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81.
82.
Doklady Earth Sciences - This work presents results of isotope studies of primary igneous and sedimentary rocks of Mawson and Menzies series from the southern Prince Charles Mountains, East...  相似文献   
83.
The surface chemistry of natural wollastonite, diopside, enstatite, forsterite, and albite in aqueous solutions was characterized using both electrokinetic techniques and surface titrations performed for 20 min in batch reactors. Titrations performed in such reactors allow determination of both proton consumption and metal release from the mineral surface as a function of pH. The compositions, based on aqueous solution analysis, of all investigated surfaces vary dramatically with solution pH. Ca and Mg are preferentially released from the surfaces of all investigated divalent metal silicates at pH less than ∼8.5-10 but preferentially retained relative to silica at higher pH. As such, the surfaces of these minerals are Si-rich and divalent metal poor except in strongly alkaline solutions. The preferential removal of divalent cations from these surfaces is coupled to proton consumption. The number of protons consumed by the preferential removal of each divalent cation is pH independent but depends on the identity of the mineral; ∼1.5 protons are consumed by the preferential removal of each Ca atom from wollastonite, ∼3 protons are consumed by the preferential removal of each Mg or Ca atom from diopside or enstatite, and ∼4 protons are consumed by the preferential removal of each Mg from forsterite. These observations are interpreted to stem from the creation of additional ‘internal’ adsorption sites by the preferential removal of divalent metal cations which can be coupled to the condensation of partially detached Si. Similarly, Na and Al are preferentially removed from the albite surface at 2 > pH > 11; mass balance calculations suggest that three protons are consumed by the preferential removal of each Al atom from this surface over this entire pH range. Electrokinetic measurements on fresh mineral powders yield an isoelectric point (pHIEP) 2.6, 4.4, 3.0, 4.5, and <1, for wollastonite, diopside, enstatite, forsterite, and albite, respectively, consistent with the predominance of SiO2 in the surface layer of all of these multi-oxide silicates at acidic pH. Taken together, these observations suggest fundamental differences between the surface chemistry of simple versus multi-oxide minerals including (1) a dependency of the number and identity of multi-oxide silicate surface sites on the aqueous solution composition, and (2) the dominant role of metal-proton exchange reactions on the reactivity of multi-oxide mineral surfaces including their dissolution rate variation with aqueous solution composition.  相似文献   
84.
U-Pb age and isotope-geochemical features were determined for zircon from kyanite gneisses and amphibolites of the Chupa Sequence of the Belomorian mobile belt (BMB) of the Fennoscandian shield. The cores of the zircon from the gneisses marks the Neoarchean events within 2700–2800 Ma known in the BMB, while those of the amphibolites correspond to the age of magmatic crystallization (2775 ± 12 Ma). The inner rims of zircon from the amphibolites and gneisses likely record two different Neoarchean metamorphic events (2650 ± 8 and 2599 ± 10 Ma, respectively). The outer rims record Paleoproterozoic metamorphism with an age of 1890 Ma, which formed the modern appearance and mineral assemblages of the rock association. The value of δ18O in the zircon from the gneiss is 8.6‰ in cores, slightly decreases to 8.0‰ in inner rims, and sharply decreases to 3.9‰ in outer rims. The value of δ18O in the zircon from the amphibolite is around 6.2‰ in cores, increases up to 8.6 in inner rims, and decreases to 5.2‰ in outer rims. A significant decrease of δ18O is likely related to the anomalous composition of Svecofennian metamorphic fluid restricted to local shear zones. The geochemical features of the zircons in combination with their morphology and anatomy make it possible to distinguish zircon generations of different age and change in metamorphic environments.  相似文献   
85.
It is sometimes assumed that steric sea-level variations do not produce a gravity signal as no net mass change, thus no change of ocean bottom pressure is associated with it. Analyzing the output of two CO2 emission scenarios over a period of 2000 years in terms of steric sea-level changes, we try to quantify the gravitational effect of steric sea-level variations. The first scenario, computed with version 2.6 of the Earth System Climate Model developed at the University of Victoria, Canada (UVic ESCM), is implemented with a linear CO2 increase of 1% of the initial concentration of 365 ppm and shows a globally averaged steric effect of 5.2 m after 2000 years. In the second scenario, computed with UVic ESCM version 2.7, the CO2 concentration increases quasi-exponentially to a level of 3011 ppm and is hold fixed afterwards. The corresponding globally averaged steric effect in the first 2000 years is 2.3 m. We show, due to the (vertical) redistribution of ocean water masses (expansion or contraction), the steric effect results also in a small change in the Earth’s gravity field compared to usually larger changes associated with net mass changes. Maximum effects for computation points located on the initial ocean surface can be found in scenario 1, with the effect on gravitational attraction and potential ranging from 0.0 to −0.7·10−5 m s−2 and −3·10−3 to 6·10−3 m2 s−2, respectively. As expected, the effect is not zero but negligible for practical applications.  相似文献   
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The Pannonian Basin, originating during the Early Miocene, is a large extensional basin incorporated between Alpine, Carpathian and Dinaride fold-thrust belts. Back-arc extensional tectonics triggered deposition of up to 500-m-thick continental fluvio-lacustrine deposits distributed in numerous sub-basins of the Southern Pannonian Basin. Extensive andesitic and dacitic volcanism accompanied the syn-rift deposition and caused a number of pyroclastic intercalations. Here, we analyze two volcanic ash layers located at the base and top of the continental series. The lowermost ash from Mt. Kalnik yielded an 40Ar/39Ar age of 18.07?±?0.07?Ma. This indicates that the marine-continental transition in the Slovenia-Zagorje Basin, coinciding with the onset of rifting tectonics in the Southern Pannonian Basin, occurs roughly at the Eggenburgian/Ottnangian boundary of the regional Paratethys time scale. This age proves the synchronicity of initial rifting in the Southern Pannonian Basin with the beginning of sedimentation in the Dinaride Lake System. Beside geodynamic evolution, the two regions also share a biotic evolutionary history: both belong to the same ecoregion, which we designate here as the Illyrian Bioprovince. The youngest volcanic ash level is sampled at the Glina and Karlovac sub-depressions, and both sites yield the same 40Ar/39Ar age of 15.91?±?0.06 and 16.03?±?0.06?Ma, respectively. This indicates that lacustrine sedimentation in the Southern Pannonian Basin continued at least until the earliest Badenian. The present results provide not only important bench marks on duration of initial synrift in the Pannonian Basin System, but also deliver substantial backbone data for paleogeographic reconstructions in Central and Southeastern Europe around the Early–Middle Miocene transition.  相似文献   
89.
正1 Introduction It is known that more than 300 lakes and lagoons are present in the Crimean Peninsula,which are divided depending on position to 7 groups:Perekop,Tarkhankut,Evpatoriyskaya,Khersonesskaya,lake on the mountainpastures,Kerch and Genicheskaya.Almost the all lakes,with the exception of the small freshwater lakes,which situated on mountain pastures of the Main ridge of  相似文献   
90.
We review petrologic observations of reaction textures from high-grade rocks that suggest the passage of fluids with variable alkali activities. Development of these reaction textures is accompanied by regular compositional variations in plagioclase, pyroxenes, biotite, amphibole and garnet. The textures are interpreted in terms of exchange and net-transfer reactions controlled by the K and Na activities in the fluids. On the regional scale, these reactions operate in granitized, charnockitized, syenitized etc. shear zones within high-grade complexes. Thermodynamic calculations in simple chemical systems show that changes in mineral assemblages, including the transition from the hydrous to the anhydrous ones, may occur at constant pressure and temperature due only to variations in the H2O and the alkali activities. A simple procedure for estimating the activity of the two major alkali oxides, K2O and Na2O, is imple- mented in the TWQ software. Examples of calculations are presented for well-documented dehydration zones from South Africa, southern India, and Sri Lanka. The calculations have revealed two end-member regimes of alkalis during specific metamorphic processes: rock buffered, which is characteristic for the precursor rocks containing two feldspars, and fluid-buffered for the precursor rocks without K-feldspar. The observed reaction textures and the results of thermodynamic modeling are compared with the results of available experimental studies on the interaction of the alkali chloride and carbonate-bearing fluids with metamorphic rocks at mid-crustal conditions. The experiments show the complex effect of alkali activities in the fluid phase on the mineral assemblages. Both thermodynamic calculations and experiments closely reproduce paragenetic relations theoretically predicted by D.S. Korzhinskii in the 1940s.  相似文献   
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