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11.
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.
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12.
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
13.
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
14.
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
15.
Multiple sulfur isotope system is a powerful new tracer for atmospheric, volcanic, and biological influences on sulfur cycles in the anoxic early Earth. Here, we report high-precision quadruple sulfur isotope analyses (32S/33S/34S/36S) of barite, pyrite in barite, and sulfides in related hydrothermal and igneous rocks occurring in the ca. 3.5 Ga Dresser Formation, Western Australia. Our results indicate that observed isotopic variations are mainly controlled by mixing of mass-dependently (MD) and non-mass-dependently fractionated (non-MD) sulfur reservoirs. Based on the quadruple sulfur isotope systematics (δ34S-Δ33S-Δ36S) for these minerals, four end-member sulfur reservoirs have been recognized: (1) non-MD sulfate (δ34S = −5 ± 2‰; Δ33S = −3 ± 1‰); (2) MD sulfate (δ34S = +10 ± 3‰); (3) non-MD sulfur (δ34S > +6‰; Δ33S > +4‰); and (4) igneous MD sulfur (δ34S = Δ33S = 0‰). The first and third components show a clear non-MD signatures, thus probably represent sulfate and sulfur aerosol inputs. The MD sulfate component (2) is enriched in 34S (+10 ± 3‰) and may have originated from microbial and/or abiotic disproportionation of volcanic S or SO2. Our results reconfirm that the Dresser barites contain small amounts of pyrite depleted in 34S by 15-22‰ relative to the host barite. These barite-pyrite pairs exhibit a mass-dependent relationship of δ33S/δ34S with slope less than 0.512, which is consistent with that expected for microbial sulfate reduction and is significantly different from that of equilibrium fractionation (0.515). The barite-pyrite pairs also show up to 1‰ difference in Δ36S values and steep Δ36S/Δ33S slopes, which deviate from the main Archean array (Δ36S/Δ33S = −0.9) and are comparable to isotope effects exhibited by sulfate reducing microbes (Δ36S/Δ33S = −5 to −11). These new lines of evidence support the existence of sulfate reducers at ca. 3.5 Ga, whereas microbial sulfur disproportionation may have been more limited than recently suggested. 相似文献
16.
This paper demonstrates the use of dissolution-rate data obtained in the laboratory to indicate the potential quality of effluent from a field-scale oxic limestone drain (OLD) treatment system for neutralization of dilute acidic mine drainage (AMD). Effluent from the Reevesdale Mine South Dip Tunnel, a large source of AMD and base flow to the Wabash Creek and Little Schuylkill River in the Southern Anthracite Coalfield of east-central Pennsylvania, is representative of AMD with low concentrations but high loadings of dissolved Fe, Al and other metals because of a high flow rate. In January 2003, rapid neutralization of the AMD from the Reevesdale Mine was achieved in laboratory tests of its reaction rate with crushed limestone in closed, collapsible containers (Cubitainers). The tests showed that net-alkaline effluent could be achieved with retention times greater than 3 h and that effluent alkalinities and associated dissolution rates were equivalent for Fe(OH)3-coated and uncoated limestone. On the basis of the laboratory results, a flushable OLD containing 1450 metric tons of high-purity calcitic limestone followed by two 0.7-m deep wetlands were constructed at the Reevesdale Mine. During the first year of operation, monthly data at the inflow, outflow and intermediate points within the treatment system were collected (April 2006–2007). The inflow to the treatment system ranged from 6.8 to 27.4 L/s, with median pH of 4.7, net acidity of 9.1 mg/L CaCO3, and concentrations of dissolved Al, Fe and Mn of 1.0, 1.9 and 0.89 mg/L, respectively. The corresponding effluent from the OLD had computed void-volume retention times of 4.5–18 h, with median pH of 6.6, net acidity of −93.2 mg/L CaCO3, and concentrations of dissolved Al, Fe and Mn of <0.1, 0.08 and 0.52 mg/L, respectively. The wetlands below the OLD were effective for retaining metal-rich solids flushed at monthly or more frequent intervals from the OLD, but otherwise had little effect on the effluent quality. During the first year of operation, approximately 43 metric tons of limestone were dissolved and 2 metric tons of Al, Fe and Mn were precipitated within the OLD. However, because of the accumulation of these metals within the OLD and possibly other debris from the mine, the effectiveness of the treatment system declined. Despite the installation of a flush-pipe network at the base of the OLD to remove precipitated solids, the limestone bed clogged near the inflow. Consequently, a large fraction of the AMD bypassed the treatment system. To promote flow through the OLD, the flush pipes were open continuously during the last 4 months of the study; however, this effluent was only partially treated because short-circuiting through the pipes decreased contact between the effluent and limestone. A reconfiguration of the flow path through the limestone bed from horizontal to vertical upward could increase the limestone surface area exposed to the metal-laden influent, increase the cross-sectional area perpendicular to flow, decrease the flow path for solids removal, and, consequently, decrease potential for clogging. 相似文献
17.
Complete hydrochemical data are rarely reported for coal-mine discharges (CMD). This report summarizes major and trace-element concentrations and loadings for CMD at 140 abandoned mines in the Anthracite and Bituminous Coalfields of Pennsylvania. Clean-sampling and low-level analytical methods were used in 1999 to collect data that could be useful to determine potential environmental effects, remediation strategies, and quantities of valuable constituents. A subset of 10 sites was resampled in 2003 to analyze both the CMD and associated ochreous precipitates; the hydrochemical data were similar in 2003 and 1999. In 1999, the flow at the 140 CMD sites ranged from 0.028 to 2210 L s−1, with a median of 18.4 L s−1. The pH ranged from 2.7 to 7.3; concentrations (range in mg/L) of dissolved (0.45-μm pore-size filter) SO4 (34–2000), Fe (0.046–512), Mn (0.019–74), and Al (0.007–108) varied widely. Predominant metalloid elements were Si (2.7–31.3 mg L−1), B (<1–260 μg L−1), Ge (<0.01–0.57 μg L−1), and As (<0.03–64 μg L−1). The most abundant trace metals, in order of median concentrations (range in μg/L), were Zn (0.6–10,000), Ni (2.6–3200), Co (0.27–3100), Ti (0.65–28), Cu (0.4–190), Cr (<0.5–72), Pb (<0.05–11) and Cd (<0.01–16). Gold was detected at concentrations greater than 0.0005 μg L−1 in 97% of the samples, with a maximum of 0.0175 μg L−1. No samples had detectable concentrations of Hg, Os or Pt, and less than half of the samples had detectable Pd, Ag, Ru, Ta, Nb, Re or Sn. Predominant rare-earth elements, in order of median concentrations (range in μg/L), were Y (0.11–530), Ce (0.01–370), Sc (1.0–36), Nd (0.006–260), La (0.005–140), Gd (0.005–110), Dy (0.002–99) and Sm (<0.005–79). Although dissolved Fe was not correlated with pH, concentrations of Al, Mn, most trace metals, and rare earths were negatively correlated with pH, consistent with solubility or sorption controls. In contrast, As was positively correlated with pH. 相似文献
18.
19.
Coastal sand delivery by a stream in southern California is estimated based on a numerical model which stimulates unsteady flow, sediment transport, and the associated channel adjustments for a stream-delta system. An average annual sediment yield of 51,400 m3/yr is estimated for the San Dieguito River, which drains a semiarid watershed controlled by dams. Of the total sand delivery by the stream, 20.5 percent is contributed from floods greater than the 100-year flood; 17.6 percent from those between the 50- and 100-year events; 28.4 percent from those between the 25- and 50 year floods; and 33.5 percent from those smaller than the 25-year flood. 相似文献
20.
Anaerobic salt marsh sediments were amended with a variety of organic pollutants and the effects on methanogenesis, sulfate reduction and carbon dioxide evolution were examined. Addition of 1000 μg g?1 (dry weight sediment) Arochlor 1221, lindane, endrin, benzene and phenanthrene resulted in no significant effects on the activities studied. Methanogenesis was inhibited by 1000 μg g?1toxaphene, PCP, chlordane, naphthalene, DDT, Kepone and heptachlor and by 100 μg g?1 PCP and toxaphene. At 1000 μg g?1 naphthalene and toxaphene and 100 μg g?1 PCP, a period of initial inhibition of methanogenesis was followed by stimulation relative to controls. Arochlor 1254 (1000 μg g?1) and Temik (500 and 10 μg g?1) stimulated methanogenesis from the outset. Temik at 500 μg g?1 gave the greatest stimulation of methanogenesis (900% of controls) of any of the compounds studied. Sulfate reduction was inhibited by 1000 μg g?1 PCP, toxaphene, naphthalene and chlordane and by 500 μg g?1 atrazine and 100 μg g?1 heptachlor. Sustained inhibition of sulfate reduction by naphthalene, toxaphene and PCP may have contributed to the stimulation of methanogenesis. Carbon dioxide evolution was not significantly affected by most of the compounds studied except for 100 μg g?1 PCP and 1000 μg g?1 aphthalene, each of which gave significant inhibition in only one of three experiments.Concentrations of individual organic pollutants required to cause observable effects were high. It is concluded that, except for highly polluted sediments, methanogenesis, sulfate reduction and CO2 evolution would not be affected by the compounds studied here at concentrations typically found in the environment. 相似文献