MAPPING PFAS, MAJOR AND TRACE ELEMENTS, STABLE ISOTOPES, AND RECHARGE-AGES IN 3-DIMENSIONS IN THE FRACTURED ROCK AQUIFER BENEATH THE RUTLAND SOUTHERN VERMONT REGIONAL AIRPORT
Our main objective is to investigate subsurface processes governing the transport of PFAS from the RSVRA, and to integrate PFAS with other tracers to map the subsurface. The study uses PFAS data from 48 wells and a series of geochemical measurements for 25 wells, including major and trace elements, CFC and tritium age dating, and hydrogen and oxygen isotopes for tracing groundwater recharge. Spatial mapping of individual PFAS compounds indicates (A) that SSW flow is influenced by fractures and folded bedding, and (B) delineation of 4 potentially distinct PFAS groups, including, from source to downgradient: (1) proximal FTS-enriched waters; (2) water enriched in C4-C7 PFAS compounds; (3) water relatively enriched in C8 and C9 (PFOA, PFOS and PFNA); and (4) distal waters with below detection (BD) PFAS. Preliminary hydrogeochemical analysis indicates varied water types that may correspond to PFAS categories, from Ca-Mg-HCO3 waters with high PFAS to waters relatively enriched in K and SiO2 that have low or ND PFAS and are likely derived from distant recharge in the metamorphic rocks of the Green Mountains to the east. This is similar to the hydrogeology of PFOA contamination in a FRA in Bennington, VT, where upwelling K-Si-rich, PFAS-absent groundwater associated with intersecting fracture zones and thrust faults is compositionally distinct from the dominant carbonate signature. Mapping such heterogeneity is critical for predicting PFAS migration in the subsurface.