全文获取类型
收费全文 | 833篇 |
免费 | 28篇 |
国内免费 | 81篇 |
专业分类
安全科学 | 45篇 |
废物处理 | 6篇 |
环保管理 | 116篇 |
综合类 | 330篇 |
基础理论 | 55篇 |
污染及防治 | 160篇 |
评价与监测 | 137篇 |
社会与环境 | 58篇 |
灾害及防治 | 35篇 |
出版年
2024年 | 1篇 |
2023年 | 24篇 |
2022年 | 13篇 |
2021年 | 16篇 |
2020年 | 22篇 |
2019年 | 16篇 |
2018年 | 22篇 |
2017年 | 11篇 |
2016年 | 15篇 |
2015年 | 15篇 |
2014年 | 36篇 |
2013年 | 35篇 |
2012年 | 28篇 |
2011年 | 66篇 |
2010年 | 35篇 |
2009年 | 60篇 |
2008年 | 57篇 |
2007年 | 51篇 |
2006年 | 35篇 |
2005年 | 21篇 |
2004年 | 24篇 |
2003年 | 19篇 |
2002年 | 27篇 |
2001年 | 24篇 |
2000年 | 29篇 |
1999年 | 27篇 |
1998年 | 35篇 |
1997年 | 32篇 |
1996年 | 11篇 |
1995年 | 27篇 |
1994年 | 22篇 |
1993年 | 13篇 |
1992年 | 25篇 |
1991年 | 8篇 |
1990年 | 6篇 |
1989年 | 5篇 |
1988年 | 2篇 |
1987年 | 4篇 |
1986年 | 5篇 |
1985年 | 11篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 2篇 |
1978年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有942条查询结果,搜索用时 395 毫秒
261.
262.
从风险物质数量、风险诱发因素及风险防控能力角度出发,采用加权评分法,结合周边环境敏感受体情况,对沈阳市某化工园现状做环境风险评估。结果表明:JHYSD和XJHX的区域环境风险值贡献最大,分别为3.08和2.59,约占园区内总风险值的41.2%;该化工园综合环境风险值为13.57,构成该综合风险值的各分项大小不同,其中,RIS_(危险废物)分项环境风险最大,贡献率达到28.89%,其次为RIS_(大气),贡献率达27.34%,其余三者顺序为RIS_(化学品)RIS_水RIS_(累积)。 相似文献
263.
随着各地雾霾等大气污染问题反复出现,各种复杂的大气环境质量问题开始在全球集中呈现。大气污染物在环流扰动之下已经开始了长距离传输,不再是过去单纯的点源污染,而是表现出了蔓延速度更加迅速、污染更加复杂的情况,加强大气环境监测工作刻不容缓。因此本文以大气环境质量现状为出发点,对目前我国大气环境质量监测中存在的问题进行了分析,并就此提出了完善我国大气环境质量监测工作的对策,希望能推动我国大气环境质量的进一步改善。 相似文献
264.
上海市浦东新区作为承接国家自由贸易区的先行试点地区,近年来吸引大批国内外企业入驻,同时经济发展与环境友好型社会矛盾依然突出。本文以2014年-2018年来浦东新区区域噪音与交通噪数据为依据,分析本地区声环境状况,结果表明声环境质量有所下降,一类功能区及交通噪音需进一步加强治理。通过源头屏蔽,大力发展张江、周浦、滴水湖等科技园区建设,阻断企业对居民区的噪声影响等措施,进而提升和改善浦东新区声环境质量状况。 相似文献
265.
以四川农业大学成都校区为监测点,采用大气主动采样法(AA)、大气干表面法(ADS)及大气湿表面法(AWS)3种常用干沉降采集方法做大气磷干沉降通量对比试验。结果表明,3种采样方法获得的大气磷干沉降通量间具有显著的差异性及相关性(P0.05),三者间可以进行换算统一;AA法适用于较短采样周期的连续性监测研究,ADS法适用于较长采样周期(5 d)的监测研究,而AWS法更适用于在长采样周期(月)内选取一段时间作为干沉降监测的研究。 相似文献
266.
C. Leroy 《Journal of environmental radioactivity》2010,101(11):937-944
Atmospheric releases of krypton-85, from the nuclear fuel reprocessing plant at the AREVA NC facility at La Hague (France), were used to test Gaussian models of dispersion. In 2001-2002, the French Institute for Radiological Protection and Nuclear Safety (IRSN) studied the atmospheric dispersion of 15 releases, using krypton-85 as a tracer for plumes emitted from two 100-m-high stacks. Krypton-85 is a chemically inert radionuclide. Krypton-85 air concentration measurements were performed on the ground in the downwind direction, at distances between 0.36 and 3.3 km from the release, by neutral or slightly unstable atmospheric conditions. The standard deviation for the horizontal dispersion of the plume and the Atmospheric Transfer Coefficient (ATC) were determined from these measurements. The experimental results were compared with calculations using first generation (Doury, Briggs) and second generation (ADMS 4.0) Gaussian models. The ADMS 4.0 model was used in two configurations; one takes account of the effect of the built-up area, and the other the effect of the roughness of the surface on the plume dispersion. Only the Briggs model correctly reproduced the measured values for the width of the plume, whereas the ADMS 4.0 model overestimated it and the Doury model underestimated it. The agreement of the models with measured values of the ATC varied according to distance from the release point. For distances less than 2 km from the release point, the ADMS 4.0 model achieved the best agreement between model and measurement; beyond this distance, the best agreement was achieved by the Briggs and Doury models. 相似文献
267.
Soil inventories of anthropogenic radionuclides were investigated in altitudinal transects in 2 French regions, Savoie and Montagne Noire. Rain was negligible in these 2 areas the days after the Chernobyl accident. Thus anthropogenic radionuclides are coming hypothetically only from Global Fallout following Atmospheric Nuclear Weapon Tests. This is confirmed by the isotopic signatures (238Pu/239+240Pu; 137Cs/239+240Pu; and 241Am/239+240Pu) close to Global Fallout value. In Savoie, a peat core age-dated by 210Pbex confirmed that the main part of deposition of anthropogenic radionuclides occurred during the late sixties and the early seventies. In agreement with previous studies, the anthropogenic radionuclide inventories are well correlated with the annual precipitations. However, this is the first time that a study investigates such a large panel of annual precipitation and therefore of anthropogenic radionuclide deposition. It seems that at high-altitude sites, deposition of artificial radionuclides was higher possibly due to orographic precipitations. 相似文献
268.
E. Bagnato M. Sproveri M. Barra M. Bitetto M. Bonsignore S. Calabrese V. Di Stefano E. Oliveri F. Parello S. Mazzola 《Chemosphere》2013
The first attempt to systematically investigate the atmospheric mercury (Hg) in the MBL of the Augusta basin (SE Sicily, Italy) has been undertaken. In the past the basin was the receptor for Hg from an intense industrial activity which contaminated the bottom sediments of the Bay, making this area a potential source of pollution for the surrounding Mediterranean. Three oceanographic cruises have been thus performed in the basin during the winter and summer 2011/2012, where we estimated averaged Hgatm concentrations of about 1.5 ± 0.4 (range 0.9–3.1) and 2.1 ± 0.98 (range 1.1–3.1) ng m−3 for the two seasons, respectively. These data are somewhat higher than the background Hgatm value measured over the land (range 1.1 ± 0.3 ng m−3) at downtown Augusta, while are similar to those detected in other polluted regions elsewhere. Hg evasion fluxes estimated at the sea/air interface over the Bay range from 3.6 ± 0.3 (unpolluted site) to 72 ± 0.1 (polluted site of the basin) ng m−2 h−1. By extending these measurements to the entire area of the Augusta basin (∼23.5 km2), we calculated a total sea–air Hg evasion flux of about 9.7 ± 0.1 g d−1 (∼0.004 t yr−1), accounting for ∼0.0002% of the global Hg oceanic evasion (2000 t yr−1). The new proposed data set offers a unique and original study on the potential outflow of Hg from the sea–air interface at the basin, and it represents an important step for a better comprehension of the processes occurring in the marine biogeochemical cycle of this element. 相似文献
269.
270.
2006年秋冬两季图们市大气气溶胶中多环芳烃分布规律 总被引:1,自引:0,他引:1
大气气溶胶是目前大多数城市的首要污染物,其中的多环芳烃是对人体健康危害最大的环境污染物之一。通过图们市2006年9月、12月4个采样点的大气气溶胶样品分析,研究了大气气溶胶中多环芳烃的分布规律。采用超声波萃取法提取样品中的多环芳烃,然后对其进行旋蒸浓缩,氮气吹至1ml,用高效液相色谱进行定性和定量分析。实验结果表明,美国EPA优先控制的16种多环芳烃普遍存在于图们市区的大气气溶胶中。图们市不同时空大气气溶胶中多环芳烃的分布具有一定的规律性。 相似文献