Cingulata Explained

Cingulata, part of the superorder Xenarthra, is an order of armored New World placental mammals. Dasypodids and chlamyphorids, the armadillos, are the only surviving families in the order. Two groups of cingulates much larger than extant armadillos (maximum body mass of 45 kg (100 lb) in the case of the giant armadillo[1]) existed until recently: pampatheriids, which reached weights of up to 200 kg (440 lb)[2] and chlamyphorid glyptodonts, which attained masses of 2,000 kg (4,400 lb)[3] or more.

The cingulate order originated in South America during the Paleocene epoch about 66 to 56 million years ago, and due to the continent's former isolation remained confined to it during most of the Cenozoic. However, the formation of a land bridge allowed members of all three families to migrate to southern North America during the Pliocene[4] or early Pleistocene[5] as part of the Great American Interchange. After surviving for tens of millions of years, all of the pampatheriids and giant glyptodonts apparently died out during the Quaternary extinction event at the beginning of the Holocene,[6] [7] along with much of the rest of the regional megafauna, shortly after the colonization of the Americas by Paleo-Indians.

Description

Armadillos have dorsal armor that is formed by osteoderms, plates of dermal bone covered in relatively small, overlapping keratinized epidermal scales called "scutes". Most species have rigid shields over the shoulders and hips, with three to nine bands separated by flexible skin covering the back and flanks.[8]

Pampatheres also had shells that were flexible due to three movable lateral bands of osteoderms.[2] The osteoderms of pampatheres were each covered by a single scute, unlike those of armadillos, which have more than one.[2] Glyptodonts, on the other hand, had rigid, turtle-like shells of fused osteoderms.

Both groups have or had a cap of armor atop their heads. Glyptodonts also had heavily armored tails; some, such as Doedicurus, had mace-like clubs at the ends of their tails, similar to those of ankylosaurs, evidently used for defensive or agonistic purposes.

Most armadillos eat insects and other invertebrates; some are more omnivorous and may also eat small vertebrates and vegetable matter. Pampatheres are thought to have been specialized for grazing,[2] and isotopic analysis indicates the diet of glyptodonts was dominated by C4 grasses.[9] Euphractinae is unique for speciations towards carnivory, culminating in the macropredatory genus Macroeuphractus.

Classification

See main article: List of cingulates.

The taxonomic table below follows the results of a phylogenetic analysis published by Delsuc et al., 2016. While glyptodonts have traditionally been considered stem-group cingulates outside the group that contains modern armadillos, this 2016 study conducted an analysis of Doedicurus mtDNA and found that it was, in fact, nested within the modern armadillos as the sister group of a clade consisting of Chlamyphorinae and Tolypeutinae.

Order Cingulata

Notes and References

  1. http://www.faunaparaguay.com/mamm6Priodontesmaximus.pdf Giant Armadillo Priodontes maximus (Kerr, 1792)
  2. Vizcaíno . S. F. . De Iuliis, G. . Bargo, M. S. . Skull Shape, Masticatory Apparatus, and Diet of Vassallia and Holmesina (Mammalia: Xenarthra: Pampatheriidae): When Anatomy Constrains Destiny . Journal of Mammalian Evolution . 5 . 4 . 291–322 . 1998 . 10.1023/A:1020500127041 . 20186439 .
  3. Blanco. R. E.. Jones. W. W.. Rinderknecht. A.. The sweet spot of a biological hammer: the centre of percussion of glyptodont (Mammalia: Xenarthra) tail clubs. Proceedings of the Royal Society B: Biological Sciences. 276. 1675. 2009-08-26. 3971–3978. 0962-8452. 10.1098/rspb.2009.1144. 19710060. 2825778.
  4. Mead . J. I. . Swift, S. L. . White, R. S. . McDonald, H. G. . Baez, A. . Late Pleistocene (Rancholabrean) Glyptodont and Pampathere (Xenarthra, Cingulata) from Sonora, Mexico . . 24 . 3 . 439–449 (see p. 440) . 2007 . 2013-06-15.
  5. Woodburne. M. O.. The Great American Biotic Interchange: Dispersals, Tectonics, Climate, Sea Level and Holding Pens. Journal of Mammalian Evolution. 17. 4. 2010-07-14. 245–264 (see p. 249). 1064-7554. 10.1007/s10914-010-9144-8. 21125025. 2987556.
  6. Hubbe. A.. Hubbe. M.. Neves. W. A.. The Brazilian megamastofauna of the Pleistocene/Holocene transition and its relationship with the early human settlement of the continent. Earth-Science Reviews. 118. March 2013. 1–10 (see pages 3, 6). 0012-8252. 10.1016/j.earscirev.2013.01.003. 2013ESRv..118....1H.
  7. Book: Fiedal, Stuart . Haynes . Gary . Sudden Deaths: The Chronology of Terminal Pleistocene Megafaunal Extinction . American Megafaunal Extinctions at the End of the Pleistocene . 2009 . 21–37 (see p. 31). . 10.1007/978-1-4020-8793-6_2 . 978-1-4020-8792-9 . 313368423. Vertebrate Paleobiology and Paleoanthropology .
  8. Book: Macdonald, D. . Dickman, Christopher R. . 1984 . The Encyclopedia of Mammals . Facts on File . New York . 781–783 . 978-0-87196-871-5 . registration .
  9. Pérez-Crespo. V. A.. Arroyo-Cabrales. J.. Alva-Valdivia. L. M.. Morales-Puente. P.. Cienfuegos-Alvarado. E.. Diet and habitat definitions for Mexican glyptodonts from Cedral (San Luis Potosí, México) based on stable isotope analysis. Geological Magazine. 149. 1. 2011-10-18. 153–157. 0016-7568. 10.1017/S0016756811000951. 129862616.
  10. Flávio Góis . Laureano Raúl González Ruiz . Gustavo Juan Scillato-Yané . Esteban Soibelzon . 2015 . A Peculiar New Pampatheriidae (Mammalia: Xenarthra: Cingulata) from the Pleistocene of Argentina and Comments on Pampatheriidae Diversity . PLOS ONE . 10 . 6 . e0128296 . 10.1371/journal.pone.0128296 . 26083486 . 4470999. 2015PLoSO..1028296G . free .
  11. Guillaume Billet . Lionel Hautier . Christian de Muizon . Xavier Valentin . 2011 . Oldest cingulate skulls provide congruence between morphological and molecular scenarios of armadillo evolution . Proceedings of the Royal Society . 278 . 1719. 2791–2797. 10.1098/rspb.2010.2443 . 21288952 . 3145180.