Abstract

A fourth of the global seabed sediment volume is buried at depths where temperatures exceed 80 °C, a previously proposed thermal barrier for life in the subsurface. Here, we demonstrate, utilizing an extensive suite of radiotracer experiments, the prevalence of active methanogenic and sulfate-reducing populations in deeply buried marine sediment from the Nankai Trough subduction zone, heated to extreme temperature (up to ~120 °C). The small microbial community subsisted with high potential cell-specific rates of energy metabolism, which approach the rates of active surface sediments and laboratory cultures. Our discovery is in stark contrast to the extremely low metabolic rates otherwise observed in the deep subseafloor. As cells appear to invest most of their energy to repair thermal cell damage in the hot sediment, they are forced to balance delicately between subsistence near the upper temperature limit for life and a rich supply of substrates and energy from thermally driven reactions of the sedimentary organic matter.

Highlights

  • A fourth of the global seabed sediment volume is buried at depths where temperatures exceed 80 °C, a previously proposed thermal barrier for life in the subsurface

  • Organic matter buried in the seabed provides a continuous supply of carbon and energy for microorganisms, allowing their subsistence in sediments that are more than 100 million years old[1] and buried as deep as ~2.5 km below the seafloor[2]

  • We demonstrate that a small community of microorganisms with rapid metabolism subsisted in the deep and hot, subseafloor biosphere

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Summary

Introduction

A fourth of the global seabed sediment volume is buried at depths where temperatures exceed 80 °C, a previously proposed thermal barrier for life in the subsurface. We performed highly sensitive radiotracer experiments, near the theoretical limit of detection, to measure potential rates of sulfate reduction (using 35S-SO42−) and methanogenesis (using 14C-dissolved inorganic carbon; DIC), and potential activity of anaerobic oxidation of methane (AOM, using 14C-CH4) in samples recovered from deep in the sediment column (for methodical details of all procedures see Methods and Supplementary Material).

Results
Conclusion

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