§ 74g. Here we come unawares to the remaining topic embraced under the title Cell-Life and Cell-Multiplication. We pass naturally from asexual multiplication of cells to sexual multiplication—from cell-reproduction to cell-generation. The phenomena are so numerous and so varied that a large part of them must be passed over. Conjugation among the Protophyta and Protozoa, beginning with cases in which there is a mingling of the contents of two cells in no visible respect different from one another, and developing into a great variety of processes in which they differ, must be left aside, and attention limited to the terminal process of fertilization as displayed in higher types of organisms.
Before fertilization there occurs in the ovum an incidental process of a strange kind—"strange" because it is a collateral change taking no part in subsequent changes. I refer to the production and extrusion of the "polar bodies." It is recognized that the formation of each is analogous to cell-formation in general; though process and product are both dwarfed. Apart from any ascribed meaning, the fact itself is clear. There is an abortive cell-formation. Abortiveness is seen firstly in the diminutive size of the separated body or cell, and secondly in the deficient number of its chromosomes: a corresponding deficiency being displayed in the group of chromosomes remaining in the egg—remaining, that is (on the hypothesis here to be suggested), in the sister-cell, supposing the polar body to be an aborted cell. It is currently assumed that the end to be achieved by thus extruding part of the chromosomes, is to reduce the remainder to half the number characterizing the species; so that when, to this group in the germ-cell, the sperm-cell brings a similarly-reduced group, union of the two shall bring the chromosomes to the normal number. I venture to suggest another interpretation. In doing this, however, I must forestall a conclusion contained in the next chapter; namely, the conclusion that gamogenesis begins when agamogenesis is being arrested by unfavourable conditions, and that the failing agamogenesis initiates the gamogenesis. Of numerous illustrations to be presently given I will, to make clear the conception, name only one—the formation of fructifying organs in plants at times when, and in places where, shoots are falling off in vigour and leaves in size. Here the successive foliar organs, decreasingly fitted alike in quality and dimensions for carrying on their normal lives, show us an approaching cessation of asexual multiplication, ending in the aborted individuals we call stamens; and the fact that sudden increase of nutrition while gamogenesis is being thus initiated, causes resumption of agamogenesis, shows that the gamogenesis is consequent upon the failing agamogenesis. See then the parallel. On going back from multicellular organisms to unicellular organisms (or those homologues of them which form the reproductive agents in multicellular organisms), we find the same law hold. The polar bodies are aborted cells, indicating that asexual multiplication can no longer go on, and that the conditions leading to sexual multiplication have arisen. If this be so, decrease in the chromatin becomes an initial cause of the change instead of an accompanying incident; and we need no longer assume that a quantity of precious matter is lost, not by passive incapacity, but by active expulsion. Another anomaly disappears. If from the germ-cell there takes place this extrusion of superfluous chromatin, the implication would seem to be that a parallel extrusion takes place from the sperm-cell. But this is not true. In the sperm-cell there occurs just that failure in the production of chromatin which, according to the hypothesis above sketched out, is to be expected; for, in the process of cell-multiplication, the cells which become spermatozoa are left with half the number of chromosomes possessed by preceding cells: there is actually that impoverishment and declining vigour here suggested as the antecedent of fertilization. It needs only to imagine the ovum and the polar body to be alike in size, to see the parallelism; and to see that obscuration of it arises from the accumulation of cytoplasm in the ovum.
A test fact remains. Sometimes the first polar body extruded undergoes fission while the second is being formed. This can have nothing to do with reducing the number of chromosomes in the ovum. Unquestionably, however, this change is included with the preceding changes in one transaction, effected by one influence. If, then, it is irrelevant to the decrease of chromosomes, so must the preceding changes be irrelevant: the hypothesis lapses. Contrariwise this fact supports the view suggested above. That extrusion of a polar body is a process of cell-fission is congruous with the fact that another fission occurs after extrusion. And that this occurs irregularly shows that the vital activities, seen in cell-growth and cell-multiplication, now succeed in producing further fission of the dwarfed cell and now fail: the energies causing asexual multiplication are exhausted and there arises the state which initiates sexual multiplication.
Maturation of the ovum having been completed, entrance of the spermatozoon, sometimes through the limiting membrane and sometimes through a micropyle or opening in it, takes place. This instantly initiates a series of complicated changes: not many seconds passing before there begins the formation of an aster around one end of the spermatozoon-head. The growth of this aster, apparently by linear rangings of the granules composing the reticulum of the germ-cell, progresses rapidly; while the whole structure hence arising moves inward. Soon there takes place the fusion of this sperm-nucleus with the germ-nucleus to form the cleavage-nucleus, which, after a pause, begins to divide and subdivide in the same manner as cells at large: so presently forming a cluster of cells out of which arise the layers originating the embyro. The details of this process do not concern us. It suffices to indicate thus briefly its general nature.
And now ending thus the account of genesis under its histological aspect, we pass to the account of genesis under its wider and more significant aspects.
CHAPTER VII.
GENESIS.
§ 75. Having, in the last chapter but one, concluded what constitutes an individual, and having, in the last chapter, contemplated the histological process which initiates a new individual, we are in a position to deal with the multiplication of individuals. For this, the title Genesis is here chosen as being the most comprehensive title—the least specialized in its meaning. By some biologists Generation has been used to signify one method of multiplication, and Reproduction to signify another method; and each of these words has been thus rendered in some degree unfit to signify multiplication in general.
Here the reader is indirectly introduced to the fact that the production of new organisms is carried on in fundamentally unlike ways. Up to quite recent times it was believed, even by naturalists, that all the various processes of multiplication observable in different kinds of organisms, have one essential character in common: it was supposed that in every species the successive generations are alike. It has now been proved, however, that in many plants and in numerous animals, the successive generations are not alike; that from one generation there proceeds another whose members differ more or less in structure from their parents; that these produce others like themselves, or like their parents, or like neither; but that eventually, the original form re-appears. Instead of there being, as in the cases most familiar to us, a constant recurrence of the same form, there is a cyclical recurrence of the same form. These two distinct processes of multiplication, may be aptly termed homogenesis and heterogenesis.[[28]] Under these heads let us consider them.
There are two kinds of homogenesis, the simplest of them, probably once universal but now exceptional, being that in which there is no other form of multiplication than one resulting from perpetual spontaneous fission. The rise of distinct sexes was doubtless a step in evolution, and before it took place the formation of new individuals could have arisen only by division of the old, either into two or into many. At present this process survives, so far as appears, among Bacteria, certain Algæ, and sundry Protozoa; though it is possible that a rarely-occurring conjugation has in these cases not yet been observed. It is a probable conclusion, however, that in the Bacteria at any rate, the once universal mode of multiplication still survives as an exceptional mode. But now passing over these cases, we have to note that the kind of genesis (once supposed to be the sole kind), in which the successive generations are alike, is sexual genesis, or, as it has been otherwise called—gamogenesis. In every species which multiplies by this kind of homogenesis, each generation consists of males and females; and from the fertilized germs they produce the next generation of similar males and females arises: the only needful qualification of this statement being that in many Protophyta and Protozoa the conjugating cells or protoplasts are not distinguishable in character. This mode of propagation has the further trait, that each fertilized germ usually gives rise to but one individual—the product of development is organized round one axis and not round several axes, Homogenesis in contrast with heterogenesis as exhibited in species which display distinct sexuality, has also the characteristic that each new individual begins as an egg detached from the maternal tissues, instead of being a portion of protoplasm continuous with them, and that its development proceeds independently. This development may be carried on either internally or externally; whence results the division into the oviparous and the viviparous. The oviparous kind is that in which the fertilized germ is extruded from the parent before it has undergone any considerable development. The viviparous kind is that in which development is considerably advanced, or almost completed, before extrusion takes place. This distinction is, however, not a sharply-defined one: there are transitions between the oviparous and the viviparous processes. In ovo-viviparous genesis there is an internal incubation; and though the young are in this case finally extruded from the parent in the shape of eggs, they do not leave the parent's body until after they have assumed something like the parental form. Looking around, we find that homogenesis is universal among the Vertebrata. Every vertebrate animal arises from a fertilized germ, and unites into its single individuality the whole product of this fertilized germ. In the mammals or highest Vertebrata, this homogenesis is in every case viviparous; in birds it is uniformly oviparous; and in reptiles and fishes it is always essentially oviparous, though there are cases of the kind above referred to, in which viviparity is simulated. Passing to the Invertebrata, we find oviparous homogenesis universal among the Arachnida (except the Scorpions, which are ovo-viviparous); universal among the higher Crustacea, but not among the lower; extremely general, though not universal, among Insects; and universal among the higher Mollusca though not among the lower. Along with extreme inferiority among animals, we find homogenesis to be the exception rather than the rule; and in the vegetal kingdom there appear to be no cases, except among the Algæ and a few aberrant parasites like the Rafflesiaceæ, in which the centre or axis which arises from a fertilized germ becomes the immediate producer of fertilized germs.