锦鸡儿属植物4个种的核型分析

对4种锦鸡儿属(CaraganaFabr.)植物的核型进行了分析,得出4种染色体核型:秦晋锦鸡儿(C.purdom iiRehd.)染色体数为2n=16,其核型公式为2n=16=16 m(4 SAT);小叶锦鸡儿(C.m icrophyllaLam.)染色体数为2n=16,其核型公式为2n=16=14 m(2 SAT) 2 M;中间锦鸡儿(C.interm ediaKuang et H.C.Fu)染色体数为2n=18,其核型公式为2n=18=16 m(4 SAT) 2 M;树锦鸡儿(C.arborescensLam.)染色体数为2n=20,其核型公式为2n=20=20 m(4 SAT)。由此可推测:中间锦鸡儿可能为小叶锦鸡儿和树锦鸡儿或秦晋锦鸡儿和树锦鸡儿的中间类型或杂交种,也可能是具有递增染色体基数的不同种。     

角堇与大花三色堇染色体核型分析

以2份角堇与4份大花三色堇自交系为试验材料,采用染色体常规压片方法,观察和分析了它们的细胞染色体数目、相对长度、平均臂比等核型指标,以明确两种植物细胞学特点,为分类以及育种提供理论依据。结果表明:(1)2份角堇自交系染色体数目均为2n=2x=26,染色体基数为x=13,染色体核型公式分别为2n=2x=26=8m+12sm+6st、2n=2x=26=4m+16sm+6st,核型不对称系数为67.20%~70.10%,核型分类均属于3B。(2)4份大花三色堇自交系均为四倍体,其中2份(EYO-1-2-1-4、DSRFY-1-1-2)染色体数目为44,核型公式为2n=4x=44=4m+16sm+6st、2n=4x=44=16m+24sm+4st;2份(G10-1-3-1-4、XXL-YB-1-1-1-1)染色体数目为48,核型公式分别为2n=4x=48=8m+20sm+20st、2n=4x=48=4m+36sm+8st,核型不对称系数为66.74%~71.77%,核型分类属于2B、3B。     

黄芪属六种植物的核型多样性

采用常规压片法,对豆科黄芪属6种植物制备染色体标本进行核型分析。结果表明:体细胞中期染色体数目分别为:沙打旺、斜茎黄芪、达乌里黄芪2n=16,均为二倍体;草木樨状黄芪2n=32,为四倍体;紫云英、鹰嘴紫云英则呈现多数目性,紫云英染色体数变动范围为55～65,64条稍多,鹰嘴紫云英染色体数变动范围51～65,62条稍多,均为混倍体。核型公式分别为:沙打旺2n=2x=16=12m+4sm;斜茎黄芪2n=2x=16=10m+6sm;达乌里黄芪2n=2x=16=16m;草木樨状黄芪2n=4x=32=32m;紫云英2n=64=62m+2sm;鹰嘴紫云英2n=62=12M+50m(2SAT)。染色体核型呈现多样性。     

中国淡水三角涡虫(Dugesia sp)的染色体研究(Ⅰ)

利用空气干燥法对不同产地淡水三角涡虫的染色体进行了研究。核型分析表明：河南淇县鱼泉三角涡虫(Dugesia sp)和浙江杭州龙井三角涡虫(Dugesia sp)体细胞中有16条染色体,为二倍体,核型公式为2n=2x=16=16m,均为具中部着丝粒染色体;河南济源不老泉三角涡虫(Dugesia sp)有24条染色体,为三倍体,核型公式为2n=3x=24=24m,亦全部由中部着丝粒染色体组成。上述3个产地淡水三角涡虫染色体的形态较为接近。北京樱桃沟三角涡虫(Dugesia sp)的体细胞染色体数目为24,为三倍体,核型公式为2n=3x=24=22m 2sm,由中部和亚中部着丝粒染色体组成,其中第2、4号各有一条染色体属于亚中部着丝粒染色体。研究结果表明：4个产地三角涡虫的体细胞染色体数目存在较大差异,包括二倍体(2n=2x=16)和三倍体(2n=3x=24),染色体基数属于x=8类型。     

锦鸡儿属3种植物的核型研究

以锦鸡儿属中间锦鸡儿、柠条锦鸡儿、狭叶锦鸡儿为材料,用光学显微镜观察了3种锦鸡儿的染色体,按全国第一次植物染色体学术讨论会建议的标准进行了核型分析。结果表明,3种锦鸡儿的体细胞染色体数目2n=16,核型公式分别为:中间锦鸡儿2n=2x=16=10m 6sm、柠条锦鸡儿2n=2x=16=12m 4sm、狭叶锦鸡儿2n=2x=16=14m 2sm,中间锦鸡儿和柠条锦鸡儿的核型属于2A型,狭叶锦鸡儿的核型属于2B型。狭叶锦鸡儿二倍体染色体核型为首次报道。     

不同地域乌拉尔甘草基因组的FISH分析与染色体识别

在核型分析与染色体识别基础上,分别以番茄45S和5S rDNA为探针,对3种不同地域的乌拉尔甘草进行FISH分析.结果表明:内蒙古鄂托克前旗的乌拉尔甘草核型公式为2n=2x=16=6m+10sm (2SAT),新疆阿勒泰地区的乌拉尔甘草核型公式为2n=2x=16=4m+12sm(2SAT),内蒙古喀喇沁旗乌拉尔甘草核型公式为2n=2x=16=4m+12sm(2SAT);其第8染色体均带有随体.3种乌拉尔甘草基因组内均有1对5S rDNA和1对45S rDNA杂交位点.核型分析显示,5S rDNA杂交位点均位于第2染色体的短臂部位,45S rDNA杂交位点均位于第8染色体的次缢痕和随体部位.45S与5S rDNA在3种乌拉尔甘草中期分裂相上的位点数和分布情况高度一致,表明来自3种不同地域的乌拉尔甘草在染色体结构水平上没有较大的分化.     

二倍体铁破锣的核型及四倍体细胞型的首次发现

本文重新检查了铁破锣的核型。来自湖南新宁的40个个体中,1个个体为四倍体,其核型公式为2n＝4x=32=16m+8sm+4st+4t;其余个体为二倍体,其核型公式为2n＝2x＝16=8m+4sm+2st+2t。来自云南大理的10个个体全为四倍体,其核型公式为2n=4x=32＝16m+8sm+4st+4t。据此认为商效民(1985)报道的该种的核型分析结果有误。他至少将第4对染色体的着丝点位置辨认错了。该对染色体不具有中部着丝点而实际上具有近端部着丝点。本文还比较了铁破锣和角叶铁破锣的核型差异,并详细讨论了铁破锣属的系统位置。     

山扁豆的染色体核型分析

目的:对辽宁分布的植物山扁豆的染色体数目、核型、体积等进行了研究.方法:采用常规制片方法,结合显微摄影对染色体进行统计分析.结果:山扁豆体细胞染色体数目2n=16, 相对长度组成2n=16=2L+4M2+10M1; 核型公式为K(2n)=2X=16=6m+6sm+4T; 全体染色体总长16.45 μm, 长臂总长11.81 μm,核型不对称系数(AS.K%)为71.9%,属于"3A"型,全体染色体总体积为17.04 μm3.结论:山扁豆体细胞染色体的数目、核型、体积等清晰准确,可为进一步的深入研究打下基础.     

五叶风藤茎尖染色体核型分析

用五叶风藤 (HolboelliafargesiiReaub)茎尖染色体制片 ,研究其染色体组型 ,结果表明 :五叶风藤的染色体组型公式为 2n =2x =16 =12m 4sm ,染色体基数x =8,第 4号染色体上有一对染色体随体 ,核型为 2B类型 ,其中 2n =4x =32 =2 4m 8sm的四倍性细胞相当普遍。     

毛莨在江西的核型变异

本文报道了毛茛(Ranunculus japonicus Thunb．)在江西发现的核型变异。R．japonicus 的基本核型为2n=14=6m+4sm十4st (2SAT);变异核型为2n=14十1B=6m+4sm+4st (2SAT)十1B和2n=14=6m+6sm(2SAT)+2st。核型变异表现在增加B染色体或第4对同源染色体异形及第6对随体染色体臂比变化。     

Investigation of the mechanism of temperature sensitivity of the electroreceptors of ampullae of lorenzini

In experiments on Black Sea skates (Raja clavata), the potential of the receptor epithelium of the ampullae of Lorenzini and spike activity of single nerve fibers connected to them were investigated during electrical and temperature stimulation. Usually the potential within the canal was between 0 and –2 mV, and the input resistance of the ampulla 250–400 k. Heating of the region of the receptor epithelium was accompanied by a negative wave of potential, an increase in input resistance, and inhibition of spike activity. With worsening of the animal's condition the transepithelial potential became positive (up to +10 mV) but the input resistance of the ampulla during stimulation with a positive current was nonlinear in some cases: a regenerative spike of positive polarity appeared in the channel. During heating, the spike response was sometimes reversed in sign. It is suggested that fluctuations of the transepithelial potential and spike responses to temperature stimulation reflect changes in the potential difference on the basal membrane of the receptor cells, which is described by a relationship of the Nernst's or Goldman's equation type.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. I. M. Sechenov, Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Pacific Institute of Oceanology, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 67–74, January–February, 1980.     

Principles of organization and evolution of systems of regulation of functions

Evolution of living organisms is closely connected with evolution of structure of the system of regulations and its mechanisms. The functional ground of regulations is chemical signalization. As early as in unicellular organisms there is a set of signal mechanisms providing their life activity and orientation in space and time. Subsequent evolution of ways of chemical signalization followed the way of development of delivery pathways of chemical signal and development of mechanisms of its regulation. The mechanism of chemical regulation of the signal interaction is discussed by the example of the specialized system of transduction of signal from neuron to neuron, of effect of hormone on the epithelial cell and modulation of this effect. These mechanisms are considered as the most important ways of the fine and precise adaptation of chemical signalization underlying functioning of physiological systems and organs of the living organism