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Diptera: Brachycera: Calyptratae) Inferred from Mitochondrial Genomes
University of Wollongong Research Online Faculty of Science, Medicine and Health - Papers: part A Faculty of Science, Medicine and Health 1-1-2015 The phylogeny and evolutionary timescale of muscoidea (diptera: brachycera: calyptratae) inferred from mitochondrial genomes Shuangmei Ding China Agricultural University Xuankun Li China Agricultural University Ning Wang China Agricultural University Stephen L. Cameron Queensland University of Technology Meng Mao University of Wollongong, [email protected] See next page for additional authors Follow this and additional works at: https://ro.uow.edu.au/smhpapers Part of the Medicine and Health Sciences Commons, and the Social and Behavioral Sciences Commons Recommended Citation Ding, Shuangmei; Li, Xuankun; Wang, Ning; Cameron, Stephen L.; Mao, Meng; Wang, Yuyu; Xi, Yuqiang; and Yang, Ding, "The phylogeny and evolutionary timescale of muscoidea (diptera: brachycera: calyptratae) inferred from mitochondrial genomes" (2015). Faculty of Science, Medicine and Health - Papers: part A. 3178. https://ro.uow.edu.au/smhpapers/3178 Research Online is the open access institutional repository for the University of Wollongong. For further information contact the UOW Library: [email protected] The phylogeny and evolutionary timescale of muscoidea (diptera: brachycera: calyptratae) inferred from mitochondrial genomes Abstract Muscoidea is a significant dipteran clade that includes house flies (Family Muscidae), latrine flies (F. Fannidae), dung flies (F. Scathophagidae) and root maggot flies (F. Anthomyiidae). It is comprised of approximately 7000 described species. The monophyly of the Muscoidea and the precise relationships of muscoids to the closest superfamily the Oestroidea (blow flies, flesh flies etc)e ar both unresolved. Until now mitochondrial (mt) genomes were available for only two of the four muscoid families precluding a thorough test of phylogenetic relationships using this data source. -
Fanniidae, Anthomyiidae, Muscidae) Described by P
Muscoidea (Fanniidae, Anthomyiidae, Muscidae) described by P. J. M. Macquart (Insecta, Diptera) Adrian C. PONT Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PW (United Kingdom) and Department of Entomology, The Natural History Museum, Cromwell Road, London SW7 5BD (United Kingdom) [email protected] Pont A. C. 2012. – Muscoidea (Fanniidae, Anthomyiidae, Muscidae) described by P. J. M. Macquart (Insecta, Diptera). Zoosystema 34 (1): 39-111. DOI : http://dx.doi.org/10.5252/z2012n1a3 ABSTRACT This paper deals with the 185 new species-group taxa that P. J. M. Macquart described in the dipteran families Fanniidae, Anthomyiidae and Muscidae, together with a further 5 species-group taxa that belong to other families, 9 replacement names that he proposed, and 1 nomen nudum. Notes are provided on the Diptera collections on which Macquart worked. In the Fanniidae, there are 8 species (and 1 replacement name), in Anthomyiidae, 33 species (and 4 replacement names), and in Muscidae, 144 species (and 4 replacement names). 85 lectotypes are newly designated in order to fix the identity of the names. The following new synonyms are proposed: in Anthomyiidae: Chortophila angusta Macquart, 1835 = Botanophila striolata (Fallén, 1824); Pegomyia basilaris Macquart, 1835 = Pegomya solennis (Meigen, 1826); Anthomyia brunnipennis Macquart, 1835, and Anthomyia fuscipennis Macquart, 1835 = Pegoplata aestiva (Meigen, 1826); Hylemyia caesia Macquart, 1835 = Anthomyia liturata (Robineau-Desvoidy, 1830); Chortophila caesia Macquart, -
The Evolution of Myiasis in Blowflies (Calliphoridae)
International Journal for Parasitology 33 (2003) 1105–1113 www.parasitology-online.com The evolution of myiasis in blowflies (Calliphoridae) Jamie R. Stevens* School of Biological Sciences, University of Exeter, Prince of Wales Road, Exeter EX4 4PS, UK Received 31 March 2003; received in revised form 8 May 2003; accepted 23 May 2003 Abstract Blowflies (Calliphoridae) are characterised by the ability of their larvae to develop in animal flesh. Where the host is a living vertebrate, such parasitism by dipterous larvae is known as myiasis. However, the evolutionary origins of the myiasis habit in the Calliphoridae, a family which includes the blowflies and screwworm flies, remain unclear. Species associated with an ectoparasitic lifestyle can be divided generally into three groups based on their larval feeding habits: saprophagy, facultative ectoparasitism, and obligate parasitism, and it has been proposed that this functional division may reflect the progressive evolution of parasitism in the Calliphoridae. In order to evaluate this hypothesis, phylogenetic analysis of 32 blowfly species displaying a range of forms of ectoparasitism from key subfamilies, i.e. Calliphorinae, Luciliinae, Chrysomyinae, Auchmeromyiinae and Polleniinae, was undertaken using likelihood and parsimony methods. Phylogenies were constructed from the nuclear 28S large subunit ribosomal RNA gene (28S rRNA), sequenced from each of the 32 calliphorid species, together with suitable outgroup taxa, and mitochondrial cytochrome oxidase subunit I and II (COI þ II) sequences, derived primarily from published data. Phylogenies derived from each of the two markers (28S rRNA, COI þ II) were largely (though not completely) congruent, as determined by incongruence-length difference and Kishino-Hasegawa tests. -
Lancs & Ches Muscidae & Fanniidae
The Diptera of Lancashire and Cheshire: Muscoidea, Part I by Phil Brighton 32, Wadeson Way, Croft, Warrington WA3 7JS [email protected] Version 1.0 21 December 2020 Summary This report provides a new regional checklist for the Diptera families Muscidae and Fannidae. Together with the families Anthomyiidae and Scathophagidae these constitute the superfamily Muscoidea. Overall statistics on recording activity are given by decade and hectad. Checklists are presented for each of the three Watsonian vice-counties 58, 59, and 60 detailing for each species the number of occurrences and the year of earliest and most recent record. A combined checklist showing distribution by the three vice-counties is also included, covering a total of 241 species, amounting to 68% of the current British checklist. Biodiversity metrics have been used to compare the pre-1970 and post-1970 data both in terms of the overall number of species and significant declines or increases in individual species. The Appendix reviews the national and regional conservation status of species is also discussed. Introduction manageable group for this latest regional review. Fonseca (1968) still provides the main This report is the fifth in a series of reviews of the identification resource for the British Fanniidae, diptera records for Lancashire and Cheshire. but for the Muscidae most species are covered by Previous reviews have covered craneflies and the keys and species descriptions in Gregor et al winter gnats (Brighton, 2017a), soldierflies and (2002). There have been many taxonomic changes allies (Brighton, 2017b), the family Sepsidae in the Muscidae which have rendered many of the (Brighton, 2017c) and most recently that part of names used by Fonseca obsolete, and in some the superfamily Empidoidea formerly regarded as cases erroneous. -
Molecular Phylogenetic Analysis of Nycteribiid and Streblid Bat Flies (Diptera: Brachycera, Calyptratae): Implications for Host
Molecular Phylogenetics and Evolution 38 (2006) 155–170 www.elsevier.com/locate/ympev Molecular phylogenetic analysis of nycteribiid and streblid bat Xies (Diptera: Brachycera, Calyptratae): Implications for host associations and phylogeographic origins Katharina Dittmar a,¤, Megan L. Porter b, Susan Murray c, Michael F. Whiting a a Department of Integrative Biology, Brigham Young University, 401 WIDB, Provo, UT 84602, USA b Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, USA c Department of Biology, Boston University, Boston, MA, USA Received 1 April 2005; revised 25 May 2005; accepted 6 June 2005 Available online 8 August 2005 Abstract Bat Xies are a small but diverse group of highly specialized ectoparasitic, obligatory bloodsucking Diptera. For the Wrst time, the phylogenetic relationships of 26 species and Wve subfamilies were investigated using four genes (18S rDNA, 16S rDNA, COII, and cytB) under three optimality criteria (maximum parsimony (MP), maximum likelihood (ML), and Bayesian inference). Tree topol- ogy tests of previous hypotheses were conducted under likelihood (Shimodaira–Hasegawa test). Major Wndings include the non- monophyly of the Streblidae and the recovery of an Old World- and a New World-Clade of bat Xies. These data ambiguously resolve basal relationships between Hippoboscidae, Glossinidae, and bat Xies. Recovered phylogenies resulted in either monophyly (Bayes- ian approach) or paraphyly (MP/ML topologies) of the bat Xies, thus obscuring the potential number of possible associations with bats throughout the history of this group. Dispersal-vicariance analysis suggested the Neotropical region as the possible ancestral distribution area of the New World Streblidae and the Oriental region for the Old World bat Xies. -
Adaptations of Insects at Cloudbridge Nature Reserve, Costa Rica
Adaptations of Insects at Cloudbridge Nature Reserve, Costa Rica Aiden Vey Cloudbridge Nature Reserve July 2007 Introduction Costa Rica’s location between North and South America, its neotropical climate and variety of elevations and habitats makes it one of the biodiversity hotspots of the world. Despite being only 51,100km² in size, it contains about 5% (505,000) of the world’s species. Of these, 35,000 insect species have been recorded and estimates stand at around 300,000. The more well known insects include the 8,000 species of moth and 1,250 butterflies - almost 10% of the world total, and 500 more than in the USA! Other abundant insects of Costa Rica include ants, beetles, wasps and bees, grasshoppers and katydids. The following article presents a select few aspects of the insect life found at Cloudbridge, a nature reserve in the Talamanca mountain range. Relationships Insects play many important roles in Costa Rica, including pollination of the bountiful flora and as a food supply for many other organisms. The adult Owl butterfly (Caligo atreus, shown at right) feeds on many Heliconiaceae and Musaceae (banana) species, in particular on the rotting fruit. They are pollinators of these plants, but also use the leaves to lay eggs on. When hatched, the larvae remain on the plant and eat the leaves. Being highly gregarious, they can cause significant damage, and are considered as pests (especially in banana plantations). However, there are a number of insects that parasitise the Caligo larvae, including the common Winthemia fly (left) and Trichogramma and Ichneumon wasps, which act as biological control agents. -
Diptera: Calliphoridae)1
Pacific Insects 13 (1) : 141-204 15 June 1971 THE TRIBE CALLIPHORINI FROM AUSTRALIAN AND ORIENTAL REGIONS II. CALLIPHORA-GROUP (Diptera: Calliphoridae)1 By Hiromu Kurahashi Abstract: The Australian and Oriental Calliphora-group consists of the following 5 genera: Xenocalliphora Malloch (6 spp.), Aldrichina Townsend (1 sp.), T Heer atopy ga Rohdendorf (1 sp.), Eucalliphora Townsend (1 sp.) and Calliphora Rob.-Desvoidy (37 spp.). The genus Calliphora Rob.-Desvoidy has a number of members with a greater diversity of form and coloration than do those known from any other faunal region, and it is subdivided into the 5 subgenera: Neocalliphora Brauer & Bergenstamm, Cal liphora s. str., Paracalliphora Townsend, Papuocalliphora n. subgen, and Australocalli- phora n. subgen, in the present paper. The following forms are described as new: Calliphora pseudovomitoria, Paracalliphora papuensis, P. kermadeca, P. norfolka, P. augur neocaledonensis, P. espiritusanta, P. porphyrina, P. gressitti, P. rufipes kermadecensis, P. rufipes tasmanensis, P. rufipes tahitiensis, Australocalliphora onesioidea and A. tasmaniae, This second study in the series on Australian and Oriental Calliphorini presents a revision of the Calliphora-group based on a much greater amount of material than the early authors had. Most of the specimens examined were available in the Department of Entomology, Bernice P. Bishop Museum, Honolulu. I have raised the number of species to 46 which belong to 5 genera: Xenocalliphora Malloch, Aldrichina Townsend, Triceratopyga Rohdendorf, Eucalliphora Townsend and Calliphora Rob.-Desvoidy. The former 4 are either monobasic or with few species in contrast with the 38 species of the last genus. They have several plesiomorphous characters, i.e., dichoptic condition of eyes in <^, in spite of a more or less high degree of specialization with respect to some features such as hypopygium. -
Definition of Diptera Cyclorrhapha Or Muscomorpha
vv ISSN: 2640-7795 DOI: https://dx.doi.org/10.17352/ojbs LIFE SCIENCES GROUP Received: 04 January, 2020 Short Communication Accepted: 12 March, 2020 Published: 13 March, 2020 *Corresponding author: Dr. Carlos Henrique Marchiori, Defi nition of Diptera Biological Sciences, Parasitology, Federal Institute Goiano, Goiânia, Brazil, E-mail: Cyclorrhapha or Muscomorpha Keywords: Flies; Myiasis; Synanthropic; Symbovines; Parasitism; Brazil Carlos Henrique Marchiori* https://www.peertechz.com Biological Sciences, Parasitology, Federal Institute Goiano, Goiânia, Brazil Abstract Some species of dipterous included in the infraorder Muscomorpha are of fundamental medical and veterinary importance, since they can produce myiasis and act towards transmission of pathogens to humans and animals. These dipterans are potential mechanical vectors for etiological agents such as viruses, bacteria, protozoan cysts and helminth eggs. This study aimed to make a defi nition of Diptera Cyclorrhapha or Muscomorpha, as well as their technical characteristics, interactions and classifi cation. Musca domestica L. (Diptera: Muscidae) is a specie of great sanitary interest because of its synanthropic characteristics, abundance in urban areas, capacity to develop in several sorts of substrates and high reproductive. Technical features Brachycera – Classification The 60,000 described species of Cyclorrhapha (Muscomorpha) (Figures 1-3) are characterized by an unusual Diptera (Order) diversity in larval life-history traits, which range from saprophagy over phytophagy to parasitism and predation. Act գ բ in the transmission of pathogens to humans and animals [1- Brachycera Nematocera (Sub-order) 4]. These diptera are potential mechanical vectors for etiologic agents, such as viruses, bacteria, protozoan cysts and helminth բ eggs [2]. բ The Cyclorrhapha is composed of those fl ies where the adult Muscomorpha or Cyclorrhapha ( Infra-order) escapes from the pupal case through a circular opening in the anterior end. -
Test Key to British Blowflies (Calliphoridae) And
Draft key to British Calliphoridae and Rhinophoridae Steven Falk 2016 BRITISH BLOWFLIES (CALLIPHORIDAE) AND WOODLOUSE FLIES (RHINOPHORIDAE) DRAFT KEY March 2016 Steven Falk Feedback to [email protected] 1 Draft key to British Calliphoridae and Rhinophoridae Steven Falk 2016 PREFACE This informal publication attempts to update the resources currently available for identifying the families Calliphoridae and Rhinophoridae. Prior to this, British dipterists have struggled because unless you have a copy of the Fauna Ent. Scand. volume for blowflies (Rognes, 1991), you will have been largely reliant on Van Emden's 1954 RES Handbook, which does not include all the British species (notably the common Pollenia pediculata), has very outdated nomenclature, and very outdated classification - with several calliphorids and tachinids placed within the Rhinophoridae and Eurychaeta palpalis placed in the Sarcophagidae. As well as updating keys, I have also taken the opportunity to produce new species accounts which summarise what I know of each species and act as an invitation and challenge to others to update, correct or clarify what I have written. As a result of my recent experience of producing an attractive and fairly user-friendly new guide to British bees, I have tried to replicate that approach here, incorporating lots of photos and clear, conveniently positioned diagrams. Presentation of identification literature can have a big impact on the popularity of an insect group and the accuracy of the records that result. Calliphorids and rhinophorids are fascinating flies, sometimes of considerable economic and medicinal value and deserve to be well recorded. What is more, many gaps still remain in our knowledge. -
Quality Control for Expanded Tsetse Production, Sterilization and Field Application
Quality Control for Control Quality Expanded Tsetse Production, Tsetse Expanded Sterilization and Field Application Field and Sterilization IAEA-TECDOC-1683 spine 7,4 mm IAEA-TECDOC-1683 n QUALITY CONTROL FOR EXPANDED TSETSE PRODUCTION, STERILIZatioN AND FIELD APPLicatioN 130110–9 VIENNA ISSN 1011–4289 ISBN 978–92–0– INTERNATIONAL ATOMIC AGENCY ENERGY ATOMIC INTERNATIONAL Quality Control for Expanded Tsetse Production, Sterilization and Field Application The following States are Members of the International Atomic Energy Agency: AFGHANISTAN GHANA NIGERIA ALBANIA GREECE NORWAY ALGERIA GUATEMALA OMAN ANGOLA HAITI PAKISTAN ARGENTINA HOLY SEE PALAU ARMENIA HONDURAS PANAMA AUSTRALIA HUNGARY PAPUA NEW GUINEA AUSTRIA ICELAND PARAGUAY AZERBAIJAN INDIA PERU BAHRAIN INDONESIA PHILIPPINES BANGLADESH IRAN, ISLAMIC REPUBLIC OF POLAND BELARUS IRAQ PORTUGAL IRELAND BELGIUM QATAR ISRAEL BELIZE REPUBLIC OF MOLDOVA BENIN ITALY ROMANIA BOLIVIA JAMAICA RUSSIAN FEDERATION BOSNIA AND HERZEGOVINA JAPAN SAUDI ARABIA BOTSWANA JORDAN SENEGAL BRAZIL KAZAKHSTAN SERBIA BULGARIA KENYA SEYCHELLES BURKINA FASO KOREA, REPUBLIC OF SIERRA LEONE BURUNDI KUWAIT SINGAPORE CAMBODIA KYRGYZSTAN CAMEROON LAO PEOPLES DEMOCRATIC SLOVAKIA CANADA REPUBLIC SLOVENIA CENTRAL AFRICAN LATVIA SOUTH AFRICA REPUBLIC LEBANON SPAIN CHAD LESOTHO SRI LANKA CHILE LIBERIA SUDAN CHINA LIBYA SWEDEN COLOMBIA LIECHTENSTEIN SWITZERLAND CONGO LITHUANIA SYRIAN ARAB REPUBLIC COSTA RICA LUXEMBOURG TAJIKISTAN CÔTE DIVOIRE MADAGASCAR THAILAND CROATIA MALAWI THE FORMER YUGOSLAV CUBA MALAYSIA REPUBLIC OF MACEDONIA -
Flies of Illinois
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New Species of Afrotropical Muscidae (Diptera: Muscoidea)
Zootaxa 3852 (3): 301–320 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2014 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3852.3.1 http://zoobank.org/urn:lsid:zoobank.org:pub:13B15A57-576A-4617-9D8A-7F27D970315A New species of Afrotropical Muscidae (Diptera: Muscoidea) MÁRCIA COURI1,3 & ADRIAN C. PONT2 1Museu Nacional, Quinta da Boa Vista, São Cristóvão, Rio de Janeiro, 20.940–040, RJ, Brazil, and Research Fellow, CNPq, Brazil. E-mail: [email protected] 2Oxford University Museum of Natural History, Parks Road, Oxford OX1 3PW, United Kingdom. E-mail: [email protected] 3Corresponding author. E-mail: [email protected] Abstract The study of recently collected Afrotropical Muscidae (Diptera) from Burundi, Democratic Republic of the Congo, Kenya and South Africa has revealed ten new species which are described herein: Coenosia duomaculata sp. nov., C. nigromac- ulata sp. nov., C. fragilis sp. nov., Helina harrisorum sp. nov., H. ferfriniorum sp. nov., Hydrotaea tantula sp. nov., Lim- nophora diminuta sp. nov., L. antennalis sp. nov., Spilogona brunnea sp. nov. and S. bella sp. nov. Coenosia, Helina and Limnophora are speciose muscid genera, found throughout the Afrotropical Region, while Hydrotaea and Spilogona have a more restricted geographic distribution and include some 20 species each. Key words: Afrotropical Region, Burundi, Democratic Republic of the Congo, Kenya, South Africa, diversity, taxonomy, new species Introduction The family Muscidae remains very poorly known in most areas of the Afrotropical Region. The family was last catalogued in this Region by Pont (1980), who listed 870 species in 59 genera.