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21.
准噶尔盆地是我国重要的多能源矿产产出盆地之一,而准噶尔盆地南缘头屯河地区也是我国砂岩型铀矿找矿的优选区段,为了厘定头屯河地区砂岩型铀矿赋矿层位沉积期的源区位置、母岩岩性及时代,本文在野外地质调查的基础上,对头屯河地区砂岩型铀矿赋矿层中的碎屑锆石进行了LA-ICP-MS U-Pb定年和Hf同位素分析,建立了碎屑锆石的U-Pb年龄及Hf模式年龄谱系。通过与周缘岩浆活动时代对比,并结合古流向数据进一步分析赋矿层位沉积期的源区位置及母岩岩性,讨论砂岩型铀矿的铀源条件。对采自侏罗系和下白垩统的4个砂岩样品进行碎屑锆石年龄分析表明:碎屑锆石U-Pb年龄存在140~180 Ma、240~320 Ma、340~420 Ma、440~480 Ma四个主峰值年龄段,年龄较平均的分布在210~480 Ma宽泛的区间内。研究表明头屯河地区早侏罗世物源来自北天山;中侏罗世物源来自中、南天山;中侏罗晚期开始转变为以北天山为主;早白垩世物源大部分来自中、北天山,少量来自博格达山地区。砂岩型铀矿化层铀源主要来自南侧天山地区的古生代中酸性火成岩,其成矿作用应该发生在盆地处于较稳定的构造环境中。  相似文献   
22.
王昆  李伟强  李石磊 《地学前缘》2020,27(3):104-122
钾稳定同位素是重要的非传统稳定同位素体系,也是近年来迅速发展的热门研究课题。对钾同位素研究历史和现状进行综述,具体包括以下内容:(1)总结了钾元素的地球化学和宇宙化学性质,包括钾在主要地质储库(地幔、地壳、海洋)中的丰度及其分配,钾在岩浆演化中的不相容大离子亲石性,常见含钾火成岩/沉积岩矿物以及钾在表生过程中的循环,也包括主要行星物质(球粒陨石、非球粒陨石、火星和灶神星陨石以及月球样品)中钾的含量、赋存状态、主要矿物,钾在太阳星云冷凝、行星积聚以及岩浆海过程中的中等挥发性质;(2)介绍了钾同位素的研究历史,从1922年Dempster利用最早的质谱仪测量钾同位素在自然界的丰度,到Taylor和Urey在1938发表的经典的钾同位素分馏实验,再到Humayun和Clayton在1995年发表的钾同位素领域的经典研究,最后到近几年的进展;(3)介绍了对钾的前处理(离子交换柱法)以及钾同位素的主要测量方法,包括早期热电离质谱仪法(TIMS),二次离子质谱仪法(SIMS)和近十几年以来高速发展的多接收电感耦合等离子体质谱仪法(MC-ICP-MS)及其不同的技术路线;(4)介绍了高精度钾同位素比值在低温地球化学和生物地球化学中的应用,包括钾同位素在地表的风化过程中、海水洋壳的反向风化作用中的分馏及其在示踪全球钾元素循环和洋壳俯冲等过程中的应用;(5)介绍了高精度钾同位素比值在高温地球化学中的应用,包括钾同位素在岩浆分异和矿物结晶过程中的分馏;(6)介绍了高精度钾同位素比值在宇宙化学中的应用,包括在太阳星云冷凝、行星凝聚、月球形成大碰撞、岩浆海、火山喷发去气过程中的分馏作用。  相似文献   
23.
为了探讨琼东南盆地华光凹陷海底天然气水合物稳定带的分布规律,定量研究了静水压力、底水温度、地温梯度和气源组分对水合物稳定带的影响程度。在此基础上,分析了华光凹陷现今甲烷水合物稳定带的厚度分布。最后,综合各因素的历史演化过程,初步探讨了华光凹陷1.05 Ma BP以来天然气水合物稳定带的演化。结果表明:(1)气源组分和海底温度的变化对研究区内水合物稳定带的影响较大;水合物稳定带厚度与海底温度呈良好的线性负相关性。(2)水深超过600 m的海域具备形成天然气水合物的温压条件;超过600 m水深的海域水合物稳定带厚度大部分超过 100 m,其中西北部稳定带的最大厚度超过300 m,是有利的水合物勘探区。(3)华光凹陷1.05 Ma BP以来天然气水合物稳定带厚度经历了快速增厚–窄幅变化–快速减薄和恢复的过程。麻坑群与水合物稳定变化敏感区在空间上具有较好的叠合关系。结合前人的研究成果,推测其形成与天然气水合物的分解释放有关。  相似文献   
24.
陈敏  曾健  杨伟锋 《海洋学报》2018,40(10):32-41
同位素在确定物质来源、指示生物地球化学循环路径、定量生物地球化学过程速率等方面具有独特的优势,本文以近海生态环境变化研究中常用的稳定同位素(13C、15N、18O)和放射性核素(14C、234Th、232Th、230Th、228Th、210Po、210Pb、137Cs、226Ra、228Ra、224Ra、223Ra)为对象,介绍它们在揭示海洋有机质来源、食物网结构、水体缺氧机制、氮循环过程、颗粒动力学、海底地下水输入、有机地球化学过程、沉积年代学等方面的应用,侧重于总结我国近海生态环境研究中同位素示踪取得的进展。伴随着我国经济的发展,近百年来我国近海生态环境也发生了明显的变化,基于同位素示踪揭示的近海富营养化和沉积环境的演变规律表明,我国近海生态环境自20世纪50年代起经历持续的变化,特别是在过去20~30年时间里,近海生态环境的变化尤为剧烈,反映出人类活动是我国近海生态环境变化的主要驱动力。未来需要通过发展新的同位素技术及拓展更广泛的应用,围绕近海海洋生态环境变化的突出问题,重点揭示近海生态环境变化的响应特征、变化速率和作用机制,从而系统地掌握近海生态环境的时空变化规律。  相似文献   
25.
Ressi is a small (2.4 ha) forested catchment located in the Italian pre-Alps. The site became an experimental catchment to investigate the water fluxes in the soil–plant–atmosphere continuum and the impact of vegetation on runoff generation in 2012. The elevation of the catchment ranges from 598 to 721 m a.s.l. and the climate is humid temperate. The bedrock consists of rhyolites and dacites; the soil is a Cambisol. The catchment is covered by a dense forest, dominated by beech, chestnut, maple, and hazel trees. The field set up includes measurements of the rainfall in an open area, streamflow at the outlet, soil moisture at various depths and locations, and depth to water table in six piezometers at a 5- or 10-min interval. Samples of precipitation, stream water, shallow groundwater and soil water are collected monthly for tracer analysis (stable isotopes (2H and 18O), electrical conductivity and major ions), and during selected rainfall–runoff events to determine the contribution of the various sources to runoff. Since 2017, soil and plant water samples have been collected to determine the sources of tree transpiration. Data collected in the period 2012–2016 are publicly available. Data collection is ongoing, and the data set is expected to be updated on an annual basis to include the most recent measurements.  相似文献   
26.
The direct H2Oliquid–H2Ovapour equilibration method utilizing laser spectroscopy (DVE-LS) is a way to measure soil pore water stable isotopes. Various equilibration times and calibration methods have been used in DVE-LS. Yet little is known about their effects on the accuracy of the obtained isotope values. The objective of this study was to evaluate how equilibration time and calibration methods affect the accuracy of DVE-LS. We did both spiking and field soil experiments. For the spiking experiment, we applied DVE-LS to four soils of different textures, each of which was subjected to five water contents and six equilibration times. For the field soil experiment, we applied three calibration methods for DVE-LS to two field soil profiles, and the results were compared with cryogenic vacuum distillation (CVD)-LS. Results showed that DVE-LS demonstrated higher δ2H and δ18O as equilibration time increased, but 12 to 24 hr could be used as optimal equilibration time. For field soil samples, DVE-LS with liquid waters as standards led to significantly higher δ2H and δ18O than CVD-LS, with root mean square error (RMSE) of 8.06‰ for δ2H and 0.98‰ for δ18O. Calibration with soil texture reduced RMSE to 3.53‰ and 0.72‰ for δ2H and δ18O, respectively. Further, calibration with both soil texture and water content decreased RMSE to 3.10‰ for δ2H and 0.73‰ for δ18O. Our findings conclude that the calibration method applied may affect the measured soil water isotope values from DVE-LS.  相似文献   
27.
Questions persist about interpreting isotope ratios of bound and mobile soil water pools, particularly relative to clay content and extraction conditions. Interactions between pools and resulting extracted water isotope composition are presumably related to soil texture, yet few studies have manipulated the bound pool to understand its influence on soil water processes. Using a series of drying and spiking experiments, we effectively labelled bound and mobile water pools in soils with varying clay content. Soils were first vacuum dried to remove residual water, which was then replaced with heavy isotope-enriched water prior to oven drying and spiking with heavy isotope-depleted water. Water was extracted via centrifugation or cryogenic vacuum distillation (at four temperatures) and analysed for oxygen and hydrogen isotope ratios via isotope ratio mass spectrometry. Water from centrifuged samples fell along a mixing line between the two added waters but was more enriched in heavy isotopes than the depleted label, demonstrating that despite oven drying, a residual pool remains and mixes with the mobile water. Soils with higher clay + silt content appeared to have a larger bound pool. Water from vacuum distillation samples have a significant temperature effect, with high temperature extractions yielding progressively more heavy isotope-enriched values, suggesting that Rayleigh fractionation occurred at low temperatures in the vacuum line. By distinctly labelling bound and mobile soil water pools, we detected interactions between the two that were dependent on soil texture. Although neither extraction method appeared to completely extract the combined bound and mobile (total water) pool, centrifugation and high temperature cryogenic vacuum distillations were comparable for both δ2H and δ18O of soil water isotope ratios.  相似文献   
28.
In 1994, a network of small catchments (GEOMON) was established in the Czech Republic to determine input–output element fluxes in semi-natural forest ecosystems recovering from anthropogenic acidification. The network consists from 16 catchments and the primary observations of elements fluxes were complemented by monitoring of biomass stock, element pools in soil and vegetation, and the main water balance components. Over last three decades, reductions of SO2, NOx and NH3 emissions were followed by sulphur (S) and nitrogen (N) deposition reductions of 75% and 30%, respectively. Steeper declines of strong acid anion concentrations compared to cations (Ca, Mg, Na, K, NH4) in precipitation resulted in precipitation pH increase from 4.5 to 5.2 in bulk precipitation and from 4.0 to 5.1 in spruce throughfall. Stream chemistry responded to changes in deposition: S leaching declined. However at majority of catchments soils acted as a net source of S to runoff, delaying recovery. Stream pH increased at acidic streams (pH < 6) and aluminium concentration decreased. Stream nitrate (NO3) concentration declined by 60%, considerably more than N deposition. Stream NO3 concentration was tightly positively related to stream total dissolved nitrogen to total phosphorus (P) ratio, suggesting the role of P availability on N retention. Trends in dissolved organic carbon fluxes responded to both acidification recovery and to runoff temporal variation. An exceptional drought occurred between 2014 and 2019. Over this recent period, streamflow decreased by ≈ 40% on average compared to 1990s, due to the increases of soil evaporation and vegetation transpiration by ≈ 30% and declines in precipitation by ≈ 15% on average across the elevational gradient. Sharp decreases of stream runoff at catchments <650 m a.s.l. corresponded to areas of recent forest decline caused by bark beetle infestation on drought stressed spruce forests. Understanding of the interactions among legacies of acidification and eutrophication, drought effects on the water cycle and forest disturbance dynamics is requisite for effective management of forested ecosystems under anthropogenic influence.  相似文献   
29.
湖泊或海湾中的沉积物吸附氮(N)、磷(P)等元素所形成的沉积层成为水体富营养化的內源。在波浪作用下,尤其是强浪作用下,沉积物中的N、P会通过内源释放作用大量进入水体中。本文在自制的U型水槽中开展实验,采用不同水头差来模拟波浪的循环荷载作用,研究了沉积层中的N、P在静置固结状态(Ⅰ)、加波未液化状态(Ⅱ)、加波液化状态(Ⅲ)下的释放规律,并给出该试验条件下的沉积物释放速率的拟合方程。试验结果表明:沉积物中总氮(TN)和溶解性总氮(TDN)的释放速率会随着水动力作用的增强而增加;总磷(TP)、溶解性总磷(TDP)和活性磷酸盐(SRP)的释放速率也随着水动力作用增强而增加,但水体中悬浮物(SS)含量过高会限制其释放速率。  相似文献   
30.
This work presents new 87Sr/86Sr and δ88/86SrSRM987 isotopic values of thirteen mineral, vegetal and animal reference materials. Except for UB‐N, all our results are consistent with previously published data. Our results highlight intermediate precisions among the best presently published and a non‐significant systematic shift with the calculated δ88/86SrSRM987 mean values for the three most analysed reference materials in the literature (i.e., IAPSO, BCR‐2 and JCp‐1). By comparison with the literature and between two distinct digestions, a significant bias of δ88/86SrSRM987 values was highlighted for two reference materials (UB‐N and GS‐N). It has also been shown that digestion protocols (nitric and multi‐acid) have a moderate impact on the δ88/86SrSRM987 isotopic values for the Jls‐1 reference materials suggesting that a nitric acid digestion of carbonate can be used without significant bias from partial digestion of non‐carbonate impurities. Different δ88/86SrSRM987 values were measured after two independent Sr/matrix separations, according to the same protocol, for a fat‐rich organic reference material (BCR‐380R) and have been related to a potential post‐digestion heterogeneity. Finally, the δ88/86SrSRM987 value differences measured between animal‐vegetal and between coral‐seawater reference materials agree with the previously published results, highlighting an Sr isotopic fractionation along the trophic chain and during carbonate precipitation.  相似文献   
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