The investigations of microscopists indicate that it does—that evolution has provided it with these favorable circumstances, in the bodies of the higher animals. Let us recall in outline the early history of the fertilized germ-cell, the zygote formed by the union of ovum and spermatozoön. These two unite to form a single cell, which is essentially the same, physiologically, as other germ-cells. It divides in two similar cells; these each divide; the resulting cells again divide, and so the process continues, until the whole body—a fully developed man,—has been produced by division and redivision of the one zygote.
But the germ-cell is obviously different from most of the cells that make up the finished product, the body. The latter are highly differentiated and specialized for different functions—blood cells, nerve cells, bone cells, muscle cells, and so on, each a single cell but each adapted to do a certain work, for which the original, undifferentiated germ-cell was wholly unfit. It is evident that differentiation began to take place at some point in the series of divisions, that is to say, in the development of the embryo.
Th. Boveri, studying the development of a threadworm, made the interesting discovery that this differentiation began at the first division. Of the two daughter-cells produced from the zygote, one continued dividing at a very slow rate, and without showing any specialization. Its "line of descent" produced only germ-cells. The products of division of the other daughter-cell began to differentiate, and soon formed all the necessary kinds of cells to make up the body of the mature worm. In this body, the cells from the first daughter-cell mentioned were inclosed, still undifferentiated: they formed the germ-cells of the next generation, and after maturity were ready to be ejected from the body, and to form new threadworms.
Imagine this process taking place through generation after generation of threadworms, and one will realize that the germ-plasm was passed on directly from one generation to the next; that in each generation it gave rise to body-plasm, but that it did not at any time lose its identity or continuity, a part of the germ-plasm being always set aside, undifferentiated, to be handed on to the next generation.
In the light of this example, one can better understand the definition of germ-plasm as "that part of the substance of the parents which does not die with them, but perpetuates itself in their offspring." By bringing his imagination into play, the reader will realize that there is no limit to the backward continuity of this germ-plasm in the threadworm. Granted that each species has arisen by evolution from some other, this germ-cell which is observed in the body of the threadworm, must be regarded as part of what may well be called a stream of germ-plasm, that reaches back to the beginning of life in the world. It will be equally evident that these is no foreordained limit to the forward extension of the stream. It will continue in some branch, as long as there are any threadworms or descendants of threadworms in the world.
The reader may well express doubt as to whether what has been demonstrated for the threadworm can be demonstrated for the higher animals, including man. It must be admitted that in many of these animals conditions are too unfavorable, and the process of embryology too complicated, or too difficult to observe, to permit as distinct a demonstration of this continuity of the germ-plasm, wherever it is sought. But it has been demonstrated in a great many animals; no facts which impair the theory have been discovered; and biologists therefore feel perfectly justified in generalizing and declaring the continuity of germ-plasm to be a law of the world of living things.
Focusing attention on its application to man, one sees that the race must represent an immense network of lines of descent, running back through a vast number of different forms of gradually diminishing specialization, until it comes to a point where all its threads merge in one knot—the single cell with which it may be supposed that life on this globe began. Each individual is not only figuratively, but in a very literal sense, the carrier of the heritage of the whole race—of the whole past, indeed. Each individual is temporarily the custodian of part of the "stuff of life"; from an evolutionary point of view, he may be said to have been brought into existence, primarily to pass this sacred heritage on to the next generation. From Nature's standpoint, he is of little use in the world, his existence is scarcely justified, unless he faithfully discharges this trust, passing on to the future the "Lamp of Life" whose fire he has been created to guard for a short while.
Immortality, we may point out in passing, is thus no mere hope to the parent: it is a real possibility. The death of the huge agglomeration of highly specialized body-cells is a matter of little consequence, if the germ-plasm, with its power to reproduce not only these body-cells, but the mental traits—indeed, we may in a sense say the very soul—that inhabited them, has been passed on. The individual continues to live, in his offspring, just as the past lives in him. To the eugenist, life everlasting is something more than a figure of speech or a theological concept—it is as much a reality as the beat of the heart, the growth of muscles or the activity of the mind.
This doctrine of the continuity of germ-plasm throws a fresh light on the nature of human relationships. It is evident that the son who resembles his father can not accurately be called a "chip off the old block." Rather, they are both chips off the same block; and aside from bringing about the fusion of two distinct strains of germ-plasm, father and mother are no more responsible for endowing the child with its characters except in the choice of mate, than is the child for "stamping his impress" on his parents. From another point of view, it has been said that father and son ought to be thought of as half-brothers by two different mothers, each being the product of the same strain of paternal germ-plasm, but not of the same strain of maternal germ-plasm. Biologically, the father or mother should not be thought of as the producer of a child, but as the trustee of a stream of germ-plasm which produces a child whenever the proper conditions arise. Or as Sir Michael Foster put it, "The animal body is in reality a vehicle for ova or sperm; and after the life of the parent has become potentially renewed in the offspring, the body remains as a cast-off envelope whose future is but to die." Finally to quote the metaphor of J. Arthur Thomson, one may "think for a moment of a baker who has a very precious kind of leaven; he uses much of this in baking a large loaf; but he so arranges matters by a clever contrivance that part of the original leaven is always carried on unaltered, carefully preserved for the next baking. Nature is the baker, the loaf is the body, the leaven is the germ-plasm, and each baking is a generation."
When the respective functions and relative importance, from a genetic point of view, of germ-plasm and body-plasm are understood, it must be fairly evident that the natural point of attack for any attempt at race betterment which aims to be fundamental rather than wholly superficial, must be the germ-plasm rather than the body-plasm. The failure to hold this point of view has been responsible for the disappointing results of much of the sociological theory of the last century, and for the fact that some of the work now carried on under the name of race betterment is producing results that are of little or no significance to true race betterment.