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91.
有机氯类农药为已确定的环境雌激素,易在体内蓄积产生慢性毒性危害人体健康。选择单一存在时无明显雌激素效应的残留剂量进行联合试验,观察联合作用后雌激素效应的增减。选取乳腺癌MCF-7细胞作为研究对象,对残留剂量下六氯苯(HCB)、β-六六六(β-BHC)和p,p’-滴滴涕(p,p’-DDT)联合后的雌激素效应机制进行了研究。首先,运用MTT法观察3种有机氯类农药残留剂量下单独和联合作用对MCF-7细胞生长的影响;然后,运用流式细胞仪测定有机氯类农药联合对MCF-7细胞周期的影响;之后,采用Western Blot法测定有机氯类农药联合后ERα、ERβ、ERK1/2、p-ERK1/2、Ki67、c-Myc和Cyclin D1蛋白表达的变化。结果显示,β-BHC+p,p’-DDT组、HCB+β-BHC+p,p’-DDT组作用24 h后细胞增殖率为115.0%、120.1%,作用48 h后增殖率为121.2%、126.3%,其他联合组与对照相比未发生明显变化;β-BHC+p,p’-DDT组、HCB+β-BHC+p,p’-DDT组中MCF-7细胞的G1期细胞比例下降,S期细胞比例上升,细胞呈高增殖状态;β-BHC+p,p’-DDT组、HCB+β-BHC+p,p’-DDT组和雌二醇(E2)组作用48 h后,均降低ERα的蛋白表达,升高ERβ的蛋白表达,促进p-ERK1/2、Ki67、Cyclin D1和c-Myc的蛋白表达。研究表明,在单一作用时不具有雌激素效应的残留剂量下,仅β-BHC+p,p’-DDT联合组和HCB+β-BHC+p,p’-DDT联合组具有明显雌激素效应,其效应机制为经雌激素受体途径,激活ERβ蛋白表达,抑制ERα蛋白表达,促进p-ERK1/2、Ki67、c-Myc和Cyclin D1等相关蛋白的表达。  相似文献   
92.
为从物种雌激素受体(ERα)敏感性差异的角度探索辽东湾野生梭鱼雌雄同体高发生率的一个可能原因,从梭鱼肝脏cDNA中扩增出长1113 bp的梭鱼ERα(sERα) DEF区片段,并以此构建pGBT9-sERα DEF 质粒,将其和pGAD424-TIF2质粒依次转入Y190酵母细胞中,建立了sERα物种特异性的酵母双杂交筛选系统.在此系统中测试了4种环境中主要的雌激素雌酮(E1)、17β-雌二醇(E2)、雌三醇(E3)及17α-炔雌醇(EE2)对梭鱼ERα的诱导活性,半数雌激素活性浓度(EC50)为3.7、2.4、1698.7、1.2nmol/L,分别是青鳉鱼ERα活性的4.6、2.3、3.4、3.3倍,说明梭鱼ERα对E1、E2、E3、EE2具有较高的敏感性,这为解释辽东湾梭鱼雌雄同体的高发生现象提供了重要线索.  相似文献   
93.
应用重组基因酵母检测了天津市4个污水处理厂以及2个再生水厂13个水样的雌/孕激素干扰效应.其中3个污水处理厂的进水检出了雌激素诱导活性,最高检测值为10.7ngEEQ·L-1;所有水样均未检测出孕激素诱导活性,但都检测出不同程度的孕激素抑制活性,其中检出了雌激素诱导活性的污水处理厂的进水具有相对较强的孕激素抑制活性.4个污水处理厂均不能完全去除孕激素抑制活性物质,去除率在44%~78%之间.微滤和臭氧氧化两种工艺结合对孕激素抑制活性物质的去除效率略优于MBR反应器.2个再生水厂出水加氯后孕激素抑制活性均有所增强.  相似文献   
94.
为建立环境雌激素的体外快速筛选方法,采用免疫测定介导受体竞争结合试验定量检测环境雌激素.将17β-雌二醇-BSA固定在微孔板上,环境雌激素与微孔板上的17β-雌二醇-BSA竞争性地与雌激素受体结合,与微孔板上17β-雌二醇-BSA结合的受体与雌激素受体的抗体、雌激素受体抗体的二抗形成一个三明治形式的复合物,通过显色剂显色,最后用比色法对试验结果进行定量.结果表明,环境雌激素的浓度与溶液吸光度值成负相关.定量研究可以得到环境雌激素剂量-效应关系曲线,在一定浓度范围内(10ng·L-1~100μg·L-1),溶液的吸光度值与环境雌激素的浓度直接呈现良好的线性关系(R2=0.9583).利用这种方法能检测到的标准品雌二醇的最低浓度为10ng·L-1.以上结果表明,本方法检测环境雌激素操作简便,具有广泛的应用前景.  相似文献   
95.
Treatments of estrogens such as Estrone(E1), Estradiol(E2) and Ethinylestradiol(EE2) were conducted using an electrolytic reactor equipped with multi-packed granular glassy carbon electrodes.Experimental results showed that E1, E2 and EE2 were oxidized in the range of 0.45–0.85 V and were removed through electro-polymerization. Observed data from continuous experiments were in good agreement with calculated results by a mathematical model constructed based on mass transfer limitation. In continuous treatment of trace estrogens(1 μg/L), 98% of E1, E2 and EE2 were stably removed. At high loading rate(100 μg/L), removal efficiency of E1 was kept around 74%–88% for21 days, but removal efficiency reduced due to passivation of electrodes. However, removal efficiency was recovered after electrochemical regeneration of electrodes in presence of ozone. Electric energy consumption was observed in the range of 1–2 Wh/m3. From these results, we concluded that the present electrochemical process would be an alternative removal of estrogens.  相似文献   
96.
Goals, Scope and Background Fish populations, especially those of the grayling (Thymallus thymallus), have declined over the last two decades in the upper Danube River between Sigmaringen and Ulm, despite intensive and continuous stocking and improvement of water quality since the 1970s. Similar problems have been reported for other rivers, e.g. in Switzerland, Great Britain, the United States and Canada. In order to assess if ecotoxicological effects might be related to the decline in fish catch at the upper Danube River, sediment, suspended matter and waste water samples from sewage treatment plants were collected at selected locations and analyzed in a bioanalytical approach using a battery of bioassays. The results of this pilot study will be used to decide if a comprehensive weight-of-evidence study is needed. Methods Freeze-dried sediments and suspended particulate matters were extracted with acetone in a Soxhlet apparatus. Organic pollutants from sewage water were concentrated using XAD-resins. In order to investigate the ecotoxicological burden, the following bioassays were used: (1) neutral red assay with RTL-W1 cells (cytotoxicity), (2) comet assay with RTLW1 cells (genotoxicity), (3) Arthrobacter globiformis dehydrogenase assay (toxicity to bacteria), (4) yeast estrogen screen assay (endocrine disruption), (5) fish egg assay with the zebrafish (Danio rerio; embryo toxicity) and (6) Ames test with TA98 (mutagenicity). Results and Discussion The results of the in vitro tests elucidated a considerable genotoxic, cytotoxic, mutagenic, bacteriotoxic, embryotoxic and estrogenic burden in the upper Danube River, although with a very inhomogeneous distribution of effects. The samples taken from Riedlingen, for example, induced low embryo toxicity, but the second highest 17β-estradiol equivalent concentration (1.8 ng/L). Using the fish egg assay with native sediments, a broad range of embryotoxic effects could be elucidated, with clear-cut dose-response relationships for the embryotoxic effects of contaminated sediments. With native sediments, embryotoxicity was clearly higher than with corresponding pore waters, thus corroborating the view that – at least for fish eggs – the bioavailability of particle-bound lipophilic substances in native sediments is higher than generally assumed. The effect observed most frequently in the fish egg assay was a developmental delay. A comparison of our own results with locations along the rivers Rhine and Neckar demonstrated similar or even higher ranges of ecotoxicological burdens in the Danube River. Conclusions The complex pattern of ecotoxicological effects caused by environmental samples from the Danube River, when assessed in an in vitro biotest battery using both acute and more specific endpoints, showed that integration of different endpoints is essential for appropriate hazard assessment. Overall, the ecotoxicological hazard potential shown has indeed to be considered as one potential reason for the decline in fish catches at the upper Danube River. However, based on the results of this pilot study, it is not possible to elucidate that chemically induced alterations are responsible for the fish decline. Recommendations and Perspective . In order to confirm the ecological relevance of the in vitro results for the situation in the field and especially for the decline of the grayling and other fishes, further integrated investigations are required. For linking the weight of evidence obtained by in vitro assays and fish population investigations, the application of additional, more specific biomarkers (e.g. vitellogenin induction, EROD and micronucleus assay) has been initiated in fish taken from the field as well as in situ investigations.  相似文献   
97.
为了探讨蛋白质组学技术在环境雌激素分析上的应用,用浓度为3.7×10-9mol/L的17β-雌二醇(E2)处理MCF-7细胞2或3天后进行双向电泳,对比不同的蛋白质提取、染色方法,利用光密度扫描仪将电泳图像数字化,并使用PDQuest软件进行图像分析,以观察雌激素诱导下的蛋白质表达图谱。结果表明,在蛋白质的提取上,冻融法比超声裂解法更有效;在蛋白质染色上,银染法比考马斯亮蓝染色法能得到更多可显示的蛋白质斑点。用E2处理72h后的MCF-7细胞,可检测到40个下调蛋白和5个上调蛋白。该蛋白质表达模式的改变提示了环境雌激素诱导下的特异性蛋白质表达图谱变化。本研究为分析雌激素类内分泌干扰物的内在作用机制提供了一种新的可行方法,也为建立其高通量筛选方法提供了新的思路。  相似文献   
98.
DEHP、DBP内分泌干扰活性的实验研究   总被引:8,自引:1,他引:8       下载免费PDF全文
利用MCF-7细胞增殖实验、细胞周期分析、细胞雌激素受体水平测定和断乳大鼠子宫增重实验探讨了邻苯二甲酸二乙基己酯(DEHP)和邻苯二甲酸二丁酯(DBP)内分泌干扰活性及其可能的作用机制.结果表明,DEHP和DBP可诱导MCF-7细胞增殖、细胞内雌激素受体水平增高,对细胞周期无明显影响,DEHP不引起断乳大鼠子宫增重.推断DEHP和DBP可能并不是通过模拟雌激素而是引起体内天然激素受体水平改变等其他机制影响机体内分泌系统.  相似文献   
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