In
biology
Biology is the scientific study of life. It is a natural science with a broad scope but has several unifying themes that tie it together as a single, coherent field. For instance, all organisms are made up of cells that process hereditar ...
, phylogenetics (; from
Greek φυλή/
φῦλον [] "tribe, clan, race", and wikt:γενετικός, γενετικός [] "origin, source, birth") is the study of the evolutionary history and relationships among or within groups of organisms. These relationships are determined by
Computational phylogenetics, phylogenetic inference methods that focus on observed
heritable traits, such as
DNA sequences,
protein
Proteins are large biomolecules and macromolecules that comprise one or more long chains of amino acid residues. Proteins perform a vast array of functions within organisms, including catalysing metabolic reactions, DNA replication, respon ...
amino acid
Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. Although hundreds of amino acids exist in nature, by far the most important are the alpha-amino acids, which comprise proteins. Only 22 alpha ...
sequences, or
morphology. The result of such an analysis is a
phylogenetic tree
A phylogenetic tree (also phylogeny or evolutionary tree Felsenstein J. (2004). ''Inferring Phylogenies'' Sinauer Associates: Sunderland, MA.) is a branching diagram or a tree showing the evolutionary relationships among various biological spec ...
—a diagram containing a hypothesis of relationships that reflects the evolutionary history of a group of organisms.
The tips of a phylogenetic tree can be living taxa or fossils, and represent the "end" or the present time in an evolutionary lineage. A phylogenetic diagram can be rooted or unrooted. A rooted tree diagram indicates the hypothetical common ancestor of the tree. An unrooted tree diagram (a network) makes no assumption about the ancestral line, and does not show the origin or "root" of the taxa in question or the direction of inferred evolutionary transformations.
In addition to their use for inferring phylogenetic patterns among taxa, phylogenetic analyses are often employed to represent relationships among genes or individual organisms. Such uses have become central to understanding biodiversity, evolution, ecology, and genomes.
Phylogenetics is part of
systematics
Biological systematics is the study of the diversification of living forms, both past and present, and the relationships among living things through time. Relationships are visualized as evolutionary trees (synonyms: cladograms, phylogenetic tre ...
.
Taxonomy is the identification, naming and
classification of organisms. Classifications are now usually based on phylogenetic data, and many systematists contend that only
monophyletic
In cladistics for a group of organisms, monophyly is the condition of being a clade—that is, a group of taxa composed only of a common ancestor (or more precisely an ancestral population) and all of its lineal descendants. Monophyletic gro ...
taxa should be recognized as named groups. The degree to which classification depends on inferred evolutionary history differs depending on the school of taxonomy:
phenetics ignores phylogenetic speculation altogether, trying to represent the similarity between organisms instead;
cladistics (phylogenetic systematics) tries to reflect phylogeny in its classifications by only recognizing groups based on shared, derived characters (
synapomorphies
In phylogenetics, an apomorphy (or derived trait) is a novel character or character state that has evolved from its ancestral form (or plesiomorphy). A synapomorphy is an apomorphy shared by two or more taxa and is therefore hypothesized to have ...
);
evolutionary taxonomy tries to take into account both the branching pattern and "degree of difference" to find a compromise between them.
Inference of a phylogenetic tree
Usual methods of
phylogenetic inference involve computational approaches implementing the
optimality criteria and methods of
parsimony
Parsimony refers to the quality of economy or frugality in the use of resources.
Parsimony may also refer to
* The Law of Parsimony, or Occam's razor, a problem-solving principle
** Maximum parsimony (phylogenetics), an optimality criterion in p ...
,
maximum likelihood (ML), and
MCMC-based
Bayesian inference. All these depend upon an implicit or explicit
mathematical model
A mathematical model is a description of a system using mathematical concepts and language. The process of developing a mathematical model is termed mathematical modeling. Mathematical models are used in the natural sciences (such as physics, ...
describing the evolution of characters observed.
Phenetics, popular in the mid-20th century but now largely obsolete, used
distance matrix
In mathematics, computer science and especially graph theory, a distance matrix is a square matrix
In mathematics, a square matrix is a matrix with the same number of rows and columns. An ''n''-by-''n'' matrix is known as a square matrix of orde ...
-based methods to construct trees based on overall similarity in
morphology or similar observable traits (i.e. in the
phenotype or the
overall similarity of DNA, not the
DNA sequence), which was often assumed to approximate phylogenetic relationships.
Prior to 1950, phylogenetic inferences were generally presented as
narrative
A narrative, story, or tale is any account of a series of related events or experiences, whether nonfictional ( memoir, biography, news report, documentary, travelogue, etc.) or fictional (fairy tale, fable, legend, thriller
Thriller may r ...
scenarios. Such methods are often ambiguous and lack explicit criteria for evaluating alternative hypotheses.
History
The term "phylogeny" derives from the German , introduced by Haeckel in 1866, and the
Darwinian approach to classification became known as the "phyletic" approach.
Ernst Haeckel's recapitulation theory
During the late 19th century,
Ernst Haeckel's
recapitulation theory, or "biogenetic fundamental law", was widely accepted. It was often expressed as "
ontogeny recapitulates phylogeny", i.e. the development of a single organism during its lifetime, from germ to adult, successively mirrors the adult stages of successive ancestors of the species to which it belongs. But this theory has long been rejected. Instead,
ontogeny evolves – the phylogenetic history of a species cannot be read directly from its ontogeny, as Haeckel thought would be possible, but characters from ontogeny can be (and have been) used as data for phylogenetic analyses; the more closely related two species are, the more
apomorphies their embryos share.
Timeline of key points
*14th century, ''lex parsimoniae'' (parsimony principle),
William of Ockam, English philosopher, theologian, and Franciscan friar, but the idea actually goes back to
Aristotle
Aristotle (; grc-gre, Ἀριστοτέλης ''Aristotélēs'', ; 384–322 BC) was a Greek philosopher and polymath during the Classical Greece, Classical period in Ancient Greece. Taught by Plato, he was the founder of the Peripatet ...
, precursor concept
*1763, Bayesian probability, Rev. Thomas Bayes, precursor concept
*18th century, Pierre Simon (Marquis de Laplace), perhaps first to use ML (maximum likelihood), precursor concept
*1809, evolutionary theory, ''
Philosophie Zoologique
''Philosophie zoologique'' ("Zoological Philosophy, or Exposition with Regard to the Natural History of Animals") is an 1809 book by the French naturalist Jean-Baptiste Lamarck, in which he outlines his pre-Darwinian theory of evolution, part of ...
,''
Jean-Baptiste de Lamarck, precursor concept, foreshadowed in the 17th century and 18th century by Voltaire, Descartes, and Leibniz, with Leibniz even proposing evolutionary changes to account for observed gaps suggesting that many species had become extinct, others transformed, and different species that share common traits may have at one time been a single race, also foreshadowed by some early Greek philosophers such as
Anaximander in the 6th century BC and the atomists of the 5th century BC, who proposed rudimentary theories of evolution
*1837, Darwin's notebooks show an evolutionary tree
*1843, distinction between
homology and
analogy (the latter now referred to as
homoplasy), Richard Owen, precursor concept
*1858, Paleontologist Heinrich Georg Bronn (1800–1862) published a hypothetical tree to illustrating the paleontological "arrival" of new, similar species following the extinction of an older species. Bronn did not propose a mechanism responsible for such phenomena, precursor concept.
*1858, elaboration of evolutionary theory, Darwin and Wallace, also in Origin of Species by Darwin the following year, precursor concept
*1866,
Ernst Haeckel, first publishes his phylogeny-based evolutionary tree, precursor concept
*1893, Dollo's Law of Character State Irreversibility, precursor concept
*1912, ML recommended, analyzed, and popularized by Ronald Fisher, precursor concept
*1921, Tillyard uses term "phylogenetic" and distinguishes between archaic and specialized characters in his classification system
*1940, term "
clade" coined by Lucien Cuénot
*1949,
Jackknife resampling, Maurice Quenouille (foreshadowed in '46 by Mahalanobis and extended in '58 by Tukey), precursor concept
*1950, Willi Hennig's classic formalization
*1952, William Wagner's groundplan divergence method
*1953, "cladogenesis" coined
*1960, "cladistic" coined by Cain and Harrison
*1963, first attempt to use ML (maximum likelihood) for phylogenetics, Edwards and Cavalli-Sforza
*1965
**Camin-Sokal parsimony, first parsimony (optimization) criterion and first computer program/algorithm for cladistic analysis both by Camin and Sokal
**character compatibility method, also called clique analysis, introduced independently by Camin and Sokal (loc. cit.) and
E. O. Wilson
*1966
**English translation of Hennig
**"cladistics" and "cladogram" coined (Webster's, loc. cit.)
*1969
**dynamic and successive weighting, James Farris
**Wagner parsimony, Kluge and Farris
**CI (consistency index), Kluge and Farris
**introduction of pairwise compatibility for clique analysis, Le Quesne
*1970, Wagner parsimony generalized by Farris
*1971
**first successful application of ML to phylogenetics (for protein sequences), Neyman
**Fitch parsimony, Fitch
**NNI (nearest neighbour interchange), first branch-swapping search strategy, developed independently by Robinson and Moore et al.
**ME (minimum evolution), Kidd and Sgaramella-Zonta (it is unclear if this is the pairwise distance method or related to ML as Edwards and Cavalli-Sforza call ML "minimum evolution")
*1972, Adams consensus, Adams
*1976, prefix system for ranks, Farris
*1977, Dollo parsimony, Farris
*1979
**Nelson consensus, Nelson
**MAST (maximum agreement subtree)((GAS)greatest agreement subtree), a consensus method, Gordon
**bootstrap, Bradley Efron, precursor concept
*1980, PHYLIP, first software package for phylogenetic analysis, Felsenstein
*1981
**majority consensus, Margush and MacMorris
**strict consensus, Sokal and Rohlf
**first computationally efficient ML algorithm, Felsenstein
*1982
**PHYSIS, Mikevich and Farris
**branch and bound, Hendy and Penny
*1985
**first cladistic analysis of eukaryotes based on combined phenotypic and genotypic evidence Diana Lipscomb
**first issue of ''Cladistics''
**first phylogenetic application of bootstrap, Felsenstein
**first phylogenetic application of jackknife, Scott Lanyon
*1986, MacClade, Maddison and Maddison
*1987, neighbor-joining method Saitou and Nei
*1988, Hennig86 (version 1.5), Farris
**Bremer support (decay index), Bremer
*1989
**RI (retention index), RCI (rescaled consistency index), Farris
**HER (homoplasy excess ratio), Archie
*1990
**combinable components (semi-strict) consensus, Bremer
**SPR (subtree pruning and regrafting), TBR (tree bisection and reconnection), Swofford and Olsen
*1991
**DDI (data decisiveness index), Goloboff
**first cladistic analysis of eukaryotes based only on phenotypic evidence, Lipscomb
*1993, implied weighting Goloboff
*1994, reduced consensus: RCC (reduced cladistic consensus) for rooted trees, Wilkinson
*1995, reduced consensus RPC (reduced partition consensus) for unrooted trees, Wilkinson
*1996, first working methods for BI (Bayesian Inference)independently developed by Li, Mau, and Rannala and Yang and all using MCMC (Markov chain-Monte Carlo)
*1998, TNT (Tree Analysis Using New Technology), Goloboff, Farris, and Nixon
*1999, Winclada, Nixon
*2003, symmetrical resampling, Goloboff
*2004,2005, symmilarity metric (using an approximation to Kolmogorov complexity) or NCD (normalized compression distance), Li et al., Cilibrasi and Vitanyi.
Outside biology
Phylogenetic tools and representations (trees and networks) can also be applied to studying the evolution of languages, in the field of
quantitative comparative linguistics.
See also
*
Angiosperm Phylogeny Group
*
Bauplan
*
Bioinformatics
*
Biomathematics
*
Coalescent theory
*
EDGE of Existence programme
*
Evolutionary taxonomy
*
Language family
*
Maximum parsimony
*
Microbial phylogenetics
*
Molecular phylogeny
*
Noogenesis
*
Ontogeny
*
PhyloCode
*
Phylodynamics
*
Phylogenesis
*
Phylogenetic comparative methods
*
Phylogenetic network
*
Phylogenetic nomenclature
Phylogenetic nomenclature is a method of nomenclature for taxa in biology that uses phylogenetic definitions for taxon names as explained below. This contrasts with the traditional approach, in which taxon names are defined by a ''type'', whic ...
*
Phylogenetic tree viewers
*
Phylogenetics software
*
Phylogenomics
Phylogenomics is the intersection of the fields of evolution and genomics. The term has been used in multiple ways to refer to analysis that involves genome data and evolutionary reconstructions. It is a group of techniques within the larger fields ...
*
Phylogeny (psychoanalysis)
*
Phylogeography
*
Systematics
Biological systematics is the study of the diversification of living forms, both past and present, and the relationships among living things through time. Relationships are visualized as evolutionary trees (synonyms: cladograms, phylogenetic tre ...
References
Bibliography
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External links
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