Abstract
Benzotriazoles (BTRs), benzothiazoles (BTHs), and benzotriazole UV stabilizers (BUVs) have attracted increasing attention due to their ubiquity in the environment, toxicity, and potential ecological risks. However, information on their distributions in the ocean is scarce. In this study, BTRs, BTHs, and BUVs were firstly determined in the surface seawater, sea-surface microlayer (SML), suspended particulate matter (SPM), and sediments of the Yellow Sea (YS) and East China Sea (ECS). The spatial distributions of BTRs, BTHs, and BUVs in the YS and ECS showed offshore decreasing trend in their concentrations, indicating that terrestrial inputs from runoff and rivers had important influences on their distributions. The organic carbon normalized partition coefficients (log Koc) of target contaminants in surface seawater-SPM (3.06–4.16 L/g) and bottom seawater-sediment (2.55–4.82 L/kg) systems were determined. SPM showed greater sorption capacities for most target contaminants than the sediment. The burial capacities of BTHs, BTRs, and BUVs from SPM to surface sediments were evaluated using their respective log Kow values and their sedimentary fluxes in the YS and ECS were quantified. BTRs, BTHs, and BUVs were enriched in the SML, with the enrichment extents of the suspended particulate phase being obviously lower than those of the dissolved phase. The ecological risks of BTRs, BTHs, and BUVs were evaluated using the risk quotient (RQ) method, which showed no toxic risk to aquatic organisms throughout the water phases, but high risk in nearshore sediments.
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