Abstract
Heavy metal pollution in sediments derived from the Deûle canal and sampled at different sites not far from a smelting plant has been examined in the present work in order to identify the sources of these metals and to assess the sediment environmental quality. The total concentrations of lead, zinc, cadmium, thallium, indium and tin in the samples were determined using inductively coupled plasma-atomic emission spectroscopy (ICP-AES). Our investigations have revealed that metal pollution is readily apparent in the studied sediments, with metals contents largely exceeding those measured in the background soils: maximum values are obtained for sediments collected near the industrial zone. The chemical forms of Pb, Zn, Cd, Tl, In and Sn in these sediments have also been studied using a sequential extraction method in order to evaluate their possible mobility, bioavailability and toxicity in this aquatic environment. Overall, the averaged fractionation of Pb and Zn is dominated, in a decreasing order, by the easily reducible, oxidizable and carbonate fractions. The importance of oxidizable phase (which is assumed to be composed mainly of organic matter and sulphides) in the Pb and Zn fractionations has been confirmed by the detection of X-ray diffraction peaks ascribed to galena (PbS) and wurtzite (ZnS) in contaminated sediment samples. Anthropogenic Tl, In, and Cd are mainly retained in Fe–Mn oxides/hydroxides, whereas anthropogenic Sn predominates in aluminosilicates/clays. We suspect that elevated percentage levels of Pb, Zn, Cd and In in the reducible fraction constitute a particular potential risk to this aquatic environment in case early diagenetic phenomena (that are observed in the sedimentary material) and physical disturbances (that occur in the water column) both take place strongly in the medium.
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Boughriet, A., Proix, N., Billon, G. et al. Environmental Impacts of Heavy Metal Discharges from a Smelter in Deûle-canal Sediments (Northern France): Concentration Levels and Chemical Fractionation. Water Air Soil Pollut 180, 83–95 (2007). https://doi.org/10.1007/s11270-006-9252-5
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DOI: https://doi.org/10.1007/s11270-006-9252-5