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Enamel is the hardest tissue in the vertebrate body. Although variation in enamel microstructure is often linked with diet, the gross proportions of the tissues that compose vertebrate teeth remain relatively unexplored in reptiles. To investigate the patterns of enamel thickness in crocodyliforms, we used micro‐computed tomography scanning to evaluate enamel thickness in teeth of Alligator mississippiensis from rostral, intermediate and caudal locations in the tooth row from an ontogenetic range of animals. We also evaluated enamel thickness in the derived teeth of several extinct crocodyliforms with disparate craniodental morphologies. Our data show that enamel thickness scales isometrically with skull length. We also show that enamel is relatively thicker in caudal teeth than teeth in more rostral positions, concordant with the higher bite forces they experience during feeding. We compared our data with existing enamel thickness data reported from dinosaurs and mammalian taxa to find that archosaurs have markedly thinner enamel than most mammals. These findings serve as a basis for future investigations into the diversity and function of the proportions of dental tissues.
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Bat Dentitions: A Model System for Studies at the Interface of Development, Biomechanics, and Evolution
Abstract The evolution of complex dentitions in mammals was a major innovation that facilitated the expansion into new dietary niches, which imposed selection for tight form–function relationships. Teeth allow mammals to ingest and process food items by applying forces produced by a third-class lever system composed by the jaw adductors, the cranium, and the mandible. Physical laws determine changes in jaw adductor (biting) forces at different bite point locations along the mandible (outlever), thus, individual teeth are expected to experience different mechanical regimes during feeding. If the mammal dentition exhibits functional adaptations to mandible feeding biomechanics, then teeth are expected to have evolved to develop mechanically advantageous sizes, shapes, and positions. Here, we present bats as a model system to test this hypothesis and, more generally, for integrative studies of mammal dental diversity. We combine a field-collected dataset of bite forces along the tooth row with data on dental and mandible morphology across 30 bat species. We (1) describe, for the first time, bite force trends along the tooth row of bats; (2) use phylogenetic comparative methods to investigate relationships among bite force patterns, tooth, and mandible morphology; and (3) hypothesize how these biting mechanics patterns may relate to the developmental processes controlling tooth formation. We find that bite force variation along the tooth row is consistent with predictions from lever mechanics models, with most species having the greatest bite force at the first lower molar. The cross-sectional shape of the mandible body is strongly associated with the position of maximum bite force along the tooth row, likely reflecting mandibular adaptations to varying stress patterns among species. Further, dental dietary adaptations seem to be related to bite force variation along molariform teeth, with insectivorous species exhibiting greater bite force more anteriorly, narrower teeth and mandibles, and frugivores/omnivores showing greater bite force more posteriorly, wider teeth and mandibles. As these craniodental traits are linked through development, dietary specialization appears to have shaped intrinsic mechanisms controlling traits relevant to feeding performance.
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- PAR ID:
- 10349015
- Date Published:
- Journal Name:
- Integrative and Comparative Biology
- ISSN:
- 1540-7063
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Journal Article:
- https://doi.org/10.1093/icb/icac042
