Volume 69, Issue 8
ORIGINAL ARTICLE

The definition, recognition, and interpretation of convergent evolution, and two new measures for quantifying and assessing the significance of convergence

C. Tristan Stayton

E-mail address: tstayton@bucknell.edu

Department of Biology, Bucknell University, 337 Biology Building, Lewisburg, Pennsylvania, 17837

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First published: 15 July 2015
Citations: 86

Abstract

Convergent evolution is an important phenomenon in the history of life. Despite this, there is no common definition of convergence used by biologists. Instead, several conceptually different definitions are employed. The primary dichotomy is between pattern‐based definitions, where independently evolved similarity is sufficient for convergence, and process‐based definitions, where convergence requires a certain process to produce this similarity. The unacknowledged diversity of definitions can lead to problems in evolutionary research. Process‐based definitions may bias researchers away from studying or recognizing other sources of independently evolved similarity, or lead researchers to interpret convergent patterns as necessarily caused by a given process. Thus, pattern‐based definitions are recommended. Existing measures of convergence are reviewed, and two new measures are developed. Both are pattern based and conceptually minimal, quantifying nothing but independently evolved similarity. One quantifies the amount of phenotypic distance between two lineages that is closed by subsequent evolution; the other simply counts the number of lineages entering a region of phenotypic space. The behavior of these measures is explored in simulations; both show acceptable Type I and Type II error. The study of convergent evolution will be facilitated if researchers are explicit about working definitions of convergence and adopt a standard toolbox of convergence measures.

Number of times cited according to CrossRef: 86

  • Co‐evolution of cleaning and feeding morphology in western Atlantic and eastern Pacific gobies, Evolution, 10.1111/evo.13904, 74, 2, (419-433), (2020).
  • Cave‐adapted evolution in the North American amblyopsid fishes inferred using phylogenomics and geometric morphometrics, Evolution, 10.1111/evo.13958, 74, 5, (936-949), (2020).
  • Divergent adaptations in resource‐use traits explain how pikas thrive on the roof of the world, Functional Ecology, 10.1111/1365-2435.13609, 34, 9, (1826-1838), (2020).
  • Fungus-growing insects host a distinctive microbiota apparently adapted to the fungiculture environment, Scientific Reports, 10.1038/s41598-020-68448-7, 10, 1, (2020).
  • Macroevolutionary convergence connects morphological form to ecological function in birds, Nature Ecology & Evolution, 10.1038/s41559-019-1070-4, (2020).
  • Convergent evolution of olfactory and thermoregulatory capacities in small amphibious mammals, Proceedings of the National Academy of Sciences, 10.1073/pnas.1917836117, (201917836), (2020).
  • Incomplete convergence of gliding mammal skeletons, Evolution, 10.1111/evo.14094, 0, 0, (2020).
  • Current Options for Visualization of Local Deformation in Modern Shape Analysis Applied to Paleobiological Case Studies, Frontiers in Earth Science, 10.3389/feart.2020.00066, 8, (2020).
  • 3D Geometric Morphometrics Reveals Convergent Character Displacement in the Central European Contact Zone between Two Species of Hedgehogs (Genus Erinaceus), Animals, 10.3390/ani10101803, 10, 10, (1803), (2020).
  • Convergent evolution in lemur environmental niches, Journal of Biogeography, 10.1111/jbi.13741, 47, 4, (795-806), (2019).
  • Tail Weaponry in Ankylosaurs and Glyptodonts: An Example of a Rare but Strongly Convergent Phenotype, The Anatomical Record, 10.1002/ar.24093, 303, 4, (988-998), (2019).
  • Pleiotropic jaw morphology links the evolution of mechanical modularity and functional feeding convergence in Lake Malawi cichlids, Proceedings of the Royal Society B: Biological Sciences, 10.1098/rspb.2018.2358, 286, 1897, (20182358), (2019).
  • Integrating natural history collections and comparative genomics to study the genetic architecture of convergent evolution, Philosophical Transactions of the Royal Society B: Biological Sciences, 10.1098/rstb.2018.0248, 374, 1777, (20180248), (2019).
  • The role of bite force in the evolution of head shape and head shape dimorphism in Anolis lizards, Functional Ecology, 10.1111/1365-2435.13438, 33, 11, (2191-2202), (2019).
  • Phylogenetic Comparative Methods and the Evolution of Multivariate Phenotypes, Annual Review of Ecology, Evolution, and Systematics, 10.1146/annurev-ecolsys-110218-024555, 50, 1, (405-425), (2019).
  • Comparative analysis of squamate brains unveils multi-level variation in cerebellar architecture associated with locomotor specialization, Nature Communications, 10.1038/s41467-019-13405-w, 10, 1, (2019).
  • Evolution of a soft‐tissue foraging adaptation in African cichlids: Roles for novelty, convergence, and constraint, Evolution, 10.1111/evo.13824, 73, 10, (2072-2084), (2019).
  • Leaf shape and size track habitat transitions across forest–grassland boundaries in the grass family (Poaceae), Evolution, 10.1111/evo.13722, 73, 5, (927-946), (2019).
  • Ancient and contingent body shape diversification in a hyperdiverse continental fish radiation, Evolution, 10.1111/evo.13658, 73, 3, (569-587), (2019).
  • Ecomorphological convergence in Eleutherodactylus frogs: a case of replicate radiations in the Caribbean, Ecology Letters, 10.1111/ele.13246, 22, 5, (884-893), (2019).
  • Developmental tuning of mineralization drives morphological diversity of gill cover bones in sculpins and their relatives, Evolution Letters, 10.1002/evl3.128, 3, 4, (374-391), (2019).
  • Weighing homoplasy against alternative scenarios with the help of macroevolutionary modeling: A case study on limb bones of fossorial sciuromorph rodents, Ecology and Evolution, 10.1002/ece3.5592, 9, 19, (11025-11039), (2019).
  • Morphometric convergence among European sand gobies in freshwater (Gobiiformes: Gobionellidae), Ecology and Evolution, 10.1002/ece3.5375, 9, 14, (8087-8103), (2019).
  • Macroevolution of arboreality in salamanders, Ecology and Evolution, 10.1002/ece3.5267, 9, 12, (7005-7016), (2019).
  • Evolution of cranial shape in a continental‐scale evolutionary radiation of Australian lizards, Evolution, 10.1111/evo.13851, 73, 11, (2216-2229), (2019).
  • Multiple convergent events created a nominal widespread species: Triplophysa stoliczkae (Steindachner, 1866) (Cobitoidea: Nemacheilidae), BMC Evolutionary Biology, 10.1186/s12862-019-1503-3, 19, 1, (2019).
  • Running in circles in phylomorphospace: host environment constrains morphological diversification in parasitic wasps, Proceedings of the Royal Society B: Biological Sciences, 10.1098/rspb.2018.2352, 286, 1895, (20182352), (2019).
  • Repeated Evolution of Divergent Modes of Herbivory in Non-avian Dinosaurs, Current Biology, 10.1016/j.cub.2019.10.050, (2019).
  • Morphology, Ecology, and Biogeography of Independent Origins of Cleaning Behavior Around the World, Integrative and Comparative Biology, 10.1093/icb/icz030, (2019).
  • A new, fast method to search for morphological convergence with shape data, PLOS ONE, 10.1371/journal.pone.0226949, 14, 12, (e0226949), (2019).
  • Heterochronic Shifts Mediate Ecomorphological Convergence in Skull Shape of Microcephalic Sea Snakes, Integrative and Comparative Biology, 10.1093/icb/icz033, (2019).
  • Wasp waist and flight: convergent evolution in wasps reveals a link between wings and body shapes, The American Naturalist, 10.1086/706914, (2019).
  • Use and misuse of discrete character data for morphospace and disparity analyses, Palaeontology, 10.1111/pala.12407, 62, 2, (305-319), (2018).
  • The convergent evolution of snake‐like forms by divergent evolutionary pathways in squamate reptiles*, Evolution, 10.1111/evo.13651, 73, 3, (481-496), (2018).
  • Convergent evolution of an extreme dietary specialisation, the olfactory system of worm-eating rodents, Scientific Reports, 10.1038/s41598-018-35827-0, 8, 1, (2018).
  • The ecological origins of snakes as revealed by skull evolution, Nature Communications, 10.1038/s41467-017-02788-3, 9, 1, (2018).
  • Study of morphological variation of northern Neotropical Ariidae reveals conservatism despite macrohabitat transitions, BMC Evolutionary Biology, 10.1186/s12862-018-1152-y, 18, 1, (2018).
  • Detecting the molecular basis of phenotypic convergence, Methods in Ecology and Evolution, 10.1111/2041-210X.13071, 9, 11, (2170-2180), (2018).
  • Journeys through discrete‐character morphospace: synthesizing phylogeny, tempo, and disparity, Palaeontology, 10.1111/pala.12380, 61, 5, (637-645), (2018).
  • Phenotypic disparity of the elbow joint in domestic dogs and wild carnivores*, Evolution, 10.1111/evo.13503, 72, 8, (1600-1613), (2018).
  • Trait‐specific processes of convergence and conservatism shape ecomorphological evolution in ground‐dwelling squirrels, Evolution, 10.1111/evo.13422, 72, 3, (473-489), (2018).
  • The shadow of the past: Convergence of young and old South American desert lizards as measured by head shape traits, Ecology and Evolution, 10.1002/ece3.4548, 8, 23, (11399-11409), (2018).
  • Phylo-Allometric Analyses Showcase the Interplay between Life-History Patterns and Phenotypic Convergence in Cleaner Wrasses, The American Naturalist, 10.1086/697047, 191, 5, (E129-E143), (2018).
  • Non-uniform evolutionary response of gecko eye size to changes in diel activity patterns, Biology Letters, 10.1098/rsbl.2018.0064, 14, 5, (20180064), (2018).
  • Convergent evolution in the Euarchontoglires, Biology Letters, 10.1098/rsbl.2018.0366, 14, 8, (20180366), (2018).
  • Trophic specialization drives morphological evolution in sea snakes, Royal Society Open Science, 10.1098/rsos.172141, 5, 3, (172141), (2018).
  • The influence of multiple functional demands on morphological diversification: A test on turtle shells, Evolution, 10.1111/evo.13561, 72, 9, (1933-1949), (2018).
  • Delayed trait development and the convergent evolution of shell kinesis in turtles, Proceedings of the Royal Society B: Biological Sciences, 10.1098/rspb.2018.1585, 285, 1888, (20181585), (2018).
  • Phylogenetic, ecological and biomechanical constraints on larval form: A comparative morphological analysis of barnacle nauplii, PLOS ONE, 10.1371/journal.pone.0206973, 13, 11, (e0206973), (2018).
  • Phylogenetic Comparative Methods can Provide Important Insights into the Evolution of Toxic Weaponry, Toxins, 10.3390/toxins10120518, 10, 12, (518), (2018).
  • Digitizing extant bat diversity: An open-access repository of 3D μCT-scanned skulls for research and education, PLOS ONE, 10.1371/journal.pone.0203022, 13, 9, (e0203022), (2018).
  • Convergence in the functional properties of forelimb muscles in carnivorans: adaptations to an arboreal lifestyle?, Biological Journal of the Linnean Society, 10.1093/biolinnean/bly123, (2018).
  • Evolution of skull shape in the family Salamandridae (Amphibia: Caudata), Journal of Anatomy, 10.1111/joa.12759, 232, 3, (359-370), (2017).
  • Genome of the Tasmanian tiger provides insights into the evolution and demography of an extinct marsupial carnivore, Nature Ecology & Evolution, 10.1038/s41559-017-0417-y, 2, 1, (182-192), (2017).
  • Feeding ecology is the primary driver of beak shape diversification in waterfowl, Functional Ecology, 10.1111/1365-2435.12890, 31, 10, (1985-1995), (2017).
  • Phylogenetic convergence and multiple shell shape optima for gliding scallops (Bivalvia: Pectinidae), Journal of Evolutionary Biology, 10.1111/jeb.13137, 30, 9, (1736-1747), (2017).
  • Developmental dynamics of ecomorphological convergence in a transcontinental lizard radiation, Evolution, 10.1111/evo.13186, 71, 4, (936-948), (2017).
  • Labrid cleaner fishes show kinematic convergence as juveniles despite variation in morphology, The Journal of Experimental Biology, 10.1242/jeb.153783, 220, 15, (2787-2797), (2017).
  • Convergent Phenotypic Evolution despite Contrasting Demographic Histories in the Fauna of White Sands, The American Naturalist, 10.1086/692138, 190, S1, (S44-S56), (2017).
  • Pattern and Process in the Comparative Study of Convergent Evolution, The American Naturalist, 10.1086/692648, 190, S1, (S13-S28), (2017).
  • Functional convergence and phenotypic divergence in two specialist species of pine-associated ladybirds, Evolutionary Ecology, 10.1007/s10682-017-9918-z, 31, 6, (885-898), (2017).
  • Radiating despite a Lack of Character: Ecological Divergence among Closely Related, Morphologically Similar Honeyeaters (Aves: Meliphagidae) Co-occurring in Arid Australian Environments, The American Naturalist, 10.1086/690008, 189, 2, (E14-E30), (2017).
  • The evolution of the platyrrhine talus: A comparative analysis of the phenetic affinities of the Miocene platyrrhines with their modern relatives, Journal of Human Evolution, 10.1016/j.jhevol.2017.07.015, 111, (179-201), (2017).
  • Convergent body shapes have evolved via deterministic and historically contingent pathways in Lerista lizards, Biological Journal of the Linnean Society, 10.1093/biolinnean/blx040, 121, 4, (858-875), (2017).
  • Convergence, Evolutionary Developmental Biology, 10.1007/978-3-319-33038-9, (1-12), (2017).
  • Reaffirming ‘Ethnobotanical Convergence’, Trends in Plant Science, 10.1016/j.tplants.2017.06.001, 22, 8, (640-641), (2017).
  • Evolutionary ecomorphology of the Falkland Islands wolf Dusicyon australis, Mammal Review, 10.1111/mam.12085, 47, 2, (159-163), (2017).
  • Rare ecomorphological convergence on a complex adaptive landscape: Body size and diet mediate evolution of jaw shape in squirrels (Sciuridae), Evolution, 10.1111/evo.13168, 71, 3, (633-649), (2017).
  • Approaches to Macroevolution: 1. General Concepts and Origin of Variation, Evolutionary Biology, 10.1007/s11692-017-9420-0, 44, 4, (427-450), (2017).
  • Camouflage Variations on a Theme of the Nymphalid Ground Plan, Diversity and Evolution of Butterfly Wing Patterns, 10.1007/978-981-10-4956-9, (39-58), (2017).
  • Swimming and running: a study of the convergence in long bone morphology among semi-aquatic mustelids (Carnivora: Mustelidae), Biological Journal of the Linnean Society, 10.1093/biolinnean/blw027, 121, 1, (38-49), (2017).
  • Widespread ecomorphological convergence in multiple fish families spanning the marine–freshwater interface, Proceedings of the Royal Society B: Biological Sciences, 10.1098/rspb.2017.0565, 284, 1854, (20170565), (2017).
  • A rich diversity of opercle bone shape among teleost fishes, PLOS ONE, 10.1371/journal.pone.0188888, 12, 12, (e0188888), (2017).
  • Morphological convergence in ‘river dolphin’ skulls, PeerJ, 10.7717/peerj.4090, 5, (e4090), (2017).
  • Quantification provides a conceptual basis for convergent evolution, Biological Reviews, 10.1111/brv.12257, 92, 2, (815-829), (2016).
  • Convergent evolution in social swallows (Aves: Hirundinidae), Ecology and Evolution, 10.1002/ece3.2641, 7, 2, (550-560), (2016).
  • Parallel selective pressures drive convergent diversification of phenotypes in pythons and boas, Ecology Letters, 10.1111/ele.12620, 19, 7, (800-809), (2016).
  • Environmental constraints and call evolution in torrent‐dwelling frogs, Evolution, 10.1111/evo.12903, 70, 4, (811-826), (2016).
  • Repeated evolution of carnivory among Indo‐Australian rodents, Evolution, 10.1111/evo.12871, 70, 3, (653-665), (2016).
  • Analysing Convergent Evolution: A Practical Guide to Methods, Evolutionary Biology, 10.1007/978-3-319-41324-2, (23-36), (2016).
  • Convergence as an Evolutionary Trade-off in the Evolution of Acoustic Signals: Echolocation in Horseshoe Bats as a Case Study, Evolutionary Biology, 10.1007/978-3-319-41324-2, (89-103), (2016).
  • Brain shape convergence in the adaptive radiation of New World monkeys, Proceedings of the National Academy of Sciences, 10.1073/pnas.1514473113, 113, 8, (2158-2163), (2016).
  • Convergent Evolution Provides Evidence of Similar Radiations in Shell Shape in the Turtle Families Emydidae and Geoemydidae, Herpetologica, 10.1655/HERPETOLOGICA-D-15-00037, 72, 2, (120-129), (2016).
  • Road Map to Study Convergent Evolution: A Proposition for Evolutionary Systems Biology Approaches, Evolutionary Biology, 10.1007/978-3-319-41324-2, (3-21), (2016).
  • Ecomorphological convergence in planktivorous surgeonfishes, Journal of Evolutionary Biology, 10.1111/jeb.12837, 29, 5, (965-978), (2016).
  • What does convergent evolution mean? The interpretation of convergence and its implications in the search for limits to evolution, Interface Focus, 10.1098/rsfs.2015.0039, 5, 6, (20150039), (2015).

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