FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2179777798> ?p ?o ?g. }

• W2179777798 endingPage "383" @default.
• W2179777798 startingPage "366" @default.
• W2179777798 abstract "The bony labyrinth provides a proxy for the morphology of the inner ear, a primary cognitive organ involved in hearing, body perception in space, and balance in vertebrates. Bony labyrinth shape variations often are attributed to phylogenetic and ecological factors. Here we use three-dimensional (3D) geometric morphometrics to examine the phylogenetic and ecological patterns of variation in the bony labyrinth morphology of the most species-rich and ecologically diversified traditionally recognized superfamily of Carnivora, the Musteloidea (e.g. weasels, otters, badgers, red panda, skunks, raccoons, coatis). We scanned the basicrania of specimens belonging to 31 species using high-resolution X-ray computed micro-tomography (μCT) to virtually reconstruct 3D models of the bony labyrinths. Labyrinth morphology is captured by a set of six fixed landmarks on the vestibular and cochlear systems, and 120 sliding semilandmarks, slid at the center of the semicircular canals and the cochlea. We found that the morphology of this sensory structure is not significantly influenced by bony labyrinth size, in comparisons across all musteloids or in any of the individual traditionally recognized families (Mephitidae, Procyonidae, Mustelidae). PCA (principal components analysis) of shape data revealed that bony labyrinth morphology is clearly distinguishable between musteloid families, and permutation tests of the Kmult statistic confirmed that the bony labyrinth shows a phylogenetic signal in musteloids and in most mustelids. Both the vestibular and cochlear regions display morphological differences among the musteloids sampled, associated with the size and curvature of the semicircular canals, angles between canals, presence or absence of a secondary common crus, degree of lateral compression of the vestibule, orientation of the cochlea relative to the semicircular canals, proportions of the cochlea, and degree of curvature of its turns. We detected a significant ecological signal in the bony labyrinth shape of musteloids, differentiating semi-aquatic taxa from non-aquatic ones (the taxa assigned to terrestrial, arboreal, semi-arboreal, and semi-fossorial categories), and a significant signal for mustelids, differentiating the bony labyrinths of terrestrial, semi-arboreal, arboreal, semi-fossorial and semi-aquatic species from each other. Otters and minks are distinguished from non-aquatic musteloids by an oval rather than circular anterior canal, sinuous rather than straight lateral canal, and acute rather than straight angle between the posterior and lateral semicircular canals - each of these morphological characters has been related previously to animal sensitivity for detecting head motion in space." @default.
• W2179777798 created "2016-06-24" @default.
• W2179777798 creator A5000196761 @default.
• W2179777798 creator A5047739829 @default.
• W2179777798 creator A5058744638 @default.
• W2179777798 creator A5060181828 @default.
• W2179777798 creator A5082389997 @default.
• W2179777798 date "2015-11-18" @default.
• W2179777798 modified "2023-10-12" @default.
• W2179777798 title "Bony labyrinth shape variation in extant Carnivora: a case study of Musteloidea" @default.
• W2179777798 cites W147128559 @default.
• W2179777798 cites W1527466317 @default.
• W2179777798 cites W1969810115 @default.
• W2179777798 cites W1978779308 @default.
• W2179777798 cites W1983899854 @default.
• W2179777798 cites W1987447288 @default.
• W2179777798 cites W1990221500 @default.
• W2179777798 cites W1991794144 @default.
• W2179777798 cites W1996237160 @default.
• W2179777798 cites W1998731080 @default.
• W2179777798 cites W2001483165 @default.
• W2179777798 cites W2005607962 @default.
• W2179777798 cites W2008611625 @default.
• W2179777798 cites W2008708501 @default.
• W2179777798 cites W2024906165 @default.
• W2179777798 cites W2026108752 @default.
• W2179777798 cites W2028206058 @default.
• W2179777798 cites W2035080425 @default.
• W2179777798 cites W2037357509 @default.
• W2179777798 cites W2039999274 @default.
• W2179777798 cites W2041894030 @default.
• W2179777798 cites W2052119774 @default.
• W2179777798 cites W2056365022 @default.
• W2179777798 cites W2060061695 @default.
• W2179777798 cites W2061276240 @default.
• W2179777798 cites W2062494117 @default.
• W2179777798 cites W2071149137 @default.
• W2179777798 cites W2071976720 @default.
• W2179777798 cites W2073182160 @default.
• W2179777798 cites W2073679218 @default.
• W2179777798 cites W2074209116 @default.
• W2179777798 cites W2083793027 @default.
• W2179777798 cites W2093828180 @default.
• W2179777798 cites W2096494868 @default.
• W2179777798 cites W2101412045 @default.
• W2179777798 cites W2104579758 @default.
• W2179777798 cites W2105532546 @default.
• W2179777798 cites W2112439920 @default.
• W2179777798 cites W2114136084 @default.
• W2179777798 cites W2117105160 @default.
• W2179777798 cites W2117182663 @default.
• W2179777798 cites W2117221169 @default.
• W2179777798 cites W2119646706 @default.
• W2179777798 cites W2124871119 @default.
• W2179777798 cites W2126333522 @default.
• W2179777798 cites W2128409098 @default.
• W2179777798 cites W2128971747 @default.
• W2179777798 cites W2130887463 @default.
• W2179777798 cites W2132786421 @default.
• W2179777798 cites W2133820783 @default.
• W2179777798 cites W2136665575 @default.
• W2179777798 cites W2140775386 @default.
• W2179777798 cites W2147278262 @default.
• W2179777798 cites W2147924430 @default.
• W2179777798 cites W2151409320 @default.
• W2179777798 cites W2152912302 @default.
• W2179777798 cites W2159296820 @default.
• W2179777798 cites W2172186016 @default.
• W2179777798 cites W2207526553 @default.
• W2179777798 cites W2398328369 @default.
• W2179777798 cites W2502086336 @default.
• W2179777798 cites W315886281 @default.
• W2179777798 cites W4297623400 @default.
• W2179777798 cites W790640073 @default.
• W2179777798 doi "https://doi.org/10.1111/joa.12421" @default.
• W2179777798 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5341543" @default.
• W2179777798 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26577069" @default.
• W2179777798 hasPublicationYear "2015" @default.
• W2179777798 type Work @default.
• W2179777798 sameAs 2179777798 @default.
• W2179777798 citedByCount "64" @default.
• W2179777798 countsByYear W21797777982016 @default.
• W2179777798 countsByYear W21797777982017 @default.
• W2179777798 countsByYear W21797777982018 @default.
• W2179777798 countsByYear W21797777982019 @default.
• W2179777798 countsByYear W21797777982020 @default.
• W2179777798 countsByYear W21797777982021 @default.
• W2179777798 countsByYear W21797777982022 @default.
• W2179777798 countsByYear W21797777982023 @default.
• W2179777798 crossrefType "journal-article" @default.
• W2179777798 hasAuthorship W2179777798A5000196761 @default.
• W2179777798 hasAuthorship W2179777798A5047739829 @default.
• W2179777798 hasAuthorship W2179777798A5058744638 @default.
• W2179777798 hasAuthorship W2179777798A5060181828 @default.
• W2179777798 hasAuthorship W2179777798A5082389997 @default.
• W2179777798 hasBestOaLocation W21797777981 @default.
• W2179777798 hasConcept C105702510 @default.
• W2179777798 hasConcept C134018914 @default.

• next