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61.
The mimetic ocean environment and chemical method were used to research the bioavailability effect of humic acid on five heavy metals in sediment, including Cd, Cu, Zn, Pb and Ni. The sediment was separated into four containers with artificial seawater, and each of them had different concentrations of humic acid. The values of concentrations covered the whole range found in natural sediment (0.1%-10%). According to the 48 hours LC50 of clam and distribution coefficient, metals were added in artificial seawater, and their speciation was determined at first and then after two days' incubation. It was found the bioavailability of heavy metals was reduced in the presence of humic acid. The obvious negative effect on Zn was observed, but the influence on Cd was not remarkable. In addition, the contents of Pb and Ni increased obviously in organic phase, and they are correlative with the concentrations of humic acid.  相似文献   
62.
As the diversion dike of the Middle Route of the South to North Water Transfer Project (MRSNWTP), the water quality and water quantity of Danjiangkou Reservoir is critical to the project. At present, the rates of industrial wastewater treatment and sewage discharge, which belongs to Chinese State Standard in the districts near the reservoir except Shiyan city, are less than 60% and 40% respectively. The point source pollutants will be controlled because of the project after some time, but the non-point source pollutants caused by vegetation degradation and water-soil erosion will not be controlled effectively in a long time. Water samples were collected from the Danjiangkou Reservoir during 2004 and 2005 and analyzed for trace metals, i.e., silver (Ag), aluminum (Al), arsenic (As), barium (Ba), bismuth (Bi), calcium (Ca), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), mercury (Hg), potassium (K), lithium (Li), magnesium (Mg), manganese (Mn), molybdenum (Mo), sodium (Na), nickel (Ni), lead (Pb), antimony (Sb), selenium (Se), silicon (Si), strontium (Sr), vanadium (V), zinc (Zn), chemicophysical parameters and nutrients, i.e., temperature (T), pH, dissolved oxygen (DO), turbidity, total suspended solid (TSS), nitrate/ammonia/ammonium-nitrogen (NO3^-/NH3/NH4^+-N), total nitrogen (TN), dissolved inorganic nitrogen (DIN), total phosphorus (TP), potassium permanganate index (IMn), biochemical oxygen demand (BOD), dissolved inorganic carbon (HCO3^-). Our results are water quality belongs to Chinese standard level II, trace metals are low, but they are accumulating, and many of which, i.e., As, Pb, will endanger reservoir water security.  相似文献   
63.
采集和分析了五通桥区不同功能区和乡镇73个土壤样品,以了解山丘平原过渡区土壤重金属的含量和污染特征。结果表明,重金属的平均含量为Pb32.18mg/kg、Cd0.82mg/kg、Cu28.61mg/kg、Zn108.08mg/kg、Ni32.66mg/kg、Cr72.44mg/kg;与四川土壤背景值相比,Cu、Ni、Cr的含量与之持平,Pb增加了0.11倍,Zn增加了0.32倍,Cd的积累较为严重,比背景值增加了10倍。污染评价结果显示该过渡区存在一定程度的重金属污染问题,不同功能区的污染程度排序为工业区〉生活区〉农业区。Cd在六种元素的土壤污染分担率中占55.46%,是最主要的污染元素;土壤Cd含量与Pb和Zn存在较高的相关性(相关系数为0.525和0.500),表明存在Pb—Cd和Zn—Cd的复合污染。  相似文献   
64.
Platinum-group element (PGE) mineralisation within the Platreef at Overysel is controlled by the presence of base metal sulphides (BMS). The floor rocks at Overysel are Archean basement gneisses, and unlike other localities along the strike of the Platreef where the floor is comprised of Transvaal Supergroup sediments, the intimate PGE–BMS relationship holds strong into the footwall rocks. Decoupling of PGE from BMS is rare and the BMS and platinum-group mineral assemblages in the Platreef and the footwall are almost identical. There is minimal overprinting by hydrothermal fluids; therefore, the mineralisation style present at Overysel may represent the most ‘primary’ style of Platreef mineralisation preserved anywhere along the strike. Chondrite-normalised PGE profiles reveal a progressive fractionation of the PGE with depth into the footwall, with Ir, Ru and Rh dramatically depleted with depth compared to Pt, Pd and Au. This feature is not observed at Sandsloot and Zwartfontein, to the south of Overysel, where the footwall rocks are carbonates. There is evidence from rare earth element abundances and the amount of interstitial quartz towards the base of the Platreef pyroxenites that contamination by a felsic melt derived from partial melting of the gneissic footwall has taken place. Textural evidence in the gneisses suggests that a sulphide liquid percolated down into the footwall through a permeable, inter-granular network that was produced by partial melting around grain boundaries in the gneisses that was induced by the intrusion of the Platreef magma. PGE were originally concentrated within a sulphide liquid in the Platreef magma, and the crystallisation of monosulphide solid solution from the sulphide liquid removed the majority of the IPGE and Rh from it whilst still within the mafic Platreef. Transport of PGE into the gneisses, via downward migration of the residual sulphide liquid, fractionated out the remaining IPGE and Rh in the upper parts of the gneisses leaving a ‘slick’ of disseminated sulphides in the gneiss, with the residual liquid becoming progressively more depleted in these elements relative to Pt, Pd and Au. Highly sulphide-rich zones with massive sulphides formed where ponding of the sulphide liquid occurred due to permeability contrasts in the footwall. This study highlights the fact that there is a fundamental floor rock control on the mechanism of distribution of PGE from the Platreef into the footwall rocks. Where the floor rocks are sediments, fluid activity related to metamorphism, assimilation and later serpentinisation has decoupled PGE from BMS in places, and transport of PGE into the footwall is via hydrothermal fluids. In contrast, where the floor is comprised of anhydrous gneiss, such as at Overysel, there is limited fluid activity and PGE behaviour is controlled by the behaviour of sulphide liquids, producing an intimate PGE–BMS association. Xenoliths and irregular bands of chromitite within the Platreef are described in detail for the first time. These are rich in the IPGE and Rh, and evidence from laurite inclusions indicates they must have crystallised from a PGE-saturated magma. The disturbed and xenolithic nature of the chromitites would suggest they are rip-up clasts, either disturbed by later pulses of Platreef magma in a multi-phase emplacement or transported into the Platreef from a pre-existing source in a deeper staging chamber or conduit.  相似文献   
65.
This study examines the removal of dissolved metals during the oxidation and neutralization of five acid mine drainage (AMD) waters from La Zarza, Lomero, Esperanza, Corta Atalaya and Poderosa mines (Iberian Pyrite Belt, Huelva, Spain). These waters were selected to cover the spectrum of pH (2.2–3.5) and chemical composition (e.g., 319–2,103 mg/L Fe; 2.85–33.3 g/L SO4=) of the IPB mine waters. The experiments were conducted in the laboratory to simulate the geochemical evolution previously recognized in the field. This evolution includes two stages: (1) oxidation of dissolved Fe(II) followed by hydrolysis and precipitation of Fe(III), and (2) progressive pH increase during mixing with fresh waters. Fe(III) precipitates at pH < 3.5 (stages 1 and 2) in the form of schwertmannite, whereas Al precipitates during stage 2 at pH 5.0 in the form of several hydroxysulphates of variable composition (hydrobasaluminite, basaluminite, aluminite). During these stages, trace elements are totally or partially sorbed and/or coprecipitated at different rates depending basically on pH, as well as on the activity of the SO4= anion (which determines the speciation of metals). The general trend for the metals which are chiefly present as aqueous free cations (Pb2+, Zn2+, Cu2+, Cd2+, Mn2+, Co2+, Ni2+) is a progressive sorption at increasing pH. On the other hand, As and V (mainly present as anionic species) are completely scavenged during the oxidation stage at pH < 3.5. In waters with high activities (> 10−1) of the SO 4= ion, some elements like Al, Zn, Cd, Pb and U can also form anionic bisulphate complexes and be significantly sorbed at pH < 5. The removal rates at pH 7.0 range from around 100% for As, V, Cu and U, and 60–80% for Pb, to less than 20% for Zn, Co, Ni and Mn. These processes of metal removal represent a significant mechanism of natural attenuation in the IPB.  相似文献   
66.
高敏感度、高可靠度、低花费传感器是全自动或半自动探雷机器人的首要和绝对的选择。当前,有许多技术能够被选来综合使用以满足上述的要求。金属探测器是一种传统的、成熟可靠的探测技术。但是,现在多种地雷含有少量的金属或者不包含任何金属,造成了用金属探测器探雷的困难。目前迫切需要研究发展新颖的探测技术以消除100万颗地雷对许多国家的影响。  相似文献   
67.
新疆绿色电气石颜色成因研究   总被引:5,自引:0,他引:5       下载免费PDF全文
新疆绿色电气石颜色成因比较特殊,为了更好地了解其颜色的形成,主要采用化学分析、吸收光谱、穆斯堡尔谱等测试手段对绿色电气石颜色成因进行研究。化学分析结果显示每个样品中均含有少量不同过渡元素离子,如Fe2 、Ti4 、Cr3 等,影响着绿色的形成;利用吸收光谱测试方法确定了致色离子的吸收带位置及主要离子的种类、价态,并根据化学成分计算出相应的化学式,利用穆斯堡尔谱确定了铁离子在晶体中的占位。综合运用上述测试方法,确定了绿色电气石的颜色成因。  相似文献   
68.
东天山晚古生代内生金属矿床成矿系列和成矿规律   总被引:12,自引:8,他引:12  
东天山造山带是我国重要的金铜矿产富集区之一,通过初步研究,按照成矿系列的学术思想将区内金属矿床划分为6个矿床成矿亚系列,并对每个成矿亚系列形成的构造环境和主要地质作用进行了简要论述,进而探讨了该地区区域成矿规律与构造演化的关系,总结了该地区构造活动的时-空演化导致该地区独具特色的内生金属矿床侧向分带现象。  相似文献   
69.
阿尔金地区构造应力场及其对金属矿产分布的控制作用   总被引:2,自引:0,他引:2  
构造应力场研究可以为区域矿产预测提供依据。主要根据节理、擦痕的测试分析,结合区域构造解析,确定阿尔金山东西向拉配泉--红柳沟构造带经历了三期不同方向的应力作用:印支期以前的南北向挤压作用,印支-燕山期的北西-南东向的挤压和中生代晚期-新生代北东东-南南西向的挤压;并利用有限元数值模拟前两期构造应力场的演变过程,进而讨论了区域构造应力场对内生金属矿产分布规律的控制作用指出了区域寻找大型内生金属矿产的有利地段。  相似文献   
70.
This paper assesses the agricultural land resources of Guiyang City by means of GIS,on the basis of the pressure-state-response model in which soil heavy metal contamination is selected as a pressure indicatror.he results suggest that most of the agricultural land resources are of good quality,However,there are 17.11km^2 dry land and paddy field,which belong to the region of serious heavy metal contamination and are not fit for planting crops.At the same time,the high quality plowland,which is suitable for cultivation,has decreased nearly by 1/3 due to soil heavy metal contamination.These findings may improve our understanding that it is very important to prevent and cure heavy metal contamination of Guiyang City.  相似文献   
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