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Hypothetical types of biochemistry

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False-color Cassini radar mosaic of Titan's north polar region; the blue areas are lakes of liquid hydrocarbons.
"The existence of lakes of liquid hydrocarbons on Titan opens up the possibility for solvents and energy sources that are alternatives to those in our biosphere and that might support novel life forms altogether different from those on Earth."—NASA Astrobiology Roadmap 2008[1]

Several forms of biochemistry are agreed to be scientifically viable but are not proven to exist at this time.[2] The kinds of living organisms currently known on Earth all use carbon compounds for basic structural and metabolic functions, water as a solvent, and DNA or RNA to define and control their form. If life exists on other planets or moons it may be chemically similar, though it is also possible that there are organisms with quite different chemistries[3] – for instance, involving other classes of carbon compounds, compounds of another element, or another solvent in place of water.

The possibility of life-forms being based on "alternative" biochemistries is the topic of an ongoing scientific discussion, informed by what is known about extraterrestrial environments and about the chemical behaviour of various elements and compounds. It is of interest in synthetic biology and is also a common subject in science fiction.

The element silicon has been much discussed as a hypothetical alternative to carbon. Silicon is in the same group as carbon on the periodic table and, like carbon, it is tetravalent. Hypothetical alternatives to water include ammonia, which, like water, is a polar molecule, and cosmically abundant; and non-polar hydrocarbon solvents such as methane and ethane, which are known to exist in liquid form on the surface of Titan.

Overview of hypothetical types of biochemistry

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Overview of hypothetical types of biochemistry
Type Basis Brief description Remarks
Alternative-chirality biomolecules Alternative biochemistry Mirror image biochemistry Perhaps the least unusual alternative biochemistry would be one with differing chirality of its biomolecules. In known Earth-based life, amino acids are almost universally of the L form and sugars are of the D form. Molecules using D amino acids or L sugars are possible, though they would be incompatible with organisms using the opposing chirality molecules. Gram-positive bacteria incorporate D-alanine into their peptidoglycan layer, created through the actions of racemases.[4]
Ammonia biochemistry Non-water solvents Ammonia-based life Ammonia is relatively abundant in the universe and has chemical similarities to water. The possible role of liquid ammonia as an alternative solvent for life is an idea that goes back at least to 1954, when J. B. S. Haldane raised the topic at a symposium about life's origin.[citation needed]
Arsenic biochemistry Alternative biochemistry Arsenic-based life Arsenic, which is chemically similar to phosphorus, while poisonous for most life forms on Earth, is incorporated into the biochemistry of some organisms.[citation needed]
Borane biochemistry (Organoboron chemistry) Alternative biochemistry Boranes-based life Boranes are dangerously explosive in Earth's atmosphere, but would be more stable in a reducing environment (an atmosphere without oxygen or other oxidizing gases, and which may contain actively reductant gases such as hydrogen, carbon monoxide, methane and hydrogen sulfide). Boron, however, is exceedingly rare in the universe in comparison to its neighbours carbon, nitrogen, and oxygen. On the other hand, structures containing alternating boron and nitrogen atoms share some properties with hydrocarbons.[citation needed]
Cosmic necklace-based biology Nonplanetary life Non-chemical life In 2020, Luis A. Anchordoqu and Eugene M. Chudnovsky hypothesized that life composed of magnetic semipoles connected by cosmic strings could evolve inside stars.[5]
Dusty plasma-based biology Nonplanetary life Non-chemical life In 2007, Vadim N. Tsytovich and colleagues proposed that lifelike behaviors could be exhibited by dust particles suspended in a plasma, under conditions that might exist in space.[6]
Extremophiles Alternative environment Life in variable environments It would be biochemically possible to sustain life in environments that are only periodically consistent with life as we know it, such as extremely high or low temperatures, pressures, or pH; or the present of high levels of salt or nuclear radiation.[citation needed]
Heteropoly acid biochemistry Alternative biochemistry Heteropoly acid-based life Various metals can form complex structures with oxygen, such as heteropoly acids.[citation needed]
Hydrogen fluoride biochemistry Non-water solvents Hydrogen fluoride-based life Hydrogen fluoride has been considered as a possible solvent for life by scientists such as Peter Sneath.[citation needed]
Hydrogen sulfide biochemistry Non-water solvents Hydrogen sulfide-based life Hydrogen sulfide is a chemical analog of water, but is less polar and a weaker inorganic solvent.[citation needed]
Methane biochemistry (Azotosome) Non-water solvents Methane-based life Methane (CH4) is relatively abundant in the solar system and the universe, and is known to exist in liquid form on Titan, the largest moon of Saturn. Though highly unlikely, it is considered to be possible for Titan to harbor life. If so, it will most likely be methane-based life.[citation needed]
Non-green photosynthesizers Other speculations Alternate plant life Physicists have noted that, although photosynthesis on Earth generally involves green plants, a variety of other-colored plants could also support photosynthesis, essential for most life on Earth, and that other colors might be preferred in places that receive a different mix of stellar radiation than Earth. In particular, retinal is capable of, and has been observed to, perform photosynthesis.[7] Bacteria capable of photosynthesis are known as microbial rhodopsins. A plant or creature that uses retinal photosynthesis is always purple.
Shadow biosphere Alternative environment A hidden life biosphere on Earth A shadow biosphere is a hypothetical microbial biosphere of Earth that uses radically different biochemical and molecular processes than currently known life. It could exist, for example, deep in the crust or sealed in ancient rocks.[citation needed]
Silicon biochemistry (Organosilicon) Alternative biochemistry Silicon-based life Like carbon, silicon can create molecules that are sufficiently large to carry biological information; however, the scope of possible silicon chemistry is far more limited than that of carbon.[citation needed]
Silicon dioxide biochemistry Non-water solvents Silicon dioxide-based life Gerald Feinberg and Robert Shapiro have suggested that molten silicate rock could serve as a liquid medium for organisms with a chemistry based on silicon, oxygen, and other elements such as aluminium.[citation needed]
Sulfur biochemistry Alternative biochemistry Sulfur-based life The biological use of sulfur as an alternative to carbon is purely hypothetical, especially because sulfur usually forms only linear chains rather than branched ones.[citation needed]
Alternative nucleic acids Alternative biochemistry Different genetic storage Xeno nucleic acids (XNA) may possibly be used in place of RNA or DNA. XNA is the general term for a nucleic acid with an altered sugar backbone. Examples of XNA are TNA, which uses threose, HNA, which uses 1,5-anhydrohexitol, GNA, which uses glycol, CeNA, which uses cyclohexene, LNA, which utilizes a form of ribose that contains an extra linkage between its 4' carbon and 2' oxygen, FANA, which uses arabinose but with a single fluorine atom attached to its 2' carbon, and PNA, which uses, in place of sugar and phosphate, N-(2-aminoethyl)-glycine units connected by peptide bonds.[8] In comparison, Hachimoji DNA changes the base pairs instead of the backbone. These new base pairs are P (2-Aminoimidazo[1,2a][1,3,5]triazin-4(1H)-one), Z (6-Amino-5-nitropyridin-2-one), B (Isoguanine), and S (rS = Isocytosine for RNA, dS = 1-Methylcytosine for DNA).[9][10]

Shadow biosphere

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Main article: Shadow biosphere
The Arecibo message (1974) sent information into space about basic chemistry of Earth life.

A shadow biosphere is a hypothetical microbial biosphere of Earth that uses radically different biochemical and molecular processes than currently known life.[11][12] Although life on Earth is relatively well-studied, the shadow biosphere may still remain unnoticed because the exploration of the microbial world targets primarily the biochemistry of the macro-organisms.

Alternative-chirality biomolecules

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Perhaps the least unusual alternative biochemistry would be one with differing chirality of its biomolecules. In known Earth-based life, amino acids are almost universally of the L form and sugars are of the D form. Molecules using D amino acids or L sugars may be possible; molecules of such a chirality, however, would be incompatible with organisms using the opposing chirality molecules. Amino acids whose chirality is opposite to the norm are found on Earth, and these substances are generally thought to result from decay of organisms of normal chirality. However, physicist Paul Davies speculates that some of them might be products of "anti-chiral" life.[13]

It is questionable, however, whether such a biochemistry would be truly alien. Although it would certainly be an alternative stereochemistry, molecules that are overwhelmingly found in one enantiomer throughout the vast majority of organisms can nonetheless often be found in another enantiomer in different (often basal) organisms such as in comparisons between members of Archaea and other domains,[citation needed] making it an open topic whether an alternative stereochemistry is truly novel.

Non-carbon-based biochemistries

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On Earth, all known living things have a carbon-based structure and system. Scientists have speculated about the pros and cons of using elements other than carbon to form the molecular structures necessary for life, but no one has proposed a theory employing such atoms to form all the necessary structures. However, as Carl Sagan argued, it is very difficult to be certain whether a statement that applies to all life on Earth will turn out to apply to all life throughout the universe.[14] Sagan used the term "carbon chauvinism" for such an assumption.[15] He regarded silicon and germanium as conceivable alternatives to carbon[15] (other plausible elements include but are not limited to palladium and titanium); but, on the other hand, he noted that carbon does seem more chemically versatile and is more abundant in the cosmos.[16] Norman Horowitz devised the experiments to determine whether life might exist on Mars that were carried out by the Viking Lander of 1976, the first U.S. mission to successfully land a probe on the surface of Mars. Horowitz argued that the great versatility of the carbon atom makes it the element most likely to provide solutions, even exotic solutions, to the problems of survival on other planets.[17] He considered that there was only a remote possibility that non-carbon life forms could exist with genetic information systems capable of self-replication and the ability to evolve and adapt.

Silicon biochemistry

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See also: Organosilicon
Structure of silane, analog of methane
Structure of the silicone polydimethylsiloxane (PDMS)
Marine diatoms – carbon-based organisms that extract silicon from sea water, in the form of its oxide (silica) and incorporate it into their cell walls

The silicon atom has been much discussed as the basis for an alternative biochemical system, because silicon has many chemical similarities to carbon and is in the same group of the periodic table. Like carbon, silicon can create molecules that are sufficiently large to carry biological information.[18]

However, silicon has several drawbacks as a carbon alternative. Carbon is ten times more cosmically abundant than silicon, and its chemistry appears naturally more complex.[19] By 1998, astronomers had identified 84 carbon-containing molecules in the interstellar medium, but only 8 containing silicon, of which half also included carbon.[20] Even though Earth and other terrestrial planets are exceptionally silicon-rich and carbon-poor (silicon is roughly 925 times more abundant in Earth's crust than carbon), terrestrial life bases itself on carbon. It may eschew silicon because silicon compounds are less varied, unstable in the presence of water, or block the flow of heat.[19]

Relative to carbon, silicon has a much larger atomic radius, and forms much weaker covalent bonds to atoms — except oxygen and fluorine, with which it forms very strong bonds.[18] Almost no multiple bonds to silicon are stable, although silicon does exhibit varied coordination number.[21] Silanes, silicon analogues to the alkanes, react rapidly with water, and long-chain silanes spontaneously decompose.[22] Consequently, most terrestrial silicon is "locked up" in silica, and not a wide variety of biogenic precursors.[21]

Silicones, which alternate between silicon and oxygen atoms, are much more stable than silanes, and may even be more stable than the equivalent hydrocarbons in sulfuric acid-rich extraterrestrial environments.[22] Alternatively, the weak bonds in silicon compounds may help maintain a rapid pace of life at cryogenic temperatures. Polysilanols, the silicon homologues to sugars, are among the few compounds soluble in liquid nitrogen.[23][unreliable source?][21]

All known silicon macromolecules are artificial polymers, and so "monotonous compared with the combinatorial universe of organic macromolecules".[18][21] Even so, some Earth life uses biogenic silica: diatoms' silicate skeletons. A. G. Cairns-Smith hypothesized that silicate minerals in water played a crucial role in abiogenesis, in that biogenic carbon compounds formed around their crystal structures.[24][25] Although not observed in nature, carbon–silicon bonds have been added to biochemistry under directed evolution (artificial selection): a cytochrome c protein from Rhodothermus marinus has been engineered to catalyze new carbon–silicon bonds between hydrosilanes and diazo compounds.[26]

Other exotic element-based biochemistries

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See also: Organoboron chemistry
  • Boranes are dangerously explosive in Earth's atmosphere, but would be more stable in a reducing atmosphere. However, boron's low cosmic abundance makes it less likely as a base for life than carbon.
  • Various metals, together with oxygen, can form very complex and thermally stable structures rivaling those of organic compounds;[citation needed] the heteropoly acids are one such family. Some metal oxides are also similar to carbon in their ability to form both nanotube structures and diamond-like crystals (such as cubic zirconia). Titanium, aluminium, magnesium, and iron are all more abundant in the Earth's crust than carbon. Metal-oxide-based life could therefore be a possibility under certain conditions, including those (such as high temperatures) at which carbon-based life would be unlikely. The Cronin group at Glasgow University reported self-assembly of tungsten polyoxometalates into cell-like spheres.[27] By modifying their metal oxide content, the spheres can acquire holes that act as porous membrane, selectively allowing chemicals in and out of the sphere according to size.[27]
  • Sulfur is also able to form long-chain molecules, but suffers from the same high-reactivity problems as phosphorus and silanes. The biological use of sulfur as an alternative to carbon is purely hypothetical, especially because sulfur usually forms only linear chains rather than branched ones. (The biological use of sulfur as an electron acceptor is widespread and can be traced back 3.5 billion years on Earth, thus predating the use of molecular oxygen.[28] Sulfur-reducing bacteria can utilize elemental sulfur instead of oxygen, reducing sulfur to hydrogen sulfide.)

Arsenic as an alternative to phosphorus

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See also: GFAJ-1

Arsenic, which is chemically similar to phosphorus, while poisonous for most life forms on Earth, is incorporated into the biochemistry of some organisms.[29] Some marine algae incorporate arsenic into complex organic molecules such as arsenosugars and arsenobetaines. Fungi and bacteria can produce volatile methylated arsenic compounds. Arsenate reduction and arsenite oxidation have been observed in microbes (Chrysiogenes arsenatis).[30] Additionally, some prokaryotes can use arsenate as a terminal electron acceptor during anaerobic growth and some can utilize arsenite as an electron donor to generate energy.

It has been speculated that the earliest life forms on Earth may have used arsenic biochemistry in place of phosphorus in the structure of their DNA.[31] A common objection to this scenario is that arsenate esters are so much less stable to hydrolysis than corresponding phosphate esters that arsenic is poorly suited for this function.[32]

The authors of a 2010 geomicrobiology study, supported in part by NASA, have postulated that a bacterium, named GFAJ-1, collected in the sediments of Mono Lake in eastern California, can employ such 'arsenic DNA' when cultured without phosphorus.[33][34] They proposed that the bacterium may employ high levels of poly-β-hydroxybutyrate or other means to reduce the effective concentration of water and stabilize its arsenate esters.[34] This claim was heavily criticized almost immediately after publication for the perceived lack of appropriate controls.[35][36] Science writer Carl Zimmer contacted several scientists for an assessment: "I reached out to a dozen experts ... Almost unanimously, they think the NASA scientists have failed to make their case".[37] Other authors were unable to reproduce their results and showed that the study had issues with phosphate contamination, suggesting that the low amounts present could sustain extremophile lifeforms.[38] Alternatively, it was suggested that GFAJ-1 cells grow by recycling phosphate from degraded ribosomes, rather than by replacing it with arsenate.[39]

Non-water solvents

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In addition to carbon compounds, all currently known terrestrial life also requires water as a solvent. This has led to discussions about whether water is the only liquid capable of filling that role. The idea that an extraterrestrial life-form might be based on a solvent other than water has been taken seriously in recent scientific literature by the biochemist Steven Benner,[40] and by the astrobiological committee chaired by John A. Baross.[41] Solvents discussed by the Baross committee include ammonia,[42] sulfuric acid,[43] formamide,[44] hydrocarbons,[44] and (at temperatures much lower than Earth's) liquid nitrogen, or hydrogen in the form of a supercritical fluid.[45]

Water as a solvent limits the forms biochemistry can take. For example, Steven Benner, proposes the polyelectrolyte theory of the gene that claims that for a genetic biopolymer such as, DNA, to function in water, it requires repeated ionic charges.[46] If water is not required for life, these limits on genetic biopolymers are removed.

Carl Sagan once described himself as both a carbon chauvinist and a water chauvinist;[47] however, on another occasion he said that he was a carbon chauvinist but "not that much of a water chauvinist".[48] He speculated on hydrocarbons,[48]: 11  hydrofluoric acid,[49] and ammonia[48][49] as possible alternatives to water.

Some of the properties of water that are important for life processes include:

  • A complexity which leads to a large number of permutations of possible reaction paths including acid–base chemistry, H+ cations, OH− anions, hydrogen bonding, van der Waals bonding, dipole–dipole and other polar interactions, aqueous solvent cages, and hydrolysis. This complexity offers a large number of pathways for evolution to produce life, many other solvents[which?] have dramatically fewer possible reactions, which severely limits evolution.
  • Thermodynamic stability: the free energy of formation of liquid water is low enough (−237.24 kJ/mol) that water undergoes few reactions. Other solvents are highly reactive, particularly with oxygen.
  • Water does not combust in oxygen because it is already the combustion product of hydrogen with oxygen. Most alternative solvents are not stable in an oxygen-rich atmosphere, so it is highly unlikely that those liquids could support aerobic life.
  • A large temperature range over which it is liquid.
  • High solubility of oxygen and carbon dioxide at room temperature supporting the evolution of aerobic aquatic plant and animal life.
  • A high heat capacity (leading to higher environmental temperature stability).
  • Water is a room-temperature liquid leading to a large population of quantum transition states required to overcome reaction barriers. Cryogenic liquids (such as liquid methane) have exponentially lower transition state populations which are needed for life based on chemical reactions. This leads to chemical reaction rates which may be so slow as to preclude the development of any life based on chemical reactions.[citation needed]
  • Spectroscopic transparency allowing solar radiation to penetrate several meters into the liquid (or solid), greatly aiding the evolution of aquatic life.
  • A large heat of vaporization leading to stable lakes and oceans.
  • The ability to dissolve a wide variety of compounds.
  • The solid (ice) has lower density than the liquid, so ice floats on the liquid. This is why bodies of water freeze over but do not freeze solid (from the bottom up). If ice were denser than liquid water (as is true for nearly all other compounds), then large bodies of liquid would slowly freeze solid, which would not be conducive to the formation of life.

Water as a compound is cosmically abundant, although much of it is in the form of vapor or ice. Subsurface liquid water is considered likely or possible on several of the outer moons: Enceladus (where geysers have been observed), Europa, Titan, and Ganymede. Earth and Titan are the only worlds currently known to have stable bodies of liquid on their surfaces.

Not all properties of water are necessarily advantageous for life, however.[50] For instance, water ice has a high albedo,[50] meaning that it reflects a significant quantity of light and heat from the Sun. During ice ages, as reflective ice builds up over the surface of the water, the effects of global cooling are increased.[50]

There are some properties that make certain compounds and elements much more favorable than others as solvents in a successful biosphere. The solvent must be able to exist in liquid equilibrium over a range of temperatures the planetary object would normally encounter. Because boiling points vary with the pressure, the question tends not to be does the prospective solvent remain liquid, but at what pressure. For example, hydrogen cyanide has a narrow liquid-phase temperature range at 1 atmosphere, but in an atmosphere with the pressure of Venus, with 92 bars (91 atm) of pressure, it can indeed exist in liquid form over a wide temperature range.

Ammonia

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The ammonia molecule (NH3), like the water molecule, is abundant in the universe, being a compound of hydrogen (the simplest and most common element) with another very common element, nitrogen.[51] The possible role of liquid ammonia as an alternative solvent for life is an idea that goes back at least to 1954, when J. B. S. Haldane raised the topic at a symposium about life's origin.[52]

Numerous chemical reactions are possible in an ammonia solution, and liquid ammonia has chemical similarities with water.[51][53] Ammonia can dissolve most organic molecules at least as well as water does and, in addition, it is capable of dissolving many elemental metals. Haldane made the point that various common water-related organic compounds have ammonia-related analogs; for instance the ammonia-related amine group (−NH2) is analogous to the water-related hydroxyl group (−OH).[53]

Ammonia, like water, can either accept or donate an H+ ion. When ammonia accepts an H+, it forms the ammonium cation (NH4+), analogous to hydronium (H3O+). When it donates an H+ ion, it forms the amide anion (NH2−), analogous to the hydroxide anion (OH−).[42] Compared to water, however, ammonia is more inclined to accept an H+ ion, and less inclined to donate one; it is a stronger nucleophile.[42] Ammonia added to water functions as Arrhenius base: it increases the concentration of the anion hydroxide. Conversely, using a solvent system definition of acidity and basicity, water added to liquid ammonia functions as an acid, because it increases the concentration of the cation ammonium.[53] The carbonyl group (C=O), which is much used in terrestrial biochemistry, would not be stable in ammonia solution, but the analogous imine group (C=NH) could be used instead.[42]

However, ammonia has some problems as a basis for life. The hydrogen bonds between ammonia molecules are weaker than those in water, causing ammonia's heat of vaporization to be half that of water, its surface tension to be a third, and reducing its ability to concentrate non-polar molecules through a hydrophobic effect. Gerald Feinberg and Robert Shapiro have questioned whether ammonia could hold prebiotic molecules together well enough to allow the emergence of a self-reproducing system.[54] Ammonia is also flammable in oxygen and could not exist sustainably in an environment suitable for aerobic metabolism.[55]

Titan's theorized internal structure, subsurface ocean shown in blue

A biosphere based on ammonia would likely exist at temperatures or air pressures that are extremely unusual in relation to life on Earth. Life on Earth usually exists between the melting point and boiling point of water, at a pressure designated as normal pressure, between 0 and 100 °C (273 and 373 K). When also held to normal pressure, ammonia's melting and boiling points are −78 °C (195 K) and −33 °C (240 K) respectively. Because chemical reactions generally proceed more slowly at lower temperatures, ammonia-based life existing in this set of conditions might metabolize more slowly and evolve more slowly than life on Earth.[55] On the other hand, lower temperatures could also enable living systems to use chemical species that would be too unstable at Earth temperatures to be useful.[51]

A set of conditions where ammonia is liquid at Earth-like temperatures would involve it being at a much higher pressure. For example, at 60 atm ammonia melts at −77 °C (196 K) and boils at 98 °C (371 K).[42]

Ammonia and ammonia–water mixtures remain liquid at temperatures far below the freezing point of pure water, so such biochemistries might be well suited to planets and moons orbiting outside the water-based habitability zone. Such conditions could exist, for example, under the surface of Saturn's largest moon Titan.[56]

Methane and other hydrocarbons

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Methane (CH4) is a simple hydrocarbon: that is, a compound of two of the most common elements in the cosmos: hydrogen and carbon. It has a cosmic abundance comparable with ammonia.[51] Hydrocarbons could act as a solvent over a wide range of temperatures, but would lack polarity. Isaac Asimov, the biochemist and science fiction writer, suggested in 1981 that poly-lipids could form a substitute for proteins in a non-polar solvent such as methane.[51] Lakes composed of a mixture of hydrocarbons, including methane and ethane, have been detected on the surface of Titan by the Cassini spacecraft.

There is debate about the effectiveness of methane and other hydrocarbons as a solvent for life compared to water or ammonia.[57][58][59] Water is a stronger solvent than the hydrocarbons, enabling easier transport of substances in a cell.[60] However, water is also more chemically reactive and can break down large organic molecules through hydrolysis.[57] A life-form whose solvent was a hydrocarbon would not face the threat of its biomolecules being destroyed in this way.[57] Also, the water molecule's tendency to form strong hydrogen bonds can interfere with internal hydrogen bonding in complex organic molecules.[50] Life with a hydrocarbon solvent could make more use of hydrogen bonds within its biomolecules.[57] Moreover, the strength of hydrogen bonds within biomolecules would be appropriate to a low-temperature biochemistry.[57]

Astrobiologist Chris McKay has argued, on thermodynamic grounds, that if life does exist on Titan's surface, using hydrocarbons as a solvent, it is likely also to use the more complex hydrocarbons as an energy source by reacting them with hydrogen, reducing ethane and acetylene to methane.[61] Possible evidence for this form of life on Titan was identified in 2010 by Darrell Strobel of Johns Hopkins University; a greater abundance of molecular hydrogen in the upper atmospheric layers of Titan compared to the lower layers, arguing for a downward diffusion at a rate of roughly 1025 molecules per second and disappearance of hydrogen near Titan's surface. As Strobel noted, his findings were in line with the effects Chris McKay had predicted if methanogenic life-forms were present.[60][61][62] The same year, another study showed low levels of acetylene on Titan's surface, which were interpreted by Chris McKay as consistent with the hypothesis of organisms reducing acetylene to methane.[60] While restating the biological hypothesis, McKay cautioned that other explanations for the hydrogen and acetylene findings are to be considered more likely: the possibilities of yet unidentified physical or chemical processes (e.g. a non-living surface catalyst enabling acetylene to react with hydrogen), or flaws in the current models of material flow.[63] He noted that even a non-biological catalyst effective at 95 K would in itself be a startling discovery.[63]

Azotosome

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A hypothetical cell membrane termed an azotosome, capable of functioning in liquid methane in Titan conditions was computer-modeled in an article published in February 2015. Composed of acrylonitrile, a small molecule containing carbon, hydrogen, and nitrogen, it is predicted to have stability and flexibility in liquid methane comparable to that of a phospholipid bilayer (the type of cell membrane possessed by all life on Earth) in liquid water.[64][65] An analysis of data obtained using the Atacama Large Millimeter / submillimeter Array (ALMA), completed in 2017, confirmed substantial amounts of acrylonitrile in Titan's atmosphere.[66][67] Later studies questioned whether acrylonitrile would be able to self-assemble into azotozomes.[68]

Hydrogen fluoride

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Hydrogen fluoride (HF), like water, is a polar molecule, and due to its polarity it can dissolve many ionic compounds. At atmospheric pressure, its melting point is 189.15 K (−84.00 °C), and its boiling point is 292.69 K (19.54 °C); the difference between the two is a little more than 100 K. HF also makes hydrogen bonds with its neighbor molecules, as do water and ammonia. It has been considered as a possible solvent for life by scientists such as Peter Sneath[69] and Carl Sagan.[49]

HF is dangerous to the systems of molecules that Earth-life is made of, but certain other organic compounds, such as paraffin waxes, are stable with it.[49] Like water and ammonia, liquid hydrogen fluoride supports an acid–base chemistry. Using a solvent system definition of acidity and basicity, nitric acid functions as a base when it is added to liquid HF.[70]

However, hydrogen fluoride is cosmically rare, unlike water, ammonia, and methane.[71]

Hydrogen sulfide

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Hydrogen sulfide is the closest chemical analog to water,[72] but is less polar and is a weaker inorganic solvent.[73] Hydrogen sulfide is quite plentiful on Jupiter's moon Io and may be in liquid form a short distance below the surface; astrobiologist Dirk Schulze-Makuch has suggested it as a possible solvent for life there.[74] On a planet with hydrogen sulfide oceans, the source of the hydrogen sulfide could come from volcanoes, in which case it could be mixed in with a bit of hydrogen fluoride, which could help dissolve minerals. Hydrogen sulfide life might use a mixture of carbon monoxide and carbon dioxide as their carbon source. They might produce and live on sulfur monoxide, which is analogous to oxygen (O2). Hydrogen sulfide, like hydrogen cyanide and ammonia, suffers from the small temperature range where it is liquid, though that, like that of hydrogen cyanide and ammonia, increases with increasing pressure.

Silicon dioxide and silicates

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Silicon dioxide, also known as silica and quartz, is very abundant in the universe and has a large temperature range where it is liquid. However, its melting point is 1,600 to 1,725 °C (2,912 to 3,137 °F), so it would be impossible to make organic compounds in that temperature, because all of them would decompose. Silicates are similar to silicon dioxide and some have lower melting points than silica. Feinberg and Shapiro have suggested that molten silicate rock could serve as a liquid medium for organisms with a chemistry based on silicon, oxygen, and other elements such as aluminium.[75]

Other solvents or cosolvents

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Sulfuric acid (H2SO4)

Other solvents sometimes proposed:

Sulfuric acid in liquid form is strongly polar. It remains liquid at higher temperatures than water, its liquid range being 10 °C to 337 °C at a pressure of 1 atm, although above 300 °C it slowly decomposes. Sulfuric acid is known to be abundant in the clouds of Venus, in the form of aerosol droplets. In a biochemistry that used sulfuric acid as a solvent, the alkene group (C=C), with two carbon atoms joined by a double bond, could function analogously to the carbonyl group (C=O) in water-based biochemistry.[43]

A proposal has been made that life on Mars may exist and be using a mixture of water and hydrogen peroxide as its solvent.[79] A 61.2% (by mass) mix of water and hydrogen peroxide has a freezing point of −56.5 °C and tends to super-cool rather than crystallize. It is also hygroscopic, an advantage in a water-scarce environment.[80][81]

Supercritical carbon dioxide has been proposed as a candidate for alternative biochemistry due to its ability to selectively dissolve organic compounds and assist the functioning of enzymes and because "super-Earth"- or "super-Venus"-type planets with dense high-pressure atmospheres may be common.[76]

Other speculations

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Non-green photosynthesizers

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Physicists have noted that, although photosynthesis on Earth generally involves green plants, a variety of other-colored plants could also support photosynthesis, essential for most life on Earth, and that other colors might be preferred in places that receive a different mix of stellar radiation than Earth.[82][83] These studies indicate that blue plants would be unlikely; however yellow or red plants may be relatively common.[83]

Variable environments

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Many Earth plants and animals undergo major biochemical changes during their life cycles as a response to changing environmental conditions, for example, by having a spore or hibernation state that can be sustained for years or even millennia between more active life stages.[84] Thus, it would be biochemically possible to sustain life in environments that are only periodically consistent with life as we know it.

For example, frogs in cold climates can survive for extended periods of time with most of their body water in a frozen state,[84] whereas desert frogs in Australia can become inactive and dehydrate in dry periods, losing up to 75% of their fluids, yet return to life by rapidly rehydrating in wet periods.[85] Either type of frog would appear biochemically inactive (i.e. not living) during dormant periods to anyone lacking a sensitive means of detecting low levels of metabolism.

Alanine world and hypothetical alternatives

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Early stage of the genetic code (GC-Code) with "alanine world" and its possible alternatives.

The genetic code may have evolved during the transition from the RNA world to a protein world.[86] The Alanine World Hypothesis postulates that the evolution of the genetic code (the so-called GC phase[87]) started with only four basic amino acids: alanine, glycine, proline and ornithine (now arginine).[88] The evolution of the genetic code ended with 20 proteinogenic amino acids. From a chemical point of view, most of them are Alanine-derivatives particularly suitable for the construction of α-helices and β-sheets – basic secondary structural elements of modern proteins. Direct evidence of this is an experimental procedure in molecular biology known as alanine scanning.

A hypothetical "Proline World" would create a possible alternative life with the genetic code based on the proline chemical scaffold as the protein backbone. Similarly, a "Glycine World" and "Ornithine World" are also conceivable, but nature has chosen none of them.[89] Evolution of life with Proline, Glycine, or Ornithine as the basic structure for protein-like polymers (foldamers) would lead to parallel biological worlds. They would have morphologically radically different body plans and genetics from the living organisms of the known biosphere.[90]

Nonplanetary life

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[dubious – discuss]

Dusty plasma-based

[edit]
See also: Dusty plasma

In 2007, Vadim N. Tsytovich and colleagues proposed that lifelike behaviors could be exhibited by dust particles suspended in a plasma, under conditions that might exist in space.[91][92] Computer models showed that, when the dust became charged, the particles could self-organize into microscopic helical structures, and the authors offer "a rough sketch of a possible model of...helical grain structure reproduction".

Cosmic necklace-based

[edit]

In 2020, Luis A. Anchordoqu and Eugene M. Chudnovsky of the City University of New York hypothesized that cosmic necklace-based life composed of magnetic monopoles connected by cosmic strings could evolve inside stars.[5] This would be achieved by a stretching of cosmic strings due to the star's intense gravity, thus allowing it to take on more complex forms and potentially form structures similar to the RNA and DNA structures found within carbon-based life. As such, it is theoretically possible that such beings could eventually become intelligent and construct a civilization using the power generated by the star's nuclear fusion. Because such use would use up part of the star's energy output, the luminosity would also fall. For this reason, it is thought that such life might exist inside stars observed to be cooling faster or dimmer than current cosmological models predict.

Life on a neutron star

[edit]

Frank Drake suggested in 1973 that intelligent life could inhabit neutron stars.[93] Physical models in 1973 implied that Drake's creatures would be microscopic.[citation needed]

Scientists who have published on this topic

[edit]

Scientists who have considered possible alternatives to carbon-water biochemistry include:

See also

[edit]

References

[edit]
  1. ^ David J. Des Marais; et al. (2008). "The NASA Astrobiology Roadmap". Astrobiology. 8 (4): 715–730. Bibcode:2008AsBio...8..715D. doi:10.1089/ast.2008.0819. PMID 18793098. S2CID 18725684.
  2. ^ Davila, Alfonso F.; McKay, Christopher P. (May 27, 2014). "Chance and Necessity in Biochemistry: Implications for the Search for Extraterrestrial Biomarkers in Earth-like Environments". Astrobiology. 14 (6): 534–540. Bibcode:2014AsBio..14..534D. doi:10.1089/ast.2014.1150. PMC 4060776. PMID 24867145.
  3. ^ Singer, Emily (July 19, 2015). "Chemists Invent New Letters for Nature's Genetic Alphabet". Wired. Retrieved July 20, 2015.
  4. ^ Kovač, Andreja; Majce, Vita; Lenaršič, Roman; Bombek, Sergeja; Bostock, Julieanne M.; Chopra, Ian; Polanc, Slovenko; Gobec, Stanislav (April 2007). "Diazenedicarboxamides as inhibitors of d-alanine-d-alanine ligase (Ddl)". Bioorganic & Medicinal Chemistry Letters. 17 (7): 2047–2054. doi:10.1016/j.bmcl.2007.01.015. PMID 17267218.
  5. ^ a b A. Anchordoqui, Luis; M. Chudnovsky, Eugene (31 March 2020). "Can Self-Replicating Species Flourish in the Interior of a Star?". Letters in High Energy Physics. 2020: 166. Bibcode:2020LHEP....3..166A. doi:10.31526/lhep.2020.166.
  6. ^ Tsytovich, V. N.; Morfill, G. E.; Fortov, V. E.; Gusein-Zade, N. G.; Klumov, B. A.; Vladimirov, S. V. (2007). "From plasma crystals and helical structures towards inorganic living matter". New Journal of Physics. 9 (8): 263. Bibcode:2007NJPh....9..263T. doi:10.1088/1367-2630/9/8/263. S2CID 123459022.
  7. ^ Hellingwerf, Klaas J.; Crielaard, Wim; Westerhoff, Hans V. (1993). "Comparison of Retinal-Based and Chlorophyll-Based Photosynthesis: A Biothermokinetic Description of Photochemical Reaction Centers". Modern Trends in Biothermokinetics. pp. 45–52. doi:10.1007/978-1-4615-2962-0_9. ISBN 978-1-4613-6288-3.
  8. ^ Banack, Sandra Anne; Metcalf, James S.; Jiang, Liying; Craighead, Derek; Ilag, Leopold L.; Cox, Paul Alan (2012). "Cyanobacteria Produce N-(2-Aminoethyl)Glycine, a Backbone for Peptide Nucleic Acids Which May Have Been the First Genetic Molecules for Life on Earth". PLOS ONE. 7 (11): e49043. Bibcode:2012PLoSO...749043B. doi:10.1371/journal.pone.0049043. PMC 3492184. PMID 23145061.
  9. ^ Hoshika S, Leal NA, Kim MJ, Kim MS, Karalkar NB, Kim HJ, Bates AM, Watkins NE, SantaLucia HA, Meyer AJ, DasGupta S, Ellington AD, SantaLucia J, Georgiadis MM, Benner SA (February 2019). "Hachimoji DNA and RNA: A genetic system with eight building blocks". Science. 363 (6429): 884–887. Bibcode:2019Sci...363..884H. doi:10.1126/science.aat0971. PMC 6413494. PMID 30792304.
  10. ^ "Hachimoji -- Expanding the genetic alphabet from four to eight". EurekAlert! (Press release). American Association for the Advancement of Science. 21 February 2019.
  11. ^ Davies, P. C. W.; Benner, S.A.; Cleland, C.E.; Lineweaver, C.H.; McKay, C.P.; Wolfe-Simon, F. (2009). "Signatures of a Shadow Biosphere". Astrobiology. 9 (2): 241–249. Bibcode:2009AsBio...9..241D. doi:10.1089/ast.2008.0251. PMID 19292603. S2CID 5723954.
  12. ^ Cleland, Carol E.; Copley, Shelley D. (16 January 2006). "The possibility of alternative microbial life on Earth". International Journal of Astrobiology. 4 (3–4): 165. Bibcode:2005IJAsB...4..165C. CiteSeerX 10.1.1.392.6366. doi:10.1017/S147355040500279X. S2CID 364892.
  13. ^ Davies, P.C.W.; Lineweaver, Charles H. (April 2005). "Finding a Second Sample of Life on Earth". Astrobiology. 5 (2): 154–163. Bibcode:2005AsBio...5..154D. doi:10.1089/ast.2005.5.154. PMID 15815166.
  14. ^ Sagan, Carl; Agel, Jerome (2000). Carl Sagan's Cosmic Connection: an Extraterrestrial Perspective (2nd ed.). Cambridge U.P. p. 41. ISBN 978-0-521-78303-3.
  15. ^ a b Sagan, Carl (2000). Carl Sagan's Cosmic Connection: an Extraterrestrial Perspective (2nd ed.). Cambridge U.P. p. 46.
  16. ^ Sagan, Carl (2000). Carl Sagan's Cosmic Connection: an Extraterrestrial Perspective (2nd ed.). Cambridge U.P. p. 47.
  17. ^ a b Horowitz, N.H. (1986). Utopia and Back and the search for life in the solar system. New York: W.H. Freeman and Company. ISBN 0-7167-1766-2.[page needed]
  18. ^ a b c Pace, N. R. (2001). "The universal nature of biochemistry". Proceedings of the National Academy of Sciences of the United States of America. 98 (3): 805–808. Bibcode:2001PNAS...98..805P. doi:10.1073/pnas.98.3.805. PMC 33372. PMID 11158550.
  19. ^ a b "Astrobiology". Biology Cabinet. September 26, 2006. Archived from the original on 2010-12-12. Retrieved 2011-01-17.
  20. ^ Lazio, Joseph. "F.10 Why do we assume that other beings must be based on carbon? Why couldn't organisms be based on other substances?". [sci.astro] ET Life (Astronomy Frequently Asked Questions). Retrieved 2006-07-21.
  21. ^ a b c d Bains 2004.
  22. ^ a b Gillette, Stephen (1996). World-Building. Writer's Digest Books. ISBN 978-0-89879-707-7.
  23. ^ William Bains. "The nature of life". Astrobiology. Archived from the original on 27 Jan 2019. Retrieved 2015-03-20.
  24. ^ Cairns-Smith, A. Graham (1985). Seven Clues to the Origin of Life. Cambridge: Cambridge University Press. ISBN 978-0-521-27522-4.
  25. ^ Dawkins, Richard (1996) [1986]. The Blind Watchmaker. New York: W. W. Norton & Company, Inc. pp. 148–161. ISBN 978-0-393-31570-7.
  26. ^ Kan, S. B. Jennifer; Lewis, Russell D.; Chen, Kai; Arnold, Frances H. (25 November 2016). "Directed evolution of cytochrome c for carbon–silicon bond formation: Bringing silicon to life". Science. 354 (6315): 1048–1051. Bibcode:2016Sci...354.1048K. doi:10.1126/science.aah6219. PMC 5243118. PMID 27885032.
  27. ^ a b "Life-like cells are made of metal". New Scientist. September 14, 2011. Retrieved 2014-05-25.
  28. ^ Philippot, Pascal; Van Zuilen, Mark; Lepot, Kevin; Thomazo, Christophe; Farquhar, James; Van Kranendonk, Martin J. (14 September 2007). "Early Archaean Microorganisms Preferred Elemental Sulfur, Not Sulfate". Science. 317 (5844): 1534–1537. Bibcode:2007Sci...317.1534P. doi:10.1126/science.1145861. PMID 17872441.
  29. ^ "Biochemical Periodic Table – Arsenic". UMBBD. 2007-06-08. Retrieved 2010-05-29.
  30. ^ Niggemyer, Allison; Spring, Stefan; Stackebrandt, Erko; Rosenzweig, R. Frank (December 2001). "Isolation and Characterization of a Novel As(V)-Reducing Bacterium: Implications for Arsenic Mobilization and the Genus Desulfitobacterium". Applied and Environmental Microbiology. 67 (12): 5568–5580. Bibcode:2001ApEnM..67.5568N. doi:10.1128/AEM.67.12.5568-5580.2001. PMC 93345. PMID 11722908.
  31. ^ Reilly, Michael (April 2008). "Early life could have been based on arsenic". New Scientist. 198 (2653): 10. doi:10.1016/S0262-4079(08)61007-6.
  32. ^ Westheimer, F. H. (6 March 1987). "Why Nature Chose Phosphates". Science. 235 (4793): 1173–1178. Bibcode:1987Sci...235.1173W. doi:10.1126/science.2434996. PMID 2434996.
  33. ^ "NASA-Funded Research Discovers Life Built With Toxic Chemical". NASA.gov. 2 December 2010. Archived from the original on 2011-08-28. Retrieved 2010-12-02.
  34. ^ a b Wolfe-Simon, Felisa; Blum, Jodi Switzer; Kulp, Thomas R.; Gordon, Shelley E.; Hoeft, S. E.; Pett-Ridge, Jennifer; Stolz, John F.; Webb, Samuel M.; Weber, Peter K.; Davies, Paul C. W.; Anbar, Ariel D.; Oremland, Ronald S. (2 December 2010). "A Bacterium That Can Grow by Using Arsenic Instead of Phosphorus". Science. 332 (6034): 1163–6. Bibcode:2011Sci...332.1163W. doi:10.1126/science.1197258. PMID 21127214. S2CID 51834091.
  35. ^ Redfield, Rosemary (4 December 2010). "Arsenic-associated bacteria (NASA's claims)". rrresearch.blogspot.com/. Retrieved 4 December 2010.[self-published source?]
  36. ^ Bradley, Alex (5 December 2010). "Arsenate-based DNA: a big idea with big holes". scienceblogs.com/webeasties/. Archived from the original on 8 December 2010. Retrieved 9 December 2010.
  37. ^ Zimmer, Carl (7 December 2010). "Scientists see fatal flaws in the NASA study of arsenic-based life". Slate. Retrieved 7 December 2010.
  38. ^ Williams, Sarah (7 November 2012). ""Arsenic Life" Claim Refuted". BioTechniques. Archived from the original on 4 March 2016. Retrieved 23 January 2013.
  39. ^ Basturea GN, Harris TK and Deutscher MP (17 August 2012). "Growth of a bacterium that apparently uses arsenic instead of phosphorus is a consequence of massive ribosome breakdown". J Biol Chem. 287 (34): 28816–9. doi:10.1074/jbc.C112.394403. PMC 3436571. PMID 22798070.
  40. ^ Benner, Steven A.; Ricardo, Alonso; Carrigan, Matthew A (2004). "Is there a common chemical model for life in the universe?". Current Opinion in Chemical Biology. 8 (6): 676–680. doi:10.1016/j.cbpa.2004.10.003. PMID 15556414.
  41. ^ Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; pages 69–79.
  42. ^ a b c d e Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; p. 72.
  43. ^ a b c Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; p. 73.
  44. ^ a b c Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; p. 74.
  45. ^ a b c Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; p. 75.
  46. ^ Benner, Steven A.; Hutter, Daniel (February 2002). "Phosphates, DNA, and the Search for Nonterrean Life: A Second Generation Model for Genetic Molecules". Bioorganic Chemistry. 30 (1): 62–80. doi:10.1006/bioo.2001.1232. PMID 11955003.
  47. ^ Sagan, Carl (2002). Cosmos. Random House. pp. 126–127. ISBN 978-0-375-50832-5.
  48. ^ a b c Sagan, Carl; Head, Tom (2006). Conversations with Carl Sagan. University Press of Mississippi. p. 10. ISBN 978-1-57806-736-7.
  49. ^ a b c d Sagan, Carl (2002). Cosmos. Random House. p. 128. ISBN 978-0-375-50832-5.
  50. ^ a b c d Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; page 70.
  51. ^ a b c d e f Isaac Asimov (Winter 1981). "Not as We Know it – the Chemistry of Life". Cosmic Search (9 (Vol 3 No 1)). North American AstroPhysical Observatory.
  52. ^ a b J. B. S. Haldane (1954). "The Origins of Life". New Biology. 16: 12–27. cited in Darling, David. "Ammonia-based life". Archived from the original on 2012-10-18. Retrieved 2012-10-01.
  53. ^ a b c Darling, David. "ammonia-based life". Retrieved 2012-10-01.
  54. ^ Feinberg, Gerald; Robert Shapiro (1980). Life Beyond Earth. Morrow. ISBN 978-0-688-03642-3. cited in Darling, David. "ammonia-based life". Archived from the original on 2012-10-18. Retrieved 2012-10-01.
  55. ^ a b Schulze-Makuch, Dirk; Irwin, Louis Neal (2008). Life in the Universe: Expectations and Constraints (2 ed.). Springer. p. 119. ISBN 978-3-540-76816-6.
  56. ^ Fortes, A. D. (1999). "Exobiological Implications of a Possible Ammonia-Water Ocean Inside Titan". Retrieved 7 June 2010.
  57. ^ a b c d e Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; page 74.
  58. ^ McLendon, Christopher; Opalko, F. Jeffrey (March 2015). "Solubility of Polyethers in Hydrocarbons at Low Temperatures. A Model for Potential Genetic Backbones on Warm Titans". Astrobiology. 15 (3): 200–206. Bibcode:2015AsBio..15..200M. doi:10.1089/ast.2014.1212. PMID 25761113.
  59. ^ Hadhazy, Adam (13 May 2015). "Alien Life on Oily Exoplanets Could Have Ether-based 'DNA'". Astrobiology Magazine. Space.com. Retrieved 2015-05-21.
  60. ^ a b c "What is Consuming Hydrogen and Acetylene on Titan?". NASA/JPL. 2010. Archived from the original on June 29, 2011. Retrieved 2010-06-06.
  61. ^ a b McKay, C. P.; Smith, H. D. (2005). "Possibilities for methanogenic life in liquid methane on the surface of Titan". Icarus. 178 (1): 274–276. Bibcode:2005Icar..178..274M. doi:10.1016/j.icarus.2005.05.018.
  62. ^ Strobel, Darrell F. (August 2010). "Molecular hydrogen in Titan's atmosphere: Implications of the measured tropospheric and thermospheric mole fractions". Icarus. 208 (2): 878–886. Bibcode:2010Icar..208..878S. doi:10.1016/j.icarus.2010.03.003.
  63. ^ a b Mckay, Chris (2010). "Have We Discovered Evidence For Life On Titan". New Mexico State University. Archived from the original on 2016-03-09. Retrieved 2014-05-15.
  64. ^ Stevenson, James; Lunine, Jonathan; Clancy, Paulette (27 Feb 2015). "Membrane alternatives in worlds without oxygen: Creation of an azotosome". Science Advances. 1 (1): e1400067. Bibcode:2015SciA....1E0067S. doi:10.1126/sciadv.1400067. PMC 4644080. PMID 26601130.
  65. ^ Life 'not as we know it' possible on Saturn's moon Titan.
  66. ^ Wall, Mike (28 July 2017). "Saturn Moon Titan Has Molecules That Could Help Make Cell Membranes". Space.com. Retrieved 29 July 2017.
  67. ^ Palmer, Maureen Y.; et al. (28 July 2017). "ALMA detection and astrobiological potential of vinyl cyanide on Titan". Science Advances. 3 (7): e1700022. Bibcode:2017SciA....3E0022P. doi:10.1126/sciadv.1700022. PMC 5533535. PMID 28782019.
  68. ^ Sandström, H.; Rahm, M. (January 2020). "Can polarity-inverted membranes self-assemble on Titan?". Science Advances. 6 (4): eaax0272. Bibcode:2020SciA....6..272S. doi:10.1126/sciadv.aax0272. PMC 6981084. PMID 32042894.
  69. ^ a b Sneath, P. H. A. (1970). Planets and Life. Thames and Hudson. cited in Boyce, Chris (1981). Extraterrestrial Encounter. New English Library. pp. 125, 182.
  70. ^ Jander, Gerhart; Spandau, Hans; Addison, C. C. (1971). Chemistry in Nonaqueous Ionizing solvents: Inorganic Chemistry in Liquid Hydrogen Cyanide and Liquid hydrogen Fluoride. Vol. II. N.Y.: Pergamon Press. cited in Freitas, Robert A. (1979). "8.2.2". Xenology: An Introduction to the Scientific Study of Extraterrestrial Life, Intelligence, and Civilization. Sacramento, CA: Xenology Research Institute.
  71. ^ Freitas, Robert A. (1979). "8.2.2". Xenology: An Introduction to the Scientific Study of Extraterrestrial Life, Intelligence, and Civilization. Sacramento, CA: Xenology Research Institute.
  72. ^ Darling, David. "solvent". Retrieved 2012-10-12.
  73. ^ Jander, J.; Lafrenz, C. (1970). Ionizing Solvents. Vol. I. Weinheim/Bergstr.: John Wiley & Sons Ltd., Verlag Chemie. cited in Freitas, Robert A. (1979). "8.2.2". Xenology: An Introduction to the Scientific Study of Extraterrestrial Life, Intelligence, and Civilization. Sacramento, CA: Xenology Research Institute.
  74. ^ Choi, Charles Q. (2010-06-10). "The Chance for Life on Io". Archived from the original on 2012-10-27. Retrieved 2013-05-25.{{cite web}}: CS1 maint: unfit URL (link)
  75. ^ David W. Koerner; Simon LeVay (2000). Here Be Dragons : The Scientific Quest for Extraterrestrial Life. Oxford U.P. p. 202. ISBN 978-0-19-803337-0.
  76. ^ a b Budisa, Nediljko; Schulze-Makuch, Dirk (8 August 2014). "Supercritical Carbon Dioxide and Its Potential as a Life-Sustaining Solvent in a Planetary Environment". Life. 4 (3): 331–340. Bibcode:2014Life....4..331B. doi:10.3390/life4030331. PMC 4206850. PMID 25370376.
  77. ^ a b Ward, Peter D.; Benner, Steven A. (2007). "Alien biochemistries". In Sullivan, Woodruff T.; Baross, John A. (eds.). Planets and Life. Cambridge: Cambridge. p. 540. ISBN 978-0-521-53102-3.
  78. ^ The methane habitable zone.
  79. ^ Houtkooper, Joop M.; Dirk Schulze-Makuch (2007-05-22). "A Possible Biogenic Origin for Hydrogen Peroxide on Mars". International Journal of Astrobiology. 6 (2): 147. arXiv:physics/0610093. Bibcode:2007IJAsB...6..147H. doi:10.1017/S1473550407003746. S2CID 8091895.
  80. ^ Houtkooper, Joop M.; Dirk Schulze-Makuch (2007). "The H2O2–H2O Hypothesis: Extremophiles Adapted to Conditions on Mars?" (PDF). EPSC Abstracts. 2: 558. Bibcode:2007epsc.conf..558H. EPSC2007-A-00439. Archived (PDF) from the original on 2007-09-26.
  81. ^ Ellison, Doug (2007-08-24). "Europlanet : Life's a bleach". Planetary.org. Archived from the original on 2010-09-25. Retrieved 2007-08-25.
  82. ^ "NASA – NASA Predicts Non-Green Plants on Other Planets". Nasa.gov. 2008-02-23. Retrieved 2010-05-29.
  83. ^ a b Kiang, Nancy Y.; Segura, Antígona; Tinetti, Giovanna; Jee, Govind; Blankenship, Robert E.; Cohen, Martin; Siefert, Janet; Crisp, David; Meadows, Victoria S. (2007-04-03). "Spectral signatures of photosynthesis. II. Coevolution with other stars and the atmosphere on extrasolar worlds". Astrobiology. 7 (1): 252–274. arXiv:astro-ph/0701391. Bibcode:2007AsBio...7..252K. doi:10.1089/ast.2006.0108. PMID 17407410. S2CID 9172251.
  84. ^ a b "Christmas in Yellowstone". Pbs.org. Archived from the original on 2008-10-08. Retrieved 2010-05-29.
  85. ^ Main, A. R.; Bentley, P. J. (1964). "Main and Bentley, Ecology, "Water Relations of Australian Burrowing Frogs and Tree Frogs" (1964)". Ecology. 45 (2): 379–382. doi:10.2307/1933854. JSTOR 1933854.
  86. ^ Doig, Abdrew J. (7 December 2016). "Frozen, but no accident – why the 20 standard amino acids were selected". FEBS J. 284 (9): 1296–1305. doi:10.1111/febs.13982. PMID 27926995.
  87. ^ Hartman, Hyman; Smith, Temple F. (20 May 2014). "The Evolution of the Ribosome and the Genetic Code". Life. 4 (2): 227–249. Bibcode:2014Life....4..227H. doi:10.3390/life4020227. PMC 4187167. PMID 25370196.
  88. ^ Kubyshkin, Vladimir; Budisa, Nediljko (24 September 2019). "The Alanine World Model for the Development of the Amino Acid Repertoire in Protein Biosynthesis". Int. J. Mol. Sci. 20 (21): 5507. doi:10.3390/ijms20215507. PMC 6862034. PMID 31694194.
  89. ^ Kubyshkin, Vladimir; Budisa, Nediljko (3 July 2019). "Anticipating alien cells with alternative genetic codes: away from the alanine world!". Curr. Opin. Biotechnol. 60: 242–249. doi:10.1016/j.copbio.2019.05.006. PMID 31279217.
  90. ^ Budisa, Nediljko; Kubyshkin, Vladimir; Schmidt, Markus (22 April 2020). "Xenobiology: A Journey towards Parallel Life Forms". ChemBioChem. 21 (16): 2228–2231. doi:10.1002/cbic.202000141. PMID 32323410.
  91. ^ "Physicists Discover Inorganic Dust With Lifelike Qualities". ScienceDaily (Press release). Institute of Physics. 15 August 2007.
  92. ^ Tsytovich, V N; G E Morfill, V E Fortov, N G Gusein-Zade, B A Klumov and S V Vladimirov; Fortov, V E; Gusein-Zade, N G; Klumov, B A; Vladimirov, S V (14 August 2007). "From plasma crystals and helical structures towards inorganic living matter". New J. Phys. 9 (263): 263. Bibcode:2007NJPh....9..263T. doi:10.1088/1367-2630/9/8/263.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  93. ^ Drake, F.D. (December 1973). "Life on a Neutron Star: An Interview with Frank Drake" (PDF). Astronomy: 5–8. Archived (PDF) from the original on 2021-03-15.
  94. ^ V. Axel Firsoff (January 1962). "An Ammonia-Based Life". Discovery. 23: 36–42. cited in Darling, David. "ammonia-based life". Archived from the original on 2012-10-18. Retrieved 2012-10-01.
  95. ^ a b Shklovskii, I.S.; Carl Sagan (1977). Intelligent Life in the Universe. Picador. p. 229.
  96. ^ Feinberg, Gerald; Robert Shapiro (1980). Life Beyond Earth. Morrow. ISBN 978-0-688-03642-3.[page needed]
  97. ^ A detailed review of this book is: John Gribbin (2 Oct 1980). "Life beyond Earth". New Scientist: xvii.
  98. ^ Freitas, Robert A. (1979). Xenology: An Introduction to the Scientific Study of Extraterrestrial Life, Intelligence, and Civilization. Sacramento, CA: Xenology Research Institute.
  99. ^ This work is acknowledged the partial basis of the article Darling, David. "ammonia-based life". Archived from the original on 2012-10-18. Retrieved 2012-10-01.
  100. ^ Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007.
  101. ^ Committee on the Limits of Organic Life in Planetary Systems, Committee on the Origins and Evolution of Life, National Research Council; The Limits of Organic Life in Planetary Systems; The National Academies Press, 2007; page 5

Further reading

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