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131.
Xu Y Zhang G Li J Chakraborty P Li H Liu X 《Journal of environmental monitoring : JEM》2011,13(11):3119-3127
A range of organochlorinated compounds have been consumed in China, India and the countries of mainland southeast Asia (MSA). Considering their persistence in the environment and ability in long-range atmospheric transport (LRAT), the potential outflow of these compounds from this region is therefore of great concern in the context of the global distribution of toxic chemicals. As part of a monitoring campaign aimed at investigating the LRAT of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) from southern China, MSA and northern India, atmospheric levels of OCPs and PCBs were measured once a week from October 2005 through December 2006 at Tengchong Mountain (TM), a remote site located in south-western China. The average concentrations of OCPs were found to be higher than those in other remote stations in the Arctic and the Tibetan plateau, except for α-hexachlorocyclohexane (α-HCH). A high level of β-HCH and low α-HCH/β-HCH ratio was attributed to an accidental release of β-HCH from unknown sources, besides obvious evidence of lindane (γ-HCH) and technical HCH usage. Temporal variations of chlordanes and endosulfan were related to the usage pattern of these compounds, as well as LRAT. In contrast, dichlorodiphenyltrichloroethane (DDT) exhibited a relatively minor seasonal variation. The OCP levels at the monitoring site were found to be related to the air parcel back trajectories on the basis of four distinct clusters. Elevated levels of HCHs and DDTs were observed when air parcels originated from northern India where considerable OCP usage was reported recently, while high levels of γ-HCH and TC (trans-chlordane) were mainly associated with air masses from southern China and northern MSA. The study highlighted the high background level of OCPs as well as their temporal patterns of trans-boundary LRAT in the MSA region. 相似文献
132.
Pan X Tang J Li J Zhong G Chen Y Zhang G 《Journal of environmental monitoring : JEM》2011,13(4):886-893
62 riverine and marine sediments were collected from the Laizhou Bay area, where the largest manufacturing base of brominated flame retardants (BFRs) in Asia is located. Eight polybrominated diphenyl ethers (PBDEs) were analyzed to investigate the impact of rapidly-developed bromine industries on the regional aquatic system. PBDE concentrations varied largely in riverine sediments. Σ(7)PBDEs (including BDE 28, 47, 99, 100, 153, 154 and 183) and BDE 209 ranged from 0.01 to 53 ng g(-1) dw and from 0.74 to 285 ng g(-1) dw with a mean value of 4.5 ng g(-1) dw and 54 ng g(-1) dw, respectively, indicating a strong influence of direct pollution discharges from local factories. In marine sediments, Σ(7)PBDEs and BDE 209 ranged from not detected (nd) to 0.66 ng g(-1) dw and from 0.66 to 12 ng g(-1) dw with a mean value of 0.32 ng g(-1) dw and 5.1 ng g(-1) dw, respectively. PBDE concentrations were mostly <10 ng g(-1) dw for Σ(7)PBDEs and <50 ng g(-1) dw for BDE 209, which are at a relatively low level for monitored riverine and coastal sediments around the world. Even at the most contaminated sites in Laizhou Bay area, PBDE concentrations were not among the highest concentrations reported in the literature. Congener compositions were dominated by BDE 209 (57.2-99.9% of the sum of BDE congeners), with minor contributions from penta- and octa-BDE products. Tri- to octa-BDE congeners were well correlated among each other (r > 0.75) and thus sources from similar mixing of penta- and octa-BDE products were suggested in this area. Compared with riverine sediments, a much better correlation between PBDE concentrations with TOC was observed in marine environment. The congener pattern changed and their correlation coefficients among each other were remarkably reduced. Contributions of BDE 28, 47 and 99 to Σ(7)PBDEs were generally the same in almost all the marine sites, while it was distinctively higher for BDE 153. These are probably attributable to several reasons, such as contributions by atmospheric deposition and/or redistribution between particles of various sizes during and/or after fluvial transportation combined with the difference of physiochemical properties of BDE congeners. 相似文献
133.
134.
Zhang Tongsheng & Gan Guohui Institute of Geographical Sciences Natural Resources Research Chinese Academy of Sciences Beijing China Graduate School Chinese Academy of Sciences Beijing China 《中国人口.资源与环境(英文版)》2006,4(1)
This paper empirically examines variations and changes in manufacturing concentration and their determinants in China over the 1980-2003 period with a sample of 26 industries. The analysis indicates that average industrial concentration has increased during the 1990s. Studies show that scale economies and industry policies are important determinants for industries geographical concentration; factor endowments and the location of foreign direct investment are also found to have a positive effect on concentration. 相似文献
135.
136.
利用1954~2008年街阳8个地面气象观测站数据,对其年代际间曲线和气侯趋势系数进行综合分析,结果表明:衡阳冰冻的年代际间变化经历了上世纪70年代的活跃期,50、90年代的低谷期,目前向正常方向发展.年平均出现冰冻24.5站次,冰冻多发年的出现机率有所加大,但仍处于较低水平.1月中旬~2月上旬是冰冻相对集中时段,其中1月下旬是全年出现冰冻最多旬,而该旬并非气温最低时段.形成冰冻的有利条件是日平均气温0~-1℃,小~中等降雨(雪)过程,日平均风速5.0 m/s以下.衡阳的冰冻发生存在地域性特点,自北向南逐渐减少.轻度冰冻、中等冰冻和重度冰冻各占69.3%、25.4%和5.3%. 相似文献
137.
珠江口及南海近海海域大气多环芳烃分布特征 总被引:3,自引:0,他引:3
分冬、春两次航次分别采集了珠江口及南海近海海域大气气溶胶样品和气相样品,同时以广州和中山作为陆基对照点,对16种EPA优控多环芳烃进行了分析.结果表明,大气PAHs主要以气态化合物为主,总PAHs(气态+颗粒态)的含量范围为49.6~256.6 ng/m3,平均120.7 ng/m3.珠江口海域大气颗粒态多环芳烃季节变化显著,冬、春航次大气颗粒态多环芳烃的含量分别为6.7~18.0 ng/m3和0.4~5.1 ng/m3,冬季航次期间大气颗粒态PAHs含量的高值主要源于大陆气流对城市群大气PAHs污染的输送,另外干冷的季节亦有利于PAHs向颗粒态的富集.与此相反,气态多环芳烃含量的季节差异不明显.在冬季,随东北季风携带的城市粉尘可以将大气中的气态PAHs捕获,而春季航次的大气PAHs主要来源于西太平洋地区的远程输送和PAHs的海-气交换作用.认为受控于季风活动的水、热因子组合特征,是影响珠江口海域大气PAHs含量与分布的主导因素. 相似文献
138.
利用1954-2008年衡阳8个地面气象观测站数据,对其年代际问曲线和气候趋势系数进行综合分析,结果表明-衡阳冰冻的年代际间变化经历了上世纪70年代的活跃期,50、90年代的低谷期,目前向正常方向发展。年平均出现冰冻24.5站次,冰冻多发年的出现机率有所加大,但仍处于较低水平。1月中旬-2月上旬是冰冻相对集中时段,其中1月下旬是全年出现冰冻最多旬,而该旬并非气温最低时段。形成冰冻的有利条件是日平均气温0— -1℃,小-中等降雨(雪)过程,日平均风速5.0m/s以下。衡阳的冰冻发生存在地域性特点,自北向南逐渐减少。轻度冰冻、中等冰冻和重度冰冻各占69.3%、25.4%和5.3%。 相似文献
139.
The experimental study on ozonation of ethylenethiourea(ETU) is conducted.The reaction of gas-phase ETU with 0.63 × 10-6 mol/L ozone is carried out in a 200-L reaction chamber.The secondary organic aerosol(SOA) resulted from the ozonation of gas-phase ETU is observed with a scanning mobility particle size(SMPS).The rapid exponential growth of SOA reveals that the atmospheric lifetime of ETU vapor towards ozone reaction is less than four days.The ozonation of dry ETU particles,ETU-contained water droplets an... 相似文献
140.