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      The dynamics of color signals in male threespine sticklebacks Gasterosteus aculeatus

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          Abstract

          Body coloration and color patterns are ubiquitous throughout the animal kingdom and vary between and within species. Recent studies have dealt with individual dynamics of various aspects of coloration, as it is in many cases a flexible trait and changes in color expression may be context-dependent. During the reproductive phase, temporal changes of coloration in the visible spectral range (400–700 nm) have been shown for many animals but corresponding changes in the ultraviolet (UV) waveband (300–400 nm) have rarely been studied. Threespine stickleback Gasterosteus aculeatus males develop conspicuous orange–red breeding coloration combined with UV reflectance in the cheek region. We investigated dynamics of color patterns including UV throughout a male breeding cycle, as well as short-term changes in coloration in response to a computer-animated rival using reflectance spectrophotometry and visual modeling, to estimate how colors would be perceived by conspecifics. We found the orange–red component of coloration to vary during the breeding cycle with respect to hue ( theta/R50) and intensity (achieved chroma/red chroma). Furthermore, color intensity in the orange–red spectral part (achieved chroma) tended to be increased after the presentation of an artificial rival. Dynamic changes in specific measures of hue and intensity in the UV waveband were not found. In general, the orange–red component of the signal seems to be dynamic with respect to color intensity and hue. This accounts in particular for color changes during the breeding cycle, presumably to signal reproductive status, and with limitations as well in the intrasexual context, most likely to signal dominance or inferiority.

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          Exploitation of Sexual Signals by Predators and Parasitoids

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            Female sticklebacks use male coloration in mate choice and hence avoid parasitized males

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              Evolution of avian plumage color in a tetrahedral color space: a phylogenetic analysis of new world buntings.

              We use a tetrahedral color space to describe and analyze male plumage color variation and evolution in a clade of New World buntings--Cyanocompsa and Passerina (Aves: Cardinalidae). The Goldsmith color space models the relative stimulation of the four retinal cones, using the integrals of the product of plumage reflectance spectra and cone sensitivity functions. A color is represented as a vector defined by the relative stimulation of the four cone types--ultraviolet, blue, green, and red. Color vectors are plotted in a tetrahedral, or quaternary, plot with the achromatic point at the origin and the ultraviolet/violet channel along the Z-axis. Each color vector is specified by the spherical coordinates theta, phi, and r. Hue is given by the angles theta and phi. Chroma is given by the magnitude of r, the distance from the achromatic origin. Color vectors of all distinct patches in a plumage characterize the plumage color phenotype. We describe the variation in color space occupancy of male bunting plumages, using various measures of color contrast, hue contrast and diversity, and chroma. Comparative phylogenetic analyses using linear parsimony (in MacClade) and generalized least squares (GLS) models (in CONTINUOUS) with a molecular phylogeny of the group document that plumage color evolution in the clade has been very dynamic. The single best-fit GLS evolutionary model of plumage color variation over the entire clade is a directional change model with no phylogenetic correlation among species. However, phylogenetic innovations in feather color production mechanisms--derived pheomelanin and carotenoid expression in two lineages--created new opportunities to colonize novel areas of color space and fostered the explosive differentiation in plumage color. Comparison of the tetrahedral color space of Goldsmith with that of Endler and Mielke demonstrates that both provide essentially identical results. Evolution of avian ultraviolet/violet opsin sensitivity in relation to chromatic experience is discussed.
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                Author and article information

                Journal
                Curr Zool
                Curr Zool
                czoolo
                czoolo
                Current Zoology
                Oxford University Press
                1674-5507
                February 2016
                10 February 2016
                10 February 2016
                : 62
                : 1
                : 23-31
                Affiliations
                aInstitute for Evolutionary Biology and Ecology, University of Bonn, An der Immenburg 1, 53121 Bonn, Germany
                Author notes
                *Address correspondence to Meike Hiermes. E-mail: mhiermes@ 123456evolution.uni-bonn.de .
                Article
                zov009
                10.1093/cz/zov009
                5804133
                29491887
                eac0af60-a34f-49d3-abe9-3741f896db76
                © The Author (2016). Published by Oxford University Press.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 14 January 2015
                : 16 April 2015
                Page count
                Pages: 9
                Categories
                Articles

                breeding season,color change,color signals,stickleback,structural coloration,uv coloration

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