首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   2425篇
  免费   162篇
  国内免费   19篇
测绘学   102篇
大气科学   272篇
地球物理   724篇
地质学   936篇
海洋学   175篇
天文学   255篇
综合类   24篇
自然地理   118篇
  2022年   21篇
  2021年   69篇
  2020年   51篇
  2019年   48篇
  2018年   110篇
  2017年   106篇
  2016年   152篇
  2015年   126篇
  2014年   146篇
  2013年   225篇
  2012年   175篇
  2011年   170篇
  2010年   138篇
  2009年   116篇
  2008年   104篇
  2007年   80篇
  2006年   103篇
  2005年   57篇
  2004年   50篇
  2003年   55篇
  2002年   57篇
  2001年   40篇
  2000年   25篇
  1999年   19篇
  1998年   24篇
  1997年   21篇
  1996年   15篇
  1995年   22篇
  1994年   15篇
  1993年   12篇
  1992年   10篇
  1991年   25篇
  1990年   11篇
  1989年   12篇
  1988年   7篇
  1987年   10篇
  1986年   8篇
  1985年   10篇
  1984年   17篇
  1983年   13篇
  1982年   11篇
  1981年   8篇
  1980年   6篇
  1979年   14篇
  1977年   5篇
  1976年   6篇
  1975年   9篇
  1974年   7篇
  1973年   11篇
  1969年   8篇
排序方式: 共有2606条查询结果,搜索用时 15 毫秒
21.
The present paper deals with the specification of bed erosion flux that accounts for the effects of sediment-induced stratification in the water column. Owing to difficulties in measuring the bed shear stress b and the erosive shear strength s, we suggest a series of methods that combine laboratory and numerical experiments. A simplified turbulent transport model that includes these effects helps to quantify b and s. Focusing on soft stratified beds, the present study considers erosion rate formulas of the form =f exp {[Tb-Ts]} where is a model constant (=1 for Gularte's (1978) formula and =1/2 for Parchure's (1984) formula). First, the bed erosive strength profile s(Z) is adjusted by forcing the turbulent transport model with measured erosion rates. Second, three procedures are suggested to determine the erosion rate formula coefficients f and : a global procedure and two different layer-by-layer procedures. Each procedure is applied to an erosion experiment conducted in a rotating annular flume by Villaret and Paulic (1986). The use of the layer-by-layer procedure based on a least squares fitting technique provides a closer fit than the global procedure. The present study points out the complementarity of experimental and numerical approaches and also suggests possible improvements in laboratory test procedures.  相似文献   
22.
Dioctahedral smectite is present as a retrograde alteration product of chlorite in Permian-Triassic red slates of the Malaguide Complex in Sierra de Espuña (Betic Cordillera). Mineral assemblages and textures, illite crystallinity indices, and fluid inclusion data indicate sub-greenschist facies conditions that reached at least 180°C in the higher-grade tectonic unit of the Malaguide Complex, preceding formation of smectite. Smectite, having K as the dominant interlayer cation, occurs ubiquitously intercalated with trioctahedral chlorite as thin packets of layers and as individual layers that commonly change to chlorite along layers. Although some chlorite is typically homogeneous and trioctahedral, much chlorite shows signs of alteration and has compositions corresponding to different degrees of smectite contaimination. The incompatibility of metamorphic grade with the occurrence of smectite, the general association of chlorite and smectite, and the textural relations collectively show that dioctahedral smectite is derived through replacement of trioctahedral chlorite. Such replacement occurs on a regional basis and demonstrates that caution must be used in interpreting the occurrence of smectite in pelites as being due to prograde processes. Alteration of trioctahedral chlorite under oxidizing conditions due to introduction of phreatic water after uplift of the Betic Cordillera is proposed as the cause of formation of smectite.  相似文献   
23.
The photodegradation of naphthalene (NPH), chosen as a model of polynuclear aromatic pollutants, has been studied in the presence of a layer of four water-insoluble inorganic solids which can be found in the troposphere (TiO2, Fe2O3, muscovite, and a fly ash sample). Direct photolysis of NPH is negligible at >340 nm. Dark adsorption of NPH on TiO2 (mainly anatase, nonporous, 50 m2 g–1) at 293 K corresponds to a surface coverage ofca. 50% at equilibrium. Under these conditions (saturated surface), the stationary-state photocatalytic degradation reaches 0.4 molecule nm–2 h–1 (>340 nm, radiant fluxca. 22 mW cm–2). Dioxygen is required and its partial pressure in air is such that the degradation is zero order in O2. Water vapor markedly increases the rate. The other particulates have also an effect, less important than that of TiO2, however quite noticeable with respect to surface area unit for the fly ash sample which contains 3.2% Fe2O3. Apart from 1,4-naphthoquinone, which is the main intermediate product in all cases, 2-naphthol, phthalide, phthaldialdehyde, phthalic acid, acetophenone, benzaldehyde, benzoic acid are also formed on dry TiO2. Depending on their volatility, these compounds are transferred to the gas phase or remain principally adsorbed on the solid particles where they are further transformed. For instance, phthalic acid (or anhydride) and benzoic acid are generated from 1,4-naphthoquinone. Degradation mechanisms are briefly discussed.  相似文献   
24.
In this paper analytical expressions are derived for the temporal variations ofJ 2 andJ 22 due to the tides of the solid Earth, taking into account only the deformation of the mantle, and employing a procedure already used by the authors in their Hamiltonian theory of the Earth's rotation, which obtain the necessary parameters in a direct way by integration of those provided by a selected model of Earth interior.Numerical tables giving the periodic variation of coefficients are given, as well as a new prediction for UT1. For J 2 and J 22 the amplitudes reach such a magnitude that both two variations should not be ignored in studies involving the analysis of highly precise satellite tracking data. Moreover, the possibility of improving our knowledge of the value of those harmonic coefficients in only a more exact digit appears as to be strongly dependent on the limitations in the theoretical modeling of the variations of the inertia tensor due to solid tides.  相似文献   
25.
Chlorite and berthierine occur through alteration of cordierite within enclaves of metamorphic rocks transformed by the Sierra Albarrana pegmatites. The coexistence of both phyllosilicates allows us to study their stability relationships and to compare their chemical compositions. Samples showing incipient replacement of cordierite by small cryptocrystalline aggregates can be identified by X-ray diffraction (XRD) as berthierine with small quantities of chlorite. Electron Microprobe (EMP) analyses give mixed compositions of berthierine and cordierite. Samples with extensive replacement of cordierite by aggregates show similar characteristics to those with incipient replacement, but some small crystals are present. The last type of sample shows complete replacement of cordierite by crystals showing optical properties of chlorite and EMPA compositions coherent with chlorite or berthierine. Their XRD pattern corresponds to chlorite and their high resolution transmission electron microscopy (HRTEM) images only show perfect sequences of 14 Å lattice fringes. The cryptocrystalline aggregates of the samples with incipient and extensive replacement present coexistent areas of 14 Å and 7 Å lattice fringes that are intergrown at different levels: (1) large areas (> 1 m) of 7 Å layers; (2) packets of 7 Å layers between 14 Å layer areas, with visible 7 Å to 14 Å lateral changes; (3) random mixed-layers 7 Å/14 Å. Chlorite is the final stable product of alteration of cordierite, with berthierine as an intermediate metastable phase. Energy dispersive X-ray spectrometry microanalyses of 14 Å, 7 Å and (14+7) Å areas show lack of systematic differences in chemical compositions between both phyllosilicates which may be considered as true polymorphs.  相似文献   
26.
The extractable organic matter of 10 immature samples from a marl bed of one evaporitic cycle of the Vena del Gesso sediments (Gessoso-solfifera Fm., Messinian, Italy) was analyzed quantitatively for free hydrocarbons and organic sulphur compounds. Nickel boride was used as a desulphurizing agent to recover sulphur-bound lipids from the polar and asphaltene fractions. Carbon isotopic compositions (delta vs PDB) of free hydrocarbons and of S-bound hydrocarbons were also measured. Relationships between these carbon skeletons, precursor biolipids, and the organisms producing them could then be examined. Concentrations of S-bound lipids and free hydrocarbons and their delta values were plotted vs depth in the marl bed and the profiles were interpreted in terms of variations in source organisms, 13 C contents of the carbon source, and environmentally induced changes in isotopic fractionation. The overall range of delta values measured was 24.7%, from -11.6% for a component derived from green sulphur bacteria (Chlorobiaceae) to -36.3% for a lipid derived from purple sulphur bacteria (Chromatiaceae). Deconvolution of mixtures of components deriving from multiple sources (green and purple sulphur bacteria, coccolithophorids, microalgae and higher plants) was sometimes possible because both quantitative and isotopic data were available and because either the free or S-bound pool sometimes appeared to contain material from a single source. Several free n-alkanes and S-bound lipids appeared to be specific products of upper-water-column primary producers (i.e. algae and cyanobacteria). Others derived from anaerobic photoautotrophs and from heterotrophic protozoa (ciliates), which apparently fed partly on Chlorobiaceae. Four groups of n-alkanes produced by algae or cyanobacteria were also recognized based on systematic variations of abundance and isotopic composition with depth. For hydrocarbons probably derived from microalgae, isotopic variations are well correlated with those of total organic carbon. A resistant aliphatic biomacromolecule produced by microalgae is, therefore, probably an important component of the kerogen. These variations reflect changes in the depositional environment and early diagenetic transformations. Changes in the concentrations of S-bound lipids induced by variations in conditions favourable for sulphurization were discriminated from those related to variations in primary producer assemblages. The water column of the lagoonal basin was stratified and photic zone anoxia occurred during the early and middle stages of marl deposition. During the last stage of the marl deposition the stratification collapsed due to a significant shallowing of the water column. Contributions from anaerobic photoautotrophs were apparently associated with variations in depth of the chemocline.  相似文献   
27.
We discuss the main mechanisms affecting the dynamical evolution of Near-Earth Asteroids (NEAs) by analyzing the results of three numerical integrations over 1 Myr of the NEA (4179) Toutatis. In the first integration the only perturbing planet is the Earth. So the evolution is dominated by close encounters and looks like a random walk in semimajor axis and a correlated random walk in eccentricity, keeping almost constant the perihelion distance and the Tisserand invariant. In the second integration Jupiter and Saturn are present instead of the Earth, and the 3/1 (mean motion) and v 6 (secular) resonances substantially change the eccentricity but not the semimajor axis. The third, most realistic, integration including all the three planets together shows a complex interplay of effects, with close encounters switching the orbit between different resonant states and no approximate conservation of the Tisserand invariant. This shows that simplified 3-body or 4-body models cannot be used to predict the typical evolution patterns and time scales of NEAs, and in particular that resonances provide some fast-track dynamical routes from low-eccentricity to very eccentric, planet-crossing orbits.On leave from the Department of Mathematics, University of Pisa, Via Buonarroti 2, 56127 Pisa, Italy, thanks to the G. Colombo fellowships of the European Space Agency.  相似文献   
28.
New thermal profiles of Jupiter are retrieved from recent far infrared spectral measurements and for H2 mixing ratios varying from 0.8 to 0.94. The effective temperature corresponding to the inferred thermal profile is 123.15 ± 0.35°K. Far-infrared brightness temperature spectra computed from these profiles are compared to experimental data including measurements made at high spectral resolution in the NH3ν2 band at 10 μm and in NH3 pure rotational bands between 40 and 110 μm. It is found that a strong depletion of NH3 does occur in the Jovian stratosphere and that ammonia seems to be undersaturated in the upper troposphere.  相似文献   
29.
The impulsive phases of three flares that occurred on April 10, May 21, and November 5, 1980 are discussed. Observations were obtained with the Hard X-ray Imaging Spectrometer (HXIS) and other instruments aboard SMM, and have been supplemented with Hα data and magnetograms. The flares show hard X-ray brightenings (16–30 keV) at widely separated locations that spatially coincide with bright Hα patches. The bulk of the soft X-ray emission (3.5–5.5 keV) originates from in between the hard X-ray brightenings. The latter are located at different sides of the neutral line and start to brighten simultaneously to within the time resolution of HXIS. Concluded is that:
  1. The bright hard X-ray patches coincide with the footpoints of loops.
  2. The hard X-ray emission from the footpoints is most likely thick target emission from fast electrons moving downward into the dense chromosphere.
  3. The density of the loops along which the beam electrons propagate to the footpoints is restricted to a narrow range (109 < n < 2 × 1010 cm-3), determined by the instability threshold of the return current and the condition that the mean free path of the fast electrons should be larger than the length of the loop.
  4. For the November 5 flare it seems likely that the acceleration source is located at the merging point of two loops near one of the footpoints.
It is found that the total flare energy is always larger than the total energy residing in the beam electrons. However, it is also estimated that at the time of the peak of the impulsive hard X-ray emission a large fraction (at least 20%) of the dissipated flare power has to go into electron acceleration. The explanation of such a high acceleration efficiency remains a major theoretical problem.  相似文献   
30.
We study the spatial and temporal characteristics of the 3.5 to 30.0 keV emission in a solar flare on April 10, 1980. The data were obtained by the Hard X-ray Imaging Spectrometer aboard the Solar Maximum Mission Satellite. It is complemented in our analysis with data from other instruments on the same spacecraft, in particular that of the Hard X-ray Burst Spectrometer.Key results of our investigation are: (a) Continuous energy release is needed to substain the increase of the emission through the rising phase of the flare, before and after the impulsive phase in hard X-rays. The energy release is characterized by the production of hot (5 × 107 T 1.5 × 108 K) thermal regions within the flare loop structures. (b) The observational parameters characterizing the impulsive burst show that it is most likely associated with non-thermal processes (particle acceleration). (c) The continuous energy release is associated with strong chromospheric evaporation, as evidenced in the spectral line behavior determined from the Bent Crystal Spectrometer data. Both processes seem to stop just before flare maximum, and the subsequent evolution is most likely governed by the radiative cooling of the flare plasma.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号