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40 results for “colour genetics”
The genetic basis of structural colour variation in mimetic Heliconius butterflies
<p>Raw USAXS data from discal region of <em>Heliconius </em>butterflies (<em>H. erato </em>and<em> H. melpomene</em>). The data comes from wings of individuals of two intercross families, one from each species and was used to estimate scale structure variation and a QTL analysis.</p>
Figure 2 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 2. - Neobythites bimarginatus. Pelvic-fin length and horizontal eye diameter showing negative allometric growth.
Figure 1 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 1. - Neobythites bimarginatus Fourmanoir & Rivaton, 1979. SAIAB 189024, SL 122 mm. From off Madagascar (photo M. Krag, ZMUC).
Fig. 2 in Genetically Determined Colour Polymorphism In Larvae Of Ceriagrion Chaoi (Insecta: Odonata: Coenagrionidae)
Fig. 2. Alignment of 454 bp partial sequences 16S rDNA of representative Ceriagrion chaoi and Ceriagrion cerinorubellum. CCHA1 = adult female of C. chaoi; CCHA2 = female exuvia of C. chaoi; CCHA4 = male brown larva of C. chaoi; CCHA6 = male black larva of C. chaoi; CCHA13 = dark larva* of C. chaoi; CCHA15 = brown larva* of C. chaoi; CCHA16 = brown larva of C. chaoi; CCER1 = C. cerinorubellum. *sex not determined.
The Camouflage Machine: Optimising protective colouration using deep learning with genetic algorithms
Evolutionary biologists frequently wish to measure the fitness of alternative phenotypes using behavioural experiments. However, many phenotypes are complex. For example colouration: camouflage aims to make detection harder, while conspicuous signals (e.g. for warning or mate attraction) require the opposite. Identifying the hardest and easiest to find patterns is essential for understanding the evolutionary forces that shape protective colouration, but the parameter space of potential patterns (coloured visual textures) is vast, limiting previous empirical studies to a narrow range of phenotypes. Here we demonstrate how deep learning combined with genetic algorithms can be used to augment behavioural experiments, identifying both the best camouflage and the most conspicuous signal(s) from an arbitrarily vast array of patterns. To show the generality of our approach, we do so for both trichromatic (e.g. human) and dichromat (e.g. typical mammalian) visual systems, in two different habitats. The patterns identified were validated using human participants; those identified as the best for camouflage were significantly harder to find than a tried-and-tested military design, while those identified as most conspicuous were significantly easier than other patterns. More generally, our method, dubbed the 'Camouflage Machine', will be a useful tool for identifying the optimal phenotype in high dimensional state-spaces.
Data from: Agonistic character displacement of genetically based male colour patterns across darters
Agonistic character displacement (ACD) occurs when selection to avoid maladaptive interspecific aggression leads to the evolution of agonistic signals and/or associated behavioural biases in sympatry. Here we test for a pattern consistent with ACD in male colour pattern in darters (Percidae: Etheostoma). Male colour pattern has been shown to function in male-male competition rather than female mating preferences in several darter species. Additionally, males bias their aggression towards conspecific over heterospecific males in sympatry but not in allopatry, consistent with divergent ACD in male behavioural biases. We use a common garden approach to show that differences in male colour pattern among four closely related darter species are genetically based. Additionally, we demonstrate that some aspects of male colour pattern exhibit enhanced differences in sympatric compared to allopatric populations of two darter species, consistent with ACD. However, other male colour traits are more similar between species in sympatry compared to allopatry, indicating that not all signal components are under strong divergent selection in sympatry. This study provides evidence that interspecific male-male aggressive interactions alone can promote elaborate male signal evolution both between and within species. We discuss the implications this has for male-driven ACD and cascade ACD.
Ecological, genetic and geographical divergence explain differences in sunbird (Nectariniidae) colouration
<p>Bird plumages are among the most elaborate ornaments, displaying almost all colours of the rainbow. Why and how birds are so colourful remains an open question with multiple and sometimes competing hypotheses. Different colours in different patches might have different functions and thus result from different forms of selection (e.g., natural vs. sexual selection). Here we test three hypotheses that might explain colour differences: (1) species isolation, (2) light environment, and (3) Brownian motion. We show that both natural and sexual selection affect the evolution of sunbird colouration, but that their extent and direction differs between sexes, by species interactions, and for different patches across the body. Even though overlap in the light environment explains part of colour differences in species, no colour metric (brightness and chroma) correlates to the light environment. It is likely that these results, where multiple forms of selection influence colouration in different ways, are more general across birds, highlighting the need to investigate bird colouration as a network of individual but inter-connected colour patches.</p>
Fig. 6 in Genetically Determined Colour Polymorphism In Larvae Of Ceriagrion Chaoi (Insecta: Odonata: Coenagrionidae)
Fig. 6. Ceriagrion chaoi male emerged from dark larva.
Fig. 5 in Genetically Determined Colour Polymorphism In Larvae Of Ceriagrion Chaoi (Insecta: Odonata: Coenagrionidae)
Fig. 5. Female Ceriagrion chaoi emerging from brown larva.
Fig. 1 in Genetically Determined Colour Polymorphism In Larvae Of Ceriagrion Chaoi (Insecta: Odonata: Coenagrionidae)
Fig. 1. Exuviae of brown (left) and dark (right) colour larvae of Ceriagrion chaoi.
The Camouflage Machine: Optimising protective colouration using deep learning with genetic algorithms
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Data from: Agonistic character displacement of genetically based male colour patterns across darters
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Data from: the quantitative genetic basis of variation in sexual versus non-sexual butterfly wing colouration: autosomal, Z-linked and maternal effects
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Ecological, genetic and geographical divergence explain differences in sunbird (Nectariniidae) colouration
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Data from: The many faced symbiotic snakelocks anemone (Anemonia viridis, Anthozoa): host and symbiont genetic differentiation among colour morphs
How can we explain morphological variations in a holobiont? The genetic determinism of phenotypes is not always obvious and could be circumstantial in complex organisms. In symbiotic cnidarians, it is known that morphology or colour can misrepresent a complex genetic and symbiotic diversity. Anemonia viridis is a symbiotic sea anemone from temperate seas. This species displays different colour morphs based on pigment content and lives in a wide geographical range. Here, we investigated whether colour morph differentiation correlated with host genetic diversity or associated symbiotic genetic diversity by using RAD-sequencing and symbiotic dinoflagellate typing of 140 sea anemones from the English Channel and the Mediterranean Sea. We did not observe genetic differentiation among colour morphs of A. viridis at the animal host or symbiont level, rejecting the hypothesis that A. viridis colour morphs correspond to species level differences. Interestingly, we however identified at least four independent animal host genetic lineages in A. viridis that differed in their associated symbiont populations. In conclusion, although the functional role of the different morphotypes of A. viridis remains to be determined, our approach provides new insights on the existence of cryptic species within A. viridis.
Data from: The colour of paternity: extra-pair paternity in the wild Gouldian finch does not appear to be driven by genetic incompatibility between morphs
In socially monogamous species, individuals can use extra-pair paternity and offspring sex allocation as adaptive strategies to ameliorate costs of genetic incompatibility with their partner. Previous studies on domesticated Gouldian finches (Erythrura gouldiae) demonstrated a genetic incompatibility between head colour morphs, the effects of which are more severe in female offspring. Domesticated females use differential sex allocation, and extra-pair paternity with males of compatible head colour, to reduce fitness costs associated with incompatibility in mixed-morph pairings. However, laboratory studies are an oversimplification of the complex ecological factors experienced in the wild, and may only reflect the biology of a domesticated species. This study aimed to examine the patterns of parentage and sex-ratio bias with respect to colour pairing combinations in a wild population of the Gouldian finch. We utilized a novel PCR assay that allowed us to genotype the morph of offspring before the morph phenotype develops, and to explore bias in morph paternity and selection at the nest. Contrary to previous findings in the laboratory, we found no effect of pairing combinations on patterns of extra-pair paternity, offspring sex ratio, or selection on morphs in nestlings. In the wild, the effect of morph incompatibility is likely much smaller, or absent, than was observed in the domesticated birds. Furthermore, the previously studied domesticated population is genetically differentiated from the wild population, consistent with the effects of domestication. It is possible that the domestication process fostered the emergence (or enhancement) of incompatibility between colour morphs previously demonstrated in the laboratory.
Data from: Genetics and evidence for balancing selection of a sex-linked colour polymorphism in a songbird
Colour polymorphisms play a key role in sexual selection and speciation, yet the mechanisms that generate and maintain them are not fully understood. Here, we use genomic and transcriptomic tools to identify the precise genetic architecture and evolutionary history of a sex-linked colour polymorphism in the Gouldian finch Erythrura gouldiae that is also accompanied by remarkable differences in behaviour and physiology. We find that differences in colour are associated with an ~72-kbp region of the Z chromosome in a putative regulatory region for follistatin, an antagonist of the TGF-β superfamily genes. The region is highly differentiated between morphs, unlike the rest of the genome, yet we find no evidence that an inversion is involved in maintaining the distinct haplotypes. Coalescent simulations confirm that there is elevated nucleotide diversity and an excess of intermediate frequency alleles at this locus. We conclude that this pleiotropic colour polymorphism is most probably maintained by balancing selection.
Data from: Colour in a new light: a spectral perspective on the quantitative genetics of carotenoid coloration
1. Carotenoid-based colours are model traits for research on animal signalling and sexual selection but, whereas the consequences of variable expression have been extensively studied, its causes are rarely quantified. This issue is complicated by the composite nature of carotenoid-based colour patches, which combine pigments and a reflective background. Ultimately, the evolution of such colours will be determined by the processes that govern variable expression of these mechanisms. 2. We present a novel approach to assessing the quantitative genetics of colour expression, in which reflectance spectra are analysed directly, thereby avoiding the data loss and inherent subjectivity of summary colour variables. Further, the influence of the multiple component mechanisms can be distinguished in spectral analyses due to their contrasting wavelength-dependencies. 3. Using data from a six-year study of carotenoid-based plumage reflectance in wild great tits (Parus major), we employ a multi-parallel 'animal modelling' approach to estimate sources of variance for narrow (2nm) wavebands across the visible spectrum. 4. Moderate heritability estimates were limited to the violet-blue region of the spectrum, diagnostic of the carotenoid content of plumage being heritable. The natal environment effect was limited entirely to the violet-blue, again indicating that it relates to variation in carotenoid content of feathers. Other wavelengths were sensitive to annual and permanent environmental variation but only marginally influenced by additive genetic variation. Hence background reflectance is the component that is more sensitive to the environment. 5. Analysing reflectance spectra directly provided an objective perspective of the dynamics of colour expression that is not apparent when relying on summary colour scores. In this case, our results suggest that carotenoid deposition may be an effective target of selection and hence could explain the important role carotenoids frequently play in intraspecific signalling.
Quantitative genetics of eggshell colouration
<p>Exploring the evolutionary architecture of female sexual traits and their potential evolvability is important to understand their possible role as post-mating sexual signals. Egg colouration has been proposed to be one of these post-mating sexual signals, honestly advertising female quality in birds, especially in blue-green laying species. In this study, we used an animal model in a Bayesian framework to estimate the evolvability of multiple descriptors of blue-green egg colouration and egg size in a wild long-term monitored population of spotless starlings (<em>Sturnus unicolor</em>). Our results show low to moderate heritability (<em>h</em><sup>2 </sup>= 0.31 – 0.44) for three egg colour descriptors (blue-green chroma, chroma and lightness) and egg size. Using the coefficient of additive genetic variance (<em>CV</em><sub>A</sub>) and the evolvability (<em>I</em><sub>A</sub>) as proxies of evolutionary potential of all components of this trait, we found low values of <em>C</em><em>V</em><sub>A</sub> for all these variables, suggesting a small evolutionary potential of these phenotypic traits, contrasting to previous results reported in another blue-green egg laying species. Our results indicate a modest raw genetic material of this trait on which sexual selection can act upon and, therefore, a small probability for these traits to respond easily to selection.</p>
Data from: Colour ornamentation in the blue tit: quantitative genetic (co)variances across sexes
Although secondary sexual traits are commonly more developed in males than females, in many animal species females also display elaborate ornaments or weaponry. Indirect selection on correlated traits in males and/or direct sexual or social selection in females are hypothesized to drive the evolution and maintenance of female ornaments. Yet, the relative roles of these evolutionary processes remain unidentified, because little is known about the genetic correlation that might exist between the ornaments of both sexes, and few estimates of sex-specific autosomal or sex-linked genetic variances are available. In this study, we used two wild blue tit populations with 9 years of measurements on two colour ornaments: one structurally based (blue crown) and one carotenoid based (yellow chest). We found significant autosomal heritability for the chromatic part of the structurally based colouration in both sexes, whereas carotenoid chroma was heritable only in males, and the achromatic part of both colour patches was mostly non heritable. Power limitations, which are probably common among most data sets collected so far in wild populations, prevented estimation of sex-linked genetic variance. Bivariate analyses revealed very strong cross-sex genetic correlations in all heritable traits, although the strength of these correlations was not related to the level of sexual dimorphism. In total, our results suggest that males and females share a majority of their genetic variation underlying colour ornamentation, and hence the evolution of these sex-specific traits may depend greatly on correlated responses to selection in the opposite sex.
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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.