Abstract

Iron reduction and sulfate reduction are two of the major biogeochemical processes that occur in anoxic sediments. Microbes that catalyze these reactions are therefore some of the most abundant organisms in the subsurface, and some of the most important. Due to the variety of mechanisms that microbes employ to derive energy from these reactions, including the use of soluble electron shuttles, the dynamics between iron- and sulfate-reducing populations under changing biogeochemical conditions still elude complete characterization. Here, we amended experimental bioreactors comprised of freshwater aquifer sediment with ferric iron, sulfate, acetate, and the model electron shuttle AQDS (9,10-anthraquinone-2,6-disulfonate) and monitored both the changing redox conditions as well as changes in the microbial community over time. The addition of the electron shuttle AQDS did increase the initial rate of FeIII reduction; however, it had little effect on the composition of the microbial community. Our results show that in both AQDS- and AQDS+ systems there was an initial dominance of organisms classified as Geobacter (a genus of dissimilatory FeIII-reducing bacteria), after which sequences classified as Desulfosporosinus (a genus of dissimilatory sulfate-reducing bacteria) came to dominate both experimental systems. Furthermore, most of the ferric iron reduction occurred under this later, ostensibly “sulfate-reducing” phase of the experiment. This calls into question the usefulness of classifying subsurface sediments by the dominant microbial process alone because of their interrelated biogeochemical consequences. To better inform models of microbially-catalyzed subsurface processes, such interactions must be more thoroughly understood under a broad range of conditions.

Highlights

  • The biogeochemical cycling of carbon (C), iron (Fe), and sulfur (S) in aquatic and terrestrial environments is driven largely by microbially-catalyzed redox reactions

  • We investigate the effects of the presence and absence of a soluble electron shuttle (AQDS) on biogeochemical dynamics and microbial community development under FeIII- and sulfate-reducing conditions

  • FeIII was provided as natural sienna (Earth Pigments Co.), an iron-rich earth mined from ochre deposits in the Provence region of France that consists primarily of quartz and goethite (α-FeOOH), as determined by powder x-ray diffraction and Fe K-edge extended x-ray absorption fine-structure (EXAFS) spectroscopy

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Summary

Introduction

The biogeochemical cycling of carbon (C), iron (Fe), and sulfur (S) in aquatic and terrestrial environments is driven largely by microbially-catalyzed redox reactions. In many environments ferric iron (FeIII) is primarily present as relatively insoluble FeIII oxides These minerals provide an important electron sink during anaerobic respiration by a variety of dissimilatory FeIII-reducing bacteria (DIRB) and archaea. These phylogenetically diverse microorganisms are able to obtain energy by coupling the oxidation of organic compounds or molecular hydrogen to the reduction of FeIII to FeII under suboxic and anoxic conditions [1,2,3]. FeIII-reducing microorganisms and the reactive ferrous species they produce play a major role in controlling water quality [4,5], the dissolution and precipitation of minerals [6,7,8], nutrient availability [9], and the fate and transport of contaminants [10]

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