Checklist of the Sphinx Moths of Arkansas Leo J
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Genome Analysis of a Novel Clade B Betabaculovirus Isolated from the Legume Pest Matsumuraeses Phaseoli (Lepidoptera: Tortricidae)
viruses Article Genome Analysis of a Novel Clade b Betabaculovirus Isolated from the Legume Pest Matsumuraeses phaseoli (Lepidoptera: Tortricidae) Ruihao Shu 1, Qian Meng 1, Lin Miao 1, Hongbin Liang 2, Jun Chen 2, Yuan Xu 2, Luqiang Cheng 1,3, Wenyi Jin 1,4, Qilian Qin 1 and Huan Zhang 1,* 1 State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; [email protected] (R.S.); [email protected] (Q.M.); [email protected] (L.M.); [email protected] (L.C.); [email protected] (W.J.); [email protected] (Q.Q.) 2 National Animal Collection Resource Center, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China; [email protected] (H.L.); [email protected] (J.C.); [email protected] (Y.X.) 3 College of Horticulture and Plant Protection, Yangzhou University, Yangzhou 225009, China 4 College of Life Sciences, Hebei University, Baoding 071002, China * Correspondence: [email protected] Received: 25 August 2020; Accepted: 20 September 2020; Published: 23 September 2020 Abstract: Matsumuraeses phaseoli is a Lepidopteran pest that primarily feeds on numerous species of cultivated legumes, such as Glycine and Phaseolus. It is widely distributed in northeast Asia. A novel granulovirus, designated as Matsumuraeses phaseoli granulovirus (MaphGV), was isolated from pathogenic M. phaseoli larvae that dwell in rolled leaves of Astragalus membranaceus, a Chinese medicinal herb. In this study, using next-generation sequencing, we report the complete genome of MaphGV. MaphGV genome comprises a double-stranded DNA of 116,875 bp, with 37.18% GC content. -
Perspective Where Might Be Many Tropical Insects?
Biological Conservation 233 (2019) 102–108 Contents lists available at ScienceDirect Biological Conservation journal homepage: www.elsevier.com/locate/biocon Perspective Perspective: Where might be many tropical insects? T ⁎ Daniel H. Janzen , Winnie Hallwachs Department of Biology, University of Pennsylvania, Philadelphia 19104, United States of America ABSTRACT I have been watching the gradual and very visible decline of Mexican and Central American insect density and species richness since 1953 and Winnie since 1978. The loss is very real for essentially all higher taxa, and the reasons are very evident: intense forest and agricultural simplification of very large areas, massive use of pesticides, habitat fragmentation, and at least since the 1980's, ever-increasing climate change in temperature, rainfall, and synchronization of seasonal cues. There is no ecological concept suggesting that this biodiversity and habitat impoverishment is restricted to this portion of the Neotropics, and our 50 years of occasional visits to other parts of the tropics suggest the same. We are losing most of the insect community that is still in the cloud forests due to the drying of the tops of tropical mountains, just as we are losing the huge expanses of insect communities that once occupied the fertile soils, weather, and water of the lowland tropics. Today we have unimaginable access to the world's biodiversity through the internet, roads, dwellings, education, bioliterate societies, DNA barcoding, genome sequencing, and human curiosity. The wild world gains from our understanding that it needs large and diverse terrain, relief from hunting trees and animals, site-specific restoration, profit-sharing with its societies, and tolerance of humans and our extended genomes. -
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11 -
Lepidoptera Sphingidae:) of the Caatinga of Northeast Brazil: a Case Study in the State of Rio Grande Do Norte
212212 JOURNAL OF THE LEPIDOPTERISTS’ SOCIETY Journal of the Lepidopterists’ Society 59(4), 2005, 212–218 THE HIGHLY SEASONAL HAWKMOTH FAUNA (LEPIDOPTERA SPHINGIDAE:) OF THE CAATINGA OF NORTHEAST BRAZIL: A CASE STUDY IN THE STATE OF RIO GRANDE DO NORTE JOSÉ ARAÚJO DUARTE JÚNIOR Programa de Pós-Graduação em Ciências Biológicas, Departamento de Sistemática e Ecologia, Universidade Federal da Paraíba, 58059-900, João Pessoa, Paraíba, Brasil. E-mail: [email protected] AND CLEMENS SCHLINDWEIN Departamento de Botânica, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, s/n, Cidade Universitária, 50670-901, Recife, Pernambuco, Brasil. E-mail:[email protected] ABSTRACT: The caatinga, a thorn-shrub succulent savannah, is located in Northeastern Brazil and characterized by a short and irregular rainy season and a severe dry season. Insects are only abundant during the rainy months, displaying a strong seasonal pat- tern. Here we present data from a yearlong Sphingidae survey undertaken in the reserve Estação Ecológica do Seridó, located in the state of Rio Grande do Norte. Hawkmoths were collected once a month during two subsequent new moon nights, between 18.00h and 05.00h, attracted with a 160-watt mercury vapor light. A total of 593 specimens belonging to 20 species and 14 genera were col- lected. Neogene dynaeus, Callionima grisescens, and Hyles euphorbiarum were the most abundant species, together comprising up to 82.2% of the total number of specimens collected. These frequent species are residents of the caatinga of Rio Grande do Norte. The rare Sphingidae in this study, Pseudosphinx tetrio, Isognathus australis, and Cocytius antaeus, are migratory species for the caatinga. -
The Sphingidae (Lepidoptera) of the Philippines
©Entomologischer Verein Apollo e.V. Frankfurt am Main; download unter www.zobodat.at Nachr. entomol. Ver. Apollo, Suppl. 17: 17-132 (1998) 17 The Sphingidae (Lepidoptera) of the Philippines Willem H o g e n e s and Colin G. T r e a d a w a y Willem Hogenes, Zoologisch Museum Amsterdam, Afd. Entomologie, Plantage Middenlaan 64, NL-1018 DH Amsterdam, The Netherlands Colin G. T readaway, Entomologie II, Forschungsinstitut Senckenberg, Senckenberganlage 25, D-60325 Frankfurt am Main, Germany Abstract: This publication covers all Sphingidae known from the Philippines at this time in the form of an annotated checklist. (A concise checklist of the species can be found in Table 4, page 120.) Distribution maps are included as well as 18 colour plates covering all but one species. Where no specimens of a particular spe cies from the Philippines were available to us, illustrations are given of specimens from outside the Philippines. In total we have listed 117 species (with 5 additional subspecies where more than one subspecies of a species exists in the Philippines). Four tables are provided: 1) a breakdown of the number of species and endemic species/subspecies for each subfamily, tribe and genus of Philippine Sphingidae; 2) an evaluation of the number of species as well as endemic species/subspecies per island for the nine largest islands of the Philippines plus one small island group for comparison; 3) an evaluation of the Sphingidae endemicity for each of Vane-Wright’s (1990) faunal regions. From these tables it can be readily deduced that the highest species counts can be encountered on the islands of Palawan (73 species), Luzon (72), Mindanao, Leyte and Negros (62 each). -
Hawk Moths of North America Is Richly Illustrated with Larval Images and Contains an Abundance of Life History Information
08 caterpillars EUSA/pp244-273 3/9/05 6:37 PM Page 244 244 TULIP-TREE MOTH CECROPIA MOTH 245 Callosamia angulifera Hyalophora cecropia RECOGNITION Frosted green with shiny yellow, orange, and blue knobs over top and sides of body. RECOGNITION Much like preceding but paler or Dorsal knobs on T2, T3, and A1 somewhat globular and waxier in color with pale stripe running below set with black spinules. Paired knobs on A2–A7 more spiracles on A1–A10 and black dots on abdomen cylindrical, yellow; knob over A8 unpaired and rounded. lacking contrasting pale rings. Yellow abdominal Larva to 10cm. Caterpillars of larch-feeding Columbia tubercle over A8 short, less than twice as high as broad. Silkmoth (Hyalophora columbia) have yellow-white to Larva to 6cm. Sweetbay Silkmoth (Callosamia securifera) yellow-pink instead of bright yellow knobs over dorsum similar in appearance but a specialist on sweet bay. Its of abdomen and knobs along sides tend to be more white than blue (as in Cecropia) and are yellow abdominal tubercle over A8 is nearly three times as set in black bases (see page 246). long as wide and the red knobs over thorax are cylindrical (see page 246). OCCURRENCE Urban and suburban yards and lots, orchards, fencerows, woodlands, OCCURRENCE Woodlands and forests from Michigan, southern Ontario, and and forests from Canada south to Florida and central Texas. One generation with mature Massachusetts to northern Florida and Mississippi. One principal generation northward; caterpillars from late June through August over most of range. two broods in South with mature caterpillars from early June onward. -
Conservation and Management of Eastern Big-Eared Bats a Symposium
Conservation and Management of Eastern Big-eared Bats A Symposium y Edited b Susan C. Loeb, Michael J. Lacki, and Darren A. Miller U.S. Department of Agriculture Forest Service Southern Research Station General Technical Report SRS-145 DISCLAIMER The use of trade or firm names in this publication is for reader information and does not imply endorsement by the U.S. Department of Agriculture of any product or service. Papers published in these proceedings were submitted by authors in electronic media. Some editing was done to ensure a consistent format. Authors are responsible for content and accuracy of their individual papers and the quality of illustrative materials. Cover photos: Large photo: Craig W. Stihler; small left photo: Joseph S. Johnson; small middle photo: Craig W. Stihler; small right photo: Matthew J. Clement. December 2011 Southern Research Station 200 W.T. Weaver Blvd. Asheville, NC 28804 Conservation and Management of Eastern Big-eared Bats: A Symposium Athens, Georgia March 9–10, 2010 Edited by: Susan C. Loeb U.S Department of Agriculture Forest Service Southern Research Station Michael J. Lacki University of Kentucky Darren A. Miller Weyerhaeuser NR Company Sponsored by: Forest Service Bat Conservation International National Council for Air and Stream Improvement (NCASI) Warnell School of Forestry and Natural Resources Offield Family Foundation ContEntS Preface . v Conservation and Management of Eastern Big-Eared Bats: An Introduction . 1 Susan C. Loeb, Michael J. Lacki, and Darren A. Miller Distribution and Status of Eastern Big-eared Bats (Corynorhinus Spp .) . 13 Mylea L. Bayless, Mary Kay Clark, Richard C. Stark, Barbara S. -
2017, Jones Road, Near Blackhawk, RAIN (Photo: Michael Dawber)
Edited and Compiled by Rick Cavasin and Jessica E. Linton Toronto Entomologists’ Association Occasional Publication # 48-2018 European Skippers mudpuddling, July 6, 2017, Jones Road, near Blackhawk, RAIN (Photo: Michael Dawber) Dusted Skipper, April 20, 2017, Ipperwash Beach, LAMB American Snout, August 6, 2017, (Photo: Bob Yukich) Dunes Beach, PRIN (Photo: David Kaposi) ISBN: 978-0-921631-53-7 Ontario Lepidoptera 2017 Edited and Compiled by Rick Cavasin and Jessica E. Linton April 2018 Published by the Toronto Entomologists’ Association Toronto, Ontario Production by Jessica Linton TORONTO ENTOMOLOGISTS’ ASSOCIATION Board of Directors: (TEA) Antonia Guidotti: R.O.M. Representative Programs Coordinator The TEA is a non-profit educational and scientific Carolyn King: O.N. Representative organization formed to promote interest in insects, to Publicity Coordinator encourage cooperation among amateur and professional Steve LaForest: Field Trips Coordinator entomologists, to educate and inform non-entomologists about insects, entomology and related fields, to aid in the ONTARIO LEPIDOPTERA preservation of insects and their habitats and to issue Published annually by the Toronto Entomologists’ publications in support of these objectives. Association. The TEA is a registered charity (#1069095-21); all Ontario Lepidoptera 2017 donations are tax creditable. Publication date: April 2018 ISBN: 978-0-921631-53-7 Membership Information: Copyright © TEA for Authors All rights reserved. No part of this publication may be Annual dues: reproduced or used without written permission. Individual-$30 Student-free (Association finances permitting – Information on submitting records, notes and articles to beyond that, a charge of $20 will apply) Ontario Lepidoptera can be obtained by contacting: Family-$35 Jessica E. -
Bug of the Month by Jim Revell / November 2016 Eumorpha Pandorus | Pandora Sphinx
Bug of the Month by Jim Revell / November 2016 Eumorpha pandorus | Pandora Sphinx Eumorpha pandorus Pandora Sphinx Class: Insecta (Insects) Order: Lepidoptera Family: Sphingidae (Sphinx Moths) Genus: Eumorpha Species: pandorus (Pandora Sphinx) I love the phrase by Duke Elsner of Michigan State University Extension. In his post, he called the Sphinx Moth Caterpillars “the big cats of the vineyard.” How true it is! A member of the Hornworm group, one of these was found on my grapevines in September by a visiting MG Trainee. The caterpillar comes in green, orange, pink and cinnamon-to-dark brown. The one found on my grapevines was cinnamon-to-dark brown. The photo at top right shows this coloration and was taken by Maryann Frazier at Penn State Entomology Extension. Distinguishing marks and notes regarding this interesting caterpillar: They are large and can reach over five inches in length. They have pale-to-yellow spots surrounding spiracles A3-A7 (my caterpillar had white markings). In early to middle instars, the rear horn is thin and coiled. In the last instar, the horn is replaced by a button which resembles an eye-spot. These “cats” are feisty and will whip their front body part back and forth, regurgitating food to try and stop predators (including humans) from attacking. They feed on peppervine, grapevine and Virginia Creeper. Upon reaching maturity, the “cats” tunnel into the soil and build pupation chambers several inches below ground. In sandy soil, these chambers may be a foot below surface. The cocoons are reddish brown to dark brown and can be two inches in length. -
Lake Worth Lagoon
TABLE OF CONTENTS INTRODUCTION ................................................................................ 1 PURPOSE AND SIGNIFICANCE OF THE PARK ...................................... 1 Park Significance .............................................................................. 1 PURPOSE AND SCOPE OF THE PLAN ................................................... 2 MANAGEMENT PROGRAM OVERVIEW ................................................. 7 Management Authority and Responsibility ............................................ 7 Park Management Goals .................................................................... 8 Management Coordination ................................................................. 8 Public Participation ........................................................................... 9 Other Designations ........................................................................... 9 RESOURCE MANAGEMENT COMPONENT INTRODUCTION .............................................................................. 15 RESOURCE DESCRIPTION AND ASSESSMENT ................................... 15 Natural Resources .......................................................................... 16 Topography ............................................................................... 20 Geology .................................................................................... 21 Soils ......................................................................................... 21 Minerals ................................................................................... -
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes
Phylogeny and Biogeography of Hawkmoths (Lepidoptera: Sphingidae): Evidence from Five Nuclear Genes Akito Y. Kawahara1*, Andre A. Mignault1, Jerome C. Regier2, Ian J. Kitching3, Charles Mitter1 1 Department of Entomology, College Park, Maryland, United States of America, 2 Center for Biosystems Research, University of Maryland Biotechnology Institute, College Park, Maryland, United States of America, 3 Department of Entomology, The Natural History Museum, London, United Kingdom Abstract Background: The 1400 species of hawkmoths (Lepidoptera: Sphingidae) comprise one of most conspicuous and well- studied groups of insects, and provide model systems for diverse biological disciplines. However, a robust phylogenetic framework for the family is currently lacking. Morphology is unable to confidently determine relationships among most groups. As a major step toward understanding relationships of this model group, we have undertaken the first large-scale molecular phylogenetic analysis of hawkmoths representing all subfamilies, tribes and subtribes. Methodology/Principal Findings: The data set consisted of 131 sphingid species and 6793 bp of sequence from five protein-coding nuclear genes. Maximum likelihood and parsimony analyses provided strong support for more than two- thirds of all nodes, including strong signal for or against nearly all of the fifteen current subfamily, tribal and sub-tribal groupings. Monophyly was strongly supported for some of these, including Macroglossinae, Sphinginae, Acherontiini, Ambulycini, Philampelini, Choerocampina, and Hemarina. Other groupings proved para- or polyphyletic, and will need significant redefinition; these include Smerinthinae, Smerinthini, Sphingini, Sphingulini, Dilophonotini, Dilophonotina, Macroglossini, and Macroglossina. The basal divergence, strongly supported, is between Macroglossinae and Smerinthinae+Sphinginae. All genes contribute significantly to the signal from the combined data set, and there is little conflict between genes. -
Archiv Für Naturgeschichte
© Biodiversity Heritage Library, http://www.biodiversitylibrary.org/; www.zobodat.at Lepidoptera für 1903. Bearbeitet von Dr. Robert Lucas in Rixdorf bei Berlin. A. Publikationen (Autoren alphabetisch) mit Referaten. Adkin, Robert. Pyrameis cardui, Plusia gamma and Nemophila noc- tuella. The Entomologist, vol. 36. p. 274—276. Agassiz, G. Etüde sur la coloration des ailes des papillons. Lausanne, H. Vallotton u. Toso. 8 °. 31 p. von Aigner-Abafi, A. (1). Variabilität zweier Lepidopterenarten. Verhandlgn. zool.-bot. Ges. Wien, 53. Bd. p. 162—165. I. Argynnis Paphia L. ; IL Larentia bilineata L. — (2). Protoparce convolvuli. Entom. Zeitschr. Guben. 17. Jahrg. p. 22. — (3). Über Mimikry. Gaea. 39. Jhg. p. 166—170, 233—237. — (4). A mimicryröl. Rov. Lapok, vol. X, p. 28—34, 45—53 — (5). A Mimicry. Allat. Kozl. 1902, p. 117—126. — (6). (Über Mimikry). Allgem. Zeitschr. f. Entom. 7. Bd. (Schluß p. 405—409). Über Falterarten, welche auch gesondert von ihrer Umgebung, in ruhendem Zustande eine eigentümliche, das Auge täuschende Form annehmen (Lasiocampa quercifolia [dürres Blatt], Phalera bucephala [zerbrochenes Ästchen], Calocampa exoleta [Stück morschen Holzes]. — [Stabheuschrecke, Acanthoderus]. Raupen, die Meister der Mimikry sind. Nachahmung anderer Tiere. Die Mimik ist in vielen Fällen zwecklos. — Die wenn auch recht geistreichen Mimikry-Theorien sind doch vielleicht nur ein müßiges Spiel der Phantasie. Aitken u. Comber, E. A list of the butterflies of the Konkau. Journ. Bombay Soc. vol. XV. p. 42—55, Suppl. p. 356. Albisson, J. Notes biologiques pour servir ä l'histoire naturelle du Charaxes jasius. Bull. Soc. Etud. Sc. nat. Nimes. T. 30. p. 77—82. Annandale u. Robinson. Siehe unter S w i n h o e.