Allium Leaf Miner Is Spreading Around the UK at a Steady Rate with Clusters of Infestation Around the Midlands and London
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Sustainable Crop Protection
SUSTAINABLE CROP PROTECTION Results from the Pesticide Risk Reduction Program An Integrated Approach to Management of Leek Moth 10 years of collaborative research, development and knowledge transfer Photo credits: A. Brauner Figure 1: Leek Moth (Acrolepiopsis assectella) at key developmental stages Background Establishing Base Knowledge – The leek moth, Acrolepiopsis assectella, (Figure 1) is an invasive Leek moth life history in Canada alien species from Europe that causes damage to onions, leeks As a new pest to Canada, initial work focused on determining and garlic. Larvae cause damage when they penetrate the young the life cycle of the pest under Eastern Ontario conditions. leaves and flowers of the crop in order to feed (Figure 2). This Pheromone traps were used to monitor flight patterns and feeding weakens and withers the plant reducing the value of the numbers of adult leek moth during the growing season, while crop, and in some cases renders it unmarketable. First detected field populations of leek moth larvae and pupae were estimated in Eastern Ontario in 1993 and Quebec in 2001, leek moth has through destructive plant sampling. Assessment of garlic scapes rapidly expanded its range and, as of 2013, was detected as far as and bulbs were used to estimate damage to marketable products. Southwestern Ontario, Prince Edward Island and New York State. It was found that the development of leek moth populations in The Pesticide Risk Reduction Program of Agriculture and Canada requires 441.7 day-degrees from egg to adult. In the Agri-Food Canada’s (AAFC) Pest Management Centre has, over Ottawa area, pheromone trap data indicated that there are three the past ten years, supported several projects towards the flight periods: a spring flight of adults that overwintered, an early development of an Integrated Pest Management (IPM) strategy summer flight of 1st generation adults and a late summer flight of to address this emerging pest issue. -
(Aphis Gossypii (Glov.) and Bemisia Tabaci (G.) in the New Varieties Second Plant (After Canola) in the Golestan Province of Iran
Study on Population Changes of Important Sucking – Pests (Aphis Gossypii (Glov.) and Bemisia Tabaci (G.) in the New Varieties Second Plant (After Canola) in the Golestan Province of Iran. Taghi Darvish, Mojeni ( [email protected] ) Cotton Research Institute Mohammadreza Zangi Cotton Research Institute Research Keywords: Cotton variety, Sucking - pests, Golestan province Posted Date: June 21st, 2021 DOI: https://doi.org/10.21203/rs.3.rs-585098/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/12 Abstract Investigating the population dynamic of important cotton pests on new cotton varieties is important. Cotton cultivars have important pests such as thrips, aphids, whitey and bollworm. Considering the premature cultivars with proper yield for second cultivation in cotton-growing Golestan province at the north of Iran, this study seems necessary. This genotypes was cultivated with 9 treatments in 4 replicates. A completely randomized block design was carried out in Hashem Abad research station in a spray-free plot with the dimensions of 30 × 80 cm in 2018-2019 years. According to the results of this study, analysis of variance of two years showed that the yield of N2G80 with 1538 g in the plot with 41.7% lint percentage had the highest yield, and M13 with 685 g in the plot and 35.8% lint percentage in the lowest yield they had.The infestation rate of the genotypes tested in the population of green aphid of cotton in K880-2 and Golestan® cultivars was 48.88 and 40.31 in aphid with the highest density, and the SKT-133 and TBL-60 genotype respectively with 27.15 and 29.11 aphids per leaf had the least infestation. -
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Egypt. J. Agric. Res., 97 (1), 2019 159 SUSCEPTIBILITY OF SOME SOYBEAN VARIETIES TO CERTAIN PIERCING-SUCKING INSECTS UNDER THE FIELD CONDITIONS OF NORTH DELTA MESBAH, I.I.1; E.M.E. KHALAFALLA2; GHADA M. EISSA2; FATMA H. HEGAZY1 AND M.A. KHATTAB2 1. Plant Protection Dept. Fac. of Agric., Tanta Univ., Egypt 2. Plant Protection Research Institute, ARC. Dokki, Egypt (Manuscript received 6 January 2019) Abstract olerant varieties to insect species represent one of the simplest and important methods of insect pest control to minimize the insecticide T hazards. Therefore, susceptibility of five soybean varieties to infestation with some piercing-sucking insects: aphids, Aphis spp.; whitefly, Bemisia tabaci (Genn.) and leafhoppers, Empoasca spp. were evaluated at Sakha Agric. Res. Station Farm, Kafr El-Sheikh Governorate during 2016 and 2017 seasons. The obtained results showed significant differences in susceptibility between the tested soybean varieties to the mentioned insects for every season and from season to another. In general, the population density of whitefly and aphids were higher in the first season than the second one, while the reverse was found for leafhoppers. Based on the grand mean number of the two study seasons, variety Crawford was significantly the most infested variety to infestation with leafhoppers and aphids, while the least infested variety for aphids was Giza35 and for leafhoppers was Hybrid30. As for the whitefly, Giza35 significantly was the most infested variety, while Crawford was the least infested one. In respect to the resistance status of the tested varieties to the insects, Crawford and Hybrid30 showed susceptiblity to aphid infestation, while the other varieties exhibited low resistance. -
Acrolepiopsis Assectella
Acrolepiopsis assectella Scientific Name Acrolepiopsis assectella (Zeller, 1893) Synonym: Lita vigeliella Duponchel, 1842 Common Name Leek moth, onion leafminer Type of Pest Moth Taxonomic Position Class: Insecta, Order: Lepidoptera, Family: Acrolepiidae Figures 1 & 2. Adult male (top) and female (bottom) Reason for Inclusion of A. assectella. Scale bar is 1 mm (© Jean-François CAPS Community Suggestion Landry, Agriculture & Agri-Food Canada, 2007). Pest Description Eggs: “Roughly oval in shape with raised reticulated sculpturing; iridescent white” (Carter, 1984). Eggs are 0.5 by 1 0.2 mm (< /16 in) (USDA, 1960). Larvae: “Head yellowish brown, sometimes with reddish brown maculation; body yellowish green; spiracles surrounded by sclerotised rings, on abdominal segments coalescent with SD pinacula, these grayish brown; prothoracic and anal plates yellow with brown maculation; thoracic legs yellowish brown’ crochets of abdominal prologs arranged in uniserial circles, each enclosing a short, longitudinal row of 3–5 crochets” 1 (Carter, 1984). Larvae are about 13 to 14 mm (approx. /2 in) long (McKinlay, 1992). Pupae: “Reddish brown; abdominal spiracles on raised tubercles; cremaster abruptly terminated, dorsal lobe with a Figure 3. A. assectella larvae rugose plate bearing eight hooked setae, two rounded ventral on stem of elephant garlic lobes each bearing four hooked setae” (Carter, 1984). The (eastern Ontario, June 2000) (© 1 cocoon is 7 mm (approx. /4 in) long (USDA, 1960). “The Jean-François Landry, cocoon is white in colour and is composed of a loose net-like Agriculture & Agri-Food Canada, 2007). structure” (CFIA, 2012). Last updated: August 23, 2016 9 Adults: “15 mm [approx. /16 in wingspan]. Forewing pale brown, variably suffused with blackish brown; terminal quarter sprinkled with white scales; a distinct triangular white spot on the dorsum near the middle. -
Diamondback Moth: Plutella Xylostella (Linnaeus)
Diamondback Moth: Plutella xylostella Monitoring Protocol Host plants: Plants belong to the family Brassicaceae such as canola, mustard, broccoli, cauliflower, cabbage. Identification, Life cycle and Damage: Adults: Adult moths are approximately 12 mm long, with a 18-20 mm wing span (Figure 1). They are grey or brownish with white marks on the inner margin of the forewing. Their name is derived from a series of diamond shaped figures formed by these white marks when the wings are folded at rest. Eggs: Eggs are oval, yellowish-white and tiny. They are laid on the leaf surface the leaf surface singly or in small groups (Figure 2). Figure 1: Adult- 16 days Figure 2: Eggs- 5-6 days Figure 3: Larva- 10-30 days Figure 4: Pupa- 7-14 days Larvae: Diamondback moth has four larval stages. The first stage is a leaf miner and lives inside the leaf tissue. Damage by young larvae is characterized by small mines and holes in the leaves and surface stripping on the underside of leaves. Older larvae are yellowish green to green caterpillars. They are small (about 12 mm long when full grown) compared to other caterpillars on Brassica crops. The larva is wider in the middle and tapering at both ends with two prolegs on the last segment forming a distinctive V-shape at the posterior Updated 15May2013 by J. Otani 1 end (Figure 3). They feed on leaves, flowers, young pods and surface tissues of stems and mature pods. Damaged seeds do not fill properly and the pods are susceptible to early shattering. -
Novel Aspects of Host Tree Resistance to Leafminers
NOVEL ASPECTS OF HOST TREE RESISTANCE TO LEAFMINERS STANLEY H. FAETH Department of Zoology Arizona State University Tempe, AZ 85287 U.S.A. INTRODUCTION At least 10,000 species of leafminers in four orders of insects (Lepidoptera, Diptera, Coleoptera, and Hymenoptera) are found worldwide. The common feature of all leafminers is that larvae feed within leaves for at least some larval stages. Larvae of facultative mining species feed internally but also externally as free-feeders, usually in later larval instars. Larvae of obligate mining species feed exclusively, and may also pupate, within leaves (Hering 1951, Powell 1980). Despite wide interspecific variation in life histories, leafminers are generally more closely associated with their feeding substrates than are free-feeding insects (Mattson et al. 1988). This "intimacy" (sensu Mattson et al. 1988) is the primary factor in directing their evolution and influencing population dynamics. For leafminers, as distinct from most freefeeding insects, selection of feeding substrates is determined solely by female oviposition choice, at least for obligate leafminers. Eggs may be cemented to the surface or embedded in the leaf, so adult females determine feeding sites not only among plants but also within leaves. For facultative leafminers, female oviposition choice determines larval feeding sites for at least some larval instars, and female choice generally plays a much larger role in larval feeding sites than it does for most external feeding insects. Confinement to a single leaf means that larvae cannot behaviorally escape deteriorating abiotic or biotic conditions associated with their substrates as agile insect larvae can, though a few species can mine more than one leaf by exiting the mine or mining through the petiole to adjacent leaves. -
Characteristics of Parasitism of Diamondback Moth by Oomyzus Sokolowksii (Hymenoptera: Eulophidae)
Characteristics of parasitism of diamondback moth by Oomyzus sokolowksii (Hymenoptera: Eulophidae) N. S. Talekar Asian Vegetable Research and Development Center, Shanhua, Tainan 741, Taiwan, ROC Abstract Laboratory, greenhouse and field studies were conducted on Oomyzus sokolowskii Kurdjumov, a parasite of diamondback moth, Plutella xylostella (L.), to judge its suitability for introduction in the field to control the plutellid. Oomyzus sokolowskii preferred the third and fourth instar diamondback moth larvae over fresh pupae for parasitization. It is thus a larval parasite. Within the range of 10 °C to 35 °C, the higher the temperature the higher was the parasitism rate. High parasitism at temperatures of 30 °C and 35 °C indicates that this insect is suitable for introduction in the tropical lowlands. In a no-choice test where only fresh pupae of Cotesia plutellae Kurdjumov (another potentially competing larval parasite of diamondback moth) were offered, O. sokolowskii failed to parasitize the pupae. In a choice test where the fourth instar diamondback moth larvae and fresh C. plutellae pupae were offered, O. sokolowskii parasitized only diamondback moth larvae. This parasite, therefore, is not a hyperparasite of diamondback moth. When C. plutellae-oviposited diamondback moth larvae were offered at intervals for parasitism by O. sokolowskii, it parasitized only freshly oviposited host larvae. The longer the period that elapsed after C. plutellae oviposition of diamondback moth larvae, the lesser was the parasitism of these larvae by O. sokolowskii. In a field cage study, as the diamondback moth population increased, the parasitism of the pest by the eulophid increased, parasitism by C. plutellae, however, decreased. -
Evaluation of Insecticide Chemistries Against the Leek Moth (Lepidoptera: Acrolepiidae), a New Pest in North America Author(S): Daniel L
Evaluation of Insecticide Chemistries Against the Leek Moth (Lepidoptera: Acrolepiidae), a New Pest in North America Author(s): Daniel L. Olmstead and Anthony M. Shelton Source: Florida Entomologist, 95(4):1127-1131. 2012. Published By: Florida Entomological Society URL: http://www.bioone.org/doi/full/10.1653/024.095.0443 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. Olmstead & Shelton: Chemical Control of the Leek Moth 1127 EVALUATION OF INSECTICIDE CHEMISTRIES AGAINST THE LEEK MOTH (LEPIDOPTERA: ACROLEPIIDAE), A NEW PEST IN NORTH AMERICA DANIEL L. OLMSTEAD* AND ANTHONY M. SHELTON New York State Agricultural Experiment Station, Department of Entomology, Cornell University, 630 West North Street, Geneva, NY 14456, USA *Corresponding author; E-mail: [email protected] Abstract The leek moth, Acrolepiopsis assectella (Zeller), is a newly introduced micro-lepidopteran pest in North America that attacks Allium crops, including onion, leek, and garlic. -
Combating Insecticide Resistance in Major UK Pests: Modelling Section
Rothamsted Research where knowledge grows Combating insecticide resistance in major UK pests: modelling section Joe Helps, Frank van den Bosch, Neil Paveley Start: 1/1/2013 End: 31/7/2016 Project aim • Key questions: Are mixtures beneficial? First need to understand what is the effect of dose on resistance? 1. Build a model of insecticide resistance 2. Explore various measures relating to both: Providing effective control of populations Delaying build up of resistance Insects in the UK Generations per year • Peach-potato aphid Multiple Single • Potato aphid • Grain aphid • Pea aphid • Rose-grain aphid • Currant-lettuce aphid Asexual • Glasshouse whitefly • Two-spotted spider mite • Western flower thrips • Diamondback moth • Leaf miner • Pollen beetle • Cabbage stem flea beetle Asexual / Sexual Asexual • Wheat bulb fly • Orange wheat blossom midge • Pea moth • Codling moth • Pea and bean weevil Sexual Model introduction Insecticide Overwintering insects Maturation Immigration (Susceptible adults) Larvae Adults SS SR RR SS SR RR Birth Damage: • Feeding • Virus transmission • Contamination Crop Model introduction Insecticide Maturation 2 0.99 SS SR 1 RR 0.9 Larvae Adults Logit mortality 0 0.5 Absolute mortality SS SR RR SS SR RR 0.1 -1 Birth -2 0.01 -3 -2 -1 0 1 2 3 Dose (log10) Crop Simulations Grain aphid Pollen beetle 30 50 Data Data Simulation Adults 25 Larvae 40 20 30 Insects per plant per Insects 15 Number of aphids per tille aphids per of Number 20 10 10 5 0 0 0 10 20 30 40 50 60 0 10 20 30 40 50 60 Time (days) Time (days) Data from Skirvin, D.J., Perry, J.N. -
Can We Save Our Horse Chestnut Trees?
Students of La Sainte Union School Milan Zubrik, Forest Research Institute - Slovakia, Bugwood.org Can we save our horse chestnut trees? orse chestnut trees were planted in parks Food web and village greens for their attractive The horse chestnut leaf (producer) is consumed Key words shape and beautiful flowers. We noticed H by the horse chestnut moth larvae (primary invasive species there was extensive early browning of the trees in consumer), which in turn is predated by the blue our school grounds, which we found was caused tit (secondary consumer). Competing with the blue food web by the horse-chestnut leaf-miner, Cameraria ohridella tits are a number of parasitoid wasps. A parasitoid (see CATALYST Volume 25 issue 4, April 2015). Both insect control is an animal that lives inside its host (like a the horse chestnut tree and the Cameraria ohridella parasite), but always kills its host (like a predator parasitoid moth are invasive species but we consider the does, but unlike parasites). The parasitoid wasp moths to be pests because they harm the trees that has a long ovipositor which she uses to insert a we chose to plant. single egg through the leaf cuticle into the larva of We investigated several possibilities of control: the moth. The wasp larva feeds within the moth natural predators (parasitoid wasp and blue tit); larva, eventually killing it. burning or burying fallen leaves in autumn to By counting the number of the leaf miners in a destroy the overwintering pupae; pheromone traps small section of the tree and then scaling up, we that attract and kill male moths. -
Leafmining Insects— Characteristics and Control Whitney S
Leafmining insects— characteristics and control Whitney S. Cranshaw, David A. Leatherman and James R. Feucht1 COLORADO STATE UNIVERSITY COOPERATIVE EXTENSION no. 5.548 Leafminers rarely are abundant enough to be injurious to the plants they infest. However, leaf- miner injury often is conspicuous and can make Quick Facts plants unattractive. Leafy vegetables, such as Leafminers develop and live within leaves spinach, swiss chard or beets, often are consi- of plants and injure the leaves by feed- dered more heavily injured by leafminers since ing on the soft interior tissues. edible parts are directly damaged. On woody Broadly categorized by the shape of "mines" plants, certain leafminers, such as the blackmine produced by their feeding, leafminers blotch leafminer of cottonwood, are a chronic and include many different insects. severe problem in parts of Colorado. Leafminers rarely are abundant enough to be injurious to the plants they infest. The more common leafminers in Colorado Colorado Leafminers are: spinach leafminer, cottonwood Dozens of leafminers occur in Colorado. Among blackmine blotch leafminer, lilac leaf- the more common are: miner, birch leafminer and ponderosa Spinach leafminer: This is a small fry larva pine needle miner. commonly found infesting spinach, swiss chard, beets and lambsquarters. Several generations occur during the year, but are particularly com- mon during the growing season's cooler months. Cottonwood blackmine blotch leafminer: This beetle larva produces an unusually dark and dis- tinctive blotch leafmine. The adult yellow and black beetle can be found chewing and skeletoniz- ing small areas in the exterior leaf surface from late June through July. Eggs also are laid during Leafminers are insects that develop and live this period, and later the larvae initiate mines. -
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.