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11.
对中国城市环境地质工作的思考   总被引:9,自引:1,他引:9  
本文回顾了国内外城市地质工作的发展历程,阐述了中国城市地质工人的发展方向和重点工作领域。指出城市地质工作必须服务于城市(城市群,经济开发区)的规划,建设和管理,为城市社会经济可持续发展,减灾防灾提供具有针对性,实用性和超前性的基础地质资料和成果。由于中国城市的规模,性质,自然资源承载力,地质环境特征不同,城市环境地质调查,评价的对象,内容也将有所差异。归纳起来,城市地质的重点工作领域为:城市可持续发展,城市可持续发展的资源开发战略与对策,城市地质环境容量及脆弱性分析。城市地质灾害:城市地质灾害风险,影响面,易损性及对灾害的反应,城市环境变化的地质指标体系,城市环境地质综合研究:城市环境地质调查评价的新理论,新方法,新技术,城市环境地质图纱的编制。数字城市环境地质:GIS平台上的地质空间数据库,城市地质环境动态分析,评价,决策系统和地质灾害预警预报系统。  相似文献   
12.
This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H2O2, UV/TiO2 and UV/K2S2O8 (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H2O2 process, and the higest removal rate even reached to 83%. UV/TiO2 and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H2O2 was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.  相似文献   
13.
Hyporheic exchange is known to provide an important control on nutrient and contaminant fluxes across the stream-subsurface interface. Similar processes also mediate interfacial transport in other permeable sediments. Recent research has focused on understanding the mechanics of these exchange processes and improving estimation of exchange rates in natural systems. While the structure of sediment beds obviously influences pore water flow rates and patterns, little is known about the interplay of typical sedimentary structures, hyporheic exchange, and other transport processes in fluvial/alluvial sediments. Here we discuss several processes that contribute to local-scale sediment heterogeneity and present results that illustrate the interaction of overlying flow conditions, the development of sediment structure, pore water transport, and stream-subsurface exchange. Layered structures are shown to develop at several scales within sediment beds. Surface sampling is used to analyze the development of an armor layer in a sand-and-gravel bed, while innovative synchrotron-based X-ray microtomography is used to observe patterns of grain sorting within sand bedforms. We show that layered bed structures involving coarsening of the bed surface increase interfacial solute flux but produce an effective anisotropy that favors horizontal pore water transport while limiting vertical penetration.  相似文献   
14.
Stream restoration projects are often based on morphological form or stream type and, as a result, there needs to be a clear tie established between form and function of the stream. An examination of the literature identifies numerous relationships in naturally forming streams that link morphologic form and stream processes. Urban stream restoration designs often work around infrastructure and incorporate bank stabilization and grade control structures. Because of these imposed constraints and highly altered hydrologic and sediment discharge regimens, the design of urban channel projects is rather unclear. In this paper, we examine the state of the art in relationships between form and processes, the strengths and weaknesses of these existing relationships, and the current lack of understanding in applying these relationships in the urban environment. In particular, we identify relationships that are critical to urban stream restoration projects and provide recommendations for future research into how this information can be used to improve urban stream restoration design. It is also suggested that improving the success of urban restoration projects requires further investigation into incorporating process-based methodologies, which can potentially reduce ambiguity in the design and the necessity of using an abundant amount of in-stream structures.  相似文献   
15.
通过大气细颗粒物实时在线源解析技术(质谱直接测量法)采集录入淮安市市区部分特征污染源排放成分谱,对淮安市大气细颗粒物进行在线源解析,获取高时间分辨的颗粒物源解析结果,分析颗粒物来源、季度变化和重污染天气的污染过程,评估形成重污染过程的污染影响因子和影响程度,为区域大气污染综合整治提供重要目标指向,同时也为淮安环境空气PM2.5重度污染实时预警与监控、大气污染源减排方案评估、污染事件监控等提供有效的在线监测技术平台.  相似文献   
16.
海洋中丙烯酸的研究进展   总被引:1,自引:0,他引:1  
丙烯酸是海洋中的短链脂肪酸,是海洋中主要含硫化合物DMSP(dimethylsulfoniopropionate,β-二甲基巯基丙酸内盐)裂解的产物之一。本文综述了海洋中丙烯酸的来源、性质、在海洋中的作用以及海水中丙烯酸的测定方法。通过观测海水中丙烯酸的含量、分布及生物地球化学循环过程,有助于了解丙烯酸对海洋生态系统碳循环和硫循环的贡献。并对海洋中丙烯酸的进一步研究提出了展望。  相似文献   
17.
Achievement of at least “good ecological status” in all waterbodies under the EU Water Framework Directive by 2015 will in some cases be a challenge. The twin challenge is to manage expectations of policy makers for such waterbodies as to a realistic length of time required for improvement in water quality. Hence, understanding the source, transformation processes and residence time of nitrate in a hydrological system is an essential part of meeting such challenges. On a dairy farm with 24 shallow groundwater wells, the dual isotopic composition of nitrate (δ15N and δ18O) was used to clarify nitrate sources, to assess spatial and temporal variability in nitrate concentrations and to determine if and where denitrification was occurring. Vertical travel time was estimated to correlate nitrate concentrations with management practices. Organically derived nitrogen was the predominant source contributing to groundwater nitrate concentrations. Denitrification was identified as prevalent within specific regions of the study site. The distinct low temporal variability in the isotopic data suggests constancy among nitrate sources and processes over time across the study site. Vertical travel times of up to 3 years were estimated on site indicating the influence of recent management practices on nitrate concentrations. Very slow horizontal migration of groundwater (decades) indicates a legacy of older management practices. Stable isotope techniques, together with an understanding of time lag, provide an extra mechanism to test the efficacy of monitoring and mitigation programmes.  相似文献   
18.
施工张拉控制是张弦网壳结构的关键技术之一,提出采用控制索原长的反分析方法追踪结构施工整个过程。首先,通过控制索在预应力状态下的张拉力求出零状态和索原长,并同时获得预应力态下所有单元的内力。在此基础上,通过控制每一级张拉索的原长,进行非线性有限元迭代计算,可求出索在分级分批施工时的控制力,并用VC++6.0编制相应的计算程序。这一方法有效地避免了通用有限元需要反复试算,计算繁琐的缺点。最后,以张弦网壳结构模型为试验对象,按分级分批张拉的方式模拟结构的现场施工,并跟踪施工过程中杆件单元的应力状态。结果表明,数值模拟计算与试验值吻合较好,计算结果可靠,该方法能精确模拟结构的施工成形过程,且在整个过程中,每根索只需张拉一次,简化了施工工艺。  相似文献   
19.
黄河口不同恢复阶段湿地土壤N2O产生的不同过程及贡献   总被引:3,自引:1,他引:2  
采用时空替代法,选择黄河口生态恢复前后未恢复区(R0)、2007年恢复区(R2007)和2002年恢复区(R2002)的芦苇湿地为研究对象,分析了生态恢复工程对湿地土壤N2O产生不同过程与贡献的影响.结果表明,尽管不同恢复阶段湿地土壤N2O总产生量差异明显,但总体均表现为N2O释放.恢复区湿地土壤的N2O产生量大于未恢复区.N2O的产生主要以硝化作用和硝化细菌反硝化作用为主,而反硝化作用对N2O的产生有较大削弱作用,这与不同恢复阶段湿地土壤理化性质密切相关.非生物作用对N2O产生量贡献较大,这与黄河口为高活性铁区,Fe的还原作用关系密切.尽管黄河口不同恢复阶段湿地土壤N2O的产生是生物作用与非生物作用共同作用的结果,但由于非生物作用对N2O产生的影响较大,应受到特别关注.温度和水分对不同恢复阶段湿地土壤N2O产生过程的影响不尽一致,这与土壤微生物活性对温度和水分的响应差异有关.黄河口不同恢复阶段湿地土壤的N2O总产生量介于(0.37±0.08)~(9.75±7.64)nmol·(kg·h)-1,略高于闽江口互花米草湿地的N2O总产生量,但明显低于富氧森林土壤、草原土壤和闽江口短叶茳芏湿地的N2O总产生量.研究发现,黄河口生态恢复工程的长期实施明显促进了N2O的产生,因而下一步生态恢复工程应统筹考虑景观恢复与温室气体削弱这两方面因素.  相似文献   
20.
BACKGROUND: Synthetic musk compounds are widely used as additives in personal care and household products. The photochemical degradation of musk tibetene in aqueous solutions or in acetonitrile/water mixtures under different conditions was studied in order to assess its environmental fate. METHODS: Musk tibetene dissolved (or suspended) in water and/or acetonitrile/water mixtures was irradiated at different times by UV-light and by solar light. The irradiation mixtures were analyzed by NMR and TLC. The photoproducts formed were identified by GC-MS and NMR data. RESULTS: The experimental results indicated that musk tibetene was photodegradable in water or acetonitrile/water mixtures with half-life reaction times close to 20 minutes. The irradiation mixtures were separated by chromatographic techniques yielding three photoproducts (3,3,5,6,7-pentamethyl-4-nitro-3H-indole, 3,3,5,6,7-pentamethyl-4-nitro-1H-indoline and 3,3,5,6,7-pentamethyl-4-nitro-3H-indolinone) identified by means of spectroscopic analysis. DISCUSSION: The numerical modelling of the photodegradation concentration-time profiles gave (8.13 +/- 0.15) x 10(-2) and (1.34 +/- 0.04) x 10(-2) mol/E for the overall primary quantum yield of direct photolysis for musk tibetene and the major intermediate (3,3,5,6,7-pentamethyl-4-nitro-3H-indolinone), respectively, in the wavelength range 305-366 nm. The half-life times of photodegradation of the both substances varied from 1-1.5 hours at 20 degrees N during the summer season to 6-10 hours for highest latitudes in winter. CONCLUSIONS: Under solar light, musk tibetene was photolabile in acetonitrile and acetonitrile/water 1/1, while it was slowly degraded when suspended in water. In all media, musk tibetene was photodegraded into three photoproducts. By using a kinetic model, the overall primary quantum yields of direct photolysis of musk tibetene and its main photoproduct, in the wavelength range 305-366 nm, were estimated, indicating that the photodegradation rate for musk tibetene is faster than the photolysis rate of the major by-product. RECOMMENDATIONS AND PERSPECTIVES: The results indicate that, in order to assess the environmental impact of musk tibetene on the aquatic ecosystem, great attention should be focused on the major photoproduct which is proved to be more persistent than the parent compound under light irradiation. The predicted half-life times of direct photolysis for both substances ranged from 1-1.5 hours at 20 degrees N during the summer season to about 6-10 hours for highest latitudes in winter, indicating that, from a photochemical point of view, the environmental persistence of these substances increases by increasing the latitudes and during the cold seasons, making more realistic an intake of these xenobiotic molecules into the food chain of aquatic living organisms. Tanabe reports in his Editorial (Tanabe 2005) that "It is necessary to have knowledge of the global picture of synthetic musk pathways. So, it is conceivable that now is the time to study the transport, persistency, distribution, bioaccumulation and toxic potential of this new environmental menace on a global scale, especially in developing countries". Therefore, the future environmental analysis and investigations on the eco-toxicity of nitro musk compounds should take into account not only the presence of the parent compounds but also their photochemical intermediates or end-by-products.  相似文献   
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