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136 Botanisches Centralblatt. — Beiheft 2. color, while the cytoplasm is of a brownish hue. The cytoplasm presents a regular fibrillar or alveolar arrangement. (Figs. 1 and 3.) The meshes especially in the younger cells are very small and their regularity in many cases is very striking. The cyto plasm , however, does not retain its homogeneous structure throughout the entire course of karyokinesis. B y the time the splindle is mature that portion of the cytoplasm immediately surrounding it has become very dense while the remaining cytoplasm reveals larger meshes and is less granular. In width this layer of protoplasm extends one half the distance across the cell (Figs. 3, 4, 5). Its margin is deeply wavy so that at places it approaches quite near the cell-wall. The remaining protoplasm of the cell has also changed for its meshes (Fig. 4) appear to be five or six times as large as they were in the earlier stages. The regularity of the protoplasmic meshes are now clearly less regular in outline. An examination of hundreds of specimens confirmed the above statements in every case. Development of the chromosomes. In the very early stages the nucleus, as above stated, pre sents a fine linin net. The threads of the net are at first smooth and uniform in diameter. In nuclei, however, which have ad vanced slightly beyond the resting stage the linin-net begins to show irregularities in width due to the appearance of larger granules. These granular masses constitute the chromatin. They are irregularly distributed in the linin net-work, and increasing in size ultimately form the chromosomes. A continuous chromatin It will be spirem does not seem to be developed in Magnolia. seen further that the nucleolus at this stage (Fig. 1) is very large staining densely and contains a conspicuous vacuole. The fibres of the linin network run to the nucleolus and are attached to it in such a way that a slight enlargement at the point of contact is visible. This was always found to be the case whether one or several nucleoli were present. These filiaments radiating from many points on its periphery seem to hold it in position. Its position was influenced in the direction of attachment of the greatest number of nuclear fibres (Fig. 1). At a later stage of karyokinesis (Fig. 2) we find that the nucleolus has entirely disapeared. It is probably utilized as food in the growth of the chromatin masses, for they stain much more readily and intensely at this time than at an earlier stage. The nuclear membrane which is now less distinct is gradually replaced by a weft of filaments closely interwoven. The threads of this weft are very fine, and the most careful staining is necessary to bring them out. The different forms which the chromosomes assume at this stage (Fig. 2) are due to a total or partial longitudinal splitting and a subsequent bending. This longitudinal cleavage is recognized as a rather clear line which appears through the length of the chromosome (Fig. 2). After this division the chromosomes bend