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Guillerme, T.

Publications and source records attributed to Guillerme, T..

11 recordsLinked to original sources

Disparity analyses are robust to ancestral state estimation uncertainty

Morphological trait datasets and phylogenies are routinely paired to investigate macroevolutionary patterns during disparity analyses. However, incomplete fossil sampling can distort disparity estimates, obscuring true evolutionary signals. Ancestral state estimation can be used for both continuous and discrete traits to extend these analyses beyond incomplete fossil data, such as investigations into disparity through time. However, when ancestral state estimation occurs in the disparity pipeline, and the inevitable uncertainty in these estimates, complicate their integration. Determining the most robust workflow for integrating ancestral state estimation in disparity analyses remains a critical methodological challenge. Using simulations to attain a ground-truth disparity value, we evaluated different approaches to performing ancestral state estimation and incorporating uncertainty across varying continuous and discrete trait models, fossil sampling densities and disparity metrics. Ancestral state estimation generally improved recovery of true disparity relative to tip-only analyses, though the optimal approach depended on the interaction between trait model and fossil sampling density. For continuous traits, probabilistic approaches were most accurate, but were sensitive to model misspecification under low fossil sampling density. For discrete traits, pre-ordination methods were most reliable and probabilistic approaches outperformed point estimates under low sampling, while point estimates became increasingly accurate as sampling density increased. Fossil sampling density was a stronger predictor of disparity accuracy than estimation method choice, underscoring that methodologies are only as powerful as the data provided. Our findings offer a practical decision framework for selecting the most appropriate workflow given the sampling density and trait characteristics of a dataset.

evolutionary biology↗

The what, how and why of trait-based analyses in ecology

Functional diversity is increasingly used alongside taxonomic diversity to describe populations and communities in ecology. Indeed, functional diversity metrics allow researchers to summarize complex occupancy patterns in space and/or time (what is changing?) that lead to changes in communities and/or populations (the process; how is it changing?) in response to some stressors (the mechanism; why is it changing?). However, as the diversity of functional diversity metrics and methods increases, it is often not directly clear which metric is more readily appropriate for which question. We studied the ability of different functional diversity metrics to recover patterns and signals from different processes linked to common assembly mechanisms (environmental filtering, competitive exclusion, equalizing fitness, and facilitation) in community ecology. Using both simulated data and an empirical dataset affected by more complex and nuanced mechanisms, we tested the effectiveness of different space occupancy metrics to recover the simulated or empirical changes. We show that different metrics perform better for different tasks, emphasizing the importance of not using a one-size-fits-all metric. Instead, researchers should carefully consider and test whether a particular metric will be effective in capturing a pattern of interest.

ecology↗

Evolutionary dynamics of pigmentary grey and non- iridescent structural blue colouration in Tanagers (family: Thraupidae)

3.1Birds are one of the most colourful animal groups in the world and there are multiple ways by which they achieve this feature. Mechanisms of colour production range from pigmentary (pigment deposition) to structural (nanostructural arrangements), or the combination of both. Despite the huge breadth of colour gamut, the basic components of feathers are shared across all of them (keratin, air and presence of pigments in accordance with the colour produced). It has been shown that in some instances, colour evolution between pigmentary and structural colours can proceed by rearrangement of the nano-structural elements of feathers. Here, we investigated evolutionary transitions between pigmentary grey and non-iridescent structural blue. We focus on the Thraupidae (tanagers and allies) that display a variety of blues and greys including a potential transition state that we refer to as slate. We used digitally calibrated images of birds to quantify colour and determine the distinctiveness of slate colour in colourspace. Following, we identify the most likely pathway for the evolution of the colour blue: from grey via slate colour. Our research reveals a new pathway in the evolution of blue colour.

evolutionary biology↗

Calculating functional diversity metrics using neighbor-joining trees

O_LIThe study of functional diversity (FD) provides ways to understand phenomena as complex as community assembly or the dynamics of biodiversity change under multiple pressures. Different frameworks are used to quantify FD, either based on dissimilarity matrices (e.g., Rao entropy, functional dendrograms) or multidimensional spaces (e.g. convex hulls, kernel-density hypervolumes). While the first does not enable the measurement of FD within a richness/divergence/regularity framework, or results in the distortion of the functional space, the latter does not allow for comparisons with phylogenetic diversity (PD) measures and can be extremely sensitive to outliers. C_LIO_LIWe propose the use of neighbor-joining trees (NJ) to represent and quantify functional diversity in a way that combines the strengths of current FD frameworks without many of their weaknesses. Our proposal is also uniquely suited for studies that compare FD with PD, as both share the use of trees (NJ or others) and the same mathematical principles. C_LIO_LIWe test the ability of this novel framework to represent the initial functional distances between species with minimal functional space distortion and sensitivity to outliers. The results using NJ are compared with conventional functional dendrograms, convex hulls, and kernel-density hypervolumes using both simulated and empirical datasets. C_LIO_LIUsing NJ we demonstrate that it is possible to combine much of the flexibility provided by multidimensional spaces with the simplicity of tree-based representations. Moreover, the method is directly comparable with PD measures, and enables quantification of the richness, divergence and regularity of the functional space. C_LI

ecology↗

Innovation and elaboration on the avian tree of life

1Widely documented, megaevolutionary jumps in phenotypic diversity continue to perplex researchers because it remains unclear whether these dramatic changes can emerge from microevolutionary processes. Here we tackle this question using new approaches for modeling multivariate traits to evaluate the magnitude and distribution of elaboration and innovation in the evolution of bird beaks. We find that elaboration, evolution along the major axis of phenotypic change, is common at both macro- and megaevo-lutionary scales whereas innovation, evolution away from the major axis of phenotypic change, is more prominent at megaevolutionary scales. Indeed, the major axis of phenotypic change among species beak shapes at megaevolutionary scales is an emergent property of innovation across clades. Our analyses suggest that the reorientation of phenotypes via innovation is a ubiquitous route for divergence that can arise through gradual change alone, opening up new avenues for evolution to explore.

evolutionary biology↗

Endochondral bone in an Early Devonian 'placoderm' from Mongolia

Endochondral bone is the main internal skeletal tissue of nearly all osteichthyans--the group comprising more than 60,000 living species of bony fishes and tetrapods. Chondrichthyans (sharks and their kin) are the living sister group of osteichthyans and have cartilaginous endoskeletons, long considered the ancestral condition for all jawed vertebrates (gnathostomes). The absence of bone in modern jawless fishes and the absence of endochondral ossification in early fossil gnathostomes appears to lend support to this conclusion. Here we report the discovery of extensive endochondral bone in Minjinia turgenensis, a new genus and species of placoderm-like fish from the Early Devonian (Pragian) of western Mongolia described using x-ray computed microtomography (XR-{micro}CT). The fossil consists of a partial skull roof and braincase with anatomical details providing strong evidence of placement in the gnathostome stem group. However, its endochondral space is filled with an extensive network of fine trabeculae resembling the endochondral bone of osteichthyans. Phylogenetic analyses place this new taxon as a proximate sister group of the gnathostome crown. These results provide direct support for theories of generalised bone loss in chondrichthyans. Furthermore, they revive theories of a phylogenetically deeper origin of endochondral bone and its absence in chondrichthyans as a secondary condition.

paleontology↗

Australian rodents reveal conserved Cranial Evolutionary Allometry across 10 million years of murid evolution

Among vertebrates, placental mammals are particularly variable in the covariance between their cranial shapes and body size (allometry), with the notable exception of rodents. Australian murid rodents present an opportunity to assess the cause of this anomaly because they radiated on an ecologically diverse continent unique for lacking other terrestrial placentals. Here we used 3D geometric morphometrics to quantify species-level and evolutionary allometries in 38 species (317 crania) from all Australian murid genera. We ask if ecological opportunity resulted in greater allometric diversity; conversely, we test if intrinsic constraints and/or stabilizing selection conserved allometry. To increase confidence in species-level allometric slopes, we introduce a new phylogeny-based method of bootstrapping and randomly resampling across the whole sample. We found exceedingly conserved allometry across the 10 million year split between Mus and the clade containing Australian murids. Cranial shapes followed craniofacial evolutionary allometry (CREA) patterns, with larger species having relatively longer snouts and smaller braincases. CREA is consistent with both intrinsic constraints and stabilizing selection hypotheses for conserved allometry. However, large-bodied frugivores evolved faster, while carnivorous specialists showed skull modifications known to conflict with masticatory efficiency. These results suggest a strong role of stabilizing selection on the masticatory apparatus of murid rodents.

evolutionary biology↗

Shifting spaces: which disparity or dissimilarity metrics best summarise occupancy in multidimensional spaces?

O_LIMultidimensional analysis of traits are now a common toolkit in ecology and evolution and are based on trait-spaces in which each dimension summarise the observed trait combination (a morphospace or an ecospace). Observations of interest will typically occupy a subset of this trait-space, and researchers will apply one or more metrics to quantify the way in which organisms \"inhabit\" that trait-space. In macroevolution and ecology these metrics are referred to as disparity or dissimilarity metrics and can be generalised as space occupancy metrics. Researchers use these metrics to investigate how space occupancy changes through time, in relation to other groups of organisms, and in response to global environmental changes, such as global warming events or mass extinctions. However, the mathematical and biological meaning of most space occupancy metrics is vague with the majority of widely-used metrics lacking formal description.\nC_LIO_LIHere we propose a broad classification of space occupancy metrics into three categories that capture changes in volume, density, or position. We analyse the behaviour of 25 metrics to study changes in trait-space volume, density and position on a series of simulated and empirical datasets.\nC_LIO_LIWe find no one metric describes all of trait-space but that some metrics are better at capturing certain aspects compared to other approaches and that their performance depends on both the trait-space and the hypothesis analysed. However, our results confirm the three broad categories (volume, density and position) and allow to relate changes in any of these categories to biological phenomena.\nC_LIO_LISince the choice of space occupancy metric should be specific to the data and question at had, we introduced moms, a user-friendly tool based on a graphical interface that allows users to both visualise and measure changes space occupancy for any metric in simulated or imported trait-spaces. Users are also provided with tools to transform their data in space (e.g. contraction, displacement, etc.). This tool is designed to help researchers choose the right space occupancy metrics, given the properties of their trait-space and their biological question.\nC_LI

evolutionary biology↗

Individual variation of the masticatory system dominates 3D skull shape in the herbivory-adapted marsupial wombats

BackgroundWithin-species skull shape variation of marsupial mammals is widely considered low and strongly size-dependent (allometric), possibly due to developmental constraints arising from the altricial birth of marsupials. However, species whose skulls are impacted by strong muscular stresses - particularly those produced through mastication of tough food items - may not display such intrinsic patterns very clearly because of the known plastic response of bone to muscle activity of the individual. In such cases, shape variation should not be dominated by allometry; ordination of shape in a geometric morphometric context through principal component analysis (PCA) should reveal main variation in areas under masticatory stress (incisor region/zygomatic arches/mandibular ramus); but this main variation should emerge from high individual variability and thus have low eigenvalues.\n\nResultsWe assessed the evidence for high individual variation through 3D geometric morphometric shape analysis of crania and mandibles of thre species of grazing-specialized wombats, whose diet of tough grasses puts considerable strain on their masticatory system. As expected, we found little allometry and low Principal Component 1 (PC1) eigenvalues within crania and mandibles of all three species. Also as expected, the main variation was in the muzzle, zygomatic arches, and masticatory muscle attachments of the mandibular ramus. We then implemented a new test to ask if the landmark variation reflected on PC1 was reflected in individuals with opposite PC1 scores and with opposite shapes in Procrustes space. This showed that correspondence between individual and ordinated shape variation was limited, indicating high levels of individual variability in the masticatory apparatus.\n\nDiscussionOur results are inconsistent with hypotheses that skull shape variation within marsupial species reflects a constraint pattern. Rather, they support suggestions that individual plasticity can be an important determinant of within-species shape variation in marsupials (and possibly other mammals) with high masticatory stresses, making it difficult to understand the degree to which intrinsic constraint act on shape variation at the within-species level. We conclude that studies that link micro- and macroevolutionary patterns of shape variation might benefit from a focus on species with low-impact mastication, such as carnivorous or frugivorous species.

evolutionary biology↗

Influence of different modes of morphological character correlation on phylogenetic tree inference

Phylogenetic analysis algorithms require the assumption of character independence - a condition generally acknowledged to be violated by morphological data. Correlation between characters can originate from intra-organismal features, shared phylogenetic history or forced by particular character-state coding schemes. Although the two first sources can be investigated by biologists a posteriori and the third one can be avoided a priori with good practices, phylogenetic software do not distinguish between any of them.\n\nIn this study, we propose a new metric of raw character difference as a proxy for character correlation. Using thorough simulations, we test the effect of increasing or decreasing character differences on tree topology. Overall, we found an expected positive effect of reducing character correlations on recovering the correct topology. However, this effect is less important for matrices with a small number of taxa (25 in our simulations) where reducing character correlation is not more effective than randomly drawing characters. Furthermore, in bigger matrices (350 characters), there is a strong effect of the inference method with Bayesian trees being consistently less affected by character correlation than maximum parsimony trees.\n\nThese results suggest that ignoring the problem of character correlation or independence can often impact topology in phylogenetic analysis. However, encouragingly, they also suggest that, unless correlation is actively maximised or minimised, probabilistic methods can easily accommodate for a random correlation between characters.

evolutionary biology↗

Morphological phylogenetic analysis with inapplicable data

Non-independence of characters is a real phenomenon in phylogenetic data matrices, even though phylogenetic reconstruction algorithms generally assume character independence. In morphological datasets, the problem results in characters that cannot be applied to certain terminal taxa, with this inapplicability treated as \"missing data\" in a popular method of character coding. However, this treatment is known to create spurious tree length estimates on certain topologies, potentially leading to erroneous results in phylogenetic searches. Here we present a single-character algorithm for ancestral states reconstruction in datasets that have been coded using reductive coding. The algorithm uses up to four traversals on a tree to resolve final ancestral states - which are required in full before a tree can be scored. The algorithm employs explicit criteria for the resolution of ambiguity in applicable/inapplicable dichotomies and the optimization of missing data. We score trees following a previously published procedure that minimizes homoplasy over all characters. Our analysis of published datasets shows that, compared to traditional methods, our new method identifies different trees as \"optimal\"; as such, correcting for inapplicable data may significantly alter the outcome of tree searches.

evolutionary biology↗