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20 results for “evolutionary allometry”
Data from: Australian rodents reveal conserved craniofacial evolutionary allometry across 10 million years of murid evolution
<p>Among vertebrates, placental mammals are particularly variable in the covariance between cranial shape and body size (allometry), with rodents a major exception. Australian murid rodents allow an assessment of the cause of this anomaly because they radiated on an ecologically diverse continent notably lacking other terrestrial placentals. Here we use 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 compared to other rodents, or if conserved allometry suggests intrinsic constraints and/or stabilizing selection. We also assess whether cranial shape variation follows the proposed "rule of craniofacial evolutionary allometry" (CREA), whereby larger species have relatively longer snouts and smaller braincases. To ensure we could differentiate parallel versus non-parallel species-level allometric slopes, we compared the slopes of rarefied samples across all clades. We found exceedingly conserved allometry and CREA-like patterns across the 10 million year split between <i>Mus</i> and Australian murids. This could support both intrinsic constraints and stabilizing selection hypotheses for conserved allometry. Large-bodied frugivores evolved faster than other species along the allometric trajectory, which could suggest stabilizing selection on the shape of the masticatory apparatus as body size changes.</p>
Evolution of static allometry and constraint on evolutionary allometry in a fossil stickleback
<p>Allometric scaling describes the relationship of trait size to body size within and among taxa. The slope of the population-level regression of trait size against body size (<em>i.e., </em>static allometry) is typically invariant among closely related populations and species. Such invariance is commonly interpreted to reflect a combination of developmental and selective constraints that delimit a phenotypic space into which evolution could proceed most easily. Thus, understanding how allometric relationships do eventually evolve is important to understanding phenotypic diversification. In a lineage of fossil Threespine Stickleback (<em>Gasterosteus doryssus</em>), we investigated the evolvability of static allometric slopes for nine traits (five armor, and four non-armor) that evolved significant trait differences across 10 samples over 8,500 years. The armor traits showed weak static allometric relationships and a mismatch between those slopes and observed evolution. This suggests that observed evolution in these traits was not constrained by relationships with body size, perhaps because prior, repeated adaptation to freshwater habitats by Threespine Stickleback had generated strong selection to break constraint. In contrast, for non-armor traits, we found stronger allometric relationships. Those allometric slopes did evolve on short time scales. However, those changes were small and fluctuating and the slopes remained strong predictors of the evolutionary trajectory of trait means over time (<em>i.e.,</em> evolutionary allometry), supporting the hypothesis of allometry as a constraint.</p>
Evolution of static allometry and constraint on evolutionary allometry in a fossil stickleback
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Ecological shifts underlie parallels between ontogenetic and evolutionary allometries in parrotfishes
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Data from: Australian rodents reveal conserved craniofacial evolutionary allometry across 10 million years of murid evolution
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Evolutionary allometry of sexual dimorphism of jumping performance in anurans
<p>Sexual dimorphism is a common feature in animals, yet the degree of sexual dimorphism is not constant across taxa. Sometimes the magnitude of sexual dimorphism varies systematically with body size, resulting in evolutionary allometry of sexual dimorphism. While such patterns are commonly investigated for traits such as overall size, allometric variation in sexual dimorphism of other traits remains underexplored. Here, we characterize the evolutionary allometry of sexual dimorphism in a functional phenotypic trait (jumping performance) in anurans. Using morphology and anatomical approximations of jumping performance across 146 species, we test for evidence of the correlated selection model of sexual dimorphism evolution. We analyze patterns of evolutionary allometry of sexual dimorphism in key phenotypic traits, including: body size (snout-vent length and mass), relative leg length, relative leg muscle volume, mass-specific peak jumping energy, and peak jumping velocity. We find that as previously reported, sexual size dimorphism scales isometrically between species and is independent of sexual dimorphism in jumping performance. Notably, however, we found significant trends in the evolutionary allometry of sexual dimorphism in relative limb length, and in two components of jumping performance. Additionally, we found greater rates of evolution for females versus males in relative limb length, but not jumping performance. We also observed that the allometric trends in limb length dimorphism were related to performance allometry. Sexual dimorphism in jumping performance increased in species with high performance while females in high performance species displayed increased relative limb length. Thus, we hypothesize that selection acting on functional performance explains allometric patterns of sexual dimorphism in morphology. We discuss biological implications of our findings in relation to natural and sexual selection. This study highlights the types of insights one may gain by studying the allometry of sexual dimorphism from a functional perspective to learn about both patterns and processes in evolution.</p>
Data for: Static allometries do not reflect evolutionary allometry in exaggerated weaponry of male New Zealand sheetweb spiders (Cambridgea spp.)
<p>Across the animal kingdom, exaggerated weaponry is frequently used by one sex to contest access for potential mates. Within species, if disproportionate investment in weaponry confers an advantage to larger individuals, this may result in positive static allometry. It is predicted that the same selective pressures may also lead to positive evolutionary allometry, where larger species bear disproportionately large weapons on average, compared with smaller species. However it is unclear whether the slopes of species-specific static allometries are steeper among larger species, or remain consistent. All adult males across the New Zealand sheet-web spider genus Cambridgea bear exaggerated chelicerae which are used to compete for control of females' webs. Here, we characterise the distribution of chelicera lengths within each sex of 12 Cambridgea species to show that chelicerae almost always exhibit positive static allometry in males while female chelicera lengths are consistently isometric. We use comparative phylogenetic methods to demonstrate that the slopes of static allometries steepen in males of larger species but that the ratio of average chelicera length to cephalothorax width is tightly conserved across taxa, leading to an isometric evolutionary allometry. While sexual selection may drive weapon exaggeration within species, resulting in steeper or shallower static allometries, this conservation of relative trait size suggests that chelicera length is subject to other stabilising selective pressures. Changes to species body plans might be constrained, while allowing for disproportionate investment in weapon traits at the extremes of body sizes within species.</p>
Data for: Static allometries do not reflect evolutionary allometry in exaggerated weaponry of male New Zealand sheetweb spiders (Cambridgea spp.)
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Evolutionary allometry of sexual dimorphism of jumping performance in anurans
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Data from: Shell constraints on evolutionary body size-limb size allometry can explain morphological conservatism in the turtle body plan
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Data from: Squamate hatchling size and the evolutionary causes of negative offspring size allometry
Although fecundity selection is ubiquitous, in an overwhelming majority of animal lineages, small species produce smaller number of offspring per clutch. In this context, egg, hatchling and neonate sizes are absolutely larger, but smaller relative to adult body size in larger species. The evolutionary causes of this widespread phenomenon are not fully explored. The negative offspring size allometry can result from processes limiting maximal egg/offspring size forcing larger species to produce relatively smaller offspring ('upper limit'), or from a limit on minimal egg/offspring size forcing smaller species to produce relatively larger offspring ('lower limit'). Several reptile lineages have invariant clutch sizes, where females always lay either one or two eggs per clutch. These lineages offer an interesting perspective on the general evolutionary forces driving negative offspring size allometry, because an important selective factor, fecundity selection in a single clutch, is eliminated here. Under the upper limit hypotheses, large offspring should be selected against in lineages with invariant clutch sizes as well, and these lineages should therefore exhibit the same, or shallower, offspring size allometry as lineages with variable clutch size. On the other hand, the lower limit hypotheses would allow lineages with invariant clutch sizes to have steeper offspring size allometries. Using an extensive data set on the hatchling and female sizes of > 1800 species of squamates, we document that negative offspring size allometry is widespread in lizards and snakes with variable clutch sizes and that some lineages with invariant clutch sizes have unusually steep offspring size allometries. These findings suggest that the negative offspring size allometry is driven by a constraint on minimal offspring size, which scales with a negative allometry.
Data from: The breakdown of static and evolutionary allometries during climatic upheaval
The influence of within-species variation and covariation on evolutionary patterns is well established for generational and macroevolutionary processes, most prominently through genetic lines of least resistance. However, it is not known whether intraspecific phenotypic variation also directs microevolutionary trajectories into the long term when a species is subject to varying environmental conditions. Here we present a continuous, high-resolution bivariate record of size and shape changes among 12,633 individual planktonic foraminifera of a surviving and an extinct-going species over 500 thousand years. This time interval spans the late Pliocene to earliest Pleistocene intensification of Northern Hemisphere glaciation, an interval of profound climate upheaval that can be divided into three phases of increasing glacial intensity. We found that within each of these three Plio-Pleistocene climate phases the within-population allometries predict evolutionary change from one time-step to the next, and that the within-phase among-population (i.e. evolutionary) allometries match their corresponding static (within-population) allometries. However, the evolutionary allometry across the three climate phases deviates significantly from the static and phase-specific evolutionary allometries in the extinct-going species. Although intraspecific variation leaves a clear signature on mean evolutionary change from one time-step to the next, our study suggests that the link between intraspecific variation and longer-term micro- and macroevolutionary phenomena is prone to environmental perturbation that can overcome constraints induced by within-species trait covariation.
Shape coordinates and centroid size for adults and ontogenetic series analyzed in predictable complexity of evolutionary allometry
<p>Allometry has been a paradigm of constraints, including intrinsic constraints on the evolvability of allometry, as a source of developmental and genetic constraints on the evolution of form, and of functional constraints, maintaining functional equivalence as body size evolves. Yet, allometry may be the simplest case of varied constraints, and of morphological integration, even though allometry itself is not simple. Evolutionary allometry may be especially complex because it depends not only on the developmental origins of allometry and determinants of allometric variation but also on the evolutionary dynamics of size and shape. It should also depend on the ecological opportunity for size-dependent ecomorphological specialization. We predict that lineages that converge in those would exhibit similar evolutionary allometries but otherwise, evolutionary allometries would be heterogeneous. Countering this expectation are familiar craniofacial evolutionary allometries, often ascribed to developmental bias. To test both those hypotheses, we compare evolutionary allometries of mandibles across lineages of squirrels and evolutionary to growth allometries. As expected, lineages that converge on size-dependent specializations exhibit similar evolutionary allometries, but otherwise, their allometries are no more similar than expected by chance. Growth allometries of squirrels (and a cricetid rodent) slightly resemble the evolutionary allometry of one lineage, but growth allometries of species from other lineages are orthogonal to their own lineages' evolutionary allometry. We would expect that craniofacial allometries that are not brain-driven would, like mandibular evolutionary allometries, be predictable only from size-dependent ecological specializations.</p>
Data from: The breakdown of static and evolutionary allometries during climatic upheaval
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A highly conserved ontogenetic limb allometry and its evolutionary significance in the adaptive radiation of Anolis lizards
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Data from: Squamate hatchling size and the evolutionary causes of negative offspring size allometry
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Shape coordinates and centroid size for adults and ontogenetic series analyzed in predictable complexity of evolutionary allometry
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Data from: Evolutionary covariation in geometric morphometric data: analyzing integration, modularity, and allometry in a phylogenetic context
Quantifying integration and modularity of evolutionary changes in morphometric traits is crucial for understanding how organismal shapes evolve. For this purpose, comparative studies are necessary, which need to take into account the phylogenetic structure of interspecific data. This study applies several of the standard tools of geometric morphometrics, which mostly have been used in intraspecific studies, in the new context of analyzing integration and modularity based on comparative data. Morphometric methods such as principal component analysis, multivariate regression, partial least squares and modularity tests can be applied to phylogenetically independent contrasts of shape data. We illustrate this approach in an analysis of cranial evolution in 160 species from all orders of birds. Mapping the shape information onto the phylogeny indicates that there is a significant phylogenetic signal in skull shape. Multivariate regression of independent contrasts of shape on independent contrasts of size reveals clear evolutionary allometry. Regardless of whether or not a correction for allometry is used, evolutionary integration between the face and braincase is strong, and tests reject the hypothesis that the face and braincase are separate evolutionary modules. These analyses can easily be applied to other taxa and can be combined with other morphometric tools to address a wide range of questions about evolutionary patterns and processes.
Data from: Evolutionary covariation in geometric morphometric data: analyzing integration, modularity, and allometry in a phylogenetic context
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Supplementary material to: Segmental series and size: clade-wide investigation of molar proportions reveals a major evolutionary allometry in the dentition of placental mammals
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Annotated Behaviour and Observability Dataset (ABODe)
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