Hydrogen-Driven Microbial Redox Reactions in Deep Geosystems

Martin Krüger, Anja Dohrmann
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Abstract

In the subsurface, biotic and abiotic processes can generate and consume hydrogen. Hydrogen has a low reduction potential and is thus a highly energetic electron donor when involved in sulfate, carbon dioxide or ferric iron reduction. Although known as important drivers for the deep biosphere, the contributions of different processes to hydrogen turnover in different geosystems still are not well understood. In context with the ongoing transformation to renewable energy resources, underground H2 storage (UHS) in deep porous or salt cavern systems came into focus. In situ microbial and geochemical reactions that consume H2 are highly relevant topics in deep biosphere research, and also are still a major uncertainty during UHS. Consequently, we studied the potential microbial hydrogen oxidation rates – combined with the possible production of metabolic products like H2S, acetic acid or CH4 - in formation fluids from natural gas fields and salt caverns, thereby considering the importance of in situ pressure and temperature conditions, fluid chemistry and mineral composition. In addition, more defined experiments were conducted with selected pure cultures representing important metabolic groups of deep biosphere microorganisms. Several original formation fluids showed immediate H2 consumption. Microorganisms oxidized hydrogen at relevant in situ pressure conditions (up to 100 bar) and tolerated dynamically changing pressure and temperature conditions. The microbial hydrogen oxidation rate was strongly dependent on H2 partial pressures and the availability of e.g., sulfate as a terminal electron acceptor. High-throughput sequencing of 16S rRNA gene amplicons indicated hydrogen oxidation by sulfate reducing bacteria to be the presumed process in the studied porous rock reservoir fluids. In addition, hydrogen turnover by methanogenic and acetogenic as well as iron-reducing microorganisms was investigated. Also, the importance of biotic reactions in relation to abiotic hydrogen turnover processes at mineral surfaces will be discussed.
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深层地系中氢驱动的微生物氧化还原反应
在地下,生物和非生物过程可以产生和消耗氢。氢具有低还原电位,因此当参与硫酸盐、二氧化碳或铁还原时,氢是一个高能量的电子供体。尽管被认为是深层生物圈的重要驱动因素,但不同地球系统中不同过程对氢转换的贡献仍未得到很好的理解。在向可再生能源转型的背景下,深层多孔或盐穴系统中的地下氢气储存(UHS)成为人们关注的焦点。消耗h2的原位微生物和地球化学反应是深层生物圈研究中高度相关的主题,也是UHS研究中的主要不确定性。因此,我们研究了天然气田和盐洞地层流体中潜在的微生物氢氧化速率,并结合可能产生的代谢产物,如h2s、乙酸或ch4,从而考虑了原位压力和温度条件、流体化学和矿物组成的重要性。此外,选择代表深层生物圈微生物重要代谢群的纯培养物进行了更明确的实验。几种原始地层流体显示出立即的h2消耗。微生物在相关的原位压力条件下(高达100巴)氧化氢,并耐受动态变化的压力和温度条件。微生物的氢氧化速率强烈依赖于h2分压和硫酸盐作为终端电子受体的可用性。16S rRNA基因扩增子的高通量测序表明,硫酸盐还原菌在研究的多孔岩石储层流体中可能发生了氢氧化。此外,还研究了产甲烷微生物和产丙酮微生物以及铁还原微生物对氢的转化。此外,将讨论与矿物表面非生物氢周转过程有关的生物反应的重要性。
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