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121.
袁志英  郝江南 《地球与环境》2005,33(Z1):251-254
本文系笔者对贵阳地区主要地质环境和工程地质特点进行的初步总结,内容为贵阳地区主要岩土构成情况、分布范围及与之相应的岩土工程地质特点和主要的岩土工程地质问题的描述,旨在给同行提供宏观性的了解和方向性的参考。  相似文献   
122.
大气CO2浓度升高对农田生态系统的影响   总被引:1,自引:0,他引:1  
自由大气CO2浓度升高(简称FACE,即Free A ir CO2Enrichment)对陆地生态系统的影响是全球变化研究中的一个热点。综述了FACE条件下,农田土壤植物生物量质量变化和土壤微生物对植物的反馈作用,以及土壤痕量气体排放的趋势变化。  相似文献   
123.
安徽月山地区的成岩-成矿作用在长江中下游地区具一定的典型性。本文论述了月山地区成岩-成矿的时空关系,探讨了岩浆岩及岩浆演化的成矿作用显示,并从成矿地球化学角度深入研究了闪长质岩浆(岩)对两类铜矿床成矿物质来源的贡献,从而确定了月山地区成岩-成矿作用的内在联系,评价了岩浆岩体的成矿潜力。  相似文献   
124.
Quantity of trace arsenic in grain and soil was determined by hydride nondispersive atomic fluorescence method.Optimum conditions of measurement were selected in the experiment including the pH of the medium, reductive agent, the concentration and flowing velocity of KBH4, rate of carrier gas and atomized temperature. The reference sample of rice C was determined and the linear relationship of the calibration curve was plotted, indicating that the method was highly precise. In the experiment of recovery rate, the method was quite satisfactory.Based on the determination of hundreds of samples, it is proved that atomic fluorescence method is rapid, sensitive and low in interference. It is very efficient on determination of trace arsenic in soils and grains, especially in grains.  相似文献   
125.
红壤中结合态磷在酸化条件下的变化及其相互关系   总被引:12,自引:1,他引:12  
以浙江沿海地区的红壤为研究对象,通过浸滤过程,研究了在酸化条件下,红壤中可溶笥结合态磷的变化和它们之间的相关关系,结果显示,红壤中可溶性Fe-P比Ca-P、Al-P对酸度的变化更为敏感;当红壤中可溶性磷的原始含量较高时,随酸度的增强从固相中释出的趋势更明显;在酸化过程中、红壤中不同可溶性结合态磷之间呈现出不同的相关关系,这归因子它们对酸化敏感性的差异。  相似文献   
126.
福建省森林固定CO2价值评估   总被引:10,自引:0,他引:10  
借鉴国内外研究成果,引入“市场逼近系数”,构造森林固定CO2效益经济结构模型,评估福建省森林固定CO2价值,为福建省森林资源的科学管理和资产评估提供了借鉴和参考。  相似文献   
127.
Potential for carbon sequestration in Canadian forests and agroecosystems   总被引:2,自引:0,他引:2  
The potential for carbon (C) sequestration was examined in selectedCanadian forest settings and prairie agroecosystems under severalmanagement scenarios. A simple C budget model was developed toquantitatively examine C sequestration potential in living biomass of forestecosystems, in associated forest-product C pools, and in displaced fossil-fuelC. A review of previous studies was conducted to examine C sequestrationpotential in prairie agroecosystems. In the forest settings examined, ourwork suggests that substantial C sequestration opportunities can be realizedin the short term through the establishment of protected forest-C reserves.Where stands can be effectively protected from natural disturbance, peaklevels of biomass C storage can exceed that under alternative managementstrategies for 200 years or more. In settings where it is not feasible tomaintain protected forest-C reserves, C sequestration opportunities can berealized through maximum sustained yield management with harvestedbiomass put towards the displacement of fossil fuels. Because there is afinite capacity for C storage in protected forest-C reserves, harvesting forestbiomass and using it to displace the use of fossil fuels, either directlythrough the production of biofuels or indirectly through the production oflong-lived forest products that displace the use of energy-intensive materialssuch as steel or concrete, can provide the greatest opportunity to mitigategreenhouse gas emissions in the long term. In Canadian prairieagroecosystems, modest C sequestration can be realized while enhancingsoil fertility and improving the efficiency of crop production. This can bedone in situations where soil organic C can be enhanced without relianceupon ongoing inputs of nitrogen fertilizer, or where the use of fossil fuelsin agriculture can be reduced. More substantial C offsets can be generatedthrough the production of dedicated energy crops to displace the use offossil fuels. Where afforestation or reconstruction of native prairieecosystems on previously cultivated land is possible, this represents thegreatest opportunity to sequester C on a per unit-area basis. However,these last two strategies involve the removal of land from crop production,and so they are not applicable on as wide a scale as some other Csequestration options which only involve modifications to currentagricultural practices.  相似文献   
128.
IntroductionContaminationofediblevegetationbypersistent,ubiquitouschemicalssuchasPCBs,dioxins,pesticides,andherbicidesprovidesamajorexposureroutetohumans ,domesticanimalsandwildlife .Uptakeoftheseorganicchemicalsbyplant,andsubsequentdistributionintheplan…  相似文献   
129.
Based on wet air oxidation (WAO) and Fenton reagent, thispaper raises a new low pressure wet catalytic oxidation(LPWCO)which requires low pressure for the treatment of highlyconcentrated and refractory organic wastewater. Compared withgeneral wet air oxidation, the pressure of the treatment(0.1-0.6MPa) is only one of tens to percentage of latter(3.5-10MPa). Inaddition, its temperature is no more than 180℃.Compared withFenton reagent, while H2O2/COD(weight ratio) less than 1.2, theremoval of COD in the treatment is over twenty percents more thanFenton's even the value of COD is more than 14000mg/L. In thispaper, we study the effect factor of COD removal and the mechanismof this treatment. The existence of synergistic effect (catalytic oxidation and carbonization) for COD removal in H2SO4-Fenton reagent system under the condition of applied pressure and heating (0.1-0.6MPa, 104-165℃) was verified. The best condition of this disposal are as follows:H2O2/COD(weight ratio)=0.2-1.0, Fe2+ 0.6×10-3 mol, H2SO4 0.5mol, COD>1×104mg/L, the operating pressure is 0.1-0.6MPa and temperature is 104-165℃. This method suit to dispose the high-concentrated refractory wastewater, especially to the wastewater containing H2SO produced in the manufacture of pesticide, dyestuff and petrochemical works.  相似文献   
130.
A total of 198 agricultural soil samples were collected from Zhangjiagang and Changshu in Southern Jiangsu for analysis of 13 polychlorinated biphenyls (PCBs) in order to assess the levels of pollution, sources, area distribution, and potential risk for the environment. All methods were rigorously tested and an adequate quality control was ensured. Only one site had no PCBs residues, and the highest total PCBs concentration in the surface soils was 32.83 ng/g. The average concentration in all the soil samples was 4.13 ng/g, signaling low-level pollution. Tetra-, penta-, and hexa-chlorinated biphenyls were dominant species in soil samples, accounting for more than 75% ofΣPCBs in the soil samples. PCB118 was the most abundant congener in all the samples. The PCB118 was about 20% ofΣPCBs. The soil organic matter content showed only a weak correlation with the levels of all PCB congeners, in which a better correlation was noted for the more volatile lighter PCB congeners than for the heavier homologues. To a certain extent, the sources and land use seemed to influence the levels of PCBs.  相似文献   
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