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11.
Changes in air pollutants during the COVID-19 lockdown in Beijing:Insights from a machine-learning technique and implications for future control policy
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Jiabao Hu Yuepeng Pan Yuexin He Xiyuan Chi Qianqian Zhang Tao Song Weishou Shen 《大气和海洋科学快报》2021,14(4):63-69
基于2015-2020年北京35个环境空气站和20个气象站观测资料,应用机器学习方法(随机森林算法)分离了气象条件和源排放对大气污染物浓度的影响.结果发现,为应对疫情采取的隔离措施使北京2020年春节期间大气污染物浓度降低了35.1%-51.8%;其中,背景站氮氧化物和一氧化碳浓度的降幅最大,超过了以往报道较多的交通站... 相似文献
12.
根据保守污染物的迁移、转化特点,提出保守污染物水环境容量计算方法,并将这种方法应用于大辽河流域,得到地表水环境质量标准(GB3838-2002)中规定的各种保守污染物的水环境容量,为流域保守污染物水环境容量总量控制提供了一种技术方法。 相似文献
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PRESENT STATUS OF EXPERIMENTAL STUDY ON HEAVY METAL POLLUTANT ADSORPTION-DESORPTION BY SEDIMENT IN CHINA 总被引:1,自引:0,他引:1
PRESENTSTATUSOFEXPERIMENTALSTUDYONHEAVYMETALPOLLUTANTADSORPTION-DESORPTIONBYSEDIMENTINCHINAHUANGSuiliangandWANZhaohui(Postdoc... 相似文献
17.
Lead analysis of sediment cores from seven Connecticut lakes 总被引:2,自引:0,他引:2
Lead analyses were performed on sediment cores from seven Connecticut lakes by dilute acid leaching. The absolute concentrations of lead varied from core to core, but the lead profiles were similar in all of the cores, and each depicted a point where the concentration of lead sharply increased above background levels. The background lead concentrations observed in the bottom portions of the cores ranged from 12-54 g Pb/g sediment with a mean of 30 g Pb/g, and increased to a mean maximum of 310 g Pb/g. In six of the lakes significant increases above background levels were not noted until between 1924 and 1952, suggesting that, at least for Connecticut lakes, the point in a lake sediment core where the concentration of lead began to increase was after ca. 1924, and on average about 1930. Lead concentrations declined in the surface sediments of only three of the lakes, mostly since the 1980's, and presumably in response to the phasing out of leaded gasoline. However, significant declines in lead concentrations were not observed in the remaining cores, possibly due to increased motor vehicle use within the airshed of the lakes and/or changes in the export of lead to the lakes from their watersheds. 相似文献
18.
ABSTRACTWidespread forest fire events occurred in the foothills of North Western Himalaya during 24 April to 2 May 2016 (Event-1) and 20–30 May 2018 (Event-2). Their impacts were investigated on the distribution of pollutant gases ozone (O3), carbon monoxide (CO), and oxides of nitrogen (NOx) over Uttarakhand using simulations of Weather Research and Forecasting model coupled with chemistry (WRF-Chem) and in-situ observations of these gases over Dehradun, the capital of Uttarakhand. During Event-1, the observed CO mixing ratio over Dehradun increased from 25 April 2016 onwards, attained maximum (705.8 ± 258 ppbv) on 2 May 2016 and subsequently decreased. The rate of increase of daily baseline CO was 29 ppbv/day during HFAP (High Fire Activity Period). During Event-2, daily average concentrations of CO, O3, and NOx showed systematic increase over Dehradun during HFAP period. The rate of increase of CO was 9 ppbv/day, while it was very small for NOx and O3. To quantitatively estimate the influence of forest fire emissions, two WRF-Chem simulations were made: one with biomass burning (BB) emissions and other without BB emissions. These simulations showed 52% (34%) enhancement in CO, 52% (32%) enhancement in NOx, and 11% (9%) enhancement in O3 during HFAP for Event-1 (Event-2). A clear positive correlation (r = 0.89 for Event-1, r = 0.69 for Event-2) was found between ?O3 (O3with BB minus O3without BB) and ?CO (COwith BB minus COwithout BB), indicating rapid production of ozone in the fire plumes. For both the events, the vertical distribution of ?O3, ?CO, and ?NOx showed that forest fire emissions influenced the air quality upto 6.5 km altitude. Peaks in ?O3, ?CO, and ?NOx during different days suggested the role of varying dispersion and horizontal mixing of fire plumes. 相似文献
19.
ABSTRACTRapid economic growth, a high degree of urbanization and the proximity of a large number of desert and semidesert landscapes can have a significant impact on the atmosphere of adjacent territories, leading to high levels of atmospheric pollution. Therefore, identifying possible sources of atmospheric pollution is one of the main tasks. In this study, we carried out an analysis of spatial and temporal characteristics of five main atmospheric pollutants (PM2.5, PM10, SO2, NO2, and CO) near potential source of natural aerosols, affecting seven cities (Wuhai, Alashan, Wuzhong, Zhongwei, Wuwei, Jinchang, Zhangye), located in immediate proximity to the South Gobi deserts. The results, obtained for the period from 1 January 2016 to 31 December 2018, demonstrate total concentrations of PM2.5 and PM10 are 38.2 ± 19.5 and 101 ± 80.7 μg/m3 exceeding the same established by the Chinese National Ambient Air Quality Standard (CNAAQS), being 35 and 70 μg/m3, respectively. Based on the data from Moderate Resolution Imaging Spectroradiometer (MODIS) for the whole period, Clean Сontinental (71.49%) and Mixed (22.29%) types of aerosols prevail in the region. In the spring and winter seasons maximum concentrations of pollutants and high values of Aerosol Optical Depth (AOD) in the region atmosphere are observed. PM2.5 and PM10 ratio shows the presence of coarse aerosols in the total content with value 0.43. The highest concentrations of pollutants were in the period of dust storms activity, when PM2.5 and PM10 content exceeded 200 and 1000 µg/m3, and AOD value exceeded 1. UV Aerosol Index (UVAI), Aerosol Absorbing Optical Depth (AAOD), and Single Scattering Albedo (SSA), obtained from Ozone Monitoring Instrument (OMI), demonstrate the high content of dust aerosols in the period of sandstorms. Analysis of backward trajectories shows that dust air masses moved from North to Northwest China, affecting large deserts such as Taklamakan, Gurbantunggut, Badain Jaran, Tengger, and Ulan Buh deserts. 相似文献
20.
Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in sediments from Hong Kong 总被引:4,自引:0,他引:4
Müller JF Gaus C Prange JA Päpke O Poon KF Lam MH Lam PK 《Marine pollution bulletin》2002,45(1-12):372-378
Concentrations of 2,3,7,8-substituted polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were determined in 14 sediment samples collected from four sites in the Mai Po Marshes Nature Reserve (within a RAMSAR Site) and from another six sites in Victoria Harbour and along the Hong Kong coastline. Elevated levels of PCDDs, and particularly OCDD, were detectable in all samples collected from the Mai Po Marshes and five of the six sites. In contrast to PCDDs, PCDFs were mainly found in sediment samples collected from industrial areas (Kwun Tong and To Kwa Wan) in Victoria Harbour. PCDD/F levels and congener profiles in the samples from the Mai Po Marshes Nature Reserve in particular show strong similarities to those reported in studies which have attributed similar elevated PCDD concentrations to nonanthropogenic PCDD sources. 相似文献