Barber, Andrew; Mirzaei, Yeganeh 
ORCID: https://orcid.org/0000-0003-2317-1841; Brandes, Jay ORCID: https://orcid.org/0000-0001-9911-4734; Joshani, Azadeh; Gobeil, Charles et Gélinas, Yves
(2024).
Redox conditions influence the chemical composition of iron-associated organic carbon in boreal lake sediments: A synchrotron-based NEXAFS study.
Geochimica et Cosmochimica Acta
, vol. 382
.
pp. 51-60.
DOI: 10.1016/j.gca.2024.08.018.
Résumé
The global carbon and iron cycles are intimately linked as redox-sensitive iron oxides readily bind organic carbon in a variety of environmental settings, including marine and lacustrine sediments. While these iron-organic carbon complexes sequester vast quantities of organic carbon, the composition of the organic matter within them remains unknown for lacustrine environments. Here we present C K1s and Fe L3,2 edge Near Edge X-ray Absorption Fine Structure (NEXAFS) spectra of surface sediments and authigenic iron complexes from adjacent basins of a pristine boreal lake located in Québec, Canada, with contrasting oxygen exposure regimes. We demonstrate differences in organic carbon speciation in sediments from both basins, as well as co-localization of organic carbon and iron on a sub-micron scale in 100 nm thick samples. Differences in redox cycling across these two basins allow for a direct comparison of the effect of oscillating redox conditions on the composition of organic carbon sequestered by iron. Our results suggest that reactive organic molecules, which may be polysaccharides, were found preferentially associated with iron in the perennially oxic sediments compared to more phenol rich organics in the seasonally anoxic sediments, highlighting the importance of iron oxides in the protection and preservation of labile organic compounds. Traces of aliphatic carbon were observed in sediments from the anoxic basin, alongside carboxyl and aromatic functionalities. This carboxyl-rich aliphatic material could possibly interact with the sediment mineral matrix either through a ligand exchange mechanism between the mineral phases and the carboxyl functionalities, or via non-specific hydrophobic interactions involving the aliphatic moieties. Finally, our work also shows that OC:Fe ratios should be used with caution when inferring a binding mechanism between OC and iron oxides.
| Type de document: | Article |
|---|---|
| Mots-clés libres: | organic carbon cycling; iron hydroxides; lake sediments; X-ray analysis; synchrotron; NEXAFS analysis |
| Centre: | Centre Eau Terre Environnement |
| Date de dépôt: | 08 nov. 2024 19:41 |
| Dernière modification: | 08 nov. 2024 19:41 |
| URI: | https://espace.inrs.ca/id/eprint/15951 |
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