Variation in Ectosymbiont Assemblages Associated with Rock Pigeons (Columba Livia) from Coast to Coast in Canada
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(Phthiraptera: Ischnocera), with an Overview of the Geographical Distribution of Chewing Lice Parasitizing Chicken
European Journal of Taxonomy 685: 1–36 ISSN 2118-9773 https://doi.org/10.5852/ejt.2020.685 www.europeanjournaloftaxonomy.eu 2020 · Gustafsson D.R. & Zou F. This work is licensed under a Creative Commons Attribution License (CC BY 4.0). Research article urn:lsid:zoobank.org:pub:151B5FE7-614C-459C-8632-F8AC8E248F72 Gallancyra gen. nov. (Phthiraptera: Ischnocera), with an overview of the geographical distribution of chewing lice parasitizing chicken Daniel R. GUSTAFSSON 1,* & Fasheng ZOU 2 1 Institute of Applied Biological Resources, Xingang West Road 105, Haizhu District, Guangzhou, 510260, Guangdong, China. 2 Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Guangdong, China. * Corresponding author: [email protected] 2 Email: [email protected] 1 urn:lsid:zoobank.org:author:8D918E7D-07D5-49F4-A8D2-85682F00200C 2 urn:lsid:zoobank.org:author:A0E4F4A7-CF40-4524-AAAE-60D0AD845479 Abstract. The geographical range of the typically host-specific species of chewing lice (Phthiraptera) is often assumed to be similar to that of their hosts. We tested this assumption by reviewing the published records of twelve species of chewing lice parasitizing wild and domestic chicken, one of few bird species that occurs globally. We found that of the twelve species reviewed, eight appear to occur throughout the range of the host. This includes all the species considered to be native to wild chicken, except Oxylipeurus dentatus (Sugimoto, 1934). This species has only been reported from the native range of wild chicken in Southeast Asia and from parts of Central America and the Caribbean, where the host is introduced. -
Cystoidosoma Hermaphroditus Sp. N., the First Representative of the Quill
© Institute of Parasitology, Biology Centre CAS Folia Parasitologica 2015, 62: 037 doi: 10.14411/fp.2015.037 http://folia.paru.cas.cz Research Article Cystoidosoma hermaphroditus [ of the quill mite family Ascouracaridae (Acari: Astigmata: Fabio Akashi Hernandes1 and Barry M. OConnor2 1 Departamento de Zoologia, Universidade Estadual Paulista, Rio Claro, São Paulo, Brazil; 2 Department of Ecology and Evolutionary Biology, Museum of Zoology, University of Michigan, Ann Arbor, Michigan, USA Abstract: The mite family Ascouracaridae Gaud et Atyeo, 1976 contains large-sized mites (mostly > 1 mm) which live inside the quills of birds of several orders. To date, no representative of this family has been found associated with the order Strigiformes (owls). In this paper, a new species of this family, Cystoidosoma hermaphroditus sp. n., is described from the tropical screech owl, Megascops choliba (Vieillot) (Aves: Strigiformes) from Brazil. This species is unique in having an external spermaduct, a primary duct and a rudimentary bursa copulatrix[ to adults of the genus Cystoidosoma Gaud et Atyeo, 1976 of the world is presented. Keywords: feather mites, Megascops choliba, [ The family Ascouracaridae Gaud et Atyeo, 1976 (Acari: from Brazil (Valim et al. 2011): Ascouracarus chordeili Astigmata) contains large-sized mites (> 1 mm) that inhab- Mironov et Fain, 2003 from Chordeiles rupestris (Spix) it the quills of several bird orders (Gaud and Atyeo 1996, (Caprimulgiformes), Cystoidosoma psittacivorae Dabert !"##$%&[ et Ehrnsberger, 1992 from Aratinga aurea (Gmelin), and a subfamily of the Syringobiidae Trouessart, 1897 by Gaud Cystoidosoma aratingae Mironov et Fain, 2003 from Arat- and Atyeo (1976) and later was elevated to family by Gaud inga jandaya (Gmelin) (Psittaciformes). -
Insecta: Phthiraptera)
ANNALES HISTORICO-NATURALES MUSEI NATIONALIS HUNGARICI Volume 104 Budapest, 2012 pp. 5–109 A checklist of lice of Hungary (Insecta: Phthiraptera) Z. VAS1*, J. RÉKÁSI2 & L. RÓZSA3 1 Hungarian Natural History Museum, H-1088 Budapest, Baross u. 13, Hungary; Department of Biomathematics and Informatics, Faculty of Veterinary Science, Szent István University, H-1078 Budapest, István u. 2, Hungary. E-mail: [email protected] 2 Pannonhalma Benedictiner School, H-9090 Pannonhalma, Vár 2, Hungary. E-mail: [email protected] 3 MTA-ELTE-MTM Ecology Research Group, H-1117 Budapest, Pázmány P. sétány 1/C, Hungary. E-mail: [email protected] A checklist of louse species and subspecies collected from wild or domestic (exotic pets excluded) birds and mammals including humans in Hungary since 1945 is provided. The list is based on formerly published data and includes 279 louse species and subspecies. Their hosts represent 156 bird and 30 mammal species. Additionally, further 550 louse species (and subspecies) are also listed, whose occurrence is likely as judged from geographic and host distribution but have not been detected yet. This paper presents the most complete review of the Hungarian louse fauna. – Louse, host association, birds, mammals, ectoparasites. INTRODUCTION Hungary’s sucking louse (Phthiraptera: Anoplura) fauna was summa- rized by PIOTROWSKI (1970). The chewing louse (Phthiraptera: Amblycera, Ischnocera) fauna was evaluated in two checklists (RÉKÁSI 1993a, 1994) summarizing data for avian and mammalian hosts separately. Subsequently, more recent world checklists for sucking lice (DURDEN &MUSSER 1994) and for chewing lice (PRICE et al. 2003) critically reviewed the nomenclature, taxonomy and host-parasite relationships of this insect order as a whole. -
Türleri Chewing Lice (Phthiraptera)
Kafkas Univ Vet Fak Derg RESEARCH ARTICLE 17 (5): 787-794, 2011 DOI:10.9775/kvfd.2011.4469 Chewing lice (Phthiraptera) Found on Wild Birds in Turkey Bilal DİK * Elif ERDOĞDU YAMAÇ ** Uğur USLU * * Selçuk University, Veterinary Faculty, Department of Parasitology, Alaeddin Keykubat Kampusü, TR-42075 Konya - TURKEY ** Anadolu University, Faculty of Science, Department of Biology, TR-26470 Eskişehir - TURKEY Makale Kodu (Article Code): KVFD-2011-4469 Summary This study was performed to detect chewing lice on some birds investigated in Eskişehir and Konya provinces in Central Anatolian Region of Turkey between 2008 and 2010 years. For this aim, 31 bird specimens belonging to 23 bird species which were injured or died were examined for the louse infestation. Firstly, the feathers of each bird were inspected macroscopically, all observed louse specimens were collected and then the examined birds were treated with a synthetic pyrethroid spray (Biyo avispray-Biyoteknik®). The collected lice were placed into the tubes with 70% alcohol and mounted on slides with Canada balsam after being cleared in KOH 10%. Then the collected chewing lice were identified under the light microscobe. Eleven out of totally 31 (35.48%) birds were found to be infested with at least one chewing louse species. Eighteen lice species were found belonging to 16 genera on infested birds. Thirteen of 18 lice species; Actornithophilus piceus piceus (Denny, 1842); Anaticola phoenicopteri (Coincide, 1859); Anatoecus pygaspis (Nitzsch, 1866); Colpocephalum heterosoma Piaget, 1880; C. polonum Eichler and Zlotorzycka, 1971; Fulicoffula lurida (Nitzsch, 1818); Incidifrons fulicia (Linnaeus, 1758); Meromenopon meropis Clay ve Meinertzhagen, 1941; Meropoecus meropis (Denny, 1842); Pseudomenopon pilosum (Scopoli, 1763); Rallicola fulicia (Denny, 1842); Saemundssonia lari Fabricius, O, 1780), and Trinoton femoratum Piaget, 1889 have been recorded from Turkey for the first time. -
Three Feather Mites(Acari: Sarcoptiformes: Astigmata)
Journal of Species Research 8(2):215-224, 2019 Three feather mites (Acari: Sarcoptiformes: Astigmata) isolated from Tringa glareola in South Korea Yeong-Deok Han and Gi-Sik Min* Department of Biological Sciences, Inha University, Incheon 22212, Republic of Korea *Correspondent: [email protected] We describe three feather mites recovered from a wood sandpiper Tringa glareola that was stored in a -20°C freezer at the Chungnam Wild Animal Rescue Center. These feather mites are reported for the first time in South Korea: Avenzoaria totani (Canestrini, 1978), Ingrassia veligera Oudemans, 1904 and Mon tchadskiana glareolae Dabert and Ehrnsberger, 1999. In this study, we provide morphological diagnoses and illustrations. Additionally, we provide partial sequences of the mitochondrial cytochrome c oxidase subunit I (COI) gene as molecular characteristics of three species. Keywords: Avenzoaria totani, COI, feather mite, Ingrassia veligera, Montchadskiana glareolae, wood sandpiper, South Korea Ⓒ 2019 National Institute of Biological Resources DOI:10.12651/JSR.2019.8.2.215 INTRODUCTION is absent in males (Vasjukova and Mironov, 1991). The genus Montchadskiana is one of five genera that The wood sandpiper Tringa glareola (Linnaeus, 1758) belong to the subfamily Magimeliinae Gaud, 1972 and inhabits swamp and marshes (wet heathland, spruce or contains 17 species (Gaud and Atyeo, 1996; Dabert and birch forest) in the northern Eurasian continent (Pulliain- Ehrnsberger, 1999). This genus was found on flight feath- en and Saari, 1991; del Hoyo et al., -
Co-Extinct and Critically Co-Endangered Species of Parasitic Lice, and Conservation-Induced Extinction: Should Lice Be Reintroduced to Their Hosts?
Short Communication Co-extinct and critically co-endangered species of parasitic lice, and conservation-induced extinction: should lice be reintroduced to their hosts? L AJOS R ÓZSA and Z OLTÁN V AS Abstract The co-extinction of parasitic taxa and their host These problems highlight the need to develop reliable species is considered a common phenomenon in the current taxonomical knowledge about threatened and extinct global extinction crisis. However, information about the parasites. Although the co-extinction of host-specific conservation status of parasitic taxa is scarce. We present a dependent taxa (mutualists and parasites) and their hosts global list of co-extinct and critically co-endangered is known to be a feature of the ongoing wave of global parasitic lice (Phthiraptera), based on published data on extinctions (Stork & Lyal, 1993; Koh et al., 2004; Dunn et al., their host-specificity and their hosts’ conservation status 2009), the magnitude of this threat is difficult to assess. according to the IUCN Red List. We list six co-extinct Published lists of threatened animal parasites only cover and 40 (possibly 41) critically co-endangered species. ixodid ticks (Durden & Keirans, 1996; Mihalca et al., 2011), Additionally, we recognize 2–4 species that went extinct oestrid flies (Colwell et al., 2009), helminths of Brazilian as a result of conservation efforts to save their hosts. vertebrates (Muñiz-Pereira et al., 2009) and New Zealand Conservationists should consider preserving host-specific mites and lice (Buckley et al., 2012). Our aim here is to lice as part of their efforts to save species. provide a critical overview of the conservation status of parasitic lice. -
Terrestrial Arthropods)
Fall 2004 Vol. 23, No. 2 NEWSLETTER OF THE BIOLOGICAL SURVEY OF CANADA (TERRESTRIAL ARTHROPODS) Table of Contents General Information and Editorial Notes..................................... (inside front cover) News and Notes Forest arthropods project news .............................................................................51 Black flies of North America published...................................................................51 Agriculture and Agri-Food Canada entomology web products...............................51 Arctic symposium at ESC meeting.........................................................................51 Summary of the meeting of the Scientific Committee, April 2004 ..........................52 New postgraduate scholarship...............................................................................59 Key to parasitoids and predators of Pissodes........................................................59 Members of the Scientific Committee 2004 ...........................................................59 Project Update: Other Scientific Priorities...............................................................60 Opinion Page ..............................................................................................................61 The Quiz Page.............................................................................................................62 Bird-Associated Mites in Canada: How Many Are There?......................................63 Web Site Notes ...........................................................................................................71 -
Gonads and Gametogenesis in Astigmatic Mites
ASD565_proof ■ 7 May 2014 ■ 1/18 Arthropod Structure & Development xxx (2014) 1e18 55 Contents lists available at ScienceDirect 56 57 Arthropod Structure & Development 58 59 60 journal homepage: www.elsevier.com/locate/asd 61 62 63 64 65 1 Gonads and gametogenesis in astigmatic mites (Acariformes: 66 2 67 3 Astigmata) 68 4 69 * 5 Q1 Wojciech Witalinski 70 6 71 Department of Comparative Anatomy, Institute of Zoology, Jagiellonian University, Gronostajowa 9, 30-387 Kraków, Poland 7 72 8 73 9 article info abstract 74 10 75 11 76 Article history: Astigmatans are a large group of mites living in nearly every environment and exhibiting very diverse 12 Received 13 February 2014 reproductive strategies. In spite of an uniform anatomical organization of their reproductive systems, 77 13 Received in revised form gametogenesis in each sex is highly variable, leading to gamete formation showing many peculiar fea- 78 7 April 2014 14 tures and emphasizing the distinct position of Astigmata. This review summarizes the contemporary 79 Accepted 9 April 2014 15 knowledge on the structure of ovaries and testes in astigmatic mites, the peculiarities of oogenesis and 80 16 spermatogenesis, as well as provides new data on several species not studied previously. New questions 81 Keywords: 17 are discussed and approaches for future studies are proposed. 82 Ovarian nutritive cell Ó 18 Testicular central cell 2014 The Author. Published by Elsevier Ltd. This is an open access article under the CC BY license 83 19 Intercellular bridges (http://creativecommons.org/licenses/by/3.0/). 84 20 Ovary 85 Oogenesis 21 86 22 Vitellogenesis Testis 87 23 Spermatogenesis 88 24 Spermatozoa 89 25 Gonadal somatic cells 90 26 91 27 92 28 93 1. -
Infesting Rock Pigeons and Mourning Doves (Aves: Columbiformes: Columbidae) in Manitoba, with New Records for North America and Canada
208 Serendipity with chewing lice (Phthiraptera: Menoponidae, Philopteridae) infesting rock pigeons and mourning doves (Aves: Columbiformes: Columbidae) in Manitoba, with new records for North America and Canada Terry D. Galloway1 Department of Entomology, University of Manitoba, Winnipeg, Manitoba, Canada R3T 2N2 Ricardo L. Palma Museum of New Zealand Te Papa Tongarewa, P.O. Box 467, Wellington, New Zealand Abstract—An extensive survey of chewing lice from rock pigeon, Columba livia Gmelin, and mourning dove, Zenaida macroura (L.), carried out from 1994 to 2000 and from 2003 to 2006 in Manitoba, Canada, produced the following new records: Coloceras tovornikae Tendeiro for North America; Columbicola macrourae (Wilson), Hohorstiella lata (Piaget), H. paladinella Hill and Tuff, and Physconelloides zenaidurae (McGregor) for Canada; and Bonomiella columbae Emerson, Campanulotes compar (Burmeister), Columbicola baculoides (Paine), and C. columbae (L.) for Manitoba. We collected 25 418 lice of four species (C. compar, C. columbae, H. lata, and C. tovornikae) from 322 rock pigeons. The overall prevalence of infestation was 78.9%, 52.5%, and 23.3% for C. compar, C. columbae, and H. lata, respectively. Coloceras tovornikae was not discovered until 2003, after which its prevalence was 39.9% on 114 pigeons. We col- lected 1116 lice of five species (P. zenaidurae, C. baculoides, C. macrourae, H. paladinella, and B. columbae) from 117 mourning doves. Physconelloides zenaidurae was encountered most often (prevalence was 36.7%), while the prevalence of the other four species was 26.3%, 18.4%, 3.5%, and 2.6%, respectively. Galloway218 and Palma Résumé—Une étude approfondie de poux mâcheurs sur des pigeons bisets, Colomba livia Gme- lin, et des tourterelles tristes, Zenaida macroura (L.), effectuée de 1994 à 2000 et de 2003 à 2006 au Manitoba, Canada, a produit les nouvelles mentions suivantes : Coloceras tovornikae Tendeiro pour l’Amérique du Nord; Columbicola macrourae (Wilson), Hohorstiella lata (Piaget), H. -
Astigmata: Analgoidea: Avenzoariidae) from Saudi Arabia: a New Species and Two New Records
Zootaxa 3710 (1): 061–071 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3710.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:36BEB161-20B5-472C-9815-53C86AD647E1 Feather mites of the genus Zachvatkinia Dubinin, 1949 (Astigmata: Analgoidea: Avenzoariidae) from Saudi Arabia: A new species and two new records MOHAMED W. NEGM1,4,5, MOHAMED G. E.-D. NASSER2, FAHAD J. ALATAWI1, AZZAM M. AL AHMAD2 & MOHAMMED SHOBRAK3 1Acarology Laboratory, Department of Plant Protection, College of Food & Agriculture Sciences, King Saud University, Riyadh 11451, P.O. Box 2460, Saudi Arabia 2Medical & Veterinary Entomology Unit, Department of Plant Protection, College of Food & Agriculture Sciences, King Saud Univer- sity, Riyadh 11451, P.O. Box 2460, Saudi Arabia 3Department of Biology, College of Science, Taif University, Taif, P.O. Box 888, Saudi Arabia 4Permanent address: Department of Plant Protection, Faculty of Agriculture, Assiut University, Assiut 71526, Egypt. 5Corresponding author. E-mail: [email protected] Abstract Feather mites of the family Avenzoariidae (Acari: Astigmata: Analgoidea) are recorded for the first time in Saudi Arabia. A new avenzoariid species, Zachvatkinia (Zachvatkinia) repressae sp. n. (Avenzoariidae: Bonnetellinae), is described from the White-cheeked Tern, Sterna repressa Hartert, 1916 (Charadriiformes: Sternidae). The new species belongs to the sternae group and is closely related to Z. (Z.) chlidoniae Mironov, 1989a. Two more species, Z. (Z.) dromae Mironov, 1992 and Z. (Z.) sternae (Canestrini & Fanzago, 1876), were collected from the Crab Plover Dromas ardeola Paykull, 1805 (Charadriiformes: Dromadidae) and the Sooty Gull Ichthyaetus hemprichii (Bruch, 1853) (Charadriiformes: Laridae), re- spectively. -
Parasitic Helminths and Arthropods of Fulvous Whistling-Ducks (Dendrocygna Bicolor) in Southern Florida
J. Helminthol. Soc. Wash. 61(1), 1994, pp. 84-88 Parasitic Helminths and Arthropods of Fulvous Whistling-Ducks (Dendrocygna bicolor) in Southern Florida DONALD J. FORRESTER,' JOHN M. KINSELLA,' JAMES W. MERTiNS,2 ROGER D. PRICE,3 AND RICHARD E. TuRNBULL4 5 1 Department of Infectious Diseases, College of Veterinary Medicine, University of Florida, Gainesville, Florida 32610, 2 U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Veterinary Services, National Veterinary Services Laboratories, P.O. Box 844, Ames, Iowa 50010, 1 Department of Entomology, University of Minnesota, St. Paul, Minnesota 55108, and 4 Florida Game and Fresh Water Fish Commission, Okeechobee, Florida 34974 ABSTRACT: Thirty fulvous whistling-ducks (Dendrocygna bicolor) collected during 1984-1985 from the Ever- glades Agricultural Area of southern Florida were examined for parasites. Twenty-eight species were identified and included 8 trematodes, 6 cestodes, 1 nematode, 4 chewing lice, and 9 mites. All parasites except the 4 species of lice and 1 of the mites are new host records for fulvous whistling-ducks. None of the ducks were infected with blood parasites. Every duck was infected with at least 2 species of helminths (mean 4.2; range 2- 8 species). The most common helminths were the trematodes Echinostoma trivolvis and Typhlocoelum cucu- merinum and 2 undescribed cestodes of the genus Diorchis, which occurred in prevalences of 67, 63, 50, and 50%, respectively. Only 1 duck was free of parasitic arthropods; each of the other 29 ducks was infested with at least 3 species of arthropods (mean 5.3; range 3-9 species). The most common arthropods included an undescribed feather mite (Ingrassia sp.) and the chewing louse Holomenopon leucoxanthum, both of which occurred in 97% of the ducks. -
The Mallophaga of New England Birds James Edward Keirans Jr
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 1966 THE MALLOPHAGA OF NEW ENGLAND BIRDS JAMES EDWARD KEIRANS JR. Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation KEIRANS, JAMES EDWARD JR., "THE MALLOPHAGA OF NEW ENGLAND BIRDS" (1966). Doctoral Dissertations. 834. https://scholars.unh.edu/dissertation/834 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received 67—163 KEIRANS, Jr., James Edward, 1935— THE MALLOPHAGA OF NEW ENGLAND BIRDS. University of New Hampshire, Ph.D., 1966 E n tom ology University Microfilms, Inc., Ann Arbor, Michigan THE MALLOPHAGA OF NEW ENGLAND BIRDS BY JAMES E.° KEIRANS, -TK - A. B,, Boston University, i960 A. M., Boston University, 19^3 A THESIS Submitted to The University of New Hampshire In Partial Fulfillment of The Requirements for the Degree of Doctor of Philosophy Graduate School Department of Zoology June, 1966 This thesis has been examined and approved. May 12i 1966 Date ACKNOWLEDGEMENT I wish to express my thanks to Dr. James G. Conklin, Chairman, Department of Entomology and chairman of my doctoral committee, for his guidance during the course of these studies and for permission to use the facilities of the Entomology Department. My grateful thanks go to Dr. Robert L.