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Zhengtong Xie Peter R. Voke Paul Hayden Alan G. Robins 《Boundary-Layer Meteorology》2004,111(3):417-440
A family of wall models is proposed that exhibits moresatisfactory performance than previousmodels for the large-eddy simulation (LES) of the turbulentboundary layer over a rough surface.The time and horizontally averaged statistics such asmean vertical profiles of windvelocity, Reynolds stress, turbulent intensities, turbulentkinetic energy and alsospectra are compared with wind-tunnel experimental data.The purpose of the present study is to obtain simulatedturbulent flows that are comparable with wind-tunnelmeasurements for use as the wind environment for thenumerical prediction by LES of source dispersion in theneutral atmospheric boundary layer. 相似文献
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Terence Edward Smith Matthew Thirlwall Paul Eric Holm Michael John Harris 《Island Arc》2004,13(1):73-94
Abstract On the island of Mustique, fresh and propylitized olivine–plagioclase–clinopyroxene basalt, plagioclase–clinopyroxene–orthopyroxene and plagioclase–clinopyroxene–amphibole andesite lavas and minor intrusions are interbedded with Oligocene pyroclastic and epiclastic rocks. Chemical data show that two isotopically identical, but chemically different, suites of lava are present: (i) the OPXS (87Sr/86Sr 0.70403–0.70454; 143Nd/144Nd 0.512952–0.512986; δ18Ocpx 5.49 and 5.61), comprising basalts and orthopyroxene‐bearing andesites; and (ii) the AMPHS (87Sr/86Sr 0.70401–0.70457; 143Nd/144Nd 0.512981–0.513037; δ18Ocpx 5.54), made up of basalts and amphibole‐bearing andesites. The OPXS has higher contents of TiO2, P2O5, light rare earth elements, Sm, Pb, Th, U, Zr, Y and Nb, and higher La/Yb ratios than the AMPHS. The isotopic data suggest that both suites formed from melts derived from the same subduction‐modified depleted mantle source as the volcanic rocks of nearby St Vincent and Bequia, and the northern islands of the Lesser Antilles Arc. The immobile trace element contents, and La/Yb ratios, of the OPXS are indicative of ~10% partial melting of the source, whereas those of the AMPHS are indicative of ~25% partial melting. The within‐suite chemical variation of the OPXS is consistent with ~45% fractional crystallization of its intratelluric mineral assemblages, and that of the AMPHS is consistent with the removal of ~65% of its intratelluric assemblages. Experimental evidence suggests that both suites of basalt crystallized at pressures <8 kbar from melts containing 1–2 wt% water. After extensive fractional crystallization, the andesites crystallized at pressures between approximately 5 and 2 kbar. The OPXS magmas appear to have lost more of their water content than the AMPHS magmas. Thus, the OPXS andesites formed from melts with an estimated water content of 2–3 wt%, whereas the AMPHS andesites formed from melts containing at least 4.5 wt% water. 相似文献
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A common assumption in the geological analysis of modern reefs is that coral community zonation seen on the surface should also be found in cores from the reef interior. Such assumptions not only underestimate the impact of tropical storms on reef facies development, but have been difficult to test because of restrictions imposed by narrow‐diameter cores and poor recovery. That assumption is tested here using large‐diameter cores recovered from a range of common zones across three Campeche Bank reefs. It is found that cores from the reef‐front, crest, flat and rubble‐cay zones are similar in texture and coral composition, making it impossible to recognize coral assemblages that reflect the surface zonation. Taphonomic signatures imparted by variations in encrustation, bioerosion and cementation, however, produce distinct facies and delineate a clear depth zonation. Cores from the reef‐front zone (2–10 m depth) are characterized by sections of Acropora palmata cobble gravel interspersed with sections of in‐place (but truncated) A. palmata stumps. Upper surfaces of truncated colonies are intensely bioeroded by traces of Entobia isp. and Gastrochaenolites isp. and encrusted by mm‐thick crustose corallines before colony regeneration and, therefore, indicate punctuated growth resulting from a hurricane‐induced cycle of destruction and regeneration. Cores from the reef crest/flat (0–2 m depth) are also characterized by sections of hurricane‐derived A. palmata cobble‐gravels as well as in‐place A. palmata colonies. In contrast to the reef front, however, these cobble gravels are encrusted by cm‐thick crusts of intergrown coralline algae, low‐relief Homotrema and vermetids, bored by traces of Entobia isp. and Trypanites isp. and coated by a dense, peloidal, micrite cement. Cores from the inter‐ to supratidal rubble‐cay zone (+0–5 m) are only composed of A. palmata cobble gravels and, although clasts show evidence of subtidal encrustation and bioerosion, these always represent processes that occurred before deposition on the cay. Instead, these gravels are distinguished on the basis of their limited bioerosion and marine cements, which exhibit fabrics formed in the intertidal zone. These results confirm that hurricanes have a major influence on facies development in Campeche Bank reefs. Instead of reflecting the surface coral zonation, each facies records a distinctive, depth‐related set of taphonomic processes, which reflect colonization, alteration and stabilization following the production of new substrates by hurricanes. 相似文献
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Improved Platinum-Group Element Extraction by NiS Fire Assay from Chromitite Ore Samples Using a Flux Containing Sodium Metaphosphate 总被引:1,自引:0,他引:1
Many chromite-rich rocks contain relatively high concentrations of the platinum-group elements (PGE). In many cases, the phases carrying PGE occur as either platinum-group minerals (PGM) or as base metal sulfides in solid solution in sulfides. In some cases, such as the UG-2 unit of the Bushveld Complex, the PGM are occluded inside chromite grains. Chromites are notably difficult to dissolve in most fluxes and if the chromite contains some PGM the possibility exists that not all the PGE will be recovered during fusion. In this work, shortcomings in published methods of analysis based on the nickel sulfide fire assay procedure were investigated and a new procedure developed based on the addition of sodium metaphosphate to the fusion mixture. Optimum composition of the fusion mixture was found to be 10 g sodium metaphosphate and 9 g silica to 10 g sample, 15 g sodium carbonate, 30 g lithium tetraborate, 7.5 g nickel and 4.5 g sulfur to achieve complete dissolution of chromite grains. The new flux mixture was evaluated by the analysis of reference material CHR-Pt+ (which is known to contain PGM inside chromite grains) and no undissolved chromite grains were found in the glassy slag. Analysis of the nickel sulfide beads from this fire assay using neutron activation analysis showed similar results for Rh and Ru when compared with published conventional true (or accepted) values, while Au, Ir, Os, Pd and Pt values determined here were 10 to 30% higher than the corresponding published conventional true values. It was concluded that the addition of sodium metaphosphate improved chromite dissolution in the flux and appears to improve PGE recovery. 相似文献