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MEET the BUTTERFLIES Identify the Butter Ies You've Seen at Butter Ies
MEET THE BUTTERFLIES Identify the butteries you’ve seen at Butteries LIVE! Learn the scientic, common name and country of origin. Experience the wonderful world of butteries with the help of Butteries LIVE! COMMON MORPHO Morpho peleides Family: Nymphalidae Range: Mexico to Colombia Wingspan: 5-8 in. (12.7 – 20.3 cm.) Fast Fact: Common morphos are attracted to fermenting fruits. WHITE MORPHO Morpho polyphemus Family: Nymphalidae Range: Mexico to Central America Wingspan: 4-4.75 in. (10-12 cm.) Fast Fact: Adult white morphos prefer to feed on rotting fruits or sap from trees. WHITENED BLUEWING Myscelia cyaniris Family: Nymphalidae Range: Mexico, parts of Central and South America Wingspan: 1.3-1.4 in. (3.3-3.6 cm.) Fast Fact: The underside of the whitened bluewing is silvery- gray, allowing it to blend in on bark and branches. MEXICAN BLUEWING Myscelia ethusa Family: Nymphalidae Range: Mexico, Central America, Colombia Wingspan: 2.5-3.0 in. (6.4-7.6 cm.) Fast Fact: Young caterpillars attach dung pellets and silk to a leaf vein to create a resting perch. NEW GUINEA BIRDWING Ornithoptera priamus Family: Papilionidae Range: Australia Wingspan: 5 in. (12.7 cm.) Fast Fact: New Guinea birdwings are sexually dimorphic. Females are much larger than the males, and their wings are black with white markings. LEARN MORE ABOUT SEXUAL DIMORPHISM IN BUTTERFLIES > MOCKER SWALLOWTAIL Papilio dardanus Family: Papilionidae Range: Africa Wingspan: 3.9-4.7 in. (10-12 cm.) Fast Fact: The male mocker swallowtail has a tail, while the female is tailless. LEARN MORE ABOUT SEXUALLY DIMORPHIC BUTTERFLIES > ORCHARD SWALLOWTAIL Papilio demodocus Family: Papilionidae Range: Africa and Arabia Wingspan: 4.5 in. -
A Comprehensive Multilocus Phylogeny of the Neotropical Cotingas
Molecular Phylogenetics and Evolution 81 (2014) 120–136 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A comprehensive multilocus phylogeny of the Neotropical cotingas (Cotingidae, Aves) with a comparative evolutionary analysis of breeding system and plumage dimorphism and a revised phylogenetic classification ⇑ Jacob S. Berv 1, Richard O. Prum Department of Ecology and Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208105, New Haven, CT 06520, USA article info abstract Article history: The Neotropical cotingas (Cotingidae: Aves) are a group of passerine birds that are characterized by Received 18 April 2014 extreme diversity in morphology, ecology, breeding system, and behavior. Here, we present a compre- Revised 24 July 2014 hensive phylogeny of the Neotropical cotingas based on six nuclear and mitochondrial loci (7500 bp) Accepted 6 September 2014 for a sample of 61 cotinga species in all 25 genera, and 22 species of suboscine outgroups. Our taxon sam- Available online 16 September 2014 ple more than doubles the number of cotinga species studied in previous analyses, and allows us to test the monophyly of the cotingas as well as their intrageneric relationships with high resolution. We ana- Keywords: lyze our genetic data using a Bayesian species tree method, and concatenated Bayesian and maximum Phylogenetics likelihood methods, and present a highly supported phylogenetic hypothesis. We confirm the monophyly Bayesian inference Species-tree of the cotingas, and present the first phylogenetic evidence for the relationships of Phibalura flavirostris as Sexual selection the sister group to Ampelion and Doliornis, and the paraphyly of Lipaugus with respect to Tijuca. -
Morpho 1.11.0 User Guide
MORPHO 1.11.0 USER GUIDE APRIL 2015 NATIONAL CENTER FOR ECOLOGICAL ANALYSIS AND SYNTHESIS KNOWLEDGE NETWORK FOR BIOCOMPLEXITY Contents 1 Introduction2 1.1 What is Morpho?.........................2 1.2 Terms you need to know.....................2 1.2.1 Metadata.........................3 1.2.2 Data Package.......................3 2 Getting Started4 2.1 System Requirements......................4 2.2 Downloading and Installing Morpho...............4 2.3 Before you Begin.........................5 2.3.1 Register for the KNB Network..............5 2.3.2 Create a User Profile...................5 2.4 Logging In.............................8 2.5 Removing a profile........................9 3 The Morpho Interface: The Main Screen 11 3.1 Panels............................... 11 3.1.1 Current profile...................... 11 3.1.2 Network Status...................... 12 3.1.3 Work with your data. .................. 13 3.2 Menu bar............................. 13 3.2.1 File menu......................... 13 3.2.2 Edit menu......................... 13 3.2.3 Search menu....................... 15 3.2.4 Documentation menu.................. 15 3.2.5 Data menu........................ 15 3.2.6 Window menu...................... 17 3.2.7 Help menu........................ 17 3.3 Toolbar.............................. 17 3.4 Status Bar............................. 18 4 Opening and Viewing a Data Package 20 4.1 Opening Data Packages..................... 20 4.1.1 Opening a Shared Data Package............ 22 4.1.2 Opening a Data Package by Package Id........ 22 4.2 Viewing a Data Package: The Data Package Interface.... 23 4.2.1 Package Documentation panel............. 23 4.2.2 Data Table panel..................... 24 4.2.3 Table Documentation panel............... 25 5 Searching for Data Packages 28 5.1 Opening the Search Interface and Performing a Search.. -
Another Darwinian Aesthetics
This is a repository copy of Another Darwinian Aesthetics. White Rose Research Online URL for this paper: https://eprints.whiterose.ac.uk/103826/ Version: Accepted Version Article: Wilson, Catherine orcid.org/0000-0002-0760-4072 (2016) Another Darwinian Aesthetics. Journal of aesthetics and art criticism. pp. 237-252. ISSN 0021-8529 https://doi.org/10.1111/jaac.12283 Reuse Items deposited in White Rose Research Online are protected by copyright, with all rights reserved unless indicated otherwise. They may be downloaded and/or printed for private study, or other acts as permitted by national copyright laws. The publisher or other rights holders may allow further reproduction and re-use of the full text version. This is indicated by the licence information on the White Rose Research Online record for the item. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. [email protected] https://eprints.whiterose.ac.uk/ Another Darwinian Aesthetics (Last ms version). Published Version: WILSON, CATHERINE. "Another Darwinian Aesthetics." The Journal of Aesthetics and Art Criticism 74.3 (2016): 237-252. Despite the bright sun, dew was still dripping from the chrysanthemums in the garden. On the bamboo fences, and criss-cross hedges, I saw tatters of spiderwebs; and where the threads were broken the raindrops hung on them like strings of white pearls. I was greatly moved and delighted. …Later I described to people how beautiful it all was. -
Current Perspectives on Sexual Selection History, Philosophy and Theory of the Life Sciences Volume 9
Current Perspectives on Sexual Selection History, Philosophy and Theory of the Life Sciences Volume 9 Editors: Charles T. Wolfe, Ghent University, Belgium Philippe Huneman, IHPST (CNRS/Université Paris I Panthéon-Sorbonne), France Thomas A.C. Reydon, Leibniz Universität Hannover, Germany Editorial Board: Editors Charles T. Wolfe, Ghent University, Belgium Philippe Huneman, IHPST (CNRS/Université Paris I Panthéon-Sorbonne), France Thomas A.C. Reydon, Leibniz Universität Hannover, Germany Editorial Board Marshall Abrams (University of Alabama at Birmingham) Andre Ariew (Missouri) Minus van Baalen (UPMC, Paris) Domenico Bertoloni Meli (Indiana) Richard Burian (Virginia Tech) Pietro Corsi (EHESS, Paris) François Duchesneau (Université de Montréal) John Dupré (Exeter) Paul Farber (Oregon State) Lisa Gannett (Saint Mary’s University, Halifax) Andy Gardner (Oxford) Paul Griffi ths (Sydney) Jean Gayon (IHPST, Paris) Guido Giglioni (Warburg Institute, London) Thomas Heams (INRA, AgroParisTech, Paris) James Lennox (Pittsburgh) Annick Lesne (CNRS, UPMC, Paris) Tim Lewens (Cambridge) Edouard Machery (Pittsburgh) Alexandre Métraux (Archives Poincaré, Nancy) Hans Metz (Leiden) Roberta Millstein (Davis) Staffan Müller-Wille (Exeter) Dominic Murphy (Sydney) François Munoz (Université Montpellier 2) Stuart Newman (New York Medical College) Frederik Nijhout (Duke) Samir Okasha (Bristol) Susan Oyama (CUNY) Kevin Padian (Berkeley) David Queller (Washington University, St Louis) Stéphane Schmitt (SPHERE, CNRS, Paris) Phillip Sloan (Notre Dame) Jacqueline Sullivan -
Photophysics of Structural Color in the Morpho Butterflies
Original Paper________________________________________________________ Forma, 17, 103–121, 2002 Photophysics of Structural Color in the Morpho Butterflies Shuichi KINOSHITA1,2*, Shinya YOSHIOKA1,2, Yasuhiro FUJII2 and Naoko OKAMOTO1 1Graduate School of Frontier Biosciences, Osaka University, Machikaneyama 1-1, Toyonaka, Osaka 560-0043, Japan 2Department of Physics, Graduate School of Science, Osaka University, Machikaneyama 1-1, Toyonaka, Osaka 560-0043, Japan *E-mail address: [email protected] (Received April 23, 2002; Accepted May 30, 2002) Keywords: Structural Color, Iridescence, Morpho Butterfly, Interference, Diffraction Abstract. The Morpho butterflies exhibit surprisingly brilliant blue wings originating from the submicron structure created on scales of the wing. It shows extraordinarily uniform color with respect to the observation direction which cannot be explained using a simple multilayer interference model. We have performed microscopic, optical and theoretical investigations on the wings of four Morpho species and have found separate lamellar structure with irregular heights is extremely important. Using a simple model, we have shown that the combined action of interference and diffraction is essential for the structural color. It is also shown that the presence of pigment beneath the iridescent scales greatly enhances the blue coloring by reducing the unwanted background light. Further, variations of color tones and gloss in the Morpho wings are discussed in terms of the combination of cover and ground scales with various structures and functions. 1. Introduction Coloring in nature mostly comes from the inherent colors of materials, but it sometimes has a purely physical origin, such as diffraction or interference of light. The latter, called structural color or iridescence, has long been a problem of scientific interest (PARKER, 2000). -
Interspecific Social Dominance Mimicry in Birds
bs_bs_banner Zoological Journal of the Linnean Society, 2014. With 6 figures Interspecific social dominance mimicry in birds RICHARD OWEN PRUM1,2* 1Department of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520-8150, USA 2Peabody Natural History Museum, Yale University, New Haven, CT 06520-8150, USA Received 3 May 2014; revised 17 June 2014; accepted for publication 21 July 2014 Interspecific social dominance mimicry (ISDM) is a proposed form of social parasitism in which a subordinate species evolves to mimic and deceive a dominant ecological competitor in order to avoid attack by the dominant, model species. The evolutionary plausibility of ISDM has been established previously by the Hairy-Downy game (Prum & Samuelson). Psychophysical models of avian visual acuity support the plausibility of visual ISDM at distances ∼>2–3 m for non-raptorial birds, and ∼>20 m for raptors. Fifty phylogenetically independent examples of avian ISDM involving 60 model and 93 mimic species, subspecies, and morphs from 30 families are proposed and reviewed. Patterns of size differences, phylogeny, and coevolutionary radiation generally support the predic- tions of ISDM. Mimics average 56–58% of the body mass of the proposed model species. Mimics may achieve a large potential deceptive social advantage with <20% reduction in linear body size, which is well within the range of plausible, visual size confusion. Several, multispecies mimicry complexes are proposed (e.g. kiskadee- type flycatchers) which may coevolve through hierarchical variation in the deceptive benefits, similar to Müllerian mimicry. ISDM in birds should be tested further with phylogenetic, ecological, and experimental investigations of convergent similarity in appearance, ecological competition, and aggressive social interactions between sympatric species. -
Coloration Mechanisms and Phylogeny of Morpho Butterflies M
© 2016. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2016) 219, 3936-3944 doi:10.1242/jeb.148726 RESEARCH ARTICLE Coloration mechanisms and phylogeny of Morpho butterflies M. A. Giraldo1,*, S. Yoshioka2, C. Liu3 and D. G. Stavenga4 ABSTRACT scales (Ghiradella, 1998). The ventral wing side of Morpho Morpho butterflies are universally admired for their iridescent blue butterflies is studded by variously pigmented scales, together coloration, which is due to nanostructured wing scales. We performed creating a disruptive pattern that may provide camouflage when the a comparative study on the coloration of 16 Morpho species, butterflies are resting with closed wings. When flying, Morpho investigating the morphological, spectral and spatial scattering butterflies display the dorsal wing sides, which are generally bright- properties of the differently organized wing scales. In numerous blue in color. The metallic reflecting scales have ridges consisting of previous studies, the bright blue Morpho coloration has been fully a stack of slender plates, the lamellae, which in cross-section show a attributed to the multi-layered ridges of the cover scales’ upper Christmas tree-like structure (Ghiradella, 1998). This structure is not laminae, but we found that the lower laminae of the cover and ground exclusive to Morpho butterflies and has also been found in other scales play an important additional role, by acting as optical thin film butterfly species, for instance pierids, reflecting in the blue and/or reflectors. We conclude that Morpho coloration is a subtle UV wavelength range (Ghiradella et al., 1972; Rutowski et al., combination of overlapping pigmented and/or unpigmented scales, 2007; Giraldo et al., 2008). -
Tympanal Ears in Nymphalidae Butterflies: Morphological Diversity and Tests on the Function of Hearing
Tympanal Ears in Nymphalidae Butterflies: Morphological Diversity and Tests on the Function of Hearing by Laura E. Hall A thesis submitted to the Faculty of Graduate Studies and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Master of Science in Biology Carleton University Ottawa, Ontario, Canada © 2014 Laura E. Hall i Abstract Several Nymphalidae butterflies possess a sensory structure called the Vogel’s organ (VO) that is proposed to function in hearing. However, little is known about the VO’s structure, taxonomic distribution or function. My first research objective was to examine VO morphology and its accessory structures across taxa. Criteria were established to categorize development levels of butterfly VOs and tholi. I observed that enlarged forewing veins are associated with the VOs of several species within two subfamilies of Nymphalidae. Further, I discovered a putative light/temperature-sensitive organ associated with the VOs of several Biblidinae species. The second objective was to test the hypothesis that insect ears function to detect bird flight sounds for predator avoidance. Neurophysiological recordings collected from moth ears show a clear response to flight sounds and chirps from a live bird in the laboratory. Finally, a portable electrophysiology rig was developed to further test this hypothesis in future field studies. ii Acknowledgements First and foremost I would like to thank David Hall who spent endless hours listening to my musings and ramblings regarding butterfly ears, sharing in the joy of my discoveries, and comforting me in times of frustration. Without him, this thesis would not have been possible. I thank Dr. -
Evolution of the Morphological Innovations of Feathers RICHARD O
JOURNAL OF EXPERIMENTAL ZOOLOGY (MOL DEV EVOL) 304B:570–579 (2005) Evolution of the Morphological Innovations of Feathers RICHARD O. PRUMÃ Department of Ecology and Evolutionary Biology and Peabody Museum of Natural History, Yale University, New Haven, Connecticut 06520 ABSTRACT Feathers are complex assemblages of multiple morphological innovations. Recent research on the development and evolution of feathers has produced new insights into the origin and diversification of the morphological innovations in feathers. In this article, I review and discuss the contribution of three different factors to the evolution of morphological innovations in feathers: feather tubularity, hierarchical morphological modularity, and the co-option molecular signaling modules. The developing feather germ is a tube of epidermis with a central dermal pulp. The tubular organization of the feather germ and follicle produces multiple axes over which morphological differentiation can be organized. Feather complexity is organized into a hierarchy of morphological modules. These morphological modules evolved through the innovative differentiation along multiple different morphological axes created by the tubular feather germ. Concurrently, many of the morphological innovations of feathers evolved through the evolutionary co-option of plesiomorphic molecular signaling modules. Gene co-option also reveals a role for contingency in the evolution of hierarchical morphological innovations. J. Exp. Zool. (Mol. Dev. Evol.) 304B:570– 579, 2005. r 2005 Wiley-Liss, Inc. Feathers are an outstanding example of a is exploited for a wide variety of functions in the hierarchically complex morphological innovation lives of birds, and their theropod ancestors (Prum (Prum, ’99; Prum and Dyck, 2003). As the other and Brush, 2002), including flight, insulation, articles in this symposium emphasize, the origin of visual communication, crypsis, and even sound morphological innovations, or evolutionary novel- production and water transport (Stettenheim, ties, provides special challenges to the field of ’76). -
K & K Imported Butterflies
K & K Imported Butterflies www.importedbutterflies.com Ken Werner Owners Kraig Anderson 4075 12 TH AVE NE 12160 Scandia Trail North Naples Fl. 34120 Scandia, MN. 55073 239-353-9492 office 612-961-0292 cell 239-404-0016 cell 651-269-6913 cell 239-353-9492 fax 651-433-2482 fax [email protected] [email protected] Other companies Gulf Coast Butterflies Spineless Wonders Supplier of Consulting and Construction North American Butterflies of unique Butterfly Houses, and special events Exotic Butterfly and Insect list North American Butterfly list This a is a complete list of K & K Imported Butterflies We are also in the process on adding new species, that have never been imported and exhibited in the United States You will need to apply for an interstate transport permit to get the exotic species from any domestic distributor. We will be happy to assist you in any way with filling out the your PPQ526 Thank You Kraig and Ken There is a distinction between import and interstate permits. The two functions/activities can not be on one permit. You are working with an import permit, thus all of the interstate functions are blocked. If you have only a permit to import you will need to apply for an interstate transport permit to get the very same species from a domestic distributor. If you have an import permit (or any other permit), you can go into your ePermits account and go to my applications, copy the application that was originally submitted, thus a Duplicate application is produced. Then go into the "Origination Point" screen, select the "Change Movement Type" button. -
Morpho Butterfly Scales
Bioinspired, Biomimetic and Nanobiomaterials Pages 68–72 http://dx.doi.org/10.1680/bbn.14.00026 Volume 4 Issue BBN1 Memorial Issue Short Communication Received 25/06/2014 Accepted 28/07/2014 Making photonic structures via cell culture: Published online 03/08/2014 Morpho butterfly scales Keywords: biomimetics\cell culture\development\nanostructu res\natural photonics\Morpho butterfly Parker and Townley ice | science ICE Publishing: All rights reserved Making photonic structures via cell culture: Morpho butterfly scales 1 Andrew Richard Parker* 2 Helen Elizabeth Townley Research Leader, Department of Life Sciences, Natural History Senior Research Fellow, Department of Engineering Science, Museum, London, UK University of Oxford, Oxford, UK 1 2 The photonic structures that cause the electric blue colour of some Morpho butterflies are desirable within industry. They have been reproduced on very small areas to produce prototype biomimetic structures, yet there is currently no technique to accurately manufacture these structures at a commercial level. Here, tissue and cell culture techniques are explored as a possible method of producing large quantities of the blue scales of Morpho peliedes. This represents the first attempt to culture the wing scales of aMorpho butterfly, and many problems were encountered. These could be remedied in future studies, but it is concluded that cell culture is probably not a viable technique to provide the Morpho structure for industry in the near future. However, tissue culture experiments revealed important results of scale development. 1. Introduction (Figure 1). Often this colour-generating scale is covered by another Animals and plants boast a range of sub-micron photonic devices, scale, which serves to further scatter the light.