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81.
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   
82.
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   
83.
An array of large concentric porous cylinder arrays is mounted in shallow water exposed to cnoidal waves. The interactions between waves and cylinders are studied theoretically using an eigenfunction expansion approach. Semi-analytical solutions of hydrodynamic loads and wave run-up on each cylinder are obtained using first approximation to cnoidal waves. The square array configuration of four-legged identical concentric porous cylinder is investigated in present study. Numerical results reveal the variation of dimensionless wave force and wave run-up on individual cylinder with angle of incidence, porosity parameter, spacing between outer and inner cylinders, spacing between concentric porous cylinders and wave parameter. Different mechanism of wave force is found under different range of scattering parameter.  相似文献   
84.
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   
85.
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   
86.
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   
87.
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   
88.
冻融循环对不同孔隙率页岩相似材料影响的试验研究   总被引:2,自引:2,他引:0  
基于地质力学模型试验的相似理论,针对寒区岩体工程,分别制作了5种不同孔隙率的页岩相似材料,进行冻融循环试验,探究不同孔隙率的页岩相似材料在冻融前后,其主要物理力学参数的变化规律。试验研究表明:在冻融循环后,页岩相似材料的单轴抗压强度、三轴抗压强度、弹性模量、粘聚力、内摩擦角有不同程度的减小,孔隙率、泊松比有不同程度的增大。页岩相似材料的物理力学参数受冻融循环的影响随孔隙率的增大先增大后减小,孔隙率处于9.4%~13.6%时,受冻融循环影响最大;孔隙率处于5.8%~9.4%时,受冻融循环的影响随孔隙率的增大有增大的趋势;孔隙率处于13.9%~19.1%时,受冻融循环的影响随孔隙率的增大有减小的趋势。研究结果可以为西部寒区的岩土工程建设和减灾提供相关的科学依据。  相似文献   
89.
谢小敏  刘伟新  张瀛  赵迪斐  唐友军  申宝剑  李志明 《地质论评》2021,67(1):67020014-67020014
四川盆地下古生界两套硅质页岩层系是其重要的页岩气产层,五峰组—龙马溪组硅质含量与TOC及含气量呈正相关性,暗示硅质矿物对该地区页岩气的生成具有重要意义。但硅质来源复杂,且存在后期硅质流体的注入。因此,本文在总结前人的研究成果基础上,对四川盆地寒武系底部硅质岩系与五峰组—龙马溪组硅质岩系的硅质特征进行了详细的岩石学分析,揭示了3种硅质来源特征:①同沉积无机硅质流体;②生物硅;③后期无机硅质流体。其中寒武系底部以同沉积无机硅质流体与生物硅来源为主,同沉积硅质流体导致有机质快速石化埋藏,有机质内部结构及形态保存较好;五峰组—龙马溪组硅质来源以后期无机硅质流体与生物硅来源为主,有机质在保存过程中受硅质流体的影响很小,有机质腐泥化作用充分,内部结构和形态多数保存较差。该研究初步揭示了两套页岩层系的硅质发育岩石学特征,及其对有机质保存的影响,期望能为四川盆地两套页岩气储层差异性提供新的思路与基础地质数据。  相似文献   
90.
通常样品的87Sr/86Sr和143Nd/144Nd同位素比值分析采用SRM987、JNdi-1作为标准物质,它们分别是纯的碳酸盐和氧化物,适用于监控质谱测试过程。中国现有的钐-钕地质和铷-锶年龄标准物质,分别为玄武岩和钾长石,它们与很多地质样品的基质存在差别。仅有这两种基质的标准物质不能有效地监控不同地质样品Rb-Sr、Sm-Nd同位素分析过程,因此研制不同岩性的Rb-Sr、Sm-Nd同位素标准物质具有重要现实意义。本文采集中国典型地区的橄榄岩、榴辉岩和花岗岩作为候选物,严格按照《一级标准物质技术规范》(JJF 1006-1994)和《标准物质定值的通用原则及统计学原理》(JJF 1343-2012)等相关标准物质国家计量技术规范和国家标准,研制了橄榄岩、榴辉岩和花岗岩铷-锶、钐-钕同位素标准物质(编号为GBW04139、GBW04140、GBW04141),其中橄榄岩标准物质适用于高Mg、Fe,低Rb、Nd含量样品的分析,榴辉岩和花岗岩标准物质适用于含有难溶副矿物的岩石样品的分析。每个标准物质具有6个特性量值,Rb、Sr、Sm和Nd含量分布分别为0.16~64μg/g、12~560μg/g、0.1~3.2μg/g和0.3~15.3μg/g,87Sr/86Sr比值分布为0.70446~0.71309,143Nd/144Nd比值分布为0.51115~0.51267,同位素比值精度达到或优于同类标准物质。这些特性量值更接近实际样品,使用时将更加有效和方便。该系列标准物质可用于校准仪器和评价方法,并能有效监控实验室此类样品的铷-锶、钐-钕同位素分析过程。  相似文献   
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