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21.
M.D. Morrison 《Planetary and Space Science》1985,33(1):135-139
Laboratory measurements of the Å (3s' 3D° → 2p41D, 3s' 3D° → 2p43P) branching ratio have been made with a value of 1.5 × 10t-4 indicated. This value makes the branching transition at 1173 Å an order of magnitude stronger than the branch at 7990 Å (3s' 3D° → 3p 3P). The 1173 Å branching loss is still too weak a loss process for multiply scattered 989 Å photons to resolve the 989 Å intensity problem in the dayglow. 相似文献
22.
R. J. DELMAS P. WAGNON K. GOTO-AZUMA K. KAMIYAMA O. WATANABE 《Tellus. Series B, Chemical and physical meteorology》2003,55(1):71-79
We have examined several MSA (methanesulfonic acid) records from the upper 200 m of the Antarctic ice sheet and in particular the new Dome F profile. At all the four sites studied, concentration profiles exhibit similar patterns as a function of depth. They suggest that snow metamorphism and solid phase migration are responsible for a marked release of gaseous MSA to interstitial firn air as well as probably to the free atmosphere, in particular at extremely low accumulation sites. Snow acidity can also modify MSA concentration. It is proposed that, below the upper few metres where the communication with the free atmosphere is possible, gaseous MSA may remain in the firn layers and be entrapped later in air bubbles at pore close-off, i.e. when firn is transformed into ice. Chemical measurements on the firn core do not take into account the MSA released to the gaseous phase, but this fraction is measurable in ice samples. In spite of these alterations occurring in the firn layers, relative changes of the atmospheric MSA concentration in the past are probably still there deep within the Antarctic ice sheet. However, for glacial periods, different processes have to be considered in relation to modified aerosol properties. 相似文献
23.
A discrete element modelling of bonded granulates and investigation on the bond effect on their behaviour are very important to geomechanics. This paper presents a two‐dimensional (2‐D) discrete element theory for bonded granulates with bond rolling resistance and provides a numerical investigation into the effect of bond rolling resistance on the yielding of bonded granulates. The model consists of mechanical contact models and equations governing the motion of bonded particles. The key point of the theory is that the assumption in the original bond contact model previously proposed by the authors (55th CSCE‐ASCE Conference, Hamilton, Ont., Canada, 2002; 313–320; J. Eng. Mech. (ASCE) 2005; 131 (11):1209–1213) that bonded particles are in contact at discrete points, is here replaced by a more reliable assumption that bonded particles are in contact over a width. By making the idealization that the bond contact width is continuously distributed with the normal/tangential basic elements (BE) (each BE is composed of spring, dashpot, bond, slider or divider), we establish a bond rolling contact model together with bond normal/tangential contact models, and also relate the governing equations to local equilibrium. Only one physical parameter β needs to be introduced in the theory in comparison to the original bond discrete element model. The model has been implemented into a 2‐D distinct element method code, NS2D. Using the NS2D, a total of 86 1‐D, constant stress ratio, and biaxial compressions tests have been carried out on the bonded granular samples of different densities, bonding strengths and rolling resistances. The numerical results show that: (i) the new theory predicts a larger internal friction angle, a larger yielding stress, more brittle behaviour and larger final broken contact ratio than the original bond model; (ii) the yielding stress increases nonlinearly with the increasing value of β, and (iii) the first‐yield curve (initiation of bond breakage), which define a zone of none bond breakage and which shape and size are affected by the material density, is amplified by the bond rolling resistance in analogous to that predicted by the original bond model. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
24.
The Electron Energy Spectrum from Large Solar Flares 总被引:2,自引:0,他引:2
G. M. Simnett 《Solar physics》2006,237(2):383-395
We report on the differential electron spectrum for intense transient events seen at one AU by the EPAM instrument on the
Advanced Composition Explorer (ACE) spacecraft. Over an observing period from September 1997 to September 2005, there were 45 major events that could be
reliably identified with a source flare on the Sun. In the ∼40 – 300 keV energy range, the electron spectral index was between
one and three for all but two of the events. Twenty-five of the events were associated with Geostationary Operational Environmental
Satellites (GOES) X-ray class X flares. We compare this result with the spectral index measured from electron pulse events,
lasting approx. one hour or less, where the spectral index is typically much softer than three. This suggests that the measured
spectral index of near-relativistic electrons at one AU may be a reliable indicator of the source. We also examine the likelihood
that fast coronal mass ejections (CMEs) are responsible in themselves for accelerating near-relativistic electrons and conclude
that they do not. 相似文献
25.
A new approach to constraining seawater δ34S and sulphate concentration using francolite‐bound sulphate reveals an abrupt increase in δ34S to +50‰ around the Early–Middle Cambrian boundary. Such high δ34S values are best explained by increased rates of pyrite burial due to ocean anoxia coupled with an increased sensitivity of the ocean sulphate reservoir to perturbations due to low sulphate concentrations of 500–700 μgL?1. We argue that the spread of anoxic waters at this time was partly the result of greenhouse warming related to the eruption of the Kalkarindji Large Igneous Province of northern Australia and that it triggered the collapse of early metazoan reef ecosystems during the latest Early Cambrian. Mass extinctions of the last 260 Myr have all coincided with enhanced volcanic activity, while several are also associated with positive shifts in seawater δ34S. Extending this correlation back in time further implicates volcanically induced climate change as a major determining factor in biosphere evolution. Terra Nova, 18, 257–263, 2006 相似文献
26.
Florent Deleflie Gilles Métris Pierre Exertier 《Celestial Mechanics and Dynamical Astronomy》2006,94(1):83-104
This paper studies the long period variations of the eccentricity vector of the orbit of an artificial satellite, under the
influence of the gravity field of a central body. We use modified orbital elements which are non-singular at zero eccentricity.
We expand the long periodic part of the corresponding Lagrange equations as power series of the eccentricity. The coefficients
characterizing the differential system depend on the zonal coefficients of the geopotential, and on initial semi-major axis,
inclination, and eccentricity. The differential equations for the components of the eccentricity vector are then integrated
analytically, with a definition of the period of the perigee based on the notion of “free eccentricity”, and which is also
valid for circular orbits. The analytical solution is compared to a numerical integration. This study is a generalization
of (Cook, Planet. Space Sci., 14, 1966): first, the coefficients involved in the differential equations depend on all zonal coefficients (and not only on
the very first ones); second, our method applies to nearly circular orbits as well as to not too eccentric orbits. Except
for the critical inclination, our solution is valid for all kinds of long period motions of the perigee, i.e., circulations
or librations around an equilibrium point. 相似文献
27.
28.
The study of the chemical stability of vitreous material in aqueous media is well‐established. There has to date been little consideration of the implications of variations in the chemical durability of tephra in Quaternary tephrochronology. Chemical alteration can take the form of cationic leaching from the matrix, or complete destruction of the silica network, either of which could constrain the ability to chemically identify distal tephra. Here we apply established models of vitreous durability to the published chemical analyses of a large number of Icelandic tephras in order to predict their relative durabilities under equivalent conditions. This suggests that some important tephras have relatively poor chemical stability, and that rhyolitic tephras are, in general, more stable than basaltic. We conclude that tephras should be expected to show predictable differential chemical stability in the post‐depositional environment. Copyright © 2003 John Wiley & Sons, Ltd. 相似文献
29.
The most general accurate solutions for the Buchdhal fluid sphere were obtained and matched with the Schwarzchild's exterior
solution at the pressure free interface. Various parameters of the solutions were so adjusted that the energy density, pressure
and temperature were positive and decreasing away from the centre, and the velocity of sound was less than unity throughout
the spheroid model. Using this procedure, the maximum mass of the fluid sphere with a surface density of2 × 1014gm cm-3 was determined to be 3.82MΘ and 4.57 MΘ for strong and weak energy conditions respectively. PACS number: 0402, 0402J, 0440D,
95301
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
30.
Summary ?A single-crystal X-ray investigation was performed on crystals of P21/c natural pigeonite with varying Ca and Fe* ( = Fe2+ + Mn2+) contents, in order to verify the effect of microtextural disorder on structure refinements and to constrain the crystal
chemistry of pigeonite. Antiphase domains and exsolution lamellae affect differently the refinement results. In a crystal
free of exsolution the structure obtained after refinement with all reflections is an average of that of the antiphase domains
and of their boundaries, whereas in an exsolved crystal it represents only the structure of the prevailing pigeonite lamellae.
The refinement using only h + k odd reflections seems to give the structure of the Ca-free pigeonite characteristic of the antiphase domains rather than
that of Ca-rich domain walls. The ratio of the scale factors in refinements with all reflections and with only h + k odd reflections allows the ratios of the exsolved augite and pigeonite phases to be estimated.
The crystal chemistry of the investigated samples follows the trends outlined by data on Ca-free and Fe-free synthetic samples.
In particular, it is shown that Ca and Fe* substitution for Mg induce similar changes in the average structure, i.e. both induce an expansion in the M1 polyhedron and
decrease the difference between the M2–O3 distances.
Received October 18, 2001; revised version accepted February 15, 2002 相似文献