168 resultados para 146-892D
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目的本研究以模式动物斑马鱼为研究对象,通过研究超重下鱼体的早期发育和耳石变化,探讨了脊椎动物前庭系统对超重环境的适应机制。方法斑马鱼受精卵在受精后10h分别置于1G和5G重力环境中,观察鱼体发育状态和耳石的形态;使用Zeiss软件比较1G和5G下耳石大小;使用EDAX检测耳石微化学成分含量变化。结果1)斑马鱼从鱼卵向早期仔鱼发育过程中超重环境影响仔鱼发育,耳石形态在初期显著变大(P<0.01),其后耳石变小;2)EDAX检测表明,耳石中S和Sr含量升高,Na和Ca的含量减少;3)出现矢耳石与微耳石融合的现
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在蓝藻水华形成以后,通过围隔实验,从2003年6月份到10月份定期采样测定水体中的pH、溶解氧(DO)、水温、总铁、亚铁、过滤性铁(<0.45μm)和可溶性磷的浓度,研究物化因子对不同形态铁浓度变化的影响。实验结果表明,蓝藻水华优势种微囊藻在pH 7—9和水温17.5—20.5℃的条件下,生长旺盛,消耗了大量的亚铁,使亚铁浓度大幅度下降;溶解氧和磷酸盐对亚铁浓度没有显著影响;在水华蓝藻严重发生的条件下,水体中的总铁和过滤性铁浓度没有显著意义的变化,而亚铁浓度的变化与水华蓝藻的种群密度成显著负相关(r=-0
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在滇池沿岸的池塘中 ,构建了面积为 10 0m2 ,水深为 85cm ,底质均为淤泥的四个围隔 ,其中在三个围隔内分别放养密度为 10 0g/m3 、75g/m3 、5 0g/m3 的鲢。它们均在一定程度上控制浮游植物的生物量并改善水体透明度 ,其中初始放养鲢 75g/m3 的围隔控制效果最明显。放养三种密度的鲢在有效控制微囊藻水华的同时 ,原先水体的优势种类发生质的变化 ,水体中浮游植物的多样性也明显增加。放鱼 2个月后 ,在生物操纵的围隔中同时种入菹草 ,在75g/m3 的鲢控藻的围隔中 ,菹草长势良
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在保安湖一围栏区 ( 3.3hm2 )周年采样 ,共获得可供食性分析用的二龄河蟹 36 2只 (壳宽 1.99— 6 .2 4cm)。胃含物分析表明 ,河蟹为杂食性 ,兼具肉食性倾向 ,以底层群落为食 ,食谱极为复杂 ,包括水生大型植物、藻类 ( 47个属 )、原生动物、轮虫、节肢动物、环节动物、软体动物、鱼类和颗粒碎屑 ,各大类食物的出现频率分别为 87.3%、82 %、0 .3%、0 .6 %、48.2 %、2 8.2 %、0 .3%、2 8.7%、88.7%。而不可分辨物在食物团中较为常见 ,出现频
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研究了从天然蓝藻水华藻粉中提微囊藻毒素,以及对提取物纯化的方法。通过对比不同提取剂的提取效果,发现浓度为80%的甲醇溶液提取效率最高,但采用乙醇作为替代提取剂也有较好的效率,且方法更为安全。对于提取物的纯化,可通过调节溶剂的pH至等电点以除去对反相填料具有负作用的藻胆蛋白。研究结果为更高效地纯化微囊藻毒素提供了依据。
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鲤具鲤科咽齿个体发生的共同性征,又呈现其种的独特性状。主要特性:(1)主列齿相连3齿胚几乎同时出现、同时脱落,形成3个相连齿种同时置换的特殊模式;(2)主列齿发生中曾出现4枚齿,替换3代后A_4齿退化消失,最终齿式1.1.3-3.1.1,成为迄今3列咽齿的鱼类中齿数最少的种类。鲤与其近缘种间系统关系比较结果:依最近缘属顺次排列为中鲤、原鲤、肥鲤;而最近缘的亚科为肥亚科。
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盐泽螺旋藻(Spirulina subsalsa)的水溶性色素粗提物经过硫酸铵沉淀和羟基磷灰石(HA)柱层析后可以分出两种藻胆蛋白,即藻蓝蛋白(c-PC)和别藻蓝蛋白(APC)。它们的纯度(指其在可见光部分的最大吸收与280nm处吸收之比)可分别达到7.27(c-PC)和6.55(APC)。而一般认可的纯度标准,PC为5,APC为6。纯化后的c-PC和APC在聚丙烯酰胺凝胶电泳(PAGE)中仅见一条色带,其最大吸收峰分别在620_(nm)和650_(nm),其室温荧光发射峰分别为642_(nm)和657_
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<正> 一、前言黑龙江是我国四大河流之一,位于我国东北边境,上游有额尔古纳河和石勒喀河,汇合后从西北向东南蛇行,是中苏两国的天然分界线。与乌苏里江汇合后,下游全部流经苏联境内,注入鄂霍次克海。为了开发黑龙江的水力资源,中苏两国于1956年开始,进行综合考察。浮游动物的调查研究是渔业小队工作的一个组成部分。工作共进行两年,1957年工作着重于黑龙江流域各个水体中浮游动物普查,工作地区包括黑龙江、松花江、嫩江、达赖湖、镜泊湖、兴凯湖及五大连池。在各个水体中采集了定性标本,并在7月和8月在黑河和哈尔滨两地做
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The ontogeny of IgM-producing cells was studied in juvenile mandarin fish Simperca chuatsi, an important fish in China's aquaculture sector. The IgM-producing cells were localised through in situ hybridisation with a probe complementary to the Ig mu-chain in lymphoid-related tissues, including head kidney, spleen, thymus, intestine and gills. In head kidney, transcripts of Ig mu were first detected at 20 days post-hatching (dph) with a few positive signals. and the number of IgM-producing cells increased obviously from 39 dph onwards. At 136 dph, a large amount of positive cells were observed in the entire organ with clusters of these cells located around the blood vessels. In spleen, IgM-producing cells were found from 26 dph onwards, followed by an increase until 67 dph: clusters of positive cells were also detected around blood vessels at 102 dph. In thymus, IgM-producing cells were first observed at 39 dph; thereafter, no obvious increase was detected until 78 dph. The positive cells in thymus were distributed mainly in the outer zone of thymus. A few IgM-producing cells were still observed in thymus of 1-year-old mandarin fish. IgM-producing cells were not detected in the intestine until 87 dph, with several discrete positively stained cells distributed in the lamina propria. IgM-producing cells, scattered mainly in primary gill filaments around blood vessels, were detected in gills from 90 dph. As in other teleosts, these results indicated that the head kidney appears to be the primary organ for IgM production in mandarin fish, and IgM-producing cells exist in all organs examined in the present study, implying their lymphoid role in fish. In addition, it is suggested that vaccination after 20 dph may be much more effective in mandarin fish. (C) 2009 Elsevier B.V. All rights reserved.
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An incubation experiment was performed on Potamogeton crispus (P. crispus) using sediment collected from Lake Tangxunhu in the center of China, in order to determine the effects of plant growth on Fe, Si, Cu, Zn, Mn, Mg, P, and Ca concentrations in the sediments and overlying waters. After 3 months of incubation, Ca, Mg, and Si concentrations in the water column were significantly lower, and P and Cu concentrations were significantly higher than in unplanted controls. The effect of P. crispus growth on sediment pore waters and water-extractable elements varied. Concentrations of Ca, Mg, Si, Fe, Cu, and Zn were significantly higher, and P was significantly lower, than in pore waters of the control. Water-extracted concentrations of Fe, Mg, and Si in the sediments were lower, and P was higher, than in the control. Presence of P. crispus generally enhanced concentration gradients of elements between pore waters and overlying waters but not for P. The growth of P. crispus was associated with an increase in water pH and formation of root plaques, resulting in complex effects on the sediment nutritional status.
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Two strains of Raphidiopsis Fritsch et Rich were isolated from a fishpond in Wuhan city, China and rendered axenic, and characterized by a combination of morphological, physiological, biochemical and genetic methods. Morphologically the strains were identified as Raphidiopsis mediterranea Skuja (straight trichomes) and R. curvata Fritsch et Rich (coiled trichomes). These two strains demonstrated slight differences in optimal temperature range and GC content, while sharing some common characteristics including inability to grow hetertrophically, similar salinity tolerance (up to 0.78%) and an identical fatty acid composition. Cyanotoxins were not found in the strain of R. mediterranea, however, the strain of R. curvata contained both deoxycylindrospermopsin and cylindrospermopsin. Phylogenetic affiliations inferred from 16S rRNA gene sequences demonstrated that both Raphidiopsis strains clustered with Cylindrospermopsis, demonstrating their phylogenetic ties to Nostocaceae. (c) 2007 Elsevier B.V. All rights reserved.
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Interferon (IFN)-regulatory transcription factor-1 (IRF-1) has been studied in mammals and fish but little is known about the relationship between its gene structure and nuclear 'ion of IRF-1 protein. In this study, a cDNA encoding Carassius auratus IRF-1 (CaIRF-1) was isolated from an interferon-producing cell line, C. ouratus blastulae embryonic (CAB) cells, exposed to UV-inactivated grass carp hemorrhagic virus (GCHV). The CaIRF-1 genomic locus exhibits exon-intron arrangements similar to those of other vertebrate IRF-1 loci, with nine exons and eight introns, although together with pufferfish IRF-1, CaIRF-1 distinguishes itself from other vertebrate IRF-1 genes by a relatively compact genomic size. Similar to the known IRF-1 genes, CaIRF-1 is ubiquitously expressed, and is upregulated in vitro and in vivo in response to virus, Poty I:C, or CAB INF-containing supernatant (ICS). Subcellular localization analysis confirms the nuclear distribution of CaIRF-1 protein, and reveals two nuclear localization signals (NILS), any one of which is sufficient for nuclear translocation of CaIRF-1. One NLS Locates to amino acids 117-146, and appears to be the structural and functional equivalent of the NLS in mammalian IRF-1. The second NLS (amino acids 73-115) is found within the DNA-binding domain (DBD) of CaIRF-1, and contains two regions rich in basic amino acids (''(KDKSINK101)-K-95" and ''(75)KTWKANFR(82)"). In comparison with mammalian IRF-1, in which the corresponding amino acid stretch does not seem to drive nuclear translocation, five conserved basic amino acids (K-75, K-78, R-82, K-95, and K-101) and one non-conserved basic amino acid (K-97) are present in this NLS from CaIRF-1. This observation suggests that K97 Of CaIRF-1 might be essential for the function of its second NLS, wherein the six basic aminoacids might cooperate to drive CaIRF-1 to the nucleus. Therefore, the current study has revealed a new nuclear localization motif in the DBD of a vertebrate IRF-1. (C) 2007 Elsevier Ltd. All rights reserved.
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The seasonal variations of estrogenic compounds and the estrogenicities of influent and effluent were investigated by OF chemical analysis and in vitro assay in a municipal sewage treatment plant in Wuhan (China). The levels of eight estrogenic compounds, including 17 beta-estradiol (E-2) estrone (E-1), estriol (E-3) diethylstilbestrol (DES), 17 alpha-ethinylestradiol, nonylphenol (NP), 4-tert-octylphenol (OP), and bisphenol A (BPA), were measured by gas chromatography-mass spectrometry. Total estrogenic activity of sewage was quantitatively assessed using primary cultured hepatocytes of male Megalobrama amblycephala Yih using vitellogenin as a biomarker. The E-2 equivalents (EEQs) obtained from the chemical analysis were consistent with those measured by bioassay. The natural (E-1, E-2, and E-3) and synthetic (DES) estrogens, as well as NP, were the main contributors of the total EEQs of influent and effluent in the present study. The levels of natural estrogens E-1 and E-3 in the influent and effluent were higher in winter than in summer, whereas the situation for NP and OP was the reverse. The levels of E-2, DES, and BPA varied little among different seasons. 17 alpha-Ethinylestradiol was not detected in the influent and effluent. The estrogenicities of the influent and of the primary and secondary effluents were all higher in summer than in winter. Estrogenic activities in winter mainly originated from natural (E-1, E-2, and E-3) and synthetic (DES) estrogens, whereas the increase of EEQs in summer was contributed by NP The results from chemical analysis and bioassay demonstrate that estrogenic compounds cannot be entirely removed by the existing sewage treatment process, which should be further improved to protect aquatic ecosystems and human health.
A new fluorescent quantitative PCR-based in vitro neutralization assay for white spot syndrome virus
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A fluorescent quantitative PCR (FQ-PCR) assay utilizing SYBR green I dye is described for quantitation of white spot syndrome virus (WSSV) particles isolated from infected crayfish, Cambarus clarkii. For this assay, a primer set was designed which amplifies, with high efficiency and specificity, a 129 bp target sequence within ORF167 of the WSSV genome. Conveniently, WSSV particles can be added into the FQ-PCR assay with a simple and convenient method to release its DNA. To establish the basis for an in vitro neutralization test, primary cultures of shrimp cells were challenged with WSSV that had been incubated with a polyclonal anti-WSSV serum or with control proteins. The number of WSSV particles released from the cells after these treatments were assayed by FQ-PCR. This test may serve as a method to screen monoclonal antibody pools or recombinant antibody pools for neutralizing activity prior to in vivo animal experiments. (c) 2007 Elsevier B.V. All rights reserved.