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129 results for “developmental plasticity”
Variation in personality shaped by evolutionary history, genotype, and developmental plasticity in response to feeding modalities in the Arctic charr
<p>Animal personality has been shown to be influenced by both genetic and environmental factors and shaped by natural selection. Currently, little is known about mechanisms influencing the development of personality traits. This study examines the extent to which personality development is genetically influenced and/or environmentally responsive (plastic). We also investigated the role of evolutionary history, assessing whether personality traits could be canalized along a genetic and ecological divergence gradient. We tested the plastic potential of boldness in juveniles of five Icelandic Arctic charr morphs (<em>Salvelinus</em> <em>alpinus</em>), including two pairs of sympatric morphs, displaying various degrees of genetic and ecological divergence from the ancestral anadromous charr, split between treatments mimicking benthic vs. pelagic feeding modalities. We show that differences in mean boldness are mostly affected by genetics. While the benthic treatment led to bolder individuals overall, the environmental effect was rather weak, suggesting that boldness lies under strong genetic influence with reduced plastic potential. Finally, we found hints of differences by morphs in boldness canalization through reduced variance and plasticity, and higher consistency in boldness within morphs. These findings provide new insights into how behavioural development may impact adaptive diversification.</p>
Developmental bias in the evolution and plasticity of beetle horn shape
<p>The degree to which developmental systems bias the phenotypic effects of environmental and genetic variation, and how these biases affect evolution, is subject to much debate. Here, we assess whether developmental variability in horn shape aligns with the phenotypic effects of plasticity and evolutionary divergence, yielding three salient results. First, we find that most pathways previously shown to regulate horn length also affect shape. Second, we find that the phenotypic effects of manipulating divergent developmental pathways are correlated with each other as well as multivariate fluctuating asymmetry – a measure of developmental variability. Third, these effects further aligned with thermal plasticity, population differences, and macroevolutionary divergence between sister taxa and more distantly related species. Collectively, our results support the hypothesis that changes in horn shape —whether brought about by environmentally plastic responses, functional manipulations, or evolutionary divergences— converge along 'developmental lines of least resistance', i.e., are biased by the developmental system underpinning horn shape.</p>
Data for: Associations between leaf developmental stability, canalization and phenotypic plasticity in an architectural perspective
<p class="MsoNormal"><span>Associations between developmental stability, canalization and phenotypic plasticity have been predicted, but rarely supported by direct evidence. Architectural analysis may provide a more powerful approach to finding correlations among these mechanisms in plants. T</span><span>o investigate the relationships among the three mechanisms in architectural perspective, w</span><span>e </span><span>subjected plants of </span><em><span>Abutilon theophrasti</span></em><span> to three densities, measured and calculated </span><span>fluctuating asymmetry (FA), coefficients of variation (CV)</span><span> and </span><span>plasticity (PI) of three leaf traits, to analyze the </span><span>correlations among these variables.</span><span> As density increased, mean leaf size, petiole length and angle of most layers and mean leaf FA of some layers decreased (at both stages), CV of petiole angle increased (at day 50), and PI of petiole length and angle across all layers decreased (at day 70); leaf FA and CV of traits generally increased with higher layers at all densities. At both stages, there were more positive correlations between FA and CV at lower vs. high densities; at day 50, little correlation of plasticity with FA or CV was found; at day 70, more positive correlations between FA and PI occurred for response to high vs. low density than for response to medium vs. low density, and more positive correlations between CV and PI occurred at lower vs. high densities. Results suggested that developmental instability, decreased canalization and plasticity can be cooperative and the relationships between decreased canalization and plasticity are more likely to be positive if decreased canalization is due to vibrant growth rather than stressful effects. The relationships of plasticity with developmental instability differed from its relationship with decreased canalization in the way of variation. Decreased canalization should be more beneficial for possible plasticity in the future, while canalization may result from already-expressed plasticity.</span></p>
Can developmental plasticity shape sexual competition and promote reproductive isolation?
<p>Environmental factors such as dietary nutrients can shape the expression of developmentally plastic sexual traits in many species. However, while there has been extensive research into the developmental plasticity of sexual traits at the individual level, the broader consequences of this variation at the population scale remain poorly understood. Here, we asked whether plastic responses to the developmental environment can shape sexual competition and initiate reproductive isolation between populations. We reared neriid flies, <em>Telostylinus angusticollis</em>,<em> </em>on nutrient-rich and nutrient-poor larval diets, generating adult flies that differed in body size and secondary sexual trait expression. We then investigated sexual competition in experimental populations from each developmental environment, and tested for reproductive isolation between flies from mismatched environments. We found that, compared with poor-diet populations, rich-diet populations exhibited more frequent and escalated male-male combat and more frequent mating and mate-guarding. However, we found no evidence that sexual selection was affected by the developmental environment. Mismatched female-male pairs tended to take longer to mate and rich-diet females often rejected poor-diet males, but mismatched pairs were not less likely to mate within 1 hour or produce viable offspring. Our findings suggest that developmental plasticity could generate dramatic differences in sexual competition between populations, and could contribute to reproductive isolation.</p>
Figure 9 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 9. Phylogenetic relationships within Eryopidae as found in the present analysis, with the most important synapomorphies mapped onto nodes. See Appendix A for character definitions and a matrix, and see the text for a complete list of results.
Figure 8 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 8. Morphometrics of eryopiform skulls, depicting crucial skull proportions relative to size. Arrows in (a) highlight ontogeny in O. labyrinthicus and S. haeuseri.
Figure 6 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 6. Cranial morphology in eryopid temnospondyls, exemplified by reconstructed skull dorsal views. (a) Actinodon frossardi (after Werneburg, 1997), (b) Osteophorus roemeri (after Meyer, 1860), (c) Glaukerpeton avinoffi (after Werneburg and Berman, 2012), (d) Onchiodon labyrinthicus (after Boy, 1990), (e) Onchiodon thuringiensis (after Werneburg, 2008), (f) Clamorosaurus nocturnus (after Gubin, 1983, and photographs courteously provided by Ralf Werneburg), (g) Eryops sp. from the Moran Formation (MCZ 1914), (h) Eryops anatinus (AMNH 4310), (i) Eryops megacephalus (MCZ 1129). Darker shading figures depressions on the dorsal side of the skull roof.
Figure 7 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 7. Morphospace occupation of eryopiform skulls, showing differences in ontogenetic change and morphometric variance between Onchiodon labyrinthicus and Sclerocephalus spp. and adult skulls of other eryopids. (a) PC1–PC2 axes, (b) areas occupied by immature Onchiodon and Sclerocephalus compared, (c) close-up of (a) with focus on variation in O. labyrinthicus, and (d) PC1 plotted against size.
Figure 2 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 2. Larger juveniles of Onchiodon labyrinthicus Geinitz. (a) LFUG 13570, (b) LFUG 13501, (c) MMG SaP 356, (d) LFUG 13391, (e) LFUG 13398, (f) LFUG 13609, (g) LFUG 13047. Darker shading figures depressions on the dorsal side of the skull roof. Scale equals 10 mm.
Figure 4 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 4. Reconstruction of skulls in dorsal view Onchiodon labyrinthicus Geinitz. (a) MMG SaP 237, (b) LFUG 13343, (c) LFUG 13405, (d) MMG SaP 356, (e) LFUG 13391, (f) LFUG 13570, (g) LFUG 13501, (h) LFUG 13292. Darker shading figures depressions on dorsal side of skull roof. Scale equals 10 mm.
Figure 5 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 5. Palate of Onchiodon labyrinthicus Geinitz, in ventral view. (a) LFUG 13394, (b) LFUG 13514. Darker grey is the inner side of the skull roof. Scale equals 10 mm.
Figure 3 in The life cycle in late Paleozoic eryopid temnospondyls: developmental variation, plasticity and phylogeny
Figure 3. Ontogeny of the dermal ornament in Onchiodon labyrinthicus Geinitz. (a) LFUG 13343, (b) MMG SaP 390, (c) MMG SaP 356, (d) MMG SaP 361, (e) LFUG 13395, (f) LFUG 13391, (g) LFUG 13570, (h) LFUG 13292.
Main dataset 'Environmental specificity in Drosophila-bacteria symbiosis affects host developmental plasticity'
<p>Main dataset from the manuscript 'Environmental specificity in <em>Drosophila</em>-bacteria symbiosis affects host developmental plasticity' (2019)</p>
MANOVA dataset 'Environmental specificity in Drosophila-bacteria symbiosis affects host developmental plasticity'
<p>MANOVA dataset from the manuscript 'Environmental specificity in <em>Drosophila</em>-bacteria symbiosis affects host developmental plasticity' (2019)</p>
Variation in personality shaped by evolutionary history, genotype, and developmental plasticity in response to feeding modalities in the Arctic charr
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Comparison of thermal developmental plasticity among seven recently sympatric <i>Anolis</i> species: insights into the evolution of reaction norms
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Data for: Associations between leaf developmental stability, canalization and phenotypic plasticity in an architectural perspective
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Data and analyses from: Context matters: A meta-analysis of the variable impacts of transgenerational and developmental plasticity on responses to stress
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Data from: Developmental behavioural plasticity and DNA methylation patterns in response to predation stress in Trinidadian guppies
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Developmental bias in the evolution and plasticity of beetle horn shape
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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