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The Birds (Aves) of Oromia, Ethiopia – an Annotated Checklist
European Journal of Taxonomy 306: 1–69 ISSN 2118-9773 https://doi.org/10.5852/ejt.2017.306 www.europeanjournaloftaxonomy.eu 2017 · Gedeon K. et al. This work is licensed under a Creative Commons Attribution 3.0 License. Monograph urn:lsid:zoobank.org:pub:A32EAE51-9051-458A-81DD-8EA921901CDC The birds (Aves) of Oromia, Ethiopia – an annotated checklist Kai GEDEON 1,*, Chemere ZEWDIE 2 & Till TÖPFER 3 1 Saxon Ornithologists’ Society, P.O. Box 1129, 09331 Hohenstein-Ernstthal, Germany. 2 Oromia Forest and Wildlife Enterprise, P.O. Box 1075, Debre Zeit, Ethiopia. 3 Zoological Research Museum Alexander Koenig, Centre for Taxonomy and Evolutionary Research, Adenauerallee 160, 53113 Bonn, Germany. * Corresponding author: [email protected] 2 Email: [email protected] 3 Email: [email protected] 1 urn:lsid:zoobank.org:author:F46B3F50-41E2-4629-9951-778F69A5BBA2 2 urn:lsid:zoobank.org:author:F59FEDB3-627A-4D52-A6CB-4F26846C0FC5 3 urn:lsid:zoobank.org:author:A87BE9B4-8FC6-4E11-8DB4-BDBB3CFBBEAA Abstract. Oromia is the largest National Regional State of Ethiopia. Here we present the first comprehensive checklist of its birds. A total of 804 bird species has been recorded, 601 of them confirmed (443) or assumed (158) to be breeding birds. At least 561 are all-year residents (and 31 more potentially so), at least 73 are Afrotropical migrants and visitors (and 44 more potentially so), and 184 are Palaearctic migrants and visitors (and eight more potentially so). Three species are endemic to Oromia, 18 to Ethiopia and 43 to the Horn of Africa. 170 Oromia bird species are biome restricted: 57 to the Afrotropical Highlands biome, 95 to the Somali-Masai biome, and 18 to the Sudan-Guinea Savanna biome. -
(Charadriiformes), from the Early Eocene of Portugal
a new wader, recurvirostridae (charadriiformes), from the early eocene of Portugal c. J. o. HARRlSON * * British Museum (Natural History), Sub-Department of Orni thology. Tring. Hertfordshire HP 23 6AP. U. K. pp. 9-16 Ciencias da Tena (UNL) Lisboa N.o 7 1983 figs. 1-2 RESUMO Palavras-chave: Aves - Eocenico basal- Silveirinha - Portugal Descreve-se uma nova avoceta (Aves, Charadriiformes, Recurviros tridae) do Eocenico basal de Silveirinha, Baixo Mondego. Ap6s compa ra~oes corn outras formas actuais e f6sseis, e denorninada Fluviatilavis antunesi, novo gen. novo sp. Mots-cles: Aves - Eocene basal- Silveirinha - Portugal Un avocet nouveau (Aves, Charadriiformes, Recurvirostridae) de I'Eocene basal du gisement de Silveirinha (region du Bas Mondego, Portugal Central) est d6crit et compare avec d'autres formes actueIles et fossiles. Apres discussion de ses affinites, l'avocet de Silveirinha est rapporte a Fluviatilavis antunesi, n. gen. n. sp. ABSTRACf Key-words: Aves - Early Eocene - Silveirinha - Portugal A new wader (Aves, Charadriiformes, Recurvirostridae) 'from the Early Eocene site of Silveirinha, in Lower Mondego region, Central Portugal, is described. Comparisons have been made with other forms, both extant and fossil; its affInities are discussed. Silveirinha wader is ascribed to Fluviatilavis antunesi, n. gen. n. sp. INTRODUCTION the anterior intermuscular line about two-fifths of the distance along the shaft. The popliteal depression is Among the material collected by Professor Dr. Miguel roughly triangular and bordered by an elongated and well Telles Antunes at the Early Eocene site at Silveirinha, -defined medial ridge. At the proximal end of the bone Central Portugal (see ANTUNES and RUSSELL, 1981), the trochanteric ridge is more anteriorly flattened to give are three bird bones. -
The First Record of Common Ringed Plover (Charadrius Hiaticula) in British Columbia
The First Record of Common Ringed Plover (Charadrius hiaticula) in British Columbia. By Rick Toochin. Submitted: April 15, 2019. Introduction and Distribution The Common Ringed Plover (Charadrius hiaticula) is a widespread Old World shorebird species that is found breeding in the Arctic and subarctic regions from Greenland, Europe, east to Siberia (O’Brien et al. 2006). In North America, this species breeds on Baffin Island, eastern Ellesmere Island (Godfrey 1986). The Common Ringed Plover winters primarily from Western Europe, the Mediterranean Basin, throughout Africa, including Madagascar, and the Middle East (Hayman et al. 1986, O’Brien et al. 2006, Brazil 2009). There are three recognized subspecies of the Common Ringed Plover (Thies et al. 2018). Distinction between the subspecies is based on moult; with features changing clinally North to South, rather than East to West, making it impossible to draw a dividing line in Northwestern Europe (del Hoyo et al. 1996, Snow and Perrins 1998). The nominate subspecies of Common Ringed Plover is (C. h. hiaticula ) which breeds from southern Scandinavia to Great Britain, and northwestern France (Wiersma et al. 2019). This subspecies winters from Great Britain, south into Africa (del Hoyo et al. 1996, Snow and Perrins 1998). The second subspecies of the Common Ringed Plover is (C. h. tundrae) which is found breeding from northern Scandinavia, and northern Russia east to the Chukotskiy Peninsula, and is a casual breeder also in the northern Bering Sea region of Alaska on St Lawrence Island (Wiersma et al. 2019). This subspecies winters in the Caspian Sea region, and from Southwest Asia, south and east to South Africa (Wiersma et al. -
Iucn Red Data List Information on Species Listed On, and Covered by Cms Appendices
UNEP/CMS/ScC-SC4/Doc.8/Rev.1/Annex 1 ANNEX 1 IUCN RED DATA LIST INFORMATION ON SPECIES LISTED ON, AND COVERED BY CMS APPENDICES Content General Information ................................................................................................................................................................................................................................ 2 Species in Appendix I ............................................................................................................................................................................................................................... 3 Mammalia ............................................................................................................................................................................................................................................ 4 Aves ...................................................................................................................................................................................................................................................... 7 Reptilia ............................................................................................................................................................................................................................................... 12 Pisces ................................................................................................................................................................................................................................................. -
Species Assessment for Mountain Plover (Charadrius Montanus)
SPECIES ASSESSMENT FOR MOUNTAIN PLOVER (CHARADRIUS MONTANUS ) IN WYOMING prepared by 1 2 HAMILTON SMITH AND DOUGLAS A. KEINATH 1 Wyoming Natural Diversity Database, University of Wyoming, 1000 E. University Ave, Dept. 3381, Laramie, Wyoming 82071; 307-766-3023 2 Zoology Program Manager, Wyoming Natural Diversity Database, University of Wyoming, 1000 E. University Ave, Dept. 3381, Laramie, Wyoming 82071; 307-766-3013; [email protected] drawing by Summers Scholl prepared for United States Department of the Interior Bureau of Land Management Wyoming State Office Cheyenne, Wyoming November 2004 Smith and Keinath – Charadrius montanus November 2004 Table of Contents INTRODUCTION ................................................................................................................................. 3 NATURAL HISTORY ........................................................................................................................... 4 Morphological Description ...................................................................................................... 4 Taxonomy and Distribution ..................................................................................................... 5 Habitat Requirements............................................................................................................. 6 General ............................................................................................................................................6 Breeding ..........................................................................................................................................7 -
Best of the Baltic - Bird List - July 2019 Note: *Species Are Listed in Order of First Seeing Them ** H = Heard Only
Best of the Baltic - Bird List - July 2019 Note: *Species are listed in order of first seeing them ** H = Heard Only July 6th 7th 8th 9th 10th 11th 12th 13th 14th 15th 16th 17th Mute Swan Cygnus olor X X X X X X X X Whopper Swan Cygnus cygnus X X X X Greylag Goose Anser anser X X X X X Barnacle Goose Branta leucopsis X X X Tufted Duck Aythya fuligula X X X X Common Eider Somateria mollissima X X X X X X X X Common Goldeneye Bucephala clangula X X X X X X Red-breasted Merganser Mergus serrator X X X X X Great Cormorant Phalacrocorax carbo X X X X X X X X X X Grey Heron Ardea cinerea X X X X X X X X X Western Marsh Harrier Circus aeruginosus X X X X White-tailed Eagle Haliaeetus albicilla X X X X Eurasian Coot Fulica atra X X X X X X X X Eurasian Oystercatcher Haematopus ostralegus X X X X X X X Black-headed Gull Chroicocephalus ridibundus X X X X X X X X X X X X European Herring Gull Larus argentatus X X X X X X X X X X X X Lesser Black-backed Gull Larus fuscus X X X X X X X X X X X X Great Black-backed Gull Larus marinus X X X X X X X X X X X X Common/Mew Gull Larus canus X X X X X X X X X X X X Common Tern Sterna hirundo X X X X X X X X X X X X Arctic Tern Sterna paradisaea X X X X X X X Feral Pigeon ( Rock) Columba livia X X X X X X X X X X X X Common Wood Pigeon Columba palumbus X X X X X X X X X X X Eurasian Collared Dove Streptopelia decaocto X X X Common Swift Apus apus X X X X X X X X X X X X Barn Swallow Hirundo rustica X X X X X X X X X X X Common House Martin Delichon urbicum X X X X X X X X White Wagtail Motacilla alba X X -
Bird Monitoring at Zackenberg, Northeast Greenland, 2010, with Comparrison with 1996-20091,2
Bird Populations 11:42-51 © The Institute for Bird Populations 2012 BIRD MONITORING AT ZACKENBERG, NORTHEAST GREENLAND, 2010, WITH COMPARRISON WITH 1996-20091,2 JANNIK HANSEN3, LARS HOLST HANSEN AND NIELS MARTIN SCHMIDT Department of Bioscience Aarhus University P.O. Box 358 DK-4000 Roskilde, Denmark JEROEN RENEERKENS Animal Ecology Group Centre for Ecological and Evolutionary Studies University of Groningen PO Box 14 9750 AA Haren, The Netherlands Abstract. In 2010, bird populations continue to be monitored in a 15.8 km2 designated area at Zackenberg Research Station in central Northeast Greenland. Results are presented and compared with those from previous seasons (1995 – 2009). The breeding bird census resulted in densities generally comparable with previous years, but with relatively high densities of Sanderling (Calidris alba) and Dunlin (Calidris alpina). For all wader species, nesting was early compared to previous years, but with extremely low nest success. The number of Long-tailed Skua (Stercorarius longicaudus) territories was lower than average, and only one pair nested (unsuccessfully) in the census area, reflecting a season with very low lemming numbers. For Barnacle Geese (Branta leucopsis), the mean brood size was low early in the season, but later in the season numbers were close to average. Key words: Monitoring, Arctic, waders, geese, Lapland bunting, Long-tailed Skua, Rock Ptarmigan, Snow Bunting, climate. MONITOREO DE AVES EN ZACKENBERG, NORESTE DE GROENLANDIA, 2010, CON UNA COMPARACION CON 1996-2009 Resumen. En 2010, el monitoreo de poblaciones de aves continuó en un área de 15.8 km2 designada en la Estación de Investigación de Zackenberg, en el centro del noreste de Groenlandia. -
Erling Jirle Och Markus Lagerqvist, Tk, April 2019 1 VETENSKAPLIGT NAMN SVENSKT NAMN ENGELS
STATUS i Sverige VETENSKAPLIGT NAMN SVENSKT NAMN ENGELSKT NAMN Noter (Scientific name) (Swedish name) (English name) (Notes) Ordning STRUTHIONIFORMES STRUTSFÅGLAR Familj Struthionidae Strutsar Ostriches Struthio camelus struts Common Ostrich Ordning ANSERIFORMES ANDFÅGLAR Familj Anatidae Änder Ducks, Geese and Swans Dendrocygna bicolor brun visseland Fulvous Whistling Duck Dendrocygna javanica orientvisseland Lesser Whistling Duck M Branta bernicla prutgås Brant Goose R Branta ruficollis rödhalsad gås Red-breasted Goose B Branta canadensis kanadagås Canada Goose B Branta leucopsis vitkindad gås Barnacle Goose (E) Branta hutchinsii dvärgkanadagås Cackling Goose (D) R Anser indicus stripgås Bar-headed Goose (D) 14 Anser rossii dvärgsnögås Ross's Goose (E) R Anser caerulescens snögås Snow Goose B Anser anser grågås Greylag Goose B Anser fabalis sädgås Bean Goose M Anser brachyrhynchus spetsbergsgås Pink-footed Goose M Anser albifrons bläsgås Greater White-fronted Goose B Anser erythropus fjällgås Lesser White-fronted Goose (E) R Cygnus atratus svart svan Black Swan Intr. B Cygnus olor knölsvan Mute Swan M Cygnus columbianus mindre sångsvan Tundra Swan B Cygnus cygnus sångsvan Whooper Swan Plectropterus gambensis sporrgås Spur-winged Goose Sarkidiornis melanotos knöland Comb Duck R Alopochen aegyptiaca nilgås Egyptian Goose B Tadorna tadorna gravand Common Shelduck R Tadorna ferruginea rostand Ruddy Shelduck (E) 83 Aix sponsa brudand Wood Duck (E) b Aix galericulata mandarinand Mandarin Duck Intr. Nettapus coromandelianus bomullsdvärgand Cotton -
Wildlife Ecology Provincial Resources
MANITOBA ENVIROTHON WILDLIFE ECOLOGY PROVINCIAL RESOURCES !1 ACKNOWLEDGEMENTS We would like to thank: Olwyn Friesen (PhD Ecology) for compiling, writing, and editing this document. Subject Experts and Editors: Barbara Fuller (Project Editor, Chair of Test Writing and Education Committee) Lindsey Andronak (Soils, Research Technician, Agriculture and Agri-Food Canada) Jennifer Corvino (Wildlife Ecology, Senior Park Interpreter, Spruce Woods Provincial Park) Cary Hamel (Plant Ecology, Director of Conservation, Nature Conservancy Canada) Lee Hrenchuk (Aquatic Ecology, Biologist, IISD Experimental Lakes Area) Justin Reid (Integrated Watershed Management, Manager, La Salle Redboine Conservation District) Jacqueline Monteith (Climate Change in the North, Science Consultant, Frontier School Division) SPONSORS !2 Introduction to wildlife ...................................................................................7 Ecology ....................................................................................................................7 Habitat ...................................................................................................................................8 Carrying capacity.................................................................................................................... 9 Population dynamics ..............................................................................................................10 Basic groups of wildlife ................................................................................11 -
Conservation Biology of the Endangered St. Helena Plover Charadrius Sanctaehelenae
Conservation biology of the endangered St. Helena Plover Charadrius sanctaehelenae Volume 1 of 1 Fiona Ewing Burns A thesis submitted for the degree of Doctor of Philosophy University of Bath Department of Biology and Biochemistry June 2011 COPYRIGHT Attention is drawn to the fact that copyright of this thesis rests with its author. A copy of this thesis has been supplied on condition that anyone who consults it is understood to recognise that its copyright rests with the author and they must not copy it or use material from it except as permitted by law or with the consent of the author This thesis may be made available for consultation within the University Library and may be photocopied or lent to other libraries for the purposes of consultation. 1 Contents Acknowledgements...........................................................................................................3 Abstract .............................................................................................................................5 Introduction.......................................................................................................................6 Chapter 1: Leg flags versus colour rings: a comparison of marking methods using a small shorebird, the St Helena Plover.............................................................................20 Chapter 2: The impact of introduced predators on an island endemic, the St. Helena Plover Charadrius sanctaehelenae .................................................................................33 -
An Oriental Plover Charadrius Veredus from the [95A, B]
Correspondence 79 Correspondence An Oriental Plover Charadrius veredus from the [95A, B]. The habitat is mainly comprises fishery ponds, and Digha-Shankarpur Estuary, West Bengal: An addition open sunlit areas with sparse vegetation. The site was about 500 to the avifauna of mainland India m from the seacoast. The Oriental Plover Charadrius veredus is a widely distributed wader that breeds during April–July, in the dry steppes, arid grasslands, salt pans, and desert habitats of southern Siberia, Russia, Mongolia, and north-eastern China (Ozerskaya & Zabelin 2006; Stewart et al. 2007; Hayman et al. 2011) and migrates Both: Arajush Payra southwards along the South-east Asian coasts to spend the winter in Indonesia and north-western Australia (Branson & Minton 2006; Stewart et al. 2007). While birding on 26 October 2020 at the Digha-Shankarpur Estuary (21.65°N, 87.56°E; 1 m asl) in Purba Medinipur District, 95A, B. The Oriental Plover was spotted amidst fishery ponds. West Bengal, India, I spotted a single Oriental Plover foraging on the ground at the periphery of coastal fishery ponds, alongside a Pacific Golden PloverPluvialis fulva. I first photographed it [94A, Oriental Plover is considered a very rare passage migrant in B] at 1650 h on 08 November 2020, at the periphery of a fish South-east Asia (Robson 2011). There is only one record of this culture pond. It was regularly sighted and photographed from 09 species from India, from an unknown locality in the Andaman to 13 November 2020, and on 16 November 2020. Islands, of a specimen collected by Dr. -
Order CHARADRIIFORMES: Waders, Gulls and Terns Family
Text extracted from Gill B.J.; Bell, B.D.; Chambers, G.K.; Medway, D.G.; Palma, R.L.; Scofield, R.P.; Tennyson, A.J.D.; Worthy, T.H. 2010. Checklist of the birds of New Zealand, Norfolk and Macquarie Islands, and the Ross Dependency, Antarctica. 4th edition. Wellington, Te Papa Press and Ornithological Society of New Zealand. Pages 191 & 211-212. Order CHARADRIIFORMES: Waders, Gulls and Terns The family sequence of Christidis & Boles (1994), who adopted that of Sibley et al. (1988) and Sibley & Monroe (1990), is followed here. Family RECURVIROSTRIDAE Bonaparte: Stilts and Avocets Subfamily RECURVIROSTRINAE Bonaparte: Stilts and Avocets Recurvirostrinae Bonaparte, 1831: Saggio dist. Metodica Anim. Vert.: 59 – Type genus Recurvirostra Linnaeus, 1758. Genus Himantopus Brisson Himantopus Brisson, 1760: Ornithologie 1: 46, 5: 33 – Type species (by tautonymy) Charadrius himantopus Linnaeus = Himantopus himantopus (Linnaeus). Hypsibates Nitzsch, 1827: in Ersch & Gruber, Allgem. Ency. Wiss. Künste 16: 150 – Type species (by monotypy) Charadrius himantopus Linnaeus = Himantopus himantopus (Linnaeus). Himantopus himantopus (Linnaeus) Pied Stilt Charadrius Himantopus Linnaeus, 1758: Syst. Nat., 10th edition 1: 151 – southern Europe. Almost cosmopolitan, five subspecies recognised. Himantopus himantopus leucocephalus Gould Pied Stilt Himantopus leucocephalus Gould, 1837: Synop. Birds Australia 2: pl. 34 (fide McAllan 2004, Notornis 51: 127) – New South Wales, Australia. Himantopus albus Ellman, 1861: Zoologist 19: 7470 – New Zealand. Himantopus picatus Ellman, 1861: Zoologist 19: 7470 – New Zealand. Himantopus albicollis Buller, 1875: Trans. Proc. N.Z. Inst. 7: 224 – Orari, Canterbury. Junior primary homonym of Himantopus albicollis Vieillot, 1817. Himantopus seebohmi picata Ellman; Hartert 1891, Kat. Vogel. Mus. Senckenb. Natur. Gesell. Frankfurt Main: 220.