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11.
The accuracy of the computed stress distribution near the free surface of vertical slopes was evaluated in this study as a function of the element size, including aspect ratio. To accomplish this objective, a parametric study was carried out comparing stresses computed using the finite element method (FEM) to those obtained from a physical model composed of photoelastic material. The results of the study indicate a reasonable agreement between a gelatin model and the FEM model for shear stresses, and an overall good agreement between the two models for the principal stresses. For stresses along the top of the slope, the height of the element tends to be more important than width or aspect ratio, at least for aspect ratios up to 4. In all cases, the greatest difference between the two models occurs in the vicinity of the slope. Specifically, if H is defined as the slope height, an element height of H/10 appears to be adequate for the study of stresses deep within the slope, such as for typical embankment analyses. However, for cases where tensile stresses in the vicinity of the slope face which are critical, such as for the stability analysis of steep slopes, element heights as small as H/32, or higher‐order elements, are necessary. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
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Abstract— Primary minerals in calcium‐aluminum‐rich inclusions (CAIs), Al‐rich and ferromagnesian chondrules in each chondrite group have δ18O values that typically range from ?50 to +5%0. Neglecting effects due to minor mass fractionations, the oxygen isotopic data for each chondrite group and for micrometeorites define lines on the three‐isotope plot with slopes of 1.01 ± 0.06 and intercepts of ?2 ± 1. This suggests that the same kind of nebular process produced the 16O variations among chondrules and CAIs in all groups. Chemical and isotopic properties of some CAIs and chondrules strongly suggest that they formed from solar nebula condensates. This is incompatible with the existing two‐component model for oxygen isotopes in which chondrules and CAIs were derived from heated and melted 16O‐rich presolar dust that exchanged oxygen with 16O‐poor nebular gas. Some FUN CAIs (inclusions with isotope anomalies due to fractionation and unknown nuclear effects) have chemical and isotopic compositions indicating they are evaporative residues of presolar material, which is incompatible with 16O fractionation during mass‐independent gas phase reactions in the solar nebula. There is only one plausible reason why solar nebula condensates and evaporative residues of presolar materials are both enriched in 16O. Condensation must have occurred in a nebular region where the oxygen was largely derived from evaporated 16O‐rich dust. A simple model suggests that dust was enriched (or gas was depleted) relative to cosmic proportions by factors of ~10 to >50 prior to condensation for most CAIs and factors of 1–5 for chondrule precursor material. We infer that dust‐gas fractionation prior to evaporation and condensation was more important in establishing the oxygen isotopic composition of CAIs and chondrules than any subsequent exchange with nebular gases. Dust‐gas fractionation may have occurred near the inner edge of the disk where nebular gases accreted into the protosun and Shu and colleagues suggest that CAIs formed. 相似文献
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Scott M. MCLENNAN 《Meteoritics & planetary science》2003,38(6):895-904
Abstract— Basaltic shergottites display a systematic decrease in K/Th, K/U, and K/La ratios with increasing K content. These trends are interpreted as mixing lines between relatively young martian magmas derived from highly depleted mantle sources and an ancient large‐ion lithophile (LIL) element‐enriched crustal component. One implication of this is that a substantial fractionation of these ratios occurs during the early crustal differentiation on Mars. Isotopic evidence from SNC meteorites and compositional data from Pathfinder and orbital gamma ray spectroscopy suggest that in excess of 50% of the LIL element complement of Mars resides in the crustal reservoir. If so, the primitive mantle of Mars is significantly more volatile‐depleted (i.e., lower K/Th, K/U, K/La) than previously thought but probably (though not necessarily) still less volatile‐depleted than the primitive mantle of the Earth. The La/Th ratios of virtually all SNC meteorites are subchondritic, including those with the most severe LREE‐depletion. Extrapolation of the basaltic shergottite trend suggests that both the depleted mantle end member and the enriched crustal end member have subchondritic La/Th ratios. This is in contrast with the Earth where basalts from LIL element‐depleted sources such as MORB have superchondritic La/Th ratios, complementary to the subchondritic ratios of the continental crust. Accordingly, assuming that the refractory elements are in chondritic proportions for the Mars primitive mantle, an additional major geochemical reservoir must exist on Mars that may not yet have been sampled. 相似文献
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Methane, a potential biosignature, has recently been detected in the martian atmosphere. This Note focuses on field investigations/operational simulations and laboratory studies which resulted in successful detection of methane within arid terrestrial soils, as distinct from the usual methanogen environment, but in at least partial analogy to martian conditions. 相似文献
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R. Scott Anderson Renata B. Jass Jaime L. Toney Craig D. Allen Marcey Hess Julianna Fessenden 《Quaternary Research》2008,69(2):263-275
Chihuahueños Bog (2925 m) in the Jemez Mountains of northern New Mexico contains one of the few records of late-glacial and postglacial development of the mixed conifer forest in southwestern North America. The Chihuahueños Bog record extends to over 15,000 cal yr BP. An Artemisia steppe, then an open Picea woodland grew around a small pond until ca. 11,700 cal yr BP when Pinus ponderosa became established. C/N ratios, δ13C and δ15N values indicate both terrestrial and aquatic organic matter was incorporated into the sediment. Higher percentages of aquatic algae and elevated C/N ratios indicate higher lake levels at the opening of the Holocene, but a wetland developed subsequently as climate warmed. From ca. 8500 to 6400 cal yr BP the pond desiccated in what must have been the driest period of the Holocene there. C/N ratios declined to their lowest Holocene levels, indicating intense decomposition in the sediment. Wetter conditions returned after 6400 cal yr BP, with conversion of the site to a sedge bog as groundwater levels rose. Higher charcoal influx rates after 6400 cal yr BP probably result from greater biomass production rates. Only minor shifts in the overstory species occurred during the Holocene, suggesting that mixed conifer forest dominated throughout the record. 相似文献
18.
The Dead Sea Basin is the lowest point on earth and is tectonically subsiding. During the Holocene Period the climate became much drier with increasing evaporation whereby initially lacustrine sediments were deposited from the non-marine brines, giving a multi-layered stratigraphy of lime carbonate and halite sediments. The lime carbonate sediments are comprised of laminated, clay to silt sized, clastic sediments (calcite) and authigenic aragonite and gypsum. The halite commonly appears as rock salt. Chemical industries, based on harvesting the salts from the Dead Sea, have developed on both the Israeli and the Jordanian sides of the basin. The lime carbonate soils are used for dike construction, and these soils, together with significant salt layers, are encountered in the foundations of structures, dikes, and tailings dams, requiring definition of their geotechnical properties. Use of standard soil mechanics definitions and testing approaches for the lime carbonates have been found inapplicable, particularly in view of their exceptionally high saline content, and it has been necessary to develop new concepts. The rock salt is encountered at shallow depths, with unit weights considerably lower than those usually discussed in the literature, and with correspondingly different mechanical properties. The geotechnical properties of these soils, and approaches used to define them, are discussed in the paper. 相似文献
19.
Imad A.M. Ahmed Neil M.J. Crout Scott D. Young 《Geochimica et cosmochimica acta》2008,72(6):1498-1512
Time-dependent sorption and desorption of Cd on calcite was studied over 210 days utilizing 109Cd as a tracer to distinguish between ‘labile’ and ‘non-labile’ forms of sorbed Cd. Stabilizing the calcite suspensions for 12 months under atmospheric PCO2 and controlled temperature was necessary to reliably follow Cd dynamics following initial sorption. Results revealed time-dependant Cd sorption and marked desorption hysteresis by calcite under environmentally relevant conditions. Data obtained were fitted to a first-order kinetic model and a concentric shell diffusion model. Both models described the progressive transfer of Cd2+ to a less reactive form within calcite and subsequent desorption of Cd subject to different initial contact times. The kinetic model provided a better fit to the combined sorption and desorption data (R2 = 0.992). It differentiates between two ‘pools’ of sorbed Cd2+ on calcite, ‘labile’ and ‘non-labile’, in which labile sorbed Cd is in immediate equilibrium with the free Cd2+ ion activity in solution whereas non-labile Cd is kinetically restricted. For the diffusion model (R2 = 0.959), the rate constants describing Cd dynamics in calcite produced a half-life for Cd desorption of ∼175 d, for release to a ‘zero-sink’ solution. Results from this study allow comment on the likely mechanisms occurring at the calcite surface following long-term Cd sorption. 相似文献
20.
The current study provides an investigation of abiotic reduction of an oversaturated uranyl solution driven by iron nanoparticle oxidation. The reactivity of nano-scale zero-valent iron (ZVI) under mildly oxic conditions (1.2% O2 and 0.0017% CO2) was studied in 1000 ppm uranyl solution in the pH range 3-7, at reaction times from 10 min to 4 h. Reductive precipitation of UO2 was observed as the main process responsible for the removal of uranium from solution with the kinetics of reaction becoming increasingly favourable at higher pH. Despite working with an oversaturated uranium solution, the precipitation of UO2 occurred in preference to precipitation of UO3·2H2O (metaschoepite) at reaction times between 1 and 4 h and for uranyl solutions initially set up at pH ?5. Characterisation of both solid and solution phases was performed using X-ray photoelectron spectroscopy (XPS), focused ion beam (FIB) imaging, X-ray diffraction (XRD) and inductively coupled plasma atomic emission spectroscopy (ICP-AES). 相似文献