Download

Full Text

46

CITATIONS

46 Total citations

14 Recent citations

8.52 Field Citation Ratio

1.03 Relative Citation Ratio

publications

0

supporting

0

mentioning

0

contrasting

0

Smart Citations

0

0

0

0

Citing PublicationsSupportingMentioningContrasting

View Citations

See how this article has been cited at scite.ai

scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

• Bell, E.A.; Boehnke, P.; Harrison, T.M.; Mao,W.L. Potentially biogenic carbon preserved in a 4.1 billion-year-old zircon. Proc. Natl. Acad. Sci. USA 2015, 112, 14518-14521. [CrossRef] [PubMed]
• Javaux, E.J.; Marshall, C.P.; Bekker, A. Organic-walled microfossils in 3.2-billion-year-old shallow-marine siliciclastic deposits. Nature 2010, 463, 934-938. [CrossRef] [PubMed]
• Nutman, A.P.; Bennett, V.C.; Friend, C.R.; Van Kranendonk, M.J.; Chivas, A.R. Rapid emergence of life shown by discovery of 3700-million-year-old microbial structures. Nature 2016, 537, 535-538. [CrossRef] [PubMed]
• Wacey, D.; Kilburn, M.R.; Saunders, M.; Cliff, J.; Brasier, M.D. Microfossils of sulfur-metabolizing cells in 3.4-billion-year-old rocks ofWestern Australia. Nat. Geosci. 2011, 4, 698-702. [CrossRef]
• Di Giulio, M. The universal ancestor and the ancestor of bacteria were hyperthermophiles. J. Mol. Evol. 2003, 57, 721-730. [CrossRef] [PubMed]
• Stetter, K.O. Hyperthermophiles in the history of life. Ciba Found. Symp. 1996, 202, 1-10. [PubMed]
• Raymann, K.; Brochier-Armanet, C.; Gribaldo, S. The two-domain tree of life is linked to a new root for the Archaea. Proc. Natl. Acad. Sci. USA 2015, 112, 6670-6675. [CrossRef] [PubMed]
• Williams, T.A.; Foster, P.G.; Cox, C.J.; Embley, T.M. An archaeal origin of eukaryotes supports only two primary domains of life. Nature 2013, 504, 231-236. [CrossRef] [PubMed]
• Zaremba-Niedzwiedzka, K.; Caceres, E.F.; Saw, J.H.; Backstrom, D.; Juzokaite, L.; Vancaester, E.; Seitz, K.W.; Anantharaman, K.; Starnawski, P.; Kjeldsen, K.U.; et al. Asgard archaea illuminate the origin of eukaryotic cellular complexity. Nature 2017, 541, 353-358. [CrossRef] [PubMed]
• Cavicchioli, R. Archaea-timeline of the third domain. Nat. Rev. Microbiol. 2011, 9, 51-61. [CrossRef] [PubMed]
• Galtier, N.; Tourasse, N.; Gouy, M. A nonhyperthermophilic common ancestor to extant life forms. Science 1999, 283, 220-221. [CrossRef] [PubMed]
• Miller, S.L.; Lazcano, A. The origin of life-did it occur at high temperatures? J. Mol. Evol. 1995, 41, 689-692. [CrossRef] [PubMed]
• Boussau, B.; Blanquart, S.; Necsulea, A.; Lartillot, N.; Gouy, M. Parallel adaptations to high temperatures in the Archaean eon. Nature 2008, 456, 942-945. [CrossRef] [PubMed]
• Brochier, C.; Philippe, H. A non-hyperthermophilic ancestor for bacteria. Nature 2002, 417, 244. [CrossRef] [PubMed]
• Glansdorff, N.; Xu, Y.; Labedan, B. The last universal common ancestor: Emergence, constitution and genetic legacy of an elusive forerunner. Biol. Direct 2008, 3, 29. [CrossRef] [PubMed]
• Xu, Y.; Glansdorff, N. Was our ancestor a hyperthermophilic procaryote? Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2002, 133, 677-688. [CrossRef]
• McDermott, J.M.; Seewald, J.S.; German, C.R.; Sylva, S.P. Pathways for abiotic organic synthesis at submarine hydrothermal fields. Proc. Natl. Acad. Sci. USA 2015, 112, 7668-7672. [CrossRef] [PubMed]
• Weiss, M.C.; Sousa, F.L.; Mrnjavac, N.; Neukirchen, S.; Roettger, M.; Nelson-Sathi, S.; Martin, W.F. The physiology and habitat of the last universal common ancestor. Nat. Microbiol. 2016, 1, 16116. [CrossRef] [PubMed]
• Daniel, I.; Oger, P.; Winter, R. Origins of life and biochemistry under high-pressure conditions. Chem. Soc. Rev.2006, 35, 858-875. [CrossRef] [PubMed]
• Dodd, M.S.; Papineau, D.; Grenne, T.; Slack, J.F.; Rittner, M.; Pirajno, F.; O’Neil, J.; Little, C.T. Evidence for early life in Earth’s oldest hydrothermal vent precipitates. Nature 2017, 543, 60-64. [CrossRef] [PubMed]
• Sankaran, N. The RNA world at thirty: A look back with its author. J. Mol. Evol. 2016, 83, 169-175. [CrossRef] [PubMed]
• Gilbert, W. The RNA world. Nature 1986, 319, 618. [CrossRef]
• Levy, M.; Miller, S.L. The stability of the RNA bases: Implications for the origin of life. Proc. Natl. Acad. Sci. USA 1998, 95, 7933-7938. [CrossRef] [PubMed]
• Lambert, J.F.; Sodupe, M.; Ugliengo, P. Prebiotic chemistry. Chem. Soc. Rev. 2012, 41, 5373-5374. [CrossRef] [PubMed]
• Jheeta, S. The landscape of the emergence of Life. Life 2016, 6, 20. [CrossRef] [PubMed]
• Rodrigues, D.F.; Tiedje, J.M. Coping with our cold planet. Appl. Environ. Microbiol. 2008, 74, 1677-1686. [CrossRef] [PubMed]
• Margesin, R.; Schinner, F.; Marx, J.C.; Gerday, C. Psychrophiles, from Biodiversity to Biotechnology; Springer:Berlin/Heidelberg, Germany, 2008; p. 462.
• Cavicchioli, R. On the concept of a psychrophile. ISME J. 2016, 10, 793-795. [CrossRef] [PubMed]
• Feller, G.; Gerday, C. Psychrophilic enzymes: Hot topics in cold adaptation. Nat. Rev. Microbiol. 2003, 1, 200-208. [CrossRef] [PubMed]
• Steven, B.; Leveille, R.; Pollard, W.H.; Whyte, L.G. Microbial ecology and biodiversity in permafrost. Extremophiles 2006, 10, 259-267. [CrossRef] [PubMed]
• Deming, J.W. Psychrophiles and polar regions. Curr. Opin. Microbiol. 2002, 5, 301-309. [CrossRef]
• Junge, K.; Eicken, H.; Deming, J.W. Bacterial activity at -2 to -20°C in Arctic wintertime sea ice. Appl. Environ. Microbiol. 2004, 70, 550-557. [CrossRef] [PubMed]
• Vaitilingom, M.; Amato, P.; Sancelme, M.; Laj, P.; Leriche, M.; Delort, A.M. Contribution of microbial activity to carbon chemistry in clouds. Appl. Environ. Microbiol. 2010, 76, 23-29. [CrossRef] [PubMed]
• Mykytczuk, N.C.; Foote, S.J.; Omelon, C.R.; Southam, G.; Greer, C.W.; Whyte, L.G. Bacterial growth at -15°C; molecular insights from the permafrost bacterium Planococcus halocryophilus Or1. ISME J. 2013, 7, 1211-1226. [CrossRef] [PubMed]
• Cary, S.C.; McDonald, I.R.; Barrett, J.E.; Cowan, D.A. On the rocks: The microbiology of Antarctic Dry Valley soils. Nat. Rev. Microbiol. 2010, 8, 129-138. [CrossRef] [PubMed]
• Cameron, K.A.; Hodson, A.J.; Osborn, A.M. Structure and diversity of bacterial, eukaryotic and archaeal communities in glacial cryoconite holes from the Arctic and the Antarctic. FEMS Microbiol. Ecol. 2012, 82, 254-267. [CrossRef] [PubMed]
• Selbmann, L.; Zucconi, L.; Isola, D.; Onofri, S. Rock black fungi: Excellence in the extremes, from the Antarctic to space. Curr. Genet. 2015, 61, 335-345. [CrossRef] [PubMed]
• Giordano, D.; Russo, R.; di Prisco, G.; Verde, C. Molecular adaptations in Antarctic fish and marine microorganisms. Mar. Genom. 2012, 6, 1-6. [CrossRef] [PubMed]
• Roman Dial, C.; Dial, R.J.; Saunders, R.; Lang, S.A.; Lee, B.;Wimberger, P.; Dinapoli, M.S.; Egiazarov, A.S.; Gipple, S.L.; Maghirang, M.R.; et al. Historical biogeography of the North American glacier ice worm, Mesenchytraeus solifugus (Annelida: Oligochaeta: Enchytraeidae). Mol. Phylogenet. Evol. 2012, 63, 577-584. [CrossRef] [PubMed]
• D’Amico, S.; Collins, T.; Marx, J.C.; Feller, G.; Gerday, C. Psychrophilic microorganisms: Challenges for life. EMBO Rep. 2006, 7, 385-389. [CrossRef] [PubMed]
• Feller, G. Psychrophilic enzymes: From folding to function and biotechnology. Scientifica 2013, 512840. [CrossRef] [PubMed]
• Zecchinon, L.; Claverie, P.; Collins, T.; D’Amico, S.; Delille, D.; Feller, G.; Georlette, D.; Gratia, E.; Hoyoux, A.; Meuwis, M.A.; et al. Did psychrophilic enzymes really win the challenge? Extremophiles 2001, 5, 313-321. [CrossRef] [PubMed]
• Johnson, S.S.; Hebsgaard, M.B.; Christensen, T.R.; Mastepanov, M.; Nielsen, R.; Munch, K.; Brand, T.; Gilbert, M.T.; Zuber, M.T.; Bunce, M.; et al. Ancient bacteria show evidence of DNA repair. Proc. Natl. Acad. Sci. USA 2007, 104, 14401-14405. [CrossRef] [PubMed]
• Priscu, J.C.; Christtner, B.C. Earth’s icy biosphere. In Microbial Diversity and Bioprospecting; Bull, A.T., Ed.; ASM Press: Washington, DC, USA, 2004; pp. 130-145.
• Elster, J.; Margesin, R.; Wagner, D.; Haggblom, M. Polar and Alpine Microbiology-Earth’s Cryobiosphere. FEMS Microbiol. Ecol. 2016, 93. [CrossRef] [PubMed]
• Boetius, A.; Anesio, A.M.; Deming, J.W.; Mikucki, J.A.; Rapp, J.Z. Microbial ecology of the cryosphere: Sea ice and glacial habitats. Nat. Rev. Microbiol. 2015, 13, 677-690. [CrossRef] [PubMed]
• Cavicchioli, R. Microbial ecology of Antarctic aquatic systems. Nat. Rev. Microbiol. 2015, 13, 691-706. [CrossRef] [PubMed]
• De Maayer, P.; Anderson, D.; Cary, C.; Cowan, D.A. Some like it cold: Understanding the survival strategies of psychrophiles. EMBO Rep. 2014, 15, 508-517. [CrossRef] [PubMed]
• Hultman, J.; Waldrop, M.P.; Mackelprang, R.; David, M.M.; McFarland, J.; Blazewicz, S.J.; Harden, J.; Turetsky, M.R.; McGuire, A.D.; Shah, M.B.; et al. Multi-omics of permafrost, active layer and thermokarst bog soil microbiomes. Nature 2015, 521, 208-212. [CrossRef] [PubMed]
• Jansson, J.K.; Tas, N. The microbial ecology of permafrost. Nat. Rev. Microbiol. 2014, 12, 414-425. [CrossRef] [PubMed]
• Price, P.B. A habitat for psychrophiles in deep Antarctic ice. Proc. Natl. Acad. Sci. USA 2000, 97, 1247-1251. [CrossRef] [PubMed]
• Price, P.B. Microbial life in glacial ice and implications for a cold origin of life. FEMS Microbiol. Ecol. 2007, 59, 217-231. [CrossRef] [PubMed]
• Price, P.B.; Sowers, T. Temperature dependence of metabolic rates for microbial growth, maintenance, and survival. Proc. Natl. Acad. Sci. USA 2004, 101, 4631-4636. [CrossRef] [PubMed]
• Rohde, R.A.; Price, P.B. Diffusion-controlled metabolism for long-term survival of single isolated microorganisms trapped within ice crystals. Proc. Natl. Acad. Sci. USA 2007, 104, 16592-16597. [CrossRef] [PubMed]
• Rohde, R.A.; Price, P.B.; Bay, R.C.; Bramall, N.E. In situ microbial metabolism as a cause of gas anomalies in ice. Proc. Natl. Acad. Sci. USA 2008, 105, 8667-8672. [CrossRef] [PubMed]
• Price, P.B. Microbial genesis, life and death in glacial ice. Can. J. Microbiol. 2009, 55, 1-11. [CrossRef] [PubMed]
• Tung, H.C.; Bramall, N.E.; Price, P.B. Microbial origin of excess methane in glacial ice and implications for life on Mars. Proc. Natl. Acad. Sci. USA 2005, 102, 18292-18296. [CrossRef] [PubMed]
• Piette, F.; D’Amico, S.; Struvay, C.; Mazzucchelli, G.; Renaut, J.; Tutino, M.L.; Danchin, A.; Leprince, P.; Feller, G. Proteomics of life at low temperatures: Trigger factor is the primary chaperone in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125. Mol. Microbiol. 2010, 76, 120-132. [CrossRef] [PubMed]
• Thomas, D.N.; Dieckmann, G.S. Antarctic Sea ice-a habitat for extremophiles. Science 2002, 295, 641-644. [CrossRef] [PubMed]
• Clarke, A.; Morris, G.J.; Fonseca, F.; Murray, B.J.; Acton, E.; Price, H.C. A low temperature limit for life on Earth. PLoS ONE 2013, 8, e66207. [CrossRef] [PubMed]
• Bidle, K.D.; Lee, S.; Marchant, D.R.; Falkowski, P.G. Fossil genes and microbes in the oldest ice on Earth. Proc. Natl. Acad. Sci. USA 2007, 104, 13455-13460. [CrossRef] [PubMed]
• Menor-Salvan, C.; Marin-Yaseli, M.R. Prebiotic chemistry in eutectic solutions at the water-ice matrix. Chem. Soc. Rev. 2012, 41, 5404-5415. [CrossRef] [PubMed]
• Trinks, H.; Schroder, W.; Biebricher, C.K. Ice and the origin of life. Orig. Life Evol. Biosph. 2005, 35, 429-445. [CrossRef] [PubMed]
• Attwater, J.; Wochner, A.; Pinheiro, V.B.; Coulson, A.; Holliger, P. Ice as a protocellular medium for RNA replication. Nat. Commun. 2010, 1, 76. [CrossRef] [PubMed]
• Attwater, J.; Wochner, A.; Holliger, P. In-ice evolution of RNA polymerase ribozyme activity. Nat. Chem.2013, 5, 1011-1018. [CrossRef] [PubMed]
• Mutschler, H.; Wochner, A.; Holliger, P. Freeze-thaw cycles as drivers of complex ribozyme assembly. Nat. Chem. 2015, 7, 502-508. [CrossRef] [PubMed]
• Kasting, J.F.; Catling, D. Evolution of a habitable planet. Annu. Rev. Astron. Astrophys. 2003, 41, 429-463. [CrossRef]