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Using Flexible Gold-Titanium Reaction Cells to Simulate Pressure-Dependent Microbial Activity in the Context of Subsurface Biomining
Published on: October 5, 2019
Microbial carbonate biomineralization in the deep subsurface biosphere: Decoding long-term carbon sequestration
Ashiq Hussain1, Suprokash Koner2, Danish Ali1
1Department of Earth and Environmental Sciences, National Chung Cheng University, Chiayi County, Taiwan; Doctoral Program in Science, Technology, Environment, and Mathematics, National Chung Cheng University, Chiayi County, Taiwan.
None:
Geological carbon sequestration represents a cornerstone mitigation strategy for stabilizing atmospheric carbon dioxide (CO2) concentrations and limiting climate impacts from anthropogenic emissions. Its long-term effectiveness depends on geochemical and biological processes within deep subsurface environments, where microbial activity regulates CO2 transformation and stability. Among these processes, calcium carbonate biomineralization and methanogenesis are particularly important because they modify pH, alkalinity, redox conditions, and the availability of divalent cations, thereby promoting carbonate mineral precipitation and influencing the fate of injected CO2. Within the deep subsurface biosphere, microbial communities interact with porous media where pore architecture, fluid flow, and geochemical gradients strongly influence metabolic activity and biomineralization potential. Microbial carbonate precipitation in these environments is associated with anaerobic pathways such as sulfate reduction, urea hydrolysis, and anaerobic methane oxidation, which generate alkalinity and bicarbonate and create conditions favorable for calcium carbonate (CaCO3) formation. These microbial pathways, together with other carbon-transforming processes such as methanogenesis, acetogenesis, and fermentation, collectively shape carbonate formation within the subsurface carbon cycle and influence whether CO2 is ultimately retained as mineral carbonates or converted into methane. However, injection of high CO2 concentrations can shift subsurface pH, redox potential, and ionic strength, disrupting biomineralization and enhancing methanogenesis. These perturbations reshape pore-scale carbon dynamics and increase the risk of CO2 release as methane, underscoring microbial-geochemical interactions as fundamental controls on long-term carbon sequestration outcomes. This review highlights the role of coupled microbial pathways and geolocial conditions in shaping the fate of CO2, reinforcing their broader significance for ensuring the long-term effectiveness of carbon storage as a climate change mitigation strategy.
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