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81.
矿物材料合成的直流弧光法   总被引:1,自引:0,他引:1  
阐述了Ar+H2+CH4气体体系中直流弧光放电过程,及其在金刚石膜等矿物材料合成中的应用。  相似文献   
82.
山西铝土矿矿石中鲕、豆、碎屑等组构均具红土性质,结合化学成分特征、稀土元素特征、氧同住素特征、锆石等副矿物特征及含矿岩系底部岩层与下伏中奥陶纪灰岩关系和矿床分布与古陆、古岛的依赖关系等方面分析,铝土矿的成矿物质多是异源的,多为古陆上的铝硅酸盐岩红土风化产物,经流水以机械碎屑形式被搬运至海盆,沉积成矿  相似文献   
83.
着重介绍了间隔式钻孔灌注桩在挡土护坡技术中的应用方法,设计时的主要参考依据,计算土压力理论的应用原则以及施工中需注意的几个问题,为进行深基础挡土护坡的工程提供了部分参考依据。  相似文献   
84.
李艺 《矿产与地质》2004,18(1):42-45
新材料是发展高新技术产业的基础。根据广西的矿产资源优势和在矿物材料方面的研究基础和技术力量,提出了加强工艺矿物学研究,大力发展广西新型矿物材料的研究开发方向,特别提出了超细改性矿物粉体材料、环保矿物材料、节能保温矿物材料、高技术陶瓷材料和合成矿物晶体材料等材料体系中的重点开发方向。  相似文献   
85.
The simultaneous eruption in 1996 of andesite from Karymskyvolcano and of basalt from the Academy Nauk vent 6 km away appearsto provide a case of mafic recharge of an andesite reservoirfor which the time of recharge is exactly known and direct samplesof the recharging magma are available. The explosive phreato-magmaticeruption of basalt was terminated in less than 24 h, whereasandesite erupted continuously during the following 4 years.Detailed petrological study of volcanic ash, bombs and lavasof Karymsky andesite erupted during the period 1996–1999provides evidence for basaltic replenishment at the beginningof the eruptive cycle, as well as a record of compositionalvariations within the Karymsky magma reservoir induced by basalticrecharge. Shortly after the beginning of the eruption the compositionof the matrix glass of the Karymsky tephra became more maficand then, within 2 months, gradually returned to its originalstate and remained almost constant for the following 3 years.Further evidence for basaltic replenishment is provided by thepresence of xenocrysts of basaltic origin in the andesite ofKarymsky. A conspicuous portion of the plagioclase phenocrystsin the Karymsky andesite has calcic cores, with compositionsand textures resembling those of plagioclases in the AcademyNauk basalt. Similarly, the earlier portion of the andesiteof the eruption sequence contains rare olivines, which occuras resorbed cores in pyroxenes. The composition of the olivinematches that of olivines in the Academy Nauk basalt. The sequenceof events appears to be: (1) injection of basaltic magma intothe Karymsky chamber with immediate, compensating expulsionof pre-existing chamber magma from the Karymsky central vent;(2) direct mixing of basaltic and andesitic magmas with dispersalof phenocrysts associated with the basalt throughout the andesiteso that newly mixed magma appeared at the vent within 2 months;(3) re-establishment of thermal and chemical equilibrium withinthe reservoir involving crystallization in the new hybrid liquid,which returned the melt composition to ‘normal’,formed rims on inherited calcic plagioclase, and caused theresorption of dispersed olivine xenocrysts. Taken together,these findings indicate that the Karymsky magma reservoir wasrecharged by basalt at the onset of the 1996 eruptive cycle.The rapidity and thoroughness of mixing of the basalt with thepre-existing andesite probably reflects the modest contrastin temperature, viscosity, and density between the two magmas. KEY WORDS: Karymsky; Kamchatka; magma mixing; andesite; volcanic glass; plagioclase  相似文献   
86.
Wavelength dispersive X-ray fluorescence spectrometry (WD-XRF) is widely used for the analysis of soils and sediments using well characterised procedures. However, difficulties can occur with samples such as unknowns containing small amounts of ore materials and samples collected from contaminated sites where trace elemental concentrations can exceed the concentration range for routine analysis. We studied the performance of a commercially available method, based on fundamental parameters (FP) to correct matrix effects. The spectrometer was originally calibrated with elemental or simple compound calibrants. Samples were analysed as pressed powder pellets. Eighteen sediment and soil reference materials, three of them with certified values for some of their constituents, were used to evaluate accuracy, by comparing results with recommended values and their standard deviations (RV ± 2s) or certified values and their confidence intervals (CV ± Cl). When results fell systematically outside these intervals, calibrations were refined with geochemical reference materials. The best agreement of results with recommended and certified values was obtained when the contents of H2O and C in each sample were included as matrix constituents during calculations. The detection limits of trace elements tended to be relatively high, because the measuring conditions employed were not maximised for sensitivity. The main advantage of the method tested was that it enabled the analysis of samples with high concentrations of trace elements and the determination of elements such as F, Bi, Sb and W, which are not commonly included in quantitative XRF analysis of geological samples.  相似文献   
87.
This contribution aims to report the reflections we had with the scientific community during two international workshops on reference materials for stable isotopes in Davos (2002) and Nice (2003). After evaluating the isotopic homogeneity of some existing reference materials, based on either certificates, literature data or specific inter-laboratory rounds, we confirm these as primary reference materials or propose new ones relative to which stable isotope compositions should be reported. We propose DSM-3 for Mg, NIST SRM 915a for Ca, L-SVEC for Li and NBS28 for Si. Cadmium does not yet have a well identified delta zero material, although three commercial mono-elemental Cd solutions have yielded the same isotopic composition relative to one another. In order to scale the linearity of any mass spectrometer, some secondary reference materials are also proposed: Cambridge-1 solution for Mg, the "Münster-Cd" and JEPPIM Cd solutions for Cd and the "Big Batch" silicate for Si. The team from Nancy propose to prepare a mixed spike solution for Li isotopes. Well-characterised natural samples such as ocean or continental waters, diatoms, sponges, rocks and minerals are needed to validate the entire analytical procedure, particularly to take into account the effect of sample mineralisation and of chemical manipulations for elemental separation prior to analysis.  相似文献   
88.
The Li isotope ratios of four international rock reference materials, USGS BHVO-2, GSJ JB-2, JG-2, JA-1 and modern seawater (Mediterranean, Pacific and North Atlantic) were determined using multi-collector inductively coupled plasma-mass spectrometry (MC-ICP-MS). These reference materials of natural samples were chosen to span a considerable range in Li isotope ratios and cover several different matrices in order to provide a useful benchmark for future studies. Our new analytical technique achieves significantly higher precision and reproducibility (< ± O.3%o 2s) than previous methods, with the additional advantage of requiring very low sample masses of ca . 2 ng of Li.  相似文献   
89.
A key geodetic contribution to both the three Global Observing Systems and initiatives like the European Global Monitoring for Environment and Security is an accurate, long-term stable, and easily accessible reference frame as the backbone. Many emerging scientific as well as non-scientific high-accuracy applications require access to an unique, technique-independent reference frame decontaminated for short-term fluctuations due to global Earth system processes. Such a reference frame can only be maintained and made available through an observing system such as the Global Geodetic Observing System (GGOS), which is currently implemented and expected to provide sufficient information on changes in the Earth figure, its rotation and its gravity field. Based on a number of examples from monitoring of infrastructure, point positioning, maintenance of national references frames to global changes studies, likely future accuracy requirements for a global terrestrial reference frame are set up as function of time scales. Expected accuracy requirements for a large range of high-accuracy applications are less than 5 mm for diurnal and sub-diurnal time scales, 2–3 mm on monthly to seasonal time scales, better than 1 mm/year on decadal to 50 years time scales. Based on these requirements, specifications for a geodetic observing system meeting the accuracy requirements can be derived.  相似文献   
90.
New glass reference materials GSA-1G, GSC-1G, GSD-1G and GSE-1G have been characterised using a prototype solid state laser ablation system capable of producing wavelengths of 193 nm, 213 nm and 266 nm. This system allowed comparison of the effects of different laser wavelengths under nearly identical ablation and ICP operating conditions. The wavelengths 213 nm and 266 nm were also used at higher energy densities to evaluate the influence of energy density on quantitative analysis. In addition, the glass reference materials were analysed using commercially available 266 nm Nd:YAG and 193 nm ArF excimer lasers. Laser ablation analysis was carried out using both single spot and scanning mode ablation. Using laser ablation ICP-MS, concentrations of fifty-eight elements were determined with external calibration to the NIST SRM 610 glass reference material. Instead of applying the more common internal standardisation procedure, the total concentration of all element oxide concentrations was normalised to 100%. Major element concentrations were compared with those determined by electron microprobe. In addition to NIST SRM 610 for external calibration, USGS BCR-2G was used as a more closely matrix-matched reference material in order to compare the effect of matrix-matched and non matrix-matched calibration on quantitative analysis. The results show that the various laser wavelengths and energy densities applied produced similar results, with the exception of scanning mode ablation at 266 nm without matrix-matched calibration where deviations up to 60% from the average were found. However, results acquired using a scanning mode with a matrix-matched calibration agreed with results obtained by spot analysis. The increased abundance of large particles produced when using a scanning ablation mode with NIST SRM 610, is responsible for elemental fractionation effects caused by incomplete vaporisation of large particles in the ICP.  相似文献   
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