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N, D., Panda, B., S, C., V, P. M., Singh, D. K., L, R. A., et al. (2021). Spatio-temporal variations of Uranium in groundwater: Implication to the environment and human health. Science of The Total Environment, 775, 145787.
Abstract: Groundwater overexploitation has resulted in huge scarcity and increase in the demand for water and food security in India. Groundwater in India has been observed to have experienced various water quality issues like arsenic, fluoride, and Uranium (U) contamination, leading to risk in human health. Markedly, the health risk of higher U in drinking water, as well as its chemical toxicity in groundwater have adverse effects on human. This study has reported occurrence of U as an emerging and widespread phenomenon in South Indian groundwater. Data on U in groundwater were generated from 284 samples along the Cretaceous Tertiary boundary within 4 seasons viz. pre-monsoon (PRM), southwest monsoon (SWM), northeast monsoon (NEM), and post-monsoon (POM). High U concentrations (74 μgL−1) showed to be above the World Health Organization’s provisional guideline value of 30 μgL−1. The geochemical, stable isotope and geophysical studies suggested that U in groundwater could vary with respect to season and was noted to be highest during NEM. The bicarbonate (HCO3) released by weathering process during monsoon could affect the saturation index (SI)Calcite and carbonate species of U. However, the primary source of U was found to be due to geogenic factors, like weathering, dissolution, and groundwater level fluctuation, and that, U mobilization could be enhanced due to anthropogenic activities. The findings further indicated that groundwater in the study area has reached the alarming stage of chemical toxicity. Hence, it is urgent and imperative that workable management strategies for sustainable drinking water source be developed and preventive measures be undertaken, relative to these water quality concerns to mitigate their disconcerting effect on human health.
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Musy, S., & Purtschert, R. (2023). Reviewing 39Ar and 37Ar underground production in shallow depths with implications for groundwater dating. Science of The Total Environment, 884, 163868.
Abstract: Argon-37 (37Ar) and Argon-39 (39Ar) are used for groundwater dating on timescales from weeks to centuries. For both isotopes, the quantification of underground sources is essential to accurately infer water residence times from sampled dissolved activities. Subsurface production resulting from interactions with neutrons from the natural radioactivity in rocks and with primary cosmogenic neutrons has been known for a long time. More recently, the capture of slow negative muons and reactions with muon-induced neutrons were documented for 39Ar subsurface production in the context of underground particle detectors (e.g. for Dark Matter research). However, the contribution from these particles was never considered for groundwater dating applications. Here, we reevaluate the importance of all potential depth-related production channels at depth ranges relevant for 39Ar groundwater dating [0 − 200 meters below the surface (m.b.s)]. The production of radioargon by muon-induced processes is considered in this depth range for the first time. The uncertainty on the total depth-dependent production rate is estimated with Monte Carlo simulations assuming a uniform distribution of the parameter uncertainties. This work aims to provide a comprehensive framework for interpreting 39Ar activities in terms of groundwater residence times and for exposure age dating of rocks. The production of 37Ar is also addressed since this isotope is relevant as a proxy for 39Ar production, for the timing of river-groundwater exchanges, and in the context of on-site inspections (OSI) within the verification framework of the Comprehensive Nuclear-Test-Ban Treaty (CTBT). In this perspective, we provide an interactive web-based application for the calculation of 37Ar and 39Ar production rates in rocks.
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Musy, S., Meyzonnat, G., Barbecot, F., Hunkeler, D., Sültenfuss, J., Solomon, D. K., et al. (2021). In-situ sampling for krypton-85 groundwater dating. Journal of Hydrology X, 11, 100075.
Abstract: Krypton-85 and other radioactive noble gases are widely used for groundwater dating purposes. 85Kr analysis require large volumes of water to reach the analytical requirements. Conventionally, this water is pumped to the surface to be degassed with a gas extraction system. The large pumping rate may disturb the natural flow field and requires substantial field logistics. Hence, we propose a new in-situ degassing method, in which membrane contactors are used to degas the groundwater directly in the well and gas is collected at the surface. This way, field work is facilitated, groundwater system disturbance is minimized, and the gas sample is collected at a specific depth. We demonstrate the tightness of the system regarding atmospheric air contamination for a collection times of 24 h, which is sufficient for both low-level counting and laser-based counting methods for 85Kr. The minimal borehole diameter is 7.5 cm for the prototype presented in this research but can easily be reduced to smaller diameters. In a case study, we compare the results obtained with the new passive method with those from a conventional packer setup sampling. Additionally, 3H/3He samples were collected for both sampling regimes and the dating results were compared with those from 85Kr. A good agreement between tracer ages is demonstrated and the age stratigraphy is consistent with the expected age distribution for a porous unconfined aquifer. In addition, our study emphasizes the differences between the age information sampled with various methods. In conclusion, we demonstrate that the new in situ quasi-passive method provides a more representative age stratigraphy with depth in most cases.
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Müller, M., Alaoui, A., Külls, C., Leistert, H., Meusburger, K., Stumpp, C., et al. (2014). Tracking water pathways in steep hillslopes by δ18O depth profiles of soil water. Journal of hydrology, 519, 340–352.
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Mühr-Ebert, E. L., Wagner, F., & Walther, C. (2019). Speciation of uranium: Compilation of a thermodynamic database and its experimental evaluation using different analytical techniques. Applied Geochemistry, 100, 213–222.
Abstract: Environmental hazards are caused by uranium mining legacies and enhanced radioactivity in utilized groundwater and surface water resources. Knowledge of uranium speciation in these waters is essential for predicting radionuclide migration and for installing effective water purification technology. The validity of the thermodynamic data for the environmental media affected by uranium mining legacies is of utmost importance. Therefore, a comprehensive and consistent database was established according to current knowledge. The uranium data included in the database is based on the NEA TDB (Guillaumont et al., 2003) and is modified or supplemented as necessary e.g. for calcium and magnesium uranyl carbonates. The specific ion interaction theory (Brönsted, 1922) is used to estimate activity constants, which is sufficient for the considered low ionic strengths. The success of this approach was evaluated by comparative experimental investigations and model calculations (PHREEQC (Parkhurst and Appelo, 1999)) for several model systems. The waters differ in pH (2.7–9.8), uranium concentration (10−9-10−4 mol/L) and ionic strength (0.002–0.2 mol/L). We used chemical extraction experiments, ESI-Orbitrap-MS and time-resolved laser-induced fluorescence spectroscopy (TRLFS) to measure the uranium speciation. The latter method is nonintrusive and therefore does not change the chemical composition of the investigated waters. This is very important, because any change of the system under study may also change the speciation.
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