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991.
王毅  崔凤娟 《海洋与湖沼》2015,46(2):241-247
本文通过分析RAMA印度洋观测浮标系统锚系ADCP实测资料,对赤道中印度洋上层海流季节变化进行了研究。研究结果表明,0°,80.5°E纬向流垂向剖面呈现上150m层一致的东向流,而经向流在100m以浅呈现表层向北次表层向南的翻转流结构。赤道中印度洋上层纬向流季节信号被半年周期的东向射流Wyrtki Jets(WJs)所控制。WJs发生于季风方向转换的季节,4—5月份较弱,10—11月份较强。赤道中印度洋上层经向流年周期信号显著。北半球夏季与冬季分别出现风应力旋度驱动的Sverdrup南向流与北向流。本文结论为赤道中印度洋上层环流季节变化特征的研究提供了观测角度的支持。  相似文献   
992.
长波区间太阳辐射对气候模拟的影响   总被引:1,自引:0,他引:1       下载免费PDF全文
长波区间的太阳辐射在气候模式中往往被忽略。利用国家气候中心BCC_AGCM2.0.1大气环流模式,采用矩阵算子辐射传输算法,研究了长波区间太阳辐射对气候模式辐射通量和温度模拟结果的影响。结果表明,以ISCCP和CERES辐射资料为标准,考虑长波区间太阳辐射后,长波区间晴空大气地表向下辐射通量平均误差减小2.05 W/m2,均方根误差减少1.29 W/m2;长波区间晴空大气模式顶向上辐射通量平均误差减小0.70 W/m2,均方根误差减小0.21 W/m2;长波区间有云大气地表向下辐射通量平均误差减小1.38 W/m2,均方根误差减小1.03 W/m2;长波区间有云大气模式顶向上辐射通量平均误差减小0.99 W/m2,均方根误差减小0.30 W/m2。以ECMWF再分析资料为标准,考虑长波区间太阳辐射后,赤道地区上对流层—下平流层区域温度的冷偏差得到改善,对流层顶温度平均误差减小0.27 K,均方根误差减小0.25 K。  相似文献   
993.
目前,胶东金矿成矿流体研究主要集中在成矿流体的来源及其成矿过程研究,但是对于其侵位前的物化状态及分异演化研究尚浅。该文提出胶东金矿矿集区幔源成矿流体深部演化的一种形成机制,并认为胶东金矿幔源成矿流体在侵位前发生了富集作用。正是由于幔源成矿流体的富集作用才使得胶东地区形成现在规模、品位的金矿。胶东金矿幔源成矿流体的侵位机制主要受华北东部构造转折体制制约。根据胶东地区金矿幔源成矿流体分异演化特征、构造特征及现有深部探测实例表明:胶东地区在1000m以下极有可能存在另一个大型金矿带。  相似文献   
994.
陈伟  刘泰  佘雅文  付广裕 《地震》2021,41(4):121-135
基于黏弹性球体位错理论, 联合陆地和海底同震GPS数据以及日本本岛330个陆地GPS站点5~10年的震后数据, 反演了日本MW9.0地震的断层滑动模型, 提升了断层滑动分布在细节上的合理性。 首先, 基于日本本岛330个陆地GPS站点震前2年和震后10年的连续观测数据, 获取了日本MW9.0地震震后5~10年的年平均位移, 该时段的位移几乎完全由地幔黏弹性松弛效应引起; 接着, 利用黏弹性球体位错理论对震后5~10年的位移进行反复拟合, 确定了日本MW9.0地震震源及周边地区的地幔黏滞性系数最优解(9.0×1018 Pa·s)。 然后, 联合同震和震后位移数据, 引入黏弹性位错格林函数, 反演了2011年日本MW9.0地震的断层滑动分布。 结果表明, 该地震同震破裂的最大值达到了62.72 m, 同震滑动的总地震矩为4.48×1022 Nm, 相应的矩震级为MW9.03。 由于黏弹性松弛效应引起的震后位移中包含了同震破裂的信息, 基于黏弹性球体地震位错理论, 联合同震和震后位移数据反演断层同震破裂, 有效提高了日本MW9.0地震断层滑动分布的可靠性。 最后, 本文提出的反演方法为同震观测结果缺乏的大地震震后科考提供了理论支撑: 在大地震发生之后, 即使在同震期间没有足够的观测数据, 也可以在震后通过对震源区的加密观测积累的震后数据, 使用本文提出的反演方法优化同震断层滑动模型。  相似文献   
995.
An improved understanding of postseismic crustal deformation following large subduction earthquakes may help to better understand the rheological properties of upper mantle and the slip behavior of subduction interface. Here we construct a three-dimensional viscoelastic finite element model to study the postseismic deformation of the 2014 MW8.1 Iquique, Chile earthquake. Elastic units in the model include the subducting slab, continental and oceanic lithospheres. Rheological units include the mantle wedge, the oceanic asthenosphere and upper mantle. We use a 2 ​km thick weak shear zone attached to the subduction fault to simulate the time-dependent stress-driven afterslip. The viscoelastic relaxation in the rheological units is represented by the Burgers rheology. We carry out grid-searches on the shear zone viscosity, thickness and viscosity of the asthenosphere, and they are determined to be 1017 ​Pa ​s, 110 ​km and 2 ​× ​1018 ​Pa ​s, respectively. The stress-driven afterlsip within the first two years is up to ~47 ​cm and becomes negligible after two years (no more than 5 ​cm/yr). Our results suggest that a thin, low-viscosity oceanic asthenosphere together with a weak shear zone attached to the fault are required to better reproduce the observed postseismic deformation.  相似文献   
996.
The Maoniuping REE deposit, located about 22 km to the southwest of Mianning, Sichuan Province, is the second largest light REE deposit in China, subsequent to the Bayan Obo Fe-Nb-REE deposit in the Inner Mongolia Autonomous Region. Tectonically, it is located in the transitional zone between the Panxi rift and the Longmenshan-Jinpingshan orogenic zone. It is a carbonatite vein-type deposit hosted in alkaline complex rocks. The bastnaesite-barite, bastnaesite-calcite, and bastnaesite-microcline lodes are the main three types of REE ore lodes. Among these, the first lode is distributed most extensively and its REE mineralization is the strongest. Theδ34Sv-CDT values of the barites in the ore of the deposit vary in a narrow range of +5.0 to +5.1‰in the bastnaesite-calcite lode and +3.3 to +5.9‰in the bastnaesite-barite lode, showing the isotopic characteristics of magma-derived sulfur. Theδ13Cv-PDB values and theδ518OV-SMOW values in the bastnaesite-calcite lode range from -3.9 to -6.9‰and from +7.3 to +9.7‰, respectively, which fall into the range of "primary carbonatites", showing that carbon and oxygen in the ores of the Maoniuping deposit were derived mainly from a deep source. Theδ13Cv-PDB values of fluid inclusions vary from -3.0 to -5.6‰, with -3.0 to -4.0‰in the bastnaesite-calcite lode and -3.0 to -5.6‰in the bastnaesite-barite lode, which show characteristics of mantle-derived carbon. TheδDv-SMOW values of fluid inclusions range from -57 to -88‰, with -63 to -86‰in the bastnaesite-calcite lode and -57 to -88‰in the bastnaesite-barite lode, which show characteristics of mantle-derived hydrogen. Theδ18OH2OV-SMOW values vary from +7.4 to +8.6‰in the bastnaesite calcite lode, and +6.7 to +7.8‰in the bastnaesite-barite lode, almost overlapping the range of +5.5 to +9.5‰for magmatic water. The 4He content, R/Ra ratios are (13.95 to 119.58×10-6 (cm3/g)STP and 0.02 to 0.11, respectively, and 40Ar/36Ar is 313±1 to 437±2. Considering the 4He increase caused by high contents of radioactive elements, a mantle-derived fluid probably exists in the inclusions in the fluorite, calcite and bastnaesite samples. The Maoniuping deposit and its associated carbonatite-alkaline complex were formed in 40.3 to 12.2 Ma according to K-Ar and U-Pb data. All these data suggest that large quantities of mantle fluids were involved in the metallogenic process of the Maoniuping REE deposit through a fault system.  相似文献   
997.
This paper presents field, geochemical and isotopic (Sr, Nd,Pb) results on basalts from the Antipodes, Campbell and ChathamIslands, New Zealand. New 40Ar/39Ar age determinations alongwith previous K–Ar dates reveal three major episodes ofvolcanic activity on Chatham Island (85–82, 41–35,5 Ma). Chatham and Antipodes samples comprise basanite, alkaliand transitional basalts that have HIMU-like isotopic (206Pb/204Pb>20·3–20·8, 87Sr/86Sr <0·7033,143Nd/144Nd >0·5128) and trace element affinities(Ce/Pb 28–36, Nb/U 34–66, Ba/Nb 4–7). Thegeochemistry of transitional to Q-normative samples from CampbellIsland is explained by interaction with continental crust. Thevolcanism is part of a long-lived (100 Myr), low-volume, diffusealkaline magmatic province that includes deposits on the Northand South Islands of New Zealand as well as portions of WestAntarctica and SE Australia. All of these continental areaswere juxtaposed on the eastern margin of Gondwanaland at >83Ma. A ubiquitous feature of mafic alkaline rocks from this regionis their depletion in K and Pb relative to other highly incompatibleelements when normalized to primitive mantle values. The inversionof trace element data indicates enriched mantle sources thatcontain variable proportions of hydrous minerals. We proposethat the mantle sources represent continental lithosphere thathost amphibole/phlogopite-rich veins formed by plume- and/orsubduction-related metasomatism between 500 and 100 Ma. Thestrong HIMU signature (206Pb/204Pb >20·5) is consideredto be an in-grown feature generated by partial dehydration andloss of hydrophile elements (Pb, Rb, K) relative to more magmaphileelements (Th, U, Sr) during short-term storage at the base ofthe lithosphere. KEY WORDS: continental alkaline basalts; lithospheric mantle, mantle metasomatism; New Zealand; OIB, HIMU; Sr, Nd and Pb isotopes; West Antarctica  相似文献   
998.
The Neoproterozoic Aries kimberlite was emplaced in the centralKimberley Basin, Western Australia, as a N–NNE-trendingseries of three diatremes infilled by lithic-rich kimberlitebreccias. The breccias are intruded by hypabyssal macrocrysticphlogopite kimberlite dykes that exhibit differentiation toa minor, high-Na–Si, olivine–phlogopite–richteritekimberlite, and late-stage macrocrystic serpentine–diopsideultramafic dykes. Mineralogical and geochemical evidence suggeststhat the high-Na–Si, olivine–phlogopite–richteritekimberlite was derived from the macrocrystic phlogopite kimberliteas a residual liquid following extended phlogopite crystallizationand the assimilation of country rock sandstone, and that themacrocrystic serpentine–diopside ultramafic dykes formedas mafic cumulates from a macrocrystic phlogopite kimberlite.Chemical zonation of phlogopite–biotite phenocrysts indicatesa complex magmatic history for the Aries kimberlite, with theearly inheritance of a range of high-Ti phlogopite–biotitexenocrysts from metasomatized mantle lithologies, followed bythe crystallization of a population of high-Cr phlogopite phenocrystswithin the spinel facies lithospheric mantle. A further oneto two phlogopite–biotite overgrowth rims of distinctcomposition formed on the phlogopite phenocrysts at higher levelsduring ascent to the surface. Ultra-violet laser 40Ar/39Ar datingof mica grain rims yielded a kimberlite eruption age of 815·4± 4·3 Ma (95% confidence). 40Ar/39Ar laser profilingof one high-Ti phlogopite-biotite macrocryst revealed a radiogenic40Ar diffusive loss profile, from which a kimberlite magma ascentduration from the spinel facies lithospheric mantle was estimated(assuming an average kimberlite magma temperature of 1000°C),yielding a value of 0·23–2·32 days for thenorth extension lobe of the Aries kimberlite. KEY WORDS: 40Ar/39Ar; diamond; kimberlite; mantle metasomatism; phlogopite–biotite  相似文献   
999.
Major- and trace-element data on the constituent minerals ofgarnet peridotite xenoliths hosted in early Paleozoic (457–500Ma) kimberlites and Neogene (16–18 Ma) volcanic rockswithin the North China Craton are compared with those from thepre-pilot hole of the Chinese Continental Scientific DrillingProject (CCSD-PP1) in the tectonically exhumed Triassic (220Ma) Sulu ultrahigh-pressure (UHP) terrane along its southernmargin. P–T estimates for the Paleozoic and Neogene peridotitexenoliths reflect different model geotherms corresponding tosurface heat flows of 40 mW/m2 (Paleozoic) and 80 mW/m2 (Neogene).Garnet peridotite xenoliths or xenocrysts from the Paleozoickimberlites are strongly depleted, similar to peridotites fromother areas of cratonic mantle, with magnesium olivine (meanFo92.7), Cr-rich garnet and clinopyroxene with high La/Yb. Garnet(and spinel) peridotite xenoliths hosted in Neogene basaltsare derived from fertile mantle; they have high Al2O3 and TiO2contents, low-Mg-number olivine (mean Fo89.5), low-Cr garnetand diopside with flat rare earth element (REE) patterns. Thedifferences between the Paleozoic and Neogene xenoliths suggestthat a buoyant refractory lithospheric keel present beneaththe eastern North China Craton in Paleozoic times was at leastpartly replaced by younger, hotter and more fertile lithosphericmantle during Mesozoic–Cenozoic times. Garnet peridotitesfrom the Sulu UHP terrane have less magnesian olivine (Fo91.5),and lower-Cr garnet than the Paleozoic xenoliths. The diopsideshave low heavy REE (HREE) contents and sinusoidal to light REE(LREE)-enriched REE patterns. These features, and their highMg/Si and low CaO and Al2O3 contents, indicate that the CCSD-PP1peridotites represent a moderately refractory mantle protolith.Details of mineral chemistry indicate that this protolith experiencedcomplex metasomatism by asthenosphere-derived melts or fluidsin Mesoproterozoic, and subsolidus re-equilibration involvingfluids/melts derived from the subducted Yangtze continentalcrust during UHP metamorphism in the early Mesozoic. Tectonicextension of the subcontinental lithospheric mantle of the NorthChina Craton and exhumation of the Sulu UHP rocks in the earlyMesozoic induced upwelling of the asthenosphere. Peridotitessampled by the Neogene basalts represent newly formed lithospherederived by cooling of the upwelling asthenospheric mantle inJurassic–Cretaceous and Paleogene time. KEY WORDS: garnet peridotite xenoliths; North China Craton; lithospheric thinning; Sulu UHP terrane; UHP lithosphere evolution; mantle replacement  相似文献   
1000.
The spinel–garnet transition in Cr/Al-enriched peridotiticbulk compositions is known from experimental investigationsto occur at 20–70 kbar, within the pressure range sampledby kimberlites. We show that the Cr2O3–CaO compositionsof concentrate garnets from kimberlite have maximum Cr/Ca arrayscharacterized by Cr2O3/CaO 0·96–0·81, andinterpret the arrays as primary evidence of chromite–garnetcoexistence in Cr-rich harzburgitic or lherzolitic bulk compositionsderived from depth within the lithosphere. Under Cr-saturatedconditions on a known geotherm, each Cr/Ca array implicitlydelineates an isobar inside a garnet Cr2O3–CaO diagram.This simplification invites a graphical approach to calibratean empirical Cr/Ca-in-pyrope barometer. Carbonaceous chromite–garnetharzburgite xenoliths from the Roberts Victor kimberlite tightlybracket a graphite–diamond constraint (GDC) located atCr2O3 = 0·94CaO + 5·0 (wt %), representing a pivotalcalibration corresponding to 43 kbar on a 38 mW/m2 conductivegeotherm. Additional calibration points are established at 14,17·4 and 59·1 kbar by judiciously projecting garnetcompositions from simple-system experiments onto the same geotherm.The garnet Cr/Ca barometer is then simply formulated as follows(in wt %):
if Cr2O3 0·94CaO + 5, then P38 (kbar) = 26·9+ 3·22Cr2O3 – 3·03CaO, or
if Cr2O3 <0·94CaO + 5, then P38 (kbar) = 9·2+ 36[(Cr2O3+ 1·6)/(CaO + 7·02)].
A small correction to P38 values, applicable for 35–48mW/m2 conductive geotherms, is derived empirically by requiringconventional thermobarometry results and garnet concentratecompositions to be consistent with the presence of diamondsin the Kyle Lake kimberlite and their absence in the Zero kimberlite.We discuss application of the P38 barometer to estimate (1)real pressures in the special case where chromite–garnetcoexistence is known, (2) minimum pressures in the general casewhere Cr saturation is unknown, and (3) the maximum depth ofdepleted lithospheres, particularly those underlying Archaeancratons. A comparison with the PCr barometer of Ryan et al.(1996, Journal of Geophysical Research 101, 5611–5625)shows agreement with P38 at 55 ± 2 kbar, and 6–12%higher PCr values at lower P38. Because the PCr formulationsystematically overestimates the 43 kbar value of the GDC by2–6 kbar, we conclude that the empirical Cr/Ca-in-garnetbarometer is preferred for all situations where conductive geothermsintersect the graphite–diamond equilibrium. KEY WORDS: Cr-pyrope; chromite; P38 barometer; mantle petrology; lithosphere thickness  相似文献   
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