全文获取类型
收费全文 | 53164篇 |
免费 | 11772篇 |
国内免费 | 17081篇 |
专业分类
测绘学 | 6085篇 |
大气科学 | 9935篇 |
地球物理 | 12317篇 |
地质学 | 30806篇 |
海洋学 | 8561篇 |
天文学 | 1691篇 |
综合类 | 5281篇 |
自然地理 | 7341篇 |
出版年
2024年 | 347篇 |
2023年 | 1035篇 |
2022年 | 2732篇 |
2021年 | 3304篇 |
2020年 | 2652篇 |
2019年 | 3159篇 |
2018年 | 3164篇 |
2017年 | 2813篇 |
2016年 | 3155篇 |
2015年 | 3096篇 |
2014年 | 3381篇 |
2013年 | 3830篇 |
2012年 | 3828篇 |
2011年 | 4029篇 |
2010年 | 4098篇 |
2009年 | 3965篇 |
2008年 | 3844篇 |
2007年 | 3622篇 |
2006年 | 3426篇 |
2005年 | 2885篇 |
2004年 | 2107篇 |
2003年 | 1867篇 |
2002年 | 1687篇 |
2001年 | 1589篇 |
2000年 | 1679篇 |
1999年 | 1755篇 |
1998年 | 1231篇 |
1997年 | 1206篇 |
1996年 | 1069篇 |
1995年 | 900篇 |
1994年 | 850篇 |
1993年 | 721篇 |
1992年 | 589篇 |
1991年 | 445篇 |
1990年 | 353篇 |
1989年 | 303篇 |
1988年 | 273篇 |
1987年 | 197篇 |
1986年 | 167篇 |
1985年 | 123篇 |
1984年 | 84篇 |
1983年 | 68篇 |
1982年 | 83篇 |
1981年 | 60篇 |
1980年 | 31篇 |
1979年 | 43篇 |
1976年 | 15篇 |
1958年 | 29篇 |
1957年 | 14篇 |
1954年 | 20篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
161.
Silicon isotope fractionation in bamboo and its significance to the biogeochemical cycle of silicon 总被引:2,自引:0,他引:2
A systematic investigation on silica contents and silicon isotope compositions of bamboos was undertaken. Seven bamboo plants and related soils were collected from seven locations in China. The roots, stem, branch and leaves for each plant were sampled and their silica contents and silicon isotope compositions were determined. The silica contents and silicon isotope compositions of bulk and water-soluble fraction of soils were also measured. The silica contents of studied bamboo organs vary from 0.30% to 9.95%. Within bamboo plant the silica contents show an increasing trend from stem, through branch, to leaves. In bamboo roots the silica is exclusively in the endodermis cells, but in stem, branch and leaves, the silica is accumulated mainly in epidermal cells. The silicon isotope compositions of bamboos exhibit significant variation, from −2.3‰ to 1.8‰, and large and systematic silicon isotope fractionation was observed within each bamboo. The δ30Si values decrease from roots to stem, but then increase from stem, through branch, to leaves. The ranges of δ30Si values within each bamboo vary from 1.0‰ to 3.3‰. Considering the total range of silicon isotope composition in terrestrial samples is only 7‰, the observed silicon isotope variation in single bamboo is significant and remarkable. This kind of silicon isotope variation might be caused by isotope fractionation in a Rayleigh process when SiO2 precipitated in stem, branches and leaves gradually from plant fluid. In this process the Si isotope fractionation factor between dissolved Si and precipitated Si in bamboo (αpre-sol) is estimated to be 0.9981. However, other factors should be considered to explain the decrease of δ30Si value from roots to stem, including larger ratio of dissolved H4SiO4 to precipitated SiO2 in roots than in stem. There is a positive correlation between the δ30Si values of water-soluble fractions in soils and those of bulk bamboos, indicating that the dissolved silicon in pore water and phytoliths in soil is the direct sources of silicon taken up by bamboo roots. A biochemical silicon isotope fractionation exists in process of silicon uptake by bamboo roots. Its silicon isotope fractionation factor (αbam-wa) is estimated to be 0.9988. Considering the distribution patterns of SiO2 contents and δ30Si values among different bamboo organs, evapotranspiration may be the driving force for an upward flow of a silicon-bearing fluid and silica precipitation. Passive silicon uptake and transportation may be important for bamboo, although the role of active uptake of silicic acid by roots may not be neglected. The samples with relatively high δ30Si values all grew in soils showing high content of organic materials. In contrast, the samples with relatively low δ30Si values all grew in soil showing low content of organic materials. The silicon isotope composition of bamboo may reflect the local soil type and growth conditions. Our study suggests that bamboos may play an important role in global silicon cycle. 相似文献
162.
Hydrogen sulfide (H2S) is known to catalyze thermochemical sulfate reduction (TSR) by hydrocarbons (HC), but the reaction mechanism remains unclear. To understand the mechanism of this catalytic reaction, a series of isothermal gold-tube hydrous pyrolysis experiments were conducted at 330 °C for 24 h under a constant confining pressure of 24.1 MPa. The reactants used were saturated HC (sulfur-free) and CaSO4 in the presence of variable H2S partial pressures at three different pH conditions. The experimental results showed that the in-situ pH of the aqueous solution (herein, in-situ pH refers to the calculated pH of aqueous solution under the experimental conditions) can significantly affect the rate of the TSR reaction. A substantial increase in the TSR reaction rate was recorded with a decrease in the in-situ pH value of the aqueous solution involved. A positive correlation between the rate of TSR and the initial partial pressure of H2S occurred under acidic conditions (at pH ∼3-3.5). However, sulfate reduction at pH ∼5.0 was undetectable even at high initial H2S concentrations. To investigate whether the reaction of H2S(aq) and occurs at pH ∼3, an additional series of isothermal hydrous pyrolysis experiments was conducted with CaSO4 and variable H2S partial pressures in the absence of HC at the same experimental temperature and pressure conditions. CaSO4 reduction was not measurable in the absence of paraffin even with high H2S pressure and acidic conditions. These experimental observations indicate that the formation of organosulfur intermediates from H2S reacting with hydrocarbons may play a significant role in sulfate reduction under our experimental conditions rather than the formation of elemental sulfur from H2S reacting with sulfate as has been suggested previously (Toland W. G. (1960) Oxidation of organic compounds with aqueous sulphate. J. Am. Chem. Soc.82, 1911-1916).Quantification of labile organosulfur compounds (LSC), such as thiols and sulfides, was performed on the products of the reaction of H2S and HC from a series of gold-tube non-isothermal hydrous pyrolysis experiments conducted at about pH 3 from 300 to 370 °C and a 0.1-°C/h heating rate. Incorporation of sulfur into HC resulted in an appreciable amount of thiol and sulfide formation. The rate of LSC formation positively correlated with the initial H2S pressure. Thus, we propose that the LSC produced from H2S reaction with HC are most likely the reactive intermediates for H2S initiation of sulfate reduction. We further propose a three-step reaction scheme of sulfate reduction by HC under reservoir conditions, and discuss the geological implications of our experimental findings with regard to the effect of formation water and oil chemistry, in particular LSC content. 相似文献
163.
含硫化物脉状矿床成矿流体的中阶段 δD亏损:实例与原因 总被引:2,自引:0,他引:2
很多含硫化物脉状金银矿床的成矿过程可以大致分为3个阶段,从早到晚分别以形成黄铁矿-石英组合、多金属硫化物和碳酸盐网脉为标志.所谓中阶段δD亏损,是指在成矿流体δ18O逐渐降低(或升高)时,中阶段δD同时低于早阶段和晚阶段的δD.列举了一些矿床的氢氧同位素研究结果,例证了这种现象的存在;根据中阶段伴随大量硫化物沉淀的事实,认为硫化物沉淀时流体中H2S或HS-的H 被金属离子置换出来,H 加入到流体系统后导致了流体的中阶段δD亏损.对不同温度H2O-H2S体系1000In ot值的概算显示,在200-650℃温度范围,H2S或HS-的δD低于H2O的δD约211‰~478%‰,H2S或HS-中H 的少量释放即可导致流体水δD的显著降低.因此建议,成矿流体从早到晚δ18O逐渐降低,中阶段δD亏损的规律,可以作为含硫化物脉状矿床氢氧同位素演化的概念性模型. 相似文献
164.
165.
166.
A U–Pb sensitive high‐resolution ion microprobe (SHRIMP) age of 654.5 ± 3.8 Ma from an ash bed immediately below the Nantuo Formation in South China provides the lowest age constraint for the Nantuo glaciation, which has been correlated with the global ‘Marinoan’ glaciation. A U–Pb SHRIMP age of 636.3 ± 4.9 Ma from a fallout tuff within the basal layer of the Nantuo Formation, along with the existing age of 635.2 ± 0.6 Ma from its overlying Doushantuo cap carbonate, suggests that the traditionally defined Nantuo Formation may have been deposited in a short time period at the end of the Nantuo glaciation. In combination with available ages globally, the data support a relatively short duration and rapid termination of ‘Marinoan’ glaciations. 相似文献
167.
东北多年冻土区埋地输油管道周围温度场特征非线性分析 总被引:1,自引:0,他引:1
为解决冻土区输油管道周围土壤的温度计算问题,根据考虑相变瞬态温度场的控制微分方程,应用Galerkin法推导出了二维温度场的有限元计算公式.以东北多年冻土区中俄原油管道工程为背景,根据该工程区的冻土条件和气候条件,应用该方法对温热型输油管道土壤温度场进行了计算预报与对比分析.结果表明:对于输送油温为15 ℃、直径为0.914 m以及管顶埋深为2.0 m的管道,在没有铺设保温材料情况下,管顶之上的土壤在管道运行的第1年就达到热平衡状态,同时土壤融化速率在第1年达到最大,随后4a时间里迅速减小,第5年后融化速率变化趋于稳定;管道运行一段时间后,管道周围的融化圈随冷暖季节的变化呈交替式的扩展;在管道运行30 a后,融深>10 m,即管底下的融化层厚>7 m,而在铺设5~8 cm的聚氨酯保温材料后,融深控制在3.08~3.88 m,即管底下融化层厚为0.2~1.0 m.因此,合理使用保温方法能有效防止冻土区管道冻害的发生,同时达到保护冻土环境的目的. 相似文献
168.
中国-俄罗斯原油管道工程(漠河-大庆段)冻土工程地质考察与研究进展 总被引:4,自引:2,他引:2
李国玉 金会军 盛煜 张建明 俞祁浩 齐吉琳 温智 吕兰芝 童长江 郭东信 王绍令 魏智 杨思忠 吉延俊 于少鹏 何瑞霞 常晓丽 郝加前 陈友昌 吴伟 翟镇远 赵意民 《冰川冻土》2008,30(1):170-175
在2005-2007年期间,先后3次对中国-俄罗斯原油管道漠河-大庆段沿线的冻土工程地质条件等进行科学考察,开展了冻土工程地质条件及其在气候变化和人类活动作用下的评价和预测研究.考察研究结果表明:管道沿线多年冻土在各类融区、季节冻土和水系等分隔作用下呈片状或岛状分布,沿线岛状、稀疏岛状及零星岛状占多年冻土区段的40%左右;管道沿线多年冻土随着气候的转暖和人类活动的影响不断退化.地形地貌单元、植被分布、地表水分条件的变化等局部因素对多年冻土的分布和地下冰的赋存产生重要的影响,管道沿线大约分布有50 km左右的沼泽湿地,其表层为腐殖质土及泥炭层,泥炭层下面分布着含土冰层或地下冰,是管道沿线最差的冻土工程地质地段;由于中俄原油管道沿线水系发育多,冻胀丘、冰椎和冰幔等不良冻土现象广泛分布.科学考察的成果为管道沿线冻土工程地质条件评价和预测、管道的稳定性影响分析以及后期的长期检测系统设置等研究奠定坚实的基础,进一步为即将开工的中俄原油管道漠河-大庆段工程的设计、施工提供科学依据. 相似文献
169.
泸州古隆起对贵州赤水地区早、中三叠世沉积环境和相带展布的控制 总被引:6,自引:0,他引:6
地质历史中,区域大地构造和区域古地貌单元的不同特征是控制沉积相带展布及发育的主要因素之一。东吴运动形成的泸州古隆起是影响本区沉积相带展布的重要因素。早、中三叠世时,泸州古隆起的高部位向南延伸到太和场以南,宝元以北一带。宝元、龙爪等构造处于泸州古隆起东南部斜坡上,而宝元构造处于古隆起东南部斜坡上部,龙爪构造处于古隆起东南部斜坡中部。此古地貌格局,与区域海平面升降一起,控制了早三叠世沉积相带展布和地层厚度。在古地貌高的隆起区域,由于水体开阔、水动力条件相对较强,沉积了有利于形成储集体的滩相沉积物(生屑滩、砂屑滩、鲕粒滩等)。从泸州古隆起的高部位向古隆起的斜坡区,地层厚度逐渐增大,沉积物向粒度变细、颜色加深的特征相变。 相似文献
170.
青藏高原西部赛利普中新世火山岩源区:地球化学及Sr-Nd同位素制约 总被引:11,自引:6,他引:5
青藏高原拉萨地块西部赛利普地区新生代火山岩依据主量元素可划分为超钾质、钾质和钙碱性系列,主要的岩石类型为粗面安山岩、粗面岩,一个超钾质岩石的40Ar-39Ar年龄为17.58Ma,指示出火山活动为中新世.超钾质、钾质和钙碱性火山岩都显示出富集LREE及LILE(Th、U)、亏损HFSE(Nb、Ta、Ti)的特征.超钾质火山岩具有较高的K2O(6.31%~8.55%)、MgO(6.75%~8.96%)、Cr(270.7×10-6~460.4×10-6)、Ni(142.3×10-6~233.9×10-6)含量,较高的(87Sr/86Sr)i(0.71883~0.72732)和较低的εNd(-14.78~-15.37),指示可能起源于一个前期亏损并经后期俯冲作用改造的富钾的方辉橄榄岩富集地幔源区.钾质火山岩具有比超钾质火山岩低的K2O、MgO、Cr、Ni含量以及高的Ba、Sr含量,初始87Sr/86Sr为0.71553~0.71628,初始143Nd/144Nd为0.51197~0.51198,在空间上与超钾质火山岩共生,可能是前者母岩浆的演化产物.钙碱性火山岩具有较高的Sr(881.7×10-6~1309.2×10-6)、Sr/Y比值(50~108)和较低的Y(12.05×10-6~18.02×10-6),明显亏损重稀土Yb(0.93×10-6~1.30×10-6),类似于典型的埃达克质岩成分特征但相对高钾,并具有相对低的(87Sr/86Sr);(0.70928~0.71374)以及高的εNd(-7.90~-10.91),指示起源于富钾增厚下地壳物质的部分熔融.区域上拉萨地块超钾质岩、钾质岩与N-S向地堑系在空间上共存、时间上相吻合,由此本文认为拉萨地块中新世钾质.超钾质岩和南北向地堑系的形成可能与中新世早期北向俯冲的印度大陆岩石圈断离有关. 相似文献