California's Worst Garden Insect Pests and How to Manage Them
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(Cydia Pomonella L.) and Woolly Apple Aphid, (Eriosoma Lanigerum) on Apple (Malus Domestica L
International Journal of Entomology Research International Journal of Entomology Research ISSN: 2455-4758; Impact Factor: RJIF 5.24 Received: 17-05-2020; Accepted: 19-05-2020; Published: 08-06-2020 www.entomologyjournals.com Volume 5; Issue 3; 2020; Page No. 156-160 Population trend of codling moth (Cydia pomonella l.) And woolly apple aphid, (Eriosoma lanigerum) on apple (Malus domestica L. Borkh) fruit tree orchard Muhammad Umer1, Noor Muhammad2*, Nisar Uddin3, Muhammad Khalil Ullah Khan4, Shariat Ullah5, Niaz Ali6 1 Department of Plant Protection, The Agriculture University of Peshawar, Peshawar, KP, Pakistan 2, 4 Department of Pomology, College of Horticultural Hebei Agricultural University, Baoding, Hebei China 3, 5 Department of Botany University of Malakand, KP, Pakistan 6 Department of Botany Hazara University, KP, Pakistan Abstract The population trends of Cydia pomonella L. and Eriosoma lanigerum were studied on apple fruit orchard. These two pests caused serious losses in district Mastung, Balochistan Province, Pakistan. The results of weekly mean population dynamics showed that the mean population of Cydia pomonella L. on each apple fruit tree varied. For the first week it varied from 0.0 to 8.0 in which the maximum attack of the Codling moth was 8.0 for treatment (T) 6. In the same way the highest attack in the week; first, second, third, fourth, to tenth was 3.5, 8.0, 4.5, 3.0, 3.0, 4.0, 4.5, 4.5, and 4.5 respectively. While the mean population dynamics of (Eriosoma lanigerum) ranged from 0.0 to 4.0 in first week. Among the population maximum invasion of Woolly apple aphid for week first, second, third, fourth, to tenth was 4.0, 3.0, 3.0, 6.0, 6.0, 3, 4, 3, 4 and 6 respectively. -
Aphis Fabae Scop.) to Field Beans ( Vicia Faba L.
ANALYSIS OF THE DAMAGE CAUSED BY THE BLACK BEAN APHID ( APHIS FABAE SCOP.) TO FIELD BEANS ( VICIA FABA L.) BY JESUS ANTONIO SALAZAR, ING. AGR. ( VENEZUELA ) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN THE UNIVERSITY OF LONDON OCTOBER 1976 IMPERIAL COLLEGE FIELD STATION, SILWOOD PARK, SUNNINGHILL, ASCOT, BERKSHIRE. 2 ABSTRACT The concept of the economic threshold and its importance in pest management programmes is analysed in Chapter I. The significance of plant responses or compensation in the insect-injury-yield relationship is also discussed. The amount of damage in terms of yield loss that results from aphid attack, is analysed by comparing the different components of yield in infested and uninfested plants. In the former, plants were infested at different stages of plant development. The results showed that seed weights, pod numbers and seed numbers in plants infested before the flowering period were significantly less than in plants infested during or after the period of flower setting. The growth pattern and growth analysis in infested and uninfested plants have shown that the rate of leaf production and dry matter production were also more affected when the infestations occurred at early stages of plant development. When field beans were infested during the flowering period and afterwards, the aphid feeding did not affect the rate of leaf and dry matter production. There is some evidence that the rate of leaf area production may increase following moderate aphid attack during this period. The relationship between timing of aphid migration from the wintering host and the stage of plant development are shown to be of considerable significance in determining the economic threshold for A. -
(Pentatomidae) DISSERTATION Presented
Genome Evolution During Development of Symbiosis in Extracellular Mutualists of Stink Bugs (Pentatomidae) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Alejandro Otero-Bravo Graduate Program in Evolution, Ecology and Organismal Biology The Ohio State University 2020 Dissertation Committee: Zakee L. Sabree, Advisor Rachelle Adams Norman Johnson Laura Kubatko Copyrighted by Alejandro Otero-Bravo 2020 Abstract Nutritional symbioses between bacteria and insects are prevalent, diverse, and have allowed insects to expand their feeding strategies and niches. It has been well characterized that long-term insect-bacterial mutualisms cause genome reduction resulting in extremely small genomes, some even approaching sizes more similar to organelles than bacteria. While several symbioses have been described, each provides a limited view of a single or few stages of the process of reduction and the minority of these are of extracellular symbionts. This dissertation aims to address the knowledge gap in the genome evolution of extracellular insect symbionts using the stink bug – Pantoea system. Specifically, how do these symbionts genomes evolve and differ from their free- living or intracellular counterparts? In the introduction, we review the literature on extracellular symbionts of stink bugs and explore the characteristics of this system that make it valuable for the study of symbiosis. We find that stink bug symbiont genomes are very valuable for the study of genome evolution due not only to their biphasic lifestyle, but also to the degree of coevolution with their hosts. i In Chapter 1 we investigate one of the traits associated with genome reduction, high mutation rates, for Candidatus ‘Pantoea carbekii’ the symbiont of the economically important pest insect Halyomorpha halys, the brown marmorated stink bug, and evaluate its potential for elucidating host distribution, an analysis which has been successfully used with other intracellular symbionts. -
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. -
Kansas Insect Newsletter
Kansas Insect Newsletter For Agribusinesses, Applicators, Consultants and Extension Personnel Department of Entomology 123 West Waters Hall K-State Research and Extension Manhattan, Kansas 66506 785-532-5891 http://www.entomology.ksu.edu/extension __________________________________________________________________________________________________ April 13, 2012 No. 6 Aphids on Roses Aphids are “out-and-about” on a variety of plants including chrysanthemum, oak, and rose. Although roses are one of the most beautiful plants grown in landscapes and gardens they are susceptible to attack from a multitude of arthropod (insect and mite) pests. In fact, roses may be attacked by different aphid species such as the potato aphid (Macrosiphum euphorbiae) and the cotton aphid (Aphis gossypii); however, the predominant species that feeds on cultivated roses is the rose aphid (Macrosiphum rosae). Rose aphids are soft-bodied, pear-shaped insects approximately 1/4 inches long. They may vary in color from green to pink to red. There are two tubes, called cornicles that protrude out from the end of the abdomen. Rose aphids overwinter as eggs on rose canes. Rose aphids typically start feeding on roses in early spring (RIGHT NOW!) as the new flush of growth emerges. They cluster on leaves, stems, and developing buds. Rose aphids feed on plant fluids (e.g., phloem) with their piercing-sucking mouthparts, and tend to congregate in large numbers, feeding on terminal growth such as leaves and developing flower buds, and on leaf undersides. Their feeding causes leaves to curl upward and deforms flower buds. Flower buds may abort or fall prematurely before opening. In addition, rose aphids produce copious amounts of honeydew, which is a clear, sticky liquid exudate produced during feeding. -
Correlation of Stylet Activities by the Glassy-Winged Sharpshooter, Homalodisca Coagulata (Say), with Electrical Penetration Graph (EPG) Waveforms
ARTICLE IN PRESS Journal of Insect Physiology 52 (2006) 327–337 www.elsevier.com/locate/jinsphys Correlation of stylet activities by the glassy-winged sharpshooter, Homalodisca coagulata (Say), with electrical penetration graph (EPG) waveforms P. Houston Joosta, Elaine A. Backusb,Ã, David Morganc, Fengming Yand aDepartment of Entomology, University of Riverside, Riverside, CA 92521, USA bUSDA-ARS Crop Diseases, Pests and Genetics Research Unit, San Joaquin Valley Agricultural Sciences Center, 9611 South Riverbend Ave, Parlier, CA 93648, USA cCalifornia Department of Food and Agriculture, Mt. Rubidoux Field Station, 4500 Glenwood Dr., Bldg. E, Riverside, CA 92501, USA dCollege of Life Sciences, Peking Univerisity, Beijing, China Received 5 May 2005; received in revised form 29 November 2005; accepted 29 November 2005 Abstract Glassy-winged sharpshooter, Homalodisca coagulata (Say), is an efficient vector of Xylella fastidiosa (Xf), the causal bacterium of Pierce’s disease, and leaf scorch in almond and oleander. Acquisition and inoculation of Xf occur sometime during the process of stylet penetration into the plant. That process is most rigorously studied via electrical penetration graph (EPG) monitoring of insect feeding. This study provides part of the crucial biological meanings that define the waveforms of each new insect species recorded by EPG. By synchronizing AC EPG waveforms with high-magnification video of H. coagulata stylet penetration in artifical diet, we correlated stylet activities with three previously described EPG pathway waveforms, A1, B1 and B2, as well as one ingestion waveform, C. Waveform A1 occured at the beginning of stylet penetration. This waveform was correlated with salivary sheath trunk formation, repetitive stylet movements involving retraction of both maxillary stylets and one mandibular stylet, extension of the stylet fascicle, and the fluttering-like movements of the maxillary stylet tips. -
Differences in the Sugar Composition of the Honeydew of Polyphagous
NOTE Eur. J. Entomol. 108: 705–709, 2011 http://www.eje.cz/scripts/viewabstract.php?abstract=1671 ISSN 1210-5759 (print), 1802-8829 (online) Differences in the sugar composition of the honeydew of polyphagous brown soft scale Coccus hesperidum (Hemiptera: Sternorrhyncha: Coccoidea) feeding on various host plants KATARZYNA GOLAN 1 and AGNIESZKA NAJDA2 1Department of Entomology, University of Life Sciences in Lublin, LeszczyĔskiego 7, 20-069 Lublin, Poland; e-mail: [email protected] 2 Department of Vegetable and Medicinal Plants, University of Life Sciences in Lublin, LeszczyĔskiego 58, 20-068 Lublin, Poland Key words. Coccoidea, Coccus hesperidum, brown scale insects, honeydew, host plants, soft scale, sugar composition Abstract. Plant chemical composition is an important determinant of host plant-insect interactions. For many insects sugars are the main factors determining the acceptability of a plant. This study investigated changes in plant chemical composition and differences in sugar composition of different host plants induced by the feeding of Coccus hesperidum L. (Hemiptera: Sternorrhyncha: Coccoi- dea). Present in plant extracts and honeydew there were three monosaccharide sugars: glucose, fructose and arabinose, and one disaccharide – sucrose. Arabinose was only found in extracts of Ficus benjamina plants. The sugar content of the honeydew was greater than in the extracts of control plants and lower than that in the extracts of infested plants. The honeydew collected from C. hesperidum feeding on the three plant species differed significantly in sugar content. Extracts of coccid infested plants of the three species used in this study contained more sugar than the un-infested control plants. The results show that honeydew composition of scale insects differ and the differences reflect the chemical composition of the host plants. -
Twenty-Five Pests You Don't Want in Your Garden
Twenty-five Pests You Don’t Want in Your Garden Prepared by the PA IPM Program J. Kenneth Long, Jr. PA IPM Program Assistant (717) 772-5227 [email protected] Pest Pest Sheet Aphid 1 Asparagus Beetle 2 Bean Leaf Beetle 3 Cabbage Looper 4 Cabbage Maggot 5 Colorado Potato Beetle 6 Corn Earworm (Tomato Fruitworm) 7 Cutworm 8 Diamondback Moth 9 European Corn Borer 10 Flea Beetle 11 Imported Cabbageworm 12 Japanese Beetle 13 Mexican Bean Beetle 14 Northern Corn Rootworm 15 Potato Leafhopper 16 Slug 17 Spotted Cucumber Beetle (Southern Corn Rootworm) 18 Squash Bug 19 Squash Vine Borer 20 Stink Bug 21 Striped Cucumber Beetle 22 Tarnished Plant Bug 23 Tomato Hornworm 24 Wireworm 25 PA IPM Program Pest Sheet 1 Aphids Many species (Homoptera: Aphididae) (Origin: Native) Insect Description: 1 Adults: About /8” long; soft-bodied; light to dark green; may be winged or wingless. Cornicles, paired tubular structures on abdomen, are helpful in identification. Nymph: Daughters are born alive contain- ing partly formed daughters inside their bodies. (See life history below). Soybean Aphids Eggs: Laid in protected places only near the end of the growing season. Primary Host: Many vegetable crops. Life History: Females lay eggs near the end Damage: Adults and immatures suck sap from of the growing season in protected places on plants, reducing vigor and growth of plant. host plants. In spring, plump “stem Produce “honeydew” (sticky liquid) on which a mothers” emerge from these eggs, and give black fungus can grow. live birth to daughters, and theygive birth Management: Hide under leaves. -
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. -
Onion Thrips (Thrips Tabaci)
Published by Utah State University Extension and Utah Plant Pest Diagnostic Laboratory ENT-117-08PR March 2008 Onion Thrips (Thrips tabaci) Diane G. Alston, Entomologist • Daniel Drost, Vegetable Specialist What You Should Know • Onion thrips are the most injurious insect pest to onions in Utah. • Immature and adult thrips prefer to feed on young leaves in the inner neck of plants. • Moderate to severe thrips feeding causes reduced bulb size. • Insecticides are a major tool for their control, but thrips are prone to develop resistance. • Long-term, sustainable management of thrips includes crop cultural practices, onion varietal resistance, biological control, and insecticide resistance management. nion thrips, thrips Thrips tabaci (Order Thysanoptera, Thysanoptera OFamily Thripidae), is a key insect pest in most onion production regions of the world. Immature and adult thrips feed with a punch-and-suck behavior that removes leaf chlorophyll causing white to silver patches and Fig. 2. Adult onion thrips have fringed or hairy wings 2 streaks (Fig. 1). Thrips populations increase rapidly under and 7-segmented antennae. hot, arid conditions and can lead to economic crop unsustainable management. Life history characteristics loss. The early bulb enlargement stage of onion growth of onion thrips that enhance their pest status include is the most sensitive to thrips feeding. Insecticides have a short generation time, high reproductive potential, been the primary tactic for their management; however, asexual reproduction by females (parthenogenesis), repeated applications often lead to resistance in the and occurrence of protected, non-feeding life stages. thrips population, suppression of natural enemies, and Recent research has shown that the majority of onion thrips on a plant are in the non-feeding egg stage (60- 75% of total population on an onion plant during late June to August), and thus, not exposed to insecticides and other suppressive tactics. -
False Codling Moth Thaumatotibia Leucotreta
Stone Fruit Commodity-Based Pest Survey False Codling Moth Thaumatotibia leucotreta Introduction False codling moth (Figure 1) is a significant pest because of its potential economic impact on many crops, including stone fruit, avocado, citrus, corn, cotton, and macadamia. It is not currently known to be present in the United States. Biology Depending on conditions, the false codling moth’s life cycle ranges from 30 to 174 days. It can produce from 2 to 10 generations each year, depending on multiple factors including temperature, food availability and quality, and humidity. To attract males, adult females release pheromones at FIGURE 1. Adult false codling moth (Thaumatotibia leucotreta). Photo courtesy of night. After the adults mate, the female deposits eggs on Pest and Diseases Image Library, Bugwood.org. host plants, either in batches or as single eggs. Later, the hatching larvae burrow into the rind of the host plant. Mature larvae spin cocoons and pupate before they emerge as adults. Symptoms False codling moth can attack stone fruit at any stage. Larvae can even develop in hard green fruit prior to application of control measures. Larvae burrow at the stem end into the fruit and cause damage by feeding around the stone. Damaged fruit can become vulnerable to secondary pests such as fungal organisms and scavengers. Peaches can be damaged by larvae beginning up to 6 weeks before harvest. False codling moth can also attack plants unsuitable for larvae development, such as avocado, causing lesions on fruit tissue and diminishing the marketability of fruit. Because false codling moth is an internal feeder, few symptoms are actually displayed by the larvae. -
Thrips Pollination of Mesozoic Gymnosperms
Thrips pollination of Mesozoic gymnosperms Enrique Peñalvera, Conrad C. Labandeirab,c,1, Eduardo Barróna, Xavier Delclòsd, Patricia Nele, André Nele, Paul Tafforeauf, and Carmen Sorianof aMuseo Geominero, Instituto Geológico y Minero de España, Madrid E-28003, Spain; bDepartment of Paleobiology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013; cDepartment of Entomology and Behavior, Ecology, Evolution and Systematics Program, University of Maryland, College Park, MD 20742; dDepartament d’Estratigrafia, Paleontologia i Geociències Marines, Facultat de Geologia, Universitat de Barcelona, E-08071, Spain; eCentre National de la Recherche Scientifique Unité Mixte de Recherche 7205, Entomologie, Muséum National d’Histoire Naturelle, Paris F-75005; Département Sciences de la Vie et Santé, AgroParisTech, Paris F-75231, France; and fEuropean Synchrotron Radiation Facility, Grenoble, F-38000, France Edited by David L. Dilcher, Indiana University, Bloomington, IN, and approved April 10, 2012 (received for review December 13, 2011) Within modern gymnosperms, conifers and Ginkgo are exclusively several to a few hundred pollen grains to flowers (18) or cones wind pollinated whereas many gnetaleans and cycads are insect (Table S1); for example, Cycadothrips chadwicki can deliver up to pollinated. For cycads, thrips are specialized pollinators. We report 5,700 pollen grains per ovule to Macrozamia communis cycad such a specialized pollination mode from Early Cretaceous amber of cones in an afternoon (8). Several species of Cycadothrips are ef- Spain, wherein four female thrips representing a genus and two ficient pollinators of endemic Australian Macrozamia cycads (7, 8, species in the family Melanthripidae were covered by abundant 21). Besides pollination of gnetaleans and cycads, thrips species Cycadopites pollen grains.