Literature DB >> 21456028

Microstructure of dental hard tissues in fossil and recent xenarthrans (Mammalia: Folivora and Cingulata).

Daniela C Kalthoff1.   

Abstract

A striking difference between xenarthrans and other mammals is the complete loss of tooth enamel in all members but the earliest armadillos. However, sloth and armadillo teeth show structured wear facets, which in all other mammals are formed by tooth enamel. How is that possible? Here, I report about an analysis of fossil and recent xenarthran dental hard tissue microstructure. It shows that osteodentine is not exclusive to fossil Cingulata, but also occurs in some recent taxa. Furthermore, I found profound modifications of orthodentine architecture in comparison to other mammals. Remarkable features are (a) a larger proportion of the highly mineralized, collagen-free peritubular dentine, and (b) a modified architecture of the odontoblastic process with frequent interconnections between the extensions and unusually intensive branching of the extensions forming a complex meshwork, penetrating the intertubular dentine matrix. The orthodentine microstructural build-up is unique in Folivora and Cingulata.
Copyright © 2011 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2011        PMID: 21456028     DOI: 10.1002/jmor.10937

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  9 in total

1.  When xenarthrans had enamel: insights on the evolution of their hypsodonty and paleontological support for independent evolution in armadillos.

Authors:  Martín R Ciancio; Emma C Vieytes; Alfredo A Carlini
Journal:  Naturwissenschaften       Date:  2014-07-20

2.  Dietary adaptions in the ultrastructure of dinosaur dentine.

Authors:  Kirstin S Brink; Yu-Cheng Chen; Ya-Na Wu; Wei-Min Liu; Dar-Bin Shieh; Timothy D Huang; Chi-Kuang Sun; Robert R Reisz
Journal:  J R Soc Interface       Date:  2016-12       Impact factor: 4.118

3.  Cranial osteology of the pampathere Holmesina floridanus (Xenarthra: Cingulata; Blancan NALMA), including a description of an isolated petrosal bone.

Authors:  Timothy J Gaudin; Lauren M Lyon
Journal:  PeerJ       Date:  2017-12-11       Impact factor: 2.984

4.  Dental malformations associated with biallelic MMP20 mutations.

Authors:  Shih-Kai Wang; Hong Zhang; Michael B Chavez; Yuanyuan Hu; Figen Seymen; Mine Koruyucu; Yelda Kasimoglu; Connor D Colvin; Tamara N Kolli; Michelle H Tan; Yin-Lin Wang; Pei-Ying Lu; Jung-Wook Kim; Brian L Foster; John D Bartlett; James P Simmer; Jan C-C Hu
Journal:  Mol Genet Genomic Med       Date:  2020-06-03       Impact factor: 2.183

5.  Feeding Ecology in Oligocene Mylodontoid Sloths (Mammalia, Xenarthra) as Revealed by Orthodentine Microwear Analysis.

Authors:  Daniela C Kalthoff; Jeremy L Green
Journal:  J Mamm Evol       Date:  2017-07-28       Impact factor: 2.611

6.  A year in the life of a giant ground sloth during the Last Glacial Maximum in Belize.

Authors:  Jean T Larmon; H Gregory McDonald; Stanley Ambrose; Larisa R G DeSantis; Lisa J Lucero
Journal:  Sci Adv       Date:  2019-02-27       Impact factor: 14.136

7.  Early evidence of molariform hypsodonty in a Triassic stem-mammal.

Authors:  Tomaz P Melo; Ana Maria Ribeiro; Agustín G Martinelli; Marina Bento Soares
Journal:  Nat Commun       Date:  2019-06-28       Impact factor: 14.919

8.  A new rhynchocephalian from the late jurassic of Germany with a dentition that is unique amongst tetrapods.

Authors:  Oliver W M Rauhut; Alexander M Heyng; Adriana López-Arbarello; Andreas Hecker
Journal:  PLoS One       Date:  2012-10-31       Impact factor: 3.240

9.  Phylogenetic signal in tooth wear dietary niche proxies.

Authors:  Danielle Fraser; Ryan J Haupt; W Andrew Barr
Journal:  Ecol Evol       Date:  2018-05-03       Impact factor: 2.912

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.