Literature DB >> 15281057

Comparative analysis of masseter fiber architecture in tree-gouging (Callithrix jacchus) and nongouging (Saguinus oedipus) callitrichids.

Andrea B Taylor1, Christopher J Vinyard.   

Abstract

Common marmosets (Callithrix jacchus) and cotton-top tamarins (Saguinus oedipus) (Callitrichidae, Primates) share a broadly similar diet of fruits, insects, and tree exudates. Common marmosets, however, differ from tamarins by actively gouging trees with their anterior teeth to elicit tree exudate flow. During tree gouging, marmosets produce relatively large jaw gapes, but do not necessarily produce relatively large bite forces at the anterior teeth. We compared the fiber architecture of the masseter muscle in tree-gouging Callithrix jacchus (n = 10) to nongouging Saguinus oedipus (n = 8) to determine whether the marmoset masseter facilitates producing these large gapes during tree gouging. We predict that the marmoset masseter has relatively longer fibers and, hence, greater potential muscle excursion (i.e., a greater range of motion through increased muscle stretch). Conversely, because of the expected trade-off between excursion and force production in muscle architecture, we predict that the cotton-top tamarin masseter has more pinnate fibers and increased physiological cross-sectional area (PCSA) as compared to common marmosets. Likewise, the S. oedipus masseter is predicted to have a greater proportion of tendon relative to muscle fiber as compared to the common marmoset masseter. Common marmosets have absolutely and relatively longer masseter fibers than cotton-top tamarins. Given that fiber length is directly proportional to muscle excursion and by extension contraction velocity, this result suggests that marmosets have masseters designed for relatively greater stretching and, hence, larger gapes. Conversely, the cotton-top tamarin masseter has a greater angle of pinnation (but not significantly so), larger PCSA, and higher proportion of tendon. The significantly larger PCSA in the tamarin masseter suggests that their masseter has relatively greater force production capabilities as compared to marmosets. Collectively, these results suggest that the fiber architecture of the common marmoset masseter is part of a suite of features of the masticatory apparatus that facilitates the production of relatively large gapes during tree gouging. Copyright 2004 Wiley-Liss, Inc.

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Year:  2004        PMID: 15281057     DOI: 10.1002/jmor.10249

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


  13 in total

1.  In vivo bone strain and finite element modeling of a rhesus macaque mandible during mastication.

Authors:  Olga Panagiotopoulou; José Iriarte-Diaz; Simon Wilshin; Paul C Dechow; Andrea B Taylor; Hyab Mehari Abraha; Sharifah F Aljunid; Callum F Ross
Journal:  Zoology (Jena)       Date:  2017-09-01       Impact factor: 2.240

2.  Finite element analysis of performance in the skulls of marmosets and tamarins.

Authors:  Elizabeth R Dumont; Julian L Davis; Ian R Grosse; Anne M Burrows
Journal:  J Anat       Date:  2011-01       Impact factor: 2.610

3.  Modeling the biomechanics of articular eminence function in anthropoid primates.

Authors:  Claire E Terhune
Journal:  J Anat       Date:  2011-09-16       Impact factor: 2.610

4.  A preliminary analysis of the relationship between jaw-muscle architecture and jaw-muscle electromyography during chewing across primates.

Authors:  Christopher J Vinyard; Andrea B Taylor
Journal:  Anat Rec (Hoboken)       Date:  2010-04       Impact factor: 2.064

5.  The influence of jaw-muscle fibre-type phenotypes on estimating maximum muscle and bite forces in primates.

Authors:  Megan Holmes; Andrea B Taylor
Journal:  Interface Focus       Date:  2021-08-13       Impact factor: 3.906

6.  The morphology of the masticatory apparatus facilitates muscle force production at wide jaw gapes in tree-gouging common marmosets (Callithrix jacchus).

Authors:  C M Eng; S R Ward; C J Vinyard; A B Taylor
Journal:  J Exp Biol       Date:  2009-12       Impact factor: 3.312

7.  Jaw-muscle fiber architecture in tufted capuchins favors generating relatively large muscle forces without compromising jaw gape.

Authors:  Andrea B Taylor; Christopher J Vinyard
Journal:  J Hum Evol       Date:  2009-10-28       Impact factor: 3.895

8.  Dynamic Musculoskeletal Functional Morphology: Integrating diceCT and XROMM.

Authors:  Courtney P Orsbon; Nicholas J Gidmark; Callum F Ross
Journal:  Anat Rec (Hoboken)       Date:  2018-02       Impact factor: 2.064

9.  Comparative microanatomy of the orbicularis oris muscle between chimpanzees and humans: evolutionary divergence of lip function.

Authors:  Carolyn R Rogers; Mark P Mooney; Timothy D Smith; Seth M Weinberg; Bridget M Waller; Lisa A Parr; Beth A Docherty; Christopher J Bonar; Lauren E Reinholt; Frederic W-B Deleyiannis; Michael I Siegel; Mary L Marazita; Anne M Burrows
Journal:  J Anat       Date:  2009-01       Impact factor: 2.610

10.  Vegetable exudates as food for Callithrix spp. (Callitrichidae): exploratory patterns.

Authors:  Talitha Mayumi Francisco; Dayvid Rodrigues Couto; José Cola Zanuncio; José Eduardo Serrão; Ita de Oliveira Silva; Vanner Boere
Journal:  PLoS One       Date:  2014-11-05       Impact factor: 3.240

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