Comparison of Fossil and Recent Species: Some Difficulties
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(Buteogallus Coronatus) in Argentina
SHORT COMMUNICATIONS J. Raptor Res. 54(2):166–171 Ó 2020 The Raptor Research Foundation, Inc. ELECTROCUTION ON POWER LINES IS AN IMPORTANT THREAT FOR THE ENDANGERED CHACO EAGLE (BUTEOGALLUS CORONATUS) IN ARGENTINA 1 JOSE´ H. SARASOLA Centro para el Estudio y Conservacio´n de Aves Rapaces en Argentina (CECARA). Universidad Nacional de La Pampa, Avda Uruguay 151, 6300 Santa Rosa, Argentina and Instituto de las Ciencias Ambientales y de la Tierra de La Pampa (INCITAP-CONICET), Avda Uruguay 151, 6300 Santa Rosa, La Pampa, Argentina MAXIMILIANO A. GALMES Centro para el Estudio y Conservacio´n de Aves Rapaces en Argentina (CECARA), Universidad Nacional de La Pampa, Avda Uruguay 151, 6300 Santa Rosa, Argentina and The Peregrine Fund, Boise, ID 83709 USA BRYAN D. WATTS Center for Conservation Biology, College of William & Mary, Williamsburg, VA 23187 USA and Virginia Commonwealth University, Williamsburg, VA 23284 USA ABSTRACT.—Electrocution is a widespread conservation problem for birds of prey that has received little attention in the Neotropics. Here we present electrocution records involving the endangered Chaco Eagle (Buteogallus coronatus) in central Argentina, and we provide information on the power pole structural characteristics associated with electrocutions. Nine Chaco Eagles were recorded electrocuted during the period 2012–2019 over an area of 9000 km2. Chaco Eagles were found electrocuted in association with five types of power poles, but more than half the electrocutions (55%) were on poles made of steel-reinforced concrete and with jumper wires above the crossarms. With the addition of four previous electrocution reports in this region during the same time period, the annual rate of Chaco Eagle electrocutions was similar to the rate of mortality by other human-related factors such as direct persecution. -
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) -
White-Tailed Hawk (Geranoaetus Albicaudatus)
D. Oleyar, D. Ethier, L. Goodrich, D. Brandes, R. Smith, J. Brown, and J. Sodergren. 2021. The Raptor Population Index: 2019 Analyses and Assessments. Available at http://rpi-project.org/2019/assessments2019.php Introduction to North American Raptor Conservation Species Assessments We provide species assessments based on trend analyses through 2019 from 76 raptor migration count sites across North America spanning from Canada to Panama. Synthesis of trends at the continental and regional scales can highlight species and/or regions that warrant a closer look in the case of widespread declines or highlight conservation successes in the case of widespread increases. It is important to note that the intent of long-term monitoring efforts like RPI is to identify changes overtime, not necessarily to explain them—that is where focused research efforts come into play. RPI shines a light on species and places in need of closer looks and focused efforts. In these assessments, we provide a summary of the continental and regional migration count trends for each species and highlight species of concern. For complete and/or long-distance migrants such as Osprey, Broad-winged Hawk, Swainson’s Hawk, and Mississippi Kite, where essentially the entire population migrates out of its breeding range to a separate wintering range, the migration count trends provide a reliable assessment of actual population trends. For partial and short-distance migrants such as the Red-tailed Hawk, there is evidence that some species may be shifting their migratory behavior and/or wintering ranges in response to climate change and other factors (Bolgiano, 2013; Paprocki, et al, 2017). -
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. -
Application for Non-Resident Raptor Trapping Permit
Application for Non-Resident Raptor Trapping Permit Please complete this form and return it, along with the permit fee and requested attachments, to: Texas Parks and Wildlife Department, Wildlife Diversity Permits, 4200 Smith School Road, Austin, TX 78744. All applicants for a Non-Resident Raptor Trapping Permit must possess a permit from their home state equivalent to a Texas Apprentice, General or Master Falconer permit. A non-resident shall not st th trap more than one raptor per year in this state (July 1 – June 30 ). Applicant Name: Home Phone: Office Phone: Street Address: Cell Phone: Driver's License No.: City: State: Zip: Date of Birth: 1 Social Security E-mail Address: Number: 1. This application is for a Non-Resident Raptor Trapping Permit to allow a permitted non-resident apprentice, general or master falconer to take, from the wild in Texas with a valid non-resident hunting license, one of the following species of raptors within the permit year (July 1st – June 30th): Sharp-shinned hawk (Accipiter striatus), Cooper’s hawk (Accipiter cooperii), Harris’s Hawk (Parabuteo unicinctus), Red-shouldered hawk (Buteo lineatus), Red-tailed hawk (Buteo jamaicensis), Ferruginous hawk (Buteo regalis), American kestrel (Falco sparverius), Merlin (Falco columbarius), Prairie falcon (Falco mexicanus), Gyrfalcon (Falco rusticolus), or Caracara (Caracara cheriway). 2. Please attach a copy of your current state falconry permit. 3. Please enclose the $378.00 application and permit fee. (Make checks or money order payable to Texas Parks and Wildlife Department) The Texas Administrative Code Raptor Proclamation can be found online at: http://texreg.sos.state.tx.us/public/readtac$ext.ViewTAC?tac_view=5&ti=31&pt=2&ch=65&sch=K&rl=Y I have read and understand the state regulations titled “Raptor Proclamation” and I will comply with all state and federal laws pertaining to falconry. -
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. -
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. -
The Plate-Billed Mountain Toucan (Andigena Laminirostris) Feeding on a Caecilia Spp (Gymnophiona: Amphibia)
Solano-Ugalde 43 Boletín SAO Vol. 20 Toucans feeding on a Caecilia (No. 2) – Pag: 43-45 ! The Plate-billed Mountain Toucan (Andigena laminirostris) feeding on a Caecilia spp (Gymnophiona: Amphibia) EL TUCÁN ANDINO PIQUILAMINADO (ANDIGENA LAMINIROSTRIS) ALIMENTÁNDOSE DE UN CAECILIA SP (GYMNOPHIONA: AMPHIBIA) Alejandro Solano-Ugalde1,2 1Fundación Imaymana, Paltapamba 476 San Pedro del Valle Nayón, Quito, Ecuador. 2Natural History of Ecuadorian Mainland Avifauna Group, 721 Foch y Amazonas, Quito, Ecuador. E-mail: [email protected] Abstract In this note I report a feeding event of two Plate-billed Mountain Toucans (Andigena laminirostris) upon a Caecilian. Overall, caecilians are poorly known; however at least another bird (Leucopternis princeps) has also been reported feeding on them. As predation was not observed, and based on the corpse state it is likely that the prey was killed prior to the take of the toucans. Keywords: behavior, diet, Ecuador, mountain toucan, new record. Resumen En esta nota reporto dos individuos del Tucán Andino Piquilaminado (Andigena laminirostris) que fueron observados comiendo a un Caecilia spp. Las cecilias son poco conocidos, sin embargo hay registros de otraespecie de ave (Leucopternis princeps) alimentándose de ellos. Ya que la depredación no fue observada, y dado el estado del cadáver, es posible que la presa haya sido matada antes de que los tucanes la tomaran. Palabras clave: comportamiento, dieta, Ecuador, nuevo registro, tucán andino. he genus Andigena (mountain-toucans) comprises On 29 October 2007, while conducting a biological T only four species confined to the northern Andes of survey along the Bellavista Research Station Road South America (Fjeldså & Krabbe 1990). -
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. -
Reproduction and Behaviour of the Long-Legged Buzzard (.Buteo Rufinus) in North-Eastern Greece
© Deutschen Ornithologen-Gesellschaft und Partner; download www.do-g.de; www.zobodat.at Die Vogelwarte 39, 1998: 176-182 Reproduction and behaviour of the Long-legged Buzzard (.Buteo rufinus) in North-eastern Greece By Haralambos Alivizatos, Vassilis Goutner and Michael G. Karandinos Abstract: Alivizatos , H., V. Goutner & M. G. Karandinos (1998): Reproduction and behaviour of the Long- legged Buzzard ( Buteo rufinus) in North-eastern Greece. Vogelwarte 39: 176-182. The breeding biology of the Long-legged Buzzard ( Buteo rufinus) was studied in the Evros area, north-eastern Greece in 1989, 1990, 1992 and 1993. The mean number of young fledged per pair per year was similar between years with an overall average of 0.93 (1.58 per successful pair). Of ten home range variables examined, the num ber of alternative nest sites and the extent of forest free areas in home ranges were significant predictors of nest ling productivity. Aggressive interactions were observed with 18 bird species (of which 12 were raptors), most commonly with the Buzzard {Buteo buteo). Such interactions declined during the course of the season. Prey pro visioning to nestlings was greatest in the morning and late in the afternoon declining in the intermediate period. Key words: Buteo rufinus, reproduction, behaviour, Greece. Addresses: Zaliki 4, GR-115 24 Athens, Greece (H. A.); Department of Zoology, Aristotelian University of Thessaloniki, GR-54006, Thessaloniki, Macedonia, Greece (V. G.); Laboratory of Ecology and Environmental Sciences, Agricultural University of Athens 75 Iera Odos 1 1855 Athens, Greece (M. G. K.). 1. Introduction The Long-legged Buzzard (Buteo rufinus) is a little known raptor of Europe. -
Regional Specialties Western
REGIONAL SPECIALTIES WESTERN OSPREY 21 - 26” length SOUTHERN . FERRUGINOUS . Eagle sized; clean, white body. HAWK Black wrist marks. 20 - 26” length . Glides with kink (M) in long, narrow wings. MISSISSIPPI . Largest buteo; eagle-like. KITE . Pale below with dark leggings. 13 - 15” length . Mostly white tail; 3 color morphs. Long, pointed wings; slim body. Light body; dark wings; narrow, black tail. Not to scale. Buoyant, acrobatic flight. NORTHERN HARRIER 16 - 20” length PRAIRIE FALCON 14 - 18” length . Long, narrow wings and tail; sharp dihedral. Size of Peregrine; much paler plumage. Brown above, streaked brown below – female. Narrow moustache; spotted breast; long tail. Gray above, pale below with black wing tips – male. Dark armpits and partial wing linings. WING PROFILE IMMATURE BALD EAGLE BALD EAGLE GOLDEN EAGLE . Immature birds vary GOLDEN EAGLE greatly in the amount 27 to 35” length of white spotting on body and wings. White showing on wing linings is surely a Bald Eagle. BALD EAGLE . Like large buteo, curvy wings. Head protrudes much less than tail. Slight dihedral to wing profile. NOTE: Some hawks soar and glide with their wings raised above the horizontal, called a dihedral. 27 to 35” length . Head and tail length similar. Long, flat wings. Straight leading edge to wings. 24 to 28” length This guide developed by Paul Carrier is the property of the Hawk Migration Association of North America (HMANA). HMANA is TURKey VUltUre a membership-based, non-profit organization committed to the . Dark wing linings with light flight feathers. conservation of raptors through the scientific study, enjoyment, and . Small head; long tail; sharp dihedral. -
The Use of Green Plant Material in Bird Nests to Avoid Ectoparasites
July1984] ShortCommunications 615 the Spot-wingedFalconet may not benefitthe Monk HoY, G. 1980. Notas nidobio16gicasdel noroestear- Parakeet in such a manner. gentino. II. Physis (Buenos Aires), Secc. C, 39 We are grateful to A. G6mez Dur&n and J. C. Vera (96): 63-66. (INTA) for grantingus the useof the fieldwork areas, MACLEAN,G.L. 1973. The SociableWeaver, part 4: to N. Arguello and M. Nores for their assistancein predators, parasites and symbionts. Ostrich 44: the identification of food remains, and to J. Navarro 241-253. for his help in the field. This work wassupported by STRANECK,R., & G. VASINA. 1982. Unusual behav- a grant from the Subsecretariade Ciencia y Tecno- iour of the Spot-winged Falconet (Spiziapteryx logla (SUBCYT) of Argentina. circumcinctus).Raptor Res. 16: 25-26. LITERATURE CITED Received7 July 1983, accepted21 February1984. DEAN, A. 1971. Notes on Spiziapteryxcircumcinctus. Ibis 113: 101-102. The Use of Green Plant Material in Bird Nests to Avoid Ectoparasites PETER H. WIMBERGER 1 ZoologyDivision, Washington State Museum DB-10, Universityof Washington, Seattle,Washington 98105 USA Certain birds characteristicallyplace green plant causesnestling mortality in and nest desertion by material in their nests.This greenery is not part of birds (Webster 1944, Neff 1945, Fitch et al. 1946, Moss the nest structureproper but is placed haphazardly and Camin 1970, Feare 1976,Wheelwright and Boers- around the edges or inside the nest. The birds re- ma 1979).In general,the increasedmortality due to plenishthe spraysof greenmaterial, often daily, dur- ectoparasitesis causedby the loss of blood, which ing incubation and the nestling period (Brown and weakens the host, by viral disease, or by disease Amadon 1968, Beebe1976, pers.