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Dutova, E. M., Nikitenkov, A. N., Pokrovskiy, V. D., Banks, D., Frengstad, B. S., & Parnachev, V. P. (2017). Modelling of the dissolution and reprecipitation of uranium under oxidising conditions in the zone of shallow groundwater circulation. Journal of Environmental Radioactivity, 178-179, 63–76.
Abstract: Generic hydrochemical modelling of a grantoid-groundwater system, using the Russian software “HydroGeo”, has been carried out with an emphasis on simulating the accumulation of uranium in the aqueous phase. The baseline model run simulates shallow granitoid aquifers (U content 5 ppm) under conditions broadly representative of southern Norway and southwestern Siberia: i.e. temperature 10 °C, equilibrated with a soil gas partial CO2 pressure (PCO2, open system) of 10−2.5 atm. and a mildly oxidising redox environment (Eh = +50 mV). Modelling indicates that aqueous uranium accumulates in parallel with total dissolved solids (or groundwater mineralisation M – regarded as an indicator of degree of hydrochemical evolution), accumulating most rapidly when M = 550–1000 mg L−1. Accumulation slows at the onset of saturation and precipitation of secondary uranium minerals at M = c. 1000 mg L−1 (which, under baseline modelling conditions, also corresponds approximately to calcite saturation and transition to Na-HCO3 hydrofacies). The secondary minerals are typically “black” uranium oxides of mixed oxidation state (e.g. U3O7 and U4O9). For rock U content of 5–50 ppm, it is possible to generate a wide variety of aqueous uranium concentrations, up to a maximum of just over 1 mg L−1, but with typical concentrations of up to 10 μg L−1 for modest degrees of hydrochemical maturity (as indicated by M). These observations correspond extremely well with real groundwater analyses from the Altai-Sayan region of Russia and Norwegian crystalline bedrock aquifers. The timing (with respect to M) and degree of aqueous uranium accumulation are also sensitive to Eh (greater mobilisation at higher Eh), uranium content of rocks (aqueous concentration increases as rock content increases) and PCO2 (low PCO2 favours higher pH, rapid accumulation of aqueous U and earlier saturation with respect to uranium minerals).
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Robati, A., & Barani, G. A. (2009). Modeling of water surface profile in subterranean channel by differential quadrature method (DQM). Applied Mathematical Modelling, 33(3), 1295–1305.
Abstract: This study, investigates the hydraulic of flow in a subterranean channel headspring. The continuity and momentum equations of flow in porous media considering real conditions were used and the basic equation of flow in a subterranean channel was resulted. This equation is very similar to the spatially varied flow with increasing discharge. An equation, defining the hydraulic parameters of a subterranean channel section was adopted. Then differential quadrature method (DQM), was applied to the equation of flow in subterranean channel, consequently the water surface profile was resulted. To illustrate the rightness of model, the hydraulic parameters of flow in the Gavgard branch of the Joopar Goharriz Qanat were measured and the water surface profile was determined. This water surface profile was compared to the water surface profile computed by the model, which are in good agreement.
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Gómez, P., Garralón, A., Buil, B., Turrero, M. J., Sánchez, L., & Cruz, B. de la. (2006). Modeling of geochemical processes related to uranium mobilization in the groundwater of a uranium mine. Science of The Total Environment, 366(1), 295–309.
Abstract: This paper describes the processes leading to uranium distribution in the groundwater of five boreholes near a restored uranium mine (dug in granite), and the environmental impact of restoration work in the discharge area. The groundwater uranium content varied from \textless1 μg/L in reduced water far from the area of influence of the uranium ore-containing dyke, to 104 μg/L in a borehole hydraulically connected to the mine. These values, however, fail to reflect a chemical equilibrium between the water and the pure mineral phases. A model for the mobilization of uranium in this groundwater is therefore proposed. This involves the percolation of oxidized waters through the fractured granite, leading to the oxidation of pyrite and arsenopyrite and the precipitation of iron oxyhydroxides. This in turn leads to the dissolution of the primary pitchblende and, subsequently, the release of U(VI) species to the groundwater. These U(VI) species are retained by iron hydroxides. Secondary uranium species are eventually formed as reducing conditions are re-established due to water–rock interactions.
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Kirchner, J. W. (2023). Mixing Models With Multiple, Overlapping, or Incomplete End-Members, Quantified Using Time Series of a Single Tracer. Geophysical Research Letters, 50(12), 2023.
Abstract: Abstract Mixing models are used throughout earth and environmental science to quantify the relative contributions of sources to mixtures, based on chemical or isotopic tracers. Often, however, some end-members are missing or their tracer distributions overlap, precluding the use of conventional mixing models. Here I show how these constraints can be overcome by exploiting the information contained in tracer time-series fluctuations. This approach, ensemble end-member mixing analysis (EEMMA), can potentially quantify many sources using a single tracer, even if their mean concentrations are indistinguishable. EEMMA can also quantify source contributions when some sources are unknown, and even infer the tracer time series of a missing source. Benchmark tests with synthetic data verify the reliability of this approach, thus expanding the range of mixing models that can be quantified using tracer time series. An R script is provided for the necessary calculations, including error propagation.
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Khoury, H. N., salameh, E. M., & Clark, I. D. (2014). Mineralogy and origin of surficial uranium deposits hosted in travertine and calcrete from central Jordan. Applied Geochemistry, 43, 49–65.
Abstract: Secondary uranium encrustations are hosted in thick travertine and calcrete deposits of Pleistocene–Recent age in central Jordan. The central Jordan varicolored marble and travertine are equivalent to the active metamorphic area in Maqarin, north Jordan. More than 100 samples were collected from the outcrops of the varicolored marble, travertine, calcrete, and the yellow uranium encrustations. The secondary yellow encrustations are mainly composed of uranyl vanadate complexes. Tyuyamunite Ca(UO2)2V25+O8·3(H2O)–strelkinite Na2(UO2)2V2O8·6(H2O) solid solution series are the major components and their composition reflects changes in the Ca/Na ratio in solution. Potentially, new vanadium free calcium uranate phases (restricted to the varicolored marble) were identified with CaO:UO3 ratios different from the known mineral vorlanite (CaU6+)O4. Carbon and oxygen isotope data from calcite in the varicolored marble are characterized by Rayleigh-type enrichment in light isotopes associated with release of 13C and 18O enriched CO2 by high temperature decarbonation during combustion of the bituminous marl. Stable isotope results from uranium hosted travertine and calcrete varieties exhibit a wide range in isotopic values, between decarbonated and normal sedimentary carbonate rocks. The depleted δ13C and δ18O values in the travertine are related to the kinetic reaction of atmospheric CO2 with hyperalkaline Ca(OH)2 water. The gradual enrichment of δ13C and δ18O values in the calcrete towards equilibrium with the surrounding environment is related to continuous evaporation during seasonal dry periods. Uranium mineralization in central Jordan resulted from the interplay of tectonic, climatic, hydrologic, and depositional events. The large distribution of surficial uranium occurrences hosted in travertine and calcrete deposits is related to the artesian ascending groundwater that formed extensive lakes along NNW–SSE trending depressions. Fresh groundwater moved upward through the highly fractured phosphate, bituminous marl and varicolored marble to form unusual highly alkaline water (hydroxide–sulfate type) enriched with sensitive redox elements among which were U and V.
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Ren, Y., Yang, X., Hu, X., Wei, J., & Tang, C. (2022). Mineralogical and geochemical evidence for biogenic uranium mineralization in northern Songliao Basin, NE China. Ore Geology Reviews, 141, 104556.
Abstract: The sandstone-hosted uranium mineralization areas in the Sanzhao Sag of the northern Songliao Basin have been newly identified. The target stratum is the Upper Cretaceous Sifangtai Formation and the uranium mineralization mainly occurs in the bottom of Sifangtai Formation, corresponding to channel sand bodies in meandering river system, characterized by medium to fine-grained sandstone. This study proposes the uranium metallogenic model through petrographic observation, whole rock geochemistry, mineralogical study of uranium occurrence form (SEM), organic matter rock–eval pyrolysis analysis (REP) and in-situ sulfur isotope determination of different generations of pyrite by LA-MC-ICP-MS. Compared with the sandstones collected in barren reduction and oxidization zones, the mineralized sandstones show obvious increase in the contents of TOC, total sulfur, Y and U. Petrographic observations indicate that organic matters are mainly inherited from land plants. REP data display that the organic matter (OM) disseminated in the sandstone has very low hydrogen index (HI) from around 0 to 21 mg HC/g TOC and varied oxygen index (OI) from 44 to 115 mg CO2/g TOC, corresponding to Type Ⅳ kerogen (degraded kerogen). There are two types of coffinite with different grain size, micro-particles (μm-sized) and large aggregates (generally up to 100 μm) respectively. The coffinite micro spherules exhibit short rod-like or worm-like morphology occurring in clay matrix and cell cavities in degradofusinite or around subidiomorphic-idiomorphic pyrite. The coarse-grained coffinite contains other mineral facies (e.g. pyrite, quartz) and some of large coffinite aggregates display thrombolite-type microbial structures. The irregular pyrite relict particles in coarse-grained colloidal coffinite have light sulfur isotope compositions characterized by δ34S values from –39.96‰ to –49.89‰. The δ34S values of colloidal pyrite in replacement of OM or of the sub-idiomorphic FeS2 cement filling in the cavities of OM range from –52.77‰ to –13.88‰. Some of sub-idiomorphic pyrite cement and idiomorphic crystal have the heavier signature from – 27.06‰ to + 14.23‰. The light sulfur isotope signature suggests that the sulfur originates from bacterial sulfate reduction (BSR). The OM replacement by pyrite and the highest OI values recorded by REP in uranium mineralized samples are lines of evidence of biodegradation. Bacteria use the organic matter as food source and produce isotopically light reduced sulfur species. Oxygenated uranium-bearing waters infiltrated through the denudated windows at Daqing placanticline into the porous reduced sandstones deposited in the Sanzhao Sag. Uranium was indirectly reduced by BSR-derived iron disulfides or directly reduced by sulfate-reducing bacteria.
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Min, M., Chen, J., Wang, J., Wei, G., & Fayek, M. (2005). Mineral paragenesis and textures associated with sandstone-hosted roll-front uranium deposits, NW China. Ore Geology Reviews, 26(1), 51–69.
Abstract: We present a first paragenetic study of the Wuyier, Wuyisan, Wuyiyi and Shihongtan sandstone-hosted roll-front uranium deposits, northwest China. The mineralization is hosted by Lower–Middle Jurassic coarse- to medium-grained sandstones, which are dark-gray to black due to a mixture of ore minerals and carbonaceous debris. The sandstone is alluvial fan-braided river facies. Minerals associated with these deposits can be broadly categorized as detrital, authigenic, and ore-stage mineralization. Ore minerals consist of uraninite and coffinite. This is the first noted occurrence of coffinite in this type of deposit in China. Sulfide minerals associated with the uranium minerals are pyrite, marcasite, and less commonly, sphalerite and galena. The sulfide minerals are largely in textural equilibrium with the uranium minerals. However, these sulfide minerals occasionally appear to predate, as well as postdate, the uranium minerals. This implies that there are multiple generations of sulfides associated with these deposits. The ore minerals occur interstitially between fossilized wood cells in the sandstones as well as replace fossilized wood and biotite. The deposits are generally low-grade. Primary uranium minerals associated with the low-grade deposits are generally too small, ranging from 0.2 to 0.3 μm in diameter, to be observed by optical microscopy and are only observed by electron microscopy. Mineral paragenesis and textures indicate that these deposits formed under low temperature (30–50 °C) conditions.
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Sahoo, P. K., Virk, H. S., Powell, M. A., Kumar, R., Pattanaik, J. K., Salomão, G. N., et al. (2022). Meta-analysis of uranium contamination in groundwater of the alluvial plains of Punjab, northwest India: Status, health risk, and hydrogeochemical processes. Science of The Total Environment, 807, 151753.
Abstract: Despite numerous studies, there are many knowledge gaps in our understanding of uranium (U) contamination in the alluvial aquifers of Punjab, India. In this study, a large hydrogeochemical dataset was compiled to better understand the major factors controlling the mobility and enrichment of uranium (U) in this groundwater system. The results showed that shallow groundwaters (\textless60 m) are more contaminated with U than from deeper depths (\textgreater60 m). This effect was predominant in the Southwest districts of the Malwa, facing significant risk due to chemical toxicity of U. Groundwaters are mostly oxidizing and alkaline (median pH: 7.25 to 7.33) in nature. Spearman correlation analysis showed that U concentrations are more closely related to total dissolved solids (TDS), salinity, Na, K, HCO3−, NO3− Cl−, and F− in shallow water than deep water, but TDS and salinity remained highly correlated (U-TDS: ρ = 0.5 to 0.6; U-salinity: ρ = 0.5). This correlation suggests that the salt effect due to high competition between ions is the principal cause of U mobilization. This effect is evident when the U level increased with increasing mixed water species (Na-Cl, Mg-Cl, and Na-HCO3). Speciation data showed that the most dominant U species are Ca2UO2(CO3)2− and CaUO2(CO3)3−, which are responsible for the U mobility. Based on the field parameters, TDS along with pH and oxidation-reduction potential (ORP) were better fitted to U concentration above the WHO guideline value (30 μg.L−1), thus this combination could be used as a quick indicator of U contamination. The strong positive correlation of U with F− (ρ = 0.5) in shallow waters indicates that their primary source is geogenic, while anthropogenic factors such as canal irrigation, groundwater table decline, and use of agrochemicals (mainly nitrate fertilizers) as well as climate-related factors i.e., high evaporation under arid/semi-arid climatic conditions, which result in higher redox and TDS/salinity levels, may greatly affect enrichment of U. The geochemical rationale of this study will provide Science-based-policy implications for U health risk assessment in this region and further extrapolate these findings to other arid/semi-arid areas worldwide.
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Bresinsky, L., Kordilla, J., Hector, T., Engelhardt, I., Livshitz, Y., & Sauter, M. (2023). Managing climate change impacts on the Western Mountain Aquifer: Implications for Mediterranean karst groundwater resources. Journal of Hydrology X, 20, 100153.
Abstract: Many studies highlight the decrease in precipitation due to climate change in the Mediterranean region, making it a prominent hotspot. This study examines the combined impacts of climate change and three groundwater demand scenarios on the water resources of the Western Mountain Aquifer (WMA) in Israel and the West Bank. While commonly used methods for quantifying groundwater recharge and water resources rely on regression models, it is important to acknowledge their limitations when assessing climate change impacts. Regression models and other data-driven approaches are effective within observed variability but may lack predictive power when extrapolated to conditions beyond historical fluctuations. A comprehensive assessment requires distributed process-based numerical models incorporating a broader range of relevant physical flow processes and, ideally, ensemble model projections. In this study, we simulate the dynamics of dual-domain infiltration and precipitation partitioning using a HydroGeoSphere (HGS) model for variably saturated water flow coupled to a soil-epikarst water balance model in the WMA. The model input includes downscaled high-resolution climate projections until 2070 based on the IPCC RCP4.5 scenario. The results reveal a 5% to 10% decrease in long-term average groundwater recharge compared to a 30% reduction in average precipitation. The heterogeneity of karstic flow and increased intensity of individual rainfall events contribute to this mitigated impact on groundwater recharge, underscoring the importance of spatiotemporally resolved climate models with daily precipitation data. However, despite the moderate decrease in recharge, the study highlights the increasing length and severity of consecutive drought years with low recharge values. It emphasizes the need to adjust current management practices to climate change, as freshwater demand is expected to rise during these periods. Additionally, the study examines the emergence of hydrogeological droughts and their propagation from the surface to the groundwater. The results suggest that the 48-month standardized precipitation index (SPI-48) is a suitable indicator for hydrogeological drought emergence due to reduced groundwater recharge.
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Karaimeh, S. A. (2019). Maintaining desert cultivation: Roman, Byzantine, and Early Islamic water-strategies at Udhruh region, Jordan. Journal of Arid Environments, 166, 108–115.
Abstract: The site of Udhruh is located in the arid desert of southern Jordan, about 15 km to the east of Petra. The site was built by the Nabataeans but expanded by the Romans (as a defensive site) and was continuously occupied until the Early Islamic period. It receives less than the 200 mm of annual precipitation, which is crucial for agricultural cultivation. Archaeological evidence from earlier excavations together with new data from several survey projects indicate that areas around Udhruh were cultivated throughout the Roman, Byzantine, and Early Islamic periods (300 BCE–800 CE). The fundamental question is: how did the people of Udhruh sustain their community in the desert, and how did they transform the desert into arable land? The landscape could be utilised thanks to sophisticated water management and irrigation techniques. At least four underground qanat systems were identified providing Udhruh with access to groundwater. At the terminal end of the qanat systems, several types of closed surface channels conveyed the water to reservoirs, which subsequently distributed the water to the field systems. The water systems of Udhruh differ from the well-known Nabataean systems in the surrounding area. As Udhruh was taken over by the Roman army in 106 CE, this study analyses how the Nabataean water systems continued to function and adapt through the Roman and Byzantine periods. A complete understanding of Udhruh’s water systems helps to reconstruct past land use, agricultural activity, and irrigation practices in a currently arid region.
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