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131.
西安南郊丰水年秋季土壤水分研究 总被引:4,自引:0,他引:4
通过对西安南郊丰水年秋季土壤含水量的测定,研究了地下0~6 m之间土壤含水量的变化与土壤干层的恢复问题。研究结果表明,丰水年西安南郊人工林下2~3 m的土壤含水量在20%左右,远远高于正常年份的土壤含水量,而且大于表层和深层的土壤含水量。分析得出,土壤干层发育较弱的地区在降水丰富的年份可以得到一定程度的恢复;西安地区基本适合进行人工造林;通过人工措施,增强降水入渗和土壤含水量,对树木成活和长期的生长应当具有明显的作用。 相似文献
132.
近50 a渭河流域洪水成因分析及防治对策 总被引:6,自引:1,他引:6
通过对近50 a渭河流域洪水的年际变化、月际变化和潼关高程变化的综合分析得出,造成该流域洪水灾害的原因有降水量年内分配不均和年际变化大,滩面淤积加重,支流河口淤塞以及河势、流态的恶化等。针对这些原因,根据渭河流域洪水灾害的特点,提出了相应的防治措施,即降低下游高程,减少河道的淤积,增大河道泄洪能力;利用水库进行调水调沙,引进客水冲刷渭河下游;防洪工程要除险加固,提高防洪标准与抗洪能力;恢复林草植被,遏止水土流失,从源头上控制泥沙入河等。 相似文献
133.
Fluid sources for the La Guitarra epithermal deposit (Temascaltepec district, Mexico): Volatile and helium isotope analyses in fluid inclusions 总被引:1,自引:0,他引:1
Antoni Camprubí Beverly A. Chomiak Ruth E. Villanueva-Estrada David I. Norman Martin Stute 《Chemical Geology》2006,231(3):252-284
The La Guitarra deposit (Temascaltepec district, South-Central Mexico), belongs to the low/intermediate sulfidation epithermal type, has a polymetallic character although it is currently being mined for Ag and Au. The mineralization shows a polyphasic character and formed through several stages and sub-stages (named I, IIA, IIB, IIC, IID, and III). The previous structural, mineralogical, fluid inclusion and stable isotope studies were used to constrain the selection of samples for volatile and helium isotope analyses portrayed in this study. The N2/Ar overall range obtained from analytical runs on fluid inclusion volatiles, by means of Quadrupole Mass Spectrometry (QMS), is 0 to 2526, and it ranges 0 to 2526 for stage I, 0 to 1264 for stage IIA, 0 to 1369 for stage IIB, 11 to 2401 for stage IIC, 19 to 324 for stage IID, and 0 to 2526 for stage III. These values, combined with the CO2/CH4 ratios, and N2-He-Ar and N2-CH4-Ar relationships, suggest the occurrence of fluids from magmatic, crustal, and shallow meteoric sources in the forming epithermal vein deposit. The helium isotope analyses, obtained by means of Noble Gas Mass Spectrometry, display R/Ra average values between 0.5 and 2, pointing to the occurrence of mantle-derived helium that was relatively diluted or “contaminated” by crustal helium. These volatile analyses, when correlated with the stable isotope data from previous works and He isotope data, show the same distribution of data concerning sources for mineralizing fluids, especially those corresponding to magmatic and crustal sources. Thus, the overall geochemical data from mineralizing fluids are revealed as intrinsically consistent when compared to each other.The three main sources for mineralizing fluids (magmatic, and both deep and shallow meteoric fluids) are accountable at any scale, from stages of mineralization down to specific mineral associations. The volatile and helium isotope data obtained in this paper suggest that the precious metal-bearing mineral associations formed after hydrothermal pulses of predominantly oxidized magmatic fluids, and thus it is likely that precious metals were carried by fluids with such origin. Minerals from base-metal sulfide associations record both crustal and magmatic sources for mineralizing fluids, thus suggesting that base metals could be derived from deep leaching of crustal rocks. At the La Guitarra epithermal deposit there is no evidence for an evolution of mineralizing fluids towards any dominant source. Rather than that, volatile analyses in fluid inclusions suggest that this deposit formed as a pulsing hydrothermal system where each pulse or set of pulses accounts for different compositions of mineralizing fluids.The positive correlation between the relative content of magmatic fluids (high N2/Ar ratios) and H2S suggests that the necessary sulfur to carry mostly gold as bisulfide complexes came essentially from magmatic sources. Chlorine necessary to carry silver and base metals was found to be abundant in inclusion fluids and although there is no evidence about its source, it is plausible that it may come from magmatic sources as well. 相似文献
134.
Yunchao HAO Zhigang GUO Dejiang FAN 《中国地球化学学报》2006,25(B08):13-13
In the East China Sea (ECS), there are some mud areas, including the south coastal mud area, the north coastal mud area, and the mud area to the southwest of Cheju Island. X-ray fluorescence (XRF) techniques and Thermal Ionization Mass Spectrometry (TIMS) were used to study the high-resolution sedimentary record of Pb concentrations and Pb stable isotopic compositions in the past one hundred and fifty years in the coastal mud of the ECS. Pb concentrations of a ^210Pb dating S5 core in the study area have increased rapidly since 1980, and reached the maximal value with 65.08 μg/g in 2000, corresponding to the fast economic development of China since the implementation of the "Reform and Open Policy" in 1978; ^206Pb/^207Pb ratios generally had stabilized at 1.195 from 1860 to 1966, and decreased gradually from 1966 to 2000, indicating that the anthropogenic source Pb contribution to the ECS has increased gradually since 1966, especially since 1980. Pb concentrations decreased distinctly from 2000 to 2003 and ^206Pb/^207Pb ratios increased from 2001 to 2003, corresponding closely to the ban of lead gasoline from 2000 in China. From 1950 to 2003, there occurred four distinct decrease events of ^206Pb/^207Pb, possibly responding to the Changjiang River (Yangtze River) catastrophic floods in 1998, 1991, 1981 and 1954; from 1860 to 1966, there were two decrease periods of ^206Pb/^207Pb, which may respond to the catastrophic floods of Changjiang River in 1931 and 1935, and 1870. As a result of the erosion and drowning by the catastrophic floods, the anthropogenic lead accumulated in soil and water environments over a long period of time was brought into the Changjiang River, then part of them was finally transported into the ECS, which leads to changes in Pb stable isotopic composition. 相似文献
135.
地应力测量在矿床突水防治中的应用——以河南夹沟铝土矿床突水防治工程为例 总被引:2,自引:0,他引:2
针对铝土矿床突水,开展地应力测量研究,是分析查明突水成因、优化确定防治方案及合理进行矿床底板管理的一项重要手段。夹沟矿床测量分析结果表明:①矿床地区存在较高的水平构造应力,其量值明显高于垂向应力。矿床水平高构造应力对矿床底板及其边坡稳定性具有不良影响,矿床开采掘面轴线走向应沿N70°E方向布设趋佳;②由于持续开采作用,矿床附近地应力状态产生不良扰动,水平高构造应力同开采形成的局部地应力场不良改变的叠加影响对矿床底板岩石场各类裂隙、结构面水起到极为重要的“催化”作用,是造成矿床底板突水的重要因素之一;③防治工作应重视加强矿床底板管理,科学预留安全隔水层屏障。并建议对矿床底板及其下伏一定范围内的灰岩实施预注浆处理,使得裂隙得以加固、溶洞得到堵塞,以抵抗不良应力的作用,消除或减弱对矿床突水的影响。 相似文献
136.
137.
Etienne Deloule 《Geostandards and Geoanalytical Research》2006,30(3):175-182
This review of the literature from 2004 and 2005 concerning secondary ion mass spectrometry (SIMS) highlights the contribution the technique has made in the fields of petrology, geochronology, cosmochemistry and material sciences. In petrology, much research was devoted to the measurement of stable isotopes and trace elements by developments in multicollection acquisition, with emphasis on low atomic mass number elements. Elements studied in particular were S (in sulfides), O (in garnets), C (in sedimentary organic matter), Cl (in glasses) and Si. Novel applications of SIMS to geochronology have included the measurement of young zircon grains by the U-Pb and U-Th decay methods. An increasing number of studies have combined U-Pb geochronology with the measurement of trace elements or stable isotopes in zircon. 相似文献
138.
长白山锦北雨养泥炭剖面元素富集规律分析 总被引:3,自引:2,他引:3
为了揭示长白山锦北泥炭沼泽区泥炭沉积环境和重金属元素的历史变化及其对环境的指示意义,利用荷兰W ardenaar泥炭采样器采取泥炭样品并对样品进行高分辨率切割。用原子吸收分光光度计和等离子体发射光谱仪测定不同深度剖面Ca,Mg,Na,K,A l,Ti,Cu,Zn,Fe,Mn,Pb,Cr,N i和Co的浓度。研究分析了Ca,Mg,Na,K,A l,Ti,Mn,Zn,Cu,Pb,Cr,N i和Co在泥炭剖面的分布趋势并对其进行了相关分析和富集分析,得出Mn,Zn,Cu,Pb,Cr,N i和Co呈显著相关且在泥炭表层明显累积,揭示出泥炭表层重金属元素的大气沉降来源,表明近年来人类重金属消耗量及排放量的增加是大气沉降重金属元素的主要释放源,而且环境中重金属污染有加重的趋势。 相似文献
139.
Edward Derbyshire 《中国地球化学学报》2006,25(B08):219-219
Fine atmospheric dust includes mineral particles and aggregates, fibrous minerals and fibrous organic material. Generation, dislodgement and transport (deflation) of natural dust with the finer (〈4 microns) components suspended as silt-size aggregates, is widespread in and adjacent to the world's drylands, as well as deriving from volcanic vents. Silica is a highly fibrogenic agent in lung tissue. Long-term inhaling of siliceous dusts can lead to a number of fibrotic lung diseases, including natural (non-occupational) pneumoconioses (notably silicosis, but including asbestosis and others). Different polymorphs of silica show different levels of toxicity in interaction with lung tissue. Particles with highly active surfaces may release radicals, causing cell damage. Some types of inhaled particulates are degraded by macrophages, but many are highly resistant and persist in the lungs, some stimulating fibroblastic cells to deposit collagen. Silicosis is an inflammation of the lung commonly caused by silicate mineral particles, leading to fibrosis. Three types are recognized: nodular pulmonary fibrosis (simple or chronic silicosis), acute silicosis, and accelerated silicosis. Generally, finer particulates have greater oxidative capacity than the coarser fractions. They contain more reactive oxygen species, their greater bioreactivity making them more toxic to pulmonary tissue. Nevertheless, inhalation of large dust particles (〉 10μm) may constitute a health risk if the mineralogy is toxic, regardless of where the grains lodge in the respiratory system. Dust may absorb harmful gases, disease-generating bacteria and carcinogenic hydrocarbon compounds. Silica-related respiratory disease may also an exacerbate cardiac problem, and epidemiology suggests a link with tuberculosis. Quantification of dust loading and exposure requires study of spatial and temporal patterns, supported by meteorological analysis, airflow modeling and satellite-borne imagery. Some acute, short-term health impacts have been assessed using atmospheric and health records both before and after a dust storm or by comparison of populations within and outside such events. Analysis of the size, shape, mineralogy and geochemistry of ambient dust particulates provides information on natural dust sources, dust concentrations, and potential particulate toxicity, as well as providing a datum for assessment of human exposure levels. 相似文献
140.
R. Thomas J.D. Webster D. Rhede W. Seifert K. Rickers H.-J. Frster W. Heinrich P. Davidson 《Lithos》2006,91(1-4):137-149
Fractional crystallization of peraluminous F- and H2O-rich granite magmas progressively enriches the remaining melt with volatiles. We show that, at saturation, the melt may separate into two immiscible conjugate melt fractions, one of the fractions shows increasing peraluminosity and the other increasing peralkalinity. These melt fractions also fractionate the incompatible elements to significantly different degrees. Coexisting melt fractions have differing chemical and physical properties and, due to their high density and viscosity contrasts, they will tend to separate readily from each other. Once separated, each melt fraction evolves independently in response to changing T/P/X conditions and further immiscibility events may occur, each generating its own conjugate pair of melt fractions. The strongly peralkaline melt fractions in particular are very reactive and commonly react until equilibrium is attained. Consequently, the peralkaline melt fraction is commonly preserved only in the isolated melt and mineral inclusions.
We demonstrate that the differences between melt fractions that can be seen most clearly in differing melt inclusion compositions are also visible in the composition of the resulting ore-forming and accessory minerals, and are visible on scales from a few micrometers to hundreds of meters. 相似文献