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991.
中国产业结构变动的碳排放效应研究——基于省级面板数据 总被引:2,自引:0,他引:2
在二氧化碳(CO2)排放影响因素的模型框架内,利用1995—2008年中国省级的面板数据,着重分析产业结构演变对CO2排放的影响。结果表明,产业结构演进决定CO2排放的基本走向,刚性产业结构演进特征使单位CO2排放居高不下;二产主导的产业结构对我国CO2排放产生了明显的增速效应,延缓了CO2排放倒"U"型变化过程。因此,依托低碳经济助推产业结构升级,优化第一、第二产业内部结构,大力发展第三产业,转向低能耗低CO2排放的产业结构是中国低碳经济发展的必由之路。 相似文献
992.
武汉市碳排放的测算及影响因素分解研究 总被引:1,自引:0,他引:1
研究基于14个主要方面碳源,测算了武汉市1996—2009年碳排放量。发现自1996年以来武汉市碳排放呈现"平稳—上升—平稳"的三阶段特征。进一步基于LMDI模型分解碳排放的影响因素,结果表明,能源结构、能源效率因素对碳排放量具有一定抑制作用,但效果不够显著且波动性较强,1997—2009年与基期相比,能源结构、能源效率因素分别累计实现了0.95%,11.30%的碳减排;而经济因素与人口规模因素则对碳排放具有较强推动作用,分别累计产生了64.65%,19.65%的碳增量。最后,据此提出推进武汉市碳减排的对策建议。 相似文献
993.
卡林型金矿石中金的赋存状态分析新方法 总被引:1,自引:1,他引:0
卡林型金矿富含有机质,金主要呈显微一超显微分散状态存在,利用工艺矿物学参数自动检测分析仪(MLA)及传统化学方法只能大致判断矿石中金的赋存趋势,无法对其赋存状态准确定量.本文利用MLA仪器系统分析贵州回龙卡林型金矿,测得矿石中金主要以显微-超显微状态包裹于黄铁矿和毒砂中,少量被脉石等其他矿石包裹;黄铁矿约66%完全解离,而毒砂仅30%完全解离,载金矿物与其他矿物连生或者被包裹,将不利于硫化物包裹金的浸出.结合回龙金矿石中金的赋存特征和富含有机质的特点,对传统的物相分析流程进行改进,调整了硫化物包裹金和碳酸盐包裹金的浸出顺序,提出裸露金-碳酸盐包裹金-硫化物包裹金-硅酸盐包裹金的浸出流程,在裸露金及碳酸盐包裹金浸出时加入活性炭,利用竞争吸附抑制矿石中有机炭对金的吸附,降低有机炭对分相的影响.对比试验结果表明,采用改进的方法,有机炭含量在1%左右的金矿石分相时加入活性炭对各相测定值的影响不大;先浸出碳酸盐包裹金,再测定硫化物包裹金,各相的测定数据更加准确.改进的方法(加活性炭)用于测定回龙金矿中裸露金和碳酸盐、硫化物、硅酸盐包裹金,含量分别为1.25%、84.17%、11.46%和3.13%,与选矿试验结果相一致,表明该法适合应用于卡林型金矿中金的赋存状态分析. 相似文献
994.
泥岩/页岩:中国元古宙—古生代海相沉积盆地主要烃源岩 总被引:1,自引:0,他引:1
在中国元古宙—古生代海相沉积体系中,碳酸盐岩是最主要的沉积岩类型,长期以来研究的重点也一直是碳酸盐岩,对海相泥岩/页岩的关注比较少,并且认为碳酸盐岩是海相沉积盆地中主要的烃源岩。对中国南方上、中、下扬子地区、滇黔桂地区、塔里木盆地、鄂尔多斯盆地、华北地区等147条剖面、289口探井及浅井约11200余个样品有机碳含量的分析与统计表明,泥岩/页岩有机质丰度高,是中国元古宙—古生代海相沉积盆地中主要的烃源岩类型,而碳酸盐岩有机质丰度普遍较低,仅仅是次要的烃源岩类型。海相碳酸盐岩中有机质的含量与碳酸盐含量呈现弱的负相关性,泥质输入有利于形成高有机质丰度的碳酸盐岩烃源岩,但并不是高有机质丰度碳酸盐岩烃源岩发育的必要条件,决定碳酸盐岩烃源岩有机质丰度的主要因素是有机质的生产率、有机质的沉积与保存环境。中国元古宙—古生代海相沉积盆地中并不缺乏高有机质丰度泥岩/页岩类好烃源岩,上、中、下扬子地区主要发育于上震旦统陡山沱组、下寒武统、上奥陶统—下志留统、上二叠统;华南地区主要发育于中、下泥盆统;塔里木盆地主要发育于下寒武统、下奥陶统及中上奥陶统;华北地区为中新元古界洪水庄组、下马岭组。泥灰岩类碳酸盐岩烃源岩在塔里木盆地相对比较发育,在中国南方地区只有下二叠统相对发育。 相似文献
995.
传统认为TSR成因的固态沥青(焦沥青)属于热化学反应的终端产物,不会对TSR的反应进程起到重要作用.本文以活性炭作为固态沥青(焦沥青)的模型化合物,开展了CaSO4-C-H2O体系的热模拟实验研究,探讨了CaSO4-C-H2O体系发生TSR的热力学特征.实验结果表明,CaSO4-C-H2O体系在300℃时即可启动TSR,主要生成CaCO3、H2S和CO2等产物.这一TSR门限温度要远低于以往室内利用气态或液态烃类进行的TSR模拟实验温度范围,与热力学计算结果一致.利用HSC Chemistry 5.0软件进行TSR过程模拟,发现25~200℃时CaSO4-C-H2O体系发生的TSR完全受动力学控制,在温度保持不变情况下,压力增大不利于CaSO4-C-H2O体系发生TSR.较少的含水量对TSR有一定促进作用,而含水量过多则可能抑制TSR的进行,含水量对TSR的影响可能与CaSO4在水中的饱和浓度有关.在一定的温度下,当体系pH≤2时,随着pH逐渐降低,CaSO4的量呈线性递减,但在沉积盆地地层水pH范围内(pH>4),pH对TSR的作用可以忽略不计.CaSO4-C-H2O体系发生的TSR反应是一个放热过程,并且随着温度升高,反应热逐渐增大.在25~200℃范围内,TSR反应热为12.9~133 J/molCaSO4.热力学计算以及模拟实验结果均暗示,固态沥青(焦沥青)可能比烃类更容易参与TSR. 相似文献
996.
André C. Colonese Giovanni Zanchetta Catherine Perlès Russell N. Drysdale Giuseppe Manganelli Ilaria Baneschi Elissavet Dotsika Hélène Valladas 《Quaternary Research》2013
This paper investigates the stable isotopic composition from late Pleistocene–Holocene (~ 13 to ~ 10.5 cal ka BP) shells of the land snail Helix figulina, from Franchthi Cave (Greece). It explores the palaeoclimatic and palaeoenvironmental implications of the isotope palaeoecology of archaeological shells at the time of human occupation of the cave. Modern shells from around the cave were also analysed and their isotopic signatures compared with those of the archaeological shells. The carbon isotope composition of modern shells depicts the consumption of C3 vegetation. Shell oxygen isotopic values are consistent with other Mediterranean snail shells from coastal areas. Combining empirical linear regression and an evaporative model, the δ18Os suggest that modern snails in the study area are active during periods of higher relative humidity and lower rainfall δ18O, probably at night. Late glacial and early Holocene δ18Os show lower values compared to modern ones. Early Holocene δ18Os values likely track enhanced moisture and isotopic changes in the precipitation source. By contrast, lower late glacial δ18O could reflect lower temperatures and δ18Op, compared to the present day. Shell carbon isotope values indicate the presence of C3 vegetation as main source of carbon to late glacial and early Holocene snails. 相似文献
997.
DARIO HARAZIM BAS VAN DE SCHOOTBRUGGE KATRIN SORICHTER JENS FIEBIG ANDRIES WEUG GUILLAUME SUAN WOLFGANG OSCHMANN 《Sedimentology》2013,60(2):359-390
In order to constrain spatial variability in watermass conditions within the European Epicontinental Seaway prior to, during and after the Toarcian Oceanic Anoxic Event, carbon (δ13Cbel, δ13Ccarb) and oxygen (δ18Obel, δ18Ocarb) isotope records were obtained from three sections in the Grands Causses Basin (southern France). These data were then compared with similar records along a north–south transect across the European Epicontinental Seaway. As the conclusions reached here strongly depend on the reliability of belemnite calcites as archives of palaeoceanographic changes, an attempt was made to improve the understanding of isotope signals recorded in belemnite calcite. Intra‐rostral carbon and oxygen‐isotope data from six belemnite specimens belonging to the genus Passaloteuthis were collected. Intra‐rostral carbon‐isotopes are influenced by vital effects, whereas oxygen‐isotopes reflect relative changes in temperature and salinity. Palaeotemperatures calculated from δ18Obel‐isotope records from the Grands Causses Basin confirm relatively low temperatures throughout the Late Pliensbachian. Similar cool water conditions have previously been shown in Germany, England, Spain and Portugal. A temperature increase of up to 6 °C is observed across the Pliensbachian–Toarcian boundary. A pronounced negative shift of at least ?3‰ (Vienna‐Pee Dee Belemnite) is recorded in bulk carbonate carbon during the lower Harpoceras serpentinum zone, typical of the Toarcian Oceanic Anoxic Event. Before and after the Toarcian Oceanic Anoxic Event, a good correlation between δ13Ccarb and δ13Cbel exists, indicating well‐ventilated bottom‐waters and normal marine conditions. Instead, data for the Toarcian Oceanic Anoxic Event indicate the development of a strong north–south gradient in salinity stratification and surface‐water productivity for the Western Tethyan realm. This study thus lends further support to a pronounced regional overprint on carbon and oxygen‐isotope records in epicontinental seaways. 相似文献
998.
萘及烷基萘是原油和沉积有机质的重要组成。目前对于烷基萘单体稳定碳同位素组成随有机质成熟作用加深的演变特征鲜见报道。本研究选取松辽盆地杜601井嫩一段低熟黑色泥岩进行热压模拟生烃实验,采用两步柱色谱层析技术分离烷基萘化合物使其达到稳定碳同位素的在线准确测定,从而厘定有机质不同成熟阶段烷基萘单体稳定碳同位素组成分布面貌。实验结果显示,不同模拟实验温度点排出的一甲基萘(MNs)和二甲基萘(DMNs)各异构体具有相对一致的稳定碳同位素值,分别介于–29.5‰~–29.3‰和–30.9‰~–30.5‰之间,这可能与生烃过程中干酪根的非均一性裂解有关;三甲基萘(TMNs)各异构体之间稳定碳同位素值差异较大,介于–36.8‰~–31.1‰之间,这可能与生源效应有关;其中,1,2,5-TMN稳定碳同位素组成偏轻,介于–36.8‰~–35.6‰之间,可能是细菌来源的藿类化合物降解及其芳构化的产物。实验结果表明,随着有机质热演化作用的加深,烷基萘单体稳定碳同位素组成变化介于0.8‰~1.4‰之间,基本在仪器测试误差范围之内,反映成熟作用所导致的烷基萘单体稳定碳同位素动力学分馏较小。因此,烷基萘单体稳定碳同位素组成可以成为油-源和油-油对比的潜在指标。 相似文献
999.
The differentiated Mesozoic alkali dolerite Prospect Intrusion contains a wide range of secondary minerals, including carbonates (primarily calcite), laumontite, prehnite and heulandite, whose stability relationships imply a formation temperature of <200°C. The δ18O data for carbonates define a higher temperature (160 – 195°C) suite, and a lower temperature (51 – 73°C) suite. The δ13C, δ18O and 87Sr/86Sr isotope systematics for these carbonates suggest derivation of the higher temperature group from magmatic fluids, whereas the other group had a major meteoric component that probably originated from porewater in the country rock. Source fluids for prehnite were meteoric rather than magmatic in origin based on their δD and δ18O ratios. Early in the intrusion's emplacement, CO2-rich hydrothermal fluids formed a carbonate rind sealing the upper part of the hydrothermal system and produced the higher temperature carbonates (calcite) and laumontite. Later, cooler fluids with a meteoric component infiltrated vesicles and fractures, depositing the lower temperature carbonates (calcite, aragonite), heulandite and prehnite. 相似文献
1000.
The Holocene carbonate sequence of perennial North Stromatolite Lake, located adjacent to the Coorong Lagoon near Salt Creek, South Australia, includes a prominent sapropelic unit (7 – 12% total organic carbon), in places more than 2 m thick, that was sampled for the purpose of radiocarbon dating and documenting its diatom and ostracod biostratigraphy. The recovered ostracods were also subjected to carbon and oxygen isotopic analysis. The bulk organic matter at the base of the sapropel yielded an uncalibrated 14C age of 6080 ± 60 y BP. Diatoms, where preserved, are almost exclusively benthic. Stratigraphic variation of the proportions of key indicator species in diatom assemblages records a marked oscillation between oligosaline and eusaline conditions in the hypolimnion during deposition of the sapropel. Ostracod carbon isotope data indicate that the lake at this time was eutrophic, thereby enriching the dissolved inorganic carbon of the hypolimnion in 13C. However, the observed secular variation in δ13C implies a mid-sapropel drop in productivity, caused by a freshening of the lake. Ostracod δ18O values display an overall increase through the sapropel consistent with the rising salinity of the hypolimnion. The existence of a flourishing benthic ostracod community, together with the valve ornamentation of Osticythere baragwanathi, indicates that the bottom waters were well oxygenated. Thus, anoxia was not a prerequisite for sapropel accumulation. The biostratigraphy and chemostratigraphy of the sapropel concur in suggesting a lack of climatic uniformity during its deposition, a period of ~1200 years. This study therefore highlights the potential of diatoms and ostracods in shallow perennial alkaline lakes along the Coorong coastal plain as proxies for short-term (102 – 103 years) Holocene palaeoenvironmental change in southeastern Australia. 相似文献