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191.
赤潮发生时产生的一些海洋生物毒素对人类和海洋动物的安全形成潜在的威胁甚至导致死亡.为从分子水平探讨鱼类中海洋藻毒素的去毒分子机理,采用RT-PCR法克隆了真鲷(Pagrus major)肝脏芳香烃受体核转位蛋白(ARNT)和I时相异生素代谢酶细胞色素P4501A(CYP1A)基因cDNA核心序列,同时,应用半定量RT-PCR方法,以β-肌动蛋白作为外参照,在其指数期增长的范围内研究了芳香烃受体(AHR)、ARNT、CYP1A、II时相异生素代谢酶alpha型谷胱甘肽S-转移酶(GSTA1、GSTA2)、rho型谷胱甘肽S-转移酶(GSTR)、热休克蛋白70(HSP70)基因组成型表达水平.结果发现,真鲷ARNT、CYP1A基因cDNA核心序列片段分别长438bp和908bp,分别编码146和302个氨基酸.序列同源性分析发现,真鲷与门齿鲷(Stenotomus chrysops)、石首鱼(Micropogon undulatus)ARNT基因氨基酸序列同源性高达97.2%、95.2%,与斑马鱼(Brachydanio rerio)、人、大鼠、小鼠ARNT同源性较低(77.2%~79.3%).真鲷与门齿鲷、金头鲷(Sparus auratus)、欧洲川鲽(Rhombus maximus)、欧洲海鲈(Dicentrachus labrax)CYP1A基因氨基酸序列同源性较高,为84.8%~94.0%,与斑马鱼、人、小鼠CYP1A同源性较低,为59.6%~77.8%.真鲷肝脏AHR、ARNT、CYP1A、GSTA1、GSTA2、GSTR和HSP70基因组成型表达水平分别为(25.32±6.56)%、(26.22±4.24)%、(146.5±16.06)%、(55.42±3.75)%、(48.82±10.89)%、(79.47±3.13)%、(107.42±14.34)%.  相似文献   
192.
为了研究自然水体中产毒藻细胞和微囊藻毒素(MC)的迁移转化机理,以经济实用的木炭为填料的柱状反应器对含微囊藻和MC的自然水进行了分阶段连续性去除实验。结果表明,当进水叶绿素a(chl-a)浓度为94.9~203.4 μg/L,MC浓度为4.5~24.7 μg/L时,藻细胞(以chl-a浓度为指标) 的去除率高于77.1%,MC的去除率高于66.2%。不同阶段的结果比较发现,HRT为6.8 h时去除效果最佳。反应器中,原生动物和后生动物大量存在,以钟型虫(Vorticella sp.)、草履虫(Paramecrum sp.)、旋轮虫(Philodina sp.)和腔轮虫(Lecane sp.)为主要物种。实时荧光定量PCR分析结果表明,可降解MC细菌的特异性基因(mlrA)被检出。由此说明,除木炭填料的物理吸附外,微型浮游动物的捕食及细菌降解对水中藻细胞和MC的去除也起重要作用。  相似文献   
193.
利用PCR方法从解淀粉芽孢杆菌DC 4总DNA中扩增出豆豉溶栓酶 (DFE)成熟肽编码区片段 .测序结果表明 :DFE成熟肽编码区长 82 5bp,编码 2 75个氨基酸残基 ,分子量为 2 7.7× 10 3 ,推导的N’ -端氨基酸序列与豆豉溶栓酶N’ -端氨基酸测序结果完全一致 ,说明克隆到的基因确实是豆豉溶栓酶基因 .同源性分析表明 ,DFE成熟肽编码区的核苷酸和氨基酸序列与日本纳豆激酶的同源性分别为 80 .0 %和 86 .5 % ,这提示豆豉溶栓酶可能是一种新型的溶栓酶 .将表达质粒pET Nde转化E .coliBL2 1(DE3)中 ,IPTG可诱导表达大量的DFE融合蛋白 ,占菌体可溶性蛋白的 4 0 % ,主要以包涵体的形式存在 .图 3表 1参 19  相似文献   
194.
195.
为探究污水处理厂生物气溶胶抗生素抗性基因(ARGs)污染特征,在济南市某污水处理厂采用宏基因组测序技术对厂界内及周边生物气溶胶样本及污水或污泥样本进行分析.结果表明,相比于上风向,厂界内和下风向生物气溶胶具有更多的ARGs亚型种类数和更高的总相对丰度.厂界内与上风向生物气溶胶ARGs组成存在显著的差异性,差异度为47.57%;而厂界内与下风向生物气溶胶ARGs组成的差异性不显著,且差异度下降至33.98%.上风向背景空气和污水或污泥均是厂界内生物气溶胶ARGs的重要来源,两者总的源的贡献大于63.92%.共检测到43种ARGs亚型(8种ARGs主型)在至少一处污水处理单元极易负载于生物气溶胶颗粒逸出.本研究可为污水处理厂生物气溶胶抗生素抗性污染的风险评估和控制提供理论依据.  相似文献   
196.
197.
We present the first confirmed case by molecular analysis of a metaphyseal chondrodysplasia, McKusick type, in a 22-week fetus. Two novel compound heterozygous mutations, 64T> A and 79G > T, were found in the highly conserved regions of the RMRP gene. Twenty-two heterozygous g.1018 T> C mutations, two homozygous g.1018 T> C mutations, two heterozygous insertion mutations g.799_g.800insC and one heterozygous insertion mutation g.849_g.850insT were found among 100 normal controls. Careful radiological examination of the fetus for skeletal dysplasia allowed definitive diagnosis, proper genetic counselling and future prenatal diagnosis. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   
198.
Abstract:  It has been suggested that transgenics and vertebrate cloning have a role to play in conservation. Now is the time to evaluate their risks and benefits, before these technologies are widely implemented in our field. Direct risks of transgenics include escape and introgression of transgenes into wild populations; weedy invasion by transgenic organisms; toxicity or pathogenicity of engineered organisms and their products; and human error in the field testing and tracking of transgenic organisms. Indirect risks include environmental effects of increased herbicide use; the danger that engineered organisms may aid the development of bioweapons; the likelihood that gene patenting will lead to the privatization of natural resources; and the diversion of support from less glamorous forms of conservation. Formal risk assessments are commonly used to evaluate transgenic procedures, but our incomplete understanding of both ecosystem processes and the action of transgenes renders most of these assessments scientifically and socially unjustified. Nevertheless, a few, low-risk applications of transgenics may be possible: for example, "super-sterile" ornamental cultivars. Vertebrate cloning poses little risk to the environment, but it can consume scarce conservation resources, and its chances of success in preserving species seem poor. To date, the conservation benefits of transgenics and vertebrate cloning remain entirely theoretical, but many of the risks are known and documented. Conservation biologists should devote their research and energies to the established methods of conservation, none of which require transgenics or vertebrate cloning.  相似文献   
199.
Zoige wetland is one of the most important methane emission centers in China. The oxidation of methane in the wetland a ects global warming, soil ecology and atmospheric chemistry. Despite their global significance, microorganisms that consume methane in Zoige wetland remain poorly characterized. In this study, we investigated methanotrophs diversity in soil samples from both anaerobic site and aerobic site in Zoige wetland using pmoA gene as a molecular marker. The cloning library was constructed according to the pmoA sequences detected. Four clusters of methanotrophs were detected. The phylogenetic tree showed that all four clusters detected were a liated to type I methanotrophs. Two novel clusters (cluster 1, cluster 2) were found to relate to none of the recognized genera of methanotrophs. These clusters have no cultured representatives and reveal an ecological adaptation of particular uncultured methanotrophs in Zoige wetland. Two clusters were belonging to Methylobacter and Methylococcus separately. Denaturing gradient gel electrophoresis gel bands pattern retrieved from these two samples revealed that the community compositions of anaerobic soil and aerobic soil were di erent from each other while anaerobic soil showed a higher metanotrophs diversity. Real-time PCR assays of the two samples demonstrated that aerobic soil sample in Zoige wetland was 1.5 times as much copy numbers as anaerobic soil. These data illustrated that methanotrophs are a group of microorganisms influence the methane consumption in Zoige wetland.  相似文献   
200.
A water bloom sample collected from Lake Dishui in Shanghai was characterized.The morphological identification showed that Micorcystis wesenbergii and Micorcystis smithii were the main component of the bloom.Five strains of M.smithii were successfully isolated.Their 16S rRNA gene sequences based phylogenetic tree showed that the five strains of M.smithii intermixed with strains of other morphospecies in Microcystis.A fragment of mcy gene encoding for microcystin synthetase was detected in one of the five M....  相似文献   
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