Coevolution
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In biology, coevolution is "the change of a biological object triggered by the change of a related object."[1] Coevolution can occur at many biological levels: it can be as microscopic as correlated mutations between amino acids in a protein, or as macroscopic as covarying traits between different species in an environment. Each party in a coevolutionary relationship exerts selective pressures on the other, thereby affecting each other's evolution. Coevolution of different species includes the evolution of a host species and its parasites (host–parasite coevolution), and examples of mutualism evolving through time. Evolution in response to abiotic factors, such as climate change, is not biological coevolution (since climate is not alive and does not undergo biological evolution).
The general conclusion is that coevolution may be responsible for much of the genetic diversity seen in normal populations including: blood plasma polymorphism, protein polymorphism, histocompatibility systems, etc.[2]
There is little evidence of coevolution driving large-scale changes in Earth's history, since abiotic factors such as mass extinction and expansion into ecospace seem to guide the shifts in the abundance of major groups.[3] However, there is evidence for coevolution at the level of populations and species. For example, the concept of coevolution was briefly described by Charles Darwin in On the Origin of Species, and developed in detail in Fertilisation of Orchids.[4][5][6] It is likely that viruses and their hosts may have coevolved in various scenarios.[7]
The parasite host relationship is probably what drove the prevalence of sexual reproduction over the more efficient asexual reproduction. It seems that most sources determine that when a host is infected by a parasite, sexual reproduction affords a chance of resistance, through variation in the next generation, giving sexual reproduction viability for fitness not seen in the asexual reproduction, which would only generate another generation of the organism susceptible to infection by the same parasite.[8]
Coevolution is primarily a biological concept, but has been applied by analogy to fields such as computer science, sociology / International Political Economy[9] and astronomy.
Models
One model of coevolution was Leigh Van Valen's Red Queen's Hypothesis, which states that "for an evolutionary system, continuing development is needed just in order to maintain its fitness relative to the systems it is co-evolving with".[10] This hypothesis predicts that sexual reproduction allows a host to stay just ahead of its parasite by a generation, similar to the Red Queen in “Through the Looking Glass”. …always running ….. Just ahead. The essence is that the host reproduces sexually giving it immunity over its parasite, which then evolves in response. This requires the next generation to repeat the sequence.[11] Emphasizing the importance of sexual conflict, Thierry Lodé described the role of antagonist interactions in evolution, giving rise to a concept of antagonist coevolution.[12] Coevolution branching strategies for asexual population dynamics in limited resource environments have been modeled using the generalized Lotka–Volterra equations.[13] A model based on adaptive dynamics and experimental data of floral and proboscis lengths, as well as nectar consumed and pollen deposited during the pollination of the long-tubed iris (Lapeirousia anceps) by the long-proboscid fly (Moegistorhynchus longirostris) has generated diverse coevolutionary dynamics, including two types of Red Queen dynamics, evolutionary branching (backed by observations of coexisting irises of short and long tubes in a single population) and trap.[14]
Coevolution types
Diffuse coevolution between pairs of entities (often referred to as pairwise coevolution) exists, such as that between predator and prey, host and symbiont or host and parasite, but many cases are less clearcut: a species may evolve in response to a number of other species, each of which is also evolving in response to a set of species.
Specific coevolution involves a single species interacting with another producing an adaptation, wherein the other species evolves an adaptation to counteract the original specie's adaptation.
Escape and radiate coevolution occurs when an organism under selectional constraints by predation develops a defense mechanism allowing it to "escape", and then "radiate" into another species entirely. The predator then evolves accordingly, and the process continues.
Specific examples
Hummingbirds and ornithophilous flowers
Hummingbirds and ornithophilous (bird-pollinated) flowers have evolved a mutualistic relationship. The flowers have nectar suited to the birds' diet, their color suits the birds' vision and their shape fits that of the birds' bills. The blooming times of the flowers have also been found to coincide with hummingbirds' breeding seasons.
Flowers have converged to take advantage of similar birds.[15] Flowers compete for pollinators, and adaptations reduce unfavourable effects of this competition.[15] Bird-pollinated flowers usually have higher volumes of nectar and higher sugar production than those pollinated by insects.[16] This meets the birds' high energy requirements, which are the most important determinants of their flower choice.[16] Following their respective breeding seasons, several species of hummingbirds occur at the same locations in North America, and several hummingbird flowers bloom simultaneously in these habitats. These flowers seem to have converged to a common morphology and color.[16] Different lengths and curvatures of the corolla tubes can affect the efficiency of extraction in hummingbird species in relation to differences in bill morphology.[16] Tubular flowers force a bird to orient its bill in a particular way when probing the flower, especially when the bill and corolla are both curved; this also allows the plant to place pollen on a certain part of the bird's body.[16] This opens the door for a variety of morphological co-adaptations.
An important requirement for attraction is conspicuousness to birds, which reflects the properties of avian vision and habitat features.[16] Birds have their greatest spectral sensitivity and finest hue discrimination at the red end of the visual spectrum,[16] so red is particularly conspicuous to them. Hummingbirds may also be able to see ultraviolet "colors".[16] The prevalence of ultraviolet patterns and nectar guides in nectar-poor entomophilous (insect-pollinated) flowers warns the bird to avoid these flowers.[16]
Hummingbirds form the family Trochilidae, whose two subfamilies are the Phaethornithinae (hermits) and the Trochilinae. Each subfamily has evolved in conjunction with a particular set of flowers. Most Phaethornithinae species are associated with large monocotyledonous herbs, while the Trochilinae prefer dicotyledonous plant species.[16]
Angraecoid orchids and African moths
Angraecoid orchids and African moths coevolve because the moths are dependent on the flowers for nectar and the flowers are dependent on the moths to spread pollen so they can reproduce. Coevolution has led to deep flowers and moths with long probosci.
Old world swallowtail and fringed rue
An example of antagonistic coevolution is the old world swallowtail (Papilio machaon) caterpillar living on the fringed rue (Ruta chalepensis) plant. The rue produces etheric oils which repel plant-eating insects. The old world swallowtail caterpillar developed resistance to these poisonous substances, thus reducing competition with other plant-eating insects.
Garter snake and rough-skinned newt
Coevolution of predator and prey species is illustrated by the Rough-skinned newt (Taricha granulosa) and the common garter snake (Thamnophis sirtalis). The newts produce a potent neurotoxin that concentrates in their skin. Garter snakes have evolved resistance to this toxin through a series of genetic mutations, and prey upon the newts. The relationship between these animals has resulted in an evolutionary arms race that has driven toxin levels in the newt to extreme levels. This is an example of coevolution because differential survival caused each organism to change in response to changes in the other.
California buckeye and pollinators
When beehives are populated with bee species that have not coevolved with the California buckeye (Aesculus californica), sensitivity to aesculin, a neurotoxin present in its nectar, may be noticed; this sensitivity is only thought to be present in honeybees and other insects that did not coevolve with A. californica.[17]
Acacia ant and bullhorn acacia tree
The acacia ant (Pseudomyrmex ferruginea) protects the bullhorn acacia (Acacia cornigera) from preying insects and from other plants competing for sunlight, and the tree provides nourishment and shelter for the ant and its larvae.[18] Nevertheless, some ant species can exploit trees without reciprocating, and hence have been given various names such as 'cheaters', 'exploiters', 'robbers' and 'freeloaders'. Although cheater ants do important damage to the reproductive organs of trees, their net effect on host fitness is difficult to forecast and not necessarily negative.[19]
Yucca Moth and the yucca plant
Coevolution outside biology
Coevolution is primarily a biological concept, but has been applied to other fields by analogy.
Biological Applications
The study of coevolution in natural populations could help in fields such as conservation, human epidemiology, and improved agriculture.
Technological coevolution
Computer software and hardware can be considered as two separate components but tied intrinsically by coevolution. Similarly, operating systems and computer applications, web browsers and web applications. All of these systems depend upon each other and advance step by step through a kind of evolutionary process. Changes in hardware, an operating system or web browser may introduce new features that are then incorporated into the corresponding applications running alongside.[22] The idea is closely related to the concept of "joint optimization" in sociotechnical systems analysis and design. STS suggests that all human systems include both a "technical system" encompassing the tools and hardware used for production and maintenance, and a "social system" of relationships and procedures through which the technology is tied into the goals of the system and all the other human and organizational relationships within and outside the system. It is possible for the system to optimize on the technology, giving priority to technical solutions and compelling the social system to adapt to it; or to optimize on the social system, giving priority to existing social patterns and procedures and compelling the technology to fill in what gaps remain. In practice, both solutions are generally suboptimal in terms of outcomes. Better outcomes are usually obtained by a reciprocal process of joint optimization, through which both the technical system and the social system change to some degree in response to each other. This may happen naturally, but it is usually best achieved by a systematic process of sociotechnical design in which both systems are led to recognize each other's value and purposes and their mutual adaptation is negotiated between them.[23]
Algorithms
Coevolutionary algorithms are a class of algorithms used for generating artificial life as well as for optimization, game learning and machine learning. Coevolutionary methods have been applied by Daniel Hillis, who coevolved sorting networks, and Karl Sims, who coevolved virtual creatures.
Cosmology and astronomy
In his book The Self-organizing Universe, Erich Jantsch attributed the entire evolution of the cosmos to coevolution.
In astronomy, an emerging theory states that black holes and galaxies develop in an interdependent way analogous to biological coevolution.[24]
See also
- Bak–Sneppen model
- Character displacement
- Co-adaptation
- Coextinction
- Genomics of domestication
- Modular evolution
- Parallel evolution
- Convergent evolution
- Sexual conflict
- Lynn Margulis
- Technological evolution
- Sympatric speciation, the creation of two or more species from an ancestor species based on something other than spatial divergence (i.e., geography).
- Ecological fitting
References
- ↑ Yip et al.; Patel, P; Kim, PM; Engelman, DM; McDermott, D; Gerstein, M (2008). "An integrated system for studying residue coevolution in proteins". Bioinformatics 24 (2): 290–292. doi:10.1093/bioinformatics/btm584. PMID 18056067.
- ↑ Anderson, R., and May, R.(1982), Coevolution of hosts and parasites, Parasitology, Cambridge Journals, retrieved from http://journals.cambridge.org/action/displayAbstract?fromPage=online&aid=4133104
- ↑ Sahney, S., Benton, M.J. and Ferry, P.A. (2010). "Links between global taxonomic diversity, ecological diversity and the expansion of vertebrates on land" (PDF). Biology Letters 6 (4): 544–547. doi:10.1098/rsbl.2009.1024. PMC 2936204. PMID 20106856.
- ↑ Thompson, John N. (1994). The coevolutionary process. Chicago: University of Chicago Press. ISBN 0-226-79760-0. Retrieved 2009-07-27.
- ↑ Darwin, Charles (1859). On the Origin of Species (1st ed.). London: John Murray. Retrieved 2009-02-07.
- ↑ Darwin, Charles (1877). On the various contrivances by which British and foreign orchids are fertilised by insects, and on the good effects of intercrossing (2nd ed.). London: John Murray. Retrieved 2009-07-27.
- ↑ C.Michael Hogan. 2010. Virus. Encyclopedia of Earth. Editors: Cutler Cleveland and Sidney Draggan
- ↑ Editors (2011), Sexual reproduction works thanks to ever-evolving host, parasite relationships: study, Physorg, retrieved fromhttp://phys.org/news/2011-07-sexual-reproduction-ever-evolving-host-parasite.html
- ↑ For example, See Jessop, Bob., 2004, 'Critical Semiotic Analysis and Critical Political Economy', in Critical Discourse Studies 1 (1):1–16.
- ↑ Van Valen L. (1973): "A New Evolutionary Law", Evolutionary Theory 1, pp. 1–30. Cited in: The Red Queen Principle
- ↑ Sterns, S. (2009), Coevolution, EEB-122: Principles of evolution, ecology, and behavior, Open Yale Courses, retrieved from http://oyc.yale.edu/ecology-and-evolutionary-biology/eeb-122/lecture-20
- ↑ Lodé, Thierry (2007). La guerre des sexes chez les animaux, une histoire naturelle de la sexualité. Paris: Odile Jacob. ISBN 2-7381-1901-8.
- ↑ G. S. van Doorn, F. J. Weissing (April 2002). "Ecological versus Sexual Selection Models of Sympatric Speciation: A Synthesis". Selection (Budapest, Hungary: Akadémiai Kiadó) 2 (1-2): 17–40. doi:10.1556/Select.2.2001.1-2.3. ISSN 1585-1931. 1588-287X. Retrieved 2009-09-15. "The intuition behind the occurrence of evolutionary branching of ecological strategies in resource competition was confirmed, at least for asexual populations, by a mathematical formulation based on Lotka–Volterra type population dynamics. (Metz et al., 1996)."
- ↑ Zhang, F., Hui, C. & Pauw, A. (2013) Adaptive divergence in Darwin’s race: how coevolution can generate trait diversity in a pollination system. Evolution, 67: 548-560.
- ↑ 15.0 15.1 Brown James H., Kodric-Brown Astrid (1979). "Convergence, Competition, and Mimicry in a Temperate Community of Hummingbird-Pollinated Flowers". Ecology 60 (5): 1022–1035. doi:10.2307/1936870.
- ↑ 16.0 16.1 16.2 16.3 16.4 16.5 16.6 16.7 16.8 16.9 Stiles, F. Gary (1981). "Geographical Aspects of Bird Flower Coevolution, with Particular Reference to Central America". Annals of the Missouri Botanical Garden 68 (2): 323–351. doi:10.2307/2398801.
- ↑ C. Michael Hogan (13 September 2008). California Buckeye: Aesculus californica, GlobalTwitcher.com
- ↑ National Geographic. "Acacia Ant Video".
- ↑ Palmer TM, Doak DF, Stanton ML, Bronstein JL, Kiers ET, Young TP, Goheen JR, Pringle RM (2010). "Synergy of multiple partners, including freeloaders, increases host fitness in a multispecies mutualism". Proceedings of the National Academy of Sciences of the United States of America 107 (40): 17234–9. doi:10.1073/pnas.1006872107. PMC 2951420. PMID 20855614.
- ↑ Hemingway, Claire (2004). "Pollination Partnerships Fact Sheet" (PDF). Flora of North America: 1–2. Retrieved 2011-02-18. "Yucca and Yucca Moth"
- ↑ Pellmyr, Olle; James Leebens-Mack (August 1999). "Forty million years of mutualism: Evidence for Eocene origin of the yucca-yucca moth association" (PDF). Proc. Natl. Acad. Sci. USA 96 (16): 9178–9183. doi:10.1073/pnas.96.16.9178. PMC 17753. PMID 10430916. Retrieved 2011-02-18.
- ↑ Theo D’Hondt, Kris De Volder, Kim Mens and Roel Wuyts, Co-Evolution of Object-Oriented Software Design and Implementation, TheKluwer International Series in Engineering and Computer Science, 2002, Volume 648, Part 2, 207–224, DOI: 10.1007/978-1-4615-0883-0_7
- ↑ A. Cherns (1976). "The principles of sociotechnical design". In: Human Relations. Vol 29(8)
- ↑ Britt, Robert. "The New History of Black Holes: 'Co-evolution' Dramatically Alters Dark Reputation".
Further reading
- Dawkins, R. Unweaving the Rainbow.
- Futuyma, D. J. and M. Slatkin (editors) (1983). Coevolution. Sunderland, Massachusetts: Sinauer Associates. pp. 555 pp. ISBN 0-87893-228-3.
- Geffeney, Shana L., et al. "Evolutionary diversification of TTX-resistant sodium channels in a predator-prey interaction". Nature 434 (2005): 759–763.
- Michael Pollan The Botany of Desire: A Plant's-eye View of the World. Bloomsbury. ISBN 0-7475-6300-4. Account of the co-evolution of plants and humans
- Thompson, J. N. (1994). The Coevolutionary Process. Chicago: University of Chicago Press. pp. 376 pp. ISBN 0-226-79759-7.
- Mintzer, Alex; Vinson, S.B. "Kinship and incompatibility between colonies of the acacia ant Pseudomyrex ferruginea". Behavioral Ecology and Sociobiology 17 (1): 75–78. Abstract
- Armstrong, W.P. "The Yucca and its Moth". Wayne's Word. Palomar College. Retrieved 2011-03-29.
External links
- Coevolution, video of lecture by Stephen C. Stearns (Open Yale Courses)