Department of Geological and Environmental Sciences, Ben Gurion University of the Negev, Beer-Sheva 84105, Israel;
Department of Earth Sciences, University of Cambridge, Cambridge CB2 3EQ, United Kingdom; and.
Proc Natl Acad Sci U S A. 2014 Oct 7;111(40):E4139-47. doi: 10.1073/pnas.1412269111. Epub 2014 Sep 22.
Seep sediments are dominated by intensive microbial sulfate reduction coupled to the anaerobic oxidation of methane (AOM). Through geochemical measurements of incubation experiments with methane seep sediments collected from Hydrate Ridge, we provide insight into the role of iron oxides in sulfate-driven AOM. Seep sediments incubated with (13)C-labeled methane showed co-occurring sulfate reduction, AOM, and methanogenesis. The isotope fractionation factors for sulfur and oxygen isotopes in sulfate were about 40‰ and 22‰, respectively, reinforcing the difference between microbial sulfate reduction in methane seeps versus other sedimentary environments (for example, sulfur isotope fractionation above 60‰ in sulfate reduction coupled to organic carbon oxidation or in diffusive sedimentary sulfate-methane transition zone). The addition of hematite to these microcosm experiments resulted in significant microbial iron reduction as well as enhancing sulfate-driven AOM. The magnitude of the isotope fractionation of sulfur and oxygen isotopes in sulfate from these incubations was lowered by about 50%, indicating the involvement of iron oxides during sulfate reduction in methane seeps. The similar relative change between the oxygen versus sulfur isotopes of sulfate in all experiments (with and without hematite addition) suggests that oxidized forms of iron, naturally present in the sediment incubations, were involved in sulfate reduction, with hematite addition increasing the sulfate recycling or the activity of sulfur-cycling microorganisms by about 40%. These results highlight a role for natural iron oxides during bacterial sulfate reduction in methane seeps not only as nutrient but also as stimulator of sulfur recycling.
渗漏沉积物主要由与甲烷厌氧氧化(AOM)相耦合的强烈微生物硫酸盐还原作用控制。通过对从 Hydrate Ridge 采集的甲烷渗漏沉积物进行培养实验的地球化学测量,我们深入了解了氧化铁在硫酸盐驱动的 AOM 中的作用。用(13)C 标记的甲烷培养的渗漏沉积物显示出同时发生的硫酸盐还原、AOM 和产甲烷作用。硫酸盐中硫和氧同位素的同位素分馏因子分别约为 40‰和 22‰,这加强了甲烷渗漏中微生物硫酸盐还原与其他沉积环境(例如,与有机碳氧化或扩散性沉积硫酸盐-甲烷过渡带中硫酸盐还原相关的硫同位素分馏高于 60‰)之间的差异。将赤铁矿添加到这些微宇宙实验中会导致微生物铁还原显著增强,同时促进硫酸盐驱动的 AOM。这些培养实验中硫酸盐中硫和氧同位素的同位素分馏幅度降低了约 50%,表明在甲烷渗漏中硫酸盐还原过程中涉及氧化铁。所有实验(有和没有赤铁矿添加)中硫酸盐的氧与硫同位素之间的相对变化相似,表明沉积物培养中天然存在的铁的氧化形式参与了硫酸盐还原,赤铁矿的添加使硫酸盐的再循环或硫循环微生物的活性增加了约 40%。这些结果强调了自然氧化铁在甲烷渗漏中细菌硫酸盐还原过程中的作用不仅是作为营养物质,而且还是作为硫循环刺激物。