Avian Monitoring Program
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The Birds of Reserva Ecológica Guapiaçu (REGUA)
Cotinga 33 The birds of Reserva Ecológica Guapiaçu (REGUA), Rio de Janeiro, Brazil Leonardo Pimentel and Fábio Olmos Received 30 September 2009; final revision accepted 15 December 2010 Cotinga 33 (2011): OL 8–24 published online 16 March 2011 É apresentada uma lista da avifauna da Reserva Ecológica de Guapiaçu (REGUA), uma reserva privada de 6.500 ha localizada no município de Cachoeiras de Macacu, vizinha ao Parque Estadual dos Três Picos, Estação Ecológica do Paraíso e Parque Nacional da Serra dos Órgãos, parte de um dos maiores conjuntos protegidos do Estado do Rio de Janeiro. Foram registradas um total de 450 espécies de aves, das quais 63 consideradas de interesse para conservação, como Leucopternis lacernulatus, Harpyhaliaetus coronatus, Triclaria malachitacea, Myrmotherula minor, Dacnis nigripes, Sporophila frontalis e S. falcirostris. A reserva também está desenvolvendo um projeto de reintrodução dos localmente extintos Crax blumembachii e Aburria jacutinga, e de reforço das populações locais de Tinamus solitarius. The Atlantic Forest of eastern Brazil and Some information has been published on neighbouring Argentina and Paraguay is among the birds of lower (90–500 m) elevations in the the most imperilled biomes in the world. At region10,13, but few areas have been subject to least 188 bird species are endemic to it, and 70 long-term surveys. Here we present the cumulative globally threatened birds occur there, most of them list of a privately protected area, Reserva Ecológica endemics4,8. The Atlantic Forest is not homogeneous Guapiaçu (REGUA), which includes both low-lying and both latitudinal and longitudinal gradients parts of the Serra dos Órgãos massif and nearby account for diverse associations of discrete habitats higher ground, now mostly incorporated within and associated bird communities. -
Long-Term Changes in the Bird Community of Palenque, Chiapas, in Response to Rainforest Loss
Biodivers Conserv (2010) 19:21–36 DOI 10.1007/s10531-009-9698-z ORIGINAL PAPER Long-term changes in the bird community of Palenque, Chiapas, in response to rainforest loss Michael A. Patten Æ He´ctor Go´mez de Silva Æ Brenda D. Smith-Patten Received: 18 March 2008 / Accepted: 22 July 2009 / Published online: 6 August 2009 Ó Springer Science+Business Media B.V. 2009 Abstract With increased human populations and subsequent pressure to develop or farm land, the rate of fragmentation of tropical rainforests has accelerated in the past several decades. How native organisms respond to such fragmentation has been the subject of intense study in temperate ecosystems and at several tropical sites in Central and South America, but there has been little study of this phenomenon in Mexico, the country bridging the Neotropics and temperate North America. A reason for this neglect is an apparent lack of long-term data; however, such data can be obtained from ‘‘non-tradi- tional’’ sources, such as birders and tour leaders. We make innovative use of such data, combining them with more traditional data (e.g., museum specimens) to create a record of occurrence for Palenque, Mexico, from 1900 to 2009, including a near-continuous pres- ence–absence record since 1970. We analyzed these data using logistic regression and, importantly, recent statistical advances expressly for sighting records. As recently as the 1960s Palenque’s forest was contiguous with that of Selva Lacandona to the east, but the protected area surrounding the famous ruins is now a forested island. As a result, various species formerly known from the site have disappeared, including species both large (Crax rubra, Penelope purpurascens, and Ara macao) and small (Notharchus hyperrhynchos, Malacoptila panamensis, Microrhopias quixensis, and Pachyramphus cinnamomeus). -
CAT Vertebradosgt CDC CECON USAC 2019
Catálogo de Autoridades Taxonómicas de vertebrados de Guatemala CDC-CECON-USAC 2019 Centro de Datos para la Conservación (CDC) Centro de Estudios Conservacionistas (Cecon) Facultad de Ciencias Químicas y Farmacia Universidad de San Carlos de Guatemala Este documento fue elaborado por el Centro de Datos para la Conservación (CDC) del Centro de Estudios Conservacionistas (Cecon) de la Facultad de Ciencias Químicas y Farmacia de la Universidad de San Carlos de Guatemala. Guatemala, 2019 Textos y edición: Manolo J. García. Zoólogo CDC Primera edición, 2019 Centro de Estudios Conservacionistas (Cecon) de la Facultad de Ciencias Químicas y Farmacia de la Universidad de San Carlos de Guatemala ISBN: 978-9929-570-19-1 Cita sugerida: Centro de Estudios Conservacionistas [Cecon]. (2019). Catálogo de autoridades taxonómicas de vertebrados de Guatemala (Documento técnico). Guatemala: Centro de Datos para la Conservación [CDC], Centro de Estudios Conservacionistas [Cecon], Facultad de Ciencias Químicas y Farmacia, Universidad de San Carlos de Guatemala [Usac]. Índice 1. Presentación ............................................................................................ 4 2. Directrices generales para uso del CAT .............................................. 5 2.1 El grupo objetivo ..................................................................... 5 2.2 Categorías taxonómicas ......................................................... 5 2.3 Nombre de autoridades .......................................................... 5 2.4 Estatus taxonómico -
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) -
A Comprehensive Multilocus Phylogeny of the Neotropical Cotingas
Molecular Phylogenetics and Evolution 81 (2014) 120–136 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A comprehensive multilocus phylogeny of the Neotropical cotingas (Cotingidae, Aves) with a comparative evolutionary analysis of breeding system and plumage dimorphism and a revised phylogenetic classification ⇑ Jacob S. Berv 1, Richard O. Prum Department of Ecology and Evolutionary Biology and Peabody Museum of Natural History, Yale University, P.O. Box 208105, New Haven, CT 06520, USA article info abstract Article history: The Neotropical cotingas (Cotingidae: Aves) are a group of passerine birds that are characterized by Received 18 April 2014 extreme diversity in morphology, ecology, breeding system, and behavior. Here, we present a compre- Revised 24 July 2014 hensive phylogeny of the Neotropical cotingas based on six nuclear and mitochondrial loci (7500 bp) Accepted 6 September 2014 for a sample of 61 cotinga species in all 25 genera, and 22 species of suboscine outgroups. Our taxon sam- Available online 16 September 2014 ple more than doubles the number of cotinga species studied in previous analyses, and allows us to test the monophyly of the cotingas as well as their intrageneric relationships with high resolution. We ana- Keywords: lyze our genetic data using a Bayesian species tree method, and concatenated Bayesian and maximum Phylogenetics likelihood methods, and present a highly supported phylogenetic hypothesis. We confirm the monophyly Bayesian inference Species-tree of the cotingas, and present the first phylogenetic evidence for the relationships of Phibalura flavirostris as Sexual selection the sister group to Ampelion and Doliornis, and the paraphyly of Lipaugus with respect to Tijuca. -
Rapid Ecological Assessment Mayflower Bocawina National Park
Rapid Ecological Assessment Mayflower Bocawina National Park Volume II - Appendix J.C. Meerman B. Holland, A. Howe, H. L. Jones, B. W. Miller This report was prepared for: Friends of Mayflower under a grant provided by PACT. July 31, 2003 J. C. Meerman – REA – Mayflower Bocawina National Park – Appendices – July 2003 – page 1 Appendix 1 Birdlist of Mayflower Bocawina National Park (MBNP) Status: R = Resident, W =Winter visitor, D = Drys season resident, A = Accidental visitor, T = Transient. MBNP: X = Recorded during REA, ? = Species in need of confirmation, MN = Reported by Mamanoots Resort, some may need confirmation English Name Scientific name Local name(s) Status MBNP TINAMOUS - TINAMIDAE Great Tinamou Tinamus major Blue-footed partridge R X Little Tinamou Crypturellus soui Bawley R X Slaty-breasted Tinamou Crypturellus boucardi Red-footed partridge R ? HERONS - ARDEIDAE Bare-throated Tiger Heron Tigrisoma mexicanum Barking gaulin R X Great Egret Egretta alba Gaulin, Garza blanca WR MN Little Blue Heron Egretta caerulea Blue Gaulin, Garza morene W X Cattle Egret Bubulcus ibis Gaulin, Garza blanca WR X AMERICAN VULTURES - CATHARTIDAE Black Vulture Coragyps atratus John Crow, Sope WR X Turkey Vulture Cathartes aura Doctor John Crow, Sope WR X King Vulture Sarcoramphus papa King John Crow, Sope real R X KITES, HAWKS, EAGLES AND ALLIES - ACCIPITRIDAE Swallow-tailed Kite Elanoides forficatus Scissors-tailed hawk DT X Plumbeous Kite Ictinia plumbea D MN White Hawk Leucopternis albicollis R X Gray Hawk Asturina nitidus R X Great Black-Hawk -
Boc1282-080509:BOC Bulletin.Qxd
boc1282-080509:BOC Bulletin 5/9/2008 7:22 AM Page 107 Andrew Whittaker 107 Bull. B.O.C. 2008 128(2) Field evidence for the validity of White- tailed Tityra Tityra leucura Pelzeln, 1868 by Andrew Whittaker Received 30 March 2007; final revision received 28 February 2008 Tityra leucura (White- tailed Tityra) was described by Pelzeln (1868) from a specimen collected by J. Natterer, on 8 October 1829, at Salto do Girao [=Salto do Jirau] (09º20’S, 64º43’W) c.120 km south- west of Porto Velho, the capital of Rondônia, in south- central Amazonian Brazil (Fig 1). The holotype is an immature male and is housed in Vienna, at the Naturhistorisches Museum Wien (NMW 16.999). Subsequent authors (Hellmayr 1910, 1929, Pinto 1944, Peters 1979, Ridgely & Tudor 1994, Fitzpatrick 2004, Mallet- Rodrigues 2005) have expressed severe doubts concerning this taxon’s validity, whilst others simply chose to ignore it (Sick 1985, 1993, 1997, Collar et al. 1992.). Almost 180 years have passed since its collection with the result that T. leucura has slipped into oblivion, and the majority of Neotropical ornithologists and birdwatchers are unaware of its existence. Here, I review the history of T. leucura and then describe its rediscovery from the rio Madeira drainage of south- central Amazonian Brazil, providing details of my field observa- tions of an adult male. I present the first published photographs of the holotype of T. leucura, and compare plumage and morphological differences with two similar races of Black- crowned Tityra T. inquisitor pelzelni and T. i. albitorques. T. inquisitor specimens were examined at two Brazilian museums for abnormal plumage characters. -
Species List January 28 – February 6, 2020 | Compiled by Keith Hansen
Guatemala: Nature & Culture With Tikal Extension| Species List January 28 – February 6, 2020 | Compiled by Keith Hansen With Guides Keith Hansen, Patricia Briceño, Roland Rumm and local guide Freddie and participants Julie, Paul, Gwen, Gary, Barbara, Rolande, Brian, Jane, and Debbie. Itinerary Day 1: 1/29/20, Guatemala City. Clarion Hotel to Marroquin University and Textile Museum, to Guatemala Market, to Cocales “Crazy Gas Station” at intersection of CA 12 and 11 to Los Tarrales Natural Reserve. Day 2: 1/30/20, Los Tarrales Nat. Res. into jeeps and up to La Isla vista point. Down for lunch at lodge. Then San Pedro trail and back to La Rinconada lodge, for dinner. Day 3: 1/31/20, Pre-dawn, Volcan Fuego eruption. Los Tarrales, short walk on San Pedro Trail. Breakfast at lodge. Depart and drive to Fuentes Georginia Hot Springs Spa. Lunch with “mega flock”. Depart and drive to Xela (Quetzaltenango). Dinner at Hotel Bonifaz. Day 4: 2/1/20, Split group. One group, (Keith), up at 4:00 AM. Drive to Refugio del Quetzal for Quetzal, then viewing from mirador “overlook”. Then drive to San Rafael for lunch. Then drive back to Xela. Second group, (Patricia) Xela tour. Later some went back to “Owl” at Fuentes Georgino Hot Springs, then back to Xela. Day 5: 2/2/20, Xela breakfast at Hotel, depart for the market at Chichicastenango with stop at Continental Divide at 10,000 feet. To market, then lunch at “Mayan Inn”. Drive to Panajachel at Lago de Atitlan. Boarded a launch to cross the lake to Hotel Bambu, Santiago Atitlan. -
Master Thesis
The effect of foraging ecology on the onset of dawn song for passerine species Marte Ulltang Master of Science in Biology Biodiversity, Evolution and Ecology Department of Biological Sciences University of Bergen 20.11.2018 «tsip-prrup, tsip-prrup-prrup, tsip-prrup, tsip-prrup-prrup-prrup, tsip-prrup-prrup, tsip-prrup-prrup-prrup-prrup» Dawn song of the tree swallow (Tachycineta bicolor) Allen (1913) Front cover photo. https://pxhere.com/en/photo/583817 (CC0 1.0) https://creativecommons.org/publicdomain/zero/1.0/ II Acknowledgements First and foremost, I would like to thank my supervisors Sigrunn Eliassen and Christian Jørgensen for guidance, feedback and support throughout this project, and for giving me the opportunity to work with the intriguing dawn chorus. In addition, I am grateful to Julianne Netteland for collaboration, conversations and exchange of knowledge. I am deeply grateful to Melissah Rowe for welcoming me when I moved to Oslo, and for introducing me to Jan T. Lifjeld and the Sex and Evolution Research Group (SERG) at Natural History Museum in Oslo. I would like to thank SERG for including me in their research group, and for giving me advice and suggestions. I would like to express my gratitude to my wonderful family for love, support and motivation, and my best friend Pomba, for always being there for me. I am grateful for my beloved sister and proofreader Synne Ulltang. I want to thank all my friends during my studies, for euncouraging and inspiring me. A special thanks to Randi Elisabeth Åsly for proofreading my thesis. I am very thankful for our friendship and shared enthusiasm for evolution. -
Checklistccamp2016.Pdf
2 3 Participant’s Name: Tour Company: Date#1: / / Tour locations Date #2: / / Tour locations Date #3: / / Tour locations Date #4: / / Tour locations Date #5: / / Tour locations Date #6: / / Tour locations Date #7: / / Tour locations Date #8: / / Tour locations Codes used in Column A Codes Sample Species a = Abundant Red-lored Parrot c = Common White-headed Wren u = Uncommon Gray-cheeked Nunlet r = Rare Sapayoa vr = Very rare Wing-banded Antbird m = Migrant Bay-breasted Warbler x = Accidental Dwarf Cuckoo (E) = Endemic Stripe-cheeked Woodpecker Species marked with an asterisk (*) can be found in the birding areas visited on the tour outside of the immediate Canopy Camp property such as Nusagandi, San Francisco Reserve, El Real and Darien National Park/Cerro Pirre. Of course, 4with incredible biodiversity and changing environments, there is always the possibility to see species not listed here. If you have a sighting not on this list, please let us know! No. Bird Species 1A 2 3 4 5 6 7 8 Tinamous Great Tinamou u 1 Tinamus major Little Tinamou c 2 Crypturellus soui Ducks Black-bellied Whistling-Duck 3 Dendrocygna autumnalis u Muscovy Duck 4 Cairina moschata r Blue-winged Teal 5 Anas discors m Curassows, Guans & Chachalacas Gray-headed Chachalaca 6 Ortalis cinereiceps c Crested Guan 7 Penelope purpurascens u Great Curassow 8 Crax rubra r New World Quails Tawny-faced Quail 9 Rhynchortyx cinctus r* Marbled Wood-Quail 10 Odontophorus gujanensis r* Black-eared Wood-Quail 11 Odontophorus melanotis u Grebes Least Grebe 12 Tachybaptus dominicus u www.canopytower.com 3 BirdChecklist No. -
The All-Bird Bulletin
Advancing Integrated Bird Conservation in North America Spring 2014 Inside this issue: The All-Bird Bulletin Protecting Habitat for 4 the Buff-breasted Sandpiper in Bolivia The Neotropical Migratory Bird Conservation Conserving the “Jewels 6 Act (NMBCA): Thirteen Years of Hemispheric in the Crown” for Neotropical Migrants Bird Conservation Guy Foulks, Program Coordinator, Division of Bird Habitat Conservation, U.S. Fish and Bird Conservation in 8 Wildlife Service (USFWS) Costa Rica’s Agricultural Matrix In 2000, responding to alarming declines in many Neotropical migratory bird popu- Uruguayan Rice Fields 10 lations due to habitat loss and degradation, Congress passed the Neotropical Migra- as Wintering Habitat for tory Bird Conservation Act (NMBCA). The legislation created a unique funding Neotropical Shorebirds source to foster the cooperative conservation needed to sustain these species through all stages of their life cycles, which occur throughout the Western Hemi- Conserving Antigua’s 12 sphere. Since its first year of appropriations in 2002, the NMBCA has become in- Most Critical Bird strumental to migratory bird conservation Habitat in the Americas. Neotropical Migratory 14 Bird Conservation in the The mission of the North American Bird Heart of South America Conservation Initiative is to ensure that populations and habitats of North Ameri- Aros/Yaqui River Habi- 16 ca's birds are protected, restored, and en- tat Conservation hanced through coordinated efforts at in- ternational, national, regional, and local Strategic Conservation 18 levels, guided by sound science and effec- in the Appalachians of tive management. The NMBCA’s mission Southern Quebec is to achieve just this for over 380 Neo- tropical migratory bird species by provid- ...and more! Cerulean Warbler, a Neotropical migrant, is a ing conservation support within and be- USFWS Bird of Conservation Concern and listed as yond North America—to Latin America Vulnerable on the International Union for Conser- Coordination and editorial vation of Nature (IUCN) Red List. -
Tinamiformes – Falconiformes
LIST OF THE 2,008 BIRD SPECIES (WITH SCIENTIFIC AND ENGLISH NAMES) KNOWN FROM THE A.O.U. CHECK-LIST AREA. Notes: "(A)" = accidental/casualin A.O.U. area; "(H)" -- recordedin A.O.U. area only from Hawaii; "(I)" = introducedinto A.O.U. area; "(N)" = has not bred in A.O.U. area but occursregularly as nonbreedingvisitor; "?" precedingname = extinct. TINAMIFORMES TINAMIDAE Tinamus major Great Tinamou. Nothocercusbonapartei Highland Tinamou. Crypturellus soui Little Tinamou. Crypturelluscinnamomeus Thicket Tinamou. Crypturellusboucardi Slaty-breastedTinamou. Crypturellus kerriae Choco Tinamou. GAVIIFORMES GAVIIDAE Gavia stellata Red-throated Loon. Gavia arctica Arctic Loon. Gavia pacifica Pacific Loon. Gavia immer Common Loon. Gavia adamsii Yellow-billed Loon. PODICIPEDIFORMES PODICIPEDIDAE Tachybaptusdominicus Least Grebe. Podilymbuspodiceps Pied-billed Grebe. ?Podilymbusgigas Atitlan Grebe. Podicepsauritus Horned Grebe. Podicepsgrisegena Red-neckedGrebe. Podicepsnigricollis Eared Grebe. Aechmophorusoccidentalis Western Grebe. Aechmophorusclarkii Clark's Grebe. PROCELLARIIFORMES DIOMEDEIDAE Thalassarchechlororhynchos Yellow-nosed Albatross. (A) Thalassarchecauta Shy Albatross.(A) Thalassarchemelanophris Black-browed Albatross. (A) Phoebetriapalpebrata Light-mantled Albatross. (A) Diomedea exulans WanderingAlbatross. (A) Phoebastriaimmutabilis Laysan Albatross. Phoebastrianigripes Black-lootedAlbatross. Phoebastriaalbatrus Short-tailedAlbatross. (N) PROCELLARIIDAE Fulmarus glacialis Northern Fulmar. Pterodroma neglecta KermadecPetrel. (A) Pterodroma