953 resultados para MERCURY LAMP


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General equations of the electrocatalytic reaction at an ultramicroelectrode modified with redox species have been described according to the Andrieux Saveant model. The electrocatalytic kinetic process has been discussed for the whole set of cases, ie (R), (R + S), (SR) (SR + E), (E), (R + E), (ER), (S), (ER + S) and (S + E) limiting situations. The effect of gamma on the catalytic steady state current shows that the higher the value of gamma, the lower the catalytic current. The kinetic process shifts rapidly from R to E with increasing values of gamma. It is favorable for catalysis only when gamma is very low. Therefore, the redox species modified ultramicroelectrode with thin film is utilized for electrocatalysis, and the larger the radius of ultramicroelectrode, the higher the catalytic efficiency.

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The analytical expressions of quasi-first and second order homogeneous catalytic reactions with different diffusion coefficients at ultramicrodisk electrodes under steady state conditions are obtained by using the reaction layer concept. The method of treatment is simple and its physical meaning is clear. The relationship between the diffusion layer, reaction layer, the electrode dimension and the kinetic rate constant at an ultramicroelectrode is discussed and the factor effect on the reaction order is described. The order of a catalytic reaction at an ultramicroelectrode under steady state conditions is related not only to C(Z)*/C(O)* but also to the kinetic rate constant and the dimension of the ultramicroelectrode; thus the order of reaction can be controlled by the dimension of the ultramicroelectrode. The steady state voltammetry of the ultramicroelectrode is one of the most simple methods available to study the kinetics of fast catalytic reactions.

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The current equation of the electrocatalytic reaction at a microdisk electrode modified with redox species has been described and verified experimentally. There exists a linear relationship between plateau limiting current and the radius of the microdisk electrode for a catalytic process. The influence of the dimensions of the microdisk electrode on catalytic efficiency is discussed. The polyvinylferrocene (PVFc)-modified microdisk electrode prepared by the coating method was taken as a typical example, on which the electrocatalytic oxidation of ascorbic acid could be studied. The catalytic reaction rate constants were determined as an average value of 1.5 X 10(-7) cm3/mol s by this method, and are consistent with those obtained at a conventional electrode.

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Electrodeposition process of polycrystalline Cd-rich Hg_(1-z)Cd_xTe (x>0.5) in acidic bath of CdSO_4+HTeO_2~+HgCl_2 was investigated. The simultaneous electrodeposition technique of three kinds of ions at the same potential has been achieved. The XRD, SEM and EDAX analysis of the thin film electrodeposited on titanium substrate showed a typical cubic zinc blende polycrystalline structure and homogeneous dispersion. The photoelectrochemical behavior of (1-x)=0.09 polycrystalline thin film in a polysulfide re...

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Tank cultivation of marine macroalgae involves air-agitation of the algal biomass and intermittent light conditions, i.e. periodic, short light exposure of the thalli in the range of 10 s at the water surface followed by plunging to low light or darkness at the tank bottom and recirculation back to the surface in the range of 1-2 min. Open questions relate to effects of surface irradiance on growth rate and yield in such tumble cultures and the possibility of chronic photoinhibition in full sunlight. A specially constructed shallow-depth tank combined with a dark tank allowed fast circulation times of approximately 5 s, at a density of 4.2 kg fresh weight (FW) m(-2) s(-1). Growth rate and yield of the red alga Palmaria palmata increased over a wide range of irradiances, with no signs of chronic photoinhibition, up to a growth-saturating irradiance of approximately 1600 mumol m(-2) s(-1) in yellowish light supplied by a sodium high pressure lamp at 16 h light per day. Maximum growth rate ranged at 12% FW d(-1), and maximum yield at 609 g FW m(-2) d(-1). This shows that high growth rates of individual thalli may be reached in a dense tumble culture, if high surface irradiances and short circulation times are supplied. Another aspect of intermittent light relates to possible changes of basic growth kinetics, as compared to continuous light. For this purpose on-line measurements of growth rate were performed with a daily light reduction by 50% in light-dark cycles of 1, 2 or 3 min duration during the daily light period. Growth rates at 10degreesC and 50 mumol photon m(-2) s- 1 dropped in all three intermittent light regimes during both the main light and dark periods and reached with all three periodicities approximately 50% of the control, with no apparent changes in basic growth kinetics, as compared to continuous light.

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Hsp70 proteins are a family of molecular chaperones that are involved in many aspects of protein homeostasis. In this study, an Hsp70 homologue (SoHsp70) was identified from red drum Sciaenops ocellatus and analyzed at molecular level. The open reading frame of SoHsp70 is 1920 bp and intronless, with a 5'-untranslated region (UTR) of 399 bp and a 3'-UTR of 241 bp. The deduced amino acid sequence of SoHsp70 shares 84-92% overall identities with the Hsp70s of a number of fish species. In silico analysis identified in SoHsp70 three conserved Hsp70 domains involved in nucleotide and substrate binding. The coding sequence of SoHsp70 was subcloned into Escherichia coli, from which recombinant SoHsp70 was purified and, upon ATPase assay, found to exhibit apparent ATPase activity. Expressional analysis showed that constitutive expression of SoHsp70 was detectable in heart, liver, spleen, kidney, brain, blood, and gill. Experimental challenges with poly(I:C) and bacterial pathogens of Gram-positive and Gram-negative nature induced SoHsp70 expression in kidney to different levels. Stress-responsive analysis of SoHsp70 expression in primary cultures of red drum hepatocytes showed that acute heat shock treatment elicited a rapid induction of SoHsp70 expression which appeared after 10 min and 30 min of treatment. Exposure of hepatocytes separately to iron, copper, mercury, and hydrogen peroxide significantly unregulated SoHsp70 expression in time-dependent manners. Vaccination of red drum with a Streptococcus iniae bacterin was also found to induce SoHsp70 expression. Furthermore, recombinant SoHsp70 enhanced the immunoprotective effect of a subunit vaccine. Taken together, these results suggest that SoHsp70 is a stress-inducible protein that is likely to play a role in immunity and in coping with environmental and biological stresses. (C) 2010 Elsevier Ltd. All rights reserved.

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The present paper deals with the distribution patterns of heavy metals and the associated influencing factors in the Yalu River Estuary and its adjacent coastal waters. Based upon the analysis of the surficial and core sediments measurements, the pollution of heavy metal and potential ecological risk were evaluated. The burial flux and contents of heavy metals (except for copper) have been continuously increasing since the 1920s. Therefore, the gross potential ecological risk for the sediments was high or very high, and the study area was endangered by heavy metals contamination. Heavy metals originated mainly from upstream pollutant input, correlation analysis showed that chromium, nickel, zinc, cadmium, lead, arsenic, and mercury in the sediments of the middle and west channels as well as the sea area of the western Yalu River Estuary concentrations were most probably derived from similar sources. In contrast, the metal of copper most probably originated from sources different from the other metals. Preliminary studies indicate that copper contamination was most likely the result of emission from mining activities situated at the upstream of the river. The contents of heavy metals in the sediments of estuarine turbidity maximum zone of Yalu River were larger than those of any other areas in the middle channel. With large portion of fine sediments, weaker hydrodynamics, and richer sources of heavy metals, the sediments of the west channel, were even more enriched with heavy metals than those of the middle channel.

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本论文基于对我国沿海重金属污染加剧以及滩涂贝类资源衰退现象的关注,围绕典型滩涂贝类四角蛤蜊生物化学、细胞生物学和免疫学特征开展研究,调查了渤海湾天津近岸海域四角蛤蜊体内重金属含量和分布规律,以及四角蛤蜊对沉积物重金属的富集能力。室内模拟研究了四角蛤蜊对重金属镉和汞的富集能力及同化机制(assimilation mechanism)差异性,四角蛤蜊各组织对镉和汞的解毒机理和负载能力,以及重金属胁迫对四角蛤蜊血细胞结构和功能的损伤效应。研究结果可望为探讨四角蛤蜊受重金属胁迫细胞水平上的响应机制,揭示重金属污染和贝类资源衰退的关系,建立快速可靠的重金属污染生物标志物指标体系,开展生态健康评估和生境修复等提供科学依据。主要研究结果如下: 1.查明了渤海湾天津近岸四角蛤蜊体内和表层沉积物中Cd、Pb、Cu、Zn、Mn、Cr和Ni七种重金属的含量和周年时空分布特征;表层沉积物中Cd具有较强的污染程度和潜在生态风险,四角蛤蜊对重金属元素Cd和Pb具有较高的富集能力,对环境重金属污染具有很好的指示作用。 2.查明了Cd对四角蛤蜊在24h,48h和96h的半致死浓度(LC50)分别为15.96mg/L、5.15mg/L和2.38mg/L,汞的24h,48h和96h LC50分别为3.71mg/L,0.61mg/L和0.21mg/L。镉和汞对四角蛤蜊的安全质量浓度分别为0.0238mg/L和0.0021mg/L。 3.四角蛤蜊软体部对Cd和Hg的富集能力有显著差异。暴露过程中,四角蛤蜊软体部Cd和Hg的增加量分别为0.12-7.7µg/g和0.002-0.024µg/g,富集率分别为0.3-6.2%和0.11-0.68%,吸收率常数分别为0.07-1.10和0.001-0.005。 4.四角蛤蜊受Cd和Hg胁迫后,外套膜、鳃和肝胰腺的金属硫蛋白(MT)含量均在暴露浓度和胁迫时间上都有极显著变化。组织内MT含量的大小关系为:肝胰腺>鳃>外套膜。肝胰腺可以作为双壳贝类MT重金属污染指示研究的目标组织。四角蛤蜊对Cd和Hg不同的解毒机制,导致组织中MT的表达含量和Cd胁迫显著相关,而与Hg胁迫无显著相关性。 5.四角蛤蜊肝胰腺和鳃中抗氧化系统酶、脂质过氧化产物、酸性磷酸酶(ACP)和碱性磷酸酶(ALP)在不同Cd胁迫浓度和暴露时间下有显著差异。与对照组相比,超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)的活力和丙二醛(MDA)含量均随着暴露时间的增加而增加,达到一个峰值,然后减低。而ACP和ALP活力则表现出先被抑制,然后升高的变化趋势。肝胰腺中CAT和GPx活力高于鳃,鳃中SOD和MDA含量高于肝胰腺,这种差异与两种组织不同的解毒机理有关。 6.重金属胁迫能够造成四角蛤蜊血细胞超微结构的损伤、溶酶体膜稳定性改变、微核和总畸形核生成,各种损伤均表现出明显的浓度依赖效应。2μg/L Hg暴露14天后,血细胞溶酶体膜中性红保持时间(NRR)、微核生成率(MN)和总畸形核生成率(TNA)与对照组相比没有显著差异。相同暴露时间下,25 μg/L Hg处理组血细胞NRR值低于25 μg/L Cd处理组,而MN和TNA值则相反,说明Hg胁迫对四角蛤蜊血细胞溶酶体膜具有较强的损伤作用。研究发现,NRR、MN和TNA三种指标对于衡量重金属污染对四角蛤蜊血细胞的毒性效应有很好的协同检测作用,可望作为有效的生物标志物在环境监测技术中得以应用。

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对虾病害在世界范围内肆虐,给水产养殖和沿海农村经济造成了重大损失。在水产养殖的实践中快速检测水产动物的病害并及时采取隔离等措施对于控制病害尤为重要,其中关键的环节就是快速检测出病害,并在对虾免疫机制上寻找对虾疾病防治的有效方法。研究表明当对虾等甲壳动物受到外界病原刺激时,极微量的微生物多糖就可以激活proPO系统。激活过程中涉及和产生一系列活性物质,如黑色素、酚氧化酶原激活因子(PPA)、模式识别蛋白(BGBP、PGBP、LGBP、LBP)及其膜上受体和A2巨球蛋白等,它们可通过多种方式参与防御反应,包括提供调理素,促进血细胞吞噬作用,形成结节或包囊以及介导凝集和凝固,产生杀菌物质并且黑色素化。黑色素常常在节肢动物的体表形成黑色斑点,形成的色素沉着对机体起到保护作用。所以,酚氧化酶原激活的级联反应是节肢动物免疫的关键因素。本论文研究开发了以环等温介导技术(LAMP)为基础的检测对虾白斑病毒(WSSV)和鳗弧菌(V. anguillarum)的快速检测方法。并从对虾对病害的免疫机制为切入点,从中国明对虾体内克隆了酚氧化酶原(PrpPO)和丝氨酸蛋白酶FcSP3这两个免疫系统中重要的基因,分析了它们的分子结构特征,组织分布及应答鳗弧菌病原刺激的表达变化模式。 建立的对虾常见病害对虾白班病毒(WSSV)和鳗弧菌(V. anguillarum)的LAMP检测方法,经过实验比对和Blast检索,发现本研究中使用的引物,比已经报导的LAMP方法或者PCR方法具有更宽的检测范围(更低的假阴性)。检测WSSV的LAMP方法使用病毒的VP28基因设计引物,而鳗弧菌的检测方法使用empA基因设计引物。在方法中,首次提出加入UNG酶和dUTP的措施来预防污染,在实际检测中非常有效。LAMP方法与PCR检测方法的灵敏性比较也进行了研究,二者灵敏性相当。 依据中国明对虾血液cDNA文库提供的部分片段信息,结合SMART-RACE技术,克隆了酚氧化酶原(PrpPO)基因,通过序列比对分析发现,PrpPO基因cDNA全长为3040 bp,其中开放阅读框2061 bp,编码686个氨基酸,其中推测的信号肽为12个氨基酸。推测的序列与斑节对虾(P. monodon)同源性为93%,与短钩对虾(P. semisulcatus.)同源性为92%。real time RT-PCR实验结果表明, ProPO在血细胞中的相对表达量最高,肝胰脏中表达量最低。弧菌刺激实验中注射弧菌,刺激了血细胞和淋巴器官中的ProPO mRNA显著增加,说明在血细胞和淋巴器官中存在快速反应的ProPO通路。而ProPO mRNA量在淋巴器官中在时间上早于血液中升至最高,说明该动物在在病原刚开始入侵的时候先有淋巴器官发挥主要的免疫作用,随着时间推移血细胞便变成主要的免疫器官。 根据中国明对虾肝胰脏cDNA文库提供EST信息,经过SMART-RACE克隆了一个丝氨酸蛋白酶FcSP3基因,通过序列比对分析发现,该丝氨酸蛋白酶基因cDNA全长为1622 bp,其中开放阅读框1431 bp,编码477个氨基酸,其中推测的信号肽为22个氨基酸。推测的序列与疟蚊的丝氨酸蛋白酶(A. gambiae)同源性为33%,与丽蝇蛹集金小蜂的酚氧化酶原激活因子(N. vitripennis)同源性为32%,与东北大黑鳃金龟的酚氧化酶原激活因子(H. diomphalia)同源性为34%。淋巴器官中PPAⅡ表达量约为血液中表达量的47560倍,肝胰脏中的FCSP3表达量为血细胞表达量的6226倍。鳗弧菌注射对虾后,淋巴器官中刺激组和对照组FcSP3的mRNA量在刺激后6小时显著降低,但是刺激组的表达量明显高于对照组。刺激组的血细胞与肝胰脏中FcSP3 mRNA的相对表达量增高。而病原刺激后的血液与肝胰脏中的FcSP3 mRNA的增长趋势也在时间上先与ProPO mRNA。这说明FcSP3对ProPO有正调控的作用,但这个调控有一个时间差,并且在不同组织中有不同的调控效率。

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自转基因作物问世以来,转基因产品的安全性问题一直是人们关注的焦点。本文根据GenBank中登录的转基因大豆完整外源DNA序列设计了几对引物,对转基因大豆进行了巢式PCR检测。结果表明,巢式PCR可以扩增10-10g/μl浓度的DNA溶液,检测灵敏度高达0.01%。该巢式PCR技术具有高度特异性、灵敏度和很好的重复性。用巢式PCR对部分市售的水产饲料和豆制食品进行检测,90.6%的水产饲料和46.5%的食品能检测出外源基因片段,表明转基因大豆广泛存在于水产饲料和我们的日常食品中,为食品安全分析和管理提供了方法和依据。环介导的等温扩增技术(LAMP)依赖于能够识别靶序列上6个特异区域的引物和一种具有链置换特性的DNA聚合酶,在等温条件下可高效、快速、高特异地扩增靶序列。本研究建立了转基因大豆的LAMP扩增技术,针对豆制品以及饲料的转基因LAMP检测技术正在研究和开发中。 利用转基因和非转基因豆粕制作的饲料,喂养吉富罗非鱼,分别于4周、7周取样,对其体重和血液指标进行了检测。实验显示,投喂转基因饲料7周以后,增重率和血清指标,转基因组与非转基因饲料组相比没有显著差异。全血指标中白细胞数目、大血小板比率、平均血小板体积和血小板体积分布宽度4项指标显著高于非转基因饲料组,而且差异达到极显著水平。由以上结果可见,转基因大豆与非转基因大豆相比,对罗非鱼的一些生理过程造成了一定的影响,但是并未对其生长造成可见的影响。分别于投喂1h、4h和8h以后取罗非鱼胃内容物、肠道内容物和粪便,并分别于4周、7周和继续饥饿2周后,取罗非鱼不同组织,提取DNA,用巢式PCR法检测转基因大豆中的外源基因在各种组织中的分布,结果显示在胃内容物、肠内容物、粪便、心脏、肝脏、胃、肠、卵巢、精巢、脑、鳃丝、脾脏、胆囊、肌肉等不同部位的DNA中都能检测到外源基因的存在,说明转基因大豆中的外源DNA并不能被罗非鱼的消化道完全降解,其DNA片段可能通过消化吸收转移到鱼体的各种组织。在投喂转基因饲料7周以后以及停止投喂饥饿2周以后分离水体中的微生物,提取其DNA,进行转基因检测。结果显示在所分离纯化的各种微生物中都没有检测到转基因大豆中外源基因35S-EPSPS的存在。

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Shrimps Litopenaeus vannamei with initial body weight of 2.108 +/- 0.036 g were sampled for specific growth rates (SGR) and body color measurements for 50 days under different light sources (incandescent lamp, IL; cool-white fluorescent lamp, FL; metal halide lamp, MHL; and control without lamp) and different illumination methods (illumination only in day, IOD, and illumination day and night, IDN). Body color of L. vannamei was measured according to the free astaxanthin concentration (FAC) of shrimp. The SGR, food intake (FI), feed conversion efficiency (FCE) and FAC of shrimps showed significant differences among the experimental treatment groups (P < 0.05). Maximum and minimum SGR occurred under IOD by MHL and IDN by FL, respectively (difference 56.34%). The FI of shrimp for the control group did not rank lowest among treatments, confirming that shrimp primarily use scent, not vision, to search for food. FI and FCE of shrimps were both the lowest among treatment groups under IDN by FL and growth was slow, thus FL is not a preferred light source for shrimp culture. Under IOD by MHL, shrimps had the highest FCE and the third highest FI among treatment groups ensuring rapid growth. FAC of shrimp were about 3.31 +/- 0.20 mg/kg. When under IOD by MHL and IDN by FL, FAC was significantly higher than the other treatments (P < 0.05). To summarize, when illuminated by MHL, L. vannamei had not only vivid body color due to high astaxanthin concentration but also rapid growth. Therefore, MHL is an appropriate indoor light source for shrimp super-intensive culture. SGR of shrimp was in significantly negative correlation to FAC of shrimp (P < 0.05). Thus, when FAC increased, SGR did not always follow, suggesting that the purpose of astaxanthin accumulation was not for growth promotion but for protection against intense light. (c) 2005 Elsevier B.V. All rights reserved.

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Using the LAMP method, a highly specific and sensitive detection system for genetically modified soybean (Roundup Ready) was designed. In this detection system, a set of four primers was designed by targeting the exogenous 35S epsps gene. Target DNA was amplified and visualized on agarose gel within 45 min under isothermal conditions at 65 degrees C. Without gel electrophoresis, the LAMP amplicon was visualized directly in the reaction tube by the addition of SYBR Green I for naked-eye inspection. The detection sensitivity of LAMP was 10-fold higher than the nested PCR established in our laboratory. Moreover, the LAMP method was much quicker, taking only 70 min, as compared with 300 min for nested PCR to complete the analysis of the GM soybean. Compared with traditional PCR approaches, the LAMP procedure is faster and more sensitive, and there is no need for a special PCR machine or electrophoresis equipment. Hence, this method can be a very useful tool for GMO detection and is particularly convenient for fast screening.

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In this work, a thiourea-modified chitosan derivative (TMCD) was synthesized through two steps, O-carboxymethylated first and then modified by a polymeric Schiff's base of thiourea/glutaraldehyde. The adsorption behavior of mercury (II) ions onto TMCD was investigated through batch method. The maximum adsorption capacity for Hg(II) was found to be 6.29 mmol/g at pH 5.0 and both kinetic and thermodynamic parameters of the adsorption process were obtained. The results indicated that adsorption process was spontaneous exothermic reaction and kinetically followed pseudo-second-order model. The adsorption experiments also demonstrated TMCD had high adsorption selectivity towards Hg(II) ions when coexisted with Cu(II), Zn(II), Cd(II) and Ca(II) in solution and it could be easily regenerated and efficiently reused. (C) 2010 Elsevier B.V. All rights reserved.

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A fast, sensitive and reliable potentiometric stripping analysis (PSA) is described for the selective detection of the marine pathogenic sulfate-reducing bacterium (SRB). Desulforibrio caledoiensis. The chemical and electrochemical parameters that exert influence on the deposition and stripping of lead ion, such as deposition potential, deposition time and pH value were carefully studied. The concentration of SRB was determined in acetate buffer solution (pH 5.2) under the optimized condition (deposition potential of -1.3 V. deposition time of 250 s, ionic strength of 0.2 mol L-1 and oxidant mercury (II) concentration of 40 mg L-1). A linear relationship between the stripping response and the logarithm of the bacterial concentration was observed in the range of 2.3 x 10 to 2.3 x 10(7) cfu mL(-1). In addition, the potentiometric stripping technique gave a distinct response to the SRB, but had no obvious response to Escherichia coli. The measurement system has a potential for further applications and provides a facile and sample method for detection of pathogenic bacteria. (C) 2010 Elsevier B.V. All rights reserved.