2016
DOI: 10.1002/ajpa.23112
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Hip joint mobility in free‐ranging rhesus macaques

Abstract: Objectives We aimed to test for differences in hip joint range of motion (ROM) between captive and free-ranging rhesus macaques (Macaca mulatta), particularly for hip joint abduction, which previous studies of captive macaques have found to be lower than predicted. Materials and Methods Hip ROM was assessed following standard joint measurement methodology in anesthetized adult free-ranging rhesus macaques (n=39) from Cayo Santiago, and compared to published ROM data from captive rhesus macaques (n=16) (Hammo… Show more

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Cited by 5 publications
(7 citation statements)
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References 31 publications
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“…First, most tetrapods likely generate larger jaw-and/ or limb-joint excursions during discrete, non-cyclic behaviors than during cyclic behaviors (Essner, 2002;Herring and Herring, 1974;Hylander, 2013;Malfait et al, 2014;Rundquist et al, 2009;Vinyard et al, 2011;Williams et al, 2009). That said, we restricted our analysis to data from cyclic (repeated) behaviors because they are important behaviors in all tetrapods, they are available at larger sample sizes across a wider taxonomic breadth than discrete behaviors, and, unlike maximum jaw-joint excursions (Hylander, 2013), reliable estimates of maximum limb joint excursions are difficult to replicate (DeRousseau et al, 1983;Hammond, 2014;Hammond et al, 2017). Discrete and cyclic behaviors are also fundamentally different in their dynamic properties and, therefore, in their motor control, suggesting that combining their joint excursion data in one analysis would be inappropriate (Hogan and Sternad, 2007;Schaal et al, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…First, most tetrapods likely generate larger jaw-and/ or limb-joint excursions during discrete, non-cyclic behaviors than during cyclic behaviors (Essner, 2002;Herring and Herring, 1974;Hylander, 2013;Malfait et al, 2014;Rundquist et al, 2009;Vinyard et al, 2011;Williams et al, 2009). That said, we restricted our analysis to data from cyclic (repeated) behaviors because they are important behaviors in all tetrapods, they are available at larger sample sizes across a wider taxonomic breadth than discrete behaviors, and, unlike maximum jaw-joint excursions (Hylander, 2013), reliable estimates of maximum limb joint excursions are difficult to replicate (DeRousseau et al, 1983;Hammond, 2014;Hammond et al, 2017). Discrete and cyclic behaviors are also fundamentally different in their dynamic properties and, therefore, in their motor control, suggesting that combining their joint excursion data in one analysis would be inappropriate (Hogan and Sternad, 2007;Schaal et al, 2004).…”
Section: Discussionmentioning
confidence: 99%
“…In a naturalistic arboreal setting, it is rare that animals are presented with long tracts of straight, unobstructed supports (Bertram, ; Parsons & Taylor, ). With this in mind, we propose caution in interpreting biomechanical performance variables in the lab, and conclusions should be paired with observations from wild animals in naturalistic settings (Hammond, Johnson, & Higham, ).…”
Section: Discussionmentioning
confidence: 99%
“…These are but a few of the studies of primate functional locomotor morphology appearing in AJPA in the years following the 1967 Evolution of Primate Locomotor Systems issue, and there have been too many to attempt summarizing them all. Like the studies by Grand () and Tuttle (), many offered detailed analyses of specific regions or joint complexes: the shoulder and forelimb (Anapol & Gray, ; Chan, ; Green, ; Green, Sugiura, Seitelman, & Gunz, ; Holliday & Friedl, ; Kimes, Siegel, & Sadler, ; Larson, ; Püschel & Sellers, ; Selby & Lovejoy, ; Shea, ; Squyres & DeLeon, ; Swartz, ; Turnquist ), the wrist and hand (Cartmill, ; Hamrick, ; Lemelin & Schmitt, ; Lewis, ; Marzke, ; O'Connor, ; Susman, ; Young & Heard‐Booth, ), the pelvis, hip and hind limb (Anapol & Barry, ; Anapol & Jungers, ; Anemone, ; Gebo, ; Hammond, ; Hammond, Plavcan, & Ward, ; Hammond, Johnson, & Higham, ; Hamrick, ; Lewton, ; McHenry & Corruccini, ; Oxnard, German, Jouffroy, & Lessertisseur, ; Oxnard, German, & McArdle, ), the ankle and foot (DeSilva, ; Gebo, ; Goodenberger et al, ; Lewis, ; Lisowski, Albrecht, & Oxnard, ; Meldrum, Dagosto, & White, ; Nowak, Carlson, & Patel, ), and the trunk and vertebral column (Curtis, ; German, ; Johnson & Shapiro, ; Russo, ; Shapiro, ).…”
Section: Functional Analysis Of Primate Locomotor Morphologymentioning
confidence: 99%