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Modern Applied Statistics With S

Analyses of morphological disparity have been used to characterize and investigate the evolution of variation in the anatomy, function and ecology of organisms since the 1980s. While a diversity of methods have been employed, it is unclear whether they provide equivalent insights. Here, we review the most commonly used approaches for characterizing and analysing morphological disparity, all of which have associated limitations that, if ignored, can lead to misinterpretation. We propose best practice guidelines for disparity analyses, while noting that there can be no 'one-size-fits-all' approach. The available tools should always be used in the context of a specific biological question that will determine data and method selection at every stage of the analysis.

/pdf/disparities-in-the-analysis-of-morphological-disparity-2885rp0m66.pdf

Disparities in the analysis of morphological disparity

Mosaic evolution refers to the pattern whereby different organismal traits exhibit differential rates of evolution typically due to reduced levels of trait covariation through deep time (i.e., modularity). These differences in rates can be attributed to variation in responses to selective pressures between individual traits. Differential responses to selective pressures also have the potential to facilitate functional specialization, allowing certain traits to track environmental stimuli more closely than others. The teleost skull is a multifunctional structure comprising a complex network of bones and thus an excellent system for which to study mosaic evolution. Here we construct an ultrametric phylogeny for a clade of Neotropical electric fishes (Apteronotidae: Gymnotiformes) and use three-dimensional geometric morphometrics to investigate patterns of mosaic evolution in the skull and jaws. We find strong support for a developmental, three-module hypothesis that consists of the face, braincase, and mandible, and we find that the mandible has evolved four times faster than its neighboring modules. We hypothesize that the functional specialization of the mandible in this group of fishes has allowed it to outpace the face and braincase and evolve in a more decoupled manner. We also hypothesize that this pattern of mosaicism may be widespread across other clades of teleost fishes.

Bony Patchwork: Mosaic Patterns of Evolution in the Skull of Electric Fishes (Apteronotidae: Gymnotiformes).

The acquisition of elongated, sabre-like canines in multiple vertebrate clades during the last 265 Myr represents a remarkable example for convergent evolution. Due to striking superficial similarities in the cranial skeleton, the same or similar skull and jaw functions have been inferred for sabre-toothed species and interpreted as an adaptation to subdue large-bodied prey. However, although some sabre-tooth lineages have been classified into different ecomorphs (dirk-tooths and scimitar-tooths) the functional diversity within and between groups and the evolutionary paths leading to these specializations are unknown. Here, we use a suite of biomechanical simulations to analyse key functional parameters (mandibular gape angle, bending strength, bite force) to compare the functional performance of different groups and to quantify evolutionary rates across sabre-tooth vertebrates. Our results demonstrate a remarkably high functional diversity between sabre-tooth lineages and that different cranial function and prey killing strategies evolved within clades. Moreover, different biomechanical adaptations in coexisting sabre-tooth species further suggest that this functional diversity was at least partially driven by niche partitioning.

https://royalsocietypublishing.org/doi/pdf/10.1098/rspb.2020.1818

Morphological convergence obscures functional diversity in sabre-toothed carnivores

Disparity, the diversity of form and function of organisms, can be assessed from cladistic or phenetic characters, and from discrete characters or continuous characters such as landmarks, outlines, or ratios. But do these different methods of assessing disparity provide comparable results? Here we provide evidence that all metrics correlate significantly with each other and capture similar patterns of morphological variation. We compare three methods of capturing morphological disparity (discrete characters, geometric morphometric outlines and geometric morphometric landmarks) in coelurosaurian dinosaurs. We standardize our study by focusing all our metrics on the mandible, so avoiding the risk of confounding disparity methods with anatomical coverage of the taxa. The correlation is strongest between the two geometric morphometric methods, and weaker between the morphometric methods and the discrete characters. By using phylogenetic simulations of discrete character and geometric morphometric data sets, we show that the strength of these correlations is significantly greater than expected from the evolution of random data under Brownian motion. All disparity metrics confirm that Maniraptoriformes had the highest disparity of all coelurosaurians, and omnivores and herbivores had higher disparity than carnivores.

/pdf/morphological-disparity-in-theropod-jaws-comparing-discrete-562ywj1aax.pdf

Morphological disparity in theropod jaws: comparing discrete characters and geometric morphometrics

Finite-element (FE) analysis has been used in palaeobiology to assess the mechanical performance of the jaw. It uses two types of models: tomography-based three-dimensional (3D) models (very accura...

/pdf/the-use-of-extruded-finite-element-models-as-a-novel-v1mevhlmt1.pdf

The use of extruded finite-element models as a novel alternative to tomography-based models: a case study using early mammal jaws.

The morphology of the vertebrate lower jaw has been used to infer feeding ecology, with transformations in mandibular shape and structure likely to have facilitated the emergence of different feeding behaviours in vertebrate evolution. Here we present elliptical Fourier shape and principal component analyses, characterizing and comparing the disparity of jaw shape in early gnathostomes and their modern primitively aquatic counterparts. 83% of shape variation is summarized on the first three principal component axes and all component clades of early gnathostomes exhibit overlapping morphological variation. Non-tetrapodomorph Palaeozoic sarcopterygians are more disparate than their extant counterparts whereas extant chondrichthyans are more disparate than their Palaeozoic counterparts. More generally, extant jawed fishes are more disparate than their Palaeozoic relatives largely because of the extensive shape variation exhibited by mandibles of extant actinopterygians. Only some areas of shape space vacated by Palaeozoic gnathostomes have been convergently refilled by living taxa. Characterization of theoretical jaw morphologies demonstrates that fewer than half of all possible shapes are realized by the jawed fishes that comprise our empirical dataset; many of these morphologies are realized by unrepresented terrestrial tetrapods, implying environmental constraint. Our results are incompatible with the early burst model of clade evolution and contradict the hypothesis that maximum disparity is reached early in the evolutionary history of jawed fishes.

/pdf/evolution-of-jaw-disparity-in-fishes-4uzphbjuex.pdf

Evolution of jaw disparity in fishes

The Siluro-Devonian adaptive radiation of jawed vertebrates, which underpins almost all living vertebrate biodiversity, is characterized by the evolutionary innovation of the lower jaw. Multiple lines of evidence have suggested that the jaw evolved from a rostral gill arch, but when the jaw took on a feeding function remains unclear. We quantified the variety of form in the earliest jaws in the fossil record from which we generated a theoretical morphospace that we then tested for functional optimality. By drawing comparisons with the real jaw data and reconstructed jaw morphologies from phylogenetically inferred ancestors, our results show that the earliest jaw shapes were optimized for fast closure and stress resistance, inferring a predatory feeding function. Jaw shapes became less optimal for these functions during the later radiation of jawed vertebrates. Thus, the evolution of jaw morphology has continually explored previously unoccupied morphospace and accumulated disparity through time, laying the foundation for diverse feeding strategies and the success of jawed vertebrates.

https://research-information.bris.ac.uk/ws/files/317063543/sciadv.abl3644.pdf

Jennifer J. Hill

Papers

The use of extruded finite-element models as a novel alternative to tomography-based models: a case study using early mammal jaws.

Evolution of jaw disparity in fishes

Increasing morphological disparity and decreasing optimality for jaw speed and strength during the radiation of jawed vertebrates