Literature DB >> 19402068

Functional correlates of fiber architecture of the lateral caudal musculature in prehensile and nonprehensile tails of the platyrrhini (primates) and procyonidae (carnivora).

Jason M Organ1, Mark F Teaford, Andrea B Taylor.   

Abstract

Prehensile-tailed platyrrhines (atelines and Cebus) and procyonids (Potos) display bony tail features that have been functionally and adaptively linked to their prehensile behaviors, particularly the need to resist relatively greater bending and torsional stresses associated with supporting their body weight during suspensory postures. We compared fiber architecture of the mm. intertransversarii caudae (ITC), the prime tail lateral flexors/rotators, in 40 individuals distributed across 8 platyrrhine and 2 procyonid genera, divided into one of two groups: prehensile or nonprehensile. We tested the hypothesis that prehensile-tailed taxa exhibit relatively greater physiologic cross-sectional areas (PCSAs) to maintain tail suspensory postures for extended periods. As an architectural trade-off of maximizing force, we also predicted prehensile-tailed taxa would exhibit relatively shorter, more pinnate fibers, and a lower mass to tetanic tension ratio (Mass/P(O)). Prehensile-tailed taxa have relatively higher PCSAs in all tail regions, indicating their capacity to generate relatively greater maximum muscle forces compared to nonprehensile-tailed taxa. Contrary to our predictions, there are no group differences in pinnation angles, fiber lengths or M/P(O) ratios. Therefore, the relatively greater prehensile PCSAs are driven largely by relative increase in muscle mass. These findings suggest that relatively greater ITC PCSAs can be functionally linked to the need for prehensile-tailed taxa to suspend and support their body weight during arboreal behaviors. Moreover, maximizing ITC force production may not come at the expense of muscle excursion/contraction velocity. One advantage of this architectural configuration is it facilitates suspension of the body while simultaneously maximizing tail contact with the substrate. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19402068     DOI: 10.1002/ar.20886

Source DB:  PubMed          Journal:  Anat Rec (Hoboken)        ISSN: 1932-8486            Impact factor:   2.064


  6 in total

1.  Substrate use drives the macroevolution of mammalian tail length diversity.

Authors:  Sarah T Mincer; Gabrielle A Russo
Journal:  Proc Biol Sci       Date:  2020-02-05       Impact factor: 5.349

2.  Epaxial muscle fiber architecture favors enhanced excursion and power in the leaper Galago senegalensis.

Authors:  Emranul Huq; Christine E Wall; Andrea B Taylor
Journal:  J Anat       Date:  2015-07-16       Impact factor: 2.610

3.  Glucocorticoids Induce Bone and Muscle Atrophy by Tissue-Specific Mechanisms Upstream of E3 Ubiquitin Ligases.

Authors:  Amy Y Sato; Danielle Richardson; Meloney Cregor; Hannah M Davis; Ernie D Au; Kevin McAndrews; Teresa A Zimmers; Jason M Organ; Munro Peacock; Lilian I Plotkin; Teresita Bellido
Journal:  Endocrinology       Date:  2017-03-01       Impact factor: 4.736

4.  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

5.  Interplay between postcranial morphology and locomotor types in Neotropical sigmodontine rodents.

Authors:  Luz V Carrizo; María J Tulli; Daniel A Dos Santos; Virginia Abdala
Journal:  J Anat       Date:  2013-12-26       Impact factor: 2.610

6.  Skeletal determinants of tail length are different between macaque species groups.

Authors:  Hikaru Wakamori; Yuzuru Hamada
Journal:  Sci Rep       Date:  2019-02-04       Impact factor: 4.379

  6 in total

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