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61.
Abstract  Abundant mafic microgranular enclaves (MMEs) extensively distribute in granitoids in the Gangdisê giant magmatic belt, within which the Qüxü batholith is the most typical MME‐bearing pluton. Systematic sampling for granodioritic host rock, mafic microgranular enclaves and gabbro nearby at two locations in the Qüxü batholith, and subsequent zircon SHRIMP II U‐Pb dating have been conducted. Two sets of isotopic ages for granodioritic host rock, mafic microgranular enclaves and gabbro are 50.4±1.3 Ma, 51.2±1.1 Ma, 47.0±1 Ma and 49.3±1.7 Ma, 48.9±1.1 Ma, 49.9±1.7 Ma, respectively. It thus rules out the possibilities of mafic microgranular enclaves being refractory residues after partial melting of magma source region, or being xenoliths of country rocks or later intrusions. Therefore, it is believed that the three types of rocks mentioned above likely formed in the same magmatic event, i.e., they formed by magma mixing in the Eocene (c. 50 Ma). Compositionally, granitoid host rocks incline towards acidic end member involved in magma mixing, gabbros are akin to basic end member and mafic microgranular enclaves are the incompletely mixed basic magma clots trapped in acidic magma. The isotopic dating also suggested that huge‐scale magma mixing in the Gangdisê belt took place 15–20 million years after the initiation of the India‐Asia continental collision, genetically related to the underplating of subduction‐collision‐induced basic magma at the base of the continental crust. Underplating and magma mixing were likely the main process of mass‐energy exchange between the mantle and the crust during the continental collision, and greatly contributed to the accretion of the continental crust, the evolution of the lithosphere and related mineralization beneath the portion of the Tibetan Plateau to the north of the collision zone.  相似文献   
62.
63.
Timing of folding is usually dated indirectly, with limited isotopic dating studies reported in the literature. The present study investigated the timing of intracontinental, multi-stage folding in Upper Proterozoic sandstone, limestone, and marble near Beijing, North China, and adjacent regions. Detailed field investigations with microstructural, backscattered electron (BSE) images and electron microprobe analyses indicate that authigenic muscovite and sericite crystallized parallel to stretching lineations/striations or along thin flexural-slip surfaces, both developed during the complex deformation history of the study area, involving repeated compressional, extensional and strike-slip episodes. Muscovite/sericite separates from interlayer-slip surfaces along the limbs and from dilatant sites in the hinges of folded sandstones yield muscovite 40Ar/39Ar plateau ages of ∼158–159 Ma, whereas those from folded marble and limestone samples yield ages of 156 ± 1 Ma. Muscovite from thin flexural-slip planes on fold limbs and hinges yields ages within analytical error of ∼155–165 Ma. Further muscovite samples collected from extensionally folded limestone and strike-slip drag folds yield younger ages of 128–125 Ma with well-defined plateaus. To assess the potential influence of the detrital mica component of the host rock on the age data, two additional muscovite samples were investigated, one from a folded upper Proterozoic–Cambrian sandstone outside the Western Hills of Beijing and one from a folded sandstone sampled 20 cm from folding-related slip planes. Muscovite separates from these samples yield significantly older ages of 575 ± 2 Ma and 587 ± 2 Ma, suggesting that the timing of folding can be directly determined using the 40Ar/39Ar method. This approach enables the identification and dating of distinct deformation events that occur during multi-stage regional folding. 40Ar/39Ar dating can be used to constrain the timing of muscovite and sericite growth at moderate to low temperatures (<400 °C) during folding, yielding well-defined plateau ages and thereby the age of deformation in the upper crust.  相似文献   
64.
滇东北火德红铅锌矿床地球化学特征与成矿机制分析   总被引:1,自引:0,他引:1  
文章通过研究滇东北火德红铅锌矿床岩石地球化学和S、Pb同位素地球化学特征,分析其成矿金属和成矿流体来源,进而对其成矿机制进行探讨。围岩主量与微量元素分析结果表明,火德红铅锌矿床为后生热液矿床,铅锌等成矿金属物质随热液进入赋矿围岩,结合围岩蚀变特征判断,其应属中_低温热液成因;闪锌矿与黄铁矿的δ34S主要分布在-17‰~-11.4‰,其S源极可能来自生物成因硫酸盐还原,与川滇黔地区铅锌矿的S同位素来源(总体来自海水硫酸盐热化学还原)有着明显的不同;矿石硫化物的Pb同位素比值变化范围较窄,均为正常Pb;Pb同位素主要来自于上地壳,有少量岩浆物质混入。上述特征表明火德红铅锌矿床为构造和岩性共同控制的后生热液型矿床,其成矿机制与典型MVT型铅锌矿相似。  相似文献   
65.
宝山铜铅锌多金属矿床是湖南重要的铅锌生产基地。矿床内矽卡岩型铜(钼)矿化受侏罗纪花岗闪长斑岩的控制,而主要的铅锌矿体则产于远离岩体的碳酸盐地层中,且缺乏可靠的矿化年龄限制。为了查明宝山铅锌矿体与花岗闪长斑岩之间的成因关系,文章对宝山花岗岩类中浸染状黄铁矿的硫同位素和钾长石的铅同位素,以及铅锌矿石萤石脉石的流体包裹体进行了测试和研究,并与前人报道的铅锌硫化物矿石的硫、铅同位素进行了对比,尝试为宝山铅锌矿化的物质来源及成因提供依据。研究表明,花岗闪长斑岩中浸染状黄铁矿的δ34S值为+1.5‰~+3.5‰,与铅锌矿石硫化物(方铅矿、闪锌矿及黄铁矿)相一致;同时,花岗岩类中钾长石的铅同位素组成206Pb/204Pb、207Pb/204Pb和208Pb/204Pb分别为18.4789~18.7668、15.6835~15.7220和38.7903~39.1035,具有壳源的特征,且与铅锌矿石硫化物的铅同位素分布范围相吻合。宝山矿床的硫、铅同位素特征表明,花岗闪长斑岩应是铅锌矿化的主要硫源及金属来源。宝山矿床铅锌矿石萤石中的流体包裹体具有低温(130~150℃)、低盐度(8%)的特征,可能是岩浆热液演化到晚期的产物。结合已有的有关资料加以对比和分析,研究认为,宝山铅锌矿床的成矿物质应来源于花岗闪长岩的岩浆期后热液,在热液演化晚期迁移到远端地层中沉淀,形成了宝山的主要铅锌矿体。  相似文献   
66.
华北陆块南缘外方山店房金矿区内出露后沟、水漉塘和店房钾长花岗斑岩体(脉),其与隐爆角砾岩筒及金矿化有密切的空间关系。为查明钾长花岗斑岩体的侵位时代、岩石成因和源区性质,本次开展了锆石U-Pb定年、锆石Hf同位素及岩石地球化学分析等研究。结果表明岩体具有高硅、高钾、富铝、低镁的特征,属钾玄岩系列Ⅰ型花岗岩,轻重稀土元素分馏明显,具有弱的Eu负异常,岩石富集Rb、K、Ba等,亏损Nb、Ta、Sr、P、Ti等元素。锆石具有核—边结构,其中锆石边SHRIMP U-Pb年龄142.6±2.1Ma(MSWD=1.4),_(εHf)(t)=-23.0~-13.8,两阶段模式年龄主要集中于2075~2652 Ma;锆石核LA-ICPMS U-Pb年龄可分为两组,即2169~2336Ma和1732~1881Ma,Hf同位素组成可分为两组,_(εHf)(t)分别集中于-13.1~-4.8和-4.5~3.7,模式年龄主要集中于2376~2805Ma。表明钾长花岗斑岩体形成于142.6±2.1Ma的早白垩世早期,岩浆可能由2169~2336Ma的古老下地壳新太古代太华群部分熔融而成,并有地幔组分参与,岩浆在上升或定位过程中捕获了1732~1881Ma熊耳群火山岩的锆石。结合区域构造背景认为,该岩体是早白垩世古太平洋板块向欧亚大陆俯冲致使华北陆块岩石圈减薄伸展而引起的岩浆活动的产物。  相似文献   
67.
Iodine enrichment in the Atacama Desert of northern Chile is widespread and varies significantly between reservoirs, including nitrate-rich “caliche” soils, supergene Cu deposits and marine sedimentary rocks. Recent studies have suggested that groundwater has played a key role in the remobilization, transport and deposition of iodine in Atacama over scales of millions-of-years. However, and considering that natural waters are also anomalously enriched in iodine in the region, the relative source contributions of iodine in the waters and its extent of mixing remain unconstrained. In this study we provide new halogen data and isotopic ratios of iodine (129I/I) in shallow seawater, rivers, salt lakes, cold and thermal spring water, rainwater and groundwater that help to constrain the relative influence of meteoric, marine and crustal sources in the Atacama waters. Iodine concentrations in surface and ground waters range between 0.35 μM and 26 μM in the Tarapacá region and between 0.25 μM and 48 μM in the Antofagasta region, and show strong enrichment when compared with seawater concentrations (I = ∼0.4 μM). In contrast, no bromine enrichment is detected (1.3–45.7 μM for Tarapacá and 1.7–87.4 μM for Antofagasta) relative to seawater (Br = ∼600 μM). These data, coupled to the high I/Cl and low Br/Cl ratios are indicative of an organic-rich sedimentary source (related with an “initial” fluid) that interacted with meteoric water to produce a mixed fluid, and preclude an exclusively seawater origin for iodine in Atacama natural waters. Iodine isotopic ratios (129I/I) are consistent with halogen chemistry and confirm that most of the iodine present in natural waters derives from a deep initial fluid source (i.e., groundwater which has interacted with Jurassic marine basement), with variable influence of at least one atmospheric or meteoric source. Samples with the lowest isotopic ratios (129I/I from ∼215 to ∼1000 × 10−15) strongly suggest mixing between the groundwater and iodine storage in organic-rich rocks (with variable influence of volcanic fluids) and pre-anthropogenic meteoric water, while samples with higher values (∼2000–93,700 × 10−15) indicate the input of anthropogenic meteoric fluid. Taking into account the geological, hydrologic and climatic features of the Atacama region, we propose that the mean contribution of anthropogenic 129I is associated with 129I releases during nuclear weapon tests carried out in the central Pacific Ocean until the mid 1990's (129I/I = ∼12,000 × 10−15). This source reflects rapid redistribution of this radioisotope on a global scale. Our results support the notion of a long-lived continental iodine cycle in the hyperarid margin of western South America, which is driven by local hydrological and climate conditions, and confirm that groundwater was a key agent for iodine remobilization and formation of the extensive iodine-rich soils of Atacama.  相似文献   
68.
大湖塘矿集区位于赣西北九岭成矿带西北部位,区内燕山期岩浆岩侵入活动及成矿作用强烈。大湖塘燕山期岩浆岩形成时间分布在130.3 Ma~151.4 Ma之间,可划分为三次侵入:130.3 Ma~134.3 Ma、140.4 Ma~144.4 Ma、146.4 Ma~151.4 Ma;在144.4 Ma~146.4 Ma之间,岩浆活动处于休宁阶段。区内燕山期岩浆岩与矿床在形成时间上十分接近,空间关系上相互依存,并显示特定的分布格局。根据区内矿床的分布特点、产出位置、成矿时间、燕山期花岗岩与矿床的相关性等特征,可将大湖塘矿集区由北向南依次划分为W、Mo—W、Mo、Cu、Pb、Zn—Cu、Pb、Zn、Au、Ag三个成矿系列,并提出了"北钨南铜"的找矿观点。区内双桥山群与成矿,燕山期岩浆岩的起源,矿床等间距分布,以及重力勘探方面的研究应加强。  相似文献   
69.
在弯道水槽中开展6组试验,分别用非黏性土及黏性土填筑河床,研究相同水力作用下近岸河床组成对黏性岸坡崩塌的影响规律。研究发现,在试验给定的岸坡及河床组成情况下,非黏性河床凹冲凸淤且总体表现为淤积,近岸河床及凹岸岸坡冲刷强度大,凸岸附近床面上泥沙掺混较明显;黏性河床及凹岸岸坡均被冲刷,河床主流区冲刷强度比近岸河床及凹岸岸坡大。相较于黏性河床,非黏性河床近凹岸处较易冲刷,水流结构重新调整,凹岸坡脚处水流流速及紊动能可增至2倍左右,环流强度可增至11倍,加速了岸坡崩塌及崩塌体的分解输移;非黏性河床近凹岸坡脚处变形以及凹岸岸坡崩塌量均相对较大,岸坡崩塌强度为河床淤积强度的2~4倍,崩塌物质可充分补给河床的泥沙来源;经水力冲刷后非黏性河床组成情况下形成的河道滩槽高差相对较小,河道横断面相对宽浅。  相似文献   
70.
以西藏冈底斯中段西侧桑桑花岗质岩体为对象,进行了系统的年代学、元素地球化学和锆石Hf同位素组成研究,据此阐明了岩体成因,并探讨了其构造意义。锆石LA-ICP-MS U-Pb定年表明,桑桑花岗质岩体的成岩年龄为49~54 Ma。化学组成上,岩体具有亚碱、准铝、贫磷的特征(A/NKC1.10,P_2O_50.20%),属钙碱性I型花岗岩类。岩体富Cs、Rb、Ba、Th、U、K、Pb和轻稀土,贫Nb、Ta、P与Ti,表现出弧岩浆岩的地球化学特征。岩体的锆石εHf(t)值变化较大,散布于正值与负值之间(=-4.24~+5.49),指示其形成存在不同来源物质的贡献。综合分析表明,桑桑花岗质岩体起源于初生地壳的部分熔融,但在成岩过程中有古老地壳组分的参与。结合区域地质背景,笔者认为这一古老地壳组分最可能来自印亚碰撞过程中俯冲下插的印度地壳,由此说明印度-欧亚大陆碰撞的起始时间应早于54 Ma。  相似文献   
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