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izvor podataka: crosbi

Speciation of mercury in sediments of the Seine estuary (France) (CROSBI ID 85881)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Mikac, Nevenka ; Niessen, Sylvie ; Ouddane, Baghdad ; Wartel, Michel Speciation of mercury in sediments of the Seine estuary (France) // Applied organometallic chemistry, 13 (1999), 10; 715-725-x

Podaci o odgovornosti

Mikac, Nevenka ; Niessen, Sylvie ; Ouddane, Baghdad ; Wartel, Michel

engleski

Speciation of mercury in sediments of the Seine estuary (France)

Although the parameters regulating mercury methylation in sediments are fairly well known, conditions controlling the formation and mobilisation of methylmercury in aquatic sediments are still poorly understood. In this work the environmental factors governing the distribution and behaviour of total and methylmercury within the Seine estuary have been assessed through the analysis of sediment cores. Box-cores taken at a coastal, estuarine and riverine location in the period 1994 to 1997 were analysed for bulk sediment and porewater total and methylmercury concentrations, as well as a number of other chemical variables. Levels of total mercury in sediment (300 - 1000 ngg-1) were found to be uniform all over the estuary and did not show significant temporal or spatial variations. On the contrary, the distribution of methylmercury was distinct from that of its inorganic form since it displayed seasonal and spatial variability. Maximum methylmercury concentrations (up to 6 ngg-1) and percentages (up to 2 %) were obtained at the estuarine location with peak loading just below the sediment surface and a decreasing level in the deeper layers. As total and methylmercury were nor correlated, the temporal and spatial behaviour of methylmercury appeared to reflect variations in salinity, redox potential and the sulphate reduction rate. Low reactive mercury, but very high total mercury levels were measured in the porewaters (10-400 ngl-1) with maximum values at the sediment/water interface. In spite of a high portion of organically complexed dissolved mercury, methylmercury in porewaters was mainly below the detection limit of the method (2 ngl-1). From mercury speciation in the solid phase and dependence of its dissolved fraction on iron and manganese in porewater, the source and distribution of mercury in porewaters are discussed.

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Podaci o izdanju

13 (10)

1999.

715-725-x

objavljeno

0268-2605

Povezanost rada

Kemija

Indeksiranost