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      Multiple components of feather microstructure contribute to structural plumage colour diversity in fairy-wrens

      1 , 2 , 2 , 1 , 1 , 3
      Biological Journal of the Linnean Society
      Oxford University Press (OUP)

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          Abstract

          Closely related species often differ in coloration. Understanding the mechanistic bases of such differences can reveal whether evolutionary changes in colour are driven by single key mechanisms or changes in multiple pathways. Non-iridescent structural plumage colours in birds are a good model in which to test these questions. These colours result from light absorption by pigments, light scattering by the medullary spongy layer (a nanostructure found within barbs) and contributions from other structural elements. Fairy-wrens (Malurus spp.) are a small clade of closely related birds that display a large diversity of ornamental structural colours. Using spectrometry, electron microscopy and Fourier analysis, we show that 30 structural colours, varying from ultraviolet to blue and purple, share a similar barb morphology. Despite this similarity, we find that at the microscopic scale, variation across multiple structural elements, including the size and density of the keratin cortex, spongy layer and melanin, explains colour diversity. These independent axes of morphological variation together account for sizeable amounts of structural colour variability (R2 = 0.21–0.65). The coexistence of many independent, evolutionarily labile mechanisms that generate colour variation suggests that the diversity of structural colours in this clade could be mediated by many independent genetic and environmental factors.

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          Most cited references43

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          Tetrachromacy, oil droplets and bird plumage colours

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            Theory of transparency of the eye.

            The present work relates the turbidity of the eye to microscopic spatial fluctuations in its index of refraction. Such fluctuations are indicated in electron microscope photographs. By examining the superposition of phases of waves scattered from each point in the medium, we provide a mathematical demonstration of the Bragg reflection principle which we have recently used in the interpretation of experimental investigations: namely, that the scattering of light is produced only by those fluctuations whose fourier components have a wavelength equal to or larger than one half the wavelength of light in the medium. This consideration is applied first to the scattering of light from collagen fibers in the normal cornea. We demonstrate physically and quantitatively that a limited correlation in the position of near neighbor collagen fibers leads to corneal transparency. Next, the theory is extended to predict the turbidity of swollen, pathologic corneas, wherein the normal distribution of collagen fibers is disturbed by the presence of numerous lakes-regions where collagen is absent. A quantitative expression for the turbidity of the swollen cornea is given in terms of the size and density of such lakes. Finally, the theory is applied to the case of the cataractous lens. We assume that the cataracts are produced by aggregation of the normal lens proteins into an albuminoid fraction and provide a formula for the lens turbidity in terms of the molecular weight and index of refraction of the individual albuminoid macromolecules. We provide a crude estimate of the mean albuminoid molecular weight required for lens opacity.
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              Coherent light scattering by blue feather barbs

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                Author and article information

                Journal
                Biological Journal of the Linnean Society
                Oxford University Press (OUP)
                0024-4066
                1095-8312
                November 2019
                October 18 2019
                September 04 2019
                November 2019
                October 18 2019
                September 04 2019
                : 128
                : 3
                : 550-568
                Affiliations
                [1 ]School of Biological Sciences, Monash University, Clayton, Victoria, Australia
                [2 ]Evolution and Optics of Nanostructures Group, Department of Biology, University of Ghent, Ghent, Belgium
                [3 ]Max Planck Institute for Ornithology, Vogelwarte Radolfzell, Radolfzell, Germany
                Article
                10.1093/biolinnean/blz114
                70ec7cd5-d433-4603-ae88-0198cf2f53fb
                © 2019

                https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model

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