Abstract
The lability and controlling factors of arsenic (As) at the sediment-water interface (SWI) are crucial for understanding As behaviors and fates in As-contaminated areas. In this study, we combined high-resolution (5 mm) sampling using diffusive gradients in thin films (DGT) and equilibrium dialysis sampling (HR-Peeper), sequential extraction (BCR), fluorescence signatures, and fluorescence excitation-emission matrices (EEMs)-parallel factor analysis (PARAFAC) to explore the complex mechanisms of As migration in a typical artificially polluted lake, Lake Yangzong (YZ). The study results showed that a high proportion of the reactive As fractions in sediments can resupply pore water in soluble forms during the change from the dry season (winter, oxidizing period) to the rainy season (summer, reductive period). In dry season, the copresence of Fe oxide-As and organic matter (OM)-As complexes was related to the high dissolved As concentration in pore water and limited exchange between the pore water and overlying water. In the rainy season, with the change in redox conditions, the reduction of Fe-Mn oxides and OM degradation by microorganisms resulted in As deposition and exchange with the overlying water. Partial least squares path modelling (PLS-PM) indicated that OM affected the redox and As migration processes through degradation. Based on comprehensive analyses of the As, Fe, Mn, S and OM levels at the SWI, we suggest that the complexation and desorption of dissolved organic matter and Fe oxides play an important role in As cycling. Our findings shed new light on the cascading drivers of As migration and OM features in seasonal lakes and constitute a valuable reference for scenarios with similar conditions.
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