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931.
地球内部元素的配分行为具有重要意义,有助于揭示地球内部物质循环、元素成矿、超临界流体性质等基础地质问题。同步辐射微聚焦X射线荧光光谱(SR-μXRF)结合金刚石压腔(DAC)技术,可以在高温高压条件下实现高准确度和高分辨率的原位(in situ)测试元素在不同物相间的浓度,并获取配分系数。而基于地球化学热力学的理论计算模拟,可以获得元素在不同物相间的赋存形式,有助于揭示元素配分机制。本文综述了SR-μXRF结合DAC技术和地球化学热力学计算模拟原位测定高温高压下元素配分的研究方法,及其在地球内部元素迁移、成矿作用和地球早期形成过程等领域中的应用进展,认为利用该套方法研究高温高压下元素配分行为的体系将变得更加复杂,对温度、压力条件则要求更高。本文旨在更新和丰富高温高压下元素配分系数数据,深化对地球内部物质循环等问题的认知。 相似文献
932.
The goal of this study is to explain the origin of 234U–238U fractionation in groundwater from sedimentary aquifers of the St. Lawrence Lowlands (Quebec, Canada), and its relationship with 3He/4He ratios, to gain insight regarding the evolution of groundwater in the region. (234U/238U) activity ratios, or (234U/238U)act, were measured in 23 groundwater samples from shallow Quaternary unconsolidated sediments and from the deeper fractured regional aquifer of the Becancour River watershed. The lowest (234U/238U)act, 1.14 ± 0.01, was measured in Ca–HCO3-type freshwater from the Quaternary Shallower Aquifer, where bulk dissolution of the carbonate allows U to migrate into water with little 234U–238U isotopic fractionation. The (234U/238U)act increases to 6.07 ± 0.14 in Na–HCO3–Cl-type groundwater. Preferential migration of 234U into water by α-recoil is the underlying process responsible for this isotopic fractionation. An inverse relationship between (234U/238U)act and 3He/4He ratios has been observed. This relationship reflects the mixing of newly recharged water, with (234U/238U)act close to the secular equilibrium and containing atmospheric/tritiogenic helium, and mildly-mineralized older water (14C ages of 6.6 kyrs), with (234U/238U)act of ≥6.07 and large amounts of radiogenic 4He, in excess of the steady-state amount produced in situ. The simultaneous fractionation of (234U/238U)act and the addition of excess 4He could be locally controlled by stress-induced rock fracturing. This process increases the surface area of the aquifer matrix exposed to pore water, from which produced 4He and 234U can be released by α-recoil and diffusion. This process would also facilitate the release of radiogenic helium at rates greater than those supported by steady-state U–Th production in the rock. Consequently, sources internal to the aquifers could cause the radiogenic 4He excesses measured in groundwater. 相似文献
933.
The Wabigoon River (Ontario, Canada) was affected by dams starting in 1898 and was polluted with pulp and paper mill wastes starting in 1913 and mercury from a chlor-alkali plant from 1962 to 1975. A dated sediment core from a riverine lake was analysed to investigate resultant changes in the biogeochemistry of mercury as revealed by variations in mercury isotope ratios and sediment chemistry. A total mercury maximum formed by the mercury pollution coincided with minimums in the δ-values of the 198Hg/202Hg, 199Hg/202Hg, 200Hg/202Hg, and 201Hg/202Hg ratios, and the δ-values decreased in the order δ201Hg > δ200Hg > δ199Hg > δ198Hg. Thus, mass-dependent fractionation caused depletion in lighter isotopes, implying evaporation of Hg(0) and pollution of the atmosphere as well as the river-lake system. Concurrently, mass-independent fractionation caused 199Hg enrichment, possibly reflecting an independently documented upsurge in methylmercury production, and 201Hg depletion, suggesting removal of methylmercury with anomalously high 201Hg/199Hg ratios by aquatic organisms and accumulation of 201Hg-depleted inorganic Hg(II) in sediments. The δ201Hg/δ199Hg ratio rose abruptly when mercury pollution began, reflecting the resultant increase in methylmercury production, and remained high but gradually declined as the pollution abated, paralleling trends shown by methylmercury in aquatic organisms. The δ201Hg/δ199Hg ratio of pre-1962 background mercury increased ca. 1898 and ca. 1913–1929, suggesting accelerated methylmercury production due to stimulation of microbial activities by the damming of the river and the input of pulp and paper mill wastes, respectively. Other variations were linked to economic and technological factors that affected pulp and paper manufacture. 相似文献
934.
黔中茶店桥地下河流域不同水体硫酸盐浓度特征及来源识别 总被引:8,自引:0,他引:8
茶店桥地下河位于西南岩溶区,流域内"三水"转换迅速,地下水是当地的重要饮用水源。本文对流域内雨水、地表水、地下水中的SO_4~(2-)浓度进行了测试,利用氘(δD_(H_2O))、氧(δ~(18) O_(H_2O))同位素示踪地表水、地下水补给来源,用硫酸盐硫(δ~(34)S_(SO4))、氧(δ~(18) O_(SO4))同位素探讨了地表水、地下水中SO_4~(2-)的来源,并计算了地下河出口河水中不同SO_4~(2-)来源的贡献比例。结果表明:1不同水体中SO_4~(2-)浓度大小顺序为地表水地下水雨水,与邻近区域相比,茶店桥地下河流域雨水、地表水、地下水呈现富集SO_4~(2-)的特征。2地表水、地下水的主要补给来源为大气降水,硫酸不仅和HCO_3~-共同参与了流域内碳酸盐岩的溶解,也参与了雨水中含钙镁颗粒物的溶解。3地表水δ~(34)S_(SO4)、δ~(18) O_(SO4)值分别介于-12.98‰~-10.19‰和-0.54‰~+9.13‰之间,地下水δ~(34)S_(SO4)、δ~(18) O_(SO4)值分别介于-14.32‰~+16.58‰和+2.81‰~+14.35‰之间,SW02的SO_4~(2-)主要来源于大气降水,SW01、SW03、GW02、GW03、GW06主要来源于煤层,GW05主要来源于石膏,GW01、GW04为混合输入源。4地下河出口河水中大气降水带来的SO_4~(2-)贡献比例为13%,煤层硫化物氧化的贡献比例为40%,石膏溶解的贡献比例为47%。 相似文献
935.
纳米比亚欢乐谷地区白岗岩型铀矿成矿物质来源分析 总被引:3,自引:0,他引:3
本文对纳米比亚欢乐谷地区与铀成矿关系密切的白岗岩进行了系统的主量元素、微量元素及Sr-Nd同位素研究。结果表明,矿化白岗岩具有较高的SiO_2(68.81%~76.02%,平均值73.11%),富钾,A/CNK为0.96~1.07,平均值1.01,为亚碱性系列的准铝质-弱过铝质岩石。岩石富集轻稀土[LREE/HREE=2.53~7.71;(La/Yb)_N=2.14~10.40],Eu亏损中等,高Rb/Sr比值(2.03~5.50,平均值4.36),岩石同时富集Rb、Th、U、K及Pb等大离子亲石元素,亏损Ba、Nb、Ta及Sr等元素。岩石的初始~(87)Sr/~(86)Sr比值为0.73035~0.79345,ε_(Nd)(t)值为-13.5~-17.4,晶质铀矿的ε_(Nd)(t)值为-14.8~-16.5,两阶段Nd模式年龄为2.43~2.56Ga。元素和Sr-Nd同位素地球化学特征表明矿化白岗岩是在碰撞后的伸展构造环境中形成的,主成矿期的成矿物质来源于富铀的前达马拉基底;热液叠加改造期的铀可能来源于原生铀矿物本身。 相似文献
936.
Secondary Ion Mass Spectrometry Bias on Isotope Ratios in Dolomite–Ankerite,Part II: δ13C Matrix Effects 下载免费PDF全文
Maciej G. Śliwiński Kouki Kitajima Reinhard Kozdon Michael J. Spicuzza John H. Fournelle Adam Denny John W. Valley 《Geostandards and Geoanalytical Research》2016,40(2):173-184
This study is Part II of a series that documents the development of a suite of calibration reference materials for in situ SIMS analysis of stable isotope ratios in Ca‐Mg‐Fe carbonates. Part I explored the effects of Fe2+ substitution on SIMS δ18O bias measured from the dolomite–ankerite solid solution series [CaMg(CO3)2–CaFe(CO3)2], whereas this complementary work explores the compositional dependence of SIMS δ13C bias (calibrated range: Fe# = 0.004–0.789, where Fe# = molar Fe/(Mg+Fe)). Under routine operating conditions for carbonate δ13C analysis at WiscSIMS (CAMECA IMS 1280), the magnitude of instrumental bias increased exponentially by 2.5–5.5‰ (session‐specific) with increasing Fe‐content in the dolomite structure, but appeared insensitive to minor Mn substitution [< 2.6 mole % Mn/(Ca+Mg+Fe+Mn)]. The compositional dependence of bias (i.e., the matrix effect) was expressed using the Hill equation, yielding calibration residual values ≤ 0.3‰ relative to CRM NBS‐19 for eleven carbonate reference materials (6‐μm‐diameter spot size measurements). Based on the spot‐to‐spot repeatability of a drift monitor material that ‘bracketed’ each set of ten sample‐spot analyses, the analytical precision was ± 0.6–1.2‰ (2s, standard deviations). The analytical uncertainty for individual sample analyses was approximated by combining the precision and calibration residual values (propagated in quadrature), suggesting an uncertainty of ± 1.0–1.5‰ (2s). 相似文献
937.
Calcium Isotopic Fractionation during Ion‐Exchange Column Chemistry and Thermal Ionisation Mass Spectrometry (TIMS) Determination 下载免费PDF全文
Hong L. Zhu Zhao F. Zhang Gui Q. Wang Yu F. Liu Fang Liu Xin Li Wei D. Sun 《Geostandards and Geoanalytical Research》2016,40(2):185-194
Significant isotopic fractionation can occur during column chemistry and determination by mass spectrometry. Improper correction may produce uncertainties in the isotopic composition of geological samples. We investigated calcium isotopic fractionation during these two processes and set up a model to check data quality. The δ44/40Ca915a value of IAPSO seawater in different Ca cuts (e.g., 0–20, 20–40, 40–60, 60–80 and 80–100%) on column chemistry ranged from ~ 4‰ to 0‰. The more Ca was eluted, the lower the δ44/40Ca915a value of the elution was found. The isotopic fractionation of calcium on the column appeared to follow the exponential law. However, TIMS instrumental fractionation during Ca runs did not always follow the exponential law due to mixing effects from sample reservoirs on the filament. Our results show that errors could be caused if the instrumental fractionation deviates from the exponential law, especially when the fractionation degree is large. To improve the measurement uncertainty, a model is proposed to check the behaviour and degree of instrumental fractionation, which will provide a quick and reasonable verdict on the data quality of TIMS runs. 相似文献
938.
湖南七宝山铜多金属矿床石英斑岩时代与成因:锆石U-Pb定年及Hf同位素与稀土元素证据 总被引:1,自引:0,他引:1
湖南浏阳七宝山铜多金属矿床位于钦杭成矿带西段,是湘东北规模最大的铜多金属矿床。矿床的形成与区内的石英斑岩关系密切。石英斑岩内锆石具有岩浆锆石特征,LA-ICP-MS锆石U-Pb定年结果为155~153 Ma,代表其形成年龄,属晚侏罗世岩浆活动产物。岩浆锆石的~(176)Hf/~(177)Hf=0.282296~0.282603,εHf(t)=–12~–2.7,平均地壳模式年龄tDM2=1377~2056 Ma;锆石ΣREE=496~4162μg/g,(Yb/Nd)N=71.9~3133.8,HREE强烈富集,具有强烈Ce正异常(δCe=1.68~203.13)和强烈至中等Eu负异常(δEu=0.05~0.67),表明石英斑岩的岩浆源区具有明显壳源特征,来自于古元古代至中元古代地壳的部分熔融。结合岩石学研究,七宝山矿区石英斑岩的形成除了中下地壳冷家溪群或更古老的基底物质的部分熔融外,还有幔源组分加入,这一期岩浆与成矿作用与岩石圈拆离和软流圈物质上涌及随后的玄武岩底侵作用有关。 相似文献
939.
The food sources of aquacultured Apostichopus japonicus and the trophic levels of organisms in a sea cucumber(A. japonicus) and prawn(Penaeus japonica) polyculture system in a saltwater pond in Zhuanghe, Liaoning Province were examined using carbon and nitrogen stable isotopes. Across organisms, δ13C ranged from(–25.47±0.20)‰ to(–16.48±0.17)‰(mean±SD), and δ15N ranged from(4.23±0.49)‰ to(12.44±0.09)‰. The δ13C and δ15N contents of A. japonicus, P. japonica and Fenneropenaeus chinensis were comparatively higher than those of other organisms. Values of δ13C and δ15N revealed that P. japonica, Hemigrapsus sanguineus and Neomysis japonica comprised the largest component of the diet of A. japonicus. The mean trophic level of the organisms in this saltwater pond polyculture system was(2.75±0.08). P. japonica, A. japonicus, F. chinensis,Synechogobius hasta and Neomysis japonica were in the 3rd trophic level(2–3); jellyfish, H. sanguineus and zooplankton were in the 2nd trophic level(1–2); and Enteromorpha prolifera, benthic microalgae, periphyton and suspended matter primarily consisting of phytoplankton, bacteria and humus were in the primary trophic level(0–1). 相似文献
940.
扬子北缘马元铅锌矿床闪锌矿微量元素及S-Pb-He-Ar-C同位素地球化学研究 总被引:7,自引:3,他引:4
马元铅锌矿床是近年扬子陆块北缘铅锌找矿的新突破。矿体呈层状、似层状产于碑坝隆起翼部震旦系灯影组角砾状白云岩层间构造带中,围岩蚀变很弱。矿石中硫化物以闪锌矿、方铅矿为主,中粗粒晶质结构,充填于白云岩角砾间。闪锌矿富集Cd、Ge、Ag,贫In、Tl、Se,Ga/In为6~132,Ge/In多1000,成矿温度以中-低温为主。金属硫化物ε~(34)S值相对集中,为12.9‰~19.4‰,平均为17.4‰,来自于海相硫酸盐的还原。铅同位素组成稳定,~(206)Pb/~(204)Pb为17.858~17.918:~(207)Pb/~(204)Pb为15.603~15.694;~(208)Pb/~(204)Pb为37.756~38.046,具有造山带和上地壳铅的特征,震旦系可能提供了金属成矿物质。闪锌矿中流体包裹体的~3He/~4He为0.03Ra~1.05Ra,~(40)Ar/~(36)Ar为326.1~765.1,~(38)Ar/~(36)Ar为0.183~0.204,表明成矿流体主要为地壳流体和饱和大气水(大气降水或海水)的混合。闪锌矿内流体包裹体挥发分δ~(13)C_(CH_4)值为-36.01‰~-28.80‰,δ~(13)C_(C_2H_6)值为-27.72‰~-22.44‰,δ~(13)C_(CO_2)值为-23.24‰~-9.68‰,表明有机流体参与了成矿作用。石英、方解石的H-O同位素结果表明具有海水和有机水混合的特征。可见,成矿流体具有两种流体混合的特征,一为蒸发海水与围岩反应所形成的盆地卤水,二为有机流体。推测矿区可能存在一个古油气藏,由于TSR生成一高硫气藏,为区内还原性有机流体的主要来源。当富含Pb、Zn等成矿物质的成矿流体运移至富含CH_4和H_2S的还原性流体的矿区角砾岩带时,两种流体混合,Pb、Zn等遇到H_2S发生反应而沉淀成矿,并伴生热液白云石等,形成了马元铅锌矿床。综上所述,我们认为马元矿床属MVT型铅锌矿床。 相似文献