Jump to content

Polyphyly

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Mrjulesd (talk | contribs) at 12:25, 9 July 2020 (c/e). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

In this phylogenetic tree, the blue and red groups (which are both monophyletic) do not share an immediate common ancestor; if they both share characteristics that appear to be similar, the blue and red groups form a polyphyletic group.
Cladogram of the primates, showing a monophyly (the simians, in yellow), a paraphyly (the prosimians, in cyan, including the red patch), and a polyphyly (the night-active primates, the lorises and the tarsiers, in red).
Phylogenetic groups: A monophyletic taxon (in yellow, the clade Sauropsida grouping "reptiles and birds") contains a common ancestor and all of its descendants. A paraphyletic taxon (in cyan, the "reptiles") contains its most recent common ancestor, but does not contain all the descendants of that ancestor. A polyphyletic taxon (in red, the group Haemothermia containing warm-blooded tetrapods) does not contain the most recent common ancestor of all its members.

A polyphyletic group is a set of organisms, or other evolving elements, that have been grouped together but do not share an immediate common ancestor. The term is often applied to groups that share characteristics that appear to be similar but have not been inherited from common ancestors; these characteristics are known as homoplasies, and the development and phenomenon of homoplasies is known as convergent evolution. The arrangement of the members of a polyphyletic group is called a polyphyly.

Alternatively, polyphyletic is simply used to describe a group whose members come from multiple ancestral sources, regardless of similarity of characteristics. For example, the biological characteristic of warm-bloodedness evolved separately in the ancestors of mammals and the ancestors of birds.[1] Other polyphyletic groups are for example algae, C4 photosynthetic plants,[2] and edentates.[3]

Many biologists aim to avoid homoplasies in grouping taxa together and therefore it is frequently a goal to eliminate groups that are found to be polyphyletic. This is often the stimulus for major revisions of the classification schemes.

Researchers concerned more with ecology than with systematics may take polyphyletic groups as legitimate subject matter; the similarities in activity within the fungus group Alternaria, for example, can lead researchers to regard the group as a valid genus while acknowledging its polyphyly.[4]. In recent research, the concepts of monophyly, paraphyly, and polyphyly have been used in deducing key genes for barcoding of diverse group of species.[5]

Etymology

The term polyphyly, or polyphyletic, derives from the two ancient greek words πολύς (polús), meaning "many, a lot of", and φῦλον (phûlon), meaning "genus, species",[6][7] and refers to the fact that a polyphyletic group includes organisms (e.g., genera, species) arising from multiple ancestral sources.

Conversely, the term monophyly, or monophyletic, builds on the ancient greek prefix μόνος (mónos), meaning "alone, only, unique",[6][7] and refers to the fact that a monophyletic group includes organisms consisting of all the descendants of a unique common ancestor.

By comparison, the term paraphyly, or paraphyletic, uses the ancient greek prefix παρά (pará), meaning "beside, near",[6][7] and refers to the situation in which one or several monophyletic subgroups are left apart from all other descendants of a unique common ancestor.

Avoidance

In many schools of taxonomy, the existence of polyphyletic groups in a classification is discouraged. Monophyletic groups (that is, clades) are considered by these schools of thought to be the most important grouping of organisms.

One reason for this view is that some clades are simple to define in purely phylogenetic terms without reference to clades previously introduced: a node-based clade definition, for example, could be "All descendants of the last common ancestor of species X and Y". On the other hand, polyphyletic groups can often be delimited in terms of clades, for example "the flying vertebrates consist of the bat, bird, and pterosaur clades". Because polyphyletic groups can frequently be defined as a sum of clades, they are usually considered less fundamental than monophyletic (single, whole) clades.

A stronger reason is that grouping species monophyletically facilitates prediction far more than does polyphyletic grouping. For example, classifying a newly discovered grass in the monophyletic family Poaceae, the true grasses, immediately results in numerous predictions about its structure and its developmental and reproductive characteristics, inherited from the common ancestor of this family. In contrast, Linnaeus' assignment of plants with two stamens to the polyphyletic class Diandria, while practical for identification, turns out to be useless for prediction, since the presence of exactly two stamens has developed convergently in many groups.[8] Predictive success is the touchstone by which theories are evaluated in all experimental sciences.

Polyphyletic species

Species have a special status in systematics as being an observable feature of nature itself and as the basic unit of classification.[9] It is usually implicitly assumed that species are monophyletic (or at least paraphyletic). However hybrid speciation arguably leads to polyphyletic species.[10] Hybrid species are a common phenomenon in nature, particularly in plants where polyploidy allows for rapid speciation.[11]

See also

Notes

  1. ^ Archibald, J. David (2014-07-15). Aristotle's Ladder, Darwin's Tree: The Evolution of Visual Metaphors for Biological Order. Columbia University Press. ISBN 9780231164122.
  2. ^ Sage, Rowan F. (2004-02-01). "The evolution of C4 photosynthesis". New Phytologist. 161 (2): 341–370. doi:10.1111/j.1469-8137.2004.00974.x. ISSN 1469-8137.
  3. ^ Delsuc, Frédéric; Douzery, Emmanuel J. P. (2008). "Recent advances and future prospects in xenarthran molecular phylogenetics". In Vizcaíno, Sergio F.; Loughry, W. J. (eds.). The biology of the Xenarthra. Gainesville: University Press of Florida. pp. 11–23. ISBN 9780813031651. OCLC 741613153.
  4. ^ Aschehoug, Erik T.; Metlen, Kerry L.; Callaway, Ragan M.; Newcombe, George (2012). "Fungal endophytes directly increase the competitive effects of an invasive forb" (PDF). Ecology. 93 (1): 3–8. doi:10.1890/11-1347.1. PMID 22486080. Archived from the original (PDF) on April 28, 2014. Retrieved July 8, 2013.
  5. ^ Parhi J., Tripathy P.S., Priyadarshi, H., Mandal S.C., Pandey P.K. (2019). "Diagnosis of mitogenome for robust phylogeny: A case of Cypriniformes fish group". Gene. 713: 143967. doi:10.1016/j.gene.2019.143967. PMID 31279710.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  6. ^ a b c Bailly, Anatole (1981-01-01). Abrégé du dictionnaire grec français. Paris: Hachette. ISBN 978-2010035289. OCLC 461974285.
  7. ^ a b c Bailly, Anatole. "Greek-french dictionary online". www.tabularium.be. Retrieved March 2, 2018.
  8. ^ Stace, Clive A. (2010). "Classification by molecules: What's in it for field botanists?" (PDF). Watsonia. 28: 103–122. Archived from the original (PDF) on October 15, 2012. Retrieved July 31, 2013.
  9. ^ Queiroz, Kevin; Donoghue, Michael J. (December 1988). "Phylogenetic Systematics and the Species Problem". Cladistics. 4 (4): 317–338. doi:10.1111/j.1096-0031.1988.tb00518.x.
  10. ^ Hörandl, E.; Stuessy, T.F. (2010). "Paraphyletic groups as natural units of biological classification". Taxon. 59 (6): 1641–1653. doi:10.1002/tax.596001.
  11. ^ Linder, C.R.; Risenberg, L.H. (22 June 2004). "Reconstructing patterns of reticulate evolution in plants". American Journal of Botany. 91 (10): 1700–1708. doi:10.3732/ajb.91.10.1700. PMC 2493047. PMID 18677414. Retrieved 14 December 2011.

References