An extremophile (from Latin extremus meaning "extreme" and Greek philiā (φιλία) meaning "love") is an organism with optimal growth in environmental conditions considered extreme in comparison to the environmental conditions that are comfortable to humans. In contrast, organisms that live in more moderate environmental conditions, according to an anthropocentric view, may be termed mesophiles or neutrophiles.
In the 1980s and 1990s, biologists found that microbial life has great flexibility for surviving in extreme environments—niches that are acidic or extraordinarily hot, for example—that would be completely inhospitable to complex organisms. Some scientists even concluded that life may have begun on Earth in hydrothermal vents far under the ocean's surface.
According to astrophysicist Steinn Sigurdsson, "There are viable bacterial spores that have been found that are 40 million years old on Earth—and we know they're very hardened to radiation." Some bacteria were found living in the cold and dark in a lake buried a half-mile deep under the ice in Antarctica, and in the Marianas Trench, the deepest place in Earth's oceans. Some microorganisms have been found thriving inside rocks up to 1,900 feet (580 m) below the sea floor under 8,500 feet (2,600 m) of ocean off the coast of the northwestern United States. According to one of the researchers, "You can find microbes everywhere—they're extremely adaptable to conditions, and survive wherever they are." A key to extremophile adaptation is their amino acid composition, affecting their protein folding ability under particular conditions.
Tom Gheysens from Ghent University in Belgium and some of his colleagues have presented research findings that show spores from a species of Bacillus bacteria survived and were still viable after being heated to temperatures of 420 °C (788 °F).
|The limits of known life on Earth.|
|Factor||Environment / source||Limits||Examples|
|High temperature||Submarine hydrothermal vents||110 °C to 121 °C||Pyrolobus fumarii, Pyrococcus furiosus|
|Low temperature||Ice||-17 °C to -20 °C||Synechococcus lividus|
|Alkaline systems||Soda lakes||pH > 11||Psychrobacter, Vibrio, Arthrobacter, Natronobacterium|
|Acidic systems||Volcanic springs, acid mine drainage||pH -0.06 to 1.0||Bacillus, Clostridium paradoxum|
|Ionizing radiation||Cosmic rays, X-rays, radioactive decay||1,500 to 6,000 Gy||Deinococcus radiodurans, Rubrobacter, Thermococcus gammatolerans|
|UV radiation||Sunlight||5,000 J/m2||Deinococcus radiodurans, Rubrobacter, Thermococcus gammatolerans|
|High pressure||Mariana Trench||1,100 bar||Pyrococcus sp.|
|Salinity||High salt concentration||aw ~ 0.6||Halobacteriaceae, Dunaliella salina|
|Desiccation||Atacama Desert (Chile), McMurdo Dry Valleys (Antarctica)||~60% relative humidity||Chroococcidiopsis|
|Deep crust||accessed at some gold mines||Halicephalobus mephisto, Mylonchulus brachyurus, unidentified arthropods|
There are many classes of extremophiles that range all around the globe; each corresponding to the way its environmental niche differs from mesophilic conditions. These classifications are not exclusive. Many extremophiles fall under multiple categories and are classified as polyextremophiles. For example, organisms living inside hot rocks deep under Earth's surface are thermophilic and barophilic such as Thermococcus barophilus. A polyextremophile living at the summit of a mountain in the Atacama Desert might be a radioresistant xerophile, a psychrophile, and an oligotroph. Polyextremophiles are well known for their ability to tolerate both high and low pH levels.
- An organism with optimal growth at pH levels of 3.0 or below
- An organism with optimal growth at pH levels of 9.0 or above
- An organism with optimal growth in the absence of molecular oxygen. Two sub-types exist: facultative anaerobe and obligate anaerobe. A facultative anaerobe can tolerate anoxic and oxic conditions; however, an obligate anaerobe dies in the presence of even trace levels of molecular oxygen.
- An organism that lives in microscopic spaces within rocks, such as pores between aggregate grains. These may also be called endolith, a term that also includes organisms populating fissures, aquifers, and faults filled with groundwater in the deep subsurface.
- An organism with optimal growth at a concentration of dissolved salts of 50 g/L (= 5% m/v) or above.
- An organism with optimal growth at hydrostatic pressures above 50 MPa (= 493 atm = 7,252 psi).
- An organism with optimal growth at temperatures above 80 °C (176 °F).
- An organism that lives underneath rocks in cold deserts.
- Capable of tolerating high levels of dissolved heavy metals in solution, such as copper, cadmium, arsenic, and zinc. Examples include Ferroplasma sp., Cupriavidus metallidurans and GFAJ-1.
- An organism with optimal growth in nutritionally limited environments.
- An organism with optimal growth in environments with a high sugar concentration.
- An organism with optimal growth in hydrostatic pressures above 10 MPa (= 99 atm = 1,450 psi). Also referred to as barophile.
- A polyextremophile (faux Ancient Latin/Greek for 'affection for many extremes') is an organism that qualifies as an extremophile under more than one category.
- An organism with optimal growth at temperatures of 15 °C (59 °F) or lower.
- Organisms resistant to high levels of ionizing radiation, most commonly ultraviolet radiation. This category also includes organisms capable of resisting nuclear radiation.
- An organism with optimal growth at temperatures above 45 °C (113 °F).
- An organism with optimal growth at water activity below 0.8.
Astrobiology is the study of the origin, evolution, distribution, and future of life in the universe: extraterrestrial life and life on Earth. Astrobiology makes use of physics, chemistry, astronomy, solar physics, biology, molecular biology, ecology, planetary science, geography, and geology to investigate the possibility of life on other worlds and help recognize biospheres that might be different from that on Earth. Astrobiologists are particularly interested in studying extremophiles, as their habitats may be analogous to conditions on other planets. For example, analogous deserts of Antarctica are exposed to harmful UV radiation, low temperature, high salt concentration and low mineral concentration. These conditions are similar to those on Mars. Therefore, finding viable microbes in the subsurface of Antarctica suggests that there may be microbes surviving in endolithic communities and living under the Martian surface. Research indicates it is unlikely that Martian microbes exist on the surface or at shallow depths, but may be found at subsurface depths of around 100 meters.
Recent research carried out on extremophiles in Japan involved a variety of bacteria including Escherichia coli and Paracoccus denitrificans being subject to conditions of extreme gravity. The bacteria were cultivated while being rotated in an ultracentrifuge at high speeds corresponding to 403,627 g (i.e. 403,627 times the gravity experienced on Earth). Paracoccus denitrificans was one of the bacteria which displayed not only survival but also robust cellular growth under these conditions of hyperacceleration which are usually found only in cosmic environments, such as on very massive stars or in the shock waves of supernovas. Analysis showed that the small size of prokaryotic cells is essential for successful growth under hypergravity. The research has implications on the feasibility of panspermia.
On 26 April 2012, scientists reported that lichen survived and showed remarkable results on the adaptation capacity of photosynthetic activity within the simulation time of 34 days under Martian conditions in the Mars Simulation Laboratory (MSL) maintained by the German Aerospace Center (DLR).
On 29 April 2013, scientists at Rensselaer Polytechnic Institute, funded by NASA, reported that, during spaceflight on the International Space Station, microbes seem to adapt to the space environment in ways "not observed on Earth" and in ways that "can lead to increases in growth and virulence".
On 19 May 2014, scientists announced that numerous microbes, like Tersicoccus phoenicis, may be resistant to methods usually used in spacecraft assembly clean rooms. It's not currently known if such resistant microbes could have withstood space travel and are present on the Curiosity rover now on the planet Mars.
On 20 August 2014, scientists confirmed the existence of microorganisms living half a mile below the ice of Antarctica.
On September 2015, scientists from CNR-National Research Council of Italy reported that S.soflataricus was able to survive under Martian radiation at a wavelength that was considered extremely lethal to most bacteria. This discovery is significant because it indicates that not only bacterial spores, but also growing cells can be remarkably resistant to strong UV radiation.
On June 2016, scientists from Brigham Young University conclusively reported that endospores of Bacillus subtilis were able to survive high speed impacts up to 299±28 m/s, extreme shock, and extreme deceleration. They pointed out that this feature might allow endospores to survive and to be transferred between planets by traveling within meteorites or by experiencing atmosphere disruption. Moreover, they suggested that the landing of spacecraft may also result in interplanetary spore transfer, given that spores can survive high-velocity impact while ejected from the spacecraft onto the planet surface. This is the first study which reported that bacteria can survive in such high-velocity impact. However, the lethal impact speed is unknown, and further experiments should be done by introducing higher-velocity impact to bacterial endospores.
Examples and recent findings
New sub-types of -philes are identified frequently and the sub-category list for extremophiles is always growing. For example, microbial life lives in the liquid asphalt lake, Pitch Lake. Research indicates that extremophiles inhabit the asphalt lake in populations ranging between 106 to 107 cells/gram. Likewise, until recently boron tolerance was unknown but a strong borophile was discovered in bacteria. With the recent isolation of Bacillus boroniphilus, borophiles came into discussion. Studying these borophiles may help illuminate the mechanisms of both boron toxicity and boron deficiency.
In July 2019, a scientific study of Kidd Mine in Canada discovered sulfur-breathing organisms which live 7900 feet below the surface, and which breathe sulfur in order to survive. These organisms are also remarkable due to eating rocks such as pyrite as their regular food source.
The thermoalkaliphilic catalase, which initiates the breakdown of hydrogen peroxide into oxygen and water, was isolated from an organism, Thermus brockianus, found in Yellowstone National Park by Idaho National Laboratory researchers. The catalase operates over a temperature range from 30 °C to over 94 °C and a pH range from 6–10. This catalase is extremely stable compared to other catalases at high temperatures and pH. In a comparative study, the T. brockianus catalase exhibited a half life of 15 days at 80 °C and pH 10 while a catalase derived from Aspergillus niger had a half life of 15 seconds under the same conditions. The catalase will have applications for removal of hydrogen peroxide in industrial processes such as pulp and paper bleaching, textile bleaching, food pasteurization, and surface decontamination of food packaging.
DNA modifying enzymes such as Taq DNA polymerase and some Bacillus enzymes used in clinical diagnostics and starch liquefaction are produced commercially by several biotechnology companies.
Over 65 prokaryotic species are known to be naturally competent for genetic transformation, the ability to transfer DNA from one cell to another cell followed by integration of the donor DNA into the recipient cell's chromosome. Several extremophiles are able to carry out species-specific DNA transfer, as described below. However, it is not yet clear how common such a capability is among extremophiles.
The bacterium Deinococcus radiodurans is one of the most radioresistant organisms known. This bacterium can also survive cold, dehydration, vacuum and acid and is thus known as a polyextremophile. D. radiodurans is competent to perform genetic transformation. Recipient cells are able to repair DNA damage in donor transforming DNA that had been UV irradiated as efficiently as they repair cellular DNA when the cells themselves are irradiated. The extreme thermophilic bacterium Thermus thermophilus and other related Thermus species are also capable of genetic transformation.
Halobacterium volcanii, an extreme halophilic (saline tolerant) archaeon, is capable of natural genetic transformation. Cytoplasmic bridges are formed between cells that appear to be used for DNA transfer from one cell to another in either direction.
Sulfolobus solfataricus and Sulfolobus acidocaldarius are hyperthermophilic archaea. Exposure of these organisms to the DNA damaging agents UV irradiation, bleomycin or mitomycin C induces species-specific cellular aggregation. UV-induced cellular aggregation of S. acidocaldarius mediates chromosomal marker exchange with high frequency. Recombination rates exceed those of uninduced cultures by up to three orders of magnitude. Frols et al. and Ajon et al. hypothesized that cellular aggregation enhances species-specific DNA transfer between Sulfolobus cells in order to repair damaged DNA by means of homologous recombination. Van Wolferen et al. noted that this DNA exchange process may be crucial under DNA damaging conditions such as high temperatures. It has also been suggested that DNA transfer in Sulfolobus may be an early form of sexual interaction similar to the more well-studied bacterial transformation systems that involve species-specific DNA transfer leading to homologous recombinational repair of DNA damage (and see Transformation (genetics)).
Extracellular membrane vesicles (MVs) might be involved in DNA transfer between different hyperthermophilic archaeal species. and viral genomes can be transferred via MVs. Notably, a horizontal plasmid transfer has been documented between hyperthermophilic Thermococcus and Methanocaldococcus species, respectively belonging to the orders Thermococcales and Methanococcales.It has been shown that both plasmids
- List of microorganisms tested in outer space
- RISE project
Specific types of organisms
- Dissimilatory metal-reducing microorganisms
- Canganella, Francesco; Wiegel, Juergen (April 2011). "Extremophiles: from abyssal to terrestrial ecosystems and possibly beyond". Naturwissenschaften. 98 (4): 253–279. doi:10.1007/s00114-011-0775-2. ISSN 0028-1042. PMID 21394529.
- Cavicchioli, Ricardo; Amils, Ricardo; Wagner, Dirk; McGenity, Terry (August 2011). "Life and applications of extremophiles: Editorial" (PDF). Environmental Microbiology. 13 (8): 1903–1907. doi:10.1111/j.1462-2920.2011.02512.x. PMID 22236328.
- Horikoshi, Koki; Bull, Alan T. (2011), Horikoshi, Koki (ed.), "Prologue: Definition, Categories, Distribution, Origin and Evolution, Pioneering Studies, and Emerging Fields of Extremophiles", Extremophiles Handbook, Springer Japan, pp. 3–15, doi:10.1007/978-4-431-53898-1_1, ISBN 9784431538981
- "Mars Exploration Rover Launches - Press kit" (PDF). NASA. June 2003. Retrieved 14 July 2009.
- BBC Staff (23 August 2011). "Impacts 'more likely' to have spread life from Earth". BBC. Retrieved 24 August 2011.
- Gorman J (6 February 2013). "Bacteria Found Deep Under Antarctic Ice, Scientists Say". The New York Times. Retrieved 6 February 2013.
- Choi CQ (17 March 2013). "Microbes Thrive in Deepest Spot on Earth". LiveScience. Retrieved 17 March 2013.
- Glud RN, Wenzhöfer F, Middelboe M, Oguri K, Turnewitsch R, Canfield DE, Kitazato H (17 March 2013). "High rates of microbial carbon turnover in sediments in the deepest oceanic trench on Earth". Nature Geoscience. 6 (4): 284–288. Bibcode:2013NatGe...6..284G. doi:10.1038/ngeo1773.
- Oskin B (14 March 2013). "Intraterrestrials: Life Thrives in Ocean Floor". LiveScience. Retrieved 17 March 2013.
- Reed CJ, Lewis H, Trejo E, Winston V, Evilia C (2013). "Protein adaptations in archaeal extremophiles". Archaea. 2013: 373275. doi:10.1155/2013/373275. PMC 3787623. PMID 24151449.
- "NASA Astrobiology Strategy" (PDF). NASA. 2015. p. 59. Archived from the original (PDF) on 22 December 2016. Retrieved 12 October 2017.
- Marteinsson VT, Birrien JL, Reysenbach AL, Vernet M, Marie D, Gambacorta A, Messner P, Sleytr UB, Prieur D (April 1999). "Thermococcus barophilus sp. nov., a new barophilic and hyperthermophilic archaeon isolated under high hydrostatic pressure from a deep-sea hydrothermal vent". International Journal of Systematic Bacteriology. 49 Pt 2 (2): 351–9. doi:10.1099/00207713-49-2-351. PMID 10319455.
- Yadav AN, Verma P, Kumar M, Pal KK, Dey R, Gupta A, et al. (31 May 2014). "Diversity and phylogenetic profiling of niche-specific Bacilli from extreme environments of India". Annals of Microbiology. 65 (2): 611–629. doi:10.1007/s13213-014-0897-91 (inactive 1 December 2019).
- "Studies refute arsenic bug claim". BBC News. 9 July 2012. Retrieved 10 July 2012.
- Erb TJ, Kiefer P, Hattendorf B, Günther D, Vorholt JA (July 2012). "GFAJ-1 is an arsenate-resistant, phosphate-dependent organism". Science. 337 (6093): 467–70. Bibcode:2012Sci...337..467E. doi:10.1126/science.1218455. PMID 22773139.
- Reaves ML, Sinha S, Rabinowitz JD, Kruglyak L, Redfield RJ (July 2012). "Absence of detectable arsenate in DNA from arsenate-grown GFAJ-1 cells". Science. 337 (6093): 470–3. arXiv:1201.6643. Bibcode:2012Sci...337..470R. doi:10.1126/science.1219861. PMC 3845625. PMID 22773140.
- Ward PD, Brownlee D (2004). The life and death of planet Earth. New York: Owl Books. ISBN 978-0-8050-7512-0.
- Chang K (12 September 2016). "Visions of Life on Mars in Earth's Depths". The New York Times. Retrieved 12 September 2016.
- Wynn-Williams DA, Newton EM, Edwards HG (2001). Exo-/astro-biology : proceedings of the first European workshop, 21 - 23 May 2001, ESRIN, Fracscati, Italy. Exo-/Astro-Biology. 496. p. 226. Bibcode:2001ESASP.496..225W. ISBN 978-92-9092-806-5.
- Than, Ker (25 April 2011). "Bacteria Grow Under 400,000 Times Earth's Gravity". National Geographic- Daily News. National Geographic Society. Retrieved 28 April 2011.
- Deguchi S, Shimoshige H, Tsudome M, Mukai SA, Corkery RW, Ito S, Horikoshi K (May 2011). "Microbial growth at hyperaccelerations up to 403,627 x g". Proceedings of the National Academy of Sciences of the United States of America. 108 (19): 7997–8002. Bibcode:2011PNAS..108.7997D. doi:10.1073/pnas.1018027108. PMC 3093466. PMID 21518884.
- Reuell, Peter (8 July 2019). "Harvard study suggests asteroids might play key role in spreading life". Harvard Gazette. Retrieved 6 October 2019.
- Baldwin E (26 April 2012). "Lichen survives harsh Mars environment". Skymania News. Retrieved 27 April 2012.
- De Vera JP, Kohler U (26 April 2012). "The adaptation potential of extremophiles to Martian surface conditions and its implication for the habitability of Mars" (PDF). Egu General Assembly Conference Abstracts. 14: 2113. Bibcode:2012EGUGA..14.2113D. Retrieved 27 April 2012.
- Kim W, Tengra FK, Young Z, Shong J, Marchand N, Chan HK, et al. (29 April 2013). "Spaceflight promotes biofilm formation by Pseudomonas aeruginosa". PLOS ONE. 8 (4): e62437. Bibcode:2013PLoSO...862437K. doi:10.1371/journal.pone.0062437. PMC 3639165. PMID 23658630.
- Madhusoodanan J (19 May 2014). "Microbial stowaways to Mars identified". Nature. doi:10.1038/nature.2014.15249. Retrieved 23 May 2014.
- Fox D (August 2014). "Lakes under the ice: Antarctica's secret garden". Nature. 512 (7514): 244–6. Bibcode:2014Natur.512..244F. doi:10.1038/512244a. PMID 25143097.
- Mack E (20 August 2014). "Life Confirmed Under Antarctic Ice; Is Space Next?". Forbes. Retrieved 21 August 2014.
- Mastascusa V, Romano I, Di Donato P, Poli A, Della Corte V, Rotundi A, Bussoletti E, Quarto M, Pugliese M, Nicolaus B (September 2014). "Extremophiles survival to simulated space conditions: an astrobiology model study". Origins of Life and Evolution of the Biosphere. 44 (3): 231–7. Bibcode:2014OLEB...44..231M. doi:10.1007/s11084-014-9397-y. PMC 4669584. PMID 25573749.
- Barney BL, Pratt SN, Austin DE (June 2016). "Survivability of bare, individual Bacillus subtilis spores to high-velocity surface impact: Implications for microbial transfer through space". Planetary and Space Science. 125: 20–26. Bibcode:2016P&SS..125...20B. doi:10.1016/j.pss.2016.02.010.
- Microbial Life Found in Hydrocarbon Lake. the physics arXiv blog 15 April 2010.
- Schulze-Makuch, Haque, Antonio, Ali, Hosein, Song, Yang, Zaikova, Beckles, Guinan, Lehto, Hallam. Microbial Life in a Liquid Asphalt Desert.
- Ahmed I, Yokota A, Fujiwara T (March 2007). "A novel highly boron tolerant bacterium, Bacillus boroniphilus sp. nov., isolated from soil, that requires boron for its growth". Extremophiles. 11 (2): 217–24. doi:10.1007/s00792-006-0027-0. PMID 17072687.
- ‘Follow the Water’: Hydrogeochemical Constraints on Microbial Investigations 2.4 km Below Surface at the Kidd Creek Deep Fluid and Deep Life Observatory, Garnet S. Lollar, Oliver Warr, Jon Telling, Magdalena R. Osburn & Barbara Sherwood Lollar, Received 15 Jan 2019, Accepted 01 Jul 2019, Published online: 18 Jul 2019.
- World’s Oldest Groundwater Supports Life Through Water-Rock Chemistry, July 29, 2019, deepcarbon.net.
- Strange life-forms found deep in a mine point to vast 'underground Galapagos', By Corey S. Powell, Sept. 7, 2019, nbcnews.com.
- "Bioenergy and Industrial Microbiology". Idaho National Laboratory. U.S. Department of Energy. Retrieved 3 February 2014.
- Anitori RP, ed. (2012). Extremophiles: Microbiology and Biotechnology. Caister Academic Press. ISBN 978-1-904455-98-1.
- Johnsborg O, Eldholm V, Håvarstein LS (December 2007). "Natural genetic transformation: prevalence, mechanisms and function". Research in Microbiology. 158 (10): 767–78. doi:10.1016/j.resmic.2007.09.004. PMID 17997281.
- Moseley BE, Setlow JK (September 1968). "Transformation in Micrococcus radiodurans and the ultraviolet sensitivity of its transforming DNA". Proceedings of the National Academy of Sciences of the United States of America. 61 (1): 176–83. Bibcode:1968PNAS...61..176M. doi:10.1073/pnas.61.1.176. PMC 285920. PMID 5303325.
- Koyama Y, Hoshino T, Tomizuka N, Furukawa K (April 1986). "Genetic transformation of the extreme thermophile Thermus thermophilus and of other Thermus spp". Journal of Bacteriology. 166 (1): 338–40. doi:10.1128/jb.166.1.338-340.1986. PMC 214599. PMID 3957870.
- Rosenshine I, Tchelet R, Mevarech M (September 1989). "The mechanism of DNA transfer in the mating system of an archaebacterium". Science. 245 (4924): 1387–9. Bibcode:1989Sci...245.1387R. doi:10.1126/science.2818746. PMID 2818746.
- Fröls S, Ajon M, Wagner M, Teichmann D, Zolghadr B, Folea M, Boekema EJ, Driessen AJ, Schleper C, Albers SV, et al. (November 2008). "UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation". Molecular Microbiology. 70 (4): 938–52. doi:10.1111/j.1365-2958.2008.06459.x. PMID 18990182.
- Ajon M, Fröls S, van Wolferen M, Stoecker K, Teichmann D, Driessen AJ, Grogan DW, Albers SV, Schleper C, et al. (November 2011). "UV-inducible DNA exchange in hyperthermophilic archaea mediated by type IV pili" (PDF). Molecular Microbiology. 82 (4): 807–17. doi:10.1111/j.1365-2958.2011.07861.x. PMID 21999488.
- van Wolferen M, Ajon M, Driessen AJ, Albers SV (July 2013). "How hyperthermophiles adapt to change their lives: DNA exchange in extreme conditions". Extremophiles. 17 (4): 545–63. doi:10.1007/s00792-013-0552-6. PMID 23712907.
- Gaudin M, Gauliard E, Schouten S, Houel-Renault L, Lenormand P, Marguet E, Forterre P (February 2013). "Hyperthermophilic archaea produce membrane vesicles that can transfer DNA". Environmental Microbiology Reports. 5 (1): 109–16. doi:10.1111/j.1758-2229.2012.00348.x. PMID 23757139.
- Krupovic M, Gonnet M, Hania WB, Forterre P, Erauso G (2013). "Insights into dynamics of mobile genetic elements in hyperthermophilic environments from five new Thermococcus plasmids". PLOS ONE. 8 (1): e49044. Bibcode:2013PLoSO...849044K. doi:10.1371/journal.pone.0049044. PMC 3543421. PMID 23326305.
- Wilson ZE, Brimble MA (January 2009). "Molecules derived from the extremes of life". Natural Product Reports. 26 (1): 44–71. doi:10.1039/b800164m. PMID 19374122.
- Rossi M, Ciaramella M, Cannio R, Pisani FM, Moracci M, Bartolucci S (July 2003). "Extremophiles 2002". Journal of Bacteriology. 185 (13): 3683–9. doi:10.1128/JB.185.13.3683-3689.2003. PMC 161588. PMID 12813059.
- C.Michael Hogan (2010). "Extremophile". Encyclopedia of Earth, National Council of Science & the Environment, Eds. E. Monosson & C. Cleveland.
- Seckbach J, Oren A, Stan-Lotter H, eds. (2013). Polyextremophiles: life under multiple forms of stress. Dordrecht: Springer. ISBN 978-94-007-6488-0.
|Wikinews has related news: Bacteria thrive deep under sea floor|
- Extreme Environments - Science Education Resource Center
- Extremophile Research
- Eukaryotes in extreme environments
- The Research Center of Extremophiles
- DaveDarling's Encyclopedia of Astrobiology, Astronomy, and Spaceflight
- The International Society for Extremophiles
- Idaho National Laboratory
- Polyextremophile on David Darling's Encyclopedia of Astrobiology, Astronomy, and Spaceflight
- T-Limit Expedition