So long as the most eminent investigators (As for example the illustrious Wilhelm Hofmeister in his "Lehre von der Pflanzenzelle" (1867).) believed that the nucleus of a cell was destroyed in the course of each division and that the nuclei of the daughter-cells were produced de novo, theories of heredity were able to dispense with the nucleus. If they sought, as did Charles Darwin, who showed a correct grasp of the problem in the enunciation of his Pangenesis hypothesis, for histological connecting links, their hypotheses, or at least the best of them, had reference to the cell as a whole. It was known to Darwin that the cell multiplied by division and was derived from a similar pre-existing cell. Towards 1870 it was first demonstrated that cell-nuclei do not arise de novo, but are invariably the result of division of pre-existing nuclei. Better methods of investigation rendered possible a deeper insight into the phenomena accompanying cell and nuclear divisions and at the same time disclosed the existence of remarkable structures. The work of O. Butschli, O. Hertwig, W. Flemming H. Fol and of the author of this article (For further reference to literature, see my article on "Die Ontogenie der Zelle seit 1875", in the "Progressus Rei Botanicae", Vol. I. page 1, Jena, 1907.), have furnished conclusive evidence in favour of these facts. It was found that when the reticular framework of a nucleus prepares to divide, it separates into single segments. These then become thicker and denser, taking up with avidity certain stains, which are used as aids to investigation, and finally form longer or shorter, variously bent, rodlets of uniform thickness. In these organs which, on account of their special property of absorbing certain stains, were styled Chromosomes (By W. Waldeyer in 1888.), there may usually be recognised a separation into thicker and thinner discs; the former are often termed Chromomeres. (Discovered by W. Pfitzner in 1880.) In the course of division of the nucleus, the single rows of chromomeres in the chromosomes are doubled and this produces a band-like flattening and leads to the longitudinal splitting by which each chromosome is divided into two exactly equal halves. The nuclear membrane then disappears and fibrillar cell-plasma or cytoplasm invades the nuclear area. In animal cells these fibrillae in the cytoplasm centre on definite bodies (Their existence and their multiplication by fission were demonstrated by E. van Beneden and Th. Boveri in 1887.), which it is customary to speak of as Centrosomes. Radiating lines in the adjacent cell-plasma suggest that these bodies constitute centres of force. The cells of the higher plants do not possess such individualised centres; they have probably disappeared in the course of phylogenetic development: in spite of this, however, in the nuclear division-figures the fibrillae of the cell-plasma are seen to radiate from two opposite poles. In both animal and plant cells a