In the stages preliminary to their division, the chromosomes become denser and take up a substance which increases their staining capacity; this is called chromatin. This substance collects in the chromomeres and may form the nutritive material for the carriers of hereditary units which we now believe to be enclosed in them. The chromatin cannot itself be the hereditary substance, as it afterwards leaves the chromosomes, and the amount of it is subject to considerable variation in the nucleus, according to its stage of development. Conjointly with the materials which take part in the formation of the nuclear spindle and other processes in the cell, the chromatin accumulates in the resting nucleus to form the nucleoli.
Naturally connected with the conclusion that the nuclei are the carriers of hereditary characters in the organism, is the question whether enucleate organisms can also exist. Phylogenetic considerations give an affirmative answer to this question. The differentiation into nucleus and cytopla** represents a division of labour in the protoplast. A study of organisms which belong to the lowest class of the organic world teaches us how this was accomplished. Instead of well-defined nuclei, scattered granules have been described in the protoplasm of several of these organisms (Bacteria, Cyanophyceae, Protozoa.), characterised by the same reactions as nuclear material, provided also with a nuclear network, but without a limiting membrane. (This is the result of the work of R. Hertwig and of the most recently published investigations.) Thus the carriers of hereditary characters may originally have been distributed in the common protoplasm, afterwards coming together and eventually assuming a definite form as special organs of the cell. It may be also assumed that in the protoplasm and in the primitive types of nucleus, the carriers of the same hereditary unit were represented in considerable quantity; they became gradually differentiated to an extent commensurate with newly acquired characters.
It was also necessary that, in proportion as this happened, the mechanism of nuclear division must be refined. At first processes resembling a ****** constriction would suffice to provide for the distribution of all hereditary units to each of the products of division, but eventually in both organic kingdoms nuclear division, which alone insured the qualitative identity of the products of division, became a more marked feature in the course of cell-multiplication.
Where direct nuclear division occurs by constriction in the higher organisms, it does not result in the halving of hereditary units. So far as my observations go, direct nuclear division occurs in the more highly organised plants only in cells which have lost their specific functions.
Such cells are no longer capable of specific reproduction. An interesting case in this connection is afforded by the internodal cells of the Characeae, which possess only vegetative functions. These cells grow vigorously and their cytopla** increases, their growth being accompanied by a correspondingly direct multiplication of the nuclei. They serve chiefly to nourish the plant, but, unlike the other cells, they are incapable of producing any offspring. This is a very instructive case, because it clearly shows that the nuclei are not only carriers of hereditary characters, but that they also play a definite part in the metabolism of the protoplasts.
Attention was drawn to the fact that during the reducing division of nuclei which contain chromosomes of unequal size, gemini are constantly produced by the pairing of chromosomes of the same size. This led to the conclusion that the pairing chromosomes are homologous, and that one comes from the father, the other from the mother. (First stated by T.H. Montgomery in 1901 and by W.S. Sutton in 1902.) This evidently applies also to the pairing of chromosomes in those reduction-divisions in which differences in size do not enable us to distinguish the individual chromosomes. In this case also each pair would be formed by two homologous chromosomes, the one of paternal, the other of maternal origin. When the separation of these chromosomes and their distribution to both daughter-nuclei occur a chromosome of each kind is provided for each of these nuclei. It would seem that the components of each pair might pass to either pole of the nuclear spindle, so that the paternal and maternal chromosomes would be distributed in varying proportion between the daughter-nuclei; and it is not impossible that one daughter-nucleus might occasionally contain paternal chromosomes only and its sister-nucleus exclusively maternal chromosomes.