Sulfur mass-independent fractionation in subsurface fracture waters indicates a long-standing sulfur cycle in Precambrian rocks

L. Li (), B. A. Wing, T. H. Bui, J. M. McDermott, G. F. Slater, S. Wei, G. Lacrampe-Couloume and B. Sherwood Lollar
Additional contact information
L. Li: University of Toronto
B. A. Wing: McGill University
T. H. Bui: McGill University
J. M. McDermott: University of Toronto
G. F. Slater: School of Geography and Earth Sciences, McMaster University
S. Wei: University of Alberta
G. Lacrampe-Couloume: University of Toronto
B. Sherwood Lollar: University of Toronto

Nature Communications, 2016, vol. 7, issue 1, 1-9

Abstract: Abstract The discovery of hydrogen-rich waters preserved below the Earth’s surface in Precambrian rocks worldwide expands our understanding of the habitability of the terrestrial subsurface. Many deep microbial ecosystems in these waters survive by coupling hydrogen oxidation to sulfate reduction. Hydrogen originates from water–rock reactions including serpentinization and radiolytic decomposition of water induced by decay of radioactive elements in the host rocks. The origin of dissolved sulfate, however, remains unknown. Here we report, from anoxic saline fracture waters ∼2.4 km below surface in the Canadian Shield, a sulfur mass-independent fractionation signal in dissolved sulfate. We demonstrate that this sulfate most likely originates from oxidation of sulfide minerals in the Archaean host rocks through the action of dissolved oxidants (for example, HO· and H2O2) themselves derived from radiolysis of water, thereby providing a coherent long-term mechanism capable of supplying both an essential electron donor (H2) and a complementary acceptor (sulfate) for the deep biosphere.

Date: 2016
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DOI: 10.1038/ncomms13252

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