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Lifespan, longevity, and ageing

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Maximum longevity: 29 years (wild) Observations: Though sexual maturity may be reached at earlier ages, breeding normally does not occur before age 2. The record longevity in the wild is 13 years (http://www.fs.fed.us/database/feis/).
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Behavior ( англиски )

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Great horned owls primarily communicate by hooting. This establishes territorial dominance and is also used to search for mates. Their distinctive territorial call, "hoo-hoo hoooo hoo-hoo," can be heard from miles away. They screech loudly when attacking prey. Sometimes recordings of hooting sounds are used to determine population densities. Great horned owls use their vision to locate prey and navigate in the darkness, even through dense forests. They have binocular vision, which allows excellent frontal vision but weaker peripheral vision. They can lose their vision from trauma, pathogenic infection, and possibly from inherited genetic disorders.

Communication Channels: visual ; acoustic

Perception Channels: visual ; tactile ; acoustic ; chemical

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Conservation Status ( англиски )

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Great horned owls are one of the most widespread and successful bird species in the United States. They are not threatened or endangered.

US Migratory Bird Act: no special status

US Federal List: no special status

CITES: no special status

State of Michigan List: no special status

IUCN Red List of Threatened Species: least concern

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Benefits ( англиски )

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Great horned owls may prey upon poultry raised as livestock.

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Benefits ( англиски )

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Great horned owls feed on species at many different trophic levels, including many rodent and insect species that are considered pests by humans. They can adapt to ecosystems inhabited by humans and can act as a control to an overabundance of these pests.

Positive Impacts: controls pest population

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Associations ( англиски )

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Reproduction of great horned owls is heavily dependent upon prey availability. For example, populations increase when numbers of its primary prey the snowshoe hare, Lepus americanus, were highest. When snowshoe hare abundance lowered, so did the number of great horned owls.

Great horned owls are at risk for parasitism, though it is not always lethal. They can be afflicted with avian malaria if bitten by an infected blackfly. They change nest locations depending on blackfly activity; in the summer when blackflies are active, they roost on or near the ground. In the winter, when fly activity is lower, they will return to the canopy areas.

Commensal/Parasitic Species:

  • Avian malaria Plasmodium relictum
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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Catherine Kent, Special Projects
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Trophic Strategy ( англиски )

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Great horned owls are carnivores that primarily eat terrestrial vertebrates. They have a variable diet that depends on the availability of prey. In late successional areas, they feed on lagomorphs and voles. In the southwestern U.S. where great horned owls are smaller, they often feed on smaller prey like juvenile rabbits and small rodents or insects. In fields and deserts, their primary diet is likely to consist of rodents and insects. In a habitat surrounded by or adjacent to water, they are capable of hunting fish, amphibians, crustaceans, and reptiles. When hunting, they perch and search for prey, then swoop down and catch it while airborne if necessary.

Animal Foods: birds; mammals; amphibians; reptiles; fish; insects; aquatic crustaceans

Primary Diet: carnivore (Eats terrestrial vertebrates)

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Distribution ( англиски )

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Great horned owls are native to a large geographic range that covers most of North America and extends south into Central and South America. Their latitudinal range is from 68 degrees north latitude (around the northern tip of Alaska) to 54 degrees south latitude (near the southern tip of Brazil).

Biogeographic Regions: nearctic (Native ); neotropical (Native )

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Habitat ( англиски )

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Great horned owls are well suited for many habitats and environments. They live at a variety of elevations, from sea level up to 3352.8 meters. Great horned owls are most commonly found in interspersed areas of woodland and open fields. Their habitats include grasslands, deserts, swamps, marshes, mangroves, and both rural and urban human settlements.

Range elevation: 0 to 3352.8 m.

Habitat Regions: temperate ; tropical ; terrestrial

Terrestrial Biomes: tundra ; taiga ; desert or dune ; savanna or grassland ; chaparral ; forest ; rainforest ; scrub forest ; mountains

Aquatic Biomes: coastal

Wetlands: marsh ; swamp ; bog

Other Habitat Features: urban ; suburban ; agricultural ; riparian ; estuarine

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Life Expectancy ( англиски )

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The average life expectancy of great horned owls is 13 years. The record for the longest life in the wild is 28 years old. In captivity, the average lifespan is 20 years and the longest recorded lifespan is 35 years. Human activities such as habitat degradation are also expected to affect their lifespan.

Average lifespan
Status: wild:
28 years.

Average lifespan
Status: captivity:
35 years.

Average lifespan
Status: wild:
13 years.

Average lifespan
Status: captivity:
20 years.

Average lifespan
Status: wild:
333 months.

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Morphology ( англиски )

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Like similar owl species, great horned owls have a rounded facial structure and forward-facing eyes which allow for binocular vision. They have distinctive horn-like feather tufts on the tops of their heads. The tufts are usually darker than the rest of the head, improving camouflage. They have a distinctive white spot on their throat. Their underbellies are white with brown and black 'bars' distributed throughout. They are white or tan colored around a black bill. Their back is darker in color, featuring a mottled blacks and browns. Their eyes are different shades of yellow in color.

The size and of great horned owls varies by their geographic location and their sex. They exhibit reverse sexual dimorphism, where females are slightly larger than males. Females average about 1.7 kg, while males average 1.3 kg. Evidence suggests this dimorphism is not influenced by environmental factors. This conclusion comes from the observation that great horned owls generally do not migrate sufficient distances to cross-breed with subspecies which may differ in size. In northern latitudes, they tend to have larger core bodies and a longer wingspan. Their overall length is 45.7 to 63.5 cm and their wingspan is 127 to 152.4 cm. This is consistent with Bergmann's rule, which states that in broadly-distributed genuses, larger individuals of species are found in northern latitudes, while smaller individuals are found in southern latitudes. Variations in color also exist depending on geographic location. For example, Bubo virginianus saturatus, a woodland-inhabiting subspecies of great horned owl, may have darker, browner coloration. Bubo virginianus elachistus, which lives in desert habitats in Baja California, may have a lighter, grayer coloration.

Average mass: 1.3 (males) 1.7 (females) kg.

Range length: 45.7 to 63.5 cm.

Range wingspan: 127 to 152.4 cm.

Other Physical Features: endothermic ; bilateral symmetry ; polymorphic

Sexual Dimorphism: female larger

Average mass: 1450 g.

Average basal metabolic rate: 5.2442 W.

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Associations ( англиски )

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Great horned owls are at the top of many food chains and are not preyed upon by other species. However, territorial disputes between members of the same species can be fatal. Sometimes crows (Corvus brachyrhynchos) or raccoons (Procyon lotor) eat their eggs, however.

Known Predators:

  • crows (Corvus brachyrhynchos)
  • raccoons (Procyon lotor)
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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Reproduction ( англиски )

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Great horned owls are monogamous, forming a mating pair that raise the young. Breeding pairs are territorial, excluding other breeding pairs from their territory to ensure access to prey. However, they may only display territorial behavior in areas close to their nest and do not completely protect their territory. Mates find one another through 'hooting' rituals, which increase in intensity as the mating season approaches. Males hoot throughout the year, but females only hoot during mating season.

Mating System: monogamous

Great horned owls inhabit nests abandoned by squirrels or other birds, including other great horned owls. Their brood sizes depend on food availability and geographic location. Smaller broods are more common in years with lower prey abundance. On the eastern seaboard, broods than 2 are considered rare. In central and western North America, however, a brood size of 3 to 4 is not uncommon. They have 1 to 6 eggs per season which hatch in 30 to 37 days. Great horned owl chicks fledge in 6 to 9 days and achieve independence at 5 to 10 weeks. They achieve sexual maturity in 1 to 3 years. Like other birds with a large geographic distribution, great horned owls tend to nest later in the year relative to the increase in latitude of their location.

The mating ritual of great horned owls is described 'violent nodding and bowing', followed by a quieter 'billing and cooing' stage that signifies the completion of copulation.

Breeding interval: Great horned owls breed on a seasonal basis.

Breeding season: Breeding occurs between the months of November and April.

Range eggs per season: 1 to 6.

Range time to hatching: 30 to 37 days.

Range fledging age: 6 to 9 weeks.

Range time to independence: 5 to 10 weeks.

Range age at sexual or reproductive maturity (female): 1 to 3 years.

Range age at sexual or reproductive maturity (male): 1 to 3 years.

Key Reproductive Features: iteroparous ; seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate); sexual ; fertilization ; oviparous

Average eggs per season: 3.

Males and females alternate roosting and hunting during the time they are nesting. Males do the majority of the hunting while females spend their time protecting the brood. When prey is scarce, females are more likely to leave the nest unattended to search for additional food, especially if the clutch size is larger than average. The location of their nest varies. In late successional areas, they are more likely to roost in elevated areas (up to 100 feet). In prairies and early successional areas, they set up nests in bushes, cliff nooks, and even on the ground.

Parental Investment: altricial ; male parental care ; female parental care ; pre-hatching/birth (Provisioning: Male, Female, Protecting: Male, Female); pre-weaning/fledging (Provisioning: Male, Female, Protecting: Male, Female); pre-independence (Provisioning: Male, Female, Protecting: Male, Female)

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Dietrich, D. 2012. "Bubo virginianus" (On-line), Animal Diversity Web. Accessed April 27, 2013 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bubo_virginianus.html
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Drew Dietrich, Radford University
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Karen Francl, Radford University
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Kiersten Newtoff, Radford University
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Melissa Whistleman, Radford University
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Catherine Kent, Special Projects
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Amenazas ( шпански; кастиљски )

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Factores de riesgo

Aunque presenta un amplio rango de distribución en toda América, está especie es considerada de común a medianamente común en Norteamérica, pero con densidades bajas, e incluso raro en Centroamérica (Stotz, et al., 1996; Hume, 1997). En las culturas antiguas de Norteamérica, aunque se tenían ideas supersticiosas de la muerte asociadas al búho cornudo, esta especie siempre fue respetada. Sin embargo, a la llegada de los europeos, se inició una larga historia de persecución con este búho. Así que asociada a la pérdida del hábitat (zonas arboladas) en ciertas regiones, y disminución en la disponibilidad de sus presas, un importante factor de riesgo ha sido la persecución de este búho para capturarlo y/o usarlo como tiro de caza. Existe información en Norteamérica que de varios búhos juveniles anillados y posteriormente recuperados, 56 fueron matados con arma de fuego, 41 fueron capturados, 15 colisionaron con automóviles, 14 fueron muertos en caminos y 13 electrocutados en cables eléctricos de luz. Otros factores de riesgo son las colisiones en construcciones humanas y cacería ilegal. El uso de plaguicidas en Norteamérica para control de roedores afecta indirectamente a esta especie. Por lo tanto, su futuro necesita ser considerado de cuidado (Voous, 1989). A pesar de esto, su rango de distribución en el Noroeste de Estados Unidos ha aumentado, debido al incremento de áreas abiertas, ya que presenta alta capacidad de adaptabilidad a cambios en su hábitat. Así mismo en Sudamérica este búho se ha visto beneficiado por la introducción del conejo europeo, siendo el principal alimento para esta especie en Chile (Donázar, et al., 1997).

Situación actual del hábitat con respecto a las necesidades de la especie

Las actividades humanas en todos los tipos de hábitats han influido en diferente grado y escala. Sin embargo, las áreas boscosas son las que han sido más ampliamente afectadas. Pero a pesar que el búho cornudo puede adaptarse a áreas modificadas por el hombre ya que se puede encontrar en paisajes fragmentados, requiere áreas boscosas para su reproducción.
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CONABIO
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Enríquez-Rocha, P.
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Biología ( шпански; кастиљски )

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Historia de la vida

El búho cornudo es residente y puede permanecer en su territorio por varios años. Esta especie es principalmente nocturna, pero puede ser activa al anochecer y/o amanecer. Este búho es considerado de común en Norteamérica a poco común o raro en otras áreas dentro su rango de distribución. Se reproduce desde diciembre en algunas regiones hasta abril o mayo donde se han reportado juveniles. Usualmente utiliza nidos grandes y abandonados de águilas en palmas o en árboles grandes, también se han reportado nidos en el piso o en cuevas (Hilty y Brown, 1986) o incluso en nidos activos de otras aves como garzas o loros (De la Peña, 1986). En ocasiones coloca palitos o plumas sobre el nido. Pone dos huevos aunque con abundante alimento puede llegar a poner hasta seis huevos, estos son blancos y miden de 57 x 46 mm. Ambos miembros de las parejas son muy agresivos a los intrusos durante la temporada de reproducción, principalmente cuando tienen juveniles (König, et al., 1999). Esta especie se ha registrado posando durante el día en la parte media o alta de árboles densos o palmas (Stiles y Skutch, 1989), y habita en áreas abiertas asociadas a áreas boscosas y cercanas a cuerpos de agua. En un estudio en New Jersey el búho cornudo no se asoció con ningún hábitat en particular, siendo una especie generalista en el uso del hábitat (Laiding y Dobkin, 1995). La alimentación de esta especie es muy variada, ya que es una especie generalista y oportunista. Sin embargo, los mamíferos son la base de su dieta, algunas de las presas registradas como alimento son conejos, ratones, coatis, zorrillos, tlacuaches, y diferentes especies de aves, reptiles e insectos. En general es una especie sedentaria, pero puede realizar movimientos en algunos años si el alimento escasea o no está disponible. En Canadá se recuperaron anillos de individuos marcados con distancias más allá de 250 Km del punto de anillamiento. El búho cornudo habita en ocasiones cercano a otras rapaces como el aguililla real (Buteo regalis), el águila real (Aquila chrysaetos) y el halcón peregrino (Falco peregrinus). Sin embargo, otras especies de búhos medianos como el búho cara café (Asio otus) y el búho cuerno corto (A. flammeus) son ausentes o excluidos de los territorios de este búho (Johnsgard, 1988). Aparentemente los tumores en aves son muy raros, pero se han reportado tumores en el búho cornudo (Swayne y Weisbrode, 1990).
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CONABIO
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Biología de poblaciones ( шпански; кастиљски )

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Tamaño poblacional

La densidad poblacional varía según la región, pero en algunas áreas esta densidad está relacionadas con la abundancia de sus presas. El búho cornudo es considerado poco común en poblaciones del sur, y es raro en Centroamérica. Se han estimado densidades para el búho cornudo en Norteamérica de 0.1- 0.2 parejas/Km2, de 1 a 3 parejas por 2.6 km2, una pareja por 5.2 km2, o una pareja por 0.65 a 0.86 km2 (Eaton 1988, Johnsgard 1988). En Kansas se registró una pareja por 2.6 km2. En Michigan una pareja por 13.7 km2. En Alberta, Canadá se registró una densidad de una pareja por 10.1 km2. Sin embargo, otros datos reportan que el promedio de territorio de tres parejas es de 105 ha. En New York las poblaciones de esta especie en zonas urbanas y suburbanas parecen ser estables (Minor, et al., 1993).

Reclutamiento

La supervivencia del búho cornudo generalmente es baja durante los dos primeros años de vida, aunque está aumenta cuando la disponibilidad de alimento se incrementa, por ejemplo, relacionado a los ciclos poblacionales de roedores y liebres (Voous, 1989). El éxito reproductivo y mayor número de parejas reproductoras también están asociados a los picos poblacionales de roedores. En Ohio la productividad media anual fue de 1 a 7 juveniles por nido. En New York la productividad media de 34 individuos de esta especie en una área urbana/suburbana fue de 1.63±0.16 volantones por nido, con un rango de 0.5 a 0.3 juveniles/nido, y con un promedio de densidad de 0.02± 0.003 parejas andantes/km2 (Minor, et al., 1993). La mortalidad anual de esta especie después de su segundo año de vida fue de 28-32% (Johnsgard, 1988). Los factores de mortalidad en volantones incluyen muertes por parasitismo, por depredación, por enfermedad o falta de alimento, y muerte en caminos. La máxima longevidad registrada para esta especie ha sido más de 28 años.

Antecedentes del estado de la especie o de las poblaciones principales

El búho cornudo presenta una amplia distribución en América. Sin embargo, es considerado desde común en Norteamérica a medianamente común o raro en algunas regiones de México y Centroamérica (Howell y Webb, 1995; Stotz, et al., 1996).
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Biología del taxón ( шпански; кастиљски )

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Relevancia de la especie

El búho cornudo es una especie depredadora y es considerada un elemento importante en la estructura y función de los ecosistemas donde habita. Esta especie puede ser considerada reguladora de especies de mamíferos pequeños o medianos, como lo son aquellas especies de roedores introducidas a América de Europa (Donázar, et al., 1997).
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Comportamiento ( шпански; кастиљски )

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Residente y nocturno.

Ámbito hogareño

Especie territorial. El área de acción estimada en promedio para esta especie es de 329 ha pero decrece en primavera cuando la disponibilidad de alimento incrementa o aumenta en verano cuando el alimento disminuye (Johnsgard, 1988). Otras estimaciones han reportado área de acción promedio de 16 km2, pero también reportes de áreas de acción tan pequeñas como 2.6 km2. En Columbia River en Washington los nidos del búho cornudo fueron separados por 0.8 a 10.3 km, con promedio de 3.9 Km (Voous, 1989). El promedio de territorio de tres parejas fue de 105 ha. En Alberta, Canadá se registro una densidad de una pareja por 10.1 km2. En Kansas se registró una pareja por 2.6 km2 y en Michigan una pareja por 13.7 km2.
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Conservación ( шпански; кастиљски )

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El búho cornudo fue fuertemente perseguido en la primera mitad del siglo XX, pero protegido posteriormente en Estados Unidos en 1970. En México se necesitan más estudios biológicos y ecológicos con esta especie para tener mejores bases sobre su status, manejo y conservación.
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Descripción ( шпански; кастиљски )

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De las once especies del género Bubo que se distribuyen en el mundo, el búho cornudo es el único miembro de este género en América (Voous, 1989). En ocasiones esta especie ha sido considerada dentro de Bubo bubo. Sin embargo, estudios con vocalizaciones, con DNA, y morfológicos han mostrado ciertas diferencias entre ambas especies. El búho cornudo es de gran tamaño, y es la especie de búho más grande en los Neotrópicos. Aunque presenta una gran variación en su tamaño dentro de su rango de distribución, este tamaño no es consistente con la latitud (McGillivray, 1989). Ambos sexos son semejantes, pero los machos son más pequeños que las hembras, estos miden 51 cm de longitud aproximadamente y las hembras 60 cm, pesan de 680 g a 2500 g. Aparentemente los organismos en áreas tropicales y desiertos son más pequeños (45 cm). El búho cornudo presenta un disco facial de café a anaranjado con un borde blanquecino alrededor de los ojos y una corona obscura. Presenta plumas grandes a manera de cuernos u orejas, los ojos son amarillos y el pico es grisáceo. El plumaje del cuerpo es un distintivo color gris o café-grisáceo con blanco-amarillento y barrado de negro o café en las partes bajas del cuerpo, presenta un plumaje blanco alrededor de la garganta. Las alas son largas, las plumas del vuelo y de la cola son barradas de coloración obscura. Los tarsos y los dedos están completamente emplumados y en ocasiones con barras obscuras. El plumaje es más oscuro en climas cálido- húmedos, y más claro en climas fríos (Voous, 1989). Habita en una gran variedad de hábitats por lo que existe un amplio rango en tamaño y coloración. Los juveniles son similares a los adultos pero de coloración más café-anaranjado y con barras menos frecuentes, la banda blanca de la garganta está menos extendida que en los adultos, y las plumas a manera de cuernos son más cortas (Álvarez del Toro, 1971; Marks, et al., 1999). La vocalización del macho es más prolongada y elaborada que el de la hembra. Cuando estos búhos están alterados la vocalización sigue a unos cortos ladridos, aunque no es tan fuerte como en el búho barrado (Johnsgard 1988). Durante el cortejo ambos miembros de la pareja vocalizan a dúo. La vocalización es una serie de fuertes notas "hu-huhoooo, hooh hooh" y la hembra vocaliza más agudo con notas al inicio "hu-huhuhoo hooh hooh". Se han descrito varias subespecies, muchas de ellas representan variaciones individuales, formas o tipos intermedios en coloración (Marks, et al., 1999). Las subespecies aparentemente tienden a variar en tamaño siendo las más pequeñas de Noroeste a Suroeste y son de coloración más obscura en regiones húmedas. König, et al. (1999) reconocen diez subespecies y Marks, et al. (1999) reconocen doce subespecies, estas son: B. v. lagophonus (Oberholser, 1904) desde el Sur de Alaska hasta el noreste de Oregon y noroeste de Montana, en el invierno se puede encontrar hasta el sur en Texas; B. v. saturatus Ridgway, 1877 en la costa desde el sureste de Alaska hasta el norte de California; B. v. pacificus Cassin, 1854 desde la costa de California hacia el Sur hasta el Noroeste de Baja California en México; B. v. elachistus Brewster, 1902 Baja California Sur; B. v. subarticus Hoy, 1853 desde el Noroeste de Columbia Británica hasta la Bahía de Hudson, hasta el sur en Wayoming y Dakota del Norte, Sur de Arizona, Nuevo México y Suroeste de Texas; B. v. pallescens Stone, 1897 desde el centro de California y desiertos del sureste de California hasta el oeste de Kansas, y sur de México hasta el sur de Guerrero y oeste de Veracruz; B. v. heterocnemis (Oberholser, 1904) desde el Noreste de Canadá hasta la región de los Grandes Lagos; B. v. virginianus (Gmelin, 1788) desde el este de Minnesota hasta Nova Scotia y la Isla de Prince Edward hasta el este de Kansas, este de Texas hasta Florida; B. v. mayensis Nelson, 1901 Península de Yucatán; B. v. mesembrinus (Oberholser, 1904) del Istmo de Tehuantepec hasta el oeste de Panamá; B. v. nigrescens Berlepsch, 1884 en los Andes, desde Colombia hasta el noroeste de Perú; B. v. nacurutu (Vieillot, 1817) desde las tierras bajas del este de Colombia hasta las Guianas, también Bolivia, noroeste de Brasil hasta Argentina (Marks, et al., 1999).
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Distribución ( шпански; кастиљски )

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Histórica-actual

MEXICO

Distribución histórica: El búho cornudo presenta una amplia distribución, desde la región Neártica en Alaska hasta Argentina en Sudamérica. Se puede distribuir en casi todos los climas, con excepción de la tundra y áreas tropicales lluviosas donde ocurre esporádicamente. La distribución de esta especie es muy local y rara en zonas bajas húmedas de Centro y Sudamérica, pero se encuentra más ampliamente distribuida en zonas frías de tierras altas y zonas templadas (Meyer de Schauensee, 1970; Ridgely y Gwynne, 1989). Los reportes de colecta más antiguos para esta especie en México han sido en Baja California en 1859, Zacatecas en 1889, Nayarit en Cerro Tepic en 1891, Jalisco en 1891, Coahuila en 1899, Chihuahua en 1905, Sonora en 1905, Baja California en San Pedro en 1909, y Baja California en Miraflores en 1911. Los registros más recientes se encuentran en San Roberto, Nuevo León en 1960; en Monte Largo, Sinaloa a 20 Km oeste de Pericos en 1960; a 13 Km al este de Bahía Kino, Sonora en 1960; en Paso de Cortés, Puebla en 1961; a 66 km al sur de la ciudad de San Luis, San Luis Potosí en 1970; en San Andrés, Zacatecas en 1972; en Presa Noria Ramos Arizpe, Coahuila en 1978 y 1983. En Chiapas se ha colectado en la parte más seca de la costa, en la región central del estado y en la zona norte cerca de Yajalón (Álvarez del Toro, 1971). En Sonora se distribuye prácticamente en todo el estado (Rusell y Monson, 1998). En Oaxaca se ha reportado en la Región de Rancho de Cacoprieto en Tehuantepec, San Miguel Suchixtepec, y Noreste de San Andrés Chicahuaxtla (Binford, 1989).

Distribución actual: La distribución actual para el búho cornudo en México es muy amplia, abarca desde el norte de México incluyendo Baja California Norte y Sur, hasta el sur de México incluyendo la Península de Yucatán (Howell y Webb, 1995). Aunque el búho cornudo aparentemente presenta una amplia distribución en todo el país, muy poca información existe sobre el estado actual de sus poblaciones y sobre su rango de distribución actual en México.
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Estrategia trófica ( шпански; кастиљски )

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El búho cornudo es una especie generalista y oportunista por lo que se alimenta de una gran variedad de presas las cuales incluye pequeños y medianos mamíferos, aves, anfibios, reptiles, peces, insectos y otros invertebrados. En ocasiones puede alimentarse de carroña cuando las condiciones ambientales son severas. El 77.6% de las presas consumidas en Norteamérica consisten en mamíferos, el 6.1% en aves, y el 1.6% de otros vertebrados. Pero a menudo el 90% de la dieta son lagomorfos, ratones y aves acuáticas. Los mamíferos son la dieta más importante, entre las que destacan Thomomys bottae, Neotoma fuscipes, Mus musculus, Microtus californicus, Peromyscus sp., Zapus sp, Mus sp, Sylvilagus sp., Sorex ornatos, Rattus sp. Dentro de las aves, se han registrado alrededor de 50 diferentes especies, como especies de pájaros bobos (Sula sp.), patos (Anas sp), gansos, cisnes, y varias especies de garzas. En Pennsylvania se alimenta de la rata de Noruega (Rattus norvegicus), (Permoyscus leucopus), del carpintero de pechera (Colaptes auratus) y del tlacuache (Didelphia marsupiallis). En el norte de Canadá se alimenta de liebres (Lepus americanus) las cuales representaron el 83-86% hasta el 13% de la dieta dependiendo de la densidad de las liebres, presentando una respuesta numérica a los ciclos poblacionales de las liebres (Marks, et al., 1999). Los hábitos alimentarios reportadas para esta especie en los Neotrópicos han sido poco estudiados. En Baja California las presas más consumidas fueron los roedores y lagomorfos (Lepus californicus, Sylvilagus audoboni, Peronthus spp, Neotoma lepida, Dipodomys merriami, Peromyscus eva). Los artrópodos fueron el segundo grupo más consumido, entre los que destacaron los insectos como Grillidae y Cerambicidae, algunos reptiles como lagartijas (Phrynosoma coronatus, Seloporus sp.) y serpientes. Las presas menos frecuentes fueron las aves, arañas (Lycosa sp., Olios sp.) y escorpiones (Llinas-Gutiérrez, et al., 1991). En Sonora se han registrado las siguientes presas: Mamíferos Rodentia (Perognathus sp, Dipodomys deserti, D. merriami, Neotoma sp, Sigmodon sp, Sylvilagus sp), aves (Falco sparverius, Tyto alba, Athene cunicularia, Phalaenoptilus nutallii), reptiles (Sauromalus obesus, Uta sp.), Arachnida, Insecta: Orthoptera (Tettigonidae, Acrididae), Coleóptera, (Wink, et al., 1987). En Sudamérica se tienen registros de monos y otros marsupiales como alimento de esta especie. En Surinam el búho cornudo consume tlacuaches (didelphidos), monos y garzas. En Chile se incluyen pequeños mamíferos como Orysomys longicaudatus, Reithrodon physodes, Akodon xanthorhinus, A. lanosus, Rattus norvegicus, R. rattus, Phyllotis darwini; Arachnida: Grammostola sp, Insecta: Tenebrionidae, Carabidae, Tettigonidae, Grillidae, Acrididae (Jáksic et al., 1978; Yañez, et al., 1978). Jáksic, et al. (1978) concluyeron que el búho cornudo captura y consume las especies más abundantes. En Argentina también los mamíferos son las principales presas de esta especie (69%) las que sobresalen Reithrodon auritus, R. physodes, Lepus europaeus, L. capensis, Ctenomys haigi, Abrothrix longipilis, A. xanthorhinus, Eligodontia morgani, Oligoryzomys longicaudatus. Los artrópodos representaron el 27% de las presas donde sobresalieron los escarabajos y escorpiones (Coleoptera, Araneae, Scorpionida), la mayor biomasa provino de especies de mamíferos introducidos como L. europaeus y Oryctolagus cuniculus. Las aves (e.g. Tyrannidae, Anas sp, Falco sparverius, Zenaida auriculata), así como los reptiles (Iguanidae) y anfibios aunque fueron consumidos no fueron bien representados (Iriarte, et al., 1990; Donázar, et al., 1997; Trejo y Grigera, 1998). Generalmente este búho forrajea al anochecer y durante la noche, y rara vez durante el día. En regiones desérticas consume lagartijas las cuales captura en la tarde. El búho cornudo caza desde la percha pero también sobre el piso en áreas abiertas y semi-abiertas en bordes de bosques (König, et al., 1999). Esta especie puede matar a otras especies de búhos como el búho cuerno corto (Asio flammeus), el búho listado (Strix varia), el tecolote llanero (Athene cunicularia), y varias especies de pequeños tecolotes (Otus sp.) (Hume, 1997).
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Hábitat ( шпански; кастиљски )

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El búho cornudo vive en un amplio rango de tipos de vegetación, desde bosques deciduos, bosques mixtos de pino-encino, manglares (Avicennia), bosques pantanosos, desiertos, páramos, vegetación secundaria, áreas abiertas asociadas a zonas boscosas, plantaciones de café y pastizales con árboles aislados. Esta especie está asociada a paisajes fragmentados y considerado tolerante a las actividades humanas, se puede observar ocasionalmente en parques, en ciudades y pueblos (Eaton, 1988).

Macroclima

Habita en un amplio rango de hábitats, desde regiones boscosas en bosques boreales del norte, bosques tropicales en zonas bajas, bosques decíduos, bosques pantanosos, manglares, desiertos, páramos, bosques de coníferas, hasta vegetación secundaria, áreas abiertas, tierras de cultivo asociadas a áreas boscosas y en grandes parques en pueblos. Altitud: Nivel del mar - 4000 m y 4500 msnm en los Andes de Ecuador y Perú (Howell y Webb, 1995; Hume, 1997).

Tipo de ambiente

Posiblemente ningún otro búho en Norteamérica vive en una gran variedad de hábitats y tipos diferentes de climas como el búho cornudo. Estos hábitats regularmente están asociados a paisajes fragmentados (Morrell y Yahner, 1994). Sin embargo, en Honduras esta especie está restringida en el interior de zonas boscosas arriba de 900 msnm (Monroe, 1968). En Baja California el tipo de vegetación donde habita el búho cornudo es: Mesquite (Prosopis articulata), manglar (Maytenus phylantoides), Bursera spp, y Cactus (Opuntia spp, Machaerocereus gummosus) (Llinas-Gutiérrez, et al., 1991).

Uso de hábitat

El búho cornudo usa un amplio rango de tipos de vegetación que incluye bosques deciduos, bosques de confieras de pino-encino, manglares, bosques pantanosos, desiertos, páramos, y vegetación secundaria. También está asociado a paisajes fragmentados ya que es considerado tolerante a las actividades humanas.
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Reproducción ( шпански; кастиљски )

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Especie monógama y territorial, aparentemente forma parejas para toda la vida. En Norteamérica este búho se encuentra entre las aves que se reproducen primero. El período reproductivo inicia en diciembre o enero. En Florida se reproduce a partir de diciembre y en otras regiones más frías a partir de febrero. En México se han registrado nidos de diciembre a mayo. La puesta de huevos es regularmente de 1 a 3 huevos, pero usualmente pone dos, aunque existen reportes de hasta 5 o 6 huevos cuando existe gran cantidad de alimento. El intervalo de las puestas entre huevos es de 72 horas. Los huevos blancos son incubados de 28 a 35 días por la hembra. La hembra es alimentada por el macho. Los pollos permanecen en el nido más de 7 semanas y posteriormente empiezan a escalar las ramas de los árboles. Los pollos no volarán hasta la semana décima o doceava y los padres cuidarán de ellos por 5 meses más, por lo que los padres alimentan a los pollos o juveniles hasta el otoño. Los adultos son muy agresivos cuando tienen pollos o juveniles. Si la nidada fracasa, esta puede ser reemplazada. El búho cornudo alcanza la madurez sexual durante el segundo año de vida, pero algunas veces en su primer año. Esta especie puede anidar en cavidades grandes de árboles, o en depresiones naturales en la base de ramas, en riscos, en cuevas, entre rocas o incluso en el piso, se adiciona muy poco material al nido, pero se acumulan plumas (Hume, 1997). También utiliza grandes nidos abandonados o viejos de otras aves como el de la aguililla cola roja (Buteo jamaicensis), del águila pescadora (Pandion haliaetus), del aguila calva (Haliaeetus leucocephalus), de cuervos (Corvus brachyrhynchos) y de garzas (Eaton, 1988). Puede utilizar el mismo nido 2 o 3 veces consecutivas si se encuentra en buenas condiciones. En Ohio se han registrado nidos de esta especie en colonias de reproducción de garzas, usando nidos viejos dentro de la colonia o quizás puede tomar nidos nuevos de otras aves como el de la garza tigre mexicana (Tigrisoma mexicanum), de loros (Myiopsitta monacha) u otras aves como la gallareta americana (Fulica americana), el pato golondrino (Anas sp., Anas acuta) y la garza morena (Ardea herodias) (Houston y Whitfield, 1975; De la Peña, 1986; Enríquez y Rangel-Salazar, 1996). En un estudio se registraron 533 nidos del búho cornudo en nidos de halcones, 527 en árboles muertos, 125 en plataformas hechas por el hombre, y raramente en construcciones. Otros reportes mencionan que de 86 nidos reportados en Indiana y Ohio, 44 fueron en huecos de árboles y árboles muertos, el resto fueron en nidos del aguililla cola roja. En Baja California se localizó un nido sobre un cactus (Pachycereus pringlei) a una altura de 4.3 m (Llinas-Gutiérrez, et al., 1991). El aguililla cola roja y el búho cornudo anidan aproximadamente a una distancia de 200 m separados uno de otro, esta proximidad se puede explicar por la limitada disponibilidad de sitios para reproducirse. El búho cornudo tiene éxito en anidar cerca de sitios habitados por el hombre (Minor, et al., 1993).
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Enríquez-Rocha, P. 2005. Ficha técnica de Bubo virginianus. En: Escalante-Pliego, P. (compilador). "Fichas sobre las especies de Aves incluidas en el Proyecto de Norma Oficial Mexicana PROY-NOM-ECOL-2000. Parte 2". Instituto de Biología, Universidad Nacional Autónoma de México. Bases de datos SNIB-CONABIO. Proyecto No. W042. México, D.F.
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Bubo virginianus

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A large (18-25 inches) owl, the Great Horned Owl is most easily identified by its brown body, flat disk-shaped face with large yellow eyes, and large brown “ear” tufts. This species may be distinguished from the similarly-sized Barred Owl (Strix varia) by that species’ lack of ear tufts and brown eyes. Male and female Great Horned Owls are similar to one another at all seasons. The Great Horned Owl is the most widely distributed owl species in the Americas. This species occurs from Alaska and northern Canada south to Central America, and South American populations occur from Venezuela south to southern Argentina and Chile. All populations of Barred Owl are non-migratory. Great Horned Owls may be found in a number of woodland habitat types across this species’ wide range, from cold evergreen woodland in the far north and south to humid tropical forest near the equator. Within these habitats, Great Horned Owls prefer open areas along woodland edges, frequently venturing outside the forest into nearby fields and meadows to hunt. Great Horned Owls eat small animals, including rodents, rabbits and hares, and small to medium-sized birds. Great Horned Owls use their excellent hearing to locate prey on the ground in order to fly down and capture it with its talons. Also, like most owls, this species hunts primarily at night, making it difficult to observe. Great Horned Owls are most visible roosting high in trees during the day, and may best be located while producing this species’ characteristic hooting calls between dawn and dusk.

Threat Status: Least Concern

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Reid Rumelt
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DC Birds Brief Summaries

Brief Summary ( англиски )

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The Great Horned Owl is the most common and widespread large owl found in the Americas. Its range spans much of the New World from the Arctic tundra to the tip of South America. A variety of subspecies are recognized based on regional differences in size and color. Throughout its range, this owl has adapted to many different habitats and climates from temperate forests, tropical rainforests, and deserts to agricultural fields and urban parks, but it is generally more common in open, fragmented areas than in dense primary forests.

The Great Horned Owl is characterized by prominent ear tufts or "horns" from which it derives its name. It has large yellow eyes surrounded by a tawny facial disk. A conspicuous, narrow, white patch is often visible on the throat. The adult plumage is mottled and varies in color from reddish brown to light or dark grey. The underside usually has fine dark bars on a lighter background. These owls also have large feet that are feathered down to the strong, heavy talons. Immature owls resemble the adults, but their plumage color is generally lighter or more reddish. Their ear tufts are smaller and the white throat patch is not yet distinctive.

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Bubo virginianus ( англиски )

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A large (18-25 inches) owl, the Great Horned Owl is most easily identified by its brown body, flat disk-shaped face with large yellow eyes, and large brown “ear” tufts. This species may be distinguished from the similarly-sized Barred Owl (Strix varia) by that species’ lack of ear tufts and brown eyes. Male and female Great Horned Owls are similar to one another at all seasons. The Great Horned Owl is the most widely distributed owl species in the Americas. This species occurs from Alaska and northern Canada south to Central America, and South American populations occur from Venezuela south to southern Argentina and Chile. All populations of Barred Owl are non-migratory. Great Horned Owls may be found in a number of woodland habitat types across this species’ wide range, from cold evergreen woodland in the far north and south to humid tropical forest near the equator. Within these habitats, Great Horned Owls prefer open areas along woodland edges, frequently venturing outside the forest into nearby fields and meadows to hunt. Great Horned Owls eat small animals, including rodents, rabbits and hares, and small to medium-sized birds. Great Horned Owls use their excellent hearing to locate prey on the ground in order to fly down and capture it with its talons. Also, like most owls, this species hunts primarily at night, making it difficult to observe. Great Horned Owls are most visible roosting high in trees during the day, and may best be located while producing this species’ characteristic hooting calls between dawn and dusk.

Наводи

  • Bubo virginianus. Xeno-canto. Xeno-canto Foundation, n.d. Web. 20 July 2012.
  • Great Horned Owl (Bubo virginianus). The Internet Bird Collection. Lynx Edicions, n.d. Web. 20 July 2012.
  • eBird Range Map - Great Horned Owl. eBird. Cornell Lab of Ornithology, N.d. Web. 20 July 2012.

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Smithsonian Institution
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Rumelt, Reid B. Bubo virginianus. June-July 2012. Brief natural history summary of Bubo virginianus. Smithsonian National Museum of Natural History, Washington, D.C.
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Robert Costello (kearins)
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Nesting ( англиски )

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Great Horned Owls are opportunistic nesters building their crude nests on a variety of substrates including trees, cliffs, stream banks, columnar cacti, and human-made structures. They often take over abandoned nests of other large birds such as hawks, raven, or crows.
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Associated Plant Communities ( англиски )

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More info for the terms: cover, density, grassland, tree, woodland

Great horned owls occupy a wide variety of forested habitats including
open coniferous and deciduous forests, mixed woods, orchards, second
growth forests, marshes, swamps, riverine forests, partially wooded
slopes, brushy hillsides, farm woodlots, and large city parks [13]. In
the western states great horned owls are often found in oak (Quercus
spp.) and pinyon (Pinus spp.)-juniper (Juniperus spp.) woodland [40].
In Idaho great horned owls are common wherever trees are large enough
for shelter [8]. In west-central Utah great horned owls are permanent
residents in pinyon-juniper woodlands [18]. In the Little Missouri
National Grasslands of western North Dakota, great horned owls were
observed in cottonwood (Populus spp.) woodlands but not in ash (Fraxinus
spp.) or juniper types. In this area, cottonwoods were lower in total
tree density but had higher canopy coverage than other types. In
cottonwood woodlands ground cover was 20 percent, dominated by grasses
[20]. In northeastern Wyoming great horned owls occupy riparian areas
dominated by eastern cottonwood (P. deltoides) and willows (Salix spp.)
surrounded by upland big sagebrush (Artemisia tridendata)-grassland
(primarily Agropyron) communities [33]. In Ohio, great horned owls
occur in virgin American beech (Fagus grandifolia)-maple (Acer spp.)
forests [1]. In the southeastern United States great horned owls are
common in baldcypress (Taxodium distichum) swamps and expansive, dense
cabbage palmetto (Sabal palmetto)-pine woodlands [13].

Andersen [4] listed the great horned owl as a secondary grassland
raptor; it sometimes breeds in grasslands but more typically breeds in
woodlands, edge communities, or partly open habitats.


REFERENCES :
NO-ENTRY
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Common Names ( англиски )

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great horned owl
big-eared owl
hoot owl
cat owl
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Cover Requirements ( англиски )

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More info for the term: tree

Nesting: The great horned owl usually uses nests that were built by
other bird species, especially hawks (Buteonidae), herons (Ardeidae),
and crows (Corvus spp.) [14], but also common ravens (C. corax),
ferruginous hawks (Buteo regalis), and red-tailed hawks (B.
jamaicensis). Great horned owls also use nest cavities excavated by
pileated woodpeckers (Drycopus pileatus) [18]. In northeastern Wyoming
great horned owls use nests of golden eagle (Aquila chrysaetos),
ferruginous hawk, red-tailed hawk, and Swainson's hawk (B. swainsonii)
[33]. Great horned owl nests are up to 70 feet (21 m) above ground in
cavities, tree limb crotches, stumps, caves, and rocky crevices, and on
ledges [14,33]. In the Great Basin great horned owls nested in juniper
trees, on cliffs, and in abandoned quarries with steep fronts [18]. The
great horned owl commonly uses the same territory but a different nest
each season. In Wyoming one pair continuously occupied the same
territory for 7 successive years and another pair held a territory for 8
years. Great horned owls occasionally reuse the same nest in successive
breeding seasons [7].

Roosting: Great horned owls usually roost in places that allow maximum
concealment during daylight hours. They often choose trees with dense
foliage that are separated from other trees in the area. Conifers are
favored when present; in deciduous forests great horned owls prefer
trees that hold clusters of dead leaves over the winter (i.e., oaks and
American beech) [24].

In urban settings, great horned owls nest in deserted buildings,
powerline towers, haylofts of abandoned barns, and artificial nests
[10].

Hunting: Great horned owls often hunt from perches adjacent to open
areas. They usually fly below the treetops but occasionally fly
slightly higher [25].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Distribution ( англиски )

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The great horned owl breeds from western and central Alaska and central
Yukon east to Labrador and Newfoundland and south throughout North and
South America to Tierra del Fuego. Winter range is essentially the same
except for some migration to the southeast by northern populations,
usually in severe winters [14].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Food Habits ( англиски )

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More info for the terms: forest, litter

The great horned owl uses a wide variety of prey and takes animals up to
the size of young wild turkey (Meleagris gallopavo) and common porcupine
(Erethizontidae dorsatum). Small- to medium-sized mammals and birds are
preferred, including hares and rabbits (Leporidae), mice (Muridae),
Virginia opossum (Didelphis virginiana), common muskrat (Ondatra
zibethicus), squirrels (Sciuridae), pocket gophers (Geomyidae), and
voles (Microtus spp.) [12]. Great horned owls also take reptiles
(including snakes), amphibians, large insects, and fish [12,14]. In the
Sierra Nevada 61 percent of great horned owl diet consisted of
cottontails; woodrats (Neotoma spp.) were the second most consumed food
item. Pocket gophers and snakes were minor dietary components. In
Oklahoma 25 percent of great horned owl diet was cottontails, 18 percent
pocket mice (Perognathus spp.), 12 percent kangaroo rats (Dipodomys
spp.), and 10 percent grasshopper mice (Onychomys spp.) [40]. Other
prey items include skunks (Mephitis and Spilogale spp.), ducks and geese
(Anatidae), ring-necked pheasant (Phasianus colchicus), grouse
(Phasianidae), domestic chickens, woodpeckers (Picidae), orioles
(Icterus spp.), and jays (Corvidae) [12]. Large prey can include small
dogs, domestic cats, and young foxes (Vulpes and Urocyon spp.) [10,25].
Predation on songbirds is minimal [12]. In northeastern Wyoming
riparian areas and adjacent big sagebrush-grasslands, the prey base for
great horned owls consists largely of white-tailed jackrabbit (Lepus
townsendii), cottontails, and black-tailed prairie dog (Cynomys
ludovicianus). Other mammals and reptiles are common prey items [33].

Hunting Style: Great horned owls usually hunt from a perch at the edge
of a clearing, making short flights out to capture prey. They also
forage on the wing. On occasion, great horned owls have been observed
walking on the forest floor turning over litter and other materials to
find insects, mice, and shrews (Soricidae). Great horned owls wade into
shallow water for crayfish, fish, frogs, and turtles [24,25].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Habitat-related Fire Effects ( англиски )

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More info for the terms: competition, cover, density

The effects of fire on prey species are probably the most important
habitat related fire effects on great horned owls. Prey availability is
often enhanced by removal of surface cover. Decreases in prey
populations after fire probably result in lowered nesting success or
even a change in residency for great horned owls. In California, great
horned owl density was high following a fire in chaparral, but
reproductive success decreased later, possibly because loss of habitat
concentrated raptors into a smaller area and led to increased
competition for prey [42].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Habitat: Cover Types ( англиски )

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More info on this topic.

This species is known to occur in association with the following cover types (as classified by the Society of American Foresters):

The great horned owl occurs in all SAF types.
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Habitat: Ecosystem ( англиски )

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More info on this topic.

This species is known to occur in the following ecosystem types (as named by the U.S. Forest Service in their Forest and Range Ecosystem [FRES] Type classification):

More info for the term: shrub

FRES10 White-red-jack pine
FRES11 Spruce-fir
FRES12 Longleaf-slash pine
FRES13 Loblolly-shortleaf pine
FRES14 Oak-pine
FRES15 Oak-hickory
FRES16 Oak-gum-cypress
FRES17 Elm-ash-cottonwood
FRES18 Maple-beech-birch
FRES19 Aspen-birch
FRES20 Douglas-fir
FRES21 Ponderosa pine
FRES22 Western white pine
FRES23 Fir-spruce
FRES24 Hemlock-Sitka spruce
FRES25 Larch
FRES26 Lodgepole pine
FRES27 Redwood
FRES28 Western hardwoods
FRES29 Sagebrush
FRES30 Desert shrub
FRES31 Shinnery
FRES32 Texas savanna
FRES33 Southwestern shrubsteppe
FRES34 Chaparral-mountain shrub
FRES35 Pinyon-juniper
FRES36 Mountain grasslands
FRES37 Mountain meadows
FRES38 Plains grasslands
FRES39 Prairie
FRES40 Desert grasslands
FRES41 Wet grasslands
FRES42 Annual grasslands
FRES44 Alpine
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Habitat: Plant Associations ( англиски )

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More info on this topic.

This species is known to occur in association with the following plant community types (as classified by Küchler 1964):

The great horned owl occurs in all Kuchler types.
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Habitat: Rangeland Cover Types ( англиски )

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More info on this topic.

This species is known to occur in association with the following Rangeland Cover Types (as classified by the Society for Range Management, SRM):

More info for the term: cover

The great horned owl occurs in most SRM cover types.
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Management Considerations ( англиски )

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More info for the terms: cover, density, forest, presence, tree, woodland

Population Stability: The great horned owl is a widespread and common
raptor. All the midwestern states report great horned owls as common to
abundant, and they are common to abundant in the Great Plains. Most
great horned owl populations are currently stable or increasing. Only
on the High Plains Border and the Unglaciated Missouri Plateau
physiographic provinces did Breeding Bird Survey data suggest declining
populations [32]. Nesting densities and territory sizes fluctuate
annually, probably due to changes in food supply. In Wyoming a
particularly small nesting population was observed in the same year that
cottontail populations were unusually low. Temporary declines in prey
base are unlikely to cause any long-term great horned owl population
perturbations since great horned owl pairs unsuccessful breeders one
year are often successful in other years [34]. Only the most general
raptor management considerations need to be made for great horned owls,
such as retention of cavity trees, protection of riparian woods within
grasslands, and protection from human harassment [30,33].

Forest Composition: In the northeastern United States, woods consisting
of hardwoods and pines are good habitat for great horned owl and other
raptors (barred owl [Strix varia], northern goshawk [Accipiter
gentilis], broad-winged hawk [Buteo platypterus], and red-tailed hawk).
Forest unit management guidelines should be set in relationship to
selected home range size; since the great horned owl has a very large
home range, managers should consider forest composition objectives in
groups of units rather than individual units. All cavity trees and at
least 10 percent of remaining forest cover should be mature and/or
decadent trees. Silviculture treatments favoring raptors in the White
Mountain National Forest, New Hampshire, included one 0.25- to 0.5-acre
(0.1-0.2 ha) plot left uncut for every 10 acres (4 ha) cut in
regeneration plots. Uncut areas contained at least one living tree 18
inches (45.7 cm) or more in diameter with at least two major defects.
Wherever possible, uncut areas included existing raptor nests (any
species, since great horned owls use old nests of other raptors) [28].
Similarly, in Utah wildlife management considerations included leaving
large old trees for cavity nesters. Woyda and Kessler [43] were of the
opinion that harvest patterns that result in even-aged regeneration
would only be appropriate for great horned owl and other species that do
not require a variety of tree age classes.

Young [44] lists the great horned owl as capable of persisting in
agricultural areas; nesting densities are strongly influenced by
intensity of land use, agricultural practices, and human activity.
Winter use of agricultural areas by great horned owls is common [44].

Artificial Nests: Great horned owls use artificial nests when more
suitable nest sites are unavailable. However, adding artificial nest
and perch sites in grasslands may encourage the use of grasslands by
woodland and edge species at the expense of raptors that primary use
grasslands [4].

Urban Settings: Wintering great horned owl density reflects
availability of medium-sized prey such as skunks, domestic cats, etc. [10].

Mortality: Major causes of death for great horned owls include
collisions with vehicles, shooting, and starvation [24,32]. The highest
mortality rates are among juveniles, largely due to cannibalism and
severe weather; annual mortality rate was 15 percent for nestlings, 58
percent for juveniles, 44 percent for 1- to 2-year-olds, and 28 percent
for adults over 2 years old [24,25]. At least 52 percent of banded and
recovered great horned owls had been shot and 12 percent had been
trapped; perhaps as many as 96 percent had been killed intentionally
[24]. Mortality due to pesticides during 1946 to 1968 was minimal [32];
however, poisoning of great horned owls due to pesticides used in urban
and suburban environments has been increasing [12].

Nuisance: The majority of respondents to a raptor nuisance survey
(33/54) reported great horned owl nuisance, damage, or safety problems.
Most reported problems involved predation at poultry and game farms, and
at beagle clubs (preying on domestic rabbits kept for club activities).
Other nuisance problems involved predation on pets including exotic
animals and birds [21].

Raptor Reintroduction Projects: Great horned owl presence at peregrine
falcon (Falco peregrinus) release sites is detrimental to the survival
of nestling and juvenile peregrine falcons. Great horned owls occupy
suitable peregrine falcon nest sites (which are usually scarce) and prey
on juvenile great horned owls. Much debate has occurred over the
feasibility and necessity for great horned owl removal during peregrine
falcon reestablishment. The intent of most great horned owl removal
have been to reduce the threat to young peregrine falcons immediately
after release. Personnel at the U.S. Fish and Wildlife Service have
stated that great horned owl control is unnecessary once falcons are
established and reproducing (with naturally fledged peregrine falcons
present). They do, however, support localized great horned owl control
for a few months after peregrine falcon release and/or fledging [22].
Similar problems pertain to prairie falcon (F. mexicanus) management;
most nest sites large enough for prairie falcons are also suitable for
great horned owls, and young prairie lafcons are vulnerable to predation
by great horned owls [30].


REFERENCES :
NO-ENTRY
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cc-publicdomain
библиографски навод
Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Occurrence in North America ( англиски )

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AL
AK
AZ
AR
CA
CO
CT
DE
FL
GA

ID
IL
IN
IA
KS
KY
LA
ME
MD
MA

MI
MN
MS
MO
MT
NE
NV
NH
NJ
NM

NY
NC
ND
OH
OK
OR
PA
RI
SC
SD

TN
TX
UT
VT
VA
WA
WV
WI
WY
DC





AB
BC
MB
NB
NF
NT
NS
ON
PE
PQ
SK
YT

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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Predators ( англиски )

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More info for the term: natural

Adult great horned owls have no natural routine predators. Antagonistic
interactions with red-tailed hawks and crows are common [25]. Crows mob
and harass great horned owls during the day; great horned owls attack
roosting groups of crows at night, killing many at a time [12].
лиценца
cc-publicdomain
библиографски навод
Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Preferred Habitat ( англиски )

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More info for the terms: density, frequency, grassland, shrub, tree

Great horned owls occupy more diverse habitats than any other owl;
habitats harboring great horned owls include deep forests (both
coniferous and deciduous), open woodlands, chaparral, desert cliffs,
woodlots, and wooded urban environments [12,32]. Great horned owls
prefer mature successional stages with openings [32]. Great horned owl
habitat usually includes fields and/or wetlands. Recent findings
suggest a lower density of great horned owls in heavily forested tracts
than in more open areas; for example, there is a lower frequency of
great horned owls in the heavily wooded northern third of Wisconsin than
in the more open southern two-thirds [32]. In Utah great horned owls
were found most frequently in thinned stands. They often forage in
slash piles [43]. In Maryland great horned owls are found in forests
and woodlots, adjacent fields, and marshes [38]. In New Jersey great
horned owls avoid close contact with human habitation and prefer to be
near water courses and in upland and lowland hardwoods. In southeastern
Wisconsin, an average of 27 percent of the entire annual home range was
wooded or in marshlands and wet shrub communities; the remainder varied
among open areas and agricultural developments. Actual usage patterns
within home ranges were concentrated in areas with appropriate hunting
and nesting sites (i. e., perches near open areas) [31,32]. The great
horned owl is found from sea level to timberline [13,37].

Home Range: In southeastern Wisconsin the average size of the great
horned owl's annual home range was about 813 acres (329 ha). Home
ranges of successful breeders were larger. Home ranges decreased for
both successful and unsuccessful breeders in spring as prey availability
increased. During summer, home ranges gradually expanded again [31].
Petersen [31] reported a density of one pair per 3 square miles (7.5 sq
km) in southeastern Wisconsin, but an active breeding density of one
pair per 4 square miles (9.3 sq km). Nesting densities of great horned
owls in Michigan ranged from 0.15 to 0.26 bird per square kilometer.
The average home range was 524 acres (212 ha) [9]. In eastern South
Dakota the daily range of great horned owls exceeded observation plot
size of 100 acres (40 ha) [16].

Roosting: Great horned owls usually roost in dense foliage, tree
cavities, old nests, and crevices in rocks [12].

Nesting: Nest sites are often chosen adjacent to open areas suitable
for hunting lagomorphs (Leporidae) and rodents (Rodentia) [13]. In
western grasslands, great horned owls were observed in four habitats:
unbroken grassland, creek bottoms, cliffs, and cultivated land. The
majority of great horned owl observations (80.5%) occurred in creek
bottoms [30]. Riparian areas are preferred for nest sites in the
northeastern states [28]. Supporting substrates for great horned owl
nests included trees (85%), cliffs (9.8%), and creekbanks (4.9%) [30].
In southeastern Wisconsin the number of active breeding pairs of great
horned owls was apparently related to cottontail (Silvilagus spp.)
density; owl productivity (number of young fledged) was positively
related to abundance of staple prey [31].

Hunting: Prey availability in grasslands is a function of prey density,
vegetation structure, and mode of hunting. Raptors tend to hunt in
areas with high capture probability [4]. In northeastern Colorado great
horned owls were observed in grazed bottomlands more often than in
ungrazed bottomlands, possibly because the lower vegetation left prey
more vulnerable [11]. Sympatry with common barn owls (Tyto alba) is
made possible by differing hunting strategies; for example, great horned
owls tend to hunt from perches and common barn owls typically capture
prey during flight [23].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Regional Distribution in the Western United States ( англиски )

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More info on this topic.

This species can be found in the following regions of the western United States (according to the Bureau of Land Management classification of Physiographic Regions of the western United States):

1 Northern Pacific Border
2 Cascade Mountains
3 Southern Pacific Border
4 Sierra Mountains
5 Columbia Plateau
6 Upper Basin and Range
7 Lower Basin and Range
8 Northern Rocky Mountains
9 Middle Rocky Mountains
10 Wyoming Basin
11 Southern Rocky Mountains
12 Colorado Plateau
13 Rocky Mountain Piedmont
14 Great Plains
15 Black Hills Uplift
16 Upper Missouri Basin and Broken Lands
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Taxonomy ( англиски )

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More info for the term: tundra

The currently accepted scientific name of great horned owl is Bubo
virginianus (Gmelin) [38]. The widespread yet sedentary nature of the
great horned owl has given rise to a number of races and subspecies,
probably due to lack of interbreeding. Accepted subspecies and their
common names are as follows [2,24,25]:

Bubo virginianus ssp. virginianus (Gmelin), great horned owl
B. v. ssp. algistus (Oberholser), St. Michael horned owl
B. v. ssp. heterocnemis (Oberholser), Labrador horned owl
B. v. ssp. lagophonus (Oberholser), northwestern horned owl
B. v. ssp. occidentalis Stone, Montana horned owl
B. v. ssp. pacificus Cassin, Pacific horned owl
B. v. ssp. pallascens Stone, western horned owl
B. v. ssp. saturatus Ridgway, dusky horned owl
B. v. ssp. scalariventris Snyder, Ontario horned owl
B. v. ssp. subarcticus (Hoy), arctic horned owl
B. v. ssp. wapacuthu (Gmelin), tundra horned owl
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Timing of Major Life History Events ( англиски )

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More info for the terms: altricial, formation

Migration: Great horned owls are resident in most parts of their range
in North America [32]. Most (93%) banded birds from a wide range of
study sites have been recovered within 48 miles (80 km) of the banding
location. Great horned owls banded in the South had traveled shorter
distances than great horned owls banded in the North [24]. Great horned
owls migrate away from conifer bogs and forests in the northern parts of
their range in severe winters. It is also common for great horned owls
to move from Canada to the northern Great Lakes States in winter [32].

Pair Formation: Great horned owls are usually the earliest nesting
raptors. Pair formation occurs in early winter; the male chooses a nest
site and attempts to attract a female by copious vocalizations [24].

Nesting: In Maryland and the District of Columbia great horned owls
nest from late January to late May; extreme egg dates are January 27 and
April 12 [38]. The typical great horned owl clutch is two or three
eggs; clutch sizes range from one to six eggs. The male feeds the
female while she incubates the eggs. Incubation time is 25 to 30 days
[12].

Development of Young: Hatching dates usually occurs in mid-February.
The altricial young are downy, with eyes closed. Their eyes usually
open by 7 days. Hatchlings are brooded almost constantly by the female
for up to 3 weeks. The male parent guards the nest closely. Nestlings
often edge out of the nest by about 32 days but remain near the nest and
continue to be cared for by the parents until after full flight is
achieved. At about 6 weeks of age nestlings begin flapping and learning
to fly; first flight may occur by 9 weeks but sustained flight is
usually not achieved until about 12 weeks. Fledglings may spend up to
14 days on the ground prior to achieving full flight capability [12,25].

Age at First Breeding: The great horned owl usually first breeds at
2 years of age [25].

Diurnal Activity: In Manitoba juvenile great horned owls were observed
hunting between 8 p.m. and 12 a.m. in July and August [7].

Longevity: The oldest banded great horned owl recovered in the wild was
13 years old. Captive birds may live more than 20 years [25].
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Use of Fire in Population Management ( англиски )

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More info for the terms: fire exclusion, fire regime, fire-free interval, prescribed fire, presettlement fire regime

Great horned owls use but are not limited to the following fire
dependent ecosystems:

Presettlement Fire Regime
______________________________________________________________
Habitat Average Fire-Free Interval

grasslands 1-5 years
semidesert grass-shrub up to 10 years
sagebrush (Artemisia spp.)-grass 20-100 years
chaparral 20-40 years
pinyon-juniper 10-30 years
ponderosa pine (Pinus ponderosa) 5-10 years
Douglas-fir (Pseudotsuga menziesii) 100-500 years
redwood (Sequoia sempervirens) 17-82 years
giant sequoia (Sequoiadendron gigantea) 5-10 years

Fire exclusion has had more detrimental effects than benefits on raptor
habitat. Prescribed fire in raptor habitats usually does not conflict
with raptor habitat objectives and can in many cases be beneficial [29].

FIRE REGIMES :
Find fire regime information for the plant communities in which this
species may occur by entering the species name in the FEIS home page under
"Find FIRE REGIMES".
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Sullivan, Janet. 1995. Bubo virginianus. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Available: http://www.fs.fed.us/database/feis/
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Distribution ( шпански; кастиљски )

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Chile Central
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Habitat ( шпански; кастиљски )

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Viven en sabanas con parches de arboles, cafetales, potreros con setos densos dispersos y cercas vivas.

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Behavior ( шпански; кастиљски )

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Son nocturnas y durante el día duermen en arboles densos. sobre todo en las filas de cipreses altos que bordean muchos potreros de las zonas altas.

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Distribution ( шпански; кастиљски )

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Distribucion en Costa Rica: Es una especie residente muy rara, sobre todo en el Valle Central. Hay observaciones recientes cerca de Ochomogo arriba de Cartago y cerca de Alajuela. Hay una observación cerca de Tabaga, Cañas (Guanacaste).


Distribucion General: Se encuentra desde Alaska y el norte de Canadá hasta la Tierra del Fuego.

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Trophic Strategy ( шпански; кастиљски )

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Cazan sobre todo en pastizales, sabanas, bordes de arboledas. Se alimentan de "zorros pelones" pequeños, y otros mamíferos de tamaño mediano y aves.

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Diagnostic Description ( шпански; кастиљски )

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53 cm.; 1 kg.. Es una ave muy grande, fuerte, con "orejas" conspícuas, la región inferior es barreteada y las patas son totalmente emplumadas. El disco facial es de color canela opáco con el borde negro, la región superior es negruzca, con barras y vermiculaciones grises, bases de las plumas color leonado; la barbilla y la lista que atraviesa la parte de adelante del cuello, son blancas; la garganta tiene una mezcla de fusco y ante; la región inferior es entre blancuzca y leonada, con vermiculaciones fuscas y un barreteado negro denso; las plumas de las patas y los dedos son color ante. El iris es amarillo; el pico y las garras son negruzcas.

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Diagnostic Description ( шпански; кастиљски )

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Localidad del tipo: in omni Americ, etc. = Virginia.
Depositario del tipo:
Recolector del tipo:
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Conservation Status ( шпански; кастиљски )

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Es considerada como una especie amenazada de extinción, debido a la pérdida de su hábitat por la deforestación. Está protegida y regulada por la Ley de Conservación de la Vida Silvestre No. 7317, la Ley Orgánica del Ambiente No. 7554 y el decreto No. 26435-MINAE. Asimismo está incluída en el Apéndice ll del Convenio sobre el Comercio Internacional de Especies Amenazadas de Fauna y Flora Silvestre (CITES).

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Bubo virginianus ( астурски )

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El búho cornudu, búho real[2] o búho americanu[3] (Bubo virginianus) ye una especie d'ave estrixiforme de la familia de los búhos (Strigidae). Ye nocherniega, de plumaxe rayáu. Ye dacuando tamién llamáu búho real americanu.

Distribución y carauterístiques

Habita nel continente americanu, dende Tierra del Fueu hasta'l norte d'Estaos Xuníos. Ye consideráu como la especie de búho más grande d'América.

El so pesu varia ente los 650 g y hasta 1 kg na mayoría de les subespecies. Añera en oquedades de tueros, y puede poner de 2 a 3 güevos. Aliméntase de pequeños mamíferos, reptiles ya inclusive peces. Reproducióse en cautiverio. Utilizóse y síguese utilizando para cetrería.

Subespecies

  • B. v. virginianus (Gmelin, 1788)
  • B. v. nacurutu, (Vieillot, 1817): ñacurutú
  • B. v. subarcticus Güei, 1852
  • B. v. pacificus Cassin, 1854
  • B. v. saturatus Ridgway, 1877
  • B. v. nigrescens Berlepsch, 1884
  • B. v. pallescens Stone, 1897
  • B. v. mayensis (Nelson, 1901)
  • B. v. elachistus Brewster, 1902.
  • B. v. heterocnemis (Oberholser, 1904)
  • B. v. lagophonus (Oberholser, 1904).
  • B. v. magellanicus[4] (tucúquere o búho magallánico) clasificóse como la especie Bubo magellanicus.[5]
  • B. v. mesembrinus (Oberholser, 1904)

Referencies

  1. BirdLife International. «Bubo virginianus» (inglés). Llista Roxa d'especies amenazaes de la UICN 2015.2.
  2. «Institutu Nacional d'Ecoloxía».
  3. Bernis, F; De Juana, E; Del Hoyo, J; Fernández-Cruz, M; Ferrer, X; Sáez-Royuela, R; Sargatal, J (2000). «Nomes en castellán de les aves del mundu recomendaos pola Sociedá Española d'Ornitoloxía (Quinta parte: Strixiformes, Caprimulxiformes y Apodiformes)». Ardeola. Handbook of the Birds of the World (Madrid: SEO/BirdLife) 47 (1): pp. 123-130. ISSN 0570-7358. http://www.seo.org/wp-content/uploads/tmp/docs/vol_47_1_quinto.pdf. Consultáu'l .
  4. ZipCodeZoo.com, Bubo virginianus magellanicus
  5. Aves de Chile.cl Tucúquere

Enllaces esternos

Protonotaria-citrea-002 edit.jpg Esta páxina forma parte del wikiproyeutu Aves, un esfuerciu collaborativu col fin d'ameyorar y organizar tolos conteníos rellacionaos con esti tema. Visita la páxina d'alderique del proyeutu pa collaborar y facer entrugues o suxerencies.
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Bubo virginianus: Brief Summary ( астурски )

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Bubo virginianus

El búho cornudu, búho real o búho americanu (Bubo virginianus) ye una especie d'ave estrixiforme de la familia de los búhos (Strigidae). Ye nocherniega, de plumaxe rayáu. Ye dacuando tamién llamáu búho real americanu.

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Toud-Virginia ( бретонски )

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An toud-Virginia a zo un evn-preizh, Bubo virginianus an anv skiantel anezhañ.

Doareoù pennañ

Boued

Annez

 src=
Tiriad an toud-Virginia.


Rummatadur

Liammoù diavaez


Commons
Muioc'h a restroù diwar-benn

a vo kavet e Wikimedia Commons.

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Toud-Virginia: Brief Summary ( бретонски )

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An toud-Virginia a zo un evn-preizh, Bubo virginianus an anv skiantel anezhañ.

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Duc americà ( каталонски; валенсиски )

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El duc americà,[1] duc reial[2] o duc banyut (Bubo virginianus) és una espècie d'au estrigiforme de la família dels Strigidae. És nocturn, de plomatge ratllat.

Distribució i característiques

Habita al continent americà, des de Terra del Foc fins al nord dels Estats Units. És considerat com a l'espècie de mussol més gran d'Amèrica.

El seu pes varia entre els 650 g i fins a 1 kg en la majoria de les subespècies. Nia en forats buits de troncs, i pot pondre de 2 a 3 ous. S'alimenta de petits mamífers, rèptils i fins i tot peixos. S'ha reproduït en captiveri. S'ha fet servir i es continua utilitzant per a falconeria.

Subespècies

  • B. v. virginianus (Gmelin, 1788)
  • B. v. nacurutu, (Vieillot, 1817): ñacurutú
  • B. v. subarcticus Hoy, 1852
  • B. v. pacificus Cassin, 1854
  • B. v. saturatus Ridgway, 1877
  • B. v. nigrescens Berlepsch, 1884
  • B. v. pallescens Stone, 1897
  • B. v. mayensis (Nelson, 1901)
  • B. v. elachistus Brewster, 1902.
  • B. v. heterocnemis (Oberholser, 1904)
  • B. v. lagophonus (Oberholser, 1904).
  • B. v. mesembrinus (Oberholser, 1904)

La subespècie B. v. magellanicus[3] (tucúquere o mussol magallànic) ara es classifica com a l'espècie B. magellanicus.[4]

Referències


Enllaços externs

 src= A Wikimedia Commons hi ha contingut multimèdia relatiu a: Duc americà Modifica l'enllaç a Wikidata  src= Podeu veure l'entrada corresponent a aquest tàxon, clade o naturalista dins el projecte Wikispecies.


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Duc americà: Brief Summary ( каталонски; валенсиски )

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El duc americà, duc reial o duc banyut (Bubo virginianus) és una espècie d'au estrigiforme de la família dels Strigidae. És nocturn, de plomatge ratllat.

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Tylluan gorniog fawr ( велшки )

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Aderyn a rhywogaeth o adar yw Tylluan gorniog fawr (sy'n enw benywaidd; enw lluosog: tylluanod corniog mawr) a adnabyddir hefyd gyda'i enw gwyddonol Bubo virginianus; yr enw Saesneg arno yw Great horned owl. Mae'n perthyn i deulu'r Tylluanod (Lladin: Strigidae) sydd yn urdd y Strigiformes.[1]

Talfyrir yr enw Lladin yn aml yn B. virginianus, sef enw'r rhywogaeth.[2] Mae'r rhywogaeth hon i'w chanfod yng Ngogledd America.

Teulu

Mae'r tylluan gorniog fawr yn perthyn i deulu'r Tylluanod (Lladin: Strigidae). Dyma rai o aelodau eraill y teulu:

Rhestr Wicidata:

rhywogaeth enw tacson delwedd Cordylluan Glaucidium passerinum Cordylluan Bolifia Glaucidium bolivianum
YungasPygmyOwl.jpg
Cordylluan Brasil Glaucidium brasilianum
Cactus Ferruginous Pygmy-owl.jpg
Cordylluan Ciwba Glaucidium siju
Cuban Pygmy-owl (Glaucidium siju).jpg
Cordylluan dorchog Glaucidium brodiei
Collared Owlet.jpg
Cordylluan fannog Glaucidium perlatum
Glaucidium perlatum (Etosha).jpg
Cordylluan frongoch Glaucidium tephronotum
GlaucidiumKeulemans.jpg
Cordylluan Hardy Glaucidium hardyi
Amazonian Pygmy-owl (Glaucidium hardyi) in tree.jpg
Cordylluan resog Asia Glaucidium cuculoides
Glaucidium cuculoides - Mae Wong.jpg
Cordylluan y goedwig Glaucidium radiatum
BarredJungleOwlet-2.jpg
Cordylluan y Gogledd Glaucidium gnoma
Mountain Pygmy Owl Glaucidium gnoma Arizona.jpg
Cordylluan yr Andes Glaucidium jardinii
Andean Pygmy-owl (Glaucidium jardinii) in tree.jpg
Diwedd y rhestr a gynhyrchwyd yn otomatig o Wicidata.

Gweler hefyd

Cyfeiriadau

  1. Gwefan Cymdeithas Edward Llwyd; adalwyd 30 Medi 2016.
  2. Gwefan Avibase; adalwyd 3 Hydref 2016.
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Tylluan gorniog fawr: Brief Summary ( велшки )

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Aderyn a rhywogaeth o adar yw Tylluan gorniog fawr (sy'n enw benywaidd; enw lluosog: tylluanod corniog mawr) a adnabyddir hefyd gyda'i enw gwyddonol Bubo virginianus; yr enw Saesneg arno yw Great horned owl. Mae'n perthyn i deulu'r Tylluanod (Lladin: Strigidae) sydd yn urdd y Strigiformes.

Talfyrir yr enw Lladin yn aml yn B. virginianus, sef enw'r rhywogaeth. Mae'r rhywogaeth hon i'w chanfod yng Ngogledd America.

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Výr virginský ( чешки )

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Výr virginský (Bubo virginianus) je statný a velký pták, jeden z mnoha zástupců rodu Bubo. Obývá severní, střední i Jižní Ameriku. Je to velice přizpůsobivý pták s velkým rozsahem rozšíření, ačkoli není v Americe tak rozšířený, jako sova pálená.

Výskyt

Většinu času tráví výr virginský na stromech v jehličnatých, listnatých i ve smíšených lesích, tropických deštných lesích, v prériích, pampách, hornatých oblastech, subarktických tundrách, pouštích, u skalnatých pobřeží a v některých městských oblastech. Ačkoli je jeho výskyt méně obvyklý ve více extrémních oblastech (tj. „srdce“ pouští, příliš husté deštné lesy, vysoké oblasti v arktických tundrách), obývá většinu lokalit v Americe.

Popis

Výr virginský dosahuje 46 až 68 cm na výšku, rozpětí křídel 101 až 153 cm a hmotnosti zhruba 1400 g. Obecně jsou největší sovy nejblíže u polárních oblastí a nejmenší sovy poblíž rovníku. Samice jsou o něco větší než samci. Dospělé sovy mají velké ušní chvostky, rudohnědou tvář a bílou skvrnu na hrdle. Vrchní část těla je kropenatá, spodek těla tvoří žlutohnědé svislé vlnkování. Ušní „chvostky“ tvoří pouze pera a nijak nesouvisí se sluchovým ústrojím. Mají skvělý sluch, který jim umožňuje nalézt přesné umístění jejich kořisti.

Potrava

Výr virginský na svou kořist číhá na vysokých stromech. Potrava tohoto výra je velice různorodá, ale žere převážně malé až střední savce, např. krysy, veverky, myši, krtky, skunky, rejsky, netopýry, lasice, ale také ptáky, hmyz, korýše, obojživelníky, plazy nebo ryby. Na vybraných území se stávají jeho důležitou součástí potravy i zajíci nebo králíci.

Chování

Dospělci vydávají čtyřslabičné, někdy pětislabičné „ho-ho-hoo hoo hoo“, mláďata většinou vydávají syčivé a prskavé zvuky.

Období páření se liší spolu s areálem rozšíření, může začínat už v lednu a únoru. Páry většinou využívají opuštěných hnízd od jiných druhů ptáků, někdy hnízdí v dutinách či na skalních útesech. Samice snese nejčastěji bílá 2-3 vejce, je-li dostatek potravy tak i 6, oba rodiče na nich sedí zhruba 35 dní.

Rozlišujeme u něj několik poddruhů:

  • B. v. virginianus (Gmelin, 1788)
  • B. v. nacurutu (Vieillot, 1817)
  • B. v. subarcticus Hoy, 1852
  • B. v. pacificus Cassin, 1854
  • B. v. saturatus Ridgway, 1877
  • B. v. nigrescens Berlepsch, 1884
  • B. v. pallescens Stone, 1897
  • B. v. mayensis (Nelson, 1901)
  • B. v. elachistus Brewster, 1902
  • B. v. heterocnemis (Oberholser, 1904)
  • B. v. lagophonus (Oberholser, 1904)
  • B. v. mesembrinus (Oberholser, 1904)

Galerie

Odkazy

Reference

  1. Červený seznam IUCN 2018.1. 5. července 2018. Dostupné online. [cit. 2018-08-09]

Externí odkazy

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Výr virginský: Brief Summary ( чешки )

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Výr virginský (Bubo virginianus) je statný a velký pták, jeden z mnoha zástupců rodu Bubo. Obývá severní, střední i Jižní Ameriku. Je to velice přizpůsobivý pták s velkým rozsahem rozšíření, ačkoli není v Americe tak rozšířený, jako sova pálená.

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Virginia-Uhu ( германски )

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 src=
Porträt eines Virginia-Uhus

Der Virginia-Uhu (Bubo virginianus) ist eine Vogelart aus der Gattung der Uhus (Bubo), die zur Familie der Eigentlichen Eulen (Strigidae) und zur Ordnung der Eulen (Strigiformes) gehört. Die Art ist in mehreren Unterarten über große Teile von Nord-, Mittel und Südamerika verbreitet. Der nah verwandte, in angrenzenden Regionen Südamerikas lebende Magellan-Uhu (Bubo magellanicus) wurde lange Zeit ebenfalls als eine Unterart des Virginia-Uhus angesehen.

Merkmale

Der Virginia-Uhu ist mit einer Länge von 46 bis 63 cm und Spannweite zwischen 91 und 151 cm eine der größten Eulenarten des amerikanischen Kontinents. Die Weibchen sind 10 bis 20 Prozent größer als die Männchen. Das Gewicht des Virginia-Uhus liegt bei 0,9 bis 1,8 kg. Die Gefiederfarbe variiert von grau bis rot-braun. Auf der Unterseite verlaufen dunkle Streifen längs seines Körpers sowie ein weißes Band auf der Brust. Der Bauch ist etwas heller als der Rücken. Er hat lange Ohren oder „Hörner“, die seinen englischen Namen Great Horned Owl erklären. Wie bei allen Uhus haben diese Federohren allerdings keine Bedeutung für den Gehörsinn. Die großen Augen sind gelblich orangefarben. Die Füße sind bis zu den Krallen befiedert.

Der Gesang des Männchens ist ein tiefes, weit klingendes bu-bubú booh booh, das in Intervallen von mehreren Sekunden wiederholt wird. Das Weibchen singt ähnlich, hat aber einen anderen Rhythmus und ruft bu-bububú booh.[1]

Lebensraum

Der Virginia-Uhu bevorzugt offene Landschaften mit Bäumen oder Waldrändern, aber auch bewaldete Gebirgsregionen bis 4000 m Höhe und sogar Parks.

Ernährung und Lebensweise

Der Virginia-Uhu ernährt sich überwiegend von Säugetieren, die bis zum Dreifachen seines eigenen Körpergewichts wiegen können, darunter Ratten, Mäuse, Kaninchen und Skunks, aber auch von Vögeln wie Tauben, Enten und anderen Eulen. Die Jagd findet dabei meist im Gleitflug statt, die Beute wird im Sturzflug mit angezogenen Flügeln geschlagen. Fische, Amphibien und kleine Alligatoren jagt er zum Teil auch auf dem Boden gehend und sogar im Wasser.

In Gefangenschaft können Virginia-Uhus über 30 Jahre alt werden, wild lebende Tiere leben selten mehr als 15 Jahre lang.

Stimme und Fortpflanzung

 src=
Drei junge Virginia-Uhus im Nest

Während der Paarungszeit im Januar und Februar lassen Männchen und Weibchen den typischen Ruf hu-hu huuh hu-hu hören. Die Stimme des Männchens ist tiefer als die des Weibchens.

Wie die meisten Uhus bauen Virginia-Uhus keine Nester, sondern benutzen gerne verlassene Greifvogelnester. Ihre Eier (zwei bis vier bei einem Gelege) werden innerhalb von 28 bis 35 Tagen ausgebrütet, wobei ausschließlich die Weibchen brüten. Die Jungtiere verlassen nach 6 bis 7 Wochen kletternd das Nest, nach 9 bis 10 Wochen sind die Jungtiere flügge.

Die Elternpaare teilen sich oft über viele Jahre dasselbe Territorium, leben allerdings außerhalb der Brutzeit solitär.

Verbreitung

 src=
Verbreitungsgebiet des Virginia-Uhus

Der Virginia-Uhu kommt in großen Teilen Nordamerikas außerhalb der Arktis sowie in einigen Regionen Mittel- und Südamerikas vor. Im südlichen Südamerika grenzt sein Verbreitungsgebiet an das des eng mit ihm verwandten Magellan-Uhus, der die Anden-Region bis Feuerland besiedelt. Die Art gilt laut IUCN als derzeit nicht gefährdet.[2]

Unterarten

Es werden folgende Unterarten unterschieden:

  • B. v. virginianus
  • B. v. lagophonus
  • B. v. algistus
  • B. v. saturatus
  • B. v. pacificus
  • B. v. elachistus
  • B. v. subarcticus
  • B. v. wapacuthu
  • B. v. occidentalis
  • B. v. arcticus
  • B. v. heterocnemis
  • B. v. scalariventris
  • B. v. mayensis
  • B. v. mesembrinus
  • B. v. pallescens
  • B. v. nigrescens
  • B. v. colombianus
  • B. v. nacurutu
  • B. v. scotinus
  • B. v. elutus
  • B. v. icelus
  • B. v. neochorus
  • B. v. deserti

Belege

Einzelbelege

  1. König et al., S. 319
  2. Bubo virginianus . BirdLife International, abgerufen am 16. Februar 2016 (englisch).

Literatur

Weblinks

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Virginia-Uhu: Brief Summary ( германски )

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 src= Porträt eines Virginia-Uhus

Der Virginia-Uhu (Bubo virginianus) ist eine Vogelart aus der Gattung der Uhus (Bubo), die zur Familie der Eigentlichen Eulen (Strigidae) und zur Ordnung der Eulen (Strigiformes) gehört. Die Art ist in mehreren Unterarten über große Teile von Nord-, Mittel und Südamerika verbreitet. Der nah verwandte, in angrenzenden Regionen Südamerikas lebende Magellan-Uhu (Bubo magellanicus) wurde lange Zeit ebenfalls als eine Unterart des Virginia-Uhus angesehen.

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பெரிய கொம்பு ஆந்தை ( тамилски )

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பெரிய கொம்பு ஆந்தை (great horned owl) என்பது ஆந்தை வகைகளில் ஒரு பறவையாகும். இவ்வாந்தை பெரிய அளவுள்ளது. கள்ளப்பருந்தைவிடக் கனமான பறவையாகும்.

விளக்கம்

பெரிய கொம்பு ஆந்தை கருந்தவிட்டு நிறமுடையது. மேனியில் கருங்கோடுகள் நீள்வட்டமாக காணப்படும். இரு கொம்புகள் போல கரு நிற இறகுகள் காதுக்கு மேலே உயர்ந்து இருக்கும்.

மேற்கோள்கள்

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பெரிய கொம்பு ஆந்தை: Brief Summary ( тамилски )

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பெரிய கொம்பு ஆந்தை (great horned owl) என்பது ஆந்தை வகைகளில் ஒரு பறவையாகும். இவ்வாந்தை பெரிய அளவுள்ளது. கள்ளப்பருந்தைவிடக் கனமான பறவையாகும்.

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Ma'xeméstaa'e

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Ma'xeméstaa'e, ve'kêseho-éve.

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Great horned owl ( англиски )

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The great horned owl (Bubo virginianus), also known as the tiger owl (originally derived from early naturalists' description as the "winged tiger" or "tiger of the air"),[3] or the hoot owl,[4] is a large owl native to the Americas. It is an extremely adaptable bird with a vast range and is the most widely distributed true owl in the Americas.[5] Its primary diet is rabbits and hares, rats and mice, and voles, although it freely hunts any animal it can overtake, including rodents and other small mammals, larger mid-sized mammals, birds, reptiles, amphibians, and invertebrates. In ornithological study, the great horned owl is often compared to the Eurasian eagle-owl (Bubo bubo), a closely related species, which despite the latter's notably larger size, occupies the same ecological niche in Eurasia, and the red-tailed hawk (Buteo jamaicensis), with which it often shares similar habitat, prey, and nesting habits by day, thus is something of a diurnal ecological equivalent.[6] The great horned owl is one of the earliest nesting birds in North America, often laying eggs weeks or even months before other raptorial birds.[7]

Taxonomy

The great horned owl was formally described in 1788 by the German naturalist Johann Friedrich Gmelin in his revised and expanded edition of Carl Linnaeus's Systema Naturae. He placed it with the other owls in the genus Strix and coined the binomial name Strix virginia.[8] Gmelin based his description on that of English naturalist George Edwards who had described and illustrated the great horned owl in 1747 in the second volume of his A Natural History of Uncommon Birds. Edwards had seen a live specimen from Virginia at the house of the Earl of Burlington in Chiswick. Edwards also owned a preserved specimen, and another specimen formed part of the Leverian collection.[9] The great horned owl is now placed in the genus Bubo that was introduced in 1805 by André Duméril.[10][11]

The great horned owl represents one of the one or two radiations of the genus across the Bering land bridge to the Americas. Whereas the Magellanic horned owl clearly divided once the owl had spread through the Americas, the consensus seems to be that the snowy owl and the great horned owl divided back in Eurasia and the snowy then spread back over the Arctic through northernmost North America separately from the radiation of the horned owl.[12][13] The great horned and Eurasian eagle-owls may in fact be conspecifics, based on similarities in life history, geographic distribution, and appearance.[6] In one case, a zoo-kept male great horned owl and female Eurasian eagle-owl produced an apparently healthy hybrid.[14] Genetic testing indicates that the snowy owl, not the Eurasian eagle-owl, is the most closely related living species.[12] Pleistocene era fossils have been found of Bubo owls in North America, which may either be distinct species or paleosubspecies, from as far east as Georgia, but predominantly in the Rocky Mountains and to the west of them.[15][16] Almost all fossils indicate these owls were larger than modern great horned owls.[17][18]

A large number of subspecies, more than 20 altogether, have been named. However, many of these are not true subspecies and only examples of individual or clinal variation. Subspecies differences are mainly in color and size and generally follow Gloger's and Bergmann's rules:[15] The most conservative treatments of great horned owl subspecies may describe as few as 10,[12] although an intermediate number is typical in most writings.[15]

Fifteen subspecies are currently recognised:[11]

  • B. v. algistus (Oberholser, 1904) – west Alaska
  • B. v. lagophonus (Oberholser, 1904) – central Alaska to northeast Oregon, Idaho and northwest Montana (USA)
  • B. v. saturatus Ridgway, 1877 – coastal southeast Alaska to coastal north California (USA)
  • B. v. pacificus Cassin, 1854 – coastal central California (USA) to northwest Baja California (Mexico)
  • B. v. subarcticus Hoy, PR, 1853 – central west Canada to north Idaho (USA)
  • B. v. pallescens Stone, 1897 – southwest USA to south Mexico
  • B. v. pinorum Dickerman & Johnson, AB, 2008 – south Idaho to north Arizona and north New Mexico (USA)
  • B. v. heterocnemis (Oberholser, 1904) – northeast Canada to the Great Lakes region
  • B. v. virginianus (Gmelin, JF, 1788) – southeast Canada to central, east USA
  • B. v. elachistus Brewster, 1902 – south Baja California (Mexico)
  • B. v. mayensis Nelson, 1901 – Yucatán Peninsula (southeast Mexico)
  • B. v. mesembrinus (Oberholser, 1904) – south Mexico to west Panama
  • B. v. nigrescens Berlepsch, 1884 – Colombia to northwest Peru
  • B. v. nacurutu (Vieillot, 1817) – east Colombia through the Guianas to north, east Brazil, Argentina, Bolivia and central Peru
  • B. v. deserti Reiser, 1905 – northeast Brazil (central north Bahia)

Description

The great horned owl is generally colored for camouflage.[7] The underparts of the species are usually light with some brown horizontal barring; the upper parts and upper wings are generally a mottled brown usually bearing heavy, complex, darker markings. All subspecies are darkly barred to some extent along the sides, as well.

Great horned owl showing much of its camouflage pattern/color

A variable-sized white patch is seen on the throat. The white throat may continue as a streak running down the middle of the breast even when the birds are not displaying, which in particularly pale individuals can widen at the belly into a large white area. South American great horned owls typically have a smaller white throat patch, often unseen unless actively displaying, and rarely display the white area on the chest.[6] Individual and regional variations in overall color occur, with birds from the subarctic showing a washed-out, light-buff color, while those from the Pacific Coast of North America, Central America, and much of South America can be a dark brownish color overlaid with blackish blotching. The skin of the feet and legs, though almost entirely obscured by feathers, is black. Even tropical great horned owls have feathered legs and feet. The feathers on the feet of the great horned owl are the second-longest known in any owl (after the snowy owl).[6] The bill is dark gunmetal-gray, as are the talons.[12]

All great horned owls have a facial disc. This can be reddish, brown, or gray in color (depending on geographical and racial variation) and is demarked by a dark rim culminating in bold, blackish side brackets.[19] This species' "horns" are tufts of feathers, called plumicorns. The purpose of plumicorns is not fully understood, but the hypothesis that they serve as a visual cue in territorial and sociosexual interactions with other owls is generally accepted.[6]

Physiology and measurements

The eyes of great horned owls are among the largest of terrestrial vertebrates.

The great horned owl is the heaviest extant owl in Central and South America and is the second-heaviest owl in North America, after the closely related, but very different-looking snowy owl.[7][12] It is heavily built, with a barrel-shaped body, a large head, and broad wings.[12] Its size can vary considerably across its range, with populations in interior Alaska and Ontario being largest and populations in California and Texas being smallest, though those from the Yucatán Peninsula and Baja California appear to be even smaller.[20][21] Adult great horned owls range in length from 43 to 64 cm (17 to 25 in), with an average of 55 cm (22 in), and possess a wingspan of 91 to 153 cm (3 ft 0 in to 5 ft 0 in), with an average of 122 cm (48 in). Females are somewhat larger than males.[15][22] Mean body weight is 1,608 g (3.545 lb) for females and 1,224 g (2.698 lb) for males.[23][24] Depending on subspecies, maximum weight can reach 2,503 g (5.518 lb).[25]

Great horned owl wings

The wing chord length is 297–400 mm (11.7–15.7 in).[26] The wing loading, the measured wing area compared to weight, is high, meaning the wings are relatively small in surface area for the bird's weight; the species' wing loading has been described as proportionately the highest among raptors.[19][27] The tail, being relatively short as is typical of most owls, is 175 to 252 mm (6.9 to 9.9 in) long. Like other owl species, the great horned owl is capable of “silent flight”, which is the way owls fly while making almost no discernable noise, despite their large size. This is made possible thanks to three main components of the owl's wing structure. The leading edge of their feathers have serrations that help to disrupt the turbulence generated by wing flapping, then the softer feathers help deaden the sound, and finally the trailing fringe of the feathers that works to finish cutting the sounds made by flight. The structure of the great horned owl wing also allows it to fly at a very low speeds for the size of the species, as slow as 2 miles per hour when they are gliding on breezes.[28]

Great horned owl (Canada)

The legs, feet, and talons are large and powerful. Tarsal length is 54–80 mm (2.1–3.1 in).[12] The average foot span of a fully spread foot, from talon to talon, is around 20 cm (7.9 in), as compared to 8 cm (3.1 in) in long-eared owls, 13 to 15 cm (5.1 to 5.9 in) in barn owls, and 18 cm (7.1 in) in the great grey owl.[6][29] Great horned owls can apply at least 300 lb/in2 of crushing power in their talons, a pressure considerably greater than the human hand is capable of exerting. In some big females, the gripping power of the great horned owl may be comparable to much larger raptor species such as the golden eagle.[30]

The hard, inflexible bill of the great horned owl is 3.3–5.2 cm (1.3–2.0 in) long, although the culmen, the exposed bill portion as measured along the top of the beak, is only 2.1 to 3.3 cm (0.83 to 1.30 in).[31]

The outer ear openings, which are concealed by feathers on the sides of the head, are relatively smaller than those of the Eurasian eagle owl, being 2.3 cm (0.91 in) in vertical axis, with the left ear slightly larger than the right.[32] Like most exclusively (or near exclusively) nocturnal species, the great horned owl has asymmetrical ear holes that allow for the triangulation of sounds when hunting in the dark. The different-height holes, while still close together, are differentiated enough that the owl is able to use the timing and direction of the sound waves hitting each hole to precisely locate prey even if the prey is located under cover such as snow. The disc-like shape of their faces also helps to direct the sounds they hear toward their ears. While the true nature/purpose of the ear tufts that are present on the great horned owl is unknown, researchers agree that the tufts do not play any role in the hearing ability of the owl. It is estimated that their hearing is up to ten times that of a human being.[33]

The great horned owl's eyes, just slightly smaller than the eyes of a human being, are large even for an owl and rank proportionately among the largest eyes of all terrestrial vertebrates.[34] The great horned owl has cylindrical eyes which creates more distance from the lens of the eye to the retina, which allows it to act more like a telephoto lens for farther distance sight compared to that possible from round eyes.[35] They are visually highly adapted for nocturnal hunting and provide a wide, almost completely binocular field of view, a large corneal surface and a predominantly rod retina.[36] The great horned owl's eye contains both rods and cones like most species that see in color, but the vision of a great horned owl closely resembles that of many other nocturnal species. The peak wavelengths that are observed by the cones is 555 nm and the research suggests that the great horned owl has relatively weak color vision, especially compared to other bird species. Despite (or perhaps as a result of) the poorer sense of color vision, the owl manages to have excellent night vision.[37] Instead of turning its eyes, an owl must turn its whole head, and the great horned owl can rotate its neck 270°. The iris is yellow, except in the amber-eyed South American great horned owl (B. v. nacurutu).

Calls

Audio great horned owl

The great horned owl's song is normally a low-pitched but loud ho-ho-hoo hoo hoo (or also transcribed as bu-bubu booh, who-hoo-ho-oo or who-ho-o-o, whoo-hoo-o-o, whoo) and can last for four or five syllables. The call is resonant and has warranted descriptions as varied as "solemn" and "terrifying".[6][7] The female's call is higher and rises in pitch at the end of the call. Female vocalizations are higher in pitch because of a smaller syrinx in the larger sex.[38] Calling seems to peak after rather than before midnight.[39][40] Usually, territorial hooting decreases in February or March at the onset of egg laying.[41] On occasion, this species exhibits "an indescribable assemblage of hoots, chuckles, screeches, and squawks, given so rapidly and disconnectedly that the effect is both startling and amusing".[42] Descriptions of some of these odd sounds including a growling krrooo-ooo note pair, a laughing whar, whah, wha-a-a-a-ah, a high-pitched ank, ank, ank; a weak, soft erk, erk, a cat-like meee-owwwwww, a hawk-like note of ke-yah, ke-yah, and a nighthawk-like peent. These vocalizations may be variously uttered when the birds are disturbed and angered at the nest (frequently preceding an attack on an interloping human or other animal), represent the vocal development of young owls, or are given during courtship and during territorial disputes with other owls.[7][15][43] Young owls still in the care of their parents make loud, persistent hissing or loud, piercing screeching sounds that are often confused with the calls of the barn owl.[12]

Subspecies

Coastal great horned owl (B. v. saturatus) at Grouse Mountain (North Vancouver, British Columbia)
South American great horned owl (B. v. nacurutu) with its notably dark eyes
Northern great horned owl (B. v. subarcticus) in Manitoba
California great horned owl (B. v. pacificus) stretching, Bernal Hill Park, San Francisco
Desert great horned owl (wet feathered) (B. v. pallescens) waiting out a rainstorm in the Mojave Desert
Mojave Desert, desert great horned owl (B. v. pallescens) on top of a Joshua tree in the summer of 2018

Common/eastern great horned owl (Bubo virginianus virginianus)

Eastern United States eastwards from at least as far west as Minnesota to Texas; northeastwards in distribution to southern Quebec, southern Ontario, Nova Scotia and Prince Edward Island. Resident all-year.[15] The race B. v. mesembrinus from Central America south of the Isthmus of Tehuantepec, may be merely a southerly leg of this race, as its coloring is almost exactly the same as virginianus, although with rather smaller body size. However, mesembrinus type owls are discontinuous in range, with only paler owls from pallescens and mayensis found in the in-between range before the northern virginianus reappears back up in South Texas.[12][21]
The "nominate race" is a medium-hued form, neither darkly saturated nor strikingly pale. Darker gray or somewhat paler individuals are known. It tends to be richly tinged with rufous and barred distinctly blackish-brown below with rather soft contrast. The feet can range from tawny to buff to creamy and are the legs are typically barred dark to a moderate extent. The facial disc is often a solid cinnamon-red color. This is mid-to-large race, with a wing chord length of 319–371 mm (12.6–14.6 in), averaging 339 mm (13.3 in), in males and 343–388 mm (13.5–15.3 in), averaging 362.8 mm (14.28 in), in females.[12][26][44] Unexpectedly, although it is not the longest-winged, the nominate is the heaviest known race as males weigh from 985 to 1,588 g (2.172 to 3.501 lb), averaging 1,318 g (2.906 lb), and females weigh from 1,417 to 2,503 g (3.124 to 5.518 lb), averaging 1,768.5 g (3.899 lb); the prior figures originally from a huge sample around Michigan. In comparison, B. v. subarcticus, though averaging longer in wing length averages somewhat less heavy.[23][26] On the contrary, in Costa Rica, within the range of the possibly synonymous mesembrinus, great horned owls average approximately 1,000 g (2.2 lb), the lightest average mass reported anywhere for this species.[45] Other standard measurements of this race are a tail length of 190 to 235 mm (7.5 to 9.3 in), a tarsus length of about 56 to 58 mm (2.2 to 2.3 in) and a bill length of 35 to 50 mm (1.4 to 2.0 in).[12][23][26][44] B. v. virginianus also tends to have relatively the longest ear tufts on any race.[19]

South American great horned owl (Bubo virginianus nacurutu)

A lowland form occurring in disjunct populations from eastern Colombia to the Guyanas; also from Brazil and Uruguay south of the Amazon Basin to Bolivia, the Buenos Aires Province in northern Argentina and western Paraguay; resident all-year. Includes the proposed subspecies scotinus, elutus, and deserti.[15][46][47] The status of this form, especially the relationships between the scattered subpopulations and with ssp. nigrescens and the Magellanic horned owl, deserves more study.
Dull, earthy brownish color is typical; birds from the semiarid interior of Brazil often have much white on uppertail- and ear-coverts against a dull gray background (sometimes separated as deserti). This race is less fuscous than nigrescens. It is the only subspecies where the iris is amber, not yellow. The Magellanic horned owl, while somewhat similar in coloring, has yellow eyes like other horned owls, not amber eyes. B. v. nacurutu is a medium-sized race, smaller than most in North America but not as small as some of the Mexican races. The wing chord length is 330–354 mm (13.0–13.9 in) in males and 340–376 mm (13.4–14.8 in) in females. The tail in both sexes can range from 184 to 217 mm (7.2 to 8.5 in). Only three birds have had published weights, two males scaling 1,011 and 1,132 g (2.229 and 2.496 lb) and one female weighing 1,050 g (2.31 lb). The most notable feature of this race is its large bill, at 43 to 52 mm (1.7 to 2.0 in), which is the biggest of any horned owl race despite the otherwise moderate size of B. v. nacurutu.[19][15][46]

Northern/sub-Arctic great horned owl (Bubo virginianus subarcticus)

Breeding range from Mackenzie, British Columbia region east to the southern Hudson Bay; southern limit unclear but at least reaches to Montana and North Dakota. Non-breeding birds are regularly found south to latitude 45°S, i.e. Wyoming or South Dakota, occasionally ranging beyond this limit especially in years with low prey in the north. This race includes the birds described as occidentalis (based on a wintering individual, as was the original subarcticus) and sclariventris.[48] The older name wapacuthu was occasionally used for this subspecies, but it cannot with certainty be assigned to a recognizable taxon and is thus considered a nomen dubium.[49] The population described as algistus is probably based on wandering individuals and/or various intergrades of subarcticus with other races.[15][50]
This is the palest form of horned owl, with the ground color essentially whitish with a faint buff tinge above; black underside barring variable from indistinct to pronounced, being most often prominent on the upper chest amongst otherwise pale plumage. This race shows little to no reddish coloration. B. v. subarcticus shows a very high degree of clinal variation, ranging from in the Contiguous United States where owls are often medium-grayish and more heavily marked to the subarctic zone in Canada where very pale birds with almost non-existent markings are prominent. Very pale birds are similar to a young female snowy owl from a distance. In this race, the feet range from immaculate white to buff, with little or no mottling.[12][15] In the west of Canada, subarcticus may hybridize with the dark saturatus and may do the same with this similarly dark heterocnemis in the east. In both cases, they may produce intermediate looking hybrids of reddish tone, like a virginianus but with sharper contrasting of colors.[51] This is one of the largest-bodied subspecies.[52] The wing chord length is 323–372 mm (12.7–14.6 in), averaging 346.7 mm (13.65 in), in males and 339–390 mm (13.3–15.4 in), averaging 362.5 mm (14.27 in), in females. Body mass ranges from 865 to 1,460 g (1.907 to 3.219 lb), averaging 1,196.5 g (2.638 lb), in males and from 1,112 to 2,046 g (2.452 to 4.511 lb), averaging 1,556 g (3.430 lb), in females. Tail length is 200 to 225 mm (7.9 to 8.9 in) and 220 to 240 mm (8.7 to 9.4 in) in males and females, respectively. Bill length is 35 to 43 mm (1.4 to 1.7 in) in both and one bird had a tarsus of 66 mm (2.6 in).[6][20][24][26][53][54]

California great horned owl (Bubo virginianus pacificus)

Central and southern California west of the Sierra Nevada except for the San Joaquin Valley, south to Northwestern Baja California, Mexico. Intergrades with pallescens in San Diego County, California (see also below). Resident all-year.[15]
Very rich brown, dark underside barring distinct, less pronounced than in saturatus but more pronounced than in pallescens. Humeral area is black. Feet are mottled dark. The facial disc is often even darkly mottled.[15] This is a fairly small-bodied race, in fact including the lightest wild great horned owl adult ever weighed. The wing chord length is 305–362 mm (12.0–14.3 in), averaging 332.5 mm (13.09 in), in males and 335–375 mm (13.2–14.8 in), averaging 351.4 mm (13.83 in), in females. Body mass ranges from 680 to 1,272 g (1.499 to 2.804 lb), averaging 991.7 g (2.186 lb), in males and from 825 to 1,668 g (1.819 to 3.677 lb), averaging 1,312.7 g (2.894 lb), in females. Tail length is 175 to 218 mm (6.9 to 8.6 in) and 203 to 230 mm (8.0 to 9.1 in) in males and females, respectively. Bill length is 34 to 41 mm (1.3 to 1.6 in) and one bird had a tarsus of 57 mm (2.2 in).[6][20][24][26]

Coastal great horned owl (Bubo virginianus saturatus)

Pacific coast from southeastern Alaska to northern California. Includes the previously described form of B. v. leucomelas. The often-recognized race B. v. lagophonus is often now considered a mere clinal variation of the same race from interior Alaska to Oregon, the Snake River, and northwestern Montana.[15][51] These forms may be reported in winter as far south as Colorado and Texas, but these are in times of irruption.[47]
A dark and overall brownish form with heavily barred and mottled underside, with a dull tawny base. Inland birds (lagophonus) tend to have a more grayish base, the coastal owls being more richly brown. Otherwise, inland and coastal owls are practically the same. The facial disc can range from gray to reddish-gray to dark rufous. The feet are fairly dusky gray typically, although some buff-footed individuals are known, and legs are more prominently barred with black than in other North American races.[12][15] This is a large race going on linear measurements, which in Alaskan owls outmatch those of all other races but for heterocnemis in Ontario (which may itself be a discontinuous eastern wing of this race). The wing chord length is 330–370 mm (13–15 in), averaging 348.3 mm (13.71 in), in males and 339–400 mm (13.3–15.7 in), averaging 374.7 mm (14.75 in), in females. Tail length is 191 to 245 mm (7.5 to 9.6 in) and 196 to 252 mm (7.7 to 9.9 in) in males and females. In both sexes, known bill and tarsal lengths are 35 to 44 mm (1.4 to 1.7 in) and 62 to 70 mm (2.4 to 2.8 in). No weights are known to have been published.[6][20][24][26]

North Andean great horned owl (Bubo virginianus nigrescens)

Andes; arid temperate and puna zones from Colombia to northwestern Peru. Resident all-year round. Presumably synonymous with the described columbianus.[12]
A dark, cold gray-brown form with heavy fuscous blotching. Arguably this is the darkest colored race on average, though it could be rivaled by individuals from saturatus and elachistus. This race has only minimally the rufous tinge seen in other darkish races, although some nigrescens may have a cinnamon facial disc.[12] The largest winged race of owl in South America, this owl has a wing chord length of 345–365 mm (13.6–14.4 in) in males and 350–382 mm (13.8–15.0 in) in females. The tail in both sexes can range from 185 to 217 mm (7.3 to 8.5 in). Bill length is 40 to 50 mm (1.6 to 2.0 in), again relatively long as in nacurutu and one bird had a tarsal length of 80 mm (3.1 in), indicating relatively long legs in the race. No published weights are known.[6][46] Apparently, despite its sizeable wing area, nigrescens is notably smaller overall when specimens are compared side-by-side with those from saturatus.[12]

Desert great horned owl (Bubo virginianus pallescens)

San Joaquin Valley southeastwards through arid regions of southeastern California and southern Utah eastwards to western Kansas and southwards to Guerrero and western Veracruz in Mexico; intergrades with pacificus in San Diego County, if not elsewhere; vagrant individuals of saturatus and the Rocky Mountains population, which look similar to intergrades, also seem to occur in its range. Resident all-year.[15] This race is likely synonymous with melanocercus.[12]
A pale dusky buff form with indistinct barring, especially on the underside. Darker individuals tend to have a deeper fulvous base to their upper sides. Humeral area is umber in color and the feathers of the feet are white and usually unmarked.[12] A small race, it averages slightly larger in wing length than pacificus but weighs less on average. The wing chord length is 318–367 mm (12.5–14.4 in), averaging 337.2 mm (13.28 in), in males and 332–381 mm (13.1–15.0 in), averaging 348.9 mm (13.74 in), in females. Body mass ranges from 724 to 1,257 g (1.596 to 2.771 lb), averaging 914.2 g (2.015 lb), in males and from 801 to 1,550 g (1.766 to 3.417 lb), averaging 1,142.2 g (2.518 lb), in females. In both sexes, tail length is 190 to 235 mm (7.5 to 9.3 in) and bill length is 33 to 43 mm (1.3 to 1.7 in).[6][20][24][26]

Yucatán great horned owl (Bubo virginianus mayensis)

Endemic to the southern two-thirds of the Yucatán Peninsula. Resident all-year.
A medium-pale form, fairly similar to pallescens in both hue and ventral markings. Going on linear measurements, B. v. mayensis is smaller than all North American horned owls, even the smallish pallescens, and is only slightly larger at median than the following race.[6] This race has wing chord and tail lengths of 297–340 mm (11.7–13.4 in) and 180 to 198 mm (7.1 to 7.8 in) in males and 303–357 mm (11.9–14.1 in) and 199 to 210 mm (7.8 to 8.3 in) in females. In both sexes, the bill length is 39 to 41 mm (1.5 to 1.6 in) and tarsal length is 54 to 65 mm (2.1 to 2.6 in).[21]

Baja California great horned owl (Bubo virginianus elachistus)

Southern Baja California, Mexico. Resident all-year.
Similar in color to pacificus but even darker and more heavily barred, like a miniaturized saturatus. It is considerably (5–10%) smaller than pacificus linearly; some size overlap does occur though. On average, it is the smallest known subspecies. Males have a wing chord length of 305 to 335 mm (12.0 to 13.2 in), tail length of 175 to 206 mm (6.9 to 8.1 in) and bill length of 33 to 38 mm (1.3 to 1.5 in). A single female had a wing chord of 330 mm (13 in) and tail of 211 mm (8.3 in).[12][21]

Northeastern great horned owl (Bubo virginianus heterocnemis)

Breeds in eastern Canada (northern Quebec, Labrador, Newfoundland). Its southern breeding range seems to be delineated by the Saint Lawrence River.[51] In winter, this race may disperses southwards throughout Ontario to as far as the Northeastern United States. This subspecies may be synonymous with saturatus, although it is distributed far to the east of that race. B. v. heterocnemis is surrounded by the much paler subarcticus to its west and quite differently marked virginianus to its south, the latter two overlap and possibly hybridize in some of the northeast.[47]
A fairly dark and grey, heavily barred form. Feet pale with dusky mottling. Going on median reported linear measurements (since body mass is unknown), this is the largest bodied subspecies on average. Males have a wing chord length of 350 to 365 mm (13.8 to 14.4 in) and females range from 370 to 390 mm (15 to 15 in). In both sexes, the tail is 220 to 250 mm (8.7 to 9.8 in) and the bill is 38 to 48 mm (1.5 to 1.9 in).[6][15][51]

Rocky Mountains great horned owl (Bubo virginianus pinorum)

The Rocky Mountains population breeds south of the Snake River in Idaho south to Arizona, New Mexico, and the Guadalupe Mountains of Texas. Westwards, it is presumed to occur to the Modoc Plateau and Mono Lake of California. This race was included in the presumed subspecies occidentalis, but was recently first described and named as a distinct subspecies and makes up the missing piece in the once-muddled distribution of great horned owls in the West and Rockies. Downslope movements into valleys occupied by pallescens might occur, but this needs study.
A medium gray form, intermediate in coloring between saturatus and pallescens. Moderately barred and tinged buff or ochraceous on the underside. Feet mottled. This is a largish race, wing chord lengths being inexplicably greater in males, at 350 to 397 mm (13.8 to 15.6 in), than in females, at 327 to 367 mm (12.9 to 14.4 in). Tail length can range from 190 to 233 mm (7.5 to 9.2 in) and a female weighed 1,246 g (2.747 lb).[15][55]

Species identification

Illustrated comparison of a great horned owl, left, to its closest North American relative, the snowy owl

The combination of the species' bulk, prominent ear tufts and barred plumage distinguishes it through much of the range, but it may be easily confused with the lesser or Magellanic horned owl (B. magellanicus), which may overlap in range.[12] The Magellanic horned owl was once considered a subspecies of the great horned, but is now almost universally considered a distinct species, as is supported by genetic materials, with the great horned being the paraspecies.[12][19] Overall coloration is similar, but the Magellanic is markedly smaller with smaller feet and a smaller head, with finer, but more numerous brownish bars on the underside, rather than the blotchy, irregular barring typical of great horned owls.[12] Other eagle-owls may superficially be somewhat similar, but the species is generically allopatric with the exception of wintering snowy owls. More tropical species with ear tufts, the stygian owl (A. stygius) and striped owl (A. clamator), are much smaller.[12] Other large owls lack ear tufts.[6]

Desert great horned owl (B. v. pallescens) perched on the top of a Joshua tree in Landers, California

Distribution and habitat

A great horned owl in a barn, Ontario, Canada

The breeding habitat of the great horned owl extends high into the subarctic of North America, where they are found up to the northwestern and southern Mackenzie Mountains, Keewatin, Ontario, northern Manitoba, Fort Chimo in Ungava, Okak, Newfoundland and Labrador, Anticosti Island and Prince Edward Island. They are distributed throughout most of North America and very spottily in Central America and then down into South America south to upland regions of Argentina, Bolivia and Peru, before they give way to the Magellanic horned owl, which thence ranges all the way to Tierra del Fuego, the southern tip of the continent. It is absent or rare from southern Guatemala, El Salvador, Nicaragua, and Costa Rica to Panama (where only two records) in Central America and the mangrove forests of northwestern South America. The species is also absent from the West Indies, the Haida Gwaii and almost all off-shore islands in the Americas, its ability to colonize islands apparently being considerably less than those of barn owls and short-eared owls.[6][45][47][56][57] Since the division into two species, the great horned owl is the second most widely distributed owl in the Americas, just after the barn owl.[12]

The great horned owl is among the world's most adaptable owls or even bird species in terms of habitat. The great horned owl can take up residence in trees that border all manner of deciduous, coniferous, and mixed forests, tropical rainforests, pampas, prairie, mountainous areas, deserts, subarctic tundra, rocky coasts, mangrove swamp forests, and some urban areas.[12] It is less common in the more extreme areas of the Americas. In the Mojave and Sonora Deserts, they are absent from the heart of the deserts and are only found on the vegetated or rocky fringes. Even in North America, they are rare in landscapes including more than 70% old-growth forest, such as the aspen forest of the Rockies.[15][58] They have only been recorded a handful of times in true rainforests such as the Amazon rainforest.[6] In the Appalachian Mountains, they appear to use old-growth forest[59] but in Arkansas are actually often found near temporary agricultural openings in the midst of large areas of woodland.[60] Similarly in south-central Pennsylvania, the owls use cropland and pasture more than deciduous and total forest cover, indicating preference for fragmented landscapes.[61] In prairies, grasslands and deserts, they can successfully live year round as long as there are rocky canyons, steep gullies and/or wooded coulees with shade-giving trees to provide them shelter and nesting sites.[6][62]

In mountainous areas of North America, they are usually absent above the tree line, but great horned owls can be found up to 2,100 m (6,900 ft) in California and 3,300 m (10,800 ft) in the Rockies.[6][63] In the Andean Mountains, on the other hand, they have adapted to being a true montane species, often found at least 3,300 m (10,800 ft) above sea level and are regularly recorded in treeless Puna grassland zones at 4,100 to 4,500 m (13,500 to 14,800 ft) in Ecuador and Peru.[64] They are generally rare in non-tidal wetland habitat,[65] and are replaced in the high Arctic tundra by snowy owls.[12] They prefer areas where open habitats, which they often hunt in, and woods, where they tend to roost and nest, are juxtaposed.[40][66][67] Thus lightly populated rural regions can be ideal. This species can occasionally be found in urban or suburban areas. However, they seem to prefer areas with less human activity and are most likely to be found in park-like settings in such developed areas, unlike eastern and western screech owls (Megascops asio & M. kennicottii) which may regularly occur in busy suburban settings. All mated great horned owls are permanent residents of their territories, but unmated and younger birds move freely in search of company and a territory, and leave regions with little food in winter.[12]

Behavior

Composite photo of great horned owl flight phases
Great horned owls are typically sluggish and passive but aware during daytime.

In most aspects of their behavior, great horned owls are typical of owls and most birds of prey. From experimentally raising young owls in captivity, Paul L. Errington felt that they were a bird of "essentially low intelligence" that could only hunt when partially wild and instinctually driven by hunger to hunt whatever they first encounter. He showed captive birds that were provided strips of meat from hatching, rather than having to hunt or to simulate hunting to obtain food, had no capacity to hunt.[68] On the contrary, William J. Baerg compared behaviorally his captive-raised great horned owls to parrots, which are famously intelligent birds, although not as often playful "it knows its keeper and usually accepts whatever he wishes to do with a good deal of tolerance".[69]

Arthur C. Bent also noted the variability in temperaments of great horned owls to their handlers, some generally pleasant, though most are eventually aggressive.[7] Most captive specimens, once mature, seem to resent attempts at contact and are often given to attacking their keepers. They will only follow cues when conditioned from an early age but rarely with the same level of success seen in some diurnal birds of prey trained for falconry or entertainment, although this does not necessarily correlate with intelligence as posited by Errington.[68][69] Carl D. Marti also disagrees with Errington's assessments, noting that their prey selection is not as "completely random as Errington suggested"; while "Great Horned Owls appeared to select their mammalian prey in general relation to the prey populations. Cottontails, however, appeared to be selected as prey out of relation to their population status".[29]

Like most owls, the great horned owl makes great use of secrecy and stealth. Due to its natural-colored plumage, it is well camouflaged both while active at night and while roosting during the day. During the daytime it roosts usually in large trees (including snags & large hollows but usually thick branches) but may occasionally be in crevices or small caves in rocks or in dense shrubbery. Pine and other coniferous trees may be preferred where available since they are particularly dense and provide cover throughout the year. Typically, males have a favorite roosting site not far from the nest, sometimes used over successive years.[4] While roosting, great horned owls may rest in the "tall-thin" position, where they sit as erect and hold themselves as slim as is possible. The kind of posture is well known as a further method of camouflage for other owls, like long-eared owls or great grey owls, especially if humans or other potential mammalian carnivores approach them. The Eurasian eagle owl rarely, if ever, assumes the tall-thin position.[70]

Outside of the nesting season, great horned owls may roost wherever their foraging path ends at dawn.[43] Generally great horned owls are active at night, although in some areas they may be active in the late afternoon or early morning. At dusk, the owl utters a few calls before flying to a more open sing-post, i.e. large bare branch or large rocks to deliver song. Normally several perches are used to mark occupied territory or to attract a female.[12] Despite its camouflage and cryptic locations, this species can still sometimes be spotted on its daytime roosts, especially by American crows (Corvus brachyrhynchos). Since owls are, next to red-tailed hawks, perhaps the main predator of crows and their young, crows sometimes congregate from considerable distances to mob owls and caw angrily at them for hours on end. When the owls try to fly off to avoid this harassment, they are often followed by the corvids.[71]

Territoriality and movements

Typically, great horned owls are highly sedentary, often capable of utilizing a single territory throughout their mature lives.[72] Although some species such as snowy owls, northern saw-whet owls, long-eared and short-eared owls are true migrants, most North American owls are not migratory and will generally show fidelity to a single territory year around.[6] In great horned owls, mated pairs occupy territories year-round and long-term. Territories are established and maintained through hooting, with highest activity before egg-laying and second peak in autumn when juveniles disperse, and can range from an average of 16 km2 (6.2 sq mi) in Yukon to an average of 2.1 km2 (0.81 sq mi) in Wyoming.[23][43]

Most territorial defense is performed by males, but females frequently assist their partners in hooting contests with neighbors or intruders, even during incubation.[15] On occasion, although territory borders may be successfully maintained via vocalizations alone without even seeing the competing owl, such confrontations may turn physical, with various levels of threats distinguished. The highest threat level involves the spreading of wings, bill-clapping, hissing, higher-pitched screams of longer duration, with general body poised to strike with its feet at intruder. If the intruder continues to press the confrontation, the defending owl will "hop" forward and strike it with feet, attempting to grasp and rake with claws.[15]

Territoriality appears to place a limit on the number of breeding pairs in a given area. Individuals prevented from establishing a territory live a silent existence as "floaters". Radio-telemetry revealed that such floaters concentrate along boundaries of established territories. At Kluane Lake in Yukon, incursions into neighboring territories were observed only twice—by females when a neighboring female had died or emigrated, suggesting that territorial defense may be sex-specific. At least four dead great horned owls in Kluane were apparently killed by others of their own species in territorial conflicts.[43] Owls killed by other horned owls are sometimes cannibalized, although the origin of the killing may have been territorial aggression.[73] Northern populations occasionally irrupt south during times of food shortage,[74] but there is no annual migration even at the northern limits of the great horned owl's range.[43]

Hunting behavior

His piercing yellow eyes and his ear tufts.
Closeup of great horned owl toes and talons

Hunting tends to peak between 8:30 pm and midnight and then can resume from 4:30 am to sunrise.[75] Hunting tends to be most prolonged during winter by virtue of prey being more scarce.[76] However, great horned owls can learn to target certain prey during daylight in the afternoon when it is more vulnerable, such as eastern fox squirrels (Sciurus niger) while they're building their leaf nests and chuckawallas (Sauromalus ater) sunning themselves on desert rocks.[77][78] Owls hunt mainly by watching from a snag, pole or other high perch. During hunting forays, they often fly about 50 to 100 m (160 to 330 ft) from perch to perch, stopping to survey for food at each, until they sense a prey item below. From such vantage points, owls dive down to the ground, often with wings folded, to ambush their prey.[12] Effective maximum hunting distance of an owl from an elevated perch is 90 m (300 ft).[41] Due to their short but broad wings, great horned owls are ideally suited for low speed and maneuverability.[27]

Despite reports that they do not hunt on the wing,[79] they also sometimes hunt by flying low over openings on the ground, scanning below for prey activity.[12] Great horned owls can fly at speeds of more than 65 km/h (40 mph) in level flight.[6] Hunting flights are slow, often quartering low above the ground where prey is likely to occur in open country or open woodland. Brief hovering flight (for about 6–18 seconds) has been described, especially in windy areas.[80] On occasion owls may actually walk on the ground in pursuit of small prey or, rarely, inside a chicken coop to prey on the fowl within.[22] Rodents and invertebrates may be caught on foot around the base of bushes, through grassy areas, and near culverts and other human structures in range and farm habitat.[15] The great horned owl is generally a poor walker on the ground; it walks like a starling, with a pronounced side-to-side gait. They have been known to wade into shallow water for aquatic prey, although this has been only rarely reported.[15] Owls can snatch birds and some arboreal mammals directly from tree branches in a glide as well. The stiff feathering of their wings allows owls to produce minimal sound in flight while hunting.[5][12][22]

Almost all prey are killed by crushing with the owl's feet or by incidentally stabbing of the talons, though some may be bitten about the face as well. Prey is swallowed whole when possible. When prey is swallowed whole, owls regurgitate pellets of bone and other non-digestible bits about 6 to 10 hours later, usually in the same location where the prey was consumed.[12] Great horned owl pellets are dark gray or brown in color and very large, 7.6 to 10.2 cm (3.0 to 4.0 in) long and 3.8 cm (1.5 in) thick, and have been known to contain skulls up to 3 cm (1.2 in) in width inside them.[22] However, not all prey can be swallowed at once, and owls will also fly with prey to a perch and tear off pieces with their bill. Most dietary studies focus on pellets found under perches and around nests, since they provide a more complete picture of the diversity of prey consumed, but prey remains outside of pellets may provide clues to prey excluded from the pellets and a combination of both is recommended.[6][81][82]

Many large prey items are dismembered. Great horned owls may behead large prey before taking it to its nest or eating perch. The legs may also be removed, as may (in some bird prey) the wings. The great horned owl will also crush the bones of its prey to make it more compact for carrying.[83] On occasion, the owls may return to the kill site to continue eating if the prey is too heavy to fly with after dismemberment.[7] Many owls will accrue a cache of prey, especially those who are nesting. Caches must be at a safe location, usually the crotch of a tall tree. In northern regions, where large prey is prevalent, an owl may let uneaten food freeze and then thaw it out later using its own body heat.[19] Hunting success seems to require fairly open understory, and experimental testing of microhabitat proved that open areas provided more hunting success on five species of rodent, with cloudy nights and denser bush foliage both decreasing success.[84]

Prey and trophic ecology

Painting by Louis Agassiz Fuertes depicting a great horned owl with one of its primary prey species, a snowshoe hare

Prey can vary greatly based on opportunity. According to one author, "Almost any living creature that walks, crawls, flies, or swims, except the large mammals, is the great horned owl's legitimate prey".[30] In fact, the great horned owl has the most diverse prey profile of any raptor in the Americas.[6] Over 500 species have been identified as great horned owl prey, with dozens more identified only to genus or general type (especially numerous invertebrates) and presumably several more unknown from their relatively little-studied populations in the Neotropics. Mammals (more than 200 species) and birds (nearly 300 species) make up the majority of their diet.[6][81] Their diet in North America is made up of 87.6% mammals, 6.1% birds, 1.6% reptiles and amphibians with the remaining 4.7% being made up by insects, other assorted invertebrates and fish.[6]

Estimated mass of individual prey for the owls has ranged from as little as 0.4 g (0.014 oz) to as much as 6.8 kg (15 lb)[85][86] Most prey is in the range of 4 g (0.14 oz) (shrews) to 2,300 g (5.1 lb) (jackrabbits).[85][87] A single owl requires about 50 to 100 g (1.8 to 3.5 oz) of food per day and can subsist on a large kill over several days.[88] Despite the great diversity of prey taken by these predators, in most of the continental United States from the East to the Midwest as well as Canada and Alaska, great horned owls largely live off just a handful of prey species: three species of lagomorph: the eastern cottontail (Sylvilagus floridanus), the snowshoe hare (Lepus americanus) and the black-tailed jackrabbit (Lepus californicus); two species of New World mice: the white-footed mouse and the North American deermouse (Peromyscus leucopus & maniculatus); approximately three species of vole: the meadow, prairie and woodland voles (Microtus pennsylvanicus, ochrogaster & pinetorum); and one introduced pest, the brown rat.[15][81][85]

Rodents

A large portion of the great horned owl's food consists of small rodents, such as white-footed mice.

Small rodents form the great majority of great horned owl prey by number. Weighing a mere 14 to 31.5 g (0.49 to 1.11 oz) and 20 to 58 g (0.71 to 2.05 oz) on average, the nine species of New World mice in Peromyscus and eight species voles in Microtus recorded in the diet would appear to be overly small to be as important as they are to a predatory bird of this size. The prominence of these genera is undoubtedly due to the abundance of both genera in the wooded edge habitats frequented by great horned owls. It is estimated that a family of owls with two offspring would need to take about a half dozen (voles) to a dozen (mice) of these rodents every night to satisfy their dietary requirements but apparently the accessibility and abundance of these foods is irresistible as their numeric dominance is indisputable.[23][81] By winter in areas that hold heavy snow, Peromyscus mice often come to outnumber the voles in the diet since the mice tend to travel over the surface of the snow while the voles make tunnels underneath the snow.[23][6][81] In fact, a healthy family of great horned owls can decimate a colony of field rats, thus potentially performing a key role in controlling a highly destructive pest.[81] Great horned owls living in the timbered fringes of garbage or refuse dumps may subsist mostly on rats.[19]

In the Rockies, California, the Southwestern United States and northern Mexico, the diversity of this species' diet rises, in sync with the diversity of rodents. Especially important, from Colorado to Washington state is the northern pocket gopher (Thomomys talpoides), although assorted other pocket gophers (Geomys, Cratogeomys, Zygogeomys, Pappogeomys and other Thomomys ssp.) are readily taken. While the northern weighs from 90 to 120 g (3.2 to 4.2 oz), other pocket gophers hunted average from 95 to 545 g (0.209 to 1.202 lb) in mass. From Washington to Baja California a very important food is the pocket mice, primarily the Great Basin pocket mouse (Perognathus parvus). While the Great Basin species is a relative giant at 22 g (0.78 oz), other hunted pocket mice (which may include both Perognathus and Chaetodipus ssp.) can average nearly as light as 8 g (0.28 oz). In East Texas, the 159 g (5.6 oz) hispid cotton rat (Sigmodon hispidus) is the most commonly recorded prey species.[89] The same species constituted 75% by number of a small sampling in Oklahoma.[90] In semi-desert and other arid habitats, kangaroo rats become increasingly important prey, ten species have been reported in the diet but most prominently the Ord's and Merriam's kangaroo rats (Dipodomys ordii & merriami), both being widespread, numerous and relatively diminutive (at 42 and 48 g (1.5 and 1.7 oz)). Eight known larger species of kangaroo rats, including the giant kangaroo rat (Dipodomys ingens) averaging at 152 g (5.4 oz), are also taken.[91][92][93]

The squirrels, including ground squirrels, marmots (Marmota), prairie dogs (Cynomys), chipmunks and tree squirrels, are diurnal and so are largely unavailable to great horned owls as prey. Occasionally though, one will be caught from their leaf nest, nest hole or burrow entrance first thing in the morning or in the late afternoon and approximately 35 species have been successfully predated by these owls. In general larger sized than other rodent families, the species hunting range from the 62 g (2.2 oz) gray-collared chipmunk (Tamias cinereicollis) to the 5,775 g (12.732 lb) hoary marmot (Marmota caligata); thus, squirrels can be provide a very fulfilling meal.[7][15][94] An even larger rodent is sometimes attacked as prey by great horned owls, the North American porcupine (Erethizon dorsatum), in which average adults range from 4,500 to 9,000 g (9.9 to 19.8 lb). This has been determined from owls who have porcupine quills imbedded in them, sometimes resulting in death.[7][95] On occasion, they are successful in killing porcupine, even adults as determined by the size of the quills left behind and prey remains at bloodied kill sites.[88][96][97] Other rodents recorded as secondary prey in North America include flying squirrels (Glaucomys ssp.), the golden mouse (Ochrotomys nuttalli), red-backed voles & bog lemmings (Myodes & Synaptomys ssp.), the muskrat (Ondatra zibethicus), the northern grasshopper mouse (Onychomys leucogaster), the northern pygmy mouse (Baiomys taylori) and jumping mice (Zapus & Napaeozapus ssp.).[7][15]

Lagomorphs

Black-tailed jackrabbits are an important food source for western great horned owls.

Although generally no match for rodents in sheer quantity of individuals, in terms of prey biomass, the most significant prey of North American great horned owls are hares and rabbits. About a dozen lagomorphs species are known to be hunted by the owl, from the relatively tiny 420 g (0.93 lb) pygmy rabbit to several hares weighing more than 2,000 g (4.4 lb). Two hare species, the black-tailed jackrabbit and snowshoe hare, are so important to the owls as a food source that the local owl populations sharply rise and fall in sync with the hares' cyclical population trends. With adult weights of 800 to 1,900 g (1.8 to 4.2 lb) in adult cottontails, 900 to 2,000 g (2.0 to 4.4 lb) in snowshoe hares and 1,400 to 2,700 g (3.1 to 6.0 lb) in black-tailed jackrabbits, these species are overall the largest regular prey for this species.[6]

In Utah, where great horned owls are dependent on the jackrabbits, average brood size rose from 2 at jackrabbit population lows to 3.3 when the jackrabbits were at their peak. At the peak of population cycle, jackrabbits accounted for 90.2% and desert cottontails (Sylvilagus audubonii) for another 8.7% of prey biomass.[75][98] In the short-grass prairie of Colorado, mountain cottontail (Sylvilagus nuttallii) and black-tailed jackrabbits predominated in October to December, making up 42.9% by number (and nearly all the biomass), thence dropping to 9.3% by number in April, while voles rose to 32.2% peak in May, down to a minimum of 10.2% by number in June.[6] Further north in Colorado, in the absence of jackrabbits, the mountain cottontails falls to third place by number (12.9%) behind the northern pocket gopher (36.5%) and prairie vole (24.7%) but still dominates the biomass, making up about half.[99] In central Utah, the lagomorphs (black-tailed jackrabbit/desert cottontail) and Ord's kangaroo rat each made up 39% of the food by number, respectively.[75] The mountain cottontail dominates the biomass of prey in the Sierran foothills of California, making up 61.1% of the biomass, although are numerically secondary to desert woodrat.[91] Remarkably, in the Morley Nelson Snake River Birds of Prey National Conservation Area of Idaho, individual rodents (1159 counted) were more than 10 times more numerous than lagomorphs (114 counted) by quantity and yet the jackrabbit and mountain cottontail still made up approximately half of the biomass.[100] The dependence on lagomorphs also extends into Mexico, as in Baja California about a quarter of identified prey was black-tailed jackrabbit and either desert or the larger Mexican cottontail (Sylvilagus cunicularius).[101]

In the northern boreal forest, great horned owls are even more dependent on the snowshoe hare. At the peak of the 10 year hare cycle, snowshoe hares were by far the largest component of both summer and winter diets (77–81% and 90–99%, respectively, in Alberta; 83–86% and 75–98%, respectively, in Yukon). At the lowest point of the hare's cycle, summer diets consisted of only 0–16% snowshoe hare in Alberta and 12.7% in Yukon. When hares were scarce, great horned owls in these regions fed mostly on large rodents, mice and voles, grouse and ducks. Because fewer of these alternative prey species are available in boreal forest during winter, owls had to emigrate or suffer high mortalities if they stayed.[102][103] In Alberta, the local population of great horned owls can increase threefold from hare population lows to peaks.[104] The dependency on the snowshoe hare by the great horned owl extends into Alaska as well.[105]

Other mammals

Other mammals are taken readily as well. From both the tropics and the United States, several species of opossum may be taken, down to the size of the tiny dwarf fat-tailed mouse opossum (Thylamys velutinus). In Brazil, white-eared opossum (Didelphis albiventris) were found in 12% of pellets, but all specimens appeared to be juveniles each weighing about 1,000 g (2.2 lb).[106] Quite differently, in Pennsylvania, Virginia opossum (Didelphis virginianus) made up 6% by number of prey but due to their large size (approximately 2,500 g (5.5 lb)) and that all specimens were adults, they occupied the highest percentage of biomass of any species in a wide study from that state.[107] At least eight species of shrews are taken by opportunity and make up the smallest mammalian prey taken by great horned owls, as specimens of least shrew (Cryptotis parva) or masked shrew (Sorex cinereus) have had an estimated weight of only 2 g (0.071 oz).[85]

One of the more regularly taken shrews, though, is the larger 19.5 g (0.69 oz) northern short-tailed shrew (Blarina brevicauda), which was represented in more than 2% of pellets in the Upper Midwest.[81] Moles, of at least four or five species, are also widely but lightly reported as prey.[81][85] Remnants of armadillo, presumably nine-banded armadillo (Dasypus novemcinctus), have been found around owl nests in the south.[7] 11 species of bat are known to be hunted by great horned owls.[6][108][109][110] One pellet in Texas was found to be composed entirely of Mexican free-tailed bats (Tadarida brasiliensis).[111] Smaller species of mammalian carnivore, such as ringtail (Bassariscus astutus), American mink (Neogale vison), black-footed ferret (Mustela nigripes) and various other small mustelids (Mustela ssp.), are sometimes taken as prey.[7][15][112][113] Prey in the form of canids, like foxes or coyotes (Canis latrans) are often juveniles presumably snatched from the mouths of dens by night.[7][15][114][115][116] Kit and swift foxes of up to adult size may taken.[88][117][118]

Surprisingly, at least two cases of a great horned owl preying on an adult raccoon (Procyon lotor) have been reported.[119][120] One instance of an owl taking a bobcat (Lynx rufus) as prey was also reportedly observed.[88] In one case, a great horned owl was the likely killer of an adult female fisher (Martes pennanti), though young ones are typically taken.[121][122] Occasionally, domestic carnivores are also prey. A few cases of young or small dogs (Canis lupus familiaris)[123][124] and several of juvenile and adult cats (Felis silvestris catus)[125][126][127] being killed by great horned owls have been reported.[7][116][128] The most infamous predatory association amongst relatively larger carnivores is that with skunks. Due to their poor sense of smell, great horned owls are the only predators to routinely attack these bold mammals with impunity. All six skunk species found in North America are reported as prey, including adult striped skunks (Mephitis mephitis), which can be three times as heavy as the attacking owl.[7][85][129] In one single nest, the remains of 57 striped skunks were found.[130] Due to the proclivity of skunk predation, great horned owls nests frequently smell strongly of skunk and occasionally stink so powerfully of skunk that they leave the smell at kill sites or on prey remains.[15][131]

Birds

American coots are often a favored food source for great horned owls living near wetlands.

After mammals, birds rank as the next most important general prey group. Birds are usually considerably secondary in the diet but outnumber the mammals in the diet by diversity, as more than 250 species have been killed in North America alone. Statistically, the most significant avian prey seems to be galliforms, of which they are known to have preyed on 23 species, basically consisting of all of the native species found in the United States.[7][15] In the Upper Midwest, the ring-necked pheasant (Phasianus colchicus) and northern bobwhite (Colinus virginianus) were the fifth and sixth (out of 124 identified species) most significant prey species in 4838 pellets.[81] Errington characterized the predatory pressure exerted on bobwhites by great horned owls as "light but continuous pressure", which may be considered characteristic of the species' hunting of all galliforms.[132]

Usually coveys of quail are partially protected by spending the night roosting communally in dense thickets but should a hunting owl be able to track down the communal roost, losses can be fairly heavy until the roost relocates.[23] Similarly, owls may track down sleeping grouse, which also roost in vegetation but more openly than quail. Some grouse, such as greater prairie chicken (Tympanuchus cupido), sharp-tailed grouse (Tympanuchus phasianellus) and greater sage-grouse (Centrocercus urophasianus), may also been vulnerable to great horned owls while displaying conspicuously in openings on a lek first thing in the morning.[133] In the boreal forest, especially in years where the snowshoe hare experiences population decreases, great horned owls prey fairly heavily (approximately 25% of biomass) on ruffed grouse (Bonasa umbellus) and spruce grouse (Falcipennis canadensis), enough so in the earlier bird to possibly contribute to population reductions.[102][134] Larger species of galliform are not immune to predation either. On Protection Island in Washington state, introduced common peafowl (Pavo cristatus) are an important prey item.[135] The wild turkey (Meleagris gallopavo), 4 to 8 kg (8.8 to 17.6 lb) on average between the sexes, is probably the largest bird the great horned owl hunts in which they kill adults. Both full-grown wild turkeys[136] and adult domestic turkeys[7] have been hunted and killed. Under normal circumstances, domestic chicken (Gallus gallus domesticus) will be ignored in favor of wild prey. On occasion, individual owls, especially inexperienced juveniles, will become habitual fowl killers. These errant owls mainly hunt chickens, though will also take domestic guineafowl, turkeys and anything else available.[81] In general, chickens kept in locked cages with enclosed tops overnight are safe from great horned owls; not so chickens left free range or in open enclosures.[7]

While galliforms are widely reported, the few cases where great horned owls locally turn to birds as the primary food source over mammals, these may often be local responses to the abundance of breeding water birds or concentrations of roosting water birds, since they tend to roost in relatively open spots. They have been known to predate more than 110 different species of assorted water bird.[6] In prairie wetlands of North Dakota, avian prey, primarily represented by ducks and the American coot (Fulica americana) came to represent 65% by number and 83% by biomass of the diet of the local owls, also including secondarily grebes, smaller rails, loons, shorebirds and seabirds, as well as upland-based species like grey partridge (Perdix perdix), sharp-tailed grouse and passerines.[137] 77% of the ducks in that study were juveniles, the largest duck being a male mallard (Anas platyrhnychos) weighing approximately 1,250 g (2.76 lb), but nearly all the coots were adults.[86] On Protection Island, Washington, where they are no native land mammals, rhinoceros auklets (Cerorhinca monocerata), both adults and nestlings, were the most numerous prey, present in 93% of 120 pellets.[135] Species as large as adult Canada geese, snow goose[7][81] and great blue herons[15] have been successfully killed. Medium-sized birds of prey (even other species of owl) are also taken.[138] The nestlings of even larger species like trumpeter swans (Cygnus buccinator),[139] American white pelicans (Pelecanus eryhtrorhynchos),[140] brown pelicans (Pelecanus occidentalis)[141] and sandhill cranes (Grus canadensis)[142] have also been killed by these owls.

Other assorted birds are taken seemingly at random opportunity. The predatory effect of this species on other raptorial birds, which is often considerable, is explored in the following section. In Brazil, it was found in a small study that birds overall outnumbered mammals in pellets, although most were not determined to species and the ones that were shown a tremendously diverse assemblage of birds with no obvious dietary preference.[106] Although not usually numerically significant, 86 species of passerine have been taken by great horned owls. Members from most North American families are known as prey, although among smaller types such as chickadees, warblers, sparrows, cardinals, wrens and most tyrant flycatchers only a few species from each have been recorded. Nonetheless, an occasionally unlucky migrant or local breeder is sometimes snatched.[6][7][81] Fledgling songbirds are regularly taken in spring and summer.[88] The smallest avian prey known for great horned owls are the 5.8 g (0.20 oz) blue-grey gnatcatcher (Polioptila caerulea) and the 6.2 g (0.22 oz) ruby-crowned kinglet (Regulus calendula).[81] Somewhat larger bodied families are more prominent, i.e. the corvids (14 species) and icterids (14 species) and, secondarily, the kingbirds (Tyrannus ssp.), thrushes, mimids and European starling (Sturnus vulgaris).[6][7][81] This is likely due to the fact that the larger passerines usually roost in relatively open spots and have larger, more conspicuous nests. Crows and ravens tend to be grabbed off of their communal roosts by night.[15]

Other prey

The great horned owl rarely misses an opportunity to hunt reptiles and amphibians. However, lizards are largely unavailable as prey due to their typically diurnal periods of activity.[15] However, some snakes are partially or largely nocturnal, and more than a dozen species are hunted in North America. Snakes hunted range from small, innocuous garter snakes (Thamnophis ssp.) and night snakes (Hypsiglena torquata) to venomous species like cottonmouths (Agkistrodon piscivorus) and prairie rattlesnakes (Crotalus virdis) and formidable, large species like common king snakes (Lampropeltis getula) and black rat snakes (Pantherophis obsoletus), which in mature specimens can rival the owl in mass and sheer predatory power.[7] The capture of the hatchlings of very large reptiles such as loggerhead turtles (Caretta caretta) and American alligators (Alligator mississippiensis) by great horned owls has been reported, in both cases likely when the baby reptiles are attempting to make their way to the security of water.[7][143] On rare occasion, salamanders, frogs and toads are reported as prey. On rare occasions, fish are taken including goldfish (Carassius auratus), bluegill (Lepomis macrochirus), bullheads (Ameiurus ssp.), other catfish, suckers, sunfish, eels and dace and chub.[7][88]

Many types of invertebrates are recorded as prey. These include mainly insects, but also crayfish, crabs, centipedes, spiders, scorpions and worms.[137] The occasionally invertebrate prey taken largely consists of common, large insects such as various beetles, crickets, grasshoppers, water bugs and katydids, some of which the great horned owl has even reportedly caught via "hawking", i.e. swooping at on the wing.[7][15][144] In some cases, the content of insects in great horned owl pellets may actually be due to the owls eating other birds which have freshly eaten insects in their own stomachs.[81] It is commonly believed that routine insectivory in great horned owls is mainly restricted to inexperienced young owls too unskilled to graduate to larger prey yet. It is clearly inefficient for owls of this size to attempt to raise young on a diet of foods as small as insects.[29] Although rare, carrion-feeding has been recorded in great horned owls, especially ones wintering in Canada and other northern areas during harsh weather.[145] Road kills are sometimes opportunistically eaten. A case of an owl scavenging a white-tailed deer (Odocoileus virginianus) carcass, ultimately tearing off the deer's leg, was captured on a motion capture video camera set out to film wildlife.[146]

Urban vs rural diet

Studies comparing the diets of rural and urban great horned owls have identified that the most abundant rodent prey in their environment fulfils the majority of their diet.[147][148][149][150] A study of food niche overlap between closely nested barn and great horned owls living in rural north-eastern Oregon identified voles as by far the most common prey.[148] In southwestern British Columbia, Townsend's voles were the most common prey species, while consumption of rats increased as the nesting location became more urban and rats replaced voles as the most abundant and stable food source.[147] A similar focus on rats was found in populations in urban parks in Seattle.[151] Although a stable and highly abundant food source, a diet consisting of primarily rats can be harmful to urban great horned owls due to bioaccumulation of rodenticides.[152]

Interspecific predatory relationships

An immature red-tailed hawk eats a vole, one of the many prey items that feed both the competing hawks and great horned owls.

Due to their very broad dietary habits, the great horned owls share their prey with many other predators, including avian, mammalian and reptilian ones. Almost every study comparing the diets of North American owls illustrates the considerable overlap in the dietary selection of these species, as all species, besides the primarily insectivorous varieties, rely on many of the same small rodent species for most of their diet, extending from the small northern saw-whet owl and eastern screech owl to the great horned and great grey owls.[29][85]

In a long-term study of a block of Michigan, all nine species of accipitrid, falcon and owl that stayed to breed there were found to be primarily dependent on the same two rodent genera, the meadow vole and the two common Peromyscus species.[23] In the Great Basin, the owls share black-tailed jackrabbit and desert cottontail as the primary prey with golden eagles, red-tailed hawks and ferruginous hawks (Buteo regalis); all four species had diets with more than 90% of the biomass is made up of those lagomorphs. Of these, the great horned owl and golden eagle were able to nest most closely to one another because they had the most strongly dissimilar periods of activity.[62][98] In California, when compared to the local red-tailed hawks and western diamondback rattlesnakes (Crotalus atrox), the diets were most similar in that by number about 15-20% of all three species' diets depended on cottontails, but the largest portion was made up of ground squirrels in the hawk and the rattlesnake and desert woodrats and other assorted rodents in the great horned owl.[91] In the boreal forests, the great horned owl's prolificacy as a snowshoe hare hunter places it second only to the Canada lynx (Lynx canadensis) among all predators. Although locally dependent on the hares as their main food, northern goshawks (Accipiter gentilis), red-tailed hawks and golden eagles apparently do not have as large of an impact on the hares, nor do mammalian carnivore generalists that also kill many hares, like the fisher, bobcat, wolverine (Gulo gulo), coyote and larger varieties (i.e. wolves (Canis lupus), cougars (Puma concolor) and bears (Ursus ssp.)).[43][74][104][153]

The relationship between great horned owls and other raptorial birds in its range is usually decidedly one-sided. While certain species, such as the red-tailed hawk and northern goshawk, might be seen as potential competition for the owls, most others seem to be regarded merely as prey by great horned owls. The great horned owl is both the most prolific and diverse predator in America of other birds of prey, with other accomplished raptor-hunters such as the goshawk and the golden eagle being more restricted in range, habitat and number in North America and thus having a more minor impact. All studies have found raptors are a small portion of this owl's diet but predation can be seriously detrimental for such prey, as raptors tend to be territorial and sparsely distributed as a rule and thus can be effectively decimated by a small number of losses.[6][85] In the gray hawk (Buteo plagiatus), for example, in a study of one breeding block of Arizona, the owls were observed to visit nests nightly until all the nestlings were gone.[154]

Raptorial birds in general tend to have large, conspicuous nests which may make them easier for a hunting owl to locate. The great horned owl gains an advantage by nesting earlier than any other raptor in its range (indeed any bird), as it is able to exploit the other raptors as food while in a more vulnerable state as their own nestlings have become well developed.[23] On average, great horned owls begin nesting about three weeks before red-tailed hawks begin to build nests, although some raptors may locally breed as much as two months after the owls.[15][155]

More so than diurnal varieties of raptor, fairly significant numbers of owls are hunted, as all species are to some extent nocturnal and thus their corresponding activity can attract the horned owl's unwanted attention. The extent of predation on other owls depends on the habitat preferences of the other species. Eastern and western screech owls may be most vulnerable since they prefer similar wooded edge habitat. In a block of Wisconsin, great horned owls were responsible for the failure of 78% of eastern screech owl's nests.[23] Long-eared owls and, to a lesser extent, barn owls tend to hunt in open, sparsely treed habitats more so than great horned owls, but since they may return to wooded spots for nesting purposes, they may be more vulnerable there. The long-eared owl and barn owls are often compared to the great horned owl as these medium-sized species often occur in abutting habitats and often hunt primarily the same vole and mice species, although the alternate prey of the great horned tends to be much larger, including the smaller owls themselves.[26][79][156] In a pair of studies from Colorado, the average weight of prey for long-eared owls was 28 to 30 g (0.99 to 1.06 oz), 46 to 57.1 g (1.62 to 2.01 oz) for barn owl and 177 to 220 g (6.2 to 7.8 oz) for the great horned owl.[29][99]

Both young and adult great grey owls, despite their superficially superior size, are apparently hunted with impunity by great horned owls. In the boreal forests, both the northern hawk owl and great grey owl appear to be in greater danger of great horned owl predation in years where the snowshoe hare have low populations.[157][158] Great horned owls were the leading cause of mortality in juvenile spotted owls (30% of losses) and juvenile great grey owls (65% of losses).[157][159] Less is known about relations with the snowy owl, which may compete with great horned owls for food while invading south for the winter. Anecdotally, both snowy and great horned owls have rarely been reported to dominate or even kill one another depending on the size and disposition of the individual owls, although the snowy's preference for more open areas again acts as something of a buffer. The snowy may be the one North American owl too formidable for the great horned owl to consider as prey.[13]

Whereas owls of any age are freely attacked by great horned owls whether nesting or not, when it comes to diurnal raptors, great horned owls are mainly a danger around the nest. They often hunt diurnal raptors when they come across their often relatively conspicuous active platform nests during hunting forays in spring and summer, taking numbers of both nestlings and brooding adults.[15] Again, like owls, diurnal raptors are attacked depending on the relative similarity of their habitat preferences to the owl. Cooper's hawks (Accipiter cooperii) and red-tailed hawks tend to be most vulnerable, as they prefer the same wooded edges frequented by great horned owls. Other diurnal raptors may be attracted to more enclosed wooded areas, such as sharp-shinned hawks (Accipiter striatus) or zone-tailed hawks (Buteo albonotatus), or more open plain and meadow areas, such as Northern harriers (Circus hudsonius) and ferruginous hawks, but this is almost never a total insurance against predation as all of these are recorded prey.[81][160][161][162]

In a study of red-shouldered hawk (Buteo lineatus) and broad-winged hawk (Buteo brachyurus) breeding in New York, despite their nesting in deeper woods than those that host these owls, the main cause of nest failure was great horned owl predation.[131] Similarly, the great horned owl was the primary cause of nesting failure for both desert-dwelling Harris's hawks (Parabuteo unicinctus) and forest-dwelling northern goshawk in Arizona (39% and 40% of failures, respectively), wetland-inhabiting osprey (Pandion haliaetus) in Delaware (21% of failures) and peregrine falcons (Falco peregrinus) in the Western United States (27% of failures).[163][164][165][166] The fact that many of the nests great horned owls use are constructed by accipitrids may lead to localized conflicts, almost always to the detriment of the hawks rather than the owls. While the young of larger diurnal raptors are typically stolen in the night, great horned owls also readily kill large adult raptors both in and out of breeding seasons, including osprey, northern goshawk and rough-legged buzzard.[167][168][169]

Great horned owls are frequently mobbed by other birds. Most accipitrids will readily mob them, as will falcons. Hen harriers, northern goshawks, Cooper's hawks, Harris's hawks, red-tailed hawks, Swainson's hawks, ferruginous hawks, red-shouldered hawks, American kestrels, peregrine falcons, prairie falcons (Falco mexicanus) and common ravens (Corvus corax) are among the reported species who have been recorded diving on great horned owls when they discover them.[15][82][170][171] In Arizona and Texas, they may be mobbed by Mexican jays and western scrub jays (Aphelocoma wollweberi & californica) and western and Cassin's kingbirds (Tyrannus verticalis & vociferans).[172][173] In addition, there are several documented incidences of American crows mobbing a great horned owl, in groups of dozens or even hundreds of crows.[7] In response to mobbing, if the owl flies it alights to the nearest secluded spot. If an owl alights on ground or on exposed branch or ledge, it may respond to swooping and stooping flights of corvids and raptors with threat display and raising of its wings.[15]

Reproduction

Nestlings of the Rocky Mountains great horned owl (B. v. pinorum) in New Mexico
Juvenile coastal great horned owls (B. v. saturatus) near Tule Lake National Wildlife Refuge, Oregon, United States

Great horned owls are some of the earliest-breeding birds in North America, seemingly in part because of the lengthy nightfall at this time of year and additionally the competitive advantage it gives the owl over other raptors. In most of North America, courtship is from October to December and mates are chosen by December to January.[12] This species was once thought to be strictly monogamous, but recent analysis indicates one male may mate with two females simultaneously, as was discovered for the first time in 2018 in Reno, Nevada.[174] During courtship in late fall or early winter, the male attracts the attention of his mate by hooting emphatically while leaning over (with the tail folded or cocked) and puffing up his white throat to look like a ball.[12] The white throat may serve as a visual stimulus in the low light conditions typical of when this owl courts.[43] He often flies up and down on a perch, while approaching the potential mate. Eventually, he comes to approach the female and tries to rub his bill against hers while repeatedly bowing. If receptive, the female hoots back when the pair meet but is more subdued in both her hoot and display. The male may convince the female by bringing her freshly caught prey, which they will share.[7][12] While males often hoot emphatically for about a month or six weeks towards the end of the year, the period where females also hoot is usually only a week to ten days.[42] Pairs typically breed together year after year and may mate for life, although they associate with each other more loosely when their young become mostly independent.[12] Pairs rekindling their reproductive relationship in the winter may perform a milder courtship to strengthen pair bonds before producing young.[42]

Males select nesting sites and bring the females' attention to them by flying to the nest and then stomping on it.[12] Considering the owls' large size, nests with open access are preferred to those enclosed with surrounding branches. Like all owls, great horned owls do not build their own nest. Great horned owls tend to examine an area for an abandoned nest, generally from larger birds like hawks, and take over the nest for raising their own young.[175] They nest in a wider variety of sites than any other North American bird.[42] Many nests are in cavernous hollows of dead trees or their branches, and especially in southern states in large trees along the edge of old-growth lots.[42] In mountainous or hilly areas, especially in canyons of the Southwest and Rocky Mountains, cliff ledges, small caves, and other sheltered depressions may be used.[42] Owls living in prairie country, in the absence of other animals' nests, riparian tree-hollows or man-made structures, will use boulders, buttes, railroad cuts, low bushes and even the bare ground as nest sites.[42] Ground nests have also been recorded in the midst of tall grasses in Florida and in the midst of brushy spots on desert ground.[6] Even the burrow entrances of American badger and coyote dens have reportedly been used as nests, in spite of the inherent risk of sharing space with such potentially dangerous co-inhabitants.[42] Nesting behavior for the great horned owl appears to be more closely related to prey availability than it does to seasonal conditions. There has been some evidence that if prey availability is low enough then the species may forgo mating entirely for a season. Male and female owls of the species have been observed to help incubate the eggs once they have been laid on a nest.[176]

A brooding female common great horned owl (B. v. virginianus) on her nest in Louisiana

Most tree nests used by great horned owls are constructed by other animals, often from a height of about 4.5 to 22 m (15 to 72 ft) off the ground. They often take over a nest used by some other large bird, sometimes adding feathers to line the nest but usually not much more. Allegedly there have some cases where the owls have reinforced a nest structure or appeared to have reconstructed a nest, but as a rule no owl species has ever been known to actually build a nest.[42] Great horned owls in the Southwest may also use nests in cacti, built by Harris's hawk and red-tailed hawk, as well as large hollows in cacti.[177] The nests they use are often made by most larger types of acciptrids, from species as small as Cooper's hawks to bald eagle and golden eagle, though perhaps most often those of red-tailed hawks and other buteonines. Secondly in popularity are crow and raven (Corvus ssp.) nests. Even Canada goose, black-crowned night heron (Nycticorax nycticorax) and great blue heron nests have been used, the latter sometimes right in the midst of an active heronry.[178][179] The leaf nests of squirrels are also regularly used but in general great horned owls are partial to stick nests since they provide a much firmer, safer foundation.[15]

The stage at which eggs are laid is variable across North America. In Southern Florida, eggs may be laid as early as late November to as late as early January. In the southeast, from south Texas to Georgia, egg laying may begin from late December to early February. From Southern California to northern Louisiana, egg laying is from early February to late March. The largest swath of egg-laying owls from central California to South Carolina to as far north as Ohio and Massachusetts is from late February to early April. In the Rocky Mountains, Northwestern United States, northern New England and eastern Canada, egg laying is from early March to late April. In the rest of Canada and Alaska, egg laying may be from late March to early May.[42] The latest known date of egg laying was in mid-June in Saskatchewan and the Yukon Territory.[180] In northwestern Utah and north-central Alberta, egg-laying can be 3–4 weeks earlier than usual when food is abundant and weather is favorable.[15] For owls found in more tropical climates, the dates of the breeding season are somewhat undefined.[12] There are usually 2 eggs per clutch, but clutches range in size from 1 to 6 eggs (over 3 is uncommon, over 4 is very rare), depending on environmental conditions.[181][182] The average egg width is 46.5 mm (1.83 in), the average length is 55 mm (2.2 in) and the average weight is 51 g (1.8 oz), although mass could be slightly higher elsewhere because this figure is from Los Angeles County, CA where the owls are relatively small.[183] The incubation period ranges from 28 to 37 days, averaging 33 days.[184] The female alone usually does all the incubation and rarely moves from the nest, while the male owl captures food and brings it to her, with the first nightly food delivery typically occurring soon after dark.[15]

The young weigh 34.7 g (1.22 oz) at birth on average and can gain about 33 g (1.2 oz) a day for the first four weeks of life, with typical weights in the range of 800 or 1,000 g (1.8 or 2.2 lb) by 25–29 days for males and females, respectively.[183][184] When first hatched the young are covered in whitish gray down, with some brownish about the wings. Gradually the soft juvenal downy plumage comes through the down, being typically a cinnamon-buff color, but with variable hues predicting the eventual color of the mature owls. The extent of down gradually diminishes, developing mature-looking plumage by late summer, although many first year birds still have scattered bits of down into autumn. By late autumn, first-year birds look similar to adults but with a slightly warmer, reddish tinge, less well developed ear tufts and a smaller white throat patch.[7] The nestling owls develop mostly in behavior between two weeks and two months of age, in which time they adapt the ability to defend themselves, grasp foods and climb. Vocally, the young are able to exert weak chips while still in the egg, developing into a raspy chirp shortly after hatching. The calls of the young increase rapidly in intensity, pitch and character, some juvenile males mimicking their father's hooting in fall but usually they conclude with various odd gurgling notes. The earliest competent hooting by juvenile owls is not until January.[15][185] Young owls move onto nearby branches at 6 weeks and start to fly about a week later. However, the young are not usually competent fliers until they are about 10 to 12 weeks old.[12] The age at which the young leave the nest is variable based on the abundance of food.[104]

The young birds stay in an area ranging from 13 to 52 ha from the nest into fall, but will usually disperse up to several thousand hectares by the end of fall.[186][187] The offspring have been seen still begging for food in late October (5 months after leaving the nest) and most do not fully leave their parents territory until right before the parents start to reproduce for the next clutch (usually December to January).[188] Birds may not breed for another year or two, and are often vagrants ("floaters") until they establish their own territories.[43] Based on the development of the bursa, great horned owls reach sexual maturity at two years of age.[189]

Adult common great horned owl (B. v. virginianus) with juvenile in nest near Madison, Wisconsin

Urban vs rural nesting

While urban and rural populations show little difference in productivity, there are differences in nest selection.[190][191] Rural owls use old raptor nests more frequently than urban birds, who utilize crow or squirrel nests. Additionally, urban nesting individuals utilize trees that are taller/wider in diameter and nest much higher compared to rural nesting Great Horned Owls. The reason behind this increased tree height is due to the fact that urban areas have large trees used for ornamentation, shade and shelter. The higher nesting within the taller trees was attributed to human avoidance. Both rural and urban nesting sites were often within range of paved roads, likely a result of the great horned owl’s tendency to hunt along roadways[190]

Studies have shown that nesting in urban areas can influence adult great horned owls to lay eggs earlier than those who nest in rural areas. In Wisconsin, eggs in urban nests hatched a month earlier (January rather than February) than their counterparts in rural areas, probably due to increased protection from wind and cold.[192] Nesting owls at sites in Winnipeg, Manitoba began nesting five to six weeks earlier than those in rural parts of Manitoba, presumably due to experiencing an extremely warm winter by Winnipeg’s standards, as well as benefitting from the local urban heat island.[193]

Mortality and longevity

Longevity and natural mortality

Great horned owls seem to be the most long-living owl in North America. Among all owls, they may outrank even the larger Eurasian eagle owl in known longevity records from the wild,[6] with almost 29 years being the highest age for an owl recorded in North America.[194] In captivity, the record for the longest lived great horned owl was 50 years.[195] A more typical top lifespan of a great horned owl is approximately 13 years.[19] In general, great horned owls are most vulnerable in the early stages of life, although few species press attacks on the owl's nests due to the ferocious defensive abilities of the parents. Occasionally, nestlings and fledglings will fall from the nest too early to escape or to competently defend themselves and fall prey to foxes, bobcat, coyotes, or wild or feral cats. Occasionally raccoons and American black bears consume eggs and nestlings from tree nests and Virginia opossum may take the rare unguarded egg.[6][15] Crows and ravens have been reported eating eggs and small nestlings. This can normally only happen when owls are driven from the nest by human activity or are forced to leave the nest to forage by low food resources but on occasion huge flocks of crows have been able to displace owls by harassing them endlessly.[7][15] In general, great horned owls rarely engage in siblicide, unlike many other raptorial birds. Siblicide occurred at 9 of 2,711 nests in Saskatchewan.[74] Most cases where young owls are killed and/or consumed by their siblings or parents appear to occur when the nestling is diseased, impaired or starving or is inadvertently crushed.[81] Adults generally have no natural predators, excepting both North American eagles and other owls of their own species.[7]

Occasionally, great horned owls may be killed by their own prey. Although typically able to kill skunks without ill effect, five owls were found blind after getting sprayed in their eyes by skunks.[196] Cases where the quills of porcupines have killed or functionally disabled them have been observed as well.[95] Violent fights have been observed between great horned owls after attempts to capture rat snakes and black racers.[7][197][198] When a peregrine falcon repeatedly attacked a great horned owl near its nest along the Hudson River, it was apparently unable to dispatch the larger raptor despite several powerful strikes.[199] During their initial dispersal in fall, juvenile owls have a high mortality rate, frequently more than 50%.[15] For owls in the Yukon Territory, juvenile survival in the 9 weeks after dispersal has dropped from 80% to 23.2% in a span of three years in response of instability of food supply. In the Yukon, adults on territory had an average annual survival rate of 90.5%.[43] Anemia, caused by Leucocytozoon ziemanni and the drinking of blood by swarming, blood-drinking blackflies (Simulium ssp.), was a leading cause of juvenile mortality in the Yukon.[66]

Human-related mortality

The great horned owl is not considered a globally threatened species by the IUCN.[1] Including the Magellanic species, there are approximately 5.3 million wild horned owls in the Americas.[19] Most mortality in modern times is human-related, caused by owls flying into man-made objects, including buildings, cars, power lines, or barbed wire.[15] In one study, the leading cause of death for owls was collision with cars, entanglement with wires, flying into buildings and, lastly, electrocution.[200] Among 209 banded nestlings in yet another study, 67% were found dead after independence: 56 were found shot, 41 were trapped, 15 hit by cars, 14 found dead on highways and 14 electrocuted by overhead power lines.[201] Secondary poisoning from pest control efforts is widely reported variously due to anticoagulant rodenticides, strychnine, organophosphates (famphur applied topically to cattle (Bos primigenius taurus)), organochlorines, and PCBs.[202][203][204][205][206][207]

Frequently, the species were denominated a pest due to the perceived threat it posed to domestic fowl and potentially small game. The first genuine nature conservationists, while campaigning against the "Extermination Being Waged Against the Hawks and Owls", continued to advocate the destruction of great horned owls due to their predatory effect on other wildlife.[6] Thus, small bounties were offered in trade for owl bodies. Around the turn of the 20th century, the great horned owl was considered endangered in the state of Michigan because of the large number of poachers who were illegally hunting and collecting it.[208] Hunting and trapping of great horned owls may continue on a small scale but is now illegal in most countries.

Effect on conservation-dependent species

Occasionally, these owls may prey on threatened species. Following the devastation to its populations from DDT, the reintroduction of the peregrine falcon to the Mississippi and Hudson Rivers was hampered by great horned owls killing both young and adult peregrines at night.[209] Similarly, as mainly recorded in New England, attempts to reintroduce ospreys, after they were also hit hard by DDT, were affected by heavy owl predation on nestlings, and the owls were also recorded to take a large toll locally on the threatened colonies of roseate terns.[15] Where clear-cutting occurs in old-growth areas of the Pacific Northwest, spotted owls have been badly affected by considerable great horned owl predation.[40][210] While at least the ospreys and peregrines have rebounded admirably nonetheless, bird and mammal species that are much rarer overall sometimes fall prey to great horned owls, many in which even sporadic losses can be devastating. Among the species considered threatened, endangered or critically endangered by the IUCN which are also known to be killed by great horned owls are Townsend's ground squirrels (Urocitellus townsendii),[100] Pacific pocket mice (Perognathus pacificus),[211] giant kangaroo rats,[212] Stephens' kangaroo rat (Dipodomys stephensi),[213] black-footed ferrets,[214] greater and lesser prairie chickens,[215][216] marbled murrelets (Brachyramphus marmoratus),[217] ivory-billed woodpeckers, Florida scrub jays (Aphelocoma coerulescens),[218] pinyon jays,[219] Kirtland's warblers (Setophaga kirtlandii)[220] and rusty blackbirds (Euphagus carolinus).[132] The American Bird Conservancy's "green list" includes birds with considerable population declines (many classed as near threatened by the IUCN) or other immediate threats and/or restricted populations. Altogether, great horned owls hunt 50 different species from that list.[6][221]

Iconography and myth

Many warrior-based tribes of Native Americans admired the great horned owl for their "strength, courage and beauty".[88] The Pima of the Southwest believed that owls were reincarnations of slain warriors who fly about by night. The Arikara of the Great Plains had mystic owl societies in which initiates were made to adorn a facial mask made of the wing and tail feathers of great horned owls. Some Indian nations regarded the great horned owl as a friendly spirit that could aid in matters of love, such as the Passamaquoddy of Maine, who felt the call of this species was a magical love flute designed to ignite human passions. The Hopi of the Southwest also associated this owl with fertility, albeit of a different kind: they believed the calling of the owls into summer predicted hot weather, which produced good peach crops. During the winter solstice, the Hopi performed a ceremony with great horned owl feathers in hopes of summoning the heat of summer. Tribes in New Mexico were known to use owl wing-feathers to produce arrows which could strike their enemies with a minimum of sound. The Zuni held owl feathers in their mouths hoping to gain some of the silence that owls use in ambushes while striking their own enemies from other tribes. The Iroquois felt the origin of the great horned owl was due to an unformed owl annoying Raweno, the almighty creator, while Raweno created the rabbit, causing Raweno to make the owl "covered with mud" (dark camouflage) and doomed to ceaselessly call "whoo whoo", which he used while harassing Raweno by night because Raweno was active during the day.[88]

Provincial bird

The great horned owl is the provincial bird of Alberta.[222]

References

  1. ^ a b BirdLife International (2018). "Bubo virginianus". IUCN Red List of Threatened Species. 2018: e.T61752071A132039486. doi:10.2305/IUCN.UK.2018-2.RLTS.T61752071A132039486.en. Retrieved 20 February 2022.
  2. ^ "Appendices | CITES". cites.org. Retrieved 2022-01-14.
  3. ^ Seton, Ernest E. T. (January 1885). "Manitoban Notes" (PDF). The Auk. 2 (1): 21–24. doi:10.2307/4625166. JSTOR 4625166 – via JSTOR.
  4. ^ a b Austing, G.R.; Holt, Jr., J.B. (1966). The World of the Great Horned Owl. Philadelphia: Lippingcott Company. ASIN B0006BN8QG.
  5. ^ a b "Great Horned Owl". The Cornell Lab of Ornithology. Archived from the original on 5 July 2017. Retrieved 21 March 2013.
  6. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al Voous, K.H. (1988). Owls of the Northern Hemisphere. MIT Press. ISBN 0262220350.
  7. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae Bent, Arthur Cleveland (1938). Life Histories of North American Birds of Prey. Bulletin of the United States National Museum, No. 170. Vol. 2: Orders Falconiformes and Strigiformes. Washington, DC: Smithsonian Institution. pp. 295–348. hdl:10088/10016.
  8. ^ Gmelin, Johann Friedrich (1788). Systema naturae per regna tria naturae : secundum classes, ordines, genera, species, cum characteribus, differentiis, synonymis, locis (in Latin). Vol. 1, Part 1 (13th ed.). Lipsiae [Leipzig]: Georg. Emanuel. Beer. p. 287.
  9. ^ Edwards, George (1747). A Natural History of Uncommon Birds. Vol. Part 2. London: Printed for the author at the College of Physicians. p. 60; Plate 60.
  10. ^ Duméril, A. M. Constant (1805). Zoologie analytique : ou, Méthode naturelle de classification des animaux; endue plus facile a l'aide de tableaux synoptiques (in French). Paris: Allais. p. 34. The book bears the date of 1806 on the title page but was actually published in 1805. See: Gregory, Steven M.S. (2010). "The two 'editions' of Duméril's Zoologie analytique, and the potential confusion caused by Froriep's translation Analytische Zoologie" (PDF). Zoological Bibliography. 1 (1): 6–8.
  11. ^ a b Gill, Frank; Donsker, David; Rasmussen, Pamela, eds. (August 2022). "Owls". IOC World Bird List Version 12.2. International Ornithologists' Union. Retrieved 24 December 2022.
  12. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am König, Claus; Weick, Friedhelm (2008). Owls of the World (2nd ed.). London: Christopher Helm. ISBN 9781408108840.
  13. ^ a b Potapov, E.; Sale, R. (2013). The Snowy Owl. Poyser Monographs. A&C Black. ISBN 978-0713688177.
  14. ^ Risdon, D.H.S. (1951). "The rearing of a hybrid Virginian x European Eagle-Owl at Dudley Zoo". Avicultural Magazine. 57: 199–201.
  15. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at Artuso, C.; Houston, C. S.; Smith, D. G.; Rohner, C. (2020). Poole, A. F. (ed.). "Great Horned Owl (Bubo virginianus), version 1.0". Birds of the World. Ithaca, NY, USA: Cornell Lab of Ornithology. doi:10.2173/bow.grhowl.01.
  16. ^ Brodkorb, P. (1971). "Catalogue of fossil birds, Part 4 (Columbiformes through Piciformes)". Bulletin of the Florida State Museum, Biological Science. 15 (4).
  17. ^ Miller, L. H. (1911). "Avifauna of the Pleistocene cave deposits of California". University of California Bulletin, Department of Geology. 6: 385–400.
  18. ^ Olson, S. L. (1984). "A very large enigmatic owl from the late Pleistocene at Ladds, Georgia". Special Publication, Carnegie Museum of Natural History. 8: 44–46.
  19. ^ a b c d e f g h i Mikkola, H. (2012). Owls of the World: A Photographic Guide. Firefly Books. ISBN 9781770851368.
  20. ^ a b c d e Mcgillivray, W. B. (1989). "Geographic variation in size and reverse size dimorphism of the Great Horned Owl in North America". Condor. 91 (4): 777–786. doi:10.2307/1368060. JSTOR 1368060.
  21. ^ a b c d Webster, J. D.; Orr, R. T. (1958). "Variation in the Great Horned Owls of Middle America". Auk. 75 (2): 134–142. doi:10.2307/4081882. JSTOR 4081882.
  22. ^ a b c d "Great Horned Owl – Bubo virginianus – Information, Pictures, Sounds". Owlpages.com. Retrieved 2012-02-09.
  23. ^ a b c d e f g h i j Craighead, J. J.; Craighead, F. C. Jr. (1956). Hawks, owls and wildlife. Harrisburg, PA: Stackpole Co. ISBN 0486221237.
  24. ^ a b c d e Snyder, N. F. R.; Wiley, J. W. (1976). "Sexual size dimorphism in hawks and owls of North America". AOU Ornithological Monograph. 20 (20): 1–96. doi:10.2307/40166710. JSTOR 40166710.
  25. ^ Dunning, John B. Jr., ed. (1992). CRC Handbook of Avian Body Masses. CRC Press. ISBN 978-0-8493-4258-5..
  26. ^ a b c d e f g h i Earhart, C. M.; Johnson, N. K. (1970). "Size dimorphism and food habits of North American Owls". Condor. 72 (3): 251–264. doi:10.2307/1366002. JSTOR 1366002.
  27. ^ a b Johnson, D. H. (1998). Duncan, J. R.; Johnson, D. H.; Nicholls, T. H. (eds.). "Wing loading in 15 species of North American owls". Biology and Conservation of Owls of the Northern Hemisphere, 2nd International Symposium, Gen. Tech. Rep. NC-190. St. Paul, MN: U.S. Dept. of Agriculture Forest Service, North Central Forest Experiment Station. 190: 553–561.
  28. ^ "The Silent Flight of Owls, Explained". Audubon. 2017-07-28. Retrieved 2020-02-21.
  29. ^ a b c d e Marti, C. D. (1974). "Feeding ecology of four sympatric owls". Condor. 76 (1): 45–61. doi:10.2307/1365983. JSTOR 1365983.
  30. ^ a b Lee, Carol (March 26, 2006). "Powerful feet and talons help birds of prey make their living". Lubbock Avalanche-Journal. Retrieved 21 March 2013.
  31. ^ Ridgway, Robert (1919). "The birds of North and Middle America: A descriptive catalogue of the higher groups, genera, species, and subspecies of birds known to occur in North America, from the Arctic lands to the Isthmus of Panama, the West Indies and other islands of the Caribbean Sea, and the Galapagos Archipelago pt. 8: Families Jacanidae, Oedicnemidae, Haematopodidae, Arenariidae, Aphrizidae, Charadriidae, Scolopacidae, Phalaropodidae, Recurvirostridae, Rynchopidae, Sternidae, Laridae, Stercorariidae, Alcidae". Bulletin of the United States National Museum (50): i-852. doi:10.5479/si.03629236.50.i.
  32. ^ Norberg, R.A. (1977). "Occurrence in independent evolution of bilateral ear asymmetry in owls and implications in owl taxonomy". Biological Science. London: Philosophical Transaction Royal Society. 280 (973): 375–408. Bibcode:1977RSPTB.280..375N. doi:10.1098/rstb.1977.0116.
  33. ^ Traynor, Robert M. (September 1997). "The missing link for success in hearing aid fittings". The Hearing Journal. 50 (9): 10. doi:10.1097/00025572-199709000-00001. ISSN 0745-7472. S2CID 147068859.
  34. ^ Hall, M. I.; Heesy, C. P. (2011). "Eye size, flight speed and Leuckart's Law in birds". Journal of Zoology. 283 (4): 291–297. doi:10.1111/j.1469-7998.2010.00771.x. S2CID 81153664.
  35. ^ WALEED (2018-08-24). "Great Horned Owl Eyes – How Far Can a Great Horned Owl See?". Great Horned Owl. Retrieved 2020-02-21.
  36. ^ Fite, K. V. (1973). "Anatomical and behavioral correlates of visual acuity in the Great Horned Owl". Vision Research. 13 (2): 219–230. doi:10.1016/0042-6989(73)90101-6. PMID 4692516.
  37. ^ Jacobs, Gerald H.; Crognale, Michael; Fenwick, John (May 1987). "Cone Pigment of the Great Horned Owl". The Condor. 89 (2): 434. doi:10.2307/1368502. JSTOR 1368502.
  38. ^ Miller, A. H. (1934). "The vocal apparatus of some North American owls". Condor. 36 (5): 204–213. doi:10.2307/1363856. JSTOR 1363856.
  39. ^ Morrell, T. E.; Yahner, R. H.; Harkness, W. L. (1991). "Factors affecting detection of Great Horned Owls by using broadcast vocalizations". Wildlife Society Bulletin. 19 (4): 481–488. JSTOR 3782162.
  40. ^ a b c Johnson, D. H. (1993). Spotted Owls, Great Horned Owls, and forest fragmentation in the Central Oregon Cascades (Master's Thesis). Corvallis: Oregon State University.
  41. ^ a b Petersen, L. (1979). "Ecology of Great Horned Owls and Red-tailed Hawks in southeastern Wisconsin". Wisconsin Department of Natural Resources Technical Bulletin. 111.
  42. ^ a b c d e f g h i j Baumgartner, F. M. (1938). "Courtship and nesting of the great horned owls". The Wilson Bulletin: 274–285.
  43. ^ a b c d e f g h i Rohner, C. (1996). "The numerical response of Great Horned Owls to the snowshoe hare cycle: consequences of non-territorial 'floaters' on demography". Journal of Animal Ecology. 65 (3): 359–370. doi:10.2307/5882. JSTOR 5882.
  44. ^ a b "Bird Master Database Search- Bubo virginianus". Florida Museum of Natural History. Retrieved September 23, 2019.
  45. ^ a b Stiles, F. G.; Skutch, A. F. (1989). A guide to the birds of Costa Rica. Ithaca, NY: Comstock Publishing Associates, Cornell University Press. ISBN 0801496004.
  46. ^ a b c Traylor, M. A. (1958). "Variation in South American Great Horned Owls". The Auk. 75 (2): 143–149. doi:10.2307/4081883. JSTOR 4081883.
  47. ^ a b c d Holt, D. W.; Berkley, R.; Deppe, C.; Enríquez Rocha, P. L.; Olsen, P. D.; Petersen, J. L.; Wood, K. L. (1999). "Great Horned Owl". Handbook of Birds of the World, Vol 5. p. 69. ISBN 978-84-87334-25-2.
  48. ^ Dickerman, R. W. (1991). "On the validity of Bubo virginianus occidentalis (Stone)". The Auk. 108: 964–965.
  49. ^ Browning, M. R.; Banks, R. C. (1990). "The identity of Pennant's "Wapacuthu Owl" and the subspecific name of the population of Bubo virginianus from west of Hudson Bay". Journal of Raptor Research. 24: 80–83.
  50. ^ Dickerman, R. W. (1993). "The subspecies of the Great Horned Owls of the central great plains, with notes on adjacent areas". Kansas Ornithology Society Bulletin. 44: 17–21.
  51. ^ a b c d Taverner, P. A. (1942). "Canadian Races of the Great Horned Owls". The Auk. 59 (2): 234–245. doi:10.2307/4079554. JSTOR 4079554.
  52. ^ Bendire, Charles (1892). Smithsonian Contributions to Knowledge: Life Histories of North American Birds. The Smithsonian Institution. p. 383. Retrieved 2012-02-09.
  53. ^ Godfrey, W. E. (1986). The birds of Canada (Revised ed.). Ottawa: National Museum of Natural Sciences. ASIN B003XVMPTC.
  54. ^ Snyder, L. L. (1961). "On an unnamed population of the Great Horned Owl". Ontario Museum, Contribution. 54.
  55. ^ Dickerman, R. W.; Johnson, A. B. (2008). "Notes on Great Horned Owls nesting in the Rocky Mountains, with a description of a new subspecies". Journal of Raptor Research. 42 (1): 20–28. doi:10.3356/JRR-06-75.1. S2CID 84498763.
  56. ^ Howell, S. N. G.; Webb, S. (1995). A guide to the birds of Mexico and northern Central America. New York: Oxford Univ. Press. ISBN 0198540124.
  57. ^ Ridgely, R. S.; Gwynne, J. A. Jr. (1989). A guide to the birds of Panama (2 ed.). Princeton, NJ: Princeton Univ. Press. ISBN 9780691025124.
  58. ^ Flack, J.A.O. (1976). "Bird populations of aspen forests in Western North America". Ornithological Monograph (19): 1–97. doi:10.2307/40166754. JSTOR 40166754.
  59. ^ Mcgarigal, K.; Fraser, J. D. (1984). "The effect of forest stand age on owl distribution in southwestern Virginia". Journal of Wildlife Management. 48 (4): 1393–1398. doi:10.2307/3801804. JSTOR 3801804.
  60. ^ James, D. A.; Neal, J. C. (1986). Arkansas birds: their distribution and abundance. Fayetteville: University of Arkansas Press. ISBN 0938626388.
  61. ^ Morrell, T. E.; Yahner, R. H. (1994). "Habitat characteristics of Great Horned Owls in southcentral Pennsylvania". Journal of Raptor Research (28): 164–170.
  62. ^ a b Smith, D. G.; Murphy, J. R. (1982). "Nest site selection in raptor communities of the Eastern Great Basin Desert". Great Basin Naturalist. 42 (3): 395–404. JSTOR 41711942.
  63. ^ Root, T. (1988). Atlas of wintering North American birds: an analysis of Christmas bird count data. Chicago: University of Chicago Press. ISBN 9780226725406.
  64. ^ Fjeldså, J.; Krabbe, N. (1990). Birds of the high Andes. Svendborg, Denmark: Zoological Museum, University of Copenhagen, and Apollo Books. ISBN 8788757161.
  65. ^ Accordi, I. A.; Barcellos, A. (2006). "Composição da avifauna em oito áreas úmidas da Bacia Hidrográfica do Lago Guaíba, Rio Grande do Sul". Revista Brasileira de Ornitologia. 14 (2): 101–115.
  66. ^ a b Rohner, C.; Krebs, C. J. (1996). "Owl predation on snowshoe hares: consequences of antipredator behaviour". Oecologia. 108 (2): 303–310. Bibcode:1996Oecol.108..303R. doi:10.1007/BF00334655. JSTOR 4221419. PMID 28307843. S2CID 8013050.
  67. ^ Ganey, J. L.; Vojta, S. C. (2005). "Changes in snag populations in northern Arizona mixed-conifer and ponderosa pine forests, 1997–2002". Forest Science. 51 (5): 396–405.
  68. ^ a b Errington, P.L. (1932). "Studies on the Behavior of the Great Horned Owl". Wilson Bulletin. 44 (4): 212–220.
  69. ^ a b Baerg, W. J. (1926). "Trying to Tame a Great Horned Owl". The Auk. 43 (2): 214–217. doi:10.2307/4074915. JSTOR 4074915.
  70. ^ Hume, R. (1991). Owls of the world. Philadelphia, PA: Running Press. ISBN 1561380326.
  71. ^ "Stacey O'Brien : Wesley the Owl: Crows and Ravens: The Corvids and their odd behavior". 2010-04-13.
  72. ^ Baumgartner, F. M. (1939). "Territory and population in the Great Horned Owl". The Auk. 56 (3): 274–282. doi:10.2307/4079048. JSTOR 4079048.
  73. ^ Millard, J. B.; Craig, T. H.; Markham, O. D. (1978). "Cannibalism by an adult Great Horned Owl". Wilson Bulletin. 90 (3): 449.
  74. ^ a b c Houston, C. S. (1978). "Recoveries of Saskatchewan-banded Great Horned Owls". Canadian Field-Naturalist. 92: 61–66.
  75. ^ a b c Smith, D. G.; Murphy, J. R. (1973). "Breeding ecology of raptors in the eastern Great Basin of Utah". Brigham Young University Science Bulletin Biological Services. 18 (3): 1–76.
  76. ^ Fuller, M. R. (1979). Spatiotemporal ecology of four sympatric raptor species (Ph.D.). St. Paul: Univ. of Minnesota.
  77. ^ Packard, R. L. (1954). "Great horned owl attacking squirrel nests" (PDF). The Wilson Bulletin. 66 (4): 272.
  78. ^ Vaughan, T.A. (1954). "Diurnal foraging by the Great Horned Owl". Wilson Bulletin. 66 (2): 148. JSTOR 4158310.
  79. ^ a b Rudolph, S. G. (1978). "Predation Ecology of Coexistng Great Horned and Barn Owls" (PDF). The Wilson Bulletin. 90 (1): 134–137.
  80. ^ Smith, D. G.; Smith, B. A. (1972). "Hunting methods and success of newly-fledged Great Horned Owls". Bird-Banding. 43 (2): 142. doi:10.2307/4511863. JSTOR 4511863.
  81. ^ a b c d e f g h i j k l m n o p q Errington, P. L.; Hamerstrom, F.; Hamerstrom, F. N. Jr. (1940). "The Great Horned Owl and its prey in north-central United States". Iowa Agricultural Express Research Bulletin. 24 (277): 757–850.
  82. ^ a b Orians, G.; Kuhlman, F. (1956). "Red-tailed hawk and horned owl populations in Wisconsin". The Condor. 58 (5): 371–385. doi:10.2307/1365056. JSTOR 1365056.
  83. ^ Einarsen, A. S. (1956). "Determination of some predator species by food signs". Oregon State Monographs. 10: 34.
  84. ^ Longland, W. S.; Price, M. V. (1991). "Direct observations of owls and heteromyid rodents: can predation risk explain microhabitat use?". Ecology. 72 (6): 2261–2273. doi:10.2307/1941576. JSTOR 1941576.
  85. ^ a b c d e f g h Cromrich, L. A.; Holt, D. W.; Leasure, S. M. (2002). "Trophic niche of North American great horned owls". Journal of Raptor Research. 36 (1): 58–65.
  86. ^ a b Murphy, R. K. (1997). "Importance of prairie wetlands and avian prey to breeding Great Horned Owls (Bubo virginianus) in northwestern North Dakota". United States Department of Agricultural, Forest Service General Technical Report: 286–298.
  87. ^ Jaksić, F. M.; Marti, C. D. (1984). "Comparative food habits of Bubo owls in Mediterranean-type ecosystems". The Condor. 86 (3): 288–296. doi:10.2307/1366997. JSTOR 1366997.
  88. ^ a b c d e f g h Smith, Dwight G. (2002). Great Horned Owl (1st ed.). Mechanicsburg, PA: Stackpole Books. pp. 33, 80–81. ISBN 978-0811726894. Retrieved 2013-03-21.
  89. ^ Parmalee, P. W. (1954). "Food of the great horned owl and barn owl in east Texas". The Auk. 71 (4): 469–470. doi:10.2307/4081546. JSTOR 4081546.
  90. ^ Baumgartner, A. M.; Baumgartner, F. M. (1944). "Hawks and owls in Oklahoma 1939-1942: Food habits and population changes". The Wilson Bulletin. 56 (4): 209–215. JSTOR 4157378.
  91. ^ a b c Fitch, H. S. (1947). "Predation by owls in the Sierran foothills of California". The Condor. 49 (4): 137–151. doi:10.2307/1364108. JSTOR 1364108.
  92. ^ Murphy, J. R.; Camenzind, F. J.; Smith, D. G.; Weston, J. B. (1969). "Nesting ecology of raptorial birds in central Utah". Brigham Young University Science Bulletin-Biological Series. 10 (4): 1–36.
  93. ^ Fitch, H. S. (1940). "Some observations on horned owl nests". The Condor. 42 (1): 73–75. doi:10.2307/1364321. JSTOR 1364321.
  94. ^ "Great Horned Owl Menu". Birdnote.org. 2008-08-29. Archived from the original on 2012-03-10. Retrieved 2012-02-09.
  95. ^ a b Powell, B. (1984). Labrador by choice. St. John's, NF: Jesperson Press. ISBN 0920502318.
  96. ^ Eifrig, H. (1909). "Great horned owl versus porcupine". The Auk. 26: 58–59.
  97. ^ Wiley, J.W. (1969). "A Case of Great Horned Owl Predation on a Porcupine". The Condor. 71 (1): 73. doi:10.2307/1366054. JSTOR 1366054.
  98. ^ a b Smith, D. G.; Murphy, J. R. (1979). "Breeding responses of raptors to jackrabbit density in the eastern Great Basin Desert of Utah". Raptor Research. 13: 1–14.
  99. ^ a b Marti, C. D. (1969). "Some comparisons of the feeding ecology of four owls in north-central Colorado". The Southwestern Naturalist. 14 (2): 163–170. doi:10.2307/3668871. JSTOR 3668871.
  100. ^ a b Marti, C. D.; Kochert, M. N. (1996). "Diet and Trophic Characteristics of Great Horned Owls in Southwestern Idaho". Journal of Field Ornithology. 67 (4): 499–506. JSTOR 4514149.
  101. ^ Llinas-Gutirrez, J.; Arnaud, G.; Acevedo, M. (1991). "Food habits of the Great Horned Owl in the Cape Region of Lower California, Mexico". Journal of Raptor Research. 25 (4): 140–141.
  102. ^ a b Adamcik, R. S.; Todd, A. W.; Keith, L. B. (1978). "Demographic and dietary responses of Great Horned Owls during a snowshoe hare cycle". Canadian Field-Naturalist. 92 (2): 156–166. ISSN 0008-3550.
  103. ^ Rohner, C. (1995). "Great Horned Owls and snowshoe hares: what causes the time lag in the numerical response of predators to cyclic prey?". Oikos. 74 (1): 61–68. doi:10.2307/3545675. JSTOR 3545675.
  104. ^ a b c Mcinvaille, W. B. Jr.; Keith, L. B. (1974). "Predator-prey relations and breeding biology of the Great Horned Owl and Red-tailed Hawk in central Alberta". Canadian Field-Naturalist. 88: 1–20.
  105. ^ Weir, D.; Hanson, A. (1989). "Food habits of Great Horned Owls, Bubo virginianus, in the northern taiga of the Yukon Territory and Alaska". Canadian Field-Naturalist. 103: 12–17.
  106. ^ a b Tomazzoni, A. C.; Pedó, E.; Hartz, S. M. (2004). "Food habits of Great Horned Owls (Bubo virginianus) in the breeding season in Lami Biological Reserve, southern Brazil". Ornitologia Neotropical. 15 (2): 279–282. S2CID 90637198.
  107. ^ Wink, J.E.; Senner, S. E.; Goodrich, L. J. (1987). "Food habits of great horned owls in Pennsylvania". Proceedings of the Pennsylvania Academy of Science. 61 (2): 133–137. JSTOR 44111738.
  108. ^ Burns, B. J. (1952). "Food of a Family of Great Horned Owls, Bubo virginianus, in Florida". The Auk. 69 (1): 86–87. doi:10.2307/4081300. JSTOR 4081300.
  109. ^ Baker, J. K. (1962). "The manner and efficiency of raptor depredations on bats". The Condor. 64 (6): 500–504. doi:10.2307/1365473. JSTOR 1365473.
  110. ^ Kittredge, V. C.; Wilson, P. W.; Caire, W. (2007). "An updated checklist of the food items of the great horned owl (Bubo virginianus: Strigiformes: Strigidae) in Oklahoma". Proceedings- Oklahoma Academy of Science. 86.
  111. ^ Twente, J. W. (1954). "Predation on bats by hawks and owls". The Wilson Bulletin. 66 (2): 135–136.
  112. ^ Bull, E. L.; Heater, T. W. (2001). "They may go for Pine Martens as a prey item, but the marten will fight back hard". Northwestern Naturalist: 1–6. doi:10.2307/3536640. JSTOR 3536640.
  113. ^ Mendall, H. L. (1944). "Food of Hawks and Owls N Maine". The Journal of Wildlife Management. 8 (3): 198–208. doi:10.2307/3795698. JSTOR 3795698.
  114. ^ Brown, L. N. (1997). A guide to the mammals of the southeastern United States. University of Tennessee Press. ISBN 0870499661.
  115. ^ Storm, G. L.; Andrews, R. D.; Phillips, R. L.; Bishop, R. A.; Siniff, D. B.; Tester, J. R. (1976). "Morphology, reproduction, dispersal, and mortality of midwestern red fox populations". Wildlife Monographs (49): 3–82. JSTOR 3830425.
  116. ^ a b Ray, J.D. (2012). "Great Silent Hunter". Birdwatching Magazine. Braintree, Massachusetts.
  117. ^ Sovada, M. A.; Roy, C. C.; Bright, J. B.; Gillis, J. R. (1998). "Causes and rates of mortality of swift foxes in western Kansas". The Journal of Wildlife Management. 62 (4): 1300–1306. doi:10.2307/3801994. JSTOR 3801994.
  118. ^ Kilgore, D.L. (1969). "An ecological study of the swift fox (Vulpes velox) in the Oklahoma panhandle". American Midland Naturalist. 81 (2): 513–534. doi:10.2307/2423986. JSTOR 2423986.
  119. ^ Bosakowski, T.; Speiser, R.; Smith, D. G. (1989). "Nesting ecology of forest-dwelling Great Horned Owls in the Eastern Deciduous Forest Biome". Canadian Field-Naturalist. 103: 65–69.
  120. ^ "Blakeman answers questions about nest maintenance". Blakeman on Hawks. Retrieved 6 July 2005.
  121. ^ Roger A. Powell, Martes pennanti, Mammalian Species, Issue 156, 8 May 1981, Pages 1–6, https://doi.org/10.2307/3504050
  122. ^ Axelson, G. (2012). Fewer Fishers in the Forest. Minnesota Department of Natural Resources.
  123. ^ Olson, Karen (January 19, 2011). "Chihuahua survives owl attack in Illinois". CNN. Retrieved 21 March 2013.
  124. ^ Johansson, Tait. "The Great Horned Owl". Bedford Audubon Society. Archived from the original on 2012-03-20. Retrieved 2012-02-09.
  125. ^ Deal, K. (2010). Wildlife and Natural Resource Management. Cengage Learning. ISBN 9781305627741.
  126. ^ "Beware of the Great Horned Owl". Help Find Lost Pets. May 27, 2010. Archived from the original on 3 March 2012. Retrieved 21 March 2013.
  127. ^ "Great Horned Owl – Bubo virginianus". Raptor Education Center. Retrieved 21 March 2013.
  128. ^ Forbush, Edward H. "The Great Horned Owl (1927)." The Essential Naturalist: Timeless Readings in Natural History (2011): 15.
  129. ^ Huey, L. M. (1931). "Skunks as Prey for Owls" (PDF). The Wilson Bulletin: 224.
  130. ^ Hunter, Luke (2011). Carnivores of the World. Princeton, NJ: Princeton University Press. ISBN 9780691152288.
  131. ^ a b Crocoll, S. T. (1984). Breeding biology of broad-winged and red-shouldered hawks in western New York (Doctoral dissertation). State University of New York at Fredonia, Department of Biology.
  132. ^ a b Errington, P. L. (1932). "Food habits of southern Wisconsin raptors. Part I. Owls". The Condor. 34 (4): 176–186. doi:10.2307/1363563. JSTOR 1363563.
  133. ^ Hamerstrom, F. N. (1939). "A study of Wisconsin prairie chicken and sharp-tailed grouse". The Wilson Bulletin. 51 (2): 105–120. JSTOR 4156820.
  134. ^ Keith, L. B.; Rusch, D. H. (1988). "Predation's role in the cyclic fluctuations of Ruffed Grouse". Proceeding International Congress of Ornithology. 19: 699–732.
  135. ^ a b Hayward, J. L.; Galusha, J. G.; Frias, G. (1993). "Analysis of Great Horned Owl pellets with Rhinoceros Auklet remains". The Auk. 110 (1): 133–135.
  136. ^ Schemnitz, S. D.; Goerndt, D. L.; Jones, H. (1985). "Habitat needs and management of Merriam's turkeys in southcentral New Mexico". Proceedings of National Wild Turkey Symposium. 5: 199–232.
  137. ^ a b "Great Horned Owl | the Peregrine Fund".
  138. ^ König, Claus, Friedhelm Weick, and Jan-Hendrik Becking. Owls of the World. 2nd ed. Bloomsbury Publishing, 2009. Web. 23 May. 2023.
  139. ^ Monnie, J. B. (1966). "Reintroduction of the Trumpeter Swan to its former prairie breeding range". Journal of Wildlife Management. 30 (4): 691–696. doi:10.2307/3798274. JSTOR 3798274.
  140. ^ Knopf, F. L.; Evans, R. M. (2020). "American White Pelican (Pelecanus erythrorhynchos), version 1.0". In Poole, A. F. (ed.). Birds of the World. Ithaca, NY, USA: Cornell Lab of Ornithology. doi:10.2173/bow.amwpel.01. S2CID 216485857.
  141. ^ Schreiber, R. W.; Risebrough, R. W. (1972). "Studies of the Brown Pelican". The Wilson Bulletin. 84 (2): 119–135. JSTOR 4160189.
  142. ^ Littlefield, C. D. (2003). "Sandhill Crane nesting success and productivity in relation to predator removal in southeastern Oregon". The Wilson Bulletin. 115 (3): 263–269. doi:10.1676/02-108. JSTOR 4164569. S2CID 86244240.
  143. ^ Toland, B. (1991). "Great horned owl predation of Atlantic loggerhead turtle hatchlings". Florida Field Naturalist. 19: 117–119.
  144. ^ Duncan, J.R.; Lane, P.A. (1998). "Great Horned Owl Observed Hawking "Insects"". Journal of Raptor Research. 22 (3): 93.
  145. ^ Errington, P. L. (1938). "The Great Horned Owl as an indicator of vulnerability in prey populations". The Journal of Wildlife Management. 2 (4): 190–205. doi:10.2307/3795666. JSTOR 3795666.
  146. ^ Mona, K. "Great Horned Owl on Motion Camera". Twin Cities Naturalist. Retrieved 2016-11-29.
  147. ^ a b Hindmarch, Sofi; Elliott, John E. (2015-02-04). "Comparing the diet of Great Horned Owls (Bubo virginianus) in rural and urban areas of southwestern British Columbia". The Canadian Field-Naturalist. 128 (4): 393. doi:10.22621/cfn.v128i4.1634. ISSN 0008-3550.
  148. ^ a b Kopij, G (2012). "Food niche overlap in co-existing Barn Owl Tyto alba (Scopoli 1769) and Great Horned Owl Bubo virginianus Gmelin 1788 in intensively used farmland". Pol. J. Ecol. 61: 179–181.
  149. ^ Rullman, Stan; Marzluff, John M. (2014). "Raptor Presence Along an Urban–Wildland Gradient: Influences of Prey Abundance and Land Cover". Journal of Raptor Research. 48 (3): 257–272. doi:10.3356/jrr-13-32.1. ISSN 0892-1016. S2CID 86034385.
  150. ^ Chace, Jameson F.; Walsh, John J. (2006). "Urban effects on native avifauna: a review". Landscape and Urban Planning. 74 (1): 46–69. doi:10.1016/j.landurbplan.2004.08.007.
  151. ^ Lambert, Anthony (1981). "Presence and Food Preferences of the Great Horned Owl in the Urban Parks of Seattle". The Murrelet. 62 (1): 2–5. doi:10.2307/3534439. JSTOR 3534439.
  152. ^ Stone, Ward B.; Okoniewski, Joseph C.; Stedelin, James R. (April 1999). "Poisoning of Wildlife with Anticoagulant Rodenticides in New York". Journal of Wildlife Diseases. 35 (2): 187–193. doi:10.7589/0090-3558-35.2.187. ISSN 0090-3558. PMID 10231745. S2CID 22823380.
  153. ^ WLM. (1918). Bird Enemies of the Varying Hare. The Auk, 372-373.
  154. ^ Bibles, Brent D., Richard L. Glinski and R. Roy Johnson. 2002. Gray Hawk (Buteo plagiatus), The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology.
  155. ^ Dunstan, T. C., & Harrell, B. E. (1973). Spatio-temporal relationships between breeding red-tailed hawks and great horned owls in South Dakota. Raptor Research, 7(2), 49–54.
  156. ^ Barrows, C. W. (1989). Diets of five species of desert owls. Western Birds, 20(1), 1-10.
  157. ^ a b Duncan, J. R. 1987. Movement strategies, mortality, and behavior of radio-marked Great Gray Owls in southeastern Manitoba and northern Minnesota. Pages 101-107 in Biology and conservation of northern forest owls: Symposium proceedings, February 3–7, Winnipeg, MB. (Nero, R. W., R. J. Clark, R. J. Knapton, and R. H. Hamre, Eds.) General Technical Report, RM-142. Fort Collins, CO: USDA, Forest Service, Rocky Mountain Forest and Range Experiment Station.
  158. ^ Rohner, C., Smith, J. N., Stroman, J., Joyce, M., Doyle, F. I., & Boonstra, R. (1995). Northern hawk-owls in the nearctic boreal forest: prey selection and population consequences of multiple prey cycles. Condor, 208-220.
  159. ^ Forsman, E. D., Anthony, R. G., Reid, J. A., Loschl, P. J., Sovern, S. G., Taylor, M., & Seaman, D. E. (2002). Natal and breeding dispersal of northern spotted owls. Wildlife Monographs, 1-35.
  160. ^ Stoleson, S. H., & Sadoti, G. (2010). Zone-tailed Hawk (Buteo albonotatus). In: Cartron, Jean-Luc, ed. Raptors of New Mexico. Albuquerque, NM: University of New Mexico Press.
  161. ^ Sutherland, J. E. 1987. The predation ecology of the Northern Harrier (Circus cyaneus hudsonius) on Mallard Island, North Dakota. Master's Thesis. Univ. of N. Dakota, Grand Forks.
  162. ^ Bechard, Marc J. and Josef K. Schmutz. 1995. Ferruginous Hawk (Buteo regalis), The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology.
  163. ^ Dawson, J. W., & Mannan, R. W. (1991). The role of territoriality in the social organization of Harris' Hawks. The Auk, 661-672.
  164. ^ Steidl, R. J., & Griffin, C. R. (1991). Growth and brood reduction of mid-Atlantic coast ospreys. The Auk, 363-370.
  165. ^ Walton, B. J., & Thelander, C. G. (1988). Peregrine falcon management efforts in California, Oregon, Washington, and Nevada. Peregrine falcon populations: their management and recovery. The Peregrine Fund, Boise, Idaho, USA, 587-598
  166. ^ Boal, C. W., & Mannan, R. W. (1994). Northern goshawk diets in ponderosa pine forests on the Kaibab Plateau. Studies in Avian Biology, 16, 97-102.
  167. ^ Cold, C. W. 1993. Adult male osprey killed at nest by Great Horned Owl. Passenger Pigeon 55:269-270.
  168. ^ Rohner, C. and F. I. Doyle. 1992. Food-stressed Great Horned Owl kills adult goshawk: exceptional observation or community process? Journal of Raptor Research, 26:261-263.
  169. ^ Bechard, Marc J. and Theodor R. Swem. 2002. Rough-legged Hawk (Buteo lagopus), The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology.
  170. ^ Rohner, C., Krebs, C. J., Hunter, D. B., & Currie, D. C. (2000). Roost site selection of great horned owls in relation to black fly activity: an anti-parasite behavior? The Condor, 102(4), 950-955.
  171. ^ Houston, C. S. and K. A. Wylie. 1985. Peregrine Falcons harass nesting Great Horned Owls. Blue Jay 43:42-43.
  172. ^ Cully, J. F., & Ligon, J. D. (1976). Comparative mobbing behavior of scrub and Mexican jays. The Auk, 116-125.
  173. ^ Ohlendorf, H. M. (1974). Competitive relationships among kingbirds (Tyrannus) in trans-Pecos Texas. Wilson Bulletin, 86(4), 357-373.
  174. ^ "These Owl Chicks Have Two Moms and a Dad—a First". 2018-05-02.
  175. ^ Morse, Douglass H. (April 1971). "Great Horned Owls and Nesting Seabirds". The Auk. 88 (2): 426–427. doi:10.2307/4083889. ISSN 0004-8038. JSTOR 4083889.
  176. ^ WALEED (2018-08-29). "Great Horned Owl Nest – Interesting Facts & Information". Great Horned Owl. Retrieved 2020-02-21.
  177. ^ Mader, W. J. 1973. Notes on nesting Great Horned Owls in southern Arizona. Raptor Research, 7:109-111.
  178. ^ Bendire, C. E. 1892. Life histories of North American birds with special reference to their breeding habits and eggs. Smithsonian Contributions to Knowledge 28:376-389.
  179. ^ Burkholder, G. & Smith, D.G. 1988. Great Horned Owl (Bubo virginianus) nesting in a Great Blue Heron (Ardea herodias) heronry. Journal of Raptor Research, 22 (2): 62.
  180. ^ Smith, D. G. 1969. Nesting ecology of the Great Horned Owl, Bubo virginianus. Brigham Young University Science Bulletin Biological Services, 10(4):16-25.
  181. ^ Austing, G. R. 1968. The owls and I. Audubon 70:72-79.
  182. ^ Peck, G. K. and R. D. James. 1983. Breeding birds of Ontario: nidiology and distribution. Vol. 1. Royal Ontario Museum, Toronto.
  183. ^ a b Turner, Jr., J. C. and L. McClanahan, Jr. 1981. Physiogenesis of endothermy and its relation to growth in the Great Horned Owl, Bubo virginianus. Compilation of Biochemical Physiology, 68A:167-173.
  184. ^ a b Hoffmeister, D. F. and H. W. Setzer. 1947. The postnatal development of two broods of Great Horned Owls (Bubo virginianus). University of Kansas Publishing Museum of Natural History, 1:157-173.
  185. ^ Sumner, Jr., E. L. 1934. The behavior of some young raptorial birds. University of California, Publication on Zoology, 40:331-362.
  186. ^ Dunstan, T. C. 1970. Post-fledging activities of juvenile Great Horned Owls as determined by radio-telemetry. Ph.D. thesis. University of South Dakota, Vermillion.
  187. ^ Fuller, M. R. 1979. Spatiotemporal ecology of four sympatric raptor species. Ph.D. thesis. University of Minnesota, St. Paul.
  188. ^ Houston, C.S. 1971. Brood size of Great Horned Owls in Saskachetwan. Bird-Banding, 42:103-105.
  189. ^ Weller, M. W. 1965. Bursa regression, gonad cycle and molt of the Great Horned Owl. Bird-Banding 36:102-112.
  190. ^ a b Smith, D. (1999). "Nest Site Selection by Urban and Rural Great Horned Owls in the Northeast (Selección del Lugar de Anidamiento por Parte de Bubo Virginianus en Zonas Urbanas y Rurales del Nordeste de los Estados Unidos)". Journal of Field Ornithology. 70 (4): 535–542. JSTOR 4514446 – via JSTOR.
  191. ^ Minor, William, Minor, Maureen & Ingraldi, Michael (1993). "Nesting of Red-Tailed Hawks and Great Horned Owls in a Central New York Urban/Suburban Area (Anidamiento de Buteo jamaicensis y de Bubo virginianus en un area urbana/suburbana de la parte central de New York". Journal of Field Ornithology. 4 (4): 433–439. JSTOR 4513852 – via JSTOR.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  192. ^ Stout, William E. (2008). "Early breeding records and nesting phenology of Great Horned Owls in Wisconsin". The Passer Pigeon. 70: 381–388.
  193. ^ Artuso, Christian (2007-03-01). "January initiation of suburban great horned owl nests in Manitoba". Blue Jay. 65 (1). doi:10.29173/bluejay5871. ISSN 2562-5667.
  194. ^ Nero, R. W. 1992. New Great Horned Owl longevity record. Blue Jay 50:91-92.
  195. ^ Sky, Big (2016-10-10). "Interesting Facts About Great Horned Owls". Visit Big Sky, Montana. Retrieved 2020-02-21.
  196. ^ Garcelon, D. K. 1981. Mortality of Great Horned Owls associated with skunks. Murrelet 62:26.
  197. ^ Peterson, R. T. 1968. The Birds. Time-Life International (Nederland).
  198. ^ Perry, R. W., Brown, R. E., & Rudolph, D. C. (2001). Mutual mortality of great horned owl and southern black racer: a potential risk of raptors preying on snakes. The Wilson Bulletin, 113(3), 345-347.
  199. ^ Herbert, R. A., & Herbert, K. G. S. (1965). Behavior of peregrine falcons in the New York City region. The Auk, 62-94.
  200. ^ Stewart, P. A. (1969). Movements, population fluctuations, and mortality among great horned owls. The Wilson Bulletin, 155-162.
  201. ^ Olendorff, R. R., Miller, A. D., & Lehman, R. N. (1981). Suggested practices for raptor protection on powerlines: the state of the art in 1981 (No. 4). Published and distributed for the Edison Electric Institute by Raptor Research Foundation.
  202. ^ Mendenhall, V. M. and L. F. Pank. 1980. Secondary poisoning of owls by anticoagulant rodenticides. Wildlife Society Bulletin, 8:311-315.
  203. ^ Cheney, C. D., S. B. Vander Wall, and R. J. Poehlmann. 1987. Effects of strychnine on the behavior of Great Horned Owls and Red-tailed Hawks. Journal of Raptor Research, 21:103-110.
  204. ^ Seidensticker IV, J. C. and H. V. Reynolds III. 1971. The nesting, reproductive performance, and chlorinated hydrocarbon residues in the red-tailed hawk and Great Horned Owl in southcentral Montana. Wilson Bulletin, 83:408-418.
  205. ^ Blus, L. J. 1996. Effects of pesticides on owls in North America. Journal of Raptor Research, 30:198-206.
  206. ^ Buck, J. A., L. W. Brewer, M. J. Hooper, G. P. Cobb, and R. J. Kendall. 1996. Monitoring Great Horned Owls for pesticide exposure in southcentral Iowa. Journal of Wildlife Management, 60:321-331.
  207. ^ Keith, J. A. and I. M. Gruchy. 1972. Residue levels of chemical pollutants in North American birdlife. Proceedings of International Congregation of Ornithology, 15:437-452.
  208. ^ Barrows, W. B. 1912. "Michigan bird life". Michigan Agricultural College, Lansing.
  209. ^ Cade, T. J., P. T. Redig, and H. B. Tordoff. 1989. Peregrine Falcon restoration: Expectation vs. reality. Loon 61:160-162.
  210. ^ Forsman, E. D., E. C. Meslow, and H. M. Wight. 1984. Distribution and biology of the Spotted Owl in Oregon. Wildlife Monographs, 87.
  211. ^ Brylski, P., Hays, L., & Avery, J. (1998). Recovery Plan for the Pacific Pocket Mouse, Perognathus longimembris pacificus. U.S. Fish & Wildlife Service.
  212. ^ Grinnell, J. (1932). Habitat relations of the giant kangaroo rat. Journal of Mammalogy, 13(4), 305-320.
  213. ^ Kelt, D. A., Wilson, J. A., & Konno, E. S. (2005). Differential response of two kangaroo rats (Dipodomys) to the 1997-1998 El Niño southern oscillation event. Journal of Mammalogy, 86(2), 265-274.
  214. ^ Breck, S. W., Biggins, D. E., Livieri, T. M., Matchett, M. R., & Kopcso, V. (2006). Does Predator Management Enhance Survival of Reintroduced Black-footed Ferrets? Recovery of the black-footed ferret-progress and continuing challenges, 203-209.
  215. ^ Berger, D. D., Hamerstrom, F., & Hamerstrom Jr, F. N. (1963). The effect of raptors on prairie chickens on booming grounds. The Journal of Wildlife Management, 778-791.
  216. ^ Hagen, C. A., Pitman, J. C., Sandercock, B. K., Robel, R. J., & Applegate, R. D. (2007). Age‐Specific Survival and Probable Causes of Mortality in Female Lesser Prairie‐Chickens. The Journal of wildlife management, 71(2), 518-525.
  217. ^ Nelson, S. K., & Hamer, T. E. (1995). Nest success and the effects of predation on marbled murrelets. Ecology and Conservation of the Marbled Murrelet. USDA Forest Service General Technical Report PSW-GTR-152. Pacific Southwest Research Station, Albany, CA, 89-98.
  218. ^ Woolfenden, Glen E. and John W. Fitzpatrick. 1996. Florida Scrub-Jay (Aphelocoma coerulescens) , The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology
  219. ^ Balda, R. P., & Bateman, G. C. (1971). Flocking and annual cycle of the pinon jay, Gymnorhinus cyanocephalus. Condor, 287-302.
  220. ^ Mayfield, Harold F. 1992. Kirtland's Warbler (Setophaga kirtlandii), The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology
  221. ^ Chipley, R.M., Fenwick, G.H., Parr, M.J. & Pashley, D.M., editors, 2003. The American Bird Conservancy Guide to the 500 Most Important Bird Areas in the United States: Key Sites for Birds and Birding in All 50 States. Random House Trade Paperbacks, ISBN 0812970365.
  222. ^ "Great Horned Owl (Bubo virginianus)". Alberta Environment & Parks.
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Great horned owl: Brief Summary ( англиски )

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The great horned owl (Bubo virginianus), also known as the tiger owl (originally derived from early naturalists' description as the "winged tiger" or "tiger of the air"), or the hoot owl, is a large owl native to the Americas. It is an extremely adaptable bird with a vast range and is the most widely distributed true owl in the Americas. Its primary diet is rabbits and hares, rats and mice, and voles, although it freely hunts any animal it can overtake, including rodents and other small mammals, larger mid-sized mammals, birds, reptiles, amphibians, and invertebrates. In ornithological study, the great horned owl is often compared to the Eurasian eagle-owl (Bubo bubo), a closely related species, which despite the latter's notably larger size, occupies the same ecological niche in Eurasia, and the red-tailed hawk (Buteo jamaicensis), with which it often shares similar habitat, prey, and nesting habits by day, thus is something of a diurnal ecological equivalent. The great horned owl is one of the earliest nesting birds in North America, often laying eggs weeks or even months before other raptorial birds.

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Granda kornostrigo ( есперанто )

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La granda kornostrigovirginia kornostrigo, Bubo virginianus, estas specio de granda birdo el la ordo de strigoformaj, familio de strigedoj, kun granda plumtufo super ĉiu okulo. Ĝi estas indiĝena de Norda kaj Suda Ameriko. Ĝi estas adaptema birdo kun ampleksa teritorio, kvankam ne tiom disvastigata kiom tiu de la Turstrigo.

Disvastiĝo

La reprodukta vivejo de la granda kornostrigo disvastiĝas tra Nordameriko kaj Sudameriko. Ene de ties biotopo ili povas loĝi ĉe arboj kiuj inkludas deciduajn, koniferajn kaj miksitajn arbarojn, tropikajn pluvarbarojn, pampojn, herbejojn, montajn areojn, dezertojn, subarktan tundron, rokajn marbordojn, mangrovojn kaj kelkajn urbajn areojn. Kvankam mal pli komuna en la plej ekstremaj areoj (ekz., en la centro de dezertoj, plej densaj pluvarbaroj, ktp.) kaj malesta ĉe la alta arkta tundro, ili troviĝas en plej parto de biotopoj.

Aspekto

La granda kornostrigo estas el 46 ĝis 68 cm longa kaj havas enverguron de 101 ĝis 153 cm. Mezaveraĝa granda kornostrigo estas 55 cm longa, havas enverguron de 124 cm kaj pezas ĉirkaŭ 1400 g. Ĝenerale, la plej grandaj kornostrigoj troviĝas proksime de la polusaj regionoj kaj la plej malgrandaj proksime de la Ekvatoro. Inoj estas pli grandaj ol maskloj. Plenkreskuloj havas grandajn oreltufojn, ruĝecan, brunan aŭ grizan vizaĝon limigitan de nigra bordo kaj kun nigra beko centre kaj blankan makulon en la gorĝo. La irisoj estas flavaj, escepte en la raso B. v. nacurutu ĉe kiuj ĝi estas sukcenkolora. La oreltufoj ne estas vere oreloj, sed simple plumotufoj. La subaj partoj estas helaj kun bruna horizontala striado; la supraj partoj estas makulitaj je bruno. La kruroj kaj piedoj estas kovritaj el plumoj ĝis la kalkanoj.

Estas individuaj kaj regionaj varioj laŭ koloro; birdoj el sub-Arkto estas malpli striitaj, helsablokoloraj, dum tiuj de Centrameriko povas esti malhele ĉokoladbrunaj. Tiuj strigoj havas ankaŭ spektaklan duokulan vidkapablon necesa por lokigi eventualjn predojn kaj vidi en malhelo. Strigoj ne povas movi siajn okulojn kiel homoj ekzemple. Tiuj estas enfermitaj en speciala cirkla osto. Tamen, iliaj koloj povas turniĝi 270 gradojn por vidi en aliaj direktoj sen movi siajn enterajn korpojn. La aŭdkapablo de tiuj strigoj estas tiom bonkvalita —se ne pli bone— ol ilia vidkapablo. Tiu strigoj havas sterean aŭdkapablon, kiu permesas ilin trovi la precizan lokon de iliaj predoj. Tiuj birdoj havas ankaŭ tre fortajn kalkanojn.

Reproduktado

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La granda kornostrigo

La granda kornostrigo estas inter la plej fruaj reproduktantoj de Nordameriko. Ili reproduktiĝas en malfrua januaro aŭ frua februaro kaj ofte oni aŭskultas ilin alvokante unu la alian aŭtune, komencante en oktobro. Ili elektas partneron ĉirkaŭ decembro kaj ofte ili estas aŭdataj duope antaŭ tiu epoko. Ĉ estrigoj de pli tropikaj klimatoj, la datoj de reprodukta sezono estas iom necerta. Ili ofte uzas neston uzitan de aliaj granda birdo, foje aldonante plumojn por kovri la neston, sed kutime ne multe pli. Ili preferas nestojn de korvoj, korakoj kaj de jamajka buteo aŭ de grandaj sciuroj en Nordameriko. Tamen, ili tute ne dependas el oldaj nestoj de aliaj specioj, sed male ili povas uzi truojn en arboj kaj stumpoj, klifoj, abandonitaj konstruaĵoj kaj eĉ artefaritaj platformoj.

Kutime estas 2 ovojn en ĉiu ovodemetado, sed la kvanto povas varii el 1 ĝis 5 ovoj (5 estas tre rara). La mezaveraĝa ovolarĝo estas 46.5 mm, la mezaveraĝa longo estas 55.2 mm kaj la mezaveraĝa pezo estas 51 g. La kovado daŭras el 30 ĝis 37 tagojn, mezaveraĝe 33 tagojn. Kovado estas preskaŭ konstanta ĝis kiam la idoj estas 2semajnaĝaj. La strigidoj moviĝas al proksimaj branĉoj je 6 semajnoj kaj ekflugas post ĉirkaŭ unu semajno plia. Oni vidis idojn petante manĝon eĉ en malfrua oktobro (5 monatoj post elnestiĝo) kaj plej parto ne separiĝas el siaj gepatroj preskaŭ ĝis kiam tiuj komencas reproduktiĝi denove (kutime decembro). La birdoj povas ne reproduktiĝi dum alia jaro aŭ eĉ dua kaj estas ofte vagantoj ĝis kiam ili setlas siajn proprajn teritoriojn.

Ĉiu plenkreskulo de granda kornostrigo estas konstanta loĝanto de sia teritorio. Ovoj, idoj kaj junuloj povas esti predataj de vulpoj, kojotoj, katoj. Preskaŭ ne estas predantoj de plenkreskuloj, sed ili povas esti mortigitaj en luktoj kontraŭ agloj, neĝostrigoj kaj, ĉefe, kontraŭ alia granda kornostrigo, kio povas finiĝi en manĝo de la ĵus mortinta strigo.

Ĉasado kaj kutimaro

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La granda kornostrigo dumfluge (komponaĵo)

Tiuj nearktisaj kaj neotropisaj birdoj ĉasas dumnokte per gvatado sur alta gvatejo kaj falŝvebante super la predo. Tiu povas esti tre varia, sed ĉefe el malgrandaj al mezgrandaj mamuloj kiel ratoj, sciuroj, muŝoj, talpoj, kamporatoj, marmotoj, mefitoj, sorikoj, vespertoj, musteloj, gerboj kaj eĉ histrikoj. Iuloke leporoj kaj kunikloj povas konsistigi la plej parton de la manĝobezono de Grandaj kornostrigoj. Birdoj konsistigas la alian grandan parton de la predoj de la Granda kornostrigo, kun birdogrando el regolo ĝis Herodiardeo. Iuloke, akvobirdoj, ĉefe fulikoj kaj anasoj, povas esti gravaj predoj; tiuj strigoj povas predi ankaŭ rabobirdojn gsix la grando de neĝostrigo. Reptilioj, amfibioj, fiŝoj, krustulojn kaj eĉ insektoj povas esti eventualaj predoj. En nordaj regionoj, kie pli grandaj predoj ne povas esti manĝataj rapide, ili povas lasi nemanĝitan manĝaĵon frostitan kaj poste varmigi ĝin per sia propra korpa varmo. Ili kutime manĝas kaj vomas manĝaĵon en la samaj lokoj.

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Vizaĝo de granda kornostrigo

Ili havas elstarajn aŭdkapablon kaj vidkapablon en malforta lumo. La aŭdkapablo estas multe pli pova ol tiu homa kaj same la percepto de la sonaltiĝo. Tio lasta eblas ĉar la oreloj de la strigoj ne estas samloke en ambaŭ flankoj de la kapo: la dekstra orelo estas tipe pli alta en la kranio kaj je ioma diferenca angulo. Movante aŭ turnante sian kapon ĝis la sono estas sama en ĉiu orelo, strigo povas lokigi kaj la horizontalan kaj la vertikalan direkton de sono. La okuloj de la Granda kornostrigo estas preskaŭ tiom grandaj kiom tiuj homaj kaj estas nemoveblaj en siaj ingoj. Anstataŭ turni siajn okulojn, la strigo turnas sian kapon.

La alvoko estas altatona sed laŭta "ho-ho-hu hu hu." Foje estas nur kvar silaboj anstataŭ kvin. La alvoko de la ino estas pli alta kaj laŭtiĝas fine de la alvoko. Junuloj povas produkti susurajn aŭ kriĉajn sonojn kiuj ofte povas esti konfuzitaj kun tiuj de la Turstrigo. La alvoko de la masklo estas ofte uzata en holivudaj filmoj, nedepende de kiu strigo aperas surekrane (simila al krio de jamajka buteo).

La Granda kornostrigo estas la oficiala birdo de Alberto. La Granda kornostrigo povas facile esti konfuzita kun la Bubo magellanicus, la Magelana kornostrigo (kiu iam estis konsiderata kiel apartenanta al tiu ĉi specio), kaj kun aliaj gufoj aŭ gufoj.

Subspecioj

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Vizaĝo kaj brusto (kun blanka makulo) de granda kornostrigo
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Granda kornostrigo

Estis nomita granda nombro de subspecioj. Kiel dirite supre, multaj al tiuj estas nur ekzemploj de individuoj aŭ klina variado. Diferencoj inter subspecioj estas ĉefe pri koloro kaj grando kaj ĝenerale sekvas la regulojn de Gloger kaj Bergmann.

  • B. v. virginianus (Gmelin, 1788): Komuna granda kornostrigo
Usono orienten el Minesoto al orienta Teksaso; nordorienten al Nova Skotio kaj Insulo de Princo Eduardo, Kanado. Loĝanta la tutan jaron.
Bruna formo, nuance ruĝeca kaj striita distinge nigrebrune sube. Sablokoloraj piedoj, ofte striitaj nigre.
Formo el malaltaj teroj en disaj loĝantaroj el orienta Kolombio al la Gujanoj; ankaŭ el Bolivio kaj Brazilo sude de Amazonio al norda Argentino; loĝanta la tutan jaron. Ĝi inkludas la proponitajn subspeciojn scotinus, elutus, kaj deserti (Holt et al. 1999). La statuso de tiu formo, ĉefe la rilatoj inter la subloĝantaroj kaj kun la ssp. nigrescens kaj kun la magelana kornostrigo, bezonas pli da studo.
Bruneca kun longa beko; birdoj el duonseka interno de Brazilo ofte havas multe pli da blanko en supra vosto kaj orelkovriloj. Ĝi estas la ununura subspecio kie la iriso estas sukcenkolora, ne flava.
  • B. v. subarcticus Hoy, 1852: Norda granda kornostrigo
Reprodukta teritorio el Makenzio kaj nordorienta Brita Kolumbio orienten al Hudsona Golfo; suda limo ne estas klara sed almenaŭ atingas al Montano kaj Norda Dakoto. Nereproduktuloj troviĝas ofte sude de latitudo 45°S, eventuale transen. La taksono inkludas la birdojn priskribitajn kiel occidentalis (sed vidu sube), kaj sclariventris (Dickerman 2004). La olda nomo wapacuthu estis foje uzita por tiu subspecio, sed ĝi ne povas certige esti uzata por rekonebla taksono kaj devas esti konsiderita nomen dubium (duba nomo). La loĝantaro priskribita kiel algistus estas probable bazita sur vagantaj individuoj aŭ intergraduloj de subarcticus, saturatus kaj lagophonus.(Holt et al. 1999)
Pala formo, ĉefe blankeca kun sablokolora nuanco; nigra striado supre varia el nedistinga al akcenta. Tre palaj birdoj estas similaj al junaj inoj de Neĝostrigo vidataj de malproksime. Piedoj blankecaj al sablokoloraj, kun malmulta aŭ nenia bildo.
  • B. v. pacificus Cassin, 1854: Kalifornia granda kornostrigo
Centra kaj suda Kalifornio okcidente de Sierra Nevada escepte la Valo San Joaquin, sude al nordokcidenta Baja California, Meksiko. Intergraduloj kun pallescens en Kantono San Diego, Kalifornio (vidu ankaŭ sube). Loĝanta la tutan jaron.
Tre brunaj, malhele striita sube distinga, sed malpli akcenta ol ĉe saturatus. Nigraj ŝultroj. Piedoj punktitaj je malhela.
  • B. v. saturatus Ridgway, 1877: Marborda granda kornostrigo
Marbordo de Pacifiko el sudorienta Alasko al norda Kalifornio. Loĝanta la tutan jaron.
Malhela, sablokolora kaj iome grizeca formo kun tre forta striado sube. Piedoj preskaŭ malhelaj.
  • B. v. nigrescens Berlepsch, 1884: Nordanda granda kornostrigo
Andoj; sekaj zonoj kaj punao el Kolombio al nordokcidenta Peruo. Loĝanta la tutan jaron.
Malhela, grizbruna formo kun tre malhelaj grizbrunaj punktetoj.
  • B. v. pallescens Stone, 1897: Dezerta granda kornostrigo
Valo San Joaquin sudorienten tra sekaj regionoj de sudorienta Kalifornio kaj suda Utaho orienten al okcidenta Kansaso kaj suden al Guerrero kaj okcidenta Veracruz en Meksikio; intergraduloj kun pacificus en San Diego County; vagantaj individuoj de lagophonus kaj de la loĝantaro de la Roka Montaro, kiuj aspektas similaj al intergraduloj, ŝajne aperas en tiu teritorio. Loĝanta la tutan jaron.
Malgranda, sablokolora formo kun nedistinga striado, ĉefe sube. Ŝultra areo estas malhelbrunaj (kafokoloraj). Piedoj blankaj kaj kutime nemarkitaj.
  • B. v. mayensis (Nelson, 1901): Jukatana granda kornostrigo
Jukatano. Loĝanta la tutan jaron.
Malgranda kaj mezpala formo.
  • B. v. elachistus Brewster, 1902: Baskalifornia granda kornostrigo
Suda Baja California, Meksikio. Loĝanta la tutan jaron.
Simila laŭ koloro al pacificus, sed konsiderinde (5-10%) pli malgranda; tamen kelkaj koincidas.
  • B. v. heterocnemis (Oberholser, 1904): Nordorienta granda kornostrigo
Reproduktiĝas en orienta Kanado (Norda Kebekio, Labradoro, Novlando). Vintre, disigas suden al Ontario kaj nordokcidenta Usono. Dubinde distinga el saturatus (Holt et al. 1999).
Iom malhela kaj griza, tre striita formo. Palaj piedoj kun malhela punktaro.
  • B. v. lagophonus (Oberholser, 1904): Nordokcidenta granda kornostrigo
Reproduktiĝas el interna Alasko suden tra montaraj areoj de Brita Kolumbio al nordorienta Oregono, la Serpenta Rivero, kaj nordokcidenta Montano. Informoj pri vintro tiom sude kiom ĝis Koloradio kaj Teksaso. Dube distinga el saturatus (Holt et al. 1999).
Pli griza ol saturatus, sed similar entute. Piedoj kun malhela striado.
  • B. v. mesembrinus (Oberholser, 1904): Centramerika granda kornostrigo
Istmo de Tehuantepec al okcidenta Panamo. Loĝanta la tutan jaron.
Mezgranda formo; pli malhela ol mayensis.
  • B. v. ssp. nov.?: Rokamontara granda kornostrigo
La loĝantaro de la Roka Montaro povas konsistigi ne ankoraŭ priskribita subspecio. Ĝi reproduktiĝas sude de la Serpenta Rivero sude al Arizono, Novmeksikio, kaj la Montaro Guadalupe. Oriente, oni supozas, ke ĝi ĉeestas ĉe la ebenaĵo Modoc kaj la lago Mono. La nomo occidentalis povas esti uzata al tiuj birdoj depende de analizoj de la tipa specimeno; certe, ili estis inkluditaj en la supozata subspecio nomita tiele, sed intergradado inter pallescens kaj lagophonus kaj altituda migrado de birdoj de la Roka Montaro ne estis sufiĉe priserĉata ankoraŭ (Holt et al. 1999).
Mezgriza formo, intermeza inter lagophonus kaj pallescens. Meze striita kaj nuance sablokolora sube. Piedoj makulitaj.

La sinklera gufo de pleistoceno el Kalifornio, Bubo sinclairi, povus esti paleosubspecio de tiu ĉi specio (Howard 1947).

Referencoj en Media

  • La serio de libroj "Guardians of Ga'Hoole" havas du grandajn kornostrigojn kiel rolulojn, Bubo la Forĝisto kaj Skenĉo la Generalo Ablaho.
  • Rachel kaj Cassie de Animorphs ofte uzas formojn de grandaj kornostrigoj.

Media

Bildo

Video

Referencoj

  • Holt, Denver W., Berkley, Regan; Deppe, Caroline; Enríquez Rocha, Paula L.; Olsen, Penny D.; Petersen, Julie L.; Rangel Salazar, José Luis; Segars, Kelley P. & Wood, Kristin L. (1999): 69. Great Horned Owl. In: del Hoyo, J.; Elliott, A. & Sargatal, J. (eds): Handbook of Birds of the World, Volume 5: Barn-owls to Hummingbirds: 185, plate 10. Lynx Edicions, Barcelona. ISBN 84-87334-25-3
  • Howard, Hildegarde (1947): A preliminary survey of trends in avian evolution from Pleistocene to recent time. 'Condor 49(1): 10-13. PDF plena teksto

Vidu ankaŭ

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Granda kornostrigo: Brief Summary ( есперанто )

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La granda kornostrigo aŭ virginia kornostrigo, Bubo virginianus, estas specio de granda birdo el la ordo de strigoformaj, familio de strigedoj, kun granda plumtufo super ĉiu okulo. Ĝi estas indiĝena de Norda kaj Suda Ameriko. Ĝi estas adaptema birdo kun ampleksa teritorio, kvankam ne tiom disvastigata kiom tiu de la Turstrigo.

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Bubo virginianus ( шпански; кастиљски )

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El búho americano[2](Bubo virginianus), con los nombres locales en Brasil y Argentina derivados del guaraní: yacurú y jacurutú; también conocido en inglés como búho cornudo, búho tigre o búho real americano,[3]​ es una especie de ave de la familia Strigidae nativo de América. Es un ave extremadamente adaptable que vive en una gran extensión de territorio y es el búho más ampliamente distribuido en las Américas. Si bien es de gran tamaño, presenta gran variación (en tamaño y coloración) dentro de su rango de distribución (no consistente con la latitud). De todas las especies del género Bubo que hay en el mundo, el búho cornudo es el único que vive en América. Habita una gran variedad de hábitats, áreas abiertas asociadas a bosques y cuerpos de agua, bosques tropicales, templados, pantanosos y de coníferas, además manglares, desiertos y páramos, y asimismo vegetación secundaria y parques (este búho está asociado a paisajes fragmentados por ser tolerante a las actividades humanas). Está estrechamente relacionado con el Búho real que ocupa el mismo nicho ecológico en Eurasia. El busardo colirrojo podría considerarse su equivalente ecológico diurno pues comparte con el búho americano hábitats, presas y hábitos de anidación similares.

Taxonomía

El búho americano forma parte del género Bubo, que puede incluye otras especies de búho distribuidos predominantemente por Eurasia y África. Se cree que los antepasados de este búho llegaron a América a través del Puente de Beringia. Posteriormente, el Búho magallánico se separó del búho americano cuando este ya se encontraba ampliamente distribuido por América. Según el consenso general entre los científicos la división entre el búho nival y el búho americano se produjo en Eurasia y desde allí emigraron como especies separadas a América. Se ha sugerido que el búho americano y el búho real puedan ser conespecíficos, es decir, que ambos sean de la misma especie. Sin embargo, los estudios genéticos revelan que es el búho nival la especie viva más estrechamente relacionada con el búho americano. Se han encontrado restos fósiles del Pleistoceno de búhos pertenecientes al género Bubo en América del Norte pero parece ser que son especies diferentes o paleosubespecies del búho americano.

El número de subespecies es muy debatido entre los científicos. Generalmente, 12 subespecies son reconocidas:

Subespecies

Búho americano de Baja California (Bubo virginianus elachistus) De color similar al pacificus pero aún más oscuro y con más barras, parecido a un saturatus miniaturizado. Es considerablemente más pequeño que pacificus;se la considera la subespecie más pequeña.[4][5]​ Los machos tienen una longitud en el ala de 30 a 33 cm, una longitud de la cola de 17 a 20 cm y una longitud del pico de 3,3 a 3,8 cm. Vive en la misma zona todo el año y no realiza migraciones estacionales.

Búho americano nororiental (Bubo virginianus heterocnemis) Se reproduce en el este de Canadá (norte de Quebec, Labrador, Terranova). Su área de reproducción parece estar delineada al sur por el Río San Lorenzo. En invierno, esta raza puede dispersarse hacia el sur a lo largo de Ontario hasta el noreste de los Estados Unidos. Esta subespecie puede ser sinónimo de saturatus, aunque su distribución se aleja bastante de esta raza al este. B. v. heterocnemis está rodeado al oeste por la subespecie bastante más pálida subarcticus y al sur por virginianus, con esta última subespecie los rangos se superponen y pueden llegar a hibridar. Es una raza bastante oscura y gris, con una multitud de barras en el plumaje. Una forma bastante oscura y gris, fuertemente barrada. Algunos naturalistas defienden[¿quién?] que es la subespecie de mayor tamaño y los machos tienen un ala con una longitud de entre 35 y 36 cm y las hembras entre 37 y 39 cm.[6][7][8]​ En ambos sexos, la cola mide 22 a 25 cm y el pico es de 3,8 a 4,8 cm.

Búho americano de Alaska (Bubo virginianus lagophonus)

Búho americano del Yucatán (Bubo virginianus mayensis) Residente todo el año en la misma zona, sin realizar migraciones estacionales. Es una subespecie medianamente pálida, bastante similar a pallescens tanto en tono como en marcas ventrales. B. v. Mayensis es más pequeño que todas las subespescies de Norteamérica y es solo un poco más grande que elachistus. Los machos tienen unas alas con una longitud de 29-34 cm y una cola de 18-19 cm. Las hembras, en cambio, tienen unas alas de 30-35 cm de longitud y la cola entre 19-21 cm.

Búho americano centroamericano (Bubo virginianus mesembrinus)

Búho americano sudamericano o Ñacurutú (Bubo virginianus nacurutu) Incluye las subespecies propuestas scotinus, elutus y deserti. Es un ave pálida de color marrón en tonos tierra. Las aves del interior semiárido de Brasil, a menudo, son más blancas contra un fondo gris oscuro en las coberteras de la cola y los penachos en forma de orejas (a veces separadas como deserti). Esta especie es menos oscura que nigrescens. Es la única subespecie donde el iris es ámbar, no amarillo. B. v. nacurutu es una raza de tamaño mediano, más pequeña que la mayoría de América del Norte, pero no tan pequeña como algunas de las especies mexicanas. La longitud del ala es de 33–35 cm en los machos y 34-37 cm en las hembras. La cola en ambos sexos puede variar de 18 a 21 cm. La característica más notable de esta especie es su gran pico,[cita requerida] de 4,3 a 5,2 mm (1.7 a 2.0 pulgadas), que es el pico más grande en comparación con su tamaño total de entre todas las subespecies de búho americano.[7][9]

Búho americano andino (Bubo virginianus nigrescens) Es una subespecie oscura de color marrón grisáceo con marcadas manchas oscuras. Esta es la especie de color más oscuro, aunque compite por ello con saturatus y elachistus. Esta especie apenas tiene el matiz rojizo de otras subespecies, aunque algunos nigrescens pueden tener un disco facial de color canela. Es la subespecie más grande de Sudamérica, tiene una longitud de ala de 34–36 cm en machos y 35–38 cm en hembras. La cola en ambos sexos puede variar de 18 a 21 cm. La longitud del pico es de 4 a 5 cm, relativamente grande como sucede en nacurutu.

Búho americano de California (Bubo virginianus pacificus) Plumaje bastante marrón y con vermiculaciones menos marcadas que en saturatus pero más marcadas que en pallescens. Las garras están manchadas de oscuro. El disco facial a menudo tiene manchas oscuras. Esta raza de cuerpo bastante pequeño tiene el registro de menor peso en un macho del búho americano. La longitud del ala es de 30-36 cm en los machos y 33–37 cm en las hembras. La masa corporal varía de 680 a 1,272 g en los machos y de 825 a 1,668 g en las hembras. La longitud de la cola es de 17 a 21 cm y de 20 a 23 cm en machos y hembras, respectivamente.

Búho americano del desierto (Bubo virginianus pallescens) Es una subespecie de color beige oscuro con vermiculaciones en la parte inferior. Una raza pequeña, tiene una de longitud de ala ligeramente mayor que el pacificus, pero pesa menos de media. La longitud del ala es de 31–36 cm en los machos y 33–38 cm en las hembras. La masa corporal varía de 724 a 1.257 g en machos y de 801 a 1.550 g en hembras. En ambos sexos, la longitud de la cola es de 19 a 23 cm (7,5 a 9,3 pulgadas) y la longitud del pico es de 3,3 a 4,3 cm.

Búho americano del Pacífico (Bubo virginianus saturatus) Una subespecie oscura y pardusca en general con la parte inferior fuertemente barrada y moteada, con una base de color marrón oscuro. Las aves del interior (para algunos científicos separadas en lagophonus) tienden a tener una base más grisácea, siendo las lechuzas costeras puramente marrones. Por lo demás, los búhos del interior y de la costa son prácticamente iguales. El disco facial puede variar entre gris, gris rojizo y rojo oscuro. Las patas suelen ser de color gris oscuro y están más fuertemente barradas que en las otras subespecies norteamericanas. Es una subespecie bastante grande en líneas generales y los búhos de Alaska probablemente superen a todas las demás subespecies en tamaño con la excepción de heterocnemis. La longitud del ala es de 33–37 cm en los machos y 33–40 cm en las hembras. La longitud de la cola es de 19 a 24 cm y de 19 a 25 cm en machos y hembras respectivamente. En ambos sexos, la longitud del pico y tarso es de 3,5 a 4,4 cm.

Búho americano norteño (Bubo virginianus subarcticus) Esta es la subespecie más pálida de búho americano, con el color de fondo esencialmente blanquecino con un leve tono amarillo brillante en la parte superior; la nitidez de las vermiculaciones negras en la parte inferior es variable entre barras más definidas y otras más difusas. Esta raza muestra poca o ninguna coloración rojiza. Muestra una gran variación en su aspecto entre poblaciones siendo las de Estados Unidos de color grisáceo y bastante barrados y los de las zonas subárticas de Canadá que son de color muy pálido y apenas barrados. Las aves jóvenes muy pálidas son similares a las lechuzas nivales hembra y pueden ser identificadas erróneamente desde una distancia lejana. En el oeste de Canadá, subarcticus puede hibridar con saturatus y lo mismo sucede con heterocnemis en el este. En ambos casos, pueden producir híbridos de aspecto intermedio de tono rojizo, parecido a un virginianus pero con un contraste de colores más agudo. La longitud del ala es de 32–37 cm (12.7–14.6 in) en los machos y 33–39 cm en las hembras. La masa corporal varía de 865 a 1,460 g (1.907 a 3.219 lb) en los machos y de 1,112 a 2,046 g en las hembras. La longitud de la cola es de 20 a 22 cm y de 20 a 24 cm en machos y hembras, respectivamente. La longitud del pico es de 3,5 a 4,3 cm en ambos sexo.

Búho americano oriental (Bubo virginianus virginianus) La subespecie nominal es una forma de tono medio, ni muy oscura ni muy pálida. Tiende a tener un plumaje con bastante tonalidad rojiza y abundante barrado de color pardo oscuro en contraste con el color de fondo más claro. Los dedos suelen ser de color castaño, amarillento o crema y las patas están profusamente barradas. El disco facial es, por lo general, de un color rojo o anaranjado. Esta es una subespecie moderadamente grande, con una longitud del ala de 31–37 cm en machos y 34–38 cm en las hembras. mujeres. Esta es la subespecie conocida de mayor masa corporal, aunque esto podría cambiar oyes se desconoce los pesos de la mayoría de las subespecies, llegando los machos a pesar de 985 a 1,588 g y las hembras de 1,417 a 2,503 g. La longitud de la cola es de 19 a 23 cm (7.5 a 9.3 in) y la longitud del pico de 3,5 a 5 cm. B. v. virginianus es también la subespecie con los penachos más grandes en relación con su tamaño general.

Descripción

El búho americano es el búho más pesado existente en América Central y del Sur y es el segundo búho más pesado en América del Norte, después del búho nival con el que esta estrechamente relacionado. Tiene una constitución fuerte, con un cuerpo en forma de barril, una cabeza grande y alas anchas. Su tamaño puede variar considerablemente en su rango, con poblaciones en el interior de Alaska y Ontario siendo más grandes y poblaciones en California y Texas siendo más pequeñas, aunque las de la península de Yucatán y Baja California parecen ser aún más pequeñas. Los búhos adultos tienen una longitud de 43 a 64 cm, con un promedio de 55 cm y poseen una envergadura de 91 a 153 cm, con un promedio de 122 cm. Las hembras son algo más grandes que los machos. De media el peso corporal es de 1.608 g en las hembras y 1.224 g para los machos. Dependiendo de la subespecie, el peso máximo puede alcanzar 2,503 g.

La longitud del ala es de 29–40 cm, siendo unas alas relativamente pequeñas en comparación con la masa corporal del ave. La cola, que es relativamente corta, como es típico en la mayoría de los búhos, tiene una longitud de 17 a 25 cm. Al igual que otras especies de búhos, el búho americano es capaz de realizar un "vuelo silencioso", que es la forma en que los búhos vuelan sin hacer casi ningún ruido perceptible, a pesar de su gran tamaño. Esto es posible gracias a tres componentes de la estructura del ala del búho.

Las patas, los pies y las garras son grandes y poderosos. La longitud del pie completamente extendido, de una garra a otra, es de alrededor de 20 cm, en comparación con los 8 cm del búho chico, los 13 a 15 cm en las lechuza común y los 18 cm en el cárabo lapón. Los búhos americanos pueden aplicar una gran fuerza con sus garras, una presión considerablemente mayor que la que la mano humana es capaz de ejercer. En algunas hembras grandes, el poder de agarre del gran búho americano puede ser comparable a especies de rapaces mucho más grandes como el águila real. El pico duro e inflexible del búho americano mide 3.3–5.2 cm de largo.

Las aberturas externas del oído, que están ocultas por plumas en los costados de la cabeza, son relativamente pequeñas, con el oído izquierdo ligeramente más grande que el derecho. Al igual que otras especies nocturnas, el búho americano tiene los oídos asimétricos lo que le permite la triangulación de los sonidos al cazar en la oscuridad. Los oídos a diferentes alturas, aunque la diferencia no sea muy grande, se diferencian lo suficiente como para que el búho pueda usar el tiempo y la dirección de las ondas de sonido que golpean cada oído para ubicar con precisión la presa. La forma de disco de sus caras también ayuda a dirigir los sonidos que escuchan hacia sus oídos. Si bien se desconoce la verdadera naturaleza o propósito de los penachos emplumados con forma de orejas que están presentes en el búho americano, los investigadores coinciden en que los mismos no juegan ningún papel en la capacidad auditiva del búho. Se estima que su audición es hasta diez veces mayor que la de un ser humano.

Los ojos del búho americano, un poco más pequeños que los ojos de un ser humano, son grandes incluso para un búho y se encuentran entre los ojos más grandes de todos los vertebrados terrestres proporcionalmente al tamaño general del cuerpo. El búho americano tiene ojos cilíndricos que crean una mayor distancia desde la lente del ojo hasta la retina, lo que le permite actuar más como un teleobjetivo para una mejor visión a mayor distancia que la que le proporcionaría unos ojos redondos. Sus ojos están visualmente muy adaptados para la caza nocturna y proporcionan un campo de visión amplio, casi completamente binocular. En lugar de girar los ojos, el búho debe girar toda su cabeza, y puede girar su cuello 270 °. El iris es amarillo, excepto en el búho americano sudamericano que son de color ámbar (B. v. nacurutu).

La finalidad principal del plumaje del búho americano es el camuflaje. Las partes inferiores del cuerpo son generalmente claras con vermiculaciones pardas; las partes dorsales y la parte superior de las alas son moteados de diversos tonos de marrón. Todas las subespecies también tienen vermiculaciones, en distinta intensidad, en los lados.

Posee una mancha blanca de tamaño variable en la garganta. Esta mancha puede extenderse hasta la mitad del pecho e, incluso en ejemplares particularmente pálidos, puede agrandarse hasta el vientre. Los búhos americanos de Sudamérica suelen tener esta mancha blanca más pequeña y rara vez se extiende hasta el pecho. Existen variaciones en la coloración del plumaje tanto individuales como regionales, con los búhos del subártico siendo de color claro y tonos pálidos, mientras que los de la costa del Pacífico de Norteamérica, los de América Central y gran parte de Sudamérica suelen tener un color marrón oscuro parcheado con manchas negruzcas. La piel de los pies y las patas, aunque casi completamente oculta tras las plumas, es negra. El pico y las garras es de color gris oscuro.

Todos los búhos americanos tienen un disco facial. Este puede ser de color rojizo, marrón o gris (variando según la zona geográfica y la subespecie) y está demarcado por un borde oscuro. Las "orejas" de esta especie son en realidad penachos de plumas. El propósito de los mismos no se ha identificado completamente, pero está generalmente aceptada la teoría de que sirven como una señal visual en las interacciones territoriales y sociosexuales con otros búhos.

Distribución y hábitat

El búho americano se distribuye por todo América del Norte con la excepción de las zonas más frías del ártico donde es sustituido por el búho nival. En América Central su distribución está más fragmentada y solo se encuentra en enclaves aislados. En América del Sur se distribuye por el norte del subcontinente desde Colombia hasta las Guayanas y el noreste de Brasil y también en las cordilleras andinas de Ecuador y Perú. En el sur de Sudamérica también ocupa una amplia zona entre Bolivia y el sureste Brasil hasta el norte de Argentina; más al sur es sustituido por el búho magallánico. La especie esta ausente de lo más profundo de los bosques tropicales del Amazonas, así como de islas del Caribe. Es la segunda especie de búho con una mayor distribución en las Américas tras la Lechuza común.

Esta especie de búho se encuentra entre las especies de aves más adaptables del mundo en lo que se refiere a su hábitat. Puede vivir en árboles pertenecientes a todo tipo de hábitats: bosques templados, bosques de coníferas, bosques mixtos, bosques tropicales, pampas, praderas, zonas montañosas, desiertos, tundra, costas rocosas, manglares e incluso algunas áreas urbanas. Se encuentra ausente de las áreas con climas más extremos como el interior de los desiertos de Mojave y Sonora. También evita las zonas de bosque profundo y prefiere vivir en áreas de bosque más fragmentado con zonas abiertas donde cazar y grupos de árboles donde descansar y refugiarse. En lugares abiertos como praderas y desiertos pueden residir todo el año mientras existan cañones rocosos, barrancos o zonas arboladas que les sirvan de refugio y lugar de anidación.

En las zonas montañosas de América del Norte, generalmente están ausentes por encima del límite del bosque, pero se pueden encontrar de hasta 2,100 m en California y 3,300 m en las Montañas Rocosas. En las montañas de los Andes, por otro lado, se han adaptado a ser verdaderas aves montanas, a menudo se encuentran al menos a 3,300 msnm y se registran regularmente en zonas de pastizales de la Puna sin árboles a 4,100 a 4,500 m en Ecuador y Perú. En general, es raro verlos en humedales. Aunque se adapta bien a la vida en áreas urbanas prefiere zonas con menor actividad humana como grandes parques y zonas de cultivo. Todos los búhos americanos son aves residentes que no realizan migraciones salvo cuando las aves no emparejadas o ejemplares jóvenes se mueven en busca de pareja o territorio.

Comportamiento

Anida en oquedades de troncos, y puede poner de dos a tres huevos. Se alimenta de pequeños mamíferos, reptiles e incluso peces. Se ha reproducido en cautiverio. Se utilizó y se sigue utilizando para cetrería.

Conservación

Aunque la especie presenta aparentemente amplia distribución en México, existe poca información sobre el estado actual de sus poblaciones y rango de distribución. Al parecer, va desde el norte del país, incluyendo Baja California Norte y Sur, hasta el sur de México incluyendo la Península de Yucatán. La IUCN2019-1 considera a la especie como de preocupación menor. Los principales riesgos que amenazan a la especie son la pérdida del hábitat, disminución de presas, cacería ilegal, uso de plaguicidas y colisión con automóviles, cables eléctricos y construcciones.[10]

Referencias

  1. BirdLife International (2014). «Bubo virginianus». Lista Roja de especies amenazadas de la UICN 2015.2 (en inglés). ISSN 2307-8235. Consultado el 26 de agosto de 2015.
  2. Bernis, F; De Juana, E; Del Hoyo, J; Fernández-Cruz, M; Ferrer, X; Sáez-Royuela, R; Sargatal, J (2000). «Nombres en castellano de las aves del mundo recomendados por la Sociedad Española de Ornitología (Quinta parte: Strigiformes, Caprimulgiformes y Apodiformes)». Ardeola. Handbook of the Birds of the World (Madrid: SEO/BirdLife) 47 (1): 123-130. ISSN 0570-7358. Consultado el 30 de octubre de 2011.
  3. «Instituto Nacional de Ecología». Archivado desde el original el 18 de octubre de 2008.
  4. König, Claus; Weick, Friedhelm (2008). Christopher Helm, ed. Owls of the World (2nd ed.). ISBN 9781408108840.
  5. Webster, J. D. and R. T. Orr. (1958). Variation in the Great Horned Owls of Middle America. p. 134-142.
  6. Voous, K.H. (1988). Owls of the Northern Hemisphere. The MIT Press. ISBN 0262220350.
  7. a b Houston, C. Stuart, Dwight G. Smith and Christoph Rohner (1998). Great Horned Owl (Bubo virginianus), The Birds of North America Online. Ithaca: Cornell Lab of Ornithology; Retrieved from the Birds of North America Online.
  8. Taverner, P. A. (1942). Canadian Races of the Great Horned Owls. The Auk. p. 234-245.
  9. Mikkola, H (2012). Owls of the World: A Photographic Guide. Firefly Books. ISBN 9781770851368.
  10. «Enciclovida (consultado el 20 de enero del 2020).».

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Bubo virginianus: Brief Summary ( шпански; кастиљски )

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El búho americano​ (Bubo virginianus), con los nombres locales en Brasil y Argentina derivados del guaraní: yacurú y jacurutú; también conocido en inglés como búho cornudo, búho tigre o búho real americano,​ es una especie de ave de la familia Strigidae nativo de América. Es un ave extremadamente adaptable que vive en una gran extensión de territorio y es el búho más ampliamente distribuido en las Américas. Si bien es de gran tamaño, presenta gran variación (en tamaño y coloración) dentro de su rango de distribución (no consistente con la latitud). De todas las especies del género Bubo que hay en el mundo, el búho cornudo es el único que vive en América. Habita una gran variedad de hábitats, áreas abiertas asociadas a bosques y cuerpos de agua, bosques tropicales, templados, pantanosos y de coníferas, además manglares, desiertos y páramos, y asimismo vegetación secundaria y parques (este búho está asociado a paisajes fragmentados por ser tolerante a las actividades humanas). Está estrechamente relacionado con el Búho real que ocupa el mismo nicho ecológico en Eurasia. El busardo colirrojo podría considerarse su equivalente ecológico diurno pues comparte con el búho americano hábitats, presas y hábitos de anidación similares.

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Bubo virginianus ( баскиски )

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Bubo virginianus Bubo generoko animalia da. Hegaztien barruko Strigidae familian sailkatua dago.

Erreferentziak

  1. (Ingelesez)BirdLife International (2012) Species factsheet. www.birdlife.org webgunetitik jaitsia 2012/05/07an
  2. (Ingelesez) IOC Master List

Ikus, gainera

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Bubo virginianus: Brief Summary ( баскиски )

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Bubo virginianus Bubo generoko animalia da. Hegaztien barruko Strigidae familian sailkatua dago.

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Amerikanhuuhkaja ( фински )

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Amerikanhuuhkaja (Bubo virginianus) on amerikkalainen suurikokoinen pöllö.

Koko ja ulkonäkö

Linnun pituus on 46–63,5 cm, siipien kärkiväli 91–152 cm ja paino 900–1 800 g. Kooltaan amerikanhuuhkaja on selvästi huuhkajaa pienempi. Sen väritys vaihtelee punaruskeasta harmaaseen ja mustavalkoiseen. Sillä on keltaiset silmät oranssin naamakiehkuran keskellä ja pitkät korvatöyhdöt. Naaras on koirasta kookkaampi.

Esiintyminen

Amerikanhuuhkaja elää kaikissa kolmessa Uuden maailman maanosassa, pohjoisessa Alaskasta ja Kanadan keskiosista Yhdysvaltain kautta Keski-Amerikkaan ja monin paikoin Etelä-Amerikassa, kuten Andeilla, Amazonin altaan eteläpuolella ja aivan mantereen koillisella rannikkokaistaleella. Sen elinympäristön ala on noin 24 miljoonaa neliökilometriä ja maailman populaation koko on noin 5,3 miljoonaa yksilöä. Se on enimmäkseen paikkalintu, jonka pohjoisimmat kannat voivat muuttaa hieman etelämmäksi talveksi.

Elinympäristö

Lajille kelpaavat monenlaiset elinympäristöt tiheistä metsistä aavikoihin ja kaupunkien puistoihin.

Lisääntyminen

Amerikanhuuhkaja ei rakenna varsinaista pesää, vaan pesii esimerkiksi muiden lintujen, kuten varislintujen, haukkojen tai haikaroiden vanhoihin pesii, rakennuksiin, kalliojyrkänteen ulkonemalle, puun onkaloon tai vanhaan oravanpesään. Naaras munii 2–4 munaa, joita se hautoo 26–35 päivää. Poikaset lähtevät pesästä 6–7 viikon ikäisinä ja oppivat lentämään 9–10 viikkoisina, jonka jälkeen emot ruokkivat niitä vielä joidenkin viikkojen ajan. Poikaset itsenäistyvät syksyllä ja lähtevät vaeltamaan jopa 250 kilometrin päähän. Laji on yksiavioinen ja sen reviirin koko on noin 2,5 neliökilometriä. Vankeudessa se on elänyt yli 30-vuotiaaksi, luonnossa vanhin yksilö on ollut 13-vuotias.

Ravinto

Amerikanhuuhkajan pääravintoa ovat kanit ja jänikset, mutta sen ruokavalioon kuuluvat myös jyrsijät ja muut nisäkkäät, linnut, matelijat, sammakkoeläimet, kalat, kovakuoriaiset ynnä muut selkärangattomat ja tuoreet raadot.

Lähteet

  1. BirdLife International: Bubo virginianus IUCN Red List of Threatened Species. Version 2014.3. 2014. International Union for Conservation of Nature, IUCN, Iucnredlist.org. Viitattu 20.2.2015. (englanniksi)
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Amerikanhuuhkaja: Brief Summary ( фински )

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Amerikanhuuhkaja (Bubo virginianus) on amerikkalainen suurikokoinen pöllö.

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Grand-duc d'Amérique ( француски )

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Bubo virginianus

Le Grand-duc d'Amérique[a] ou Grand-duc de Virginie (Bubo virginianus) est une espèce de rapaces nocturnes appartenant à la famille des Strigidae et à la sous-famille des Striginae. Il est souvent comparé avec son cousin le Grand-duc d'Europe avec qui il partage de nombreux points communs.

Généralités et description

Cet oiseau aux aigrettes caractéristiques est le deuxième plus grand des hiboux d'Amérique après le Harfang des neiges; sa taille varie cependant significativement selon son habitat et l'abondance de la nourriture[4].

Avec un bec crochu, de grandes ailes, des serres puissantes, le Grand-duc est parfaitement adapté à la chasse nocturne d'animaux de petite taille. Ses yeux jaunes perçants et ses aigrettes en font un oiseau impressionnant pour l'homme.

Cet oiseau mesure 45 à 63 cm de longueur pour une envergure de 90 à 162 cm et une masse de 675 g à 2,5 kg. Il ne présente pas de dimorphisme sexuel en termes de couleurs, mais en termes de grosseur, les femelles étant un tiers plus grosse que les mâles comme chez la plupart des oiseaux de proies.

Il a la gorge blanche.

Répartition et habitat

 src=
Répartition

Le Grand-duc d'Amérique niche dans la majeure partie du continent américain. Son aire de répartition s'étend loin au nord, occupant une bonne partie du Canada, et en Amérique du Sud jusqu'au nord de l'Argentine, ainsi qu'au Brésil et en Bolivie.[5]

 src=
Ses yeux jaunes et ses aigrettes.

Cet oiseau est un des hiboux les plus adaptables, résidant dans les arbres de tout type de forêts, de jungles, de prairies, de déserts, de toundras, de mangroves et même de zones urbaines. Il évite cependant les zones trop extrêmes, comme le cœur des déserts, ou trop boisées. On le retrouve rarement en altitude en Amérique du Nord[6], alors qu'il s'est bien adapté aux plateaux des Andes dans le sud de son aire de répartition.[7]

Éthologie et reproduction

Généralement sédentaire, cet oiseau défend son territoire, surtout en période de reproduction, avec toutefois des jeunes ayant un comportement non territorial[8].
Vocalisations : Très bruyant à la saison de reproduction, il émet un hululement puissant[9], typique du chant des hiboux[10].
Il niche dans d'anciens nids d'autres grands oiseaux, dans des trous d'arbres, des corniches de falaise et même au sol.

Habituellement le plus actif au crépuscule et à l'aube, c'est un chasseur efficace. Il bénéficie d'une bonne vision nocturne et d'une bonne acuité visuelle[11] ainsi que d'une ouïe particulièrement développée.

Alimentation

Il capture surtout de petits mammifères (campagnols, etc.) dont certains ont développé des "comportements anti-prédateurs"[12], des insectes, des reptiles, des amphibiens et des oiseaux (y compris d'autres rapaces nocturnes et des gélinottes).

Il peut chasser et manger les moufettes, grâce à son odorat très peu développé. La prédation a été observée sur tous les types de mouffettes nord américaines, dans certains cas sur des animaux au moins trois fois plus gros que le Grand-duc prédateur [13],[14],[15], et un nid a été trouvé contenant les restes de 57 mouffettes de tous types [16]. Une conséquence est que les nids de Grands-ducs ont tendance à manifester une forte odeur de mouffette[17],[18].

Déplacements et migrations

Cet oiseau est sédentaire. Après leur émancipation, les jeunes explorent leur environnement pour trouver un territoire disponible et leur convenant et s'y établir.

Menaces

L'espèce est en régression, probablement à cause de la destruction, fragmentation et régression de ses habitats, et à cause d'une dégradation de la qualité de certaines de ses proies, contaminées par des pesticides, métaux lourds (plomb notamment, qui est cause de saturnisme aviaire[19]. Des parasitoses ou attaques des jeunes au nid par des tiques ou mouches hématophages peuvent affaiblir les jeunes et faciliter certaines maladies (leucocytozoonoses)[20].

Galerie

Notes et références

Notes

  1. Cette appellation est normalisée dans plusieurs langues dont le français par le Comité ornithologique international[1]. Cette orthographe diffère de celle des dictionnaires français Robert, Larousse[2] et Académie française[3] qui écrivent « grand duc », « moyen duc », « petit duc » sans trait d’union.

Références

  1. « Listes multilingues des noms d’oiseaux, selon plusieurs formats », sur worldbirdnames.org, Comité ornithologique international (consulté le 18 septembre 2018) dont cette version Excel 8.2.
  2. « Larousse en ligne : entrée « duc » », sur larousse.fr (consulté le 19 septembre 2018).
  3. « Dictionnaire de l’Académie française, 9e édition : entrée « Duc », sens II », sur academie.atilf.fr (consulté le 19 septembre 2018).
  4. McGillivray, B. (1989), Geographic variation in size and reserve size dimorphism of the great horned owl in North America. The Condor, 91: 777-786.
  5. Claus König, Owls of the World., A & C Black, 2009 (ISBN 978-1-4081-0884-0 et 1-4081-0884-4, OCLC , lire en ligne)
  6. Ad Cameron, Owls of the Northern Hemisphere, MIT Press, 1989 (ISBN 0-262-22035-0 et 978-0-262-22035-4, OCLC , lire en ligne)
  7. Joseph Ewan, Jon Fjeldsa et Niels Krabbe, « Birds of the High Andes: A Manual to the Birds of the Temperate Zone of the Andes and Patagonia, South America », Taxon, vol. 40, no 4,‎ novembre 1991, p. 700 (ISSN , DOI , lire en ligne, consulté le 13 mars 2022)
  8. Rohner, C. (2001), Non-territorial floaters in great horned owls (Bubo virginianus). 2d Owl Symposium: 347-362. allo (résumé)
  9. Kinstler, K. (2009) Great horned owl Bubo virginianus vocalizations and associated behaviours. Ardea, 97/4: 413-420
  10. Miller, A. (1934), The vocal apparatus of some North American owls. The Condor, 36/5: 204-213
  11. Fite, K. (1973), Anatomical and behavioral correlates of visual acuity in the great horned owl. Vision Research, 13/2: 219-230
  12. Rohner, C., C. Krebs. (1996) Owl predation on snowshoe hares: Consequences of Antipredator Behaviour. Oecologia, 108/2: 303-310
  13. Bent, A. C. 1938. Life histories of North American birds of prey, Part 2. U.S. National Museum Bulletin 170:295-357.
  14. Cromrich, L. A., Holt, D. W., & Leasure, S. M. (2002). Trophic niche of North American great horned owls. Journal of Raptor Research, 36(1), 58-65.
  15. Huey, L. M. (1931). Skunks as Prey for Owls. The Wilson Bulletin, 224-224
  16. Luke Hunter, Carnivores of the World, Princeton, NJ, Princeton University Press, 2011 (ISBN 978-0-691-15228-8)
  17. Houston, C. Stuart, Dwight G. Smith and Christoph Rohner. 1998. Great Horned Owl (Bubo virginianus), The Birds of North America Online (A. Poole, Ed.)
  18. Crocoll, S. T. (1984). Breeding biology of broad-winged and red-shouldered hawks in western New York (Doctoral dissertation, State University of New York at Fredonia, 1984--Department of Biology.)
  19. Weir, D., Hanson, A. (1989), Food habits of great horned owls (Bubo virginianus) in the Northern Taiga of the Yukon Territory and Alaska. Can. Field Nat. 103, 12–17 résumé
  20. Hunter, D., C. Rohner, D. Currie. (1997), Mortality in fledgling great horned owls from black fly hematophaga and leucocytozoonosis. Journal of Wildlife Diseases, 33/3: 486-491

Voir aussi

Références taxonomiques

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Grand-duc d'Amérique: Brief Summary ( француски )

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Bubo virginianus

Le Grand-duc d'Amérique ou Grand-duc de Virginie (Bubo virginianus) est une espèce de rapaces nocturnes appartenant à la famille des Strigidae et à la sous-famille des Striginae. Il est souvent comparé avec son cousin le Grand-duc d'Europe avec qui il partage de nombreux points communs.

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Mórulchabhán cluasach ( ирски )

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Is éan é an Mórulchabhán cluasach Is baill d'fhine na Strigidae iad.


Ainmhí
Is síol ainmhí é an t-alt seo. Cuir leis, chun cuidiú leis an Vicipéid.
Má tá alt níos forbartha le fáil i dteanga eile, is féidir leat aistriúchán Gaeilge a dhéanamh.


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Bufo americano ( галициски )

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O bufo americano (Bubo virginianus) é unha especie de ave estrixiforme da familia dos bufos (Strigidae). É nocturna, de plumaxe raiada.

Subespecies

  • B. v. virginianus (Gmelin, 1788)
  • B. v. nacurutu, (Vieillot, 1817): ñacurutú
  • B. v. subarcticus Hoy, 1852
  • B. v. pacificus Cassin, 1854
  • B. v. saturatus Ridgway, 1877
  • B. v. nigrescens Berlepsch, 1884
  • B. v. pallescens Stone, 1897
  • B. v. mayensis (Nelson, 1901)
  • B. v. elachistus Brewster, 1902.
  • B. v. heterocnemis (Oberholser, 1904)
  • B. v. lagophonus (Oberholser, 1904).
  • B. v. magellanicus
  • B. v. mesembrinus (Oberholser, 1904)

Notas

  1. BirdLife International (2014). "Bubo virginianus". Lista Vermella da IUCN (IUCN) 2014: e.T61752071A61752159. Consultado o 14 de febreiro de 2016.

Véxase tamén

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Bufo americano: Brief Summary ( галициски )

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O bufo americano (Bubo virginianus) é unha especie de ave estrixiforme da familia dos bufos (Strigidae). É nocturna, de plumaxe raiada.

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Bubo virginianus ( италијански )

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Il gufo della Virginia (Bubo virginianus Gmelin, 1788) è un grande rapace notturno della famiglia degli Strigidi.[2]

Descrizione

Misura da 50 a 66 cm, pesa dai 675 ai 2500 grammi e ha un'apertura alare di 140–170 cm. È il gufo più grande del continente americano. Ha una corporatura molto robusta con piedi grandi e artigli affilati. Il piumaggio è vario, ma sempre di tonalità brune tranne sulla gola che è sempre bianca. Si va dal marroncino chiaro, quasi biancastro, delle sottospecie che vivono più a nord, al bruno scuro di quelle che vivono nelle foreste. In tutti i casi comunque il piumaggio è striato di nero dal capo alla coda. Il becco è adunco, gli occhi giallo chiaro, ma il tratto distintivo di questo gufo sono i grandi ciuffi di piume sulle orecchie.

Distribuzione e habitat

Vive in tutto il continente americano dal Canada fino al Cile e all'Argentina (è stato avvistato anche vicino allo Stretto di Magellano e più a sud sulle isole della Georgia del Sud e sulle Sandwich Australi), con l'esclusione delle zone polari, del fitto della foresta amazzonica e di alcune isole dei Caraibi.
Il largo areale permette al gufo della Virginia di frequentare posti assai diversi tra loro. Principalmente lo si incontra nei fitti boschi di conifere o di latifoglie, ma è presente anche lungo burroni e canyon rocciosi, nel deserto e nella taiga canadese, ad altezze variabili ma anche in alta montagna.

Biologia

 src=
Gufi della Virginia in volo

È un rapace stanziale e solitario, fortemente territoriale. Difende assiduamente i propri territori di caccia e di nidificazione, non esitando ad attaccare qualsiasi intruso, compreso l'uomo. Sebbene veda anche di giorno, diviene attivo soprattutto la notte sia perché la vista è migliore, sia perché le prede del gufo sono animali notturni. Il volo è silenzioso, grazie alle soffici piume, ed inoltre è dotato di un udito eccellente. Al contrario, l'olfatto è estremamente limitato, quasi assente, il che lo rende capace di cacciare le moffette senza temere le secrezioni dall'odore nauseabondo che usano come difesa. I piccoli se si sentono minacciati gonfiano il piumaggio per sembrare più grandi e minacciosi.

Alimentazione

Il gufo della Virginia, come gli altri gufi, è un carnivoro. Si nutre solitamente di piccoli mammiferi come conigli, topi, scoiattoli, marmotte, moffette e ratti. Mangia anche altri uccelli di piccole e grandi dimensioni come quaglie e anatre, o oche e tacchini, e talvolta persino altri gufi. Non disdegna rane e altri anfibi, rettili e raramente anche insetti. Le parti non digeribili delle prede, come ossa e piume, vengono rigettate sotto forma di borre.

Riproduzione

 src=
Tre piccoli nel nido

Il periodo riproduttivo del gufo della Virginia inizia tra gennaio e i primi di febbraio. Maschi e femmine diventano molto loquaci, modulando una certa quantità di note per attrarre il partner. Una volta accoppiati, la femmina depone da una a cinque (in genere due o tre) uova nella cavità di un albero o nei nidi abbandonati di altri uccelli. Il periodo di incubazione delle uova è di circa 30 giorni, dopodiché i genitori accudiranno i piccoli per oltre un mese dopo l'impiumazione che avviene ai due mesi dalla schiusa.

Sistematica

Esistono 14 sottospecie di Bubo virginianus:[2]

  • B. v. algistus (Oberholser, 1904)
  • B. v. lagophonus (Oberholser, 1904)
  • B. v. saturatus Ridgway, 1877
  • B. v. pacificus Cassin, 1854
  • B. v. subarcticus Hoy, 1853
  • B. v. pallescens Stone, 1897
  • B. v. pinorum Dickerman & Johnson, AB, 2008
  • B. v. heterocnemis (Oberholser, 1904)
  • B. v. virginianus (Gmelin, JF, 1788)
  • B. v. elachistus Brewster, 1902
  • B. v. mayensis Nelson, 1901
  • B. v. mesembrinus (Oberholser, 1904)
  • B. v. nigrescens Berlepsch, 1884
  • B. v. nacurutu (Vieillot, 1817)

Note

  1. ^ (EN) BirdLife International 2012, Bubo virginianus, su IUCN Red List of Threatened Species, Versione 2020.2, IUCN, 2020.
  2. ^ a b (EN) Gill F. and Donsker D. (eds), Family Strigidae, in IOC World Bird Names (ver 9.2), International Ornithologists’ Union, 2019. URL consultato il 13 maggio 2014.

Bibliografia

  • AA. VV, Grande enciclopedia per ragazzi, Animali, Vol. 2 Uccelli e Mammiferi, Edizione Speciale per la Repubblica su licenza Mondadori, 2005, p. 91, SBN ITICCUIEI496892.

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Bubo virginianus: Brief Summary ( италијански )

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Il gufo della Virginia (Bubo virginianus Gmelin, 1788) è un grande rapace notturno della famiglia degli Strigidi.

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Amerikaanse oehoe ( холандски; фламански )

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Vogels

De Amerikaanse oehoe (Bubo virginianus) is een algemene uilensoort van het Amerikaanse continent.

Kenmerken

Met een grootte van 43-55 cm is de oehoe één van de grootste uilensoorten, maar een slag kleiner dan de Europese oehoe. Het dier heeft duidelijk horizontale oorpluimen. Het verenkleed is bruin.

Leefwijze

's Nachts gaat deze soort op jacht naar kleine zoogdieren, vogels, reptielen en ongewervelde dieren. De grootte van de prooi varieert van grote insecten tot skunks, konijnen en ruigpoothoenders. De oehoe gebruikt vaak verlaten nesten van buizerds als nest. Daarnaast nestelt hij ook in grote boomholten of menselijke bouwsels.

Verspreiding en leefgebied

Deze vogel is in een groot aantal biotopen te vinden: laagland- en bergbossen, savannes, bouwland en zelfs voorsteden.

De soort telt 14 ondersoorten:

  • B. v. algistus: westelijk Alaska.
  • B. v. lagophonus: van centraal Alaska tot noordoostelijk Oregon, Idaho en noordwestelijk Montana.
  • B. v. saturatus: van de zuidoostkust van Alaska tot de noordkust van Californië.
  • B. v. pacificus: van de kust van centraal Californië tot noordwestelijk Baja California.
  • B. v. subarcticus: van het westelijke deel van Centraal-Canada tot noordelijk Idaho.
  • B. v. pallescens: van de zuidwestelijke Verenigde Staten tot zuidelijk Mexico.
  • B. v. pinorum: van zuidelijk Idaho tot noordelijk Arizona en noordelijk New Mexico.
  • B. v. heterocnemis: van noordoostelijk Canada tot het gebied van de Grote Meren.
  • B. v. virginianus: van zuidoostelijk Canada tot de centrale en oostelijke Verenigde Staten.
  • B. v. elachistus: zuidelijk Baja California.
  • B. v. mayensis: Yucatán.
  • B. v. mesembrinus: van zuidelijk Mexico tot westelijk Panama.
  • B. v. nigrescens: van Colombia tot noordwestelijk Peru.
  • B. v. nacurutu: van oostelijk Colombia via de Guyana's tot noordoostelijk Brazilië, Argentinië, Bolivia en centraal Peru.

Externe links

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Amerikaanse oehoe: Brief Summary ( холандски; фламански )

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De Amerikaanse oehoe (Bubo virginianus) is een algemene uilensoort van het Amerikaanse continent.

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Amerikahubro ( норвешки )

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Amerikahubro (Bubo virginianus) er en ugle i gruppen Bubo. Den hører hjemme i både Nord- og Sør-Amerika, men er ikke fullt så vanlig som tårnuglen. Amerikahubro er aldri blitt observert i palearktis. Den er provinsfugl for den canadiske provinsen Alberta. Amerikahubro kan lett forveksles med Bubo magellanicus, som man en tid trodde tilhørte denne arten.

Beskrivelse

Amerikahubro måler fra 46 til 68 cm og har et vingespenn på 101 til 152 cm. En gjennomsnittlig størrelse er 55 cm med et vingespenn på 124 cm og vekt på 1400 gram. Hunnen er større enn hannen, og de største individene finnes i de nordligste regionene. Mot ekvator er de gjerne mindre.

Voksne fugler har store øredusker, rødlig, brunt eller grått ansikt og en hvit flekk på halsen. Iris er gul, unntatt for arten B. v. nacurutu, som har en amber farge på iris. Øreduskene er ikke ører, men fjærdusker. Legger og føtter er dekket av fjær. Undersiden av fuglen er lys med brune kanter. Det er både individuelle og regionale variasjoner i fargene; fugler fra nord har en lysebrun farge mens fugler fra Sentral-Amerika kan være mørk sjokoladebrune.

 src=
Amerikahubro har store øyne

Amerikahubroen har et ekstremt godt syn i lite lys, noe som er nødvendig for å se byttet også i mørke. Fordi den ikke kan bevege øynene, kan den vri halsen i 270 grader for å se i andre retninger uten å flytte hele kroppen. Øynene er nesten like store som menneskeøyne og ligger fast i øyehulen.

Også hørselen er svært god. Hørselen oppfatter dybde bedre enn mennesket og fanger også opp høydeforskjell. Fordi ugleører ikke ligger likt på hver side av hodet, det høyre øret er litt høyere enn det venstre og har en litt annen vinkel i plasseringen, kan en ugle som snur og bikker på hodet, fastlegge både horisontal og vertikal retning av lyd. Ettersom de hører i stereo, kan de plassere byttet nøyaktig ut fra lyden.

Habitat og utbredelse

Amerikahubro finnes nesten over hele Nord- og Sør-Amerika. De finnes i de fleste omgivelser, men er ikke så vanlige i de mest ekstreme områdene (tundra, sentrale ørkenområder og tykke regnskoger). Men den finnes i blandingsskog, tropisk regnskog, pampas, prærie, fjellområder, klippekyst og mangrovesumper, til og med i byområder.

Levevis

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Amerikahubro med hare
Malt av Louis Agassiz Fuertes (artist, 1874-1927)

Fuglene jakter om natten ved å vente på et utsiktspunkt og kaste seg ned på byttet, som kan variere mye, men for det meste er små til middels store pattedyr som rotter, ekorn, mus, vånd, murmeldyr, skunker, spissmus, flaggermus, vaskebjørner, katter og til og med trepinnsvin. Harer og bomullshalekaniner kan også etes, så vel som fugler av ulike slag fra fuglekonge til hegre. Dette inkluderer sothøner og ender, men også rovfugler som snøugler og fiskeørn kan være på menyen sammen med krypdyr, amfibier, fisk, krepsdyr og insekter. I nord, hvor større bytte ikke spises opp med det samme kan den la maten fryse og siden tine den opp igjen med sin egen kroppsvarme.

Det blir ofte sagt at amerikahubro er den farligste uglen, og det er rapportert at den har drept mennesker. Det bør i den forbindelse nevnes at slike angrep ikke er for mat og at det eneste kjente dødelige angrepet ble forårsaket av offeret selv, da han prøvde å stjele egg eller kyllinger fra reiret til hubroen.

Reir og unger

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Unger av amerikahubro i reiret

Amerikahubro er en av de fugler som tidligst får unger i Nord-Amerika. Man hører fuglene kalle fra oktober, og i desember har de valgt make. Da kan man høre dem i duett. Kallingen er en dyp, men høylytt «ho-ho-hoo hoo hoo». Noen ganger er det bare fire stavelser i stedet for fem. Hunnens ligger høyere enn hannens og stiger i tone mot slutten. Ungfuglenes hissing og skrikende lyder blir ofte tatt for å komme fra tårnugler.

Så legges eggene i januar eller tidlig i februar. For fugler i mer tropisk klima er sesongen mer ubestemmelig.

Amerikahubro tar ofte over reir etter andre større fugler, noen ganger legger de fjær til i reiret, men til vanlig ikke mye mer. De kan velge seg gamle reir etter kråke, ravn, hauk eller store ekornreir. Men de er ikke avhengige av gamle reir og kan bruke huler i trær, stein, fraflyttede bygninger eller kunstige plattformer.

Vanligvis er det to egg i hvert kull, men det er variasjoner mellom ett og fem. Gjennomsnittsegget er 46,5 mm bredt og 55,2 mm langt. Vekta ligger omkring 50 gram. Rugeperioden strekker seg fra 30 til 37 dager, i snitt 33 dager. Så følger en periode på to uker med kontinuerlig foring, siden reduseres matingen. Etter seks uker flytter unge ugler ut på greiner i nærheten, en uke seinere begynner de å fly. Men man har sett at de tigger foreldrene om mat sent i oktober, fem måneder etter at de forlot reiret. De forlater ikke foreldrene før like før disse starter med å forberede et nytt kull. Ungene kan bruke et par år på å etablere seg i egne territorier, som så blir deres permanente tilholdssted.

Egg, unger og ungfugl er byttedyr for rødrever, coyoter, vaskebjørner, ville katter og huskatter. Det er nesten ingen som angriper voksne amerikahubroer, men de kan bli drept i konfrontasjoner med ørner, snøugler og andre amerikahubroer. Slike kamper kan ende med at seierherren spiser taperen.

Eksterne lenker

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Amerikahubro: Brief Summary ( норвешки )

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Amerikahubro (Bubo virginianus) er en ugle i gruppen Bubo. Den hører hjemme i både Nord- og Sør-Amerika, men er ikke fullt så vanlig som tårnuglen. Amerikahubro er aldri blitt observert i palearktis. Den er provinsfugl for den canadiske provinsen Alberta. Amerikahubro kan lett forveksles med Bubo magellanicus, som man en tid trodde tilhørte denne arten.

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Puchacz wirginijski ( полски )

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Commons Multimedia w Wikimedia Commons

Puchacz wirginijski (Bubo virginianus) – gatunek ptaka z rodziny puszczykowatych (Strigidae), zamieszkujący Amerykę Północną, Środkową i Południową. Teren lęgowy sięga od północnej granicy lasu na Alasce i w Kanadzie, przez Stany Zjednoczone, Meksyk, kraje Ameryki Środkowej. W Ameryce Południowej występuje w Wenezueli, Kolumbii, Peru, Boliwii, Brazylii, Paragwaju i Argentynie.

Występowanie

Puchacz wirginijski zamieszkuje zależnie od podgatunku[3][4][5]:

  • B. virginianus algistus – Alaska
  • B. virginianus lagophonus – środkowa Alaska do północno-wschodniego Oregonu, Idaho i północno-zachodniej Montany
  • B. virginianus saturatus – wybrzeża południowo-wschodniej Alaski do wybrzeży północnej Kalifornii
  • B. virginianus pacificus – wybrzeża środkowej Kalifornii do północno-zachodniej Kalifornii Dolnej
  • B. virginianus subarcticus – zachodnio-środkowa Kanada do północnego Idaho
  • B. virginianus pallescens – południowo-zachodnie USA do południowego Meksyku
  • B. virginianus pinorum – południowe Idaho do północnej Arizony i północnego Nowego Meksyku
  • B. virginianus heterocnemis – północno-wschodnia Kanada do obszaru Wielkich Jezior Północnoamerykańskich
  • B. virginianus virginianuspuchacz wirginijski – południowa-wschodnia Kanada do środkowego i wschodniego USA
  • B. virginianus elachistus – południowa Kalifornia Dolna
  • B. virginianus mayensis – półwysep Jukatan
  • B. virginianus mesembrinus – południowy Meksyk do zachodniej Panamy
  • B. virginianus nigrescens – Kolumbia do północno-zachodniego Peru
  • B. virginianus nacurutu – wschodnia Kolumbia przez Gujanę, północno-wschodnią Brazylię, Argentynę, Boliwię i środkowe Peru
  • B. virginianus magellanicuspuchacz magellański – środkowe Peru do Ziemi Ognistej, takson o niepewnej pozycji taksonomicznej, przez część systematyków traktowany jako odrębny gatunek[3][6].

Charakterystyka

Wygląd zewnętrzny
Największa sowa na kontynentach amerykańskich. Upierzenie w zależności od podgatunku występuje w różnych kolorach, od brązowego do jasnoszarego z licznymi ciemnymi plamami i kreskami. Głowa o dużych oczach, czarno obrzeżonych bokach twarzy i dwóch uszach z piór.
Rozmiary
długość ciała samca 51 cm, samicy 60 cm; rozpiętość skrzydeł samca 134 cm, samicy 143 cm[4]
Masa ciała
samiec 680-1450 g, samica 1000-2500 g[4]
Zachowanie
Aktywny głównie o zmierzchu i w nocy, rzadziej w dzień[4]. Łączą się w pary na całe życie. Najczęstszym odgłosem jest wydawany od 3 do 8 razy dźwięk uhu.
Długość życia
W niewoli do 38 lat, na wolności przeważnie 13 lat[7].

Środowisko

Lasy liściaste, mieszane i iglaste. Przebywa w zwartych drzewostanach, zagajnikach, małych laskach, dużych parkach miejskich.

Pożywienie

Poluje na małe i średnie ssaki (np. szczury, króliki i skunksy) i ptaki (np. inne sowy, krukowate, kaczki) oraz czasami na gady, płazy i duże owady.

Lęgi

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Trzy młode puchacze w gnieździe
Zachowania godowe
Sezon godowy i lęgowy trwa od stycznia do lutego. Podczas godów samiec o zmierzchu niezbyt głośno pohukuje.
Gniazdo
Stare gniazda ptaków drapieżnych lub krukowatych. Gniazduje również w dziuplach drzew, na występach skalnych, a nawet na ziemi lub w starych, opuszczonych budynkach.
Jaja i wysiadywanie
Samica składa 2 – 3 białe jaja (rzadko 5). Wysiaduje wyłącznie samica, samiec w tym czasie dostarcza pożywienie.
Pisklęta
Po około 35 dniach wylęgają się młode o gęstym, szarym puchu. Są karmione przez obydwoje rodziców. Młode uczą się latać po okołu siedmiu tygodniach życia. Dojrzałość płciową osiągają po dwóch latach.

Przypisy

  1. Bubo virginianus, w: Integrated Taxonomic Information System (ang.).
  2. Bubo virginianus. Czerwona księga gatunków zagrożonych (IUCN Red List of Threatened Species) (ang.).
  3. a b Frank Gill, David Donsker (red.): Family Strigidae (ang.). IOC World Bird List: Version 4.4. [dostęp 2014-11-05].
  4. a b c d Holt, W., Berkley, R., Deppe, C., Enríquez Rocha, P., Petersen, J. L., Rangel Salazar, J. L., Segars, K. P., Wood, K. L.: Great Horned Owl (Bubo virginianus). W: J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, E. de Juana (red.): Handbook of the Birds of the World Alive. Barcelona: Lynx Edicions, 2014. [dostęp 2014-11-05]. (ang.)
  5. Systematyka i nazwy polskie za: Paweł Mielczarek, Marek Kuziemko: Podrodzina: Striginae Leach, 1820 - puszczyki (Wersja: 2013-09-25). W: Kompletna lista ptaków świata [on-line]. Instytut Nauk o Środowisku Uniwersytetu Jagiellońskiego. [dostęp 2014-11-05].
  6. Holt, W., Berkley, R., Deppe, C., Enríquez Rocha, P., Petersen, J. L., Rangel Salazar, J. L., Segars, K. P., Wood, K. L.: Magellanic Horned Owl (Bubo magellanicus). W: J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, E. de Juana (red.): Handbook of the Birds of the World Alive. Barcelona: Lynx Edicions, 2014. [dostęp 2014-11-05]. (ang.)
  7. Great Horned Owl (Bubo virginianus) - Information, Pictures, Sounds - The Owl Pages, www.owlpages.com [dostęp 2017-11-26] (ang.).

Linki zewnętrzne

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Puchacz wirginijski: Brief Summary ( полски )

добавил wikipedia POL

Puchacz wirginijski (Bubo virginianus) – gatunek ptaka z rodziny puszczykowatych (Strigidae), zamieszkujący Amerykę Północną, Środkową i Południową. Teren lęgowy sięga od północnej granicy lasu na Alasce i w Kanadzie, przez Stany Zjednoczone, Meksyk, kraje Ameryki Środkowej. W Ameryce Południowej występuje w Wenezueli, Kolumbii, Peru, Boliwii, Brazylii, Paragwaju i Argentynie.

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Corujão-orelhudo ( португалски )

добавил wikipedia PT

A jacurutu (Bubo virginianus), também conhecida como corujão-orelhudo, jucurutu, mocho-orelhudo ou corujão-da-virgínia, é uma coruja de grande porte nativa das Américas. É uma ave extremamente adaptável com uma vasta distribuição, sendo a mais amplamente distribuída do continente.[2] Sua alimentação consiste em coelhos e lebres e ratos, apesar de caçar livremente qualquer animal que consiga, incluindo roedores e outros pequenos mamíferos, mamíferos de médio porte, aves, répteis, anfíbios e invertebrados. Em estudos ornitológicos, a jacurutu é frequentemente comparada ao bufo-real (Bubo bubo), uma espécie proximamente aparentada, que, apesar do tamanho notavelmente maior, ocupa o mesmo nicho ecológico na Eurásia, e ao búteo-de-cauda-vermelha (Buteo jamaicensis), com o qual frequentemente compartilha habitat, presas e hábitos de nidificação similares, sendo assim um equivalente ecológico durante o dia.[3] É uma das primeiras espécies a nidificar na América do Norte, pondo seus ovos semanas ou até meses antes de outras aves de rapina.[4]

Descrição

A jacurutu tem uma coloração para camuflagem,[4] sendo geralmente clara com faixas marrons por baixo e marrom-manchada, geralmente com marcações pesadas, complexas e mais escuras por cima. Todas as subespécies apresentam barras escuras em certa medida ao longo dos lados.

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Jacurutu com sua coloração e padrão camuflados

Uma mancha branca de tamanho variável é vista na garganta, podendo continuar como uma listra que desce até o meio do peito até quando as aves não estão em exibição e que em indivíduos particularmente pálidos pode ser ampliada como uma grande área branca na barriga. A subespécie B. v. nacurutu, que ocorre no Brasil, costuma apresentar essa mancha em tamanho reduzido, muitas vezes invisível, ao menos quando em exibição, e raramente exibe a área branca do peito.[3] Variações individuais e regionais na coloração geral existem, com os indivíduos do subártico apresentando uma cor amarela desbotada, enquanto aqueles da costa do Pacífico das Américas do Norte, Central e de grande parte da do Sul podem ter cor marrom-escura coberta com manchas pretas. As pernas, embora quase totalmente obscurecidas por penas, são pretas. As penas nas pernas da jacurutu são as segundas maiores conhecidas em qualquer coruja (atrás apenas das da coruja-das-neves).[3] O bico, assim como as garras, é cinza-metálico.[5]

Todos os indivíduos da espécie têm um disco facial, que pode ter coloração avermelhada, marrom ou cinza (dependendo das variações geográfica e racial) e que é demarcado por um arco escuro.[6] Os "chifres" são tufos de penas de propósito não totalmente entendido, embora a teoria de que estes sirvam como pistas visuais em interações territoriais e sociossexuais com outras aves seja geralmente aceita.[3]

Fisiologia e medidas

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O olho da jacurutu é um dos maiores entre os vertebrados terrestres

A jacurutu é a coruja mais pesada das Américas do Sul e Central e a segunda mais pesada da América do Norte, abaixo apenas da coruja-das-neves.[4][5] É robusta, com corpo em forma de barril, cabeça larga e asas grandes.[5] O tamanho pode variar consideravelmente através da distribuição geográfica, sendo as populações do interior do Alasca e Ontário maiores e as da Califórnia e do Texas menores, apesar de aquelas da Península de Yucatán e da Baixa Califórnia aparentarem ser ainda menores.[7][8] Os adultos chegam a medir de 43 a 64 cm de comprimento, sendo a média 55 cm, e 91 a 153 cm de envergadura de asas, sendo a média 122 cm. As fêmeas são um pouco maiores que os machos.[9][10] Em média, as fêmeas pesam 1608 g e os machos 1224 g.[11][12] Dependendo da subespécie, o peso máximo pode chegar a 2503 g.[13]

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Asas da jacurutu

O comprimento da corda máxima é de 297-400 mm.[14] A carga alar, a razão entre o peso da ave e a área da asa, é alta, o que significa que as asas são pequenas em relação ao peso, sendo descrita como a proporcionalmente mais alta entre as aves de rapina.[6][15] A cauda é relativamente curta, como é típico da maioria das corujas, medindo de 175 a 252 mm de comprimento. Assim como outras corujas, a jacurutu é capaz de realizar um voo silencioso, o modo pelo qual as corujas, apesar de seus grandes tamanhos, voam sem fazer nenhum barulho discernível. Isso é possível graças a três componentes principais da estrutura das asas: a ponta das penas de suas asas ser serrilhada, o que ajuda a interromper a turbulência gerada pelo bater das asas; as penas mais macias ajudarem a amortecer o som; e, por fim, as bordas das penas acabarem de eliminar os sons emitidos. A estrutura da asa da jacurutu também lhe permite voar em velocidades muito baixas para o tamanho da espécie, tão devagar quanto 3 km/h quando está planando no vento.[16]

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Jacurutu (Canadá)

As pernas, os pés e as garras são grandes e poderosos. O tarso mede 54-80 mm.[5] A envergadura do pé, quando totalmente aberto, de garra a garra, é de aproximadamente 20 cm, comparado a 8 cm na coruja-pequena, 13-15 cm na coruja-das-torres e 18 cm na coruja-lapônica.[3][17] A jacurutu consegue aplicar ao menos 300 psis de força com suas garras, uma pressão consideravelmente maior do que a mão humana consegue exercer. Em algumas fêmeas grandes, o poder de preensão pode ser comparado ao de aves de rapina muito maiores, como a águia-real.[18]

O bico, duro e inflexível, mede 3,3-5,2 cm de comprimento, apesar de o cúlmen, a parte exposta do bico medida ao longo da parte superior do bico, medir 2,1-3,3 cm.[19]

As aberturas externas das orelhas, que estão ocultas por penas nas laterais da cabeça, são relativamente menores do que as do bufo-real, medindo 2,3 cm no eixo vertical, com a orelha esquerda sendo um pouco maior que a direita.[20] Essa assimetria, existente na maioria das espécies exclusivamente (ou quase exclusivamente) noturnas, permite a triangulação dos sons escutados quando a coruja caça à noite e é suficiente para que a ave consiga usar o tempo e a direção das ondas do som que chegam em cada orelha para localizar a presa com precisão, mesmo se esta estiver embaixo de alguma cobertura como neve. O formato de disco do rosto também ajuda a direcionar os sons que são ouvidos para as orelhas. Embora a verdadeira natureza/propósito dos tufos de orelha que estão presentes na jacurutu seja desconhecida, os pesquisadores concordam que eles não desempenham nenhum papel na capacidade auditiva da ave. Estima-se que sua audição seja até dez vezes maior que a de um ser humano.[21]

Os olhos da jacurutu, apenas um pouco menores que os dos humanos, são grandes até mesmo para uma coruja e estão, proporcionalmente, entre os maiores olhos de todos os vertebrados terrestres.[22] Essa espécie possui olhos cilíndricos que criam mais distância entre a lente do olhos e a retina, permitindo assim o funcionamento destes como uma lente objetiva para distâncias maiores comparado com o que é possível com olhos redondos.[23] Essa espécie tem os olhos altamente adaptados para a caça noturna, que proporcionam um amplo campo de visão, quase completamente binocular, uma grande superfície da córnea e uma retina predominantemente de haste.[24] Os olhos contêm hastes e cones, assim como na maioria das espécies que vê cores, mas a visão se assemelha muito à de muitas outras espécies noturnas. O comprimento de onda máximo observado pelos cones é de 555 nm e a pesquisa sugere que a jacurutu tenha fraca visão de cores, especialmente comparado a outras espécies de ave. Apesar do pior senso de visão de cores (ou talvez devido a isso), a espécie tem ótima visão noturna.[25] Ao invés de virar os olhos, uma coruja precisa virar a cabeça toda, e a jacurutu consegue girar a cabeça em 270°. A íris é amarela, exceto na subespécie nacurutu (da América do Sul), na qual é âmbar.

Identificação da espécie

 src=
Comparação ilustrada de uma jacurutu, à esquerda, com seu parente norte-americano mais próximo, a coruja-das-neves

A combinação do porte, dos tufos de orelha proeminentes e da plumagem barrada da espécie distingue a jacurutu em grande parte de sua distribuição. Contudo, essa espécie pode ser facilmente confundida com Bubo magellanicus, com a qual pode haver sobreposição na área de ocorrência.[5] A última já foi considerada uma subespécie da primeira, mas atualmente é quase universalmente considerada uma espécie diferente, o que é apoiado pelo material genético, com a jacurutu sendo uma paraespécie.[5][6] A coloração geral é similar, mas B. magellanicus é notavelmente menor, com pés e cabeça menores, barras mais finas e mais numerosas por baixo, ao contrário das barras manchadas e irregulares de B. virginianus.[5] Outras espécies do gênero Bubo podem ser um pouco similares, mas a espécie é geralmente alopátrica, com exceção da coruja-das-neves durante o inverno. Espécies mais tropicais com tufos de penas nas orelhas, como o mocho-diabo (Asio stygius) e a coruja-orelhuda (A. clamator), são muito menores.[5] Outras corujas maiores não apresentam tufos de penas na orelha.[3]

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B. v. pallescens no topo de uma árvore-de-josué em Landers, Califórnia

Taxonomia

A jacurutu é uma espécie do gênero Bubo, que pode incluir outras 25 espécies viventes, distribuídas predominantemente na África.[6] Essa coruja é uma das uma ou duas radiações do gênero através da Beríngia para a América. Considerando Bubo magellanicus uma divisão da jacurutu quando esta já havia se espalhado pelo continente, o consenso parece ser que a coruja-das-neves e a jacurutu já tinham se dividido na Eurásia e a primeira se espalhou em volta do Ártico pelo extremo norte da América do Norte, separadamente da última.[5][26] A jacurutu e o bufo-real podem ser coespecíficos, com base em semelhanças em história natural, distribuição geográfica e aparência.[3] Em um caso, um macho de jacurutu e uma fêmea de bufo-real em cativeiro produziram um híbrido aparentemente saudável.[27] Testes genéticos indicaram que a coruja-das-neves, não o bufo-real, é a espécie vivente mais proximamente aparentada.[5] Foram encontrados na América do Norte fósseis do Pleistoceno de corujas do gênero Bubo que podem ser ou de uma espécie diferente ou de uma paleosubespécie, que existiria desde o oeste das Montanhas Rochosas, sendo predominante nelas, para o leste até a Geórgia.[9][28] Quase todos os fósseis indicam que essas corujas eram maiores que as atuais.[29][30]

Subespécies

 src=
B. v. nacurutu com seus olhos escuros
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B. v. subarcticus em Manitoba
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B. v. pacificus se alongando, Bernal Hill Park, São Francisco
 src=
B. v. pallescens com as penas molhadas esperando uma chuva no Deserto do Mojave
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Deserto do Mojave, B. v. pallescens no topo de uma árvore-de-josué no verão de 2018

Uma grande quantidade de subespécies, mais de 20 ao todo, foram descritas. No entanto, muitas destas não são subespécies verdadeiras, mas apenas exemplos de variação individual ou clinal. As diferenças entre as subespécies são principalmente na coloração e no tamanho e geralmente seguem as regras de Gloger e de Bergmann.[9] As classificações mais conservadoras de subespécies da jacurutu descrevem tão pouco quanto 10,[5] apesar de um número intermediário ser típico na maioria.[9]

  • Bubo virginianus virginianus (Gmelin, 1788)
Do Leste dos Estados Unidos para o oeste até pelo menos Minnesota e Texas; distribuição nordeste até o sul de Québec e de Ontário, na Nova Escócia e na Ilha do Príncipe Eduardo. Residente o ano inteiro.[9] A subespécie B. v. mesembrinus da América Central ao sul do Istmo de Tehuantepec, pode ser meramente uma subdivisão ao sul, uma vez que sua coloração é quase idêntica à de virginianus, apesar de o corpo ser levemente menor. No entanto, a distribuição de mesembrinus é descontínua, com as corujas mais pálidas pallescens e mayensis encontradas na distribuição intermediária, antes de virginianus reaparecer no sul do Texas.[5][8]
Apresenta coloração média, nem escura nem pálida. São conhecidos indivíduos de um cinza mais escuro ou um pouco mais pálidos. Tende a ser ricamente tingida de vermelho e com barras distintamente marrom-escuras por baixo com um contraste bastante suave. Os pés podem variar de castanho-amarelado a amarelo-claro a creme e as pernas são tipicamente barradas com cor escura a um grau moderado. O disco facial é frequentemente de cor sólida vermelho-acanelada. Apresenta um porte médio-a-grande, com a corda máxima medindo 319-371 mm, sendo a média 339 mm, nos machos e 343-388 mm, sendo a média 362,8 mm, nas fêmeas.[5][14][31] Inesperadamente, apesar de não ser a que possui a maior asa, esta subespécie é a mais pesada, com os machos pesando 985-1588 g, sendo a média 1318 g, e as fêmeas 1417-2503 g, sendo a média 1768,5 g; esses dados foram coletados em uma grande amostragem ao redor do Michigan. Em comparação, B. v. subarcticus, embora de asa maior, é em média um pouco menos pesada.[11][14] Por outro lado, na Costa Rica, dentro da área de ocorrência do possível sinônimo mesembrinus, essa subespécie pesa em média 1000 g, a massa mais leve relatada em qualquer lugar para esta espécie.[32] Outras medidas-padrão desta subespécie são a cauda de 190 a 235 mm, o comprimento do tarso de aproximadamente 56-58 mm e o bico de 35-50 mm.[5][11][14][31] B. v. virginianus também tende a ter os relativamente maiores tufos de orelha.[6]
  • Bubo virginianus nacurutu (Vieillot, 1817)
Subespécie que habita terras baixas e que ocorre em populações disjuntas desde o leste da Colômbia às Guianas; também no Brasil e no Uruguai ao sul da Bacia Amazônica até a Bolívia, na Província de Buenos Aires no norte da Argentina e no oeste do Paraguai. Residente o ano todo. Inclui as subespécies propostas scotinus, elutus, e deserti.[9][33][34] A condição desta subespécie, especialmente as relações entre as subpopulações dispersas e com a subespécie nigrescens e Bubo magellanicus, merece maiores estudos.
Pálida, de coloração típica marrom-terrosa; aves do interior semiárido do Brasil costumam apresentar branco na parte de cima da cauda. Menos -gato-listrado que nigrescens. É a única subespécie com íris âmbar, não amarela. Bubo magellanicus, embora um pouco semelhante na coloração, tem os olhos amarelos, assim como as outras subespécies. Médio porte, menor que a maioria das subespécies norte-americanas mas não tão pequena quanto algumas do México. A corda máxima mede 330-354 mm nos machos e 340-376 mm nas fêmeas. Em ambos os sexos a cauda pode atingir 184-217 mm de comprimento. Apenas três espécimes tiveram os seus pesos publicados, dois machos sendo um com 1011 g e outro com 1132 g e uma fêmea com 1050 g. A característica mais notável é o grande bico, que, apesar do tamanho moderado da subespécie, é o maior de todos, medindo de 43 a 52 mm de comprimento.[6][9][33]
  • Bubo virginianus subarcticus (Hoy, 1852)
Ocorre na época de reprodução na região de Mackenzie, na Colúmbia Britânica para o leste até o sul da Baía de Hudson; o limite sul é pouco claro, mas alcança pelo menos Montana e Dakota do Norte. Aves fora da temporada de reprodução são encontradas regularmente mais ao sul até o Paralelo 45 N, isto é, o Wyoming ou a Dakota do Sul, ultrapassando esse limite ocasionalmente principalmente nos anos com escassez de presas no norte. Essa subespécie inclui as aves descritas como occidentalis (baseada em indivíduo durante a invernada, assim como foi com o subarcticus original) e sclariventris.[35] O nome mais antigo wapacuthu foi usado às vezes para se referir a essa subespécie, contudo, não pode ser atribuído com certeza a um táxon reconhecível e assim é considerado um nomen dubium.[36] A população descrita como algistus é provavelmente baseada em indivíduos errantes e/ou vários híbridos de subarcticus com outras subespécies.[9][37]
Essa é a forma mais pálida de todas, com a coloração geral sendo essencialmente esbranquiçada com um leve tom amarelado por cima; barras pretas por baixo variando de indistintas a pronunciadas, sendo frequentemente mais proeminente no alto do peito entre plumagem de outro modo pálida. Essa subespécie mostra de pouco a nada de coloração avermelhada. Apresenta um grau muito alto de variação clinal, indo desde os Estados Unidos contíguos, onde as corujas são frequentemente meio-acinzentadas e mais fortemente marcadas, até a zona subártica no Canadá, onde são muito pálidas com marcas proeminentes quase inexistentes. Aves muito pálidas são, à distância, semelhantes a uma fêmea jovem de coruja-das-neves. Os pés variam do branco imaculado ao amarelo-claro, com pouca ou nenhuma mancha.[5][9] Pode hibridizar com as subespécies saturatus (no oeste) e heterocnemis (no leste), ambas de coloração escura. Nos dois casos, podem produzir híbridos de aparência intermediária de tom avermelhado, como um virginianus, mas com cores menos contrastantes.[38] É uma das maiores subespécies.[39] A corda máxima mede 323-372 mm, sendo a média 346,7 mm, nos machos e 339-390 mm, sendo a média 362,5 mm, nas fêmeas. Os machos pesam de 865 a 1460 g, sendo a média 1196,5 g, e as fêmeas de 1112 a 2046 g, sendo a média 1556 g. A cauda mede 200-225 mm e nos machos e 220-240 mm nas fêmeas. O bico mede de 35 a 43 mm de comprimento nos dois sexos e um espécime teve o tarso medido em 66 mm.[3][7][12][14][40][41]
  • Bubo virginianus pacificus (Cassin, 1854)
Sul e centro da Califórnia ao oeste da Serra Nevada exceto o Vale de San Joaquin, sul até noroeste de Baixa Califórnia, México. Encontra pallescens no Condado de San Diego, na Califórnia (ver abaixo). Residente o ano todo.[9]
Coloração marrom, barras escuras distintas por baixo, menos pronunciadas do que em saturatus mas mais pronunciadas do que em pallescens. A região do úmero é preta. Os pés são manchados de preto. O disco facial frequentemente apresenta manchas escuras.[9] É uma subespécie de pequeno porte, que inclui o indivíduo mais leve já pesado. A corda máxima mede 305-362 mm, sendo a média 332,5 mm, nos machos e 335-375 mm, sendo a média 351,4 mm, nas fêmeas. Os machos pesam de 680 a 1272 g, sendo a média 991,7 g, e as fêmeas de 825 a 1668 g, sendo a média 1312,7 g. A cauda mede 175-218 mm nos machos e 203-230 mm nas fêmeas. O bico mede 34-41 mm e um indivíduo teve o tarso medido em 57 mm.[3][7][12][14]
  • Bubo virginianus saturatus (Ridgway, 1877)
Ocorre na costa do Pacífico desde o sudeste do Alasca até o norte da Califórnia. Inclui o táxon descrito anteriormente B. v. leucomelas. A subespécie frequentemente reconhecida B. v. lagophonus é atualmente considerada muitas vezes uma mera variação clinal desta subespécie que ocorreria no interior do Alaska ao Oregon, no Rio Snake, e no noroeste de Montana.[9][38] Pode ser reportada no inverno para o sul até o Colorado e o Texas, mas estes registros são em tempos de migração.[34]
Subespécie escura e de coloração amarronzada no geral com a parte de baixo do corpo muito manchada, com uma base amarelada maçante. Aves do interior (lagophonus) tendem a ter a base mais acinzentada, enquanto as da costa são mais ricamente amarronzadas. A não ser por isso, aves da costa ou do interior são praticamente iguais. O disco facial pode variar de cinza a cinza-avermelhado a vermelho-escuro. O pés são completamente cinza-escuros, apesar de serem conhecidos alguns indivíduos com pés amarelo-claros, e as pernas sejam mais proeminentemente barradas de preto do que em outras subespécie norte-americanas.[5][9] Grande em medições lineares, sendo que os indivíduos do Alasca superam os de todas as outras subespécies, exceto heterocnemis em Ontário (que pode ser uma ala oriental descontínua desta subespécie). A corda máxima mede 330-370 mm, sendo a média 348,3 mm, nos machos e 339-400 mm, sendo a média 374,7 mm, nas fêmeas. A cauda mede de 191 a 245 mm nos machos e de 196 a 252 mm nas fêmeas. Nos dois sexos, os comprimentos de bico e do tarso são de 35-44 mm e 62-70 mm, respectivamente. Nenhuma medida de peso foi publicada.[3][7][12][14]
  • Bubo virginianus nigrescens (Berlepsch, 1884)
Andes; locais temperados áridos e com vegetação de puna desde a Colômbia até o noroeste do Peru. Residente o ano todo. Presumivelmente sinônimo do táxon descrito columbianus.[5]
Coloração escura, marrom-acinzentada, com manchas -gato-listrados fortes. Indiscutivelmente, esta é a subespécie mais escura, embora possa ser comparável nesse aspecto com indivíduos de saturatus e elachistus. Apresenta minimamente o tom castanho-avermelhado visto em outras subespécies escuras, apesar de alguns poderem ter um disco facial acanelado.[5] Esta é a subespécie de maior asa da América do Sul, com a corda máxima medindo 345-365 mm nos machos e 350-382 mm nas fêmeas. Nos dois sexos, a cauda mede de 185 a 217 mm. O bico mede 40-50 mm, sendo relativamente longo, assim como em nacurutu, e um indivíduo teve o tarso medido em 80 mm, indicando pernas relativamente longas. Não são conhecidas medidas de peso.[3][33] Aparentemente, apesar de sua asa de área considerável, nigrescens é notavelmente menor quando espécimes são comparados lado a lado com outros de saturatus.[5]
  • Bubo virginianus pallescens (Stone, 1897)
Vale do San Joaquin em direção ao sudeste através de regiões áridas do sudeste da Califórnia e do sul de Utah para o leste até o oeste do Kansas e para o sul até Guerrero e o oeste de Veracruz, no México; encontra pacificus no Condado de San Diego, e possivelmente em outros lugares; indivíduos vagantes de saturatus e da população das Montanhas Rochosas, que são semelhantes a híbridos, parecem ocorrer também na sua distribuição. Residente o ano todo.[9] Provavelmente sinônima de melanocercus.[5]
Coloração amarelo-escura pálida com barras indistintas, especialmente na parte de baixo do corpo. Indivíduos mais escuros tendem a ter uma base amarelada mais profunda em seus lados superiores. A área do úmero é âmbar e as penas dos pés são brancas e geralmente sem marcas.[5] De pequeno porte, é em média pouco maior no comprimento da asa do que pacificus, mas pesa menos em média. A corda máxima mede 318-367, sendo a média 337,2 mm, nos machos e 332-381 mm, sendo a média 348,9 mm, nas fêmeas. A massa varia de 724 a 1257 g, sendo a média 914,2 g, nos machos e de 801 a 1550 g, sendo a média 1142,2 g, nas fêmeas. Nos dois sexos, a cauda mede 190-235 mm e o bico 33-43 mm.[3][7][12][14]
  • Bubo virginianus mayensis (Nelson, 1901)
Endêmico dos dois-terços sul da Península de Yucatán. Residente o ano todo.
Uma forma meio-pálida, similar a pallescens nas marcações ventrais e na coloração. Em medições lineares, é menor do que todas as corujas norte-americanas, inclusive de pallescens, e é pouco maior que a subespécie seguinte.[3] A corda máxima e a cauda medem, respectivamente, 297-340 mm e 180-198 mm nos machos e 303-357 mm e 199-210 mm nas fêmeas. Nos dois sexos, o bico mede de 39 a 41 mm e o tarso de 54 a 65 mm.[8]
  • Bubo virginianus elachistus (Brewster, 1902)
Sul da Baixa Califórnia, México. Residente o ano todo.
Similar em cor a pacificus, mas escura e com barras mais fortes, como uma miniatura de saturatus. É consideravelmente (5–10%) menor que pacificus em medições lineares; embora ocorra alguma sobreposição de tamanho. É, em média, a menor subespécie conhecida. Nos machos, a corda máxima mede de 305 a 335 mm, a cauda de 175 a 206 mm e o bico de 33 a 38 mm. Uma única fêmea teve a corda máxima medida em 330 mm e a cauda em 211 mm.[5][8]
  • Bubo virginianus heterocnemis (Oberholser, 1904)
Reproduz-se no leste do Canadá (norte de Québec, Labrador, Terra Nova). O sul do seu limite de reprodução parece ser delineado pelo Rio São Lourenço.[38] No inverno, pode se dispersar para o sul através de Ontário até o nordeste dos estados Unidos. Poderia ser sinônima de saturatus, apesar de se distribuir longe para o leste desta. B. v. heterocnemis é cercada pela mais pálida subarcticus no leste e pela de marcas muito diferentes virginianus no sul, podendo se sobrepor com estas duas e possivelmente hibridizar.[34]
De coloração basicamente cinza e preta, fortemente barrada. Pés pálidos com manchas escuras. Em medições lineares relatadas (uma vez que a massa é desconhecida), esta é, em média, a maior subespécie. A corda máxima mede de 350 a 365 mm nos machos e de 370 a 390 mm nas fêmeas. Nos dois sexos, a cauda mede 220-250 mm e o bico 38-48 mm.[3][9][38]
  • Bubo virginianus pinorum (Dickerman & Johnson, 2008)
Montanhas Rochosas; reproduz-se ao sul do Rio Snake em Idaho, para o sul até Arizona, Novo México e as Mountanhas Guadalupe do Texas. Para o oeste, presume-se que ocorra no Platô de Modoc e no Lago Mono, na Califórnia. Foi incluída na subespécie presumida occidentalis, mas foi recentemente descrita e nomeada como uma subespécie distinta e constitui a peça que faltava na distribuição outrora confusa de jacurutus no oeste das e nas Montanhas Rochosas. Podem ocorrer movimentos de descida da montanha para vales ocupados por pallescens mas isto necessita de estudos.
Coloração cinza-média, intermediária entre saturatus e pallescens. Moderadamente barrada e tingida de amarelo-claro ou ocre na parte inferior. Pés manchados. Grande porte, com a corda máxima sendo inexplicavelmente maior nos machos, com 350-397 mm, que nas fêmeas, com 327-367 mm. A cauda mede de 190 a 233 mm e uma fêmea foi pesada em 1246 g.[9][42]

Distribuição e habitat

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Jacurutu em um celeiro, Ontário, Canadá

A jacurutu ocorre na maior parte das Américas do Norte e do Sul e muito irregularmente na América Central. Na porção mais austral da América do Sul, dá lugar à Bubo magellanicus, que ocupa todo o caminho para a Terra do Fogo, o extremo sul do continente. É ausente ou rara desde o sul de Guatemala, El Salvador, Nicarágua, e da Costa Rica ao Panamá (onde há apenas dois registros) e as florestas de mangue do noroeste da América do Sul. Também é ausente nas Índias Ocidentais, nas Ilhas da Rainha Carlota e em quase todas as ilhas das Américas, sendo assim a sua habilidade de colonizar ilhas aparentemente menor do que aquela da coruja-das-torres ou da mocho-dos-banhados.[3][32][34][43][44] Desde a sua divisão em duas espécies, é a segunda coruja mais amplamente distribuída das Américas, atrás apenas da coruja-das-torres.[5]

É uma das corujas ou até entre as aves mais adaptáveis do mundo quanto ao habitat, podendo fixar residência em árvores de vários tipos de vegetação, como florestas caducifólias, coníferas, decíduas temperadas e tropicais, pampas, pradarias, áreas montanhosas, desertos, tundra subártica, costas rochosas, mangues, e algumas áreas urbanas.[5] É menos comum nos lugares mais extremos das Américas. Nos desertos de Mojave e de Sonora, estão ausentes nas áreas mais secas e só são encontradas nas áreas vegetadas ou rochosas. Até na América do Norte, são raras em paisagens com mais de 70% de floresta primária, como nas florestas de faia das Montanhas Rochosas.[9][45] Foram registradas apenas poucas vezes em florestas tropicais como a Amazônia.[3] Nos Apalaches, aparentam usar a floresta primária,[46] mas no Arkansas são encontradas frequentemente próximas a aberturas agrícolas temporárias no meio de grandes áreas de floresta.[47] Assim como no centro-sul da Pensilvânia, usa terras agrícolas e pastagens mais do que coberturas totais de floresta decídua, indicando preferência por paisagens fragmentadas.[48] Em pradarias, campos e desertos, pode viver desde que existam cânions rochosos, ravinas íngremes e/ou barrancos arborizados com árvores que dão sombra para fornecer abrigo e locais de nidificação.[3][49]

Em áreas montanhosas da América do Norte, geralmente são ausentes acima da linha de árvores, mas podem ser encontradas até 2100 m na Califórnia e 3300 m nas Montanhas Rochosas.[3][50] Na Cordilheira dos Andes, por outro lado, adaptaram-se em uma espécie verdadeiramente montana, encontrada frequentemente a pelo menos 3300 m acima do nível do mar e são registradas regularmente na região sem árvores da puna entre os 4100 e 4500 m de altitude no Equador e no Peru.[51] São geralmente raras em habitats de pântanos sem marés,[52] e são substituídas na tundra ártica pela coruja-das-neves.[5] Prefere áreas onde habitats abertos (nos quais muitas vezes caça) e bosques (onde tende a se empoleirar e a nidificar) estão justapostos.[53][54][55] Assim, regiões rurais pouco povoadas podem ser ideais. Esta espécie pode ocasionalmente ser encontrada em áreas urbanas ou suburbanas. Contudo, nestes espaços ela aparenta preferir áreas com menos atividade humana e é mais provavelmente encontrada em configurações como parques, ao contrário das corujas Megascops asio e M. kennicottii, que podem ocorrer regularmente em ambientes suburbanos movimentados. Todas as jacurutus acasaladas são residentes permanentes de seus territórios, mas indivíduos solteiros e jovens movimentam-se livremente em busca de companhia e territórios, e deixam áreas com pouco alimento no inverno.[5]

Comportamento

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Foto composta que mostra as fases do voo da jacurutu
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Jacurutus são tipicamente vagarosas e passivas durante o dia, mas atentas

Grande parte dos aspectos do comportamento da jacurutu é típico de outras corujas e da maioria das aves de rapina. Pela criação experimental de jovens em cativeiro, Paul L. Errington sentiu que esta era uma ave de "inteligência essencialmente baixa" que podia caçar apenas quando parcialmente selvagem e instintivamente movida pela fome para caçar a primeira presa que encontrasse. Ele mostrou que indivíduos em cativeiro que recebiam carne desde o nascimento, ao invés de terem que caçar ou simular uma caça para obter comida, não tinham essa capacidade.[56] Pelo contrário, William J. Baerg comparou suas jacurutus cativas criadas de modo comportamental a papagaios, aves famosamente inteligentes. Embora não sejam tão frequentemente brincalhonas, elas "conhecem seu guardião e geralmente aceitam tudo o que ele deseja fazer com uma boa dose de tolerância".[57] Arthur C. Bent também notou a variabilidade nos temperamentos de jacurutus quanto aos seus treinadores, algumas geralmente simpáticas, apesar da maioria ser eventualmente agressiva.[4] A maioria dos espécimes em cativeiro, uma vez maduros, parece ressentir-se com tentativas de contato e são frequentemente dados a atacar seus guardiões. Vão seguir pistas apenas se condicionadas desde jovens, mas raramente no mesmo nível de sucesso que é visto em algumas aves de rapina diurnas quando treinadas para falcoaria ou entretenimento, embora isso não esteja necessariamente relacionado à inteligência, como proposto por Errington.[56][57] Carl D. Marti também discorda das observações de Errington, notando que a sua seleção de presas não é "completamente aleatória como Errington sugeriu"; e sim "aparentando selecionar as suas presas mamíferas em relação geral com as populações destas. Coelhos-de-cauda-de-algodão parecem ser selecionados como presa em relação ao seu status populacional."[17]

Assim como a maioria das corujas, a jacurutu faz ótimo uso da discrição. Devido à sua plumagem de cor natural, camufla-se bem quando ativa à noite e quando descansa durante o dia. Durante o dia costuma descansar em árvores grandes (incluindo protuberâncias e grandes ocos, mas geralmente galhos grossos) mas pode ficar ocasionalmente em fendas ou pequenas cavernas em rochas ou arbustos densos. Pinheiros e outras coníferas podem ser preferidos quando estão disponíveis desde que particularmente densos e forneçam cobertura ao longo do ano. Tipicamente, os machos têm um poleiro não distante dos ninhos, algumas vezes usado por anos sucessivos.[58] Quando empoleiradas, estas aves podem descansar em uma posição na qual ficam eretas e o mais finas possível. O tipo de postura é conhecido como um método adicional de camuflagem para corujas, como a coruja-pequena e a coruja-lapônica, especialmente se humanos ou outros mamíferos potencialmente carnívoros se aproximam delas. O bufo-real assume essa posição raramente ou nunca.[59] Fora da temporada de nidificação, pode se empoleirar onde quer que seu trajeto de forrageamento termine ao amanhecer.[60] São geralmente ativas à noite, mas em alguns lugares podem ser ativas no fim da tarde ou no início da manhã. No crepúsculo, realiza algumas vocalizações antes de voar para um lugar mais aberto, isto é, um grande galho descoberto ou grandes pedras, para cantar. Normalmente são usados vários poleiros para marcar o território ocupado ou para atrair uma fêmea.[5] Apesar de sua camuflagem e de gostar de lugares ocultos, pode ser vista algumas vezes nos seus poleiros de passar o dia, principalmente por corvos-americanos (Corvus brachyrhynchos). Uma vez que estas corujas são, ao lado do búteo-de-cauda-vermelha, talvez a principal predadora de corvos e seus jovens, estes algumas vezes se juntam de uma distância considerável para atacar e grasnar para elas por horas a fio. Quando as corujas tentam voar para evitar este assédio, são muitas vezes perseguidas pelos corvos.[61]

Territorialidade e movimentos

As jacurutus são tipicamente sedentárias, frequentemente capazes de utilizarem um único território por toda a sua vida adulta.[62] Apesar de algumas espécies como a coruja-das-neves, a coruja-serra-afiada, a coruja-pequena e a mocho-dos-banhados serem verdadeiramente migratórias, a maioria das corujas norte-americanas não o são e costumar ser fiéis a um único território por todo o ano.[3] Os casais ocupam territórios por todo o ano e por um longo prazo. Os territórios são estabelecidos e mantidos por meio de vocalizações, com a maior atividade sendo antes da postura de ovos e no outono, quando os jovens dispersam, e podem medir em média de 2,1 km2 no Wyoming até 16 km2 em Yukon.[11][60]

A maior parte da defesa do território é realizada pelos machos, mas as fêmeas costumam ajudar seus parceiros em disputas de vocalização com vizinhos e intrusos, até mesmo durante a incubação.[9] Apesar de os limites do território serem mantidos com sucesso através apenas de vocalizações sem nem mesmo ver a coruja oponente, tais confrontos podem se tornar físicos, com vários níveis distintos de ameaça. O nível de ameaça mais alto envolve o abrir de asas, bater do bico, assobios, gritos agudos de longa duração, com o corpo em geral pronto para golpear o intruso com os pés. No caso de o intruso continuar confrontando, a coruja defensora dá um "salto" para a frente e atinge o oponente com os pés, tentando agarrá-lo com as garras.[9]

A territorialidade parece colocar um limite no número de pares reprodutores em uma determinada área. Indivíduos impedidos de estabelecer um território vivem uma existência silenciosa como "flutuadores". A radiotelemetria revelou que tais flutuadores se concentram ao longo dos limites de territórios já estabelecidos. No Lago Kluane, em Yukon, incursões em territórios vizinhos foram observadas apenas duas vezes — por fêmeas quando a fêmea vizinha morreu ou emigrou, o que sugere que a defesa do território pode ser específica do sexo. Pelo menos quatro indivíduos morreram em Kluane aparentemente mortas por outros de sua própria espécie em conflitos de território.[60] Corujas mortas por outras da mesma espécie são algumas vezes canibalizadas, embora a morte possa ter sido por causa de agressão por território.[63] As populações mais setentrionais irrompem ocasionalmente no sul durante épocas de escassez de alimentos,[64] mas não há migração anual até no limite norte da distribuição da espécie.[60]

Comportamento de caça

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Close nas garras da jacurutu

O pico da atividade de caça tende a ser entre as 20:30 e a meia-noite e então pode retornar das 04:30 ao nascer do sol.[65] A caça também costuma ser mais prolongada durante o inverno devido à escassez de presas.[66] No entanto, a jacurutu pode aprender a ter uma certa presa como alvo durante a tarde quando esta estiver mais vulnerável, como o esquilo Sciurus niger enquanto constrói os seus ninhos e a iguana Sauromalus ater quando toma sol nas rochas do deserto.[67][68] Caça principalmente por meio da observação a partir de um poleiro alto. Durante as incursões de caça, costuma voar cerca de 50 a 100 m de poleiro a poleiro, parando para procurar alimento em cada um, até que percebam uma presa. A partir de tais pontos de vista, a coruja desce até o solo, frequentemente com as asas fechadas, para emboscar a presa.[5] A distância máxima de caça a partir de um poleiro elevado é de 90 m.[69] Devido às suas asas pequenas, mas amplas, essa espécie é adequada para baixa velocidade e capacidade de manobra.[15] Apesar de relatos de que não caça com as asas,[70] algumas vezes o faz voando baixo sobre aberturas no chão, procurando por atividade de presas.[5] Pode alcançar velocidades de mais de 65 km/h em voo nivelado.[3] Os voos para caça são devagar, muitas vezes bem acima do solo, onde a presa pode ocorrer em campo ou floresta abertos. O voo pairado breve (de aproximadamente 6–18 segundos) foi descrito, principalmente em áreas com vento.[71] Também pode ocasionalmente caçar andando no chão em perseguição a presas de pequeno porte ou, raramente, dentro de um galinheiro para atacar as aves dentro deste.[10] Roedores e invertebrados podem ser pegos a pé em torno da base de arbustos, através de áreas gramadas e perto de bueiros e outras estruturas humanas como fazendas.[9] Essa espécie não anda bem no solo: caminha como um estorninho, com uma maneira de andar lado-a-lado pronunciada. É conhecida por entrar em águas rasas para procurar presas aquáticas, embora isso tenha sido raramente relatado.[9] Pode apanhar aves e alguns mamíferos arbóreos diretamente dos galhos das árvores ou também em voo planado. As penas rígidas de suas asas permitem que produzam um som mínimo durante o voo.[2][5][10]

Quase todas as presas são mortas por esmagamento com os pés ou por serem incidentalmente apunhaladas com as garras, embora algumas também possam ser mordidos no rosto. A presa é engolida inteira quando possível e, quando isso acontece, a coruja regurgita plumadas com ossos e outros pedaços não-digeríveis aproximadamente 6 a 10 horas depois, geralmente no mesmo local onde a presa é consumida.[5] Essas plumadas são de cor cinza-escura ou marrom e muito grande, com 7,6 a 10,2 cm de comprimento e 3,8 cm de espessura, e são conhecidas por terem crânios de 3 cm de largura dentro delas.[10] Contudo, nem todas as presas podem ser engolidas de uma só vez, e desse modo as corujas voam com estas até um poleiro e arranca pedaços com o bico. A maioria dos estudos da dieta da espécie foca nas plumadas encontradas embaixo dos poleiros e ao redor dos ninhos, uma vez que estas proporcionam uma visão da diversidade das presas que são consumidas, mas restos da presa fora das plumadas podem fornecer pistas para presas excluídas destas. Assim, é recomendada uma combinação dos dois métodos.[3][72][73] Muitas presas de grande porte são desmembradas. A jacurutu pode tirar a cabeça de presas grandes antes de levá-las ao ninho ou ao poleiro onde vai consumi-la. As pernas também podem ser removidas, assim como as asas (em aves). Essa espécie também esmaga os ossos da presa para fazê-la mais compacta para carregar.[74] Ocasionalmente, as corujas podem retornar ao lugar da morte da presa e continuar a comê-la se esta for muito pesada para ser carregada em voo após o desmembramento.[4] Muitas corujas acumulam um esconderijo de presas, em especial aquelas que estão nidificando. Estes devem ser em um local seguro, geralmente uma forquilha em uma árvore alta. Nas regiões mais ao norte, onde presas maiores prevalecem, pode deixar o alimento que não foi consumido congelado e descongelá-lo mais tarde com o calor de seu próprio corpo.[6] O sucesso da caça parece necessitar de sub-bosque razoavelmente aberto, e testes experimentais de micro-habitat provaram que áreas abertas proporcionaram maior sucesso na caça de cinco espécies de roedor, com noites nubladas e folhagem de arbusto mais densa diminuindo-o.[75]

Alimentação

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Pintura de Louis Agassiz Fuertes mostrando uma jacurutu com uma de suas principais presas, a lebre-americana

As presas podem variar muito, em função da oportunidade. De acordo com um autor, "quase qualquer criatura viva que anda, rasteja, voa ou nada, exceto os grandes mamíferos, é uma presa legítima da jacurutu".[18] Na verdade, a jacurutu tem o perfil de presas mais diverso entre todas as aves de rapina da América.[3] Já foram identificadas mais de 500 espécies predadas por esta coruja, com mais dúzias identificadas apenas o gênero ou aparência geral (especialmente numerosos invertebrados), e presumivelmente mais várias desconhecidas da sua população relativamente pouco estudada nos Neotrópicos. Mamíferos (mais de 200 espécies) e aves (em torno de 300 espécies) constituem a maior parte de sua dieta.[3][72] Sua dieta na América do Norte é constituída em 87,6% por mamíferos, 6,1% por aves, 1.6% por répteis e anfíbios e os 4,7% restantes por insetos, diversos outros invertebrados e peixes.[3] A massa estimada de cada presa da jacurutu vaeia de 0,4 g até 6,8 kg.[76][77] A maioria das presas está entre 4 g (musaranhos) e 2300 g (lebres).[76][78] Um único indivíduo necessita aproximadamente de 50 a 100 g de comida por dia e pode subsistir com uma grande caça por vários dias.[79] Apesar da grande diversidade de presas dessa espécie, na maior parte dos Estados Unidos Continentais, do leste ao meio-oeste, assim como no Canadá e no Alasca, vive em grande parte de poucas espécies: três lagomorfos - o coelho-da-flórida (Sylvilagus floridanus), a lebre-americana (Lepus americanus) e a lebre-da-califórnia (L. californicus); duas espécies de ratos do gênero Peromyscus: o rato-veadeiro (Peromyscus maniculatus) e P. leucopus; três espécies de rato-do-campo: o arganaz-do-campo (Microtus ochrogaster), M. pennsylvanicus e M. pinetorum e uma peste introduzida, o rato-marrom.[9][72][76]

Reprodução

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Filhotes de jacurutu nas Montanhas Rochosas no Novo México (B. v. pinorum)
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Juvenis da subespécie B. v. saturatus próximos ao Refúgio Nacional de Vida Silvestre do Lago Tule, Oregon, Estados Unidos

A jacurutu é uma das aves da América do Norte que começa a sua reprodução mais cedo, aparentemente em parte por causa do longo anoitecer nesta época do ano e, adicionalmente, a vantagem competitiva que isso dá sobre outras aves de rapina. Na maior parte da América do Norte, o cortejo ocorre de outubro a dezembro e os casais são formados de dezembro até janeiro.[5] Pensava-se que esta espécie era estritamente monogâmica, mas análises recentes indicaram que um macho pode acasalar com duas fêmeas simultaneamente, como foi descoberto em Reno, Nevada, no ano de 2018.[80] Durante o cortejo no final do outono ou no início do inverno, o macho atrai a atenção de seu par vocalizando enfaticamente enquanto se inclina (com a cauda fechada ou aberta) e estufando a garganta branca para que esta pareça uma bola.[5] A garganta branca pode servir como um estímulo visual em condições de pouca luz típicas de quando o cortejo acontece.[60] O macho frequentemente voa para cima e para baixo em um poleiro, enquanto se aproxima de uma potencial parceira. Eventualmente, chega perto da fêmea e tenta esfregar o seu bico contra o dela enquanto se curva repetidamente. Se for receptiva, a fêmea vocaliza quando se encontra com o parceiro, mas é mais subjugada nos cantos e na exibição. O macho pode convencer a fêmea levando-a alimento fresco, que ambos compartilham.[4][5] Enquanto os machos costumam vocalizar enfaticamente por cerca de um mês ou seis semanas no final do ano, o período em que as fêmeas também vocalizam é geralmente de apenas uma semana a dez dias.[81] Os casais costumam procriar ano após ano e podem ficar juntos para o resto da vida, embora eles se associem uns com os outros mais livremente quando seus filhos se tornam independentes.[5] Pares que reacendem sua relação reprodutiva no inverno podem realizar um cortejo mais moderado para fortalecer os laços antes de produzir filhotes.[81]

O macho seleciona os locais de nidificação e chama a atenção das fêmeas para ele voando em sua direção e pisando nelas.[5] Devido ao grande tamanho desta ave, são preferidos ninhos abertos em vez de cercados com ramos circundantes. Assim como todas as corujas, a jacurutu não constrói o seu próprio ninho, tendendo a examinar a área em busca de um ninho abandonado, geralmente de aves de grande porte, como gaviões, e assume o controle para criar seus próprios filhos.[82] É a ave norte-americana que nidifica na maior variedade de habitats.[81] Muitos ninhos ficam em cavidades cavernosas de árvores mortas ou seus galhos, especialmente nos estados do sul dos Estados Unidos, em grandes árvores ao longo da borda de florestas primárias.[81] Em áreas montanhosas, especialmente em cânions do sudeste dos Estados Unidos e nas Montanhas Rochosas, saliências de penhascos, cavernas pequenas, e outras depressões protegidas podem ser usadas.[81] Quando vivendo em pradarias, na ausência de ninhos de outros animais, usando árvores ribeirinhas ou não nativas ou o solo descoberto de ocos de árvores ou estruturas feitas pelo homem, pedras, montículos, cortes de ferrovia, arbustos baixos e até mesmo o solo descoberto como locais de nidificação.[81] Ninhos no solo também foram registrados no meio de gramíneas altas na Flórida e de manchas de arbustos no solo do deserto.[3] Até as entradas das tocas de texugo-americano e de coiote são usadas como ninhos, apesar do risco inerente de compartilhar espaço com coabitantes potencialmente perigosos.[81] O comportamento de nidificação parece ter relação mais forte com a disponibilidade de presas do que como condições sazonais.[81] Há algumas evidências de que, se a disponibilidade de presas for baixa o suficiente, a espécie pode renunciar ao acasalamento a temporada inteira. Indivíduos de ambos os sexos já foram observados incubando os ovos assim que estes foram postos.[83]

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Uma fêmea de jacurutu em seu ninho em Louisiana, Estados Unidos

A maioria dos ninhos em árvores usados pela jacurutu são construídos por outros animais, frequentemente entre os 4,5 e 22 m de altura. Ela costuma assumir o ninho usado por outra ave de grande porte, adicionando às vezes penas para forrar o ninho, mas geralmente não muito mais. Supostamente, há alguns casos em que o ninho foi reconstruído ou teve a sua estrutura reforçada, mas como regra nenhuma coruja jamais foi conhecida por realmente construir o ninho.[81] No sudoeste dos Estados Unidos também pode usar ninhos em cactos, construídos pelo gavião-asa-de-telha ou pelo búteo-de-cauda-vermelha, bem como grandes cavidades nestas plantas.[84] Os ninhos usados são frequentemente feitos por accipitrídeos de grande porte, desde espécies tão pequenas quanto o falcão-do-tanoeiro até a águia-careca e a águia-real, embora os mais frequentes sejam talvez os de búteos-de-cauda-vermelha e outros Buteoninae. Os segundos em popularidade são os de corvos (Corvus sp.). Além disso, já foram usados ninhos de ganso-do-canadá, savacu e garça-azul-grande, a última às vezes bem no meio de uma colônia ativa.[85][86] Os ninhos de folhas feitos por esquilos também são usados regularmente, mas são preferidos em geral ninhos de gravetos, uma vez que estes fornecem uma base muito mais firme e segura.[9]

A época do ano na qual os ovos são postos é variável na América do Norte. No sul da Flórida, a postura ocorre desde o final de novembro até o início de janeiro. No sudeste dos Estados Unidos, do sul do Texas até a Geórgia, desde o final de dezembro até o início de fevereiro. Do sul da Califórnia até o norte de Louisiana, desde o início de fevereiro até o final de março. O maior período é desde o final de fevereiro até o início de abril, na região do centro da Califórnia até a Carolina do Sul para o norte até Ohio e Massachusetts. Nas Montanhas Rochosas, no noroeste dos Estados Unidos, no norte da Nova Inglaterra e no leste do Canadá, a postura ocorre desde o início de março até o final de abril. No resto do Canadá e no Alasca, pode ocorrer do final de março até o início de maio.[81] A data mais tardia conhecida para a postura é em meados de junho em Saskatchewan e Yukon.[87] No noroeste de Utah e no centro-norte de Alberta, a postura pode acontecer 3–4 semanas mais cedo quando há abundância de alimento e o clima é favorável.[9] Em climas mais tropicais, as datas da temporada de reprodução são de algum modo indefinidas.[5] Geralmente há dois ovos por ninhada, podendo variar de um a seis (acima de três é incomum e acima de quatro é muito raro), dependendo de condições ambientais.[88][89] Um ovo mede em média 46,5 mm de largura, 55 mm de comprimento e pesa 51 g, embora a massa possa ser levemente mais alta em outros lugares, uma vez que este levantamento foi realizado no Condado de Los Angeles, na Califórnia, onde as corujas são relativamente pequenas.[90] A incubação dura entre 28 e 37 dias, sendo a média 33 dias.[91] A fêmea geralmente é a única responsável pela incubação e raramente sai do ninho, enquanto o macho caça e leva o alimento para ela, com a primeira entrega de comida à noite normalmente ocorrendo logo após o anoitecer.[9]

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Jacurutu em seu ninho, nas proximidades de Madison, Wisconsin

O filhote recém-nascido pesa em torno de 34,7 g e pode ganhar em média 33,3 g por dia nas primeiras quatro semanas de vida, com o peso típico com 25-29 dias sendo de 800 g nos machos e de 1000 g nas fêmeas.[90][91] Quando eclodem, os filhotes têm penugem cinza-esbranquiçada, com um pouco de marrom nas asas. Gradualmente, a plumagem aveludada juvenil passa pela penugem, sendo tipicamente uma amarelo-canela, mas com matizes variáveis, prevendo a eventual cor das corujas maduras. A extensão da penugem diminui gradualmente, desenvolvendo plumagem de aparência madura no final do verão, embora muitas aves do primeiro ano ainda tenham pedaços espalhados de penugem no outono. No final do outono, aves de primeiro ano têm aparência similar à dos adultos mas com um tom ligeiramente mais avermelhado, tufos de orelha menos desenvolvidos e uma mancha branca menor na garganta.[4] Os filhotes se desenvolvem principalmente no comportamento entre duas semanas e dois meses de idade, período em que adaptam a capacidade de se defender, agarrar alimentos e escalar. Vocalmente, os jovens são capazes de exercer sons fracos enquanto ainda está no ovo, que se desenvolvendo em um chiado rouco logo após a eclosão. Os chamados dos jovens aumentam rapidamente em intensidade, tom e características; alguns jovens do sexo masculino imitam a vocalização do pai no outono, mas geralmente concluem com várias notas gorgolejantes estranhas. O primeiro canto normal do juvenil não acontece antes de janeiro.[9][92] Os jovens mudam-se para galhos próximos às seis semanas e começam a voar cerca de uma semana depois. No entanto, geralmente não voam bem até que tenham em torno de 10 a 12 semanas de vida.[5] A idade na qual o juvenil sai do ninho é variável com base na abundância de alimento.[93]

Os jovens ficam em uma área entre 13,1 e 52 ha do ninho no outono, mas geralmente dispersam em milhares de hectares no final desta estação.[94][95] Os filhotes ainda pedem comida aos pais no final de outubro (cinco meses após saírem do ninho) e a maioria não deixa o território dos pais até pouco antes de os pais começarem a se reproduzir para a próxima ninhada (geralmente entre dezembro e janeiro).[96] Algumas aves podem não se reproduzir por um ano ou dois, e são frequentemente vagantes ("flutuadores") até que estabeleçam seus próprios territórios.[60] Com base no desenvolvimento da bursa, a jacurutu atinge a maturidade sexual aos dois anos de idade.[97]

Iconografia e mito

Muitos tribos guerreiras nativas dos Estados Unidos admiravam a jacurutu por sua "força, coragem e beleza".[79] Os Pima, povo do sudoeste dos Estados Unidos acreditavam que esta coruja era a reencarnação de guerreiros mortos que voam à noite. Os Arikara das Grandes Planícies tinham uma sociedade mística na qual os iniciados eram obrigados a adornar máscaras faciais feitas de penas da cauda e da asa da jacurutu. Algumas nações indígenas consideravam a jacurutu um espírito amigável que poderia ajudar em questões amorosas, como os Passamaquoddy do Maine, que pensavam que o chamado desta espécie era uma flauta mágica do amor projetada para inflamar as paixões humanas. Os Hopis, do sudoeste dos Estados Unidos, também associaram essa coruja com a fertilidade, embora de um tipo diferente: eles acreditavam que a vocalização desta coruja no verão previa um clima quente, o que produzia boas safras de pêssego. Durante o solstício de inverno, este povo realizava uma cerimônia com penas de jacurutu na esperança de convocar o calor do verão. Tribos do Novo México são conhecidas por usar as penas das asas da jacurutu para produzir flechas que podiam atingir seus inimigos com um mínimo de som. Os Zuni seguravam as penas da coruja em suas bocas na esperança de obter um pouco do silêncio que as corujas usam em emboscadas enquanto atacavam seus inimigos de outras tribos. Os Iroqueses pensavam que a origem da jacurutu era devido a uma coruja imatura que irritava Raweno, o criador todo-poderoso, enquanto este criava os coelhos, fazendo este deixar a coruja "coberta de lama" (camuflagem escura) e condenada a ter uma incessante vocalização de "whoo-whoo", que usava para assediar Raweno à noite, porque este era ativo durante o dia.[79]

Ave provincial

A jacurutu é a ave provincial de Alberta, no Canadá.[98]

Referências

  1. BirdLife International (2014). «Bubo virginianus». Lista Vermelha da IUCN. 2014. p. e.T61752071A61752159. doi:10.2305/IUCN.UK.2014-2.RLTS.T61752071A61752159.en
  2. a b «Great Horned Owl». The Cornell Lab of Ornithology. Consultado em 21 de Março de 2013. Cópia arquivada em 5 de Julho de 2017
  3. a b c d e f g h i j k l m n o p q r s t u v w x y Voous, K.H. 1988. Owls of the Northern Hemisphere. The MIT Press, 0262220350.
  4. a b c d e f g Bent, A. C. 1938. Life histories of North American birds of prey, Part 2. U.S. National Museum Bulletin 170:295-357.
  5. a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al König, Claus; Weick, Friedhelm (2008). Owls of the World 2ª ed. London: Christopher Helm. ISBN 9781408108840
  6. a b c d e f g Owls of the World: A Photographic Guide by Mikkola, H. Firefly Books (2012), ISBN 9781770851368
  7. a b c d e Mcgillivray, W. B. 1989. Geographic variation in size and reverse size dimorphism of the Great Horned Owl in North America. Condor 91:777-786.
  8. a b c d Webster, J. D. and R. T. Orr. 1958. Variation in the Great Horned Owls of Middle America. Auk 75:134-142.
  9. a b c d e f g h i j k l m n o p q r s t u v w x y z Houston, C. Stuart, Dwight G. Smith and Christoph Rohner. 1998. Great Horned Owl (Bubo virginianus), The Birds of North America Online (A. Poole, Ed.). Ithaca: Cornell Lab of Ornithology; Retrieved from the Birds of North America Online.
  10. a b c d «Great Horned Owl – Bubo virginianus – Information, Pictures, Sounds». Owlpages.com. Consultado em 9 de fevereiro de 2012
  11. a b c d Craighead, J. J. and F. C. Craighead, Jr. 1956. Hawks, owls and wildlife. Stackpole Co. Harrisburg, PA.
  12. a b c d e Snyder, N. F. R. and J. W. Wiley. 1976. Sexual size dimorphism in hawks and owls of North America. AOU Ornithological Monograph, 20:1-96.
  13. CRC Handbook of Avian Body Masses by John B. Dunning Jr. (Editor). CRC Press (1992), ISBN 978-0-8493-4258-5.
  14. a b c d e f g h Earhart, C. M. and N. K. Johnson. 1970. Size dimorphism and food habits of North American Owls. Condor 72:251-264.
  15. a b Johnson, D. H. 1998. Wing loading in 15 species of North American owls. Pages 553-561 in Biology and conservation of owls of the Northern Hemisphere, 2nd International Symposium, 5–9 February 1997, Winnipeg, Manitoba. (Duncan, J. R., D. H. Johnson, and T. H. Nicholls, Eds.) U.S. Dept. of Agriculture Forest Service, North Central Forest Experiment Station, Gen. Tech. Rep. NC-190, St. Paul, MN
  16. «The Silent Flight of Owls, Explained». Audubon (em inglês). 28 de julho de 2017. Consultado em 21 de fevereiro de 2020
  17. a b Marti, C. D. (1974). Feeding ecology of four sympatric owls. Condor, 45-61.
  18. a b Lee, Carol (26 de Março de 2006). «Powerful feet and talons help birds of prey make their living». Lubbock Avalanche-Journal. Consultado em 21 de Março de 2013
  19. Ridgway, R. 1914. Birds of North and Middle America. Bulletin of the U.S. National Museum, No. 50. Pt. 6.
  20. Norberg, R.A. 1977. Occurrence in independent evolution of bilateral ear asymmetry in owls and implications in owl taxonomy. Philosophical Transaction Royal Society, London, Biological Science, 280 (973): 375-408.
  21. Traynor, Robert M. (Setembro de 1997). «The missing link for success in hearing aid fittings». The Hearing Journal. 50 (9). p. 10. ISSN 0745-7472. doi:10.1097/00025572-199709000-00001
  22. Hall, M. I., & Heesy, C. P. (2011). Eye size, flight speed and Leuckart's Law in birds. Journal of Zoology, 283(4), 291-297.
  23. WALEED (24 de agosto de 2018). «Great Horned Owl Eyes – How Far Can a Great Horned Owl See?». Great Horned Owl (em inglês). Consultado em 21 de fevereiro de 2020
  24. Fite, K. V. 1973. Anatomical and behavioral correlates of visual acuity in the Great Horned Owl. Vision Research; 13:219-230.
  25. Jacobs, Gerald H.; Crognale, Michael; Fenwick, John (Maio de 1987). «Cone Pigment of the Great Horned Owl». The Condor. 89 (2). 434 páginas. doi:10.2307/1368502
  26. Potapov, E., & Sale, R. (2013). The Snowy Owl. Poyser Monographs, A&C Black.
  27. Risdon, D.H.S., 1951. The rearing of a hybrid Virginian x European Eagle-Owl at Dudley Zoo. Avicultural Magazine, 57: 199-201.
  28. Brodkorb, P. 1971. Catalogue of fossil birds, Part 4 (Columbiformes through Piciformes). Bulletin of the Florida State Museum, Biological Science, No. 15(4)
  29. Miller, L. H. 1911. Avifauna of the Pleistocene cave deposits of California. University of California Bulletin, Department of Geology 6:385-400.
  30. Olson, S. L. 1984. A very large enigmatic owl from the late Pleistocene at Ladds, Georgia. Special Publication, Carnegie Museum of Natural History, 8:44-46.
  31. a b «Bird Master Database Search- Bubo virginianus». Florida Museum of Natural History. Consultado em 23 de Setembro de 2019
  32. a b Stiles, F. G. and A. F. Skutch. 1989. A guide to the birds of Costa Rica. Comstock Publishing Associates, Cornell University Press, Ithaca, NY.
  33. a b c Traylor, M. A. (1958). Variation in South American Great Horned Owls. The Auk, 143-149.
  34. a b c d Holt, D. W., Berkley, R., Deppe, C., Enríquez Rocha, P. L., Olsen, P. D., Petersen, J. L., & Wood, K. L. (1999). 69. Great Horned Owl. Handbook of Birds of the World, 5.
  35. Dickerman, R. W. 1991. On the validity of Bubo virginianus occidentalis (Stone). Auk 108:964-965.
  36. Browning, M. R. and R. C. Banks. 1990. The identity of Pennant's "Wapacuthu Owl" and the subspecific name of the population of Bubo virginianus from west of Hudson Bay. Journal of Raptor Research, 24:80-83.
  37. Dickerman, R. W. 1993. The subspecies of the Great Horned Owls of the central great plains, with notes on adjacent areas. Kansas Ornithology Society Bulletin, 44:17-21.
  38. a b c d Taverner, P. A. (1942). Canadian Races of the Great Horned Owls. The Auk, 234-245.
  39. Bendire, Charles (1892). Smithsonian Contributions to Knowledge: Life Histories of North American Birds. [S.l.]: The Smithsonian Institution. p. 383. Consultado em 9 de fevereiro de 2012
  40. Godfrey, W. E. 1986. The birds of Canada. Revised. National Museum of Natural Sciences, Ottawa.
  41. Snyder, L. L. 1961. On an unnamed population of the Great Horned Owl. Ontario Museum, Contribution 54.
  42. Dickerman, R. W., & Johnson, A. B. (2008). Notes on Great Horned Owls nesting in the Rocky Mountains, with a description of a new subspecies. Journal of Raptor Research, 42(1), 20-28.
  43. Howell, S. N. G. and S. Webb. 1995. A guide to the birds of Mexico and northern Central America. Oxford Univ. Press, New York.
  44. Ridgely, R. S. and J. A. Gwynne, Jr. 1989. A guide to the birds of Panama. Second edition. Princeton Univ. Press, Princeton, NJ.
  45. Flack, J.A.O. 1976. Bird populations of aspen forests in Western North America. Ornithological Monograph 19: 1-97.
  46. Mcgarigal, K. and J. D. Fraser. 1984. The effect of forest stand age on owl distribution in southwestern Virginia. Journal of Wildlife Management, 48:1393-1398.
  47. James, D. A. and J. C. Neal. 1986. Arkansas birds: their distribution and abundance. University of Arkansas Press, Fayetteville.
  48. Morrell, T. E. and R. H. Yahner. 1994. Habitat characteristics of Great Horned Owls in southcentral Pennsylvania. Journal of Raptor Research, 28:164-170.
  49. Smith, D. G. and J. R. Murphy. 1982. Nest site selection in raptor communities of the Eastern Great Basin Desert. Great Basin Naturalist, 42:395-404.
  50. Root, T. 1988. Atlas of wintering North American birds: an analysis of Christmas bird count data. University of Chicago Press, Chicago.
  51. Fjeldså, J. and N. Krabbe. 1990. Birds of the high Andes. Zoological Museum, University of Copenhagen, and Apollo Books, Svendborg, Denmark.
  52. Accordi, I. A., & Barcellos, A. (2006). Composição da avifauna em oito áreas úmidas da Bacia Hidrográfica do Lago Guaíba, Rio Grande do Sul. Revista Brasileira de Ornitologia, 14(2), 101-115.
  53. Johnson, D. H. 1993. Spotted Owls, Great Horned Owls, and forest fragmentation in the Central Oregon Cascades. Master's Thesis. Oregon State University, Corvallis.
  54. Rohner, C. and C. J. Krebs. 1996. Owl predation on snowshoe hares: consequences of antipredator behaviour. Oecologia 198:303-310.
  55. Ganey, J. L., & Vojta, S. C. (2005). Changes in snag populations in northern Arizona mixed-conifer and ponderosa pine forests, 1997–2002. Forest science, 51(5), 396-405.
  56. a b Errington, P.L. 1932. Studies on the Behavior of the Great Horned Owl. Wilson Bulletin, 12: 212-220.
  57. a b Baerg, W. J. (1926). Trying to Tame a Great Horned Owl. The Auk, 214-217.
  58. Austing, G.R. & Holt, Jr., J.B. (1966). The World of the Great Horned Owl. Lippingcott Company, Philadelphia (3ª impressão)
  59. Hume, R. (1991). Owls of the world. Running Press, Philadelphia, PA. 1991.
  60. a b c d e f Rohner, C. 1996. The numerical response of Great Horned Owls to the snowshoe hare cycle: consequences of non-territorial 'floaters' on demography. Journal of Animal Ecology, 65:359-370.
  61. «Stacey O'Brien : Wesley the Owl: Crows and Ravens: The Corvids and their odd behavior». 13 de abril de 2010
  62. Baumgartner, F. M. 1939. Territory and population in the Great Horned Owl. Auk 56:274-282.
  63. Millard, J. B., T. H. Craig, and O. D. Markham. 1978. Cannibalism by an adult Great Horned Owl. Wilson Bulletin, 90:449.
  64. Houston, C. S. 1978. Recoveries of Saskatchewan-banded Great Horned Owls. Canadian Field-Naturalist, 92:61-66.
  65. Smith, D. G. and J. R. Murphy. 1973. Breeding ecology of raptors in the eastern Great Basin of Utah. Brigham Young University Science Bulletin Biological Services, 18(3):1-76.
  66. Fuller, M. R. 1979. Spatiotemporal ecology of four sympatric raptor species. Ph.D. thesis. Univ. of Minnesota, St. Paul.
  67. Packard, R. L. (1954). Great horned owl attacking squirrel nests. The Wilson Bulletin, 272-272.
  68. Vaughan, T.A. 1954. Diurnal foraging by the Great Horned Owl. Wilson Bulletin 66: 148.
  69. Petersen, L. 1979. Ecology of Great Horned Owls and Red-tailed Hawks in southeastern Wisconsin. Wisconsin Department of Natural Resources Technical Bulletin, 111.
  70. Rudolph, S. G. (1978). Predation Ecology of Coexistng Great Horned and Barn Owls. The Wilson Bulletin, 134-137.
  71. Smith, D. G. and B. A. Smith. 1972. Hunting methods and success of newly-fledged Great Horned Owls. Bird-Banding 43:142.
  72. a b c Errington, P. L., F. Hamerstrom, and F. N. Hamerstrom, Jr. 1940. The Great Horned Owl and its prey in north-central United States. Iowa Agricultural Express Research Bulletin, 277:757-850.
  73. Orians, G., & Kuhlman, F. (1956). Red-tailed hawk and horned owl populations in Wisconsin. Condor, 371-385.
  74. Einarsen, A. S. 1956. Determination of some predator species by food signs. Oregon State Monographs, 10: 34.
  75. Longland, W. S. and M. V. Price. 1991. Direct observations of owls and heteromyid rodents: can predation risk explain microhabitat use? Ecology 72:2261-2273.
  76. a b c Cromrich, L. A., Holt, D. W., & Leasure, S. M. (2002). Trophic niche of North American great horned owls. Journal of Raptor Research, 36(1), 58-65.
  77. Murphy, R. K. (1997). Importance of prairie wetlands and avian prey to breeding Great Horned Owls (Bubo virginianus) in northwestern North Dakota. United States Department of Agricultural, Forest Service General Technical report, 286-298.
  78. Jaksić, F. M., & Marti, C. D. (1984). Comparative food habits of Bubo owls in Mediterranean-type ecosystems. Condor, 288-296.
  79. a b c Smith, Dwight G. (2002). Great Horned Owl 1ª ed. Mechanicsburg, PA: Stackpole Books. pp. 33; 80–81. ISBN 978-0811726894. Consultado em 21 de março de 2013
  80. «These Owl Chicks Have Two Moms and a Dad—a First». 2 de maio de 2018
  81. a b c d e f g h i j Baumgartner, F. M. (1938). Courtship and nesting of the great horned owls. The Wilson Bulletin, 274-285.
  82. Morse, Douglass H. (Abril de 1971). «Great Horned Owls and Nesting Seabirds». The Auk. 88 (2). pp. 426–427. ISSN 0004-8038. JSTOR 4083889. doi:10.2307/4083889
  83. WALEED (29 de agosto de 2018). «Great Horned Owl Nest – Interesting Facts & Information». Great Horned Owl (em inglês). Consultado em 21 de fevereiro de 2020
  84. Mader, W. J. 1973. Notes on nesting Great Horned Owls in southern Arizona. Raptor Research, 7:109-111.
  85. Bendire, C. E. 1892. Life histories of North American birds with special reference to their breeding habits and eggs. Smithsonian Contributions to Knowledge 28:376-389.
  86. Burkholder, G. & Smith, D.G. 1988. Great Horned Owl (Bubo virginianus) nesting in a Great Blue Heron (Ardea herodias) heronry. Journal of Raptor Research, 22 (2): 62.
  87. Smith, D. G. 1969. Nesting ecology of the Great Horned Owl, Bubo virginianus. Brigham Young University Science Bulletin Biological Services, 10(4):16-25.
  88. Austing, G. R. 1968. The owls and I. Audubon 70:72-79.
  89. Peck, G. K. and R. D. James. 1983. Breeding birds of Ontario: nidiology and distribution. Vol. 1. Royal Ontario Museum, Toronto.
  90. a b Turner, Jr., J. C. and L. McClanahan, Jr. 1981. Physiogenesis of endothermy and its relation to growth in the Great Horned Owl, Bubo virginianus. Compilation of Biochemical Physiology, 68A:167-173.
  91. a b Hoffmeister, D. F. and H. W. Setzer. 1947. The postnatal development of two broods of Great Horned Owls (Bubo virginianus). University of Kansas Publishing Museum of Natural History, 1:157-173.
  92. Sumner, Jr., E. L. 1934. The behavior of some young raptorial birds. University of California, Publication on Zoology, 40:331-362.
  93. Mcinvaille, Jr., W. B. and L. B. Keith. 1974. Predator-prey relations and breeding biology of the Great Horned Owl and Red-tailed Hawk in central Alberta. Canadian Field-Naturalist, 88:1-20.
  94. Dunstan, T. C. 1970. Post-fledging activities of juvenile Great Horned Owls as determined by radio-telemetry. Ph.D. thesis. University of South Dakota, Vermillion.
  95. Fuller, M. R. 1979. Spatiotemporal ecology of four sympatric raptor species. Ph.D. thesis. University of Minnesota, St. Paul.
  96. Houston, C.S. 1971. Brood size of Great Horned Owls in Saskachetwan. Bird-Banding, 42:103-105.
  97. Weller, M. W. 1965. Bursa regression, gonad cycle and molt of the Great Horned Owl. Bird-Banding 36:102-112.
  98. «Great Horned Owl (Bubo virginianus)». Alberta Environment & Parks

Leitura adicional

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Corujão-orelhudo: Brief Summary ( португалски )

добавил wikipedia PT

A jacurutu (Bubo virginianus), também conhecida como corujão-orelhudo, jucurutu, mocho-orelhudo ou corujão-da-virgínia, é uma coruja de grande porte nativa das Américas. É uma ave extremamente adaptável com uma vasta distribuição, sendo a mais amplamente distribuída do continente. Sua alimentação consiste em coelhos e lebres e ratos, apesar de caçar livremente qualquer animal que consiga, incluindo roedores e outros pequenos mamíferos, mamíferos de médio porte, aves, répteis, anfíbios e invertebrados. Em estudos ornitológicos, a jacurutu é frequentemente comparada ao bufo-real (Bubo bubo), uma espécie proximamente aparentada, que, apesar do tamanho notavelmente maior, ocupa o mesmo nicho ecológico na Eurásia, e ao búteo-de-cauda-vermelha (Buteo jamaicensis), com o qual frequentemente compartilha habitat, presas e hábitos de nidificação similares, sendo assim um equivalente ecológico durante o dia. É uma das primeiras espécies a nidificar na América do Norte, pondo seus ovos semanas ou até meses antes de outras aves de rapina.

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Výr bielobradý ( словачки )

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Výr bielobradý alebo výr západný, výr virgínsky (lat. Bubo virginianus) je najväčšia a zrejme aj najsilnejšia americká sova vyskytuje sa v Severnej, Strednej a Južnej Ameriky – od severnej hranice rozšírenia lesa až po Patagóniu.

Opis

Výr bielobradý meria v dĺžke 51 – 60 cm a váži 900 – 1 500 g. Výr bielobradý má hrdzavohnedé očné disky a čierny zobák, žltočierne perové ušká a svetlohnedé líca, perie okolo zobáka je šedé. Pod zobákom na mieste brady má biele perie a na hrudi má tmavohnedé škvrny na bielom perí. Na bielom chvoste je päť čiernych pruhov a nohy má bielej farby. Má rozpätie krídel 101 – 153 cm. Hlava meria 20 cm. Výr, ako všetky ostatné sovy, má dobrý ostrý zrak. Na nohách má 4 pazúre. Na lebke má výr bielobradý dve veľké očné jamky a veľký zobák. Kostra dolných končatín a kostra krídel sú väčšie. Výr bielobradý, ako aj niektoré iné sovy, má výrazné perové ušká. Ich presný význam nie je známy. Podľa niektorých odborníkov slúžia na „rozbitie“ tvaru sovy – čiže na jeho maskovanie. Podľa iných sú určené na vnútrodruhovú komunikáciu a druhové rozpoznávanie. Faktom je, že perové ušká nijako nesúvisia so sluchom.

Spôsob života

Výr bielobradý nie je špecializovaný na hniezdisko. Hniezdi na skalných stenách a na starých budovách s úkrytmi. Živí sa menšími cicavcami, obojživelníkmi, plazmi (mladými aligátormi severoamerickými), rybami a kôrovcami. Je aktívny najmä v noci. Samica nakladie 1 – 5 vajec o ktoré sa starajú obidvaja rodičia. Rodičia sa starajú o mláďa ešte aj 6 týždňov po tom, čo mláďa opustí hniezdo. Mláďa má funkčné perie už od dvoch mesiacov. Rodičia si potomstvo srdnato bránia – sú známe prípady, keď účinne zabránili prístupu k mláďatám aj človeku.

Iné projekty

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Výr bielobradý: Brief Summary ( словачки )

добавил wikipedia SK

Výr bielobradý alebo výr západný, výr virgínsky (lat. Bubo virginianus) je najväčšia a zrejme aj najsilnejšia americká sova vyskytuje sa v Severnej, Strednej a Južnej Ameriky – od severnej hranice rozšírenia lesa až po Patagóniu.

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Virginiauv ( шведски )

добавил wikipedia SV

Virginiauv[2] (Bubo virginianus) är en amerikansk uggla som tillhör släktet Bubo.[3] Den är nästan lika stor som berguven. Arten är aldrig sedd i västra palearktis. Möjligen kan parkrymlingar förekomma.

Utseende

Virginiauven är en stor fågel, med en längd på mellan 46 och 63 centimeter (honan är störst) och en vingspann mellan 101 och 145 centimeter. Vikten ligger mellan 0,9 och 2,5 kilogram.[4] Den har stora örontofsar, gula ögon och en fjäderdräkt som är spräcklig i brunt, grått och svart upptill med vit strupfläck; buken är ljusare med bruna tvärstreck.[5]

Ekologi

Biotop

Den finns i många miljöer, från skogar, öknar och även bebodda områden. Den tenderar dock att föredra öppen terräng som ängar och odlade fält.[4]

Föda

Virginiauven, som jagar på natten, tar ett flertal byten, framför allt mindre däggdjur (det är en av de få djur som tar skunkar) och fåglar (även rovlevande fåglar som andra ugglor, pilgrimsfalk och fiskgjusar), men även reptiler, groddjur och ryggradslösa djur.[4]

Häckning

Den bygger inget eget bo, utan föredrar att ta över andra fåglars reden. Den är inte särskilt noga med placeringen; boet kan finnas i träd, klippskrevor, ihåliga träd, byggnader eller på marken.[4] Honan lägger en till fem vita, nästan klotrunda ägg[4], som ruvas i mellan 4 och 5 veckor. Ungarna blir flygga efter fem veckor.[5]

Utbredning och systematik

Virginiauven förekommer i Nordamerika, Centralamerika och norra Sydamerika. Den delas in i hela 14 underarter med följande utbredning.[3]

  • B. v. algistus – västra Alaska
  • B. v. lagophonus – centrala Alaska till nordöstra Oregon, Idaho och nordvästra Montana
  • B. v. saturatus – kustnära sydöstra Alaska till kustnära norra Kalifornien
  • B. v. pacificus – kustnära centrala Kalifornien till nordvästra Baja California
  • B. v. subarcticus – västcentrala Kanada till norra Idaho
  • B. v. pallescens – sydvästra USA till södra Mexiko
  • B. v. pinorum – södra Idaho till norra Arizona och norra New Mexico
  • B. v. heterocnemis – nordöstra Kanada till området kring Stora Sjöarna
  • B. v. virginianus – sydöstra Kanada till centrala och östra USA
  • B. v. elachistus – södra Baja California
  • B. v. mayensisYucatánhalvön
  • B. v. mesembrinus – södra Mexiko till västra Panama
  • B. v. nigrescensColombia till nordvästra Peru
  • B. v. nacurutu – östra Colombia genom Guyanaregionen till nordöstra Brasilien, Argentina, Bolivia och centrala Peru

Magellanuven (B. magellanicus) behandlas ofta som underart till virginiauven.[6]

Status

Enligt IUCN är den inte hotad (livskraftig, LC)[1]. Den är emellertid själv en fara för hotade arter som pilgrimsfalk[4].

Noter

  1. ^ [a b] BirdLife International 2012 Bubo virginianus Från: IUCN 2013. IUCN Red List of Threatened Species. Version 2013.1 www.iucnredlist.org. Läst 6 januari 2014.
  2. ^ Sveriges ornitologiska förening (2017) Officiella listan över svenska namn på världens fågelarter, läst 2017-08-14
  3. ^ [a b] Gill, F & D Donsker (Eds). 2016. IOC World Bird List (v 6.3). doi : 10.14344/IOC.ML.6.3.
  4. ^ [a b c d e f] ”Great Horned Owl” (på en). The Cornell Lab of Ornithology, Cornell University. 2009. http://www.allaboutbirds.org/guide/Great_Horned_Owl/lifehistory. Läst 31 maj 2009.
  5. ^ [a b] Gregory Gough. ”Great Horned Owl” (på en). USGS Patuxent Wildlife Research Center. http://www.mbr-pwrc.usgs.gov/id/framlst/i3750id.html. Läst 31 maj 2009.
  6. ^ Clements, J. F., T. S. Schulenberg, M. J. Iliff, D. Roberson, T. A. Fredericks, B. L. Sullivan, and C. L. Wood (2016) The eBird/Clements checklist of birds of the world: Version 2016 http://www.birds.cornell.edu/clementschecklist/download, läst 2016-08-11
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Virginiauv: Brief Summary ( шведски )

добавил wikipedia SV

Virginiauv (Bubo virginianus) är en amerikansk uggla som tillhör släktet Bubo. Den är nästan lika stor som berguven. Arten är aldrig sedd i västra palearktis. Möjligen kan parkrymlingar förekomma.

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Amerika puhusu ( турски )

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Amerika puhusu (Bubo virginianus), baykuşgiller (Strigidae) familyasından, Kuzey Amerika'da yaşayan puhu cinsinden iri bir baykuş türü.

Özellikler

43–64 cm uzunluğunda, 91–153 cm kanat genişliğindedir[1][2][3][4]. Dişiler erkeklerden daha büyüktür. Ortalama olarak bir yetişkin 52 cm uzunluğa, 124 cm kanat genişliğine ve 1.4 kg ağırlığa sahiptir[5].

Beslenme

Çoğunlukla, tavşan gibi ortaboy ya da fare, sincap, lemming gibi küçük memelilerle beslenirler[3][4]. Düzenli olarak yediği diğer memliler arasında sivri fare, yarasa, tatu, misk sıçanı, sansar ve gelincik bulunur[3][4].

Kaynakça

  1. ^ Bubo virginianus profile
  2. ^ Profile
  3. ^ a b c Owls of the World by Konig, Weick & Becking. Yale University Press (2009), ISBN 0300142277
  4. ^ a b c "Great Horned Owl – Bubo virginianus – Information, Pictures, Sounds". Owlpages.com. 1 Aralık 2015 tarihinde kaynağından arşivlendi. Erişim tarihi: 2012-02-09.
  5. ^ University of Michigan Profile
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Amerika puhusu: Brief Summary ( турски )

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Amerika puhusu (Bubo virginianus), baykuşgiller (Strigidae) familyasından, Kuzey Amerika'da yaşayan puhu cinsinden iri bir baykuş türü.

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Пугач віргінський ( украински )

добавил wikipedia UK
  1. Фесенко Г. В. Вітчизняна номенклатура птахів світу. — Кривий Ріг : ДІОНАТ, 2018. — 580 с. — ISBN 978-617-7553-34-1.
  2. Про сов на сайті "Проеко"
  3. Інформація про сов на сайті "Укрзоо"
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Cú sừng ( виетнамски )

добавил wikipedia VI

Cú sừng, tên khoa học Bubo virginianus, là một loài chim trong họ Strigidae.[2]

Phân loài

Nhiều phân loài của loài này đã được đặt tên, chúng khác nhau chủ yếu về màu sắc và kích thước và nhìn chung chúng tuân theo quy tắc của GlogerBergmann:[3]

  • Bubo virginianus virginianus (Gmelin, 1788)
  • Bubo virginianus nacurutu (Vieillot, 1817)[4]
  • Bubo virginianus subarcticus (Hoy, 1852)[5][6]
  • Bubo virginianus pacificus (Cassin, 1854)
  • Bubo virginianus saturatus (Ridgway, 1877)
  • Bubo virginianus nigrescens (Berlepsch, 1884)
  • Bubo virginianus pallescens (Stone, 1897)
  • Bubo virginianus mayensis (Nelson, 1901)

Hình ảnh

Chú thích

  1. ^ BirdLife International (2012). Bubo virginianus. Sách Đỏ IUCN các loài bị đe dọa. Phiên bản 2013.2. Liên minh Bảo tồn Thiên nhiên Quốc tế. Truy cập ngày 26 tháng 11 năm 2013.
  2. ^ Clements, J. F., T. S. Schulenberg, M. J. Iliff, B.L. Sullivan, C. L. Wood, and D. Roberson (2012). “The eBird/Clements checklist of birds of the world: Version 6.7.”. Truy cập ngày 19 tháng 12 năm 2012.
  3. ^ Houston et al. (1998), Holt et al. (1999)
  4. ^ Holt et al. (1999)
  5. ^ Holt et al. (1999), Dickerman (2002, 2004).
  6. ^ Smithsonian contributions to knowledge – Smithsonian Institution – Google Books. Books.google.com. Ngày 5 tháng 11 năm 2009. Truy cập ngày 9 tháng 2 năm 2012.

Tham khảo


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Cú sừng: Brief Summary ( виетнамски )

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Cú sừng, tên khoa học Bubo virginianus, là một loài chim trong họ Strigidae.

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Виргинский филин ( руски )

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Царство: Животные
Подцарство: Эуметазои
Без ранга: Вторичноротые
Подтип: Позвоночные
Инфратип: Челюстноротые
Надкласс: Четвероногие
Класс: Птицы
Подкласс: Настоящие птицы
Инфракласс: Новонёбные
Семейство: Совиные
Подсемейство: Настоящие совы
Род: Филины
Вид: Виргинский филин
Международное научное название

Bubo virginianus (Gmelin, 1788)

Ареал

изображение

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Систематика
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ITIS 177884NCBI 56268EOL 914958FW 161527

Вирги́нский фи́лин[1] (Bubo virginianus) — хищник из семейства совиных или настоящих сов, широко распространён на территориях обеих Америк. Встречается как в лесах, так и в степях и пустынных зонах. Является самым крупным представителем сов в Новом Свете и вторым по счёту в мире в целом (после филина евроазиатского).

Описание

Впервые был замечен на территории колонии Виргиния, по имени которой и был назван. Окраска у него преимущественно от рыжевато-бурой до серой, чёрной или белой. Размах его крыльев достигает 1,5 метров. У птиц, живущих в тундре и пустыне, преобладает более светлый окрас, а у тех, кто живёт в лесах, — более тёмный. На голове у него есть перьевые «ушки», за что его прозвали «большим рогатым филином». Снизу у него окрас перьев более светлый, с темными разводами и пересекающими белыми полосами.

У филинов большие оранжево-жёлтые глаза. У некоторых видов имеется пуховая кайма, обрамляющая лицевую часть головы. Молодые особи по внешнему виду похожи на взрослых. Самки в среднем крупнее самцов на 10—20 %. Длина тела взрослой птицы около 46—63,5 см, а размах крыльев 91—152 см. Масса взрослых особей от 900 до 1800 грамм.

Виргинские филины издают глухие гудящие звуки, также они могут издавать громкие визги, урчание и короткие звуки, похожие на звуки кашля.

Распространение

Виргинский филин распространён практически по всей территории Северной Америки, за исключением Крайнего Севера. Встретить его можно практически везде: в лесах, степях, пустынях и сельскохозяйственных землях. Встречается и в городских парках. Является оседлым, но птицы северных территорий могут откочёвывать к югу зимой. В Южной Америке встречается в предгорьях Анд и в зоне редколесий, а также в некоторых других местах. Ареал не выходит за пределы Америки.

Гнездится в дуплах или брошенных гнёздах других птиц. Может гнездиться в домах, расселинах скал и даже пещерах. Иногда гнездится на земле.

Поведение

Виргинские филины преимущественно ведут ночной образ жизни и активны ночью. Зимой ведут одиночный образ жизни, летом же собираются в пары. Члены семьи филинов держатся вместе до осени, после чего молодняк улетает. Предпочитают одиночный образ жизни, собираясь в пары в период размножения.

Размножение

Брачный период начинается в январе-феврале. Во время брачного периода самцы активно призывают пением самок, которые иногда присоединяются к пению. Филины очень агрессивны при защите гнезда и атакуют врага, пока не убьют или не изгонят его. Самка откладывает 2—4 яйца с промежутком в два-три дня в апреле-мае. Насиживание яиц осуществляется только самкой и обычно длится около 32 суток. Птенцы филина начинают покидать гнездо на 5—7 неделе, способности к полёту приобретают к 9—10 неделе. Растут преимущественно медленно. Выкармливание птенцов длится несколько недель.

Питание

Виргинские филины предпочитают охоту из засады и атакуя с воздуха. Рацион филинов богат и включает около 253 видов животных и птиц, однако отдаёт предпочтение грызунам. За раз способен унести добычу в 2—3 раза превосходящую свой собственный вес. Нападает на птичники, воруя цыплят. Мелкую добычу глотает целиком, более же крупную расчленяет. Известно, что это единственный хищник, который способен на охоту за скунсовыми.

Интересные факты

  • Своё название филин получил от штата Вирджиния, где был впервые встречен.
  • В мультфильме Легенды Ночных стражей кузнец дерева Га’Хуула Бубо и есть Виргинский филин.
  • Из-за перьевых ушек, расположенных на голове, Виргинский филин получил прозвище «Большой рогатый филин».
  • По всей видимости, именно эту птицу («большая ушастая сова») описал Фарли Моуэт в своей книге «Собака, которая не хотела быть просто собакой». Исходя из описания, птица может быть приручена[источник не указан 2487 дней].

Фотографии

  •  src=

    Виргинский филин крупным планом

  •  src=

    Филин на ветке

  •  src=

    Филин в дупле

Примечания

  1. Бёме Р. Л., Флинт В. Е. Пятиязычный словарь названий животных. Птицы. Латинский, русский, английский, немецкий, французский / Под общ. ред. акад. В. Е. Соколова. — М.: Рус. яз., «РУССО», 1994. — С. 140. — 2030 экз.ISBN 5-200-00643-0.
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Виргинский филин: Brief Summary ( руски )

добавил wikipedia русскую Википедию

Вирги́нский фи́лин (Bubo virginianus) — хищник из семейства совиных или настоящих сов, широко распространён на территориях обеих Америк. Встречается как в лесах, так и в степях и пустынных зонах. Является самым крупным представителем сов в Новом Свете и вторым по счёту в мире в целом (после филина евроазиатского).

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大鵰鴞 ( кинески )

добавил wikipedia 中文维基百科
二名法 Bubo virginianus
(Gmelin, 1788) 分布
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亞種
  • 參見內文

大雕鴞學名Bubo virginianus)是美洲一種大型的貓頭鷹。牠們的適應力強,是美洲分佈得最廣的鴟鴞科

南美洲南部的小雕鴞經常被認為是大雕鴞的亞種

特徵

大雕鴞長46-68厘米,翼展長101-153厘米。雌鳥比雄鳥大,平均長55厘米,翼展長124厘米,重1.4公斤。較大的個體分佈在近極地,較小的個體則接近赤道,符合伯格曼定律(Bergmann's Rule)。

 src=
B. v. virginianus的面部。

大雕鴞的耳邊絨毛很大,面部呈紅色、褐色或灰色,喉嚨有一片白色。虹膜黃色,其下B. V. nacurutu的虹膜則是琥珀色。其「角」並非耳朵或是真正的角,而只是絨毛或羽毛。下身淺色帶有褐色斑紋。腳上至爪前都長有羽毛。個別及地區性的顏色都有分別:靠近極地的個體呈較淺色,而在中美洲的則呈深朱古力褐色。

大雕鴞的叫聲是低音但大部的咕咕聲,一連四或五個音節。雌鳥的叫聲較高音,尾音上升。幼鳥只會發出嘶嘶聲,很易與倉鴞的叫聲混淆。

大雕鴞很易與小雕鴞及其他雕鴞屬混淆。不過牠們一般都是異域的。

亞種

大雕鴞之下命名了很多亞種,但是其中很多都是一些個體或漸變群。亞種的分別主要是在毛色及大小,而且一般都符合格洛格尔律伯格曼定律[2][3]

 src=
B. v. nacurutu
  • B. v. nacurutu:棲息在低地的形態,散佈在哥倫比亞東部至圭亞那玻利維亞巴西南部的亞馬遜盆地阿根廷北部。牠們全年是留鳥。這個亞種中亦有一些建議的亞種,包括B. v. scotinusB. v. elutusB. v. deserti[3]牠們呈深褐色,喙很長。在巴西半乾旱內陸群落的上尾及耳底有較多的白色。牠們是唯一擁有琥珀虹膜的亞種。
  • B. v. subarcticus繁殖分佈地在英屬哥倫比亞馬更些(Mackenzie)東至哈德遜灣;南端邊界不詳,但最少會至蒙大拿州北達科他州,。非繁殖的一般會在南至南緯45°的地方出沒,有時會南下得更遠。其下包括被命名為B. v. occidentalisB. v. sclariventris[4]舊有的名稱B. v. wapacuthu有時也會用作稱呼這個亞種,但卻只能作為一個可疑名。B. v. algistus的群落可能只是一些走失的個體,或是B. v. subarcticusB. v. saturatusB. v. lagophonus的過渡體。[3]這是較為淡色的亞種,上身呈白色至淺黃色,下身有黑色斑紋。非常淡色的個體則會很像雌性的雪鴞。腳呈白色至淺黃色,有很少或沒有斑紋。
 src=
正在伸展的B. v. pacificus
  • B. v. saturatus:分佈在阿拉斯加東南部至加利福尼亞州北部的太平洋海岸。全年均是留鳥。牠們呈深沉灰色,下身有很多斑紋。腳呈暗色。
  • B. v. pallescens:分佈在聖華金谷(San Joaquin Valley)向東南經加利福尼亞州東南部及猶他州南部,東至堪薩斯州西部及南至墨西哥格雷羅州韋拉克魯斯州西部。牠們與B. v. pacificus的過渡體分佈在聖地牙哥郡。B. v. lagophonus洛磯山脈群落也在其分佈地出沒。全年也是留鳥。牠們細小及呈淡淺黃色,有不明顯的斑紋。肱骨部份呈棕土色,腳半白色及沒有斑紋。
  • B. v. mayensis:分佈在猶加敦半島,全年留鳥。牠們的體型細小至中等,淡色。
  • B. v. elachistus:分佈在下加利福尼亞州南部,全年留鳥。牠們的毛色像B. v. pacificus,但稍為細小。
  • B. v. heterocnemis:繁殖分佈地在加拿大東部。於冬天會向南的安大略省及美國東北部遷徙。很難與B. v. saturatus分辨。[3]

牠們呈深灰色,有很多斑紋。腳呈淡色及狼斑紋。

  • B. v. lagophonus:繁殖分佈地在阿拉斯加內陸經英屬哥倫比亞的山區至俄勒岡州斯內克河及蒙大拿州西北部。冬天向南遷徙至科羅拉多州及德克薩斯州。很難與B. v. saturatus分辨。[3]牠們比B. v. saturatus較為灰色,但整體相似。腳有暗色的斑紋。
  • B. v. mesembrinus:分佈在特旺特佩克地峽(Isthmus of Tehuantepec)至巴拿馬西部,全年留鳥。牠們呈中等身型,比B. v. mayensis較為深色。
  • B. v. ssp. nov.:洛磯山脈群落,可能是一個未描述的亞種。牠們的繁殖分佈地在斯內特河南部南至亞利桑那州新墨西哥州瓜達洛普山(Guadalupe Mountains),西至Modoc高原及莫諾湖(Mono Lake)。B. v. occidentalis可能是牠們的名稱,也有被認為是B. v. pallescensB. v. lagophonus的過渡體。[3]牠們呈中灰色,介乎B. v. lagophonusB. v. pallescens兩色之間。下身有淡黃色的陰影及略略有斑紋。腳也有斑紋。

加利福尼亞州發現的古新世Bubo sinclairi可能是大雕鴞的古亞種[5]

分佈及生態

大雕鴞的影片。

大雕鴞分佈在北美洲亞北區中美洲南美洲南至火地群島。在瓜地馬拉南部、薩爾瓦多尼加拉瓜巴哈馬亞馬遜森林及南美洲南部、與及西印度群島及大部份海島上都不會見到大雕鴞。[3][6]

大雕鴞會棲息在樹上,包括落葉林、針葉林混交林熱帶雨林潘帕平原大草原區、沙漠、亞北區的凍土層、石灘、紅樹林及一些市區。牠們較少出沒在極端氣候的地區,並不會到濕地環境[7]及高海拔的凍土層。所有已交配的大雕鴞都是留鳥,未交配的或幼鳥就會在較少食物供應的冬天離開,到處尋找伴侶及地盤。

大雕鴞的鳥蛋及雛鳥是狐狸郊狼野貓的獵物。成鳥並沒有天敵,但與雪鴞及其他大雕鴞對抗時可能會被殺死。牠們並非受到威脅的生物。[1]

食物及行為

 src=
大雕鴞飛行時的重疊圖。

大雕鴞有雙目視覺,可以準確尋找獵物及在低光度下仍能看見。牠們的眼睛大如人類的,但卻不能在眼窩內轉動。所以大雕鴞會轉動頭部。其頸部在身體保持不動時可以轉動達270°。

大雕鴞的聽覺也很好。牠們感覺深度的能力比人類更強。這是由於牠們的耳朵並非在頭的兩側,而是在頭較高的位置。只要傾斜或轉動頭部,牠們就可以準確測量聲音的橫向及直向位置。

大雕鴞是在夜間獵食,會站在高處等待獵物,再俯衝擒獲獵物。牠們主要狩獵細小至中等的哺乳動物,如野兔浣熊大家鼠松鼠小鼠屬鼴科田鼠旱獺鼩鼱科蝙蝠犰狳科鼬屬沙鼠。牠們更是豪豬鼬鼠的天敵。牠們也會獵食其他鳥類,由細小的戴菊鳥至大如大藍鷺不等。涉禽(尤其是蹼雞屬),甚至乎猛禽雪鴞都會被獵食。牠們有時會吃農場的。牠們卻只會有時吃爬行類兩棲類魚類甲殼類昆蟲。也有紀錄牠們會同類相食

大雕鴞爪的壓力可以達到每平方吋500磅,遠遠超過人手的60磅的握力。在北部若有較大的獵物,牠們會將吃剩的獵物冰凍起來,到有需要時再用體溫來解凍。牠們傾向在同一地方反芻食物。

繁殖

 src=
雛鳥。

大雕鴞是北美洲最早繁殖鳥類。牠們於1月下旬或2月初繁殖,在10月的冬天就開始互相呼叫。牠們會在12月前交配。位於熱帶氣候的群落,其繁殖季節很不明確。牠們會接管其他大至鳥類的鳥巢,有時更會加些羽毛烏鴉渡鴉紅尾鵟或大型松鼠的巢都是牠們的對象。牠們有時也會利用樹洞、崖壁、空置大廈及人工平台等作為鳥巢。

大雕鴞每次平均會生2隻蛋,介乎1-5隻蛋。鳥蛋平均闊4.65厘米,長5.52厘米,重51克。孵化期介乎30-37日,平均33日。雙親會不斷哺育雛鳥至兩星期大,隨後開始減少。6星期大的幼鳥會移到附近的樹枝,1星期後開始學飛。雛鳥在10月下旬仍會要求哺育及未離開雙親,直至12月雙親開始繁殖第二胎。幼鳥會有1-2年時間的交配空白期,這段時間牠們會流浪,直至牠們交配及建立自己的地盤。

象徵

大雕鴞是加拿大艾伯塔省的省鳥。

參考

  1. ^ 1.0 1.1 BirdLife International. Bubo virginianus. IUCN Red List of Threatened Species. 2014, 2014: e.T61752071A61752159. doi:10.2305/IUCN.UK.2014-2.RLTS.T61752071A61752159.en.
  2. ^ Houston, C. S., Smith, D. G. & Rohner, C. Great Horned Owl (Bubo virginianus). (编) Poole, A. & Gill, F. (eds.). Birds of North America. Academy of Natural Sciences, Philadelphia, PA & American Ornithologists' Union, Washington, D.C. 1998: 372. doi:10.2173/bna.372.
  3. ^ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Holt, Denver W.; Berkley, Regan; Deppe, Caroline; Enríquez Rocha, Paula L.; Olsen, Penny D.; Petersen, Julie L.; Rangel Salazar, José Luis; Segars, Kelley P. & Wood, Kristin L. Great Horned Owl. (编) del Hoyo, J.; Elliott, A. & Sargatal, J. (eds). Handbook of Birds of the World (Volume 5: Barn-owls to Hummingbirds). Barcelona: Lynx Edicions. 1999: 185, plate 10. ISBN 84-87334-25-3.
  4. ^ Dickerman, Robert W. Notes on the type of Bubo virginianus sclariventris (PDF). Bull. B.O.C. 2004, 124 (1): 5–6.
  5. ^ Howard, Hildegarde. A preliminary survey of trends in avian evolution from Pleistocene to recent time (PDF). Condor. 1947, 49 (1): 10–13.
  6. ^ Banks, R.C.; Cicero, C.; Dunn, J.L.; Kratter, A.W.; Ouellet, H.; Rasmussen, P.C.; Remsen, J.V. Jr.; Rising, J.A. & Stotz, D.F. Forty-second supplement to the American Ornithologists' Union Check-list of North American Birds (PDF). Auk. 2000, 117 (3): 847–58. doi:10.1642/0004-8038(2000)117[0847:FSSTTA]2.0.CO;2.
  7. ^ Accordi, Iury Almeida & Barcellos, André. Composição da avifauna em oito áreas úmidas da Bacia Hidrográfica do Lago Guaíba, Rio Grande do Sul (PDF). Revista Brasileira de Ornitologia. 2006, 14 (2): 101–15. (原始内容 (PDF)存档于2008-12-19).

外部連結

 src= 维基共享资源中相关的多媒体资源:大鵰鴞 物種識別信息  title=
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大鵰鴞: Brief Summary ( кинески )

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大雕鴞(學名:Bubo virginianus)是美洲一種大型的貓頭鷹。牠們的適應力強,是美洲分佈得最廣的鴟鴞科

南美洲南部的小雕鴞經常被認為是大雕鴞的亞種

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アメリカワシミミズク ( јапонски )

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アメリカワシミミズク Bubo virginianus (Grand-duc d'Amérique).jpg
アメリカワシミミズク Bubo virginianus
保全状況評価 LEAST CONCERN
(IUCN Red List Ver.3.1 (2001))
Status iucn3.1 LC.svg 分類 : 動物界 Animalia : 脊索動物門 Chordata 亜門 : 脊椎動物亜門 Vertebrata : 鳥綱 Aves : フクロウ目 Strigiformes : フクロウ科 Strigidae : ワシミミズク属 Bubo : アメリカワシミミズク
B. virginianus 学名 Bubo virginianus
Gmelin, 1788 和名 アメリカワシミミズク 英名 Great Horned Owl  src= ウィキメディア・コモンズには、アメリカワシミミズクに関連するメディアがあります。

アメリカワシミミズク(亜米利加鷲木莵、学名:Bubo virginianus)英名グレイトホーンアウル(大きい角のふくろう)は、フクロウ目フクロウ科に分類される鳥類の一種。

 src=
やや緊張した状態
 src=
閉眼したアメリカワシミミズク

生息地[編集]

Bubo virginianus dis.png

亜種[編集]

  • Bubo virginianus virginianus 基亜種アメリカワシミミズク
  • Bubo virginianus subarcticus
  • Bubo virginianus pallescens
  • Bubo virginianus satyratus

など

生態[編集]

森林農耕地に生息する。夜行性。タカカラスの古巣、樹洞で子育てをする。

食性は肉食性で、小型の哺乳類鳥類爬虫類両生類魚類昆虫類を捕食する。

Sibley分類体系上の位置[編集]

シブリー・アールキスト鳥類分類
鳥類 Aves

参考文献[編集]

  • ベルンド・ハインリッチ 『ブボがいた夏 アメリカワシミミズクと私』 渡辺政隆訳、平河出版社、1993年。
  • 『小学館の図鑑NEO 鳥』 小学館、2002年、158頁。
執筆の途中です この項目は、鳥類に関連した書きかけの項目です。この項目を加筆・訂正などしてくださる協力者を求めていますポータル鳥類 - PJ鳥類)。
 title=
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アメリカワシミミズク: Brief Summary ( јапонски )

добавил wikipedia 日本語

アメリカワシミミズク(亜米利加鷲木莵、学名:Bubo virginianus)英名グレイトホーンアウル(大きい角のふくろう)は、フクロウ目フクロウ科に分類される鳥類の一種。

 src= やや緊張した状態  src= 閉眼したアメリカワシミミズク
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