Literature DB >> 14984783

Does space in the jaw influence the timing of molar crown initiation? A model using baboons (Papio anubis) and great apes (Pan troglodytes, Pan paniscus).

Julia C Boughner1, M Christopher Dean.   

Abstract

Radiographic and histological studies of baboon (Papio hamadryas, P. anubis) and chimpanzee (Pan troglodytes) permanent tooth development have found that periods of molar crown mineralization overlap markedly in chimpanzees but are staggered in baboons. Here we test the hypothesis that these intertaxon differences in molar initiation are primarily due to the space available in the mandibles of each species for these teeth. This study includes radiographic, linear measurement, and three-dimensional (3D) coordinate landmark data taken from baboon (Papio anubis n=51) and great ape (Pan paniscus n=43, P. troglodytes n=60) mandibles and permanent molars across a broad developmental range for each taxon. Unexpectedly, 3D multivariate statistical shape analysis of the molar crypt, crown, and root data shows that all three species trajectories of molar row shape change are indistinguishable from each other. Qualitative analysis of these 3D data reveals subtle and inconclusive intergeneric differences in the space maintained between adjacent molars during growth. The space distal to each newly initiated molar is slightly greater in the baboon. Bivariate analyses comparing molar row and mandibular corpus proportions in Papio and Pan fail to show clear or consistent taxonomic differences in the ratio of space afforded developing molars in the alveolar bone. Thus, there is a poor correlation between mandibular proportion and both intermolar spacing and 3D molar development pattern. Contrary to earlier studies, these results suggest that pattern of molar crown initiation and temporal overlap of adjacent mineralizing crowns is not significantly different between Papio and Pan. This may be due in part to the inclusion here of not only 3D molar crown data but also 3D molar crypt data. This study strongly refutes the hypothesis that space available in the mandible directly underlies different times of permanent molar crown initiation between Papio and Pan.

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Year:  2004        PMID: 14984783     DOI: 10.1016/j.jhevol.2003.11.007

Source DB:  PubMed          Journal:  J Hum Evol        ISSN: 0047-2484            Impact factor:   3.895


  7 in total

1.  Balancing the spatial demands of the developing dentition with the mechanical demands of the catarrhine mandibular symphysis.

Authors:  Samuel N Cobb; Olga Panagiotopoulou
Journal:  J Anat       Date:  2011-01       Impact factor: 2.610

2.  Relative tooth size at birth in primates: Life history correlates.

Authors:  Timothy D Smith; Magdalena N Muchlinski; Wade R Bucher; Christopher J Vinyard; Christopher J Bonar; Sian Evans; Lawrence E Williams; Valerie B DeLeon
Journal:  Am J Phys Anthropol       Date:  2017-08-19       Impact factor: 2.868

3.  Facial ontogeny in Neanderthals and modern humans.

Authors:  Markus Bastir; Paul O'Higgins; Antonio Rosas
Journal:  Proc Biol Sci       Date:  2007-05-07       Impact factor: 5.349

4.  Developmental connections between cranial components and the emergence of the first permanent molar in humans.

Authors:  Marina L Sardi; Fernando Ramírez Rozzi
Journal:  J Anat       Date:  2007-04       Impact factor: 2.610

5.  A biomechanical perspective on molar emergence and primate life history.

Authors:  Halszka Glowacka; Gary T Schwartz
Journal:  Sci Adv       Date:  2021-10-06       Impact factor: 14.136

6.  Human life history evolution explains dissociation between the timing of tooth eruption and peak rates of root growth.

Authors:  M Christopher Dean; Tim J Cole
Journal:  PLoS One       Date:  2013-01-14       Impact factor: 3.240

7.  Making Space for Permanent Molars in Growing Baboon (Papio anubis) and Great Ape (Pan paniscus and P. troglodytes) Mandibles: Possible Ontogenetic Strategies and Solutions.

Authors:  Julia C Boughner
Journal:  Anat Res Int       Date:  2011-06-07
  7 in total

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