Vogel, J. C., Talma, A. S., & Heaton, T. H. E. (1981). Gaseous nitrogen as evidence for denitrification in groundwater. Journal of Hydrology, 50, 191–200.
Abstract: By investigating the nitrate, oxygen, nitrogen and argon concentrations and 15N14N ratios in artesian groundwater with radiocarbon ages ranging up to 27,000 yr. a process of very slow denitrification in a confined aquifer is demonstrated. The calculated nitrogenisotope fractionation factor associated with this reaction is comparable to that reported for bacterial cultures in vitro and in vivo.
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Zaeri, A., Mohammadi, Z., & Rezanezhad, F. (2023). Determining the source and mechanism of river salinity: An integrated regional study. Journal of Hydrology: Regional Studies, 47, 101411.
Abstract: Study region Zohreh River Basin, Southwest Iran Study focus The salinity of Zohreh River sharply increases in three salinity zones (SZs) along the river named SZ1, SZ2 (the focus of this study), and SZ3. Determining the salinity sources and salinization mechanism using an integrated approach including geological, hydrochemical, isotopic, geophysical, river sinuosity and hydrocarbon analysis are the main objectives of this study. The study focuses on the combination of evidence of regional-scale (i.e., river sinuosity and seismic data) and small-scale (i.e., drilling core analysis). New hydrologic insights for the region Among several known sources of river salinity, it was found that the water quality of the Zohreh River is mainly threatened by the salt-bearing Gachsaran Formation and oil-field brine. It is concluded that halite brine and oil-field brine simultaneously cause the salinization in SZ2, and their contributions were delineated to be 95% and 5%, respectively. The lack of reliable geological evidence to support halite dissolution in surficial layers by circulating waters suggests the possibility of a deep source of halite brine in SZ2. The results revealed that deep halite brine of the salt layers of Gachsaran Formation is mainly responsible for the salinization of SZ2. The mechanism of deep brine penetration to the river through the hidden fault failures detected by the combination of river sinuosity analysis and geophysical data for the first time.
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Dahan, O., Tatarsky, B., Enzel, Y., Külls, C., Seely, M., & Benito, G. (2008). Dynamics of flood water infiltration and ground water recharge in hyperarid desert. Groundwater, 46(3), 450–461.
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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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Uhrie, J. L., Drever, J. I., Colberg, P. J. S., & Nesbitt, C. C. (1996). In situ immobilization of heavy metals associated with uranium leach mines by bacterial sulfate reduction. Hydrometallurgy, 43(1), 231–239.
Abstract: Laboratory experiments with mixed populations of sulfate-reducing bactreria were shown to mediate the removal of milligrams/liter concentrations of uranium, selenium, arsenic and vanadium from aqueous solution via reduction, precipitation and adsorption. Results of laboratory experiments with active sulfidogenic biomass suggest that injection of sulfate and a source of carbon could enhance anaerobic microbial activity in and around uranium leach mines leading to in situ immobilization contaminating metals.
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