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991.
Gold and silver are ubiquitous, sometimes minor but economically important metals in massive base metal sulfide ores. Their content, proportions and distribution in the ores depend on complex, interrelated factors of their source, mobilization, transport and deposition.Different types of these deposits are formed by similar seafloor hydrothermal systems operating, however, in widely differing tectono-stratigraphic environments which span a spectrum from ensimatic-oceanic, through continent-margin to ensialic-continental ones. Like those of the base metals, the proportions and distribution of the precious metals in the ores vary regionally with these changing depositional environments. This suggests that precious metal content of the sub-seafloor rocks in which the generative fluids circulate is one factor that governs the amounts and distribution in the ores. The lithology of these source-rocks is also important. Pillowed, tholeiitic basalts have high permeability, golddepleted crystalline pillow interiors and relatively gold-rich palagonitic rims, and are consequently particularly favorable sources.Mobilization of gold from the sub-seafloor rocks may require basalt-water, and/or carbonaceous sediment-water reactions to produce strongly reduced bisulfide, carbonyl or cyanide complexes that promote gold transport. Chloride complexing and transport are less important for gold but more so for silver and the base metals.Seafloor hydrothermal discharge at shallow depth is commonly accompanied by boiling, steamblast explosions in the vent and resulting deep penetration and mixing of cool, oxygenated seawater with rising hot, reduced metalliferous fluid. This results in deposition of both chloride- and isulfide-complexed gold at depth and centrally in the footwall stockwork or in copper ore in the base of the massive body. Chloride-complexed silver, stable to lower temperatures, is carried farther and deposited with higher-level and more distal, massive zinc-lead ores. Boiling in deep water, however, although possible, is rare. This fact minimizes deep fluid mixing and allows transport of lower temperaturestable, bisulfide-complexed gold to the seafloor and outward from the vent. Gold too, is then deposited with the shallower, distal, massive zinc-lead-silver ore. Late-stage changes in fluid Eh, salinity and activity of sulfur during evolution of the generative hydrothermal system, and by discharge through previously deposited, early stage sulfides around the vent also cause diagenetic remobilization of gold, moving it to shallower, more distal locations in the system. In combination, these relationships explain the three associations of gold in primary, in-situ massive sulfide deposits; in central, deep footwall stockwork mineralization with or without copper, in central copper ore in the base of the massive body and in shallow, peripheral pyritic zinclead-silver ore.Primary, in-situ ore near the vent is sometimes reworked by seafloor density flows which transport clasts of the primary sulfides down-slope, mix them with rock and sedimentary detritus and redeposit them to form secondary, transported ore. Gold, like iron and the base metals, is diluted during this clastic transport. But silver and barite may be enriched indicating transport in the density flows not only as clasts of primary ore but partly also m solution in the hydrothermal fluids that, in this case, must have lubricated the density flows.
Zusammenfassung Gold- und Silbervorkommen in massiven Metallsulfid-Lagerstätten sind stets ökonomisch wichtige Metalle, auch wenn sie nur in geringen Konzentrationen vorliegen. Der Gehalt an diesen Metallen und ihre Verteilung innerhalb der Lagerstätte hängt von komplexen, sich gegenseitig beeinflussenden Faktoren wie Metallquelle, Art der Mobilisation, Transport und Fällung ab.Unterschiedliche Lagerstättentypen werden von ähnlichen hydrothermalen Systemen auf den Ozeanböden gebildet. Die tektonostratigraphischen Environments unterscheiden sich dabei allerdings beträchtlich; sie befinden sich in ensimatisch-ozeanischen, kontinentalrandlichen und ensialischkontinentalen Bereichen. Innerhalb dieser regional wechselnden Ablagerungsbedingungen variiert Konzentration und Verteilung der Edelmetalle in den Lagerstätten wie bei den einfachen Metallen. Dies bedeutet, daß der Gehalt an Edelmetallen der Gesteine, die den Meeresboden unterlagern und durch die die metallhaltigen Lösungen zirkulieren, ein Faktor ist, der Menge und Verteilung der Metalle in der Lagerstätte steuert. Ebenso ist die Lithologie dieser Gesteine von Bedeutung. Als besonders gut geeignete Quellen gelten kissenartige tholeitische Basalte mit hoher Permeabilität, goldarmen Kisseninneren und relativ goldreichem palagonitischem Rand.Um das Gold aus diesen Gesteinen mobilisieren zu können, bedarf es einer Reaktion zwischen Basalt und Wasser und/oder eines karbonatischen Sediments mit Wasser, um stark reduziertes Bisulfid, Carbonyl-oder Cyanidkomplexe zu bilden, die den Goldtransport ermöglichen. Chlorid-Komplexbildung und -Transport sind zwar wichtig für Silber und einfache Metalle, für Gold spielen sie nur eine untergeordnete Rolle.Der Austritt hydrothermaler Lösungen an Ozeanböden in geringer Tiefe wird in der Regel von Sieden und explosionsartigem Dampfaustritt begleitet und führt deshalb zu einem tiefen Eindringen und Durchmischen von kaltem, sauerstoffreichen Meereswasser mit den aufsteigenden heißen, reduzierten metallischen Lösungen. Daher kommt es zur Fällung von sowohl an Chloridkomplexe als auch an Bisulfidkomplexe gebundenem Gold. Diese Ausfällung findet in größerer Tiefe statt und zwar hauptsächlich im liegenden Stockwerk oder mit Kupfer zusammen an der Basis der massiven Lagerstätte. An Chloridkomplexe gebundenes Silber ist auch bei niedrigeren Temperaturen stabil, wird also weiter transportiert und in einem höheren Niveau in distal gelegenen Blei-Zink-Lagerstätten gefällt. In größeren Wassertiefen kommt es seltener zu dem beobachteten Sieden der austretenden Lösungen. Diese Tatsache reduziert das Durchmischen der Lösungen in größeren Tiefen und ermöglicht den Transport von Gold, das an Bisulfidkomplexe gebunden ist. In diesem Fall ist die Verbindung auch bei niedrigeren Temperaturen noch stabil also transportfähig und kann bis zum Meeresboden oder außerhalb des Schlotes in Lösung bleiben. Dabei kann das Gold zusammen mit Blei, Zink und Silber in mehr distalen Lagerstätten angereichert werden. Späte Änderungen in Eh, Salinität und Schwefelaktivität der Lösungen während der Entwicklung des hydrothermalen Systems, sowie der Austritt durch früher abgelagerte den Schlot umgebende Sulfide, können eine diagenetische Gold-Remobilisation auslösen. Auch dabei kann das Metall zu in geringer Tiefe liegenden, distalen Ablagerungsorten transportiert werden. Berücksichtigt man alle Faktoren, so erklären diese Verhältnisse die drei möglichen Goldvorkommen in primären, in-situ vorliegenden Sulfid-Lagerstätten: Mit Kupfer vergesellschaftet, allerdings nicht unbedingt, zentral im liegenden Stockwerk; an der Basis der Kupferlagerstätte und in geringer Tiefe in Verbindung mit peripheren Blei-Zink-Silber-Vorkommen.Primäre, in-situ neben Schloten vorkommende Lagerstätten werden in einigen Fällen von meeresbodennahen Masseströmen aufgearbeitet. Diese transportieren Sulfidkomponenten, die während des Transports mit Sediment und Gesteinsbruchstücken vermischt und schließlich als sekundäre sedimentäre Lagerstätte abgelagert werden. Durch diesen Transport und die Mischung der Klastika wird die Goldkonzentration in der späteren Lagerstätte stark reduziert. Silber und Barit können dagegen in Ausnahmefällen während des Transports angereichert werden, da diese Komponenten nicht nur als Sulfidbruchstücke transportiert werden, sondern auch in Lösung in den hydrothermalen Lösungen vorhanden sein können. Diese Lösungen dienen in solchen Fällen den Masseströmen als Gleithorizont.

Résumé Dans les gisements de sulfures métalliques massifs, l'or et l'argent sont des métaux ubiquistes, parfois mineurs, mais toujours d'importance économique. Leur teneur et leur distribution dans les corps minéralisés dépendent de facteurs complexes, en relation les uns avec les autres, tels que: leur source, leur mobilité, leurs modalités de transport et de dépôt.A partir des mêmes systèmes hydrothermaux en action sur le fond de la mer, divers types de gisements peuvent être engendrés, selon leur environnement tectono-stratigraphique: océanique ensimatique, de marge continentale ou continental ensialique. Les teneurs et la répartition des métaux précieux, comme celle des autres métaux varient régionalement selon ces divers milieux. Ceci suggère que le contenu en métaux précieux dans les roches sous-jacentes au fond marin à travers lesquelles circulent les solutions minéralisantes est un facteur qui détermine leurs teneurs et leurs répartitions dans les minerais. La lithologie de ces roches-sources est également importante. Une source particulièrement significative est représentée par les coussins des basaltes tholéiitiques, très perméables, avec leur coeur pauvre en or et leur couronne palagonitique relativement riche.Le lessivage de l'or dans les roches situées sous le fond marin peut impliquer des réactions eau-basalte et/ou eausédiments carbonatés, réactions susceptibles d'engendrer les bisulfures très réduits et les complexes carbonés ou cyanurés qui permettent le transport de l'or. Le transport par complexes chlorurés joue un rôle subordoné dans le cas de l'or, mais important dans le cas de l'argent et des autres métaux.L'arrivée de solutions hydrothermales sur les fonds marins peu profonds est d'ordinaire accompagnée d'ébullitons et d'émissions explosives de vapeur, ce qui provoque la pénétration profonde d'eau de mer froide et oxygénée et son mélange avec les fluides métallifères chauds et réducteurs ascendants. Il en résulte le dépôt de complexes aurifères bisulfurés et chlorurés. Cette précipitation s'opère en profondeur, particulièrement dans les roches sous-jacentes ou dans le minerai de cuivre, à la base des corps minéralisés massifs. L'argent des complexes chlorurés, stables à plus basse température, est transporté plus loin et se dépose, en situation plus distale, dans les minerals massifs de Pb-Zn. Dans les mers profondes, l'ébullition, sans être impossible, est néanmoins un phénomène rare; cette circonstance minimise le mélange des fluides en profondeur et permet le transport de l'or jusqu'à la surface du fond et même loin des évents sous la forme de complexes bisulfurés stables à basse température. L'or est alors déposé en situation distale peu profonde avec les minerals massifs de Zn-Pb-Ag. Des modifications tardives d'Eh, de salinité et d'activité du soufre dans les solutions au cours de l'évolution du système hydrothermal, de même que le lessivage des sulfures déjà accumulés autour des évents entraînent une remobilisation diagénétique de l'or vers des situations distales d'eau peu profonde. La combinaison de ces divers facteurs permet d'expliquer les trois occurrences de l'or dans les dépôts in situ de sulfures massifs primaires: dans les parties centrales des masses sous-jacentes en association ou non avec le Cu, à la base des corps minéralisés en Cu, et à faible profondeur, en liaison avec les gisements périphériques de Pb-Zn-Ag.Les gisements primaires, formés in situ près des évents sont parfois remaniés par des courants de densité, qui emportent des clastes de sulfures, les mélangent aux débris sédimentaires et les redéposent sous forme de minerais secondaires. De tels transports provoquent la dilution de l'or, en même temps que celle du fer et des autres métaux. Par contre, l'argent et la barite peuvent subir un enrichissement car leur transport dans les courants de densité ne s'effectue pas seulement sous forme de clastes, mais également en solution dans des fludies hydrothermaux, lesquels, dans ce cas, contribuent à lubrifier le courant de densité.

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992.
Until now a simple Photometric Sunspot Index (PSI) model was used (e.g. Willsonet al., 1981) to describe the contribution of sunspots to the solar irradiance deficit measurement by ACRIM. In this work we replace this model by a photometry of sunspot pictures for the period of 19 August to 4 September, 1980 taking into account the individual features, like lightbridges or umbral dots, of each spot. The main results of this preliminary analysis are: (1) theA u/A p ratios and alsos the values vary in a wide range and are by no means constant as in the PSI model; (2) the general trend of the irradiance deficit from our analysis agrees well with the ACRIM measurements; (3) on some days there are differences of more than 50% between the deficits derived from our measurements and from the PSI model.Paper presented at the 11th Eurpean Regional Astronomical Meetings of the IAU on New Windows to the Universe, held 3–8 July, 1989, Tenerife, Canary Islands, Spain  相似文献   
993.
We analyze the propagation features of synchrotron radiation of a charge moving with a gyrating helix trajectory (3-dimensional) in a magnetoplasma. We found that a new factor (1+ cot ) should be included into the relevant spectrum radiation formulae and the usual relativistic factor has to be modified as , ifv <v g , the radiative energy are more concentrated along the velocity of the moving charge; but ifv>v g, the direction of maximum energy cone deviates from the direction of the moving charge.  相似文献   
994.
At Delft Geotechnics the technique of ground-penetrating radar is in use for the detection of buried objects such as pipes. To enable us to give our ‘measurements in the field’ a more quantitative interpretation than can be deduced from these alone, a series of experiments has been started under well-defined conditions. A cylindrical vessel containing water simulates wet soil. Mounted horizontally above the water surface is a pulsed triangular half-wave dipole which is used as a transmitting antenna (TA). It has a carrier-frequency of about 160 MHz and a pulse repetition-frequency of about 50 kHz. A movable receiving dipole (‘probe’) in the water measures the transverse, mutually orthogonal Eφ,- and Eθ-components of the pulses as a function of probe-position (r, θ, φ) and of the height h of the TA above the water surface. When these pulses are Fourier-transformed, the transverse electric fields Eφ and Eθ at 200 MHz are obtained. The resulting field patterns are compared with computational results on the basis of the theory of the continuous wave, infinitesimal electric dipole (‘point dipole’). It can be concluded that:
  • 1 Far-field conditions have not fully developed at a depth of about 2.50 m, the largest value of the radius r at which field patterns were measured, although it represents a distance of about 15 wavelengths.
  • 2 The attenuation constant of the tapwater used, as deduced from E-field measurements for θ= 0, 2.50 m < r < 2.75 m, is slightly less than the value measured using a network analyser and air line combination, in agreement with (1).
  • 3 E φ field patterns calculated using the value of the conductivity σ corresponding to the former value of the attenuation constant agree reasonably well with the measured patterns for r≤ 2.50 m and for θ < 20° at all antenna heights considered. Calculated Eφ patterns do not agree so well with the measured patterns when h is close to zero. With increasing height the agreement inproves.
  • 4 In accordance with the theory of the point-dipole, the angular distribution of the radiation patterns of the TA becomes wider as the frequency decreases.
  • 5 The normalized underwater pulse-spectra shift to lower frequencies with increasing r. This can be explained since the attenuation constant of the water rises with rising frequency.
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995.
Observations of the vertical profile of hydrogen fluoride (HF) vapor in the stratosphere and of the vertical column amounts of HF above certain altitudes were made using a variety of spectroscopic instruments in the 1982 and 1983 Balloon Intercomparison Campaigns. Both emission instruments working in the far infrared spectral region and absorption instruments using solar occultation in the 2.5m region were employed. No systematic differences were seen in results from the two spectral regions. A mean profile from 20–45 km is presented, with uncertainties ranging from 20% to 50%. Total columns measured from ground and from 12 km are consistent with the profile if the mixing ratio for HF is small in the tropophere and low stratosphere.  相似文献   
996.
A liquid jet of 90 m diameter and variable length has been utilized to determine absorption rates and, hence, mass accommodation coefficients , of atmospheric trace gases. The compounds investigated are HCl (0.01), HNO3 (0.01), N2O5 (0.005), peroxyacetyl nitrate (>0.001), and HONO (0.005). It is concluded that the absorption of these trace gases by liquid atmospheric water is not significantly retarded by interfacial mass transport. The strengths and limitations of the liquid jet technique for measuring mass accommodation coefficients are explored.  相似文献   
997.

Correspondence

Reply to the comment by Addo Van Pul and John H. Van Boxel on a first order closure scheme to describe counter gradient momentum transport in plant canopies by Li, Miller and Lin  相似文献   
998.
Over 200 H, O, Sr, Nd, and Pb isotope analyses, in addition to geologic and petrologic constraints, document the magmatic evolution of the 28.5–19 Ma Latir volcanic field and associated intrusive rocks, which includes multiple stages of crustal assimilation, magma mixing, protracted crystallization, and open- and closed-system evolution in the upper crust. In contrast to data from younger volcanic centers in northern New Mexico, relatively low and restricted primary 18O values (+6.4 to +7.4) rule out assimilation of supracrustal rocks enriched in 18O. Initial 87Sr/86Sr ratios (0.705 to 0.708), 18O values (-2 to-7), and 206Pb/204Pb ratios (17.5 to 18.4) of metaluminous precaldera volcanic rocks and postcaldera plutonic rocks suggest that most Latir rocks were generated by fractional crystallization of substantial volumes of mantle-derived basaltic magma that had near-chondritic Nd isotope ratios, accompanied by assimilation of crustal material in two main stages: 1) assimilation of non-radiogenic lower crust, followed by 2) assimilation of middle and upper crust by inter-mediate-composition magmas that had been contaminated during the first stage. Magmatic evolution in the upper crust peaked with eruption of the peralkaline Amalia Tuff (26 Ma), which evolved from metaluminous parental magmas. A third stage of late, roofward assimilation of Proterozoic rocks in the Amalia Tuff magma is indicated by trends in initial 87Sr/86Sr and 206Pb/204Pb ratios from 0.7057 to 0.7098 and 19.5 to 18.8, respectively, toward the top of the pre-eruptive magma chamber. Highly evolved postcaldera plutons are generally fine grained and are zoned in initial 87Sr/86Sr and 206Pb/204Pb ratios, varying from 0.705 to 0.709 and 17.8 to 18.6, respectively. In contrast, the coarser-grained Cabresto Lake (25 Ma) and Rio Hondo (21 Ma) plutons have relatively homogeneous initial 87Sr/86Sr and 206Pb/204Pb ratios of approximately 0.7053 and 17.94 and 17.55, respectively. 18O values for all the postcaldera plutons overlap those of the precaldera rocks and Amalia Tuff, except for those for two late-stage rhyolite dikes associated with the Rio Hondo pluton that have 18O values of-8.6 and-9.5; these dikes are the only Latir rocks which may be largely crustal melts.Chemical and isotopic data from the Latir field suggest that large fluxes of mantle-derived basaltic magma are necessary for developing and sustaining large-volume volcanic centers. Development of a detailed model suggests that 6–15 km of new crust may have been added beneath the volcanic center; such an addition may result in significant changes in the chemical and Sr and Nd isotopic compositions of the crust, although Pb isotope ratios will remain relatively unchanged. If accompanied by assimilation, crystallization of pooled basaltic magma near the MOHO may produce substantial cumulates beneath the MOHO that generate large changes in the isotopic composition of the upper mantle. The Latir field may be similar to other large-volume, long-lived intracratonal volcanic fields that fundamentally owe their origins to extensive injection of basaltic magma into the lower parts of their magmatic systems. Such fields may overlie areas of significant crustal growth and hybridization.  相似文献   
999.
The carbon isotopic fractionation between CO2 vapour and sodamelilite (NaCaAlSi2O7) melt over a range of pressures and temperatures has been investigated using solid-media piston-cylinder high pressure apparatus. Ag2C2O4 was the source of CO2 and experimental oxygen fugacity was buffered at hematite-magnetite by the double capsule technique. The abundance and isotopic composition of carbon dissolved in sodamelilite (SM) glass were determined by stepped heating and the 13C of coexisting vapour was determined directly by capsule piercing. CO2 solubility in SM displays a complex behavior with temperature. At pressures up to 10 kbars CO2 dissolves in SM to form carbonate ion complexes and the solubility data suggest slight negative temperature dependence. Above 20 kbars CO2 reacts with SM to form immiscible Na-rich silicate and Ca-rich carbonate melts and CO2 solubility in Na-enriched silicate melt rises with increasing temperature above the liquidus. Measured values for carbon isotopic fractionation between CO2 vapour and carbonate ions dissoived in sodamelilite melt at 1200°–1400° C and 5–30 kbars average 2.4±0.2, favouring13C enrichment in CO2 vapour. The results are maxima and are independent of pressure and temperature. Similar values of 2 are obtained for the carbon isotopic fractionation between CO2 vapour and carbonate melts at 1300°–1400° C and 20–30 kbars.  相似文献   
1000.
The Siljan Ring is a 362-Ma-old impact structure formed in 1700-Ma-old I-type granites. A 6.8-km-deep borehole provides a vertical profile through granites and isolated horizontal diabase sills. Fluid-inclusion thermometry, and oxygen-isotope compositions of vein quartz, granite, diabase, impact melt, and pseudotachylite, reveal a complex history of fluid activity in the Siljan Ring, much of which can be related to the meteorite impact. In granites from the deep borehole, 18O values of matrix quartz increase with depth from near 8.0 at the surface to 9.5 at 5760 m depth. In contrast, feldspar 18O values decrease with depth from near 10 at the surface to 7.1 at 5760 m, forming a pattern opposite to the one defined by quartz isotopic compositions. Values of 18O for surface granites outside the impact structure are distinct from those in near-surface samples from the deep borehole. In the deep borehole, feldspar coloration varies from brick-red at the surface to white at 5760 m, and the abundances of crack-healing calcite and other secondary minerals decrease over the same interval. Superimposed on the overall decrease in alteration intensity with depth are localized fracture zones at 4662, 5415, and 6044 m depth that contain altered granites, and which provided pathways for deep penetration of surface water. The antithetic variation of quartz and feldspar 18O values, which can be correlated with mineralogical evidence of alteration, provides evidence for interaction between rocks and impact-heated fluids (100–300° C) in the upper 2 km of the pluton. Penetration of water to depths below 2 km was restricted by a general decrease in impact-fracturing with depth, and by a 60-m-thick diabase sill at 1500 m depth that may have been an aquitard. At depths below 4 km in the pluton, where water/rock ratios were low, oxygen isotopic compositions preserve evidence for limited high-temperature (>500° C) exchange between alkali feldspar and fluids. The high-temperature exchange may have been a post-impact event involving impact-heated fluids, or a post-magmatic event.  相似文献   
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