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399 results for “mimicry”
Fig. 2. Heterotypic schooling involving the genus Haemulon and other coral reef fish species. A in Mixed-species schooling behavior and protective mimicry involving coral reef fish from the genus Haemulon (Haemulidae)
Fig. 2. Heterotypic schooling involving the genus Haemulon and other coral reef fish species. A) Anisotremus virginicus with school of adult H. aurolineatum; B) Ocyurus chrysurus with adult H. aurolineatum and H. squamipinna; C) Scarus zelindae with adult H. parra, H. plumieri and H. squamipinna; D) Lutjanus jocu with adult H. parra and H. squamipinna. Circles highlight the non-Haemulon species. Photos: P. H. C. Pereira
Fig. 3. Protective mimicry between select reef fish species and the genus Haemulon. A in Mixed-species schooling behavior and protective mimicry involving coral reef fish from the genus Haemulon (Haemulidae)
Fig. 3. Protective mimicry between select reef fish species and the genus Haemulon. A) Mulloidichthys martinicus with a school of adult H. aurolineatum; B) Sparisoma axillare with H. parra juveniles; C) Harengula clupeola with a school of juvenile H. aurolineatum. Circles highlight non-Haemulon species. Photos: P. H. C. Pereira
Hard to catch: experimental evidence supports evasive mimicry
<p></p><p>Most research on aposematism has focused on chemically defended prey, but the signaling difficulty of capture remains poorly explored. Similar to classical Batesian and Müllerian mimicry related to distastefulness, such 'evasive aposematism' may also lead to convergence in warning colours, known as evasive mimicry. A prime candidate group for evasive mimicry areAdelphabutterflies, which are agile insects and show remarkable colour pattern convergence. We tested the ability of naive blue tits to learn to avoid and generalizeAdelphawing patterns associated with the difficulty of capture and compared their response to that of birds that learned to associate the same wing patterns with distastefulness. Birds learned to avoid all wing patterns tested and generalized their aversion to other prey to some extent, but learning was faster with evasive prey compared to distasteful prey. Our results on generalization agree with longstanding observations of striking convergence in wing colour patterns amongAdelphaspecies, since, in our experiments, perfect mimics of evasive and distasteful models were always protected during generalization and suffered the lowest attack rate. Moreover, generalization on evasive prey was broader compared to that on distasteful prey. Our results suggest that being hard to catch may deter predators at least as effectively as distastefulness. This study provides empirical evidence for evasive mimicry, a potentially widespread but poorly understood form of morphological convergence driven by predator selection.</p><p></p>
Combined measures of mimetic fidelity explain imperfect mimicry in a brood parasite–host system
<p>The persistence of imperfect mimicry in nature presents a challenge to mimicry theory. Some hypotheses for the existence of imperfect mimicry make differing predictions depending on how mimetic fidelity is measured. Here, we measure mimetic fidelity in a brood parasite–host system using both trait-based and response-based measures of mimetic fidelity. Cuckoo finches <em>Anomalospiza</em> <em>imberbis</em> lay imperfectly mimetic eggs that lack the fine scribbling characteristic of eggs of the tawny-flanked prinia <em>Prinia</em> <em>subflava</em>, a common host species. A trait-based discriminant analysis based on Minkowski functionals—that use geometric and topological morphometric methods related to egg pattern shape and coverage—reflects this consistent difference between host and parasite eggs. These methods could be applied to quantify other phenotypes including stripes and waved patterns. Furthermore, by painting scribbles onto cuckoo finch eggs and testing their rate of rejection compared to control eggs (i.e. a response-based approach to quantify mimetic fidelity), we show that prinias do not discriminate between eggs based on the absence of scribbles. Overall, our results support relaxed selection on cuckoo finches to mimic scribbles, since prinias do not respond differently to eggs with and without scribbles, despite the existence of this consistent trait difference.</p>
Data for: Aggressive hosts are undeterred by a cuckoo's hawk mimicry, but probably make good foster parents
<p>Parasites face a trade-off if the highest quality hosts are also most resistant to exploitation. For brood parasites, well-defended host nests may be both harder to parasitize and harder to predate, leading to better survival of parasitic chicks. This trade-off could be accentuated if brood-parasitic adaptations to reduce front-line defences of hosts, such as mimicry of hawks by Cuculus cuckoos, do not deter hosts which aggressively mob raptors. Here we investigate the costs and benefits to the African cuckoo (Cuculus gularis) of specializing on a highly aggressive host species, the fork-tailed drongo (Dicrurus adsimilis). Field experiments showed that drongos strongly attacked and mobbed both cuckoo and hawk models, implying that hawk mimicry does not deter front-line defences against African cuckoos. Attacks on cuckoo and hawk models generally declined after the egg stage but attacks on snake models sharply increased, suggesting drongos may treat hawks more like cuckoos than predators. We suggest that the cost to cuckoos of parasitizing an aggressive host may be alleviated by subsequent benefits to their offspring, since drongo nests survived better than nests of other species with similar nesting ecology. These results are indicative of a trade-off between host quality and susceptibility for a brood parasite.</p>
Combined measures of mimetic fidelity explain imperfect mimicry in a brood parasite–host system
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Phylogeny, systematics and evolution of mimicry patterns in Neotropical limenitidine butterflies
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Data from: Behavioural mimicry among poison frogs diverges during close-range encounters with predators
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Data from: Is temporal synchrony necessary for effective Batesian mimicry?
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Uncovering the effects of Müllerian mimicry on the evolution of conspicuousness in colour patterns
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Data for: Aggressive hosts are undeterred by a cuckoo's hawk mimicry, but probably make good foster parents
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Eggshell colour differences in a classic example of coevolved eggshell mimicry
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Predator-based selection and the impact of edge sympatry on components of coral snake mimicry
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Chase-away evolution maintains imperfect mimicry despite rapid evolution of mimics
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Selection for evasive mimicry imposed by an arthropod predator
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Functional genetic elements of a butterfly mimicry supergene
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Hard to catch: experimental evidence supports evasive mimicry
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Data from: Being a bright snake: testing aposematism and mimicry in a Neotropical forest
Based on color patterns and behavioral similarities, venomous coral snake Micrurus corallinus (Elapidae) may act as a model for two polymorphic species, Erythrolamprus aesculapii (Dipsadidae) and Micrurus decoratus (Elapidae). Plasticine replicas were used to investigate the aposematism of these coloration patterns and whether these species may be part of mimetic complexes in two Atlantic Forest localities in South-east Brazil. Coral replicas were more avoided when set upon a white background, evincing that the pattern may act aposematically in contrast with light substrates. Birds attacked all four patterns equally during the mimicry experiments. Birds of prey, known to be effective in predating snakes, are quite abundant in the study areas, which may have led to this lack of avoidance. Accordingly, they predated more adult-sized replicas, which could be more dangerous. Interestingly, opossum avoided the Micrurus corallinus and Erythrolamprus aesculapii replicas that resembled the model. This suggests that opportunistic predators, as the opossum may be important selective agents in mimicry complexes.
Data from: A multilocus analysis of Epicopeiidae (Lepidoptera, Geometroidea) provides new insights into their relationships and the evolutionary history of mimicry
<p>The family Epicopeiidae is a small group of day-flying moths, known for mimicking many different groups of butterflies and moths. So far, there still lacks a reliable phylogenetic framework of Epicopeiidae that is necessary to our understanding of the evolutionary process of their mimicry. In this study, we sequenced 94 nuclear protein-coding markers for 56 epicopeiid samples and 11 outgroups, covering all ten genera of Epicopeiidae. We used homemade PCR-generated baits to capture target sequences, which allowed us to utilize old and dried specimens that were difficult to handle by conventional PCR + Sanger sequencing. Maximum likelihood and Bayesian analyses of the newly obtained dataset (86,388 bp) at both DNA and protein levels produced identical phylogenies with strong support. The non-mimicry genus <em>Deuveia</em> is the sister group of other epicopeiid genera. <em>Epicopeia</em> and <em>Nossa</em> are not monophyletic, and these two genera nest together to form a clade. We also estimated divergence times of Epicopeiidae and found that their initial diversification happened in Eocene about 41 million years ago. The ancestral state reconstruction of mimicry type for this family suggested that the last common ancestor of epicopeiid moths is non-mimetic, and the Riodinidae-mimicry type evolved first. In summary, our work provides a comprehensive and robust time-calibrated phylogeny of Epicopeiidae that provides a sound framework for revising their classification and interpreting character evolution.</p>
Data from: Multimodal mimicry of hosts in a radiation of parasitic finches
<p>Brood parasites use the parental care of others to raise their young and sometimes employ mimicry to dupe their hosts. The brood-parasitic finches of the genus <i>Vidua</i> are a textbook example of the role of imprinting in sympatric speciation. Sympatric speciation is thought to occur in <i>Vidua</i> because their mating traits and host preferences are strongly influenced by their early host environment. However, this alone may not be sufficient to isolate parasite lineages, and divergent ecological adaptations may also be required to prevent hybridisation collapsing incipient species. Using pattern recognition software and classification models, we provide quantitative evidence that <i>Vidua</i> exhibit specialist mimicry of their grassfinch hosts, matching the patterns, colours and sounds of their respective host's nestlings. We also provide qualitative evidence of mimicry in postural components of <i>Vidua</i> begging. Quantitative comparisons reveal small discrepancies between parasite and host phenotypes, with parasites sometimes exaggerating their host's traits. Our results support the hypothesis that behavioural imprinting on hosts has not only enabled the origin of new <i>Vidua</i> species, but also set the stage for the evolution of host-specific, ecological adaptations.</p>
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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)
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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.