990 resultados para 343-C0019C
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运用经典血清学方法首次在红鯽中证明了一种与金枪鱼中的A-B-O血型及人类的ABO血型模式相似的红细胞抗原系统,命名为S血型系统。该系统有四种血型表型:S~1,S~2,S~2S~2和S~0,推测它由S~1、S~2和S~0三个复等位基因决定。
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于1981年,以经过γ射线或紫外线处理的近类精子作为激活源,成功地诱发兴国红鲤(cyprinus carpio)卵子的雌核发育。经两代连续雌核发育的部分后代个体进行人工转性,使之成为“生理雄性”,并以“生理雄性”个体与其同胞姐妹交配所产后代为遗传特性纯一的个体——红鲤8305。检查了LDH,EST,MDH,SOD,IDH及运铁蛋白(transferrin)的座位,发现同一个系的不同个体之间等位基因没有差别,而且各座位的等位基因都是纯合的。血清学试验表明,控制红鲤8305雌核发育系的红细胞表面抗原的基因纯合
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以草鱼(Ctenopharyngodon idellus)为母本、鲤(Cyprinus carpio)为父本进行人工杂交,杂种胚胎发育至孵化期全部死亡;同时获得了少数雌核发育草鱼和雄核发育的鲤。分析比较了草鲤杂种胚胎染色体变化及胚胎发育情况。发现杂种胚胎染色体数目变化较大,一般在24—73之间,绝大部分细胞染色体在发育过程中不断丢失而出现非整倍体;极少数细胞在受精后雌性原核和雄性原核不结合而引起雌核发育和雄核发育;草鱼和鲤胚胎发育时序有较大差别;因此细胞分裂不能同步。可能是杂种胚胎染色体不断丢失的主要原因
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本项研究工作表明,塔式生物滤池在处理模拟洗涤剂工业废水时,能够适应和克服一般好氧生化法所不能解决的泡沫问题,并对废水中的LAS和COD具有一定的去除效果。根据实验结果,初步认为塔滤可应用于洗涤剂工业废水的生化处理,并向洗涤剂行业首次推荐这种废水生物学净化方法。从塔滤的生物膜中分离出了优势菌,经鉴定为一种气单胞菌(Aeromonas sp.D-4)。
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根据MacArthur-Wilson的岛屿区系平衡模型S_t=S_(eq)(1-e~(GT)),可以从野外生态效应试验和室内毒性试验中,提出3个功能参数(S_(eq)、G、t_(90%))进行比较。本文提出两种计算方法:复合梯形法和最小二乘法,后者已在计算机上实现了BASIC计算程序。从数学理论上论证,最小二乘法误差较小,但如果实验布局合理,两种计算方法能得到十分一致的结果。实验模型是否符合理论模型,可以用统计学上的拟合差异度检验法来检验。
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本文报导 1973年武汉市郊两个渔业高产湖塘的理化、生物环境特点,并分析了各类环境因素间的关系。在养殖季节中,湖水溶氧量通常在7毫克/升以上,总氮平均为2.63毫克/升,总磷平均为0.38毫克/升;浮游植物平均为2,199×10~4-3,080×10~4个/升,主要为硅藻,甲藻和绿藻等小型种类;浮游动物平均为39,200-74,318个/升,以原生动物和轮虫为主。文中提出了各类环境因素间相互关系的方程式,定量地描述了饵料生物丰度和氮、磷的关系。
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本文根据浮游植物生产量求得对鲢、鳙的供饵能力,并通过浮游植物对鲢、鳙转化效率的计算,估算出武昌东湖鲢、鳙的生产潜力,进而求得武昌东湖鲢、鳙的合理投放量。作者求得东湖浮游植物全年对鲢、鳙的供饵能力是61,153吨(鲜重);由此估算出东湖鲢、鳙的生产潜力是789公斤/公顷以上,每年鱼种(四寸以上)的合理投放量,鲢是 209万尾,鳙是 110万尾。
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<正> 一、绪言1958年9月—1959年9月在湖北黄石市北郊花马湖(鄂城县境)进行湖泥施肥试验,在室内、室外先后试验了35次,历时343天,在党的正确领导和全体工作人员的积极努力下,利用湖泥施肥的方法获得了成功。湖泊底泥里面,有腐烂的水草碎片、浮游植物及水生动物的尸体残骸等淤积;加之,由于雨水将地面冲下来的表层富有机质肥土也沉积于底部,因此,一般湖泊的底泥都很肥,常厚达0.5—1.0米以上;pH 值介于5.2—7.0间;无机酸度(以甲基橙作指示剂)为零,总酸度(以酚酞作指示剂)介于0.16—0.46毫克
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We investigated the age and growth of Schizothorax o'connori in the Yarlung Tsangpo River by examination of annuli from otoliths. The von Bertalanffy model was the most acceptable statistical growth model. Its parameters were as follows: SL infinity = 492.4 mm, K = 0.1133, t(0) = -0.5432 year and W-infinity = 1748.9 g for females; SL infinity = 449.0 mm, K = 0.1260, t(0) = -0.4746 year and W-infinity = 1287.0 g for males. Theoretical longevity was 25.9 years for the female and 23.3 years for the male. Moreover, females had larger asymptotic length and weight compared with males.
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The gene of piscidin, an antimicrobial peptide, has been cloned from the mandarin fish, Siniperca chuatsi. From the first transcription initiation site, the mandarin fish piscidin gene extends 1693 nucleotides to the end of the 3' untranslated region and contains four exons and three introns. A predicted 79-residue prepropeptide consists of three domains: a signal peptide (22 aa), a mature peptide (22 aa) and a C-terminal prodomain (35 aa). The shortage of XQQ motif in the prodomain of mandarin fish piscidin and the similar gene structure between moronecidins (piscidins) and pleurocidins may indicate that they are derived from the same ancestor gene. We thus suggest that piscidin should be used as a terminology for these antimicrobial peptides in the future. The mandarin fish piscidin mRNA was abundant in intestine, spleen, pronephros and kidney analysed by real-time polymerase chain reaction. After stimulation with lipopoly saccharides (LPS), a marked increase in transcripts was observed in most tissues, indicating that piscidin is not only a constitutively expressed molecule, but also has an increased response to bacterial infection. The synthetic, amidated mandarin fish piscidin exhibited different antimicrobial activity against different fish bacterial pathogens, especially against species of Aeromonas, which may to certain extent reflect the pathogenicity of these bacteria.
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Anabaena sp. PCC; 7120 was mutagenized by transposon Tn5-1087b, generating a mutant whose heterocysts lack the envelope polysaccharide layer. The transposon was located between nucleotides 342 and 343 of alr0117, a 918 bp gene encoding a histidine kinase for a two-component regulatory system. Complementation of the mutant with a DNA fragment containing alr0117 and targeted inactivation of the gene confirmed that alr0117 is involved in heterocyst development. RT-PCR showed that alr0117 was constitutively expressed in the presence or absence of a combined-nitrogen source. hepA and patB, the two genes turned on during wild-type heterocyst development, were no longer activated in an alr0117-null mutant. The two-component signal transduction system involving alr0117 may control the formation of the envelope polysaccharide layer and certain late events essential to the function of heterocysts.
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This paper describes the long-term dynamics of phosphorus concentrations in both the lake water and the sediment in a subtropical Chinese lake, Lake Donghu. The total phosphorus (TP) concentration in the lake water experienced an upward trend from the 1950s, and peaked in 1983/1984, but declined obviously afterwards. From the 1950s to the 1990s, TP content in the upper 10 cm sediment of the lake increased steadily from 0.307 to 1.68 mg Pg DW-1 at Station I and from 0.151 to 0.89 mg Pg DW-1 at Station II, respectively. The TP increase in the lake water before mid-1980s was mainly attributed to the massive input of sewage P. The outbreak of cyanobacterial blooms coincided with the peaks of TP and Orthophosphate (PO4-P) in the water in mid-1980s, and the maximum TP of the water reached as high as 1.349 mg/1 at Station I and 0.757 mg/l at Station II (in 1984), respectively. The declines of TP and PO4-P in the water after mid-1980s was coincident with the disappearance of cyanobacterial bloom. (C) 2001 Elsevier Science Ltd. All rights reserved.
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Resting metabolism was measured in immature mandarin fish Siniperca chuatsi weighing 42.1-510.2 g and Chinese snakehead Channa argus weighing 41.5-510.3 g at 10, 15, 20, 25, 30 and 35 degreesC. Heat increment of feeding was measured in mandarin fish weighing 202.0 (+/-14.0) g and snakehead weighing 200.8 (+/-19.3) g fed swamp leach Misgurnus anguillicaudatus at 1% body weight per day at 28 degreesC. In both species, weight exponent in the power relationship between resting metabolism and body weight was not affected by temperature. The relationship between resting metabolism and temperature could be described by a power function. The temperature exponent was 1.39 in mandarin fish and 2.10 in snakehead (P < 0.05), indicating that resting metabolism in snakehead increased with temperature at a faster rate than in mandarin fish. Multiple regression models were used to describe the effects of body weight (W, g) and temperature (T, C) on the resting metabolism (R-s, mg O-2/h): In R-s = - 5.343 + 0.772 In W + 1.387 In T for the mandarin fish and In R-s = -7.863 + 0.801 ln W + 2.104 In T for the Chinese snakehead. The proportion of food energy channelled to heat increment was 8.7% in mandarin fish and 6.8% in snakehead. (C) 2000 Elsevier Science Inc. All rights reserved.
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A series of hydrogenated amorphous silicon carbide (a-Si1-xCx:H) films were prepared by plasma-enhanced chemical vapour deposition (PECVD) using a gas mixture of silane, methane, and hydrogen as the reactive source. The previous results show that a high excitation frequency, together with a high hydrogen dilution ratio of the reactive gases, allow an easier incorporation of the carbon atoms into the silicon-rich a-Si1-xCx:H film, widen the valence controllability. The data show that films with optical gaps ranging from about 1.9 to 3.6 eV could be produced. In this work the influence of the hydrogen dilution ratio of the reactive gases on the a-Si1-xCx:H film properties was investigated. The microstuctural and photoelectronic properties of the silicon carbide films were characterized by Rutherford backscattering spectrometry (RBS), elastic recoil detection analysis (ERDA), and FT-IR spectrometry. The results show that a higher hydrogen dilution ratio enhances the incorporation of silicon atoms in the amorphous carbon matrix for carbon-rich a-Si1-xCx:H films. One pin structure was prepared by using the a-Si1-xCx:H film as the intrinsic layer. The light spectral response shows that this structure fits the requirement for the top junction of colour sensor. (c) 2004 Elsevier B.V. All rights reserved.