全文获取类型
收费全文 | 3787篇 |
免费 | 529篇 |
国内免费 | 569篇 |
专业分类
测绘学 | 265篇 |
大气科学 | 490篇 |
地球物理 | 1221篇 |
地质学 | 1638篇 |
海洋学 | 640篇 |
天文学 | 150篇 |
综合类 | 170篇 |
自然地理 | 311篇 |
出版年
2024年 | 20篇 |
2023年 | 58篇 |
2022年 | 78篇 |
2021年 | 114篇 |
2020年 | 219篇 |
2019年 | 168篇 |
2018年 | 172篇 |
2017年 | 253篇 |
2016年 | 190篇 |
2015年 | 214篇 |
2014年 | 327篇 |
2013年 | 497篇 |
2012年 | 339篇 |
2011年 | 135篇 |
2010年 | 137篇 |
2009年 | 138篇 |
2008年 | 135篇 |
2007年 | 205篇 |
2006年 | 169篇 |
2005年 | 141篇 |
2004年 | 140篇 |
2003年 | 109篇 |
2002年 | 121篇 |
2001年 | 88篇 |
2000年 | 71篇 |
1999年 | 94篇 |
1998年 | 79篇 |
1997年 | 73篇 |
1996年 | 73篇 |
1995年 | 55篇 |
1994年 | 62篇 |
1993年 | 45篇 |
1992年 | 45篇 |
1991年 | 36篇 |
1990年 | 17篇 |
1989年 | 25篇 |
1988年 | 9篇 |
1987年 | 13篇 |
1986年 | 5篇 |
1985年 | 2篇 |
1984年 | 2篇 |
1983年 | 5篇 |
1982年 | 2篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1978年 | 1篇 |
1954年 | 1篇 |
排序方式: 共有4885条查询结果,搜索用时 109 毫秒
991.
992.
993.
本文详细回顾了克利斯托费尔方程(Christoffel)的推导.在此基础上,提炼出时空域和频率域克利斯托费尔方程,前者可作正演计算介质的相速度,后者可计算介质的群速度.并计算了横观各向同性介质的相速度和群速度.最后对无损耗各向异性介质的相速度和群速度的关系进行了简单讨论. 相似文献
994.
本文发展了积分方程法用于层状介质中三维不均匀体的大地电磁模拟算法(简称MT).分为二个步骤:第一步,异常体用等效的散射电流代替,通过层状介质中的格林函数,建立以散射电流为未知参数的积分方程;第二步,把求得的散射电流乘上相应的格林函数,即得地面上的二次电磁场,由此而计算出各种MT响应. 文中采用了数值滤波与插值、群变换以及格林矩阵带状化三个方面的数值处理方法,提高了计算效率.通过与已发表的三维MT计算结果对比及格林函数互易性检验,表明了该算法的正确性.在此基础上,进行了数值模拟,初步讨论了三维MT曲线的畸变特点. 相似文献
995.
In order to consider the effect of anisotropy on the periods of the oscillations of the Earth, the problem of toroidal oscillations
of a transradially isotropic elastic sphere is considered. At each point, the medium is assumed to be transversely isotropic
about the radius through the point. The roots of the frequency equation are obtained for different values of the anisotropy
parameter α. It is found that, for large order oscillations, the percentage change in the frequency of the toroidal oscillations
on account of the anisotropy is nearly equal to |α-1| × 100. 相似文献
996.
Here we describe the first sauropod skeletal remains from the Italian peninsula that also represent the earliest record of titanosaurs in Southern Europe. Scattered bones, including an almost complete anterior caudal vertebra, were found in Cretaceous (Aptian–Albian) marine deposits, some 50 km East of Rome. The vertebra shows a bizarre and perhaps unique orientation of the zygapophyseal articular facets that renders their interpretation problematic. Phylogenetic retrofitting tests support the placement of the Italian titanosaur among basal lithostrotians. Palaeobiogeographic analysis based on the resulting phyletic relationships suggests an Afro-Eurasian route for the ancestors of the Italian titanosaur, a scenario compatible with the palaeogeographic evolution of the Italian microplates during the Cretaceous. Together with previously recorded titanosaurian-like ichnites from a Cenomanian locality in Latium, this new find suggests a quite long emersion for the Apenninic carbonate platform. We suggest that the Italian titanosaur was member of a population that crossed the western Tethys Sea through a “filtering bridge” composed of a chain of ephemeral islands and peninsulae, known as Periadriatic (Adria) carbonate platforms, that connected sporadically Africa and Europe since the Early Cretaceous. 相似文献
997.
This paper is concerned with the vibration isolation efficiency analysis of total or partially buried thin walled wave barriers in poroelastic soils. A two-dimensional time harmonic model that treats soils and structures in a direct way by combining appropriately the conventional Boundary Element Method (BEM), the Dual BEM (DBEM) and the Finite Element Method (FEM) is developed to this aim. The wave barriers are impinged by Rayleigh waves obtained from Biot’s poroelasticity equations assuming a permeable free-surface. The suitability of the proposed model is justified by comparison with available previous results. The vibration isolation efficiency of three kinds of wave barriers (open trench, simple wall, open trench-wall) in poroelastic soils is studied by varying their geometry, the soil properties and the frequency. It is found that the efficiency of these wave barriers behaves similarly to these in elastic soils, except for high porosities and small dissipation coefficients. The efficiency of open trench-wall barriers can be evaluated neglecting their walls if they are typical sheet piles. This does not happen with walls of bigger cross-sections, leading in general to efficiency losses. Likewise, increasing the burial depth to trench depth ratio has a negative impact on the efficiency. 相似文献
998.
999.
This paper presents numerical simulations of Cone Penetration Test (CPT) in water-saturated soft soils taking into account pore pressure dissipation during installation. Besides modelling interaction between soil skeleton and pore fluid, the problem involves large soil deformations in the vicinity of the penetrometer, soil–structure interaction, and complex non-linear response of soil. This makes such simulations challenging. Depending on the soil’s permeability and compressibility, undrained, partially drained or drained conditions might occur. Partially drained conditions are commonly encountered in soils such as silts and sand–clay mixtures. However, this is often neglected in CPT interpretation, which may lead to inaccurate estimates of soil properties. This paper aims at improving the understanding of the penetration process in different drainage conditions through advanced numerical analyses. A two-phase Material Point Method is applied to simulate large soil deformations and generation and dissipation of excess pore pressures during penetration. The constitutive behaviour of soil is modelled with the Modified Cam Clay model. Numerical results are compared with experimental data showing good agreement. 相似文献
1000.
The Hell Creek Formation and its contribution to the Cretaceous–Paleogene extinction: A short primer
Although it represents but one geographic data point, the uppermost Maastrichtian Hell Creek Formation (HCF), exposed in the upper Great Plains of the North American craton, remains the most studied source for understanding the final ∼1.5 Myr of the Mesozoic Era in the terrestrial realm. Because it lies conformably below the earliest Paleocene Fort Union Formation, and together these two units preserve a rich fauna and flora, much of what is understood about the terrestrial Cretaceous–Paleogene (K–Pg) boundary comes from this sequence.The HCF has been reconstructed as an expansive, fluvially drained, low coastal plain, built out, to the west, against the Laramide Orogen, and to the east, against the ultimate transgression (Cannonball) of the Western Interior Sea. Its meandering rivers and moist soils supported a multi-tiered angiosperm-dominated flora and rich insect and vertebrate faunas, including dinosaurs, crocodilians, squamates, turtles, and mammals. A dramatic facies change representing the initiation of catastrophic flooding is preserved, within available levels precision, at the K–Pg boundary.High-precision stratigraphy has proven difficult in this lenticular fluvial system. Where present, the boundary can be recognized by the bipartite boundary claystone; otherwise, palynostratigraphy has proven a powerful tool. Numerical dates have been successfully obtained from in tonsteins at the boundary and above, in the Fort Union; however, these have proven elusive below the boundary within the HCF. The K–Pg boundary in this region is dated at 66.043 Ma (Renne et al., 2013). Magnetostratigraphic studies have been carried out in the HCF; although all but one have lacked numerical dates, these have been used for correlations of widespread, disjunct exposures and for the estimation of sedimentation rates.The palynoflora is largely homogenous through the HCF; at the K–Pg boundary, it shows an abrupt ∼30% extinction. This makes it a powerful tool for identification of the K–Pg boundary, although because the boundary is identified on absence of Cretaceous taxa rather than presence of earliest Paleocene taxa, several competing methods have been applied to identifying the K–Pg boundary using pollen.The macroflora, consisting largely of leaves, consists of three successive floras, showing increasing diversity through the HCF. The ultimate of these three floras undergoes an abrupt 57% extinction; taken as a whole, however, the macroflora undergoes a 78% extinction at the K–Pg boundary.The best data available for dinosaurs – including archaic Aves – show an abrupt extinction. By contrast, salamanders and other lissamphibians, as well as chelonians, cross the boundary virtually without perturbation. Squamates appear to have suffered significant extinctions at the K–Pg boundary, as did euselachians (elasmobranchs) and insects. Mammals suffered a 75% extinction; however, some of this figure cannot be shown to have occurred in less than the last 500 kyr of the Cretaceous, and thus has been potentially attributable to causes other than a bolide impact. Taken together, the survivorship patterns are concordant with the catastrophic inception of ubiquitous flooding characterizing the K–Pg boundary.While the key K–Pg boundary question in the HCF was once the rate of the biotic extinction, it has moved to the distinction between single-cause scenarios, with the Chicxulub bolide as agent of extinction, and multi-cause scenarios, uniting habitat partitioning, Deccan flood-basalt volcanism, climate change, competition, and bolide impact. Not every potential environmental perturbation need be a mechanism for the extinction: parsimony and the data continue to be concordant with a bolide impact as the single agent of the terrestrial K–Pg mass extinction. 相似文献