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A New Pupillarial Scale Insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in Coastal New South Wales, Australia
Zootaxa 4117 (1): 085–100 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4117.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:5C240849-6842-44B0-AD9F-DFB25038B675 A new pupillarial scale insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in coastal New South Wales, Australia PENNY J. GULLAN1,3 & DOUGLAS J. WILLIAMS2 1Division of Evolution, Ecology & Genetics, Research School of Biology, The Australian National University, Acton, Canberra, A.C.T. 2601, Australia 2The Natural History Museum, Department of Life Sciences (Entomology), London SW7 5BD, UK 3Corresponding author. E-mail: [email protected] Abstract A new scale insect, Aolacoccus angophorae gen. nov. and sp. nov. (Eriococcidae), is described from the bark of Ango- phora (Myrtaceae) growing in the Sydney area of New South Wales, Australia. These insects do not produce honeydew, are not ant-tended and probably feed on cortical parenchyma. The adult female is pupillarial as it is retained within the cuticle of the penultimate (second) instar. The crawlers (mobile first-instar nymphs) emerge via a flap or operculum at the posterior end of the abdomen of the second-instar exuviae. The adult and second-instar females, second-instar male and first-instar nymph, as well as salient features of the apterous adult male, are described and illustrated. The adult female of this new taxon has some morphological similarities to females of the non-pupillarial palm scale Phoenicococcus marlatti Cockerell (Phoenicococcidae), the pupillarial palm scales (Halimococcidae) and some pupillarial genera of armoured scales (Diaspididae), but is related to other Australian Myrtaceae-feeding eriococcids. -
Managing Insects and Related Pests of Roses Bastiaan M
B-6068 6-99 Managing insects and related pests of roses Bastiaan M. Drees, Brent Pemberton and Charles L. Cole* to outbreaks of spider mites. Thus, protecting exas is well known for roses. In the Tyler roses from insects and mites requires continual region, roses are grown commercially in care and substantial knowledge of pests and Tgreenhouses and outdoor nurseries, where management alternatives, including pesticides field-grown cut flowers, potted miniature roses, and their use. bare-root roses for use in landscapes, and potted roses for the garden-center trade are produced. Monitoring and identifying Although several species of roses are native to the state, the rose industry is based primarily on pests and their damage the many exotic rose hybrids available, including Detecting and identifying pests are the first antique and shrub roses, which have fewer pest steps in managing insects attacking roses. Inspect problems. One of the largest antique-rose pro- plants regularly for pests and the injury they ducers in the nation is produce. For example, located near Brenham, check the underside of a Texas. set number of leaves weekly for such pests as Because roses are grown spider mites or aphids. and appreciated primarily Regular inspections can for their aesthetic value, help growers detect the the plants—and particularly arrival of new pests or the blossoms—should be document the abundance relatively free from pest of pests over time. In addi- damage. Rose plants in the tion, monitoring helps landscape need not neces- growers time their sup- sarily be blemish-free, but pression methods and still should be healthy and evaluate their effectiveness add to the plantings’ overall better. -
Coccidology. the Study of Scale Insects (Hemiptera: Sternorrhyncha: Coccoidea)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Ciencia y Tecnología Agropecuaria (E-Journal) Revista Corpoica – Ciencia y Tecnología Agropecuaria (2008) 9(2), 55-61 RevIEW ARTICLE Coccidology. The study of scale insects (Hemiptera: Takumasa Kondo1, Penny J. Gullan2, Douglas J. Williams3 Sternorrhyncha: Coccoidea) Coccidología. El estudio de insectos ABSTRACT escama (Hemiptera: Sternorrhyncha: A brief introduction to the science of coccidology, and a synopsis of the history, Coccoidea) advances and challenges in this field of study are discussed. The changes in coccidology since the publication of the Systema Naturae by Carolus Linnaeus 250 years ago are RESUMEN Se presenta una breve introducción a la briefly reviewed. The economic importance, the phylogenetic relationships and the ciencia de la coccidología y se discute una application of DNA barcoding to scale insect identification are also considered in the sinopsis de la historia, avances y desafíos de discussion section. este campo de estudio. Se hace una breve revisión de los cambios de la coccidología Keywords: Scale, insects, coccidae, DNA, history. desde la publicación de Systema Naturae por Carolus Linnaeus hace 250 años. También se discuten la importancia económica, las INTRODUCTION Sternorrhyncha (Gullan & Martin, 2003). relaciones filogenéticas y la aplicación de These insects are usually less than 5 mm códigos de barras del ADN en la identificación occidology is the branch of in length. Their taxonomy is based mainly de insectos escama. C entomology that deals with the study of on the microscopic cuticular features of hemipterous insects of the superfamily Palabras clave: insectos, escama, coccidae, the adult female. -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
Insects That Feed on Trees and Shrubs
INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture, -
Effects of Thermal Stress on the Brown Planthopper Nilaparvata Lugens
EFFECTS OF THERMAL STRESS ON THE BROWN PLANTHOPPER NILAPARVATA LUGENS (STAL) by JIRANAN PIYAPHONGKUL A thesis submitted to the University of Birmingham For the degree of DOCTOR OF PHILOSOPHY School of Biosciences University of Birmingham February 2013 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. Abstract This study investigated the effects of heat stress on the survival, mobility, acclimation ability, development, reproduction and feeding behaviour of the brown planthopper Nilaparvata lugens. The critical information derived from the heat tolerance studies indicate that some first instar nymphs become immobilized by heat stress at around 30°C and among the more heat tolerant adult stage, no insects were capable of coordinated movement at 38°C. There was no recovery after entry into heat coma, at temperatures around 38°C for nymphs and 42-43°C for adults. At 41.8° and 42.5oC respectively, approximately 50% of nymphs and adults are killed. In a comparison of the acclimation responses between nymphs and adults reared at 23°C and acclimated at either 15 or 30°C, the data indicate that increases in cold tolerance were greater than heat tolerance, and that acclimation over a generation compared with a single life stage increases tolerance across the thermal spectrum. -
Scale – Insect Pests of Vineyards (AWRI Fact Sheet
Fact Sheet VITICULTURE Scale – insect pests of vineyards Please find attached signed T&C form. If Introduction there is anything Scale insects are sap-sucking pests that draw nutrients from plants and excrete a sugary liquid called honeydew. These insects are common in Australian vineyards but typically do not cause enough damage to warrant action to control them. In someelse circumstances that, however, we the can population can reach a threshold where intervention is required to avoid fruit being downgraded or rejected. Because scale insects have not been considered a high priority for viticultural research, knowledge about their biology and ecology in vineyards is limited.to sign or you Scale species need before the The scale species most commonly found in Australian vineyards are grapevine scale (Parthenolecanium persicae) and frosted scale (Parthenolecanium pruinosum), with several other species found rarely. The differences between the main24/12, scale species are subtleplease and they can let be difficult to distinguish. Grapevine scale adults are slightly bigger and oblong in shape, where frosted scale adults are round. Another feature that differentiates the two species is egg colour, with grapevine scale producing pink eggs and frosted scale producing pale yellowme eggs. Inknow. any case, identifying the species is not particularly useful because their life cycles are very similar and control methods are the same. Life cycle Soft scale species complete their life cycle over a 12-month period. As the life cycles are similar for the two main scale species found in Australia, a general model is provided, beginning with the winter period. Updated June 2018 Fact Sheet VITICULTURE Table 1. -
Scale Insects and Mealybugs on Ornamental Plants1
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. ENY-323 Scale Insects and Mealybugs on Ornamental Plants1 Eileen A. Buss and Jay Cee Turner2 Scale insects are the most serious pests of many ornamental plants. There are 13 families of scales in Florida, the most common being armored scales, soft scales, and mealybugs. Scales cause damage by sucking plant fluids from leaves (Figure 1), stems, and sometimes roots. Some species feed on the underside of leaves, which can appear as stippling (small yellow spots) or chlorotic lesions. Heavily infested plants look unhealthy and produce little new growth. Heavy infestations can cause extensive leaf yellowing, premature leaf drop (defoliation), branch dieback, and plant death. Figure 1. Florida wax scales along leaf veins. Credits: Lyle Biology and Behavior Buss, University of Florida and grow. Males of many species develop wings as Life cycles of the various scale species differ adults and fly to locate mates. somewhat, but a generalized life cycle is as follows. The eggs are laid beneath the wax coverings, ovisacs, Armored Scales (Diaspididae) or beneath the adult female (Figure 2). Eggs generally hatch in 1 to 3 weeks. The newly hatched Over 175 species of armored scales occur in nymphs (crawlers) move around the plant until they Florida. They are distinct from other types of scales find a suitable feeding site (Figure 3). Wind may also because they secrete a waxy covering over their transport crawlers to new hosts. Nymphs insert their bodies that is not attached to the body. The scale lives straw-like mouthparts into the plant and begin to feed and feeds under this covering. -
Coleoptera: Coccinellidae): Influence of Subelytral Ultrastructure
Experimental & Applied Acarology, 23 (1999) 97–118 Review Phoresy by Hemisarcoptes (Acari: Hemisarcoptidae) on Chilocorus (Coleoptera: Coccinellidae): influence of subelytral ultrastructure M.A. Houck* Department of Biological Sciences, Texas Tech University, Lubbock, TX 79409–3131, USA (Received 9 January 1997; accepted 17 April 1998) ABSTRACT The non-phoretic stages of mites of the genus Hemisarcoptes are predators of the family Diaspididae. The heteromorphic deutonymph (hypopus) maintains a stenoxenic relationship with beetles of the genus Chilocorus. The mites attach to the subelytral surface of the beetle elytron during transport. There is variation in mite density among species of Chilocorus. Both Hemisarcoptes and Chilocorus have been applied to biological control programmes around the world. The objective of this study was to determine whether subelytral ultrastructure (spine density) plays a role in the evolution of symbiosis between the mite and the beetle. The subelytral surfaces of 19 species of Chilocorus and 16 species of Exochomus were examined. Spine density was determined for five subelytral zones: the anterior pronotal margin, medial central region, caudoventral tip, lateral distal margin and epipleural region. Spine density on the subelytral surface of Chilocorus and Exochomus was inversely correlated with the size of the elytron for all zones except the caudoventral tip. This suggests that an increase in body size resulted in a redistribution of spines and not an addition of spines. The pattern of spine density in Exochomus and Chilocorus follows a single size–density trajectory. The pattern of subelytral ultrastructure is not strictly consistent with either beetle phylogeny or beetle allometry. The absence of spines is not correlated with either beetle genus or size and species of either Chilocorus or Exochomus may be devoid of spines in any zone, irrespective of body size. -
Effects of Ecology, Life History, and Behavior
Effects of Ecology, Life History, and Behavior Edited by Susan Mopper Department of Biology University of Southwestern Louisiana Lafayette, lA Sharon Y. Strauss Section of Evolution and Ecology University of California, Davis Davis, CA CHAPMAN & HALL I (f)p ® INTERNATIONAL THOMSON PUBLISHING Thomson Science New York • Albany • Bonn • Boston • Cincinnati • Detroit London • Madrid • Melbourne o Mexico City o Pacific Grove Cover design: Susan Mopper, Karl Hasenstein, Curtis Tow Graphics Copyright© 1998 by Chapman & Hall Printed in the United States of America Chapman & Hall Chapman & Hall 115 Fifth Avenue 2-6 Boundary Row New York, NY 10003 London SE1 8HN England Thomas Nelson Australia Chapman & Hall GmbH 102 Dodds Street Postfach 100 263 South Melbourne, 3205 D-69442 Weinheim Victoria, Australia Germany International Thomson Editores International Thomson Publishing-Japan Campos Eliseos 385, Piso 7 Hirakawacho-cho Kyowa Building, 3F Col. Polanco 1-2-1 Hirakawacho-cho 11560 Mexico D.F Chiyoda-ku, 102 Tokyo Mexico Japan International Thomson Publishing Asia 221 Henderson Road #05-10 Henderson Building Singapore 0315 All rights reserved. No part of this book covered by the copyright hereon may be reproduced or used in any form or by any means-graphic, electronic, or mechanical, including photocopying, recording, tapin� or information storage and retrieval systems-without the written permission of the publisher. 1 2 3 4 5 6 7 8 9 10 XXX 01 00 99 98 Library of Congress Cataloging-in-Publication Data Genetic structure and local adaptation in natural insect populations: effects of ecology, life history, and behavior I [compiled by] Susan Mopper and Sharon Y. -
Scale Insects (And Spider Mites?)
Quality Time with Scale Insects (and Spider Mites?) Whitney Cranshaw Colorado State University 63rd Annual Shade Tree Conference Topeka, KS January 10, 2018 Scale Insects Order: Hemiptera Families: Diaspididae (armored scales), Coccidae (soft scales), Eriococcidae (Felt scales), others Scale Insect Basics • Scale insects feed on plant fluids using ‘piercing-sucking’ mouthparts – Insect order Hemiptera – Related insects include mealybugs, aphids and whiteflies Willow aphids Longtailed mealybug Scale Insect Basics • Scale insects feed on plant fluids using ‘piercing-sucking’ mouthparts – Insect order Hemiptera – Related insects include mealybugs, aphids and whiteflies • Scale insects produce a protective covering that hides the body Scale Insect Basics • Scale insects feed on plant fluids using ‘piercing-sucking’ mouthparts – Insect order Hemiptera – Related insects include mealybugs, aphids and whiteflies • Scale insects produce a protective covering that hides the body Scale Insect Basics • Scale insects feed on plant fluids using ‘piercing-sucking’ mouthparts – Insect order Hemiptera – Related insects include mealybugs, aphids and whiteflies • Scale insects produce a protective covering that hides the body There are two general types of scale insects: ‘Soft’ Scales Armored Scales Armored Scales Family Diaspididae San Jose scale Obscure scale Oak lecanium European elm scale Soft Scales Families Coccidae, Eriococcidae Pine tortoise scale Cottony maple scale There are two general types of scale insects: ‘Soft’ Scales Armored Scales Armored Scales • Covering completely encloses, but is not attached to, the body • Covering made up primarily of proteins and some waxes • Two primary body forms (elongate, circular) Soft Scales • Covering is attached to body; underside is not covered • Covering made up of waxes • Body forms tend to be elongate-oval, more rounded at maturity Piercing-sucking mouthparts The maxillae are on the inside of the stylet bundle. -
Citrus Mealybug Planococcus Citri (Risso) (Insecta: Hemiptera: Pseudococcidae)1 Harsimran Kaur Gill, Gaurav Goyal, and Jennifer Gillett-Kaufman2
EENY-537 Citrus Mealybug Planococcus citri (Risso) (Insecta: Hemiptera: Pseudococcidae)1 Harsimran Kaur Gill, Gaurav Goyal, and Jennifer Gillett-Kaufman2 Introduction or several weeks. An average of 29 eggs per day is laid by females (Kerns et al. 2001, Meyers 1932). The citrus mealybug is a common pest of citrus primarily in greenhouses and of several ornamental plants in Florida. It has been recognized as a difficult-to-control pest in Europe since 1813 (where it is called the greenhouse mealybug) and in the United States since 1879 (Anonymous 2007). Distribution The pest is a native of Asia but is also found throughout the Americas, Europe, and Oceania. In North America, it is present in both Mexico and United States (Alabama, Arizona, Arkansas, California, Florida, Hawaii, Kansas, Louisiana, Maryland, Massachusetts, Missouri, New Mexico, Ohio, South Carolina, Tennessee, Texas, and Virginia) (CABI/EPPO 1999). Figure 1. Eggs are deposited as white cottony massess called ovisacs. Credits: Lyle Buss, University of Florida. Description and Life History Immatures Eggs Nymphs emerge from the ovisacs and typically settle along Eggs are deposited as white, cottony masses, called ovisacs, midribs and veins on the underside of leaves, young twigs, on the trunk and stems of citrus plants, giving the appear- and fruit buttons. They can also be found where two fruits ance of cotton spread on plants (Figure 1). The glossy, are touching each other (Figure 2) or on leaves clinging light yellow eggs are oval and approximately 0.3 mm long. to fruits. Due to their habit of hiding in crevices, light A female can lay from 300 to 600 eggs in her life period, infestations are easily overlooked.