Mercury Accumulation Pathways in a Model Marine Microalgae: Sorption, Uptake, and Partition Kinetics

The accumulation of dissolved mercury (Hg) by phytoplankton is the largest concentration step along aquatic food chains. However, the cell uptake mechanisms remain unclear. In this study, the marine haptophyteTisochrysis lutea, a model phytoplankton species, was examined for its interactions with pi...

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Veröffentlicht in:ACS ES&T water 2024-07, Vol.4 (7), p.2826-2835
Hauptverfasser: Garcia-Arevalo, Isabel, Bérard, Jean-Baptiste, Bieser, Johannes, Le Faucheur, Séverine, Hubert, Clarisse, Lacour, Thomas, Thomas, Bastien, Cossa, Daniel, Knoery, Joël
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Sprache:eng
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Zusammenfassung:The accumulation of dissolved mercury (Hg) by phytoplankton is the largest concentration step along aquatic food chains. However, the cell uptake mechanisms remain unclear. In this study, the marine haptophyteTisochrysis lutea, a model phytoplankton species, was examined for its interactions with picomolar levels of dissolved inorganic divalent Hg (iHg) and monomethyl Hg (MMHg). For both these Hg species, the study observed their successive sorption and internalization over time, yielding Hg partition coefficients as well as sorption, uptake, and release rates. These results were integrated into a time-dependent, three-compartment model for marine cellular Hg accumulation that included exposure medium, phycosphere, and internalized mercury. Assuming equilibria and pseudo-first-order kinetics between compartments, this study obtained transfer rates of Hg between compartments. The results provide insight into the phycosphere as an intermediate compartment for Hg species accumulation and quantify its role in the internalization of Hg. Ultimately, the new model and its parametrization were successfully applied to literature data showing Hg cellular accumulation in different groups of marine phytoplankton, lending confidence in its robustness and potential contributions to help model the uptake of Hg in the aquatic food web.
ISSN:2690-0637
2690-0637
DOI:10.1021/acsestwater.3c00795