Diurnal Birds of Prey of Belize
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2016 Checklist of Florida'a Birds
Artwork by Ann Marie Tavares 2016 Checklist of Florida’s Birds Prepared by Dr. Greg Schrott and Andy Wraithmell The Florida Fish and Wildlife Conservation Commission Florida’s wild places are home to an incredible diversity of birds. Over 500 native bird species or naturally occurring strays have been recorded in the state in historic times, and about 330 native species commonly occur here (four have gone extinct). A further 14 nonnative species are considered to have established large, stable populations in Florida. More than 70 natural community types support this diversity, from the pine flatwoods of Apalachicola National Forest, to the scrub communities of the Lake Wales Ridge, and the vast sawgrass marshes and mangrove swamps of Everglades National Park. Our natural areas harbor many bird species seen nowhere else in the United States such as the Florida Scrub-Jay, Mangrove Cuckoo, and Snail Kite. In addition, Florida’s birdlife changes with the cycle of the seasons. A constant turnover of breeding, wintering and migratory species provides new birding experiences throughout the year. To help you keep track of the spectacular range of birdlife the state has to offer, the Florida Fish and Wildlife Conservation Commission (FWC) has published this checklist. The first edition of Checklist of Florida’s Birds was prepared by Dr. Henry M. Stevenson in 1986. During his lifetime, Dr. Stevenson made many contributions to the field of ornithology, culminating with his writing The Birdlife of Florida with Bruce H. Anderson (1994). This book offers the most comprehensive information published on the lives of Florida’s birds. -
Arizona Game and Fish Department Heritage Data Management System
ARIZONA GAME AND FISH DEPARTMENT HERITAGE DATA MANAGEMENT SYSTEM Animal Abstract Element Code: ABNKC15010 Data Sensitivity: Yes CLASSIFICATION, NOMENCLATURE, DESCRIPTION, RANGE NAME: Buteogallus anthracinus Deppe COMMON NAME: Common black-hawk, Lesser black hawk, Mexican black hawk, crab hawk, Sparrowhawk Black Crab seller, Sparrowhawk Crab seller, Aguililla-negra menor (Spanish) SYNONYMS: Falco anthracinus, Buteogallus anthracinus anthracinus FAMILY: Accipitridae AUTHOR, PLACE OF PUBLICATION: W. Deppe, Preis-Verz. Saugheth. Vog…Mexico. Pp: 3. 1830. TYPE LOCALITY: TYPE SPECIMEN: TAXONOMIC UNIQUENESS: The species anthracinus is 1 of 5 within the genus Buteogallus , and is divided into 3 subspecies, B.a. bangsi , found on Cuba and Isle of Pines; B.a. utilensis farther south on islands in the Gulf of Honduras and B.a. anthracinus from northern South America to the southwestern United States (Schnell et al. 1986). DESCRIPTION: A medium to large-sized hawk with broad rounded wings, and a hooked beak. The length is 20-22 inches (51-56 cm), wingspan 40-50 inches (102-127 cm), and a weight of 1.4-2.9 lbs (0.6-1.3 kg). As with most other raptor species, Common Black-hawks are sexually dimorphic, with the females being larger than the males. Adults are uniformly blackish except for the white 1-3 inch-wide median band on the short broad tail, which is the most distinctive identification mark for this species. The small white base of primaries, are not always visible. The sexes are similar and cannot be distinguished in the field with certainty except by behavioral differences, although many females have a longer light patch in the malar region below the eye. -
Chromosome Painting in Three Species of Buteoninae: a Cytogenetic Signature Reinforces the Monophyly of South American Species
Chromosome Painting in Three Species of Buteoninae: A Cytogenetic Signature Reinforces the Monophyly of South American Species Edivaldo Herculano C. de Oliveira1,2,3*, Marcella Mergulha˜o Tagliarini4, Michelly S. dos Santos5, Patricia C. M. O’Brien3, Malcolm A. Ferguson-Smith3 1 Laborato´rio de Cultura de Tecidos e Citogene´tica, SAMAM, Instituto Evandro Chagas, Ananindeua, PA, Brazil, 2 Faculdade de Cieˆncias Exatas e Naturais, ICEN, Universidade Federal do Para´, Bele´m, PA, Brazil, 3 Cambridge Resource Centre for Comparative Genomics, Cambridge, United Kingdom, 4 Programa de Po´s Graduac¸a˜oem Neurocieˆncias e Biologia Celular, ICB, Universidade Federal do Para´, Bele´m, PA, Brazil, 5 PIBIC – Universidade Federal do Para´, Bele´m, PA, Brazil Abstract Buteoninae (Falconiformes, Accipitridae) consist of the widely distributed genus Buteo, and several closely related species in a group called ‘‘sub-buteonine hawks’’, such as Buteogallus, Parabuteo, Asturina, Leucopternis and Busarellus, with unsolved phylogenetic relationships. Diploid number ranges between 2n = 66 and 2n = 68. Only one species, L. albicollis had its karyotype analyzed by molecular cytogenetics. The aim of this study was to present chromosomal analysis of three species of Buteoninae: Rupornis magnirostris, Asturina nitida and Buteogallus meridionallis using fluorescence in situ hybridization (FISH) experiments with telomeric and rDNA probes, as well as whole chromosome probes derived from Gallus gallus and Leucopternis albicollis. The three species analyzed herein showed similar karyotypes, with 2n = 68. Telomeric probes showed some interstitial telomeric sequences, which could be resulted by fusion processes occurred in the chromosomal evolution of the group, including the one found in the tassociation GGA1p/GGA6. -
Field Identification of the Field Identification of the Field
TOPICS IN IDENTIFICATION he Solitary Eagle ( Harpyhaliaetus solitarius ) is a large raptor that is closely related and similar in adult and immature plum- Tages to the black-hawks in the genus Buteogallus (Lerner and Mindell 2005). It is a rare and very local resident in a variety of wet and dry forested hills and highlands from northern Argentina to northern Mexico (del Hoyo et al. 1994, Ferguson-Lees and Christie 2001). The species has been collected in Mexico not far from the Texas border (see Discussion, pp. 72 –73), so it is possible that it has occurred in the ABA Area. The handful of specimens and nest records of this eagle are from 700 to 2,000 meters above sea level (Brown and Amadon 1968). FFiieelldd IIddeennttiifificcaattiioonn ooff tthhee SSOOLLIITTTAAARRRYYY EEAAAGGGLLLEEE Nevertheless, sightings of this eagle are occasionally reported from lowland tropical rain forest, e.g., at Tikal, Guatemala (Beaver et al. 1991) and the Tuxtlas Mountains of south - William S. Clark ern Veracruz, Mexico (Winker et al. 1992). The species has been reported on some pro - 2301 South Whitehouse Circle fessional bird tours at such lowland sites as Palenque and the Usumicinta River in south - Harlingen, Texas 78550 ern Mexico. All of these accounts have relied on large size and gray coloration as the [email protected] field marks to distinguish the eagles from the much more abundant Common Black- Hawk ( Buteogallus anthracinus ) and Great Black-Hawk ( B. urubitinga ). H. Lee Jones Howell and Webb (1995) were skeptical and stated that most lowland records of the 4810 Park Newport, No. -
The Evolution of Nest Construction in Swallows (Hirundinidae) Is Associated with the Decrease of Clutch Size
© Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Linzer biol. Beitr. 38/1 711-716 21.7.2006 The evolution of nest construction in swallows (Hirundinidae) is associated with the decrease of clutch size P. HENEBERG A b s t r a c t : Variability of the nest construction in swallows (Hirundinidae) is more diverse than in other families of oscine birds. I compared the nest-building behaviour with pooled data of clutch size and overall hatching success for 20 species of swallows. The clutch size was significantly higher in temperate cavity-adopting swallow species than in species using other nesting modes including species breeding in evolutionarily advanced mud nests (P<0.05) except of the burrow-excavating Bank Swallow. Decrease of the clutch size during the evolution of nest construction is not compensated by the increase of the overall hatching success. K e y w o r d s : Hirundinidae, nest construction, clutch size, evolution Birds use distinct methods to avoid nest-predation: active nest defence, nest camouflage and concealment or sheltered nesting. While large and powerful species prefer active nest-defence, swallows and martins usually prefer construction of sheltered nests (LLOYD 2004). The nests of swallows vary from natural cavities in trees and rocks, to self-exca- vated burrows to mud retorts and cups attached to vertical faces. Much attention has been devoted to the importance of controlling for phylogeny in com- parative tests (HARVEY & PAGEL 1991), including molecular phylogenetic studies of swallows (WINKLER & SHELDON 1993). Interactions between the nest-construction va- riability and the clutch size, however, had been ignored. -
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. -
O Mimetismo Das Serpentes Corais Em Ambientes
UNIVERSIDADE DE BRASÍLIA INSTITUTO DE CIÊNCIAS BIOLÓGICAS DEPARTAMENTO DE ECOLOGIA O MIMETISMO DAS SERPENTES CORAIS EM AMBIENTES CAMPESTRES, SAVÂNICOS E FLORESTAIS DA AMÉRICA DO SUL Frederico Gustavo Rodrigues França Brasília-DF 2008 UNIVERSIDADE DE BRASÍLIA INSTITUTO DE CIÊNCIAS BIOLÓGICAS DEPARTAMENTO DE ECOLOGIA O MIMETISMO DAS SERPENTES CORAIS EM AMBIENTES CAMPESTRES, SAVÂNICOS E FLORESTAIS DA AMÉRICA DO SUL Frederico Gustavo Rodrigues França Orientador: Alexandre Fernandes Bamberg de Araújo Tese apresentada ao Departamento de Ecologia do Instituto de Ciências Biológicas da Universidade de Brasília, como parte dos requisitos necessários para a obtenção do título de Doutor em Ecologia. Brasília-DF 2008 Trabalho realizado junto ao Departamento de Ecologia do Instituto de Ciências Biológicas da Universidade de Brasília, sob orientação do Prof. Alexandre Fernandes Bamberg de Araújo, com o apoio financeiro da Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) e Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), como parte dos requisitos para obtenção do título de Doutor em Ecologia. Data da Defesa: 01 de agosto de 2008 Banca Examinadora Prof. Dr. Alexandre Fernandes Bamberg de Araújo (Orientador) ________________________________________________ Prof. Dr. Daniel Oliveira Mesquita ________________________________________________ Prof. Dr. Guarino Rinaldi Colli ________________________________________________ Prof. Dr. Hélio Ricardo da Silva ________________________________________________ Prof. Dr. Raimundo -
Extreme Variation in the Tails of Adult Harlan’S Hawks
EXTREME VARIATION IN THE TAILS OF ADULT HARLAN’S HAWKS William S. (Bill) Clark Some adult Harlan’s Hawks have tails somewhat similar to this one Bob Dittrick But many others have very different tails, both in color and in markings Harlan’s Hawk type specimen. Audubon collected this adult in 1830 in Louisiana (USA) and described it as Harlan’s Buzzard or Black Warrier - Buteo harlani It is a dark morph, the common morph for this taxon. British Museum of Natural History, Tring Harlan’s Hawk Range They breed in Alaska, Yukon, & ne British Columbia & winter over much of North America. It occurs in two color morphs, dark and light. The AOS considers Harlan’s Hawk a subspecies of Red- tailed Hawk, Buteo jamaicensis harlani, but my paper in Zootaxa advocates it as a species. Clark (2018) Taxonomic status of Harlan’s Hawk Buteo jamaicensis harlani (Aves: Accipitriformes) Zootaxa concludes: “It [Harlan’s Hawk] should be considered a full species based on lack of justification for considering it a subspecies, and the many differences between it and B. jamaicensis, which are greater than differences between any two subspecies of diurnal raptor.” Harlan’s Hawk is a species: 1. Lack of taxonomic justification for inclusion with Buteo jamaicensis. 2. Differs from Buteo jamaicensis by: * Frequency of color morphs; * Adult plumages by color morph, especially in tail pattern and color; * Neotony: Harlan’s adult & juvenile body plumages are almost alike; whereas those of Red-tails differ. * Extent of bare area on the tarsus. * Some behaviors. TYPE SPECIMEN - Upper tail is medium gray, with a hint of rufous and some speckling, wavy banding on one feather, & wide irregular subterminal band. -
Predation of Birds Trapped in Mist Nets by Raptors in the Brazilian Caatinga
Predation of Birds Trapped in Mist Nets by Raptors in the Brazilian Caatinga 1 2 5 Juan Ruiz-Esparza • • Resumen: 1 3 Patricio Adriano da Rocha • La red de neb/ina es una tecnica de captura de Adauto de Souza Ribeiro4 vertebrados voladores como aves y murcielagos. Una Stephen F. Ferrari4 vez capturados e inmovilizados, los animates son 1 Graduate Program in Ecology and Conservation, vulnerables a ataques par predadores hasta su extracci6n. Ataques de animates atrapados han sido Universidade Federal de Sergipe, Avenida registrados en diferentes lugares, aunque los datos son Marechal Rondon s/n, 49.100-000 Sao poco sistematicos, tales como clasificaci6n de la Crist6vao - Sergipe, Brazil. depredaci6n estrin disponibles. Analizamos ataques 2 PR D MA , Universidade Federal de Sergipe, contra las aves capturadas en redes de neblina en la Av. Marechal Rondon s/n, 49.100-000 Caatinga y regiones aledafias en el nordeste de Brasil. Sao Crist6vao-Sergipe, Brazil. Un total de 979 aves fueron capturadas durante 6, 000 horas-red de muestreo, donde 18 (1, 8%) fueron 3 Graduate Program in Zoot gy, U n:i versidade encontradas muertas en Ia red de neblina con senates de Federal da Paraiba, Joao Pessoa-Paraiba, Brazil. Ia depredaci6n. En Ia mayoria de los casas no fue posible identificar el predador, un Gavilan de los 4 Department of Biology, Unjversidade Fed ral d Caminos (Rupomis magnirostris) fue capturado junto S r0 ipe, A venida Marechal Rondon con un Chivi Amarillento (Basileuterus flaveolus) /n 49.100-000 Sao Crist6vao- Sergipe Brazil. depredado, heridas simi/ares fueron observadas en las 5 orresponding author; e-maiJ: otras aves, sugiriendo que rapaces pudieron haber sido juanco lorad 2 1@ h tmail.com responsables par los otros ataques. -
Trinidad & Tobago 2018 Species List
Trinidad Tobago Leader: Ernesto Carman Eagle-Eye Tours Nov 29 - Dec 9, 2018 Bird Species Seen/ Common Name Scientific Name Heard TINAMOUS 1 Little Tinamou Crypturellus soui H GUANS, CHACHALACAS, AND CURASSOWS 2 Trinidad Piping-Guan Aburria pipile S 3 Rufous-vented Chachalaca Ortalis ruficauda S FLAMINGOS 4 American Flamingo Phoenicopterus ruber S TROPICBIRDS 5 Red-billed Tropicbird Phaethon aethereus S FRIGATEBIRDS 6 Magnificent Frigatebird Fregata magnificens S BOOBIES AND GANNETS 7 Brown Booby Sula leucogaster S 8 Red-footed Booby Sula sula S CORMORANTS AND SHAGS 9 Neotropic Cormorant Phalacrocorax brasilianus S ANHINGAS 10 Anhinga Anhinga anhinga S PELICANS 11 Brown Pelican Pelecanus occidentalis S HERONS, EGRETS, AND BITTERNS 12 Pinnated Bittern Botaurus pinnatus S 13 Great Egret Ardea alba S 14 Little Egret Egretta garzetta S 15 Snowy Egret Egretta thula S 16 Little Blue Heron Egretta caerulea S 17 Tricolored Heron Egretta tricolor S 18 Cattle Egret Bubulcus ibis S 19 Green Heron Butorides virescens S 20 Striated Heron Butorides striata S 21 Black-crowned Night-Heron Nycticorax nycticorax S 22 Yellow-crowned Night-Heron Nyctanassa violacea S 23 Boat-billed Heron Cochlearius cochlearius S IBISES AND SPOONBILLS 24 Scarlet Ibis Eudocimus ruber S NEW WORLD VULTURES Page 1 of 8 www.eagle-eye.com Trinidad Tobago Leader: Ernesto Carman Eagle-Eye Tours Nov 29 - Dec 9, 2018 Bird Species Seen/ Common Name Scientific Name Heard 25 Black Vulture Coragyps atratus S 26 Turkey Vulture Cathartes aura S OSPREY 27 Osprey Pandion haliaetus S HAWKS, -
Estimations Relative to Birds of Prey in Captivity in the United States of America
ESTIMATIONS RELATIVE TO BIRDS OF PREY IN CAPTIVITY IN THE UNITED STATES OF AMERICA by Roger Thacker Department of Animal Laboratories The Ohio State University Columbus, Ohio 43210 Introduction. Counts relating to birds of prey in captivity have been accomplished in some European countries; how- ever, to the knowledge of this author no such information is available in the United States of America. The following paper consistsof data related to this subject collected during 1969-1970 from surveys carried out in many different direc- tions within this country. Methods. In an attempt to obtain as clear a picture as pos- sible, counts were divided into specific areas: Research, Zoo- logical, Falconry, and Pet Holders. It became obvious as the project advanced that in some casesthere was overlap from one area to another; an example of this being a falconer working with a bird both for falconry and research purposes. In some instances such as this, the author has used his own judgment in placing birds in specific categories; in other in- stances received information has been used for this purpose. It has also become clear during this project that a count of "pets" is very difficult to obtain. Lack of interest, non-coop- eration, or no available information from animal sales firms makes the task very difficult, as unfortunately, to obtain a clear dispersal picture it is from such sourcesthat informa- tion must be gleaned. However, data related to the importa- tion of birds' of prey as recorded by the Bureau of Sport Fisheries and Wildlife is included, and it is felt some observa- tions can be made from these figures. -
I POPULATION SIZE of BLUE-FOOTED BOOBIES IN
POPULATION SIZE OF BLUE-FOOTED BOOBIES IN GALÁPAGOS: EVALUATION OF INDICATIONS OF POPULATION DECLINE BY DAVID ANCHUNDIA A Thesis Submitted to the Graduate Faculty of WAKE FOREST UNIVERSITY GRADUATE SCHOOL OF ARTS AND SCIENCES in Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Biology May 2013 Winston-Salem, North Carolina Approved By: David J. Anderson, Ph.D., Advisor Miles R. Silman, Ph.D., Chair Todd M. Anderson, Ph.D. i DEDICATION This work is dedicated to the memory of my loving mother Juana Isabel Gonzalez. I thank her for all the support and the encouragement she gave me to study sciences. Also I thank my father Oswaldo Anchundia for his constant support during all this time. I will always appreciate all that they have done for me; this degree is dedicated to them. David J. Anchundia Gonzalez ii ACKNOWLEDGEMENT I want to express my sincere gratitude to my advisor Prof. David John Anderson for all the advice, motivation, enthusiasm, and immense knowledge that he shared with me during my M. S. study and research. Also I thank my lab mates Jacquelyn Grace, Felipe Estela, Emily Tompkins, and Terri Mannes for the help and guidance in my research. I want to thank the Prof. Miles Silman and Prof. Michael Anderson, who were part of my thesis committee, and the Professors of the Biology Department from Wake Forest University who shared their knowledge with me. I would like to express my gratitude to: Prof. Kathryn Huyvaert from Colorado State University, who helped me in parts of the analysis and modeling parts of the project; Kyle Anderson from Idaho State University, who helped with part of the GIS analysis; Professors Peter and Rosemary Grant from Princeton University, who provided unpublished breeding and attendance data from Daphne Island; and Lisa Balance and Robert Pitman from the National Marine Fisheries Service (La Jolla) for sharing unpublished at-sea distribution data.