The Arrival and Spread of the European Firebug Pyrrhocoris
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Mir-2 Family Regulates Insect Metamorphosis by Controlling the Juvenile Hormone Signaling Pathway
MiR-2 family regulates insect metamorphosis by controlling the juvenile hormone signaling pathway Jesus Lozanoa, Raúl Montañeza,b, and Xavier Bellesa,1 aInstitut de Biologia Evolutiva, Consejo Superior de Investigaciones Científicas, Universitat Pompeu Fabra, 08003 Barcelona, Spain; and bInstitució Catalana de Recerca i Estudis Avançats–Complex Systems Laboratory, Universitat Pompeu Fabra, 08003 Barcelona, Spain Edited by Lynn M. Riddiford, Howard Hughes Medical Institute Janelia Farm Research Campus, Ashburn, VA, and approved February 4, 2015 (received for review September 25, 2014) In 2009 we reported that depletion of Dicer-1, the enzyme that we used the cockroach Blattella germanica as a model, because catalyzes the final step of miRNA biosynthesis, prevents meta- it displays the more primitive hemimetabolan mode of meta- morphosis in Blattella germanica. However, the precise regulatory morphosis, where the juvenile stages already have the adult body roles of miRNAs in the process have remained elusive. In the pres- plan, thus making the transition from nymph to adult much less ent work, we have observed that Dicer-1 depletion results in an dramatic than in holometabolan species. In both hemimetabolan increase of mRNA levels of Krüppel homolog 1 (Kr-h1), a juvenile and holometabolan modes the regulation of metamorphosis is ba- hormone-dependent transcription factor that represses metamor- sically ensured by two hormones, the molting hormone (generally phosis, and that depletion of Kr-h1 expression in Dicer-1 knock- 20-hydroxyecdysone), which triggers nonmetamorphic and meta- down individuals rescues metamorphosis. We have also found morphic molts, and the juvenile hormone (JH) that represses the that the 3′UTR of Kr-h1 mRNA contains a functional binding site metamorphic character of the molts (21). -
Climatic Variation of Supercooling Point in the Linden Bug Pyrrhocoris Apterus (Heteroptera: Pyrrhocoridae)
insects Article Climatic Variation of Supercooling Point in the Linden Bug Pyrrhocoris apterus (Heteroptera: Pyrrhocoridae) Tomáš Ditrich 1,* ,Václav Janda 1, Hana Vanˇeˇcková 2 and David Doležel 2 1 Faculty of Education, University of South Bohemia, Branisovska 31a, 37005 Ceske Budejovice, Czech Republic; [email protected] 2 Biology Center, Academy of Sciences of the Czech Republic, 37005 Ceske Budejovice, Czech Republic; [email protected] (H.V.); [email protected] (D.D.) * Correspondence: [email protected]; Tel.: +420-387-773-014 Received: 30 June 2018; Accepted: 15 October 2018; Published: 19 October 2018 Abstract: Cold tolerance is often one of the key components of insect fitness, but the association between climatic conditions and supercooling capacity is poorly understood. We tested 16 lines originating from geographically different populations of the linden bug Pyrrhocoris apterus for their cold tolerance, determined as the supercooling point (SCP). The supercooling point was generally well explained by the climatic conditions of the population’s origin, as the best predictor—winter minimum temperature—explained 85% of the average SCP variation between populations. The supercooling capacity of P. apterus is strongly correlated with climatic conditions, which support the usage of SCP as an appropriate metric of cold tolerance in this species. Keywords: cold tolerance; supercooling point; overwintering; diapause 1. Introduction Population dynamics of temperate insects can be crucially affected by their survival rates during overwintering [1]. Cold tolerance, a key determinant of insect survival during winter, is thus an important research topic for insect ecologists and physiologists. This importance has increased with the recent climate changes around the world, especially in the Northern Hemisphere [2,3]. -
Genetically Modified Baculoviruses for Pest
INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS This page intentionally left blank INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS EDITED BY LAWRENCE I. GILBERT SARJEET S. GILL Amsterdam • Boston • Heidelberg • London • New York • Oxford Paris • San Diego • San Francisco • Singapore • Sydney • Tokyo Academic Press is an imprint of Elsevier Academic Press, 32 Jamestown Road, London, NW1 7BU, UK 30 Corporate Drive, Suite 400, Burlington, MA 01803, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA ª 2010 Elsevier B.V. All rights reserved The chapters first appeared in Comprehensive Molecular Insect Science, edited by Lawrence I. Gilbert, Kostas Iatrou, and Sarjeet S. Gill (Elsevier, B.V. 2005). All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publishers. Permissions may be sought directly from Elsevier’s Rights Department in Oxford, UK: phone (þ44) 1865 843830, fax (þ44) 1865 853333, e-mail [email protected]. Requests may also be completed on-line via the homepage (http://www.elsevier.com/locate/permissions). Library of Congress Cataloging-in-Publication Data Insect control : biological and synthetic agents / editors-in-chief: Lawrence I. Gilbert, Sarjeet S. Gill. – 1st ed. p. cm. Includes bibliographical references and index. ISBN 978-0-12-381449-4 (alk. paper) 1. Insect pests–Control. 2. Insecticides. I. Gilbert, Lawrence I. (Lawrence Irwin), 1929- II. Gill, Sarjeet S. SB931.I42 2010 632’.7–dc22 2010010547 A catalogue record for this book is available from the British Library ISBN 978-0-12-381449-4 Cover Images: (Top Left) Important pest insect targeted by neonicotinoid insecticides: Sweet-potato whitefly, Bemisia tabaci; (Top Right) Control (bottom) and tebufenozide intoxicated by ingestion (top) larvae of the white tussock moth, from Chapter 4; (Bottom) Mode of action of Cry1A toxins, from Addendum A7. -
Pyrrhocoris Apterus (Linnaeus, 1758) - a New Record of Firebug (Hemiptera, Pyrrhocoridae) from Malta
Correspondence BULL. ENT. SOC. MALTA (2019) Vol. 10 : 106–107 DOI: 10.17387/BULLENTSOCMALTA.2019.12 Pyrrhocoris apterus (Linnaeus, 1758) - a new record of firebug (Hemiptera, Pyrrhocoridae) from Malta Thomas CASSAR1 True bugs of the family Pyrrhocoridae, more commonly known as red bugs, cotton stainers or (in the case of Pyrrhocoris apterus) firebugs, are represented by 43 species from 13 genera in the Palaearctic (AUKEMA & RIEGER, 2001). The Heteroptera of the Maltese Islands have been relatively well-studied, with 141 species recorded (CUESTA SEGURA et al., 2010; CARAPEZZA & MIFSUD, 2015; 2016). Of these, only one species belongs to the family Pyrrhocoridae - Scantius aegyptius aegyptius. However, specimens collected in summer of 2018 were confirmed to bePyrrhocoris apterus, a new Pyrrhocorid record for Malta. Pyrrhocoris apterus (Linnaeus, 1758) Material examined: Malta, Ħaż-Żebbuġ, 20.vi.2018, leg. T. Cassar (1 macropterous); Rabat, Chadwick Lakes, 16.ix.2018, leg. T. Cassar (1 brachypterous); Rabat, Chadwick Lakes, 19.ix.2018, leg. T. Cassar (1 brachypterous). Notes: Pyrrhocoris apterus has a predominantly Palaearctic distribution, being present from the Iberian Peninsula eastwards into Siberia and China, including most of central and southern Europe. In controlled conditions, eggs take seven and a half days to hatch (MATOLÍN, 1973). P. apterus goes through five larval instars, the last of which lasts the longest – typically about seven days R( IZKI & SLÁMA, 1968). Adults can be either brachypterous or macropterous, though various intermediate morphs exist. Brachypters’ wings are reduced to vestigial scales whilst macropterous individuals have well-developed pairs of wings which extend to the abdomen tip or past it (SEIDENSTÜCKER, 1953). -
Folk Taxonomy, Nomenclature, Medicinal and Other Uses, Folklore, and Nature Conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3
Ulicsni et al. Journal of Ethnobiology and Ethnomedicine (2016) 12:47 DOI 10.1186/s13002-016-0118-7 RESEARCH Open Access Folk knowledge of invertebrates in Central Europe - folk taxonomy, nomenclature, medicinal and other uses, folklore, and nature conservation Viktor Ulicsni1* , Ingvar Svanberg2 and Zsolt Molnár3 Abstract Background: There is scarce information about European folk knowledge of wild invertebrate fauna. We have documented such folk knowledge in three regions, in Romania, Slovakia and Croatia. We provide a list of folk taxa, and discuss folk biological classification and nomenclature, salient features, uses, related proverbs and sayings, and conservation. Methods: We collected data among Hungarian-speaking people practising small-scale, traditional agriculture. We studied “all” invertebrate species (species groups) potentially occurring in the vicinity of the settlements. We used photos, held semi-structured interviews, and conducted picture sorting. Results: We documented 208 invertebrate folk taxa. Many species were known which have, to our knowledge, no economic significance. 36 % of the species were known to at least half of the informants. Knowledge reliability was high, although informants were sometimes prone to exaggeration. 93 % of folk taxa had their own individual names, and 90 % of the taxa were embedded in the folk taxonomy. Twenty four species were of direct use to humans (4 medicinal, 5 consumed, 11 as bait, 2 as playthings). Completely new was the discovery that the honey stomachs of black-coloured carpenter bees (Xylocopa violacea, X. valga)were consumed. 30 taxa were associated with a proverb or used for weather forecasting, or predicting harvests. Conscious ideas about conserving invertebrates only occurred with a few taxa, but informants would generally refrain from harming firebugs (Pyrrhocoris apterus), field crickets (Gryllus campestris) and most butterflies. -
Climate-Related Transboundary Pests and Diseases
HLC/08/BAK/4 CLIMATE-RELATED TRANSBOUNDARY PESTS AND DISEASES TECHNICAL BACKGROUND DOCUMENT FROM THE EXPERT CONSULTATION HELD ON 25 TO 27 FEBRUARY 2008 FAO, ROME CLIMATE CHANGE AND PEST DISEASES The movement of plant pests, animal diseases and invasive alien aquatic organisms across physical and political boundaries threatens food security and creates a global public concern across all countries and all regions. Countries allocate large resources to limit the spread and control of transboundary pests and diseases 1 such as avian influenza, foot-and-mouth disease and locust. They also adapt animal and plant health services and activities and cooperate regionally and globally for prevention, early warning and control. There is clear evidence that climate change is altering the distribution, incidence and intensity of animal and plant pests and diseases such as Bluetongue, a sheep disease that is moving north into more temperate zones of Europe. Cannon (see Annex 1) found examples of plant pests whose distribution is shifting in the United Kingdom and other parts of Europe, most likely due to climatic factors. For example, migrant moths of the Old World bollworm ( Helicoverpa armigera) had a phenomenal increase in the United Kingdom from 1969-2004 and there have been outbreaks at the northern edge of its range in Europe; cottony cushion scale ( Icerya purchasi) populations appear to be spreading northwards perhaps as a consequence of global warming; and cottony camellia scale ( Pulvinaria – Chloropulvinaria – floccifera) has become much more common in the United Kingdom, extending its range northwards in England and increasing its host range in the last decade or so, which is almost certainly in response to climate change. -
Review of the West Indian Arachnocoris Scott, 1881 (Hemiptera: Nabidae), with Descriptions of Two New Species, and a Catalog of the Species1
Life: The Excitement of Biology 4(1) 32 Review of the West Indian Arachnocoris Scott, 1881 (Hemiptera: Nabidae), with Descriptions of Two New Species, and a Catalog of the Species1 Javier E. Mercado2, Jorge A. Santiago-Blay3, and Michael D. Webb4 Abstract: We review the West Indian species of Arachnocoris, a genus of spider-web dwelling kleptoparasitic nabids. We recognize five species: A. berytoides Uhler from Grenada, A. darlingtoni n. sp. from Hispaniola, A. karukerae Lopez-Moncet from Guadeloupe, A. portoricensis n. sp. from Puerto Rico, and A. trinitatis Bergroth from Trinidad. West Indian Arachnocoris antennal and profemoral color banding patterns are useful diagnostic characters and may have evolved to mimic their spider hosts, which are often island endemic spiders in the family Pholcidae. We provide a simplified and illustrated key to the species based on external characters. A catalog for the 16 recognized species of Arachnocoris is presented. Keywords: Hemiptera, Nabidae, Arachnocoris, new species, Neotropical, West Indies Introduction The Nabidae are a relatively small family in the insect order Hemiptera with approximately 20-30 genera and 400-500 described species (Henry 2009, Faúndez and Carvajal 2014). All described species are terrestrial predators. Some species are considered beneficial to humans as these help control populations of agricultural pests. Several species of Nabis have been reported as biting humans (Faúndez 2015). Within the Nabidae Arachnocoris is one of two genera in the tribe Arachnocorini. The arachnophilic genus5 Arachnocoris Scott is a small and little-known group of specialized kleptoparasitic nabids that spend their life- stages living in a relatively treacherous habitat, namely a spider’s web, particularly non-sticky portions of it (Henry 1999; Mercado-Santiago-Blay 2015; Figure 1, this paper). -
(Kinetoplastea, Trypanosomatidae) in Pyrrhocoris Apterus (Hemiptera, Pyrrhocoridae) Alexander O
Available online at www.sciencedirect.com ScienceDirect European Journal of Protistology 57 (2017) 85–98 Life cycle of Blastocrithidia papi sp. n. (Kinetoplastea, Trypanosomatidae) in Pyrrhocoris apterus (Hemiptera, Pyrrhocoridae) Alexander O. Frolova, Marina N. Malyshevaa, Anna I. Ganyukovaa, Vyacheslav Yurchenkob,c,d, Alexei Y. Kostygova,b,∗ aZoological Institute of the Russian Academy of Sciences, Universitetskaya nab. 1, St. Petersburg 199034, Russia bLife Science Research Centre, Faculty of Science, University of Ostrava, Chittussiho 10, 710 00 Ostrava, Czechia cBiology Centre, Institute of Parasitology, Czech Academy of Sciences, Branisovskᡠ31, 370 05 Ceskéˇ Budejovice (Budweis), Czechia dInstitute of Environmental Technologies, Faculty of Science, University of Ostrava, 710 00 Ostrava, Czechia Received 29 August 2016; received in revised form 7 October 2016; accepted 11 October 2016 Available online 16 November 2016 Abstract Blastocrithidia papi sp. n. is a cyst-forming trypanosomatid parasitizing firebugs (Pyrrhocoris apterus). It is a member of the Blastocrithidia clade and a very close relative of B. largi, to which it is almost identical through its SSU rRNA gene sequence. However, considering the SL RNA gene these two species represent quite distinct, not even related typing units. Morphological analysis of the new species revealed peculiar or even unique features, which may be useful for future taxonomic revision of the genus Blastocrithidia. These include a breach in the microtubular corset of rostrum at the site of contact with the flagellum, absence of desmosomes between flagellum and rostrum, large transparent vacuole near the flagellar pocket, and multiple vacuoles with fibrous content in the posterior portion of the cell. The study of the flagellates’ behavior in the host intestine revealed that they may attach both to microvilli of enterocytes using swollen flagellar tip and to extracellular membranes layers using hemidesmosomes of flagellum. -
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises Michael J. Raupach1*, Lars Hendrich2*, Stefan M. Ku¨ chler3, Fabian Deister1,Je´rome Morinie`re4, Martin M. Gossner5 1 Molecular Taxonomy of Marine Organisms, German Center of Marine Biodiversity (DZMB), Senckenberg am Meer, Wilhelmshaven, Germany, 2 Sektion Insecta varia, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 3 Department of Animal Ecology II, University of Bayreuth, Bayreuth, Germany, 4 Taxonomic coordinator – Barcoding Fauna Bavarica, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 5 Terrestrial Ecology Research Group, Department of Ecology and Ecosystem Management, Technische Universita¨tMu¨nchen, Freising-Weihenstephan, Germany Abstract During the last few years, DNA barcoding has become an efficient method for the identification of species. In the case of insects, most published DNA barcoding studies focus on species of the Ephemeroptera, Trichoptera, Hymenoptera and especially Lepidoptera. In this study we test the efficiency of DNA barcoding for true bugs (Hemiptera: Heteroptera), an ecological and economical highly important as well as morphologically diverse insect taxon. As part of our study we analyzed DNA barcodes for 1742 specimens of 457 species, comprising 39 families of the Heteroptera. We found low nucleotide distances with a minimum pairwise K2P distance ,2.2% within 21 species pairs (39 species). For ten of these species pairs (18 species), minimum pairwise distances were zero. In contrast to this, deep intraspecific sequence divergences with maximum pairwise distances .2.2% were detected for 16 traditionally recognized and valid species. With a successful identification rate of 91.5% (418 species) our study emphasizes the use of DNA barcodes for the identification of true bugs and represents an important step in building-up a comprehensive barcode library for true bugs in Germany and Central Europe as well. -
Commentary Plasticity in Arthropod Cryotypes T
2585 The Journal of Experimental Biology 210, 2585-2592 Published by The Company of Biologists 2007 doi:10.1242/jeb.002618 Commentary Plasticity in arthropod cryotypes T. C. Hawes and J. S. Bale* School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK *Author for correspondence (e-mail: [email protected]) Accepted 12 March 2007 Summary Low-temperature acclimation and acclimatization history and organism is proposed, descending, respectively, produce phenotypic changes in arthropods at multiple from what we define as ‘cryotype’ (class of cryoprotective levels of biological organization from the molecular to the strategy) to genotype and, ultimately, phenotype. behavioural. The role and function of plasticity – where a Alternative (and sometimes complementary) strategies to constitutive, reversible change occurs in the phenotype in plasticity include specialization, generalization, bet- response to low temperature – may be partitioned hedging, cross-resistance and convergence. The transition hierarchically at evolutionary scales according to of cryotypes from basal to derived states is a continuum of cryoprotective strategy, at macrophysiological scales trait optimization, involving the fixation of plasticity and/or according to climatic variability, and at meso- and micro- its alternatives. scales according to ecological niche and exposure. In correspondence with these scales (which are interdependent rather than mutually exclusive), a Key words: arthropod, cold tolerance, cryotype, cryoprotection, hierarchical typology of interaction between thermal acclimation, acclimatization, phenotype. Introduction elasticity depends on the type of rubber band and the stimulus Animal physiology in the real world is dynamic – it must it is given, so the plasticity of an arthropod’s response varies in respond to variability at multiple temporal and spatial scales. -
Native Insects on Non-Native Plants in the Netherlands: Curiosities Or Common Practice?
288 entomologische berichten 72 (6) 2012 Native insects on non-native plants in The Netherlands: curiosities or common practice? Kim Meijer Chris Smit Leo W. Beukeboom Menno Schilthuizen KEY WORDS Herbivorous insects, introduced plants, inventory, phytophagous insects Entomologische Berichten 72 (6): 288-293 In The Netherlands, close to 10% of all plant species occurring in natural habitats are non-native: species that were introduced from e.g. North America or Asia. Insect communities on non-native plants tend to get little attention from many (amateur) entomologists in The Netherlands for two main reasons. First, it is assumed that non-native plant species are not commonly used by herbivorous insects as host plants. Second, many entomologists consider insects associated with non-native plants of minor interest. Here, we give an overview of a large number (99) of native herbivorous insect species collected from non-native plant, clearly showing that non-native plants are used often as host plants. Introduction that species shifting to a novel environment (e.g., ecosystem or Non-native species can cause serious economic damage. In host) suffer less from natural enemies like predators, parasites, North America more than 50,000 species of plants, animals and herbivores and pathogens. Blossey & Nötzold (1995) suggested microbes have been introduced, causing an estimated $137 bil- the ‘Evolution of Increased Competitive Ability Hypothesis’ lion damage annually (Pimentel 2001). Furthermore, in many (EICA) as possible explanation of the success of non-native countries non-native species have a large effect on native spe- species. The EICA predicts that if plants escape from their her- cies and therefore also on the natural ecosystems in which bivores, they will allocate fewer resources to herbivore defence they occur. -
Pyrrhocoris Apterus L. (Hemiptera: Pyrrhocoridae), a Newly Introduced Family, Genus, and Species to Ontario and Canada
Pyrrhocoris apterus , newly introduced to Ontario and Canada JESO Volume 149, 2018 PYRRHOCORIS APTERUS L. (HEMIPTERA: PYRRHOCORIDAE), A NEWLY INTRODUCED FAMILY, GENUS, AND SPECIES TO ONTARIO AND CANADA P. J. OVIEDO RojAS1* AND M. D. JACKsoN1 1University of Guelph: 50 Stone Road East, Guelph, Ontario, Canada N1G 2W1 email, [email protected] Scientific Note J. ent. Soc. Ont. 149: 27–32 The family Pyrrhocoridae (Hemiptera: Pentatomomorpha) has a widespread range, having its greatest diversity in the tropics yet also containing members endemic to the Holarctic region (Schuh and Slater 1995), although none are native to Canada. Dysdercus Guérin-Méneville (Hemiptera: Pyrrhocoridae), which includes the economically important cotton stainers, is the only pyrrhocorid genus with members native to the New World, but is chiefly tropical and more diverse in the Old World (Schaefer 2015). One species has been recorded from as far north as South Carolina and Georgia, USA (Henry 1988a). Pyrrhocoris apterus L. (Hemiptera: Pyrrhocoridae), commonly known as the European firebug, linden bug, or red soldier bug, is found natively throughout Europe and neighbouring regions of Asia. Pyrrhocoris apterus has also been recorded historically from Costa Rica (Distant 1880–1893) and reported in New Jersey, USA in 1896 (Barber 1911; Henry 1988a), though it was not considered established in North America until it was found in Utah, USA in 2008 (Hodgson 2008). This paper will describe the first account of P. apterus, and the family Pyrrhocoridae, in Canada, with evidence that the species has become locally established. The first author first noticed P. apterus in a backyard in Etobicoke, Ontario near the intersection of Martin Grove Road and The Westway (43°41’N 79°34’W) in August 2017.