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Hertwig in 1875.) and this afforded a new support for the correct conception of the nuclear functions. The minute study of the behaviour of the other constituents of sexual cells during fertilisation led to the result, that the nucleus alone is concerned with handing on hereditary characters (This was done by O. Hertwig and the author of this essay simultaneously in 1884.) from one generation to another. Especially important, from the point of view of this conclusion, is the study of fertilisation in Angiosperms (Flowering plants); in these plants the male sexual cells lose their cell-body in the pollen-tube and the nucleus only--the sperm-nucleus--reaches the egg. The cytoplasm of the male sexual cell is therefore not necessary to ensure a transference of hereditary characters from parents to offspring. I lay stress on the case of the Angiosperms because researches recently repeated with the help of the latest methods failed to obtain different results. As regards the descendants of angiospermous plants, the same laws of heredity hold good as for other sexually differentiated organisms; we may, therefore, extend to the latter what the Angiosperms so clearly teach us.

The next advance in the hitherto rapid progress in our knowledge of nuclear division was delayed, because it was not at once recognised that there are two absolutely different methods of nuclear division. All such nuclear divisions were united under the head of indirect or mitotic divisions;these were also spoken of as karyo-kineses, and were distinguished from the direct or amitotic divisions which are characterised by a simple constriction of the nuclear body. So long as the two kinds of indirect nuclear division were not clearly distinguished, their correct interpretation was impossible. This was accomplished after long and laborious research, which has recently been carried out and with results which should, perhaps, be regarded as provisional.

Soon after the new study of the nucleus began, investigators were struck by the fact that the course of nuclear division in the mother-cells, or more correctly in the grandmother-cells, of spores, pollen-grains, and embryo-sacs of the more highly organised plants and in the spermatozoids and eggs of the higher animals, exhibits similar phenomena, distinct from those which occur in the somatic cells.

In the nuclei of all those cells which we may group together as gonotokonts (At the suggestion of J.P. Lotsy in 1904.) (i.e. cells concerned in reproduction) there are fewer chromosomes than in the adjacent body-cells (somatic cells). It was noticed also that there is a peculiarity characteristic of the gonotokonts, namely the occurrence of two nuclear divisions rapidly succeeding one another. It was afterwards recognised that in the first stage of nuclear division in the gonotokonts the chromosomes unite in pairs: it is these chromosome-pairs, and not the two longitudinal halves of single chromosomes, which form the nuclear plate in the equatorial plane of the nuclear spindle. It has been proposed to call these pairs gemini. (J.E.S. Moore and A.L. Embleton, "Proc. Roy. Soc."London, Vol. LXXVII. page 555, 1906; V. Gregoire, 1907.) In the course of this division the spindle-fibrillae attach themselves to the gemini, i.e. to entire chromosomes and direct them to the points where the new daughter-nuclei are formed, that is to those positions towards which the longitudinal halves of the chromosomes travel in ordinary nuclear divisions. It is clear that in this way the number of chromosomes which the daughter-nuclei contain, as the result of the first stage in division in the gonotokonts, will be reduced by one half, while in ordinary divisions the number of chromosomes always remains the same. The first stage in the division of the nucleus in the gonotokonts has therefore been termed the reduction division. (In 1887 W. Flemming termed this the heterotypic form of nuclear division.) This stage in division determines the conditions for the second division which rapidly ensues. Each of the paired chromosomes of the mother-nucleus has already, as in an ordinary nuclear division, completed the longitudinal fission, but in this case it is not succeeded by the immediate separation of the longitudinal halves and their allotment to different nuclei. Each chromosome, therefore, takes its two longitudinal halves into the same daughter-nucleus. Thus, in each daughter-nucleus the longitudinal halves of the chromosomes are present ready for the next stage in the division; they only require to be arranged in the nuclear plate and then distributed among the granddaughter-nuclei.

This method of division, which takes place with chromosomes already split, and which have only to provide for the distribution of their longitudinal halves to the next nuclear generation, has been called homotypic nuclear division. (The name was proposed by W. Flemming in 1887; the nature of this type of division was, however, not explained until later.)Reduction division and homotypic nuclear division are included together under the term allotypic nuclear division and are distinguished from the ordinary or typical nuclear division. The name Meiosis (By J. Bretland Farmer and J.E.S. Moore in 1905.) has also been proposed for these two allotypic nuclear divisions. The typical divisions are often spoken of as somatic.