Life/Citable Version: Difference between revisions
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What is '''life'''? Biologists use the word 'life' for both the processes of living, and for the things that carry out those processes. Life, too, connotes the relationships among living things, past and present: it includes the entire living world — the biosphere — and the whole history of | What is '''life'''? Biologists use the word 'life' for both the processes of living, and for the things that carry out those processes. Life, too, connotes the relationships among living things, past and present: it includes the entire living world — the biosphere — and the whole history of 'life on earth'. In theory, life might include entities, now unknown, that exist on other planets. Just what qualities would such beings have to possess for scientists to acknowledge them ''as'' alive? Could ''non''-living things ever acquire those same qualities? What features separated the first living cells from the inanimate materials that formed them? The answers to such questions form part of the larger answer to that most basic of all questions in [[Biology]]: "what is life?" This article focuses not on 'life', the noun, but on 'living', the verb; on what activities living entities perform, and on the processes that enable their performance.<ref>'''Note:''' Some words, so-called ‘[[semantic primes]]’ have distinct meanings not definable in terms of other words. Ultimately, all definitions converge on about 70 semantic primes that occur universally among languages. Semantic primes include the verb ‘live’ but not the noun ‘life’. [http://www.ali2006.une.edu.au/GoddardWierzbicka_applied_NSM.pdf (Semantic Primes and Cultural Scripts in Language: Learning and Intercultural Communication.)]<br>Carol Cleland of [[NASA]]’s [http://nai.arc.nasa.gov/ Astrobiology Institute] suggests that scientists are not really interested in what the word 'life' happens to mean in our language. "What we really need to focus on is coming up with an adequately general theory of living systems, as opposed to a definition of 'life'."[http://www.astrobio.net/news/article2176.html Carol Cleland on "What is Life?"]</ref> It takes, as its theme, “Life is what is common to all living beings” (''Christian De Duve'').<ref>De Duve C (2004) ''Life Evolving: Molecules, Mind, and Meaning.'' Oxford University Press. New York ISBN 0195156056</ref> | ||
(see also [[Biology]] and [[Systems biology]]). | (see also [[Biology]] and [[Systems biology]]). | ||
[[Image: | [[Image:Plants and pollinators.jpg|thumb|350px|Buzz of Life: One aspect of the interrelations among living entities. Researchers begin to understand the mechanisms governing the complex network interactions between plants and pollinators, such as hummingbirds, shown in this illustration from Ernst Haeckel's ''Kunstformen der Natur'' (1904).<ref>from Robinson R (2007) Both barriers and trait complementarity govern pollination network structure. PLoS Biol 5(2): e54 doi:10.1371/journal.pbio.0050054</ref>]] | ||
==Principles of life== | ==Principles of life== | ||
===Molecules=== | ===Molecules=== | ||
All known life is built from the same set of [[Organic chemistry|organic molecules]] | :''See related topics: [[Chemistry]], [[Biochemistry]], and [[Organic chemistry|Organic Chemistry]]'' | ||
All known life is built from the same set of [[Organic chemistry|organic molecules]]. Although they contain many elements, organic molecules always have a predominant structure of carbon linked to itself. In living things, organic species exist in mixtures of [[colloid|colloidal]] ''[[aqueous]]'' solutions that are never completely homogeneous but are bounded by [[lipid]] and [[protein]] sheets. Each pool can have a different composition with distinct properties of [[charge]], [[density]], [[viscosity]] and [[osmotic pressure]]; these differences provide the basis for the generation of electric fields, fluid shifts, and transport of molecules. The stuff of life, then, is carbon chains, studded with other atoms, and arranged in lagoons of fat, water, and salts. | |||
===Cells=== | ===Cells=== | ||
As well as sharing a common carbon- and water-based chemistry, every entity that [[Biology |biologists]] ''acknowledge'' as living — bacteria, trees, fish, chimpanzees — shares a common building block, the [[cell]]. Cells are universally enclosed in a membrane (a [[phospholipid]] bilayer known as the [[cytoplasmic membrane]]), that separates the inside of the cell from the external environment. Interestingly, the chemistry of the cell membrane is ''not'' universal. In | :''See Related Topics: [[Cell biology|Cell Biology]], [[Microbiology]]'' | ||
As well as sharing a common carbon- and water-based chemistry, every entity that [[Biology |biologists]] ''acknowledge'' as living — bacteria, trees, fish, chimpanzees — shares a common building block, the [[cell]]. Cells are universally enclosed in a membrane (a [[phospholipid]] bilayer known as the [[cytoplasmic membrane]]), that separates the inside of the cell from the external environment. Interestingly, the chemistry of the cell membrane is ''not'' universal. In most types of cells the molecules of the membrane are based on ''esters'' of glycerol combined with straight chain [[fatty acid]]s, but in the ''[[Archaea]]'' the chemistry of membranes is based on glycerol ''ether'' linkages and isoprene fatty components. | |||
Many organisms live as single cells, | Many organisms live as isolated single cells, others form cooperative colonies of cells, and still other cells are members of complex multicellular systems that include diverse cell types, each specialized for different functions.<ref>Valentine JW ''et al.'' (1994) Morphological complexity increase in metazoans. Paleobiology [http://links.jstor.org/sici?sici=0094-8373%28199421%2920%3A2%3C131%3AMCIIM%3E2.0.CO%3B2-B 20:131-42]</ref> Nature has produced an enormous variety of cell types that span three vast ‘domains’ of living systems: ''[[Archaea]]'', ''[[Bacteria]]'', and ''[[Eukarya]]'',<ref name=woese90pnas>Woese CR ''et al.'' (1990) Towards a natural system of organisms: proposal for the domains archaea, bacteria, and eucarya. Proc Natl Acad Sci USA 87:[http://dx.doi.org/10.1073/pnas.87.12.4576 4576-9]</ref> yet cells in all three domains have many features in common. All cells have a surrounding membrane; a physical boundary that separates them from their environment. The surface of that membrane always has special properties that allow protection, excretion, ingestion or communication. Often, these functions are provided by changes in the shape or actual chemical species present on the surface — so pores, [[receptor molecule]]s and protective walls are often features of the cell surface. This is true in both unicellular and multicellular entities.<ref>'''Note''': Other boundaries of living systems include bark, shells, cell walls, skin, fur, and structures of the physical environment.</ref> | ||
Current evidence indicates that only pre-existing cells can ‘manufacture’ cells. So how did the [[Origin of life|first]] [[Evolution of cells| cell(s)]] arise? | |||
Examining what all extant cells have in common may provide insight to the [[Origin of life]]. All extract chemical energy from simple oxidation reactions, and convert it into other, chemical forms of energy. The molecule [[ATP]] universally serves as the cell's main energy 'currency'. All cells inherit digitally stored information in the form of molecules of [[DNA]], and with minor exceptions the DNA of all cells use the same universal [[genetic code]] to guide production of a myriad of distinct [[protein]] structures. Cells use those proteins to carry out diverse activities, including energy processing and conversion of carbon, nitrogen and phosphorous-containing materials into cellular structures. In the human [[genome]], perhaps as few as 22,000 different protein-coding genes<ref>[http://www.ornl.gov/sci/techresources/Human_Genome/faq/genenumber.shtml ''How Many Genes Are in the Human Genome?''] at the Human Genome Project Information website hosted by the U.S. Department of Energy</ref> lead to the production of perhaps more than a million distinct protein structures that make up the variety and quantity of protein molecules needed for the structures and functions of a cell. Numerous molecular mechanisms account for that quantitative gene-to-protein amplification.<ref>'''(a)''' The UniProtKB/Swiss-Prot Human Proteome Initiative [http://ca.expasy.org/sprot/hpi/hpi_desc.html]; '''(b)''' Norregaard Jensen O. (2004) Modification-specific proteomics: characterization of post-translational modifications by mass spectrometry. Current Opinion in Chemical Biology [http://dx.doi.org/10.1016/j.cbpa.2003.12.009 8:33-41]</ref> | |||
Nature has produced a huge diversity of single-celled organisms and large, complex animals or plants. The latter can contain vast numbers of cells, each part of a specialized subpopulation (cell types) — in a mammal, the cells that make up bone differ from those that make up muscle, and differ again from those that make up skin, for example. Humans contain approximately 200 different cell types as classified by microscopic anatomy.<ref>Valentine JW ''et al.'' (1994) Morphological complexity increase in metazoans. Paleobiology [http://links.jstor.org/sici?sici=0094-8373%28199421%2920%3A2%3C131%3AMCIIM%3E2.0.CO%3B2-B 20:131-42]<br>'''Note''': See the article, Cell, for a more thorough discussion of 'cell types'.</ref> In multicellular organisms, cells combine to make organs, the functional and structural components of the single larger organism. | |||
So what makes a single celled organism 'alive', and | So what makes a single celled organism 'alive', and does the answer apply also when we call a large complex multicellular animal or plant 'alive'? What exactly do we mean by 'living'? | ||
===Systems view of 'living'=== | ===Systems view of 'living'=== | ||
''(See main article, [[Systems biology]])'' | ''(See main article, [[Systems biology]])'' | ||
[[Image:Acrosome_reaction_diagram_svg.png|thumb|400px|left|Oocyte and spermatozoon merging to begin a new living system.]] | [[Image:Acrosome_reaction_diagram_svg.png|thumb|400px|left|Oocyte and spermatozoon merging to begin a new living system.]] | ||
[[Ernst Mayr]] | The evolutionary biologist [[Ernst Mayr]] suggested that, to define 'life', we need to clarify what we mean by the process of 'living': | ||
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The | The systems perspective of 'living' recalls [[Aristotle]]'s four components of causality,<ref>Andrea Falcon (2006) [http://plato.stanford.edu/entries/aristotle-causality/ ''Aristotle on Causality'']</ref> <ref>Bothwell JHF. (2006) The long past of systems biology. New Phytologist 170:6-10 [http://dx.doi.org/10.1111/j.1469-8137.2006.01676.x Link to Full-Text].<br>'''Note''': We might interpret Aristotle's four components of 'causality' as four components of 'explanation', for as Bothwell writes: “Aristotle (384-322 BC) wanted to search for explanations of natural events that inspire wonder. His search led him to conclude that any question which might be asked about the behaviour of a complex, apparently designed, system might be answered if we knew four properties of that system. He called these the aitiai, a word which is usually rendered into English as 'causes', but which may be better translated as 'explanations' (Aristotle, APst 90a7-94b34; CA 715a1-17 [Aristotle. APst (Posterior Analytics), Trans: H. Tredennick (1960). Harvard University Press, Loeb Classical Library. (ISBN 0-674-99430-2)]).”</ref> in that a living thing comprises: | ||
:* A list of organic and inorganic parts ([[molecules]] and [[ions]]; [[cells]], organelles, [[organs]] and organisms) — ''Aristotle’s 'material' cause''; | :* A list of organic and inorganic parts ([[molecules]] and [[ions]]; [[cells]], organelles, [[organs]] and organisms) — ''Aristotle’s 'material' cause''; | ||
:* How the parts relate to each other to form structures (e.g., networks), how they interact with each other (e.g., network dynamics), and how the structures interact with each other in a coordinated dynamic and hierarchical manner — ''Aristotle’s 'formal' (form-like) cause''; | :* How the parts relate to each other to form structures (e.g., networks), how they interact with each other (e.g., network dynamics), and how the structures interact with each other in a coordinated dynamic and hierarchical manner — ''Aristotle’s 'formal' (form-like) cause''; | ||
:* How the parts and structures became | :* How the parts and structures became dynamically coordinated (e.g., gene expression; self-organization; competition) — ''Aristotle’s 'efficient' (effect-producing) cause''; and | ||
:* How the living system as-a-whole functions and behaves, and the properties that characterize it (e.g., reproduction; locomotion; cognition) — ''Aristotle’s 'final' cause'' | :* How the living system as-a-whole functions and behaves, and the properties that characterize it (e.g., reproduction; locomotion; cognition) — ''Aristotle’s 'final' cause'' | ||
The analysis of all of those components together forms part of | The analysis of all of those components together forms part of the new discipline of [[Systems biology|Systems Biology]]. Systems biologists study, among other things, the phenomenon of '[[emergence]]', whereby properties, functions, and behaviors of living systems arise though not exhibited by ''any'' individual component of the system, and not predictable from complete understanding the components' behaviors alone considered in isolation from the system that embeds them. Every cellular system exhibits emergent behaviors. Emergent behaviors of living systems include such things as locomotion, sexual display, flocking, and conscious experiencing. | ||
Why | Why do not all of the properties of a system predictably result from the properties of its components? After all, the [[reductionist]] paradigm that dominated the [[Scientific method]] in the 20th century operated on the exactly opposite assumption. For one thing, the intrinsic properties of a system’s components themselves do ''not'' determine those of the whole system; rather, their 'organizational dynamics' does, and those dynamics include not only the interrelations among the components themselves, but also interactions among the many different organizational units in the system. <ref>'''Note''': For example, physical chemists cannot predict the properties of water from knowledge of its components, hydrogen and oxygen. The way hydrogen and water interact to form H<sub>2</sub>O, and the way H<sub>2</sub>O molecules interact, enables the properties of water to 'emerge'.</ref> Secondly, the living system always operates in a context (its external environment, or surroundings), and that, in turn, always affects the properties of the system-as-a-whole. For example, nutrient gradients influence the direction a bacterium’s locomotion. The impact of environmental context affects the organization of the components within the system — a 'downward causation'. <ref>'''Note''': Following up on the example of water, the properties of its environment (e.g., temperature, pressure) affect the way the H<sub>2</sub>O molecules organize themselves, as ice, or liquid, or steam</ref> For another example, environmental signals can activate or suppress a metabolic pathway, reorganizing cellular activity<ref>'''Note''': In relation to downward causation, the environment’s effect can sometimes reach down to the genetic recipe with molecular signals, altering the recipe’s expression and consequently the characteristics of the cells — so-called 'epigenetic' effects. When [[epigenetic]] alterations of [[gene expression]] occur in the [[reproductive system|reproductive organs]], the system changes can be transmitted to the next generation. See | ||
:Jablonka E, Lamb MJ (2005) ''Evolution in Four Dimension: Genetic, Epigenetic, Behavioral, and Symbolic Variation in the History of Life.'' Cambridge: MIT Press | :*Jablonka E, Lamb MJ (2005) ''Evolution in Four Dimension: Genetic, Epigenetic, Behavioral, and Symbolic Variation in the History of Life.'' Cambridge: MIT Press | ||
:Gorelick R (2004) Neo-Lamarckian medicine. Med Hypotheses 62:299-303 PMID 14962644</ref> | :*Gorelick R (2004) Neo-Lamarckian medicine. Med Hypotheses 62:299-303 PMID 14962644</ref> One cannot simply take a living system apart and predict how it will behave. | ||
Philosopher of science D.M. Walsh puts it this way: "The constituent parts and processes of a living thing are related to the organism as a whole by a kind of 'reciprocal causation'."<ref>Walsh DM (2006) Organisms as natural purposes: the contemporary evolutionary perspective. Stud Hist Philos Biol Biomed Sci 37: [http://dx.doi.org/doi:10.1016/j.shpsc.2006.09.009 771-91]</ref> In other words, the organization of the components determine the behavior of the system, but that organization arises from more than the set of its internal components. How the system behaves as it interacts with its environment determines how | Philosopher of science D.M. Walsh puts it this way: "The constituent parts and processes of a living thing are related to the organism as a whole by a kind of 'reciprocal causation'."<ref>Walsh DM (2006) Organisms as natural purposes: the contemporary evolutionary perspective. Stud Hist Philos Biol Biomed Sci 37: [http://dx.doi.org/doi:10.1016/j.shpsc.2006.09.009 771-91]</ref> In other words, the organization of the components determine the behavior of the system, but that organization arises from more than the set of its internal components. How the whole system behaves as it interacts with its environment determines how those components organize themselves, and so novel properties of the system 'emerge' that characterize neither the environment nor that set of internal components. For example, the behavior of a human kidney cell depends not only on its cellular physiology, but also on all the properties of the organ ([[kidney]]) which constitutes its environment. The kidney's overall structure and function influence the cell’s structure and behavior (e.g., by physical confinement and by cell-to-cell signaling), which in turn influence the organization of its intracellular components. The kidney in turn responds to ''its'' environment, namely the individual body that it lives in, and that body responds to ''its'' environment, which includes such factors as the availability of particular food items, fresh water, and ambient [[temperature]] and [[humidity]]. Systems biologists regard emergent properties as arising from from a combination of ''bottom-up'' and ''top-down'' effects — Walsh's 'reciprocal causation'. | ||
Other basic concepts that systems biologists consider crucial in explaining living systems as-a-whole include 'robustness', 'modularity', and 'networks' — all discussed in sections below. Quantitative modeling and simulation guided by experimental biological data provide the mainstay methodologies of systems biologists. (See [[Systems biology]]) | |||
===The thermodynamics of 'living'=== | ===The thermodynamics of 'living'=== | ||
Biologists often view living things from the perspective of [[thermodynamics]] — the science of interactions among [[energy]] (the capacity to do work), [[heat]] (thermal energy), [[work]] (movement through force), [[entropy]] (degree of disorder) and [[information]] (degree of order). <ref>'''Note''': A random pattern of parts has no order (it has maximum entropy) | Biologists often view living things from the perspective of [[thermodynamics]] — the science of interactions among [[energy]] (the capacity to do work), [[heat]] (thermal energy), [[work]] (movement through force), [[entropy]] (degree of disorder) and [[information]] (degree of order).<ref>'''Note''': A random pattern of parts has no order (it has maximum entropy) and no information. A living system has ''order'' in its organized functions, has computationally-rich informational content, and low entropy.</ref> The sum total of these interactions define what a system can and cannot do when interconverting energy and work. For example, by the [[First Law of Thermodynamics]], when a process converts one form of energy to another, it results in no net loss of energy and no net gain.<ref>'''Note''': At birth, the Universe received a global energy account. The total energy of the Universe always remains constant, but if and when it completely disperses itself as heat into many little accounts, it has degraded to the point it can no longer do work. At that point the Universe has reached a state of absent energy gradients: a state of equilibrium characterized by complete randomness.</ref> | ||
Scientists discovered the laws of thermodynamics through experiment, debate, mathematical formulation and refinement; [[Albert Einstein]] believed that they stood as an edifice of physical theory that could never topple. | Scientists discovered the laws of thermodynamics through experiment, debate, mathematical formulation and refinement; [[Albert Einstein]] believed that they stood as an edifice of physical theory that could never topple. The [[Second Law of Thermodynamics]] may be most pertinent to an analysis of living systems: | ||
[[Image:Jpl_SUN.jpg|thumb|300px|right|Energy | [[Image:Jpl_SUN.jpg|thumb|300px|right|Energy emitted by our sun provides the great bulk of the energy gradient that living systems on earth exploit, either directly or indirectly, to maintain a state far from the equilibrium state of randomness. The photograph shows a handle-shaped cloud of plasma (hot ions) erupting from the Sun. Courtesy NASA/JPL-Caltech.[http://photojournal.jpl.nasa.gov/target/Sun?start=10] ]] | ||
:*Heat flows spontaneously — i.e., without external help — from a region of higher temperature to one of lower temperature, and never spontaneously in the reverse direction. That also holds for other forms of energy, including electromagnetic and chemical energy | :*Heat flows spontaneously — i.e., without external help — from a region of higher temperature to one of lower temperature, and never spontaneously in the reverse direction. That also holds for other forms of energy, including electromagnetic and chemical energy: concentrations of energy disperse to lower energy levels, flowing "into the cool",<ref name=schneider05> Schneider ED, Sagan D (2005) ''Into the Cool: Energy Flow, Thermodynamics, and Life.'' Chicago: The University of Chicago Press. ISBN 0-226-73937-6 [http://www.intothecool.com/ Chapter Excerpts and Reviews]</ref> so to speak. | ||
:*When heat as input to a system causes it to perform work (e.g., in a steam engine), some heat always dissipates as ‘exhaust’, unused and unusable by the system for further work. That also holds for other forms of energy doing work; some of the energy always turns into | :*When heat as input to a system causes it to perform work (e.g., in a steam engine), some heat always dissipates as ‘exhaust’, unused and unusable by the system for further work. That also holds for other forms of energy doing work; some of the energy always turns into exhaust, typically heat. Energy conversion to work in a system can never proceed at 100% efficiency. | ||
:*The degree of order or organization of a system and its surroundings | :*Consequences arise from the fact that work can produce organization in a system, but only by exporting disorganizing heat to its surroundings. Experiments reveal the ‘organizational balance’. The degree of order or organization of a system and its surroundings never increases when energy produces work. Scientists have learned how to put a number on the degree of disorder of a system, or system and surrounds, and they refer to it as [[entropy]].<ref>'''Note''': Unless contrived to do work, heat has a disordering, entropy-increasing effect. The more heat put into a system at a given temperature, the greater the entropy. At lower temperatures, the same heat input can increase entropy more, because the greater degree of order present at lower temperatures means a greater fractional increase in disorder.</ref> Water vapor, with its molecules distributed nearly randomly, has a higher entropy than liquid water, with its molecules distributed less randomly, and a much higher entropy than ice, with its molecules distributed in a more organized crystal array. Left to itself, ice tends to spontaneously melt and liquid water to evaporate. Order tends to disorder, with the Universe as a whole tending to exhaust itself into an ‘equilibrium’ state of randomness. | ||
Those three expressions of the Second Law reflect the fact that energy and order spontaneously flow downhill — down a ‘gradient’ — toward eliminating the gradient, as if nature abhors gradients of energy and order.<ref name=schneider05/> Upon gradient elimination, all energy and order has dissipated, all change ceases, and an equilibrium state ensues. Given this, how do living entities manage to come into existence, to develop from an | Those three expressions of the Second Law reflect the fact that energy and order spontaneously flow downhill — down a ‘gradient’ — toward eliminating the gradient, as if nature abhors gradients of energy and order.<ref name=schneider05/> Upon gradient elimination, all energy and order has dissipated, all change ceases, and an equilibrium state ensues. Given this, how do living entities manage to come into existence, to develop from an embryonic state to one of greater order and lesser entropy, and to perpetuate their order and increase in order? How do they thwart the Second Law? | ||
They don’t: they only seem to do so. Actually, they exploit the Universe’s gradients of energy and order | They don’t: they only seem to do so. Actually, they exploit the Universe’s gradients of energy and order, which run 'downhill'. Like a steam engine, they import energy and order, convert it, albeit incompletely, to the work of internal organization, and so reduce their internal entropy. But all along they emit enough 'exhaust' to increase the disorder and entropy of their surroundings, so that the total entropy of the living system ''and'' its surroundings increase, in keeping with the Second Law. | ||
Biological cells qualify as ''non-equilibrium thermodynamic systems'' because they consume energy to live, and because they export unusable (degraded) energy to dissipate the energy gradient they find themselves in — in keeping with the Second Law. Living things can store energy and perform work both on themselves and their environment; only after a living thing dies do all parts relate to each other according to ''spontaneous'' physical and chemical processes. When alive, a living system always performs its organized functional activities far from the 'equilibrium' state of activity that would ensue if no energy could be imported: energy from outside supplies the driving force that keeps the system far from equilibrium. ''Non-equilibrium thermodynamic systems'', including living things, can exhibit unexpectedly complex behaviors when maintained far | Biological cells qualify as ''non-equilibrium thermodynamic systems'' because they consume energy to live, and because they export unusable (degraded) energy to dissipate the energy gradient they find themselves in — in keeping with the Second Law. Living things can store energy and perform work both on themselves and their environment; only after a living thing dies do all parts relate to each other according to ''spontaneous'' physical and chemical processes. When alive, a living system always performs its organized functional activities far from the 'equilibrium' state of activity that would ensue if no energy could be imported: energy from outside supplies the driving force that keeps the system far from equilibrium. ''Non-equilibrium thermodynamic systems'', including living things, can exhibit unexpectedly complex behaviors when maintained far from equilibrium, and one very remarkable behavior that can result from this disequilibrum is [[self-organization]].<ref name=prigogine97>Prigogine I, Stengers I (1997) ''The End of Certainty: Time, Chaos, and the New Laws of Nature.'' Free Press, New York. ISBN 0684837056</ref> | ||
Moreover, some biophysicists propose that the production of order in an energy gradient, as occurs in living things, tends to develop ''inevitably'' and to proceed ''inexorably''. | Moreover, some biophysicists propose that the production of order in an energy gradient, as occurs in living things, tends to develop ''inevitably'' and to proceed ''inexorably''. They give two reasons: (1) the production of order, by exporting more than counterbalancing disorder, increases total entropy production (i.e., dissipates the energy gradient and renders the dissipated energy unusable) beyond that which would otherwise occur, and (2) energy sources dissipate their gradient to produce disorder at the fastest rate possible — to reach equilibrium as fast as they can. In other words, the physical principles governing energy gradient dissipation and energy degradation not only ''allows'' the development of living systems, but, in effect, tends to ''select'' for them, in particular, when no constraints are present disallowing their development (e.g., excess heat, poverty of appropriate chemicals).<ref name=swenson91&97>Swenson R, Turvey MT (1991) Thermodynamic reasons for perception-action cycles. Ecol Psychol [http://www.ecologicalpsychology.com/index.html 3:317-48]. Swenson R (1997) [http://www.entropylaw.com/thermoevolution1.html Thermodynamics, Evolution, and Behavior.] In ''The Encyclopedia of Comparative Psychology'' G. Greenberg and M. Haraway (Eds), New York: Garland Publishers, Inc. </ref> Thermodynamic principles thus may contribute not only to answering the question “what is life?” but also to “why is there life?”.<ref name=schneiderkay94>Schneider ED, Kay JJ (1994) Life as a manifestation of the second law of thermodynamics. Math Computer Modelling [http://www.nesh.ca/jameskay/www.fes.uwaterloo.ca/u/jjkay/pubs/Life_as/text.html 19:25-48]</ref> | ||
We can, then, view a living system as a state of organizational activity maintained by importing, storing and transforming energy and matter into the work and structures needed to sustain that state. They can only do so by producing waste and exporting it, and this lowers the organizational state of the environment. A living system maintains its organization at the expense of its external environment, leaving the environment more disorganized than the gain in organization of the living system — in keeping with the Second Law of | We can, then, view a living system as a state of organizational activity maintained by importing, storing and transforming energy and matter into the work and structures needed to sustain that state. They can only do so by producing waste and exporting it, and this lowers the organizational state of the environment. A living system maintains its organization at the expense of its external environment, leaving the environment more disorganized than the gain in organization of the living system — in keeping with the Second Law of Thermodynamics. Thus, from a thermodynamic perspective: | ||
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<span class="plainlinks">[http://darwin-online.org.uk/content/frameset?itemID=F373&viewtype=side&pageseq=1 Full-Text Here]</span> | <span class="plainlinks">[http://darwin-online.org.uk/content/frameset?itemID=F373&viewtype=side&pageseq=1 Full-Text Here]</span> | ||
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Historically, fires and storms have | Historically, fires and storms both have achieved status as living entities in human imagination. Although some non-living entities, such as tornadoes or the flames of candles, exist, like living things, as non-equilibrium open thermodynamic systems, they lack essential qualities of living things, and those deficiencies remove scientific credence of the 'poetic' view. Tornadoes and candle flames cannot 'reproduce' themselves, as cells and organisms can. Fire may spread and tornadoes may split, but the full system that comprises each phenomenon does not self-replicate. Living systems not only have open access to the environment in terms of energy and entropy exchange, but '''also''' have ''the capability of reproducing themselves.'' When a living system reproduces itself, its offspring inherit its properties, but with variations introduced by random events (including mutations). Some variations offer some of the offspring<ref>'''Note''': ....or the progeny of some conspecific living systems. Many living systems coexist with similar living systems, constituting a 'species', or group of 'conspecifics'.</ref> less opportunity to reproduce than others, and other offspring better opportunity, sometimes better even than their parents. Accordingly, new groups with different properties arise that may supplant older groups because of their greater reproductive fitness. Biologists call this "[[evolution]] by [[natural selection]]", and regard it as the most important way whereby living systems evolve over geological time.<ref name=jablonka05>Jablonka E, Lamb MJ (2005) ''Evolution in Four Dimension: Genetic, Epigenetic, Behavioral, and Symbolic Variation in the History of Life.'' Cambridge: The MIT Press</ref> | ||
Therefore, biologists recognize the ability to produce offspring that inherit some of its features, but with some variation due to chance, as an essential characteristic of living systems. They refer to it as | Therefore, biologists recognize the ability to produce offspring that inherit some of its features, but with some variation due to chance, as an essential characteristic of living systems. They refer to it as ''descent with modification''.<ref>Darwin C (1982; originally 1859) ''The Origin of Species By Means of Natural Selection or the Preservation of Favoured Races in the Struggle for Life.'' London: Penguin Books ISBN 9780140432053</ref> [[Evolution]] by natural selection will occur if heritable variations produce offspring that differ in their reproductive fitness. The variations occur due to chance variations in the inherited genetic recipe ([[genotype]]) for constructing the organismic traits (phenotype). In all living systems, [[DNA]] primarily provides the genetic recipe. All living things extant today descended with modification from an ancient ancestral community of microorganisms. To glimpse beyond that horizon, we will need to take heed of the findings of intense current research on early cellular evolution.<ref>See [[Evolution of cells]]</ref> | ||
[[Virus|Viruses]] have few of the characteristics of living systems described above, but they do have a [[genotype]] and phenotype, making them subject to natural selection and evolution. Accordingly, descent with modification is not uniquely a characteristic of living systems. Beyond the scope of this article, we find descent with modification in [[memes]] and the [[artificial life]] of [[software|computer software]], such as self-modifying [[computer viruses]] and programs created through genetic programming. Descent with modification has also been proposed to account for the evolution of the universe.<ref>Smolin L (1997) ''The Life of the Cosmos.'' New York: Oxford University Press. ISBN 019510837X</ref> | [[Virus|Viruses]] have few of the characteristics of living systems described above, but they do have a [[genotype]] and phenotype, making them subject to natural selection and evolution. Accordingly, descent with modification is not uniquely a characteristic of living systems. Beyond the scope of this article, we find descent with modification in [[memes]] and the [[artificial life]] of [[software|computer software]], such as self-modifying [[computer viruses]] and programs created through genetic programming. Descent with modification has also been proposed to account for the evolution of the universe.<ref>Smolin L (1997) ''The Life of the Cosmos.'' New York: Oxford University Press. ISBN 019510837X</ref> | ||
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===The exobiologists' view=== | ===The exobiologists' view=== | ||
[[Exobiology|Exobiologists]] (also known as | [[Exobiology|Exobiologists]] (also known as astrobiologists) consider issues relating to the possible existence of extraterrestrial living systems. Dirk Schulze-Makuch and Louis Irwin attempted to distill the essential characteristics of a living system in their book ''Life in the Universe.''<ref>Schulze-Makuch D, Irwin LN, Definition of Life. In ''Life in the Universe.'' Berlin: Springer-Verlag 2004: Chapter 2. pp 8-34 [http://dx.doi.org/10.1007/10825622_2 Link to Summary and Full-Text]</ref> They stress these characteristics, which resonate with the systems, thermodynamic and evolutionary perspectives discussed above: | ||
:*a microenvironment, with a boundary between it and its external environment, | :*a microenvironment, with a boundary between it and its external environment, | ||
:*the ability of that microenvironment to transform energy and matter from the environment to maintain a highly ordered, 'organizational' state (a low entropy state), | :*the ability of that microenvironment to transform energy and matter from the environment to maintain a highly ordered, 'organizational' state (a low entropy state), | ||
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===Self-organization=== | ===Self-organization=== | ||
Self-organization emerges from the interaction of life's components. In cells, self-organization emerges in part from the chemical properties of the proteins that are encoded in their genes.<ref name=lehn02>Lehn JM (2002) Toward self-organization and complex matter. Science 295:[http://dx.doi.org/10.1126/science.1071063 2400-3]</ref> Those proteins make their appearance through a genetic transcription-translation machinery, which represents a self-organized molecular machine that itself emerges in part from the chemical properties of proteins and other molecules.<ref>'''Note''': The qualifier "in part" reflects the need to invoke not only molecular self-assembly but also evolutionary mechanisms selecting genes that yield proteins whose chemical properties enable interactions that tend to optimize functional self-organization — in other words, adaption to circumstances. One must also invoke local real-time selective processes that confer stability and appropriate functionality to molecular self-assembly, called [[homeostasis]]. Self-organization and adaptation conjoin to yield function. | |||
:Heylighen F (2001) The Science of Self-organization and Adaptivity. In: Kiel LD (ed.) ''Knowledge Management, Organizational Intelligence and Learning, and Complexity: The Encyclopedia of Life Support Systems'' [http://pcp.vub.ac.be/Papers/PapersFH2.html (EOLSS)] Oxford: Eolss </ref> Molecules interact by forming and breaking strong covalent bonds, and also through weaker, quasi-stable non-covalent electromagnetic interactions, like hydrogen bonding and [[van der Waals' forces]]. Those interactions give aggregates of molecules the physical properties that underlie many biological processes.<ref name=lehn02/><ref>Reinhoudt DN, Crego-Calama M (2002) Synthesis beyond the molecule. Science 295:[http://dx.doi.org/10.1126/science.1069197 2403-7] | :*Heylighen F (2001) The Science of Self-organization and Adaptivity. In: Kiel LD (ed.) ''Knowledge Management, Organizational Intelligence and Learning, and Complexity: The Encyclopedia of Life Support Systems'' [http://pcp.vub.ac.be/Papers/PapersFH2.html (EOLSS)] Oxford: Eolss </ref> Molecules interact by forming and breaking strong covalent bonds, and also through weaker, quasi-stable non-covalent electromagnetic interactions, like hydrogen bonding and [[van der Waals' forces]]. Those interactions give aggregates of molecules the physical properties that underlie many biological processes.<ref name=lehn02/><ref>Reinhoudt DN, Crego-Calama M (2002) Synthesis beyond the molecule. Science 295:[http://dx.doi.org/10.1126/science.1069197 2403-7]. Percec V ''et al.'' (2006) CHEMISTRY: Self-assembly in action. Science [http://dx.doi.org/10.1126/science.1129512 313:2403-7]</ref> | ||
One way to understand self-organization is to view the genetic information (the ''genome'') as a 'computer program' that guides construction of the components of the cell that then arrange themselves according to their chemical properties. That arrangement, with the tinkering comprising local trial-and-error and evolution’s handiwork, can then carry out ('compute') integrative functions that are not explicitly encoded in the genome.<ref name=noble02>Noble D (2002) Modeling the heart—from genes to cells to the whole organ. Science 295:[http://dx.doi.org/10.1126/science.1069881 1678-82]</ref> The | One way to understand self-organization is to view the genetic information (the ''genome'') as a 'computer program' that guides construction of the components of the cell that then arrange themselves according to their chemical properties. That arrangement, with the tinkering comprising local trial-and-error and evolution’s handiwork, can then carry out ('compute') integrative functions that are not explicitly encoded in the genome.<ref name=noble02>Noble D (2002) Modeling the heart—from genes to cells to the whole organ. Science 295:[http://dx.doi.org/10.1126/science.1069881 1678-82]</ref> The molecular biologist [[Sidney Brenner]]<ref>Sidney Brenner’s Nobel lecture (2002) [http://nobelprize.org/nobel_prizes/medicine/laureates/2002/brenner-lecture.html “Nature’s Gift to Science”]</ref> expressed the metaphor this way: | ||
<blockquote>"...biological systems can be viewed as special computing devices. This view emerges from considerations of how information is stored in and retrieved from the genes. Genes can only specify the properties of the proteins they code for, and any integrative properties of the system must be 'computed' by their interactions. This provides a framework for analysis by simulation and sets practical bounds on what can be achieved by reductionist models.”<ref>Brenner S (1998) Biological computation. Novartis Found Symp 213:106-11 PMID 9653718</ref></blockquote> | <blockquote>"...biological systems can be viewed as special computing devices. This view emerges from considerations of how information is stored in and retrieved from the genes. Genes can only specify the properties of the proteins they code for, and any integrative properties of the system must be 'computed' by their interactions. This provides a framework for analysis by simulation and sets practical bounds on what can be achieved by reductionist models.”<ref>Brenner S (1998) Biological computation. Novartis Found Symp 213:106-11 PMID 9653718</ref></blockquote> | ||
The patterns of structure and behavior in self-organized systems need no behind-the-scene 'master', and no prepared recipes that specify the structure and dynamics of the system. Instead, | The patterns of structure and behavior in self-organized systems need no behind-the-scene 'master controller', and no prepared recipes that specify the structure and dynamics of the system. Instead, those patterns emerge from the interactions among the naturally selected components of a system, dictated by their physical properties, and dynamically modified by the emerging organization, which is itself modified by the environment. Thus the single-celled zygote self-organizes into a multicellular living system as the genetically encoded proteins interact, responding to changing influences from the changing environment generated by growing multicellularity — becoming a network of many cell-types working cooperatively. That biological systems self-organize has led one prominent biologist to say they are products of a "blind watchmaker".<ref>Dawkins R (1988) ''The Blind Watchmaker: Why the Evidence of Evolution Reveals a Universe Without Design.'' New York: W.W. Norton & Company, Inc. ISBN 0393304485 Excerpt from Amazon.com review: “The title of this 1986 work, Dawkins's second book, refers to the Rev. William Paley's 1802 work, ''Natural Theology'', which argued that, just as finding a watch would lead you to conclude that a watchmaker must exist, the complexity of living organisms proves that a Creator exists. Not so, says Dawkins: "the only watchmaker in nature is the blind forces of physics, albeit deployed in a very special way... it is the blind watchmaker." Physics, of course, includes open-system non-equilibrium thermodynamics.</ref> | ||
Self-organization tends to breed greater self-organization | Self-organization tends to breed greater complexity of self-organization. One important aspect of self-organization in cells rests on the tendency for lipids with polar (water-loving) and non-polar (water-shunning) ends to line up side-by-side to form bilayers in an aqueous solution, each unit of the bilayer with two lipid non-polar ends mutually attracted in the center and the polar ends surrounded by water. Membranes thereby form. Proteins can span the bilayer membrane, or selectively straddle only one or the other side of the membrane and its aqueous surrounding, according to their specific amino-acid sequence and side-groups. Other aspects of self-organization: Genes express not only proteins that organize themselves into a functional unit, but also proteins that organize themselves to regulate that unit, as in transcription regulatory circuits. Protein networks interact in a self-organizing way to produce networks of networks with complex levels of coordination, as in metabolic pathways. Cells communicate with other cells, either in free-living cellular communities or in multicellular organisms, and those communication activities self-organize by virtue of the properties of the cells, selected for fitness by evolutionary mechanisms, and subject to downward effects by the systems' organization and environmental influences on the systems. | ||
Further elaborating the descriptions of living systems beyond the thermodynamic and evolutionary perspectives, we might say that: | Further elaborating the descriptions of living systems beyond the thermodynamic and evolutionary perspectives, we might say that: | ||
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[[Image:Fetus_leonardo.jpg|thumb|350px|left|Views of a Foetus in the Womb (c. 1510 - 1512) is a drawing by Leonardo da Vinci. Detail. Although this near term fetus is a symbol of a new human life, the drawing is of a cadaver specimen. | [[Image:Fetus_leonardo.jpg|thumb|350px|left|Views of a Foetus in the Womb (c. 1510 - 1512) is a drawing by Leonardo da Vinci. Detail. Although this near term fetus is a symbol of a new human life, the drawing is of a cadaver specimen. | ||
[http://www.drawingsofleonardo.]]] | [http://www.drawingsofleonardo.]]] | ||
Stuart Kauffman uses the concept of 'autonomous agents' to explain living systems.<ref name=kauffman03>Kauffman S (2003) Molecular autonomous agents. Philos Transact A Math Phys Eng Sci. 361:1089-99 PMI: 12816601</ref> <ref>Kauffman SA (2000) ''Investigations.'' Oxford University Press, Oxford. ISBN 019512104X [http://www.oup.com/us/catalog/general/subject/LifeSciences/EvolutionaryBiology/?view=usa&ci=9780195121056 Publisher’s description and reviews]</ref> He gives the hypothetical example of an enzyme that catalyzes the binding of two smaller sub-component molecules into a copy of itself — self-replication by | Stuart Kauffman uses the concept of 'autonomous agents' to explain living systems.<ref name=kauffman03>Kauffman S (2003) Molecular autonomous agents. Philos Transact A Math Phys Eng Sci. 361:1089-99 PMI: 12816601</ref><ref>Kauffman SA (2000) ''Investigations.'' Oxford University Press, Oxford. ISBN 019512104X [http://www.oup.com/us/catalog/general/subject/LifeSciences/EvolutionaryBiology/?view=usa&ci=9780195121056 Publisher’s description and reviews]</ref> He gives the hypothetical example of an enzyme that catalyzes the binding of two smaller sub-component molecules into a copy of itself — self-replication by auto-catalysis. The energy to produce the enzyme comes from a neighboring molecule, by breaking an energy-rich bond, thus the neighbor molecule serves as a 'motor' to produce excess enzyme. The self-replication stops after using all duplicates of the motor, so to sustain self-replication, external energy — perhaps from light impinging on the system — must drive the repair of the broken chemical bond, re-establishing an ample supply of that energy-supplying molecule, thereby re-energizing the motor. A new cycle of auto-catalytic self-replication can then begin, given an ample influx of both external energy and 'food' (sub-components of the auto-catalytic enzyme). As an essential feature, interactions among the components of a system have effects (technically '[[allosteric]]' effects) that help organize and coordinate its processes, allowing the self-replication to proceed.<ref name=kauffman03/> | ||
Kauffman conceives, then, of an autocatalytic molecule in a network of molecules that has cycles of self-replication driven by external energy and materials. The network has a self-replication process as a subsystem, and a | Kauffman conceives, then, of an autocatalytic molecule in a network of molecules that has cycles of self-replication driven by external energy and materials. The network has a self-replication process as a subsystem, and a motor, namely, the breakup of an energy-rich molecule, supplying energy that drives the self-replication, and its re-energizing repair by transduction of external energy. Such a network is a 'molecular autonomous agent' because, given external energy (e.g., photons) and ample materials (the molecules needed to assemble the autocatalytic enzyme), the network perpetuates its existence;. The network is ''autonomous'' because it is not controlled by outside forces even though it depends on outside energy and materials. The 'agent' is the system doing work autonomously; in this case, the work of auto-catalytic self-replication. (That's what 'agents' do; they do work.) In this example, the agent survives by ‘eating’ outside materials and energy. Work gets done because the system remains far-from-equilibrium: as energy flows through the system, the system does its work, and in so doing dissipates the energy gradient, but it temporarily constrains the rate of dissipation by storing energy in its internal organization. The agent continues to live (survive and self-replicate) only while that far-from-equilibrium state exists, and it can be starved to 'death' by stopping the matter and energy from flowing through the system. Kauffman argues that cells, and indeed all living systems, qualify as autonomous agents, constructed from ''molecular'' autonomous agents.<ref name=kauffman03/> | ||
Autonomous agents also interest scientists in the fields of artificial intelligence and artificial life. One careful description of autonomous agents from some members of that group adds further insight to | Autonomous agents also interest scientists in the fields of artificial intelligence and artificial life. One careful description of autonomous agents from some members of that group adds further insight to this view of living systems: | ||
<blockquote> | <blockquote> | ||
"An autonomous agent is a system situated within and a part of an environment that senses that environment and acts on it, over time, in pursuit of its own agenda and so as to effect what it senses in the future. It has the properties of reactivity (timely response to environmental changes; autonomy (controls its own actions); goal-orientation (pursues its own agenda); continuous processing. Some autonomous agents may also have the properties of communicability (with other agents); adaptability (based on previous experience); unscripted flexibility." <ref>Franklin S, Graesser A (1996) [http://www.cs.memphis.edu/~franklin/AgentProg.html Is it an Agent, or just a Program?: A Taxonomy for Autonomous Agents.] Proc Third Int Workshop on Agent Theories, Architectures, and Languages, Springer-Verlag</ref> | "An autonomous agent is a system situated within and a part of an environment that senses that environment and acts on it, over time, in pursuit of its own agenda and so as to effect what it senses in the future. It has the properties of reactivity (timely response to environmental changes; autonomy (controls its own actions); goal-orientation (pursues its own agenda); continuous processing. Some autonomous agents may also have the properties of communicability (with other agents); adaptability (based on previous experience); unscripted flexibility."<ref>Franklin S, Graesser A (1996) [http://www.cs.memphis.edu/~franklin/AgentProg.html Is it an Agent, or just a Program?: A Taxonomy for Autonomous Agents.] Proc Third Int Workshop on Agent Theories, Architectures, and Languages, Springer-Verlag</ref> | ||
</blockquote> | </blockquote> | ||
For Kauffman, the property of pursuing its own agenda includes contributing to its own survival and reproduction: "...an autonomous agent is something that can both reproduce itself and do at least one thermodynamic work cycle. It turns out that this is true of all free-living cells, excepting weird special cases. They all do work cycles, just like the bacterium spinning its flagellum as it swims up the glucose gradient. The cells in your body are busy doing work cycles all the time." <ref>Kauffman S (2003) [http://www.edge.org/3rd_culture/kauffman03/kauffman_index.html ''The Adjacent Possible'']</ref> There is only one escape from work, and that is death. | For Kauffman, the property of pursuing its own agenda includes contributing to its own survival and reproduction: "...an autonomous agent is something that can both reproduce itself and do at least one thermodynamic work cycle. It turns out that this is true of all free-living cells, excepting weird special cases. They all do work cycles, just like the bacterium spinning its flagellum as it swims up the glucose gradient. The cells in your body are busy doing work cycles all the time."<ref>Kauffman S (2003) [http://www.edge.org/3rd_culture/kauffman03/kauffman_index.html ''The Adjacent Possible'']</ref> There is only one escape from work, and that is death. | ||
If the descriptions of living systems from thermodynamic, evolutionary, self-organizational and autonomous agent perspectives are considered, we might say that: | If the descriptions of living systems from thermodynamic, evolutionary, self-organizational and autonomous agent perspectives are considered, we might say that: | ||
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[[Image:Yeast_transcription_reg_modules.png|thumb|450px|right|The modular organization of a cellular network. Yeast Transcriptional Regulatory Modules. Nodes represent modules, and boxes around the modules represent module groups. Directed edges represent regulatory relationship. The functional categories of the modules are color-coded. (Reproduced from Bar-Joseph Z ''et al.'' (2003) Computational discovery of gene modules and regulatory networks. Nat Biotechnol 21:1337–42) From: Qi Y, Ge H Modularity and dynamics of cellular networks. PLoS Comp Biol 2(12):[http://dx.doi.org/10.1371/journal.pcbi.0020174 e174] ]] | [[Image:Yeast_transcription_reg_modules.png|thumb|450px|right|The modular organization of a cellular network. Yeast Transcriptional Regulatory Modules. Nodes represent modules, and boxes around the modules represent module groups. Directed edges represent regulatory relationship. The functional categories of the modules are color-coded. (Reproduced from Bar-Joseph Z ''et al.'' (2003) Computational discovery of gene modules and regulatory networks. Nat Biotechnol 21:1337–42) From: Qi Y, Ge H Modularity and dynamics of cellular networks. PLoS Comp Biol 2(12):[http://dx.doi.org/10.1371/journal.pcbi.0020174 e174] ]] | ||
The science of networks<ref name=Barabasi02>Barabási AL (2002) ''Linked: The New Science of Networks.'' Cambridge, Mass: Perseus Pub. ISBN 0-7382-0667-9</ref> provides another useful perspective on living things. Networks ‘re-present’ a system as | The science of networks<ref name=Barabasi02>Barabási AL (2002) ''Linked: The New Science of Networks.'' Cambridge, Mass: Perseus Pub. ISBN 0-7382-0667-9</ref> provides another useful perspective on living things. Networks ‘re-present’ a system as 'nodes’ and ‘interactions’ among the nodes (also referred to as ‘edges’ or ‘arrows’ or ‘links’). For example, in a spoken sentence, words and phrases make up the nodes, and the interconnections of syntax (subject-to-predicate, preposition-to-object of preposition, etc.) make up the links. Intracellular molecular networks represent specific functions in the cell; molecules make up the nodes, and their interactions with other nodes make up the edges or arrows. Some networks accept inputs of one kind and return outputs of a different kind. | ||
One | One finds networks everywhere in biology, from intracellular signaling pathways, to intraspecies networks, to ecosystems. Humans deliberately construct social networks of individuals working (more or less) to a common purpose, such as the U.S. Congress; they also construct networks of electronic parts to produce, for example, mobile phones; and networks of sentences and paragraphs to express messages, including this very article. Researchers view the [[World Wide Web]] as a network, and study its characteristics and dynamics.<ref name=Barabasi02/><ref>Watts DJ. (2007) A twenty-first century science. Nature 2007;445:[http://dx.doi.org/10.1038/445489a 489]</ref> | ||
According to Alon, "The cell can be viewed as an overlay of at least three types of networks, which describes protein-protein, protein-DNA, and protein-metabolite interactions."<ref name=alon2003> Alon U (2003) Biological networks: the tinkerer as an engineer. Science 301: [http://dx.doi.org/10.1126/science.1089072 1866-7] PMID 14512615</ref> Alon notes that cellular networks are like many human engineered networks in that they show 'modularity', 'robustness', and 'motifs': | According to Alon, "The cell can be viewed as an overlay of at least three types of networks, which describes protein-protein, protein-DNA, and protein-metabolite interactions."<ref name=alon2003> Alon U (2003) Biological networks: the tinkerer as an engineer. Science 301: [http://dx.doi.org/10.1126/science.1089072 1866-7] PMID 14512615</ref> Alon notes that cellular networks are like many human engineered networks in that they show 'modularity', 'robustness', and 'motifs': | ||
<br> | <br> | ||
:*Modules are | :* ''Modules'' are subnetworks with a specific function and which connect with other modules often only at one input node and one output node. Modularity facilitates adaptation to a changing environment, as, to produce an adaptation, evolution need tinker with just a few modules rather than with the whole system. Evolution can sometimes 'exapt' existing modules for new functions that contribute to reproductive fitness. For example, the swim bladder evolved as an adaptation for control of buoyancy but was exapted as a respiratory organ in various groups of fish.<ref>[http://www.palaeos.com/Vertebrates/Lists/Glossary/GlossaryEo.html See definition]</ref> | ||
:*Robustness describes how a network is able to | :* ''Robustness'' describes how a network is able to maintain its functionality despite environmental perturbations that affect the components. Robustness also reduces the range of network types that researchers must consider, because only certain types of networks are robust. | ||
:*Network motifs offer economy of network design, as the same circuit can have many different uses in cellular regulation, as in the case of autoregulatory circuits and feedforward loops. Nature selects motifs in part for their ability to make networks robust, so systems use motifs that work well over and over again in many different networks. <ref name=alon07nat>Alon U (2007) Simplicity in biology. Nature 446:[http://dx.doi.org/10.1038/446497a 497]</ref> In several well-studied biological networks, the abundance of network motifs — small subnetworks — correlates with the degree of robustness.<ref>Prill RJ ''et al.'' (2004) Dynamic properties of network motifs contribute to biological network organization. PLoS Biol 3: [http://dx.doi.org/10.1371/journal.pbio.0030343 e343]</ref> Networks, like those in cells and those in neural networks in the brain,<ref>Sporns O, Kotter R (2004) Motifs in brain networks. PLoS Biol 2: [http://dx.doi.org/10.1371/journal.pbio.0020369 e369]</ref> use motifs as basic building blocks, like multicellular organisms use cells as basic building blocks. Motifs offer biologists a level of simplicity of biological functionality for their efforts to model the dynamics of organized hierarchies of networks.<ref name=alon07nat/> | :* ''Network motifs'' offer economy of network design, as the same circuit can have many different uses in cellular regulation, as in the case of autoregulatory circuits and feedforward loops. Nature selects motifs in part for their ability to make networks robust, so systems use motifs that work well over and over again in many different networks.<ref name=alon07nat>Alon U (2007) Simplicity in biology. Nature 446:[http://dx.doi.org/10.1038/446497a 497]</ref> In several well-studied biological networks, the abundance of network motifs — small subnetworks — correlates with the degree of robustness.<ref>Prill RJ ''et al.'' (2004) Dynamic properties of network motifs contribute to biological network organization. PLoS Biol 3: [http://dx.doi.org/10.1371/journal.pbio.0030343 e343]</ref> Networks, like those in cells and those in neural networks in the brain,<ref>Sporns O, Kotter R (2004) Motifs in brain networks. PLoS Biol 2: [http://dx.doi.org/10.1371/journal.pbio.0020369 e369]</ref> use motifs as basic building blocks, like multicellular organisms use cells as basic building blocks. Motifs offer biologists a level of simplicity of biological functionality for their efforts to model the dynamics of organized hierarchies of networks.<ref name=alon07nat/> | ||
The view of the cell as an overlay of mathematically-definable dynamic networks can reveal how a living system can exist as an improbable, intricate, self-orchestrated dance of molecules. <ref>Alon U (2007) ''An Introduction to Systems Biology: Design Principles of Biological Circuits.'' Boca Raton: Chapman and Hall/CRC</ref> | The view of the cell as an overlay of mathematically-definable dynamic networks can reveal how a living system can exist as an improbable, intricate, self-orchestrated dance of molecules.<ref>Alon U (2007) ''An Introduction to Systems Biology: Design Principles of Biological Circuits.'' Boca Raton: Chapman and Hall/CRC</ref> The 'overlay of networks' view also suggests how the concept of self-organized networks can extend to all higher levels of living systems. | ||
Further elaborating the descriptions of living systems beyond the thermodynamic, evolutionary, | Further elaborating the descriptions of living systems beyond the thermodynamic, evolutionary, self-organizational and autonomous agent perspectives we might say that: | ||
{|cellpadding=10 align=center style="width: | {|cellpadding=10 align=center style="width:70%; border: solid 1px #4682b4; background:lightblue" | ||
|A living system has the ability to remain for a time in a near steady-state as a self-organized system of '''hierarchical robust modular networks'''. It works autonomously to offset responses to perturbations | |A living system has the ability to remain for a time in a near steady-state as a self-organized system of '''hierarchical robust modular networks'''. It works autonomously to offset responses to perturbations and to reproduce itself, enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. Finally, it is capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. | ||
|} | |} | ||
===Information processing=== | ===Information processing=== | ||
Bioscientists study biological systems for many different reasons, hence biology has many subdisciplines (see [[Biology]] and [[List of biology topics]]). But in every subdiscipline, bioscientists study biological systems for the proximate reason of gaining information about the system to satisfy their however-motivated curiosity | Bioscientists study biological systems for many different reasons, hence biology has many subdisciplines (see [[Biology]] and [[List of biology topics]]). But in every subdiscipline, bioscientists study biological systems for the proximate reason of gaining information about the system to satisfy their however-motivated curiosity and to apply that information to human agendas (e.g., to prevent disease or to conserve the environment). Those realities attest that biological systems harbor information, at least as people usually understand the term. To appreciate how this perspective can contribute to understanding living systems, the following questions need answers: | ||
:*what do we mean by information? | :*what do we mean by information? | ||
:*how does information apply to biological systems? | :*how does information apply to biological systems? | ||
:*how does information emerge in biological systems? | :*how does information emerge in biological systems? | ||
:*how do the answers to those questions add to explaining living systems? | :*how do the answers to those questions add to explaining living systems? | ||
The word 'information' comes from the verb 'to inform', originally meaning to put form in something: the seal in-forms the wax, and the wax now contains in-formation. A random collection of particles or other entities has no form, nothing has given it form, and it contains no in-formation. The more randomness in the structure of the collection, the fewer improbable arrangements or interactions it has among its parts.[[Image:DNA_to_living_system2.jpg|thumb|400px|left|Information processing from DNA to a living system. Genes are made up of DNA, and contain the information used by other cellular components to create proteins. A cell is tightly packed with tens of thousands of proteins and other molecules, often working as multimolecular | The word 'information' comes from the verb 'to inform', originally meaning to put form in something: the seal in-forms the wax, and the wax now contains in-formation. A random collection of particles or other entities has no form, nothing has given it form, and it contains no in-formation. The more randomness in the structure of the collection, the fewer improbable arrangements or interactions it has among its parts.[[Image:DNA_to_living_system2.jpg|thumb|400px|left|Information processing from DNA to a living system. Genes are made up of DNA, and contain the information used by other cellular components to create proteins. A cell is tightly packed with tens of thousands of proteins and other molecules, often working as multimolecular 'machines' to perform essential cellular activities. Courtesy U.S. Department of Energy. http://DOEgenomestolife.org/pubs/overview.pdf or http://genomicsgtl.energy.gov/pubs/overview_screen.pdf]]<br> | ||
A drinking glass falls onto the sidewalk, it falls apart into a random collection of bits of glass. Notice it doesn’t regroup into the drinking glass — you could watch it for a lifetime. Our experience shows us that the drinking glass is more improbable than the glass in smithereens. The more ''improbable'' the arrangements, the more ''in-formation'' a collection of parts has received and therefore contains. An observer will conclude that something has happened to | A drinking glass falls onto the sidewalk, it falls apart into a random collection of bits of glass. Notice it doesn’t regroup into the drinking glass — you could watch it for a lifetime. Our experience shows us that the drinking glass is more improbable than the glass in smithereens. The more ''improbable'' the arrangements, the more ''in-formation'' a collection of parts has received and therefore contains. An observer will conclude that something has happened to form the parts into a more improbable state — an in-formation has occurred, and that the collection of parts contains that in-formation. By that reasoning, biological systems<ref>'''Note''': This article takes the view that cells underlie ‘living systems’, and that cellular subsystems, like transcription networks and metabolic pathways, qualify as ‘biological systems’ but not as ‘living systems’.</ref> contain in-formation: something has happened to 'form' the parts into an improbable state. | ||
An ordered desktop soon becomes disordered. The ordered desktop has message value, or 'information', in that something must have happened to give it form. The more unlikely the arrangement of the parts, the more information it contains. Biological systems have information content in that they are unlikely (non-random) arrangements of parts, non-random collections of interactions of parts, non-random collections of functional activities. | An ordered desktop soon becomes disordered. The ordered desktop has message value, or 'information', in that something must have happened to give it form. The more unlikely the arrangement of the parts, the more information it contains. Biological systems have information content in that they are unlikely (non-random) arrangements of parts, non-random collections of interactions of parts, and non-random collections of functional activities. | ||
The thermodynamic and autonomous agent perspectives discussed cells as intermediates in a gradient of higher to lower forms of usable energy. The flow of energy through the cell feeds it, enabling it to work to gain ''form'', or order, and to gain functionalities, raising its information content.<ref>'''Note''': That does ''not'' explain the ''origin'' of the ability to utilize available energy and materials. To explain ''that'' requires knowledge of the origin of living systems. See [[Origin of life]]</ref> The cell can do work on its environment also. | The thermodynamic and autonomous agent perspectives discussed cells as intermediates in a gradient of higher to lower forms of usable energy. The flow of energy through the cell feeds it, enabling it to work to gain ''form'', or order, and to gain functionalities, raising its information content.<ref>'''Note''': That does ''not'' explain the ''origin'' of the ability to utilize available energy and materials. To explain ''that'' requires knowledge of the origin of living systems. See [[Origin of life]]</ref> The cell can do work on its environment also. | ||
Thus a living system emerges as an information processing system. It can receive information from energy<ref>'''Note''': Usable energy, also called ‘free energy’, in virtue of its organized state that flows downhill to dissipated uselessness, has all the attributes of information.</ref> and materials in its environment, fueling and supplying the machinery that builds and sustains information-rich organization; it can generate new information inside itself, as in embryonic development; and it can transmit information within and outside itself, as in transcription regulation and exporting [[pheromones]]. From its parent, it inherits information that establishes its developmental potential and scripts its realization | Thus a living system emerges as an information processing system. It can receive information from energy<ref>'''Note''': Usable energy, also called ‘free energy’, in virtue of its organized state that flows downhill to dissipated uselessness, has all the attributes of information.</ref> and materials in its environment, fueling and supplying the machinery that builds and sustains information-rich organization; it can generate new information inside itself, as in embryonic development; and it can transmit information within and outside itself, as in transcription regulation and exporting [[pheromones]]. From its parent, it inherits information that establishes its developmental potential and scripts its realization — including information that enables it to reproduce itself. | ||
Combined with other perspectives, viewing living systems as information banks, as inheritors, receivers, generators and transmitters of information, and as reproducers of inherited information, enables one to see living systems and their interactions with other living systems as a vast, complex, naturally-selected, self-sustaining, evolving communication network. Recently (on the timescale of evolving living systems) that evolving communication network emerged as the human brain, capable of communicating with itself and other humans using networks of symbols.<ref>Deacon TW (1997) ''The Symbolic Species: The Co-Evolution of Language and the Brain.'' New York: W.W. Norton & Company, Inc. ISBN 0393038386 </ref> That led to the emergence of cultural evolution, a whole new domain of self-reproducing entities ('culturgens', 'memes') and descent with modification. That in turn led to the emergence of another vast communication network: books, [[wiki|wikis]], and other technologies of information generation and exchange. | |||
We might now consider another closely related perspective, a ‘cognitive’ perspective.<ref>Danchin A ''et al.'' (2007) The extant core bacterial proteome is an archive of the origin of life. Proteomics [http://dx.doi.org/10.1002/pmic.200600442 7:875–89]</ref> Given that networks resist common perturbations (e.g., by their robustness, and by ‘homeostasis’), one might think of them as containing a representation of their environment and of how it might vary. As networks self-organize through interactions between proteins, any network 'representation’ of its environment must derive from the genetic information that determines those proteins. The genetic information comprises a molecular code, and the process that transforms that information into proteins describes an algorithm — the transcription-translation algorithm. As these algorithms evolved through natural selection, one can view evolution as selecting for cognitive functionality in the genome — the ability to ‘represent’ the cell’s environment and, more generally, to remember and anticipate. | |||
The genetic information has the form of a digital code, one whose execution jump-starts cellular processes, including the processes that lead to self-organization of networks that regulate execution of the genetic digital code — the gene regulatory networks. A separate digital code also has a central role in the operation of those gene regulatory networks: the code adjacent to a gene determines which transcription regulating factors can bind there, and thereby controls gene activity. In other words, a digital code, separate from the code that specifies the proteins of the gene regulatory networks, gives specificity to the behavior of those networks and to their regulation of the execution of the genetic digital code.<ref name=hoodage03>Hood L (2003) Systems biology: integrating technology, biology, and computation. Mechanisms of Ageing and Development [http://dx.do.org/10.1016/S0047-6374(02)00164-1 124:9-16]</ref> Eventually, digital codes surrender to decipherment, offering the hope that we might someday read the message of living and find ways to edit it. | |||
Further elaborating beyond the thermodynamic, evolutionary, self-organizational, autonomous agent | Further elaborating beyond the thermodynamic, evolutionary, self-organizational, autonomous agent and network perspectives we might say that: | ||
{|cellpadding=10 align=center style="width:80%; border: solid 1px #4682b4; background:lightblue" | {|cellpadding=10 align=center style="width:80%; border: solid 1px #4682b4; background:lightblue" | ||
|A living system has the '''informational content and information-processing faculty''' to remain for a time in a near steady-state as a self-organized system of hierarchical robust modular networks. It works autonomously to offset responses to perturbations | |A living system has the '''informational content and information-processing faculty''' to remain for a time in a near steady-state as a self-organized system of hierarchical robust modular networks. It works autonomously to offset responses to perturbations and to reproduce itself, enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. Finally, it is capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. | ||
|} | |} | ||
==Organic chemistry as informatics== | ==Organic chemistry as informatics== | ||
Why the central place of [[carbon]] in the chemistry of all earth’s living things? The [[Physical chemistry|physical chemistry]] of carbon allows it to bond with many other elements, especially hydrogen, oxygen, nitrogen and phosphorus, and, even to form carbon-to-carbon bonds. The avidity for carbon to bond to itself allows carbon atoms to easily join into long chains and closed rings; and allows small organic molecules (such as [[sugar]]s, [[amino acid]]s and [[nucleotide]]s) to | Why the central place of [[carbon]] in the chemistry of all earth’s living things? The [[Physical chemistry|physical chemistry]] of carbon allows it to bond with many other elements, especially hydrogen, oxygen, nitrogen and phosphorus, and, even to form carbon-to-carbon bonds. The avidity for carbon to bond to itself allows carbon atoms to easily join into long chains and closed rings; and allows small organic molecules (such as [[sugar]]s, [[amino acid]]s and [[nucleotide]]s) to join into huge [[macromolecule]]s that are remarkably stable at standard conditions. These macromolecules are the repositories of information used by living entities. | ||
The variety of carbon bonds vary in strength as well as in 3-D conformation; adding a dynamic quality to many organic molecules. The simplest set of bonds that carbon can form is that of a tetrahedron, or pyramid. Other types of bonds involve more than one shared electron, and for that reason are called double, and triple bonds; importantly, these different bonds constitute three entirely different geometries. Changing from one type of carbon-to-carbon bond to another type, as when a double bond is reduced to a single bond, will cause energy changes but without destroying the molecule. Such changes not only affect free energy, but also affect the actual shape of the molecule and the particular side groups attached to it. In this way, for at least some organic molecules, the 'pulse of life' is represented at an atomic level. | The variety of carbon bonds vary in strength as well as in 3-D conformation; adding a dynamic quality to many organic molecules. The simplest set of bonds that carbon can form is that of a tetrahedron, or pyramid. Other types of bonds involve more than one shared electron, and for that reason are called double, and triple bonds; importantly, these different bonds constitute three entirely different geometries. Changing from one type of carbon-to-carbon bond to another type, as when a double bond is reduced to a single bond, will cause energy changes but without destroying the molecule. Such changes not only affect free energy, but also affect the actual shape of the molecule and the particular side groups attached to it. In this way, for at least some organic molecules, the 'pulse of life' is represented at an atomic level. | ||
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These properties of carbon mean that organic macromolecules are capable of containing tremendous 'banks' of information coded in their very structure. Not only can each of the constituent molecules be huge, but several categories of chemicals, like [[nucleotide]]s or [[amino acid]]s, that contain several different species, can be ordered so that the possible combinations are effectively limitless. All of these molecules are involved in the molecular-interaction networks of cells. Amogst these networks of interactions are those that enable cells to import and transform energy and energy-rich matter from the environment and that ultimately enable cells to grow, survive and reproduce. | These properties of carbon mean that organic macromolecules are capable of containing tremendous 'banks' of information coded in their very structure. Not only can each of the constituent molecules be huge, but several categories of chemicals, like [[nucleotide]]s or [[amino acid]]s, that contain several different species, can be ordered so that the possible combinations are effectively limitless. All of these molecules are involved in the molecular-interaction networks of cells. Amogst these networks of interactions are those that enable cells to import and transform energy and energy-rich matter from the environment and that ultimately enable cells to grow, survive and reproduce. | ||
Elsewhere in the universe, where conditions differ greatly from earth’s, other | Elsewhere in the universe, where conditions differ greatly from earth’s, other elements may hold a central place in life. Silicon, carbon's close relative on the [[The Periodic Table of Elements|periodic table]], also forms bonds with itself, but they have little stability under conditions compatible with life as we know it. In places in the universe where physical conditions might favor silicon-based macromolecules, silicon-based life might exist.<ref name=bains04>Bains W (2004) Many chemistries could be used to build living systems. Astrobiology PMID 15253836 [http://www.liebertonline.com/doi/abs/10.1089%2F153110704323175124 4:137-67]</ref> | ||
==Identifying the different scientific perspectives on life== | ==Identifying the different scientific perspectives on life== | ||
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:*The basic building blocks of all living systems are ''cells''; the basic (genetic) information that generates cells comes as part of their starting materials. This information, in the form of nucleic acid macromolecules, encodes many different types of proteins that interact to assemble an organization that can import energy and export waste. Cells inherit this information from ‘parent’ cells, raising two as yet unanswered questions: ''how did cells arise in the first place?'' and ''how did they acquire stores of information?'';<ref>'''Note''': We can arrive at a more-or-less empirically sound explanation of what constitutes living systems without having a good explanation for how they arose in the first place, because we can study the here-and-now and not the there-and-then.</ref> (see [[Origin of life]] and [[Evolution of cells]]) | :*The basic building blocks of all living systems are ''cells''; the basic (genetic) information that generates cells comes as part of their starting materials. This information, in the form of nucleic acid macromolecules, encodes many different types of proteins that interact to assemble an organization that can import energy and export waste. Cells inherit this information from ‘parent’ cells, raising two as yet unanswered questions: ''how did cells arise in the first place?'' and ''how did they acquire stores of information?'';<ref>'''Note''': We can arrive at a more-or-less empirically sound explanation of what constitutes living systems without having a good explanation for how they arose in the first place, because we can study the here-and-now and not the there-and-then.</ref> (see [[Origin of life]] and [[Evolution of cells]]) | ||
:*The molecular interactions are governed by the universal laws of physics and chemistry; those laws, together with the inherited information, enable a self-organizing system that can work autonomously for survival and reproduction, and allow properties to emerge that could not be anticipated from those of the system's components alone. | :*The molecular interactions are governed by the universal laws of physics and chemistry; those laws, together with the inherited information, enable a self-organizing system that can work autonomously for survival and reproduction, and allow properties to emerge that could not be anticipated from those of the system's components alone. | ||
:*The activities of a living system | :*The activities of a living system have no 'master controller'; they need only a type of organization that maintains the system far-from-equilibrium, which can yield improbable self-organized structures and activities. | ||
:*Living things cannot escape from changing external conditions, so they must exhibit robustness in their organization and must be adaptable to maintain their stability. Robustness and adaptability derive from the properties of a hierarchical network of subnetworks of molecular circuits; | :*Living things cannot escape from changing external conditions, so they must exhibit robustness in their organization and must be adaptable to maintain their stability. Robustness and adaptability derive from the properties of a hierarchical network of subnetworks of molecular circuits; | ||
:*Living systems must produce enough reproductive variability to allow evolution through natural selection, which guides the continuation of a 3.5 billion year history of Earth’s | :*Living systems must produce enough reproductive variability to allow evolution through natural selection, which guides the continuation of a 3.5 billion year history of Earth’s living world. By evolution, living systems generate increasing varieties of living systems, occupy an extreme spectrum of environments, create their own environments,<ref>Odling-Smee FJ, Laland KN, Feldman MW (2003) ''Niche Construction; The Neglected Process in Evolution.'' Princeton: Princeton University Press. ISBN 0691044384</ref> and permit sufficient complexity to enable them to process information in a way that allows them to ‘experience’ themselves. | ||
==Synthesis of perspectives on what constitutes Life== | ==Synthesis of perspectives on what constitutes Life== | ||
The activity of living, for a cell-based system, depends on the ability to maintain a near steady-state of organized functioning far from the state of randomness. The system achieves that in part because of its location in the path of a downhill gradient of flowing energy. It exploits that gradient through its abilities to import some of the energy flowing past it | The activity of living, for a cell-based system, depends on the ability to maintain a near steady-state of organized functioning far from the state of randomness. The system achieves that in part because of its location in the path of a downhill gradient of flowing energy. It exploits that gradient through its abilities to import some of the energy flowing past it and to export unusable energy and material, thus increasing its own order at the expense of a more than counterbalancing disorder of its surroundings. | ||
Those principles seem to apply to all living systems: single cells, multicellular organs and organisms, and multi-organism demes and ecosystems. | Those principles seem to apply to all living systems: single cells, multicellular organs and organisms, and multi-organism demes and ecosystems. | ||
The building block of all living systems is the cell. For cells to utilize available external energy | The building block and working unit of all living systems is the cell. For cells to utilize available external energy or energy-rich matter and achieve order, they must have, from the outset, some informational content. That enables the cell to produce components that can, by molecular interactions, respond to the imported energy and material to organize themselves. That organization comprises modular networks of molecular interactions, and networks of interacting networks — self-organized and coordinated functional interactions. The properties of the networks and those of the hierarchy of networks enable the system to perpetuate itself, and to maintain its steady-state despite fluctuations in environmental factors. That principle, too, applies to all living systems. Any organism, plant or animal, comprises a network of organs working autonomously, maintaining its steady-state functioning far from equilibrium in response to environmental perturbations — physiologists refer to that as ''[[homeostasis]]''. | ||
The networks that regulate the flow of information through the cell were 'designed' by natural selection and other evolutionary processes. That is, | The networks that regulate the flow of information through the cell were 'designed' by natural selection and other evolutionary processes. That is, the codes that evolved by natural selection were those which produced molecules that could interact in ways that contribute to self-organization of those networks that enable a cell to sustain and reproduce itself. The collaboration of natural selection and physico-chemical laws perpetuates living systems not only in real-time but also in geological, or ‘evolutionary’, time. From common ancestors — however they may have arisen (see [[Evolution of cells]]) — informationally-guided, self-organizing, autonomous network dynamics enabled generation of the diversity of all living systems on the planet, over a period of more than three billion years. Living systems perpetuate living systems, exploiting free energy on its inexorable path to dissipation and degradation, and harvesting energy in developing systems organization by a more than counterbalancing dis-organizing of the larger system in which it is embedded. | ||
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====Further reading==== | ====Further reading==== | ||
:'''Books''' | :'''Books''' | ||
*Schrodinger E (1944-2000) | *Schrodinger E (1944-2000) ''What is Life?'' Cambridge University Press (Canto). ISBN 0-521-42708-8 [http://dieoff.org/page150.htm Chapter 6: Order, Disorder and Entropy] ''(Prediction of hereditary molecule like a coded periodic crystal — Watson claims inspiration — Stresses open thermodynamic systems key to life.)'' | ||
*Kaneko K (2006) | *Kaneko K (2006) ''Life: An Introduction to Complex Systems Biology.'' Springer, Berlin ISBN 3-540-32666-9 | ||
*Dill KA, Bromberg S, Stigter D (2003) | *Dill KA, Bromberg S, Stigter D (2003) ''Molecular Driving Forces: Statistical Thermodynamics in Chemistry and Biology.'' Garland Science, New York. ISBN 0-8153-2051-5 | ||
*Strogatz SH (2003) | *Strogatz SH (2003) ''Sync: The Emerging Science of Spontaneous Order.'' Theia, New York ISBN 0-7868-6844-9 | ||
*Buchanan M (2002) | *Buchanan M (2002) ''Nexus: Small Worlds and the Groundbreaking Science of Networks.'' W.W. Norton, New York ISBN 0-393-04153-0 | ||
*Hoagland M, Dodson B, Hauck J (2001) | *Hoagland M, Dodson B, Hauck J (2001) ''Exploring the Way Life Works: The Science of Biology.'' Jones and Bartlett Publishers, Inc, Mississauga, Ontario ISBN 0-7637-1688-X ''(For young people. An illustrated text.)'' | ||
*Solé R, Goodwin B (2000) | *Solé R, Goodwin B (2000) ''Signs of Life: How Complexity Pervades Biology.'' Basic Books, Perseus Books Group, New York ISBN 0-465-01928-5 | ||
*Loewenstein WR (2000) | *Loewenstein WR (2000) ''The Touchstone of life: Molecular Information, Cell Communication, and the Foundations of Life.'' Oxford University Press ISBN 0-19-514057-5 [http://www.nytimes.com/books/first/l/loewenstein-life.html Book Review and Chapter One] | ||
*Hoagland M, Dodson B (1998) | *Hoagland M, Dodson B (1998) ''The Way Life Works: The Science Lovers Illustrated Guide to How Life Grows, Develops, Reproduces, and Gets Along.'' Three Rivers Press, New York ISBN 0-8129-2888-1 ''(For young people. An illustrated text.)'' | ||
*Margulis L, Sagan D (1995) | *Margulis L, Sagan D (1995) ''What is Life?'' Simon & Schuster ISBN 0-684-81087-5 | ||
:'''Articles''' | :'''Articles''' | ||
*Epstein IR, Pojman JA, Steinbock O | *Epstein IR, Pojman JA, Steinbock O (2006) Introduction: Self-organization in nonequilibrium chemical systems. Chaos 16:037101 PMID 17014235 | ||
*Hazen R | *Hazen R (2006) The Big Questions: What is Life? ''New Scientist'' Issue 2578, [http://space.newscientist.com/article/mg19225780.071;jsessionid=LMABLDFPFNJN/ 46-51] | ||
*Marenduzzo D ''et al.'' (2006) Entropy-driven genome organization. Biophys J 90:3712- | *Marenduzzo D ''et al.'' (2006) Entropy-driven genome organization. Biophys J 90:3712-21 PMID 16500976 | ||
*Morowitz H, Smith E (2006) | *Morowitz H, Smith E (2006) [http://www.santafe.edu/research/publications/workingpapers/06-08-029.pdf Energy flow and the organization of life] | ||
*Scheffer M, van Nes EH (2006) Self-organized similarity, the evolutionary emergence of groups of similar species. Proc Natl Acad Sci USA 103:6230- | *Scheffer M, van Nes EH (2006) Self-organized similarity, the evolutionary emergence of groups of similar species. Proc Natl Acad Sci USA 103:6230-5 PMID 16585519 | ||
*Walsh DM (2006) Organisms as natural purposes: The contemporary evolutionary perspective. Studies in History and Philosophy of Science. Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37:771- | *Walsh DM (2006) Organisms as natural purposes: The contemporary evolutionary perspective. Studies in History and Philosophy of Science. Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37:771-91 [http://dx.do.org/doi:10.1016/j.shpsc.2006.09.009 37:771-91] | ||
*Park K | *Park K ''et al.'' (2005) Self-organized scale-free networks. Phys Rev E Stat Nonlin Soft Matter Phys 72:026131 PMID 16196668 | ||
*Troisi A | *Troisi A ''et al.''(2005) An agent-based approach for modeling molecular self-organization. Proc Natl Acad Sci USA 102:255-60 PMID 15625108 | ||
*Pace NR | *Pace NR (2001) Special Feature: The universal nature of biochemistry. Proc Natl Acad Sci USA 98:[http://www.pnas.org/cgi/content/full/98/3/805/ 805-8]<br> | ||
*Dronamraju KR | *Dronamraju KR (1999) Erwin Schrodinger and the origins of molecular biology. [http://www.genetics.org Genetics] 153:1071-6 PMID 10545442 | ||
:'''Interviews and Commentaries''' | :'''Interviews and Commentaries''' | ||
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===Other characteristics shared by all living things=== | ===Other characteristics shared by all living things=== | ||
Living things share some very specific features not always explicitly stated above. For example, | Living things share some very specific features not always explicitly stated above. For example, | ||
* | *some evidence supports the proposition that all extant living things descended from a common ancestor <ref>Kurland CG, Collins LJ, Penny D (2006) Genomics and the irreducible nature of eukaryote cells. Science 312: [http://dx.doi.org/10.1126/science.1121674 1011-14]</ref> Other evidence suggests that "Extant life on Earth is descended not from one, but from three distinctly different cell types. However, the designs of the three have developed and matured, in a communal fashion, along with those of many other designs that along the way became extinct." <ref>Woese CR (2002) On the evolution of cells. Proc Natl Acad Sci U S A [http://dx.doi.org/10.1073pnas.132266999 99:8742-7] PMID 12077305 </ref> | ||
*only pre-existing cells can | *only pre-existing cells can 'manufacture' new cells; | ||
*only pre-existing multicellular organisms can | *only pre-existing multicellular organisms can manufacture new multicellular organisms; | ||
*a membrane encloses every cell, protecting each from dissolution into its external environment; | *a membrane encloses every cell, protecting each from dissolution into its external environment; | ||
:*the cell membrane contains molecular systems that enables the cell to import usable matter and energy and to export unusable matter and energy, and others that enable it to send and receive signals to and from other cells; | :*the cell membrane contains molecular systems that enables the cell to import usable matter and energy and to export unusable matter and energy, and others that enable it to send and receive signals to and from other cells; | ||
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==Appendix B== | ==Appendix B== | ||
=== Selected definitions of life === | === Selected definitions of life === | ||
Marcello Bárbieri, Professor of Morphology and Embryology at the University of Ferrara, Italy, collected an extensive list of definitions of “Life” from scientists and philosophers of the 19th and 20th centuries.<ref name=barbieri>Bárbieri M. (2003) | Marcello Bárbieri, Professor of Morphology and Embryology at the University of Ferrara, Italy, collected an extensive list of definitions of “Life” from scientists and philosophers of the 19th and 20th centuries.<ref name=barbieri>Bárbieri M. (2003) ''The Organic Codes; An Introduction to Semantic Biology.'' Cambridge: Cambridge University Press.</ref> Those selected below resonate with the systems and thermodynamic perspectives of living systems: | ||
*"The broadest and most complete definition of life will be "the continuous adjustment of internal to external relations". — | *"The broadest and most complete definition of life will be "the continuous adjustment of internal to external relations". — Herbert Spencer (1884) | ||
*"It is the particular manner of composition of the materials and processes, their spatial and temporal organisation which constitute what we call life." — A. Putter (1923) | *"It is the particular manner of composition of the materials and processes, their spatial and temporal organisation which constitute what we call life." — A. Putter (1923) | ||
*"A living organism is a system organised in a hierarchic order of many different parts, in which a great number of processes are so disposed that by means of their mutual relations, within wide limits with constant change of the materials and energies constituting the system, and also in spite of disturbances conditioned by external influences, the system ts generated or remains in the state characteristic of it, or these processes lead to the production of similar systems." — | *"A living organism is a system organised in a hierarchic order of many different parts, in which a great number of processes are so disposed that by means of their mutual relations, within wide limits with constant change of the materials and energies constituting the system, and also in spite of disturbances conditioned by external influences, the system ts generated or remains in the state characteristic of it, or these processes lead to the production of similar systems." — L. von Bertalanffy (1933) | ||
*"Life seems to be an orderly and lawful behaviour of matter, not based exclusively on its tendency to go from order to disorder, but based partly on existing order that is kept up." — | *"Life seems to be an orderly and lawful behaviour of matter, not based exclusively on its tendency to go from order to disorder, but based partly on existing order that is kept up." — E. Schrodinger (1944) | ||
*"Life is made of three basic elements: matter, energy and information. Any element in life that is not matter and energy can be reduced to information." — P.Fong (1973) | *"Life is made of three basic elements: matter, energy and information. Any element in life that is not matter and energy can be reduced to information." — P. Fong (1973) | ||
*"A living system is an open system that is self-replicating, self-regulating, and feeds on energy from the environment." — R. Sattler (1986) | *"A living system is an open system that is self-replicating, self-regulating, and feeds on energy from the environment." — R. Sattler (1986) | ||
'''Published collections of definitions of 'Life' ''' | '''Published collections of definitions of 'Life' ''' | ||
*Popa R (2004) [http://www.springerlink.com/content/28gdjrbc9nebykxy/?p=197c38ab3c344c79a1ea0dac8363c5f4&pi=10/ Chronology of Definitions and Interpretations of Life.] In: Popa R | *Popa R (2004) [http://www.springerlink.com/content/28gdjrbc9nebykxy/?p=197c38ab3c344c79a1ea0dac8363c5f4&pi=10/ Chronology of Definitions and Interpretations of Life.] In: Popa R (ed.) ''Between Necessity and Probability: Searching for the Definition and Origin of Life.'' Berlin: Springer-Verlag 2004: pp 197-205 ''(Quotes and source-citations from 1885 to 2002)'' | ||
*Barbieri M (2003) Appendix: Definitions of Life. In: | *Barbieri M (2003) Appendix: Definitions of Life. In: ''The Organic Codes: An Introduction to Semantic Biology.'' Cambridge, UK: Cambridge University Press ISBN 0521824141 ''(Quotes from 1802 to 2002) | ||
===The gray zone=== | ===The gray zone=== | ||
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</div> | </div> | ||
<br> | <br> | ||
[[Category:Biology]] | [[Category:Biology]] | ||
[[Category:CZ Live]] | [[Category:CZ Live]] | ||
[[Category:Biology Workgroup]] | [[Category:Biology Workgroup]] |
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What is life? Biologists use the word 'life' for both the processes of living, and for the things that carry out those processes. Life, too, connotes the relationships among living things, past and present: it includes the entire living world — the biosphere — and the whole history of 'life on earth'. In theory, life might include entities, now unknown, that exist on other planets. Just what qualities would such beings have to possess for scientists to acknowledge them as alive? Could non-living things ever acquire those same qualities? What features separated the first living cells from the inanimate materials that formed them? The answers to such questions form part of the larger answer to that most basic of all questions in Biology: "what is life?" This article focuses not on 'life', the noun, but on 'living', the verb; on what activities living entities perform, and on the processes that enable their performance.[1] It takes, as its theme, “Life is what is common to all living beings” (Christian De Duve).[2]
(see also Biology and Systems biology).
Principles of life
Molecules
- See related topics: Chemistry, Biochemistry, and Organic Chemistry
All known life is built from the same set of organic molecules. Although they contain many elements, organic molecules always have a predominant structure of carbon linked to itself. In living things, organic species exist in mixtures of colloidal aqueous solutions that are never completely homogeneous but are bounded by lipid and protein sheets. Each pool can have a different composition with distinct properties of charge, density, viscosity and osmotic pressure; these differences provide the basis for the generation of electric fields, fluid shifts, and transport of molecules. The stuff of life, then, is carbon chains, studded with other atoms, and arranged in lagoons of fat, water, and salts.
Cells
- See Related Topics: Cell Biology, Microbiology
As well as sharing a common carbon- and water-based chemistry, every entity that biologists acknowledge as living — bacteria, trees, fish, chimpanzees — shares a common building block, the cell. Cells are universally enclosed in a membrane (a phospholipid bilayer known as the cytoplasmic membrane), that separates the inside of the cell from the external environment. Interestingly, the chemistry of the cell membrane is not universal. In most types of cells the molecules of the membrane are based on esters of glycerol combined with straight chain fatty acids, but in the Archaea the chemistry of membranes is based on glycerol ether linkages and isoprene fatty components.
Many organisms live as isolated single cells, others form cooperative colonies of cells, and still other cells are members of complex multicellular systems that include diverse cell types, each specialized for different functions.[4] Nature has produced an enormous variety of cell types that span three vast ‘domains’ of living systems: Archaea, Bacteria, and Eukarya,[5] yet cells in all three domains have many features in common. All cells have a surrounding membrane; a physical boundary that separates them from their environment. The surface of that membrane always has special properties that allow protection, excretion, ingestion or communication. Often, these functions are provided by changes in the shape or actual chemical species present on the surface — so pores, receptor molecules and protective walls are often features of the cell surface. This is true in both unicellular and multicellular entities.[6]
Current evidence indicates that only pre-existing cells can ‘manufacture’ cells. So how did the first cell(s) arise?
Examining what all extant cells have in common may provide insight to the Origin of life. All extract chemical energy from simple oxidation reactions, and convert it into other, chemical forms of energy. The molecule ATP universally serves as the cell's main energy 'currency'. All cells inherit digitally stored information in the form of molecules of DNA, and with minor exceptions the DNA of all cells use the same universal genetic code to guide production of a myriad of distinct protein structures. Cells use those proteins to carry out diverse activities, including energy processing and conversion of carbon, nitrogen and phosphorous-containing materials into cellular structures. In the human genome, perhaps as few as 22,000 different protein-coding genes[7] lead to the production of perhaps more than a million distinct protein structures that make up the variety and quantity of protein molecules needed for the structures and functions of a cell. Numerous molecular mechanisms account for that quantitative gene-to-protein amplification.[8]
Nature has produced a huge diversity of single-celled organisms and large, complex animals or plants. The latter can contain vast numbers of cells, each part of a specialized subpopulation (cell types) — in a mammal, the cells that make up bone differ from those that make up muscle, and differ again from those that make up skin, for example. Humans contain approximately 200 different cell types as classified by microscopic anatomy.[9] In multicellular organisms, cells combine to make organs, the functional and structural components of the single larger organism.
So what makes a single celled organism 'alive', and does the answer apply also when we call a large complex multicellular animal or plant 'alive'? What exactly do we mean by 'living'?
Systems view of 'living'
(See main article, Systems biology)
The evolutionary biologist Ernst Mayr suggested that, to define 'life', we need to clarify what we mean by the process of 'living':
"The problem here is that 'life' suggests some 'thing' — a substance or force — and for centuries philosophers and biologists have tried to identify this 'vital force', to no avail. In reality, the noun 'life' is merely a reification of the process of living. It does not exist as an independent entity. One can deal with the process of living scientifically, something one cannot do with the abstraction 'life'. One can describe, and even try to define, what living is and what a living organism is, and one can try to make a demarcation between living and nonliving. Indeed, one can even try to explain how living as a process can be the product of molecules that themselves are not living."
The systems perspective of 'living' recalls Aristotle's four components of causality,[10] [11] in that a living thing comprises:
- A list of organic and inorganic parts (molecules and ions; cells, organelles, organs and organisms) — Aristotle’s 'material' cause;
- How the parts relate to each other to form structures (e.g., networks), how they interact with each other (e.g., network dynamics), and how the structures interact with each other in a coordinated dynamic and hierarchical manner — Aristotle’s 'formal' (form-like) cause;
- How the parts and structures became dynamically coordinated (e.g., gene expression; self-organization; competition) — Aristotle’s 'efficient' (effect-producing) cause; and
- How the living system as-a-whole functions and behaves, and the properties that characterize it (e.g., reproduction; locomotion; cognition) — Aristotle’s 'final' cause
The analysis of all of those components together forms part of the new discipline of Systems Biology. Systems biologists study, among other things, the phenomenon of 'emergence', whereby properties, functions, and behaviors of living systems arise though not exhibited by any individual component of the system, and not predictable from complete understanding the components' behaviors alone considered in isolation from the system that embeds them. Every cellular system exhibits emergent behaviors. Emergent behaviors of living systems include such things as locomotion, sexual display, flocking, and conscious experiencing.
Why do not all of the properties of a system predictably result from the properties of its components? After all, the reductionist paradigm that dominated the Scientific method in the 20th century operated on the exactly opposite assumption. For one thing, the intrinsic properties of a system’s components themselves do not determine those of the whole system; rather, their 'organizational dynamics' does, and those dynamics include not only the interrelations among the components themselves, but also interactions among the many different organizational units in the system. [12] Secondly, the living system always operates in a context (its external environment, or surroundings), and that, in turn, always affects the properties of the system-as-a-whole. For example, nutrient gradients influence the direction a bacterium’s locomotion. The impact of environmental context affects the organization of the components within the system — a 'downward causation'. [13] For another example, environmental signals can activate or suppress a metabolic pathway, reorganizing cellular activity[14] One cannot simply take a living system apart and predict how it will behave.
Philosopher of science D.M. Walsh puts it this way: "The constituent parts and processes of a living thing are related to the organism as a whole by a kind of 'reciprocal causation'."[15] In other words, the organization of the components determine the behavior of the system, but that organization arises from more than the set of its internal components. How the whole system behaves as it interacts with its environment determines how those components organize themselves, and so novel properties of the system 'emerge' that characterize neither the environment nor that set of internal components. For example, the behavior of a human kidney cell depends not only on its cellular physiology, but also on all the properties of the organ (kidney) which constitutes its environment. The kidney's overall structure and function influence the cell’s structure and behavior (e.g., by physical confinement and by cell-to-cell signaling), which in turn influence the organization of its intracellular components. The kidney in turn responds to its environment, namely the individual body that it lives in, and that body responds to its environment, which includes such factors as the availability of particular food items, fresh water, and ambient temperature and humidity. Systems biologists regard emergent properties as arising from from a combination of bottom-up and top-down effects — Walsh's 'reciprocal causation'.
Other basic concepts that systems biologists consider crucial in explaining living systems as-a-whole include 'robustness', 'modularity', and 'networks' — all discussed in sections below. Quantitative modeling and simulation guided by experimental biological data provide the mainstay methodologies of systems biologists. (See Systems biology)
The thermodynamics of 'living'
Biologists often view living things from the perspective of thermodynamics — the science of interactions among energy (the capacity to do work), heat (thermal energy), work (movement through force), entropy (degree of disorder) and information (degree of order).[16] The sum total of these interactions define what a system can and cannot do when interconverting energy and work. For example, by the First Law of Thermodynamics, when a process converts one form of energy to another, it results in no net loss of energy and no net gain.[17]
Scientists discovered the laws of thermodynamics through experiment, debate, mathematical formulation and refinement; Albert Einstein believed that they stood as an edifice of physical theory that could never topple. The Second Law of Thermodynamics may be most pertinent to an analysis of living systems:
- Heat flows spontaneously — i.e., without external help — from a region of higher temperature to one of lower temperature, and never spontaneously in the reverse direction. That also holds for other forms of energy, including electromagnetic and chemical energy: concentrations of energy disperse to lower energy levels, flowing "into the cool",[18] so to speak.
- When heat as input to a system causes it to perform work (e.g., in a steam engine), some heat always dissipates as ‘exhaust’, unused and unusable by the system for further work. That also holds for other forms of energy doing work; some of the energy always turns into exhaust, typically heat. Energy conversion to work in a system can never proceed at 100% efficiency.
- Consequences arise from the fact that work can produce organization in a system, but only by exporting disorganizing heat to its surroundings. Experiments reveal the ‘organizational balance’. The degree of order or organization of a system and its surroundings never increases when energy produces work. Scientists have learned how to put a number on the degree of disorder of a system, or system and surrounds, and they refer to it as entropy.[19] Water vapor, with its molecules distributed nearly randomly, has a higher entropy than liquid water, with its molecules distributed less randomly, and a much higher entropy than ice, with its molecules distributed in a more organized crystal array. Left to itself, ice tends to spontaneously melt and liquid water to evaporate. Order tends to disorder, with the Universe as a whole tending to exhaust itself into an ‘equilibrium’ state of randomness.
Those three expressions of the Second Law reflect the fact that energy and order spontaneously flow downhill — down a ‘gradient’ — toward eliminating the gradient, as if nature abhors gradients of energy and order.[18] Upon gradient elimination, all energy and order has dissipated, all change ceases, and an equilibrium state ensues. Given this, how do living entities manage to come into existence, to develop from an embryonic state to one of greater order and lesser entropy, and to perpetuate their order and increase in order? How do they thwart the Second Law?
They don’t: they only seem to do so. Actually, they exploit the Universe’s gradients of energy and order, which run 'downhill'. Like a steam engine, they import energy and order, convert it, albeit incompletely, to the work of internal organization, and so reduce their internal entropy. But all along they emit enough 'exhaust' to increase the disorder and entropy of their surroundings, so that the total entropy of the living system and its surroundings increase, in keeping with the Second Law.
Biological cells qualify as non-equilibrium thermodynamic systems because they consume energy to live, and because they export unusable (degraded) energy to dissipate the energy gradient they find themselves in — in keeping with the Second Law. Living things can store energy and perform work both on themselves and their environment; only after a living thing dies do all parts relate to each other according to spontaneous physical and chemical processes. When alive, a living system always performs its organized functional activities far from the 'equilibrium' state of activity that would ensue if no energy could be imported: energy from outside supplies the driving force that keeps the system far from equilibrium. Non-equilibrium thermodynamic systems, including living things, can exhibit unexpectedly complex behaviors when maintained far from equilibrium, and one very remarkable behavior that can result from this disequilibrum is self-organization.[20]
Moreover, some biophysicists propose that the production of order in an energy gradient, as occurs in living things, tends to develop inevitably and to proceed inexorably. They give two reasons: (1) the production of order, by exporting more than counterbalancing disorder, increases total entropy production (i.e., dissipates the energy gradient and renders the dissipated energy unusable) beyond that which would otherwise occur, and (2) energy sources dissipate their gradient to produce disorder at the fastest rate possible — to reach equilibrium as fast as they can. In other words, the physical principles governing energy gradient dissipation and energy degradation not only allows the development of living systems, but, in effect, tends to select for them, in particular, when no constraints are present disallowing their development (e.g., excess heat, poverty of appropriate chemicals).[21] Thermodynamic principles thus may contribute not only to answering the question “what is life?” but also to “why is there life?”.[22]
We can, then, view a living system as a state of organizational activity maintained by importing, storing and transforming energy and matter into the work and structures needed to sustain that state. They can only do so by producing waste and exporting it, and this lowers the organizational state of the environment. A living system maintains its organization at the expense of its external environment, leaving the environment more disorganized than the gain in organization of the living system — in keeping with the Second Law of Thermodynamics. Thus, from a thermodynamic perspective:
A living system has the ability to remain for a time in a near steady-state as an organized system. The organization is made possible by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby allowing a far-from-equilibrium state to be maintained. |
Evolutionary aspects of 'living'
Last Paragraph of Charles Darwin’s Origin of Species (1859) "It is interesting to contemplate an entangled bank, clothed with many plants of many kinds, with birds singing on the bushes, with various insects flitting about, and with worms crawling through the damp earth, and to reflect that these elaborately constructed forms, so different from each other, and dependent on each other in so complex a manner, have all been produced by laws acting around us. These laws, taken in the largest sense, being Growth with Reproduction; Inheritance which is almost implied by reproduction; Variability from the indirect and direct action of the external conditions of life, and from use and disuse; a Ratio of Increase so high as to lead to a Struggle for Life, and as a consequence to Natural Selection, entailing Divergence of Character and the Extinction of less-improved forms. Thus, from the war of nature, from famine and death, the most exalted object which we are capable of conceiving, namely, the production of the higher animals, directly follows. There is grandeur in this view of life, with its several powers, having been originally breathed into a few forms or into one; and that, whilst this planet has gone cycling on according to the fixed law of gravity, from so simple a beginning endless forms most beautiful and most wonderful have been, and are being, evolved." |
Historically, fires and storms both have achieved status as living entities in human imagination. Although some non-living entities, such as tornadoes or the flames of candles, exist, like living things, as non-equilibrium open thermodynamic systems, they lack essential qualities of living things, and those deficiencies remove scientific credence of the 'poetic' view. Tornadoes and candle flames cannot 'reproduce' themselves, as cells and organisms can. Fire may spread and tornadoes may split, but the full system that comprises each phenomenon does not self-replicate. Living systems not only have open access to the environment in terms of energy and entropy exchange, but also have the capability of reproducing themselves. When a living system reproduces itself, its offspring inherit its properties, but with variations introduced by random events (including mutations). Some variations offer some of the offspring[23] less opportunity to reproduce than others, and other offspring better opportunity, sometimes better even than their parents. Accordingly, new groups with different properties arise that may supplant older groups because of their greater reproductive fitness. Biologists call this "evolution by natural selection", and regard it as the most important way whereby living systems evolve over geological time.[24]
Therefore, biologists recognize the ability to produce offspring that inherit some of its features, but with some variation due to chance, as an essential characteristic of living systems. They refer to it as descent with modification.[25] Evolution by natural selection will occur if heritable variations produce offspring that differ in their reproductive fitness. The variations occur due to chance variations in the inherited genetic recipe (genotype) for constructing the organismic traits (phenotype). In all living systems, DNA primarily provides the genetic recipe. All living things extant today descended with modification from an ancient ancestral community of microorganisms. To glimpse beyond that horizon, we will need to take heed of the findings of intense current research on early cellular evolution.[26]
Viruses have few of the characteristics of living systems described above, but they do have a genotype and phenotype, making them subject to natural selection and evolution. Accordingly, descent with modification is not uniquely a characteristic of living systems. Beyond the scope of this article, we find descent with modification in memes and the artificial life of computer software, such as self-modifying computer viruses and programs created through genetic programming. Descent with modification has also been proposed to account for the evolution of the universe.[27]
Combining the thermodynamic and evolutionary perspectives, we might say that:
A living system has the ability to remain for a time in a near steady-state as an organized system. The organization is made possible by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby allowing a far-from-equilibrium state to be maintained. A system is also capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. |
The exobiologists' view
Exobiologists (also known as astrobiologists) consider issues relating to the possible existence of extraterrestrial living systems. Dirk Schulze-Makuch and Louis Irwin attempted to distill the essential characteristics of a living system in their book Life in the Universe.[28] They stress these characteristics, which resonate with the systems, thermodynamic and evolutionary perspectives discussed above:
- a microenvironment, with a boundary between it and its external environment,
- the ability of that microenvironment to transform energy and matter from the environment to maintain a highly ordered, 'organizational' state (a low entropy state),
- therefore, the ability of that microenvironment to remain in thermodynamic disequilibrium with its environment,
- the ability of that microenvironment to encode and transmit information.
Self-organization
Self-organization emerges from the interaction of life's components. In cells, self-organization emerges in part from the chemical properties of the proteins that are encoded in their genes.[29] Those proteins make their appearance through a genetic transcription-translation machinery, which represents a self-organized molecular machine that itself emerges in part from the chemical properties of proteins and other molecules.[30] Molecules interact by forming and breaking strong covalent bonds, and also through weaker, quasi-stable non-covalent electromagnetic interactions, like hydrogen bonding and van der Waals' forces. Those interactions give aggregates of molecules the physical properties that underlie many biological processes.[29][31]
One way to understand self-organization is to view the genetic information (the genome) as a 'computer program' that guides construction of the components of the cell that then arrange themselves according to their chemical properties. That arrangement, with the tinkering comprising local trial-and-error and evolution’s handiwork, can then carry out ('compute') integrative functions that are not explicitly encoded in the genome.[32] The molecular biologist Sidney Brenner[33] expressed the metaphor this way:
"...biological systems can be viewed as special computing devices. This view emerges from considerations of how information is stored in and retrieved from the genes. Genes can only specify the properties of the proteins they code for, and any integrative properties of the system must be 'computed' by their interactions. This provides a framework for analysis by simulation and sets practical bounds on what can be achieved by reductionist models.”[34]
The patterns of structure and behavior in self-organized systems need no behind-the-scene 'master controller', and no prepared recipes that specify the structure and dynamics of the system. Instead, those patterns emerge from the interactions among the naturally selected components of a system, dictated by their physical properties, and dynamically modified by the emerging organization, which is itself modified by the environment. Thus the single-celled zygote self-organizes into a multicellular living system as the genetically encoded proteins interact, responding to changing influences from the changing environment generated by growing multicellularity — becoming a network of many cell-types working cooperatively. That biological systems self-organize has led one prominent biologist to say they are products of a "blind watchmaker".[35]
Self-organization tends to breed greater complexity of self-organization. One important aspect of self-organization in cells rests on the tendency for lipids with polar (water-loving) and non-polar (water-shunning) ends to line up side-by-side to form bilayers in an aqueous solution, each unit of the bilayer with two lipid non-polar ends mutually attracted in the center and the polar ends surrounded by water. Membranes thereby form. Proteins can span the bilayer membrane, or selectively straddle only one or the other side of the membrane and its aqueous surrounding, according to their specific amino-acid sequence and side-groups. Other aspects of self-organization: Genes express not only proteins that organize themselves into a functional unit, but also proteins that organize themselves to regulate that unit, as in transcription regulatory circuits. Protein networks interact in a self-organizing way to produce networks of networks with complex levels of coordination, as in metabolic pathways. Cells communicate with other cells, either in free-living cellular communities or in multicellular organisms, and those communication activities self-organize by virtue of the properties of the cells, selected for fitness by evolutionary mechanisms, and subject to downward effects by the systems' organization and environmental influences on the systems.
Further elaborating the descriptions of living systems beyond the thermodynamic and evolutionary perspectives, we might say that:
A living system has the ability to remain for a time in a near steady-state as a self-organized system. The organization is enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. A system is also capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. |
Autonomous agents
Stuart Kauffman uses the concept of 'autonomous agents' to explain living systems.[36][37] He gives the hypothetical example of an enzyme that catalyzes the binding of two smaller sub-component molecules into a copy of itself — self-replication by auto-catalysis. The energy to produce the enzyme comes from a neighboring molecule, by breaking an energy-rich bond, thus the neighbor molecule serves as a 'motor' to produce excess enzyme. The self-replication stops after using all duplicates of the motor, so to sustain self-replication, external energy — perhaps from light impinging on the system — must drive the repair of the broken chemical bond, re-establishing an ample supply of that energy-supplying molecule, thereby re-energizing the motor. A new cycle of auto-catalytic self-replication can then begin, given an ample influx of both external energy and 'food' (sub-components of the auto-catalytic enzyme). As an essential feature, interactions among the components of a system have effects (technically 'allosteric' effects) that help organize and coordinate its processes, allowing the self-replication to proceed.[36]
Kauffman conceives, then, of an autocatalytic molecule in a network of molecules that has cycles of self-replication driven by external energy and materials. The network has a self-replication process as a subsystem, and a motor, namely, the breakup of an energy-rich molecule, supplying energy that drives the self-replication, and its re-energizing repair by transduction of external energy. Such a network is a 'molecular autonomous agent' because, given external energy (e.g., photons) and ample materials (the molecules needed to assemble the autocatalytic enzyme), the network perpetuates its existence;. The network is autonomous because it is not controlled by outside forces even though it depends on outside energy and materials. The 'agent' is the system doing work autonomously; in this case, the work of auto-catalytic self-replication. (That's what 'agents' do; they do work.) In this example, the agent survives by ‘eating’ outside materials and energy. Work gets done because the system remains far-from-equilibrium: as energy flows through the system, the system does its work, and in so doing dissipates the energy gradient, but it temporarily constrains the rate of dissipation by storing energy in its internal organization. The agent continues to live (survive and self-replicate) only while that far-from-equilibrium state exists, and it can be starved to 'death' by stopping the matter and energy from flowing through the system. Kauffman argues that cells, and indeed all living systems, qualify as autonomous agents, constructed from molecular autonomous agents.[36]
Autonomous agents also interest scientists in the fields of artificial intelligence and artificial life. One careful description of autonomous agents from some members of that group adds further insight to this view of living systems:
"An autonomous agent is a system situated within and a part of an environment that senses that environment and acts on it, over time, in pursuit of its own agenda and so as to effect what it senses in the future. It has the properties of reactivity (timely response to environmental changes; autonomy (controls its own actions); goal-orientation (pursues its own agenda); continuous processing. Some autonomous agents may also have the properties of communicability (with other agents); adaptability (based on previous experience); unscripted flexibility."[38]
For Kauffman, the property of pursuing its own agenda includes contributing to its own survival and reproduction: "...an autonomous agent is something that can both reproduce itself and do at least one thermodynamic work cycle. It turns out that this is true of all free-living cells, excepting weird special cases. They all do work cycles, just like the bacterium spinning its flagellum as it swims up the glucose gradient. The cells in your body are busy doing work cycles all the time."[39] There is only one escape from work, and that is death.
If the descriptions of living systems from thermodynamic, evolutionary, self-organizational and autonomous agent perspectives are considered, we might say that:
A living system has the ability to remain for a time in a near steady-state as a self-organized system. It works autonomously to offset responses to perturbations, and to reproduce itself, enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. Finally, it is capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. |
Networks
The science of networks[40] provides another useful perspective on living things. Networks ‘re-present’ a system as 'nodes’ and ‘interactions’ among the nodes (also referred to as ‘edges’ or ‘arrows’ or ‘links’). For example, in a spoken sentence, words and phrases make up the nodes, and the interconnections of syntax (subject-to-predicate, preposition-to-object of preposition, etc.) make up the links. Intracellular molecular networks represent specific functions in the cell; molecules make up the nodes, and their interactions with other nodes make up the edges or arrows. Some networks accept inputs of one kind and return outputs of a different kind.
One finds networks everywhere in biology, from intracellular signaling pathways, to intraspecies networks, to ecosystems. Humans deliberately construct social networks of individuals working (more or less) to a common purpose, such as the U.S. Congress; they also construct networks of electronic parts to produce, for example, mobile phones; and networks of sentences and paragraphs to express messages, including this very article. Researchers view the World Wide Web as a network, and study its characteristics and dynamics.[40][41]
According to Alon, "The cell can be viewed as an overlay of at least three types of networks, which describes protein-protein, protein-DNA, and protein-metabolite interactions."[42] Alon notes that cellular networks are like many human engineered networks in that they show 'modularity', 'robustness', and 'motifs':
- Modules are subnetworks with a specific function and which connect with other modules often only at one input node and one output node. Modularity facilitates adaptation to a changing environment, as, to produce an adaptation, evolution need tinker with just a few modules rather than with the whole system. Evolution can sometimes 'exapt' existing modules for new functions that contribute to reproductive fitness. For example, the swim bladder evolved as an adaptation for control of buoyancy but was exapted as a respiratory organ in various groups of fish.[43]
- Robustness describes how a network is able to maintain its functionality despite environmental perturbations that affect the components. Robustness also reduces the range of network types that researchers must consider, because only certain types of networks are robust.
- Network motifs offer economy of network design, as the same circuit can have many different uses in cellular regulation, as in the case of autoregulatory circuits and feedforward loops. Nature selects motifs in part for their ability to make networks robust, so systems use motifs that work well over and over again in many different networks.[44] In several well-studied biological networks, the abundance of network motifs — small subnetworks — correlates with the degree of robustness.[45] Networks, like those in cells and those in neural networks in the brain,[46] use motifs as basic building blocks, like multicellular organisms use cells as basic building blocks. Motifs offer biologists a level of simplicity of biological functionality for their efforts to model the dynamics of organized hierarchies of networks.[44]
The view of the cell as an overlay of mathematically-definable dynamic networks can reveal how a living system can exist as an improbable, intricate, self-orchestrated dance of molecules.[47] The 'overlay of networks' view also suggests how the concept of self-organized networks can extend to all higher levels of living systems.
Further elaborating the descriptions of living systems beyond the thermodynamic, evolutionary, self-organizational and autonomous agent perspectives we might say that:
A living system has the ability to remain for a time in a near steady-state as a self-organized system of hierarchical robust modular networks. It works autonomously to offset responses to perturbations and to reproduce itself, enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. Finally, it is capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. |
Information processing
Bioscientists study biological systems for many different reasons, hence biology has many subdisciplines (see Biology and List of biology topics). But in every subdiscipline, bioscientists study biological systems for the proximate reason of gaining information about the system to satisfy their however-motivated curiosity and to apply that information to human agendas (e.g., to prevent disease or to conserve the environment). Those realities attest that biological systems harbor information, at least as people usually understand the term. To appreciate how this perspective can contribute to understanding living systems, the following questions need answers:
- what do we mean by information?
- how does information apply to biological systems?
- how does information emerge in biological systems?
- how do the answers to those questions add to explaining living systems?
A drinking glass falls onto the sidewalk, it falls apart into a random collection of bits of glass. Notice it doesn’t regroup into the drinking glass — you could watch it for a lifetime. Our experience shows us that the drinking glass is more improbable than the glass in smithereens. The more improbable the arrangements, the more in-formation a collection of parts has received and therefore contains. An observer will conclude that something has happened to form the parts into a more improbable state — an in-formation has occurred, and that the collection of parts contains that in-formation. By that reasoning, biological systems[48] contain in-formation: something has happened to 'form' the parts into an improbable state.
An ordered desktop soon becomes disordered. The ordered desktop has message value, or 'information', in that something must have happened to give it form. The more unlikely the arrangement of the parts, the more information it contains. Biological systems have information content in that they are unlikely (non-random) arrangements of parts, non-random collections of interactions of parts, and non-random collections of functional activities.
The thermodynamic and autonomous agent perspectives discussed cells as intermediates in a gradient of higher to lower forms of usable energy. The flow of energy through the cell feeds it, enabling it to work to gain form, or order, and to gain functionalities, raising its information content.[49] The cell can do work on its environment also.
Thus a living system emerges as an information processing system. It can receive information from energy[50] and materials in its environment, fueling and supplying the machinery that builds and sustains information-rich organization; it can generate new information inside itself, as in embryonic development; and it can transmit information within and outside itself, as in transcription regulation and exporting pheromones. From its parent, it inherits information that establishes its developmental potential and scripts its realization — including information that enables it to reproduce itself.
Combined with other perspectives, viewing living systems as information banks, as inheritors, receivers, generators and transmitters of information, and as reproducers of inherited information, enables one to see living systems and their interactions with other living systems as a vast, complex, naturally-selected, self-sustaining, evolving communication network. Recently (on the timescale of evolving living systems) that evolving communication network emerged as the human brain, capable of communicating with itself and other humans using networks of symbols.[51] That led to the emergence of cultural evolution, a whole new domain of self-reproducing entities ('culturgens', 'memes') and descent with modification. That in turn led to the emergence of another vast communication network: books, wikis, and other technologies of information generation and exchange.
We might now consider another closely related perspective, a ‘cognitive’ perspective.[52] Given that networks resist common perturbations (e.g., by their robustness, and by ‘homeostasis’), one might think of them as containing a representation of their environment and of how it might vary. As networks self-organize through interactions between proteins, any network 'representation’ of its environment must derive from the genetic information that determines those proteins. The genetic information comprises a molecular code, and the process that transforms that information into proteins describes an algorithm — the transcription-translation algorithm. As these algorithms evolved through natural selection, one can view evolution as selecting for cognitive functionality in the genome — the ability to ‘represent’ the cell’s environment and, more generally, to remember and anticipate.
The genetic information has the form of a digital code, one whose execution jump-starts cellular processes, including the processes that lead to self-organization of networks that regulate execution of the genetic digital code — the gene regulatory networks. A separate digital code also has a central role in the operation of those gene regulatory networks: the code adjacent to a gene determines which transcription regulating factors can bind there, and thereby controls gene activity. In other words, a digital code, separate from the code that specifies the proteins of the gene regulatory networks, gives specificity to the behavior of those networks and to their regulation of the execution of the genetic digital code.[53] Eventually, digital codes surrender to decipherment, offering the hope that we might someday read the message of living and find ways to edit it.
Further elaborating beyond the thermodynamic, evolutionary, self-organizational, autonomous agent and network perspectives we might say that:
A living system has the informational content and information-processing faculty to remain for a time in a near steady-state as a self-organized system of hierarchical robust modular networks. It works autonomously to offset responses to perturbations and to reproduce itself, enabled by the influx of energy and matter and by a more than compensatory efflux of waste (disorder), thereby exploiting a far-from-equilibrium state. Finally, it is capable of participating in the transgenerational evolution of the species to which it belongs in adapting to changing environments. |
Organic chemistry as informatics
Why the central place of carbon in the chemistry of all earth’s living things? The physical chemistry of carbon allows it to bond with many other elements, especially hydrogen, oxygen, nitrogen and phosphorus, and, even to form carbon-to-carbon bonds. The avidity for carbon to bond to itself allows carbon atoms to easily join into long chains and closed rings; and allows small organic molecules (such as sugars, amino acids and nucleotides) to join into huge macromolecules that are remarkably stable at standard conditions. These macromolecules are the repositories of information used by living entities.
The variety of carbon bonds vary in strength as well as in 3-D conformation; adding a dynamic quality to many organic molecules. The simplest set of bonds that carbon can form is that of a tetrahedron, or pyramid. Other types of bonds involve more than one shared electron, and for that reason are called double, and triple bonds; importantly, these different bonds constitute three entirely different geometries. Changing from one type of carbon-to-carbon bond to another type, as when a double bond is reduced to a single bond, will cause energy changes but without destroying the molecule. Such changes not only affect free energy, but also affect the actual shape of the molecule and the particular side groups attached to it. In this way, for at least some organic molecules, the 'pulse of life' is represented at an atomic level.
These properties of carbon mean that organic macromolecules are capable of containing tremendous 'banks' of information coded in their very structure. Not only can each of the constituent molecules be huge, but several categories of chemicals, like nucleotides or amino acids, that contain several different species, can be ordered so that the possible combinations are effectively limitless. All of these molecules are involved in the molecular-interaction networks of cells. Amogst these networks of interactions are those that enable cells to import and transform energy and energy-rich matter from the environment and that ultimately enable cells to grow, survive and reproduce.
Elsewhere in the universe, where conditions differ greatly from earth’s, other elements may hold a central place in life. Silicon, carbon's close relative on the periodic table, also forms bonds with itself, but they have little stability under conditions compatible with life as we know it. In places in the universe where physical conditions might favor silicon-based macromolecules, silicon-based life might exist.[54]
Identifying the different scientific perspectives on life
The different perspectives biologists use in viewing living systems can be identified as follows:
- Living systems import energy, matter, and information from their environment, and export waste. This flow enables living systems to organize and maintain themselves, and thus to delay (for their lifetime) the dictate of the Second Law of Thermodynamics, that organized systems ultimately degrade to a state of randomness;
- The basic building blocks of all living systems are cells; the basic (genetic) information that generates cells comes as part of their starting materials. This information, in the form of nucleic acid macromolecules, encodes many different types of proteins that interact to assemble an organization that can import energy and export waste. Cells inherit this information from ‘parent’ cells, raising two as yet unanswered questions: how did cells arise in the first place? and how did they acquire stores of information?;[55] (see Origin of life and Evolution of cells)
- The molecular interactions are governed by the universal laws of physics and chemistry; those laws, together with the inherited information, enable a self-organizing system that can work autonomously for survival and reproduction, and allow properties to emerge that could not be anticipated from those of the system's components alone.
- The activities of a living system have no 'master controller'; they need only a type of organization that maintains the system far-from-equilibrium, which can yield improbable self-organized structures and activities.
- Living things cannot escape from changing external conditions, so they must exhibit robustness in their organization and must be adaptable to maintain their stability. Robustness and adaptability derive from the properties of a hierarchical network of subnetworks of molecular circuits;
- Living systems must produce enough reproductive variability to allow evolution through natural selection, which guides the continuation of a 3.5 billion year history of Earth’s living world. By evolution, living systems generate increasing varieties of living systems, occupy an extreme spectrum of environments, create their own environments,[56] and permit sufficient complexity to enable them to process information in a way that allows them to ‘experience’ themselves.
Synthesis of perspectives on what constitutes Life
The activity of living, for a cell-based system, depends on the ability to maintain a near steady-state of organized functioning far from the state of randomness. The system achieves that in part because of its location in the path of a downhill gradient of flowing energy. It exploits that gradient through its abilities to import some of the energy flowing past it and to export unusable energy and material, thus increasing its own order at the expense of a more than counterbalancing disorder of its surroundings.
Those principles seem to apply to all living systems: single cells, multicellular organs and organisms, and multi-organism demes and ecosystems.
The building block and working unit of all living systems is the cell. For cells to utilize available external energy or energy-rich matter and achieve order, they must have, from the outset, some informational content. That enables the cell to produce components that can, by molecular interactions, respond to the imported energy and material to organize themselves. That organization comprises modular networks of molecular interactions, and networks of interacting networks — self-organized and coordinated functional interactions. The properties of the networks and those of the hierarchy of networks enable the system to perpetuate itself, and to maintain its steady-state despite fluctuations in environmental factors. That principle, too, applies to all living systems. Any organism, plant or animal, comprises a network of organs working autonomously, maintaining its steady-state functioning far from equilibrium in response to environmental perturbations — physiologists refer to that as homeostasis.
The networks that regulate the flow of information through the cell were 'designed' by natural selection and other evolutionary processes. That is, the codes that evolved by natural selection were those which produced molecules that could interact in ways that contribute to self-organization of those networks that enable a cell to sustain and reproduce itself. The collaboration of natural selection and physico-chemical laws perpetuates living systems not only in real-time but also in geological, or ‘evolutionary’, time. From common ancestors — however they may have arisen (see Evolution of cells) — informationally-guided, self-organizing, autonomous network dynamics enabled generation of the diversity of all living systems on the planet, over a period of more than three billion years. Living systems perpetuate living systems, exploiting free energy on its inexorable path to dissipation and degradation, and harvesting energy in developing systems organization by a more than counterbalancing dis-organizing of the larger system in which it is embedded.
Further reading
- Books
- Schrodinger E (1944-2000) What is Life? Cambridge University Press (Canto). ISBN 0-521-42708-8 Chapter 6: Order, Disorder and Entropy (Prediction of hereditary molecule like a coded periodic crystal — Watson claims inspiration — Stresses open thermodynamic systems key to life.)
- Kaneko K (2006) Life: An Introduction to Complex Systems Biology. Springer, Berlin ISBN 3-540-32666-9
- Dill KA, Bromberg S, Stigter D (2003) Molecular Driving Forces: Statistical Thermodynamics in Chemistry and Biology. Garland Science, New York. ISBN 0-8153-2051-5
- Strogatz SH (2003) Sync: The Emerging Science of Spontaneous Order. Theia, New York ISBN 0-7868-6844-9
- Buchanan M (2002) Nexus: Small Worlds and the Groundbreaking Science of Networks. W.W. Norton, New York ISBN 0-393-04153-0
- Hoagland M, Dodson B, Hauck J (2001) Exploring the Way Life Works: The Science of Biology. Jones and Bartlett Publishers, Inc, Mississauga, Ontario ISBN 0-7637-1688-X (For young people. An illustrated text.)
- Solé R, Goodwin B (2000) Signs of Life: How Complexity Pervades Biology. Basic Books, Perseus Books Group, New York ISBN 0-465-01928-5
- Loewenstein WR (2000) The Touchstone of life: Molecular Information, Cell Communication, and the Foundations of Life. Oxford University Press ISBN 0-19-514057-5 Book Review and Chapter One
- Hoagland M, Dodson B (1998) The Way Life Works: The Science Lovers Illustrated Guide to How Life Grows, Develops, Reproduces, and Gets Along. Three Rivers Press, New York ISBN 0-8129-2888-1 (For young people. An illustrated text.)
- Margulis L, Sagan D (1995) What is Life? Simon & Schuster ISBN 0-684-81087-5
- Articles
- Epstein IR, Pojman JA, Steinbock O (2006) Introduction: Self-organization in nonequilibrium chemical systems. Chaos 16:037101 PMID 17014235
- Hazen R (2006) The Big Questions: What is Life? New Scientist Issue 2578, 46-51
- Marenduzzo D et al. (2006) Entropy-driven genome organization. Biophys J 90:3712-21 PMID 16500976
- Morowitz H, Smith E (2006) Energy flow and the organization of life
- Scheffer M, van Nes EH (2006) Self-organized similarity, the evolutionary emergence of groups of similar species. Proc Natl Acad Sci USA 103:6230-5 PMID 16585519
- Walsh DM (2006) Organisms as natural purposes: The contemporary evolutionary perspective. Studies in History and Philosophy of Science. Part C: Studies in History and Philosophy of Biological and Biomedical Sciences 37:771-91 37:771-91
- Park K et al. (2005) Self-organized scale-free networks. Phys Rev E Stat Nonlin Soft Matter Phys 72:026131 PMID 16196668
- Troisi A et al.(2005) An agent-based approach for modeling molecular self-organization. Proc Natl Acad Sci USA 102:255-60 PMID 15625108
- Pace NR (2001) Special Feature: The universal nature of biochemistry. Proc Natl Acad Sci USA 98:805-8
- Dronamraju KR (1999) Erwin Schrodinger and the origins of molecular biology. Genetics 153:1071-6 PMID 10545442
- Interviews and Commentaries
- Kauffman S. The Adjacent Possible: A Talk with Stuart Kauffman
See also in Citizendium
External links not cited above
- From the preface: "How life on Earth got going is still mysterious, but not for want of ideas."
- Excerpt from Conclusion: "“Living organisms are autopoietic systems: self-constructing, self-maintaining, energy-transducing autocatalytic entities” in which information needed to construct the next generation of organisms is stabilized in nucleic acids that replicate within the context of whole cells and work with other developmental resources during the life-cycles of organisms, but they are also “systems capable of evolving by variation and natural selection: self-reproducing entities, whose forms and functions are adapted to their environment and reflect the composition and history of an ecosystem” (Harold 2001, 232)."
Appendix A
Living things share some very specific features not always explicitly stated above. For example,
- some evidence supports the proposition that all extant living things descended from a common ancestor [57] Other evidence suggests that "Extant life on Earth is descended not from one, but from three distinctly different cell types. However, the designs of the three have developed and matured, in a communal fashion, along with those of many other designs that along the way became extinct." [58]
- only pre-existing cells can 'manufacture' new cells;
- only pre-existing multicellular organisms can manufacture new multicellular organisms;
- a membrane encloses every cell, protecting each from dissolution into its external environment;
- the cell membrane contains molecular systems that enables the cell to import usable matter and energy and to export unusable matter and energy, and others that enable it to send and receive signals to and from other cells;
- all cells and multicellular systems eventually die.
Appendix B
Selected definitions of life
Marcello Bárbieri, Professor of Morphology and Embryology at the University of Ferrara, Italy, collected an extensive list of definitions of “Life” from scientists and philosophers of the 19th and 20th centuries.[59] Those selected below resonate with the systems and thermodynamic perspectives of living systems:
- "The broadest and most complete definition of life will be "the continuous adjustment of internal to external relations". — Herbert Spencer (1884)
- "It is the particular manner of composition of the materials and processes, their spatial and temporal organisation which constitute what we call life." — A. Putter (1923)
- "A living organism is a system organised in a hierarchic order of many different parts, in which a great number of processes are so disposed that by means of their mutual relations, within wide limits with constant change of the materials and energies constituting the system, and also in spite of disturbances conditioned by external influences, the system ts generated or remains in the state characteristic of it, or these processes lead to the production of similar systems." — L. von Bertalanffy (1933)
- "Life seems to be an orderly and lawful behaviour of matter, not based exclusively on its tendency to go from order to disorder, but based partly on existing order that is kept up." — E. Schrodinger (1944)
- "Life is made of three basic elements: matter, energy and information. Any element in life that is not matter and energy can be reduced to information." — P. Fong (1973)
- "A living system is an open system that is self-replicating, self-regulating, and feeds on energy from the environment." — R. Sattler (1986)
Published collections of definitions of 'Life'
- Popa R (2004) Chronology of Definitions and Interpretations of Life. In: Popa R (ed.) Between Necessity and Probability: Searching for the Definition and Origin of Life. Berlin: Springer-Verlag 2004: pp 197-205 (Quotes and source-citations from 1885 to 2002)
- Barbieri M (2003) Appendix: Definitions of Life. In: The Organic Codes: An Introduction to Semantic Biology. Cambridge, UK: Cambridge University Press ISBN 0521824141 (Quotes from 1802 to 2002)
The gray zone
Not all entities that otherwise qualify as living reproduce themselves, although they exist as reproduced living things. Biologists call such living things 'sterile'. Examples include programmed sterility (e.g., worker ants, mules); acquired sterility (due to acquired injury (disease) to the reproductive process; access sterility (lack of reproductive fitness); voluntary sterility (e.g., human couples). Obviously living things with the capacity to reproduce may die before reaching the reproductive stage in their life-cycle. Conversely, non-reproducing individuals may still effect reproduction of copies of their genes by facilitating the reproduction of kin, who share many genes (see kin selection).
Viruses would not qualify strictly as living things, but manage to 'reproduce' in living systems.
One might ask whether a spermatozoon qualifies as a living entity. From the thermodynamic perspective, one might answer affirmatively, as it keeps itself ‘living’ by doing cellular work. It has a compartmentalized internal organization functioning to keep it far-from-equilibrium. In that respect it resembles a motile bacterium. A spermatozoon reproduces, but in a different way than a motile bacterium: it does it through its parent’s progeny, which the spermatozoon plays an essential role in generating. It doesn’t have to hijack a cell’s machinery to reproduce; it cooperates with another cell (an ovum) to generate cells with machinery to reproduce it. Moreover, in reproducing that way, it subjects itself to meiotic crossover variation, just as its parent’s progeny does, contributing to the variation needed by natural selection to perpetuate the process of living on an earth with ever-changing environments.
References
Citations and Notes
- ↑ Note: Some words, so-called ‘semantic primes’ have distinct meanings not definable in terms of other words. Ultimately, all definitions converge on about 70 semantic primes that occur universally among languages. Semantic primes include the verb ‘live’ but not the noun ‘life’. (Semantic Primes and Cultural Scripts in Language: Learning and Intercultural Communication.)
Carol Cleland of NASA’s Astrobiology Institute suggests that scientists are not really interested in what the word 'life' happens to mean in our language. "What we really need to focus on is coming up with an adequately general theory of living systems, as opposed to a definition of 'life'."Carol Cleland on "What is Life?" - ↑ De Duve C (2004) Life Evolving: Molecules, Mind, and Meaning. Oxford University Press. New York ISBN 0195156056
- ↑ from Robinson R (2007) Both barriers and trait complementarity govern pollination network structure. PLoS Biol 5(2): e54 doi:10.1371/journal.pbio.0050054
- ↑ Valentine JW et al. (1994) Morphological complexity increase in metazoans. Paleobiology 20:131-42
- ↑ Woese CR et al. (1990) Towards a natural system of organisms: proposal for the domains archaea, bacteria, and eucarya. Proc Natl Acad Sci USA 87:4576-9
- ↑ Note: Other boundaries of living systems include bark, shells, cell walls, skin, fur, and structures of the physical environment.
- ↑ How Many Genes Are in the Human Genome? at the Human Genome Project Information website hosted by the U.S. Department of Energy
- ↑ (a) The UniProtKB/Swiss-Prot Human Proteome Initiative [1]; (b) Norregaard Jensen O. (2004) Modification-specific proteomics: characterization of post-translational modifications by mass spectrometry. Current Opinion in Chemical Biology 8:33-41
- ↑ Valentine JW et al. (1994) Morphological complexity increase in metazoans. Paleobiology 20:131-42
Note: See the article, Cell, for a more thorough discussion of 'cell types'. - ↑ Andrea Falcon (2006) Aristotle on Causality
- ↑ Bothwell JHF. (2006) The long past of systems biology. New Phytologist 170:6-10 Link to Full-Text.
Note: We might interpret Aristotle's four components of 'causality' as four components of 'explanation', for as Bothwell writes: “Aristotle (384-322 BC) wanted to search for explanations of natural events that inspire wonder. His search led him to conclude that any question which might be asked about the behaviour of a complex, apparently designed, system might be answered if we knew four properties of that system. He called these the aitiai, a word which is usually rendered into English as 'causes', but which may be better translated as 'explanations' (Aristotle, APst 90a7-94b34; CA 715a1-17 [Aristotle. APst (Posterior Analytics), Trans: H. Tredennick (1960). Harvard University Press, Loeb Classical Library. (ISBN 0-674-99430-2)]).” - ↑ Note: For example, physical chemists cannot predict the properties of water from knowledge of its components, hydrogen and oxygen. The way hydrogen and water interact to form H2O, and the way H2O molecules interact, enables the properties of water to 'emerge'.
- ↑ Note: Following up on the example of water, the properties of its environment (e.g., temperature, pressure) affect the way the H2O molecules organize themselves, as ice, or liquid, or steam
- ↑ Note: In relation to downward causation, the environment’s effect can sometimes reach down to the genetic recipe with molecular signals, altering the recipe’s expression and consequently the characteristics of the cells — so-called 'epigenetic' effects. When epigenetic alterations of gene expression occur in the reproductive organs, the system changes can be transmitted to the next generation. See
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- ↑ Note: A random pattern of parts has no order (it has maximum entropy) and no information. A living system has order in its organized functions, has computationally-rich informational content, and low entropy.
- ↑ Note: At birth, the Universe received a global energy account. The total energy of the Universe always remains constant, but if and when it completely disperses itself as heat into many little accounts, it has degraded to the point it can no longer do work. At that point the Universe has reached a state of absent energy gradients: a state of equilibrium characterized by complete randomness.
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- ↑ Note: Unless contrived to do work, heat has a disordering, entropy-increasing effect. The more heat put into a system at a given temperature, the greater the entropy. At lower temperatures, the same heat input can increase entropy more, because the greater degree of order present at lower temperatures means a greater fractional increase in disorder.
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- ↑ Note: ....or the progeny of some conspecific living systems. Many living systems coexist with similar living systems, constituting a 'species', or group of 'conspecifics'.
- ↑ Jablonka E, Lamb MJ (2005) Evolution in Four Dimension: Genetic, Epigenetic, Behavioral, and Symbolic Variation in the History of Life. Cambridge: The MIT Press
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- ↑ See Evolution of cells
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- ↑ Note: The qualifier "in part" reflects the need to invoke not only molecular self-assembly but also evolutionary mechanisms selecting genes that yield proteins whose chemical properties enable interactions that tend to optimize functional self-organization — in other words, adaption to circumstances. One must also invoke local real-time selective processes that confer stability and appropriate functionality to molecular self-assembly, called homeostasis. Self-organization and adaptation conjoin to yield function.
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- ↑ Dawkins R (1988) The Blind Watchmaker: Why the Evidence of Evolution Reveals a Universe Without Design. New York: W.W. Norton & Company, Inc. ISBN 0393304485 Excerpt from Amazon.com review: “The title of this 1986 work, Dawkins's second book, refers to the Rev. William Paley's 1802 work, Natural Theology, which argued that, just as finding a watch would lead you to conclude that a watchmaker must exist, the complexity of living organisms proves that a Creator exists. Not so, says Dawkins: "the only watchmaker in nature is the blind forces of physics, albeit deployed in a very special way... it is the blind watchmaker." Physics, of course, includes open-system non-equilibrium thermodynamics.
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- ↑ Note: This article takes the view that cells underlie ‘living systems’, and that cellular subsystems, like transcription networks and metabolic pathways, qualify as ‘biological systems’ but not as ‘living systems’.
- ↑ Note: That does not explain the origin of the ability to utilize available energy and materials. To explain that requires knowledge of the origin of living systems. See Origin of life
- ↑ Note: Usable energy, also called ‘free energy’, in virtue of its organized state that flows downhill to dissipated uselessness, has all the attributes of information.
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