Insects-Understanding Helicoverpa Ecology and Biology
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Old World Bollworm Management Program Puerto Rico Environmental Assessment, September 2015
United States Department of Agriculture Old World Bollworm Marketing and Regulatory Management Program Programs Animal and Plant Health Inspection Service Puerto Rico Environmental Assessment September 2015 Old World Bollworm Managment Program Puerto Rico Environmental Assessment September 2015 Agency Contact: Eileen Smith Pest Detection and Emergency Programs Plant Protection and Quarantine Animal and Plant Health Inspection Service U.S. Department of Agriculture 4700 River Road, Unit 134 Riverdale, MD 20737 Non-Discrimination Policy The U.S. Department of Agriculture (USDA) prohibits discrimination against its customers, employees, and applicants for employment on the bases of race, color, national origin, age, disability, sex, gender identity, religion, reprisal, and where applicable, political beliefs, marital status, familial or parental status, sexual orientation, or all or part of an individual's income is derived from any public assistance program, or protected genetic information in employment or in any program or activity conducted or funded by the Department. (Not all prohibited bases will apply to all programs and/or employment activities.) To File an Employment Complaint If you wish to file an employment complaint, you must contact your agency's EEO Counselor (PDF) within 45 days of the date of the alleged discriminatory act, event, or in the case of a personnel action. Additional information can be found online at http://www.ascr.usda.gov/complaint_filing_file.html. To File a Program Complaint If you wish to file a Civil Rights program complaint of discrimination, complete the USDA Program Discrimination Complaint Form (PDF), found online at http://www.ascr.usda.gov/complaint_filing_cust.html, or at any USDA office, or call (866) 632-9992 to request the form. -
Bt Resistance Implications for Helicoverpa Zea (Lepidoptera
Environmental Entomology, XX(X), 2018, 1–8 doi: 10.1093/ee/nvy142 Forum Forum Bt Resistance Implications for Helicoverpa zea (Lepidoptera: Noctuidae) Insecticide Resistance Downloaded from https://academic.oup.com/ee/advance-article-abstract/doi/10.1093/ee/nvy142/5096937 by guest on 26 October 2018 Management in the United States Dominic D. Reisig1,3 and Ryan Kurtz2 1Department of Entomology and Plant Pathology, North Carolina State University, Vernon G. James Research and Extension Center, 207 Research Station Road, Plymouth, NC 27962, 2Agricultural & Environmental Research, Cotton Incorporated, 6399 Weston Parkway, Cary, NC 27513, and 3Corresponding author, e-mail: [email protected] Subject Editor: Steven Naranjo Received 19 June 2018; Editorial decision 27 August 2018 Abstract Both maize and cotton genetically engineered to express Bt toxins are widely planted and important pest management tools in the United States. Recently, Helicoverpa zea (Boddie) (Lepidoptera: Noctuidae) has developed resistance to two toxin Bt maize and cotton (Cry1A and Cry2A). Hence, growers are transitioning to three toxin Bt cotton and maize that express both Cry toxins and the Vip3Aa toxin. H. zea susceptibility to Vip3Aa is threatened by 1) a lack of availability of non-Bt refuge crop hosts, including a 1–5% annual decline in the number of non-Bt maize hybrids being marketed; 2) the ineffectiveness of three toxin cultivars to function as pyramids in some regions, with resistance to two out of three toxins in the pyramid; and 3) the lack of a high dose Vip3Aa event in cotton and maize. We propose that data should be collected on current Cry-resistant H. -
The Seasonal Abundance and Impact of Predatory Arthropods on Helicoverpa Species in Australian Cotton Fields
The Seasonal Abundance and Impact of Predatory Arthropods on Helicoverpa Species in Australian Cotton Fields by John Newton Stanley B.Rur. Sc. (University of New England) A thesis submitted for the degree of Doctor of Philosophy from the University of New England Department of Agronomy and Soil Science September 1997 Many Thanks to the Following: Associate Professor Peter Gregg, who, as sole supervisor, provided a broad field of opportunities, as well as cotton, for the discovery of entomological things. Thank you for your guidance and support. Mr. Richard Browne, of Auscott Pty. Ltd., and Ben and Dave Coulton, of Coulton Farming Ltd. for allowing me access to their crops and for adjusting their cultural practices to accommodate experimental designs. Particular thanks to Terry Haynes (Senior Agronomist; Auscott Pty. Ltd. Moree) for discussions on pest management and generously supplying assistance at critical times. The taxonomists who identified material for the insect survey. Mr. L. Bauer (Thysanoptera) Dr. A. Calder (Coleoptera) Dr. M. Carver (Homoptera and Trichogrammatidae) Dr. D. H. Colless (Diptera) Dr. M. J. Fletcher (Cicadellidae) Dr. M. R. Gray (Aracnida) Dr. M. B. Malipatil (Hemiptera) Dr. I. D. Naumann (Hymenoptera) Dr. T. R. New (Neuroptera) Dr. T. A. Weir (Coleoptera) The people who provided technical assistance: Holly Ainslie, Dr. Steven Asante, Doreen Beness, Laura Bennett, Samantha Browne, Dr. Mark Coombs, Peter Foreman, Jacqueline Prudon, Sally Schwitzer, Kelly Stanley, Anita Stevenson, Donald Wheatley, and Richard Willis. Dr. Steven Trowell for guidance using serological methods and to Dr. Anne Bourne for her statistical significance. Mr. Robert Gregg for accomodating my family at Tyree whilst sampling in Moree. -
Insects Parasitoids: Natural Enemies of Helicoverpa
Queensland the Smart State insects Parasitoids: Natural enemies of helicoverpa Introduction Helicoverpa caterpillars (often called heliothis) are serious pests of many crops in Australia. A range of parasitoid and predatory insects attack helicoverpa. Identifying and conserving these beneficial insects is fundamental to implementing pest management with a reduced reliance on chemical insecticides. This brochure describes the most important parasitoids of helicoverpa in Australian broadacre crops. Parasitoids versus parasites: What’s the difference? Parasitoids kill their hosts; parasites (such Figure 1. Netelia producta is one of the as lice and fleas) do not. All the insects most commonly encountered parasitoids in this brochure are parasitoids. Despite of helicoverpa. Females lay their eggs onto this difference, the terms parasitoid and caterpillars, and the hatching wasp larva parasite are often used interchangeably, if feeds on its host, eventually killing it. inaccurately. Parasitoids such as Netelia can be important biological control agents of helicoverpa in crops. (Photo: K. Power) All comments about parasitoid abundance in this publication are based on field observations in southern Queensland farming systems. These patterns may not occur in all parts of Australia. About parasitoids What is a parasitoid? How do parasitoids find their A parasitoid is an insect that kills (parasitises) hosts? its host — usually another insect — in Many adult parasitoids find their host by order to complete its lifecycle. In Australia, smell. They can detect the direct odour of helicoverpa are parasitised by many species the host itself, or odours associated with host of wasps and flies. All helicoverpa immature activity, such as plant damage or caterpillar stages are parasitised (that is, egg, caterpillar frass (dung). -
Classical Biological Control of Arthropods in Australia
Classical Biological Contents Control of Arthropods Arthropod index in Australia General index List of targets D.F. Waterhouse D.P.A. Sands CSIRo Entomology Australian Centre for International Agricultural Research Canberra 2001 Back Forward Contents Arthropod index General index List of targets The Australian Centre for International Agricultural Research (ACIAR) was established in June 1982 by an Act of the Australian Parliament. Its primary mandate is to 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 are used this constitutes neither endorsement of nor discrimination against any product by the Centre. ACIAR MONOGRAPH SERIES This peer-reviewed series contains the results of original research supported by ACIAR, or material deemed relevant to ACIAR’s research objectives. The series is distributed internationally, with an emphasis on the Third World. © Australian Centre for International Agricultural Research, GPO Box 1571, Canberra ACT 2601, Australia Waterhouse, D.F. and Sands, D.P.A. 2001. Classical biological control of arthropods in Australia. ACIAR Monograph No. 77, 560 pages. ISBN 0 642 45709 3 (print) ISBN 0 642 45710 7 (electronic) Published in association with CSIRO Entomology (Canberra) and CSIRO Publishing (Melbourne) Scientific editing by Dr Mary Webb, Arawang Editorial, Canberra Design and typesetting by ClarusDesign, Canberra Printed by Brown Prior Anderson, Melbourne Cover: An ichneumonid parasitoid Megarhyssa nortoni ovipositing on a larva of sirex wood wasp, Sirex noctilio. Back Forward Contents Arthropod index General index Foreword List of targets WHEN THE CSIR Division of Economic Entomology, now Commonwealth Scientific and Industrial Research Organisation (CSIRO) Entomology, was established in 1928, classical biological control was given as one of its core activities. -
Data Sheet on Helicoverpa
EPPO quarantine pest Prepared by CABI and EPPO for the EU under Contract 90/399003 Data Sheets on Quarantine Pests Helicoverpa zea IDENTITY Name: Helicoverpa zea (Boddie) Synonyms: Heliothis zea (Boddie) Bombyx obsoleta Fab. Phalaena zea (Boddie) Heliothis umbrosus Grote Taxonomic position: Insecta: Lepidoptera: Noctuidae Common names: American bollworm, corn earworm, tomato fruitworm, New World bollworm (English) Chenille des épis du maïs (French) Amerikanischer Baumwollkapselwurm (German) Notes on taxonomy and nomenclature: The taxonomic situation is complicated and presents several problems. Hardwick (1965) reviewed the New World corn earworm species complex and the Old World African bollworm (Noctuidae), most of which had previously been referred to as a single species (Heliothis armigera or H. obsoleta), and pointed out that there was a complex of species and subspecies involved. Specifically he proposed that the New World H. zea (first used in 1955) was distinct from the Old World H. armigera on the basis of male and female genitalia. And he described the new genus Helicoverpa to include these important pest species, Some 80 or more species were formerly placed in Heliothis (sensu lato) and Hardwick referred 17 species (including 11 new species) to Helicoverpa on the basis of differences in both male and female genitalia. Within this new genus the zea group contains eight species, and the armigera group two species with three subspecies. See also Hardwick (1970). Because the old name of Heliothis for the pest species (four major pest species and three minor) is so well established in the literature, and since dissection of genitalia is required for identification, there has been resistance to the name change (e.g. -
Insects by Cindy Grigg
Insects By Cindy Grigg 1 Like you, insects are alive. Both people and insects are animals. Insects are different from most other animals. Let's read to find out how they are different. 2 Insects are invertebrate animals. That means they have no backbone. Insects are the largest group of animals on Earth. In fact, about half of all animals that scientists know are insects! 3 Insects have three main body parts. They are the head, the thorax, and the abdomen. They have six legs. Many adult insects also have wings. The wings and legs are attached to the thorax. 4 Some invertebrate animals look like insects, but they are not. Spiders and scorpions, for example, are commonly confused with insects. Spiders and scorpions are not insects because they have eight legs, not six. They also have only two body segments instead of three. 5 Most insects lay eggs. Some young insects look like their parents. Other young insects, such as caterpillars, look very different from their parents. 6 All the stages in the life of an animal make up the animal's life cycle. Butterflies have a four-stage life cycle. Butterflies often lay eggs on leaves the insects can eat after they hatch. The egg is the first stage of the butterfly's life cycle. 7 When the egg hatches, a larva comes out of the egg. We often call the larva a caterpillar. This is the second stage. The caterpillar looks very different from the adult butterfly. The larva eats the leaves and grows very quickly. 8 After the larva grows big enough, it makes a hard covering for itself. -
Autographa Gamma
1 Table of Contents Table of Contents Authors, Reviewers, Draft Log 4 Introduction to the Reference 6 Soybean Background 11 Arthropods 14 Primary Pests of Soybean (Full Pest Datasheet) 14 Adoretus sinicus ............................................................................................................. 14 Autographa gamma ....................................................................................................... 26 Chrysodeixis chalcites ................................................................................................... 36 Cydia fabivora ................................................................................................................. 49 Diabrotica speciosa ........................................................................................................ 55 Helicoverpa armigera..................................................................................................... 65 Leguminivora glycinivorella .......................................................................................... 80 Mamestra brassicae....................................................................................................... 85 Spodoptera littoralis ....................................................................................................... 94 Spodoptera litura .......................................................................................................... 106 Secondary Pests of Soybean (Truncated Pest Datasheet) 118 Adoxophyes orana ...................................................................................................... -
Thrips Page 1
Insect Order Identification Home Thysanoptera–Thrips Page 1 Life Cycle--Intermediate metamorphosis (between complete and simple). Winged adults mate and lay eggs. Larvae (nymphs) look similar to adults in form and shape but lack both wings and wingbuds. Larvae eat, molt, and grow larger until entering a non-feeding larval stage (pupa) in which wings form and a color change may occur but the form remains essentially the same. Some species have one or more non-feeding pre-pupal stages. The emerging winged adult looks similar to the larva. Adults--Minuscule insects (usually 1/16 inch or less). Magnification may be needed to see them. Adults are usually dark-colored, yellow to black. Shape elongated and slender. Two pairs of wings are long and narrow and held over the body. Edges of both forewings and hindwings are fringed or feathery. (Click images to enlarge.) Black dots are Feathery-edged wings Wings tube-tailed thrips long & narrow Brown dots are mixture of adults, larvae & damage One of the black dots above Feathery-edged One of the wings brown dots above Insect Order Identification Home Thysanoptera–Thrips Page 2 Eggs--Some female thrips lay their eggs in tiny slits cut into the surface of leaves, fruits, flowers, and stems. Indoors, the eggs can be laid any time of year and hatch within a few days in warm, indoor conditions. In some species the fertilized eggs are all parthenogenic females (able to reproduce without sex) and the unfertilized are males. (Click images to enlarge.) Thrips eggs Close-up of eggs Larvae (Nymphs)--Look similar to adults but entirely wingless and usually pale-colored, white to cream or pale green. -
Molecular Characterization of Fall Armyworm (Spodoptera Frugiperda) Resistant to Vip3aa20 Protein Expressed in Corn
Molecular Characterization of Fall Armyworm (Spodoptera frugiperda) Resistant to Vip3Aa20 Protein Expressed in Corn Dissertation Presented in partial fulfillment of the requirements for the degree of doctor of philosophy in the Graduate School of The Ohio State University Julio Cesar Fatoretto, B. Sc. Graduate Program in Translational Plant Science The Ohio State University 2017 Dissertation Committee: Andrew P. Michel, Advisor Marcio C. Silva Filho Thomas Mitchell Fernando Consoli Copyright by Julio Cesar Fatoretto 2017 Abstract Transgenic plants containing genes from Bacillus thuringiensis have been used as an alternative to chemical insecticides for insect pest control. The vegetative insecticidal proteins (Vip) secreted during the vegetative growth phase of bacteria are considered a second generation of insecticidal proteins since they do not share any structural or sequence homology with previously used crystal proteins (Cry) as well as having a wide insecticidal spectrum. One of the target pests for this protein is the fall armyworm (FAW) (Spodoptera frugiperda), the most important corn pest in South America. Previously it has been controlled by insecticides and corn expressing Cry proteins, but has rapidly evolved resistance to many control practices and remains a top concern for sustainable biotechnology control efforts. Thus, resistance characterization involving mode of action and genetics of resistance can help with Insect Resistance Management strategies, and improve the durability of control. In this dissertation, using selected FAW population resistant to Vip3Aa20 Bt protein (Vip-R1and Vip-R2) we generated comparative proteomic and transcriptomic data among resistant and susceptible colonies. In the chapter 2, we bring FAW biology/ecology and Brazilian agriculture landscape data to support the high adaptive potential of this pest to genetically modified corn expressing Bt Cry proteins in Brazil. -
Colorado Potato Beetle.Pub
CORNELL COOPERATIVE EXTENSION OF ONEIDA COUNTY 121 Second Street Oriskany, NY 13424-9799 (315) 736-3394 or (315) 337-2531 FAX: (315) 736-2580 Colorado Potato Beetle Leptinotarsa decemlineata Description: The Colorado potato beetle was first described in 1824 from the upper Missouri River Valley where it fed on a weed called buffalo bur or sand bur, but when early settlers first began to plant potatoes, the beetles discovered the new food plant and liked it. Adult Colorado Potato Beetle Colorado Potato Beetle larva Injury: Larvae and adults feed on the foliage of potato, eggplant, tomatoes and peppers. They may reach large numbers and eat all the foliage from the plant as well as spoil the fruit by eating into it. They are especially de- structive to small plantings. Life History: Adult beetles come out of winter hibernation in mid-May on Long Island and a week or ten days later in central New York just before the early-planted potatoes are up. Clusters of 20 or more eggs are laid on the underside of the leaves soon after the beetles emerge. The eggs hatch in seven to ten days. The larvae feed on the foliage, grow rapidly and complete their development in 18 to 21 days. The full-grown larva burrows into the ground and changes to the pupa or resting stage. After seven to ten days, the adult beetle emerges from the pupa, crawls up out of the ground, and after a short period of waiting, lays eggs for the second generation. Management: In the past several years, the Colorado potato beetle has become increasingly difficult to control because it has developed resistance to many commonly used chemical insecticides. -
Aspects of the Ecology of Helicoverpa Punctigera – What Has Changed?
Chapter 1: Aspects of the ecology of Helicoverpa punctigera – what has changed? 1.1 Background The genus Helicoverpa is part of the noctuid family of moths and has a worldwide range of species, which include Helicoverpa armigera (Hübner, 1805), Helicoverpa assulta (Guenée, 1852) Helicoverpa atacamae (Hardwick, 1965) Helicoverpa fletcheri (Hardwick, 1965), Helicoverpa gelotopoeon (Dyar, 1921), Helicoverpa hardwicki (Matthews, 1999), Helicoverpa hawaiiensis (Quaintance & Brues, 1905), Helicoverpa helenae (Hardwick, 1965), Helicoverpa pallida (Hardwick, 1965), Helicoverpa prepodes (Common, 1985), Helicoverpa punctigera (Wallengren, 1860), Helicoverpa titicaca (Hardwick, 1965), Helicoverpa toddi (Hardwick, 1965) and Helicoverpa zea (Boddie, 1850). As cotton bollworms and legume pod borers, larvae of Helicoverpa spp. are among the most significant crop pests worldwide (Fitt and Cotter, 2005). There are two species of the genus Helicoverpa that are agriculturally significant in Australia, the cotton bollworm Helicoverpa armigera and the native budworm Helicoverpa punctigera. The cosmopolitan H. armigera and the Australian native H. punctigera are the most important pests of field crops in Australia (Zalucki et al., 1986). Although the two species are closely related and share similar colouration and body sizes, each species has differing host-plant ranges, seasonal abundances and geographic ranges (Zalucki et al., 1986, Fitt and Cotter, 2005). Helicoverpa armigera achieves 4-5 generations per season over most of Queensland and much of Northern New South Wales (Fitt and Daly, 1990). The diverse host range of H. armigera means that at any one time there may be a mosaic of subpopulations linked by adult migration, each with different mortality rates and fitness effects imposed by their environment (Dillon et al., 1996).