C Cockroach Biology and Management
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
New Aspects About Supella Longipalpa (Blattaria: Blattellidae)
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Asian Pac J Trop Biomed 2016; 6(12): 1065–1075 1065 HOSTED BY Contents lists available at ScienceDirect Asian Pacific Journal of Tropical Biomedicine journal homepage: www.elsevier.com/locate/apjtb Review article http://dx.doi.org/10.1016/j.apjtb.2016.08.017 New aspects about Supella longipalpa (Blattaria: Blattellidae) Hassan Nasirian* Department of Medical Entomology and Vector Control, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran ARTICLE INFO ABSTRACT Article history: The brown-banded cockroach, Supella longipalpa (Blattaria: Blattellidae) (S. longipalpa), Received 16 Jun 2015 recently has infested the buildings and hospitals in wide areas of Iran, and this review was Received in revised form 3 Jul 2015, prepared to identify current knowledge and knowledge gaps about the brown-banded 2nd revised form 7 Jun, 3rd revised cockroach. Scientific reports and peer-reviewed papers concerning S. longipalpa and form 18 Jul 2016 relevant topics were collected and synthesized with the objective of learning more about Accepted 10 Aug 2016 health-related impacts and possible management of S. longipalpa in Iran. Like the Available online 15 Oct 2016 German cockroach, the brown-banded cockroach is a known vector for food-borne dis- eases and drug resistant bacteria, contaminated by infectious disease agents, involved in human intestinal parasites and is the intermediate host of Trichospirura leptostoma and Keywords: Moniliformis moniliformis. Because its habitat is widespread, distributed throughout Brown-banded cockroach different areas of homes and buildings, it is difficult to control. -
Ancient Roaches Further Exemplify 'No Land Return' in Aquatic Insects
Gondwana Research 68 (2019) 22–33 Contents lists available at ScienceDirect Gondwana Research journal homepage: www.elsevier.com/locate/gr Ancient roaches further exemplify ‘no land return’ in aquatic insects Peter Vršanský a,b,c,d,1, Hemen Sendi e,⁎,1, Danil Aristov d,f,1, Günter Bechly g,PatrickMüllerh, Sieghard Ellenberger i, Dany Azar j,k, Kyoichiro Ueda l, Peter Barna c,ThierryGarciam a Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia b Slovak Academy of Sciences, Institute of Physics, Research Center for Quantum Information, Dúbravská cesta 9, Bratislava 84511, Slovakia c Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, P.O. BOX 106, 840 05 Bratislava, Slovakia d Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya 123, 117868 Moscow, Russia e Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava 84215, Slovakia f Cherepovets State University, Cherepovets 162600, Russia g Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, D-70191 Stuttgart, Germany h Friedhofstraße 9, 66894 Käshofen, Germany i Bodelschwinghstraße 13, 34119 Kassel, Germany j State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, PR China k Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, PO Box 26110217, Fanar - Matn, Lebanon l Kitakyushu Museum, Japan m River Bigal Conservation Project, Avenida Rafael Andrade y clotario Vargas, 220450 Loreto, Orellana, Ecuador article info abstract Article history: Among insects, 236 families in 18 of 44 orders independently invaded water. We report living amphibiotic cock- Received 13 July 2018 roaches from tropical streams of UNESCO BR Sumaco, Ecuador. -
Effects of House and Landscape Characteristics on the Abundance and Diversity of Perimeter Pests Principal Investigators: Arthur G
Project Final Report presented to: The Pest Management Foundation Board of Trustees Project Title: Effects of house and landscape characteristics on the abundance and diversity of perimeter pests Principal Investigators: Arthur G. Appel and Xing Ping Hu, Department of Entomology and Plant Pathology, Auburn University Date: June 17, 2019 Executive Summary: The overall goal of this project was to expand and refine our statistical model that estimates Smokybrown cockroach abundance from house and landscape characteristics to include additional species of cockroaches, several species of ants as well as subterranean termites. The model will correlate pest abundance and diversity with house and landscape characteristics. These results could ultimately be used to better treat and prevent perimeter pest infestations. Since the beginning of the period of performance (August 1, 2017), we have hired two new Master’s students, Patrick Thompson and Gökhan Benk, to assist with the project. Both students will obtain degrees in entomology with a specialization in urban entomology with anticipated graduation dates of summer-fall 2019. We have developed and tested several traps designs for rapidly collecting sweet and protein feeding ants, purchased and modified traps for use during a year of trapping, and have identified species of ants, cockroaches, and termites found around homes in Auburn Alabama. House and landscape characteristics have been measured at 62 single-family homes or independent duplexes. These homes range in age from 7 to 61 years and include the most common different types of siding (brick, metal, stone, vinyl, wood), different numbers/types of yard objects (none to >15, including outbuildings, retaining walls, large ornamental rocks, old trees, compost piles, etc.), and different colors. -
Cockroach Marion Copeland
Cockroach Marion Copeland Animal series Cockroach Animal Series editor: Jonathan Burt Already published Crow Boria Sax Tortoise Peter Young Ant Charlotte Sleigh Forthcoming Wolf Falcon Garry Marvin Helen Macdonald Bear Parrot Robert E. Bieder Paul Carter Horse Whale Sarah Wintle Joseph Roman Spider Rat Leslie Dick Jonathan Burt Dog Hare Susan McHugh Simon Carnell Snake Bee Drake Stutesman Claire Preston Oyster Rebecca Stott Cockroach Marion Copeland reaktion books Published by reaktion books ltd 79 Farringdon Road London ec1m 3ju, uk www.reaktionbooks.co.uk First published 2003 Copyright © Marion Copeland All rights reserved No part of this publication may be reproduced, stored in a retrieval system or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the prior permission of the publishers. Printed and bound in Hong Kong British Library Cataloguing in Publication Data Copeland, Marion Cockroach. – (Animal) 1. Cockroaches 2. Animals and civilization I. Title 595.7’28 isbn 1 86189 192 x Contents Introduction 7 1 A Living Fossil 15 2 What’s in a Name? 44 3 Fellow Traveller 60 4 In the Mind of Man: Myth, Folklore and the Arts 79 5 Tales from the Underside 107 6 Robo-roach 130 7 The Golden Cockroach 148 Timeline 170 Appendix: ‘La Cucaracha’ 172 References 174 Bibliography 186 Associations 189 Websites 190 Acknowledgements 191 Photo Acknowledgements 193 Index 196 Two types of cockroach, from the first major work of American natural history, published in 1747. Introduction The cockroach could not have scuttled along, almost unchanged, for over three hundred million years – some two hundred and ninety-nine million before man evolved – unless it was doing something right. -
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. -
Dictyoptera: Blattaria: Polyphagidae) from Korea Reveal About Cryptocercus Evolution? a Study in Morphology, Molecular Phylogeny, and Chemistry of Tergal Glands
PROCEEDINGS OF THE ACADEMY OF NATURAL SCIENCES OF PHILADELPHIA 151: 61±79. 31 DECEMBER 2001 What does Cryptocercus kyebangensis, n.sp. (Dictyoptera: Blattaria: Polyphagidae) from Korea reveal about Cryptocercus evolution? A study in morphology, molecular phylogeny, and chemistry of tergal glands PHILIPPE GRANDCOLAS,1 YUNG CHUL PARK,2 JAE C. CHOE,3 MARIA-DOLORS PIULACHS,3 XAVIER BELLEÂS,3 CYRILLE D'HAESE,1 JEAN-PIERRE FARINE,4 AND REÂMY BROSSUT4 1ESA 8043 CNRS, Laboratoire d'Entomologie, MuseÂum national d'Histoire naturelle, 45, rue Buffon, 75005 Paris, FranceÐ [email protected] 2School of Biological Sciences, Seoul National University, Kwanak-ku Shilim-dong San 56-1, Seoul 151-742, South Korea 3Department of Physiology and Molecular Biodiversity, Institut de Biologia Molecular de Barcelona (CSIC), Jordi Girona 18, 0834 Barcelona, Spain 4UMR 5548 CNRS, Faculte des Sciences, Universite de Bourgogne, 6, bd. Gabriel, 21000 Dijon, France ABSTRACTÐThe description of a new species of the woodroach Cryptocercus kyebangensis Grandcolas from South Korea offers the opportunity to bring comparative information within the genus. This species, though morphologically very similar to other East Asian and North American species, presents conspicuous differentiation of both ribosomal genes (sequenced fragments of 12S and 16S) and chemical blends from tergal glands (proportions of linalyl acetate and the alcohol 4, 6, 8-trimethyl-7, 9- undecadien-5-ol, compounds previously identi®ed in females originating from North America). A phylogenetic reconstruction involving Blatta orientalis as an outgroup, Therea petiveriana as a polyphagid relative, C. kyebangensis and 17 North American Cryptocercus populations showed that C. kyebangensis stands as a sister-group of North American Cryptocercus, thus suggesting that one beringian vicariance has taken place in the early differentiation of the genus. -
German Cockroach
Pest Profile Photo credit: Gary Alpert, Harvard University, Bugwood.org Common Name: German Cockroach Scientific Name: Blattella germanica Order and Family: Blattodea, Blattellidae Size and Appearance: Length (mm) Appearance Egg Small, brown and purse-shaped containing 30-40 eggs Egg case or ootheca-8mm Larva/Nymph Adult Brown to dark brown coloring with two longitudinal dark 10-15mm bands on the pronotum. Males have their terminal segment of the abdomen visible while the females’ wings cover theirs completely. Pupa (if applicable) Type of feeder (Chewing, sucking, etc.): Chewing mouthparts Host plant/s: German cockroaches are omnivorous, feeding on food scraps, animal feed, paper products, and any kind of garbage. Description of Damage (larvae and adults): German cockroaches are domestic pests that readily infest structures, preferring to inhabit moist areas such as kitchens and bathrooms. They are onsidered to be a public health concern due to their ability to carry pathogens and disperse them. Cockroach feces, shed skins, and body parts are also considered major allergens. In severe instances, biting can occur. German cockroach infestations can readily become a major issue in ideal growth situations. They reproduce continuously and have many overlapping generations that can be present at one time. References: Jacobs, S. (2013). German Cockroaches. Insect Advice from Extension. Pennsylvania State University. https://ento.psu.edu/extension/factsheets/german-cockroaches Valles, S. (2017). German Cockroach-Blattella germanica. Featured Creatures. University of Florida. http://entnemdept.ufl.edu/CREATURES/urban/roaches/german.htm . -
Body-Enlarging Effect of Royal Jelly in a Non-Holometabolous Insect Species, Gryllus Bimaculatus
© 2016. Published by The Company of Biologists Ltd | Biology Open (2016) 5, 770-776 doi:10.1242/bio.019190 RESEARCH ARTICLE Body-enlarging effect of royal jelly in a non-holometabolous insect species, Gryllus bimaculatus Atsushi Miyashita, Hayato Kizaki, Kazuhisa Sekimizu and Chikara Kaito* ABSTRACT (Conlon and Raff, 1999; Otto, 2007). These studies have provided Honeybee royal jelly is reported to have body-enlarging effects in significant insight into the principles of size regulation of living holometabolous insects such as the honeybee, fly and silkmoth, but organisms, although recent concerns over genetically modified its effect in non-holometabolous insect species has not yet been organisms have led researchers to evaluate other types of strategies examined. The present study confirmed the body-enlarging effect in to enlarge animals for industrial purposes. silkmoths fed an artificial diet instead of mulberry leaves used in the As a non-genetic size manipulation, oral ingestion of royal jelly previous literature. Administration of honeybee royal jelly to silkmoth by larvae of the honeybee, Apis mellifera, a holometabolous from early larval stage increased the size of female pupae and hymenopteran insect, induces queen differentiation, leading to adult moths, but not larvae (at the late larval stage) or male pupae. enlarged bodies. Royal jelly contains 12-15% protein, 10-16% We further examined the body-enlarging effect of royal jelly in a sugar, 3-6% lipids (percentages are wet-weight basis), vitamins, non-holometabolous species, the two-spotted cricket Gryllus salts, and free amino acids (Buttstedt et al., 2014). Royal jelly bimaculatus, which belongs to the evolutionarily primitive group contains proteins, named major royal jelly proteins (MRJPs), which Polyneoptera. -
The Control of Turkestan Cockroach Blatta Lateralis (Dictyoptera: Blattidae)
Türk Tarım ve Doğa Bilimleri Dergisi 7(2): 375-380, 2020 https://doi.org/10.30910/turkjans.725807 TÜRK TURKISH TARIM ve DOĞA BİLİMLERİ JOURNAL of AGRICULTURAL DERGİSİ and NATURAL SCIENCES www.dergipark.gov.tr/turkjans Research Article The Control of Turkestan Cockroach Blatta lateralis (Dictyoptera: Blattidae) by The Entomopathogenic nematode Heterorhabditis bacteriophora HBH (Rhabditida: Heterorhabditidae) Using Hydrophilic Fabric Trap Yavuz Selim ŞAHİN, İsmail Alper SUSURLUK* Bursa Uludağ University, Faculty of Agriculture, Department of Plant Protection, 16059, Nilüfer, Bursa, Turkey *Corresponding author: [email protected] Receieved: 09.09.2019 Revised in Received: 18.02.2020 Accepted: 19.02.2020 Abstract Chemical insecticides used against cockroaches, which are an important urban pest and considered public health, are harmful to human health and cause insects to gain resistance. The entomopathogenic nematode (EPN), Heterorhabditis bacteriophora HBH, were used in place of chemical insecticides within the scope of biological control against the Turkestan cockroaches Blatta lateralis in this study. The hydrophilic fabric traps were set to provide the moist environment needed by the EPNs on aboveground. The fabrics inoculated with the nematodes at 50, 100 and 150 IJs/cm2 were used throughout the 37-day experiment. The first treatment was performed by adding 10 adult cockroaches immediately after the establishment of the traps. In the same way, the second treatment was applied after 15 days and the third treatment after 30 days. The mortality rates of cockroaches after 4 and 7 days of exposure to EPNs were determined for all treatments. Although Turkestan cockroaches were exposed to HBH 30 days after the setting of the traps, infection occurred. -
Life Cycle of a Dragonfly, and Will Be Broken Down Into Sections Based on the Chronological Life Stages of This Insect
The Dragonfly Life Cycle Explained A BRIEF DISCUSSION ON THE LIFE CYCLE OF THE COMMON DRAGONFLY Kimberly Malcom | Pennsylvania State University, ENGL 202C: Technical Writing | 2016 Cover Photo: Mitchell, Forrest L and Lasswell, James L., A Dazzle of Dragonflies [Online Image]. Retrieved October 31, 2016 from http://www.audubon.org/magazine/july-august-2012/chasing-dragonflies-and-damselflies Audience and Purpose This document will explain the life cycle of a dragonfly, and will be broken down into sections based on the chronological life stages of this insect. Each section will be further broken down to include a photograph of the stage being discussed, and an explanation of what each stage entails. This document was prepared for the general public, and is meant to be a basic informational description of the life process of the common dragonfly for anyone with a curiosity to learn more about these unique insects. Introduction The dragonfly is a large, colorful, predatory insect generally found in or near watery locations in both the Northern and Southern Hemispheres. There are more than 5,000 known species of dragonflies, and fossil evidence suggests that they’ve been on the earth for many years. They have long, thin, colorful bodies, six legs, large eyes, and two pairs of transparent wings that allow them to propel themselves up, down, forward, backward and side to side Fotolia_1704510_xs [Online Image]. Retrieved October 31, 2016 from http://labs.blogs.com/its_alive_in_the_lab/2009/04/why-dragonfly.html while in flight. They are proficient fliers, and tend to only catch prey and eat while flying. -
Ecological Investigation, Density, Infestation Rate and Control Strategy of German Cockroach, Blattella Germanica (L.) in Two Hospitals in Ismailia, Egypt
Arthropods, 2013, 2(4): 216-224 Article Ecological investigation, density, infestation rate and control strategy of German cockroach, Blattella germanica (L.) in two hospitals in Ismailia, Egypt M.F. Mahmoud, A.F. El-Bahrawy, H.M. El-Sharabasy, Y.S. El-Badry, G.A. El-Kady Plant Protection Department, Faculty of Agriculture, Suez Canal University, 41522 Ismailia, Egypt E-mail: [email protected] Received 2 June 2013; Accepted 8 July 2013; Published online 1 December 2013 Abstract A study was conducted to investigate the ecological situation, density, infestation rate and control strategy of German cockroach, Blattella germanica indoors in two hospitals in Ismailia Governorate, Egypt. The sticky traps method was used for 12 months in 2012. The cockroach index, sanitation and ventilation rate tables were tools to investigate the effectiveness of sanitation and related factors on B. germanica in Ismailia. Results showed that the population density of B. germanica increased gradually from January to July, and then decreased gradually till December of 2012 in both hospitals. The population density of B. germanica captured from hospital 1 (urban) was higher than hospital 2 (rural) in all months. Moreover, the number of German cockroach caught from different apartments in both hospitals was very significant different. Among these apartments, kitchen had the highest number of German cockroach, density, infestation rate and percent of nymphs. The highest population density was in kitchen (298.44), followed by dry food store (69.99), furniture room (25.91) and patient room (8.94), for hospital 1. However, the population was low in all apartments in hospital 2. -
Periodical Cicadas SP 341 3/21 21-0190 Programs in Agriculture and Natural Resources, 4-H Youth Development, Family and Consumer Sciences, and Resource Development
SP 341 Periodical Cicadas Frank A. Hale, Professor Originally developed by Harry Williams, former Professor Emeritus and Jaime Yanes Jr., former Assistant Professor Department of Entomology and Plant Pathology The periodical cicada, Magicicada species, has the broods have been described by scientists and are longest developmental period of any insect in North designated by Roman numerals. There are three 13-year America. There is probably no insect that attracts as cicada broods (XIX, XXII and XXIII) and 12 17-year much attention in eastern North America as does the cicada broods (I-X, XIII, and XIV). Also, there are three periodical cicada. Their sudden springtime emergence, distinct species of 17-year cicadas (M. septendecim, filling the air with their high-pitched, shrill-sounding M. cassini, and M. septendecula) and three species of songs, excites much curiosity. 13-year cicadas (M. tredecim, M. tredecassini, and M. tredecula). Two races of the periodical cicada exist. One race has a life cycle of 13 years and is common in the southeastern In Tennessee, Brood XIX of the 13-year cicada had a United States. The other race has a life cycle of 17 years spectacular emergence in 2011 (Map 1). In 2004 and and is generally more northern in distribution. Due 2021, Brood X of the 17-year cicada primarily emerged to Tennessee’s location, both the 13-year and 17-year in East Tennessee (Map 2). Brood X has the largest cicadas occur in the state. emergence of individuals for the 17-year cicada in the United States. Brood XXIII of the 13-year cicada last Although periodical cicadas have a 13- or 17-year cycle, emerged in West Tennessee in 2015 (Map 3).