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71.
Oikawa S Watabe T Inatomi N Isoyama N Misonoo J Suzuki C Nakahara M Nakamura R Morizono S Fujii S Hara T Kido K 《Journal of environmental radioactivity》2011,102(3):302-310
A radioactivity survey was launched in 1991 to determine the background levels of 239+240Pu in the marine environment off a commercial spent nuclear fuel reprocessing plant before full operation of the facility. Particular attention was focused on the 240Pu/239Pu atom ratio in seawater and bottom sediment to identify the origins of Pu isotopes. The concentration of 239+240Pu was almost uniform in surface water, decreasing slowly over time. Conversely, the 239+240Pu concentration varied markedly in the bottom water and was dependent upon the sampling point, with higher concentrations of 239+240Pu observed in the bottom water sample at sampling points having greater depth. The 240Pu/239Pu atom ratio in the seawater and sediment samples was higher than that of global fallout Pu, and comparable with the data in the other sea area around Japan which has likely been affected by close-in fallout Pu originating from the Pacific Proving Grounds. The 240Pu/239Pu atom ratio in bottom sediment samples decreased with sea depth. The land-originated Pu is not considered as the reason of the increasing 239+240Pu concentration and also decreasing the 240Pu/239Pu atom ratio with sea depth, and further study is required to clarify it. 相似文献
72.
S.M. Pan S.G. TimsX.Y. Liu L.K. Fifield 《Journal of environmental radioactivity》2011,102(10):930-936
A sediment core collected from the sub-aqueous delta of the Yangtze River estuary was subjected to analyses of 137Cs and plutonium (Pu) isotopes. The 137Cs was measured using γ-spectrometry at the laboratories at the Nanjing University and Pu isotopes were determined with Accelerator Mass Spectrometry (AMS), measurements made at the Australian National University. The results show considerable structure in the depth concentration profiles of the 137Cs and 239+240Pu. The shape of the vertical 137Cs distribution in the sediment core was similar to that of the Pu. The maximum 137Cs and 239+240Pu concentrations were 16.21 ± 0.95 mBq/g and 0.716 ± 0.030 mBq/g, respectively, and appear at same depth. The average 240Pu/239Pu atom ratio was 0.238 ± 0.007 in the sediment core, slightly higher than the average global fallout value. The changes in the 240Pu/239Pu atom ratios in the sediment core indicate the presence of at least two different Pu sources, i.e., global fallout and another source, most likely close-in fallout from the Pacific Proving Grounds (PPG) in the Marshall Islands, and suggest the possibility that Pu isotopes are useful as a geochronological tool for coastal sediment studies. The 137Cs and 239+240Pu inventories were estimated to be 7100 ± 1200 Bq/m2 and 407 ± 27 Bq/m2, respectively. Approximately 40% of the 239+240Pu inventory originated from the PPG close-in fallout and about 50% has derived from land-origin global fallout transported to the estuary by the river. This study confirms that AMS is a useful tool to measure 240Pu/239Pu atom ratio and can provide valuable information on sedimentary processes in the coastal environment. 相似文献
73.
In order to measure groundwater age and design nuclear waste disposal sites, it is important to understand the sorption behavior of tritium on soils. In this study, batch tests were carried out using four soils from China: silty clays from An County and Jiangyou County in Sichuan Province, both of which could be considered candidate sites for Very Low Level Waste disposal; silty sand from Beijing; and loess from Yuci County in Shanxi Province, a typical Chinese loess region. The experimental results indicated that in these soil media, the distribution coefficient of tritium is slightly influenced by adsorption time, water/solid ratio, initial tritium specific activity, pH, and the content of humic and fulvic acids. The average distribution coefficient from all of these influencing factors was about 0.1-0.2 mL/g for the four types of soil samples. This relatively modest sorption of tritium in soils needs to be considered in fate and transport studies of tritium in the environment. 相似文献
74.
Reversed association between levels of prostate specific antigen and levels of blood cadmium and urinary cadmium 总被引:1,自引:0,他引:1
Prostate cancer associated with cadmium exposure may indicate a link between prostate specific antigen (PSA) and levels of blood cadmium (BCd) and urinary cadmium (UCd). Thus, these associations were investigated. We recruited 295 men, 50 years of age and above from a health check-up program at a health center as subjects of the study. They completed a self-reported questionnaire and provided fasting samples of blood and urine for cadmium assay. The assay was performed using atomic absorption spectrophotometry. Blood samples were also collected for the assays of total cholesterol and high-density lipoprotein measures. The means of BCd and UCd increased with age and the means of all subjects were 1.19 ± 1.04 μg L−1 and 1.37 ± 1.76 μg g−1 creatinine, respectively. The PSA levels were positively associated with the lipid levels, but reversely associated with BCd and UCd levels. The multivariate logistic regression analysis showed that men with PSA ? 4.0 ng mL−1 had an odds ratio (OR) of 0.4 (95% CI = 0.1-0.9) to have BCd > 0.49 μg L−1, and an OR of 0.4 (95% CI = 0.2-1.0) to have UCd > 0.45 μg g−1 creatinine. In conclusion, the PSA levels are reversely associated with BCd and UCd levels. 相似文献
75.
76.
不同氮磷比对多年生水生植物生长特性影响的研究 总被引:1,自引:0,他引:1
从氮、磷等植物生长的环境因子出发,研究了高低氮磷营养水平下,不同氮/磷比例的富营养化水体对聚草(Myriophyllum spicatum)、黄花水龙(Jussiaea stipulacea Ohwi)、喜旱莲子草(Alternanthera philoxeroides)生长特性的影响。结果表明,聚草在氮磷比2:1时生物量最大,且生物量在高浓度水平处理明显大于低浓度水平处理(P〈0.01);黄花水龙在氮磷比10:1~20:1时生物量最大,高低浓度水平处理问生物量无显著性差异;喜旱莲子草在较高氮磷比20:l~40:1时生物量最大,高浓度水平处理时生物量显著性高于低浓度水平处理(P〈0.05)。在低浓度水平处理时,氮为黄花水龙和喜旱莲子草生长的主要限制因子,磷为聚草生长的主要限制因子,且喜早莲子草叶绿素增长期较其他处理提前,而黄花水龙的叶绿素变化在高低营养水平下差异不显著。营养盐水平对聚草茎长和生物量的影响较对黄花水龙和喜旱莲子草的影响明显。 相似文献
77.
Shelly L. Miller Peter Scaramella Joseph Campe Cynthia W. Goss Sandra Diaz-Castillo Ed Hendrikson Carolyn DiGuiseppi Jill Litt 《Atmospheric environment (Oxford, England : 1994)》2009,43(35):5661-5667
An indoor air quality assessment was conducted on 100 homes of recent Mexican immigrants in Commerce City, Colorado, an urban industrial community north of Denver. Head of households were administered a family health survey, filled out an activity diary, and participated in a home inspection. Carbon monoxide (CO) and carbon dioxide (CO2) were measured for 24 h inside the main living area and outside of the homes. Harvard Impactors were used to collect 24-h samples of PM2.5 at the same locations for gravimetric analysis. Dust samples were collected by vacuuming carpeting and flooring at four locations within the home and analyzed by ELISA for seven allergens. Mean indoor and outdoor PM2.5 levels were 27.2 and 8.5 μg m−3, respectively. Indoor PM2.5 and CO2 were elevated in homes for which the number of hours with door/window open was zero compared to homes in which the number of hours was high (>15 h). Indoor PM2.5 levels did not correlate with outdoor levels and tended to increase with number of inhabitants, and results indicate that the source of indoor particles were occupants and their activities, excluding smoking and cooking. Mean indoor CO2 and CO levels were 1170 and 2.4 ppm, respectively. Carbon monoxide was higher than the 24-h National Ambient Air Quality Standard in 3 of the homes. The predominant allergens were cat (Fel d 1) and mouse (Mus m 1) allergens, found in 20 and 34 homes, respectively. 相似文献
78.
微曝气Fenton氧化法处理模拟双酚A废水的效果及其生物验证 总被引:2,自引:1,他引:1
研究了微曝气Fenton氧化法关键工艺参数对模拟双酚A(BPA)废水处理效果的影响,并从活性污泥性质和污染物去除率两方面,采用膜生物反应器(membrane bioreactor, MBR)对微曝气Fenton氧化法的处理效果进行了实验验证,为实现BPA废水的生物处理奠定基础。结果表明,初始pH值、反应时间、H2O2/COD(质量浓度比)、H2O2/Fe2+ (摩尔浓度比)、反应温度及曝气量均对预处理效果有较大影响,在最佳条件下,COD去除率可达70%,BOD/COD值则由原废水的0.02提高到0.50以上。MBR处理上述出水的结果表明,经微曝气Fenton氧化处理BPA的废水,可较好地适应后续的生化处理。 相似文献
79.
S.J. Sartandel S.K. Jha S.V. Bara R.M. Tripathi V.D. Puranik 《Journal of environmental radioactivity》2009,100(10):831-834
The understanding and evaluation of the possible interactions of various naturally occurring radionuclides in the world's third largest man-made dam, Nagarjuna Sagar located in Andhra Pradesh, India and built on river Krishna assumed significance with the finding of uranium deposits in locations near the dam. For the present work, surface soil samples from the mineralized area of Lambapur, Mallapuram, Peddagattu and sediment core samples from the Nagarjuna Sagar dam were analyzed for naturally occurring radionuclides namely uranium and thorium using gamma spectrometric technique. Also toxic elements lead and chromium were analysed by the Energy Dispersive X-ray Fluorescence Spectrometer (EDXRF) technique. Surface soil samples show a variation from 25 to 291 Bq/kg (2.02–23.5 mg/kg) for 238U and 32–311 Bq/kg (7.9–76.9 mg/kg) for 232Th. U/Th concentration ratio in surface soil samples ranged from 0.19 to 0.31 and was found comparable with the nation wise average of 0.26. The study of sediment core samples reflected higher U/Th concentration ratio of 0.30–0.33 in the bottom section of the core as compared to 0.22–0.25 in the upper section. The concentration ratio in the upper section of the core was similar to the ratio 0.23 found in the western Deccan Basalt region through which the river originates. A higher concentration of lead and chromium was observed in the upper section of the core compared to bottom section indicating the impact of river input on the geochemical character of dam sediment. 相似文献
80.
E. Howard Coker Rollin H. Hotchkiss Dennis A. Johnson 《Journal of the American Water Resources Association》2009,45(4):815-827
Abstract: A present and future challenge for water resources engineers is to extend the useful life of our dams and reservoirs. Ongoing reservoir sedimentation in impoundments must be addressed; sedimentation in many reservoirs already limits project benefits and effective project life. Sustainability requires that incoming sediment be moved downstream past the impounding dam. We use Lewis and Clark Lake, the most downstream of the six Missouri River main stem reservoirs, to demonstrate how a reservoir in advanced stages of its project life could be converted to a sustainable system with local benefits exceeding costs by a factor of 1.5. Full consideration of benefits would further enhance project justification. The proposed strategy involves four phases that will take about 50 years to complete. Cost estimates for this potential project range from the quantitative to the plausible, but it is clear that the results justify a full engineering, environmental, and economic study of this model project. If implemented, the project will create scientific knowledge and develop technologies useful for achieving sustainability at many other reservoirs in the Mississippi River basin and beyond. 相似文献