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Paradis, C.J.; Hoss, K.N.; Meurer, C.E.; Hatami, J.L.; Dangelmayr, M.A.; Tigar, A.D.; Johnson, R.H. |
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Title |
Elucidating mobilization mechanisms of uranium during recharge of river water to contaminated groundwater |
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Journal Article |
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Year |
2022 |
Publication |
Journal of Contaminant Hydrology |
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251 |
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104076 |
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Keywords |
Desorption, Dissolution, Groundwater, Surface water, Tracer, Uranium |
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Abstract |
The recharge of stream water below the baseflow water table can mobilize groundwater contaminants, particularly redox-sensitive and sorptive metals such as uranium. However, in-situ tracer experiments that simulate the recharge of stream water to uranium-contaminated groundwater are lacking, thus limiting the understanding of the potential mechanisms that control the mobility of uranium at the field scale. In this study, a field tracer test was conducted by injecting 100 gal (379 l) of oxic river water into a nearby suboxic and uranium-contaminated aquifer. The traced river water was monitored for 18 days in the single injection well and in the twelve surrounding observation wells. Mobilization of uranium from the solid to the aqueous phase was not observed during the tracer test despite its pre-test presence being confirmed on the aquifer sediments from lab-based acid leaching. However, strong evidence of oxidative immobilization of iron and manganese was observed during the tracer test and suggested that immobile uranium was likely in its oxidized state as U(VI) on the aquifer sediments; these observations ruled out oxidation of U(IV) to U(VI) as a potential mobilization mechanism. Therefore, desorption of U(VI) appeared to be the predominant potential mobilization mechanism, yet it was clearly not solely dependent on concentration as evident when considering that uranium-poor river water (\textless0.015 mg/L) was recharged to uranium-rich groundwater (≈1 mg/L). It was possible that uranium desorption was limited by the relatively higher pH and lower alkalinity of the river water as compared to the groundwater; both factors favor immobilization. However, it was likely that the immobile uranium was associated with a mineral phase, as opposed to a sorbed phase, thus desorption may not have been possible. The results of this field tracer study successfully ruled out two common mobilization mechanisms of uranium: (1) oxidative dissolution and (2) concentration-dependent desorption and ruled in the importance of advection, dispersion, and the mineral phase of uranium. |
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0169-7722 |
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THL @ christoph.kuells @ paradis_elucidating_2022 |
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135 |
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N, D.; Panda, B.; S, C.; V, P.M.; Singh, D.K.; L, R.A.; Sahoo, S.K. |
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Title |
Spatio-temporal variations of Uranium in groundwater: Implication to the environment and human health |
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Journal Article |
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Year |
2021 |
Publication |
Science of The Total Environment |
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775 |
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145787 |
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Keywords |
Groundwater, Health risk, Speciation, Stable isotopes, Statistics, Uranium |
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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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0048-9697 |
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THL @ christoph.kuells @ n_spatio-temporal_2021 |
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146 |
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Ola, I.; Drebenstedt, C.; Burgess, R.M.; Mensah, M.; Hoth, N.; Okoroafor, P.; Külls, C. |
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Title |
Assessing petroleum contamination in parts of the Niger Delta based on a sub-catchment delineated field assessment |
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2024 |
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Environmental Monitoring and Assessment |
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196 |
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6 |
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585 |
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The Niger Delta in Nigeria is a complex and heavily contaminated area with over 150,000 interconnected contaminated sites. This intricate issue is compounded by the region’s strong hydrological processes and high-energy environment, necessitating a science-based approach for effective contamination assessment and management. This study introduces the concept of sub-catchment contamination assessment and management, providing an overarching perspective rather than addressing each site individually. A description of the sub-catchment delineation process using the digital elevation model data from an impacted area within the Delta is provided. Additionally, the contamination status from the delineated sub-catchment is reported. Sediment, surface water and groundwater samples from the sub-catchment were analyzed for total petroleum hydrocarbons (TPH) and polycyclic aromatic hydrocarbons (PAHs), respectively. Surface sediment TPH concentrations ranged from 129 to 20,600 mg/kg, with subsurface (2-m depth) concentrations from 15.5 to 729 mg/kg. PAHs in surface and subsurface sediment reached 9.55 mg/kg and 0.46 mg/kg, respectively. Surface water exhibited TPH concentrations from 10 to 620 mg/L, while PAHs ranged from below detection limits to 1 mg/L. Groundwater TPH concentrations spanned 3 to 473 mg/L, with total PAHs varying from below detection limits to 0.28 mg/L. These elevated TPH and PAH levels indicate extensive petroleum contamination in the investigated sediment and water environment. Along with severe impacts on large areas of mangroves and wetlands, comparison of TPH and PAH concentrations with sediment and water quality criteria found 54 to 100% of stations demonstrated exceedances, suggesting adverse biological effects on aquatic and sediment biota are likely occurring. |
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1573-2959 |
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THL @ christoph.kuells @ Ola2024 |
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290 |
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Külls, C. |
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Ecohydrological principles in economic models of water resources in drylands and desert restoration |
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Miscellaneous |
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2014 |
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UNCCD, 2nd Scient. Conf. |
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THL @ christoph.kuells @ Kuells2014ecohydrological |
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68 |
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Külls, C.; Bittner, A. |
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Passive barriers for long-term containment of Uranium and Vanadium |
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Miscellaneous |
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2013 |
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IMWA Conf. |
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THL @ christoph.kuells @ Kuells12013passive |
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69 |
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Külls, C.; Bittner, A.; Marx, V. |
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Strategic Assessment of Water Resources for the Erongo Uranium Province |
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2013 |
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IMWA Conf. |
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THL @ christoph.kuells @ Kuells2012strategic |
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70 |
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Külls, C.; Jobin, J.; Weiler, M. |
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Environmental analytics for water carbon management: enable WCM: Schlussbericht |
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2015 |
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Albert Ludwigs Universität, Professur für Hydrologie |
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THL @ christoph.kuells @ Kuells2015environmental |
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65 |
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Udluft, P.; Dünkeloh, A.; Mederer, J.; Külls, C.; Schaller, J. |
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Re-evaluation of the groundwater resources of Cyprus |
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2006 |
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Lefkosia |
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THL @ christoph.kuells @ Udluft2006re |
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Adar, E.M.; Külls, C. |
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MCM sf–Mixing-cell model for a steady flow MIG–Mixing-cell input generator: A short manual for installation and operation of MCM sf using the MIG–mixing-cell input generator |
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2002 |
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THL @ christoph.kuells @ adar2002mcm |
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Külls, C. |
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Demonstration des Potentials der Nitrat-Isotopenanalytik für die Strategieentwicklung der Sanierung Nitrat-belasteter Brunnen |
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2004 |
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Umweltbundesamt |
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Demonstration des Potentials der Nitrat-Isotopenanalytik für die Strategieentwicklung der Sanierung Nitrat-belasteter Brunnen |
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THL @ christoph.kuells @ |
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