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291.
介绍了江苏省重污染天气监测预报预警系统以及大气重污染预警会商流程,将2015年13个地级市的模式预报、人工预报结果分别与实际观测值进行比较。结果表明:人工预报更准确,PM_(2.5)日均值、臭氧日最大8 h平均值、AQI 3个指标人工预报和实况的相关性分别比模式预报高出12.8%、0.3%、11.4%,平均标准误差(MNE)分别低20.7%、3.1%、23.1%。依据国家空气质量预报技术指南评分办法,对各市2015年全年空气质量级别为"良"时进行评分。通过开展07∶00预报更新,使2015年上半年空气质量预报级别得分平均提高了0.9分,全年级别得分平均提高了2.6分;通过改进模式预报参数,使PM_(2.5)日均预报值、臭氧日最大8 h平均预报值、AQI预报值和实际观测值的相关性比上年同期分别提高26.0%、5.0%、33.9%,MNE分别降低3.6%、31.3%、7.6%。 相似文献
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Shu-Fen Cheng Chi-Ying Lai Sheng-Jie Lin Chin-Yuan Huang 《Environmental monitoring and assessment》2014,186(1):375-382
Air-drying and oven-drying are pretreatment processes often used before testing and analyzing various soil characteristics in the laboratory. This study selected three kinds of soil, including red soil, entisol, and alluvial soil, and examined the variation of the Cr(VI) content and Cr bond forms in these soils during air-drying and oven-drying. The results show that when the soil is air-dried in natural environment, the Cr(VI) content decreases with air-drying time. On day 10 of air-drying, the Cr(VI) content in these soils is 22.8~47.9 % of the initial value. When the soil is oven-dried, the Cr(VI) concentration decays faster; on day 8, the Cr(VI) is no longer detected in these soil samples. When the Cr(VI)-contaminated soil is treated by air-drying and oven-drying, the Cr bond form converts into a more stable form. After oven-drying, the Cr mainly exists in Fe–Mn oxide form, organic bond form, and residual form. The air-drying and oven-drying pretreatment processes of soil reduce the Cr(VI) content and stabilize the Cr bond form. If the laboratory analytic results are applied to risk analysis or remediation strategy planning for chromium-contaminated soil, the toxicity, bioavailability, and mobility of Cr in soil may be underrated. 相似文献
295.
依据建设项目竣工环境保护验收中污水监测的要求,通过积累大量验收监测质量检查的实验数据,运用数理统计的方法,以化学需氧量和氨氮两个项目为例,建立了质控数据的评价方法,并确定了现场平行样偏差指标的限値。 相似文献
296.
采用改性沸石分离富集-火焰原子吸收光谱法测定长江水中微量镉,优化了富集和洗脱条件,讨论了干扰离子的影响。方法在0μg~4.00μg范围内线性良好,检出限为0.214μg/L,长江水平行测定的RSD为1.8%,加标回收率为99.0%~104%。 相似文献
297.
Zhou L Li H Yu Z Ren M Zeng X Peng P Sheng G Fu J 《Journal of environmental monitoring : JEM》2012,14(7):1935-1942
Polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polybrominated dibenzo-p-dioxins and dibenzofurans (PBDD/Fs) in surface sediment samples from Taihu Lake--an important water supply of the Yangtze River Delta, China--were investigated in the present study. Concentrations of PCDD/Fs ranged from 0.91 to 4.8 pg TEQ g(-1) dw (mean: 2.9 pg TEQ g(-1) dw, TEQ: Toxic Equivalent), which were all higher than the threshold effect level established by interim sediment quality guidelines in Canada (0.85 pg TEQ g(-1) dw). The levels of PBDD/Fs ranged from 0.16 to 1.6 pg TEQ g(-1) dw (mean: 0.52 pg TEQ g(-1) dw) and accounted for 5-33% (mean: 14%) of the total PCDD/Fs and PBDD/Fs TEQ. Comparatively, the abundance of sedimentary PCDD/Fs in the three regions (Meiliang Bay, Gonghu Bay, and Xukou Bay) showed a decreasing trend from the inflow region to the outflow region, while no significant difference was observed among their 2,3,7,8-PBDD/Fs levels, which suggested that the sources of PCDD/Fs and PBDD/Fs differed in this area. Principal component analysis suggested that the historical production/usage of pentachlorophenol and sodium pentachlorophenate was the dominant source of PCDD/Fs in the sediment of these regions. Although the specific sources of PBDD/Fs in the sediment of Taihu Lake were unclear, it was suspected to be due to atmospheric deposition; however, an additional study is needed to confirm this. 相似文献
298.
Locating pollutant emission sources with optical remote sensing measurements and an improved one-dimensional radial plume mapping technique 总被引:1,自引:0,他引:1
Previous studies have shown that there was a relatively large amount of uncertainty along the major wind direction in the results of locating emission sources using the one-dimensional radial plume mapping (RPM(1D)) technique based on optical remote sensing measurements. This paper proposes setting up an additional monitoring line that is perpendicular to the original scanning beam geometry to reduce this uncertainty. We first conducted a computer simulation study using the Gaussian dispersion model to generate the downwind concentrations of plumes from 400 source locations in a 201 m × 201 m spatial domain under various wind directions (n = 181). The optical remote sensing instrument was assumed to be at (0, 0) with two perpendicular monitoring lines, each of which had three beam segments of equal length. Each pair of the reconstructed downwind concentration profiles was then used to trace back to the source locations. The results showed that the accuracy of the method and its uncertainty were improved by using the proposed two-line RPM(1D) approach rather than the original one-line RPM(1D) approach at most simulated source locations. In a follow-up field experiment, a tracer gas was released at the coordinate of (100, 100). The release location was covered within the 0.25- to 0.5-probability area of the estimated results, and the distance between the actual and estimated source locations was 18.4 m (9.2% of the longest beam path). 相似文献
299.
挥发性有机物污染土壤样品采样方法比较 总被引:1,自引:0,他引:1
以苯系物污染土壤样品的采集为例,比较了4种不同采样方法导致样品检测结果的差异。其中,方法 1将样品装填至广口瓶内并压实密封,方法2采用非扰动采样器采集10 g样品后转移至加有10 mL甲醇保护剂的Vial瓶中密封,方法 3用非扰动采样器采集10 g样品后直接将其密封于采样器内,方法 4用Encore采样器采样后将其密封于采样器内。结果表明,方法 2采集样品的检出率最高,其余3种方法的差异不明显,方法 2采集样品的检出结果 71%以上都大于其余3种方法。而且,对于挥发性较强的苯与甲苯,以方法 2采集的样品91%以上都大于其余3种方法,最大及平均检出浓度高出2~3个数量级。5种不同土质样品检测结果表明,对于有机质含量较低的细砂,方法2的最高及平均检出浓度均高于其余3种方法 1~3个数量级,差异随土壤有机质含量的升高而降低。可见,对于苯系物及挥发性强于苯系物的其他挥发性有机物污染土壤样品的采集,方法 2效果最优,可指定为VOCs污染场地土壤样品的采样方法。 相似文献
300.