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61.
Major and trace element concentrations, as well as Sr and U isotope ratios, were measured in rainwater samples collected in three different locations in Alsace (East of France) and Luxembourg: a mid-altitude mountain site (Aubure Environment HydroGeochemical Observatory), an urban site (Strasbourg) and a peri-urban site located in an area of well developed industrial activity (Esch-sur-Alzette in Luxembourg). Results highlight the quite high spatial and temporal variability of the chemical and isotopic characteristics of rainwater at the regional scale. They also suggest a quite systematic contribution of a local component in the chemical composition of rainwater. In urban and peri-urban sites, the local component is certainly linked to human activities, as it is well illustrated in this study with the Esch-sur-Alzette samples. On the other hand, for the Aubure site, i.e. a small forested watershed of mid-altitude mountain, data presented in this study demonstrate the influence of the vegetation on the chemical composition of rainwater for alkali and calc-alkali elements, as well as for the Sr isotope ratios. Such a result questions the reliability of the method classically used to estimate the rainwater contribution on the river chemical budget. In addition, data of the present study confirm the very low content of uranium in rainwater and demonstrate, especially through the U isotope analysis of Aubure rainwater, the negligible effect of rainwater on U budget of river waters. This work thus outlines the property of U to be a geochemical tracer specific of weathering fluxes carried by rivers. To cite this article: F. Chabaux et al., C. R. Geoscience 337 (2005).  相似文献   
62.
Zircon, monazite and xenotime crystallized over a temperature interval of several hundred degrees at the magmatic to hydrothermal transition of the Sn and W mineralized Mole Granite. Magmatic zircon and monazite, thought to have crystallized from hydrous silicate melt, were dated by conventional U–Pb techniques at an age of 247.6 ± 0.4 and 247.7 ± 0.5 Ma, respectively. Xenotime occurring in hydrothermal quartz is found to be significantly younger at 246.2 ± 0.5 Ma and is interpreted to represent hydrothermal growth. From associated fluid inclusions it is concluded that it precipitated from a hydrothermal brine ≤ 600 °C, which is below the accepted closure temperature for U–Pb in this mineral. These data are compatible with a two-stage crystallization process: precipitation of zircon and monazite as magmatic liquidus phases in deep crustal magma followed by complete crystallization and intimately associated Sn–W mineralization after intrusion of the shallow, sill-like body of the Mole Granite. Later hydrothermal formation of monazite in a biotite–fluorite–topaz reaction rim around a mineralized vein was dated at 244.4 ± 1.4 Ma, which distinctly postdates the Mole Granite and is possibly related to a younger hidden intrusion and its hydrothermal fluid system.

Obtaining precise age data for magmatic and hydrothermal minerals of the Mole Granite is hampered by uncertainties introduced by different corrections required for multiple highly radiogenic minerals crystallising from evolved hydrous granites, including 230Th disequilibrium due to Th/U fractionation during monazite and possibly xenotime crystallization, variable Th/U ratios of the fluids from which xenotime was precipitating, elevated contents of common lead, and post-crystallization lead loss in zircon, enhanced by the fluid-saturated environment. The data imply that monazite can also survive as a liquidus phase in protracted magmatic systems over periods of 106 years. The outlined model is in agreement with prominent chemical core-rim variation of the zircon.  相似文献   

63.
Robert L. Linnen   《Lithos》2005,80(1-4):267-280
The solubilities of columbite, tantalite, wolframite, rutile, zircon and hafnon were determined as a function of the water contents in peralkaline and subaluminous granite melts. All experiments were conducted at 1035 °C and 2 kbar and the water contents of the melts ranged from nominally dry to approximately 6 wt.% H2O. Accessory phase solubilities are not affected by the water content of the peralkaline melt. By contrast, solubilities are affected by the water content of the subaluminous melt, where the solubilities of all the accessory phases examined increase with the water content of the melt, up to 2 wt.% H2O. At higher water contents, solubilities are nearly constant. It can be concluded that water is not an important control of accessory phase solubility, although the water content will affect diffusivities of components in the melt, thus whether or not accessory phases will be present as restite material. The solubility behaviour in the subaluminous and peralkaline melts supports previous spectroscopic studies, which have observed differences in the coordination of high field strength elements in dry vs. wet subaluminous granitic glasses, but not for peralkaline granitic glasses. Lastly, the fact that wolframite solubility increases with increasing water content in the subaluminous melt suggests that tungsten dissolved as a hexavalent species.  相似文献   
64.
Yudai is a newly discovered copper deposit associated with a porphyritic quartz diorite, in the Kalatag district of the eastern Tianshan, China. SHRIMP U-Pb dating of zircons from the diorite yielded an age of 432 ± 3 Ma. The diorite is peraluminous (ASI = 0.98–1.10), calc-alkaline to tholeiitic with high Al2O3 of 16.6–17.7 wt% and Mg# of 57.4–67.4. Trace element characteristics of the diorite show it is enriched in Ba, K and Sr, and depleted in Nb, Ta, Ti, with a positive Eu anomaly and high Sr/Y and La/Yb ratios. This diorite has positive εNd(t) values ranging from 6.2 to 8.4 with low initial 87Sr/86Sr ratios of 0.704336 to 0.704450. These geochemical and isotopic characteristics indicate that the adakite-like diorite, associated with the copper mineralization, was emplaced in an island arc setting and resulted from partial melting of subducted oceanic plate in a mantle wedge.  相似文献   
65.
The growth and dissolution behaviour of accessory phases (and especially those of geochronological interest) in metamorphosed pelites depends on, among others, the bulk composition, the prograde metamorphic evolution and the cooling path. Monazite and zircon are arguably the most commonly used geochronometers for dating felsic metamorphic rocks, yet crystal growth mechanisms as a function of rock composition, pressure and temperature are still incompletely understood. Ages of different growth zones in zircon and monazite in a garnet‐bearing anatectic metapelite from the Greater Himalayan Sequence in NW Bhutan were investigated via a combination of thermodynamic modelling, microtextural data and interpretation of trace‐element chemical ‘fingerprint’ indicators in order to link them to the metamorphic stage at which they crystallized. Differences in the trace‐element composition (HREE, Y, EuN/Eu*N) of different phases were used to track the growth/dissolution of major (e.g. plagioclase, garnet) and accessory phases (e.g. monazite, zircon, xenotime, allanite). Taken together, these data constrain multiple pressure–temperature–time (P–T–t) points from low temperature (<550 °C) to upper amphibolite facies (partial melting, >700 °C) conditions. The results suggest that the metapelite experienced a cryptic early metamorphic stage at c. 38 Ma at <550 °C, ≥0.85 GPa during which plagioclase was probably absent. This was followed by a prolonged high‐T, medium‐pressure (~600 °C, 0.55 GPa) evolution at 35–29 Ma during which the garnet grew, and subsequent partial melting at >690 °C and >18 Ma. Our data confirm that both geochronometers can crystallize independently at different times along the same P–T path and that neither monazite nor zircon necessarily provides timing constraints on ‘peak’ metamorphism. Therefore, collecting monazite and zircon ages as well as major and trace‐element data from major and accessory phases in the same sample is essential for reconstructing the most coherent metamorphic P–T–t evolution and thus for robustly constraining the rates and timescales of metamorphic cycles.  相似文献   
66.
A sequence of shallow reef cores from Heron Reef, Great Barrier Reef, provides new insights into Holocene reef growth models. Isochron analysis of a leeward core transect suggests that the north‐western end of Heron Reef reached current sea‐level by ca 6·5 kyr bp and then prograded leeward at a rate of ca 19·6 m/kyr between 5·1 kyr and 4·1 kyr bp (pre‐1950) to the present reef margin. A single short core on the opposing margin of the reef is consistent with greater and more recent progradation there. Further to the east, one windward core reached modern sea‐level by ca 6·3 kyr bp , suggesting near ‘keep‐up’ behaviour at that location, but the opposing leeward margin behind the lagoon reached sea‐level much more recently. Hence, Heron Reef exhibited significantly different reef growth behaviour on different parts of the same margin. Mean reef accretion rates calculated from within 20 m of one another in the leeward core transect varied between ca 2·9 m and 4·7 m/kyr depending on relative position in the prograding wedge. These cores serve as a warning regarding the use of isolated cores to inform reef growth rates because apparent aggradation at any given location on a reef varies depending on its location relative to a prograding margin. Only transects of closely spaced cores can document reef behaviour adequately so as to inform reef growth models and sea‐level curves. The cores also emphasize potential problems in U‐series dates for corals within a shallow (ca 1·5 m) zone beneath the reef flat. Apparent age inversions restricted to that active diagenetic zone may reflect remobilization and concentration of Th in irregularly distributed microbialites or biofilms that were missed during sample vetting. Importantly, the Th‐containing contaminant causes ages to appear too old, rather than too young, as would be expected from younger cement.  相似文献   
67.
在乌拉特后旗—达茂旗—四子王旗一带的内蒙古中部地区分布着超基性-酸性连续岩浆系列,开展其岩体年代学、地球化学研究可为内蒙古中部地区与超基性-基性岩有关的铜镍矿成矿规律研究提供基础地质资料,还可以推断岩浆侵位时期的区域大地构造背景。本文以达茂旗黄花滩铜镍矿区出露的辉长岩为研究对象,采用LA-ICP-MS仪器对无裂隙、高透明度、阴极发光均匀、环带清晰的锆石进行U-Pb定年,获得岩体加权平均年龄为262.4±1.1 Ma,并利用XRF和ICP-MS进行岩石地球化学分析显示黄花滩辉长岩具有后碰撞拉伸环境下的岩浆特征。综合前人相关研究认为,内蒙古中部地区于中二叠世晚期(255~275 Ma)已经进入后碰撞构造阶段,而古亚洲洋在该区域的闭合应发生在晚二叠世前(~285 Ma),此结论丰富了古亚洲洋闭合时间上限及中晚二叠世期间内蒙古中部地区构造背景方面的证据。  相似文献   
68.
王军  万传辉  赖湘濡  杨坤光 《地质论评》2016,62(S1):335-336
粤北下庄矿田是我国南方重要的花岗岩型铀矿产地,矿田内部基性岩脉与铀矿成矿具有密切关系,侵位于产铀岩体-下庄岩体。野外地质接触关系表明,下庄岩体侵位较早,晚期NNE向岩脉在下庄岩体内部侵位,两者呈侵入接触关系。通过对太平庵地区岩脉的野外地质特征和岩石薄片镜下特征,认为岩脉多具杏仁构造,为斑状结构,斑晶主要为角闪石和斜长石,定名为闪长玢岩。本次研究团队通过锆石U-Pb年代学测试表明下庄岩体侵位时间为245Ma,矿田内部近EW向分布的五组辉绿岩脉侵位时间为193±4Ma(王连训等,2011),本人结合NNE向岩脉的锆石CL图像、U-Pb年龄分析了岩脉的年代学特征,认为样品的206Pb/238U年龄介于231~253 Ma之间(MSWD=0.77),加权平均结果为242±2Ma (MSWD=8.9),代表了太平庵地区NNE向中性岩脉闪长玢岩的侵位结晶年龄。  相似文献   
69.
贵州西北部发育多处基性侵入岩,总体规模较小(约0.25 Km2),多沿深大断裂侵位,出露于铅锌矿点外围,本文对猫猫厂、凉山两处矿点附近的儿马冲和白岩庆两地小型基性侵入岩进行了重点研究。侵入岩主要岩性为细粒辉长岩,造岩矿物主要为拉长石、普通辉石。SiO2范围为49.60-51.09 wt%,MgO从3.88-4.27 wt %,TiO2为3.69-3.85 wt %。LA-ICP-MS锆石U-Pb定年结果为268.3±7.4 Ma,显示岩浆侵位于二叠纪。基性侵入岩的微量元素蛛网图呈OIB型特征,富集大离子亲石元素(LILE)、轻稀土元素(LREE),亏损重稀土元素(HFEE),相对亏损高场强元素(Nb,Ta),有Sr、Y亏损,Pb富集。(87Sr/86Sr)i范围0.706749~0.707069,(143Nd/144Nd)i范围0.512313~0.512363,εNd(t)范围0.2~1.2;源区熔融深度处于石榴石橄榄岩相深度,可能经历了1-3 %的部分熔融,处于亏损石榴石二辉橄榄岩相向原始石榴石二辉橄榄岩相的过渡区。成岩过程中发生了单斜辉石、斜长石等矿物分离结晶,受到了有限的地壳混染作用,未经历明显的AFC过程。地壳物质在地幔源区中的加入可能是造成地幔富集的主要原因。侵入岩与成矿作用之间的关系,主要通过两方面所表现。一方面是二者间构造活动上的耦合性。另一方面是基性岩在成矿过程中可能发挥了重要的化学屏障层作用。  相似文献   
70.
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   
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