全文获取类型
收费全文 | 1649篇 |
免费 | 233篇 |
国内免费 | 392篇 |
专业分类
测绘学 | 147篇 |
大气科学 | 259篇 |
地球物理 | 546篇 |
地质学 | 789篇 |
海洋学 | 231篇 |
天文学 | 82篇 |
综合类 | 69篇 |
自然地理 | 151篇 |
出版年
2024年 | 11篇 |
2023年 | 25篇 |
2022年 | 64篇 |
2021年 | 62篇 |
2020年 | 74篇 |
2019年 | 89篇 |
2018年 | 64篇 |
2017年 | 63篇 |
2016年 | 88篇 |
2015年 | 73篇 |
2014年 | 96篇 |
2013年 | 138篇 |
2012年 | 83篇 |
2011年 | 129篇 |
2010年 | 97篇 |
2009年 | 115篇 |
2008年 | 102篇 |
2007年 | 118篇 |
2006年 | 135篇 |
2005年 | 87篇 |
2004年 | 77篇 |
2003年 | 69篇 |
2002年 | 56篇 |
2001年 | 57篇 |
2000年 | 51篇 |
1999年 | 41篇 |
1998年 | 39篇 |
1997年 | 22篇 |
1996年 | 30篇 |
1995年 | 25篇 |
1994年 | 19篇 |
1993年 | 21篇 |
1992年 | 19篇 |
1991年 | 5篇 |
1990年 | 8篇 |
1989年 | 1篇 |
1988年 | 5篇 |
1987年 | 3篇 |
1986年 | 4篇 |
1985年 | 2篇 |
1984年 | 1篇 |
1982年 | 2篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1973年 | 1篇 |
1954年 | 1篇 |
排序方式: 共有2274条查询结果,搜索用时 15 毫秒
101.
Household consumption represents an important proportion of all energy consumption,and it is an important source of CO2 emission. But household consumption and carbon emissions are often overlooked in climate change policies and measures. Through literature review, the research status of household consumption and carbon emissions were reviewed. On this basis, the main aspects and directions of the research are summarized and the main research of household carbon emissions should focus on three aspects in the future: ①The impact of income, consumption levels and other factors on household carbon emission; ②The relationship between direct and indirect carbon emissions of household carbon emission; ③The structure and source of household carbon emission. In future research, there are four issues which need in-depth study: ①Index and models study of household carbon emissions;②Impact of demographic change on household carbon emissions; ③The path of how to achieve sustainable and green urban lifestyle;④The relevant policy research of household carbon emissions. 相似文献
102.
Celestite formation, bacterial sulphate reduction and carbonate cementation of Eocene reefs and basinal sediments (Igualada, NE Spain) 总被引:5,自引:0,他引:5
Conxita Taberner James D. Marshall† James P. Hendry‡ Catherine Pierre§ & M. F. Thirlwall¶ 《Sedimentology》2002,49(1):171-190
Petrographic and geochemical studies of an Upper Eocene reef and associated basinal sediments from the mixed carbonate–siliciclastic fill of the south‐eastern Pyrenean foreland basin near Igualada (NE Spain) provide new insights into the evolution of subsurface hydrology during the restriction of a marine basin. The reef deposits are located on delta‐lobe sandstones and prodelta marls, which are overlain by hypersaline carbonates and Upper Eocene evaporites. Authigenic celestite (SrSO4) is an important component in the observed diagenetic sequences. Celestite is a significant palaeohydrological indicator because its low solubility constrains transportation of Sr2+ and SO42? in the same diagenetic fluid. Stable isotopic analyses of carbonates in the reef indicate that meteoric recharge was responsible for aragonite stabilization and calcite cementation. Sulphur and oxygen isotope geochemistry of the celestite demonstrates that it formed from residual sulphate after bacterial sulphate reduction, but also requires that there was a prior episode of sulphate recycling. Meteoric water reaching the reef and basinal areas was most probably charged with SO42? from the dissolution of younger Upper Eocene marine evaporites. This sulphate, combined with organic matter present in the sediments, fuelled bacterial sulphate reduction in the meteoric palaeoaquifer. Strontium for celestite precipitation was partly derived in situ from dissolution of aragonite corals in the reef and basinal counterparts. However, 87Sr/86Sr data also suggest that Sr2+ was partly derived from dissolution of overlying evaporites. Mixing of these two fluids promoted celestite formation. The carbonate stable isotopic data suggest that the local meteoric water was enriched in 18O compared with that responsible for stabilization of other reefs along the basin margin. Furthermore, meteoric recharge at Igualada post‐dated evaporite deposition in the basin, whereas other parts of the same reef complex were stabilized before evaporite formation. This discrepancy resulted from the spatial distribution of continental siliciclastic units that acted as groundwater conduits. 相似文献
103.
长输油气管道经过黄土冲沟边坡时常常采用斜井穿越的方式,采用数值强度折减法与实际地形建模结合的方法,以陕西千阳黄土冲沟边坡为例,通过对黄土力学参数的不断折减,以收敛性准则作为边坡是否产生滑动的破坏判据,根据边坡滑动时的位移等值线图确定了边坡潜在滑动面的形状及位置,确定了管线穿越斜井的初始安全设计参数;基于初步设计参数研究了管线斜井开挖过程中井周土体的位移变化规律,并对斜井开挖后黄土冲沟边坡的稳定性安全系数进行了进一步分析计算。分析结果表明,所给出的管线穿越斜井设计参数的确定方法,能在设计阶段有效避开冲沟边坡潜在滑动区,基于这种设计参数使得管道斜井施工对边坡稳定性影响很小,边坡安全系数由1.162变为1.156,变化不大。根据计算结果,对斜井支护区域也提出了合理的建议。 相似文献
105.
基于场变量的边坡稳定分析有限元强度折减法? 总被引:1,自引:0,他引:1
有限元强度折减法在实施过程中往往要根据不同的折减系数手工修改输入文件,并不断进行试算,过程较繁琐。为了简化计算过程,提高计算效率,在有限元强度折减法的基础上,结合ABAQUS提供的场变量,提出一种适用于有限元强度折减计算的新方法--基于场变量的有限元强度折减法。通过在ABAQUS中设置岩土体黏聚力与内摩擦角为场变量的函数,场变量为增量步时间t的函数,从而通过控制增量步时间t实现黏聚力与内摩擦角的折减,通过一次计算即可求得边坡的安全系数,无需手工修改折减系数反复试算。结合有关文献对该方法用于边坡稳定分析的可行性进行了验证,并与二分法确定安全系数的计算效率进行了比较。结果表明:该方法求得的安全系数是有效可靠的,用于边坡稳定性的计算是可行的,简化了有限元强度折减法的计算过程,提高了计算效率。 相似文献
106.
《城镇污水处理厂污泥处理处置技术规范》[1]执行前,市政污泥往往直接倾倒于填埋场形成污泥库,导致垃圾设计库容显著降低。为恢复填埋场库容,许多填埋场面临污泥库的原位加固处理。通过2组模型试验,探讨真空预压处理污泥的可行性。试验结果表明,真空预压后污泥含水率显著降低,强度提高至2~4 kPa;污泥排水固结系数随预压过程发展表现出非线性;排水板周围污泥含水率和渗透系数降低明显,阻碍离排水板较远处污泥排水固结,因此减少排水板间距可显著提高污泥处理效果;真空预压过程中污泥中孔压变化规律与常规淤泥质土有明显区别,特别是远离排水板的位置孔压消散幅度小,表明污泥中孔压消散规律不符合传统的太沙基固结理论;污泥真空预压过程中,间歇式通正气压会在处理初期阶段加快排水速率,但整体改善作用不明显;真空预压可作为污泥减量化的一种途径,如要满足后续堆载垃圾的要求,还需配合其他原位处理方法进一步提高强度。 相似文献
107.
汶川地震造成大量的边坡支挡结构的破坏,边坡抗震设计必须进行新的考虑。提出基于性能设计的原则为边坡抗震设计方法,即边坡支挡结构抗震设计应该按照3级设防的要求规定如下:遭遇多遇地震时候,边坡处于稳定状态,要求稳定系数达到1.2; 遭遇设计地震时候,边坡处于基本稳定状态,要求稳定系数达到1.15; 遭遇罕遇地震时,边坡处于欠稳定状态,要求稳定系数达到1.05。采用上述抗震设计方法,结合具体算例,采用强度折减动力分析法进行了算例边坡抗震设计,结果表明基于性能设计的方法,既满足抗震设计总的原则,又具有很强的可操作性,对边坡支挡结构抗震设计具有重要意义。 相似文献
108.
Lallan Prasad Gupta Hodaka Kawahata Mio Ltakeuchi Hidekazu Ohta Yoshiro Ono 《Resource Geology》2006,56(2):191-196
Abstract. Oxidation and reduction processes can influence extent of leaching of elements from solid waste. Three samples of municipal solid waste combustion fly ash were subjected to oxidizing and reducing conditions in order to evaluate leaching of elements in the Milli-Q water and fly ash (liquid to solid ratio, 100) mixtures. Although the oxidizing and reducing conditions were applied for 6 hours only, elements like Cs, Li, Mg, Sb, Tl and V leached more under oxidizing condition than under reducing condition in the case of all three ash samples. Cadmium, Pb and Zn leached more from all samples under reducing condition than under oxidizing condition. Leaching of other elements like Al, Ba, Cr, Cu, Ni and Rb was inconsistent with oxidizing or reducing conditions and varied from sample to sample, suggesting that factors other than redox may be more important in controlling leaching of these elements. Strong acid neutralization capacity of the fly ash samples let the pH vary within a narrow range, and thus severely limited the extent of leaching during the course of the experiment. Lead and Zn were the most sensitive while K and Na were the least sensitive to changes in redox conditions. 相似文献
109.
介绍了时间域拉东正反变换的基本原理及该项技术在地震数据处理中的应用.以Ng和Perz的算法为基础,以开发地震勘探处理与解释系统为实例,解决了实验中遇到的拉东正变换时收敛精度、反变换数据无损还原和截断信号引起的能量扩散、低信噪比情况下的滤波等问题,进一步研究了改进算法在其他地形下应用问题. 相似文献
110.
Guangyou?ZhuEmail author Shuichang?Zhang Yingbo?Liang Jinxing?Dai Jian?Li 《中国科学D辑(英文版)》2005,48(11):1960-1971
The northeastern area of Sichuan Basin, southwestern China, is the area with the maximal reserve of natural gas containing
higher hydrogen sulphide (H2S) that has been found among the petroliferous basins of China, with the proven and controlled gas reserve of more than 200
billion cubic meters. These gas pools, with higher H2S contents averaging 9%, some 17%, are mainly distributed on structural belts of Dukouhe, Tieshanpo, Luojiazhai, Puguang,
etc., while the oolitic-shoal dolomite of the Triassic Feixianguan Fm. (T1f) is the reservoir. Although many scholars regard the plentiful accumulation of H2S within the deep carbonate reservoir as the result of Thermochemical Sulfate Reduction (TSR), however, the process of TSR
as well as its residual geological and geochemical evidence is still not quite clear. Based on the carbon isotopic analysis
of carbonate strata and secondary calcite, etc., together with the analysis of sulfur isotopes within H2S, sulphur, gypsum, iron pyrites, etc., as well as other aspects including the natural gas composition, carbon isotopes of
hydrocarbons reservoir petrology, etc., it has been proved that the above natural gas is a product of TSR. The H2S, sulphur and calcite result from the participation of TSR reactions by hydrocarbon gas. During the process for hydrocarbons
being consumed due to TSR, the carbons within the hydrocarbon gas participate in the reactions and finally are transferred
into the secondary calcite, and become the carbon source of secondary calcite, consequently causing the carbon isotopes of
the secondary calcite to be lower (−18.2‰). As for both the intermediate product of TSR, i.e. sulfur, and its final products,
i.e. H2S and iron pyrites, their sulfur elements are all sourced from the sulfate within the Feixianguan Fm. During the fractional
processes of sulfur isotopes, the bond energy leads to the 32S being released firstly, and the earlier it is released, the lower δ 34S values for the generated sulphide (H2S) or sulfur will be. However, for the anhydrite that participates in reactions, the higher the reaction degree, the more
32S is released, while the less 32S remains and the more δ 34S is increased. The testing results have proved the process of the dynamic fractionation of sulfur isotopes. 相似文献