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21.
Scott M. MCLENNAN 《Meteoritics & planetary science》2003,38(6):895-904
Abstract— Basaltic shergottites display a systematic decrease in K/Th, K/U, and K/La ratios with increasing K content. These trends are interpreted as mixing lines between relatively young martian magmas derived from highly depleted mantle sources and an ancient large‐ion lithophile (LIL) element‐enriched crustal component. One implication of this is that a substantial fractionation of these ratios occurs during the early crustal differentiation on Mars. Isotopic evidence from SNC meteorites and compositional data from Pathfinder and orbital gamma ray spectroscopy suggest that in excess of 50% of the LIL element complement of Mars resides in the crustal reservoir. If so, the primitive mantle of Mars is significantly more volatile‐depleted (i.e., lower K/Th, K/U, K/La) than previously thought but probably (though not necessarily) still less volatile‐depleted than the primitive mantle of the Earth. The La/Th ratios of virtually all SNC meteorites are subchondritic, including those with the most severe LREE‐depletion. Extrapolation of the basaltic shergottite trend suggests that both the depleted mantle end member and the enriched crustal end member have subchondritic La/Th ratios. This is in contrast with the Earth where basalts from LIL element‐depleted sources such as MORB have superchondritic La/Th ratios, complementary to the subchondritic ratios of the continental crust. Accordingly, assuming that the refractory elements are in chondritic proportions for the Mars primitive mantle, an additional major geochemical reservoir must exist on Mars that may not yet have been sampled. 相似文献
22.
23.
Methane, a potential biosignature, has recently been detected in the martian atmosphere. This Note focuses on field investigations/operational simulations and laboratory studies which resulted in successful detection of methane within arid terrestrial soils, as distinct from the usual methanogen environment, but in at least partial analogy to martian conditions. 相似文献
24.
A frequent goal of decompaction analysis is to reconstruct histories of basin subsidence and tectonic loading. In marine environments, eustatic and paleobathymetric uncertainties limit the resolution of these reconstructions. Whereas in the terrestrial basins, these ambiguities are absent, it is still necessary to account for depositional slopes between localities in order to analyze three-dimensional patterns of subsidence. We define two end-members for depositional surfaces: aggradation and progradation. The relative importance of either end-member is a function of the interplay between the rate of net sediment accumulation and the rate of basin subsidence. The models predict the patterns of major drainages (transverse versus longitudinal) and the way in which provenance should be reflected within different portions of a basin. Consequently, paleocurrent and provenance data from the ancient stratigraphic record can be used to distinguish between these endmembers. The subhorizontal depositional surfaces that dominate during times of aggradation provide a well defined reference frame for regional analysis of decompacted stratigraphies and related subsidence. Depositional slopes during progradation can not be as precisely specified, and consequently yield greater uncertainties in reconstructions of subsidence. These models are applied to the Mio-Pliocene foreland basin of the northwestern Himalaya, where sequences of isochronous strata have been analyzed throughout the basin. These time-controlled data delineate a distinctive evolution from largely aggradational to largely progradational depositional geometries as deformation progressively encroaches on the foreland. Such a reconstruction of past depositional surfaces provides a well constrained reference frame for subsequent integration of subsidence histories from throughout the foreland.
Zusammenfassung Ein häufiges Ziel der Dekompaktionsanalyse ist es die Beckenabsenkung und die tektonische Belastung zu rekonstruieren. In marinen Ablagerungsräumen limitieren eustatische und paläobathymetrische Unsicherheiten die Auflösung der Rekonstruktion. Bei terrestrischen Becken fehlen diese Zweideutigkeiten; es ist aber trotzdem notwendig, Rechenschaft über den Ablagerungshang zwischen verschiedenen Lokalitäten abzulegen, um dreidimensionale Subsidenzmuster zu analysieren. Wir definieren zwei Endglieder von Ablagerangsflächen: Aggradation und Progradation. Die relative Wichtigkeit des jeweiligen Endglieds ist eine Funktion des Zusammenspiels zwischen der Nettorate der Sedimentakkumulation und der Beckensubsidenz. Die Modelle sagen die Hauptentwässerungsmuster (quer- oder längsverlaufend) vorher, sowie den Weg in dem die Sedimentherkunft innerhalb verschiedener Bereiche des Beckens berücksichtigt werden sollte. Folglich können Paläoströmungs- und Herkunftsdaten alter stratigraphischer Überlieferungen benutzt werden, um zwischen den Endgliedern zu unterscheiden. Die subhorizontale Ablagerungsfläche welche zur Zeit der Aggradation dominant ist, liefert einen gut definierten Referenzrahmen für die regionale Analyse von dekomprimierten Formationen und der damit verknüpften Subsidenz. Ablagerangshänge während Progradation können nicht präzise spezifiziert werden und beinhalten daher größere Unsicherheiten bei der Rekonstruktion der Subsidenz. Diese Modelle wurden übertragen auf das miozäne bis pliozäne Vorgebirgsbecken des nordwestlichen Himalayas, wo Sequenzen von isochronen Schichten durch das gesamte Becken analysiert werden konnten. Diese zeitkontrollierten Daten schildern eine ganz bestimmte Entwicklung, die von einer hauptsächlich aggradierenden zu einer progradierenden Ablagerangsgeometrie verlief, während der die Deformation schrittweise in Richtung Vorland übergriff. Diese Rekonstruktion von ehemaligen Ablagerangsflächen liefert einen guten Referenzrahmen für die folgende Integration der Subsidenzgeschichte des gesamten Vorlands.
Résumé L'analyse de décompaction a souvent pour but de reconstituer l'histoire de la subsidence d'un bassin et de la charge tectonique. Dans les milieux marins, de telles reconstitutions sont limitées par des incertitudes de caractère eustatique et paléobathymétrique. Par contre, ces ambiguïtés ne se présentent pas dans le cas des bassins continentaux, où il convient néanmoins de tenir compte de la pente de la surface de dépôt entre les divers points considérés pour établir un schéma tridimensionnel de la subsidence. Nous définissons deux situations extrêmes pour les surfaces de dépôt: l'aggradation et la progradation. L'importance relative de ces deux extrêmes est fonction de l'interaction entre le taux d'accumulation net des sédiments et le taux de subsidence du bassin. Les modèles prévoient la répartition des drainages principaux (transverse ou longitudinal) et la manière dont l'origine des sédiments peut se répercuter dans les diverses parties d'un bassin. Il en résulte que des informations fournies par les relevés stratigraphiques à propos des paléocourants et de la source des sédiments peuvent être utilisées pour faire la distinction entre les deux cas extrêmes. Les surfaces de dépôt subhorizontales, qui prédominent pendant les périodes d'aggradation, fournissent un bon cadre de référence pour les analyses régionales de formations décompactées et de la subsidence qui leur est associée. Les surfaces de dépôt inclinées qui se présentent au cours des progradations ne peuvent pas être définies de manière aussi précise et engendrent par conséquent plus d'incertitude dans la reconstitution de la subsidence. Les auteurs appliquent ces modèles au bassin mio-pliocène d'avant-pays de l'Himalaya nord-occidental, dans lequel des séquences de couches isochrones ont été suivies à travers tout le bassin. Ces données, chronologiquement définies, fournissent l'image d'une évolution nette, depuis des géométries typiques d'aggradation jusqu' à des géométries typiques de progradation, au fur et à mesure de l'emprise progressive de la déformation sur l'avant-pays. Une telle reconstitution des surfaces de dépôt anciennes fournit un bon cadre de référence en vue de l'intégration ultérieure de l'histoire de la subsidence dans l'ensemble de l'avant-pays.
. . ; , , . « » « ». . , , . , , , . , , . , . , . , , . .相似文献
25.
Charles H. Nelson Douglas S. Hall Francis C. Fekel Robert E. Fried Richard E. Lines Helen C. Lines 《Astrophysics and Space Science》1991,182(1):1-17
Photometry of HD 155638=V792 Her has been analyzed to determine the elements of this totally eclipsing RS CVn binary. The light variation outside eclipse was found to have a period of 27d.07±0d.07, which is slightly different from the 27d.5384±0d.0045 orbital period. Analysis of the eclipses was achieved by a modification of the Russell-Merrill technique. With the aid of radial velocity measures, absolute elements were obtained for the hot and cool stars, respectively;R
h=2.58R
,R
c=12.28R
,M
h=1.40M
,M
c=1.46M
,i=80o.61 and velocity semi-amplitudesK
c=48.36 km s–1±0.79 km s–1, andK
h=50.50 km s–1±0.33 km s–1. The apparent magnitudes areV
h=9
m
.73 andV
c=8
m
.48. The distance to HD 155638 was estimated to be 310 parsecs. 相似文献
26.
Andreas G. Mueller Gregory C. Hall Alexander A. Nemchin Holly J. Stein Robert A. Creaser Douglas R. Mason 《Mineralium Deposita》2008,43(3):337-362
The Granny Smith (37 t Au production) and Wallaby deposits (38 t out of a 180 t Au resource) are located northeast of Kalgoorlie,
in 2.7 Ga greenstones of the Eastern Goldfields Province, the youngest orogenic belt of the Yilgarn craton, Western Australia.
At Granny Smith, a zoned monzodiorite–granodiorite stock, dated by a concordant titanite–zircon U–Pb age of 2,665 ± 3 Ma,
cuts across east-dipping thrust faults. The stock is fractured but not displaced and sets a minimum age for large-scale (1 km)
thrust faulting (D2), regional folding (D1), and dynamothermal metamorphism in the mining district. The local gold–pyrite
mineralization, controlled by fractured fault zones, is younger than 2,665 ± 3 Ma. In augite–hornblende monzodiorite, alteration
progressed from a hematite-stained alkali feldspar–quartz–calcite assemblage and quartz–molybdenite–pyrite veins to a late
reduced sericite–dolomite–albite assemblage. Gold-related monazite and xenotime define a U–Pb age of 2,660 ± 5 Ma, and molybdenite
from veins a Re–Os isochron age of 2,661 ± 6 Ma, indicating that mineralization took place shortly after the emplacement of
the main stock, perhaps coincident with the intrusion of late alkali granite dikes. At Wallaby, a NE-trending swarm of porphyry
dikes comprising augite monzonite, monzodiorite, and minor kersantite intrudes folded and thrust-faulted molasse. The conglomerate
and the dikes are overprinted by barren (<0.01 g/t Au) anhydrite-bearing epidote–actinolite–calcite skarn, forming a 600-m-wide
and >1,600-m-long replacement pipe, which is intruded by a younger ring dike of syenite porphyry pervasively altered to muscovite
+ calcite + pyrite. Skarn and syenite are cut by pink biotite–calcite veins, containing magnetite + pyrite and subeconomic
gold–silver mineralization (Au/Ag = 0.2). The veins are associated with red biotite–sericite–calcite–albite alteration in
adjacent monzonite dikes. Structural relations and the concordant titanite U–Pb age of the skarn constrain intrusion-related
mineralization to 2,662 ± 3 Ma. The main-stage gold–pyrite ore (Au/Ag >10) forms hematite-stained sericite–dolomite–albite
lodes in stacked D2 reverse faults, which offset skarn, syenite, and the biotite–calcite veins by up to 25 m. The molybdenite
Re–Os age (2,661 ± 10 Ma) of the ore suggests a genetic link to intrusive activity but is in apparent conflict with a monazite–xenotime
U–Pb age (2,651 ± 6 Ma), which differs from that of the skarn at the 95% confidence level. The time relationships at both
gold deposits are inconsistent with orogenic models invoking a principal role for metamorphic fluids released during the main
phase of compression in the fold belt. Instead, mineralization is related in space and time to late-orogenic, magnetite-series,
high-Mg monzodiorite–syenite intrusions of mantle origin, characterized by Mg/(Mg + FeTOTAL) = 0.31–0.57, high Cr (34–96 ppm), Ni (22–63 ppm), Ba (1,056–2,321 ppm), Sr (1,268–2,457 ppm), Th (15–36 ppm), and rare earth
elements (total REE: 343–523 ppm). At Wallaby, shared Ca–K–CO2 metasomatism and Th-REE enrichment (in allanite) link Au–Ag mineralization in biotite–calcite veins to the formation of the
giant epidote skarn, implicating a Th + REE-rich syenite pluton at depth as the source of the oxidized hydrothermal fluid.
At Granny Smith, lead isotope data and the Rb–Th–U signature of early hematite-bearing wall-rock alteration point to fluid
released by the source pluton of the differentiated alkali granite dikes. 相似文献
27.
R. Scott Anderson Renata B. Jass Jaime L. Toney Craig D. Allen Marcey Hess Julianna Fessenden 《Quaternary Research》2008,69(2):263-275
Chihuahueños Bog (2925 m) in the Jemez Mountains of northern New Mexico contains one of the few records of late-glacial and postglacial development of the mixed conifer forest in southwestern North America. The Chihuahueños Bog record extends to over 15,000 cal yr BP. An Artemisia steppe, then an open Picea woodland grew around a small pond until ca. 11,700 cal yr BP when Pinus ponderosa became established. C/N ratios, δ13C and δ15N values indicate both terrestrial and aquatic organic matter was incorporated into the sediment. Higher percentages of aquatic algae and elevated C/N ratios indicate higher lake levels at the opening of the Holocene, but a wetland developed subsequently as climate warmed. From ca. 8500 to 6400 cal yr BP the pond desiccated in what must have been the driest period of the Holocene there. C/N ratios declined to their lowest Holocene levels, indicating intense decomposition in the sediment. Wetter conditions returned after 6400 cal yr BP, with conversion of the site to a sedge bog as groundwater levels rose. Higher charcoal influx rates after 6400 cal yr BP probably result from greater biomass production rates. Only minor shifts in the overstory species occurred during the Holocene, suggesting that mixed conifer forest dominated throughout the record. 相似文献
28.
Pedro J. Marenco Frank A. Corsetti Douglas E. Hammond Alan J. Kaufman David J. Bottjer 《Chemical Geology》2008,247(1-2):124-132
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition. 相似文献
29.
Imad A.M. Ahmed Neil M.J. Crout Scott D. Young 《Geochimica et cosmochimica acta》2008,72(6):1498-1512
Time-dependent sorption and desorption of Cd on calcite was studied over 210 days utilizing 109Cd as a tracer to distinguish between ‘labile’ and ‘non-labile’ forms of sorbed Cd. Stabilizing the calcite suspensions for 12 months under atmospheric PCO2 and controlled temperature was necessary to reliably follow Cd dynamics following initial sorption. Results revealed time-dependant Cd sorption and marked desorption hysteresis by calcite under environmentally relevant conditions. Data obtained were fitted to a first-order kinetic model and a concentric shell diffusion model. Both models described the progressive transfer of Cd2+ to a less reactive form within calcite and subsequent desorption of Cd subject to different initial contact times. The kinetic model provided a better fit to the combined sorption and desorption data (R2 = 0.992). It differentiates between two ‘pools’ of sorbed Cd2+ on calcite, ‘labile’ and ‘non-labile’, in which labile sorbed Cd is in immediate equilibrium with the free Cd2+ ion activity in solution whereas non-labile Cd is kinetically restricted. For the diffusion model (R2 = 0.959), the rate constants describing Cd dynamics in calcite produced a half-life for Cd desorption of ∼175 d, for release to a ‘zero-sink’ solution. Results from this study allow comment on the likely mechanisms occurring at the calcite surface following long-term Cd sorption. 相似文献
30.
The current study provides an investigation of abiotic reduction of an oversaturated uranyl solution driven by iron nanoparticle oxidation. The reactivity of nano-scale zero-valent iron (ZVI) under mildly oxic conditions (1.2% O2 and 0.0017% CO2) was studied in 1000 ppm uranyl solution in the pH range 3-7, at reaction times from 10 min to 4 h. Reductive precipitation of UO2 was observed as the main process responsible for the removal of uranium from solution with the kinetics of reaction becoming increasingly favourable at higher pH. Despite working with an oversaturated uranium solution, the precipitation of UO2 occurred in preference to precipitation of UO3·2H2O (metaschoepite) at reaction times between 1 and 4 h and for uranyl solutions initially set up at pH ?5. Characterisation of both solid and solution phases was performed using X-ray photoelectron spectroscopy (XPS), focused ion beam (FIB) imaging, X-ray diffraction (XRD) and inductively coupled plasma atomic emission spectroscopy (ICP-AES). 相似文献