Stephanie A. Napieralski, Yihang Fang, Virginia Marcon, Brandon Forsythe, Susan L. Brantley, Huifang Xu, Eric E. Roden
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Here, we assess the potential relevance of aerobic microbially catalyzed circumneutral pH pyrite oxidation in relation to subsurface shale weathering at Susquehanna Shale Hills Critical Zone Observatory (SSHCZO) in Pennsylvania, USA. Specimen pyrite mixed with native shale was incubated in groundwater for 3 months at the inferred depth of in situ pyrite oxidation. The colonized materials were used as an inoculum for pyrite-oxidizing enrichment cultures. Microbial activity accelerated the release of sulfate across all conditions. 16S rRNA gene sequencing and metagenomic analysis revealed the dominance of a putative chemolithoautotrophic sulfur-oxidizing bacterium from the genus <i>Thiobacillus</i> in the enrichment cultures. Previously proposed models for aerobic microbial pyrite oxidation were assessed in terms of physical constraints, enrichment culture geochemistry, and metagenomic analysis. 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引用次数: 3
摘要
黄铁矿的氧化风化作用在陆相环境中铁、硫的生物地球化学循环中起着重要作用。虽然酸性条件下生物加速黄铁矿氧化的机制和发生已经很好地确立,但对于微生物介导的黄铁矿氧化在环中性pH下的作用知之甚少。最近的研究(Percak-Dennett et al., 2017, Geobiology, 15,690)已经证明了有氧化能岩石营养微生物在环中性pH下加速黄铁矿氧化的能力,并提出了两种可能发生这种现象的机制模型。在这里,我们在美国宾夕法尼亚州的Susquehanna页岩山临界带观测站(SSHCZO)评估了好氧微生物催化的环中性pH黄铁矿氧化与地下页岩风化的潜在相关性。在推断黄铁矿原位氧化深度下,将黄铁矿样品与天然页岩混合在地下水中孵育3个月。定植的物质被用作黄铁矿氧化富集培养的接种物。微生物的活动加速了硫酸盐在所有条件下的释放。16S rRNA基因测序和宏基因组分析显示,来自硫杆菌属的一种推定的趋化石自养硫氧化细菌在富集培养中占主导地位。先前提出的好氧微生物黄铁矿氧化模型在物理约束、富集培养、地球化学和宏基因组分析方面进行了评估。尽管我们得出结论,SSCHZO的地下黄铁矿氧化在很大程度上是非生物的,但这项工作仍然对需氧微生物在环中性ph下加速黄铁矿氧化的潜在途径产生了新的见解。我们提出了一种新的“直接硫氧化”途径,即含巯基的外膜蛋白通过过硫中间体介导黄铁矿表面的氧化。类似于先前提出的直接微生物氧化单质硫的机制。这种和其他直接的微生物黄铁矿氧化途径的作用对控制环中性pH沉积环境中黄铁矿的风化速率具有重要意义,因为孔喉的大小允许微生物广泛进入黄铁矿表面。
Microbial chemolithotrophic oxidation of pyrite in a subsurface shale weathering environment: Geologic considerations and potential mechanisms
Oxidative weathering of pyrite plays an important role in the biogeochemical cycling of Fe and S in terrestrial environments. While the mechanism and occurrence of biologically accelerated pyrite oxidation under acidic conditions are well established, much less is known about microbially mediated pyrite oxidation at circumneutral pH. Recent work (Percak-Dennett et al., 2017, Geobiology, 15, 690) has demonstrated the ability of aerobic chemolithotrophic microorganisms to accelerate pyrite oxidation at circumneutral pH and proposed two mechanistic models by which this phenomenon might occur. Here, we assess the potential relevance of aerobic microbially catalyzed circumneutral pH pyrite oxidation in relation to subsurface shale weathering at Susquehanna Shale Hills Critical Zone Observatory (SSHCZO) in Pennsylvania, USA. Specimen pyrite mixed with native shale was incubated in groundwater for 3 months at the inferred depth of in situ pyrite oxidation. The colonized materials were used as an inoculum for pyrite-oxidizing enrichment cultures. Microbial activity accelerated the release of sulfate across all conditions. 16S rRNA gene sequencing and metagenomic analysis revealed the dominance of a putative chemolithoautotrophic sulfur-oxidizing bacterium from the genus Thiobacillus in the enrichment cultures. Previously proposed models for aerobic microbial pyrite oxidation were assessed in terms of physical constraints, enrichment culture geochemistry, and metagenomic analysis. Although we conclude that subsurface pyrite oxidation at SSCHZO is largely abiotic, this work nonetheless yields new insight into the potential pathways by which aerobic microorganisms may accelerate pyrite oxidation at circumneutral pH. We propose a new “direct sulfur oxidation” pathway, whereby sulfhydryl-bearing outer membrane proteins mediate oxidation of pyrite surfaces through a persulfide intermediate, analogous to previously proposed mechanisms for direct microbial oxidation of elemental sulfur. The action of this and other direct microbial pyrite oxidation pathways have major implications for controls on pyrite weathering rates in circumneutral pH sedimentary environments where pore throat sizes permit widespread access of microorganisms to pyrite surfaces.
期刊介绍:
The field of geobiology explores the relationship between life and the Earth''s physical and chemical environment. Geobiology, launched in 2003, aims to provide a natural home for geobiological research, allowing the cross-fertilization of critical ideas, and promoting cooperation and advancement in this emerging field. We also aim to provide you with a forum for the rapid publication of your results in an international journal of high standing. We are particularly interested in papers crossing disciplines and containing both geological and biological elements, emphasizing the co-evolutionary interactions between life and its physical environment over geological time.
Geobiology invites submission of high-quality articles in the following areas:
Origins and evolution of life
Co-evolution of the atmosphere, hydrosphere and biosphere
The sedimentary rock record and geobiology of critical intervals
Paleobiology and evolutionary ecology
Biogeochemistry and global elemental cycles
Microbe-mineral interactions
Biomarkers
Molecular ecology and phylogenetics.