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排序方式: 共有908条查询结果,搜索用时 343 毫秒
721.
Mooshammer M Wanek W Schnecker J Wild B Leitner S Hofhansl F Blöchl A Hämmerle I Frank AH Fuchslueger L Keiblinger KM Zechmeister-Boltenstern S Richter A 《Ecology》2012,93(4):770-782
Resource stoichiometry (C:N:P) is an important determinant of litter decomposition. However, the effect of elemental stoichiometry on the gross rates of microbial N and P cycling processes during litter decomposition is unknown. In a mesocosm experiment, beech (Fagus sylvatica L.) litter with natural differences in elemental stoichiometry (C:N:P) was incubated under constant environmental conditions. After three and six months, we measured various aspects of nitrogen and phosphorus cycling. We found that gross protein depolymerization, N mineralization (ammonification), and nitrification rates were negatively related to litter C:N. Rates of P mineralization were negatively correlated with litter C:P. The negative correlations with litter C:N were stronger for inorganic N cycling processes than for gross protein depolymerization, indicating that the effect of resource stoichiometry on intracellular processes was stronger than on processes catalyzed by extracellular enzymes. Consistent with this, extracellular protein depolymerization was mainly limited by substrate availability and less so by the amount of protease. Strong positive correlations between the interconnected N and P pools and the respective production and consumption processes pointed to feed-forward control of microbial litter N and P cycling. A negative relationship between litter C:N and phosphatase activity (and between litter C:P and protease activity) demonstrated that microbes tended to allocate carbon and nutrients in ample supply into the production of extracellular enzymes to mine for the nutrient that is more limiting. Overall, the study demonstrated a strong effect of litter stoichiometry (C:N:P) on gross processes of microbial N and P cycling in decomposing litter; mineralization of N and P were tightly coupled to assist in maintaining cellular homeostasis of litter microbial communities. 相似文献
722.
723.
Chelate assisted phytoextraction of heavy metals from soil. Effect, mechanism, toxicity, and fate of chelating agents 总被引:12,自引:0,他引:12
The low-cost, plant-based phytoextraction technique has often been described as a promising technique to remediate heavy metal contaminated agricultural land. The application of chelating agents has shown positive effects in increasing the solubility of heavy metals in soil and therefore in enhancing phytoextraction. This paper gives an overview of the chelating agents applied in recent studies. Various synthetic aminopolycarboxylic acids, such as ethylene diamine tetraacetic acid, and natural ones such as, ethylene diamine disuccinate and nitrilotriacetic acid, are described. Additionally, results of the application of natural low molecular weight organic acids, such as citric and tartaric acid are given. The effectiveness of these different chelating agents varies according to the plant and the heavy metals used. Furthermore, a focus is laid on the chelating agents fate after application and on its toxicity to plants and soil microorganisms, as well as it degradation. The rate of degradation is of great importance for the future of chelate assisted phytoextraction as it has a direct impact on the leaching probability. An effective prevention of leaching will be crucial for the acceptance and the economic breakthrough of enhanced phytoextraction, but a satisfactory solution to this key issue has so far not been found. Possibly further experiments in the field of enhanced phytoextraction will be able to solve this major problem, but over decades various greenhouse experiments and recently field experiments have resulted in different observations. Therefore, it is questionable if further research in this direction will lead to a promising solution. Phytoextraction has possibly reached a turning point in which it should distance itself from chelate assisted phytoextraction and focus on alternative options. 相似文献
724.
Organic aerosols in the Miami area, USA: temporal variability of atmospheric particles and wet/dry deposition 总被引:1,自引:0,他引:1
Atmospheric particulate matter and both wet and dry deposition was collected over a period of nine months at one location in the metropolitan area of Miami, Florida. Molecular distributions and concentrations of n-alkanes, fatty acids, polycyclic aromatic hydrocarbons (PAHs) and hopanes were determined using weekly composite samples over this time period in order to determine temporal variability, and their possible dependence on climatic parameters such as temperature, rainfall and wind direction and frequency. Based on molecular distributions of the compounds studied, potential emission sources for the atmospheric particles were assessed and suggested to be mainly derived from automobile exhaust and natural sources. Although wet and dry deposition processes were observed to remove about equal amounts of organic aerosols from the Miami atmosphere, dry deposition was dominant in the removal of anthropogenically derived compounds such as PAHs and hopanes. Only very limited seasonal trends were observed, while wind direction and frequency was found to be the most important meteorological parameter controlling the temporal variability of the organic aerosols. This is the first detailed report of this nature for the Miami area. 相似文献
725.
726.
苏丹红Ⅰ、Ⅲ和Ⅳ对HepG-2细胞和SGC-7901细胞增殖的影响 总被引:4,自引:0,他引:4
以辽宁某地硼矿开采和加工厂的硼作业工人以及远离硼矿的背景地区的人群作为研究对象,分析了班后尿液硼浓度与日硼暴露剂量之间的关系.结果表明,班后尿硼浓度与日硼暴露剂量之间存在着显著的对数线性关系,考虑了不同人群类别的影响之后,回归方程的拟合度达到85.9%,由此确立了用班后尿硼浓度预测日硼暴露剂量的预测方程.用此预测方程对本研究2004年的受试者日硼暴露剂量进行预测,并与实测值进行了比较,结果表明平均相对偏差为13.4%,预测值与实测值之间没有显著性的差异.说明用班后尿硼浓度预测日硼暴露剂量是可行的.对2004年所有受试者的日硼暴露剂量预测结果分析表明,硼职业暴露组、社区对照组和背景对照组的日硼暴露剂量平均值分别为36.1、4.13和1.31mg/d. 相似文献
727.
728.
729.
730.
Ten years of atmospheric methane observations at a high elevation site in Western China 总被引:3,自引:0,他引:3
L.X. Zhou D.E.J. Worthy P.M. Lang M.K. Ernst X.C. Zhang Y.P. Wen J.L. Li 《Atmospheric environment (Oxford, England : 1994)》2004,38(40):7041-7054
In this paper, the continuous (1994–2001) and discrete air sample (1991–2001) measurements of atmospheric CH4 from the Waliguan Baseline Observatory located in western China (36°17′N, 100°54′E, 3816 m asl) are presented and characterized. The CH4 time series show large episodic events on the order of 100 ppb throughout the year. During spring, a diurnal cycle with average amplitude of 7 ppb and a morning maximum and late afternoon minimum is observed. In winter, a diurnal cycle with average amplitude of 14 ppb is observed with an afternoon maximum and morning minimum. Unlike most terrestrial observational sites, no obvious diurnal patterns are present during the summer or autumn. A background data selection procedure was developed based on local horizontal and vertical winds. A selected hourly data set representative of “baseline” conditions was derived with approximately 50% of the valid hourly data. The range of CH4 mixing ratios, annual means, annual increases and mean annual cycle at Waliguan during the 1992–2001 were derived from discrete and continuous data representative of “baseline” conditions and compared to air samples collected at other Northern Hemisphere sites. The range of CH4 monthly means of 1746–1822 ppb, average annual means of 1786.7±10.8 ppb and mean annual increase of 4.5±4.2 ppb yr−1 at Waliguan were inline with measurements from sites located between 30° and 60°N. There were variations observed in the CH4 annual increase patterns at Waliguan that were slightly different from the global pattern. The mean CH4 annual cycle at Waliguan shows an unusual pattern of two gentle peaks in summer and February along with two small valleys in early winter and spring and a mean peak-to-peak amplitude of 11 ppb, much smaller than amplitudes observed at most other mid- and high-northern latitude sites. The Waliguan CH4 data are strongly influenced by continental Asian CH4 emissions and provide key information for global atmospheric CH4 models. 相似文献