TY - JOUR
T1 - Extent and limits of biodegradation by in situ methanogenic consortia in shale and formation fluids
AU - Schlegel, Melissa E.
AU - McIntosh, Jennifer C.
AU - Petsch, Steven T.
AU - Orem, William H.
AU - Jones, Elizabeth J.P.
AU - Martini, Anna M.
N1 - Funding Information:
We thank the National Science Foundation (EAR-0635685J. McIntosh), the US Geological Survey, GTI and RPSEA through the “Ultra-Deepwater and Unconventional Natural Gas and Other Petroleum Resources” program for support of this research. In addition, we thank Joe Wade, Samuel Miller, Julian Damashek, and Daniel Kekacs for invaluable field help. Furthermore, we are grateful to Matthew Varonka (USGS) who provided the extractable hydrocarbon analysis of formation waters, Anne Bates (USGS) who analyzed formation waters for acetate, and Mark Woodworth who analyzed shale core samples. Finally, we express gratitude for the energy company personnel that allowed us access to their wells, and helped with sampling.
PY - 2013/1
Y1 - 2013/1
N2 - Consortia of microbes degrade recalcitrant organic-matter in deep subsurface reservoirs, such as shales and coals, under anaerobic conditions into simple C molecules such as CO2 and acetate. These substrates are subsequently metabolized by methanogens into economic quantities of natural gas in sedimentary basins world-wide. This study explores organic matter in the Devonian New Albany Shale (Illinois Basin, USA) and associated fluids to investigate the extent of organic matter biodegradation, and evaluate the potential for stimulating in situ gas production. Identification of labile compound classes such as n-alkanes, fatty acids, and phenols in produced waters of the New Albany Shale, and low biodegradation indices in the shale core samples indicate limited biodegradation. Together with detectable acetate concentrations (up to 225.1μM), these observations suggest that both the supporting microbial consortia and methanogens are limited in extent and activity. By comparison, the New Albany Shale is much less biodegraded than the microbial CH4-producing Michigan Basin Antrim Shale, Powder River Basin coals, or San Juan Basin coals. In the New Albany Shale, the extent of biodegradation generally becomes more varied with higher salinities, suggesting diverse microbial adaptations to degrade OM at high salinities. Enhancement of in situ CH4 production may be most effective if targeted at stimulating production of the supporting microbial consortia as well as methanogens.
AB - Consortia of microbes degrade recalcitrant organic-matter in deep subsurface reservoirs, such as shales and coals, under anaerobic conditions into simple C molecules such as CO2 and acetate. These substrates are subsequently metabolized by methanogens into economic quantities of natural gas in sedimentary basins world-wide. This study explores organic matter in the Devonian New Albany Shale (Illinois Basin, USA) and associated fluids to investigate the extent of organic matter biodegradation, and evaluate the potential for stimulating in situ gas production. Identification of labile compound classes such as n-alkanes, fatty acids, and phenols in produced waters of the New Albany Shale, and low biodegradation indices in the shale core samples indicate limited biodegradation. Together with detectable acetate concentrations (up to 225.1μM), these observations suggest that both the supporting microbial consortia and methanogens are limited in extent and activity. By comparison, the New Albany Shale is much less biodegraded than the microbial CH4-producing Michigan Basin Antrim Shale, Powder River Basin coals, or San Juan Basin coals. In the New Albany Shale, the extent of biodegradation generally becomes more varied with higher salinities, suggesting diverse microbial adaptations to degrade OM at high salinities. Enhancement of in situ CH4 production may be most effective if targeted at stimulating production of the supporting microbial consortia as well as methanogens.
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U2 - 10.1016/j.apgeochem.2012.10.008
DO - 10.1016/j.apgeochem.2012.10.008
M3 - Article
AN - SCOPUS:84871939301
SN - 0883-2927
VL - 28
SP - 172
EP - 184
JO - Applied Geochemistry
JF - Applied Geochemistry
ER -