Summary 1.Bite force is an important performance measure for vertebrate and is related to a variety of ecological challenges. Phyllostomid bats present highly diversified feeding habits associated with extensive cranial shape divergence. Biomechanical models predict that the cranial shape changes are linked to dietary variation through bite force. However, the relationship of cranial shape, diet and bite force had not been explicitly tested before. 2.Here we use a combination of geometric morphometric techniques and comparative methods to test for morphological correlates of bite force and diet in 14 phyllostomid bat species. Skull and mandible shape variation were assessed by vectors, derived from a two-block partial least squares analysis of geometric shape and size-independent bite forces. The relationship between bite force, skull shape and diet was assessed by phylogenetic generalized least square regressions. 3. Most variation in the bite force data examined here (approximately 74%) was explained by size variation alone, but the shape vectors for both skull and mandible explained a significant part of the residual variation in bite force (83% and 56%, respectively), as did the dietary differences (56%). Although the first principal component of diet variation is associated with a negative correlation between insectivory and frugivory, residual bite force and cranial shape are not associated with this diet contrast. Shape and residual bite force variation in the sample were strongly associated with the second diet component, depicting an increase in nectarivory. 4. Species with stronger bites (insectivorous and frugivorous) than expected for their sizes presented a shorter rostrum and mandible, higher skulls, and more developed muscle attachment areas. On the other hand, the characteristic cranial elongation of nectarivorous species (supporting the long tongue) is a trade-off with bite force. These morphological correlates of bite force are similar to those observed in carnivores and non-herbivorous marsupials, and can be related to morphological characters used in biomechanical models for bite force prediction. 5. Our results reinforce the effectiveness of statistically integrating geometric shape variables to bite force and diet information in the investigation of patterns of cranial shape change and trophic radiation in ecologically diverse vertebrate groups.
The rodent mandible has become a paradigm for studies on the development and evolution of complex morphological structures. We use a combination of geometric and multivariate morphometric methods in order to assess the correspondence between integration patterns and a priori biological models in the context of evolutionary shape divergence in the mandible of rodents of the family Echimyidae. The correlation of shape distances among operational taxonomic units (individuals, species, genera) in separate morphogenetic components allowed the construction of integration matrices among mandible components for data sets corresponding to varying levels of genetic divergence (intergeneric, interspecific, and intrapopulational). The integration matrices were associated with a priori biological (developmental, genetical, modular) models, and the maximum integration axes (singular warps) were compared with realized axes of maximum interspecific variation (relative warps). The integration pattern and intensity were not stable in data sets with different levels of genetic divergence, and the varying functional demands during the ecological radiation in the family were probably responsible for the differences in observed integration patterns. Developmental and genetic models were significantly associated with the interspecific integration patterns observed, suggesting a role for neutral evolution during the evolutionary divergence of mandible shape. However, directional and stabilizing selection were not discarded as processes responsible for the generation of interspecific integration. The choreography of the morphogenetic components in the mandible is highly flexible and the integrated groups of components can be reorganized depending on functional demands during evolutionary shape changes.
The evolutionary integration of complex morphological structures is a macroevolutionary pattern in which morphogenetic components evolve in a coordinated fashion, which can result from the interplay among processes of developmental, genetic integration, and different types of selection. We tested hypotheses of ecological versus developmental factors underlying patterns of within-species and evolutionary integration in the mandible of phyllostomid bats, during the most impressive ecological and morphological radiation among mammals. Shape variation of mandibular morphogenetic components was associated with diet, and the transition of integration patterns from developmental to within-species to evolutionary was examined. Within-species (as a proxy to genetic) integration in different lineages resembled developmental integration regardless of diet specialization, however, evolutionary integration patterns reflected selection in different mandibular components. For dietary specializations requiring extensive functional changes in mastication patterns or biting, such as frugivores and sanguivores, the evolutionary integration pattern was not associated with expected within-species or developmental integration. On the other hand, specializations with lower mastication demands or without major functional reorganization (such as nectarivores and carnivores), presented evolutionary integration patterns similar to the expected developmental pattern. These results show that evolutionary integration patterns are largely a result of independent selection on specific components regardless of developmental modules.
BackgroundThe phyllostomid bats present the most extensive ecological and phenotypic radiation known among mammal families. This group is an important model system for studies of cranial ecomorphology and functional optimisation because of the constraints imposed by the requirements of flight. A number of studies supporting phyllostomid adaptation have focused on qualitative descriptions or correlating functional variables and diet, but explicit tests of possible evolutionary mechanisms and scenarios for phenotypic diversification have not been performed. We used a combination of morphometric and comparative methods to test hypotheses regarding the evolutionary processes behind the diversification of phenotype (mandible shape and size) and diet during the phyllostomid radiation.ResultsThe different phyllostomid lineages radiate in mandible shape space, with each feeding specialisation evolving towards different axes. Size and shape evolve quite independently, as the main directions of shape variation are associated with mandible elongation (nectarivores) or the relative size of tooth rows and mandibular processes (sanguivores and frugivores), which are not associated with size changes in the mandible. The early period of phyllostomid diversification is marked by a burst of shape, size, and diet disparity (before 20 Mya), larger than expected by neutral evolution models, settling later to a period of relative phenotypic and ecological stasis. The best fitting evolutionary model for both mandible shape and size divergence was an Ornstein-Uhlenbeck process with five adaptive peaks (insectivory, carnivory, sanguivory, nectarivory and frugivory).ConclusionsThe radiation of phyllostomid bats presented adaptive and non-adaptive components nested together through the time frame of the family's evolution. The first 10 My of the radiation were marked by strong phenotypic and ecological divergence among ancestors of modern lineages, whereas the remaining 20 My were marked by stasis around a number of probable adaptive peaks. A considerable amount of cladogenesis and speciation in this period is likely to be the result of non-adaptive allopatric divergence or adaptations to peaks within major dietary categories.
Evolutionary radiations on continents are less well-understood and appreciated than those occurring on islands. The extent of ecological influence on species divergence can be evaluated to determine whether a radiation was ultimately the outcome of divergent natural selection or else arose mainly by nonecological divergence. Here, we used phylogenetic comparative methods to test distinct hypotheses corresponding to adaptive and nonadaptive evolutionary scenarios for the morphological evolution of sigmodontine rodents. Results showed that ecological variables (diet and life-mode) explain little of the shape and size variation of sigmodontine skulls and mandibles. A Brownian model with varying rates for insectivory versus all other diets was the most likely evolutionary model. The insectivorous sigmodontines have a faster rate of morphological evolution than mice feeding on other diets, possibly due to stronger selection for features that aid insectivory. We also demonstrate that rapid early-lineage diversification is not accompanied by high morphological divergence among subclades, contrasting with island results. The geographic size of continents permits spatial segregation to a greater extent than on islands, allowing for allopatric distributions and escape from interspecific competition. We suggest that continental radiations of rodents are likely to produce a pattern of high species diversification coupled with a low degree of phenotypic specialization.
The causes of craniofacial variation among human populations have been the subject of controversy. In this work, we studied aboriginal populations from southern South America, the last continental region peopled by humans and with a wide range of ecological conditions. Because of these characteristics, southern South America provides a unique opportunity to study the relative importance of random and nonrandom factors in human diversification. Previous craniometric studies recognized remarkable differences among populations from this region, usually resorting to random factors as the main explanation. In contrast, here we suggest, using tests based on quantitative genetic models, that: (1) the rate of craniofacial divergence among these populations is too high and (2) the patterns of variation within and between populations are too different to be explained by genetic drift alone. In addition, the among-sample craniofacial variation is correlated with climate and diet but not with mtDNA variation. We suggest that the influence of nonrandom factors (e.g., plasticity, selection) on human craniofacial diversification in regions with large ecological variation is more important than generally acknowledged and capable to generate large craniofacial divergence in a short period of time. These results bring nonrandom factors into focus for the interpretation of human craniofacial variation. K E Y W O R D S :Ecological variation, evolutionary rates, geometric morphometrics, Patagonian populations.
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