Retrofit-reinforcement of cohesive soil slopes using high strength geotextiles with drainage capability

A series of geotechnical centrifuge physical modeling tests were performed to assess the potential use of a new cost-effective mechanically stabilized earth system for retrofitting marginally stable cohesive slopes. The proposed system utilizes the dual functions of reinforcement and drainage by directly inserting high strength non-woven geotextile strips into slopes, with little or no excavation required behind the slope face. The system significantly increases the factor of safety of potentially unstable cohesive slopes, and can be constructed at less expense and more rapidly than conventional mechanically stabilized earth systems.     

Karst database development in Minnesota: design and data assembly

The Karst Feature Database (KFD) of Minnesota is a relational GIS-based Database Management System (DBMS). Previous karst feature datasets used inconsistent attributes to describe karst features in different areas of Minnesota. Existing metadata were modified and standardized to represent a comprehensive metadata for all the karst features in Minnesota. Microsoft Access 2000 and ArcView 3.2 were used to develop this working database. Existing county and sub-county karst feature datasets have been assembled into the KFD, which is capable of visualizing and analyzing the entire data set. By November 17 2002, 11,682 karst features were stored in the KFD of Minnesota. Data tables are stored in a Microsoft Access 2000 DBMS and linked to corresponding ArcView applications. The current KFD of Minnesota has been moved from a Windows NT server to a Windows 2000 Citrix server accessible to researchers and planners through networked interfaces.     

A preliminary investigation into the use of ochre as a remedial amendment in arsenic-contaminated soils

Ochre is an unwanted waste product that accumulates in wetlands and streams draining abandoned coal and metal mines. A potential commercial use for ochre is to remediate As contaminated soil. Arsenic contaminated soil (605 mg kg⁻¹) was mixed with different ochres (A, B and C) in a mass ratio of 1:1 and shaken in 20 mL of deionised water. After 72 h As concentration in solution was ca. 500 μg kg⁻¹ in the control and 1–2.5 μg kg⁻¹ in the ochre treated experiments. In a second experiment soil:ochre mixtures of 0.05–1:1 were shaken in 20 mL of deionised water for 24 h. For Ochres A and C, as solution concentration was reduced to ca. 1 μg kg⁻¹ by 0.2–1:1 ochre:soil mixtures. For Ochre B, as concentration only reached ca. 1 μg kg⁻¹ in the 1:1 ochre:soil mix. Sorption of As was best modelled by a Freundlich isotherm using As sorption per mass of goethite in the ochre (log K = 1.64, n = 0.79, R² = 0.76, p 0.001). Efficiency of ochre in removing As from solution increased with increasing total Fe, goethite, citrate dithionite extractable Fe and surface area.     

Petrology of the Jurassic Shah-Kuh granite (eastern Iran), with reference to tin mineralization

The Shah-Kuh granitic pluton of eastern Central Iran was emplaced 165 Ma ago, in an active continental margin setting. It is made of two main units: a granodioritic unit (SiO₂=63–71 wt%) to the north–west and a syenogranitic unit (SiO₂=73–77 wt%) to the south–east. The former unit displays seriate medium-grained textures and contains locally abundant mafic enclaves. The latter unit is medium- to coarse-grained and porphyritic, with 0.5–3 cm long K-feldspar megacrysts. Fine-grained granitic bodies are present in both units. The rocks are metaluminous to slightly peraluminous (I-type) and peraluminous (S-type) and belong to the ilmenite-series granites. Fractional crystallization appears to have been a very effective differentiation process in both units, and the fractionated mineral assemblages are determined by mass balance calculations. Isotopic data (Sr_i=0.7065 and εNdt=−2.5) are consistent with a young upper crustal protolith. Tin mineralization in sheeted quartz-tourmaline (-cassiterite) veins is spatially associated with the granodioritic unit. The veins formed by hydraulic fracturing when the granodioritic to monzogranitic magma became water-saturated and exsolved a fluid phase during crystallization. The reduced nature of this magma is responsible for the incompatible behaviour of Sn, likely to favour Sn concentration in the residual melt and then in the exsolved fluid. Another fluid phase was exsolved by the syenogranitic magma and was responsible for local greisenized granites, characterized by high Y and HREE-contents and non-fractionated REE distribution patterns. Field and mineralogical data show that the (B, Sn) vein-forming fluid was different from the (F, Li) greisen-forming fluid.     

Intraplate deformation and 3D rheological structure of the Rhine Rift System and adjacent areas of the northern Alpine foreland

The lithosphere of the Northern Alpine foreland has undergone a polyphase evolution during which interacting stress-induced intraplate deformation and upper mantle thermal perturbations controlled folding of the thermally weakened lithosphere. In this paper we address relationships among deeper lithospheric processes, neotectonics and surface processes in the Northern Alpine foreland with special emphasis on tectonically induced topography. We focus on lithosphere memory and neotectonics, paying special attention to the thermo-mechanical structure of the Rhine Graben System and adjacent areas of the northern Alpine foreland lithosphere. We discuss implications for mechanisms of large-scale intraplate deformation and links with surface processes and topography evolution.     

Development of an integrated conceptual model for the rational management of the transboundary Nestos River, Greece

This paper provides a detailed analysis of the geologic, hydrologic and hydrogeologic characteristics of Nestos River basin, which is formed within the Greek mountainous part of the river. The quantitative analysis was mainly based on the data of the river flow in different gauging points across the rivercourse as well as on the data of groundwater discharge from karst springs of the mountainous area while important conclusions were made regarding the hydraulic connection between the surface waters of the river and the groundwater of the karst aquifers of the basin. The qualitative analysis has shown that the quality of both surface waters and groundwaters of the investigated basin is high, whereas, no sources of contamination were indicated during this research. The possible effects of the two large dams of Platanovrisi and Thesavros are also analysed as they strongly affect the quantitative and qualitative regime of the river delta.     

Temporal and spatial variations in water flow and sediment load in Narmada River Basin, India: natural and man-made factors

The Narmada River flows through the Deccan volcanics and transports water and sediments to the adjacent Arabian Sea. In a first-ever attempt, spatial and temporal (annual, seasonal, monthly and daily) variations in water discharge and sediment loads of Narmada River and its tributaries and the probable causes for these variations are discussed. The study has been carried out with data from twenty-two years of daily water discharge at nineteen locations and sediment concentrations data at fourteen locations in the entire Narmada River Basin. Water flow in the river is a major factor influencing sediment loads in the river. The monsoon season, which accounts for 85 to 95% of total annual rainfall in the basin, is the main source of water flow in the river. Almost 85 to 98% of annual sediment loads in the river are transported during the monsoon season (June to November). The average annual sediment flux to the Arabian Sea at Garudeshwar (farthest downstream location) is 34.29×10⁶ t year⁻¹ with a water discharge of 23.57 km³ year⁻¹. These numbers are the latest and revised estimates for Narmada River. Water flow in the river is influenced by rainfall, catchment area and groundwater inputs, whereas rainfall intensity, geology/soil characteristics of the catchment area and presence of reservoirs/dams play a major role in sediment discharge. The largest dam in the basin, namely Sardar Sarovar Dam, traps almost 60–80% of sediments carried by the river before it reaches the Arabian Sea.     

H2S fluxes from Mt. Etna, Stromboli, and Vulcano (Italy) and implications for the sulfur budget at volcanoes

We present here new measurements of sulfur dioxide and hydrogen sulfide emissions from Vulcano, Etna, and Stromboli (Italy), made by direct sampling at vents and by filter pack and ultraviolet spectroscopy in downwind plumes. Measurements at the F0 and FA fumaroles on Vulcano yielded SO₂/H₂S molar ratios of ≈0.38 and ≈1.4, respectively, from which we estimate an H₂S flux of 6 to 9 t · d⁻¹ for the summit crater. For Mt. Etna and Stromboli, we found SO₂/H₂S molar ratios of ≈20 and ≈15, respectively, which combined with SO₂ flux measurements, suggest H₂S emission rates of 50 to 113 t · d⁻¹ and 4 to 8 t · d⁻¹, respectively. We observe that “source” and plume SO₂/H₂S ratios at Vulcano are similar, suggesting that hydrogen sulfide is essentially inert on timescales of seconds to minutes. This finding has important implications for estimates of volcanic total sulfur budget at volcanoes since most existing measurements do not account for H₂S emission.     

Calculation of the UV-visible spectra and the stability of Mo and Re oxysulfides in aqueous solution

Erickson and Helz (2000) established that molybdate, MoO₄⁻², is quickly and completely transformed to thiomolybdate, MoS₄⁻², by reaction with sulfide. They monitored the equilibria and kinetics of this process by measuring the UV-visible spectra of solutions containing the different oxythiomolybdate species. There is interest in the analogous reactions for the ReO₄⁻ species but little experimental data. We have therefore calculated quantum-chemically the equilibrium constants in solution for the sulfidation reactions of both MoO₄⁻² and ReO₄⁻, as well as recalculating their UV-visible charge-transfer spectra. Calculations using configuration interaction singles and time-dependent hybrid Hartree-Fock density functional methods give good absolute values and trends in UV-vis energies for both series. For MoO₄⁻² the calculated equilibrium constants for the various sulfidation steps match reasonably well against the experimental values (within two log K units). For the ReO₄⁻ sulfidation reaction the first two steps are considerably less favorable than for MoO₄⁻², suggesting that the “geochemical switch” of Erickson and Helz, a rapid transformation of oxyanion to thioanion highly dependent on sulfide concentration, will be less effective in the Re case. However, both our calculations and experiment indicate that ReO₄⁻ and ReS₄⁻ are both easier to reduce than their Mo analogs, so that reduction of these Re(VII) species will be the preferred mechanism for their removal from seawater. A previous suggestion that the neutral species MoO₄H₂ is actually the hydrated octahedral Mo(OH)₆ species is found to be incorrect, but the MoO₃(OH₂)₃ species, a highly distorted six-coordinate complex, is almost competitive in energy with MoO₄H₂ plus two H₂O.