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Katherine Davis

Publications and source records attributed to Katherine Davis.

2 recordsLinked to original sources

Meso-scale pressure reactor demonstrates biostimulation of coal-dependent methanogenesis

Replicating deep subsurface conditions remains a major challenge for advancing subterranean biotechnologies. Microbially enhanced coal bed methane production offers a promising approach to increase biogenic gas recovery from coal seams, yet experimental progress has been limited by the difficulty of simulating in situ conditions. A key question is whether nutrient amendments stimulate coal-dependent methanogenesis or simply convert injected nutrients to methane. Here, we report the use of a large-scale (325 L) reactor to investigate 13 C-labeled microalgae amendments on microbially-enhanced coal bed methane production at in situ pressure. Labeled methane was detected only during the initial stimulation phase, while most of the methane produced over five months originated from the coal. These field-relevant results demonstrate that microalgae can accelerate early methanogenesis and enhance coal-derived methane production over time. This study provides a critical proof-of-concept with broad implications for advancing subsurface biotechnologies toward field-scale deployment.

Communications Earth & Environment

In situ enhancement and isotopic labeling of biogenic coalbed methane

Subsurface microbial (biogenic) methane production is an important part of the global carbon cycle that has resulted in natural gas accumulations in many coal beds worldwide. Laboratory studies suggest that complex carbon-containing nutrients (e.g., yeast or algae extract) can stimulate methane production, yet the effectiveness of these nutrients within coal beds is unknown. Here, we use downhole monitoring methods in combination with deuterated water (D 2 O) and a 200-liter injection of 0.1% yeast extract (YE) to stimulate and isotopically label newly generated methane. A total dissolved gas pressure sensor enabled real-time gas measurements (641 days preinjection and for 478 days postinjection). Downhole samples, collected with subsurface environmental samplers, indicate that methane increased 132% above preinjection levels based on isotopic labeling from D 2 O, 108% based on pressure readings, and 183% based on methane measurements 266 days postinjection. Demonstrating that YE enhances biogenic coalbed methane production in situ using multiple novel measurement methods has immediate implications for other field-scale biogenic methane investigations, including in situ methods to detect and track microbial activities related to the methanogenic turnover of recalcitrant carbon in the subsurface.

Montana