246 resultados para 142
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863计划资助(2002AA601021); 973计划(2002CB412309)资助
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通过 4周的生长实验 ,研究了Ⅰ龄暗纹东方 (82 35± 2 97g)在不同盐度预处理后的摄食、生长和饲料利用情况。结果显示 :35‰的预处理盐度对暗纹东方的生长有抑制作用 ,当这种盐度胁迫解除后 ,暗纹东方的生长表现出明显的补偿现象。本实验中摄食率随前处理盐度的升高而增加 ,变化范围为 1 83%— 2 5 1% ,特定生长率亦随前处理盐度增加而增加 ,即由 0 83%增加到 1 2 8% ,饵料系数则随前期盐度实验中盐度的增加而降低 ,由 1 6 7降至 1 4 7。在盐度预处理实验及淡化养殖
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DNA指纹个体识别技术是保护遗传学研究中的一种非常重要的手段。为了准确地识别天鹅洲保护区中的每一头长江江豚以开展保护遗传学及其它相关研究 ,并实施有效的种群管理 ,本研究应用 4个微卫星座位初步构建了该群体的DNA指纹图谱 ,并利用此图谱成功地对不同时期在保护区捕获的江豚进行了个体识别研究。结果显示微卫星指纹技术是一种适用于长江江豚个体识别研究的可靠手段
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研究了两种微囊藻毒素在两种紫外光照射下的光降解行为 ,研究结果表明 :UV C是降解微囊藻毒素较好的光源 ;光照强度是影响毒素降解重要的因素 ,其次是温度和酸度 ;在UV C的照射下 ,水体腐殖质对光降解具有抑制作用 ;微囊藻毒素的光解反应符合准一级动力学模型 .同时本工作还按实际环境水体中毒素的含量水平进行了模拟研究 ,发现紫外光UV C对环境水体中低含量的微囊藻毒素具有很强的去除能力 .为今后发展无毒、高效、经济实用的饮用水处理技术做了有益的探索 .
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通过对鲤形目鱼类 5个科的代表类群的完整线粒体 12SrRNA进行测序和分析 ,以检验目前的形态学假说。经序列比对后 ,有 10 0 0个位点 ,其中 467个位点在茎区 ,53 3个在环区 ;有 3 95个位点为变化位点 ,其中 2 67个为系统发育信息位点。采用邻接法和最大简约法进行了系统发育分析 ,其结果支持鲤科鱼类成为一个单系群 ,非鲤科的鲤形目鱼类成为另一个单系群的观点 ,这与Siebert提出的假说相一致。鲤科鱼类包含 3个主要的分支 ,即鱼丹系、鲤系和雅罗鱼系 ;但在非鲤科鲤形目鱼类中 ,其
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对秦岭西段汉江水系和嘉陵江水系的鱼类和环境调查显示 ,人类活动对鱼类多样性产生了较大的影响。本文试图对该地区鱼类多样性丧失的现状加以报道并对原因进行分析。以前该地区鱼类共有 142种 ,本次调查的渔获物中只有 34种。鱼类物种资源的减少是多种因素造成的 :水坝的修建使得鱼类栖息地环境改变从而导致鱼类的种类和种群数量变化 ,水污染、过度捕捞和非法渔业也在一定程度上破坏了鱼类物种多样性。
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本文研究了一浅水草型湖泊──扁担塘中桡足类的群落结构,包括种类组成、种群动态及现存量。在一周年的研究中,共发现14种浮游桡足类(9种剑水蚤和5种哲水蚤)。根据年平均密度,剑水蚤的优势种为:Mesocyclops notius,Cyclops vincinuis vincinus和Thermocyclops brevifurcatus,而哲水蚤的优势种为Meodiaptomus yantsekiangensis和Sinocalanus dorrii。通过比较长江沿岸的5个湖泊的桡足类的种类组成发现,桡足类的
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通过DEAE-纤维素柱层析分级分离可将柱孢鱼腥藻(Anabaena cylindrica)固氮酶铁蛋白组分纯化21倍,比话性达142.46nmolC_2H_4/mg蛋白·分。纯化的铁蛋白质用聚丙烯酰胺凝胶电泳鉴定呈均一状态,分子量约为61,000。氨基酸组分分析的结果不含色氨酸,而酸性氨基酸中天门冬氨酸和谷氨酸的含量占氨基酸总数的22%,约为碱性氨基酸中精氨酸和赖氨酸的2.6倍。用原子吸收分光光度计测定不含钼,每个铁蛋白分子中平均含有3.36原子的铁。柱孢鱼腥藻固氮酶钼铁蛋白与铁蛋白的滴定试验表明,钼铁蛋
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根据囊胚细胞和原肠胚细胞染色体数的观察,三倍体雄性方正银鲫 Carassius auratusgihelio)和二倍体雌性红鲫(Carssius auratus red variety)杂交获得的胚胎,是杂合的非整倍体胚胎,因此胚胎发育畸形,中途死亡。胚胎染色体数从50至142,变异幅度很宽,86%以上胚胎细胞染色体数分布在56—105范围内,其中以染色体数为76—86的胚胎细胞最常见,占34%。
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Successful applications of expanded bed adsorption (EBA) technology have been widely reported in the literature for protein purification. Little has been reported on the recovery of natural products and active components of Chinese herbal preparations using EBA technology. In this study, the hydrodynamic behavior in an expanded bed of cation resin, 001 x 7 Styrene-DVB, was investigated. Ephedrine hydrochloride (EH) was used as a model natural product to test the dynamic binding capacity (DBC) in the expanded bed. EBA of EH directly from a feedstock containing powdered herbs has also been investigated. These particles are different from commercially available expanded bed adsorbents by virtue of their large size (20S to 1030 gm). When the adsorbent bed is expanded to approximately 1.3 to 1.5 times its settled bed height, the axial liquid-phase dispersion coefficient was found to be of the order 10(-5) m(2) s(-1), which falls into the range 1.0 x 10(-6) to 1.0 X 10(-5) m(2) s(-1) observed previously in protein purification. Because of the favorable column efficiency (low axial dispersion coefficient), the recovery yield and purification factor values of EH directly from a feedstock reached 86.5% and 18, respectively. The results suggest that EBA technology holds promise for the recovery of natural products and active components of Chinese herbal preparations.
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Toxicity of many waterborne organic contaminants to aquatic organisms is mediated through oxidative damages resulting from the production of reactive oxygen species (ROS). Using duroquinone as a model ROS inducer, we carried out in vitro and in vivo experiments to test the hypothesis that reproduction in common carp (Cyprinus carpio) can be impaired through oxidative damage of their spermatozoa. In vitro exposure of fish spermatozoa to 0, 12.5, 25, 50, 100 and 200 mu M duroquinone for 2 h showed a significant increase in the level of ROS in a dose-dependant manner. Sperm motility was significantly reduced in all exposure groups, but lipid peroxidation (LPO) and DNA strand break (measured by comet assay) were only enhanced at 50 mu M and above. A significant decrease in subsequent hatching rate was recorded in all the exposure groups, despite fertilization rate was not affected. In the in vivo experiment, spermatozoa were collected 24 and 72 h after fish received intra-peritoneal injections of 1.0 and 10 mg kg(-1) body weight duroquinone. DNA damage was clearly evident in spermatozoa of all treatment groups after 72 h exposure, and ROS was significantly enhanced in the high concentration group. LPO however, remained unchanged in both treatment groups. The overall results of both our in vitro and in vivo experiments demonstrated that duroquinone can induce ROS production in spermatozoa, which may impair sperm quality and subsequently reproductive success through oxidative stress. (c) 2006 Elsevier B.V. All rights reserved.
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Mature female and male zebrafish were separated and exposed to nonylphenol (NP) at 0.1, 1, 10, 50, 100 and 500 mu g/L, respectively, for 3 weeks. Gonadosomatic index (GSI) in both sexes and vitellogenin (VTG) induction in males was measured as the bioindicators for the impairment to the parents. The results indicated that 50 mu g/L of NP was the non-observed effect concentration (NOEC) for GSI and VTG induction. Afterwards, the 50 mu g/L NP exposed females and males, and the control females and males were cross-wise pair-bred in the control water for one week to examine the reproductive effects. The embryonic cathepsin D (CAT D) activity, eggshell thickness, fecundity, hatching rate and malformation (vertebral column flexure) rate of offspring were determined in the four pair-bred groups. While endpoints remained unchanged in the groups with exposed males, prenatal exposure of females to 50 mu g/L of NP resulted in the impairment of reproduction in groups with exposed females including inhibition of CAT D activity (P < 0.05), decrease of eggshell thickness (by 23.6%) and elevation of malformation rate (P < 0.001). These results suggested NP could induce reproductive damage to zebrafish at NOEC for parents. The results also imply that alterations of CAT D activity and eggshell thickness may be more sensitive biomarkers to indicate the reproductive effects caused by endocrine disrupting chemicals. (c) 2005 Elsevier Inc. All rights is reserved.
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A novel fish-specific apolipoprotein (apo-14 kDa) has been recently cloned from eel and pufferfish. However, its expression pattern has not been elucidated. in this study, EcApo-14 has been screened from hypothalamic cDNA library of male orange-spotted grouper, which shows 62.9%, 51%, 46.9%, 43.2%, and 31.9% identities to Apo-14 of European flounder, pufferfish, Japanese eel, gibel carp, and grass carp, respectively. RT-PCR analysis reveals that this gene is first transcribed in neurula embryos and maintains a relatively stable expression level during the following embryogenesis. EcApo-14 transcripts are at a very high level during embryonic and early larval development in the yolk syncytial layer (YSL), and decrease in YSL and form intense staining in liver at 3 days after hatching. In adult tissues, EcApo-14 is predominantly expressed in liver and brain. The data suggested that EcApo-14 might play an important role in liver and brain morphogenesis and growth. (c) 2005 Elsevier Inc. All rights reserved.
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An 8-week growth trial investigated the effect of dietary lipid level on growth performance of a carnivorous fish, Chinese longsnout catfish (Leiocassis longirostris Gunther) and an omnivorous fish, gibel carp (Carassius auratus gibelio). For each species, seven isonitrogenous semi-purified diets (455 g kg(-1) crude protein for Chinese longsnout catfish and 385 g kg(-1) crude protein for gibel carp) were formulated to contain 30, 60, 90, 120, 150, 180 or 210 g kg(-1) lipid. For Chinese longsnout catfish, feed intake (FI) decreased with increasing dietary lipid and there was no significant difference in feed intake from 90 to 210 g kg(-1) lipid. Specific growth rate (SGR) increased with dietary lipid level (P < 0.05) and the 150 and 180 g kg(-1) groups were the best. Feed conversion efficiency (FCE), protein retention efficiency (PRE) and energy retention efficiency (ERE) were higher at 180 g kg(-1) lipid. For gibel carp, FI decreased with increased dietary lipid and 180 and 210 g kg(-1) lipid groups showed lower values. SGR increased with dietary lipid level and the 150 and 180 g kg(-1) were the best. FCE was higher at 180 g kg(-1) lipid level. PRE increased with dietary lipid level and there was no significant difference in groups from 120 to 210 g kg(-1) dietary lipid. ERE increased with increasing dietary lipid level, and groups fed 120, 150 and 180 g kg(-1) lipid showed the highest values. In Chinese longsnout catfish, increase in dietary lipid level, resulted in increased carcass dry matter, crude protein, crude lipid and gross energy. In gibel carp, dry matter, crude protein, and crude lipid increased with dietary lipid level. Based on regression between SGR and dietary lipid, dietary lipid requirements for Chinese longsnout catfish and gibel carp were 142.6 and 140.5 g kg(-1), respectively.
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Photolysis of microcystins by UV irradiation and the effects of different environmental factors on efficiency of UV degradation were studied. The results indicated that the rates of the photolytical degradation reactions of microcystin-LR and RR-follow pseudo-first-order kinetic process. The results also showed that the concentrations of two microcystin variants decreased significantly by UV-C Irradiation; the wavelength and intensitiy of UV irradiation are two very important factors affecting the rate of degradation; temperature and pH value could also affect the half life of degradation rates. When irradiated by weaker UV-Iight, isomerization could be detected in the course of photolytical degradation. The concentrations of two isomers transformed from microcystin-LR reached its maximum at the third minute and decreased with the time afterwards. To simulate photolysis of microcystins in the field water body, microcystins with low concentration were used. It was found that UV-C illumination was capable of decomposing over 95% of microcystins within 40 min. In the presence of humic substances the photodecomposition slowed down to a certain extent. These results are valuable in using UV irradiation for elimination microcystins from raw water.