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Contamination of surface waters by mining wastes in the Milluni Valley (Cordillera Real,Bolivia): Mineralogical and hydrological influences
Authors:Matías Miguel Salvarredy-Aranguren  Anne Probst  Marc Roulet  Marie-Pierre Isaure
Institution:1. Laboratoire des Mécanismes et Transferts en Géologie (LMTG), UMR 5563, CNRS/IRD/UPS, 14 Avenue Edouard Belin, 31400 Toulouse, France;2. ECOLAB UMR 5245, CNRS-INPT-Université Paul Sabatier, ENSAT Avenue de l’Agrobiopole, BP 32607 Auzeville-Tolosane, 31326 Castanet-Tolosan, Cedex, France;3. Institut de Recherche pour le Développement, HYBAM, UMR 154-LMTG, CP 9214 La Paz, Bolivia;4. Equipe Géochimie de l’Environnement, Laboratoire de Géophysique Interne et Tectonophysique (LGIT), UMR 5559 Université J. Fourier and CNRS, BP 53, 38041 Grenoble Cedex 9, France
Abstract:This study is one of very few dealing with mining waste contamination in high altitude, tropical-latitude areas exploited during the last century. Geochemical, mineralogical and hydrological characterizations of potentially harmful elements (PHEs) in surface waters and sediments were performed in the Milluni Valley (main reservoir of water supply of La Paz, Bolivia, 4000 m a.s.l.), throughout different seasons during 2002–2004 to identify contamination sources and sinks, and contamination control parameters. PHE concentrations greatly exceeded the World Health Organization water guidelines for human consumption. The very acidic conditions, which resulted from the oxidation of sulfide minerals in mining waste, favoured the enrichment of dissolved PHEs (Cd > Zn ? As ? Cu ∼ Ni > Pb > Sn) in surface waters downstream from the mine. Stream and lake sediments, mining waste and bedrock showed the highest PHE content in the mining area. With the exception of Fe, the PHEs were derived from specific minerals (Fe, pyrite; Zn, Cd, sphalerite, As, Fe, arsenopyrite, Cu, Fe, chalcopyrite, Pb, galena, Sn, cassiterite), but the mining was responsible for PHEs availability. Most of the PHEs were extremely mobile (As > Fe > Pb > Cd > Zn ∼ Cu > Sn) in the mining wastes and the sediments downstream from the mine. pH and oxyhydroxides mainly explained the contrasted availability of Zn (mostly in labile fractions) and As (associated with Fe-oxyhydroxides). Unexpectedly, Pb, Zn, As, and Fe were significantly attenuated by organic matter in acidic lake sediments.
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