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111.
In this study, the simulation of an extreme weather event like heavy rainfall over Mumbai (India) on July 26, 2005 has been attempted with different horizontal resolutions using the Advanced Research Weather Research Forecast model version 2.0.1 developed at the National Center for Atmospheric Research (NCAR), USA. The study uses the Betts–Miller–Janjic (BMJ) and the Grell–Devenyi ensemble (GDE) cumulus parameterization schemes in single and nested domain configurations. The model performance was evaluated by examining the different predicted parameters like upper and lower level circulations, moisture, temperature, and rainfall. The large-scale circulation features, moisture, and temperature were compared with the National Centers for Environmental Prediction analyses. The rainfall prediction was assessed quantitatively by comparing rainfall from the Tropical Rainfall Measuring Mission products and the observed station values reported in the Indian Daily Weather Reports from India Meteorological Department (IMD). The quantitative validation of the simulated rainfall was done by calculating the categorical skill scores like frequency bias, threat scores (TS), and equitable threat scores (ETS). It is found that in all simulations, both in single and nested domains, the GDE scheme has outperformed the BMJ scheme for the simulation of rainfall for this specific event.  相似文献   
112.
Iron (III) oxides are ubiquitous in near-surface soils and sediments and interact strongly with dissolved phosphates via sorption, co-precipitation, mineral transformation and redox-cycling reactions. Iron oxide phases are thus, an important reservoir for dissolved phosphate, and phosphate bound to iron oxides may reflect dissolved phosphate sources as well as carry a history of the biogeochemical cycling of phosphorus (P). It has recently been demonstrated that dissolved inorganic phosphate (DIP) in rivers, lakes, estuaries and the open ocean can be used to distinguish different P sources and biological reaction pathways in the ratio of 18O/16O (δ18OP) in PO43−. Here we present results of experimental studies aimed at determining whether non-biological interactions between dissolved inorganic phosphate and solid iron oxides involve fractionation of oxygen isotopes in PO4. Determination of such fractionations is critical to any interpretation of δ18OP values of modern (e.g., hydrothermal iron oxide deposits, marine sediments, soils, groundwater systems) to ancient and extraterrestrial samples (e.g., BIF’s, Martian soils). Batch sorption experiments were performed using varied concentrations of synthetic ferrihydrite and isotopically-labeled dissolved ortho-phosphate at temperatures ranging from 4 to 95 °C. Mineral transformations and morphological changes were determined by X-Ray, Mössbauer spectroscopy and SEM image analyses.Our results show that isotopic fractionation between sorbed and aqueous phosphate occurs during the early phase of sorption with isotopically-light phosphate (P16O4) preferentially incorporated into sorbed/solid phases. This fractionation showed negligible temperature-dependence and gradually decreased as a result of O-isotope exchange between sorbed and aqueous-phase phosphate, to become insignificant at greater than ∼100 h of reaction. In high-temperature experiments, this exchange was very rapid resulting in negligible fractionation between sorbed and aqueous-phase phosphate at much shorter reaction times. Mineral transformation resulted in initial preferential desorption/loss of light phosphate (P16O4) to solution. However, the continual exchange between sorbed and aqueous PO4, concomitant with this mineralogical transformation resulted again in negligible fractionation between aqueous and sorbed PO4 at long reaction times (>2000 h). This finding is consistent with results obtained from natural marine samples. Therefore, 18O values of dissolved phosphate (DIP) in sea water may be preserved during its sorption to iron-oxide minerals such as hydrothermal plume particles, making marine iron oxides a potential new proxy for dissolved phosphate in the oceans.  相似文献   
113.
This study elucidates the characteristics of ambient PM2.5 (fine) and PM1 (submicron) samples collected between July 2009 and June 2010 in Raipur, India, in terms of water soluble ions, i.e. Na+, NH 4 + , K+, Mg2+, Ca2+, Cl?, NO 3 ? and SO 4 2? . The total number of PM2.5 and PM1 samples collected with eight stage cascade impactor was 120. Annual mean concentrations of PM2.5 and PM1 were 150.9?±?78.6 μg/m3 and 72.5?±?39.0 μg/m3, respectively. The higher particulate matter (PM) mass concentrations during the winter season are essentially due to the increase of biomass burning and temperature inversion. Out of above 8 ions, the most abundant ions were SO 4 2? , NO 3 ? and NH 4 + for both PM2.5 and PM1 aerosols; their average concentrations were 7.86?±?5.86 μg/m3, 3.12?±?2.63 μg/m3 and 1.94?±?1.28 μg/m3 for PM2.5, and 5.61?±?3.79 μg/m3, 1.81?±?1.21 μg/m3 and 1.26?±?0.88 μg/m3 for PM1, respectively. The major secondary species SO 4 2? , NO 3 ? and NH 4 + accounted for 5.81%, 1.88% and 1.40% of the total mass of PM2.5 and 11.10%, 2.68%, and 2.48% of the total mass of PM1, respectively. The source identification was conducted for the ionic species in PM2.5 and PM1 aerosols. The results are discussed by the way of correlations and principal component analysis. Spearman correlation indicated that Cl? and K+ in PM2.5 and PM1 can be originated from similar type of sources. Principal component analysis reveals that there are two major sources (anthropogenic and natural such as soil derived particles) for PM2.5 and PM1 fractions.  相似文献   
114.
Summary A new entrainment/detrainment formulation in the Tiedtke’s mass flux cumulus parameterization is discussed here. Apart from validating it with observations both in one and three dimensional cases, it is also evaluated in the light of the results from the original Tiedtke scheme and another mass flux scheme due to Emanuel. The proposed analytical profiles of entrainment and detrainment, easier to implement in any mass flux scheme, give reasonable results in GCM experiments.  相似文献   
115.
We performed modified iterative sandwich experiments (MISE) to determine the composition of carbonatitic melt generated near the solidus of natural, fertile peridotite + CO2 at 1,200–1,245°C and 6.6 GPa. Six iterations were performed with natural peridotite (MixKLB-1: Mg# = 89.7) and ∼10 wt% added carbonate to achieve the equilibrium carbonatite composition. Compositions of melts and coexisting minerals converged to a constant composition after the fourth iteration, with the silicate mineral compositions matching those expected at the solidus of carbonated peridotite at 6.6 GPa and 1,230°C, as determined from a sub-solidus experiment with MixKLB-1 peridotite. Partial melts expected from a carbonated lherzolite at a melt fraction of 0.01–0.05% at 6.6 GPa have the composition of sodic iron-bearing dolomitic carbonatite, with molar Ca/(Ca + Mg) of 0.413 ± 0.001, Ca# [100 × molar Ca/(Ca + Mg + Fe*)] of 37.1 ± 0.1, and Mg# of 83.7 ± 0.6. SiO2, TiO2 and Al2O3 concentrations are 4.1 ± 0.1, 1.0 ± 0.1, and 0.30 ± 0.02 wt%, whereas the Na2O concentration is 4.0 ± 0.2 wt%. Comparison of our results with other iterative sandwich experiments at lower pressures indicate that near-solidus carbonatite derived from mantle lherzolite become less calcic with increasing pressure. Thus carbonatitic melt percolating through the deep mantle must dissolve cpx from surrounding peridotite and precipitate opx. Significant FeO* and Na2O concentrations in near solidus carbonatitic partial melt likely account for the ∼150°C lower solidus temperature of natural carbonated peridotite compared to the solidus of synthetic peridotite in the system CMAS + CO2. The experiments demonstrate that the MISE method can determine the composition of partial melts at very low melt fraction after a small number of iterations.  相似文献   
116.
In this paper, considering the plain strain conditions, a numerical study has been conducted to investigate the behavior of multi layer geosynthetic-reinforced granular bed overlying a soft soil using the Fast Lagrangian Analysis of Continua (FLAC) program. The granular fill, soft soil, and geosynthetic reinforcements are considered as linear elastic materials. The geosynthetic reinforcements are modeled as cable elements fully bonded with the surrounding soil, thus neglecting any slip. The results obtained from the present investigation showed very close agreement when compared with the results of finite element analysis and lumped parameter modeling. The distribution of vertical, lateral and shear stresses in the soil are greatly affected as the number of reinforcement layers is increased. If the tensile stiffness of geosynthetic layers increases and its value is no more than 4,000–5,000 kN/m, the settlement of the reinforced foundation decreases significantly. The reduction in settlement is insignificant when the tensile strength of the geosynthetics exceed the above value.  相似文献   
117.
A nonlinear shallow water model in cylindrical polar coordinate system is developed, using an explicit finite difference scheme with a very fine resolution, to compute different aspects of tsunami at North Sumatra and the adjacent island Simeulue in Indonesia, and the Penang Island in Peninsular Malaysia. The pole of the frame is placed on the mainland of Penang (100.5°E) and the model area extends up to the west of Sumatra (87.5°E). The model is applied to simulate the propagation of tsunami wave towards North Sumatra, Simeulue and Penang Islands associated with Indonesian tsunami of 26 December 2004. The model is also applied to compute water levels along the coastal belts of those islands. Computed and observed water level data are found to be in good agreement and North Sumatra is found to be vulnerable for very high surges. The computed and observed arrival times of high surges are also in reasonable agreement everywhere. Further studies are carried out to investigate the effect of convective terms and it is found that their effects are insignificant in tsunami propagation and weakly significant for wave amplitude very near to the coast.  相似文献   
118.
The paper presents a model for the analysis of granular foundation beds reinforced with several geosynthetic layers. Such reinforced granular beds are often placed on soft soil strata for an efficient and economical transfer of superstructure load. The granular bed is modeled by the Pasternak shear layer and the geosynthetic reinforcement layers by stretched rough elastic membranes. The soft soil is represented by a series of nonlinear springs. The reinforcement has been considered to be extensible and it is assumed that the deformation at the interface of the reinforcements and soil are same. The nonlinear behavior of the granular bed and the soft soil is considered. Plane strain conditions are considered for the loading and reinforced foundation soil system. An iterative finite difference scheme is applied for obtaining the solution and results are presented in nondimensional form. The results from the proposed model are compared to the results obtained for multilayer inextensible geosynthetic reinforcement system. Significant reduction in the settlement has been observed when the number of reinforcement layer is increased. In case of inextensible reinforcements as the number of reinforcement layer is increased the settlement is decreased with a decreasing rate, but in case of extensible reinforcement the reduction rate is almost constant. Nonlinear behavior of the soft soil decreases as number of reinforcement layer is increased. The effect of the stiffness of the geosynthetic layer on the settlement response becomes insignificant for multilayer reinforced system, but the mobilized tension in the reinforcement layers increases as the stiffness of the geosynthetic layers increases.  相似文献   
119.
In this note a comment is made on the total energy content of a blast wave in a stellar model with continuous density distribution. The remark is based on the extensive numerical works carried out by Carruset al. (1951).  相似文献   
120.
To explore the effect of bulk composition on the solidus of carbonated eclogite, we determined near-solidus phase relations at 3 GPa for four different nominally anhydrous, carbonated eclogites. Starting materials (SLEC1, SLEC2, SLEC3, and SLEC4) were prepared by adding variable proportions and compositions of carbonate to a natural eclogite xenolith (66039B) from Salt Lake crater, Hawaii. Near-solidus partial melts for all bulk compositions are Fe–Na calcio-dolomitic and coexist with garnet + clinopyroxene + ilmenite ± calcio-dolomitic solid solution. The solidus for SLEC1 (Ca#=100 × molar Ca/(Ca + Mg + FeT)=32, 1.63 wt% Na2O, and 5 wt% CO2) is bracketed between 1,050°C and 1,075°C (Dasgupta et al. in Earth Planet Sci Lett 227:73–85, 2004), whereas initial melting for SLEC3 (Ca# 41, 1.4 wt% Na2O, and 4.4 wt% CO2) is between 1,175°C and 1,200°C. The solidus for SLEC2 (Ca# 33, 1.75 wt% Na2O, and 15 wt% CO2) is estimated to be near 1,100°C and the solidus for SLEC3 (Ca# 37, 1.47 wt% Na2O, and 2.2 wt% CO2) is between 1,100°C and 1,125°C. Solidus temperatures increase with increasing Ca# of the bulk, owing to the strong influence of the calcite–magnesite binary solidus-minimum on the solidus of carbonate bearing eclogite. Bulk compositions that produce near-solidus crystalline carbonate closer in composition to the minimum along the CaCO3-MgCO3 join have lower solidus temperatures. Variations in total CO2 have significant effect on the solidus if CO2 is added as CaCO3, but not if CO2 is added as a complex mixture that maintains the cationic ratios of the bulk-rock. Thus, as partial melting experiments necessarily have more CO2 than that likely to be found in natural carbonated eclogites, care must be taken to assure that the compositional shifts associated with excess CO2 do not unduly influence melting behavior. Near-solidus dolomite and calcite solid solutions have higher Ca/(Ca + Mg) than bulk eclogite compositions, owing to Ca–Mg exchange equilibrium between carbonates and silicates. Carbonates in natural mantle eclogite, which have low bulk CO2 concentration, will have Ca/Mg buffered by reactions with silicates. Consequently, experiments with high bulk CO2 may not mimic natural carbonated eclogite phase equilibria unless care is taken to ensure that CO2 enrichment does not result in inappropriate equilibrium carbonate compositions. Compositions of eclogite-derived carbonate melt span the range of natural carbonatites from oceanic and continental settings. Ca#s of carbonatitic partial melts of eclogite vary significantly and overlap those of partial melts of carbonated lherzolite, however, for a constant Ca-content, Mg# of carbonatites derived from eclogitic sources are likely to be lower than the Mg# of those generated from peridotite.  相似文献   
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