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11.
在相山铀矿床田东部地区,采用同位素技术和放射性水化学技术,对铀矿床地下水放射性污染问题从理论实践两方面方面进行研究,获得了当地雨水线的线性回归方程和在铀矿床的勘探开采过程中不会造成明显的地下水放射性污染的结论 相似文献
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Recent Environmental Change and Atmospheric Contamination on Svalbard as Recorded in Lake Sediments – an Introduction 总被引:1,自引:1,他引:1
This paper outlines an interdisciplinary project on recent environmental change and atmospheric contamination on the high Arctic archipelago of Svalbard (76°30′N–80°30′N). It describes the rationale and aims of the project and summarises the location, climate, geology, vegetation, and land-use of Svalbard. 相似文献
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Heavy metal concentrations were investigated in overbank sediments of the Mala Panew River, southern Poland. Samples were collected from seven vertical profiles located within channel infills of a 20th century floodplain at three sites, each up to 50 m wide. In each profile, 15–24 samples were collected and analysed for Ba, Cd, Cu, Pb, and Zn. Sequential extraction of these elements was carried out in the 0.063-mm fraction of selected samples. Additionally, the age of the oldest trees growing close to the profiles has been used to estimate the initiation of sediment accumulation there. Ba, Cu, and Pb, which occur mostly in less mobile, moderately reducible, and residual fractions, were used for sediment dating. Zn and Cd, which in 50–75% occur in the mobile exchangeable fraction, were not suitable for dating. Correlation of Ba, Cu, and Pb concentrations in vertical profiles with changes in the load of effluents discharged to the river showed abrupt changes in the thickness of the strongly polluted sediments across the floodplains. A comparison of the relative changes between heavy metal peaks in sediments of similar age in the different profiles suggests a variable rate of downward metal migration. In general, none of the heavy metals investigated seems to have been mobilised within the stratigraphic layers above the water table. In layers located at stratigraphically lower levels, the Zn and Cd peaks seem to migrate several centimetres to several decimetres down in the profile. In profiles inundated for several weeks every year, Zn and Cd, as well as the relatively less mobile Ba, Cu, and Pb, have migrated downward by several decimetres. The investigation shows that frequent fluctuations of the water table have blurred the original depositional metal patterns of metal concentrations within a period of less than 40 years. 相似文献
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In this study, the impact of geothermal water on ground and surface waters has been investigated in Akarcay Basin, Turkey. The release of thermal return water from district heating in the city of Afyon and from thermal baths has a considerable environmental impact on the main stream. Historical analyses of stream water quality data show that the present pollution is associated primarily with thermal return water of district heating system. Currently, about 6% of stream water comprises of thermal water. The pollution seems to degrade the water quality in Lake Eber. Streambed sediments were found to be in equilibrium with polluted water and may lead to additional pollution in lake water. Thermal groundwater intrusion to fresh water production wells was detected mainly at sites close to geothermal fields. Solutions to remove thermal water from surface environment are suggested. 相似文献
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本文应用污染指数法,对北方某经济开发区及周边地下水水质进行了污染评价,结果表明研究区地下水水质以轻污染和中污染为主,局部地区出现较重污染,主要指标为硝酸盐氮、三氯甲烷和三氯乙烯。通过对工业废水、再生水、河水水质的检测,发现研究区地表水水质与污水处理厂再生水排放密切相关,地下水污染很可能与开发区企业排污有关。由于开发区所处位置的环境敏感性和脆弱性,建议今后在开发区及附近继续开展相关研究,进一步查明地下水的硝酸盐氮及有机污染物来源、污染途径,建立完善的监测体系,以便及时切断污染源,保障城市及当地供水安全。 相似文献
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为了探讨广东雷州珍稀海洋生物国家级自然保护区海域水体和沉积物中石油类的含量及其分布特征,文章于2017年和2018年分别对保护区海域的石油类进行了调查。结果表明,保护区表层水体石油类含量为0.003~0.066mg/L,平均含量为0.015mg/L,平均污染指数为0.30,保护区水体中的石油类基本符合一类海水水质标准。保护区表层沉积物中石油类含量为3.0~54.8mg/kg,平均值为11.109mg/kg,符合海洋沉积物第一类质量标准。保护区水体和沉积物中石油类含量的变化规律基本相似,但是沉积物中石油类含量的变化更大。根据调查数据分析,保护区水体中石油类的主要来源是保护区社区小型渔船航行排放的石油类,以及保护区周边渔船在航行过程排放的石油类扩散到保护区海域。 相似文献
18.
文章通过钦州湾现场调查资料,分别利用单因子污染指数法和富营养化指数法对湾内水质的污染状况和富营养化水平进行评价,并分析讨论不同的富营养化水平条件下浮游植物叶绿素a的响应。结果显示,钦州湾的污染状况和富营养化程度从湾顶至湾外呈现由重至轻的梯度变化,并出现两个“极端区域”:茅尾海化学需氧量(COD)和营养盐的污染指数劣于三类海水水质标准并重度富营养化;外湾污染指数符合一类海水水质标准并贫营养化。分析表明,茅尾海的重度富营养化是由河流输入、相对封闭的地形以及过度的牡蛎养殖造成,而外湾的贫营养化则主要归因于较少的水产养殖和陆源污水排放以及大量的浮游植物对磷酸盐的消耗。叶绿素a在这两个区域均呈现低值,茅尾海内主要是由于贝类滤食大粒径浮游植物和真光层深度下降引起,而外湾则是氮磷比(N/P)失衡,浮游植物生长受磷限制导致。另外,核电站温排水有可能是导致叶绿素a较高的原因。减少茅尾海内的养殖规模,种植红树林,集中污水于外湾排放,加强温排水口的水质监控是保证钦州湾海洋生态环境可持续发展的手段。 相似文献
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G. A. Herbert R. C. Schnell H. A. Bridgman B. A. Bodhaine S. J. Oltmans G. E. Shaw 《Journal of Atmospheric Chemistry》1989,9(1-3):17-48
The second Arctic Gas and Aerosol Sampling Program (AGASP-II) was conducted across the Alaskan and Canadian Arctic in April 1986, to study the in situ aerosol, and the chemical and optical properties of Arctic haze. The NOAA WP-3D aircraft, with special instrumentation added, made six flights during AGASP-II. Measurements of wind, pressure, temperature, ozone, water vapor, condensation nuclei (CN) concentration, and aerosol scattering extinction (bsp) were used to determine the location of significant haze layers. The measurements made on the first three flights, over the Arctic Ocean north of Barrow and over the Beaufort Sea north of Barter Island, Alaska are discussed in detail in this report of the first phase of AGASP II. In the Alaskan Arctic the WP-3D detected a large and persistent region of haze between 960 and 750 mb, in a thermally stable layer, on 2, 8, and 9 April 1986. At its most dense, the haze contained CN concentrations >10,000 cm–3 and bsp of 80×10–6 m–1 suggesting active SO2 to H2SO4 gas-to-particle conversion. Calculations based upon observed SO2 concentrations and ambient relative humidities suggest that 104–105 small H2SO4 droplets could have been produced in the haze layers. High concentrations of sub-micron H2SO4 droplets were collected in haze. Ozone concentrations were 5–10 ppb higher in the haze layers than in the surrounding troposphere. Outside the regions of haze, CN concentrations ranged from 100 to 400 cm–3 and bsp values were about (20–40)×10–6 m–1. Air mass trajectories were computed to depict the air flow upwind of regions in which haze was observed. In two cases the back trajectories and ground measurements suggested the source to be in central Europe. 相似文献