2018
DOI: 10.1007/s10914-017-9424-7
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Skull Ontogeny of the Hyraxes Procavia capensis and Dendrohyrax arboreus (Procaviidae: Hyracoidea)

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Cited by 7 publications
(4 citation statements)
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“…Nine-banded armadillos are no exception with nearly 28% of the total cranial shape variation explained by size at the ontogenetic level. The two major ontogenetic allometric trends detected here were the relative snout elongation and the reduction of braincase proportions, which is reminiscent of previous results dealing with mammalian species (Drake & Klingenberg, 2008;Moyano et al, 2018;Heck et al, 2019). This pattern, often designated as craniofacial allometry, was also detected at the evolutionary level in many groups of mammals (Cardini & Polly, 2013;Cardini et al, 2015;Tamagnini et al, 2017).…”
Section: Entire Skull Approachsupporting
confidence: 84%
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“…Nine-banded armadillos are no exception with nearly 28% of the total cranial shape variation explained by size at the ontogenetic level. The two major ontogenetic allometric trends detected here were the relative snout elongation and the reduction of braincase proportions, which is reminiscent of previous results dealing with mammalian species (Drake & Klingenberg, 2008;Moyano et al, 2018;Heck et al, 2019). This pattern, often designated as craniofacial allometry, was also detected at the evolutionary level in many groups of mammals (Cardini & Polly, 2013;Cardini et al, 2015;Tamagnini et al, 2017).…”
Section: Entire Skull Approachsupporting
confidence: 84%
“…3). The relation with cranial size differs between OBUs, which is in line with bivariate analyses demonstrating that most distances measured on mammalian skulls follow different allometric trends (e.g., Abdala et al, 2001;Marroig & Cheverud, 2004;Goswami & Prochel, 2007;Wilson, 2011;Segura & Prevosti, 2012;Moyano et al, 2018).…”
Section: Heterogeneity Of Cranial Allometry In Space and Timesupporting
confidence: 82%
“…This missing DX in Procavia can also be explained by a reduction of the diastema, a structure often considered as a toothless gap in mammals (e.g., Peterkova et al, 2006;Prochazka et al, 2009). Moyano et al (2019) reported the negative allometry of the diastema during skull growth in Procavia, contrasting with the positive allometry of their cheek tooth row, conversely to Dendrohyrax. This relative reduction of the diastema in Procavia might thus be tightly associated with developmental mechanisms inhibiting the DX.…”
Section: Canine Complexity In Extinct and Living Hyracoids And The DX Locusmentioning
confidence: 99%
“…The morphology of the orbits and related structures (e.g., postorbital bar, position and shape of zygomatic arch) is very variable among clades and may be related to different masticatory models (e.g., less lateralized orbits when the mm. temporales show large development; see Noble et al 2000;Cox 2008;Hautier et al 2012), the development of other structures (e.g., bullae; Howell 1932), habitats exploited, and different daily activity patterns (e.g., Hautier et al 2012;Moyano et al 2018;Olivares et al 2020). Among the studied pachyrukhines, P. typicum possesses orbits with the more marked lateral orientation, enabling a wider angle of vision (enhanced panoramic visual field; Howell 1932;Heesy 2004).…”
Section: Eyes and Visionmentioning
confidence: 99%