Identification of Bald and Golden Eagle Feathers
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Spatial Relationships of Nesting Golden Eagles in Central Utah
White, C. M. 1974. The 1974 raptor surveyof the AlaskaPipeline between Franklin Bluffsand Big Delta. Unpubl.interim rep. to U.S.Fish and Wildl. Serv.,Anchorage, AK. 10 pp. White, C. M., T. D. Ray,and L. W. Sowl.1977. The 1970-1972-1974raptor surveys alongthe Trans-AlaskaOil Pipeline.pp. 199-221.In.' Chancellor,R.D. (ed.).World Conferenceon Birdsof Prey, Reportof the Proceedings.International Council for BirdPreservation. 440 pp. + appendices. SPATIAL RELATIONSHIPS OF NESTING GOLDEN EAGLES IN CENTRAL UTAH by DwightG. Smith• BiologyDepartment SouthernConnecticut State University New Haven, Connecticut 06515 and JosephR. Murphy Departmentof Zoology BrighamYoung University Provo, Utah 84602 Abstract We examinedthe distributionof GoldenEagle (Aquila chrysaetos)nest sites in the easternGreat Basinusing the Clark-Evansnearest-neighbor method of analysis.Distri- butionvalues indicated. uniform spacing of nestsites within the hills and ridges,which providedall of the potentialnesting sites in the studyarea. Analysis of GoldenEagle nestsite distributionwith three other large raptorssuggested a tendencytoward uni- form spacingbetween diurnal raptor speciesand aggregationwith the Great Horned Owl (Bubovirginianus). Introduction Odum(1971) suggested that populationsexhibit one of threedistribution patterns: (1) random,where habitat is homogenousand individualsdo not normallyinteract; (2) uni- form,where habitat is homogenousand individualscompete for one or moreresources; (3) aggregated,that mayresult from either heterogenous habitat or a tendencyto aggre- gatesocially. Newton (1979) noted that manyspecies exhibit uniform distribution of ter- ritoriesand nest sites except where available sites are limitedand concentrated,such as in the SnakeRiver Birds of PreyNatural Area. Our observationsof GoldenEagles in the easternGreat BasinDesert revealed a concentrationof nestsites in high, north-south orientedridges and hills but nonein interveningbroad, flat valleys.Herein we examine thisdistribution using the Clark-Evansnearest-neighbor model (1954). -
Bald Eagle Haliaetus Leucocephalus
Appendix A: Birds Bald Eagle Haliaetus leucocephalus Federal Listing N/A State Listing T Global Rank G4 State Rank S2 Regional Status Photo by Jason Lambert Justification (Reason for Concern in NH) Bald Eagle populations in the conterminous United States entered a severe population decline in the 1950s, largely a result of reproductive failure induced by biomagnification of the insecticide DDT (Buehler 2000). Some regional breeding populations, especially in eastern and southern states, became locally extirpated. This serious decline led to the designation of the bald eagle as Endangered under the Endangered Species Act. Following the banning of DDT and intensive reintroduction efforts, Bald Eagle populations gradually rebounded, and the species was removed from the federal endangered list in 2007. In the Northeast, recovery has been particularly strong since 2000. However, most states still consider Bald Eagle a SGCN due to historic extirpations and historic sensitivity to certain environmental stressors, particularly contaminants. Distribution Bald eagles currently occur and breed in all Lower 48 states and in Alaska. Based upon data provided by state agencies, from a population low of 417 breeding pairs in 1963 the U.S. Fish and Wildlife Service estimated that there were an estimated 1,500 breeding pairs in the contiguous 48 states in 1982 and an estimated 5,300 pairs in the same area in 1997 (derived from data in Buehler 2000), and nearly 9800 breeding pairs in the Lower 48 states in 2006. The USFWS estimated that there were 463 breeding pairs in the six New England states in 2006. The nationwide population has probably increased substantially since 2006, but more recently compiled information is not available from USFWS. -
Bird Report 1999
YELLOWSTONE BIRD REPORT 1999 Terry McEneaney Yellowstone Center for Resources National Park Service Yellowstone National Park, Wyoming YCR–NR–2000–02 Suggested citation: McEneaney, T. 2000. Yellowstone Bird Report, 1999. National Park Service, Yellowstone Center for Resources, Yellowstone National Park, Wyoming, YCR–NR–2000–02. Cover: Special thanks to my wife, Karen McEneaney, for the stunning pencil drawing of a Golden Eagle (Aquila chrysaetos) talon. The Golden Eagle is one of Yellowstone’s most formidable avian predators. When viewing Golden Eagle talons up close, one soon realizes why the bird is a force to be reckoned with in the natural world. Title page: Great Horned Owlet. The photographs in this report are courtesy of Terry McEneaney. ii CONTENTS INTRODUCTION ..................................................................... 5 Bird Impression .............................................................. 20 Weather Patterns and Summary ....................................... 5 National Geographic Field Guide .................................... 21 THREATENED AND ENDANGERED SPECIES .............................. 7 Retirement of Yellowstone Pilot Dave Stradley .............. 21 Peregrine Falcon ............................................................... 7 Yellowstone Birds: Their Ecology and Distribution ....... 21 Bald Eagle ........................................................................ 7 Computerized Database ................................................. 21 Whooping Crane ............................................................. -
Air Speeds of Migrating Birds Observed by Ornithodolite and Compared with Predictions from Flight Theory Rsif.Royalsocietypublishing.Org C
Air speeds of migrating birds observed by ornithodolite and compared with predictions from flight theory rsif.royalsocietypublishing.org C. J. Pennycuick1, Susanne A˚kesson2 and Anders Hedenstro¨m2 1School of Biological Sciences, University of Bristol, Bristol BS8 1UG, UK 2Department of Biology, Centre for Animal Movement Research, Lund University, Ecology Building, 223 62 Lund, Sweden Research We measured the air speeds of 31 bird species, for which we had body mass Cite this article: Pennycuick CJ, A˚kesson S, and wing measurements, migrating along the east coast of Sweden in Hedenstro¨m A. 2013 Air speeds of migrating autumn, using a Vectronix Vector 21 ornithodolite and a Gill WindSonic anem- ometer. We expected each species’ average air speed to exceed its calculated birds observed by ornithodolite and compared minimum-power speed (Vmp), and to fall below its maximum-range speed with predictions from flight theory. J R Soc (Vmr), but found some exceptions to both limits. To resolve these discrepancies, Interface 10: 20130419. we first reduced the assumed induced power factor for all species from 1.2 to http://dx.doi.org/10.1098/rsif.2013.0419 0.9, attributing this to splayed and up-turned primary feathers, and then assigned body drag coefficients for different species down to 0.060 for small waders, and up to 0.12 for the mute swan, in the Reynolds number range 25 000–250 000. These results will be used to amend the default values in exist- Received: 8 May 2013 ing software that estimates fuel consumption in migration, energy heights on Accepted: 31 May 2013 arrival and other aspects of flight performance, using classical aeronautical theory. -
A Multi-Gene Phylogeny of Aquiline Eagles (Aves: Accipitriformes) Reveals Extensive Paraphyly at the Genus Level
Available online at www.sciencedirect.com MOLECULAR SCIENCE•NCE /W\/Q^DIRI DIRECT® PHYLOGENETICS AND EVOLUTION ELSEVIER Molecular Phylogenetics and Evolution 35 (2005) 147-164 www.elsevier.com/locate/ympev A multi-gene phylogeny of aquiline eagles (Aves: Accipitriformes) reveals extensive paraphyly at the genus level Andreas J. Helbig'^*, Annett Kocum'^, Ingrid Seibold^, Michael J. Braun^ '^ Institute of Zoology, University of Greifswald, Vogelwarte Hiddensee, D-18565 Kloster, Germany Department of Zoology, National Museum of Natural History, Smithsonian Institution, 4210 Silver Hill Rd., Suitland, MD 20746, USA Received 19 March 2004; revised 21 September 2004 Available online 24 December 2004 Abstract The phylogeny of the tribe Aquilini (eagles with fully feathered tarsi) was investigated using 4.2 kb of DNA sequence of one mito- chondrial (cyt b) and three nuclear loci (RAG-1 coding region, LDH intron 3, and adenylate-kinase intron 5). Phylogenetic signal was highly congruent and complementary between mtDNA and nuclear genes. In addition to single-nucleotide variation, shared deletions in nuclear introns supported one basal and two peripheral clades within the Aquilini. Monophyly of the Aquilini relative to other birds of prey was confirmed. However, all polytypic genera within the tribe, Spizaetus, Aquila, Hieraaetus, turned out to be non-monophyletic. Old World Spizaetus and Stephanoaetus together appear to be the sister group of the rest of the Aquilini. Spiza- stur melanoleucus and Oroaetus isidori axe nested among the New World Spizaetus species and should be merged with that genus. The Old World 'Spizaetus' species should be assigned to the genus Nisaetus (Hodgson, 1836). The sister species of the two spotted eagles (Aquila clanga and Aquila pomarina) is the African Long-crested Eagle (Lophaetus occipitalis). -
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. -
Free Download! the Trumpeter Swan
G3647 The Trumpeter Swan by Sumner Matteson, Scott Craven and Donna Compton Snow-white Trumpeter Swans present a truly spectac- Swans of the Midwest ular sight. With a wingspan of more than 7 feet and a rumpeter Swans, along with ducks and geese, belong height of about 4 feet, the Trumpeter Swan (Cygnus buc- to the avian Order Anseriformes, Family Anatidae. cinator) ranks as the largest native waterfowl species in T Trumpeters have broad, flat bills with fine tooth-like North America. serrations along the edges which allow them to strain Because the Trumpeter Swan disappeared as a breed- aquatic plants and water. The birds’ long necks and ing bird in the Midwest, several states have launched strong feet allow them to uproot plants in water up to 4 restoration programs to reintroduce it to the region. This feet deep. publication will provide you with background informa- Most Trumpeter Swans weigh 21–30 pounds, tion on the Trumpeter Swan’s status and life history, and although some males exceed the average weight. The on restoration efforts being conducted in the upper male is called a cob; the female is called a pen; and a swan Midwest. in its first year is called a cygnet or juve- nile. The Trumpeter is often con- fused with the far more common Tundra Swan (formerly Whistling Swan, Cygnus columbianus), the only other native swan found routinely in North America. Tundra Swans can be seen in the upper Trumpeter Swan Midwest only during spring and fall migration. You can distinguish between the two native species most accurately by listening to their calls. -
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. -
Bald Eagle Haliaeetus Leucocephalus
Wyoming Species Account Bald Eagle Haliaeetus leucocephalus REGULATORY STATUS USFWS: Delisted; Migratory Bird USFS R2: Sensitive USFS R4: Sensitive Wyoming BLM: Sensitive State of Wyoming: Protected Bird CONSERVATION RANKS USFWS: Bird of Conservation Concern WGFD: NSS3 (Bb), Tier II WYNDD: G5, S4B/S5N Wyoming Contribution: LOW IUCN: Least Concern PIF Continental Concern Score: 9 STATUS AND RANK COMMENTS Bald Eagle (Haliaeetus leucocephalus) is provided international protection under the Federal Migratory Bird Treaty Act of 1918, as amended 1. In 1940, Bald Eagle was provided protection under the Bald and Golden Eagle Protection Act 2. In 1966, the southern subspecies was listed as federally endangered under the Endangered Species Preservation Act; the entire population in the contiguous United States was listed as endangered in 1978 under the 1973 Endangered Species Act (ESA). A significant increase in numbers of nesting pairs, productivity, and distribution allowed Bald Eagle to be reclassified from Endangered to Threatened in 1995 under the ESA 3. Bald Eagle was delisted in 2007, and numbers are considered to be stable to increasing across its range 4. The species has been assigned different state conservation ranks by the Wyoming Natural Diversity Database for the breeding season and nonbreeding season because the abundance of the species is different between seasons. NATURAL HISTORY Taxonomy: Bald Eagle is a member of the family Accipitridae, which includes kites, eagles, harriers, and hawks 5. There are two subspecies of Bald Eagle; H. l. alascanus is found north of 40 degrees latitude across North America, including Wyoming, while H. l. leucocephalus is found south of 40 degrees latitude in the Gulf coast states 6. -
Arctic National Wildlife Refuge
FACT SHEET Arctic National Wildlife Refuge ARCTIC BIRDS IN YOUR STATE The Arctic National Wildlife Refuge is a place unlike any Alabama - Ruby-crowned Kinglet Alaska - Redpoll other in the world. The Alaskan refuge, often referred to Arizona - Fox Sparrow as “America’s Serengeti,” is a remote sanctuary for diverse Arkansas - Mallard California - Snow Goose populations of migratory birds, fish, mammals, and marine Colorado - Bohemian Waxwing Connecticut - Greater Scaup life. The Refuge spans an area roughly the size of South Delaware - Black-bellied Plover Carolina and boasts snow-capped mountains, arctic tundra, Florida - Peregrine Falcon Georgia - Gray-checked Thrush foothills, wetlands, boreal forest, and fragile coastal plains. Hawaii - Wandering Tattler America’s Arctic Refuge was set aside as a safe haven for Idaho - Short-eared Owl Illinois - Northern Flicker wildlife in 1960, and it has remained wild in its more than Indiana - Dark-eyed Junco 50 years as a Refuge. Iowa - Sharp-shinned Hawk Kansas - Smith’s Longspur Kentucky – Merlin AMERICA’S LAST GREAT WILDERNESS Louisiana - Long-billed Dowitcher Maine - Least Sandpiper Maryland - Tundra Swan The Arctic Refuge is often mischaracterized as a blank, frozen void Massachusetts - Golden Plover of uninhabited tundra. Although winter frequently coats the Arc- Michigan - Long-tail Duck tic with snow and freezes the ground, it gives way to lush, vibrant Minnesota - Snowy Owl Mississippi – Northern Waterthrush growth in warmer months. In fact, the Refuge’s unparalleled diver- Missouri - American Pipit sity makes it the most biologically productive habitat in the North. Montana - Golden Eagle Nebraska - Wilson’s Warbler Landscape Nevada - Green-winged Teal The majestic Brooks Range rises 9,000 feet, providing sharp contrast New Hampshire - Dunlin New Jersey – Canvasback to the flat, wetlands-rich coastal plains at its feet. -
Ecoregions of the Mississippi Alluvial Plain
92° 91° 90° 89° 88° Ecoregions of the Mississippi Alluvial Plain Cape Girardeau 73cc 72 io Ri Ecoregions denote areas of general similarity in ecosystems and in the type, quality, and quantity of This level III and IV ecoregion map was compiled at a scale of 1:250,000 and depicts revisions and Literature Cited: PRINCIPAL AUTHORS: Shannen S. Chapman (Dynamac Corporation), Oh ver environmental resources; they are designed to serve as a spatial framework for the research, subdivisions of earlier level III ecoregions that were originally compiled at a smaller scale (USEPA Bailey, R.G., Avers, P.E., King, T., and McNab, W.H., eds., 1994, Omernik, J.M., 1987, Ecoregions of the conterminous United States (map Barbara A. Kleiss (USACE, ERDC -Waterways Experiment Station), James M. ILLINOIS assessment, management, and monitoring of ecosystems and ecosystem components. By recognizing 2003, Omernik, 1987). This poster is part of a collaborative effort primarily between USEPA Region Ecoregions and subregions of the United States (map) (supplementary supplement): Annals of the Association of American Geographers, v. 77, no. 1, Omernik, (USEPA, retired), Thomas L. Foti (Arkansas Natural Heritage p. 118-125, scale 1:7,500,000. 71 the spatial differences in the capacities and potentials of ecosystems, ecoregions stratify the VII, USEPA National Health and Environmental Effects Research Laboratory (Corvallis, Oregon), table of map unit descriptions compiled and edited by McNab, W.H., and Commission), and Elizabeth O. Murray (Arkansas Multi-Agency Wetland Bailey, R.G.): Washington, D.C., U.S. Department of Agriculture - Forest Planning Team). 37° environment by its probable response to disturbance (Bryce and others, 1999). -
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.