全文获取类型
收费全文 | 783篇 |
免费 | 32篇 |
国内免费 | 5篇 |
专业分类
测绘学 | 39篇 |
大气科学 | 123篇 |
地球物理 | 169篇 |
地质学 | 289篇 |
海洋学 | 54篇 |
天文学 | 90篇 |
综合类 | 5篇 |
自然地理 | 51篇 |
出版年
2023年 | 3篇 |
2022年 | 4篇 |
2021年 | 9篇 |
2020年 | 16篇 |
2019年 | 10篇 |
2018年 | 28篇 |
2017年 | 34篇 |
2016年 | 42篇 |
2015年 | 32篇 |
2014年 | 24篇 |
2013年 | 36篇 |
2012年 | 37篇 |
2011年 | 46篇 |
2010年 | 48篇 |
2009年 | 46篇 |
2008年 | 43篇 |
2007年 | 54篇 |
2006年 | 32篇 |
2005年 | 38篇 |
2004年 | 22篇 |
2003年 | 17篇 |
2002年 | 27篇 |
2001年 | 21篇 |
2000年 | 6篇 |
1999年 | 11篇 |
1998年 | 5篇 |
1997年 | 10篇 |
1996年 | 6篇 |
1995年 | 10篇 |
1994年 | 10篇 |
1992年 | 2篇 |
1991年 | 4篇 |
1990年 | 2篇 |
1989年 | 2篇 |
1988年 | 4篇 |
1987年 | 6篇 |
1986年 | 3篇 |
1985年 | 6篇 |
1984年 | 8篇 |
1982年 | 6篇 |
1981年 | 7篇 |
1979年 | 2篇 |
1978年 | 5篇 |
1977年 | 7篇 |
1976年 | 4篇 |
1975年 | 2篇 |
1974年 | 2篇 |
1971年 | 2篇 |
1965年 | 2篇 |
1953年 | 2篇 |
排序方式: 共有820条查询结果,搜索用时 62 毫秒
1.
2.
Veined lithologies are formed by fracturing and sealing processes, with the veins representing former fluid conduits through the rock. Although detailed fieldwork and numerical simulations have provided a better understanding of vein growth, few studies have attempted to seal fractures and generate veins experimentally. In this pilot study, we subjected fractured quartzite to temperature gradients of 45–125 °C under hydrothermal conditions in a static fluid, with the aim of precipitating secondary quartz in the cooler portions of the fracture. Results show that secondary quartz precipitates due to the imposed temperature gradient, causing the initial fracture to seal locally. Although no systematic sealing pattern was observed along the fracture, samples subjected to higher temperatures exhibit a smaller fracture width and appear to have reacted more extensively. Electron microprobe mapping visualizes the spatial distribution of secondary quartz, which contains elevated concentrations of aluminium. 相似文献
3.
Lawrence M. Mayer Peter T. Rahaim William Guerin Stephen A. Macko Les Watling Franz E. Anderson 《Estuarine, Coastal and Shelf Science》1985,20(4):491-503
A variety of measures of organic matter concentration and quality were made on samples collected from the top few mm of intertidal mudflat sediment over the course of a year, in order to assess the relative importance of biological and sedimentological influences on sedimentary organic matter. Winter and summer were times of relatively fine-grained sediment accumulation, caused by biological deposition or stabilization processes and resulting in higher organic matter concentrations. Stable carbon isotope and Br:C ratios indicated a planktonic source of bulk organic matter. Ratios of organic carbon to specific surface area of the sediments were consistent with an organic monolayer coverage of sediment grains. Correction for changing grain size during the year showed no change in the organic concentration per unit surface area, in spite of organic matter inputs by in situ primary production, buildup of heterotroph biomass and mucus coatings, and biodeposition of organic-rich seston. There were also no indications of changes in bulk organic quality, measured as hydrolyzable carbohydrates and amino acids, in response to these biological processes. It is concluded that biological processes on a seasonal time scale affect the bulk organic matter of these sediments via a modulation of grain size rather than creation or decay of organic matter. 相似文献
4.
Relict rock glaciers have considerable potential for contributing to palaeoclimatic reconstruction, but this potential is often undermined by lack of dating control and problems of interpretation. Here we reinvestigate and date four proposed ‘rock glaciers’ in the Cairngorm Mountains and show that the morphology of only one of these appears consistent with that of a true rock glacier produced by creep of underlying ice or ice‐rich sediment. All four features comprise rockslide or rock avalanche runout debris, and the possibility that all four represent unmodified runout accumulations cannot be discounted. Surface exposure dating of the four debris accumulations using cosmogenic 10Be produced uncertainty‐weighted mean ages of 15.4 ± 0.8 ka, 16.2 ± 1.0 ka, 12.1 ± 0.6 ka and 12.7 ± 0.8 ka. All four ages imply emplacement under cold stadial conditions, two prior to the Windermere Interstade of ca. 14.5–12.9 cal. ka BP and two during the Loch Lomond Stade of ca. 12.9–11.5 cal. ka BP. The above ages indicate that paraglacial rock‐slope failure on granite rockwalls occurred within a few millennia after deglaciation. The mean exposure ages obtained for runout debris at two sites – Strath Nethy (16.2 ± 1.0 ka) and Lairig Ghru (15.4 ± 0.8 ka) – are consistent with basal radiocarbon ages from Loch Etteridge, 22 km to the southwest (mean = 15.6 ± 0.3 cal. ka BP) and imply widespread deglaciation of the Cairngorms and adjacent valleys before 15 ka and possibly 16 ka. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
5.
In 1903 the Swiss Federal Research Institute WSL started its first forest hydrology measurements with the aim to deliver a sound scientific basis for the implementation of new forest legislation introduced in Switzerland in 1876. This legislation was triggered by several large floods that occurred in Switzerland, for which a major cause was widely seen as the poor condition of forests at that time. Consequently, hydrologic research at WSL first focused on the influence of forests on floods. In the second half of the 20th century, other hydrological issues such as water quality, snow hydrology and sediment transport complemented the hydrologic research at WSL. Some recent results of this work are presented in three papers joining this introductory paper to mark the 100th anniversary of hydrologic research at WSL. Copyright © 2006 John Wiley & Sons, Ltd. 相似文献
6.
Summary Evaluation of the results of radioactivity monitoring in the southern North Sea between 1977 and 1987 has shown that in the water of the German Bight three areas stand out due to their different ratios between salinity and concentration of dissolved Cs-137 and tritium. While salinity steadily increases with greater distance from the coast, the Cs-137 concentration above 34 PSU (Practical Salinity Unit) increases sharply and shows how far water from the western and central North Sea, contaminated by nuclear reprocessing in Sellafield (Irish Sea), reaches into the German Bight. In the 34 to 32.5 PSU range, the influence can be seen of water contaminated by tritium originating in the rivers Rhein, Maas and Schelde, precipitation and the nuclear reprocessing plant at La Hague (Channel). Below 32.5 PSU, the influence of the influx from the rivers Elbe, Weser and Ems becomes apparent. These rivers are less contaminated with tritium.Assuming that Cs-137 and tritium, like the salinity of sea water, behave conservatively and that the decay-time of these two isotopes is long compared with the time-scale of water exchange in the southern North Sea, the concentration values measured are used to calculate the structure of the water masses in the three areas of the German Bight mentioned above using the mixing principle. Evaporation is taken into account. Results show that beyond 34 PSU, about half the sea water originates in the western central North Sea while the other half comes from the Channel. Below 34 PSU, the first mentioned share amounts only to a few per cent. Results also show that fresh water from the Rhein delta and precipitation, increasing with a decrease in salinity from 34 to 32.5 PSU, accounts for a maximum of 5% each. The fresh water influx into the German Bight via the rivers Elbe, Weser and Ems amounts to app. 11% when the PSU value reaches 29. The calculated portions are the mean values for the observation period. The number of measurements available makes it impossible to distinguish more exactly between the temporal and spatial variability of the amounts of the individual components.The quantity of each calculated portion of sea water also represents the transfer factor of concentration between the nuclide concentration in the source (e. g. the Rhein) and the concentration in the German Bight. In addition, these factors are used to calculate the transfer factors of discharge using the annual drainage rates of the sources. Thus a radioactive discharge rate of 1015 Bq per year into the Rhein would produce a mean activity concentration of 0.34 Bq/l in the German Bight (at a salinity of 33.5 PSU). To verify the calculated transfer factors, tritium concentrations in the German Bight are derived from existing environmental tritium data and the results are compared with the values actually measured.
Transferkaktoren zwischen der Deutschen Bucht und ihren Zuflüssen abgeleitet aus der Tritium- und Cs-137-Aktivitätskonzentration in den beteiligten Gewässern
Zusammenfassung Eine zusammenhängende Auswertung der Meßergebnisse der Radioaktivitätsüberwachung in der südlichen Nordsee über den Zeitraum 1977 bis 1987 hat gezeigt, daß im Wasser der Deutschen Bucht deutlich drei durch den Salzgehalt des Meerwassers und die Konzentration der gelösten Radionuklide charakterisierte Bereiche zu unterscheiden sind.Während der Salzgehalt mit wachsender Entfernung von der Küste stetig zunimmt, steigt die Cs-137-Konzentration oberhalb 34 PSU (Practical Salinity Unit) sprunghaft an und signalisiert die Grenze, bis zu der das durch die Kernbrennstoff-Wiederaufarbeitung in Sellafield (Irische See) kontaminierte Meerwasser der westlichen und mittleren Nordsee in die Deutsche Bucht vordringt. Im Bereich 34 bis 32,5 PSU ist das von Westen zugeführte, stärker Tritium-kontaminierte Wasser aus Rhein, Maas, Schelde und atmosphärischem Niederschlag zu erkennen, an das sich unterhalb 32,5 PSU der geringer mit Tritum kontaminierte Zufluß aus Elbe, Weser und Ems anschließt.Davon ausgehend, daß sich Cs-137 und Tritium wie der Salzgehalt im Meerwasser konservativ verhalten und daß weiterhin die Halbwertzeit des radioaktiven Zerfalls dieser beiden Nuklide lang ist gegenüber den Wasseraustauschzeiten im betrachteten Meeresgebiet, wurden die in der südlichen Nordsee gemessenen sowie aus der Literatur für den Süßwasserbereich entnommenen Konzentrationswerte dazu genutzt, um rechnerisch mit Hilfe des Mischungsgesetzes den Wassermassenaufbau in den drei genannten Salinitätsbereichen in der Deutschen Bucht quantitativ zu bestimmen. Es zeigte sich, daß oberhalb von 34 PSU das Meerwasser aus etwa gleichen Teilen aus der westlichen/mittleren Nordsee und dem Kanal stammt, während unterhalb dieser Salzgehaltsgrenze nur noch mit wenigen Prozentanteilen Wasser aus der mittleren Nordsee zu finden ist. Ferner ergab sich, daß das aus dem Rheinmündungsbiet bzw, aus dem atmosphärischen Niederschlag stammende Süßwasser — mit sinkendem Salzgehalt steigend — bei 32,5 PSU einen maximalen Anteil von jeweils 5% an Meerwasser hat. Der direkte Süßwasserzufluß aus Elbe, Weser und Ems beträgt in die Deutsche Bucht bei 29 PSU ca. 11%.Die berechneten Anteile sind Mittelwerte über den gesamten Beobachtungszeitraum; die Anzahl der Messungen läßt eine genauere Unterscheidung in zeitliche und räumliche Variabilität der Zusammensetzung nicht zu.Die Größe des jeweils bestimmten Anteils am Meerwasser stellt gleichzeitig den Transferfaktor der Konzentration zwischen der Nuklidkonzentration im Ursprungsgewässer (z. B. dem Rhein) und der sich daraus einstellenden Konzentration in der Deutschen Bucht dar. Ferner wurden die Transferfaktoren der Konzentration in Verbindung mit aus der Literatur entnommenen Größen der jährlichen Abflußmengen der Ursprungsgewässer genutzt, um auch die Transferfaktoren der jährlichen Einbringung zu ermitteln. So ergibt die jährliche Einbringung von 1015 Bq eines Nuklides z. B. in den Rhein bei 33,5 PSU in der Deutschen Bucht eine mittlere Konzentration von 0,34 Bq/l.Als Anwendungsbeispiel und zur Überprüfung der Richtigkeit der Transferfaktoren wird die Auswertung des Tritiumauslasses bei La Hague auf die Deutsche Bucht berechnet und mit den gemessenen Werten verglichen.相似文献
7.
Kurt Krenn Christoph Bauer Alexander Proyer Evripidis Mposkos Georg Hoinkes 《Lithos》2008,104(1-4):33-53
A fluid inclusion study on metamorphic minerals of successive growth stages was performed on highly deformed paragneisses from the Nestos Shear Zone at Xanthi (Central Rhodope), in which microdiamonds provide unequivocal evidence for ultrahigh-pressure (UHP) metamorphism. The correlation of fluid inclusion density isochores and fluid inclusion reequilibration textures with geothermobarometric data and the relative chronology of micro- and macro-scale deformation stages allow a better understanding of both the fluid and metamorphic evolution along the P–T–d path. Textural evidence for subduction towards the NE is recorded by the orientation of intragranular NE-oriented fluid inclusion planes and the presence of single, annular fluid inclusion decrepitation textures. These textures occur within quartz “foam” structures enclosed in an earlier generation of garnets with prolate geometries and rarely within recrystallized matrix quartz, and reequilibrated both in composition and density during later stages of exhumation. No fluid inclusions pertaining to the postulated ultrahigh-pressure stage for microdiamond-bearing garnet–kyanite–gneisses have yet been found. The prolate shape of garnets developed during the earliest stages of exhumation that is recorded structurally by (L S) tectonites, which subsequently accommodated progressive ductile SW shearing and folding up to shallow crustal levels. The majority of matrix kyanite and a later generation of garnet were formed during SW-directed shear under plane-strain conditions. Fluid inclusions entrapped in quartz during this stage of deformation underwent density loss and transformed to almost pure CO2 inclusions by preferential loss of H2O. Those inclusions armoured within garnet retained their primary 3-phase H2O–CO2 compositions. Reequilibration of fluid inclusions in quartz aggregates is most likely the result of recrystallization along with stress-induced, preferential H2O leakage along dislocations and planar lattice defects which results in the predominance of CO2 inclusions with supercritical densities. Carbonic fluid inclusions from adjacent kyanite–corundum-bearing pegmatoids and, the presence of shear-plane-parallel fluid inclusion planes within late quartz boudin structures consisting of pure CO2-fluid inclusions with negative crystal shapes, bear witness of the latest stage of deformation by NE-directed extensional shear.This study shows that the textures of early fluid inclusions that formed already during the prograde metamorphic path can be preserved and used to derive information about the kinematics of subduction that is difficult to obtain from other sources. The textures of early inclusions, together with later generations of unaltered primary and secondary inclusions in metamorphic index minerals that can be linked to specific deformation stages and even P–T conditions, are a welcome supplement for the reconstruction of a rather detailed P–T–d path. 相似文献
8.
Combined fluid inclusion microthermometry and microanalysis by laser ablation inductively coupled plasma mass spectrometry
(LA-ICPMS) are used to constrain the hydrothermal processes forming a typical Climax-type porphyry Mo deposit. Molybdenum
mineralisation at Questa occurred in two superimposed hydrothermal stages, a magmatic-hydrothermal breccia and later stockwork
veining. In both stages, texturally earliest fluids were single-phase, of low salinity (~7 wt.% NaClequiv.) and intermediate-density. Upon decompression to ~300 bar, they boiled off a vapour phase, leaving behind a residual brine
(up to 45 wt.% NaClequiv) at temperatures of ~420°C. The highest average Mo concentrations in this hot brine were ~500 μg/g, exceeding the Mo content
of the intermediate-density input fluid by about an order of magnitude and reflecting pre-concentration of Mo by fluid phase
separation prior to MoS2 deposition from the brine. Molybdenum concentrations in brine inclusions, then, decrease down to 5 μg/g, recording Mo precipitation
in response to cooling of the saline liquid to ~360°C. Molybdenite precipitation from a dense, residual and probably sulphide-depleted
brine is proposed to explain the tabular shape of the ore body and the absence of Cu-Fe sulphides in contrast to the more
common Cu-Mo deposits related to porphyry stocks. Cesium and Rb concentrations in the single-phase fluids of the breccia range
from 2 to 8 and from 40 to 65 μg/g, respectively. In the stockwork veins, Cs and Rb concentrations are significantly higher
(45–90 and 110–230 μg/g, respectively). Because Cs and Rb are incompatible and hydrothermally non-reactive elements, the systematic
increase in their concentration requires two distinct pulses of fluid exsolution from a progressively more fractionated magma.
By contrast, major element and ore metal concentrations of these two fluid pulses remain essentially constant. Mass balance
calculations using fluid chemical data from LA-ICPMS suggest that at least 25 km3 of melt and 7 Gt of deep input fluid were necessary to provide the amount of Mo contained in the stockwork vein stage alone.
While the absolute amounts of fluid and melt are uncertain, the well-constrained element ratios in the fluids together with
empirical fluid/melt partition coefficients derived from the inclusion analyses suggest a high water content of the source
melt of ~10%. In line with other circumstantial evidence, these results suggest that initial fluid exsolution may have occurred
at a confining pressure exceeding 5 kbar. The source of the molybdenum-mineralising fluids probably was a particularly large
magma chamber that crystallised and fractionated in the lower crust or at mid-crustal level, well below the shallow intrusions
immediately underlying Questa and other porphyry molybdenum deposits.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
9.
The massive sulfide deposits of the Iberian Pyrite Belt are interbedded with felsic volcanic rocks and shale, and underlain by several thousand meters of siliciclastic sedimentary rocks known as the PQ Group. Isotope geochemistry and regional geology are both consistent with equilibration of the ore-forming fluids with the PQ Group, prior to ore deposition near the former seafloor. The average Cu:Zn:Pb ratio of the PQ Group rocks (ca. 26:55:19) is similar to the weighted average of all the massive sulfide orebodies combined (ca. 25:52:23).The genetic relationship between massive sulfide deposits and a siliciclastic sedimentary metal source is explained here by a thermodynamic model, proposing that mildly reducing redox conditions imposed by equilibration with the sedimentary rocks are most critical for the formation of an effective ore-forming fluid. Relatively metal-rich but organic-poor pyrite-bearing shale undergoing dewatering of saline pore fluids is an effective source for the generation of sulfur-deficient but relatively iron and base metal-rich brines. Thus, we propose that the giant deposits of the Iberian Pyrite Belt owe their existence not to exceptionally metal-enriched (e.g., magmatic) fluids, but to the existence of a fairly ordinary but large metal source in reactive siliciclastic sediments, combined with an underlying igneous heat source and a particularly efficient mechanism of sulfide precipitation by mixing with H2S-rich fluids at or near the seafloor.Essentially similar mineral equilibria are imposed when saline fluids are buffered by typical continental basement rocks. Leaching of retrograde minerals and possibly residual salts from their magmatic or metamorphic prehistory is expected to generate similar, variably metal-rich but relatively sulfide-deficient fluids. Thus, the existence of mildly reducing rocks can be the dominant chemical control in the source of fluids generating many volcanogenic, Irish-type or sedex deposits, many of which are known to precipitate their metal load in response to biogenic sulfide addition at the ore deposition site. 相似文献
10.