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101.
Geochemical analysis of dump materials from the opencast Maritsa Iztok mines, Bulgaria, was carried out based on biomarker assemblages of hydrocarbon fractions. Organic matter (OM) and secondary transformations in three representative samples (massive black claystones and materials from the Iztok and Staroselets dump sites) were studied using geochemical proxies.A number of differences were recognised in the respective OM compositions of the samples compared to both published data and between the individual dump samples themselves. The ОM of the studied samples was found to be polar, but also contains some apolar compounds. It consists mainly of resins and asphalthenes. Claystone OM is of the dispersed type, with intense oxidative-reductive interactions in a lacustrine environment resulting in its transformation into an inert material. Dump sample kerogen is of Type II and mixed Type II/III. In all samples, “odd” numbered n-alkanes are found in higher amounts. Diterpenoids (С19, С20) with pimarane, abietane and phyllocladane skeletons are preponderant. Tri- and tetracyclic terpenoids and steranes have been identified in the black claystones OM only. Hopanes are present in low amounts in extractable OM from all three samples. Biomarkers indicate that black claystone OM is formed from aqueous flora, with a minor supply of gymnosperms (mainly G. Sequoia). Iztok Dump OM is structured by higher plants with an aqueous vegetation input. The Staroselets Dump OM formation is assigned to an active microbial reworking of aqueous vegetation and bacteria with a minor coniferous supply. Different geochemical parameters admit anoxic stratified bottom waters for the black claystones with an addition of deep water stagnation for Staroselets sample in a Maritsa Iztok Basin (MIB) aqueous environment.An attempt was also made to track the effect of secondary processes (oxidation, destruction, dearomatisation), temperature, water drainage and wash-out on dump materials. Leaching and weak degradation processes in the MIB dump environment are likely for a time span of ca. 40–50 years, considering the low percentage of short-chain n-alkanes, long-chain prevalence and low Pr/nC17 and Ph/nC18 ratios, with the Iztok Dump sample experiencing more advanced transformations.  相似文献   
102.
以矿田构造–岩相填图为主要方法,研究确定矿田构造和岩浆-热力构造类型及矿床类型,进行成矿富集中心的圈定及找矿预测,是矿田构造背景复杂地区的有效调研方法之一。东昆仑西段祁漫塔格矿带多期构造–岩浆活动强烈,断裂发育,以印支晚期岩浆侵入成矿与找矿进展较大。本次选择景忍–虎头崖、卡尔却卡B区、乌兰乌珠尔三个矿田区,进行1∶10000构造–岩相填图,填制了三个矿田区岩浆–热力构造类型分布图,认为晚三叠世岩浆侵入作用是该区多金属大规模成矿的主要内因,叠加其上的不同方向断裂控矿作用不同,近东西向和北西西向断裂控矿显著,明确了各矿田构造背景和印支期岩浆侵入形成的花岗斑岩+矽卡岩+断裂带热液成矿的模式,厘定了岩浆–热力构造的识别标志,即主要是印支晚期中酸性侵入岩、花岗斑岩、矽卡岩带、大理岩带、接触交代蚀变带、断裂破碎带叠加热液蚀变带等,圈定了成矿和找矿富集中心。  相似文献   
103.
湘西北寒武系沉积型镍钼矿成矿物质来源   总被引:1,自引:0,他引:1  
闫友谊 《江苏地质》2016,40(4):560-566
湘西北寒武系含矿丰富,在寒武系下统牛蹄塘组黑色岩系中赋存有磷矿、石煤、钒矿、铀矿,并有有色金属钼、镍矿及铂族元素矿物聚集。通过分析总结前人成果资料,探究镍钼矿成矿地质环境条件是在低温环境、有微生物参与及强还原环境中同生沉积,对寒武系沉积型镍钼矿成矿物质来源提出了明确的看法,即成矿物质来源于海底喷流-热水。  相似文献   
104.
位于扬子陆块西缘与西南三江造山带结合部位的乡城-丽江地区,北起四川乡城经云南格咱南至丽江地区,在印支期斑岩铜矿带上新发现叠加了燕山期斑岩Mo多金属成矿作用,形成乡城-丽江斑岩Mo矿带。受印支期古特提斯洋盆闭合后地壳缩短与加厚的影响,燕山晚期下地壳发生拆沉作用,导致后碰撞型花岗质岩浆侵位,发育了Mo多金属成矿作用,并构成斑岩成矿系统。岩石地球化学特征表明,燕山晚期含矿斑岩具高硅(SiO_2=66.29%~79.36%)、高碱(K_2O+Na_2O=5.07%~9.24%)、富钾(K_2O/Na_2O=0.71~2.13)的特点,属于高钾钙碱性岩石系列。岩石富集轻稀土元素(LREE),具有负δEu异常;微量元素具富集大离子亲石元素K、U、Th、Rb,亏损高场强元素Nb、Ta、P、Ti的特征;大离子亲石元素的富集和Nb、Ta等高场强元素的亏损,表明形成这些岩体的岩浆主要来自地壳,具有造山带花岗岩的地球化学特征。区内代表性含矿斑岩相似的地球化学组成及分布特征表明,乡城-丽江结合带燕山晚期的成矿斑岩是由同源岩浆分异演化而来。成矿系统的分析表明,燕山晚期主要含矿斑岩成矿物质以壳源为主,但具有少量地幔物质的加入,成岩成矿物质来源具有相似或一致的源区特征。在成矿元素的组合上,由成矿斑岩体向外带表现出W、Mo→W、Mo、Cu→Pb、Zn、Ag的演化趋势。研究表明,本区燕山晚期花岗岩浆的侵入及Mo多金属成矿作用并不是独立或个别的成矿事件,而是纵跨义敦岛弧、甘孜-理塘结合带及扬子西缘的带状成矿活动,属于区内与燕山晚期岩浆侵入作用相关的统一斑岩成矿系统。  相似文献   
105.
The double‐spike method with multi‐collector inductively coupled plasma‐mass spectrometry was used to measure the Mo mass fractions and isotopic compositions of a set of geological reference materials including the mineral molybdenite, seawater, coral, as well as igneous and sedimentary rocks. The long‐term reproducibility of the Mo isotopic measurements, based on two‐year analyses of NIST SRM 3134 reference solutions and seawater samples, was ≤ 0.07‰ (two standard deviations, 2s, n = 167) for δ98/95Mo. Accuracy was evaluated by analyses of Atlantic seawater, which yielded a mean δ98/95Mo of 2.03 ± 0.06‰ (2s, n = 30, relative to NIST SRM 3134 = 0‰) and mass fraction of 0.0104 ± 0.0006 μg g?1 (2s, n = 30), which is indistinguishable from seawater samples taken world‐wide and measured in other laboratories. The comprehensive data set presented in this study serves as a reference for quality assurance and interlaboratory comparison of high‐precision Mo mass fractions and isotopic compositions.  相似文献   
106.
The Lamont‐Doherty Earth Observatory radiogenic isotope group has been systematically measuring Sr‐Nd‐Pb‐Hf isotopes of USGS reference material BCR‐2 (Columbia River Basalt 2), as a chemical processing and instrumental quality control monitor for isotopic measurements. BCR‐2 is now a widely used geochemical inter‐laboratory reference material (RM), with its predecessor BCR‐1 no longer available. Recognising that precise and accurate data on RMs is important for ensuring analytical quality and for comparing data between different laboratories, we present a compilation of multiple digestions and analyses made on BCR‐2 during the first author's dissertation research. The best estimates of Sr, Nd and Hf isotope ratios and measurement reproducibilities, after filtering at the 2s level for outliers, were 87Sr/86Sr = 0.705000 ± 11 (2s, 16 ppm, n = 21, sixteen digestions, one outlier), 143Nd/144Nd = 0.512637 ± 13 (2s, 25 ppm, n = 27, thirteen digestions, one outlier) and 176Hf/177Hf = 0.282866 ± 11 (2s, 39 ppm, n = 25, thirteen digestions, no outliers). Mean Nd and Hf values were within error of those reported by Weis et al. (2006, 2007) in their studies of RMs; mean Sr values were just outside the 2s uncertainty range of both laboratories. Moreover, a survey of published Sr‐Nd‐Hf data shows that our results fall within the range of reported values, but with a smaller variability. Our Pb isotope results on acid leached BCR‐2 aliquots (n = 26, twelve digestions, two outliers) were 206Pb/204Pb = 18.8029 ± 10 (2s, 55 ppm), 207Pb/204Pb = 15.6239 ± 8 (2s, 52 ppm), 208Pb/204Pb = 38.8287 ± 25 (2s, 63 ppm). We confirm that unleached BCR‐2 powder is contaminated with Pb, and that sufficient leaching prior to digestion is required to achieve accurate values for the uncontaminated Pb isotopic compositions.  相似文献   
107.
新疆萨尔朔克金铜多金属矿床产于中泥盆统阿舍勒组上亚组的中酸性火山岩-次火山岩中,地表以金(铜)矿化为主,矿体形态及空间分布严格受NNW向断裂破碎带控制,矿体呈脉状、透镜状。金(铜)矿石以蚀变岩型为主,其次为石英脉型,赋矿围岩为黄铁绢英岩化流纹斑岩。金主要赋存在微细粒黄铁矿等硫化物和脉石英中,黄铜矿常呈不规则细脉状出现。在地表100m以下,出现铅锌矿化,且向深部铅锌品位较高,一般3%~5%,最高达12%以上。流纹斑岩与金铜多金属矿关系密切。通过锆石U-Pb同位素测年和Hf同位素测试分析,获得流纹斑岩的成岩年龄为386.2±1.5Ma,εHf(t)在7~13之间,主要集中在8.5~12.5之间。上述结果表明,流纹斑岩可能形成于早泥盆世晚期活动大陆边缘环境,是俯冲增生的产物。铅锌矿化是386Ma流纹斑岩期后岩浆作用的产物,而金铜矿化则是在含矿流纹斑岩的基础上,经其后火山热液叠加作用发生的。  相似文献   
108.
Trace elements from samples of bauxite deposits can provide useful information relevant to the exploration of the ore‐forming process. Sample digestion is a fundamental and critical stage in the process of geochemical analysis, which enables the acquisition of accurate trace element data by ICP‐MS. However, the conventional bomb digestion method with HF/HNO3 results in a significant loss of rare earth elements (REEs) due to the formation of insoluble AlF3 precipitates during the digestion of bauxite samples. In this study, the digestion capability of the following methods was investigated: (a) ‘Mg‐addition’ bomb digestion, (b) NH4HF2 open vessel digestion and (c) NH4F open vessel digestion. ‘Mg‐addition’ bomb digestion can effectively suppress the formation of AlF3 and simultaneously ensure the complete decomposition of resistant minerals in bauxite samples. The addition of MgO to the bauxite samples resulted in (Mg + Ca)/Al ratios ≥ 1. However, adding a large amount of MgO leads to significant blank contamination for some transition elements (V, Cr, Ni and Zn). The NH4HF2 or NH4F open vessel digestion methods can also completely digest resistant minerals in bauxite samples in a short period of time (5 hr). Unlike conventional bomb digestion with HF/HNO3, the white precipitates and the semi‐transparent gels present in the NH4HF2 and NH4F digestion methods could be efficiently dissolved by evaporation with HClO4. Based on these three optimised digestion methods, thirty‐seven trace elements including REEs in ten bauxite reference materials (RMs) were determined by ICP‐MS. The data obtained showed excellent inter‐method reproducibility (agreement within 5% for REEs). The relative standard deviation (% RSD) for most elements was < 6%. The concentrations of trace elements in the ten bauxite RMs showed agreement with the limited certified (Li, V, Cr, Cu, Zn, Ga, Sr, Zr and Pb) and information values (Co, Ba, Ce and Hf) available. New trace element data for the ten RMs are provided, some of which for the first time.  相似文献   
109.
Due to intensive research into selenium isotopes in recent years, the increasing requirement for reliable and comparable measurement results has created a strong demand for selenium isotopic certified reference materials (iCRM) that were previously not available. To address this, eleven selenium iCRMs were developed, including ten synthetic iCRMs (GBW 04447–GBW 04456) and one natural iCRM (GBW 04457). The synthetic iCRMs were prepared with 76Se, 78Se, 80Se and 82Se solutions and a natural selenium solution; the natural iCRM was prepared with highly pure selenium material. The property values of isotope ratios in these iCRMs were certified by calibrated mass spectrometry with a collision cell multi‐collector ICP‐MS. The mass discrimination effect of the instrument was corrected with corresponding 78Se/76Se isotope mixtures and 82Se/76Se isotope mixtures, which were gravimetrically prepared with purified, isotopically enriched selenium materials. Homogeneity and stability tests were performed, and no significant influences were found. The uncertainty of the property values of the iCRMs was evaluated according to the Guide to the Expression of Uncertainty in Measurement (GUM) of ISO/BIPM and ISO Guide 35. The δ82/76Se value of GBW 04457 relative to NIST SRM 3149 was also calculated. These iCRMs are intended for use in calibration of instruments and evaluation of methods for the determination of selenium isotope ratios.  相似文献   
110.
张家口市崇礼区北部完成了1∶5万地球化学测量,小西湾侵入岩位置恰与化探工作圈定的AS33,即小西湾综合异常高度套合。利用区域资料及异常查证所获得的大比例尺地质、物化探数据,对该区成矿条件进行了综合分析,并推测了矿化蚀变的形成机制及其矿化蚀变体主要赋存位置。通过推断该区矿化机制并建立模型,认为该区具有寻找中高温热液型多金属矿床的潜力,并对下一步的勘查方向提出了建议。  相似文献   
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