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241.
The City of Cedar Rapids obtains its municipal water supply from four well fields in an alluvial aquifer along the Cedar River in east-central Iowa. Since 1992, the City and the U.S. Geological Survey have cooperatively studied the groundwater-flow system and water chemistry near the well fields. The geochemistry in the alluvial aquifer near the Seminole Well Field was assessed to identify potentially reactive minerals and possible chemical reactions that produce observed changes in water chemistry. Calcite, dolomite, ferrihydrite, quartz, rhodochrosite, and siderite were identified as potentially reactive minerals by calculating saturation indexes. Aluminosiicate minerals including albite, Ca-montmorillonite, gibbsite, illite, K-feldspar, and kaolinite were identified as potentially reactive minerals using hypothetical saturation indexes calculated with an assumed dissolved aluminum concentration of 1 microgram per liter. Balanced chemical equations derived from inverse-modeling techniques were used to assess chemical reactions as precipitation percolates to the water table. Calcite dissolution was predominate, but aluminosilicate weathering, cation exchange, and redox reactions also likely occurred. Microbial-catalyzed redox reactions altered the chemical composition of water infiltrating from the Cedar River into the alluvial aquifer by consuming dissolved oxygen, reducing nitrate, and increasing dissolved iron and manganese concentrations. Nitrate reduction only occurred in relatively shallow (3 to 7 meters below land surface) groundwater near the Cedar River and did not occur in water infiltrating to deeper zones of the alluvial aquifer.  相似文献   
242.
用分子地球化学方法监测青岛海藻中痕量的油品污染   总被引:1,自引:0,他引:1  
两种海藻采自山东青岛太平角及汇泉角,在研究其化学组成的过程中发现,抽提物饱和烃馏份中的生物标志化合物面貌具有成熟原油的特征,它们的成熟度参数C29甾20S/(20S 20R)值达0.51,细菌生源的藿烷类化合物m/z191的强度,比生源为藻类等有机质的甾烷类化合物m/z217的强度高出约—个数量级,并且存在成岩过程的热演化产物重排甾烷,这些都不是所分析的两种现代生物藻所应具有的生物标志物面貌,而是某一种成熟原油的面貌。经将样品加热模拟实验后,进一步证实山东省青岛太平角及汇泉角的海藻可能已遭现代油品的痕量污染。  相似文献   
243.
国外尾矿酸性排水和重金属淋滤作用研究进展   总被引:1,自引:0,他引:1  
尾矿引起的环境问题是水 气 矿物在地表条件下发生复杂反应的综合结果。近年来 ,国外学者研究显示 ,发生在尾矿中的风化作用不仅仅有硫化物的氧化作用 ,而且还伴随有机物氧化作用 ,碳酸盐等矿物中和作用 ,次生矿物沉淀作用、结晶作用、胶结作用 ,矿物交代蚀变作用、吸附作用、离子交换作用以及生物作用。上述各种作用互相影响 ,互相制约。目前 ,最新研究表明 ,许多因素都会影响尾矿风化作用 ,这些因素主要包括 :尾矿原生矿物组成、成因、化学成分、表面积和形态 ;尾矿酸中和潜力 ;溶液pH值 ;次生矿物形成及其吸附、离子交换、胶结作用 ;溶液中Fe3+离子的浓度 ;有机物的种类和含量 ;尾矿粒度分布和空隙度 ;气候条件和尾矿的水文地质环境  相似文献   
244.
环境地球化学污染元素的参数评估法及环境评价   总被引:2,自引:0,他引:2       下载免费PDF全文
环境污染中的无机污染在很大程度上需要判断是否污染及污染的程度.笔者用常规地球化学方法对数据处理后,用t-分布检验是否具区域性污染,用分级指数判别其污染的程度,结果表明用简单的地球化学方法可以解决环境的基本问题.   相似文献   
245.
ABSTRACT: Migration of plutonium, americium, and uranium (actinides) in the environment at the Rocky Flats Environmental Technology Site (RFETS) is the subject of ongoing studies to develop effective strategies for cleanup and regulatory closure of the Department of Energy facility. The Actinide Migration Evaluation pathway analysis quantified actinide transport processes to validate a qualitative conceptual model of environmental actinide transport. Major actinide transport mechanisms evaluated include surface water, ground water, airborne, and biological pathways. Relative quantities of actinide movement via different pathways were compared in terms of actinide loads delivered off the RFETS, using a combination of monitoring data, predictive transport models and results from historic RFETS studies. Results indicate air and surface water constitute the dominant transport mechanisms for plutonium and americium. In ground water, shallow alluvial flow is a limited pathway for plutonium and americium because of the low aqueous solubility of these actinides and their tendency to sorb to soil. However, localized flow in shallow alluvium is a more significant pathway for uranium movement, because of the relatively higher solubility of uranium (VI) species, though isotopic ratios indicate much of the uranium is from natural sources. Biological transport of actinides by mammals, birds, fish, and arthropods is small compared to the other pathways.  相似文献   
246.
本文提出一种研究区域环境地球化学解决宏观环境问题的新思路,按照环境—地球化学—地质构造三对应的原则提出“八五”后期、“九五”和2000年后区域环境地球化学分阶段发展的设想。除了为国家提供保护治理环境的决策依据外,区域环境地球化学在理论上需要建立起地质地球化学—生态系统物质大循环模型,进行典型环境元素全球对比研究。  相似文献   
247.
ABSTRACT: Water samples collected from 14 underground coal mines in Colorado were analyzed for major dissolved constituents. The data indicate the water quality of 13 of the samples has developed by the interaction of calcite saturated ground water with sodium rich marine shales. Those samples that displayed evidence of being most completely reacted were composed almost entirely of sodium and bicarbonate ions and had a calcium to sodium activity ratio of 0.16, similar to that of seawater. The one sample that was not saturated with respect to calcite was saturated with respect to gypsum. The dissolved solids concentration attainable by dissolution of gypsum is much less than that attainable by the calcite marine shale equilibration, or approximately 2,500 milligrams per liter. By considering the maximum predicted concentrations of dissolved solids in relation to promulgated water quality criteria, it is possible to predict the hazards of reuse of this mine drainage. The primary problems would be damage or destruction of crops if the drainage water was used for irrigation. In addition, some samples contained concentrations of chloride and sulfate in excess of recommended standards for public water supplies.  相似文献   
248.
为摸清土壤氟异常对生态环境的影响,利用贵州省多目标区域地球化学调查(1:250 000)项目成果,对贵阳中心区土壤氟的地球化学特征进行了深入研究,并采用全氟指数法对土壤环境质量及其生态环境效应进行初步评价.结果表明:①贵阳中心区土壤氟含量较高,表层、深层土壤氟含量平均值分别为1 143、1 438 mg/kg,且空间分布变化较大;氟含量随土层深度的增加而升高. ②不同类型土壤中氟含量变化较大,其中紫色土中含量(1 306 mg/kg)最高,水稻土次之,石灰土、粗骨土、黄壤等差别较小,其含量范围在1 099~1 167 mg/kg之间. ③土壤氟含量与其母岩呈显著正相关性,且土壤中氟含量较母岩更高,表明风化成土过程中存在一定富集,土壤氟与成土母岩之间具有一定继承性. ④土壤氟环境质量评价结果表明,研究区土壤存在局部氟污染(异常),污染区、警戒区、安全区和清洁区所占比例分别为13.6%、62.2%、19.2%和5.0%. ⑤生态环境效应初步调查结果显示,局部土壤受氟污染区的油菜和稻谷样品中氟含量范围分别为1.86~2.68和10.40~13.50 mg/kg,同时地下水也受到一定程度的氟污染.因此,贵阳中心区土壤氟含量较高,局部土壤已受到氟污染,可能会对农产品质量、饮水安全及人体健康产生一定影响,建议政府部门及科研工作者予以高度重视.   相似文献   
249.
ABSTRACT: Ground water samples were collected from 30 wells located in, or directly down gradient from, recharge areas of the Eutaw aquifer in Montgomery, Alabama. The major ion content of the water evolves from calcium‐sodium‐chloride‐dominated type in the recharge area to calcium‐bicarbonate‐dominated type in the confined portion of the aquifer. Ground water in the recharge area was under saturated with respect to aluminosilicate and carbonate minerals. Ground water in the confined portion of the aquifer was at equilibrium levels for calcite and potassium feldspar. Dissolved oxygen and nitrite‐plus‐nitrate concentrations decreased as ground water age increased; pH, iron, and sulfate concentrations increased as ground water age increased. Aluminum, copper, and zinc concentrations decreased as ground water age and pH increased. These relations indicate that nitrate, aluminum, copper, and zinc are removed from solution as water moves from recharge areas to the confined areas of the Eutaw aquifer. The natural evolution of ground water quality, which typically increases the pH and decreases the dissolved oxygen content, may be an important limiting factor to the migration of nitrogen based compounds and metals.  相似文献   
250.
The chemistry, mineralogy and morphology of two soil profiles developed on till material of granitic and gneissic composition in south-western Sweden were studied in relation to podzolization processes. These soils were used for treatments with lime and wood ash. The profiles do not show characteristic Podzol morphology but qualify as Spodosols under Soil Taxonomy criteria and are probably typical for the coniferous forest soils of south-western Sweden. Podzolization features are clear but less well expressed than in classic Podzols. The distribution of major elements shows podzolization features with accumulation of sesquioxides in the B horizons and depletion in the eluvial horizons. Quartz and feldspars dominate the bulk soils reflecting the clear relationship between the composition of the soil and the underlying bedrock. Low amounts of clay contain an interlayered vermiculitic phase as the main phyllosilicate in which the degree of interlayering, known to be pH dependent, varies with depth and is at a maximum in the Bhs horizon. In the B horizons there are small but significant amounts of imogolite-type material which affect the adsorption of sulphate.  相似文献   
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