Thysanoptera, Aeolothripidae) from Iran
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Haplothrips Leucanthemi Distinguishing Features Both Sexes Fully Winged
Haplothrips leucanthemi Distinguishing features Both sexes fully winged. Body brown to dark brown, fore tarsi and base of antennal segment III yellow; fore wing pale with base extensively shaded. Head slightly longer than wide; maxillary stylets one third of head width apart, retracted to postocular setae, maxillary bridge complete; postocular setae short and acute, usually not reaching posterior margin of compound eyes. Antennae 8-segmented, segment III with 2 sense cones, IV with 4 sense cones; VIII short and broad at base. Pronotal setae small and acute, anteromarginal and midlateral setae no longer than discal setae; prosternal basantra and ferna present, mesopresternum eroded to paired lateral triangles. Fore tarsal tooth minute in female. Fore wing constricted medially, with 7–12 duplicated cilia, sub-basal setae acute or blunt. Tergite Antenna IX setae S1 bluntly pointed, much shorter than tube, S2 acute. Male with large fore tarsal tooth; tergite IX setae S2 short and stout; pseudovirga of aedeagus slender. Related species The genus Haplothrips comprises 240 described species worldwide, of which only four are recorded from New Zealand, and none of these seems to be endemic. H. leucanthemi is a European species that is particularly associated with the flowers of Chrysanthemum leucanthemum. A form of this species is associated with red clover flowers and has been known as H. niger, but this is considered to be a parthenogenetic strain of H. leucanthemi. This thrips is remarkable among Haplothrips species in Head & pronotum having unusually short setae on the head and pronotum. Biological data Breeding and pupating within flowers, particularly Chrysanthemum leucanthemum (Asteraceae), but also Trifolium sp. -
Departament De Biologia Funcional I Antropologia Física
DEPARTAMENT DE BIOLOGIA FUNCIONAL I ANTROPOLOGIA FÍSICA EVALUACIÓN DE MECANISMOS DE RESISTENCIA A INSECTICIDAS EN FRANKLINIELLA OCCIDENTALIS (PERGANDE): IMPLICACIÓN DE CARBOXILESTERASAS Y ACETILCOLINESTERASAS NEUS LÓPEZ SOLER UNIVERSITAT DE VALÈNCIA Servei de Publicacions 2008 Aquesta Tesi Doctoral va ser presentada a València el dia 26 de juny de 2008 davant un tribunal format per: - D. Rafael Martínez Pardo - D. Félix Ortego Alonso - D. Juan Ferré Manzanero - D. Francisco José Beitia Crespo - D. Juan Javier Díaz Mayans Va ser dirigida per: Dª. Mª Dolores Garcerá Zamorano Dª. Amelia Cervera Olagüe ©Copyright: Servei de Publicacions Neus López Soler Depòsit legal: I.S.B.N.: 978-84-370-7227-2 Edita: Universitat de València Servei de Publicacions C/ Artes Gráficas, 13 bajo 46010 València Spain Telèfon: 963864115 Facultat de Ciències Biològiques Departament de Biologia Funcional i Antropologia Física Evaluación de mecanismos de resistencia a insecticidas en Frankliniella occidentalis (Pergande): implicación de carboxilesterasas y acetilcolinesterasas Neus López Soler Burjassot, València 2008 i Tesis presentada por Neus López Soler para optar al grado de Doctor en Ciencias Biológicas por la Universitat de València. Fdo. Neus López Soler Tesis dirigida por: Mª Dolores Garcerá Zamorano, Doctora en Ciencias Biológicas y Catedrática de Fisiología de la Universitat de València. Amelia Cervera Olagüe, Doctora en Ciencias Biológicas. Fdo. Mª Dolores Garcerá Zamorano Fdo. Amelia Cervera Olagüe La investigación presentada en esta Tesis se realizó en la Unidad de Fisiología Animal del Departament de Biologia Funcional i Antropologia Física de la Facultat de Ciències Biològiques de la Universitat de València, gracias al disfrute de una Beca del Programa Nacional de Formación de Profesorado Universitario (FPU) del Ministerio de Educación y Ciencia. -
Thysanoptera: Aeolothripidae)
Zootaxa 4683 (3): 447–450 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Correspondence ZOOTAXA Copyright © 2019 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4683.3.9 http://zoobank.org/urn:lsid:zoobank.org:pub:3CA08D86-8574-446F-8FC9-7B6BADBDBCA3 Reduced antennal segmentation in a new species from Iran of the genus Aeolothrips (Thysanoptera: Aeolothripidae) KAMBIZ MINAEI1 & LAURENCE MOUND2 1Department of Plant Protection, College of Agriculture, Shiraz University, Shiraz, Iran. E-mail: [email protected] 2CSIRO Australian national Insect Collection, Canberra, ACT, Australia. E-mail: [email protected] The number of antennal segments in adults of the different families and genera in the insect order Thysanoptera varies between five and nine. The plesiotypic number is considered to be nine (Zhang et al. 2019), and fossil thrips reported to have 10 to 15 segments (Tong et al. 2019) are generally considered to be aberrations in which the terminal segment bears transverse striae. The 9-segmented condition occurs particularly amongst species that exhibit several other characters in a plesiomorphic state, including all Melanthripidae, two genera of Merothripidae, also most species of Fauriellidae, Stenu- rothripidae, Heterothripidae, and Aeolothripidae (Mound et al. 1980). Curiously, members of a few genera of Thripidae (Palmer & Mound 1985; Minaei 2012) also have nine antennal segments, but this is considered a reversion from the 8- segmented condition that is assumed to be plesiomorphic for that family (Zhang et al. 2019). Variation between eight and nine segments occurs in the genus Anaphothrips, and within that genus a few species exhibit intraspecific variation in an- tennal segmentation (Mound & Masumoto 2009). -
Heterothripidae Australian Fauna No Member of This Family Is Known from Australia
Index | Glossary A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Heterothripidae Australian fauna No member of this Family is known from Australia. Biology Of the 90 species currently listed in this family, all but the five Aulacothrips species are considered to be phytophagous. They feed and breed in flowers, presumably exhibiting a high Heterothrips arisaemae, female Heterothrips arisaemae, antenna level of host specificity (Mound & Marullo, 1996), and pupate in a silken cocoon at soil level. Aulacothrips species breed on, and pupate on, the tergites of particular Homoptera, feeding as ectoparasites on these bugs (Izzo et al., 2002; Cavalleri & Kaminski, 2014). Geographic distribution Heterothrips arisaemae, antennal Aulacothrips dictyotus, antennal segments III-IV segments IV-IX Members of this family are known only from the Americas, and keys to many species are provided by Mound & Marullo (1996), and Pereyra & Cavalleri (2012). Species of Heterothrips have been described between New York and Illinois in the North and Argentina in the South, whereas the species of the other three genera are known only from the Neotropics. Heterothrips arisaemae, wings Recognition Heterothrips arisaemae, head & pronotum Species of Heterothripidae all have nine antennal segments, the distal segments being more or less distinct from each other, and the sensoria on segments III and IV form a continuous band. In most species this sensorium is only around the segment apex, but in Lenkothrips it extends as a loop to the midpoint of both segments, and in Aulacothrips it is looped and highly convoluted Heterothrips arisaemae, Heterothrips arisaemae, tergites I- (Cavalleri & Kaminski, 2014). -
Haplothrips Aliakbarii Sp. Nov. (Thysanoptera: Phlaeothripidae): a New Thrips on Oak Trees from Ilam Province (Western Iran)
Turkish Journal of Zoology Turk J Zool (2018) 42: 608-613 http://journals.tubitak.gov.tr/zoology/ © TÜBİTAK Short Communication doi:10.3906/zoo-1805-27 Haplothrips aliakbarii sp. nov. (Thysanoptera: Phlaeothripidae): a new thrips on oak trees from Ilam Province (western Iran) Majid MIRAB-BALOU*, Behzad MIRI Department of Plant Protection, College of Agriculture, Ilam University, Ilam, Iran Received: 18.05.2018 Accepted/Published Online: 12.08.2018 Final Version: 17.09.2018 Abstract: Haplothrips aliakbarii sp. nov. (Phlaeothripidae: Phlaeothripinae) is described and illustrated from Ilam Province, western Iran. This new species was collected on the leaves of oak trees (Quercus brantii). An identification key for Iranian species of Haplothrips is presented. Key words: Haplothrips, new species, oak, key, Iran Species of the large genus Haplothrips Amyot & Serville Bagnall, H. kurdjumovi Karny, H. longipes Bagnall, H. (Phlaeothripinae: Haplothripini) are found worldwide, maroccanus Priesner, H. minutes Uzel, H. phyllophilus with 242 extant species (Mound and Matsunaga, 2017). Priesner, H. rabinovitchi Priesner, and H. subtilissimus This genus is divided into two subgenera, Haplothrips and (Haliday). Trybomiella, which are distinguished by the presence or In this paper, we describe a new species of Haplothrips absence of fore wings with duplicated cilia (Minaei and that was collected on the leaves of oak trees in Ilam Mound, 2008). Species of this genus are usually brown and Province, western Iran. An identification key is also are readily recognized from the head gradually narrowed provided for 21 species of Haplothrips from Iran (Minaei towards base, postocular setae pointed, blunt or expanded; and Mound, 2008), and an updated key is provided for antennae 8-segmented, segment III with one or two sense Iranian species of this genus. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Western Flower Thrips (Frankliniella Occidentalis [Pergande])1 Jeffrey D
ENY-883 Western Flower Thrips (Frankliniella occidentalis [Pergande])1 Jeffrey D. Cluever, Hugh A. Smith, Joseph E. Funderburk, and Galen Frantz2 Introduction Taxonomy Many species of thrips can be found in Florida. These The order Thysanoptera consists of more than 5,000 species include adventive species like Frankliniella occidentalis, in two suborders, Tubulifera and Terebrantia. The suborder Frankliniella schultzei, Thrips palmi, and Scirtothrips Tubulifera has over 3,000 species in one family, Phlaeo- dorsalis. Native species include Frankliniella tritici and thripidae. The suborder Terebrantia consists of over 2,000 Frankliniella bispinosa. Frankliniella occidentalis is a pest species in seven families. Thripidae is the largest of these of several crops throughout Florida and the world and is families, with about 1,700 species. It includes genera such capable of causing economic loss (Fig. 1). as Scirtothrips, Thrips, and Frankliniella (Mound and Teulon 1995; Mound et al. 2009). Synonyms The original name for Frankliniella occidentalis was Euthrips occidentalis Pergande 1895 (Hoddle et al. 2012; GBIF 2014). This species has a high number of synonymies as a result of the variability that Frankliniella occidentalis has in structure and color in its native range. Some other synonyms are (CABI 2014): Euthrips helianthi Moulton 1911 Euthrips tritici var. californicus Moulton 1911 Figure 1. Western flower thrips adult. Frankliniella californica Moulton Credits: Lyle Buss Frankliniella tritici var. moultoni Hood 1914 1. This document is ENY-883, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date April 2015. Reviewed June 2018. Visit the EDIS website at http://edis.ifas.ufl.edu. -
Thysanoptera)
A peer-reviewed open-access journal ZooKeys 786: 59–68 (2018)One generic synonym and one new species of Phlaeothripidae... 59 doi: 10.3897/zookeys.786.28332 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research One generic synonym and one new species of Phlaeothripidae from India (Thysanoptera) Kaomud Tyagi1, Devkant Singha1,2, Goutam Kumar Saha2, Vikas Kumar1 1 Centre for DNA Taxonomy (CDT), Molecular Systematics Division, Zoological Survey of India, Kolkata, West Bengal, India 2 Department of Zoology, University of Calcutta, West Bengal, India Corresponding author: Kaomud Tyagi ([email protected]) Academic editor: Laurence Mound | Received 12 July 2018 | Accepted 3 August 2018 | Published 25 September 2018 http://zoobank.org/BFDE9229-D4F5-4FCF-B9FD-59AF8C1FA826 Citation: Tyagi K, Singha D, Saha GK, Kumar V (2018) One generic synonym and one new species of Phlaeothripidae from India (Thysanoptera). ZooKeys 786: 59–68.https://doi.org/10.3897/zookeys.786.28332 Abstract Haplothrips shivendraii Tyagi & Kumar, sp. n. is described from Rajasthan state of India. The monobasic Austro-oriental genus Dyothrips Kudô is formally synonymised with Haplothrips. Keywords Dyothrips, Haplothrips, India, new species, synonym. Introduction The generaHaplothrips , Dyothrips, and Plicothrips belong to tribe Haplothripini in the subfamily Phlaeothripinae, family Phlaeothripidae (Mound and Minaei 2007, Minaei and Mound 2008). Haplothrips was erected by Amyot and Serville (1843) for the single species, Phloeothrips albipennis Burmeister, 1836. It is the second largest genus in the family Phlaeothripidae and comprises the two subgenera Haplothrips and Trybomiella. These are distinguished by the presence or absence of fore wing duplicated cilia, pre- sent in Haplothrips and absent in Trybomiella. -
First Insight Into Microbiome Profile of Fungivorous Thrips Hoplothrips Carpathicus (Insecta: Thysanoptera) at Different Develop
www.nature.com/scientificreports OPEN First insight into microbiome profle of fungivorous thrips Hoplothrips carpathicus (Insecta: Thysanoptera) Received: 19 January 2018 Accepted: 12 September 2018 at diferent developmental stages: Published: xx xx xxxx molecular evidence of Wolbachia endosymbiosis Agnieszka Kaczmarczyk 1, Halina Kucharczyk2, Marek Kucharczyk3, Przemysław Kapusta4, Jerzy Sell1 & Sylwia Zielińska5,6 Insects’ exoskeleton, gut, hemocoel, and cells are colonized by various microorganisms that often play important roles in their host life. Moreover, insects are frequently infected by vertically transmitted symbionts that can manipulate their reproduction. The aims of this study were the characterization of bacterial communities of four developmental stages of the fungivorous species Hoplothrips carpathicus (Thysanoptera: Phlaeothripidae), verifcation of the presence of Wolbachia, in silico prediction of metabolic potentials of the microorganisms, and sequencing its mitochondrial COI barcode. Taxonomy- based analysis indicated that the bacterial community of H. carpathicus contained 21 bacterial phyla. The most abundant phyla were Proteobacteria, Actinobacteria, Bacterioidetes and Firmicutes, and the most abundant classes were Alphaproteobacteria, Actinobacteria, Gammaproteobacteria and Betaproteobacteria, with diferent proportions in the total share. For pupa and imago (adult) the most abundant genus was Wolbachia, which comprised 69.95% and 56.11% of total bacterial population respectively. Moreover, similarity analysis of bacterial communities showed that changes in microbiome composition are congruent with the successive stages of H. carpathicus development. PICRUSt analysis predicted that each bacterial community should be rich in genes involved in membrane transport, amino acid metabolism, carbohydrate metabolism, replication and repair processes. Insects are by far the most diverse and abundant animal group, in numbers of species globally, in ecological habits, and in biomass1. -
ON Frankliniella Occidentalis (Pergande) and Frankliniella Bispinosa (Morgan) in SWEET PEPPER
DIFFERENTIAL PREDATION BY Orius insidiosus (Say) ON Frankliniella occidentalis (Pergande) AND Frankliniella bispinosa (Morgan) IN SWEET PEPPER By SCOT MICHAEL WARING A THESIS PRESENTED TO THE GRADUATE SCHOOL OF THE UNIVERSITY OF FLORIDA IN PARTIAL FULFILLMENT OF THE REQUIREMENT FOR THE DEGREE OF MASTER OF SCIENCE UNIVERSITY OF FLORIDA 2005 ACKNOWLEDGMENTS I thank my Mom for getting me interested in what nature has to offer: birds, rats, snakes, bugs and fishing; she influenced me far more than anyone else to get me where I am today. I thank my Dad for his relentless support and concern. I thank my son, Sequoya, for his constant inspiration and patience uncommon for a boy his age. I thank my wife, Anna, for her endless supply of energy and love. I thank my grandmother, Mimi, for all of her love, support and encouragement. I thank Joe Funderburk and Stuart Reitz for continuing to support and encourage me in my most difficult times. I thank Debbie Hall for guiding me and watching over me during my effort to bring this thesis to life. I thank Heather McAuslane for her generous lab support, use of her greenhouse and superior editing abilities. I thank Shane Hill for sharing his love of entomology and for being such a good friend. I thank Tim Forrest for introducing me to entomology. I thank Jim Nation and Grover Smart for their help navigating graduate school and the academics therein. I thank Byron Adams for generous use of his greenhouse and camera. I also thank (in no particular order) Aaron Weed, Jim Dunford, Katie Barbara, Erin Britton, Erin Gentry, Aissa Doumboya, Alison Neeley, Matthew Brightman, Scotty Long, Wade Davidson, Kelly Sims (Latsha), Jodi Avila, Matt Aubuchon, Emily Heffernan, Heather Smith, David Serrano, Susana Carrasco, Alejandro Arevalo and all of the other graduate students that kept me going and inspired about the work we have been doing. -
2009 01 CON ISBCA3 Copy COVER
BIOLOGICAL CONTROL OF COFFEE BERRY BORER: THE ROLE OF DNA-BASED GUT-CONTENT ANALYSIS IN ASSESSMENT OF PREDATION Eric G. Chapman1, Juliana Jaramillo2, 3, Fernando E. Vega4, & James D. Harwood1 1 Department of Entomology, University of Kentucky, S225 Agricultural Science Center North, Lexington KY 40546-0091, U.S.A., [email protected]; [email protected]; 2 International Center of Insect Physiology and Ecology (icipe) P.O.Box 30772-00100 Nairobi, Kenya. 3Institute of Plant Diseases and Plant Protection, University of Hannover, Herrenhäuser Strasse. 2, 30419 Hannover - Germany. [email protected]; 4Sustainable Perennial Crops Laboratory, U. S. Department of Agriculture, Agricultural Research Service, Building 001, Beltsville MD 20705, U.S.A. [email protected] ABSTRACT. The coffee berry borer, Hypothenemus hampei, is the most important pest of coffee worldwide, causing an estimated $500 million in damage annually. Infestation rates from 50-90% have been reported, significantly impacting coffee yields. Adult female H. hampei bore into the berry and lay eggs whose larvae hatch and spend their entire larval life within the berry, feeding on the coffee bean, lowering its quality and sometimes causing abscission. Biological control of H. hampei using parasitoids, fungi and nematodes has been reported but potential predators such as ants and predatory thrips, which have been observed in and around the coffee berries, have received little attention. This study reviews previous H. hampei biological control efforts and focuses on the role of predators in H. hampei biological control, an area in which tracking trophic associations by direct observation is not possible in part due to the cryptic nature of the biology of H. -
Thrips of California
BULLETIN OF THE CALIFORNIA INSECT SURVEY VOLUME 4, NO. 5 THE THRIPS OF CALIFORNIA PART I: SUBORDER TEREBRANTIA BY STANLEY F. BAILEY (Department of Entomology and Parasitology, University’ of California, Davis) UNIVERSITY OF CALIFORNIA PRESS BERKELEY AND LOS ANGELES 1957 BULLETIN OF THE CALIFORNIA INSECT SURVEY Editors: E. G. Linsley, S. B. Freeborn, P. D. Hurd, R. L. Usinger Volume 4, No. 5, pp. 143-220, plates 17-23 Submitted by Editors, March 28, 1956 Issued April 12, 1957 Price $1.50 UNIVERSITY OF CALIFORNIA PRESS BERKELEY AND LOS ANGELES CALIFORNIA CAMBRIDGE UNIVERSITY PRESS LONDON. ENGLAND PRINTED BY OFFSET IN THE UNITED STATES OF AMERICA CONTENTS Introduction ........................................................................... 143 Methods and Materials for the Collection of Thrips ........................................ 143 Bionomics ........................................................................... 145 Distribution ......................................................................... 145 Systematics ............................................................................ 146 Key to the Genera of California Thysanoptera: Terebrantia ................................. 147 Aeolothrips ........................................................................ 151 Anaphothrips ...................................................................... 159 Ankothrips ........................................................................ 163 Aptinothrips ......................................................................