» Articles » PMID: 18419340

Evolution of Avian Plumage Color in a Tetrahedral Color Space: a Phylogenetic Analysis of New World Buntings

Overview
Journal Am Nat
Specialties Biology
Science
Date 2008 Apr 19
PMID 18419340
Citations 107
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Hyperspectral imaging in animal coloration research: A user-friendly pipeline for image generation, analysis, and integration with 3D modeling.

Hogan B, Stoddard M PLoS Biol. 2024; 22(12):e3002867.

PMID: 39625994 PMC: 11614258. DOI: 10.1371/journal.pbio.3002867.


Size differences among canaries, goldfinches and allies may explain correlated evolution of song and colour.

Cardoso G, Abreu J, Mota P Proc Biol Sci. 2024; 291(2029):20241060.

PMID: 39196274 PMC: 11352604. DOI: 10.1098/rspb.2024.1060.


Ultraviolet vision in anemonefish improves colour discrimination.

Mitchell L, Phelan A, Cortesi F, Marshall N, Chung W, Osorio D J Exp Biol. 2024; 227(7).

PMID: 38586934 PMC: 11057877. DOI: 10.1242/jeb.247425.


A Breeding Plumage in the Making: The Unique Process of Plumage Coloration in the Crested Ibis in Terms of Chemical Composition and Sex Hormones.

Liu D, Tong Y, Dong R, Ye X, Yu X Animals (Basel). 2023; 13(24).

PMID: 38136856 PMC: 10740519. DOI: 10.3390/ani13243820.


Eggshell colour differences in a classic example of coevolved eggshell mimicry.

Villa J, Wisocki P, Dela Cruz J, Hanley D Biol Lett. 2023; 19(11):20230384.

PMID: 38016645 PMC: 10684340. DOI: 10.1098/rsbl.2023.0384.