ArticleMicrobial ecology2009
Microbial communities in subpermafrost saline fracture water at the Lupin Au mine, Nunavut, Canada.
Article in Microbial ecology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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Who cites it
17 citing papers in PubMed.
- Coupled C, H, N, S and Fe biogeochemical cycles operating in the continental deep subsurface of the Iberian Pyrite Belt.Environmental microbiology · 2023Article
- Microbial ecology of a shallow alkaline hydrothermal vent: Strýtan Hydrothermal Field, Eyjafördur, northern Iceland.Frontiers in microbiology · 2022Article
- In Situ Growth of Halophilic Bacteria in Saline Fracture Fluids from 2.4 km below Surface in the Deep Canadian Shield.Life (Basel, Switzerland) · 2020Article
- Paleo-Rock-Hosted Life on Earth and the Search on Mars: A Review and Strategy for Exploration.Astrobiology · 2019Review
- Exploring the piezotolerant/piezophilic microbial community and genomic basis of piezotolerance within the deep subsurface Deccan traps.Extremophiles : life under extreme conditions · 2019Article
- A Field Guide to Finding Fossils on Mars.Journal of geophysical research. Planets · 2018Review
- A thin ice layer segregates two distinct fungal communities in Antarctic brines from Tarn Flat (Northern Victoria Land).Scientific reports · 2018Article
- Isolation, Characterization, and Antibacterial Activity of Hard-to-Culture Actinobacteria from Cave Moonmilk Deposits.Antibiotics (Basel, Switzerland) · 2018Article
- Response of Deep Subsurface Microbial Community to Different Carbon Sources and Electron Acceptors during ∼2 months Incubation in Microcosms.Frontiers in microbiology · 2017Article
- Microbiome composition and geochemical characteristics of deep subsurface high-pressure environment, Pyhäsalmi mine Finland.Frontiers in microbiology · 2015Article
- The origin, source, and cycling of methane in deep crystalline rock biosphere.Frontiers in microbiology · 2015Review
- The transcriptional response of microbial communities in thawing Alaskan permafrost soils.Frontiers in microbiology · 2015Article
- Towards the selection of a produced water enrichment for biological gas hydrate inhibitors.Environmental science and pollution research international · 2014Article
- Taxonomically and functionally diverse microbial communities in deep crystalline rocks of the Fennoscandian shield.The ISME journal · 2014Article
- Microbial diversity and activity in hypersaline high Arctic spring channels.Extremophiles : life under extreme conditions · 2012Article
- Microbial and mineralogical characterizations of soils collected from the deep biosphere of the former Homestake gold mine, South Dakota.Microbial ecology · 2010Article
- Community structure of subsurface biofilms in the thermal sulfidic caves ofAcquasanta Terme, Italy.Applied and environmental microbiology · 2010Article
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Authors and funding
15 authors.
Funding
No grant is acknowledged in the PubMed record.
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, approximately25-kyr-old, meteoric water and a minor modern talik-water component. Microbial planktonic concentrations were approximately10(3) 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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