Revision of the Status of Bird Species Occurring Or Reported in Colombia
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Santos, Aleixo, D'horta, Portes.Indd
ISSN (impresso) 0103-5657 ISSN (on-line) 2178-7875 Revista Brasileira de Ornitologia Volume 19 Número 2 www.ararajuba.org.br/sbo/ararajuba/revbrasorn Junho 2011 Publicada pela Sociedade Brasileira de Ornitologia São Paulo - SP Revista Brasileira de Ornitologia, 19(2), 134-153 ARTIGO Junho de 2011 Avifauna of the Juruti Region, Pará, Brazil Marcos Pérsio Dantas Santos1, Alexandre Aleixo2, Fernando Mendonça d’Horta3 and Carlos Eduardo Bustamante Portes4 1. Universidade Federal do Pará. Instituto de Ciências Biológicas. Laboratório de Ecologia e Zoologia de Vertebrados. Rua Augusto Corrêa, 1, Guamá, CEP 66075‑110, Belém, PA, Brasil. E‑mail: [email protected] 2. Museu Paraense Emílio Goeldi. Coordenação de Zoologia. Caixa Postal 399, CEP 66040‑170, Belém, PA, Brasil. E‑mail: aleixo@museu‑goeldi.br 3. Universidade de São Paulo. Instituto de Biociências. Departamento de Biologia. Rua do Matão, 277, Cidade Universitária, CEP 05508‑090, São Paulo, SP, Brasil. E‑mail: [email protected] 4. Museu Paraense Emílio Goeldi. Pós‑Graduação em Zoologia. Caixa Postal 399, CEP 66040‑170, Belém, PA, Brasil. E‑mail: [email protected] Recebido em 02/03/2011. Aceito em 18/05/2011. RESUMO: Avifauna da região do Juruti, Pará, Brasil. A região que compreende o interflúvio Madeira‑Tapajós é certamente uma das regiões brasileiras de maior complexidade ambiental e um dos mais importantes centros de endemismos de aves da América do Sul, denominado centro de endemismo Madeira ou Rondônia. Entretanto, essa região vem sofrendo um crescente aumento nas pressões antrópicas, principalmente pelo desmatamento, o que implica uma forte preocupação sobre a conservação de toda a biota dessa região. -
Bird List Column A: 1 = 70-90% Chance Column B: 2 = 30-70% Chance Column C: 3 = 10-30% Chance
Colombia: Chocó Prospective Bird List Column A: 1 = 70-90% chance Column B: 2 = 30-70% chance Column C: 3 = 10-30% chance A B C Tawny-breasted Tinamou 2 Nothocercus julius Highland Tinamou 3 Nothocercus bonapartei Great Tinamou 2 Tinamus major Berlepsch's Tinamou 3 Crypturellus berlepschi Little Tinamou 1 Crypturellus soui Choco Tinamou 3 Crypturellus kerriae Horned Screamer 2 Anhima cornuta Black-bellied Whistling-Duck 1 Dendrocygna autumnalis Fulvous Whistling-Duck 1 Dendrocygna bicolor Comb Duck 3 Sarkidiornis melanotos Muscovy Duck 3 Cairina moschata Torrent Duck 3 Merganetta armata Blue-winged Teal 3 Spatula discors Cinnamon Teal 2 Spatula cyanoptera Masked Duck 3 Nomonyx dominicus Gray-headed Chachalaca 1 Ortalis cinereiceps Colombian Chachalaca 1 Ortalis columbiana Baudo Guan 2 Penelope ortoni Crested Guan 3 Penelope purpurascens Cauca Guan 2 Penelope perspicax Wattled Guan 2 Aburria aburri Sickle-winged Guan 1 Chamaepetes goudotii Great Curassow 3 Crax rubra Tawny-faced Quail 3 Rhynchortyx cinctus Crested Bobwhite 2 Colinus cristatus Rufous-fronted Wood-Quail 2 Odontophorus erythrops Chestnut Wood-Quail 1 Odontophorus hyperythrus Least Grebe 2 Tachybaptus dominicus Pied-billed Grebe 1 Podilymbus podiceps Magnificent Frigatebird 1 Fregata magnificens Brown Booby 2 Sula leucogaster ________________________________________________________________________________________________________ WINGS ● 1643 N. Alvernon Way Ste. 109 ● Tucson ● AZ ● 85712 ● www.wingsbirds.com (866) 547 9868 Toll free US + Canada ● Tel (520) 320-9868 ● Fax (520) -
SPLITS, LUMPS and SHUFFLES Splits, Lumps and Shuffles Alexander C
>> SPLITS, LUMPS AND SHUFFLES Splits, lumps and shuffles Alexander C. Lees This series focuses on recent taxonomic proposals—be they entirely new species, splits, lumps or reorganisations—that are likely to be of greatest interest to birders. This latest instalment includes a new Scytalopus tapaculo and a new subspecies of Three-striped Warbler, reviews of species limits in Grey-necked Wood Rails and Pearly Parakeets and comprehensive molecular studies of Buff-throated Woodcreepers, Sierra Finches, Red-crowned Ant Tanagers and Siskins. Get your lists out! Splits proposed for Grey- Pearly Parakeet is two species necked Wood Rails The three subspecies of Pearly Parakeet Pyrrhura lepida form a species complex with Crimson- The Grey-necked Wood Rail Aramides cajaneus bellied Parakeet P. perlata and replace each other is both the most widespread (occurring from geographically across a broad swathe of southern Mexico to Argentina) and the only polytypic Amazonia east of the Madeira river all the way member of its genus. Although all populations to the Atlantic Ocean. Understanding the nature are ‘diagnosable’ in having an entirely grey neck of this taxonomic variation is an important task, and contrasting chestnut chest, there is much as collectively their range sits astride much of variation in the colours of the nape, lower chest the Amazonian ‘Arc of Deforestation’ and the and mantle, differences amongst which have led to broadly-defined Brazilian endemic Pearly Parakeet the recognition of nine subspecies. Marcondes and is already considered to be globally Vulnerable. Silveira (2015) recently explored the taxonomy of Somenzari and Silveira (2015) recently investigated Grey-necked Wood Rails based on morphological the taxonomy of the three lepida subspecies (the and vocal characteristics using a sample of 800 nominate P. -
Breeding Biology of Yellow-Browed Antbird Hypocnemis Hypoxantha
Daniel M. Brooks et al. 156 Bull. B.O.C. 2016 136(3) Breeding biology of Yellow-browed Antbird Hypocnemis hypoxantha by Daniel M. Brooks, Pablo Aibar, Pam Bucur, Ron Rossi & Harold F. Greeney Received 17 February 2016 Summary.—We provide novel data concerning the nests, eggs and parental care of Yellow-browed Antbird Hypocnemis hypoxantha based on two nests in eastern Ecuador and Peruvian Amazonia, one of which was video-taped. Both adults participated in incubation, with earliest and latest feeding events at 06.11 h and 17.22 h, respectively. Feeding behaviour is described, with intervals of 1–114 minutes (mean = 38.3 minutes) and tettigoniid cicadas the primary prey. Nestlings frequently produced faecal sacs (interval range = 4–132 minutes, mean = 37.8 minutes) immediately following food delivery, and the sac was always carried from the nest by an adult. Two events involving a parent bird being chased from the nest are described, the first involving a male Fulvous Antshrike Frederickena fulva. Systematics are discussed in light of nest morphology and architecture. Yellow-browed Antbird Hypocnemis hypoxantha is a distinctive Amazonian thamnophilid that comprises two currently recognised subspecies: nominate hypoxantha in western Amazonian lowland and foothill forests from southern Colombia south to central Peru, and H. h. ochraceiventris in south-east Amazonian Brazil (Zimmer & Isler 2003). Generally found below 400 m, the nominate subspecies occasionally ranges as high as 900 m (Zimmer & Isler 2003, Ridgely & Tudor 2009). The species’ reproductive biology is almost completely unknown (Zimmer & Isler 2003). Willis (1988) provided a cursory description of a nest with nestlings from Colombia, but included few details of the nest and no description of the eggs or behaviour. -
Dacninae Species Tree, Part I
Dacninae I: Nemosiini, Conirostrini, & Diglossini Hooded Tanager, Nemosia pileata Cherry-throated Tanager, Nemosia rourei Nemosiini Blue-backed Tanager, Cyanicterus cyanicterus White-capped Tanager, Sericossypha albocristata Scarlet-throated Tanager, Sericossypha loricata Bicolored Conebill, Conirostrum bicolor Pearly-breasted Conebill, Conirostrum margaritae Chestnut-vented Conebill, Conirostrum speciosum Conirostrini White-eared Conebill, Conirostrum leucogenys Capped Conebill, Conirostrum albifrons Giant Conebill, Conirostrum binghami Blue-backed Conebill, Conirostrum sitticolor White-browed Conebill, Conirostrum ferrugineiventre Tamarugo Conebill, Conirostrum tamarugense Rufous-browed Conebill, Conirostrum rufum Cinereous Conebill, Conirostrum cinereum Stripe-tailed Yellow-Finch, Pseudochloris citrina Gray-hooded Sierra Finch, Phrygilus gayi Patagonian Sierra Finch, Phrygilus patagonicus Peruvian Sierra Finch, Phrygilus punensis Black-hooded Sierra Finch, Phrygilus atriceps Gough Finch, Rowettia goughensis White-bridled Finch, Melanodera melanodera Yellow-bridled Finch, Melanodera xanthogramma Inaccessible Island Finch, Nesospiza acunhae Nightingale Island Finch, Nesospiza questi Wilkins’s Finch, Nesospiza wilkinsi Saffron Finch, Sicalis flaveola Grassland Yellow-Finch, Sicalis luteola Orange-fronted Yellow-Finch, Sicalis columbiana Sulphur-throated Finch, Sicalis taczanowskii Bright-rumped Yellow-Finch, Sicalis uropigyalis Citron-headed Yellow-Finch, Sicalis luteocephala Patagonian Yellow-Finch, Sicalis lebruni Greenish Yellow-Finch, -
Provisional List of Birds of the Rio Tahuauyo Areas, Loreto, Peru
Provisional List of Birds of the Rio Tahuauyo areas, Loreto, Peru Compiled by Carol R. Foss, Ph.D. and Josias Tello Huanaquiri, Guide Status based on expeditions from Tahuayo Logde and Amazonia Research Center TINAMIFORMES: Tinamidae 1. Great Tinamou Tinamus major 2. White- throated Tinamou Tinamus guttatus 3. Cinereous Tinamou Crypturellus cinereus 4. Little Tinamou Crypturellus soui 5. Undulated Tinamou Crypturellus undulates 6. Variegated Tinamou Crypturellus variegatus 7. Bartlett’s Tinamou Crypturellus bartletti ANSERIFORMES: Anhimidae 8. Horned Screamer Anhima cornuta ANSERIFORMES: Anatidae 9. Muscovy Duck Cairina moschata 10. Blue-winged Teal Anas discors 11. Masked Duck Nomonyx dominicus GALLIFORMES: Cracidae 12. Spix’s Guan Penelope jacquacu 13. Blue-throated Piping-Guan Pipile cumanensis 14. Speckled Chachalaca Ortalis guttata 15. Wattled Curassow Crax globulosa 16. Razor-billed Curassow Mitu tuberosum GALLIFORMES: Odontophoridae 17. Marbled Wood-Quall Odontophorus gujanensis 18. Starred Wood-Quall Odontophorus stellatus PELECANIFORMES: Phalacrocoracidae 19. Neotropic Cormorant Phalacrocorax brasilianus PELECANIFORMES: Anhingidae 20. Anhinga Anhinga anhinga CICONIIFORMES: Ardeidae 21. Rufescent Tiger-Heron Tigrisoma lineatum 22. Agami Heron Agamia agami 23. Boat-billed Heron Cochlearius cochlearius 24. Zigzag Heron Zebrilus undulatus 25. Black-crowned Night-Heron Nycticorax nycticorax 26. Striated Heron Butorides striata 27. Cattle Egret Bubulcus ibis 28. Cocoi Heron Ardea cocoi 29. Great Egret Ardea alba 30. Cappet Heron Pilherodius pileatus 31. Snowy Egret Egretta thula 32. Little Blue Heron Egretta caerulea CICONIIFORMES: Threskiornithidae 33. Green Ibis Mesembrinibis cayennensis 34. Roseate Spoonbill Platalea ajaja CICONIIFORMES: Ciconiidae 35. Jabiru Jabiru mycteria 36. Wood Stork Mycteria Americana CICONIIFORMES: Cathartidae 37. Turkey Vulture Cathartes aura 38. Lesser Yellow-headed Vulture Cathartes burrovianus 39. -
A Classification of the Rallidae
A CLASSIFICATION OF THE RALLIDAE STARRY L. OLSON HE family Rallidae, containing over 150 living or recently extinct species T and having one of the widest distributions of any family of terrestrial vertebrates, has, in proportion to its size and interest, received less study than perhaps any other major group of birds. The only two attempts at a classifi- cation of all of the recent rallid genera are those of Sharpe (1894) and Peters (1934). Although each of these lists has some merit, neither is satisfactory in reflecting relationships between the genera and both often separate closely related groups. In the past, no attempt has been made to identify the more primitive members of the Rallidae or to illuminate evolutionary trends in the family. Lists almost invariably begin with the genus Rdus which is actually one of the most specialized genera of the family and does not represent an ancestral or primitive stock. One of the difficulties of rallid taxonomy arises from the relative homo- geneity of the family, rails for the most part being rather generalized birds with few groups having morphological modifications that clearly define them. As a consequence, particularly well-marked genera have been elevated to subfamily rank on the basis of characters that in more diverse families would not be considered as significant. Another weakness of former classifications of the family arose from what Mayr (194933) referred to as the “instability of the morphology of rails.” This “instability of morphology,” while seeming to belie what I have just said about homogeneity, refers only to the characteristics associated with flightlessness-a condition that appears with great regularity in island rails and which has evolved many times. -
The Conservation Ecology of the European Nightjar (Caprimulgus Europaeus) in a Complex Heathland-Plantation Landscape
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of East Anglia digital repository The conservation ecology of the European nightjar (Caprimulgus europaeus) in a complex heathland-plantation landscape. Katrina Sharps A thesis submitted for the degree of Doctor of Philosophy at the School of Environmental Sciences, University of East Anglia, Norwich, UK. May 2013 © This copy of the thesis has been supplied on condition that anyone who consults it is understood to recognise that its copyright rests with the author and that use of any information derived there from must be in accordance with current UK Copyright Law. In addition, any quotation or extract must include full attribution. Acknowledgements Firstly, I would like to thank my primary supervisor Paul Dolman for his constant advice, support and enthusiasm throughout this PhD. I am also grateful to the other members of my supervisory team: Ian Henderson of the British Trust for Ornithology (BTO) and Andrew Lovett of UEA, for their useful guidance. Special thanks also go to Neal Armour-Chelu of the Forestry Commission and Greg Conway of the BTO for practical advice for the fieldwork and their invaluable experience and knowledge of forest management and working with nightjars respectively. Next, I would like to thank the other members of my radio-tracking and moth trapping teams – Vivien Hartwell, Laura Wilkinson, Elwyn Sharps, Alastair Feather, Kirsten Miller and Isobel Winney. Their efforts were tireless and they showed dedication to the project throughout. Additional thanks to all radio-tracking and nest finding volunteers, including Forestry Commission, RSPB and Wildlife Trust staff. -
Pre-Concept for a Regional Project ______
ADAPTATION FUND BOARD SECRETARIAT TECHNICAL REVIEW OF PROJECT/PROGRAMME PROPOSAL PROJECT/PROGRAMME CATEGORY: Pre-Concept for a Regional Project _________________________________________________________________________________________________________ Countries/Region: Costa Rica and Dominican Republic/ LAC Project Title: Improving the adaptive capacity of coastal communities in Costa Rica and the Dominican Republic through ecosystem-based adaptation strategies Thematic Focal Area: Ecosystem Based Adaptation (EbA) Implementing Entity: Development Bank of Latin America (CAF) Executing Entities: Sistema Nacional de Áreas de Conservación (Costa Rica) and Ministerio de Medio Ambiente y Recursos Naturales (Dominican Republic) AF Project ID: LAC/RIE/EBA/2020/PPC/1 IE Project ID: <IE to fill out> Requested Financing From Adaptation Fund (US Dollars): 13,919,202 Reviewer and contact person: Alyssa Gomes, Martina Dorigo (AFSEC) Co-reviewer(s): Jason Spensley (GEFSEC) IE Contact Person: <IE to fill out> Technical The project “Improving the adaptive capacity of coastal communities in Costa Rica and the Dominican Republic Summary through ecosystem-based adaptation strategies” aims to improve local adaptive capacity to reduce the vulnerability to climate change of Cocos and Catalina islands and the production sectors that depend on their ecosystem services. This will be done through the four components below: Project/Programme Background and Context: Component 1: Reduction oF main anthropogenic pressures (USD 6,590,000). Component 2: Conservation oF coral reefs (USD 525,000). Component 3: Insurance tools for emergency action (USD 3,550,000). Component 4: Knowledge management (USD 710,000). Requested Financing overview: Project/Programme Execution Cost: USD 1,513,150 Total Project/Programme Cost: USD 12,888,150 Implementing Fee: USD 1,031,052 Financing Requested: USD 13,919,202 The proposal does not include a request For a project Formulation grant. -
Eagle-Eye Tours Guyana Tour Species List January 17-29, 2019
Guyana Tour Species List Tour Leader: Paul Prior Eagle-Eye Tours January 17-29, 2019 BIRD SPECIES Seen/ Common Name Scientific Name Heard TINAMOUS 1 Great Tinamou Tinamus major H 2 Cinereous Tinamou Crypturellus cinereus H 3 Little Tinamou Crypturellus soui H 4 Undulated Tinamou Crypturellus undulatus H 5 Red-legged Tinamou Crypturellus erythropus H 6 Variegated Tinamou Crypturellus variegatus H DUCKS, GEESE, AND WATERFOWL 7 White-faced Whistling-Duck Dendrocygna viduata S 8 Muscovy Duck Cairina moschata S 9 Masked Duck Nomonyx dominicus S GUANS, CHACHALACAS, AND CURASSOWS 10 Variable Chachalaca Ortalis motmot S 11 Marail Guan Penelope marail S 12 Spix's Guan Penelope jacquacu S 13 Black Curassow Crax alector S NEW WORLD QUAIL 14 Crested Bobwhite Colinus cristatus S FLAMINGOS 15 American Flamingo Phoenicopterus ruber S GREBES 16 Least Grebe Tachybaptus dominicus S 17 Pied-billed Grebe Podilymbus podiceps S STORKS 18 Maguari Stork Ciconia maguari S 19 Jabiru Jabiru mycteria S 20 Wood Stork Mycteria americana S FRIGATEBIRDS 21 Magnificent Frigatebird Fregata magnificens S CORMORANTS AND SHAGS 22 Neotropic Cormorant Phalacrocorax brasilianus S ANHINGAS 23 Anhinga Anhinga anhinga S PELICANS 24 Brown Pelican Pelecanus occidentalis S HERONS, EGRETS, AND BITTERNS Page1 of 15 Guyana Tour Species List Tour Leader: Paul Prior Eagle-Eye Tours January 17-29, 2019 BIRD SPECIES Seen/ Common Name Scientific Name Heard 25 Pinnated bittern Botaurus pinnatus S 26 Cocoi Heron Ardea cocoi S 27 Great Egret Ardea alba S 28 Snowy Egret Egretta thula S 29 Little -
Reproductive Biology and Nest-Site Selection of the Mato Grosso Antbird Cercomacra Melanaria in the Brazilian Pantanal
Revista Brasileira de Ornitologia, 22(3), 270-277 ARTICLE September 2014 Reproductive biology and nest-site selection of the Mato Grosso Antbird Cercomacra melanaria in the Brazilian Pantanal Bianca Bernardon1, 2, 3, Paula Fernanda Albonette de Nóbrega1 and João Batista de Pinho1 1 Laboratório de Ornitologia, Núcleo de Estudos Ecológicos do Pantanal, Instituto de Biociências, Universidade Federal de Mato Grosso – UFMT, Avenida Fernando Corrêa, s/nº, Coxipó, CEP 78060-900, Cuiabá, MT, Brazil 2 Current Address: Grupo de Pesquisa em Ecologia de Vertebrados Terrestres, Instituto de Desenvolvimento Sustentável Mamirauá – IDSM, Estrada do Bexiga, 2584, CEP 69553-225, Tefé, AM, Brazil 3 Corresponding author: [email protected] Received on 27 December 2013. Accepted on 26 June 2014. ABSTRACT: Economic activities, such as extensive cattle ranching, may seriously threaten the types of forest most important to the Mato Grosso Antbird Cercomacra melanaria, and information on reproductive biology is essential for defining sound conservation and management strategies for the species. Here, we report on the reproductive biology of this species in the Brazilian Pantanal, focusing on attributes such as incubation and nestling periods, as well as characteristics of parental care. The hypothesis that nest occurrence is associated with canopy opening was also tested. Average nest height was 0.98 m; mean nest construction and egg incubation periods were 12.2 and 14 days, respectively; average nestling period was 9.4 days. Both males and females participated in nest construction, egg incubation, and feeding of nestlings. The canopy was consistently more open away from the nests (18.74%) than at nest sites (10.10%; P < 0.0001), indicating that C. -
EASTERN ECUADOR RARITIES Custom Tour/ Nov-Dec 2020
Tropical Birding Tours - Trip Report EASTERN ECUADOR RARITIES Custom Tour/ Nov-Dec 2020 A Tropical Birding Tours CUSTOM BIRDING TOUR EASTERN ECUADOR RARITIES 26 Nov-6 Dec, 2020 Report and photos by ANDRES VASQUEZ N., the guide for this tour One of the most wanted birds of the World, the mighty queen of the jungle, Harpy Eagle (picture above at a nesting site). This is probably the easiest access to a nest of this awesome bird of prey in all of Latin America. It involves only a 5-minute car ride from the door of the hotel, 15 minute boat ride on the Napo River, and 2 easy walks of about 10 minutes each on flat but muddy terrain. The nesting pair has been recorded on this site a couple years ago by a local farmer who did not know much about the importance of the bird and therefore it remained “hidden” to the birding world until this year when the same farmer saw the couple again and this time mentioned it to the local guides who recently had been more active in terms of birding. The word spread out quickly and we were forced to tweak the itinerary that we already had for this custom tour and included a visit to the site. It was a tricky visit since just two days before our arrival, a group of scientists that visited the site recommended that no tourists should visit yet. However, since we were already there and it was only two visitors, we joined an already scheduled monitoring visit during which we stayed at the nest site for exactly 3.5 minutes, saw the bird, took a couple photos and left.