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581.
The Newania carbonatite complex of Rajasthan, India is one of the few dolomite carbonatites of the world, and oddly, does not contain alkaline silicate rocks thus providing a unique opportunity to study the origin and evolution of a primary carbonatite magma. In an attempt to characterize the mantle source, the source of carbon, and the magmatic and post-magmatic evolution of Newania carbonatites, we have carried out a detailed stable carbon and oxygen isotopic study of the complex. Our results reveal that, in spite of being located in a metamorphic terrain, these rocks remarkably have preserved their magmatic signatures in stable C and O isotopic compositions. The δ13C and δ18O variations in the complex are found to be results of fractional crystallization and low temperature post-magmatic alteration suggesting that like other carbonatites, dolomite carbonatites too fractionate isotopes of both elements in a similar fashion. The major difference is that the fractional crystallization of dolomite carbonatites fractionates oxygen isotopes to a larger extent. The modes of δ13C and δ18O variations in the complex, ?4.5?±?1‰ and 7?±?1‰, respectively, clearly indicate its mantle origin. Application of a multi-component Rayleigh isotopic fractionation model to the correlated δ13C versus δ18O variations in unaltered carbonatites suggests that these rocks have crystallized from a CO2 + H2O fluid rich magma, and that the primary magma comes from a mantle source that had isotopic compositions of δ13C ~ ?4.6‰ and δ18O ~ 6.3‰. Such a mantle source appears to be a common peridotite mantle (δ13C = ?5.0?±?1‰) whose carbon reservoir has insignificant contribution from recycled crustal carbon. Other Indian carbonatites, except for Amba Dongar and Sung Valley that are genetically linked to Reunion and Kerguelen plumes respectively, also appear to have been derived from similar mantle sources. Through this study we establish that dolomite carbonatites are generated from similar mantle source like other carbonatites, have comparable evolutionary history irrespective of their association with alkaline silicate rocks, and may remain resistant to metamorphism. 相似文献
582.
The ophiolitic rocks of Naga Hills-Andaman belt occur as rootless slices, gently dipping over the Paleogene flyschoid sediments,
the presence of blue-schists in ophiolite melange indicates an involvement of the subduction process. Subduction was initiated
prior to mid-Eocene as proved by the contemporaneous lower age limit of ophiolite-derived cover sediment as against the accreted
ophiolites and olistostromal trench sediment. During the late Oligocene terminal collision between the Indian and Sino-Burmese
blocks, basement slivers from the Sino-Burmese block, accreted ophiolites and trench sediments from the subduction zone were
thrust westward as nappe and emplaced over the down-going Indian plate. The geometry of the ophiolites and the presence of
a narrow negative gravity anomaly flanking their map extent, run counter to the conventional view that the Naga-Andaman belt
marks the location of the suture. The root-zone of the ophiolite nappe representing the suture is marked by a partially-exposed
eastern ophiolite belt of the same age and gravity-high zone, passing through central Burma-Sumatra-Java.
The ophiolites of the Andaman and Naga Hills are also conventionally linked with the subduction activity, west of Andaman
islands. This activity began only in late Miocene, much later than onland emplacement of the ophiolites; it further developed
west of the suture in its southern part. Post-collisional northward movement of the Indian plate subparallel to the suture,
also developed leaky dextral transcurrent faults close to the suture and caused Neogene-Quatemary volcanism in central Burma
and elsewhere. 相似文献
583.
The atmospheric general circulation model EC-EARTH-IFS has been applied to investigate the influence of both a reduced and a removed Arctic sea ice cover on the Arctic energy budget and on the climate of the Northern mid-latitudes. Three 40-year simulations driven by original and modified ERA-40 sea surface temperatures and sea ice concentrations have been performed at T255L62 resolution, corresponding to 79?km horizontal resolution. Simulated changes between sensitivity and reference experiments are most pronounced over the Arctic itself where the reduced or removed sea ice leads to strongly increased upward heat and longwave radiation fluxes and precipitation in winter. In summer, the most pronounced change is the stronger absorption of shortwave radiation which is enhanced by optically thinner clouds. Averaged over the year and over the area north of 70° N, the negative energy imbalance at the top of the atmosphere decreases by about 10?W/m2 in both sensitivity experiments. The energy transport across 70° N is reduced. Changes are not restricted to the Arctic. Less extreme cold events and less precipitation are simulated in sub-Arctic and Northern mid-latitude regions in winter. 相似文献
584.
Variability in dissolved organic matter fluorescence and reduced sulfur concentration in coastal marine and estuarine environments 总被引:1,自引:0,他引:1
Sarah G.S. DePalmaW. Ray Arnold James C. McGeerD. George Dixon D. Scott Smith 《Applied Geochemistry》2011,26(3):394-404
Fluorescence characterization of dissolved organic matter (DOM) and measurements of Cr-reducible sulfide (CRS) are presented for 72 coastal marine and estuarine water samples obtained from the USA and Canada. Each sample is identified according to source: terrigenous, autochthonous, wastewater or mixed. Fluorescence data are resolved into contributions from humic, fulvic, tyrosine and tryptophan-like fluorophores. Humic and fulvic-like fluorophores correlate well with dissolved organic C (DOC) (r2 = 0.73 and 0.71, respectively) but tyrosine and tryptophan-like fluorophores show no correlation with DOC. Quality factors are identified by normalization of fluorescence contributions to DOC. Humic and fulvic components show no statistical differences between sources but the amino acid-like fluorescence quality factors show significant variations between source, with highest values for autochthonous sources (0.07 ± 0.01 arbitrary fluorescence units per mg of C) versus low values (0.015 ± 0.005) for terrigenous source waters. CRS concentrations are highly variable from 0.07 ± 0.01 to 7703 ± 98 nM and do no correlate with DOC except when terrigenous source waters (n = 13) are separated out from the total sample set (r2 = 0.55). There is an open question in the literature; does DOC source matter in terms of protective effects towards metal toxicity? Here is shown that DOC molecular-level quality does vary and that this variation is mostly in terms of the contributions of amino acids to total fluorescence. 相似文献