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51.
LCT型伟晶岩及其锂矿床成因概述   总被引:2,自引:0,他引:2  
张辉  吕正航  唐勇 《地质学报》2021,95(10):2955-2970
花岗伟晶岩具有与低共熔花岗岩相似的矿物和化学组成,通常与高分异花岗岩具有成因联系.花岗伟晶岩划分为富Li-Cs-Ta (LCT)、富Nb-Y-F (NYF)和混合的LCT+NYF型,其中LCT型伟晶岩以过铝质,富集助熔组分(H2O、F、P、B)、稀有元素(Li、Rb、Cs、Nb、Ta、Be、Sn),极其低的Nb/Ta比值(<5)为特征.通常LCT型伟晶岩显示内部分带,主要包括边界带、壁带、中间带和核部带;此外,可能还发育交代体、层状细晶岩和晶洞.大多数LCT型伟晶岩形成与(同造山)-晚造山的过铝质S型、Ⅰ型或混合的S+Ⅰ型花岗岩具有成因联系.对于壳源沉积岩小比例部分熔融直接形成的伟晶岩,通常形成于伸展背景下的晚造山和造山后阶段,侵入于典型的低压角闪岩-高绿片岩相的变沉积岩中.伟晶岩外带(包括边缘带、壁带、细晶岩)中的细粒和细晶岩结构、UST(单向固结结构)是液相线过冷所致,而伟晶岩内带(中间带、核部带)中粗大矿物形成、矿物分带以及稀有金属矿物的饱和结晶是助熔组分(H2O、B、P、F)、稀有金属(Li、Rb、Cs、Be、Nb、Ta)通过组成带状纯化方式在边界层聚集的结果.伟晶岩分离结晶作用的开始与液相线过冷状态密切相关,晶体成核延迟、晶体生长速率、晶体成核密度取决于液相线过冷程度(ΔT).针对LCT型伟晶岩,已提出的稀有金属成矿机制主要有分离结晶作用、岩浆不混溶、超临界流体和组成带状纯化.对于全脉矿化锂辉石伟晶岩成因,尚不清楚是岩浆液态分离还是Li强烈分配进入流体相所致?  相似文献   
52.
综合地球化学、高分辨层序地层学理论方法,利用双河露头资料及样品分析测试,采用多元统计方法优选出陆源输入强度相关元素组合Al-K-Ti-Mg-Rb-Cr-Zr、自生沉淀强度相关元素组合Ca-Mn-Ba-Co、有机质吸附及还原强度相关元素组合V-Ni-Mo-U-Cu-Zn作为化学层序地层划分指标体系,将双河露头五峰组划分为LCW四级层序,龙马溪组下段自下而上细分为MCL1-1、MCL1-2、MCL1-3、MCL1-4四级层序。陆源输入强度相关主微量元素组合总量在层序界面附近相对较高,而最大海泛面附近相对较低,具有元素总量减少-增加旋回性变化特征;而自生沉淀强度相关主量元素组合总量和微量元素组合总量、有机质吸附及还原强度相关微量元素组合总量在层序界面附近一般较低,在最大海泛面附近一般较高,具元素总量增多-减少旋回性变化特征。  相似文献   
53.
王会敏 《地质与勘探》2023,59(6):1240-1249
鄂西黄陵背斜地区虽已发现众多矿点,但是矿床规模较小,找矿潜力不明。由于区内植被茂盛、覆盖严重,致使地质异常信息被削弱或掩盖,对进一步找矿工作造成了严重干扰。本次研究使用成分数据分析和能谱-面积(S-A)分形模型识别与金矿化相关的异常,结果表明:(1)等距对数比(ILR)变换后的主成分分析结果相比对数(Log)变换更能够反应元素的共生组合规律,第一主成分(PC1)元素组合为Au-Cu-Ag,且Au元素占有最大的载荷,与金矿密切相关,PC1元素组合异常的分布模式与矿点的分布更加吻合;(2) S-A方法抑制了黄陵背斜区域水系沉积物的背景模式,增强了异常模式;(3)根据地质特征和以往勘查工作情况,圈定了三处找矿远景区,为该地区金矿下一步勘查工作提供了重要依据。  相似文献   
54.
Simultaneous analysis of carbon and nitrogen isotope ratios by SIMS was applied for the first-time to a natural diamond from the Kelsey Lake kimberlite, State Line Distinct, Colorado (UWD-1). This in situ procedure is faster, reduces sample size for analysis, and measures both isotope ratios from a single ~ 10 μm diameter pit, a critical advantage for zoned diamonds. The carbon isotope ratio (expressed as δ13CVPDB) of the bulk UWD-1 crystal, determined by the conventional combustion method in the present study, is -5.9‰ ± 0.2‰ (VPDB, 2s). Nitrogen mass fraction ([N]) and isotope ratio (expressed as δ15NAir) were determined by stepwise combustion and gas-source mass-spectrometry, resulting in 553 ± 64 μg g-1 and -6.7‰ ± 1.1‰ (Air, 2s), respectively. Secondary ions of 12C2-, 12C13C-, 12C14N-, and 12C15N- were simultaneously measured by SIMS using three Faraday cups and one electron multiplier. The spot-to-spot reproducibility of δ13C and δ15N values for the UWD-1 (178 spots on sixteen chips, 10 μm spots), were 0.3‰ and 1.6‰, respectively (2s). While 12C14N-/12C2- ratios, which are an indicator for [N], varied up to 12% among these sixteen chips, such variation did not correlate with either δ13C or δ15N values. We propose that UWD-1 is a suitable reference sample for microscale in situ analysis of δ13C and δ15N values in diamond samples.  相似文献   
55.
针对月核大小及密度估计问题,利用高分辨率重力场模型GL1500E的二阶位系数和LLR(lunar laser ranging)天平动参数,考虑月核分层为外核和内核的情况,结合非线性粒子群优化算法,对月核大小和组成进行了估计。大批量的统计结果表明,大概率分布的外核半径rc1约为469 km,内核半径rc2约为303 km,外核密度ρc1约为4613 kg/m3,内核密度ρc2约为7004 kg/m3,月幔密度ρm约为3340 kg/m3。月幔密度非常接近地质研究结果3360 kg/m3,内外核半径与近期其他研究结果相近,估算的月核大小与密度组成具有一定的参考价值。若月核由纯铁和硫化亚铁组成,则研究表明,内核大部分由纯铁组成,外核大部分由硫化亚铁组成。  相似文献   
56.
文章根据2016年5月、8月、11月和2017年2月在防城河口湾海域进行的渔业资源和环境调查数据, 研究了河口湾鱼类群落结构及其空间和季节变化, 分析了鱼类群落结构与主要环境因子的关系。结果表明: 全年调查共渔获鱼类95种, 隶属于2纲12目37科69属, 适温性以暖水性鱼类为主, 生态类型以底层和近底层鱼类为主。其中, 春季60种, 夏季59种, 秋季54种, 冬季46种, 夏—秋季间种类相似性指数最高。全年优势种为褐菖鲉Sebastiscus marmoratus和长鳍篮子鱼Siganus canaliculatus, 主要种有黄鳍棘鲷Acanthopagrus latus、条马鲾Equulites rivulatus、李氏?Callionymus richardsoni和真赤鲷Pagrus major等10种; 夏、秋季的最大优势种均为长鳍篮子鱼, 春、冬季的最大优势种分别为褐菖鲉和条马鲾。全湾鱼类年均资源密度为45836尾·km -2和 435.21kg·km -2, 资源密度具有明显的空间差异和季节变化。全年各站位种数变化范围在2~21种, 多样性指数H′在0.468~4.031, 丰富度指数d在0.120~1.926, 均匀度指数J在0.181~0.969。聚类分析、单因子相似性分析(ANOSIM)及相似性百分比(SIMPER) 分析表明该海域鱼类群落存在一定程度的时空异质性。相关性分析表明影响防城河口湾鱼类群落结构的主要环境因子为水温、盐度和硝酸盐。  相似文献   
57.
Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO2 balance, it is important to identify the characteristics and driving factors of chemical weathering and CO2 consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO2, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km−2 yr−1, respectively, in maximum) and potential net release of CO2 (with an upper constraint of 35.6 and 35.2 t km−2 yr−1, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.  相似文献   
58.
Analyses (n = 525) of chloride (Cl), bromide (Br), nitrate as nitrogen (NO3-N), sodium (Na+), calcium (Ca2+) and potassium (K+) in stream water, tile-drain water and groundwater were conducted in an urban-agricultural watershed (10% urban/impervious, 87% agriculture) to explore potential differences in the signature of Cl originating from an urban source as compared with an agricultural source. Only during winter recharge events did measured Cl concentrations exceed the 230 mg/L chronic threshold. At base flow, nearly all surface water and tile water samples had Cl concentrations above the calculated background threshold of 18 mg/L. Mann–Whitney U tests revealed ratios of Cl to Br (p = .045), to NO3-N (p < .0001), to Ca2+ (p < .0001), and to Na+ (p < .0001) to be significantly different between urban and agricultural waters. While Cl ratios indicate that road salt was the dominant source of Cl in the watershed, potassium chloride fertilizer contributed as an important secondary source. Deicing in watersheds where urban land use is minimal had a profound impact on Cl dynamics; however, agricultural practices contributed Cl year-round, elevating stream base flow Cl concentrations above the background level.  相似文献   
59.
To better understand the mechanisms relating to hydrological regulations of chemical weathering processes and dissolved inorganic carbon (DIC) behaviours, high-frequency sampling campaigns and associated analyses were conducted in the Yu River, South China. Hydrological variability modifies the biogeochemical processes of dissolved solutes, so major ions display different behaviours in response to discharge change. Most ions become diluted with increasing discharge because of the shortened reactive time between rock and water under high-flow conditions. Carbonate weathering is the main source of major ions, which shows strong chemostatic behaviour in response to changes in discharge. Ions from silicate weathering exhibit a significant dilution effect relative to the carbonate-sourced ions. Under high temperatures, the increased soil CO2 influx from the mineralisation of organic material shifts the negative carbon isotope ratios of DIC (δ13CDIC) during the high-flow season. The δ13CDIC values show a higher sensitivity than DIC contents in response to various hydrological conditions. Results from a modified isotope-mixing model (IsoSource) demonstrate that biological carbon is a dominant source of DIC and plays an important role in temporal carbon dynamics. Furthermore, this study provides insights into chemical weathering processes and carbon dynamics, highlighting the significant influence of hydrological variability to aid understanding of the global carbon cycle.  相似文献   
60.
In the classical view of metamorphic microstructures, fast viscous relaxation (and so constant pressure) is assumed, with diffusion being the limiting factor in equilibration. This contribution is focused on the only other possible scenario – fast diffusion and slow viscous relaxation – and brings an alternative interpretation of microstructures typical of high‐grade metamorphic rocks. In contrast to the pressure vessel mechanical model applied to pressure variation associated with coesite inclusions in various host minerals, a multi‐anvil mechanical model is proposed in which strong single crystals and weak grain boundaries can maintain pressure variation at geological time‐scales in a polycrystalline material. In such a mechanical context, exsolution lamellae in feldspar are used to show that feldspar can sustain large differential stresses (>10 kbar) at geological time‐scales. Furthermore, it is argued that the existence of grain‐scale pressure gradients combined with diffusional equilibrium may explain chemical zoning preserved in reaction rims. Assuming zero net flux across the microstructure, an equilibrium thermodynamic method is introduced for inferring pressure variation corresponding to the chemical zoning. This new barometric method is applied to plagioclase rims around kyanite in felsic granulite (Bohemian Massif, Czech Republic), yielding a grain‐scale pressure variation of 8 kbar. In this approach, kinetic factors are not invoked to account for mineral composition zoning preserved in rocks metamorphosed at high grade.  相似文献   
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