Fate variations of Per- and polyfluoroalkyl substances in diverse aquatic environments: An overlooked influence of hydrodynamics.

Per- and polyfluoroalkyl substances (PFASs) have become a significant global issue; nevertheless, information regarding the hydrodynamic effect on their catchment-scale fate remains lacking. Thus, this study investigated PFASs in water and paired sediment samples from diverse aquatic habitats within the Qinhuai River Basin (QRB), where high concentrations of PFASs are ubiquitous. Rarity score analysis reveals that PFASs were diffusely distributed across the QRB, yet specific sites were identified as emission hotspots. The sediment-water and suspended particulate matter-water partitioning coefficients of PFASs both exhibited significant correlations with chemical structures, ambient variables, land use, and flow velocity (p < 0.05). Flow velocity can promote the liberation of PFASs from particles into water, reducing their accumulation capacity; hence, the higher partitioning coefficients of PFASs were observed in relatively low-velocity aquatic systems, such as lakes, reservoirs, and ponds. A partial least-squares structural equation model was employed to further elucidate their effect pathways and magnitudes on partitioning coefficients. In addition, the primary sources of PFASs were identified, emphasizing their complexity. The ecological risks of PFASs were assessed, indicating priority PFAS species (long-chain PFCAs and HFPO-TA) for management and suggesting water as the preferable environmental medium for regulation. This is the first field investigation to quantify the significance of hydrodynamic influences on the catchment-scale fate of PFASs, improving our understanding of their distribution and behaviors from the perspective of environmental hydraulics.