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Blakiston's Fish-Owl Ketupa blakistoni Scientific name definitions

Denver W. Holt, Regan Berkley, Caroline Deppe, Paula L. Enríquez, Julie L. Petersen, José Luis Rangel Salazar, Kelley P. Segars, Kristin L. Wood, Christopher J. Sharpe, and Jeffrey S. Marks
Version: 1.0 — Published March 4, 2020
Text last updated November 27, 2017

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Field Identification

60–71 cm (1); nominate: male 3150–3450 g (n = 3), female 3360–4600 g (n = 4) (2); race doerriesi: male 3100 g (mean of 7), female 3250 (mean of 5) (3); wingspan 178–190 cm (4). After Bubo bubo, the largest of all owls (5); ear tufts broad, long, typically held horizontal. Facial disc pale grey-brown; upperparts buff-brown, broadly streaked, wings barred buff and dark brown; tail almost white, barred dark; white throat; below, pale buffish-brown with long, thin streaks; tarsi feathered almost to base of toes; irides yellow; cere and bill pale grey-horn, latter yellowish at tip; toes lead-grey (1). Juvenile with spots and whitish feather edgings above; bill and toes bluish (1). Race doerriesi larger (wing length 510–560 mm versus 498–534 mm in nominate (1) ), with white crown patch.

Systematics History

Editor's Note: This article requires further editing work to merge existing content into the appropriate Subspecies sections. Please bear with us while this update takes place.

Sometimes placed in genus Ketupa, and has been thought closely related to, or even conspecific with, K. zeylonensis; skeletal details, however, especially skull morphology, appear identical to those of Bubo (e.g. B. bubo) and different from osteology of Ketupa. Proposed race piscivorus (NE China W of Great Khingan Mts) included in doerriesi, and karafutonis (Sakhalin) in nominate. Two subspecies recognized.

Subspecies


EBIRD GROUP (MONOTYPIC)

Blakiston's Fish-Owl (doerriesi) Ketupa blakistoni doerriesi Scientific name definitions

Distribution

SE Siberia and extreme ne China to Korea

EBIRD GROUP (MONOTYPIC)

Blakiston's Fish-Owl (blakistoni) Ketupa blakistoni blakistoni Scientific name definitions

Distribution

N Japan (s Kuril Islands and Hokkaido)

Distribution

Editor's Note: Additional distribution information for this taxon can be found in the 'Subspecies' article above. In the future we will develop a range-wide distribution article.

Habitat

Dense, old-growth broadleaf or mixed broadleaf/coniferous forest along clear rivers, favouring tributary confluences where some slow-flowing channels; steep-sided wooded valleys near fast-flowing rivers; also taiga rivers which do not freeze in winter; in Kurils, dense conifer forest adjacent to water, including sea coast. Also forages on rocky coasts. Lowlands. Extensive study in Primorye, Russia, revealed preference for home ranges within valleys that were close to water and had more river channels than available sites; large trees and riparian old-growth forest distinguished nest sites and foraging sites from surrounding areas; old forests had numerous large trees that provided large woody debris in rivers, which improved habitat for salmonid prey (3).

Movement

Generally considered resident, but seasonal movements poorly understood (6). Young birds may wander widely before settling on a nesting territory (7). In Russia, mean annual home range size for seven adults was 15.0 ± 3.7 km2 using the synoptic model and 38.8 ± 15.4 km2 using kernel-density estimator (3).

Diet and Foraging

Primarily fish , including large ones; also crabs, crayfish, frogs (especially in spring (6) ), and birds up to size of grouse (Tetraonidae); occasionally bats in flight. In autumn and winter, diet includes crayfish and other crustaceans as well as small mammals; sometimes cats and small dogs. Forages mainly at night (fish) or dusk (frogs); also by day. Hunts from low branch, log or bank overlooking river shallows; often walks about on ground, occasionally wades in shallow water (6); jumps on prey and kills with talons ; sometimes swoops to catch fish near surface, or dives feet first into deep water. In winter , will wait by holes in ice or snow; sometimes up to 5–6 individuals together.

Sounds and Vocal Behavior

Territorial call short, deep “boo-boo-voo”  or “shoo-hoo”; elaborate duets; begging call of young a long, slurred “peer-peer-peer” (1).

Breeding

Lays late Feb-mid Mar, when snow cover still deep. Probably pairs for life. Nest a spacious hole up to 18 m above ground in large hollow tree, or in nest box, or in fallen tree; 15 nests in Primorye ranged from 4–16·8 m above ground (3). Highly territorial, in Siberia territory covering 6–12 km of river valley, but density much higher in Primorye with 1 pair / per 3·8 km of river (6). Courtship feeding begins 4 days before first copulation; most copulations around sunset. Clutch size usually 2 eggs (1–3); egg size 55·9–69·4 mm × 49·0–52·8mm (2); incubation 35–37 days, by female, fed on nest 3–5 times nightly by male; female leaves only to defecate and preen, travelling no more than 100 m from nest; chick with white down; young leave nest at 35–40 days, remain with parents for several months; juveniles sometimes dependent on adults for up to 1 year, especially during harsh winters. Apparently breeds only in alternate years. Lifespan probably 20 years or more. Sex ratio of fledglings male-biased, with 81 males and 56 females in sample of 137 young from 91 broods (8). Several records of close inbreeding on Hokkaido, including pairings by a father and daughter, grandmother and grandson, and full siblings (albeit hatched in different years) (9).

ENDANGERED. CITES II. One of world’s rarest, and until fairly recently most poorly known owls. Numbers in Russia, including Sakhalin and S Kuril Is, estimated at 300–400 pairs in 1984, but 250–400 birds subsequently found in Primorye alone BirdLife International (2016) Species factsheet: Bubo blakistoni. Downloaded from http://www.birdlife.org on 22/07/2016. ; formerly present throughout Hokkaido (Japan), but now confined to E & C parts, where 140 individuals occur (an increase on the 80–100 birds estimated in late 1980s attributed to provision of articifial nest sites and feeding) (10), with only c. 20 pairs breeding in any year; in NE China extremely rare and local, possibly now extinct. Global population may be "a few thousand birds", and conservatively put at fewer than 2500 mature individuals BirdLife International (2016) Species factsheet: Bubo blakistoni. Downloaded from http://www.birdlife.org on 22/07/2016. . Has declined massively over entire range, especially since 1950s; on R Bikin, in Ussuriland, decrease from estimated 70 birds (26 pairs) in mid 1970s to current total of 15 pairs or fewer. Range and population now fragmented. Main threats are development of riverside habitats and deforestation, especially destruction of taiga forest in Far East and Japan; on lower R Bikin, human population pressure forcing it to move to less productive rivers. In a Russian study, 43% of optimal fish-owl habitat was within current logging leases, while protected areas included only 19% (11). Depletion of fish stocks through overfishing also an adverse factor, and water pollution is a further threat. Direct mortality often human-induced (6). This species’ habit of concentrating around fishing holes in Siberia renders it vulnerable to hunters and fishermen; also persecuted by fur-trappers, and sometimes dies in traps set for mink; hunted for food locally in Siberia. On Hokkaido, mortality has been caused by collision with powerlines and traffic as well as by drowning in nets employed on fish farms BirdLife International (2016) Species factsheet: Bubo blakistoni. Downloaded from http://www.birdlife.org on 22/07/2016. . Hokkaido population shows low genetic diversity, indicating a recent population bottleneck and fragmentation (10). Provision of nest boxes has achieved some success on Kunashiri I and Hokkaido, where pairs have bred in these artificial nests annually since 1983. Attempts at captive-breeding unsuccessful. Legally protected throughout its range BirdLife International (2016) Species factsheet: Bubo blakistoni. Downloaded from http://www.birdlife.org on 22/07/2016. . On the basis of recent research in Russia (3), management recommendations include protecting specific locations within potential territories, maintaining integrity of riparian areas, modifying road construction techniques, and closing old logging roads to reduce human access; these actions would benefit the owls as well as many other species, because the owl is an “umbrella species” for riparian ecosystems within the region (3, 12).

Distribution of the Blakiston's Fish-Owl - Range Map
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  • Year-round
  • Migration
  • Breeding
  • Non-Breeding
Distribution of the Blakiston's Fish-Owl

Recommended Citation

Holt, D. W., R. Berkley, C. Deppe, P. L. Enríquez, J. L. Petersen, J. L. Rangel Salazar, K. P. Segars, K. L. Wood, C. J. Sharpe, and J. S. Marks (2020). Blakiston's Fish-Owl (Ketupa blakistoni), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. https://doi.org/10.2173/bow.blfowl1.01
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