Evolutionary grade explained

A grade is a taxon united by a level of morphological or physiological complexity. The term was coined by British biologist Julian Huxley, to contrast with clade, a strictly phylogenetic unit.[1]

Phylogenetics

In order to fully understand evolutionary grades, one must first get a better understanding of phylogenetics: the study of the evolutionary history and relationships among or within groups of organisms. These relationships are determined by phylogenetic inference methods that focus on observed heritable traits, such as DNA sequences, protein amino acid sequences, or morphology. The result of such an analysis is a phylogenetic tree—a diagram containing a hypothesis of relationships that reflects the evolutionary history of a group of organisms.[2]

Definition of an evolutionary grade

An evolutionary grade is a group of species united by morphological or physiological traits, that has given rise to another group that has major differences from the ancestral group's condition, and is thus not considered part of the ancestral group, while still having enough similarities that we can group them under the same clade. The ancestral group will not be phylogenetically complete (i.e. is not a clade), and so will represent a paraphyletic taxon.

The most commonly cited example is that of reptiles. In the early 19th century, the French naturalist Latreille was the first to divide tetrapods into the four familiar classes of amphibians, reptiles, birds, and mammals.[3] In this system, reptiles are characterized by traits such as laying membranous or shelled eggs, having skin covered in scales or scutes, and having a 'cold-blooded' metabolism. However, the ancestors of mammals and birds also had these traits and so birds and mammals can be said to "have evolved from reptiles", making the reptiles, when defined by these traits, a grade rather than a clade. In microbiology, taxa that are thus seen as excluded from their evolutionary grade parent group are called taxa in disguise.[4]

Paraphyletic taxa will often, but not always, represent evolutionary grades. In some cases paraphyletic taxa are united simply by not being part of any other groups, and give rise to so-called wastebasket taxa which may even be polyphyletic.

Grades in systematics

The traditional Linnaean way of defining taxa is through the use of anatomical traits. When the actual phylogenetic relationship is unknown, well defined groups sometimes turn out to be defined by traits that are primitive rather than derived. In Linnaean systematics, evolutionary grades are accepted in higher taxonomic ranks, though generally avoided at family level and below. In phylogenetic nomenclature evolutionary grades (or any other form of paraphyly) are not accepted.[5]

Where information about phylogenetic relationships is available, organisms are preferentially grouped into clades. Where data is lacking, or groups of uncertain relationship are to be compared, the cladistic method is limited and grade provides a useful tool for comparing organisms. This is particularly common in palaeontology, where fossils are often fragmentary and difficult to interpret. Thus, traditional palaeontological works are often using evolutionary grades as formal or informal taxa, including examples such as labyrinthodonts, anapsids, synapsids, dinosaurs, ammonites, eurypterids, lobopodians and many of the more well known taxa of human evolution. Organizing organisms into grades rather than strict clades can also be very useful to understand the evolutionary sequence behind major diversification of both animals[6] and plants.[7]

Evolutionary grades, being united by gross morphological traits, are often eminently recognizable in the field. While taxonomy seeks to eliminate paraphyletic taxa, such grades are sometimes kept as formal or informal groups on the basis of their usefulness for laymen and field researchers.[5] In bacteriology, the renaming of species or groups that turn out to be evolutionary grades is kept to a minimum to avoid misunderstanding, which in the case of pathogens could have fatal consequences. When referring to a group of organisms, the term "grade" is usually enclosed in quotation marks to denote its status as a paraphyletic term.

Grades and phylogenetic nomenclature

With the rise of phylogenetic nomenclature, the use of evolutionary grades as formal taxa has come under debate. Under a strict phylogenetic approach, only monophyletic taxa are recognized.[8] This differs from the more traditional approach of evolutionary taxonomy.[9] The difference in approach has led to a vigorous debate between proponents of the two approaches to taxonomy, particularly in well established fields like vertebrate palaeontology and botany.[10] The difference between the statement "B is part of A" (phylogenetic approach) and "B has evolved from A" (evolutionary approach) is, however, one of semantics rather than of phylogeny. Both express the same phylogeny, but the former emphasizes the phylogenetic continuum while the latter emphasizes a distinct shift in anatomy or ecology in B relative to A.

Examples

Notes and References

  1. Huxley J. 1959. Clades and grades. In Cain A.J. (ed) Function and taxonomic importance. Systematics Association, London.
  2. Web site: phylogeny. Biology online. 2013-02-15.
  3. Latreille, P.A. (1804). Nouveau Dictionnaire à Histoire Naturelle, xxiv; cited in Latreille, P.A. (1825).Familles naturelles du règne animal, exposés succinctement et dans un ordre analytique.
  4. Lan . R . Reeves . PR . Escherichia coli in disguise: molecular origins of Shigella . Microbes and Infection / Institut Pasteur . 4 . 11 . 1125–32 . 2002 . 12361912. 10.1016/S1286-4579(02)01637-4.
  5. 10.2307/2446408 . Primary Classification and Phylogeny of the Polemoniaceae, with Comments on Molecular Cladistics . 1998 . Grant, Verne . American Journal of Botany . 85 . 741–752 . 2446408 . 6 . 21684957 . free .
  6. Sperling. E. A.. Pisani, D.. Peterson, K. J.. Poriferan paraphyly and its implications for Precambrian palaeobiology. Geological Society, London, Special Publications. 1 January 2007. 286. 1. 355–368. 10.1144/SP286.25. 22 August 2012. 2007GSLSP.286..355S. 34175521. dead. https://web.archive.org/web/20090509061759/http://www.dartmouth.edu/~peterson/Sperling,%20Pisani%20and%20Peterson.pdf. 9 May 2009. dmy-all.
  7. Donoghue. Michael J.. Key innovations, convergence, and success: macroevolutionary lessons from plant phylogeny. Paleobiology. 1 June 2005. 31. sp5. 77–93. 10.1666/0094-8373(2005)031[0077:KICASM]2.0.CO;2. 36988476 .
  8. Kevin de Queiroz & Jacques Gauthier . 1990 . Phylogeny as a central principle in taxonomy: phylogenetic definitions of taxon names . Syst. Zool. . 39 . 307–322 . 10.2307/2992353 . 2992353 . 4.
  9. Mayr . Ernst . Ernst W. Mayr . Bock . W.J. . 2002 . Classifications and other ordering systems . J. Zool. Syst. Evol. Research . 40 . 4 . 169–94 . 10.1046/j.1439-0469.2002.00211.x . amp .
  10. Benton. M. J.. 2000. Stems, nodes, crown clades, and rank-free lists: is Linnaeus dead?. Biological Reviews. 0006-3231. 75. 4. 633–648. 10.1111/j.1469-185X.2000.tb00055.x. 11117201. dead. https://web.archive.org/web/20110605090428/http://palaeo.gly.bris.ac.uk/Essays/phylocode/biolrev.html. 5 June 2011. dmy-all. 10.1.1.573.4518. 17851383.
  11. [Alfred Romer|Romer, A.S]
  12. Huxley . Thomas H. . Further Evidence of the Affinity between the Dinosaurian Reptiles and Birds . Quarterly Journal of the Geological Society of London/Volume 26/Further Evidence of the Affinity between the Dinosaurian Reptiles and Birds . Quarterly Journal of the Geological Society of London . 26 . 1870 . 10.1144/GSL.JGS.1870.026.01-02.08 . 12–31 . yes . yes .
  13. Book: Gibbons . J. Whitfield . Gibbons . Whit . Their Blood Runs Cold: Adventures With Reptiles and Amphibians . registration . University of Alabama Press . 1983 . . 164 . 978-0-8173-0135-4 .