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61.
Metal-rich carbonaceous CB chondrites are generally assumed to be materials accreted from the gas–dust plume formed in catastrophic collisions of planetesimals, at least one of which was differentiated into a metal core and silicate shell. Micron-sized inclusions of siliceous alkali-rich glasses associated with sulfides were found in the metal globules of the Sierra Gorda 013 (SG 013), a CBa-like chondrite. These inclusions are unusual carriers of volatile alkalis which are commonly depleted in CB chondrites. The inclusions are presented by two types: (1) Al-bearing Nb-poor glass associated with daubréelite and (2) Nb-bearing Ca,Al,Mg-poor glass associated with an unknown Na-bearing Cr-sulfide. The glass compositions do not correspond to equilibrium condensation, evaporation, or melting. The Nb-bearing glass has a superchondritic Nb/Ta ratio (31) most likely indicating the fractionation of Nb and Ta in the high-temperature gas–dust impact plume due to condensation from vapor or evaporation of precursor Nb-rich particles. The glasses are interpreted as reaction products between refractory plume condensate particles (or possibly planetary or chondritic solids) with relatively low-temperature K-Na-Si-rich gas in oxidized conditions, possibly in a common plume vapor reservoir. Compositional differences indicate that the glasses and sulfides originated from several different sources under different fO2, fS2, and T conditions and were likely combined together and transported to the metal globule formation region by material flows in the heterogeneous impact plume. The glass–sulfide particles were enclosed in the globules aggregated from smaller solid or molten metal grains. The metal globules were further melted during transport to the high-temperature plume region or by plume shockwave heating. Thus, the composition of the glasses, the host metal, and the main mass of SG 013 shows dynamic heterogeneity of physical conditions and impact plume composition after a large-scale planetesimal collision.  相似文献   
62.
Amphibole is widely employed to calculate crystallization temperature and pressure, although its potential as a geobarometer has always been debated. Recently, Ridolfi et al. (Contrib Mineral Petrol 160:45–66, 2010) and Ridolfi and Renzulli (Contrib Mineral Petrol 163:877–895, 2012) have presented calibrations for calculating temperature, pressure, fO2, melt H2O, and melt major and minor oxide composition from amphibole with a large compositional range. Using their calibrations, we have (i) calculated crystallization conditions for amphibole from eleven published experimental studies to examine the problems and the potential of the new calibrations; and (ii) calculated crystallization conditions for amphibole from basaltic–andesitic pyroclasts erupted during the paroxysmal 2010 eruption of Mount Merapi in Java, Indonesia, to infer pre-eruptive conditions. Our comparison of experimental and calculated values shows that calculated crystallization temperatures are reasonable estimates. Calculated fO2 and melt SiO2 content yields potentially useful estimates at moderately reduced to moderately oxidized conditions and intermediate to felsic melt compositions. However, calculated crystallization pressure and melt H2O content are untenable estimates that largely reflect compositional variation in the crystallizing magmas and crystallization temperature and not the calculated parameters. Amphibole from Merapi’s pyroclasts yields calculated conditions of ~200–800 MPa, ~900–1,050 °C, ~NNO + 0.3–NNO + 1.1, ~3.7–7.2 wt% melt H2O, and ~58–71 wt% melt SiO2. We interpret the variations in calculated temperature, fO2, and melt SiO2 content as reasonable estimates, but conclude that the large calculated pressure variation for amphibole from Merapi and many other arc volcanoes is evidence for thorough mixing of mafic to felsic magmas and not necessarily evidence for crystallization over a large depth range. In contrast, bimodal pressure estimates obtained for other arc magmas reflect amphibole crystallization from mafic and more evolved magmas, respectively, and should not necessarily be taken as evidence for crystallization in two reservoirs at variable depth.  相似文献   
63.
This study provides new data on the strontium distribution and behavior in groundwater from the Permian aquifer system, which is used for public water supply in the Velsk region of Arkhangelsk District. We used data from recent sampling of groundwater and host rocks as well as data from previous studies over the last 25 years. Measurements of exchangeable cations obtained in this study will be used in the further thermodynamic calculations and experimental observations.  相似文献   
64.
New data on geology and 21 K–Ar dates of the Late Oligocene–Quaternary basalts in Syria, combined with analysis of the new and previous data are used to reconstruct the volcanic history and relations between it and tectonic events. Volcanism began at the end of Oligocene (26–24 Ma) and was concentrated in the Late Oligocene–Early Miocene along a N-trending band, which stretches from the Jebel Arab (Harrat Ash Shaam) up to Kurd Dagh and southern Turkey. Activity waned in the Middle Miocene (17–12 Ma), but was resumed in the same band in the Tortonian and increased in the Messinian and Early Pliocene (6.3–4 Ma), when volcanism spread to the Shin Plateau and its coastal extension. After a brief hiatus ~ 4–3.5 Ma, volcanism became still more intensive and spread from the N-trending band to the east into the northern margin of the Mesopotamian Foredeep and to the west into the Dead Sea Transform zone. Additional eruptions continued into the Holocene.Volcanism lasted > 25 million years in the Jebel Arab Highland and > 15 million years in the Aleppo Plateau. The long duration of volcanism in the same parts of the moving Arabian plate and absence of records of one-way migration of the activity mean that the magmatic sources moved together with the plate, i.e., they were situated within the lithosphere mantle. Coincidence of the tectonic and volcanic stages of the Arabian plate development proves that volcanic activity depended on the geodynamic situation, caused by the plate motion. Situated within the lithosphere, magmatic sources within this transverse band were possibly caused by thermal and deforming influences of the asthenospheric lateral flow, moved laterally from the Ethiopia–Afar deep superplume.  相似文献   
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67.
N. L. Ivanova 《Astrophysics》1994,37(2):135-137
Results are presented from a spectrophotometric study of SU Aurigae in the continuum and on spectral lines.Translated from Astrofizika, Vol. 37, No. 2, pp. 229–233, April–June, 1994.  相似文献   
68.
Geotectonics - In our study we analyzed the composition of granitoid rocks within the Kongo magmatic zone of the Omolon median mass. The studied calc-alkaline granitoids cut through the Early...  相似文献   
69.
The aim of this study is the synthesis of CuSeO3·2H2O (chalcomenite analog), ZnSeO3·2H2O, and ZnSeO3·H2O and the investigation of their solubility in water. CuSeO3·2H2O has been synthesized from solutions of Cu nitrate and Na selenite, while Zn selenites were synthesized from solutions of Zn nitrate and Na selenite. The samples obtained have been examined with X-ray diffraction and infrared and Raman spectroscopy. The solubility has been determined using the isothermal saturation method in ampoules at 25°C. The solubility has been calculated using the Geochemist’s Workbench (GMB 9.0) software package. Solubility products have been calculated for CuSeO3·2H2O (10–10.63), ZnSeO3·2H2O (10–8.35), and ZnSeO3·H2O (10–7.96). The database used comprises thermodynamic characteristics of 46 elements, 47 base particles, 48 redox pairs, 551 particles in solution, and 624 solid phases. The Eh–pH diagrams of the Zn–Se–H2O and Cu–Se–H2O systems were plotted for the average contents of these elements in underground water in oxidation zones of sulfide deposits.  相似文献   
70.
Four samples (TL5b, TL11h, TL11i, and TL11v) from the pristine collection of the Tagish Lake meteorite, an ungrouped C2 chondrite, were studied to characterize and understand its alteration history using EPMA, XRD, and TEM. We determined that samples TL11h and TL11i have a relatively smaller proportion of amorphous silicate material than sample TL5b, which experienced low‐temperature hydrous parent‐body alteration conditions to preserve this indigenous material. The data suggest that lithic fragments of TL11i experienced higher degrees of aqueous alteration than the rest of the matrix, based on its low porosity and high abundance of coarse‐ and fine‐grained sheet silicates, suggesting that TL11i was present in an area of the parent body where alteration and brecciation were more extensive. We identified a coronal, “flower”‐like, microstructure consisting of a fine‐grained serpentine core and coarse‐grained saponite‐serpentine radial arrays, suggesting varied fluid chemistry and crystallization time scales. We also observed pentlandite with different morphologies: an exsolved morphology formed under nebular conditions; a nonexsolved pentlandite along grain boundaries; a “bulls‐eye” sulfide morphology and rims around highly altered chondrules that probably formed by multiple precipitation episodes during low‐temperature aqueous alteration (≥100 °C) on the parent body. On the basis of petrologic and mineralogic observations, we conclude that the Tagish Lake parent body initially contained a heterogeneous mixture of anhydrous precursor minerals of nebular and presolar origin. These materials were subjected to secondary, nonpervasive parent‐body alteration, and the samples studied herein represent different stages of that hydrous alteration, i.e., TL5b (the least altered) < TL11h < TL11i (the most altered). Sample TL11v encompasses the petrologic characteristics of the other three specimens.  相似文献   
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