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Colin P. Thackray

Publications and source records attributed to Colin P. Thackray.

3 recordsLinked to original sources

Centurial persistence of forever chemicals at military fire training sites

Drinking water contamination by per- and polyfluoroalkyl substances (PFAS) is widespread near more than 300 United States (U.S.) military bases that used aqueous film-forming foams (AFFF) for fire training and firefighting activities. Much of the PFAS at these sites consist of precursors that can transform into terminal compounds of known health concern but are omitted from standard analytical methods. Here, we estimate the expected duration and contribution of precursor biotransformation to groundwater PFAS contamination at an AFFF-contaminated military base on Cape Cod, Massachusetts, United States, by optimizing a geochemical box model using measured PFAS concentrations from a multidecadal time series of groundwater and a soil survey in the source zone. A toolbox of analytical techniques used to reconstruct the mass budget of PFAS showed that precursors accounted for 46 ± 8% of the extractable organofluorine (a proxy for total PFAS) across years. Terminal PFAS still exceed regulatory limits by 2000-fold decades after AFFF use ceased. Measurements and numerical modeling show that sulfonamido precursors are retained in the vadose zone and their slow biotransformation into perfluoroalkyl sulfonates (half-life > 66 yr) sustains groundwater concentrations of perfluorobutane sulfonate (PFBS) and perfluorohexane sulfonate (PFHxS). The estimated PFAS reservoir in the vadose zone and modeled flux into groundwater suggest PFAS contamination above regulatory guidelines will persist for centuries without remediation.

Massachusetts↗

Mercury in soils of the conterminous United States: Patterns and pools

Soils account for the largest global mercury reservoirs, but observations are sparse in many regions. The accumulation and turnover of mercury in soils determines whether they act as an atmospheric source or sink. Here, we present a spatial analysis of soil mercury from a large soil survey (three horizons, ∼4800 sites) across the conterminous United States conducted by the U.S. Geological Survey. Soil mercury pools were calculated for 11 layers, cumulatively representing the top 1 m of soil, and totaling 158 ± 2 Gg (±SD) of mercury (20.3 ± 0.2 mg m −2 ). Mercury areal density was greatest in mixed forest (27.3 ± 0.5 mg m −2 ), cropland (25.3 ± 0.3 mg m −2 ), and deciduous forest (25.6 ± 0.5 mg m −2 ) ecosystems and lowest in barren (13.5 ± 0.3 mg m −2 ) and shrubland (12.6 ± 0.2 mg m −2 ) ecosystems. Assessment of the provenance of soil mercury using bedrock titanium normalization suggests that 62%–95% of soil mercury is unexplained by parental sources.

conterminous United States↗

Isolating the AFFF signature in coastal watersheds using oxidizable PFAS precursors and unexplained organofluorine

Water supplies for millions of U.S. individuals exceed maximum contaminant levels for per- and polyfluoroalkyl substances (PFAS). Contemporary and legacy use of aqueous film forming foams (AFFF) is a major contamination source. However, diverse PFAS sources are present within watersheds, making it difficult to isolate their predominant origins. Here we examine PFAS source signatures among six adjacent coastal watersheds on Cape Cod, MA, U.S.A. using multivariate clustering techniques. A distinct signature of AFFF contamination enriched in precursors with six perfluorinated carbons (C6) was identified in watersheds with an AFFF source, while others were enriched in C4 precursors. Principal component analysis of PFAS composition in impacted watersheds showed a decline in precursor composition relative to AFFF stocks and a corresponding increase in terminal perfluoroalkyl sulfonates with < C6 but not those with ≥ C6. Prior work shows that in AFFF stocks, all extractable organofluorine (EOF) can be explained by targeted PFAS and precursors inferred using Bayesian inference on the total oxidizable precursor assay. Using the same techniques for the first time in impacted watersheds, we find that only 24%–63% of the EOF can be explained by targeted PFAS and oxidizable precursors. Our work thus indicates the presence of large non-AFFF organofluorine sources in these coastal watersheds.

Massachusetts↗