4.6 Article

Natural Cr(VI) contamination of groundwater in the Cecina coastal area and its inner sectors (Tuscany, Italy)

Journal

ENVIRONMENTAL EARTH SCIENCES
Volume 71, Issue 9, Pages 3907-3919

Publisher

SPRINGER
DOI: 10.1007/s12665-013-2776-2

Keywords

Water geochemistry; Natural hexavalent chromium; Water-rock interaction; EQ3/6 software package; Reaction path modelling; Fertilizers; Cecina coastal plain

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A detailed hydrogeochemical study of groundwater in the Cecina coastal plain (Livorno province, Italy) and its inner sectors was undertaken in 2008, as chemical analyses carried out on groundwater since 2006 have revealed Cr(VI) concentrations of up to 49 mu g/L (well above the permissible limit of 5 mu g/L). Ophiolite outcrops are present throughout the study area, and their fragments likely represent a significant portion of the existing multilayered aquifer skeleton. Waters delivered by the serpentinite outcrops have a typically Mg-HCO3 composition, whereas those of the coastal plain are prevailingly of the Ca/Mg-HCO3 type with significant Mg contents. Significant NO3 contamination characterises the studied coastal plain, and an interesting negative correlation exists between Cr(VI) and both NO3 and SO4 deriving from the widespread use of (NH4)(2)SO4 as a farm fertilizer. Chromium speciation calculations carried out using the EQ3NR code reveal that the prevailing Cr(VI) species in solution is CrO4 (2-); however, CaCrO4 degrees and MgCrO4 degrees neutral complexes represent significant percentages (up to 42 %). These findings suggest that the mobility and consequently the bioavailability of Cr(VI) can be significantly enhanced by these neutral complexes, which are not considered to be affected by adsorption/desorption processes. The Cr(VI) source, investigated by means of the Mg/SiO2 molar ratio, seems to be represented mainly by Mg-bearing minerals of the chlorite group. Petrographic observations confirm the occurrence of this mineral group. The interaction between rainwater and the local serpentinite rock was simulated at different and conditions by reaction path modelling using the EQ3/6 software package. was varied in accordance with the assumption that redox conditions are determined in part by NO3. Results are in good agreement with experimental data on spring waters and subordinately with data on some coastal plain groundwater, which plot in a rather wide and field. Although the dissolved Cr content is mostly of natural origin, fertilization may affect its fate.

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