2021
DOI: 10.1002/ajp.23246
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Quantification of enamel decussation in gracile and robust capuchins (Cebus, Sapajus, Cebidae, Platyrrhini)

Abstract: Multiple behavioral and biomechanical analyses have demonstrated that capuchin monkeys (Cebus and Sapajus) are specialized for breaking down hard-object foods as compared to other cebid monkeys. In addition to a complex suite of craniodental adaptations, it has specifically been demonstrated that capuchins possess highly complex dental enamel, with extensive Hunter-Schreger banding and other decussation, that likely serve as an adaptation to resist crack propagation during hard-object feeding. Furthermore, it … Show more

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Cited by 4 publications
(6 citation statements)
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“…Quantitative evaluation of optical micrographs taken with circularly polarized light has proven to be useful for HSB analysis (Hogg & Richardson, 2019). This technique revealed differences of enamel complexity in case of different monkey species, which was attributed to different masticatory loads (Hogg & Elokda, 2021). Mouse enamel was investigated using SEM micrographs by measuring precisely the angle and number of prisms and the complexity of their arrangement was discussed (Smith et al, 2019).…”
Section: Highlightsmentioning
confidence: 99%
“…Quantitative evaluation of optical micrographs taken with circularly polarized light has proven to be useful for HSB analysis (Hogg & Richardson, 2019). This technique revealed differences of enamel complexity in case of different monkey species, which was attributed to different masticatory loads (Hogg & Elokda, 2021). Mouse enamel was investigated using SEM micrographs by measuring precisely the angle and number of prisms and the complexity of their arrangement was discussed (Smith et al, 2019).…”
Section: Highlightsmentioning
confidence: 99%
“…and the untufted forms represent Cebus sp. The more robust morphology of Sapajus relative to Cebus is characterized by larger teeth, thicker mandibular corpora and symphyses, prominent and anteriorly positioned feeding muscles, greater temporalis physiological cross‐sectional area, and more sinuous sagittal sutures (Figure 1; Anapol & Lee, 1994; Byron, 2009; Chai, 2020; Daegling, 1992; Kinzey, 1974; Masterson, 1997; Hogg and Elokda, 2021; Silva Jr., 2001, 2002; Spencer, 2003; Taylor & Vinyard, 2009; Teaford et al, 2020; Wright, 2005). These features are probable adaptations for consumption of tougher foods in Sapajus relative to Cebus , and a seed predation strategy including obdurate foods, such as palm nuts (Cole, 1992; Defler, 1979a; Defler, 1979b; Freese et al, 1981; Izawa, 1979; Kinzey, 1974; Teaford, 1985; Teaford et al, 2020; Wright, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…With respect to enamel decussation, i.e., the crisscrossing of prisms in enamel, we assessed “enamel complexity”, defined as “any microanatomical feature of dental enamel that increases the heterogeneity of enamel crystallite orientations” ( Hogg & Elokda, 2021 ). The greater the heterogeneity of enamel prism orientations, the more difficult it is for cracks to propagate along prism boundaries ( Hogg & Elokda, 2021 ; Bajaj & Arola, 2009 ). Decussation appears to be more complex in the enamel of mammalian species that experience high loading forces on their teeth ( Hogg & Elokda, 2021 ).…”
Section: Introductionmentioning
confidence: 99%
“…The greater the heterogeneity of enamel prism orientations, the more difficult it is for cracks to propagate along prism boundaries ( Hogg & Elokda, 2021 ; Bajaj & Arola, 2009 ). Decussation appears to be more complex in the enamel of mammalian species that experience high loading forces on their teeth ( Hogg & Elokda, 2021 ). For example, marked enamel complexity in the canines of robust capuchins has been linked ( Hogg & Elokda, 2021 ) to the high bite forces this species uses to process hard foods ( Wright, 2005 ; Alfaro, Silva Jr & Rylands, 2012 ).…”
Section: Introductionmentioning
confidence: 99%
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