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61.
本文从价格视角将我国稀土市场结构的变化历程划分为不同阶段,分别从理论和现实视角上探讨了在国际、国内都是完全竞争市场,国际市场垄断、国内市场完全竞争,国际市场完全竞争、国内市场垄断,国际、国内都是垄断市场条件下稀土最优开采路径及最优耗竭时间,并通过设定参数判断其相对大小关系。发现在一定的假设条件下,开采前期当国内和国际市场都是完全竞争时,稀土最优开采量是最大的;当国内和国际市场都是垄断时,稀土最优开采量是最小的;其他两种市场情况下稀土最优开采量居于中间,当国际市场是稀土的主要消费地时,国际竞争-国内垄断市场情况下稀土最优开采量大于国际垄断-国内竞争市场情况下稀土最优开采量,反之,国际垄断-国内竞争市场情况下稀土最优开采量大于国际竞争-国内垄断市场情况下稀土最优开采量。 相似文献
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Johannes Kobler Walter J. Fitz Michael Mirtl 《Environmental pollution (Barking, Essex : 1987)》2010,158(3):849-854
Anthropogenic trace element emissions have declined. However, top soils all over the world remain enriched in trace elements. We investigated Pb and Cd migration in forest soils of a remote monitoring site in the Austrian limestone Alps between 1992 and 2004. Large spatial variability masked temporal changes in the mineral soil of Lithic Leptosols (Skeltic), whereas a significant reduction of Pb concentrations in their forest floors occurred. Reductions of concentrations in the less heterogeneous Cambisols (Chromic) were significant. In contrast, virtually no migration of Pb and Cd were found in Stagnosols due to their impeded drainage. Very low element concentrations (<1 μg l−1) in field-collected soil solutions using tension lysimeters (0.2 μm nylon filters) imply that migration largely occurred by preferential flow as particulate-bound species during intensive rainfall events. Our results indicate that the extent of Pb and Cd migration in soils is largely influenced by soil type. 相似文献
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长江流域常量元素的分布特征 总被引:1,自引:0,他引:1
2003年4月到5月对长江干流及主要支流河水中常量元素(Ca 2+,K+,Na+,Mg2+,Cl-,SO2-4及碱度)进行了测定,并对常量元素的含量及影响因素进行了研究。结果表明,长江阳离子以钙为主,占阳离子总量的40%~80%;而阴离子主要为HCO-3,占阴离子总量的60%~90%;阴阳离子含量顺序为HCO-3>SO2-4>Cl-,Ca 2+>Na+ >Mg 2+>K+。长江干流及主要支流河水的常量离子主要来自于岩石的风化,主要受碳酸盐类溶解的控制,硅酸盐类的风化过程较弱。而大气沉降的影响很小,只有SO2-4受大气沉降影响较大。长江干流的Na+、Mg2+、Ca2+、HCO-3和Cl-主要来自于上游,下游只是对上游的简单稀释,而没有额外来源。与世界上其它大河相比,长江的常量离子浓度处于较高的水平;温带地区的河流河水中常量离子的含量常处于较高的水平;热带地区的河流河水中常量离子的含量相对较低。 相似文献
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K. M. S. Sundaram A. Sundaram 《Journal of environmental science and health. Part. B》2013,48(5):453-473
Abstract Spray deposit patterns were measured on aluminum coils and live balsam fir needles at different canopy heights, following aerial application of mexacarbate (4‐dimethylamino‐3,5‐xylyl N‐methylcarbamate) over a conifer forest in New Brunswick. Droplet size spectra of the spray cloud were determined on cylindrical Kromekote® cards placed at the corresponding crown heights. Ground deposits were collected on cylindrical Kromekote cards, aluminum coils and natural balsam fir foliage placed In forest clearings and under different types of vegetation. Canopy deposits decreased progressively from the top to the bottom level of the tree crown. This trend was observed on aluminum coils, live fir foliage, and Kromekote cards. Droplet size spectra were similar at all sampling heights of the tree crown, and were comparable to those obtained on the ground cards placed in the forest clearings. Deposits of mexacarbate obtained on ground samplers on the open forest floor were markedly lower than those found at the top canopy but were similar to those at the mid or bottom canopy level. Droplet size spectra and mexacarbate deposits obtained on samplers placed under different types of forest vegetation indicated a selective filtration of the large droplets present in the spray cloud by plant canopies. 相似文献
68.
A human health risk assessment of rare earth elements in soil and vegetables from a mining area in Fujian Province,Southeast China 总被引:1,自引:0,他引:1
Contaminated food through dietary intake has become the main potential risk impacts on human health. This study investigated concentrations of rare earth elements (REEs) in soil, vegetables, human hair and blood, and assessed human health risk through vegetables consumption in the vicinity of a large-scale mining area located in Hetian Town of Changting County, Fujian Province, Southeast China. The results of the study included the following mean concentrations for total and bio-available REEs of 242.92 ± 68.98 (135.85–327.56) μg g−1 and 118.59 ± 38.49 (57.89–158.96) μg g−1 dry weight (dw) in agricultural soil, respectively, and total REEs of 3.58 ± 5.28 (0.07–64.42) μg g−1 dw in vegetable samples. Concentrations of total REEs in blood and hair collected from the local residents ranged from 424.76 to 1274.80 μg L−1 with an average of 689.74 ± 254.25 μg L−1 and from 0.06 to 1.59 μg g−1 with an average of 0.48 ± 0.59 μg g−1 of the study, respectively. In addition, a significant correlation was observed between REEs in blood and corresponding soil samples (R2 = 0.6556, p < 0.05), however there was no correlation between REEs in hair and corresponding soils (p > 0.05). Mean concentrations of REEs of 2.85 (0.59–10.24) μg L−1 in well water from the local households was 53-fold than that in the drinking water of Fuzhou city (0.054 μg L−1). The health risk assessment indicated that vegetable consumption would not result in exceeding the safe values of estimate daily intake (EDI) REEs (100−110 μg kg−1 d−1) for adults and children, but attention should be paid to monitoring human beings health in such rare earth mining areas due to long-term exposure to high dose REEs from food consumptions. 相似文献
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《Chemosphere》2013,93(10):2473-2479
One hundred and twelve soil samples were collected from residential areas surrounding a coal-fired power plant at Huainan City, Anhui Province, China. The concentrations of environmentally sensitive elements (ESEs As, Cd, Cr, Cu, Hg, Mn, Ni, Pb, V and Zn) in soil samples were determined, and their potential ecological and health risks were assessed. Mean concentrations of ESEs in the downwind soils of the power plant are relatively higher than those in the upwind soils, pointing to a potential ESEs input from coal combustion. The calculated ecological risk of ESEs in soils indicates a relatively low ecological risk. Hazard quotient (HQ) of ESEs in downwind soils is 1.5, suggesting a potential health risk for children. However, the carcinogenic risk values of ESEs in soils are within the acceptable non-hazardous range of 1E−06–1E−04. 相似文献
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Due to the wide occurrence of endocrine disrupting chemicals in the environment, it is much of importance to develop high throughput screening method for the analysis of this kind of pollutants. Using anion-exchange membrane chromatography, vitellogenin (VTG) from the plasma of 17β-estradiol (E2) treated Chinese rare minnow was rapidly purified within 15 min. Both polyclonal antibody (PcAb) and monoclonal antibody (McAb) against rare minnow VTG (R-VTG) were prepared in rabbit and Balb/c mice, respectively. The competitive enzyme-linked immunosorbent assays (ELISA) based on either PcAb or McAb were developed to identify and quantify R-VTG in the plasma, and these two methods showed similar characteristics. The detection limits of both assays were lower than 3 ng mL−1 with the working ranges covering three magnitudes. The recovery efficiencies of PcAb and McAb based ELISA were 104.2% and 102.6%, respectively; and the intra-assay and inter-assay of these two assays were 6.2% and 9.2%, 8.6% and 12.8%, respectively. These results indicated that the described competitive ELISA methods were sensitive and valuable tools for quantifying vitellogenin in rare minnow plasma. These methods were then applied to measure R-VTG concentrations in plasma of male fish exposed to a series of E2 concentrations. When E2 levels were less than 10 ng L−1, R-VTG levels in plasma were comparable to that in solvent control, while R-VTG levels significantly increased 15-folds and 350-folds, respectively when E2 exposure concentrations were controlled at 10 and 50 ng L−1. The high sensitivity of Chinese rare minnow to E2 was demonstrated, making it a valuable model species to study environmental estrogens. 相似文献