Heteroptera: Pentatomidae
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Entomology of the Aucklands and Other Islands South of New Zealand: Lepidoptera, Ex Cluding Non-Crambine Pyralidae
Pacific Insects Monograph 27: 55-172 10 November 1971 ENTOMOLOGY OF THE AUCKLANDS AND OTHER ISLANDS SOUTH OF NEW ZEALAND: LEPIDOPTERA, EX CLUDING NON-CRAMBINE PYRALIDAE By J. S. Dugdale1 CONTENTS Introduction 55 Acknowledgements 58 Faunal Composition and Relationships 58 Faunal List 59 Key to Families 68 1. Arctiidae 71 2. Carposinidae 73 Coleophoridae 76 Cosmopterygidae 77 3. Crambinae (pt Pyralidae) 77 4. Elachistidae 79 5. Geometridae 89 Hyponomeutidae 115 6. Nepticulidae 115 7. Noctuidae 117 8. Oecophoridae 131 9. Psychidae 137 10. Pterophoridae 145 11. Tineidae... 148 12. Tortricidae 156 References 169 Note 172 Abstract: This paper deals with all Lepidoptera, excluding the non-crambine Pyralidae, of Auckland, Campbell, Antipodes and Snares Is. The native resident fauna of these islands consists of 42 species of which 21 (50%) are endemic, in 27 genera, of which 3 (11%) are endemic, in 12 families. The endemic fauna is characterised by brachyptery (66%), body size under 10 mm (72%) and concealed, or strictly ground- dwelling larval life. All species can be related to mainland forms; there is a distinctive pre-Pleistocene element as well as some instances of possible Pleistocene introductions, as suggested by the presence of pairs of species, one member of which is endemic but fully winged. A graph and tables are given showing the composition of the fauna, its distribution, habits, and presumed derivations. Host plants or host niches are discussed. An additional 7 species are considered to be non-resident waifs. The taxonomic part includes keys to families (applicable only to the subantarctic fauna), and to genera and species. -
(Pentatomidae) DISSERTATION Presented
Genome Evolution During Development of Symbiosis in Extracellular Mutualists of Stink Bugs (Pentatomidae) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Alejandro Otero-Bravo Graduate Program in Evolution, Ecology and Organismal Biology The Ohio State University 2020 Dissertation Committee: Zakee L. Sabree, Advisor Rachelle Adams Norman Johnson Laura Kubatko Copyrighted by Alejandro Otero-Bravo 2020 Abstract Nutritional symbioses between bacteria and insects are prevalent, diverse, and have allowed insects to expand their feeding strategies and niches. It has been well characterized that long-term insect-bacterial mutualisms cause genome reduction resulting in extremely small genomes, some even approaching sizes more similar to organelles than bacteria. While several symbioses have been described, each provides a limited view of a single or few stages of the process of reduction and the minority of these are of extracellular symbionts. This dissertation aims to address the knowledge gap in the genome evolution of extracellular insect symbionts using the stink bug – Pantoea system. Specifically, how do these symbionts genomes evolve and differ from their free- living or intracellular counterparts? In the introduction, we review the literature on extracellular symbionts of stink bugs and explore the characteristics of this system that make it valuable for the study of symbiosis. We find that stink bug symbiont genomes are very valuable for the study of genome evolution due not only to their biphasic lifestyle, but also to the degree of coevolution with their hosts. i In Chapter 1 we investigate one of the traits associated with genome reduction, high mutation rates, for Candidatus ‘Pantoea carbekii’ the symbiont of the economically important pest insect Halyomorpha halys, the brown marmorated stink bug, and evaluate its potential for elucidating host distribution, an analysis which has been successfully used with other intracellular symbionts. -
Chapter 12. Estimating the Host Range of the Tachinid Trichopoda Giacomellii, Introduced Into Australia for Biological Control of the Green Vegetable Bug
__________________________________ ASSESSING HOST RANGES OF PARASITOIDS AND PREDATORS CHAPTER 12. ESTIMATING THE HOST RANGE OF THE TACHINID TRICHOPODA GIACOMELLII, INTRODUCED INTO AUSTRALIA FOR BIOLOGICAL CONTROL OF THE GREEN VEGETABLE BUG M. Coombs CSIRO Entomology, 120 Meiers Road, Indooroopilly, Queensland, Australia 4068 [email protected] BACKGROUND DESCRIPTION OF PEST INVASION AND PROBLEM Nezara viridula (L.) is a cosmopolitan pest of fruit, vegetables, and field crops (Todd, 1989). The native geographic range of N. viridula is thought to include Ethiopia, southern Europe, and the Mediterranean region (Hokkanen, 1986; Jones, 1988). Other species in the genus occur in Africa and Asia (Freeman, 1940). First recorded in Australia in 1916, N. viridula soon be- came a widespread and serious pest of most legume crops, curcubits, potatoes, tomatoes, pas- sion fruit, sorghum, sunflower, tobacco, maize, crucifers, spinach, grapes, citrus, rice, and mac- adamia nuts (Hely et al., 1982; Waterhouse and Norris, 1987). In northern Victoria, central New South Wales, and southern Queensland, N. viridula is a serious pest of soybeans and pecans (Clarke, 1992; Coombs, 2000). Immature and adult bugs feed on vegetative buds, devel- oping and mature fruits, and seeds, causing reductions in crop quality and yield. The pest status of N. viridula in Australia is assumed to be partly due to the absence of parasitoids of the nymphs and adults. No native Australian tachinids have been found to parasitize N viridula effectively, although occasional oviposition and development of some species may occur (Cantrell, 1984; Coombs and Khan, 1997). Previous introductions of biological control agents to Australia for control of N. viridula include Trichopoda pennipes (Fabricius) and Trichopoda pilipes (Fabricius) (Diptera: Tachinidae), which are important parasitoids of N. -
Climate-Related Transboundary Pests and Diseases
HLC/08/BAK/4 CLIMATE-RELATED TRANSBOUNDARY PESTS AND DISEASES TECHNICAL BACKGROUND DOCUMENT FROM THE EXPERT CONSULTATION HELD ON 25 TO 27 FEBRUARY 2008 FAO, ROME CLIMATE CHANGE AND PEST DISEASES The movement of plant pests, animal diseases and invasive alien aquatic organisms across physical and political boundaries threatens food security and creates a global public concern across all countries and all regions. Countries allocate large resources to limit the spread and control of transboundary pests and diseases 1 such as avian influenza, foot-and-mouth disease and locust. They also adapt animal and plant health services and activities and cooperate regionally and globally for prevention, early warning and control. There is clear evidence that climate change is altering the distribution, incidence and intensity of animal and plant pests and diseases such as Bluetongue, a sheep disease that is moving north into more temperate zones of Europe. Cannon (see Annex 1) found examples of plant pests whose distribution is shifting in the United Kingdom and other parts of Europe, most likely due to climatic factors. For example, migrant moths of the Old World bollworm ( Helicoverpa armigera) had a phenomenal increase in the United Kingdom from 1969-2004 and there have been outbreaks at the northern edge of its range in Europe; cottony cushion scale ( Icerya purchasi) populations appear to be spreading northwards perhaps as a consequence of global warming; and cottony camellia scale ( Pulvinaria – Chloropulvinaria – floccifera) has become much more common in the United Kingdom, extending its range northwards in England and increasing its host range in the last decade or so, which is almost certainly in response to climate change. -
Kenai National Wildlife Refuge Species List, Version 2018-07-24
Kenai National Wildlife Refuge Species List, version 2018-07-24 Kenai National Wildlife Refuge biology staff July 24, 2018 2 Cover image: map of 16,213 georeferenced occurrence records included in the checklist. Contents Contents 3 Introduction 5 Purpose............................................................ 5 About the list......................................................... 5 Acknowledgments....................................................... 5 Native species 7 Vertebrates .......................................................... 7 Invertebrates ......................................................... 55 Vascular Plants........................................................ 91 Bryophytes ..........................................................164 Other Plants .........................................................171 Chromista...........................................................171 Fungi .............................................................173 Protozoans ..........................................................186 Non-native species 187 Vertebrates ..........................................................187 Invertebrates .........................................................187 Vascular Plants........................................................190 Extirpated species 207 Vertebrates ..........................................................207 Vascular Plants........................................................207 Change log 211 References 213 Index 215 3 Introduction Purpose to avoid implying -
Pacific Entomologist 1925-1966
RECOLLEcnONS OF A Pacific Entomologist 1925-1966 WITH PHOTOGRAPHS BY THE AUTHOR R.W. Paine Australian Centre for International Agricultural Research Canberra 1994 The Australian Centre for Intemational Agricultural Research (ACIAR) was established in June 1982 by an Act of Ihe Australian Parliament. lis primary mandate is 10 help identify agricultural problems in developing countries and to commission collaborative research between Australian and developing country researchers in fields where Australia has special competence. Where trade names ore used this does not constitute endorsement of nar discrimination against any product by the Centre. This peer-reviewed series contains the results of original research supported by ACIAR, or malerial deemed relevant 10 ACIAR's research and development objectives. The series is distributed intemationally, with an emphasis on developing countries. © Australian Centre for Intemational Agricultural Research GPO Box 157 t Conberra, Australia 2601 . Paine, R.w. 1994. Recollections of a Pacific Entomologist 1925 - 1966. ACIAR Monograph No 27. 120pp. ISBN 1 86320 106 8 Technical editing and production: Arowang Information Bureau Ply Ltd. Canberra Cover: BPD Graphic Associates, Canberra in association with Arawang Information Bureau Ply Lld Printed by The Craftsman Press Ply Ltd. Burwood, Victoria. ACIAR acknowledges the generous support of tihe Paine family in the compilation of this book. Long before agricultural 1920s was already at the Foreword sustainability entered forefront of world biological common parlance, or hazards control activities. Many of the associated with misuse of projects studied by Ron Paine pesticides captured headlines, and his colleagues are touched environmentally friendly on in his delightful and biological control of introduced evocative reminiscences. -
Additions, Deletions and Corrections to An
Bulletin of the Irish Biogeographical Society No. 36 (2012) ADDITIONS, DELETIONS AND CORRECTIONS TO AN ANNOTATED CHECKLIST OF THE IRISH BUTTERFLIES AND MOTHS (LEPIDOPTERA) WITH A CONCISE CHECKLIST OF IRISH SPECIES AND ELACHISTA BIATOMELLA (STAINTON, 1848) NEW TO IRELAND K. G. M. Bond1 and J. P. O’Connor2 1Department of Zoology and Animal Ecology, School of BEES, University College Cork, Distillery Fields, North Mall, Cork, Ireland. e-mail: <[email protected]> 2Emeritus Entomologist, National Museum of Ireland, Kildare Street, Dublin 2, Ireland. Abstract Additions, deletions and corrections are made to the Irish checklist of butterflies and moths (Lepidoptera). Elachista biatomella (Stainton, 1848) is added to the Irish list. The total number of confirmed Irish species of Lepidoptera now stands at 1480. Key words: Lepidoptera, additions, deletions, corrections, Irish list, Elachista biatomella Introduction Bond, Nash and O’Connor (2006) provided a checklist of the Irish Lepidoptera. Since its publication, many new discoveries have been made and are reported here. In addition, several deletions have been made. A concise and updated checklist is provided. The following abbreviations are used in the text: BM(NH) – The Natural History Museum, London; NMINH – National Museum of Ireland, Natural History, Dublin. The total number of confirmed Irish species now stands at 1480, an addition of 68 since Bond et al. (2006). Taxonomic arrangement As a result of recent systematic research, it has been necessary to replace the arrangement familiar to British and Irish Lepidopterists by the Fauna Europaea [FE] system used by Karsholt 60 Bulletin of the Irish Biogeographical Society No. 36 (2012) and Razowski, which is widely used in continental Europe. -
Japanese Pyraustinæ (Lepid.)
Title ON THE KNOWN AND UNRECORDED SPECIES OF THE JAPANESE PYRAUSTINÆ (LEPID.) Author(s) SHIBUYA, Jinshichi Citation Journal of the Faculty of Agriculture, Hokkaido Imperial University, 25(3), 151-242 Issue Date 1929-06-15 Doc URL http://hdl.handle.net/2115/12650 Type bulletin (article) File Information 25(3)_p151-242.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP ON THE KNOWN AND UNRECORDED SPECIES OF THE JAPANESE PYRAUSTINJE (LEPID.) BY JINSHICHI SHIBU¥A~ The object of this paper is to give a systematic account of the species belonging to the pyraustinae, a subfamily of ryralidae, Lepidoptera, which have hitherto been described from Japan, or recorded as occurring in this country. The preliminary account of the Pyraustinae of Japan was given by C. STOLL in his Papillons Exotiques, vol. iv, 1782, and in this publication he described a new species Phalaena (Pyralis) fascialis STOLL (=l£ymenia recurvalis FABR.). In 1860, MOTSCHULSKY in Etud. Entom. vol. ix, enu merated a new genus Nomis (= Udea), two new species Sylepta quadri maculalis, Udea albopedalis, the latter is the genotype of Nomis, and an unrecorded species Pyrausta sambucalis SCHIFF. et DEN. In regard to Sylepta quadrimaculalis MOTSCH., this species was originally placed under genus Botyodes, and with its specific name Sylepta quadrimaculalis was already given by KOLLER for a Pyralid-moth in 1844, while G. F. HAMPSON elected a new name Sylepta inferior H~IPSN. for S. quadrimaculalis MOTSCH. In 1863, LEDERER in Wien. Ent. Mon. vii, recorded Margaronia perspectalz's 1 \VLK. from this country as Phace!lura advenalz's LED. -
Heteroptera: Hemiptera ) from Chhattisgarh, India
BISWAS et al.: On an account of Pentatomoidea.....from Chhattisgarh, India ISSN 0375-1511211 Rec. zool. Surv. India : 114(Part-2) : 211-231, 2014 ON AN ACCOUNT OF PENTATOMOIDEA (HETEROPTERA: HEMIPTERA ) FROM CHHATTISGARH, INDIA B. BISWAS, M. E. HASSAN, KAILASH CHANDRA, SANDEEP KUSHWAHA** AND PARAMITA MUKHERJEE Zoological Survey of India, M-Block, New Alipore, Kolkata-700053, India ** Zoological Survey of India, Central Zone Regional Centre, Vijay Nagar, Jabalpur-482002 INTRODUCTION SYSTEMATIC ACCOUNT The pentatomids are commonly known as Family I PENTATOMIDAE “shield bugs” or “stink bugs” as their bodies are Subfamily PENTATOMINAE usually covered by a shield shaped scutellum covering more than half of the abdomen, tibia with Tribe ANTESTINI weak or no spine, 5 segmented antennae which Genus 1. Antestia Stal, 1864 gives its family name and most of them emit an 1. Antestia anchora (Thunberg) unpleasant odour, offensive in nature, produced by a pair of glands in the thorax and is released through *2. Antestia cruciata (Fabricius) openings in the metathorax. Although majority Genus 2. Plautia Stal, 1867 of these bugs are plant sucking, the members *3. Plautia crossota (Fabricius) belonging to the family Asopinae are wholly or partially predaceous. Pentatomoidea is one of the Tribe AGONOSCELIDINI largest superfamilies of Heteroptera comprising of Genus 3. Agonoscelis Spin, 1837 1301 genera and 7182 species distributed in sixteen 4. Agonoscelis nubilis (Fabricius) families all over the world (Henry, 2009). Of these, family Pentatomidae alone represents 896 genera Tribe CARPOCORINI and 4722 species distributed in eight subfamilies Genus 4. Gulielmus Distant, 1901 (Pentatominae, Asopinae, Podopinae, Edessinae, 5. Gulielmus laterarius Distant Phyllocephalinae, Discocephalinae, Cyrtocorinae and Serbaninae). -
Insect & Mite Management
BANANAS INSECT & MITE MANAGEMENT Bruno Pinese Queensland Fruit &. Vegetable Growers Richard Piper BANANAS INSECT & MITE MANAGEMENT Bruno Pinese Richard Piper DEPARTMENT OF PRIMARY INDUSTRIES QUEENSLAND ISSN 0727-6273 Agdex 231/620 First published 1994 National Library of Australia Cataloguing-in-Publication data: Pinese, B. (Bruno), 1949-. Bananas: insect and mite management. ISBN 0 7242 5401 3. 1. Banana- Diseases and pests- Control- Queensland. I. Piper, Richard, 1958-. II. Queensland. Dept. of Primary Industries. Ill. Title. (Series: Information series (Queensland. Dept. of Primary Industries); QI93048). 634.77299 Editing, production and printing managed by Publishing Services ©Queensland Government 1994 Department of Primary Industries GPO Box46 Brisbane Q 4001 Cover: Stethorus larva: bunch of Cavendish bananas within a protective polythene sleeve CONTENTS Foreword v Acknowledgements vi About the authors vii Preface IX Notes to growers X 1 THE INTEGRA TED PEST MANAGEMENT (I PM) CONCEPT 2 BIOLOGICAL CONTROL OF BANANA PESTS 3 3 MONITORING PROCEDURES 5 4 MAJOR PESTS 9 Banana scab moth (Nacoleia octasema) 9 Banana rust thrips (Chaetanaphothrips signipennis) 13 Mites: Banana spider mite (Tetranychus lambi) 17 Two-spolled mite (Terranychus urticae) 17 Biological control: M ite-eating ladybird (Stethoms) 2 1 Banana weevil borer (Cosmopolites sordidus) 23 Sugarcane bud moth (Opogona glycyphaga) 26 Banana fl ower Lhrips (Thrips hawaiiensis) 28 5 MINOR PESTS 31 Banana aphid ( Pentalonia nigronervosa) 3 1 Red houldered leaf beetle (Monolepta -
Four Newly Recorded Species of the Family Crambidae (Lepidoptera) from Korea
Anim. Syst. Evol. Divers. Vol. 30, No. 4: 267-273, October 2014 http://dx.doi.org/10.5635/ASED.2014.30.4.267 Short communication Four Newly Recorded Species of the Family Crambidae (Lepidoptera) from Korea Seung Jin Roh1, Sung-Soo Kim2, Yang-Seop Bae3, Bong-Kyu Byun1,* 1Department of Biological Science & Biotechnology, Hannam University, Daejeon 305-811, Korea 2Research Institute for East Asian Environment and Biology, Seoul 134-852, Korea 3Division of Life Sciences, Incheon National University, Incheon 406-772, Korea ABSTRACT This study was carried out to report the newly recorded species of the family Crambidae, belonging to the order Lepidoptera. During the course of investigation on the family Crambidae in South Korea, the following four species are reported for the first time from Korea: Diplopseustis perieresalis (Walker, 1859), Dolichar- thria bruguieralis (Duponchel, 1833), Herpetogramma ochrimaculale (South, 1901), and Omiodes diemenalis (Guenée, 1854). Among them two genera, Diplopseustis Meyrick and Dolicharthria Stephens, are also newly reported from Korea. External and genital characteristics of adults were examined and illustrated. All of the newly recorded species were enumerated with their available information including the collecting localities, illustrations of adults, and genitalia. Keywords: Lepidoptera, Crambidae, new record, Korea INTRODUCTION MATERIALS AND METHODS Until now, more than 16,000 species of the superfamily Pyra- Materials examined in the present study are preserved in the lodiea have been recorded in the world (Munroe and Solis, Systematic Entomology Laboratory, Hannam University 1999). In Korea, a total of 349 species of the superfamily (SELHNU), Daejeon, Korea. The genitalia of both sexes were Pyralodiea have been known to date (Bae et al., 2008). -
Michael Fibiger 1945 - 2011
Esperiana Band 16: 7-38 Schwanfeld, 06. Dezember 2011 ISBN 978-3-938249-01-7 Michael FIBIGER 1945 - 2011 Our dear friend and colleague, Michael FIBIGER, died on 16 February, 2011, peacefully and in the presence of the closest members of his family. For close on 18 months he had battled heroically and with characteristic determination against a particularly unpleasant form of cancer, and continued with his writing and research until close to the end. Michael was born on 29 June, 1945, in Hellerup, a suburb of Copenhagen, and began catching moths at the age of nine, particularly in the vicinity of the summer house where they stayed on the north coast of Zealand. By the time he was 11, he wanted to join the Danish Lepidoptera Society but was told he was too young and must wait “a couple of years”. So, exactly two years later he applied again and was accepted – as the youngest-ever Member of the Society. Michael always knew he wanted to be a teacher, and between 1965 and 1970 he attended training college at Hel- lerup Seminarium. Having graduated, he taught Danish, Biology and Special Education at Gentofte School until 1973. In the meantime, he studied Clinical Psychology at the University of Copenhagen from 1970 to 1976, and from 1973 to 1981 he became School Psychologist for elementary schools and high schools in the municipality of Gentofte, work which involved investigation and testing of children with psychiatric problems, counselling, supervi- sion and therapy. He was also an instructor in drug prevention for the Ministry of Education.