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881.
River waters in China have dual contamination by nutrients and recalcitrant organic compounds. In principle, the organic compounds could be used to drive denitrification of nitrate, thus arresting eutrophication potential, if the recalcitrant organics could be made bioavailable. This study investigated the potential to make the recalcitrant organics bioavailable through photocatalysis. Batch denitrification tests in a biofilm reactor demonstrated that dual-contaminated river water was short of available electron donor, which resulted in low total nitrogen (TN) removal by denitrification. However, the denitrification rate was increased significantly by adding glucose or by making the organic matters of the river water more bioavailable through photocatalysis. Photocatalysis for 15 min increased the Chemical Oxygen Demand (COD) of the river water from 53 to 84 mg·L-1 and led to a 4-fold increase in TN removal. The increase in TN removal gave the same effect as adding 92 mg·L-1 of glucose. During the photocatalysis experiments, the COD increased because photocatalysis transformed organic molecules from those that are resistant to dichromate oxidation in the COD test to those that can be oxidized by dichromate. This phenomenon was verified by testing photocatalysis of pyridine added to the river water. These findings point to the potential for N removal via denitrification after photocatalysis, and they also suggest that the rivers in China may be far more polluted than indicated by COD assays.  相似文献   
882.
研究了广州及周边地区5处代表性森林土壤(鼎湖山、西樵山、华南植物园、黄埔和南昆山)As、Se、Hg质量分数特征及污染状况。结果表明,上述5地森林表层土壤As质量分数平均值分别为18.6、18.0、12.2、11.4、26.1 mg.kg-1,Se质量分数平均值分别为0.360、0.729、0.286、0.421、0.434 mg.kg-1,Hg质量分数平均值分别为0.201、0.270、0.139、0.224、0.087 mg.kg-1。除植物园土壤Se质量分数、南昆山土壤Hg质量分数较接近背景值外,5林地As、Se、Hg质量分数均超过背景值,可能存在外源As、Se、Hg输入。其中,南昆山As输入,西樵山Se、Hg输入,黄埔、鼎湖山Hg输入较明显。单因子污染指数分析结果表明在南昆山As为最严重的污染物,而在鼎湖山、植物园、西樵山和黄埔Hg为最严重的污染物。综合污染指数分析结果表明5林地土壤均受到不同程度的污染,其中西樵山土壤属重度污染,南昆山、黄埔、鼎湖山属中度污染,植物园污染较轻,属轻度污染。  相似文献   
883.
Soil samples from 4 defined city zones of Nanjing were randomly collected at 0-5 cm and 5-20 cm intervals and size fractions of soil particles were separated from undisturbed bulk soils by low energy dispersion procedure. The total contents of Cu and Pb in the different particle size fractions of the urban soils were analyzed by HNO3-HF-HClO4 digestion and flame atomic absorption spectrophotometer determination. The total content of Cu and Pb in soil particle size fractions varied with their size and with city zones as well. Both the content and variation with the size fractions of Pb was bigger than of Cu supporting our previous finding that there was Pb pollution to different degrees in the urban soils although the two elements were generally enriched in clay-sized fraction. Contaminated Pb tended to be preferentially enriched in the size fraction of 2000-250 μm and clay-sized fraction. While the size fractions of the soils from newly developed and preserved area contained smaller amount of Cu and Pb, the partitioning of them in coarse and fine particle size fractions were insignificant compared to that from inner residence and commercial area. The very high Pb level over 150 mg/kg of the fine particle fractions from the soils of the inner city could be a cause of high blood Pb level reported of children from the city as acute exposure to Pb of fine particles of the urban soil might occur by soil ingestion and inhalation by young children. Thus, much attention should be paid to the partitioning of toxic metals in fine soil particles of the urban soils and countermeasures against high health risk of Pb exposure by soil ingestion and dust inhalation should be practiced against the health problem of blood Pb for young children from the cities.  相似文献   
884.
Gaobeidian Lake, located in Beijing, China, serves as a recipient lake for e uents from a large municipal sewage treatment plant (MSTP). In order to evaluate the e ects of discharging MSTP e uent on the mercury contamination of the local aquatic ecosystem, sediment cores, water, plankton, fish, and turtle samples were collected from Gaobeidian Lake for mercury speciation analysis. High concentrations of total mercury (T-Hg) were detected in sediment cores (5.24–17.0 g/g dry weight (dw), average: 10.1 g/g). The ratio of methylmercury (MeHg) to T-Hg was less than 0.3% in sediments and ranged from 35% to 76% in biota samples. The highest level of T-Hg and MeHg were found in aquatic bryophyte and crucian carp (3673 and 437 ng/g dw, respectively). The relative contents of MeHg were significantly correlated with trophic levels (R2 = 0.5506, p < 0.001), which confirmed that MeHg can be bio-transferred and biomagnified via food chain in this aquatic ecosystem.  相似文献   
885.
三峡水库入库支流水体中营养盐季节变化及输出   总被引:12,自引:10,他引:12  
三峡水库成库后,对三峡水库13条主要支流入库断面有机物、营养盐、生物量含量季节变化进行了初步研究.结果表明,支流高锰酸盐指数、化学需氧量(COD)、总氮(TN)、氨氮(NH+4-N)、总磷(TP)、叶绿素a(Chl-a)含量季节间差异较大.高锰酸盐指数范围为0.20~5.91 mg·L-1,COD含量范围4.06~30.2 mg·L-1,TN含量范围为0.542~7.44 mg·L-1,NH+4-N含量范围0.034~2.83 mg·L-1,TP含量范围为0.010~0.449 mg·L-1,Chl-a值范围为1.02~128 mg·m-3.支流受到不同程度污染,水体中N含量丰富,部分支流富营养化的限制因子为P.除苎溪河外,其余支流Chl-a含量较低,仅为贫-中营养水平.双因子方差分析表明,营养因子在时间、空间分布上均有不同程度差异.利用相关分析方法,分析了叶绿素a与营养盐之间的关系,叶绿素a与有机物、营养盐都呈显著正相关关系.支流营养盐、有机物输出负荷主要受流量控制,表现为丰水期>平水期>枯水期. 13条支流不同季节排放COD、高锰酸盐指数、NH+4-N、TN和TP范围分别为1 772~6 701、 380~1 875、 40.1~172、 249~922和9.97~50.5 g·s-1.三峡水库支流有机物、营养盐的排放应引起关注.  相似文献   
886.
土壤重金属污染的调控机理及应用研究   总被引:1,自引:1,他引:1  
土壤重金属物污染的调控机理和应用研究,是国内外重金属污染土壤修复技术研究的热点和前沿领域。通过利用生物作用、理化措施等调控技术,可降低土壤中重金属的有效态浓度,降低其生物有效性及迁移性。文章阐述了利用植物、微生物、化学改良剂等修复土壤重金属污染的调控机理、影响因素、应用技术等方面的研究现状,讨论了植物修复、微生物作用、固定沉淀、吸附络合、有机络合及螯合、离子拮抗等原理与措施,并提出了其研究应用的发展趋势和展望。  相似文献   
887.
塌陷地粉煤灰充填复垦土壤的污染性分析   总被引:28,自引:0,他引:28       下载免费PDF全文
从粉煤灰的污染潜势分析入手,通过复垦土壤的测试分析、淋溶试验和种植试验,揭示了粉煤灰充填复垦土壤的污染性.研究表明,粉煤灰中重金属的水溶性差,同时因pH值高,抑制了作物对高含量污染重金属的吸收;淋溶试验也表明重金属元素的淋溶性弱;温室盆栽与大田作物籽实样品分析表明,样品中重金属含量符合国家有关标准,说明尽管复垦土壤存在重金属污染,仍然可以种植某些作物.  相似文献   
888.
含铁材料对污染水稻土中砷的稳定化效果   总被引:9,自引:0,他引:9  
通过化学实验方法,向砷污染水稻土中添加4种含铁材料(FeCl3、FeCl2、Fe0和Fe2O3),分析稳定后土壤中pH、砷形态及砷毒性浸出量的变化,研究4种含铁材料对污染水稻土中砷的稳定化效果。结果表明,FeCl3和FeCl2处理降低了土壤pH,Fe0和Fe2O3处理对土壤pH影响不大。4种含铁材料均明显降低了土壤中易溶态砷(WE-As)和毒性浸出砷含量。在最大添加量为8.00 g/kg时,FeCl3、FeCl2、Fe0和Fe2O3分别使易溶态砷比对照降低了86.4%、63.6%、77.3%和36.4%,使毒性浸出砷比对照降低了96.3%、88.9%、70.4%和30.4%。4种含铁材料均对水稻土壤中砷具有较好的稳定化效果,且能力大小依次为:FeCl3FeCl2、Fe0Fe2O3。Fe0和Fe2O3处理使WE-As、铝型砷(Al-As)、铁型砷(Fe-As)向钙型砷(Ca-As)和残渣态砷(RS-As)转化;FeCl3处理使土壤WE-As、Al-As向Fe-As、Ca-As和RS-As转化;FeCl2处理使土壤WE-As、Ca-As向Al-As、Fe-As转化,对RS-As影响不明显。说明Fe0固砷的机理与Fe2O3相似,与FeCl3有一定差异,与FeCl2的差异可能更大。  相似文献   
889.
Molecular approaches to microbiological monitoring: fecal source detection   总被引:1,自引:0,他引:1  
Molecular methods are useful both to monitor natural communities of bacteria, and to track specific bacterial markers in complex environments. Length-heterogeneity polymerase chain reaction (LH-PCR) and terminal restriction fragment length polymorphism (T-RFLP) of 16S rDNAs discriminate among 16S rRNA genes based on length polymorphisms of their PCR products. With these methods, we developed an alternative indicator that distinguishes the source of fecal pollution in water. We amplify 16S rRNA gene fragments from the fecal anaerobic genus Bacteroides with specific primers. Because Bacteroides normally resides in gut habitats, its presence in water indicates fecal pollution. Molecular detection circumvents the complexities of growing anaerobic bacteria. We identified Bacteroides LH-PCR and T-RFLP ribosomal DNA markers unique to either ruminant or human feces. The same unique fecal markers were recovered from polluted natural waters. We cloned and sequenced the unique markers; marker sequences were used to design specific PCR primers that reliably distinguish human from ruminant sources of fecal contamination. Primers for more species are under development. This approach is more sensitive than fecal coliform assays, is comparable in complexity to standard food safety and public health diagnostic tests, and lends itself to automation and high-throughput. Thus molecular genetic markers for fecal anaerobic bacteria hold promise for monitoring bacterial pollution and water quality.  相似文献   
890.
苟体忠  阮运飞 《化工环保》2012,40(3):336-341
以万山汞矿区土壤为研究对象,采用电感耦合等离子体质谱仪和原子荧光光谱仪测定土壤中的重金属含量,分别运用内梅罗综合污染指数(NPI)法和潜在生态风险指数(RI)法评价土壤重金属污染和潜在生态风险,并应用相关性分析、主成分分析和聚类分析对土壤重金属来源进行分析。结果表明:土壤Hg、Cd、As、Pb、Cu、Ni和Zn出现不同程度累积,分别达贵州省背景值的263.61、2.31、1.28、2.11、1.70、1.01和3.52倍;土壤重金属平均NPI为188.00,属于严重污染水平,Hg是主要污染因子;土壤重金属平均RI为10 655.70,属于极强潜在生态风险水平,Hg是主要潜在生态风险因子;土壤中Cu、Ni、Cr主要源于自然活动,As、Pb、Zn主要源于燃煤和交通运输污染,Cd主要源于农业污染,Hg主要源于汞冶炼污染。  相似文献   
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