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37 results for “colour signal”
Data from: Colour change on different body regions provides thermal and signalling advantages in bearded dragon lizards
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Data from: Losing the trait without losing the signal: evolutionary shifts in communicative colour signalling
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Data from: Prey with hidden colour defences benefit from their similarity to aposematic signals
<p>Some camouflaged animals hide colour signals and display them only transiently. These hidden colour signals are often conspicuous and are used as a secondary defence to warn or startle predators (deimatic displays) and/or to confuse them (flash displays). The hidden signals used in these displays frequently resemble typical aposematic signals, so it is possible that prey with hidden signals have evolved to employ colour patterns of a form that predators have previously learned to associate with unprofitability. Here, we tested this hypothesis by conducting two experiments that examined the effect of predator avoidance learning on the efficacy of deimatic and flash displays. We found that the survival benefits of both deimatic and flash displays were substantially higher against educated predators than naïve ones. These findings help explain the phenological patterns we found in 1,568 macro-lepidopteran species on three continents: species with hidden signals tend to occur later in the season than species without hidden signals.</p>
Data from: Do trace metals influence visual signals? Effects of trace metals on iridescent and melanic feather colouration in the feral pigeon
Trace metals are chemical pollutants of prime concern nowadays given their implication in several human diseases and their noxious effects on wildlife. Previous studies demonstrated their negative (e.g. lead, cadmium) or positive (e.g. zinc) effects on body condition, immunity and reproductive success in birds. Because of their effects on bird condition, trace metals are likely to influence the production of condition-dependent plumage colours, that may be used in mate choice. In the feral pigeon Columba livia, we investigated iridescent colouration in response to lead and zinc experimental (i.e. metal supplementation in standardized conditions) and natural exposure (i.e. metal concentrations in feathers of wild urban pigeons), and melanic feather colouration in response to experimental lead and zinc exposure. Both studies (i.e. experimental and correlative) consistently showed that lead exposure decreased iridescent neck feather brightness independently of colour morph. Moreover, lead, when provided alone, decreased melanic feather reflectance in the middle wavelengths while zinc supplementation increased melanic feather reflectance in the violet-wavelength. In conclusion, our study suggests that the colouration of iridescent and melanic feathers depends on the exposure to pollutants. Whether trace metal exposure affected the ability of birds to produce melanin pigments, to grow the microstructural feather elements required for maximum colour display, or to cope with bacteria that degrade feather microstuctures remains unclear. Future studies should investigate whether these metal-induced modifications of plumage colouration affect behaviours involved in sexual selection.
Data from: Experimental evidence that primate trichromacy is well suited for detecting primate social colour signals
Primate trichromatic colour vision has been hypothesized to be well tuned for detecting variation in facial coloration, which could be due to selection on either signal wavelengths or the sensitivities of the photoreceptors themselves. We provide one of the first empirical tests of this idea by asking whether, when compared with other visual systems, the information obtained through primate trichromatic vision confers an improved ability to detect the changes in facial colour that female macaque monkeys exhibit when they are proceptive. We presented pairs of digital images of faces of the same monkey to human observers and asked them to select the proceptive face. We tested images that simulated what would be seen by common catarrhine trichromatic vision, two additional trichromatic conditions and three dichromatic conditions. Performance under conditions of common catarrhine trichromacy, and trichromacy with narrowly separated LM cone pigments (common in female platyrrhines), was better than for evenly spaced trichromacy or for any of the dichromatic conditions. These results suggest that primate trichromatic colour vision confers excellent ability to detect meaningful variation in primate face colour. This is consistent with the hypothesis that social information detection has acted on either primate signal spectral reflectance or photoreceptor spectral tuning, or both.
Data from: Body size affects the evolution of hidden colour signals in moths
Many cryptic prey have also evolved hidden contrasting colour signals which are displayed to would-be predators. Given that these hidden contrasting signals may confer additional survival benefits to the prey by startling/intimidating predators, it is unclear why they have evolved in some species, but not in others. Here, we have conducted a comparative phylogenetic analysis of the evolution of colour traits in the family Erebidae (Lepidoptera), and found that the hidden contrasting colour signals are more likely to be found in larger species. To understand why this relationship occurs, we present a general mathematical model, demonstrating that selection for a secondary defence such as deimatic display will be stronger in large species when (i) the primary defence (crypsis) is likely to fail as its body size increases and/or (ii) the secondary defence is more effective in large prey. To test the model assumptions, we conducted behavioural experiments using a robotic moth which revealed that survivorship advantages were higher against wild birds when the moth has contrasting hindwings and large size. Collectively, our results suggest that the evolutionary association between large size and hidden contrasting signals has been driven by a combination of the need for a back-up defence and its efficacy.
Data from: Categorical colour perception occurs in both signalling and non-signalling colour ranges in a songbird
Although perception begins when a stimulus is transduced by a sensory neuron, numerous perceptual mechanisms can modify sensory information as it is processed by an animal's nervous system. One such mechanism is categorical perception, in which 1) continuously-varying stimuli are labelled as belonging to a discrete number of categories and 2) there is enhanced discrimination between stimuli from different categories as compared to equally-different stimuli from within the same category. We have shown previously that female zebra finches (Taeniopygia guttata) categorically perceive colours along an orange-red continuum that aligns with the carotenoid-based colouration of male beaks, a trait that serves as an assessment signal in female mate choice. Here we demonstrate that categorical perception occurs along a blue-green continuum as well, suggesting that categorical colour perception may be a general feature of zebra finch vision. Although we identified two categories in both the blue-green and the orange-red ranges, we also found that individuals could better differentiate colours from within the same category in the blue-green as compared to the orange-red range, indicative of less clear categorization in the blue-green range. We discuss reasons why categorical perception may vary across the visible spectrum, including the possibility that such differences are linked to the behavioural or ecological function of different colour ranges.
Data from: Conflict between background matching and social signalling in a colour-changing freshwater fish
The ability to change coloration allows animals to modify their patterning to suit a specific function. Many freshwater fishes, for example, can appear cryptic by altering the dispersion of melanin pigment in the skin to match the visual background. However, melanin-based pigments are also used to signal dominance among competing males; thus colour change for background matching may conflict with colour change for social status signalling. We used a colour-changing freshwater fish to investigate whether colour change for background matching influenced aggressive interactions between rival males. Subordinate males that had recently darkened their skin for background matching received heightened aggression from dominant males, relative to males whose coloration had not changed. We then determined whether the social status of a rival male, the focal male's previous social status, and his previous skin coloration, affected a male's ability to change colour for background matching. Social status influenced skin darkening in the first social encounter, with dominant males darkening more than subordinate males, but there was no effect of social status on colour change in the second social encounter. We also found that the extent of skin colour change (by both dominant and subordinate males) was dependent on previous skin coloration, with dark males displaying a smaller change in coloration than pale males. Our findings suggest that skin darkening for background matching imposes a significant social cost on subordinate males in terms of increased aggression. We also suggest that the use of melanin-based signals during social encounters can impede subsequent changes in skin coloration for other functions, such as skin darkening for background matching.
Data from: Conflict between background matching and social signalling in a colour-changing freshwater fish
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Data from: Categorical colour perception occurs in both signalling and non-signalling colour ranges in a songbird
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Data from: Experimental evidence that primate trichromacy is well suited for detecting primate social colour signals
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Data from: Body size affects the evolution of hidden colour signals in moths
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Data from: Candidate genes for colour and vision exhibit signals of selection across the pied flycatcher (Ficedula hypoleuca) breeding range
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Data from: Does plumage colour signal fitness in the tawny owl Strix aluco?
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Data from: Do trace metals influence visual signals? Effects of trace metals on iridescent and melanic feather colouration in the feral pigeon
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Data from: Prey with hidden colour defences benefit from their similarity to aposematic signals
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Figure 1 in Phylogenetic signal in the evolution of body colour and spicule skeleton in calcareous sponges
Figure 1. Maximum-likelihood (ML) tree based on a concatenated sequence of ITS1, 5.8S, ITS2 and the D2 region of 28S using the GTR model with six gamma categories. Bootstrap values for ML and maximum-parsimony (MP), respectively, are given on interior branches. An asterisk indicates ML interior branches that were not present on the MP topology. Thick branches specify those on which listed character changes were inferred.
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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.