Developing Host Range Testing for Cotesia Urabae
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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. -
Common Pathways by Which Non-Native Forest Insects Move
Journal of Pest Science (2019) 92:13–27 https://doi.org/10.1007/s10340-018-0990-0 REVIEW Common pathways by which non‑native forest insects move internationally and domestically Nicolas Meurisse1 · Davide Rassati2 · Brett P. Hurley3 · Eckehard G. Brockerhof4 · Robert A. Haack5 Received: 18 February 2018 / Revised: 29 April 2018 / Accepted: 12 May 2018 / Published online: 30 May 2018 © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract International trade and movement of people are largely responsible for increasing numbers of non-native insect introductions to new environments. For forest insects, trade in live plants and transport of wood packaging material (WPM) are considered the most important pathways facilitating long-distance invasions. These two pathways as well as trade in frewood, logs, and processed wood are commonly associated with insect infestations, while “hitchhiking” insects can be moved on cargo, in the conveyances used for transport (e.g., containers, ships), or associated with international movement of passengers and mail. Once established in a new country, insects can spread domestically through all of the above pathways. Considerable national and international eforts have been made in recent years to reduce the risk of international movement of plant pests. International Standards for Phytosanitary Measures (ISPMs) No. 15 (WPM), 36 (plants for planting), and 39 (wood) are examples of phytosanitary standards that have been adopted by the International Plant Protection Convention to reduce risks of invasions of forest pests. The implementation of ISPMs by exporting countries is expected to reduce the arrival rate and establishments of new forest pests. However, many challenges remain to reduce pest transportation through international trade, given the ever-increasing volume of traded goods, variations in quarantine procedures between countries, and rapid changes in distribution networks. -
Protection of Pandora Moth (Coloradia Pandora Blake) Eggs from Consumption by Golden-Mantled Ground Squirrels (Spermophilus Lateralis Say)
AN ABSTRACT OF THE THESIS OF Elizabeth Ann Gerson for the degree of Master of Science in Forest Science presented on 10 January, 1995. Title: Protection of Pandora Moth (Coloradia pandora Blake) Eggs From Consumption by Golden-mantled Ground Squirrels (Spermophilus lateralis Say) Abstract approved: Redacted for Privacy William C. McComb Endemic populations of pandora moths (Coloradia pandora Blake), a defoliator of western pine forests, proliferated to epidemic levels in central Oregon in 1986 and increased dramatically through 1994. Golden-mantled ground squirrels (Spermophilus lateralis Say) consume adult pandora moths, but reject nutritionally valuable eggs from gravid females. Feeding trials with captive S. lateralis were conducted to identify the mode of egg protection. Chemical constituents of fertilized eggs were separated through a polarity gradient of solvent extractions. Consumption of the resulting hexane, dichloromethane, and water egg fractions, and the extracted egg tissue residue, was evaluated by randomized 2-choice feeding tests. Consumption of four physically distinct egg fractions (whole eggs, "whole" egg shells, ground egg shells, and egg contents) also was evaluated. These bioassays indicated that C. pandora eggs are not protected chemically, however, the egg shell does inhibit S. lateralis consumption. Egg protection is one mechanism that enables C. pandora to persist within the forest food web. Spermophilus lateralis, a common and often abundant rodent of central Oregon pine forests, is a natural enemy of C. pandora -
The Painted Apple Moth Eradication Programme (B)
CASE PROGRAM 2006-10.2 The Painted Apple Moth Eradication Programme (B) In late August 2002, Murray Sherwin, Director-General of the New Zealand Ministry of Agriculture and Forestry (MAF) had to decide whether to reverse his department’s recommendation, made to Cabinet barely a month before, for the future management of the Painted Apple Moth (PAM) incursion. The fast-breeding moth, discovered three years earlier, threatened New Zealand’s plantation forests as well as its native bush, potentially robbing the economy of $356 million in exports. Despite eradication efforts, including the controversial use of aerial sprays, new areas of infestation were still being discovered. Murray Sherwin had become chief executive less than a year ago, arriving at MAF as controversy was building around his Forest Biosecurity Group’s management of PAM. MAF’s recommendation to Cabinet in July 2002, based on the weight of internal and external advice, and concern about the $90 million estimated cost of an all-out eradication attempt, was to continue with containment activities while further investigating other means of managing the pest. Government’s response was to allocate $11 million in immediate resources and call for more detailed information on the options of long-term management, or a renewed attempt at full eradication. Sherwin realised there was substantial political support, despite the odds, for eradication. He now needed to know whether his department, besieged by media and community criticism, could believe in and commit to the task. This case was developed by the Australia and New Zealand School of Government (ANZSOG) and funded by the New Zealand Ministry of Agriculture and Forestry (MAF). -
Trees for Farm Forestry: 22 Promising Species
Forestry and Forest Products Natural Heritage Trust Helping Communities Helping Australia TREES FOR FARM FORESTRY: 22 PROMISING SPECIES Forestry and Forest Products TREES FOR FARM FORESTRY: Natural Heritage 22 PROMISING SPECIES Trust Helping Communities Helping Australia A report for the RIRDC/ Land & Water Australia/ FWPRDC Joint Venture Agroforestry Program Revised and Edited by Bronwyn Clarke, Ian McLeod and Tim Vercoe March 2009 i © 2008 Rural Industries Research and Development Corporation. All rights reserved. ISBN 1 74151 821 0 ISSN 1440-6845 Trees for Farm Forestry: 22 promising species Publication No. 09/015 Project No. CSF-56A The information contained in this publication is intended for general use to assist public knowledge and discussion and to help improve the development of sustainable regions. You must not rely on any information contained in this publication without taking specialist advice relevant to your particular circumstances. While reasonable care has been taken in preparing this publication to ensure that information is true and correct, the Commonwealth of Australia gives no assurance as to the accuracy of any information in this publication. The Commonwealth of Australia, the Rural Industries Research and Development Corporation (RIRDC), the authors or contributors expressly disclaim, to the maximum extent permitted by law, all responsibility and liability to any person, arising directly or indirectly from any act or omission, or for any consequences of any such act or omission, made in reliance on the contents of this publication, whether or not caused by any negligence on the part of the Commonwealth of Australia, RIRDC, the authors or contributors. The Commonwealth of Australia does not necessarily endorse the views in this publication. -
Crop Colonization by Pests and Specialist Enemies
insects Article Dispersal in Host–Parasitoid Interactions: Crop Colonization by Pests and Specialist Enemies Edward W. Evans Department of Biology, Utah State University, Logan, UT 84322-5305, USA; [email protected]; Tel.: +01-435-797-2552 Received: 7 September 2018; Accepted: 2 October 2018; Published: 5 October 2018 Abstract: Interactions of insect pests and their natural enemies increasingly are being considered from a metapopulation perspective, with focus on movements of individuals among habitat patches (e.g., individual crop fields). Biological control may be undercut in short-lived crops as natural enemies lag behind the pests in colonizing newly created habitat. This hypothesis was tested by assessing parasitism of cereal leaf beetle (Oulema melanopus) and alfalfa weevil (Hypera postica) larvae at varying distances along transects into newly planted fields of small grains and alfalfa in northern Utah. The rate of parasitism of cereal leaf beetles and alfalfa weevils by their host-specific parasitoids (Tetrastichus julis (Eulophidae) and Bathyplectes curculionis (Ichneumonidae), respectively) was determined for earliest maturing first generation host larvae. Rates of parasitism did not vary significantly with increasing distance into a newly planted field (up to 250–700 m in individual experiments) from the nearest source field from which pest and parasitoid adults may have immigrated. These results indicate strong, rapid dispersal of the parasitoids in pursuing their prey into new habitat. Thus, across the fragmented agricultural landscape of northern Utah, neither the cereal leaf beetle nor the alfalfa weevil initially gained substantial spatial refuge from parasitism by more strongly dispersing than their natural enemies into newly created habitat. -
Hymenoptera: Braconidae), Parasitoids of Gramineous Stemborers in Africa
Eur. J. Entomol. 107: 169–176, 2010 http://www.eje.cz/scripts/viewabstract.php?abstract=1524 ISSN 1210-5759 (print), 1802-8829 (online) Host recognition and acceptance behaviour in Cotesia sesamiae and C. flavipes (Hymenoptera: Braconidae), parasitoids of gramineous stemborers in Africa MESHACK OBONYO1, 2, FRITZ SCHULTHESS3, BRUNO LE RU 2, JOHNNIE VAN DEN BERG1 and PAUL-ANDRÉ CALATAYUD2* 1School of Environmental Science and Development, North-West University, Potchefstroom, 2520, South Africa 2Institut de Recherche pour le Développement (IRD), UR 072, c/o International Centre of Insect Physiology and Ecology ( ICIPE), Noctuid Stemborer Biodiversity (NSBB) Project, PO Box 30772-00100, Nairobi, Kenya and Université Paris-Sud 11, 91405 Orsay, France 3ICIPE, Stemborer Biocontrol Program, PO Box 30772-00100, Nairobi, Kenya Key words. Hymenoptera, Braconidae, Cotesia sesamiae, C. flavipes, Lepidoptera, Pyralidae, Eldana saccharina, Noctuidae, Busseola fusca, Chilo partellus, parasitoids, host recognition, host acceptance, stemborers, Africa Abstract. The host recognition and acceptance behaviour of two braconid larval parasitoids (Cotesia sesamiae and C. flavipes) were studied using natural stemborer hosts (i.e., the noctuid Busseola fusca for C. sesamiae, and the crambid Chilo partellus for C. flavi- pes) and a non-host (the pyralid Eldana saccharina). A single larva was introduced into an arena together with a female parasitoid and the behaviour of the wasp recorded until it either stung the larva or for a maximum of 5 min if it did not sting the larva. There was a clear hierarchy of behavioural steps, which was similar for both parasitoid species. In the presence of suitable host larvae, after a latency period of 16–17 s, the wasp walked rapidly drumming the surface with its antennae until it located the larva. -
NEWSLETTER• of the MICHIGAN ENTOMOLOGICAL SOCIETY
NEWSLETTER• of the MICHIGAN ENTOMOLOGICAL SOCIETY Volume 38, Numbers 4 December, 1993 Impacts ofBt on Non-Target Lepidoptera John W. Peacock, David L. Wagner, and Dale F. Schweitzer USDA Forest Service, Hamden, CT; University of Connecticut, Storrs, CT; and The Nature Conservancy, Port Norris, NT, respectively Introduction gypsy moth in Oregon. Sample et a1. ing attempts bycertain birds. In another (1 993) have likewise reported a signifi study, Bellocq et al. (1992) showed that Bacillus thuringiensis Berliner var. cant reduction inspecies abundance and the use of Btk increased immigration kurstaki (Btk) is one of the pesticides richness in non-target Lepidoptera in rates andcaused d ietary shifts inshrews. most commonly employed against lepi field studies in eastern West Virginia. We report here a summary of our dopteran forest pests. In the eastern U.S., James et al. (1993) haveshown thatBtk is studies aimed at determining the effect where millionsofhectares of deciduous toxic to late, but not early, instar larvae of Btko n non-target Lepidoptera inboth forest have been defoliated by the ''Eu of the beneficial cinnabar moth, Tyria laboratoryand field studies. Laboratory ropean" gypsy moth, Lymantria dispar jacobaeae (L.). bioassays were conducted on larvae in (L.), Btk has been used extenSively to In addition to its direct effects on seven families of native eastern U.S. slow the spread of this pest and to re native Lepidoptera, Btk can indirectly Macrolepidoptera. Field studies were duce defoliation. In 1992 alone, over affect other animals that rely on lepi carried out in Rockbridge County, Vir 300,000 ha were treated with Btk, in dopterous larvae as a primary source of ginia, and were the first to evaluate non cluding gypsy moth suppression activi food. -
Report-VIC-Croajingolong National Park-Appendix A
Croajingolong National Park, Victoria, 2016 Appendix A: Fauna species lists Family Species Common name Mammals Acrobatidae Acrobates pygmaeus Feathertail Glider Balaenopteriae Megaptera novaeangliae # ~ Humpback Whale Burramyidae Cercartetus nanus ~ Eastern Pygmy Possum Canidae Vulpes vulpes ^ Fox Cervidae Cervus unicolor ^ Sambar Deer Dasyuridae Antechinus agilis Agile Antechinus Dasyuridae Antechinus mimetes Dusky Antechinus Dasyuridae Sminthopsis leucopus White-footed Dunnart Felidae Felis catus ^ Cat Leporidae Oryctolagus cuniculus ^ Rabbit Macropodidae Macropus giganteus Eastern Grey Kangaroo Macropodidae Macropus rufogriseus Red Necked Wallaby Macropodidae Wallabia bicolor Swamp Wallaby Miniopteridae Miniopterus schreibersii oceanensis ~ Eastern Bent-wing Bat Muridae Hydromys chrysogaster Water Rat Muridae Mus musculus ^ House Mouse Muridae Rattus fuscipes Bush Rat Muridae Rattus lutreolus Swamp Rat Otariidae Arctocephalus pusillus doriferus ~ Australian Fur-seal Otariidae Arctocephalus forsteri ~ New Zealand Fur Seal Peramelidae Isoodon obesulus Southern Brown Bandicoot Peramelidae Perameles nasuta Long-nosed Bandicoot Petauridae Petaurus australis Yellow Bellied Glider Petauridae Petaurus breviceps Sugar Glider Phalangeridae Trichosurus cunninghami Mountain Brushtail Possum Phalangeridae Trichosurus vulpecula Common Brushtail Possum Phascolarctidae Phascolarctos cinereus Koala Potoroidae Potorous sp. # ~ Long-nosed or Long-footed Potoroo Pseudocheiridae Petauroides volans Greater Glider Pseudocheiridae Pseudocheirus peregrinus -
Report Template
Gumleaf Skeletonizer (GLS) monitoring using pheromone baited moth traps 2011-2014 Janet D. Farr and Allan J. Wills Occasional Report June 2014 Occasional Report Department of Parks and Wildlife Locked Bag 104 Bentley Delivery Centre WA 6983 Phone: (08) 9219 9000 Fax: (08) 9334 0498 www.dpaw.wa.gov.au © Department of Parks and Wildlife on behalf of the State of Western Australia 2014 June 2014 This work is copyright. You may download, display, print and reproduce this material in unaltered form (retaining this notice) for your personal, non-commercial use or use within your organisation. Apart from any use as permitted under the Copyright Act 1968, all other rights are reserved. Requests and enquiries concerning reproduction and rights should be addressed to the Department of Parks and Wildlife. This report was prepared by Allan Wills Questions regarding the use of this material should be directed to: Allan Wills Science and Conservation Division Department of Parks and Wildlife Locked Bag 104 Bentley Delivery Centre WA 6983 Phone: 0438996352 Email: [email protected] The recommended reference for this publication is: Janet D. Farr and Allan J. Wills, 2014, Gumleaf Skeletonizer (GLS) monitoring using pheromone baited moth traps 2011-2014, Department of Parks and Wildlife, Perth. Disclaimer Data presented in this report should not be inferred to be indicative of future Gumleaf Skeletonizer population changes or future damage caused by Gumleaf Skeletonizer. This document is available in alternative formats on request. Please note: urls in this document which conclude a sentence are followed by a full point. If copying the url please do not include the full point. -
Gumleaf Skeletoniser Biocontrol: a Lesson in Patience
THE JOINT FORCES OF CSIRO & SCION Lisa Berndt, Michelle Watson and Tara Murray Ensis Forest Biosecurity and Protection BiologicalBiological controlcontrol ofof gumleafgumleaf skeletoniser,skeletoniser, paropsisparopsis andand buddleiabuddleia March 2007 THE JOINT FORCES OF CSIRO & SCION Gumleaf skeletoniser Uraba lugens (Nolidae) • Australian eucalypt defoliator • In Auckland since 2001 • Spreading to Waikato, Northland, BOP • Threat to plantations, amenity trees, public health • Attacking new host plant species THE JOINT FORCES OF CSIRO & SCION GLS biocontrol • 4 potential parasitoids identified • ERMA permission to import 2004 • Develop rearing & host testing methods 2004-2007 (2 species) Eriborus sp. Photos: Geoff Allen & John Barran Euplectrus sp. Cotesia urabae Dolichogenidea eucalypti THE JOINT FORCES OF CSIRO & SCION Success: rearing • Rearing method finally successful • Solving mating problems key THE JOINT FORCES OF CSIRO & SCION Success: host testing • Methods developed • Nearly complete for two species • Nine more species to test • Strong preference for uraba THE JOINT FORCES OF CSIRO & SCION Paropsis biocontrol • Major eucalypt pest • Previously controlled by parasitoid Enoggera nissaui • Biocontrol disrupted by hyperparasitoid in North Island since 2002 Enoggera nassaui on P. charybdis egg • Second parasitoid (Neopolycystus insectifurax) not as effective • Most plantations sprayed annually now THE JOINT FORCES OF CSIRO & SCION Paropsis charybdis Current research • PhD student Tara Murray (2nd year) • Studying biology of hyperparasitoid -
Check List of Noctuid Moths (Lepidoptera: Noctuidae And
Бiологiчний вiсник МДПУ імені Богдана Хмельницького 6 (2), стор. 87–97, 2016 Biological Bulletin of Bogdan Chmelnitskiy Melitopol State Pedagogical University, 6 (2), pp. 87–97, 2016 ARTICLE UDC 595.786 CHECK LIST OF NOCTUID MOTHS (LEPIDOPTERA: NOCTUIDAE AND EREBIDAE EXCLUDING LYMANTRIINAE AND ARCTIINAE) FROM THE SAUR MOUNTAINS (EAST KAZAKHSTAN AND NORTH-EAST CHINA) A.V. Volynkin1, 2, S.V. Titov3, M. Černila4 1 Altai State University, South Siberian Botanical Garden, Lenina pr. 61, Barnaul, 656049, Russia. E-mail: [email protected] 2 Tomsk State University, Laboratory of Biodiversity and Ecology, Lenina pr. 36, 634050, Tomsk, Russia 3 The Research Centre for Environmental ‘Monitoring’, S. Toraighyrov Pavlodar State University, Lomova str. 64, KZ-140008, Pavlodar, Kazakhstan. E-mail: [email protected] 4 The Slovenian Museum of Natural History, Prešernova 20, SI-1001, Ljubljana, Slovenia. E-mail: [email protected] The paper contains data on the fauna of the Lepidoptera families Erebidae (excluding subfamilies Lymantriinae and Arctiinae) and Noctuidae of the Saur Mountains (East Kazakhstan). The check list includes 216 species. The map of collecting localities is presented. Key words: Lepidoptera, Noctuidae, Erebidae, Asia, Kazakhstan, Saur, fauna. INTRODUCTION The fauna of noctuoid moths (the families Erebidae and Noctuidae) of Kazakhstan is still poorly studied. Only the fauna of West Kazakhstan has been studied satisfactorily (Gorbunov 2011). On the faunas of other parts of the country, only fragmentary data are published (Lederer, 1853; 1855; Aibasov & Zhdanko 1982; Hacker & Peks 1990; Lehmann et al. 1998; Benedek & Bálint 2009; 2013; Korb 2013). In contrast to the West Kazakhstan, the fauna of noctuid moths of East Kazakhstan was studied inadequately.