CHAPTER III.
OBVERSE À PRIORI PRINCIPLE.

§ 324. When dealing with its phenomena inductively, we saw that however it may be carried on, Genesis “is a process of negative or positive disintegration; and is thus essentially opposed to that process of integration which is the primary process in individual evolution.” (§ 76.) Each new individual, whether separated as a germ or in some more-developed form, is a deduction from the mass of a pre-existing individual or of two pre-existing individuals. Whatever nutritive matter is stored-up along with the germ, if it be deposited in the shape of an egg, is so much nutritive matter lost to the parent. No drop of blood can be absorbed by the fœtus, nor any draught of milk sucked by the young when born, without taking from the mother tissue-forming and force-evolving materials to an equivalent amount. And all subsequent supplies given to progeny, if they are nurtured, involve, to a parent or parents, so much waste in exertion which does not bring its return in assimilated food.

Conversely, the continued aggregation of materials into one organism, renders impossible the formation of other organisms out of those materials. As much assimilated food as is united into a single whole, is so much assimilated food withheld from a plurality of wholes which might else have been produced. Given the absorbed nutriment as a constant quantity, and the longer the building of it up into a concrete shape goes on, the longer must be postponed any building of it up into discrete shapes. And, similarly, the larger the proportion of matter consumed in the functional actions of parents, the smaller must be the proportion of matter which can remain to establish and support the functional actions of offspring.

Though the necessity of these universal relations is tolerably obvious as thus stated generally, it will be useful to dwell for a brief space on their leading aspects.

§ 325. That disintegration which constitutes genesis, may be such as to disperse entirely the aggregate which integration has previously produced—the parent may dissolve wholly into progeny. This dissolution of each aggregate into two or many aggregates, may occur at very short intervals, in which case the bulk attained can be but extremely small; or it may occur at longer intervals, in which case a larger bulk may be attained.

Instead of quickly losing its own individuality in the individualities of its offspring, each member of the race may, after growing for a time, have portions of its substance begin to develop into the parental shape and presently detach themselves; and the parent, maintaining its own identity, may continue indefinitely so to produce young ones. But clearly, the earlier it commences doing this, and the more rapidly it does it, the sooner must the increase of its own bulk be stopped.

Or again, growth and development continuing for a long period without any deduction of materials, an individual of considerable size and organization may result; and then the abstraction of substance for the formation of new individuals, or rather the eggs of them, may be so great that as soon as the eggs are laid the parent dies of exhaustion—dies, that is, from an excessive loss of the nutritive matters needed for its own activities.[53]

Once more, the deduction of materials for the propagation of the species may be postponed long enough to allow of great bulk and complex structure being attained. The procreative subtraction then setting in, while it checks and presently stops growth, may be so moderate as to leave vital capital sufficient to carry on the activities of the parent; may go on as long as parental vigour suffices to furnish, without fatal result, the materials needed to produce young ones; and may cease when such a surplus cannot be supplied, leaving the parental life to continue.

§ 326. The opposite side of this antagonism has also several aspects. Progress of organic evolution may be shown in increased bulk, in increased structure, in increased amount or variety of action, or in combinations of these; and under any of its forms this carrying higher of each individuality, implies a correlative retardation in the establishment of new individualities.

Other things equal, every normal addition to the bulk of an organism is an augmentation of its life.[54] Besides being an advance in integration, it implies a greater total of activities gone through in the assimilation of materials; and it implies, thereafter, a greater total of the vital changes taking place from moment to moment in all parts of the enlarged mass. Moreover, while increased size is thus, in so far, the expression of increased life, it is also, where the organism is active, the expression of increased ability to maintain life—increased strength. Aggregation of substance is almost the only mode in which self-preserving power is shown among the lowest types; and even among the highest, sustaining the body in its integrity is that in which self-preservation fundamentally consists—is the end which the widest intelligence is indirectly made to subserve. While, on the one hand, the increase of tissue constituting growth is conservative both in essence and in result; on the other hand, decrease of tissue, either from injury, disease, or old age, is in both essence and result the reverse. And if so, every addition to individual life thus implied, necessarily delays or diminishes the casting off of matter to form new individuals.

Other things equal, too, a greater degree of organization involves a smaller degree of that disorganization shown by the separation of reproductive gemmæ and germs. Detachment of a living portion or portions from what was previously a living whole, is a ceasing of co-ordination; and is therefore essentially at variance with that establishment of greater co-ordination which is achieved by structural development. In the extreme cases where a living mass is continually dividing and subdividing, it is manifest that there cannot arise much physiological division of labour; since progress towards mutual dependence of parts is prevented by the parts becoming independent. Contrariwise, it is equally clear that in proportion as the physiological division of labour is carried far, the separative process must be localized in some comparatively small portion of the organism, where it may go on without affecting the general structure—must become relatively subordinate. The advance that is shown by greater heterogeneity, must be a hindrance to multiplication in another way. For organization entails cost. That transfer and transformation of materials implied by differentiation, can be effected only by expenditure of force; and this supposes consumption of digested and absorbed food, which might otherwise have gone to make new organisms, or the germs of them. Hence, that individual evolution which consists in progressive differentiation, as well as that which consists in progressive integration, necessarily diminishes that species of dissolution, general or local, which propagation of the race exhibits.

In active organisms we have yet a further opposition between self-maintenance and maintenance of the race. All motion, sensible and insensible, generated by an animal for the preservation of its life, is motion liberated from decomposed nutriment—nutriment which, if not thus decomposed, would have been available for reproduction; or rather—might have been replaced by nutriment fitted for reproductive purposes, absorbed from other kinds of food. Hence, in proportion as the activities increase—in proportion as, by its more varied, complex, rapid, and vigorous actions, an animal gains power to support itself and to cope with surrounding dangers, it must lose power to propagate.

§ 327. How may this antagonism be best expressed in a brief way? If self-preservation displayed itself in the highest organisms, as it does in the lowest, in little else but continuous growth; and if race-preservation consisted always, as it does often, of nothing beyond detachment of portions from the parental mass; then the antagonism would be, throughout, the obviously-necessary one of integration and disintegration. Maintenance of the individual and propagation of the species, being respectively aggregative and separative, it would be as self-evident that they vary inversely, as it is self-evident that addition and subtraction undo one another. But though the simplest types show us the opposition of self-maintenance and race-maintenance almost wholly under this form; and though higher types, up to the most complex, exhibit it to a great extent under this form; yet, as we have just seen, this is not its only form. The total material monopolized by the individual and withheld from the race, must be stated as the quantity united to form its fabric, plus the quantity expended in differentiating its fabric, plus the quantity expended in its self-conserving actions. Similarly, the total material devoted to the race at the expense of the individual, includes that which is directly subtracted from the parent in the shape of egg or fœtus, plus that which is directly subtracted in the shape of milk, plus that which is indirectly subtracted in the shape of matter consumed in exertions for fostering the young. Hence this inverse variation is not expressible in simple terms of aggregation and separation. As we advance to more highly-evolved organisms, the total cost of an individual becomes very much greater than is implied by the amount of tissue composing it. So, too, the total cost of producing each new individual becomes very much greater than that of its mere substance. And it is between these two total costs that the antagonism exists.

We may, indeed, reduce the antagonism to a form comprehensive of all cases, if we consider it as existing between the sums of the forces, latent and active, used for the two purposes. The molecules which make up a plant or animal, have been formed by the absorption of forces directly or indirectly derived from the Sun; and hence the quantity of matter raised to the form called organic, which a plant or animal presents, is equivalent to a certain amount of force. Another amount of force is expressed by the totality of its differentiations. A further amount of force is that dissipated in its actions. And in these three amounts added together, we have the whole expense of the individual life. So, too, the whole expense of establishing each new individual includes—first the forces latent in the substance composing it when born or hatched; second the forces latent in the prepared nutriment afterwards supplied; and third the forces expended in feeding and protecting it. These two sets of forces being taken from a common fund, it is manifest that either set can increase only by decrease of the other. If, of the force which the parent obtains from the environment, much is consumed in its own life, little remains to be consumed in producing other lives; and, conversely, if there is a great consumption in producing other lives, it can only be where comparatively little is reserved for parental life.

Hence, then, Individuation and Genesis are necessarily antagonistic. Grouping under the word Individuation all processes by which individual life is completed and maintained; and enlarging the meaning of the word Genesis so as to include all processes aiding the formation and perfecting of new individuals; we see that the two are fundamentally opposed. Assuming other things to remain the same—assuming that environing conditions as to climate, food, enemies, &c., continue constant; then, inevitably, every higher degree of individual evolution is followed by a lower degree of race-multiplication, and vice versâ. Progress in bulk, complexity, or activity, involves retrogress in fertility; and progress in fertility involves retrogress in bulk, complexity, or activity.

This statement needs a slight qualification. For reasons to be hereafter assigned, the relation described is never completely maintained; and in the small departure from it, we shall find a remarkable self-acting tendency to further the supremacy of the most developed types. Here, however, this hint must suffice: explanation would carry us too far out of our line of argument. For the present it will not lead us astray if we regard this inverse variation of Individuation and Genesis as exact.

§ 328. Thus, then, the condition which each race must fulfil if it is to survive, is a condition which, in the nature of things, it ever tends to fulfil. In the last chapter we saw that a species cannot be maintained unless the power to preserve individual life and the power to propagate other individuals vary inversely. And here we have seen that, irrespective of an end to be subserved, these powers cannot do other than vary inversely. On the one hand, given a certain totality of destroying forces with which the species has to contend; and in proportion as its members have severally but small ability to resist these forces, it is requisite that they should have great ability to form new individuals, and vice versâ. On the other hand, given the quantity of force, absorbed as food or otherwise, which the species can use to counterbalance these destroying forces; and in proportion as much of it is expended in preserving the individual, little of it can be reserved for producing new individuals, and vice versâ. There is thus complete accordance between the requirements considered under each aspect. The two necessities correspond.

We might rest on these deductions and their several corollaries. Without going further we might with safety assert the general truths that, other things equal, advancing evolution must be accompanied by declining fertility; and that, in the highest types, fertility must still further decrease if evolution still further increases. We might be sure that if, other things equal, the relations between an organism and its environment become so changed as permanently to diminish the difficulties of self-preservation, there will be a permanent increase in the rate of multiplication; and, conversely, that a decrease of fertility will result where altered circumstances make self-preservation more laborious.

But we need not content ourselves with these à priori inferences. If they are true, there must be an agreement between them and the observed facts. Let us see how far such an agreement is traceable.