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      Microbiology and Nitrogen Cycle in the Benthic Sediments of a Glacial Oligotrophic Deep Andean Lake as Analog of Ancient Martian Lake-Beds

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          Abstract

          Potential benthic habitats of early Mars lakes, probably oligotrophic, could range from hydrothermal to cold sediments. Dynamic processes in the water column (such as turbidity or UV penetration) as well as in the benthic bed (temperature gradients, turbation, or sedimentation rate) contribute to supply nutrients to a potential microbial ecosystem. High altitude, oligotrophic, and deep Andean lakes with active deglaciation processes and recent or past volcanic activity are natural models to assess the feasibility of life in other planetary lake/ocean environments and to develop technology for their exploration. We sampled the benthic sediments (down to 269 m depth) of the oligotrophic lake Laguna Negra (Central Andes, Chile) to investigate its ecosystem through geochemical, biomarker profiling, and molecular ecology studies. The chemistry of the benthic water was similar to the rest of the water column, except for variable amounts of ammonium (up to 2.8 ppm) and nitrate (up to 0.13 ppm). A life detector chip with a 300-antibody microarray revealed the presence of biomass in the form of exopolysaccharides and other microbial markers associated to several phylogenetic groups and potential microaerobic and anaerobic metabolisms such as nitrate reduction. DNA analyses showed that 27% of the Archaea sequences corresponded to a group of ammonia-oxidizing archaea (AOA) similar (97%) to Nitrosopumilus spp. and Nitrosoarchaeum spp. (Thaumarchaeota), and 4% of Bacteria sequences to nitrite-oxidizing bacteria from the Nitrospira genus, suggesting a coupling between ammonia and nitrite oxidation. Mesocosm experiments with the specific AOA inhibitor 2-Phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (PTIO) demonstrated an AOA-associated ammonia oxidation activity with the simultaneous accumulation of nitrate and sulfate. The results showed a rich benthic microbial community dominated by microaerobic and anaerobic metabolisms thriving under aphotic, low temperature (4°C), and relatively high pressure, that might be a suitable terrestrial analog of other planetary settings.

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          Ubiquity and diversity of ammonia-oxidizing archaea in water columns and sediments of the ocean.

          Nitrification, the microbial oxidation of ammonia to nitrite and nitrate, occurs in a wide variety of environments and plays a central role in the global nitrogen cycle. Catalyzed by the enzyme ammonia monooxygenase, the ability to oxidize ammonia was previously thought to be restricted to a few groups within the beta- and gamma-Proteobacteria. However, recent metagenomic studies have revealed the existence of unique ammonia monooxygenase alpha-subunit (amoA) genes derived from uncultivated, nonextremophilic Crenarchaeota. Here, we report molecular evidence for the widespread presence of ammonia-oxidizing archaea (AOA) in marine water columns and sediments. Using PCR primers designed to specifically target archaeal amoA, we find AOA to be pervasive in areas of the ocean that are critical for the global nitrogen cycle, including the base of the euphotic zone, suboxic water columns, and estuarine and coastal sediments. Diverse and distinct AOA communities are associated with each of these habitats, with little overlap between water columns and sediments. Within marine sediments, most AOA sequences are unique to individual sampling locations, whereas a small number of sequences are evidently cosmopolitan in distribution. Considering the abundance of nonextremophilic archaea in the ocean, our results suggest that AOA may play a significant, but previously unrecognized, role in the global nitrogen cycle.
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            Organic molecules in the Sheepbed Mudstone, Gale Crater, Mars

            The Sample Analysis at Mars (SAM) instrument on board the Mars Science Laboratory Curiosity rover is designed to conduct inorganic and organic chemical analyses of the atmosphere and the surface regolith and rocks to help evaluate the past and present habitability potential of Mars at Gale Crater. Central to this task is the development of an inventory of any organic molecules present to elucidate processes associated with their origin, diagenesis, concentration, and long-term preservation. This will guide the future search for biosignatures. Here we report the definitive identification of chlorobenzene (150–300 parts per billion by weight (ppbw)) and C2 to C4 dichloroalkanes (up to 70 ppbw) with the SAM gas chromatograph mass spectrometer (GCMS) and detection of chlorobenzene in the direct evolved gas analysis (EGA) mode, in multiple portions of the fines from the Cumberland drill hole in the Sheepbed mudstone at Yellowknife Bay. When combined with GCMS and EGA data from multiple scooped and drilled samples, blank runs, and supporting laboratory analog studies, the elevated levels of chlorobenzene and the dichloroalkanes cannot be solely explained by instrument background sources known to be present in SAM. We conclude that these chlorinated hydrocarbons are the reaction products of Martian chlorine and organic carbon derived from Martian sources (e.g., igneous, hydrothermal, atmospheric, or biological) or exogenous sources such as meteorites, comets, or interplanetary dust particles. Key Points First in situ evidence of nonterrestrial organics in Martian surface sediments Chlorinated hydrocarbons identified in the Sheepbed mudstone by SAM Organics preserved in sample exposed to ionizing radiation and oxidative condition
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              Organic matter preserved in 3-billion-year-old mudstones at Gale crater, Mars

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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                03 May 2019
                2019
                : 10
                : 929
                Affiliations
                [1] 1Centro de Astrobiología (CSIC-INTA) , Madrid, Spain
                [2] 2SETI Institute, Carl Sagan Center , Mountain View, CA, United States
                [3] 3NASA Ames Research Center , Mountain View, CA, United States
                [4] 4Campoalto Operaciones SpA , Santiago, Chile
                [5] 5Instituto Español de Oceanografía (IEO) , Málaga, Spain
                [6] 6Muséum National d’Histoire Naturelle , Paris, France
                [7] 7School of Environmental Sciences, University of Guelph , Guelph, ON, Canada
                [8] 8Centro de Biotecnología, Universidad Católica del Norte , Antofagasta, Chile
                [9] 9Vicerrectoría de Investigación y Postgrado, Universidad Católica del Maule , Talca, Chile
                [10] 10Department of Natural Resource Sciences, McGill University , Montreal, QC, Canada
                [11] 11Department of Astronomy, Cornell University , Ithaca, NY, United States
                Author notes

                Edited by: Mónica Sánchez-Román, VU University Amsterdam, Netherlands

                Reviewed by: Kathryn Coyne, University of Delaware, United States; Camille Thomas, Université de Genève, Switzerland; Jeffrey M. Dick, Central South University, China

                *Correspondence: Victor Parro, parrogv@ 123456cab.inta-csic.es

                Present address: Fernando Puente-Sánchez, Systems Biology Program, CNB-CSIC, Madrid, Spain

                This article was submitted to Microbiological Chemistry and Geomicrobiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2019.00929
                6509559
                31130930
                0aad5706-30b0-481f-ab59-4e52d2932449
                Copyright © 2019 Parro, Puente-Sánchez, Cabrol, Gallardo-Carreño, Moreno-Paz, Blanco, García-Villadangos, Tambley, Tilot, Thompson, Smith, Sobrón, Demergasso, Echeverría-Vega, Fernández-Martínez, Whyte and Fairén.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 30 July 2018
                : 12 April 2019
                Page count
                Figures: 6, Tables: 0, Equations: 0, References: 68, Pages: 14, Words: 0
                Funding
                Funded by: Ministerio de Economía, Industria y Competitividad, Gobierno de España 10.13039/501100010198
                Funded by: National Aeronautics and Space Administration 10.13039/100000104
                Funded by: H2020 European Research Council 10.13039/100010663
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                microbiology of deep benthic habitats,andean lakes,deglaciation,ammonia oxidation,nitrification-denitrification,benthic sediments,planetary exploration,planetary lakes

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