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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). -
Selection and Use of Nest Sites by Barn Owls in Norfolk, England
j Raptor Res. 28(3):149-153 ¸ 1994 The Raptor ResearchFoundation, Inc. SELECTION AND USE OF NEST SITES BY BARN OWLS IN NORFOLK, ENGLAND PAUL N. JOHNSON The Durrell Instituteof Conservationand Ecology,The University,Canterbury, Kent CT2 7NX United Kingdom AI•STR•CT.--Between1989 and 1993 reproductionwas monitoredat 96 barn owl (Tyro alba) breeding sitesin England. Nestswere locatedin tree cavities,buildings, and nest boxesin farm buildingsand maturetrees. Many of the sitesother than nestboxes used by owls were of human origin, but the number of thosedeclined during the courseof the study due to deteriorationof human-madestructures and competitionfrom otherspecies. Nest boxesincreased the populationdensity from 15 breedingpairs/100 km2 to 27 pairs.Over the studyperiod, pairs usingnest boxes produced significantly larger clutchesthan at other sites,but the numberof fledglingswas not significantlydifferent amongtypes of nest sites. KEY WORDS: barn owl; breedingecology; England; human-altered habitats; nest boxes; Tyro alba. Selecci6ny usode sitiosde nidificaci6npor Tyroalba en Norfolk, Inglaterra RESUMEN.--Entre1989 y 1993 semonitore6 la reproducci6nen 96 sitiosreproductivos de Tyroalba. Los nidosse localizaron en cavidadesde firboles,edificios, cajas anideras en construccionesagricolas y firboles madufos.Mucho de estossitios, aparte de las cajasanideras, usados por T. alba fueron de origen humano, peroel nfimerode ellosdeclin6 durante el cursodel estudiodebido al deteriorode las estructurasartificiales y a la competenciacon otras especies.Las cajasanideras incrementaron la densidadpoblacional de 15 parejasreproductivas/100 km 2 a 27 parejas.En el periodode estudio,las parejasque usaronlas cajas aniderasprodujeron nidadas significativamentemils grandesqueen otros sitios, pero el nfimero de volantonesno fue significativamentediferente entre los distintostipos de sitios. [Traducci6n de Ivan Lazo] The barn owl (Tyro alba) is currentlyclassified box studieshas been criticized by Moller (1989, as vulnerable in northwest Norfolk, England by 1992). -
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). -
Do the Winter Diets of Sympatric Burrowing Owl and Short-Eared Owl Overlap in West-Central Mexico?
Proceedings of the Fourth International Partners in Flight Conference: Tundra to Tropics 96–101 DO THE WINTER DIETS OF SYMPATRIC BURROWING OWL AND SHORT-EARED OWL OVERLAP IN WEST-CENTRAL MEXICO? HÉCTOR E. VALDEZ-GÓMEZ,1,3 GEOFFREY L. HOLROYD,2 HELEN E. TREFRY,2 AND ARMANDO J. CONTRERAS-BALDERAS1 1Laboratorio de Ornitología, Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, Ciudad Universitaria CP 66451, A.P. 425 San Nicolás de los Garza, Nuevo León, México; and 2Environment Canada, Room 200, 4999-98 Avenue, Edmonton, Alberta T6B 2X3, Canada Abstract. Burrowing Owl (Athene cunicularia) and Short-eared Owl (Asio fl ammeus) are widely dis- tributed but uncommon species during winter in Mexico. Information about their winter ecology is limited, particularly in areas where both species are present. Knowledge of their diet is an important component to understand the nocturnal raptors’ habitat requirements. We analyzed 179 pellets of Burrowing Owl and 354 pellets of Short-eared Owl collected in 2002-2003, at the Military Airbase of Zapopan, Jalisco. The owls shared three main prey categories: invertebrates, small mammals, and birds. Small mammals provided the highest proportion of biomass in the Short-eared Owl diet and invertebrates in the Burrowing Owl diet. Food-niche breadth was lower in Short-eared than in Burrowing Owl refl ecting the diversity of invertebrates in the Burrowing Owl’s diet. The dietary overlap included items of relative low mass such as Northern Pigmy Mouse (Baiomys taylori) and the Gray Bird Grasshopper (Schistocerca nitiens). Zapopan Airbase is important for these two species and others adjacent to a large metropolitan city and should be managed as wildlife habitat that is compat- ible with its function for military training. -
Gtr Pnw343.Pdf
Abstract Marcot, Bruce G. 1995. Owls of old forests of the world. Gen. Tech. Rep. PNW- GTR-343. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 64 p. A review of literature on habitat associations of owls of the world revealed that about 83 species of owls among 18 genera are known or suspected to be closely asso- ciated with old forests. Old forest is defined as old-growth or undisturbed forests, typically with dense canopies. The 83 owl species include 70 tropical and 13 tem- perate forms. Specific habitat associations have been studied for only 12 species (7 tropical and 5 temperate), whereas about 71 species (63 tropical and 8 temperate) remain mostly unstudied. Some 26 species (31 percent of all owls known or sus- pected to be associated with old forests in the tropics) are entirely or mostly restricted to tropical islands. Threats to old-forest owls, particularly the island forms, include conversion of old upland forests, use of pesticides, loss of riparian gallery forests, and loss of trees with cavities for nests or roosts. Conservation of old-forest owls should include (1) studies and inventories of habitat associations, particularly for little-studied tropical and insular species; (2) protection of specific, existing temperate and tropical old-forest tracts; and (3) studies to determine if reforestation and vege- tation manipulation can restore or maintain habitat conditions. An appendix describes vocalizations of all species of Strix and the related genus Ciccaba. Keywords: Owls, old growth, old-growth forest, late-successional forests, spotted owl, owl calls, owl conservation, tropical forests, literature review. -
Tc & Forward & Owls-I-IX
USDA Forest Service 1997 General Technical Report NC-190 Biology and Conservation of Owls of the Northern Hemisphere Second International Symposium February 5-9, 1997 Winnipeg, Manitoba, Canada Editors: James R. Duncan, Zoologist, Manitoba Conservation Data Centre Wildlife Branch, Manitoba Department of Natural Resources Box 24, 200 Saulteaux Crescent Winnipeg, MB CANADA R3J 3W3 <[email protected]> David H. Johnson, Wildlife Ecologist Washington Department of Fish and Wildlife 600 Capitol Way North Olympia, WA, USA 98501-1091 <[email protected]> Thomas H. Nicholls, retired formerly Project Leader and Research Plant Pathologist and Wildlife Biologist USDA Forest Service, North Central Forest Experiment Station 1992 Folwell Avenue St. Paul, MN, USA 55108-6148 <[email protected]> I 2nd Owl Symposium SPONSORS: (Listing of all symposium and publication sponsors, e.g., those donating $$) 1987 International Owl Symposium Fund; Jack Israel Schrieber Memorial Trust c/o Zoological Society of Manitoba; Lady Grayl Fund; Manitoba Hydro; Manitoba Natural Resources; Manitoba Naturalists Society; Manitoba Critical Wildlife Habitat Program; Metro Propane Ltd.; Pine Falls Paper Company; Raptor Research Foundation; Raptor Education Group, Inc.; Raptor Research Center of Boise State University, Boise, Idaho; Repap Manitoba; Canadian Wildlife Service, Environment Canada; USDI Bureau of Land Management; USDI Fish and Wildlife Service; USDA Forest Service, including the North Central Forest Experiment Station; Washington Department of Fish and Wildlife; The Wildlife Society - Washington Chapter; Wildlife Habitat Canada; Robert Bateman; Lawrence Blus; Nancy Claflin; Richard Clark; James Duncan; Bob Gehlert; Marge Gibson; Mary Houston; Stuart Houston; Edgar Jones; Katherine McKeever; Robert Nero; Glenn Proudfoot; Catherine Rich; Spencer Sealy; Mark Sobchuk; Tom Sproat; Peter Stacey; and Catherine Thexton. -
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. -
Owls-Of-Nh.Pdf
Lucky owlers may spot the stunning great gray owl – but only in rare years when prey is sparse in its Arctic habitat. ©ALAN BRIERE PHOTO 4 January/February 2009 • WILDLIFE JOURNAL OWLSof NEW HAMPSHIRE Remarkable birds of prey take shelter in our winter woods wls hold a special place in human culture and folklore. The bright yellow and black eyes surrounded by an orange facial disc Oimage of the wise old owl pervades our literature and conjures and a white throat patch. up childhood memories of bedtime stories. Perhaps it’s their circular Like most owls, great horned owls are not big on building their faces and big eyes that promote those anthropomorphic analogies, own nests. They usually claim an old stick nest of another species or maybe it is owls’ generally nocturnal habits that give them an air – perhaps one originally built by a crow, raven or red-tailed hawk. In of mystery and fascination. New Hampshire, great horned owls favor nest- New Hampshire’s woods and swamps are ing in great blue heron nests in beaver-swamp home to several species of owls. Four owl spe- BY IAIN MACLEOD rookeries. Many times, while checking rooker- cies regularly nest here: great horned, barred, ies in early spring, I’ll see the telltale feather Eastern screech and Northern saw-whet. One other species, the tufts sticking up over the edge of a nest right in the middle of all long-eared owl, nests sporadically in the northern part of the state. the herons. Later in the spring, I’ll return and see a big fluffy owlet None of these species is rare enough to be listed in the N.H. -
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. -
Barred Owl (Strix Varia)
Wild Things in Your Woodlands Barred Owl (Strix varia) The barred owl is a large bird, up to 20 inches long, with a wingspan of 44 inches. It is gray-brown in color, with whitish streaks on the back and head, brown horizontal bars on its white chest, and vertical bars on its belly. This owl has a round face without ear tufts, and a whitish facial disk with dark concentric rings around brown eyes. Males and females look similar, but females can weigh about one third more than males. “Who cooks for you, who cooks for you all?” This is the familiar call of the barred owl defending its territory or attracting a mate. If you live in or near a heavily wooded area with mature forest, particularly if there is also a stream or other body of water nearby, this sound is probably familiar. Barred owls are the most vocal of our owls, and most often are heard calling early at night and at dawn. They call year-round, but courtship activities begin in February and breeding takes place primarily in March and April. Nesting in cavities or abandoned hawk, squirrel, or crow nests, the female sits on a nest of 1-5 eggs for 28 to 33 days. During this time, the male brings food to her. Once the eggs have hatched, both parents care for the fledglings for at least 4 months. Barred owls mate for life, reuse their nest site for many years, and maintain territories from 200 – 400 acres in size. Barred owls are strongly territorial and remain in their territories for most, if not all, of the year. -
Barn Owl (Tyto Alba) Caleb G
Barn Owl (Tyto alba) Caleb G. Putnam Status: State Endangered, Casual (MBRC) these reports occurred during MBBA II, two one-day wonders at Tawas Point State Park, Iosco County, were clearly migrants and may have pertained to the same individual. The third, present for two days in July 2002 in Washtenaw County, yielded possible breeding evidence. This compares to one breeding confirmation and five non-breeding season observations during MBBA I. After the MBBA II period, a single Barn Owl was observed in and near a barn on 7 September 2009 in Penn Township, Cass County and several dropped feathers were retrieved (MBRC 2010, Putnam 2010). Still, it seems likely that the period between the two Tawas Point, Iosco County, MI. 5/17/2007 atlases witnessed the conclusion of this species’ © Caleb Putnam regular breeding in the state. The monkey-faced Barn Owl has the dubious Historically, breeding activity occurred distinction of being one of Michigan’s few primarily from March to June, with occasional extirpated breeding bird species. Formerly an records into October during times of high uncommon to rare breeder in the southern LP, microtine abundance. The species shows a the species last nested in the early 1980s and has marked preference for human-made nest since been only infrequently encountered. This structures, in which a clutch of 3-11 eggs is laid. species is one of the most widely distributed of Eggs are incubated for about 30-34 days and the all land birds, being found on six continents and young are brooded an additional 52-56 days constituting approximately 28 to 35 subspecies (Ehrlich et al. -
Birds of Prey (Accipitriformes and Falconiformes) of Serra De Itabaiana National Park, Northeastern Brazil
Acta Brasiliensis 4(3): 156-160, 2020 Original Article http://revistas.ufcg.edu.br/ActaBra http://dx.doi.org/10.22571/2526-4338416 Birds of prey (Accipitriformes and Falconiformes) of Serra de Itabaiana National Park, Northeastern Brazil Cleverton da Silvaa* i , Cristiano Schetini de Azevedob i , Juan Ruiz-Esparzac i , Adauto de Souza d i Ribeiro h a Programa de Pós-Graduação em Desenvolvimento e Meio Ambiente, Universidade Federal de Sergipe, Aracajú, São Cristóvão, 49100-100, Sergipe, Brasil. *[email protected] b Programa de Pós-Graduação em Ecologia de Biomas Tropicais, Universidade Federal de Ouro Preto, Ouro Preto, 35400-000, Minas Gerais, Brasil. c Universidade Federal de Sergipe, Nossa Senhora da Glória, 49680-000, Sergipe, Brasil. d Universidade Federal de Sergipe, Aracajú, São Cristóvão, 49100-100, Sergipe, Brasil. Received: June 20, 2020 / Accepted: August 27, 2020/ Published online: September 28, 2020 Abstract Birds of prey are important for maintaining ecosystems, since they can regulate the populations of vertebrates and invertebrates. However, anthropic activities, like habitat fragmentation, have been decreasing the number of birds of prey, affecting the habitat ecological relations and, decreasing biodiversity. Our objective was to evaluate species of birds of prey (Accipitriformes and Falconiformes) in a protected area of the Atlantic forest in northeastern Brazil. The area was sampled for 17 months using fixed points and walking along a pre-existing trail. Birds of prey were classified by their Punctual Abundance Index, threat status and forest dependence. Sixteen birds of prey were recorded, being the most common Rupornis magnirostris and Caracara plancus. Most species were considered rare in the area and not dependent of forest vegetation.