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71.
Carbon isotopic composition of marine carbonates is a record for various important geological events in the process of earth development and evolution. The carbonates of Carboniferous, Permian and Triassic, as the transition from Paleozoic to Mesozoic-Cenozoic have very high 13C value. Taking this as the main point, and combined with the oxygen, strontium isotopic composition in carbonates, distribution of carbonate basin area through geologic time, the correlation of carbon isotopic composition of marine carbonates to sea level change, organic carbon burial flux, exchange of CO2 content in atmosphere and ocean, and long cycle evolution of the earth ecosystems were approached. The results are shown as follows: ①The interval of 13C >3‰ during Phanerozoic was concentrated in Carboniferous, Permian and the beginning of Triassic, but the beginning of Triassic was characterized by higher frequency and larger fluctuations in 13C value during a short time, whereas the Carboniferous-Permian presented a continuously stable high 13C value, indicating a larger amount of organic carbon accumulation in this time interval. Relatively high 18O values during this time was also observed, showing a long time of glaciations and cold climate, which suggest a connection among rapid organic carbon burial, cold climate, as well as pCO2 and pO2 states of atmosphere. ②The over consumption of atmosphere CO2 by green plants during the time with high 13C of seawater forced CO2 being transferred from ocean to atmosphere for the balance, but the decrease in the seawater amount and water column pressure caused by the global cooling could weaken dissolution capacity of CO2 in seawater and carbon storage of marine carbonates, and also reduce the carbonate sedimentary rate and decrease the carbonate basin area globally from Devonian to Carboniferous and Permian. During the middle-late Permian carbonate was widely replaced by siliceous sediments even though in shallow carbonate platform, which resulted in the decrease of marine invertebrates, suggesting the Permian chert event should be global. ③The Phanerozoic 87Sr/86Sr trend of seawater showed a sharp fall in Permian and drop to a minimum at the end of the Permian, indicting input of strontium from the submarine hydrothermal systems (mantle flux). Such process should accompany with a supplement of CO2 from deep earth to atmosphere and ocean system, but the process associated with widespread volcanism and rises of earth’s surface temperature pricked up the mass extinction during the time of end Permian. ④Cold climate and increase of continental icecap volume, the amalgamation of northern Africa and Laurentia continentals were the main reasons responsible for the sea level drop, but the water consumption result from the significantly increased accumulation of organic carbon should also be one of the reasons for the sea level drop on the order of tens of meters. ⑤The mass extinction at the end Permian was an inevitable event in the process of earth system adjustment. It was difficult for marine invertebrates to survive because of the continuously rapid burial of organic carbon, and of the decrease of sea water amount and its dissolution ability to CO2. At last, at the end of Paleozoic, the supplement of CO2 to atmosphere and ocean by widely magma activities resulted in a high temperature of earth surface and intensified mass extinction.  相似文献   
72.
本文对越南西北部Phan Si Pan地区变质地体中的一个Ngoi Chi片麻岩进行了锆石CL内部结构分析、LA-(MC)-ICP-MS锆石U-Pb定年和Hf同位素分析。CL图象和Th/U比值特征显示该片麻岩样品中的锆石主要为岩浆锆石,有少量窄的变质边。岩浆锆石的年龄为~2.9 Ga,表明该样品是越南西北部Phan Si Pan地区的基底岩石。它们的εHf(t)值为–4.70±0.92,二阶段Hf模式年龄为~3.5 Ga,表明其为更古老的(3.5 Ga)冥太古代地壳物质部分熔融作用形成。变质边部锆石给出了~1.8 Ga的年龄,表明变质作用发生在古元古代早期,Phan Si Pan地区在这一时期可能经历了一次重要的构造热事件。  相似文献   
73.
We evaluate the performance of a hand‐held XRF (HHXRF) spectrometer for the bulk analysis of iron meteorites. Analytical precision and accuracy were tested on metal alloy certified reference materials and iron meteorites of known chemical composition. With minimal sample preparation (i.e., flat or roughly polished surfaces) HHXRF allowed the precise and accurate determination of most elements heavier than Mg, with concentrations > 0.01% m/m in metal alloy CRMs, and of major elements Fe and Ni and minor elements Co, P and S (generally ranging from 0.1 to 1% m/m) in iron meteorites. In addition, multiple HHXRF spot analyses could be used to determine the bulk chemical composition of iron meteorites, which are often characterised by sulfide and phosphide accessory minerals. In particular, it was possible to estimate the P and S bulk contents, which are of critical importance for the petrogenesis and evolution of Fe‐Ni‐rich liquids and iron meteorites. This study thus validates HHXRF as a valuable tool for use in meteoritics, allowing the rapid, non‐destructive (a) identification of the extraterrestrial origin of metallic objects (i.e., archaeological artefacts); (b) preliminary chemical classification of iron meteorites; (c) identification of mislabelled/unlabelled specimens in museums and private collections and (d) bulk analysis of iron meteorites.  相似文献   
74.
利用 LA ICP MS 锆石 U Pb 法,测得与成矿有关的青海祁漫塔格地区虎头崖矿床Ⅵ矿带花岗岩的成岩年龄为(233.6±1.8)Ma(MSWD=1.2,n=17)。地球化学特征显示:花岗岩属高钾钙碱性、弱过铝质花岗岩;样品的稀土元素组成以总体右倾,轻、重稀土分异明显和具明显的负铕异常为特征;微量元素具有富集 Rb、Th、U、La、Nd 等大离子亲石元素,亏损 Ba、Sr、Nb、P、Ti 等元素的特点。Sr Nd 同位素组成特征显示,花岗岩的源区可能是富集岩石圈地幔。初步研究认为,虎头崖矿床Ⅵ矿带花岗岩可能形成于中、晚三叠世碰撞后碰撞的构造背景下。  相似文献   
75.
利用 LA ICP MS 锆石 U Pb 法,测得与成矿有关的青海祁漫塔格地区虎头崖矿床Ⅵ矿带花岗岩的成岩年龄为(233.6±1.8)Ma(MSWD=1.2,n=17)。地球化学特征显示:花岗岩属高钾钙碱性、弱过铝质花岗岩;样品的稀土元素组成以总体右倾,轻、重稀土分异明显和具明显的负铕异常为特征;微量元素具有富集 Rb、Th、U、La、Nd 等大离子亲石元素,亏损 Ba、Sr、Nb、P、Ti 等元素的特点。Sr Nd 同位素组成特征显示,花岗岩的源区可能是富集岩石圈地幔。初步研究认为,虎头崖矿床Ⅵ矿带花岗岩可能形成于中、晚三叠世碰撞后碰撞的构造背景下。  相似文献   
76.
孙伟  陈明  何江林  曹竣锋  王东 《沉积学报》2015,33(2):265-274
西藏羌塘盆地中生代发育广泛的海相碳酸盐地层,前人对该区地层的对比研究多局限于古生物地层学,本文尝试通过锶同位素地层学方法对上侏罗-下白垩统索瓦组地层进行全球对比。根据锶同位素地层学的基本原理,本文在对样品进行显微组构分析、阴极发光分析、Ca、Si、Sr和Mn等元素含量分析及评估其对同期海水代表性和样品溶解过程合理性的基础上,测试了羌塘盆地半岛湖地区上侏罗-下白垩统锶同位素组成,并建立了相应的演化曲线,进行了全球对比研究。结果表明,样品的锶同位素组成与前人已公布的同期海水锶同位素组成数据较为接近,其演化曲线与国际上已公布的锶同位素演化曲线有着较好的可对比性,晚侏罗-早白垩世时期全球海平面的变化和侵蚀作用的强弱是控制锶同位素演化曲线的主要因素。此外,通过对索瓦组海相碳酸盐锶同位素的研究,我们认为索瓦组的顶部可能延伸到早白垩世欧特里夫期,近而说明了羌塘盆地在早白垩世欧特里夫期还存在大规模的海相地层。  相似文献   
77.
西秦岭温泉斑岩钼矿床岩浆-热液演化   总被引:5,自引:3,他引:2  
邱昆峰  宋开瑞  宋耀辉 《岩石学报》2015,31(11):3391-3404
西秦岭北缘广泛出露印支期中酸性侵入岩和相关的斑岩-矽卡岩矿床。温泉矿床位于该矿带东段,是其内已探明规模最大的斑岩钼矿床。温泉矿床发育多阶段热液脉体,黄铁矿作为其中的贯通性金属硫化物,其化学组成蕴含着岩浆-热液演化及金属沉淀过程等诸多信息,对于斑岩系统模型的厘定具有重要意义。温泉矿床热液脉体时序为:钾长石-黑云母-石英脉(A脉)、石英-黄铜矿脉、石英-辉钼矿脉(B脉)和石英-绢云母-黄铁矿脉(D脉)。A脉是斑岩系统岩浆-热液演化的最早期脉体,主要矿物组合为钾长石+黑云母+石英+黄铁矿±磁铁矿±磷灰石±黄铜矿,代表了引起早期基性岩浆矿物被蚀变为黑云母的流体通道;B脉与钾长石化蚀变关系密切,围岩中斜长石斑晶大量被蚀变为钾长石;石英-辉钼矿脉切割所有早期黑云母化-钾化蚀变阶段的石英-硫化物网脉,并形成于所有斑岩侵位之后,少量黄铁矿和黄铜矿共生于辉钼矿裂隙及边部;D脉是斑岩系统岩浆-热液成矿作用的最晚期事件,其主要被黄铁矿和石英及少量黄铜矿填充,发育晚期的绢英岩化和泥化蚀变,长石多发生破坏性蚀变。四个阶段石英网脉中黄铁矿电子探针分析显示,A脉的黄铁矿中Cu、Mo和Au含量均较低,有少量的金属硫化物(黄铁矿+黄铜矿)沉淀,但通常不能形成规模矿体;石英-黄铜矿脉的黄铁矿中Cu含量明显较高,且多与高品位Cu矿体的空间产出位置相一致,可能是斑岩系统伴随钾化蚀变作用主要的铜沉淀阶段;B脉的黄铁矿中Mo含量明显较高,与高品位钼矿体空间产出关系密切,可能代表了斑岩系统钼成矿作用的主要阶段;D脉的黄铁矿中Au含量明显升高,可能代表了金在斑岩系统岩浆-热液成矿作用的最晚期事件中的沉淀。  相似文献   
78.
拜仁达坝-维拉斯托矿床是大兴安岭南段西坡最大的2个热液脉型银矿床, 对这两个矿床各阶段矿物(如黑钨矿、浅色闪锌矿、石英和萤石)中的流体包裹体进行研究, 并对硫化物进行了硫同位素分析.结果表明, 拜仁达坝矿床的流体从早阶段到晚阶段(Ⅰ→Ⅱ→Ⅲ)均一温度和盐度逐渐降低.维拉斯托矿床热液成矿期第Ⅰ、Ⅱ成矿阶段具有高温高盐度的流体; 第Ⅲ成矿阶段具有不混溶流体, 即中温中盐度的流体(均一温度为208~294 ℃, 盐度含量为4.65%~12.39%)和高温低盐度的流体(均一温度为333~406 ℃, 盐度含量为3.55%~6.88%); 第Ⅳ成矿阶段具有低温较低盐度的流体.两个矿床的流体包裹体气相成分表明成矿流体均为CO2-H2O-NaCl体系.拜仁达坝矿床的均一温度和盐度随着成矿阶段逐渐降低和氢氧同位素证据均表明, 早阶段的流体主要为岩浆水来源, 晚阶段的流体混入了大气降水.维拉斯托矿床氢氧同位素证据和流体中的成分(CH4/C2H6为39.271%~101.438%)均表明其成矿流体主要为岩浆水来源.拜仁达坝-维拉斯托矿床的硫具有深源特征, 拜仁达坝矿床的成矿机制主要与不同来源的成矿流体混合有关; 维拉斯托矿床的成矿机制主要与降温和成矿流体不混溶有关.   相似文献   
79.
本文对2012年秋季中国东海31个站位的海水样品中溶解态氨基酸(THAA)和颗粒态氨基酸(PAA)的分布与组成进行了研究。结果表明:表层海水中溶解游离氨基酸(DFAA)的平均浓度为0.12±0.04 μmol/L (0.06~0.19 μmol/L),溶解结合氨基酸(DCAA)的平均浓度为0.61±0.51 μmol/L (0.15~1.79 μmol/L),PAA的平均浓度为0.11±0.06 μmol/L (0.02~0.27 μmol/L)。THAA的水平分布特点大致为近岸高、远岸低;PAA的水平分布特点是近岸海域向远海海域分布呈现逐渐减小的趋势。THAA的垂直分布特点是由表层向底层逐渐降低。DCAA、PAA与Chl-a有很好的相关性,而DFAA与Chl-a的相关性不明显。东海表层海水中THAA的主要组分是天门冬氨酸、谷氨酸、丝氨酸、甘氨酸、苏氨酸及丙氨酸,PAA的主要组分是天门冬氨酸、谷氨酸、丝氨酸、甘氨酸、丙氨酸及亮氨酸。在表层海水中氨基酸是作为一个整体而对海洋生物地球化学过程产生影响的。  相似文献   
80.
This study investigates the benthic microbial responses to organic matter (OM) variations in quantity and sources in two shallow water bays (Fortaleza and Ubatuba Bays) on the SE coast of Brazil on six occasions during the year. The pelagic and benthic compartments of the bays were evaluated by: (i) nutrients and chlorophyll a (Chl a) in the water column; (ii) quantity and sources of OM in the sediment (Chl a, total organic carbon and total nitrogen and lipid biomarker composition); and (iii) microbial biomass in sediments as an indicator of active benthic response. Although there were changes in water‐column nutrients during the year, Chl a was fairly constant, suggesting a regular supply of microalgae‐derived OM to the sea bottom. Based on the composition of lipid biomarkers in sediments, OM sources were classified as mostly marine and with high contributions of labile (microalgae‐derived) OM. Labile OM composition varied from diatoms in the summer to phytoflagellates in the winter and tended to accumulate in areas protected by physical disturbances in one of the bays. Microbial biomass followed this trend and was 160% higher in protected than in exposed areas. This study suggests that the coupling between labile OM and benthic microbial biomass occurs primarily in protected areas, irrespective of the time of the year. Since meio‐ and macrofaunal assemblages depend upon secondary microbial production within the sediments, this coupling may have an important role for the benthic food‐web.  相似文献   
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