Plant Galls on Shotover
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Assessment of Forest Pests and Diseases in Protected Areas of Georgia Final Report
Assessment of Forest Pests and Diseases in Protected Areas of Georgia Final report Dr. Iryna Matsiakh Tbilisi 2014 This publication has been produced with the assistance of the European Union. The content, findings, interpretations, and conclusions of this publication are the sole responsibility of the FLEG II (ENPI East) Programme Team (www.enpi-fleg.org) and can in no way be taken to reflect the views of the European Union. The views expressed do not necessarily reflect those of the Implementing Organizations. CONTENTS LIST OF TABLES AND FIGURES ............................................................................................................................. 3 ABBREVIATIONS AND ACRONYMS ...................................................................................................................... 6 EXECUTIVE SUMMARY .............................................................................................................................................. 7 Background information ...................................................................................................................................... 7 Literature review ...................................................................................................................................................... 7 Methodology ................................................................................................................................................................. 8 Results and Discussion .......................................................................................................................................... -
Ants Inhabiting Oak Cynipid Galls in Hungary
North-Western Journal of Zoology 2020, vol.16 (1) - Correspondence: Notes 95 Ants inhabiting oak Cynipid galls in Hungary Oaks are known to harbour extremely rich insect communi- ties, among them more than 100 species of gall wasps (Hy- menoptera: Cynipidae) in Europe (Csóka et al. 2005, Melika 2006). Some gall wasp species are able to induce large and structurally complex galls that can sometimes be abundant on oaks, providing attractive shelters for several arthropod taxa including ant species. Ants are among the most important players in many ecosystems and they are also considered to act as ecosystem engineers (Folgarait, 1998). They are also famous for having ecological or physical interactions with a great variety of other organisms, such as gall wasps. Ants are known to tend Figure 1. Inner structure of the asexual Andricus quercustozae gall in- aphid colonies on the developing galls and, as general pred- habited by ants. ators, they prey on arthropods approaching the protected aphid colonies. Some oak cynipid galls secrete honeydew on their surface. This sweet substrate attracts ants and, in re- turn, the ants protect the galls from predators and parasi- toids (Abe, 1988, 1992; Inouye & Agrawal 2004; Nicholls, 2017). Beyond this obvious ecological interaction between gall wasps and ants, this association continues after the gall wasp’s life cycle has ceased. Certain galls are known to serve as either temporary or permanent shelter for many ant species. Some galls (e.g. An- dricus hungaricus (Hartig), Andricus quercustozae (Bosc), Aphelonyx cerricola (Giraud)) are large enough even for re- productive ant colonies. The advantages of galls as nesting logs are multifaceted. -
National Oak Gall Wasp Survey
ational Oak Gall Wasp Survey – mapping with parabiologists in Finland Bess Hardwick Table of Contents 1. Introduction ................................................................................................................. 2 1.1. Parabiologists in data collecting ............................................................................. 2 1.2. Oak cynipid gall wasps .......................................................................................... 3 1.3. Motivations and objectives .................................................................................... 4 2. Material and methods ................................................................................................ 5 2.1. The volunteers ........................................................................................................ 5 2.2. Sampling ................................................................................................................. 6 2.3. Processing of samples ............................................................................................ 7 2.4. Data selection ........................................................................................................ 7 2.5. Statistical analyses ................................................................................................. 9 3. Results ....................................................................................................................... 10 3.1. Sampling success ................................................................................................. -
The Population Biology of Oak Gall Wasps (Hymenoptera:Cynipidae)
5 Nov 2001 10:11 AR AR147-21.tex AR147-21.SGM ARv2(2001/05/10) P1: GSR Annu. Rev. Entomol. 2002. 47:633–68 Copyright c 2002 by Annual Reviews. All rights reserved THE POPULATION BIOLOGY OF OAK GALL WASPS (HYMENOPTERA:CYNIPIDAE) Graham N. Stone,1 Karsten Schonrogge,¨ 2 Rachel J. Atkinson,3 David Bellido,4 and Juli Pujade-Villar4 1Institute of Cell, Animal, and Population Biology, University of Edinburgh, The King’s Buildings, West Mains Road, Edinburgh EH9 3JT, United Kingdom; e-mail: [email protected] 2Center of Ecology and Hydrology, CEH Dorset, Winfrith Technology Center, Winfrith Newburgh, Dorchester, Dorset DT2 8ZD, United Kingdom; e-mail: [email protected] 3Center for Conservation Science, Department of Biology, University of Stirling, Stirling FK9 4LA, United Kingdom; e-mail: [email protected] 4Departamento de Biologia Animal, Facultat de Biologia, Universitat de Barcelona, Avenida Diagonal 645, 08028 Barcelona, Spain; e-mail: [email protected] Key Words cyclical parthenogenesis, host alternation, food web, parasitoid, population dynamics ■ Abstract Oak gall wasps (Hymenoptera: Cynipidae, Cynipini) are characterized by possession of complex cyclically parthenogenetic life cycles and the ability to induce a wide diversity of highly complex species- and generation-specific galls on oaks and other Fagaceae. The galls support species-rich, closed communities of inquilines and parasitoids that have become a model system in community ecology. We review recent advances in the ecology of oak cynipids, with particular emphasis on life cycle characteristics and the dynamics of the interactions between host plants, gall wasps, and natural enemies. We assess the importance of gall traits in structuring oak cynipid communities and summarize the evidence for bottom-up and top-down effects across trophic levels. -
Contents Hawthorn Dene, 1, 5-Jul-1924
Northern Naturalists’ Union Field Meeting Reports- 1924-2005 Contents Hawthorn Dene, 1, 5-jul-1924 .............................. 10 Billingham Marsh, 2, 13-jun-1925 ......................... 13 Sweethope Lough, 3, 11-jul-1925 ........................ 18 The Sneap, 4, 12-jun-1926 ................................... 24 Great Ayton, 5, 18-jun-1927 ................................. 28 Gibside, 6, 23-jul-1927 ......................................... 28 Langdon Beck, 7, 9-jun-1928 ............................... 29 Hawthorn Dene, 8, 5-jul-1928 .............................. 33 Frosterley, 9 ......................................................... 38 The Sneap, 10, 1-jun-1929 ................................... 38 Allenheads, 11, 6-july-1929 .................................. 43 Dryderdale, 12, 14-jun-1930 ................................. 46 Blanchland, 13, 12-jul-1930 .................................. 49 Devil's Water, 14, 15-jun-1931 ............................. 52 Egglestone, 15, 11-jul-1931 ................................. 53 Windlestone Park, 16, June? ............................... 55 Edmondbyers, 17, 16-jul-1932 ............................. 57 Stanhope and Frosterley, 18, 5-jun-1932 ............. 58 The Sneap, 19, 15-jul-1933 .................................. 61 Pigdon Banks, 20, 1-jun-1934 .............................. 62 Greatham Marsh, 21, 21-jul-1934 ........................ 64 Blanchland, 22, 15-jun-1935 ................................ 66 Dryderdale, 23, ..................................................... 68 Raby Park, -
Community Level Consequences of Adaptive Management Through Climate Matching: Oak Galls As a Model System
Community level consequences of adaptive management through Climate Matching: oak galls as a model system Frazer H. Sinclair Submitted for the degree of Doctor of Philosophy University of Edinburgh 2011 1 Declaration This thesis is submitted to the University of Edinburgh in accordance with the requirements for the degree of Doctor of Philosophy in the College of Science and Engineering. Aspects of the presented work were made possible by collaboration and data sharing with individuals and institutions, details of which are presented below. Chapter 2. The French National Institute for Agricultural Research (INRA) provided various phenotypic and genotypic data from oak provenance trials that are under their management. All presented analyses of these data are my own. Chapter 3. INRA allowed access to their established oak provenance trial at the forest of Petite Charnie in Sarthe, Northwest France. Insect surveys at the trial were conducted by me, and by volunteers under my supervision. All presented analyses of these data are my own. Chapter 4. Insect specimens were collected by me from the oak provenance trial at Petite Charnie with the permission of INRA. Approximately 1/3 of DNA extractions and PCR reactions were conducted by Konrad Lohse, Julja Ernst, and Juan Carlos Ruiz Guajardo. All presented analyses are my own. Chapter 5. Insect specimens were sourced from the Stone laboratory collections at the University of Edinburgh. Unpublished DNA sequence data from 6 parasitoid individuals were provided by Konrad Lohse. All presented analysis of this data is my own. Unless otherwise stated, the remaining work and content of this thesis are entirely my own. -
Torymus Sinensis Against the Chestnut Gall Wasp Dryocosmus Kuriphilus in the Canton Ticino, Switzerland
| January 2011 Evaluating the use of Torymus sinensis against the chestnut gall wasp Dryocosmus kuriphilus in the Canton Ticino, Switzerland Authors Aebi Alexandre, Agroscope ART Schoenenberger Nicola, Tulum SA and Bigler Franz, Agroscope ART Torymus sinensis against the chestnut gall wasp Dryocosmus kuriphilus | January 2011 1 Zürich/Caslano, January 2011 Authors’ affiliation: Alexandre Aebi and Franz Bigler Nicola Schoenenberger Agroscope Reckenholz-Tänikon TULUM SA Research Station ART Via Rompada 40 Biosafety 6987 Caslano Reckenholzstrasse 191 Switzerland 8046 Zürich Tel: +41 91 606 6373 Switzerland Fax: +41 44 606 6376 Tel: +41 44 377 7669 [email protected] Fax: +41 44 377 7201 [email protected] This work was financed by the Swiss Federal Office for the Environment (FOEN) This work was done in collaboration with B. Bellosi and E. Schaltegger (TULUM SA) Cover figure: Empty chestnut gall in Stabio, February 2010 (Picture:TULUM SA) All maps used in figures and appendices (except Fig. 6): ©swisstopo, license number: DV053809.1 Map in figure 6: © Istituto Geografico, De Agostini 1982–1988 ISBN 978-3-905733-20-4 © 2010 ART 2 Torymus sinensis against the chestnut gall wasp Dryocosmus kuriphilus | January 2011 Table of contents Table of contents Abstract 5 1. Introduction 6 2. Mission and methods 7 3. Presence and degree of infestation of Dryocosmus kuriphilus in Switzerland 9 4. Invasion corridors of Dryocosmus kuriphilus towards Switzerland 11 5. Potential economic and ecological damage caused by Dryocosmus kuriphilus in Switzerland 14 6. Release of the parasitoid Torymus sinensis in the Piedmont Region, Italy 17 7. Potential benefits and damage due to the release of Torymus sinensis 18 8. -
Impacts of Local Adaptation of Forest Trees on Associations with Herbivorous Insects: Implications for Adaptive Forest Management
Edinburgh Research Explorer Impacts of local adaptation of forest trees on associations with herbivorous insects: implications for adaptive forest management Citation for published version: Sinclair, FH, Stone, GN, Nicholls, JA, Cavers, S, Gibbs, M, Butterill, P, Wagner, S, Ducousso, A, Gerber, S, Petit, RJ, Kremer, A & Sch??nrogge, K 2015, 'Impacts of local adaptation of forest trees on associations with herbivorous insects: implications for adaptive forest management', Evolutionary Applications, vol. 8, no. 10, pp. 972–987. https://doi.org/10.1111/eva.12329 Digital Object Identifier (DOI): 10.1111/eva.12329 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: Evolutionary Applications Publisher Rights Statement: © 2015 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and eproduction in any medium, provided the original work is properly cited. General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact [email protected] providing details, and we will remove access to the work immediately and investigate your claim. -
Parasitoids, Hyperparasitoids, and Inquilines Associated with the Sexual and Asexual Generations of the Gall Former, Belonocnema Treatae (Hymenoptera: Cynipidae)
Annals of the Entomological Society of America, 109(1), 2016, 49–63 doi: 10.1093/aesa/sav112 Advance Access Publication Date: 9 November 2015 Conservation Biology and Biodiversity Research article Parasitoids, Hyperparasitoids, and Inquilines Associated With the Sexual and Asexual Generations of the Gall Former, Belonocnema treatae (Hymenoptera: Cynipidae) Andrew A. Forbes,1,2 M. Carmen Hall,3,4 JoAnne Lund,3,5 Glen R. Hood,3,6 Rebecca Izen,7 Scott P. Egan,7 and James R. Ott3 Downloaded from 1Department of Biology, University of Iowa, Iowa City, IA 52242 ([email protected]), 2Corresponding author, e-mail: [email protected], 3Population and Conservation Biology Program, Department of Biology, Texas State University, San Marcos, TX 78666 ([email protected]; [email protected]; [email protected]; [email protected]), 4Current address: Science Department, Georgia Perimeter College, Decatur, GA 30034, 5Current address: 4223 Bear Track Lane, Harshaw, WI 54529, 6Current address: Department of Biological Sciences, University of Notre Dame, Galvin Life Sciences, Notre Dame, IN 46556, and 7Department of BioSciences, Anderson Biological Laboratories, Rice University, Houston, TX 77005 ([email protected], http://aesa.oxfordjournals.org/ [email protected]) Received 24 July 2015; Accepted 25 October 2015 Abstract Insect-induced plant galls are thought to provide gall-forming insects protection from predation and parasitism, yet many gall formers experience high levels of mortality inflicted by a species-rich community of insect natural enemies. Many gall-forming cynipid wasp species also display heterogony, wherein sexual (gamic) and asexual at Univ. of Massachusetts/Amherst Library on March 14, 2016 (agamic) generations may form galls on different plant tissues or plant species. -
The Entomologist's Record and Journal of Variation
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Interaktionen Zwischen Wirten Und Parasitoiden
Interaktionen zwischen Wirten und Parasitoiden: Nahrungsnetzstruktur, Wirtsspektren und Wirtsfindung am Beispiel der Arten aus Vogelnestern (Insecta: Diptera: Cyclorrhapha und Hymenoptera: Chalcidoidea) Dissertation zur Erlangung des Doktorgrades des Departments Biologie der Fakultät für Mathematik, Informatik und Naturwissenschaften an der Universität Hamburg vorgelegt von Ralph Peters aus Hamburg Dezember 2006 Inhalt Interaktionen zwischen Wirten und Parasitoiden: Nahrungsnetzstruktur, Wirtsspektren und Wirtsfindung am Beispiel der Arten aus Vogelnestern (Insecta: Diptera: Cyclorrhapha und Hymenoptera: Chalcidoidea) Inhalt: 1. Einleitung .......................................................................................................................... 1 2. Material und Methoden .................................................................................................... 4 2.1 Datenerhebung für das Nahrungsnetz / „parasitoid web“ ...................................... 4 2.1.1 Materialsammlung und -weiterbehandlung .................................................................... 4 2.1.2 Weitere Datenerhebung für das „parasitoid web“ ................................................................. 5 2.2 Material und Methoden der Untersuchungen zur Parasitoidenbiologie ................ 6 2.2.1 Morphologische Untersuchungen in der Gattung Dibrachys ................................................ 6 2.2.2 Labornachzuchten zur Erstellung der Wirtsspektren .......................................................... 10 2.2.3 -
Zoologische Mededelingen
ZOOLOGISCHE MEDEDELINGEN UITGEGEVEN DOOR HET RIJKSMUSEUM VAN NATUURLIJKE HISTORIE TE LEIDEN (MINISTERIE VAN CULTUUR, RECREATIE EN MAATSCHAPPELIJK WERK) Deel 53 no. 28 29 juni 1979 A CHARACTER ANALYSIS OF THE SPECIES OF SYNERGUS HARTIG, SECTION II (MAYR, 1872) (HYMENOPTERA, CYNIPIDAE) by A. A. WIEBES - RIJKS Afdeling Systematische Dierkunde der Rijksuniversiteit, Leiden With 83 text-figures ABSTRACT A survey is given of the characters used for the differentiation of the species of Synergus Hartig, classified with section II of Mayr. Special attention is given to the phenology of the species, for each of which the life-cycle is schematized, with differentia- tion in spring- and summer-generation. Two forms, provisionally indicated A and B, could not satisfactorily be identified with any of the known species. Sp. В is a common inquiline of oak-apples; biological observations were made on the larvae. Synergus mutabilis Deitmer, 1924, is synonymized with Synergus albipes Hartig, 1841. The identification of the species of Synergus Hartig, 1840, is notoriously difficult, particularly of those classified in section II (Mayr, 1872). The species of section I, single brooded, that winter in galls as late-stage larvae or pupae and emerge in early summer, are easier to be identified (Eady, 1952). Some of the difficulties with section II may stem from the fact that many species produce two broods in one year, often dissimilar in appearance (Ross, 1951). It should be stated that in all instances the correlations of spring and summer generations were deduced from circumstantial evidence: no specimens were actually reared from one generation to another. Even more confusing than the alternation of broods may be the great variation pre sumably caused by differences in quantity or quality of larval food.