EXTREMOPHILES as Astrobiological Models. Группа авторов

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Schematic illustration of iron-oxidizing environment. Heated rainwater from magmatic heat convection produces steam that contacts lava and extracts soluble Fe(II). (1) Fe(II) is solubilized in the steam water and (2) rises with steam through porous lava fissures and cracks and reaches the iron vent openings of SW4, as the Fe(II) contacts air (3) Archaea utilize the Fe(II) in their growth by oxidizing the iron to Fe (III).

      Models of the sulfur and ammonia oxidizing environments are available in a previous study [1.3].

      The worldwide abundance of fumaroles compared to hot springs make this an ideal choice as a habitat for early development of life on Earth. These primitive steam habitats characterized by two extreme physical features, low pH and high temperature, typically flourish with Archaea. The fact that these organisms seem to have persisted from the earliest times argues that they may represent the type of living organism that could have evolved else-where beyond planet Earth. Steam caves/vents, while limited in diversity [1.7], represent and remain a rich and potentially useful and reliable source for isolation of unknown and unexplored life forms.

      1.1. Benson, C.A., Bizzoco, R.W., Lipson, D.A., Kelley, S.T., Microbial diversity in nonsulfur, sulfur and iron geothermal steam vents. FEMS Microbiol. Ecol., 76, 1, 74–88, 2011.

      1.2. Bizzoco, R.L.W. and Kelley, S.T., Microbial diversity in acidic high-temperature steam vents [Chapter 30], in: Polyextremophiles: Life under Multiple Forms of Stress [Volume 27 in the series: Cellular Origin, Life in Extreme Habitats and Astrobiology, series editor: Joseph Seckbach], J. Seckbach, A. Oren, H. Stan-Lotter (Eds.), pp. 315–332, Springer, Dordrecht, 2013.

      1.3. Bizzoco, R.L.W. and Kelley, S.T., Geothermal steam vents of Hawai’i [Chapter 2], in: Model Ecosystems in Extreme Environments [MEET], Volume 2 in the series: Astrobiology: Exploring Life on Earth and Beyond, P. Rampelotto, J. Seckbach, R. Gordon, J. Seckbach, P. Rampelotto (Eds.), pp. 23–40, Imperial College Press, UK, 2019.

      1.4. Brochier-Armanet, C., Boussau, B., Gribaldo, S., Forterre, P., Mesophilic crenarchaeota: Proposal for a third archaeal phylum, the Thaumarchaeota. Nat. Rev. Microbiol., 6, 3, 245– 252, 2008.

      1.5. Brock, T.D., Thermophilic Microorganisms and Life at High Temperatures, Springer, New York, 1978.

      1.6. Chemtob, S.M., Jolliff, B.L., Arvidson, R.E., Si-and Ti-rich surface coatings on Hawaiian basalt and implications for remote sensing on Mars, in: Lunar Planetary Science 37th Conference, 2006.

      1.7. Cockell, C.S., Harrison, J.P., Stevens, A.H., Payler, S.J., Hughes, S.S., Kobs Nawotniak, S.E., Brady, A.L., Elphic, R.C., Haberle, C.W. et al., A low-diversity microbiota inhabits extreme terrestrial basaltic terrains and their fumaroles: Implications for the exploration of Mars. Astrobiology, 19, 3, 284–299, 2019.

      1.8. Ellis, D.G., Bizzoco, R.W., Kelley, S.T., Halophilic Archaea determined from geothermal steam vent aerosols. Environ. Microbiol., 10, 6, 1582–1590, 2008.

      1.9. Grogan, D.W., Phenotypic characterization of the Archaebacterial genus Sulfolobus: Comparison of five wild-type strains. J. Bacteriol., 171, 12, 6710–6719, 1989.

      1.10. Hughes, S.S., Haberle, C.W., Kobs Nawotniak, S.E., Sehlke, A., Garry, W.B., Elphic, R.C., Payler, S.J., Stevens, A.H., Cockell, C.S., Brady, A.L. et al., Basaltic terrains in Idaho and Hawai’i as planetary analogs for Mars geology and astrobiology. Astrobiology, 19, 3, 260– 283, 2019.

      1.11. Jones, M.E., Ammonia equilibrium between vapor and liquid aqueous phases at elevated temperatures. J. Phys. Chem., 67, 5, 1113–1115, 1963.

      1.13. Nordstrom, D.K., Ball, J.W., McCleskey, R.B., Ground water to surface water: Chemistry of thermal outflows in Yellowstone National Park, in: Geothermal Biology and Geochemistry in Yellowstone National Park, W.P. Inskeep and T.R. McDermott (Eds.), pp. 73–94, Montana State University Publications, Bozeman, MT, 2005.

      1.14. Stahl, D.A. and de la Torre, J.R., Physiology and diversity of ammonia-oxidizing Archaea. Annu. Rev. Microbiol., 66, 83–101, 2012.

      1.15. Stieglmeier, M., Alves, R.J.E., Schleper, C., The Phylum Thaumarchaeota, in: The Prokaryotes, E. Rosenberg, E.F. DeLong, S. Lory, E. Stackebrandt, F. Thompson (Eds.), pp. 347–362, Springer-Verlag Berlin, Heidelberg,

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