Overview

Distribution

Range Description

Buceros bicornis has a wide distribution, occurring in China (rare resident in west and south-west Yunnan and south-east Tibet), India (locally fairly common, but declining), Nepal (local and uncommon, largely in protected areas), Bhutan (fairly common), Bangladesh (vagrant), Myanmar (scarce to locally common resident throughout), Thailand (widespread, generally scarce but locally common), Laos (formerly common; currently widespread but scarce and a major decline has clearly occurred), Vietnam (rare and declining resident), Cambodia (rare), Peninsular Malaysia (uncommon to more or less common) and Indonesia (uncommon on Sumatra).
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Geographic Range

Buceros bicornis is found in mainland Southeast Asia, the Malay Peninsula and Indonesia. They are breeding residents in Bhutan, Cambodia, China, India, Indonesia, Laos, Malaysia, Myanmar, Nepal, Thailand and Vietnam. In India, they and several other hornbill species live in the Western Ghats mountain range and forests in both the northeastern and southern regions.

Biogeographic Regions: oriental (Native )

  • 1990. Endangered Animals of Thailand. Boca Raton, Florida: CRC Press.
  • 2007. Popular Handbook of Indian Birds. Great Britain: Horney Press.
  • Datta, A. 1998. Hornbill abundance in unlogged forest, selectively logged forest and a forest plantation in Arunachal Pradesh, India. Oryx, Volume: 32, Issue: 4: 285 - 294.
  • Mobley, J. 2008. Birds of the World. Tarrytown, NY: Marshall Cavendish Corporation.
  • Raman, T., D. Mudappa. 2003. Correlates of hornbill distribution and abundance in rainforest fragments in the southern Western Ghats, India. Bird Conservation International, Volume: 13, Issue: 3: 199 - 212.
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Physical Description

Morphology

Physical Description

Great hornbills are fairly large, ranging from 95 to 120 cm in length and featuring a wingspan of 151 to 178 cm. On average, they weigh 3 kg. They are vividly colored and easily recognizable. The body, head, and wings are primarily black; the abdomen and neck are white. The tail is white and is crossed by a subterminal black band. A preen gland near the tail secretes tinted oil, which is spread across the feathers by the bird during grooming. This may give the bill, neck, casque, and tail and wing feathers coloration varying from yellow to red. The most recognizable feature of hornbills is the casque, which is a hollow structure located on top of the bill. It may be used by males to fight with other males and attract females. Like many other hornbills, these birds have prominent eyelashes.

Males and females are similar except that the irises of males are red while those of females are white, and males have slightly larger bills and casques.

The feature that distinguishes B. bicornis from other species is its greatly curved bill and prominent casque.

Average mass: 3 kg.

Range length: 95 to 120 cm.

Range wingspan: 151 to 178 cm.

Other Physical Features: endothermic ; homoiothermic; bilateral symmetry

Sexual Dimorphism: sexes alike; sexes colored or patterned differently; ornamentation

  • Golding, R., M. Williams. 1986. Breeding the Great Indian Hornbill. International Zoo Yearbook, Volume 24/25: 248 - 252.
  • James, D., R. Kannan. 2009. Nesting Habitat of the Great Hornbill (Buceros Bicornis) in the Anaimalai Hills of Southern India. Wilson Journal of Ornithology, Volume: 121 , Issue: 3: 485-492.
  • Raman, T. 1998. Aerial Casque-butting in the Great Hornbill. Forktail, Volume 13: 123 - 124.
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Ecology

Habitat

Habitat and Ecology

Habitat and Ecology
This species frequents evergreen and mixed deciduous forests, ranging out into open deciduous areas to visit fruit trees and ascending slopes to at least 1,560 m. The abundance of this species tends to be correlated with the density of large trees, and it is therefore most common in unlogged forest.

Systems
  • Terrestrial
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Habitat

Great hornbills are arboreal and live mainly in wet, tall, evergreen forests. Old-growth trees that extend beyond the height of the canopy are preferred for nesting. The height of the tree and the presence of a natural cavity large enough to hold a female and her eggs are more important than the type of tree. The same nesting site is used year after year if possible. They are known to inhabit elevations of 600 to 2000 m.

Range elevation: 600 to 2000 m.

Habitat Regions: tropical ; terrestrial

Terrestrial Biomes: forest ; rainforest

  • Datta, A., G. Rawat. 2003. Foraging Patterns of Sympatric Hornbills during the Nonbreeding Season in Arunachal Pradesh, Northeast India. Biotropica, Volume: 35, Issue: 2: 208 - 218.
  • Kannan, R., D. James. 1999. Fruit Phenology and the Conservation of the Great Pied Hornbill (Buceros bicornis) in the Western Ghats of Southern India. Biotropica, Volume: 31, Issue: 1: 1677 - 177.
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Trophic Strategy

Food Habits

Members of this species are predominantly frugivores that feed on both lipid-rich and sugar-rich fruits but feed on small mammals, birds, amphibians, reptiles, and insects as well. The lipid-rich fruits include those in the genus Knema and Myristica commonly known as nutmeg trees, and several in the family Lauraceae such as Beilschmiedia. Though these lipid-rich fruits may be available throughout the year, they are particularly abundant during the breeding season. As a result, B. bicornis relies on these fruits as its primary source of energy during the breeding season when energy needs are significantly higher for both the parents and young. This is also true for other hornbill species in the same region, such as Malabar gray hornbills (Ocyceros griseus).

During the rest of the year, great hornbills rely on sugar-rich fruits such those of Vitex altissima and several species in the genus Ficus (fig trees). Figs account for the majority of fruit consumption of B. bicornis throughout the year. Great hornbills have been known to protect fig trees from other birds such as wreathed hornbills (Rhyticeros undulatus).

Animal Foods: birds; mammals; amphibians; reptiles; insects

Plant Foods: fruit

Primary Diet: herbivore (Frugivore )

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Associations

Ecosystem Roles

Due to its large gape, Buceros bicornis is able to transport and disperse seeds of trees in the genus Myristica, which tend to be too large for other organisms. These trees rely on B. bicornis for seed dispersal since only a few other birds (such as Ocyceros griseus) are able to ingest the seeds intact to later disperse. They also impact populations of small mammals, birds, amphibians, reptiles and insects that they occasionally consume.

Ecosystem Impact: disperses seeds

  • Gale, G., S. Thongaree. 2006. Density Estimates of Nine Hornbill Species in a Lowland Forest Site in Southern Thailand. Bird Conservation International, Volume: 16 , Issue: 1: 57-69.
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Predation

Buceros bicornis has few if any natural predators due to its relatively large size and the fact that members of this species tend to occupy the canopy. However, humans occasionally hunt and kill great hornbills for their meat, casque, and feathers for subsistence, medicinal, or ritualistic purposes.

Known Predators:

  • 2004. The Status and Conservation of Hornbills in Cambodia. Bird Conservation International, Special Issue S1: S5-S11.
  • Azua, J., N. Czekala. 2003. Reproductive assessment of the great hornbill (Buceros bicornis) by fecal hormone analysis. Zoo Biology, Volume: 22, Issue: 2: 135 - 145.
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Life History and Behavior

Behavior

Communication and Perception

Except for the time during nesting season, Buceros bicornis vocalizes very loudly. The sounds they produce can be described as "cackling" or "roaring." Great hornbills are most vocal within large, communal night roosts. Roosts are often hypothesized to be "information hubs" where individuals can share information regarding good feeding sites, for example. Pairs of great hornbills use duets as part of courtship, where a male and female alternate calls to each other. The location of individuals can be identified by sound alone due to their vocalizations combined with the characteristic "whooshing" sound produced by their flight. This unique flight sound is produced from lack of flight feather coverts.

Male great hornbills use tactile forms of communication to compete for mates. Males collide bill casques, often in flight, during the time preceding the breeding season. The size of male bill casques also likely serves as visual communication to potential mates. Like all birds, great hornbills perceive their environments through visual, tactile, auditory and chemical stimuli.

Communication Channels: visual ; tactile ; acoustic

Other Communication Modes: duets

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Life Expectancy

Lifespan/Longevity

Buceros bicornis may live up to fifty years of age in captivity, but range from 35 to 40 in the wild. Though B. bicornis may occasionally be hunted by man, they lack natural predators and their food is often plentiful. These two things allow for a relatively long lifespan.

Typical lifespan

Status: wild:
35 to 40 years.

Typical lifespan

Status: captivity:
50 (high) years.

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Lifespan, longevity, and ageing

Maximum longevity: 33.4 years (captivity)
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Reproduction

Reproduction

Great hornbills breed between the months of February and May. Male casque size is important in attracting and fighting for mates. Males compete for females by butting into each other in the presence of a female prior to the breeding season. This could possibly be a display of superiority in competition for a mate. Mates, or potential mates, also perform duets where the male calls, the female replies, and they continue on in a loud volley. Buceros bicornis tends to be monogamous, and the pair remains together throughout their lives.

Mating System: monogamous

A unique feature of Buceros bicornis and some other hornbill species such as Buceros rhinoceros is the way that the female incubates and cares for her eggs. During the breeding period, which lasts between February and May, a monogamous pair chooses a tree in which to lay the eggs. This tree is usually a very tall, old-growth tree and the same one is used every year if possible.

After finding a hole in the tree that is large enough, the female uses both her own feces and her mate's to cover the entrance from the inside, thus confining herself inside. She makes a small slit through which the male provides food. In captivity, B. bicornis may use soft fruits such as bananas in addition to feces to cover the hole. While inside the hole, the female lays and then incubates on average two eggs. The male provides fruits from trees in the genus Beilschmiedia, which are widely available during the breeding season; she receives no nutrients other than this. In other hornbill species such as Buceros hydrocorax, other non-breeding birds in addition to the male may provide assistance by bringing fruit to a female incubating her eggs. The incubation period usually lasts between 38 and 40 days. Protected within the tree, the female completes a full molt which renders her flightless for a period of time.

After the chicks hatch, the female remains confined in the tree for around five weeks when she emerges to help the male gather food for the growing young. The young re-seal themselves within the cavity after the female leaves. For the next two weeks, the both parents provide food for the young. After the young emerge, the parents continue to feed them until they reach roughly 15 weeks of age, at which point they are considered independent.

Breeding interval: Great Hornbills breed once a year.

Breeding season: Breeding occurs between February and May.

Range eggs per season: 1 to 2.

Average eggs per season: 2.

Range time to hatching: 38 to 40 days.

Average time to independence: 15 weeks.

Key Reproductive Features: seasonal breeding ; gonochoric/gonochoristic/dioecious (sexes separate)

Parental investment in this species consists of providing food for young throughout the time period between hatching and independence. The mother is confined within the nest tree for a few weeks during the pre-hatching period, which usually lasts a few weeks, and for approximately five weeks after hatching.

During these periods, the male provides food while the female and young are protected in the tree. The male must forage extensively for lipid-rich fruits in order to feed himself as well as the female and the young. The male and female continue to feed the young throughout the pre-independence period until roughly fifteen weeks of age.

Great hornbills also invest energy in defending a nesting territory. They are only territorial during the breeding season, and may defend a 100 m area around the nest.

Parental Investment: altricial ; male parental care ; female parental care ; pre-fertilization (Provisioning, Protecting: Female); 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); post-independence association with parents

  • Choy, P. 1980. Breeding the Great Indian hornbill Buceros bicornis at Jurong Bird Park. International Zoo Yearbook, Volume: 20, Issue: 1: 204 - 206.
  • Datta, A., G. Rawat. 2003. Foraging Patterns of Sympatric Hornbills during the Nonbreeding Season in Arunachal Pradesh, Northeast India. Biotropica, Volume: 35, Issue: 2: 208 - 218.
  • Golding, R., M. Williams. 1986. Breeding the Great Indian Hornbill. International Zoo Yearbook, Volume 24/25: 248 - 252.
  • James, D., R. Kannan. 2007. Wild Great Hornbills (Buceros bicornis) Do Not Use Mud to Seal Nest Cavities. The Wilson Journal of Ornithology, Volume 119, Issue 1: 118 - 121.
  • Mobley, J. 2008. Birds of the World. Tarrytown, NY: Marshall Cavendish Corporation.
  • Poulsen, H. 1970. Nesting Behaviour of the Black-Casqued Hornbill Ceratogymna atrata and the Great Hornbill Buceros bicornis L.. Ornis Scandinavica, Volume: 1, Issue: 1: 11 - 15.
  • Raman, T. 1998. Aerial Casque-butting in the Great Hornbill. Forktail, Volume 13: 123 - 124.
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Molecular Biology and Genetics

Molecular Biology

Statistics of barcoding coverage: Buceros bicornis

Barcode of Life Data Systems (BOLDS) Stats
Public Records: 0
Species: 2
Species With Barcodes: 1

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Conservation

Conservation Status

IUCN Red List Assessment


Red List Category
NT
Near Threatened

Red List Criteria

Version
3.1

Year Assessed
2008

Assessor/s
BirdLife International

Reviewer/s
Gilroy, J., Butchart, S.

Contributor/s

Justification
Although this species has a large range, it occurs at low densities and is patchily distributed. It is likely to be declining moderately rapidly throughout its range, and is therefore considered Near Threatened.

History
  • 2004
    Near Threatened
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Conservation Status

Buceros bicornis is considered "near threatened" on the IUCN Red List. The biggest threat to this species is habitat destruction, and particularly the removal of the old-growth trees that these birds require for nesting. Their large size and distinctive sounds make great hornbills relatively easy targets for hunters, who value them for their meat, feathers and casque, which is used for ornamental purposes among natives. They are listed under CITES appendix I which restricts trade of the species for exceptional purposes only.

CITES: appendix i

IUCN Red List of Threatened Species: near threatened

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Population

Population Trend
Decreasing
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Threats

Threats

Major Threats
Logging is likely to have impacted this species throughout its range, particularly as it shows a preference for forest areas with large trees that may be targeted by loggers. Forest clearance for agriculture is also likely to have contributed to declines. It is particularly susceptible to hunting pressure as it is large, visits predictable feeding sites (such as fruiting trees) and its casques are kept or sold as trophies.
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Management

Conservation Actions

Conservation Actions
Conservation Actions Underway
CITES Appendix I.

Conservation Actions Proposed
Monitor populations across the range to determine the magnitude of declines and rates of range contraction. Campaign for the protection of remaining extensive tracts of lowland forest throughout the range.

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Relevance to Humans and Ecosystems

Benefits

Economic Importance for Humans: Negative

There are no known adverse effects of Buceros bicornis on humans.

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Economic Importance for Humans: Positive

Buceros bicornis is kept in zoos in various parts of the world. Efforts to breed this species in captivity are generally not successful.

The casque of B. bicornis is used as an ornamental piece by natives. They are also occasionally hunted for their meat and feathers for subsistence, ritualistic or medicinal purposes.

They are also an important seed disperser which aids in forest propagation.

Positive Impacts: body parts are source of valuable material

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Wikipedia

Great Hornbill

The Great Hornbill (Buceros bicornis) also known as Great Indian Hornbill or Great Pied Hornbill, is one of the larger members of the hornbill family. Great Hornbills are found in the forests of Nepal, India, the Malay Peninsula and Sumatra, Indonesia. Their impressive size and colour have made them important in many tribal cultures and rituals. The Great Hornbill is long-lived, living for nearly 50 years in captivity. They are predominantly frugivorous although they are opportunists and will prey on small mammals, reptiles and birds.

Contents

Description

The iris, underside of the casque and orbital skin colours vary between the sexes

The Great Hornbill is a large bird, 95–120 cm (38–47 in) long, with a 152 cm (60 in) wingspan and a weight of 2.15–4 kg (4.7-8.8 lbs). It is the heaviest, but not the longest, Asian hornbill. The most prominent feature of the hornbill is the bright yellow and black casque on top of its massive bill. The casque appears U-shaped when viewed from the front and the top is concave with two ridges along the sides that form points in the front, a reference to which is made in the Latin species epithet bicornis. The casque is hollow and serves no known purpose although they are believed to be the result of sexual selection. Male hornbills have been known to indulge in aerial casque butting, with birds striking each other in flight.[3] Females are smaller than males and have bluish-white instead of red eyes although the orbital skin is pinkish. Like other hornbills, they have prominent "eyelashes". The back of the casque is reddish in females while the underside of the front and back of the casque is black in males. The male spreads the preen gland secretion which is yellow onto the primaries and bill to give them the bright yellow colour.[4] The commissure of the beak is black and has a serrated and worn edge with age. The wing beats are heavy and the sound produced by birds in flight can be heard from a distance. The sound produced has been likened to the puffing of a steam locomotive starting up. The flight involves stiff flaps followed by glides with the fingers splayed and upcurled. They are sometimes known to fly at great height over forests.[5][6]

Illustration by T. W. Wood (1823-1903) showing the eyelashes, worn bill edge and the concave casque with ridged sides

The species was formerly broken into subspecies cavatus from the Western Ghats, nominate form from the sub-Himalayan forests is sometimes named as subspecies homrai. The subspecies from Sumatra has sometimes been considered as cristatus.[7] The variation across populations is mainly in size, with Himalayan birds being larger than the those from further south and the species is now usually considered monotypic.[8][9]

Like other members of the hornbill family, they have highly pneumatized bones, with hollow air cavities extending to the tips of their wing bones. This anatomical feature was noted by Richard Owen who dissected a specimen at the Zoological Society of London that died in 1833.[10]

Distribution and habitat

The distribution of the species is fragmented over its range in South and Southeast Asia. In South Asia they are found in a few forest areas in the Western Ghats and in the forests along the Himalayas. Their distribution extends into Thailand, Burma, Malaya and Sumatra.[11] Their habitat is dense old growth (unlogged) forests in hilly regions.[12][13] They appear to be dependent on large stretches of forest unlike many of the smaller hornbills.[14]

In Thailand the home ranges of males was found to be about 3.7 km² during the breeding season and about 14.7 km² during the non-breeding season.[15]

Behaviour and ecology

Food and feeding

Captive feeding in Rotterdam

Great Hornbills are usually seen in small parties with larger groups sometimes aggregating at fruit trees. A congregation of 150 to 200 birds has been recorded in southeastern Bhutan.[5] In the wild, the Great Hornbill's diet consists mainly of fruit. Figs are particularly important as a food sources.[16] Vitex altissima has been noted as another important species. They also forage on lipid-rich fruits of the Lauraceae and Myristicaceae families such as Persea, Alseodaphne and Myristica.[17] They obtain the water that they need entirely from their diet of fruits. They are important dispersers of many forest tree species.[18] They will also eat small mammals, birds,[19] small reptiles and insects.[20] It has been observed that lion-tailed macaques forage alongside these hornbills.[21]

They forage along branches, moving along by hopping, looking for insects, nestling birds, small lizards, tearing up bark and examining them. Prey are caught, tossed in the air and swallowed. A rare squirrel, the Travancore flying squirrel Petinomys fuscocapillus has been noted in the diet of the species while Collared Scops Owl Otus bakkamoena, Jungle Owlet Glaucidium radiatum and Grey-fronted Green Pigeon Treron pompadora have been noted as prey birds in the Western Ghats.[22]

Breeding

Male feeding the female inside the nest

During the breeding season they become very vocal. They make loud duets. These calls begin with a loud "kok" about once a second given by the male and joined in by a female. The pair then calls in unison turning into a rapid mixture of roars and barks.[22] They prefer mature forests for nesting. Large, tall and old trees, particularly emergents that rise above the canopy appeared to be preferred for nesting.[23][24]

The Great Hornbills form monogamous pair bonds and live in small groups of 2-40 individuals. Group courtship displays involving up to 20 birds have been observed.[25]

Female hornbills build nests in hollows of large tree trunks and the opening is sealed with a plaster made up mainly of feces.[7][26][27] She remains imprisoned in her nest until the chicks are semi-developed relying on the male to bring her food. During this period the female undergoes a complete moult. The young chicks are devoid of feathers and appear very plump. She is fed by her mate through a slit in the seal. The clutch consists of one or two eggs she incubates for 38–40 days. The female voids feces through the nest slit and young follow the same nest sanitation behaviour after they are two weeks old.[22] Once the female emerges out of the nest, it is sealed again by the chicks.[8]

The young birds have no trace of a casque. After the second year, the front extremity separates from the culmen and in the third year becomes a transverse crescent with the two edges growing outwards and upwards while the anterior gets broader to equal the hind end in width. The full development takes five years.[28]

Roosting

Roost sites are used regularly and birds will arrive punctually at sunset from long distances, following the same routes each day. Several tall trees in the vicinity may be used, the birds choosing the highest branches with little foliage. They jockey for positions until late at dusk. When sleeping they draw their neck back and the bill is held upwards at an angle.[5]

In captivity

At Palmitos Park, Spain

Very few hornbills are held in captivity and few of them breed well. The females at the nests are extremely easy to capture and wild caught birds are female biased. Breeding them in captivity has been notoriously difficult with fewer than a dozen successful attempts. Their extreme selectivity for mates and the long and strong pair bonds make them difficult to maintain for breeding.[29][30][31][32]

In captivity hornbills eat fruits and meat and a healthy diet is made up in most part, by fruit and some source of protein. A few have been tamed in captivity but hornbill behavior in captivity is described as high-strung. Captive specimens may bask in the sun with outstretched wings.[33]

Conservation status

Due to habitat loss and hunting in some areas, the Great Hornbill is evaluated as Near Threatened on the IUCN Red List of Threatened Species.[1] It is listed on Appendix I of CITES. Declines in population have been noted in many areas such as Cambodia.[34] Molecular approaches to the study of their population diversity have been attempted.[35]

In culture

Tribals threaten the Great Indian Hornbills with their desire for its various parts. The beaks and head are used in charms and the flesh is believed to be medicinal. The squabs are considered a delicacy.[5] Tribesmen in parts of northeastern India and Borneo use their feathers for head-dresses, and their skulls are often worn as decorations.[36][37] Their flesh is considered unfit for eating by the Nagas with the belief that they produce sores on their feet as in the bird. When dancing with the feathers of the hornbill, they avoid eating vegetables as it is also believed to produce the same sores on the feet.[38] Conservation programmes have attempted to provide tribes with feathers from captive hornbills and ceramic casques to substitute natural ones.[39]

The hornbills is called "homrai" in Nepal (giving the name of that subspecies) and "banrao" both meaning "King of the forest".[40]

Use as a symbol

Photo of "William", who lived at the premises of the Bombay Natural History Society and was the inspiration for the logo of the Society.[41]

The Great Hornbill is the State bird of Chin State in Myanmar, and Kerala and Arunachal in India.

A Great Hornbill by the name of William (pictured) was the model for the logo of the Bombay Natural History Society (BNHS) and the name for their building. Sir Norman Kinnear described William as follows in the obituary of W S Millard: “Every visitor to the Society's room in Apollo Street will remember the great Indian Hornbill, better known as the "office canary" which lived in a cage behind Millard's chair in Phipson & Co.'s office for 26 years and died in 1920. It is said its death was caused by swallowing a piece of wire, but in the past "William" had swallowed a lighted cigar without ill effects and I for my part think that the loss of his old friend was the principal cause." [42][43]

Other sources

  • Kannan,R (1994) Ecology and Conservation of the Great Pied Hornbill (Buceros bicornis) in the Western Ghats of southern India. Ph.D. Thesis, University of Arkansas, Fayetteville.
  • Kannan,Ragupathy (1994) Conservation ecology of the Great Hornbill in the Western Ghats, southern India. OBC Bull. 19:13.
  • Poonswad, P. 1995. Nest site characteristics of four sympatric species of hornbills in Khao Yai National Park, Thailand. Ibis 137: 183-191.
  • Poonswad, P. and A. Tsuji. 1994. Ranges of males of the Great Hornbill (Buceros bicornis), Brown Hornbill (Ptilolaemus tickelli) and Wreathed Hornbill (Rhyticeros undulatus) in Khao Yai National Park, Thailand. Ibis 136: 79-86.

References

  1. ^ a b BirdLife International (2008). Buceros bicornis. In: IUCN 2008. IUCN Red List of Threatened Species. Downloaded on 3 Oct 2009.
  2. ^ Hodgson,BH (1833). "Description of the Buceros Homrai of the Himalaya". Asiat. Res. 18 (2): 169–188. 
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