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Bombina orientalis


By Todd Szcodronski

Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Class: Amphibia
Family: Bombinatoridae
Genus: Bombina
Species: Bombina orientalis

Geographic Range

Bombina orientalis is found in northeast China (the provinces of Heilongjiang, Hebei, Shandong, Anhui, and Lianoning). These toads can also be found in Korea, Thailand, and southern Japan (the islands of Kiushiu and Tsushima). Bombina orientalis also occurs in the Primorye and Khabarovsk regions of Russia. (Kuzmin and Vredenburg, 2003)

Biogeographic Regions
palearctic (Native ); oriental (Native )

Habitat

Oriental fire-bellied toads occupy a variety of different habitats. They live at high elevations in spruce, pine or deciduous forests, river valleys, swampy bushlands, and open meadows. Bombina orientalis lives in or around various water types, including stagnant and running water in lakes, ponds, swamps, streams, springs, even puddles and ditches. Typically, this species stays relatively close to water, but in late summer they occur up to a few hundred meters from water. (Kuzmin and Vredenburg, 2003)

Habitat Regions
temperate ; terrestrial ; freshwater

Terrestrial Biomes
forest

Aquatic Biomes
lakes and ponds; rivers and streams; temporary pools

Wetlands
marsh ; swamp ; bog

Other Habitat Features
riparian

Physical Description

Range length
3.5 to 8 cm
(1.38 to 3.15 in)

Oriental fire-bellied toads are dark-colored dorsally, ranging from brownish-gray to bright green. When the dorsal surface is colored more vividly, dark spots are typically also present. The ventral surface is brightly colored, usually with dark spots over brilliant red-orange or yellow reticulated patterns (hence the name "fire-bellied"). The pupils are triangular. The skin is covered in tubercles (warts), except on the ventral surface, where tubercles are only present near the cloaca (the terminal part of the gut). Of the three species in the genus Bombina, Oriental fire-bellied toads have the most pronounced tubercles. Tubercles on the ventral side of the animal are elevated and acute, sometimes feeling like sharp needles. These toads have no tympanic membrane. (Hickman, et al., 2003; Kuzmin and Vredenburg, 2003; Miller, 2002)

Females are generally larger than males. During the breeding season, males develop nuptial pads on their first and second fingers, have more tuberculate skin, and have thicker forearms. (Kuzmin and Vredenburg, 2003; Miller, 2002)

Other Physical Features
ectothermic ; heterothermic ; bilateral symmetry ; poisonous

Sexual Dimorphism
female larger; sexes shaped differently

Development

Oriental fire-bellied toad females lay eggs in clusters of 3 to 45. These clusters are deposited every 7 to 10 days. with a total clutch size of 38 to 257 eggs. Typically, eggs are laid on submerged plants near water's edge. Eggs hatch after a period of 3 to 10 days. In the first week following hatching, the tiny larvae absorb their yolk sacs. Oriental fire-bellied toad tadpoles have a gill slit on the ventral surface that projects outward, this gill slit is called a spiracle. After about 6 to 8 weeks, the hind legs and the lungs start to take shape. After 10 to 14 weeks, tadpoles reach about 3.5 cm in length and begin to metamorphose. After the 12th week, they start to emerge from the water and lose their tails. The transformation process into an adult toad takes approximately 5 months. (Kuzmin and Vredenburg, 2003; Miller, 2002)

Reproduction

Males court females by continuously calling while floating in shallow water. The mating call sounds like a bark and lasts about twelve seconds. Males sit and croak until a female approaches for mating. (Miller, 2002)

In the wild, there are often more males than females at breeding sites, sometimes as many as ten males for every female. Waiting males jumps onto the back of passing toads, hoping it to be a female. Inevitably, males sometimes jump on other males. The target male lets out a loud croak to indicate a mistake has been made. When a female is encountered, the male and female enters amplexus. Females swim around with the male hanging on, fertilizing the eggs as she lays them. (Miller, 2002)

Mating System
polygynandrous (promiscuous)

Breeding interval
Breeding may occur multiple times during a year.

Breeding season
Breeding occurs throughout the warm season, from May to mid-August.

Range number of offspring
38 to 257

Range time to hatching
3 to 10 days

After fertilization, the jelly layers of the eggs absorb water and swell. The eggs remain in this "jelly" state until hatching. Breeding begins with warming weather in the spring and continues throughout the summer. Breeding occurs from May through mid-August eggs hatch after 3 to 10 days. Most hatching occurs in June and July. Females are capable of laying more than one clutch per season. They deposit from 38 to 257 eggs in portions from 3 to 45 eggs every 7 to 10 days. In captivity, the breeding season begins after a cooling winter period with simulated rain. (Hickman, et al., 2003)

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

Bombina orientalis larvae hatch 3 to 10 days after egg laying. There is no direct parental care. The young are left to fend for themselves following hatching. Indirectly, females can influence development of their young by varying the environment the eggs are placed in and energy investment in the eggs. Egg size and water temperature are two such factors. In cold water, larvae that developed from larger eggs had greater fitness than those that developed from small eggs. In warmer environments, larvae that developed from small eggs had greater fitness than those that developed from large eggs. (Kaplan, 1992)

Parental Investment
no parental involvement; pre-fertilization (Provisioning, Protecting: Female)

Lifespan/Longevity

Range lifespan
Status: wild

20 (high) years

Range lifespan
Status: captivity

30 (high) years

Average lifespan
Status: captivity

2.3 years
[External Source: Max Planck Institute for Demographic Research]

Bombina orientalis can live up to a maximum of 30 years in captivity. Maximum longevity in the wild is estimated at 20 years. ("The Oriental Fire-bellied Toad", 2004)

Behavior

Oriental fire-bellied toads hibernate from late September to late April or May. They hibernate in groups of one to six individuals, usually on land inside rotten trees, stone piles, and leaves, but sometimes in streams. They are typically active during the day. (Kuzmin and Vredenburg, 2003)

Key Behaviors
terricolous; saltatorial ; natatorial ; diurnal ; sedentary ; hibernation ; solitary

Home Range

In captivity, Oriental fire-bellied toads are aggressive and territorial. Home ranges in the wild are not known. Population densities in the wild can reach 8 individuals per square meter in the central part of their range. (Kuzmin and Vredenburg, 2003; Miller, 2002)

Communication and Perception

Vocalizations are the primary form of communication and are mostly used during the mating season. Oriental fire-bellied toads have a soft, musical call that sounds like a tapering "oop...oop...ooop." Males croak to attract females, and to warn other males of mistaken identity. (Miller, 2002)

Like most frogs and toads, Oriental fire-bellied toads use vision primarily to detect prey. (Miller, 2002)

Communication Channels
visual ; acoustic

Other Communication Modes
choruses

Perception Channels
visual ; tactile ; acoustic ; chemical

Food Habits

Oriental fire-bellied toads, like most frogs and toads, primarily perceive prey through movement. They wait patiently for their prey to draw near and then pounce quickly to capture the prey. As larvae, Oriental fire-bellied toads consume algae, fungi, detritus, plants, and protozoans. As adults, their diet consists of terrestrial invertebrates, including worms, molluscs, and insects. (Kuzmin and Vredenburg, 2003)

Primary Diet
carnivore (Insectivore , Molluscivore )

Animal Foods
insects; terrestrial non-insect arthropods; mollusks; terrestrial worms

Plant Foods
algae

Other Foods
fungus; detritus ; microbes

Predation

Known Predators
  • larger, predatory birds (Aves)


The main predators of Bombina orientalis are birds and larger aquatic animals. Oriental fire-bellied toads are poisonous to eat and, when threatened, they exhibit a posture known as unkenreflex. They flip on their backs and arch their spines. The brilliant warning spots on their underside warn potential predators of their toxicity and may deter predation. Their dull-colored back provides perfect camouflage to blend in with the muddy waters they inhabit. ("The Oriental Fire-bellied Toad", 2004; Kuzmin and Vredenburg, 2003)

Anti-predator Adaptations
aposematic ; cryptic

Ecosystem Roles

Oriental fire-bellied toads prey upon terrestrial invertebrates and are also preyed on by bird species and larger aquatic animals.

Economic Importance for Humans: Positive

Bombina orientalis is a popular toad species in the exotic pet trade. They are hardy animals with long lifespans. (Miller, 2002)

Positive Impacts
pet trade

Economic Importance for Humans: Negative

Bombina orientalis is a poisonous species, although are popular as pets. Their skin toxin is not poisonous to human skin, but is harmful when rubbed in the eyes, mouth, or on broken skin. Hands should be washed thoroughly before and after handling. Handling oriental fire-bellied toads can result in itchy eyes and a runny nose. (Miller, 2002)

Negative Impacts
injures humans (poisonous )

Conservation Status

IUCN Red List of Threatened Species [Link]
Least Concern
More Information

US Federal List [Link]
No special status

CITES [Link]
No special status

Bombina orientalis is not currently considered a threatened species. (China Species Information System, 2003; Kuzmin and Vredenburg, 2003; Miller, 2002)

Other Comments

In cases of extreme danger, Bombina orientalis can excrete so much poison that its entire body becomes covered in a soapy foam. ()

For More Information

Find Bombina orientalis information at

Contributors

Tanya Dewey (editor), Animal Diversity Web, University of Michigan Museum of Zoology.

Todd Szcodronski (author), University of Michigan, Phil Myers (editor), Museum of Zoology, University of Michigan.

References

Hogle Zoo. 2004. "The Oriental Fire-bellied Toad" (On-line). Accessed August 30, 2004 at http://hoglezoo.org/animals/view.php?id=201.

China Species Information System, 2003. "China Species Information System" (On-line ). Accessed 03/19/03 at http://www.chinabiodiversity.com/search/english/detail.shtm?cspcode=040130005.

Hickman, c., L. Roberts, A. Larson. 2003. Animal Diversity. New York, NY: McGraw Hill.

Kaplan, R. 1992. Greater Maternal Investment Can Decrease Offspring Survival In The Frog Bombina Orientalis. Ecology, 73/1: 280-288. Accessed March 18, 2003 at http://www.jstor.org/view/00129658/di960342/96p0091u/.

Kuzmin, S., V. Vredenburg. 2003. "Bombina orientalis" (On-line). Amphibiaweb. Accessed March 16, 2003 at http://www.amphibiaweb.org/cgi-bin/amphib_query?query_src=aw_lists_genera_&table=amphib&where-genus=Bombina&where-species=orientalis.

Miller, J. 2002. "Oriental Fire Bellied Toad" (On-line). Living Underworld. Accessed March 14, 2003 at http://www.livingunderworld.org/anura/database/bombinatoridae/bombina/.

Staniszewski, M. 1998. "Marc Staniszewski's Amphibian Information Center" (On-line ). The Fire Bellied Toad (Bombina species). Accessed 03/16/03 at http://www.amphibian.co.uk/bombina.html.

To cite this page: Szcodronski, T. 2006. "Bombina orientalis" (On-line), Animal Diversity Web. Accessed May 31, 2012 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Bombina_orientalis.html

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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