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ACTA ENTOMOLOGICA SLOVENICA LJUBLJANA, DECEMBER 2004 Vol
7 Presern 6/2004.xp 24/11/04 11:59 am Page 239 ACTA ENTOMOLOGICA SLOVENICA LJUBLJANA, DECEMBER 2004 Vol. 12, No. 2: 239–248 COMPARISON OF DUNDUBIA VAGINATA (AUCHENORRHYNCHA: CICADOIDEA) SONGS FROM BORNEO AND PENINSULAR MALAYSIA Janez PREØERN1*, Matija GOGALA2, Tomi TRILAR3 1National Institute of Biology, Veœna pot 111, SI - 1000 Ljubljana, Slovenia; e-mail: [email protected] 2Slovenian Academy of Sciences and Arts, Novi trg 3, SI – 1000 Ljubljana, Slovenia; e-mail: [email protected] 3Slovenian Museum of Natural History, Preøernova 20, P.O. Box 290, SI-1001 Ljubljana, Slovenia; e-mail: [email protected] *Corresponding author Abstract - We investigated the songs of the cicada Dundubia vaginata Fabricius 1787. The sound emission analysis is based on 21 recordings of different individuals from four localities in peninsular Malaysia and 10 recordings from one locality in Borneo. The results were compared to the published description of song pattern from Borneo. The song of Dundubia vaginata from peninsular Malaysia is clearly different from Bornean populations’ song. Short, narrow banded frequency modulated (FM) first part of bipartite phrases from Borneo resembles the end short part of phrases from peninsular Malaysia. The longer broadband parts of phrases in both populations have similar properties. A song pattern of unknown sympatric cicada species resembling the song of Bornean population has also been recorded at two localities in peninsular Malaysia. The most prominent difference is unequal length of phrases in the song of this unidentified but probably closely related cicada species. Dundubia vaginata seems to be not a single taxon but rather a complex of species. -
(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. -
Hemiptera: Heteroptera: Pentatomoidea
VIVIANA CAUDURO MATESCO SISTEMÁTICA DE THYREOCORIDAE AMYOT & SERVILLE (HEMIPTERA: HETEROPTERA: PENTATOMOIDEA): REVISÃO DE ALKINDUS DISTANT, MORFOLOGIA DO OVO DE DUAS ESPÉCIES DE GALGUPHA AMYOT & SERVILLE E ANÁLISE CLADÍSTICA DE CORIMELAENA WHITE, COM CONSIDERAÇÕES SOBRE A FILOGENIA DE THYREOCORIDAE, E MORFOLOGIA DO OVO DE 16 ESPÉCIES DE PENTATOMIDAE COMO EXEMPLO DO USO DE CARACTERES DE IMATUROS EM FILOGENIAS Tese apresentada ao Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, como requisito parcial à obtenção do Título de Doutor em Biologia Animal. Área de concentração: Biologia Comparada Orientadora: Profa. Dra. Jocelia Grazia Co-Orientador: Prof. Dr. Cristiano F. Schwertner UNIVERSIDADE FEDERAL DO RIO GRANDE DO SUL PORTO ALEGRE 2014 “Sistemática de Thyreocoridae Amyot & Serville (Hemiptera: Heteroptera: Pentatomoidea): revisão de Alkindus Distant, morfologia do ovo de duas espécies de Galgupha Amyot & Serville e análise cladística de Corimelaena White, com considerações sobre a filogenia de Thyreocoridae, e morfologia do ovo de 16 espécies de Pentatomidae como exemplo de uso de caracteres de imaturos em filogenias” VIVIANA CAUDURO MATESCO Tese apresentada como parte dos requisitos para obtenção de grau de Doutor em Biologia Animal, área de concentração Biologia Comparada. ________________________________________ Prof. Dr. Augusto Ferrari (UFRGS) ________________________________________ Dra. Caroline Greve (CNPq ex-bolsista PDJ) ________________________________________ Prof. Dr. Cláudio José Barros de Carvalho (UFPR) ________________________________________ Profa. Dra. Jocelia Grazia (Orientadora) Porto Alegre, 05 de fevereiro de 2014. AGRADECIMENTOS À minha orientadora, Profa. Dra. Jocelia Grazia, pelos ensinamentos e por todas as oportunidades que me deu durante os treze anos em que estive no Laboratório de Entomologia Sistemática. Ao meu co-orientador, Prof. -
Heteroptera: Cydnidae), with the Description of Two New Species
2021 ACTA ENTOMOLOGICA 61(1): 133–161 MUSEI NATIONALIS PRAGAE doi: 10.37520/aemnp.2021.007 ISSN 1804-6487 (online) – 0374-1036 (print) www.aemnp.eu RESEARCH PAPER Revision of the genus Exosehirus (Heteroptera: Cydnidae), with the description of two new species Dmitry A. GAPON Zoological Institute, Russian Academy of Sciences, 1 Universitetskaya Emb., St Petersburg 199034, Russia; e-mail: [email protected]; ORCID: https://orcid.org/0000-0002-4927-9845 Accepted: Abstract. The present work is a revision of the Palaearctic burrower bug genus Exosehirus th 12 March 2021 Wagner, 1963 (Heteroptera: Cydnidae: Sehirinae). New data on the morphology and distribution Published online: are given. Structures of the female internal ectodermal genitalia and the completely infl ated 21st April 2021 aedeagi are described and illustrated for the fi rst time. An extended diff erential diagnosis as a comparison of the genus with representatives of all Palaearctic genera of the tribe Sehirini is provided. Based on characters of the terminalia of both sexes, two new species are descri- bed: E. elamensis sp. nov. from Southwest Iran, and E. essedonius sp. nov. from Kazakhstan. ‘Exosehirus’ steini (Signoret, 1884) nom. dub. is excluded from the genus Exosehirus and treated as a species incertae sedis. Exosehirus marginatus (Signoret, 1881) is recorded for Azerbaijan for the fi rst time. Key words. Arthroidignatha, Heteroptera, Cydnidae, taxonomy, morphology, male and female terminalia, new species, distribution, Palaearctic Region Zoobank: http://zoobank.org/urn:lsid:zoobank.org:pub:FE96D8BE-6087-436C-8728-7BE849CA13B7 © 2021 The Authors. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Licence. -
Survey on the Singing Cicadas (Auchenorrhyncha: Cicadoidea) of Bulgaria, Including Bioacoustics
ARPHA Conference Abstracts 2: e46487 doi: 10.3897/aca.2.e46487 Conference Abstract Survey on the singing cicadas (Auchenorrhyncha: Cicadoidea) of Bulgaria, including bioacoustics Tomi Trilar‡§, Matija Gogala , Ilia Gjonov| ‡ Slovenian Museum of Natural History, Ljubljana, Slovenia § Slovenian Academy of Sciences and Arts, Ljubljana, Slovenia | Sofia University "St. Kliment Ohridski", Faculty of Biology, Sofia, Bulgaria Corresponding author: Tomi Trilar ([email protected]) Received: 11 Sep 2019 | Published: 11 Sep 2019 Citation: Trilar T, Gogala M, Gjonov I (2019) Survey on the singing cicadas (Auchenorrhyncha: Cicadoidea) of Bulgaria, including bioacoustics. ARPHA Conference Abstracts 2: e46487. https://doi.org/10.3897/aca.2.e46487 Abstract The singing cicadas (Auchenorrhyncha: Cicadoidea) of Bulgaria remain poorly known. There are published records for 14 species (Arabadzhiev 1963, Barjamova 1976, Barjamova 1978, Barjamova 1990, Dirimanov and Harizanov 1965, Dlabola 1955, Gogala et al. 2005, Háva 2016, Janković 1971, Nast 1972, Nast 1987, Nedyalkov 1908, Pelov 1968, Yoakimov 1909): Lyristes plebejus, Cicada orni, Cicadatra atra, C. hyalina, C. persica, Cicadetta montana, C. mediterranea, Oligoglena tibialis, Tympanistalna gastrica, Pagiphora annulata, Dimissalna dimissa, Saticula coriaria, Tibicina haematodes and T. steveni. Two species from this list should be excluded from the list of Bulgarian cicadas, since T. gastrica is distributed in central and southern Portugal (Sueur et al. 2004) and S. coriaria is a north African species (Boulard 1981). We checked three major institutional collections housed in Sofia, Bulgaria: the National Museum of Natural History (NMNHS), Institute of Zoology (ZISB) and Biology Faculty of Sofia University "St. Kliment Ohridski" (BFUS). We confirmed 11 of the species mentioned in the literature, except C. -
Insectts Intestinal Organ for Symbiont Sorting
Insect’s intestinal organ for symbiont sorting PNAS PLUS Tsubasa Ohbayashia, Kazutaka Takeshitaa,b, Wataru Kitagawaa,b, Naruo Nikohc, Ryuichi Kogad, Xian-Ying Mengd, Kanako Tagoe, Tomoyuki Horif, Masahito Hayatsue, Kozo Asanoa, Yoichi Kamagataa,b, Bok Luel Leeg, Takema Fukatsud, and Yoshitomo Kikuchia,b,1 aGraduate School of Agriculture, Hokkaido University, Sapporo 060-8589, Japan; bBioproduction Research Institute, Hokkaido Center, National Institute of Advanced Industrial Science and Technology, Sapporo 062-8517, Japan; cDepartment of Liberal Arts, The Open University of Japan, Chiba 261-8586, Japan; dBioproduction Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8566, Japan; eEnvironmental Biofunction Division, National Institute for Agro-Environmental Sciences, Tsukuba 305-8604, Japan; fEnvironmental Management Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba 305-8569, Japan; and gGlobal Research Laboratory, College of Pharmacy, Pusan National University, Pusan 609-735, Korea Edited by Nancy A. Moran, University of Texas at Austin, Austin, TX, and approved August 11, 2015 (received for review June 11, 2015) Symbiosis has significantly contributed to organismal adaptation Those controlling mechanisms are of general importance for and diversification. For establishment and maintenance of such host– understanding symbiosis (6, 10). symbiont associations, host organisms must have evolved mecha- Stinkbugs, belonging to the insect order Hemiptera, consist of nisms for selective incorporation, accommodation, and maintenance over 40,000 described species in the world (15). The majority of of their specific microbial partners. Here we report the discovery of a the stinkbugs suck plant sap or tissues, and some of them are previously unrecognized type of animal organ for symbiont sorting. -
Burkholderia As Bacterial Symbionts of Lagriinae Beetles
Burkholderia as bacterial symbionts of Lagriinae beetles Symbiont transmission, prevalence and ecological significance in Lagria villosa and Lagria hirta (Coleoptera: Tenebrionidae) Dissertation To Fulfill the Requirements for the Degree of „doctor rerum naturalium“ (Dr. rer. nat.) Submitted to the Council of the Faculty of Biology and Pharmacy of the Friedrich Schiller University Jena by B.Sc. Laura Victoria Flórez born on 19.08.1986 in Bogotá, Colombia Gutachter: 1) Prof. Dr. Martin Kaltenpoth – Johannes-Gutenberg-Universität, Mainz 2) Prof. Dr. Martha S. Hunter – University of Arizona, U.S.A. 3) Prof. Dr. Christian Hertweck – Friedrich-Schiller-Universität, Jena Das Promotionskolloquium wurde abgelegt am: 11.11.2016 “It's life that matters, nothing but life—the process of discovering, the everlasting and perpetual process, not the discovery itself, at all.” Fyodor Dostoyevsky, The Idiot CONTENT List of publications ................................................................................................................ 1 CHAPTER 1: General Introduction ....................................................................................... 2 1.1. The significance of microorganisms in eukaryote biology ....................................................... 2 1.2. The versatile lifestyles of Burkholderia bacteria .................................................................... 4 1.3. Lagriinae beetles and their unexplored symbiosis with bacteria ................................................ 6 1.4. Thesis outline .......................................................................................................... -
Hemiptera: Cicadomorpha: Cicadidae) Found in Poland
POLSKIE PISMO ENTOMOLOGICZNE POLISH JOURNAL OF ENTOMOLOGY VOL. 75: 313–320 Bydgoszcz 30 June 2006 Pyrenean Mountain Cicada Cicadetta cerdaniensis PUISSANT et BOULARD (Hemiptera: Cicadomorpha: Cicadidae) found in Poland TOMI TRILAR*, MATIJA GOGALA**, JACEK SZWEDO*** * Slovenian Museum of Natural History, Prešernova 20, P.O.Box 290, SI-1001 Ljubljana, Slovenia; e-mail: [email protected] ** Slovenian Academy of Sciences and Arts, Novi trg 3, SI-1000 Ljubljana, Slovenia; e-mail: [email protected] *** Department of Systematics and Zoogeography, Museum and Institute of Zoology, Polish Academy of Sciences, Wilcza 64, PL 00-679 Warszawa, Poland; e-mail: [email protected] ABSTRACT. Using recording equipment for sonic and ultrasonic range we recorded and collected Cicadetta cerdaniensis PUISSANT et BOULARD, 2000 on two localities in Poland, at Polana Po- lichno (Nida Valley, Małopolska Upland), and in Ojców National Park (Kraków-Wieluń Upland). These are the first records for the fauna of Poland. Additional new bioacoustic data are included. KEY WORDS: Poland, fauna, new record, singing cicadas, Cicadoidea, Cicadetta cerdaniensis, bioacoustics INTRODUCTION Cicadetta cerdaniensis PUISSANT et BOULARD, 2000 (Hemiptera: Cicadomorpha: Cicadi- dae) is one of the sister species of the Cicadetta montana complex, which has been de- scribed from the Pyrenees (France) on the basis of song pattern (PUISSANT & BOULARD 2000). Sister species of the Cicadetta montana complex, i.e. Cicadetta montana SCOPOLI, 1772, Cicadetta brevipennis (FIEBER, 1876), Cicadetta macedonica (SCHEDL, 1999), Ci- cadetta cerdaniensis PUISSANT et BOULARD, 2000, are morphologically very similar and can be with certainty distinguished only according to species-specific song patterns (GOGALA & TRILAR 2004). Documented are new records of this species on two localities in Poland with additional bioacoustic notes. -
The Food Plants of Some 'Primitive' Pentatomoidea (Hemiptera: Heteroptera)
University of Connecticut OpenCommons@UConn ANSC Articles Department of Animal Science 1988 The food plants of some 'primitive' Pentatomoidea (Hemiptera: Heteroptera). Carl W. Schaefer University of Connecticut, [email protected] Follow this and additional works at: https://opencommons.uconn.edu/ansc_articles Part of the Entomology Commons Recommended Citation Schaefer, Carl W., "The food lp ants of some 'primitive' Pentatomoidea (Hemiptera: Heteroptera)." (1988). ANSC Articles. 9. https://opencommons.uconn.edu/ansc_articles/9 9!E THE FOOD PLANTS OF SOME "PRIWtrTTIVE" PENTATOMOIDEA(HEMIPTERA: HETEROPTERA) CARL W. SCHAEFER Department of Ecotogy and Evolutionar.t Biolog.r, Unit,ersity of Connecticut, Storrs, CT 06268 U.S.A. ,ABSTR.ACT The iood plants of the Cydnidae (Cydninae,Sehirinae, Scaptocorinae, Amnestinae, Garsauriinae, Thau- mastellinae,Parastrachiinae, Corimelaeninae), Plataspidae, Megarididae, Cyrtocoridae, and Lestoniidae, compiled {iom the literature, are discussed.So too are the habitats ofthese insects,most ofwhich live on or are associatedwith the ground. This associationsupports an earlier assertionihat life on the ground was the way of lile o{ the early hemipterans. Most of these groups are polyphagous. However, the Plataspidae feed largely upon legumes, the Scaptocorinaeupon the roots ol Gramineae,some Cydninae also upon legumes,and many Sehirinaeupon members of the advanced dicot subclassAsteridae. Fallen seedsand roots are the preferred plant parts. A group ol mostly small drab shieldbugsappears to be primitive -
Repeated Loss of Variation in Insect Ovary Morphology Highlights the Role of Development in Life-History Evolution
in press at Proceedings of the Royal Society B publication date 05/05/2021 Repeated loss of variation in insect ovary morphology highlights the role of development in life-history evolution Samuel H. Church1*, Bruno A. S. de Medeiros1,2, Seth Donoughe1,3, Nicole L. Márquez Reyes4, Cassandra G. Extavour1,5* 1 Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA 2 Smithsonian Tropical Research Institute, Panama City, Panama 3 Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, IL 60637, USA 4 Department of Biology, Universidad de Puerto Rico en Cayey, Cayey 00736, PR 5 Department of Molecular & Cellular Biology, Harvard University, Cambridge, MA 02138, USA * Corresponding author Abstract The number of offspring an organism can produce is a key component of its evolutionary fitness and life- history. Here we perform a test of the hypothesized trade-off between the number and size of offspring using thousands of descriptions of the number of egg-producing compartments in the insect ovary (ovarioles), a common proxy for potential offspring number in insects. We find evidence of a negative relationship between egg size and ovariole number when accounting for adult body size. However in contrast to prior claims, we note that this relationship is not generalizable across all insect clades, and we highlight several factors that may have contributed to this size-number trade-off being stated as a general rule in previous studies. We reconstruct the evolution of the arrangement of cells that contribute nutrients and patterning information during oogenesis (nurse cells), and show that the diversification of ovariole number and egg size have both been largely independent of their presence or position within the ovariole. -
Hemiptera: Heteroptera) Revealed by Bayesian Phylogenetic Analysis of Nuclear Rdna Sequences 481-496 75 (3): 481– 496 20.12.2017
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Arthropod Systematics and Phylogeny Jahr/Year: 2017 Band/Volume: 75 Autor(en)/Author(s): Lis Jerzy A., Ziaja Dariusz J., Lis Barbara, Gradowska Paulina Artikel/Article: Non-monophyly of the “cydnoid” complex within Pentatomoidea (Hemiptera: Heteroptera) revealed by Bayesian phylogenetic analysis of nuclear rDNA sequences 481-496 75 (3): 481– 496 20.12.2017 © Senckenberg Gesellschaft für Naturforschung, 2017. Non-monophyly of the “cydnoid” complex within Pentatomoidea (Hemiptera: Heteroptera) revealed by Bayesian phylogenetic analysis of nuclear rDNA sequences Jerzy A. Lis *, Dariusz J. Ziaja, Barbara Lis & Paulina Gradowska Department of Biosystematics, Opole University, Oleska 22, 45-052 Opole, Poland; Jerzy A. Lis * [[email protected]]; Dariusz J. Ziaja [[email protected]]; Barbara Lis [[email protected]]; Paulina Gradowska [[email protected]] — * Corresponding author Accepted 02.x.2017. Published online at www.senckenberg.de/arthropod-systematics on 11.xii.2017. Editors in charge: Christiane Weirauch & Klaus-Dieter Klass Abstract The “cydnoid” complex of pentatomoid families, including Cydnidae, Parastrachiidae, Thaumastellidae, and Thyreocoridae, is morphologi- cally defined by the presence of an array of more or less flattened stout setae (called coxal combs), situated on the distal margin of coxae. These structures, suggested to prevent the coxal-trochanteral articulation from injuries caused by particles of soil, sand or dust, by their nature and function are unknown elsewhere in the Heteroptera. As such, coxal combs were regarded as a synapomorphy of this group of families, and enabled the definition of it as a monophylum. -
LEPIDOPTERA: NOCTUIDAE) with ITS HOST PLANT TOMATO Solanum Lycopersicum and the EGG PARASITOID Trichogramma Pretiosum (HYMENOPTERA: TRICHOGRAMMATIDAE
The Pennsylvania State University The Graduate School Department of Entomology OVIPOSITION-MEDIATED INTERACTIONS OF TOMATO FRUITWORM MOTH Helicoverpa zea (LEPIDOPTERA: NOCTUIDAE) WITH ITS HOST PLANT TOMATO Solanum lycopersicum AND THE EGG PARASITOID Trichogramma pretiosum (HYMENOPTERA: TRICHOGRAMMATIDAE) A Dissertation in Entomology by Jinwon Kim © 2013 Jinwon Kim Submitted in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy May 2013 The Dissertation of Jinwon Kim was reviewed and approved* by the following: Gary W. Felton, Ph.D. Professor and Department Head of Entomology Dissertation Advisor Chair of Committee John F. Tooker, Ph.D. Assistant Professor of Entomology James H. Tumlinson, Ph.D. Professor of Entomology Dawn S. Luthe, Ph.D. Professor of Plant Stress Biology *Signatures are on file in the Graduate School i ABSTRACT An increasing number of reports document that, upon deposition of insect eggs, plants induce a variety of defenses to remove the eggs from plant tissue using plant toxic compounds or lending a hand of egg predators and egg parasitoids. In this research, I explored the interactions of tomato fruitworm Helicoverpa zea Boddie (Lepidoptera: Noctuidae) with its host plant tomato Solanum lycopersicum L. (Solanales: Solanaceae) and its egg parasitoid Trichogramma pretiosum (Hymenoptera: Trichogrammatidae) mediated via H. zea eggs laid on tomato plants. In Chapters 2 and 3, tomato’s defensive response to H. zea oviposition was investigated, and in Chapter 4, a novel defense mechanism of H. zea eggs against the egg parasitoid T. pretiosum was explored. The tomato fruitworm moth, H. zea, lays eggs on tomato plants and the larvae emerging from the eggs consume leaves first and then fruit to cause serious loss in the plant fitness.