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As herbivorous, diphyodont mammals with relatively low-crowned molars, primates experience changes in dental function during their lifetimes as teeth become progressively worn. Maintaining tooth function with wear is thought to pose a particular challenge for folivorous primates whose diets emphasize molar shearing actions. Recent studies using dental topographic methods suggest that certain primate folivores have molar morphology that maintains or increases functional shearing surfaces with tooth wear (‘dental sculpting’). Evidence for this phenomenon has been found in folivorous but not frugivorous New World monkeys, supporting the hypothesis that dental sculpting is an adaptive trait linked to diet. This analysis extends these methods to two sympatric Old World monkeys from Sabah, Malaysia, possessing distinct diets and dental morphologies: the folivorous colobine Trachypithecus cristatus (n=25) and the more frugivorous cercopithecine Macaca fascicularis (n=22). For each species, 3D shear crest lengths and four dental topographic variables (relief index, slope, angularity, and Dirichlet Normal Energy [DNE]) were measured from variably worn lower second molars. Preliminary results indicate that for any given degree of wear, Trachypithecus has longer shear crest lengths and higher relief, slope, angularity, and DNE than Macaca. The two species exhibit different patterns and degrees of change in topography and shearing crest lengths across the wear series. However, these changes do not always match expectations based on their respective diets. Correlations between 3D shear crest lengths and other dental topographic measurements suggests that the type of metric used to assess shearing potential may affect whether or not dental sculpting is detected.
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The hierarchical radiation of phyllostomid bats as revealed by adaptive molar morphology
Adaptive radiations are bursts in biodiversity that generate new evolutionary lineages and phenotypes. However, because they typically occur over millions of years, it is unclear how their macroevolutionary dynamics vary through time and among groups of organisms. Phyllostomid bats radiated extensively for diverse diets-from insects to vertebrates, fruit, nectar, and blood-and we use their molars as a model system to examine the dynamics of adaptive radiations. Three-dimensional shape analyses of lower molars of Noctilionoidea (Phyllostomidae and close relatives) indicate that different diet groups exhibit distinct morphotypes. Comparative analyses further reveal that phyllostomids are a striking example of a hierarchical radiation; phyllostomids' initial, higher-level diversification involved an "early burst" in molar morphological disparity as lineages invaded new diet-affiliated adaptive zones, followed by subsequent lower-level diversifications within adaptive zones involving less dramatic morphological changes. We posit that strong selective pressures related to initial shifts to derived diets may have freed molars from morpho-functional constraints associated with the ancestral molar morphotype. Then, lineages with derived diets (frugivores and nectarivores) diversified within broad adaptive zones, likely reflecting finer-scale niche partitioning. Importantly, the observed early burst pattern is only evident when examining molar traits that are strongly linked to diet, highlighting the value of ecomorphological traits in comparative studies. Our results support the hypothesis that adaptive radiations are commonly hierarchical and involve different tempos and modes at different phylogenetic levels, with early bursts being more common at higher levels.
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- PAR ID:
- 10507698
- Publisher / Repository:
- Current Biology
- Date Published:
- Journal Name:
- Current Biology
- Volume:
- 34
- Issue:
- 6
- ISSN:
- 0960-9822
- Page Range / eLocation ID:
- 1284 to 1294.e3
- Subject(s) / Keyword(s):
- Noctilionoidea adaptive landscape adaptive radiation comparative methods early burst evolutionary models functional morphology macroevolution molars morphological disparity
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1016/j.cub.2024.02.027
