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Yong Zhang Shu–Wen Xing Chao Li Shi–Fu Liang Zheng–Tao Yu Xiao–Hui Du 《International Geology Review》2017,59(2):185-203
The Changfagou Cu deposit is a newly discovered porphyry deposit located in the southern Jilin Province of Northeastern China, on the northeastern margin of the North China Craton. To better understand the formation of the Cu deposit, we report the zircon U–Pb and molybdenite Re–Os dating, and Sr-, Nd-, and Hf- isotopic data of the granite porphyry. LA-ICP-MS dating of zircon grains from two mineral zones in the granite porphyry yield ages of 115.7 ± 0.8 and 115.3 ± 0.6 Ma, which is interpreted as the emplacement age of the granite porphyry. The molybdenite Re–Os model ages of 112.5 to 113.8 Ma, an isochron age of 113.3 ± 1.3 Ma, and a weighted mean model age of 113.0 ± 0.7 Ma, which represents the age of the Cu mineralization quite well. The Changfagou granite porphyry samples lack amphibole and muscovite, and are compositionally characterized by high SiO2, high Na2O+K2O, and low P2O5, enriched in some Rb, Th, U, and Pb, and depleted in Nb, Ta, Ti, P, and Eu. Mineralogical and geochemical features suggest that the Changfagou granite porphyry samples are slightly peraluminous and are of highly fractionated I-type granitoids. The granitic rocks also have relatively high (87Sr/86Sr)i (0.71199 to 0. 71422), and both low εNd(t) (?14.56 to ?13.19) and εHf(t) values (?14.916 to ?8.644), which suggest that Changfagou granite porphyry are derived from mixed sources of crustal and mantle, and diagenesis and mineralization were possibly related to the switch in subduction direction of the Palaeo-Pacific Plate in the late phase of Early Cretaceous. 相似文献
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996.
Most research on long chain methyl ketones has focused on their origins and distributions. Their application in paleoclimate studies is less common than that of other n-alkyl lipids. The goal of this research was to explore this potential by studying n-alkan-2-ones from the Hani peat sequence in northeastern China. They were identified using gas chromatography-mass spectrometry (GC-MS) and showed a distribution ranging from C19 to C31 with a strong odd/even predominance. This type of distribution is considered to derive from Sphagum and microbial oxidation of n-alkanes. Comparison with climate sensitive indicators and macrofossil analysis shows that microbial oxidation of n-alkanes derived from higher plants was enhanced during the warm early Holocene period. This led us to develop three n-alkan-2-one proxies - C27/ΣC23-31 (C27/HMW-KET), carbon preference index (CPIH-KET) and average chain length (ACL(27-31)-KET) - as possible indicators of paleoclimate in the peat-forming environment. These proxies, in combination with C27n-alkane δD values and peat cellulose δ18O records, might allow examination of paleo-ecosystem behavior during climatic evolution in northeastern China over the past 16,000 yr. 相似文献
997.
Geochemistry and origin of elements in some UK coals 总被引:3,自引:0,他引:3
Twenty-four UK coals ranging in rank with 4.6%–37.6% volatile matter were analysed for 46 major and trace elements. The samples were obtained from the UK Coal Bank and are representative of the major UK coal fields. The major element distributions are interpreted in terms of the mineralogical variations—quartz and kaolinite are largely responsible for the Si and Al, carbonates for Ca and Mg and pyrite for Fe. Also exerting an influence in some samples are siderite, Al-phosphate minerals and illite. Based on statistical relationships with the major elements, Rb, Cr, Th, Ce, Zr, Y, Ga, La, Ta, Nb and V are thought to be mainly present in the clay minerals, and As, Mo, Sb, Tl, Se and Bi and Pb are probably present in pyrite. Strontium and Ba are concentrated in a restricted number of samples related to the phosphate minerals. Germanium is the only element for which a major organic association can be demonstrated. Elements with an indirect association with the organic matter are Na, Cl, and Br in porefluids and possibly Te. The ash content is controlled mainly by the detrital input and the trace elements related to the ash content are therefore those elements associated with the clay minerals. Variations with rank would appear to be mainly related to the moisture content (porefluids). The trace elements associated with the quartz and clay minerals are thought to be dominantly detrital in origin. The non-detrital elements, essentially those contained in pyrite, are thought to have been incorporated in the depositional environment from waters with enhanced salinities through seawater ingress, hence there are positive relationships between S and trace element concentrations. 相似文献
998.
An Investigation of Digestion Methods for Trace Elements in Bauxite and Their Determination in Ten Bauxite Reference Materials Using Inductively Coupled Plasma‐Mass Spectrometry 下载免费PDF全文
Wen Zhang Liang Qi Zhaochu Hu Cunjiang Zheng Yongsheng Liu Haihong Chen Shan Gao Shenghong Hu 《Geostandards and Geoanalytical Research》2016,40(2):195-216
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
999.
大兴安岭中段塔尔气地区早白垩世花岗岩成因及形成构造环境 总被引:2,自引:0,他引:2
通过大兴安岭中段塔尔气地区三道桥和桑多尔岩体全岩地球化学、年代学和锆石Lu-Hf同位素资料,探讨了其形成时代、岩石成因、源区性质等方面问题。三道桥和桑多尔岩体分别由正长花岗岩和二长花岗岩组成。LA-ICP-MS锆石U-Pb定年结果表明三道桥和桑多尔岩体均形成于早白垩世,其年龄分别为143 Ma和141 Ma。岩石地球化学分析结果显示,三道桥和桑多尔岩体均为高钾钙碱性的I型花岗岩,具有相似的岩浆源区。上述两岩体的锆石ε_(Hf)(t)值为正值(分别为4.9~9.3和2.1~8.1),具较年轻的二阶段Hf模式年龄(t_(DM2)=598~882 Ma,676~1 062 Ma),暗示其源于新元古代—显生宙期间新增生地壳物质的部分熔融。结合区域研究资料,认为三道桥和桑多尔岩体的形成与蒙古-鄂霍茨克洋闭合后的岩石圈伸展密切相关。 相似文献
1000.
近年来,区域性的Nd-Hf同位素填图正成为探索岩石圈结构和演化,制约陆块边界位置和壳-幔相互作用以及它们与金属成矿作用耦合关系的重要研究方法。目前的研究主要集中于中国的拉萨地体以及澳大利亚太古宙尤冈克拉通,包括地体地壳性质与空间变化规律、成矿系统约束和区域找矿潜力等方面。本文以三江特提斯造山带为例,使用克里格插值法在MAPGIS平台完成同位素等值线图,基此解析三江地区岩石圈结构以及大规模成矿作用。Nd-Hf同位素填图支持昌宁-孟连缝合带为冈瓦纳和泛华夏古陆的分界。昌宁-孟连缝合带划分了两个εNd(t)同位素明显不同的异常区,缝合带以西表现为古老地壳基地组成,而缝合带以东部表现为较年轻的地体。三江特提斯造山带中不同类型与岩浆岩有关的发矿床大多汇聚在同位素边界处,这些同位素边界可能代表着地体边界或缝合带、岩浆弧。沿金沙江-哀牢山缝合带分布的斑岩型或斑岩-矽卡岩型Cu-(Mo)矿床,具有高εHf(t)正值和较高εNd(t)负值的特征,对应始新世钾质斑岩及有关的矿化。在腾冲-保山地块、义敦岛弧和临沧次地块,具有低εHf(t),低εNd(t)值岩浆岩分布特征,主要形成与过铝质花岗岩型有关的锡-钨矿床。因此,我们认为区域尺度的同位素填图对研究岩石圈结构和演化、解剖壳-幔相互作用机理、解析深部动力学机制和成矿机制、总结区域成矿规律和指导区域成矿潜力具有重要意义。 相似文献