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471.
地下土壤、水中DNAPLs污染的修复技术研究进展   总被引:2,自引:1,他引:1  
综述了国内外地下土壤、含水层DNAPLs污染的迁移机理及其修复技术研究进展,对该领域的研究前景做了展望.  相似文献   
472.
建立了一种基质固相分散萃取—气相色谱法测定土壤中8种有机氯农药含量的方法,优选了固相分散剂及其用量、洗脱溶剂以及土壤样品与分散剂的质量比.实验结果表明,在弗罗里硅土作为分散剂、正己烷和丙酮(体积比为1:1)为洗脱溶剂、土壤样品与分散剂的质量比为1:3的优化条件下,8种有机氯农药在50~250μg/kg范围内表现出良好的...  相似文献   
473.
生物质炭对Cd污染土壤团聚体酶活性的影响   总被引:2,自引:0,他引:2  
为探究生物质炭对Cd污染土壤团聚体酶活性的影响,采用盆栽试验,向模拟Cd污染土壤中添加生物质炭并测定水稻根际土壤团聚体碳循环酶与氧化还原酶活性.结果表明:Cd污染土壤团聚体酶活性对添加量为2.5%的生物质炭响应明显,氧化还原酶活性指数值介于0.522~0.792之间.在2.5mg/kg的外源Cd条件下,2.5%的生物质...  相似文献   
474.
针对生物炭作为新型土壤改良剂的研究进展,介绍了生物炭制备方法,分析了生物炭与土壤重金属作用机制,探讨了生物炭联用技术.分析认为:原料、热解温度、热解时间等制备条件对生物炭去除重金属效果有不同程度的影响,热解温度影响程度最高,可以通过优化热解温度等条件制备生物炭;生物炭与土壤重金属间有直接和间接两种作用方式,不同生物炭与...  相似文献   
475.
介绍了STW型生态土壤稳定剂对宁淮高速公路边坡膨胀土的胀缩性、水稳性、强度、抗冲刷性等的改性试验研究,并结合现场试验,分析了STW型生态土壤稳定剂用于膨胀土边坡坡面防护的效果。试验结果表明:STW型生态土壤稳定剂改性膨胀土的胀缩性,随着稳定剂掺量的增大而减小;改性土的水稳性,随着稳定剂稀释浓度的增大而增强;同时,改性土的强度得到显著提高,抗冲刷性能得到明显增强,具有显著的防治水土流失、促进表层固化、提高坡面稳定的效果。  相似文献   
476.
白腐真菌修复多环芳烃污染土壤及其降解机理的研究进展   总被引:3,自引:0,他引:3  
介绍了白腐真菌对多环芳烃(PAHs)的代谢途径、降解机理,阐述了白腐真菌修复PAHs污染土壤的影响因素和生态效应,并提出了提高白腐真菌修复效率的措施.白腐真菌主要通过分泌木质素降解酶系(木质家过氧化物酶、锰过氧化物酶和漆酶)来降解PAHs,这些胞外酶可通过开环作用把PAHs代谢成为水溶性较强的醌类中间产物,再由其他微生物降解这些中间产物直至矿化.在白腐真菌的培养过程中.通过对环境因素及营养条件(如温度、pH值、C/N比、微量元素和转速)的优化可提高胞外酶产量.在修复PAHs污染土壤过程中,生物竞争、营养条件和环境因素等均会影响白腐真菌的修复效果.同时,归纳总结了改善白腐真菌修复效果的一些措施,如真菌-细菌联合修复、添加适当的培养基质、添加表面活性剂、直接施用酶制剂和改善营养条件等.  相似文献   
477.
研究了地下土壤渗滤系统在农村生活污水处理中的应用,并详细地比较了面积分别为9,45,90m^2以及200m^2的处理系统在工程实际中出水水质的不同。实验结果表明,随着土地处理系统面积的增大,出水的各个水质指标(CODcr、BOD5、TP、NH3-N)相应变好。结合施工、运行及管理等方面的优点,推荐收集各户生活污水再集中建设土地处理系统,系统面积在90—300m^2之间。  相似文献   
478.
To understand the effects of long-term amendment of organic manure and N fertilizer on N2O emission in the North China Plain, a laboratory incubation at different temperatures and soil moistures were carried out using soils treated with organic manure (OM), half organic manure plus half fertilizer N (HOM), fertilizer NPK (NPK), fertilizer NP (NP), fertilizer NK (NK), fertilizer PK (NK) and control (CK) since 1989. Cumulative N2O emission in OM soil during the 17 d incubation period was slightly higher than in NPK soil under optimum nitrification conditions (25℃ and 60% water-filled pore space, WFPS), but more than twice under the optimum denitrification conditions (35℃ and 90% WFPS). N2O produced by denitrification was 2.1-2.3 times greater than that by nitrification in OM and HOM soils, but only 1.5 times greater in NPK and NP soils. These results implied that the long-term amendment of organic manure could significantly increase the N2O emission via denitrification in OM soil as compared to NPK soil. This is quite different from field measurement between OM soil and NPK soil. Substantial inhibition of the formation of anaerobic environment for denitrification in field might result in no marked difference in N2O emission between OM and NPK soils. This is due in part to more rapid oxygen diffusion in coarse textured soils than consumption by aerobic microbes until WFPS was 75% and to low easily decomposed organic C of organic manure. This finding suggested that addition of organic manure in the tested sandy loam might be a good management option since it seldom caused a burst of N2O emission but sequestered atmospheric C and maintained efficiently applied N in soil.  相似文献   
479.
Carbon mineralization and its response to climatic warming have been receiving global attention for the last decade. Although the virtual influence of temperature effect is still in great debate, little is known on the mineralization of organic carbon (SOC) of paddy soils of China under warming. SOC mineralization of three major types of China's paddy soils is studied through laboratory incubation for 114 d under soil moisture regime of 70% water holding capacity at 20℃ and 25℃ respectively. The carbon that mineralized as CO2 evolved was measured every day in the first 32 d and every two days in the following days. Carbon mineralized during the 114 d incubation ranged from 3.51 to 9.22 mg CO2-C/gC at 20℃ and from 4.24 to 11.35 mg CO2-C/gC at 25℃ respectively; and a mineralizable C pool in the range of 0.24 to 0.59 gC/kg, varying with different soils. The whole course of C mineralization in the 114 d incubation could be divided into three stages of varying rates, representing the three subpools of the total mineralizable C: very actively mineralized C at 1-23 d, actively tnineralized C at 24--74 d and a slowly mineralized pool with low and more or less stabilized C mineralization rate at 75-114 d. The calculated Q10 values ranged from 1.0 to 2.4, varying with the soil types and N status. Neither the total SOC pool nor the labile C pool could account for the total mineralization potential of the soils studied, despite a well correlation of labile C with the shortly and actively mineralized C, which were shown in sensitive response to soil warming. However, the portion of microbial C pool and the soil C/N ratio controlled the C mineralization and the temperature dependence. Therefore, C sequestration may not result in an increase of C mineralization proportionally. The relative control of C bioavailability and microbial metabolic activity on C mineralization with respect to stabilization of sequestered C in the paddy soils of China is to be further studied.  相似文献   
480.
Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.  相似文献   
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