatly benefited, in its turn, by a new division, analogous to that between plants and animals. While the primitive vegetable cell had to fix by itself both its carbon and its nitrogen, it became able almost to give up the second of these two functions as soon as microscopic vegetables came forward which leaned in this direction exclusively, and even specialized diversely in this still complicated business. The microbes that fix the nitrogen of the air and those which convert the ammoniacal compounds into nitrous ones, and these again into nitrates, have, by the same splitting up of a tendency primitively one, rendered to the whole vegetable world the same kind of service as the vegetables in general have rendered to animals. If a special kingdom were to be made for these microscopic vegetables, it might be said that in the microbes of the soil, the vegetables and the animals, we have before us the _analysis_, carried out by the matter that life found at its disposal on our planet, of all that life contained, at the outset, in a state of reciprocal implication. Is this, properly speaking, a "division of labor"? These words do not give the exact idea of evolution, such as we conceive it. Wherever there is division of labor, there is _association_ and also _convergence_ of effort. Now, the evolution we are speaking of is never achieved by means of association, but by _dissociation_; it never tends toward convergence, but toward _divergence_ of efforts. The harmony between terms that are mutually complementary in certain points is not, in our opinion, produced, in course of progress, by a reciprocal adaptation; on the contrary, it is complete only at the start. It arises from an original identity, from the fact that the evolutionary process, splaying out like a sheaf, sunders, in proportion to their simultaneous growth, terms which at first completed each other so well that they coalesced.

Now, the elements into which a tendency splits up are far from possessing the same importance, or, above all, the same power to evolve. We have just distinguished three different kingdoms, if one may so express it, in the organized world. While the first comprises only microorganisms which have remained in the rudimentary state, animals and vegetables have taken their flight toward very lofty fortunes. Such, indeed, is generally the case when a tendency divides. Among the divergent developments to which it gives rise, some go on indefinitely, others come more or less quickly to the end of their tether. These latter do not issue directly from the primitive tendency, but from one of the elements into which it has divided; they are residual developments made and left behind on the way by some truly elementary tendency which continues to evolve. Now, these truly elementary tendencies, we think, bear a mark by which they may be recognized.

This mark is like a trace, still visible in each, of what was in the original tendency of which they represent the elementary directions. The elements of a tendency are not like objects set beside each other in space and mutually exclusive, but rather like psychic states, each of which, although it be itself to begin with, yet partakes of others, and so virtually includes in itself the whole personality to which it belongs. There is no real manifestation of life, we said, that does not show us, in a rudimentary or latent state, the characters of other manifestations. Conversely, when we meet, on one line of evolution, a recollection, so to speak, of what is developed along other lines, we must conclude that we have before us dissociated elements of one and the same original tendency. In this sense, vegetables and animals represent the two great divergent developments of life. Though the plant is distinguished from the animal by fixity and insensibility, movement and consciousness sleep in it as recollections which may waken. But, beside these normally sleeping recollections, there are others awake and active, just those, namely, whose activity does not obstruct the development of the elementary tendency itself. We may then formulate this law: _When a tendency splits up in the course of its development, each of the special tendencies which thus arise tries to preserve and develop everything in the primitive tendency that is not incompatible with the work for which it is specialized._ This explains precisely the fact we dwelt on in the preceding chapter, viz., the formation of identical complex mechanisms on independent lines of evolution. Certain deep-seated analogies between the animal and the vegetable have probably no other cause: sexual generation is perhaps only a luxury for the plant, but to the animal it was a necessity, and the plant must have been driven to it by the same impetus which impelled the animal thereto, a primitive, original impetus, anterior to the separation of the two kingdoms. The same may be said of the tendency of the vegetable towards a growing complexity. This tendency is essential to the animal kingdom, ever tormented by the need of more and more extended and effective action. But the vegetable, condemned to fixity and insensibility, exhibits the same tendency only because it received at the outset the same impulsion. Recent experiments show that it varies at random when the period of "mutation" arrives; whereas the animal must have evolved, we believe, in much more definite directions. But we will not dwell further on this original doubling of the modes of life. Let us come to the evolution of animals, in which we are more particularly interested.

What constitutes animality, we said, is the faculty of utilizing a releasing mechanism for the conversion of as much stored-up potential energy as possible into "explosive" actions. In the beginning the explosion is haphazard, and does not choose its direction. Thus the amoeba thrusts out its pseudopodic prolongations in all directions at once. But, as we rise in the animal scale, the form of the body itself is observed to indicate a certain number of very definite directions along which the energy travels. These directions are marked by so many chains of nervous elements. Now, the nervous element has gradually emerged from the barely differentiated mass of organized tissue. It may, therefore, be surmised that in the nervous element, as soon as it appears, and also in its appendages, the faculty of suddenly freeing the gradually stored-up energy is concentrated. No doubt, every living cell expends energy without ceasing, in order to maintain its equilibrium. The vegetable cell, torpid from the start, is entirely absorbed in this work of maintenance alone, as if it took for end what must at first have been only a means. But, in the animal, all points to action, that is, to the utilization of energy for movements from place to place. True, every animal cell expends a good deal--often the whole--of the energy at its disposal in keeping itself alive; but the organism as a whole tries to attract as much energy as possible to those points where the locomotive movements are effected. So that where a nervous system exists, with its complementary sense-organs and motor apparatus, everything should happen as if the rest of the body had, as its essential function, to prepare for these and pass on to them, at the moment required, that force which they are to liberate by a sort of explosion.

The part played by food amongst the higher animals is, indeed, extremely complex. In the first place it serves to repair tissues, then it provides the animal with the heat necessary to render it as independent as possible of changes in external temperature. Thus it preserves, supports, and maintains the organism in which the nervous system is set and on which the nervous elements have to live. But these nervous elements would have no reason for existence if the organism did not pass to them, and especially to the muscles they control, a certain energy to expend; and it may even be conjectured that there, in the main, is the essential and ultimate destination of food. This does not mean that the greater part of the food is used in this work. A state may have to make enormous expenditure to secure the return of taxes, and the sum which it will have to dispose of, after deducting the cost of collection, will perhaps be very small: that sum is, none the less, the reason for the tax and for all that has been spent to obtain its return. So it is with the energy which the animal demands of its food.

Many facts seem to indicate that the nervous and muscular elements stand in this relation towards the rest of the organism. Glance first at the distribution of alimentary substances among the different elements of the living body. These substances fall into two classes, one the quaternary or albuminoid, the other the ternary, including the carbohydrates and the fats. The albuminoids are properly plastic, destined to repair the tissues--although, owing to the carbon they contain, they are capable of providing energy on occasion. But the function of supplying energy has devolved more particularly on the second class of substances: these, being deposited in the cell rather than forming part of its substance, convey to it, in the form of chemical potential, an expansive energy that may be directly converted into either movement or heat. In short, the chief function of the albuminoids is to repair the machine, while the function of the other class of substances is to supply power. It is natural that the albuminoids should have no specially allotted destination, since every part of the machine has to be maintained. But not so with the other substances. The carbohydrates are distributed very unequally, and this inequality of distribution seems to us in the highest degree instructive.

Conveyed by the arterial blood in the form of glucose, these substances are deposited, in the form of glycogen, in the different cells forming the tissues. We know that one of the principal functions of the liver is to maintain at a constant level the quantity of glucose held by the blood, by means of the reserves of glycogen secreted by the hepatic cells. Now, in this circulation of glucose and accumulation of glycogen, it is easy to see that the effect is as if the whole effort of the organism were directed towards providing with potential energy the elements of both the muscular and the nervous tissues. The organism proceeds differently in the two cases, but it arrives at the same result. In the first case, it provides the muscle-cell with a large reserve deposited in advance: the quantity of glycogen contained in the muscles is, indeed, enormous in comparison with what is found in the other tissues. In the nervous tissue, on the contrary, the reserve is small (the nervous elements, whose function is merely to liberate the potential energy stored in the muscle, never have to furnish much work at one time); but the remarkable thing is that this reserve is restored by the blood at the very moment that it is expended, so that the nerve is instantly recharged with potential energy. Muscular tissue and nervous tissue are, therefore, both privileged, the one in that it is stocked with a large reserve of energy, the other in that it is always served at the instant it is in need and to the exact extent of its requirements.