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751.
Sarah K. Appleby Martin R. Gillespie Colin M. Graham Richard W. Hinton Grahame J. H. Oliver Nigel M. Kelly 《Contributions to Mineralogy and Petrology》2010,160(1):115-132
In contrast to I-type granites, which commonly comprise infracrustal and supracrustal sources, S-type granites typically incorporate
predominantly supracrustal sources. The initial aim of this study was to identify the sources of three Scottish Caledonian
(~460 Ma) S-type granites (Kemnay, Cove and Nigg Bay) by conducting oxygen, U–Pb and Hf isotope analyses in zircon in order
to characterise one potential end-member magma involved in the genesis of the voluminous late Caledonian (~430–400 Ma) I-type
granites. Field, whole-rock geochemical and isotopic data are consistent with the generation of the S-type granites by melting
their Dalradian Supergroup country rocks. While Hf isotope compositions of magmatic zircon, U–Pb data of inherited zircons,
and high mean zircon δ18O values of 9.0 ± 2.7‰ (2SD) and 9.8 ± 2.0‰ for the Kemnay and Cove granites support this model, the Nigg Bay Granite contains
zircons with much lower δ18O values (6.8 ± 2.1‰), similar to those found in Scottish I-type granites. This suggests that the Nigg Bay Granite contains
low-δ18O material representing either altered supracrustal material, or more likely, an infracrustal source component with mantle-like
δ18O. Mixing trends in plots of δ18O vs. εHf for S-type granite zircons indicate involvement of at least two sources in all three granites. This pilot study
of Scottish Caledonian S-type granites demonstrates that, while field and whole-rock geochemical data are consistent with
local melting of only supracrustal sources, the oxygen isotopic record stored in zircon reveals a much more complex petrogenetic
evolution involving two or more magma sources. 相似文献
752.
Carleton R. Bern Mark A. Brzezinski Charlotte Beucher Oliver A. Chadwick 《Geochimica et cosmochimica acta》2010,74(3):876-5891
Silicon isotope ratios (δ30Si) of bulk mineral materials in soil integrate effects from both silicon sources and processing. Here we report δ30Si values from a climate gradient of Hawaiian soils developed on 170 ka basalt and relate them to patterns of soil chemistry and mineralogy. The results demonstrate informative relationships between the mass fraction of soil Si depletion and δ30Si. In upper (<1 m deep) soil horizons along the climate gradient, Si depletion correlates with decreases of residual δ30Si values in low rainfall soils and increases in high rainfall soils. Strong positive correlation between soil δ30Si and dust-derived quartz and mica content show that both trends are largely controlled by the abundance of these weathering-resistant minerals. The data also lend support to the idea that fractionation of Si isotopes in secondary phases is controlled by partitioning of silicon between dissolved and precipitated products during the initial weathering of primary basalt. Secondary mineral δ30Si values from lower (>1 m deep) soil horizons generally correlate with the isotope fractionation predicted by a study of dissolved Si in basalt-watershed rivers and driven by preferential 28Si removal from the dissolved phase during precipitation. In contrast, after correcting for the influence of dust, secondary mineral Si depletion and δ30Si values in shallow (<1 m deep) soil horizons showed evidence of biocycling induced Si redistribution and substantially lower δ30Si values than predicted. Low δ30Si values in shallow soil horizons compared to predictions can be attributed to repeated fractionation as secondary minerals undergo additional cycles of dissolution and precipitation. Primary mineral weathering, secondary mineral weathering, dust accumulation, and biocycling are major processes in terrestrial Si cycling and these results demonstrate that each can be traced by δ30Si values interpreted in conjunction with mineralogy and measures of Si depletion. 相似文献
753.
High-precision high field strength element partitioning between garnet, amphibole and alkaline melt from Kakanui, New Zealand 总被引:2,自引:0,他引:2
The high field strength elements (HFSE: Zr, Hf, Nb, Ta, and W) are an important group of chemical tracers that are increasingly used to investigate magmatic differentiation processes. Successful modeling of these processes requires the availability of accurate mineral-melt partition coefficients (D). To date, these have largely been determined by ion microprobe or laser ablation-ICP-MS analyses of the run products of high-pressure, high-temperature experiments. Since HFSE are (highly) incompatible, relatively immobile, high-charge, and difficult to ionize, these experiments and their analysis are challenging. Here we explore whether high-precision analyses of natural mineral-melt systems can provide additional constraints on HFSE partitioning.The HFSE concentrations in natural garnet and amphibole and their alkaline host melt from Kakanui, New Zealand are determined with high precision isotope dilution on a multi-collector-ICP-MS. Major and trace element compositions combined with Lu-Hf isotopic systematics and detailed petrographic sample analysis are used to assess mineral-melt equilibrium and to provide context for the HFSE D measurements. The whole-rock nephelinite, ∼1 mm sized amphiboles in the nephelinite, and garnet megacrysts have similar initial Hf isotope ratios with a mean initial 176Hf/177Hf(34 Ma) = 0.282900 ± 0.000026 (2σ). In contrast, the amphibole megacrysts are isotopically distinct (176Hf/177Hf(34 Ma) = 0.282830 ± 0.000011). Rare earth element D values for garnet megacryst-nephelinite melt and ∼1 mm amphibole-nephelinite melt plotted as a function of ionic radii show classic near-parabolic trends that are in excellent agreement with crystal lattice-strain models. These observations are consistent with equilibrium between the whole-rock nephelinite, the ∼1 mm amphibole grains within the nephelinite and the garnet megacrysts.High-precision isotope dilution results for Zr and Hf in garnet (DZr = 0.220 ± 0.007 and DHf = 0.216 ± 0.005 [2σ]), and for all HFSE in amphibole are consistent with previous experimental findings. However, our measurements for Nb and Ta in garnet (DNb = 0.0007 ± 0.0001 and DTa = 0.0011 ± 0.0006 [2σ]) show that conventional methods may overestimate Nb and Ta concentrations, thereby overestimating both Nb and Ta absolute D values for garnet by up to 3 orders of magnitude and underestimating DNb/DTa by greater than a factor of 100. As a consequence, the role of residual garnet in imposing Nb/Ta fractionation may be less important than previously thought. Moreover, garnet DHf/DW = 17 and DNb/DZr = 0.003 imply fractionation of Hf from W and Nb from Zr upon garnet crystallization, which may have influenced short-lived 182Hf-182W and 92Nb-92Zr isotopic systems in Hadean time. 相似文献
754.
The pterodactyloid genus Germanodactylus is relatively poorly known. Two species have been described, although it has been recently suggested (Wang et al., 2008) that they might pertain to different genera. 相似文献
755.
The ensemble Kalman filter has been successfully applied for data assimilation in very large models, including those in reservoir
simulation and weather. Two problems become critical in a standard implementation of the ensemble Kalman filter, however,
when the ensemble size is small. The first is that the ensemble approximation to cross-covariances of model and state variables
to data can indicate the presence of correlations that are not real. These spurious correlations give rise to model or state
variable updates in regions that should not be updated. The second problem is that the number of degrees of freedom in the
ensemble is only as large as the size of the ensemble, so the assimilation of large amounts of precise, independent data is
impossible. Localization of the Kalman gain is almost universal in the weather community, but applications of localization
for the ensemble Kalman filter in porous media flow have been somewhat rare. It has been shown, however, that localization
of updates to regions of non-zero sensitivity or regions of non-zero cross-covariance improves the performance of the EnKF
when the ensemble size is small. Localization is necessary for assimilation of large amounts of independent data. The problem
is to define appropriate localization functions for different types of data and different types of variables. We show that
the knowledge of sensitivity alone is not sufficient for determination of the region of localization. The region depends also
on the prior covariance for model variables and on the past history of data assimilation. Although the goal is to choose localization
functions that are large enough to include the true region of non-zero cross-covariance, for EnKF applications, the choice
of localization function needs to balance the harm done by spurious covariance resulting from small ensembles and the harm
done by excluding real correlations. In this paper, we focus on the distance-based localization and provide insights for choosing
suitable localization functions for data assimilation in multiphase flow problems. In practice, we conclude that it is reasonable
to choose localization functions based on well patterns, that localization function should be larger than regions of non-zero
sensitivity and should extend beyond a single well pattern. 相似文献
756.