Autapomorphy

In phylogenetics, an autapomorphy is a distinctive feature, known as a derived trait, that is unique to a given taxon. That is, it is found only in one taxon, but not found in any others or outgroup taxa, not even those most closely related to the focal taxon (which may be a species, family or in general any clade).[2] It can therefore be considered an apomorphy in relation to a single taxon.[3] The word autapomorphy, introduced in 1950 by German entomologist Willi Hennig, is derived from the Greek words αὐτός, autos "self"; ἀπό, apo "away from"; and μορφή, morphḗ = "shape".[4]

Phylogenies showing the terminology used to describe different patterns of ancestral and derived character or trait states.[1]

Discussion

Because autapomorphies are only present in a single taxon, they do not convey information about relationship. Therefore, autapomorphies are not useful to infer phylogenetic relationships. However, autapomorphy, like synapomorphy and plesiomorphy is a relative concept depending on the taxon in question. An autapomorphy at a given level may well be a synapomorphy at a less-inclusive level.[5] An example of an autapomorphy can be described in modern snakes. Snakes have lost the two pairs of legs that characterize all of Tetrapoda, and the closest taxa to Ophidia – as well as their common ancestors – all have two pairs of legs. Therefore, the Ophidia taxon presents an autapomorphy with respect to its absence of legs.[3]

The autapomorphic species concept is one of many methods that scientists might use to define and distinguish species from one another. This definition assigns species on the basis of amount of divergence associated with reproductive incompatibility, which is measured essentially by number of autapomorphies.[6] This grouping method is often referred to as the "monophyletic species concept" or the "phylospecies" concept and was popularized by D.E. Rosen in 1979. Within this definition, a species is seen as "the least inclusive monophyletic group definable by at least one autapomorphy".[7] While this model of speciation is useful in that it avoids non-monophyletic groupings, it has its criticisms as well. N.I. Platnick, for example, believes the autapomorphic species concept to be inadequate because it allows for the possibility of reproductive isolation and speciation while revoking the "species" status of the mother population. In other words, if a peripheral population breaks away and becomes reproductively isolated, it would conceivably need to develop at least one autapomorphy to be recognized as a different species. If this can happen without the larger mother population also developing a new autapomorphy, then the mother population cannot remain a species under the autapomorphic species concept: it would no longer have any apomorphies not also shared by the daughter species.[8]

Phylogenetic similarities: These phylogenetic terms are used to describe different patterns of ancestral and derived character or trait states as stated in the above diagram in association with synapomorphies.[1]

  • Homoplasy in biological systematics is when a trait has been gained or lost independently in separate lineages during evolution. This convergent evolution leads to species independently sharing a trait that is different from the trait inferred to have been present in their common ancestor.[9][10][11]
    • Parallel Homoplasy – derived trait present in two groups or species without a common ancestor due to convergent evolution.[12]
    • Reverse Homoplasy – trait present in an ancestor but not in direct descendants that reappears in later descendants.[13]
  • Apomorphy – a derived trait. Apomorphy shared by two or more taxa and inherited from a common ancestor is synapomorphy. Apomorphy unique to a given taxon is autapomorphy.[14][15][16][17]
    • Synapomorphy/Homology – a derived trait that is found in some or all terminal groups of a clade, and inherited from a common ancestor, for which it was an autapomorphy (i.e., not present in its immediate ancestor).
    • Underlying synapomorphy – a synapomorphy that has been lost again in many members of the clade. If lost in all but one, it can be hard to distinguish from an autapomorphy.
    • Autapomorphy – a distinctive derived trait that is unique to a given taxon or group.[3]
  • Symplesiomorphy – an ancestral trait shared by two or more taxa.
    • Plesiomorphy – a symplesiomorphy discussed in reference to a more derived state.
    • Pseudoplesiomorphy – is a trait that cannot be identified as neither a plesiomorphy nor an apomorphy that is a reversal.[18]
  • Reversal – is a loss of derived trait present in ancestor and the reestablishment of a plesiomorphic trait.
  • Convergence – independent evolution of a similar trait in two or more taxa.
  • Hemiplasy[19][20]

References
  1. Page RD, Holmes EC (14 July 2009). Molecular Evolution: A Phylogenetic Approach. John Wiley & Sons. ISBN 978-1-4443-1336-9. OCLC 609843839.
  2. Futuyma DJ (1998). Evolutionary Biology (3rd ed.). Sinauer Associates, Inc. p. 95.
  3. Appel RD, Feytmans E (2009). "Chapter 3: Introduction of Phylogenetics and its Molecular Aspects". Bioinformatics: a Swiss Perspective (1st ed.). World Scientific Publishing Company.
  4. Calow PP (2009). Encyclopedia of Ecology and Environmental Management. John Wiley & Sons. ISBN 978-1-4443-1324-6. OCLC 1039167559.
  5. Forey PL (1997). History of the Coelacanth Fishes (1st ed.). Sprinter.
  6. Howard DJ, Berlocher SH (1998). Endless Forms: Species and Speciation (1st ed.). USA: Oxford University Press. ISBN 978-0-19-510901-6. OCLC 60181901.
  7. Bull AT (2004). Microbial Diversity and Bioprospecting. ASM Press.
  8. Platnick NI (2001). "From Cladograms to Classifications: The Road to DePhylocode." (PDF). The Systematics Association.
  9. Gauger A (April 17, 2012). "Similarity Happens! The Problem of Homoplasy". Evolution Today & Science News.
  10. Sanderson MJ, Hufford L (21 October 1996). Homoplasy: The Recurrence of Similarity in Evolution. Elsevier. ISBN 978-0-08-053411-4. OCLC 173520205.
  11. Brandley MC, Warren DL, Leaché AD, McGuire JA (April 2009). "Homoplasy and clade support". Systematic Biology. 58 (2): 184–98. doi:10.1093/sysbio/syp019. PMID 20525577.
  12. Archie JW (September 1989). "Homoplasy Excess Ratios: New Indices for Measuring Levels of Homoplasy in Phylogenetic Systematics and a Critique of the Consistency Index". Systematic Zoology. 38 (3): 253–269. doi:10.2307/2992286. JSTOR 2992286.
  13. Wake DB, Wake MH, Specht CD (February 2011). "Homoplasy: from detecting pattern to determining process and mechanism of evolution". Science. 331 (6020): 1032–5. Bibcode:2011Sci...331.1032W. doi:10.1126/science.1188545. PMID 21350170. S2CID 26845473.
  14. Simpson MG (9 August 2011). Plant Systematics. Amsterdam: Elsevier. ISBN 9780080514048.
  15. Russell PJ, Hertz PE, McMillan B (2013). Biology: The Dynamic Science. Cengage Learning. ISBN 978-1-285-41534-5.
  16. Lipscomb D (1998). "Basics of Cladistic Analysis" (PDF). Washington D.C.: George Washington University.
  17. Choudhuri S (2014-05-09). Bioinformatics for Beginners: Genes, Genomes, Molecular Evolution, Databases and Analytical Tools (1st ed.). Academic Press. p. 51. ISBN 978-0-12-410471-6. OCLC 950546876.
  18. Williams D, Schmitt M, Wheeler Q (2016-07-21). The Future of Phylogenetic Systematics: The Legacy of Willi Hennig. ISBN 978-1-107-11764-8. OCLC 951563305.
  19. Avise JC, Robinson TJ (June 2008). "Hemiplasy: a new term in the lexicon of phylogenetics". Systematic Biology. 57 (3): 503–7. doi:10.1080/10635150802164587. PMID 18570042.
  20. Copetti D, Búrquez A, Bustamante E, Charboneau JL, Childs KL, Eguiarte LE, et al. (November 2017). "Extensive gene tree discordance and hemiplasy shaped the genomes of North American columnar cacti". Proceedings of the National Academy of Sciences of the United States of America. 114 (45): 12003–12008. doi:10.1073/pnas.1706367114. PMC 5692538. PMID 29078296.
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