Abstract
Mercury (Hg) methylation was studied in water,sediment and Eichhornia crassipesroots of a freshwater lake, in Rio de Janeiro(Brazil). Samples were incubated with203HgCl2 and the Me203Hg producedwas measured by liquid scintillation.Methylmercury (MeHg) production was <10-3% in water, low in sediment (up to5.8%) and high in E. crassipesroots (21–27%). Higher MeHg formation wasfound in aerobic conditions for the roots and inanaerobic conditions for the sediment.Methylation increased with incubation time, upto 5 days. A 3-day incubation period was used inthe majority of the assays, to avoid large scalephysico-chemical changes inside the incubationflasks. Methylation was not detected inheat-sterilized root samples. Sodium sulphatestimulated Hg methylation while sodium molybdateinhibited the process in samples incubated for3, 6, 12, 24, 48 and 72 hr. This suggeststhat sulphidogenic bacteria are responsible forthe methylation process. Experiments with rootsstored at 5 and 25 °C fordifferent periods before incubation, indicatethat methylation is modified by storage time and temperature.
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Mauro, J.B.N., Guimarães, J.R.D. & Melamed, R. Mercury Methylation in Macrophyte Roots of a Tropical Lake. Water, Air, & Soil Pollution 127, 271–280 (2001). https://doi.org/10.1023/A:1005222902966
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DOI: https://doi.org/10.1023/A:1005222902966