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1.
The variability of rainfall-dependent streamflow at catchment scale modulates many ecosystem processes in wet temperate forests. Runoff in small mountain catchments is characterized by a quick response to rainfall pulses which affects biogeochemical fluxes to all downstream systems. In wet-temperate climates, water erosion is the most important natural factor driving downstream soil and nutrient losses from upland ecosystems. Most hydrochemical studies have focused on water flux measurements at hourly scales, along with weekly or monthly samples for water chemistry. Here, we assessed how water and element flows from broad-leaved, evergreen forested catchments in southwestern South America, are influenced by different successional stages, quantifying runoff, sediment transport and nutrient fluxes during hourly rainfall events of different intensities. Hydrograph comparisons among different successional stages indicated that forested catchments differed in their responses to high intensity rainfall, with greater runoff in areas covered by secondary forests (SF), compared to old-growth forest cover (OG) and dense scrub vegetation (CH). Further, throughfall water was greatly nutrient enriched for all forest types. Suspended sediment loads varied between successional stages. SF catchments exported 455 kg of sediments per ha, followed by OG with 91 kg/ha and CH with 14 kg/ha, corresponding to 11 rainfall events measured from December 2013 to April 2014. Total nitrogen (TN) and phosphorus (TP) concentrations in stream water also varied with rainfall intensity. In seven rainfall events sampled during the study period, CH catchments exported less nutrients (46 kg/ha TN and 7 kg/ha TP) than SF catchments (718 kg/ha TN and 107 kg/ha TP), while OG catchments exported intermediate sediment loads (201 kg/ha TN and 23 kg/ha TP). Further, we found significant effects of successional stage attributes (vegetation structure and soil physical properties) and catchment morphometry on runoff and sediment concentrations, and greater nutrients retention in OG and CH catchments. We conclude that in these southern hemisphere, broad-leaved evergreen temperate forests, hydrological processes are driven by multiple interacting phenomena, including climate, vegetation, soils, topography, and disturbance history.  相似文献   
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A new procedure to separate the instrumental and atmospheric components of stray light is presented. It is based on the dependence of the aureole's atmospheric component on the air mass and is applied to measurements taken with the Vacuum Newton Telescope (VNT) at the Observatorio del Teide (Tenerife). The resulting instrumental part is independent of the air mass.The variation of both components with wavelength is also studied. The instrumental component shows no dependence on wavelength, in contrast to the atmospheric one which is greater in the blue than in the red.It is concluded that observations with air masses larger than two will probably be strongly affected by stray light.  相似文献   
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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   
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This paper reports new geochemical data on dissolved major and minor constituents in surface waters and ground waters collected in the Managua region (Nicaragua), and provides a preliminary characterization of the hydrogeochemical processes governing the natural water evolution in this area. The peculiar geological features of the study site, an active tectonic region (Nicaragua Depression) characterized by active volcanism and thermalism, combined with significant anthropogenic pressure, contribute to a complex evolution of water chemistry, which results from the simultaneous action of several geochemical processes such as evaporation, rock leaching, mixing with saline brines of natural or anthropogenic origin. The effect of active thermalism on both surface waters (e.g., saline volcanic lakes) and groundwaters, as a result of mixing with variable proportions of hyper-saline geothermal Na–Cl brines (e.g., Momotombo geothermal plant), accounts for the high salinities and high concentrations of many environmentally-relevant trace elements (As, B, Fe and Mn) in the waters. At the same time the active extensional tectonics of the Managua area favour the interaction with acidic, reduced thermal fluids, followed by extensive leaching of the host rock and the groundwater release of toxic metals (e.g., Ni, Cu). The significant pollution in the area, deriving principally from urban and industrial waste-water, probably also contributes to the aquatic cycling of many trace elements, which attain concentrations above the WHO recommended limits for the elements Ni (∼40 μg/l) and Cu (∼10 μg/l) limiting the potential utilisation of Lake Xolotlan for nearby Managua.  相似文献   
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Several mechanisms have been proposed to account for the rotation of the nearly north-south abyssal hill fabric formed on the East Pacific Rise north of the Easter Microplate to the nearly east-west trends in the northern microplate interior. Proposed mechanisms include rigid microplate rotation, transform fault – parallel shear, and bookshelf faulting during the transfer of lithosphere from the Nazca Plate to the microplate. We used a submersible magnetometer on a NAUTILE dive program to measure the magnetic vector rotation of a pillow basalt and dike spur near Pito Deep, the present location of the tip of the propagating rift system that created the microplate. Our results, although too limited to draw strong conclusions from, suggest clockwise rotations of the seafloor magnetic vectors inconsistent with the transform-parallel shear model, and larger than can be explained solely by rigid microplate rotation.  相似文献   
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