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Survey of Predatory Coccinellids (Coleoptera
Survey of Predatory Coccinellids (Coleoptera: Coccinellidae) in the Chitral District, Pakistan Author(s): Inamullah Khan, Sadrud Din, Said Khan Khalil and Muhammad Ather Rafi Source: Journal of Insect Science, 7(7):1-6. 2007. Published By: Entomological Society of America DOI: http://dx.doi.org/10.1673/031.007.0701 URL: http://www.bioone.org/doi/full/10.1673/031.007.0701 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. Journal of Insect Science | www.insectscience.org ISSN: 1536-2442 Survey of predatory Coccinellids (Coleoptera: Coccinellidae) in the Chitral District, Pakistan Inamullah Khan, Sadrud Din, Said Khan Khalil and Muhammad Ather Rafi1 Department of Plant Protection, NWFP Agricultural University, Peshawar, Pakistan 1 National Agricultural Research Council, Islamabad, Pakistan Abstract An extensive survey of predatory Coccinellid beetles (Coleoptera: Coccinellidae) was conducted in the Chitral District, Pakistan, over a period of 7 months (April through October, 2001). -
Genetically Modified Baculoviruses for Pest
INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS This page intentionally left blank INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS EDITED BY LAWRENCE I. GILBERT SARJEET S. GILL Amsterdam • Boston • Heidelberg • London • New York • Oxford Paris • San Diego • San Francisco • Singapore • Sydney • Tokyo Academic Press is an imprint of Elsevier Academic Press, 32 Jamestown Road, London, NW1 7BU, UK 30 Corporate Drive, Suite 400, Burlington, MA 01803, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA ª 2010 Elsevier B.V. All rights reserved The chapters first appeared in Comprehensive Molecular Insect Science, edited by Lawrence I. Gilbert, Kostas Iatrou, and Sarjeet S. Gill (Elsevier, B.V. 2005). All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publishers. Permissions may be sought directly from Elsevier’s Rights Department in Oxford, UK: phone (þ44) 1865 843830, fax (þ44) 1865 853333, e-mail [email protected]. Requests may also be completed on-line via the homepage (http://www.elsevier.com/locate/permissions). Library of Congress Cataloging-in-Publication Data Insect control : biological and synthetic agents / editors-in-chief: Lawrence I. Gilbert, Sarjeet S. Gill. – 1st ed. p. cm. Includes bibliographical references and index. ISBN 978-0-12-381449-4 (alk. paper) 1. Insect pests–Control. 2. Insecticides. I. Gilbert, Lawrence I. (Lawrence Irwin), 1929- II. Gill, Sarjeet S. SB931.I42 2010 632’.7–dc22 2010010547 A catalogue record for this book is available from the British Library ISBN 978-0-12-381449-4 Cover Images: (Top Left) Important pest insect targeted by neonicotinoid insecticides: Sweet-potato whitefly, Bemisia tabaci; (Top Right) Control (bottom) and tebufenozide intoxicated by ingestion (top) larvae of the white tussock moth, from Chapter 4; (Bottom) Mode of action of Cry1A toxins, from Addendum A7. -
COLEOPTERA COCCINELLIDAE) INTRODUCTIONS and ESTABLISHMENTS in HAWAII: 1885 to 2015
AN ANNOTATED CHECKLIST OF THE COCCINELLID (COLEOPTERA COCCINELLIDAE) INTRODUCTIONS AND ESTABLISHMENTS IN HAWAII: 1885 to 2015 JOHN R. LEEPER PO Box 13086 Las Cruces, NM USA, 88013 [email protected] [1] Abstract. Blackburn & Sharp (1885: 146 & 147) described the first coccinellids found in Hawaii. The first documented introduction and successful establishment was of Rodolia cardinalis from Australia in 1890 (Swezey, 1923b: 300). This paper documents 167 coccinellid species as having been introduced to the Hawaiian Islands with forty-six (46) species considered established based on unpublished Hawaii State Department of Agriculture records and literature published in Hawaii. The paper also provides nomenclatural and taxonomic changes that have occurred in the Hawaiian records through time. INTRODUCTION The Coccinellidae comprise a large family in the Coleoptera with about 490 genera and 4200 species (Sasaji, 1971). The majority of coccinellid species introduced into Hawaii are predacious on insects and/or mites. Exceptions to this are two mycophagous coccinellids, Calvia decimguttata (Linnaeus) and Psyllobora vigintimaculata (Say). Of these, only P. vigintimaculata (Say) appears to be established, see discussion associated with that species’ listing. The members of the phytophagous subfamily Epilachninae are pests themselves and, to date, are not known to be established in Hawaii. None of the Coccinellidae in Hawaii are thought to be either endemic or indigenous. All have been either accidentally or purposely introduced. Three species, Scymnus discendens (= Diomus debilis LeConte), Scymnus ocellatus (=Scymnobius galapagoensis (Waterhouse)) and Scymnus vividus (= Scymnus (Pullus) loewii Mulsant) were described by Sharp (Blackburn & Sharp, 1885: 146 & 147) from specimens collected in the islands. There are, however, no records of introduction for these species prior to Sharp’s descriptions. -
Taxonomic Redescription of the Species of Sub- Family Chilocorinae
International Journal of Chemical Studies 2018; 6(6): 1465-1469 P-ISSN: 2349–8528 E-ISSN: 2321–4902 IJCS 2018; 6(6): 1465-1469 Taxonomic redescription of the species of sub- © 2018 IJCS Received: 26-09-2018 family Chilocorinae (Coleoptera: Coccinellidae) Accepted: 30-10-2018 from Jammu and Kashmir, India Ajaz Ahmad Kundoo Division of Entomology, Sher-e-Kashmir University of Ajaz Ahmad Kundoo, Akhtar Ali Khan, Ishtiyaq Ahad, NA Bhat, MA Agricultural Sciences and Chatoo and Khalid Rasool Technology of Kashmir, Wadura Campus, Baramullah, Jammu and Kashmir, India Abstract Ladybugs are diverse group of living organisms. They belong to family Coccinellidae of order Akhtar Ali Khan Coleoptera. The family has been subdivided into six subfamilies: Sticholotidinae, Chilochorinae, Division of Entomology, Scymninae, Coccidulinae, Coccinellinae and Epilachninae. These are universal predators and occupy Sher-e-Kashmir University of important place in biological control. In this paper four species of the subfamily Chilocorinae have been Agricultural Sciences and collected and rediscribed as no taxonomic work has been done on this group in Kashmir, India. This Technology of Kashmir, paper provides a detailed taxonomy of Chilocorus infernalis, Chilocorus rubidus, Pricibrumus Shalimar Campus, Jammu and uropygialis and Platynaspidius saundersi on the basis of advanced taxonomic character that is male Kashmir, India genitalia. Detailed description of adults, male genitalia and taxonomic keys are provided for each species Ishtiyaq Ahad along with color plates. Division of Entomology, Sher-e-Kashmir University of Keywords: Chilocorinae, Kashmir, male genitalia, taxonomy, taxonomic keys. Agricultural Sciences and Technology of Kashmir, Wadura Introduction Campus, Baramullah, Jammu Coccinellids are commonly known as ladybird beetles. -
Coleoptera: Coccinellidae): Influence of Subelytral Ultrastructure
Experimental & Applied Acarology, 23 (1999) 97–118 Review Phoresy by Hemisarcoptes (Acari: Hemisarcoptidae) on Chilocorus (Coleoptera: Coccinellidae): influence of subelytral ultrastructure M.A. Houck* Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409–3131, USA (Received 9 January 1997; accepted 17 April 1998) ABSTRACT The non-phoretic stages of mites of the genus Hemisarcoptes are predators of the family Diaspididae. The heteromorphic deutonymph (hypopus) maintains a stenoxenic relationship with beetles of the genus Chilocorus. The mites attach to the subelytral surface of the beetle elytron during transport. There is variation in mite density among species of Chilocorus. Both Hemisarcoptes and Chilocorus have been applied to biological control programmes around the world. The objective of this study was to determine whether subelytral ultrastructure (spine density) plays a role in the evolution of symbiosis between the mite and the beetle. The subelytral surfaces of 19 species of Chilocorus and 16 species of Exochomus were examined. Spine density was determined for five subelytral zones: the anterior pronotal margin, medial central region, caudoventral tip, lateral distal margin and epipleural region. Spine density on the subelytral surface of Chilocorus and Exochomus was inversely correlated with the size of the elytron for all zones except the caudoventral tip. This suggests that an increase in body size resulted in a redistribution of spines and not an addition of spines. The pattern of spine density in Exochomus and Chilocorus follows a single size–density trajectory. The pattern of subelytral ultrastructure is not strictly consistent with either beetle phylogeny or beetle allometry. The absence of spines is not correlated with either beetle genus or size and species of either Chilocorus or Exochomus may be devoid of spines in any zone, irrespective of body size. -
(Malus Domostica Borkhis) One of the -..::Egyptian Journal of Plant
Egypt. J. Plant Prot. Res. Inst. (2020), 3 (4): 1218-1240 Egyptian Journal of Plant Protection Research Institute www.ejppri.eg.net Survey and population dynamics of scale insects (Hemiptera :Coccoidea) infesting apple trees and thier natural enemies in Egypt EL-Amir, S. M.; Yomna, N. M. Abd Allah; Mona, Moustafa and Shaaban, Abd-Rabou Plant Protection Research Institute, Agricultural Research Center, Dokki, Giza, Egypt. ARTICLE INFO Abstract : Article History Apple (Malus domostica Borkhis) one of the most important Received: 5/ 10 /2020 deciduous fruit trees in Egypt. Scale insects (Hemiptera : Coccoidea) Accepted: 24/11 /2020 are the most important pests infested orchard trees including apple . The present work dealt with the survey of scale insects infested apple trees and their natural enemies in different locations in Egypt as well Keywords as population dynamics of the dominant species infested apple of Apple trees, survey , these pests. The results indicated that 21 species of scale insects were population dynamics , recorded infested apple trees in Egypt. The dominant species were scale insects , natural Hemiberlesia lataniae (Signoret), Lepidosaphes beckii (Newman) , enemies and Egypt. Lepidosaphes pallidula (Williams), Parlatoria oleae (Colvée) ((Hemiptera :Coccoidea: Diaspididae) , Planococcus citri (Risso), Planococcus ficus (Signoret) (Hemiptera :Coccoidea: Pseudococcidae) and Russellaspis pustulans pustulans (Cockerell) (Hemiptera :Coccoidea: Asterolecaniidae). Also, in the present work 19 parasitoids and 2 hyperparasitiods and 33 predators were recorded associated with scale insects infesting apple trees. The dominant species were, the parasitoids Aphytis chrysomphali (Mercet), Aphytis maculicornis (Masi), Aphytis lepidosaphes Compere, Encarsia citrina (Craw) (Hymenoptera: Aphelinidae), Leptomastidea abnormis (Girault) , Metaphycus asterolecanii (Mercet) and Zaplatycerus kemticus (Trjapitzin and Triapitsyn) (Hymenoptera : Encyrtidae) and the predators Chilocorus bipustulatus L. -
Crapemyrtle Bark Scale Acanthococcus Lagerstroemiae Kuwana (Hemiptera: Eriococcidae): Analysis of Factors Influencing Infestation and Control
CRAPEMYRTLE BARK SCALE ACANTHOCOCCUS LAGERSTROEMIAE KUWANA (HEMIPTERA: ERIOCOCCIDAE): ANALYSIS OF FACTORS INFLUENCING INFESTATION AND CONTROL A Thesis by KYLE ANDREW GILDER Submitted to the Office of Graduate and Professional Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE Chair of Committee, Kevin M. Heinz Co-Chair of Committee, Mengmeng Gu Committee Members, Mike Merchant Head of Department, Phillip Kaufman December 2020 Major Subject: Entomology Copyright 2020 Kyle Andrew Gilder ABSTRACT Crapemyrtle bark scale, Acanthococcus lagerstroemiae (Kuwana), a new non-native pest from Asia first discovered in the U.S. in 2004 has now been reported in 14 states. The scale jeopardizes the future of crapemyrtles use as a popular ornamental landscape tree in the U.S. Management of this pest will likely include biological strategies. Before such strategies can be implemented it is important to examine relative abundances and distributions of arthropod species associated with the scale in the geographic area targeted for biological control. In the first objective, surveys of crapemyrtle ecology from two varietal groups of crapemyrtle trees (Lagerstroemia spp.) were undertaken in Tarrant and Brazos counties across six consecutive seasons in 2018 – 2019. A rich arthropod community was discovered. The most common predators were spiders, coccinellids, and chrysopids. Insects in the families Eriococcidae, Aphididae, and Thripidae were common herbivores on Lagerstroemia spp. Numerous phytophagous and mycophagous mites were also collected. These herbivores constitute a reservoir of alternative prey for generalist predators that may also feed on A. lagerstroemiae. A food web was constructed to illustrate direct and indirect effects of the predator community on A. -
Chilocorus Czrcumdatus Gyllenhal Newly Established in Australia and Additional Records for Coccinella Undecimpuncta Ta L
J. Aust. ent. SOC., 1991, 30: 341-342 341 CHILOCORUS CZRCUMDATUS GYLLENHAL NEWLY ESTABLISHED IN AUSTRALIA AND ADDITIONAL RECORDS FOR COCCINELLA UNDECIMPUNCTA TA L. (COLEOPTERA: COCCINELLIDAE) K. J. HOUSTON' Department of Primary Industries, Meiers Road, Indooroopilly, Qld 4068. Abstract Chilocorus circumdatus Gyllenhal is recorded as established in Australia for the first time with Unaspis citri (Comstock) and Aspidiotus nerii Bouche (Hemiptera: Diaspididae) as new prey records. Additional distributional records are given for Coccinella undecimpunctata. Abbreviations: ANIC, Australian National Insect Collection, CSIRO, Canberra: IPS, Institute of Plant Sciences, Burnley; QDPI, Queensland Department of Primary Industries, Brisbane; WADA, Western Australia Department of Agriculture, South Perth. Chilocorus circumdatus Gyllenhal Material eXUmined-QUEENSLAND: 1 6,3 55, Charters Towers, 13.vi.1990, J. D. Brown, on citrus (QDPI) [eating Unuspis citri (Comstock), J. D. Brown and D. Smith pers. comm.]; CHINA:1 6,1 ?, scale feeder (WADA); 1 6, scale feeder, Aspidiotus (WADA); 1 0,Zhan Jiang, l.xi.1988, G. K. Waite, on citrus (QDPI); INDIA:3 66,5 ??, Bangalore, 1 i.1960 (WADA). The specimens from Queensland agree with those from China and India in punctation and morphology. This species is recognisable by its dorsal colour pattern, yellow with thin black external margins of the elytra. (Pang and Mao 1979, Plate VII, Fig. 67). In addition, the male and female genitalia agree with those illustrated in Miyatake (1970, Figs 39-43), Nagaraja and Hussainy (1967, Figs 2, 2a, 8, 20, 30) and Pang and Mao (1979, Fig. 79). The siphonal apex is membranous, similar to that shown in Miyatake (1970, Fig. 41) [the membranous apex is also shown in Pang and Mao (1979) but not in Nagaraja and Hussainy (1967)l. -
Temperature-Dependent Development of Chilocorus
Türk. entomol. derg., 2013, 37 (2): 185-194 ISSN 1010-6960 Orijinal araştırma (Original article) Temperature-dependent development of Chilocorus bipustulatus (L.) (Coleoptera: Coccinellidae) on Aspidiotus nerii Bouché (Hemiptera: 1 Diaspididae) under laboratory conditions Aspidiotus nerii Bouché (Hemiptera: Diaspididae) ile beslenen Chilocorus bipustulatus (L.) (Coleoptera: Coccinellidae)’un laboratuvar koşullarında sıcaklığa bağlı gelişmesi 2 3* Zennure SATICI KARATAY İsmail KARACA Summary Chilocorus bipustulatus (L.) is an important predator of scale insects that is widely distributed in citrus plantations in the Mediterranean Region of Turkey. The developmental time of C. bipustulatus, a polyphagous predator, was studied at six different, constant temperatures (14, 18, 22, 26, 30 and 34°C) and a relative humidity (R.H. of 65±1%, with Aspidiotus nerii Bouché (Hemiptera: Diaspididae) as the prey. The developmental periods of immature stages were 61.67, 51.00, 41.21, 33.72, 26.76 and 27.17 days at 14, 18, 22, 26, 30 and 34 °C, respectively. The developmental threshold for C. bipustulatus determined with the linear model was 5.91. Linear regression was employed to determine the thermal constant of 651.1 degree-days.In this study linear and nonlinear regression models are discussed. Key words: Temperature dependent development, linear model, nonlinear model, Chilocorus bipustulatus Özet Chilocorus bipustulatus (L.) (Coleoptera: Coccinellidae) Akdeniz Bölgesinde (Türkiye) turunçgil alanlarında yaygın olarak bulunan önemli bir kabuklubit avcısıdır. Aspidiotus nerii Bouché (Hemiptera: Diaspididae) üzerinde beslenen C. bipustulatus‘un, nemi % 65±1’e ayarlı iklim dolaplarında 6 farklı sabit sıcaklıkta (14, 18, 22, 26, 30 ve 34°C) sıcaklığa bağlı gelişme süreleri incelenmiştir. Avcının ergin öncesi gelişme süreleri 14, 18, 22, 26, 30 ve 34°C sıcaklıklarda sırasıyla 61.67, 51.00, 41.21, 33.72, 26.76 ve 27.17 gün sürmüştür. -
The Role of Ecological Compensation Areas in Conservation Biological Control
The role of ecological compensation areas in conservation biological control ______________________________ Promotor: Prof.dr. J.C. van Lenteren Hoogleraar in de Entomologie Promotiecommissie: Prof.dr.ir. A.H.C. van Bruggen Wageningen Universiteit Prof.dr. G.R. de Snoo Wageningen Universiteit Prof.dr. H.J.P. Eijsackers Vrije Universiteit Amsterdam Prof.dr. N. Isidoro Università Politecnica delle Marche, Ancona, Italië Dit onderzoek is uitgevoerd binnen de onderzoekschool Production Ecology and Resource Conservation Giovanni Burgio The role of ecological compensation areas in conservation biological control ______________________________ Proefschrift ter verkrijging van de graad van doctor op gezag van de rector magnificus van Wageningen Universiteit, Prof. dr. M.J. Kropff, in het openbaar te verdedigen op maandag 3 september 2007 des namiddags te 13.30 in de Aula Burgio, Giovanni (2007) The role of ecological compensation areas in conservation biological control ISBN: 978-90-8504-698-1 to Giorgio Multaque tum interiisse animantum saecla necessest nec potuisse propagando procudere prolem. nam quaecumque vides vesci vitalibus auris aut dolus aut virtus aut denique mobilitas est ex ineunte aevo genus id tutata reservans. multaque sunt, nobis ex utilitate sua quae commendata manent, tutelae tradita nostrae. principio genus acre leonum saevaque saecla tutatast virus, vulpis dolus et gfuga cervos. at levisomma canum fido cum pectore corda et genus omne quod est veterino semine partum lanigeraeque simul pecudes et bucera saecla omnia sunt hominum tutelae tradita, Memmi. nam cupide fugere feras pacemque secuta sunt et larga suo sine pabula parta labore, quae damus utilitatiseorum praemia causa. at quis nil horum tribuit natura, nec ipsa sponte sua possent ut vivere nec dare nobis praesidio nostro pasci genus esseque tatum, scilicet haec aliis praedae lucroque iacebant indupedita suis fatalibus omnia vinclis, donec ad interutum genus id natura redegit. -
(Coleoptera; Coccinellidae), from a MITE, Hemisarcoptes Cooremani
THE UPTAKE OF TRITIATED WATER BY A BEETLE, Chilocorus cacti (Coleoptera; Coccinellidae), FROM A MITE, Hemisarcoptes cooremani (Acari: Acariformes) by AURAL! E. HOLTE, B.S. A THESIS IN BIOLOGY Submitted to the Graduate Faculty of Texas Tech University in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Approved December, 1999 mr'-^'^-"""'^'" .——^—--— •« • "ji» • »j»«p»^"^i^»w /^n^^l C>^i^f ACKNOWLEDGMENTS I thank a number of people for their assistance and support in the completion of iS-f' 7^ this work. First, I would like to thank Dr. Marilyn Houck for her generous encouragement, understanding and guidance, without which I would not have been able to start or complete this project. I also thank the members of my committee. Dr. Nathan Collie and Dr. Richard Deslippe who provided valuable comments and information utilized for this research. Elizabeth Richards, Heather Roberts, and Qingtian Li were encouraging and helpful colleagues in all my endeavors as a graduate student. I also thank a number of people for personal support; foremost, Damon for without his devoted love, constant support and immutable encouragement, I would have not been able to accomplish this work. I v^sh to thank my family for all of the love and understanding they have given me, especially my mother who guided me with her example, demonstrating that I could do anything once I set my mind to it. I also would like to acknowledge all of the other friends and family members who have given me encouragement. Finally, financial support for this research was provided by the Texas Tech University Biology Department and the Bi-National Agricultural Research and Development grants (#IS-1397-87 and #US-2359-93C to M. -
Harmonia Axyridis in Britain
Modelling the impact of an alien invasion: Harmonia axyridis in Britain Richard Francis Comont Linacre College Trinity term 2013 A thesis submitted for the degree of Doctor of Philosophy Word count: 31,043 i Contents Summary ........................................................................................................................................... vi Declaration ....................................................................................................................................... vii Dedication and Acknowledgements .............................................................................................viii Chapter 1. General introduction ......................................................................................... 1 1. 1.1. Defining alien species and invasive alien species ....................................................... 1 1. 1.2. Impacts and costs of Invasive Alien Species ............................................................... 1 1. 1.3. Trends in arrival, establishment and spread of IAS ..................................................... 2 1. 1.4. Pathways of introduction and spread – how do IAS arrive? ...................................... 3 1. 1.5. From alien to invasive ...................................................................................................... 4 1. 1.6. From alien to invasive – the traits of invasive species ................................................ 5 1. 1.7. Invasibility of native communities – the diversity-invasibility hypothesis