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Lista Roja De Las Aves Del Uruguay 1
Lista Roja de las Aves del Uruguay 1 Lista Roja de las Aves del Uruguay Una evaluación del estado de conservación de la avifauna nacional con base en los criterios de la Unión Internacional para la Conservación de la Naturaleza. Adrián B. Azpiroz, Laboratorio de Genética de la Conservación, Instituto de Investigaciones Biológicas Clemente Estable, Av. Italia 3318 (CP 11600), Montevideo ([email protected]). Matilde Alfaro, Asociación Averaves & Facultad de Ciencias, Universidad de la República, Iguá 4225 (CP 11400), Montevideo ([email protected]). Sebastián Jiménez, Proyecto Albatros y Petreles-Uruguay, Centro de Investigación y Conservación Marina (CICMAR), Avenida Giannattasio Km 30.5. (CP 15008) Canelones, Uruguay; Laboratorio de Recursos Pelágicos, Dirección Nacional de Recursos Acuáticos, Constituyente 1497 (CP 11200), Montevideo ([email protected]). Cita sugerida: Azpiroz, A.B., M. Alfaro y S. Jiménez. 2012. Lista Roja de las Aves del Uruguay. Una evaluación del estado de conservación de la avifauna nacional con base en los criterios de la Unión Internacional para la Conservación de la Naturaleza. Dirección Nacional de Medio Ambiente, Montevideo. Descargo de responsabilidad El contenido de esta publicación es responsabilidad de los autores y no refleja necesariamente las opiniones o políticas de la DINAMA ni de las organizaciones auspiciantes y no comprometen a estas instituciones. Las denominaciones empleadas y la forma en que aparecen los datos no implica de parte de DINAMA, ni de las organizaciones auspiciantes o de los autores, juicio alguno sobre la condición jurídica de países, territorios, ciudades, personas, organizaciones, zonas o de sus autoridades, ni sobre la delimitación de sus fronteras o límites. -
Disaggregation of Bird Families Listed on Cms Appendix Ii
Convention on the Conservation of Migratory Species of Wild Animals 2nd Meeting of the Sessional Committee of the CMS Scientific Council (ScC-SC2) Bonn, Germany, 10 – 14 July 2017 UNEP/CMS/ScC-SC2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II (Prepared by the Appointed Councillors for Birds) Summary: The first meeting of the Sessional Committee of the Scientific Council identified the adoption of a new standard reference for avian taxonomy as an opportunity to disaggregate the higher-level taxa listed on Appendix II and to identify those that are considered to be migratory species and that have an unfavourable conservation status. The current paper presents an initial analysis of the higher-level disaggregation using the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World Volumes 1 and 2 taxonomy, and identifies the challenges in completing the analysis to identify all of the migratory species and the corresponding Range States. The document has been prepared by the COP Appointed Scientific Councilors for Birds. This is a supplementary paper to COP document UNEP/CMS/COP12/Doc.25.3 on Taxonomy and Nomenclature UNEP/CMS/ScC-Sc2/Inf.3 DISAGGREGATION OF BIRD FAMILIES LISTED ON CMS APPENDIX II 1. Through Resolution 11.19, the Conference of Parties adopted as the standard reference for bird taxonomy and nomenclature for Non-Passerine species the Handbook of the Birds of the World/BirdLife International Illustrated Checklist of the Birds of the World, Volume 1: Non-Passerines, by Josep del Hoyo and Nigel J. Collar (2014); 2. -
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property
Appendix 1: Maps and Plans Appendix184 Map 1: Conservation Categories for the Nominated Property. Los Alerces National Park, Argentina 185 Map 2: Andean-North Patagonian Biosphere Reserve: Context for the Nominated Proprty. Los Alerces National Park, Argentina 186 Map 3: Vegetation of the Valdivian Ecoregion 187 Map 4: Vegetation Communities in Los Alerces National Park 188 Map 5: Strict Nature and Wildlife Reserve 189 Map 6: Usage Zoning, Los Alerces National Park 190 Map 7: Human Settlements and Infrastructure 191 Appendix 2: Species Lists Ap9n192 Appendix 2.1 List of Plant Species Recorded at PNLA 193 Appendix 2.2: List of Animal Species: Mammals 212 Appendix 2.3: List of Animal Species: Birds 214 Appendix 2.4: List of Animal Species: Reptiles 219 Appendix 2.5: List of Animal Species: Amphibians 220 Appendix 2.6: List of Animal Species: Fish 221 Appendix 2.7: List of Animal Species and Threat Status 222 Appendix 3: Law No. 19,292 Append228 Appendix 4: PNLA Management Plan Approval and Contents Appendi242 Appendix 5: Participative Process for Writing the Nomination Form Appendi252 Synthesis 252 Management Plan UpdateWorkshop 253 Annex A: Interview Guide 256 Annex B: Meetings and Interviews Held 257 Annex C: Self-Administered Survey 261 Annex D: ExternalWorkshop Participants 262 Annex E: Promotional Leaflet 264 Annex F: Interview Results Summary 267 Annex G: Survey Results Summary 272 Annex H: Esquel Declaration of Interest 274 Annex I: Trevelin Declaration of Interest 276 Annex J: Chubut Tourism Secretariat Declaration of Interest 278 -
Notes on Some Argentine Anatids
NOTESON SOME ARGENTINEANATIDS' MILTON W. WELLER ROM mid-August, 1964, until late July, 1965, I was engaged in field work F in Argentina studying waterfowl. Although special emphasis was placed on the Black-headed Duck (Heteronetta atricapilla) , 28 species of anatids were observed in various parts of Argentina. Because so little is known of these species, some general observations are summarized and discussed in the hope that it will point out gaps in our knowledge and encourage additional work on this interesting group. Field work was financed by Grant GB-1067 from the National Science Foundation. Studies of museum specimens in the United States were financed by a Chapman Grant of the American Museum of Natural History, and aided materially in appraising the significance of plumage sequences in Neotropical ducks. AQUATIC HABITATS Although the distribution of Argentine birds was considered by Dabbene (1910) and by Olrog (19591, little comment has been made on the distribution of water types and their influence on waterfowl distribution. Some helpful botanical comments are given by Cabrera (1953) for the Buenos Aires region and, Wetmores’ (1926) observations on both botany and ornithology are excellent. Although time did not permit detailed botanical work during this study, some obvious differences in life-form of marsh vegetation were recorded in the areas visited (Fig. 1) in relation to the species composi- tion of waterbirds. The most extensive zone of freshwater and semipermanent marshes is found in an area roughly bordered by the cities of Venado Tuerto (Santa Fe), Buenos Aires, General Lavalle, Mar de1 Plats and Azul (Buenos Aires). -
Bolivia: Endemic Macaws & More!
BOLIVIA: ENDEMIC MACAWS & MORE! PART II: FOOTHILLS, CLOUDFORESTS & THE ALTIPLANO SEPTEMBER 28–OCTOBER 8, 2018 Male Versicolored Barbet – Photo Andrew Whittaker LEADERS: ANDREW WHITTAKER & JULIAN VIDOZ LIST COMPILED BY: ANDREW WHITTAKER VICTOR EMANUEL NATURE TOURS, INC. 2525 WALLINGWOOD DRIVE, SUITE 1003 AUSTIN, TEXAS 78746 WWW.VENTBIRD.COM Bolivia continued to exceed expectations on Part 2 of our tour! Steadily climbing up into the mighty ceiling of South America that is the Andes, we enjoyed exploring many more new, different, and exciting unspoiled bird-rich habitats, including magical Yungas cloudforest stretching as far as the eye could see; dry and humid Puna; towering snow-capped Andean peaks; vast stretches of Altiplano with its magical brackish lakes filled with immense numbers of glimmering flamingoes, and one of my favorite spots, the magnificent and famous Lake Titicaca (with its own flightless grebe). An overdose of stunning Andean scenery combined with marvelous shows of flowering plants enhanced our explorations of a never-ending array of different and exciting microhabitats for so many special and interesting Andean birds. We were rewarded with a fabulous trip record total of 341 bird species! Combining our two exciting Bolivia tours (Parts 1 and 2) gave us an all-time VENT record, an incredible grand total of 656 different bird species and 15 mammals! A wondrous mirage of glimmering pink hues of all three species of flamingos on the picturesque Bolivian Altiplano – Photo Andrew Whittaker Stunning Andes of Bolivia near Soroto on a clear day of our 2016 trip – Photo Andrew Whittaker Victor Emanuel Nature Tours 2 Bolivia Part 2, 2018 We began this second part of our Bolivian bird bonanza in the bustling city of Cochabamba, spending a fantastic afternoon birding the city’s rich lakeside in lovely late afternoon sun. -
Patagonia Wildlife Safari Paul Prior BIRD SPECIES - Total 177 Seen/ No
BIRD CHECKLIST Leaders: Steve Ogle Eagle-Eye Tours 2018 Patagonia Wildlife Safari Paul Prior BIRD SPECIES - Total 177 Seen/ No. Common Name Latin Name Heard RHEIFORMES: Rheidae 1 Lesser Rhea Rhea pennata s TINAMIFORMES: Tinamidae 2 Elegant Crested-Tinamou Eudromia elegans s ANSERIFORMES: Anhimidae 3 Southern Screamer Chauna torquata s ANSERIFORMES: Anatidae 4 White-faced Whistling-Duck Dendrocygna viduata s 5 Fulvous Whistling-Duck Dendrocygna bicolor s 6 Black-necked Swan Cygnus melancoryphus s 7 Coscoroba Swan Coscoroba coscoroba s 8 Upland Goose Chloephaga picta s 9 Kelp Goose Chloephaga hybrida s 10 Flying Steamer-Duck Tachyeres patachonicus s 11 Flightless Steamer-Duck Tachyeres pteneres s 12 White-headed Steamer-Duck Tachyeres leucocephalus s 13 Crested Duck Lophonetta specularioides s 14 Spectacled Duck Speculanas specularis s 15 Brazilian Teal Amazonetta brasiliensis s 16 Torrent Duck Merganetta armata s 17 Chiloe Wigeon Anas sibilatrix s 18 Cinnamon Teal Anas cyanoptera s 19 Red Shoveler Anas platalea s 20 Yellow-billed Pintail Anas georgica s 21 Silver Teal Anas versicolor s 22 Yellow-billed Teal Anas flavirostris s 23 Rosy-billed Pochard Netta peposaca s 24 Black-headed Duck Heteronetta atricapilla s 25 Lake Duck Oxyura vittata s PODICIPEDIFORMES: Podicipedidae 26 White-tufted Grebe Rollandia rolland s 27 Great Grebe Podiceps major s 28 Silvery Grebe Podiceps occipitalis s PHOENICOPTERIFORMES: Phoenicopteridae 29 Chilean Flamingo Phoenicopterus chilensis s SPHENISCIFORMES: Spheniscidae 30 King Penguin Aptenodytes patagonicus s 31 Gentoo Penguin Pygoscelis papua s 32 Magellanic Penguin Spheniscus magellanicus s PROCELLARIIFORMES: Diomedeidae 33 Black-browed Albatross Thalassarche melanophris s Page 1 of 6 BIRD CHECKLIST Leaders: Steve Ogle Eagle-Eye Tours 2018 Patagonia Wildlife Safari Paul Prior BIRD SPECIES - Total 177 Seen/ No. -
Handbook of Waterfowl Behavior: Tribe Anatini (Surface-Feeding Ducks)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Handbook of Waterfowl Behavior, by Paul Johnsgard Papers in the Biological Sciences January 1965 Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks) Paul A. Johnsgard University of Nebraska-Lincoln, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/bioscihandwaterfowl Part of the Ornithology Commons Johnsgard, Paul A., "Handbook of Waterfowl Behavior: Tribe Anatini (Surface-feeding Ducks)" (1965). Handbook of Waterfowl Behavior, by Paul Johnsgard. 16. https://digitalcommons.unl.edu/bioscihandwaterfowl/16 This Article is brought to you for free and open access by the Papers in the Biological Sciences at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Handbook of Waterfowl Behavior, by Paul Johnsgard by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Subfamily Anatinae 125 Aix. During extreme excitement the male will often roll his head on his back, or even bathe. I have not observed Preening-behind-the- wing, but W. von de Wall (pers. comm.) has observed a male per- form it toward a female. Finally, Wing-flapping appears to be used as a display by males, and it is especially conspicuous because each sequence of it is ended by a rapid stretching of both wings over the back in a posture that makes visible the white axillary feathers, which contrast sharply with the black underwing surface. Copulatory behavior. Precopulatory behavior consists of the male swimming up to the female, his neck stretched and his crest de- pressed, and making occasional Bill-dipping movements. He then suddenly begins to perform more vigorous Head-dipping movements, and the female, if receptive, performs similar Bill-dipping or Head- dipping movements. -
P0083-P0090.Pdf
HABITAT SELECTION BY WATERFOWL OF ARGENTINE ISLA GRANDE MILTON W. WELLER Isla Grande is the main island of the archipelago at the tip of South Amer- ica known as Tierra de1 Fuego. Current knowledge of the birds of Isla Grande has been ably summarized by Humphrey et al. (1970). As part of a study of austral waterfowl, I spent the period from 10 January to 9 Feb- ruary 1972 at three locations on Isla Grande. I recorded 84 of 108 bird spe- cies recorded by Humphrey et al. (op. cit.), including 15 of the 17 known species of waterfowl. The purpose of this paper is to discuss habitat selec- tion of Isla Grande waterfowl. Observations are also presented on their pa- rental care, brood sizes and reproductive behavior. Data on stage of the reproductive cycle were gathered by age classification of broods according to the system described by Taber (1969:330) : Class I = downy young; II = partly down and partly contour feathers; III = full juvenal body plum- age but not yet flying. Observations spanned two major study areas, the southern mountainous beech forest along the Beagle Channel and the open steppe zone of northern Isla Grande. Nineteen days were spent at Estancia Harberton on the Beagle Channel, four days from Ushuaia west to Lapataia, and nine days at Estancia Viamonte and the region west and north of Rio Grande (Fig. 1). STUDY AREAS Estancia Harberton is along the Beagle Channel in an area of shoreline highly dis- sected with estuaries, bays and offshore islands. The terrain is rolling at sea level, rising in a series of hills to mountains of nearly 915 m. -
(Phthiraptera: Amblycera and Ischnocera) on Birds of Peru
Arxius de Miscel·lània Zoològica, 19 (2021): 7–52 ISSN:Minaya 1698– et0476 al. Checklist of chewing lice (Phthiraptera: Amblycera and Ischnocera) on birds of Peru D. Minaya, F. Príncipe, J. Iannacone Minaya, D., Príncipe, F., Iannacone, J., 2021. Checklist of chewing lice (Phthiraptera: Am- blycera and Ischnocera) on the birds of Peru. Arxius de Miscel·lània Zoològica, 19: 7–52, Doi: https://doi.org/10.32800/amz.2021.19.0007 Abstract Checklist of chewing lice (Phthiraptera: Amblycera and Ischnocera) on birds of Peru. Peru is one of the countries with the highest diversity of birds worldwide, having about 1,876 species in its territory. However, studies focused on chewing lice (Phthiraptera) have been carried out on only a minority of bird species. The available data are distributed in 87 publications in the national and international literature. In this checklist we summarize all the records to date of chewing lice on wild and domestic birds in Peru. Among the 301 species of birds studied, 266 species of chewing lice were recorded. The localities with the highest records were the Departments of Cusco, Junín, Lima and Madre de Dios. No records of birds pa- rasitized by these lice have been found in seven departments of Peru. Studies related to lice have only been reported in 16 % of bird species in the country, indicating that research concerning chewing lice has not yet been performed for the the majority of birds in Peru. Data published through GBIF (Doi: 10.15470/u1jtiu) Key words: Avifauna, Ectoparasites, Lice, Parasitology, Phthiraptera Resumen Lista de verificación de piojos masticadores (Phthiraptera: Amblycera e Ischnocera) de las aves de Perú. -
Host List of Avian Brood Parasites - 1 - Anatidae
HOST LIST OF AVIAN BROOD PARASITES - 1 - ANATIDAE Peter E. Lowther, Field Museum version 19 Oct 2008 (illustrations added 08 Jun 2012; new material added 29 Apr 2013, 18 Jul 2017) Heteronetta Heteronetta Salvadori 1865, Atti. Societa Italiana di Scienze Naturale e Museo Civico di Storia Naturale, 8, p. 374. Black-headed Duck, Heteronetta atricapilla (Merrem) 1841, Allgemeine Encyclopadie der Wissenschaften und Kunste in alphabetischer Folge von genannten Schriftstellern bearbeitet und hrsg. von J. S. Ersch und J. G. Gruber, sect. 1, 35, p. 26. General life history information given by Weller (1968, Lyon and Eadie 2013; see also Lowther 2010). Host list from Weller (1968), Höhn (1975), Lyon and Eadie 2013, Cabrera et al. 2017; see also Rees and Hillgarth (1984). Livzey (1986) presents waterfowl phylogeny showing Black-headed Duck to be sister- group to stiff-tails. Species known to have reared this brood parasite indicated by “%”. In captivity, reported hosts have included Rosy-billed Pochard Netta peposaca (Powell 1979, Rees and Hillgarth 1984), Red Shoveler Anas platalea (Todd 1979 1), and Common Moorhen Gallinula chloropus and Silver Teal Anas versicolor (Powell 1979 2. Rees and Hillgarth 1984). The Maguari Stork Ciconia maguari had been listed originally as a host based on supposed parasitic eggs which were later identified as being those of Rosy-billed Pochard Netta peposaca (see Weller 1968); subsequent records returns this species to this list of hosts (Cabrera et al. 2017). PODICIPEDIDAE Great Grebe, Podiceps major ARDEIDAE Black-crowned -
BIRDS of BOLIVIA UPDATED SPECIES LIST (Version 03 June 2020) Compiled By: Sebastian K
BIRDS OF BOLIVIA UPDATED SPECIES LIST (Version 03 June 2020) https://birdsofbolivia.org/ Compiled by: Sebastian K. Herzog, Scientific Director, Asociación Armonía ([email protected]) Status codes: R = residents known/expected to breed in Bolivia (includes partial migrants); (e) = endemic; NB = migrants not known or expected to breed in Bolivia; V = vagrants; H = hypothetical (observations not supported by tangible evidence); EX = extinct/extirpated; IN = introduced SACC = South American Classification Committee (http://www.museum.lsu.edu/~Remsen/SACCBaseline.htm) Background shading = Scientific and English names that have changed since Birds of Bolivia (2016, 2019) publication and thus differ from names used in the field guide BoB Synonyms, alternative common names, taxonomic ORDER / FAMILY # Status Scientific name SACC English name SACC plate # comments, and other notes RHEIFORMES RHEIDAE 1 R 5 Rhea americana Greater Rhea 2 R 5 Rhea pennata Lesser Rhea Rhea tarapacensis , Puna Rhea (BirdLife International) TINAMIFORMES TINAMIDAE 3 R 1 Nothocercus nigrocapillus Hooded Tinamou 4 R 1 Tinamus tao Gray Tinamou 5 H, R 1 Tinamus osgoodi Black Tinamou 6 R 1 Tinamus major Great Tinamou 7 R 1 Tinamus guttatus White-throated Tinamou 8 R 1 Crypturellus cinereus Cinereous Tinamou 9 R 2 Crypturellus soui Little Tinamou 10 R 2 Crypturellus obsoletus Brown Tinamou 11 R 1 Crypturellus undulatus Undulated Tinamou 12 R 2 Crypturellus strigulosus Brazilian Tinamou 13 R 1 Crypturellus atrocapillus Black-capped Tinamou 14 R 2 Crypturellus variegatus -
Falkland Islands Species List
Falkland Islands Species List Day Common Name Scientific Name x 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 1 BIRDS* 2 DUCKS, GEESE, & WATERFOWL Anseriformes - Anatidae 3 Black-necked Swan Cygnus melancoryphus 4 Coscoroba Swan Coscoroba coscoroba 5 Upland Goose Chloephaga picta 6 Kelp Goose Chloephaga hybrida 7 Ruddy-headed Goose Chloephaga rubidiceps 8 Flying Steamer-Duck Tachyeres patachonicus 9 Falkland Steamer-Duck Tachyeres brachypterus 10 Crested Duck Lophonetta specularioides 11 Chiloe Wigeon Anas sibilatrix 12 Mallard Anas platyrhynchos 13 Cinnamon Teal Anas cyanoptera 14 Yellow-billed Pintail Anas georgica 15 Silver Teal Anas versicolor 16 Yellow-billed Teal Anas flavirostris 17 GREBES Podicipediformes - Podicipedidae 18 White-tufted Grebe Rollandia rolland 19 Silvery Grebe Podiceps occipitalis 20 PENGUINS Sphenisciformes - Spheniscidae 21 King Penguin Aptenodytes patagonicus 22 Gentoo Penguin Pygoscelis papua Cheesemans' Ecology Safaris Species List Updated: April 2017 Page 1 of 11 Day Common Name Scientific Name x 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 23 Magellanic Penguin Spheniscus magellanicus 24 Macaroni Penguin Eudyptes chrysolophus 25 Southern Rockhopper Penguin Eudyptes chrysocome chrysocome 26 ALBATROSSES Procellariiformes - Diomedeidae 27 Gray-headed Albatross Thalassarche chrysostoma 28 Black-browed Albatross Thalassarche melanophris 29 Royal Albatross (Southern) Diomedea epomophora epomophora 30 Royal Albatross (Northern) Diomedea epomophora sanfordi 31 Wandering Albatross (Snowy) Diomedea exulans exulans 32 Wandering