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      3D Camouflage in an Ornithischian Dinosaur

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          Summary

          Countershading was one of the first proposed mechanisms of camouflage [ 1, 2]. A dark dorsum and light ventrum counteract the gradient created by illumination from above, obliterating cues to 3D shape [ 3, 4, 5, 6]. Because the optimal countershading varies strongly with light environment [ 7, 8, 9], pigmentation patterns give clues to an animal’s habitat. Indeed, comparative evidence from ungulates [ 9] shows that interspecific variation in countershading matches predictions: in open habitats, where direct overhead sunshine dominates, a sharp dark-light color transition high up the body is evident; in closed habitats (e.g., under forest canopy), diffuse illumination dominates and a smoother dorsoventral gradation is found. We can apply this approach to extinct animals in which the preservation of fossil melanin allows reconstruction of coloration [ 10, 11, 12, 13, 14, 15]. Here we present a study of an exceptionally well-preserved specimen of Psittacosaurus sp. from the Chinese Jehol biota [ 16, 17]. This Psittacosaurus was countershaded [ 16] with a light underbelly and tail, whereas the chest was more pigmented. Other patterns resemble disruptive camouflage, whereas the chin and jugal bosses on the face appear dark. We projected the color patterns onto an anatomically accurate life-size model in order to assess their function experimentally. The patterns are compared to the predicted optimal countershading from the measured radiance patterns generated on an identical uniform gray model in direct versus diffuse illumination. These studies suggest that Psittacosaurus sp. inhabited a closed habitat such as a forest with a relatively dense canopy.

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          Highlights

          • Preserved pigments in the dinosaur Psittacosaurus suggest countershading camouflage

          • We predicted the optimal countershading camouflage for different light environments

          • The dinosaur’s patterns would have been cryptic in a forest, but not open, habitat

          • We can also infer that dinosaur predators used shape-from-shading cues to detect prey

          Abstract

          Countershading camouflage uses a dark-to-light gradient from back to belly to counter the light-to-dark gradient created by illumination. The body appears flatter and less conspicuous. Vinther et al. use 3D reconstruction and radiance modeling to show that the dinosaur Psittacosaurus was countershaded and cryptic in a forested environment.

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          Most cited references49

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          An exceptionally preserved Lower Cretaceous ecosystem.

          Fieldwork in the Early Cretaceous Jehol Group, northeastern China has revealed a plethora of extraordinarily well-preserved fossils that are shaping some of the most contentious debates in palaeontology and evolutionary biology. These discoveries include feathered theropod dinosaurs and early birds, which provide additional, indisputable support for the dinosaurian ancestry of birds, and much new evidence on the evolution of feathers and flight. Specimens of putative basal angiosperms and primitive mammals are clarifying details of the early radiations of these major clades. Detailed soft-tissue preservation of the organisms from the Jehol Biota is providing palaeobiological insights that would not normally be accessible from the fossil record.
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            Disruptive coloration and background pattern matching.

            Effective camouflage renders a target indistinguishable from irrelevant background objects. Two interrelated but logically distinct mechanisms for this are background pattern matching (crypsis) and disruptive coloration: in the former, the animal's colours are a random sample of the background; in the latter, bold contrasting colours on the animal's periphery break up its outline. The latter has long been proposed as an explanation for some apparently conspicuous coloration in animals, and is standard textbook material. Surprisingly, only one quantitative test of the theory exists, and one experimental test of its effectiveness against non-human predators. Here we test two key predictions: that patterns on the body's outline should be particularly effective in promoting concealment and that highly contrasting colours should enhance this disruptive effect. Artificial moth-like targets were exposed to bird predation in the field, with the experimental colour patterns on the 'wings' and a dead mealworm as the edible 'body'. Survival analysis supported the predictions, indicating that disruptive coloration is an effective means of camouflage, above and beyond background pattern matching.
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              Plumage color patterns of an extinct dinosaur.

              For as long as dinosaurs have been known to exist, there has been speculation about their appearance. Fossil feathers can preserve the morphology of color-imparting melanosomes, which allow color patterns in feathered dinosaurs to be reconstructed. Here, we have mapped feather color patterns in a Late Jurassic basal paravian theropod dinosaur. Quantitative comparisons with melanosome shape and density in extant feathers indicate that the body was gray and dark and the face had rufous speckles. The crown was rufous, and the long limb feathers were white with distal black spangles. The evolution of melanin-based within-feather pigmentation patterns may coincide with that of elongate pennaceous feathers in the common ancestor of Maniraptora, before active powered flight. Feathers may thus have played a role in sexual selection or other communication.
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                Author and article information

                Contributors
                Journal
                Curr Biol
                Curr. Biol
                Current Biology
                Cell Press
                0960-9822
                1879-0445
                26 September 2016
                26 September 2016
                : 26
                : 18
                : 2456-2462
                Affiliations
                [1 ]School of Biological Sciences, University of Bristol, Life Sciences Building, 24 Tyndall Avenue, Bristol BS8 1TQ, UK
                [2 ]School of Earth Sciences, University of Bristol, Wills Memorial Building, Queens Road, Bristol BS8 1RJ, UK
                [3 ]Palaeocreations, 35 Hopps Road, Kingswood, Bristol BS15 9QQ, UK
                [4 ]Vertebrate Palaeontology Laboratory, Department of Earth Sciences, The University of Hong Kong, Pokfulam, Hong Kong
                [5 ]Burke Museum of Natural History and Culture, 4331 Memorial Way Northeast, Seattle, WA 98195, USA
                [6 ]Department of Ornithology, Senckenberg Research Institute and Natural History Museum, Senckenberganlage 25, 60325 Frankfurt, Germany
                Author notes
                []Corresponding author jakob.vinther@ 123456bristol.ac.uk
                [∗∗ ]Corresponding author i.cuthill@ 123456bristol.ac.uk
                [7]

                Lead Contact

                Article
                S0960-9822(16)30706-0
                10.1016/j.cub.2016.06.065
                5049543
                27641767
                a501ce52-fa54-446f-8ed2-471136812b5d
                © 2016 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 10 February 2016
                : 20 May 2016
                : 28 June 2016
                Categories
                Report

                Life sciences
                defensive coloration,countershading,paleocolor,jehol biota,yixian formation,paleoenvironment,behavioral ecology,taphonomy,soft-tissue preservation,lagerstätte

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