Diptera: Tabanidae) of Jordan with Remarks on Ecology and Zoogeography
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Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016
Old Woman Creek National Estuarine Research Reserve Management Plan 2011-2016 April 1981 Revised, May 1982 2nd revision, April 1983 3rd revision, December 1999 4th revision, May 2011 Prepared for U.S. Department of Commerce Ohio Department of Natural Resources National Oceanic and Atmospheric Administration Division of Wildlife Office of Ocean and Coastal Resource Management 2045 Morse Road, Bldg. G Estuarine Reserves Division Columbus, Ohio 1305 East West Highway 43229-6693 Silver Spring, MD 20910 This management plan has been developed in accordance with NOAA regulations, including all provisions for public involvement. It is consistent with the congressional intent of Section 315 of the Coastal Zone Management Act of 1972, as amended, and the provisions of the Ohio Coastal Management Program. OWC NERR Management Plan, 2011 - 2016 Acknowledgements This management plan was prepared by the staff and Advisory Council of the Old Woman Creek National Estuarine Research Reserve (OWC NERR), in collaboration with the Ohio Department of Natural Resources-Division of Wildlife. Participants in the planning process included: Manager, Frank Lopez; Research Coordinator, Dr. David Klarer; Coastal Training Program Coordinator, Heather Elmer; Education Coordinator, Ann Keefe; Education Specialist Phoebe Van Zoest; and Office Assistant, Gloria Pasterak. Other Reserve staff including Dick Boyer and Marje Bernhardt contributed their expertise to numerous planning meetings. The Reserve is grateful for the input and recommendations provided by members of the Old Woman Creek NERR Advisory Council. The Reserve is appreciative of the review, guidance, and council of Division of Wildlife Executive Administrator Dave Scott and the mapping expertise of Keith Lott and the late Steve Barry. -
Diptera, Tabanoidea, Tabanidae) Dorian D
Dörge et al. Parasites Vectors (2020) 13:461 https://doi.org/10.1186/s13071-020-04316-7 Parasites & Vectors RESEARCH Open Access Incompletely observed: niche estimation for six frequent European horsefy species (Diptera, Tabanoidea, Tabanidae) Dorian D. Dörge1*, Sarah Cunze1 and Sven Klimpel1,2 Abstract Background: More than 170 species of tabanids are known in Europe, with many occurring only in limited areas or having become very rare in the last decades. They continue to spread various diseases in animals and are responsible for livestock losses in developing countries. The current monitoring and recording of horsefies is mainly conducted throughout central Europe, with varying degrees of frequency depending on the country. To the detriment of tabanid research, little cooperation exists between western European and Eurasian countries. Methods: For these reasons, we have compiled available sources in order to generate as complete a dataset as possi- ble of six horsefy species common in Europe. We chose Haematopota pluvialis, Chrysops relictus, C. caecutiens, Tabanus bromius, T. bovinus and T. sudeticus as ubiquitous and abundant species within Europe. The aim of this study is to esti- mate the distribution, land cover usage and niches of these species. We used a surface-range envelope (SRE) model in accordance with our hypothesis of an underestimated distribution based on Eurocentric monitoring regimes. Results: Our results show that all six species have a wide range in Eurasia, have a broad climatic niche and can there- fore be considered as widespread generalists. Areas with modelled habitat suitability cover the observed distribution and go far beyond these. This supports our assumption that the current state of tabanid monitoring and the recorded distribution signifcantly underestimates the actual distribution. -
Table of Contents 2
Southwest Association of Freshwater Invertebrate Taxonomists (SAFIT) List of Freshwater Macroinvertebrate Taxa from California and Adjacent States including Standard Taxonomic Effort Levels 1 March 2011 Austin Brady Richards and D. Christopher Rogers Table of Contents 2 1.0 Introduction 4 1.1 Acknowledgments 5 2.0 Standard Taxonomic Effort 5 2.1 Rules for Developing a Standard Taxonomic Effort Document 5 2.2 Changes from the Previous Version 6 2.3 The SAFIT Standard Taxonomic List 6 3.0 Methods and Materials 7 3.1 Habitat information 7 3.2 Geographic Scope 7 3.3 Abbreviations used in the STE List 8 3.4 Life Stage Terminology 8 4.0 Rare, Threatened and Endangered Species 8 5.0 Literature Cited 9 Appendix I. The SAFIT Standard Taxonomic Effort List 10 Phylum Silicea 11 Phylum Cnidaria 12 Phylum Platyhelminthes 14 Phylum Nemertea 15 Phylum Nemata 16 Phylum Nematomorpha 17 Phylum Entoprocta 18 Phylum Ectoprocta 19 Phylum Mollusca 20 Phylum Annelida 32 Class Hirudinea Class Branchiobdella Class Polychaeta Class Oligochaeta Phylum Arthropoda Subphylum Chelicerata, Subclass Acari 35 Subphylum Crustacea 47 Subphylum Hexapoda Class Collembola 69 Class Insecta Order Ephemeroptera 71 Order Odonata 95 Order Plecoptera 112 Order Hemiptera 126 Order Megaloptera 139 Order Neuroptera 141 Order Trichoptera 143 Order Lepidoptera 165 2 Order Coleoptera 167 Order Diptera 219 3 1.0 Introduction The Southwest Association of Freshwater Invertebrate Taxonomists (SAFIT) is charged through its charter to develop standardized levels for the taxonomic identification of aquatic macroinvertebrates in support of bioassessment. This document defines the standard levels of taxonomic effort (STE) for bioassessment data compatible with the Surface Water Ambient Monitoring Program (SWAMP) bioassessment protocols (Ode, 2007) or similar procedures. -
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. -
A New Synonymy in the Horsefly Genus Hybomitra (Diptera: Tabanidae)
a new synonymy in the horsefly genus HYBOMITRA (diptera: tabanidae) Theo Zeegers The taxonomy and nomenclature of Hybomitra solstitialis is critically revised. Based on a re-examination of the type, H. solstitialis is found to be identical with the species currently known as H. ciureai syn. nov. Since the 1950s the name H. solstitalis has been misinterpreted in European literature. This concept, introduced by Lyneborg, is shown to be a light coloured variety of H. bimaculata. introduction The horseflies (family Tabanidae) are a median The discovery by Lyneborg (15) of the impor- sized family (about 170 species in Europe, Chvála tance of the shape of the subgenital plate, espe- et al. (172)) of median to very large flies (6- cially in the H. bimaculata-group, was a major 25 mm). Females are notorious for sucking blood breakthrough in the taxonomy of the genus on both humans and livestock. In the palearctic Hybomitra. Unfortunately, he distinguished too region, the tribe Tabanini of the subfamily Taban- many species due to underestimating of the inae is the most abundant group of horseflies. colour variation. This was largely corrected by In the palearctic region the horsefly genera are Chvála et al. (172), introducing a system that has well defined. Identification of species is often been followed since (Moucha 176, Olsufjev 177, difficult due to variability in coloration and Trojan 17, Timmer 10, Chvála 1, Zeegers paucity of structural features. Identification is & Van Haaren 2000, Stubbs & Drake 2001, especially challenging in the genus Hybomitra Portillo 2002). Enderlein, 122, characterized by the presence of an ocellar tubercle on the vertex. -
Scottish Pollinating Flies
Scottish Pollinating Flies Introduction to True flies True flies form one of the largest and most diverse orders of insects called Diptera (meaning two wings). There are around 160,000 species worldwide in 150 families, with 7,200 species from over 90 families recorded in the UK. They inhabit every continent and almost every terrestrial and freshwater niche on the planet which is testament to their adaptability. True flies differ from other insects in that they have retained only their front pair of wings, with the hind pair having evolved into small club-shaped appendages called ‘halteres’ which act as gyroscopes and facilitate greater aerobatic agility. They provide a range of ecological services including pollination, controlling pest species, the decomposition of organic material, and supplementing the dietary requirements of a wide range of other organisms. Pollinating flies and other dipterans Of the four most significant orders of pollinating insects, flies are the most abundant. Approximately 1,500 of the 7,200 British species are thought to contribute to pollination. Hoverflies (family Syrphidae) are especially significant pollinators, but some other families (the house flies and their relatives) are just as important. The remainder of the 90+ families contribute relatively few, or no pollinating species. True flies contribute to more pollination in Scotland than any other order of insects, mainly due to the sparsity, absence or selectiveness of bees in colder, northern upland habitats. Below are some examples that demonstrate the diversity of true flies that may be encountered. Common dronefly (Eristalis tenax) Splayed deerfly Chrysops( caecutiens) © Steven Falk © Steven © Steven Falk © Steven Cranefly Tipula lateralis Orange-legged robberfly (Dioctria oelandica) © Steven Falk © Steven Falk © Steven Buglife—The Invertebrate Conservation Trust is a company limited by guarantee. -
The Status and Distribution of the Horseflies Atylotus Plebeius and Hybomitra Lurida on the Cheshire Plain Area of North West England
The status and distribution of the horseflies Atylotus plebeius and Hybomitra lurida on the Cheshire Plain area of North West England Including assessments of mire habitats and accounts of other horseflies (Tabanidae) Atylotus plebeius (Fallén) [Cheshire Horsefly]: male from Little Budworth Common 10th June 2018; female from Shemmy Moss 9th June 2018 A report to Gary Hedges, Tanyptera Regional Entomology Project Officer, Entomology, National Museums Liverpool, World Museum, William Brown Street, L3 8EN Email: [email protected] By entomological consultant Andrew Grayson, ‘Scardale’, High Lane, Beadlam, Nawton, York, YO62 7SX Email: [email protected] Based on The results of a survey carried out during 2018 Report submitted on 2nd March 2019 CONTENTS INTRODUCTION . 1 SUMMARY . 1 THE CHESHIRE PLAIN AREA MIRES . 1 HISTORICAL BACKGROUND TO ATYLOTUS PLEBEIUS IN THE CHESHIRE PLAIN AREA . 2 HISTORICAL BACKGROUND TO HYBOMITRA LURIDA IN THE CHESHIRE PLAIN AREA . 2 OTHER HORSEFLIES RECORDED IN THE CHESHIRE PLAIN AREA . 3 METHODOLOGY FOR THE 2018 SURVEY . 3 INTRODUCTION . 3 RECONNAISSANCE . 4 THE SURVEY . 4 LOCALITIES . 5 ABBOTS MOSS COMPLEX MIRES ON FOREST CAMP LAND . 5 ABBOTS MOSS COMPLEX MIRES ON FORESTRY COMMISSION LAND . 7 BRACKENHURST BOG AND NEWCHURCH COMMON . 8 DELAMERE FOREST MIRES . 9 LITTLE BUDWORTH COMMON MIRES . 17 PETTY POOL AREA WETLANDS . 18 MISCELLANEOUS DELAMERE AREA MIRES . 19 WYBUNBURY MOSS AND CHARTLEY MOSS . 21 BROWN MOSS . 22 CLAREPOOL MOSS AND COLE MERE . 23 THE FENN’S, WHIXALL, BETTISFIELD, WEM AND CADNEY MOSSES COMPLEX SSSI MIRES . 24 POTENTIAL HOST ANIMALS FOR FEMALE TABANIDAE BLOOD MEALS . 26 RESULTS . 27 TABANIDAE . 27 SUMMARY . 27 SPECIES ACCOUNTS . 27 TABLE SHOWING DISSECTION OF HORSEFLY NUMBERS . -
Checklist of Lithuanian Diptera
Acta Zoologica Lituanica. 2000. Volumen 10. Numerus 1 3 ISSN 1392-1657 CHECKLIST OF LITHUANIAN DIPTERA Saulius PAKALNIÐKIS1, Jolanta RIMÐAITË1, Rasa SPRANGAUSKAITË-BERNOTIENË1, Rasa BUTAUTAITË2, Sigitas PODËNAS2 1 Institute of Ecology, Akademijos 2, 2600 Vilnius, Lithuania 2 Department of Zoology, Vilnius University, M.K. Èiurlionio 21/27, 2009 Vilnius, Lithuania Abstract. The list of 2283 Lithuanian Diptera species of 78 families is based on 224 literary sources. Key words: Diptera, Acroceridae, Agromyzidae, Anisopodidae, Anthomyiidae, Anthomyzidae, Asilidae, Athericidae, Bibionidae, Bombyliidae, Calliphoridae, Cecidomyiidae, Ceratopogonidae, Chama- emyiidae, Chaoboridae, Chironomidae, Chloropidae, Coelopidae, Conopidae, Culicidae, Cylindroto- midae, Diastatidae, Ditomyiidae, Dixidae, Dolichopodidae, Drosophilidae, Dryomyzidae, Empididae, Ephydridae, Fanniidae, Gasterophilidae, Helcomyzidae, Heleomyzidae, Hippoboscidae, Hybotidae, Hypodermatidae, Lauxaniidae, Limoniidae, Lonchaeidae, Lonchopteridae, Macroceridae, Megamerinidae, Micropezidae, Microphoridae, Muscidae, Mycetophilidae, Neottiophilidae, Odiniidae, Oestridae, Opo- myzidae, Otitidae, Pallopteridae, Pediciidae, Phoridae, Pipunculidae, Platypezidae, Psilidae, Psychod- idae, Ptychopteridae, Rhagionidae, Sarcophagidae, Scathophagidae, Scatopsidae, Scenopinidae, Sciaridae, Sciomyzidae, Sepsidae, Simuliidae, Sphaeroceridae, Stratiomyidae, Syrphidae, Tabanidae, Tachinidae, Tephritidae, Therevidae, Tipulidae, Trichoceridae, Xylomyidae, Xylophagidae, checklist, Lithuania INTRODUCTION -
Diptera: Athericidae)
Boletín de la Sociedad Entomológica Aragonesa (S.E.A.), nº 54 (30/6/2014): 349–350. FIRST PORTUGUESE RECORD OF THE GENUS ATRICHOPS VERRALL (DIPTERA: ATHERICIDAE) Rui Andrade Rua Calouste Gulbenkian 237 4H3, Porto, Portugal – [email protected] Abstract: The dipteran family Athericidae is, in Portugal, insufficiently known with only one species recorded to date. In this paper, the species Atrichops crassipes (Meigen, 1820) is recorded for the first time in Portugal increasing the number of species of this family in the country from one to two. Key words: Diptera, Athericidae, Atrichops crassipes, new record, distribution, Portugal. Primera cita portuguesa del género Atrichops Verrall (Diptera: Athericidae). Resumen: La familia de dípteros Athericidae está insuficientemente conocida en Portugal, de donde se ha citado sólo una especie hasta ahora. En este trabajo, la especie Atrichops crassipes (Meigen, 1820) se cita por primera vez de Portugal, incrementando el número de especies de esta familia en el país de una a dos. Palabras clave: Diptera, Athericidae, Atrichops crassipes, cita nueva, distribución, Portugal. Athericidae (Diptera) is a small family of brachyceran flies The location where the single specimen was collected, related to the Tabanidae. The adults are medium sized with which is situated on the outskirts of the city of Valongo, suf- dark bodies often with transversely fasciate abdominal ter- fers from intense human pressure. The watercourses on the gites. The eyes in males nearly meet, while females are di- area are polluted and is common to find garbage along the choptic, and both have ocelli. Antenna is short with flagellum margins. The dominant tree species is the eucalyptus (Euca- reniform. -
New Records for the Horse Fly Fauna (Diptera: Tabanidae) of Jordan with Remarks on Ecology and Zoogeography
9ROQR -RXUQDORI9HFWRU(FRORJ\ New records for the horse fly fauna (Diptera: Tabanidae) of Jordan with remarks on ecology and zoogeography Günter C. Müller1 , Jerome A. Hogsette2, Edita E. Revay3, Vasiliy D. Kravchenko4, Andrey Leshvanov5, and Yosef Schlein1 1Department of Microbiology and Molecular Genetics, IMRIC, Kuvin Centre for the Study of Infectious and Tropical Diseases, Faculty of Medicine, Hebrew University, Jerusalem, Israel, 91120, [email protected] 2United States Department of Agriculture-ARS-Center for Medical, Agricultural, and Veterinary Entomology, Gainesville, FL, U.S.A. 3Department of Anatomy and Cell Biology, Bruce Rappaport Faculty of Medicine, Technion, Haifa, Israel 4Department of Zoology, Tel Aviv University, Tel Aviv, Israel 5Department of Zoology, Ulyanovsk State Pedagogical University, 432600, Russia Received 4 August 2011; Accepted 5 September 2011 ABSTRACT: The horse fly fauna (Diptera: Tabanidae) of Jordan is, after Israel, the richest in the Levant, with 24 known species. During the 20-year project “The Ecology and Zoogeography of the Lepidoptera of the Near East,” we regularly collected blood-feeding flies, resulting in 11 additional species of Tabanidae for Jordan. The new records are: Atylotus quadrifarius (Loew, 1874), Chrysops caecutiens (Linnaeus, 1758), Dasyrhamphis nigritus (Fabricius, 1794), Haematopota pallens Loew, 1871, Nemorius irritans (Ricardo, 1901), Philipomyia graeca (Fabricius, 1794), Tabanus cordiger Meigen, 1820, Tabanus taeniola Palisot de Beauvois, 1806, Tabanus quatuornotatus Meigen, 1820, Tabanus separatus Effllatoun, 1930, and Tabanus spectabilis Loew, 1858. Most of the new records (10/11) are of Palearctic origin; of these, six are of a Mediterranean and one each of West Palearctic, Euroasiatic, Irano-Turanian, and Eremic providence. Only one species, T. -
The Wing Stalk in Diptera, with Some Notes on the Higher-Level Phylogeny of the Order
POINT OF VIEW Eur. J. Entomol. 105: 27–33, 2008 http://www.eje.cz/scripts/viewabstract.php?abstract=1297 ISSN 1210-5759 (print), 1802-8829 (online) The wing stalk in Diptera, with some notes on the higher-level phylogeny of the order JAROSLAV STARÝ Department of Zoology and Laboratory of Ornithology, Faculty of Science of the Palacký University, tĜ. Svobody 26, 771 46 Olomouc, Czech Republic; e-mail: [email protected] Key words. Diptera, morphology, wing stalk, higher-level phylogeny Abstract. The wing stalk in Diptera is examined, and its structures are re-evaluated and re-interpreted. The non-homology of A2 in Tipulomorpha and “A2” in other Diptera is claimed. Some notes are presented on the higher-level phylogeny of Diptera, especially those concerning Tipulomorpha. The family Trichoceridae is restored among Tipulomorpha, and the Tipulomorpha are re-affirmed as the sister group of the remaining Diptera. The clade Anisopodidae + Culicomorpha + Bibionomorpha is suggested as the sister group of Brachycera. INTRODUCTION chodomorpha, and particular taxa are treated at family Hennig (1968) published a comprehensive treatment of level. The infraorders accepted are conceived here as fol- the evolution of the wing base in Diptera, i.e., the com- lows: Tipulomorpha: Trichoceridae, Limoniidae, Pedicii- plex of features within the so-called wing stalk, mainly dae, Tipulidae, Cylindrotomidae; Culicomorpha: Simuli- idae, Dixidae, Culicidae, Thaumaleidae, Ceratopogon- the reduction of A2 and the development of the alula. He idae, Chironomidae; Bibionomorpha: Cecidomyiidae, concluded that A2 is reduced in Diptera other than Tipulo- morpha and only retained as a more or less sclerotised, Bibionidae, Axymyiidae, Mycetophilidae s. -
Diptera – Brachycera
Biodiversity Data Journal 3: e4187 doi: 10.3897/BDJ.3.e4187 Data Paper Fauna Europaea: Diptera – Brachycera Thomas Pape‡§, Paul Beuk , Adrian Charles Pont|, Anatole I. Shatalkin¶, Andrey L. Ozerov¶, Andrzej J. Woźnica#, Bernhard Merz¤, Cezary Bystrowski«», Chris Raper , Christer Bergström˄, Christian Kehlmaier˅, David K. Clements¦, David Greathead†,ˀ, Elena Petrovna Kamenevaˁ, Emilia Nartshuk₵, Frederik T. Petersenℓ, Gisela Weber ₰, Gerhard Bächli₱, Fritz Geller-Grimm₳, Guy Van de Weyer₴, Hans-Peter Tschorsnig₣, Herman de Jong₮, Jan-Willem van Zuijlen₦, Jaromír Vaňhara₭, Jindřich Roháček₲, Joachim Ziegler‽, József Majer ₩, Karel Hůrka†,₸, Kevin Holston ‡‡, Knut Rognes§§, Lita Greve-Jensen||, Lorenzo Munari¶¶, Marc de Meyer##, Marc Pollet ¤¤, Martin C. D. Speight««, Martin John Ebejer»», Michel Martinez˄˄, Miguel Carles-Tolrá˅˅, Mihály Földvári¦¦, Milan Chvála ₸, Miroslav Bartákˀˀ, Neal L. Evenhuisˁˁ, Peter J. Chandler₵₵, Pierfilippo Cerrettiℓℓ, Rudolf Meier ₰₰, Rudolf Rozkosny₭, Sabine Prescher₰, Stephen D. Gaimari₱₱, Tadeusz Zatwarnicki₳₳, Theo Zeegers₴₴, Torsten Dikow₣₣, Valery A. Korneyevˁ, Vera Andreevna Richter†,₵, Verner Michelsen‡, Vitali N. Tanasijtshuk₵, Wayne N. Mathis₣₣, Zdravko Hubenov₮₮, Yde de Jong ₦₦,₭₭ ‡ Natural History Museum of Denmark, Copenhagen, Denmark § Natural History Museum Maastricht / Diptera.info, Maastricht, Netherlands | Oxford University Museum of Natural History, Oxford, United Kingdom ¶ Zoological Museum, Moscow State University, Moscow, Russia # Wrocław University of Environmental and Life Sciences, Wrocław,