Geographic Range
Japanese crested ibises once ranged throughout temperate East Asia (from central China
to Hokkaido, Japan and from southeastern Siberia to Taiwan), but are now restricted
to several populations in China. Northern populations migrated south in autumn; more
southern populations were sedentary.
- Biogeographic Regions
- palearctic
Habitat
Wetlands are important foraging areas for Japanese crested ibises. Due to human disturbance,
ibises are thought to have moved from highly populated wetland areas to mountainous
areas. Mountainous regions in the Japanese crested ibis range do not have many wetlands,
so rice paddies are often used for foraging. Habitat preferences change seasonally.
During the breeding season, these ibises forage and roost within their territories,
but in the post-breeding season they may forage in large flocks up to 20 km from roosting
sites. Breeding regions in China are at about 1000 m above sea level, while post-breeding
regions are up to 500 m above sea level.
- Habitat Regions
- temperate
- terrestrial
- Other Habitat Features
- agricultural
Physical Description
Japanese crested ibises are small among ibises, measuring about 56 cm in body length.
The wings are long and the tail rounded. The plumage is white tinged with pink, and
appears pink when seen from below in flight. The bill is long and curved, colored
black with a red tip. The face is featherless and red. The eye is ringed with yellow
and has a red iris. The red to brown legs are relatively short with webbed toes. The
neck is also relatively short and covered with a mane of narrow feathers which hang
to the base of the neck. A large crest sits on the nape. During the breeding season,
the head and upper body turn gray, while the rest of the body remains unchanged.
- Other Physical Features
- endothermic
- homoiothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes alike
Reproduction
Japanese crested ibises are monogamous, remaining in pairs throughout the year.
Courtship behavior begins in January when Japanese crested ibises begin to display.
One bird approaches the other with nesting material in its bill while bobbing its
head. If the other bird accepts the material, the male will stand on the female's
back in a pseudo-copulatory display. This display is repeated if another ibis approaches.
If the material is not accepted, the rejected ibis will carry the material for many
days, soliciting other ibises for pairing. In actual copulation sequences, the pair
will approach each other with crests raised. They then touch beaks and allopreen.
The female crouches and shakes her head, while the male mounts and wags his tail.
- Mating System
- monogamous
Japanese crested ibises breed between March and August, raising one clutch per season.
Clutch size varies between 1 and 5 eggs, averaging 3 eggs. They are laid at 1 or 2
day intervals. Eggs are 6.3 to 6.8 cm long, and weigh 65 to 75 g each. Coloration
is blue-gray with brown spots. Japanese crested ibises nest in mountainous areas.
Both sexes incubate the eggs for 26 to 30 days. They will re-nest if the eggs are
lost to predators. Mean hatching success is 80.2%. Egg losses can be due to infertility,
predation, and human disturbance. Chicks hatch in mid-May with a bald head, light
gray down, and orange-red legs. Offspring grow rapidly, fed on a diet of regurgitated
food from both parents. Chick mortality factors include food shortage, predation,
and human disturbance. At about one month old, chicks will begin to walk on branches
adjacent to the nest. Chicks remain near the nest tree until families gather in flocks
for winter in early September. Fledging tends to occur at 45 days of age. Young become
mature and capable of reproduction at 3 years.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- oviparous
Both sexes construct a twig nest measuring about 50 to 70 cm across, lined with moss
and leaves. In China, Chinese red pine (
Pinus massoniana
) and Chinese cork oak (
Quercus variabilis
) are both preferred nesting trees, although other trees have also been used. Incubation
is also conducted by males and females, beginning in mid-April and lasting about 1
month. Chicks then hatch in mid-May. Both sexes exhibit feeding visits and feeding
bouts throughout the breeding season. Nests are usually at the same sites year after
year.
- Parental Investment
- altricial
-
pre-fertilization
- provisioning
-
protecting
- female
-
pre-hatching/birth
-
provisioning
- female
-
protecting
- male
- female
-
provisioning
-
pre-weaning/fledging
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
-
pre-independence
-
provisioning
- male
- female
-
protecting
- male
- female
-
provisioning
Lifespan/Longevity
The maximum breeding age has been estimated as 16 years. Chicks exhibit about 43%
mortality in their first year. Survival increases to 19% at 1 year, then stays steady
at about 5% for remaining age classes. Egg hatching success is 80.2%. A captive Japanese
crested ibis lived to 26 years old.
Behavior
Japanese crested ibises flock outside of the breeding season. It is thought that Japanese
crested ibises were colonial nesters in the southern part of their range (China),
because the habitat was more suitable and populations were sedentary. Habitats are
more marginal in Japan and the former Soviet Union and populations are migratory there.
All extant Japanese crested ibises are solitary nesters and will defend territory
from rivals.
Allopreening has been observed in Japanese crested ibises. This behavior is initiated
by one individual gently nibbling at the red tip of another’s beak. The head, neck,
and upper back of the recipient is allopreened. The crest of the recipient is usually
raised when the nape is allopreened.
Japanese crested ibises are unique in that breeding (nuptial) plumage occurs as a
result of cosmetic application of a waxy, tar-like substance. The behavior of application
is known as ‘daubing’. Daubing behavior follows bathing, and consists of applying
the dark substance to the feathers of the head, neck, back, and upper wing coverts.
The substance is excreted from specialized skin on the head and neck. Daubing behavior
is exhibited during the winter, just prior to the first courtship behaviors. The development
of nuptial plumage in Japanese crested ibises seems to be unique among birds.
- Key Behaviors
- flies
- diurnal
- motile
- migratory
- sedentary
- territorial
Communication and Perception
While feeding, resting, and preening, Japanese crested ibises are silent. Before flight,
a low ‘gak’ is emitted while in an upright posture. The call is repeated several times
before taking to the air. If flushed, these ibises will emit a rapid series of ‘gak-gak-gak’
calls. This seems to be a high intensity alarm call, while the single ‘gak’ may function
as an alarm as well as a contact call.
The nest is defended against conspecific rivals by threat displays including wing
flapping, head extension, stretch-and-snap, and pursuit flight displays. The crest
is used in sexual display.
Food Habits
Wetlands are important foraging areas for Japanese crested ibises. Animals consumed
include fish (
carp
,
catfish
,
eels
,
weatherfish
),
frogs
,
newts
, river crabs,
crayfish
,
water-scavenger beetles, diving beetles, beetle larvae
,
crickets
,
snails
,
mussels
, and
earthworms
. Stomach contents from Korea have shown rice as well. Supplemental feeding with
loach
has also improved survival.
Japanese crested ibises feed in shallow flooded muddy regions, not deeper than their
leg length (10 to 15 cm). Beaks are probed into the mud while the ibises walk slowly,
stopping as they encounter a food item. Once a food item is taken, it is shaken several
times in the water before being swallowed. A preference has been noted for feeding
along mud walls of rice paddies. If a pair of ibises locates a cluster of prey, the
larger individual will dominate the find. Throughout winter, ibises will visit several
feeding areas within the same general area.
- Primary Diet
-
carnivore
- piscivore
- insectivore
- eats non-insect arthropods
- molluscivore
- vermivore
- Animal Foods
- amphibians
- fish
- insects
- terrestrial non-insect arthropods
- mollusks
- terrestrial worms
- aquatic crustaceans
- Plant Foods
- seeds, grains, and nuts
Predation
Japanese crested ibises are preyed upon by snakes (especially king ratsnakes (
Elaphe carinata
), Siberian weasels (
Mustela sibirica
), yellow-throated martens (
Martes flavigula
), and large birds of prey such as eagles, kites, goshawks, and kestrels. Crows have
been documented destroying nests and preying on eggs.
Ecosystem Roles
Japanese crested ibises are predators of smaller vertebrate and invertebrate animals.
They also act as hosts to a variety of parasites.
Economic Importance for Humans: Positive
Endangered species, like Japanese crested ibises, draw ecotourism interest. Local economies may benefit from having Japanese crested ibises nest near them.
- Positive Impacts
- ecotourism
- research and education
Economic Importance for Humans: Negative
Japanese crested ibises may trample newly planted rice paddies while foraging, and
stomach contents have found rice as well. However, the rarity of these birds make
their impact on crops negligible.
- Negative Impacts
- crop pest
Conservation Status
Japanese crested ibises were thought to be extinct in the wild until 1981, when a
few wild birds were discovered in the mountains of Yang County, Shaanxi Province,
China. Since rediscovery, measures have been taken to protect the remnant population.
Nests are observed and predators driven away by volunteers. During food shortages,
loach
are stocked in local rice paddies. Nestlings too weak to compete with siblings for
food are given artificial feedings. Education has also been undertaken on preserving
habitat, banning hunting, and forbidding pesticide use. The wild population is now
experiencing an upward growth trend. A successful captive breeding program had been
ongoing since 1995. Two eggs were laid in Tama Zoological Park in Tokyo in March 2008.
According to one population viability analysis, the major parameters affecting the
fate of the population are environmental variation and catastrophes. Habitat loss,
hunting, and environmental pollution were the dominant factors which brought about
the catastrophic decline since the late nineteenth century. Low genetic diversity
from this bottleneck may cause a limited ability to tolerate a wide range of environmental
extremes and diseases, hindering reintroduction efforts in other regions of former
ibis range.
Other Comments
Japanese crested ibises are known as ‘toki’ in Japan. In Japanese, ‘toki-iro’ (toki-color) is the characteristic pink-ish hue seen as the ibis flies overhead. The scientific name Nipponia nippon comes from the Japanese name for Japan, "Nippon."
Additional Links
Contributors
Tanya Dewey (editor), Animal Diversity Web.
William Severud (author), Northern Michigan University, Alec R. Lindsay (editor, instructor), Northern Michigan University.
- Palearctic
-
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- temperate
-
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
- terrestrial
-
Living on the ground.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- mountains
-
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
- marsh
-
marshes are wetland areas often dominated by grasses and reeds.
- swamp
-
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
- agricultural
-
living in landscapes dominated by human agriculture.
- endothermic
-
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
- bilateral symmetry
-
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
- monogamous
-
Having one mate at a time.
- iteroparous
-
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
- seasonal breeding
-
breeding is confined to a particular season
- sexual
-
reproduction that includes combining the genetic contribution of two individuals, a male and a female
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- altricial
-
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
- diurnal
-
- active during the day, 2. lasting for one day.
- motile
-
having the capacity to move from one place to another.
- migratory
-
makes seasonal movements between breeding and wintering grounds
- sedentary
-
remains in the same area
- territorial
-
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
- visual
-
uses sight to communicate
- acoustic
-
uses sound to communicate
- ecotourism
-
humans benefit economically by promoting tourism that focuses on the appreciation of natural areas or animals. Ecotourism implies that there are existing programs that profit from the appreciation of natural areas or animals.
- carnivore
-
an animal that mainly eats meat
- piscivore
-
an animal that mainly eats fish
- insectivore
-
An animal that eats mainly insects or spiders.
- molluscivore
-
eats mollusks, members of Phylum Mollusca
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- acoustic
-
uses sound to communicate
- chemical
-
uses smells or other chemicals to communicate
References
Archibald, G., S. Lantis. 1978. Conservation of the Japanese crested ibis. Proceedings of the 1978 Conference of the Colonial Waterbird Group, 2: 1-15.
Fennell, C., B. King. 1964. New occurrences and recent distributional records of Korean birds. The Condor , 66: 239-246.
Li, X., D. Li, Y. Li, Z. Ma, T. Zhai. 2002. Habitat evalution for crested ibis: a GIS-based approach. Ecological Research , 17: 565-573.
Li, X., D. Li. 1998. Current state and the future of the crested ibis ( Nipponia nippon ): a case study by population viability analysis. Ecological Research , 13: 323-333.
Sanada, K. 2002. "Has the Japanese Crested Ibis Been Saved from Extinction?" (On-line). Nipponia. Accessed April 06, 2008 at http://web-japan.org/nipponia/nipponia23/en/topic/index.html .
Shi, D. 1991. The diet of the crested ibis and the food abundance during wandering season. Journal of Northwest University (additional edition) , 21: 37-42 (in Chinese).
Wingfield, J., S. Ishii, M. Kikuchi, S. Wakabayashi, H. Sakai, N. Yamaguchi, M. Wada, K. Chikatsuji. 2000. Biology of a critically endangered species, the toki (Japanese crested ibis) Nipponia nippon . Ibis , 142: 1-11.
Yu, X., N. Liu, Y. Xi, B. Lu. 2006. Reproductive success of the crested ibis Nipponia nippon . Bird Conservation International , 16: 325-343.
Zhang, B., S. Fang, Y. Xi. 2004. Low genetic diversity in the endangered crested ibis Nipponia nippon and implications for conservation. Bird Conservation International , 14: 183-190.
2003. Japanese Ibis Nipponia nippon . Pp. 298-299 in Grzimek's Animal Life Encyclopedia , Vol. 8, 2nd Edition. Detroit, New York, San Diego, San Francisco, Cleveland, New Haven, Waterville, London, Munich: Thomson Gale.