Xenarthra

Xenarthra
Temporal range: Middle Paleocene - Recent
Hoffmann's Two-toed Sloth
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Mammalia
Subclass: Theriiformes
Infraclass: Eutheria
Superorder: Xenarthra
Cope, 1889
Orders and suborders

See text for more details

The superorder Xenarthra is a group of placental mammals (infraclass Eutheria), extant today only in the Americas and represented by anteaters, tree sloths, and armadillos. The origins of the order can be traced back as far as the Paleogene (about 60-65 Ma, shortly after the Mesozoic) in South America[1] . Xenarthrans developed and diversified extensively in South America during its long period of isolation, invaded the Antilles by the early Miocene, and then spread to Central and North America starting about nine million years ago, as part of the Great American Interchange[2] . Nearly all of the formerly abundant megafaunal xenarthrans, such as ground sloths, glyptodonts, and pampatheres went extinct at the end of the Pleistocene.

Xenarthrans share several distinctions from those of other placental mammals. The name Xenarthra means "strange joints", and was chosen because their vertebral joints have extra articulations and are unlike those of any other mammals. The males lack external testicles, which are instead placed between the bladder and the rectum[3]. Also, xenarthrans have the lowest metabolic rates among the therians.[4][5]

Contents

Evolutionary relationships

Xenarthrans were classified in the past together with the pangolins and aardvarks as the order Edentata (meaning toothless, because the members do not have front incisor teeth or molars, or have poorly-developed molars). It was subsequently realized that Edentata was polyphyletic—that it contained unrelated families and was subsequently split up to reflect their true phylogeny. Aardvarks and pangolins are now placed in individual orders, and the new order Xenarthra was erected to group the remaining families (which are all related). The name Xenarthra means "strange joints", and was chosen because their vertebral joints have extra articulations and are unlike those of any other mammals. Because they lack characteristics believed to be present in the common ancestor of other known eutherian mammals, some weak morphological evidence suggests that the Xenarthra are outside the Epitheria, which contains all other known eutherians today. Some workers have even placed xenarthrans outside of placentals as a separate group Paratheria.[6]

The morphology of xenarthrans generally suggests that the anteaters and sloths are closest together within Xenarthra, which is upheld by molecular studies. The order Xenarthra is more and more often divided into two orders: Pilosa, containing the Vermilingua (anteaters) and Folivora (sloths; previously known as Tardigrada or Phyllophaga), and the separate order Cingulata (armadillos). Xenarthra now has the rank of cohort or super-order. The Xenarthra are part of the super-cohort Atlantogenata.

Xenarthra may be most closely related to either Afrotheria[7] (in the group Atlantogenata), or Epitheria[8] (comprising Afrotheria and Boreoeutheria). In other words it may be nested within Eutheria or it may be the basal extant group. A comprehensive phylogeny by Goloboff et al.[9] includes xenarthrans as a sister clade of Boreoeutheria (Euarchontoglires+Laurasiatheria) (in the Exafroplacentalia=Notolegia).

Classification

SUPERORDER XENARTHRA

References

  1. ^ Archibald, J. David (August 2003). "Timing and biogeography of the eutherian radiation: fossils and molecules compared". Molecular Phylogenetics and Evolution 28: 350–359. PMID 12878471. http://www.ncbi.nlm.nih.gov/pubmed/12878471. 
  2. ^ Woodburne, Michael (2010). "The Great American Biotic Interchange: Dispersals, Tectonics, Climate, Sea Level, and Holding Pens". Journal of Mammalian Evolution 17 (4): 245–264. doi:10.1007/s10914-010-9144-8Open Access. http://www.springerlink.com/content/35576417v5723n02/. Retrieved 18 October 2011. 
  3. ^ Kleisner, Karel; Richard Ivell, Jaroslav Flegr (March 2010). "The evolutionary history of testicular externalization and the origin of the scrotum". J. Biosc. 35 (1): 27–37. PMID 20413907. http://www.ncbi.nlm.nih.gov/pubmed/20413907. 
  4. ^ Elgar, M. A.; Harvey, P. H. (1987). "Basal Metabolic Rates in Mammals: Allometry, Phylogeny and Ecology". Functional Ecology (British Ecological Society) 1 (1): 25–36. doi:10.2307/2389354. JSTOR 2389354. 
  5. ^ Lovegrove, B. G. (2000-08). "The Zoogeography of Mammalian Basal Metabolic Rate". The American Naturalist (The University of Chicago Press) 156 (2): 201–219. doi:10.1086/303383. JSTOR 3079219. PMID 10856202. 
  6. ^ Gaudin, T.J.; Wible, J.R.; Hopson, J.A.; Turnbull, W.D. (1996). "Reexamination of the morphological evidence for the cohort Epitheria (Mammalia, Eutheria)". Journal of Mammalian Evolution 3: 31–79. doi:10.1007/BF01454253.  edit
  7. ^ Murphy, W.J., Pringle, T.H., Crider, T.A., Springer, M.S. & Miller, W. 2007. Using genomic data to unravel the root of the placental mammal phylogeny. Genome Research 17, pp.413-421.
  8. ^ Kriegs, J.O., Churakov, G., Kiefmann, M., Jordan, U., Brosius, J. & Schmitz, J. 2006. Retroposed elements as archives for the evolutionary history of placental mammals. Plos Biol 4, pp.e91.
  9. ^ Goloboff, P.A.; Catalano, S.A.; Mirande, J.M.; Szumik, C.A.; Arias, J.S.; Källersjö, M & Farris, J.S. 2009. Phylogenetic analysis of 73 060 taxa corroborates major eukaryotic groups. Cladistics 25 (3): 211-230

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