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 specialization of the nuclear changes in the process of maturation and fertilization of the generative cells, there is more than sufficient reason for believing that the nuclear substance, if not actually the specific germ-plasm, is of vast importance in heredity. The theory of its absolute dominance depends on a number of experiments, the interpretation of which is doubtful. Moritz Nussbaum showed that in Infusoria non-nucleated fragments of a cell always died, while nucleated fragments were able to complete themselves; but it may be said with almost equal confidence that nuclei separated from protoplasm also invariably die—at least, all attempts to preserve them have failed. Hertwig and others, in their brilliant work on the nature of fertilization, showed that the process always involved the entrance into the female cell of the nucleus of the male cell, but we now know that part of the protoplasm of the spermatozoon also enters. T. Boveri made experiments on the cross-fertilization of non-nucleated fragments of the eggs of Sphaerechinus granularis with spermatozoa of Echinus microtuberculatus, and obtained dwarf larvae with only the paternal characters; but the nature of his experiments was not such as absolutely to exclude doubt. Finally, in addition to the nucleus and the protoplasm, another organism of the cell, the centrosome, is part of the hereditary mass. In sum, while most of the evidence points to a preponderating importance of the nuclear matter, it cannot be said to be an established proposition that the nuclear matter is the germ-plasm. Nor are we yet definitely in a position to say that the germinal mass (nuclear matter, protoplasm, &c., of the reproductive cells) differs essentially from the general substance of the organism—whether, in fact, there is continuity of germ-plasm as opposed to continuity of living material from individual to individual. The origin of sexual cells from only definite places, in the vast majority of cases, and such phenomena as the phylo-genetic migration of their place of origin among the Hydro-medusae, tell strongly in favour of Weismann’s conception. Early experiments on dividing eggs, in which, by separation or transposition, cells were made to give rise to tissues and parts of the organism which in the natural order they would not have produced, tell strongly against any profound separation between germ-plasm and body-plasm. It is also to be noticed that the failure of germ-cells to arise except in specific places may be only part of the specialized ordering of the whole body, and does not necessarily involve the interpretation that reproductive material is absolutely different in kind.

Amphimixis.—Hitherto we have considered the material bearer of heredity apart from the question of sexual union, and we find that the new organism takes origin from a portion of living matter, forming a material which may be called germ-plasm, in which resides the capacity to correspond to the same kind of surrounding forces as stimulated the parent germ-plasm by growth of the same fashion. In many cases (e.g. asexual spores) the piece of germ-plasm comes from one parent, and from an organ or tissue not associated with sexual reproduction; in other cases (parthenogenetic eggs) it comes from the ovary of a female, and may have the apparent characters of a sexual egg, except that it develops without fertilization; here also are to be included the cases where normal female ova have been induced to develop, not by the entrance of a spermatozoon, but by artificial chemical stimulation. In such cases the problem of heredity does not differ fundamentally from the symmetrical repetition of parts. In most of the higher plants and animals, however, sexual reproduction is the normal process, and from our present point of view the essential feature of this is that the germ-plasm which starts the new individual (the fertilized egg) is derived from the male (the spermatozoon) and from the female parent (the ovum). Although it cannot yet be set down sharply as a general proposition, there is considerable evidence to show that in the preparation of the ovum and spermatozoon for fertilization the nuclear matter of each is reduced by half (reducing division of the chromosomes), and that fertilization means the restoration of the normal bulk in the fertilized cell by equal contributions from male and female. So far as the known facts of this process of union of germ-plasms go, they take us no farther than to establish such a relation between the offspring and two parents as exists between the offspring and one parent in the other cases. Amphimixis has a vast importance in the theory of evolution (Weismann, for instance, regards it as the chief factor in the production of variations); for its relation to heredity we are as yet dependent on empirical observations.

Heredity and Development.—The actual process by which the germinal mass slowly assumes the characters of the adult—that is, becomes like the parent—depends on the interaction of two sets of factors: the properties of the germinal material itself, and the influences of substances and conditions external to the germinal material. Naturally, as K. W. von Nägeli and Hertwig in particular have pointed out, there is no perpetual sharp contrast between the two sets of factors, for, as growth proceeds, the external is constantly becoming the internal; the results of influences, which were in one stage part of the environment, are in the next and subsequent stages part of the embryo. The differences between the exponents of evolution and epigenesis offer practical problems to be decided by experiment. Every phenomenon in development that is proved the direct result of epigenetic factors can be discounted from the complexity of the germinal mass. If, for instance, as H. Driesch and Hertwig have argued, much of the differentiation of cells and tissues is a function of locality and is due to the action of different external forces on similar material, then just so much burden is removed from what evolutionists have to explain. That much remains cannot be doubted. Two eggs similar in appearance develop side by side in the same sea-water, one becoming a mollusc, the other an Amphioxus. Hertwig would say that the slight differences in the original eggs would determine slight differences in metabolism and so forth, with the result that the segmentation of the two is slightly different; in the next stage the differences in metabolisms and other relations will be increased, and so on indefinitely. But in such cases c’est le premier pas qui coûte, and the absolute cost in theoretical complexity of the germinal material can be estimated only after a prolonged course of experimental work in a field which is as yet hardly touched.

Empirical Study of Heredity.—The fundamental basis of heredity is the separation of a mass from the parent (germ-plasm) which under certain conditions grows into an individual resembling the parent. The goal of the study of heredity will be reached only when all the phenomena can be referred to the nature of the germ-plasm and of its relations to the conditions under which it grows, but we have seen how far our knowledge is from any attempt at such references. In the meantime, the empirical facts, the actual relations of the characters in the offspring to the characters of the parents and ancestors, are being collected and grouped. In this inquiry it at once becomes obvious that every character found in a parent may or may not be present in the offspring. When any character occurs in both, it is generally spoken of as transmissible and of having been transmitted. In this broad sense there is no character that is not transmissible. In all kinds of reproduction, the characters of the class, family, genus, species, variety or race, and of the actual individual, are transmissible, the certainty with which any character appears being almost in direct proportion to its rank in the descending scale from order to individual. The transmitted characters are anatomical, down to the most minute detail; physiological, including such phenomena as diatheses, timbre of voice and even compound phenomena, such as gaucherie and peculiarity of handwriting; psychological; pathological; teratological, such as syndactylism and all kinds of individual variations. Either sex may transmit characters which in themselves are necessarily latent, as, for instance, a bull may transmit a good milking strain. In forms of asexual reproduction, such as division, budding, propagation by slips and so forth, every character of the parent may appear in the descendant, and apparently even in the descendants produced from that descendant by the ordinary sexual processes. In reproduction by spore formation, in parthenogenesis and in ordinary sexual modes, where there is an embryological history between the separated mass and the new adult, it is necessary