By A. L. Yudin (auth.), T. A. Dettlaff, S. G. Vassetzky (eds.)
This quantity contains common tables (description of ordinary improvement) for protozoa and invertebrates wide-spread in developmental biology experiences. The species selected mirror their merits for laboratory reports, the knowledge avail capable, and their availability for experimentation. bankruptcy eleven, which incorporates the traditional tables for the starfish Asterina pectinifera, used to be written especially for this edi tion, that is the invertebrate part of the revised and augmented translation of Ob"ekty Biologii Razvitiya released in Russian in 1975 as a quantity within the sequence of monographs Problemy Biologii Razyitiya (Problems of Developmental Biology) via Nauka Publishers, Moscow. the outline of each species is preceded through an creation within which the benefits of operating with the actual animal are said and the issues stud ied (with the most references) are defined. info also are supplied on its taxonomic prestige and distribution of the animal, and stipulations of retaining the grownup animals in laboratory. equipment of acquiring gametes, tools of man-made fertilization, meth ods of rearing embryos and larvae, and tables of ordinary improvement also are given.
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Additional resources for Animal Species for Developmental Studies: Volume 1 Invertebrates
The stock solution of trace elements should be prepared at least two weeks before use, and the solution may then be kept for more than one year. 1 50 grams of N a2EDTA is then dissolved in 250 ml water by heating. The first solution is heated to 100°C, mixed with the EDTA solution, and brought to the boil. 8 by titration at 70-90°C adding no more than 100 ml of 20% KOH solution. The pH-meter should be calibrated using a standard buffer at 75°C. The volume is adjusted to 1 liter. After 2 weeks of storage in a loosely corked flask the green solution turns purple.
Pilner, "Adenosine-3',5'-cyclic monophosphate in Chlamydomonas reinhardii: influence on flagellar function and regeneration," J. Cell Bioi. 56, 628-635 (1973). 57. R. S. Ryan, D. Grant, Chiang Kwen-Sheng, and H. Swift, "Isolation of mitochondria and characterization of the mitochondrial DNA of Chlamy. domonas reinhardii," J. Cell Bioi. 59, Pt. 2, 297a (1973a). 58. R. Sager, "Mendelian and non-Mendelian inheritance of streptomycin resistance in Chlamydomonas," Proc. Natl. Acad. Sci. USA 40,356-370 (1954).
31. 31-37 (1973). 64. F. SchOtz, H. Bathelt, C. G. Arnold, and O. Schimmer, "Die Architectur und Organization der Chlamydomonas-celIe. Ergebnisse der Elektronenmikroskopie von Serienschnitten und der daraus resultierenden dreidimensionalen Reconstruktion," Protoplasma 75,229-254 (1972). 65. D. Starling, "Complementation tests in closely'linked flagellar genes in Chlamydomonas reinhardii, Genet. Res. 14,343-347 (1969). 66. R. C. Starr, "Algae cultures - sources and methods of cultivation," in: Methods in Enzymology, Vol.