Abstract

The majority of anaerobic biogeochemical cycling occurs within marine sediments. To understand these processes, quantifying the distribution of active cells and gross metabolic activity is essential. We present an isotope model rooted in thermodynamics to draw quantitative links between cell-specific sulfate reduction rates and active sedimentary cell abundances. This model is calibrated using data from a series of continuous culture experiments with two strains of sulfate reducing bacteria (freshwater bacterium Desulfovibrio vulgaris strain Hildenborough, and marine bacterium Desulfovibrio alaskensis strain G-20) grown on lactate across a range of metabolic rates and ambient sulfate concentrations. We use a combination of experimental sulfate oxygen isotope data and nonlinear regression fitting tools to solve for unknown kinetic, step-specific oxygen isotope effects. This approach enables identification of key isotopic reactions within the metabolic pathway, and defines a new, calibrated framework for understanding oxygen isotope variability in sulfate. This approach is then combined with porewater sulfate/sulfide concentration data and diagenetic modeling to reproduce measured 18O/16O in porewater sulfate. From here, we infer cell-specific sulfate reduction rates and predict abundance of active cells of sulfate reducing bacteria, the result of which is consistent with direct biological measurements.

Highlights

  • A significant fraction of biogeochemical cycling takes place within marine sediments and is driven by microbial activity [1, 2]

  • In what follows we demonstrate that the oxygen isotopic composition of porewater sulfate tracks the abundance of active sulfate reducing bacteria in sediments

  • This work suggests that the microbial sulfate reduction (MSR) oxygen isotopic signature can be used to infer the abundance of active cells in marine sediments

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Summary

Introduction

A significant fraction of biogeochemical cycling takes place within marine sediments and is driven by microbial activity [1, 2]. Cell-specific metabolic rates can be inferred via the inorganic chemical signatures of that activity One such example, and central to this study, are the laboratory calibrated stable isotope effects associated with microbial sulfate reduction (MSR) [11, 12]. We show the sulfate oxygen isotopic composition in porewaters (Panel a) and pure cultures (Panel b) undergoing active MSR, and highlights the role of sulfate reduction rates in the development of this oxygen isotopic signature This interpretation has been extended to include the biochemistry of MSR and its specific role in modern marine environments, highlighting the potential of sulfate oxygen isotopic compositions to refine paleoenvironmental reconstructions [19, 21, 23,24,25,26,27,28,29,30]. Implicit in this new approach is isolating the reductive and oxidative fluxes within the MSR biochemistry

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