TY - JOUR
T1 - Macaque masseter muscle
T2 - Internal architecture, fiber length and cross-sectional area
AU - Antón, S. C.
N1 - Funding Information:
I am indebted to Drs. Bill Hylander, Steve Leigh, Matt Ravosa, Gen Suwa, Tim White, F. Clark Howell, Sharon Swartz, and Bob Full and to the reviewers for their help. The following individuals and institutions provided cadaveral material for this study: Dr D. Weaver, Bowman Gray Medical Center, Wake Forest University; Yerkes Primate Research Institute; Oregon Primate Research Institute; Three Rivers Primate Research Institute, Tulane University; Kyoto Primate Research Institute. S. Schell and T. C. Crawford provided technical assistance. Funding provided by the L. S. B. Leakey and Wenner-Gren Foundations (grant #5481 with F.C.Howell).
PY - 1999
Y1 - 1999
N2 - Models of mastication require knowledge of fiber lengths and physiological cross-sectional area (PCS): a proxy for muscle force. Yet only a small number of macaques of various species, ages, and sexes inform the previous standards for masseter muscle architecture. I dissected 36 masseters from 30 adult females of 3 macaque species - Macaca fascicularis, M. mulatta, M. nemestrina - using gross and chemical techniques and calculated PCS. These macaques have mechanically similar dietary niches and exhibit no significant difference in masseter architecture or fiber length. Intramuscular tendons effectively compartmentalize macaque masseters from medial to lateral. Fiber lengths vary by muscle subsection but are relatively conservative among species. Fiber length does not scale with body size (mass) or masseter muscle mass. However, PCS scales isometrically with body size; larger animals have greater force production capabilities. PCS scales positively allometrically with facial size; animals with more prognathic faces and taller mandibular corpora have greater PCS, and hence force, values. This positive allometry counters the less efficient positioning of masseter muscles in longer-faced animals. In each case, differences in PCS among species result from differences in muscle mass not fiber length. Masseter PCS is only weakly correlated with bone proxies previously used to estimate muscle force. Thus predictions of muscle force from bone parameters will entail large margins of errors and should be used with caution.
AB - Models of mastication require knowledge of fiber lengths and physiological cross-sectional area (PCS): a proxy for muscle force. Yet only a small number of macaques of various species, ages, and sexes inform the previous standards for masseter muscle architecture. I dissected 36 masseters from 30 adult females of 3 macaque species - Macaca fascicularis, M. mulatta, M. nemestrina - using gross and chemical techniques and calculated PCS. These macaques have mechanically similar dietary niches and exhibit no significant difference in masseter architecture or fiber length. Intramuscular tendons effectively compartmentalize macaque masseters from medial to lateral. Fiber lengths vary by muscle subsection but are relatively conservative among species. Fiber length does not scale with body size (mass) or masseter muscle mass. However, PCS scales isometrically with body size; larger animals have greater force production capabilities. PCS scales positively allometrically with facial size; animals with more prognathic faces and taller mandibular corpora have greater PCS, and hence force, values. This positive allometry counters the less efficient positioning of masseter muscles in longer-faced animals. In each case, differences in PCS among species result from differences in muscle mass not fiber length. Masseter PCS is only weakly correlated with bone proxies previously used to estimate muscle force. Thus predictions of muscle force from bone parameters will entail large margins of errors and should be used with caution.
KW - Allometry
KW - Macaca
KW - Mandible
KW - Mastication
KW - Muscle architecture
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U2 - 10.1023/A:1020509006259
DO - 10.1023/A:1020509006259
M3 - Article
AN - SCOPUS:0032789671
SN - 0164-0291
VL - 20
SP - 441
EP - 462
JO - International Journal of Primatology
JF - International Journal of Primatology
IS - 3
ER -