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Sean R Scott

Publications and source records attributed to Sean R Scott.

3 recordsLinked to original sources

The dynamic influence of subsurface geological processes on the assembly and diversification of thermophilic microbial communities in continental hydrothermal systems

An accepted paradigm of hydrothermal systems is the process of phase separation, or boiling, of a deep, homogeneous hydrothermal fluid as it ascends through the subsurface resulting in gas rich and gas poor fluids. While phase separation helps to explain first-order patterns in the chemistry and biology of a hot spring’s surficial expression, we know little about the subsurface architecture beneath “phase-separated” pools and the timescales over which phase separation processes occur. Essentially, we have a two-dimensional understanding of a four-dimensional process. By combining geophysical, geochemical, isotopic, and microbiological measurements of two adjacent phase-separated hot springs in Norris Geyser Basin, Yellowstone National Park, we provide a four-dimensional assessment of phase separation processes and their biological manifestation. We uniquely show that Yellowstone’s hydrothermal waters originate from a deep sedimentary aquifer and that both meteoric recharge and shallow reactive transport processes are required to establish the geobiological feedbacks that drive bimodal distributions in the geochemical and microbial composition of hot springs. Specifically, over periods of tens of years, gas-enriched fluids containing volcanic sulfide mix with meteoric waters resulting in microbially-mediated production of sulfuric acid by thermoacidophilic Archaea in the near subsurface. In contrast, over periods of hundreds of years, anoxic residual liquid rises to the surface where it is infused with atmospheric gas fostering Archaea and Bacteria that are largely dependent on oxygen. As such, our results provide formative insight into the causative links between subsurface geological processes, the development of geochemical fluids, and the assembly and diversification of thermophilic microbial communities in hydrothermal systems.

Wyoming

Comparison of radium analytical methods for municipal drinking water well operation

Radium (Ra) is a geogenic contaminant that occurs at high levels in the Midwestern Cambrian-Ordovician aquifer system (MCOAS), a regionally important sandstone and carbonate drinking water aquifer. Water utilities using the MCOAS often must adopt treatment methods or use alternative water sources to maintain high-quality drinking water. Here, we show that Ra in water obtained from a municipal well in Wisconsin remains consistent despite variation in pumping conditions. However, widely used analytical methods (e.g., scintillation counting) for measuring Ra are less precise for quantifying Ra variability given the site conditions. Although not currently used for EPA compliance, mass spectrometry improves the precision of Ra measurements by an order of magnitude over the currently used counting method (e.g., 95 ± 3 mBq/L vs. 110 ± 30 mBq/L) at the concentrations observed in this study. The use of more precise analytical methods will increase understanding of trends in Ra levels important for operating public water systems.

Water Science and Engineering

Isotopic analysis of radium geochemistry at discrete intervals in the Midwestern Cambrian-Ordovician aquifer system

Radium (Ra) is a geogenic radioactive contaminant that frequently occurs at elevated levels in the Midwestern Cambrian-Ordovician aquifer system (MCOAS). Geochemical indicators (e.g., redox conditions or total dissolved solids) can broadly characterize conditions associated with elevated Ra levels in groundwater, but do not consistently correlate to elevated Ra within specific stratigraphic horizons. A coupled geochemical and isotopic study of groundwater and aquifer solids for major and trace elements, Ra, and uranium (U) at discrete intervals in the MCOAS was used to elucidate processes that may be responsible for this disconnect, via analysis of groundwater as well as extracted and digested solid aquifer samples. We find that the potential for Ra mobilization varies by stratigraphic unit, as observed by whole-rock 226 Ra/ 238 U (dis)equilibrium. Overall, the examined aqueous geochemical characteristics (e.g., redox conditions, total dissolved solids) do not explain Ra concentrations within the system, suggesting that alternative factors, like solid-phase associations or the extent of alpha recoil damage, may be more important. A relation between aqueous 87 Sr/ 86 Sr and 226 Ra suggests that minerals with radiogenic 87 Sr/ 86 Sr are more likely to release 226 Ra to the aqueous system. Overall, the release of U and Ra due to water-rock interaction varies with discrete stratigraphy, depending on aqueous geochemistry and available mineral associations. Due to complex Ra-rock interactions and the heterogeneous geology of the MCOAS, aqueous geochemistry does not fully predict the mobilization and concentration of Ra in groundwater. As sources and sinks of Ra within the MCOAS vary across stratigraphy, knowledge of aqueous geochemistry, available solid-phase associations, and nuclide leachability all are important to consider for understanding elevated Ra occurrence in aquifer systems.

Wisconsin