Area-Wide Survey of Tree Fruit Pests Including Nurseries in Utah – 2004
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1. Cherry Bark Tortrix (CBT), Cherry Washington. Thetrees Have
III. Stone Fruits a. Biology 1. Cherry Bark Tortrix (CBT), cherry Michael W. Klaus Washington State Department ofAgriculture 2015 S. First Street Yakima, WA 98903 Thefirst U.S. detection of CBT was reported by WSDA on March 29,1991. The find wasa larval collection from an ornamental cherry treeat the PeaceArch StatePark, Blaine, Whatcom County, Washington. Thetrees have extensive tunneling throughout the bark of thetrunk andthe bark ofthe larger limbs. The tunneling has nearly girdled thetrees. Park gardeners consider these sixty yearold Mt. Fuji cherry trees to bea total loss andwill be removing them soon. The cherry bark tortrix (CBT), Enarmonia formosana (Scopoli), isnative to Europe and Siberia. Itwas first mentioned as a pestofstonefruits in Europe by Kollar in 1837 andas a pest in the British Isles byTheobald (1909). CBT has been reported tocause serious damage in stone fruit, apple, pearand other trees(Thomsen 1920, Samal 1926). CBT issometimes locally serious, but is generally considered tobe a pest of minor importance in the British Isles (Massee,1954). Biology and Identification CBT feeds on the bark and sapwood ofa variety ofplants ofthe family Rosaceaeincluding Prunus (cherry, plum, peach, apricot, nectarine and almond), Malus (apple), Pvrus (pear), Pyracantha (firethom), Sorbus(mountain ash) and Cvdonia (quince). Infested hosts identified in Washington to date (via larval collections, voucher specimens in WSDA Yakima collection) havebeen mature cherryand apple trees. A CBT infestation of mountain ash inVancouver, B.C. Canadawas reported in June of 1992. CBT is a moth in the family Tortricidae. It is related to another important tortricid applepest, the codling moth. Codling moth was once named Enarmonia pomonella. -
Data Sheets on Quarantine Pests
EPPO quarantine pest Prepared by CABI and EPPO for the EU under Contract 90/399003 Data Sheets on Quarantine Pests Cydia prunivora IDENTITY Name: Cydia prunivora (Walsh) Synonyms: Grapholitha prunivora (Walsh) Enarmonia prunivora Walsh Semasia prunivora Walsh Laspeyresia prunivora Walsh Taxonomic position: Insecta: Lepidoptera: Tortricidae Common names: Lesser appleworm, plum moth (English) Petite pyrale (French) Bayer computer code: LASPPR EPPO A1 list: No. 36 EU Annex designation: II/A1 - as Enarmonia prunivora HOSTS The main natural host is Crataegus spp., especially the larger-fruited species such as C. holmesiana. C. prunivora readily attacks apples, plums and cherries. It has been recorded on peaches, roses and Photinia spp. Larvae may also develop in galls of Quercus and Ulmus. For more information, see Chapman & Lienk (1971). GEOGRAPHICAL DISTRIBUTION C. prunivora is indigenous on wild Crataegus spp. in eastern North America (north-eastern states of USA and adjoining provinces of Canada) and has spread onto fruit trees in other parts of North America (western Canada and USA). EPPO region: Absent. Asia: China (Heilongjiang only, unconfirmed). The record given for India in the previous edition is erroneous. North America: Canada (British Columbia, eastern provinces), USA (practically throughout). EU: Absent. Distribution map: See CIE (1975, No. 341). BIOLOGY The life and seasonal history is similar to that of the European codling moth, Cydia pomonella. C. prunivora overwinters as a full-grown larva in a cocoon in debris on the ground or in crevices in the trunks of host trees. In the western fruit district of New York State, USA, and in Ontario, Canada, pupation takes place in May and lasts 2-3 weeks. -
Yponomeuta Malinellus
Yponomeuta malinellus Scientific Name Yponomeuta malinellus (Zeller) Synonyms: Hyponomeuta malinella Zeller Hyponomeuta malinellus Zeller Yponomeuta malinella Yponomeuta padella (L.) Yponomeuta padellus malinellus Common Names Apple ermine moth, small ermine moth Figure 1. Y. malinellus adult (Image courtesy of Eric LaGasa, Washington State Department of Agriculture, Bugwood.org). Type of Pest Caterpillar Taxonomic Position Class: Insecta, Order: Lepidoptera, Family: Yponomeutidae Reason for Inclusion 2012 CAPS Additional Pests of Concern Pest Description Eggs: “The individual egg has the appearance of a flattened, yellow, soft disc with the centre area slightly raised, and marked with longitudinal ribbings. Ten to eighty eggs are deposited in overlapping rows to form a flattened, slightly convex, oval egg mass. At the time of deposition, the egg mass is covered with a glutinous substance, which on exposure to air forms a resistant, protective coating. This coating not only acts as an egg-shield but provides an ideal overwintering site for the diapausing first-instar larvae. The egg mass is yellow at first but then darkens until eventually it is grey-brown and resembles the bark of apple twigs. Egg masses average 3-10 mm [0.12-0.39 in] in length and 4 mm [0.16 in] in width but vary considerably in size and shape” (CFIA, 2006). Larvae: “Grey, yellowish-grey, greenish-brown, and greyish-green larvae have been reported. The mature larva is approximately 15-20 mm [0.59-0.79 in] in length; the anterior and posterior extremities are much narrower than the remainder of the body. There are 2 conspicuous laterodorsal black dots on each segment from the mesothorax to the 8th abdominal segment. -
International Symposium on Biological Control of Arthropods 424 Poster Presentations ______
POSTER PRESENTATIONS ______________________________________________________________ Poster Presentations 423 IMPROVEMENT OF RELEASE METHOD FOR APHIDOLETES APHIDIMYZA (DIPTERA: CECIDOMYIIDAE) BASED ON ECOLOGICAL AND BEHAVIORAL STUDIES Junichiro Abe and Junichi Yukawa Entomological Laboratory, Kyushu University, Japan ABSTRACT. In many countries, Aphidoletes aphidimyza (Rondani) has been used effectively as a biological control agent against aphids, particularly in greenhouses. In Japan, A. aphidimyza was reg- istered as a biological control agent in April 1999, and mass-produced cocoons have been imported from The Netherlands and United Kingdom since mass-rearing methods have not yet been estab- lished. In recent years, the effect of imported A. aphidimyza on aphid populations was evaluated in greenhouses at some Agricultural Experiment Stations in Japan. However, no striking effect has been reported yet from Japan. The failure of its use in Japan seems to be caused chiefly by the lack of detailed ecological or behavioral information of A. aphidimyza. Therefore, we investigated its ecological and behavioral attributes as follows: (1) the survival of pupae in relation to the depth of pupation sites; (2) the time of adult emergence in response to photoperiod during the pupal stage; (3) the importance of a hanging substrate for successful mating; and (4) the influence of adult size and nutrient status on adult longev- ity and fecundity. (1) A commercial natural enemy importer in Japan suggests that users divide cocoons into groups and put each group into a plastic container filled with vermiculite to a depth of 100 mm. However, we believe this is too deep for A. aphidimyza pupae, since under natural conditions mature larvae spin their cocoons in the top few millimeters to a maxmum depth of 30 mm. -
Area-Acct & Title-Project Investigator4
Washington State University Sponsored Programs Services Area/Budget/Account - FY 03 - Direct and Facilities & Administrative Costs - 06/30/2003 AR BUD CFDA SPG ACCOUNT EA GET NO M ACCOUNT DIRECT COSTS F&A COSTS TOTAL PRIMARY PI OTHER PI TITLE 1 2926 12-999 12F 2926-0001 25,037.85 0 25,037.85 HERBST C JOHANSEN W / B GRANT BASIC AND ADVANCE 1 2933 84-342 12G 2933-0004 5,152.80 412.22 5,565.02 HALL L BROWN G / BROWPREPARE TOMORROW'S TEACHERS/USE TECH 1 2934 - 14N 2934-0010 28,589.78 0 28,589.78 KILGORE S STONE C VISIBLE KNOWLEDGE PROJECT 1 2934 84-336 12G 2934-0011 13,374.87 1,069.98 14,444.85 LAW R MOORE M CO-TEACH 1 2934 45-999 12W 2934-0012 -454.49 0 -454.49 KILGORE S CONDON W NMC VISUAL EVIDENCE & US PAST 1 2936 84-116 12G 2936-0007 134,239.30 8,594.81 142,834.11 CONDON W KELLY-RILEY D / FOSTER CRITICAL THINKING/FACULTY PRACTICE 2 1170 84-042 12G 1170-0011 32,525.00 2,602.01 35,127.01 JAMISON A STUDENT SUPPORT SERVICES PROGRAM 2 1170 84-042 12G 1170-0012 125.62 0 125.62 JAMISON A STUDENT SUPPORT SERVICES PROGRAM 2 1170 84-042 12G 1170-0013 158,877.13 7,404.48 166,281.61 JAMISON A STUDENT SUPPORT SERVICES PROG 2 1170 84-042 12G 1170-0014 2,488.62 0 2,488.62 JAMISON A STUDENT SUPPORT SERVICES PROG SUPPL 2 1170 84-042 12G 1170-0015 9,800.00 0 9,800.00 JAMISON A STUDENT SUPPORT SERVICES PROG GRANT AID 2 2968 - 14A 2968-0036 0 270.95 270.95 VOSS E SPECIAL NEEDS CAPACITY PROJECT 2 2968 - 14A 2968-0037 0 117.14 117.14 VOSS E INFANT CARE PROJECT 2 2968 93-596 14A 2968-0038 721.14 80.12 801.26 CILLAY V VOSS E CHILD CARE RES & REF/BLDG BLOCKS -
Organisme De Quarantaine OEPP Préparé Par Le CABI Et L'oepp Pour L'ue Sous Contrat 90/399003
Organisme de quarantaine OEPP Préparé par le CABI et l'OEPP pour l'UE sous Contrat 90/399003 Fiche informative sur les organismes de quarantaine Cydia packardi IDENTITE Nom: Cydia packardi (Zeller) Synonymes: Grapholita packardi Zeller Steganoptycha pyricolana Murtfeldt Enarmonia packardi (Zeller) Enarmonia pyricolana (Murtfeldt) Laspeyresia packardi (Zeller) Laspeyresia pyricolana (Murtfeldt) Classement taxonomique: Insecta: Lepidoptera: Tortricidae Noms communs: cherry fruitworm (anglais) phalène des cerises (français/canadien) Notes sur la taxonomie et la nomenclature: en raison de différences signalées dans la saisonnalité et dans le cycle de vie sur différentes plantes-hôtes, Chapman & Lienk (1971) ont émis l'idée que C. packardi pourrait comprendre soit plusieurs espèces soit des souches adaptées à des régimes alimentaires. D'ailleurs, Miller (1987) cite Chapman & Lienk (1971) pour justifier sa définition de C. packardi en tant que “complexe d'espèces” bien que ces auteurs aient finalement conclu que C. packardi devait être considéré comme une espèce unique tant que des recherches plus approfondies n'auraient pas été menées. Il faut d'ailleurs remarquer que les caractéristiques biologiques de cette espèce sur pommier ont été définies sur la base d'anciennes études qui ne spécifiaient pas la méthode d'élevage (c'est à dire ne spécifiant pas s'il s'agissait d'études en laboratoire ou en plein champ), et que, de plus, ces caractéristiques n'ont pas été confirmées par des études plus précises. Cependant, l'uniformité des caractères morphologiques des spécimens de C. packardi tend à prouver qu'il s'agirait plutôt d'une espèce unique. Code informatique Bayer: LASPPA Liste A1 OEPP: n° 209 Désignation Annexe UE: II/A1, sous l'appellation Enarmonia packardi PLANTES-HOTES Les principales plantes-hôtes cultivées sont le cerisier, le pommier et Vaccinium spp. -
Pests in Northwestern Washington Prompted a 1994-1995 CAPS Survey of Apple Trees to Identify All Leaf-Feeding Apple Pests Currently in Whatcom County
6. Biology / Phenology a. Biology 1. Exotic Fruit Tree Pests in Whatcom County, Washington Eric LaGasa Plant Services Div., Wash. St. Dept. of Agriculture P.O. Box 42560, Olympia, Washington 98504-2560 (360) 902-2063 [email protected] The Washington State Department of Agriculture (WSDA) has conducted detection surveys and other field projects for exotic pests since the mid-1980's, with funding provided by the USDA/ APHIS Cooperative Agricultural Pest Survey (CAPS) program. Recent discovery of several exotic fruit tree pests in northwestern Washington prompted a 1994-1995 CAPS survey of apple trees to identify all leaf-feeding apple pests currently in Whatcom County. Additional exotic apple pest species, new to either the region or U.S. were discovered. This paper presents some brief descriptions of species detected in that project, and other exotic fruit tree pest species discovered in northwest Washington since 1985. Table 1. - Exotic Fruit Tree Pests New to Northwestern Washington State - 1985 to 1995 green pug moth - Geometridae: Chloroclystis rectangulata (L.) An early, persistent European pest of apple, pear, cherry and other fruit trees. Larvae attack buds, blossoms, and leaves from March to June. Damage to blossoms causes considerable deformation of fruit. Larvae are common in apple blossoms in Whatcom County, where it was first reared from apple trees in 1994. This pest, new to North America, was also recently detected in the northeastern U.S. Croesia holmiana - Tortricidae: Croesia holmiana (L.) A common pest of many fruit trees and ornamental plants in Europe and Asia, where it is considered a minor problem. Spring larval feeding affects only leaves. -
International Symposium on Biological Control of Arthropods 2005
Agusti et al. _________________________________________________________________________ Session 12: Environmental Risk Assessment of Invertebrate Biological Control Agents ESTIMATING PARASITISM LEVELS IN OSTRINIA NUBILALIS HÜBNER (LEPIDOPTERA: CRAMBIDAE) FIELD POPULATIONS USING MOLECULAR TECHNIQUES Nuria AGUSTI1, Denis BOURGUET2, Thierry SPATARO3, and Roger ARDITI3 1Dept. de Proteccio Vegetal Institut de Recerca i Tecnologia Agroalimentaries (IRTA) 08348 Cabrils (Barcelona), Spain [email protected] 2Centre de Biologie et de Gestion des Populations (CBGP) Institut National de la Recherche Agronomique (INRA) Campus International de Baillarguet CS 30 016, 34988 Montferrier / Lez cedex, France [email protected] 3Ecologie des populations et communautés 76 Institut National Agronomique Paris-Grignon (INA P-G) 75231 Paris cedex 05, France [email protected] [email protected] Accurate detection and identification of parasitoids are critical to the success of IPM pro- grams to detect unusual variations of the density of these natural enemies, which may follow changes in agricultural practices. For such purposes specific molecular markers to detect Lydella thompsoni (Herting) and Pseudoperichaeta nigrolineata (Walker) (Diptera: Tachinidae) within the european corn borer, Ostrinia nubilalis (Hübner) (Lepidoptera: Crambidae) have been developed. Primers amplifying fragments of the mitochondrial cytochrome oxidase I (COI) gene were designed following alignment of comparable sequences for a range of parasitoid and host species. Each of the primer pairs proved to be species-specific to one of those ta- chinid species, amplifying DNA fragments of 191 and 91 bp in length for L. thompsoni and P. nigrolineata, respectively. This DNA-based technique allowed to perform a molecular detec- tion of parasitism in natural populations of O. nubilalis. Molecular evaluation of parasitism was compared with the traditional method of rearing ECB populations in controlled conditions before breaking off the diapause. -
Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation
CHAPTER THIRTEEN Small Ermine Moths Role of Pheromones in Reproductive Isolation and Speciation MARJORIE A. LIÉNARD and CHRISTER LÖFSTEDT INTRODUCTION Role of antagonists as enhancers of reproductive isolation and interspecific interactions THE EVOLUTION TOWARDS SPECIALIZED HOST-PLANT ASSOCIATIONS SUMMARY: AN EMERGING MODEL SYSTEM IN RESEARCH ON THE ROLE OF SEX PHEROMONES IN SPECIATION—TOWARD A NEW SEX PHEROMONES AND OTHER ECOLOGICAL FACTORS “SMALL ERMINE MOTH PROJECT”? INVOLVED IN REPRODUCTIVE ISOLATION Overcoming the system limitations Overview of sex-pheromone composition Possible areas of future study Temporal and behavioral niches contributing to species separation ACKNOWLEDGMENTS PHEROMONE BIOSYNTHESIS AND MODULATION REFERENCES CITED OF BLEND RATIOS MALE PHYSIOLOGICAL AND BEHAVIORAL RESPONSE Detection of pheromone and plant compounds Introduction onomic investigations were based on examination of adult morphological characters (e.g., wing-spot size and color, geni- Small ermine moths belong to the genus Yponomeuta (Ypo- talia) (Martouret 1966), which did not allow conclusive dis- nomeutidae) that comprises about 75 species distributed glob- crimination of all species, leading to recognition of the so- ally but mainly in the Palearctic region (Gershenson and called padellus-species complex (Friese 1960) which later Ulenberg 1998). These moths are a useful model to decipher proved to include five species (Wiegand 1962; Herrebout et al. the process of speciation, in particular the importance of eco- 1975; Povel 1984). logical adaptation driven by host-plant shifts and the utiliza- In the 1970s, “the small ermine moth project” was initiated tion of species-specific pheromone mating-signals as prezy- to include research on many aspects of the small ermine gotic reproductive isolating mechanisms. -
Capital-Breeding Lepidoptera
VOLUME 59, NUMBER 3 143 Journal of the Lepidopterists’ Society 59(3), 2005, 143–160 EXTRINSIC EFFECTS ON FECUNDITY-MATERNAL WEIGHT RELATIONS IN CAPITAL-BREEDING LEPIDOPTERA WILLIAM E. MILLER Department of Entomology, University of Minnesota, St. Paul, Minnesota 55108 USA email: [email protected] ABSTRACT. Capital-breeding Lepidoptera depend for reproduction on metabolic resources assembled either entirely or primarily by their larvae, the former termed 'perfect' the latter 'imperfect'. Empirical evidence suggests that maternal size determines capi- tal-breeder fecundity. The fecundity-maternal size relation is usually formulated as F = bW + a, where F is fecundity, W is final ma- ternal size in units such as weight of newly transformed pupae, b is the slope, and a the intercept. Exhaustive search yielded 71 fe- cundity-maternal pupal weight relations for 41 capital breeders in 15 families, 58 of which, including 2 previously unpublished, were based on individual specimens, and 13 on grouped specimens. In 22 individual-specimen relations, cohorts divided into 2 or more subgroups were reared simultaneously at different temperatures, on different diets, or exposed to other extrinsic factors. These 22 'multiform' relations were compared with 36 'uniform' relations, and where possible cohort subgroups were compared. Pupal weights of cohort subgroups were affected much oftener than underlying slopes and intercepts. Individual-specimen slopes based on transformed data ranged 0.52-2.09 with a mean and standard error of 1.13±0.04, and slopes did not differ significantly among perfect, imperfect, multiform, and uniform categories. Despite the evident similarity, one relation does not apply to all capital breed- ers. -
Biological-Control-Programmes-In
Biological Control Programmes in Canada 2001–2012 This page intentionally left blank Biological Control Programmes in Canada 2001–2012 Edited by P.G. Mason1 and D.R. Gillespie2 1Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada; 2Agriculture and Agri-Food Canada, Agassiz, British Columbia, Canada iii CABI is a trading name of CAB International CABI Head Offi ce CABI Nosworthy Way 38 Chauncey Street Wallingford Suite 1002 Oxfordshire OX10 8DE Boston, MA 02111 UK USA Tel: +44 (0)1491 832111 T: +1 800 552 3083 (toll free) Fax: +44 (0)1491 833508 T: +1 (0)617 395 4051 E-mail: [email protected] E-mail: [email protected] Website: www.cabi.org Chapters 1–4, 6–11, 15–17, 19, 21, 23, 25–28, 30–32, 34–36, 39–42, 44, 46–48, 52–56, 60–61, 64–71 © Crown Copyright 2013. Reproduced with the permission of the Controller of Her Majesty’s Stationery. Remaining chapters © CAB International 2013. All rights reserved. No part of this publication may be reproduced in any form or by any means, electroni- cally, mechanically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Biological control programmes in Canada, 2001-2012 / [edited by] P.G. Mason and D.R. Gillespie. p. cm. Includes bibliographical references and index. ISBN 978-1-78064-257-4 (alk. paper) 1. Insect pests--Biological control--Canada. 2. Weeds--Biological con- trol--Canada. 3. Phytopathogenic microorganisms--Biological control- -Canada. -
Table of Contents
Table of Contents Table of Contents ............................................................................................................ 1 Authors, Reviewers, Draft Log ........................................................................................ 3 Introduction to Reference ................................................................................................ 5 Introduction to Stone Fruit ............................................................................................. 10 Arthropods ................................................................................................................... 16 Primary Pests of Stone Fruit (Full Pest Datasheet) ....................................................... 16 Adoxophyes orana ................................................................................................. 16 Bactrocera zonata .................................................................................................. 27 Enarmonia formosana ............................................................................................ 39 Epiphyas postvittana .............................................................................................. 47 Grapholita funebrana ............................................................................................. 62 Leucoptera malifoliella ........................................................................................... 72 Lobesia botrana ....................................................................................................