Differential Investment in Visual and Olfactory Brain Areas Reflects Behavioural Choices in Hawk Moths
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Evolution of Insect Color Vision: from Spectral Sensitivity to Visual Ecology
EN66CH23_vanderKooi ARjats.cls September 16, 2020 15:11 Annual Review of Entomology Evolution of Insect Color Vision: From Spectral Sensitivity to Visual Ecology Casper J. van der Kooi,1 Doekele G. Stavenga,1 Kentaro Arikawa,2 Gregor Belušic,ˇ 3 and Almut Kelber4 1Faculty of Science and Engineering, University of Groningen, 9700 Groningen, The Netherlands; email: [email protected] 2Department of Evolutionary Studies of Biosystems, SOKENDAI Graduate University for Advanced Studies, Kanagawa 240-0193, Japan 3Department of Biology, Biotechnical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia; email: [email protected] 4Lund Vision Group, Department of Biology, University of Lund, 22362 Lund, Sweden; email: [email protected] Annu. Rev. Entomol. 2021. 66:23.1–23.28 Keywords The Annual Review of Entomology is online at photoreceptor, compound eye, pigment, visual pigment, behavior, opsin, ento.annualreviews.org anatomy https://doi.org/10.1146/annurev-ento-061720- 071644 Abstract Annu. Rev. Entomol. 2021.66. Downloaded from www.annualreviews.org Copyright © 2021 by Annual Reviews. Color vision is widespread among insects but varies among species, depend- All rights reserved ing on the spectral sensitivities and interplay of the participating photore- Access provided by University of New South Wales on 09/26/20. For personal use only. ceptors. The spectral sensitivity of a photoreceptor is principally determined by the absorption spectrum of the expressed visual pigment, but it can be modified by various optical and electrophysiological factors. For example, screening and filtering pigments, rhabdom waveguide properties, retinal structure, and neural processing all influence the perceived color signal. -
British Lepidoptera (/)
British Lepidoptera (/) Home (/) Anatomy (/anatomy.html) FAMILIES 1 (/families-1.html) GELECHIOIDEA (/gelechioidea.html) FAMILIES 3 (/families-3.html) FAMILIES 4 (/families-4.html) NOCTUOIDEA (/noctuoidea.html) BLOG (/blog.html) Glossary (/glossary.html) Family: SPHINGIDAE (3SF 13G 18S) Suborder:Glossata Infraorder:Heteroneura Superfamily:Bombycoidea Refs: Waring & Townsend, Wikipedia, MBGBI9 Proboscis short to very long, unscaled. Antenna ~ 1/2 length of forewing; fasciculate or pectinate in male, simple in female; apex pointed. Labial palps long, 3-segmented. Eye large. Ocelli absent. Forewing long, slender. Hindwing ±triangular. Frenulum and retinaculum usually present but may be reduced. Tegulae large, prominent. Leg spurs variable but always present on midtibia. 1st tarsal segment of mid and hindleg about as long as tibia. Subfamily: Smerinthinae (3G 3S) Tribe: Smerinthini Probably characterised by a short proboscis and reduced or absent frenulum Mimas Smerinthus Laothoe 001 Mimas tiliae (Lime Hawkmoth) 002 Smerinthus ocellata (Eyed Hawkmoth) 003 Laothoe populi (Poplar Hawkmoth) (/002- (/001-mimas-tiliae-lime-hawkmoth.html) smerinthus-ocellata-eyed-hawkmoth.html) (/003-laothoe-populi-poplar-hawkmoth.html) Subfamily: Sphinginae (3G 4S) Rest with wings in tectiform position Tribe: Acherontiini Agrius Acherontia 004 Agrius convolvuli 005 Acherontia atropos (Convolvulus Hawkmoth) (Death's-head Hawkmoth) (/005- (/004-agrius-convolvuli-convolvulus- hawkmoth.html) acherontia-atropos-deaths-head-hawkmoth.html) Tribe: Sphingini Sphinx (2S) -
A Survey on Sphingidae (Lepidoptera) Species of South Eastern Turkey
Cumhuriyet Science Journal e-ISSN: 2587-246X Cumhuriyet Sci. J., 41(1) (2020) 319-326 ISSN: 2587-2680 http://dx.doi.org/10.17776/csj.574903 A survey on sphingidae (lepidoptera) species of south eastern Turkey with new distributional records Erdem SEVEN 1 * 1 Department of Gastronomy and Culinary Arts, School of Tourism and Hotel Management, Batman University, 72060, Batman, Turkey. Abstract Article info History: This paper provides comments on the Sphingidae species of south eastern Turkey by the field Received:10.06.2019 surveys are conducted between in 2015-2017. A total of 15 species are determined as a result Accepted:20.12.2019 of the investigations from Batman, Diyarbakır and Mardin provinces. With this study, the Keywords: number of sphinx moths increased to 13 in Batman, 14 in Diyarbakır and 8 in Mardin. Among Fauna, them, 7 species for Batman, 4 species for Diyarbakır and 1 species for Mardin are new record. Hawk moths, For each species, original reference, type locality, material examined, distribution in the world New records, and in Turkey, and larval hostplants are given. Adults figures of Smerinthus kindermanni Sphingidae, Lederer, 1852; Marumba quercus ([Denis & Schiffermüller], 1775); Rethera komarovi Turkey. (Christoph, 1885); Macroglossum stellatarum (Linnaeus, 1758); Hyles euphorbiae (Linnaeus, 1758) and H. livornica (Esper, [1780]) are illustrated. 1. Introduction 18, 22-24]: Acherontia atropos (Linnaeus, 1758); Agrius convolvuli (Linnaeus, 1758); Akbesia davidi (Oberthür, 1884); Clarina kotschyi (Kollar, [1849]); C. The Sphingidae family classified in the Sphingoidea syriaca (Lederer, 1855); Daphnis nerii (Linnaeus, Superfamily and species of the family are generally 1758); Deilephila elpenor (Linnaeus, 1758); D. -
The Brain of a Nocturnal Migratory Insect, the Australian Bogong Moth
bioRxiv preprint doi: https://doi.org/10.1101/810895; this version posted January 21, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. The brain of a nocturnal migratory insect, the Australian Bogong moth Authors: Andrea Adden1, Sara Wibrand1, Keram Pfeiffer2, Eric Warrant1, Stanley Heinze1,3 1 Lund Vision Group, Lund University, Sweden 2 University of Würzburg, Germany 3 NanoLund, Lund University, Sweden Correspondence: [email protected] Abstract Every year, millions of Australian Bogong moths (Agrotis infusa) complete an astonishing journey: in spring, they migrate over 1000 km from their breeding grounds to the alpine regions of the Snowy Mountains, where they endure the hot summer in the cool climate of alpine caves. In autumn, the moths return to their breeding grounds, where they mate, lay eggs and die. These moths can use visual cues in combination with the geomagnetic field to guide their flight, but how these cues are processed and integrated in the brain to drive migratory behavior is unknown. To generate an access point for functional studies, we provide a detailed description of the Bogong moth’s brain. Based on immunohistochemical stainings against synapsin and serotonin (5HT), we describe the overall layout as well as the fine structure of all major neuropils, including the regions that have previously been implicated in compass-based navigation. The resulting average brain atlas consists of 3D reconstructions of 25 separate neuropils, comprising the most detailed account of a moth brain to date. -
Constant Neuropilar Ratio in the Insect Brain Alexey A
www.nature.com/scientificreports OPEN Constant neuropilar ratio in the insect brain Alexey A. Polilov* & Anastasia A. Makarova Revealing scaling rules is necessary for understanding the morphology, physiology and evolution of living systems. Studies of animal brains have revealed both general patterns, such as Haller’s rule, and patterns specifc for certain animal taxa. However, large-scale studies aimed at studying the ratio of the entire neuropil and the cell body rind in the insect brain have never been performed. Here we performed morphometric study of the adult brain in 37 insect species of 26 families and ten orders, ranging in volume from the smallest to the largest by a factor of more than 4,000,000, and show that all studied insects display a similar ratio of the volume of the neuropil to the cell body rind, 3:2. Allometric analysis for all insects shows that the ratio of the volume of the neuropil to the volume of the brain changes strictly isometrically. Analyses within particular taxa, size groups, and metamorphosis types also reveal no signifcant diferences in the relative volume of the neuropil; isometry is observed in all cases. Thus, we establish a new scaling rule, according to which the relative volume of the entire neuropil in insect brain averages 60% and remains constant. Large-scale studies of animal proportions supposedly started with the publication D’Arcy Wentworth Tompson’s book Growth and Forms1. In fact, the frst studies on the subject appeared long before the book (e.g.2), but it was Tomson’s work that laid the foundations for this discipline, which, following the studies of Julian Huxley 3,4, became a major fundamental and applied area of science5–8. -
Hawk-Moths, Family Sphingidae and Forewings Browner
Hawk-moths, Family Sphingidae and forewings browner. Wings normally held roof-wise along the body when at rest. Distinctive medium to large moths. Power• Larva green, striped with brown. ful fliers, generally with rather narrow, Habitat More sedentary than above pointed forewings. Most larvae are large, species, living mainly in rough flowery striped, and have a 'horn' at the tail end. places where Privet occurs. Status and distributfon Local in S Convolvulus Hawk-moth Britain, widespread on the Continent. Agrilfs c()llu()lulfli Season 6-7. A strikingly large moth; wingspan up to 12cm. Forewings greyish, marbled; hind• Poplar Hawk-moth wings browner. The abdomen is striped La()th()c l)()fJlfli with red, white and black. The proboscis A medium-sized hawk-moth; wingspan up may be up to 13cm long! to 90mm. Wings greyish to pinkish-brown, Habitat A migrant into N Europe from broadly banded, with a single white mark in the Mediterranean area, which may occur the centre of the forewings. Hindwings wherever there are flowers, especially Petu• orange-red at base, usually concealed, and nia and Nicotiana. Breeds on Convolvulus, but show in front of forewings at rest. Larvae only rarely does so in N Europe. green with yellow stripes. Status and distribution Very variable in Habitat A variety of habitats, associated numbers, regularly reaching S England, but with Sallow, Poplar and Aspen. not necessarily going further. Status and distribution Widely distrib• Season 6-9. uted and moderately common throughout the region. Death's Head Hawk-Moth Season 5-9. Achcrontia atrofJos Similar species An extraordinary insect, unlike anything Pine Hawk-moth Hyloicus pinostri is also else. -
Implementation of a Volumetric 3D Standard Brain in Manduca Sexta
Anisometric Brain Dimorphism Revisited: Implementation of a Volumetric 3D Standard Brain in Manduca sexta BASIL EL JUNDI, WOLF HUETTEROTH, ANGELA E. KURYLAS, AND JOACHIM SCHACHTNER* Department of Biology, Animal Physiology, Philipps-University, Marburg, Germany ABSTRACT labeled 10 female glomeruli that were homologous to pre- Lepidopterans like the giant sphinx moth Manduca sexta are viously quantitatively described male glomeruli including known for their conspicuous sexual dimorphism in the ol- the MGC. In summary, the neuropil volumes reveal an iso- factory system, which is especially pronounced in the an- metric sexual dimorphism in M. sexta brains. This propor- tennae and in the antennal lobe, the primary integration tional size difference between male and female brain neu- center of odor information. Even minute scents of female ropils masks an anisometric or disproportional dimorphism, pheromone are detected by male moths, facilitated by a which is restricted to the sex-related glomeruli of the an- huge array of pheromone receptors on their antennae. The tennal lobes and neither mirrored in other normal glomeruli associated neuropilar areas in the antennal lobe, the glo- nor in higher brain centers like the calyces of the mushroom meruli, are enlarged in males and organized in the form of bodies. Both the female and male 3D standard brain are also the so-called macroglomerular complex (MGC). In this study used for interspecies comparisons, and may serve as future we searched for anatomical sexual dimorphism more down- volumetric reference in pharmacological and behavioral ex- stream in the olfactory pathway and in other neuropil areas periments especially regarding development and adult plas- in the central brain. -
The Brain of a Nocturnal Migratory Insect, the Australian Bogong Moth
bioRxiv preprint doi: https://doi.org/10.1101/810895; this version posted January 21, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. The brain of a nocturnal migratory insect, the Australian Bogong moth Authors: Andrea Adden1, Sara Wibrand1, Keram Pfeiffer2, Eric Warrant1, Stanley Heinze1,3 1 Lund Vision Group, Lund University, Sweden 2 University of Würzburg, Germany 3 NanoLund, Lund University, Sweden Correspondence: [email protected] Abstract Every year, millions of Australian Bogong moths (Agrotis infusa) complete an astonishing journey: in spring, they migrate over 1000 km from their breeding grounds to the alpine regions of the Snowy Mountains, where they endure the hot summer in the cool climate of alpine caves. In autumn, the moths return to their breeding grounds, where they mate, lay eggs and die. These moths can use visual cues in combination with the geomagnetic field to guide their flight, but how these cues are processed and integrated in the brain to drive migratory behavior is unknown. To generate an access point for functional studies, we provide a detailed description of the Bogong moth’s brain. Based on immunohistochemical stainings against synapsin and serotonin (5HT), we describe the overall layout as well as the fine structure of all major neuropils, including the regions that have previously been implicated in compass-based navigation. The resulting average brain atlas consists of 3D reconstructions of 25 separate neuropils, comprising the most detailed account of a moth brain to date. -
Measuring Compound Eye Optics with Microscope and Microct Images
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.11.422154; this version posted December 12, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Title (<120 characters): Measuring Compound Eye Optics with Microscope and MicroCT Images 2 Article Type: Tools and Resources 3 Author Names and Affiliations: John Paul Currea1, Yash Sondhi2, Akito Y. Kawahara3, and Jamie 4 Theobald2 5 1Department of Psychology, Florida International University, Miami, FL 33199, U.S.A. 6 2Department of Biological Sciences, Florida International University, Miami, FL 33199, U.S.A. 7 3Florida Museum of Natural History, University of Florida, Gainesville, FL, 32611, U.S.A. 8 Abstract (<150 words): 9 The arthropod compound eye is the most prevalent eye type in the animal kingdom, with an impressive 10 range of shapes and sizes. Studying its natural range of morphologies provides insight into visual 11 ecology, development, and evolution. In contrast to the camera-type eyes we possess, external 12 structures of compound eyes often reveal resolution, sensitivity, and field of view if the eye is 13 spherical. Non-spherical eyes, however, require measuring internal structures using imaging 14 technology like MicroCT (µCT). Thus far, there is no efficient tool to automate characterizing 15 compound eye optics. We present two open-source programs: (1) the ommatidia detecting algorithm 16 (ODA), which automatically measures ommatidia count and diameter, and (2) a µCT pipeline, which 17 calculates anatomical acuity, sensitivity, and field of view across the eye by applying the ODA. -
A List of Cuban Lepidoptera (Arthropoda: Insecta)
TERMS OF USE This pdf is provided by Magnolia Press for private/research use. Commercial sale or deposition in a public library or website is prohibited. Zootaxa 3384: 1–59 (2012) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2012 · Magnolia Press ISSN 1175-5334 (online edition) A list of Cuban Lepidoptera (Arthropoda: Insecta) RAYNER NÚÑEZ AGUILA1,3 & ALEJANDRO BARRO CAÑAMERO2 1División de Colecciones Zoológicas y Sistemática, Instituto de Ecología y Sistemática, Carretera de Varona km 3. 5, Capdevila, Boyeros, Ciudad de La Habana, Cuba. CP 11900. Habana 19 2Facultad de Biología, Universidad de La Habana, 25 esq. J, Vedado, Plaza de La Revolución, La Habana, Cuba. 3Corresponding author. E-mail: rayner@ecologia. cu Table of contents Abstract . 1 Introduction . 1 Materials and methods. 2 Results and discussion . 2 List of the Lepidoptera of Cuba . 4 Notes . 48 Acknowledgments . 51 References . 51 Appendix . 56 Abstract A total of 1557 species belonging to 56 families of the order Lepidoptera is listed from Cuba, along with the source of each record. Additional literature references treating Cuban Lepidoptera are also provided. The list is based primarily on literature records, although some collections were examined: the Instituto de Ecología y Sistemática collection, Havana, Cuba; the Museo Felipe Poey collection, University of Havana; the Fernando de Zayas private collection, Havana; and the United States National Museum collection, Smithsonian Institution, Washington DC. One family, Schreckensteinidae, and 113 species constitute new records to the Cuban fauna. The following nomenclatural changes are proposed: Paucivena hoffmanni (Koehler 1939) (Psychidae), new comb., and Gonodontodes chionosticta Hampson 1913 (Erebidae), syn. -
An Investigation Into Australian Freshwater Zooplankton with Particular Reference to Ceriodaphnia Species (Cladocera: Daphniidae)
An investigation into Australian freshwater zooplankton with particular reference to Ceriodaphnia species (Cladocera: Daphniidae) Pranay Sharma School of Earth and Environmental Sciences July 2014 Supervisors Dr Frederick Recknagel Dr John Jennings Dr Russell Shiel Dr Scott Mills Table of Contents Abstract ...................................................................................................................................... 3 Declaration ................................................................................................................................. 5 Acknowledgements .................................................................................................................... 6 Chapter 1: General Introduction .......................................................................................... 10 Molecular Taxonomy ..................................................................................................... 12 Cytochrome C Oxidase subunit I ................................................................................... 16 Traditional taxonomy and cataloguing biodiversity ....................................................... 20 Integrated taxonomy ....................................................................................................... 21 Taxonomic status of zooplankton in Australia ............................................................... 22 Thesis Aims/objectives .................................................................................................. -
BUTTERFLY and MOTH (DK Eyewitness Books)
EYEWITNESS Eyewitness BUTTERFLY & MOTH BUTTERFLY & MOTH Eyewitness Butterfly & Moth Pyralid moth, Margaronia Smaller Wood Nymph butterfly, quadrimaculata ldeopsis gaura (China) (Indonesia) White satin moth caterpillar, Leucoma salicis (Europe & Asia) Noctuid moth, Eyed Hawkmoth Diphthera caterpillar, hieroglyphica Smerinthus ocellata (Central (Europe & Asia) America) Madagascan Moon Moth, Argema mittrei (Madagascar) Thyridid moth, Rhondoneura limatula (Madagascar) Red Glider butterfly, Cymothoe coccinata (Africa) Lasiocampid moth, Gloveria gargemella (North America) Tailed jay butterfly, Graphium agamemnon, (Asia & Australia) Jersey Tiger moth, Euplagia quadripunctaria (Europe & Asia) Arctiid moth, Composia credula (North & South America) Noctuid moth, Noctuid moth, Mazuca strigitincta Apsarasa radians (Africa) (India & Indonesia) Eyewitness Butterfly & Moth Written by PAUL WHALLEY Tiger Pierid butterfly, Birdwing butterfly, Dismorphia Troides hypolitus amphione (Indonesia) (Central & South America) Noctuid moth, Baorisa hieroglyphica (India & Southeast Asia) Hairstreak butterfly, Kentish Glory moth, Theritas coronata Endromis versicolora (South America) (Europe) DK Publishing, Inc. Peacock butterfly, Inachis io (Europe and Asia) LONDON, NEW YORK, MELBOURNE, MUNICH, and DELHI Project editor Michele Byam Managing art editor Jane Owen Special photography Colin Keates (Natural History Museum, London), Kim Taylor, and Dave King Editorial consultants Paul Whalley and the staff of the Natural History Museum Swallowtail butterfly This Eyewitness