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Arsenic,iron and organic matter in sediments and groundwater in the Pannonian Basin,Hungary
Institution:1. Eawag: Swiss Federal Institute of Aquatic Science and Technology, Dübendorf, Switzerland;2. Institut International d''Ingénierie de l''Eau et de l''Environnement (2iE), Ouagadougou, Burkina Faso;3. Université Ouaga I Pr. Joseph KI-ZERBO, Ouagadougou, Burkina Faso;4. Centre d''Hydrogéologie et de Géothermie (CHYN), Université de Neuchâtel, Switzerland;1. Department of Environmental Science and Engineering, Faculty of Natural Resources, University of Tehran, Karaj, Iran;2. State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, 18 Shuangqing Road, Haidian District, Beijing 100085, PR China;3. University of Chinese Academy of Sciences, Beijing 100049, PR China
Abstract:In the central part of the Pannonian Basin, factors controlling the distribution of As in sediments and groundwater of the upper 500 m were studied. In core samples, the amounts of As, Fe and Mn extractable with hydroxylamine hydrochloride (NH2OH · HCl) in 25% acetic acid, the proportion of the <0.063 mm size fraction, and the sediment organic C (Corg) contents were measured. In the groundwaters concentrations of As, humic substances, and selected major chemical components were determined. In most core samples extractable Fe, as FeOOH, and Corg are correlated, but some samples have excess Fe, or organic matter. In cases where either excess Fe or excess organic matter is found, the amount of As is also elevated. The spatial distribution of As in the groundwater and the lack of a consistent correlation of As with a single component indicate that there is no single factor controlling the concentration of dissolved As over the entire study area. The only consistent feature is enrichment of As relative to Fe in the groundwater, compared to the sediments. This suggests that the dissolution of Fe minerals, which primarily adsorb As, is not congruent. In reducing conditions Fe(III) oxyhydroxides together with adsorbed As dissolve, and siderite with little or no As precipitates. When sub-regions are separated and studied individually, it can be shown that hydrogeological features of the sediments, the proportions of Fe minerals and sedimentary organic matter, and the concentration of dissolved humic materials, all influence the accumulation and mobilization of As. The significance of the different mobilizing processes, however, and the mean concentration of As, is different in the recharge, through-flow and discharge areas.
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