PROCESSES GOVERNING DISTRIBUTION OF AFFF-DERIVED PFAS IN A FRACTURED CARBONATE AQUIFER, WEST-CENTRAL VERMONT, USA
Mapping of groundwater composition indicates 3 general categories: (1) proximal to source fluorotelomer sulfonate-enriched waters (up to 600 ng/L PFAS); (2) farther down gradient (0.5 – 2 km) groundwater relatively enriched in C4-C9 carboxylic acid PFAS (e.g. PFBA, PFHxA, PFOA, PFOS and PFNA and others up to 73 ng/L PFAS);(3) distal waters (> 2.5 km) with no detectable PFAS (< 2 ng/L). Within these categories, PFAS occurrence is highly heterogeneous, suggesting transport along bedrock structures (e.g. bedding and fracture planes). Locally-upwelling groundwater derived from the Green Mountains – with anomalous chemical signatures (low Ca-Mg-HCO3) and relatively old recharge ages (> 45 y) – provides PFAS-free water to localized compartments of the carbonate aquifer. Concentrations of the carboxylic acid PFAS compounds co-vary in the aquifer system whereas sulfonate PFAS compounds do not correlate with other sulfonates, nor with carboxylic acid PFAS. Extent of PFAS distribution suggests groundwater flow ~ 50-70 m/yr.
Surface mapping, drone photogrammetry, and geophysical logging reveal that bedding, foliations, fractures, and fold structures influence PFAS migration, individually or in combination. Conspicuous, steeply dipping, ~ N-S and E-W striking fracture zones that intersect could explain the apparent southwest stepping migration of PFAS from the point source area. Ongoing work will integrate the chemical and bedrock data into a 3D conceptual model.