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Poliana Dutra Mai Laurence Maurice Emmanuel Tessier David Amouroux Daniel Coss Patricia Moreira-Turcq Henri Etcheber 《环境科学学报(英文版)》2018,30(6):24-40
Seasonal variability of dissolved and particulate methylmercury(F-MeHg, P-MeHg) concentrations was studied in the waters of the Amazon River and its associated Curuai floodplain during hydrological year 2005–2006, to understand the MeHg exchanges between these aquatic systems. In the oxic white water lakes, with neutral pH, high F-MeHg and P-MeHg concentrations were measured during the rising water stage(0.70 ± 0.37 pmol/L, n = 26) and flood peak(14.19 ± 9.32 pmol/g, n = 7) respectively, when the Amazon River water discharge into the lakes was at its maximum. The lowest mean values were reported during the dry season(0.18 ± 0.07 pmol/L F-MeHg, n = 10 and 1.35 ± 1.24 pmol/g P-MeHg, n = 8), when water and suspended sediments were outflowing from the lakes into the River. In these lakes,the MeHg concentrations were associated to the aluminium and organic carbon/nitrogen changes. In the black water lakes, with acidic pH and reducing conditions, elevated MeHg concentrations were recorded(0.58 ± 0.32 pmol/L F-MeHg, n = 16 and 19.82 ± 15.13 pmol/g PMeHg, n = 6), and correlated with the organic carbon and manganese concentrations. Elevated values of MeHg partition coefficient(4.87 Kd 5.08 log(L/kg) indicate that MeHg is mainly transported associated with the particulate phase. The P-MeHg enrichment detected in all lakes suggests autochthonous MeHg inputs from the sediments into the water column. The MeHg mass balance showed that the Curuai floodplain is not the source of P-MeHg for the Amazon River. 相似文献
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Chlorinated and polycyclic aromatic hydrocarbons in riverine and estuarine sediments from Pearl River Delta, China 总被引:53,自引:0,他引:53
Mai BX Fu JM Sheng GY Kang YH Lin Z Zhang G Min YS Zeng EY 《Environmental pollution (Barking, Essex : 1987)》2002,117(3):457-474
Spatial distribution of chlorinated hydrocarbons [chlorinated pesticides (CPs) and polychlorinated biphenyls (PCBs)] and polycyclic aromatic hydrocarbons (PAHs) was measured in riverine and estuarine sediment samples from Pearl River Delta, China, collected in 1997. Concentrations of CPs of the riverine sediment samples range from 12 to 158 ng/g, dry weight, while those of PCBs range from 11 to 486 ng/g. The CPs concentrations of the estuarine sediment samples are in the range 6-1658 ng/g, while concentrations of PCBs are in the range 10-339 ng/g. Total PAH concentration ranges from 1168 to 21,329 ng/g in the riverine sediment samples, whereas the PAH concentration ranges from 323 to 14,812 ng/g in the sediment samples of the Estuary. Sediment samples of the Zhujiang River and Macao harbor around the Estuary show the highest concentrations of CPs, PCBs, and PAHs. Possible factors affecting the distribution patterns are also discussed based on the usage history of the chemicals, hydrologic condition, and land erosion due to urbanization processes. The composition of PAHs is investigated and used to assess petrogenic, combustion and naturally derived PAHs of the sediment samples of the Pearl River Delta. In addition, the concentrations of a number of organic compounds of the Pearl River Delta samples indicate that sediments of the Zhujiang river and Macao harbor are most likely to pose biological impairment. 相似文献
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Increasing polybrominated diphenyl ether (PBDE) contamination in sediment cores from the inner Clyde Estuary,UK 总被引:1,自引:0,他引:1
Christopher H. Vane Yun-Juan Ma She-Jun Chen Bi-Xian Mai 《Environmental geochemistry and health》2010,32(1):13-21
The concentrations of 16 polybrominated diphenyl ether (PBDE) congeners in six short sediment cores from the Clyde Estuary
were determined by gas-chromatography mass-spectrometry. Total PBDE concentrations ranged from 1 to 2,645 μg/kg and the average
concentration was 287 μg/kg. BDE-209 was the main congener and varied from 1 to 2,337 μg/kg. Elevated total PBDE concentrations
were observed close to the sediment surface in the uppermost 10 cm of four of the six sediment cores. Comparison of the down
core PBDE profiles revealed that the increase was driven by the accumulation of deca-BDE. Although the deca-BDE mix was dominant,
the presence of lower molecular weight congeners BDE-47, BDE-99, BDE-183 and BDE-153 at most sediment intervals suggested
additional sources of penta-BDE and octa-BDE pollution. Changing PBDE source input was the major factor in influencing the
proportion of nona-brominated congeners, although other explanations such as post burial photo-debromination of BDE-209 cannot
be entirely discounted. A clear cascading to lower hepta-, hexa-, and penta-homologues was not found. The increase in total
PBDE concentrations and particularly the deca-BDE may possibly be ascribed to the use and subsequent disposal of electrical
appliances such as televisions and computers. In the Clyde sediments, the proportion of nona-brominated congeners was higher
than that reported for commercial mixtures. This might be due to changing sources of PBDEs or post burial photo-debromination
of BDE-209. 相似文献
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沉积物中多环芳烃和有机氯农药定量分析的质量保证和质量控制 总被引:118,自引:8,他引:118
以美国EPA为方法为基础,进行了沉积物中多环芳烃和有机氯农药分析的质量保证和质量控制实验,采用回收率指示物控制回收率,用内标法定量。结果表明多环芳烃的指示物回收率为50.67-97.33%,目标化合物的回收率为58.67-96.33%,方法检测限为3.30-9.26μg.kg^-1。 相似文献
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