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141.
142.
Gang Yu Jiangfeng Chen Chunji Xue Yuchuan Chen Fukun Chen Xiaoyue Du 《Ore Geology Reviews》2009,35(3-4):367-382
The Qingchengzi orefield in northeastern China, is a concentration of several Pb–Zn, Ag, and Au ore deposits. A combination of geochronological and Pb, Sr isotopic investigations was conducted. Zircon SHRIMP U–Pb ages of 225.3 ± 1.8 Ma and 184.5 ± 1.6 Ma were obtained for the Xinling and Yaojiagou granites, respectively. By step-dissolution Rb–Sr dating, ages of 221 ± 12 Ma and 138.7 ± 4.1 Ma were obtained for the sphalerite of the Zhenzigou Zn–Pb deposit and pyrargyrite of the Ag ore in the Gaojiabaozi Ag deposit, respectively. Pb isotopic ratios of the Ag ore at Gaojiabaozi (206Pb/204Pb = 18.38 to 18.53) are higher than those of the Pb–Zn ores (206Pb/204Pb = 17.66 to 17.96; Chen et al. [Chen, J.F., Yu, G., Xue, C.J., Qian, H., He, J.F., Xing, Z., Zhang, X., 2005. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone, northeastern China. Science in China Series D 48, 467–476.]). Triassic granites show low Pb isotopic ratios (206Pb/204Pb = 17.12 to 17.41, 207Pb/204Pb = 15.47 to 15.54, 208Pb/204Pb = 37.51 to 37.89) and metamorphic rocks of the Liaohe Group have high ratios (206Pb/204Pb = 18.20 to 24.28 and 18.32 to 20.06, 207Pb/204Pb = 15.69 to 16.44 and 15.66 to 15.98, 208Pb/204Pb = 37.29 to 38.61 and 38.69 to 40.00 for the marble of the Dashiqiao Formation and schist of the Gaixian Formation, respectively).Magmatic activities at Qingchengzi and in adjacent regions took place in three stages, and each contained several magmatic pulses: ca. 220 to 225 Ma and 211 to 216 Ma in the Triassic; 179 to 185 Ma, 163 to 168 Ma, 155 Ma and 149 Ma in the Jurassic, as well as ca. 140 to 130 Ma in the Early Cretaceous. The Triassic magmatism was part of the Triassic magmatic belt along the northern margin of the North China Craton produced in a post-collisional extensional setting, and granites in it formed by crustal melting induced by mantle magma. The Jurassic and Early Cretaceous magmatism was related to the lithospheric delamination in eastern China. The Triassic is the most important metallogenic stage at Qingchengzi. The Pb–Zn deposits, the Pb–Zn–Ag ore at Gaojiabaozi, and the gold deposits were all formed in this stage. They are temporally and spatially associated with the Triassic magmatic activity. Mineralization is very weak in the Jurassic. Ag ore at Gaojiabaozi was formed in the Early Cretaceous, which is suggested by the young Rb–Sr isochron age, field relations, and significantly different Pb isotopic ratios between the Pb–Zn–Ag and Ag ores. Pb isotopic compositions of the Pb–Zn ores suggest binary mixing for the source of the deposits. The magmatic end-member is the Triassic granites and the other metamorphic rocks of the Liaohe Group. Slightly different proportions of the two end-members, or an involvement of materials from hidden Cretaceous granites with slightly different Pb isotopic ratios, is postulated to interpret the difference of Pb isotopic compositions between the Pb–Zn–(Ag) and Ag ores. Sr isotopic ratios support this conclusion. At the western part of the Qingchengzi orefield, hydrothermal fluid driven by the heat provided by the now exposed Triassic granites deposited ore-forming materials in the low and middle horizons of the marbles of the Dashiqiao Formation near the intrusions to form mesothermal Zn–Pb deposits. In the eastern part, hydrothermal fluids associated with deep, hidden Triassic intrusions moved upward along a regional fault over a long distance and then deposited the ore-forming materials to form epithermal Au and Pb–Zn–Ag ores. Young magmatic activities are all represented by dykes across the entire orefield, suggesting that the corresponding main intrusion bodies are situated in the deep part of the crust. Among these, only intrusions with age of ca. 140 Ma might have released sufficient amounts of fluid to be responsible for the formation of the Ag ore at Gaojiabaozi.Our age results support previous conclusions that sphalerite can provide a reliable Rb–Sr age as long as the fluid inclusion phase is effectively separated from the “sulfide” phase. Our work suggests that the separation can be achieved by a step-resolution technique. Moreover, we suggest that pyrargyrite is a promising mineral for Rb–Sr isochron dating. 相似文献
143.
岩溶水锶元素水文地球化学特征 总被引:12,自引:9,他引:12
通过对桂林地区地下河系统不同类型岩溶水水样Sr2+含量和87Sr/86Sr值分析,得到如下结论:(1)桂林地区岩溶水中Sr2+含量普遍较低,流经不同岩层的地下水Sr2+含量不同,岩溶水中Sr2+含量随着Ca2+含量的增大而增大,随着Mg2+含量的增大而减小;地下河水中的Sr2+含量始终介于表层岩溶带水、饱水带裂隙水、地表坡面流和外源水(如果存在外源水补给)的最大、最小值之间.(2)流经不同岩层地下水的87Sr/86Sr值不同,流经砂岩层地下水87Sr/86Sr值较高,其次为流经白云岩层和灰岩层的地下水;地下河水87Sr/86Sr值也是介于表层岩溶带水、饱水带裂隙水、地表坡面流和外源水(如果有外源水补给)的最大、最小值之间.因此Sr2+和87Sr/86Sr能反映岩溶水形成的信息,是较理想的天然示踪剂,在岩溶水研究中具有很广阔的应用前景. 相似文献
144.
西藏努日Cu-W-Mo矿床是目前冈底斯成矿带上发现的唯一具有Cu-W-Mo矿化组合的大型矿床。然而,自该矿床上世纪发现以来,关于其成因类型,一直存在较大的争议。本次研究根据矿床地质特征对矿床成矿阶段进行了精确的划分,并以氧化物阶段和石英–硫化物阶段的白钨矿(Sch–A和Sch–B)为研究对象,通过LA-ICP-MS微量元素和Sr同位素测试分析,对矿床成矿流体来源、演化过程及成因进行深入探讨。扫描电镜–阴极发光(SEM-CL)图像显示,白钨矿Sch–A具有两个世代,暗色均质Sch–A1被浅色均质Sch–A2不规则交代;而白钨矿Sch–B具有“核–边”结构,核部Sch–B1呈深灰色、具有均匀生长环带,边部为浅灰色、均质的Sch–B2。白钨矿Sch–A的稀土元素球粒陨石标准化分布特征和Sr同位素数据指示,成矿流体早期来源于花岗闪长斑岩,后期因强烈的水–岩反应而有围岩物质混入,而成矿流体与围岩发生的强烈水–岩反应也是白钨矿大量沉淀的重要机制。其高Mo和低Sr含量的特征,也符合岩浆–热液型矿床中白钨矿的特点。因此,综合努日矿床地质特征,白钨矿微量元素、Sr同位素地球化学特征及其对成矿流体来源、演化过程及矿床成因的指示,认为努日矿床属于斑岩–夕卡岩型矿床。
相似文献145.
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
146.
Combined Trace Element and Pb-Nd-Sr-O Isotope Evidence for Recycled Oceanic Crust (Upper and Lower) in the Iceland Mantle Plume 总被引:2,自引:0,他引:2
KOKFELT THOMAS FIND; HOERNLE KAJ; HAUFF FOLKMAR; FIEBIG JENS; WERNER REINHARD; GARBE-SCHONBERG DIETER 《Journal of Petrology》2006,47(9):1705-1749
We present the results of a comprehensive major element, traceelement and SrNdPbO isotopic study of post-glacialvolcanic rocks from the Neovolcanic zones on Iceland. The rocksstudied range in composition from picrites and tholeiites, whichdominate in the main rift systems, to transitional and alkalicbasalts confined to the off-rift and propagating rift systems.There are good correlations of rock types with geochemical enrichmentparameters, such as La/Sm and La/Yb ratios, and with long-termradiogenic tracers, such as SrNdPb isotope ratios,indicating a long-lived enrichment/depletion history of thesource region. 87Sr/86Sr vs 143Nd/144Nd defines a negative array.Pb isotopes define well-correlated positive arrays on both 206Pb/204Pbvs 207Pb/204Pb and 208Pb/204Pb diagrams, indicating mixing ofat least two major components: an enriched component representedby the alkali basalts and a depleted component represented bythe picrites. In combined SrNdPb isotopic spacethe individual rift systems define coherent mixing arrays withslightly different compositions. The enriched component hasradiogenic Pb (206Pb/204Pb > 19·3) and very similargeochemistry to HIMU-type ocean island basalts (OIB). We ascribethis endmember to recycling of hydrothermally altered upperbasaltic oceanic crust. The depleted component that is sampledby the picrites has unradiogenic Pb (206Pb/204Pb < 17·8),but geochemical signatures distinct from that of normal mid-oceanridge basalt (N-MORB). Highly depleted tholeiites and picriteshave positive anomalies in mantle-normalized trace element diagramsfor Ba, Sr, and Eu (and in some cases also for K, Ti and P),negative anomalies for Hf and Zr, and low 18Oolivine values(4·65·0) below the normal mantle range.All of these features are internally correlated, and we, therefore,interpret them to reflect source characteristics and attributethem to recycled lower gabbroic oceanic crust. Regional compositionaldifferences exist for the depleted component. In SW Icelandit has distinctly higher Nb/U (68) and more radiogenic 206Pb/204Pbratios (18·2818·88) compared with the NErift (Nb/U 47; 206Pb/204Pb = 18·0718·47).These geochemical differences suggest that different packagesof recycled oceanic lithosphere exist beneath each rift. A thirdand minor component with relatively high 87Sr/86Sr and 207Pb/204Pbis found in a single volcano in SE Iceland (Öræfajökullvolcano), indicating the involvement of recycled sediments inthe source locally. The three plume components form an integralpart of ancient recycled oceanic lithosphere. The slope in theuranogenic Pb diagram indicates a recycling age of about 1·5Ga with time-integrated Th/U ratios of 3·01. Surprisingly,there is little evidence for the involvement of North AtlanticN-MORB source mantle, as would be expected from the interactionof the Iceland plume and the surrounding asthenosphere in formof plumeridge interaction. The preferential samplingof the enriched and depleted components in the off-rift andmain rift systems, respectively, can be explained by differencesin the geometry of the melting regions. In the off-rift areas,melting columns are truncated deeper and thus are shorter, whichleads to preferential melting of the enriched component, asthis starts melting deeper than the depleted component. In contrast,melting proceeds to shallower depths beneath the main rifts.The longer melting columns also produce significant amountsof melt from the more refractory (lower crustal/lithospheric)component. KEY WORDS: basalts; trace element and Sr, Nd, Pb, O isotope geochemistry; Iceland plume; isotope ratios; oceanic crustal recycling; partial melting; plumeridge interaction 相似文献
147.
New palaeotemperature reconstructions have been obtained on the basis of oxygen isotopic analysis of 178 aragonitic shell samples taken from specimens of three ammonoid orders (and some corresponding families): Phylloceratida (Phylloceratidae), Lytoceratida (Tetragonitidae) and Ammonitida (Oppeliidae, Desmoceratidae, Silesitidae, Cleoniceratidae and Douvilleiceratidae). Those obtained from aragonite shells, secreted in the lower epipelagic and in the middle mesopelagic zones during coolest season (winter), range from 15.4 to 16.8 °C, and from 11.8 to 12.0 °C, respectively. Presumed spring/autumn palaeotemperatures obtained from aragonite shells, secreted apparently in the upper and lower epipelagic, upper and middle mesopelagic zones, are somewhat higher. Presumed summer palaeotemperatures, calculated apparently for the upper and lower epipelagic, and upper mesopelagic zones range from 19.4 to 21.7 °C, from 17.7 to 19.4 °C, and from 14.4 to 16.1 °C, respectively. The predominant part of investigated ammonoids from Madagascar inhabited the epipelagic zone, but some phylloceratid, tetragonitid and silesitid ammonoids preferred deeper, cooler conditions (upper-middle mesopelagic zone). The study supports the hypothesis that Madagascar was located in middle latitudes within the tropical-subtropical climatic zone during the early Albian. Available carbon and strontium isotope data allow us to assume a more or less expressed carbon and strontium isotope stratification of the water column in this region in the early Albian. On the basis of the stable isotope data, following partly Lukeneder (2015), two large ethological groups can be recognised mainly in mid-aged and adult ammonoids. Some ammonoids (group 1) preferred apparently mesopelagic conditions, and to a lesser degree the epipelagic zone, being mainly cool-requiring animals. However, a significant part of the isotopically investigated ammonoids (group 2) preferred, on the contrary, only epipelagic conditions, being mainly thermophilic dwellers. 相似文献
148.
江西相山铀矿田科学深钻3号孔在深部-700 m发现大量铅锌多金属矿化脉,垂向上呈"上铀下多金属"的分布特征。本文选取深部多金属矿脉主成矿阶段(S3)自形闪锌矿样品6件和不同阶段的毒砂、黄铁矿、方铅矿、方解石等样品12件,以及围岩全岩样品17件,进行了Rb、Sr同位素组成研究。结果表明:(1)由闪锌矿Rb-Sr等时线法确定的相山铀矿田深部多金属矿化形成于121. 0±3. 5Ma,与围岩火山岩存在较大时差,可能与晚于围岩的深部次火山有关。根据穿插关系,多金属矿化略晚于碱性交代铀矿化,但明显早于酸性交代铀矿化;(2)多金属矿化脉体中金属矿物的Rb和Sr含量分别介于0. 041×10~(-6)~1. 38×10-6和2. 35×10-6~23. 11×10-6之间,Sr同位素初始比值(87Sr/86Sr)i变化较大,介于0. 706114~0. 718814之间,平均值为0. 713579,暗示相山铀矿田深部多金属矿化的成矿物质主要来源于地壳。初始流体Sr同位素值(0. 718665)明显高于成矿时赋矿围岩(流纹英安岩为0. 714581,碎斑流纹岩为0. 714417)的Sr同位素组成,表明多金属成矿流体和物质并非来自围岩火山岩;(3)由早到晚阶段的(87Sr/86Sr)i呈明显降低的演化趋势,表明成矿流体演化过程中受到大气降水的不断稀释作用。相山矿田的铀矿和深部多金属矿化同形成于华南中生代板内伸展构造背景。 相似文献
149.
华南花岗岩物源成因特征与陆壳演化 总被引:15,自引:1,他引:15
华南不同时代的花岗岩按物质来源及成因可划分为:幔源(分异)系列:幔-壳混源(同熔)系列;壳源改造(重熔)系列和幔-壳混源碱性系列等四个不同的系列,简要阐述了划分四类系列的岩石学、地球化学的依据。侧重根据Sm-Nd、Rb-Sr同位素成分,以二元混合模型计算了花岗岩源区物质组成中,上壳和亏损地幔组份各占的比例。在此基础上探讨了不同物源成因系列花岗岩形成与华南陆壳演化的内在联系:东安、雪峰旋回褶皱系阶段花岗岩物源成因类型比较多样,有幔源(分异)系列、不成熟壳源、成熟壳源改造(重熔)系列等;加里东,海西期以陆壳改造(重熔)系列为主;印支、燕山期活化区(地洼)阶段,在地幔活化激发下,中国东部陆缘形成幔—壳混源(同熔)系列花岗岩和相应的火山岩;但沿内部断裂带,在壳下地幔热传输及构造作用下引起陆壳重熔,形成属于壳源改造(重熔)系列花岗岩。同位素的研究证明了:地洼阶段的构造-岩浆活动主要动力是来自壳下地幔的活化。 相似文献
150.
Aubry Vanderstraeten Steeve Bonneville Stefania Gili Jeroen de Jong Wendy Debouge Philippe Claeys Nadine Mattielli 《Geostandards and Geoanalytical Research》2020,44(2):307-329
Atmospheric dust is an integral component of the Earth system with major implications for the climate, biosphere and public health. In this context, identifying and quantifying the provenance and the processes generating the various types of dust found in the atmosphere is paramount. Isotopic signatures of Pb, Nd, Sr, Zn, Cu and Fe are commonly used as sensitive geochemical tracers. However, their combined use is limited by the lack of (a) a dedicated chromatographic protocol to separate the six elements of interest for low‐mass samples and (b) specific reference materials for dust. Indeed, our work shows that USGS rock reference materials BHVO‐2, AGV‐2 and G‐2 are not applicable as substitute reference materials for dust. We characterised the isotopic signatures of these six elements in dust reference materials ATD and BCR‐723, representatives of natural and urban environments, respectively. To achieve this, we developed a specific procedure for dust, applicable in the 4–25 mg mass range, to separate the six elements using a multi‐column ion‐exchange chromatographic method and MC‐ICP‐MS measurements. 相似文献