THE REACTIONS OF CERIANTHUS TO LIGHT

1. When Cerianthus membranaceus is illuminated upon one side, the animal turns its anterior portion toward the source of light. The number of degrees through which the animal turns is proportional to the logarithm of the intensity of the light. 2. A light intensity of between 250 m.c. and 15,000 m.c. is necessary to cause retraction of the animal. 3. The part of the spectrum which is most effective in causing heliotropic bending of Cerianthus lies between µµ 510 and µµ 570.     

LOCAL AND SYSTEMIC CONTROL OF GRANULOCYTIC AND MACROPHAGE PROGENITOR CELL REGENERATION AFTER IRRADIATION

Agar cultures of C₅₇BL bone marrow cells were used to determine colony stimulating factor (CSF) and serum CSF-inhibitor levels in C₅₇BL and BALB/c mice following irradiation. Whole-body irradiation caused an acute, dose-dependent, rise in serum CSF levels and fall in CSF-inhibitor levels. The regeneration of granulocytic and macrophage progenitor cells ( in vitro CFCs) in the femur after 250 rads whole-body irradiation was preceded or paralleled by a fall in serum CSF-inhibitors and a dramatic rise in the capacity of bone-adherent cells in the marrow ('stromal cells') to produce material with colony-stimulating activity. No comparable changes were observed in the activity of marrow haemopoietic cells during regeneration or in the lungs or spleen. A similar rise in the activity of bone-adherent cells was observed in shielded femurs during regeneration of in vitro CFCs.
Regeneration of granulocytic and macrophage progenitor cells following irradiation may be regulated by fluctuations in circulating CSF-inhibitor levels and local production of CSF within the marrow cavity.     

Bud Induction with Cytokinin : A LOCAL RESPONSE TO LOCAL APPLICATION

A portion of the surface of detached Graptopetalum paraquayense E. Walther leaves can be used to assay small amounts of reagents in lanolin for their ability to induce shoots only at the site of application. The cytokinins benzyladenine, kinetin, and 6-(γ,γ-dimethylallylamino)purine (DMAAP) were tested, and DMAAP was most effective in bud induction at concentrations below 1%. The higher the hormone concentration, the sooner the appearance of leaf primordia and the higher the ultimate yield of buds. Leaves treated with DMAAP for 2 days developed buds as rapidly as those with longer treatments.     

我国地方植物志出版情况简介

<正> 近年来,我国植物志的编写、出版工作较为喜人。除了世界瞩目的《中国植物志》(共80卷125分册,目前已出版50多卷册)外,地方植物志的编写、出版也取得了较大进展。为使读者能有一个较系统地了解,笔者根据北京图书馆、中国科学院图书馆、中国科学院植物研究所图书馆及北京师范大学生物系资料室所收藏的资料作了如下统计,出版时间截止1988年底。因依据的资料有限,一定还有遗漏,欢迎海内外学者指正。另外本文范围仅限高等植物。     

REACTIONS OF VALONIA AND OF HALICYSTIS TO COLLOIDS

From the results of these tests it is clear that both Halicystis and Valonia have a high degree of tolerance for animal peptone, and a very high degree of tolerance for animal proteose and for egg albumen. The products of bacterial growths fostered by these proteins have a deleterious effect upon both species of algae; but, if it were possible to prevent bacterial growth entirely and at the same time supply proper food, it is probable that Halicystis and Valonia would show normal growth indefinitely in the presence of these three colloids. This is not true where exposure is made to yeast nucleic acid dissolved in sea water containing 0.00093 gm. per cc. of NaOH. Valonia is markedly less tolerant of this medium (perhaps of NaOH rather than the colloid used) than Halicystis. Such differential effects, however, reach a high point in the case of the solutions of diphtheria toxin and of edestin. Halicystis has a very high tolerance for diphtheria toxin, and Valonia a very low tolerance. In the case of edestin, the relationship is reversed. Here Halicystis has a very low tolerance, and Valonia a very high tolerance. In fact, it may be said that diphtheria toxin has no appreciable effect upon Halicystis, and edestin a very slight effect upon Valonia; while diphtheria toxin is extremely toxic to Valonia, and edestin is extremely toxic to Halicystis. We can offer no suggestions, at present, as to the way in which these effects are produced. It is probable that the very thin protoplasmic layer of these species, which is certainly no thicker than 8µ, is sufficient to obstruct the passage of proteins having large molecules, like egg albumen, with a degree of efficiency that is extraordinary. In the tests we have reported, areas of from 20 sq. cm. to 40 sq. cm. have been submitted to the action of a relatively high concentration of egg albumen for several days without permitting the passage of sufficient amounts to give definable tests either with Spiegler''s or with Tanret''s method,— presumably less than 1 part in 250,000. In the tests of the proteins having much smaller molecules (though the size may not be the explanation), there is some probability that the membranes exhibit a little permeability. The peptone and the proteose of animal origin, or biuret-positive substances derived from them, apparently pass the protoplasmic membranes occasionally in quantities sufficient to give biuret tests. The most probable case of protein passage, however, was that of the proteose of the scarlet runner bean, where specific detection of less than 1 part per 80,000 was possible. In this instance the proteose appeared to pass membranes that were healthy and were functioning normally. But since the cells of the algae had to be destroyed in making the tests, one cannot maintain this point. All one can say is that protein passage was indicated in carefully examined cells of both species, where no breaks in the protoplasmic membrane were discernible, and where samples of the treated cells behaved normally after treatment.