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We document phyllosilicates occurrence along five shallow (exhumed from depths < 3 km) carbonate-hosted extensional faults from the seismically-active domain of the central Apennines, Italy. The shallow portion of this domain is characterized by a sedimentary succession consisting of ∼5–6 km thick massive carbonate deposits overlain by ∼2 km thick phyllosilicate-rich deposits (marls and siliciclastic sandstones). We show that the phyllosilicates observed within the studied carbonate-hosted faults derived from the overlying phyllosilicate-rich sedimentary deposits and were involved in the faulting processes. We infer that, during fault zone evolution, the phyllosilicates downward injected into pull-aparts (i.e., dilational jogs) that were generated along staircase extensional faults. With further displacement accumulation, the clayey material was smeared and concentrated into localized layers along the carbonate-hosted fault surfaces. These layers are usually thin (a few centimeters to decimeters thick), but can reach also a few meters in thickness. We suggest that, even in tectonic settings dominated by high frictional strength rocks (e.g., carbonates), localized layers enriched in weak phyllosilicates can occur along shallow fault surfaces thus reducing the expected fault strength during earthquakes, possibly promoting co-seismic slip propagation up to the Earth's surface. 相似文献
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为探索断层岩石摩擦特性对于断层力学性质的影响,我们采集了龙门山汶茂断裂韧性剪切带中的富含层状硅酸盐矿物的糜棱岩样品进行了水热条件下摩擦滑动实验研究.实验在三轴压机之上完成,实验温度为100~600℃,有效正压力100MPa,孔隙水压分别为30MPa和130MPa.为获得摩擦滑动的稳定性参数(a-b),剪切滑移速率在1.22μm·s-1,0.244μm·s-1和0.0488μm·s-1之间切换.实验发现在200~500℃的温度范围内,摩擦系数随着温度的增加而显著增大(约0.56~0.72).在200~300℃范围内,随温度的升高糜棱岩的摩擦滑动表现出由稳定的速度强化向不稳定速度弱化转变的趋势.在有效正压力不变的情况下,孔隙水压的增大会促进糜棱岩的摩擦滑动在500~600℃温度范围内由不稳定的速度弱化向稳定的速度强化的转变.实验给出的断层在原地深度处的脆性和塑性变形机制的转变,有助于理解断层深部的地震成核机制以及成核的温压条件. 相似文献
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S. Rakić V. Kahlenberg C. Weidenthaler B. Zibrowius 《Physics and Chemistry of Minerals》2002,29(7):477-484
Single crystals of C–Na2Si2O5 have been synthesized from the hydrothermal recrystallization of a glass. The title compound is monoclinic, space group P21/c with Z= 8 and unit-cell parameters a= 4.8521 (4)Å, b=23.9793(16)Å, c=8.1410(6)Å, β=90.15(1)° and V=947.2(2)Å3. The structure has been determined by direct methods and belongs to the group of phyllosilicates. It is based on layers of tetrahedra with elliptically six-membered rings in chair conformation. The sequence of directedness within a single ring is UDUDUD. The sheets are parallel to (010) with linking sodium cations in five- and sixfold coordination. Concerning the shape and the conformation of the rings, C–Na2Si2O5 is closely related to β-Na2Si2O5. However, both structures differ in the stacking sequences of the layers. A possible explanation for the frequently observed polysynthetic twinning of phase C is presented. In the 29Si MAS-NMR spectrum of C–Na2Si2O5 four well-resolved lines of equal intensity are observed at ?86.0, ?86.3, ?87.4, and ?88.2?ppm. The narrow range of isotropic chemical shifts reflects the great similarity of the environments of the different Si sites. This lack of pronounced differences in geometry renders a reliable assignment of the resonance lines to the individual sites on the basis of known empiric correlations and geometrical features impossible. 相似文献
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