Sulawesi Hornbill Rhabdotorrhinus exarhatus Scientific name definitions
Text last updated December 25, 2012
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Species names in all available languages
Language | Common name |
---|---|
Catalan | calau caragroc |
Czech | zoborožec celebeský |
Dutch | Temmincks Neushoornvogel |
English | Sulawesi Hornbill |
English (United States) | Sulawesi Hornbill |
French | Calao des Célèbes |
French (France) | Calao des Célèbes |
German | Gelbmasken-Hornvogel |
Indonesian | Kangkareng sulawesi |
Japanese | カオジロサイチョウ |
Norwegian | sulawesihornfugl |
Polish | dzioborożec bruzdodzioby |
Russian | Желтолицый калао |
Serbian | Sulaveški kljunorožac |
Slovak | zobákorožec celebeský |
Spanish | Cálao Chico de Célebes |
Spanish (Spain) | Cálao chico de Célebes |
Swedish | sulawesinäshornsfågel |
Turkish | Sarı Yüzlü Boynuzgaga |
Ukrainian | Калао жовтощокий |
Rhabdotorrhinus exarhatus (Temminck, 1823)
Definitions
- RHABDOTORRHINUS
- exarhatus
The Key to Scientific Names
Legend Overview
Field Identification
45 cm; female 370 g. Small, black hornbill with green gloss on back; just two hornbills occur on Sulawesi, with Rhyticeros cassidix rather larger, a white tail, a taller casque and brightly coloured facial skin in all plumages (1). Male nominate race with white facial and throat plumage, but in life stained yellow , possibly by preen oil; bill pale yellow , black at base of lower mandible, with low, ridged casque brown; bare skin around eye and on throat dusky pinkish; eye red, legs and feet black (1). Female smaller (wing 215–231 mm versus 226–245 mm in male) (1), all-black facial skin and throat ; yellow stripe below eye (1); casque and bill blacker than in male (and casque also shorter, ending midway along bill, rather than just before tip) (1), with cream ridges across lower mandible and paler creamy tip. Juvenile like adult male, but smaller bill dull yellow, casque undeveloped, and eye dark brown (1); develops yellow facial colours from 80 days old, female acquires adult colours from c. 90–105 days. Race sanfordi differs mainly in having pale creamy yellow ridges across lower mandible , with redder-brown casque ; juvenile may possess creamy superciliary (1).
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.
Previously placed in genus Penelopides, where in the past sometimes treated as conspecific with P. panini. A recent molecular phylogeny found present species to be a member of the “wrinkled hornbill” lineage, and that its similarity to Penelopides was superficial (2). Two subspecies recognized.Subspecies
Sulawesi Hornbill (Dwarf) Rhabdotorrhinus exarhatus exarhatus Scientific name definitions
Distribution
Rhabdotorrhinus exarhatus exarhatus (Temminck, 1823)
Definitions
- RHABDOTORRHINUS
- exarhatus
The Key to Scientific Names
Legend Overview
Sulawesi Hornbill (Sanford's) Rhabdotorrhinus exarhatus sanfordi Scientific name definitions
Distribution
Rhabdotorrhinus exarhatus sanfordi Stresemann, 1932
Definitions
- RHABDOTORRHINUS
- exarhatus
- sanfordi
The Key to Scientific Names
Legend Overview
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
Lowland and lower montane primary forest, occasionally tall secondary forest, usually below 650 m but sometimes up to 1100 m; family groups sometimes in more open habitats including recently burned areas and regenerating treefall gaps (3).
Movement
Apparently sedentary and territorial.
Diet and Foraging
Diet mainly fruit (c. 85%), especially lipid-rich species (4), of at least 34 plant species and 13 families, especially Ficus spp. (Moraceae), Alstonia sumatrana (Apocynaceae), Chisocheton kingii (Meliaceae), Canarium hirsutum (Burseraceae), Polyalthia glauca (Annonaceae) and Cananga odorata (Annonaceae) (3); also some small animals, mainly invertebrates (26% or 7% of items at two nests) (3), with, in one recent study, fruit forming by far largest percentage of diet (89·4%), invertebrates constituting 9·8% and vertebrates 0·8%, while figs (Moraceae) comprised a mean c. 67% of monthly diet of the present species and Rhyticeros cassidix (4). Forages mostly through foliage below canopy, slowly and rather methodically (1). Reported to chase R. cassidix. Foraging territory when breeding 72–139 ha.
Sounds and Vocal Behavior
Considered to be generally quite noisy: gives loud piercing “kerrekerre ... kerrekerre”, with the four syllables repeated at short intervals; a staccato “clack”, similar to call of Anorrhinus galeritus; and a chicken-like cackling has also been described (1).
Breeding
Season mainly Feb–May in N Sulawei (5), prior to Rhyticeros cassidix in same region, but also reported laying in Apr and Oct. Co-operative and territorial, in noisy groups of 2–10 birds (mean four), with adult helpers of both sexes, but non-breeding females that deliver food to nest usually rejected (3). Nest on trunk or branch (5) in natural cavity or old woodpecker hole in large forest tree (mainly deciduous, more occasionally evergreen), always live, on average halfway up in tall canopy tree with a large girth (5), including sites used by R. cassidix. Cavity of 12 nests measured 27·1–107 cm (mean 61·8 cm) × 11–35 cm (25·9 cm), and entrance 11–47 cm (21·7 cm) × 5.4–21 cm (13·8 cm) (5). Nesting density of 0·75–4·2 nests/km2 (5). Usually two dirty white (1) eggs (size 47·3 mm × 34·8 mm) (1) or chicks reported in wild, and nesting cycle 70–90 days (3); in captivity, four eggs, first laid nine days after sealing in, rest at two-day intervals, with incubation 28–30 days (reported as 16–19 days in wild) (3) and fledging c. 50–60 days (55–70 in wild), with most food delivered in early morning and afternoon (3); female seals herself into nest, starts remex and rectrix moult before laying, emerges with chicks at end of nesting cycle; male delivers food to nest inmates by regurgitation.
Conservation Status
VULNERABLE. CITES II. Locally common, although loss of lowland forest has fragmented its range, especially in S Sulawesi. Generally less susceptible to negative effects of anthropogenic habitat modification than R. cassidix, provided at least some large trees remain (6). Groups occupy home range of 1·5–2 km2, and occurs in Manembonembo Nature Reserve (7), Tangkoko-Dua Saudara Nature Reserve (1), Gunung Ambang Nature Reserve (8), Dumonga-Bone (now Bogani Nani Wartabone) National Park and in Lore Lindu National Park, as well as in Anoa, Lapago, Wahalaka and Wabalamba Forest Reserves on Buton I (6). Still hunted for food, and for keeping as pets.