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41.
内蒙古敖包吐萤石矿床地质和地球化学特征   总被引:2,自引:0,他引:2  
笔者总结了敖包吐萤石矿床的地质特征,并通过萤石的稀土元素的地球化学和Nd同位素研究,探讨了该矿床的成矿作用和成矿物质来源。敖包吐萤石矿床产出于下二叠统大石寨组火山—沉积岩与燕山中期花岗岩的接触带,为单一萤石矿床。萤石矿石的稀土元素的含量(∑REE)变化范围为(8.04~30.04)×10-6,平均为19.42×10-6;轻重稀土LREE/HREE值0.24~0.65,平均0.52;LaN/YbN为0.07~0.62,平均0.26;δEu为0.42~0.90,平均0.60,具Eu负异常和明显重稀土富集的特征。岩矿石的Nd同位素研究表明,萤石矿石的εNd(t)都表现为很大的负值,以成矿主期年龄138Ma计算的εNd(138Ma)为-7.30~-30.55,具有古陆壳的演化特征,暗示其成矿的物质来源主要是壳源物质。在Moller的Tb/La-Tb/Ca成因判别图解中,敖包吐矿床的萤石的结晶作用表现为重新活化的趋势,反映流体具有混源的特征,既有热液成因,又有沉积成因。二叠世的海相火山活动通过海底喷气和喷流的作用形成了初始矿源层,而燕山中期花岗岩浆的侵位与结晶分异,又对初始矿源层的活化和富集提供了流体和热能的来源。成矿流体在经历了长期的演化后在大石寨组的构造薄弱破碎的的部位沉淀析出,形成敖包吐萤石矿床。  相似文献   
42.
江西德兴矿集区水系沉积物重金属污染的时空对比   总被引:5,自引:0,他引:5  
对比研究矿山开采一定时段内区域环境污染的时空变化特征,对于动态监测矿山开采对区域环境质量的影响情况、污染趋势等,具有重要的科学意义和实际价值。本文在利用2004年野外采集与测试分析的330个水系沉积物样品重金属含量数据基础上,充分利用矿山开采早期(1989)的1:20万乐平幅(As、Hg、Cd、Cr、Zn、Cu、Pb)水系沉积物地球化学图,通过数据预处理,分别对样品采集点重金属元素含量的统计分析和地质累积指数法评价的基础上,采用GIS的三维空间分析功能,对比研究德兴地区水系沉积物重金属污染时空变化。研究结果表明,十几年来,矿山开采对区域水系沉积物已造成了严重的污染,主要集中分布在是德兴铅锌和铜钼矿区德兴河与大坞河流域及其周边地区、乐安河下游沿岸局部地区、西北煤矿区以及乐安河下游乐平附近的煤矿区。  相似文献   
43.
通过研究太原盆地大气干湿沉降中重金属元素的含量分布特征及年输入通量,讨论其对土壤中重金属元素累积的影响。同时采用富集因子法探讨降尘物质的来源。研究结果表明,降尘中重金属元素As、Cd主要来源于人为活动,Pb的来源可能是人为源和自然源。而Hg则主要来源于自然源。  相似文献   
44.
滇西沘江流域水体中重金属元素的地球化学特征   总被引:6,自引:1,他引:5  
通过测定流经兰坪金顸铅锌矿区的沘江水体中Pb、Zn、Cd、As的含量和底泥中重金属元素的化学形态的含量,分析了重金属元素的分布和化学形态的变化。结果表明,沘江水遭到了Cd污染,底泥已经成为重金属元素的蓄积库,以国家土壤环境质量标准(Ⅲ级)衡量,Pb、Zn、Cd和舡分别超标3.4倍、15.8倍、106倍和2.6倍。沘江水中重金属元素含量的峰值在矿山附近的下游,而底泥中重金属元素的峰值在矿山下游30-50km的地方,矿业活动、水流变缓、pH等水体环境条件的变化都能影响水和底泥中重金属元素的含量。底泥中的Pb以碳酸盐结合态为主,Zn和Cd以铁锰氧化物结合态为主,而As以残渣态为主。Pb、Cd、Zn三种元素的环境有效态含量比较高,对沘江流域生态环境具有潜在的巨大的危害。  相似文献   
45.
In northern Jiangsu coastal zone area, Guanhe River is the biggest river and has the best navigation conditions among rivers which flow into the Yellow Sea. The grain sizes show gradual increase from the high intertidal zone to lower intertidal zone. The heavy metal values have slight changes along both sides of the river mouth, but show an evident change perpendicular to the tidal flat. In the latter case, they show a good correlation with grain size fluctuation, that is, the heavy metal values gradually decline when the grain size increases from the high intertidal zone to the lower intra-tidal zone. Analyses of the heavy metal elements show that on the Guanhe estuary surface sediment, the content of the elements Hg, As and Cu is above background values; Pb and Zn contents are rather close to the background values; and Cd content is less than the background values. The element Hg comes out to be harmful in a medium level to ecological environment, while the elements of Cr, As, Cu, Pb, Zn and Cd fall in a safe range of MPL. On the whole, Guanhe estuary tidal flat is not very harmful to the ecology in terms of the heavy metals. __________ Translated from Marine Geology & Quaternary Geology, 2007, 27(5): 23–32 [译自: 海洋地质与第四纪地质]  相似文献   
46.
47.
The hypermarine southern Coorong is threatened by proposals to drain relatively fresh surface water and groundwater from adjacent agricultural areas into the Coorong. These influent waters carry moderate loads of heavy metals. Acute toxicity of heavy metals toDiacypris compacta, an abundant ostracod in the Coorong, was measured in the laboratory at 18°C in a static system using Coorong water (pH 7.8 salinity 50 ppt). At 4 days (96 h) the mean values of LC50 for copper, zinc, lead and, cadmium respectively were 0.8, 2.1, 3.1 and 4.3 mg L–1, and at 8 days the respective mean LC50 s were 0.4, 0.7, 2.2 and 1.1 mgL–1. The effect of two or three metals on mortality was additive in some cases and synergistic in other cases, but generally less than additive. However, in all cases mortality was greater in the presence of two or three metals than in the presence of a single metal. According to ANZECC (1992) guidelines, maximum acceptable concentrations of heavy metals should be no higher than 0.01 x the lowest LC50 value. Using the lowest LC50 values forDiacypris compacta obtained at 8 days, maximum acceptable concentrations in the Coorong would be 4, 5, 9 and 22 gL–1 for copper, zinc, cadmium and lead respectively, the values for zinc and copper failling below those recommended by ANZECC (1992) for marine waters. Reported concentrations of copper and zinc in surface water and groundwater in areas adjacent to the Coorong sometimes exceed these values, hence drainage of these waters into the Coorong represents a significant hazard to the Coorong biota.  相似文献   
48.
The Taojiang Mn ore deposit was exploited in the early 1960s, and waste rocks were developed since then. Because the Mn ores were hosted within the metal-enriched black shales (Peng et al., 2004), the continuous mining has led to the exposure of an immense quality of black shales, which might cause serious impacts on environments. The present study deals with this environmental issue with samples from the waste rocks, and from the surrounding soils and surface water. The mineralogy of the waste rock was studied using EMPA, then a large number of elements in all waste rock, soil, and water samples were analyzed at a wide range of concentrations with high accuracy using an Elan6000 ICP-MS machine at Guangzhou Institute of Geochemistry, Chinese Academy of Sciences. The waste rock is composed mostly of black shales, with minor Mn carbonates. Both black shales and Mn carbonates of the waste rock contain many sulfide minerals, mainly pyrite, with minor galena, sphalerite, chalcopyrite, and others. The waste rocks are enriched in many metals including Sc, V, Cr, Co, Ni, Fe, Mn, Cu, Zn, Pb, Th, U, Mo, Sb, Sn, Tl, and others, and the metals are mostly hosted within the sulfides. Weathering of waste rocks might cause emission of the following metals: V, Cd, Ni, Th, U, Mo, Sb, Tl, Sc, Cr, Cu, Zn, Sn, and minor Co, and Pb. The surrounding soils are highly enriched in Cr, Co, Cu, Zn, Mn, Mo, Cd, Tl, and Pb, with the enrichment factors of 2.67.3.8, 7.26, 7.27, 8.2, 5.7, 13, and 5.4, respectively. The element ratios (Rb/Cs, Fe/Mn, Nb/Zr, Hf/Zr, and Ba/Sr) and REE distribution patterns of the soils are similar to those of the waste rocks and bedrocks.  相似文献   
49.
It has been found that stream waters were severely contaminated with wastes from a long-time smelting factory in Hezhang, Guizhou, China. The main sources of contamination are the smelting wastes stored in the open air and abandoned in the vicinity of stream. A method of lead isotope was adopted in order to identify relations between tailings and water contamination. Representative samples of tailings and stream sediments were collected. Mineralogical characterizations were conducted using XRD and TEM/SEM, while acid digestion was carried out for determining metal contents. BCR sequential leaching tests were performed in order to assess metal mobility. The tremendous ‘actual' and ‘potential' mobility of heavy metals indicates that the smelting waste and stream sediments present a considerable threat to the environment. Besides the chemical remobilization of heavy metals from the sediments and the reworking of riverbed sediments act as a secondary source of pollution. Also groundwater and stream water were sampled in specific locations and were measured.  相似文献   
50.
Since industrial revolution, the "greenhouse effect" is one of the most important global environmental issues. Of all the greenhouse gases, CO2 is responsible for about 64% of the enhanced "greenhouse effect", making it the target for mitigation, so reducing anthropogenic discharge of carbon dioxide attracts more and more attention. Geological sequestration of CO2 in deep saline aquifers is one of the most promising options. But because unknown fractures and faults may exist in the caprock layers which can prevent the leakage of CO2, CO2 will leak upward into upper potable aquifers, and lead to adverse impacts on the shallow potable aquifers. In order to assess the potential effect of CO2 leakage from underground storage reservoirs on fractures and water quality of potable aquifers, this study used the non-isothermal reactive geochemical transport code TOUGHREACT developed by Xu et al to establish a simplified 2-D model of CO2 underground sequestration system, which includes deep saline aquifers, caprock layers, and shallow potable aquifers, and study and analyze the changes of mineral and aqueous components. The simulation results indicated that the minerals of deep saline aquifers and fractures should be mainly composed of aluminosilicate and silicate minerals, which not only enhance the mass of CO2 sequestrated by mineral trapping, but also decrease the porosity and permeability of caprock layers and fractures to prevent and reduce CO2 leakage. The results from deep saline aquifers showed that the mass of carbon dioxide trapped by minerals and solution phases is limited, the rest remained as a supercritical phase, and so once the caprock aquifers have some unknown fractures, the free carbon dioxide phase may leak from CO2 geologic sequestration reservoirs by buoyancy.  相似文献   
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