View the PDF File of Supplement

Total Page:16

File Type:pdf, Size:1020Kb

View the PDF File of Supplement Diptera types in the Supplement Canadian National Edition 4.0 Collection of Insects Diptera types in the Supplement Canadian National Edition 4.0 Collection of Insects Scott E. Brooks, Bradley J. Sinclair, Jeffrey M. Cumming, James E. O’Hara, Jeffrey H. Skevington, Owen Lonsdale and Bruce E. Cooper Invertebrate Biodiversity Agriculture and Agri-Food Canada Ottawa, Ontario K1A 0C6 February 24, 2015 Cover illustration Hemerodromia rogatoris Coquillett DIPTERA TYPES IN THE CNC: SUPPLEMENT 3 CONTENTS Introduction ...................................................................................................................................... 6 Agromyzidae .................................................................................................................................... 7 Anthomyiidae ................................................................................................................................... 7 Anthomyzidae ................................................................................................................................ 10 Asilidae .......................................................................................................................................... 10 Asteiidae ........................................................................................................................................ 11 Atelestidae ..................................................................................................................................... 11 Axymyiidae .................................................................................................................................... 11 Bibionidae ...................................................................................................................................... 12 Blephariceridae .............................................................................................................................. 12 Bombyliidae ................................................................................................................................... 12 Brachystomatidae ........................................................................................................................... 14 Calliphoridae .................................................................................................................................. 14 Camillidae ...................................................................................................................................... 14 Canacidae ....................................................................................................................................... 14 Carnidae ......................................................................................................................................... 15 Cecidomyiidae ............................................................................................................................... 15 Ceratopogonidae ............................................................................................................................ 16 Chamaemyiidae .............................................................................................................................. 21 Chironomidae ................................................................................................................................. 22 Chloropidae .................................................................................................................................... 25 Clusiidae ........................................................................................................................................ 26 Conopidae ...................................................................................................................................... 28 Corethrellidae ................................................................................................................................. 28 Ctenostylidae.................................................................................................................................. 30 Diastatidae ..................................................................................................................................... 30 Dixidae .......................................................................................................................................... 30 Dolichopodidae .............................................................................................................................. 30 Drosophilidae ................................................................................................................................. 35 Empididae ...................................................................................................................................... 35 DIPTERA TYPES IN THE CNC: SUPPLEMENT 4 Empidoidea Incertae sedis ............................................................................................................. 41 Heleomyzidae ................................................................................................................................ 42 Hilarimorphidae ............................................................................................................................. 43 Hippoboscidae ................................................................................................................................ 43 Hybotidae ....................................................................................................................................... 43 Inbiomyiidae .................................................................................................................................. 44 Ironomyiidae .................................................................................................................................. 45 Keroplatidae ................................................................................................................................... 45 Lauxaniidae .................................................................................................................................... 45 Limoniidae ..................................................................................................................................... 45 Lonchopteridae .............................................................................................................................. 45 Milichiidae ..................................................................................................................................... 45 Muscidae ........................................................................................................................................ 46 Mycetophilidae .............................................................................................................................. 46 Mythicomyiidae ............................................................................................................................. 51 Oreoleptidae ................................................................................................................................... 51 Paraleucopidae ............................................................................................................................... 51 Phoridae ......................................................................................................................................... 52 Piophilidae ..................................................................................................................................... 53 Pipunculidae .................................................................................................................................. 53 Rhinophoridae ................................................................................................................................ 54 Sarcophagidae ................................................................................................................................ 55 Scathophagidae .............................................................................................................................. 55 Sciaridae ......................................................................................................................................... 55 Sciomyzidae ................................................................................................................................... 57 Simuliidae ...................................................................................................................................... 57 Sphaeroceridae ............................................................................................................................... 59 Stratiomyidae ................................................................................................................................. 63 Strongylopthalmiidae ..................................................................................................................... 64 Syrphidae ....................................................................................................................................... 64 Tabanidae ....................................................................................................................................... 68 Tachinidae .....................................................................................................................................
Recommended publications
  • Insect Orders V: Panorpida & Hymenoptera
    Insect Orders V: Panorpida & Hymenoptera • The Panorpida contain 5 orders: the Mecoptera, Siphonaptera, Diptera, Trichoptera and Lepidoptera. • Available evidence clearly indicates that the Lepidoptera and the Trichoptera are sister groups. • The Siphonaptera and Mecoptera are also closely related but it is not clear whether the Siponaptera is the sister group of all of the Mecoptera or a group (Boreidae) within the Mecoptera. If the latter is true, then the Mecoptera is paraphyletic as currently defined. • The Diptera is the sister group of the Siphonaptera + Mecoptera and together make up the Mecopteroids. • The Hymenoptera does not appear to be closely related to any of the other holometabolous orders. Mecoptera (Scorpionflies, hangingflies) • Classification. 600 species worldwide, arranged into 9 families (5 in the US). A very old group, many fossils from the Permian (260 mya) onward. • Structure. Most distinctive feature is the elongated clypeus and labrum that together form a rostrum. The order gets its common name from the gential segment of the male in the family Panorpodiae, which is bulbous and often curved forward above the abdomen, like the sting of a scorpion. Larvae are caterpillar-like or grub- like. • Natural history. Scorpionflies are most common in cool, moist habitats. They get the name “hangingflies” from their habit of hanging upside down on vegetation. Larvae and adult males are mostly predators or scavengers. Adult females are usually scavengers. Larvae and adults in some groups may feed on vegetation. Larvae of most species are terrestrial and caterpillar-like in body form. Larvae of some species are aquatic. In the family Bittacidae males attract females for mating by releasing a sex pheromone and then presenting the female with a nuptial gift.
    [Show full text]
  • Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(S): Diego J
    Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(s): Diego J. Inclan and John O. Stireman, III Source: Annals of the Entomological Society of America, 104(2):287-296. Published By: Entomological Society of America https://doi.org/10.1603/AN10047 URL: http://www.bioone.org/doi/full/10.1603/AN10047 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. CONSERVATION BIOLOGY AND BIODIVERSITY Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States 1 DIEGO J. INCLAN AND JOHN O. STIREMAN, III Department of Biological Sciences, 3640 Colonel Glenn Highway, 235A, BH, Wright State University, Dayton, OH 45435 Ann. Entomol. Soc. Am. 104(2): 287Ð296 (2011); DOI: 10.1603/AN10047 ABSTRACT Although tachinids are one of the most diverse families of Diptera and represent the largest group of nonhymenopteran parasitoids, their local diversity and distribution patterns of most species in the family are poorly known.
    [Show full text]
  • CHIRONOMUS Newsletter on Chironomidae Research
    CHIRONOMUS Newsletter on Chironomidae Research No. 25 ISSN 0172-1941 (printed) 1891-5426 (online) November 2012 CONTENTS Editorial: Inventories - What are they good for? 3 Dr. William P. Coffman: Celebrating 50 years of research on Chironomidae 4 Dear Sepp! 9 Dr. Marta Margreiter-Kownacka 14 Current Research Sharma, S. et al. Chironomidae (Diptera) in the Himalayan Lakes - A study of sub- fossil assemblages in the sediments of two high altitude lakes from Nepal 15 Krosch, M. et al. Non-destructive DNA extraction from Chironomidae, including fragile pupal exuviae, extends analysable collections and enhances vouchering 22 Martin, J. Kiefferulus barbitarsis (Kieffer, 1911) and Kiefferulus tainanus (Kieffer, 1912) are distinct species 28 Short Communications An easy to make and simple designed rearing apparatus for Chironomidae 33 Some proposed emendations to larval morphology terminology 35 Chironomids in Quaternary permafrost deposits in the Siberian Arctic 39 New books, resources and announcements 43 Finnish Chironomidae 47 Chironomini indet. (Paratendipes?) from La Selva Biological Station, Costa Rica. Photo by Carlos de la Rosa. CHIRONOMUS Newsletter on Chironomidae Research Editors Torbjørn EKREM, Museum of Natural History and Archaeology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway Peter H. LANGTON, 16, Irish Society Court, Coleraine, Co. Londonderry, Northern Ireland BT52 1GX The CHIRONOMUS Newsletter on Chironomidae Research is devoted to all aspects of chironomid research and aims to be an updated news bulletin for the Chironomidae research community. The newsletter is published yearly in October/November, is open access, and can be downloaded free from this website: http:// www.ntnu.no/ojs/index.php/chironomus. Publisher is the Museum of Natural History and Archaeology at the Norwegian University of Science and Technology in Trondheim, Norway.
    [Show full text]
  • Diptera, Dolichopodidae) from Laos
    ISSN 1211-8788 Acta Musei Moraviae, Scientiae biologicae (Brno) 90: 247–250, 2005 Naticornus, a new genus of Neurigoninae (Diptera, Dolichopodidae) from Laos JIØÍ OLEJNÍÈEK Institute of Parasitology, Academy of Sciences of the Czech Republic, Branišovská 31, 370 05 Èeské Budìjovice, Czech Republic; e-mail: [email protected] OLEJNÍÈEK J. 2005: Naticornus, a new genus of Neurigoninae (Diptera, Dolichopodidae) from Laos. Acta Musei Moraviae, Scientiae biologicae (Brno) 90: 247–250. – Naticornus luteum gen.nov., sp.nov. is described from Laos. The new genus is characterized by conspicuously formed fifth abdominal tergite bearing a long horn in the male. Key to Oriental genera of Neurigoninae is appended. Key words. Dolichopodidae, Naticornus luteum, new genus, new species, Laos Introduction The subfamily Neurigoninae contained to date two genera in the Oriental region. DYTE (1975) recorded 12 species of the cosmopolitan genus Neurigona Rondani, 1856 and one undescribed species of Tenuopus Curran, 1924. Several species of Neurigona were described from China by YANG (1999); some of them may be common for both the Palaearctic and Oriental regions. The species of this subfamily are characterised above all by mostly yellow coloration, dorsal postcranium flat, thorax with strongly flattened posterior scope, proepisternum with setae, femora without praeapical bristles and by relatively large hypopygium (BICKEL 1998). The subfamily is much richer in genera and species in regions south of the Holarctic. In material collected by Vít Kubáò (Laos Expedition 1999), a hitherto undescribed species with conspicuously formed abdomen. It is described here as a new genus. Naticornus gen.nov. Type species: Naticornus luteum sp.nov. Description.
    [Show full text]
  • Ohara\Catalogues\World Genera\Tach
    WORLD GENERA OF THE TACHINIDAE (DIPTERA) AND THEIR REGIONAL OCCURRENCE by James E. O’Hara1 23 February 2005 Version 1.0 ________________________ 1 Invertebrate Biodiversity, Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario, Canada, K1A 0C6. E-mail: [email protected]. TABLE OF CONTENTS Click on a page number to go to the page indicated Foreword ............................................................................................................................... 2 Biogeographic summary ....................................................................................................... 3 Acknowledgements ............................................................................................................... 3 Table of genera and their regional occurrence ...................................................................... 4 References ........................................................................................................................... 66 Select a letter to go directly to corresponding genus in list of world genera 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 FOREWORD The following table is a listing of the tachinid genera of the world with their regional occurrence. It was compiled from the generic names and distributions given in the most recent regional catalogues, as listed here, and brought up-to-date using information from subsequently published papers. Regional catalogues Nearctic Region O’Hara & Wood (2004) Neotropical
    [Show full text]
  • Chironominae 8.1
    CHIRONOMINAE 8.1 SUBFAMILY CHIRONOMINAE 8 DIAGNOSIS: Antennae 4-8 segmented, rarely reduced. Labrum with S I simple, palmate or plumose; S II simple, apically fringed or plumose; S III simple; S IV normal or sometimes on pedicel. Labral lamellae usually well developed, but reduced or absent in some taxa. Mentum usually with 8-16 well sclerotized teeth; sometimes central teeth or entire mentum pale or poorly sclerotized; rarely teeth fewer than 8 or modified as seta-like projections. Ventromental plates well developed and usually striate, but striae reduced or vestigial in some taxa; beard absent. Prementum without dense brushes of setae. Body usually with anterior and posterior parapods and procerci well developed; setal fringe not present, but sometimes with bifurcate pectinate setae. Penultimate segment sometimes with 1-2 pairs of ventral tubules; antepenultimate segment sometimes with lateral tubules. Anal tubules usually present, reduced in brackish water and marine taxa. NOTESTES: Usually the most abundant subfamily (in terms of individuals and taxa) found on the Coastal Plain of the Southeast. Found in fresh, brackish and salt water (at least one truly marine genus). Most larvae build silken tubes in or on substrate; some mine in plants, dead wood or sediments; some are free- living; some build transportable cases. Many larvae feed by spinning silk catch-nets, allowing them to fill with detritus, etc., and then ingesting the net; some taxa are grazers; some are predacious. Larvae of several taxa (especially Chironomus) have haemoglobin that gives them a red color and the ability to live in low oxygen conditions. With only one exception (Skutzia), at the generic level the larvae of all described (as adults) southeastern Chironominae are known.
    [Show full text]
  • Diptera: Milichiidae), Attracted to Various Crushed Bugs (Hemiptera: Coreidae & Pentatomidae)
    16 Kondo et al., Milichiella lacteipennis attracted to crushed bugs REPORT OF MILICHIELLA LACTEIPENNIS LOEW (DIPTERA: MILICHIIDAE), ATTRACTED TO VARIOUS CRUSHED BUGS (HEMIPTERA: COREIDAE & PENTATOMIDAE) Takumasa Kondo Corporación Colombiana de Investigación Agropecuaria (CORPOICA), Centro de Investigación Palmira, Colombia; correo electrónico: [email protected] Irina Brake Natural History Museum, London, UK; correo electrónico: [email protected] Karol Imbachi López Universidad Nacional de Colombia, Sede Palmira, Colombia; correo electrónico: [email protected] Cheslavo A. Korytkowski University of Panama, Central American Entomology Graduate Program, Panama City, Panama; correo electrónico: [email protected] RESUMEN Diez especies en cuatro familias de hemípteros: Coreidae, Pentatomidae, Reduviidae y Rhyparochromidae fueron aplastadas con las manos para estudiar su atracción hacia Milichiella lacteipennis Loew (Diptera: Mi- lichiidae). Milichiella lacteipennis fue atraída solamente a chinches de Coreidae y Pentatomidae, y en general más fuertemente hacia las hembras que a los machos. Cuando eran atraídas, el tiempo de la llegada del primer milichiido a los chinches aplastados tuvo un rango entre 2 a 34 segundos dependiendo del sexo y de la especie de chinche. Solo las hembras adultas de M. lacteipennis fueron atraídas a los chinches. Palabras clave: experimento de atracción, Milichiella, Coreidae, Pentatomidae, Reduviidae, Rhyparochro- midae. SUMMARY Ten species in four hemipteran families: Coreidae, Pentatomidae, Reduviidae, and Rhyparochromidae were crushed by hand to test their attraction towards Milichiella lacteipennis Loew (Diptera: Milichiidae). Milichiella lacteipennis was attracted only to bugs of the families Coreidae and Pentatomidae, and was generally more strongly attracted to females than males. When attracted, the time of arrival of the first milichiid fly to the crushed bugs ranged from 2 to 34 seconds depending on the species and sex of the bug tested.
    [Show full text]
  • Revision of the Neotropical Neurigoninae
    NAGLIS: 267314 Studia dipterologica 10 (2003) Heft 1 ɀ ISSN 0945-3954 Revision of the Neotropical Neurigoninae (Diptera: Dolichopodidae) V: Neurigona RONDANI [Revision der neotropischen Neurigoninae (Diptera: Dolichopodidae) V: Neurigona RONDANI] by Stefan M. NAGLIS Zurich (Switzerland) Abstract The Neotropical species of the genus Neurigona RONDANI (Diptera: Dolichopodidae) are re- vised, comprising 39 species of which 32 are described as new. Descriptions, illustrations and keys to species and species-groups are given. The following species are described as new (spec. nov.): alajuela (Costa Rica), albitarsis (Costa Rica), aragua (Venezuela), argentifacies (Costa Rica, Brazil), brevitibia (Venezuela, Peru, Brazil), cantareira (Brazil), crinitarsis (Mexico), guanacasta (Costa Rica), hachaensis (Costa Rica), lamellata (Costa Rica, Panama, Honduras), latifacies (Costa Rica), limonensis (Costa Rica, Venezuela), longipalpa (Costa Rica), longitarsis (Costa Rica), maculosa (Tobago, Panama), magnipalpa (Costa Rica), mi- cra (Costa Rica), montebello (Mexico), nervosa (Costa Rica), obscurata (Mexico), pitilla (Costa Rica), plumitarsis (Costa Rica), pressitarsis (Venezuela), procera (Honduras), pseudobanksi (Brazil), purulha (Guatemala), sirena (Costa Rica, Panama, Venezuela, Guyana, Peru, Bra- zil), starki (Venezuela), subnervosa (Mexico, Guatemala), tatumbia (Mexico, Honduras), tenuicauda (Venezuela), yacambo (Venezuela). Neurigona banksi VAN DUZEE has been raised from synonymy. Neurigona brasiliensis (SCHINER) and Neurigona derelicta PARENT are
    [Show full text]
  • Checklist of the Family Chironomidae (Diptera) of Finland
    A peer-reviewed open-access journal ZooKeys 441: 63–90 (2014)Checklist of the family Chironomidae (Diptera) of Finland 63 doi: 10.3897/zookeys.441.7461 CHECKLIST www.zookeys.org Launched to accelerate biodiversity research Checklist of the family Chironomidae (Diptera) of Finland Lauri Paasivirta1 1 Ruuhikoskenkatu 17 B 5, FI-24240 Salo, Finland Corresponding author: Lauri Paasivirta ([email protected]) Academic editor: J. Kahanpää | Received 10 March 2014 | Accepted 26 August 2014 | Published 19 September 2014 http://zoobank.org/F3343ED1-AE2C-43B4-9BA1-029B5EC32763 Citation: Paasivirta L (2014) Checklist of the family Chironomidae (Diptera) of Finland. In: Kahanpää J, Salmela J (Eds) Checklist of the Diptera of Finland. ZooKeys 441: 63–90. doi: 10.3897/zookeys.441.7461 Abstract A checklist of the family Chironomidae (Diptera) recorded from Finland is presented. Keywords Finland, Chironomidae, species list, biodiversity, faunistics Introduction There are supposedly at least 15 000 species of chironomid midges in the world (Armitage et al. 1995, but see Pape et al. 2011) making it the largest family among the aquatic insects. The European chironomid fauna consists of 1262 species (Sæther and Spies 2013). In Finland, 780 species can be found, of which 37 are still undescribed (Paasivirta 2012). The species checklist written by B. Lindeberg on 23.10.1979 (Hackman 1980) included 409 chironomid species. Twenty of those species have been removed from the checklist due to various reasons. The total number of species increased in the 1980s to 570, mainly due to the identification work by me and J. Tuiskunen (Bergman and Jansson 1983, Tuiskunen and Lindeberg 1986).
    [Show full text]
  • Huchard Et Al., 2006 1.Pdf
    Acetylcholinesterase genes within the Diptera: takeover and loss in true flies Elise Huchard, Michel Martinez, Haoues Alout, Emmanuel Douzery, Georges Lutfalla, Arnaud Berthomieu, Claire Berticat, Michel Raymond, Mylene Weill To cite this version: Elise Huchard, Michel Martinez, Haoues Alout, Emmanuel Douzery, Georges Lutfalla, et al.. Acetyl- cholinesterase genes within the Diptera: takeover and loss in true flies. Proceedings of the Royal Society B: Biological Sciences, Royal Society, The, 2006, 273 (1601), pp.2595-2604. 10.1098/rspb.2006.3621. hal-01945529 HAL Id: hal-01945529 https://hal.archives-ouvertes.fr/hal-01945529 Submitted on 29 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Proc. R. Soc. B (2006) 273, 2595–2604 doi:10.1098/rspb.2006.3621 Published online 18 July 2006 Acetylcholinesterase genes within the Diptera: takeover and loss in true flies Elise Huchard1, Michel Martinez2, Haoues Alout1, Emmanuel J. P. Douzery1, Georges Lutfalla3, Arnaud Berthomieu1, Claire Berticat1, Michel Raymond1,* and Myle`ne Weill1 1Institut des Sciences
    [Show full text]
  • 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.
    [Show full text]
  • Nomenclatural Studies Toward a World List of Diptera Genus-Group Names
    Nomenclatural studies toward a world list of Diptera genus-group names. Part V Pierre-Justin-Marie Macquart Evenhuis, Neal L.; Pape, Thomas; Pont, Adrian C. DOI: 10.11646/zootaxa.4172.1.1 Publication date: 2016 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Evenhuis, N. L., Pape, T., & Pont, A. C. (2016). Nomenclatural studies toward a world list of Diptera genus- group names. Part V: Pierre-Justin-Marie Macquart. Magnolia Press. Zootaxa Vol. 4172 No. 1 https://doi.org/10.11646/zootaxa.4172.1.1 Download date: 02. Oct. 2021 Zootaxa 4172 (1): 001–211 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Monograph ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4172.1.1 http://zoobank.org/urn:lsid:zoobank.org:pub:22128906-32FA-4A80-85D6-10F114E81A7B ZOOTAXA 4172 Nomenclatural Studies Toward a World List of Diptera Genus-Group Names. Part V: Pierre-Justin-Marie Macquart NEAL L. EVENHUIS1, THOMAS PAPE2 & ADRIAN C. PONT3 1 J. Linsley Gressitt Center for Entomological Research, Bishop Museum, 1525 Bernice Street, Honolulu, Hawaii 96817-2704, USA. E-mail: [email protected] 2 Natural History Museum of Denmark, Universitetsparken 15, 2100 Copenhagen, Denmark. E-mail: [email protected] 3Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PW, UK. E-mail: [email protected] Magnolia Press Auckland, New Zealand Accepted by D. Whitmore: 15 Aug. 2016; published: 30 Sept. 2016 Licensed under a Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0 NEAL L.
    [Show full text]