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1.
A study of polytypism in synthetic polycrystalline pseudowollastonite has been made using conventional and high resolution transmission electron microscopy (TEM and HRTEM). Three polytypes of 2, 4 and 6-layers coexist in the one sample in the form of lamellae parallel to (001). From the electron microscopy images the lamellae are interpreted as combinations of the stacking fault vectors: 1/3 [010], 1/6 [310] and 1/6 [3 $\bar 1$ 0], which are probably all equivalent at high temperatures. The polytype lamellae are stable even after prolonged annealing at high temperatures greater than 1700K. These observations suggest that the most frequently reported 4-layer polytype is not the only high-temperature stable polytype. No evidence of melt is detected in samples annealed in the regime where premelting behaviour of pseudowollastonite has previously been reported (above 1600 K).  相似文献   
2.
A study of Ca self-diffusion along the b axis in synthetic (iron free) diopside single crystal was performed at temperatures ranging from 1273 K to 1653 K. Diffusion profiles of 44Ca were measured using α-particles Rutherford Backscattering (α-RBS) micro analysis. We unambiguously find two distinct diffusional regimes, characterized by activation enthalpies H = 280 ± 26 kJ/mol and H = 951 ± 87 kJ/mol at temperatures lower and upper than 1515 K, respectively. This change of diffusion regime takes place near the onset of premelting as detected in calorimetric measurements and can be interpreted in terms of enhanced formation of Frenkel point defects with an activation enthalpy of formation of 1524 ± 266 kJ/mol (H f/2 = 762 kJ/mol), in accordance with our high-temperature diffusion data. If premelting of diopside is actually related to Ca-Frenkel point defect concentration, this concentration could reach up to few mole percents close to the melting temperature.  相似文献   
3.
Atransmission electron microscope (TEM) study of quartz-coesite inclusions in garnet in crustal rocks from the Western Alps is presented. Coesite shows a low dislocation density (<107 cm?2), and quartz a higher density of defects, Brasil twins (104 cm?1) and dislocations (108 cm?2). It is concluded that coesite has been not or only slightly plastically deformed and that the yield strength of coesite is higher than that of quartz. The large scale deformation implications are briefly discussed. TEM observations show no systematic topotactic relationship between the two polymorphs and their boundaries have a scalloped morphology which suggests that growth of quartz from coesite was controlled by a diffusion process.  相似文献   
4.
In order to better identify the mineral phase which controls the rheology of the transition zone (between 410 and 660 km depth) transmission electron microscopy observations were made on several coexisting spinel-garnet assemblies: alkremite xenolith; pyrope-rich – MgO:1.1Al2O3 spinel assembly deformed at 1173K, 800 MPa in a Griggs apparatus; (Mg,Fe)3(Al,Mg,Si)2Si3O12 majorite – (Mg,Fe)2SiO4 spinel assembly synthesized in a laser heated diamond anvil cell. It was found that garnet crystals systematically remain undeformed while spinel crystals are plastically deformed. These results are in accord with the assumption that the rheology of majorite is stronger than the rheology of spinel, in the conditions of the transition zone.  相似文献   
5.
A numerical study demonstrates the effects of flooding on subsurface hydrological flowpaths and nitrate removal in anoxic groundwater in riparian zones with a top peat layer. A series of two-dimensional numerical simulations with changing conditions for flow (steady state or transient with flooding), hydrogeology, denitrification, and duration of flooding demonstrate how flowpaths, residence times, and nitrate removal are affected. In periods with no flooding groundwater flows horizontally and discharges to the river through the riverbed. During periods with flooding, shallow groundwater is forced upwards as discharge through peat layers that often have more optimal conditions for denitrification caused by the presence of highly reactive organic matter. The contrast in hydraulic conductivity between the sand aquifer and the overlying peat layer, as well as the flooding duration, have a significant role in determining the degree of nitrate removal.  相似文献   
6.
7.
Coesite has been found in a metasedimentary rock in a continental unit of the Western Alps (Dora Maira massif). The rock preserves the high-pressure, low-temperature assemblage of nearly pure pyrope-talc-phengite-kyanite in a quartz matrix; coesite exclusively occurs as inclusions in pyrope and is partly inverted to quartz. Textural observations and mechanical considerations suggest that the rock crystallised in the coesite stability field. A simple elastic model for a coesite inclusion in pyrope explains why coesite has been exclusively preserved in the inclusions and not in the matrix. Combined with petrological data the model constrains the crystallisation conditions of the pyrope-coesite rock (P > 28kbar, 650 < T < 830°C) and possible uplift paths. The paths derived suggest a mechanism of rapid decompression without any temperature increase, which must be related to tectonic processes.

This finding has an important bearing on the significance of P-T conditions estimated from minerals occurring as inclusions and on the actual behaviour of continental crust in collision zones.  相似文献   

8.
The classical solid-medium apparatus (Griggs apparatus) is generally viewed as a machine of poor accuracy with a large amount of uncertainty. However, a new generation of equipment with new assemblies and experimental procedures has greatly enhanced the capability of the apparatus. Experiments performed on the apparatus set up in our Laboratory on T-oriented Yule Marble samples show that the yield strength of material can be measured with reasonable precision (within 10 MPa) and a yield strength as low as 50 MPa can be detected. The apparatus is particularly adapted to work on small specimens e.g. single crystals a few millimetres in size.  相似文献   
9.
Peridotite xenoliths with a broad range of textures provides evidence for consistent microstructural evolution in a vertical transect of the shallow lithospheric mantle (35–55 km depth) beneath the Persani Mountains, SE Carpathians, Romania, due to ongoing plate convergence in the Carpathian Arc nearby. The recrystallized grain size, crystal preferred orientations strength, and resulting seismic anisotropy vary continuously and display a strong correlation to equilibrium temperatures, suggesting a continuous change in deformation conditions with depth. The shallowmost xenoliths have microstructures typical of high stress deformation, marked by strong recrystallization to fine grain sizes, which results in weak crystal preferred orientations and anisotropy. The deepest xenoliths have coarse-grained porphyroclastic microstructures and strong crystal preferred orientations. Replacive orthopyroxene structures, consuming olivine, and high H2O concentrations in the pyroxenes are observed in some xenoliths indicating limited percolation of fluids or volatile-rich melts. Despite the high stress deformation and high H2O contents in some of the studied xenoliths, analysis of olivine crystallographic orientations indicates that [100] slip systems, rather than “wet” [001] accommodate most of the deformation in all samples. Seismic anisotropy estimated from the measured olivine and pyroxene crystal preferred orientations suggests that the strike-parallel fast SKS polarization directions and ~ 1 s delay times measured in the SE Carpathians are likely the consequence of convergence-driven belt-parallel flow in the lithospheric mantle.  相似文献   
10.
We performed in situ infrared spectroscopic measurements of OH bands in a forsterite single crystal between ?194 and 200 °C. The crystal was synthesized at 2 GPa from a cooling experiment performed between 1,400 and 1,275 °C at a rate of 1 °C per hour under high silica-activity conditions. Twenty-four individual bands were identified at low temperature. Three different groups can be distinguished: (1) Most of the OH bands between 3,300 and 3,650 cm?1 display a small frequency lowering (<4 cm?1) and a moderate broadening (<10 cm?1) as temperature is increased from ?194 to 200 °C. The behaviour of these bands is compatible with weakly H-bonded OH groups associated with hydrogen substitution into silicon tetrahedra; (2) In the same frequency range, two bands at 3,617 and 3,566 cm?1 display a significantly anharmonic behaviour with stronger frequency lowering (42 and 27 cm?1 respectively) and broadening (~30 cm?1) with increasing temperature. It is tentatively proposed that the defects responsible for these OH bands correspond to H atoms in interstitial position; (3) In the frequency region between 3,300 and 3,000 cm?1, three broad bands are identified at 3,151, 3,178 and 3,217 cm?1, at ?194 °C. They exhibit significant frequency increase (~20 cm?1) and broadening (~70 cm?1) with increasing temperature, indicating moderate H bonding. These bands are compatible with (2H)Mg defects. A survey of published spectra of forsterite samples synthesized above 5 GPa shows that about 75 % of the incorporated hydrogen belongs to type (1) OH bands associated with Si substitution and 25 % to the broad band at 3,566 cm?1 (type (2); 3,550 cm?1 at room temperature). The contribution of OH bands of type (3), associated to (2H)Mg defects, is negligible. Therefore, solubility of hydrogen in forsterite (and natural olivine compositions) cannot be described by a single solubility law, but by the combination of at least two laws, with different activation volumes and water fugacity exponents.  相似文献   
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