全文获取类型
收费全文 | 648篇 |
免费 | 10篇 |
国内免费 | 79篇 |
专业分类
安全科学 | 1篇 |
废物处理 | 3篇 |
环保管理 | 80篇 |
综合类 | 206篇 |
基础理论 | 99篇 |
污染及防治 | 199篇 |
评价与监测 | 121篇 |
社会与环境 | 26篇 |
灾害及防治 | 2篇 |
出版年
2024年 | 1篇 |
2023年 | 5篇 |
2022年 | 16篇 |
2021年 | 7篇 |
2020年 | 12篇 |
2019年 | 12篇 |
2018年 | 10篇 |
2017年 | 17篇 |
2016年 | 29篇 |
2015年 | 20篇 |
2014年 | 25篇 |
2013年 | 70篇 |
2012年 | 37篇 |
2011年 | 85篇 |
2010年 | 37篇 |
2009年 | 57篇 |
2008年 | 55篇 |
2007年 | 38篇 |
2006年 | 31篇 |
2005年 | 15篇 |
2004年 | 22篇 |
2003年 | 21篇 |
2002年 | 18篇 |
2001年 | 17篇 |
2000年 | 13篇 |
1999年 | 5篇 |
1998年 | 16篇 |
1997年 | 11篇 |
1996年 | 2篇 |
1995年 | 5篇 |
1994年 | 6篇 |
1993年 | 3篇 |
1992年 | 4篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1980年 | 1篇 |
1978年 | 1篇 |
1973年 | 1篇 |
1968年 | 1篇 |
排序方式: 共有737条查询结果,搜索用时 31 毫秒
271.
Heavy metal contamination in surface sediments of Yangtze River intertidal zone: An assessment from different indexes 总被引:4,自引:0,他引:4
Weiguo Zhang Jinna Chang Hongxia Xie 《Environmental pollution (Barking, Essex : 1987)》2009,157(5):1533-1543
Surface sediments (0-5 cm) from 59 stations within the Yangtze River intertidal zone (YRIZ) were sampled for metal contamination analysis in April and August 2005. The concentrations ranged (in mg kg−1 dry weight): Al, 40,803-97,213; Fe, 20,538-49,627; Cd, 0.12-0.75; Cr, 36.9-173; Cu, 6.87-49.7; Mn, 413-1,112; Ni, 17.6-48.0; Pb, 18.3-44.1; and Zn, 47.6-154; respectively. Among the 59 sampling stations, enrichment factors (EF) indicate enrichment of Cd (52 stations), Cr (54 stations), Cu (5 stations), Ni (26 stations), Pb (5 stations) and Zn (5 stations). Geoaccumulation indexes (Igeo) also suggest individual metal contamination in localized areas. This study indicates that Cd, Cr and Ni enrichment in the YRIZ sediment is widespread whereas Cu, Mn, Pb and Zn enrichment is localized or nonexistent. Factor and cluster analyses indicate that Cd is associated with total organic carbon whereas Cu, Cr, Ni, Pb and Zn have a close association with Mn. 相似文献
272.
Kristina L. Sundqvist Mats Tysklind Ingemar Cato Anders Bignert Karin Wiberg 《Environmental science and pollution research international》2009,16(4):396-409
Background, aim, and scope The primary aim of this study was to explore the variations in PCDD/F levels and homologue profiles of Baltic surface sediments
by comprehensively analyzing polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) in samples from a large number of sites, encompassing not only previously
known hotspot areas, but also sites near other potential PCDD/F sources, in pristine reference areas (in which there was no
industrial activity) and offshore sites.
Materials and methods Surface sediment samples (146 in total) were collected at various points along the Swedish coast and offshore areas. In addition,
bulk deposition was sampled, monthly, at a single site in northern Sweden during 1 year. The concentrations of tetra- through octa-substituted CDD/Fs were determined in both matrices.
Results Highly elevated concentrations of PCDD/Fs were found at many sites in coastal areas and concentrations were also slightly
elevated in some offshore areas. Homologue profiles varied substantially amongst samples from coastal sites, while those from
offshore and other pristine sediments were relatively similar. The offshore sediments showed different profiles from those
observed in the deposition samples. Sediment levels of PCDD/Fs were not generally significantly correlated to organic carbon
levels, except in some pristine areas. Comparison of data obtained in this and previous studies suggest that both their levels
and profiles are similar today to those observed 20 years ago in coastal and offshore areas. The only detected trend is that
their levels appear to have decreased slightly in the offshore area of the Bothnian Sea.
Discussion The localization of hotspot areas along the coast, the lack of consensus between PCDD/F profiles of sediments and general
background, and their weak correlations with organic carbon suggest that PCDD/Fs in the study area largely originate from
local/regional emissions. However, due to complicating factors such as sediment dynamics and land upheaval, it is not possible
to conclude whether these pollutants derive from recent emissions or from a combination of recent emissions and re-distribution
of previous inputs.
Conclusions The results show that: elevated levels of PCDD/Fs are present in both coastal and offshore areas of the Baltic Sea, the major
hotspots are close to the shore, and there are large variations in profiles, indicating that local emissions are (or have
been) the major causes of pollution.
Recommendations and perspectives In order to identify other hotspot areas and trace sources, comprehensive analysis of PCDD/Fs in surface sediments is needed
in all areas of the Baltic Sea that have not been previously investigated. The high levels of PCDD/Fs observed in surface
sediments also indicate a need to elucidate whether they are due mainly to current emissions or a combination of recent pollution
and re-distribution of historically deposited pollutants. To do so, better understanding of sediment dynamics and present-day
inputs, such as riverine inputs, industrial effluents, and leakage from contaminated soil is required. There are indications
that contaminated sediments have a regional impact on fish contamination levels. However, as yet there is no statistically
robust evidence linking contaminated sediments with elevated levels in Baltic biota. It should also be noted that the Baltic
Sea is being massively invaded by the deep-burrowing polychaete Marenzielleria ssp., whose presence in sediments has been shown to increase water concentrations of hydrophobic pollutants. In awareness
of this, it is clear that high levels in sediments cannot be ignored in risk assessments. In order to investigate the emission
trends more thoroughly, analysis of PCDD/Fs in offshore sediment cores throughout the Baltic Sea is also recommended.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
273.
Landscape Planning for Agricultural Nonpoint Source Pollution Reduction III: Assessing Phosphorus and Sediment Reduction Potential 总被引:2,自引:0,他引:2
Riparian buffers have the potential to improve stream water quality in agricultural landscapes. This potential may vary in
response to landscape characteristics such as soils, topography, land use, and human activities, including legacies of historical
land management. We built a predictive model to estimate the sediment and phosphorus load reduction that should be achievable
following the implementation of riparian buffers; then we estimated load reduction potential for a set of 1598 watersheds
(average 54 km2) in Wisconsin. Our results indicate that land cover is generally the most important driver of constituent loads in Wisconsin
streams, but its influence varies among pollutants and according to the scale at which it is measured. Physiographic (drainage
density) variation also influenced sediment and phosphorus loads. The effect of historical land use on present-day channel
erosion and variation in soil texture are the most important sources of phosphorus and sediment that riparian buffers cannot
attenuate. However, in most watersheds, a large proportion (approximately 70%) of these pollutants can be eliminated from
streams with buffers. Cumulative frequency distributions of load reduction potential indicate that targeting pollution reduction
in the highest 10% of Wisconsin watersheds would reduce total phosphorus and sediment loads in the entire state by approximately
20%. These results support our approach of geographically targeting nonpoint source pollution reduction at multiple scales,
including the watershed scale. 相似文献
274.
吹扫捕集-GC-MS测定废水中的硝基氯苯 总被引:1,自引:0,他引:1
建立了吹扫捕集-GC-MS测定水样中硝基氯苯类化合物的方法.考察了吹扫温度、吹扫时间等对吹扫捕集效率和方法检出限的影响.在室温下,当吹扫时间为30 min时,该方法的最低检出限可达0.002 mg/L,工作曲线的线性范围为2×10 -3 ~2 mg/L,相对标准偏差在2%~6%,加标回收率在97.0%~110.0%.与国家标准方法相比,该法具有操作简便、灵敏度高、线性范围宽且无须使用有毒有机溶剂等优点,可满足工业废水和地表水中硝基氯苯的测定要求. 相似文献
275.
Heavy metal content and distribution in surface sediments of the Seyhan River, Turkey 总被引:4,自引:0,他引:4
Davutluoglu OI Seckin G Ersu CB Yilmaz T Sari B 《Journal of environmental management》2011,92(9):2250-2259
Chemical fractionation of seven heavy metals (Cd, Cr, Cu, Mn, Ni, Pb and Zn) was studied using a modified three-step sequential procedure to assess their impacts in the sediments of the Seyhan River, Turkey. Samples were collected from six representative stations in two campaigns in October 2009 and June 2010, which correspond to the wet and dry seasons, respectively. The total metal concentrations in the sediments demonstrated different distribution patterns at the various stations. Cadmium was the only metal that was below detection at all stations during both sampling periods. Metal fractionation showed that, except for Mn and Pb, the majority of metals were found in the residual fraction regardless of sampling time, indicating that these metals were strongly bound to the sediments. The potential mobility of the metals (non-residual fractions) is reflected in the following ranking: Pb > Mn > Zn > Cu > Ni > Cr in October 2009 and Mn > Pb > Zn > Cu > Ni > Cr in June 2010. The second highest proportion of metals was bound to organic matter/sulfides, originating primarily from anthropogenic activities. Non-residual metal fractions for all stations were highest in June 2010, which may be linked to higher organic matter concentrations in the sediment samples with 1.40% and 15.1% in October 2009 and June 2010, respectively. Potential sediment toxicity was evaluated using the Risk Assessment Code (RAC). Based on RAC classification, Cd and Cr pose no risk, Cu and Ni pose low risk, Pb and Zn were classified as medium risk metals, while the environmental risk from Mn was high. In addition, based on the sediment quality guidelines (SQG), the Seyhan River can be classified as a river with no, to moderate, toxicological risks, based on total metal concentrations. 相似文献
276.
277.
Arsenic fractionation and contamination assessment in sediments of thirteen lakes from the East Plain and Yungui Plateau Ecoregions, China 总被引:2,自引:0,他引:2
Fengyu Zan Shouliang Huo Jingtian Zhang Li Zhang Beidou Xi Lieyu Zhang 《环境科学学报(英文版)》2014,26(10):1977-1984
Arsenic(As) fractions in the sediments of seven lakes from East Plain Ecoregion and six lakes from Yungui Plateau Ecoregion, China, were investigated. Results indicated that the total As concentrations in sediment samples of lakes of the East Plain Lake Ecoregion are higher than those of Yungui Plateau Lake Ecoregion. Residual As is the main fraction in sediment samples of lakes from both ecoregions, followed by reducible As and soluble or oxidizable As. The total As is correlated to oxidizable As and residual As in sediment samples from both lake ecoregions. As distribution in sediment samples of lakes of the East Plain Ecoregion appears to be affected by human activity, while the As origin mainly comes from natural sources in sediment samples of lakes in the Yungui Plateau Ecoregion. The potential ecological risk index and geoaccumulation index values suggest "low to moderate" risk degree and "unpolluted to moderately polluted" for As in the studied lake sediments. 相似文献
278.
279.
松花江表层沉积物有毒重金属污染的潜在生物毒性风险评价 总被引:5,自引:2,他引:5
采用地累积指数模型(Igeo)及一致性沉积物质量基准(CBSQGs)对第二松花江、松花江干流以及4条代表性支流12个断面表层沉积物Hg、Cd、Cr、As和Pb 5种有毒重金属的污染特征及其潜在生物毒性风险进行深入探讨.研究结果表明:1松花江表层沉积物中5种重金属含量平均值由大到小顺序为CrPbAsCdHg;除Hg外,其余4种重金属均表现为一定的富集现象,但富集系数不超过1.2;2地累积指数表明松花江表层沉积物中5种有毒重金属污染较轻,基本属于无污染或无污染-轻污染状态,只有Cr和As在10号断面达到了轻污染程度;3重金属之间Pearson相关系数表明Cr和As(0.896)、Cr和Pb(0.708)呈极显著相关,As和Pb呈显著相关(0.639),揭示Cr、As和Pb极可能具有相似的来源;4各断面毒性单位和∑TUs1.8,不同重金属毒性效应顺序为CrCdPbAsHg. 相似文献
280.
为确定某ABS树脂装置丁二烯聚合工段废水水质,特别是特征有机物种类,采用吹扫捕集、静态顶空、固相萃取、固相微萃取和液液萃取等预处理方法与GC/MS(气相色谱/质谱)联用,定性检测出该工段废水中含有16种挥发、半挥发性有机物,主要包括烯烃、苯系物、有机腈、多环芳烃、醚、醇和胺. 废水ρ(SS)(SS为悬浮物)为540.31 mg/L;SS粒径主要分布在0.10~5.00 μm之间,可吸附水中4.83%~33.21%的对二甲苯、乙苯、苯乙烯和1,5-环辛二烯等有机物. 与生活污水不同,该工段废水三维荧光光谱图的荧光区域集中在λEx/λEm(激发波长/发射波长)=205~285 nm/310~360 nm范围内,主要包括λEx/λEm为285 nm/350 nm、260 nm/310 nm、225 nm/345 nm、210 nm/315 nm、230 nm/360 nm的5个荧光峰,由甲苯、靛蓝、苯乙烯、脱氢松香酸、芴、菲等苯系物和多环芳烃类有机物引起. 废水在200~250 nm之间有较强紫外吸收峰,主要由1,3-丁二烯、苯甲醛、苯乙酮、4-苯基-1-环己烯等共轭二烯、不饱和醛、酮和苯系物等有机物引起. 相似文献