2013
DOI: 10.1016/j.jhevol.2012.10.006
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Positional behavior and substrate use of Micromys minutus (Rodentia: Muridae): Insights for understanding primate origins

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Cited by 26 publications
(30 citation statements)
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“…Other comparative studies have shown that some terminal-branch specialists such as arboreal marsupials (Cartmill 1974b;Lemelin 1999;Rasmussen 1990;Rasmussen and Sussman 2007;Schmitt and Lemelin 2002;Shapiro and Young 2010;Youlatos 2008), and chameleons (Cartmill 1974b;Herrel et al 2012) possess a hand and foot morphology that is functionally similar to that of primates, suggesting evolutionary convergence of grasping. Recent studies have also demonstrated that species lacking primate grasping adaptations, including some squirrels (Orkin and Pontzer 2011;Samaras and Youlatos 2010) and mice (Byron et al 2011;Urbani and Youlatos 2013), are also capable of moving, feeding, and foraging on thin and terminal branches.…”
Section: Introductionmentioning
confidence: 99%
“…Other comparative studies have shown that some terminal-branch specialists such as arboreal marsupials (Cartmill 1974b;Lemelin 1999;Rasmussen 1990;Rasmussen and Sussman 2007;Schmitt and Lemelin 2002;Shapiro and Young 2010;Youlatos 2008), and chameleons (Cartmill 1974b;Herrel et al 2012) possess a hand and foot morphology that is functionally similar to that of primates, suggesting evolutionary convergence of grasping. Recent studies have also demonstrated that species lacking primate grasping adaptations, including some squirrels (Orkin and Pontzer 2011;Samaras and Youlatos 2010) and mice (Byron et al 2011;Urbani and Youlatos 2013), are also capable of moving, feeding, and foraging on thin and terminal branches.…”
Section: Introductionmentioning
confidence: 99%
“…Although there remains disagreement in the literature as to primate ancestral body size (Soligo and Martin, , ; Silcox et al., ), a presumed small body size for the primate ancestral condition (i.e., less than 100 g) (e.g., Cartmill, ; Gebo, ) is well supported by the small size of the earliest fossil euprimates (Silcox et al., ; Fleagle, ), and by the fact that agreement between paleontological and molecular estimates of primate divergence times improves when molecular models account for the fast life history patterns associated with a small bodied last common ancestor (Steiper and Seiffert, ). Accordingly, insights on primate locomotor evolution have been gained from studies examining the unique biomechanical benefits and challenges encountered by small primates or other small mammals moving quadrupedally on arboreal substrates (Pridmore, ; Preuschoft et al., ; Arms et al., ; Lemelin et al., ; Lammers and Biknevicius, ; Lammers et al., ; Lemelin and Schmitt, ; Lammers, , ; Lammers and Gauntner, ; Schmidt, ; Youlatos, ; Young, ; Samaras and Youlatos, ; Schmidt and Fischer, , ; Shapiro and Young, , ; Byron et al., ; Lammers and Zurcher, ; Stevens et al., ; Urbani and Youlatos, ; Shapiro et al., ; Chadwell and Young, ; Hesse et al., ; Karantanis et al., ). Most previous studies of primate quadrupedalism have been restricted to the analysis of symmetrical gaits.…”
mentioning
confidence: 99%
“…ancestor (Steiper and Seiffert, 2012). Accordingly, insights on primate locomotor evolution have been gained from studies examining the unique biomechanical benefits and challenges encountered by small primates or other small mammals moving quadrupedally on arboreal substrates (Pridmore, '94;Preuschoft et al, '96;Arms et al, 2002;Lemelin et al, 2003;Lammers and Biknevicius, 2004;Lammers et al, 2006;Lemelin and Schmitt, 2007;Lammers, 2007Lammers, , 2009Lammers and Gauntner, 2008;Schmidt, 2008;Youlatos, 2008;Young, 2009;Samaras and Youlatos, 2010;Fischer, 2010, 2011;Young, 2010, 2012;Byron et al, 2011;Lammers and Zurcher, 2011;Stevens et al, 2011;Urbani and Youlatos, 2013;Shapiro et al, 2014;Chadwell and Young, 2015;Hesse et al, 2015;Karantanis et al, 2015). Most previous studies of primate quadrupedalism have been restricted to the analysis of symmetrical gaits.…”
mentioning
confidence: 99%
“…Moreover, earlier studies of lab mice and the rodent genus Peromyscus have emphasized the role of tail use, increased talar neck angle, and first metatarsal morphology in climbing behaviors (Siegel, ; Siegel and Van Meter, ; Siegel and Jones, ). Recent work with the harvest mouse ( Micromys minutus ; Urbani and Youlatos, ) substantiate this approach that early stages of primate evolution can be modeled with living rodent species. By combining tiny‐size and secure hallucal grasping, those authors demonstrate that animals not typically viewed as being specialized for the fine‐branch niche can nevertheless exploit this habitat to a degree of proficiency that is between the hypothesized Stages 2 and 3 of primate evolution.…”
Section: Introductionmentioning
confidence: 94%