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61.
环境雌激素生物效应的作用机制研究进展   总被引:2,自引:0,他引:2  
环境雌激素(environmental estrogens,EEs)种类繁多,来源多样且分布广泛,大量工业添加剂、食品添加剂和农药类物质已被证实具有雌激素活性。EEs对人体生殖、神经、免疫等系统的生物毒性已经引起了公众的普遍关注。近年来的研究表明,EEs不仅结合雌激素核受体(nuclear estrogen receptor,n ER),还可以活化雌激素膜受体(membrane estrogen receptor,m ER),干扰正常的雌激素信号通路。本文总结了EEs通过n ER、m ER介导的多种雌激素基因组和非基因组信号途径及其产生的生物学效应,综述了在其毒理学作用机理基础上发展的环境样品的雌激素活性评估和EEs混合物的联合作用研究,以期为该类污染物的筛查、风险评估和进一步的机制研究提供参考。  相似文献   
62.
三唑酮在水环境中的环境行为、毒性效应及生态风险   总被引:1,自引:0,他引:1  
三唑酮是目前应用最广泛的三唑类广谱杀菌剂之一,在我国的使用量有逐年增长的趋势。本研究综述了三唑酮在水环境中的环境行为、毒性效应及其对我国部分水体的生态风险。三唑酮使用后被土壤吸附和解吸,经雨水淋溶作用进入地表或地下水环境,在丰水期检出率与检出浓度较高,目前我国地表水中三唑酮最高检出浓度为12μg·L-1。三唑酮在环境中的半衰期为15~43.3 d,能够在水生生物体内累积代谢,在不同浓度下对不同类群、不同生命阶段的水生生物表现出不同的毒性效应,对应着多条有害结局路径,其中最重要的是通过抑制细胞色素P450酶活性干扰机体内激素水平,影响水生生物繁殖和生长发育,导致种群密度降低。在目前已知的暴露水平下,三唑酮对我国地表水具有潜在的生态风险,特别是丰水期稻田附近的地表水风险尤其需要关注。  相似文献   
63.
为研究稳定浓度目标下温室气体排放路径的不确定性问题,应用温室气体导致气候变化评估模型( MAGICC模型)和WRE排放情景的数据对2100年温室气体浓度控制在450和550 ppmvCO2当量目标下的排放路径及浓度变化情况进行了研究.结果显示,目标年浓度的变化取决于起始年至目标年的累计排放量和摊放路径.将排放路径峰值逐渐调整滞后时,为保证累计排放量不变,需在到达峰值后比原排放路径进行更大力度的减排.温室气体浓度在预测期内将逐渐增加,但目标年的结果变化较小,约为浓度变化最大值的1/3左右.将WRE350和WRE450排放路径的峰值分别调整至2020年和2035年时,与原排放路径相比,浓度改变的最大值分别为6.4 ppmv和22.8 ppmv,而2100年浓度的改变值分别为1.9 ppmv和7.5 ppmv.  相似文献   
64.
Extreme climate events, floods, and drought, cause huge impact on daily lives. In order to produce society resilient to extreme events, it is necessary to assess the impact of frequent and high intensity storm events on design parameters. This article describes a methodology to develop future peak “design discharges” throughout the United States that can be used as a guidance to map future floodplains. In order to develop a lower and upper limit for anticipated peak flow discharges, two future growth scenarios — Representative Concentration Pathways (RCPs)‐RCP 2.6 and 8.5 were identified as the weak and strong climate scenario respectively based on the output from the global climate models. The Generalized Least Square technique in United States Geological Survey's Weighted Multiple Regression (WREG) program was used to develop regression equations that relate peak discharges to basin and climate parameters of the contributing watershed. The design discharges reflect the most recent climate model results. Number of frost days, heavy rainfall days, high temperature days, and snow depth were found to be the common extreme climate parameters influencing the regression equations. This methodology can be extended to other flood frequency events if rainfall data is available. The future discharges can be utilized in hydraulics models to estimate floodplains that can assist in resilient infrastructure planning and outline climate change adaptation strategies.  相似文献   
65.
社会技术转型的多层视角(MLP)是转型理论的最新进展,它认为转型是由三个层面——微观层的技术利基,中观层的社会技术体制和宏观层的大环境——相互作用引起的一个非线性的演化过程。该思路通过分析技术和社会因素之间的互动关系,寻求理解社会技术体制的长期变化。本文以MLP为分析思路,研究我国电力系统现行体制已经发生的动态变化;并从短期,中期和长期三个时间维度,对我国低碳电力系统转型路径提出一个概念性的分析框架。短期的转变路径,延续和发展现有体制结构和治理模式,通过体制内行为主体有意识地调整创新活动和发展的方向,来解决体制内部矛盾和压力,实现政府2020年的减排目标和可再生能源目标。中期的重构路径,基本实现电源结构实质性改变,火力发电比例逐步下降,可再生能源发电对其主导地位形成冲击和挑战,电力系统呈现百花齐放百家争鸣之势态。长期的重置路径通过新的低碳能源技术创新的质的突破和飞跃,实现高煤高碳的电力体系由新的低碳体制取代这一长期目标。本文从理论和方法上丰富了目前我国低碳转型的讨论,对政策制定者和相关的行为主体也可提供一种有益的参考。  相似文献   
66.
Food consumption has been widely reported to be the main source of human exposure to PCBs. A total of 47 samples of food products on sale in supermarkets in the United Kingdom were thus analyzed for PCBs to determine residual levels in oil and oil-based products. The objective was to compare the measured levels of total PCBs (ΣPCBs) in food products to those reported in various environmental compartments. Combined extraction and online clean up was achieved using Accelerated Solvent Extraction? (ASE) to recover target analytes for analysis by GC-MSD (gas chromatography mass spectrometry). Σ PCBs (ng/g) in each product were in the ranges of 4.73–44.38 edible oil; 1.40–6.18 mayonnaise; 1.21–6.25 salad cream; 1.28–5.64 seafood sauce, and 0.97–15.08 exotic dressing. The level of human exposure to PCBs in all products was < 1 μg/kg body weight/day when considering a 70 kg male or 57 kg female, possibly reflecting the reported decline of PCBs in the environment.  相似文献   
67.
As an active metabolite of venlafaxine and emerging antidepressant, O-desmethylvenlafaxine (ODVEN) was widely detected in different water bodies, which caused potential harm to human health and environmental safety. In this study, the comparative work on the ODVEN degradation by UV (254 nm) and UV-LED (275 nm) activated sodium percarbonate (SPC) systems was systematically performed. The higher removal rate of ODVEN can be achieved under UV-LED direct photolysis (14.99%) than UV direct photolysis (4.57%) due to the higher values of photolysis coefficient at the wavelength 275 nm. Significant synergistic effects were observed in the UV/SPC (80.38%) and UV-LED/SPC (53.57%) systems and the former exhibited better performance for the elimination of ODVEN. The degradation of ODVEN all followed the pseudo-first-order kinetics well in these processes, and the pseudo-first-order rate constant (kobs) increased with increasing SPC concentration. Radicals quenching experiments demonstrated that both ·OH and CO3· were involved in the degradation of ODVEN and the second-order rate constant of ODVEN with CO3· (1.58 × 108 (mol/L)−1 sec−1) was reported for the first time based on competitive kinetic method. The introduction of HA, Cl, NO3 and HCO3 inhibited the ODVEN degradation to varying degrees in the both processes. According to quantum chemical calculation, radical addition at the ortho-position of the phenolic hydroxyl group was confirmed to be the main reaction pathways for the oxidation of ODVEN by ·OH. In addition, the oxidation of ODVEN may involve the demethylation, H-abstraction, OH-addition and C-N bond cleavage. Eventually, the UV-LED/SPC process was considered to be more cost-effective compared to the UV/SPC process, although the UV/SPC process possessed a higher removal rate of ODVEN.  相似文献   
68.
一种新型环境污染物:羟基化多溴联苯醚(OH-PBDEs)   总被引:1,自引:0,他引:1  
张长  胡浪平  曾光明  蒋敏  马晓莹  余健 《环境科学》2011,32(7):2169-2176
近年来羟基化多溴联苯醚(OH—PBDEs)在诸多环境介质中陆续被检出,其中一些被证明能在生物体内蓄积,另外一些被证明能产生致毒效应.作为一种新型的有机污染物,OH—PBDEs逐渐成为环境工作者研究的新热点.本文介绍了OH-PBDEs在环境中的来源及暴露水平,概述了国内外最近几年关于OH-PBDEs的环境浓度检测、生物体...  相似文献   
69.
Climate change mitigation, in the context of growing population and ever increasing economic activity, will require a transformation of energy and agricultural systems, posing significant challenges to global water resources. We use an integrated modelling framework of the water-energy-land-climate systems to assess how changes in electricity and land use, induced by climate change mitigation, impact on water demand under alternative socioeconomic (Shared Socioeconomic Pathways) and water policy assumptions (irrigation of bioenergy crops, cooling technologies for electricity generation). The impacts of climate change mitigation on cumulated global water demand across the century are highly uncertain, and depending on socioeconomic and water policy conditions, they range from a reduction of 15,000 km3 to an increase of more than 160,000 km3. The impact of irrigation of bioenergy crops is the most prominent factor, leading to significantly higher water requirements under climate change mitigation if bioenergy crops are irrigated. Differences in socioeconomic drivers and fossil fuel availability result in significant differences in electricity and bioenergy demands, in the associated electricity and primary energy mixes, and consequently in water demand. Economic affluence and abundance of fossil fuels aggravate pressures on water resources due to higher energy demand and greater deployment of water intensive technologies such as bioenergy and nuclear power. The evolution of future cooling systems is also identified as an important determinant of electricity water demand. Climate policy can result in a reduction of water demand if combined with policies on irrigation of bioenergy, and the deployment of non-water-intensive electricity sources and cooling types.  相似文献   
70.

Several peripheral metabolic pathways can be used by microorganisms to degrade toxic aromatic compounds that are known to pollute the environment. Hydroxyquinol (1,2,4-trihydroxybenzene) is one of the central intermediates in the degradative pathway of a large variety of aromatic compounds. The present review describes the microorganisms involved in the degradative pathway, the key enzymes involved in the formation and splitting of the aromatic ring of (chloro)hydroxyquinol as well as the central intermediates formed. An attempt was also made to provide some estimation for genetic basis of the hydroxyquinol pathway.  相似文献   
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