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81.
该种方法利用离子色谱仪的电导检测器与电化学检测器串联 ,十几分钟即可连续完成水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3 的测定 ,方法具有快速、高效、方便、灵敏、选择性好等特点。方法的检出限分别为 :S2 - 12 5 μg/L ;SO2 - 3 2 2 4 μg/L ;SO2 - 45 0 μg/L ;S2 O2 - 35 0 μg/L。相对标准偏差在 1 5 %~ 6 9%之间 ,能够满足水中S2 - 、SO2 - 3 、SO2 - 4、S2 O2 - 3四种阴离子分析测试的需要。 相似文献
82.
农田生态系统温室气体排放研究进展 总被引:39,自引:0,他引:39
自1985年起,中国科学院大气物理研究所利用自行设计制造的自动观测仪器系统,历时十六年先后对我国四大类主要水稻产区的甲烷排放规律及其与土壤、气象条件和农业管理措施的关系进行了系统野外观测实验,并对稻田甲烷产生、转化和输送机理进行了理论研究,探讨了控制稻田甲烷排放的实用措施,建立了估算和预测稻田甲烷排放的数值模型.在甲烷排放的时空变化规律和转化率研究方面有一系列新的发现,在稻田甲烷产生率、排放率及其与环境条件的关系方面取得一系列新的成果,以充分证据改变了国际上关于全球和中国稻田甲烷排放总量的估算.在对稻田甲 相似文献
83.
Olaf?Brockamp Norbert?Clauer Michael?ZutherEmail author 《International Journal of Earth Sciences》2003,92(6):843-851
A fossil geothermal area is hosted by the Carboniferous, Permian and Bunter sandstones of the Offenburg intramontane trough in the central Black Forest. The hydrothermal alteration is identified on the basis of newly formed sericites, which appear as pseudomorphs after feldspar and filling of pore spaces. According to K–Ar dating of sericite, serititization occurred about 145 Ma ago (Jurassic). On the basis of ORDER="0">18O analyses of sericite, sericite composition and vitrinite reflectance, the hydrothermal fluids had temperatures of 150–210 °C. Because their electrolyte content was low, these fluids are assumed to have derived from meteoric water. A second pulse of electrolyte-rich hydrothermal fluids resulted in quartz overgrowths. Fluid mobilization seems to be linked to the disintegration of Pangaea and to reactivated fault systems extending from the crystalline basement into the intramontane sediments. 相似文献
84.
Fluxes of CO<Subscript>2</Subscript>, CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O from alpine grassland in the Tibetan Plateau 总被引:1,自引:0,他引:1
PEIZhiyong OUYANGHua ZHOUCaiping XUXingliang 《地理学报(英文版)》2003,13(1):27-34
Using static chamber technique,fluxes of CO2,CH4 and N2O were measured in the alpine grassland area from July 2000 to July 2001,determinations of mean fluxes showed that CO2 and N2O were generally released from the soil,while the alpine grassland accounted for a weak CH4 sink.Fluxes of CO2,CH4 and N2O ranged widely.The highest CO2 emission occurred in August,whereas almost 90?of the whole year emission occurred in the growing season.But the variations of CH4 and N2O fluxes did not show any clear patterns over the one-year-experiment.During a daily variation,the maximum CO2 emission occurred at 16:00,and then decreased to the minimum emission in the early morning.Daily pattern analyses indicated that the variation in CO2 fluxes was positively related to air temperatures(R^2=0.73)and soil temperatures at a depth of 5 cm(R^2=0.86),whereas daily variations in CH4 and N2O fluxes were poorly explained by soil temperatures and climatic variables.CO2 emissions in this area were much lower than other grasslands in plain areas. 相似文献
85.
宁芜盆地凹山和东山铁矿床流体包裹体和氢氧同位素研究 总被引:6,自引:4,他引:6
本文对宁芜地区凹山和东山铁矿床中的磷灰石流体包襄体进行了较为系统的测温研究,并测定了不同时期形成的磁铁矿、阳起石和石英的 H、O 同位素组成。凹山和东山铁矿磷灰石含有丰富的流体包裹体,原生气液包裹体包括早期细长管状、针状包裹体(类型Ⅱ)和晚期不规则状包襄体(类型Ⅰ);早期包裹体又可分为单一液相包裹体(类型Ⅱ-a)、气液两相(富气相)包襄体(类型Ⅱ-b)、气液两相(富液相)包裹体(类型Ⅱ-c)和气相、液相及固相多相包裹体(类型Ⅱ-d)四种亚类。包襄体中至少含有五种不同的子矿物。磷灰石包裹体记录了多个峰值温度,从600℃~800℃到~410℃和~270℃,分别对应于磷灰石(磁铁矿 透辉石)、阳起石和石英的形成。流体的盐度随温度的降低而逐渐减小,从高达~80%NaCl equiv。到<20%NaCl equiv。磷灰石形成时流体处于不均匀的状态,流体包裹体为非均一捕获。H、O 同位素研究显示成矿流体早期为演化的初始岩浆(水),在高温下形成了铁矿石;此后,成矿流体有可能与蒸发盆地卤水或大气降水发生混合;晚期则可能有较显著的大气降水加入。 相似文献
86.
Expeditions to Muztagata (in the eastern Pamirs) during the summer seasons of 2002 and 2003 collected precipitation samples
and measured their oxygen isotopes. The δ
18O in precipitation displays a wide range, varying from −17.40‰ to +1.33‰ in June-September 2002 and from −22.31‰ to +4.59‰
in May-August 2003. The δ
18O in precipitation correlates with the initial temperature of precipitation during the observing periods. The positive correlation
between δ
18O and temperature suggests that δ
18O can be used as an indicator of temperature in this region. The δ
18O values in fresh-snow samples collected from two snow events at different elevations on the Muztagata Glacier show a strong
“altitude effect”, with a ratio of nearly −0.40% per 100 m from 5500 m to 7450 m. 相似文献
87.
Expeditions during the summers of 2002 and 2003 implemented continuous monitoring of near-surface (2 m height) atmospheric
CO2 and H2O concentrations at the 4500 m elevation on Muztagata. The resultant data sets reveal a slight decrease of CO2 concentrations (of about 5 μmol·mol-1) and changes in the diurnal variations from the end of June to the middle August. The daily maximum CO2 concentrations occur between 02:30-05:30 AM (local time) and the minimum levels occur between 12:00-15:30 PM. The atmospheric
CO2 concentrations in the summer of 2002 were around 5 μmol·mol-1 lower than those during the same period of 2003, whereas the diurnal amplitude was higher. In contrast, we found that the
daily mean atmospheric H2O content in 2003 was much lower than that in 2002 and there exists a striking negative correlation between CO2 and H2O concentrations. We therefore suggest that the near-surface atmospheric CO2 concentration is affected not only by photosynthesis and respiration, but also by the air H2O content in the glaciated region around Muztagata. 相似文献
88.
氮氧同位素在河流硝酸盐研究中的应用 总被引:9,自引:0,他引:9
多年来,世界各地河流普遍存在硝酸盐污染问题。为控制河流的硝酸盐污染,确定河水中硝酸盐的来源以及研究氮的循环过程就显得尤为重要。由于在不同成因下,硝酸盐的δ15N和δ18O存在着较大差异,因此利用氮、氧同位素方法研究河流硝酸盐问题正日益受到国内外研究人员的重视。综述了用硝酸盐中氮、氧同位素来研究河流硝酸盐的不同来源(大气沉降、化肥、牲畜粪、土壤硝酸盐等)和示踪其地球化学循环过程,特别是反硝化过程,这两方面的研究进展,并对我国河流硝酸盐研究现状进行了讨论及提出今后的研究方向。 相似文献
89.
A combined study of mineral O isotopes and hydroxyl contents was carried out for the contacts between ultrahigh‐pressure eclogite and gneiss from main hole of the Chinese Continental Scientific Drilling Project in the Sulu orogen. While there is a large δ18O variation from ?8.3 to 7.3‰ for all minerals, different styles of mineral‐pair fractionation occur at the boundaries of different lithologies. Both equilibrium and disequilibrium O isotope fractionations are observed between quartz and the other minerals, with reversed fractionations between omphacite and garnet in some samples of eclogite. This suggests that both eclogite and gneiss acquired their negative δ18O values by meteoric‐hydrothermal alteration of their protoliths at high temperatures before subduction, and that fluid‐assisted O isotope exchange did take place across the boundary of different lithologies at local scales during amphibolite‐facies retrogression. Fourier Transform Infrared Spectroscopy analysis yielded H2O concentrations of 50 to 1144 p.p.m. (by weight) for garnet and 139 to 751 p.p.m. for omphacite. The state of equilibrium or disequilibrium O isotope fractionations between omphacite and garnet are correlated with variations in their water content at local scales, indicating that the internally derived fluid plays a critical role in retrograde metamorphism during exhumation. The retrograde metamorphism results in mineral reactions and O isotope disequilibria between some of the minerals, but the fluid for retrogression was derived from the decompression exsolution of structural hydroxyl and thus internally buffered in the O isotope composition. A quantitative estimate suggests that a hand specimen (3 × 6 × 9 cm) of eclogite composed of 70% garnet and 30% omphacite can release 0.316 g water by the decompression exsolution of structural hydroxyl, which can form 14.4 g amphibole during exhumation. This provides sufficient amounts of water for the amphibolite‐facies retrogression. 相似文献
90.
WEI Ran WANG Yitian MAO Jingwen HU Qiaoqing QIN Siting LIU Shengyou YE Dejin YUAN Qunhu DOU Ping 《《地质学报》英文版》2020,94(4):884-900
The extensive Changba-Lijiagou Pb-Zn deposit is located in the north of the Xihe–Chengxian ore cluster in West Qinling. The ore bodies are mainly hosted in the marble, dolomitic marble and biotite-calcite-quartz schist of the Middle Devonian Anjiacha Formation, and are structurally controlled by the fault and anticline. The ore-forming process can be divided into three main stages, based on field geological features and mineral assemblages. The mineral assemblages of hydrothermal stage I are pale-yellow coarse grain, low Fe sphalerite, pyrite with pits, barite and biotite. The mineral assemblages of hydrothermal stage II are black-brown cryptocrystalline, high Fe shalerite, pyrite without pits, marcasite or arsenopyrite replace the pyrite with pits, K-feldspar. The features of hydrothermal stage III are calcite-quartz-sulfide vein cutting the laminated, banded ore body. Forty-two sulfur isotope analyses, twenty-five lead isotope analyses and nineteen carbon and oxygen isotope analyses were determined on sphalerite, pyrite, galena and calcite. The δ34 S values of stage I(20.3 to 29.0‰) are consistent with the δ34 S of sulfate(barite) in the stratum. Combined with geological feature, inclusion characteristics and EPMA data, we propose that TSR has played a key role in the formation of the sulfides in stage I. The δ34 S values of stage II sphalerite and pyrite(15.1 to 23.0‰) are between sulfides in the host rock, magmatic sulfur and the sulfate(barite) in the stratum. This result suggests that multiple S reservoirs were the sources for S2-in stage II. The δ34 S values of stage III(13.1 to 22‰) combined with the structure of the geological and mineral features suggest a magmatic hydrothermal origin of the mineralization. The lead isotope compositions of the sulfides have 206 Pb/204 Pb ranging from 17.9480 to 17.9782, 207 Pb/204 Pb ranging from 15.611 to 15.622, and 208 Pb/204 Pb ranging from 38.1368 to 38.1691 in the three ore-forming stages. The narrow and symmetric distributions of the lead isotope values reflect homogenization of granite and mantle sources before the Pb-Zn mineralization. The δ13 CPDB and δ18 OSMOW values of stage I range from-0.1 to 2.4‰ and from 18.8 to 21.7‰. The values and inclusion data indicate that the source of fluids in stage I was the dissolution of marine carbonate. The δ13 CPDB and δ18 OSMOW values of stage II range from-4 to 1‰ and from 12.3 to 20.3‰, suggesting multiple C-O reservoirs in the Changba deposit and the addition of mantle-source fluid to the system. The values in stage III are-3.1‰ and 19.7‰, respectively. We infer that the process of mineralization involved evaporitic salt and sedimentary organic-bearing units interacting through thermochemical sulfate reduction through the isotopic, mineralogy and inclusion evidences. Subsequently, the geology feature, mineral assemblages, EPMA data and isotopic values support the conclusion that the ore-forming hydrothermal fluids were mixed with magmatic hydrothermal fluids and forming the massive dark sphalerite, then yielding the calcite-quartz-sulfide vein ore type at the last stage. The genesis of this ore deposit was epigenetic rather than the previously-proposed sedimentary-exhalative(SEDEX) type. 相似文献