Falco Rusticolus
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Gyrfalcon Falco Rusticolus
Gyrfalcon Falco rusticolus Rob Florkiewicz surveys, this area was included. Eight eyries are known from this Characteristics and Range The northern-dwelling Gyrfalcon is part of the province; however, while up to 7 of these eyries have the largest falcon in the world. It breeds mostly along the Arctic been deemed occupied in a single year, no more than 3 have been coasts of North America, Europe and Asia (Booms et al. 2008). productive at the same time. Based on these data and other Over its range, its colour varies from white through silver-grey to sightings, the British Columbia Wildlife Branch estimates the almost black; silver-grey is the most common morph in British breeding population in the province to be fewer than 20 pairs Columbia. It nests on cliff ledges at sites that are often used for (Chutter 2008). decades and where considerable amounts of guano can accumulate. Ptarmigan provide the Gyrfalcon's main prey in In British Columbia, the Gyrfalcon nests on cliff ledges on British Columbia and productivity appears dependent on mountains in alpine areas, usually adjacent to rivers or lakes. ptarmigan numbers. Large size and hunting prowess make the Occasionally, it nests on cliffs of river banks and in abandoned Gyrfalcon a popular bird with falconers, who breed and train Golden Eagle nests. them to hunt waterfowl and other game birds. Conservation and Recommendations Whilst the Gyrfalcon is Distribution, Abundance, and Habitat Most Gyrfalcons breed designated as Not at Risk nationally by COSEWIC, it is Blue-listed along the Arctic coast; however, a few breed in the northwest in British Columbia due to its small known breeding population portion of the Northern Boreal Mountains Ecoprovince of British (British Columbia Ministry of Environment 2014). -
Life History Account for Peregrine Falcon
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group PEREGRINE FALCON Falco peregrinus Family: FALCONIDAE Order: FALCONIFORMES Class: AVES B129 Written by: C. Polite, J. Pratt Reviewed by: L. Kiff Edited by: L. Kiff DISTRIBUTION, ABUNDANCE, AND SEASONALITY Very uncommon breeding resident, and uncommon as a migrant. Active nesting sites are known along the coast north of Santa Barbara, in the Sierra Nevada, and in other mountains of northern California. In winter, found inland throughout the Central Valley, and occasionally on the Channel Islands. Migrants occur along the coast, and in the western Sierra Nevada in spring and fall. Breeds mostly in woodland, forest, and coastal habitats. Riparian areas and coastal and inland wetlands are important habitats yearlong, especially in nonbreeding seasons. Population has declined drastically in recent years (Thelander 1975,1976); 39 breeding pairs were known in California in 1981 (Monk 1981). Decline associated mostly with DDE contamination. Coastal population apparently reproducing poorly, perhaps because of heavier DDE load received from migrant prey. The State has established 2 ecological reserves to protect nesting sites. A captive rearing program has been established to augment the wild population, and numbers are increasing (Monk 1981). SPECIFIC HABITAT REQUIREMENTS Feeding: Swoops from flight onto flying prey, chases in flight, rarely hunts from a perch. Takes a variety of birds up to ducks in size; occasionally takes mammals, insects, and fish. In Utah, Porter and White (1973) reported that 19 nests averaged 5.3 km (3.3 mi) from the nearest foraging marsh, and 12.2 km (7.6 mi) from the nearest marsh over 130 ha (320 ac) in area. -
Natural History of the Gyrfalcon in the Central Canadian Arctic K.G
ARCTIC VOL. 41, NO. 1 (MARCH 1988) P. 31-38 Natural History of the Gyrfalcon in the Central Canadian Arctic K.G. POOLE' and R.G. BROMLEY2 (Received 24 March 1987; accepted in revised form 24 September 1987) ABSTRACT. A population of breeding gyrfalcons was studied from 1982to 1986 on 2000a km2 area in thecentral Arctic of the NorthwestTerritories. Each year 14-18 territories were occupied. The meanintemest distance was 10.6 km, giving oneof the highest recorded densitiesfor the species. There was a tendency for regularity in spacing of territories. Most (85%) nests were in abandoned stick nests of common ravens or golden eagles. Rough-legged hawk nests were not used by gyrfalcons, despite numerous available.date Mean of initiation of laying was 8 May. Meansize of clutch was 3.80 and of brood was 2.53, and mean productivity was 1SO fledged young. A reduction of 48% from estimated numberof eggs laid to number of fledglings was determined. Reproductive success declined with increased severity of spring weather, notablydays increased and amount of precipitation. Key words: gyrfalcon (Falco rusticolus),natural history, reproductive ecology, central Arctic RÉSUMÉ. Qtre 1982 et 1986, on a étudié une populationde gerfauts en reproduction dans une zone de 2000 km2dans la région centrale arctiquedes Territoires du Nord-Ouest. Quatorze des 18 aires étaient occupées chaque année. La distance entremoyenne les nids étaitde 10,6km, soit la plus grande densité relevée pour cetteespèce. Les aires avaient tendanceB être espacéesrégulitrement. La plupart des nids(85 p. cent) étaient situésdans des nids de brindilles occupés précédemment pardes corbeaux communsou des aigles dorés. -
Falco Peregrinus Tunstall Peregrineperegrine Falcon,Falcon Page 1
Falco peregrinus Tunstall peregrineperegrine falcon,falcon Page 1 State Distribution Best Survey Period Copyright: Rick Baetsen Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Status: State Endangered Dakota, Florida, Oklahoma, Arkansas, Alabama, Mississippi, Louisiana, Texas, and Nevada. In Mexico, Global and state rank: G4/S1 peregrine falcon is present on the Baja Peninsula, islands of the Gulf of California, and northwestern Family: Falconidae – Falcons states of the mainland. Breeding also confirmed for eastern Cuba and the Dominican Republic (White et al. Total range: While having one of the most extensive 2002). global distributions, peregrine falcons were never abundant anywhere, due to its specific habitat State distribution: Barrows (1912) noted that the requirements and position in the food web as a top peregrine falcon was “nowhere common” and Wood predator (Hess 1991). The species was formerly (1951) called the species a rare local summer resident extirpated throughout much of its original range due to in northern counties along the Great Lakes. Isaacs exposure to organic chemicals such as DDT, and (1976) described ten historical nesting sites in Michigan: reoccupancy and restoration is still incomplete (White et Goose Lake escarpments, Huron Islands, Huron al. 2002). Three subspecies occur in North America, Mountains, and Lake Michigamme in Marquette with F. p. anatum being the subspecies that breeds in County; Grand Island and Pictured Rocks in Alger Michigan. Payne (1983) noted that F. p. tundrius is an County; Garden Peninsula of Delta County; Isle Royale occasional transient in the State. See White et al. in Keweenaw County; Mackinac Island in Mackinac (2002) and citations therein for a detailed description of County; and South Fox Island in Leelanau County. -
Syringeal Morphology and the Phylogeny of the Falconidae’
The Condor 96:127-140 Q The Cooper Ornithological Society 1994 SYRINGEAL MORPHOLOGY AND THE PHYLOGENY OF THE FALCONIDAE’ CAROLES.GRIFFITHS Departmentof Ornithology,American Museum of NaturalHistory and Departmentef Biology, City Collegeof City Universityof New York, Central Park West at 79th St., New York, NY 10024 Abstract. Variation in syringealmorphology was studied to resolve the relationshipsof representativesof all of the recognized genera of falcons, falconets, pygmy falcons, and caracarasin the family Falconidae. The phylogenyderived from thesedata establishesthree major cladeswithin the family: (1) the Polyborinae, containingDaptrius, Polyborus, Milvago and Phalcoboenus,the four genera of caracaras;(2) the Falconinae, consistingof the genus Falco, Polihierax (pygmy falcons),Spiziapteryx and Microhierax (falconets)and Herpetothe- res (Laughing Falcon); and (3) the genus Micrastur(forest falcons) comprising the third, basal clade. Two genera, Daptriusand Polihierax,are found to be polyphyletic. The phy- logeny inferred from these syringealdata do not support the current division of the family into two subfamilies. Key words: Falconidae;phylogeny; systematics; syrinx; falcons; caracaras. INTRODUCTION 1. The Polyborinae. This includes seven gen- Phylogenetic relationships form the basis for re- era: Daptrius, Milvago, Polyborus and Phalco- searchin comparative and evolutionary biology boenus(the caracaras),Micrastur (forest falcons), (Page1 and Harvey 1988, Gittleman and Luh Herpetotheres(Laughing Falcon) and Spiziapter- 1992). Patterns drawn from cladogramsprovide yx (Spot-winged Falconet). the blueprints for understanding biodiversity, 2. The Falconinae. This includes three genera: biogeography,behavior, and parasite-hostcospe- Falco, Polihierax (pygmy falcons) and Micro- ciation (Vane-Wright et al. 199 1, Mayden 1988, hierax (falconets). Page 1988, Coddington 1988) and are one of the Inclusion of the caracarasin the Polyborinae key ingredients for planning conservation strat- is not questioned (Sharpe 1874, Swann 1922, egies(Erwin 199 1, May 1990). -
Peregrine Falcon Falco Peregrinus Kingdom: Animalia FEATURES Phylum: Chordata the Peregrine Falcon Is Also Known As the Duck Class: Aves Hawk
peregrine falcon Falco peregrinus Kingdom: Animalia FEATURES Phylum: Chordata The peregrine falcon is also known as the duck Class: Aves hawk. It averages 15 to 20 inches in length (tail tip to Order: Falconiformes bill tip in preserved specimen). Like all falcons, it has pointed wings, a thin tail and a quick, flapping Family: Falconidae motion in flight. The peregrine’s dark “sideburns” ILLINOIS STATUS are distinctive. The adult has a blue-gray back, while the chest and belly are white to orange with darker common, native spots and bars. The immature falcon has the same head and facial patterns as the adult but is brown on the upper side. The lower side of the immature bird is cream-colored with brown streaks. BEHAVIORS The peregrine falcon is a migrant, winter resident and summer resident in Illinois. It was extirpated from the state, reintroduced and populations have recovered. The peregrine falcon lives in open areas, like prairies, along Lake Michigan and around other rivers and lakes, especially if large flocks of shorebirds and waterfowl are present. It has also been introduced to cities. Spring migrants begin arriving in March. These birds previously nested in adult Illinois on cliffs and in hollow trees but now may nest on ledges or roofs of tall buildings or bridge © Chris Young, Wildlife CPR structures in urban areas. Three or four, white eggs with dark markings are deposited by the female, and she incubates them for the entire 33- to 35-day, incubation period. Fall migrants begin arriving in Illinois in August. This bird winters as far south as the southern tip of South America. -
WBRC Review List 2020
Official Washington State Checklist of Birds (updated by Washington Bird Records Committee, Nov 2020) __Fulvous Whistling-Duck (1905) __White-throated Swift __Long-tailed Jaeger __Nazca Booby __Tropical Kingbird __Dusky Thrush (s) __Tricolored Blackbird __Emperor Goose __Ruby-throated Hummingbird __Common Murre __Blue-footed Booby __Western Kingbird __Redwing __Brown-headed Cowbird __Snow Goose __Black-chinned Hummingbird __Thick-billed Murre __Brown Booby __Eastern Kingbird __American Robin __Rusty Blackbird __Ross’s Goose __Anna’s Hummingbird __Pigeon Guillemot __Red-footed Booby __Scissor-tailed Flycatcher __Varied Thrush __Brewer’s Blackbird __Gr. White-fronted Goose __Costa’s Hummingbird __Long-billed Murrelet __Brandt’s Cormorant __Fork-tailed Flycatcher __Gray Catbird __Common Grackle __Taiga Bean-Goose __Calliope Hummingbird __Marbled Murrelet __Pelagic Cormorant __Olive-sided Flycatcher __Brown Thrasher __Great-tailed Grackle __Brant __Rufous Hummingbird __Kittlitz’s Murrelet __Double-crested Cormorant __Greater Pewee (s) __Sage Thrasher __Ovenbird __Cackling Goose __Allen’s Hummingbird (1894) __Scripps’s Murrelet __American White Pelican __Western Wood-Pewee __Northern Mockingbird __Northern Waterthrush __Canada Goose __Broad-tailed Hummingbird __Guadalupe Murrelet __Brown Pelican __Eastern Wood-Pewee __European Starling (I) __Golden-winged Warbler __Trumpeter Swan __Broad-billed Hummingbird __Ancient Murrelet __American Bittern __Yellow-bellied Flycatcher __Bohemian Waxwing __Blue-winged Warbler __Tundra Swan __Virginia Rail -
Falco Columbarius Linnaeus Merlin,Merlin Page 1
Falco columbarius Linnaeus Merlin,merlin Page 1 State Distribution Best Survey Period Photo by: Charles W. Cook Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Status: State threatened Schoolcraft) and two northern lower Peninsula counties (Alpena, Antrim). The highest density of nesting merlins Global and state ranks: G5/S1S2 occurs on Isle Royale. Pairs are also sighted annually in the Porcupine Mountains State Park, Ontonagon County, Family: Falconidae (falcons) and in the Huron Mountains, Marquette County. During migration, merlins can be spotted throughout the state. Total Range: Found throughout the northern hemi- sphere, Falco columbarius, in North America occurs in Recognition: The merlin is a medium-sized falcon, the boreal forests of Alaska and Canada south to the about the size of a blue jay, characterized by long, extreme northern portions of the United States, from the pointed wings and rapid wing-beats; a long, heavily Rockies to Maine (Johnsgard 1990). The paler subspe- barred tail; vertically streaked underparts; and faint cies, F. c. richardsoni, breeds in the prairie parklands of “sideburns.” In flight, merlins appear similar to Ameri- central Canada and the darker subspecies F. c. can kestrels (F. sparverius) but lack any brown tones suckleyi, breeds in the Pacific coastal regions. The above or extensive buffy to white underparts (Johnsgard more widespread F. c. columbarius, occupies the 1990). The dark tail with 2-5 highly contrasting remaining range. The merlin winters from the Gulf of narrow light bands helps distinguish the merlin from Mexico to northern South America. the larger peregrine falcon (F. peregrinus) (Sodhi et al. -
1/9/2015 1 G Phylum Chordata Characteristics – May Be With
1/9/2015 Vertebrate Evolution Z Phylum Chordata characteristics – may be with organism its entire life or only during a certain developmental stage 1. Dorsal, hollow nerve cord 2. Flexible supportive rod (notochord) running along dorsum just ventral to nerve cord 3. Pharyngeal slits or pouches 4. A tail at some point in development Z Phylum Chordata has 3 subphyla W Urochordata – tunicates Z Adults are sessile marine animals with gill slits Z Larvae are free-swimming and possess notochord and nerve cord in muscular tail Z Tail is reabsorbed when larvae transforms into an adult 1 1 1/9/2015 W Cephalochordata –lancelets Z Small marine animals that live in sand in shallow water Z Retains gill slits, notochord, and nerve cord thru life W Vertebrata – chordates with a “backbone” Z Persistent notochord, or vertebral column of bone or cartilage Z All possess a cranium Z All embryos pass thru a stage when pharyngeal pouches are present Lamprey ammocoete 2 2 1/9/2015 Jawless Fish Hagfish Lamprey Vertebrate Evolution 1. Tunicate larvae 2. Lancelet 3. Larval lamprey (ammocoete) and jawless fishes 4. Jaw development from anterior pharyngeal arches – capture and ingestion of more food sources 5. Paired fin evolution A. Eventually leads to tetrapod limbs B. Fin spine theory – spiny sharks (acanthodians) had up to 7 pairs of spines along trunk and these may have led to front and rear paired fins 3 3 1/9/2015 Z Emergence onto land W Extinct lobe-finned fishes called rhipidistians seem to be the most likely tetrapod ancestor Z Similar to modern lungfish -
Chronic Salpingitis in Collared Forest-Falcon (Micrastur Semitorquatus - Vieillot, 1817)
ISSN 2447-0716 Alm. Med. Vet. Zoo. 12 CHRONIC SALPINGITIS IN COLLARED FOREST-FALCON (MICRASTUR SEMITORQUATUS - VIEILLOT, 1817) SALPINGITE CRÔNICA EM GAVIÃO-RELÓGIO (MICRASTUR SEMITORQUATUS - VIEILLOT, 1817) Guilherme Augusto Marietto-Gonçalves* Ewerton Luiz de Lima†, Alexandre Alberto Tonin‡ RESUMO O presente artigo notifica a ocorrência de salpingite crônica em um exemplar de Micrastur semitorquatus cativo, com sete anos de idade, ocorrido no período de seis meses após a submissão de um procedimento emergencial de ovocentese. Devido a apresentação constante de apatia e dificuldade respiratória e de um aumento de volume abdominal a ave seria analisada para a realização de uma laparotomia exploratória. No início de um procedimento anestésico, durante a indução anestésica a ave veio a óbito e no exame necroscópico encontrou-se o oviduto com aumento de tamanho e com deformação anatômica e ao analisar órgão viu-se que estava repleto de conteúdo caseoso e com duas massas ovais de aspecto pútrido. O exame histopatológico revelou um quadro de metrite no terço proximal do oviduto. Apesar de não ter sido realizado uma avaliação microbiológico o quadro observado é compatível com salpingite por colibacilose ascendente. A realização de procedimentos de ovocentese deve ser restrita devido ao risco de lesões iatrogênicas que expõem o trato reprodutivo de aves fêmeas a infecções ascendentes que ofereçam risco de vida para os animais. Palavras chave: distúrbios reprodutivos, rapinantes, Micrastur, patologia aviária ABSTRACT This scientific report notifies the occurrence of chronic salpingitis in a captive Micrastur semitorquatus, ten years old. Salpingitis occured six months after an emergency procedure (ovocentesis). Due to the persistent apathy, difficulty breathing and an increase in abdominal volume, the bird was clinically evaluated in order to perform an exploratory laparotomy. -
Life History Account for American Kestrel
California Wildlife Habitat Relationships System California Department of Fish and Wildlife California Interagency Wildlife Task Group AMERICAN KESTREL Falco sparverius Family: FALCONIDAE Order: FALCONIFORMES Class: AVES B127 Written by: C. Polite, G. Ahlborn Reviewed by: S. Bailey Edited by: S. Bailey DISTRIBUTION, ABUNDANCE, AND SEASONALITY Common resident throughout California, wintering in all habitats except high elevations. Also a winter migrant. Fairly common on Channel Islands. Occurs in most open habitats, in a variety of shrub and early successional forest habitats, in forest openings, and various ecotones. SPECIFIC HABITAT REQUIREMENTS Feeding: Takes small mammals, birds, insects, earthworms, reptiles, and amphibians. Perches and pounces, pounces from a hover, or catches flying insects. Rarely pursues prey on wing. Caches prey near nest in cracks in trees or rocks (Collopy 1973). Perch may be tree, snag, rock, utility pole or wire, fence post (Grinnell and Miller 1944). Forages in open habitats. Cover: Seeks cover in a variety of cavities in trees, snags, rocky areas, banks, and buildings. Reproduction: Nests in cavities in trees, snags, rock crevices, cliffs, banks, and buildings. Bent (1938) reported nests in cavities in sycamores, willows, and cottonwoods. Does not construct a stick nest. Often uses cavities excavated by northern flickers and Lewis' woodpeckers. In Oregon, Thomas (1979) estimated that the minimum dbh tree required by these 2 woodpeckers was 31 cm (12 in) and 38 cm (15 in), respectively. Water: Drinks water in captivity (Roest 1957). Has a high tolerance to heat and aridity. Pattern: Forages in open and partially open areas of most habitats. Needs cavities near foraging areas. -
Characterization of Chromosome Structures of Falconinae
Characterization of chromosome structures of Falconinae (Falconidae, Falconiformes, Aves) by chromosome painting Title and delineation of chromosome rearrangements during their differentiation Nishida, Chizuko; Ishijima, Junko; Kosaka, Ayumi; Tanabe, Hideyuki; Habermann, Felix A; Griffin, Darren K; Author(s) Matsuda, Yoichi Chromosome Research, 16(1), 171-181 Citation https://doi.org/10.1007/s10577-007-1210-6 Issue Date 2008 Doc URL http://hdl.handle.net/2115/44583 Rights The original publication is available at www.springerlink.com Type article (author version) File Information nishida.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Characterization of chromosome structures of Falconinae (Falconidae, Falconiformes, Aves) by chromosome painting and delineation of chromosome rearrangements during their differentiation Chizuko Nishida1, Junko Ishijima1, Ayumi Kosaka1, Hideyuki Tanabe2, Felix A. Habermann3, Darren K. Griffin4 & Yoichi Matsuda1 * 1 Laboratory of Animal Cytogenetics, Creative Research Initiative “Sousei”, Hokkaido University, North 10 West 8, Kita-ku, Sapporo 060-0810, Japan, Tel: +81-11-706-2619; Fax: +81-11-736-6304; E-mail:[email protected]; 2Department of Evolutionary Studies of Biosystems, School of Advanced Sciences, The Graduate University for Advanced Studies, Shonan Village, Hayama, Kanagawa 240-0193, Japan; 3Institute of Veterinary Anatomy, Histology and Embryology, Veterinarstrasse 13, D-80539, Munchen, Germany 4Department of Biosciences, University of Kent,