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The stability analysis of curved earth retaining walls, stabilized by reinforcing membranes, is investigated by means of a multiphase model developed in the framework of the yield design approach. This model is an extension of that previously developed for soils reinforced by linear inclusions. It combines the advantage of a homogenization approach in terms of improved computational efficiency, with its capability to account for a specific soil–reinforcement failure condition, in a rational and systematic way. Application of this model is performed on the illustrative example of a cylindrical‐reinforced retaining wall by means of the kinematic approach of yield design, which provides upper bound estimates for the retaining wall stability factor. Nondimensional charts are finally presented assessing the influence of relevant parameters such as the curvature of the wall, the length of the reinforcing membranes or the reinforcement pull‐out resistance. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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人地关系调控与生态环境 --以长江洪灾为例 总被引:5,自引:0,他引:5
以长江洪灾为例,分析了人地相互作用的内容与方式,人地关系系统调控的任务与措施。认为洪灾频发的重要原因是人类对地质资源的不合理开发利用而导致生态系统的严重破坏。并认为要培植生态系统的抗干扰能力,应及时调整人地关系,改善农村的经济方式与经济条件,把生态建设作为国家长治久安的根本大事长期坚持下去。 相似文献
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AN ATMOSPHERIC MOTION EQUATION BUILT ON THE CONSERVATIVE RELATIONSHIP OF THE ANGULAR MOMENTUM EXCHANGE BETWEEN THE SOLID EARTH AND THE ATMOSPHERE ON SEASONAL-ANNUAL TIMESCALE
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Within the seasonal-annual timeseale,there exists an angular momentum conservative exchange relationship be-tween the solid earth and the atmosphere,and their angular momentum exchange not only can cause variations inlength-of-day(LOD)but also can express anomalies in atmospheric general circulation.Therefore,their angular mo-mentum exchange mechanism should be introduced into the general circulation model.Considering the angular momentum anomalous exchange caused by the air-earth interface friction effect,awhole-layer atmospheric motion equation is derived in this paper including the earth spin anomalous friction forceparameterized by using the change in the earth rotation rate.Through analysing the equation,it shows that the magni-tude of the earth spin anomalous friction force is the same as that of Coriolis force on seasonal-annual timescale. 相似文献
899.
运用相对运动的地球动力学理论,把软流圈以上的岩石圈和软流圈以下的地球内圈,作为两个独立的运动单元来考察它们随地球自转时所发生的变化和各自的运动状态。完整的岩石圈碎裂成岩石块之后,它们各自作为独立的单元,在纬向西漂力、经向离极力和洋底扩张力联合作用下,产生相对运动。 相似文献
900.
The aquatic chemistry of rare earth elements in rivers and estuaries 总被引:17,自引:0,他引:17
Edward R. Sholkovitz 《Aquatic Geochemistry》1995,1(1):1-34
Laboratory experiments were carried out to determine how pH, colloids and salinity control the fractionation of rare earth elements (REEs) in river and estuarine waters. By using natural waters as the reaction media (river water from the Connecticut, Hudson and Mississippi Rivers) geochemical reactions can be studied in isolation from the large temporal and spatial variability inherent in river and estuarine chemistry. Experiments, field studies and chemical models form a consistent picture whereby REE fractionation is controlled by surface/solution reactions. The concentration and fractionation of REEs dissolved in river waters are highly pH dependent. Higher pH results in lower concentrations and more fractionated composition relative to the crustal abundance. With increasing pH the order of REE adsorption onto river particle surfaces is LREEs > MREEs > HREEs. With decreasing pH, REEs are released from surfaces in the same order. Within the dissolved (<0.22 µm) pool of river waters, Fe-organic colloids are major carriers of REEs. Filtration through filters and ultrafilters with progressively finer pore sizes results in filtrates which are lower in absolute concentrations and more fractionated. The order of fractionation with respect to shale, HREEs > MREEs > LREEs, is most pronounced in the solution pool, defined here as <5K and <50K ultrafiltrates. Colloidal particles have shale-like REE compositions and are highly LREE enriched relative to the REE composition of the dissolved and solution pools. The addition of sea water to river water causes the coagulation of colloidal REEs within the dissolved pool. Fractionation accompanies coagulation with the order of sea water-induced removal being LREEs > MREEs > HREEs. While the large scale removal of dissolved river REEs in estuaries is well established, the release of dissolved REEs off river particles is a less studied process. Laboratory experiments show that there is both release and fractionation of REEs when river particles are leached with seawater. The order of sea water-induced release of dissolved REE(III) (LREEs > MREEs > HREEs) from Connecticut River particles is the same as that associated with lowering the pH and the same as that associated with colloidal particles. River waters, stripped of their colloidal particles by coagulation in estuaries, have highly evolved REE composition. That is, the solution pool of REEs in river waters are strongly HREE-enriched and are fractionated to the same extent as that of Atlantic surface seawater. This strengthens the conclusions of previous studies that the evolved REE composition of sea water is coupled to chemical weathering on the continents and reactions in estuaries. Moreover, the release of dissolved Nd from river particles to sea water may help to reconcile the incompatibility between the long oceanic residence times of Nd (7100 yr) and the inter-ocean variations of the Nd isotopic composition of sea water. Using new data on dissolved and particle phases of the Amazon and Mississippi Rivers, a comparison of field and laboratory experiments highlights key features of REE fractionation in major river systems. The dissolved pool of both rivers is highly fractionated (HREE enriched) with respect to the REE composition of their suspended particles. In addition, the dissolved pool of the Mississippi River has a large negative Ce-anomaly suggesting in-situ oxidation of Ce(III). One intriguing feature is the well developed maximum in the middle REE sector of the shale normalized patterns for the dissolved pool of Amazon River water. This feature might reflect competition between surface adsorption and solution complexation with carbonate and phosphate anions. 相似文献