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91.
周年磷肥旱季集中底施对玉-稻轮作磷肥效应的影响   总被引:1,自引:0,他引:1  
春玉米-晚稻水旱轮作是近年来南方稻区种植制度变化下出现的新型两熟制模式。明确两季作物间磷肥的合理分配对玉-稻轮作作物产量与磷素利用效率的影响,对玉-稻轮作养分高效与高产协同实现,及丰富对水旱轮作前后季作物养分利用关系的认识具有理论意义。采用春玉米-水稻周年轮作田间试验,根据晚稻季磷肥前移至玉米季做底肥施用的比例及周年施磷量,设置7个磷肥施用处理,分别为两季作物均不施磷(P_0)、两季作物均按常规方法施磷(P_1)、1/3晚稻季磷肥前移(P_2)、2/3晚稻季磷肥前移(P_3)、全部晚稻季磷肥前移(P_4)、全部晚稻季磷肥前移且周年总施磷量减少15%(P_5)、全部晚稻季磷肥前移且周年总施磷量减少30%(P_6),分析了不同施磷处理作物产量、磷素吸收量及磷素利用效率的变化。与P_1相比,P_3与P_4处理显著提高了晚稻花后干物质的分配比例及晚稻产量,且其周年产量分别提高了4.87%和6.74%;P_5处理晚稻产量与P_1处理差异不显著,但P_6显著降低了晚稻产量。晚稻季磷肥前移施用明显促进了玉米及晚稻对磷素的吸收,显著降低了磷素的表观盈余量。与P_1处理相比,P_2、P_3、P_4处理两季作物周年土壤磷素依存率分别减少了11.63%、26.47%与22.08%。从磷肥利用效率看,P_4处理的磷肥周年累积回收效率、农学利用效率、偏生产力及磷肥产量贡献率均显著高于P_1处理,分别提高了102.46%、194.83%、6.73%与176.16%。与P_1处理相比,P_5处理周年磷肥产量贡献率及农学利用效率差异不显著,但分别提高了其磷肥回收效率与偏生产力32.56%和58.05%。玉米季施用的磷肥对晚稻有明显的后效作用,且比晚稻季施用磷肥具有更高的磷肥利用效率。所以在春玉米免耕复种晚稻时,可将晚稻季的磷肥全部前移至玉米季施用,并可减少15%周年施磷量。  相似文献   
92.
Conservation and development practitioners increasingly promote community forestry as a way to conserve ecosystem services, consolidate resource rights, and reduce poverty. However, outcomes of community forestry have been mixed; many initiatives failed to achieve intended objectives. There is a rich literature on institutional arrangements of community forestry, but there has been little effort to examine the role of socioeconomic, market, and biophysical factors in shaping both land‐cover change dynamics and individual and collective livelihood outcomes. We systematically reviewed the peer‐reviewed literature on community forestry to examine and quantify existing knowledge gaps in the community‐forestry literature relative to these factors. In examining 697 cases of community forest management (CFM), extracted from 267 peer‐reviewed publications, we found 3 key trends that limit understanding of community forestry. First, we found substantial data gaps linking population dynamics, market forces, and biophysical characteristics to both environmental and livelihood outcomes. Second, most studies focused on environmental outcomes, and the majority of studies that assessed socioeconomic outcomes relied on qualitative data, making comparisons across cases difficult. Finally, there was a heavy bias toward studies on South Asian forests, indicating that the literature on community forestry may not be representative of decentralization policies and CFM globally.  相似文献   
93.
Plastic waste is a source of organic contaminants such as hexabromocyclododecanes (HBCDs). HBCDs have been found to cause developmental and reproductive toxicity; it is important to investigate the occurrence and metabolization of HBCDs in the soil environments with plastic waste contamination. This work analyzed HBCDs and their metabolites in soil and plant samples collected from Xinle and Dingzhou—the major plastic waste recycling centers in North China. Results showed that total HBCD concentrations in soils followed the order: plastic waste treatment site (11.0–624 ng/g) > roadside (2.96–85.4 ng/g) ≥ farmland (8.69–55.5 ng/g). HBCDs were detected in all the plant samples with total concentrations ranging from 3.47 to 23.4 ng/g. γ-HBCD was the dominant congener in soils, while α-HBCD was preferentially accumulated in plants. Compositions of HBCD isomers in soils and plants were significantly different (P < 0.05) among sampling sites and among plant species. HBCDs in farmland soil and all plant samples exhibited high enantio-selectivity based on the enantiomeric fractions (EFs). Furthermore, metabolites of pentabromocyclododecenes (PBCDEs) were frequently identified in soils, and mono-OH-HBCDs were the most common ones in plants. This study for the first time provides evidences of HBCD contamination in the soil-plant system caused by plastic waste, their stereo-selectivity, and metabolization behavior, improving our understanding of the environmental behavior and fate of HBCDs.  相似文献   
94.
Hsu JF  Guo HR  Wang HW  Liao CK  Liao PC 《Chemosphere》2011,83(10):1353-1359
Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) are unintentional byproducts of combustion and industrial processes. Firefighters face the risk of occupational exposure to PCDD/Fs. Congener-specific analyses of 17 PCDD/Fs were performed on 20 serum samples collected from firefighters and fire scene investigators, and four soot samples that had deposited on the surfaces of the fire helmets and were collected after the firefighters had fought fires. The PCDD/F concentrations on the helmets that were contaminated by being worn at the fire scenes were 63-285 times higher than those on a clean helmet. The median serum PCDD/F concentration of the 16 firefighters (12 pg WHO2005-TEQ g−1 lipid) was not different from those of the males from the general Taiwanese population (9.4 pg WHO2005-TEQ g−1 lipid). However, the median PCDD/F level in the four fire scene investigators (15 pg WHO2005-TEQ g−1 lipid) was higher than those in the male from the general Taiwanese population (Mann-Whitney U test, p < 0.01). Furthermore, the serum samples from the firefighters and fire scene investigators, and the soot samples from the fire scenes presented similarly distinctive PCDD/F profiles that had elevated proportions for 10 PCDF congeners. Limited data indicated that the fire scene investigators were occupationally exposed to PCDD/Fs at the fire scenes. We suggested that the firefighters were not occupationally exposed to PCDD/Fs at the fire scenes due to appropriate protection. However, the fire scene investigators may have had more occupational exposure to PCDD/Fs due to poor protection, and further research must be performed to confirm this.  相似文献   
95.
Modifications of black carbons and their influence on pyrene sorption   总被引:2,自引:0,他引:2  
Zhang W  Wang L  Sun H 《Chemosphere》2011,85(8):1306-1311
Sorption of pyrene on black carbons (BCs) obtained by heating sawdust at two temperatures (400 and 700 °C, denoted as 400BC and 700BC, respectively), as well as on modified BCs (via oxidation, oximation, and hydrolysis) was studied to investigate the role of BC structural characteristics in sorption of hydrophobic organic compounds. Pyrene was bound strongly by 700BC and 400BC, with organic carbon normalized distribution coefficients (Koc) of 105.04-105.86 and 104.65-105.16, respectively, at equilibrium pyrene concentrations of 10-100 μg L−1. Both chemical composition and pore distribution of the two BCs changed after modifications, which led to changes in their sorption characteristics for pyrene. After modifications, the linearity of pyrene sorption isotherm increased for 700BC but decreased for 400BC. For 700BC, both oxidation and oximation reduced pyrene sorption, with Koc decreasing by 69.1-73.7% and 18.7-33.9%, respectively, whereas hydrolysis did not exert a significant influence. For 400BC, oxidation and hydrolysis reduced Koc by 2.28-25.9% and 29.2-33.9%, respectively, while oximation increased Koc. In most cases, the change in sorption capacity could be explained by the changes in C content and type, polarity, surface area, and micropore volume of the BCs; however, the role of conformation (the accessibility to sorption sites) could not be ignored.  相似文献   
96.
Environmental Science and Pollution Research - The scientific knowledge produced by academic research can be valued in all sectors of human activity, including private sector. The ROVALTAIN...  相似文献   
97.
Environmental Science and Pollution Research - It is of great significance for the coordinated development of the environment and the economy to study the impact of the human driving factors of...  相似文献   
98.
Environmental Science and Pollution Research - The livestock manure nitrogen load on farmland (LMNLF) is often used to assess the potential environmental pollution risk of livestock manure nitrogen...  相似文献   
99.
Environmental Science and Pollution Research - Paspalum distichum L. was tested to evaluate their phytoremediation capacity for Hg contaminated soil through analyzing the dissipation of Hg in soil...  相似文献   
100.
Environmental Science and Pollution Research - Soil erosion threatens environmental sustainability worldwide. Exploring the trajectories of soil erosion and associated drivers is of great...  相似文献   
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