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1.
We propose a new runoff model including an outflow process that was applied to two adjacent basins (CL, TL) located in Lambir Hills National Park in north‐central Sarawak, Malaysia. Rainfall, runoff, topography, and soil layer thickness were observed. About 19% of annual runoff was observed in the CL basin (21.97 ha), whereas about 46% was observed in the TL basin (23.25 ha). It was inferred that the CL basin has an outflow because of low base flow, small runoff peak, and excessive water loss. By incorporating the outflow process into the HYdrological CYcle MODEL, good agreement between the data generated by the model and that observed was shown, with the exception of the data from the rainless period. Then, the fitting parameters for each basin were exchanged, except for the outflow parameter, and the characteristics of each basin were compared by calculating virtual runoff. As a result, the low base flow of the CL basin was estimated by the movement of the rainwater that escaped from the basin as deep percolation or lateral flow (11% of rainfall). The potential of the CL basin for mitigating flood and drought appeared to be higher than that of the TL basin. This is consistent with the topographic characteristics of the CL basin, which has a gentler slope than the TL basin. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
2.
Boninite is an unusual, plagioclase-free magnesian andesite, occurring as vesicular pillow lavas and hyaloclastites, accompanied by andesites and dacites in Chichi-jima, Bonin Islands. The Bonin Islands belong to the Izu-Mariana arc and consist of dominant volcanic rocks and subordinate sedimentary rocks of late Oligocene-early Miocene age. The chemistry of boninite is characterized by high contents of MgO. Cr and Ni similar to primitive basalts, but apparently in ill accord with its relatively high SiO2 content of ? 55%. The relation of SiO2 to total FeO/MgO ratio indicates that boninite belongs to the cale-alkalic rock suite. The mineralogy of boninite consists of olivine (Fo87-90), orthopyroxene (En87-90), clinopyroxene (Wo38-35En37-44Fs25-21), hydrous glass and Cr-spinel, Experimental studies show that the magma of boninite composition could be in equilibrium with upper mantle peridotite at pressures less than 17 kb and temperatures of 1200–1050°C under high PH2O. It is suggested that boninite is a sea-floor quenched product (900°C) of a direct partial melt of the upper mantle. Related andesites and dacites are considered to be probably fractional crystallization products from the same magma.  相似文献   
3.
An unusual association of chromite and hornblende was found in the spessartites of andesite composition, occurring as a dike swarm associated with a Cretaceous granite batholith. The spessartites are largely porphyritic with phenocrysts of either hornblende or augite. One dike, comprising a finegrained spessartite, exhibits distinct chilled selvages of aphanitic facies. The chromites in the fine-grained and augite-spessartites are significantly higher in Cr/ (Cr+Al) than those occurring rarely as inclusions in the phenocrystic hornblendes in the hornblende spessartite, although both are similar in Mg/ (Mg+Fe), Fe2O3, and TiO2. The phenocrystic hornblendes are titaniferous pargasite with high Mg/ (Mg+Fe), and differ in their higher octahedral Al from the groundmass hornblendes including those in the fine-grained spessartite. The crystallization sequence in the phenocrystic hornblende-bearing spessartites is Al-rich chromite, phenocrystic hornblende, and plagioclase without pyroxene, suggesting a high water content in the magma and the start of the crystallization at relatively high pressures. The finegrained spessartite from which the porphyritic spessartites have been derived by fractionation of dominant mafic minerals, has the high Mg-value and Cr content equivalent to those in primitive, undifferentiated basalts, although still andesitic in SiO2 content. Chemically similar magnesian andesites, although uncommon, found in some orogenic calc-alkalic suites may represent a magma composition in equilibrium with mantle peridotite under the condition of high water pressures.  相似文献   
4.
High-Mg diorites that have similar whole rock composition to high-Mg andesites (HMAs) should not be simply interpreted as rocks solidified from the HMA magmas, because the high-Mg diorites may be mafic cumulates derived from a different magma from the HMAs.

The HMAs contain unique clinopyroxenes with higher Mg# and Si than those of other sub-alkaline series igneous rocks. The Mg# and Si are controlled by the source magma composition rather than its crystallized conditions such as pressure and temperature. The chemical composition of clinopyroxenes would present important information for the investigation of the source of high-Mg diorites.

We considered the source of Early Cretaceous high-Mg diorites on Kyushu Island, southwest Japan arc, based on their clinopyroxene and whole rock compositions. The clinopyroxenes have similar chemical characteristics to those in HMAs rather than those in other sub-alkaline rocks. Moreover, the whole rock compositions are equivalent to the sanukitic HMA and do not show features of mafic cumulates. This indicates that the high-Mg diorites solidified from sanukitic HMA magmas. It is generally believed that the sanukitic HMA magmas involve the subduction of a young and/or hot oceanic slab was situated in their genesis. Therefore, the occurrence of the high-Mg diorites suggests that Kyushu was situated in the tectonic setting of young and/or hot slab subduction in the Early Cretaceous.  相似文献   

5.
Experiments on the hydrogenation of CO on pure CO and CO-H2O mixed ice have been performed at temperatures between 8 and 20 K. We obtained temperature and compositional dependence of the effective reaction rate constants. Results indicate that hydrogenation proceeds efficiently on pure solid CO and CO-H2O mixed ice at temperatures below 10 and 20 K, respectively. Rate constants for pure CO decreased significantly at 12 K compared to those obtained with CO-H2O mixed ice. Hydrogenation of CO at temperatures greater than 12 K were catalyzed by the H2O adjacent to the CO. The importance of the experimental results for some relevant astrophysical environments has also been outlined.  相似文献   
6.
Atomic force microscopy (AFM) was used to study the rates of migration of the (10¯1 4) plane of a single-crystal of calcite dissolving in 0.1 M NaCl aqueous solutions at room temperature. The solution pH and PCO 2 controlled in the ranges 4.4 < pH < 12.2 and 0 < PCO 2 < 10-3.5 atm (ambient), respectively. Measured step velocities were compared with the mineral dissolution rates determined from the calcium fluxes. The step velocity is defined as the average of the velocities of the obtuse and acute steps. Rates of step motion increased gradually from 1.4(±0.2) at pH 5.3 to 2.4(±0.3) nm s-1 at pH 8.2, whereas the rates inverted and decreased to the minimum value of 0.69(±0.18) nm s-1 at pH 10.8. For pH > 10.8, only the velocity of the obtuse steps increased as pH increased, whereas that of acute steps gradually decreased.The dissolution rate of the mineral can be calculated from the measured step velocities and average slope, which is proportional to the concentration of exposed monomolecular steps on the surface. The average slope of the dissolving mineral, measured at pH 5.6 and 9.7, was 0.026 (±0.015). Using this slope, we calculate bulk dissolution rates for 5.3 < pH < 12.2 of 4.9(±3.0) × 10-11 to 1.8(±1.0) × 10-10 mol cm-2 s-1. The obtained dissolution rate can be expressed by the following empirical equation:Rdss = 10-4.66(±0.13)[H+] + 10-3.87(±0.06)[HCO3 -] + 10-7.99(plusmn; 0.08)[OH-]We propose that calcite dissolution in these solutions is controlled by elementary reactions that are similar to those that control the dissolution of other amphoteric solids, such as oxides. The mechanisms include the proton-enhanced hydration and detachment of calcium-carbonate ion pairs. The detachments are enhanced by the presence of adsorbed nucleophiles, such as hydroxyl and bicarbonate ions, and by protons adsorbed to key oxygens. A molecular model is proposed that illustrates these processes.  相似文献   
7.
Numerical modeling of a semienclosed narrow channel demonstrates the dynamical dependency of an estuarine residual circulation (ERC) on tidal amplitudes. The ERC is defined by tidally-averaged current field. The tidally-averaged fields show that the ERC-strength variation is classified into highly stratified, partially stratified and weakly stratified ranges, respectively. The ERC becomes weaker as the tidal amplitude (and hence vertical mixing) increases in the highly and weakly stratified ranges. However, the ERC becomes stronger oppositely in the partially stratified range. The nonlinear forces induced by tides significantly affect the ERC as well as the pressure gradient force due to the freshwater flux and the vertical stress divergence (vertical eddy viscous force). In particular, the tidal stress and tidally-oscillating component of vertical stress divergence are quite important in ERC dynamics. The latter causes the enhancement of ERC in proportion to the vertical mixing in the partially stratified range.  相似文献   
8.
Petrological evolution of the Tertiary island arc in the Izu-Mariana region has been accompanied by the development of three different volcanic suites: 1) oceanridge basalt now exposed as the metamorphic basement on Yap; 2) island-arc tholeiites of Eocene to early Oligocene age characterized by low contents of incompatible elements at all levels of silica enrichment; and 3) calc-alkalic rocks of late Oligocene to early Miocene age showing higher contents of silica and incompatible elements. All these three suites have primitive, undifferentiated basalts or andesites (boninites) characterized by high Mg/Fe, Cr, and Ni, suggesting that they have been derived from an upper mantle peridotite at relatively high temperatures. The earliest volcanism appears to have occurred at a spreading ridge. Later, as subduction proceeded, the island-arc tholeiite magma may have been produced by the introduction of a smaller amount of water into the locus of fusion from the subducted oceanic crust. An increasingly larger amount of water introduced into the same region could have led to the development of the more siliceous, calc-alkalic magma, as represented typically by the boninite.  相似文献   
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