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991.
992.
Geology of Ore Deposits - The structure, geochemistry, and U–Pb and Lu–Hf isotopic composition of zircon crystals from garnet granulite xenoliths of the lower crust in the Belomorian... 相似文献
993.
Yakovenchuk V. N. Pakhomovsky Ya. A. Konoplyova N. G. Panikorovskii T. L. Mikhailova Yu. A. Bocharov V. N. Krivovichev S. V. Ivanyuk G. Yu. 《Geology of Ore Deposits》2018,60(7):587-593
Geology of Ore Deposits - Epifanovite, NaCaCu5(PO4)4[AsO2(OH)2] · 7H2O, a new natural copper, sodium and calcium arsenate–phosphate, has been found in a quartz–phosphate pocket... 相似文献
994.
Zubkova N. V. Pekov I. V. Chukanov N. V. Kasatkin A. V. Ksenofontov D. A. Yapaskurt V. O. Britvin S. N. Pushcharovsky D. Yu. 《Geology of Ore Deposits》2018,60(7):594-606
Geology of Ore Deposits - The crystal structure of lemanskiite is determined for the first time (R = 0.019) and the mineral is redefined. Its chemical formula, crystal system, space group and... 相似文献
995.
López-Moro F. J. López-Plaza M. Gutiérrez-Alonso G. Fernández-Suárez J. López-Carmona A. Hofmann M. Romer R. L. 《International Journal of Earth Sciences》2018,107(3):985-1004
International Journal of Earth Sciences - In this study, we report U–Pb Laser Ablation ICP-MS zircon and ID-TIMS monazite ages for peraluminous granitoid plutons... 相似文献
996.
Krylov Alexey A. Hachikubo Akihiro Minami Hirotsugu Pogodaeva Tatyana V. Zemskaya Tamara I. Krzhizhanovskaya Mariya G. Poort Jeffrey Khlystov Oleg M. 《International Journal of Earth Sciences》2018,107(6):2011-2022
International Journal of Earth Sciences - Early diagenetic carbonates are rare in Lake Baikal. Siderite (Fe carbonate) concretions in the sediments were discovered only recently. Here, we discuss... 相似文献
997.
Rao G. Srinivasa Kumar Manish Radhakrishna M. 《International Journal of Earth Sciences》2018,107(6):2191-2207
International Journal of Earth Sciences - The continental breakup history at the northwest continental margin of India remained conjectural due to lack of clearly discernable magnetic anomaly... 相似文献
998.
Ramacciotti Carlos D. Casquet César Baldo Edgardo G. Galindo Carmen Pankhurst Robert J. Verdecchia Sebastián O. Rapela Carlos W. Fanning Mark 《International Journal of Earth Sciences》2018,107(7):2605-2625
International Journal of Earth Sciences - The Western Sierras Pampeanas (WSP) of Argentina record a protracted geological history from the Mesoproterozoic assembly of the Rodinia supercontinent to... 相似文献
999.
Sequestration of organic carbon (OC) in environmental systems is critical to mitigating climate change. Organo-mineral associations, especially those with iron (Fe) oxides, drive the chemistry of OC sequestration and stability in soils. Short-range-ordered Fe oxides, such as ferrihydrite, demonstrate a high affinity for OC in binary systems. Calcium commonly co-associates with OC and Fe oxides in soils, though the bonding mechanism (e.g., cation bridging) and implications of the co-association for OC sequestration remain unresolved. We explored the effect of calcium (Ca2+) on the sorption of dissolved OC to 2-line ferrihydrite. Sorption experiments were conducted between leaf litter-extractable OC and ferrihydrite at pH 4 to 9 with different initial C/Fe molar ratios and Ca2+ concentrations. The extent of OC sorption to ferrihydrite in the presence of Ca2+ increased across all tested pH values, especially at pH ≥ 7. Sorbed OC concentration at pH 9 increased from 8.72 ± 0.16 to 13.3 ± 0.20 mmol OC g?1 ferrihydrite between treatments of no added Ca2+ and 30 mM Ca2+ addition. Batch experiments were paired with spectroscopic studies to probe the speciation of sorbed OC and elucidate the sorption mechanism. ATR-FTIR spectroscopy analysis revealed that carboxylic functional moieties were the primary sorbed OC species that were preferentially bound to ferrihydrite and suggested an increase in Fe-carboxylate ligand exchange in the presence of Ca at pH 9. Results from batch to spectroscopic experiments provide significant evidence for the enhancement of dissolved OC sequestration to 2-line ferrihydrite and suggest the formation of Fe–Ca-OC ternary complexes. Findings of this research will inform modeling of environmental C cycling and have the potential to influence strategies for managing land to minimize OM stabilization. 相似文献
1000.
Jason W. Stuckey Christopher Goodwin Jian Wang Louis A. Kaplan Prian Vidal-Esquivel Thomas P. BeebeJr. Donald L. Sparks 《Geochemical transactions》2018,19(1):6
Minerals constitute a primary ecosystem control on organic C decomposition in soils, and therefore on greenhouse gas fluxes to the atmosphere. Secondary minerals, in particular, Fe and Al (oxyhydr)oxides—collectively referred to as “oxides” hereafter—are prominent protectors of organic C against microbial decomposition through sorption and complexation reactions. However, the impacts of Mn oxides on organic C retention and lability in soils are poorly understood. Here we show that hydrous Mn oxide (HMO), a poorly crystalline δ-MnO2, has a greater maximum sorption capacity for dissolved organic matter (DOM) derived from a deciduous forest composite Oi, Oe, and Oa horizon leachate (“O horizon leachate” hereafter) than does goethite under acidic (pH 5) conditions. Nonetheless, goethite has a stronger sorption capacity for DOM at low initial C:(Mn or Fe) molar ratios compared to HMO, probably due to ligand exchange with carboxylate groups as revealed by attenuated total reflectance-Fourier transform infrared spectroscopy. X-ray photoelectron spectroscopy and scanning transmission X-ray microscopy–near-edge X-ray absorption fine structure spectroscopy coupled with Mn mass balance calculations reveal that DOM sorption onto HMO induces partial Mn reductive dissolution and Mn reduction of the residual HMO. X-ray photoelectron spectroscopy further shows increasing Mn(II) concentrations are correlated with increasing oxidized C (C=O) content (r = 0.78, P < 0.0006) on the DOM–HMO complexes. We posit that DOM is the more probable reductant of HMO, as Mn(II)-induced HMO dissolution does not alter the Mn speciation of the residual HMO at pH 5. At a lower C loading (2 × 102 μg C m?2), DOM desorption—assessed by 0.1 M NaH2PO4 extraction—is lower for HMO than for goethite, whereas the extent of desorption is the same at a higher C loading (4 × 102 μg C m?2). No significant differences are observed in the impacts of HMO and goethite on the biodegradability of the DOM remaining in solution after DOM sorption reaches steady state. Overall, HMO shows a relatively strong capacity to sorb DOM and resist phosphate-induced desorption, but DOM–HMO complexes may be more vulnerable to reductive dissolution than DOM–goethite complexes. 相似文献