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Microbial Communities in Subpermafrost Saline Fracture Water at the Lupin Au Mine, Nunavut, Canada
Authors:T C Onstott  Daniel J McGown  Corien Bakermans  Timo Ruskeeniemi  Lasse Ahonen  Jon Telling  Bruno Soffientino  Susan M Pfiffner  Barbara Sherwood-Lollar  Shaun Frape  Randy Stotler  Elizabeth J Johnson  Tatiana A Vishnivetskaya  Randi Rothmel  Lisa M Pratt
Institution:1. Department of Geosciences, Princeton University, Princeton, 08544, NJ, USA
2. Center for Microbial Ecology, Michigan State University, East Lansing, MI, USA
3. Geological Survey of Finland, Espoo, Finland
4. Earth Sciences Centre, University of Toronto, Toronto, ON, Canada
5. Graduate School of Oceanography, University of Rhode Island, Narragansett, RI, USA
6. Center for Environmental Biotechnology, The University of Tennessee, Knoxville, TN, USA
7. Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, ON, Canada
8. Department of Geological Sciences, Indiana University, Bloomington, IN, USA
11. Oak Ridge National Laboratory, Oak Ridge, TN, USA
9. Department of Food Science, North Carolina State University, Raleigh, NC, USA
10. Shaw Environmental Inc., Lawrenceville, NJ, USA
Abstract:We report the first investigation of a deep subpermafrost microbial ecosystem, a terrestrial analog for the Martian subsurface. Our multidisciplinary team analyzed fracture water collected at 890 and 1,130 m depths beneath a 540-m-thick permafrost layer at the Lupin Au mine (Nunavut, Canada). 14C, 3H, and noble gas isotope analyses suggest that the Na–Ca–Cl, suboxic, fracture water represents a mixture of geologically ancient brine, ~25-kyr-old, meteoric water and a minor modern talik-water component. Microbial planktonic concentrations were ~103 cells mL?1. Analysis of the 16S rRNA gene from extracted DNA and enrichment cultures revealed 42 unique operational taxonomic units in 11 genera with Desulfosporosinus, Halothiobacillus, and Pseudomonas representing the most prominent phylotypes and failed to detect Archaea. The abundance of terminally branched and midchain-branched saturated fatty acids (5 to 15 mol%) was consistent with the abundance of Gram-positive bacteria in the clone libraries. Geochemical data, the ubiquinone (UQ) abundance (3 to 11 mol%), and the presence of both aerobic and anaerobic bacteria indicated that the environment was suboxic, not anoxic. Stable sulfur isotope analyses of the fracture water detected the presence of microbial sulfate reduction, and analyses of the vein-filling pyrite indicated that it was in isotopic equilibrium with the dissolved sulfide. Free energy calculations revealed that sulfate reduction and sulfide oxidation via denitrification and not methanogenesis were the most thermodynamically viable consistent with the principal metabolisms inferred from the 16S rRNA community composition and with CH4 isotopic compositions. The sulfate-reducing bacteria most likely colonized the subsurface during the Pleistocene or earlier, whereas aerobic bacteria may have entered the fracture water networks either during deglaciation prior to permafrost formation 9,000 years ago or from the nearby talik through the hydrologic gradient created during mine dewatering. Although the absence of methanogens from this subsurface ecosystem is somewhat surprising, it may be attributable to an energy bottleneck that restricts their migration from surface permafrost deposits where they are frequently reported. These results have implications for the biological origin of CH4 on Mars.
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