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Convergent evolution is the independent evolution of similar features in species of different lineages. Convergent evolution creates analogous structures that have similar form or function, but that were not present in the last common ancestor of those groups. The cladistic term for the same phenomenon is homoplasy, from Greek for same form. The recurrent evolution of flight is a classic example of convergent evolution. Flying insects, birds, and bats have all evolved the capacity of flight independently. They have "converged" on this useful trait.
Functionally similar features arising through convergent evolution are termed analogous, in contrast to homologous structures or traits, which have a common origin, but not necessarily similar function. The British anatomist Richard Owen was the first scientist to recognise the fundamental difference between analogies and homologies. Bat and pterosaur wings constitute an example of analogous structures, while the bat wing is homologous to human and other mammal forearms, sharing an ancestral state despite serving different functions. The opposite of convergent evolution is divergent evolution, whereby related species evolve different traits. On a molecular level, this can happen due to random mutation unrelated to adaptive changes; see long branch attraction.
Convergent evolution is similar to, but distinguishable from, the phenomena of parallel evolution. Parallel evolution occurs when two independent but similar species evolve in the same direction and thus independently acquire similar characteristics—for instance gliding frogs have evolved in parallel from multiple types of tree frog.
- 1 Causes
- 2 Significance
- 3 Distinctions
- 4 Examples
- 5 See also
- 6 Further reading
- 7 References
In morphology, analogous traits will often arise where different species live in similar ways and/or similar environment, and so face the same environmental factors. When occupying similar ecological niches (that is, a distinctive way of life) similar problems lead to similar solutions.
In biochemistry, physical and chemical constraints on mechanisms cause some active site arrangements to independently evolve multiple times in separate enzyme superfamilies (for example, see also catalytic triad).
Convergence has been associated with Darwinian evolution in the popular imagination since at least the 1940s. For example, Elbert A. Rogers argued: "If we lean toward the theories of Darwin might we not assume that man was [just as] apt to have developed in one continent as another?"
In his book Wonderful Life, Stephen Jay Gould argues that if the tape of life were re-wound and played back, life would have taken a very different course. Simon Conway Morris disputes this conclusion, arguing that convergence is a dominant force in evolution, and given that the same environmental and physical constraints are at work, life will inevitably evolve toward an "optimum" body plan, and at some point, evolution is bound to stumble upon intelligence, a trait presently identified with at least primates, corvids, and cetaceans.
Convergence is difficult to quantify, so progress on this issue may require exploitation of engineering specifications (as of wing aerodynamics) and comparably rigorous measures of "very different course" in terms of phylogenetic (molecular) distances.
Convergent evolution is a topic touched by many different fields of biology, many of which use slightly different nomenclature. This section attempts to clarify some of those terms.
In cladistics, a homoplasy or a homoplastic character state is a trait (genetic, morphological etc.) that is shared by two or more taxa because of convergence, parallelism or reversal. Homoplastic character states require extra steps to explain their distribution on a most parsimonious cladogram. Homoplasy is only recognizable when other characters imply an alternative hypothesis of grouping, because in the absence of such evidence, shared features are always interpreted as similarity due to common descent. Homoplasious traits or changes (derived trait values acquired in unrelated organisms in parallel) can be compared with synapomorphy (a derived trait present in all members of a monophyletic clade), autapomorphy (derived trait present in only one member of a clade), or apomorphies, derived traits acquired in all members of a monophyletic clade following divergence where the most recent common ancestor had the ancestral trait (the ancestral trait manifesting in paraphyletic species as a plesiomorphy).
Re-evolution vs. convergent evolution
In some cases, it is difficult to tell whether a trait has been lost then re-evolved convergently, or whether a gene has simply been 'switched off' and then re-enabled later. Such a re-emerged trait is called an atavism. From a mathematical standpoint, an unused gene (selectively neutral) has a steadily decreasing probability of retaining potential functionality over time. The time scale of this process varies greatly in different phylogenies; in mammals and birds, there is a reasonable probability of remaining in the genome in a potentially functional state for around 6 million years.
Parallel vs. convergent evolution
For a particular trait, proceeding in each of two lineages from a specified ancestor to a later descendant, parallel and convergent evolutionary trends can be strictly defined and clearly distinguished from one another. However the cutoff point for what is considered convergent and what is considered parallel evolution is assigned somewhat arbitrarily. When two species are similar in a particular character, evolution is defined as parallel if the ancestors were also similar and convergent if they were not. However, this definition is somewhat murky. All organisms share a common ancestor more or less recently, so the question of how far back to look in evolutionary time and how similar the ancestors need to be for one to consider parallel evolution to have taken place is not entirely resolved within evolutionary biology. Some scientists have argued parallel evolution and convergent evolution are more or less indistinguishable from one another. Others have argued that we should not shy away from the gray area and that there are still important distinctions between parallel and convergent evolution.
When the ancestral forms are unspecified or unknown, or the range of traits considered is not clearly specified, the distinction between parallel and convergent evolution becomes more subjective. For instance, the striking example of similar placental and marsupial forms is described by Richard Dawkins in The Blind Watchmaker as a case of convergent evolution, because mammals on each continent had a long evolutionary history prior to the extinction of the dinosaurs under which to accumulate relevant differences. Stephen Jay Gould describes many of the same examples as parallel evolution starting from the common ancestor of all marsupials and placentals. Many evolved similarities can be described in concept as parallel evolution from a remote ancestor, with the exception of those where quite different structures are co-opted to a similar function. For example, consider Mixotricha paradoxa, a microbe that has assembled a system of rows of apparent cilia and basal bodies closely resembling that of ciliates but that are actually smaller symbiont micro-organisms, or the differently oriented tails of fish and whales. On the converse, any case in which lineages do not evolve together at the same time in the same ecospace might be described as convergent evolution at some point in time.
The definition of a trait is crucial in deciding whether a change is seen as divergent, or as parallel or convergent. In the image above, note that, since serine and threonine possess similar structures with an alcohol side-chain, the example marked "divergent" would be termed "parallel" if the amino acids were grouped by similarity instead of being considered individually. As another example, if genes in two species independently become restricted to the same region of the animals through regulation by a certain transcription factor, this may be described as a case of parallel evolution — but examination of the actual DNA sequence will probably show only divergent changes in individual base-pair positions, since a new transcription factor binding site can be added in a wide range of places within the gene with similar effect.
A similar situation occurs considering the homology of morphological structures. For example, many insects possess two pairs of flying wings. In beetles, the first pair of wings is hardened into wing covers with little role in flight, while in flies the second pair of wings is condensed into small halteres used for balance. If the two pairs of wings are considered as interchangeable, homologous structures, this may be described as a parallel reduction in the number of wings, but otherwise the two changes are each divergent changes in one pair of wings.
Similar to convergent evolution, evolutionary relay describes how independent species acquire similar characteristics through their evolution in similar ecosystems, but not at the same time (dorsal fins of sharks and ichthyosaurs).
Protease active sites
The enzymology of proteases provides some of the clearest examples of convergent evolution. These examples reflect the intrinsic chemical constraints on enzymes, leading evolution to independently converge on equivalent solutions repeatedly.
Serine and cysteine proteases use different amino acid functional groups (alcohol or thiol) as a nucleophile. In order to activate that nucleophile, they orient an acidic and basic residue in a catalytic triad. The chemical and physical constraints on enzyme catalysis have caused identical triad arrangements to have evolved independently over 20 times in different enzyme superfamilies.
Threonine proteases use the amino acid threonine as their catalytic nucleophile. Unlike cysteine and serine, threonine is a secondary alcohol (i.e. has a methyl group). The methyl group of threonine greatly restricts the possible orientations of triad and substrate as the methyl clashes with either the enzyme backbone or histidine base. Consequently, most threonine proteases use an N-terminal threonine in order to avoid such steric clashes. Several evolutionarily independent enzyme superfamilies with different protein folds use the N-terminal residue as a nucleophile. This commonality of active site but difference of protein fold indicates that the active site evolved convergently in those families.
As more sequence data are becoming available, there is growing interest in convergent changes at the level of DNA and amino acids. In 2013 the first genome-wide study of convergence was published. Comparisons of the genomes of echolocating bats and the dolphin identified numerous convergent amino acid substitutions in genes implicated in hearing and vision.
A classic comparison is between the marsupial fauna of Australia and the placental mammals of the Old World. The two lineages are clades—that is, they each share a common ancestor that belongs to their own group, and are more closely related to one another than to any other clade—but very similar forms evolved in each isolated population. Many body plans, for instance sabre-toothed cats and flying squirrels, evolved independently in both populations. The same streamlined shape has been converged upon by fish (e.g., herrings), marine mammals (e.g., dolphins) and even the extinct ichthyosaur (Mesozoic era). This bodyplan is an adaptation to being an active predator in a high drag environment. It is also debated whether earless seals and eared seals are a single marine group, or represent two separate episodes of carnivorans turning to a marine environment.
A classical example of an analogy is the ability to fly in birds and bats. Both groups can move by powered flight, but flight has evolved independently in the two groups. The ability to fly does not make birds and bats close relatives. The ancestors of both bats and birds were terrestrial quadrupeds, and each has independently evolved powered flight via adaptations of their forelimbs. Although both forelimb adaptations are superficially "wing-shaped," they are substantially dissimilar in construction. The bat wing is a membrane stretched across four extremely elongated fingers, while the airfoil of the bird wing is made of feathers, which are strongly attached to the forearm (the ulna) and the highly fused bones of the wrist and hand (the carpometacarpus), with only tiny remnants of two fingers remaining, each anchoring a single feather. (Both bats and birds have retained the thumb for specialized functions.) So, while the wings of bats and birds are functionally convergent, they are not anatomically convergent.
Similarly, the extinct pterosaur also shows an independent evolution of vertebrate forelimb to wing. An even more distantly related group with wings is the insects, they not only evolved separately as wings, but from totally different organs, starting from a fundamentally different bodyplan.
One of the most well-known examples of convergent evolution is the camera eye of cephalopods (e.g., squid), vertebrates (e.g., mammals) and cnidaria (e.g., box jellies). Their last common ancestor had at most a very simple photoreceptive spot, but a range of processes led to the progressive refinement of this structure to the advanced camera eye — with one subtle difference: The cephalopod eye is "wired" in the opposite direction, with blood and nerve vessels entering from the back of the retina, rather than the front as in vertebrates.
Insect mouthparts show many examples of organs which can be used to study convergent evolution in the context of form and function. The mouthparts of different insect groups consist of a set of homologous organs, specialised to the function of dietary intake of that insect group (which can be experimentally quantified). Convergent Evolution of many groups of insects led from original biting-chewing mouthparts to different derived function types. They build a proboscis at flower-visiting insects for example, which are able to ingest food very efficiently or biting-sucking mouthparts, showing different function mechanisms at different groups of blood-sucking insects.
Convergent evolution is commonly noted when considering the morphology of animal species, but there are many diverse examples of the phenomenon in plant biology as well, such as the multiple origins of C4 photosynthesis. A true fruit such as an apple incorporates one or more ovules and their accessory tissues, but many edible plant-derived tissues commonly regarded as fruits actually arise from very different embryological structures. This implies a convergent process in which genetically unrelated precursors assume a common form under selective pressure, in this case the competition for seed dispersal through consumption by animals. The emergence of seed dispersal by ants (myrmecochory), which has evolved independently more than 100 times and is present in more than 11,000 plant species, is also considered one of the most dramatic examples of convergent evolution in biology. 
- McGhee, George R. (2011). Convergent Evolution: Limited Forms Most Beautiful. Vienna Series in Theoretical Biology, Massachusetts Institute of Technology Press, Cambridge (MA). 322 pp. ISBN 978-0-262-01642-1
- Rasmussen, L. E. L.; Lee, Terry D.; Roelofs, Wendell L.; Zhang, Aijun; Daves, G. Doyle (1996). "Insect pheromone in elephants". Nature 379 (6567): 684. Bibcode:1996Natur.379..684R. doi:10.1038/379684a0. PMID 8602213.
- Convergent Evolution Examples- Ecological Equivalents, Department of Biology, Bellarmine University.
- Stearns, S. & Hoekstra, R. 2005. Evolution: An introduction.
- Lowe, Nancy, "Single Centers of Creation", Southern Spaces, 30 November 2009.
- McMenamin, Mark A. S. (1998). The Garden of Ediacara: Discovering the First Complex Life. Columbia University Press. ISBN 978-0-231-10558-3
- Map of Life : Convergent Evolution Online — University of Cambridge
- Reece, J, Meyers, N, Urry, L, Cain, M, Wasserman, S, Minorsky, P, Jackson, R, Cooke, B,. Cambell Biology, 9th Edition. Pearson. p. 472. ISBN 9781442531765.
- Lomolino, M, Riddle, B, Whittaker, R, Brown, J. Biogeography, Fourth Edition. Sinauer Associates, Inc. p. 426. ISBN 978-0-878-93-494-2.
- Thunstad, Erik (2009). Darwins teori, evolusjon gjennom 400 år (in Norwegian). Oslo, Norway: Humanist forlag. p. 404. ISBN 978-82-92622-53-7.
- Online Biology Glossary.
- Buller, AR; Townsend, CA (Feb 19, 2013). "Intrinsic evolutionary constraints on protease structure, enzyme acylation, and the identity of the catalytic triad.". Proceedings of the National Academy of Sciences of the United States of America 110 (8): E653–61. doi:10.1073/pnas.1221050110. PMID 23382230.
- Rogers, E. A. 1943. "Who knows?" Hobbies—The Magazine for Collectors, June 1943, p. 101.
- Gould, S.J. (1989). Wonderful Life: The Burgess Shale and the Nature of History. W.W. Norton & Company.[page needed]
- Conway Morris, Simon (2005). Life's solution: inevitable humans in a lonely universe. Cambridge, UK: Cambridge University Press. doi:10.2277/0521827043. ISBN 0-521-60325-0. OCLC 156902715.
- Chirat, R.; Moulton, D. E.; Goriely, A. (2013). "Mechanical basis of morphogenesis and convergent evolution of spiny seashells". Proceedings of the National Academy of Sciences 110 (15): 6015. doi:10.1073/pnas.1220443110.
- Hennig, W., Phylogenetic Systematics. University of Illinois Press, Urbana IL, 1966.
- Collin, R.; Cipriani, R. (2003). "Dollo's law and the re-evolution of shell coiling". Proceedings of the Royal Society B 270 (1533): 2551–2555. doi:10.1098/rspb.2003.2517. PMC 1691546. PMID 14728776.
- Zhang, J.; Kumar, S. (1997). "Detection of convergent and parallel evolution at the amino acid sequence level" (PDF). Mol. Biol. Evol. 14: 527–36. doi:10.1093/oxfordjournals.molbev.a025789.
- ARENDT, J; REZNICK, D (January 2008). "Convergence and parallelism reconsidered: what have we learned about the genetics of adaptation?". Trends in Ecology & Evolution 23 (1): 26–32. doi:10.1016/j.tree.2007.09.011.
- Pearce, T. (10 November 2011). "Convergence and Parallelism in Evolution: A Neo-Gouldian Account". The British Journal for the Philosophy of Science 63 (2): 429–448. doi:10.1093/bjps/axr046.
- Dawkins, Richard (1986). The Blind Watchmaker. W. W. Norton & Company, Inc. pp. 100–106. ISBN 0-393-31570-3.
- Dodson, G; Wlodawer, A (September 1998). "Catalytic triads and their relatives.". Trends in Biochemical Sciences 23 (9): 347–52. doi:10.1016/S0968-0004(98)01254-7. PMID 9787641.
- Ekici, OD; Paetzel, M; Dalbey, RE (December 2008). "Unconventional serine proteases: variations on the catalytic Ser/His/Asp triad configuration.". Protein science : a publication of the Protein Society 17 (12): 2023–37. doi:10.1110/ps.035436.108. PMID 18824507.
- Parker, J; Tsagkogeorga, G; Cotton, JA; Liu, Y; Provero, P; Stupka, E; Rossiter, SJ (2013). "Genome-wide signatures of convergent evolution in echolocating mammals". Nature 502 (7470): , 228–231. doi:10.1038/nature12511.
- Tietjen, William J. "Convergent Evolution Examples – Ecological Equivalents". The Spider Lab: The Internet's True Web Page. Louisville, KY, USA: Bellarmine University Department of Biology. Retrieved 2009-03-07.[dead link]
- Lento, G.M., Hickson, R.E., Chambers, G.K., Penny, D. (1 January 1995). "Use of spectral analysis to test hypotheses on the origin of pinnipeds". Molecular Biology and Evolution 12 (1): 28–52. doi:10.1093/oxfordjournals.molbev.a040189. PMID 7877495.
- Roberts MBV (1986) Biology: A Functional Approach Nelson Thornes, page 274. ISBN 9780174480198.
- Kozmik, Z; Ruzickova, J; Jonasova, K; Matsumoto, Y.; Vopalensky, P.; Kozmikova, I.; Strnad, H.; Kawamura, S.; Piatigorsky, J; Paces, V; Vlcek, C (1 July 2008). "From the Cover: Assembly of the cnidarian camera-type eye from vertebrate-like components". Proceedings of the National Academy of Sciences 105 (26): 8989–8993. doi:10.1073/pnas.0800388105. PMC 2449352. PMID 18577593. Retrieved 3 May 2013.
- Krenn, Harald W.; Plant, John D.; Szucsich, Nikolaus U. (2005). "Mouthparts of flower-visiting insects". Arthropod Structure & Development 34 (1): 1–40. doi:10.1016/j.asd.2004.10.002.
- Krenn, Harald W.; Gereben-Krenn, Barbara-Amina; Steinwender, Bernhardt M.; Popov, Alexi (2008). "Flower visiting Neuroptera: Mouthparts and feeding behaviour of Nemoptera sinuata (Nemopteridae)". European Journal of Entomology 105 (2): 267–77. doi:10.14411/eje.2008.037.
- Bauder, Julia A.S.; Lieskonig, Nora R.; Krenn, Harald W. (2011). "The extremely long-tongued Neotropical butterfly Eurybia lycisca (Riodinidae): Proboscis morphology and flower handling". Arthropod Structure & Development 40 (2): 122–7. doi:10.1016/j.asd.2010.11.002.
- Wilhelmi, Andreas P.; Krenn, Harald W. (2012). "Elongated mouthparts of nectar-feeding Meloidae (Coleoptera)". Zoomorphology 131 (4): 325–37. doi:10.1007/s00435-012-0162-3.
- Williams BP, Johnston IG, Covshoff S, Hibberd JM (September 2013). "Phenotypic landscape inference reveals multiple evolutionary paths to C4 photosynthesis". eLife 2: e00961. doi:10.7554/eLife.00961.
- Lorts C, Briggeman T, Sang T (2008). "Evolution of fruit types and seed dispersal: A phylogenetic and ecological snapshot" (PDF). Journal of Systematics and Evolution 46 (3): 396–404. doi:10.3724/SP.J.1002.2008.08039.
- Lengyel Sz, Gove AD, Latimer AM, Majer JD, Dunn RR (2010). "Convergent evolution of seed dispersal by ants, and phylogeny and biogeography in flowering plants: a global survey". Perspectives in Plant Ecology, Evolution and Systematics 12: 43–55. doi:10.1016/j.ppees.2009.08.001.