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70 results for “wing shape”
Active shape programming drives Drosophila wing disc eversion
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Evolutionary constraints shape the diversity of microinsects' wing morphology
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Data from: From 20 to 2? Landmark-based geometric morphometrics reveal negligible wing-shape divergence between 20 subspecies of the Apollo butterfly, Parnassius apollo (Lepidoptera, Papilionidae), in the Carpatho-Pannonian region
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Overlap in the wing shape of migratory, nomadic and sedentary grass parrots
Bird wing shape is highly correlated with mobility, and vagile species have more pointed wing tips than sedentary ones. Most studies of bird wing shape are biased to the northern hemisphere, and consider only two migratory syndromes (north-south migrants or sedentary species). There are major gaps in knowledge about the wing shapes of different taxa with other movement strategies (e.g. nomads) in the southern hemisphere. Parrots are a prominent southern hemisphere bird order with complex movement patterns, but their wing shapes are mostly unstudied. We test whether three metrics of wing shape of grass parrots (Neophema and Neopsephotus spp.) correspond to their purported migration syndromes (and other factors). We show that two strongly migratory grass parrots and an arid-adapted nomad had pointed wings, with flight feather longer distally and shorter proximally. However, purportedly sedentary species overlapped extensively with migrants and nomads in all aspects of wing shape, and taxonomic relationships, purported migratory syndromes and ecological barriers did not explain the variation we recorded. The most distantly related species (Neopsephotus) had most dissimilar wing shape to the others, but broadly conformed to the expectations of long pointed wings of a nomad. Why purportedly sedentary grass parrots had unexpectedly pointed wings is unclear. We propose the hypothesis that this wing shape may persist in sedentary populations if individuals experience strong but intermittent selection to disperse when environmental conditions are poor. If pointed wings are not costly during good times when individuals are sedentary, this wing shape may persist in populations as a 'back up' in bad times. Our study highlights the interesting migration patterns in the southern hemisphere that remain largely unstudied. Wing shape offers an interesting way to identify potentially undiscovered capacity for movement in data deficient species, which may also have implications for conservation.
Data from: Local and landscape-scale heterogeneity shape spotted wing drosophila (Drosophila suzukii) activity and natural enemy abundance: implications for trophic interactions
Like natural enemies, invasive polyphagous pests may respond positively to local and landscape-scale diversity, making them more serious challenges to sustainable management than specialists. Yet the current view of landscape effects on pests rarely considers perennial systems or polyphagous pests. We investigated Drosophila suzukii (SWD) and natural enemy distributions and trophic interactions in blueberry systems of the southeast US in relation to local management and landscape structure. Fields were nested in 1-km landscapes along gradients of crop and forest heterogeneity (landscape compositional diversity) and field border and crop border lengths (landscape configurational diversity). Yeast-sugar bait traps were used to collect SWD and canopy suction sampling for natural enemies. Management practices at the local scale did not influence SWD abundance, but natural enemy abundance was higher in organic systems and fields with vegetation present between rows. Landscape configurational diversity and greater proportion of non-cropping habitat promoted higher SWD populations. Natural enemy communities were composed of highly generalized species, and contrary to our predictions, we observed lower abundances in landscapes with higher proportion of non-cropping area. Few predators were detected to have fed on SWD, and communities were dominated by predators with low specialization on prey in blueberry. Our results indicate that local and landscape features in blueberry landscapes have differential effects on a polyphagous pest and generalist natural enemies. Our initial analysis of predator diets, using a metabarcoding approach, suggests spatial structure in specialization on prey with high diversity of prey in predators collected in forested margins.
Data from: Evolution of wing shape in hornets: why is the wing venation efficient for species identification?
Wing venation has long been used for insect identification. Lately, the characterization of venation shape using geometric morphometrics has further improved the potential of using the wing for insect identification. However, external factors inducing variation in wing shape could obscure specific differences, preventing accurate discrimination of species in heterogeneous samples. Here, we show that interspecific difference is the main source of wing shape variation within social wasps. We found that a naive clustering of wing shape data from taxonomically and geographically heterogeneous samples of workers returned groups congruent with species. We also confirmed that individuals can be reliably attributed to their genus, species and populations on the basis of their wing shape. Our results suggested that the shape variation reflects the evolutionary history with a potential influence of other factors such as body shape, climate and mimicry selective pressures. However, the high dimensionality of wing shape variation may have prevented absolute convergences between the different species. Wing venation shape is thus a taxonomically relevant marker combining the accuracy of quantitative characters with the specificity required for identification criteria. This marker may also highlight adaptive processes that could help understand the wing's influence on insect flight.
Data from: Wing shape variation associated with mimicry in butterflies
Mimetic resemblance in unpalatable butterflies has been studied by evolutionary biologists for over a century, but has largely focused on the convergence in wing color patterns. In Heliconius numata, discrete color-pattern morphs closely resemble co-mimics in the distantly-related genus Melinaea. We examine the possibility that the shape of the butterfly wing also shows adaptive convergence. First, simple measures of forewing dimensions were taken of individuals in a cross between H. numata morphs, and showed quantitative differences between two of the segregating morphs, F. elegans and F. silvana. Second, landmark-based geometric morphometric and elliptical Fourier outline analyses were used to more fully characterize these shape differences. Extension of these techniques to specimens from natural populations suggested that, while many of the coexisting morphs could not be discriminated by shape, the differences we identified between F. elegans and F. silvana hold in the wild. Interestingly, despite extensive overlap, the shape variation between these two morphs is paralleled in their respective Melinaea co-mimics. Our study therefore suggests that wing-shape variation is associated with mimetic resemblance, and raises the intriguing possibility that the supergene responsible for controlling the major switch in color pattern between morphs also contributes to wing shape differences in H. numata.
Data from: Genetic and morphological variation in sexual and asexual parasitoids of the genus Lysiphlebus: an apparent link between wing shape and reproductive mode
Background Endoparasitoids of aphids belonging to the genus Lysiphlebus Foerster (Hymenoptera: Braconidae: Aphidiinae) comprise over 20 species that exploit over a hundred species of aphid hosts including many important pest aphid species. Within the genus Lysiphlebus two genetically and morphologically well defined species groups are recognized: the "fabarum" and the "testaceipes" group both including taxa with sexual (arrhenotoky) and asexual (thelytoky) reproduction modes. However the diverse patterns of morphological variation which include clearly distinguishable morphotypes and genetic variation within species groups are not yet resolved. To address the relationship between morphological evolution and genetic divergence in Lysiphlebus wasps we explored both genetic differentiation (mitochondrial and nuclear gene sequences) and morphological variation (wing size and shape) and the changes in wing size and shape in the phylogenetic context. Results and Discussion Analyses of mitochondrial and nuclear gene sequences determine the separation of the genus into two species groups ("testaceipes" and "fabarum" groups) revealed three well defined phylogenetic lineages within "fabarum" species group including yet undefined species. Mapping wing shape data onto molecular phylogenetic indicated that the concordance between genetic diversification and divergence in the wing shape results from the deep split between two main species group. No association between pattern of genetic diversification morphotypes and wing shape variation within species groups was observed. The clear association between wing shape and reproductive mode was the most surprising result of our study. We propose two possible mutually non-exclusive mechanisms which may explain the link between reproductive mode and the shape of the wing Conclusions Combining molecular analysis with analysis of wing shape allows us determining existence of one cryptic yet undescribed species. At the same time we determine that Lysiphlebus fabarum group need detailed taxonomic revision because species boundaries as defined cannot be upheld. Mapping wing shape onto independently derived molecular phylogeny revealed that deep genetic divergence is associated with evolutionary changes in wing shape of Lysiphlebus wasps. Among most recently diverged taxa the morphological variation in the wing shape can be explained by the reproduction mode.
Data from: Cryptic differences in colour among Müllerian mimics: how can the visual capacities of predators and prey shape the evolution of wing colours?
Antagonistic interactions between predators and prey often lead to co-evolution. In the case of toxic prey, aposematic colours act as warning signals for predators and play a protective role. Evolutionary convergence in colour patterns among toxic prey evolves due to positive density-dependent selection and the benefits of mutual resemblance in spreading the mortality cost of educating predators over a larger prey assemblage. Comimetic species evolve highly similar colour patterns, but such convergence may interfere with intraspecific signalling and recognition in the prey community, especially for species involved in polymorphic mimicry. Using spectrophotometry measures, we investigated the variation in wing coloration among comimetic butterflies from distantly related lineages. We focused on seven morphs of the polymorphic species Heliconius numata and the seven corresponding comimetic species from the genus Melinaea. Significant differences in the yellow, orange and black patches of the wing were detected between genera. Perceptions of these cryptic differences by bird and butterfly observers were then estimated using models of animal vision based on physiological data. Our results showed that the most strikingly perceived differences were obtained for the contrast of yellow against a black background. The capacity to discriminate between comimetic genera based on this colour contrast was also evaluated to be higher for butterflies than for birds, suggesting that this variation in colour, likely undetectable to birds, might be used by butterflies for distinguishing mating partners without losing the benefits of mimicry. The evolution of wing colour in mimetic butterflies might thus be shaped by the opposite selective pressures exerted by predation and species recognition.
Fig. 8 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)
Fig. 8 The distribution of the wing venation types relative to the species mean sizes (log centroid size). The phylogeny is superimposed according to the reconstructed ancestral values. The character states are colourcoded same as in the Fig. 5
Fig. 7 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)
Fig. 7 Shape changes associated with the first three PCs are shown as extreme wing shapes (black shape) representing the shape of species with maximal positive and negative score of each axis comparing to the mean shape of the sample (grey shape)
Fig. 4 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)
Fig. 4 Wing venation types in Aphidiinae and number of character state changes. Distribution of veins and cells in the medial and distal part of the wing were considered, as proximal part of the wing has the same structure in all Aphidiinae. a Four cells type. b Fork type. c Axe stigma type. d H letter type. e Horse head type. f Hook type. The changes in venation are highlighted in red and marked by smaller arrows
Fig. 1 in Evolutionary relationships of wing venation and wing size and shape in Aphidiinae (Hymenoptera: Braconidae)
Fig. 1 Diversity of wing types characterized by the presence/ absence of wing veins and cells. a Ephedrus plagiator. b Pseudephedrus sp.. c Praon barbatum. d Lysiphlebus fabarum. e Aphidius ervi. f Binodoxys angelicae. Detailed wing type definition is given in the text
Data from: Wing shape variation associated with mimicry in butterflies
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Data from: Evolution of wing shape in hornets: why is the wing venation efficient for species identification?
Open the record for dataset details and reuse information.
Data from: Local and landscape-scale heterogeneity shape spotted wing drosophila (Drosophila suzukii) activity and natural enemy abundance: implications for trophic interactions
Open the record for dataset details and reuse information.
Overlap in the wing shape of migratory, nomadic and sedentary grass parrots
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Data from: Antagonistic natural and sexual selection on wing shape in a scrambling damselfly
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Data from: Cryptic differences in colour among Müllerian mimics: how can the visual capacities of predators and prey shape the evolution of wing colours?
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Data from: Genetic and morphological variation in sexual and asexual parasitoids of the genus Lysiphlebus: an apparent link between wing shape and reproductive mode
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.