Phorid Newsletter #5
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Rediscovery and Reclassification of the Dipteran Taxon Nothomicrodon
www.nature.com/scientificreports OPEN Rediscovery and reclassification of the dipteran taxon Nothomicrodon Wheeler, an exclusive Received: 07 November 2016 Accepted: 28 February 2017 endoparasitoid of gyne ant larvae Published: 31 March 2017 Gabriela Pérez-Lachaud1, Benoit J. B. Jahyny2,3, Gunilla Ståhls4, Graham Rotheray5, Jacques H. C. Delabie6 & Jean-Paul Lachaud1,7 The myrmecophile larva of the dipteran taxon Nothomicrodon Wheeler is rediscovered, almost a century after its original description and unique report. The systematic position of this dipteran has remained enigmatic due to the absence of reared imagos to confirm indentity. We also failed to rear imagos, but we scrutinized entire nests of the Brazilian arboreal dolichoderine ant Azteca chartifex which, combined with morphological and molecular studies, enabled us to establish beyond doubt that Nothomicrodon belongs to the Phoridae (Insecta: Diptera), not the Syrphidae where it was first placed, and that the species we studied is an endoparasitoid of the larvae of A. chartifex, exclusively attacking sexual female (gyne) larvae. Northomicrodon parasitism can exert high fitness costs to a host colony. Our discovery adds one more case to the growing number of phorid taxa known to parasitize ant larvae and suggests that many others remain to be discovered. Our findings and literature review confirm that the Phoridae is the only taxon known that parasitizes both adults and the immature stages of different castes of ants, thus threatening ants on all fronts. Ants are hosts to at least 17 orders of myrmecophilous arthropods (organisms dependent on ants), ranging from general scavengers to highly selective predators and parasitoids that attack either ants, their brood or other myr- mecophiles1–3. -
Diptera, Phoridae) from Iran
Archive of SID J Insect Biodivers Syst 04(3): 147–155 ISSN: 2423-8112 JOURNAL OF INSECT BIODIVERSITY AND SYSTEMATICS Research Article http://jibs.modares.ac.ir http://zoobank.org/References/578CCEF1-37B7-45D3-9696-82B159F75BEB New records of the scuttle flies (Diptera, Phoridae) from Iran Roya Namaki Khameneh1, Samad Khaghaninia1*, R. Henry L. Disney2 1 Department of Plant Protection, Faculty of Agriculture, University of Tabriz, Tabriz, I.R. Iran. 2 Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, U.K. ABSTRACT. The faunistic study of the family Phoridae carried out in northwestern of Iran during 2013–2017. Five species (Conicera tibialis Schmitz, Received: 1925, Dohrniphora cornuta (Bigot, 1857), Gymnophora arcuata (Meigen, 1830), 06 August, 2018 Metopina oligoneura (Mik, 1867) and Triphleba intermedia (Malloch, 1908)) are newly recorded from Iran. The genera Conicera Meigen, 1830, Dohrniphora Accepted: 14 November, 2018 Dahl, 1898, Gymnophora Macquart, 1835 and Triphleba Rondani, 1856 are reported for the first time from the country. Diagnostic characters of the Published: studied species along with their photographs are provided. 20 November, 2018 Subject Editor: Key words: Phoridae, Conicera, Dohrniphora, Gymnophora, Triphleba, Iran, New Farzaneh Kazerani records Citation: Namaki khameneh, R., Khaghaninia, S. & Disney, R.H.L. (2018) New records of the scuttle flies (Diptera, Phoridae) from Iran. Journal of Insect Biodiversity and Systematics, 4 (3), 147–155. Introduction Phoridae with about 4,000 identified insect eggs, larvae, and pupae. The adults species in more than 260 genera, is usually feed on nectar, honeydew and the considered as one of the largest families of exudates of fresh carrion and dung, Diptera (Ament & Brown, 2016). -
Diptera) Diversity in a Patch of Costa Rican Cloud Forest: Why Inventory Is a Vital Science
Zootaxa 4402 (1): 053–090 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2018 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4402.1.3 http://zoobank.org/urn:lsid:zoobank.org:pub:C2FAF702-664B-4E21-B4AE-404F85210A12 Remarkable fly (Diptera) diversity in a patch of Costa Rican cloud forest: Why inventory is a vital science ART BORKENT1, BRIAN V. BROWN2, PETER H. ADLER3, DALTON DE SOUZA AMORIM4, KEVIN BARBER5, DANIEL BICKEL6, STEPHANIE BOUCHER7, SCOTT E. BROOKS8, JOHN BURGER9, Z.L. BURINGTON10, RENATO S. CAPELLARI11, DANIEL N.R. COSTA12, JEFFREY M. CUMMING8, GREG CURLER13, CARL W. DICK14, J.H. EPLER15, ERIC FISHER16, STEPHEN D. GAIMARI17, JON GELHAUS18, DAVID A. GRIMALDI19, JOHN HASH20, MARTIN HAUSER17, HEIKKI HIPPA21, SERGIO IBÁÑEZ- BERNAL22, MATHIAS JASCHHOF23, ELENA P. KAMENEVA24, PETER H. KERR17, VALERY KORNEYEV24, CHESLAVO A. KORYTKOWSKI†, GIAR-ANN KUNG2, GUNNAR MIKALSEN KVIFTE25, OWEN LONSDALE26, STEPHEN A. MARSHALL27, WAYNE N. MATHIS28, VERNER MICHELSEN29, STEFAN NAGLIS30, ALLEN L. NORRBOM31, STEVEN PAIERO27, THOMAS PAPE32, ALESSANDRE PEREIRA- COLAVITE33, MARC POLLET34, SABRINA ROCHEFORT7, ALESSANDRA RUNG17, JUSTIN B. RUNYON35, JADE SAVAGE36, VERA C. SILVA37, BRADLEY J. SINCLAIR38, JEFFREY H. SKEVINGTON8, JOHN O. STIREMAN III10, JOHN SWANN39, PEKKA VILKAMAA40, TERRY WHEELER††, TERRY WHITWORTH41, MARIA WONG2, D. MONTY WOOD8, NORMAN WOODLEY42, TIFFANY YAU27, THOMAS J. ZAVORTINK43 & MANUEL A. ZUMBADO44 †—deceased. Formerly with the Universidad de Panama ††—deceased. Formerly at McGill University, Canada 1. Research Associate, Royal British Columbia Museum and the American Museum of Natural History, 691-8th Ave. SE, Salmon Arm, BC, V1E 2C2, Canada. Email: [email protected] 2. -
Chapter 13. Assessing Host Specificity and Field Release Potential of Fire Ant Decapitating Flies (Phoridae: Pseudacteon)
ASSESSING HOST RANGES OF PARASITOIDS AND PREDATORS _________________________________ CHAPTER 13. ASSESSING HOST SPECIFICITY AND FIELD RELEASE POTENTIAL OF FIRE ANT DECAPITATING FLIES (PHORIDAE: PSEUDACTEON) S. D. Porter1 and L. E. Gilbert2 1USDA-ARS, Center for Medical, Agricultural and Veterinary Entomology, P.O. Box 14565, Gainesville, Florida 32604 USA [email protected] 2Brackenridge Field Laboratory and Section of Integrative Biology, University of Texas, Austin, Texas 78712 USA BACKGROUND OF SYSTEM Fire ant populations in their South American homeland are about 1/5 to 1/10 as dense as popu- lations in North America (Porter et al., 1992; Porter et al., 1997a). This intercontinental differ- ence in fire ant densities was not explained by differences in climate, habitat, soil type, land use, plant cover, or sampling protocols (Porter et al., 1997a). Escape from numerous natural en- emies left behind in South America is the most apparent explanation for the intercontinental population differences. Natural enemies left behind in South America include two species of microsporidian pathogens, three species of nematodes, about 20 species of phorid decapitating flies, a eucharitid wasp, a parasitic ant, and numerous other microbes and arthropods of uncer- tain relationship to fire ants (Porter et al., 1997a). Escape from coevolved ant communities may also have been important. Ants in Brazil and Argentina, however, do not appear to be any more abundant than those in the United States, at least as indicated by their ability to find and occupy baits (Porter et al., 1997a). Classical or self-sustaining biological control agents are currently the only potential means for achieving permanent regional control of fire ants. -
Bee Viruses: Routes of Infection in Hymenoptera
fmicb-11-00943 May 27, 2020 Time: 14:39 # 1 REVIEW published: 28 May 2020 doi: 10.3389/fmicb.2020.00943 Bee Viruses: Routes of Infection in Hymenoptera Orlando Yañez1,2*, Niels Piot3, Anne Dalmon4, Joachim R. de Miranda5, Panuwan Chantawannakul6,7, Delphine Panziera8,9, Esmaeil Amiri10,11, Guy Smagghe3, Declan Schroeder12,13 and Nor Chejanovsky14* 1 Institute of Bee Health, Vetsuisse Faculty, University of Bern, Bern, Switzerland, 2 Agroscope, Swiss Bee Research Centre, Bern, Switzerland, 3 Laboratory of Agrozoology, Department of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium, 4 INRAE, Unité de Recherche Abeilles et Environnement, Avignon, France, 5 Department of Ecology, Swedish University of Agricultural Sciences, Uppsala, Sweden, 6 Environmental Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand, 7 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand, 8 General Zoology, Institute for Biology, Martin-Luther-University of Halle-Wittenberg, Halle (Saale), Germany, 9 Halle-Jena-Leipzig, German Centre for Integrative Biodiversity Research (iDiv), Leipzig, Germany, 10 Department of Biology, University of North Carolina at Greensboro, Greensboro, NC, United States, 11 Department Edited by: of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, United States, 12 Department of Veterinary Akio Adachi, Population Medicine, College of Veterinary Medicine, University of Minnesota, Saint Paul, MN, United States, -
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). -
A Molecular Diagnostic Survey of Pathogens and Parasites of Honey Bees, Apis Mellifera L., from Arkansas and Oklahoma
University of Arkansas, Fayetteville ScholarWorks@UARK Theses and Dissertations 12-2017 A Molecular Diagnostic Survey of Pathogens and Parasites of Honey Bees, Apis mellifera L., From Arkansas and Oklahoma Dylan Cleary University of Arkansas, Fayetteville Follow this and additional works at: http://scholarworks.uark.edu/etd Part of the Entomology Commons, and the Parasitology Commons Recommended Citation Cleary, Dylan, "A Molecular Diagnostic Survey of Pathogens and Parasites of Honey Bees, Apis mellifera L., From Arkansas and Oklahoma" (2017). Theses and Dissertations. 2554. http://scholarworks.uark.edu/etd/2554 This Thesis is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. A Molecular Diagnostic Survey of Pathogens and Parasites of Honey Bees, Apis mellifera L., From Arkansas and Oklahoma A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology by Dylan Alexandra Cleary Oklahoma State University Bachelor of Science in Natural Resources, Ecology and Management, 2013 December 2017 University of Arkansas This thesis is approved for recommendation to the Graduate Council _____________________________ Allen L. Szalanski, Ph.D Thesis Director _____________________________ _____________________________ Donald Steinkraus, Ph.D Jackie Lee, Ph.D Co-Advisor Committee Member Abstract The health and viability of colonies of the honey bee, Apis mellifera, in the United States have fluctuated dramatically over the past decade. This poses a substantial threat to agricultural production in this country. Currently, no single factor has been identified for this decline. -
Insect Timing and Succession on Buried Carrion in East Lansing, Michigan
INSECT TIMING AND SUCCESSION ON BURIED CARRION IN EAST LANSING, MICHIGAN By Emily Christine Pastula A THESIS Submitted to Michigan State University in partial fulfillment of the requirements for the degree of MASTERS OF SCIENCE Entomology 2012 ABSTRACT INSECT TIMING AND SUCCESSION ON BURIED CARRION IN EAST LANSING, MICHIGAN By Emily Christine Pastula This study examined pig carcasses buried at two different depths, 30 and 60 cm, to determine if insects are able to colonize buried carcasses, when they arrive at each depth, and what fauna are present over seven sampling dates to establish an insect succession database on buried carrion in East Lansing, Michigan. Thirty-eight pigs were buried, 18 at 30 cm and 20 at 60 cm. Four control carcasses were placed on the soil surface. Three replicates at each depth were exhumed after 3 days, 7 days, 14 days, 21 days, 30 days, and 60 days. One pig was also exhumed from 60 cm after 90 days and another after 120 days. Sarcophaga bullata (Diptera: Sarcophagidae) and Hydrotaea sp. (Diptera: Muscidae) were found colonizing buried carrion 5 days after burial at 30 cm. Insect succession at 30 cm proceeded with flesh and muscid flies being the first to colonize, followed by blow flies. Insects were able to colonize carcasses at 60 cm and Hydrotaea sp. and Megaselia scalaris (Diptera: Phoridae), were collected 7 days after burial. Insect succession at 60 cm did not proceed similarly as predicted, instead muscid and coffin flies were the only larvae collected. Overall these results reveal post-burial interval (PBI) estimates for forensic investigations in mid-Michigan during the summer, depending on climatic and soil conditions. -
INSECTS of MICRONESIA Diptera: Phoridae
INSECTS OF MICRONESIA Diptera: Phoridae By ERWIN M. BEYER BONN, STIFTSGASSE 8, WEST GERMANY INTRODUCTION G. E. Bohart was the first to report on phorids of Micronesia. In his study on the Phoridae of Guam [1947, U. S. Nat. Mus., Proc. 96 (3205): 397-416, figs. 33-48] he dealt with five genera and 11 species; one genus (Para fannia Bohart) and nine species were described as new. C. N. Colyer [1957, Hawaiian Ent. Soc., Proc. 16 (2) : 232] synonymized Parafannia Bohart with Gymnoptera Lioy. In our recent study on the Phoridae of Hawaii (Insects of Hawaii 11, 1964) D. E. Hardy and I recognize M egaselia stuntzi Bohart as a synonym of M. setaria (Malloch). In this present study, Pulici phora nigriventris Bohart is shown to be a synonym of P. pulex Dahl. Bohart's descriptions of his new species are inadequate and not always based upon the most reliable characters; the illustrations are sometimes inac curate. I am unable, therefore, to include Chonocephalus species in this study. In the Micronesian material before me, three members of this genus are rep resented; none of these can, however, be identified as any of Bohart's species. M egaselia setifemur Bohart, which also needs redescription, is not repre sented in this material. At present, seven genera, two subgenera, and 24 named species of Phori dae, including the two species of ChonocephalusJ are known to occur in Micro nesia. Ten species are new to science, one tribe (Beckerinini) and five species are recorded for the first time in Micronesia. When considering the Micronesian phorid genera, it is evident that only genera of worldwide distribution are represented. -
Georg-August-Universität Göttingen
GÖTTINGER ZENTRUM FÜR BIODIVERSITÄTSFORSCHUNG UND ÖKOLOGIE GÖTTINGEN CENTRE FOR BIODIVERSITY AND ECOLOGY Herb layer characteristics, fly communities and trophic interactions along a gradient of tree and herb diversity in a temperate deciduous forest Dissertation zur Erlangung des Doktorgrades der Mathematisch-Naturwissenschaftlichen Fakultäten der Georg-August-Universität Göttingen vorgelegt von Mag. rer. nat. Elke Andrea Vockenhuber aus Wien Göttingen, Juli, 2011 Referent: Prof. Dr. Teja Tscharntke Korreferent: Prof. Dr. Stefan Vidal Tag der mündlichen Prüfung: 16.08.2011 2 CONTENTS Chapter 1: General Introduction............................................................................................ 5 Effects of plant diversity on ecosystem functioning and higher trophic levels ....................................................... 6 Study objectives and chapter outline ...................................................................................................................... 8 Study site and study design ................................................................................................................................... 11 Major hypotheses.................................................................................................................................................. 12 References............................................................................................................................................................. 13 Chapter 2: Tree diversity and environmental context -
Surveying for Terrestrial Arthropods (Insects and Relatives) Occurring Within the Kahului Airport Environs, Maui, Hawai‘I: Synthesis Report
Surveying for Terrestrial Arthropods (Insects and Relatives) Occurring within the Kahului Airport Environs, Maui, Hawai‘i: Synthesis Report Prepared by Francis G. Howarth, David J. Preston, and Richard Pyle Honolulu, Hawaii January 2012 Surveying for Terrestrial Arthropods (Insects and Relatives) Occurring within the Kahului Airport Environs, Maui, Hawai‘i: Synthesis Report Francis G. Howarth, David J. Preston, and Richard Pyle Hawaii Biological Survey Bishop Museum Honolulu, Hawai‘i 96817 USA Prepared for EKNA Services Inc. 615 Pi‘ikoi Street, Suite 300 Honolulu, Hawai‘i 96814 and State of Hawaii, Department of Transportation, Airports Division Bishop Museum Technical Report 58 Honolulu, Hawaii January 2012 Bishop Museum Press 1525 Bernice Street Honolulu, Hawai‘i Copyright 2012 Bishop Museum All Rights Reserved Printed in the United States of America ISSN 1085-455X Contribution No. 2012 001 to the Hawaii Biological Survey COVER Adult male Hawaiian long-horned wood-borer, Plagithmysus kahului, on its host plant Chenopodium oahuense. This species is endemic to lowland Maui and was discovered during the arthropod surveys. Photograph by Forest and Kim Starr, Makawao, Maui. Used with permission. Hawaii Biological Report on Monitoring Arthropods within Kahului Airport Environs, Synthesis TABLE OF CONTENTS Table of Contents …………….......................................................……………...........……………..…..….i. Executive Summary …….....................................................…………………...........……………..…..….1 Introduction ..................................................................………………………...........……………..…..….4 -
Parasite Interactions in Urban Gardens
Environmental Entomology, XX(X), 2017, 1–9 doi: 10.1093/ee/nvx155 Research Pollinator Ecology and Management Vegetation Management and Host Density Influence Bee– Parasite Interactions in Urban Gardens Hamutahl Cohen,1,2,3 Robyn D. Quistberg,1 and Stacy M. Philpott1 1Environmental Studies Department, University of California, Santa Cruz, CA 95064, 2Environmental Studies Department, University of California, 1156 High Street, Santa Cruz, CA 95060, and 3Corresponding author, e-mail: [email protected] Subject Editor: Gloria DeGrandi-Hoffman Received 17 April 2017; Editorial decision 28 August 2017 Abstract Apocephalus borealis phorid flies, a parasitoid of bumble bees and yellow jacket wasps in North America, was recently reported as a novel parasitoid of the honey bee Apis mellifera Linnaeus (Hymenoptera: Apidae). Little is known about the ecology of this interaction, including phorid fecundity on bee hosts, whether phorid-bee parasitism is density dependent, and which local habitat and landscape features may correlate with changes in parasitism rates for either bumble or honey bees. We examined the impact of local and landscape drivers and host abundance on phorid parasitism of A. mellifera and the bumble bee Bombus vosnesenskii Radoszkowski (Hymenoptera: Apidae). We worked in 19 urban gardens along the North-Central Coast of California, where phorid parasitism of honey bees was first reported in 2012. We collected and incubated bees for phorid emergence, and surveyed local vegetation, ground cover, and floral characteristics as well as land cover types surrounding gardens. We found that phorid parasitism was higher on bumble bees than on honey bees, and phorids produced nearly twice as many pupae on individual bumble bee hosts than on honey bee hosts.