全文获取类型
收费全文 | 17677篇 |
免费 | 293篇 |
国内免费 | 388篇 |
专业分类
安全科学 | 630篇 |
废物处理 | 743篇 |
环保管理 | 2632篇 |
综合类 | 2999篇 |
基础理论 | 4550篇 |
环境理论 | 7篇 |
污染及防治 | 4638篇 |
评价与监测 | 1003篇 |
社会与环境 | 1029篇 |
灾害及防治 | 127篇 |
出版年
2023年 | 99篇 |
2022年 | 172篇 |
2021年 | 170篇 |
2020年 | 197篇 |
2019年 | 160篇 |
2018年 | 296篇 |
2017年 | 278篇 |
2016年 | 436篇 |
2015年 | 345篇 |
2014年 | 452篇 |
2013年 | 1429篇 |
2012年 | 625篇 |
2011年 | 899篇 |
2010年 | 677篇 |
2009年 | 768篇 |
2008年 | 835篇 |
2007年 | 875篇 |
2006年 | 724篇 |
2005年 | 609篇 |
2004年 | 629篇 |
2003年 | 569篇 |
2002年 | 542篇 |
2001年 | 645篇 |
2000年 | 521篇 |
1999年 | 316篇 |
1998年 | 209篇 |
1997年 | 232篇 |
1996年 | 222篇 |
1995年 | 266篇 |
1994年 | 212篇 |
1993年 | 209篇 |
1992年 | 174篇 |
1991年 | 182篇 |
1990年 | 179篇 |
1989年 | 180篇 |
1988年 | 153篇 |
1987年 | 133篇 |
1986年 | 156篇 |
1985年 | 143篇 |
1984年 | 190篇 |
1983年 | 147篇 |
1982年 | 171篇 |
1981年 | 157篇 |
1980年 | 130篇 |
1979年 | 149篇 |
1978年 | 94篇 |
1977年 | 98篇 |
1975年 | 88篇 |
1974年 | 93篇 |
1972年 | 96篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
201.
In FRG and other countries unequivocal criteria for the limitation of dioxins (PCDD's/PCDF's) in food like vegetables and fruits are lacking. These have to be directly associated with the limitation of dioxins in the soil and the deposition of particulate matter as the two main pathways for plant contamination. Based on recent investigations in the vicinity of cable-waste incinerators in Northrhine-Westphalia with comparatively high contents of dioxins in garden plants and soils and other sources of dioxins, considerations are given for the establishment of the criteria urgently needed. 相似文献
202.
F. A. Norris J. W. Noling R. L. Jones S. D. Kirkland A. J. Overman C. D. Stanley 《Journal of contaminant hydrology》1991,8(3-4)
Unsaturated- and saturated-zone field studies were conducted under two different agricultural conditions in Florida, U.S.A., to measure the movement and degradation of ethoprop.When ethoprop was applied to a sand soil in an orange grove located on the Florida central ridge, soil residues declined with a half-life of 13 days to near the limit of detection (0.01 μg g−1 within 2 months. Ethoprop residues were generally contained in the upper 2 m of soil. Although low levels of ethoprop were found in four groundwater samples within the first 3 months after application, the cause of these isolated and transient residues could not be determined. The data show that there was no widespread plume of ethoprop residues beneath or downgradient from the treated area.On a flatwood soil on the west coast of Florida, ethoprop was incorporated into raised beds and protected by a plastic mulch in which tomatoes were grown. When the plastic mulch was present, ethoprop soil residues declined with a half-life of 40 days and were confined to the upper 0.3 m of soil. After the mulch was removed at crop harvest, the remaining ethoprop dissipated with a half-life of 12 days. Groundwater residues in excess of 1 μg L−1 were confined to a single sample collected after the well had been damaged during a rototilling operation. Resides of < 1 μg L−1 were present in three later samples from this well. At the sampling interval where the highest residues were detected in the damaged well, ethoprop residues of < 1 μg L−1 were also found in three other wells but no residues were detected in these wells in later samples. 相似文献
203.
204.
This paper explores the relationship between the toxicity of certain organic pollutants and their tissue concentration and suggests that the latter may be a more accurate predictor of toxicity than exposure concentration. 相似文献
205.
The concept of “Environmental Hazard Profile” developed at this institute has been tested with 100 14C-labelled organic compounds. Concentration factors in activated sludge, in algae and fish were determined. The microbial degradation of the chemicals to CO2 in activated sludge and the decomposition to CO2 under artificial light were determined. Ranking of compounds is given in the order of falling concentration factors and accumulation in rats respectively, and decreasing rates of decomposition. Relationship between chemical structure and accumulative and degradative behaviours is demonstrated using some selected groups of chemicals, such as benzenes, phenols, biphenyls and polyaromatic hydrocarbons. Correlations between the octanol/water partition coefficient, concentration factors and rates of decomposition could be established. Evaluation of test compounds was possible using hazard profiles obtained by the sum of single test results. 相似文献
206.
Gas phase benzyne generated from the high temperature pyrolysis of phthalic anhydride is reduced to benzene. This newly formed benzene is then free to react further with more benzyne to yield more complex aromatic hydrocarbons. 相似文献
207.
Koh CH Khim JS Villeneuve DL Kannan K Giesy JP 《Environmental pollution (Barking, Essex : 1987)》2006,142(1):48-57
This study employed mechanism-specific in vitro bioassays to help characterize the occurrence and distribution of dioxin-like and estrogenic contaminants in sediment from Yeongil Bay, Korea. Approximately 85% of the sediments tested induced significant dioxin-like activity in the H4IIE-luc bioassay, while approximately 50% induced significant estrogenic activity in the MVLN bioassay. Instrumentally-derived estimates of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 17beta-estradiol equivalents tended to underestimate the magnitude of response observed in the bioassays, suggesting that compounds detected by chemical analysis did not account for all the activity associated with Yeongil Bay sediments, or that non-additive interactions were occurring. The greatest dioxin-like and estrogenic activity was associated with the mid-polarity Florisil fractions (F2) expected to contain polycyclic aromatic hydrocarbons (PAHs) as well as chlorinated dioxins and furans. As in previous studies of Korean coastal sediment, more polar fractions (F3) generated more modest responses both in terms of magnitude and the number of samples responding. 相似文献
208.
Melamine-based organoclay to sequester atrazine 总被引:4,自引:0,他引:4
Sequestration of aqueous atrazine by organoclays prepared from the surfactant 6-piperazin-1-yl-N,N'-bis-(1,1,3,3-tetramethyl-butyl)-(1,3,5)triazine-2,4-diamine and Gonzales bentonite was assessed using 14C-labeled atrazine. Organoclays with varying ratios of surfactant to clay were evaluated with respect to their ability to sequester atrazine from an aqueous solution. Organoclays containing 100-200 g kg-1 surfactant on a total weight basis provided the most efficient adsorption of atrazine, with apparent KOC values exceeding 5000 l kg-1 at these loading fractions. Less than 12% of sequestered atrazine was released during four sequential day long washings, supporting our expectation that the majority of the reaction of atrazine with the surfactant lead to irreversible chemical bond formation through nucleophilic aromatic substitution. 相似文献
209.
Araújo CV Cohin-de-Pinho SJ da S Santos J Delgado F Santana LC Chastinet CB da Silva EM 《Chemosphere》2006,65(4):599-603
The suitability and viability of acute in situ bioassays were investigated in the biomonitoring program of an acidic lake contaminated with sulphur residues. Responses of organisms observed in laboratory and in situ bioassays were also assessed to determine whether or not they were similar and comparable, regarding accuracy and precision. Newborn Poecilia reticulata were employed as test organisms and exposed to the same water samples under in situ and laboratory conditions. Mortality/immobility was the endpoint assessed and dead/immobile organisms were counted at various time intervals during exposure. The mean calculated LT50 values and 95% confidence intervals were 1.61 (1.36-1.87) h in the laboratory bioassays and 0.72 (0.55-0.89) h in the in situ bioassays. Statistical comparison of these values revealed a significant difference (p<0.05). In situ bioassays were more accurate than those carried out in the laboratory, demonstrating higher sensitivity and better reproduction of what occurs in nature, while laboratory bioassays were more precise. 相似文献
210.
This work has been the first application of DGT samplers for measuring metals in water and sediment porewater in the Antarctic environment, and whilst DGT water sampling was restricted to quantification of Cd, Fe and Ni, preconcentration using Empore chelating disks provided results for an additional nine elements (Sn, Pb, Al, Cr, Mn, Co, Cu, Zn, As). Although higher concentrations were measured for some metals (Cd, Ni, Pb) using the Empore technique, most likely due to particulate-bound or colloidal species becoming entrapped in the Empore chelating disks, heavy metal concentrations in the impacted Brown Bay were found to be comparable with the non-impacted O'Brien Bay. Sediment porewater sampling using DGT also indicated little difference between Brown Bay and O'Brien Bay for many metals (Cd, Al, Cr, Co, Ni, Cu), however, greater amounts of Pb, Mn, Fe and As were accumulated in DGT probes deployed in Brown Bay compared with O'Brien Bay, and a higher accumulation of Sn was observed in Brown Bay inner than any of the other three sites sampled. Comparison of DGT derived porewater concentrations with actual porewater concentrations showed limited resupply of Cd, Pb, Al, Cr, Mn, Co, Ni, Cu, Zn and As from the solid phase to porewater, with these metals appearing to be strongly bound to the sediment, however, resupply of Fe and Sn was apparent. Based upon our observations here, we suggest that Sn, and to a lesser extent Pb, are critical contaminants. 相似文献